- i ele i eh Sree ePTas er
> Ph 1% er . "8 Kah Pen ie 5 thal te 4 PO rere ie:
papsccrorongrorrenertiseareselees fe | AS, Stes
pets ts 4 A . se 5 cd as i
sie siite vieeete | | 8
i ; ~ 3 Ae Ae ‘ t - m s : y ’ : 7 “e re) é +
ait eters f i : 3 de ae ar sd Sa? rercletefaga a i 4 4 ae? e
"e ‘ ab ah rf 4 a i fefeqe POI e Th eta OTe Te? nee: os
rf eis rarers ere ore * ed S ¢ 8 rareperere Srerey ere. ree oie hap
rererereetres re ri as ~4 Siopalerorerdivre ters
re} : eae Te FA? he eae tee) - e% eth edhd at eke hho , yer
pats wt cape ee : cists? 4 4
eh - ti i eo ik eh Fe hg oF . = , ere! or ' * > ep
: weit vei a eR hdrw Pat a bse aperere repotor gous parerers a ded hththtes rere relarercre
Te ; “ ’
4 SPeTOrare rhe Pea rate
Sretesire Seat Se je
‘ Pores : ey
athe praretere -
Thiers Peery by ? soe
; Fo garda igs: ; rahe aierere
inven, ; Spe rere ree Serererst ere he Ba - “4
rte Sbload gh Me 3
ei = ; j ha! Paras . Fare
ba
Ad ; » Ha eal r :
j nee . pion Ljadadatetaar tino
‘ rer ek te
er abharae
Ve eer
Rah hittin oiee nda wapepepere) : CHR Sr es teteye yes dt inh sex oti oh ne bs Pea Need A, erer WIR er eta rare:
‘ j ‘ wet i i oF ue rn ree : f iets : ee I> Srerene re
: areata e Spiaieee ss epee eiitaherarer,
ednc8 hs
aadeee 2
ein gts
PCTS Tere ererct
apare rete
eee: sean
PE
Pele rere
hehe ters :
Hi na a nach han Tata ee
ie tharetiate te te
=e in aah eo
: Sa
STP Tele
si mat natant lee ed bo « ited. Z vp 22
Rght te tena yor rete re Paths jerpretbes
TC NST RNS perce eRe See res a 4 SAA ee Atos ; = =
4 b POP TENS wee: :
hah Meath wechk le tees oF WOE PED
Sane hee ce
Leake oe
Oe SHR ee meee
we weer
wre ree: J
ee eee ee ee we
ik Ae Ge
NFO et eee
eae Jedd eats bas Ay, heathen. okies - » , cies a
: Jedi, Said mabe aie - ° Peta A Ne eet
‘ Ong STW Pe stig
oe ce aie es
oe ee me
As
SWE Sgt ig WA SAT
nt itneem baht ah ok Te ok
apenas Pies 15 ae, - + 5 ee J abe ah
: wa A lett mo, “: . E Rot > : a ent et Pe aes : ° -
é : r RSet : : . : blight Shh tet ae a eee
SPE EAE See eer eee r
] : t ; eh ene Sis Sanna ee Pp ae Nene
‘ere yf
ae EE NETO aoe ee pam a ey ° rere ee ere > 3 E a prune
ST PT OTE, rere ere cae . es tee i ad te - Ske 2s Nae fps Wie taco teasers ee o> * POPWiele whee tere eae ~ : ~ Sere > Py SESE TS
Dak liek eae oe eld iol ° cies we ere ay ary z hthalaaae r ites aR Rabie eae ee hie a» Baie E Sr irk Se taba talk Rete es or ae é daa Ath th eh R ch dk hed ka te ee
on : ae pee man Sree Fee Tere ere eS
oS ee
fate a i
iweb Be vgs Pe
> i ee f di
4 i I
Dey ; y
ier a, oily (om at ar : i ae Coe Bad :
Aer fee 7 Fx ne em ; ‘eee te a)
Ty * ae i i waif J : dit a. ' 7 2 a a ¥ ao i
in .
os
y
J
Britt
’ jeu Mi
ae ite As
id 4 A fad
of) eS! i
e i: te
f
4,
,
fy ba
tt
Contributions
of the
American Entomological Institute,
Volume 19, 1982-1983
. Gupta, Virendra. A revision of the genus Delomerista
(Hymenoptera: Ichneumonidae). 42 pp. Sept. 1, 1982.
. Gupta, Santosh. A revision of the genus Agonocryptus
(Hymenoptera: Ichneumonidae). 45 pp. Sept. 1, 1982.
. Gupta, Santosh. A review of the genus Cryptohelco-
stizus (Hymenoptera: Ichneumonidae). 11 pp.
Sept. 1, 1982.
. Gupta, Virendra. A review of the genus Perithous
with descriptions of new taxa (Hymenoptera: Ichneumon-
idae). 20 pages. Sept. 1, 1982.
. Gupta, Virendra. A study of the genus Hybomischos
(Hymenoptera: Ichneumonidae). 5 pp. Sept. 1, 1982.
. Howden, Anne T. Revision of the New World genus
Hadromeropsis Pierce (Coleoptera, Curculionidae,
Series 93 180 pages. November 30, 1982.
. Gupta, Virendra. The ichneumonid parasites associ-
ated with the gypsy moth (Lymantria dispar). 186 pp.
February 22, 1983.
. Sabrosky, Curtis W. A synopsis of the world species
of Desmometopa Loew (Diptera, Milichiidae). 69 pp.
August 15, 1983.
Contributions
of the
American Entomological Institute
Vol. 19, Parts 1-5, 1982
Xe
1. Virendra Gupta. A revision of the genus Delomervista
(Hymenoptera: Ichneumonidae). 42 pages.
2. Santosh Gupta. A revision of the genus Agonocryptus
(Hymenoptera: Ichneumonidae). 45 pages.
3. Santosh Gupta. A review of the genus Cryptohelcostizus
(Hymenoptera: Ichneumonidae). 11 pages.
4. Virendra Gupta. A review of the genus Perithous, with
descriptions of new taxa (Hym.: Ichneumonidae). 20 pages.
0. Virendra Gupta. A study of the genus Hybomischos
(Hymenoptera: Ichneumonidae). 5 pages.
A REVISION OF THE GENUS DELOMERISTA
(HYMENOPTERA: ICHNEUMONIDAE)
Virendra Gupta
Center for Parasitic Hymenoptera
Department of Entomology and Nematology
University of Florida, Gainesville, FL 32611
Delomerista Foerster belongs to the Tribe Theroniini, subfamily
Pimplinae (=Ephialtinae). Some authors tend to place it in a different tribe
Delomeristini, but as Carlson (1979) has stated, there is really no evidence of
its relationship either way, and therefore it is here left within the tribe
Theroniini, as it is placed by Townes (1969).
Delomerista is a moderate-sized genus of Holarctic distribution. Species
of it parasitise saw-fly cocoons, though in literature there are records of
their being parasitic upon lepidopterous hosts as well as ona weevil. More
recent studies on the genus are those of Walkley (1960) on the North American
species and of Kasparyan (1977) on the European species. Additional species
have been discovered from India, Europe, and North America in the collections
of Townes, Gupta, Canadian National Collection, and of the U. S. National
Museum. Some of the American species appeared to have previously been
mixed up. Types and authentic determined specimens of several European,
Japanese and American species were studied to elucidate their taxonomic rela-
tionships and identities. This resulted in the recognition of several new spe-
cies which occur sympatrically with common species like D. noviia, borealis,
etc. and were previously mixed up with them, in the separation of D. japonica
and D. diprionis as valid species, and the discovery of D. indica, n. sp., from
the Himalayan mountains of India. D. indica extends the range of the genus to
India.
A total of 17 species and 4 subspecies are now recognized, of which 6 taxa
are new to science.
Genus DELOMERISTA Foerster
Delomerista Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 164.
Type-species: Pimpla mandibularis Gravenhorst; designated by
Schmiedeknecht, 1888.
Taxonomy: Walkley, 1960: 362-372. Townes, 1969: 127. Kasparyan,
1977: 69-74.
Biology: Morris, etal., 1937: 360-361.
Body black. Face and clypeus of male yellowish-white (except in laevis).
Moderately slender, medium-sized species. Face a little convex and minutely
to moderately strongly punctate. Scape punctate. Clypeus usually lighter
colored than face, flat (convex in D, laevis), its apical margin concave and
without a median tooth. Mandibular teeth equal. Malar space 0.29 to 1.0 the
basal width of mandible, yellow. In males malar space correspondingly shorter
than infemales. Flagellar segments with linear sensillae which are often ab-
sent on the basal one or two segments. Thorax usually subpolished and with
: Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
minute setiferous punctures. Notauli indicated anteriorly. Epomia present.
Prepectal carina present. Propodeum areolated, both longitudinal as well as
transverse carinae present, but only the carinae bordering areola and petiolar
areas prominent. Costula present or absent, or indistinct and its place indi-
cated by the different sculpture of first and second lateral areas; second lateral
area often somewhat depressed and rough. Apical transverse carina almost
circular and more prominent. Tarsal claws simple, of moderate size, without
an enlarged bristle having a spatulate tip (cf. Theronia), though a long slender
bristle present on each claw. Nervellus intercepted variously, at, above or
below the middle (even varying within the same species). Abdomen strongly
granulose, granuloso-mat, or coriaceous with small scattered hairs, or closely
punctate (as in two species pfankuchi and kusuoi). First tergite with a weak to
strong dorsal curvature. Median carinae usually ending at this dorsal hump.
Lateral carina passing just above the spiracle and often weak at this point.
Ovipositor moderately compressed, moderately long (0.7 to 1.0 the length of
abdomen), or very long (2.0 the abdomen in longicauda), its tip not sinuate but
variously modified, either nodiform, or upper valve thick, or upper valve
occupying a greater part of the depth of ovipositor tip (figs. 47-49, 51-53).
The apical slope of the upper valve also variable and of diagnostic value for
species.
HOST ASSOCIATIONS
Species of Delomerista seem to be chiefly ectoparasitic on pupating sawfly
larvae within the cocoons. Host records of many species are lacking, while
some species have been reported ectoparasitic upon a variety of lepidopterous
larvae, and even a weevil larva (Vononychusi vulpeculus for D. novita). Aubert
(1969), quoting Kolomiets, 1962) even mentions D. mandibularis as being hyper-
parasitic upon larvae of Rhogas dendrolimi Matsumura, through Dendrolimus
sibirvicus. Most authors, however, believe that all hosts other than sawfly
hosts are probably erroneous, as they are not confirmed by subsequent rear-
ing records. For the same reason, Walkley (1960) stated that it is unwise to
disregard the host records from Lepidoptera and Coleoptera until further rear-
ings are done.
LARVAL MORPHOLOGY
(Figs. 63-65)
The Larvae of Delomervista have a large tooth-like projection at the junction
of the blade and base of mandible. According to Short (1978) this character is
found among other genera of the Theronini,in the Rhyssini, certain Ephialtini,
and in the Orthopelmatinae. The epistoma is incomplete, hypostoma and
hypostomal spur well sclerotized, lateral parts of labial sclerite slender and
ventral part broad, about twice as deep as the width of lateral part. Maxillary
and labial palps flattened and disc-shaped. Labral sclerite complete. Man-
dible with a broad base and its blade bifurcated—the longer part with dorsal
and ventral teeth and smaller part toothless. Maxillary and labial palps with
two sensillae each. Closing apparatus of spiracle not adjoining atrium. Anten-
na papiliform. Length of skin setae equal to the larger toothed part of mandi-
bular blade.
Short does not separate out Delomeristini from Theroniini.
V. Gupta: Genus Delomerista (Ichneumonidae) 3
SPECIES
A list of species so far known, together with their host associations as far
as known, is given below, including the new taxa described in the text. Species
no longer valid, nor belonging to Delomervisia are placed within brackets [| ].
Only valid species are numbered.
Four species groups are recognized, chiefly on the nature of the ovipositor
tip. They are the Novita Group, the Japonica Group, the Frigida Group, and
the Mandibularis Group. They are characterized and keyed in the key that fol-
lows the species list. The figures of the ovipositors should help identify the
species-groups as well as the species.
| Ephialtes albicinctus Desvignes, 1862]. Type °%, ?Great Britain (London).
Name preoccupied. A synonym of Delomerista mandibularis Graven-
horst cf. Fitton (1978).
?Great Britain. Host: Unknown.
| Pimpla bilineata Brulle, 1846]. Type 2, Algeria (Paris).
Oehlke (1967) synonymized it under Coccygomimus contemplator
(Mueller) with a query, but Aubert (1969) placed it under Delomervista.
The latter situation followed by Constantineanu & Pisica (1977).
According to original description, apparently a species of Coccygomi-
mus.
Algeria. Host: Unknown.
Delomerista borealis Walkley, 1960. Type ¢, N.W.T. (Washington).
Also reported from Alaska and Quebec by Walkley.
Aubert (1969) placed it under D. mandibularis with a query. Kasparyan
(1977) reported it from the European USSR. |
A valid species belonging to the Novita Group.
Occurring in Northwestern parts of North America and European USSR.
Host: Unknown,
[Ephialtes desvignesii Marshall, 1870]. New name for E. albicinctus
Desvignes, 1862.
Oehlke (1967) placed it under Delomerisia. Fitton (1978) placed it asa
synonym of D,. mandibularis (Gravenhorst).
England. Host: Unknown.
Delomerista diprionis Cushman, 1939. Type ¢, Ontario, Canada
(Washington).
Walkley (1960) synonymized it under D. japonica Cushman.
Hereby considered as a valid species, belonging to the Japonica Group.
Nearctic. Hosts: Several species of Diprion, Neodriprion and Gilpina,
including D, similis, N. lecontei, N. nanulus nanulus, N. pratti
banksianae, N, sertifer, N. tsugae, Gilpina frutetorum, and
G. hercyniae.
Delomerista excavata Ulbricht, 1913. Type 2, Germany (?).
Aubert placed it under mandibularis with a query, while other authors
are not certain about its identity.
4, Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
The type could not be located and therefore its taxonomic identity could
not be ascertained.
Germany. Host: Unknown.
4. Delomerista frigida Kasparyan, 1977. Type 2, European USSR (Leningrad).
Belongs to the Frigida Group.
Eastern Palaearctic. Host: Unknown.
[Delomerista gelida Walkley, 1960]. Type ?, N.W.T. (Washington).
Hereby synonymized under D, mandibularis Gravenhorst. N. SYN.
Nearctic. Host: Unknown.
9. Delomerista indica Gupta, new species. Type 2, Himalaya: Dalhousie
(Gupta).
Belongs to the Japonica Group.
India (Himalayan mountains). Host: Unknown.
6. Delomerista japonica Cushman, 1937. Type 2, Japan (Washington).
Walkley (1960) synonymized D. diprionis Cushman under it, but both
species are here considered distinct but related, belonging to the
Japonica Group.
Japan. Host: Diprion nipponicus.
1. Delomerista kusuoi Uchida & Momoi, 1957. Type 2, Japan (Sapporo).
A valid species related to D. pfankuchi and belonging to the Novita
Group.
Japan. Host: Unknown.
[Pimpla laevifrons Thomson, 1877]. Type “, Germany (Lund).
Townes (1944) synonymized it under D, texana (Cresson), while Oehlke
(1966) synonymized texana under laevis (Gravenhorst).
Aubert (1969) considered it distinct and synonymized stvandi Ulbricht
under it. Constantineanu and Pisica (1977) treated it as a separate
species. Kasparyan (1977) studied the lectotypes of laevis and laevi-
frons and confirmed the synonymy of this species. D, stvandi is nota
synonym of it, though a cotype of it is conspecific with it. The lectotype
of stvandi is different.
Europe. Host: Unknown.
8. Pimpla laevis Gravenhorst, 1829. Type 2, Italy (Wroclaw).
=laevifrons Thomson.
=texana Cresson (cf. Oehlke, 1966).
A cotype of D. strandi belongs here, which is different from the lecto-
type of strandi designated by Oehlke, 1967.
A valid species, belonging to the Mandibularis Group.
Holarctic. Hosts: Rhyacionia buoliana (Lep.: Tortricidae) in Europe
(cf. Aubert). Carlson (1979) does not mention any host in North
America.
9. Delomerista lepteces Walkley, 1960. Type ¢, Alaska (Washington).
Belongs to the Novita Group.
Nearctic. Host: Unknown.
V. Gupta: Genus Delomerista (Ichneumonidae) 5
10. Delomerista longicauda Kasparyan, 1973. Type 2, Russia (Leningrad).
A species belonging to the Mandibularis Group. A subspecies of it
(longicauda americana) is described from Northern Nearctic.
Holarctic. Host: Unknown.
11. Pimpla mandibularis Gravenhorst, 1829. Lectotype 2, Poland (Wroclaw).
= albicinctus Desvignes (cf. Fitton, 1978)
= desvignesii Marshall (cf. Fitton, 1978)
= gelida Walkley (new synonym).
Aubert (1969) placed excavata Ulbricht as a synonym of it with a query,
but Kasparyan (1977) did not confirm this synonymy. He also placed
D. borealis Walkley as a doubtful synonym of it, apparently after the
suggestion of Walkley herself, which was because of misdetermined
specimens of mandibulavis in Washington. In Washington there are
specimens from Europe determined as mandibularis by Roman and
Heinrich, which are specifically identical with the specimens of borealis
Walkley, but not with specimens determined as mandibularis by Perkins
and Kasparyan.
According to Oehlke (1967), Perkins selected a lectotype in 1936 and so
labelled the specimen, which was subsequently designated lectotype by
Oehlke (1967). Kasparyan (1977) followed this interpretation. Oehlke
mentions Breslau, Poland as the lectotype locality, while Kasparyan
mentions Warmbrunn, Poland!
A valid species belonging to the Mandibularis Group.
Hosts: As mentioned by Aubert from Europe: Strongylogaster sp.,
Euuva amerinae (Hym.: Tenthredinidae).
12. Delomerista masoni Gupta, new species. Type 2, Michigan (Townes).
Belongs to the Mandibularis Group.
Nearctic. Host: Unknown.
13. Pimpla novita Cresson, 1870. Type, Mass. (Philadelphia).
Kasparyan (1977) reported it from European USSR.
A valid species belonging to the Novita Group. A new subspecies of it
(novita europa) is described from Poland and Kasparyan's specimens
may belong to the European subspecies.
Holarctic. Hosts: Mononychus vulpeculus (Curculionidae), Acrobasis
rubrifasciella, Acrobasis spp., Exartema olivaceanum, Eublemma
minima (= Thalpochares carmelita) (Lepidoptera). Macremphytes sp.,
Diprion similis (Hymenoptera).
14. Delomerista pfankuchi Brauns, 1905. Type 2, Bremen (Berlin).
Troctocerus unicolor Hedwig, 1959. Syn. by Horstmann, 1981.
Europe. Russia. Walkley (1960) reported it as 'Probably America",
but it does not occur in the Nearctic Region.
Valid species belonging to Novita Group.
Palaearctic. Hosts: Chionodes tragicella, Psyche viciella, Talaeporia
tubolosa, and Diplodoma marginepunctella (Lepidoptera). Diprion pini
(Hymenoptera).
15. Pimpla strandi Ulbricht, 1911. Lectotype 2, Norvegia (Berlin).
Lectotype designated by Oehlke, 1967.
Another cotype conspecific with laevifrons and so labelled by Aubert,
6 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
led him to consider the two synonymous.
A valid species, also occurring in the Nearctic Region. Belongs to the
Mandibularis Group.
Holarctic. Host: Unknown.
[Pimpla texana Cresson, 1870]. Type 2, Texas (Philadelphia).
P. laevifrons considered as a synonym of it by Townes (1944), while
Oehlke (1966) synonymized it under /aevis (Gravenhorst).
A synonym of Delomervista laevis. 7
Nearctic. Host: Unknown.
16. Delomerista townesorum Gupta, new species. Type 9, Michigan (Townes).
Belongs to the Frigida Group. |
Nearctic. Host: Unknown.
[Troctocerus unicolor Hedwig, 1959]. Holotype ¢, "Paitzkofen b. Straubing.
A junior synonym of Delomerista pfankuchi, vide Horstmann, 1981.
17. Delomerista wakleyae Gupta, new species. Type 9, Alaska (Townes).
Belongs to the Frigida Group.
Nearctic. Host: Unknown.
MALES
The matching of the males with the females has posed a problem, as most
males available look alike and apparently males of several species are unknown.
Attempts have been made to identify the males in association with the females.
This resulted in certain broad groupings. These groupings are described below
and should aid in the identification of the males.
I. Males with face black, yellow only on sides. Malar space long, 0.8 to
1.0 the basal width of mandible. Clypeus convex. Abdominal tergites finely
granular. Only one species, Delomerista laevis, belongs here.
All other males so far as are known, have face yellowish-white, or white,
malar space 0.2 to 0.33 the basal width of mandible, and clypeus flat.
II. Areola small, broadly triangular due to the apical transverse carina
being close to the middle of propodeum. Propodeum short, sloping from base
to apex. Apical transverse carina often the strongest and very convexly arched.
This group includes the males of the Japonica Group, D. japonica, diprionis,
and indica, all of which have yellow malar space, tegula and ventral aspects of
scape and pedicel. D. diprionis has the strongest apical transverse carina,
which even encroaches the basal half of propodeum.
III. Propodeum smooth and shiny, with areola horse-shoe shaped, not
elongate. Costula distinct. Propodeal carinae rather strong and sharp.
Malar space, scape and pedicel ventrally, and tegula yellow. Flagellum
brownish. Propodeum with a short dorsal face. Hind femur usually wholly
brownish-yellow. Includes D. masoni of the Mandibularis Group.
IV. Areola elongate. Costula indistinct to absent. Propodeum long,
smoother, or granulose laterally. Apical transverse carina of propodeum
V. Gupta: Genus Delomerista (Ichneumonidae) é
usually in apical 0.3 of propodeum. Dorsal face of propodeum long and not
sloping. Propodeum sloping only apicad of transverse carina. The rest of the
known males belong here.
A. Tegula black. Scape and pedicel black. Delomerista borealis belongs
here.
B. Tegula yellow. Malar space black. Three species, D, novita, longi-
cauda and lepteces belong here. In D. novita, the scape and pedicel are yellow
ventrally, malar space short, 0.2 the basal width of mandible, nervellus inter-
cepted at lower 0.4, face as long as wide, fore and middle coxae generally
white, and hind femur short, compressed and largely reddish. In D. longi-
cauda americana (male of nominate subspecies unknown), the scape and pedicel
are black, malar space 0.33 the basal width of mandible, nervellus intercepted
at lower 0.3, face wider, about 1.5 as wide as long, shiny, fore coxa alone
white, and hind femur normal, largely to wholly blackish or blackish-brown.
D, lepteces is very much like D, longicauda, but malar space 0.3 as long as
basal width of mandible, face 1.3 as wide as long, dull, and hind femur is
largely reddish-brown or reddish, except in apical 0.3.
C. Tegula yellow. Malar space yellow. Delomevista townesorum and
D. mandibularis belong here. Both these species show variations in the colora-
tion of scape, pedicel, and in the markings on the femora.
D. townesorum has a rugulose, rectangular face, hind femur with a black
apical ring, and nervellus intercepted at its lower 0.4 to 0.45 (appears usually
in the middle).
D, mandibularis generally has a smoother, squarish face, hind femur
usually wholly orange-brown, and nervellus intercepted in the lower 0.3 to
0.35. The scape and pedicel are usually yellow ventrally. There are varia-
tions, however. Some males have a rugulose face and scape appears partly to
largely black. A large number of males from British Columbia in Townes
Collection are tentatively placed here. They may be different.
V. Abdomen rugoso-punctate. The male of D. pfankuchi has a rugoso-
punctate abdomen, like that in female (all other males have coriaceous
abdomen), scape and pedicel yellow ventrally, flagellum brownish and hind
femur wholly orange colored.
In the key that follows, only the females have been taken into consideration.
D, excavata Ulbricht is unknown to me and therefore not included in the key,
nor in the text.
KEY TO THE SPECIES GROUPS AND SPECIES OF DELOMERISTA
(Females only. Delomerista excavata Ulbricht excluded)
1. Ovipositor with a distinct subapical node whence it tapers gradually to a
point (figs. 3,6,9). Ventral margin of upper valve of ovipositor con-
cave subapically where the lower valve widened and occupying the
greater part of the depth of the ovipositor. Basal ridges on lower valve
strongly inclined and rest of the ridges somewhat sinuate. Basal two
flagellar segments with several rows of sensillae (cf. Frigida Group)
(figs. 12,15,18,19,20). (In one species, lepteces, ovipositor finely
tapered and needle-like, fig. 16). A. The Novita Group....... 4
8 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Ovipositor tip not nodiform, a little bulbous or more conspicuously
widened (often a few low ripples seen in profile on the upper valve,
figs. 23,28). Upper valve heavier or wider preapically than the lower
valve and occupying the greater part of the preapical depth of ovipositor.
Ventral margin of upper valve convex. Ridges on lower valve (except
the basal 3-4) almost vertical to reclining... .% )...6 .4.508. 6. 2
2. Upper valve of ovipositor not unusually heavy or widened, with an even
gradual slope and with one or two ripple-like preapical formations
(figs. 23,28). Ridges on lower valve vertical (except the basal ones).
First flagellar segment almost devoid of sensillae or only one or two
present. II segment with fewer sensillae. (This group is sympatric
with the Novita Group and the American species of it have been mixed
up with the species of the latter. The ovipositor looks somewhat
similar, but is definitely not nodiform and is a little bulbous in outline
and sensillae are virtually absent). Propodeum with a flat dorsal face
and then sloping only in apical half. B. The Frigida Group..... 8
Upper valve of ovipositor heavier and widened preapically, bulbous or with
a short abrupt apical slope (figs. 33, 38,39, 44, 47-49, 51-53). Apical
ridges on lower valve vertical to reclining. Sensillae on basal two
flagellar segments numerous or sometimes fewer in number. Propode-
um sloping from base to apex, though sometimes basal part convex
(igs. 40,90, 98 a ae i ee 3
3. Upper valve of ovipositor bulbous in outline, widened preapically and then
abruptly sloping (figs. 33,38, 39,44), with faint ripples. Apical ridges
on lower valve reclining while the basal ones inclining. The two valves
meeting almost ina straight line: this line at mid height of ovipositor
at base and usually faint. Basal two flagellar segments with numerous
sensillae (figs. 31, 32, 36,37,45,46). Propodeum in profile view with
an even slope from base to apex (fig. 40).c, The Japonica Group. 10
Upper valve of ovipositor rather heavy, and occupying the greater part of
the depth of ovipositor (figs. 47-49, 51-53), and without or with only
faint ripples. Apical slope abrupt, short, except in longicauda (fig. 53),
where ovipositor 2.0 as long as abdomen. Ovipositor usually arched.
Ridges on lower valve vertical to slightly inclined (basal 3 ridges
strongly inclined). The two valves meeting along an arched line, which
is conspicuous throughout the length of ovipositor and is above the mid-
height at base of ovipositor. Basal two flagellar segments with fewer
sensillae (fig. 59-60).Propodeum in profile view (figs. 50, 54) strongly
convex basally and then abruptly sloping to apex.
D. The Mandiputarie Grou. 3. 2 a a ee 12
(The Novita Group)
4. Abdomen closely punctate (figs. 5,11). Apical margins of tergites banded
with yellow or red. Malar space 0.25 the basal width of mandible.
Propodeum subpolished and with a few scattered punctures to punctate
(figs. 4,10). Costula faint to distinct.
Abdomen granulose to granuloso-coriaceous (figs. 2, 8,14), without apical
pale bands on tergites. Malar space 0.3 to 0.5 the basal width of man-
dible. Propodeum polished to subpolished. Costula absent. .... 6
V. Gupta : Genus Delomerista (Ichneumonidae) 9
Propodeum (fig. 4) subpolished, with a few scattered punctures laterally.
Costula very faintly indicated. Abdominal tergites with yellow apical
bands. Nervellus intercepted below the middle. Palaearctic.
4. pfankuchi Brauns (p. |5)
Propodeum (fig. 10) punctate, second lateral area rugoso-punctate.
Costula distinct. Abdominal tergites apically banded with red and punc-
tation coarser than in pfankuchi (fig. 11). Nervellus intercepted at its
middle. Japan. -o4 20a Sos, 5. kusuoi Uchida & Momoi (p. 18)
Ovipositor finely tapered apically, needle-like (fig. 16), nodus rather
indistinct. Malar space 0.45-0.5 the basal width of mandible.
Propodeal areola (fig. 13) horse-shoe shaped. Nearctic.
3. lepteces Walkley (p. 15)
Ovipositor typical for the group with a distinct node and then long tapering
(figs. 3,9). Malar space 0.3-0.45 the basal width of mandible.
Propodeal areola usually elongate, more strongly defined and pentagon-
BLAS LOR Te eS ee
Tegula yellow. Hind tibia yellow ventrally or at base. Hind tarsus basally
yellow. Abdomen granuloso-coriaceous (fig. 2). Malar space 0.3 the
basal width of mandible. Nervellus intercepted at: its lower 0.3-0.4.
Holaveties 1 0- ae P 1. novita (Cresson) (p. 11)
Tegula black. Hind tibia and tarsus wholly black. Abdomen granulose
(fig. 8). Malar space 0.4-0.45 the basal width of mandible. Nervellus
intercepted at its lower 0.4-0.45. Holarctic. |
2. borealis Walkley (p. 14)
(The Frigida Group)
Face granuloso-punctate medially. Tegula black. Tergite I convex,
granulose laterally, its dorsal and lateral carinae weak and confined only
along the basal declivity. Fore leg wholly reddish-brown. Europe.
6. frigida Kasparyan (p. 18)
Face subpolished, with or without fine punctures. Tegula black or yellow.
Tergite I flattened laterally and more rugulose rather than granulose,
its median and lateral carinae distinct. Fore leg with yellow ventral
mia NOVUT AMOR Cain Ok I ee re we WH ee a 9
Tegula black. Propodeum rugulose in pleural area, second lateral area
and in petiolar area. Legs dark reddish-brown with fore leg brownish
(except rarely). Malar space 0.5 the basal width of mandible. Ovi-
positor long, a little up-curved and longer than abdomen. Abdomen
granuiose, Nearetios <r. oo worn 7. walkleyae, n. sp. (p. 18)
Tegula yellow. Propodeum smoother to subpolished, particularly in
lateral and petiolar areas. Legs light yellowish-brown. Malar space
0.3-0.4 the basal width of mandible. Ovipositor as long as abdomen,
usually straight. Abdomen granuloso-mat (finer than in walkleyae).
Nearotion. i 6480 5> CRO RB PN 8. townesorum, n. sp. (p. 19)
10
10.
11.
12.
13.
14.
Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
(The Japonica Group)
Ovipositor tip a little swollen preapically and then abruptly sloping (short
taper, fig. 33,39). First abdominal tergite thinner in profile view,
its dorsomedian carinae angled at 30° and with a conspicuous flange at
its junction with lateral carina. Basal declivity smoother and shiny.
Postpetiole flat and rugulose. Malar space 0.33 to 0.45 the basal
width of mandible. Eastern Palaearctic: Japan, USSR.
10. japonica Cushman (p. 22)
Ovipositor tip in profile view more parallel-sided, with a small convex
slope (figs. 38,44). First tergite convexly arched, its median carinae
moderately raised and making an angle of 45° with the horizontal axis,
not conspicuously flanged at base. Malar space 0.5-0.7 the basal
WAGE OL MIAMI NAle. He SA ee Se ee. Melinda. Soni eg eel
Malar space 0.6-0.7 the basal width of mandible. Nervellus intercepted
below the middle (lower 0.33). Junction of median and lateral carinae
of first tergite not flanged, the lateral carina angled at spiracle and
usually erased there or apically. Basal declivity of first tergite dull.
Ovipositor tip as in fig. 38. Nearctic. .9. diprionis Cushman (p. 20)
Malar space 0.5 the basal width of mandible. Nervellus usually inter-
cepted at the middle (some exhibit variations 0.5 +0.15). Junction of
median and lateral carinae of first tergites moderately flanged, the
lateral carina complete and strong, arched at spiracle. Basal declivity
of first tergite rough. Ovipositor as infig. 44. India.
i 11. indica, n. sp. (p. 23)
(The Mandibularis Group)
Malar space about as long as or longer than basal width of mandible (0.8 in
o). Clypeus convex. Face smooth (face of male black). Propodeum
largely granulose. Abdominal tergites finely granulose (shagreened in
%). Ovipositor tip as in fig. 52. Holarctic. |
15. laevis (Gravenhorst) (p. 28)
Malar space 0.4-0.6 the basal width of mandible. Clypeus flat. Face with
Minute punctures, SUDNOMeN ed... i. ve vette ets Ge dake aS RA le 13
Ovipositor very long, longer than the body and about 2.0 the length of
abdomen. Ovipositor tip upcurved, narrowed preapically (fig. 53).
PGlAveties. si utite Peewee AO) 16. longicauda Kasparyan (p. 29)
Ovipositor shorter, only about as long as abdomen or shorter, straight
preavically and.not- nNavrowed, Fo ok wa Me CORE 14
Ovipositor almost parallel-sided in profile view, uniformly slightly arched
upwards, particularly near tip, not conspicuously widened preapically
(fig. 48,49). First flagellar segment almost devoid of sensillae
(fig. 59) (one or two in a row sometimes present). Ovipositor as long
as abdomen. Holarctic. .. 12. mandibularis (Gravenhorst) (p. 24)
Ovipositor rather widened preapically (about 1: 1.5) (figs.- 47,51, 52) and
almost straight (or a little downcurved). First flagellar segment with
several rows of sensillae. Ovipositor shorter than abdomen. ... 15
V. Gupta: Genus Delomerista (Ichneumonidae) 11
15. Tegula black. Ovipositor very stout (fig. 47), slightly arched upwards.
Malar space 0.5 to 0.6 the basal width of mandible. Areola pentagonal
to a little elongate. Costula incomplete to indistinct. Second lateral
area of propodeum rugose and depressed. Head as wide as high.
Inner eye orbits shallowly indented. Holarctic.
13. strandi (Ulbricht) (p. 26)
Tegula yellow. Ovipositor moderately stout with a weak median bend down-
wards. Malar space 0.4-0.5 the basal width of mandible. Areola
semicircularly rounded, broader (sometimes elongate). Costula com-
plete and distinct. Second lateral area of propodeum shiny (sometimes
rugulose), generally not depressed. Head wider than high. Inner eye
orbits moderately indented. Nearctic. . . 14. masoni, n. sp. (p. 27)
A. THE NOVITA GROUP
Flagellum with sensillae, basal two flagellar segments with numerous
sensillae which are sometimes fewer in number.
Propodeum long, with a longer dorsal face. Propodeum dorsally smoother.
Areola elongate. Costula absent or faintly indicated (distinct in kusuoi, where
propodeum is somewhat punctate). Ovipositor tip nodiform, seen in profile
upper valve with a slight protuberance subapically whence it evenly tapers to
an apical point. At nodus, depth of upper and lower valves about equal; beyond
this point lower valve slightly encroaching upon the upper valve and lower
margin of upper valve concave. Ridges on lower valve (except the basal ones)
vertical and slightly sinuate. Ovipositor 0.8 to 1.2 as long as abdomen.
This group includes five species: D., pfankuchi from Europe, D. kusuoi
from Japan, D. lepteces from North America, and D. borealis and D. novita
from Europe as well as North America.
1. DELOMERISTA NOVITA (Cresson)
Female: Face convex, punctate in the middle. Clypeus flat. Malar space
0.3-0.33 the basal width of mandible. Head a little wider than long. Eye
moderately strongly notched a little above antennal socket. Frons smooth.
Vertex with minute setiferous punctures. Interocellar distance 0.6-0.7 the
ocellocular distance. First flagellar segment with linear sensillae. Second
and third segments also with linear sensillae. Sensillae on basal two flagellar
segments in novila europa fewer in number. Mesoscutum subpolished and
more hairy than other parts. Pronotum, mesopleurum and metapleurum shiny,
polished and with scattered hairs. Propodeum smooth dorsally and a little
punctate laterally and in pleural area, a little rough in the petiolar area.
Areola fully formed, but basal area and costula absent (fig. 1). Apical trans-
verse carina circular and strong. Dorsal face of propodeum appears flat and
about as long as its apical slope, which is gradual. Nervellus intercepted at
its lower 0.3-0.45. Abdomen granuloso-coriaceous (fig. 2). Ovipositor long,
straight, parallel-sided, about 0.5 as long as body and 0.8 as long as abdomen,
its tip with a subapical node and thence evenly and gradually tapered to a point.
Lower valve with vertical riges (fig. 3), with basal ridges inclined.
Male: Similar to the female but face smooth. Pleural area of propodeum
often rugulose. Propodeum dorsally flatter and more elongate and often with
minute punctures.
Two subspecies are recognized: Delomerista novita novita from North
12 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
America and D. novita europa from Europe. They differ as follows:
1. Sensillae on basal flagellar segments numerous. Areola generally hexagonal
and a little longer than wide (though in reared specimens variations are
seen from elongateM-shaped to somewhat broadly triangular). Legs
reddish-brown with fuscous and pale marks. Fore and middle tarsi
fuscous, their tibiae particularly the middle tibia, ventrally yellow and
with apical fuscous marks. Hind tibia largely yellowish-white ventrally.
Nexretio. 4.0.4 69, ees la. novita novita (Cresson) (p. 12)
Sensillae on basal two flagellarsegments fewer innumber. Areola usually
elongate, narrowed basally, and somewhat pentagonal. Legs more
uniformly brownish. Fore and middle tibiae and tarsi without fuscous
or pale marks. Hind tibia wholly brownish-black and only with a basal
white ring. Europe. ...... 2b. novita europa, n: subsp. (p. 13)
la. DELOMERISTA NOVITA NOVITA (Cresson) (figs. 1-3)
Pimpla novita Cresson, 1870. Trans. Amer. Ent. Soc., 3: 146. @. des.
Type ¥, Massachusetts (Philadelphia). Homotype examined in Townes
Coll., 1980.
Taxonomy: Walkley, 1960: 373. Kasparyan, 1977: 74. Carlson, 1979:
349.
Morphology: Finlayson, 1967: 1247 (larva). Short, 1978: 25,174 (larva).
Female: Basal flagellar segments with numerous sensillae. Areola gener-
ally hexagonal and a little longer than wide, but areola variable, particularly in
reared specimens, from elongate N-shaped to somewhat broad-triangular.
Black. Mandible, malar space, palpi, hind corner of pronotum, tegula,
and fore trochanter and trochantellus, yellowish-white. All coxae, femora,
and middle and hind trochanters and trochantellus reddish-brown, with fore
coxa often dark brown. Fore and middle tibiae reddish-brown, with their ven-
tral surface yellowish-white. Hind tibia with a yellowish-white annulus at
base, black dorsally, and yellowish-white ventrally, which mark variable, but
not extending to apex. Fore tarsus brown and middle and hind tarsi black.
Base of hind basitarsus white. Apical 0.22 of hind femur black. Sometimes
legs more uniformly reddish-brown, but hind tibia and tarsus exhibit the
characteristic pattern.
Male: Malar space 0.2 to 0.25 the basal width of mandible and black.
Face and clypeus white. Face subpolished, with scattered punctures. Scape
and pedicel white ventrally. Tegula yellowish-white. Fore and middle coxae
and trochanters white. Middle femur ventrally and middle tibia often wholly
white. Hind femur short, reddish-brown with a blackish mark in apical 0.25
to 0.4 and merging with the reddish color of femur. Sometimes fore leg darker
with coxa brownish.
One female labelled, 'Delomerista gracilis Cushman, Type", "No. 19179-
USNM", from Santa Cruz, California, is a variant specimen of novita novita
with legs more reddish-brown, areola triangular, dorsal face of propodeum
shorter, and apical transverse carina of propodeum more strongly arched.
Some reared specimens of novita novita from Wisconsin also exhibit this sort
of propodeum and a flatter first tergite.
Length: °, 9-183 mm. Fore wing 7-9.5 mm. Ovipositor 5-7 mm. ¢,
7-11 mm. Fore wing 4.5-8 mm.
Specimens: 29% males and 592, from the Nearctic Region: British
V. Gupta: Genus Delomerista (Ichneumonidae) 13
Columbia (Hudson Hope, Robson, and Stone Mt. Park); California (Santa Cruz
Mts.); Michigan (Ann Arbor, Brevort, Emmet Co., Huron Mts., Houghton Co.,
Iron River, Marquette Co., Schoolcraft Co., Roscommon Co.); Minnesota
(Stacy and Chisago Co.); New Hampshire (Mt. Madison, Pinkham Notch, and
White Mts.); New Jersey (High Point State Park); New York (Farmingdale,
Hancock, L. Sebago, Moss Lake, Oneota); North Carolina (Linville Falls);
Ontario (Bells Corners, Chaffeys Locks, Constance Bay, Cumberland, and
Ottawa); Oregon (Mt. Hood and Selma); Pennsylvania (Bald Eagle State Park,
Hamilton, Spring Brook), Quebec (Gracefield, Knowlton, Lacoste, Lac Mondor,
Cap Rouge, Gracefield, Ste Flore, and Sweetsburg); South Carolina (Cleveland);
Vermont (Laurel Lake); Virginia (Mountain Lake); West Virginia (Cranberry
Gls.); Wisconsin (Gibson Lake, Madison, and Polk Co.); and Yukon Territory
(Rampart House).
Specimens reported by Walkley (1960) from Saskatoona, Sask., Robson,
BC, and Golden Lake, Ontario, are now referred to Delomerista townesorum,
n. sp. Specimens reported by her from Maine, Maryland, Massachusetts,
Connecticut and Washington could not be examined.
Hosts: The host records on specimens seen are from Diprion similis at
Gibson Lake, Wisconsin, Stacy, Minnesota, and at Linville Falls, N.C., the
adults occur mostly during August. Walkley reported other host records
(quoting earlier authors), like Mononyhus vulpeculus, Acrobasis rubrifasciella,
Exartema oliva and Eublemma minima, stating that the last two records are
doubtful and the collector and identifier are not given. Finlayson (1967) records
this species from Acrobasis (Phycitidae).
Distribution: This species is widely distributed in Eastern North America.
It ranges northwestwards to British Columbia and Yukon Territory. In these
areas it is partially replaced by a closely related species, D. borealis
Walkley.
1b. DELOMERISTA NOVITA EUROPA, n. subsp.
This subspecies is extremely close to the nominate subspecies from the
Nearctic Region, but the hind tibia and tarsus are black except for whitish
basal rings, in which character it somewhat approaches Delomerista borealis.
The distinguishing characters are: Sensillae on basal two flagellar seg-
ments fewer in number. Propodeum smoother dorsally. Areola elongate,
narrowed basally, almost pentagonal in outline. Nervellus intercepted in lower
0.3-0.45. Hind corner of pronotum yellow. Tegula yellow, with a brownish
spot near wing base. All coxae, trochanters and femora brownish, shiny.
Fore and middle tibiae and tarsi brown. Hind femur only faintly infuscate
apically. Hind tibia and tarsus wholly black except for narrow basal yellowish-
white rings.
Male has the usual characters like face, scape and pedicel ventrally, fore
and middle leg wholly, and hind tibia ventrally, yellowish-white. Hind femur
black only apically. Malar space 0.2-0.25 the basal width of mandible, black.
Nervellus intercepted at lower 0.25-0.3.
This subspecies has been confused with D. mandibularis Gravenhorst,
according to misdeterminations of Roman and others. Specimens reported as
novita by Kasparyan (1977) probably belong to this subspecies. His specimens
were not checked.
Length: 2, 11-13 mm. Fore wing 9-11 mm. Ovipositor 6-7 mm. © 9-11
mm. Fore wing 6-8 mm.
Holotype: ¢, Germany: Bayr. Wald Waldmunchen, 800 m, VII-1948,
14 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
G. Heinrich (labelled D. mandibularis) (TOWNES).
Pavatypes (2%, 99): Germany: Hahnheide b. Trittau, near Hamburg, 1%,
VIl-1945, G. Heinrich (Townes). Furstenberg i.M., Fr. W. Konow, 4%,
Baker Collection (one det. as 7andibularis) (Washington). Austria: Osterich-
Tal. Allgau, 1100 m, 19, 31-VII-1949, G. Heinrich (det. mandibulavis)
(Townes) Poland: 12, ex Diprion similis (abnormal, propodeum and abdomen
banded with red) (Washington). Sweden: Skane, Trap 2, 12, VII-1969, B.
Svensson (Townes).Messaure, 1°, 27-VI-1971, K. Muller; Loderupstrandbad,
1°, 9-VI-1961, M. Townes & C. West (Townes). England: Oxford, Bagley '
Woods @, 25-IX-1960, H. K. Townes (Townes).
Host: Diprion similis.
Distribution: Germany, Austria, Poland, Sweden, — and probably
U.S. 5. RR.
2. DELOMERISTA BOREALIS Walkley (figs. 7-9)
Delomerista borealis Walkley, 1960. In Townes and Townes: Bull.
U.S. Natl: Mas:; 216(2)+ 370.° 28 Type. 2; “NWT: ‘Long 141% w,
Lat 69° 20'N (Border of Alaska and Yukon Territory) (Washington).
Examined in 1980. Paratypes from Alaska, Yukon Territory, North-
western Territory, Quebec, and Colorado.
Taxonomy: Kasparyan, 1977: 71.
This species is extremely similar to D. novita and could well be considered
as a subspecies of the latter, but for distributional overlaps and a few structural
differences, as follows:
Female: First flagellar segment with fewer rows of sensillae. Face
smoother and with sparser punctures. Inner margin of eye only slightly
indented opposite antennal socket. Frons more deeply excavated. Malar
space 0.4 to 0.45 the basal width of mandible. Nervellus intercepted at its
lower 0.4 to 0.45. Propodeum subpolished. Areola more rounded basally
and elongate than in novita. Abdomen granulose. Ovipositor longer, about
0.75 to 0.8 as long as the body, and often longer than the abdomen.
Black. Malar space and mandible white. Hind corner of pronotum black,
or white at its junction with tegula. Tegula black. Legs more uniformly .
reddish-brown with fore coxa and trochanters often blackish-brown. Middle
tibia and tarsus fuscous. Hind tibia and tarsus black, the tibia often with a
small white spot dorsally near base. Apex of hind femur sometimes blackish.
Male: Face and clypeus white, with clypeus black margined. Malar space
yellow, 0.3 the basal width of mandible. Tegula black. Scape and pedicel
black. Flagellum blackish. Hind tibia often yellow underneath. Hind femur
black on apical 0.2, this black mark rather sharply contrasting with the
reddish-brown color of femur.
Length: °, 7-13 mm. Fore wing 5.5-9 mm. Ovipositor 6-9 mm. ©, 7-11
mm. Fore wing 5-8 mm.
Specimens examined: 12% and 40 from the Nearctic Region, from the
following localities: Alaska (Anchorage, Deering, Isabella Pass, Mt. McKinley,
Valdez); British Columbia (Racing River, Stone Mt. Park); Colorado (Poudre
Lake, Fall River Pass in Rocky Mt. Nat. Park and Gould); Northwest Terri-
tories (North Shore of Lac Mounoir, Mackenzie Riber Delta, Norman
Wells, and Tuktoyaktuk); and Yukon Territory (Dawson, Dempster Highway,
mile 51, Herschel Island).
V. Gupta: Genus Delomerista (Ichneumonidae) 15
Walkley (1960) also reported this species from Quebec, Canada. Kasparyan
(1977) reported it from European USSR. These specimens have not been seen.
Three paratypes of this species from Rampart House (YT), Raindeer Depot,
Mackenzie Delta, (NWT), are now assigned to another species, D, walkleyae,
n. Sp.
Host: Unknown.
Distribution: Northwestern parts of North America and also in U.S.S.R.
3. DELOMERISTA LEPTECES Walkley (figs. 13, 14,15, 16, 19)
Delomerista lepteces Walkley, 1960. In Townes and Townes: Bull.
U. S. Natl. Mus., 216(2): 368. @. Type: ¢, Alaska: Mt. McKinley,
1600 ft (Washington). Examined in 1980. Paratypes from Quebec and
Colorado.
This species is characterized by having a slender ovipositor with a pointed
and needle-like tip, both valves tapering apically and lower valve with weak
teeth. Other characteristic features of the species are:
Female: First flagellar segment (fig. 15) with one or two rows of sensillae,
about 1.4 the second segment. Face with indistinct punctures, leathery in
appearance. Malar space 0.45-0.5 the basal width of mandible. Propodeum
a little rough and shiny dorsally, sparsely and shallowly punctate laterally.
Areola horse-shoe shaped. Petiolar area rugulose. Costula absent. Second
lateral area somewhat depressed. Nervellus intercepted at its lower 0.33.
Discoidella bent down in the middle (in other species it is straight or only
weakly curved). First tergite granulose, its lateral carina incomplete, partly
erased apicad of spiracle. Ovipositor fine, needle-like, about 0.6 as long as
the body length and only a little shorter than the abdomen (0. 87).
Black. Mandible, malar space and palpi yellowish-white. Clypeus brown.
Hind corner of pronotum elongately yellow. Tegula yellow to brownish. Fore
coxa black. Fore femur and tibia black dorsally and yellow ventrally. Fore
tarsus blackish-brown. Middle and hind coxae reddish-brown. Middle tibia
and femur yellow in front, with their apices and tarsus brownish-black. Hind
femur reddish-brown with apical third of it and hind tibia and tarsus black
except for one or two yellow spots on tibia ventrally.
Male: Face and clypeus white. Face wider. Malar space black, 0.3 the
basal width of mandible. Scape and pedicel black. Flagellum black. Tegula
yellow. Hind femur reddish or reddish-brown with a blackish mark on apical
0.3. Propodeal areola weaker than in the female.
Length: ¢, 8-10.5 mm. Fore wing 7-8 mm. Ovipositor 4-5mm. ¢,
8-9 mm.
Specimens: Alaska: Mt. McKinley, 19 (type) (Washington). British
Columbia: Stone Mt. Park, 3800+ft., 1°, 20-VII-1973, “%, 12-VII-1973, H. &
M. Townes (Townes). Colorado: Poudre Lake, Rocky Mountain National Park,
1100 ft., 12 (paratype), 12-VIII-1948, H. G. & D. Townes (Townes).
Host: Unknown.
Distribution: Alaska, Quebec, British Columbia, and Colorado. Specimen
from Quebec not seen.
4. DELOMERISTA PFANKUCHI (Brauns) (figs. 4, 5, 6, 20)
[Pimpla| (Delomerista) pfankuchi Brauns, 1905. Ztschr. Syst. Hym. Dipt.,
5: 131. 2. des. Type ?, Bremen, Germany (Berlin). Examined in
1980.
16 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Troctocerus unicolor Hedwig, 1959. Nachr. Naturw. Mus. Aschaffenburg,
62: 96. 2. Syn. by Horstmann,1981. South Italy and Turkey.
Taxonomy: Walkley, 1960: 371. Kasparyan, 1977: 74.
The ovipositor of this species is also long tapered but the lower valve is
more tapered apically than the upper valve and has more distinct teeth along its
tapered part. This species is distinctive in having the abdominal tergites
closely irregularly punctate, rather than granulose or coriaceous.
Female: Antenna 32 segmented. Subapical segments a little longer than
wide. First flagellar segment with two rows of two or three sensillae each.
Malar space 0.25 the basal width of mandible. Interocellar distance equal to
ocellocular distance. Face minutely punctate. Mesopleurum and metapleurum
shiny and with scattered minute punctures. Propodeum subpolished, with a few
scattered punctures laterally. Areola elongate, more pentagonal. Propodeal
carina not strong. Costula faintly indicated, rather weak. Abdomen closely
irregularly punctate. Nervellus intercepted in lower 0.35. Ovipositor as
long as abdomen, its tip with a weak node, long tapered apically.
Blackish-brown. Two small marks on face below antennal sockets,
mandible, hind corner of pronotum, tegula, and apical margins of second and
the following tergites, yellow; these bands wider on succeeding tergites.
Malar space yellowish-brown. Legs yellowish-brown. Hind tibia and tarsus
blackish-brown, with small yellow spots at base of tibia, underneath in middle
of tibia, and at base of first and second trochanteral segments.
Male: Face, clypeus, mandible, and malar space, yellow. Face more
convex and punctate. Scape and pedicel yellow ventrally. Second lateral area
of propodeum a little rough. Costula more prominent than infemale. Tegula
yellow. Fore and middle legs pale-yellow. Hind tibia yellowish-white and only
apically black. Hind femur orange colored. Abdomen rugoso-punctate, with
narrow apical brownish bands. ;
Length: 8mm. Fore wing 7.5mm. Ovipositor 5 mm.
Specimens: Germany: Bremen, 1% (type), ex Psyche viciella, ex Coll.
Pfankuch (Berlin). Poland, 1°, ex Diprion similis, 28-VIII-1938 (Washington).
Specimen reported by Walkley not examined.
Distribution and Hosts: According to Oehlke (1966) this species is Holarc-
tic and has been reported as parasitic on diprionid cocoons (Diprion pini) by
Sitowski (1925) and de Fluiter (1932) in Poland and Netherlands, respectively.
Aubert (1969) reported this species from Germany, Poland and Netherlands,
mentioning the following hosts: Chionodes tvagicella (Gelechiidae), and
Diprion pini L. (Diprionidae). Kasparyan (1977) reported it from European
USSR.
A male, reared from Diprion similis in Poland (U.S.N.M.) has punctate
banded abdomen and is placed here. A female with the same data, however,
has granulose abdomen and is more like D, novita europa, although it has
banded abdomen, which is never the case in noviia.
This species does not occur in the Nearctic Region. The specimen reported
by Walkley as from ''W.Va."' must have come from Europe. This specimen
has not been examined.
5. DELOMERISTA KUSUOI Uchida & Momoi (figs. 10, 11, 12,17, 18)
Delomerista kusuoi Uchida & Momoi, 1957. Insecta Matsumurana, 21(1-2):
10. des., fig. Type ¢, Japan: Kyoto (Sapporo). Examined in 1980.
V. Gupta: Genus Delomerista (Ichneumonidae) 12
This species was described from two females from Kyoto. It is related to
D. pfankuchi Brauns in having a punctate abdomen and a tapered ovipositor with
a subapical nodus. It also has the two yellow subantennal marks on face as in
pfankuchi. D. kusuoi, however, is larger and stouter with body black rather
than brownish, with narrowly red apical bands on abdominal tergites, and pro-
podeum densely punctate and strongly carinate. Other important diagnostic
characters are: 3
Female: Antenna longer, 41-segmented, subapical segments short, and
thick, as long as wide (cf. pfankuchi). Basal flagellar segments with numerous
sensillae. Interocellar distance about 1.3 the ocellocular distance. Face
punctate. Middle lobe of mesoscutum a little elongate anteriorly. Propodeum
densely punctate. Second lateral area rugose. Areola apically tending to be
rugose. Areola well defined, rounded basally and broadly horse-shoe shaped.
Costula distinct and complete, though low as compared to other carinae.
Apical transverse carina bounding the petiolar area very strong. Abdomen
punctate, more strongly so than in pfankuchi.
Black. Antenna ventrally, two triangular spots below antennal sockets,
base of mandible, malar space, tegula, and fore and middle legs, yellowish-
brown. Antenna a little darker. Hind coxa and femur reddish-brown, its
trochanters yellowish-brown, its tibia black dorsally and apically and yellowish
ventrally, its tarsus blackish-brown with base of first segment yellowish-brown.
Hind femur blackish at extreme apex. Abdomen black with narrow, faintly
reddish apical bands, particularly on second to fifth segments. Intersegmental
membranes, where visible (fifth segment onwards), yellow.
Male: Unknown.
Length: 2, 13mm. Fore wing 10.5 mm. Ovipositor 6 mm.
Specimen: Japan: Kyoto (Honshu), 12 (type), 29-X-1955, Kusuo Iwata
(Sapporo).
In the original description the month of collection mentioned is May. There
was also a paratype with the same data, which has not been seen.
Host: Unknown.
Distribution: Japan.
Tl. THE FRIGIDA GROUP
First flagellar segment without sensillae or only one or two present.
Second segment with few sensillae. Malar space 0.4 to 0.5 the basal width of
mandible. Notauli deeper than in Novita Group. Propodeum rough. Petiolar
area rugulose. Areola as long as wide, sometimes longer. Second lateral
area depressed and differently sculptured. Costula indicated by a wrinkled
line. Propodeum with a dorsal flat face, not evenly sloping to apex. Oblique
grooves on second tergite shallower than in Novita Group. Ovipositor tip not
compressed, a little bulbous. Upper valve not nodiform, slightly thicker than
the lower valve and with one or two indentations or ripple-like formations
preapically whence it evenly tapers apically. Lower margin of upper valve
slightly convex to almost straight (in Novita Group concave and less in depth
than lower valve). Ovipositor as long as abdomen or a Little longer.
The American species of this group are similar to and sympatric with the
species of the Novita Group, and have been mixed up with them in the past.
Besides the ovipositor tip, other useful characters are the yellow ventral
aspects of fore femur and tibia and the absence or near absence of sensillae on
the first flagellar segment, and the second segment also with no or fewer sen-
sillae. The European species frigida Kasparyan has wholly reddish fore legs
18 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
and is closely related to the American species, townesorum and walkleyae,
described below as new species.
6. DELOMERISTA FRIGIDA Kasparyan
Delomerista frigida._Kasparyan, 1977. New and Little-known Insects of
European U.S.S.R. Acad. Sci. USSR, 1977: 71. ¢%. key, des., fig.
Type: ¢, Russia (Leningrad). Paratype examined, 1980.
Female:. Face somewhat granuloso-punctate medially. Malar space 0.5
the basal width of mandible. Eye only slightly indented opposite antennal soc-
ket. Thorax as usual, with mesoscutum somewhat hairy and pleural areas
smooth. Metapleurum with minute punctures. Propodeum rugulose in pleural
area, second lateral area and petiolar area; smooth basodorsally. Areola
elongate horse-shoe shaped. Costula represented by depressions and a wavy
line. Abdomen granulose. First tergite more convex and granulose laterally,
its median and lateral carinae somewhat indistinct and confined around its
basal declivity. Ovipositor straight, its tip a little bulbous and evenly sloping.
Ovipositor about 0.75 the length of body and a little longer than the abdomen.
Black. Malar space and mandible yellow. Clypeus blackish-brown. Tegula
black. Hind coxa blackish-brown. Legs reddish-brown. Middle tibia and tar-
sus fuscous. Hind femur and tarsus black. Hind tibia dirty white sub-basally.
Male: Unknown.
Length: 2, 7mm. Fore wing 6mm. Ovipositor 5 mm.
Specimens: Russia: 19, (paratype) (Townes). Germany: Haag Amper,
Ober Bayern, 1%, May 1948 (det. as D. laevis) (Washington).
Host: Unknown.
Distribution: Palaearctic Region: U.S.S.R. and Germany.
7. DELOMERISTA WALKLEYAE, n. sp. (figs. 21, 22, 23, 24, 25)
Female: Face subpolished, with distinct minute scattered punctures.
Malar space about 0.45 to 0.5 the basal width of mandible. Eye moderately
indented opposite antennal socket. Thorax as usual for the genus, but meso-
pleurum with scattered minute punctures, which are less evident in smaller
specimens. Propodeum rugulose in pleural area, petiolar area, and in second
lateral area (as in frigida) and smoother basodorsally. Areola horse-shoe
shaped. Costula faintly indicated (fig. 21). Lateral aspect of postpetiole flat
to a little concave, more rugulose rather than granulose. Lateral carina more
prominent than in frigida. Abdominal tergites finely granulose. Oblique
grooves on second tergite weaker. Ovipositor long, about 0.7 as long as body
and longer than abdomen, a little arched in larger specimens.
Black. Malar space and mandible yellowish-white. Clypeus brown. Hind
corner of pronotum black to narrowly yellow. Tegula black. Fore leg largely
blackish (type) with femur and tibia yellow ventrally. Mandible and hind coxae,
trochanters, and femora reddish-brown, and their tibiae and tarsi black.
Middle tibia yellow ventrally. Hind tibia dirty yellow to brownish yellow baso-
ventrally (more often brownish rather than yellow). Hind femur with a narrow
apical fuscous dorsal mark. Abdomen black.
Male: Unknown.
Length: ¢, 8-10 mm. Fore wing 6-7 mm. Ovipositor 5-6 mm.
Holotype °, Alaska: Tsaina River, 17.VUI.1973, H. & M. Townes
(Townes).
V. Gupta: Genus Delomerista (Ichneumonidae) 19
Paratypes: 16°. Alaska: Anchorage, ?, 6 to 12-VII-1976, Peter A. Rush.
Thomson Pass, 2, 15-VIII-1973, H. & M. Townes (Townes). King Salmon,
Naknek River, 12, 19-VII-1952, J. B. Hartley (Ottawa). Northwest Terri-
tories: Mackenzie River Delta, 68° 43°N, 1349 15° W, 22, 18 to 19-VII-1979,
L. Humble (det. D. borealis) (Ottawa). Mackenzie Delta, Raindeer Depot,
12, 10-VII-1948, J. P. Vockeroth (paratype of D. borealis Walkley) (Ottawa).
North Shore of Lac Maunoir, 22, 15-VII-1969, G. E. Shewell (Ottawa).
Kovaluk R., 69° 11°N, 1319 W, 29, 19 to 24-VI-1971, W. R. M. Mason
(Ottawa). Norman Wells, 2, 27-VI-1969, G. E. Shewell (Ottawa). Yukon
Territory: Rampart House, ¢, 20-VII-1951 and 2, 11-VII-1951 (paratypes of
D. borealis Walkley), J. E. H. Martin (Ottawa). Dempster Highway, mile 51,
°, 7 to 12-VII-1973, G. & D. M. Wood (Ottawa). British Columbia: Stone Mt.
Park, 3800+ft., 2°, 12 and 19-VII-1973, H. & M. Townes (Townes).
Host: Unknown.
Distribution: Northwestern Nearctic Region. Sympatric with D. borealis,
8. DELOMERISTA TOWNESORUM, n. sp. (figs. 26, 27, 28)
Female: Face subpolished, somewhat leathery,without distinct punctures
or laterally with a few scattered punctures. Malar space 0.3 to 0.4 the basal
width of mandible. Eye shallowly indented opposite antennal socket. Meso-
pleurum polished, with only minute setiferous punctures. Propodeum sub-
polished to a little wrinkled laterally. Areola as is walkleyae, but costula
faint and second lateral area smoother. Nervellus intercepted in upper 0.4.
Abdomen including postpetiole granuloso-mat. Ovipositor straight or a little
upcurved, about as long as the abdomen, and 0.55 to 0.6 as long as the body.
Black. Malar space and mandible yellow. Clypeus brownish-black (some-
times face also like clypeus). Hind corner of pronotum and tegula yellow. All
legs pale yellowish-brown with fore tibia dorsally fuscous and ventrally yellow-
ish. Middle and hind tibiae yellow with dorsal and apical blackish marks.
Middle and hind tarsi black with base of basitarsus yellow.
Male: Face and clypeus yellowish-white. Malar space 0.25 to 0.3 the
basal width of mandible, yellow. Scape andpedicel yellow ventrally, scape
often only narrowly so. Tegula yellow. Nervellus intercepted almost at its
center or inupper 0.45. Fore and middle coxae yellowish-white. Hind femur
reddish-brown with only its apex black marked.
Length: 2,7-10 mm. Fore wing 6-8 mm. Ovipositor 5-6 mm. ©, 7-10
mm. Fore wing 6-8 mm.
Holotype: °, Michigan: Midland County, 21-31-V-1961, R. R. Dreisbach
(Townes).
Paratypes (250°, 229): Michigan: Ann Arbor, 42, 15 to 17-V-1960, 28-V-
1962, 30-V-62, 7-VI-1962, H. & M. Townes (Townes). Schoolcraft Co., %,
8-VI-1960, R. R. Dreisbach. Emmet Co., 5°, “, 27-V-1960, R. R. Dreis-
bach. Charlevois Co., %, 31-V-1960, R. R. Dreisbach (all Townes). Oregon:
Mt. Hood, 5400, %, 24-VII-1978, 20, 20-VII-1978, 19, 26 to 28-VII-78, H. &
M. Townes (Townes). Washington: Mt. Rainier, 2700 ft., 20°, 3°, 11-VII to
16-VIII-1940, H. & M. Townes (Townes). Avizona: Nr. Alpine, 50, 24 to 29-
V-1947, H. & M. Townes (Townes). British Columbia: Robson, ?, 10-VI-1945,
H. R. Foxlee (Townes), ¢, 24-V-1950, H. R. Foxlee (Ottawa). Stone Mt. Park,
3800+ ft., 14%, 12 to 22-VII-1978, H. & M. Townes (Townes). Saskatchewan:
Regina, $, 14-VI-1940, T. B. Rempel (Townes). Saskatoon, 8, 22-VI-1923,
N. J. Atkinson (labelled D. novita) (Ottawa). Ontario: Golden Lake, 2, 9-VI-
1952, G. S. Walley (Ottawa). Jowa: 2, 11-VI-1938, B. Berger (det. D. novita)
20 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
(Washington). Virginia: ?Blacksburg, 19 (labelled D. novita) (Washington).
Host: Unknown.
Distribution: This species is sympatric with D. novita and has been con-
fused with the same in the past. Apparently a widespread species in North
America, as is D. novila.
A large female from Washington: Mt.Rainier, approaches D, walkleyae
in facial punctures, pleural punctures, but otherwise agrees with townesorum.
Similarly a male from Emmet Co., Michigan, has black scape and pedicel,
but otherwise resemble the males of ftownesorum.
C. THE JAPONICA GROUP
Basal flagellar segments with sensillae. Propodeum short and slanting,
with a short dorsal face (figs. 29, 34,41). In profile view evenly sloping from
base to apex (fig. 40). Areola broadly triangular, or semicircularly arched.
Region of costula linearly depressed and wrinkled, with an appearance of a
carina, though costula often faint to indistinct. Apical transverse carina
strongly arched and petiolar area occupying the apical half of propodeum.
Petiolar area subpolished and with a few rugosities. First tergite widened
basally, almost parallel-sided, or a little flanged at the junction of dorsal
and lateral carinae towards base; this segment comparatively thinner and more
compressed than in species of groups A and B. Median dorsal carinae not very
distinct on postpetiole. Upper valve of ovipositor tip a little bulbous and
widened, its apical slope abrupt, the sloping portion demarcated by two little
humps on the dorsal valve, and about as long as the width of ovipositor at this
point (which is the maximum width of the ovipositor). Ovipositor tip demar-
cated from the rest of ovipositor by a weak constriction, which appears char-
acteristic of the group. Line of junction of upper and lower valves straight.
Upper and lower valves of equal depth. Apical ridges on lower valve reclining,
while the basal ones inclining. Ovipositor about 0.79 the length of abdomen.
This group includes three closely related species: D. japonica Cushman
from Japan and USSR, D. diprionis Cushman from North America, and
D, indica, n. sp. from the Himalayan mountains of India. The former two
species have often been synonymized or considered subspecies of each other.
A key to these species is not very satisfactory because of certain overlapping
characters. Reference should therefore be made to the diagrams and descrip-
tions of the ovipositor tips (figs. 33,38,39 and 44), to the shape of the propo-
deum (figs. 29, 34,40 and 41), and also to the nature of the first tergite, malar
space and nervellus, to separate the species.
9. DELOMERISTA DIPRIONIS Cushman (figs. 34-38)
Delomerista diprionis Cushman, 1939. J. Washington Acad. Sci., 29: 398.
Oo, 2. Type 2, Canada: Oakville, Ontario (Washington). Examined in
1980. Hosts: Diprion spp., Neodriprion spp.
Delomerista japonica Cushman: Walkley, 1960. Jn Townes and Townes:
Bull. U. S. Natl. Mus., 216(2): 367. Syn. in part.
Delomerista japonica diprionis Cushman: Carlson, 1979. In Krombein
et al. : Catalog of Hymenoptera north of Mexico, 1: 349.
Biology: Furniss & Dowden, 1941: 49-51. Griffiths, 1960: 656. Torger-
sen, 1969: 60.
Morphology: Finlayson, 1960: 25 (larva). Short, 1978: 25, 174 (larva).
V. Gupta: Genus Delomerista (Ichneumonidae) 21
This species was synonymized with D. japonica Cushman by Walkley
(1960). The types have been examined as well as other material of the two
taxa. In my opinion, the two species are related but distinct. Although
diprionis shows a great degree of variability, it can be separated from japonica
by the combination of characters mentioned above.
This species has been reared in North America on a number of hosts,
belonging to the genera Diprion, Gilpina and Neodiprion. The variations could
not be correlated either with the host associations or with the distribution of
the species, and therefore D. diprionis is considered to be a polymorphic and
widely distributed species in the Nearctic Region. The larval head (fig. 64) is
somewhat different from that of japonica (fig. 65).
Female: Head wider than long. Face a little convex and punctate. In
smaller-sized specimens face with a few longitudinal striations medially.
Orbital areas smooth. Clypeus smooth. Malar space 0.6 to 0.7 the basal
width of mandible. Frons and vertex smooth. Mesoscutum evenly convex,
with minute setiferous punctures. Scutellum also with minute setiferous punc-
tures. Pronotum smooth. Mesopleurum with a few minute and scattered punc-
tures but more shiny than mesoscutum. Metapleurum shiny but with minute and
denser punctures, more so than on mesopleurum or mesoscutum. (In speci-
mens from Alaska and British Columbia, the metapleurum is variable from
smooth to a little rugulose). Propodeum variable. Areola varying from tri-
angular to wider and more semicircularly arched or crescentic in outline.
Costula faint to distinct (even paratypes from same host and locality vary).
Propodeum smooth baso-dorsally, somewhat punctate laterally, and petiolar
area usually rugulose or with a few rugosities. Second lateral area often
depressed and punctate. Propodeum in profile appearing short and abruptly
sloping, with dorsal face short, less than half the length of propodeum, and
apical slope nearly vertical. Nervellus intercepted at lower 0.3. First tergite
rather stocky and thicker medially, with its dorsomedian carinae making an
angle of 45° with the horizontal axis. Its lateral carina either interrupted in
the region of spiracle, or faded out apically. Area between lateral carina and
ventral carinae wider and rough, tending to be rugose. Juction of lateral and
median carinae not conspicuously flanged out. Basal declivity of first tergite
dull. Central raised area of postpetiole granulose and laterally rugulose. All
abdominal tergites coarsely granulose. Ovipositor tip (fig. 38) thicker and with
a convex even apical slope. Upper valve a little widened preapically. In pro-
file view ovipositor appears more parallel-sided and without a preapical con-
striction as seen in japonica (fig. 39).
Black. Mandible, malar space, hind corner of pronotum and tegula,
yellowish-white. Clypeus brown to black. Legs reddish-brown to yellowish-
brown, with hind femur just apically, hind tibia except for an elongate white
baso-ventral mark and hind tarsus (except for a white basal mark), black.
Fore coxae sometimes brownish. Fore and middle tibia whitish ventrally and
faintly blackish dorsally, though often more uniformly brownish. Hind tibia
_ sometimes largely black but always with a yellowish-white basal annulus.
Color of tegula variable from yellow to black.
Male: Face and propodeum a little more dull rugulose. Scape and pedicel
yellow. Face yellowish white. Malar space yellow and about 0.3 the basal
width of mandible. Fore and middle legs yellow with dorsal fuscous marks on
femur, tibia and tarsus. Hind trochanters yellow. Hind femur reddish-brown.
Rest of coloration and sculpture as in female. Tegula usually yellow.
Variations: The majority of specimens reared from Diprion, as well as
from Neodiprion, show pale yellow tegula and hind tibia white or pale yellow on
22 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
the underside, rather than this color confined to base. Usually specimens
reared from Neodiprion are smaller than those reared from Diprion. Speci-
mens from Quebec generally have hind tibia brownish-black except at base.
Specimens from British Columbia, Northwest Territory and Yukon Terri-
tory show a tendency of having brownish-black tegula and specimens from
Alaska, as well as from British Columbia mountains have a wholly black tegula.
Usually all coxae are reddish-brown, but often specimens from Alaska as well
as from British Columbia show black or blackish fore coxae and hind tibia and
tarsus wholly black or only their bases white.
In smaller-sized specimens reared from Neodiprion in Ontario, the costula
is absent and propodeum is more shiny, with only a faint depression in the
second lateral area. In larger sized specimens from Ontario, reared from
Diprion similis, the costula is marked by a distinct crease with second lateral
area depressed and punctate.
Length: 2, 4.5-10 mm. Fore wing 4-7 mm. Ovipositor 3-4mm. ¢,
4-8mm. Fore wing 3.5-6 mm.
Specimens: Several males and females from the Nearctic Region as follows:
Alaska (Anchorage, Richardson Highway,at Mi 249, Taku Harbor, Union Bay);
Alberta (Miette Valley, Jasper Park); British Columbia (Awun River, Allard
Lake, Clinton, Cottonwood, Goderich, Lac la Hache, Maynard Lake, Revel-
stoke, Sayward, Victoria, Robson); California (Fish Camp, Sherwood, Straw-
berry); Connecticut (New Haven); Idaho (Fairfield); Manitoba (Aweme, Sand
Hills); New Brunswick (Fredricton); New Hampshire (Mt. Madison); New
Jersey (Moorestown); New York (Watson); North Carolina (Clingmans Dome,
Mt. Mitchell); Northwest Territories (North Shore of Lac Maunoir, Norman
Wells, McConnell, Kovaluk River, Raindeer Depot, Tuktoyaktuk); Nova Scotia
(Liscombe River, Lum Co.); Ontario (Biscotasing, Cobden, Constance Bay,
Grand Bend, Hawk Lake, Merivale, Oakville, Renfrew, Southampton, Sydney);
Quebec (Church Cr., Cumshewa Inlet, Brome, Great Whale River, Georgeville,
Knob Lake, Laniel, Montreal, Norway Bay); Washington (Mt. Rainier, 4700 ft.,
Snoqualmie Pass); Wisconsin (Gibson Lake, Gordon, Polk Co.); Yukon Tervi-
tory (Dempster Highway at mile 37, Herschel Island, White Horse).
Specimens reported by Walkley from Maine, Michigan, Minnesota, Oregon,
and Vermont were not seen by me.
Hosts: Diprion similis, Diprion polytomum, Gilpina frutetorum, G. her-
cyniae, Neodiprion lecontei, N. nanulus nanulus, N. pratti banksianae,
N. sertifer, N. tsugae, N. abietes.
The larval head is figured in fig. 64.
Distribution: Widespread in northern North America.
10. DELOMERISTA JAPONICA Cushman (figs. 29-33, 39)
Delomerista japonica Cushman, 1937, Insecta Matsumurana, 12: 35.
o, &. des. Type °, Japan: Nagawa-Mura, Nagano-ken (Washington).
Examined in 1980. Host: Diprion nipponicus.
Taxonomy: Walkley, 1960: 367 (in part). Kasparyan, 1977: 73 (in part).
Morphology: Short, 1978: 25,175 (larva).
This species is extremely similar to D. diprionis and the two were con-
sidered synonymous by Walkley, and as subspecies by Carlson (1979). The
nature of the ovipositor tip (figs. 38,39) is different in the two: in japonica
the tip is with an abrupt apical slope and with a preapical constriction. The
differences in the two subspecies are rather subtle, but the combination of
V. Gupta: Genus Delomerista (Ichneumonidae) 23
characters mentioned in above should distinguish the two, as well as the
related D, indica. Larval head as in figure 65.
Male and Female: Malar space 0.33 to 0.45 the basal width of mandible.
Face a little more strongly arched and punctate than diprionis specimens of
the same size. Mesoscutum somewhat subpolished, leathery. Mesopleurum
and metapleurum smoother and more polished. Propodeal areola more hex-
agonal in outline. In profile view, propodeum rather evenly convex and with a
convex Slope. Dorsal face of propodeum about half the length of propodeum,
apical slope more inclined rather than vertical. First tergite thinner in depth,
with dorsomedian carinae making an angle of 30° with the horizontal axis.
Lateral carina complete to apex and area between it and ventral carina narrow
and granulose to rugose. Junction of lateral and median carinae conspicuously
flanged out. Basal declivity of first tergite smoother and shiny. Central
raised area of postpetiole flat and rugulose. Abdomen more rugulose rather
than granulose, more often ruguloso-granulose. Ovipositor tip small, tapered,
in profile view a little widened preapically (fig. 33), somewhat bulbous and then
abruptly sloping to a point. Upper valve with a straight and short slope.
Color essentially similar to that of D. diprionis. Fore leg usually
yellowish-brown and a little lighter in color than middle and hind legs. Hind
femur with only a faint infuscate apical mark. Sometimes tegula and apex of
hind femur brownish.
Length: ¢, 8-9mm. Fore wing 6.5-7 mm. Ovipositor 3.5-4 mm.
o, 8-9 mm. Fore wing 6.5-7 mm.
Specimens: Japan: Nagawa-Mura, Nagano-ken, 2 (type) Jan. -March 1937
(Washington). Same locality, $, °, (Washington). Kamikochi,Japan, “, 38,
July 22 to 23, 1954, Townes family (Townes).
Host: Diprion nipponicus.
Distribution: Eastern Palaearctic Region: Japan. Kasparyan (1977)
reported it also from USSR.
11. DELOMERISTA INDICA, n. sp. (figs. 40-46)
Male and Female: Face a little protuberant medially, punctate. Clypeus
flat, subpolished. Malar space 0.5 the basal width of mandible. Frons, ver-
tex, occiput and temple subpolished, shiny, with vertex posteriorly and temple
sparsely hairy. Interocellar distance equal to the ocellocular distance. Meso-
scutum and scutellum mat, evenly convex, with minute setiferous punctures.
Side of thorax shiny. Metapleurum with a few distinct scattered punctures
and area near hind coxa rugose. Propodeum subpolished, with irregular punc-
tures laterally on pleural areas and scattered rugosities on lateral area and
petiolar area. Areola more squarish or triangular, with lateral carinae semi-
circularly arched. Costula interrupted, represented by a linear wrinkled line.
Propodeum depressed in this area. Nervellus intercepted at the middle, with
some specimens showing variations: intercepted a little above or below the
middle. Abdomen finely granulose to granuloso-coriaceous; apical margins
and terminal tergites mat. First tergite evenly arched (fig. 42), depressed
medially, its dorsomedian carinae not very distinct and bordering a shallow
basal declivity, which is dull and granuloso-mat. Lateral carina just above
spiracle complete, moderately flanged out basally, and area below it rugulose.
Central depression on postpetiole granulose, bordered by rugosities (granuloso-
rugose). Ovipositor tip evenly tapering and not very bulbous (fig. 44), the
upper valve a little heavier near tip and with an even convex slope, as in
D, diprionis.
Female color: Black. Malar space, mandible except teeth, hind corner
24 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
of pronotum, tegula (except for a black apical spot), and wing bases, yellow.
Legs reddish-brown with trochanters and stripes on anteroventral aspects of
fore and middle femora and ventral region of basal 0.75 of hind tibia, yellow.
Apex of hind femur, hind tibia otherwise, and hind tarsus black. Apical tarsal
seement of fore and middle legs darker.
Male color: Face, clypeus, mandible except teeth, yellow. Scape and
pedicel yellow ventrally. Hind corner of pronotum and tegula yellow. Fore
and middle coxae and their trochanters yellow, their tibiae and femora marked
with brownish, apical tarsal segments darker. Hind coxa and femur reddish-
brown, hind trochanters yellow, hind tibia and tarsi black with tibia ventrally
(except at apex) and base of first tarsal segment, yellow.
Length: 2, 8.5to9.5 mm. Fore wing 7.5-8 mm. Ovipositor 3.5-4 mm,
o, 8-9 mm. Fore wing 7-8 mm. |
Holotype:2, India: Himachal Pradesh: Dhenkund (near Dalhousie), 2743 m,
25-IX-1971, Coll. Gulati. (Gupta).
Allotype:%, same data, Coll. Tulsi, DJD-168 (Gupta).
Pavatypes: Several %, ¢. India: Himachal Pradesh (Dalhousie, 2132 m,
Dhenkund 2743 m, Ahla 2286 m, Kalatop 2488 m, Khajiar,1828 m,all localities
in Dalhousie Hills, collected from May to October 1971 and July 1965.)
(Gupta).
Host: Unknown.
Distribution: India: Mountains of Himachal Pradesh.
D. THE MANDIBULARIS GROUP
Basal flagellar segments with fewer to several sensillae (fig. 55-62).
Malar space 0.4 to 0.6 the basal width of mandible (except in laevis, where it
is 1.0 to 1.2). In males malar space 0. 33 to 0.4 the basal width of mandible
(in laevis 0.8). Propodeum convex; in profile view (fig. 50,54) with basal
part convex and apical part abruptly sloping, almost vertically so. Costula
faint to indistinct. Propodeum generally granulose to rugulose in pleural
area, second lateral area and petiolar area. Often petiolar area with a few
wrinkles. First tergite convex, with lateral carina distinct and usually com-
plete. Median carinae usually distinct to the dorsal hump and then weak. Ovi-
positor stout. Upper valve heavy (figs. 47-49, 51-53) and occupying the greater
part of the depth of ovipositor, except in D. longicauda, where the tip is nar-
rowed preapically and ovipositor is twice as long as the abdomen. Ridges on
lower valve vertical to a little inclined. Basal three ridges strongly inclined.
Upper and lower valves of ovipositor meeting in an arched line and ina slant.
Ovipositor 0.8 to 1.0 as long as abdomen (2.0 in longicauda), usually slightly
arched upwards or bent downwards.
This group includes five species: Delomerista longicauda (with ovipositor
2.0 the length of abdomen), D, laevis (malar space long, 0.8 to 1.2 the man-
dible width), D. stvandi (ovipositor very stout and straight), D. mandibularis
(= gelida, ovipositor slightly curved upwards), and D. masoni (ovipositor bent
downwards and costula strong).
12. DELOMERISTA MANDIBULARIS (Gravenhorst) (figs. 48, 49, 50, 59, 60)
Pimpla mandibularis Gravenhorst, 1829. Ichneumonologia europaea,
3: 180. %. Lectotype (labelled by Perkins, 1936, designated by
Oehlke, 1967). ¢, Poland: Breslau (Wroclaw). Specimens det.
Perkins and Kasparyan examined, 1980.
V. Gupta: Genus Delomerista (Ichneumonidae) 25
Ephialtes albicinctus Desvignes, 1862. Trans. Ent. Soc. London, 1: 226.
Oo. des. Type°%, ?Great Britain (London). Name preoccupied. Syn.
after Fitton (1978). Examined, 1981.
Ephialtes desvignesit Marshall, 1870. Ichneumonidum Britannicorum
Catalogus, p. 20. New name for Ephialtes albicinctus Desvignes.
Delomerista gelida Walkley, 1960. In Townes and Townes: U. S. Natl.
Mus., Bull. 216(2): 366. 2. des. fig. Type °, N.W.T.: Cameron Bay,
Great Bear Lake (Washington). Examined, 1980. New synonym.
Paratypes from Sask: Waskesiu, Quebec: Great Whale River.
Taxonomy: Oehlke, 1967: 34. Aubert, 1969: 99. Fitton, 1976: 326. Fitton,
1978: 14. Kasparyan, 1977: 74.
The Lectotype locality mentioned by Oehlke (1967), who designated the
lectotype, is Breslau (=Wroclaw), while Kasparyan mentions Warmbrunn as
the Lectotype locality. Gravenhorst had specimens from both the localities.
The type of Ephialtes albicinctus Desv. has a label by Perkins (1933) mention-
ing its synonymy with D. mandibularis Grav. This synonymy was never
published by him. Fitton (1978) first published this synonymy.
Female: Firstand second flagellar segments with few sensillae (fig. 59, 60).
Face convex medially and with scattered punctures ona shiny surface. Sometimes
puncturesa littledenser. Clypeus smooth andflat. Malar space 0. 5 the basal width
of mandible. Mesoscutum subpolished with setiferous punctures. Side of thorax
polished and with minute scattered setiferous punctures. Propodeum smooth dorsal-
ly and rugulose laterally and inthe petiolar area. Second lateral area depressed and
rough. Areola smooth, horse-shoe shaped, sometimes a Little squarish or pentagon-
al. Costula faintly indicated byabrokencarina. Seeninprofile, propodeum witha
convex slope (fig. 50). Nervellus intercepted below the middle. Abdomen including
median area of postpetiole granulose. Firsttergiteas infig. 50, with dorsal and lat-
eral carinae distinct and ruguloso-coriaceous on side. Ovipositor stout, of uniform
width, and preapically slightly curved upwards, aslongasabdomen. Ovipositor tip
a little widened (fig. 48, 49), with dorsal valve occupying nearly 2/3 of the depth of ovi-
positor near apex, while the lowervalve a occupying 2/3 of the depth of ovipositor
near base (the two valves meeting ina slant).
Black. Malar space, mandible, andhind corner of pronotum, yellowish-white.
Tegula black, though often narrowly to partly yellowish-white. Legs dark reddish-
brown to orange-brown, with fore leg partly to largely brownish in American popula-
tions. Hindtibiaandtarsus black. Apex ofhindfemur oftenblack. Middle tibia and
tarsus reddish-brownto blackish-brown. Fore coxa brownish-black in Swedish spe-
cimens also.
Male: Face yellowish-white, smoother or a little rugulose in larger speci-
mens. Malar space yellow, 0.3 to 0.4 the basal width of mandible. Scape and
pedicel yellow ventrally, or black. Propodeal carinae strong. Costula faint
to obsolete. Areola elongate. Tegula yellow. Fore and middle legs largely
pale yellow, with their femora and tibiae and tarsi brownish dorsally. Hind
coxa, trochanter and femur reddish-brown. Trochanters often yellow ventrally.
Hind femur sometimes apically black marked. Hind tibia and tarsus blackish-
brown dorsally, with tibia ventrally largely yellowish-white in the middle.
Postpetiole rugose. Abdominal tergites granuloso-mat.
Length: ¢, 8.5to9.5mm. Fore wing 7-8 mm. Ovipositor 6.5-7.5 mm.
Oo, 6-9 mm. Fore wing 5-8 mm.
Specimens examined: 1°, ?England, type of E. albicinctus (London).
England: Newton Abbot, °, 8-VI-1941, as mandibularis by Perkins), J. F.
Perkins (Washington). Russia, “, ?, from Betula, 18-V-1890 (det. as mandi-
bularis by Kasparyan) (Townes). Germany: Siegmundung, , 7-VI-1919 (det.
26 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
as mandibularis by Habermehl) (Ottawa). Northwest Territories: Cameron
Bay, Great Bear Lake, ¢ (type of D. gelida Walkley), 1-VII-1957, T. N.
Freeman (Washington). Quebec: Great Whale River, ¢, 20-VII-1949 (para-
type of D. gelida) (Ottawa).Saskatchewan: Waskesiu, %, ¢, 20-VI-1938, J. G.
Rempel (2 paratype of gelida) (Townes). In addition 28% and 22° from the fol-
lowing localities: British Columbia (Hixon, Ft. Nelson, Racing River, Stone
Mt. Park); Alaska (Anchorage, Delta Junction, Tsaina River); Quebec (Great
Whale River) ,Saskatchewan(Conquest); Northwest Territories (Normal Well,
Kovaluk River, Tuktoyaktuk), Yukon Territory (Dawson), and Sweden (Messaure,
SkAne).
Only males from the following states: Arizona (near Alpine), Alberta
(Banff), California (Leevining), where they occur sympatrically with D. masoni
or D. townesorum. The males show variations and their identities are not
very clear.
In addition, Walkley also reported this species from Ontario, Colorado,
New York and Pennsylvania. Those specimens were not examined.
Hosts: Euura amerinae and Strongylogaster sp. (Tenthredinidae) in Europe.
Distribution: Holarctic. In the Nearctic Region apparently restricted to
Northern and Northwestern parts.
13. DELOMERISTA STRANDI (Ulbricht) (figs. 47, 54, 57, 58)
Pimpla strandi Ulbricht, 1911. Arch. Naturgsch., 77: 149. §&.
Lectotype (designated by Oehlke, 1967), °, ''Norvegia, E., Coll.
Strand, Rosvana" (Berlin). Examined in 1980.
Delomerista strandi: Oehlke, 1967. Hymenopterorum Catalogus (nova
editio),2: 34. Kasparyan, 1977: 74. Russia.
Female: Face centrally a little rugulose and punctate. Malar space 0.5
to 0.6 the basal width of mandible. Basal flagellar segments with fewer
hairs and with several sensillae (figs. 57,58). Frons, vertex and temple
smoother. Thorax dull, hairy. Mesoscutum with close setiferous punctures,
particularly on the middle lobe. Mesopleurum with scattered punctures,
smoother in smaller-sized specimens. Metapleurum partly to largely rugu-
lose. Pleural area of propodeum rugulose. Second lateral area rugulose and
depressed. Rest of propodeum smoother but with a few wrinkles around
carinae. Areola elongate, somewhat pentagonal in outline. Costula incomplete.
In profile, propodeum as in fig. 54. First tergite strongly convex (fig. 54),
rugulose to rugose laterally, its median carinae weak beyond the dorsal hump.
Its lateral carina strong throughout. Abdomen finely granulose. Ovipositor
stout, straight and compressed, its upper valve very wide (fig. 47), and occu-
pying almost 2/3 the apical depth of ovipositor. Ovipositor narrow basally and
widened apically (1:1.5), the line of junction of the upper and lower valves
running obliquely from base to apex of ovipositor. Teeth on lower valve ver-
tical, with basal 3-4 teeth inclined. Ovipositor about 0.8 as long as abdomen.
Black. Malar space and mandible yellow. Tegula black. Legs reddish-
brown with hind tibia and tarsus black. Fore and middle tarsi brownish-black.
Middle tibia fuscous dorsally (legs in type-specimen from Europe a little
paler). Fore coxa and trochanter brownish in the lectotype and in a few
American specimens). Clypeus brown. Sometimes mandible brown rather than
yellow. Hind tibia varying from pale brown to blackish brown. Wings with a
purple iridescence in specimens from Mackenzie River Delta, which are also
larger and stouter specimens.
Male: Unknown.
V. Gupta: Genus Delomerista (Ichneumonidae) 27
Length:?, 7-11mm. Fore wing 5-8 mm. Ovipositor 4-6 mm.
The Lectotype, which is a smaller-sized specimen, has the face smoother,
dull and not distinctly punctate. Otherwise similar to other specimens.
Specimens: "Norvegia, E. Ros Vania’, Coll. Strand. ? (lectotype)
(Berlin) (A cotype of this species is actually a specimen of D. laevis Graven-
horst). Alaska:. mile 28, Richardson Highway, ¢, (det. D. gelida by Walkley),
27-VII-1951, W.R.M. Mason (Ottawa). British Columbia: Stone Mt. Park,
3800+ft., 2, 13-VII-1973, H. & M. Townes (Townes). Alberta: Jasper, 9,
26-VII-1949, C. P. Alexander (Townes). This specimen has longer (0. 8)
malar space). Northwest Territories: Mackenzie River Delta, 68° 43°N.,
1349 15° W., 32, 18 to 29-VII-1979, L. Humble (Ottawa) (det. as D. borealis
in 1980). Norman Wells, 2, 29-VI-1969, S. E. Shewell (Ottawa). Yukon
Territory: mile 87 on Dempster Highway, ¢, 18 to 28-VII-1971, G. & D. M.
Wood (Ottawa).
Host: Unknown.
Distribution: Holarctic Region. In the Nearctic Region, apparently con-
fined to the Northwestern parts.
14. DELOMERISTA MASONI, n. sp.
This species has apparently been confused with Delomerista gelida =
mandibularis in the past, as some specimens from Alaska and British Colum -
bia, in Canadian National Collection, Ottawa bear determination label of
D, gelida Walkley. It can be readily separated from gelida =mandibularis
by the nature of the ovipositor, tegula, propodeum, etc.
Female: Head wide, punctate. Eye moderately deeply notched. Malar
space 0.4 to 0.5 the basal width of mandible. Basal flagellar segments with
sensillae. Mesoscutum subpolished, with numerous setiferous punctures.
Side of thorax polished and with minute setiferous punctures on mesopleurum
and metapleurum; those on metapleurum a little coarser than on mesopleurum.
Pleural area of propodeum irregularly punctate. Propodeum dorsally smoother
and shiny. Areola semicircularly rounded. Costula strong and distinct. All
propodeal carinae strong. Petiolar area subpolished with weak rugulosities
around carinae. Nervellus intercepted in lower 0.3. First tergite short,
humped dorsally, where median carinae angled and getting weaker. Lateral
carina distinct throughout. Abdomen granulose, with postpetiole laterally
and basomedian area of second tergite rugose. Ovipositor 0.8 the length of
abdomen, widened apically from base, with a weak median bend.
Black. Malar space, mandible, hind corner of pronotum, and tegula
yellowish-white. Antenna and clypeus brownish. Legs reddish-brown, with
hind tibia and tarsus largely black. Hind tibia with a basal and ventral yellow .
mark. Hind tarsus with a basal yellow ring. Fore femur and tibia and middle
tibia yellowish ventrally.
Male: Scape and pedicel ventrally yellowish-white. Flagellum brown.
Face, clypeus, mandible and malar space yellowish-white. Fore and middle
legs and hind trochanters, tegula, and hind corner of pronotum yellowish-
white. Hind coxa and femur yellowish-brown. Apex of hind femur narrowly
black, or hind femur wholly yellowish-brown. Hind tibia and tarsus with black
marks and yellow ventrally. Malar space 0.3 the basal width of mandible.
Nervellus intercepted at lower 0.4 to upper 0.4. Dorsal carina of first tergite
usually strong to apex of tergite. Costula present. Propodeal carinae like
those in female.
Variations: This species is rather close to D. stvandi from the northern
latitudes and some specimens of it approach that species. The chief differences
being its yellow tegula, hind tibia not wholly black, costula of propodeum strong
28 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
and complete and propodeum dorsally smoother. However, there are some
specimens where the costula appears a little weak, but complete, second lateral
area rugulose, hind leg more extensively black, and tegula may have a black
spot. In these specimens, generally, the apex of hind femur is also black or
blackish, which is not the case in strvandi, and usually there is a basal yellow
ring on hind tarsus and tibia. The shape of areola is also variable, being a
little elongate and not semicircular in some specimens.
Length: ¢, 9-11 mm. Fore wing 5.5-8.5 mm. Ovipositor 4 -5.5 mm.
o, 9-10 mm. Fore wing 6-8 mm.
Holotype:?, Michigan: Ann Arbor, 30-V- 1962, H. & M. Townes (Townes).
Paratypes: New York: Ithaca, 12, 3-V-1936, H. K. Townes. Pennsylvania:
Spring Brook, ?, 8-VI-1945, H. & K. Townes. Nebraska: Valentine Refuge,
20°, 29, 7-VI-1972, H. & M. Townes (Townes). Ontario: Chaffeys Locks, ¢
(face narrower), 21-VI-1975, J. Belwood (Townes). Ottawa, %, (det. gelida by
Walkley), 29-V-1941, G. S. Walley. Ovegon: Pinehurst, 2, 2-VII-1978. H. &
M. Townes (Townes). 7% from Ochoco Creek, Hyatt Reservoir, Mt. Hood,
June-July 1978, H. & M. Townes (Townes). Colorado: Gould, 1°, 6-VIII-
1974, H. & M. Townes. Avizona: 15%, near Alpine, Oak Cr. Canyon.
(Townes).
Distribution: Nearctic Region, New York to Rocky Mountains.
15. DELOMERISTA LAEVIS (Gravenhorst) (figs. 52, 61, 62)
Pimpla laevis Gravenhorst, 1829. Ichneumonologia europeaea,3: 180.
2. Type 2, Piemont, Italy (Wroclaw).
Pimpla texana Cresson, 1870, Trans. Amer. Ent. Soc., 3: 145. &.
Type ¢, Texas (Philadelphia). Homotype examined in Townes
Collection, 1980. Synonymized by Oehlke, 1966.
Pimpla laevifrons Thomson, 1877. Opusc. Ent., 8: 750. %, 2.
Lectotype (labelled by Aubert, 1968) 2, ''Norl'’ (Lund). Synonymized
with texana by Townes, 1944.
Taxonomy: Walkley, 1960: 365. Oehlke, 1966: 816. Aubert,1979: 73.
This species is rather characteristic in having a smooth face, convex
clypeus, convex temple and malar space about as long or longer than the basal
width of mandible. The ovipositor tip (fig. 52) assigns it to the Mandibularis
Group.
Female: Basal two flagellar segments hairy and with very few sensillae.
Head a little narrowed ventrally. Malar space 1.0 to 1.2 as long as the basal
width of mandible, longest among the species of Delomerista. Clypeus basally
convex, smooth. Face smooth, subpolished, with a few minute scattered punc-
tures. Frons, vertex and temple smooth. Temple slightly more convex and
wider than in other species. Thorax subpolished. Mesopleurum smoother
than in other species, with only minute scattered punctures. Metapleurum
finely granular, at least on apical half. Propodeum granulose in pleural area,
second lateral area, and in petiolar area. Areola elongate, roughly triangular,
narrowed and rounded basally. Costula faintly indicated or partly indistinct.
Nervellus intercepted at lower 0.33 to 0.5. First tergite angled dorsally,
where median carinae almost end. Lateral carina more or less complete.
Postpetiole laterally granuloso-rugose. Abdomen finely granular with apical
tergites becoming shagreened or coriaceous. Ovipositor stout, short, 0.7to
0.8 the length of abdomen, tip heavy, thick, (fig. 52).
Black. Malar space and mandible pale yellow. Clypeus brownish. Tegula
black, sometimes partly yellow. Legs reddish-brown with apices of hind femur
V. Gupta: Genus Delomerista (Ichneumonidae) 29
and tibia and all tarsi fuscous to black. Color of hind tibia varying from wholly
black to wholly reddish-brown (particularly in European specimens). Wings
lightly clouded (European specimens) or darker fuscous (American specimens).
Apical fuscous marks on hind femur often light to absent.
Male: Face black with whitish marks on sides (face of males of other
species wholly yellowish-white). Clypeus yellowish-white. Coxae black.
Trochanters fuscous. Propodeum wholly granulose. Costula usually distinct.
Abdomen more shagreened and coriaceous than granulose.
Length: 2, 7.5to10.5mm. Fore wing 6.0-9.0 mm. Ovipositor 5.0-6.0
mm. o, 5.5-9.9 mm. Fore wing 4.5-8.0 mm.
Specimens: Europe: ''Norvegia E., Hemnesberget Ranen’’, 12 (cotype of
D. strandi), 13-VII-1903, Coll. Strand (Berlin). Several males and females
from Alaska, British Columbia, Manitoba, Maine, New Hampshire, Quebec,
Northwest Territory, and Yukon Territory.
Host: Aubert (1969) mentions Rhyacionia buoliana as a host.
Distribution: Europe.
16. DELOMERISTA LONGICAUDA Kasparyan
This species is characterized by having a very long ovipositor, which is
about 2.0 as long as abdomen and longer than the body length. The ovipositor
tip is also characteristic (fig. 53). The ovipositor tip places it under the
Mandibularis Group.
Female: First flagellar segment with few sensillae (fig. 55). Face wider
than long, smooth, subpolished, with a few indistinct scattered punctures.
Malar space 0.5+ the basal width of mandible. Clypeus flat, smooth. Frons,
vertex and temple smooth. Thorax subpolished. Mesoscutum more hairy than
mesopleurum and metapleurum, which are beset with scattered setiferous
punctures. Propodeum subpolished, finely rugulose apicolaterally, or largely
smooth and shiny. Pleural area of propodeum rugulose. Areola horse-shoe
shaped, often open basally or apically, smooth. Costula indistinct. Second
lateral area of propodeum a little depressed, smooth to somewhat wrinkled.
Petiolar area smooth or with a few wrinkles. Nervellus intercepted at lower
0.3. First tergite 1.5 to 1.75 as long as wide, evenly convex dorsally, finely
granuloso-rugulose to shagreened, its lateral carina weak, but distinct beyond
the spiracle, its median carinae weak. Second and third tergites shagreened to
granulose. Apical tergites shagreened to coriaceous. Ovipositor long, about
2.0 as long as abdomen, and longer than the body, curved upwards, more so in
apical 0.2. Its tip demarcated by a shallow constriction (fig. 53), swollen
preapically, with upper valve wider and with a long apical slope.
Two subspecies are recognized: Delomerista longicauda longicauda
Kasparyan from USSR and D. longicauda americana from North America.
The two differ mainly in coloration of legs and tegula, and also show minor
differences in the sculpture of propodeum and abdomen.
Key to the subspecies of Delomerista longicauda
1. Tegula black. Legs including hind femur, yellowish-brown. Hind tibia
and tarsus fuscous. Propodeum subpolished and finely rugulose in
petiolar and second lateral area. Basal three abdominal tergites
granulose. USSR. ... 16a. longicauda longicauda Kasparyan (p. 30)
30 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Tegula yellow. Legs yellowish-brown but fore leg brownish-black.
Middle and hind legs beyond trochanters blackish-brown (blackish marks
on middle and hind femur varying in extent). Propodeum shiny with
second lateral area and petiolar area largely smooth. Basal three
abdominal tergites finely ruguloso-granulose, leaning toward shagreened.
North America. .... 16b. longicauda americana, n. subsp. (p. 30)
16a. DELOMERISTA LONGICAUDA LONGICAUDA Kasparyan
Delomerista longicauda Kasparyan, 1973. Zool. J., 52: 1877. ¢. des.
fig. Type ¢, Russia (Leningrad). Paratype examined, 1980.
Taxonomy: Kasparyan, 1977: 72. .
Female: A paratype from Russia has been examined and the chief diag-
nostic features are given in the key to subspecies. The first tergite is stocky
and its lateral carina is indistinct in the specimen before me.
| Distribution: Russia.
16b. DELOMERISTA LONGICAUDA AMERICANA, n. subsp. (figs. 53, 55, 56)
Female: Characterised as inthe key. Black. Malar space, mandible,
hind corner of pronotum, and tegula, whitish-yellow. Fore leg brownish-black
with yellow marks on underside of femur, tibia, and trochanters. Middle coxa
and trochanters yellowish-brown. Middle femur, tibia and tarsus fuscous.
Tibia often yellowish marked. Hind coxa, trochanters, and base of femur
yellowish-brown. Femur otherwise, tibia and tarsus blackish-brown. Base
of tibia and tarsus yellowish-white.
Male: Face white, about 1.5 as wide as long, shiny, with minute punc-
tures. Malar space black, 0.33 the basal width of mandible. Scape and
pedicel black. Propodeum subpolished, finely rugulose around carinae.
Abdomen mat to shagreened. Postpetiole with a median depression.
Median carinae on first tergite indistinct. Fore coxa white. Middle and
hind coxae brownish. Fore and middle femora, tibiae and tarsi fuscous
marked, with a white base color. Hind femur usually largely black or
blackish, though the extent variable. Hind tibia black with a ventral white
mark. Hind tarsus black.
Length: ¢, 8-10 mm, Fore wing 6.5-9 mm. Ovipositor 8-1ll m.
$, 1-8 mm. Fore wing 6-7 mm.
Holotype 2, Alaska: Anchorage, 6 to 12-VII-1976, Peter A. Rush
(Townes).
Paratypes: Alaska: Anchorage, °, 25 to 30-VI-1976; “, 11 to 18-
VI-1976, Peter A. Rush (Townes). Tsaina River, ¢, 18-VIII-1973, H. &
M. Townes (Townes). British Columbia: Stone Mt. Park at 3800+ and
5500 ft., 3°, 100%, 13 to 20-VII-1973, H. & M. Townes (Townes).
Host: Unknown.
Distribution: Alaska and British Columbia in Northwestern Nearctic
Region.
ACKNOWLEDGMENT
I am thankful to Dr. Henry Townes for providing me with the neces-
sary facilities to undertake this work and for his advice.
10.
11.
12.
13.
V. Gupta: Genus Delomerista (Ichneumonidae) 31
REFERENCES
Aubert, Jacques-F. 1969. Les Ichneumonides Ouest-Palearctiques et
leurs hotes. 1. Pimplinae, Xoridinae, Acaenitinae. Ouvrage
Publee avec le Concours du CNRS, p. 1-304. 3
Aubert, Jacques-F. 1972. Etude Commentee de Nouveaux Lectotypes
Choisis dans les Collections Holmgren et Thomson (Hym. Ichneu-
monidae). Ent. Scand. 3: 145-152.
Carlson, R. W. 1979. Family Ichneumonidae. Im Krombein ¢é ai. :
Catalog of Hymenoptera in America North of Mexico 1: 315-740.
Constantineanu, M. I. & Pisica, Constantin, 1977. Fauna Republicii
Socialiste Romania. Insecta, Hymenoptera, Ichneumonidae
9(7): 1-310.
Finlayson, Thelma 1960. Taxonomy of Cocoons and Puparia, and
their Contents, of Canadian Parasites of Neodiprion sertifer (Geoff.).
Canad. Ent. 92: 20-47. |
Finlayson, Thelma 1967. Taxonomy of Final Instar Larvae of the
Hymenopterous and Dipterous Parasites of Acrobasis spp.
(Lepidoptera: Phycitidae) in the Ottawa Region. Canad. Ent.
99: 1233-1271.
Fitton, M. G. 1976. The Western Palaearctic Ichneumonidae
(Hymenoptera) of British Authors. Bull. Brit. Mus. (Nat. Hist. )
Ent. 32(8): 303-373.
Fitton, M. G. 1978. Family Ichneumonidae. Jn Kloet and Hincks:
A Check List of British Insects, 2nd Edition. Handbooks for
Identification of British Insects, Vol. 11 (4, Hymenoptera): 12-45.
Royal Ent. Soc. London.
Fluiter, H. J. de, 1932. Bijdrage tot de Kennis der Biologie en
Epidemiologie van de gewone Dennenbladwasp, Pteronus (Lophyrus)
pint L. in Nederland. Tijdschr. Plantz. 38: 125-196.
Furniss, R. L. & Dowden, P. B. 1941. The Western Hemlock Sawfly
Neodiprion tsugae Middleton, and its parasites in Oregon. J. Econ.
Ent. 34: 46-52.
Griffiths, K. J. 1960. Parasites of Neodiprion pratti banksianae.
Rohwer in Northern Ontario. Canad. Ent. 92: 653-658.
Horstmann, K. 1981. Typenrevision der von Karl Hedwig Beschriebenen
Arten und Formen der Familie Ichneumonidae (Hymenoptera). Ent.
Mitt. Zool. Mus. Hamburg 7(112): 65-82.
Kasparyan, D. R. 1973. A New Species of the Genus Delomeyvista
(Hymenoptera, Ichneumonidae) (in Russian). Jool. Z. 52: 1877-
1878,
32
14,
15.
16.
17.
18.
19.
20.
21.
22.
23.
24,
20.
26.
27.
28.
Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Kasparyan, D. R. 1977. Review of the European Species of Ichneu-
monids of the Genus Delomerista Foerster (Hymenoptera, Ichneu-
monidae). (in Russian). New and Little-Known Species of Insects
of the European part of USSR. Acad. Sci. USSR. 1979: 69-75.
Kolomiets, N. G. 1962. Akad. Nauk SSSR Sibirskoe Otd. Parazishi
i Khishchniki Sibirskogo Shelkopryada, p. 99.
Morris, K. R. S., Cameron, E. & Jepson, W. F. 1937. The Insect
Parasites of the Spruce Sawfly (Diprion polytomum Thg.) in
Europe. Bull. Ent. Res. 28: 341-393.
Oehlke, J. 1966. Die in Europaischen Kiefernbuschhornblattwespen
(Diprionidae) Parasitierenden Ichneumonidae. Beitr. z. Ent.
15(7-8): 791-879 (1965).
Oehlke, J. 1967. Westpalaartische Ichneumonidae I: Ephialtinae. In
Junk: Hymenopterorum Catalogus (nova editio) Part 2: 1-48.
Short, J. R. T. 1978. The Final Larval Instars of the Ichneumonidae.
Mem. Amer. Ent. Inst. 25: 1-508 (Delomerista, p. 25).
Sitowski, L. 1925. Do Biologji Pasorzytow borecznixa (Lophyrus Latr.),
sur la Biologie des Parasites de Lophyrus Latr. Poln. m. Dtsch.
Zuzammenf, 14: 1-25,
Torgersen, T. R. 1969. Hymenopterous Parasites of the Hemlock Sawfly,
Neodiprion tsugae Middleton, in Southern Alaska with a key to Larval
Remains. J. Ent. Soc. Brit. Columbia 66: 53-62,
Townes, H. K. 1944. A Catalog and Reclassification of the Nearctic
Ichneumonidae. PartI. Mem. Amer. Ent. Soc. 11(1): 1-477.
(Delomerista, pp. 48-49).
Townes, H. and M. 1960. Ichneumon-flies of America North of Mexico:
2. Subfamilies Ephialtinae, Xoridinae, Acaenitinae. U. S. Natl.
Mus. Bull. 216(2): 1-676.
Townes, H., Momoi, S. & Townes, M. 1965. A Catalog and Reclassifica-
tion of Eastern Palearctic Ichneumonidae. Mem. Amer. Ent. Inst.
5: 1-661.
Townes, H. 1969. The Genera of Ichneumonidae, PartI. Mem. Amer.
Ent. Inst. 11: 1-300.
Ulbricht, A. 1911. Ichneumonidenstudien. Arch. Naturg. 77(1 Bd. 2
Heft): 144-152.
Ulbricht, A. 1913. Ichneumoniden der Umgegend Krefelds II. Nachtrag.
Mitt. Naturw. Mus. Stadt. Crefeld. 1913: 1-17.
Walkley, LuellaM. 1960. The genus Delomervisia. In Townes & Townes:
Ichneumon-flies of America North of Mexico: 2. U. S. Natl. Mus. Bull.
216(2): 362-373.
33
Genus Delomerista (Ichneumonidae)
V. Gupta
Til.
tes I,
i
II
Terg
?
es Il
D,
Tergit
2,
Propodeum.
?
4
1
Propodeum.
1,
pfankuch
1
D
6
ta nov
is
igs. 4
F
ip.
ipositor t
Figs. 1-3. Delomer
3, Ov
6, Ov
ip.
ipositor t
34 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Figs. 7-9. Delomerista borealis: 7, Propodeum. 8, Tergites II, III.
9, Ovipositor tip.
V. Gupta: Genus Delomerista (Ichneumonidae) 35
Figs, 10-20. Delomerista kusuoi: 10, Propodeum. 11, Tergites II, III.
12, Flagellar segments II, TI. 17, Ovipositor tip. 18, Flagellar segment I,
D, lepteces: 13, Propodeum, 14, Tergites II,III. 15, Flagellar segment I.
16, Ovipositor tip. 19, Flagellar segments II, III. D. pfankuchi: 20, Flagel-
lar segment I.
36 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Figs, 21-25. Delomerista walkleyae: 21, Propodeum. 22, Tergites II,
Ill. 23, Ovipositor tip. 24, Flagellar segmentI. 25, Flagellar segments II,
Ill, Figs. 26-28, D. townesorum: 26, Flagellar segmentI. 27, Flagellar
segments II, III. 28. Ovipositor tip.
37
Genus Delomerista (Ichneumonidae)
V. Gupta
a GRas
om
se eee
mM
oS
~~ SH
oh
D6
oy
=
H >
es,
es
oD or
ae)
go
De
a n
oF
2
— =
on:
oO op
NX Oo
wn
Sa
ao
s %
Ae
=
[xy
S uw
23
"s
~
v e
Ss
Le
Y Oo
ay
laa)
> a
=
or an}
NS
~—@
wn
Es}
Tr, Fe
ay
ise)
:
Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
38
ip.
Tergites 0, II.
tor t
oped
N
O
a,
opt
>
ae) a“
co
eave
5
oF
3.4
rs)
ae
&
ee
ae
se,
=e
oO
3: ae
Qi ¢,
SO
bs aD
QE o
oe
Y fa
su °
~ ped ry
eS
Aes
Gos
es
oS
on
oat A
&
bp 8
fg COD
ee
oot
cr) Fy
V. Gupta: Genus Delomerista (Ichneumonidae) 39
Figs. 40-46. Delomerista indica: 40, 41, Propodeum,. 42, 43, Tergite I.
44, Ovipositor tip. 45, Flagellar segments I,II., 46, Flagellar segments IJ, II.
40 Contrib. Amer. Ent. Inst., vol. 19, no. 1, 1982
Figs. 47-54, Delomerista strandi: 47, 51, Ovipositor tip. 54, Propodeum
and first tergite. D. mandibularis: 48, 49, Ovipositor tip. 00, Propodeum
and first tergite. D. laevis: 52, Ovipositor tip. D. longicauda americana: 03,
Ovipositor tip.
4]
Genus Delomerista (Ichneumonidae)
V. Gupta
Ay
Ly,
?
60,
da
57
Z
~1caUu
. strand
Segment I
Segments II, III.
D
?
lil
tS?
Delomervista long
59
bular
62,
3
61, Segment I,
Segments II,
mandi
wn
a)
S
¢
@
mo Q
Be:
=a +
ona
aoe
4 Ww .
agas
ae ©
Haas
ea &
Og Pa
AR
Pa es @ 5s
co WO p=
y ie os
LO nw
>
-§22
D-oee
ae
mS eS
2 & &
SAM
42
Contrib. Amer. Ent. Inst., vol. 19,
Figs. 63-65.
Delomerista japonica
Larval heads of: 63, Delomerista no vita
diprionis. 64, D. japonica
no. 1, 1982
64, D.
A REVISION OF THE GENUS AGONOCRYPTUS
(HYMENOPTERA: ICHNEUMONIDAE)
by
Santosh Gupta *
American Entomological Institute
Ann Arbor, Michigan, 48105
Agonocryptus Cushman, 1929, belongs to the tribe Gabuniini of the sub-
family Mesosteninae. It was originally proposed for Mesostenus discoidaloides
Viereck, 1905, from Kansas, U.S.A., which happens to be the only Nearctic
species to date under the genus. The genus, however, is widespread in the
Neotropical Region. In addition to the type-species mentioned above, Cushman
(1929) also placed Mesostenus (Mesostenus) chichimecus Cresson, 1873 from
Mexico and Cryptus heathi Brues, 1912 from Brazil under this genus. Subse-
quently five additional species were transferred to it: Mesostenus (Mesostenus)
‘admirandus Cresson, 1873 from Mexico by Townes (1946), M. varus: Brulle,
1846 from Guiana, and M. physocnemis Brulle, 1846, M. luxuriosus Taschen-
berg, 1876, and M. violascens Taschenberg, 1876 from Brazil, by Townes and
Townes (1966). They also synonymized M. luxuriosus with physocnemis. Thus
a total of seven species are so far known from the Nearctic and Neotropical
regions.
In the present paper 18 new species and 6 new subspecies are described
from the Neotropical Region. The types of all but those of Taschenberg and
one of Brulle (physocnemis, supposedly lost) have been studied. A. violascens
(Taschenberg) is not included as I could not find diagnostic characters in the
original description for inclusion in the key. A. discoidaloides is considered a
subspecies of chichimecus. Thus a total of 24 species and 7 subspecies are
treated in the present paper.
Genus AGONOCRYPTUS Cushman (fig. 1)
Agonocryptus Cushman, 1929. Proc. U. S. Natl. Mus., 74(16): 6.
Type: (Mesostenus discoidaloides Viereck) = chichimecus discoidaloides;
original designation.
Taxonomy: Townes and Townes, 1962: 502. Townes and Townes, 1966:
128.
Body 8-18 mm. long. Clypeus small, its basal half convex and apical por-
tion flattened, its apical margin truncate, with or without a median tooth. Man-
dible short, narrow apically, its lower tooth always longer than the upper. Face
usually trans-striate. Occipital carina may or may not reach hypostomal carina.
Mesoscutum smooth, punctate or rugoso-punctate. Epomia present or absent.
Sternaulus weak, reaching middle coxa. Prepectal carina usually 0.8 to 0.9 the
height of mesopleurum (except in A. admivandus Cresson, where it is only 0.5
the height of mesopleurum). Pleural carina of propodeum absent. Apical trans-
verse carina complete or interrupted medially. Basal transverse carina always
* Present address: Center for Parasitic Hymenoptera, Dept. of
Entomology & Nematology, Univ. of Florida, Gainesville, FL 326ll.
a Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
complete and evenly arched. Propodeal spiracle small, roundish. Propodeum
_ between the two transverse carinae variously sculptured. Areolet small, pen-
tagonal to rectangular (wider than high), sometimes a little trapezoidal. Nervu-
lus always basad of basal vein. Second recurrent vein meeting areolet at its
middle to apical 0.33. Nervellus intercepted at its middle to upper 0.33.
Petiole stout to slender, in female 2.0 to 3.0 as long as its apical width, its
sternite 0.4 to 0.75 the length of first tergite. First tergite without sub-basal
lateral triangular tooth. In bicolor with a ventrolateral tooth on either side.
Dorsolateral carina of first tergite usually absent, sometimes in traces near
its base. First tergite smooth and shiny, impunctate to strongly punctate.
Second tergite impunctate to punctate. Ovipositor tip usually with six teeth.
Tip of lower valve of ovipositor with a dorsal lobe enclosing the upper valve.
Hosts: Host records are known only for Agonocryptus chichimecus.
Podosesia syringae, Eupogonius vestitus and Psyvassa unicolor, are the hosts
of A. chichimecus discoidaloides, and Aerenicopsis championi of A. chichimecus
chichimecus.
Six species groups are recognized, based on the sculpture of frons, vertex,
and mesoscutum, length of petiole, and position of first abdominal sternite
relative to the tergite.
List of species of Agonocryptus reported in the paper:
I. The Chichimecus Group
la. chichimecus chichimecus (Cresson) Mexico
1b. chichimecus discoidaloides (Viereck) U.S.A.
2. bicolor, new species Mexico
3. vuficrus, new species Mexico
4. rufithorax, new species Brazil
5 russulus new species Brazil
Il. The Physocnemis Group
Brazil, Argentina
Brazil, Argentina ?
Argentina, Brazil
Ecuador
Central Argentina
Northern Argentina
6a. physocnemis physocnemis (Brulle)
6b. physocnemis nigristernum, new subspecies
Ta. lioneli lioneli, new subspecies
Tb. lioneli coxinota, new subspecies
8a. argentinus argentinus, new subspecies
8b. argentinus tucumanus, new subspecies
Il. The Heathi Group
9. heathi (Brues) Brazil
IV. The Varus Group
10a. A. varus varus (Brulle) French Guinea, Panama
10b. A. varus nigrifemur, new species Argentina
11. <A. rufigaster, new species Surinam.
12a. A. adustus adustus, new subspecies Peru, Brazil, Ecuador
12b. A. adustus paulus, new subspecies Colombia, Ecuador
13. A. gossypii, new species Brazil
14a. A. leurosus leurosus, new species Brazil
14b. A. leurosus flavosternum, new subspecies Paraguay, Argentina,
Bolivia
15.
24.
S. Gupta: Genus Agonocryptus (Ichneumonidae) 3
A. erugatus, new species Panama, Colombia
V. The Amoenus Group
A. admirandus (Cresson) Mexico
A. amoenus, new species Brazil
A. bispotus, new species Mexico
A. tricolor, new species Brazil
VI. The Rugifrons Group
A. rugifrons, new species Argentina
A. mulleus, new species Argentina
A. infuscatus, new species Brazil
A. fumosus, new species Brazil, Argentina
Group ?
A. violascens (Taschenberg) Brazil
KEY TO THE SPECIES GROUPS AND SPECIES OF AGONOCRYPTUS
Frons smooth and shiny, often with a few scattered punctures or dull
impunctate (argentinus). First abdominal tergite impunctate, or with
a few punctures subapically or apicolaterally. Vertex usually smooth
and shiny, sometimes with a few minute punctures (in heathi vertex
granulose and in chichimecus area behind ocelli punctate). ..... 2
Frons strongly punctate to rugoso-punctate. First tergite wholly closely
punctate. Vertex punctate. (Face always rugoso-striate, epomia
alwave abment. Rie rone Grow. oe kia ees we ee ee eee 27
Prepectal carina extending only half the height of mesopleurum. Vertex
and frons shiny, impunctate. Mesopleurum and metapleurum shiny
with separated minute punctures. Propodeum striate. Mesoscutum
with a few scattered punctures. First tergite shiny, impunctate.
Petiole long, slender, in female nearly 3.0 as long as its apical width.
First sternite 0.7 as long as petiole. Amoenus Group. Mexico.
16. admirandus (Cresson) (p. 31)
Prepectal carina extending up to 0.8 the height of mesopleurum or up to
the base of subtegular ridge. Vertex, mesopleurum, propodeum and
abdominal tergites variously sculptured. ........2.seeeecee 3
Mesoscutum punctate or rugoso-punctate. Vertex granulose or shiny with
scattered minute punctures. Propodeum basad of basal carina punctate,
sometimes punctures running into striations. ...........e-.
Mesoscutum smooth and shiny, impunctate, sometimes only basally with
a few punctures. Vertex shiny. Propodeum basad of basal carina shiny
or with few punctures or fine striations. Body generally shiny. .. 16
4 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
4. Vertex dull granulose (sometimes appearing mat). Mesoscutum moderately
punctate. Basal area of propodeum with yellow elongated mark.
(Occipital carina joining hypostomal carina at a distance almost equal
to the basal width of mandible. Lower portion of occipital carina wavy.
Fore wing with dark band at apex and just before stigma. All abdominal
tergites with yellow apical bands). Heathi Group. Brazil.
9. heathi (Brues) (p. 20)
Vertex (including ocellar area) polished and impunctate or area behind
ocelli punctate. Mesoscutum punctate to rugoso-punctate. Basal area
of propodeum without any yellow Mark. . 0 8. we cw kw ke te we 5)
5. Mesoscutum (at least the middle lobe) strongly and densely punctate,
punctures coalescing and tending to be rugose, or sometimes mat
areas seen on lateral lobes. Tooth on apical margin of clypeus absent
or minute. Occipital carina never touching hypostomal carina or in
chichimecus very close or weakly touching. Basal flagellar segments
rounded, not flattened. Apical transverse carina of propodeum usually
complete and distinct or only medially interrupted. Male flagellum
devoid of hairs and bristles (except for the regular minute pilosity).
Nervellus intercepted at the middle, except in rufithorax. Chichimecus
foe Eee Oe ae ere ge or ee ee 6
Mesoscutum punctate, punctures well separated, often with smooth areas
in the middle and on lateral lobes. Tooth on apical margin of clypeus
always present and distinct, though small. Occipital carina either
meeting hypostomal carina or strongly bent inwards and coming very
close to hypostomal carina but not touching it (physocnemis). Basal
flagellar segments moderately flattened. Apical transverse carina of
propodeum distinct only laterally and broadly interrupted medially.
Male flagellum with small hairs and with stout small bristles in between.
Nervellus intercepted above the middle. Physocnemis Group. ... Il
(I. Chichimecus Group)
6. Thorax wholly reddish-brown, without any marks. Abdomen red or black
with reddish marks. Face trans-striate. Clypeus laterally striate.
Epomia absent or faintly indicated in middle of pronotal sulcus. ... 7
Thorax black with extensive yellow marks. Abdomen black with yellow
bands, or reddish with yellow bands. Face dull or smooth in the middle,
obliquely striate laterally. Clypeus shiny, without striations. Epomia
PROCCRES se ER Se WO ee OG ee ee we ee ee 8
7. Areolet rectangular, closed, wider than high. Wings hyaline, without any
brown marks. Abdomen dorsally black, with reddish brown marks.
Nervulus intercepted above its middle. Brazil.
4. rufithorax, n. sp. (p. 13)
Areolet more squarish, as wide as high, second intercubitus unpigmented
(areolet open), intercubiti convergent. Fore wing with fuscous marks
medially and apically. Abdomen reddish-brown, without distinct black
marks. Nervellus intercepted at its middle. Brazil.
5. russulus, n. sp. (p. 13)
10.
1.
S. Gupta: Genus Agonocryptus (Ichneumonidae) 5
Abdomen reddish-brown, with yellow apical bands. All coxae reddish-
brown, rest of the legs yellowish-brown. Scape red. First abdominal
tergite punctate centrally. Mesopleurum closely and deeply punctate.
iON a 8 A ee ee $. “rufierus, ne‘sps (p. 42)
Abdomen black, with yellow bands. Hind coxa black with yellow marks.
Femora usually black marked, except in A. chichimecus discoidaloides.
Scape black, with or without a white mark. First tergite smooth and
shiny, or punctate apicolaterally. Mesopleurum with punctures which
are quite separate (A. bicolor), or punctato-striate
CA. CRICRINMBEUEI OE TRE PROP I OE I I ae Ss 9
Frons smooth or with scattered punctures. First tergite stouter, bent
medially and punctate apicolaterally. Mesopleurum punctate to rugoso-
punctate. Metapleurum rugose to rugoso-punctate (punctate in smaller
specimens). Apical propodeal carina broadly arched, complete or
incomplete medially (in type of chichimecus complete and double bent
medially). Hind femur reddish-brown or black dorsally and partly on
the inner side. U. S. A. and Mexico.
1. chichimecus (Cresson) .... 10
Frons rugulose. First tergite narrower apically, smooth, its base slender
and with a pointed tooth on either side subbasally. Mesopleurum largely
shiny, with minute punctures. Metapleurum punctate, punctures well
separated. Apical transverse carina of propodeum broadly arched and
very narrowly interrupted medially. Hind femur black dorsally.
MICE FOIE OO Og PA, 2. bicolor, n. sp. (p. WU)
Hind femur black-marked dorsally. Hind trochanters black-marked. Hind
femur comparatively thicker in the middle. Mesopleural punctures
often coalescing. Metapleurum more rugoso-punctate than punctate
(sculpture similar to that of propodeum). Male with all abdominal
tergites black-banded. Mexico.
la. chichimecus chichimecus (Cresson) (p. 10)
Hind femur and trochanters uniformly orange-brown (similar to tibia).
Femur slender. Mesopleural punctures separated from each other.
Metapleurum more punctate than rugose (sculpture weaker than that of
propodeum). Male with apical abdominal tergites reddish. U.S. A.
1b. chichimecus discoidaloides (Vier.) (p. 11)
(II. Physocnemis Group)
Occipital carina interrupted near hypostomal carina, bent inwards. Frons
minutely punctate. Subapical flagellar segments not compressed,
about 2.0 as long as wide. Rather stout species with yellow marks on
thorax and second tergite. (Mark on pronotal collar in female inter-
rupted medially). Brazil and Argentina.
6. physocnemis (Brulle)... . 12
Occipital carina meeting hypostomal carina. Frons smooth. Subapical
flagellar segments compressed, about as long as wide. Moderately
stout species with thorax yellow marked, the pronotal mark complete,
or slender species with reddish ‘thorax. 6 62.6 eee ee a 13
12.
13.
14.
15.
16.
Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
Mesosternum white marked. First tergite basally reddish to yellow.
Clypeal groove usually not black marked. Fore and middle coxae white
or white-marked. .. 6a. physocnemis physocnemis (Brulle) (p. 16)
Mesosternum black, without white marks. First tergite basally black.
Clypeal groove black marked. Fore and middle coxae black to largely
DlaCK. ose ees - 6b. physocnemis nigristernum, n. subsp. (p. 17)
Wings clear hyaline, only the apex of fore wing a little fuscous. Thorax
black, marked with yellow. Mesopleurum minutely punctate and shiny.
, Ecuador, Brazil, and Argentina.... 7¢. lioneli, n. sp. .. ... . 14
Wings wholly purple-brownish or fore wing with brownish bands. Thorax
largely red to largely black, without yellow marks. Mesopleurum punc-
tate to punctato-striate. Argentina. . 8. argentinus, n. sp..... 15
Hind coxa and middle coxa reddish-orange. Pronotal collar wholly yellow.
Second and third abdominal tergites without yellow and black marks.
Pronotum mostly punctate. Argentina and Brazil.
7a. lioneli lioneli, n. subsp. (p. 17)
Hind coxa and middle coxa yellow, with black marks. Yellow mark on
pronotal collar interrupted. Second and third tergites without yellow or
black marks. Pronotum mostly punctato-striate. Ecuador.
Tb. lioneli coxinota, n. subsp. (p. 18)
Wings wholly smoky brownish-black with a purple tinge. Mesopleurum
largely punctate or in larger and darker specimens somewhat striate.
Hind tibia black on apical 0.15 to 0.2. Scape and pedicel reddish-brown.
Central Argentina. ... 8a. argentinus argentinus, n. subsp. (p. 19)
Wings hyaline. Fore wing with two brownish bands separated by a hyaline
area. Mesopleurum striato-punctate. Hind tibia black on apical 0.35.
Scape and pedicel black. Northern Argentina.
8b. argentinus tucumanus, n. subsp. (p. 20)
First abdominal segment of female 2.0 to 2.4 x as long as its apical width,
quadrangular in cross-section at subbasal region, its sternite extending
up to 0.4 to 0.6 the length of tergite, usually to the level of spiracle.
First sternite separated from its tergite by a ridge. First tergite with
ventrolateral triangular projections at base (sometimes weak). Post-
genal area evenly arched and not separated by a crease from the lower
part of gena. Occipital carina not strongly deflected inwards and point
ing towards base of mandible, away from hypostomal carina and touch-
ing it only in gossypii. Varus Group. . . 2. ees we ew ew eee 17
First abdominal segment long and slender, in female 3.0 x as long as its
apical width, rounded in cross-section at subbasal region, its sternite
extending up to 0.75 the length of tergite. First sternite and tergite
fused together, without any trace of ventrolateral carina except in
tricolor, where ventrolateral projections are seen at base. Postgenal
area somewhat flattened and widened and separated from the lower por-
tion of gena by a crease (in profile view). Occipital carina deflected
inwards either strongly or weakly, coming close to joining hypostomal
carina or erased for a distance equal to the basal width of mandible.
PIIOenas CLO. Ce er a ea ee ee le ee ee 29
17.
18.
10.
20.
21.
S. Gupta: Genus Agonocryptus (Ichneumonidae) 7
(IV. Varus Group)
Abdomen impunctate and polished. First abdominal sternite short of the
level of spiracle, 0.4 the length of tergite. Propodeum basad of basal
carina smooth and shiny. Abdominal tergites sparsely hairy dorsally,
except tips of seventh and eighth. Body rather stout. Panama and
Colomiyiay 26 690 eR ee, 15. erugatus, n. sp. (p. 29)
Abdomen with punctures, at least on second and third tergites laterally.
First abdominal sternite extending up to the level of spiracle or slightly
beyond it. Basal area of propodeum trans-striate (except in adustus).
Fourth and following tergites rather uniformly hairy dorsally, with
their margins fringed with hairs, especially seventh and eighth. Body
Slender. 5 SS Oe I PE a a 18
Pronotum striate, particularly along the sulcus and along posterior margin.
Pronotal collar and upper margin with scattered punctures. First
sternite ending at the level of spiracle and 0.5 the length of tergite.
Areolet 1.5 to 1.75 as wide as high. Brazil, Paraguay, Bolivia, and
APOENIMNA ea a IS 4 14. leurosus, n. sp..... 19
Pronotum punctate to mat. Pronotal collar sometimes smooth and
polished. First sternite either ending at the level of spiracle or extend-
ing slightly beyond it, 0.5 to 0.6 the length of tergite. Areolet 1.25 to
1.5 AB WIDE BSA ee ee ae Ses 20
Mesosternum and middle coxa dorsally black. First tergite wholly reddish.
Brasil F Be Ss 14a. leurosus leurosus, n. subsp. (p. 28)
Mesosternum with yellow marks. Middle coxa dorsally red. First tergite
with apical and basal yellow marks and medially usually blackish, some-
times second tergite with blackish marks. Paraguay, Bolivia, and
Arconting.< ser. . 14b. leurosus flavosternum, n. subsp. (p. 28)
Thorax wholly yellowish-brown and abdomen from second segment onwards
brownish-black. Wings tinged with fuscous brown. Male abdomen
yellowish-brown, as is thorax. Flagellar segments not flattened and
without long hairs. Small sized species. Brazil.
13. gossypii, n. sp. (p. 26)
Thorax black with yellow marks. Abdomen reddish-brown. Wings clear
hyaline, with or without fuscous patches. Basal flagellar segments in
female usually flattened. Male flagellum usually with long hairs. . 21
Propodeum largely smooth, with weak to indistinct striations, particularly
on the basal area. Apical transverse carina indistinct, or if faintly
indicated, more semicircular, like carinae bordering petiolar area.
First sternite 0.6 the length of tergite, ending slightly beyond the level
of spiracle. Fore wing with fuscous bands at middle and at its apex.
Peru, Brazil, Ecuador, and Colombia.
12. ‘adustus, ne spy. 6 22
Propodeum largely strongly striate to rugoso-striate. Apical transverse
carina distinct, strongly arched medially. First sternite 0.5 to 0.6
the length of its tergite. Fore wing with or without fuscous bands. . 23
22.
23.
24,
20.
Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
Face finely striate. First tergite, hind coxa, trochanters, and femur
reddish-brown, without any marks. Hind tibia and tarsus yellow with
fourth tarsal segment apically and fifth either partly or wholly brownish.
Pronotal collar wholly yellow. Apex of fore wing very lightly fuscous.
Basal flagellar segments flattened (as usual). Size 8-14 mm. Peru,
Brazil and Ecuador. .... 12a. adustus adustus, n. subsp. (p. 25)
Face smooth and shiny, without striations. First tergite apically and
basally yellow. Hind coxa, femur and trochanters reddish-brown with
fuscous marks. Apex of hind femur blackish. Hind coxa with a dorsal
yellow line. Hind tibia and tarsus yellow, but fourth and fifth tarsal
segments black. Apical fuscous mark on fore wing more conspicuous.
Yellow mark on pronotal collar interrupted medially. Basal flagellar
segments not conspicuously flattened. Size 10 mm. Colombia and
POUACOP es ks e ee 12b. adustus paulus, n. subsp. (p. 26)
Propodeum strongly rugose medially. Petiolar area with vertical striations.
First sternite extending beyond the level of the spiracle, 0.6 the length
of its tergite. Pronotum irregularly punctate, the groove along its hind
margin wrinkled. Areolet rectangular, about 1.5 as wide as high.
Mesoscutum with yellow crescentic mark on side of lateral lobe. Yellow
mark on pronotal collar interrupted medially. Surinam.
11. rufigaster, n. sp. (p. 23)
Propodeum striate. Petiolar area of propodeum smooth to dull mat. First
sternite ending at the level of spiracle. Pronotum with minute punctures,
shiny, the groove along its hind margin smoother. Areolet more
squarish, about 1.2 as wide as high. Lateral lobes of mesoscutum
without any yellow marks. Yellow mark on pronotal collar not inter-
rupted mediallvic caw Gua aaa GS 10. varus (Brulle).... 24
Femora yellowish-brown. Yellow mark on pronotal collar interrupted
medially. Abdomen yellowish-brown. French Guiana and Panama.
10a. varus varus (Brulle) (p. 22)
Fore and middle femora ventrally and hind femur wholly black. Pronotal
collar wholly yellow. Abdomen reddish-brown. Argentina.
10b. varus nigrifemur, n. subsp. (p. 23)
(Vv. Amoenus Group)
Occipital carina making a right angle with hypostomal carina, strongly
deflected towards base of hypostomal carina, away from the base of
mandible by 1.5 the basal width of mandible. Abdomen smooth and
shiny, impunctate. Tergites without hairs. Basal area of propodeum
with conspicuous semicircular striations. Brazil.
17. amoenus, n. sp. (p. 32)
Occipital carina normal, making an angle of less than 499 with the hyposto-
mal carina and joining it. Occipital carina not deflected towards base of
hypostomal carina, running towards base of mandible, but often erased
(except in tricolor, in which propodeum smoother). Abdomen with
setiferous punctures and apical tergites hairy. Basal area of propodeum
without striations, often punctate laterally. ......-..+e-se-eee 26
S. Gupta: Genus Agonocryptus (Ichneumonidae) 9
26. Epomia present. Propodeum apicad of basal carina with strong striations
and punctures in between. Abdomen banded with black and yellow.
NIG. ison iva deh ined See Macelantd in 18. bispotus, n. sp. (p. 33)
Epomia absent. Propodeum with broken to indistinct striations apicad of
basal transverse carina. Abdomen reddish, without stripes. Brazil.
19. tricolor, n. sp. (p. 34)
(VI. Rugifrons Group)
27. Wings hyaline. Face strongly rugose in the middle. Clypeus granulose with
a few punctures. Thorax black, with yellow marks. Abdomen reddish-
brown or body wholly reddish-brown. ... 1... 2. ee ee ee ees 28
Wings strongly infuscate. Face rugoso-striate. Clypeus finely striate.
Thorax reddish-brown, without any marks. Abdomen black with reddish
VOR TESS 6 oak esta has. Bb lacs Debate ie ae aa RRs be ee ain 29
28. Thorax black with yellow marks. First tergite white apically. Tarsal
segments of middle leg reddish-brown to brownish-black. First tergite
closely punctate. Occipital carina meeting hypostomal carina.
APU a ek th a ee a Rees 20. rugifrons, n. sp. (p. 35)
Body wholly reddish-brown. First tergite apically not white. Tarsal
segments of middle leg white. First tergite only centrally with sparse
punctures. Occipital carina not meeting hypostomal carina.
POO eis cas +k shin Tews aK | 21. mulleus, n. sp. (p. 36)
29. Occipital carina not meeting hypostomal carina. Face reddish-brown,
without yellow orbital rings. Apical 0.6 of first tergite and hind femur
black. Second and third tarsal segments of hind leg yellow. Brazil.
22. infuscatus, n. sp. (p. 36)
Occipital carina meeting hypostomal carina. Face black, with broken yellow
orbital rings. First tergite, hind coxa and hind femur reddish-brown.
In addition to second and third segments, the apical 0.6 of first tersal
segment of hind leg yellow. Argentina and Brazil.
23. fumosus, n. sp. (p. 37)
I. THE CHICHIMECUS GROUP
This group is characterized by having the frons smooth; vertex generally
smooth with minute scattered punctures or punctures closer behind ocelli;
occipital carina almost touching to widely separated from hypostomal carina,
not deflected inwards; tooth on apical margin of clypeus absent or minute; basal
flagellar segments of female antenna not compressed; flagellar segments in
male devoid of long hairs (males of only chichimecus and russulus are known);
pronotum striate to striato-punctate; epomia absent or present; mesoscutum
strongly to densely punctate; punctures coalescing and tending to be rugose;
propodeum punctate basally, rugoso-striate medially, its apical transverse
carina present, complete or broken medially; abdomen strongly punctate.
The nervellus is intercepted at the middle, except in rufithorax.
This group includes five species: A. chichimecus (Cresson) from the U.S.
A. and Mexico, and four new species, bicolor and ruficrus from Mexico and
rufithorax and russulus from Brazil (maps 1, 2).
A. chichimecus and bicolor are distinctive by the absence of tooth on
10 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
clypeal margin and by the presence of epomia. The body is marked with yellow.
They can be differentiated among themselves by the nature of frons, apical
transverse carina of propodeum, shape and punctation of first tergite, and by
the color of hind leg. A. vufithorax and A. russulus are distinctive in having
reddish thorax and abdomen, without yellow marks, meso- and metapleurum
punctate, clypeal margin with a minute tooth, and by the absence of epomia.
They can be differentiated among themselves by the nature of areolet, markings
on wings, and by the position of nervellus. A. rvussulus is the only species with
fuscous marks on the fore wing in the female. A. ruficrus has many characters
in common with A. chichimecus and bicolor, but abdomen is reddish-brown,
coxae reddish-brown, and clypeal margin with a minute tooth.
1. AGONOCRYPTUS CHICHIMECUS (Cresson)
Female: Face shiny with a few trans-striations below antennal sockets to
granulose with submedian oblique striations. Clypeus shiny, without any punc-
tures or striations, its apical margin truncate, without a median tooth. Malar
space granulose, nearly equal to the basal width of mandible. Temple shiny,
impunctate. Frons shiny, with a few fine superficial punctures in ocellar area.
Vertex shiny, closely punctate behind ocelli. Occipital carina close to hyposto-
mal carina and separated from it by a distance equal to 0.25 to 0.5 the basal
width of mandible. Pronotum punctate to striate, its hind margin and pronotal
sulcus striate. Epomia present, strong or weak. Mesoscutum closely and
deeply punctate. Prepectal carina reaching subtegular ridge. Scutellum
sparsely punctate. Mesopleurum punctate to rugoso-punctate, punctures close
(punctate in smaller specimens). Metapleurum rugose to rugoso-punctate.
Apical transverse carina of propodeum broadly arched, complete or incomplete
medially. Propodeum strongly punctate to rugoso-punctate, centrally more
rugose, its petiolar area with irregular striations or longitudinal ridges.
Areolet trapezoidal to pentagonal (first intercubitus shorter than the second).
Second intercubitus pigmented or unpigmented. Second recurrent vein meeting
areolet at its apical 0.4 to 0.3. Nervellus intercepted at its middle. Petiole
stout, its sternite reaching the spiracle. First tergite shiny, punctate dorso-
laterally. Second and third tergites wholly closely and finely punctate. The
following tergites punctate. Ovipositor 0.6 to 0.7 the length of abdomen. |
Two subspecies, A. chichimecus chichimecus (Cresson) and A. c. discoi-
daloides (Viereck) (New Status) are recognized.
la. AGONOCRYPTUS CHICHIMECUS CHICHIMECUS (Cresson)
Mesostenus (Mesostenus) chichimecus Cresson, 1873. Proc. Acad. Nat.
Sci. Philadelphia, 1873: 155. °. key, des. Lectotype: ¢, Mexico:
Orizaba (Philadelphia). Mexico: Cordoba. Type examined.
Mesostenus chichimecus: Cresson, 1916. Mem. Amer. Ent. Soc., 1: 23.
Lectotype designation.
sel Se ae chichimecus: Cushman, 1929. Proc. U. S. Natl. Mus.,
74(16): 7. syn. Townes, 1946. Bol. Ent. Soc. Venezolana, 5: 34.
Townes, 1966. Mem. Amer. Ent. Inst., 8: 128.
Male and Female: Punctures on mesopleurum often coalescing. Meta-
pleurum rugoso-punctate. Hind femur thicker than in discoidaloides. Black,
with yellow marks and bands on abdomen. Face, clypeus, labrum, a mark on
base of mandible, orbital ring, temple broadly, a mark on mesoscutum,
scutellum, metascutellum, propleurum, upper margin of pronotum, pronotal
collar completely or interrupted medially, tegula, subtegular ridge, speculum,
S. Gupta: Genus Agonocryptus (Ichneumonidae) 11
a large mark covering most of mesopleurum, mesosternum large, a mark
below wings, metapleurum, and a dagger-shaped mark on petiolar area of pro-
podeum, yellow. Wings hyaline. Legs yellow. Fore femur ventrally and fore
tarsus brown. Hind coxa basally and with an oblong mark dorsally, trochanters
partly, and femur dorsally, black. First tergite apically and basally, and the
following tergites apically and laterally yellow.
Length: 11-16mm. Fore wing 8-12 mm.
Specimens examined: 229, 40°. Mexico: Orizaba, 1¢ (lectotype). Mexico:
Cordoba, 1¢ (labelled paratype). [Specimens bear label only as Mexico.
Locality data are in the original descriptions]. Mexico: 1% (paratype,
Washington). Mexico: San Rafael, Jocoltepec, 12. Ticul Yucatan, 3%, June
1969, CIBC, €x Cerambycid on Eupatorium odovatum. Vera Cruz, 3°, 2°, ex
Aerenicopsis championi, Krauss, No. 5776. Vera Cruz, Ver., 6°, May 1959,
N. L. H. Krauss: 12, June 1955, ex Aerenicopsis championi. Ma Cambo,
Vera Cruz, Ver. 12, June 1965, N. L. Krauss ex Aerenicopsis championi in
branch of Lantana camara. Vera Cruz., Ver., 4°, 2%, May 1955, ex
Aerenicopsis championi burrows in Lantana camara (all Washington).
Host: Aerenicopsis championt.
Distribution: Mexico.
1b. AGONOCRYPTUS CHICHIMECUS DISCOIDALOIDES (Viereck), new status
Mesostenus discoidaloides Viereck, 1905. Trans. Kansas Acad. Sci.,
19: 319. ¢. Type: 2, Rock Creek, 900 ft., Douglas Co., Kansas
(Lawrence).
Agonocryptus discoidaloides: Cushman, 1929. Proc. U. S. Natl. Mus.,
74(16): 6. Townes and Townes, 1962. Bull. U. S. Natl. Mus.,
216(3): 502. des., fig.
Female: Punctures on mesopleurum a little separated from each other.
Metapleurum more punctate than rugose. Clypeal groove and base of clypeus
usually black. Second intercubitus pigmented. Hind femur and trochanters
uniformly orange brown.
. Male: Slender. Structure similar to that of female except that pronotum is
shiny, without striations or punctures and punctation of mesopleurum and meta-
pleurum a little sparse and superficial. Apical abdominal tergites usually
reddish. First abdominal tergite basally black. Hind tibia apically darker.
(In chichimecus chichimecus all abdominal tergites are black, banded with
yellow. )
Length: 10-18mm. Fore wing 6-14 mm.
Specimens examined: U. S. A: Alabama (Gulf Shores). Florida (Key
Largo, Larkins, Paradise Key, Tarpon Springs). New Jersey (Moorestown).
New York (Farmingdale). North Carolina (Wake Co.). South Carolina
(McClellanville). Wisconsin (Milwaukee).
Hosts (From Carlson's Catalog): Podosesia syringae, Eupogonius
vestitus, Psyvassa unicolor. |
Distribution: U. S. A.: Southeastern United States, Texas, Kansas,
and some localities in Midwestern States. Distributional Map 288 in Townes
and Townes, 1962.
2. AGONOCRYPTUS BICOLOR, n. sp.
Female: Face centrally smooth and shiny, laterally with a few oblique
12 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
striations. Clypeus smooth and shiny, its apical margin truncate, without a
median tooth. Malar space granulose, 1.0 the basal width of mandible. Temple
shiny, impunctate. Frons rough or rugulose, a little densely rugulose in
ocellar area. Vertex medially punctate. Occipital carina close to hypostomal
carina and separate from the latter by a distance about half the base of mandible.
Pronotum punctate above, striate in the sulcus, striate along margins. Epomia
present. Mesoscutum deeply and closely punctate. Prepectal carina reaching
close to subtegular ridge. Mesopleurum minutely punctate, with shiny areas
between punctures. Area below subtegular ridge with a few striations. Meta-
pleurum punctate, punctures well separated. .Propodeum with narrowly inter-
rupted apical transverse carina which is strongly curved submedially. Basal
area of propodeum striato-punctate. Area between the two transverse carinae
punctato-striate. Petiolar area punctate, with a few longitudinal ridges.
Areolet pentagonal. Second recurrent vein meeting areolet in the middle.
Nervellus intercepted at its middle. Petiole moderately stout, its base slender
and with a ventro-lateral tooth on either side. First sternite reaching apical
0.4 of petiole. First tergite smooth and shiny, with a few scattered punctures.
Second and the third tergites basally and medially closely and deeply punctate.
The following tergites finely mat.
Black, with yellow marks and bands. Face, broad orbital rings, clypeus
except margins, temple, base of mandible, and labrum, yellow. A mark on
upper margin of pronotum, pronotal collar, mark on propleurum, central mark
on mesoscutum, scutellum, metascutellum, tegula, subtegular ridge, specu-
lum, a large mark covering most of mesopleurum, mesosternum, a mark below
wings, metapleurum, and an inverted T-shaped mark on petiolar area of pro-
podeum, yellow. Legs yellow with black marks. Fore femur dorsally and
tarsus brownish. Middle coxa ventrally with a basal black mark. Middle femur
and tibia ventrally, and tarsus, brown. Hind coxa basally and dorsally black
marked. Trochanters and femur dorsally black. Wings hyaline. First tergite
apically and the following tergites apically and laterally, yellow.
Male: Unknown.
Length: 19mm. Fore wing 12 mm.
Holotype: ¢, Mexico: Oaxaca, Metate, 85 kilometers south of Tuxtepec,
9000 m., Oct. 20, 1962, H. & M. Townes (Townes).
Distribution: Mexico (map 1).
3. AGONOCRYPTUS RUFICRUS, n. sp.
Female: Face dull, with a few punctures and oblique striations submedially.
Clypeus dull, its apical margin with a minute tooth. Malar space granulose,
0.9 the basal width of mandible. Temple shiny, impunctate. Frons with a few
minute scattered punctures. Vertex with fine punctures in ocellar area.
Occipital carina close to hypostomal carina and separated from it by a distance
of 0.25 the basal width of mandible. Pronotum deeply punctate, its hind mar-
gin and sulcus with striations. Epomia present, though not complete. Meso-
scutum closely and deeply punctate. Scutellum deeply but sparsely punctate.
Mesopleurum closely and deeply punctate. Metapleurum with irregular punc-
tures, punctures close and deep. Propodeum rugoso-punctate to rugose, its
apical transverse carina broadly interrupted medially. Areolet slightly trape-
zoidal, second recurrent vein meeting areolet at its apical 0.4. Nervellus
intercepted at its middle. Petiole stout, its length less than 2.0 the apical
width of first tergite, its sternite reaching the spiracle. First tergite punctate
centrally. Second and third tergites closely punctate. The following tergites
finely mat. Ovipositor 0.9 the length of abdomen.
S. Gupta: Genus Agonocryptus (Ichneumonidae) 13
Black with yellow marks. Abdomen reddish with yellow bands. Scape
reddish-brown. Face, clypeus except its apical margin, labrum, base of
mandible, broad orbital rings, and temple, yellow. Upper margin of pronotum,
pronotal collar, propleurum, a mark on mesoscutum, scutellum, metascutel-
lum, tegula, subtegular ridge, speculum, mesopleurum broadly, mesosternum,
area below wings, metapleurum wholly, and a large dagger-shaped mark on
propodeum extending up to basal transverse carina, yellow. Wings slightly
clouded apically. Legs reddish-yellow. First tergite apically and basally,
and the following tergites apically, with yellow bands.
Male: Unknown.
Length: 16mm. Fore wing 12 mm.
Holotype: ¢, | Baja California, Mexico]: San Jose del Cabo (Washington).
Distribution: Mexico (map 1).
4. AGONOCRYPTUS RUFITHORAX, n. sp.
Female: Face granulose with striations submedially and a few scattered
punctures laterally. Clypeus granulose, laterally finely striate, its apical
margin with a minute median tooth. Malar space obliquely aciculate, 0.8 the
basal width of mandible. Temple smooth and shiny. Frons shiny, with fine
punctures close to ocelli. Vertex shiny, with a few fine superficial punctures.
Occipital carina directed towards base of mandible and separated from the
latter by a distance about equal to the basal width of mandible; this area finely
striate. Pronotum striato-punctate, its hind margin striate. Epomia absent.
Mesoscutum closely and deeply punctate. Scutellum with fine, deep punctures.
Prepectal carina reaching subtegular ridge. Mesopleurum and metapleurum
closely and deeply punctate. Propodeum deeply punctate, . punctures running
into transverse striations. Petiolar area sparsely punctate, with a few lateral
longitudinal ridges. Apical transverse carina present, but a little irregular
submedially. Areolet rectangular, closed, wider than high. Second recurrent
vein meeting areolet at its middle. Nervellus intercepted above the middle.
Petiole moderately long, not very stout, 2.0 as long as its apical width,
smooth and shiny and with a few fine superficial punctures. Second and third
tergites closely and finely punctate. The following tergites finely mat. Ovi-
positor 0.7 the length of abdomen.
Brownish-red. Abdomen brownish-black. Interrupted orbital rings, basal
half of clypeus, and labrum, yellow. Wings hyaline. Legs reddish-brown.
Middle tibia lighter in color. Hind femur and tibia black. Hind tarsus yellow.
Second and following abdominal tergites blackish with reddish-brown marks
submedially.
Male: Unknown.
Length: 12-15 mm. Fore wing 8-10 mm.
Holotype: 2, Brazil: Nova Teutonia, Santa Catarina, April 13, 1948,
Fritz Plaumann (Townes).
Pavatypes: 392, Brazil: Nova Teutonia, Santa Catarina, Feb. 1946 and
Dec. 1970 (Townes). Nova Teutonia, 279 11' B. 52° 23' L., 300-500 m., 19,
Nov. 1966, Fritz Plaumann (Ottawa). 3
Distribution: Brazil (map 2).
0. AGONOCRYPTUS RUSSULUS, n. sp.
Female: Face and clypeus finely striate. Apical margin of clypeus trun-
cate and with a minute median tooth. Malar space granulose, equal to the basal
14 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
width of mandible. Temple shiny. Occipital carina directed towards base of
mandible and separated from the latter by a distance equal to the basal width of
mandible; this area finely striate. Frons shiny and with a few superficial punc-
tures. Pronotum punctate with a few oblique striations, its hind margin striate.
Epomia absent. Mesoscutum, mesopleurum, and metapleurum punctate. Scu-
tellum sparsely punctate. Propodeum basally rugoso-punctate, medially
rugoso-striate. Petiolar area somewhat irregularly striate. Areolet squarish,
as wide as high, intercubiti convergent, but second intercubitus largely unpig-
mented (areolet open). Second recurrent vein meeting areolet at its middle.
Nervellus intercepted at its middle. First tergite slender, punctate apicolater-
ally, its sternite reaching the spiracle. Second and third tergites closely and
finely punctate. The following tergites finely mat. Ovipositor 0.8 as long as
the abdomen.
Reddish-brown. Median flagellar segments, a mark on labrum (and some-
times on clypeus), interrupted orbital rings, a mark on pronotal collar, upper
edge of pronotum, tegula, and subtegular ridge, white. Ventral aspect of first
trochanter of fore leg, and hind tarsus, white. Middle coxa and femur, hind
coxa, trochanters, femur and tibia, and abdominal tergites apically, brownish.
Wings hyaline and with brownish marks apically and medially.
Male: Antenna spinose, with small fine hairs inbetween. Face and clypeus
finely striate, punctate inbetween. Frons granulose with fine transverse acicu-
lations. Vertex shiny, sparsely superficially punctate. Pronotal collar
sparsely superficially punctate, its groove shiny and without striations or punc-
tures. Mesoscutum closely superficially punctate. Mesopleurum shiny. Meta-
pleurum with a few superficial punctures. Apical and basal transverse propodeal
carinae complete and strong. Basal area of propodeum close to spiracle irregu-
larly punctate, its lateral area inbetween the two transverse carinae rugose and
medially with a few trans-striations. Petiolar area shiny, with two longitudinal
striate, one on each side of middle. Second recurrent vein meeting areolet at
its apical 0.3.
Yellowish-brown. Tenth to fifteenth flagellar segments yellow. Face,
clypeus, labrum, base of mandible, temple broadly, interrupted orbital rings,
propleurum, pronotal collar, tegula, subtegular ridge, a mark on scutellum,
fore coxa and trochanter, and hind tarsus yellow. Second and following abdom-
inal tergites basally, hind tibia apically, and first hind tarsal segment darker.
Wings hyaline.
Length: 10-15mm. Fore wing 8-12 mm.
Holotype: °, Brazil: Santa Barbara, Minas Gerais, Serra do Caraca,
Jan. 1970, Oliveira (Townes).
Allotype: %, Same locality and data as the type (Townes).
Paratypes: 3%, 3%. Brazil: Same locality as the type, 1600 m., 1%, 18,
Jan. 1970 and Feb. 1969, F. M. Oliveira. Guanabara, Represa Rio Grande,
1°, March 1972, M. Alvarenga. Murique, Rio de Janeiro, Mangaratiba, 19,
July, 1969, M. Alvarenga. S. J. Barreiro, Sao Paulo, Serra da Bocaina,
1650 m., 2°, Nov. 1969, M. Alvarenga and Seabra (Townes).
Variations: Two males from Bocaina are a little darker than the others,
especially the mesoscutum and pronotum.
Distribution: Brazil (map 2).
S. Gupta: Genus Agonocryptus (Ichneumonidae) 15
Ul. THE PHYSOCNEMIS GROUP
This group is characterized by having the frons smooth and shiny; vertex
with a few scattered minute punctures behind ocelli; occipital carina meeting
hypostomal carina or bent inwards and close to it but not actually touching it
(bhysocnemis); clypeus with a median tooth along its apical margin; basal
flagellar segments somewhat compressed; pronotum striate in middle and punc-
tate along upper and hind margins; epomia present but not complete; meso-
pleurum punctate but punctures well separated; metapleurum punctate; pro-
podeum basally strongly punctate; apical transverse carina distinct only later-
ally, broadly interrupted medially; and abdomen punctate. The male flagellum
is beset with small hair with stout bristles in between. The nervellus is inter-
cepted above the middle.
The Physocnemis Group includes three species: A. physocnemis (Brullé)
from Brazil and Argentina; A. lioneli from Argentina, Brazil and Ecuador;
and A. argentinus from Argentina. Each species has two subspecies (map 3).
A. physocnemis has its occipital carina bent inwards, coming close to the
middle of hypostomal carina, but not meeting it, frons minutely punctate and
subapical flagellar segments not compressed. In the other two species the
occipital carina meets the hypostomal carina and the subapical flagellar seg-
ments are compressed. In A. argentinus the wings are either wholly purple-
brownish or with blackish-brown bands on the fore wing. In A. lioneli the
wings are hyaline or a little brown-tinged apically. The mesopleurum of
A. lioneli is minutely punctate and shiny, while A. argentinus exhibits varia-
tions in having punctate to rugoso-punctate mesopleurum. These two species
can be further differentiated by the color of abdomen and thorax.
6. AGONOCRYPTUS PHYSOCNEMIS (Brullé)
Female: Subapical flagellar segments not compressed, about 2.0 as long
as wide. Face granulose, with a few punctures laterally; medially and sub-
medially with fine trans-striations. Clypeus granulose, with a few impressions
of punctures or a few trans-striations laterally, its apical margin with a
median tooth. Malar space granulose. Temple shiny, finely granulose close
to malar space. Frons shiny, with minute punctures. Vertex shiny, witha
few scattered punctures behind ocelli. Occipital carina angularly bent and
coming very close to hypostomal carina, sometimes bent portion erased and
replaced by one or two striations. Pronotum deeply punctate. Pronotal collar
finely and closely punctate. Pronotal sulcus with striations. Epomia absent.
Mesoscutum punctate, with shiny areas in-between. Scutellum sparsely punc-
tate, punctures superficial. Mesopleurum punctate, but punctures in yellow
area not prominent. Area below subtegular ridge with a few trans-striations.
Metapleurum punctate. Basal area of propodeum strongly punctate to punctato-
striate. Propodeum medially rugoso-striate or punctato-striate. Apical trans-
verse carina broadly interrupted medially. Petiolar area irregularly longi-
tudinally striate. Areolet wider than high. Second recurrent vein meeting
areolet at its middle. Nervellus intercepted at its upper 0.4. Petiole stout to
very stout, its sternite 0.4 to 0.5 the length of petiole. First tergite shiny
and with a few punctures. Second and third tergites with close and fine punc-
tures. The following tergites finer and mat. Ovipositor 0.6 as long as abdo-
men.
Black, with yellow marks. Abdomen brown. Face, clypeus except its
16 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
apical margin, labrum, orbital rings, temple, propleurum apically, upper part
of pronotum, interrupted mark on pronotal collar, a mark on mesoscutum,
scutellum, metascutellum, tegula, subtegular ridge, speculum, a broad oblong
mark on mesopleurum, a mark on mesosternum (present or absent), mark on
metapleurum (except basal black band), and an inverted T-shaped mark on
apical slope of propodeum, yellow. Wings hyaline. Fore and middle legs yellow
with their coxae and femora ventrally black and tarsi brownish-black. Hind
coxa, trochanters, and femur reddish-brown, tibia and tarsus yellow. First
tergite black, with yellow marks at base and apex. (In subspecies nigristernum
yellow only apically). The following tergites brown with the second tergite
basally black and apically yellow. Sometimes third and fourth tergites also
narrowly brownish-black basally and yellow apically.
Male: Antennal flagellum with small hairs and spines in between. Prono-
tum shiny, without punctures. Otherwise sculpture similar to that of the
female.
Black with yellow marks. Resembles female with the following differences:
Pronotal collar wholly yellow. Mesopleural mark larger. Mesosternum wholly
yellow or wholly black. Wings hyaline. Fore and middle coxae and trochanters
wholly white. Hind coxa black with yellow marks. Hind femur black, yellowish-
brown basally. Hind tibia basally yellow and apically black. First tarsal seg-
ment black. Abdomen black with apical yellow bands.
Two subspecies are recognized: Agonocryptus physocnemis physocnemis
(Brulle) and A. physocnemis nigristernum, n. subsp. Their chief difference
is in the coloration of mesosternum and first tergite, as given in the key.
6a. AGONOCRYPTUS PHYSOCNEMIS PHYSOCNEMIS (Brullé)
Mesostenus physocnemis Brulle, 1846. In Lepeletier: Histoire Naturelle
des Insectes. Hymenopteres, 4: 236. @. des. Type: 2, Brazil (lost).
Mesostenus luxuriosus Taschenberg, 1876. Ztschr. f. die Gesam. Naturw.
Halle, 48:94. 2. des. Type: $, Brazil: [Nova Friburgo] (Halle).
Synonymized by Townes, 1966.
Agonocryptus physocnemis: Townes, 1966. Mem. Amer. Ent. Inst.,
Sy 126,
Characterized as under the species and in the key. This subspecies is
more reddish with fore and middle coxae white or white marked and meso-
sternum with white marks. The base of first tergite is reddish or yellow.
Length: ¢: 20-12 mm. Forewing 15-10 mm. ©: 15-12 mm. Forewing
6-8 mm.
Specimens examined: 219, 8%. Brazil: Linhares, Espirito Santo, 59,
60, Sept. 1972. Encruzilhada, Bahia, 980 m., 39, 1°, Nov. 1974. Represa
Rio Grande, Guanabara, 12, June 1967; 1%, Oct. 1967; 12, Jan. 1968; 1°,
March 1972; 42, May 1972. Espirito Santo, Castelo, 12, Nov. 1976; all above
collected by M. Alvarenga.Pedra Azul, Minas Gerais, 800 m., 12, Nov. 1970,
F. M. Oliveira; 22, Nov. 1971, Nov. 1972, Seabra & Olivera (Townes).
Argentina: Corrientes, Las Marias, Ca. Virasoro, 2, Nov. 10-15, 1969,
C. C. Porter (Tucuman). One specimen shows some characters of physoenemis
nigristernum. This one has not been designated paratype.
Distribution: Argentina, Northern Brazil (map 3).
S. Gupta: Genus Agonocryptus (Ichneumonidae) 17
6b. AGONOCRYPTUS PHYSOCNEMIS NIGRISTERNUM, n. subsp.
This subspecies is differentiated from the typical subspecies in having the
first tergite basally black, clypeal groove black marked, mesosternum black,
without yellow marks and fore and middle coxae black. Otherwise agrees with
the typical subspecies. The two subspecies intergrade in Argentina and further
study may reveal that the two segregats may not have yet assumed subspecific
status.
Length 2: 20-12 mm. Fore wing 15-10 mm. ©: 10-15mm. Fore wing
0-8 mm.
Holotype: ¢, Brazil: Campina Grande, (near Curitiba), Feb. 15, 1966,
H. & M. Townes (Townes).
Allotype: %, same locality and data as the holotype (Townes).
Pavatypes: 102, 6°. Brazil: Same locality as the holotype, 1°, Feb. 17,
1966, H. & M. Townes (Townes). Curitiba, 19, 1%, Jan. 20-31, 1969, L. J.
Stange. Nova Teutonia, Santa Catarina, 3°, 9°, collected on various dates
from March to December by Fritz Plaumann. Floresta da Tijuca, Guanabara,
1°, Apr. 1966, Alvarenga & Seabra (Townes). Nova Teutonia, 300-500 m.,
19, Oct. 28, 1957; 19, Oct. 30, 1958, Fritz Plaumann (Ottawa).
Distribution: Southern Brazil, ?Argentina. (map. 3).
7. AGONOCRYPTUS LIONELI, n. sp.
Female: Subapical flagellar segments compressed, about as long as wide.
Face and clypeus mat, with fine sparse punctures. Face with a few trans-
striations in-between. Apical margin of clypeus with a median tooth. Malar
space aciculate, equal to the basal width of mandible. Temple shiny. Frons
shiny, impunctate. Vertex shiny, impunctate. Occipital carina touching
hypostomal carina. Pronotum punctate to punctato-striate. Pronotal collar
and upper part of pronotum with fine punctures. Pronotal sulcus with a few or
more striations. Epomia faintly indicated. Mesoscutum shiny, its middle lobe
sparsely punctate and lateral lobes closely punctate with shiny central areas.
Scutellum with a few superficial punctures. Mesopleurum shiny, punctate to
minutely punctate. Metapleurum with close and deep punctures. Basal area of
propodeum punctate, its central area rugoso-striate. Propodeum between the
two trans-carinae rugose and in the yellow area trans-striate to rugose.
Petiolar area longitudinally striate. Areolet a little wider than high. Second
recurrent vein meeting areolet at its middle or in its apical 0.4. Nervellus
intercepted at its upper 0.4. Petiole stout. First sternite reaching up to the
spiracle of first tergite. First tergite shiny, with or without a few fine punc-
tures apicolaterally. Second and third tergites closely and finely punctate.
The following tergites mat.
Two subspecies, A. lioneli lioneli, from Argentina and Brazil, and
A. lioneli coxinota, from Ecuador, are recognized by the characters mentioned
in the key.
Ta. AGONOCRYPTUS LIONELI LIONELI, n. subsp.
Female: Pronotum largely punctate, only with a few striations in the
pronotal sulcus. Punctures on mesopleurum fine and a little apart. Propodeum
centrally rugose, but its yellow area mostly trans-striate. First tergite with
a few fine punctures apicolaterally.
18 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
Black. Head and thorax black with yellow marks. Abdomen yellowish-
_ brown to reddish-brown, with black and yellow marks. Face, clypeus except
apical margin, labrum, temple, orbital rings, pronotal collar, upper part of
pronotum, propleurum apically, a mark on mesoscutum, scutellum, meta-
scutellum, tegula, subtegular ridge, speculum, a large oblong mark on meso-
pleurum, a mark on mesosternum, a mark below wings, a mark on metapleur-
um, and a dagger-shaped mark on the apical slope of propodeum, yellow.
Wings hyaline, with brownish marks medially and apically. Legs yellowish.
Fore coxa, trochanters, and femur ventrally black-marked. Middle coxa
reddish-orange, and femur ventrally black. Hind coxa, trochanters, and femur
reddish-orange, its tibia and tarsus yellowish-brown. Abdomen reddish-
brown to brown. First tergite apically and basally yellow, black in the middle,
laterally brownish-red. Second and third tergites without yellow and black
marks.
Male: Flagellar segments hairy and with spines. Male more shiny than
the female, with pronotum with a few punctures on the lower side only. Apical
transverse carina of propodeum strong. Second abdominal tergite medially,
and third only basally, punctate.
Black with yellow marks. Color of head and thorax similar to that of female
except that yellow mark on pronotal collar is interrupted. Hind coxa black with
white marks, its trochanters, femur and tibia reddish-brown, and tibia apically
and first tarsus basally brown. Rest of hind tarsus white. Fore and middle
coxae white with blackish marks baso-dorsally, trochanters yellow, darker
dorsally, femora and tibiae yellowish-brown, and tarsi brownish. Abdominal
tergites 1-3 basally black. Tergites 1-2 apically yellow. Rest of abdomen
reddish-brown.
Length: 10-18mm. Fore wing 7-13 mm.
Holotype: ¢°, Argentina: Tucuman, 11 kilometers west of Las Cejas,
March 9-April 11, 1968, Lionel Stange (Townes).
Allotype: &%, Same locality and data as the holotype, (Townes).
Paratypes: 132, 25°. Argentina: Same data as the holotype, but collected
on different dates from February to April, 52, 21% (Townes). Positos, Salta,
12, 2%, Jan. 1971, M. A. Fritz (Townes). Brazil: Colatina, Espirito Santo,
1°, Oct. 1969, F. M. Oliveira. Bahbalha, Ceara, 400 m., 1%, May 1969,
M. Alvarenga (Townes). Santo Grande, 2¢, 1968, M. Fritz (Townes). Argen-
‘tina: Corrientes, Las Marias, Ca Virasoro, 1°, Nov. 10-15, 1969, C. Porter.
Salta. Rte 34, 12 km. NE Urundel-Arroyo Riacho Seco, 2°, July 24-29, 1978,
Porter and Fidalgo (Porter). Salta, Rio Pescado Ca., 1°, Feb. 19, 1959,
Atmat Bennagar (Porter). Isla, Martin Garcia, 1%, Jan. 1971, H. Zimmer-
mann (Washington).
Distribution: Argentina and Brazil (map 3).
Tb. AGONOCRYPTUS LIONELI COXINOTA, n. subsp.
Female: Pronotum mostly punctato-striate. Punctures on mesopleurum
closer and deeper. Propodeum centrally rugose, including the yellow area.
First tergite mostly impunctate.
Color similar to that of lioneli lioneli, except that the yellow mark on
pronotum interrupted, middle and hind coxae yellow and black marked ventrally,
second and third tergites with black subbasal and yellow apical marks.
Male: Unknown.
Length: 18mm. Fore wing 12-13 mm.
Holotype: 2, Ecuador: San Rafael, 200 m., 1930, Campos R. (Washington).
Distribution: Ecuador (map 3).
S. Gupta: Genus Agonocryptus (Ichneumonidae) 19
8. AGONOCRYPTUS ARGENTINUS, n. sp.
Female: Subapical flagellar segments compressed, about as wide as long.
Face dull, weakly to moderately striate. Clypeus dull, mat with a few lateral
striations. Malar space aciculate mat, 0.9 times the basal width of mandible.
Frons dull, slightly protuberant in the middle. Temple shiny, impunctate.
Vertex shiny, with a few minute scattered punctures. Occipital carina meeting
hypostomal carina. Pronotum punctate. Pronotal sulcus striate. Epomia
indistinct, sometimes faintly visible in the sulcus. Mesoscutum with scattered
punctures on the middle lobe, its lateral lobes sparsely punctate with smooth
central areas. Scutellum with scattered punctures, which are close in the
apical half. Mesopleurum punctate to punctato-striate in larger and darker
specimens. Metapleurum rugose to reticulato-rugose. Petiolar area of pro-
podeum longitudinally striate. Apical transverse carina broadly interrupted
medially. Areolet rectangular. Second recurrent vein meeting areolet at its
middle or in apical 0.45. Nervellus intercepted at its upper 0.4. Petiole
stout, its sternite reaching spiracle. Postpetiole with scattered punctures.
Second and third tergites closely punctate. The following tergites finely
punctate to mat. Ovipositor 0.6 to 0.7 as long as the abdomen.
Reddish-brown to black. Scape and flagellum reddish-brown to black.
Flagellar segments 6-10 white. Head reddish-brown. Apex of mandible,
malar space, temple medially, and area just below antennal sockets, black.
Inner orbital rings, incomplete outer orbital rings, labrum, and a mark on
clypeus, yellow. Thorax reddish-brown. Pronotal collar, middle lobe of
mesoscutum medially, tegula, subtegular ridge, lower portion of mesopleurum,
mesosternum, area behind wings, metapleurum, and propodeum dark brown.
Sometimes pronotal collar, mesoscutum, mesopleurum, and mesosternum,
reddish-brown. A specimen from Potrerillos, Mendoza, with thorax wholly
black, while in some other specimens from Cordoba, thorax black with reddish
marks on various parts. Wings smoky brownish-black with purple tinge or
hyaline. Fore wing with broad apical and medial dark brown bands. Fore,
middle and hind coxae, and trochanters reddish-brown, with a few fuscous
marks. All femora and tibiae yellow with blackish marks on tibia apically.
Fore and middle tarsi yellowish-brown. Hind tarsus black. Abdomen
brownish-black to black, with first tergite lighter in color.
The specimens exhibit considerable variations in sculpture and color.
However, two subspecies are recognized: A. argentinus argentinus from
Central Argentina, and A. argentinus tucumanus from Northern Argentina.
8a. AGONOCRYPTUS ARGENTINUS ARGENTINUS, n. subsp.
Female: Mesopleurum punctate to striato-punctate in larger and darker
specimens. Color exhibiting considerable variation as described under species
description. Scape and pedicel reddish-brown. Femur and tibia yellow, some-
times darker but not reddish brown. Tibia black in apical 0.14 to 0.12. Wings
smoky brownish-black and with a purple tinge.
Male: Unknown.
Length: 14-18 mm. Fore wing 10-13 mm.
Holotype: ¢, Argentina: Cordoba, Davis (Cambridge).
Pavatypes: 42. Argentina: Cordoba, 3°, W. M. Davis. Mendoza,
Potrerillos, 19, Feb. 20, 1966, C. C. Porter (Cambridge).
Distribution: Central Argentina (map 3).
20 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
8b. AGONOCRYPTUS ARGENTINUS TUCUMANUS, n. subsp.
Female: Mesopleurum striato-punctate. Scape and pedicel black. Face
black, with two small roundish marks just below antennal sockets. Inner
orbits, outer orbits (interrupted), and clypeus except its apical margin,
yellow. Thorax reddish-brown. Hind margin of pronotum, apical corner of
scutellum, metascutellum, tegula, subtegular ridge, mesopleural area just
below speculum, metapleurum, and central area of propodeum, brownish-
black. Petiolar area yellowish-brown. Wings hyaline, dark brown medially
and apically. Fore leg yellowish-brown, its coxa and first trochanter dorsally
blackish. Middle coxa, trochanters and femur, reddish-brown, its tibia
yellowish-brown and tarsus blackish. Middle coxa and trochanters with brown-
ish marks. Hind coxa, trochanters, and femur reddish-brown, with brownish
marks. Hind tibia yellow with its apical 0.35 black. Hind tarsus black.
Abdomen black with basal 0.5 of first tergite yellowish-brown.
Male: Unknown.
Length: 2, 17mm. Fore wing 13 mm.
Holotype: 2,-Argentina: Tucuman, 11 kilometers west of Las Cejas,
March 7-26, 1967, Lionel Stange (Townes).
Distribution: Northern Argentina (map 3).
Ill. THE HEATHI GROUP
This group is characterized by having a granulose vertex; closely punctate
mesoscutum, with smooth areas in between; and strongly punctate metapleurum,
with punctures stronger than on mesopleurum. The lower portion of occipital
carina is wavy and it meets hypostomal carina at a distance equal to the basal
width of mandible. It includes only one species, Agonocryptus heathi (Brues),
which has an elongated yellow mark on basal area of propodeum and all
abdominal tergites are with yellow apical bands.
9. AGONOCRYPTUS HEATHI (Brues)
Cryptus heathi Brues , 1912. Ann. Ent. Soc. America, 5: 196. 2. des.,
fig. Type: ¢, Brazil: Guarabira (= ''Independencia"') in Paraiba
(Cambridge).
Agonocryptus heathi. Cushman, 1929. Proc. U. S. Natl. Mus., 74(16): 7.
Townes, 1966. Mem. Amer. Ent. Inst., 8: 128.
| Female: Face with semicircular striations and fine scattered punctures.
Clypeus with a few fine punctures. Malar space mat, equal to the basal width
of mandible. Frons shiny, with a few fine punctures. Vertex granulose.
Occipital carina wavy in the lower portion and meeting hypostomal carina at a
distance equal to the basal width of mandible. Pronotum punctate. Epomia
absent. Mesoscutum punctate, with shiny areas in between. Mesopleurum
finely punctate. Metapleurum more strongly punctate than mesopleurum.
Scutellum finely and sparsely punctate. Propodeum basally closely and deeply
punctate, centrally rugoso-striate. Apical transverse carina complete.
Areolet pentagonal. Second intercubitus not as strong as the first. Second
recurrent vein meeting areolet at its apical 0.4. Nervellus intercepted at its
upper 0.35. Petiolar area irregularly striate. Petiole stout, its sternite
extending up to spiracle. Petiole and postpetiole shiny, with a few impressions
S. Gupta: Genus Agonocryptus (Ichneumonidae) 21
of punctures laterally. Second and third tergites closely and finely punctate,
the following tergites finely mat.
Black. Thorax yellow marked. Abdomen yellowish-brown with yellow
bands. Face yellow with a central triangular black mark. Malar space, apex
of mandible, frons and vertex medially, black. Pronotal collar, upper edge of
pronotum, a mark on mesoscutum, tegula, subtegular ridge, scutellum, meta-
scutellum, an oblong mark on mesopleurum, a mark below wings, a mark on
mesosternum, a broad mark on metapleurum, a small mark at the center of
basal area of propodeum, and a dagger-shaped mark at the apical slope of
propodeum, yellow. Hind coxa, trochanters, femur and tibia yellowish-brown,
with tibia basally lighter and apically a little darker. Hind tarsus and a small
mark on coxa dorsally, white. Fore and middle legs largely yellowish, with
darker patches. Wings hyaline. Fore wing with dark band at apex and just
before stigma. Abdomen yellowish-brown with apical yellow bands on tergites.
Length: 12mm. Fore wing 8 mm.
Specimens examined: 22. Brazil: Independencia (Guarabira), Paraiba,
12 (type), Mann & Heath (Cambridge). Brazil: Caruaru, 900 m., 12, April,
1972, M. Alvarenga (Townes). This specimen exhibits slight variations from
the type, with face more strongly striate, a small yellow mark on side of pro-
podeum, and middle coxa with a small yellow mark.
Distribution. Brazil (map 2).
IV. THE VARUS GROUP
Related and rather similar to the Amoenus Group in having smooth frons,
mesoscutum and vertex, but the occipital carina is not strongly deflected
inwards, rather pointing towards base of mandible or towards apex of hyposto-
mal carina, always away from it by varying distances (except in gossypii).
Postgenal area not conspicuously flattened or widened, more uniformly arched
with the lower part of gena. Basal flagellar segments in female flattened (less
so in a@dustus paulus, and not so in gossypii). First abdominal segment not very
slender, in female about 2.0 to 2.4 its apical width, and quadrangular in cross-
section in subbasal region, its sternite extending up to the middle (level of
spiracle), or slightly beyond it (0.4-0.6 length of tergite). Epomia absent
(or faintly seen in adustus paulus).
The males have long hairs on flagellar segments (except in gossypii),
each segment also usually with long spine-like stout seta amongst the hairs at
the apex of segments, particularly from fourth flagellar segment onwards.
Males of most species are similar looking and not very diagnostic. They are
slender in build. They even resemble the males of the Amoenus Group.
A. gossypii is exceptional in many characters, particularly in having the
occipital carina touching the hypostomal carina, and in other characters
mentioned in parenthesis above. However, it fits better in this group than any
where else.
This group includes A. varus (Brullé), and five new species:
gossypii, adustus, erugatus, leurosus and rufigaster, all from the Neotropical
Region. Of the species placed in this group, A. evugatus is rather stout with
abdomen smooth and polished, hairs on apical tergites rather sparse dorsally,
and fourth to sixth abdominal tergites without apical fringe of hairs. The pro-
podeum basad of basal carina is smooth and shiny. A. leurosus has the pro-
notum striate and the areolet is rather wide, about 1.5-1.75 x as wide as high.
A. adustus and A. rufigastery have the first abdominal sternite extending up to
0.6 the length of tergite, but in adustus the propodeum basad of basal carina
22 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
is polished with only a few punctures or weak striations and apical transverse
carina of propodeum is indistinct, while in rufigaster the propodeum is striate
basally and rugose in the central yellow area and the apical transverse carina
is distinct. The petiolar area is with vertical striations. A. varus has the
first sternite ending at the level of spiracle, propodeum striate medially
rather than rugose, petiolar area mat, wings without fuscous marks, pronotum
mat, and areolet more squarish. Otherwise it comes close to rufigaster in the
sculpture of basal area of propodeum and in the shape of apical transverse
carina of propodeum. A. gossypii is rather distinctive. It is a small sized
Species, with occipital carina meeting hypostomal carina, and flagellar seg-
ments not flattened and without long hairs.
10. AGONOCRYPTUS VARUS (Brullé)
Female: Face with fine trans-striations. Clypeus with a few fine stria-
tions laterally. Malar space finely aciculate, equal to the basal width of man-
dible. Temple close to the malar space with a few fine aciculations. Frons
dull, without punctures. Temple and vertex shiny, impunctate. Occipital
carina away from hypostomal carina by a distance equal to 0.5 the basal
width of mandible. Pronotum smooth, with scattered punctures, groove along
its hind margin smooth. Mesoscutum, scutellum, mesopleurum and meta-
pleurum shiny, with minute setiferous punctures. Basal area of propodeum
finely striate. Central area of propodeum between the basal and apical trans-
verse Carinae trans-striate. Apical transverse carina strongly arched medi-
ally. Petiolar area smooth to dull, mat. Areolet more squarish, about 1.2 as
wide as high; second recurrent vein meeting in its middle. First abdominal
segment 2.2 as long as its apical width; its sternite ending at the level of
spiracle, about 0.5 the length of its tergite. All abdominal tergites dull, with
hairs, which become denser on apical tergites. Second abdominal tergite punc-
tate medially and third at base. Ovipositor about 0.72 the length of abdomen.
Two subspecies are recognized: A. varus varus (Brulle) and A. varus
nigrifemur, n. subsp., based upon the color of legs, pronotal collar and
abdomen, as given in the key.
A specimen from Jamaica (from Washington Museum) is damaged and has
a reddish thorax and black abdomen, and probably represents a distinct sub-
species. It is not named because of its damaged condition.
10a. AGONOCRYPTUS VARUS VARUS (Brullé)
Mesostenus varus Brullé, 1846, In Lepeletier: Histoire naturelle des
Insectes, Hymenopteéres, 4: 235. 2. des. Type: 9, Guyana"
(Paris).
Agonocryptus varus: Townes, 1966, Mem. Amer. Ent. Inst., 8: 128.
Female: Black with yellow marks; abdomen yellowish-brown. Face,
clypeus (except apical margin), labrum, orbital rings, a mark on mesoscutum,
scutellum, metascutellum, pronotal collar, upper part of pronotum, propleurum,
tegula, subtegular ridge, speculum, a mark below wings, a large oblong mark
on mesopleurum, a mark on metapleurum, and a dagger-shaped mark on apical
slope of propodeum, yellow. Legs yellow, with hind coxa, trochanters and
femur brownish. Fore coxa with a black mark at base ventrally. Wings hya-
line, without fuscous marks.
Male: Face transversely striated. Clypeus shiny. Malar space granu-
S. Gupta: Genus Agonocryptus (Ichneumonidae) 23
lose, slightly less than the basal width of mandible. Temple close to the
malar space with a few fine aciculations. Frons dull without punctures.
Temple and vertex shiny, impunctate. Occipital carina reaching the hypostomal
carina. Pronotum smooth, its upper part with close superficial punctures, its
hind margin punctate with a few striations. Mesoscutum, scutellum, meso-
pleurum and metapleurum shiny, with minute setiferous punctures. Basal
area of propodeum striate; central area of propodeum between basal transverse
and apical transverse carinae trans-striate. Apical transverse carina strongly
arched medially. Petiolar area longitudinally striate. Areolet slightly wider
than high; second recurrent vein meeting at its middle. First abdominal ter-
gite 3.5 x its tergite. Abdominal tergites shiny. Second abdominal tergite
medially and third basally punctate.
Black with yellow marks. Abdomen yellowish-brown, with black bands.
Face, clypeus, labrum, base on mandible, temple, malar space, orbital rings,
a mark on mesoscutum, scutellum, matascutellum, pronotal collar, pronotum,
(except upper sulcus) propleurum, tegula, subtegular ridge, speculum, a mark
below wing, lower part of mesopleurum, mesosternum, metapleurum anda
dagger-shaped mark on apical slope of propodeum, yellow. Legs yellow. Fore
femur and tibia dorsally with an elongate brown mark, third and fourth tarsal
segments and claws black. Middle femur and tibia dorsally with an elongate
brown mark, tarsus and claws black. Hind coxa and trochanters dorsally
black marked, femur apically and apical 0.6 of tibia and apical 0.6 of basi-
tarsus black. First abdominal tergite apically and basally and second to fifth
abdominal tergites apically with yellow bands.
Length 2: 16-20 mm. Fore wing 12-15mm. ©: 10-15mm. Fore wing
6-12 mm.
Specimen examined: 399, 2¢0°. 1 (type), (Paris). The type has no
locality label; only a green circular label, and an identification label. Panama:
Barro Colo, Is., CZ, 12, June 1940, Zetek 4669 (Washington). Tobago Is.,
12, Feb. 14, 1912, A. BusckColl. (Washington). Tobago Is., 1°, Feb. 24,
1912, 1°, Feb. 23, 1912, A. Busck Coll. (Washington).
Distribution: Panama and "'Guiana’’ (map 4).
10b. AGONOCRYPTUS VARUS NIGRIFEMUR, n. subsp.
Female: Pronotal collar wholly yellow. Mesosternum with yellow
marks. Fore leg yellow, its coxa and femur black ventrally, and tarsus
brownish. Middle coxa black with dorsal yellow mark, trochanters and
femur black, tibia yellow, tarsus brownish. Hind coxa reddish-brown, darker
ventrally, trochanters brown, femur black, tibia and tarsus yellow. Abdomen
brown with blackish areas in middle of first, second, third, and fourth tergites.
Male: Unknown.
Length: 15mm. Fore wing 10 mm.
Holotype: 2, Argentina: Salta, Route 34, 12 kilometers northeast of
Urundel-Arroyo Riacho Seco, July 24-29, 1978, Porter and Fidalgo (Porter).
Paratype: 12, Argentina: Salta, Rio Pescado, Ca Oran, May 23, 1970,
C. Porter (Porter).
Distribution: Argentina (map 4).
11. AGONOCRYPTUS RUFIGASTER, n. sp.
Female: Face with fine trans-striations. Clypeus with a few fine stria-
tions laterally and centrally with a few punctures in between. Malar space
24 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
finely aciculate, equal to the basal width of mandible. Temple close to malar
space with a few fine aciculations. Frons, vertex and temple shiny, impunc-
tate. Occipital carina very close to hypostomal carina but not meeting it.
Pronotum shiny, punctate, its hind margin smooth above, striate below.
Middle lobe of mesoscutum only basally with a few punctures. Mesoscutum
otherwise smooth and shiny. Scutellum, mesopleurum and metapleurum shiny
with minute setiferous punctures. Basal area of propodeum finely striate;
area above spiracle striato-punctate; central area of propodeum strongly
rugose; petiolar area with vertical striations; apical transverse carina distinct,
complete and strongly arched medially. Areolet 1.5 as wide as high. Second
recurrent vein meeting at its apical 0.40. Nervellus intercepted at its upper
0.40. First abdominal segment 2.2 as long as its apical width, its sternite
extending up to 0.6 its length. All abdominal tergites shiny, with hairs.
Fourth tergite onwards with an apical fringe of hairs. Second and third ter-
gites minutely and finely punctate. Ovipositor about 0. 84 the length of abdo-
men. |
Black, with yellow marks; abdomen yellowish-brown. General coloration
similar to that of A. varus. Differences are: yellow mark on pronotal collar
interrupted medially. Lateral lobes of mesoscutum with a crescentic mark.
Fore wing infuscate centrally and apically.
Male: Similar to that of A. adustus paulus in structure and color and
differs only in the lighter color of hind coxa and hind femur.
Length: 11-16mm. Fore wing 8-13 mm.
Holotype: °, Surinam: Paramaibo, malaise trap, March 2-4, 1964,
D. C. Geijskes (Townes).
Allotype: %, Surinam: 45 kilometers south of Paramairbo, Oct. 3-8,
1963, D. C. Geijskes (Townes).
Distribution: Surinam (map 4).
12. AGONOCRYPTUS ADUSTUS, sp. nov.
Female: Face granulose with submedian trans-striations or with a few
punctures. Clypeus granulose with a few superficial punctures medially.
Malar space granulose. Frons, temple and vertex shiny, impunctate.
Occipital carina away from hypostomal carina by a distance equal to the basal
width of mandible. Pronotum with scattered punctures, its scrobe long, hind
margin wrinkled. Middle lobe of mesoscutum basally punctate. Mesoscutum
otherwise smooth and shiny. Scutellum, mesopleurum, mesosternum and
metapleurum mostly shiny and with a few minute setiferous punctures. Pro-
podeum largely smooth, with weak to indistinct striations, particularly on the
basal area; apical transverse carina indistinct, if faintly indicated, more semi-
circular, like carinae bordering petiolar area. Areolet 1.3 to 1.4 as wide as
high. Second recurrent vein meeting areolet at middle or in its apical 0.3.
Nervellus intercepted at its upper 0.4. First abdominal segment 2.2 as long
as its apical width, shiny; its sternite extending up to 0.6 the length of tergite.
Second and third tergites with a few fine punctures basolaterally. The follow-
ing tergites smooth and shiny. Fourth and following tergites rather uniformly
hairy dorsally with their margins fringed with hairs, especially on seventh and
eighth. Ovipositor 0.7 the length of abdomen.
Black, the head and thorax marked with yellow and abdomen reddish-
brown. Head yellow except clypeal margin, malar space, mandible, frons and
vertex medially, and whole of occiput, black. Pronotal collar wholly yellow or
interrupted in the middle. Upper margin of pronotum, propleurum, a mark at
S. Gupta: Genus Agonocryptus (Ichneumonidae) 25
apex of middle lobe of mesoscutum, scutellum, metascutellum, tegula, sub-
tegular ridge, speculum, a mark behind hind wing, a broad and oblong mark
on mesopleurum, a large mark on metapleurum, and an inverted T-shaped
mark on apical slope of propodeum, yellow. Leg color as described under the
subspecies. Wings hyaline with fore wing marked brown medially and apically.
Abdomen wholly reddish-brown or first tergite with basal and apical yellow
marks and second tergite apically yellow, bordered with black. Tip of abdomen
fuscous.
Male: Rather thin and slender as compared to the female, with antennal
segments with long hairs and a stiff seta at apex of each flagellar segment
among the hairs. Body sculpture generally similar to that of female, but
males show considerable variation. Face shallowly punctate to trans-striate.
Frons smoother to punctate. Basal area of propodeum smooth to rough. Pro-
podeum centrally striate to rugose. Apical transverse carina distinct.
Black. Antenna wholly black. Head yellow with mandible, frons and ver-
tex medially and upper half of occiput, black. Thorax black with pronotal
collar, upper margin of pronotum, propleurum, a mark at apex of middle lobe
of mesoscutum, scutellum, metascutellum, tegula, subtegular ridge, speculum,
area behind hind wing broadly, and oblong mark on meso and metapleurum,
and petiolar area, yellow. Wings hyaline. Fore wing only apically lightly to
moderately fuscous; fore and middle coxae and trochanters yellow, their femora,
tibiae and tarsi yellowish-brown with middle tarsus blackish. Hind leg either
wholly black with coxa encircled with white, or coxa, first trochanteral seg-
ment and femur reddish-brown. Abdomen either largely black with apices of
first to third segments and sides of fourth to sixth segments yellow, or apical
half of all tergites yellowish-brown; color of hind leg and abdominal tergites
highly variable in the two subspecies described below. |
Two subspecies are recognized, which have been keyed out along with the
key to the species. A. adustus adustus occurs in Peru and at lower elevations
in Brazil and Ecuador bordering Peru southeast of the high Andes running
across Colombia and Ecuador. A. adustus paulus occurs on the Andes in
Colombia and Ecuador and also west of the same at somewhat lower elevations.
12a. AGONOCRYPTUS ADUSTUS ADUSTUS, n. subsp.
Female: Face finely shagreened with trans-striations. Basal area of
propodeum smooth and shiny, with a few fine punctures. Central area finely
to moderately striate. Pronotum with minute punctures. Basal flagellar seg-
ments somewhat flattened.
General color as described under the species. Differences and variations
are: Face with small lateral black marks just above clypeus in the paratypes.
Yellow mark along pronotal collar complete. Mesosternum black. Speculum
only with a small yellow mark. Sometimes apex of first tergite yellow. Fore
and middle legs largely yellow with coxae blackish on their posterior sides,
their second trochanteral segments and femora blackish-brown dorsally and
apical tarsal segments brownish. (In one paratype the brownish mark on
middle femur appears more ventral in position.) Hind coxa, trochanters and
femur reddish-brown, tibia and tarsus yellow with fifth and sometimes fourth
also, blackish-brown.
Male: Face shallowly striate; in one paratype smoother and with shallow
punctures. Frons punctate to smooth. Propodeum basally smooth and shiny
and centrally striate.
Mesosternum black, sometimes mesosternum yellow near middle coxa.
26 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
Hind leg wholly black or hind femur brownish-black. Fore wing of allotype
darkly fuscous apically; other paratypes with lightly to darkly fuscous fore
wing tip. Abdomen largely black with only apices of tergites brownish. Some-
times yellow marks on sides of thorax smaller.
Length: °, 8-14mm. Fore wing 6-10 mm.
Holotype: °, Peru: Avispas, 30m. nr. Marcapata, Sept. 1962, Luis Pena
(Townes).
Allotype *, same data as the holotype, except collected on Oct. 1-15, 1962
(Townes).
Paratypes: 22, 50%. Peru: Quincemil, 750 m, near Marcapata, 12, Nov.
1962; 3 %, Oct. 20-30, 1962. Avispas, 30 m. near Marcapata, 1%, Sept.
1962, all collected by Luis Pena (Townes). Brazil: Jacareacanga, Para, 19,
Dec. 1968, Moacir Alvarenga (Townes). Ecuador: Napo and Coca Rivers, 1°,
May 2-10, 1965, Luis Pefia (Townes).
Distribution: Peru, and at lower elevations in Brazil and Ecuador (map 4).
-12b. AGONOCRYPTUS ADUSTUS PAULUS, n. subsp.
Female: Basal flagellar segments not conspicuously flattened (exception,
perhaps due to smaller sized specimens). Face shiny with a few scattered
punctures, without striations; pronotum shallowly punctate and shiny. Pro-
podeum shallowly striate in the middle. Otherwise smooth and shiny.
Black. Vertex with a Y-shaped yellow mark. Mesosternum with yellow
marks. Yellow mark on pronotal collar interrupted medially. Fore and
middle legs similarly colored. Coxae and first trochanteral segments whitish-
yellow. Coxa ventrally black. Second trochanter, femur and tibia yellow,
femur dorsally brownish-black; tarsus brownish. Hind coxa, trochanters and
femur reddish-brown with fuscous marks, coxa with a dorsal yellow line, apex
of femur blackish, tibia and tarsus yellow but fourth and fifth tarsal segments
black. Apical fuscous mark on fore wing more conspicuous. First tergite
apically and basally broadly yellow. Second tergite apically yellow, subapically
black adjacent to the yellow mark.
Male: Face shallowly striate with a few punctures in between striations;
frons and pronotum smooth and shiny; propodeum centrally rugoso-striate.
Black. Mesosternum largely yellow. Hind coxa and femur reddish-brown,
trochanters and tibia black, tarsus either wholly black or third segment and
sometimes second segment partly yellow. Sometimes hind femur brownish-
black as is tibia and tarsus, but coxa always reddish-brown. Mesosternum at
least partly yellow. Abdominal segments black basally and reddish-brown
apically. First tergite yellow basally and apically and second tergite largely
black. Color otherwise similar to that of adustus adustus.
Length: 2, 10mm. Fore wing 8 mm.
Holotype: 2, Colombia: Cali, Oct. 1971, M. J. W. Eberhard (Townes).
Allotype “, same data as holotype (Townes).
Paratypes 8 %. Colombia: Cali, 3 %, same data as holotype. Ecuador:
Santo Domingo, 680 m, 3 °%, May 15-30, 1975, S. & J. Peck. Loja: Latoma,
1500 m, 2 ©, Nov. 18-19, 1970, Luis Pefia (Townes).
Distribution: Colombia and Ecuador (map 4).
13. AGONOCRYPTUS GOSSYPI, n. sp.
Female: Face granulose with a few scattered punctures. Clypeus shiny,
S. Gupta: Genus Agonocryptus (Ichneumonidae) ai
impunctate, its apical margin without a median tooth. Malar space mat, 0.6
as long as the basal width of mandible. Temple, frons, and vertex shiny,
impunctate. Occipital carina meeting hypostomal carina. Pronotum shiny,
impunctate. Epomia absent. Middle lobe of mesoscutum with a few punctures
basally. Scutellum impunctate. Mesopleurum with a few fine punctures.
Metapleurum with a little coarser punctures as compared to mesopleurum, but
punctures not deep. Propodeum basally with a few large scattered punctures.
Propodeum medially transversely rugose. Petiolar area a little smoother.
Areolet rectangular, 1.5 as wide as high. Second intercubitus absent. Second
recurrent vein meeting areolet at its apical 0.33. First abdominal segment 2.0
as long as its apical width, its sternite ending at the level of its spiracle.
First tergite shiny, impunctate. Second tergite with moderately sparse punc-
tures, punctures large. Third and fourth tergites basally with close, fine
punctures. The following tergites mat. Ovipositor 0.8 as long as the abdomen.
Yellowish-brown. Abdomen brownish-black. Head, scape, and antenna
brown, except interrupted inner and outer orbital rings. Clypeus broadly, and
labrum, yellow. Wings tinged with fuscous-brown. Legs yellowish-brown,
with middle tarsus, hind trochanters, femur, tibia, basal 0.5 of hind basitar-
sus, and fourth tarsal segment, brown. Abdomen brownish-black. First seg-
ment brownish.
Male: Generally similar to the female, the flagellar segments without long
hairs but with spines in between. Face wholly yellow. Petiolar area of pro-
podeum yellow. Hind trochanters, femur and basal 0.5 of tibia yellowish-
brown. First tergite of the same color as the rest of the abdomen.
Length: 8-10 mm. Fore wing 6 mm.
Holotype: ¢, Brazil: Sao Paulo, July 27, 1936, E. J. A. Hambleton, ex
cotton stalks infested with Gasterocercodes gossypii, No. 27 (Washington).
Allotype: ¢, same locality and data as the holotype (Washington).
Pavatypes: 19, 1%, same data as the holotype (Washington).
Distribution: Brazil (map 4).
14. AGONOCRYPTUS LEUROSUS, n. sp.
Female: Face and clypeus finely, transversely striate with punctures in
between. Malar space longitudinally aciculate and 0.9 the basal width of man-
dible. Temple close to malar space aciculate, otherwise smooth and shiny.
Frons smooth and shiny, with a few minute superficial punctures. Vertex
smooth and shiny, impunctate. Occipital carina away from hypostomal carina
by basal width of mandible, pronotum striate, particularly along the sulcus
and along posterior margin. Pronotal collar and upper margin with scattered
punctures. Mesoscutum smooth and shiny, only the basal area of middle lobe
with a few close punctures. Scutellum, mesopleurum, and mesosternum with
moderately sparse fine punctures. Metapleurum shiny, with a few fine punc-
tures to moderately deep punctures. Propodeum basally finely wholly striate,
centrally striate; petiolar area semicircularly or irregularly striate. Areolet
rather wide, about 1.5 to 1.75 as wide as high. Second recurrent vein meeting
areolet at its apical 0.4. Nervellus intercepted at its upper 0.45. First abdo-
minal segment shiny, about 2.2 as long as its apical width. First sternite
ending at the level of spiracle, 0.5 the length of tergite. Second and third ab-
dominal tergites closely, finely punctate. Abdominal tergites hairy, especially
fourth tergite onwards. Ovipositor 0.85 the length of abdomen.
Black with yellow marks. Abdomen reddish. Face, clypeus except its
apical margin, labrum, orbital ring, a triangular mark on mesoscutum, scu-
28 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
tellum, metascutellum, an interrupted mark on pronotal collar, upper margin
of pronotum, apical part of propleurum, tegula, subtegular ridge, a mark
below hind wing, a large mark on metapleurum and an inverted T-shaped mark
on apical slope of propodeum, yellow. Yellow mark on mesosternum present
or absent depending upon the subspecies. Wings hyaline, without fuscous
bands. Abdomen reddish-brown either wholly or with yellow and black marks
on first and second tergites. 7
14a. AGONOCRYPTUS LEUROSUS LEUROSUS, subsp. nov.
Female: Characterized by having the second abdominal tergite less
strongly punctate, more shiny, and abdomen wholly reddish-brown, without
any fuscous or yellow marks. Mesosternum wholly black, without yellow
marks. Fore leg yellow with coxa underneath and femur except dorsally,
black. Fourth and fifth tarsal segments blackish. Middle coxa yellow dor-
sally and black ventrally and on the inner side. Femur yellowish-brown with
black ventral and lateral lines. Trochanters and tibia yellow. Basal two tar-
sal segments yellowish-brown and rest black. Hind coxa, trochanters and
femur reddish-brown. Hind tibia and basal three tarsal segments yellow,
apical two tarsal segments black.
Male: Similar to the female, flagellar segments with long hairs, each
segment also with a long spine-like stout seta among the hairs at the apex of
the segment, particularly segment four onwards. Frons punctate. Pronotum
shiny, with a few striations in the sulcus. Propodeum striato-rugose. Apical
transverse carina of propodeum present.
Black with yellow marks. Abdomen a little brownish apically. Antenna
black, flagellar segments with yellow marks. Head yellow. Apex of mandible,
frons, vertex, and occiput medially black. Pronotal collar, upper part of
pronotum, propleurum, a mark on middle lobe of mesoscutum, scutellum,
metascutellum, tegula, subtegular ridge, a mark behind hind wing, meso-
pleurum broadly, mesosternum wholly, metapleurum except basal region,
and a small T-shaped mark at the apical slope of propodeum, yellow. Coxae
and first trochanters of fore and middle legs yellow. Femora and tibia of both
legs yellowish-brown. Fourth and fifth tarsal segments of fore leg and all tar-
sal segments of middle leg brownish-black. Hind leg black with femur lighter
in color at base. Wings hyaline, a little clouded apically. First tergite yellow,
medially black. Second tergite with an apical yellow band. Third and fourth
tergites basally black and apically yellow. The following tergites yellowish-
brown.
Length: 14-18 mm. Fore wing 10-14 mm.
Holotype: ¢, Brazil: Matto Grosso, Sinap, Oct. 1975, M. Alvarenga
(Townes).
Allotype: %, Brazil: Goias, Jatai, Nov. 1972, F. M. Oliveira (Townes).
Paratypes: 24%, Brazil: Goias, Jatai, 14°, Nov. 1972, F. M. Oliveira
(Townes). Vila Vera, 3%, Oct. 1973, M. Alvarenga (Townes). Vilhena, Rond,
3%, Nov. 1977, M. Alvarenga (Townes).
Distribution: Brazil (map 4).
14b. AGONOCRYPTUS LEUROSUS FLAVOSTERNUM, subsp. nov.
Female: Characterized by having the abdomen reddish-brown as in the
typical subspecies, but the first tergite has a yellow mark at apex, and two
black marks laterally. Second tergite also with a triangular broad apical black
S. Gupta: Genus Agonocryptus (Ichneumonidae) 29
mark. Punctures on second tergite rather strong and more distinct and apical
abdominal tergites more hairy, apical tergite blackish in the middle. Meso-
sternum with yellow marks. Fore leg yellow, coxa with a black ventral mark,
trochanter and femur dorsally blackish-brown, apical tarsal segments brown-
ish. Middle coxa reddish-brown with a yellow triangular spot, trochanters
yellow, femur black dorsally, apical tarsal segments brownish, rest of middle
leg yellowish. Hind coxa, trochanters and femur reddish-brown. Hind tibia
and tarsus yellow with apical two tarsal segments brownish.
Male: Similar to that of leurosus leurosus except that pronotum shiny,
without striations and propodeum striate.
Color similar to that of leurosus leurosus except that yellow mark on meso-
pleurum not extensive and yellow mark on apical slope of propodeum not T-
shaped.
Length: 20mm. Fore wing 16 mm.
Holotype: ¢, Paraguay: Villarica, Dec., F. Schade (Cambridge).
Allotype: %, Paraguay: Carumbe, Feb. 1, 1966, R. Golbach (Townes).
Paratypes: 4°, 140°. Same data as the holotype, 3° (Cambridge).
Carumbe, 1°, March 8, 1966, R. Golbach. Pirareta, 2%, Dec. 26, 1971,
Luis Pena. Bolivia: Altobeni, Palos Blancos, 600 m., 1°, Luis Pena.
Argentina: Salta Pocitos, 3°, Jan. 1972, Manfredo Fritz. Jujuy, Aguas
Calientes, 650m, 2°, Dec. 18-20, 1968, L. Pena. Salta, Tartagal, 1%, Jan.
1972, Fritz (Townes). Argentina: Formosa, Mision-Aishi, 12, Dec. 15, 1948,
R. Solbach. Salta, Campamento Jakulica, 40 kilometers east of Aguas Blancas,
3°, C. Porter. Corrientes Paso de la Patria, 1%, Nov. 5-7, 1969, C. Porter
(Porter).
Distribution: Paraguay, Bolivia, and Argentina {map 4).
15. AGONOCRYPTUS ERUGATUS, n. sp.
Female: Rather stout species. Face finely striate. Clypeus with a few
fine punctures. Malar space aciculate. Frons and vertex smooth and shiny.
Occipital carina close to hypostomal carina, but not touching. Pronotum
minutely punctate, shiny in between. Pronotal sulcus with wrinkles, which
are more prominent in lower half, upper half of groove along hind margin
smooth. Mesoscutum smooth and shiny, only the middle lobe at base with a
few punctures. Scutellum, mesopleurum and metapleurum with a few fine
scattered punctures. Propodeum basad of basal carina smooth and shiny, with
a few scattered punctures, area basad of spiracle with crowded punctures.
Central area of propodeum with rather weak striations with punctures in
between. Striations faded laterally; petiolar area smooth, impunctate. Areolet
about 1.5 as wide as high, with recurrent vein meeting areolet in the middle.
Nervellus intercepted in its upper 0.45. First abdominal segment 2.0 its
apical width. First sternite 0.4 the length of first tergite. All abdominal
tergites shiny, impunctate, sparsely hairy dorsally. Tips of seventh and
eighth with sparse hairs. Ovipositor 0.67 the length of abdomen.
Black with yellow marks; abdomen reddish-brown. Scape ventrally with
two yellow marks. Head yellow. Face with two small marks, two dots along
epistomal groove, margin of clypeus, malar space, mandible except basally,
frons and vertex medially, and upper half of occiput, black. Thorax black
with yellow spots on pronotum dorsally, pronotal collar, upper margin of pro-
notum, propleurum, a triangular mark at apex of middle lobe of mesoscutum,
scutellum, metascutellum, tegula, subtegular ridge, speculum, a mark below
hind wing, long oblong areas on meso- and metapleurum, an elongate mark on
30 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
mesosternum and an inverted T-shaped mark on propodeum, yellow. Fore
and middle legs yellow with their coxae basally black marked, their femora
dorsally brownish-black and apical three tarsal segments brownish-black.
Hind coxa yellow with a large brownish spot basoventrally and along inner side.
Hind trochanters and femur reddish-brown, tibia and tarsus yellow with apical
two tarsal segments dark brown; apex of femur fuscous dorsally. Wings hyaline.
First abdominal segment yellow with a black subapical irregular mark. Second
tergite with a triangular basal yellow mark, an apical yellow stripe, and two
irregular yellow spots on sides, also with two triangular and linear black marks
between the yellow and brownish color of the tergite. Third tergite with an
elongate black basal mark and two yellow spots basolaterally. Apex of abdomen
brownish-black. Intersegmental membranes yellow.
Male: Very slender as compared to the female. Flagellar segments with
long hairs; each segment with a long spine-like seta at its apex, particularly
from fourth flagellar segment onwards. Sculpture generally similar to female
but frons with a few punctures. Pronotum smoother. Propodeum basally with
sparse scattered punctures and a few striations, centrally striate between basal
and apical transverse carinae. Petiolar area of propodeum longitudinally and
irregularly striate (in some males smoother). |
Black with yellow marks. Scape with a small yellow mark. Flagellar
segments 10 to 13 dorsally yellow. Color of thorax similar to that of female
except that black marks on face are absent and yellow mark on propodeum very
small. Fore and middle legs yellow with their femora, tibia and tarsi reddish-
brown. Middle tarsus blackish. Hind coxa yellowish-brown, dorsally with a
dark brown line, femur dark brown, trochanters, tibia and tarsus (except
second and third segments), blackish, second and third segments white, second
often partly blackish. Wings hyaline. First abdominal segment yellow
apically and basally, medially black. Second segment black in basal 0.75.
Third and often the fourth basally black. Rest of tergites reddish-brown with
their bases a little darker.
Length: 8-20 mm; fore wing 5-16 mm.
Holotype: °, Panama: Canal Zone: Margarita, Feb. 1960, S. Breeland
(Townes).
Allotype: %, same locality and collector as the holotype, March 1960
(Townes).
Pavatypes: 4%. Same data as allotype, 2°. Colombia: Rio Atrato
Camp Sautata, 1%, Nov. 11-Dec. 14, 1967. Panama: Barro Colorado Is., 1¢,
March 11-31, 1963, C. & M. Rettenmeyer (Townes).
Distribution: Panama and Colombia (map 4).
V. THE AMOENUS GROUP
This group is characterized by having the frons smooth; face smooth to
finely striate; vertex smooth; occipital carina deflected inwards either strongly
(pointed towards base or middle of hypostomal carina) or weakly (intvicolor), com-
ingvery close to joining hypostomal carina, or erased for a distance equal to the
basal width of mandible; postgenal area somewhat flattened and widened and separ-
ated from the lower portion of gena by a crease (Seeninprofile). Mesoscutum
smooth. Thorax generally smooth. Propodeum striate (except in tricolor).
Apical transverse carina of propodeum absent in females and present in males
(of tvicolor only known). Sometimes transverse carinae at the junction of yellow
and black color prominent and appearing like transverse carina, though not
S. Gupta: Genus Agonocryptus (Ichneumonidae) 31
really present. Abdomen smooth or with scattered minute punctures, particu-
larly on second and third tergites. Petiole long and slender, rounded in cross-
section near its base. Length of first abdominal segment about 3.0 its apical
width (a little shorter in admivandus, about 2.75 x), its sternite long and
extending to 0.70 to 0.8 the length of tergite. Ovipositor about half the length
of abdomen (0. 5-0. 65).
This group includes A. admirandus Cresson from Mexico and three new
species, amoenus and tricolor from Brazil and bispotus from Mexico (Map 5).
A, admirandus can be readily distinguished by having the prepectal carina
short, extending only in the lower 0.5 of mesopleurum; occipital carina
erased for a distance about 0.75 the basal width of mandible; pronotum punc-
tate with area along its hind margin wrinkled, epomia absent, first abdominal
sternite extending to 0.65 the length of tergite, and hind femur largely black.
All other species have the prepectal carina extending up to 0.8 the height of
mesopleurum. A. amoenus is distinctive in having the occipital carina
strongly deflected inwards and coming very close to hypostomal carina near its
base rather than in the apical region; pronotum smooth, epomia absent, groove
along hind margin wrinkled first sternite long, extending to a distance about
0.8 the length of tergite, abdominal tergites without hairs. Hind femur with
extensive blackish marks. In all other species of this group the apical abdom-
inal tergites are beset with conspicuous hairs.
A. bispotus is the only species of this group with epomia. It has the
occipital carina deflected inwards but is erased for a distance equal to the
basal width of mandible, pronotum punctate in the middle groove and striate
along hind margin, first sternite about 0.75 the length of its tergite, hind femur
largely yellow, and the speculum yellow (as is the case in admivandus, while in
other species it is black). A. tricolor is the only species in which the propode-
um is smoother in the female, with only a few trans-striations centrally. In
male the propodeum is striate and the apical transverse carina is distinct. It
has the occipital carina erased as in bispotus, but not deflected inwards, pro-
notum with minute scattered punctures, groove along hind margin smooth,
epomia absent, first sternite extending up to 0.75 the length of its tergite,
and hind femur red.
The males have the occipital carina a little closer to the hypostomal carina
and the hind leg largely black. They also have large hairs on the antennal
flagellum. White marks on flagellar segments are present dorsally or absent,
but not forming a complete ring.
16. AGONOCRYPTUS ADMIRANDUS (Cresson)
Mesostenus (Mesostenus) admirandus Cresson, 1873, Proc. Acad. Nat.
Sci. Philadelphia, 1873: 155. %. key, des. Type: ¢, Mexico: Orizaba
(Philadelphia).
Agonocryptus admivandus: Townes, 1946, Bol. Ent. Venezolana, 5: 31.
Townes, 1966. Mem. Amer. Ent. Inst. 8: 128.
Female: Face and clypeus shiny with a few fine striations. Frons shiny
with a few fine punctures close to ocelli. Vertex medially with a few super-
ficial punctures. Malar space granulose, equal to the basal width of mandible.
Temple smooth and shiny, a little granulose close to malar space. Occipital
carina erased for a distance about 0.75 the basal width of mandible. Meso-
scutum shiny, with scattered punctures. Pronotum with scattered punctures.
Pronotal sulcus with a few striations. Scutellum punctate. Mesopleurum and
32 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
metapleurum shiny and with scattered superficial fine punctures. Mesopleurum
just below subtegular ridge striate. Prepectal carina reaching 0.5 the height
of mesopleurum. Propodeum basally between the two yellow marks semicircu-
larly striate, punctate basolaterally just above the spiracle; centrally punctato-
striate. Petiolar area of propodeum laterally punctate, in the middle shiny and
with a few trans-striations. Areolet pentagonal, wider than high. Second
recurrent vein meeting areolet at its middle. Nervellus intercepted at its
upper 0.33. First abdominal segment slender, nearly 2.75 x its apical
width, impunctate. First sternite extending up to 0.7 its length. Second
abdominal tergite with fine scattered superficial punctures medially and sub-
medially. Third tergite basally finely and closely punctate. The following ter-
gites finely mat. Ovipositor about 0.65 the length of abdomen.
Black with yellow marks and bands. Head (including face) yellow except
frons, vertex and occiput medially, malar space, clypeal margin and apex of
mandible, black. The following parts are yellow: A mark on pronotal collar,
upper part of pronotum, propleurum apically, a central mark on mesoscutum,
scutellum and metascutellum wholly, tegula, subtegular ridge, speculum, a
mark below wings, mesopleurum, metapleurum and mesosternum broadly, two
squarish marks at base of propodeum, and a dagger-shaped mark at the apical
area of propodeum (this mark reaching up to basal transverse carina). Fore
and middle legs yellow, except coxa, trochanters and femur dorsally with
black line, their tarsi brownish. Hind coxa yellow with two lateral longitudinal
black lines. Hind trochanters and femur black with a yellow longitudinal ven-
tral line, third tibia and tarsus yellow. Wings hyaline, first abdominal tergite
yellow with a subapical black mark. Second tergite with a triangular yellow
basal mark, its sides with yellow marks connected to the apical transverse
yellow band. All other abdominal tergites with yellow apical bands, their
sides also yellow. Seventh and eighth tergites broadly yellow laterally, with
the eighth tergite black up to the apex.
Male: Unknown.
Length: 18mm; fore wing 12 mm.
Specimen examined: Mexico: 1 (type) (Philadelphia).
The locality label on specimen does not state precise type-locality.
Distribution: Mexico (map 5) .
17. AGONOCRYPTUS AMOENUS, n. sp.
Female: Face and clypeus shiny, impunctate with face finely trans-
striate in the middle. Malar space granulose. Frons and vertex shiny, impunc-
tate. Temples smooth and shiny. Pronotum shiny, impunctate. Epomia
absent. Mesoscutum shiny, impunctate. Mesopleurum and metapleurum shiny
with a few scattered fine and superficial punctures. Prepectal carina 0.8 the
height of mesopleurum. Propodeum finely distinctly striate, striations
arched and areas in between shiny. Area basad of basal carina semicircularly
striate, particularly in the central basal area. Areolet pentagonal, wider
than high. Second recurrent vein meeting areolet at its apical 0.4. Nervellus
intercepted at its upper 0.33. Abdomen wholly smooth and shiny, without
punctures. First abdominal segment 3.0 its apical width and slender, its
sternite reaching up to 0.175 the length of its tergite, ovipositor about 5.3 x
the length of abdomen.
Black with yellow marks and bands. Head (including face) yellow with
apex of mandible, with frons, vertex, and occiput medially, black. Pronotal
collar near neck and upper margin of pronotum yellow. A central mark on
S. Gupta: Genus Agonocryptus (Ichneumonidae) 33
mesoscutum, scutellum, metascutellum, tegula, subtegular ridge, a mark
below wings, mesopleurum broadly, mesosternum wholly, upper 0.75 of meta-
pleurum, two rectangular marks at base of propodeum and a dagger-shaped
mark at the apical area of propodeum, yellow speculum black. Fore leg with
coxa, trochanters, and femur yellow with femur dorsally darker, its tibia and
tarsus yellowish brown. Middle leg with coxa, first trochanteral segment and
femur yellow, with coxa marked black ventrally and femur dorsally. Second
trochanteral segment black and tibia and tarsus brown. Hind leg with coxa
yellow with a dorsal black line, its trochanters black, basal 0.5 of femur and
0.25 of tibia yellow. Hind tarsus yellow. Wings hyaline.
Male: Unknown.
Length: °, 18mm. Fore wing 12 mm; ovipositor 0.55 as long as abdomen.
Holotype: ¢, Brazil: Matto Grosso, Sinop, 12° 31'S, 55° W,Oct. 1975,
M. Alvarenga (Townes).
Distribution: Brazil (map 5).
18. AGONOCRYPTUS BISPOTUS, n. sp.
Female: Face and clypeus shiny, impunctate, area just below antennal
socket with a few striations. Malar space granulose. Frons and vertex
shiny, impunctate. Occipital carina erased for a distance equal to the basal
width of mandible. Pronotum with scattered fine punctures (especially in the
sulcus). Pronotal collar impunctate. Epomia present. Mesoscutum smooth
and shiny, impunctate. Scutellum, mesopleurum and metapleurum mostly
shiny, with a few fine punctures. Prepectal carina 0.8 the height of meso-
pleurum. Propodeum trans-striate, striations not very close, interspaces
with punctures. Area basad of basal carina with weak striations. Striations
in the petiolar area rather strong. Areolet wider than high. Second recurrent
vein meeting areolet in its apical 0.33. Nervellus intercepted at its apical
0.33. First abdominal segment slender, nearly 3.0 its apical width, its
sternite extending up to 0.75 the length of its tergite. First abdominal tergite
shiny, impunctate. Second tergite medially finely punctate. Third also finely
punctate. The following tergites smooth. Ovipositor about 0.5 the length of
abdomen.
Black with yellow marks and bands. Head yellow except frons, vertex
and occiput medially and apex of mandibles black. Pronotum along its collar
and upper margin broadly, propleurum except basally, a rectangular mark on
mesoscutum, scutellum, metascutellum, tegula, subtegular ridge, speculum,
a mark below wings, mesopleurum, mesosternum and metapleurum broadly,
two squarish marks at base of propodeum and a dagger-shaped mark at apical
slope of propodeum, yellow. Legs yellow, except all coxae dorsally black
marked. Hind trochanters black. Hind femur and tibia apically darker. Hind
tarsus whitish-yellow. Fore and middle trochanters and femur dorsally
darker. Wings hyaline. First abdominal tergite with a sub-basal bifurcated
mark. All abdominal tergites except the eighth, with yellow apical bands.
Second and third tergites with sub-basal lateral spots. Sides of third to
seventh tergites yellow. Eighth tergite wholly black.
Male: Unknown.
Length: 18 mm; fore wing 12 mm.
Holotype: 2, Mexico: Oaxaca, Metate, 85.5 kilometers south of Tuxtepec,
900 m, Oct. 16, 1962, H. & M. Townes (Townes).
Distribution: Mexico (map 5).
34 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
19. AGONOCRYPTUS TRICOLOR, n. sp.
Female: Face and clypeus shiny. Face submedially, below antennal
socket with a few striations. Clypeus with a few fine striations laterally.
Malar space granulose, equal to the basal width of mandible. Frons and ver-
tex smooth and shiny. Occipital carina erased for a distance, away from the
hypostomal carina (as in bispotus), but this carina not deflected inwards; this
area appears rough. Pronotum with minute scattered punctures, its hind mar-
gin smooth. Epomia absent. Mesoscutum shiny, impunctate. Scutellum,
mesopleurum and metapleurum shiny and with a few scattered punctures.
Prepectal carina 0.8 the height of mesopleurum. Propodeum smooth with
area apicad of basal transverse carina with weak striations interposed with
shallow punctures. (Sides of propodeum smooth, and whole propodeum much
more shiny than in other species of this group.) Areolet much wider than high.
Second recurrent vein meeting areolet at its middle. Nervellus intercepted at
its upper 0.33. First abdominal segment smooth and shiny, slender, 3.0 its
apical width, its sternite extending to 0.75 the length of its tergite. Second
tergite with minute scattered punctures sub-basally. Third tergite finely
punctate. The following tergites smooth and shiny. Ovipositor about 0.6 the
length of abdomen.
Black, marked with yellow. Abdomen reddish-brown. Head yellow except
frons, vertex and occiput medially, malar space and apex of mandible, black.
A rectangular mark on mesoscutum, two marks on pronotal collar, upper edge
of pronotum, propleurum apically, scutellum, metascutellum, tegula, sub-
tegular ridge, an oblong (somewhat L-shaped) mark on mesopleurum, a mark
on mesosternum, an oblong mark on metapleurum, two oval marks on basal
area of propodeum, and a dagger-shaped mark on apical slope of propodeum,
yellow. Speculum black. Fore and middle legs yellow except their coxae,
trochanters and femora dorsally black. Hind coxa, trochanters, and femur
reddish-brown with coxa dorsally with a yellow oval mark and a black line on
its outer side. Hind tibia and tarsus yellowish, with last tarsal segment
black. Wings hyaline. First tergite yellow basally and apically, medially
black. The rest of the tergites reddish-brown with tip of abdomen black.
Male: Generally similar to the female. Flagellar segments with long
hairs. Each segment also with long spine-like stout seta amongst the hairs
at the apex of the segment, particularly from fourth onwards. Frons punctate.
Pronotum shiny, Propodeum centrally with strong striations. Apical trans-
verse carina present.
Color black with yellow marks. Antenna black, without yellow mark
dorsally. Head yellow. Apex of mandible, frons, vertex and occiput medially
black. Pronotal collar, pronotum, propleurum, a mark on middle lobe of
mesoscutum, scutellum, metascutellum, tegula, subtegular ridge, speculum, a
mark behind hind wing, mesopleurum broadly, mesosternum wholly, meta-
pleurum except basal region, and petiolar area of propodeum, yellow. Fore
and middle coxae and first trochanters yellow, their femora and tibiae yellowish-
brown. Fore tarsus basally yellow, apically black. Middle tarsus black.
Hind coxa black, apically yellow, their trochanters, femur, tibia and tarsus
black. Hind femur lighter in color basally. Wings hyaline, apically a little
fuscous. Abdomen black, with first tergite basally and apically, and the
following tergites apically and apicolaterally yellowish-brown.
Length: 10-18 mm. Fore wing 10-14 mm.
Holotype: 2, Brazil: Matto Grosso, Sinop, 12° 31'S. 55° 37' w.,
Oct. 1975, M. Alvarenga (Townes).
S. Gupta: Genus Agonocryptus (Ichneumonidae) oa
Allotype: &, same data as the type (Townes).
Pavratypes: 27%, same data as the type, collected October 1974, 75, and
1976 (Townes).
Distribution: Brazil (map 5).
VI. THE RUGIFRONS GROUP
The Rugifrons Group is characterized by having the frons rugose; face
trans-striate to somewhat rugoso-striate; vertex punctate or sparsely so;
whole of thorax including propodeum strongly punctate; and whole of abdomen
punctate. In males the first tergite is smoother or more sparsely punctate
and thorax also somewhat less strongly punctate.
This group includes A. rugifrons with clear wings, reddish abdomen
and body with yellow marks; A. mulleus, with clear wings, and body wholly
reddish-brown; and A. fumosus and A. infuscatus with blackish-brown wings,
reddish thorax and black abdomen. They occur in Argentina and Brazil.
20. AGONOCRYPTUS RUGIFRONS, n. sp.
Male and Female: Face trans-striate with punctures in between. Face
centrally strongly rugose. Clypeus granulose, with scattered punctures, its
apical margin with a minute median tooth. Malar space as long as the basal
width of mandible, granulose. Temple smooth and shiny. Frons rugose.
Vertex punctate. Occipital carina incurved and meeting hypostomal carina.
Pronotum punctate, its sulcus trans-striate. Epomia absent. Mesoscutum
closely and deeply punctate. Scutellum sparsely, superficially punctate.
Mesopleurum, metapleurum, and propodeum wholly strongly punctato-rugose.
Apical transverse carina of propodeum interrupted medially. Areolet rectangu-
lar, about 1.4 as wide as high. Second recurrent vein meeting areolet distad
of its middle. Nervellus intercepted about the middle. First tergite less than
2.0 its apical width, its sternite ending at the level of spiracle, about 0.5 the
length of its tergite. All tergites punctate. First tergite closely and deeply
punctate medially. Second and third tergites mat and with compact deep punc-
tures. The following tergites with finer punctures and finely mat. Ovipositor
equal to the length of abdomen.
Black with yellow marks. Abdomen reddish-brown to blackish-brown.
Head black, except for basal half of clypeus, labrum, and a broad interrupted
orbital ring. A mark on mesoscutum, scutellum, metascutellum, interrupted
pronotal collar, upper part of pronotum, tegula, subtegular ridge, speculum,
a small mark on apical corner of mesopleurum, a mark below wings, an
elongate mark on dorsal part of metapleurum, and an inverted T-shaped mark
on petiolar area of propodeum (which does not reach the basal transverse
carina), whitish-yellow. Wings hyaline. Legs reddish-brown, with fore coxa
and first trochanter dorsally and hind tarsal segment yellowish-white. Abdo-
men largely brown. First tergite apically with a broad white band. The follow-
ing tergites with a narrow white band. Color of abdominal tergites variable
from reddish-brown to blackish brown.
Length: 16mm. Wings 10 mm.
Holotype: 2, Argentina: Jujuy, Jan. 16, 1966, H. & M. Townes (Townes).
Allotype: ©, same data as the type (Townes).
Parvatypes: 32°, 33°, Argentina: from Horco Molle (near Tucuman),
Calalao, San Pedro de Tucuman, Jujuy, El Pintado, Al Tola Vina, Salta,
36 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
Yacochuya (Tafayata), Tacuil, Angastaco, San Miguel de Tucuman, Amaicha
del Valle, Aguas Blancas, Trances Tacanas, and Arnau. Collected on various
dates during January, February, March, April, September, October, Novem-
ber, and December (Townes, Cambridge and Ottawa).
Distribution: Various localities near Tucuman, Argentina (map 6).
21. AGONOCRYPTUS MULLEUS, n. sp.
Female: Face rugose. Clypeus rough, with a few striations apicolater-
ally, its margin with a median apical tooth. Malar space aciculate, 0.8 as
long as the basal width of mandible. Temple shiny, with a few superficial
punctures close to malar space. Frons rugose. Vertex punctate medially,
punctures not deep. Occipital carina not meeting hypostomal carina. Pronotum
deeply and closely punctate, punctures running into striations along the sulcus
and along hind margin. Epomia absent. Mesoscutum and scutellum closely
and deeply punctate, appearing rugose at places. Mesopleurum, metapleurum
and propodeum wholly strongly punctato-rugose. Apical transverse carina of
propodeum broadly interrupted medially. Areolet pentagonal, about 1.4 as
wide as high. Second recurrent vein meeting areolet at its apical 0.4. Second
intercubitus unpigmented. Nervellus intercepted at its upper 0.4. First ter-
gite not stout, 2.0 as long as its apical width. First sternite ending at the
level of spiracle, about 0.5 as long as the tergite. First tergite shiny, witha
few scattered punctures medially. Second and third tergites finely, closely
punctate. The following tergites finely mat. Ovipositor 0.5 as long as the
abdomen.
Reddish-brown. Scape and basal flagellar segments reddish-brown.
Narrow (interrupted) inner and outer orbital rings, labrum, pronotal collar
and propleurum centrally, and tegula, white. Wings hyaline. Basal tarsal
segments of middle and hind legs white. Apical tarsal segments blackish.
Length: 15mm. Fore wing 10 mm.
Male: Unknown.
Holotype: 2, Argentina: Misiones, Leandro N. Alem., Inst. Alberdi,
Nov. 17-19, 1969, C. Porter (Porter).
Distribution: Argentina (map 6).
22. AGONOCRYPTUS INFUSCATUS, n. sp.
Female: Face and clypeus transversely striate, with punctures in
between. Clypeal margin with a median minute tooth. Malar space strongly
granulose, as long as the basal width of mandible. Temple smooth and shiny,
near malar space finely striate. Frons rugose. Vertex sparsely punctate,
punctures rather shallow. Occipital carina not meeting hypostomal carina.
Pronotum deeply and closely punctate. Pronotal sulcus without any striations.
Epomia absent. Mesoscutum and scutellum closely punctate. Mesopleurum
punctate. Area below subtegular ridge a little striate. Speculum shiny, with
fine scattered punctures. Metapleurum punctate to striato-punctate. Basal
area of propodeum sparsely punctate. Apical transverse carina present only
on sides. Area between basal and apical transverse carinae striato-punctate.
Petiolar area shiny, with a few longitudinal striations. Areolet rectangular,
1.5 as wide as high. Second recurrent vein meeting areolet at its apical 0.3.
Nervellus intercepted above its middle. Petiole stout, nearly 2.0 as long as
its apical width. First sternite reaching spiracle. Abdominal tergites punc-
tate. First tergite punctate strongly on apical half. Second, third and fourth
S. Gupta: Genus Agonocryptus (Ichneumonidae) 37
tergites closely punctate. The following tergites mat. Ovipositor 0.7 as long
as the abdomen, its tip pointed, narrow and tapering, with seven teeth.
Reddish-brown with black abdomen. Head reddish-brown. Face reddish-
brown, without yellow orbital stripes. Malar space and mandibles black.
Wings strongly infuscate. Legs black except coxae. Fore femur ventrally
and tibia dorsally, brownish. Hind femur black. Second and third hind tarsal
segments yellow. Abdomen black with only the first tergite basally brown.
Length: 18mm. Fore wing 12 mm.
Male: Unknown.
Holotype: °, Brazil: Nova Teutonia, Santa Catarina, Oct. 1970,
F. Plaumann (Townes).
Paratype: °, same data as the holotype, but Nov. 1970 (Townes).
Distribution: Brazil (map 6).
This species is rather close to A. rufithovax in general appearance, but
can be differentiated by the structure of frons, first tergite, nature of oviposi-
tor teeth, absence of apical transverse carina of propodeum, and also by the
color of malar space, orbital rings, hind tarsus and wings.
23. AGONOCRYPTUS FUMOSUS, n. sp.
Female: Face finely transversely striate, with a few rugosities in the
middle. Clypeus finely striate, its apical margin with a median tooth. Malar
space granulose, with a few longitudinal striations, about as long as the basal
width of mandible. Temple similar to that of infuscatus. Frons rugose.
Vertex closely and finely punctate. Occipital carina meeting hypostomal cari-
na. Epomia absent. Pronotum punctate. Pronotal sulcus punctato-striate.
Mesoscutum closely and deeply punctate. Scutellum sparsely punctate. Meso-
pleurum finely and closely punctate, area below subtegular ridge punctato-
striate. Metapleurum deeply and closely punctate. Apical transverse carina
of propodeum absent or merged into striations on propodeum. Propodeum
punctato-striate. Petiolar area smooth and with a few longitudinal ridges.
Wings and abdomen as in A. infuscatus. Ovipositor tip blunt, not tapering, and
with only 5 teeth. Ovipositor 0.6 as long as the abdomen.
Reddish-brown with head and abdomen black. Face black, with yellow.
Interrupted orbital rings. Wings infuscate. Fore leg black with femur ven-
trally and tibia yellowish-brown. Middle coxa reddish-brown, trochanters
black, and rest of middle leg brownish. Hind coxa and femur reddish-brown;
trochanters, femur apically, tibia, basal half of basitarsus, and fifth tarsal
seement, black. Hind tarsus otherwise yellow. Abdomen black, with first
tergite reddish-brown.
Male: Rather similar to the female, with pronotal groove smoother,
fore leg lighter in color and abdomen brown rather than black.
Length: ?, 18mm. Fore wing 12mm. Male 13mm. Fore wing 8-10
mm.
Holotype: ¢, Brazil: Nova Teutonia, Santa Catarina, April 14, 1952,
F. Plaumann (Townes).
Allotype: %, Argentina: La Plata, Dec. 18, 1965, H. & M. Townes
(Townes).
Pavatypes: 4°, 3°. Argentina: La Plata, 1°, Dec. 18, 1965, H. & M.
Townes (Townes). Berisso, 1°, Dec. 8, 1965, H. & M. Townes. Mar del
Plata, Prov. Buenos Aires, 19, Nov. 1, 1949 (Townes). Buenos Aires, Abra
de la Ventana, 12, Feb. 6, 1947 (Porter). Brazil: Nova Teutonia, Santa
Catarina, 1°, Nov. 11, 1952, 1°, Nov. 1955, F. Plaumann (Townes); 18,
38 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
April 26, 1960 (Porter).
Distribution: Brazil and Argentina (map 6).
Acknowledgments: I am grateful to Dr. Henry Townes for giving me the
opportunity to study at the American Entomological Institute and for his gui-
dance and assistance at every stage of the investigation. I am also thankful
to the curators of the various museums from where the types and other collec-
tions were borrowed for the present study. The respective locations of the
types and other material received for study are given in the text after the
specimens examined.
REFERENCES
Brues, Charles T. 1912. Brazilian Ichneumonidae and Braconidae Obtained
by the Stanford Expedition. Ann. Ent. Soc. America 5(3): 193-228.
Brulle, M. A. 1846. In Lepeletier: Histoire Naturelle des Insects.
Hymenopteres 4: 1-680.
Carlson, R. W. 1979. Family Ichneumonidae. Jn Krombein ef al.: Catalog
of Hymenoptera in America North of Mexico. 1: 315-741.
Cresson, E. T. 1873. Description of Mexican Ichneumonidae. Proc. Acad.
Nat. Sci. Philadelphia 1873: 104-176.
Cushman, R. A. 1929. A Revision of the North American Ichneumon-flies of
the genus Mesostenus and Related Genera. Proc. U. S. Natl. Mus.
74(16): 1-58.
Taschenberg, E. L. 1876. Einige neue tropische, namentlich Stidamerika-
nische. Ztschr. f. die Gesam. Naturw. Halle 48: 61-104.
Townes, Henry K. 1946. The Generic Position of Neotropic Ichneumonidae
(Hymenoptera) with Types in the Philadelphia and Quebec Museums,
Described by Cresson, Hooker, Norton, Provancher and Viereck.
Bol. Ent. Venezolana 5: 29-63.
Townes, Henry K. & Marjorie 1962. Ichneumon-flies of America north of
Mexico 3: subfamily Gelinae, Tribe Mesostenini, U. S. Natl. Mus. Bull.
216(3): 1-602.
Townes, Henry & Marjorie 1966. A Catalogue and Reclassification of Neo-
tropic Ichneumonidae. Mem. Amer. Ent. Inst. 8: 1-367.
Viereck, H. L. 1905. Notes and Descriptions of Hymenoptera from the
Western United States in the Collection of the Univ. of Kansas. Trans.
Kansas Academy Sci. 19: 264-326.
39
SOplOT eploosip
(SOUMO] PUB SOUMO], 19378)
SsnosuTyotyo SA. LUAUOONODV ‘I ‘31d
cat ee RAAT
40 Contrib. Amer. Ent. Inst. , vol. 19, No. 2, 1982
4A. chichimecus'
chichimecus
e A.chichimecus
discoidaloides
e A.ruficrus
x* A. bicolor
Map 1. AGONOCRYPTUS - Chichimecus Group
S. Gupta: Genus Agonocryptus (Ichneumonidae) 4]
* A. rufithorax (Chichimecus Gr.)
» A. russulus ( nn )
Oo A. heathi (Heathi Group )
a A. violasceng (Group ?)
Map 2. AGONOCRYPTUS - Chichimecus Group, Heathi Group
42 Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
a A. lioneli lioneli
A A. lioneli cake
e A. argentinus argentinus
xy A. argentinus tucumanus
A. physocnemis physocnemis
© A. physocnemis nigristernum
Map. 3. AGONOCRYPTUS - Physocnemis Group
S. Gupta: Genus Agonocryptus (Ichneumonidae) 43
. gossypii
. erugatus
A
A
* A. rufigaster
A. adustus adustus
A
. adustus paulus
«CSE
- varus varus
S
Pass 3 nee
Se
Ps:
ow
A
A. varus nigrifemur
4 A. leurosus flavosternum
A
. leurosus leurosus
Map. 4. AGONOCRYPTUS - Varus Group
Contrib. Amer. Ent. Inst., vol. 19, no. 2, 1982
44
ems ems eee, ween wm wi i ie ii me ee ww me fle ae me me mee -_ Se yaa ei ce ae re Poa ol ke dies” JZ
So
JO[OOII}] We snusowe
&yQ G bee
dnoiy snuso0owy - SNLHAYDONODYV ‘co dey
S. Gupta: Genus Agonocryptus (Ichneumonidae)
rugifrons
4 A. fumosus
# A. mulleus
© A. infuscatus
Map 6. AGONOCRYPTUS - Rugifrons Group
45
ees
ee
3
:
5
ie
ipa
$id
eure:
A REVIEW OF THE GENUS CRYPTOHELCOSTIZUS
(HYMENOPTERA: ICHNEUMONIDAE)
by
Santosh Gupta *
American Entomological Institute
5950 Warren Road, Ann Arbor, Michigan 48105
The genus Cryptohelcosti zus was described by Cushman (1919) with
C. rufigaster (from California) as the type-species. In 1922, he synonymized
rufigaster with Cryptus alamedensis Ashmead (1890). Viereck (1921) described
C. dichrous from North Carolina. Cushman (1940) added two more species:
C. chrysobothridis and C. ornatus from Oklahoma and California, respectively.
Townes and Townes (1962) added six more species: genalis, leiomerus,
caudatus and maculosus from California, and fumipennis and nigricans from
Arizona. Thus a total of ten species are at present known under the genus,
all from the U.S.A., in the Nearctic Region.
In the Townes Collection there were a number of unstudied specimens
from Northwestern United States, which prompted me to make a restudy of
the genus. All the types were kindly loaned to me by the curators of the
various museums. No new species turned up in the collections, but a new
subspecies of C. genalis is described from Oregon. New distributional
records are given for the various species, and a key is provided to distinguish
them. In the treatment that follows, only the significant characters of the
species are mentioned, and the records of specimens studied. For fuller
descriptions refer to Townes and Townes (1962). Synonymical references to
the species can be seen in the catalogues of Townes (1944), Townes and Townes
(1951) and Carlson (1979).
The genus Cryptohelcostizus has been traditionally put under the old sub-
family Cryptinae close to Helcostizus Foerster and Xylophrurus Foerster.
Townes and Townes (1962) placed it under the subtribe Echthrina of tribe
Mesostenini, subfamily Gelinae. In 1970, Townes chanted the name of the
subtribe to Gabuniina. With the raising of the tribe Mesostenini to subfamily
Mesosteninae by Gupta (1970), the Gabuniina becomes the tribe Gabuniini.
Genus CRYPTOHELCOSTIZUS Cushman (fig. 1)
Cryptohelcostizus Cushman, 1919. Proc. U. S. Natl. Mus., 55: 534.
Type-species: (Cryptohelcostizus rufigaster Cushman) = alamedensis
(Ashmead); original designation.
Taxonomy: Townes and Townes, 1962: 504. Carlson, 1979: 478.
The salient features of the genus are: Head transverse. Clypeus short,
convex, its apical margin broadly truncate, without a median tooth. Sternaulus
absent. Pleural carina and apical transverse carina of propodeum absent.
Propodeum usually short and rugoso-punctate. Basal transverse carina always
present. Areolet pentagonal, large, 0.5 to 0.9 as high as second recurrent
* Present address: Center for Parasitic Hymenoptera. Dept.
of Entomology & Nematology, Univ. of Florida, Gainesville, FL 326ll.
2 Contrib. Amer. Ent. Inst., vol. 19, no. 3, 1982
vein. Nervulus basad of basal vein. Nervellus intercepted below its middle.
Fore femur in female concave below. First tergite without a lateral triangular
tooth at base, its dorsolateral carina weak or absent, ventrolateral carina
present. Ovipositor 0.5 to 1.0 the fore wing length.
Distribution: Nearctic Region.
Host: Buprestid larvae boring in branches and twigs of trees and shrubs.
Two species groups can be recognized based on the nature of the basal
transverse carina of the propodeum and the coloration of the wings:
I. The Alamedensis Group, characterized by having the wings clear
hyaline, and the basal transverse carina of propodeum complete, uniformly
arched or sometimes narrowly interrupted medially, but never turned basad
medially. This group includes C. alamedensis, nigricans, maculosus, ornatus,
caudatus, and chrysobothridis.,
Il. The Dichrous Group, characterized by having the wings black or strongly
infuscate, and basal transverse carina of propodeum interrupted medially and
each end turned basad. This group includes C. dichrous, genalis, fumipennis,
and leiomerus.
KEY TO THE SPECIES OF CRYPTOHELCOSTIZ US
1. Wings clear hyaline. Basal transverse carina of propodeum complete,
uniformly arched or sometimes narrowly interrupted medially, but
never turned basad in the middle (Alamedensis Group)........ 2
Wings black or strongly infuscate. Basal transverse carina of propodeum
interrupted medially and its ends turned basad medially (Dichrous
POUR ce a Se NE ee sii ees Lae owes ee 6 abe 7
2. Hind femur on its front side with very sparse hairs, their sockets separated
by more thang. 0 the lengli of baire. 00s wor) a.telen aia 3
Hind femur on its front side with closely set hairs, their sockets
separated by 0.7 to 2.0 x the length of hairs. .... 6 45. So.ha ne 6
3. Hind femur polished, black. Nervulus basad of basal vein by 0.5 to 0.66
its length (by more than half its length). Propodeum dorsally flat, not
very convex. Trochanters of fore leg black ventrally.
2. nigricans Townes and Townes (p. 4)
Hind femur granulose, subpolished. Nervulus basad of basal vein by less
than half its length. Propodeum dorsally convex, sloping. Trochanters
of fore leg with white marks ventrally sa BO RIS oo se 4
4. Basal transverse carina of propodeum complete and uniformly arched.
Propodeum and hind coxa black, without any spot or mark.
1. alamedensis (Ashmead) (p. 4)
Basal transverse carina of propodeum narrowly interrupted medially with
the ends not turned basad medially. Propodeum and hind coxa with
VOROM CRATE: BVO RAS RR kG ea BU DN eli s gala aren gy at 9)
0. Mesopleurum and metapleurum each with a large yellow mark. Vertex
deeply and closely punctate. Second intercubitus weak medially.
3. maculosus Townes and Townes (p. 5)
S. Gupta: Genus Cryptohelcostizus (Ichneumonidae) 3
Mesopleurum and metapleurum without any yellow marks. Vertex with
sparse, moderate sized punctures. Second intercubitus uniformly
strong. (Ovipositor sheath 0.4 the length of front wing.)
4. ornatus Cushman (p. 5)
Propodeum and hind coxa marked with white. Ovipositor sheath 0.75 the
length of front wing. Legs lighter in color.
5. caudatus Townes and Townes (p. 6)
Propodeum and hind coxa black, without any white marks. Ovipositor
sheath 0.4 the length of front wing. Legs darker in color.
6. chrysobothridis Cushman (p. 6)
Hairs on front face of hind femur moderately dense, their sockets
separated by about 0.7 the length of the hairs. Punctures on meso-
pleurum separated by about 0.7 their diameter. Prepectal carina
reaching subtegular ridge. Face granulose, with punctures on sides
and rugulose medially. Pronotal collar black without any central
white oe Dro wit Marks) ws Wowie sé i 7. dichrous Viereck (p. 7)
Hairs on front face of hind femur sparser, their sockets separated by 2.0
the length of the hairs. Punctures on mesopleurum separated by about
0.4 their diameter. Face shiny with punctures or with a few oblique
striations. Pronotal collar with a white or brown mark medially
(except in leiomerus). Prepectal carina usually reaching 0.6 to 0.75
Tie heir WET BaDOIeN TENT: SUT i, ae ae Se ie se ee ae, x8 8
Hind margin of temple, and its occipital carina, strongly bulging outward
at the lower corner of the eye. Face strongly punctate. Vertex
moderately closely punctate close to ocelli.
| 8. genalis Townes and Townes 9
Hind margin of temple, and its occipital carina, not bulging outward, some-
times a little convex. Side of face punctate. Vertex sparsely punctate
C1LOGO.T0 Geen PT ricwteec's SRC ee en 10
Hind femur reddish-brown. Coxa brownish-black. Propodeum ruguloso-
punctate. First tergite shiny and grooved subapically.
8a. genalis genalis Townes and Townes (p. 7)
Hind coxa and femur black. Propodeum punctato-striate. First tergite
punctate and not grooved. . 8b. genalis niger, new subspecies (p. 8)
First tergite sparsely and finely punctate. Clypeus and upper part of pro-
notum marked with white. Temple weakly convex. Second abscissa of
cubitus about 1.4 as long as the third abscissa.
9. leiomerus Townes and Townes (p. 8)
First tergite moderately punctate dorsally. Clypeus and upper part of pro-
podeum marked with white. Temple moderately convex. Second
abscissa of cubitus about 1.15 as long as the third abscissa.
10. fumipennis Townes and Townes (p. 9)
4 Contrib. Amer. Ent. Inst., vol. 19, no. 3, 1982
I. THE ALAMEDENSIS GROUP
1. CRYPTOHELCOSTIZUS ALAMEDENSIS (Ashmead)
Cryptus alamedensis Ashmead, 1890. Proc. U. S. Natl. Mus., 12: 409.
2. Type: ¢, Alameda, California (Washington).
Cryptohelcostizus rufigaster Cushman, 1919. Proc. U. S. Natl. Mus.,
55: 534. oO, 9. Type: 2, Harold, California (Washington).
The characteristic features of this species are: Mesopleurum with fine
rugosities. Propodeum dorsally convex and sloping. Basal transverse carina
of propodeum complete and evenly arched. Nervulus basad of basal vein by
less than 0.5 its length. Hind femur granulose with very sparse hairs. Ovi-
positor 0.9 as long as fore wing. Ovipositor sheath about 0.65 as long as fore
wing.
Black with reddish abdomen. A mark onclypeus, base of mandible, a mark
on pronotum, a narrow interrupted orbital mark and metascutellum, white.
Propodeum black, sometimes with two very small marks on apical area.
Wings hyaline. Legs brownish. First trochanter of fore leg white ventrally.
Hind coxa black. Basal 0.5 of first abdominal tergite brownish-black.
Specimens: 619, 260%. U.S. A.: California: Leevining, 4%, June 22,
1948. Portero in San Diego Co., 119, 50, April 8-17, 1974. Lake Wohford,
San Diego Co., 119, 1%, April 21-May 1, 1974. Julian, 242, 10°, May 6-30,
1974. North of Leggett, 1°, May 18, 1978 (All above collected by H. and M.
Townes and in Townes Collection.). California: Simla Station, %, June 28,
1922, R. D. Hartman, on Apricot, parasitic on Chrysobothris mali. Los
Gatos, 1%, May 23, 1918, R. D. Hartman, on Osmaronia, parasitic on
Chrysobothris mali. Walter Sqr., Napa Co., 12, May 26, 1951, E. I.
Schlinger (Townes). Elk Grove, Sacramento Co., 1%, Sept. 24, 1949, H. A.
Hunt (Townes). W. Walker R., 6000 ft., 2, C. D. Michner, on Prunus
(Townes). Idaho: near Stanley, 6000 ft., 2, Aug. 8, 1978 (Townes). Low-
man, 6000 ft., 2, April 14, 1978, H. & M. Townes (Townes). Nevada:
Tuscarora, “, June 5, 1978, H. & M. Townes (Townes). Oregon: Selma, 22,
30°, May 20-21, 1974, H. & M. Townes (Townes). Hyatt Reservoir, 3%, May
2, 20, and 22, 1974, H. & M. Townes (Townes). Pinehurst, 3¢, June 23 and
29, 1974, H. & M. Townes (Townes). Utah: Strawberry Daniel Pass, ¢, June
19, 1948, H., M., G. & D. Townes (Townes).
Variations: Two females from California: Poterero, April 8, 14, 1974 are
lighter in color with body thin and slender. Other specimens also show con-
siderable variations in the punctation of face, interocellar area, and meso-
pleurum, color of legs and base of abdomen, and the length of ovipositor
sheath as compared to the fore wing length.
Distribution: Townes and Townes (1962) reported this species from
British Columbia, California (widely distributed), Oregon, Texas and Utah.
It is here reported from Idaho and Nevada for the first time.
Hosts: Chrysobothris mali, Myrmex arizonicus, Argilus angelicus.
2. CRYPTOHELCOSTIZUS NIGRICANS Townes and Townes
Cryptohelcostizus nigricans Townes and Townes, 1962. U.S. Natl. Mus.
Bull. 216(3): 508. o, °. Type: ¢, Arizona: Sierra Ancha, Parker
Creek (Townes). Examined, 1980.
Some of the salient features of this species are: Mesopleurum punctate,
S. Gupta: Genus Cryptohelcostizus (Ichneumonidae) 5
without striations or rugosities, but punctures close and deep. Propodeum
dorsally flat. Basal transverse carina of propodeum complete and evenly
arched. Nervulus basad of basal vein by 0.5 to 0.66 its length. Hind femur
polished and with very sparse hairs. Ovipositor about 0.7 as long as fore
wing. Ovipositor sheath about 0.45 as long as fore wing.
Black with reddish abdomen. Clypeus, base of mandible, and pronotum
each with a small white mark. Metascutellum and propodeum wholly black.
Wings hyaline. Legs black. First trochanter of fore leg without any white
mark. Apical two tarsal segments of hind leg brownish. First tergite black.
Specimens: 1%, 22. Arizona: Sierra Ancha, Parker Creek, ¢ (type),
May 7, 1947, H. & M. Townes (Townes). Workman Creek, “, ¢ (paratypes),
April 28, 1947, H. & M. Townes (Townes).
Distribution: U. 8. A.: Arizona.
3. CRYPTOHELCOSTIZUS MACULOSUS Townes & Townes
Cryptohelcostizus maculosus Townes and Townes, 1962. U. S. Natl.
Mus. Bull., 216(3): 512. ¢%. Type: ¢, California: Death Valley
(Washington). Reared from Prosopis. Examined, 1980.
The salient features of this species are: Mesopleurum closely and deeply
punctate with a few rugosities medially. Propodeum convex and sloping.
Basal transverse carina of propodeum interrupted medially, but its ends not
turned basad. Nervulus basad of basal vein by less than 0.5 its length.
Hind femur granulose with very sparse hairs. Ovipositor sheath about 0.5 as
long as fore wing.
Black, marked with yellow. Abdomen reddish-brown with whitish marks.
Face, clypeus, labrum, base of mandible, complete orbital stripe, temple,
pronotal collar, pronotum broadly above, a Y-shaped mark on middle lobe of
mesoscutum a crescentic mark on lateral lobe of mesoscutum, scutellum,
metascutellum, tegula, subtegular ridge, a broad oblong mark on mesopleurum,
metapleurum dorsally, a mark behind hind wing and propodeum apically,
yellow. Wings hyaline. Legs reddish-brown. Coxae black, dorsally marked
with white. First trochanter of fore leg ventrally white. First tergite basally
brownish and apically marked with white.
Specimen: California: Death Valley, ¢ (type), Sept. 3, 1957, R. C. Hall,
"Reared from Prosopis" (Washington).
Distribution: U. S. A.: California.
4. CRYPTOHELCOSTIZUS ORNATUS Cushman
Cryptohelcostizus ornatus Cushman, 1940. Proc. U. S. Natl. Mus.
88: 359. 2. Type: 2, Death Valley, California (Washington).
Examined, 1980.
The salient features of this species are: Mesopleurum closely and deeply
punctate. Propodeum convex. Basal transverse carina of propodeum inter-
rupted medially but ends not turning basad. Nervulus basad of basal vein by
less than 0.5 its length. Hind femur granulose with very sparse hairs. Ovi-
positor 0.6 the length of fore wing, its sheath 0.4 the length of fore wing.
Black with yellow marks. Abdomen reddish-brown. Face black. Clypeus
base of mandible, broad complete orbital stripes, an interrupted mark on
pronotal collar, upper part of pronotum, scutellum, metascutellum, tegula,
6 Contrib. Amer. Ent. Inst., vol. 19, no. 3, 1982
and subtegular ridge, yellow. Propodeum with two small white marks on
either side and a small mark basad of them. Wings hyaline. Legs reddish-
brown. Fore coxa dorsally and ventrally, and first trochanter ventrally white.
Middle coxa dorsolaterally and trochanter ventrally white. Hind coxa dorsally
white marked. Basal 0.7 of first tergite black.
Specimens: 2, %. Arizona: Sahuarito, “, April 11, 1947, H. & M.
Townes (Townes). California: Death Valley, ¢ (type) Feb. 23, 1939, M. F.
Gilman, reared from Chrysobothris deserta in desert holly (Washington).
Distribution: U. S. A.: Arizona, California.
Host: Chrysobothris deserta.
5. CRYPTOHELCOSTIZUS CAUDATUS Townes and Townes
Cryptohelcostizus caudatus Townes and Townes, 1962, U. S. Natl. Mus.
Bull., 216(3): 511. ¢. Type: California: Lake Tahoe (Davis).
Examined, 1980.
The characteristic features of this species are: Mesopleurum moderately
closely punctate, punctures arranged in transverse rows or forming fine
rugosities at places. Basal transverse carina of propodeum complete and
evenly arched. Hind femur with closely set hairs. Ovipositor as long as the
fore wing. Ovipositor sheath 0.75 as long as fore wing.
Black with reddish abdomen. Clypeus except its apical margin, base of
mandible, interrupted orbital ring, temple towards lower corner of eye,
upper margin of pronotum, two lateral marks on scutellum (meeting at apex),
metascutellum, tegula, subtegular ridge, and two sublateral marks on apical
slope of propodeum, whitish-yellow. Wings hyaline. Legs reddish-brown.
All coxae black with white dorsal marks. First trochanter of fore and middle
legs ventrally white marked. First tergite basally black.
Specimens: 22. California: Lake Tahoe, §¢ (type), Aug. 15, 1950,
R. M. Bohart (Davis). Oregon: Pinehurst, °, July 2, 1978, H. & M. Townes
(Townes). 7
Variation: The color of mesosternum in the specimen from Oregon is
somewhat lighter than that in the type. Otherwise it agrees with the same.
Distribution: U. S. A.: California, Oregon.
6. CRYPTOHELCOSTIZUS CHRYSOBOTHRIDIS Cushman
Cryptohelcostizus chrysobothridis Cushman, 1940. Proc. U. S. Natl.
Mus., 88: 358. %, &. Type: ¢, Stillwater, Oklahoma (Washington).
Paratype examined, 1980.
This species is characterized as: Mesopleurum with fine trans-rugosities.
Propodeum a little flat. Basal transverse carina of propodeum complete and
evenly arched. Hairs on front face of hind femur close together. Ovipositor
0.6 as long as fore wing. Ovipositor sheath 0.4 as long as fore wing.
Black. Abdomen reddish-brown. A mark on clypeus, a mark on pronotum
and an interrupted narrow orbital stripe, white. Metascutellum brownish.
Propodeum wholly black. Wings hyaline. Legs brownish, with all coxae
blackish. First trochanter of fore leg ventrally not marked with yellow.
Third and fourth tarsal segments of hind leg white. In male middle and hind
femora reddish-brown.
Specimen: Oklahoma: Stillwater, 2 (paratype), April 4, 1936, Myron
S. Gupta: Genus Cryptohelcostizus (Ichneumonidae) 7
Maxwell (Townes).
Host: Chrysobothris sp. in Malus pumila.
Distribution: U. S. A.: Oklahoma.
Il. THE DICHROUS GROUP
7. CRYPTOHELCOSTIZUS DICHROUS Viereck
Cryptohelcostizus dichrous Viereck, 1921. Psyche, 28:73. %, &.
Type:. 2, Southern Pines, N. C. (Cambridge).
This species is characterized by: Face granulose with punctures. Punc-
tures below antennal sockets obliquely striate. Hind margin of temple and its
occipital carina not bulged out at the lower margin of eye. Punctures on meso-
_pleurum deep and well separated. Prepectal carina reaching subtegular ridge.
Basal transverse carina of propodeum interrupted medially and turned basad.
Hind femur granulose with moderately dense hairs. Ovipositor 0.45 as long as
fore wing, shorter than in fumipennis and leiomerus. Ovipositor sheath about
0.35 as long as fore wing.
Black, abdomen reddish-brown. Orbital ring interrupted and white. Pro-
notum without any yellow mark. Wings black to strongly infumated. Legs
black. In male hind femur red.
Specimens: 42. North Carolina: Lumberton, ¢, Oct. 27, 1949, Rabb and
Townes. Council, 2, May 16, 1940, D. L. Wray. Page Lake, 2, Oct. 27,
1949, Rabb and Townes. Southern Pines, $, Oct. 1955, H. Townes (all in
Townes collection).
Distribution: Townes and Townes reported it from Georgia, Missouri,
New Jersey, North Carolina, Texas and Virginia.
8. CRYPTOHELCOSTIZUS GENALIS Townes and Townes
Female: Face shiny, punctate; punctures arranged in oblique striations
just below the antennal sockets. Vertex close to ocelli moderately closely
punctate. Hind margin of temple and its occipital carina strongly bulged
outwards at the level of lower corner of the eye. Mesopleural punctures
deep and separated by 0.4 their diameter. Prepectal carina reaching 0.6 the
height of mesopleurum. Propodeum basad of basal carina rugoso-punctate;
centrally punctato-striate to punctato-rugose. Basal transverse carina of pro-
podeum interrupted medially and its ends turned basad. Hairs on front face of
hind femur sparse. First abdominal tergite subapically grooved or not so;
groove punctate or impunctate. Ovipositor 0.5 as long as fore wing.
Black. Abdomen reddish-brown. Face black. A mark on clypeus, a small
mark on upper part of pronotum, a narrow interrupted orbital ring, anda
mark on pronotal collar, white. Wings infuscate. Coxa and trochanters
brownish-black. Legs reddish-brown. Hind tibia and tarsus brownish.
Two subspecies are recognized: C. genalis genalis Townes and Townes
from California and C. genalis niger, n. subsp. from Oregon.
8a. CRYPTOHELCOSTIZUS GENALIS GENALIS Townes and Townes
Cryptohelcostizus genalis Townes and Townes, 1962. U.S. Natl. Mus.
Bull., 216(3): 507. ¢. key, des. Type: ¢, California (Davis).
8 Contrib. Amer. Ent. Inst., vol. 19, no. 3, 1982
Female: Propodeum centrally rugoso-punctate. First abdominal tergite
subapically longitudinally grooved, groove shiny, impunctate.
Hind coxa brownish-black. Hind femur reddish-brown.
Specimen: California: Mendocino, Capella, ¢ (type), May 20, 1955, E. I.
Schlinger (Davis).
Distribution: U. S. A.: California.
8b. CRYPTOHELCOSTIZUS GENALIS NIGER, n. subsp.
Female: Face deeply and densely punctate, below antennal sockets punc-
tures sometimes appear semicircularly arranged. Malar space 0.79 the basal
width of mandible. Temple shiny with a few fine punctures, its hind margin
and occipital carina strongly bulged outwards at the lower corner of the eye.
Frons ruguso-striate. Vertex closely and deeply punctate with a few trans-
striae in the groove. Pronotal collar finely and closely punctate. Mesoscutum
deeply and closely punctate. Notaulus broad, with trans-striae. Scutellum
closely and deeply punctate, but punctures a little sparse in the middle. Meta-
scutellum shiny. Mesopleurum with moderately close and deep punctures.
Prepectal carina reaching 0.7 the height of mesopleurum. Metapleurum
punctato-striate. Basal transverse carina of propodeum interrupted medially
and its ends turned basad. Area basad of basal carina punctate submedially
and with a few trans-striations. Basolateral area of propodeum densely and
deeply punctate, central area punctato-striate, petiolar area rugose. Nervulus
basad of basal vein by less than 0.5 its length. Nervellus intercepted below
the middle. Hind coxa punctate. Hind femur with sparse hairs. First tergite
stout, closely and finely punctate. First sternite reaching up to spiracle.
Dorsolateral carina absent. Ventrolateral carina present and stout at base.
Second and following tergites weakly punctate to mat. Ovipositor 0.5 as long
as fore wing.
Black. Abdomen reddish-brown. Pronotal collar without white mark.
Small rounding mark on clypeus, and upper edge of pronotum, and a thin
broken orbital ring, white. Wings infuscate. Legs black, except the second
trochanter of each leg, which is reddish.
Male: Similar to the female in structure, but legs brownish-black and
first abdominal tergite a little darker in color. Wings not as dark as those of
females.
Length: ?, 16mm. Fore wing 11mm. Ovipositor6mm. ¢, 13 mm.
Fore wing 8mm.
Holotype: °, Oregon: Selma, May 28, 1978, H. & M. Townes (Townes).
Allotype: *, Oregon: Selma, May 20, 1978, H. & M. Townes (Townes).
Pavatypes: 12, 2%. Oregon: Pinehurst, °, June 29, 1978, H. &M.
Townes; 2%, same locality, dates, and collector as allotype (Townes).
Distribution: U. S. A.: Oregon.
9, CRYPTOHELCOSTIZUS LEIOMERUS Townes and Townes
Cryptohelcostizus leiomerus Townes and Townes, 1962. U. S. Natl. Mus.
Bull., 216(3): 506. &. key, des. Type: ¢, California (Berkeley).
The characteristic features of this species are: Face punctate, punctures
a little sparse and not forming striations. Hind margin of temple and its
occipital carina not bulged outward at the level of lower corner of eye. Vertex
sparsely punctate as compared to genalis, Punctures on mesopleurum close
S. Gupta: Genus Cryptohelcostizus (Ichneumonidae) 9
and forming trans-striations. Prepectal carina reaching 0.7 the height of
mesopleurum. Basal transverse carina of propodeum interrupted medially and
turned basad. Second abscissa of cubitus about 1.4 as long as the third abscis-
sa. Hairs on front face of hind femur sparse. First abdominal tergite
sparsely punctate. Ovipositor 0.6 as long as fore wing.
Black. Abdomen reddish-brown. Orbits narrowly white. Wings infuscate.
Legs brownish-black.
Specimen: California: Los Angeles, Pinhark Flats, ¢ (type), June 14,
1952, W. V. Garner (Berkeley).
Distribution: U. S."A.? California.
10. CRYPTOHELCOSTIZUS FUMIPENNIS Townes and Townes
Cryptohelcostizus fumipennis Townes and Townes, 1962. U. S. Natl. Mus.
Bull., 216(3): 507. 2. key, des. Type: ¢, Arizona (Washington).
This species can be recognized as follows: Face shiny, with distinct
punctures. Hind margin of temple and its occipital carina faintly bulged out-
ward. Vertex sparsely punctate as compared to genalis. Punctures on meso-
pleurum close and deep. Prepectal carina reaching 0.6 the height of meso-
pleurum. Propodeum rugoso-striate, its basal transverse carina interrupted
medially and the ends turned basad. Second abscissa of cubitus about 1.1 as
long as third abscissa. Hairs on front face of hind femur sparse. First ter-
gite closely punctate (sparsely punctate in leiomerus). Ovipositor 0.6 as long
as fore wing. |
Black. Abdomen reddish-brown. Clypeus except its apical margin, a
mark at the base of mandible, interrupted orbital ring, upper edge of pronotum,
pronotal collar medially, and tegula, white. Wings infuscate. Legs brownish-
black (including femur). Fore and middle legs a little lighter.
Specimen: Arizona: Sabino Canyon, "Resting on blossom", ¢ (type), Nov.
24, 1917, W. D. Edmonston (Washington).
Distribution: U. S. A.: Arizona.
ACKNOWLEDGMENTS
I am thankful to Dr. Henry Townes for providing me with facilities for
work and for his guidance during the course of the present research work.
Thanks are also due to the curators of various museums who loaned the types
for the present study.
10 Contrib. Amer. Ent. Inst., vol. 19, no. 3, 1982
REFERENCES
Ashmead, W. M. 1890. Description of New Ichneumonidae in the Collection of
the U. S. National Museum. Proc. U. S. Natl. Mus. 12: 387-451.
Carlson, R. W. 1979. Family Ichneumonidae. In Krombein ef al.: Catalog of
Hymenoptera in America North of Mexico. 1: 315-741.
Cushman, R. A. 1919. Description of New North American Ichneumon-flies.
Proc. U. S. Natl. Mus. 55: 517-543.
Cushman, R. A. 1922. New Species of Ichneumon-flies with Taxonomic Notes.
Proc. U. S. Natl. Mus. 60(21): 1-28.
Cushman, R. A. 1940. New Genera and Species of Ichneumon-flies with
Taxonomic Notes. Proc. U. S. Natl. Mus. 88: 355-372.
Gupta, V. K. 1970. Ichneumon Hunting in India pp. 1-80.
Townes, Henry K. 1944. A Catalogue and Reclassification of the Nearctic
Ichneumonidae (Hymenoptera). PartI. The Subfamilies Ichneumonidae,
Tryphoninae, Cryptinae, Phaeogeninae and Lissonotinae. Mem. Amer.
Ent. Soc., 11(1): 1-477.
Townes, Henry K. 1970. The Genera of Ichneumonidae, Part 2. (Gelinae).
Mem. Amer. Ent. Inst. 12: 1-537.
Townes, H. & M. 1951. In Muesebeck ef al.: Hymenoptera of America North
of Mexico - Synoptic Catalog. U. 8S. Dept. Agr. Agr. Monog.
No. 2: 1-1420.
Townes, Henry K. and Marjorie 1962. Ichneumon-flies of America North of
Mexico: 3. Subfamily Gelinae. Tribe Mesostenini. U. S. Natl. Mus.
Bull. 216(3): 1-602.
Vireck, H. L. 1921. Description of New Ichneumonidae in the Collection of
the Museum of Comparative Zoology Cambridge, Mass. Psyche
28(3): 70-83.
(SOUMOL @ SOUMOT, 139J8)
sisuapaweje SA ZILSOIIAJHOLdAYD
ee
9,
Wate
acper
er
cas
elias
at
tka
ih keg Tey
ras
r)
A
yea
A REVIEW OF THE GENUS PERITHOUS, WITH DESCRIPTIONS of NEW TAXA
(HYMENOPTERA: ICHNEUMONIDAE)
by
Virendra Gupta
Center for Parasitic Hymenoptera
Department of Entomology and Nematology
University of Florida, Gainesville, FL 32611
Perithous Holmgren is a small genus belonging to the tribe Theroniini, sub-
family Pimplinae (= Ephialtinae). It is mainly distributed in the Holarctic
Region. Hosts are aculeate Hymenoptera (larvae of Sphecidae, Vespidae, and
Chrysididae) in stems and twigs, particularly of Rosa and Rubus. There are
reports, however, of attacks on larvae of Xiphydriidae, Cerambycidae and
some Lepidoptera.
In this paper the world species are reviewed, with some new diagnostic
characters. The distributional ranges of the American and European subspe-
cies of P. mediator are analyzed. Three new species (digitalis, kamathi and
sundaicus) and two new subspecies (digitalis taiwanensis and divinator
himalayensis) are described from Kashmir and Himachal Pradesh in India
(areas of Palaearctic affinities) and Java and Taiwan (typically Oriental), thus
extending the known distribution of the genus to the Oriental Region.
_ Baltazar (1961) described Hybomischos as a subgenus of Pervithous from
the Philippines, distinguishing it mainly in having lateral spine-like teeth at
the base of first tergite, its spiracle distant from lateral carina, ovipositor
tip sinuate and thickened before apex, and by the absence of notauli in the
female. Aubert (1969) synonymized it with Perithous, while Constantineanu &
Pisica (1977) treated it as a distinct genus. Hybomischos is here considered
a separate genus. It is treated in an adjacent paper.
Genus PERITHOUS Holmgren (figs. 1-4)
Perithous Holmgren, 1959. Ofvers. Svenska Vetensk. -Akad. Forh.,
16: 123. Type-species: Ephialtes albicinctus Gravenhorst; designated
by Viereck, 1914.
Taxonomy: Oehlke, 1966: 279. Aubert, 1969: 100. Townes, 1969: 126.
Constantineanu & Pisica, 1977: 86.
Body moderately long and slender. General coloration black with mesoscu-
tum and mesopleurum often reddish and abdominal tergites narrowly margined
with yellow (Some species with black thorax). Legs pale brown. Face of male
whitish and of female black with whitish orbital borders.
Antenna moderately long and slender to shorter and a little thickened sub-
apically. Clypeus flattened apically and with a deep median apical notch. Man-
dibular teeth equal in length and similar in shape. Face a little convex,
sparsely to moderately punctate. Eyes only slightly emarginate just above
antennal sockets (cf. Hybomischos). Occipital carina complete, without a
median apical dip. Epomia short. Prepectal carina dorsad to 0.7 the height
2 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
of mesopleurum. Notauli weakly impressed anteriorly. Propodeum convex,
with only the apical transverse carina present, which is semicircularly
arched and usually complete. Fore wing with stub of ramellus distinct and
continued to some distance as a brownish or unpigmented groove. Areolet
triangular, receiving second recurrent vein near its outer corner. Nervellus
intercepted above the middle. Tarsal claws of female without a lobe or an
enlarged spatulate bristle. First abdominal tergite convex dorsally, with
short median dorsal carinae enclosing a basal declivity, its dorsolateral cari-
na present, and baso-lateral corner not projecting as a tooth. Spiracle just
below the dorsolateral carina and touching or almost touching it. First
sternite with a carina-like median fold, the basal end of which may or may
not be projecting out. Second to fifth abdominal tergites with low smooth
tubercles. Those on second often fused into a rhomboidal area. Ovipositor
0.8 to 1.5 x as long as the body, compressed, weakly upcurved, its tip with
lower valve occupying almost the entire depth, teeth compressed and close
together or spaced out to an area about 5.0 x the depth of ovipositor (figs.
1-3). Upper valve with slanting ridges, but not appearing saw-like in profile
view (cf. Hybomischos).
Some recent studies on Perithous are: Townes & Townes (1960), on North
American species; Townes, Momoi & Townes (1965), A Catalogue of Eastern
Palaearctic species; Oehlke (1966), on Taxonomy of Haupt species; Oehlke
(1967), Catalogue of Western Palaearctic species; and Constantineanu &
Constantineanu (1968) and Constantineanu & Pisica (1977), on Rumanian
species. Aubert (1969) also catalogued the West Palaearctic species, with
notes on hosts. These papers should be consulted for fuller bibliographic
references and synonymy of the species. Biological references mainly men-
tion host records and are given in the above references as well as in Carlson
(1979). Short (1978) figures the larval head of Perithous divinator divinator.
The larva has a large tooth-like projection at the junction of the base and
blade of the mandible and has three sensilla on maxillary and labial palpi
(fig. 4). In other genera of Theroniini, there are only 2 sensilla on these
palpi.
Species that have been described under Pevithous or those that belong to
that genus (in the strict sense) are listed below, with their present status.
Taxa that have been described as subspecies and are no longer considered
valid and other synonyms not originally described under Perithous are
omitted. These can be found in the various catalogues mentioned above.
Species falling under Hybomischos are also not included as they are being
treated in a separate paper that follows.
The following species have so far been reported under Perithous :
1. albicinctus (Gravenhorst), 1829. Europe, USSR, Japan.
Originally described under Ephialtes but transferred to Perithous by
Holmgren. Valid species.
2. brunnescens Koornneef, 1951. Europe.
Synonymized by Oehlke (1967) under Perithous (Hybomischos)
septemcinctorius (Thunberg).
3. divinator (Rossi), 1790. Europe, USSR, North Africa, North China,
North America.
Originally described under Jchneumon and first transferred to Perithous
by Marshall, 1872. Valid species. P. pimplavrius Haupt is a synonym
of it (cf. Oehlke, 1966).
13.
V. Gupta: Genus Perithous (Ichneumonidae) 3
exiguus Haupt, 1954. Europe.
Synonymized by Oehlke (1966) under P. (Hybomischos) septemcinctorius.
japonicus Uchida, 1928. Japan.
Reduced to a subspecies of P. mediator (Fabricius) by Townes & Townes
(1960). Valid subspecies.
longiseta Haupt, 1954. Europe.
Synonymized with P. mediator by Oehlke (1966). Constantineanu &
Constantineanu (1968) considered it a valid species, represented by
two subspecies longiseta longiseta Haupt and longiseta moldavica
Const. & Const. from Rumania. Not seen.
mediator (Fabricius), 1804. Holarctic.
Originally described under Pimpla and transferred to Perithous by
Holmgren, 1860. Townes & Townes (1960) recognized four subspecies
under it from Europe, North America, and Japan. Townes, Momoi &
Townes (1965) included nigrinotum Uchida from China as another sub-
species. Valid subspecies.
neomexicanus (Viereck), 1903. North America.
Originally described under Pimpla and first placed as a synonym of
P, pleuralis Cresson by Townes (1944) and subsequently (1960) treated
as a subspecies of P. mediator (Fabricius). Valid subspecies.
nigrinotum Uchida, 1942. China.
Townes, Momoi & Townes (1965) reduced it to a subspecies of
P. mediator. Valid subspecies.
nigrigaster Constantineanu & Constantineanu, 1968. Europe: Rumania.
pleuralis Cresson. North America.
Townes (1960) considered it as a subspecies of P. mediator.
Valid subspecies.
pimplarius Haupt, 1938. Europe.
Oehlke (1966) synonymized it with P. divinator (Rossius).
Constantineanu & Constantineanu (1968), however, considered it dis-
tinct. Not examined.
speculator Haupt, 1954. Europe.
Oehlke (1966), who examined the type considered it distinct.
Constantineanu & Constantineanu (1968) reported it from Rumania,
with two subspecies: speculator speculator and speculator trans-
sylvanicus. Not seen.
In addition the following species and subspecies are described here as new
from the Orient.
1,
2.
3.
4.
divinator himalayensis, n. subsp. Himachal Pradesh and Uttar Pradesh,
India.
digitalis, n. sp., with three subspecies:
(a) digitalis digitalis, n. subsp. Kashmir, India
(b) digitalis nepalensis, n. subsp. Nepal.
(c) digitalis taitwanensis, n. subsp. Taiwan.
sundaicus, n. sp. Java, Indonesia.
kamathi, n. sp. Himachal Pradesh, India.
4 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
PART I. THE HOLARCTIC SPECIES
Since all the European species so far described were not available for
study, a key to the world species is not attempted. Notes on all species known
to me are given below, incorporating new diagnostic features observed on the
metasternum, posterior mesosternal carina and the nature of the submeta-
pleural carina. These characters helped in the recognition of the new taxa
described in Part II of this paper.
1. PERITHOUS ALBICINCTUS (Gravenhorst)
Ephialtes albicinctus Gravenhorst, 1829. Ichneumonologia europaea,
3: 259. &. des. Type $, Germany: Hannover (Wroclaw).
Perithous albicinctus: Holmgren, 1860. Ofvers Svenska Vetensk.-Akad.
Forh., 16: 123. Uchida, 1928. J. Faculty Agr. Hokkaido Imp. Univ.,
20. 91.
Taxonomy: Townes et al., 1965: 69. Oehlke, 1967: 35.
Biology: Mirek, 1963: 419. Aubert, 1969: 100.
The posterior metasternal carina is curved and only slightly raised in the
middle, appearing like two low tubercles between the hind coxae. Median
metasternal furrow is deep and wide. Submetapleural carina is almost com-
plete to (but not quite touching) metasternal carina and flattened and wider just
above middle coxa (projection above middle coxa broadly rounded and its
anterior margin reflexed). Antennal flagellum composed of 37 segments,
slender. Ovipositor longer than body and its tip with teeth which are widely
spaced and occupying an area about 4.0 x its depth. First abdominal sternite
with only a moderately projecting basal tooth.
This species is distinctive in having a black thorax without reddish parts,
which is also the case in mediator japonicus from Japan, and sundaicus, n. sp.
described from Java.
Hosts: Ectemnius nigritarsus (H.-S.) (Hymenoptera: Sphecidae). Mirek
(1963) has published on the biology of this species.
Distribution: Europe (England, Germany, Poland, Belgium, Finland, |
Sweden, France, Austria, Czechoslovakia, Switzerland, Rumania, U. S. S. R.),
Japan. Specimens from Germany seen in Townes Collection.
2. PERITHOUS MEDIATOR (Fabricius)
The posterior metasternal carina is better developed and more prominent
in this species than in the preceding species. Tubercle-like prominences in
the middle are low but distinct. Median metasternal furrow narrow and some-
times partly obliterated. Submetapleural carina complete to metasternal
carina and forming a short conical projection above middle coxa (in American
subspecies this projection without a reflexed margin and somewhat broader
and thin; in Chinese subspecies also a little broader but reflexed). Ovipositor
longer than body and its tip with widely spaced teeth occupying an area about
..0 the apical depth of ovipositor. First sternite with a distinct conical or
obtuse projection at base, better developed than in albicinctus. Antennal flagel-
lum longer and slender (cf. divinator).
This species is widespread in Eurasia and North America. Five sub-
species are recognized (wediator, japonicus, nigrinotum, p leuvralis and
neomexicanus ). The non-reflexed nature of the submetapleural projection in
the North American subspecies readily separate them from the Eurasian
V. Gupta: Genus Perithous (Ichneumonidae) 5)
subspecies. The coloration of the various subspecies is diagnostic, although
the subspecies do show variations and perhaps intergrade in zones of overlap.
Some of the new subspecies described by Constantineanu & Constantineanu
have been synonymized with this subspecies by Aubert (1969) but this aspect
could not be verified as specimens of those subspecies were not available.
Key to the subspecies of Pevrithous mediator
Thorax wholly black except for yellow lines along upper margin of pronotum,
submetapleural ridge, mesepimeron, and apices of scutellum and meta-
scutellum. Hind tibia and tarsus blackish-brown and femur reddish-
brown, without any distinct black marks. Antenna black. Flagellar
segments 33+2. Japan, Korea, Sakhalin.
mediator japonicus Uchida (p. 7)
Thorax with mesopleurum and often also the mesoscutum reddish-brown.
Mesepimeron brown or black. Hind tibia and tarsus black marked.
Hind femur withor without black Marks... . 0.5 403 66 ew 85 8s 2
Mesopleurum with an oval yellow spot at dorsal end of prepectal carina.
Mesoscutum black. Scutellum largely yellow. Hind tibia and tarsus
pale yellow with blackish marks. Hind femur without black mark.
Face broadly yellow on sides. Antenna brown. Flagellar segments
28 (only 12 known). China: Manchuria.
mediator nigrinotum Uchida (p. 6)
Mesopleurum without a yellow spot. Mesoscutum usually wholly reddish-
brown, but sometimes brownish to blackish with reddish lines.
Specimens from North America with black mesoscutum also have apex
Of tind 16MWF DIAC. oie) oo wo is i SE ie we OG eae les 3
. Submetapleural projection above middle coxa conical and with a reflexed
margin. First abdominal tergite largely smooth with scattered minute
punctures. Second and following tergites also largely smooth in apical
half. All legs of female reddish-brown with only inconspicuous fuscous
marks on hind tibia and tarsus. Male fore and middle coxae may be
yellow. Antenna brown. Flagellar segments 31+3 (less in specimens
from Italy, which are comparatively smaller). Europe.
mediator mediator (Fabricius) (p. 6)
Submetapleural projection above middle coxa broader and withouta _ |
reflexed margin. First abdominal tergite with denser punctation; other
tergites also with crowded punctures, particularly in basal half. Hind
tibia and tarsus of female yellowish to brownish with conspicuous dark
fuscous marks. Fore and middle coxae partly whitish. Antenna black
in female, brownish black: in males: aicoand ees: 6 eee EG oe 4
Hind femur without a black apical mark (rarely faintly infuscate). First
abdominal tergite with punctures well-separated. Punctures on second
tergite crowded in its basolateral areas, but centrally (including
swellings) smooth and with widely scattered and minute punctures.
Mesoscutum usually reddish brown. Hind tibia and tarsus pale with
black marks. North America in Rocky mountains and west of them.
mediator neomexicanus (Viereck) (p. 8)
6 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
Hind femur always with an apical black ring. First and second abdominal
tergites with crowded punctures, those on second extending over the
basal half of swelling (except rarely particularly specimens from N. W.
partsof range). Mesoscutal color varying from reddish-brown to
black. Hind tibia and tarsus often dark. North America east of Rocky
mountains and Alaska and also in mountains of British Columbia and
Oregon (zones of overlap). ... mediator pleuralis (Cresson) (p.8)
2a. PERITHOUS MEDIATOR MEDIATOR (Fabricius)
Pimpla mediator Fabricius, 1804. Syst. Piez., 2: 117. ¥. des.
Type ?, Czechoslovakia: Mahren (Kiel, on deposit in Copenhagen).
Perithous mediator mediator: Townes & Townes, 1960. U.S. Natl.
Mus. Bull. , 216(2): 214. %, °. England, Germany.
Taxonomy: Oehlke, 1967: 35 (full synonymy).
Biology: Borries, 1897: 153-159. Brocher, 1926: 393-410. Aubert,
1969: 102.
Characterized by having punctures on abdominal tergites rather fine and
sparse. Submetapleural carina with a short conical projection above middle
coxa with its apical margin reflexed. Antenna brownish. Mesopleurum,
mesoscutum, scutellum (except apically), and often the upper dorsal margin
of pronotum reddish-brown (extreme apical margin of pronotum yellow); tegula
brown. Subtegular ridge yellow. Head black with inner orbital borders
yellow. All legs orange-brown with hind tibia and tarsus with rather incon-
spicuous light fuscous marks. Propodeum with a crescentic yellow mark in
the middle along apical transverse carina. Abdominal tergites narrowly
yellow along their apical margins.
Specimens from Italy are more yellow: face is largely yellow with black
mark confined in the middle (one female normal); clypeus is also largely
yellow; fore coxa is lighter in color and is yellowish; and the apical margins
of abdominal tergites are more distinctly yellow. Specimens from U. S. S. R.
almost lack the yellow mark on propodeum and the yellow apical bands on
abdominal tergites are rather narrow.
The males have the face wholly yellow, fore and middle coxae yellow,
their tibiae and tarsi also yellow but marked with orange, particularly femora,
and hind coxa and femur orange, their tibia and tarsus yellow with light fus-
cous markings. In one male from Italy there is a yellow faint spot on meso-
pleurum as seen in female of nigrinotum.
Hosts: Aubert (1969) gives a long list of hosts. They belong to Coleoptera
(Cerambycidae) and Hymenoptera (Xiphydriidae, Cynipidae, Chrysididae,
Eumenidae, Sphecidae, and Megachilidae).
Distribution: Widely distributed in Europe, England, USSR. Specimens
from USSR, Germany, Czechoslovakia, Italy, Denmark, Sweden, and England
seen in Townes and Ottawa Collections.
2b. PERITHOUS MEDIATOR NIGRINOTUM Uchida
Perithous medinator (!) nigrinotum Uchida, 1942. Ins. Matsumurana,
16: 118. 2. des. Type 2, China: Kaiyuan in Manchuria (Sapporo).
Examined, 1980.
Perithous (Perithous) mediator nigrinotum: Townes etal., 1965. Mem.
Amer. Ent. Inst., 5: 69.
V. Gupta: Genus Perithous (Ichneumonidae) 7
This subspecies is known only from the female type-specimen from
Kaiyuan (= Kaigen), Manchuria. It is rather similar to the typical subspecies
but the propodeum is shiny, impunctate, and the second and third abdominal
tergites are more definitely punctate, the punctures separated from each other
by about 1.5 to 2.0 their diameter. Facial punctures somewhat larger but
sparser than in mediator mediator. Submetapleural projection above middle
coxa not very acute, its margin narrowly reflexed. Face more yellowish on
sides, median black mark narrow towards antennal sockets (which are yellow).
Antenna brownish, yellowish ventrally towards base. Pronotum black with a
yellow line along its upper margin. Mesoscutum and metapleurum black.
Mesoscutum with faint brownish-yellow lines. Mesopleurum largely orange-
brown with a yellow spot near upper end of prepectal carina. Scutellum,
metascutellum, tegula, and subtegular ridge yellow. Propodeum black with a
broad crescentic yellow mark along apical transverse carina. Apices of all
abdominal tergites yellow. Fore and middle legs largely yellow with their
femorae yellowish orange. Hind leg orange-brown up to femur, its tibia and
tarsus yellowish and with fuscous marks subbasally and apically on tibia and
at apices of tarsal segments.
Distribution: China: Manchuria.
2c. PERITHOUS MEDIATOR JAPONICUS Uchida
Perithous japonicus Uchida, 1928. J. Fac. Agri. Hokkaido Imp. Univ.,
25:91. 9, oO. des., fig. Lectotype ?, Japan: Yamagata (Sapporo).
Japan: Sapporo, Nikko; Sakhalin.
Perithous mediator japonicus: Townes & Townes, 1960. U. S. Natl.
Mus. Bull., 216(2): 214. key, des. Japan.
Taxonomy: Townes et al., 1965: 69.
Similar to the typical subspecies in having an acute submetapleural projec-
tion above middle coxa with its margin reflexed. Propodeum punctate as in
mediator mediator. Facial punctures comparatively coarser and abdominal
tergites, particularly the first and second more densely punctate (first tergite
smoother with scattered punctures in mediator mediator and m. nigvinotum).
Facial orbits broadly yellow. Black mark on face parallel-sided
(variable in width). Thorax black except for yellow marks along upper margin
of pronotum, tegula (brownish-yellow), subtegular ridge, apical half of scutel-
lum, metascutellum, and a crescentic to circular mark on propodeum along
apical transverse carina. Apical margins of abdominal tergites yellow. Fore
and middle coxae yellow. Hind coxa reddish-brown. Fore and middle femora
yellowish-brown and their tibiae and tarsi infuscate. Hind femur reddish-
brown. Hind tibia and tarsus blackish-brown.
Distribution: Japan, Korea and Sakhalin. Specimens from Hokkaido,
Kamikochi and Tanigumi Prov., Japan,examined in Townes Collection.
Hosts: Unknown.
Alaskan specimens of mediator pleuralis somewhat approach this sub-
species in body punctation and color of hind leg. Japonicus also resembles
albicinctus in coloration, but submetapleural carina is complete and the basal
conical projection on first sternite is distinct. The submetapleural projection
above middle coxa is short, conical and with a reflexed margin.
8 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
2d. PERITHOUS MEDIATOR NEOMEXICANUS (Viereck)
Pimpla neomexicana Viereck, 1903. im Skinner: Trans. Amer. Ent.
Soc., 29: 88. 2. des. Type 2, Beulah, N. Mexico (Philadelphia).
Perithous mediator neomexicanus: Townes & Townes, 1960. U. S. Natl.
Mus. Bull., 216(2): 213.
Perithous (Perithous) mediator neomexicanus: Carlson, 1979. In
Krombein et al.: Catalog of Hymenoptera in America North of Mexico,
1: 348.
Biology: Parker and Bohart, 1966: 94.
This and the other American subspecies differ from the typical subspecies
in having a thin and broader submetapleural projection above middle coxa, the
apical margin of which is not reflexed. The punctation on abdominal tergites
is also denser. The fore and middle coxae are often partly yellowish-white
and hind tibia and tarsus with distinct black markings. The males are not
very distinctive, except that in males of neomexicanus, the antenna tend to be
dark brown to black and black markings on hind leg are more conspicuous.
First abdominal tergite with scattered punctures. Second tergite with
punctures confined mostly in basolateral areas. Swellings on it largely smooth
(cf. pleuralis and japonicus). Hind leg brown with tibia and tarsus broadly
infuscate (usually only the apices of tarsal segments black and tibia largely
yellowish-brown along inner side). Hind femur without black apical mark
(except rarely faintly so). Mesoscutum usually entirely reddish-brown.
Yellow markings on face, propodeum, and abdominal tergites as in the typical
sub-species.
Host: Pemphredon confertim.
Distribution: North America in Rocky mountains and west of the same.
Specimens from various localities in Alberta, Arizona, Idaho, Colorado,
California, Montana, Oregon, British Columbia, New Mexico and Washington
State seen in Townes and Ottawa Collections.
2e. PERITHOUS MEDIATOR PLEURALIS (Cresson)
Perithous pleuralis Cresson, 1868. Canad. Ent., 1: 46. 2. des.
Type ¢, Ontario: Grimsby (lost).
Perithous mediator pleuralis: Townes & Townes, 1960. U. S. Natl.
Mus. Bull., 216(2): 211.
Perithous (Perithous) mediator pleuralis: Carlson, 1979. In Krombein
et al.: Catalog of Hymenoptera in America North of Mexico, 1: 348.
Biology: Champlain, 1922: 97. Rheinhard, 1929: 155. Krombein, 1960:
31,
Readily distinguished from neomexicanus as well as from mediator
mediator by having crowded punctures on first and second abdominal tergites,
those on second tergite extending a little over the swellings, at least in basal
half (except rarely), hind leg brown with femur always having an apical black
ring which is usually wide, about as wide as the apical depth of femur, hind
tibia and tarsus yellowish with black apical marks, but often tibia and tarsus
with extensive black marks, color of mesoscutum varying from reddish-
brown to black, mesopleurum also often black dorsally, abdominal tergites
sometimes only with faint yellow margins, and fore and middle legs also
sometimes tending to be infuscate.
V. Gupta: Genus Perithous (Ichneumonidae) 9
Specimens from Alaska and British Columbia are generally darker, with
mesoscutum black, with or without two small reddish lines, hind femur with
wider black apical band, hind tibia and tarsus almost wholly black in female
and with white markings in male.
This subspecies intergrades with neomexicanus in the northern parts of
its distributional range and specimens of both the subspecies have been collected
in Oregon (same locality) as well as in British Columbia and Idaho.
Hosts: Pemphredon concolor, P. inornatus, and P. harbecki ?.
Distribution: North America east of Rocky mountains and Alaska. Also
occurring in British Columbia mountains, Idaho, and Oregon. Specimens from
most eastern states north to Michigan as well as Quebec seen in Townes
Collections.
3. PERITHOUS DIVINATOR (Rossi)
Ichneumon divinator Rossi, 1790. Fauna Etrusca,2: 48. 2. des.
Type ¢, Italy: Etrusca (location?).
Perithous divinator: Marshall, 1872. Catalog of British Hymenoptera,
p. 86. England.
Taxonomy: Townes & Townes, 1960: 215. Townes et al., 1965: 69.
Oehlke, 1967: 35. Carlson, 1979: 348.
Biology: Horstmann,1964: 193. Thomas, 1964: 199. Horstmann,1967: 95.
Aubert, 1969: 101.
In this species the median portion of posterior mesosternal carina forms a
posteriorly directed pair of closely set tubercles, which are also hairy,
metasternal furrow shallow to obliterated, submetapleural carina narrow,
complete to metasternal carina or slightly short of it, not widened above
middle, midventral fold of first sternite not forming a conical projection at
base, antenna short and a little thickened subapically, about 0.75 the length of
body, flagellum composed of 28+2 segments, ovipositor short, about 0.8 the
body length, its tip with teeth occupying an area which is only about 2.5 its
apical depth, teeth comparatively closely set, scape and pedicel combined a
little longer than second flagellar segment (14: 12), and nervellus intercepted
at its upper 0.33.
Head black with inner orbits, base of clypeus, mandible, and scape and
pedicel beneath, yellow. Upper margin of pronotum, subtegular ridge, apex
of scutellum, metascutellum and an arched mark on propodeum, yellow.
Mesoscutum, mesopleurum, mesosternum, and legs reddish-brown. Thorax
otherwise black. Hind tibia and tarsus often lightly infuscate. Abdominal
tergites black with apices of second and the following tergites narrowly to
faintly yellow. Sometimes these yellow lines partly obliterated.
In males, face wholly yellow and tegula and fore and middle legs largely
yellowish-white with hind tibia and tarsus blackish dorsally.
This species apparently has a wide range of distribution, having been
recorded from Europe, USSR, North Africa, North America and Northern
China. I have examined specimens of it from England, Sweden, Germany
and Eastern North America in Townes Collections and Canadian National
Collections. According to Townes & Townes (1960) it is an introduced species
in North America. ?
A new subspecies, divinator hymalayensis, is described here from
Himachal Pradesh, India. The European and American populations should
therefore be referred to as divinator divinator. a
Regional color variations occur in the various populations of divinator
divinatoy studied. The females from Sweden have two small yellow spots on
10 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
the face just below antennal sockets, connected to the yellow orbital stripes
(as is also seen in American specimens). In males the hind coxa is lightly
infuscate on the inner side. In all European specimens the tegula is yellowish-
brown, and hind tibia and tarsus faintly infuscate.
Specimens from England tend to be darker, with mesopleurum and meso-
scutum darker reddish-brown, fore coxa partly yellow, hind coxa largely infus-
cate, hind tibia and tarsus brownish-black, tegula dark brown in female and
brownish-yellow in male, and mesopleurum often black along prepectus and
along mesopleural groove (varying in extent in different specimens). The
yellow marks on abdomen and propodeum are extremely narrow and often
absent.
The North American specimens have bright reddish-brown mesopleurum,
mesoscutum, and all coxae of female (as in European specimens), except fore
coxae often partly yellow, the hind tibia and tarsus of female lightly infuscate,
tegula yellow, male fore coxa yellow, and yellow lines on abdomen and pro-
podeum more prominent. Even the orbital yellow stripes are a little wider
and often there are two small yellow spots below antennal sockets which may
be or may not be connected with the orbital stripes.
One female from Bulgaria: Sozopol, in Townes Collection, is rather
different and fits the description of Perithous pimplarius Haupt. The first
abdominal segment is short with a deep declivity at base and second and third
abdominal tergites are transverse (wider than long) rather than long as is
usual in the genus. The flagellum is short (27-segmented), scape and pedicel
combined not longer than second flagellar segment, abdominal tergites includ-
ing postpetiole more densely punctate, tubercles on abdominal tergites more
prominent and oblong, nervellus intercepted almost at middle, tegula yellowish-
white, scutellum largely yellow and apex of first tergite white (never seen in
the specimens of divinator with me), and yellow lines on abdominal tergites
more distinct.
Whether or not this specimen represents one of the species described by
Haupt or Constantineanu could not be decided without reference to the type-
specimens. Horstmann (1967) has incidentally shown that the nature of the
abdomen in divinator can vary with reference to its hosts, and therefore he
synonymized P, pimplarius with divinator.
Hosts: Chiefly parasitic on species of Pemphredon, Passoloceus, Psenulus,
Trypoxylon, and other Sphecidae in Europe and North America. Aubert (1969)
lists several hosts belonging to Coleoptera (Cerambycidae), Lepidoptera
(Pyralidae), and Hymenoptera (Cynipidae, Chrysididae, Eumenidae, and
Sphecidae).
Distribution: Europe (Italy, Germany, France, England, Finland, Rumania,
Czechoslovakia, Spain, USSR), North Africa, China, Canada, U.S.A. In
North America distributed mainly from Quebec south to Connecticut and
Pennsylvania and west to Wisconsin.
V. Gupta: Genus Perithous (Ichneumonidae) 11
II. DESCRIPTIONS OF NEW TAXA FROM THE ORIENT
Key to the Oriental Species of Perithous
1. Mesopleurum and mesoscutum black with yellow spots or stripes, finely
polished. Metapleurum and metasternum also polished. Submeta-
pleural carina flattened out and forming a triangular or rounded pro-
jection over baee.of middle come tig, (it. 6 ee ee ew we 2
Mesopleurum and mesoscutum reddish-brown, subpolished. Metapleurum
with minute punctures or smoother (digitalis). Metasternum smooth or
hairy. Submetapleural carina narrow and not flattened or widened
above middle coxa (fig. 2, 3) more reflexed. .........2e.e6-. 3
2. Metasternal carina forming conical projections in the middle between hind
coxae (fig. 1). Median metasternal groove absent and represented by
a small pit only. Submetapleural carina distinct on anterior 0.8 of
metapleurum and forming a triangular projection above middle coxa.
First sternite conically produced basomedially. Mesoscutum with two
lateral yellow stripes near middle. Propodeum smooth dorsally, with
only scattered punctures laterally. (In general thorax sparsely hairy
and highly polished). Java (2 only known).
5. sundaicus, n. sp. (p. 15)
Metasternal carina not forming conical projections in the middle. Median
metasternal groove distinct and widely open behind between hind coxae
(metasternal carina curving around hind coxae). Submetapleural carina
short, extending only in anterior 0.5 of metapleurum and forming a
broadly rounded flange above middle coxa. First sternite not conically
produced basomedially, only with a short tubercle. Mesoscutum wholly
black. Propodeum more punctate dorsolaterally. (In general thorax
hairy and subpolished.) India: Himachal Pradesh. (% only known.)
6. kamathi, n. sp. (p.16)
3. Metasternum shiny and with a finger-like projection between middle and
hind coxae (fig. 3). Submetapleural carina broadly reflexed above
middle coxa and forming a short triangular projection. Antenna 0.8 as
long as the body, slender. Ovipositor 0.8 to 1.0 as long as body, its
tip with very closely spaced oblique teeth (fig. 3). Base of first sternite
with a forwardly directed projection. (Female only known.) India,
Nepal. Tal wates wince tine Ves winaebin 4. digitalis, n. sp. (p. 13)
Metasternum apically rough and hairy, with a posteriorly directed pair of
closely set and blunt tubercles between hind coxae (fig. 2). Submeta-
pleural carina narrowly reflexed and broadly triangular above middle
coxa. Antenna shorter, about 0.65 to 0.75 the body length and some-
what thickened preapically. Ovipositor about 0.8 as long as the body,
its tip with moderately spaced vertical teeth (fig. 2). Base of first
sternite without any projection. ........ | A RCOR: 5) a in te
4. Tegula brown or with a brown spot (in American populations yellow). Side
of scutellum and middle coxa reddish-brown. Abdominal yellow bands
very narrow, often incomplete or absent on some or most of thetergites.
Body slender, 7-9 mm.long. Submetapleural carina complete to hind
coxal cavity, straight. Metapleurum not strongly striate near hind coxa.
12 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
Male without yellow marks on mesoscutum or mesopleurum. Widely
distributed in Holarctic Region. 3a. divinator divinator Rossi (p. 9)
Tegula, sides of scutellum, and middle coxa largely yellow. Abdominal
yellow bands always prominent. Body stouter, 10-11 mm long. Sub-
metapleural carina a little obliterated posteriorly and bent inwards.
Metapleurum obliquely striate near hind coxa (fig. 2). Male with
yellow marks in the region of notauli and on mesopleurum. Hind tibia
and tarsus tending to be darker. India: Himalaya.
3b. divinator himalayensis, n. subsp. (p. 12)
3b. PERITHOUS DIVINATOR HIMALAYENSIS, n. subsp. (fig. 2)
Female: Antenna a little thickened preapically, about 0.65 to 0.75 as long
as the body. Face punctate in the center, smooth along orbital borders, its
upper edge a little cleft between antennal sockets. Frons, vertex, temple and
occiput smooth and shiny, but hairy, especially the temples. Mesoscutum sub-
polished, beset with short hairs. Pronotum shallowly wrinkled in the median
groove, otherwise subpolished. Mesopleurum polished, sparsely hairy. Meta-
pleurum polished, with minute punctures dorsoapically, area close to hind
coxa ruguloso-striate (fig. 2). Submetapleural carina narrow and not widened
above middle coxa, a little obliterated apically, where it is bent inward and
meets metasternal carina which forms two closely set posteriorly directed
teeth-like projections (fig. 2). This area also conspicuously hairy. Median
groove on metasternum distinct in apical 0.75. Propodeum finely punctate
dorsolaterally, smooth basomedially. Apical transverse carina complete or
slightly obliterated in the middle, bounding a smooth and shiny petiolar area.
Propodeum with a shallow median groove up to the transverse carina. Abdo-
minal tergites subpolished with scattered punctures, those on first distributed
all over except in the apical portion, those on second weaker in apical half,
those on third and the following tergites confined to basal 0.25 with tubercles
and apical areas mat to subpolished. Sides of tergites densely punctate.
Tubercles rather weak and more distinct only on tergites 3-5. Ovipositor
about 0.8 the body length, its tip with parallel, slightly arched teeth confined
to an area about 2.5 its depth (fig. 2).
Black with mesopleurum, mesosternum, mesoscutum and scutellum
reddish-brown. Scape and pedicel yellow ventrally. Flagellum brown. Basal
two to three flagellar segments also yellowish ventrally. Face laterally and
just below antennal sockets, upper orbital borders, clypeus along basal and
lateral margins, mandible in basal half, upper margin of pronotal collar,
tegula, subtegular ridge, sides and apex of scutellum, metascutellum, mese-
pimeron, and a semicircular mark on propodeum along apical transverse
carina, yellow. Legs reddish-brown except fore and middle coxae yellow,
their femora yellow marked and hind tibia and tarsus blackish-brown. Second
to fifth abdominal tergites yellow apically. Margins of sixth and seventh ter-
gites broadly yellow laterally and very narrowly so dorsally.
Male: Similar to female with face and clypeus wholly yellow. Mesoscutum
with yellow marks along notaular areas. Scutellum largely yellow. Meso-
pleurum with indistinct one or two yellow marks. First tergite may be yellow
apically in the middle.
This subspecies differs from the typical subspecies in having the submeta-
pleural carina almost obliterated apically and metapleurum more punctate.
The tubercles are mat. The male has faint to distinct yellow marks on
mesoscutum and mesopleurum. The body coloration is more like that of the
V. Gupta: Genus Perithous (Ichneumonidae) 13
American population of the typical subspecies. The European populations tend
to have less yellow on propodeum and abdomen. The abdomen is comparatively
strongly punctate. Specimens from Britain examined are rather dark and
largely devoid of yellow markings.
Length: 10-11 mm. Fore wing 7.5-8.5 mm. Ovipositor 7.5-8.0 mm.
Antenna 7.0-7.5 mm.
Holotype °, India: Himachal Pradesh: Manali, 1828 m., 19-V-1970,
M. K. Kamath (Gupta).
Allotype ¢: Same data as the holotype.
Paratypes: 262, 4%: Same locality as the type, but collected from 2 to 30-
V-1970 by various Collectors (Gupta). H. P.:Sangla, 2743 m., Kalpa Valley,
12, 16 - VI-1972, Gupta. U.P.: Gangotri, 3000 m., 12, 20-VI-1977,
G. Singh (Gupta).
4, PERITHOUS DIGITALIS, n. sp. (fig. 3)
Readily distinguished by having a finger-like median projection on meta-
sternum between middle and hind coxae, submetapleural carina narrow, but
rather broadly reflexed and triangular above middle coxa, this carina a little
curved near metasternal carina, first abdominal sternite with a median basal
projection, and ovipositor tip compressed and with teeth spaced close together
(fig. 3).
Female: Antenna slender, about 0.8 the body length. Face minutely to
closely punctate, raised near antennal sockets and with a faint median carina
extending in the upper half of face. Clypeus smooth, with setiferous punctures
and concave in apical half. Frons and vertex smooth and polished. Vertex
posteriorly and temple smooth but hairy. Pronotum polished. Mesoscutum
subpolished and hairy. Scutellum a little more convex than in other species
and subpolished. Mesopleurum polished, sparsely hairy. Metapleurum
polished. Submetapleural carina narrow and forming a short triangular pro-
jection anteriorly above middle coxa, just short of reaching posterior meta-
sternal carina. Metasternal carina irregular and forming a characteristic
posteriorly directed long finger-like projection (fig. 3) in the middle, with its
apex knob-like. Metasternum without a median longitudinal groove. Propodeum
shiny, hairy or punctate on sides, with or without a median basal depression;
its apical transverse carina complete or incomplete. First tergite smooth or
punctate, raised in the middle. First sternite with a strong basomedian for-
wardly directed projection. Abdomen with protuberances on second and the
following tergites, which may be smooth or punctate. Ovipositor rather
strongly compressed, about 0.8 to 1.0 the body length, teeth on its lower
valve compressed into a small area, occupying about 2.5 its maximum depth,
teeth circular and close together, with basal 2-3 teeth divergent (fig. 3).
This species is known only from three females, one each from India, Nepal
and Taiwan. They are essentially similar to each other, but exhibit slight
differences in puncation and coloration. I prefer to consider them as allopatric
subspecies until the extent of variability of each population is known, when they
may turn out to be distinct species. Among the three specimens, the specimen
from Kashmir has stronger punctation, while the specimens from Nepal and
Taiwan are closely related. They can be separated by the following key:
14 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
Key to the subspecies of Perithous digitalis
1. Inner eye orbits narrowly yellow. Face closely punctate. Propodeum
without a white apical semicircular mark. Apical transverse carina
distinct and semicircularly arched. Median groove on propodeum
extending to its middle. Propodeum punctate laterally. Hind coxa
yellowish-brown with a pale yellow dorsal spot. Scape and pedicel
black. Bands on abdominal tergites narrow, those on apical tergites
rather inconspicuous. India: Kashmir.
4a. digitalis digitalis, n. subsp. (p. 14)
Inner orbits broadly yellow—these stripes meeting on face below antennal
sockets. Face with minute scattered punctures. Propodeum with a
complete semicircular yellow stripe in the region of apical transverse
carina, or with two lateral spots, the carina itself indistinct and
represented by two lateral tubercles. Median groove of propodeum
indistinct to absent. Propodeum smoother. Scape and pedicel white
marked. Bands on abdominal tergites wider and conspicuous on second
ane tre FOLlOWInS Lererice. oe ei ee ee eer er 2
2. Face with scattered punctures, smooth medially. Propodeum smooth and
shiny, with two apicolateral yellow spots. Hind coxa and femur yellow.
Hind leg largely yellow with fuscous marks on tibia and tarsus.
Wena se Ea ee A 4b. digitalis nepalensis, n. subsp. (p. 15)
Face with minute punctures, without a smooth medial area. Propodeum
with a semicircular yellow mark in the region of apical transverse
carina, with minute setiferous punctures laterally. Hind coxa and
femur yellowish-brown. Hind leg darker yellowish-brown, with tibia
extensively black marked. Taiwan. .
4c. digitalis taiwanensis, n. subsp. (p. 15)
4a. PERITHOUS DIGITALIS DIGITALIS, n. subsp.
Female: Face with distinct well separated punctures. Metapleurum
wrinkled near hind coxa, otherwise smooth and polished. Propodeum shallowly
punctate laterally, with a median groove which extends to its middle; its apical
transverse carina distinct and semicircularly arched. Petiolar area mat.
First tergite punctate with its apex smoother. Protuberances on second and the
following tergites smooth medially, otherwise abdomen sparsely punctate and
hairy. Sides of tergites with denser punctures.
Black. Mesoscutum, scutellum (except its apex), and mesopleurum
(except narrowly below wings), reddish-brown. Clypeus along epistomal
groove, mandible basally, inner orbits narrowly up to the ocellar level, hind
corner of pronotum, tegula, subtegular ridge, apex of scutellum, metascutellum
wholly, and apices of second to sixth abdominal tergites narrowly, yellow.
Mesepimeron brownish-black. First tergite faintly yellow in the middle and
seventh tergite yellow laterally. Scape and pedicel without yellow marks,
black. Fore and middle legs largely yellowish with yellowish-brown patches
on femora. Hind coxa yellowish-brown with a pale yellow dorsal oval spot.
Hind femur yellowish-brown with a black subapical ring and its apex yellow.
Middle and hind tibiae with black dorsal lines, and their bases and apices also
black. Middle and hind tarsal segments yellow with their apices black.
Male: Unknown.
V. Gupta: Genus Perithous (Ichneumonidae) 15
Length: ?, 8.5mm. Fore wing 7mm. Ovipositor 8.5 mm.
Holotype: 2, India: Kashmir, Pahalgam, 7200 ft., 29-VI-1966,
M. K. Kamath (Gupta).
4b. PERITHOUS DIGITALIS NEPALENSIS, n. subsp.
Female: Face with scattered punctures, smooth medially. Metapleurum
smooth and polished. Propodeum smooth and shiny, with a faint indication of
a basomedian groove, its apical transverse carina absent, but represented
laterally by weak tubercles. Petiolar area smooth and shiny. First tergite
largely smooth and shiny. Protuberances on second and the following tergites
impunctate and shiny. Second to fourth tergites punctate laterally.
Black. Similar to digitalis digitalis but inner eye margins broadly yellow
—these marks meeting on face below antennal sockets. Scape and pedicel with
ventral whitish-yellow marks. Upper margin of pronotum yellow. Upper mar-
gin of mesopleurum broadly black. Mesepimeron yellow. Apex of propodeum
with two small lateral yellow marks. Hind leg largely yellow with lateral
black marks on femur, tibia and tarsus. Hind coxa faintly marked laterally
with yellowish-brown. Bands on second and the following abdominal tergites
wider and conspicuous on all tergites.
Male: Unknown.
Length: °, 8mm. Fore wing 7mm. Ovipositor 6.6 mm.
Holotype 2, Nepal: Kathmandu, Godavari, 1500 m., 29-IX-1970, Gupta
(Gupta).
4c. PERITHOUS DIGITALIS TAIWANENSIS, n. subsp. (fig. 3)
Female: Face with minute punctures, without a smooth smooth median
area. Metapleurum smooth and polished. Propodeum with minute setiferous
punctures laterally, with a faint indication of a basomedian groove, without an
apical transverse carina, though with lateral weak tubercles. Petiolar area
mat. Abdomen smooth as in nepalensis, with smooth tubercles and second to
fourth tergites punctate laterally.
General coloration similar to that of digitalis nepalensis, with scape,
pedicel and abdominal tergites broadly yellow. Yellow on face more extensive
below antennal sockets. Propodeum with a semicircular yellow mark in the
region of apical transverse carina. Hind leg somewhat darker, yellowish-
brown, with femur almost wholly yellowish-brown and tibia more extensively
black marked.
Male: Unknown.
Length: 2, 8.5mm. Fore wing 7.5mm. Ovipositor 7.5 mm.
Holotype: °, Taiwan: Taipei, ex Chiu Colln., 1971 (Gupta).
5. PERITHOUS SUNDAICUS, n. sp. (fig. 1)
Superficially resembling the Japanese Perithous mediator japonicus in
coloration, but distinct in having a yellow spot on mesopleurum near upper end
of prepectal carina and also by having a very polished metapleurum and meta-
sternum, with the posterior metasternal carina forming distinct conical
processes in the middle and the median metasternal groove absent and repre-
sented only by a small pit. The submetapleural carina is absent in apical
0.25 and the projection above middle coxa is conical and longer than in japoni-
cus, The propodeum is shiny and not punctate as in japonicus.
16 Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
Female: Antenna slender, about 0.8 as long as the body. Face with
scattered shallow punctures. Frons, vertex, temple and occiput smooth
and shiny. Temple with scattered hairs. Mesoscutum shiny, with minute seti-
ferous punctures. Pronotum, mesopleurum, metapleurum, mesosternum
and metasternum shiny and polished. Mesopleurum with scattered minute
setiferous punctures. Metasternal carina forming conical projections in the
middle between hind coxae. Median metasternal groove indistinct and repre-
sented by a pit only. Submetapleural carina distinct in anterior 0.8 of meta-
pleurum, forming a triangular projection above middle coxa, its apical margin
reflexed. Propodeum smooth and shiny, with scattered and a little elongate
punctures laterally, with a shallow median groove. Apical transverse carina
erased medially, although two triangular white marks at this place demarcate
a semicircular petiolar area. Tergite shiny, with scattered punctures lateral-
ly. First sternite forming a conical projection basomedially. Punctures on
second to fourth tergites moderate and well separated. The following tergites
smooth with minute setiferous punctures. Teeth on ovipositor tip arched and
parallel, extending over to nearly 5.0 the width of ovipositor (fig. 1).
Black. Antenna wholly blackish-brown, without white marks on scape
and pedicel. Face except narrowly in the middle, clypeus except in the middle,
teeth except apically, upper orbital borders, two linear marks on mesoscutum,
upper margin of pronotum, pronotal collar largely, subtegular ridge, an oval
spot on mesopleurum at upper end of prepectal carina, mesepimeron, two
lateral triangular marks on propodeum in the region of apical transverse
carina, scutellum laterally and apically, and metascutellum except basally,
yellow. Tegula brown. Fore and middle coxae and fore trochanters yellow.
Hind coxa reddish-brown with an oval dorsal yellow spot at base. Legs other-
wise brownish-yellow, with fore legs lighter in color and middle tarsus and
hind tibia and tarsus brownish-black. Apices of first (narrowly), 2nd and 3rd
tergites brownish, those of fourth laterally, fifth completely and sixth and
seventh tergites laterally, yellow.
Male: Unknown.
Length: °, 12mm. Fore wing 10mm. Ovipositor 15 mm.
Holotype 2, Java: Tjibodas, 1400 m., 27 to 29 - VII - 1930, M. A.
Lieftinck (Townes).
Paratype 2, W. Java: Mt. Gedeh, 28 - XI - 1935, ex Betrem Coll.
(Gupta).
6. PERITHOUS KAMATHI, n. sp.
Similar to the Javanese sundaicus, n. sp., and mainly distinguished by the
absence of conical tubercles on metasternum and first sternite, complete
metasternal groove, which is widely open behind between hind coxae, and
short submetapleural carina extending in anterior 0.95 to 0.6 only and forming
a broadly triangular flange above middle coxa. The propodeum is punctate
dorsolaterally and the apical transverse carina is distinct throughout. The
mesoscutum does not have yellow stripes.
Male: Antenna long and slender, about 0.8 as long as the body. Face
punctate. Frons, vertex, temple and occiput smooth, with temple and vertex
posteriorly sparsely hairy. Mesoscutum subpolished, with short hairs.
Pronotum, mesopleurum, metapleurum, and metasternum shiny, polished,
with mesosternum subpolished and more hairy (as in mesoscutum). Metaster-
nal carina almost absent, faintly represented in the middle, not forming coni-
cal projections. Median metasternal groove distinct and widely open behind.
V. Gupta: Genus Perithous (Ichneumonidae) 17
Submetapleural carina extending in anterior 0.5 to 0.6 only and forming a
broadly triangular flange above middle coxa. Propodeum with distinct well
separated punctures except in the central region, its median groove faint.
Apical transverse carina distinct. First tergite with scattered punctures, its
sternite with a blunt projection at base. Second to fifth tergites more punctate,
punctures well separated. The following tergites progressively minutely
punctate.
Black. Scape and pedicel yellow beneath. Flagellum black. Face and
clypeus wholly, upper orbital borders, pronotal collar medially, upper margin
of pronotum, subtegular ridge, an oval spot on mesopleurum at the end of
prepectal carina, mesepimeron, apical half of scutellum, metascutellum, two
triangular marks on propodeum near apical transverse carina, and apices of all
abdominal tergites, yellow. Tegula yellowish-brown. Fore and middle coxae
and trochanters yellow, their femora, tibia and tarsi yellowish-brown. Hind
coxa and femur orange brown, coxa yellow basodorsally, tibia and tarsus black-
ish. Apical tarsal segment of middle tarsus also black.
Female: Unknown.
Length: >, 11-14mm. Fore wing 8-11 mm.
Holotype: %, India: Manali, Himachal Pradesh, 1828 m., 20-V-1970,
M. K. Kamath (Gupta). |
Paratypes: 7%, same locality, collected during 17 to 23-V-1970 (Gupta).
REFERENCES
1. Aubert, Jacques -F. 1969. Les Ichneumonides Ouest-Palearctiques et
leurs hotes. 1. Pimplinae, Xoridinae, Acanitinae. Ouvrage Publee
avec le Concours du CNRS Pp 1-304.
2. Baltazar, C. R. 1961. The Philippine Pimplini, Poemeniini, Rhyssini,
and Xoridini (Hymenoptera: Ichneumonidae, Pimplinae). Monogr.
Natl. Inst. Sci. & Technol. Manila 7: 1-130.
3. Borries, H. 1897. Om Pevrithous mediator og Omalus auratus. Vidensk.
Medde. Dansk. Naturh. Foren. 1897: 153-159.
4. Brocher, Fr., 1926. Observations sur la Perithous mediator Gr. Ponte,
Oeuf, larve, Nymphe et Imago. Etude anatomique de la tariere, de
ses muscles et de son fonctionnement. Ann. Ent. Soc. France 95: 393-
410.
5. Carlson, R. W. 1979. Family Ichneumonidae. Jn Krombein, ef. al.:
Catalog of Hymenoptera in America north of Mexico 1: 315-740.
6. Champlain, A. B. 1922. Records of Hymenopterous Parasites in
Pennsylvania. Psyche 29: 95-100.
7. Constantineanu, M. I. & Constantineanu, R. M. 1968. Contributions
a Ll'etude du genre Perithous (Hym., Ichneum.) de la R. S. Romania.
Zool. Anz. 180(3-4): 228-258.
8. Constantineanu, M. I. & Pisica, Constantin, 1977. Fauna Republicii
Socialiste Romania. Insecta, Hymenoptera, Ichneumonidae 9(7): 1-310.
18
af.
12.
13.
14.
19.
16.
ae
18.
19.
20.
Zi,
22.
23.
Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
Danks, H. V. 1971. Biology of Some Stem-Nesting Aculete Hymenoptera.
Trans. R. Ent. Soc. London 122: 323-399.
Haupt, H. 1938. Die Pimplinen der Schlupfwespen- Fauna von Bellinchen
(Oder). Mark. Tierwelt 3(3): 181-221.
Haupt, H. 1954. Fensterfange bemerkenswerter Ichneumonen. Deutsch.
Ent. Ztschr (n.f.) 1: 99-116.
Horstmann, K. 1964. Zur Biologie der Holzanbohrenden Schlupfwespen,
Perithous divinator Rossi (Hym., Ichneum.). Fauna Mitt. Norddeutschl.
2: 193-197.
Horstmann, K. 1967. Untersuchungen uber eine Wirtsbedingte
Modification bei der Schlupfwespen Pevithous divinator (Rossi) (Hym.,
Ichneum.). Zool. Anz. 178: 95-102.
Krombein, K. V. 1960. Biological Notes on some Hymenoptera that
Nest in Sumach Pith. Ent. News 71(2-3): 29-36; 63-69.
Mirek, J. 1963. Zweiter Fund von Pevithous albicinctus (Gravenhorst)
in Polen Samt Angaben Uber andere Arten der Gattung Perithous
Holmgren (Hymenoptera, Ichneumonidae). Fragm. Faunist. 10: 419-
423
Oehlke, J. 1966. Revision der Ephialtinae-Typen von H. Haupt (Hymenop-
tera, Ichneumonidae). Reichenbachia 6(32): 279-285.
Oehlke, J. 1967. Westpalaartische Ichneumonidae. I. Ephialtinae.
In Junk: Hymenopterorum Catalogus (nova editio), part 2: 1-48.
Parker, F. D. & Bohart, R. M. 1966. Host-Parasite Associations in
some Twig-Nesting Hymenoptera from Western North America.
Pan-Pacific Ent. 42: 91-98.
Rheinhard, E. G. 1929. Pemphredon and her enemies. Nature Mag.
13: 155-157.
Short, J. R. T. 1978. The final larval instars of the Ichneumonidae.
Mem. Amer. Ent. Inst. 25: 1-508. (Perithous on pages 25 and 173).
Thomas, S. J. 1964. Pevrithous divinator Rossi and its host, Pemphredon
lethifer Shuckard. Michigan Acad. Sci., Arts & Letters 49: 199-201.
Townes, H. 1944. A Catalog and Reclassification of the Nearctic Ichneu-
monidae (Hymenoptera), Part I. The subfamilies Ichneumoninae,
Tryphoninae, Cryptinae, Phaeogeninae and Lissonotinae. Mem. Amer.
Ent. Soc. 11(1): 1-477.
Townes, H. & M. 1960. Ichneumon-flies of America North of Mexico:
2: Subfamilies Ephialtinae, Xoridinae, Acaenitinae. U. S. Natl.
Mus. Bull. 216(2): 1-676.
V. Gupta: Genus Perithous (Ichneumonidae) 19
24. Townes, H., Momoi, S. & Townes, M. 1965. A Catalog and Reclassifica-
tion of Eastern Palearctic Ichneumonidae. Mem. Amer. Ent. Inst.
5: 1-661.
29. Townes, H. 1969. The Genera of Ichneumonidae, Part I. Ephialtinae to
Agriotypinae. Mem. Amer. Ent. Inst., 11: 1-300.
Figs, 1-8
20
Contrib. Amer. Ent. Inst., vol. 19, no. 4, 1982
4. Larval head of Perithous divinator divinator
(After Short, 1978)
A STUDY OF THE GENUS HYBOMISCHOS
(HYMENOPTERA: ICHNEUMONIDAE)
by
Virendra Gupta
Center for Parasitic Hymenoptera
Department of Entomology and Nematology
University of Florida, Gainesville, FL 326ll
Hybomischos was originally described by Baltazar (1961), as a subgenus of
Perithous. However, the differences in the nature of the ovipositor tip,
notauli, first tergite, etc., justify its generic separation. Baltazar described
from the Philippines two species: Perithous (Hybomischos) galbus and
virgulatus. Townes et al. (1965) placed in it a Eurasian species, septemcinc-
torius Thunberg. Constantineanu and Constantineanu (1968) described five
additional taxa from Rumania (septemcinctorius rufatus, yvomanicus romanicus,
romanicus rufigaster, transversus transversus and transversus trapezoidalis).
Perithous exiguus Haupt, P. brunnescens Koornneef, and P. septemcinctorius
mevidionatoy Aubert were synonymized with semptemcinctorius by Oehlke
(1966, 1967). In the Townes Collection, there are specimens of septemcinc-
torvius from Europe and North America, type of galbus from the Philippines,
and specimens of an undescribed species from Japan, which is described
below as Hybomischos townesorum, n. sp. The type of virgulatus Baltazar
has been examined in the U. S. National Museum, Washington. The species
from Rumania are unknown to me.
Genus HYBOMISCHOS Baltazar
Perithous (Hybomischos) Baltazar, 1961. Monogr. Natl. Inst. Sci. &
Tech. Manila, 7: 49. Type-species: Perithous (Hybomischos) galbus
Baltazar; original designation.
Taxonomy: Townes et al., 1965: 69. Constantineanu & Constantineanu,
1968: 250. Aubert, 1969: 101 (as a syn. of Perithous). Constantineanu
& Pisica, 1977: 92 (as a separate genus).
Rather similar to Perithous, but lower mandibular tooth acute. Upper tooth
with a wider cutting edge. Eyes emarginate just above antennal sockets.
Notauli absent. Apical propodeal carina absent to faintly visible. Propodeum
strongly convex, granulose to sparsely or distinctly punctate, usually with a
weak or fairly distinct median groove. Submetapleural carina forming a flange
along anterior half of metapleurum, absent posteriorly (type-species), or bent
inwards toward posterior metasternal carina, which is, however, weak and
not fully formed. Sometimes submetapleural carina appears forked posteriorly
due to a carina-like rugosity connecting it to the hind coxal cavity. Nervellus
intercepted at or above the middle. First abdominal tergite flat or convex
dorsally, granulose or punctate, its median dorsal carinae absent, but at
base forming lateral tooth-like projections. Spiracle of first tergite below and
2 Contrib. Amer. Ent. Inst., vol. 19, no. 5, 1982
and distant from the dorsolateral carina. Ovipositor about 1.4 to 2.0 the body
length, its tip strongly compressed and sinuate; teeth on lower valve weaker,
subvertical to semicircular; upper valve with saw-like teeth on upper edge.
Hybomischos has the same type of ovipositor as does Atvactogaster i.e.,
the tip being sinuate. The latter genus, however, is distinct in having the
lower mandibular tooth longer than the upper, clypeus with a median subapical
point, spiracle of first tergite situated just above the dorsolateral carina and
touching the same, eyes only very slightly emarginate (as in Perithous), and
propodeum with a semicircular carina separating a smooth petiolar area (as
in Perithous). Pevrithous is further distinguished from Hybomischos by the
presence of notauli, absence of lateral tooth-like projections at base of first
tergite, spiracle of first tergite touching or almost close to the dorsolateral
carina, and ovipositor tip different and not sinuate.
Biological references on Hybomischos are few and deal mainly with host
records of the European H. septemcinctorius, which are larvae of aculeate
Hymenoptera, similar to those parasitized by species of Pevithous. Nothing
is known about the larval morphology.
Species of Hybomischos appear to form two species groups: In septem-
cinctorius and townesorum, the nervellus is intercepted at the middle (or just
above it), antennal flagellum is shorter and thicker, about 0.5 the body length,
male flagellum is with tyloids, teeth on ovipositor tip angled at 60°, and sub-
metapleural carina appears forked posteriorly. In galbus and virgulatus (both
from Philippines), the nervellus is intercepted above the middle, flagellum is
as long as the body and slender, submetapleural carina is not forked posteri-
orly, and teeth on ovipositor tip angled at 30° from the horizontal. The males
are unknown. The Rumanian species are unknown to me.
1. HYBOMISCHOS GALBUS (Baltazar) (figs. 1-3)
Perithous (Hybomischos) galbus Baltazar, 1961. Monogr. Natl. Inst.
Sci. & Tech. Manila, 7: 50. ¢. Key, des., fig. Type ¢, Philippines:
Luzon, Nueva Ecija, Sierra Madre Mts. (TOWNES). Examined, 1980.
Paratype $, Luzon, Laguna, Mt. Bahanao.
This and the other Philippine species (virgulatus) are readily distinguished
from H. septemcinctorius and townesorum, n. sp., by the characters men-
tioned under species groups. Baltazar (1961) has provided a key to distinguish
the two.
H, galbus is characterized by having a yellowish body color with abdomen
a little brownish, without any black marks. First tergite convex dorsally
(fig. 1) and granulose. Flagellum long and slender, about as long as the body.
Teeth on lower valve of ovipositor semicircularly arched and the basal tooth
very much slanting, making an angle of 30° with the horizontal axis. Nervellus
intercepted above the middle. Propodeum granuloso-punctate, with a distinct
basomedian groove. Abdominal tergites 2-5 coarsely punctate.
Distribution: Philippines: Luzon. Known so far by the type-specimens
only.
2. HYBOMISCHOS VIRGULATUS (Baltazar)
Perithous (Hybomischos) virgulatus Baltazar, 1961. Monogr. Natl. Inst.
Sci. & Tech. Manila, 7: 50. °. key, des., fig. Type ?, Basilan
(Washington). Examined, 1980.
V. Gupta: Genus Hybomischos (Ichneumonidae) 3
Readily distinguished from galbus by having three black stripes on meso-
scutum. Frons in middle, ocellar region, tubercles on abdominal tergites, and
middle of first tergite also black. First abdominal tergite flatter dorsally
and shiny. Propodeum with only a few scattered punctures. Abdominal ter-
gites punctate only laterally. Ovipositor 1.8 x the body length. Otherwise
related to H. galbus.
Distribution: Philippines: Basilan. Known by the type specimen only.
3. HYBOMISCHOS SEPTEMCINCTORIUS (Thunberg)
Ichneumon septemcinctorius Thunberg, 1922 (1824). Mem. Acad. Imp.
Sci. St. Petersburg, 8: 280; 9: 363. 2. des. Lectotype 9, Sweden(Uppsala)
Taxonomy: Oehlke, 1967: 36. Torgersen, 1972: 99. Townes et al. , 1965: 70.
This species, originally described under Ichneumon from Sweden and first
placed under Pervithous by Roman (1912) is fairly well distributed in Europe
and USSR. Constantineanu & Pisica mention Japan also in its distributional
range, but I could not find a reference to that effect. Togerson (1972)
reported it from North America for the first time by a single specimen found
by him in Ann Arbor, Michigan, in a spider web inhis garage. Subsequently,
only three more females from North America have been caught: One in
Ann Arbor by H. Townes in his garage, one in Ottawa, Canada, at light by
him, and another in Canada by Mike Sanborne at Stillsville, Ont., ina Malaise
trap.
This species is characterized by having flagellum short and a little thick
in the middle. Male flagellum with tyloids on segments 9-15. Face sparsely
to minutely punctate. Thorax reddish with yellow markings. Propodeum
granulose, with a weak median groove. Nervellus intercepted at the middle or
at upper 0.4. First abdominal tergite granulose, flat dorsally. Abdominal
tergites moderately punctate, punctures well separated from each other.
Teeth on lower valve of ovipositor weak and angled at 65° from the horizontal.
Distribution: Europe, Russia, North America.
Hosts: (From Aubert, 1969): Andricus quercus -tozae (Cynipidae);
Omalus auratus (Chrysididae); Pemphredon lugubris, P. morio, Psen
(Mimumesa) dahlbomi, and Psenulus fuscipennis (Sphecidae). These hosts
have been reported in Europe.
4. HYBOMISCHOS TOWNESORUM, n. sp.
Female: Face with scattered punctures, smoother laterally along orbital
borders. Frons, vertex, temple, and occiput smooth and shiny, with
scattered hairs, particularly on temple. Mesoscutum subpolished and with
small hairs. Pronotum, mesopleurum, mesosternum, and metapleurum
polished. Mesosternum more hairy than other parts. Submetapleural carina
short and flange-like in anterior half and forked posteriorly, one arm of which
is continuous with striations along hind coxal cavity. Propodeum strongly con-
vex, apical half almost vertical, punctate; punctures evenly separated and
mostly in the middle; its apical transverse carina incomplete and poorly
defined; petiolar area smooth. Nervellus intercepted near middle. First
abdominal tergite with scattered punctures, which are a little more crowded
subapically. Second tergite with sparse scattered punctures. The following
tergites progressively less punctate and smoother. Sides of second to fourth
tergites with crowded punctures. Ovipositor about 1.35 x as long as the body,
4 Contrib. Amer. Ent. Inst., vol. 19, no. 5, 1982
its tip sinuate and strongly compressed. Lower valve with faint or very faint
teeth, which are slanting at an angle of 60° with the horizontal. Upper valve
with 6-7 saw-like teeth on upper edge.
Black. Scape and pedicel yellow ventrally, flagellum brownish-black. Face
along orbits, upper orbital borders up to slightly beyond the ocellar area,
clypeus wholly, mandible except apically, basolateral corners of mesoscutum,
hind corner of pronotum, tegula, subtegular ridge, scutellum except basally,
metascutellum, a crescentic mark on propodeum in the region of apical trans-
verse carina, and apices of all abdominal tergites, yellow. Apical mark on
first tergite short. Fore and middle coxae and trochanters yellow. Rest of
fore and middle legs yellowish-brown, with their femora with brownish patches.
Middle femur darker and apices of its tarsal segments blackish. Hind coxa
brownish with black mark basodorsally and yellow apically; femur orange-red;
tibia and tarsus blackish-brown with basal and apical tarsal segments yellowish-
white in basal 0.5 to 0.75.
Male: Essentially similar to the female except that face is wholly yellowish-
white. Flagellum pale brownish, segments 9-17 with linear tyloids. Second to
fourth abdominal tergites more densely punctate. Hind leg lighter in color:
coxa yellow apically, femur light orange, tibia whitish medially.
Length: 2, 9mm. Fore wing 6-7 mm. Ovipositor 11.5-12 mm. ¢, 7.5
mm. Fore wing 5.5 mm.
Holotype: 2, Japan: Mt. Norikura, 1600 m, 31-VII-1954,Townes family
(Townes).
Allotype “, Japan: Sapporo, 9-VIl-1954, Townes family (Townes).
Paratype 2, Japan: Kamikochi, 22-VII-1954, Townes Family (Townes).
Hybomischos townesorum is related to H. septemcinctorius in the nature of
nervellus, antennal flagellum and submetapleural carina, but can be readily
distinguished by its black thorax, punctate propodeum without a distinct median
groove, sparsely punctate frist tergite, and the following tergites with scattered
shallow punctures and smoother on apical half.
LITERATURE CITED
Aubert, Jacques - F. 1969. Les Ichneumonides Ouest-Palearctiques et leurs
hotes. I. Pimplinae, Xoridinae, Acaenitinae. Ouvrage Publee avec la
Concours du CNRS Pp 1-304.
Baltazar, C. R. 1961. The Philippine Pimplini, Poemeniini, Rhyssini and
Xoridini (Hymenoptera, Ichneumonidae). Monogr. Natl. Inst. Sci.
Tech. Manila 7: 1-130.
Constantineanu, M. I. and R. M. 1968. Contributions a letude du genre
Perithous (Hym., Ichneum.) dela R. S. Romania. Zool. Anz. 180
(3-4): 228-258.
Constantineanu, M. I. and Pisica, Constantin, 1977. Fauna Republicii
Socialiste Romania. Insecta, Hymenoptera, Ichneumonidae, 9(7): 1-310.
Oehlke, J. 1966. Revision der Ephialtinae-Typen von H. Haupt (Hymenoptera,
Ichneumonidae). Reichenbachia 6(32): 279-285.
V. Gupta: Genus Hybomischos (Ichneumonidae) 5
Oehlke, J. 1967. Westpalaartische Ichneumonidae I. Ephialtinae. In Junk:
Hymenopterorum Catalogus (nova editio), part 2: 1-48.
Townes, H., Momoi, S., and Townes, M. 1965. A Catalog and Reclassifica-
tion of Eastern Palaearctic Ichneumonidae. Mem. Amer. Ent. Inst.
5: 1-661.
Torgersen, T. R. 1972. A Pevrithous (Hymenoptera Ichneumonidae) introduced
from Europe. Great Lakes Ent. 5(3): 99.
Hybomischos galbus (Baltazar)
Fig.)
REVISION OF THE NEW WORLD GENUS HADROMEROPSIS PIERCE
(Coleoptera, Curculionidae, Tanymecini)
by
Anne T. Howden
Department of Biology, Carleton University,
Ottawa, Ontario, K1S 5B6, Canada
ABSTRACT
The genus Hadromeropsis Pierce is revised; included are a review
of the nomenclature, taxonomy, a key to the species, illustrations,
distribution maps, and a discussion of the morphology of the male and
female genitalia.
The genus is divided into two subgenera: the nominate subgenus
Hadromeropsis, type-species nobilitatus (Gyllenhal), and the new
subgenus Hadrorestes, type-species pectinatus n. sp. Of the 52
Species assigned to the genus 35 are described as new. The-species in
the nominate subgenus are as follows: opalinus (Horn) from Arizona and
Mexico; fulgens (Champion) from Mexico; crinitus n. sp. from Mexico;
flagellatus n. sp. from Mexico; dejeanii (Boheman) from Mexico;
amoenus n. sp. from Mexico; scintillans (Champion) from Guatemala and
Mexico; micans (Champion) from Guatemala; brevicomus n. sp. from
Mexico; aureus (Blanchard) from Bolivia; cretatus (Champion) from
Costa Rica and Panama; rufipes (Champion) from Costa Rica; superbus
(Heller) from Argentina; gemmifer (Boheman) from Colombia, Costa Rica,
Guatemala, Panama, and Venezuela; meridianus n. sp. from Brazil and
Colombia; batesi n. sp. from Bolivia, Brazil, and Peru; togatus
(Boheman) from Brazil and Paraguay; argentinensis (Hustache) from
Argentina, Brazil, Paraguay, and Uruguay; plebeius n. sp. from Brazil;
pulverulentus n. sp. from Brazil; pallidus n. sp. from Argentina,
Brazil, araguay, and Uruguay; speculifer n. sp. from Brazil;
beverlyae n. sp. from Brazil; nobilitatus (Gyllenhal) from Argentina
and Brazil; atomarius (Boheman) from Brazil; excubitor n. sp. from
Brazil; and fasciatus (Lucas) from Brazil. The species in the
subgenus Hadrorestes are as follows: alacer n. sp. from Colombia and
Ecuador; inconscriptus n. sp. from Peru; nebulicolus n. sp. from
Colombia; silaceus n. sp. from Colombia; exilis n. sp. from Bolivia;
impressicollis (Kirsch) from Colombia; institulus n. sp. from Ecuador;
ombycinus n. sp. from Peru; brachypterus n. sp. (locality unknown);
transandinus n. sp. from Ecuador; nanus n. sp. from Ecuador; apicalis
n. sp. from Ecuador; dialeucus n. sp. from Venezuela; contractus n.
sp. from Bolivia; pectinatus n. sp. from Bolivia, Colombia, and Peru;
conquisitus n. sp. from Ecuador; scambus n. sp. from Ecuador; magicus
(Pascoe) from Brazil (?) and Colombia; nitidus n. sp. from Ecuador;
mandibularis n. sp. from Colombia; spiculatus n. sp. from Bolivia and
Peru; picchuensis n. sp. from Peru; and cavifrons n. sp. from Peru.
The new species earinus from Ecuador and striatus from Colombia are
not assigned to a subgenus. Species synonymized are: Hadromerus
scabricollis Faust, a synonym of gemmifer (Boheman); Hadromerus
brachispinosus Boheman, a synonym of togatus (Boheman); Hadromerus
herbaceus Lucas, a synonym of fasciatus ucas); Hadromerus ruficrus
Melee he Hadromeropsis subaeneus Voss, synonyms of impressicollis
Kirsch).
11 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Lectotypes are designated for opalinus (Horn), fulgens sea
scintillans (Champion), micans (Champion), superbus (Heller),
brachispinosus (Boheman), argentinensis (Hustache), fasciatus (Lucas),
and herbaceus (Lucas).
TABLE OF CONTENTS
Introduction
HIS COG1Gar: REV EW. ijcns wares wares 6s 21h 4G bas bale 0 oS Se os wo ewe Gieid se aisle apa « le
Material. SHUGIGG. cic io vacances « sents <eies 0 eh bi uF 0 els SA lees © OTS 2
Methods, Amd TEM TO VOGV ces » ce cree wtnscrereusls 0 6, coca eteteiowisiee s wa gie he 5
Morphology of Male-and Female Genitalia. oo. cscs ccicneceiev ec ccewiine s /
1 O OIG caey © sincere ee so be Ate ois © + sie eine o Caiels © beans sc ete eee ee dae 10
T axonomy
Genus HadromMeropsisS PICVCE...cecececsceccccrscccvsccesveveseseces 11
REY TO SCE ACS 4 wid oot) sa wie Ph Fo Mite cols Geis annie ele carers so BEN AS Teo '4is ERNE 12
Subgenus HadromeropsisS PICLCE....cecesevevccccccevreccresccvcccves 24
The opalinus Group.......e.6. 24
1, .Qpa linus; LHOFN) sess: cee 25 15... MEG dans: Nl. .SD.~ . s.caee 54
2. fulgens (Champion)...... 27 1G, bates N. SPivwe so seaees 55
o. CRAPACUS Min SD. whiewaus s 29 |
4. flagellatus n. Sp. wee. 30 The argentinensis Group....5/,58
The scintillans Group........ 34 17. togatus (Boheman)........ 58
18. argentinensis (Hustache).60
5. dejeanii (Boheman)...... 34 19. plebeius fl. SD. os eine were 62
6. -GMOGHUS. Mi. oSDics io eines ce ese a 20. pulverulentus n. sp. ....65
7. scintillans iencaeh) 21 DG LIONS AE. SPs; sesen soa sO
8. micans (Champion)....... i Je VSRCCUII ter 1. SP i dxcarees 69
O.. DREVILCOMUS, Nes SDe. «oe ess 42 23. beverlyae N. Sp. ..ccceee 72
10. aureus (Blanchard)...... 44
11. cretatus (Champion)..... 46 The nobilitatus Group......... ha
12. rufipes (Champion)...... 48
13. superbus (Heller)....... 49 24. nobilitatus (Gyllenhal)..74
25. atomarius Bonena sieshaivene's 76
The gemmi fer Group. ..s.< sexes ok 26. excubitor n.. Sp. sssesces 78
27. fasciatus caw Rae pe eas 80
14. gemmifer (Boheman)...... 51
Howden: Hadromeropsis iii
Subgenus Hadrorestes n.subg...83
The alacer Groupius.ss eee nae o4 The pectinatus Group. .ies. sss 104
205 @1acer Me SPs sees Cree 85 AO. Ca OUCIS Ne SPs ieee wees 105
<9. INCONSCriplus A. Sp. ...8/ Hi, CONLVACTUS Ti SD. Sis deine 106
30. nebuUlICOlUS 1°80. 4.545 88 42. PeCctinatus NN. SP. cxeewas 108
Sl. STT@CCUS Ti Soy wivere cs 90 43. CONGUISITUS N. SP. .0.s0- 110
44. SCANDUS Ne SDe! bi ex a ee ues aie
Ene @X311S Growl .. 5. veeacess 92 45. magicus (Pascoe)......... 114
FOL ATES Te Se yee ie en 115
B25 CRU TS Me Spe a ee erewees oe 47. mandibularis n. sp. ..... 117
48. spiculatus W. Sp. isso 119
The impressicollis Group..... 93
Species Unassigned to Group...121
33. impressicollis (Kirsch).94
34. INSEIRUIUS We SD oe ears vs 96 49. PICCHUENSTS NM. SPs seve 2%
39. DOMDYCINUS fic SP. a.ceas 97 OU. CAVITPONS Ne S06 awd ce eas 122
36. brachypterus n. sp. ....98
Species Incertae Sedis......... 124
The transandinus Group....... 99
o1. COP INUS Ms SD« wan soe ees 124
37. transandinus n. sp. ...100 Oe, SEC IOUS ‘Te BDA we ie wees 126
304 NAnNUS Ws! BO. a eeawinlse wa 102
OO BPICANTS BS SB es! esa 103
Pe GRIOW VG CGI ounce cisee scarps 4 sin wade Gd We Gk OA Sk PR EASA A eS 128
meer ataie CU EOMy.. 5 4a:s.0dgy sede ale eae we WINS i ERA RO RMA a Me Oe 128
Peres 6 UGB Osi sibel cL aah ewes y Puck + ee Ca oe RON Re ues 132
Baar Ee Be aia a scatter apa sania aka Minlava aoy Wace Wiuts Keak ae ee a ae woes 176
Cm
Rey
Sty ayy
Fig. 1. H. (Hadromeropsis) nobilitatus (Gyllenhal),
type-species of Hadromeropsis. Male, dorsal habitus.
Howden: Hadromeropsis ;
REVISION OF THE NEW WORLD GENUS HADROMEROPSIS PIERCE
(Coleoptera, Curculionidae, Tanymecini)
by
Anne T. Howden
HISTORICAL REVIEW
There has been considerable nomenclatural confusion involving the
use of Hadromerus Schoenherr, Hadromeropsis Pierce, and Siderodactylus
Schoenherr, partly due to various interpretations of the Titerature
and partly because the original very obscure description of Hadromerus
has apparently been overlooked by many authors, including me.
In 1823, column 1141, Schoenherr first published "96. Hadromerus
nob. Typ.: Curc. sagittarius Oliv." This bare reference, without
description, is nonetheless a valid indication according to Art.
l6a(v) of the International Code (1964). Thus sagittarius Olivier,
1807, from Senegal, is fixed as the type-species of Hadromerus
Schoenherr, 1823, by original designation and _ monotypy. The
Characters of the genus are first described and discussed by
Schoenherr in 1826 (pp. 136, 137) where he lists nobilitatus from
Brazil for the first time as "Typus" of Stirps la and sagittarius
Olivier from Senegal as "Typus" of Stirps 2a. However, there is no
description of nobilitatus here, other than the description of Stirps
la; this is interpreted as Stirps la being a subgenus’ but invalid
here since nobilitatus is a nomen nudum. Thus, in this second
publication, nothing was changed nomenclatural ly.
In 1833 (p. 12), Schoenherr in his "Tabula synoptica," lists
Hadromerus much as he did in 1823: "Genus 102. Hadromerus. Nob. Typus:
Hadr. sagittarius. Curc. id. Oliv."
In 1834, Schoenherr (p. 125) first published the name
Siderodactylus citing, "Hadromerus Schh. olim (1).-Curculio Oliv.,"
"(1) Schh. Curc. Disp. Meth. p.137. Hadromerus, stirps 2.,": and
listing sagittarius as the type. Thus, Siderodactylus is a synonym of
Hadromerus Sch., 1823. Added to the genus Siderodactylus at this time
were adstringatus Gyll. n. sp. and rhodinus Gyll. n. sp., both from
Senegal. On p. 127, Schoenherr (1834) describes Hadromerus citing,
Poenh, Circ. Disp. Meth., « bs: 130,...n0,,.69,. Cstc]”™ as the original
description. On p. 128 (loc.cit.) nobilitatus is first described by
Gyllenhal, and no other species added.
Pierce, 1913, p. 400, tried to resolve the confusion by stating,
"For the genus with nobilitatus as type we may take a new name,
Hadromeropsis." It is fortunate that Pierce discussed the problem and
stated the type-species clearly, because he accidentally cited
Schoenherr, 1834, p. 125, the page for the sagittarius-based genus
instead of the nobilitatus-based genus (p.127), to receive the new
name.
* I thank Richard T. Thompson, London, for bringing this to my
attention.
2 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Marshall (1952:261-262) disagreed with Pierce, but Marshall's
reasoning would be disallowed by the International Code published
subsequently in 1964.
Since Pierce's publication of the name Hadromeropsis in 1913, the
name has been applied to the New World genus in most of the literature
including Giinther and Zumpt (1933), Blackwelder (1957), Hustache
(1938), and Van Emden (1944). Exceptions to this usage are Heller
(1921), Hustache (1928), Marshall (1952), and Kuschel (1955). Based
on taxonomic characters, all Hadromerus are African and all
Hadromeropsis are New World.
In both Gtinther and Zumpt (loc. cit.: 102-103) and Blackwelder
(loc. cit.: 800), six nomina nuda are listed: as synonyms of
Hadromeropsis. I have not repeated these names with the valid species
but record them here. They are as follows: “Hadromerus irroratus
Klug" and "Hadromerus pygalpis Germar' listed by Boheman as nomina
nuda of his atomarius (Boheman, 1840:292); "“Hadromerus micronychus
Germar" listed by Bonheman as nomen nudum of his brachispinosus [=
togatus Boheman] (Boheman, 1840:291); "Hadromerus lepidopterus Klug"
listed by Boheman as a nomen nudum of his dejeanii (Boheman,
1840:293); "Hadromerus splendidus Salle” listed by Champion as a nomen
nudum of his fulgens (Champion, 1911:184); and "Hadromerus schonherri
Chevrolat" listed by Champion as a nomen nudum of his scintillans
(Champion, 1911:182).
Taxa originally associated with Hadromeropsis but which have been
subsequently removed include the following:
Hadromerus porosus Boheman, 1840:294, transferred to Pandeleteius by
Kuschel (1955:280).
Hadromerus tuberculifer Boheman, 1840:295, transferred to Pandeleteius
by Kuschel (1955:280) then to Airosimus by Howden (1966:202).
Pandeleteinus Champion as a subgenus of Hadromeropsis, sensu Voss
(1954:232), reinstated as genus by Howden (1969:76).
Taxa originally associated with Hadromeropsis HERE REMOVED from
the genus are the following:
Hadromeropsis distinctus Voss, 1954:232 here removed to Pandeleteius.
PanEE toi distinctus (Voss), NEW COMBINATION.
Hadromeropsis griseus Voss, 1954:233 here removed to Pandeleteius.
Pandeleteius griseus (Voss), NEW COMBINATION.
MATERIAL STUDIED
This study was based on over 2000 specimens in 35 institutional
and private collections. Institutional collections are referred to in
the text by the city in which they are located, and private
collections by the owner's name.
Institutional collections studied and the persons assisting are as
follows:
Auckland New Zealand Arthropod Collection, DSIR.
G. Kuschel.
Basel Naturhistorisches Museum. W. Wittmer.
Berkeley
Berlin
Buenos Aires
Cambridge
Chicago
Curitiba
Dresden
Eberswalde
Hamburg
Ithaca
Leiden
London
Los Angeles
Maracay
Mexico
New York
Ottawa
Oxford
Paris
Howden: Hadromeropsis
California Insect Survey. E. Sleeper.
Museum flr Naturkunde an der Humboldt-
Universitdt. F. Hieke.
Museo Argentino de Ciencias Naturales.
M. J. Viana.
Museum of Comparative Zoology, Harvard
University. uJ. Lawrence and M. Thayer.
Field Museum of Natural History. H.
Dybas and R. Wenzel.
Universidade Federal do Paran&. G. H.
Rosado Neto.
Staatliches Museum fur Tierkunde.
R. Hertel and R. Krause.
Deutsche Akademie der Landwirtschaft-
swissenschaften zu Berlin. G. Morge.
Universitat Hamburg. H. Striimpel.
Cornell University. L.L. Pechuman.
Rijksmuseum van Natuurlijke Historie
J. Krikken.
British Museum (Natural History).
R. Thompson.
Natural History Museum of Los Angeles
County. R. Snelling.
Universidad Central de Venezuela.
F. Fernéndez-Yepez and L. Joly.
Instituto de Ecologia. G. Halffter.
American Museum of Natural History.
P. Vaurie.
Canadian National Collection. D. Bright.
Hope Department of Entomology.
University Museum. E. Taylor and
M. W. R. Graham.
Muséum National d'Histoire Naturelle.
H. Perrin.
4 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Pittsburgh Carnegie Museum. G. Wallace.
Rosario de Lerma Instituto de Investigaciones
Entomologicas Salta, INESALT, Argentina
(formerly INESAN, San Miguel). A.
Martfnez, M. J. Viana, G. J. Williner.
Sacramento California Department of Food and
Agriculture. A. Hardy and T. Seeno.
San Francisco California Academy of Sciences. H.
Leech and D. Kavanaugh.
San José University of Costa Rica. A. Wille.
S%0 Paulo Universidade de S40 Paulo. S. A. Vanin.
Stockholm Naturhistoriska Riksmuseet. L.
Janzon and P. I. Persson.
Tucson University of Arizona. F. Werner.
Tucuman Instituto Miguel Lillo. A. Willink.
Washington United States National Museum of
Natural History. D. R. Whitehead.
The following individuals generously loaned material from their
private collections:
Henry Hespenheide, Los Angeles, California.
Charles O'Brien, Tallahassee, Florida.
Warren Steiner, College Park, Maryland.
Guillermo Wibmer, Tallahassee, Florida.
In addition, there are specimens in the Henry and Anne Howden
collection. Types in our collection are deposited on loan in the
Canadian National Collection, Biosystematics Research Institute,
Ottawa.
All types were examined, and lectotypes were selected where
appropriate.
Old museum specimens are often not duplicated in modern material.
In this genus where some species appear to be rare - at least in
collections - locality data are often very helpful and internal parts
are sometimes essential for identification. When the old specimens
have the setae destroyed by psocids and the internal parts consumed by
dermestids and psocids, when the locality is incorrect, or incomplete
or absent entirely, and when there are no modern specimens that match
them, the taxonomist must decide if it is better to ignore the old
specimens or include them in the study. In the interest of
completeness, I have attempted to include such faulty material in this
revision.
Howden: Hadromeropsis 5
METHODS AND TERMINOLOGY
Species related by apparent synapomorphies are assembled into
groups. No nomenclatural status is intended for these groups. The
Characteristics of a group are not repeated in species descriptions
except to qualify them.
The Diagnosis gives the optimum number of characteristics which
distinguish a species within the species group.
Where described species are represented by fewer’ than 10
specimens, all the information on labels, sex, and collection are
given for each specimen. This information is summarized for described
species represented by longer series.
Previous authors have used various terms to describe the
Characteristics of the scales of Hadromeropsis. I have used
"scintillating," "iridescent," and “metallic lustre" which I
distinguish as follows. Scintillating scales are very smooth and
flat, like discs of thin metal, uniform in color but each with
brilliant green, gold and red reflections. Such scales leave only a
faint, pin-prick scar or a marginal scar as well as the central hole
and are more easily abraded than iridescent scales. They are found on
scintillans, gemmifer, dejeanii, etc.
Iridescent scales are flecked with multiple colors like the iris
of the eye or like an opal and may be slightly convex or at least have
the edges deflected. Iridescent scales are basically green, blue or
white and may be strongly metallic or not. The scar of an iridescent
scale consists of the outer perimeter as well as the central hole.
Iridescent scales are charactertistic of fulgens, Opalinus, etc. The
scales of species in the nominate subgenus can be distinctly
Categorized as iridescent or scintillating; these distinctions break
down in Hadrorestes and in the species earinus.
A metallic lustre that is not visible with a microscope but is
visible macroscopically in a glancing light may be present on species
with iridescent scales as in brevicomus, or non-iridescent scales as
in nobilitatus and fasciatus.
Setae are of several diverse forms. On the sides of the elytra
and the tibiae some species groups may have stiff, dark wiry setae.
In the opalinus and scintillans groups there are erect setae on the
dorsal surface. The characteristics of these erect setae are evident
only on specimens in very good condition because the setae are prone
to matting and the delicate filamentous tips break off readily leaving
no obvious evidence of having been there. Shorter and arcuate setae
are less vulnerable.
Another type of seta which I refer to as "long, wispy" is
particularly noticeable on the prosternum and inner surface of the
fore legs and is more highly developed in males than females. A
Similar but probably not analagous, long, wispy seta occurs often on
the base of the elytra and prothorax. Such a "wispy" seta is pale,
crinkled, and filamentous apically; when the tip is accidentally
broken off, the remaining base resembles an ordinary erect seta.
These setae seem to be associated with species with a waxy coating on
the dorsum as in many Hadrorestes species. This wax conceals details
of the sculpture and vestiture. It can be removed by gently stroking
the surface with a fine camel hair brush dipped in ammonia solution to
6 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
soften the wax and then further stroking with the brush frequently
rinsed in water to remove the globs of wax. This can be tedious but
often completely restores the color of the scales and position of
setae without matting as can happen in an ultrasonic cleaner. See
incompletely cleaned prothorax in Fig. 239, uncleaned surface in Fig.
The "interantennal line" is a transverse line across the dorsum of
the rostrum approximately opposite the insertion of the antennae. In
Hadromeropsis it is usually unmarked.
The relative length of the segments in the funicle and antennal
club are difficult to assess uniformly and have not been used in the
descriptions unless they are extreme.
The elytra in most species are approximately 2x longer than their
width at the humeri. This measurement is not given in_- the
descriptions unless it differs by more than 0.2x.
Where the tibia rests against the femur the surface of the femur
may be slightly smoother and concave (Fig. 257). This is referred to
as the "tibial groove," although a groove is not present in many
species. The contiguous edges of the tibia and femur are referred to
as the "inner edge" and the opposite surface is referred to as the
"outer" (Fig. 209). The remaining surfaces are referred to as
anterior (Fig. 258) and posterior (Fig. 257) as they are when the leg
is held at right angles to the body.
The "distal tooth" refers to the elongation of the extreme inner
apical angle of the fore tibia. According to the species, the distal
tooth provides many useful characteristics, ranging from short to long
and curved, and from simple to divided into two.
To dissect the genitalia, the abdomen was usually removed from the
beetle and the contents were treated with hot KOH. In the few cases
where specimens recently killed in ethyl acetate were available, no
treatment was necessary. For specimens dead several weeks, hot water
with a bit of detergent was sufficient treatment before extracting the
internal sac. On the other hand, many specimens of the argentinensis
and nobilitatus groups were never’ softened sufficiently for
Satisfactory dissections of the male or female genitalia. In these
cases I suspect the specimens had been collected or stored in formalin
or alcohol which so hardened the tissues that they did not respond to
rigorous KOH treatment. After extraction of the genitalia, the
abdomen was glued to a paper point on the same pin as the beetle and
the contents put in glycerin in a microvial on the same pin.
The aedeagus is relatively conservative in characters. Although
it is a heavily sclerotized structure, its dorsum may appear slightly
flattened or sunken in dried specimens compared to specimens in
glycerin. This is not apparent in the lateral view I used for
illustrations.
The internal sac was dissected from every species where it was
possible to do so, except species where a flagellum was obviously
extending from both ends of the aedeagus. The best technique was to
insert a fine, hooked pin a short distance into the apical orifice of
the aedeagus in very soft condition. Care was necessary to keep the
parts soft with a drop of water during the dissection. Repeated short
pulls were more satisfactory than a single deep effort, especially
when working with a curved aedeagus. After dissection the internal
Howden: Hadromeropsis 7
sac often distended naturally after a day or so in glycerin.
Sometimes an air bubble captured in the sac could be manipulated into
the various lobes to inflate them.
Because of their extremely long genitalia, males suspected of
belonging to the Mexican species flagellatus and dejeanii require a
different dissection technique. The most successful dissections of
old, dry specimens were obtained by the following procedure: keep
specimen in humidor for 12 to 24 hours; lift left elytron and wing out
of the way; with razor blade or scalpel slit the metathorax
longitudinally to the left of the median line and across to the side;
slit or cut integument of abdominal terga at extreme side nearly to
apex; with fine brush apply drop of ammonia or warm water to tissues
within integument until softened; observe position of genitalia and
lift out, or remove entire abdomen after freeing proximal end of
genitalia. :
Measuring the spermathecal duct is a delicate operation.
Measurements of the duct given here should be considered close
estimates instead of exact measurements.
Areas of the spermatheca are referred to as in Howden (1976:7-8).
The junction of the spermathecal duct with the body of the spermatheca
is the nodulus; the junction of the gland with the spermatheca is the
ramus; and the apex is the cornu. See Fig. 130.
MORPHOLOGY OF THE MALE AND FEMALE GENITALIA
Three rather distinct types of male and female genitalia are found
in the genus. Each type of male genitalia corresponds to an equally
distinct type of female genitalia. It is thus possible to examine one
sex of a species and predict some characteristics of the genitalia of
the other sex.
The genitalia of both sexes are known for only 36 of the 52
species (70%), and there are some anomalies that cannot be explained
until both sexes of all species are known. This must be remembered in
the following discussion which is based on these incomplete data.
Description of the Types of Genitalia
The first type of genitalia is found in the nobilitatus and
argentinensis groups of the nominate subgenus. In the male genitalia
of these groups (Figs. 159-180), the internal sac of the aedeagus when
everted is seen to consist of a membranous tube with various patches
of spicules and inflatable lobes on the proximal portion; a heavily
sclerotized internal structure toward the distal end; a dorsal,
inflatable, cupped, membranous lobe externally; the whole sac
terminating distally in a_= slightly deflected membranous’ tube
spiculate on the sides but with only a very fine, smooth membrane at
the apex. In dorsal or ventral view the internal sclerite* is shaped
* The proximal end of the internal sclerite is always concealed by
membranes, and I was never able to satisfy myself whether one or two
sclerites (fused or movable) are involved.
8 Contrib. Amer, Ent. Inst., vol. 19, no. 6, 1982
proximally like a condyle, i.e., like the end of a vertebrate femora]
bone; in lateral view, as I have drawn them, this is not particularly
evident. Good specific characters are found in the position of the
lobes as well as in the additional sclerotization of the distal
deflected portion.
Females of the nobilitatus and argentinensis groups (Figs.
181-183, 187-190) have a large complex sclerite within the bursa
copulatrix, sometimes almost filling the bursa. This sclerite is
basically funnel shaped with fins and appears very different at
various angles (Figs. 188-190). The vagina (or genital chamber)
(Figs. 182, 188) is faintly testaceous and has vaguely sclerotized
longitudinal streaks or flat rods its entire length. The spermathecal
duct is moderate in length. Below the distal end of the common
oviduct is an inflatable membranous cupped lobe.
The second type of genitalia is exhibited in the remaining H.
Hadromeropsis: the gemmifer, scintillans, and opalinus groups. In the
males of these groups the internal sclerite is elongated into a
flagellum of various lengths (Figs. 73-108), in its extreme
development longer than the beetle itself. The proximal end of the
flagellum is always. stiff and in extreme forms, such as flagellatus,
forms a large loop or figure 8 in the mesothorax (Fig. 80). The
length of the flagellum is species specific. In addition, the
manubrium of the spiculum “gastrale, the aedeagal apodemes, and the
tegminal strut may be individually or collectively elongated. The
relative length of these rods is also species specific. The tegmen is
much wider in species with a longer flagellum (Figs. 73, 75, 78). The
ejaculatory duct ends distally (the gonopore) in a membrane encasing
the proximal end of the ventral portion of the internal sclerite.
This junction is readily visible at the anterior end of the aedeagus
in species with the flagellum longer than the aedeagus.
The male genitalia of gemmifer (Figs. 101-103) are extreme with
only a minute, free, needle-like sclerite representing the flagellum.
There is also a sclerite on the ventral surface of a sort of dorsal
cupped flap. In dorsal and ventral views these two sclerites are very
similar in shape to the proximal end of a flagellum. The dorsal
cupped lobe of gemmifer seems to be homologous with the dorsal
inflatable cupped lobe of the argentinensis and nobilitatus groups.
With this in mind, and in view of the location of the gonopore in
gemmi fer (Fig. 102), it seems possible that the gonopore in the
argentinensis and nobilitatus groups is immediately beneath the dorsal
inflatable cupped lobe that is located over the proximal end of the
internal sclerites, but I was not able to establish this. If this is
the case, the large ventral inflatable lobe of gemmifer could be
comparable to the apex of the internal sac of the argentinensis and
nobilitatus groups.
In females of the flagellate species there is no sclerite in the
bursa copulatrix, nor any sclerotization of the vagina. The length of
the spermathecal duct is proportionate to the length of the flagellum
and is species specific*. The basic or unmodified length of the
Spermathecal duct is 1-1.5 mm in the nominate subgenus.
* This is not unique to Hadromeropsis. Thompson (1977:196) showed
(next page)
Howden: Hadromeropsis 9
In the new subgenus’ Hadrorestes, an abruptly = different
modification of the apex of the internal sac and a gradual change in
the internal sclerites constitute the third type of male genitalia.
In the alacer group (Figs. 310-316) the internal sclerite is
condyle-shaped proximally as in the argentinensis and nobilitatus
groups of the nominate subgenus, but the distal end of the internal
sac instead of being a thin membrane is sclerotized in the form of a
short, slightly spiculate tube which is always curved and directed
ventrad. The membranous parts of the internal sac are usually only
faintly spiculate. The genitalia of exilis (Fig. 366) resembles that
of the alacer group, but the sclerotized distal end is straight and
directed distad, the membranous tube is simple and has two distinct
patches of spicules, and the proximal end of the internal sclerite is
evanescent and not condyle-shaped. In impressicollis (the only male
representative of its group of four species) the sclerotized distal
end of the internal sac is almost straight and directed distad; the
condyle-shaped proximal end of the internal sclerite has a small
dorsal elongation (Figs. 317, 319). In the remainder of Hadrorestes
(Figs. 320-334) the internal sclerite at the proximal end is. enlarged
and acutely angled, and the distal end of the internal sac is finely
Spiculate, at least moderately sclerotized, curved, and directed
dorsad.
Females of Hadrorestes (Figs. 336-348, 350-357) have no
sclerotization in the vagina and inside the bursa have no complex
funnel-shaped structure, but there may be a small, faint cup, ring,
arc, or plate at the junction of the spermathecal duct. The ventral
inflatable cupped pouch is larger and tougher than in the other
groups; the ends of this inflatable pouch are attached to a pair of
lateral sclerites, and this constitutes the third type of female
genitalia. The caudal end of the common oviduct was occasionally seen
to also be connected to the lateral sclerites. To study the female
genitalia more thoroughly, it would be necessary to stain them. These
lateral sclerites are somewhat variable in size and_— shape
intraspecifically; they are absent in cavifrons (male unknown) and are
presumed to be secondarily lost in that species.
Intraspecific Variation in Genitalia
Variation in the genitalia is incorporated in the species
descriptions and remarks, but the following female parts warrant
Special note.
The spermatheca varies greatly in some species. Four examples of
the spermatheca of nobilitatus are shown in Figs. 191-194. Three
examples of variation in the spermatheca of excubitor are shown in
Figs. 196-198.
that in Apirocalus (Otiorhynchinae, Celeuthetini) the length of the
flagellum was reflected in the length of the spermathecal duct of the
females". Sharp (1918: P1.1X, fig. 7; 1920:76). made similar
observations on Celeuthetini.
10 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
allotype (Fig. 357) is highly modified, but the only female paratype
of this species has a normally slender duct. See Remarks on the
species.
The lateral sclerites of the vagina of Hadrorestes vary in detail
intraspecifically, as noted in previous section. Two examples of the
lateral sclerite of one species are shown in Fig. 354,
In the subgenus Hadrorestes where a distinctive bursal sclerite is
apparently not indicated by the morphology of the male genitalia, the
bursal sclerite is variable in development intraspecifically. An
extreme example is cavifrons where a large disc is present in the
bursa copulatrix of one specimen but absent in the other.
In H. (Hadrorestes) spiculatus the spermathecal duct of the
Interpretations of Male and Female Genitalia
The implications of the morphology of the corresponding male and
female genitalia are: a) in the flagellate species the flagellum
enters the spermathecal duct which is an appropriate corresponding
length; this would bring the gonopore into close proximity with the
bursa; b) in Hadrorestes the tough, strongly supported pouch below
the common oviduct accomodates either the dorsal spiculate lobe or the
acutely angled internal sclerite, anchoring it while the distal end
enters the bursa copulatrix; this would bring the gonopore into close
proximity with the spermathecal duct in the bursa; c) in the
nobilitatus and argentinensis groups, the faintly sclerotized vagina
withstands the heavily spiculate proximal portion of the internal sac,
the cupped lobe beneath the common oviduct does not need the extra
reinforcement provided by lateral sclerites to receive the dorsal
cupped lobe of the internal sac, and the funnel-like receptacle within
the bursa copulatrix is of an appropriate design for the _ broad,
expandable spiculate sides of the distal extension of the internal
sac.
Thus, if the gonopore must be brought into proximity with the
Spermathecal duct in the bursa copulatrix to effect fertilization,
then the morphology of the genitalia gives visual evidence of a
possible reproductive isolating mechanism. At the very least the
morphology of the male and female genitalia of Hadromeropsis has
proved to be very useful in associating the sexes of dimorphic species
as well as in relating species sometimes represented by only one sex
when the external properties of those species are variable and
sexually dimorphic.
BIOLOGY
The 15 species of Hadromeropsis which colleagues and I have
collected and observed were all diurnal. Three species are
brachypterous, but of the fully winged species at least superbus,
alacer, and pectinatus were observed to be strong, fast fliers.
Many species in the nominate subgenus were taken on trees or
shrubs of species of Leguminoseae, but not exclusively. Species in
the subgenus Hadrorestes, which occurs in the Andes outside the range
of most of these Leguminoseae, were taken on alder, grass, bamboo, and
Howden: Hadromeropsis re
miscellaneous unidentified plants. There was evidence of adult food
preference but not of specificity.
It is presumed the larvae are general root feeders. Bruch
(Hayward, 1960:18) reports the larvae of argentinensis attacking "los
espinelles" (Acacia caven (Mol.) and Mimosa scabrella Benth.).
There was physical evidence of predation on eight specimens of
Hadrorestes but in only six specimens of the much more common nominate
subgenus. Possibly the species with thinner integument or slower
movements were consumed outright by the predator whereas the very hard
or faster species escaped with only a cracked or nipped elytron. See
Remarks under Hadrorestes.
Genus Hadromeropsis Pierce
Hadromerus Schoenherr, 1834:127. Type-species Hadromerus nobilitatus
Gyllenhal, in Schoenherr, 1834:128, by original designation.
Hadromeropsis Pierce, 1913:400. Replacement name for Hadromerus
Schoenherr, 1834, nec Hadromerus Schoenherr, 1823.
Diagnosis.-Small to large, 5 to 20 mm in length. Scales never
sculptured. Posterior margin of epistoma never carinate or keeled,
although margin elevated distally in a few species. Mandible with
vestiture of lateral and ventral surface similar to that of rostrum.
Pronotum never produced anteriorly over vertex. Female with caudal
surface of ventrites 2, 3, and 4 conspicuously elevated, often
perpendicular or slanted anteriorly or posteriorly, edge of caudal
surface usually sharply delimited; character less developed in male.
Description.-Glabrous, squamose, or with both squamose and
glabrous areas arranged in a pattern. Scales with or without metallic
lustre, in many species strongly iridescent or scintillating. In
lateral view ventral surface of rostrum almost as long as dorsal
surface. Rostrum with interantennal line faintly marked at most.
Scar of mandibular cusp not situated on a process of the mandible.
Anterior constriction of prothorax absent dorsally in most species.
Fore leg larger than other legs; fore femur of male often greatly
enlarged (1.3-2.7x wider than hind femur) and often with a flange on
inner edge distally, flange situated anterior to tibial groove,
surface posterior to tibial groove at most weakly modified; fore femur
of female less modified. Fore coxae narrowly separated, the
separation sometimes concealed by the convex inner surface of coxae.
Hind tibia with corbel_ open. Inner surface of elytra with
well-developed apical carina between suture at end of interlocking
flange and side at apex of epipleural fold. Last tergite of male
simple.
Remarks.-The larger size, smooth scales, and presence of scales on
the mandible distinguish Hadromeropsis from Pandeleteius which is
probably the most closely related New World genus. Airosimus Howden
differs from Hadromeropsis in the presence of a "platform" on the apex
of the rostrum, the ventral surface of rostrum much shorter than the
dorsal surface, and the hind corbels semi-enclosed. The South
American aL DE Schoenherr is the only other New World Tanymecini
with which Hadromeropsis might be confused. pacropterue has a thin
integument, extremely elongate elytra and ventrites 1 and 2, and lacks
12 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
the apical carina on the inner surface of the elytra.
The African Hadromerus differs from Hadromeropsis in the following
Characters: mandibular scar situated on a process of the mandible;
prothorax with basal constriction adjacent to the perpendicular
margin; elytra very narrow across base which is perpendicular and has
the edge carinate. Hadromerus shares the following characters with
Pandeleteius but not with Hadromeropsis: scales sculptured; inner edge
of fore femur in some species distally modified with spur or teeth on
posterior side of tibial groove; last tergite of male variously
modified with carina or concavity.
The antennal scape of Hadromeropsis reaches the eye or exceeds it
(especially in the subgenus Hadrorestes) but does not reach the
prothorax (except striatus). The length of the scape is useful in
field recognition of similarly sized species of Naupactini with
enlarged fore legs, such as Naupactus and Macrostylus.
Three brachypterous species of Hadromeropsis are described from
uniques, two from males and one from a female. The proportions of the
elytra and prothorax look wrong for the genus, but this is a
consequence of brachyptery. In all three the wing is only 0.6-0.7x as
long as the elytra, the elytra are very narrow across the humeri, the
apical umbone is absent (elytra flat at the apical termination of
Striae 4-6), and the mesepimeron is very narrow.
The spiculum gastrale and the spiculum ventrale are conservative
in form and only one example of each is figured in Figs. 111 and 349
respectively.
In some males I observed a pair of very small sclerites (Fig. 109)
set on a flexible stalk arising from the first connecting membrane
between the spiculum gastrale and the 8th sternites. These sclerites
are apparently the same as "spicule plates", sensu Gilbert (1952:636;
Clark, 1977:105). The sclerites were very similar in all species but
not all were surveyed for this character.
All species examined have a rectal ring (Fig. 172).
The gender of Hadromeropsis is masculine since the ending "“opsis"
is adjectival and modi fies the masculine noun’ "Hadromerus."
Key to the Species of Hadromeropsis
ith DOGG T ING Cour Aiericar iy. Wee TOES PRR Nee,
Occurring in Panama and northward. Yo. Lo ee es a
as Eye flattened, scarcely exceeding outline of head.
Prothorax in dorsal outline strongly rounded on
Sides, much wider than long (Fig. 2). Elytra
clothed with patches of flat, imbricate, green
or lavender scales alternating with irregularly
placed rectangular glabrous areas. Length 7.5-
9.5 mm. Argentina. ........ . 13. superbus (Heller)
Eye convex. Prothorax with sides less strongly
rounded: cE Tytra not? so: patternieda Ys eo Te ey 88
3(2) Eye small (Fig. 289). Pronotum (Fig. 290) flattened,
surface irregularly sculptured. Base of elytra
4(3)
6(5)
7(4)
8(7)
between
Howden: Hadromeropsis
Striae 5 abruptly perpendicular and
slightly anteriorly produced. Male unknown.
Length
1S Ways VE CHAGOO Nans “Hisokiad Shs 51. earinus n.
Eye larger. Pronotum not so sculptured. Base
OF - Oly a. PounCed., 4. Kran sia Hin hel OP Be oe wk
Brachypterous, wing only 0.6-0.7x length of
elytron
Elytra
apical
. Mesepimeron very slender (Fig. 226).
without apical umbone, i.e., flat at
termination.of. striae: 4 to By scqoalwsti « ses
Wing much longer than elytron. Mesepimeron
normal
distinc
Elytra wi
Striae
large.
Elytra wi
indisti
Elytra wi
smooth,
tuberc]
green s
Elytra an
tuberc]
seta-li
unknown
Dorsal su
one col
shiny,
between
(Fig. 225). Elytra usually with
C OpAGG + UNDONE iat 6? a 3! Ae shee Ki wartangae te «
th intervals conspicuously convex;
distinct, straight, strial punctures
Female unknown. Colombia... 52. striatus n.
th intervals not convex; striae
nct or confused, strial punctures small. ....
thout tubercles. Disc of prothorax
sides of prothorax with obsolete
es. Clothed with large scintillating
cales. Female unknown. Bolivia . 32. exilis n.
d prothorax with crowded, small, uniform
es. Clothed with small white setae and
ke scales. Male unknown. Locality
5 ay Rg oe ae Ey egg . .36. brachypterus n.
rface densely clothed with scales of
or, the only pattern (if any) formed by
bare areas confined to elytral intervals
distinct striae, forming random dark
spots; or if entirely glabrous (some
gemmifer) with distinct tubercle on fore
coxa.
Elytral
Vestiture of male like that of female.
margin always smooth around ventrite
5. Many species with a tubercle on inner
distal
(Figs.
Dorsal su
edge of fore coxa opposite trochanter
Rie: CAG rte ys Sewanee arin” §
rface glabrous or squamose. If
Clothed with scales of one color, then usually
striae
not evident or bare areas forming a
fasciate or other pattern. Males often
glabrou
ently.
S, females squamose or colored differ-
Elytral margins smooth, tuberculate,
or denticulate around ventrite 5. Never with
a coxal
TUDONCTO. Gerace d’ 4AeSe Sve
Rostrum relatively long and narrow, 1.4-1.6x
longer
than wide (Fig. 63). Male fore femur
at distal end with ventral margin expanded
into a
green.
flange (Fig. 65). Scintillating
Bolivia (Pando), Brazil (Amazonas, Paré4),
13
Sp.
Sp.
Sp.
Sp.
12
14
10(9)
11(10)
12(7)
13 (12)
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
PPh ae bd Vibes Elana ge gt Pe 16. batesi n. sp.
Rostrum moderate in width and length, usually
less than 1.2x longer than wide (Figs. 55,
56). Male fore femur unmodified distally.
SCamenllatine.greemor NObts eye Veer eS oar ks. ca Se 9
Prothorax in dorsal outline strongly rounded
on sides, much wider than long (Fig. 49).
Unicolorous white (mature specimens) or
Slightly yellowed (teneral specimens).
Length. Ll-144 mm ieeBolivial 4 esc’. 10. aureus (Blanchard)
Prothorax in dorsal outline not strongly
rounded on sides. Seldomuwhites’. tse Aces 28 woe, 10
Anterior edge of rostrum at margin of epistoma
produced upwards and outwards (Fig. 156).
Elytral interval 9 with the glabrous spots
tuberculate. Fore tibia in end view (Fig. 154)
with a ventral lobe as long as the distal
LOOEH A BVArT Finis ee. eS Ee 23. beverlyae n. sp.
Anterior edge of rostrum not produced. Elytral.
interval 9 with glabrous spots not elevated.
Fore tibia in end view with ventral lobe
absent or much smaller than the distal tooth. ..... ie
Female with apex of ventrite 5 emarginate
(Fig. 59). Aedeagus longer, 3.1-4.2 mm, with
a short endophallic structure (Figs. 101, 102).
Elytra of male with sides tapering from humeri.
With a glabrous black form (mostly males).
Guatemala to northern Colombia and northern
Venezwelateid® 6.40 Se bc abs 14. gemmifer (Boheman), in part
Female with apex of ventrite 5 rounded (Fig. 60).
Aedeagus shorter, 2.4-3.0 mm, with flagellum
as long as aedeagus (Figs. 104, 105). Elytra
of male with sides not tapered from humeri.
Colombia (Cundinamarca, Tolima) . . . 15. meridianus n. sp.
Striae 9 and 10 contiguous, confused or otherwise
indistinct beneath apical umbone; if condition
uncertain, then with long, wispy setae across
base of elytra and usually with tubercles or
denticles around apex of elytra. Occurring in
the Andes, including the Sierra Nevada de Santa
Nav Gare Based gece ae Oia S subgenus Hadrorestes .. 23
Striae 9 and 10 separated, distinct beneath
apical umbone; never with long, wispy setae
on base of elytra, only fasciatus with
distinct tubercles around apex of elytra.
Occurring in South America other than in the
ANGGS Cee ee he ee eee, EU eee ee gg gg 13
Epistoma wider than long, occupying approximately
14 (13)
15(14)
16(15)
Howden: Hadromeropsis
0.5 of anterior edge of rostrum (Fig. 149).
Size small, length 5.0-8.0 mm. Strial
punctures often foveate, (adi cliies. A male.
b5
Brazdl. dines sGeVais jc. <<. 01 «dace te ulverulentus n.
ranger
Epistoma as wide as or (more eh ae
than wide, occupying 0.2-0.4 of anterior edge
of rostrum. Length 4.5-16.5 mm. Strial
PUNCTURES UNOG. TONGA TG. music weeps tetas ol meee ba s
Edge of elytra around ventrite 5 with distinct
acute setiferous tubercles when viewed from
above (Fig. 157). Fore femur without distal
flange. Rostrum of female with distinct
pterygia (Fig. 158), apex of rostrum also
produced slightly in a flange on either side
of epistoma, epistoma thus long and narrow and
anterior edge of rostrum bisinuate. Elytra
with a complete postmedian dark fascia (Fig. 27),
very conspicuous in female and often appearing to
be composed of three contiguous diamonds; male
with blue or green scales, fascia weak, outlined
in white. Length 9.2-16.5 mm. Southeastern
CVG, 11a: sccua Bbbaes Peas aid ls icsiencocrars «Gales eas, coat ZL wtascaatas . (bucas)
Edge of elytra around ventrite 5 smooth when
viewed from above, or if appearing somewhat
tuberculate or crenulate, then without al]
ADOVE: MEME 1 NANG CHAVACEORS6ce0! & -oiseatinni® -s) Sl SRE
Fore femur with distinct (but very weak in some
females) distal flange when viewed from behind.
Elytra with tubercles on lateral intervals
usually distinct in dorsal view. With
metallic lustre of gold or red. Fore tibia
abruptly bowed inwardly at distal fourth (Fig. 1).
Fore femur without distal flange or swelling
above tibial groove when viewed from behind.
Elytra with or without tubercles on lateral
intervals. With or without a metallic lustre.
Fore tibia straight or slightly curved inwardly
CARLA IE iso dg winidu ca, as Retey 9 COM AO a ae Ts
Male with distal tooth of fore tibia as long as
width of tibia at apex. Female with distal
tooth of fore tibia single, 0.5x as long as
width of tibia. Apex of elytra of male
produced into a brief divergent tooth. Length
of male 7-8.6 mm, female 7.5-10.7 mm. South-
eastern Brazil and adjacent Argentina. .....
wo. at laude pennies . . 24, nobilitatus (Gyllenhal),
Male with distal tooth of fore tibia 0.5x as long
as width of tibia (Fig. 141). Female with a
pair of distal teeth on fore tibia, the most
distal tooth equal to or shorter than the
~ 16
in part
16 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
second (Fig. 142). Apex of elytra of male not
at all produced. Length of male 8.2-10.5 mm,
female 9.4-12.8 mm. Brazil (Rio de Janeiro,
Sanita Catan i nad oh eiud vient eh DRO ms GON 26. excubitor n. sp.
17(15) Large, length of male 9.5-11.4 mm; female
11-14.2 mm. Elytra without tubercles. Elytra
of female with anchor-shaped dark or glabrous
area (Fig. 13). Elytra of male green, blue, or
tan with pattern of female faintly marked with
white. Southeastern Brazil and Paraguay. . .
ghee aake tak ale MSGS AID kw ihee Vo 17. togatus (Boheman)
Smaller, length of male less than 9 mm, of female
less than 10.7 mm. Elytra with or without
tubercles, not patterned as above. ....... Coe 8 se
18(17) Dorso-lateral edges of rostrum poorly defined,
broadly rounded (Fig. 151). Argentina
(Misionés), Brazil (Minas Gerais), Paraguay,
nO ayers car aetee We ey Ae Gg Regs gm 21. pallidus n. s
Dorso-lateral edges of rostrum distinct. ........ ee
19(18) Elytra short and thick, convex in profile,
declivity almost perpendicular, apical umbone
absent (Figs. 7-10). Elytra with a large dark
postmedian spot on intervals 5, 6, and /; without
metallic lustre. Northern Argentina, Brazil
(Santa Catarina), Paraguay, Uruguay. .....
JO A aie BMY gv ML eae 18. argentinensis (Hustache)
Elytra not shaped as above. If elytra with a dark
postmedian spot, then also with either glabrous
tubercles on apical umbone or with a distinct
COLON VAIS Ghee ve Sian pe He AM ree! ie elie Se ees 20
20(19) Elytra with some glabrous setiferous tubercles on
apical umbone and usually on declivity and
lateral intervals as well. Without metallic
lustre. Color pattern similar to that of
argentinensis. Brazil (Parana, Santa
C ACA ING ph GeO, POU) ornate %, whet net ie” wel oltus 19. plebeius n. s
Elytra without distinct tubercles, but glabrous
Spots may be slightly convex. With or without
MG Dee Pree re I eh Mh ie pe BH Sw 8 8s 21
21(20) Female ventrite 4 with caudal margin straight in
ventral view, arcuate in caudal view (Fig. 143).
Elytra of male long and flat in profile. Fore
tibia almost straight, only weakly curved inward
distally (Fig. 140). Brazil (Minas Gerais),
Santa Catarina, S80 Paulo). ..... 22. speculifer n. sp.
Female ventrite 4 with caudal margin pointed
medially (Fig. 155). Elytra of male shorter,
more convex. Fore tibia distinctly bowed
Howden: Hadromeropsis 17
inward! Mista ligi (Pa gses iad Po lege oye, 2k. 22
22(21) With distinct golden lustre. Ventrite 5 of
female medially smooth and polished, without
scales. Southeastern Brazil and adjacent
Argentina?’ 6° P)9GRh.4 24. nobilitatus (Gyllenhal), in part
With metallic lustre absent or very faint.
Ventrite 5 of female with scales evenly
distributed or sparser medially (Fig. 155).
Brazd4-4Minas Geraisie ys oge Fie 25. atomarius (Boheman)
23(12) Scales when present very elongate, seta-like;
scutellum conspicuously clothed with dense white
elongate scales. Pronotum usually with a
shallow depression on each side and a median
COPVES STOW BS WETS a6 WE eee SIRE ee de a 24
Scales when present rounded in shape; scutellum
glabrous or variously clothed. Pronotum without
both a pair of lateral depressions and a median
depression (except some pectinatus).........e-. 26
24(23) Head and rostrum with a shagreened microsculpture
and scattered very fine punctures, the only
other sculpture being a frontal fovea (Fig. 222).
Ventrite 5 of female flat. Male unknown. Peru
LNuAnGGd)? g2..2 goa" 2499, G4 ee bc 35. bombycinus n. sp.
Head and rostrum not sculptured as above.
Ventrite 5 of female longitudinally convex
GP ICOIG a4 BEE Pees ALOR Reh eae tyes, tS 25
25(24) Female with elytra (Figs. 215, 218) abruptly
constricted beneath apical umbone, then flared
Outward in a prominent flange. Sculpture of
rostrum and frons consisting of short,
irregular rugae (Fig. 216). Male unknown.
ROURORPe ioe Sok Qisky ay sie? Paws oe 34. institulus n. sp.
Female with elytra (Fig. 214) gradually tapered
apically. Sculpture of rostrum and frons
around frontal fovea (Fig. 210). Colombia. . .
is ah ae ky eM RO a 33. impressicollis (Kirsch)
26(23) Rostrum with extreme hemispherical concavity
exaggerated by keeled dorso-lateral edges
(Figs. 282, 283). Size large, length 15.8-17.4
he PSH. See 4 Tn oa ak ale ae ae Toe ae 50. cavifrons n. sp.
Rostrum not so modified. Size small to large. ...... 27
27(26) Large, length 11-20 mm. Punctures of elytra not
aligned in striae and with many extra punctures
of the same size. Fore tarsus with segment 2
much wider distally, abruptly tapered proximally
(Figs, 302, 304, 306, 309). Eye separated from
18
28 (27)
29 (28)
30 (29)
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
anterior margin of prothorax by its own diameter
OY More “CNUs -FOrMing a STONE NECK see a ae 28
Smaller, length 7.6-16 mm. Punctures of elytra
arranged in straight striae, usually without
extra punctures. Fore tarsus with segment 2
narrower distally, gradually tapered (Figs. 305,
307, 308 an Eve closer fo.pyothoraxs wt fasaweisye es ¢ Sl
Pronotum slightly, evenly convex, without lateral
flattened or depressed area. Elytral punctures
very small in glabrous areas (Fig. 206). Gla-
brous specimens with vitta on lateral edge of
metasternum of dense, imbricate white scales.
Female with apex of elytra broadly rounded-
truncate; ventrite 5 with deep lateral fovea.
Sutural interval at summit of declivity without
long, erect setae in either sex. Colombia.
PPT AG os PE SIRS Re 31. silaceus n. Sp.
Pronotum with lateral flattened or depressed area.
Elytral punctures larger, sometimes foveate.
Glabrous specimens never with concentration of
scales along side of metasternum. Female with
apex of elytra slightly produced, sutural inter-
val attenuate into a brief tooth; ventrite 5
flat or convex laterally. Sutural interval at
summit of declivity with long erect setae in all
females and in males of alacer and inconscriptus ... . 29
Elytra sparsely (male) or more densely (female)
(Fig. 205) clothed with rounded white and pale
colored scales, both sexes with a vague post-
median "V" outlined in larger, paler scales;
some specimens with metallic green scales
ventrally. Female with, male without long erect
setae at summit of declivity. Colombia (Sierra
Nevada de Santa Marta) ..... . . 30. nebulicolus n. sp.
Elytra of male and sometimes female with only
minute scales, no pattern; appearing glabrous
to naked eye. Female and male with long erect
Setae at suimmity Of -deGl 1V1 tyaue?.ladanechene ere id o.. 30
Setae of disc of elytra conspicuous, 2x longer
than the diameter of a fovea (Fig. 204). Both
sexes with minute scales only. Spermatheca very
long and contorted, as in Fig. 339. Ls : :
BN RED Se aoe ah 8 inconscriptus n.
Setae of disc of elytra as long as hes ” tones
(Fig. 203). Both sexes with minute scales only
or female with larger ochraceous scales forming
a pattern with 1, 2, or 3 dark fasciae. Sperma-
theca as in Fig. 336. Colombia, northern
COU GOU te a Faden Ae dle £4 wee Ae ge ¢ Gh Ete . « 28. alacer n. sp.
s1{27)
o2(31)
go\31)
34 (33)
35 (34)
Howden: Hadromeropsis 19
Apical umbone of elytra prominent in dorsal
outline (Figs. 259, 260), set with acute
tubercles each bearing a short, curled seta.
Dorsal surface nowhere with long, wispy setae
or erect setae except at summit of declivity.
Black with sparse minute green scales or |
covered with full sized iridescent green
scales with a pattern of glabrous black
PasCiaess PCR eCOrt be ee a at eb aE 2 ek et a ee 32
Without all the above characteristics. Ecuador
OP BOEST Fe Bie eae et eae ee or a ene ee ah
Fore tibia (Fig. 258) almost cyclindrical,
smooth, nearly impunctate, with a few fine
recumbent pale setae. Fore tibia straight or
nearly so. Fore femur of male (Fig. 257)
enormously swollen, with tubercles
above and below tibial groove. . . . 43. conquisitus n. sp.
Fore tibia (Fig. 262) with confluent punctures
and rugulae, with numerous dark wiry hairs or
setae. Fore tibia distinctly bowed distally.
Fore femur of male with distal flange weak,
without tubercles except minute ones on
Plane ee ae es 8 LA Mane Cae as 44. scambus n. sp.
Prothorax (Fig. 266) with very uniform, rounded,
evenly distributed tubercles. Male: posterior
face of fore femur with 6 or more well-
developed shelf-like tubercles; fore tibia with
3 or more extremely long teeth (Fig. 267).
Female: caudal surface of ventrites 2, 3, and
4 "Yuguiose: {P4q./2692"270 )em. a? S04 42. pectinatus n. sp.
Prothoracic sculpture various, not as above. Male
with or without shelf-like tubercles on
posterior face of fore femur; teeth of fore
tibia smaller, more nearly uniform in size.
Female with caudal surface of ventrites 2, 3,
and 4 smooth and shiny (finely sculptured in
CORT ACLU SG ate et es eeu ee ee eee Oe ee hea 34
Pronotum broadly flattened (Figs. 271, 288). Base
Of @1y tra witn, ONG: Wisby Setaes -s . 8 oe ate Ree 4 35
Pronotum not broadly flattened, may be concave or
narrowly depressed along median line. Base of
elytra with or without long, wispy setae. ....... 36
Elytra long and slender, in male 2.2x longer than
width across humeri (Fig. 38), in female 2.4x
longer than width across humeri. Fore femur
of male 2.4x, of female 1.2-1.4x wider than
hind femur; distal flange distinct, its edge
GON Tau Tae et ee re ee ee eau 48. spiculatus n. sp.
Elytra shorter and broader in female (Fig. 31)
20
36 (34 )
37 (36 )
38 (37)
39 (38)
40 (39)
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
(male unknown), 2.2-2.3x longer than width
across humeri. Fore femur 1.2x wider than
hind femur; distal flange obsolete, not
CONC COU Abe she Gee AO cee bak 49. picchuensis n. $s
MateS eS Shh As Van ee Cheah og a ae Ge 37
PORGASS 2. Thi RRA a ee SOR NO SET ON Gee Rawiwne 6 % oe 4 42
Posterior face of fore femur with shelf-like
tubercles. Basal third of elytral interval
10 with setiferous tubercles approximately as
large as the punctures of adjacent striae 9
and 10. Posterior half of hind coxa covered
with rounded scales. Venezuela. . ....-.+ «es
Vee weir te pee 40. dialeucus n. sp., in part
Posterior face of fore femur smooth, without
tubercles. Basal third of elytral interval
10 smooth or almost, setae arising from smooth
surface, punctures on basal third of striae 9
and 10 often large or even foveate. Hind
coxa with some rounded scales or not. ..... Sonera aw
Disc of elytra smooth and polished, with large
white scales densely clustered to form three
spots (Fig. 36). Mesepisternum densely
covered with large white scales (prone to
abrasion). Elytral interval 10 opposite
metasternum wider than adjacent interval 9
(Fig. 251). Colombia... . 45. magicus (Pascoe), in part
Disc of elytra with minute scales assembled in
brief, transverse depressions (depressions
present whether scales abraded or not);
without large scales. Elytral interval 10
Opposite metasternum not conspicuously wider
than adjacent interval 9 except briefly in
MANATDULAE TS: “Sorat seh eiuhan shot sal tGee eek Se. 5 BY
Small, length 7.6 mm. Fore femur very slender,
as wide as rostrum. Pronotum (Fig. 238) with
iatnbe impressed median line. Ecuador. ........
argon, length 8.5-11.7 mm. Fore femur enlarged,
0.3 or more wider than dorsum of rostrum. Pro-
notum with or without distinctly impressed
median Tins ows es ett wh daha WNT Gg ak ak cue San Ei care an |)
Pronotum (Fig. 234) with median line deeply,
broadly impressed, ending in distinct basal
and apical constrictions. Size smaller, 8.5-
£005 Gis, Cuadernos se) wi oeas CRANSENGINGS N.4sp., in part
Pronotum with median line unmarked, apical
constriction unmarked dorsally. Size larger,
OVER TED Ws Ale let te ae Make Boks oe ae Gr a ae 4]
41(40)
42 (36)
43 (42)
44 (43)
45 (44)
46 (45)
Howden: Hadromeropsis 21
Elytra in dorsal view with sides gradually tapered
from about middle to apex. Elytra in cross
section convex dorsally. Apices of elytra almost
vertical, only very briefly individually rounded
(igs 201 Ri oemowador Powe. Pes 46. nitidus n. sp., in part
Elytra in dorsal view with sides parallel or nearly
SO to apical umbone. Elytra in cross section
flattened dorsally. Apices of elytra oblique,
broadly individually rounded (Fig. 247).
COLGMD TAS Iw Old OS 47. mandibularis n. sp., in part
Mesepisternum with large, rounded white scales.
Elytra smooth and polished between conspicuous
white markings, interval 2 densely squamose
forming a vitta from base to summit of
decl ity 2° Gotonbia d+. fs ~ 45. magicus (Pascoe), in part
Mesepisternum never with large white scales.
Elytra variously patterned, never with a vitta
On “interve bee, @y5, Sg OP ety Be eds ee be, i's BO
Ventrite 5 (Fig. 278) with very deep lateral
depression. Ventrites 3, 4, and 5 much narrower
than ventrites 1 and 2; edges of elytra likewise
rather abruptly convergent (Figs. 37, 277). With
white fasciae on elytra. Bolivia. . 41. contractus n. sp.
Ventrite 5 with surface not depressed below
lateral edge. Ventrites 3, 4, and 5 gradually
narrowed to apex; edges of elytra gradually con-
vergent. Elytra with or without white markings. .... Aa
Dorsal outline of elytra serrulate from acute
tubercles of intervals 8 and 9, apical umbone,
and apex (Fig. 279). Posterior half of hind
coxa covered with rounded scales. Elytra with
minute white or blue scales in transverse
depressions, also usually marked with larger
white scales in a maximum pattern of basal
ring, median and apical fasciae (Fig. 28).
Venezuere me eR Serr: . - 40. dialeucus n. sp., in part
Dorsal outline of elytra serrulate on apical half
at most. Hind coxa without rounded scales.
Elytra NOt se patterned) ey aa ere LS, BP aa! ed
Elytra marked with two long, white, elliptical
loops. Elytra shorter, 3.6x longer than pro-
thorax,» Cole@ittwrpeccved,.: 4 46. nitidus(?) n. sp., in part
Elytra without white markings. Elytra longer,
3.8-4.0x longer than prothorax. Colombia,
ECU Oy cy ehh TR ge Oe MS Nal erage) Ra IE oy 46
-Pronotum medially not depressed, surface rather
smooth with punctures (Fig. 245). Mandible with
47(45)
48(1)
49 (48 )
50 (49)
51 (50)
52 (48)
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
deep, sharply defined transverse dorsal groove
(hoig.244). .bength 16.2 aims. Colombia. 2. ses.
o uacun Malte Cel cael le aes 47. mandibularis n. sp., in part
Pronotum medially depressed or flattened, median
line with transverse sculpture. Mandible with
dorsal setae not set in groove. Length 11.0-11.5 mm. . 47
Elytra with an aeneous lustre. In profile apex of
elytra dorsad of apical umbone. Occurring at
S200) Mis. EP CUGKOR SS). é extecnstes ice ol aster vk ihe 39. apicalis n. sp.
Elytra shiny black without metallic lustre. In
profile apex of elytra ventrad of apical umbone
(Figs. 231, 232). Occurring at 1500-2000 m.
E CUAMO I: cai here Ceimentehie Heirs 37. transandinus n. sp., in part
Fore tibia straight (Figs. 66-68). Scales irides-
cent or not, never scintillating (as defined
1H, IRCVOGUCTION) 4 ta Godke £504 tek ern er aeees 6. 49
Fore tibia curved inward distally (Figs. 69-72).
Scales Scie lating OF HOt. ok fees RA ee ek 52
Eye large and only feebly convex (Figs. 40, 42).
All dorsal setae both sexes erect, long, dense.
Mexico MM ichoatan) oh 3%. cin. Sse 3. crinitus n. sp.
Eye more convex. Setae of elytra erect; setae 0
prownoraX and Nead Grect OF NOL. ce: om wri) whiieliewe 2 6 \e 50
Very uniformly and densely clothed; scales of
elytra not overlapping; discrete or contiguous.
Glabrous spots not larger than one scale. Mexico
(MOVelOS TO CN1apaS).. «6.56 3 os. 2. fulgens (Champion)
Scales more irregularly distributed; scales of
elytra overlapping in some areas or with larger
G1 apyaus, drmeds or Both a. 2 S.. l S) ear Bethe 6 51
Fore femur without distal flange. Postocular
vibrissae lacking or very poorly developed.
Setae of head and prothorax not erect in either
sex. North of Tropic of Cancer in Mexico
(Durango, Sonora, and Zacatecas) and U.S.A.
CAR ZONG I ren Saiy areal sok ius aay toe lon Os ton fe 1. opalinus (Horn)
Fore femur with brief but distinct distal flange,
often with small shiny granules on edge of
flange. Postocular vibrissae moderate. Setae
Of head and prothorax erect in both sexes.
Mexico (central highlands). ..... 4. flagellatus n. sp.
Fore coxa with a tubercle on inner distal edge
Opposite trochanter (Figs. 57, 58). Prothorax
with low tubercles on sides. Ventrite 5 of
female distinctly notched at apex (Fig. 59).
Guatemala, to northern Colombia and northern
VENGZUCh Arerctl a: kG a his 14. gemmifer (Boheman), in part
BoA 52 }
54 (53)
55 (54)
56 (54 )
57 (56)
Howden: Hadromeropsis ao
Fore coxa without a tubercle on inner distal
edge. Prothorax usually without tubercles.
Ventrite > of female-roundede i.) PON a eG Frege Og
Densely clothed with imbricate pure white scales;
elytra with sparse (8-10 per interval) glabrous
spots not at all elevated and nowhere with
tubercles (Fig. 52). Base of elytra arcuate
between striae 5. Length 10.0-12.5 mm. Panama
(Chividatly Costa Rica... 29027 0oe 11. cretatus (Champion)
Usually clothed with scintillating or iridescent,
colored scales. If clothed with white scales
(occasional amoenus, brevicomus, dejeanii,
and scintillans), scales with some opalescence
Or iridescence under magnification. Base of
ely trausuat ly Stra rant. Oe eee ee ee See te RG 2 eae
Female over 13 mm in length (male unknown). Costa
Rica... Guavemasa. Ue .aie, Ee St ee ok 55
Female usually less than 10 mm in length, male
Under Tal) WNL OSes ae eee Ue ee, ARES ee Pe 56
Ventrite 5 flat, glabrous medially. Elytra with
a vitta on interval 4 from base to summit of
declivity and a vitta on interval 8 continuous
with one on prothorax; vittae formed of larger,
Overlapping scales. Costa Rica. . . 12. rufipes (Champion)
Ventrite 5 convex, evenly squamose. Scales of
elytra all of one size, not forming a pattern,
except of random glabrous spots gradually dimin-
ishing In ’size from base’to apex?” Guatemalal eos. . 2S".
Le IEE AMT PRS IES IG rere ity: et, PON, 8. micans (Champion)
(Examination of genitalia may be necessary for
positive identification of next four species).
Setae of disc of prothorax both sexes short (as
long as 1-1.5 scales), appressed. Elytra
Shorter; in male 2.5-2./x longer than prothorax,
in female 2.8-3.2x longer than prothorax. .... eS: SBF
Setae of prothorax both sexes longer (as long as
1.5-6.0 scales), not appressed, usually erect.
Elytra longer; in male 2.7-3.1x longer than
prothorax, in female 3.1-3./x longer than
PROLHORAKIT MIRO Rg ER RE TRUS Aue ty, Sas een 58
Scales scintillating green, sometimes with irides-
cent scales interspersed. Elytral glabrous areas
evenly distributed. Mexico, usually north of
Isthmus of Tehuantepec. ...... . 5. dejeanii (Boheman)
Scales iridescent green, often with golden or
coppery sheen in reflected light, or white (one
female). Elytral glabrous areas largest on inter-
vals 1, 2, and 3, often coalescing to form short,
24 Contrib. Amer. Ents«hosta) vols .29, no. 6, 1982
sinuous fasciae. Mexico (Chiapas) . . 9. brevicomus n. sp.
58(56) Flagellum shorter than aedeagus, 1.3-2.0 mm long
(Figs. 84-86). Spermathecal duct 1.5-2.1 mm
long. Occurring in Mexico north of Isthmus of
Penman bepecs qk at veh eae ae ee oe Oc vameenusin. sp.
Flagellum measured within aedeagus 4.1-6.0 mm
(Figs. 87-89). Spermathecal duct 4.3-7.0 mm.
Occurring in Guatemala and Mexico south of
Isthmus of Tehuantepec. .... . 7. scintillans (Champion)
Subgenus Hadromeropsis, new status
Hadromeropsis Pierce, 1913:400. Type-species, Hadromerus nobilitatus
Gyllenhal, by original designation.
Diagnosis.-Clothed with scales (except some gemmifer glabrous).
Color pattern of male similar to that of female or not. Prothorax
more or less evenly convex, never with depressions and elaborate
sculpture as in many Hadrorestes. Elytra with apical edge around
ventrite 5 smooth or weakly tuberculate (nobilitatus group). Striae 9
and 10 discrete, usually well-separated below apical umbone. Internal
sac of aedeagus in the form of a membranous tube with lobes and
patches of spicules on the surface and internally with sclerites; in
some groups membranous tube variously reduced and internal sclerites
in the form of a flagellum. Female never with paired sclerites in
vagina caudad of bursa copulatrix; spermatheca in one plane or nodulus
slightly angled (fasciatus).
Remarks.-The species assigned to this nominate subgenus. on
morphological characters occur from Arizona in the United States to
Argentina, and usually not in the Andes. Exceptions are aureus, which
occurs in semi-tropical mountain valleys of Bolivia at elevations up
to 1500 m, and two species of the gemmifer group, gemmifer and
meridianus, which occur in the Andes of Colombia and Venezuela at
elevations up to 1800 m. |
The opalinus Group
1. opalinus (Horn) 3. erinitus ‘hasp.
2. fulgens (Champion) 4. flagellatus n. sp.
Characteristics of Group.-Scales iridescent oor not, never
scintillating. Without a sharply defined color pattern. Without
tubercles or pustules on prothorax or elytra. Setae of elytra uniform
or of randomly varying lengths, not conspicuously longer on alternate
intervals. Fore femur with distal flange of inner edge weak to
moderate in flagellatus, weak or absent in others. Fore tibia
Straight (Figs. 66-68), distal tooth weak. Endophallic structure a
flagellum (but not known for crinitus); ring of tegmen wide (except
crinitus). Female genitalia without bursal sclerite; spermathecal
duct proportionate in length to that of flagellum.
Remarks.-These are the northernmost representatives of the genus,
Howden: Hadromeropsis 25
ranging from the Isthmus of Tehuantepec to Arizona.
In this group the flagellum reaches its maximum development
(flagellatus) and the postocular vibrissae their maximum reduction
(opalinus).
1. Hadromeropsis (Hadromeropsis) opalinus (Horn)
Figs. 39, 67, 74-76, 112, 153; Map 1
Hadromerus opalinus Horn, 1876:85. Champion, 1911:183. LECTOTYPE, HERE
DESIGNATED, male, labelled "Ariz. 49," "Type 326" (Cambridge).
See Type Material.
Hadromeropsis opalinus (Horn); Pierce, 1913:400.
Pandeleteius viridissimus Van Dyke, 1943:108. Type, female, labelled
Montezuma Pass, Huachuca Mountains, Arizona, VIII-19-1940," "Van
Dyke Collection", "Holotype No. 5342 Pandeletius virisissimus
[sic] Van Dyke" (San Francisco). Synonymized by Howden,
1959:419.
Diagnosis.-Clothed with blue, blue-green, green, white or coppery
scales; scales not scintillating, most not strongly iridescent.
Elytra often with an elongate pattern on intervals 2, 3, and 4 or 3,
4, and 5 formed of imbricate, slightly paler scales. Postocular
Vibrissae (Fig. 39) absent or very poorly developed (maximum length
0.3 mm). Setae of prothorax not erect in either sex, parallel to
surface but usually not touching it. Fore femur with distal flange
absent or obsolete. Apical edge of fore tibia (Fig. 67) with narrow,
acute lobe next to inner edge; lobe approximately as long as distal
tooth. Flagellum 4-4.5 mm long. Spermathecal duct 4.5-6 mm long.
Description.-Male, length 6.4-8.2 mm, width 2.3-3.0 mm. Female,
length 7.1-9.5 mm, width 2.8-3.8 mm. Color as in Diagnosis, the green
and blue occurring in 86% of the specimens, white, pinkish white and
coppery in 14%. Green or blue specimens with greenish or golden sheen
Or metallic lustre, others with or without rosy lustre. Prothorax
sometimes faintly vittate. Color of venter same color as dorsum or
infrequently pink in specimens which are green dorsally. Naturally
glabrous areas of prothorax and elytra irregular in size and
placement, ranging from the size of a scale to width of interval, a
variety of sizes present on any specimen. Rostrum flattened or
Slightly concave; dorso-lateral edges parallel or slightly divergent
basally; median line usually finely impressed and narrowly glabrous
from between eyes to interantennal line where it is often not
impressed, more broadly glabrous. Epistoma as long as wide, occupying
0.3 of anterior edge of rostrum; with 1 or more scales on epistoma in
6% of males, 3% of females, remainder without scales. Prothorax of
male averaging 1.1x, of female 1.2x wider than long; surface with some
fine punctures; tubercles or granules at most very weak, usually
absent. Postocular vibrissae as in Diagnosis. Setae of disc as long
as 2 (usually) or 3 scales, anteriorly directed, not erect; setae may
be perpendicular to surface on sides at basal and apical
constrictions. Elytra across humeri in male usually 1.2x, in female
1.3x wider than prothorax. Elytra of male 2.8-3.1x, of female
3.1-3.2x longer than prothorax. Humeral angles prominent. Sides of
elytra parallel or almost; apex of male rounded, without a_ tooth.
Apical edge of elytra often thickened both sexes. Female with apex
26 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Slightly attenuate or not beyond weak apical umbone, sutural interval
ending in a tooth no longer than 3 scales, usually much shorter.
Widest intervals of disc with 4-6 scales abreast. Setae of elytra
erect in both sexes, stiff, as long as 2-3 scales, uniform in length.
Female at summit of declivity on sutural interval with line of 4-6
elongate setae of increasing then decreasing size, the longest seta
2-2.5x longer than those of disc. Fore femur of male 1.5-2x, of
female 1.4-1.6x wider than hind femur, usually without a trace of
flange on inner edge. Fore tibia as in Diagnosis. Venter evenly
Squamose. Ventrite 5 of male 1.9x wider than long, flat to distinctly
convex, apex emarginate. Ventrite 5 of female flat or almost flat,
triangular with apex very narrowly rounded, averaging 1.6x wider than
long; scales sparser medially and apically in some. Male genitalia as
in Figs. /4-/6; aedeagus 2.4-2./ mm long, aedeagal apodeme 1.8 mm
long, tegminal strut 1.5-1.8 mm long, flagellum 4.0-4.5 mm _ long.
Spermatheca as in Fig. 112; spermathecal duct 4.5-6.0 mm long.
Type Material.-PARALECTOTYPES of Hadromerus opalinus, HERE
DESIGNATED, I male, 1 female: 1 male, Tabelled i {lors
"Lectotype 2830" on red paper, "Horn Coll, H 8313", "Hadromerus
Opalinus N" in pencil on white paper [Note: this specimen had been
isolated in the Academy of Natural Sciences, Philadelphia, collection
of types as the lectotype by a technician before the collection went
to the Museum of Comparative Zoology (J. Lawrence, in litt.); the
specimen is in very poor condition.] (Cambridge); 1 female, "Ariz,"
"5/1 73," "49," "169," "Type 326," "Hadromerus opalinus Horn" on white
paper ruled with pale blue lines (Cambridge).
Distribution.-Map 1. MEXICO. Durango: Canelas, Durango, 23 mi §S
Durango, 24 mi NE Durango, E1 Salto, 6 mi NE El Salto, 28 mi E E1
Salto, Navahos (20 mi E £1 Salto), La Ciudad, Francisco I. Madero,
Otinapa, Palos Colorados. Sonora: 6 mi NW Cananea. Zacatecas: 8 mi S
Fresnillo, 2/7 mi NW Fresnillo. UNITED STATES. Arizona: Canelo,
Chiricahua, Copper Canyon, Greaterville (Sta. Rita Mts.), Montezuma
Pass, Parker Canyon (Huachuca Mts.), Tex Canyon (Cochise County).
Specimens were collected in July and August.
Specimens examined: 108 males, 96 females. Specimens in Berlin,
Cambridge, London, New York, Ottawa, Sacramento, San Francisco,
Tucson, Howden, O'Brien. |
Remarks.-Of the 31 specimens in the British Museum labelled
Opalinus by Champion, only two are actually opalinus. Hence, the
escription and discussion of opalinus atfered by Champion
(1911:183-184) should be disregarded. He notes that he did not see an
example from Arizona, the type locality. The male illustrated by
Champion in Tab. 7, Fig. 29, is from Las Vigas, Veracruz; it is a
teneral specimen of flagellatus with the scales incompletely colored.
The specimen depicted in Fig. 30 is a teneral female labelled "Ciudad,
Mex., 8100 ft., Forrer." There is a male, also teneral, with
identical data to this female and these are the only two specimens of
opalinus in Champion's series. Champion refers to this locality as
"equdad in Durango" and not in the state of Mexico; Selander and
Vaurie (1962) place La Ciudad at 148 km WNW of Durango. This female
is robust and exceptionally large, 9.5 mm long, 0.5 mm longer than the
next largest female. The setae of the elytra are as long as about 4
scales, but the scales appear to be incompletely developed.
Howden: Hadromeropsis ad
Other specimens labelled opalinus by Champion are 6 scintillans
from Chiapas, 3 amoenus, 21 flagellatus (1 in Dresden).
In opalinus the postocular vibrissae and the femoral flange are
the least developed of any Hadromeropsis. This combined with the more
northern range are usually sufficient to recognize the species.
However, the single specimen from 2/7 mi NW Fresnillo has rather
well-developed postocular vibrissae; this specimen also differs from
typical opalinus in having the setae of alternate intervals of several
lengths, and the rostrum more concave. Since the spermathecal duct is
4.5 mm long and the spermatheca is within the range of variation of
opalinus, I presume that in this specimen the vibrissae are
exceptional.
Arizona specimens are less often patterned than those from Mexico.
Adults of opalinus seem to prefer Mimosoidea. A long series from
24 mi NE Durango (Aug. 20, O'Brien and Marshall) were taken on Acacia
schaffneri, and the Arizona specimens were often on Calliandra
eriophylla. Other plants recorded are Acacia sp., pine (one specimen)
and Ceanothus depressus.
Various Durango and Zacatecas localities are described by Spieth
(1950) in his account of the David Rockefeller Mexican Expedition of
the American Museum of Natural History.
2. Hadromeropsis (Hadromeropsis) fulgens (Champion)
Figs. 41, 46, 66, 73, 116; Map 1
Hadromerus/ fulgens “Champion, 1911:164, Tab. ’7,.. Figsso 32,.: 33.
LECTOTYPE, HERE DESIGNATED, male, labelled "Amula, Guerrero, 6000
fio, SOD. Hells colli thy 8... 2 Sh.0 i Guveu ls TR aoe ol, a> IN
pt. 3, Hadromerus fulgens, Ch." (London). See Type Material.
Diagnosis.-Densely, evenly clothed with scales of one size and one
color, green, blue, or white (4%); scales iridescent (as defined in
Methods) or not, never scintillating. Scales not imbricate on dorsal
surface of elytra. Usually (96%) with some scales on epistoma.
Natural bare areas, when present, the size of one scale, convex.
Flagellum 4.0-4.4 mm long. Spermathecal duct 4.3-4.5 mm long.
Description.-Male, length 7.0-8./7 mm, width 2.6-3.4 mm. Female,
length 7.5-9.0 mm, width 3.1-3.8 mm. Color as in Diagnosis, usually
with a strong sheen; scales of elytral intervals 7 and 8 often less
iridescent. Epistoma (Fig. 46) as in Diagnosis; averaging 1.2x longer
than wide; occupying 0.3 of anterior edge of rostrum. Rostrum (Fig.
41) flat (especially female) or feebly concave; median line finely
impressed from between eyes to interantennal line which may be weakly
elevated in maximum development. Prothorax averaging 1.2x wider than
long (range 1.1-1.29x); in dorsal view much wider than basal and
apical constrictions, sides rounded or parallel in male, in female
often widest posteriorly. Setae of prothorax erect in male, not erect
in female (one exception), as long as 1.5-3 scales. Postocular
vibrissae moderate. Elytra across humeri in male usually 1.1x, in
female 1.2x wider than prothorax. Elytra of male 2.5-2.8x, of female
2.9-3.3x longer than prothorax. Sides of elytra of male parallel or
Slightly wider behind middle, apex truncate, without a tooth. Sides
28 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
of elytra of female widest at about middle, apex slightly attenuated
beyond weak apical umbone or not, ending in a minute tooth or not.
Widest intervals of disc with up to 8 scales abreast. Setae of elytra
erect, as long as 2-5 scales in males, 2-4 scales in females. Female
usually with 4 (extreme 10) long, erect setae on sutural interval on
summit of declivity. Strial punctures not larger than a scale, may be
completely concealed by scales. Fore femur of male averaging 1.8x, of
female 1.6x wider than hind femur; with a weak, short distal flange.
Apical edge of fore tibia (Fig. 66) with narrow, rounded to acute lobe
next to inner edge; distal tooth of male approximately as long as
teeth on inner edge, shorter in female. Ventrite 5 of male moderately
to slightly convex, apex narrowly truncate, usually 2x wider than
long. Female sometimes with a few scales on perpendicular caudal
Surface of ventrites 2, 3, and 4; ventrite 5 across base averages 1.7x
wider than long, evenly squamose or scales somewhat sparser medially.
Male genitalia similar to Fig. 73 (see Remarks); aedeagus 2.2-2.7 mm
long, aedeagal apodeme 1.1-1.5 mm long, tegminal strut 1.3-1.5 mm
long, flagellum 4.0-4.4 mm long (1.7x longer than its aedeagus).
Spermatheca as in Fig. 116; spermathecal duct 4.3-4.5 mm long.
Type Material.-PARALECTOTYPES, HERE DESIGNATED, 10 males, 14
females: 1 male, 1 female, same data as lectotype but "Aug." (London);
1 male, 3 females, "Cuernavaca, Mor., Mex., Wickham" (London,
Washington); 2 males, 3 females, "Puebla, Mexico, Salle Coll."
(London); 2 males, 1 female, "Parada, Mexico, Salle Coll." (London,
Howden); 1 male, 1 female, "Istepec, Mexico, Salle Coll." (London,
Washington); 2 males, 2 females, "Boucard, Mex., Fry Coll." (London);
1 female, "1278, Mexico, Bowring 63.47" (London); 1 male, 2 females,
"Oajaca, 58.135 Mex." (London).
Distribution.-Map 1. MEXICO. Chiapas: Finca Guatimoc. Guerrero:
Amula, Chilapa, Taxco. Mexico: Ixtapan de la Sal. Morelos:
Cuernavaca, Tepoztl@n. Oaxaca: Istepec, Monte Alban, Parada. Puebla.
Specimens were collected in July, August, September, and October.
Specimens examined: 64 males, 47 females. Specimens in Auckland,
Basel, Berlin, Cambridge, Chicago, Dresden, Eberswalde, Leiden,
London, Los Angeles, Mexico, Paris, Stockholm, Washington, Howden,
O'Brien.
Remarks.-In the white specimen of fulgens figured in Tab. 7, Fig.
33, by Champion (1911), the prothorax jis actually 1.14x wider than
long, the figure being somewhat misleading. Champion mentions a
"claw" on the intermediate tibia of the male; this is the small] mucro
which is present on the hind and middle tibia of all Hadromeropsis
males.
There are three syntypes from Amula including the male lectotype
(not dissected) and a similar female. The third specimen is a male
which differs considerably from the above description of typical
fulgens. The discrepancies are as follows: postocular vibrissae more
numerous and longer; elytra 3.3x longer than prothorax, 1.3x wider
across humeri than across prothorax; elytral setae sparser and a few
setae on alternate intervals extremely long (as long as 8 scales);
distal tooth of fore tibia long; apex of ventrite 5 emarginate;
flagellum in curved position within aedeagus 6 mm long, 1.9x longer
than aedeagus (Fig. 73).
Most specimens of fulgens can be readily recognized
Howden: Hadromeropsis 29
macroscopically by the uniform color with a sheen. In addition to the
diagnostic characters, white specimens or worn specimens can be
separated on external characters from flagellatus by the lack of
punctures on the rostrum and head an y the weaker postocular
vibrissae; from dejeanii by the shape of the epistoma and smaller
scales; from opalinus by the very evenly distributed scales of
intervals 2 and 3 especially; from crinitus by the distal flange on
the fore femur and convex eye.
3. Hadromeropsis (Hadromeropsis) crinitus n. sp.
Figs. 40, 42, 43, 47, 77, 117, 131; Map 1
Diagnosis.-Densely, uniformly squamose as fulgens, but all dorsal
setae both sexes erect, longer, and denser than in fulgens. Eye large
and only feebly convex (Figs. 40, 42). Postocular vibrissae poorly
’ developed, no longer than adjacent setae. Fore femur without distal
flange. Aedeagus (Fig. 77) arcuate proximally only; remainder
straight, flattened dorsally and with dorso-lateral edges carinate.
Spermatheca as in Fig. 11/7, duct 1.3 mm long.
Description.-Holotype, male, length 9.1 mm, width 2.9 mm. Densely
clothed with scales of pinkish tan, obsoletely iridescent, without a
sheen; scales discrete, imbricate only on pronotum either side of
median line. Scales of ventral surface faintly opalescent whitish.
Naturally glabrous areas of elytra the size of a scale or less, except
sutural interval where scales are sparser. Setae of head and rostrum
as long as 3-4 scales; setae of prothorax as long as 5-/ scales, setae
of elytra as long as 5-8 scales. Rostrum approximately as wide as
long, dorso-lateral edges parallel, sides broadly visible in dorsal
view; flattened dorsally, apex rather strongly deflected, epistoma
thus almost vertical. Median line finely impressed between eyes only;
dorsal surface of rostrum with scattered fine punctures. Epistoma
(Fig. 43) occupying 0.4 of anterior edge of rostrum, 1.3x wider than
long, without scales. Head thick in profile (Fig. 40); eye large,
elongate, scarcely exceeding head in outline (Fig. 42). Prothorax
1.08x wider than long, sides slightly rounded between constrictions;
in profile, disc feebly arcuate, constrictions obsolete. Prothorax
with a very few small punctures, no pustules. Postocular vibrissae as
in Diagnosis, Fig. 40. Scutellum with a few scales and a few
appressed setae. Elytra across humeri 1.3x wider than prothorax.
Elytra 3.0x longer than prothorax. Humeri prominent, sides of elytra
very slightly convergent from humeri to apical 0.3, thence more
strongly convergent to apex, apical umbone weak in dorsal outline;
apices briefly individually rounded, without a tooth. Base of elytra
including scutellum abruptly perpendicular. Strial punctures small
and striae poorly defined, especially apically. Widest intervals 5
scales abreast; interval 5 narrower, as narrow as 3 scales abreast.
Setae very numerous on elytra (Fig. 47); uniform in length except
occasional setae of alternate intervals slightly longer. Fore femur
1.9x wider than hind femur, strongly but gradually swollen. Apical
edge of fore tibia with inner lobe approximately equal to distal
tooth, distal tooth 0.2 of width of apical edge. Last tergite in
30 Contrib. Amer. Ent..dnst., Vol. 19, no. 6, 1982
apical view scarcely convex. Abdomen long, convex; ventrite 5 (Fig.
131) convex, apex truncate, 1.7x wider than long. Genitalia as in
Diagnosis, Fig. //; aedeagus 3.3 mm long, aedeagal apodeme 1.3 mm
long, tegminal strut 1.8 mm long. Endophallic structure not seen,
internal sac damaged.
Allotype, female, length 9.0 mm, width 3.4 mm long. Differs from
type as follows. Rostrum with median line foveate between eyes.
Prothorax 1.2x wider than long; sides of prothorax with a few glabrous
pustules. Elytra across humeri 1.3x wider than prothorax. Elytra
3.6x longer than prothorax. Sides of elytra very slightly divergent
to apical 0.3, thence gradually, slightly rounded to apex, apical
umbone weaker than in male; sutural interval ending in a blunt tooth
about as long as a scale. Intervals and striae slightly more evident,
partly because intervals are feebly convex, especially basally and
laterally. Widest intervals up to 8 scales abreast. Setae of summit
of declivity on sutural interval little different from other setae of
same interval, but 9 setae slightly longer. Fore femur 1.5x wider
than hind femur. Ventrite 3 with caudal margin arcuate, posteriorly
directed. Ventrite 5 across base 1./x wider’ than _ long,
elongate-triangular, apex very narrowly rounded, slightly convex
longitudinally; scales on sides basally only. Spermatheca as in Fig.
117; spermathecal duct 1.3 mm long.
Type Series.-Holotype, MEXICO, [Michoacan], Patzcuaro, Koebele,
Koebele Collection (San Francisco). Allotype, same data as type (San
Francisco). No paratypes.
Remarks.-The wide epistoma is equalled or exceeded in flagellatus
and some opalinus. The elytral setae are more dense than on any other
species seen. The eyes may be as feebly convex in female flagellatus
and, less frequently, in female opalinus.
The internal sac was damaged in dissection and its form is
consequently unknown, but no obvious flagellum or sclerites were
observed. The tegmen is narrower in crinitus than in the other three
species in the group. The aedeagal apodemes are short as in aureus,
brevicomus, superbus. The length of the spermathecal duct 7s
"normal", i.e., not modified for a flagellum. These characters al]
indicate an internal sac with a short flagellate structure similar in
size to that of aureus, brevicomus, superbus.
H. crinitus occurs in an area from which I saw no other specimens
of Hadromeropsis. It is closest in characters and range to opalinus
to the Fei and fulgens from Guerrero. The diagnostic characters
listed will separate it from both.
The Latin word crinitus means hairy or with long hair.
4. Hadromeropsis (Hadromeropsis) flagellatus n. sp.
Figs. 45, 48, 68, 78-81, 113-115, 132, 133; Map 2
Diagnosis.-Often appearing dusty or slightly tessellate because of
arrangement of scales and long, erect setae. Clothed with white,
white and blue, iridescent green (especially in Veracruz), or coppery
scales. Scales often of several sizes, elytra often vaguely vittate
because of denser scales on intervals 2, 4, 6, and 8; vittae often
Howden: Hadromeropsis | 31
interrupted with irregular glabrous areas; with a vague V-shaped mark
before declivity in 14% of specimens; never evenly squamose as in
fulgens. Setae of head, prothorax and elytra long, fine, erect in
both sexes. Fore femur with weak to moderate distal flange (Fig. 48),
flange with at least a few shiny granules or tubercles in males and in
some females. Last tergite of male convex (especially northern part
of range), or flattened medially (especially center of range) or with
a longitudinal concavity (southern end of range). Genitalia extreme
(Figs. 78-81). Aedeagus 2.5-3.2 mm long, aedeagal apodeme 1.1-1.4 mm
long, tegminal strut 2.8-3.3 mm long, thus aedeagal apodeme less than
half the length of aedeagus, tegminal strut averaging as long as
aedeagus; ring of tegmen very wide; flagellum 9-11 mm long (3-4x
longer than aedeagus), longer than entire beetle. Spermathecal duct
7,.5-12.0 mm long.
Description.-Holotype, male, length 7.8 mm, width 2.8 mm. Shiny
black, sparsely clothed with white scales interspersed with gray-blue
scales, scales varying greatly in size and shape. Scales especially
Sparse on pronotum, scales of elytra forming a few vague clusters on
intervals 2 and 4. Dorsal setae fine, with long filamentous tips
mostly abraded in type; setae of male topotypes as long as 3 large
scales on head and rostrum, as long as 3-6 large scales on prothorax
as long as 4-7 large scales on elytra. Head and rostrum (Fig. 45 }
punctate, each seta arising from a puncture approximately as large as
a scale. Punctures of rostrum confluent apically, each puncture
bearing a scale or seta. Rostrum 1.2x longer than wide, dorso-lateral
edges distinct, parallel; sides of rostrum narrowly visible in dorsal
view. Median line marked with elongate pit between anterior half of
eyes; basal half of rostrum weakly concave. Epistoma approximately as
wide as long, occupying 0.4 of anterior edge of rostrum; epistoma
without scales, sides weakly carinate anteriorly. Segments 1 and 2 of
funicle equal; club approximately 3x longer than wide. Prothorax
1.13x wider than long, slightly convex, sides slightly rounded between
constrictions; constrictions obsolete on disc. Disc of prothorax with
a few fine punctures, sides of prothorax with base of some setae
weakly granulate. Postocular vibrissae consisting of about 8
moderately long, fine, white setae. Scutellum with a few small
scales, mostly glabrous. Elytra across humeri 1.3x wider’ than
prothorax. Elytra 3.1x longer than prothorax. Humeri prominent,
right-angled. Sides of elytra parallel to approximately apical 0.3,
apical umbone weak, apex beyond umbone broadly rounded, without a
tooth. Strial punctures uniform in size, moderate. Widest intervals
4 scales abreast, but scales not contiguous. Setae of ventral surface
and legs much more numerous than on dorsal surface, otherwise similar.
Fore femur (Fig. 48) 1.7x wider than hind femur; distal flange brief
but distinct, with shiny, sharp tubercles. Fore tibia (Fig. 68)
cyclindrica!; apical edge with inner lobe obsolete; distal tooth very
small, only 0.2 of width of apical edge. Ventrite 5 (Fig. 132)
Slightly convex, 2.2x wider than long, apex broadly emarginate. Last
tergite convex with a central flattened area; surface punctate.
Genttalia:’ as. ino P4¢,.- 78-81. Aedeagus flattened dorsally,
dorso-lateral edge sharp, almost carinate basally. Aedeagus 2.7 mm
long, aedeagal apodeme 1.1 mm long, tegminal strut 2.8 mm long,
flagellum more than 9 mm long.
32 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Allotype, female, length 8.7 mm, width 3.3 mm. Differs from type
as follows. Scales similar in color, but more dense; prothorax with
wide almost glabrous median and dorso-lateral vittae. Setae of head
and rostrum more numerous, most directed toward median line, as long
as 2-3 adjacent scales. Head more robust, eyes much less prominent.
Segment 2 of funicle 0.8x as long as segment 1; club 2.3x longer than
wide. Prothorax 1.16x wider than long, flat in profile; disc
indistinctly flattened laterally. Elytra across humeri 1.4x wider
than prothorax. Elytra 3.1x longer than prothorax. Elytra slightly
wider across middle; widest intervals 5 scales abreast; setae of
various lengths, as long as 3-8 scales, all setae of declivity longer;
Sutural interval at summit of declivity with 8 very long, erect setae.
Fore femur 1.4x wider than hind femur. Caudal margin of ventrites 2
and 3 anteriorly arcuate and caudal surface slanted anteriorly; caudal
margin of ventrite 4 straight, surface perpendicular. Ventrite 5
(Fig. 133) across base 1.8x wider than long, elongate-triangular, apex
narrowly rounded, slightly convex longitudinally; scales on sides
basally only, medially with only sparse, short setae. Allotype not
dissected; female topotypes with spermatheca as in Fig. 113,
spermathecal duct 8-8.5 mm long; duct scarcely wider or more
sclerotized at bursa.
Type Series.-Holotype, MEXICO, Tlaxcala, 21 mi W Apizaco, Aug. 20,
1958, E. Mockford, on juniper (Howden). Allotype, same data as type
(Howden). Paratypes, 43 males, 49 females. MEXICO. 1 female, Hoege,
Coll. Kuschel (Auckland); 2 males, 1888 [1], Coll. Kuschel (Auckland);
1 male, 1 female (Basel); 1 male, 2 females, F.C. Bowditch Coll.
(Cambridge); 6 males, 6 females, Koltze Coll. or Boucard [1], Jd.
Faust, Ankauf 1900 (Dresden*); 1 female, Hoege, Samm]. K.F. Hartmann
(Dresden); 1 male, 1 female, Coll. Kraatz, Hadromerus Opalinus Horn,
Hust. det. 1938 [1], Kuschel det. [1] (Eberswalde); 2 males, 1 female,
Sharp Coll. 1905-313 (London*); 1 female, Boucard, Fry Coll. 1905-100
(London); 1 female, Tylden Coll. (Oxford); 1 female, coll. de
Bonneuil, Ex. Coll. Clerc (Paris); 2 females, Hustache Coll. (Paris);
1 male, 1 female, ex Coll. Oberthur (Paris); 3 males, 1 female, Salle
1859 (Paris). Guerrero: 1 male, 1 female, Texquitzin bei Chilapa,
X.29, L. Schultze S.G. (Berlin). Hidalgo: 3 males, 1 female, 15 mi NE
Huichapan, 6900 ft, 8-18-1971, C & L O'Brien & Marshall (O'Brien); 1
male, 6 mi E Tulancingo, V1.24.1962, J.M. Campbell (Howden). Jalisco:
1 female (Mexico); 1 male, 5 mi NW Lagos de Ja Moreno, VII-16-1974,
R.L.Mangan & D.S.Chandler (O'Brien). Mexico: 1 female, D.F., J. R.
Inda Collector (Washington); 1 male, Ixtapan la Sal, 5500 ft,
9,VIII.1954, J. G. Chilcott (Ottawa); 2 males, 1 female, 5 mi SE
Texcoco, 30.VII.6/, on Mimosopsis aculeaticarpa Br. & Rs.(Howden); 1
female, 10 km de Villa Morelos, VIIT.26.1956, G. Halffter (Howden).
Puebla: 1 male, 3 females, Salle Coll. (London*, Howden*); 1 female
(Stockholm). San Luis Potos{: 1 male, Hacienda de Bleados, Dr. Palmer
(London*). Tlaxcala: 3 males, 5 females, same data as type, or H.F.
Howden [2] (Ottawa, Howden). Veracruz: 1 female, Deyr. (Cambridge); 1
male, 3 females, Jalapa, Hoege (London*, Washington*); 1 female, 2.3
mi W Acultzingo, /000 ft, Aug.24, 1951, J.E.Mosimann, T.M. Uzzell,
G.B. Rabb (Howden); 4 males, 3 females, El Camaron, Salle Coll.
(Dresden*, London*); 1 female, Cordova, Hoege (London*); 1 female,
Playa Vicente, Hoege (London*); 1 male, Las Vigas, Hoege, Sp. figured
Howden: Hadromeropsis 33
Ethe _maleocftiqueed. i iTabe te: . fits: 29. 1B. CeAesn: GO) wim by ted
(London*). No data: 5 males, 5 females (Cambridge, Dresden, London*,
San Francisco, Stockholm, Washington*).
* Bearing Champion label "B.C.A., Col., IV, pt. 3 Hadromerus
Opalinus Horn."
Remarks.-Paratypes vary as follows. Males vary in length from
7.4-9.0 mm and in width from 2.5-3.1 mm. Females vary in length from
8.1-10.4 mm and in width from 3.2-4.0 mm. Champion's illustration of
“opalinus" (1911, Tab. 7, Fig. 29) accurately depicts the form and
usty appearance of many specimens of flagellatus. The vittate
appearance of some specimens may be emphasized by the fact that
intervals 3 and 5 are often very slightly more elevated and scales
there are more frequently abraded from them leaving scales more
numerous in shallower intervals 2 and 4. #£Macroscopically most
Specimens appear white or whitish, 11% are green and only 3% are
distinctly coppery. No specimens were seen with scintillating scales
as in dejeanii, amoenus, etc.
The filamentous tips of dorsal setae are readily damaged; when
apparently entire, they may be of several lengths on the elytral
intervals and, infrequently, as much as twice as long on alternate
intervals. Setae of elytra are in single but irregular rows on each
interval on disc, more numerous on sutural and lateral intervals.
Females may have as many as 14 long setae on the sutural interval on
the declivity. The epistoma has 1 or more scales in 7% of the males,
18% of the females. The antennal club is variable in length. Widest
elytral intervals of females are up to 7 scales abreast. Apex of
elytra in females often with sutural interval produced in oblique
overlapping knobs or teeth, these teeth directed posteriorly in only
10% of the females. Fore femur of females often lack tubercles on the
inner distal edge. Inner lobe of the apical edge of the fore tibia
may be moderately developed; inner edge of fore tibia with as many as
16 teeth. Variation in genitalia is listed in the Diagnosis; the
Spermatheca varies in shape as in Figs. 114, 115.
The flagellum is always longer than the entire length of the
beetle and its proximal end is always very stiff. Within the beetle
the proximal end is found in one or two large loops or a figure "8"
over the proventriculus in the metathorax (Fig. 80). In one instance
the proximal end seemed to extend into the prothorax. A _ special
technique for dissecting these extreme genitalia is outlined in
Methods and Terminology.
No special technique was needed to dissect females; the extremely
long spermathecal duct was often found neatly and compactly folded
back and forth beside the spermatheca.
There is some indication of characters grading from the southern,
lower elevation part of the range to the central and northern part of
the range and higher elevations. "Southern" specimens are from E1
Camar6n (7), Cordoba (1), Playa Vicente (1), and "Mexico" (10 males, 4
females). They are characterized as follows: 55% clothed with
iridescent green scales (compared to only 7% from elsewhere); last
tergite of male with distinct longitudinal concavity (flattened or
convex elsewhere); flagellum 10, 10.5 and 11 mm in the three dissected
(9-10 mm in the four flagella measured of 10 others dissected);
spermathecal duct 8.7 and 10 mm in the two dissected (8-12 mm, average
34 CONTrID. Amers Ent; “Inst:; Vol. 19, no. 6; 1982
9.3 mm in the 10 others dissected). Males from the "center" of the
range have the last tergite flattened medially; this includes the type
locality of Apizaco in Tlaxcala, Chilapa in Guerrero, Puebla, Texcoco
(1 of 2 males) and Ixtapan la Sal in Mexico, and Las Vigas in
Veracruz. Males from the states of Hidalgo, San Luis Potos{, and some
from Mexico have the last tergite evenly convex.
H. flagellatus is most closely related to opalinus which differs
from flagellatus in the greatly reduced femoral flange, and
consequently the absence of tubercles or granules on the area of the
femoral flange, in the further reduction of the postocular vibrissae,
in the thickened apical edge of the elytra, in the prothoracic setae
not erect in either sex, and in the different genitalia. Apparently
opalinus is restricted to the Sierra Madre Occidental, extending as
far south as the Tropic of Cancer, whereas flagellatus occurs in the
Sierra Madre Oriental south of 22° as in Map 2.
Many specimens of fulgens have labels identical to those of
flagellatus. H. fulgens is most readily distinguished externally by
its more strongly rounded sides of prothorax, lack of punctures on
head and rostrum, denser scales, fine strial punctures, and longer,
slightly curved fore tibia.
The name flagellatus refers to the extremely long flagellum of the
males of this species.
The scintillans Group
5. dejeanii (Boheman) 10. aureus (Blanchard)
6. amoenus n. sp. 11. cretatus (Champion)
7. scintillans (Champion) 12. rufipes (Champion)
8. micans (Champion) 13. superbus (Heller)
9. brevicomus n. sp.
Characteristics of Group.-Scales scintillating, iridescent or
neither, without a sharply defined color pattern, often with a pattern
formed by size and arrangement of small glabrous areas. Without
tubercles or pustules on prothorax or elytra but aureus, and to a
lesser extent brevicomus, with a tendency for glabrous areas to be
slightly elevated. Setae of elytra in some species much longer on
alternate intervals. Fore tibia at least slightly curved and at least
slightly bowed distally (except some scintillans). Endophallic
structure a flagellum, but not known for micans and rufipes. Female
without bursal sclerites; spermathecal duct proportionate in length to
that of flagellum.
Remarks.-Of the other two flagellate species groups, the opalinus
group differs from the scintillans group in the straight fore tibia
and wide tegmen and the gemmifer group differs in the presence of a
tubercle on the fore coxa on the inner distal edge.
5. Hadromeropsis (Hadromeropsis) dejeanii (Boheman)
Pigs. 44.71, 82, 83,, 118s.Map: 1
Hadromerus dejeanii Boheman, 1840:293. Champion, 1911:183; Tab. 7,
Howden: Hadromeropsis 35
Fig. 27. Type, male, labelled "34" mechanically printed on white
square, "Vera Crux in Mexico, Chevr. 675" hand written on pale
blue coated paper, "9" printed on white paper, "Typus" on red
paper rectangle outlined in black, '"dejeani [sic] Chevr."
penciled on yellow paper, "163, 53" on salmon paper (Stockholm).
Diagnosis.-A short, stout species uniformly clothed with large,
flat, scintillating green scales, or with smaller iridescent scales
interspersed, or (1 female) with iridescent scales only. Epistoma
long and narrow (Fig. 44), often connected to median line by glabrous
line; occupying only 0.1-0.3 of anterior edge of rostrum. Setae of
pronotum in both sexes appressed, as long as 1-1.5 scales. Fore femur
stout, with strong distal flange on inner edge. Fore tibia (Fig. 71)
often evenly arcuate, or bowed apically only. Apical edge of fore
tibia of male with weak to obsolete lobe near inner side; in female
lobe obsolete to absent. Aedeagal apodeme very long, 0./6 as long as
aedeagus; flagellum 4.9-5.5 mm long.
Description.-Male, length 6.8-8.5 mm, width 2.6-3.1 mm. Female,
length 8.0-9.6 mm, width 3.1-4.2 mm. Scales imbricate or discrete.
Glabrous areas of pronotum rather evenly distributed, approximately
the size of a scale, occasionally confluent, weakly convex; often with
median line partly glabrous. Glabrous areas of elytra ranging in size
from less than the diameter of a scale to the size of several scales;
areas flat to weakly convex. Rostrum (Fig. 44) flat to concave,
median line often narrowly glabrous and connected to apex of epistoma,
thus emphasizing the length of the epistoma. Epistoma usually
approximately 2x (range 1.3-2.0x) longer than wide; epistoma occupying
0.19-0.26 in male, 0.23-0.38 in female of anterior edge of rostrum;
epistoma with 1 or more scales in 17% of males, 15% of females.
Antennal club short, length 0.6-0.8 mm in male, 0.6-0.7 mm in female.
Prothorax convex, sides strongly rounded, averaging 1.1x wider than
long. Setae of pronotum as in Diagnosis. Postocular vibrissae
moderate. Elytra across humeri 1.2x wider than prothorax. Elytra of
male 2.5-2.7x, of female 2.8-3.2x longer than prothorax. Sides of
elytra of male parallel, elytra of female wider apicad of middle. In
both sexes apical umbone weak, distinct; apex truncate, without a
tooth. Widest intervals of disc with 5 or 6 scales abreast. Setae of
elytra in both sexes stiff, erect, as long as 2-3 scales, those of
alternate intervals may be slightly longer than those of other
intervals. Female with an average of 6 (extreme 12) long, erect setae
On sutural interval at summit of declivity. Fore femur as in
Diagnosis; in male 1.8-2.2x, in female 1.4-1./x wider than hind femur.
Fore tibia as in Diagnosis and Fig. 7/71, with some small, shiny
pustules on posterior surface near teeth. Ventrite 5 of male 2.0-2.2x
wider than long, moderately convex, apex broadly truncate-emarginate.
Last tergite of male convex. Ventrite 5 of female 1.8-2.0x wider than
long, sparsely squamose, almost flat. Male genitalia as in Figs. 82,
83; aedeagus 2.8-3.2 mm long, aedeagal apodeme 2.3-2.6 mm long,
tegminal strut 2.0-2.2 mm long, flagellum within aedeagus 4.9-5.5 mm
long. Spermatheca as in Fig. 118; spermathecal duct 5.9-6.0 mm long.
Distribution.-Map 1. MEXICO. Chiapas [see Remarks]. Nuevo Leon:
Santiago. San Luis Potosf: 6 mi E Ciudad del Maiz, 4400 ft. Veracruz:
Cérdoba, El Camar6n, Jalapa, Orizaba, Playa Vicente.
Specimens were collected in July and August. A series of specimens
36 Contrib. Amers vents -Inst.; VOT 19, no. 6, 1982
from Santiago, Nuevo Leon, was taken on pear trees.
Specimens examined: 31 males, 18 females. Specimens in Auckland,
Berlin, Dresden, Eberswalde, Leiden, London, Paris, San Francisco,
Washington, Howden, O'Brien.
Remarks.-Champion's description and illustration of dejeanii are
accurate. H. dejeanii superficially resembles brevicomus in the
Characters of the prothoracic setae, body shape, etc., but differs in
the more evenly distributed glabrous areas of the elytra (concentrated
medially in brevicomus), scintillating scales (iridescent in
brevicomus), and very different male and female genitalia. The
aedeagal apodomes are longer in dejeanii than in any other species in
the nominate subgenus.
Only a pair of specimens of dejeanii labelled "Chiapas, ex. Col.
Salle" (Dresden) indicate that dejeanii possibly overlaps the range of
scintillans and brevicomus. H. scintillans, although often similarly
clothed with green scintillating scales, is not as closely related and
can be readily distinguished by its elongate body, long dorsal setae,
euc.
6. Hadromeropsis (Hadromeropsis) amoenus n. sp.
Figs. 84-86, 121, 134, 135; Map 3
Diagnosis.-Strongly resembling a Guatemalan scintillans but
flagellum and spermathecal duct measuring approximately only one-third
as long and occurring north of the Isthmus of Tehuantepec. Sympatric
with dejeanii and similar to it in color but fore tibia usually less
bowed, elytra longer, female with tooth on apex of sutural interval,
genitalia different. Flagellum shorter than aedeagus, 1.3-2.0 mm
long; proximal end with a heavy collar (Figs. 85, 86). Spermathecal
duct 1.5-2.2 mm long.
Description.-Holotype, male, length 8.5 mm, width 2.7 mm. Elytra
and sides and dorsum of prothorax clothed with large, green
scintillating scales; remainder of body and legs clothed with pale,
iridescent pinkish scales with occasional scintillating green scales.
Scales contiguous or not, nowhere forming a vitta; glabrous areas
smooth, polished black, irregular in shape on pronotum, glabrous areas
of elytra of various sizes, sometimes as wide as intervals and
continuous with adjacent glabrous areas, thus forming vague, short,
wavy fasciae; glabrous areas smaller towards apex, on declivity the
size of one or more scales. Rostrum approximately as wide as long,
dorsal surface very slightly inclined towards median line; median line
glabrous, very finely impressed between eyes only. Epistoma occupying
0.3 of anterior edge of rostrum, without scales, 1.4x longer than
wide. Segment 2 of funicle 1.3x longer than segment 1; club 3.6x
longer than wide, 0.8 mm long. Prothorax 1.08x wider than long,
strongly convex, sides strongly rounded between constrictions, basal
constriction complete, apical constriction obsolete on_ disc;
postocular vibrissae well developed. Setae of disc of pronotum as
long as 1.5-2 scales, setae of sides of prothorax as long as 2-3
scales, setae matted except a few basal setae erect. Scutellum
covered with scales and a few fine, appressed setae. Elytra across
Howden: Hadromeropsis 3/7
humeri 1.2x wider than prothorax. Elytra 2./5x longer than prothorax.
Elytra shaped as in scintillans. Strial punctures subfoveate basally,
becoming smaller towards apex. Widest interval 4 scales abreast.
Setae of elytra obviously worn on type; erect; in male paratypes some
setae of alternate intervals longer, shorter setae as long as 2.5
scales, longest setae as long as up to 6 scales. Fore femur 1.9x
wider than hind femur, distal flange well developed, its edge with a
few acute pustules lower than the diameter of one scale. Fore tibia
as in scintillans, distal tooth as long as 0.5 of width of apical
edge. Ventrite 5 (Fig. 134) slightly convex, 2x wider than long, apex
broadly truncate, shallowly emarginate. Last tergite convex.
Aedeagus as in Fig. 84; apex cupped, not depressed ventrally; dorsally
testaceous and flexible from orifice to apical 0.28 of total length of
aedeagus. Aedeagus 2.4 mm long, aedeagal apodeme 1.2 mm _ long,
tegminal strut 1.4 mm long, flagellum 1.4 mm long.
Allotype, female, length 10.1 mm, width 4.0 mm. Differs from type
as follows. All scales scintillating green. Glabrous areas smaller,
seldom the width of one elytral interval. Epistoma occupying 0.26 of
anterior edge of rostrum, 2.1x longer than wide. Segment 2 of funicle
1.1x longer than segment 1; club 3.3x longer than wide, 0.7 mm long.
Prothorax 1.1x wider than long, much less convex. Elytra across humeri
1.3x wider than prothorax. Elytra 3.3x longer than prothorax.
Alternate intervals of elytra with a few very long setae basally and
apically; most setae as long as 2 scales, the very long setae as long
as 4 scales. Widest intervals 6 scales abreast. Sutural interval at
summit of declivity with 6 or more long, erect setae. Apex of sutural
interval with short, distinct tooth. Fore femur 1.3x wider than hind
femur. Ventrite 5 (Fig. 135) as in scintillans female. Spermatheca
as in Fig. 121; spermathecal duct broken in allotype, 1.5-2.2 mm in
paratypes. .
Type Series.-Holotype, MEXICO, Veracruz, Jalapa, 9/28-X/3/61, R &
K Dreisbach (Howden). Allotype, same data as type (Howden).
Paratypes, 13 males, 16 females. MEXICO. [Oaxaca?] : 1 male, Juquila,
Flonr S. (Berlin). Puebla: 1 female, Crawford Lsyntype of Hadromerus
micans Champion] (London); 1 male, 1 female, 6 mi. W Teziutlan, Aug.
18, 1958, R.B. Selander (Howden). Veracruz: 6 males, 6 females, same
data as type, or VIII/1-6/61 Ll female] (Paris, Washington, Howden,
O'Brien); 2 females, no additional data (San Francisco); 1 female, 10
km N Fortin, July 21-29, 1976, E. Giesbert Coll (Los Angeles); 1 male,
Las Vigas, Hoege Lopalinus Horn, det. Ch.] (London); 1 male, 1 female,
13 mi E Las Vigas, VI-29-1962, J.M. Campbell (Ottawa, Howden); 1 male,
Orizaba, HHS & FDG, Dec. 1887 Lsyntype of Hadromerus scintillans
Champion] (London); 1 female, Orizaba, Flohr S. (Berlin); I male,
Orizaba, 25.VII.1978, G & M Wood (Howden); 1 female, Playa Vicente,
Hoege Lopalinus Horn, det. Champion] (London); 1 male, Playa Vicente,
Hoege Lsyntype of Hadromerus scintillans Champion] (London). No data:
1 female, S. Mex. Lopalinus Horn, det. Champion] (London); 1 female,
Mex., F.C. Bowditch Coll. (Cambridge).
Remarks.-Males vary in length from 7.7-9.1 mm and in width from
2.8-3.1 mm. Females vary in length from 8.1-11.4 mm and in width from
3.1-4.1 mm. All but four specimens were completely clothed with
scintillating green scales. One male from Las Vigas was entirely
Clothed with slightly convex iridescent pinkish scales but with
38 Contrib. Amerc Ent. “Inst., vol.°19, no. 6, 1982
occasional flat scintillating scales, the iridescent scales of the
middie and hind femora more green than pink. In the other Las Vigas
male there are iridescent scales intermingled everywhere with the
scintillating green. In one female from Playa Vicente the scales are
about one-half scintillating green and most of the remainder are
slightly convex non-iridescent whitish. In the female from "S. Mex."
iridescent green scales outnumber the occasional opalescent scales.
In amoenus as in scintillans, a distal portion of the epistomal edges
are shiny and weakly carinate. Scales encroached on the epistoma in
two males and four females. The antennal club of the male ranges from
3-4x longer than wide. Glabrous spots on the prothorax were slightly
elevated in one male from Las Vigas and one male from Orizaba. Setae
seem to be particularly delicate in this species, but even in the
freshest specimens only occasional setae were erect on the pronotum.
In the largest females the widest intervals occasionally were 7 scales
abreast. The female elytral tooth ranges from scarcely perceptible to
as long as 4 scales. The fore tibia is definitely bowed in the male
from 13 mi E Las Vigas. Male genitalia varies as follows: aedeagus
2.1-2.5 mm long, aedeagal apodeme 1.0-1.3 mm long, tegminal strut
1.2-1.5 mm long, flagellum 1.3-2.0 mm long. Spermathecal duct is
1.5-2.2 mm long.
Vague, wavy, slightly elevated transverse glabrous lines were
present on the elytra in half the male paratypes and may be helpful in
tentative identification of males. I did not see such elytral
markings in any specimens of the sympatric dejeanii, but they are
distinct in brevicomus described here from Chiapas.
In addition to dejeanii, H. amoenus is also sympatric with
flagellatus and is readily separable from the latter by the convex
prothorax, narrower epistoma, bowed apex of fore tibia and characters
of the genitalia.
The locality is helpful, but examination of the male and female
genitalia is usually necessary for positive identification of amoenus
among other species of the scintillans group.
Particular care should be exercised regarding a locality of
"Jalapa" not associated with a state. Jalapa is the name of a
medicinal plant and towns of that name abound outside the known range
of amoenus.
This species is named amoenus, meaning "pleasant, delightful”,
partly in reference to the physical attractiveness of the specimens
and partly in memory of the late R.R. and Kay Dreisbach, a delightful
couple who thoroughly enjoyed collecting insects and sharing their
catch with others.
7. Hadromeropsis (Hadromeropsis) scintillans (Champion)
Figs. 69, 87-89, 120, 136, 137; Map 3
Hadromerus scintillans Champion, 1911:182; Tab. 7, Figs. 25, 26.
LECTOTYPE, HERE DESIGNATED, male, on card with female, labelled,
"Outche Mts 230 7=9000 Ft. << Chamption, ur" ey "B.C A. Coke WV,
pt.3, Hadromerus scintillans, Ch." (London). See Type Material.
Diagnosis.-Very variable, the range (Guatemala to Chiapas and
Howden: Hadromeropsis 39
Tabasco in Mexico) and the characters of the genitalia often necessary
for recognition. Setae (see caution in Methods) of entire body erect
in male; in female, setae may or may not be erect on head and
prothorax. Elytra with humeri prominent; setae of alternate intervals
distinctly longer. Fore femur with flange moderately to well
developed. Apical edge of fore tibia (Fig. 69) divided into two lobes
subequal in length and often in width. Flagellum within aedeagus
measures 4.1-6.0 mm long. Spermathecal duct measures 4.3-/7.0 mm long.
Description.-Male, length 7.5-9.1 mm (Guatemala specimens),
6.8-9.3 mm (other localities); width 2.7-3.2 mm (Guatemala specimens),
2.5-3.1 mm (other localities). Female, length 8.9-10.0 (Guatemala
specimens), 7.6-10.0 mm (other localities); width 3.2-3.8 mm
(Guatemala specimens), 2.0-3.8 mm (other localities). Typical
(Guatemala) specimens densely clothed with green scintillating scales,
scales randomly discrete or overlapping. Specimens from other
localities with scales as in Guatemala specimens or one of the four
following patterns. Pattern 1, scales of elytral intervals 3, 8, and
9 more dense, forming a tone-on-tone vitta. Pattern 2, hind legs and
often venter tan; scales slightly convex, whitish, tan or slightly
pinkish, not at all scintillating or iridescent (Montebello,
Teopisca), or with varying amounts of metallic reflections (Bochil,
Las Margaritas, San Crist6bal, Teopisca). Pattern 3, bicolored with
green and pinkish scales, e.g., dorsum green, venter pinkish or the
reverse, or head and prothorax pinkish, elytra green; or elytral
intervals 4 to 7 green and remainder pinkish (San Crist6bal). Pattern
4, venter and legs black, scales sparser exposing shiny black
integument; all scales macroscopically silvery, rosy or tan, under
magnification appearing brilliant, scintillating colors, especially
red, green, and gold, each scale one color but all colors on each
specimen; these specimens usually with vittae on elytral intervals 3,
8 and 9 and scales often very sparse between vittae (Montebello, San
Crist6ébal, San Felipe, Simojovel, Villahermosa). Densely squamose
specimens with random glabrous spots on prothorax and elytra; glabrous
spots largest on basal portion of elytra, becoming much smaller on
declivity; females more densely squamose than males of all patterns.
Rostrum slightly concave medially and median line usually narrowly
glabrous (Guatemala specimens); rostrum flattened (patterns 1, 2,
or slightly concave (pattern 4) and median line occasionally glabrous;
median line not impressed except between eyes. Epistoma occupying
0.25-0.3 of anterior edge of rostrum in male, 0.2-0.4 in female.
Epistoma with 1 or more scales in 83% of specimens from Guatemala, 13%
of other specimens. In Guatemala specimens, prothorax of male convex,
sides strongly rounded, averaging 1.08x wider than long; prothorax of
female slightly less convex dorsally, sides less rounded, averaging
1.14x wider than long. Prothorax of pattern 1, 2, and 3 specimens
averaging 1.1x wider than long in male, 1.14x in female. Prothorax
of pattern 4 specimens averaging 1.08x wider than long in male, 1.13x
in female. In profile prothorax of Guatemala specimens with basal
constriction distinct, apical constriction slightly less so; often
with vague dorso-lateral depression; other specimens similar or not;
glabrous area of disc flat to slightly pustulate. Median line often
partially faintly impressed or glabrous or both. Setae of disc of
prothorax erect in male; female with no setae on disc erect (Guatemala
40 Contrib. Amer. EAC TAS. vor.'19, fo. 6, 1982
specimens) or erect on basal third (most specimens of patterns 1, 2,
and 3), or all setae erect (specimens of pattern 4 and some others).
Postocular vibrissae moderate to well developed. Scutellum covered
with scales and a few appressed setae or (pattern 4) setae only.
Elytra across humeri average 1.3x (range 1.2-1.4x) wider than
prothorax in male, 1.4x (range 1.3-1.5x) in female. Elytra average
2.9x (range 2.7-3.1x) longer than prothorax in male, 3.4x (range
3.1-3.7x) in female. Humeri prominent; in male elytra widest across
base, sides parallel or gradually tapered, in female elytra widest
apicad of middle; apical umbone distinct in both sexes. Apex of
elytra slightly longer than in dejeanii, that of female usually with a
short tooth. Widest intervals of disc with 5 or 6 scales abreast
(extreme, 8). Setae of alternate elytral intervals much longer on
apical portion and occasionally longer on base. Female with an
average of 8 long, erect setae on sutural interval at summit of
declivity. In densely squamose specimens, strial punctures the size
of a scale or smaller; in more sparsely squamose specimens, strial
punctures may be foveate, especially near base of elytra. Fore femur
of male averages 1.8x wider than hind femur (Guatemala specimens) or
2x (pattern 4) or 2.2x (others). Fore femur of female averages 1.4x
wider than hind femur in Guatemala specimens, 1.5x in all others.
Fore femur with distal flange moderately to well developed, weaker in
female, its edge often with a few small acute pustules. Fore tibia
(Fig. 69) weakly arcuate distally or not, apical edge as in Diagnosis,
distal tooth acute, usually longer than teeth of inner edge. Ventrite
5 of male (Fig. 136 of Quiché specimen) moderately convex, averaging
2x wider than long, apex broadly, shallowly emarginate. Last tergite
of male convex. Ventrite 5 of female averaging 1./x wider than long
(Fig. 137 of Guatemala specimen) (Guatemala and patterns 1, 2, and 3), °
1.5x in pattern 4 specimens; ventrite very slightly convex, squamose
as remainder of abdomen. Male genitalia as in Figs. 87-89. In
Guatemala and pattern 1, 2, and 3 specimens, aedeagus 2.4-2.5 mm long,
aedeagal apodeme 1.6-1.9 mm long, tegminal strut 1.3-1./ mm long,
flagellum 4.1-4.8 mm long; in pattern 4 specimens, aedeagus 2.3-3.2 mm
long, aedeagal apodeme 1.7-2.0 mm long, tegminal strut 1./-2.0 mm
long, flagellum 4.7-6.0 mm long. Spermatheca as in Fig. 120. In
Guatemala and patterns 1, 2, and 3 specimens, spermathecal duct
4.0-5.5 mm long, in pattern 4 specimens, 5.5-/7.0 mm long.
Type Material.-None of the specimens in the type series bears the
usual “Sp. figured" label. There is a "Type" label on the pin of one
card bearing a male and female and labels like the lectotype, but this
"Type’ label is thought to have been affixed by Arrow or someone other
than Champion (R. Thompson, in litt.).
PARALECTOTYPES, HERE DESIGNATED, 7 males, 14 females. GUATEMALA.
2 males, 6 females, no additional data (London); 3 males, 5 females,
same data as type (London, Washington); 1 male, 2 females, Tepan
(London, Howden). MEXICO. 1 female (London). Locality in doubt, 1
male, Costa Rica, "locality doubtful" in Champion's handwriting
(London).
Two of Champion's syntypes are actually amoenus. These are 1 male
labelled "Orizaba, H.H.S. & F.D.G. Dec. 1887" (London), and 1 male,
labelled "Playa Vicente, Mexico, Hége" (London). One male syntype
with no data is dejeanii. )
Howden: Hadromeropsis Al
Distribution.-Map 3. GUATEMALA. Chimaltenango: Tecpan (="Tepan"),
Zaragoza. El Quiché: Quich@ Mts. Huehuetenango: 25 mi §
Huehuetenango. MEXICO. Chiapas: 8 mi N Bochil, Comitan, 12 mi NW
Comitén, 14 mi W Comitan, Dolores, Las Margaritas, 8 mi W PN
Montebello, 10 mi W P N Montebello, Rancho Nuevo (8.6 mi E San
Crist6bal), San Crist6bal de las Casas, 5 mi SE San Cristobal, 35 mi E
San Crist6bal, San Felipe, 2 mi S Simojovel, Teopisca, 2 mi SE
Teopisca, 8 mi SE Teopisca, 9 mi SE Teopisca, 28 mi E Tuxtla
Gutiérrez. Tabasco: Villahermosa.
In addition to the "Costa Rica" paralectotype, a locality which
Champion questioned, there are two specimens in Berlin labelled "Costa
Rica, Wagner" and one specimen in Stockholm labelled "Costa Rica, D.
Geminger'. I suspect these refer to something other than the country
now known as Costa Rica.
Specimens were collected in May (1), June, July, August (1),
September (4), and December (1).
Specimens examined: 81 males, 63 females. Specimens in: Berkeley,
Berlin, Cambridge, Dresden, Eberswalde, Leiden, London, New York,
Ottawa, Paris, Stockholm, Washington, Howden, O'Brien.
Remarks.-The figure in the color plate in Champion (1911: Tab. 7,
Fig. 25) shows the elytra too short.
The black legged specimens (pattern 4) are primarily from the
lower elevations and are often distinguishable on morphological
Characters. However, no characters appear to be exclusive to one area
and the mingling of characters is such that only field work could
justify a different treatment.
At 9 mi SE Teopisca H. Howden collected scintillans on Acacia, an
unidentified legume, and on oak. At 8 mi WP. N. Montebello, O*Brien
and associates collected five scintillans on Juniperus mexicana; at 12
mi S Comitaén they took a series of scintillans on Quercus.
8. Hadromeropsis (Hadromeropsis) micans Champion
Figs. 70, 119, 139; Map 3
Hadromerus micans Champion, 1911:183; Tab. 7, Figs. 28, 28a.
LECTOTYPE, HERE DESIGNATED, female, labelled, "Purula, Vera Paz,
Champion," "¢%," "Type" on orange-circled disc, "Sp. figured,"
"B.C.A., Col., IV. pt. 3, Hadromerus micans, Ch.," "Lectotype" on
purple-circled disc (London). See Type Material.
Diagnosis.-Known only from the female lectotype. Very large and
robust. Resembling Guatemalan scintillans but apex of ventrite 5
pointed, spermatheca (Fig. 119) with ramus not at all produced,
spermathecal duct 7.0 mm long.
Description.-Unique female, length 13.4 mm, width 5.4 mm. Habitus
as in Champion (1911, Tab.7, Fig. 28). All scales scintillating
green, dense but overlapping only around eye and on specific areas of
ventral surface such as coxae. Glabrous areas as in Champion
(1911:183 and Tab. 7, Fig. 28). Rostrum with dorso-lateral edges
slightly divergent apically where rostrum is approximately as wide as
long. Median line glabrous, impressed between eyes, thence obsoletely
elevated to apical 0.6 at a vague transverse elevation; epistoma
42 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
- reaching almost to this transverse mark. Epistoma occupying 0.3 of
anterior edge of rostrum; epistoma 1.4x longer than wide, its distal
emargination extending 0.3 of length of epistoma; 2 scales on
epistoma. Segment 2 of funicle 1.2-1.4x longer than segment 1, club
3.2x longer than wide. Prothorax 1.15x wider than long, sides only
moderately rounded, slightly flattened dorso-laterally; in profile
scarcely convex with basal and apical constrictions faint. Setae of
prothorax very fine, erect basally only, as long as 2-3 scales.
Postocular vibrissae well developed. Scutellum with a few scales and
a few setae. Elytra across humeri 1.5x wider than prothorax. Elytra
3.3xX longer than prothorax. Humeri very prominent, interval 5 at base
depressed thus further emphasizing humeri. Elytra with post-scutellar
area flattened. Tooth at apex of sutural interval approximately as
long as 3 scales. Widest interval with extreme of 9 scales abreast,
usually 5-/ scales abreast. Setae of alternate intervals longer
basally and apically, the longest as long as 9 scales, shorter setae
as long as 2 or more scales. Sutural interval on declivity with 9-12
very long erect setae. Strial punctures smaller than a scale. Fore
femur 1.36x wider than hind femur, distal flange weak. Fore tibia as
in Fig. /0, distal tooth acute, 0.5 as long as width of apical edge.
Ventrite 5 (Fig. 139) convex as in scintillans, evenly covered with
scales as remainder of abdomen; 1.7x Tonger than wide, sides
convergent from base to apex in a blunt point. Spermatheca as in Fig.
119; spermathecal duct / mm long.
Type Material.-The syntype from Puebla is described as a paratype
of amoenus in this paper; its spermathecal duct is only 1.8 mm long.
| Distribution.-Map 3. GUATEMALA. Baja Verapaz: 1 female, PuruYa
London).
Remarks.-This is possibly only an extremely large and robust
specimen of scintillans, but the different spermatheca seems to be
sufficient justification to let it stand until field observations or
more material can elucidate the situation.
The large size and somewhat similar spermatheca bring to mind
cretatus, but in that species the base of the elytra is distinctly
arcuately emarginate instead of straight.
9. Hadromeropsis (Hadromeropsis) brevicomus n. sp.
Fags; 00x: Slivi22. 1233) Map: Zz
Diagnosis.-Densely clothed with white (1 female) or iridescent
green scales, dorsum usually with a slight coppery or golden lustre in
reflected light; glabrous areas of elytra often as wide as one
interval, these areas larger on intervals 1, 2, and 3 where they often
coalesce to form short, vague, sinuous fasciae. Setae of prothorax in
both sexes appressed, very short, as long as one scale on center of
disc, on sides maximum length of 2 scales. Endophallic structure
(Figs. 90, 91) less than half the length of the aedeagus, bent and
very stout proximally, with short flagellum. Spermathecal duct very
Short, 0.9-1.4 mm long.
Description.-Holotype, male, length 9.0 mm, width 3.2 mm. Scales
and glabrous areas as in Diagnosis. Scales especially dense and
Howden: Hadromeropsis 43
overlapping on side of rostrum and head, side of prothorax, side of
fore coxa, side of meso- and metasternum. Dorsum of head, rostrum and
prothorax with glabrous areas irregular in size and placement, as
large as 1 to many scales. Glabrous areas of elytra forming 5
irregular sinuous lines, the longest reaching stria 4, the glabrous
areas polished and slightly elevated. Rostrum 1.12x longer than wide;
dorso-lateral edges distinct, parallel, glabrous. Median line
glabrous entire length, impressed between eyes. Dorsal surface of —
rostrum with faint transverse interantennal elevation at about middle,
very slightly concave caudad of elevation; basal glabrous surface
punctate, slightly rugose. Epistoma occupying 0.2/7 of anterior edge
of rostrum, 1.3x longer than wide; without scales. Funicle with
segment 2 scarcely longer than segment 1; antennal club 3.8-4x longer
than wide. Prothorax 1.12x wider than long, convex; sides rounded,
much wider than constrictions. In profile pronotum strongly convex
basally, less so anteriorly, anterior constriction distinct though
weak. Setae of prothorax as in Diagnosis; on disc glabrous base of
setae with a faint crescent-shaped elevation, elevation’ less
pronounced on sides. Postocular vibrissae well developed. Elytra
across humeri 1.2x wider than prothorax. Elytra 2.6x longer than
prothorax. Base of elytra slightly arcuately emarginate between
Striae 5. Sides of elytra parallel to approximately apical third,
thence slightly rounded, apical umbone distinct in outline, apex
elongate-rounded, without a tooth. Elytra in profile thick as in
dejeanii, but declivity more gradual. Widest interval with 7 scales
abreast, most intervals 5-6 scales abreast. Strial punctures
moderate; those of sutural interval and interval 2 basally foveate,
gradually becoming smaller apicad. Elytral setae of two types; short
curved setae on disc as long as 1 scale, becoming longer, straighter
on declivity and on sides; alternate intervals, including interval 7,
with much longer, straight, erect setae in addition; sutural interval
with intermediate length, slightly arcuate setae. Fore femur 1.9x
wider than hind femur, strongly swollen, with moderate arcuate flange
on distal edge. Fore tibia weakly bowed, apical edge with distinct
small lobe near inner edge; distal tooth as long as 0.5 of apical
width of tibia; ventral surface with some indistinct sculpturing and
near inner edge with very small, shiny tubercles. Metasternum
protuberant compared to many species, this especially evident in the
broadly concave posterior median pit and the abrupt ledge adjacent to
the hind coxa. Ventrite 5 convex, 1.9x wider than long, apex
emarginate. Last tergite convex but with high point’ slightly
flattened. Genitalia as in Diagnosis and Figs. 90, 91. Aedeagus 2.4
mm long, aedeagal apodeme 1.1 mm long, tegminal strut 1.1 mm long,
endophallic structure 1.0 mm long.
Allotype, female, length 9.3 mm, width 3.7 mm. Differs from type
as follows. Scales sparser on mesepisternum and metepimeron (but this
not a sexual expression in_ paratypes). Rostrum more robust,
dorso-lateral edges weakly bowed outward. Epistoma 1.4x longer than
wide. Prothorax less convex, apical constriction not marked on disc;
1.09x wider than long. All prothoracic setae as long as 1 scale
except at extreme anterior and basal edges on sides. Elytra across
humeri 1.36x wider than prothorax. Elytra 3x longer than prothorax.
Sides of elytra slightly divergent to apical third thence gradually
44 _ Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
rounded, forming apical umbone, apex triangular with arcuate sides;
sutural interval with very weak distal tooth. Sutural interval at
summit of declivity with 5 longer setae of graduated lengths.
Ventrite 5 slightly convex apically, 1.8x wider than long, apex
narrowly rounded; medially with short setae, few scales. Spermatheca
(Fig. 122) 0.8 mm long, spermathecal duct 0.9 mm long.
Type Series.-Holotype, MEXICO, Chiapas, / mi SW Ocozocoautla,
2500", Aug 1 1974, O'Brien & Marshall, on Acacia pennatula (O'Brien).
Allotype, same data as type (O'Brien). Paratypes, 5 males, 2 females.
MEXICO. Chiapas: 3 males, 1 female, same data as type (Howden,
O'Brien); 2 males, El Sumidero, 14 Sept. 1974, G. Bohart, W. Hanson
(O'Brien); 1 female, 14 km N. Tuxtla Gutiérrez [Sumidero, approx.
4000'], VI1.14.1962, J. M. Campbell (Howden).
Remarks.-Males vary in length from 7.9-9.5 mm and in width from
2./-3.4 mm. The female paratypes are 9.0-9.5 mm in length and 3.8 mm
in width. The female from the type locality is clothed with white
scales only, otherwise paratypes exhibit little variation. The green
female paratype and one male from £1 Sumidero are more densely and
more evenly squamose, the elytral glabrous areas rarely as wide as an
interval. No specimens have scales on the epistoma. The antennal
club of males is 3.0-3.8x longer than wide, of females 3.1-4.0x longer
than wide. In dejeanii the antennal club of males is 2./7-4.0x longer
than wide, in females 2.2-3.0x longer than wide.
Five males and three females were dissected. Variation in the
male genitalia is as follows: aedeagus 2.3-2.4 mm long, aedeagal
apodeme 1,0-1.3 mm long, tegminal strut 1.1-1.3 mm long, endophallic
structure (3 specimens) 0.9-1.0 mm long. The spermatheca of the
paratype from Tuxtla Gutiérrez is shown in Fig. 123; the duct in this
specimen is 1.3 mm long and in the white female is 1.4 mm long.
H. brevicomus appears to be most closely related to aureus. With
aureus, brevicomus shares the elevated, often contiguous glabrous
areas of the elytra (but in aureus they are evenly distributed
dorsally and laterally), elevated bases of prothoracic setae (but in
aureus they are much more tuberculate), only 5 long erect setae on
Sutural interval on declivity of female (but these longer and
Straighnter in aureus), and similar male genitalia (but in aureus the
endophallic structure is straight proximally). H. aureus 7s known
only from Bolivia. D'Orbigny recorded aureus from "les mimosas" (see
Type Material of aureus); brevicomus was collected on Acacia. Both
sexes of aureus have a distinct tooth at the apex of the sutural
interval; in brevicomus there is no trace of a tooth in the male and
only a weak tooth in the female.
The name "brevicomus" means "short setae’, one of the most
distinctive external features of this species.
10. Hadromeropsis (Hadromeropsis) aureus (Blanchard)
Figs, 49, 51, 53, 92-94, 124; Map 4
Hadromerus aureus Blanchard, 1846:201. Type, female, labelled "7247,
on underside of green disc; "2248"; "P1.16 Fig.7" on vertical
label on pin; "Museum Paris, De Chiquitos, A. Mojos, D'orbigny
Howden: Hadromeropsis 45
1834"; and on green label in box "H. aureus Blanch. Bolivia, M.J.
'Orbigny" (Paris). See Type Material.
Diagnosis.-Clothed with scales which are yellowish with a metallic
lustre in teneral specimens (as the type), becoming white without any
metallic lustre in mature specimens; prothorax (Fig. 49) with random
glabrous spots ranging from elevated to pustulate; elytra (Fig. 51)
with larger glabrous areas, each area usually the entire width of the
interval, slightly convex, some areas confluent forming slender
sinuous subfasciae. Apex of elytra of male slightly produced into a
pair of blunt, divergent teeth (Fig. 53).
Description.-Male, length 8.9-9.2 mm, width 3.2-3.5 mm. Female,
length 8./-10.8 mm, width 3.5-4.3 mm. Color as in Diagnosis. Scales
especially dense around eye, in depressed areas of pronotum and on
elytra, often imbricate on the latter. Metepisternum sparsely scaled
and with a row of long, fine, white prostrate setae, the tip of one
overlapping the base of the succeeding one by 0.3-0.5. Setae of head,
rostrum, and prothorax appressed, as long as 1 scale. Rostrum 1.2x
longer than wide, dorso-lateral edges slightly elevated, parallel or
weakly convergent caudally. Epistoma occupying less than 0.3 of
anterior edge of rostrum, its apex marrow, rounded or acute.
Interantennal line faintly convex at most, rostrum feebly concave
caudad of interantennal line. Funicle with segment 2 averaging 1.3x
longer than segment 1. Prothorax (Fig. 49) 1.1x wider than long,
almost as wide at apical constriction as at basal constriction; disc
vaguely flattened or depressed either side of midline, these areas
densely squamose, remainder of disc with random bare spots as in
Diagnosis, occasional spots confluent. In profile, disc feebly convex
or flattened and apical constriction weakly to not at all impressed.
Elytra across humeri 1.2x wider than prothorax in male, 1.3-1.4x wider
in female; elytra 3.0x longer than prothorax in male, 3.2x longer in
female. Sides of elytra parallel basally, thence subparallel, very
weakly rounded to the weak apical umbone; apices of elytra of male
(Figs. 51, 53) divergent, sutural interval produced in a brief, blunt
tooth; apices of female produced in a pair of longer, parallel teeth.
Base of elytra straight. Declivity of male oblique, summit gradual;
declivity of female more abrupt, suture at summit with row of 4 or 5
much longer setae. Elytra with elevated glabrous areas as in
Diagnosis; each glabrous area with a long, fine seta near its caudal
edge, the setae of the apical half of elytral intervals 1, 3, and 5,
and the declivity longer and more erect than the setae of the basal
half. Striae distinct, punctures smaller than a single scale and
separated by width of 1-3 scales. Fore coxa without a tubercle but in
2 of 4 males examined with a feeble thickening at inner distal margin.
Fore femur of male 2-2.3x wider than hind femur; distally with a
moderate, thick flange on inner edge and a few weak tubercles below
tibial groove. Fore femur of female 1.5-1./7x wider than hind femur,
flange much less developed, tubercles absent. Fore tibia bowed
distally; distal tooth as long as 0.6-0.8 of apical width of tibia,
with a row of 8-10 small, blunt denticles on inner edge, these
obscured by long setae, especially in males. Ventrite 5 of male 2.3x
wider than long, rather evenly, sparsely squamose; apex broadly
emarginate. Ventrite 5 of female 1.8-2.0x wider at base than long;
triangular with apex briefly rounded; almost flat. Male genitalia as
46 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
in Figs. 92-94; aedeagus 2.4-2.6 mm long; aedeagal apodeme 1.1 mm long
(short in relation to length of aedeagus); tegminal strut 1.3-1.4 mm
long; flagellum 1.2-1.3 mm long, approximately 0.5 the length of the
aedeagus, stiff, heavily sclerotized, gradually tapering from base to
apex. Female with spermatheca as in Fig. 124, 0.8-0.9 mm _ long;
Spermathecal duct approximately 1.0 mm long, moderately sclerotized at
junction with bursa copulatrix.
Type Material.-Apparently described from the unique type in Paris,
a teneral female in excellent condition. The numbers on the labels of
the type refer to the manuscript catalogue of the d'Orbigny
collection: "Chiquitos, sur les mimosas a Santa Ana (Compicon?) 1834"
(H. Perrin, in litt.).
Distribution.-Map 4. BOLIVIA. La Paz: Chulumani, Coroico,
Nigrillani. Santa Cruz: Santa Ana in Chiquitos Prov.
Specimens were collected in January and August.
Specimens examined: 5 males, 9 females. Specimens in Auckland,
Dresden, London, Paris, Rosario de Lerma, Washington, Howden.
Remarks.-One female has some scales very pale green, especially on
intervals 6, 7, and 8, as if a vague remnant of an elytral vitta, and
indicating the possibility of all-green or green maculate specimens.
In addition to the diagnostic characters, aureus differs from
meridianus and gemmifer in the longer segment 2 of the funicle, more
strongly developed femoral flange, and mostly imbricate scales of
elytra. From cretatus, another all white species, aureus differs in
the prothoracic sculpture, strial punctures larger, setae of alternate
intervals longer, base of elytra straight, and apex of elytra
produced. See Remarks on brevicomus for additional comparisons.
The name aureus is appropriate for the type specimen which is
teneral and consequently golden, but “argenteus" which appears on the
Dresden specimens would better describe mature specimens.
11. Hadromeropsis (Hadromeropsis) cretatus (Champion)
Figs. 50, 52, 54, 95-97, 125; Map 3
Hadromerus cretatus Champion, 1911:184, Tab. 7, Fig. 31. Type,
female, labelled "Caldera, 1200 ft, Champion" (London). See Type
Material.
Diagnosis.-Densely clothed with imbricate, pure white scales, with
small glabrous spots randomly scattered over entire dorsum (Fig. 52);
the glabrous spots not elevated above scales and nowhere with
tubercles. Apices of elytra of male individually briefly rounded
(Fig. 52); apices of female with a sharp tooth concealed by long setae
(Fig. 54). Fore femur with very weak flange on inner edge distally.
Flagellum approximately twice as long as aedeagus, evenly sclerotized,
tapered to apex. Spermathecal duct 6.0-6.5 mm long.
Description.-Male, length 10.1-11.2 mm, width 3.9-4.4 mm. Female,
length 10.8-12 mm, width 4.6-5.0 mm. Color as in Diagnosis.
Rostrum broad, 1.1x or less longer than wide; obsoletely concave
(male) or flat (especially female); median line only obsoletely
impressed in one male, otherwise without sculpture. Dorso-lateral
edges of rostrum abrupt, prominent, convergent caudally; in dorsal
Howden: Hadromeropsis 47
view sides of rostrum including scrobe clearly visible. Epistoma
long, narrow, its apex vague, rounded; occupying less than 0.3 of
anterior edge of rostrum. Funicle with segment 2 averaging 1.4x
longer than segment 1. Prothorax in dorsal view 1.0-1.3x wider than
long; sides strongly, evenly rounded between constrictions; squamose
as in Diagnosis. In profile (Fig. 50) disc weakly convex, apical
constriction absent dorsally. Elytra across humeri 1.3x wider than
prothorax in male, 1.4x wider in female. Elytra 2.9x longer than
prothorax in male, 3.2x longer in female; sides parallel basally,
thence subparallel, very weakly rounded to the weak apical umbone;
apices of elytra as in Diagnosis. Base of elytra arcuately emarginate
between striae 5. Declivity very gradual; in female sutural interval
at summit of declivity with a row of 4-14 setae approximately 3x as
long as adjacent setae. Glabrous spots of elytra each with a single
seta not conspicuously longer or straighter on alternate intervals.
Strial punctures (Fig. 52) very small and inconspicuous; in abraded
areas a puncture seen to be smaller than the scar of a scale and very
shallow; punctures separated by 2-5 scales. Fore femur 2.1x wider
than hind femur in male, 1.6-1.8x wider in female; with very feeble
flange on inner edge distally. Fore tibia weakly bowed, similar to
that of rufipes (Fig. 72), distal tooth as long as width of apex in
male, slightly shorter in female; with a row of small teeth on inner
edge, with only a few minute tubercles on posterior surface distally.
Ventrite 5 of male 2-2.2x wider at base than long, rather evenly,
Sparsely squamose; apex broadly truncate. Last tergite of male
Slightly transversely flattened. Ventrite 5 of female 1.8-2.0x wider
at base than long, apex narrowly rounded; feebly convex. Male
genitalia as in Figs. 95-97 and Diagnosis; aedeagus 3.5-3.6 mm long;
aedeagal apodeme 1.9 mm long; tegminal strut 1.9-2.3 mm_ long;
flagellum 5.4-6.5 mm long. Female with spermatheca as in Fig. 125;
Spermathecal duct 6.0-6.5 mm long.
Type Material.-Described from a unique with the head slightly
deformed or injured in life over left eye.
Distribution.-Map 3. COSTA RICA. Alajuela: 1 male, Grecia, 14 May
1977, R. Campos (Howden). San José: 1 male, San José, Feb. 28, 1924,
Nevermann Coll. (Washington); 1 male, Monte Rey, Rfo Candelaria, 1946
(San José). No locality given: 1 male, 3 females, Septiembre, Paul
Serre (Paris, Howden); 1 male, 1 female (Cambridge). PANAMA. Chiriqui:
1 female, Caldera, 1200 ft., Champion (the type) (London).
Remarks.-Champion's description, "the rostrum canaliculate and
moderately excavate" might appear to contradict my description. His
“canaliculate" means the median line is finely impressed and his
"excavate" refers to the caudal margin of the epistoma. Except in two
males, the median line is not modified in any way; it is usually
completely covered with scales as well, though the scales may not
always be contiguous at the median line. Another point of confusion
is found in the "flattened, tuberculiform" glabrous spots of the
elytra; these spots are indeed flattened; in none of the specimens
examined did I see anything I would call tuberculiform.
On the abdomen and fore coxae of one female there are individual
Scattered iridescent green scales which are smaller than the white
scales.
The very distinctive habitus should make this species immediately
48 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
- recognizable. Within Central America, the only other white species is
gemmifer which has the fore coxa with a tubercle, fore tibia
tuberculate on posterior surface, female ventrite 5 notched apically
and genitalia very different.
12. Hadromeropsis (Hadromeropsis) rufipes (Champion)
Figs. 62, 72, 138, 367; Map 2
Hadromerus rufipes Champion, 1911:185; Tab. 7, Figs. 34, 34a. Type,
female, labelled "Costa Rica, P. Biolley,” “Arcangeles, 1500-1700
m.," "@" "Arcangeles 1200 m Lin pencil] 1192 Lin ink]" on folded
piece of paper, "Type’ on orange-ringed disc, "Sp. figured.,"
'B.C.A., Col., IV. pt. 3, Hadromerus rufipes, Ch." (London).
Diagnosis.-Based on female only. Very large. Apparently normally
covered with two sizes of scintillating green and some opalescent
scales, the larger scales forming a vitta on elytral interval 4 as
depicted by Champion (1911, Tab. 7, Fig. 34) as well as a vitta on
interval 8; both elytral vittae may be continuous with narrow vittae
On prothorax. Ventrite 5 (Fig. 138) smooth and polished medially,
rounded apically. Spermathecal duct 2.2 mm long.
Description.-Female, length 13.0-13.4 mm, width 5.0-5.2 mm.
Black, legs and antennae rufous. Normally covered with scales as in
Diagnosis; ventrally scales dense on sides of abdomen, mostly absent
on central half of ventrites 1 and 2, sparser and smaller on ventrites
3 and 4 centrally, sparse basally on ventrite 5, apical half of
ventrite 5 with only 1 scale; legs very sparsely clothed with small
scales. Rostrum with dorso-lateral edges basally indistinct, rounded;
edges apicad of interantennal line well defined, approximately
parallel. Surface of rostrum almost flat, median line finely
impressed between eyes; distal 0.3 of rostrum deflected, here very
slightly wider than long. Surface of head and rostrum with scattered
fine punctures which may be concealed by scales in fresh specimens.
Epistoma occupying 0.3 of anterior edge of rostrum, approximately as
wide as long, its distal emargination extending 0.3 of length of
epistoma. Segment 2 of funicle 1.1x longer than segment 1; club
2.6-2.8x longer than wide. Prothorax 1.2x wider than long, sides only
moderately rounded, slightly flattened dorso-laterally, large scales
thus protected from abrasion by the depression consequently forming a
vitta; in profile prothorax scarcely convex, apical constriction
absent, basal constriction very faint. Disc of prothorax medially
apparently naturally glabrous, smooth and _ polished. Setae of
prothorax very fine, as long as 1-2 scales, appressed(?). Scutellum
mostly glabrous with some small scales and setae. Elytra across
humeri 1.4-1.6x wider than prothorax. Elytra 3.8x longer’ than
prothorax. Base of elytra weakly produced or not between striae 5,
thence slightly obliquely deflected. Sides of elytra parallel for
basal 0.15, thence 1.1x wider than across humeri and parallel to
middie, thence very gradually convergent to apex, the apical umbone
scarcely to distinctly evident in outline. Elytral sutures briefly
divergent on declivity below erect setae, ending in weak to prominent
pair of diagonally directed teeth whose apices overlap (Fig. 62).
Howden: Hadromeropsis 49
Edge of elytra opposite ventrite 5 thickened and prominent, interval
10 depressed in this area and striae 9 and 10 here indistinct but
ending apically in several foveae which further emphasize the distal
tooth. Strial punctures very fine, smaller than a small scale. Setae
of elytra difficult to assess because of abrasion; apparently setae of
basal portion of intervals 3, 5, and 7 longer, as long as 2-3 of the
larger scales; all setae very fine and erect. Fore femur 1.3x wider
than hind femur, distal flange arcuate but weak. Fore tibia as in
Fig. 72 or apical edge with inner lobe as in micans (Fig. 70).
Ventrite 5 (Fig. 138) 1.8x wider than long, flat or feebly convex,
medially smooth and polished; rufous apex punctate. Spermatheca as in
Fig. 367; spermathecal duct 2.2 mm long (type not dissected).
Distribution.-Map 2. COSTA RICA. 1 female, "“Arcangeles", 1200-1700
m (London). 1 female, [San José] Escazf, Coll. Kuschel (Auckland).
Extensive questioning in Costa Rica and elsewhere was not
successful in locating "Arcangeles", but it was frequently suggested
that it is the name of a farm or estate.
Remarks.-Both specimens are abraded and the glabrous areas of the
elytra are covered with scars of small scales. The elytral vittae
should still be evident in fresher specimens because of the different
nature of the scales in the vittae - much larger and overlapping
compared to the scales of adjacent intervals.
H. cretatus also occurs in Costa Rica and resembles rufipes in the
very fine elytral punctures and occasionally bears scintillating green
scales on the ventral surface. Compared to cretatus, rufipes is
elongate, has a shorter second funicular segment, more attenuate
elytral apex, and much shorter spermathecal duct.
From at another large species possibly occurring in Costa
Rica, rufipes differs in the absolutely smooth, non-tuberculate
Surface of the prothorax and elytra and ventrite 5 rounded apically
instead of emarginate. The coxal tubercle is absent in rufipes but
the other characters are often more easily viewed.
13. Hadromeropsis (Hadromeropsis) superbus (Heller)
Figs. 2, 3, 98-100, 126; Map 4
Hadromerus superbus Heller, 1921:29. LECTOTYPE, HERE DESIGNATED, male,
labelled “Rep. ARGENTINA, Prov. Tucuman, II 1906, C. Bruch,"
"K.M. Heller," "Typus" on green rectangle with black border,
"Hadromerus superbus Heller i.1.," "Hadromerus superbus m. i. 1."
handwritten (Bruch Coll., Buenos Aires). See Type Material.
Diagnosis.-Clothed with iridescent green scales only or with both
green and lavender iridescent scales; prothorax with random glabrous
areas not elevated; elytra with random glabrous areas rectangular,
usually the entire width of an interval, scarcely elevated. Eye
flattened (Fig. 2). Prothorax (Fig. 2) much wider than long, sides
very strongly rounded.
Description.-Male, length 7.2-8.1 mm, width 2.8-3.0 mm. Female,
length £9 6 mm, width 3.1-3.8 mm. Vestiture as in Diagnosis.
Integument and scales very shiny, sometimes with golden lustre.
Lavender scales when present randomly interspersed with green scales
50 “ Contrib. Amer. Ente:Inst.:; volwcl9, no. 6, 1982
on head and prothorax; on elytra lavender scales concentrated on disc
and intervals 9 and 10 leaving intervals 7 and 8 entirely green; often
with a vague green pattern basally and medially. Rostrum with
dorso-lateral edges abrupt from apex to middle of eye, parallel or
Slightly bowed outward; sides perpendicular or concave between edge of
dorsum and scrobe and thus not visible from above; sides convex below
ventral margin of scrobe. Rostrum 1.2x longer than wide; dorsal
Surface shallowly concave; frons with a small interocular fovea;
median line glabrous. Epistoma occupying 0.3 of anterior edge of
rostrum. Funicle with segments 1 and 2 usually equal in length. Eye
as in Diagnosis and Fig. 2. Prothorax as in Diagnosis and Figs. 2, 3,
averaging 1.2x wider than long, convex, the apical constriction weak
dorsally. Postocular vibrissae arising from a small knob. Elytra
across humeri averaging 1.2x wider than prothorax in male, 1.3x wider
in female. Elytra of male and female averaging 3.0x longer than
prothorax. Shape of elytra as in Figs. 2, 3. Apices of elytra of
male conjointly rounded, with a minute tooth in some; in female with
small distinct tooth. Elytra with a single, fine seta arising from
each glabrous spot, the setae of alternate intervals erect on apical
half of elytra and much longer; setae much more numerous on sutural
interval on declivity, but not clustered there, all setae slightly
longer in female than in male. Strial punctures approximately as
large as a scale, separated by approximately one diameter. Fore femur
of male 2.0x wider than hind femur, fore femur of female 1.4-1.6x
wider than hind femur; inner edge both sexes with a brief arcuate
flange sometimes separated from femur by a crease, edge of flange with
a few minute tubercles, a few tubercles of same size below tibial
groove. Fore tibia bowed distally; distal tooth approximately 0.5 as
long as width of apex in male, shorter in female; inner edge with an
average of 10 small blunt denticles. Ventrite 5 of. male 2.1x wider
than long, apex truncate, edges deflected. Ventrite 5 of female
1./-1.8x wider at base than long, flattened, side edges deflected,
apex narrowly rounded. Male genitalia as in Figs. 98-100; aedeagus
1.5-2.1 mm long, aedeagal apodeme 0.9 mm long, tegminal strut 0.9-1.2
mm long, flagellum 1.6 mm long. Spermatheca as in Fig. 126;
Spermathecal duct 1.0-1.3 mm long.
Type Material .-PARALECTOTYPES, HERE DESIGNATED, 6 females: 1
female, labelled "Rep ARGENTINA, Prov. Tucuman, I 1906, C. Bruch"
(Buenos Aires); 1 female, labelled "Rep. ARGENTINA, Prov. Catamarca,
7.111.1907, C. Bruch," "Typus" on green rectangle, "Hadromerus
Superbus Heller" (Buenos Aires); 1 female, labelled "Rep. ARGENTINA,
Prov. Tucuman, 190 , C. Bruch," "1906, II," "“superbus TYPUS" on red
rectangle (Dresden); 2 females, labelled "Argentina, Prov. Salta, mir
1905, Steinbach" (Dresden); 1 female, labelled "Rep. ARGENTINA, Prov.
Cordoba, 189, C. Bruch", "Cotypus" (Paris). Heller does not list the
province of Catamarca but the specimen from there is considered a
paralectotype because it bears a type label.
Distribution.-Map 4. ARGENTINA. Catamarca. Cordoba: Alta Gracia,
La Granja, Quiscate. Jujuy: Ledesma. Salta: Cerrillos, Cerro San
Bernardo, La Merced, Salta, Vinaco (15 km S. £1 Carril). Santiago
del Estero. Tucumén.
Specimens were collected from December through March.
Specimens examined: 11 males, /2 females. Specimens in Auckland,
Berlin, Buenos Aires, Curitiba, Dresden, Paris, Washington, Howden.
Howden: Hadromeropsis 51
Remarks.-This is a very distinctive species, readily recognized by
the flattened eye alone. The green and lavender vestiture is likewise
unique but six specimens appeared oily and no color was present at
all, the specimens being a uniform dark brown.
Specimens which I collected were very lively and appeared quite
colonial. The five specimens taken at Vinaco were on one branch of
Mimosa farinosa Grisebach and landed on the beating’ sheet
Simultaneously. The 17 specimens from Cerrillos were taken on four
different days, all from one very large Prosopis chilensis (Md.)
Stuntz, mostly on one branch. At Cerro San Bernardo six specimens
were taken on Piptadenia macrocarpa Benth. and one very teneral
Specimen on herbaceous weeds.
The gemmifer Group
14, gemmifer (Boheman) 16. batesi n. sp.
15. meridianus n. sp.
Characteristics of Group.-Glabrous or densely clothed with scales,
elytra without color pattern except that formed by random bare spots
or more dense scales. Fore coxa with a tubercle on inner distal edge
Opposite trochanter (Fig. 57); tubercle less prominent in female (Fig.
5B) tubercle most readily observed from a caudal or oblique angle as
in the illustrations. Fore tibia of male on inner edge with a row of
cylindrical tubercles, in female these are more acute and flattened
like a tooth. Male with endophallic structure variable, flagellum
well developed or indistinct. Female without bursal sclerites.
Remarks.-The distinct coxal tubercle which characterizes this
group iS sometimes present in a greatly reduced state in aureus
(scintillans group) and in beverlyae (argentinensis group). The
tubercle is most strongly developed in gemmifer. This and the absence
of both a bursal sclerite and paired lateral sclerites in the female
definitely place ollltesc with the flagellate species in spite of the
indistinct flagellum.
In the three species in this group the fore tibia is bowed
distally, the distal tooth is long and acute, and the inner apical
lobe is moderate.
14. Hadromeropsis (Hadromeropsis) gemmifer (Boheman)
Figs. 6, 55-59, 61, 101-103, 127; Map 4
Hadromerus gemmifer Boheman, 1845:418. Faust, 1892:1; Champion,
1911:184. Type, female, labelled "Typus" on a red rectangle
outlined in black; "129" printed on white; "762" written on
white; "Hadromerus gemmifer, Reiche, Venezuela, Mannerheim"
written on white (Stockholm).
Hadromerus scabricollis Faust, 1892:1. LECTOTYPE, HERE DESIGNATED,
male, TabeTTed "Colonia Tovar, E. Simon, I.11.88," “Museum Paris,
Venezuela, Es simon 169y 7 "rouse Wet.” tear! Sr ne
handwritten on white, "Hadromerus scabricollis n. sp.," "TYPE"
printed on red (Paris). See Type Material. NEW SYNONYMY.
Se Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Diagnosis.-Glabrous, shiny black (84% of males, 20% of females) or
densely squamose with scales of iridescent or scintillating green (12%
of males, 38% of females), iridescent cupreous or mixed colors (1% of
males, 31% of females), or non-iridescent white or greenish (3% of
males, 11% of females). Elytra of male (Fig. 6) slightly wider across
humeri, tapering gradually to declivity, or parallel-sided. Female
with ventrite 5 distinctly notched at apex (Fig. 59). Aedeagus with
granules of dorsum extending onto sides distally. Internal sac (Figs.
101-102) with 2 pairs of inflatable lobes (only the dorso-lateral pair
spiculate), and one long ventral lobe, internally with ejaculatory
duct leading to a heavily sclerotized structure which forms the
ventral surface of a dorsal cupped lobe and beneath this with a short,
needle-like, free sclerite like a rudimentary flagellum. Spermatheca
with nodulus distinctly shorter than cornu (Fig. 127).
Description.-Male, length 8.5-12.3 mm, width 2.8-4.0 mm. Female,
length 70-15 DO. mm, owidth 3.6-573" 74m... Color’ ase.in Diagnosis;
naturally glabrous (i.e, not glabrous because of abrasion) specimens
with integument shiny and smooth, lacking scars of scales, but often
with a few minute iridescent scales especially in the depressions of
apex of elytra, and with occasional full-sized scales ventrally. All
with a dense patch of scales on hind coxa and in a metasternal spot
anteriorad to hind coxa. All sculpture stronger and more conspicuous
in glabrous specimens. Rostrum moderately broad (Figs. 55, 56)
ranging from flat (some females) to deeply triangularly concave;
median line varying from unimpressed to distinctly impressed between
eyes to their caudal margin. Epistoma long, narrow, occupying
approximately 0.3 of anterior edge of rostrum. Eye moderately large,
convex. Antennal funicle with segment 2 equal to or slightly longer
than segment 1. Prothorax of male almost spherical, as wide as long,
wider in female; evenly sculptured on disc and sides with faint to
strong, dense tubercles each with an inconspicuous recumbent seta at
its anterior edge, setae all directed toward middle of anterior margin
of prothorax. Scutellum with or without scales; densely clothed with
long, often broad, setae which may conceal the scales under them.
Elytra of male as in Diagnosis and Fig. 6. Elytra of male 1.1-1.2x
wider across humeri than across prothorax; elytra 2.5-3.0x longer than
prothorax. Elytra of female 1.26-1.4x wider across humeri than across
prothorax; elytra 3.0-3.3x longer than prothorax. Elytra of female
slightly wider at about middle. Strial punctures small, striae
regular but somewhat indistinct on declivity, this especially evident
in glabrous specimens. Intervals each with a sparse row of fine
setae, those of alternate intervals becoming longer and straighter
towards apex of elytra. Apical umbone weak. Declivity of male in
profile oblique, slightly concave or not; of female perpendicular or
almost, usually concave. Sutural interval at summit of declivity in
female only with very long, stout, horizontal setae. Apices of elytra
briefly individually rounded in male; in female, produced in a smal]
tooth approximately as long as a tarsal claw. Tubercle of fore coxa
well developed (Figs. 57, 58). Fore tibia of male on inner edge with
dense row of small, blunt teeth or elongate tubercles; posterior
surface (Fig. 61) with similar multiple blunt tubercles, especially
distally, the tubercles rapidly becoming smaller away from inner edge;
fore tibia of female with denticles of inner edge sparser, sharp,
Howden: Hadromeropsis a
without multiple tubercles posteriorly. Ventrally with very long,
fine setae on prosternum restricted to small median area. Ventrite 5
of male 1.8-2.0x wider across base than long, almost flat, apex
broadly truncate-emarginate, finely punctate apically. Ventrite 5 of
female as in Diagnosis and Fig. 59; 1.8-1.9x wider across base than
long, almost flat. Aedeagus ranging in length from 3.1-4.2 mn,
averaging 3.6 mm. Internal sac as in Figs. 101-103 and Diagnosis;
Spermatheca as in Diagnosis, Fig. 12/7; spermathecal duct 1-1.5 mm
Tong.
Type Material.-The lectotype designated for scabricollis Faust is
the only specimen labelled "Colonia Tovar, E. Simon” as in the
description. Three PARALECTOTYPES, HERE DESIGNATED, 1 male, labelled
"Columbia, Baden" and 2 females, labelled "Venezuela," all three
labelled "Type" on red paper and with a gold square in Dresden
apparently complete Faust's type series. The Simon collection was
acquired by the Paris Museum in 1897 which seems to explain the label
"J. Faust det. 1897," 5 years after the publication of the
description. The type locality was described by Simon in a discussion
of his three-month trip to Venezuela (1889:169-171).
Distribution.-Map 4. Central America and northern Colombia and
Venezuela between 1000 and 1800 m. GUATEMALA. Alta Verapaz: Baleu,
mcpio. San Cristobal Verapaz. COSTA RICA. “locality doubtful".
PANAMA. Darien. COLOMBIA. Cesar or Guajira ["Magdalena"] : Socorpa
Mission, Sierra de Perija. Cundinamarca: "Bogota." Norte de
Santander: eet e Magdalena: Rfo Frio, Cerro Patron. VENEZUELA.
Aragua: Choroni, Colonia Tovar, Rancho Grande. Distrito Federal:
Caracas, Caracas Valley, Parque Nacional Avila. Mérida. Miranda: £1
Hatillo, Nucleo E17 Laurel. Tachira: Cordero. Zulia: Maracaibo.
Specimens were collected in every month except February and March,
and have been taken on Bracatinga brasiliense, Cassia, Mimosa, and
peach foliage.
Specimens examined: 157 males, 198 females. Specimens are in most
collections studied.
Remarks.-This is a highly variable species superficially
resembling Hadrorestes in the characters of the vestiture and the
punctuation of striae 9 and 10 which are somewhat confused in glabrous
specimens but distinct in squamose specimens. The variation in the
concavity of the dorsal surface of the rostrum is so extreme, as is
the color, that specimens of gemmifer can look extremely. different.
Two specimens are a deep iridescent ultramarine and one is a uniform
non-metallic pastel green. One extreme male from Venezuela (Miranda)
has the prothorax wider than long and with faint lateral depressions
on the disc.
All the Central American and Sierra de Perija specimens (total of
25) are glabrous black and robust, but the single specimen from
Magdalena, the only record between these two areas is an iridescent
green male. H. gemmifer is the only predominantly black species in
North or Central America (but see rufipes).
54 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
15. Hadromeropsis (Hadromeropsis) meridianus n. sp.
Figs. 4, 5, 60, 104-107, 128, 129; Map 4
Diagnosis.-Similar to gemmifer, but: Male with sides of elytra not
tapered from humeri. Apical elytral umbone weaker in both sexes.
Female with apex of ventrite 5 rounded instead of emarginate.
Aedeagus with granules confined to dorsal surface; internally with
flagellum (Fig. 105) approximately as long as aedeagus. Spermatheca
(Figs. 128, 129) with nodulus long and straight, usually much longer
than cornu.
Description.-Holotype, male, length 9.8 mm, width 3.9 mm. Black,
densely clothed with scintillating green, often overlapping scales.
Scales not noticeably more dense on hind coxa; prothoracic tubercles
and random spots on elytra naturally glabrous. Rostrum 1.1x longer
than wide, with a triangular concavity basad of interantennal line,
the latter weakly but distinctly elevated; median line impressed
between anterior half of eyes. Antenna with segment 2 of funicle
equal to segment 1. Prothorax 1.2x wider than long, sides strongly
rounded between constrictions, sculpture consisting of very weak
setiferous tubercles as in gemmifer. Scutellum densely squamose with
overlapping scales. Elytra (Figs. 4, 5) as in gemmifer male, except
sides very slightly wider to and caudad of middle, summit of declivity
in profile very broadly arcuate, not abrupt as in Fig. 5, apical
umbone almost imperceptible, apices of elytra very briefly produced
into a knob. Fore coxal tubercle well developed. Fore femur 2.1x as
wide as hind femur. Fore tibia with tubercles of posterior surface
much less numerous than average gemmifer male, but more numerous than
in an extremely sparsely tuberculate gemmifer male. , Caudal surface of
ventrites 2, 3, and 4 perpendicular, approximately equal in height.
Antero-lateral corner of ventrites 4 and 5 with a deep pit. Ventrite
5 slightly convex, 2.1x wider at base than long, shorter and apex more
broadly emarginate than in gemmifer male. Aedeagus as in Diagnosis,
Fig. 104, 1.9 mm long; aedeagal apodeme 1.4 mm long; tegminal strut
1.9 mm long; internally with flagellum (Fig. 105) approximately 2.5 mm
long, strongly sclerotized .for proximal 0.3, distal remainder
filamentous.
Allotype, female, length 10.3 mm, width 4.0 mm. Like holotype,
except elytra in profile with disc evenly convex, highest at middle,
summit of declivity more distinct, declivity slightly oblique, not
concave; with elongate setae on sutural interval graduated in length,
not numerous. In dorsal view sides of elytra gradually convergent
from middie to apex, apices ending in a tooth shorter than the tarsal
claw. Fore leg as in gemmifer female; fore femur 1.6x wider than hind
femur. Ventrite 5 (Fig. 60) rounded at apex, 1.7x wider at base than
long. Spermatheca as in Diagnosis, similar to Fig. 128; spermathecal
duct 1.5 mm long.
Type Series.-Holotype, COLOMBIA, Cundinamarca, Monte Redondo nr.
Bogota, 1500-1600 m, VI.27.1947, L. Richter Coll., Frank Johnson Donor
(New York). Allotype, same data as type (New York). Paratypes, 8
males, 7 females. COLOMBIA. Cundinamarca: 6 males, 2 females, same
data as type or [1] 1400 m, VI.26.1947 (New York, Howden); 1 female,
Bogota, v. Lansberge (Leiden); 1 female, Cordillera de Subia between
Howden: Hadromeropsis 55
Bogota and Girardot, 2300 m, VII.24.1947, L. Richter Coll., Frank
Johnson Donor (New York); 1 male, Quetame, IX-44 (San Francisco).
Tolima: 1 male, 3 females, Ibague, Fr. Claver (Paris). BRAZIL. 1
female, Amaz., Bowring 63.47 (London).
Remarks.-The specimens from Ibague and “Amaz." are uniformly
larger (male, length 10.0 mm, width 3.6 mm; females, length 11.7-12.5
mm, width 4.9-5.2 mm) than the specimens with more explicit data from
Cundinamarca (males, length 8.5-10.4 mm, width 3.0-3.9 mm; females,
length 9.1-11.1 mm, width 3.6-4.1 mm). All specimens are densely
Squamose. The three males and two females that appear to be glabrous
as in the glabrous gemmifer are actually squamose when viewed under
Magnification, the scales being transparent due in part to a teneral
condition. The elytral shape of both sexes exhibits little variation
and is rather conspicuously different from that of gemmifer. The
aedeagus ranges in length from 2.4-3.0 mm (6 males dissected), thus
smaller and with no overlap in size with gemmifer. Other parts of the
male genitalia vary as follows: aedeagal apodeme 1.4-1.5 mm long,
tegminal strut 1.5-1.9 mm long, flagellum 2.0-2.7 mm long. Length of
Spermathecal duct is 1.3-1.5 mm long.
The spermathecal duct is scarcely modified in length,
approximately the same length as in gemmifer, and seems short for the
length of the flagellum. I interpret this not as a different system
from other flagellate species, but as evidence of recent change, a
view supported by the closeness of meridianus and gemmifer.
The name "meridianus" means southern and iTades to the range
being more southern than that of its sister species gemmifer.
16. Hadromeropsis (Hadromeropsis) batesi n. sp.
Figs. 63-65, 108-111, 130; Map 4
Diagnosis.-Rostrum (Fig. 63) long and dorsally narrow, the
dorso-lateral edges prominent (almost keeled) and convergent from apex
to head, the area between concave. Fore femur of male distally with
the posterior edge enlarged into an arcuate flange (Fig. 65).
Flagellum as long as or longer than aedeagus.
Description.-Holotype, male, length 11.4 mm, width 4.5 mm. Black,
densely clothed with scintillating green scales; disc and sides of
prothorax with small glabrous black areas; elytral intervals with
irregular, random glabrous areas occasionally confluent; all glabrous
areas of dorsum slightly elevated (squamose areas consequently
Slightly depressed), smooth and shiny, and with a single seta.
Rostrum as in Diagnosis, Fig. 63, 1.5x longer than width at
interantennal line, the dorso-lateral "keel" extending beyond anterior
edge of eye; in dorsal view, scrobes completely visible, dorsally
rostrum only about 0.8 ventral width. Mandibular scar very prominent
(Fig. 64). Epistoma occupying 0.3 of anterior edge of rostrum.
Antenna with segment 2 of funicle 1.7x longer than segment 1.
Prothorax 1.2x wider than long; sides strongly rounded, 1.4x wider
than basal constriction; 1.2x wider at basal constriction than at
apical constriction. Disc in profile with basal constriction strong,
56 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
apical constriction absent, thickest at basal 0./, feebly arcuate to
apex. Glabrous elevated spots of prothorax becoming weakly
tuberculate laterad, each with a very fine, short, inconspicuous,
recumbent seta; no other setae on disc or sides. Postocular vibrissae
very well developed, arising from a prominent knob. Scutellum densely
Squamose, without setae. Elytra across humeri 1.3x wider’ than
prothorax; elytra of paratypes averaging 2./x longer than prothorax,
sides almost parallel, apical umbone weak. Declivity gradual,
oblique. Apices of elytra unmodified. Glabrous spots on base of
elytra with minute, recumbent setae; apicad setae gradually becoming
erect, stiff, dark, but still fine, until all on declivity are erect;
summit of declivity without additional or longer setae. Fore coxa
with tubercle well developed, but left tubercle abraded in type. Fore
femur enormously thickened, 1.2x wider than head between outer edge of
eyes, 2./x wider than hind femur; with a brief arcuate flange on inner
edge distally and a few weak tubercles in tibial groove beside flange.
Distal end of fore femur (Diagnosis, Fig. 65) with posterior flange,
inner surface of flange with a few scales and setae. Fore tibia
proximally peculiarly flattened and twisted downward (Fig. 65); inner
edge with 9 small, blunt teeth (or elongate tubercles); distally with
a posterior lobe similar to but smaller than that of beverlyae.
Ventrite 5 broadly truncate-emarginate at apex, 2.0-2.2x wider than
long in paratypes. Genitalia as in (Figs. 108-111); aedeagus 3.2 mm
long; flagellum (Fig. 108, 110) as long as aedeagus. Spiculum
gastrale as in Fig. 111; apex of spiculum gastrale in ventral view
with stalked sclerites arising from first connecting membrane as in
Fig. 109 (see Remarks under genus).
Allotype, female, length 12.3 mm, width 5.1 mm.’ Differs from type
as follows. Occasional scales, especially on fore legs, vivid blue.
Segment 2 of funicle 1.4x longer than segment 1. Prothorax 1.3x wider
than basal constriction. Elytra 1.4x wider across humeri_ than
prothorax; elytra 3.1x longer than prothorax; sides of elytra only
Slightly wider medially than in type, apical umbone scarcely stronger
than in type; sutural interval below summit of declivity with 6 dark
setae of increasing then decreasing length; apex of sutural interval
attenuated into brief tooth. Fore femur 0.8x as wide as head between
outer edge of eyes, 1.5x as wide as hind femur; flange of inner edge
greatly reduced and tubercles absent; without flange on distal end of
fore femur. Fore tibia unmodified proximally; inner edge with 5
small, sharp teeth and several denticles; posterior lobe absent.
Caudal surface of ventrites 2, 3, and 4 equal in height. Ventrite 5
triangular, 2x as wide at base as long, very weakly convex, apex
rounded. Spermatheca of paratypes as in Fig. 130, nodulus slightly
deflected; spermathecal duct 1./-2.0 mm long, sinuous and much wider
at bursa copulatrix.
Type Series.-Holotype, BRAZIL, Para, Santarém (Cambridge).
Allotype, BRAZIL, Santarém, 151 (Washington). Paratypes, 36 males, 16
females. BOLIVIA. Pando: 1 male, 1 female, Tambopatha Hath, Lat. 13°
5', Long. 69° GR, CapLitainles Mailles & Vincent, 1914 Aoflt (Paris).
BRAZIL. No other data: 1 female, Bates (London); 2 males, 1 female,
E.A. Klages Coll. (Ithaca); 1 male, Lower Amazon (Ithaca). Minas
Gerais: 1 male, Ponte Nova, May, 1899 (SG Paulo). Para: No other
data, 2 males (London); 1 female, Santarem, Coll. Kuschel (Auckland);
Howden: Hadromeropsis 57
2 females, Santarem (Washington); 1 male, Santarem, Amazonas,
Staudinger and Bang-Haas (Eberswalde); 20 males, 6 females, Santarem,
Klages Coll'n Exotic Coleop. Acc. No. 2275 or 2966 (Pittsburgh,
Howden); 1 male, Tapajos (London). PERU. 1 female, Chaquimayo, Coll.
Kuschel (Auckland). Locality unknown or questionable: 2 males
(Cambridge); 1 male, "Costa Rica"* (London); 4 males, 3 females,
"Panama"** (4) F. Psota Coll. (Chicago, Howden).
* The Costa Rica label is identical to some which are labelled
"Locality doubtful."
** This could be Panema, a Bates collecting area near Santarém,
improperly transcribed to Panama (Bates, 1910:189). The Psota
Collection locality labels are often incorrect and Panama being so far
Out of the documented range of batesi, the Costa Rica and Panama
localities are questionable.
Remarks.-Males vary in length from 8.5-11.2 mm and in width from
3.3-4.4 mm. Females vary in length from 9.6-13.5 mm and in width from
4.1-5.5 mm. The rostrum is consistently long and narrow facilitating
quick identification of batesi among the many green species. The
female specimen from Peru is 13.5 mm long, 1.5 mm longer than any
Other female. It also differs in the color of the scales of the fore
tibia which are a vivid lavender. The only other obvious variation in
the paratypes is in the degree of development of the fore femur of the
male. In the least developed, it is 2.3x wider than the hind femur
and the distal flange is also much smaller.
This spectacular species is named in honor of Henry Walter Bates,
who collected at least one of the above paratypes, and to commemorate
his 11 years spent collecting specimens and recording “aspects of
nature under the equator" (Bates, 1910, Title page).
The argentinensis and nobilitatus Groups
These two groups represent subdivisions of a unit and the groupings
are primarily for the taxonomist's convenience. In both groups the
internal sac of the aedeagus has patches of spicules, spiculate
inflatable lobes, a very heavy internal sclerite which’ is
condyle-shaped at its anterior (proximal) end, a dorsal inflatable
cupped lobe near the proximal end of the internal sclerite, and the
apex of the internal sac membranous. Females of the species have a
complex, somewhat funnel-shaped sclerotization inside the bursa
copulatrix at the end of the spermathecal duct; spermathecal duct
moderate in length, spermatheca in one plane except nodulus slightly
angled in fasciatus. The vagina in all species has longitudinal faint
to moderate sclerotized lines (Figs. 182, 188).
The groups do not readily lend themselves to interpretation from
museum specimens only. Apparently the disruption of the habitat of
the coastal Brazilian forests is reflected in confusing phenotypes.
In several instances in the nobilitatus and argentinensis groups, a
more northern taxon has a Santa Catarina form which is morphologically
different and more subdued in color.
58 Contrib. Amer: Ent. Inst., vol 19, no. 6, 1982
The argentinensis Group
17. togatus (Boheman) 21. pallidus n. sp.
18. argentinensis (Hustache) 22. speculifer n. sp.
19. plebeius n. sp. 23. beverlyae n. sp.
20. pulverulentus n. sp.
Characteristics of Group.-Metallic lustre infrequent. Elytra
without tubercles except plebeius and beverlyae. Fore femur without
flange on inner edge diet y except beverlyae. Fore tibia almost
Straight. Female ventrite 5 smooth and highly polished in many
species. Internal sac of male with ventral plate absent, or present
but not free, forming a bottom to the sac, or present but not
sclerotized.
Remarks.-H. argentinensis is associated with thorn scrub,
beverlyae with cerrado; the remainder appear to have ranges roughly
corresponding with coastal forest formations of Brazil and are often
sympatric with nobilitatus group species.
17. Hadromeropsis (Hadromeropsis) togatus (Boheman)
Figs. 13, 159, 160, 184; Map 5
Hadromerus togatus Boheman, 1840:290. Type, female, labelled
Brasilia, Westin" printed on white paper; "Typus" on red
rectangle bordered in black (Schoenherr coll., Stockholm).
Hadromerus brachispinosus Boheman, 1840:291. LECTOTYPE, °° HERE
DESIGNATED, rare, labelled with small green triangle with no
inscription; ‘"Hadr. brachispinosus Chevr. Brasil. Germar"
written in black on white (Schoenherr coll., Stockholm). See
Type Material. NEW SYNONYMY.
Diagnosis.-Moderate to large size. Elytra of female (Fig. 13)
covered with a conspicuous anchor-shaped dark mark sharply defined in
white; remainder of elytra ochraceous, white, pale olive or moss
green, or obscure; with or without green or rosy lustre; declivity
with a dark spot _on apical umbone. Elytra of male with same anchor
pattern evident or confused by random clusters of scales alternating
with glabrous spots creating a tessellate appearance. Apex of rostrum
and epistoma "normal", i.e., anterior corners of epistoma not produced
in a lobe. Glabrous spots of elytra at most weakly convex, never
tuberculate. Edge of elytra smooth with no trace of tubercles.
Description.-Male, length 9.5-11.4 mm, width 3.3-4.0 mm. Female,
length 11.0-14.2 mm, width 4.0-5.3 mm. Elytra patterned as in
Diagnosis and Fig. 13. White or ochraceous scales dense, imbricate
around eye, continuing along side of head and side of prothorax to
base of elytra from interval 4 over and under humerus and continuing
thence into the elytral pattern, these markings vague in male, very
sharply defined in female. Elytra of male with glabrous areas often
the full width of interval and sometimes confluent; apical umbone not
always with glabrous spot. Dorsal surface of male and female head,
rostrum, dark central area of pronotum, and elytral anchor mark
sparsely clothed with scales which under the microscope appear weakly
to strongly iridescent green, faintly cupreous, or non-iridescent.
Howden: Hadromeropsis 59
Rostrum approximately as long as wide, flat or (rarely) feebly concave
in male, median line briefly impressed basally; sides parallel or
apically divergent; surface sparsely punctate. Setae of head and
rostrum slender, as long as 1.5-2 scales, recumbent. Epistoma
occupying 0.28-0.3/ of anterior edge of rostrum, epistoma very
slightly ogival. Prothorax 1.0-1.1x wider than long, sides weakly to
moderately rounded between constrictions; apical constriction obsolete
dorsally; female especially with vague flattened areas on disc on
either side of median line. Pronotum smooth medially or with
setiferous arcuate pustules and other low convexities; glabrous
setiferous spots sparser on sides because of denser scales, spots
pustulate, setae as long as 1-2 scales. Elytra across humeri 1.3x
wider than prothorax in male, 1.3-1.4x wider in female. Elytra
averaging 3.0x longer than prothorax in male, 3.3-3.6x longer in
female. Elytra in dorsal view with sides parallel for basal 0.16,
thence gradually divergent to beyond middle where they average 1.1x
wider than across humeri in both sexes, gradually rounded to apical
-umbone which enters dorsal outline; apex usually broadly rounded in
male, interval 10 at apex slightly thickened and often briefly
horizontally flared posteriorly; apex of female and some males
slightly elongated triangular. Female apex of each sutural interval
thickened in a vertical lobe; apical modification densely pilose in
both sexes. Setae of elytra fine, straight; recumbent, semi-erect or
perpendicular; recumbent setae as long as 1 scale, semi-erect and
erect setae up to 2 scale lengths (posture and length of setae
possibly artifacts of abrasion); setae longer on base, sides and
declivity; female on sutural interval at summit of declivity with a
cluster of up to 12 very long setae. Legs, metasternum, and abdomen
with many fine, long setae in male; in female setae much sparser,
shorter, curved. Fore femur 1./7-2.0x as wide as hind femur in male,
1.6x in female; faintly pustulate and sometimes rugulose distally.
Fore tibia bowed distally; distal tooth averaging 0.5x as long as apex
of fore tibia; apex posteriorly with edge expanded into a lobe the
size of the outer dorsal lobe; posterior surface with numerous
granules or small acute tubercles near teeth of inner edge, granules
most numerous in well-developed males, sometimes absent in female.
Male ventrite 5 across base 1.6-1.8x wider than long; almost flat;
almost evenly squamose; with moderate, sparse punctures; apex narrowly
emarginate. Female caudal surface of ventrites 2, 3, and 4 equal,
perpendicular, margin evenly arcuate; perpendicular surface of
ventrite 2 vertically striate. Female ventrite 5 across base 1./-1.9x
wider than long, almost flat, scales sparser or absent medially.
Aedeagus as in Fig. 160. Internal sac as in Fig. 159, differing from
similar species in the pair of small fused sclerites at extreme apex
ventrally. Spermatheca as in Fig. 184.
Type Material.-PARALECTOTYPES of Hadromerus brachispinosus
Boheman, HERE DESIGNATED, 2 males: 1 male, labelled, “Brazil; orange
Square with a gritty black texture on top, white underside; "Coll.
Chevrol."; "Cotypus" on red rectangle with black border (Schoenherr
coll., Stockholm). 1 male, with no labels but listed as "Hadromerus
brachispinosis Schonherr (Brasilia)" (Chevrolat coll., Stockholm).
Distribution.-Map 5. BRAZIL. Minas Gerais: Faz. dos Campos. Rio
de Janeiro: Nova Friburgo, Rio de Janeiro. Rio Grande do Sul (?).
60 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Santa Catarina: Cauna, Corup4, Mafra, Rio Natal, Rio Vermelho. Sao
Paulo: Pindamonhangaba. PARAGUAY. Alto Parana: Hohenau.
Specimens were collected in January, February, and September
through December.
Specimens examined: 13 males, 35 females. Specimens in Auckland,
Cambridge, Curitiba, Dresden, London, New York, Oxford, Paris, Sao
Paulo, Stockholm, Washington, Howden.
Remarks.-From the few specimens available there is an indication
that scales with metallic green iridescence in both sexes occur in the
northern part of the range only, not in Santa Catarina.
The male labelled "Rio Grande" is very similar to the Rio Vermelho
male suggesting that this locality is in the state of Rio Grande do
Sul. Both specimens are very fresh with the vestiture in good
condition; all elytral setae are erect and nearly perpendicular.
The ventral lobe and granules on the posterior surface of the male
fore tibia are developed about half as much as in the extreme
beverlyae.
One male had an obsolete flange on the fore femur which is an
important diagnostic character of nobilitatus. The lack of tubercles
on the elytra, especially the apical edge, should distinguish togatus
from nobilitatus at a glance.
The anchor-shaped elytral mark is diagnostic and very uniform, the
only deviation being one in which the fascia is almost bisected on
interval 6 and another in which it is terminated at interval /7.
18. Hadromeropsis (Hadromeropsis) argentinensis (Hustache)
Figs. 7-10, 161, 162, 181, 182; Map 5
Hadromorus [sic] argentinensis Hustache, 1928:157; P1.5, Fig. 2.
LECTOTYPE, HERE DESIGNATED, female, labelled "Alta Gracia La
Granja, Sierras de Cordoba, C. Bruch leg."; "Foto" printed on
green; "Typus" printed on green paper; “Hadromerus argentinensis
Hust." printed by hand on white rectangle with fine red border
(Bruch coll., Buenos Aires). See Type Material.
Diagnosis.-Elytra with a dark, mostly glabrous postmedian spot on
intervals 5, 6, and 7. Rostrum with very few rounded scales on side
below scrobe, no rounded scales on ventral surface of rostrum. Elytra
short and thick (Figs. 7, 8), convex in profile (Figs. 9, 10), apex
not or scarcely extended in dorsal view. Elytra without an apical
umbone, i.e., intervals 5 and 6 at their apical termination not at all
elevated. Ventrite 4 of female with caudal surface perpendicular,
straight; ventrite 5 of female glabrous and polished medially. Sexes
very similar.
Description.-Male, length 5.3-7.4 mm, width 2.0-3.0 mm. Female,
length 6.2-8.6 mm, width 2.6-3.6 mm. Males from Uruguay as short as
4.6 mm, females as short as 6 mm. Integument brown to black. Clothed
with white, tan and obscure scales, the latter rarely with green,
lavender or cupreous reflections; scales sometimes gray-blue or
gray-green in teneral specimens. Side of prothorax with a vitta of
dense white or white and tan scales extending from eye to humerus.
Ventrally with scales tan, mostly concentrated on sides; ventrites 3,
Howden: Hadromeropsis 61
4, and 5 with very few scales and these only on the extreme lateral
edges. Rostrum with dorsal surface more or less flat, dorso-lateral
edges not acute, sides broadly visible from above. Surface of head
and rostrum with punctures approximately the size of a scale, these
often changing to rugae on rostrum. Median line broadly, evenly
impressed from between eyes almost to apex of epistoma, frontal fovea
obsolete to deep. Epistoma occupying .36-.45 of anterior edge of
rostrum; anterior edge of rostrum at margin of epistoma slightly
produced. Outer contour of mandible rounded; scar small and
elliptical, not protuberant. Ventral surface of head and rostrum
usually with no rounded scales. Prothorax averaging 1.1x (1.09-1.2x)
wider than long; dorsal and apical constrictions strong, equal; apical
constriction obsolete dorsally; in profile, convex to slightly convex.
Disc of prothorax sparsely scaled, sparsely punctate, the glabrous
areas smooth and polished. Elytra across humeri averaging 1.3x wider
than prothorax in male, 1.4x in female. Elytra averaging 2./7x longer
than prothorax in male, 3.0x in female. Form of elytra as in
Diagnosis and Figs. 7-10. Elytral intervals with random stiff blunt
setae, as long as 1-3 scales; those of apical half of elytra in
females especially much more nearly perpendicular and_ longer.
Infrequently summit of declivity in female with setae up to 5
scale-lengths. Apices of elytra conjointly rounded in male, in female
produced in a weak tooth. Fore femur in male averaging 1./x, in
female 1.6x wider than hind femur; with longitudinal rugae distally.
Fore tibia on outer edge covered with scales smaller than those of
body, anterior and posterior surfaces indistinctly rugose, with some
granules near teeth on inner edge. Distal tooth of fore tibia very
small, never exceeding the tuft of setae; female with a pair of distal
teeth. Ventrite 5 of male 2.0-2.2x wider than long, weakly convex or
not, apex truncate or truncate-emarginate. Ventrite 5 of female as in
Diagnosis, 1.8x wider than long, the flat polished surface sometimes
depressed below sides; apex broadly rounded. Male genitalia as in
Figs. 161, 162. Female genitalia as in Figs. 181, 182 (setae omitted
in drawings).
Type Material .-PARALECTOTYPES, HERE DESIGNATED, 1 male, 2 females,
labeTIed "Alta Gracia La Granja, Sierras de Cordoba, C. Bruch leg.,"
"30." in faded ink on pink square (Hustache Coll., Paris), these 3
Specimens mounted on individual cards on a single pin, the pin also
bearing a label "TYPE" printed in red on a rectangle; 1 male, 2
females, labelled "Rep. Argentina, Pr. Santiago del Estero, 190, C.
Bruch" (1 male, 1 female, Buenos Aires; 1 female, Paris, also labelled
"30." as the 3 paralectotypes from Alta Gracia).
Distribution.-Map 5. South of the Tropic of Capricorn § in
Argentina, Paraguay, Uruguay and Brazil. ARGENTINA. Buenos Aires:
Isla Martin Garcia; San Fernando. C6rdoba: Alta Gracia, Anizacate,
Capilla del Monte. Entre Rfos: Gualeguaychu, 54 mi E. Parana, Santa
Elena. Jujuy: Juancito. Misionés: Loreto. Salta: 4 km S. Campo
Quijano, Cerrillos, Cerro San Bernardo, Las Cafias, Metan, Rosario de
Lerma, Vifaco (15 km S. El Carril). Santa Fe: La Gallareta, Tartagal.
Santiago del Estero: Averfas, 25 km NW Icafio. Tucum&n: Chuscha,
Ciudacita, Tapia. BRAZIL. (Most specimens no other data. Santa
Catarina. PARAGUAY. Itapu& Hepua. URUGUAY. Canelones. Colonia:
Carmelo, Colonia. Montevideo. Paysando: Puerto Pepe Ajf. Soriano:
62 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Arroyo Colol6.
Specimens were collected in January through July, but were most
common in February and March.
Specimens examined. 215 males, 149 females. Specimens in
Auckland, Berlin, Buenos Aires, Cambridge, Curitiba, Dresden,
Eberswalde, Ithaca, London, Maracay, New York, Paris, Sao Paulo,
Tucumén, Washington, Howden, Wibmer.
Remarks.-Specimens from Sierras de COrdoba, the type locality,
exhibit most of the range of variation noted within the species. The
principal geographic variation seems to be the smaller size of
Specimens from Uruguay and contiguous areas of Argentina (Provinces of
Buenos Aires and Entre Rfos and Misionés Ter.). Specimens from Brazil
(21) average much larger.
Additional variation is as follows. One specimen had no dark
elytral spot but the area was sharply delimited by white scales so
that the pattern was still similar. In a male from Salta the dark
elytral spot was reduced to interval 5 only. Interval 9 of the elytra
may occasionally have some setae set on weak tubercles in males and
females. Ventrite 5 of the male had up to 26 scales per side;
ventrite 5 in the female usually had no scales but as many as six were
seen on one side.
I did not see the specimen mentioned by Hustache (1928:157) from
"Alto Paran&, Misiones (Wagner)" with the golden yellow vestiture. It
is possibly only a teneral specimen.
Although apparently very distinctive in appearance, small
specimens of this species can still be readily mistaken for atomarius,
and larger specimens can be confused with plebeius. From atomarius,
argentinensis may be distinguished by the straight fore tibia; the
Shorter ventrite 5 of the male; elongate, cylindrical endophallic
apex; straight edge of ventrite 4 of female, and glabrous ventrite 5
of female. From plebeius, argentinensis differs in the absence of
round scales on the ventral surface of the rostrum, stout fore femur,
rounded exterior outline of mandible, shorter elytra without tubercles
and lack of an apical umbone.
According to Bruch (Hayward, 1960:18) the Jarvae of H.
argentinensis attack "los espinelles" (Acacia caven (Mol.) and Mimosa
scabrella Benth.). Data on specimens includes Acacia caven (in Entre
Rios) and Prosopis (in COrdoba). Hustache (1938:6) Tists specimens
from Loreto, Misionés, on Mimosa bracatinga. In the Province of
Salta, I took argentinensis by beating the foliage of Acacia
macracantha H.B. ex Willd., Mimosa farinosa Grisebach, Prosopis
chilensis (Mol.) Stuntz, and Mimosa strigillosa Torr. and ar.;
occasional specimens were found on tall weeds and one weevil was found
buried in the flower of Mimosa strigillosa. In Cérdoba at Capilla del
Monte argentinensis were common on Acacia caven (Mol.), small trees in
a pasture yielding 10 to 15 specimens each.
19, Hadromeropsis (Hadromeropsis) plebeius n. sp.
Figs. 15-17, 147, 164, 186; Map 5
Diagnosis.-Color pattern (Figs. 15-17) similar to that of
Howden: Hadromeropsis 63
argentinensis in the conspicuous dark spot on intervals 5, 6, and /.
Without a metallic lustre. Elytra with setae of intervals fine,
"erect", i.e., at an angle greater than 45° to surface; each seta set
On glabrous, flat to tuberculate spot. Apical umbone of elytra with 1
Or more glabrous tubercles. Fore femur slender; fore tibia almost
straight to weakly bowed, distal tooth very small and concealed by
dense setae. Apex of internal sac elongate (Fig. 164), with 2 pairs
of basal lobes not present in argentinensis.
Description.-Holotype, male, Jength 9.0 mm, width 3.3 mm.
Integument piceous, clothed with white, tan and obscure scales, the
white scales usually imbricate, the tan appearing ochraceous in some
lights and usually not imbricate. Head, rostrum, thorax, legs and
ventral surface clothed with random tan scales. Elytra patterned as
follows: with dark spots caused by combination of glabrous areas and
obscure scales, (1) on base of intervals 3 and 4, (2) in conspicuous
spot on intervals 5, 6, and 7 as in argentinensis, connected to suture
by zigzag line, and (3) on apical umbone; confused white vitta on
basal third of intervals 5 and 6 and white fascia across apical third;
center of disc with mixed white and tan; elytra overall with random
glabrous spots flat or elevated as in description of elytra below.
Rostrum 1.1x longer than wide, almost flat, dorso-lateral edges not
acute, the sides not quite vertical. Surface of head with punctures
approximately the size of a scale, changing to rugae on rostrum.
Median line impressed from frons almost to apex of epistoma. Epistoma
occupying approximately 0.3 of anterior edge of rostrum, anterior edge
of rostrum at epistoma slightly produced; epistoma 1.3x longer than
wide. Scales of side of rostrum rounded, changing to elongate
ventrally, on ventral surface of rostrum only a central triangular
area without scales. Prothorax 1.1x wider than long, sides moderately
rounded between constrictions, apical constriction obsolete dorsally;
in profile disc almost flat. Setae of sides of prothorax set on weak
pustules. Disc of pronotum slightly irregular, sparsely punctate,
surface polished between scales. Elytra as in Diagnosis and Fig. 15.
Elytra across humeri 1.4x wider than prothorax. Elytra 2.9x longer
than prothorax. Setae of disc of elytra (between striae 7 from basal
0.16 to declivity) arising from flat to slightly convex surface,
remainder of setae set on tubercles, those of declivity very small,
some no larger than a scale. Setae of elytra straight, most held at
an angle greater than 45°; longer than 2 scales. Setae on disc of
elytra colored testaceous or darker; setae on extreme base of elytra
and intervals 8, 9, and 10 paler or white. Apices of elytra briefly
divergent, thickened, densely clothed with fine setae. Edge of elytra
around ventrite 5 weakly, minutely tuberculate, appearing crenulate.
Fore femur 2.0x wider than hind femur, surface indistinctly
sculptured. Fore tibia slightly bowed from distal 0.25, surfaces with
moderate, confused sculpture; posteriorly with granules near inner
edge, inner edge with about 10 small teeth; distal tooth as small as
those along edge, completely concealed in dense fine setae. Central
0.3 of ventrites 3, 4, and 5 without scales. Ventrite 5 across base
2.0x wider than long; weakly convex; apex truncate. Genitalia as in
pe 164, 165; internal sac with spiculate part of apex especially
ong.
Allotype, female, length 9.4 mm, width 3.8 mm. Differs from type
64 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
as follows. White scales of elytra more condensed, forming a basal
arc, an oblique fascia from basal third to suture at middle, and a
wider apical fascia. Rostrum more robust. Epistoma 1.1x longer than
wide. Prothorax 1.2x wider than long, sides more strongly rounded,
surface smoother. Elytra 3.3x longer than prothorax. Elytra as in
Figs. 16, 17, 147. Apical umbone less prominent; apex more elongate,
ending in short, caudally directed tooth. Setae longer, mostly
perpendicular; 6 or 7 setae on sutural interval at summit of declivity
much longer. Edge of elytra not crenulate. Fore femur 1.5x wider
than hind femur. Caudal surface of ventrites 2, 3, and 4 straight,
perpendicular; in caudal view slightly arcuate. Surface of ventrites
3 and 4 flat, the caudal elevation beginning abruptly across middle of
segment. Scales of ventrites 3, 4, and 5 elongate, limited to extreme
sides. Ventrite 5 flat, smooth and polished except at sides; 1.8x
wider than long; apex narrowly rounded. Spermatheca as in Fig. 186.
Type Series.-Holotype, BRAZIL, Parana, Q. d'Agua, Rolando, 4-44,
1296, Colecao F. Justus Jor (Curitiba). Allotype, same data as type
(Curitiba). Paratypes, 6 males, 14 females. BRAZIL. Parana: 1
female, 5041, Gregorio Bondar Collection, David Rockefeller Donor (New
York); 1 female, Guarauna, 12.40, 1295, Colecdo F. Justus Jor
(Howden); 1 female, Ortogueira, 1-44, 1295, Colegdo F. Justus Jor
Curitiba). Santa Catarina: 3 males, 9 females, Nova Teutonia, 300-500
We QT 1h B52 28h TIE O45, 18. 1VG 1948, 1 19S, | 6.3 .1951, TT. 79665
11.1974, 11.1976 [2], 111.1977 [2], V.1977, Fritz Plaumann (Auckland,
Curitiba, S2o Paulo, Hespenheide, Howden). Sao Paulo: 1 male,
Staudinger (Dresden); 1 male, 1 female, Cantareira, 13.3.38, Dr. Nick,
Coll. Kuschel (Auckland).
Remarks.-Males vary in length from 8.9-9.1 mm and in width from
3.3-3.5 mm. Females vary in length from 7.7-10.7 mm and in width from
3.1-4.5 mm. Minimum color pattern includes the dark somewhat
cordiform scutellar area, the postmedian spot on intervals 5, 6, and
7, a dark spot on apical third of interval 2, and at least one
glabrous tubercle on apical umbone. The pattern can appear quite
different if the postmedian mark is continuous and forms a broad
common fascia as in fasciatus. Some pastel blue-green scales are
found on two male paratypes on the abdomen where they are randomly
interspersed with tan scales, and they are also found on two female
paratypes where they replace a few or most of the white scales of the
elytra. Ventrally in both sexes scales are limited to the sides of
the abdomen except ventrite 2 which may be squamose across entire
caudal edge; in the type, however, there is a single scale in the
center of ventrite 5. The apex of the rostrum of the female may be
produced at the outer edges and at the corners of the epistoma almost
as much as in fasciatus, but pterygia have not developed. The
prothorax of male paratypes is narrower, 1.05-1.09x wider than long.
In four males the apices of the elytra are prolonged into a short
tooth. Ventrite 5. of females ranges from 1.7-2.0x wider than long,
but in most females is 1.8x.
Both fasciatus and nobilitatus have setiferous tubercles on the
elytra as in plebeius; plebeius can be quickly distinguished from both
by the lack of a metallic lustre and short distal tibial tooth as wel]
as the other diagnostic characters.
Because it lacks the golden lustre of nobilitatus and the red
Howden: Hadromeropsis 65
lustre of female fasciatus, this species is called "plebeius, '
plebeian.
meaning
20. Hadromeropsis (Hadromeropsis) pulverulentus n. sp.
Figs. 12, 148-150, 163, 183; Map 6
Diagnosis.-Small; male, length 5.0-6.3 mm, female 6.4-8.0 mm.
rostrum (Fig. 149) as wide as long. Epistoma wider than long. Elytra
without tubercles; strial punctures usually foveate (Fig. 150); apex
of elytra rounded in male, attenuate in female (Fig. 148); setae of
edge of apical half of elytra, declivity, and lateral intervals very
long and conspicuous. Aedeagus (Fig. 163) almost evenly cylindrical.
Description.-Holotype, male, length 6.3 mm, width 2.2 mm.
Integument red-brown, metasternum and ventrites 1 and 2 almost black,
ventrites 3 and 4 paler than 1 and 2, ventrite 5 paler than elytra.
Without metallic lustre. Sparsely clothed with white and pale tan
scales arranged in a faint pattern of (1) a white vitta along base of
interval 4 joined across suture in an arc at basal fourth, and (2) a
small dark diamond on suture at summit of declivity forming a "V" with
a pair of dark spots on intervals 4 and 5 at middle. Scales denser
around eye, on side of head, and side of prothorax to humerus.
Rostrum as in Diagnosis and Fig. 149, dorso-lateral edges parallel,
dorsal surface slightly concave; median line sharply impressed from
between caudal edge of eyes to interantennal line, thence shallowly
concave to apex of epistoma. Epistoma 1.6x wider than long, occupying
0.47 of anterior edge of rostrum, sides of epistoma slightly arcuate,
anterior corners not produced. Sculpture of head and rostrum similar
to that of nobilitatus. Prothorax 1.04x wider than long, sides
moderately rounded between equal basal and apical constrictions. Each
seta of disc set in a puncture, those of sides of prothorax set on a
weak granule. Scutellum with several fine appressed setae, no scales.
Elytra as in Diagnosis; elytra across humeri 1.3x wider’ than
prothorax. Elytra 2./x longer than prothorax. Elytra with sides
Subparallel, very slightly wider (1.09x) at middle, apical umbone very
weak, apex rounded beyond umbone. Strial punctures foveate, larger
than in Fig. 150 of allotype, gradually becoming smaller on declivity;
on disc foveae separated by approximately their own diameter both
longitudinally and transversely. Setae of disc very fine and
inconspicuous; setae suddenly longer on sides and declivity from
apical 0.25, longest setae (on interval 10 apically) as long as 3
scales; only those setae caudad of apical umbone and on edge of elytra
around ventrite 5 straight, erect and conspicuous; sutural interval on
declivity with evenly spaced, curved setae as long as 2 scales. Fore
femur 1.4x wider than hind femur, without distal flange, without
sculpture except for a few rugulae distally. Fore tibia almost
Straight, teeth of inner edge minute, distal tooth as long as 0.32x
the width of tibia at apex. Ventrites 3, 4, and 5 without scales
medially; ventrite 5 across base 2.1x wider than long, moderately
convex, its apex broadly truncate, emarginate. Aedeagus as _ in
Diagnosis, Fig. 163; internal sac not extracted.
Allotype, female, length 6.1 mm, width 2.3 mm. Differs from type
66 Contrib. Amer. Ent.cinst,; vol. 19, no. 6, 1982
as follows. Elytral pattern much more distinct (Fig. 12), the basal
vittae enclosing a dark postscutellar spot and the apical ‘V" very
broad and conspicuous. Rostrum less concave. Epistoma 1.3x wider
than long, occupying 0.45 of anterior edge of rostrum. Prothorax
1.05x wider than long. Elytra across humeri 1.3x wider than
prothorax. Elytra 3.3x longer than prothorax. Sides of elytra gently
rounded at middle where they are only 1.2x wider than across humeri,
apical umbone weak, apex elongate; sutural interval attenuated into a
long tooth directed slightly inward and ventrad (Fig. 148). Lateral
edge of elytra somewhat constricted from ventrite 3 to apex; ventrites
3, 4, and 5 consequently narrow. Strial foveae smaller (Fig. 150).
Flytral setae longer and more erect, the longest as long as 4 scales;
setae of apical half of lateral intervals almost perpendicular to
surface and creating a bristly effect; only 2 setae on _ sutural
interval on declivity greatly elongate. Fore femur 1.5x wider than
hind femur. Teeth of inner edge of fore tibia and distal tooth short,
as long as 0.24 of width of fore tibia. Caudal surface of ventrite 4
perpendicular, its. edge evenly arcuate in caudal view. Ventrite 5
across base 1.6x wider than long, triangular, apex narrowly rounded;
surface almost flat, medially polished and with only a few minute
setae. Genitalia as in Fig. 183 but sclerotized streaks of vagina and
setae not shown.
Type Series.-Holotype, BRAZIL, Minas Gerais, Ouro Preto, Topazios,
22. 1T A562 J. Bechyné col. (S& Paulo). Allotype, same data as type
(Howden). Paratypes, 2 males, 6 females. BRAZIL. 1 female, no other
data, ex coll. Oberthur (Paris). Minas Gerais: 1 male, 1 female,
Bowring 63-47, longulus (Jek.) (London); 1 female, Coll. Kuschel
(Auckland). LOCALITY UNKNOWN. 1 female, Gorham Collection, acc.
68498, lentus, Jekel collection (Washington); 1 female, Bowring 63-47
(London); 1 female, Sharp Coll 1905-313, Hadromerus pulverulentus Jek
Aes SP. oo hes Columb ato: (hondon); cl (oumalepsohes9, Bowring»: 63245
pulverulentus (Jek), Bogota* (London).
*In view of the accurate data on the Minas Gerais specimens, the
"Columbia" and "Bogota" on these old specimens need to be
substantiated.
Remarks.-The two male paratypes are 5.0 and 6.3 mm long, 2.0 and
2.3 mm wide. Females are 6.4-8.0 mm long, 2.5-3.2 mm wide. In most
paratypes the color pattern on the elytra is much less developed than
in the type and allotype. In a teneral female the white scales on the
sides of the prothorax are slightly opalescent. In one of the two
males, the rostrum is almost flat. The elytral setae in several
females are much more conspicuous, longer and more erect; on the
sutural interval on the declivity, 0 to 3 setae may be greatly
elongated. The strial punctures are not foveate in the largest female
paratype; it is possible that the size of these punctures varies in
inverse proportion to the size of the specimen. In females the
perpendicular portion of the caudal surface of ventrite 4 varies from
the full width of the ventrite as in the allotype to only the central
0.6, and the angle varies from perpendicular as in the allotype to
slightly posteriorly projecting. The internal sac was not extracted
from any of the males.
H. pulverulentus may always be distinguished by the wide epistoma
and almost evenly cylindrical aedeagus. The elongate habitus, small
Howden: Hadromeropsis 6/7
size and bristly lateral setae will also separate the species but
these characteristics are more subjective and vulnerable to wear and
poor condition of specimens.
Note that the glabrous elytral spot when present is on intervals 4
and 5 or 4, 5, and 6 compared to a more lateral position in plebeius
and argentinensis.
For this species, I chose the Jekel manuscript name
"pulverulentus' meaning "dusty" since it describes nicely the
appearance caused by the pale scales scattered over the surface.
21. Hadromeropsis (Hadromeropsis) pallidus n. sp.
Figs: 20¢ 214/161, 166. 26/<:7167;. Map.6
Diagnosis.-Densely clothed with tan or grayish and white scales,
elytra with a white pattern as in Figs. 20, 21; or with a vittate
_ pattern formed of medial and apical fasciae abbreviated and connected
to basal mark. Head and rostrum robust (Fig. 151); dorso-lateral
edges of rostrum ill-defined, broadly rounded, especially basally.
Setae of dorsum of elytra white, parallel-sided, truncate at apex,
erect, scarcely curved. Female ventrite 5 weakly convex medially with
setae and sometimes scales medially. Male ventrite 5 evenly punctate.
Aedeagus short, in profile thick distally (Fig. 166); internal sac as
in Fig. 167 or with internal sclerite reduced.
Description.-Holotype, male, length 6.8 mm, width 2.5 mm.
Integument piceous. Scales tan and off-white, the latter often with
weak metallic green lustre. Most tan scales very evenly spaced, not
quite touching; tan scales sparser along median line of prothorax, the
glabrous area thus forming a dark vitta. Elytra with dark vitta on
interval 3 basally and a small, dark "V" on intervals 1-3 before
declivity; these dark areas formed by tan scales sparser and some
scales replaced with obscure scales. Whitish scales often imbricate;
whitish pattern of ring around eye continuous with lateral vitta on
prothorax and elytra to apical umbone; disc of elytra with vittate
pattern as in Diagnosis. Elytral intervals with 7-10 random glabrous
areas the size of 1-2 scales, each as convex as a scale, each bearing
an erect seta. Rostrum as in Diagnosis and Fig. 151, approximately as
long as wide; median line impressed from between eyes to interantennal
line; each longitudinal half of dorsal surface of rostrum
longitudinally convex to median line. Epistoma approximately as wide
as long, 0.3x as wide as anterior edge of rostrum. Scar of mandibular
Cusp slightly produced. Surface of head and rostrum with prostrate
setae as long as 1.5-2 scales, arising from minute punctures in smal]
glabrous spaces between scales, surface otherwise not sculptured.
Prothorax almost as long as wide, sides weakly rounded between weak
apical and basal constrictions; surface without evident sculpture. In
profile pronotum almost flat, basal constriction narrow, anterior edge
produced more than is usual in the genus. All setae of prothorax
prostrate, on disc as long as 1-1.5 scales, on sides as long as 2
scales. Scutellum with 1 seta-like scale, and several minute,
prostrate setae. Elytra across humeri 1.3x wider than prothorax.
Elytra 2.8x longer than prothorax. Elytra in dorsal view with sides
68 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
parallel for basal 0.2, thence very slightly, gradually arcuate,
widest at middle, apical umbone weak but distinct in outline, apex
beyond broadly rounded; apices unmodified. In profile summit of
declivity unmarked. Strial punctures fine, inconspicuous. Intervals
as wide as 4-5 scales, sutural interval narrower. Setae of elytra as
in Diagnosis, as long as 3-4 scales. Fore femur 1.5x wider than hind
femur, apparently without microsculpture. Fore tibia straight to
distal 0.2 thence very weakly bowed; inner edge with 8 small teeth;
distal tooth as long as 0.25 width of tibia at apex. Abdomen with
scales almost evenly distributed on ventrites 1 and 2, absent medially
on ventrites 3 and 4, slightly sparser medially on ventrite 9.
Ventrite 5 across base 2.0x wider than long, moderately convex, its
apex briefly emarginate, surface evenly punctate. Aedeagus as in
Diagnosis, Fig. 166. Internal sac similar to Fig. 167 but internal
sclerite greatly reduced to approximately one-third; spiculate apex of
sac shorter.
Allotype, female, length 6.5 mm, width 2.8 mm. Differs from type
as follows. Rostrum flatter, epistoma 1.2x longer than wide.
Protnhorax 1.2x wider than long. Elytra 3.0x longer than prothorax.
Elytra similar to Figs. 20, 21, but humeri Jess prominent and sutural
tooth much shorter. Fore femur 1.2x wider than hind femur. Fore
tibia with distal tooth single, as holotype. Ventrites 1 and 2 almost
evenly squamose, ventrites 3 and 4 medially with no round scales but
with appressed setae or seta-like scales. Caudal surface of ventrite
4 perpendicular; slightly, evenly arcuate from extreme sides.
Ventrite 5 across base 1.5x wider than long, scales absent on weakly
convex median area. Spermatheca resembling that .of pulverulentus in
Fig. 183; spermathecal duct 1.2 mm long.
Type Series.-Holotype, ARGENTINA, Misionés, Obera, 10.5.47,
Wittmer Teg., Kuschel Coll. (Auckland). Allotype, same data as type
(Auckland). Paratypes, 4 males, 1 female. ARGENTINA. Misiones: 1
male (Buenos Aires). BRAZIL. Minas Gerais: 1 male, Vila Monte Verde,
8.111.1972, J. Halik, 12383 (Sao Paulo). PARAGUAY. Alto Parana: 2
males, Hohenau, 12.1939, Hans Jacob leg. (Auckland, Howden). URUGUAY.
Montevideo: 1 female, So Amer Paras Lab, No. 298, 6-1-43, Berry
(Washington).
Remarks.-Males vary in length from 5.8-7.5 mm and in width from
2.2-2.7 mm. The female paratype is 10.0 mm long, 4.1 mm wide. The
specimens from Brazil and Uruguay have the elytra patterned as in
Figs. 20, 21; those from Argentina and Paraguay have the vittate
pattern. The male from Minas Gerais differs from the other males as
follows: integument. black but appendages paler, elytra flatter,
intervals as wide as 5-7 scales, setae of elytra shorter, apices of
elytra developed into a pair of divergent teeth or conical tubercles,
internal sac as in Fig. 16/7.
The internal sac in the four males dissected exhibits more than
the usual amount of variation. In one male from Paraguay the internal
sclerites are approximately midway between the small extreme of the
type from Misiones and the large extreme of the paratype from Minas
Gerais (Fig. 167). In the same male from Paraguay there is a slight
sclerotization of the ventral surface of the apex reminiscent of
speculifer.
It could be debated whether the blunt apex of the elytral setae is
Howden: Hadromeropsis 69
natural or a consequence of a filamentous tip breaking off. I feel it
is natural because all setae on the disc of the elytra are blunt but
the setae on the apical edges of the elytra are gradually tapered.
This holds true for teneral as well as older specimens. Likewise the
setae of the thorax, head and rostrum are almost as blunt, but their
apices are protected by their prostrate position.
In addition to the diagnostic characters given, the profile of the
elytra is distinctive in the unmarked summit of the declivity.
The name pallidus refers to the pale color of the specimens.
22. Hadromeropsis (Hadromeropsis) speculifer n. sp.
Figs. 11, 140, 143, 168, 169, 185; Map 7
Diagnosis.-Usually with a greenish or rosy metallic lustre.
Elytra immaculate or with a maximum pattern of elongate basal ring
between striae 1 and 5, an acute V-shaped fascia beginning at middle
and a similar postmedian fascia parallel to it, the latter two fasciae
sometimes joined laterally (Fig. 11). Elytra without tubercles or
pustules. Female with lateral edges of elytra strongly constricted
Opposite ventrites 3, 4, and 5; in ventral view (Fig. 143) sides of
elytra broadly visible. Female ventrite 4 with caudal surface
perpendicular, edge straight or appearing feebly emarginate. Female
ventrite 5 flat, medially mirror-like, highly polished, smooth,
without scales, with several short setae at most; laterally ventrite 5
with numerous setae, with or without scales. Aedeagus slightly
thicker distally; internal sac as in Fig. 168.
Description.-Holotype, male, length 6.1 mm, width 2.1 = mm.
Integument black. Rather densely covered with scales which are mostly
contiguous on dorsal surface, the random bare areas causing a slightly
tessellate appearance. Scales of side of rostrum little different
from those of dorsum, continuing onto ventral surface of rostrun,
absent on only central 0.4. Prothorax subvittate: scales sparser and
smaller along median line, condensed on either side of median line and
on sides. Scales on elytra leaving random naturally glabrous areas
approximately the size of a scale on base of elytra, becoming width of
interval by middle of elytra. Scales pale, opalescent, with strong
lavender and rosy metallic lustre. Rostrum flat, 1.1x longer than
wide; dorso-lateral edges well defined but not acute, slightly
inwardly arcuate; median line sharply impressed from between eyes to
interantennal line. Epistoma as wide as long, occupying .3/7 of
anterior edge of rostrum. Head and rostrum very sparsely, finely
setate-punctate. Prothorax 1.0/x wider than long, sides weakly
rounded between equal basal and apical constrictions; in profile
prothorax almost flat. Bare spots of prothorax approximately as
convex as adjacent scales, setae arising from these very
inconspicuous, prostrate, shorter than an adjacent scale on disc;
setae of sides only slightly longer. Scutellum with 9 seta-like
scales. Elytra across humeri 1.2x wider than prothorax. Elytra 2.6x
longer than prothorax. Elytra 2.3x longer than width across humeri.
Elytra in dorsal view with sides subparallel, very slightly wider
across middle, apical umbone weak, just entering dorsal outline, apex
70 Contrib. Amer. Ent. Inst., voretl9, no. 6, 1982
beyond broadly rounded; apices very briefly divergent, ending in a
blunt tooth. Strial punctures fine, elongate, except larger on
intervals 5 and 6 basally. Intervals basally as wide as 2-3 scales,
rapidly becoming as wide as 3-4 scales. Setae of basal half of elytra
very inconspicuous, as long as one scale; laterally and apically
changing to arched, then straight, becoming as long as 4 scales on
edge of elytra around ventrite 5. Fore femur 1.8x wider than hind
femur; sculpture obsolete. Fore tibia (Fig. 140) straight except
distal 0.23 slightly bowed inwards; inner edge with 7 small denticles;
distal tooth small, as long as 0.3x width of apex. Metasternum 1.15x
longer than ventrite 1. Ventrites 3, 4, and 5 with dense patch of
scales on extreme side, scales absent medially; entire abdomen
sparsely, evenly clothed with fine setae as long as those of apical
edge of elytra. Ventrite 5 across base 1.8x wider than long; medially
impunctate, without scales, with very few setae; apex truncate.
Aedeagus and internal sac of paratypes (type not dissected) as in
Figs. 168, 169. Aedeagal apodeme very short, 0.2-0.36x as long as
aedeagus.
Allotype, female, length 8.1 mm, width 3.2 mm. Differs from type
as follows. Scales distinctly tan and white with rosy and green
lustre; elytra with maximum pattern as described in Diagnosis.
Rostrum approximately as wide as long. Prothorax 1.02x wider than
long. Scutellum with 3 normal scales in addition to seta-like scales.
Elytra as in Diagnosis, Figs. 11, 143. Elytra across humeri 1.4x
wider than prothorax. Elytra 3.1x longer than prothorax. Elytra 2.2x
longer than width across humeri. Elytra in dorsal view with sides
gradually divergent to middie where they are 1.3x wider than across
humeri, thence rounded to interval 3, apex elongate, sutural interval
elongated into a short tooth; at apex interval 10 and edge of elytra
expanded before sutural tooth. Intervals much wider, from middle all
intervals except sutural interval as wide as 6 scales. Setae around
apical edge of elytra as long as up to 6 scales; sutural interval on
declivity with 3 long, stiff setae. Fore femur 1.3x wider than hind
femur. Apex of fore tibia with 2 very small teeth concealed in the
setae. Ventrite 1, 1.2x longer than metasternum. Abdomen as in
Diagnosis and Fig. 143. Ventrite 5 across base 1.6x wider than long.
Spermatheca as in Fig. 185.
Type Series.-Holotype, BRAZIL, Sao Paulo, Campos Jorddo,
11.1V.1962, E. Halik 2510 (S8 Paulo). Allotype, same data as type
but 12.1V.1962, 19921, Brazil Halik 1966 Collection laperatti ngkon
Paratypes, 1/7 males, 14 females. BRAZIL. Minas Gerais: 1 male, 2
females, Serra do Caraga, II1.1963, F. Werner, U. Martins, L. Silva
(S80 Paulo); 1 female, Serra do Caraga, 24.11-3.111.1972, Exp. MZUSP
(S80 Paulo); 5 males, 6 females, Vila Monte Verde, 16.1V.1960, 17 .196
Qik 18. 19608 Pade ncsl.196la; 28eIN1964 (P2}s Oebt 2965629,
15.111.1966, 17.111.1966, J. Halik (S&o Paulo, Washington, Howden).
Santa Catarina: 1 male, Rio Vermelho, II1.1947, A. Maller Coll., Frank
Johnson Donor (New York). S&o Paulo: 9 males, 3 females, Campos
Jordaos: 122 1V. 0962: (625 12;1V 59062 642° JP Mal iks) (S300 Pawo)
Washington, Howden); 1 male, 2 females, Campos Jordao, 12.2.52,
Wittmer leg., Coll. Kuschel (Auckland).
Remarks.-Males vary in length from 5.1-7.3 mm and in width from
2.0-2.7 mm. Females vary in length from 6.3-8.5 mm and in width from
Howden: Hadromeropsis 71
2.4-3.3 mm. The apex of the elytra is rounded and without a tooth in
half the males. In males the metasternum is 1.09-1.2x longer than
ventrite 1; in females ventrite 1 is 1.0-1.2x longer than the
metasternum. Ventrite 5 of females sometimes has a few scales at the
extreme lateral edges. Ventrite 5 of males has a few scales medially
in half the specimens, none in the others; at most it is sparsely,
minutely punctulate.
The internal parts of most of the type series were hard and did
not respond to softening techniques (see Methods). The male genitalia
shown (Figs. 168, 169) are from a specimen from Rio Natal, Santa
Catarina. The genitalia of the single dissectable male from the type
locality are apparently identical to that in the figures.
Hadromeropsis from the state of Santa Catarina which agree with
the “diagnostic characters .of . speculifer as listed» here «are
consistently different from those from the states of Sado Paulo and
Minas Gerais, an exception being one of two males from Rio Vermelho.
Compared to typical specimens, these Santa Catarina specimens differ
as follows. Size larger: males, length 7.3-/7./7 mm, width 2.5-2.8 mm;
females, length 7.8-9.0 mm, width 2.8-3.5 mm. Very densely squamose,
glabrous spots smaller, prothorax only obsoletely subvittate, median
line of rostrum completely or almost concealed by scales. Sometimes
(both males, 1 female) immaculate; metallic lustre weaker. Rostrum
1.3x longer than wide in male, 1.2-1.4x in female, dorso-lateral edges
converging apically. Prothorax as wide as long in male, 1.2x wider
than long in female. Elytra across humeri 1.3-1.4x wider than
prothorax in male, 1.4-1.5x wider in female. Elytra 2.9x longer than
prothorax in male, 3.1-3.3x wider in female. Intervals as wide as 8
scales. Elytral setae more conspicuous in profile. Fore femur of
female 1.6x wider than hind femur. Male metasternum 1.4x longer than
ventrite 1; female ventrite 1, 1.03-1.14 longer than metasternum.
Male ventrite 5 evenly, sparsely squamose and punctate.
The Santa Catarina specimens are labelled as follows: 3 females,
no additional data, A. Maller, Gregorio Bondar Collection, David
Rockefeller Donor (New York); 2 females, Cauna, I11.1945, A. Maller
Coll., Frank Johnson Donor (New York); 1 male, Joinville, 49.0W, 26.0S
sea-level, Aug. 1926, Antonio Maller, B.M. 1931-106 (London); 1
female, Mafra, Mall. (Paris); 1 female, Mafra, 800m, 12.65 (Curitiba);
1 male, Rio Natal, I1.1945, A. Maller Coll., Frank Johnson Donor (New
York); 1 male, 1 female, Rio Vermelho, XI1.1946, II11.1947, A. Maller,
Frank Johnson Donor (New York).
Field study is needed to determine if these Santa Catarina
Specimens represent extreme geographic variation or a sibling species.
Females of speculifer are especially recognizable by the strongly
contracted sides of the elytra around ventrites 3, 4, and 5 and by
the flat, mirror-like ventrite 5. Both sexes can be separated from
other species within its range as follows: from atomarius by the
straight fore tibia and absence of elytral tubercles; from
ulverulentus by the narrower epistoma (no wider than long) and finely
punctured striae; from plebeius by the lack of elytral tubercles,
smaller size, and very different color pattern; from pallidus by the
well-defined dorso-lateral edges of the rostrum.
The mirror-like surface of ventrite 5 in the female inspired the
name speculifer meaning "with a mirror’.
2 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
23. Hadromeropsis (Hadromeropsis) beverlyae n. sp.
Figs. 22-25, 152, 154, 156, 170, 171, 188-190; Map 6
Diagnosis.-Densely clothed dorsally with green scales, ventrally
and laterally with cupreous or golden scales. Anterior edge of
rostrum at margin of epistoma flared upwards and outwards (Fig. 156).
Both sexes with the glabrous spots of the basal half of elytral
interval 9 tuberculate, in dorsal view their profile more prominent
than the tubercles of the sides of the prothorax. Fore femur of male
with very small, shiny tubercles or granules along entire inner
surface including the arcuate distal flange of inner edge (Fig. 152).
Apical end of fore tibia in both sexes produced in a rounded lobe on
posterior edge, the lobe at least as long as the distal tooth (Fig.
154); apical end of fore tibia of opalinus (Fig. 153) shows usual
condition in other species.
Description.-Holotype, male, length 7.9 mm, width 3.3 mm. Dorsal
surface of rostrum, head, prothorax, elytra, and fore femur densely
clothed with green scales which exhibit a golden lustre in certain
lights; remainder of body including elytral intervals 8, 9, and 10
with cupreous scales with golden lustre. Scales of basal half of
elytral intervals 4 and 7 slightly more dense giving a subvittate
appearance. Prothorax and elytra with random, small, glabrous spots
approximately the size of a scale; the single minute seta of each
glabrous spot on dorsal surface recumbent, very inconspicuous;
glabrous spots of side of prothorax and basal half of elytral interval
9 tuberculate, in dorsal view those of interval 9 more prominent in
profile than those of sides of prothorax. Rostrum 1.2x longer than
wide, dorsal surface approximately parallel-sided, feebly depressed
medially, median line impressed between anterior half of eyes.
Epistoma occupying approximately 0.5x of anterior edge of rostrum,
strongly concave, its apex rounded; epistoma as wide as long; sides of
epistoma from about middle becoming carinate then keeled and flared
outward and upward (Fig. 156). Mandibular scar scarcely exceeding
Outline of mandible. Protnhorax 1.2x wider than long; sides strongly
rounded; basal and apical constrictions equal; apical constriction
weak dorsally. Basal constriction with a few white, curved setae from
ventral surface evident in dorsal view. Elytra (Fig. 22) across
humeri 1.2x wider than prothorax; elytra 2.8x longer than prothorax;
sides very slightly divergent to middle, thence very gradually
convergent to apex, apical umbone very weak, sutural interval briefly
attenuate to form tooth. In profile (Fig. 23) summit of declivity
unmarked, elytra gradually deflected from about middle to apex, all
glabrous spots of declivity including sutural interval set with short
(about as long as 2 scales), straight, obliquely deflected setae.
Ventral surface of entire body (except ventrites 3, 4, and 5) and all
legs with the long, wispy setae particularly dense. Fore coxa on
inner distal edge with trace of tubercle as in gemmifer. Fore femur
as in Diagnosis and Fig. 152, 2.6x wider than hind femur, slightly
narrower than head between outer edges of eyes, scales absent on inner
granular area. Fore tibia as in Diagnosis and Figs. 152, 154; inner
edge with cylindrical tubercles, similar smaller tubercles covering
much of inner surface. Abdomen with scales sparse on ventrites 2 and
Howden: Hadromeropsis 73
5 medially, absent medially on ventrites 1, 3, and 4. Ventrite 5
across base 2x wider than long, apex broadly truncate, weakly convex.
Aedeagus as in Fig. 1/1; internal sac as in Fig. 1/70, without basal
ventral lobes.
Allotype, female, length 9.3 mm, width 3.7 mm. Differs from type
as follows. Rostrum 1.1x longer than wide. Elytra (Figs. 24, 25)
across humeri 1.4x wider than across prothorax, sides wider at middle,
apex only slightly more attenuate and apical umbone only slightly more
prominent. Long, wispy setae of ventral surface replaced by shorter,
Curved setae. Fore leg with no trace of tubercle on fore coxa;
granules of fore femur and flange greatly reduced; tibia with granules
reduced; lobe of posterior apical edge of tibia shorter. Ventrites 3
and 4 with no scales on central third, the glabrous surface roughly
sculptured; surface flat, rising abruptly to caudal margin. Ventrite
5 flat, 1.9x wider than long; medially glabrous and polished,
laterally bordered with short white setae and with a small sublateral
patch of elongate scales; apex truncate. Genitalia of paratypes as in
Figs. 188-190; vagina with 8 faint, long fins.
Type Series.-Holotype, BRAZIL, Distrito Federal, 20 kmN Brasilia,
11110-1970, 1250 m, JM & BA Campbell (Sao Paulo). Allotype, same
data as type (Sao Paulo). Paratypes, 9 males, 10 females, same data
as type (Ottawa, Howden).
Remarks.-Males vary in length from 7.4-9.0 mm, and in width from
2.8-3.4 mm. Females vary in length from 7.4-9.3 mm, and in width from
3.1-3.9 mm. The subvittate appearance is very consistent, as is the
Character of the glabrous spots: mostly uniserial, larger on basal
half of the elytra, becoming smaller apically until smaller than a
Single scale; females usually more densely squamose. The type series
1s very uniform except for one aberrant male which has the median line
impressed on the disc of the prothorax, the head protuberant, and the
basal half of interval 9 of the right elytron only raised, its scales
elongate and two of the tubercles bearing moderately long, curved
setae. Most specimens do not have even a trace of the coxal tubercle.
The green dorsal surface and cupreous sides and venter must lend
this species particularly good color camouflage against green foliage
and the reddish soil of its cerrado habitat.
It gives me great pleasure to name this species in honor of Mrs.
Beverly Ann Campbell of Ottawa who collected the entire type series.
The nobilitatus Group
24. nobilitatus (Gyllenhal) 26. excubitor n. sp.
25. atomarius (Boheman) 27. fasciatus (Lucas)
Characteristics of Group.-Often with a complex fasciate color
pattern on the elytra which is similar in the two sexes or reduced
(weaker) in the males of some species; with a strong to weak
(according to the species) red or golden lustre in reflected light.
Segments 1 and 2 of antennal funicle very long, equal in length.
Elytra often with setiferous tubercles. Fore tibia bowed distally;
distal tooth of female double in many species. Internal sac of
aedeagus ventrally with a heavily sclerotized plate which is free at
its distal end (e.g., Fig. 174), this plate absent in fasciatus (Fig.
74 Contrib. Amer, Ent. Inst., vol. 19, no. 6, 1982
. BOF.
24. Hadromeropsis (Hadromeropsis) nobilitatus (Gy]lenhal )
Figs. 1, 14, 173, 174, 191-194; Map 8
Hadromerus nobilitatus Gyllenhal, in Schoenherr, 1834:128. Type,
female, labelled "Brasilia, F....Lillegible]" written on white
paper; "TYPUS" on red rectangle with black border (Schoenherr
Collection, Stockholm).
Hadromeropsis similis Hustache, 1938:6. Type, female, labelled
Republic Argne., Rio Parana, Territoire des Missiones,"
"Hadromeropsis similis m.," "TYPE" in red ink on white rectangle
(Hustache Collection, Paris). Synonymized by Kuschel, 1955:278.
Diagnosis.-Body with a golden or reddish metallic lustre. Elytra
(Fig. 7 marked with (a). circumscutellar half circle originating at
base of interval 4, (b). oblique fascia from basal third to middle at
stria 1 or suture, (c). common "V" with its apex at summit of
declivity; these markings creamy white or tan in female, light to dark
ochraceous in male; area between markings with scales. smaller,
lavender or green under microscope, this area obscure macroscopically.
Prothorax with sides moderately to strongly rounded. Setiferous
tubercles of intervals 8 and 9 conspicuous dorsally. Male: fore femur
with distinct flange; distal tooth of fore tibia approximately as long
as width of tibia at apex, acute. Female: fore femur with flange
obsolete; distal tooth of fore tibia shorter, approximately 0.3-0.5x
width of tibia, usually single. Fore tibia both sexes abruptly bowed
at distal 0.25; of equal width to apex. Female caudal margin of
ventrite 4 usually arcuate medially, projecting posteriorly. Internal
sac with sclerite on ventral surface as in Fig. 1/4. Spermatheca with
nodulus and ramus approximately equal in length, much shorter than
cornu.
Description.-Male, length 6.8-8.6 mm, width 2.5-3.1 mm. Female,
length 7.5-10.7 mm, width 3.0-4.5 mm. Integument medium to dark red
brown. Color and elytral pattern as in Diagnosis and Fig. 1. Pale
scales (white, tan or ochraceous) very dense, imbricate around eye,
somewhat concentrated on sides of prothorax but not forming a vitta
there, otherwise body and legs with scattered pale scales. Rostrum
1.2-1.3x longer than wide, flat or weakly concave (especially in
male), median line sharply impressed from between middle of eyes to
middie of rostrum. Dorso-lateral edges distinct but not acute,
slightly convergent caudally. Surface of head and rostrum smooth and
shiny between scales; with scattered appressed setae each set in a
puncture smaller than a scale. Epistoma as long as wide, occupying
approximately 0.3 of anterior edge of rostrum; sides of epistoma
feebly ogival, carinate anteriorly, moderately elevated, especially in
female; epistoma with an average of 3 setae on each side, usually in a
single row. Sides of rostrum with several rows of rounded scales
ventrad of scrobe; below this, scales usually replaced by appressed
white setae. Prothorax of male 1.0-1.1x wider than long, of female
1.1-1.2x wider than long; surface in both sexes with scattered fine
setae, those of disc set on smooth surface, or in a fine puncture,
Howden: Hadromeropsis ho
those of sides on smooth surface or weak tubercle. Scutellum with or
without 2 or 3 small scales and several fine appressed setae. Elytra
across humeri averaging 1.3x wider than prothorax in male, 1.5x in
female. Elytra averaging 3.1x longer than prothorax in male, 3.4x in
female. Elytra of male (Fig. 1) parallel-sided; apical umbone weak,
touching but usually not interrupting dorsal outline; apices briefly
divergent, toothed. Elytra of female with sides parallel basally,
thence gradually divergent to just behind middle where they average
1.2x wider than across humeri (1.3x in type), then abruptly
constricted under apical umbone, apex triangular between fourth
striae, ending in a pair of slightly convergent teeth. Edge of elytra
around ventrite 5 with minute setiferous tubercles in both sexes.
Disc of elytra with random glabrous spots, these as wide as an
interval and sometimes contiguous in dark areas, smaller in areas of
pale scales, larger spots convex; each spot near its caudal edge with
a seta as long as 1-2 scales, setae appressed, weakly curved or
Straight. Tubercles of intervals 8 and 9 conspicuous in dorsal view
creating a serrate outline, similar tubercles also on intervals 5, 6,
and 7 across summit of declivity; setae arising from tubercles
stouter, white, approximately as long as 2 scales, curved or straight
but parallel to surface. Female with sutural interval on declivity
with as many as 5 long, stiff setae equal in length to as many as 7
scales. Summit of declivity gradual (Fig. 14). Fore femur as in
Diagnosis; in male averaging 2.2x wider than hind femur, in female
1./x wider. Fore tibia as in Diagnosis. Ventrite 5 of male across
base 2.0x wider than long, apex broadly rounded, scales and setae
almost evenly distributed. Ventrite 5 of female across base 1./-2.1x
wider than long, apex narrowly rounded; with a few scales concentrated
on sides, scales absent or not medially; setae appressed, evenly
distributed. Male genitalia as in Diagnosis and Figs. 1/73, 174.
Female with spermatheca as in Diagnosis, Fig. 191; with a_ bursal
sclerite similar to that of argentinensis (Fig. 181) and beverlyae
(Figs. 189, 190).
Distribution. -Map 3. ARGENTINA. Misionés: Rio Parana (the type of
similis). BRAZIL. Espirito Santo: Conceigao de Barra, santa Teresa.
Minas Gerais: Matozinhos, Vigosa, Vila Monte Verde. Parana: Caviuna,
Curitiba. Rio de Janeiro: Corcovado, Itatiaya, Petropolis, Rio de
Janeiro. S40 Paulo: Bosque de Saudo, Cantareira, Interlagos,
Jabaquara, Morumbi, Parque de Estado, S40 Paulo, Sitio Banana).
Specimens were collected in all months except the winter months of
June, July, and August.
Specimens examined: 25 males, 44 females. Specimens in: Auckland,
Berlin, Cambridge, Curitiba, Dresden, Eberswalde, Leiden, London,
Maracay, New York, Oxford, Paris, Sao Paulo, Stockholm, Washington,
Howden.
Remarks.-The above Description and Diagnosis refer to the type and
specimens which are obviously conspecific with it. I have seen a
series of 12 females which I will refer to here as "smooth
nobilitatus." These specimens all differ from typical nobilitatus in
having: the elytra smooth, i.e., the glabrous areas not or scarcely
convex and the tubercles of intervals 8 and 9 weaker; caudal margin of
ventrite 4 medially acutely pointed and posteriorly directed as in
atomarius; spermatheca variable, Figs. 192, 193, 194. Instead of the
76 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
dark preapical elytral fascia, the white scales intrude on the fascia
in intervals 1, 2, and 3, and sometimes 4, reducing it to a
conspicuous dark lateral spot on intervals 4 or 5 and 6 and 7. The
scales are more pastel in color and the reflected lustre is paler.
The apical umbone is weak in all. The rostrum is as wide as long to
no more than 1.1x longer than wide. These specimens, not included in
the description, range from 7.5-9.6 mm in length and 3.0-4.0 mm in
width. They occur throughout the range of nobilitatus: Minas Gerais:
Vicosa (2); Santa Catarina (1); S80 Paulo: Jundiai (1), no other data
(5); [Argentina] Est. Esp. Loreto (1); no data (1). I have seen males
and females of typical nobilitatus with data identical to that of
smooth nobilitatus. The pointed margin of ventrite 4 always occurs in
conjunction with the smoother elytra, paler scales and different
(although variable) spermatheca. These apparently consistent
differences may indicate sibling species or two forms of females of
nobilitatus.
The relationship of atomarius to nobilitatus has some of the
attributes of a geographical cline. However, although atomarius seems
to be concentrated in the Serra do Caraga, there is some apparent
overlap in the range and without studying the situation in the field,
it seems best to leave them as separate species. The differences,
between nobilitatus and atomarius which seem to be clinal are as
follows: atomarius is smaller and has the elytral tubercles reduced,
femoral flange less developed or even absent in male, distal tibial
tooth of the male smaller, margin of ventrite 4 of female more acute,
Spermatheca more slender and elongate.
25. Hadromeropsis (Hadromeropsis) atomarius (Boheman)
Figs. 18, 19, 144, 145, 155, 175, 176, 195; Map 8
Hadromerus atomarius Boheman, 1840:292, Type, female, labelled
Typus" on red bordered with black, "H. pygalpis Germ. Brasil
Germ" written on white (Schoenherr Collection, Stockholm). See
Type Material.
Diagnosis.-Similar to nobilitatus but smaller. Metallic lustre
absent or very faint. Elytral pattern (Figs. 18, 19) similar to that
of nobilitatus but fainter, all scales white or shades of tan or
ochraceous, none obscure, rarely with faint lavender or green
reflections. Epistoma as long or longer than wide. Prothorax with
sides moderately to weakly rounded. Setiferous tubercles of intervals
8 and 9 weak in dorsal view. Fore tibia of male (Fig. 144) with
distal tooth 0.5 or less the width of tibia at apex; fore tibia of
female (Fig. 145) with two equal teeth or distal tooth slightly longer
than the second. Female ventrite 4 (Fig. 155) with caudal margin
pointed medially and slightly posteriorly directed. Male apex of
ventrite 5 slightly emarginate to truncate. Aedeagus in profile much
thicker apically than basally (Fig. 175).
Description.-Male, length 5.5-8.0 mm, width 2.0-3.0 mm. Female,
length 7.1-9.4 mm, width 2.9-3.8 mm. Integument red-brown; ventrally
piceous except ventrites 4 and 5 lighter. Color of scales and pattern
as in Diagnosis and Figs. 18, 19; scales almost evenly distributed
Howden: Hadromeropsis a
except for glabrous spots which are usually larger on basal portion of
elytra, usually 9-12 per interval. Rostrum and head similar to that
of nobilitatus in sculpture, median line and vestiture; rostrum
1.1-1.3x longer than wide in male, 1.0-1.1x longer than wide in
female. Epistoma as in Diagnosis, occupying 0.4 of anterior edge of
rostrum, triangular, anterior corners scarcely elevated. Prothorax as
in Diagnosis, male 1.0-1.1x wider than long, female 1.1-1.2x wider
than long, almost uniformly squamose, sculpture as in nobilitatus.
Scutellum with 0-8 scales. Elytra across humeri averaging 1.3x wider
than prothorax in male, 1.4x wider in female. Elytra averaging 30k
longer than prothorax in male, 3.5x longer in female. Elytra of male
with sides subparallel, sides slightly constricted beneath weak apical
umbone, apical edge of elytra very briefly indented immediately before
suture thus forming a short tooth. Elytra of female (Fig. 18) widest
at middle where they are 1.2x wider than across humeri, constricted
under weak apical umbone, apex ending in a pair of slightly convergent
teeth. Edge of elytra around ventrite 5 at most obsoletely
tuberculate. Each glabrous spot on disc with single appressed seta as .
long as 1 scale in male, longer in female; towards declivity and sides
setae longer, stouter, straight or slightly curved, less appressed,
sometimes standing well away from surface creating a shaggy effect.
Tubercles of intervals 8 and 9 weak to obsolete. Female with sutural
interval on declivity with an average of 5 long, stiff setae. Fore
femur without distal flange; fore femur of male 1.6-1.9x wider than
hind femur; of female 1.4-1.5x wider than hind femur. Fore tibia
(Fig. 144, male) bowed as in nobilitatus or less so; distal teeth as
in Diagnosis, Figs. 144, 145. Female ventrite 4 with caudal margin as
in Diagnosis, Fig. 155; male also often with a weak median point.
Ventrite 5 of male 1.4-2.0x wider than long; scales almost evenly
distributed over surface, apex as in Diagnosis. Ventrite 5 of female
1.8-2.0x wider than long; scales evenly distributed or sparser
medially, apex rounded. Aedeagus as in Fig. 175, internal sac as in
Fig. 176; spermatheca as in Fig. 195.
Type Material.-The remainder of the type series consists of: (1) a
male and a female in the Chevrolat Collection (Stockholm) labelled
"Hadromerus atomarius irroratus Klug, Brasilia," the female also
labelled "Minas Gerais" and the male "Paratypus," and (2) Var. beta
Boheman, 1840:292, a female, labelled "Typus" on red with black
border, "Brasil mer, Schupp" written on white in the Schoenherr
Collection (Stockholm). This latter specimen is teneral and has the
caudal margin of ventrite 4 somewhat less pointed than in the type but
is conspecific.
Distribution.-Map 8. BRAZIL: Minas Gerais: Matozinhos, Serra do
Caraga, Topazios (Ouro Preto).
Specimens were collected in January, February, and March.
Specimens examined: 10 males, 22 females. Specimens in Auckland,
Basel, Berlin, Cambridge, Dresden, Leiden, London, Paris, Sao Paulo,
Stockholm, Howden.
Remarks.-Boheman's statement that the body is black below would
seem to refer to speculifer, but I have no doubt that I saw the
genuine type series of atomarius.
The distally thickened aedeagus separates atomarius from both
nobilitatus and pulverulentus. In addition to the characters in the
78 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Diagnosis, atomarius differs from pulverulentus in the shorter setae
of the sides of the elytra and from speculifer in the thicker fore
femur.
Labels on museum specimens suggest the range of atomarius
apparently is concentrated in the Serra do Caraga where it 7s
sympatric with nobilitatus and pulverulentus, but field study is
needed to establish this. One female atomarius bears an identical
label to the type of pulverulentus.
See discussion of nobilitatus for further comments on the
relationship of nobilitatus and atomarius.
26. Hadromeropsis (Hadromeropsis) excubitor n. sp.
Figs. 141, 142, 177, 178, 196-198; Map 7
Diagnosis.-Similar to nobilitatus but more robust. Edge of elytra
around ventrite 5 smooth or with minute crenulations no more prominent
than the height of a convex scale. Apex of sutural interval of male
not attenuated into a tooth. Fore tibia of male (Fig. 141) with
distal tooth 0.5x or less the width of tibia; fore tibia of female
(Fig. 142) with a pair of distal teeth, the most distal tooth shorter
or equal to the second. Internal sac as in Fig. 178. Spermatheca
(Figs. 196-198) with nodulus much longer than ramus.
Description.-Holotype, male, length 10.2 mm, width 3.7 mm.
Integument red-brown. Scales arranged and elytra patterned as in
nobilitatus (Fig. 1), but markings ochraceous to copper, scales
between markings smaller, with green iridescence or Opalescence under
microscope; declivity also solid ochraceous; with reddish lustre in
glancing light. Rostrum 1.3x longer than wide. Dorso-lateral edges
of rostrum subparallel, sides of rostrum broadly visible from above;
median line vaguely impressed basally; dorsum concave; sculpture and
vestiture as in nobilitatus. Epistoma occupying 0.35 of anterior edge
of rostrum, as in nobilitatus but with 5-7 setae on each side.
Prothorax 1.1x wider than long, sides moderately rounded; sculpture
and vestiture as in nobilitatus. Scutellum with 6 small scales and
appressed setae. Elytra across humeri 1.4x wider than prothorax.
Elytra 3.0x longer than prothorax. Sides of elytra parallel to apical
third thence broadly rounded, apical umbone weak but evident in dorsal
outline; apices briefly divergent, feebly knobbed. Glabrous spots and
tubercles as in nobilitatus. Fore femur similar to that of
nobilitatus, 2.0x wider than hind femur. Fore tibia (Fig. 141) bowed
as in nobilitatus, but becoming slightly wider apicad of bend; distal
tooth 0.5x as Tong as width of tibia at apex. Ventrite 5 across base
2.4x wider than long; moderately convex apically; apex
truncate-emarginate; scales and setae slightly more numerous toward
sides. Aedeagus and internal sac of paratypes as in Diagnosis and
Figs. 177, 178 (type not dissected).
Allotype, female, length 11.3 mm, width 4.8 mm. Differs from type
as follows. Rostrum 1.2x longer than wide. Epistoma occupying 0.4 of
anterior edge of rostrum. Elytra across humeri 1.5x wider than
prothorax. Elytra 3.8x longer than prothorax. Elytra wider in
central third than in type; sides rounded-triangular beyond apical
Howden: Hadromeropsis 19
umbone, sutural interval terminating in distinct, medially directed
tooth. Sutural interval at summit of declivity with sparse line of
long, erect setae, the longest as long as 5 scales. Fore femur 2.0x
wider than hind femur. Fore tibia as in Fig. 142. Caudal surface of
ventrites 2 and 3 equal, perpendicular, evenly arcuate; margin of
ventrite 4 slightly posteriorly directed, evenly arcuate from extreme
Sides. Ventrite 5 across base 2.0x wider than long, with a slight
depression along middle of side, apex briefly truncate. Ventrite 2
evenly squamose, remaining ventrites slightly less densely squamose
medially. Spermatheca of paratypes as in Figs. 196 and 198 (allotype
not dissected).
Type Series.-Holotype, BRAZIL, Rio de Janeiro, Corcovado, GB,
X.196T M. Alvarenga, Ex-colegao M. Alvarenga (Sao Paulo). Allotype,
BRAZIL, Corcovado, Guanabara, VIII.1965, Alvarenga & Seabra, Colecao
M. Alvarenga (Curitiba). Paratypes, 12 males, 13 females. BRAZIL. 3
males, 1 female, no other data (Dresden, Oxford). Rio de Janeiro: 1
. female, no other data, Fry (London); 2 males, 1 female, same data as
- type but 1X.1961, X1.1958, VIII.1960 (S& Paulo); 3 males, 5 females,
same data as allotype but IX.1967, 3.X1.1958, X.1960, 1X.1969 [3],
18.1X.61, J. S. Moure [2] (Curitiba, Sao Paulo, Howden); 1 male,
Corcovado, GB, 6/X/967, Moure & Seabra (Howden); 1 male, GB,
Corcovado, S.A.F. Col. No. 68 (S& Paulo); 2 males, 2 females, Rio de
Janeiro, Guanabara, X.1963, 1X.1970 [2], XI1.1970, M. Alvarenga
(Washington); 1 female, Nov. Friburgo, Bescke (Oxford). No data, 2
females (Oxford, Washington).
Remarks.-Males vary in length from 8.2-10.5 mm and in width from
3.0-4.2 mm. Females vary in length from 9.4-12.8 mm and in width from
3.6-5.0 mm. The dorso-lateral edges of the rostrum range from
parallel to convergent basally. Females have as many as seven long
setae on the sutural interval on the declivity. The two teeth of the
distal end of the fore tibia of the female are equal in size in four
Specimens, unequal in the remaining nine; the distalmost tooth is
always the smaller when the teeth are unequal. In one extreme female
the second tooth is fully twice as large as the distalmost tooth.
Ventrite 5 of the female varies from 1.8-2.2x wider than long, of the
male 2.0-2.4x wider than long.
Apparently this species is concentrated on and around Corcovado,
although there is one historic Bescke specimen from Nova Friburgo (see
Papavero 1971:88). In a mixed collection the species is conspicuously
different from nobilitatus in its more robust form and reddish lustre.
The form of the distal tibial teeth in both sexes and the apex of the
elytra of the male will confirm the identification, and the genitalia
of both sexes are quite different from those of nobilitatus.
The female of atomarius also has a pair of tibial teeth, but in
that species the more distal tooth is the larger one if the two teeth
are not equal. H. atomarius differs in the weak or absent metallic
lustre, presence of a short tooth on elytral apex of male, pointed
smtp margin of ventrite 4 of female, and absent or obsolete femoral
flange.
Worn males of excubitor can be separated from the sympatric
togatus by the rostrum narrower and more concave, epistoma granular,
apical umbone less prominent, prothorax with scales of sides similar
to those of disc and not concentrated in a vitta of dense overlapping
80 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
scales, and the presence of a weak distal flange on the fore femur.
There is a sample of two males and five females from Santa
Catarina which differ from typical excubitor as follows. Males,
length 9.1-9.2 mm, width 3.4-3.5 mm; females, length 10.6-11.6 mm,
width 4.3-4.7 mm. Color subdued, lustre almost completely absent,
scales gray-green; markings faint tan or flesh colored. Scales
smaller, more numerous, the surface more completely covered, glabrous
Spots on elytra smaller, often flat, much narrower than the width of
the interval. Setae of elytral intervals more numerous, not
uniserial, randomly placed; setae straight, erect. Sutural interval
on declivity in female with as many as 12, averaging 10, long setae.
Fore femur of male 1./x wider than hind femur. The internal sac of
the male is indistinguishable from that of Corcovado specimens; the
spermatheca (Fig. 197) is very close to that of Corcovado specimens.
I am uncertain whether these Santa Catarina specimens are geographic
variants of excubitor or a sibling species.
Data on the Santa Catarina specimens are as follows: 1 male, no
other data (Berlin); 1 male, Sao Bento, 26.0S 50.0W, 800 m, Dec. 1924,
Antonio Maller (London); 1 female, Lanca, Oct. 1944, A. Maller (New
York); 4 females, Nova Teutonia, XI. 1966, XI. 1967, X.1967, X.4.1962
(Curitiba, S&o Paulo, Howden).
The position of the Corcovado range "guarding" Rio de Janeiro
Suggested the name excubitor meaning "sentinel," which at the same
time implies a relationship with nobilitatus.
27. Hadromeropsis (Hadromeropsis) fasciatus (Lucas)
Figs. 27, 146, 157, 158, 179, 180, 199, 200; Map 6
Hadromerus fasciatus Lucas, 1857:156. LECTOTYPE, HERE DESIGNATED,
female, labelled with round green disc with "11 44" in ink on
underside; vertical label "Hadromerus fasciatus, sp.n."; on green
card “Museum Paris, Rio de Castelnau" (Paris). See Type
Material.
Hadromerus herbaceus Lucas, 1857:157. LECTOTYPE, HERE DESIGNATED,
male, labelled with round green aiseowithe Pll a4 an Fak oon
underside; vertical label "Hadromerus herbaceous, sp. n."; on
green card "Museum Paris, Rio de Castelnau" (Paris). See Type
Material. NEW SYNONYMY. | roe
Diagnosis.-Moderate to large in size. Female with conspicuous
dark postmedian fascia which often appears to be composed of 3
diamonds (Figs. 27, 157), also with dark cordiform scutellar area,
this area and both edges of fascia bordered conspicuously in white.
Male tessellate with pattern similar to that of female but fainter.
Female usually with white, tan and obscure scales; male usually with
white and green or neutral scales, the latter vivid iridescent green
under microscope, less frequently with pastel blue or opalescent
scales. Sides of epistoma (Fig. 158) anteriorly slightly elevated and
produced forward in a lobe; lateral angle of anterior edge of rostrum
swollen in a distinct pterygium below scrobe and in front of antennal
insertion; these characteristics of rostrum all much more pronounced
in female than in male. Elytral declivity (Fig. 157) with conspicuous
Howden: Hadromeropsis 81
glabrous setiferous tubercles, otherwise without a naturally glabrous
spot. Edge of elytra around ventrite 5 with acute setiferous
tubercles. Internal sac without a sclerotized plate ventrally (Figs.
179, 180).
Description.-Male, length 9.2-13.6 mm, width 3.4-4.8 mm. Female,
length 10.7-16.5 mm, width 4.5-6.4 mm. Color and pattern as in
Diagnosis and Fig. 27. Densely squamose dorsally and ventrally except
ventral surface of head and rostrum and spots of prothorax and elytra
glabrous; scales often abraded from postmedian fascia of female.
Female with golden red metallic lustre (as in Lucas' description of
fasciatus) primarily on the tan and obscure scales; lustre never
strong, most frequently present on declivity; male with golden red
lustre infrequent, weaker. Scales of prothorax smaller, sparser,
often darker along median third thus creating a subvittate appearance.
Rostrum as in Diagnosis and Fig. 158. Rostrum flat or feebly concave
basally, dorso-lateral edges parallel or feebly divergent anteriorly.
Setae of head and rostrum slender, recumbent, as long as 1.5-2 scales.
Epistoma 0.25-0.3x as wide as anterior edge of rostrum. Median line
of rostrum impressed from between middle of eyes for basal half or
less, often glabrous but not impressed for remaining distance to apex
of epistoma. Prothorax 1.1x wider than long in male, almost 1.2x in
female; sides moderately rounded between constrictions; apical
constriction obsolete dorsally; female especially with vague flattened
area on disc on either side of median line. Setae of prothorax
arising from small glabrous spots, those of sides often pustulate;
setae up to 3 scale lengths. Elytra across humeri averaging 1.3x
wider than prothorax in male, 1.4x wider in female. Elytra averaging
3.0x longer than prothorax in male, 3.5x longer in female. In dorsal
view elytra of male parallel-sided from base to beyond middle thence
very gradually convergent to apical. umbone which enters outline, apex
broad beyond umbone, individual apices briefly divergent with a small
elongation or not. Elytra of female (Fig. 2/) wider at middle where
they are approximately 1.2x wider than across humeri, apical umbone
more prominent, apex approximately triangular; sutural interval at
apex produced in acute, vertically contiguous tooth. Setiferous
tubercles of intervals 8 and 9, apical umbone, and edge of elytra
around ventrite 5 acute and conspicuous in dorsal view. Elytra with
random glabrous spots ranging in size from scarcely more than the size
of a scale (in densely squamose white areas) to full width of an
interval, occasionally confluent in male especially; all glabrous
Spots convex, those of base of elytra and declivity more so, pustulate
or tuberculate. Setae arising from glabrous spots straight, often
erect on base of elytra, semi-erect on disc, erect on declivity; as
long as 1.5-5 scales, shorter in female than in male, longest on
declivity. Sutural interval on declivity with a row of 4-6 long setae
in male, 8 in female, setae longer in female than in male. Legs,
metasternum, and abdomen with many fine, long setae in male; in female
setae much sparser, shorter, curved. Fore femur 1.6-1.8x wider than
hind femur in male, 1.4x wider in female; without distal flange;
sculpture consisting of obsolete pustules at most. Fore tibia (Fig.
146) slightly bowed distally; distal tooth 0.4-0.7x width of tibia in
male, shorter in female. Male ventrite 5 across base 1.9x wider than
long, almost flat, scales slightly sparser apically only, apex
82 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
narrowly truncate. Female caudal surface of ventrites 2, 3, and 4
equal, perpendicular, polished, margin evenly arcuate; ventrite 5
across. base 1.6-1.8x wider than long, almost flat, with or without
scales. Aedeagus and internal sac as in Figs. 1/9, 180. Spermatheca
as in Figs. 199, 200; nodulus on different plane.
Type Material.-Hadromerus fasciatus Lucas, PARALECTOTYPE, HERE
DESIGNATED, 1 female, labelled like the lectotype but without the
vertical label (Paris).
Hadromerus herbaceus Lucas, PARALECTOTYPES, HERE DESIGNATED, 2
males: I male, labelled like the lectotype but without the vertical
label (Paris); 1 male, labelled with round green disc with "35-42" in
ink on underside; rectangular white label "Museum Paris, Bresil,
Parzudacki 1842" (Paris).
According to Mlle. Perrin (Mus@um National d'Histoire Naturelle,
Paris), the numbers "11 44" on the underside of the round green label
of the lectotypes of fasciatus and herbaceus represent order No. 11 of
the Castelnau collection of insects from "Rio", received at the Museum
in 1844. The "35 42" on the underside of the label of one of the
herbaceus paralectotypes refers to a collection of Coleoptera from
Brazil acquired by Mr. Parzudacki, or reaching the museum, in 1842.
Papavero (1971:149-152) describes Castelnau's trip from his
arrival in Brazil in 1843 until the insect collections ‘gathered in
and about Rio’ reached Paris. But there seems to be no way to define
the type locality, "Bresil interieur," more specifically.
Distribution.-Map 6. BRAZIL. Bahia [1]. Minas Gerais (?): Sertao
de Diamantina. Rio de Janeiro: Itatiaya, Montagnes des Orgties (Massif
de la Tijuca), Nova Friburgo, Rio de Janeiro. Santa Catarina: Corupa.
S40 Paulo.
Specimens were collected in February primarily, also March and
April.
Specimens examined: 38 males, 7/1 females. Specimens in: Auckland,
Basel, Cambridge, Curitiba, Dresden, Eberswalde, Ithaca, London,
Oxford, Paris, Sao Paulo, Stockholm, Washington, Howden.
Remarks.-Variation or extremes not included in the description
include the following. In the Diamantina male and several others, the
sides of the elytra are slightly constricted behind the humeri making
the humeri extremely prominent. This same Diamantina male has the
tubercles of the declivity especially long and acute. The vivid
metallic green iridescence common in males is almost unique to males;
only two females had any green iridescence. One female had no browns
or tan but was all gray and white without the typical female golden
red metallic lustre. In no specimens were the light and dark areas of
the prothorax sharply defined as in togatus.
The large size combined with the distinctive postmedian fascia
readily distinguish most specimens; the sharp tubercles along the edge
of the apex of the elytra are helpful in distinguishing poorly marked
specimens from togatus (no trace of tubercles), large nobilitatus
(weak tubercles) and excubitor (no tubercles). The rostral flanges
are diagnostic but not always strong; because they overhang the
mandibles they are subject to abrasion and in one specimen one of the
lobes was actually broken off.
This species frequently appeared in collections under the names
togatus, brachispinosus, and porosus (a Pandeleteius).
Howden: Hadromeropsis 83
This species grades into the subgenus Hadrorestes in_ the
tuberculate margin of the elytra and twisted spermatheca. However,
the form of the male genitalia and separated striae 9 and 10 are
clearly of the nobilitatus lineage.
Hadrorestes, new subgenus
Type-species, Hadromeropsis (Hadrorestes) pectinatus n. sp., by
present designation.
Diagnosis.-Dorsum of male glabrous or almost (except exilis);
dorsum of female glabrous to densely squamose, often within the same
species. Dorsal color pattern often formed of aggregations of scales
into specific spots, fasciae and vittae against glabrous integument.
Integument particularly thick and hard. Elytra with apical edge
around ventrite 5 conspicuously dentate or tuberculate (except in
brachypterous species). Striae 9 and 10 confluent or at least
confused under apical umbone. Male* with internal sclerites of
internal sac never flagellate; membranous parts of internal sac not
distinctly spiculate in most species, at most with very pale, minute
spicules. Apex of internal sac lightly to strongly sclerotized; apex
directed ventrally, distally, or dorsally. Female* with paired
lateral sclerites in vagina caudad of bursa copulatrix (except in
cavifrons). Spermatheca in most species with nodulus and ramus
directed in different planes.
* Male genitalia are not known for 8 of the 23 species; female
genitalia are not known for 4 species.
Description.-Scape when positioned in the scrobe exceeding the eye
in most males; in females scape exceeding eye or reaching its caudal
edge. Dorsal surface of mandible smooth, punctate, or grooved.
Dorsum and legs with or without elaborate sculpture, tubercles, and
microsculpture according to the species; sculpture always reduced in
Squamose examples of same species and sculpture of legs especially
reduced in females of same species. Elytra without rows of long,
erect setae (except institulus); many species with long, wispy setae
across base of elytra, these setae probably associated with production
of a paraffin-like wax. Middle tibia both sexes and hind tibia in
many females with a row of stout, slanting bristles.
Remarks.-With few exceptions, the species assigned to this new
subgenus On morphological characters occur at elevations of 2000 m and
above, and all are known only from the Andean cordilleras including
the Sierra Nevada de Santa Marta, but excluding the coastal cordillera
of Venezuela. <A possible exception is dialeucus described here from
seven specimens with no data except “Venezuela”.
The species seem to be uncommon; in one 10-day collecting trip in
northern Ecuador, I took five specimens representing four species. In
a trip to the Sierra Nevada de Santa Marta, H. Howden and J. Campbell
took only eight specimens of nebulicolus in a concerted effort.
The integument is so hard that the metasternum often cracks in the
pinning process, but it also probably confers some protection against
predators. In this subgenus, eight specimens (representing seven
species) had a damaged left elytron consisting of chips out of the
edge and cracks in the area of the apical umbone.
84 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
The name Hadrorestes is formed of “hadro," meaning thick, from the
first part of the generic name Hadromeropsis, and "“orestes," meaning
mountaineer, and referring to the occurrence of the sub genus in the
mountains. The name is masculine.
The alacer Group
28. alacer n. sp. 30. nebulicolus n. sp.
29. inconscriptus n. sp. 31. silaceus n. sp.
eHaracter labios of Group.-Large, 12-20 mm in Tength. Mandible
with dorsal setae set in a transverse depression which is weak or
strong, depending on the species. Eye separated by approximately its
Own diameter from anterior edge of prothorax thus forming a slight
neck (Fig. 26). Postocular vibrissae weak, consisting of a few fine,
short setae arising from a lobe or tooth. Elytra with punctures not
aligned in striae and with many extra punctures of the same size.
Elytra not flattened in profile dorsally. Multiple acute tubercles of
lateral intervals visible in dorsal outline of basal half of elytra,
weaker tubercles of declivity and edge of apex also visible in dorsal
Outline. Base of elytra with postscutellar area weakly flattened at
most; stria 5 moderately depressed. In glabrous specimens fore femur
with weak honeycomb or netted sculpture proximally; distally becoming
coarser, irregularly rugose or foveate and with weak tubercles, those
of posterior face often shelf-like in males. Fore tibia of male
slightly deflected distally; inner edge with a row of many small
denticles each rounded at its apex; outer surface of fore tibia
strigose-punctate. Fore tarsus (Figs. 302, 304, 306, 309) with
segment 2 subquadrate, abruptly tapered proximally. Female with
caudal surface of ventrites 2, 3, and 4 equal in height, smooth and
polished, the edge not acute on ventrites 2 and 3 and slightly
anteriorly directed. Internal sac internally with a_ heavily
sclerotized structure resembling a bone with condyle at proximal end;
apex of internal sac forming a short cone, the cone directed ventrally
when internal sac is evaginated.
Remarks.-Characters shared with the impressicollis group include:
elytra not striate and eye remote from anterior edge of prothorax by
its own diameter (male) or more (female). It is interesting that
these two groups and exilis, all with the eye far removed from the
prothorax, also have the postocular vibrissae greatly reduced in size.
If the postocular vibrissae are used to groom the eye, excessively
long vibrissae would be needed because of the length of the neck. It
could be argued that instead of extreme elongation to maintain the
grooming function, the vibrissae have degenerated.
In this group the apical edge of the elytra is the smoothest in
the subgenus, except for the brachypterous species.
A distinct sclerotized plate was observed inside the bursa
copulatrix of one nebulicolus and one alacer, but information on this
condition is incomplete for the group. Larger series and staining are
required for further study.
Howden: Hadromeropsis 85
28. Hadromeropsis (Hadrorestes) alacer n. sp.
Figs. 26, 201-203, 207-209, 294, 295, 302, 310, 311, 336; Map 9
Se aaa ne with lateral depression or flattened area
(Figs. , 208). Sides of metasternum and abdomen not clothed
differently from rest of metasternum and abdomen, squamose or not;
metasternum with a patch of imbricate white scales above hind coxa.
Disc of elytra in glabrous specimens (i.e., without large scales) with
foveae randomly but densely and rather evenly distributed (Fig. 203),
many contiguous and forming short transverse depressions. Apex of
elytra of female slightly triangular. Ventrite 5 of male distinctly
emarginate (Fig. 294). Ventrite 5 of female laterally not depressed
below level of margin. Apex of aedeagus simply triangular with a
slight lip.
Description.-Holotype, male, length 14.2 mm, width 5.0 mm.
Similar to Fig. 201. Black and various shades of reddish brown; head,
_ abdomen, meso- and metathorax black. Appearing glabrous
macroscopically but all surfaces except tarsi rather evenly clothed
with minute scales, those of head and rostrum ochraceous and round,
most scales elsewhere white, elongate. Ventrally with patch of dense,
white imbricate scales beside middle coxa and on posterior-lateral
corner of metasternum above hind coxa. With long, wispy setae as
follows: a few on ventral surface of apex of rostrum; on sides and
ventral surface of prothorax, on base of elytra, on remainder of
ventral surface and legs except tarsi. Head and rostrum with coarse
punctures rapidly converging to form rugae on dorsum of rostrum.
Rostrum broadly, deeply concave. Mandibular groove weak, with 2
setae. Eye especially prominent anteriorly, perpendicular to side of
rostrum. Prothorax 1.1x wider than long; sculptured as in Fig. 20/7
and Diagnosis; apical constriction weak dorsally. Elytra across
humeri 1.3x wider than prothorax, elytra 3.0x longer than prothorax.
Sculpture of elytra as in Diagnosis and Fig. 203. Setae of disc of
elytra inconspicuous, approximately as long as the diameter of one
fovea; setae of lateral intervals similar to those of silaceus but
Shorter. Apex of elytra as in Fig. 202, briefly truncate. Summit of
declivity with 9 long setae on sutural interval, these long setae
approximately as long as the setae on apical margin of elytra, much
Shorter than the long setae on summit of declivity in female. Fore
femur similar to but more strongly sculptured than Fig. 109; 2.2x
wider than hind femur; inner edge with strong, brief, arcuate flange;
posterior face with 10 very strong and several weaker shelf-like
tubercles. Fore tibia with a few granules on inner surface; outer
surface of all tibiae very strongly sculptured. Fore tarsus as in
Fig. 302. Ventrite 5 as in Diagnosis and Fig. 294; 2.0x wider than
long. Last tergite with fine microsculpture between small punctures.
Aedeagus and internal sac as in Figs. 310, 311.
Allotype, female, length 16.5 mm, width 6.7 mm. Differing from
type as follows. Similar to Fig. 26. Integument reddish except
black head, meso- and metathorax, ventrites 1 and 2 and median vitta
On pronotum. Squamose except as follows: scales abraded from more
elevated positions as dorso-lateral edges of rostrum, median line of
pronotum, elytral suture, and transverse arc on metasternum, the black
86 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
or reddish color of the integument thus forming dark markings. With
round ochraceous scales dorsally and ventrally and on legs; scales
more elongate on sides and ventral surface of head and rostrum, very
densely imbricate near middie and hind coxa where male has white
Spots; scales greenish white on pronotum and on disc of elytra in 3
obscure fasciae; scales darker and abraded in broad fascia at apical
third. Sculpture of head, rostrum and pronotum absent, replaced by
scales. Rostrum with shallow concavity, median line deeply foveate
between eyes. Prothorax with apical constriction unmarked on disc,
with tubercles of sides replaced by shiny granules scarcely larger
than a scale. Elytra across humeri 1.5x wider than prothorax, elytra
3.4x longer than prothorax. Sculpture of elytra reduced, the larger
concentrations of scales in depressed areas. Apex of elytra slightly
triangular, ending in a brief tooth, with slight swelling at junction
of intervals 3 and 9. Sutural interval with approximately 10 long
setae at summit of declivity (some obviously broken off). Fore femur
1.2x wider than hind femur. Ventrite 5 (Fig. 295) weakly convex
longitudinally, laterally flattened, 1.75x wider than long. Genitalia
Of paratypes as in Fig. 336; spermatheca very slightly deflected
between nodulus and ramus; spermathecal duct 3-4 mm long, attached to
a faint sclerite within bursa copulatrix.
Type Series.-Holotype, COLOMBIA, Staudinger (Dresden). Allotype,
COLOMBIA; Bogota, Fry Coll. 1905-100 (London). Paratypes, 3 males, 4
females. COLOMBIA. Valle: 1 male, 1 female, Caucathal, Coll. J.
Faust, Ankauf 1900 [1], Gehr W. Muller Vermacht 1909 [1] (Dresden).
ECUADOR. Carchi-Napo border: 1 female, Sebundoi, 11-15.1X.1977, 2600
m, L. Pefia (Howden). Napo: 2 males, 7 km S Baeza, 2000 m, 21,
25.11.1979, H & A Howden, on bamboo [1] (Howden). Pichincha: 1 female,
Quito, 24362, Fry Coll. 1905-100 (London). Tungurahua: 1 female,
Runtun, 22.X1.1938, Coll. F.M.Brown (New York).
Remarks.-The males vary in length from 12.4-14.0 mm and in width
from 4.1-4.8 mm. Females vary in length from 14.0-17.6 mm and in
width from 6.1-7.0 mm. The male paratype from Colombia has coloring
as the type, and the two from Ecuador are all black except the femora
reddish. The type has many more scales on: the head than the other
males. Two males lack the middle coxal spot, all have the hind coxal
spot. The apex of the elytra in all males is less truncate than in
the type. The internal sac was dissected in three of the four males;
two females were dissected, one each from Colombia and Ecuador.
The two males from Baeza are so different in habitus that special
mention is made of them here. Figures 208 and 209 illustrate their
much smoother integument. In addition they are smaller, have fewer
long wispy setae, and lack the long setae at the summit of the
declivity.
The female from Colombia is not squamose as the allotype, but
covered with minute scales as the holotype; the sculpture on this
Specimen is slightly reduced from that of the holotype. All] squamose
females (Fig. 26) have the median line of the pronotum dark, a dark
area bordering the postscutellar depression, and a short to wide
fascia at the apical third, the latter widest in the allotype in which
it extends the full width of the elytra.
Many specimens have the dorso-lateral edge of the elytra (interval
8 of striate species) from the humerus to the apical umbone slightly
Howden: Hadromeropsis 87
elevated.
It is the sculpture of the elytra and form of the prothorax that
help to associate the sexes of silaceus and alacer when dealing with
Squamose females and glabrous males. Also, in silaceus both sexes
seem to lack the erect long setae on the sutural interval whereas they
are present, often in both sexes in alacer.
Of the specimens from Baeza, one was collected when it flew onto a
bamboo overhanging the path and the other was taken on an unidentified
herbaceous plant nearby. Both specimens were very lively, hence the
name alacer.
29. Hadromeropsis (Hadrorestes) inconscriptus n. sp.
Faqs. 204.) 298.):299 7304 24312.9839: Mapped
Diagnosis.-Similar to alacer but setae of disc of elytra (Fig.
204) as long as twice the diameter of a fovea; fore femur of male with
entire distal half almost uniformly set with small shelf-like
tubercles; cone-like apex of internal sac longer (Fig. 312);
spermatheca very long and twisted (Fig. 339).
Description.-Holotype, male, length 14.2 mm, width 5.0 mm. Black,
Shading to piceous at extremities. With minute oval or elongate
elliptical white scales on head, rostrum, sides of prothorax, elytra;
scales very sparse ventrally. With patch of imbricate white scales on
metathorax in front of hind coxa and a few scales clustered on side of
ventrites 3 and 4. With long, wispy setae as follows: on sides and
apex of ventral surface of rostrum, on prosternum (none on sides), a
few across base of elytra, on remainder of ventral surface and legs
except tarsi. Head and rostrum strongly punctate, very few punctures
confluent along median line, otherwise similar to alacer. Prothorax
1.1x wider than long, lateral depressions more conspicuous than in
alacer; median line convex and punctate, sculpture rapidly changing to
discrete tubercles each bearing a long, curved seta; apical
constriction weak dorsally. Elytra across humeri 1.2x wider’ than
prothorax, elytra 2.5x longer than prothorax. Base of elytra without
postscutellar depression. Elytral sculpture as in Fig. 204, foveae
very deep and crowded, rarely confluent. Setae of elytra as in
Diagnosis; setae of lateral intervals only slightly longer than those
of disc; sutural interval at summit of declivity with setae much
longer. Apices of elytra briefly, individually rounded. Fore femur
2.2x wider than hind femur; inner edge with strong, brief, arcuate
flange. All setae of femora and tibiae long and wispy. Fore tarsus
as in Fig. 304. Ventrite 5 in Fig. 298. Last tergite sculptured as
in alacer but setae much more numerous and longer. Aedeagus similar
to that of alacer; internal sac as in Fig. 312 and Diagnosis.
Allotype, female, length 15.3 mm, width 6.2 mm. Differs from
holotype as follows. Scales more numerous; with a very small cluster
of scales beside middle coxa. Long, wispy setae reduced in number
except on abdomen. Sculpture of head and rostrum weaker, concavity
elongate triangular from about middle to very deep fovea on median
line between eyes. Prothorax with sculpture weaker. Elytra across
humeri 1.4x wider than prothorax, elytra 3.3x longer than prothorax.
88 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Elytra widest at middle, sides gradually rounded from there to apex,
umbone very weak, just touching dorsal outline; apex with short tooth.
Elytra with foveae more frequently confluent. Sutural intervals at
summit of declivity with approximately 8 long setae. Fore femur 1.4x
wider than hind femur. Ventrite 5 (Fig. 299) across base 1.7x wider
than long, evenly convex from base to narrow apex, sides not at all
flattened, surface coarsely but sparsely punctate, with very long
setae. Spermatheca as in Fig. 339 and Diagnosis; spermathecal duct
2.5 mm long.
Type Series.-Holotype and allotype, PERU, Cuzco, Alfamayo, 40 km
SE Nad labanbe, Elev. 2600 m, 8.Jan.1979, W.E. Steiner, mating pair
(Washington, USNM Type No. 100194).
The pair was taken on new growth on a woody composite.
Remarks.-Until it was cleaned with ammonia, the male had every
elytral fovea filled with wax and all the long, wispy setae matted
down with the semi-opaque wax.
The characteristics of the male and female genitalia were the
prime reason for considering this a different species from alacer. As
additional specimens become available, the other differences noted
can be assessed for variation and possible diagnostic’ value:
individually rounded apices of elytra in male, weaker apical umbone,
slightly less prominent eye, and presence of scales on ventrites 3 and
4. In addition, the locality may be significant.
A female from Yungas de La Paz (Kuschel Coll., Auckland) may be
this species. The specimen is 12.7 mm long, 5.0 mm wide and differs
from the allotype as follows: prothorax rather strongly sculptured;
elytral tooth obsolete; sutural interval at summit of declivity with
only 3 long setae; abdomen densely squamose except for flat circular
glabrous spots from which setae arise; scales more elongate centrally
on abdomen; surface of ventrite 5 with sides flat, punctuation weaker;
Spermathecal duct 4.0 mm long. The specimen is missing both fore
legs. The spermatheca and lateral sclerites are as in Fig. 339.
Hadromeropsis impressicollis males bear a superficial resemblance
to alacer and inconscriptus especially in the prothorax and coxal
spots, but impressicollis differs in the base of the elytra not
impressed at stria 5, elytral foveae much more distant, rostrum more
nearly perpendicularly sided, scutellum white-scaled, and other group
Characteristics. Note in Fig. 312 the proximal end of the internal
sclerite is split and elongated dorsally, in this respect being
intermediate between impressicollis and the other alacer group
Species. :
The name "“inconscriptus" means "“unarranged" and refers to the
appearance of the elytral punctures.
non
30. Hadromeropsis (Hadrorestes) nebulicolus n. sp.
Figs. 205, 296, 306, 313, 314, 338; Map 9
Diagnosis.-Elytra sparsely (in male) or densely (in female)
clothed with rounded white and pale colored scales, both sexes with a
Vague postmedian V or U-shaped fascia outlined in larger, usually
paler scales; some specimens with metallic green scales ventrally and
Howden: Hadromeropsis 89
on sides of elytra. Female with, male without long, erect setae at
summit of declivity. Elytral striae often faintly discernible.
Ventrally with an area of imbricate scales on metasternum above hind
coxa, often with other patches as well. Last tergite of male very
finely, sparsely, punctate; setae short. Cone-shaped apex of internal
Sac evenly sclerotized (Fig. 313).
Description.-Holotype, male, length 14.6 mm, width 5.0 mm. Black,
extremities shading to piceous. Patterned dorsally with scales of
various sizes from small to medium, mostly rounded, white and pale
shades of gray, ventrally some vivid blue-green as well. Scales of
head and rostrum very sparse, not arranged in a pattern except a
partial border above eye; scales of pronotum slightly more numerous
and larger in a vague vitta between eye and stria 4; scales of elytra
with larger white scales vaguely defining a basal semicircle and a
postmedian "V". Ventrally with blue-green scales in a small patch on
fore coxa and beside it, on mesepisternum anteriorly, on side of
middle coxa, on metepisternum (very small cluster), on metasternum
laterally adjacent to hind coxa and continuing onto coxa itself, and
in small clusters on side of every ventrite. With long, wispy setae
as in alacer. Head and rostrum densely, finely punctured; some
punctures confluent in concavity. Mandibular groove weak but
distinct. Eye moderately prominent anteriorly. Prothorax almost as
long as wide, sides widest caudad of middle, lateral flattened area
obsolete. Pronotum with median line very finely, partially impressed,
Otherwise sculpture of disc similar to that of alacer. Elytra across
humeri 1.3x wider than prothorax, elytra 2.8x longer than prothorax.
Elytral sculpture with fewer extra-strial punctures or foveae than in
alacer, striae partly discernible amongst the other’ sculptural
details; with various irregular, rectangular, depressed areas
containing aggregations of scales. Setae of elytra compared to those
of alacer slightly longer, more conspicuous, white; setae of sutural
interval at summit of declivity scarcely longer, less curved; setae of
lateral intervals as in alacer. Apices of elytra very slightly
individually rounded. Fore femur 1.7x wider than hind femur;
posterior face with about 10 weak shelf-like tubercles; distal flange
weak, with several small tubercles on edge. Sculpture of tibia weaker
than in alacer. Fore tarsus as in Fig. 306. Ventrite 5 (Fig. 296)
broadly truncate-emarginate. Last tergite as in Diagnosis. Aedeagus
as in Fig. 314; internal sac not evaginated in type, in paratypes as
in Fig. 313 and Diagnosis.
Allotype, female, length 17.8 mm, width 7.1 mm. Differs from type
as follows. Densely covered dorsally and ventrally with ochraceous
scales; integument naturally glabrous only briefly along median line
Of pronotum and broadly medially on metasternum and abdomen where
scales are distant. Scales particularly dense ventrally where type
has patches of scales. Pattern of elytra similar to that of type but
encircled areas filled with darker scales; interval 9 from base to
middie and interval 8 from middle to apex paler, forming an indistinct
Vitta. Sculpture of head, rostrum and prothorax replaced by scales;
rostrum only weakly concave, median fovea between eyes extremely deep.
Prothorax 1.2x wider than long. Elytra across humeri 1.5x wider than
prothorax, elytra 3.6x longer than prothorax. Disc of elytra (Fig.
205) almost smooth, weakly undulating between very faintly impressed
90 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Striae; glabrous areas of postscutellar region subtuberulate. Sutural
interval at summit of declivity with 5 very long setae and 5 or more
slightly shorter ones. Apex of elytra scarcely constricted under
apical umbone, gradually and slightly rounded to short tooth. Fore
femur 1.1x wider than hind femur. Ventrite 5 feebly convex apically,
apex narrowly truncate, 2x wider than long. Genitalia of paratypes
(two dissected) as in Figs. 338; spermatheca in one plane;
Spermathecal duct 2.5-3.0 mm long, attached to a large vertical
sclerotized plate at caudal end of the bursa copulatrix. Lateral
sclerites connected caudally by a large U-shaped sclerotization in
one.
Type Series.-Holotype, COLOMBIA, Magdalena, San Lorenzo, 41 km §
Sta. Marta, 7/000 ft, V.5.1973, Howden and Campbell (Howden).
Allotype, same data as type but V.9.1973 (Howden). Paratypes, 3
males, 3 females. COLOMBIA. Magdalena: 1 male, 2 females, same data as
type but V.3.1973 [1 female], V.7.1973 [1 female], V.9.1973 [1 male];
males, 1 female, San Lorenzo Area, 44 km S Sta. Marta, 8000 ft,
V.11.1973, Howden and Campbell. Paratypes in Ottawa, Washington,
Howden.
Remarks.-Males vary in length from 11.8-15.0 mm and in width from
3.9-5.3 mm. Females vary in length from 17.8-19.0 mm and in width
from 6./-6.8 mm. The most striking variation is in the coloring of
the females; one is similar to the allotype, but the other two are
iridescent-scintillating green on all ventral surfaces and legs, sides
Of head and rostrum, most of prothorax and base of elytra; in one
specimen the postmedian fascia is green also. In one male there are a
few large scales scattered along the metepisternum. In two of the
males the shelf-like tubercles of the fore femur are weaker than in
the type; in the third male they are stronger than in the type.
The left elytron of the type has a nip out of the margin and both
hind tibiae nicked as if by predators. One of the females has a
Similar nip and a parallel nip on the opposite elytron with the edge
cracked, as well as a longitudinal crack on stria 5 near the base.
In the other three species in this group the apical fascia (when
present) is transverse; in nebulicolus it is always distinctly V- or
U-shaped.
The species is endemic to the Sierra Nevada de Santa Marta where
it was taken in the cloud forest, hence the name nebulicolus, meaning
“living in the clouds". The collecting site is described and
illustrated by the collectors in Howden and Campbell (1974).
31. Hadromeropsis (Hadrorestes) silaceus n. sp.
Figs. 206, 297, 309, 315, 316, 337; Map 9
Diagnosis.-Glabrous specimens with a vitta on lateral edge of
metasternum formed by dense, imbricate, oval white scales; vitta
continuing down sides of abdomen almost to apex and anteriorly present
On mesepimeron. Pronotum without lateral depression. Disc of elytra
of male (Fig. 206) with strial punctures small, surrounding surface
smooth or minutely sculptured. Apex of elytra of male and female
broadly rounded. Ventrite 5 of male broadly truncate-emarginate (Fig.
Howden: Hadromeropsis 91
297), 1.9-2.2x wider than long. Ventrite 5 of female laterally
phe Eee ented level of side margin. Apex of aedeagus very elongate
Pao SPS)
Description.-Holotype, male, length 18.7 mm, width 6.3 mm. Black
to piceous. orsally without scales except a few minute ones on apex
of elytra; small, rounded scales on legs; imbricate oval scales
ventrally as in Diagnosis; all scales white. With conspicuous,
numerous, long, wispy setae on sides and ventral surface of rostrum;
on prothorax dorsally on basal constriction, on sides and on ventral
Surface; on elytra across base; on entire ventral surface, but sparse
on abdomen and on all legs. Head and rostrum irregularly punctate;
rostrum moderately longitudinally concave; apex of rostrum and
mandibles with many extra, long setae. Mandible foveate-punctate,
dorsal 5 or 6 setae contained in foveae in a broad, sharply marked
transverse depression. Prothorax 1.1x wider than long; disc slightly
evenly convex, basal and apical constrictions equal on sides, apical
constriction unmarked on disc, median line unmarked in any way. Disc
Of pronotum smooth, only very finely, sparsely punctate; sides of
prothorax with moderate, discrete tubercles, the long setae arising
from punctures as well as from tubercles. Elytra across humeri 1.4x
wider than prothorax, elytra 3.2x longer than prothorax. Elytra
sculptured as in Fig. 206 and Diagnosis. Setae of lateral intervals,
declivity, and edge of elytra short, fine, curved, numerous, 2 or more
rows per interval. Apex broadly rounded with brief emargination
before suture. Fore femur 1.8x wider than hind femur, distally with a
moderate flange with crenulate edge; posterior face with 12 or more
weak shelf-like tubercles. Inner surface of fore tibia with several
granules. Fore tarsus as in Fig. 309. Ventrite 5 as in Fig. 297 and
Diagnosis. Last tergite shiny between large punctures. Aedeagus and
internal sac as in Figs. 315, 316.
Allotype, female, length 18.4 mm, width 7.5 mm. Differs from type
as follows. All surfaces dorsally and ventrally including legs
(except tarsi) evenly covered with small, round, convex, ochraceous
scales; scales mostly contiguous except at follicles and granules.
Elytra also with pale pinkish scales forming an obscure pattern of a
pair of basal rings and various zigzag fasciae. Erect setae
apparently as numerous as in type but shorter, those of sides of
prothorax especially conspicuous, perpendicular to surface. All
sculpture less evident, mostly replaced by scales. White scales of
ventral surface of male replaced by densely imbricate ochraceous
scales. Prothorax 1.2x wider than long; tubercles of sides replaced
by shiny granules averaging diameter of 1 scale. Elytra across humeri
1.5x wider than prothorax, elytra 3.6x longer than prothorax.
Postscutellar depression concave. Sides of elytra slightly (1.1x)
wider at middle, apex similar to that of male. In profile elytra
evenly convex from about basal third, summit of declivity scarcely
perceptible; setae of sutural interval on declivity of uniform length,
not longer at summit of declivity. Fore femur 1.1x wider than hind
femur. Ventrite 5 as in Diagnosis, 2x wider than long. Genitalia of
paratype as in Fig. 337; spermathecal duct 2.5 mm long; spermatheca in
one plane.
Type Series.-Holotype, COLOMBIA, Baden, coll. J. Faust, Ankauf
1900, siaarONe ds hirtipes J Faust" (Dresden). Allotype, COLOMBIA,
92 Contrib. ‘Amer. Ent. Insta,’ vole 29) no. 6, 1982
same data as type except "“Hadromerus silaceus J. Faust" (Dresden).
Paratypes, 4 males, 2 females. COLOMBIA. [Antioquia?] : 1 female,
Frontina (Oxford). Valle: 1 female, Cauca, ex coll Clerc (Paris). No
data, 2 males (Oxford, Howden). Questionable data, 2 males,
"Brasilien," Coll. C. Felsche, Kauf, 20, 1918 (Dresden).
Remarks.-Males vary in length from 14.6-17.0 mm and in width from
5.0-6.1 mm; one female is 20.5 mm in length, 7.0 mm in width. The
female from Cauca is mostly glabrous, with the elytra sharply
patterned with dense, overlapping, small, round scales forming a basal
ring, median zigzag fascia, and reverse zigzag fascia across apical
third, the latter fascia on side continuing along interval 8 beneath
apical umbone in an oblique line to suture; punctures in the naturally
glabrous areas slightly larger than in Fig. 206. The paratypes
Otherwise vary little from the type. The semi-opaque paraffin-like
wax is common on the males. None of the females has the long setae
commonly found on the summit of the declivity in females.
The species is readily distinguished by the diagnostic characters
listed.
Faust's manuscript name, "hirtipes", would be very apt for the
Species, but the stem has been used often in Tanymecini, so I have
chosen the name he attached to the female, "silaceus," which aptly
describes the ochraceous color of the squamose females.
The exilis Group
32. exilis n. sp.
Characteristics of Group.-Head somewhat elongate, eye separated by
Q./x its own diameter from anterior edge of prothorax. Postocular
vibrissae weak. Fore femur slender, without sculpture. Internal sac
with spiculate lobes; sclerotized apex long, straight, distally
directed.
Remarks.-H. exilis is intermediate between the alacer and
impressicollis groups in the characters above. The species, and hence
the group, 1s represented by a single rather abraded male and it is
therefore difficult to assess the characters of punctuation, setae,
etc.
32. Hadromeropsis (Hadrorestes) exilis n. sp.
Figs. 363-366
Diagnosis.-Based on unique male. Slender, elytra elongate oval.
Clothed with round, iridescent green scales. Brachypterous: wing 0.7x
length of elytron, mesepimeron narrow, elytra narrow across humeri.
Edge of elytra smooth. Fore femur very slender.
Description.-Holotype, male, length 10.1 mm, width 3.8 mm.
Integument black, legs and antennae reddish. Dorsally apparently
Lspecimen abraded] evenly, sparsely clothed with round, iridescent
green scales the same size as those of gemmifer. Ventrally scales
concentrated on sides, only occasional scales in central third.
Apparently without long, wispy setae. Head and rostrum (Figs. 363,
Howden: Hadromeropsis 93
364) robust, rostrum approximately as long as wide. Dorso-lateral
edges well marked on distal half, gradually weakening and convergent
basad. Dorsum of rostrum gently sloped towards median line, median
line deeply impressed between anterior half of eyes only. Lateral
angle of anterior edge of rostrum slightly produced, extending beyond
apex of scrobe more than usual in the genus. Epistoma approximately
1.5x longer than wide, apical edge deeply excised (worn?) (Fig. 363);
epistoma occupying 0.26 of anterior edge of rostrum. Surface of head
and rostrum smooth except for shallow punctures, some punctures
contiguous on base of rostrum. Mandibles positioned so that their
dorsal surface not visible. Eye large, round, strongly convex.
Prothorax 1.05x wider than long, sides slightly rounded between equal
basal and apical constrictions, basal constriction continuous across
disc of pronotum, apical constriction absent on disc.. Pronotum (Fig.
364) without depressions, weakly convex; sculpture consisting of
minute punctures medially, obsolete tubercles laterally. Elytra
across humeri 1.3x wider than prothorax, elytra 3.0x longer than
-prothorax. Elytra as in Diagnosis, summit of declivity and apical
umbone unmarked. Elytral striae with distinct, slightly irregularly
Spaced punctures, some glabrous areas indistinctly elevated on
intervals, otherwise with no sculpture. Edge of elytra smooth,
without any trace of denticles or tubercles. Apices of elytra briefly
divergent, produced in a short, blunt tooth. Setae abraded, but
intervals 8 and 9 with prostrate white setae as long as 2 scales.
All legs long, slender, with scattered minute punctures, otherwise
without sculpture; fore femur 1.3x wider than hind femur, without
distal flange; fore tibia almost straight, with 8 small teeth on inner
edge, distal tooth only slightly larger, concealed in setae. Middle
coxae more protuberant than usual for genus, mesepisternum
consequently convex. Prosternum and metasternum finely striguiate.
Abdomen long and narrow; ventrite 5 across base 1.4x wider than long,
slightly, evenly convex, surface smooth and: polished with sparse fine
punctures; apex truncate. Genitalia as in Figs. 365, 366; apex of
aedeagus cupped and minutely spiculate.
Type Series.-Holotype, male, BOLIVIA, Chapare, 400 m, 3.1951,
seuelba leg., Coll. Kuschel (Auckland).
Remarks.-H. exilis is rich in characters as discussed in the group
Remarks and species Diagnosis.
It is surprising to find this flightless species at such a low
altitude as 400 m. Of the other flightless Hadromeropsis, one occurs
at a high altitude of 3/60 m in Colombia and the other has no data.
The word exilis means thin, weak, and refers to the slender
habitus and inbility of this species to fly.
The impressicollis Group
33. impressicollis (Kirsch) 35. bombycinus n. sp.
34. institulus n. sp. 36. brachypterus n. sp.
Characteristics of Group.-All scales greatly elongate (Figs. 213,
215, 219). Both sexes with scutellum very densely clothed with very
long, imbricate white scales; with small patches of similar scales on
anterior face of fore femur proximally, on mesosternum beside coxa,
94 ContriDs Amer: Ent. olnst:, vole 19, no; 6, 1982
and on metasternum anterior to hind coxa. With long, wispy setae on
base of elytra except in brachypterus. Pronotum with a pair of
lateral depressed or flattened areas as well as median line depressed
(Figs. 212, 213, 219) except in brachypterus (Fig. 227). Setae on
tubercles of intervals 8, 9, an not strongly curved or erect,
prostrate or nearly so. Posterior face of fore femur of male (known
only for impressicollis) with shelf-like tubercles. Anterior face
and/or outer edge of all tibiae of both sexes covered with conspicuous
crowded grooves or strigae.
Remarks.-Three of the four species in this group are represented
by females only, and the female genitalia could not be studied for the
only species represented by both sexes. H. impressicollis males share
the peculiar shelf-like tubercles of the posterior face of the fore
femur with the alacer and pectinatus groups.
In the characteristics of the male genitalia and long neck, this
group is intermediate between the alacer and exilis groups on the one
hand and the remaining Hadrorestes on the other. In impressicollis
the apex of the internal sac (Fig. 317) is almost straight, only very
slightly curved ventrad, thus beginning the transition from a
ventrally directed to a dorsally directed apex; in this respect the
distally directed apex of exilis is more advanced. The proximal end
of the internal sclerite has a small dorsal spur, transitional between
the condyle-shaped end and the strongly reflexed form of the remainder
of Hadrorestes.
33. Hadromeropsis (Hadrorestes) impressicollis (Kirsch)
Figs. 210-214, 303, 317-319; Map 11
Hadromerus impressicollis Kirsch, 1867:233. Type, unique male,
abelled ‘Bogota, Kirsch" in India ink on green paper (Dresden).
Hadromerus ruficrus Kirsch, 1867:232. Type, unique female, labelled
Bogota, Kirsch" in India ink on green paper (Dresden). NEW
SYNONYMY.
Hadromeropsis subaeneus Voss, 1953:61. Type, destroyed (Striimpel, in
att.) Paratype, female, labelled "Socorro Col. 3500"
handwritten, "Sig. C. Rudel, Eing. Nr. 1/49" mechanically
printed, "Hadromeropsis subaeneus m." handprinted on white,
"Paratype" mechanically printed on orange, "Coll. E. Voss, Eing.
3-75" mechanically printed on white (Hamburg). NEW SYNONYMY.
Diagnosis.-Rostrum with conspicuous longitudinal parallel rugae
from interantennal line to head behind eyes, each groove infrequently
interrupted and curving around the elongate frontal pit (Fig. 210).
Prothorax (Figs. 212, 213) tuberculate, more strongly so on sides and
elevated areas, the depressed areas of pronotum and space between
tubercles may be smooth and shiny, or transversely rugulose, or
minutely granulate; any scales present extremely long and narrow (Fig.
213 hy
ek ell hse length 11.0-13.0 mm, width 4.0-4.8 mm. Female,
length 14.0-15.0 mm, width 5.6-6.1 mm. Black; antennae, legs and apex
of rostrum reddish becoming piceous in older specimens, sometimes with
subaeneous lustre in depressed areas of prothorax where glabrous.
Howden: Hadromeropsis 95
Scales white or off-white. Maximum vestiture of females: short,
sparsely set scales on head and rostrum as in Fig. 210; side of head
with denser, longer scales; prothorax on side (Fig. 213) with very
densely placed, very long scales giving a shaggy, furry appearance,
these scales sparser in lateral depressions and replaced medially by
sparse, shorter scales directed anteriorly; elytra with long scales
moderately closely placed except for glabrous trifasciate pattern of
indistinct arc at base, oblique fascia before middle, and parallel
oblique fascia halfway to apex. Minimum vestiture of female:
prothorax with scales absent on disc, reduced to vitta on side; elytra
with only a few scales medially, remainder of surface with minute
scales like the setae of strial punctures. Vestiture of male like
minimum vestiture of female. Long, wispy setae present on ventral
surface including ventral surface of femora and tibiae, on base of
elytra, and, at least in female, on sides of prothorax. Rostrum as in
Diagnosis and Fig. 210. Eye separated from anterior edge of prothorax
by its own diameter. Prothorax 1.1-1.3x wider than long in male,
~1.25-1.3x wider in female. Prothorax as in Diagnosis and Figs. 212,
213; when glabrous, sculpture much more evident; median depression
weaker in female, absent in subaeneus paratype. Elytra across humeri
1.2x wider than prothorax in male, 1.3x wider in female; elytra
2.8-3.0x longer than prothorax in male, 3.3-3.6x longer in female.
Apical umbone scarcely distinguishable. Apices of elytra briefly
individually rounded in male; in female with a very brief tooth (Fig.
214). Sutural interval at summit of declivity without additional long
setae in male; in female with at least 1 very long straight and
several long curved setae. Elytral intervals except on disc with a
row of tubercles, each tubercle approximately the diameter of a strial
puncture, female in addition with a few weak transverse rugosities,
intervals 7 and 8 "with less regular rows of tubercles, so that the
side contour of the elytra appears crenulate’ as in the description of
Subaeneus by Voss (1953:62). Each tubercle with a single fine seta,
those of extreme base long, erect and wispy, those elsewhere curved;
setae present the length of each interval whether arising from
tubercle or not. Strial punctures ranging from nowhere aligned to
perfectly aligned in rows (1 male); on declivity striae confused to
absent in all specimens. Fore femur of male 1.8-2.0x wider than hind
femur; inner edge with abrupt conspicuous, short, thick flange, its
edge crenulate or smooth; anterior face of fore femur rugulose on
distal half; posterior face with shelf-like setiferous tubercles
moderately to strongly developed. Fore femur of female 1.3-1.4x wider
than hind femur; posterior face without shelf-like tubercles. Fore
tibia on inner edge with 8-18 nearly uniform equidistant teeth,
proximally with a slight flange opposite the femoral flange. Fore
tarsus of male as in Fig. 303. Metasternum granulate or tuberculate,
the sculpture much weaker in female. Ventrite 5 of male 2.0x wider at
base than long, apex broadly truncate; surface flat, punctate, the
punctures much denser apically. Male genitalia as in Figs. 31/-319.
Ventrite 5 of female (Fig. 211) 1.8x wider at base than long. Female
genitalia unknown - see Remarks.
Distribution.-Map 11. COLOMBIA. Cundinamarca: 1 male, 1 female,
Bogota, Kirsch (the types of ruficrus and impressicollis) (Dresden).
Valle: 1 female, Socorro, 3500 m (the paratype of subaeneus)
96 Contrib. Amer. Ent:°Inst., vol.°19, no. 6, 1982
(Hamburg). No additional locality: 1 male, Felipe Ovale, Q. Ac. 33501
(New York); 1 male, Pascoe Coll. 93-60 (London); 1 female, Muro
(Paris); 1 male (Pittsburgh).
Remarks.-The abundant variation observed in the short series is
incorporated in the description. Some scales have an iridescent green
reflection in certain lights in the densely squamose female.
The female genitalia are unknown. Of the three females seen, two
are types and were not dissected. The third specimen had apparently
been crushed while alive and the entire contents of the abdomen exuded
and removed; when the specimen was dissected the abdomen was empty.
Both the names ruficrus and impressicollis are equally descriptive
and appropriate for the species, but neither is uniquely distinctive.
Although ruficrus has page priority, the name impressicollis is chosen
for this species since it is more distinctive among the names already
in the genus.
The high, cold Monte Socorro site is described in Fass]
(1915:57-58).
34. Hadromeropsis (Hadrorestes) institulus n. sp.
Figs. 29, 215-218, 340; Map 11
Diagnosis.-Based on female only. Similar to impressicollis female
but pattern of elytra tessellate, not at all fasciate; elytra strongly
constricted beneath apical umbone; apex of elytra conspicuously flared
outward (Figs. 29, 215, 218); and ventrite 5 narrow basally.
Description.-Holotype, female, length 12.2 mm, width 5.0 mm.
Black; antennae, legs and rostrum reddish; elytra with faint
sSubaeneous lustre. With patches of long, imbricate, white scales
ventrally and on scutellum as in group, but all other scales
ochraceous. Scales of head and rostrum as in Fig. 216, evenly
distributed on sides. Sides of prothorax with very long scales in a
dense vitta; scales of disc of prothorax as in Fig. 217. Elytra with
dense patches of very long scales irregularly alternating with
glabrous areas of approximately the same size; scales in vicinity of
scutellum, humeral angles and apical umbone half the size of the other
scales (Fig. 215). Rostrum as in Fig. 216, but weakly concave. Eye
separated from prothorax by approximately its own diameter. Prothorax
(Fig. 217) scarcely 1.2x wider than long; disc flattened on sides,
depressed along median line; in dorsal view long, wispy setae arising
from lateral and ventral surfaces particularly conspicuous. Elytra
(Fig. 29) across humeri 1.4x wider than prothorax; elytra 3.4x longer
than prothorax. Sides of elytra gradually divergent to about apical
third where they are 1.3x wider than across humeri, thence broadly
rounded, strongly constricted under very prominent apical umbone,
expanded apex thus forming a very conspicuous flounce (Figs. 215,
218). With long, wispy setae on at least apical third of intervals
1-4, a few on interval 5; sutural interval with 8-10 long, wispy setae
distributed down center of interval, not concentrated on edge of
interval at summit of declivity. Elytral tubercles as described for
impressicollis female. Strial punctures in slightly irregular rows,
disappearing before declivity. Fore femur only 1.15x wider than hind
Howden: Hadromeropsis 97
femur, with slight flange on inner edge distally. Fore tibia
straight; with 12 or 13 small, equidistant teeth. Caudal margins of
ventrites 2, 3, and 4 as in Fig. 218. Ventrite 5 narrow, 1.5x wider
at base than long. Genitalia of paratype as in Fig. 340; spermatheca
almost in one plane, spermathecal duct 2.0 mm long.
Type Series.-Holotype, ECUADOR, Sabanilla, Dr. Ohaus, 1.1907
(Dresden). Paratype, 1 female, ECUADOR, Loja-Zamora, 26-28.X.1977,
2800 m, L. Pefa (Howden).
Remarks.-The paratype differs from the type in the following
respects. Length 10./ mm, width 4.6 mm. Scales of sides of prothorax
similar to those of disc of pronotum (Fig. 217); the two sizes of
scales of elytra almost the same, the larger size white instead of
ochraceous and located only on intervals 1, 2, and 3 medially where
they form a conspicuous streak. Rostrum flat dorsally, lateral edges
more rounded. Long, wispy setae present on elytral intervals 1 and 3
only. Elytra 3.8x longer than prothorax. Fore femur 1.2x wider than
hind femur. Fore tibia with 11 teeth on inner edge.
| The species is very close to impressicollis of Colombia. Series
of both sexes are needed to define the relationships.
The name is based on the Latin word for flounce and refers to the
expanded apex of the elytra.
35. Hadromeropsis (Hadrorestes) bombycinus n. sp.
Figs. 219-222, 225, 341, 342; Map 11
Diagnosis.-Based on unique female (Fig. 220). Entire beetle with
a microsculpture that is very uniform, very minutely granular except
on elytra where it is irregular, coarser, more alutaceous. Head and
Enh te and flat with no other sculpture than the frontal pit
PAG. 422),
Description.-Holotype, female, length 11.4 mm, width 4.9 mm.
Color piceous, very slightly aeneous; legs, antennae and apex of
rostrum reddish; integument with an alutaceous sheen due to the
microsculpture (see head in Fig. 222 and depression of prothorax in
Fig. 219). Head and rostrum as in Diagnosis; dorso-lateral edges more
rounded than they appear in Fig. 222. Side of head and rostrum with
numerous, very fine, prostrate setae or scales of off-white with
Cupreous reflections. Prothorax 1.1x wider than long. Pronotum with
lateral depressions very pronounced, sculptured as in Fig. 219; disc
glabrous except for setae arising from tubercles, a few setae on basal
constriction, and a few minute setae in depressions. Sides of
prothorax with thin line of wider scales forming a vitta; with many
long, wispy. setae. Elytra across humeri 1.6x wider than prothorax;
elytra 3.5x longer than prothorax; elytra 2.3x longer than width
across humeri. Sides gradually divergent to just caudad of middle
where they are 1.3x wider than across humeri, thence gradually rounded
to apex, apical umbone not evident in dorsal outline. Apex of elytra
(Fig. 221) truncate at end of intervals 1 and 2 and with a very brief
tooth. Striae as in Fig. 220. Intervals with tubercles across base,
on intervals 7-10, and on declivity as illustrated; in dorsal view
tubercles silhouetted along entire outline of elytra. Sides of elytra
98 Contrib. Amer. Entesinst., voliei9, no. 6, 1982
(Fig. 225) and declivity sparsely set with minute seta-like scales.
Setae of intervals on disc very sparse, very inconspicuous, appressed,
only a few long, wispy setae on base; setae of sutural interval at
summit of declivity slightly larger, very fine, completely arched.
Fore femur only 1.1x wider than hind femur, distally with vague tibial
groove but no distinct flange on inner edge. Tibiae with the parallel
grooves typical of group reduced. Fore tibia with approximately 10
small sharp teeth. on inner edge. Metasternum sparsely set with small,
round, shiny granules. Ventrite 5 across base 1.5x wider than long.
Genitalia as in Figs. 341, 342; spermatneca almost in one plane;
spermathecal duct 2.3 mm long. ;
Type Series.-Holotype, PERU, Huanuco, Huamincha, 1600 m, Mar.
1946, F. Woytkowski Coll., Donor Wm. Proctor (New York).
Remarks.-Ventrite 5 appeared almost flat before dissection. If it
proves to be flat in future specimens, this would be a_ useful
additional diagnostic character.
The bursa copulatrix appeared particularly tough and muscular; it
was Opaque even after treatment with KOH. Figure 342 shows a ventral
view of the bursa with the inflatable flap and common oviduct pulled
back to reveal the base of the spermathecal duct.
This is a very distinctive species with the integument beautifully
sculptured producing a sheen like that of black silk broadcloth, hence
the name “bombycinus" meaning silken.
36. Hadromeropsis (Hadrorestes) brachypterus n. sp.
Figs. 223, 224, 226-230, 344
Diagnosis.-Based on unique female. Sculpture of prothorax and
elytra composed of crowded, small, uniform tubercles, each bearing a
recumbent, short, white seta. Brachypterous, wing only 0./7x as long
as elytron. Elytra (Fig. 229) inflated medially, 1.4x wider at about
middle than across humeri, thence tapered directly to apex with no
trace of apical umbone. Mesepimeron slender, protuberant (Fig. 226).
Description.-Holotype, female, length 12.5 mm, width 5.4 mm.
Color castaneous; sparsely set with small white setae and seta-like
scales. With no long, wispy setae on dorsal or lateral surfaces, a
few on prosternum and base of femora. Head and rostrum coarsely
rugose (Fig. 223); median line finely impressed between eyes, weakly
carinate on rostrum. Rostrum dorsally almost flat, lateral edges
abrupt. Sides of head and rostrum with scales only very slightly
longer and more numerous. Prothorax (Fig. 227) 1.1x wider than long.
Pronotum with lateral and median depressions replaced by slightly
flattened area; sculpture as in Diagnosis and in Fig. 227. Scutellum
rectangular. Elytra as in Diagnosis and Figs. 228, 229; elytra across
humeri 1.2x wider than prothorax, 3.6x longer than prothorax. Base of
elytra obliquely inclined anteriorly, humeral angle oblique. Only
striae 1-4 discernible on disc, remaining striae irregular and
confused or replaced by tubercles and rugosities. Intervals with very
fine scales or setae, 1-5 abreast, each smaller or larger than the
single white seta at anterior edge of each strial puncture; in
addition with a few larger white scales in a rudimentary subapical
Howden: Hadromeropsis 99
V-shape. Apex of elytron thickened, not ending in tooth (Fig. 228).
In dorsal view tubercles on sides silhouetted along entire outline of
elytra; tubercles rounded, not sharp in outline. Wing as_ in
Diagnosis, without folds. Fore femur (Fig. 224) 1.3x wider than hind
femur; more coarsely sculptured than in impressicollis female; flange
obsolete. Fore tibia with 10 minute teeth on inner edge. Mesepimeron
as in Diagnosis and Fig. 226; paler than surrounding integument, with
about 10 extremely small setae. Metasternum short, 1.7 mm long at
Suture with metepisternum, sculptured as in impressicollis female, its
antero-lateral edge forming a raised lip over adjacent mesosternum.
Abdomen similar to that of institulus; ventrite 5 (Fig. 230) 1.6x
wider than long; apex with a few deep punctures. Genitalia as in Fig.
344. Spermatheca with cornu and ramus bent at an angle; spermathecal
duct 2 mm long; end of duct within bursa copulatrix without obvious
plate.
Type Series.-Holotype, 282, Baly, Bowring Coll. (London).
Remarks.-Although the castaneous color suggests a_ teneral
condition, the dark spermatheca indicates a mature specimen. The
Slender, protuberant mesepimeron, the short metasternum, the
triangular apical half of elytra without an umbone, and the relatively
narrow and oblique base of the elytra, although not extreme, are all
attributes of a flightless species. The meso- and metathorax of
bombycinus (Fig. 225) illustrate the typical appearance of these
structures in a fully winged species. The edge of the apex of the
elytra lacks the denticles typical of Hadrorestes, but this condition
prevails in all three flightless species - see Remarks on striatus.
The few broader scales on the elytra suggest that a pattern may
sometimes occur in this species. The absence of long, wispy setae on
the dorsal surface may be of diagnostic value. The minute teeth on
the fore tibia may also prove to be diagnostic.
Within the ie ee group the male of this species should be
distinguishable by the sculpture of the rostrum and _ prothorax,
possibly also by a protuberant mesepimeron and color.
H. brachypterus lacks several Characteristics of the
impressicollis group: the long, wispy setae of the elytra and sides
and dorsum of the prothorax are absent, the edge of the apex of the
elytra is without denticles, and the usual depressions of the pronotum
are weak. I interpret this to be a secondary loss in a highly derived
species since the sculpture of the tibiae, densely squamose scutel lum,
and dense patches of elongate scales at diagnostic spots on _ the
ventral surface are all well-developed group characteristics.
The transandinus Group
37. transandinus n. sp. | 39. apicalis. n. spy
38. nanus n. sp.
Characteristics of Group.-Small, elongate species, 7.6-11.2 mm in
length. Epistoma wide, rostrum moderately short. Mandible without a
groove on dorsal surface, one or two dorsal setae set in a large
puncture. Eye large. Prothorax with strong basal and apical
constrictions, median line distinctly to conspicuously depressed;
sides of prothorax with sharp tubercles. Scutellum with long whitish
100 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
seta-like vestiture. Postocular vibrissae well developed. Elytra
long, slender, 3.0-4.5x longer than prothorax; flat in lateral view;
Strial punctures very large. Fore femur not greatly enlarged,
posterior face of fore femur of male smooth (male of apicalis not
known). Ventrite 5 of female without lateral depression but may be
flattened (female of nanus not known). Proximal end of internal
sclerite of internal sac strongly reflexed (Figs. 320-323). Apex of
internal sac directed dorsally or distally. Female with flat sclerite
at junction of spermathecal duct within bursa copulatrix.
Remarks.-These three species, closely related to each other, occur
in a transverse band across northern Ecuador. Unfortunately, both
sexes are known for only transandinus and until both sexes are
available for all three species, they must be considered incompletely
diagnosed.
Of the two species represented by males, one has the apex of the
internal sac curved and dorsally directed (transandinus, Fig. 323) and
One has the apex straight and distally directed (nanus, Fig. 321).
The latter is more likely a reduction from a dorsally directed apex
(as in transandinus) than intermediate between the distally directed
apex as in impressicollis and exilis. See Remarks, nanus. The
transandinus group, therefore, apparently derived from a common
ancestor with a pectinatus group species.
37. Hadromeropsis (Hadrorestes) transandinus n. sp.
Figs. 33, 231-234, 305, 322, 323, 343; Map 10
Diagnosis.-Prothorax of male (Fig. 234) with strong basal and
apical constrictions and median line deeply impressed, the latter
forming a "Y" with apical constriction. Elytra with vague to distinct
flattened area behind scutellum. Elytra of female in profile (Figs.
231, 232) with summit of declivity distinct, apex attenuate into a
conspicuous tooth distinctly ventrad of apical umbone. Spiculate apex
of internal sac curved and directed dorsally (Fig. 323).
Description.-Holotype, male, length 9.0 mm, width 3.0 mm. Black,
shiny; with small greenish white scales. Scales of head, rostrum, and
prothorax very sparse, confined to protected areas as around eye and
sides of basal constriction of prothorax. Most scales of elytra in
irregular transverse depressions. Head and rostrum very smooth,
polished, with only a few minute punctures. Rostrum with median line
finely, deeply impressed from between posterior edge of eyes to about
middie, sides rather strongly rounded and deflected to median line.
Segment 2 of funicle slightly longer than segment 1. Prothorax as in
Diagnosis and Fig. 234; 1.05x wider than long, sides only weakly
rounded between constrictions; lateral tubercles acute in dorsal view.
Pronotum with an area on side somewhat flattened and with sculpture
weaker. Elytra across humeri 1.4x wider than prothorax, elytra 3.2x
longer than prothorax. In dorsal view (Fig. 33) sides of elytra
parallel for basal 0.5 thence very gradually convergent to apex,
apical umbone not prominent, just touching outline, apices very
briefly individually rounded. Dorsal outline with obsolete tubercles
on basal 0.2, on apical 0.3 with small, sharp tubercles followed by
Howden: Hadromeropsis 101
denticles on edge of apex. Base of stria 5 and postscutellar area
weakly depressed; apparently without long setae. Sculpture of elytra
similar to Figs. 231, 232 of female; intervals with fine setae each
about as long as adjacent strial puncture, setae becoming longer,
erect apicad and laterad. Fore femur 1.9x wider than hind femur; 1.5x
wider than rostrum; surface very smooth and polished except weakly
sculptured distally; set with fine, erect white setae. Fore tibia
straight; faintly punctulate; inner edge with 10 equidistant teeth,
the central 3 teeth slightly larger; with numerous erect straight or
curved fine dark setae. Middle and hind tibiae with bristles of inner
edge obsolete. Ventrite 5 approximately 2x wider than long, slightly
convex, apex truncate-emarginate. Genitalia of paratypes as in Figs.
322, 323; aedeagus 2.8 mm long.
Allotype, female (Fig. 231), length 10.6 mm, width 3.8 mm.
Differs from type as follows. Antenna, mandible, epistoma and legs in
part reddish yellow. Scales and some setae (especially on hind coxa
and scutellum) iridescent green. Head and rostrum (Fig. 233) more
strongly punctured, rostrum with some punctures coalescing into brief
rugae. Prothorax 1.09x wider than long; median line not impressed,
disc instead rather broadly flattened medially with confluent
tubercles; lateral flattened area scarcely evident. Elytra across
humeri 1.5x wider than prothorax; elytra 3.9x longer than prothorax,
elytra.2.4x longer than width across humeri. In dorsal view sides
Slightly divergent to middle thence very gradually convergent to apex,
apical umbone weakly arcuate in outline; profile as in Diagnosis, Fig.
232. Strial punctures smaller, striae more confused apically by
tubercles; summit of declivity with 4 long setae. Fore femur 1.2x
wider than hind femur, sculpture more pronounced. Fore tibial teeth
uniform in size. Fore tarsi longer (Fig. 305). Middle and hind
tibiae with 5 to 8 stout bristles on inner edge. Caudal surface of
ventrites 2, 3, and 4 equal in height, slightly anteriorly directed,
the edge rounded medially. Ventrite 5 across base 1.4x wider than
long; entire segment slightly convex. Genitalia as in Fig. 343;
spermathecal duct approximately 2.2 mm long.
Type Series.-Holotype, ECUADOR, Pichincha, 10 km E Tandapi, 2000
m, 11.VI.1976, S & J Peck, beating vegetation (Howden). Allotype,
ECUADOR, Napo, 2 km S. Oritoyacu, 22 km S Baeza, 1500 m, III.4-5.1976,
J M Campbell (Howden). Paratypes, 3 males. ECUADOR. Pichincha: 2
males, same data as type (Ottawa, Howden); 1 male, Quito, Coll.
Kuschel (Auckland).
Note: Tandapi appears as Cornejo Astorga on recent maps.
Remarks.-The paratypes are 8.5-10.5 mm in length and 2.8-3.4 mm in
width. They vary from the type as follows. Rostrum with a few brief
rugae. Prothorax with sides more strongly rounded in some, 1.01-1.08x
wider than long. Elytra 3.0-3.5x longer than prothorax, apical umbone
arcuate in dorsal outline.
The name transandinus refers to the fact that the species is known
from both the Pacific and Amazonian slopes of the Andes.
102 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
38. Hadromeropsis (Hadrorestes) nanus n. sp.
Figs. 238, 320, 321; Map 10
Diagnosis.-Based on unique male. Very small. Base of elytra
evenly convex in scutellar area. Fore femur slender, approximately as
wide as rostrum. Endophallic structures large, larger than in
transandinus; spiculate apex short, straight (Fig. 321).
Description.-Holotype, male, length 7.6 mm, width 2.5 mm. shiny
black; antenna, epistoma, mandible and legs reddish yellow. Sparsely
set with round scales of slightly iridescent pale blue or whitish;
scales more numerous than in transandinus, on ventral surface almost
as numerous as on dorsum, occurring even on fore coxa and base of fore
femur. Head and rostrum (Fig. 238) sparsely punctate, median line
finely impressed from frontal fovea to anterior edge of eye, entire
rostrum longitudinally concave. Segment 2 of funicle 1.4x longer than
segment 1. Prothorax (Fig. 238) 1.09x wider than long, similar to
that of transandinus. Elytra cylindrical, as in Diagnosis. Elytra
across humeri I.3x wider than prothorax, elytra 3.6x longer than
prothorax, elytra 2.4x longer than width across humeri. In dorsal
view sides of elytra parallel on basal 0.13, feebly rounded, thence
very slightly convergent to apical umbone, apex broadly rounded from
between striae 5, apices briefly divergent. Dorsal outline with no
tubercles from base to apical 0.3, thence with small, acute tubercles
similar to denticles of apical edge of elytra. Stria 5 weakly
depressed at base. Base of elytra with several rows of long, wispy
setae. Sculpture of elytra, strial punctures similar to those of
transandinus, striae more confused by more numerous squamose
depressions. Setae of lateral intervals longer, more conspicuous,
especially on declivity. Fore femur 1.3x wider than hind femur, as
wide as full width of rostrum; distal flange very weak; sculpture of
femur obsolete; setae of femur very conspicuous, long, white, erect.
Fore tibia weakly bowed distally, obsoletely punctate, inner edge with
8 or 9 very small, uniform teeth; with numerous long, curved and some
long, straight erect setae. Middle tibia with row of 4 or 5, hind
tibia with 2 or 3 bristles on inner edge. Ventrite 5 across base 1./x
wider than long, slightly convex, apex truncate-emarginate. Last
tergite with inflexed apex (lip) short. Genitalia as in Figs. 320,
321, and Diagnosis; aedeagus 2.4 mm long.
Type Series.-Holotype, ECUADOR, Pichincha, km 27, Old Santo
Domingo Rd, 3200 m, 18.11.1979, H. Howden, on alder (Howden).
Remarks.-The erect setae of the fore legs are particularly
conspicuous, as are the long, wispy setae of the base of the elytra;
on older specimens, they would be less conspicuous from wear.
Because of the extremely small size and delicate proportions of
the type specimen, the narrow fore femur might be attributed to
allometric growth. However, allometric growth could not account for
the convex base of the elytra nor the large, very distinctive
endophallic structure. The short, straight, distally directed apex of
the internal sac is apparently a reduction from a dorsally directed
form since the internal sclerite is very large and strongly reflexed
proximally.
In addition to the diagnostic characters listed, nanus differs
Howden: Hadromeropsis 103
from transandinus in the setae at the base of the elytra numerous and
long, teeth of the fore tibia very fine and uniform, and the elytra
more cylindrical in caudal view.
Since nanus shares many characters with apicalis, including a more
dorsal apex of elytra and similar habitat in Ecuador, the suspicion
exists that they may be male and female of the same species. However,
from the evidence on hand, I feel they are separate taxa. The base of
the elytra at the scutellum is so completely convex in nanus that it
is unlikely to be depressed in the opposite sex.
39. Hadromeropsis (Hadrorestes) apicalis n. sp.
Figs. 30, 235-237, 345; Map 10
Diagnosis.-Based on female only. Similar to female of
transandinus, but with a pronounced aeneous lustre; elytral declivity
very brief, attenuate apex of elytra in lateral view thus close to
dorsal surface; elytral 4.0-4.5x longer than prothorax.
Description.-Holotype, female, length 11.2 mm, width 3.6 mm.
Shiny black with aeneous lustre; femora, antenna, mandible, and
epistoma piceous. Sparsely clothed with off-white or pale greenish
scales of small size. Head and rostrum as in transandinus female.
Prothorax as in Fig. 236; 1.1x wider than long; sides moderately
rounded between constrictions; basal constriction narrow, complete
dorsally; apical constriction obsolete on disc. Pronotum flattened
along median line, here irregularly transversely sculptured; either
Side of this area punctate, almost smooth, gradually changing to
distinct, discrete tubercles on vertical sides. Elytra (Fig. 30)
across humeri 1.5x wider than prothorax, elytra 4.0x longer than
prothorax. In dorsal view humeri very prominent, sides subparallel
for basal 0.3, thence broadly rounded to apical umbone, the umbone
weak; sides of apex slightly sinuate from beneath stria 4; apices
briefly attenuate, slightly inwardly directed. Ventrally (Fig. 237)
apical attenuation expanded beyond border of elytra which remains
parallel to stria 10. Dorsal outline with small tubercles on basal
0.25, conspicuous tubercles on apical 0.5. Base of stria 5 impressed;
with distinct postscutellar flattened area; with some moderately long,
tapered setae. Setae of intervals becoming longer toward sides and
apex. Fore femur 1.2x wider than hind femur; fore femur with moderate
flange, its edge weakly serrulate; weakly sculptured with faintly
impressed honeycomb lines changing to impressed longitudinal lines
distally. Fore tibia straight with 11-13 small teeth; outer edge
Sparsely punctate. Middle and hind tibiae with 5-8 stout bristles on
inner edge. Caudal surface of ventrites 2, 3, and 4 equal in height,
Slightly anteriorly directed. Ventrite 5 (Fig. 237) across base 1.5x
te than long. Genitalia as in Fig. 345; spermathecal duct 2.0 mm
ong.
Type Series.-Holotype, ECUADOR, Napo, 4 km W Papallacta, 3200 mn,
LL.D J. M. Campbell (Howden). Paratype, 1 female, ECUADOR,
Chimborazo et Pichincha, Mandeville, 272, 1853 (Paris).
Remarks.-The paratype is 11 mm long and 4.2 mm wide. It differs
from the type in the following respects. Sculpture of head (Fig. 235)
104 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
more complex. Prothorax almost uniformly tuberculate. Elytra across
humeri 1.2x wider than prothorax, elytra 4.5x longer than prothorax,
elytra 2.5x longer than width across humeri. Elytra in profile
slightly concave medially. Apex much more developed; sutural interval
at summit of declivity with 2 or 3 long setae (these abraded in type).
Metasternum and ventrites 1 and 2 with a fine microsculpture of
parallel, transversely impressed lines.
The flared and attenuate apex of the elytra (Fig. 237), for which
the species is named, is of a different origin than that of institulus
(Fig. 218) in which the margin is simply crimped outwardly, stria 10
following the margin closely.
In addition to the diagnostic characters, apicalis differs from
transandinus in the very prominent humeri and the more conspicuous
tubercles of the elytra in dorsal outline. H. apicalis occurs at a
much higher elevation than transandinus, its range bisecting the
lower-elevation range of transandinus. H. nanus occurs in a habitat
similar to that of apicalis; see Remarks of that species.
The pectinatus Group
40. dialeucus n. sp. 45. magicus (Pascoe)
41. contractus n. Sp. 46. nitidus n. sp.
42. pectinatus n. sp. 47. mandibularis n. sp.
43. conquisitus n. sp. 48. spiculatus n. sp.
44, scambus n. sp.
Characteristics of Group.-Proximal end of internal sclerite within
internal sac strongly reflexed (Figs. 324-328). Apex of internal sac
produced in a curved, dorsally directed, short to greatly elongated
cone or tube. Dorsal surface of internal sac above proximal end of
heavy internal sclerite without a cupped inflatable lobe. Junction of
spermathecal duct inside bursa copulatrix unmarked or with a faint
small sclerite.
Remarks.-The species are arranged here according to the length of
the apex of the internal sac and spermathecal duct. It then becomes
evident that the species are similarly. related in other features as
well.
Both sexes are known for six of the nine species.
In addition to the obvious similarities in the male genitalia, the
sculpture on the posterior face of the fore femur of the male shows a
close relationship between impressicollis and the first few species in
this group. In these species the distal tubercles are grossly
enlarged into a shelf, the large seta-bearing surface flat or concave
and abruptly perpendicular to the surface of the femur. A _ lesser
development of these shelf-like tubercles is seen in the lower right
corner of Fig. 25/7.
In the remaining species there is a trend for the overall
sculpture of the beetle to gradually decrease as the genitalia becomes
more extreme.
Howden: Hadromeropsis 105
40. Hadromeropsis (Hadrorestes) dialeucus n. sp.
Figs. 28, 279, 281, 307, 324, 325, 355
Diagnosis.-Female elytra clothed (a) with small to minute scales
clustered in irregular transverse depressions; (b) sometimes also
patterned with basal oval ring, median fascia, and apical lunule of
white scales of varying sizes (Fig. 28), or with fragments of this
pattern; or, (c) with pattern of (b) but remainder of elytra densely
covered with ochraceous, sometimes imbricate, larger (0.1 mm) scales.
Prothorax (Fig. 281) with rounded tubercles of sides obsolete or
completely absent on disc, disc almost smooth and shiny in some.
Elytra of female with sides very gradually rounded to apex from about
middie. Posterior half of hind coxa covered with rounded, separated,
moderate-sized, whitish or ochraceous scales. Male with internal sac
Similar to that of pectinatus but apex lacking the pair of sclerotized
dorsal lobes (Fig. 325).
Description.-Holotype, male, length 11.0 mm, width 3.8 mm.
Reddish except head and base of elytra black. Appearing glabrous
macroscopically; body dorsally and ventrally with minute, round, oval,
or elongate white scales (visible in Figs. 279, 281); scales of
posterior half of hind coxa as in Diagnosis, larger than any others
but not full-sized. Head and rostrum similar to those of spiculatus
in Fig. 288, with distinct scattered punctures, a few confluent
punctures on rostrum forming brief rugae; median line briefly, finely
impressed, with small frontal fovea. Funicle with segments 1 and 2
equal in length. Prothorax 1.1x wider than long, sides moderately
rounded, widest behind middle. Pronotum with median line distinctly
impressed basally, disappearing before apex; sculpture otherwise as in
Diagnosis; setae as in pectinatus. Elytra across humeri 1.3x wider
than prothorax; elytra 3.0x longer than prothorax. Elytra shaped as
in pectinatus except apex less truncate. Elytral striae and sculpture
Similar to that of pectinatus but striae more distinct, intervals
smoother, tubercles at base of elytra weaker. Fore femur 2.1x wider
than hind femur; posterior face with about 17 shelf-like tubercles,
these weaker than in pectinatus; sculpture of fore femur and tibia
Otherwise similar to that of pectinatus. Inner edge of fore tibia
with 10 or 12 nearly iii ton STORE WEBER, Fore tarsus (Fig. 307)
Similar to that of pectinatus but shorter. Middle and hind tibiae
without tubercles, with I or 2 stout bristles. Abdomen with punctures
obsolete except on apical half of ventrite 5; ventrite 5 across base
2.2x wider than long. Aedeagus (Fig. 324) 3.1 mm long, aedeagal
ohare Phd mm, tegminal strut 1.8 mm. Internal sac. as in Diagnosis,
Fig. ;
Allotype, female, length 12.3 mm, width 5.0 mm. Differs from type
as follows. Most of integument black, legs and antenna reddish.
Scales more numerous on both dorsal and ventral surfaces; elytra
patterned as in Fig. 28 and Diagnosis, but some scales abraded,
pattern recognizable by scars. Pronotum smoother (Fig. 281). Elytra
across humeri 1.5x wider than prothorax; elytra 3.6x longer than
prothorax. In dorsal view (Fig. 28) sides of elytra very slightly
divergent to about middle where they are only 1.2x wider than across
humeri, very gradually convergent to apex (Fig. 279), apical umbone
106 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
weak, just touching dorsal outline. Sutural interval produced into
very brief, caudally projecting tooth. In profile elytra more convex
basally, gradually curved to summit of declivity which is scarcely
perceptible, marked with 7-8 long, reddish setae. Fore femur 1.3x
wider than hind femur; posterior face lacking shelf-like tubercles;
teeth of fore tibia very small. Middle and hind tibiae with 1-3
Strongly oblique bristles, no tubercles. Ventrites 3, 4, and 5 with
rough sculpture at sides. Caudal surface of ventrites 2 and 3
moderate, smooth, shiny, anteriorly slanted; caudal surface of
ventrite 4 almost perpendicular, moderate in height, straight in-
posterior view. Ventrite 5 across base 1.8x wider than _ long.
Genitalia of paratypes as in Fig. 355; spermathecal duct 1.8 mm long.
Type Series.-Holotype, no data, green square of paper (Oxford).
Allotype, VENEZUELA, Coll. C. Felsche, Kauf 20, 1918 (Dresden).
Paratypes, 6 females. VENEZUELA. 1 female, same data as allotype
(Dresden); 1 female, Coll. Kuschel (Auckland). No locality: 4
females, no data (Berlin, London, Howden).
Remarks.-Females vary in length from 11.3-12.5 mm and in width
from 4.5-5.0 mm. In the maximum vestiture (one female) only the basal
ring and median fascia are present; these markings conspicuous,
glabrous (hence black) but with the center of the markings set with
small, faintly opalescent scales; remainder of elytra and line on base
of prothorax with larger (0.1 mm), often imbricate, pale ochraceous
scales; head, rostrum, prothorax except basal line, elytral humerus,
and legs with the smaller faintly opalescent scales; ventrally with
ochraceous scales very sparse medially. The minute scales are
definitely greenish on the elytral declivity in one female. Elytral
setae are very slender, translucent brown or paler, up to 0.5 mm long
on lateral intervals of elytra; slightly thicker and white on the
Sides of the prothorax and meso- and metasterna.
In addition to the diagnostic characters, dialeucus differs from
pectinatus in the shorter aedeagus and the lack of tubercles on the
middle tibia.
The name means "marked with white”.
41. Hadromeropsis (Hadrorestes) contractus n. sp.
Figs. 3/7, 274-278, 354; Map 12
Diagnosis.-Based on female only. Elytral pattern as in Fig. 37.
Ventrites 3, 4, and 5 much narrower than ventrites 1 and 2; adjacent
elytral margins likewise convergent and attenuate. Caudal surface of
ventrite 4 strongly produced in a high arc, strongly to moderately
posteriorly slanted. Apical fourth of fore tibia abruptly bent
inward.
Description.-Holotype, female, length 11.3 mm, width 4.3 mm.
Integument shiny black except legs and antenna reddish. Dorsally
Sparsely but evenly clothed with small, round, pale greenish white
scales in depressed areas. Elytra also with larger, round, white
scales forming a faint basal arc, a median fascia and an apical
lunule. All setae opaque white, longest on abdomen and metasternun,
Shortest on disc of elytra. Head and rostrum (Fig. 274) slightly
Howden: Hadromeropsis 107
concave, with punctures and some small depressions; median line finely
impressed, frontal fovea obsolete. Funicle with segments 1 and 2
equal in length. Prothorax (Fig. 275) 1.1x wider than long; sides
moderately rounded between constrictions; covered with low, round
tubercles which become weaker medially; median line not marked; space
between tubercles with scales. All setae of sides and disc of
prothorax recumbent. Elytra across humeri 1.4x wider than prothorax;
elytra 3.6x longer than prothorax. Elytra in dorsal view (Fig. 37)
with sides slightly divergent to about middle thence convergent in
Straight line to apex, apical umbone interrupting this line in a
conspicuous arc. Apex of elytra (Fig. 2/77) in dorsal view
conspicuously narrow and attenuate, each elytron terminating in short
tooth. Dorsal surface of elytra without long, wispy setae, without
tubercles, basal portion of elytra with shallow, sinuous, transverse
depressions; strial punctures deep, mostly regularly aligned except in
white markings. Declivity and intervals 8, 9, and 10 with moderate to
weak acute tubercles each with a short, white seta; tubercles obsolete
on middle of sides. Fore femur (Fig. 276) 1.7x wider than hind femur;
femur with fine netted microsculpture, distal portion of femur and all
of fore tibia with deeply impressed parallel grooves; without long,
wispy setae (possibly only a female characteristic), nowhere with
tubercles, inner edge with very weak flange. Fore tibia as in
Diagnosis and Fig. 2/6; with 11 small, equal equidistant teeth on
inner edge. Middle tibia with 4, hind tibia with 1, strongly oblique
bristles. Hind coxa with no scales, only white setae. Abdomen as in
Diagnosis and Fig. 278. Ventrites 3, 4, and 5 with numerous, long,
white setae; caudal surface of ventrites 2 and 3 finely rugulose;
caudal surface of ventrite 4 smooth and shiny. Ventrite 5 only 1.4x
wider than long, lateral concavities very deep and large. Genitalia
of paratypes (including two examples of lateral sclerite) as in Fig.
354; no sclerite at junction of spermathecal duct with bursa
copulatrix; spermathecal duct 1.6-1.9 mm long.
Type Series.-Holotype, female, BOLIVIA, Coroico, Ost Bolivien,
1913, 16 (Dresden). Paratypes, 2 females, BOLIVIA, Coroico,. EX.:¢ol};
Clerc (Paris).
Remarks.-The two paratypes are 11.4-12.4 mm long and 4.5-4.7 mm
wide. They differ from the type in having the median line of the
pronotum marked by an obsolete or partial impression, the apical
umbone of the elytra less prominent, the elytra more strongly
sculptured, and the striae consequently less distinct.
Superficially contractus resembles dialeucus but the conspicuously
narrowed, attenuate apex of the elytra, the more strongly sculptured
prothorax, and the non-squamose hind coxa readily distinguishes
contractus. Series of both sexes of both species are needed to
establish inter- and intraspecific variation.
This species is perhaps most closely related to pectinatus, the
female of which differs in the broader, more gradually narrowed
abdomen; more erect, longer, and more slender setae of intervals 8, 9,
and 10 and declivity; more distinct declivity; absence of large scales
dorsally; more strongly sculptured caudal surface of ventrites 2 and
3; less arcuate caudal margin of ventrite 4; and less bowed fore
tibia.
The name, contractus, refers to the contracted ventrites 3, 4, and
108 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
42. Hadromeropsis (Hadrorestes) pectinatus n. sp.
Figs. 35, 265-270, 308, 328, 352; Map 13
Diagnosis.-Neither sex with full-sized scales either dorsally or
ventrally. Prothorax (Fig. 266) with sculpture composed of very
uniform, rounded tubercles evenly distributed over all, including (in
male) the narrowly depressed median line. Female with sutural edges
of elytra separated apicad of interlocking flange, produced into
strongly convergent teeth (Fig. 268). Fore femur of male on its
posterior face distally with 6 to 24 well-developed shelf-like
tubercles each bearing a long, wispy seta in its saucer-like follicle.
ipa eh of male with 3 or more teeth of inner edge extremely long
Pagec267)%
Description.-Holotype, male, length 11.5 mm, width 4.1 mm. Black
except antenna, prothorax and base of fore coxa and fore femur
reddish; with minute blue scales scattered over dorsum and very
Sparsely over ventral surface, scales of prothorax elongate, others
rounded. Head and rostrum (Fig. 265) dorsally and laterally with deep
punctures, some elongate and confluent forming short rugae; frontal
fovea small; median line weakly impressed. Rostrum narrow, dorsally
shallowly concave, sides flared outward apicad of antennal insertion;
dorso-lateral edges prominent. Funicle with segment 2 slightly longer
than segment 1. Prothorax as in Diagnosis and Fig. 266. Prothorax
1.1x wider than long, sides strongly rounded between constrictions;-
each tubercle with a very slender white seta, setae shorter dorsally
and towards median line; no long, wispy setae visible dorsally but
some setae of basal constriction on sides less curved. Elytra (Fig.
35) across humeri 1.3x wider than prothorax; elytra 3.0x longer than
prothorax. Elytra in dorsal view with sides parallel to just caudad
of middle, thence gradually rounded to apex, apical umbone obsolete
and not entering dorsal outline, apex truncate. Base of elytra not
depressed at stria 5, weakly depressed behind scutellum, base of
dorsal intervals with short row of tubercles; each tubercle bearing a
fine, long, wispy straight or curved seta, additional setae present as
well. All lateral intervals and entire declivity with numerous acute
tubercles, entire dorsal outline of elytra "dentate" from the profile
of these tubercles; each tubercle bearing a conspicuous, long,
Straight or weakly curved seta. Striae distinct centrally only,
remainder of disc with short to long, transverse squamose depressions
about half as deep as strial punctures, these transverse depressions
Shorter caudad and changing until before declivity each interval with
series of tubercles extending the width of interval and each strial
puncture separated by a small tubercle. Fore femur 2.2x wider than
hind femur; anterior face with fine netted microsculpture which
distally becomes deeply impressed parallel grooves with scattered deep
punctures superimposed, each puncture bearing a long, wispy seta;
inner edge of fore femur with very weak distal flange; inner surface
including tibial groove with scattered tiny granules; posterior face
as in Diagnosis. Fore tibia (Fig. 267) slightly curved with 10-12
Howden: Hadromeropsis 109
slanting teeth on inner edge, the 3 distad of middle extremely long
(badly worn in type); fore tibia densely sculptured with deep rugae
and punctures. Fore tarsus with segment 1 long, parallel-sided (Fig.
308). Middle and hind tibiae with row of tubercles on inner edge, 2
or 3 most distal tubercles each with a stout bristle arising from
base. Abdomen with very fine scattered punctures on ventrites 1 and
2, punctures larger and denser on ventrites 3-5, apex of ventrite 5
very broadly truncate-emarginate. Genitalia similar to Fig. 324 of
dialeucus, aedeagus 4.0 mm long. Apex of internal sac (Fig. 328) with
pair of distinct sclerotized lobes slightly dorso-laterally directed
(marked with arrow in figure). |
Allotype, female, length 12.3 mm, width 5.0 mm. Differs from type
as follows. Only base of pronotum reddish; scales white. Rostrum
wide; only briefly concave apically, sculpture of head and rostrum
finer. Prothorax with sides less strongly rounded, tubercles weaker,
median line not marked except by break in tubercles. Elytra across
humeri 1.5x wider than prothorax, elytra 3.6x longer than prothorax.
Elytra in dorsal view with sides gradually divergent to just beyond
middle where they are 1.2x wider than across humeri, thence gradually
rounded to apical umbone which is smal] but distinct in outline, apex
approximately triangular. Sutural edges of elytra as in Diagnosis,
Fig. 268. Declivity in profile slightly concave, sutural edge at
summit of declivity with 4 very long setae. Fore femur 1.4x wider
than hind femur; posterior face lacking shelf-like tubercles. Fore
tibia on inner edge with 8 or 9 more erect teeth, the 3 distad of
middle shorter than in type but longer than in males of many species.
Base of ventrites 3, 4, and 5 with rather coarse microsculpture (Fig.
269). Caudal surface of ventrites 2 and 3° approximately
perpendicular, coarsely sculptured (Fig. 270); caudal surface of
ventrite 4 smooth, concave; edge medially straight, not as high as
ventrites 2 and 3, directed caudad. Ventrite 5 across base 1.6x wider
than long, strongly medially convex from basal fourth. Genitalia as
in Fig. 352; spermathecal duct 2.6 mm long.
Type Series.-Holotype, PERU, Cuzco, Valle de Lares, 75 km NW
Calca, 2060 m, 6 Feb. 1979, W. E. Steiner (Washington, USNM Type No.
100193). Allotype, same data as type except 13 Jan 1979 (Washington).
Paratypes, 5 males. BOLIVIA: 1 male, Limbo-Chapare, 11.1952, 2000 m
(Howden); 1 male, Yungas, Coll. Kuschel (Auckland). COLOMBIA. 2
males, F. C. Nicholas Collection (New York). PERU. Cuzco: 1 male,
Same data as type (Howden).
Remarks.-The paratypes (all males) range in length from 11.2-14.6
mm and in width from 2.7-5.0 mm. The paratypes exhibit both deeper
and shallower rostral sculpture than the type. The Colombian
specimens differ in the elytral striae more distinct, even on the
declivity. Variation in the number of shelf-like tubercles on the
posterior face of the fore femur is apparently related to development
Of the specimen and not to geographical range. For instance, in the
11.9 mm specimen from Bolivia there are 7-12 shelf-like tubercles
whereas in the 14.6 mm specimen from Bolivia there are 24 shelf-like
tubercles. The hind tibia usually has a single groove on the outer
edge, but it can vary from one side of the beetle to the other. In
all the males there is a trace of the strong microsculpture of the
female abdomen. The aedeagus ranges from 3.8-4.5 mm long in the
110 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
paratypes, but the apex of the internal sac is very uniform.
When looking at mixed species, the very uniform sculpture of the
pronotum and the extremely long teeth of the fore tibia are
particularly conspicuous.
There are two females from Cochabamba, Bolivia, in the Kuschel
collection (Auckland) that may be pectinatus. They are clothed
dorsally and ventrally with small (0.06 mm) round, blue-green,
slightly iridescent scales which are concentrated in depressed areas
On the prothorax and elytra, absent medially on the abdomen. The
thoracic sculpture is considerably weaker than in the type series and
the tibial teeth are uniform. Association with males is required to
establish the identity of these specimens.
The specimens from Peru were part of a small group of specimens on
a legume-like small tree; the remainder of the group dropped when the
collector approached and were not recovered.
The comb of long teeth of the fore tibia suggested the name
“pectinatus'.
43. Hadromeropsis (Hadrorestes) conquisitus n. sp.
Figs. 34, 254-259, 329, 330, 350; Map 12
Diagnosis.-Glabrous or sparsely clothed with scintillating
iridescent green scales. Segment 2 of funicle much longer than
segment 1. Apical umbone of elytra protuberant, set with acute,
caudally directed tubercles (Figs. 34, 254). Fore femur of male
(Figs. 257, 258) with well-developed flange on inner edge distally,
with sharp tubercles on the flange, rounded tubercles on inner surface
except tibial groove. Fore tibia both sexes almost smooth with very
few scattered small punctures; with a few fine, pale, recumbent setae;
fore tibia distally absolutely straight in female and less-developed
in males, slightly bowed in well-developed males (Fig. 258). Internal
sac Of male at extreme apex without 4 inflatable lobes (Fig. 330).
Description.-Holotype, male, length 13.4 mm, width 4.2 mm. Black;
Sparsely clothed in depressed areas with minute green scales. All
dorsal setae very fine and inconspicuous, white, curved. Head and
rostrum with strong median concavity extending to between middle of
eyes; median line finely impressed between apical half of eyes;
dorso-lateral edges of rostrum prominent, rounded, smooth and shiny.
Head and sides of rostrum weakly sculptured with punctures; confluent
punctures or brief rugae on frons. Segment 2 of funicle 1.6x longer
than segment 1. Prothorax (Fig. 255) as wide as long, sides almost
parallel, slightly swollen over fore coxae. Prothorax with sculpture
composed of rounded tubercles, medially tubercles slightly larger and
some confluent; median line finely, partially impressed, crooked. In
profile, pronotum almost flat, except immediately before basal
constriction; basal constriction very short on disc. Elytra across
humeri 1.3x wider than across prothorax, elytra 3.0x longer than
prothorax. In dorsal outline sides of elytra slightly convergent from
humeri, more strongly so from apical third, umbone right-angled, apex
rounded. In dorsal view tubercles of lateral intervals acute on basal
third, absent medially, prominent and acute on umbone; teeth of apical
Howden: Hadromeropsis bit
edge of elytra prominent, even; apices of elytra not at all produced.
Base of elytra depressed at stria 5; elytra moderately concave behind
scutellum. Elytra irregularly sculptured with rounded tubercles
across base; tubercles reduced, becoming confluent on outer intervals
of disc, before declivity becoming low swellings strongly caudally
directed, as wide as interval; much smaller on declivity. Striae 1,
2, and 3 regularly punctate on disc; other striae confused by
sculpture and extra punctures. Fore femur as in Diagnosis and Figs.
25/, 258; enormously swollen, 2./x wider than hind femur. Inner
surface of fore femur with multiple shiny, small round tubercles
except in smooth tibial groove, each tubercle with long, wispy seta;
remaining surfaces of fore femur proximally very finely sculptured,
with only white or greenish, short recumbent setae; posterior surface
strigulate distally. Fore tibia as in Diagnosis and Fig. 258; inner
edge with multiple rounded tubercles and long, wispy setae. Fore
tarsus with segment 1 long and parallel-sided, segments 2 and 3
subequal in length, 0.8 as long as segment 1. Middle and hind tibiae
_ with row of 4-7 tubercles on inner surface near edge, a stout bristle
arising from base of each. Abdomen smooth and shiny, almost
impunctate; ventrite 5 across base 2.0x wider than long, apex broadly
truncate-emarginate. Genitalia as in Figs. 329, 330, and Diagnosis.
Allotype, female, length 13.1 mm, width 5.0 mm. Differs from type
as follows. Clothed on dorsal and ventral surfaces and legs with
scintillating green scales; black integument shining through naturally
(i.e., not abraded) on dorso-lateral edges of rostrum and on elytra
forming pattern (Fig. 34) of a black "S" basally and an oblique
preapical fascia. Scales sparse on disc of pronotum’ which
consequently appears darker. Prothorax slightly wider than long,
sculpture slightly weaker. Elytra across humeri 1.4x wider’ than
across prothorax, elytra 3.4x longer than prothorax. Elytra in dorsal
View widest just caudad of middle; apex beyond umbone more elongate;
apices individually attenuate into conspicuous’ tooth. Sutural
interval at summit of declivity with 3 and 4 long, erect setae. Fore
femur 1.4x wider than hind femur, distal flange greatly reduced but
still evident and its edge denticulate; remaining tubercles obsolete
or absent. Fore tibia with single row of teeth instead of tubercles.
Abdomen with very faint microsculpture similar to that of pectinatus.
Caudal surface of ventrites 2, 3, and 4 approximately perpendicular,
smooth and shiny. Ventrite 5 across base 1.6x wider than long.
Genitalia as in Fig. 350; spermathecal duct of allotype and paratypes
2.4-3.0 mm.
Type Series.-Holotype, ECUADOR [Zamora-Chinchipe], Sabanilla,
15.1X.-/7.X.1905, Dr. Ohaus, 1, 1907 (Dresden). Allotype, same data as
type (Dresden). Paratypes, 2 males, 3 females. ECUADOR. 1 female,
52286, Buckley, Fry Coll. 1905-100 (London); 2 males, 1 female
[Morona-Santiago], Macas, Buckley (Berlin [1 female]; Fry Coll.
1905-100, London [2 males]); 1 female, same data as type (Dresden).
Remarks.-Both male paratypes are 12.1 mm long, 3.8 mm wide; the
three females are 14.0-15.3 mm long, 5.2-5.8 mm wide. The two males
are clothed with full-sized scales and are patterned with glabrous
lines as in the allotype, but the scales appear to be less dense than
in the squamose females. One female is almost glabrous, bearing
minute scales (as in the holotype) on the declivity only, the hind
112 Contrib. Amer, Ent. Inst., vol. 19, no. 6, 1982
coxae having larger elongate green scales. Funicular segment 2 is
always much longer than segment 1, ranging from 1.2-1.7x longer in
females, and 1.6x in all three males. The prothoracic sculpture is
weaker in the squamose paratypes (Fig. 256). The elytral tubercles
are much less developed in one male. The sutural interval on the
summit of the declivity is abraded in all males, they may or may not
have one or two slightly longer setae there; in females 2-8 setae are
present. The fore femur is always enormously swollen in males,
ranging from 2.4-2./x wider than the hind femur, and only 1.4-1.7x
wider in the females.
Three females were dissected; in one (the allotype) the
Spermathecal duct ends in the bursa copulatrix in a distinct spherical
dark bulb. In the second a separate sclerite is seen beneath the duct
near its end within the bursa. In the third a portion of the end of
the duct within the bursa is enlarged and dark.
One of the male paratypes is an old, worn specimen missing its
abdomen; the other is teneral with the aedeagus very callow and I was
not successful in extracting the internal sac from it. This is
especially unfortunate in view of the slight difference noted between
this species and scambus in the apex of the internal sac.
The prominent elytral umbone and characters of the fore legs will
readily distinguish this species. In addition, glabrous specimens can
be distinguished from many species the same size by the absence of
long free-standing setae on the elytra. The squamose specimens are
especially distinctive and can be confused only with scambus. See
discussion of scambus for further comparisons.
Buckley at Macas and Ohaus at Sabanilla collected the entire type
series. The name conquisitus means "sought out eagerly" and refers to
the efforts of these two early collectors.
44. Hadromeropsis (Hadrorestes) scambus n. sp.
Figs. 32, 260-264, 326, 351; Map 13
Diagnosis.-Similar to conquisitus but segment 2 of funicle
Subequal to segment 1; fore tibia with deep confluent punctures and
curved dark, wiry setae; and fore tibia distally strongly bowed. Fore
femur of male with distal flange very weak, without tubercles except
minute ones on flange, no modification below tibial groove. Internal
sac Of male at extreme apex with circle of 4 equal, equidistant
inflatable lobes (Fig. 326).
Description.-Holotype, male, length 9.9 mm, width 3.1 mm. Head
and prothorax black, remainder of body shading to piceous. Sparsely
clothed with minute, scintillating green scales except on legs. All
dorsal setae very fine and inconspicuous; recumbent, less so on
declivity. Head and rostrum similar to conquisitus but median
concavity shallower, median line finely impressed to behind eye.
Segment 2 of funicle 1.1x longer than segment 1. Prothorax 1.04x
wider than long, similar to conquisitus. Elytra across humeri 1.3x
wider than prothorax, elytra 2.6x longer than prothorax. In dorsal
Outline sides of elytra subparallel, gradually converging caudad of
middie, apical umbone weak in outline, apex brief, rounded (Fig. 261).
Howden: Hadromeropsis 113
In dorsal outline tubercles of lateral intervals obsolete or absent
on basal 0.7, small but distinct on apical 0.3, those of umbone small
(Fig. 261), same size as those of declivity and edge of elytra. Base
of elytra at stria 5 and postscutellar area only obsoletely depressed.
Base of elytra without tubercles; strial punctures completely regular,
with only minimal confusion on declivity. Fore tibia and femur as in
Diagnosis and similar to Fig. 262 of female; fore femur 2.2x wider
than hind femur; distal half with wiry setae as on tibia. Fore tarsus
as in conquisitus. Middle and hind tibiae with bristle-bearing
tubercles much less developed than in conquisitus. Abdomen relatively
longer and narrower than in conquisitus, ventrite 5 across base 1.8x
wider than long; apex of ventrite 5 emarginate. Genitalia as in Fig.
326 and Diagnosis. Aedeagus 3.15 mm long.
Allotype, female, length 12.8 mm, width 3.0 mm. Differs from type
as follows. Rostrum more robust (Fig. 263). Prothorax more robust,
1.1x wider than long, disc flat, not at all depressed; in profile
basally much thicker (Fig. 264); setae larger, especially on sides.
Elytra across humeri 1.4x wider than prothorax, elytra 3.4x longer
than prothorax. In dorsal view (Fig. 32) sides of elytra slightly
wider at middle, gradually narrowed to apex, apical umbone rounded in
Outline, apex almost triangular, individual apices not at all toothed.
With weak tubercles on apical portion of intervals 5, 6, and 7 and on
umbone (Fig. 260). Setae of intervals 9 and 10 much longer on apical
half of elytra; summit of declivity with 4-6 long setae. Fore femur
1.5x wider than hind femur. Caudal surface of ventrite 2 distinctly
anteriorly arcuate, of ventrite 3 less arcuate, of ventrite 4 almost
perpendicular; caudal surface of all smooth and shiny. Ventrite 5
across base 1.5x wider than long. Genitalia as in Fig. 351; lateral
sclerite divided into 2 separate pieces; spermathecal duct slightly
thicker just before and throughout bursa; duct broken, more than 1.5
mm long.
Type Series.-Holotype, ECUADOR [Zamora-Chinchipe], Sabanilla,
15.1X.-2.X,05; 1.1907, Dr. Ohaus (Dresden). Allotype, same data as
type (Dresden). Paratype, 1 female, Sarayacu*, Pascoe Coll. 93-60
(London).
*NO country given. It is uncertain whether this is the Ecuadorian
Sarayacu where Buckley collected (Brown, 1941:846) or the Peruvian
Sarayacu from which Kirsch (1873:124) described material in the
Abendroth collection.
Remarks.-The paratype is 13.0 mm long, 5.0 mm wide. It is clothed
with full-sized scintillating green scales much as in conquis i tus
except the sinuous black vitta of the elytra is continuous from the
base to the suture at the summit of the declivity, and there is an
additional brief arcuate vitta on the basal third. The paratype has
the rostrum intermediate in width between the type and allotype; the
setae are more like those of the male.
This species and conquisitus bear the same type locality labels of
Sabanilla, but given the general nature of the labels could, in fact,
be from quite different habitats. Dr. Ohaus (1908:387) briefly
describes his stay in the area at about 1900 m altitude, 4 hours above
Zamora, 2 days' journey from Loja.
The two species are very close, and I interpret the circle of 4
apical lobes on the internal sac of scambus as indicating this to be
114 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
the more derived species.
The word scambus means bow-legged and refers to the strongly bowed
fore tibia, a character readily distinguishing this species from
conquisitus.
45. Hadromeropsis (Hadrorestes) magicus (Pascoe)
Figs. 36, 249-253, 301, 331, 332, 347; Map 12
Naupactus magicus Pascoe, 1881:41:-42. Type, unique female, labelled
"Type, ‘Brazil" on ellipse of pink paper, "Naupactus magicus
Type Pasc," "Pascoe Coll. B.M. 1893. 60° (London).
Hadromerus magicus (Pascoe); Kuschel, 1955:278.
Diagnosis.-Black; elytra smooth and shiny without tubercles except
a few on declivity. Male sharply marked with three conspicuous white
spots on each elytron (Fig. 36), female sharply marked with vittate
pattern. In male elytral interval 10 opposite metasternum much wider
than adjacent interval 9, smooth; in female more nearly equal,
Squamose. Mesepisternum with dense cluster of large white scales.
Description.-Male, length 10.4-10.8 mm, width 3.7 mm. Female,
length 12.3 mm, width 4.8 mm. Mostly glabrous; marked with large,
Shiny white scales as follows. Scattered scales around epistoma.
Male (Figs. 36, 251) elytra with spots on base of interval 4, on
intervals 4-/ just before middle, and on intervals 3-6 at apical
umbone. Female with markings on head and prothorax as in Fig. 249,
elytral markings as in Fig. 252. Female sharply vittate; a vitta on
interval 2 from base to summit of declivity; a vitta from anterior
edge of eye continuing along side of prothorax and continuing on
elytral interval 4 to its apex; this vitta crossing to interval 6 at
basal 0.3 continuing thence in broad vitta, at apical 0.3 gradually
curving to stria 1 at summit of declivity, interrupted only by a round
black spot from striae 5-/ on apical 0.3. Both sexes ventrally with
similar large white scales aggregated on mesepisternum and scattered
on sides of metasternum, and in front of fore and hind coxae. Head
and rostrum punctate, more sparsely so in female; dorso-lateral edges
of rostrum slightly divergent distally, median line finely impressed
between eyes; rostrum moderately concave. Epistoma occupying
approximately 0.4-0.5 of anterior edge of rostrum in male, 0.3 in
female. Mandible with transverse groove shallow, broad, well-defined;
weaker in male. Segment 1 of funicle 0.6-0.8x as long as segment 2.
Prothorax of male 1.06x wider than long, sides moderately to strongly
rounded between constrictions; prothorax of female as in Fig. 249,
1.1x wider than long. Disc of pronotum almost flat in profile, median
line obsoletely impressed; disc of male smooth or with a sculpture of
indistinct punctures and confluent low tubercles, changing to uniform,
low tubercles on sides, each tubercle with slender white decumbent
seta; a few setae more erect on sides of constrictions. Scutellum
densely clothed with white hair-like scales; female with one scale in
addition. Elytra across humeri 1.3x wider than prothorax in male,
1.5x in female; 3.0x longer than prothorax in male, 3./x in female.
In dorsal view sides of elytra of male (Fig. 36) subparallel to middle
thence very gradually rounded to apex; apical umbone very weak and
Howden: Hadromeropsis | 115
just touching outline; apices briefly individually rounded. Elytra of
female wider just caudad of middle, apical umbone as in male;
declivity (Fig. 253) slightly concave between suture and apical
umbone, the transverse apical portion of interval 9 glabrous,
prominent and with a few small tubercles; sutural interval terminating
in tooth. Elytra with sculpture and interval 10 as in Diagnosis and
Figs. 251, 252. Base of elytra not depressed behind scutellum, but
flattened around scutellum in female; base obsoletely depressed at
striae 4 and 5; base with a few short to long, fine, white setae.
Striae regular except obliterated beneath squamose areas, strial
punctures approximately the diameter of a scale; intervals smooth and
polished with an occasional fine puncture. Intervals 9 and 10 with
very fine, moderately long recumbent setae. Fore femur of male
1./-1.8x, of female 1.2x wider than hind femur; distally with weak
serrulate flange; with faint honeycomb microsculpture becoming
rugulose distally, without tubercles; set with very fine, straight
setae. Fore tibia straight to apical fourth whence slightly inwardly
bowed; surface punctate; inner edge with 12 small, uniform teeth.
Middle and hind tibiae cylindrical, with row of bristles and tubercles
of inner edge not strongly developed. Caudal surface of ventrites 2,
3, and 4 of female equal in height; edge of ventrite 2 rounded; edge
of ventrites 3 and 4 acute. Ventrites 3, 4, and 5 basally with
conspicuous honeycombed microsculpture. Ventrite 5 of male with
entire surface with shallow but broad punctures; apex broadly
truncate-emarginate, deflected (Fig. 301). Ventrite 5 of female as in
Fig. 250, across base 1.6x wider than long; apex emarginate. Male
genitalia as in Figs. 331, 332; aedeagus 3.5-3.7 mm long, apex of
internal sac 1.5 mm long. Female genitalia as in Fig. 347;
Spermathecal duct 2.0 mm long.
Distribution.-Map 12. BRAZIL: 1 female (the type), locality
questionable (see Remarks) (London). COLOMBIA: 1 male, no data
(Auckland); 1 male, Bogota (London); 1 male, Fusagasuga, V.18 (Paris).
No data: 1 male (Oxford).
Remarks.-I hesitated to associate these four males with the very
differently marked unique type of magicus for two reasons. First, I
do not believe the species could range from "Brazil" (as the type is
labelled) to Bogota and Fusagasugaé; hence if the association is
correct, the Brazil label is suspect. Secondly, the length of the
apex of the internal sac of the males would seem to suggest a longer
Spermathecal duct. However, other factors seemed to outweigh these
considerations. Especially significant is the squamose mesepisternum
and the elytral spots of the males occurring in positions that are
also squamose in the female.
The white spots of the males are very uniform in all four
Specimens although the scales in one are distinctly oval. The apex of
the internal sac is intermediate in length within the group.
46. Hadromeropsis (Hadrorestes) nitidus n. sp.
Figs. 239-242, 300, 333, 334, 348; Map 12
Diagnosis.-Based on unique male. Shiny black, sparsely clothed
116 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
with small, round, bright blue scales. Elytra convex in cross
section. Last tergite narrow apically. Sclerotized apex of internal
sac tubular, 2.4 mm long, stiff.
Description.-Holotype, male, length 11.4 mm, width 3.9 mm. Color
as in Diagnosis. Scales of elytra set in brief, shallow transverse
depressions or on the smooth surface. Head and rostrum sparsely
punctate (Figs. 239, 242). Dorso-lateral edges of rostrum slightly
divergent apically, high, surface deeply concave between; median line
impressed between anterior half of eyes, a few brief impressed lines
parallel to it. Epistoma (Fig. 242) occupying 0.4 of anterior edge of
rostrum, as long as wide, sides almost parallel, apex broadly rounded.
Mandible with weak transverse groove, its anterior edge being the edge
of scar of cusp. Funicle with second segment 1.2x longer than segment
1. Prothorax (Fig. 239) 1.1x wider than long, sides strongly rounded
between constrictions; disc gently arcuate in profile. Pronotum with
median line unmarked; basal constriction smooth and polished with
trace of impressed lines on right side; sculptured with uniform, low,
round tubercles which are contiguous on sides, some confluent on disc;
setae arising from tubercles very inconspicuous, as long as diameter
of a tubercle, recumbent. Scutellum with very fine recumbent setae,
no scales. Elytra across humeri 1.3x wider than prothorax, 3.2x longer
than prothorax, 2.3x longer than width across humeri. In dorsal view
sides of elytra parallel for basal half thence very’ gradually
convergent to apex (Fig. 241), weak apical umbone just touching the
Outline; apex rounded, its edge conspicuously dentate. In dorsal
Outline, a few very weak tubercles on sides of elytra on basal fourth
and apical half. Elytra transversely convex. Base of elytra with
Stria 5 weakly depressed, postscutellar depression obsolete; base of
elytra with a few very fine, dark, moderately long, erect setae. Disc
of elytra with no tubercles from base to apical fourth where weak ones
appear in intervals and striae, those of declivity small but more
acute. Striae 9 and 10 opposite metasternum (Fig. 240) not more
widely separated than striae 8 and 9. Intervals 9 and 10 with no
erect setae. Fore femur 2.0x wider than hind femur; distal flange
weak, edge granulate; anterior and posterior face smooth and shiny
proximally, distally with weak honeycomb sculpture rapidly changing to
impressed lines, with no shelf-like tubercles on posterior face; set
with fine, stiff, dark setae. Fore tibia straight until distal third
whence moderately inwardly bowed; inner edge with 11 small teeth and
distal half with multiple long, dark, stiff setae; surface punctate,
more coarsely so on outer surface. Dorsal surface of tarsi clothed
with prostrate pale blue seta-like scales and conspicuous, stiff,
distally-directed black bristles. Middle and hind tibiae on inner
edge with row of 4 or 5. stout bristles, without tubercles.
Mesepisternum moderately convex and with brief row of blue scales on
Outer edge. Metasternum and abdomen smooth and polished with numerous
very fine, erect setae. Ventrite 5 (Fig. 300) with a few very fine
punctures; apex broadly, deeply emarginate. Last tergite as in
Diagnosis. Genitalia as in Figs. 333, 334. Aedeagus 3.6 mm long;
internal sac with conical apex elongated into tube exteriorly minutely
Spiculate on basal half, more than 2.4 mm long (extreme apex
accidentally broken off).
Type Series.-Holotype, ECUADOR, Napo, 7 km S Baeza, 22 Feb. 1979,
Howden: Hadromeropsis 117
H & A Howden, walking up blade of grass (Howden).
Remarks.-There is a female labelled "Columbia Baden" in the
Dresden collection which I tentatively assign to this species. It
differs from the type as follows. Length 12.3 mm, width 4.5 mm. All
scales larger, very pale green except those forming a pattern on
elytra dense, whitish; pattern consisting of a long loop from base of
stria 4 to stria 2 at apical third and back to beneath humerus, a
second oblique elliptical mark outlining apical umbone. Head, rostrum
and prothorax similar to male except segment 1 of funicle slightly
longer than segment 2. Elytra more coarsely sculptured and flatter;
elytra 3.6x longer than prothorax; sutural interval at apex not longer
than denticles along margin; striae 9 and 10 more widely separated
Opposite metasternum. Caudal surfaces of ventrites 2, 3, and 4
perpendicular, equal, moderate; ventrite 5 without’ lateral
depressions; apex narrowly, deeply notched. Genitalia as in Fig. 348;
spermathecal duct 5.0 mm, extreme in length as is the male endophallic
structure.
The type of magicus resembles this female but differs in segment 2
of the funicle longer than 1; elytra with straight white vitta on
interval 2 and vitta of stria 4 straight-edged until declivity, thus
leaving intervals 1, 3, and most of 4 bare until declivity.
The mealy substance of Fig. 239 is incompletely dissolved wax;
Fig. 240 shows large areas of untouched wax.
The type of nitidus resembles spiculatus in habitus but nitidus
has the sides of the prothorax rounded instead of almost
parallel-sided, disc of pronotum not flattened broadly, last tergite
narrow, fore femur with setae of posterior face arising from almost
smooth surface, elytra narrower apically, internal sac different and
terminal tube spiculate proximally only and more slender.
All the definitions of the Latin adjective "nitidus" are
appropriate for this species: shining, sleek, in good condition,
elegant, etc.
47. Hadromeropsis (Hadrorestes) mandibularis n. sp.
Figs. 243-248, 346; Map 13
Diagnosis.-Mandible with two stout dorsal setae set in deep,
Sharply defined transverse groove (Fig. 243). Without full-sized
scales dorsally or ventrally. Disc of prothorax with punctures in
female or irregular pustules in male which gradually change to low,
rounded tubercles on sides; median line unmarked. Apices of elytra of
male broadly, individually rounded (Fig. 247). Fore femur of males
sculptured as in Fig. 246. Spermathecal duct 4.5 mm long.
Description.-Holotype, female, length 16.2 mm, width 6.0 mm.
Black; legs and antenna piceous. Clothed with minute greenish white
scales; scales sparse on rostrum, head and prothorax, aggregated in
transverse depressions on disc of elytra, more numerous on declivity.
Head and rostrum (Fig. 243) uniformly punctate. Median line impressed
for short distance on rostrum to between middle of eyes, with a few
parallel grooves either’ side. Rostrum only slightly concave.
Epistoma as in Fig. 243, 244; mandible as in Diagnosis and Fig. 244.
118 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Funicle with segments 1 and 2 approximately equal in length. Head
robust, eyes not very prominent. Pronotum as in Diagnosis and Fig.
245. Prothorax 1.09x wider than long, sides gently rounded between
weak constrictions, widest before middle; anterior constriction
unmarked on disc, basal constriction very weak; setae arising from
lateral tubercles fine, recumbent, about as long as diameter of a
tubercle. Scutellum with whitish seta-like scales. Elytra across
humeri 1.6x wider than prothorax, 3.8x longer than prothorax. In
dorsal view, sides almost parallel, very slightly convergent from
about middle, apical umbone slightly arcuate in outline, sides thence
almost straight to apex. In dorsal outline no tubercles present
except small ones on apical umbone; margin of elytra conspicuously
dentate around ventrite 5, sutural interval not modified into tooth.
Elytra in profile flattened behind scutellum for basal seventh, then
abruptly deflected, flat to summit of declivity, suture here set with
or 8 stout dark setae. Base of elytra with stria 5 scarcely
depressed, without long setae. Intervals 1, 2, and 3 flat, smooth and
polished, without squamose transverse depressions from near base
almost to declivity in an elongate V. Elytra without tubercles except
on declivity and just before apical umbone (Fig. 248); striae very
regular; interval 10 wider opposite metasternum, interval 9 wider from
hind coxa to apical umbone. Fore femur 1.5x wider than hind femur,
with a weak serrulate flange; fore tibia with 10 small equal teeth on
inner edge; outer edge punctate and set with numerous long, dark, wiry
setae. Inner edge of middie tibia with row of 8 stout bristles each
set at base of a sharp tubercle, hind tibia with 4 or 5 such bristles
without tubercles. Caudal surface of ventrites 2 and 3 moderate,
anteriorly slanted, equally high, edge not at all acute. Caudal
surface of ventrite 4 less slanted, edge acute. Ventrite 5 across
base 1.6x wider than long, feebly convex medially; apex narrowly
truncate. Genitalia as in Fig. 346; spermathecal duct 4.5 mm long.
Allotype, male, length 11.6 mm, width 4.0 mm. Complete
description impossible because of condition of specimen which is
partly destroyed by dermestids, missing antennae except right scape
and entire abdomen except ventrites 1 and 2. Differs from type as
follows. Scales less numerous. Rostrum with median line sharply
impressed between eyes only, entire rostrum concave, longitudinally
convex either side of median line, the longitudinal grooves of the
type represented by 2 traces. Transverse groove of mandible less
developed. Pronotum more coarsely sculptured, punctures more or less
replaced by irregular low pustules. Elytra across humeri 1.3x wider
than prothorax, 3.0x longer than prothorax. Sides of elytra parallel,
very gradually convergent from about 0.6, umbone weak, just touching
dorsal outline; apices (Fig. 247) broadly, individually rounded. In
dorsal outline, tubercles of lateral intervals obsolete basally,
absent medially, conspicuous apically, denticles of apical edge very
conspicuous. Smooth, polished area of intervals 1, 2, and 3 reduced
to basal 0.5. Fore femur 1.8x wider than hind femur; sculpture as in
Fig. 246; without shelf-like tubercles on posterior face. Fore tibia
Straight until basal 0.25 whence slightly curved inward. Middle and
hind tibiae with bristles scarcely thicker than other setae, tubercles
replaced by granules. Abdomen missing.
Type Series.-Holotype, COLOMBIA, S. Antonio, ex. coll. Clerc
Howden: Hadromeropsis 119
(Paris). Allotype, COLOMBIA, St. Antonio, 2000 m, 16.6.1908, Coll.
Pape, Hust. det., Hadromerus prope scabricollis Fst (Eberswalde).
The type locality could be the San Antonio on the road between
Cali and Buenaventura where Fass] collected (Voss, 1953:29).
Remarks.-Bearing strong resemblance to nitidus and magicus in the
head and rostrum and sharing the strong mandibular groove with
cavifrons and magicus, mandibularis can be distinguished by the
diagnostic characters. From cavifrons it also differs in the simpler
rostrum and lack of tubercles on elytral intervals 8 and 9. A
mandibular groove is also present in the impressicollis and alacer
groups.
The very long spermathecal duct (second in length only to that of
nitidus? female) suggests that the male will be found to have a very
long endophallic structure, slightly shorter than that of nitidus,
longer than that of magicus.
H. mandibularis 7s most closely related to nitidus, the males of
these two species being most readily distinguishable by the shape of
the elytra which in nitidus are more convex in cross section and
profile, more nearly vertical at apex, more narrowly rounded at apex,
and with weaker postscutellar depression. When more specimens are
found, it is probable that additional characters will be found in the
ventrite 5 and last tergite as well as in the genitalia.
The name mandibularis refers to the extreme development of the
dorsal groove on the mandible.
48. Hadromeropsis (Hadrorestes) spiculatus n. sp.
Figs. 38, 280, 286-288, 327, 357; Map 12
Diagnosis.-Resembling pectinatus, differing especially in the
following. Slender in habitus (Fig. 38). Pronotum flattened medially
(Fig. 288). Apical edge of elytra of female briefly indented before
sutural tooth (Fig. 280). Fore tibial teeth more uniform in size and
anterior face of fore tibia punctate only. Internal sac as in Fig.
327, apex spiculate, very long.
Description.-Holotype, male, length 10.8 mm, width 3.6 mm.
Piceous, except head, base of rostrum and most of prothorax black.
Head and rostrum (Fig. 288) similar to pectinatus but sculpture finer,
fovea absent and median line finely impressed to behind eyes. Funicle
with segment 2 subequal to segment 1. Prothorax (Fig. 288) scarcely
wider than long, sides only weakly rounded between constrictions;
prothoracic sculpture consisting of low rounded tubercles of
approximately uniform diameter, tubercles of broad median flattened
area very shallow and tending to be arranged in rows; setae of
prothorax long, more slender than in pectinatus. Elytra across humeri
1.2x wider than prothorax; elytra 3.1x longer than prothorax, 2.4x
longer than width across humeri. In dorsal view (Fig. 38) sides of
elytra parallel for basal 0.2, thence very slightly wider, tapering
gradually to apex from apical 0.5, apical umbone very weak but
touching outline. Base of elytra depressed at stria 5, more strongly
depressed behind scutellum than in pectinatus. Elytral tubercles less
developed than in pectinatus, absent on sides of elytra centrally.
120 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Elytral surface smooth and polished between striae with no sculpture
except that of declivity which gradually begins caudad of middle;
striae very regular and distinct on disc, still recognizable on
declivity. Fore femur 2.4x wider than hind femur. Entire surface of
fore femur with fine microsculpture, on anterior face (Fig. 286)
rugulose, on posterior face (Fig. 287) finely impressed netted or
honeycomb sculpture, distal half with superimposed crowded large
setiferous tubercles not strongly shelf-like; inner edge distally with
gradual, weak flange, sharply denticulate on edge. Fore tibia (Fig.
286) with sculpture of punctures only, with 8-10 sharp teeth on inner
edge and a few extra granules on posterior face. Middle tibia on
inner face near edge with 3-5 sharp tubercles each with a stout
bristle; hind tibia with 3 bristles without tubercles. Genitalia as
in Fig. 32/7; aedeagus 3.5 mm; internal sac with apex elongated into
stout exteriorly spiculate tube 2.5 mm long.
Allotype, female, length 13.1 mm, width 5.0 mm. Differs from type
as follows. Reddish-brown (slightly teneral), only meso- and
metasterna, scutellum, head and base of rostrum black. Normal
vestiture uncertain because of teneral condition, but elytra with many
minute elongate scales and with full-sized creamy white scales (mostly
transparent in allotype) forming a vitta on left elytron from humerus
on interval 7 to interval 5 at middle. Rostrum wider, more densely
sculptured. Elytra across humeri 1.5x wider than prothorax; elytra
3.5x longer than prothorax; elytra 2.4x longer than width across
humeri. Elytra slightly wider at middle, apex more elongate (Fig.
280). Sutural interval at summit of declivity with 15-16 long, erect
setae. Fore femur 1.4x wider than hind femur, sculpture as in type
but without shelf-like tubercles; flange of inner edge and denticles
scarcely weaker than in type. Middle tibia without tubercles on inner
face, with 6 or 7 stout bristles; hind tibia with 3 stout bristles.
Caudal surface of ventrites 2 and 3 anteriorly inclined, edge not
sharp; smooth and shiny but with trace of sculpture basally. Caudal
surface of ventrite 4 perpendicular, edge straight in posterior view,
smooth and polished. Ventrite 5 across base 1.5x wider than long,
only feebly convex medially. Genitalia very extreme in development
(Fig. 357), spermathecal duct of average diameter at nodulus only,
gradually becoming larger and testaceous in color, expanded and
bulbous before bursa, narrower again at entrance of bursa.
Type Series.-Holotype, PERU, Huanuco, Acomayo, 2100 m, 7 June
1946, F. Woytkowski Coll., Donor Wm Proctor (New York). Allotype,
PERU, Huanuco, Carpish, 2800 m, 14 Oct. 1946, F. Woytkowski Coll.,
Donor Wm Proctor (New York). Paratype, 1 female, BOLIVIA, L. P., 9 mi
NE Unduavi, Chuspipata Ridge, cloud forest, Apr. 9, 1979, Collectors:
L &C.W.O'Brien (0 Brien). 7
Remarks.-The paratype is 11.3 mm in length, 4.2 mm in width. Like
the allotype it also appears slightly teneral, but the vestiture is in
fresh (not waxy) condition and the dorsum bears a few more scales.
The paratype differs as_ follows. Rostrum, prothorax, elytra,
appendages reddish-brown; head, meso- and metasterna and abdomen
black. With minute elongate white scales scattered on dorsum of head
and rostrum, sides and disc of prothorax, and elytra except medially;
a glabrous area on elytra vaguely outlined by larger scales from
interval 4 and 5 at base to suture at apical 0.25. Long, conspicuous,
Howden: Hadromeropsis 121
fine white setae on sides of prothorax and sides of rostrum apically.
Elytra 4.1x longer than prothorax, base of elytra scarcely impressed
at interval 5. Most setae abraded from sutural interval at summit of
declivity. Fore femur 1.2x wider than hind femur. Ventrite 5
moderately convex on apical half. Spermathecal duct "normal", i.e.,
not distended as in allotype; 1.7 mm long.
The difference in the spermathecal duct between the allotype and
paratype seems too great for intraspecific variation. Is =the
difference attributable to some physiological factor, or age, or are
two species involved?
The species is named spiculatus because of the extreme spiculate
apex of the internal sac.
Species Not Assigned to Group
49. picchuensis n. sp. 50. cavifrons n. sp.
| Remarks.-Based on the small sample (four specimens) of females
only, the relationships of these two species are not obvious, but they
do belong to Hadrorestes.
49. Hadromeropsis (Hadrorestes) picchuensis n. sp.
Figs. 31, 271-273, 353; Map 12
Diagnosis.-Based on female only. Clothed with round, mostly
discrete scales of cream, pale tan or rose, at most only faintly
iridescent; elytra with larger white scales arranged in faint fasciae
and vaguely outlining common glabrous area on basal half medially as
in Fig. 31. Disc of pronotum broadly flattened (Fig. 271). Elytral
intervals 8, 9, and 10 with very long setae set at a 45° angle or
greater, setae very conspicuous in dorsal view. Genitalia with a
large sclerite in bursa copulatrix at junction of duct (Fig. 353).
Description.-Holotype, female, length 10.5 mm, width 4.3 mm.
Integument brown, head and rostrum piceous except part of mandible and
epistoma reddish. Squamose as in Diagnosis, Fig. 31. Rostrum with
dorso-lateral edges parallel, sides almost perpendicular, surface of
rostrum almost flat (flatter than in Fig. 271 of paratype); median
line briefly impressed between eyes; with a few fine, glabrous rugulae
showing between scales of head and rostrum. Mandible with one long
dorsal seta set in a vague shallow depression. Funicle with segments
1 and 2 subequal. Prothorax as in Diagnosis and Fig. 271; 1.2x wider
than long, sides moderately rounded between weak constrictions. Sides
of prothorax with scattered weak tubercles only slightly larger than a
scale, each tubercle bearing a very fine seta as long as 2-3 scales,
setae closely appressed. Prosternum with scales’ transversely
elongate; with long, wispy setae. Scutellum densely clothed with
imbricate scales. Elytra as in Diagnosis and Fig. 31. Elytra across
humeri 1.4x wider than across prothorax; 3.7x longer than prothorax.
In dorsal view sides of elytra slightly divergent from humeri to just
beyond middle, thence gradually converging to apex; apical umbone
weak, feeble in dorsal outline; a few weak setiferous tubercles
122 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
present in dorsal outline basally and apically. Elytra in profile
with declivity very gradual, summit unmarked except by 7 or 8 long,
wispy setae; sides of elytra strongly turned under opposite ventrites
2, 3, and 4 (Fig. 273) (partly an artifact of teneral condition?).
Base of elytra obsoletely depressed at stria 5, distinctly depressed
behind scutellum; base of elytra with many long, wispy setae, some as
long as the long setae of summit of declivity; some setae arising from
tubercles like those of prothorax; similar tubercles present on apical
third of elytra including declivity. Striae almost completely
regularly punctate. Apex of elytra as in Fig. 272; edge with
scattered denticles smaller than an adjacent scale; sutural interval
attenuate into small tooth. Fore femur 1.2x wider than hind femur,
distal flange obsolete; faint sculpture concealed by scales. Fore
tibia straight, inner edge with 8-10 acute teeth, each tooth with an
unusually conspicuous bristle exceeding the tooth in length (an
artifact of teneral condition?). Middle tibia with 5, hind tibia with
3 stout bristles on inner surface dorsally. Abdomen crumpled in type,
apparently similar to that of paratype which has caudal surface of
ventrites 2, 3, and 4 perpendicular, moderate, equal. Ventrite 5
almost flat, no lateral depressions, median convexity very weak, 1.6x
wider than long. Genitalia as in Fig. 353; spermatheca very slender,
in one plane; spermathecal duct 2.5 mm long, with a large sclerite in
bursa at junction of duct.
Type Series.-Holotype, PERU, Cuzco, Torentoy Canyon (Base Machu
eon 2000 m, VI-VII.1964, B. Malkin (So Paulo). Paratype, 1
female, PERU, Cuzco, Machu-Picchu (sobre ruinas, 2600-2800 Mm),
1-2.VI1.1964, B. Malkin (Howden).
Remarks.-The paratype appears to be slightly more teneral than the
type and was not dissected. It measures 9.5 mm long, 3.9 mm wide, and
differs conspicuously only in the apex of the elytra which has the
tooth almost absent. yar
The pattern formed by. the scales, the softer integument (although
possibly only an artifact of teneral condition), and the spermatheca
in one plane are characters more common in the nominate subgenus. The
large bursal sclerite is similar to that of the argentinensis and
nobilitatus groups, but the sclerotized streaks of the vagina of those
groups are_ absent. The lateral sclerites are exclusive’ to
Hadrorestes. Characteristics of the male genitalia are difficult to
predict.
50. Hadromeropsis (Hadrorestes) cavifrons n. sp.
Figs. 282-285, 356: Map 13
Diagnosis.-Based on female only. Frons and rostrum grossly
hollowed out, the dorso-lateral edges of rostrum elevated, thus
accentuating the concavity (Figs. 282, 283). Mandible with dorsal
setae set in a deep transverse groove. Elytra with sharply defined
markings of yellowish scales forming a basal ring, median zigzag
fascia and an apical band or ellipse encircling apical umbone.
Spermathecal duct 2.5-3.0 mm long.
Description.-Holotype, female, length 17.4 mm, width 6.8 mm.
Howden: Hadromeropsis base
Black; femora and tibiae pale reddish, black at ends. Integument
dorsally and ventrally apparently with sparse, minute, green scales
which are mostly abraded; prothorax and elytra with a pattern formed
by large yellowish, dense scales; on prothorax (partly abraded) in at
least a line anteriorad of basal constriction continuing ventrad
beside and behind fore coxa. Elytral pattern consisting of basal ring
between stria 5 and scutellum; thick median zigzag fascia; and broad,
oblique ellipse just before declivity. Hind coxa covered with green
and yellow scales of various shapes, medium size. Head and rostrum as
in Diagnosis and Figs. 282, 283. Segment 2 of funicle slightly but
distinctly longer than segment 1. Prothorax (Fig. 283) with disc
almost smooth, median line obsoletely finely impressed; sides very
weakly tuberculate. In profile almost flat, except for elevated basal
constriction. Scutellum with a few small, round, green scales.
Elytra across humeri 1.6x wider than prothorax, 3./x longer than
prothorax, 2.3x longer than width across humeri. In dorsal view sides
rounded at about middle, the gentle curve continuous with apical
umbone; sides of apex weakly curved from beneath stria 4 to suture,
its edge strongly dentate, sutural interval elongated into a very
brief tooth (Fig. 285). Base of elytra with very weak postscutellar
depression, humeri suddenly produced from stria 5. Sides of elytra in
dorsal view with continuous small, acute tubercles, tubercles situated
on intervals 8 and 9. Interval 10 opposite metasternum wide,
tuberculate; striae here and on declivity somewhat irregular,
elsewhere regular. Suture at summit of declivity with 8 long, dark
setae. Fore femur 1.3x wider than hind femur, with weak serrulate
flange. Fore tibia with 14-16 very small teeth on inner edge; outer
edge of fore tibia with long setae not stiff and wiry; outer surface
punctate, some punctures coalescing into short grooves. Middle tibia
on outer edge with 2 sulci, inner surface with row of 10 stout
bristles. Hind tibia (Fig. 284) on outer edge with single sulcus;
inner surface with row of / stout bristles. Caudal surface of
ventrites 2, 3, and 4 slightly overhanging succeeding ventrites,
equal, sharp-edged. Ventrite 5 with moderate median convexity; across
base 1.4x wider than long; apex narrowly rounded. Genitalia as in
Fig. 356; without lateral sclerites, no sclerite seen at junction of
duct with bursa copulatrix; duct 2.5 mm long, testaceous. Spermatheca
strongly twisted in several planes.
Type Series.-Holotype, PERU, Piches and Perenes Vs, 2000-3000 ft,
Soc. Bao de Lima (Washington, USNM Type No. 100192). Paratype, 1
female, PERU, Hudnuco, Divisoria, 1600 m, 31.7.47, Schunke leg., coll.
Kuschel (Auckland).
Remarks.-The paratype is 15.8 mm long, 6.0 mm wide, and differs
from the type as follows. Elytral median fascia on side of elytra at
stria 7 continues anteriorly in a vitta to base of interval 9; elytra
across humeri 1.5x wider than prothorax; elytra 3.8x longer than
prothorax; sides of elytra in dorsal view with no tubercles in central
portion; fore femur 1.5x wider than hind femur; middle and hind tibiae
with only 4 stout bristles each; all tibiae without sulci on outer
surface; caudal surface of ventrites 2 and 3 not overhanging but
slightly anteriorly slanted; ventrite 5 across base 1.6x wider than
long; spermathecal duct 3.0 mm long ending in a large disc inside
bursa copulatrix. The significant differences are the presence of a
124 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
bursal sclerite and the smooth, non-sulcate tibiae. Since I am
certain the two females are conspecific, then the bursal sclerite and
sculpture of the tibiae must be added to the long list of
intraspecifically variable characters.
Because this species clearly belongs to Hadrorestes in all the
Characters listed for the subgenus except for the lack of paired
lateral sclerites, I presume these have been secondarily lost. More
material, especially males, are needed to establish the relationship
of this species to others.
Incertae sedis
51. Hadromeropsis earinus n. sp. 92. Hadromeropsis striatus n. sp.
These two species, each described from a unique specimen, are not
assigned to a subgenus for the reasons discussed under Remarks.
o1. Hadromeropsis earinus n. sp.
Figs. 289-293, 335
Diagnosis.-Based on unique female. Eye small (Fig. 289),
separated from prothorax by its length. Clothed with iridescent
scintillating green scales. Prothorax (Fig. 290) with basal and
apical constrictions strong laterally and dorsally, surface
irregularly sculptured and subtuberculate on sides. Base of elytra
between striae 5 abruptly perpendicular and slightly anteriorly
produced. Margin of caudal surface of ventrites 2, 3, and 4 not
acute, the edge and half the adjacent caudal surface densely covered
with elongate appressed scales (Fig. 293). Spermatheca with ramus
replaced by circular membranous area. With neither sclerites in the
bursa copulatrix nor lateral sclerites in the vagina.
pescript ion, Holotype: female, length 13.0 mm, width 4.6 mn.
Black. Clothed as in Diagnosis. Scales small, circular; dense,
imbricate ventrally; less dense on dorsal surface, elytra appearing
slightly tessellate because of varying density of scales. Dorsal
setae short, broadly lanceolate to almost spatulate, curved, as long
as 1-2 scales. Head and rostrum as in Fig. 289. Rostrum 1.26x longer
than width at apex, strongly longitudinally concave from between eyes
to about middle, dorso-lateral edges prominent, apically divergent;
median line finely impressed between apical half of eyes. Surface of
head and rostrum not sculptured. Mandible without dorsal groove, with
only one long seta arising from a fovea. Funicle with segments 1 and
2 equal in length; antennal club very long, as long as segments 1 to 4
of funicle. Prothorax as in Fig. 290, Diagnosis; 1.08x wider than
long. Postocular vibrissae very well developed, reaching 0.6 to eye.
Scutellum small, squamose as elytra, broadly rounded posteriorly.
Elytra across humeri 1.5x wider than prothorax, elytra 3.8x longer
than prothorax; elytra 2.4x longer than width across humeri. In
dorsal view base of elytra (Fig. 290) slightly arcuately emarginate
between striae 5 and as in Diagnosis; humeri_ strongly angled
Howden: Hadromeropsis 125
posteriorly, sides of elytra gradually divergent to middle where they
are 1.15x wider than across humeri, thence gradually converging to
elongate apex, apical umbone briefly entering outline. Sides of apex
straight caudad of umbone, apex (Fig. 291) elongate, suture attenuated
into conspicuous tooth approximately 0.5 mm long. Lateral edge of
elytra absolutely smooth. Elytra nowhere with tubercles; with strong,
transverse postscutellar depression; interval 7 faintly keeled between
middle and apical umbone; umbone slightly keeled, this keel continuing
obliquely towards apical tooth (Fig. 291). Remainder of surface very
faintly, irregularly, undulating and faintly depressed around
punctures. Suture at summit of declivity with approximately 15 very
conspicuous, long, straight, white setae. Striae regularly punctate;
each puncture approximately as wide as a scale, each with a broad seta
curled over it; striae 9 and 10 concealed by densely imbricate scales,
but traceable by setae, clearly visible from inside elytra. Legs
without sculpture. Fore femur slender, 1.08x wider than hind femur,
1.2x wider than middie femur; with no trace of flange on inner edge
distally. Fore tibia long, slender, distal 0.3 bowed inward; inner
edge with 13 small, equidistant teeth, the oblique bristle on distal
face of each tooth longer than tooth. Middle tibia on inner face with
9 strongly oblique bristles, most set on small tubercles; hind tibia
with 6 oblique bristles without tubercles. Suture between ventrites 1
and 2 strongly anteriorly arcuate on central half (Fig. 292). Caudal
margin of ventrites 2, 3, and 4 as in Diagnosis and Fig. 293.
Ventrite 5 across base 1.4x wider than long, with a slight convexity
on either side near base, moderate median convexity, apex narrowly
truncate. Genitalia as in Diagnosis and Fig. 335, spermatheca in one
plane, spermathecal duct approximately 1.4 mm long.
Type Series.-Holotype, ECUADOR, - -Lillegible], Coll. J. Faust,
Ankauf 1900 (Dresden). |
Remarks.-Some of the characteristics of this unique female are so
extreme that its relationship to other species groups is obscure. the
partially squamose and rounded edge of the caudal margin of ventrites
2, 3, and 4 are the most extreme in the genus, but a glabrous male of
this species might have no scales and the edge acute. The suture
between ventrites 1 and 2 is much more strongly arcuate than in any
Hadromeropsis seen. The fore femur is slightly more slender than in
any other female seen. The membranous ramus is unique and so unusual
that one might suspect an aberration. I take a conservative position
here and wait for more material to clarify the situation.
When a male of this species is available, subgeneric placement can
be reconsidered on the condition of its vestiture, including the
caudal margin of ventrites 2, 3, and 4; the edge of the elytra (males
of Hadrorestes often have the denticles of the edge of the elytra
stronger than in the female); and the form of the endophallic
structure. |
The habitus of earinus is more like that of Hadrorestes than the
nominate subgenus, but it does not fit there because the edge of the
elytra is smooth, striae 9 and 10 are well-separated their full
length, the striae are regular beneath the apical umbone, and there
are no lateral sclerites in the vagina. Of the species groups,
earinus seems most closely related to the alacer group which has the
eye distant from the prothorax, scarcely enlarged fore femur in the
126 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
female and less acute caudal margin of ventrites 2 and 3. It differs
from that group in the strong postocular vibrissae, regularly aligned
strial punctures, strongly depressed postscutellar area, and segments
1 and 2 of funicle equal.
The name is derived from the Greek word "“earinos" meaning the
color of spring green.
92. Hadromeropsis striatus n. sp.
Figs. 358-362, 368-370
Diagnosis.-Based on unique male. Rostrum narrow in dorsal view,
thin in profile (Figs. 358, 359). Elytra with prominent, straight
Striae; strial punctures deep; intervals convex. Brachypterous: wing
0.6x length of elytron, mesepimeron narrow, elytra extremely narrow
across humeri. Fore femur enormously swollen; without shelf-like
tubercles on posterior face; with strong flange on inner’ edge
distally. Internal sac (Figs. 368, 369) without internal sclerites;
with heavily sclerotized distal tube.
Description.-Holotype, male, length 11.8 mm, width 4.0 mm. Black
except antennae reddish; with minute blue scales scattered over dorsum
and legs, scales round, oval or elongate. Side of head below eye with
patch of white to gray-blue scales of various sizes and shapes. Head
and rostrum as in Diagnosis, Figs. 358, 359. Dorsum of rostrum very
shallowly concave. Surface of head and rostrum including epistoma and
mandible with fine microsculpture; head and rostrum also with
additional moderate, irregular sculpture, not distinctly punctate;
frontal fovea moderate, median line not marked except as vague carina
from interantennal line to apex of epistoma. Epistoma occupying 0.4
of anterior edge of rostrum, posterior margin thickened. Scrobe more
distant from eye than is usual for genus (Fig. 359). Mandible with no
long dorsal setae, but one moderately long dorso-lateral seta in an
elongate fovea. Antennal scape in resting position reaching anterior
margin of prothorax (Fig. 359, but head twisted in photo) funicle with
segment 1 slightly longer than segment 2. Eye separated from anterior
margin of prothorax by 0./x its own diameter. Prothorax as in Fig.
359. Prothorax 1.1x wider than long; sides in dorsal view almost
Straight, distinctly wider before middle. Surface slightly uneven;
surface evenly, densely covered with slightly irregular rounded
tubercles; each tubercle with a very slender seta, those on sides much
longer and more nearly erect than dorsal setae. Postocular vibrissae
weak. Elytra across humeri only 1.05x wider than prothorax. Elytra
2.3X longer than width across humeri; elytra 2.9x longer’ than
prothorax. Elytra as in Diagnosis. Sides of elytra parallel for
basal 0.26, thence gradually divergent, widest just caudad of middle,
convergent to apex; apex (Fig. 360) truncate from approximately stria
3, sutural interval briefly produced into a tooth. Striae and
intervals very regular, straight; strial punctures very deep and
intervals convex (Fig. 361) from base to unmarked declivity; on
declivity (Fig. 360) strial punctures rapidly becoming obsolete and
intervals flat; small tubercles on basal 0.25 of elytra only. All
surfaces of elytra with irregular microsculpture, more pronounced
Howden: Hadromeropsis 127
laterally and on declivity. Edge of elytra absolutely smooth.
Apparently without long, wispy setae; all intervals with row of pale,
slender setae, those of alternate intervals very slightly longer than
seta of even-numbered intervals; setae suddenly longer, straight and
erect on apical half of elytra laterally and on declivity, the longest
approximately 0.5 mm. Wing as in Diagnosis. Fore femur as in
Diagnosis and Fig. 359, 2.2x wider than hind femur. Surface of fore
femur almost smooth proximally, becoming minutely rugulose distally,
without punctures; inner edge with small scattered tubercles,
tubercles pronounced on distal flange. Fore tibia (Fig. 362) straight
medially, weakly bowed distally and proximally; inner edge very
irregular, proximal half with small tubercles, distal half with large
medial tooth followed by 4 or 5 teeth of various sizes, one bifid on
right tibia of type; fore tibia with numerous granules on anterior and
posterior face, outer edge with small punctures on smooth surface.
Fore tarsus similar to that of pectinatus in Fig. 308. Middle and
hind femora slender for proximal half then abruptly swollen; middle
tibia on inner edge with 5 small indistinct tubercles, larger
tubercles with a stout bristle arising from base; hind tibia without
tubercles or teeth on inner edge. Ventrites 1, 2, and 3 with very
fine microsculpture of transverse rugulae; ventrites 1 and 2 with
setae arising from minute punctures, punctures stronger on ventrite 3.
Ventrite 4 with punctures more numerous. Ventrite 5 (Fig. 370) 1.9x
wider than long; with crowded punctate-rugulose sculpture; sharp
lateral edge stops abruptly at middle of sides, at which point
ventrite becomes convex; apex emarginate. Genitalia as in Figs. 368,
369; aedeagus 3.9 mm, aedeagal apodeme 2.5 mm, tegminal strut 2.6 mm.
Internal sac without internal sclerites; with heavily sclerotized,
stout distal tube.
Type Series.-Holotype, COLOMBIA, Paso Bella Vista above Duria-
maina, 3760 m, 7 Dec. 1978, H. Sturm, in dead leaves of Libanothamnus,
78, coll. Kuschel (Auckland).
Remarks.-The integument of the type was cleaned of a thin film of
transparent wax even though the long, wispy setae usually associated
with wax were not evident.
This species is tentatively assigned to Hadromeropsis because it
shares more characters with that genus than with any other genus I
know. The species does not conform to either of the two subgenera of
Hadromeropsis. Most important, the unique internal sac lacks the
heavy internal sclerites characteristic of all Hadrorestes and of the
argentinensis and nobilitatus groups of the nominate subgenus, but is
not closely related to the remaining flagellate groups either. The
long sclerotized tube at the apex of the internal sac is difficult to
relate to any Hadromeropsis I have seen and a polyphyletic element may
have been introduced by including the species. However, it is
conceivable that the distal fraction of the sclerotized tube
represents the sclerotized apex of Hadrorestes and the long proximal
portion represents the heavy internal sclerites of Hadrorestes without
the membranous case.
Other extreme expression of generic characters are: posterior
margin of epistoma thickened, antennal scape reaching anterior margin
Of prothorax (but almost as long in pectinatus), antennal scrobe well
separated from eye, prothorax with anterior constriction distinct in
128 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
rofile.
: The species resembles a Hadrorestes on external characters but
differs from that subgenus in the well-separated striae 9 and 10 and
the lack of denticles or tubercles around the edge of the elytra. It
is possible though, that both of these qualities are a consequence of
brachyptery, especially in this species with the shortest wing of the
three brachypterous species.
The species is named striatus for the very conspicuous elytral
striae.
ACKNOWLEDGMENTS
Because the genus Hadromeropsis is not well represented in
collections, each of the 31 institutional collections and four
personal collections studied was unique and vital. The institutions
and people responsible for loans of specimens are all thanked for
their valuable contributions.
A seven-week study in Argentina was greatly enhanced by the many
kindnesses of Antonio and Juana Martinez and by the assistance of the
Instituto de Investigaciones Entomologicas Salta (INESALT) in Rosario
de Lerma through M. and J. Viana and G. Williner. Patricia Hoc,
Universidad Nacional de Buenos Aires, kindly identified the food
plants of Curculionidae collected in Argentina.
David Maddison, University of Alberta, painted the habitus of
Hadromeropsis nobilitatus for the frontispiece. Jennifer Read,
Carleton University, assisted with all aspects of the art work, and
her assistance is gratefully acknowledged. All scanning electron
micrographs were taken from uncoated specimens by Lewis Ling, Carleton
University, whose efforts are greatly appreciated. Donald R.
Whitehead, Systematic Entomology Laboratory, Washington, read the
manuscript and provided many helpful comments.
I especially thank my husband, Henry F. Howden, for patiently
advising and discussing ideas and for assisting with the many more
tedious aspects of preparing the manuscript for publication.
LITERATURE CITED
Bates, H. W.
1910. The naturalist on the River Amazons. Popular Edition.
John Murray, London. 394 pp.
Blackwelder, R. E.
1957. Checklist of the Coleopterous insects of Mexico, Central
America, the West Indies, and South America. USNM. Bull.
185: 1-1492.
Blanchard, E.
1846, In Brullé, A., 1843, Insectes de 1'Amérique méridionale
recueillis par Alcide d'Orbigny, et decrits par Emile
Blanchard. Paris. pp. 105-222 (= 1846 Blackwelder
1957:968).
Howden: Hadromeropsis 129
Boheman, C. H.
1840. In Schoenherr, Genera et species curculionidum, cum
synonymia hujus familiae. Vol. 6, pt. 1. Roret, Paris.
1845. In Schoenherr, Genera et species curculionidum, cum
synonymia hujus familiae. Vol. 8, pt. 2. Roret, Paris.
504 pp.
Brown, F. M.
1941. A gazetteer of entomological stations in Ecuador. Ann.
Ent. Soc. Amer. 34: 809-851.
Champion, G. C.
1911. Otiorhynchinae alatae. In Biologia Centrali-Americana,
Coleoptera 4(3): 178-354.
Ciark. W. Be
1977. Male genitalia of some Curculionoidea (Coleoptera):
musculature and discussion of function. Coleopt. Bull.
31(2): 101-115.
Fassl, A. H.
| 1915. Tropische Reisen. V. Das obere Caucatal und die
Westcordillere. Ent. Rund. (1914) 31(10): 57-58,
Faust, J.
1892. Reise von E. Simon in Venezuela. Curculionidae. Stett.
Ent. Zeit. 53: 1-44,
Giibert,.£. E.
1952. The homologies of the male genitalia of Rhynchophora and
allied Coleoptera. Ann. Ent. Soc. Amer. 45(4): 633-637.
Gunther, L., and F. Zumpt.
1933. Curculionidae: Subfam. Tanymecinae. Coleopterum
catalogus. Pars 131. Junk, Berlin. 131 pp.
Hayward, K. J.
1960. Insectos Tucumanos Perjudiciales. Rev. Industrial y
Agricola de Tucuman 42: 144, 1958 (1960).
Heller, K. M.
921. Nuevos Curculionidos de 1a _ Argentina. BA. © SOC:
Cientifica Argentina 1921: 19-35.
Horn, G. H.
1876. In Leconte, John L., and George H. Horn, The Rhynchophora
of America North of Mexico. Proc. Amer. Phil. Soc. 15
(96): 455 pp.
Howden, A. T.-
1959. A revision of the species of Pandeleteius Schonherr and
Pandeleteinus Champion of America North of Mexico
(Coleoptera: Curculionidae). Proc. Calif. Acad. Sci. 29
(10): 361-421,
1966. Airosimus, a new genus of neotropical Tanymecini
(Coleoptera: Curculionidae). Trans. Amer. Ent. Soc. 92:
173-229. |
1969. The genus Pandeleteinus Champion with the description of
a new species from Mexico (Curculionidae, Tanymecini).
Coleopt. Bull. 23 (3): 76-83,
1976. Pandeleteius of Venezuela and Colombia (Curculionidae:
Brachyderinae: Tanymecini). Mem. Amer. Ent. Inst. No. 24.
310 pp.
130 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Howden, H. F., andJ. M. Campbell.
19 Observations on some Scarabaeoidea in the Colombian
Sierra Nevada de Santa Marta. Coleopt. Bull. 28 (3):
109-114.
Hustache, A.
1928 (1926). Curculionides de 1a République Argentine
(Premi@re note). Anales del Museo Nacional de Historia
Natural "Bernardino Rivadavia’ 34: 155-261.
1938. Curculionides de 1‘Argentine et des regions limitrophes.
Rev. Soc. Ent. Argentina 10 (1): 3-17.
International Commission on Zoological Nomenclature.
1964. International code of zoological nomenclature adopted by
the 16th International Congress of Zoology. International
Trust for Zoological Nomenclature, London: 176 pp.
Kirsch, T.
1867. Beitrage zur Kaferfauna von Bogota. (Drittes Stuck:
Brenthiden und adelognathe Curculionen.). Berl. Ent.
Zeitschr. 11: 216-243.
1873. Beitrage zur Kenntniss der Peruanischen Kaferfauna auf
Dr. Abendroth's Sammlungen basirt. Berl. Ent. Zeitschr. 17
(1): (121-152.
Kuschel, G.
1955. Nuevas sinonimias y anotaciones sobre Curculionoidea.
Rev. Chilena Ent. 1955 (4): 261-312.
kucas, Pen. :
1857. (=1859?). Entomologie. In Animaux nouveaux ou rares
recueillis pendant 1'expédition dans les parties centrales
de 1'Amérique du Sud, de Rio de Janeiro a Lima, et de Lima
au Para; exécutée par ordre du gouvernement Francais
pendant les années 1843 a 1847, sous la direction du Comte
Francis de Castelnau. Paris. 204 pp.
Marshall, G. A. K.
1952. Taxonomic notes on Curculionidae (Col.). Ann Mag. Nat.
Hist. (12)°5: 261-270.
Ohaus, F.
1908. Die Ruteliden meiner Sammelreisen in Sudamerika (Col.).
Deutsch. Ent. Zeitschr. 1908: 239-262, 383-408.
Olivier, A. G.
1807. Entomologia, ou histoire naturelle des insectes, avec
leurs caractéres génériques et spécifiques, leur
description, leur synonymie, et leur figure enluminée.
Coléoptéres. Vol. 5. Desray, Paris. 612 pp.
Papavero, N.
1971. Essays on the history of Neotropical Dipterology. Vol.
1. Museu de Zoologia, Universidade de Sao Paulo, Sao
Paulo, 216 pp.
Pascoe, F. P.
1881. New Neotropical Curculionidae.-Part IV. Ann. Mag. Nat.
Hist. (5) 7: 38-45.
Pierce, W. D.
1913. Miscellaneous contributions to the knowledge of the
weevils of the families Attelabidae and Brachyrhinidae.
Proc. U.S.N.M. 45 (1988): 365-426.
Howden: Hadromeropsis 131
Schoenherr, C. J.
1823. Curculionides. Tabula synoptica familiae curculionidum.
Isis Oken, 1823, col.: 1133-1146.
1826. Curculionidum dispositio methodica cum generum
characteribus, descriptionibus atque observationibus
variis, seu prodromus ad synonymiae insectorum. Partem 4.
Lipsiae. 338 pp.
1833. Synonymia insectorum, oder Versuch einer Synonymie aller
von mir bisher bekannten Insecten. Mit Berichtigungen und
Anmerkungen, wie auch mit Beschreibungen neuer Arten. Band
1, Teil 4. Roret, Paris. 381 pp.
1834. Genera et species curculionidum, cum synonymia hujus
familiae. V¥oty 2, pt. 3. Roret, Paris. 326 pp.
Selander, R. B., and P. Vaurie.
1962. A gazetteer to accompany the "Insecta" volumes of the
"Biologia Centrali-Americana." Amer. Mus. Nov., No. 2099,
70 pp.
— Snarp, De-E.
1918. Studies in Rhynchophora. A preliminary note on the male
genitalia. Trans. Entomol. Soc. London. 66:209-222.
1920. Studies in Rhynchophora. IX. The sexes of Bog ga
brevisetis Champ. J.N.Y. Entomol. Soc. 28(1):
Simon, E.
1889. Voyage de M. E. Simon au Venezuela (Decembre 1887 - Avril
1888) 4e Memoire, Arachnides. Ann. Soc. ent. Fr., Aout
1889: 169-220.
Spteth, Hv-d«
1950. The David Rockefeller Mexican expedition of the American
Museum of Natural History. Introductory Account. Amer.
Mus. Nov. No. 1454: 1-67,
Thompson, R. T. |
1977. A revision of the New Guinea weevil genus Apirocalus
Pascoe (Coleoptera: Curculionidae). Bull. Brit. Mus. (Nat
Hist.) Ent. ser. 36(5): 193-280.
Van Dyke, E. C.
1943. Additional new species of west American Coleoptera.
Pan-Pacific Ent. 19 (13): 101-108.
Van Emden, F. I.
1944. <A key to the genera of Brachyderinae of the world. Ann.
Mag. Nat. Hist. (11) 11: 503-532, 559-586,
¥oss, E.
1953. Neue und bemerkenswerte Curculioniden aus Columbien und
Bolivien. (118. Beitrag zur Kenntnis der Curculioniden).
Entomologische Mitteilungen 1953 (2): 55-84),
1954. Curculionidae (Col.). In Beitrage zur Fauna Perus. Bd.
IV: 193-376.
132 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 2-12. H. (Hadromeropsis) spp. habitus. 2-3, superbus,
female: 2, dorsal; 3, lateral. 4-5, meridianus, male: 4, dorsal; 5,
lateral. 6, gemmifer, male, dorsal. 7-10, argentinensis: 7, female,
dorsal; 8, male, dorsal; 9, male, lateral; 10, female, lateral. 11,
speculifer, female, dorsal. 12, pulverulentus, female, dorsal.
Howden: Hadromeropsis 133
Figs. 13-21. H. (Hadromeropsis) spp. habitus. 13, togatus,
female, dorsal. 14, nobilitatus, female, lateral. 15-17, ieeane:
15, male, dorsal; 16, female, dorsal; 1/7, female, lateral.
atomarius, female: 18, dorsal; 19, lateral. 20-21, pallidus, female:
20, dorsal; 21, lateral.
134 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 22-25, 27. H. (Hadromeropsis) spp. habitus. 22-25,
beverlyae: 22, male, dorsal; 23, male, Tateral; 24, female, dorsal;
25, female, lateral. 2/, fasciatus, female, dorsal.
Figs. 26, 28. H. (Hadrorestes) spp. habitus. 26, alacer, female,
dorsal. 28, dialeucus, female, dorsal.
Howden: Hadromeropsis ISD
Figs. 29-38. H. (Hadrorestes) spp. habitus. 29, institulus,
female. 30, apicalis, female. 31, picchuensis, female. 32, scambus,
female. 33, transandinus, male. 34, conquisitus, female. 30,
pectinatus, male. 36, magicus, male. 37, contractus, female. 38,
spiculatus, male.
136 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 39-46, H. (Hadromeropsis) spp. 39, opalinus, female, head,
lateral view. 40, crinitus, male, head, lateral view. 41, fulgens,
male, head, anterior view. 42, crinitus, male, head, anterior View.
43, crinitus, male, epistoma. 44, dejeanii, male, head, anterior
view. 45, flagellatus, male, head, anterior view. 46, fulgens, male,
epistoma.
Howden: Hadromeropsis 137
Figs. 47-52. H. (Hadromeropsis) spp. 47, crinitus, male, apex of
elytra. 48, flagellatus, male, femoral flange. 49, aureus, male,
prothorax, dorsal view. 50, cretatus, male, head and prothorax,
lateral view. 51, aureus, male, apex of elytra, lateral view. 52,
cretatus, male, apex of elytra, lateral view.
138 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 53-58. H. (Hadromeropsis) spp. 53, aureus, male, apex of
elytra, lateral view. , cretatus, female, apex of elytra, lateral
view. 55-58, gemmifer: 55, male, head, anterior view; 56, female,
head, anterior view; 5/7, male, coxal tubercle; 58, female, coxal
tubercle. |
Howden: Hadromeropsis 139
ane
abdomen; 60, meridianus, female, abdomen. 61, gemmifer, male, fore
leg, ventral view. 62, rufipes, female, apex of elytra, lateral view.
63-65, batesi, male: 63, head, anterior view: 64, apex of rostrum; 65,
distal end fore femur.
Figs. 59-65. H. (Hadromeropsis) spp. 59, gemmifer, female,
140 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
67
Figs. 66-72. H. (Hadromeropsis) spp. fore tibia. 66, fulgens,
male, Cuernavaca. 67, Opalinus, male, Durango. 68, flagelTatus,
male, Apizaco. 69, scintillans, male, lectotype, Quiche Mts. /0,
micans, female, lectotype. /1, dejeanii, male, Playa Vicente. /72,
rufipes, female, type.
Howden: Hadromeropsis 141
Figs. 73-83. H. (Hadromeropsis) spp. male genitalia. 73,
fulgens, aedeagus with flagellum atypical paralectotype from Amula.
74-76, Opalinus: /4**, proximal end of flagellum, lateral view; 75,
aedeagus with flagellum; /76**, proximal end of flagellum, ventral
view. //, crinitus, aedeagus. /8-81, flagellatus: 78, aedeagus with
flagellum; 79**, proximal end of flagellum, ventral view; 80,
genitalia in normal position in abdomen, thorax removed; 81**,
proximal end of flagellum, lateral view. 82-83, dejeanii: 82,
aedeagus with flagellum; 83**, proximal end of flagellum, Tateral
view.
**shown 6x larger than unmarked figures
142 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 84-100. H. (Hadromeropsis) spp. male genitalia. 84-86,
amoenus: 84, aedeagus with flagellum; 85**, proximal end of flagellum,
ventral view; 86**, as 85, lateral view. 8/-89, scintillans: 87,
aedeagus with flagellum; 88**, proximal end of flagellum, ventral
view; 89**, as 88, lateral view. 90-91, brevicomus: 90, aedeagus
with internal sac extruded; 91**, flagellum. 92-94, aureus: 92,
aedeagus; 93*, flagellum; 94**, proximal end of flagellum ventral
view. 95-97, cretatus: 95, aedeagus with flagellum; 96**, proximal
end of flagellum, lateral view; 9/7**, as 96, ventral view. 98-100,
superbus: 98, aedeagus; 99, flagellum; 100**, proximal end of
flagellum, lateral view.
*shown 3x longer than unmarked figures
**shown 6x larger than unmarked figures
Howden: Hadromeropsis 143
101
Figs. 101-111. H. (Hadromeropsis) spp. male genitalia.
gemmifer: 101, aedeagus; 102**, internal sac; 103**, "flagellum",
ventral view. 104-107, meridianus: 104, aedeagus; 105*, flagellum;
106**, proximal end of flagellum, ventral view; 107**, proximal end of
flagellum, lateral view. 108-111, batesi: 108, aedeagus and dorsal
view of apex; 109*, sternite 8, ventral view; 110**, proximal end of
flagellum, ventral view; 111, spiculum gastrale.
*shown 3x larger than unmarked figures.
**shown 6x larger than unmarked figures.
101-103,
144 Contrib, Amer... tnty netig voro los no. 6, 1982
112 113
%
116 17 118 119
120 121 122 123
124 125 127
P ae Yulus
= cornu
ramus
128 130
Figs. 112-130. 6H. (Hadromeropsis) spp. spermatheca. 1123
opalinus, 113-115, flagellatus. 116, fulgens. 117, crinitus. 118,
dejeanii. 119, micans. 120, scintillans. 121, amoenus. 122-123,
brevicomus. 124, aur aureus. 125, cretatus. 126, superbus. id,
gemmi fer. 128- 129, meridianus. 130, batesi.
Howden: Hadromeropsis 145
te Vos
ee
138 139
140
141
142
143
144 145
146
Figs. 131-146. H. (Hadromeropsis) spp. 131-139, ventrite 5: 131,
crinitus, male; 132-133, flagellatus: 132, male; 133, female; 134,
amoenus, male; 135, amoenus, female; 136, scintillans, male; 137,
scintillans, female; 138, rufipes, female; 139, micans, female. 140,
Speculifer, male, fore tibia. 141-142, excubitor, apex fore tibia:
rT. male; 142, female. 143, speculifer, female, abdomen. 144-145,
atomarius, fore tibia: 144, male; 145, apex, female. 146, fasciatus,
male, fore tibia.
146 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 147-152. H. (Hadromeropsis) spp. 147, plebeius, female,
apex of elytra, lateral view. 0, pulverulentus, female: 148,
apex of elytra, lateral view; 149, head, anterior view; 150, base of
elytra, dorsal view. 151, pallidus, male, rostrum, oblique view.
152, beverlyae, male, fore leg, posterior view.
Howden: Hadromeropsis 147
Figs. 153-158. H. (Hadromeropsis) spp. 153, opalinus, male, apex
fore tibia. 154, beverlyae, male, apex fore tibia. , atomarius,
female, abdomen. , Deverlyae, male, rostrum. 157-158, fasciatus,
female: 15/7, apex of elytra, lateral view; 158, apex of rostrum,
dorsal view.
148 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
male genitalia. 159-160,
161-162, argentinensis:
Figs. 159-167. H. (Hadromeropsis) spp.
togatus: 159**, internal sac; 160, aedeagus.
I61**, internal sac; 162, aedeagus. 163, pulverulentus, aedeagus.
sac; 165, aedeagus. 166-167,
164-165, plebeius: 164**, internal
166, aedeagus; 16/**, internal sac.
pallidus:
shown 6x larger than unmarked figures
Howden: Hadromeropsis 149
4
>
eo eres oD
175
Figs. 168-176. H. (Hadromeropsis) spp. male genitalia and rectal
169, aedeagus.
ring. 168-169, speculifer: » internal sac;
170-171, beverlyae: , internal sac; 1/1, aedeagus in lateral view
and apex in dorsal view. 1/72*, flagellatus, rectal ring. 173-174,
nobilitatus: 173, aedeagus; 174**, internal sac. 175-176, atomarius:
175, aedeagus; 176**, internal sac.
*shown 3x larger than unmarked figures
**shown 6x larger than unmarked figures
150 Contrib.) Amer. °Entscinstsy'vo lhe 19;.no.:6, 1982
Figs. 177-180. H. (Hadromeropsis) spp. male genitalia. 1//-178,
excubitor: 177, aedeagus; , internal sac. 179-180, fasciatus:
1/9, aedeagus; 180**, internal sac.
**kshown 6x larger than unmarked figures
Howden: Hadromeropsis Loy
193 194 195
191 192 :
\ L 197 198
Figs. 181-200. H. (Hadromeropsis) spp. female genitalia.
181-182, argentinensis: 181*, bursal sclerite, ventral view; 182,
genitalia, setae omitted. 183, ulverulentus, genitalia, setae
omitted, including ventral view of bursal sclerite. 184, pee
spermatheca. 185, speculifer, spermatheca. 186, plebeius,
Spermatheca. 18/7, pallidus, spermatheca. 188-190, beverlyae: 188,
genitalia; 189*, bursal sclerite, oblique view; 190*, bursal sclerite,
dorsal view. 191, nobilitatus, spermatheca. 192-194, "smooth"
nobilitatus, spermatheca, three examples of variation. 195,
atomarius, spermatheca. 196-198, excubitor, spermatheca, three
examples of variation. 199-200, fasciatus, spermatheca, lateral and
edge views.
*shown 3x larger than unmarked figures
199 200
152 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 201-206. H. (Hadrorestes) spp. 201-203, alacer, male: 201,
dorsal habitus, paratype from Baeza; 202, apex of elytra, type, dorsal
view; 203, elytral sculpture at suture medially, paratype from Baeza.
204, inconscriptus, female, elytral sculpture at suture medially.
205, nebulicolus, female, elytral sculpture at suture medially. 206,
silaceus, male, elytral sculpture at suture medially.
Howden: Hadromeropsis 153
Figs. 207-213. H. (Hadrorestes) spp. 207-209, alacer: 207,
prothorax, dorsal view, type; 208, prothorax, dorsal view, male from
Baeza; 209, fore femur, outer edge, male from Baeza. 210-213,
impressicollis: 210, female, head, antero-lateral view; 211, ventrite
9, female; 212, prothorax, dorsal view, male; 213, prothorax, dorsal
view, female.
154
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 214-219. H. (Hadrorestes) spp. 214, impressicollis,
female, apex of elytron, dorsal view. 215-218, institulus, female:
215, apex of elytron, dorsal view; 216, head, antero-Tateral view;
217, prothorax, dorsal view; 218, abdomen and edge of elytra. 219,
bombycinus, prothorax, female, lateral view.
155
is
Hadromerops
Howden
a Y na an A
AISM Vn] WV
SO OQh.Siez
cCyew &]/ 3s
Tell (ad Tall
OlQ «>» OW
(oem) "Goen
Q = &
El CE
rege
eT
QJ op)
os © ska =
See
1 Ge =
o °7f. a
WI =z
Nx So &
wo ofc 2
2. o|>
oY Si
aS An
= Sere
" r
T,) ak AI
a
Nq wv
Nat
7) 1 =
wiencr © e
Ppl e7Tn =
nl on a Vv
rab ies DD) o-=
Ce aed
l=
ol, YVo—
oi/C TS wo
- >o
Cig See
Ps Pa)
coo a & ®
=< Eat = &
= = ON —
ae >
i A
Sou Ee
or = 30
wit aYVOor
NS o> = @
N Sor VE
iq +o
© xt} Ye
qn Oo ©
No oe: e
N =
NNYES
e QI (az
” = $.
TH oc on TO a Y&
‘= Orc Vo
tiem TSC arm N
CNT 8B
ee So
vodoevdws
ee OH E
156 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 227-232. H. (Hadrorestes) spp. 227-230, brachypterus,
female: 227, prothorax, dorsal view; 228, apex of elytra, oblique
dorsal; 229, dorsal habitus; 230, ventrites 3, 4, and 5. 231-232,
transandinus, female: 231, habitus, lateral view; 232, apex of elytra,
lateral view:
Howden: Hadromeropsis 157
Figs. 233-238. H. (Hadrorestes) spp. 233-234, transandinus: 233,
head, female, anterior view; 234, prothorax, male, dorsal view.
235-237, apicalis, female: 235, head, anterior view; 236, prothorax
and base of elytra, dorsal view; 237, apex of abdomen and elytra,
ventral view. 238, nanus, male, head and prothorax, dorsal view.
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 239-244. H. (Hadrorestes) spp. 239-242, nitidus, male;
239, prothorax, dorsal view; 240, metasternum, base of elytra, lateral
view; 241, apical portion of elytra, dorsal view; 242, apex of
rostrum, dorsal view. 243-244, mandibularis, female: 243, head,
anterior view; 244, apex of rostrum.
Howden: Hadromeropsis 159
Figs. 245-250. H. (Hadrorestes)
245, prothorax, female, dorsal view; 246, fore femur, male, anterior
spp. 245-248, mandibularis:
view; 247, apex of elytra, male, dorsal view; 248,
female, dorsal view.
view; 250, abdomen.
apex of elytra,
249-250, magicus, female: 249, prothorax, dorsal
160 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 251-256. H. (Hadrorestes) spp. 251-253, magicus: 251, base
of elytra, male, lateral view; 252, base of elytra, female, lateral
view; 253, apex of elytra, female, Jateral view. 254-256,
conquisitus: 254, apical portion of elytra, female, dorsal view; 255,
prothorax, holotype, male, glabrous, dorsal view; 256, prothorax,
male, squamose specimen, dorsal view.
Howden: Hadromeropsis 161
:
"
_ .
Figs. 257-262. H. (Hadrorestes) spp.
257, fore femur, posterior view; 258, fore leg, anterior view; 259,
apex of elytron, dorsal view. 260-262, scambus: 260, apex of elytron,
female, dorsal view; 261, apex of elytron, male, dorsal view; 262,
fore leg, female.
257-259, conquisitus, male:
Contrib. Amer. Ent.
Figs. 263-268. H. (Hadrorestes) spp. 263-264, scambus, female:
263, head, anterior view; 204, head and prothorax, Tateral view.
265-268, pectinatus: 265, head, type, male, anterior view; 266,
prothorax, type, male, dorsal view; 267, fore leg, male from Colombia,
anterior view; 268, apex of elytra, female, dorsal view.
Howden: Hadromeropsis 163
Figs. 269-274. H. (Hadrorestes) spp. 269-270, pectinatus,
allotype: 269, abdomen; 2/70, detail of caudal surface ventrites 2, 3,
and 4, 2/1-2/73, picchuensis, female: 2/1, head and prothorax, dorsal
view; 2/2, apex of elytra, dorsal view; 2/3, elytra, caudal view.
2/4, contractus, head, female, anterior view.
Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
164
Aen HK
“nIzn
3/0 3
Him O
Ol> 3
im <5)
pis
P|5 «6
S1— =
Ol, UO
Vly
H a
a =
fc AN
A
aos
LC Oe
~~ ee
at:
7 3
oU
“gy.
Q. 0]
(ax
Yn aA
LO -*
ae
Ql
“nl ™
Wien
1S ea
Yio =
Orr w
S| > oe
‘o) >
o
31S
ss
ad
Og
Go
Z oO
Nn
a :
© 6
Oo =}
eer
Oy ry
Co
ae
lp
~ ew
Oo ©
Ke)
MM
oS
n 2.
Neer
= Wd
ETSY
Gia
om~m
Yr
Gee J
apex of
9
Vv
=
oS
&
<8)
qe
v)
Ss
ras)
is]
=
O
=
—”
©
o@)
N
=
cob)
cre
>
pa
GS
e)
ae
(e)
sw)
ive]
Ss
‘<a
=
— o
Vr
>
rT
ox
iso]
<x nN
yD
a. Oo
cw
3
3
female
elytra
-Howden: Hadromeropsis 165
Figs. 281-287. H. (Hadrorestes) spp. 281, dialeucus, female,
prothorax, dorsal view. 282-285, cavifrons, female: 282, head,
oblique lateral view; 283, prothorax and head, dorsal view; 284, hind
tibia, outer view; 285, apex of elytron, dorsal view. 286-287,
spiculatus, male, fore leg: 286, anterior view; 287, posterior view.
166 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
yyy
_
Fig. 288. H. (Hadrorestes) spiculatus, male, head and prothorax,
dorsal view.
Figs. 289-293. Hadromeropsis earinus, female: 289, head, dorsal
view; 290, prothorax, dorsal view; 291, apex of elytra, lateral view;
292, abdomen; 293, detail of caudal edge of ventrites 2, 3, and 4.
Howden: Hadromeropsis 167
eid
ZL Ween.
303
304
305
307
S, 308 309
Figs. 294-309. H. (Hadrorestes) spp. 294-301, ventrite 5: 294,
alacer, male; 295, ~ alacer, female; 296, nebulicolus, male; 297,
silaceus, male; 298, inconscriptus, male; 299, inconscri inconscriptus, female;
300, nitidus, male; 301, magicus, male. 302- 3 fore tarsus: 302,
alacer, male; 303, impressicollis, male; 304, inconscriptus, male;
305, transandinus, female; 306, nebulicolus, male; SUF dialeucus,
male; 308, pectinatus, male; 309, silaceus, male.
168 Contrib. Amer« EnOiinsts,: vorpulg, no. 6, 1982
Figs. 310-319. H. (Hadrorestes) spp. male genitalia. 310-311,
alacer: 310**, apex of internal sac; 311, aedeagus. ple".
inconscriptus, apex of internal sac. 313-314, nebulicolus: 313%**,
apex of internal sac; 314, aedeagus. 315-316, silaceus: 315, aedeagus
and apex of aedeagus in dorsal view; 316**, apex of internal sac.
317-319, impressicollis: 317**, apex of internal sac; 318, tegmen;
319, aedeagus.
**shown 6x larger than unmarked figures
Howden: Hadromeropsis 169
Figs. 320-328. H. (Hadrorestes) spp. male genitalia. 320-321,
nanus: 320, aedeagus (sac not completely extruded); 321**, apex of
internal sac. 322-323, transandinus: 322, aedeagus; 323**, apex of
internal sac. 324-325, dialeucus: 324, aedeagus; 325**, apex of
internal sac. 326, scambus, aedeagus. 327, spiculatus, aedeagus.
328**, pectinatus, apex of internal sac.
*kshown 6x larger than unmarked figures
170 Contrib. Amer, Ent. Inst., vol. 19, no. 6, 1982
333
GEG 334 335
Figs. 329-334. H. (Hadrorestes) spp. male genitalia. 329-330,
conquisitus: 329, aedeagus; 330**, apex of internal sac. 331-332,
magicus: 331, aedeagus; 332**, apex of internal sac. 333-334,
nitidus: 333**, apex of internal sac; 334, aedeagus.
Fig. 335*. Hadromeropsis earinus, spermatheca.
*shown 3x larger than unmarked figures
**shown 6x larger than unmarked figures
Howden: Hadromeropsis 171
Figs. 336-340. H. (Hadrorestes) spp. female genitalia. 336,
alacer. 337, silaceus. 338, nebulicolus. 339, inconscriptus,
Spermatheca in lateral and edge view. 340, institulus, plus ventral
view of bursal sclerite. 341, bombycinus. 342, bombycinus, ventral
view of bursa copulatrix with common oviduct pulled aside.
172 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
Figs. 343-348. H. (Hadrorestes) spp. female genitalia. 343,
transandinus, including edge view of spermatheca. 344, brachypterus,
including edge view of spermatheca. 345, apicalis, including edge
view Of spermatheca. 346, mandibularis, including edge view of
Spermatheca. 34/7, magicus. 348, nitidus, including edge view of
Spermatheca.
Fig. 349. H. (Hadromeropsis) argentinensis, spiculum ventrale.
Howden: Hadromeropsis 173
-
t
t
1
{
{
\
\
\
\
Figs. 350-357. H. (Hadrorestes) spp. female genitalia. 350,
conquisitus. 351, scambus, including edge view of spermatheca. 352,
ectinatus. 353, picchuensis, up ventral view of bursa copulatrix
with common oviduc pu aside. 354, contractus, plus second
example of lateral he ike TOD dialeucus. 356, cavifrons,
including edge view of spermatheca. 357, spiculatus.
Contrib. Amer. Ent.-Inst., vol. 19, no. 6, 1982
174
fore
0c.
head, anterior
apex of elytra,
iew
360
dorsal v
3
358
3
V1ew
3
triatus male.
latera
ight elytron
ew.
is s
“gh
Hadromerops
prothorax
center of r
ior v
anter
b
e
3
-362
head an
361
tal half
358
3
View
d
is
igs.
igs.
359
F
Ta
e
view
j
dorsal
t
363, head,
male.
view.
1S
1
]
) exi
latera
3
(Hadrorestes
head and prothorax
H
, 364,
, 2648
363
jew
1or Vv
F
anter
Howden: Hadromeropsis 175
365
368
&
a 1% As
© Rake : A D>.
SS} ae SS ¥
= >»
Ee. SEES
Rs VER
Gr. + NOE EIEA
bene
S 2
369 “© 370
Figs. 365, 366. H. (Hadrorestes) exilis male a haialta 365,
aedeagus; 366*, internal sac.
Figs. 367%, H. (Hadromeropsis) rufipes spermatheca.
Figs. 368-370. Hadromeropsis striatus male. 368, aedeagus;
3697*. internal: ¢a¢;.370, Ventrite D.
*shown 3x larger than unmarked figures
**shown 6x larger than unmarked figures
1/6 Contrib. Amer. Ent. Inst., vol.
£9. sno. 6, 1962
' —- aA
Map l
ep er initus A. sp.
@ dejeanii (Boheman)
@ fulgens (Champion)
A Opalinus (Horn)
Map 2
@ brevicomus n. sp.
M fiagellatus n. sp.
* rufipes (Champion)
Howden: Hadromeropsis 177
: ‘ ih Led
“ Pleas Oe cee
} : ees 5
. pee Rie ’
om C 2: 4 /
gn 0
‘ : ?
Be NT Se eae at ee te ere eee
i Sa
w
a4 >. =
iv ae 4 =
~ ? va 79 wa
Cro ry c
At Th >:
een Bh t
nes :
ae
\-
@ amoenus n. sp.
* cretatus (Champion)
% micans (Champion) '
@ scintillans (Champion) ; e
ws ewe
Map 4
aureus (Blanchard)
Datesi n. sp.
gemmifer (Boheman)
meridianus n. sp.
Superbus (Heller)
KPO <
178 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
8 Map 6
Lila @ beverlyae n. sp.
® epee nels 1s (Hustache) @ fasciatus (Lucas)
* plebeius n. sp. Dallit
* pallidus n. sp.
@ togatus (Boheman) wk pulverulentus n. sp.
Map / Map 8
@ excubitor n. sp. *% atomarius (Boheman)
@ speculifer n. sp. @ nobilitatus (Gyll.)
Howden: Hadromeropsis 179
Map 9 Map 10 .
@ alacer n. Sp. @ apicalis n. sp.
% inconscriptus n. sp. ae Warns oN. SP.
% nebulicolus n. sp. *% transandinus n. sp.
M silaceus n. sp.
SFA ow.
Map 12
3 conquisitus n. sp.
G6 contractus n. sp.
1 magicus (Pascoe)
1 ' 2 nitidus n. sp.
m impressicollis (Kirsch) 5 picchuensis n. sp.
* institulus n. sp. Sa
4 spiculatus n. sp.
Map 11
@ bombycinus n. sp.
ee a rca me a
180 Contrib. Amer. Ent. Inst., vol. 19, no. 6, 1982
is
*
RQ
.
f)
°
$e
f sD
u [J
3f
wee
Ws, «
s ff
: ;
e \ '
ig Lee * Hq 4
‘ . ' i
. ai) ” i (Ee
& ie te
i N
f .. mn
aa
o hy
Ps ‘ a
f saat
ys
‘ ie
A,
( ees
4 f x ,
1 t .
é
X
t
j
4
;
Ly
)
hs
5 4
ve fk
{by
a)
a
re
si
% 7b
bh
xi ad
A
w
Map 13
3 cavifrons n. sp.
1 mandibularis n. sp.
4 pectinatus n. sp.
2 scambus n. sp.
THE ICHNEUMONID PARASITES ASSOCIATED WITH THE
GYPSY MOTH (LYMANTRIA DISPAR)
By
VIRENDRA GUPTA
Center for Parasitic Hymenoptera
Institute of Food and Agricultural Sciences
University of Florida, Gainesville, Florida 326ll
This research was financed by the U. S. Department of Agriculture,
Systematic Entomology Laboratory, Washington. It was started at the
American Entomological Institute, Ann Arbor, and completed at the
Center for Parasitic Hymenoptera, Gainesville.
CONTENTS
ee rtion,. oo ee a ee ee eee
Ba otenial and Methods 5 nes es ok ee a ee
PCKNOWLECASIIONIS . «6 oii ee er gar aa wpe Ow) WO i Re Se We 8 ew 8
List I. Ichneumonidae that are parasitic upon the gypsy moth. .....
List II. Ichneumonidae that are doubtful or occasional parasites of the
PYNSY MOU Fo. . e e e ee e
List III. Ichneumonidae that are excluded as gypsy moth parasites... .
List IV. Ichneumonid parasites associated with Lymantria obfuscata
Key to the subfamilies of Ichneumonidae associated with the gypsy moth
1, Subfamily PIM PLINAE (Bpnialtinae) 6 2s ee ee
EYUOG TOOWiGIINae ee ces ok se pee ee ee ee
1, GONUs COCO CONUS. ..5.. ~, enn a ee
Ass GODS 11091 COIS a a a a a a
3. GODS POhigies:. ot le a oe a
Tipe TAOTOUli 0 oe ee ee ee
a. Gens Thevona 2... ke eee ee ae a ee
Tipe Pimpin. 4266 bee os ea ae
5, (/GOWUS ACrORUDIa 3) 65. ON ee es
O. Gennes iseyopus ee ee ee ee ys
Bee mesa ily POT ON LINE ica actiainral ve See as Gn eae ia. aa
Genus O1NOPLOTUS 6. 6 ORI OO Pee eh gg
OTUS COUPON Oe. ee Oa ee PO Br Sn,
Genus Costar oo ee eee re es
CONN COV Ol Se hace a 5 ow ke ek le a ee
CONUS POD OCO IDE «a de os J kk a ee a
Crome MVPOS OIE 16 Slee ae Tek. RK Ow
Oor WH =
i, Subtamily ICH NEEM ONIN ee es ee woe
Tribe Ichneumonini (=Protichneumonini)..............
hs, ABONGS, LVIBOMIPICHHOCUNION. oa ecncw ces bc kow a me hkl 4
2 > (ZONES PAV COGLLCHNOCUNION: cc. be os clk Ghee ay eo
oi Gene Celene: ao: eae el beer
4. “Goma Jokneunian oie oo PRO as, eno tae ae
TEV Nae ea ke aes ik ee a ea eae
DME Vy Se MRC cea oT) ame mae DOR aE Se eesti me sy tt GEE ra ely Nene Gor nitee
6. 7, QO MCIGniCRNCUNION 6 Bi BOR ERE RE
1. Gene Crooner Or PO ee OR.
Bi OT Ce ee ee ee es ie Aa eae is
LO, Gomme: Pep roeya ae nk ek a ee lea) ake wre a en
A RO tie id ah i ie ey a ree
Res IOUT i ORCI O Se SO a Mi ak ae Ok ews
li
iil
TYING PRISTICEVOUIE A eo ek hk hs Ba ks i eheniess, Pate Laie 103
toy SGOIIS COPE eS Iay CIES... vibes ce. beck ee RoR ees 103
TV. UDEQUIELY tr ET ee ee ek eck ew ke ee 104
te ene re a ee eS we ae 106
et ee es ele a ae ie ek Pe 107
Oe TCR TS GAAS TELCO IU NLR CIR Pee iane . e hy 108
Vie OU ee 6 gh a eae we A ne ee ea a a 110
Bs ERS d tee a ok eR oe dan ac 110
Mie NG Cet a sho kk ra ae ts oe Ce pla Ge be GS 112
Ee PU Pee coy OR RO V0 Ue ee Ne SG 112
Vids -Subiamily CREM AGT INAE syccss go k VeSTSIA a BIO, A ae 115
Dee 6s ee ee aa we ES See 115
W til. ty NOTA LIAR, os ica sci os SOURS ENO. UP oe a 117
ac Gere 7 PICHON A 1 Chonmela). 6a ok rk ee 118
Pe a ee ass es Fa MS, OGRA 119
i RS a ek oa, RR BR, a, 120
Pr ey OP Re I a ek Se oleh oa ely wk a ak ees 121
Dis RE. DOIN. enki saves a eT ees “TARR Es 121
Oe CIES BPI COSD TAS. ee OIG BGR al a, 122
Pe Se PDEA ey ek ce yee ts cate ee SER GG 124
A. Seay PCOLORA TINA sci isi ce WER BG a ees ao, 124
Ee Oe Se a eg ies ae A RE AE wn Loe Se ae
Pe ee i ae ee ks Lace ep EE UI BEE
THE ICHNEUMONID PARASITES ASSOCIATED WITH
THE GYPSY MOTH (LYMANTRIA DISPAR)
INTRODUCTION
The gypsy moth, Lymantria dispar, is an important defoliator of hardwood
trees, especially oaks, over much of Eurasia and Eastern North America.
Although the moth caterpillars prefer the oaks, they feed on the leaves of over
500 plant species (Forbush and Fernald, 1896, Mosher, 1915). Their enor-
mous feeding activity in seasons of outbreaks defoliate many important orna-
mental trees of great aesthetic value, such as the oaks, birch, poplars,
willows, maple, elms, etc. Repeated defoliations reduce the vigor of the trees
and secondary infestations by insects and diseases often kill the trees. The
conifers, which are also attacked, are more susceptible to defoliation, and one
complete defoliation by the gypsy moth may be fatal to the trees.
Ever since the escape of the gypsy moth into the forests of the New England
states before the turn of the century, intensive and extensive work has been
done in the United States to contain the pest and eradicate it. However, the
efforts have not been successful and the pest has continued to spread. During
the past eighty years or so, the pest has spread to most of the northeastern
states, extending westwards to Pennsylvania and southwards to Maryland. The
pest has also spread to certain pockets in Ohio, North and South Carolina,
Virginia, West Virginia, Michigan, Wisconsin, Washington and Oregon.
Since 1905, millions of parasites of various species have been imported
into the United States from Europe and Japan to control the gypsy moth. Only
ten of them got established, including only one ichneumonid, Phobocampe unti-
cincta. They have apparently not been very effective in checking the spread of
the moth. Two of them, Anastatus disparis and Ooencyrtus kuvande are egg
parasites; two, Apanteles melanoscelus and Phobocampe unicincta (= disparis),
parasitize smaller larvae (first to third instars); four, Blepharipa pratensis,
Compsilura concinnata, Exorista larvarum, and Parasetigena silvestris attack
mature larvae; and two, Monodontomerus aereus and Brachymeria intermedia
are pupal parasites. Hoy (1976) has given a list of all the species imported by
then and possible reasons for their non-establishment.
In Eurasia, the original home of the gypsy moth, there appears to be some
sort of a natural balance between the moth and its parasites. Yet periodical
outbreaks do occur in limited areas. It appears that the aggregate effect of
the introduced natural enemies and the indigenous parasites of the gypsy moth
in North America is approaching that which exists in Central Europe. In many
New England localities infested with the gypsy moth, the natural enemies have
been important factors in preventing outbreaks, or at least responsible for pro-
longing the intervals between the outbreaks.
The importance of the native ichneumonid parasites has also been under-
estimated. The success of a parasite has often been measured in terms of the
2 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
number of offspring a parasite is able to produce on the gypsy moth larvae or
pupae, rather than upon the damage and "killings" a parasite accomplishes
during the process of oviposition. A case in point is the work of Campbell
(1963), on the four native ichneumonid parasites of the gypsy moth: Itoplectis
conquisitor, Coccygomimus pedalis, Theronia atalantae fulvescens and T.
hilavis in Glenville, New York State. They attack the gypsy moth pupae.
They stung as many as 250 host pupae for each pupa that was parasitized
successfully (leading to the development of an ichneumonid offspring). He
further showed that the puncture wounds made by the ichneumonids while
stinging the moth pupae, permitted the entrance of the larvae of the Sarcopha-
gidae (which could enter the host pupae only when the integument was broken),
eventually killing the host pupa. About half of the stung pupae contained the
sarcophagid maggots.
By such an ichneumonid-sarcophagid relationship, and also by the mechani-
cal injury caused to the gypsy moth pupae by stinging, many of them fail to
produce adult moths. The ichneumonids, therefore, play a greater role in
controlling the gypsy moth than that is generally assigned to them.
In recent years there has been a renewed activity to survey the natural
enemies of the gypsy moth in different parts of the world and to introduce the
promising species in the United States. Information on such activities is
available in the reports of Drea (1978) in Europe, Iran and Japan; Drea and
Fuester (1979) in Poland; Gyorfi (1963) in Hungary; Hedlund and Mihalache
(1980) in Rumania; Herard and Fraval (1980) in Morocco; Herard, Mercadier
and Abai (1979) in Iran; Pschorn-Walcher (1974) in Europe; Rao (1966, 1972)
in India; Romanyk (1965) in Spain; Shapiro (1956) in Russia; and Vasic (1958)
in Bulgaria. Ina recent publication on the gypsy moth (Doane and McManus,
editors, 1981), Dr. Coulson has reviewed the introductions of the parasites
in the U.S.A. for the control of the gypsy moth.
In the United States, the states of New Jersey and Pennsylvania have
recently been active in the release of exotic parasites. According to the
publications of the Pennsylvania Bureau of Forestry, four species of Coccygo-
mimus were released in Pennsylvania during 1973-79, as follows.
Coccygomimus disparis, 73,215 ex stocks from India and Japan.
C. instigator 3,290 from Yugoslavia
C. turionellae 34, 134 from India
C. movraguesi 2,600 from Morocco
Of these only two specimens of C. disparis were recovered in July 1981
(Dr. Fusco, personal correspondence), which appears significant because
releases were made in 1979 or possibly in 1980, but not in 1981.
Phobocampe unicincta, which was established during 1911-1912 in the New
England states has also spread to New Jersey and Pennsylvania and it appears
that parasitism by this species is also increasing gradually in Pennsylvania
since 1970, particularly in post-climax gypsy moth populations. The native
pupal parasites were also active there in killing the host pupae.
The Ichneumonidae are either larval or pupal parasites of the gypsy moth.
The typical larval parasites are the members of the genera Phobocampe,
Casinaria and Hyposoter, belonging to the subfamily Porizontinae. They lay
their eggs within the young gypsy moth larvae and emerge from older larvae
and spin their own cocoons. Other internal parasites or endoparasites of the
larvae are the members of the subfamily Banchinae, Cremastinae and
Ophioninae. Members of the subfamily Anomalinae are endoparasites of the
V. Gupta: Gypsy Moth Parasites 3
larvae, but the emergence is from the host pupa. The external parasites of
the larvae or ectoparasites are the members of the subfamily Tryphoninae.
Members of the tribe Pimplini are external parasites of late larvae that have
just spun their cocoons or the prepupae and the development is upon host larva
within the cocoon. The Mesosteninae are apparently similar to the Pimplini in
their host relations.
Members of the tribe Gelini and of subfamily Mesochorinae are secondary
parasites of the various gypsy moth parasites, including Braconidae and
Ichneumonidae. Some genera are parasitic upon Tachinidae, particularly the
genera Mesoleptus and Phygadeuon. Species of Itoplectis and Theronia are
also hyperparasitic upon occasions.
The typical pupal parasites belong to the subfamily Ichneumoninae and the
tribes Ephialtini and Theroniini of the subfamily Pimplinae, e.g., the genera
Coccygomimus, Itoplectis, Ephialtes, and Theronia. They are internal para-
sites of exposed or semiexposed pupae. Oviposition is into the prepupa or
freshly formed pupa and the emergence of the adult parasite is from the host
pupa.
MATERIAL AND METHODS
The purpose of the present study was to establish the identities of the
various ichneumonid species that have been reported as parasites of the
gypsy moth. Over a hundred species of the Ichneumonidae have been recorded
as primary parasites and nearly 25 as secondary parasites. A near complete
list of the species and the various taxonomic combinations under which they
have been reported previously is given by Griffiths (1976). Previous useful
compilations are of Howard and Fiske (1911), Stadler (1933), Schedl (1936)
and Thompson (1946).
A literature search was made to establish the first records for each
species from the gypsy moth. This revealed that several erroneous records
had crept in the literature in the process of compilations. Many records have
never been confirmed by subsequent rearings and in such cases it was difficult
to assess the role of the parasite in the economy of the gypsy moth.
Attempts were made to gather specimens of Ichneumonidae that have been
reared in the past. Unfortunately voucher specimens do not exist for most of |
the earlier records. The only source from which such material could be
obtained was the Forest Insect Laboratory, Hamden, Connecticut, wherefrom
Specimens received and reared prior to 1930 were available.
In recent years several surveys have been made in Europe, Japan, India,
Iran and Morocco, to gather insect parasites of the gypsy moth, and to intro-
duce the promising species in the United States. Only a dozen or so species
of Ichneumonidae have usually been reared belonging to the subfamilies
Pimplinae and Porizontinae and one to the Ichneumoninae. Fortunately many
of these specimens were available for study. This helped tremendously to
establish the true identities of the species that are commonly encountered on
the gypsy moth. |
On the basis of these studies, 24 species of Ichneumonidae are confirmed
as parasites of the gypsy moth in the world (List I), 31 species are shown de-
finitely not to be associated with the gypsy moth (List III), and 38 species are
listed as unconfirmed records from the gypsy moth (List II). Some of these
may be occasional parasites, while some others appear to be misdetermina-
tions. Two new species or subspecies are described: Phobocampe lymantriae
from Lymantria dispar in Europe and Japan, and Theronia atalantae himalay-
4 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
ensis from Lymantria obfuscata from India. The taxonomic identity of all the
species has been updated.
The hyperparasites are listed in List IV. The hyperparasites were not
studied. Ichneumonid parasites reared in India from Lymantria obfuscata ,
a related species, are mentioned in List V. Many of these are being reared
in the U.S.A. for possible releases against the gypsy moth.
The institutions that loaned the species for the present study are listed
below, along with the names of the persons who arranged for the loans.
Bangalore, India Commonwealth Institute of Biological Control,
Indian Station, P.O. Box 2484, Bangalore, 560 024,
India. (T. Sankaran).
Newark, DE Beneficial Insects Research Laboratory,
501 S. Chapel St., Newark, Delaware, 19713.
(L. R. Ertle, R. W. Fuester, R. J. Dysart,
P. W. Schaefer).
Middletown, PA Division of Forest Pest Management, Bureau of
Forestry, 34 Airport Drive, Middletown, Pa. 17057.
(R. A. Fusco).
Washington, D.C. National Museum of Natural History, Smithsonian
Institution, Washington, D. C. 20560.
(A. S. Menke).
Trenton, NJ N.J. Dept. of Agriculture, Beneficial Insects
Laboratory, 101 Oakland St., Trenton, NJ 08618.
(R. Chianese).
EPL - Paris European Parasite Laboratory, USDA,c/o American
Embassy, AGR APO New York, NY 09777.
(B. D. Perkins).
Hamden, CT Forest Insect and Disease Laboratory, Forest
Service, USDA, 51 Mill Pond Road, Hamden, CT
06514 (W. E. Wallner).
In the lists and the text, that follows, the arrangement of the subfamilies
is in the order of their importance, and not taxonomic. Most species are
parasitic on several other lepidopterous pests besides the gypsy moth. The
list of alternative hosts is by no means complete. Thompson (1957), Aubert
(1967, 75), Townes et al. (1965) and Krombein et al. (1979) provide informa-
tion on the hosts of the various species of the Ichneumonidae. The nomencla-
ture of the lepidopterous pests has been updated after Lerut (1980).
ACKNOWLEDGMENTS
This research was funded by the U.S. Department of Agriculture. I am
thankful to Dr. Paul Marsh for processing the grant to work on the gypsy moth
parasites. I am grateful to Dr. Henry Townes for his constant help and advice
during the execution of this work. Drs. R. W. Carlson and J. R. Coulson
were very helpful in arranging for the loan of specimens from various sources.
They also provided valuable information on the parasite rearings, etc. My
thanks are also due to them, as well as to the persons listed above under loan
of specimens for sending me specimens for the present study.
I record my appreciation and thanks to Mr. L. E. Ling, who took the SEM
photographs for me.
V. Gupta: Gypsy Moth Parasites +)
LIST I
Ichneumonid species that are parasitic upon the gypsy moth and which have
been commonly reared from the pest. Specimens of these species have been
examined, reared from the gypsy moth.
i
12.
SUBFAMILY PIMPLINAE
Coccygomimus instigator (Fabricius) Page 23.
Pupal parasite in Eurasia, Iran and Morocco. Released in the U.S.A.
during 1906-1909 and again in 1972-79, but not established.
Coccygomimus pedalis (Cresson) Page 25.
Native North American parasite, stinging and killing a number of host
pupae, without successfully parasitizing them.
Coccygomimus turionellae (Linnaeus) Page 26.
(= Pimpla examinator Fabricius).
Pupal parasite, reared in Eurasia and India. Released several times
in the U.S.A., but not established.
Coccygomimus moraguesi (Schmiedeknecht) Page 28.
(= C, turionellae moraguesi?)
Apparently first reared from the gypsy moth pupae by Herard and Fravel
(1980) during 1973-75 in Morocco. Also occurring in Algeria and Spain.
Cultured and released in Pennsylvania during 1973-79 but not established.
Coccygomimus disparis (Viereck) Page 29.
(= Pimpla porthetriae Vier.)
A Japanese parasite of the gypsy moth, subsequently collected in India,
China, Mongolia and USSR. Released in Pennsylvania during 1973-79,
bred from stocks from India and Japan. Recently recovered there.
Coccygomimus luctuosus (Smith) Page 31.
(= misdetermination of Pimpla pluto and porthetriae in gypsy moth
literature).
A pupal parasite of the gypsy moth. Distributed in Japan and eastern
Asia.
Itoplectis conquisitor (Say) Page 35.
Native North American pupal parasite, stinging and killing a large
number of host pupae without successfully parasitizing them.
Itoplectis alternans alternans (Gravenhorst) Page 36.
Itoplectis maculator maculator (Fabricius) Page 37.
Itoplectis clavicornis (Thomson) Page 38.
Specimens of the first two species have been examined, labelled as
reared from the gypsy moth and also from its parasite Phobocampe
unicincta. ‘The third species is labelled as reared from Phobocampe
unicincta only. They occur in Europe. I. alternans spectabilis occurs
in Japan and is reported parasitic on the gypsy moth.
Ephialtes capulifeva (Kriechbaumer) Page 41.
Ephialtes compunctoy (Linnaeus) Page 42.
(= Pimpla brassicariae Poda)
Reared specimens of the above two species have been examined from
Europe and Japan. Vasic (1958) and Hedlund and Mihalache (1980)
reported having reared the latter species in Yugoslavia and Rumania,
respectively.
6 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
13. Theronia atalantae atalantae (Poda) Page 45.
14. T. atalaniae gestator (Thunberg) Page 48.
15. T. atalantae fulvescens (Cresson) Page 46.
Various subspecies of Theronia atalantae parasitize pupae of the gypsy
moth in Europe, Japan and North America. A related subspecies,
himalayensis, is described here as new from Lymantria obfuscata in
India. Sometimes T. alalantae is hyperparasitic.
16. Iseropus (Gregopimpla) himalayensis Page 55.
A reared specimen from Japan has been examined.
SUBFAMILY PORIZONTINAE
17. Casinaria tenuiventris (Gravenhorst) Page 63.
(= Campoplex conicus Ratzeburg)
Reared several times in Europe from the gypsy moth and also in Iran
in 1976. It has apparently not been seriously considered for introduc-
tion in the U.S.A. :
18. Casinaria nigripes (Gravenhorst) Page 64.
(= Casinaria anastomosis Uchida)
This species occurs in Europe and Japan and has been reared in small
numbers only.
19. Campoletis sp. Page 66.
Two reared specimens from France seen but the specific identity is
uncertain.
20. Phobocampe unicincia (Gravenhorst) Page 68. _
(= Hyposoter disparis Viereck = Phobocampe sp. of Herard et al.
from Iran).
A widespread species in Eurasia and already established in the U.S.A.
21. Phobocampe lymantriae Gupta Page 73.
(= Phobocampe n. sp. of Drea and Fuester, 1979, from Poland)
(= Hyposoter spp of Burgess and Crossman, 1929).
A species sympatric and similar to wnicincia, but biologically rather
different. Occurs in Europe and Japan. The majority of the specimens men-
tioned under "Hyposoter spp." by Burgess and Crossman belongs to this
species.
22. Hyposoter vierecki T. M. & T. Page 177.
(= Campoplex (Diadegma) japonicus Viereck)
Japan. Rearing records are rather few.
23. Hyposoter tricoloripes (Viereck) Page 178.
Reared several times in Europe in small numbers and apparently
released in North America, without success.
A related species, H. lymantriae occurs in India on Lymantria obfuscata.
This has been recently reared in large numbers at BIRL, Delaware on the
gypsy moth for possible release in the U.S.A.
SUBFAMILY ICHNEUMONINAE
24. Lymantrichneumon disparis (Poda) Pages 81, 87.
(= Ichneumon flavatorius = Trogus flavatorius).
A common but not abundant pupal parasite of the gypsy moth in Europe.
Also reported from Iran by Herard et al. (1979). Never reared in
V. Gupta: Gypsy Moth Parasites 7
large numbers for release in the U.S.A.
List II
Ichneumonid parasites that have been reported from the gypsy moth, but
the records of which could not be confirmed by examination of the reared
material. Some of them may be occasional parasites. The taxonomic
identity of quite a few species is doubtful.
SUBFAMILY PIMPLINAE
Coccygomimus spurius (Gravenhorst) Page 32.
Yafaeva (1959) recorded it from Ukraine. Aubert (1969) and Kasparyan
(1974) did not list it as a gypsy moth parasite.
"Coccygomimus sp." of Picard (1921) from France and of Herard and
Fraval (1980) from Morocco can be any one of the known species of
Coccygomimus. Identity doubtful.
Itoplectis alternans spectabilis (Matsumura) Page 37.
Reported by Fukaya (1936) from Japan. No subsequent confirmation.
Itoplectis viduata (Gravenhorst) Page 39.
Reported by Meyer (1929) from Russia.
Ephialtes rufatus (Gmelin) Page 438.
(= rujata Gravenhorst)
Reported by Rudow (1911) and Meyer (1927) from Germany and Russia
respectively. Not listed subsequently by Meyer (1934, 1936).
Theronia hilaris hilaris (Say) Page 50.
(= T. melanocephala). North America.
Earlier records of this species were considered to be misidentifications
of Theronia atalantae fulvescens. Campbell (1963) mentioned having
observed this species also on the gypsy moth, but did not discuss it
further. It may be an occasional parasite of the gypsy moth.
Acropimpla didyma (Gravenhorst) Page 5l,
Sedivy (1963) mentioned it from Czechoslovakia as Ephialtes didymus.
Iseropus (I1.) stercovator stercorator (Fabricius) Page 53.
(= Pimpla holmgreni)
Rudow (1911) reported it from Europe from Lymantria dispar and
L. monacha, but in 1917 listed only L. monacha as its host. There
are several such cases and his 1911 records appear rather doubtful.
Iseropus (Gregopimpla) inquisitor (Scopoli) Page 54.
Stadler (1933) apparently is the first to list it as a gypsy moth parasite
in Europe. Vasic (1958) reported it from Yugoslavia. No specimens,
however, could be examined to confirm its occurrence on the gypsy
moth. It may be an occasional parasite or a hyperparasite associated
with the gypsy moth. |
8 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
SUBFAMILY PORIZONTINAE
10. Campoplex difformis (Gmelin) Page 60.
(= ?Campoplex difformis Gravenhorst)
Species of Campoplex have often been misidentified in Europe and it
is doubtful what species, if any, is associated with the gypsy moth.
11. Campoplex sugiharai (Uchida) Page 61.
Momoi (1961) reported it from Japan as a parasite of the gypsy moth.
12. Phobocampe pulchella Thomson Page 67.
Shapiro (1956) reported it from Russia. Drea (in Doane and McManus,
1981: 317) mentioned it from Yugoslavia (determination by Vasic).
Apparently a misdetermination of either P. unicincta or P. lymantriae.
13. Hyposoter takagii (Matsumura) Page 76.
Fukaya (1950) first reported it from Japan. There are no subsequent
confirmations.
SUBFAMILY ICHNEUMONINAE
Almost all Ichneumoninae except Lymantrichneumon disparis (Poda)
have not been reared from the gypsy moth subsequent to their original records.
They have been merely catalogued subsequently, chiefly by Schedl (1936) and
Thompson (1946). Those cataloguers, however, missed several species
recorded from the gypsy moth by Rudow (1917, 1918).
Gyorfi (1963) mentioned Protichneumon rubens and P. fabricator, from
the gypsy moth, but the authenticity of these records cannot be confirmed.
Herard and Fraval (1980) mentioned having reared a species of Melanichneu-
mon (= Vulgichneumon) from Morocco. In the list that follows, the names
used in gypsy moth literature are given together with the original records.
Taxonomic details are given in the text.
14. Paracoelichneumon rubens (Fonscolombe) Page. 88.
(= Ichneumon = Protichneumon = "Ichneumon rubens Wesm. “
Rudow (1918). Europe.
15. Callajoppa cirrogaster cirrogaster (Schrank) Page 89.
(= Ichneumon lutorius F. = Trogus flavitorius lutorius F. = Trogus
lutorius F.) Howard and Fiske (1911). Europe.
16. Ichneumon cyaniventris Wesmael Page 91.
Rudow (1918). Europe.
17. Stenaoplus pictus (Gravenhorst) Page 94,
(="Ichneumon pictus Gmelin" of Stadler, Schedl and Thompson
= Stenichneumon pictus Gmelin of Thompson)
Mocsary (1885). Berthoumieu (1895) . Europe.
18. Melanichneumon leucocheilus (Wesmael) Page 95. Europe.
(= Ichneumon leucocheilus of Rudow, 1918 = 'Ichneumon leucocherrus "
of Stadler and Schedl, 1936, and I. leucocerus of Thompson, 1946).
= ?Melanichneumon (Vulgichneumon) sp. of Herard and Fraval, 1980
from Morocco ?
19. Cvatichneumon fabricator (Fabricius) Page 96.
(= Ichneumon = Protichneumon)
Cecconi (1924), Gy6drfi (1963). Europe.
20.
21.
22.
23.
24.
25.
26.
Bis
28.
29.
30.
se
V.
Chasmias paludator (Desvignes) Page 97.
(= Ichneumon = Chasmodes paludicola)
Rudow (1917). Europe.
Pterocormus sayrci
torius sarcitorius (Linnaeus) Page 98,
(= Ichneumon sarcitorius)
Meyer (1929). Russia.
Triptognathus amatorius (Mueller) Page 99.
(= Ichneumon = Amblyteles = Diphyus)
Rudow (1917), Uchida (1926). Japan, Sakhalin.
Spilichneumon occisor (Fabricius) Page 100.
(= Ichneumon = Amblyteles)
Rudow (1917). Europe.
Amblyteles armatorius (Forster) Page 102.
(= Amblyteles fasciatorius)
Uchida (1930). Japan.
Cotiheresiarches dirus (Wesmael) Page 104.
(= Eurylabus dirus)
Fahringer (1922)
. Europe.
SUBFAMILY MESOSTENINAE
Gambrus amoenus
(Gravenhorst) Page 106.
(= Cryptus, Aritranis, Spilocryptus)
= Gambrus nuncius (Say). N. America. N. syn.
Howard and Fisk
e (1911). Europe.
Meringopus cyanator (Gravenhorst) Page 108.
(= Cryptus, Trachysphyrus)
Howard and Fisk
Ischnus inquisitorius inquisitorius (Mueller) Page 109.
(= Ichneumon assertorius = Ischnus assertorius)
Rudow, (1917).
e (1911). Europe.
Europe.
SUBFAMILY TRYPHONINAE
Netelia (Netelia) vinulae (Scopoli) Page 111.
(= Panicus cepha
lotes)
Rtihl (1914). Europe.
Netelia (Netelia) sp. Page 111.
= ?Paniscus tes
taceus)
Ruhl (1914). Europe.
SUBFAMILY BANCHINAE
Banchus hastator (Fabricius) Page 113.
(= Banchus femoralis)
Kolubajiv (1934).
Europe.
Gupta: Gypsy Moth Parasites
10
32.
33.
34.
35.
36.
37.
38.
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
SUBFAMILY CREMASTINAE
Pristomerus vulnerator (Panzer) Page 115.
Barsacq (1913), Mokrzecki (1913). Europe.
SUBFAMILY ANOMALINAE
Trichomma (Trichomella) enecator (Rossi) Page 118.
(= Anomalon enecator)
Kirchner (1856). Europe.
Barylypa delictor (Thunberg) Page 120.
(= B. perspicillator)
Kovacevic (1925). Europe.
Barylypa pallida (Gravenhorst) Page 120.
(= Anomalon pallidum)
Rudow (1911). Europe.
Agrypon flaveolatum (Gravenhorst) Page 120.
(= Ophion, Anomalon)
Rudow (1911). Europe.
SUBFAMILY OPHIONINAE
"Ophion luteus (Linnaeus)"' Page 122.
Kolomiyetz (1958). Siberia. Identity of this species doubtful, as
O. luteus, has often been misidentified.
Enicospilus merdarius (Gravenhorst) Page 123.
(= Ophion)
Rtihl (1914). Europe.
Several other species recently collected in Morocco, Iran, etc., chiefly
by the staff of the European Parasite Laboratory, Paris, are mentioned in
reports as Ichneumonid sp. A, B, C, D, etc.
Dr. Lawrence R. Ertle (dated June 18, 1982), states, ''The Ichneumonids as
"A", "B", and 'C" were hyperparasites of Apanteles liparidis and A. melano-
scelus; Ichneumonids "D" and "'E" were not collected from L. dispar (L.),
but from Orgyia sp.”
LIST HI
Ichneumonid species that are definitely not associated with the gypsy moth.
Reasons for excluding them are given in details in the text.
SUBFAMILY PIMPLINAE
Perithous septemcinctorius (Thunberg) Page 16.
= Hybomischos. Parasitic upon Sphecidae rather than on Lepidoptera.
Dolichomitus tuberculatus (Fourcroy) Page 16.
Parasitic upon wood boring Coleoptera.
A recent letter from
10.
11.
12s
13.
14.
V. Gupta: Gypsy Moth Parasites 11
Exeristes roborator (Fabricius) Page 17.
(= Iseropus roborator)
Parasitic upon Ostrinia and related lepidopterous borers.
Coccygomimus aethiops (Curtis) Page 19.
Wrongly listed by Thompson (1946).
Coccygomimus pluto (Ashmead) Page 19.
Misdetermination of luctuosus Smith.
Coccygomimus tenuicornis (Cresson) Page 19.
Misdetermination of either C. pedalis or Itoplectis conquisitor.
SUBFAMILY PORIZONTINAE
Sinophorus validus (Cresson) Page 58.
Fusco and Simons (1977) listed it as a native gypsy moth parasite, but
correspondence with them failed to confirm its occurrence on the gypsy
moth. Not listed from the gypsy moth by Carlson (1979).
Campoplex difformis Gravenhorst Page 60.
Reported by Ratzeburg (1844). Its identity is uncertain and it was
almost certainly a misdetermination.
"Omorgus sp." of Kolomietz (1958) Page 59.
Reported as a parasite of the pupa of the gypsy moth. Appears to bea
misidentification.
Casinaria ischnogaster (Thomson) Page 62.
Morley and Rait-Smith erroneously reported it as a European parasite
of the gypsy moth.
Hyposoter fugitivus (Say) Page 17.
(= Limneria fugitiva, Limnerium sp.)
Erroneous record (Howard and Fiske, 1911).
Campoplex vapax Gravenhorst Pages 59, 75.
(= Anilastus = Anilasta)
Recorded by Rudow (1911). Its identity is very doubtful.
SUBFAMILY SCOLOBATINAE
Opheltes glaucopterous (Linnaeus) Page 124.
Record of its occurrence on the gypsy moth, originating from Rwthl
(1914) is erroneous, as members of the genus Opheltes are parasitic
upon Cimbex (saw-flies). Gyorfi (1963) mentioned it and several other
doubtful species from Hungary.
SUBFAMILY XORIDINAE
Xylonomus irrigator (Fabricius) Page 124,
Xovrides praecatorius (Fabricius) Page 124.
Rudow (1911) erroneously listed the above two species as gypsy moth
parasites. They belong to Xorides, which are parasites of wood boring
Coleopterous larvae. Morley (1908) also erroneously reported
Odontomerus dentipes as a parasite of Lymantria monacha .
12
26.
27.
28.
29.
30.
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
SUBFAMILY ICHNEUMONINAE |
Ichneumon vaptorius Gravenhorst Page 80.
Ichneumon sugillatorius Linnaeus Pages 80, 91.
Ichneumon melanoceras Ratzeburg Page 80.
These species were mentioned by Rudow (1911) as parasites of both
Lymantria dispar and L. monacha, but later (1918) only as parasites of
L. monacha. Many such records of Rudow (1911) appear erroneous for
the gypsy moth.
Ichneumon sp. Page 93.
Picard, 1921. Identity uncertain.
Ichneumon leucocerus (Gravenhorst) Page 92.
Thompson (1946). Misquotation of Ichneumon leucocheilus Wesmael.
Ichneumon leucocherrus" Wesmael Page 92.
Stadler (1933), Schedl (1936). Lapsus for I. leucocheilus Wesmael.
'Ichneumon pictus Gmelin'' Page 92. |
Stadler (1933). Identity of this species doubtful.
"Ichneumon flavus Rd."' Page 93.
(= Ischnus flavus Rd. of Stadler, 1933)
Rudow (1933) manuscript name. Nomen nudum.
‘“Amblyteles varipes Rudow" Page 103.
Rudow (1888). Identity doubtful.
Amblyteles camelinus Wesmael" Page 103.
Meyer (1936). Nota gypsy moth parasite.
SUBFAMILY MESOSTENINAE
"Ischnus flavus Rd.'' Page 105.
Stadler (1933). Europe.
Nomen nudum.
"Cryptus liparidis Rd.'' Page 105.
Rudow (1918). Stadler (1933). Nomen nudum. Subsequent authors
listed the author as ''Rond."'
SUBFAMILY GELINAE
Mesoleptus laevigatus (Gravenhorst)
(= Exolytus laevigatus)
Shapiro (1956). Russia.
A parasite of Diptera (mostly on Sarcophagidae) and not of Lepidoptera.
A related M. filicornis recorded erroneously on L. monacha.
SUBFAMILY TRYPHONINAE
"Paniscus melanurus Thomson" Pages 111, 112.
Meyer (1936) apparently confused it with testaceus. Identity uncertain.
'Paniscus testaceus Gravenhorst" Pages 110, 111.
What species was actually involved (Ruhl, 1914) is doubtful as testaceus
has been very often misidentified in the past. The true identity of it is
unknown.
V. Gupta: Gypsy Moth Parasites 13
SUBFAMILY BANCHINAE
31. Banchus falcatorius (Fabricius) Page 114.
(= Banchus falcator)
Morley (1915). Data as recorded by Morley indicate that it was never
reared from the gypsy moth, but collected flying where gypsy moth
larvae were also present.
LIST IV
Ichneumonid hyperparasites associated with the gypsy moth
SUBFAMILY MESOCHORINAE
Several species of Mesochorus, parasitic upon Apanteles species have
been associated with the gypsy moth, chiefly in Europe.
Mesochorus ater Ratzeburg. Europe.
M. confusus Holmgren. Europe, N. Africa.
M. discitergus (Say).
(= facialis Bridgman). Holarctic, Oriental.
M. dilutus Ratzeburg. Europe.
. dorsalis Holmgren. Europe.
. gracilis Brischke. Europe.
pallidus Brischke. Europe.
pectoralis Ratzeburg. Europe.
semirufus Holmgren. Europe.
splendidulus Gravenhorst. Europe.
sylvarum Curtis. Europe.
vitreus Walsh. N. America.
wh
SSSSS5888
SUBFAMILY GELINAE
—_
e
Acrolyta nigricapitata (Cook & Davis). N. America.
2. Atvactodes croceicornis Haliday (= A. compressus Thomson). Europe.
Parasite of Diptera. Might be secondary on Tachinidae associated.
with the gypsy moth.
Bathythrix triangularis (Cresson) (= Thysiotorus, Mesoleptus). North
America. )
3a. Dichogaster aestivalis Gravenhorst (= Hemiteles aestivalis). Incorrect
record. Parasitic upon Chrysopidae and not associated with Lymantria.
oo
Genus Gelis
(Many species reported under Pezomachus and some under Hemiteles .)
4. G, agilis Fabricius. Europe.
9. G. apantelis Cushman. U. S. A.
6. G. areator Panzer (= Hemiteles areator). Europe.
14 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
7. G. cinctus Linnaeus (= Hemiteles bicolorinus Grav.) Europe.
8. G. cushmani Carlson (= Hemiteles apanteles Cushman) U. S. A.
9. G. hortensis Gravenhorst (= Pezomachus) Europe.
10. G. instabilis Foerster (= Pezomachus) Europe.
11. G. intermedius Foerster. Europe.
12. G. inutilis Cushman. U.S. A.
13. G. nigriceps Foerster. Europe.
14. G. nigritus Foerster. Europe.
15. G. nocuus Cushman. U.S. A.
16. G. obscurus Cresson. U.S. A.
17. G. pulchellus Gravenhorst. Eurasia.
18. G. pulicarius Fabricius. Europe.
19. G. tenellus Say. U.S. A.
20. G. urbanus Brues (= Hemiteles cingulator Gravenhorst). Wrong record.
21. Lysibia nana. Gravenhorst (= Astomaspis nana, Hemiteles nanus,
Hemiteles fulvipes Grav.) Europe.
22. Mesoleptus filicornis Thomson (= Exolytus) Europe.
Parasitic on Tachinidae. May be on tachinid parasites of gypsy moth.
23. Phygadeuon subfuscus Cresson. U. S. A.
Parasitic on Sturmia scutellata.
Four other species of Phygadeuon have been reported in association
with Lymantria monacha, viz., P. flavimanus Grav., fumator Grav.
grandiceps Grav., and variabilis Gravenhorst. They are parasitic on
Tachinidae, perhaps associated with the nun-moth.
Species of the Pimpline genera Itoplectis and Theronia are also occasion-
ally hyperparasitic through other ichneumonids of the gypsy moth.
Euceros albomarginatus Cushman
Two males examined, bearing the following data:
"Eastern Pa., Summer 1976. Reared from Phobocampe cocoon from L. dis -
pay (Pennsylvania Bur. Forestry). E
LIST V
Ichneumonid parasites associated with Lymantria obfuscata Walker
Lymantria obfuscata occurs in India and its habits are similar to those of
L. dispar. The two were confused for a long time. Nagaraja et al. (1968) and
Rao (1972) showed that the two were different species.
The following ichneumonid parasites occur on Lymantria obfuscata in
India:
1. Coccygomimus turionellae (L.).
2. C. disparis (Viereck) (= Pimpla sp., turionellae Gr.)
3. C. laothoé (Cameron) (= poesia).
4. Theronia atalantae himalayensis Gupta (= Theronia sp., T. atalantae
atalantae).
5. Hyposoter lymantriae Cushman (= Anilastus sp., Hyposoter sp.).
Some of the above species have been reared on the gypsy moth in the
U.S.A. and also released in the field.
The identities of other ichneumonids reported by Rao (1966, 1972) have
not been established. These are ''Cryptinae gen. et sp. indet.'"', Cryptus sp.,
Metopiinae - Exochini "gen. et sp. indet.'’ and Goryphus sp. nr. inferus.
V. Gupta: Gypsy Moth Parasites 15
KEY TO THE SUBFAMILIES OF ICHNEUMONIDAE ASSOCIATED WITH
THE GYPSY MOTH
2. Clypeus and face forming a broad, weakly convex surface. Clypeus not
separated from face by a distinct groove. Areolet rhombic, large.
First tergite with a large glymma, its spiracles near middle. Male
claspers rod-like. Female subgenital plate large, triangular.
Brownish species, hyperparasitic within braconid cocoons.
(Mesochorus)/MESOCHORINAE
Not as above. Clypeus separated from face by a distinct groove except
in Porizontinae. Areolet various, never rhombic. ......... 3
3. Spiracle of first tergite placed behind the midlength of the tergite. First
tergite usually petiolate, slender at base. .........2.2e-ce0ee8 4
Spiracle of first tergite placed near midlength of the tergite. First
tergite usually quadrate to narrowly trapezoid, not slender at
PASO rie sae a BE ae ee ee ee Oe eae 10
4. Abdomen compressed laterally. Third and fourth segments deeper than
Oy i ei i dn ee Pe Tee oR Ae Oe es 5)
Abdomen'depressed or cylindric. Third and fourth segments wider than
DOOD 6s Sos aac wee bere eh ew OU ee re. 8
0. First intercubital vein (or the only intercubital vein present) joining
cubitus vein distad of second recurrent vein by a distance greater than
half its length. Epomia absent. Medium to large sized, pale brown
colored slender species with very compressed abdomen. (Ophion).
IX. OPHIONINAE
First intercubital vein joining cubitus basad of, opposite, or less than
half its length distad of second recurrent vein. .........s..e.e-. 6
6. Propodeum coarsely reticulated. Areolet absent. Hind tarsus often
swollen, especially in males. Slender species with long and much
COMPFeESGed abdomiene<¢ 25 sinks iw Bian wis VIII. ANOMALINAE
Propodeum not reticulated, with distinct carinae bounding separated
areas. Areolet present or absent. Hind tarsus not swollen. .... 7
7. Clypeus usually confluent with face. Face usually black. Ovipositor
straight or decurved. Hind femur not toothed below.
Il. PORIZONTINAE
Clypeus separated from face by a groove. Face usually pale. Ovipositor
sinuate and hind femur toothed below in the genus associated with the
gypsy moth. (Pristomerus). ........26.-. VII. CREMASTINAE
8. Ovipositor very short, hardly surpassing the tip of abdomen, its sheaths
always rigid. Notauli and sternaulus weak and short, or absent.
Clypeus broader, with its apex flat and truncate.
Til. ICHNEUMONINAE
16 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Ovipositor long to short, conspicuously extending beyond the tip of
abdomen. Notauli and sternaulus conspicuous. Ovipositor sheaths
USUALLY TIGR re ee eee se oe ee 9
9. Second recurrent vein with two bullae, sloping outwards. Propodeum
usually fully areolated. Face of male usually black. Hyperparasites.
GELINAE
Second recurrent vein with a single bulla, not sloping outwards. Propo-
deum with only transverse carinae, usually the basal transverse carina
BLONE PrOMinent. “4 ey Oe ee Ss IV. MESOSTENINAE
10. Tarsal claws not pectinate in females, sometimes with a large basal
tooth on some claws. Abdomen depressed. ..... I. PIMPLINAE
Tarsal claws pectinate. Abdomen compressed. .........eee-. tt
11. Prepectal carina present. Upper tooth of mandible a sharp point.
(NETO Te es eg ee er eee V. TRYPHONINAE
Prepectal carina absent. Upper tooth of mandible obliquely chisel-
Saved. S(PONChUis) To. ee a A ae SVL BANCHINAE
I. SUBFAMILY PIMPLINAE (= EPHIALTINAE)
Members of the subfamily Pimplinae are characterized by haying a
depressed abdomen, with first segment short, stout, broad, with its spiracle
at or in front of the middle. Glymma nearly always present. Apical margin
of clypeus usually thin and with a median notch. Mandible with two teeth.
Notauli weak or absent. Sternaulus absent or short and weak. Postpectal
carina incomplete. Propodeum usually not areolated (except Xanthopimpla,
Theronia and related genera). Tarsal claws never pectinate. Areolet usually
present and triangular. Nervellus intercepted variously. Abdominal tergites
usually with paired swellings. Ovipositor long, its tip without any notch, the
lower valve tip with ridges.
The larva of the Pimplinae differs from that of all other Ichneumonidae in
having the hypostomal spur and the stipital sclerite both well developed and
reaching each other at their apices, rather than the hypostomal spur reaching
the stipital sclerite before its apex. The larval antenna is usually well
developed and the mandible is with teeth, but in the tribe Ephialtini the antenna
is vestigial and the mandible is without teeth (cf. figures 123-132).
The adults are rather large and slender, with body and ovipositor elongate.
They are generally black in color (Coccygomimus, Itoplectis, Ephialtes,
etc.) or yellow to yellowish-brown (Theronia, Xanthopimpla).
Several species of Pimplinae are important parasites of the gypsy moth.
They are discussed below. The following species were erroneously recorded
as gypsy moth parasites, or their records are doubtful.
1. Perithous semptemcinctorius (Thunberg)
Griffiths (1976) reported this species as a parasite of Lymantria dispar
from Bulgaria, quoting Stefanov and Keremidchiev (1961). This species be-
longs to the genus Hybomischos, the species of which are parasitic upon
Sphecidae nesting in canes or twigs.
2. Dolichomitus tuberculatus (Fourcroy)
This species has often been recorded as a parasite of Lymantria monacha.
V. Gupta: Gypsy Moth Parasites 17
Members of the genus Dolichomitus are parasitic on wood boring Coleoptera,
and not on Lymantria. Dalla Torre (1902) cited L. monacha as a host, refer-
ring to Ratzeburg (1844), who however, mentioned "'Curculio pini" as a host
and not Lymantria. Also cited as Ephialtes tuberculatus by some authors.
3. Iseropus roborator (Fabricius)
Meyer (1936, pt. 6: 296-297) mentioned this species as a parasite of
Lymantria dispar and L. monacha. However, in his taxonomic treatment of
this species (1934, pt. 3: 22), the only host mentioned was Ostrinia nubilalis.
There is no subsequent record confirming its association with the gypsy moth.
This species properly belongs to the genus Exeristes and is widely distributed
in southern Europe and the Mediterranean area.
KEY TO THE TRIBES AND GENERA OF PIMPLINAE ASSOCIATED
| WITH THE GYPSY MOTH
1. Mesopleural suture straight, without a distinct angulation, the area
before it not depressed. When hind tibia banded, apical and basal dark
bands and a median pale band — the extreme base of tibia dark.
(Tribe Benin. (6 ag we Re Oe, ates are nie pee ie ee 2
Mesopleural suture with a weak angulation near middle. Mesopleural pit
area depressed. When hind tibia banded, there are apical and sub-
basal dark bands and median and basal pale bands—the extreme base of
igia thus pales tes ere a he ee Pie hte See ge, ee 8 4
2. Inner margin of eye weakly concave above antennal socket. Face of male
black. Tarsal claws of female without a basal tooth.
1. Coccygomimus (= Pimpla of authors)
Inner margin of eye rather strongly concave opposite antennal socket.
Face of male white, yellow or black. Fore tarsal claws of female with
A Aeere Haga TOG ig aa ee ak ee Oe ee gs 3
3. Ovipositor straight. Face and orbits of both sexes black. . 2. Itoplectis
Ovipositor hooked downwards at tip. Face of male largely or entirely
white or yellow. Orbits of female narrowly whitish in front.
3. Ephialtes
4. Tarsal claws of female, or at least the front claws, with a basal tooth.
Male subgenital plate wider than long. Body black or with black stripes.
Taye a a i i i be Te RO Ry ee ea wt eg ke 5
Tarsal claws of female without a basal tooth. Male subgenital plate longer
than wide. Body yellow or brownish-yellow. (Tribe Theroniini).
4. Theronia
5. Nervellus intercepted below the middle, rarely at middle. Ovipositor
sheath shorter than fore wing. First intercubitus of areolet shorter than
the second. Areolet wider than high, iriangular, and receiving second
recurrent vein at apical corner. Propodeum with short median carinae
ERGs hi RN RR el Ea? et EB eit ~«. oO Acropimpla
Nervellus intercepted at or above the middle. Ovipositor sheath as long
as or longer than fore wing. Areolet variable. ...... 6. Iseropus
18 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
6. Face of male white or yellow; clypeus of female usually red. Clypeus
weakly convex sub-basally, weakly depressed apically. Nervellus inter-
cepted near its upper 0.33. Ovipositor 0.5 as long as fore wing. Ocellar
triangle narrow. Interocellar distance a little less than ocellocular dis-
tance (0.8 to. 0.9:D)... . 6... 6s ee 6a. Iseropus (Iseropus)
Face of male and clypeus of female black. Clypeus strongly convex sub-
basally and depressed apically. Nervellus intercepted between its upper
0.4 and center. Ovipositor 0.6 to 0.8 as long as fore wing. Ocellar
triangle wider. Interocellar distance a little more than ocellocular dis-
tance (10:8). 2... i eke Bw ee 8 6b. Iseropus (Gregopimpla)
Tribe EPHIALTINI
Members of the tribe Ephialtini have the clypeus usually a little swollen
basally and flattened apically, mesoscutum without transverse wrinklings,
prepectal carina complete, mesopleural suture without an angulation near the
middle or sometimes with a weak angulation, propodeal carinae absent to more
or less complete (Xanthopimpla), propodeal spiracle elongate, areolet present,
nervellus intercepted usually above the middle, first tergite short, its lateral
carina usually strong, and ovipositor stout, long or short, with its tip a little
depressed.
The members of this tribe are common throughout the world. They are
usually internal parasites of exposed or semi-exposed pupae of Lepidoptera.
Species of Itoplectis are sometimes secondary parasites. Oviposition is into
the prepupa or pupa and the emergence is from the pupa. The host range of
an individual species is wide. The males are usually smaller than the females.
There is one parasite per pupa. They overwinter in the host pupa, or species
of Itoplectis sometimes overwinter as adults.
Three genera, Coccygomimus, Itoplectis and Ephialtes, are associated
with the gypsy moth, but only species of Cocensamanmss appear to be of some
importance in the control of the pest.
1. Genus COCCYGOMIMUS (Fig. 1)
_Coccygomimus Saussure, 1892. In Grandidier: Histoire Physique Naturelle
et Politique de Madagascar, 20 (Hyménopteres), Part 1, Pl. 14, Fig. 12.
This genus is often called erroneously as Pimpla by various authors. For
synonymical references, refer to Townes (1969). Townes and Townes (1960)
treated the Nearctic species, and Kasparyan (1974) reviewed the Palaearctic
species.
Moderately large-sized insects with fore wing 3.2 to 17.5 mm. long.
Antenna slender, thin and long. Inner margin of eye only weakly emarginate
above antennal socket. Malar space usually long. Mandibular teeth of almost
equal length. Notauli weak or absent. Propodeum and metapleurum usually
with coarse punctures and some striation. Median longitudinal carinae of pro-
podeum usually present basally. Tarsal claws large, simple, without a basal
tooth or an enlarged hair with a flattened tip. Abdomen usually closely punc-
tate (sometimes impunctate). Ovipositor straight, long and stout.
Members of the genus Coccygomimus are solitary, internal parasites of
prepupae and pupae of various Lepidoptera found beneath leaf litter. The
development is completed within the host pupa. They are polyphagous and
V. Gupta: Gypsy Moth Parasites 19
multivoltine. Some species overwinter within the host pupa. All species give
off a strong pungent odor when captured.
Various species of Coccygomimus have been recorded as parasites of
Lymantria dispar in Eurasia, Japan and North America. There have been many
misdeterminations in the past. The following species have been confirmed by
various authors as parasitic on the gypsy moth by rearings:
C. instigator (Fabricius). Eurasia.
C. pedalis (Cresson). North America.
C. turionellae (L.). Eurasia. Introduced in North America.
C. movaguesi (Schmiedeknecht). Morocco. Introduced in U.S.A.
Coccygomimus disparis (Viereck) (= C. porthetriae Viereck). Japan.
C. luctuosus (Smith). Japan. This species was misidentified by
Howard and Fiske (1911) as C. pluto.
Many of the above species are being cultured in the U.S.A. for fiela
releases. Metterhouse (in Doane and McManus, 1981: 363-365) provided some
biological information on these species.
Species of Coccygomimus that have been reported erroneously as parasites
of the gypsy moth are:
Oouohwh-e
1. Coccygomimus aethiops (Curtis) (= parnarae Viereck = aterrima
Gravenhorst). Europe.
Thompson (1946) listed this species as a parasite of the gypsy moth, citing
Stadler (1933) and Schedl (1936). These authors did not list this species. It
is also not listed as a parasite of the gypsy moth in the recent catalogs of
Oehlke (1967) and Aubert (1969).
C. aethiops is a rather distinct species, wholly black, closely, coarsely
punctate, and dull body sculpture. It belongs to the Turionellae Group and is
somewhat related to C. pluto and C. luctuosus.
2. Coccygomimus pluto (Ashmead). Japan
This species was reported as a parasite of Lymantria dispar by Howard and
Fiske (1911), who reared it from pupae received from Japan during 1908-1910.
I have seen a female with the data, "Ex. Porthetria dispar Linn., Japan, July
1908, Gip Moth Lab 1650", bearing a determination label, "Pimpla pluto
Ashm."' by Viereck. This is actually a specimen of Coccygomimus luctuosus
(Smith) which is very closely related to pluto. These two species have often
been confused in the past. C. pluto has not been subsequently reared nor men-
tioned as a parasite of the gypsy moth, except by cataloguers like Thompson
and Schedl, who based their information on Howard and Fiske. This species
should therefore be deleted from the list of the gypsy moth parasites.
Kasparyan (1974) provides a diagnostic key to separate the three very similar
looking species: parnarae = aethiops , pluto and luctuosus.
3. Coccygomimus tenuicornis (Cresson). Ll ee
Howard and Fiske (1911: 138) stated, '"Recorded as a parasite [of gypsy
moth] by Forbush and Fernald, but never reared at the Laboratory. Possibly
P. conquisitor was actually the species reared."
Thompson (1946), quoting Schedl (1936), reported it from Japan and U.S.A.
Simons et al. (1979: 31) have the following entry under C. tenuicornis
(Cresson):
20 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
"Riley and Howard (1894) reported occasional parasitism of the gypsy
moth. However, this was probably a misidentification of C. pedalis (Cresson)
or Itoplectis conquisitor (Say) (Carlson, 1978). "'
It is not a parasite of the gypsy moth.
4. Coccygomimus sp.
Picard (1921) reported this species from France. Its identity is uncertain
without Picard’s specimens. It can be any of the known European species of
Coccygomimus parasitizing the gypsy moth.
2. Coccygomimus sp.
Herard and Fraval (1980) reported this from pupae of the gypsy moth from
Morocco. Its identity uncertain.
The species of Coccygomimus that have been reported from other Lyman-
tria species are:
1. C. arcticus (Zett.) from L. monacha. Europe.
2. C. instigator (Fab.) from L. monacha. Europe.
3. C. contemplator (Mueller) from L. monacha. Europe.
Prior to 1932, specimens determined as contemplator were called
turionellae L. Several species have been mixed up under contemplator and it
is not certain whether true contemplator is parasitic upon Lymantria monacha.
4. "Pimpla dentata Thomson" from L. monacha. Europe.
Tragardh (1920) reported "Apechthis dentata Thomson" as a parasite of
Lymantria monacha for the first time from Sweden. Kolubajiv (1937) indicated
that 'dentata Thomson" was a lapsus for Pimpla quadridentata Thomson. This
species is now placed in Ephialtes.
5. C. turionellae (L.) from L. obfuscata. India.
6. C. disparis (Viereck) from L. obfuscata. India.
7. C. laothoé (Cameron) from L. obfuscata. India.
Rao (1966) mentioned two "Pimpla sp.''as parasites of pupae of L. obfus-
cata in Kashmir and Kotgarh. In 1972 he reported three species, C. turionellae,
C. sp. nr. turionellae, and C. laothoé from L. obfuscata. I have checked these
specimens. The specimens from Kashmir represent C. turionellae and
C. disparis (= C. sp. nr. turionellae of Rao). A female from Chimla, H. P.,
July 20, 1964, Kotgarh substation, det. as Pimpla poesia Cam. by Kerrich, is
C. laothoé (Cameron), C. poesia is a synonym of C, laothoé.
KEYS TO THE SPECIES OF COCCYGOMIMUS PARASITIC UPON THE
GYPSY MOTH PLUS THOSE OFTEN CONFUSED WITH THEM
Females
1. All legs, including their coxae, black. Eastern Palaearctic. Two species
OL AS PU PIO NOT Le CIP OUD eo te Wied ee Gilles eRe RL Mle lle bal wits 2
All legs not wholly black, either coxae or femora and tibiae red or
TO eae AAS i aici ark i i ned ote elec: cin oa oe 3
2. Body length 12-14 mm. Body pubescence brownish. Face with scattered
punctures, shiny in between. Mesopleurum with well separated shallow
V. Gupta: Gypsy Moth Parasites 21
punctures. Tergite 5 with shallow, not well formed punctures. Hind
coxa subpolished, mat. Propodeum punctate. Whole body more sub-
polished with shallower punctures. Japan (wrongly associated with the
sypsy Mot Ara Fee, Ta ee pluto (Ashmead)
Body length 15-20 mm. Body pubescence whitish or golden. Face strongly
punctate. Mesopleurum strongly punctate. Tergite 5 with coarse, well
formed punctures. Hind coxa punctate. Propodeum rugose to rugoso-
reticulate centrally. Whole body dull with coarse punctures. Japan.
6. luctuosus (Smith)
All legs including coxae, red. Scutellum red. Hind tibia with a distinct
white band, its basal half fuscous. Hind tarsus black. Mesopleural
punctation coarse. Morocco..... 4. moraguesi (Schmiedeknecht)
All coxae black or at least one pair of coxae black to blackish. Scutellum
black (sometimes: yellow tm taotho@) wii ws, coe 6 SAL baw er. 4
All coxae black. All femora reddish-brown or orange-brown. ..... 9)
Hind coxa reddish or yellowish-brown. Fore coxa black, or blackish-
brown. Middle coxa yellowish-brown or black. Femora reddish-
Body pubescence brownish. Hind tibia (and femur) wholly rufous, without
a white annulus. First tergite strongly to weakly pyramidal in profile.
Tegula black or yellow. Epipleura narrow. Fourth epipleurum about
3.0 as long as wide. (Instigator Group). Length 12to18mm.... 6
Body pubescence white. Hind tibia with a pale submedian band or wholly
black. First tergite short, not pyramidal in profile, without strong or
distinct humps. Epipleura wider. Fourth epipleurum the widest, about
2.5 as wide as long. (Turionellae Group). Length 9-15mm..... 7
Tegula black. Dorsal humps on tergite 1 prominent. Mesopleurum not
densely punctate, interspaces about 1.0 to 1.5 the diameter of punctures.
Eurasia, Japan, Iran, and Morocco. .... 1. instigator (Fabricius)
Tegula yellow to orange-brown. Dorsal humps on tergite 1 weaker. |
Mesopleurum densely punctate, punctures largely contiguous, or inter-
spaces less than the diameter of the punctures India, ex Lymantria
DOE hk 8! MEA eR A AE: laothoé (Cameron)
Hind tibia with a submedian pale band, or spot, or rarely wholly reddish.
Hind femur fuscous apically. Hind corner of pronotum yellow. Abdomen
with coalescing punctures, a little coarser than in disparis. Length
9-12 mm. Palaearctic and Oriental Regions.
3. turionellae (Linnaeus)
Hind tibia wholly black. Hind femur with a distinct black apical ring which
' may be as wide as 0.2-0.25 the length of femur. Hind corner of prono-
tum without yellow mark (only the postspiracular sclerite yellow). Abdo-
men punctate but not coarsely so, punctures rather well formed and
smaller. Length 12-15 mm. Japan and India. Introduced in U. S. A.
and possibly established in Pennsylvania. .... 5. disparis (Viereck)
Fore and middle coxae black or brownish-black. Hind coxa reddish or
yellowish-brown. (Parasites of Lymantria monacha). ........ 9
22
10.
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Fore coxa black or brownish-black. Middle and hind coxae orange or
yellowish-brown. (Parasites of Lymantria dispar). ......s.-. 10
Body 12-15 mm. long. Body pubescence brownish. Hind tibia brownish-
yellow, without any pale band. Propodeum trans-striate, with strong
basomedian carinae bounding a finely striate basal area. First tergite
with dorsal humps. Epipleura narrow. (Instigator Group). Europe.
arcticus (Zetterstedt)
Body 8-10 mm. long. Body pubescence white. Hind tibia with a sub-
median pale band. Propodeum with a smooth basal area bounded by
weak interrupted carinae. First tergite flat, without dorsal humps.
Epipleurae, particularly 4th and 5th, wide. (Aequalis Group). Europe.
contemplator (Mueller)
Body 12-18 mm. long. Pubescence brownish. Epipleura narrow. First
tergite conical, with dorsal humps. Hind tibia and tarsus black.
(Instigator Group). North America........ 2. pedalis (Cresson)
Body 8-10 mm. long. Pubescence whitish. Epipleura wide. First
tergite flat dorsally, without humps. Hind tibia and tarsus brownish,
with a faint suggestion of a submedian band on tibia. Hind tibia sometimes
rufous. (Aequalis Sub l Europe. .... 7%. spurius (Gravenhorst)
Males
All coxae red. Legs in general red. Hind tibia with a yellow subbasal
band. Hind tarsus black. Hind tibia sometimes a little fuscous.
seutellum red. Morocco: ... i... 4. moraguesi (Schmiedeknecht)
All coxae and legs never wholly red. Scutellum black or yellow marked.
2
All coxae wholly black. Body pubescence various. Tyloids present or
Middle coxae black or yellowish-brown. Hind coxa wholly or partly
yellowish-brown. Body pubescence brown. Tyloids absent. Hind
tibia. and tarsus Dlgck. eee Gee ee eh a es ee 9
PUG POU Diack oe a ee ee Bee ee 4
Ping TOM POs. fi ee ee ee Se eR. 5
Flagellar segments 6-9 with tyloids. Wing bases yellow. Scutellum with
a yellow spot. Body pubescence usually whitish, sometimes brownish.
Fore and middle tibiae and femora with yellow marks. Mesopleurum
coarsely punctate. Length 10-15 mm. Japan..... luctuosus (Smith)
Flagellar segments 6-7 (only) with tyloids. Wing bases black, though
tegula brown. Body pubescence white. Scutellum black. Fore femur
and tibia with brownish marks. Mesopleurum smoother. Length 8-10
Wit JOR Gor at Sue a ke 6. pluto (Ashmead)
Tyloids absent. Body small and slender, less than 10 mm. long. Hind
tibia with a distinct submedian white band. ..........2.2s6-. 6
V. Gupta: Gypsy Moth Parasites 23
Tyloids present on flagellar segments 6-7, 6-9 or 6-11. Body medium-
sized, over 10 mm. long. Hind tibia brownish, brownish-red, or black,
with of without a whitish band...) 0 ote ee Oe ee 7
6. Tergite 6 mat. Tegula whitish-yellow. Subapical band on hind tibia sharply
demarcated from the black tibia. Europe. ... contemplator (Mueller)
Tergite 6 coarsely punctate on front half. Tegula yellow, with a brown
spot. Subapical band on hind tibia with indistinct boundries. Hind tibia
brownish, -Buroper oe eo oo 6 ee 7. spurius (Gravenhorst)
7. Body pubescence brown. Tyloids present on flagellar segments 6-11.
Tegula black, or with a large yellow spot. Hind femur without any
apical black mark. Hind tibia brownish-red. Body 8-15 mm. long.
BUrasiae oe ees Pe eS Se 1. instigator (Fabricius)
Body pubescence whitish. Tyloids present on flagellar segments 6-7 only.
Tegula yellow. Hind femur black apically. Hind tibia brownish or
black, with or without a while bands 6. 64 ree OO 8
8. Hind corner of pronotum yellow. Hind tibia black and with a distinct
yellowish-white submedian band. Mesopleural sculpture smoother.
Length about 9-12 mm. Eurasia....... 3. turionellae (Linnaeus)
Hind corner of pronotum black. Hind tibia blackish or blackish-brown,
without a distinct yellow band. (Sometimes there is a faint suggestion
of a band). Mesopleural sculpture coarser. Length about 12-13 mm.
Japan and India. Introduced in U. S. A. and possiblv established in
POMNSVlVaNia se OS ORO ee 5. disparis (Viereck)
9. Middle and hind coxae yellowish-brown. Face comparatively smoother.
North America. 0 ear Per ee 2. pedalis (Cresson)
Middle coxa black. Hind coxa orange-brown dorsally and black ventrally.
Face more distinctly punctate. Europe. .... arcticus (Zetterstedt)
1. COCCYGOMIMUS INSTIGATOR (Fabricius) (Figs. 9, 15, 21, 27, 33)
Ichneumon instigator Fabricius, 1793. Entomologia Systematica, 2: 164.
Germany.
Pimpla instigator:Gravenhorst, 1818. Nov. Acta Physio Medica Acad.
Caesareae Leopoldino-Carolinae Nat. Curio, 9: 291.
Apechthis flavipes Matsumura, 1912. Thousand Insects of Japan, Suppl.
4: 144, Japan.
Coccygomimus instigator: Townes, Momoi and Townes, 1965. Mem.
Amer, Ent. Inst., 5: 51. China, Japan, Korea, Kuriles, Sakhalin,
Russia, and Europe. Several host records from Eurasia.
The earliest record of this parasite from the gypsy moth can be traced
to Rondani (1873) in Europe. Rudow (1911) mentioned it as a parasite of
Lymantria dispar, L. monacha, Euproctis similis and E. chrysorrhoea.
Carlson (1979) lists several synonyms.
Female: Face closely punctate, with a median ridge. Frons rather deeply
excavated, shiny, with minute punctures and a few trans-striations. Meso-
scutum somewhat shallowly punctate, shiny in between punctures. Scutellum
shiny, with a few scattered minute punctures. Mesopleurum with deep punc-
24 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
tures, tending to be punctato-striate along mesopleural suture. Punctures
not dense, separated by about 1.0 to 1.5 their diameter. Metapleurum rugoso-
striate in anterior half and distinctly striate posteriorly, including the promin-
ent submetapleural flattened ridge. Propodeum rugoso-reticulate to rugoso-
striate, without median carinae, apically shiny. First tergite pyramidal in
profile, with distinct dorsal humps, its apical half coarsely punctate, tending
to be rugose laterally. Second tergite coarsely punctate. Tergites 3-5 punctate,
punctures tending to be smaller progressively rearward, the following tergites
mat, subpolished. Hind coxa punctate. Tarsal claws broad, apically strongly
decurved. Fourth segment of fore tarsus strongly notched ventrally. Nervulus
slightly distad of basal vein. Epipleura 2 and 3 narrow. Fourth epipleurum a
little wider, rectangular, about 3.0 as long as wide.
Black. All coxae and trochanters black. All femora and tibiae orange-
brown, their tarsi brownish, with apical segments fuscous. Sometimes hind
tarsus wholly fuscous. Hind tibia without a pale band. Body pubescence
brownish. Tegula black.
Male: Similar to the female in sculpture and color, but with fuscous hind
tarsus, or hind tarsus often black. Tegula black or with a yellow spot.
Flagellum with tyloids on segments 6-9, 6-10, or 6-11.
Length: Male 8-15 mm. Female 15-18 mm. Fore wing 6-13 mm.
Specimens: 82, 4%, bred from gypsy moth at Melrose Highlands Lab.,
from pupae received from Hungary (Baja), July 1925; Austria, August 1907;
France, August 1910; Germany, August 1909; and Italy, August 1911 (Forest
Insect Laboratory, Hamden, Ct.). South Rumania, 1°, 1%, June 26-28, 1978,
ex Lymantria dispar, R. C. Hedlund. Poland 1%, August 1, 1975. Morocco,
North Kemitra, Mamora Forest, 1°, July 13, 1974, ex Lymantria dispar,
A. Fravel (all B.I.R.L., Newark, Delaware). 3°, 3%, bred at Trenton, N. J.,
from stock from Yugoslavia ex Lymantria dispar (N.J. Dept. Agriculture,
Trenton). Several European specimens seen in Townes collections (not
reared).
Distribution: Widespread in Eurasia and Japan. Also occurs in North
Africa. It has been reared from gypsy moth pupae in Iran and Morocco
(Herard et al., 1979, 1980).
Hosts: Several hosts have been recorded in Europe and Japan, for which
reference may be made to Townes et al. (1965) and Aubert (1969).
Coccygomimus instigator belong to the Instigator Group as defined by
Townes and Townes (1960). It is close to the Oriental C. laothoé (Cameron),
the European C. arcticus (Zetterstedt), and the Russian C. palmtiricus
(Kasparyan). In C. laothoé the mesopleural sculpture is denser and tegula
orange-brown to yellow. It is parasitic on Lymantria obfuscata. C. arcticus,
a parasite of Lymantria monacha, has smoother and shiny thorax, with meso-
scutum leathery, almost impunctate, and hind leg wholly orange-brown, with
its tarsus sometimes a little fuscous. The male has black coxae, but the
tyloids are absent. C. palmiricus is distinguished by its dark red hind femur,
narrower tarsal claws, which are apically less decurved, and fourth segment
of fore tarsus weakly notched ventrally.
Biological notes: Howard and Fiske (1911: 237) recorded that this species
was received in considerable numbers from Europe in shipments of brown tail
moth pupae during 1906 to 1909. During that time it was liberated in New
England states for control of the gypsy moth. It was, however, not recovered.
During 1973-79, 3,250 specimens of this species were released in Pennsylvania
from stocks from Yugoslavia. No recoveries have so far been reported.
Gyorfi (1963: 51) mentioned C. instigator as an important parasite of
Vv. Gupta: Gypsy Moth Parasites 25
Lymantria dispar in Hungary. Romanyk (1965: 34) mentioned that it has been
known as a gypsy moth parasite in Spain for a long time, but without having had
any great impact on the gypsy moth population there. The only exception noted
by him was its abundance during 1960-61, ina small gypsy moth infestation on
Minorca Island, where about 20% of the pupae were destroyed by this parasite.
Drea and Fuester (1979) reported that in Poland it was parasitizing 1.3 to 3.7%
of the pupae in 1975.
Howard and Fiske (1911) mentioned that its biology was similar to that of
C. pedalis and C. turionellae but that instigator had a tendency to hibernate
within the host pupa. They also mentioned its becoming hyperparasitic on
occasions on Iseropus coelebs (Walsh) [= Pimpla (Epiurus) inquisitoriella
D. T.]. It is a polyphagous, multivoltine species.
2. COCCYGOMIMUS PEDALIS (Cresson) (Figs. 11, 17, 23, 29, 35, 123)
Pimpla pedalis Cresson, 1865. Proc. Ent. Soc. Philadelphia, 4: 268.
Colorado, U. S. A.
Pimpla pedalis: Fernald, 1892. Bull. Hatch Exp. Sta. Mass. State Coll.,
19: 116. Massachusetts. Host: Lymantria dispar. Howard and
Fiske, 1911. U.S. Dept. Agr. Bur. Ent. Bull., 91: 137-138, 237-
239. Biol.
Coccygomimus pedalis: Townes, 1944-45. Mem. Amer. Ent. Soc.,
11: 62-63. Synonymical references. Host records.
This is a polyphagous parasite, first recorded from the gypsy moth in
the U. S. A. by Fernald (1892). Townes (1944-45) has given a full list of
hosts. Carlson (1979) provides further taxonomic and biological references.
It is one of the native North American parasites of the gypsy moth.
Female: Face dull-shiny, convex, with small, scattered punctures,
punctures denser close to antennal sockets. Frons excavated, subpolished,
without striations. Mesoscutum and mesopleurum shiny to subpolished, with
minute scattered punctures. Scutellum subpolished. Metapleurum shiny and
with weak oblique striations. Submetapleural projection narrow and much
less pronounced than in instigator. Propodeum leathery, punctate laterally
and trans-striate centrally. Sculpture much weaker than in instigator.
Median propodeal carinae faintly to distinctly visible in basal half and
diverging apically. Hind coxa impunctate. Nervulus slightly distad of basal
vein. First tergite somewhat conical, with dorsal humps, which are blunt.
Apical half of first tergite (except for its apical margin) with coalescing punc-
tures. Second, third and fourth tergites punctate. The following tergites
progressively less punctate to mat. Abdomen shiny between punctures. Epi-
pleura narrow, those of 4th and 5th tergites narrower than in the preceding
species.
Black. Body pubescence brown. Tegula black. Fore coxa black to
brownish-black. Fore leg otherwise yellowish-brown. Middle leg wholly
yellowish-brown. Hind coxa, trochanters, and femur yellowish-brown to
orange-brown. Hind tibia and tarsus wholly black, without any bands. Hind
femur fuscous apically.
Male: Similar to the female, but face more closely punctate. Frons with
scattered punctures. First tergite less conical. All legs yellowish-brown
with fore coxa yellowish apically and hind tibia and tarsus wholly black.
Flagellum without tyloids.
Length: 12-15mm. Fore wing 8-12 mm.
26 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Specimens: U.§.A.: Whiteford, Harford Co., Md., 1°, June 30, 1981,
ex pupa of Lymantria dispar, R. Tateman (BIRL, Newark, Delaware). Winters
State Park, Pa, 1%, ex L. dispar, July 17, 1975 (Delaware). Schuylkill Co.,
Tremont Township, Pa. 1°, 1°, July 4, 1974 (Bureau of Forestry, Pennsyl-
vania). North Saugus, Mass., 1°, ex Lymantria dispar, Gypsy Moth Lab.
(F.1I.S., Hamden).
Distributien:: Common in Transition and Canadian zones in North America.
Coccygomimus pedalis belongs to the Instigator Group and is readily dis-
tinguished from C. instigator by its smoother thorax, and impunctate hind coxa.
It is related to C. arcticus in having brown body pubescence, red hind coxae and
by the absence of tyloids on the male flagellum. The general body sculpture
of the two is also similar, but avcticus has a more striate propodeum. In
pedalis, the middle coxae are yellowish-brown and face smoother, while in
arcticus, the middle coxae are black and face comparatively more punctate.
The two may be considered subspecies (Townes, 1940).
Coccygomimus pedalis is a polyphagous multivoltine species, overwintering
within the prepupa in the host pupa. It is one of the native prepupal or pupal
parasites of the gypsy moth, but parasitism is not common. It is therefore not
considered important. There are two to three generations per year. It takes
about three weeks to complete its development within the host pupa. It attacks
several other hosts (Townes, 1945; Carlson, 1979). Campbell (1963) observed
it attacking gypsy moth pupae and prepupae in Glenville, New York State. He
found that although parasitism was scarce, it killed more pupae and prepupae
through stinging than those successfully parasitized. These stung pupae and
prepupae were subsequently infested by sarcophagid larvae which acted as
scavengers. He observed that pedalis was common in the field and exerted a
great influence on the population of the gypsy moth by killing the prepupae and
pupae rather than by successfully parasitizing them.
3. COCCYGOMIMUS TURIONELLAE (Linnaeus) (Figs. 7, 13,19, 25, 31, 124)
Ichneumon turionellae Linnaeus, 1758. Systema Naturae, 10: 1: 564.
Europe.
Pimpla turioneliae: Gravenhorst, 1818. Nova Acta Physico Medica Akad.
Caesareae Leopoldino-Carolinae Nat. Curio, 9: 291.
Cryptus examinatory Fabricius, 1804. Systema Piezatorum, p. 85.
Austria.
Pimpla examinator: Ratzeburg, 1844. Die Ichneumonen der Forstinsecten,
1: 116. Germany. Hosts: L. monacha and others.
Caccygomimus turionellae: Townes and Townes, 1960. U.S. Natl. Mus.
Bull. , 216(2): 323. Synonymy and other references.
This species has often been referred to as Pimpla examinator in gypsy
moth literature. Howard and Fiske (1911) mentioned having reared it in the
laboratory from both the gypsy moth (Lymantria dispar) and the brown tail
moth (Euproctis chrysorrhoea). It was received in the U. S. A. in consider-
able numbers in shipments of brown tail moth pupae from Europe and was
released in the field during 1906-1909, but not recovered.
Carlson (1979) provides further biological references. Aubert (1969) and
Oehlke (1967: 32) give all synonymical references.
Male and female: Male flagellum with tyloids on segments 6 and 7. Face
largely rugulose to ruguloso-punctate, convex, more so inthe male. Frons
excavated, punctato-striate. Interocellar distance 1.5-1.8 the ocellocular
V. Gupta: Gypsy Moth Parasites 27
distance. Ocellocular distance about half the ocellar diameter. Ocellar area
smoother. Mesoscutum punctate. Punctures dense, small, but not coarse,
areas between them subpolished. Scutellum flat to subconvex, punctures sparse.
Scutellum punctate. Mesopleurum punctate, punctures coarser than on meso-
scutum, well separated with interspaces shiny, on lower half with well separ-
ated but larger punctures. Metapleurum finely punctato-striate, the striations
extending over flattened and expanded submetapleural ridge. Propodeum con-
vex, rugoso-striate on basal half, without any median carinae, except rarely
at base. Extreme base of propodeum in the middle, and apical half of propo-
deum polished to subpolished, the basal smooth area often depressed. Hind
coxa punctate. Nervulus interstitial. First tergite short and wide, convex in
profile with weak humps, not conically produced medially. Postpetiole largely
shiny with scattered punctures. Abdominal tergites 2 to 4 closely punctate,
with shiny interspaces. Apical tergites finely punctate to mat. Apical margins
of tergites shiny. Epipleura of tergites 1-3 narrow, of tergites 4-5 wider,
that of 4th the widest.
Black. Body pubescence white. Tegula and hind corner of pronotum
yellow. All coxae black, trochanters blackish-brown, and femora reddish-
brown. Fore and middle tibiae and tarsi yellowish-brown, with tibiae fuscous
dorsally and with a pale band or streak. In male tibiae and tarsi paler. Hind
tibia black and with a distinct yellow submedian band. Hind tarsus black.
Hind femur fuscous apically. Some males from USSR have the hind tibia
wholly reddish. Sometimes apices of abdominal tergites, particularly in males,
brownish.
Length: 9-12 mm. Fore wing 7.5 to 10 mm.
Specimens: Germany, 1°, bred from Lymantria dispar at Gypsy Moth
Lab., Sept. 30, 1907 (Hamden). S. Rumania: 2°, ex Lymantria dispar,
EPL-78-71, June 26-28, 1978, R. C. Hedlund (BIRL, Newark). 2°, 99,
reared at Trenton, N.J. ex Lymantria dispar, 1973-1975, presumably from
stocks from India (BIRL, Delaware), 2° (Bureau of Forestry, PA). Imported
in the U.S.A. from India and Rumania (cf. computer printout of BIRL, Dela-
ware). India: Kashmir: Srinagar, 1%, 19, July, 1964, ex Lymantria obfus-
cata (CIBC, Bangalore). Several males and females from Europe (Townes).
Coccygomimus turionellae resembles superficially C. instigator, from
which it can be readily distinguished by its white pubescence and black hind
tibia having a yellowish-white annulus. It is a comparatively smaller sized
Species with finer body sculpture. It has wide fourth and fifth epipleura
(Turionellae Group).
Distribution: Widely distributed in the Palaearctic and Oriental Regions.
Imported into North America several times during 1906 to 1979 from Europe
and India. Apparently not established. Recent rearing records from the gypsy
moth are by Vasic (1958), Yugoslavia; Rao (1972), India; and Hedlund and
Mihalache (1980), Rumania.
Hosts: Several hosts are known in Europe, USSR and Japan (Townes,
Momoi and Townes, 1965), Sedivy (1963). It is a polyphagous parasite of
Lepidoptera and Coleoptera.
Biological Notes: Several thousand specimens of this species were
released against the gypsy moth in Pennsylvania during 1973-79, bred in the
laboratory from specimens of Indian origin. According to Pennsylvania Bureau
of Forestry Report (? 1979), it was not recovered during subsequent years.
Carlson (1979: 346) provides a historical record of its introductions in
Eastern North America and Canada during 1906-1955. The target hosts in
North America were introduced pests, like Lymantria dispar, Rhyacionia
28 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
buoliana, Cydia (Cydia) pomonella and Operophtera brumata. A number of
native pests were target hosts also for some of the introductions. Establish-
ment has apparently not occurred, although a few recoveries have been reported
in Ontario, Canada.
Rao (1966) provides some information on the life history of this species
under 'Pimpla sp.'' reared in Kashmir, India, from pupae of Lymantria
obfuscata. Two generations were observed in Kashmir. The adults of the
first generation appeared in early May and those of the second generation in
late June. Mating occurred readily between freshly emerged males and older
females, lasting 35 seconds to one minute. Pre-oviposition period is 3-4 days.
Oviposition is in freshly formed pupae and takes two to two-and-a half minutes.
Generally a single egg is laid ata time. The egg measures 2.0 x 0.35 mm.,
‘ and is round at one end and tapering at the other. Soon after oviposition the
female feeds upon the oozing fluid from the puncture. The egg hatches in about
2 days. Larval period is 9-11 days. The first larval instar is 2.5 mm., and
the fully grown larva is 7-13 mm. long. Pupation occurs inside the host pupa.
The pupal period is 7-8 days. The adult males and females lived in the labora-
tory for about 25 and 40 days, respectively. The ratio of males to females
was 1: 3. Only one parasite develops per host.
Metterhouse (in Doane and McManus, 1981) has also provided biological
information on this species apparently based upon his observations during
culturing it in the laboratory. His data differ only slightly from what has been
given by Rao from field studies. The biology of C. disparis, instigator and
movraguesi is Similar to that of turionellae.
In the field collected pupae of the gypsy moth, the larvae and pupae of
Monodontomerus sp. were seen with the remains of 'Pimpla sp" larvae.
Rao (1972) reported three species of Coccygomimus from Lymantria
obfuscata in Kashmir and Kotgarh, India. These three species, confirmed
after examining the specimens, are C. turionellae, C. disparis and C. laothoé.
He reported that the aggregate parasitism by the three species was generally
low in all the four localities studied in Kashmir. The percentage parasitism
was 0.45 to 12.58% in 1968-69 and 1.36% in 1971. However, in 1970, the
parasitism was reported to be 17.35 to 67.41 percent.
4. COCCYGOMIMUS MORAGUESI (Schmiedeknecht) (Figs. 8, 14, 20, 26, 32)
Pimpla Movraguesi Schmiedeknecht, 1888. Zool. Jahrb., 3: 479. Morocco.
Coccygomimus turionellae moraguesi: Oehlke, 1967. Hymenopterorum
Catalogus, 2(1): 32.
Coccygomimus moraguesi has usually been referred to as C. turionellae
moraguesi in gypsy moth literature in the U. S. A. It is mentioned in the
reports of the Pennsylvania Bureau of Forestry, among the 15 exotic parasites
that were released against the gypsy moth in Pennsylvania since 1973. Carlson
(1979) states that Pimple freyt Héllen from the Canary Islands is probably a
synonym of it. Both movaguesi and freyi were treated by Aubert (1969) as
synonyms of turionellae.
Simons ef al. (1979) differentiated C. turionellae moraguesi from
C. turionellae turionellae by stating that the former species has hind coxa
and disc of scutellum reddish, while the latter species has both these structures
black. Both taxa have a yellow or yellowish-white sub-basal band on hind tibia.
I find that the body sculpture of movaguesi is coarser than that of turionellae,
justifying separation as a species.
V. Gupta: Gypsy Moth Parasites 29
Male and female: Essentially similar and related to C. turionellae and
differing as follows: Face distinctly punctate. Punctures coarse, tending to
run into striations near antennal sockets. Face with a median smooth
raised ridge in female and a convex median punctate area inmale. Frons exca-
vated, largely striate and punctate laterally. Ocelli larger than in turionellae,
closer to the eye. Interocellar distance 2.0 to 2.3 the ocellocular distance.
Ocellocular distance 0.3 the ocellar diameter. Thorax closely and coarsely
punctate, with scutellum convex and smoother, sometimes with minute
scattered punctures. Mesopleural punctures rather coarse and close together.
Metapleurum coarsely punctato-striate, sometimes tending to be rugoso-
striate infemale. Propodeum rugoso-striate with short median carinae at
base. Abdomen coarsely punctate. Postpetiole densely punctate.
Black. Tegula and hind corner of pronotum yellow. Tegula of female
often black on apical half. Scutellum, metascutellum and all legs reddish.
Fore and middle tibiae with light fuscous marks. Hind tibia with fuscous
basal and apical marks and a sub-basal yellow band. Hind tibia fuscous.
Often middle tibia also with a yellow subbasal band. Fore tibia and tarsus
sometimes with yellow lines, or tibia largely yellow in male. Abdominal ter-
gites with reddish-brown margins.
Length: 9-13 mm. Fore wing 6-9 mm.
Specimens: Algeria, 1°, bred from Lymantria dispar at Gypsy Moth
Laboratory, No. 13029 (Hamden, Ct.) [det. as Ephialtes sp. by Muesebeck].
Morocco: North Kemitra, Mamora Forest, 19, July 13, 1974 A. Fraval, ex
live shipment of Lymantria dispar. 1° 59, "Lab culture, Trenton, N. J."
(BIRL, Delaware). 2° "Parasite Lab, Middletown, Pa." (Pennsylvania) and
5c, 2 (Trenton, N. J.).. A computer printout received from BIRL, Delaware,
indicates importation of this parasite in the U. S. A. from Morocco during
1976-77.
Biological notes: Coccygomimus movraguesi is a polyphagous multivoltine
parasite of pupae of various Lepidoptera (as are other Coccygomimus). It is
known from North Africa: Algeria and Morocco. Seyrig (1927) recorded it
from Spain from Malacosoma neustria. Its biology is similar to that of
C. turionellae.
A specimen from Algeria bred from Lymantria dispar at the Gypsy Moth
Laboratory in Massachusetts prior to 1930, has been seen. It had remained
unnoticed due to lack of specific identification. Only recently this species
was introduced in the U. S. A. from Morocco and bred in the laboratory for
field releases. According to Pennsylvania Bureau of Forestry Report, 5, 600
specimens of it were released against the gypsy moth in Pennsylvania during
1973-79, but it has not established itself there.
5. COCCYGOMIMUS DISPARIS (Viereck) (Figs. 10,16, 22,28, 34)
Pimpla (Pimpla) disparis Viereck, 1911. Proc. U. S. Natl. Mus., 40: 480.
Japan. Host: Lymantria dispar.
Pimpla (Pimpla) porthetriae Viereck, 1911. Proc. U. S. Natl. Mus.,
40: 480. Japan. Host: Lymantria dispar.
Coccygomimus disparis: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 48. Japan, Korea, China, Sakhalin.
Several taxonomical and biological references to this species are listed in
Townes ef al. (1965). Kasparyan (1974) records it from Mongolia, China, and
USSR.
30 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Male and female: Face closely punctate, punctures of moderate size and
more regularly disposed. In female a smooth median raised area below antennal
sockets. Male flagellum with tyloids on flagellar segments 6-7. Tyloid on 6th
segment smaller. Frons excavated, faintly rugoso-striate. Mesoscutum with
well separated punctures, interspaces shiny. Mesopleurum also with well
separated punctures, but deeper than on mesoscutum, interspaces shiny.
Scutellum a little elongate, laterally margined and punctate. Metapleurum
rugoso-striate. Submetapleural ridge thinner, narrower and weakly striate.
Propodeum rugose, with a few irregular striations centrally and smoother
apically. Median carinae present basally or obliterated. When carinae
present, the area in between them smooth. Hind coxa shallowly punctate.
Nervulus interstitial. First tergite wide and flat apically, without dorsal
humps, though medially convex in the female. Postpetiole densely punctate,
smoother medially. Tergites 2-4 densely punctate, puntures coalescing. Ter-
gite 5 onwards basally punctate and smoother apically, the punctures progres-
sively becoming smaller to mat. Epipleura of tergites 4-5 wider than those of
tergites 1-3, the fourth widest.
Black. Tegula yellow, often apically black marked. Postspiracular
sclerite alone yellow near hind corner of pronotum. All coxae and trochanters
black. All femora reddish-yellow. Hind femur black in apical 0.2 to 0.25.
Fore and middle tibiae and tarsi yellowish-brown to orange, with faint fuscous
marks on tibiae. Hind tibia and tarsus wholly black or blackish. Body pubes-
cence white. : Q
Length: 12-15mm. Fore wing 10-12 mm.
Specimens: Japan, 1%, 22 (paratypes, Nos. 13078), ''Gipsy Moth Lab."
(Washington). 1°, Gypsy Moth Lab, No. 3309B. 1%, Gifu, Japan, Y. Nawa
Coll. (Washington). Japan, 1%, ex L. dispar, Gipsy Moth Lab, No. 1650
(Hamden). Nishigahara, Japan, bred from L. dispar (labelled Paratype of
P. disparis Vier.) (Hamden). Japan: Nara, Honshu, 1¢, ex Pupa, Lymantria
dispar, June 23, 1977, P. Schaefer, emerged July 7, 1977 BIRL, (Newark).
1c, 2°, Lab reared in New Jersey Dept. of Agriculture from stocks from India
(Pennsylvania) and 1% (Trenton). India: Srinagar, Kashmir, ex Lymantria
obfuscata on Willow, July 1963 (CIBC, Bangalore).
Distribution: Japan, Korea, China, Sakhalin, Mongolia, and India.
Hosts: Several host records, besides Lymantria dispar, are listed in
references given in Townes ef al. (1965) and Kasparyan (1974).
Coccygomimus disparis belongs to the Turionellae Group and is close to
C. turionellae in the nature of pubescence, epipleura and general body sculpture.
It differs from turionellae and moraguesi in having the hind tibia wholly black,
without a white or yellow subbasal band, hind corner of pronotum not yellow
(except for the postspiracular sclerite), tegula yellow, hind femur black in
apical 0.3+ 0.05, and abdominal punctures well formed but not coarse. It is
comparatively larger in size. The tyloid on the 6th segment of the flagellum of
the male is smaller. The scutellum also appears distinctive.
Coccygomimus indra (Cameron) from India, belonging to the Instigator
Group, has similar coloration of the legs, but the abdomen has sparse punctures,
particularly on the second tergite.
Coccygomimus nigricoxata Oehlke from Europe and USSR is also close to
disparis, but differs in having coarser punctation on abdominal tergites with
margins of punctures indistinct, especially on the apical half of fourth and
whole of the fifth tergite. The interspaces between the punctures are mat, with
indistinct fine sculpture. The hind femur is brownish or red with darker apex.
Biological notes: Although this parasite was received in the U.S.A. during
V. Gupta: Gypsy Moth Parasites ; Si
the first decade of the century, it has never been given serious attention
because of the scanty material that was received. During 1973-79, this species
was bred at the New Jersey Department of Agriculture, Trenton,from stocks
from India and also bred and released in Pennsylvania by the Pennsylvania
Bureau of Forestry. In one of their reports, it is stated that 73,215 speci-
mens were released from stocks from Japan and India, but that it was never
recovered except in the year of release. Metterhouse (in Doane and McManus,
1981), mentions that 10 specimens of this species were recovered in N. J.
during 1978, but that the species is not yet known to be established in North
America.
A recent letter from Dr. Fusco (Jan. 19, 1982) indicates that it was
recovered in Bradford County, Pennsylvania, near Towanda on July 13, 1981.
Two males of this species emerged from Lymantria dispar pupae collected
there. No releases of C. disparis were made in 1979 or 1980 in that county.
The closest release site was about 30 miles away in an adjacent county. The
New York state border is rather close, where C, disparis was released in
1979 and possibly 1980, but not in 1981.
Rao (1966, 1972) gave some biological information on three Coccygomimus
species, including the present species (see under turionellae).
6. COCCYGOMIMUS LUC TUOSUS (Smith)
Pimpla luctuosa Smith, 1874. Trans. Ent. Soc. London, 1874: 394.
Japan.
Coccygomimus luctuosus: Townes, Momoi and Townes, 1965. Mem.
Amer. Ent. Inst., 5: 53.
For full synonymical references, distributional records and host records |
(up to 1964) refer to Townes et al.(1965). Kasparyan (1974) provides a key to
distinguish it from the Eurasian species.
This species is widespread in Japan, and Asian USSR and has also been
reported from Korea, Taiwan, Sakhalin, etc. It has often been confused with
C, pluto and C. porthetriae in the Japanese literature. Uchida (1930) and
Matsumura (1931) reported it from Lymantria dispar (as porthetriae) in Japan.
Yasumatsu and Watanabe (1964) include it in their list of parasites of the gypsy
moth in Japan.
A female bred by Howard and Fiske (1911) in 1908 from pupae sent from
Japan and determined as pluto by Viereck, actually belongs to this species,
confirming the occurrence of this parasite on the gypsy moth.
Male and female: Face punctate. Punctures coarser and running into
striations below antennal sockets. Face with a median smooth area. Face of
male more regularly punctate and convex. Flagellar segments 6 to 11 in the
male with tyloids. Mesoscutum punctate, punctures a little smaller and
shallower than on mesopleurum. Scutellum flat to subconvex and shiny,
with scattered punctures. Mesopleurum strongly punctate, but punctures not
coarse or alveolar (as in aethiops), interspaces shiny and equal to the diameter
of punctures. Punctures sometimes closer or contiguous at places. Metapleu-
rum rugoso-striate anterodorsally and striate posteroventrally. Striations
extending on the expanded and rather wide submetapleural ridge. Mesopleural
suture below the mesopleural pit with well separated 10-13 transverse ridges.
Propodeum rugose to rugoso-reticulate, its extreme base with two small
median carinae, its apical region not smooth. First tergite sharply angled
medially, with two small humps. Postpetiole and second and third tergites
32 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
rather coarsely punctate. Central part of fifth tergite with well formed punc-
‘tures. Apices of all tergites smooth and shiny. Hind coxa punctate. Fourth
segment of fore tarsus deeply notched apically. Nervulus interstitial or a little
distad of basal vein. Male with first tergite flatter and thoracic sculpture a
little weaker. Smaller sized specimens with weaker sculpture.
Black. Body pubescence whitish or light brown. Wing bases and their
sclerites yellow. Tegula black or brownish-black. Legs black. Fore tibia
yellowish anteriorly. Sometimes fore and middle femora yellow apically and
their tibiae and tarsi brownish to brownish black. Hind tibia sometimes with a
faint suggestion of sub-basal light colored spot or band. In male scutellum with
a yellow spot. Tegula yellow with a black apical spot. Fore and middle femora,
tibiae and tarsi often partly to largely reddish-brown to yellowish-brown.
Length: 15-20 mm. Fore wing 11-14mm. Sometimes the male smaller.
Specimens: Japan: 12, July 1908, Gypsy Moth Lab., No. 1650, ex
Lymantria dispar, det. by Viereck as ''Pimpla pluto Ashm."' (Hamden).
Japan: Sapporo, 12 (homotype of Pimpla luctuosa by Townes), T. Uchida
(Townes). Japan: Yokohama, 1° (homotype of Pimpla aethiops neustriae
Uchida by Townes), May 20, 1933 (Townes). In addition, a few males and
females from Fukien, China and Japan seen in the Townes collection.
Distribution: Japan, Korea, China, Sakhalin, and Eastern USSR.
This species is related to Coccygomimus pluto (Ashmead) and C. aethiops
(Curtis). C. aethiops has densely punctate abdominal tergites and mesopleu-
rum, the punctures on mesopleurum touching each other and becoming alveolar.
The body is dull. The first tergite is without dorsal humps. The fourth tarsal
segment of fore leg is bilobed, but not deeply notched. C. pluto differs from
luctuosus in having the wing bases and tegula black. The scutellum of male is
black. Only 6-7th flagellar segments in the male have tyloids. The body
sculpture is a little sparser, with punctures on face less dense, on mesopleu-
rum well separated, shallower, and on tergite 5 not well formed and shallow.
It is also smaller in size, about 12-14 mm. long and with brownish-black
pubescence, though in male the pubescence is yellowish.
7. COCCYGOMIMUS SPURIUS (Gravenhorst) (Fig. 125)
Pimpla spuria Gravenhorst, 1829. Ichneumonologia Europaea, 3: 179.
Europe.
Pimpla spuria; Yafaeva, 1959. Ukrainskaya Akad. Selsk. Nauk, p. 227.
Ukranian SSR. Host: Lymantria dispar.
Coccygomimus spurius: Townes and Townes, 1960. Bull. U. S. Natl. Mus.,
216(2): 338.
Coccygomimus spurius has only recently been recorded as a parasite of
the gypsy moth by Yafaeva (1959) from Ukraine, Russia. Kasparyan (1974),
however, does not list that reference, nor that host. He records this species
as a usual parasite of Cydia (Cydia) pomonella, distributed in Iran, Central
and Southern Europe, Soviet Central Asia, and Caucasus, etc. Aubert (1969)
lists several common hosts belonging to various families of Lepidoptera and
also Coleoptera: Tenebrionidae. No reared specimen has been seen. The
following description is based upon specimens seen in the Townes Collection.
Male and female: Male flagellum without tyloids. Face a little convex,
shiny, with scattered but distinctly formed punctures. Frons shallowly exca-
vated, minutely punctate, shiny and trans-striate centrally. Ocellar diameter
about equal to ocellocular distance. Interocellar distance 1.2 the ocellocular
V. Gupta: Gypsy Moth Parasites 33
distance. Mesoscutum shiny, with minute scattered and shallow punctures.
Mesopleurum shiny, with minute scattered punctures. Metapleurum shallowly
punctate anteriorly and striato-rugose posteriorly. Propodeum punctato-
rugose, its median carinae distinct in basal 0.3, its basal area smooth.
Coxae not punctate, mat. Fourth tarsal segment of fore leg not deeply notched.
Nervulus interstitial or a little distad of basal vein. First tergite flat in api-
cal half, without humps. Abdominal tergites punctate, punctures well formed
and interspaces shiny. Postpetiole punctate. Apical two tergites smoother.
Apices of all tergites smooth and shiny. All epipleura wide.
Black. Body pubescence white or a little yellowish. Tegula black.
Middle and hind coxae reddish or orange-brown. Fore coxa and trochanters
blackish-brown. Fore and middle legs otherwise and hind trochanters and
femur orange-brown. Hind femur without any fuscous mark. Hind tibia
brownish, without a pale band or with an indistinct pale band, the margins of
which are indistinct. Hind tibial color variable, sometimes entirely red or
reddish-brown. Hind tarsus blackish.
In male the coloration is somewhat different. All coxae are black, first
trochanters blackish, hind tibia black with a pale sub-basal band, and hind
tarsus black. Tegula brownish-yellow. Apical margins of abdominal tergites
subpolished.
Length: Male, 5-8 mm, female, 8-10 mm. Fore wing 4 to 7 mm.
Specimens: Several males and females from Ireland, Scotland, Germany,
Russia and Rumania in the Townes Collection. 19°, Debreczen, Hungary,
1923, R. T. Webber, Gypsy Moth Lab., but without any host label (Hamden).
This species is very close to C. contemplator (Mueller) in sculpture and
general coloration. Both belong to the Aequalis species Group of Townes and
Townes. The latter species, however, can be differentiated by having the
fourth tarsal segment of fore leg apically deeply notched, first two flagellar
segments shorter, less than or just equal to the longitudinal diameter of eye,
and ovipositor sheath equal to or a little shorter than the hind tibia. The male
of C, spurius has the basal half of 6th tergite coarsely punctate, while in the
male of contemplator the 6th tergite is almost impunctate, mat.
Coccygomimus spurius also is close to C. melanacrias (Perkins), the
latter having a distinct white annulus on hind tibia, and apex of hind tibia
fuscous. C. nipponicus (Uchida) and C. confinis (Kasparyan) from Eastern
Palaearctic are also related to spurius and contemplator, but they have black
coxae.
2. Genus ITOPLECTIS (Fig. 2, 126, 127)
Itoptectis Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 164.
For synonymy and relationships with other Ephialtini, refer to Townes
(1969).
Small to medium sized ichneumonids with fore wing 2.5 to 12.5 mm. long.
Clypeus without a transverse suture. Mandible not narrowed apically, teeth
equal to subequal. Occipital and prepectal carinae present. Inner margin of
eye rather strongly concave at antennal socket. Mesopleural suture without a
distinct angulation in the middle. Front tarsal claws of female with a basal
tooth, the middle and hind tarsal claws of female and all tarsal claws of male
simple. Nervellus intercepted far above the middle. Ovipositor straight.
Face and orbits of both sexes entirely black (cf. Ephialtes). Hind tibia
banded (except in viduata) with apical and basal dark bands and a median pale
34 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
band.
Members of the genus Itoplectis are widely distributed. They usually
are internal parasites of lepidopterous pupae, but some (e.g. I. conquisitor
and others) are often secondary parasites of Ichneumonidae, while others may
be normally secondary parasites.
Unlike Coccygomimus and Ephialtes, most species of Itoplectis do not give
off a strong odor when captured or disturbed. :
Five taxa of Itoplectis have been reported as parasitic on the gypsy moth,
viz., I. alternans alternans (Gravenhorst), alternans spectabilis (Matsumura),
conquisitor (Say), maculator maculator (Fabricius), and viduata (Gravenhorst).
Another species, I. clavicornis is here recorded from the gypsy moth. Some
of them, including J, clavicornis, are also hyperparasites of Ichneumonidae
associated with the gypsy moth.
Itoplectis alternans spectabilis (Matsumura) (= Exeristesoides spectabilis)
was first reported from Lymantria dispar in Japan by Fukaya (1936). It is also
a hyperparasite of Hyposoter takagii, and some other ichneumonids and
braconids (Townes etal. 1965). JI. alternans alternans (Gravenhorst) is a
European parasite of Lymantria monacha, which Oehlke (1967) reported from
L. dispar rather than from L. monacha,
Itoplectis conquisitor (Say) (= Pimpla conquisitor) was observed by Howard
and Fiske (1911) to frequently attack gypsy moth pupae in the U.S.A., but the
development of the parasite was rather infrequent. ''Pimpla tenuicornis
Cresson", recorded as a parasite of gypsy moth pupae, by Forbush and
Fernald, but never reared at the laboratory, was believed by Howard and Fiske
to be Itoplectis conquisitor.
Itoplectis maculator maculator (Fabricius) was reported as a parasite of
Lymantria dispar by Oehlke (1967) from Europe. However, I could not trace
it back to its original record and did not see it mentioned in other publications.
Itoplectis viduata (Gravenhorst) (= Pimpla viduata) was reported as a para-
site of Lymantria dispar by Meyer (1929).
Useful taxonomic and biological information on Itoplectis can be found in
Townes and Townes (1960), Sedivy (1963), Townes, Momoi and Townes (1965),
Oehlke (1967), Aubert (1969), Kasparyan (1973) and Carlson (1979).
KEY TO THE SPECIES OF ITOPLECTIS ASSOCIATED WITH
THE GYPSY MOTH
1. Hind tibia uniformly reddish-brown (sometimes with a faint suggestion of a
yellow subbasal band, not sharply demarcated). Coxae and basal tro-
chanteral segments black. Tarsal segments generally pale brownish, not
clearly black marked. Europe, North America, USSR, and China.
5. viduata (Gravenhorst)
Hind tibia with a white or yellow subbasal band. Coxae reddish brown to
2. Antennal flagellum thickened apically, the subapical segments transverse.
Ovipositor sheath short, about as long as the first tergite. Fore and
middle legs largely yellow in male and yellowish-brown in female.
BUraeia, Ry ee ae ea 4. clavicornis (Thomson)
Antennal flagellum not thickened apically, sometimes only slightly wider,
but segments elongate rather than transverse. Ovipositor sheath con-
siderably toneer Man tere bi a a Pr ee re 3
V. Gupta: Gypsy Moth Parasites 39
3. Mesopleurum with dense punctures. In male punctures smaller. All
coxae and basal trochanteral segments black in male and female.
Abdominal tergites usually reddish-brown laterally, sometimes apically
9160. PURO SA uici a eee he ek Fe oe Re ie 3. maculator (Fabricius)
Mesopleurum finely punctate. Coxae and trochanters reddish-brown except
in male of alternans where hind coxa black. Abdominal tergites narrowly
yellow apically, or not so. Sides of tergites not reddish or yellow. . 4
4. Ovipositor sheath long, about 2.0-2.2 times the length of first tergite and
1.5 times the length of hind femur. Hind femur with a fuscous black
apical mark. Punctures on abdominal tergites uniform, regular but on
tergites 4-5 of male rather sparse. Pale bands on tergites rather con-
epieuous.... North Americans & 4 ff cnie ward 1. conquisitor (Say)
Ovipositor sheaths shorter, about 1.5-1.7 as long as the first tergite
and 1.1-1.2 as long as the hind femur. Hind femur without a fuscous
apical mark. Pale bands on tergites faint to inconspicuous. Tergites
coarsely DUNClate sci oc ase) Gide eas os pees UR 2. alternans. . 5
5. Trochanters reddish-brown in female and yellow inmale. Fore and
middle legs reddish-brown in female and yellow inmale. Basal black
mark on hind tibia wider so that the yellow band is narrow. Apical half
of hind tibia often reddish-brown rather than black. Eurasia.
2a. alternans alternans (Gravenhorst)
Trochanters reddish with yellow markings. Fore and middle legs largely
yellow or yellowish-brown. Basal black mark on hind tibia very small,
so that the yellow band is wide. Apical half of hind tibia black. Japan
end Far Chet. <nceks oes a 2b. alternans spectabilis (Matsumura)
1. ITOPLECTIS CONQUISITOR (Say) (Figs. 38,40, 42, 127)
Cryptus conquisitor Say, 1936. Boston J. Nat. Hist., 1: 232.
Pimpla conquisitor: Howard and Fiske, 1911. U.S. Dept. Agr. Bur.
Ent. Bull., 91: 138, 237.
Itoplectis conquisitor: Townes and Townes, 1960, U. S. Natl. Mus. Bull.,
216(2): 287.
Itoplectis conquisitory: Campbell, 1963. Canad. Ent., 95: 337.
Itoplectis conquisitor: Carlson, 1979. In Krombein, etal. Catalog of
Hymenoptera in America north of Mexico, 1: 340.
Useful taxonomical and biological references are given in Townes and
Townes (1960) and Carlson (1979). Information pertaining to the association of
this parasite with the gypsy moth is given by Howard and Fiske (1911) and
Campbell (1963).
Male and female: Flagellum weakly widened apically. Temple receding
from eye. Face moderately wide, punctate. Mesoscutum and mesopleurum
with scattered small punctures. Notauli absent. Propodeum short, its medium
carinae extending up to 0.3 its length. Fore tarsal claw of female with a large,
broad tooth. Third tergite about as long as wide in male and 0.5 to 0.6 as long
as wide infemale. Fourth and fifth tergites of male polished and with widely
separated punctures. In females punctures dense. Tergites 2-7 with weak
depressions and elevations. Ovipositor sheath about 2.2 as long as the first
tergite.
36 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Black. Palpi of male white. Maxillary palpus of female white. Labial
palpus of female light brown. Scape and pedicel of male antenna white in
front. Flagellum reddish-brown beneath, more extensively so inmale. Tegula
and hind corner of pronotum white. Legs of female largely reddish-brown.
Fore coxa blackish basally. Fore tibia and tarsus with faint yellow patches.
Middle tibia with a pale subbasal band. Middle tarsal segment yellowish
basally and fuscous apically. Apex of hind femur, base and apical 0.4 of hind
tibia and apical half of hind tarsal segments black. Fourth tarsal segment
wholly black. Hind tibia with a broad yellowish-white subbasal band. Hind
tarsal segments whitish in basal half. In male, fore and middle legs largely
yellow with tibiae yellowish-brown. Hind leg color same as in the female.
Apices of abdominal tergites yellow.
Length: 9-14mm. Fore wing 6.0-2.5 mm. Some specimens are rather
short, 5-6 mm. long.
Specimens: Several males and females from different states of U.S.A.,
in Townes Collections. No reared specimens from the gypsy moth seen.
This species is readily distinguished by the color pattern of its legs and
abdomen. The hind leg and abdomen gives a banded appearance. The sculpture
of the fourth and fifth tergites of male is characteristic.
Itoplectis conquisitor is a polyphagous parasite and is hyperparasitic upon
occasions. It is widely distributed in the Nearctic Region. Howard and Fiske
(1911) observed that this parasite frequently attacked the gypsy moth pupae, but
that the young larvae of it rarely completed their development upon it.
Campbell (1963) substantiated those findings. He observed that Itoplectis con-
quisitory stung a number of prepupae and pupae of gypsy moth in the field, but
hardly ever developed upon them. The species preferred to hunt in the open
and exhibited a striking positive response to defoliated areas. In the Glenville
area, it was the dominant species attacking gypsy moth pupae and prepupae.
Adults occurred from early spring to late fall. A wide variety of exposed or
weakly protected lepidopterous pupae or prepupae served as hosts. Develop-
ment from egg to adult took about 20 days.
Itoplectis conquisitor apparently attacks the gypsy moth pupae and pre-
pupae for getting food, rather than oviposition. However, in this process they
puncture the pupal skin and kill the host. Sarcophagids oviposit in such pupae.
They have a scavenger relationship with the host.
This species therefore kills pupae of the gypsy moth in large numbers.
Three other native Ichneumonids, Coccygomimus pedalis, Theronia atalantae
and Theronia hilaris have also been observed to kill more pupae than they
parasitize, thus exerting a greater influence on the populations of gypsy moth
than is usually credited to the Ichneumonidae. |
Further information on its biology and biological references are given by
Townes (1940) and Townes and Townes (1960).
2a. ITOPLECTIS ALTERNANS ALTERNANS (Gravenhorst) (Figs. 12, 30, 36,
37, 39, 126)
Pimpla alternans Gravenhorst, 1829. Ichneumonologia Europaea, 3: 201.
Europe.
Itoplectis alternans: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 38. Hosts and distributional records in Eastern
Palaearctic Region.
Itoplectis alternans:Oehlke, 1967. Hymenopterorum Catalogus (nova
editio), 2(1): 26. Palaearctic. Various hosts including Lymantria
dispar
V. Gupta: Gypsy Moth Parasites 37
Oehlke (1967) provides some biological references. Kasparyan (1973)
provides a key to the Eurasian species of Itoplectis.
This subspecies is extremely close to Itoplectis conquisitor from North
America, differing mainly as follows:
Mesopleural punctures sparser and minute. Propodeal carinae short and
widely diverging. Propodeum smoother. Abdominal punctures coarse and con-
tiguous in both the sexes. Ovipositor short, its sheaths 1.5 to 1.7 as long as
the first tergite and about 1.1 to 1.2 as long as the hind femur.
Hind corner of pronotum very narrowly yellow, mainly in the region of
postspiracular sclerite. Palpi yellowish-brown. Fore coxa usually reddish-
brown. Hind femur without an apical fuscous mark. Apex of hind tibia
reddish-brown. Abdominal tergites with faint to rather narrow brownish mar-
gins.
Length: 5-7 mm. Fore wing 4-6 mm.
Specimens: Italy: Portici, 1%, 49, 1912, ex Hyposoter disparis Vier.
[= Phobocampe unicincta], Gypsy Moth Lab., No. 7429F and 7429 (Hamden).
Hungary: Olasziszka, 1%, June 25, 1927, ex Lymantria dispar, labelled
Ephialtes (Itoplectis) sp. (Hamden). Several unreared %, ¥ from Europe
(Townes Coll.).
The above specimens reared at the Gypsy Moth Laboratory, indicate that it
is a primary parasite of the gypsy moth, as well as a hyperparasite of a
gypsy moth parasite, Phobocampe unicincta, In literature (Townes ef al.,
1965, Aubert, 1969, etc.) it is reported as a parasite of several other Lepidop-
tera including L. monacha, and as a hyperparasite of Rhogas, Casinaria and
Hyposoter species.
2b. ITOPLECTIS ALTERNANS SPECTABILIS (Matsumura)
Pimpla (Pimpla) spectabilis Matsumura, 1926. J. Coll. Agr. Hokkaido
Imp. Univ., 18: 30. Japan. Host: Dendrolimus spectabilis.
Exeristesoides spectabilis: Fukaya, 1936. Oyo Dobutsugaku Zasshi,
8: 232, 335. Japan. Host: Lymantria dispar.
Itoplectis alternans spectabilis: Townes, Momoi and Townes, 1965. Mem.
Amer. Ent. Inst., 5: 38. China, Japan, Korea. Several hosts in
Japan.
This subspecies is close to Itoplectis conquisitor and differs from the latter
as given in the key and under J. alternans alternans. It differs from the sub-
species alteynans in having a rather broad yellowish-white band on hind tibia,
with the basal black mark small to almost obliterated and apical black mark
prominent. The fore and middle legs are lighter incolor. In males they are
largely yellow.
Length: 5-7 mm. Fore wing 4-5 mm.
Specimens examined: Japan: 2%, 42, reared from Gvapholitha molesta
(Townes Coll.). No specimens reared from gypsy moth seen. It has been
reported as a hyperparasite of Hyposoter takagii, Eriborus molestae, and
Apanteles sp. in Japan.
3. ITOPLECTIS MACULATOR MACULATOR (Fabricius) (Fig. 2)
Ichneumon maculator Fabricius, 1775. Systema Entomologiae, p. 337.
Germany.
Itoplectis maculator: Townes, Momoi and Townes, 1965. Mem. Amer.
38 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Ent. Inst., 5: 40. Eurasia, North America, North Africa.
Synonymical references and host records.
Itoplectis maculator maculator: Oehlke, 1967. Hymenopterorum
Catalogus (nova editio), 2 (1): 28. Host: Lymantria dispar, besides
several other hosts. |
This species conforms in general to the description of I. conquisitor and is
differentiated as follows:
Thorax rather closely punctate. Mesoscutum with small close punctures.
Mesopleurum with dense well formed punctures, which are of moderate size
and depth. In males punctures smaller. Propodeum densely punctate laterally,
smoother medially, its median carinae extending in basal 0.25 and weakly
diverging apically. Punctures on abdominal tergites dense and coalescing.
Coxae and first trochanteral segments of all legs black. Fore and middle
legs yellowish-brown, with yellow patches. Hind leg brownish-yellow or
orange colored, with tibia having a yellow sub-basal band and tarsal segments
basally yellow. Abdominal tergites laterally brownish. Their apices also
brownish. Extent of lateral brownish marks on tergites variable, sometimes
tergites more extensively brownish-yellow, particularly in males.
Length: 5-10 mm. Fore wing 4 to 7.5 mm.
Specimens: Spain: Madrid, 1°, June 1925, Lymantria dispar, Gypsy
Moth Lab. Italy: Portici, 1%, 1912, ex Hyposoter disparis Vier. [= Phobo-
campe unicincta], Gypsy Moth Lab., No. 7429e. 19, "bred from P, dispar", ~
Gypsy Moth Lab., No. 1094, July 15, labelled "Scambus maculatus F. (All ~
Hamden).
Distribution: Eurasia, N. Africa, and N. America. Walkley (1958)
recorded its establishment in North America in Oregon. See Townes and
Townes (1960) and Carlson (1979) for further information about its establish-
ment in the U.S.A., and for biological references.
Sedivy (1963) provided a list of hosts in Europe and Meyer (1934) in USSR.
The above mentioned specimens indicate its occurrence at times as para-
sitic on Lymantria dispar, and that it is hyperparasitic on occasion. Vasic
(1958) reported that it parasitized 25% of Casinaria tenuiventris cocoons in
Yugoslavia.
4. ITOPLECTIS CLAVICORNIS (Thomson)
Pimpla clavicornis Thomson, 1889. Opusc. Ent., 13: 1409. Europe.
Itoplectis clavicornis: Oehlke, 1967. Hymenopterorum Catalogus (nova
editio), 2(1): 27. Europe. England.
According to Townes and Townes (1960) J. clavicornis is usually a
secondary parasite on Ichneumonidae. It is a rather distinct species with
flagellum thickened apically, the subapical segments being wider than long.
Ovipositor short. Ovipositor sheaths about as long as the first tergite. Meso-
pleurum smoother, polished. Median propodeal carinae short. Abdomen
slender, punctate.
Legs in general yellowish-brown with hind femur orange colored and with-
out any apical fuscous mark. Hind tibia with a broad yellow sub-basal band.
Fore and middle legs in male more yellow. Hind coxa of male black and that
of female brown to partly blackish. Abdominal tergites without conspicuous
pale bands.
Length: 8-9mm. Fore wing 5-6 mm.
V. Gupta: Gypsy Moth Parasites 39
Specimens: Italy; Portici, 1912, 1°, 12, ex Hyposoter disparis Vier.
[=Phobocampe unicincta], Gypsy Moth Lab., No. 5427 and 7435 DA. Hungary:
Vees, 3%, May 138, 1929, ex Hyposoter disparis, Gypsy Moth Lab., No. 13039
D (Hamden).
Distribution: Europe.
The above specimens attest to the fact that J. clavicornis is a hyperpara-
site of Phobocampe unicincta and not useful in the control of the gypsy moth.
9. ITOPLECTIS VIDUATA (Gravenhorst)
Pimpla viduata Gravenhorst, 1829. Ichneumonologia Europaea, 3: 214.
Europe.
Pimpla viduata: Meyer, 1929. Izv. Otd. Prikl. Ent. GIOA (Repts. Bur.
Appl. Ent.), 4: 235, 240. USSR. Hosts: Lymantria dispar and
Cosmia subtilis.
Itoplectis viduata: Townes and Townes, 1960. U. S. Natl. Mus. Bull.,
216(2): 293. China: Manchuria, Europe, N. America. Various
hosts in North America.
This species is readily distinguished from all other species of Itoplectis by
its hind tibia being uniformly reddish-brown and all coxae and first trochanteral
segments black. Middle and hind coxae are not mentioned to be black in
European specimens by Kasparyan (1973).
It is somewhat robust species with deeper punctation on mesoscutum and
mesopleurum, propodeal spiracles elongate-oval (usually short oval), pro-
podeum punctate laterally, its median carinae extending up to the middle,
abdominal tergites strongly punctate, and ovipositor sheath about 2.5 as long
as the first tergite.
All legs uniformly orange to reddish-brown, with their coxae and tro-
chanters black (Nearctic specimens seen). Abdomen without yellow bands.
Length: 9-12 mm. Fore wing 7.5 to 11.5 mm.
Specimens: 3%, 32, from California, Colorado and Arizona in Townes
Collection. No reared specimens seen.
Distribution: Widely distributed in Europe, USSR and western North
America.
Hosts: Recorded as a parasite of Lymantria dispar by Meyer (1929).
Townes and Townes (1960) list several hosts in North America. Aubert (1969)
lists European hosts.
3. Genus EPHIALTES (Figs. 3, 128, 129)
Ephialtes Schrank, 1802. Fauna Boica, 2: 316.
This genus has often been called Apechthis. Refer to Townes (1969) for
synonymy and its relationships with other members of the tribe Ephialtini,
subfamily Pimplinae. :
Ephialtes can easily be distinguished from other pimpline ichneumonids by
its sharply decurved ovipositor tip. It is further characterized by having the
face of the male largely to entirely white or yellow. Orbit of female narrowly
whitish in front. Inner margin of eye rather strongly concave opposite antennal
sockets. Malar space 0.15 to 0.2 the basal width of mandible. Clypeus nor-
mally formed, basally a little concave, without any transverse suture. Man-
dible broad, teeth subequal. Notauli weak or absent. Propodeum with only
40 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
median carinae extending in basal 0.5 to 0.7. Fore, middle and sometimes
the hind tarsal claws of female with a large tooth. Tarsal claws without an
enlarged flat-tipped hair. Nervellus intercepted well above the middle.
Abdomen with coarse punctures. Epipleurum of fifth tergite narrow, at least
3.0 as long as wide in female and 4.0 in male.
Members of the genus Ephialtes are medium-sized to moderately large
ichneumon-flies. They are internal parasites of lepidopterous prepupae or
pupae.
Three species have been reported in literature as being parasitic upon
Lymantria dispar. These are Ephialtes compunctor (L.) (= brassicariae),
E, rufatus (Gmelin) (= vufata Gravenhorst), and E. capulifera (Kriechbaumer).
They have not been commonly encountered, however.
Howard and Fiske (1911) reported rearing Ephialtes compunctor (L.) (as
Pimpla brassicariae Poda) at the Gypsy Moth Laboratory (Massachusetts)
infrequently from the European collections of the gypsy moth and the brown tail
moth. Rudow (1911) mentioned Pimpla varicornis Gr. = compunctor (L.)
as a parasite of gypsy moth and the nun moth. Stadler (1933) mentioned it
(=P. brassicariae) as a parasite of Lymantria dispar in Europe.
Rudow (1911) reported Ephialtes rufatus (Gmelin) (= Pimpla rufata Grav.)
as a parasite of Lymantria dispar and L. monacha in Europe. Meyer (1927)
reported it from the gypsy moth in Russia. However, he did not mention this
host in his subsequent publications on USSR Ichneumonidae (Meyer, 1934,
1936). Thompson's source was Meyer (1927) (RAE, A, 16: 200).
Ephialtes capulifera (Kriechbaumer) was first reported as a parasite of
Lymantria dispar by Uchida (1958) (as Apechthis capulifera var. nigriabdom-
inalis) in Japan. Kamijo (1962) gave some biological notes.
All these three species have been frequently mentioned as parasites of
Lymantria monacha as well as several other hosts in Europe and Japan.
Aubert (1969) and Townes e/ al. (1965) may be consulted for listings of hosts,
taxonomic references and distributional records.
"Pimpla dentator Thomson" mentioned in literature as a parasite of
Lymantria monacha is a lapsus for Pimpla quadridentata Thomson, which is a
species of Ephialtes.
KEY TO THE SPECIES OF EPHIALTES PARASITIC
UPON THE GYPSY MOTH
1. Hind coxa and apex of hind femur black. Usually all coxae black and hind
femur black. Tibia black, with a wide pale submedian band. Body
pubescence white. Eurasia and Far East.
1. capulifera (Kriechbaumer)
Hind coxa and hind Temur usually wholly reddish. . osc 2 kes eR 2
2. Body pubescence brownish. Mesoscutum without yellow markings, except
sometimes inmales. Scutellum narrowly yellow apically. Metascutellum
black. First tergite with two conical projections in the middle. Hind
tibia without any pale band, rust-red colored (except faintly so in a sub-
Species, orientalis, from Eastern Siberia). ... 2. compunctor (L.)
Body pubescence whitish. Mesoscutum with two stripes beyond its middle
and usually also along its basolateral corners. Scutellum largely
yellow. Metascutellum yellow. First tergite without conical projections,
only convexly angled medially. Hind tibia with a faint to somewhat distinct
V. Gupta: Gypsy Moth Parasites 41
Wile DANA Os re eer are es 3. rufatus (Gmelin)
1. EPHIALTES CAPULIFERA (Kriechbaumer)
Pimpla destructor Smith, 1874. Trans. Ent. Soc. London, 1874: 394.
Japan. Name preoccupied by Smith, 1863.
Pimpla capulifeva Kriechbaumer, 1887. Ent. Nachr., 13: 119. Germany.
Apechthis capulifera var. nigriorbitalis Uchida, 1958. Shin Konchu,
8(5): 8. Japan. Hosts: Lymantria dispar and others.
Apechthis capulifera: Kamijo, 1962. Koshunai Rinboku Ikushujo Hokoku,
1: 87. biol. Japan. Host: Lymantria dispar.
Male and female: Face a little longer than wide, with scattered punctures,
wrinkled in a median area below antennal sockets. Clypeus basally a little con-
vex and with scattered punctures, its apical 0.75 flat and somewhat mat.
Malar space 0.2 the basal width of mandible. Frons and vertex smooth. Inter-
ocellar distance 1.7 to 1.8 the ocellocular distance. Vertex narrow, sharply
receding from behind ocelli. Mesoscutum dull mat, leathery in texture. Scu-
tellum subpolished with scattered minute punctures. Pronotum polished, with
scattered minute punctures along its upper margin. Mesopleurum polished
and with scattered punctures, speculum glabrous. Metapleurum polished with
minute punctures in its upper 0.3. In larger specimens the punctures a little
spread out on side of thorax. Propodeal spiracle oval, small. Propodeum
finely rugoso-punctate except the petiolar area which is smooth. Median pro-
podeal carinae a little diverging apically and ending in the middle of propodeum.
Area between the carinae smooth. Areolet more trapezoidal with first inter-
cubitus shorter than the second and second recurrent in the apical 0.3. Abdo-
men closely punctate. First tergite with coarser shallow punctures, tending
to be shallowly rugoso-punctate. Its median dorsal carinae forming moder-
ately convex humps, broadly angulate in the female and evenly rounded in the
male. Ovipositor sharply decurved, though not quite angled or L-shaped, more
sigmoid.
Black. Flagellum black or yellowish-brown ventrally and darker dorsally.
Face narrowly yellow along inner orbits and sometimes on vertical orbits.
Palpi and tegula brown. Scutellum and metascutellum apically yellow. Coxae
wholly to largely black. Legs otherwise yellowish-brown with yellow patches
on fore femur, tibia and tarsus, middle tibia and tarsus, and apex of middle
femur. Hind tibia with a broad yellow sub-basal band. Apex of hind femur,
tibia except for the yellow band, and hind tarsus black to blackish-brown.
Stigma and veins brownish-black. Body pubescence white.
In many specimens from Japan (var. sapporoensis) the legs are more
extensively black, with hind femur wholly black and black marks on trochanters
and middle femur. The tegula is also blackish. In some other specimens the
coxae are partly black and partly yellow, and yellow on hind tibia more exten-
sive. The face is more extensively yellow on sides. The scutellum and meta-
scutellum are also yellow. A few specimens, usually the males have the legs
extensively yellow. A female from Hungary from gypsy moth has all femora
orange colored and all coxae black.
Length: 12-18 mm. Fore wing 10-13 mm.
Specimens: Hungary: Baja, 12, ex Lymantria dispar, "Gipsy Moth Lab.,
No. 3483C''. (labelled as Apechthis sp 1) (Hamden). Japan: Hokkaido,
Higashimokoto, 1°, July 24, 1978, ex pupa of Lymantria dispar, P. Schaefer
42 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
(BIRL, Delaware). Hokkaido, Jyozonkei, 1°, July 21, 1975, emerged from
pupa of Lymantria dispar, August 4, 1975, P. Schaefer (BIRL, Delaware).
Several “? from Japan (Townes Coll.).
Distribution: Eurasia, Japan, Korea, Taiwan and China. According to
Kasparyan (1973) it is a transpalaearctic forest species, which is of rather rare
occurrence in the European part of USSR.
Hosts: Lymantria dispar, L. monacha and several other hosts belonging
to the following families (cf. Aubert, 1969): Tortricidae, Geometridae,
Lasiocampidae, Arctiidae, Lymantriidae, Noctuidae, Hesperidae, Papilioni-
dae, Pierididae, Nymphalidae, and Cerambycidae.
2. EPHIALTES COMPUNCTOR (Linnaeus) (Figs. 3, 128)
Ichneumon compunctor Linnaeus, 1758. Systema Naturae,(Ed. 10) 1: 564.
Europe.
Ichneumon brassicariae Poda, 1761. Insecta Musei Graecensis, p. 105.
Yugoslavia. Host: Pieri brassicariae.
Pimpla (Apechthis) brassicariae: Howard and Fiske, 1911. U. S. Dept.
: Agri. Bur. Ent. Bull., 91: 85, 238. Host: Lymantria dispar.
Ephialies compunctor: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 44. References.
Male and female: Essentially similar in sculpture to E, capulifera and
differing as follows:
Metapleurum largely smooth and polished. First tergite convex and dor-
sally humped, with its median carinae angled in the middle, the area between
them depressed. Fifth tergite shallowly punctate with interspaces shiny. Side
of thorax more polished. Propodeum basally smoother. Median propodeal
carinae longer, extending up to basal 0.4 to 0.5 and widely diverging. Areolet
more triangular, with second recurrent vein near its middle. Ovipositor tip
strongly decurved, almost L-shaped.
Black. Flagellum yellowish-brown. Palpi and tegula blackish-brown.
Scutellum yellow near metascutellum. Metascutellum black or only faintly
yellow-marked. Mesoscutum as a rule without yellow markings, yellow
markings only sometimes present in males. Legs largely reddish-brown with
fore coxa and base of middle coxa sometimes black. Hind tibia rust-red,
usually without banding (except faintly so in compunctor orientalis Kasparyan).
Hind tarsal segments fuscous apically. Body pubescence brownish.
Length: 12-16 mm. Fore wing 10-12 mm.
Specimens: France: Charroux, 12, bred from Lymantria dispar, Gypsy
Moth Lab, No. 1683, det. as Apechthis brassicariae Poda, by Muesebeck.
Germany, 1%, bred from Lymantria dispar, Gypsy Moth Lab, No. 829 Ag 5
(Hamden). Several males and females from Europe in Townes Collection.
Distribution: Europe, Russia, Japan and Korea. Kasparyan (1973)
described an Eastern Siberian subspecies, E. compunctor orientalis, with
banded hind tibia.
Hosts: A polyphagous parasite developing within the pupae of several
families of Lepidoptera and some Coleoptera (cf. Aubert, 1969), including
Lymantria dispar and L. monacha. Townes, etal. (1965) give host records
from Japan and Russia. Hedlund and Mihalache (1980) reared two specimens
of Ephialtes compunctor from the gypsy moth from Site B in Southern Rumania,
which they considered to be a new host record. According to them the para-
sitism was less than 1%. Vasic (1958) reported it from Yugoslavia from the
gypsy moth.
V. Gupta: Gypsy Moth Parasites 43
3. EPHIALTES RUFATUS (Gmelin) (Fig. 129)
Ichneumon rufatus Gmelin, 1790. Im Linnaeus: Systema Naturae, Ed
13 (1) 5: 2684. Europe. |
Pimpla rufata: Gravenhorst, 1829. Ichneumonologia Europaea, 3: 164.
Europe.
Pimpla rufata;Grav.: Rudow, 1911. Internatl. Ent. Ztschr., 9: 99.
Europe. Hosts: Lymantria monacha, L. dispar.
Pimpla rufata: Meyer, 1927, Izv. Otd. Prikl. Ent. GIOA (Repts. Bur.
Appl. Ent.), 3 (1): 75-91. Russia. Hosts: Lymantria dispar,
Aporia crataegi, Malacosoma neustria, Diprion pini.
Ephialtes rufatus: Townes, Momoi and Townes, 1965. Mem. Amer. Ent.
Inst., 5:45. Germany, Japan, Kamchatka, Korea, Kuriles, Russia,
Sakhalin. Full synonymical references and hosts.
Further taxonomical and biological references are given by Oehlke (1967)
and Aubert (1969), which may also be consulted for the various hosts.
Essentially similar in sculpture to Ephialtes capulifera, and differing as
follows:
Malar space 0.25 the basal width of mandible. Metapleurum with
scattered punctures. Propodeum smoother basally. Propodeal sculpture
less coarse and somewhat shiny. Median propodeal carinae generally shorter,
almost parallel-sided and ending in a central rugose area. Propodeal
spiracles bean-shaped. Areolet more triangular in outline, with the two inter-
cubiti almost equal and second recurrent vein meeting areolet close to its
middle. First tergite not conspicuously humped medially. Abdominal tergites
less closely punctate. Punctures on fourth and fifth tergites well separated
with interspaces shiny. Ovipositor tip only slightly decurved.
Black. Face, frons and vertex with narrow yellow orbital lines. Flagellum
yellowish-brown ventrally and blackish dorsally. Palpi and tegula orange-
yellow. Mesoscutum with two yellow lines behind its middle. Sometimes
its antero-lateral corners also yellow. Scutellum broadly and metascutellum
almost wholly yellow. Legs, including coxae, reddish-brown, with yellow
patches on fore trochanters, apex of femur, tibia and tarsus. Apex of middle
femur, tibia and tarsus also with yellow marks. Hind tibia fuscous at extreme
base and with a faint to rather distinct sub-basal yellow band. Hind basitarsus
yellow except apically. Coxae partly black in Japanese populations (rufatus
geometriae). Body pubescence whitish.
Length: 10-15 mm. Fore wing 8-12 mm.
Specimens: Several males and females, from Europe and Japan in Townes
Collection. No reared specimens seen. The Japanese populations have the
coxae black marked and yellow band on hind tibia more pronounced. Perhaps
they do represent a distinct subspecies, Ephialtes rufatus geometriae Uchida,
1928. This has, however, been synonymized under the nominate subspecies
(Townes et al. , 1965).
Distribution: Europe, Russia, Japan and Korea.
Hosts: Lymantria dispar, L. monacha, and several others belonging to
various families of Lepidoptera (Townes, Momoi and Townes, 1965). Aubert
(1969) records the hosts from Europe, including a few cases of parasitism of
Diprionidae. Vasic (1958) reported it from the gypsy moth in Yugoslavia.
4G, Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Tribe THE RONIINI
Members of the tribe Theroniini are characterized by having the meso-
pleural suture angulate near middle, propodeum more or less areolated,
areola often distinctly formed, tarsal claws simple, without a basal lobe,
areolet present, subgenital plate of male often longer than wide, and ovi-
positor short to long, of uniform width.
Only one genus Theronia is associated with the gypsy moth. They are
usually yellowish-brown in color (although some species are black) and have
an enlarged hair on each tarsal claw which is flattened at the tip.
4. Genus THERONIA (Figs. 4, 182)
Theronia Holmgren, 1859. Ofvers. Svenska Vetensk. Akad. Forh.,
16: 123.
Townes (1969) may be consulted for generic synonymy and key to distin-
suish it from other Theroniini.
Mandible not strongly tapered, its teeth equal. Clypeus truncate or witha
median notch. Prepectal carina present. Mesopleural suture with a weak
angulation near middle. Propodeal carinae strong. Tarsal claws very large,
simple, but with an enlarged bristle arising sub-basally below and extending
to apex of claw, the tip of the bristle with a spatulate enlargement. Nervellus
intercepted far above the middle. Areolet present. Abdomen polished, with
minute setiferous punctures. Ovipositor short to moderately long, cylindric,
its sheath usually about 0.45 as long as the forewing.
Species of Theronia are medium-sized ichneumonids inhabiting mostly
dense forests. They are pale colored and generally fly low. They are primary
or secondary parasites within lepidopterous pupae. Some species parasitize
pupae of aculeate wasps in their nests. The egg is deposited within the pre-
pupa or a freshly formed pupa and emergence is from the pupa. As a primary
parasite the insect lives within its host. If the host attacked has already been
attacked by another ichneumonid, it becomes a secondary parasite external to
the latter. The larvae of Theronia have a large internal tooth on the mandible.
Two species, Theronia atalantae (and its subspecies) and T. hilaris
(= melanocephala) have been associated with gypsy moth. T. atalantae has been
commonly reared from the gypsy moth in Europe, USSR, North America, and
Japan. A subspecies of it occurs on Lymantria obfuscata in India. T. zebra
diluta was reported from Lymantria serva in Taiwan by Gupta (1962).
T. atalantae and T. hilaris have been reported as hyperparasitic on other
ichneumonids associated with the gypsy moth on occasions.
KEY TO THE SPECIES AND SUBSPECIES OF THERONIA
ASSOCIATED WITH THE GYPSY MOTH |
1. Hind femur sharp beneath for part of its length, and usually with a weak to
sharply irregularly serrate ridge. Head rufous-brown.
Dots MAEM ey oes RR Ra 2
Hind femur rounded beneath, without a ridge. Head black. (In other
subspecies from Europe and Japan whole body black). North America.
2. hilaris hilaris (Say)
V. Gupta: Gypsy Moth Parasites 45
2. Abdominal tergites with dark brown to black basal bands or spots. Flagel-
lum brown. Thorax with extensive fuscous markings. Japan, Korea,
Manchuria, and Siberia. .... . 2c. atalantae gestator (Thunberg)
Abdominal tergites uniformly rufous brown, or rarely with a few spots.
Thorax rufous brown or a few spots and stripes on mesopleurum, base
of propodeum oF around etutelluny ic sos ha enh Re WR. Sle 3
3. Wings dark brown. Flagellum blackish-brown to black. Ridge or crest
along lower margin of hind femur weak. Mesopleurum and base of
scutellum with fuscous markings. India: Kashmir and Himachal
Pradesh: a5 OE eee 1d. atalantae himalayensis, n. subsp.
Wings clear hyaline, or only lightly yellowish-tinged. Flagellum black to
brown. Lower margin or hind femur usually with a serrated ridge.
Fuscous marks on thorax absent or less extensive (except sometimes in
in tetinnteae bel i. SES GRE OPO A GS: a 4
4. Flagellum light brown, of the same color as the thorax. Mesopleurum
often with fuscous markings. Sometimes mesoscutum also with fuscous
markings; “Barenep ice. Wad Ges la. atalantae atalantae (Poda)
Flagellum dark brown, darker in color than the thorax. Mesopleurum
partly to largely yellowish, usually without fuscous markings. North
AOROTICA CA CAN ORME 1b. atalantae fulvescens (Cresson)
1. THERONIA ATALANTAE (Poda) (Figs. 4, 132)
Clypeus apically thin and only slightly concave. Prepectal carina roundly
curved forward and almost reaching margin of pronotum. Notauli distinct at
front end of mesoscutum. Scutellum not carinate laterally. Thorax shiny,
with minute scattered setiferous punctures. Propodeal spiracle elongate,
linear. Median and lateral propodeal carinae present. Median carinae
parallel-sided and extending to middle of propodeum, where they meet the
strongly curved apical transverse carina. Lateral carinae obsolete basally,
opposite spiracles. Petiolar area hexagonal. Median section of apical trans-
verse carina bounding the combined areola and basal area often dipped and
notched in the middle in the female. Hind femur with a ventral crest or ridge,
which is often serrate in larger specimens. First tergite about 1.5 as long
as wide and with strong dorsal carinae. Abdomen polished. Ovipositor about
0.7-0.75 as long as the abdomen, its sheaths about 1.5 as long as the hind
femur.
Rufous-brown. Wings hyaline or brown tinged. Thorax and abdomen with
or without fuscous marks depending upon the subspecies.
Size variable, depending upon the host. Those reared from ichneumonid
hosts much smaller than those reared from the gypsy moth.
la. THERONIA ATALANTAE ATALANTAE (Poda) (Figs. 4, 24,41, 132)
Ichneumon atalantae Poda, 1761. Insecta Musei Graecensis, p. 106.
Europe. Host: Vanessa atalantia.
Ichneumon flavicans Fabricius, 1793. Ent. Syst., 2: 182. Germany.
Pimpla flavicans Fabr.: Ratzeburg, 1844: 118. Germany. Hosts: pupae
of Aporia crataegt, Dendrolimus pini, and Lymantria dispar.
46 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Theronia atalantae: Howard and Fiske, 1911. U.S. Dept. Agr. Bur.
Ent. Bull., 91: 85, 236. Lab. reared from gypsy moth.
Theronia atalantae atalantae: Townes and Townes, 1960. U. S. Natl.
Mus. Bull., 216(2): 354.
This subspecies has several synonyms in Europe. Refer to Townes,
Momoi and Townes (1965) and Oehlke (1967) for synonymical references, and
host records.
Ratzeburg (1844) first reported it from Lymantria dispar in Europe.
Howard and Fiske reared it in the Gypsy Moth Laboratory from shipments of
gypsy moth pupae from Europe. Several authors have recorded it as a para-
site of the gypsy moth in Europe (Thompson, 1946). Some of the recent
studies are of Gyorfi (1963), and Hedlund and Mihalache (1980).
Theronia atalantae atalantae is characterized by having the flagellum light
brown in color (resembling the coloration of the thorax), mesopleurum brown-
ish, mesoscutum and mesopleurum usually with only small fuscous marks,
which at times may be extensive, or reduced, wings light yellowish-hyaline,
and legs and abdomen pale yellowish-brown, without fuscous marks. The
scutellum is yellow. Two females in Townes Collection from Germany and
Poland have extensive fuscous marks on thorax, and hind coxae partly black-
ish.
Length: 8-13 mm. Fore wing 7-11 mm.
Specimens: Southern Rumania: Site B, 1°, 1°, July 1978, ex Lymantria
dispar pupae, R. C. Hedlund (E.P.L., Paris). Hungary: Vees, 2%, July 12,
1928, ex Hyposoter sp., Gypsy Moth Lab., Nos. 13039D and 13039B2.
Hungary: Olaszliszka, 2°, bred from L. dispar, Gypsy Moth Lab., No.
13028B. Italy, 1%, July 22, 1911, bred from L. dispar, Gypsy Moth Lab. ,
No. 3416. Italy, 1%, June 1911, ex Hyposoter disparis, Gypsy Moth Lab.,
No. 3410B (all FIS, Hamden). Several males and females without host data,
from Europe in Townes Collection.
Distribution: Widely distributed in Europe.
Hosts: Several hosts are recorded from Europe and USSR, including
Lymantris dispar and L. monacha. It is also recorded as a hyperparasite of
genera like Casinaria, Iseropus, Rhogas, etc. It is here recorded as a
hyperparasite of Phobocampe unicincta (= Hyposoter disparis).
It is likely that many USSR records may pertain to T. atalantae gesiator,
which occurs in the Asian part of USSR.
It is a casual parasite of the pupae of Lymantria dispar and has never
been reared in abundance on that host, although it is likely that it may be
killing more host pupae by puncturing the pupae than by parasitizing, as has
been seen in the U.S.A. by Campbell (1963) in T. atalantae fulvescens.
ib. THERONIA ATALANTAE FULVESCENS (Cresson) (Fig. 18)
Pimpla fulvescens Cresson, 1865. Proc. Ent. Soc. Philadelphia, 4: 268.
U.S.A.: Colorado.
Theronia fulvescens: Howard and Fiske, 1911. U.S. Dept. Agr. Bur.
Ent. Bull., 91: 137, 141, 142, 236-237. Hosts: Lymantria dispar,
Euproctis chrysorrhoea,
Theronia atalaniae fulvescens: Townes and Townes, 1960. U. S. Natl.
Mus. Bull., 216(2): 354. Syn., distribution and biological refer-
ences.
V. Gupta: Gypsy Moth Parasites 47
This subspecies was first mentioned by Howard and Fiske (1911) asa
native North American parasite of the gypsy moth. According to them the
record of Theronia melanocephala (Brullé) = hilaris hilaris (Say) of Forbush
and Fernald (1896) pertained to this subspecies. They considered it a pri-
mary parasite of the gypsy moth. It has been also reared from Itoplectis
conquisitor (Say), another primary parasite of the gypsy moth, which often
fails to develop on that host. They believed it to be a case of superparasitism:
the host pupa by chance containing larva of [toplectis and Theronia parasitizing
that pupa. JT. atalantae fulvescens is parasitized by a chalcid, Dibrachys
cavus.
Theronia atalantae fulvescens differs from the nominate subspecies by
having the flagellum black to brownish-black, mesopleurum largely yellow,
usually without fuscous markings, though in larger specimens sometimes
present on prepectus near lower corner of pronotum, and wings hyaline,
lightly tinged with yellow. Specimens from southwestern U.S.A. tend to have
wings a little darker.
This subspecies is sometimes difficult to separate from atalaniae atalantae,
as coloration of the two often approach each other.
Length: 6-13 mm. Fore wing 4-11 mm.
Specimens: U.S.A.: Providence, R.I., 1%, July 24, 1916, ''ex tray of
b.t. pupae", Gypsy Moth Lab., No. 12099. 2%, August 6, 1907, Gypsy Moth
Lab., No. 826-07 (Hamden). Perry Co., Pa., Millers Gap, ex pupa, 1¢,
June 27, 1978, E. M. Blumenthal. Dauphin Co., Pa., Jackson Twp., July 6,
1977 (both these apparently reared from Lymantria dispar ) (Pennsylvania).
Distribution: Widely distributed in North America. Schedl (1936) mentioned
it as occurring in Japan, but that record should pertain to T. atalantae gesitator.
Hosts: Several host records are given by Townes (1940) and Carlson (1979).
Townes and Townes (1960) give several biological references.
Biological Notes: Howard and Fiske (1911) considered Theronia atalantae
fulvescens as "the most common American parasite completing its transfor-
mation upon the gypsy moth" pupae. Parasitism at times amounted to 2 per
cent. It appears that the adult female overwinters and that there is a single
generation per year.
According to the observations of Campbell (1963), this species seeks its
host under shady conditions, in forests and seldom is seen in the open, though
at times it may be seen along the border of a defoliated area. About 25% of
the pupae stung by the parasite produced ichneumonid offspring. None of the
pupae stung were fed upon, but all prepupae stung were fed upon. The effec-
tiveness of this parasite is both by parasitization as well as by killing the
host pupae and prepupae through stinging.
Townes (1940) summarized the biological information on this species as
follows:
"Theronia atalantae may be either a primary or a secondary parasite. If
the host attacked has already been parasitized by another ichneumonid it
becomes a secondary parasite, if not it lives as a primary. There is no clear
evidence that it is obligated to be a secondary parasite on any host, although
it has been shown usually to live thus in the case of Malacosoma. Asa pri-
mary parasite the insect lives inside its host. When it is a secondary para-
site, it lives inside its primary host and outside of its secondary host. The
egg is deposited only in a prepupa or a freshly formed pupa. Fiske believes
the egg stage to last about a day. He has observed that on the average the
first three larval stages last two days each and the fourth stage feeds for two
days and then spins its cocoon for one day and rests two days before forming
48 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
the pupa. After two to four days the pupa hatches. Development from the egg
to the adult thus consumes fourteen to eighteen days. When a secondary para-
site on Malacoma americana (through Itoplectis conquisitor) in New Hampshire,
most of the adults emerged July 10-20, the females about four days behind the
males. Itoplectis conquisitor emerged from the same cocoons on an average
of seven days earlier than its parasite. "
1c. THERONIA ATALANTAE GESTATOR (Thunberg)
Ichneumon gestator Thunberg, 1822. Mem. Acad. Imp. Sci. St.
Pétersbourg, 8: 262; 1824, 9: 312.
Theronia japonica Ashmead, 1906. Proc. U. S. Natl. Mus., 30: 181.
Japan.
Theronia japonica: Howard and Fiske, 1911. U.S. Dept. Agr. Bur.
Ent. Bull.,91: 121. Japan. Host: Lymantria dispar .
Theronia atalantae gestator: Townes, Momoi and Townes, 1965. Mem.
Amer. Ent. Inst., 5: 64. Synonymical and biological references.
Japan, Korea, China, USSR.
This subspecies is readily distinguished from the other subspecies of
atalantae by having dark brown bands or spots on its abdomen, and the thorax
also extensively dark marked. The wings are pale-hyaline, flagellum brown,
hind coxa with a black or dark brown mark, and the hind femur is often fus-
cous ventrally. |
The Japanese and the Korean populations of this subspecies are uniformly
distinctive by the blackish markings, but populations from USSR and China
tend to intergrade with atalantae atalantae. Rarely the American specimens
approach gestator by having black markings on basal abdominal tergites or
somewhat extensively on the thorax.
Length: 8-13 mm. Fore wing 5.5-11.5 mm.
Specimens: Japan: 4%, 32, bred from Lymantria dispar, 1908, 1910,
‘some without date, Gypsy Moth Lab., Nos. 1600, 1825, & 3399A (Hamden).
1%, labelled ''Europe ex L. dispar, Istria Austria thru Ruhl, Gypsy Moth Lab.
No. 853-07, Au. 12. 07.'' (Hamden). Japan: Sekigahara, Honshu, 2°, 19.
ex pupa of Lymantria dispar, June 20, 1977, emerged July 6, 7 and 10, 1977,
P. Schaefer (B.I.R.L., Delaware).
Distribution: Eastern Palaearctic Region, typically in Japan, Korea,
North China, Siberia and adjacent areas. Occurrence in Europe (specimen
from Austria above) is rather unusual, though it is reported to intergrade
with atalantae atalantae in Europe.
This subspecies was first reported as a parasite of Lymantria dispar by
Howard and Fiske (1911). Further references are given by Townes, Momoi and
Townes (1965).
1d. THERONIA ATALANTAE HIMALAYENSIS, n. subsp.
(= Theronia sp., or Theronia atalantae atalantae from Lymantria
obfuscata from Kashmir) |
Male and female: This subspecies is characterized by its brownish wings,
black flagellum, and rufous brown body, with fuscous marks on antennal
scrobes, prepectus, below subtegular ridge, base of scutellum, wing bases,
lower half of mesopleural groove, and along groove separating metapleurum
V. Gupta: Gypsy Moth Parasites 49
from mesopleurum. The anterior margin of the middle lobe of mesoscutum
rather vertically and conspicuously raised and prominently separated from the
rest of mesoscutum. In profile view the front edge of mesoscutum appears
concave and raised. Ventral margin of hind femur with a shorter ridge, incon-
spicuously serrated.
Length: 10-13 mm. Fore wing 9-11.5 mm.
Holotype: 2, India: Manali, 1828 m., in Northwest Himalaya (Himachal
Pradesh), May 29, 1970, Dauli Ram, Coll. No. K252 (Gupta). Pavatypes:258,
same locality as the holotype, collected between May 17 to June 3, 1970 by
various collectors (Gupta). Kashmir: Srinagar, 1%, 1%, July 1966, ex pupa
of Lymantria, Gupta, No. 277; 12, June 1970, Gupta (Gupta). Srinagar, 4°,
49, July 1963, C. I. B. C., Indian Station, ex pupae of Lymantria obfuscata
on willow (CIBC, Bangalore).
This subspecies has earlier been determined as Theronia atalaniae ata-
lantae: (Poda), or simply as Theronia sp. (Rao, 1966, 1972). The following
information on the biology of this subspecies is summarized from those
reports:
Adults of Theronia atalantae himalayensis appeared in the middle of June
in Srinagar. The females were seen flying over the congregations of pupae of
Lymantria obfuscata in search of suitable hosts. Freshly formed pupae were
Oviposited upon. In the laboratory freshly emerged adults paired immediately
and mating lasted 8-15 minutes. The ratio of males to females was 1:2.
The egg is cream colored, elongate with one end narrower than the other,
and measures about 2 mm. in length. It is laid in the body cavity of the pupa.
The larva hatches in three days and starts feeding soon after. Once the para-
site larva inside the host pupa is active, the latter stops all movements after
about two days and becomes hard and stiff. The full grown parasite larva is
yellowish in color and measures about 12-14 mm. in length and 3 mm. in
width. It is tapering at the caudal end. Because of the developing parasite,
the host turns slightly blackish between the fourth to ninth abdominal segments.
The full grown larva spins a cocoon which forms a lining to the abdominal wall
of the host. The parasite pupa is also yellowish in color. The adult parasite
genaws an irregular hole and comes out. Males emerge earlier than the
females and are generally smaller in size.
The total life-cycle from the egg to the adult takes about 21-24 days.
This subspecies does not appear to show any preference for any particular
ecological condition or host plant. In general the percentage parasitism varied
from 2% to 20%, although Rao (1972) recorded as high as 40. 82% parasitism
in a Salix plantation and stated that 'It was a constant mortality factor operating
against the pupae of L. obfuscata in all the four experimental localities. "'
Rao (1972) made some observations on the emergence of the moths from
pupae that were pricked by T. atalantae himalayensis (as well as other pupal
parasites). It was observed that the adult parasite fed on the host haemolymph
after every prick. When freshly formed pupae were pricked either once or
thrice, more parasites emerged than from 4-5 day old pupae pricked. The
mortality of the pupae increased with increasing number of pricks. The moth
emergence was greater when 4-5 day old pupae were pricked by the parasite,
particularly after a single prick.
Rao (1966) also reported that, ''on one occasion, 4 parasite larvae were
found feeding externally on a fourth instar larva of L. obfuscata and one of them
developed to adult stage in June 1963. "'
20 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
2. THERONIA HILARIS HILARIS (Say)
Ichneumon hilaris Say, 1829. Contrib. Maclurean Lyceum Arts Sci.,
1: 41..U. 5S. 4.
Pimpla melanocephala Brullé, 1846. Hist. Nat. Insectes Hymén., 4: 99.
North America. Name preoccupied.
Theronia melanocephala: Fernald, 1892. Bull. Hatch. Exp. Sta. Mass.
State Coll., 19: 116. Massachusetts. Host: Lymantria dispar.
Theronia melanocephala: Viereck, 1917. Bull. Conn. Geol. Nat. Hist.
Survey, 22: 323. Hosts: Lymantria dispar and others.
Theronia hilaris: Townes and Townes, 1960. U.S. Natl. Bull., 216(2):
356.
Theronia hilaris hilavis: Carlson, 1979. In Krombein et al.: Catalog of
Hymenoptera in America. . ., 1: 347
This subspecies was first mentioned (as T. melanocephala) by Fernald
(1892) as a parasite of the gypsy moth in Massachusetts, U.S.A. Forbush
and Fernald (1896) called it ''the most abundant of the hymenopterous para-
sites" in 1895. Howard and Fiske (1911), however, considered that the record
of T. melanocephala of Forbush and Fernald was actually of T. fulvescens
[=atalantae] and that ''the true T. melanocephala appears not to have been
reared from this host. '' Campbell (1963) observed both Theronia hilaris
(= melanocephala) and T. atalantae, attacking the gypsy moth in Glenville,
N.Y. He, however, did not discuss hilaris further in that paper. It, there-
fore, appears that it is just an occasional parasite of the gypsy moth.
This subspecies is readily distinguished from atalantae by nothaving a
ridge along the ventral margin of the hind femur and by its black head. It
differs from the Eurasian subspecies of hilaris by its rufous thorax and abdo-
men. T. hilaris laevigata (Europe) and T. hilaris nigra (Japan and Siberia)
are wholly black. The legs of laevigata are largely reddish, while those of
nigvya are wholly black.
No reared specimens from the gypsy moth have been seen. It is widely
distributed in eastern and midwestern North America. Townes and Townes
(1960) provides a detailed description and distributional data and Carlson
(1979) records the hosts of T. hilaris hilavis.
Tribe PIMPLINI
Members of the tribe Pimplini are distinguished from the other tribes of
Pimplinae by having a uniformly convex mesoscutum, without wrinkles, pre-
pectal carina present, mesopleural suture with an angulation just above middle,
propodeum without transverse carinae, often median carinae present at base
and pleural carinae complete, tarsal claws of female, at least the front claws,
nearly always with a basal tooth, areolet present (except rarely), nervellus
intercepted variously, first tergite with a glymma, first sternite separate
from first tergite, with dorsolateral carinae, subgenital plate of male trans-
verse, with its apex truncate or retuse, and ovipositor long to very long,
slender and of a uniform diameter.
The coloration is generally black. The pattern on hind tibia is rather
characteristic, with apical and subbasal dark bands and median area and
extreme base of tibia pale yellow.
Members of the Pimplini genera treated below are external parasites of
V. Gupta: Gypsy Moth Parasites ol
late larvae of various Lepidoptera that have just spun their cocoons, or those
living in leaf rolls, etc. The development is completed upon the host larva
within the cocoon. Two genera, Acropimpla and Iseropus are associated with
the gypsy moth. Gregopimpla is treated here as a subgenus of Iseropus.
5. Genus ACROPIMPLA
Acropimpla Townes, 1960. U. S. Natl. Mus. Bull., 216(2): 159.
Townes (1969: 84) and Gupta and Tikar, (1976: 128) may be consulted for
generic synonymy and affinities of the genus.
Some of the salient features of the genus are:
Body moderately long and slender, clypeus of male, and often the face
of male white or yellow. Malar space very short to almost wanting. Face usu-
ally with its upper margin raised and often narrowly and strongly, or broadly
cleft. Occipital carina complete, dipped a little on the mid-line above. Pro-
podeum rather short and convex, with or without median longitudinal carinae.
Areolet triangular, oblique, usually short petiolate, receiving second recurrent
vein at its outer corner (sometimes the areolet lacking). Nervellus intercepted
below middle. First tergite short and wide, its median dorsal and dorsolateral
carinae rather strong. Second tergite with short, moderately strong oblique
erooves cutting off its basolateral corners. Third and fourth tergites with
distinct tubercles. Ovipositor straight, compressed, usually nearly as long
as fore wing, but shorter in some species, its apex usually slender, seen in
profile, concave above and the ridges on the tip of its lower valve very oblique.
Acropimpla is predominantly Oriental; but it also occurs in the Holarctic
and Ethiopian regions. Their known hosts are several species of Microlepi-
doptera.
1. ACROPIMPLA DIDYMA (Gravenhorst)
Pimpla didyma Gravenhorst, 1829. Ichneumonologia Europaea, 3: 178.
Europe.
Acropimpla didyma: Oehlke, 1967. Hymenopterorum Catalogus (novo
editio),2(1): 15. Host: Lymantria dispar.
This Species was reported as a parasite of Lymaniria dispar for the first
time by Sedivy (1963) from Czechoslovakia, as Ephialtes didymus (Graven-
horst).
Female: Face polished, centrally raised, its upper margin straight.
Mesoscutum hairy, subpolished. Mesopleurum and metapleurum polished and
shiny, with scattered setiferous punctures. Propodeum with faint median
carinae at base, which are somewhat divergent apically. Propodeum smooth
dorsally, its pleural area with scattered punctures. Abdomen with coarse and
scattered punctures. Tubercles on tergites punctate. Ovipositor long, as long
as the fore wing.
Black. Face with an inverted crescentic yellow mark just below antennal
sockets. Hind corner of pronotum, tegula, and wing bases, yellow. Legs
yellowish-brown, with apical 0.3 of hind tibia, and tarsus except at extreme
base, blackish.
Male: Generally similar to the female, but face more convex and with
scattered punctures. Face and clypeus wholly yellow. Scape yellow ventrally.
Hind margin of pronotum also yellow. Fore and middle legs more yellowish,
lighter in coloration than the hind leg.
52 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Length: 8mm. Fore wing 6 mm.
Specimens and distribution: Several males and females from Europe
examined in the Townes Collection. No reared specimens were seen. It is
widely distributed in Europe. ; :
Hosts: Lymantria dispar (vide Sedivy, 1963), and various other hosts
belonging to the families Lasiocampidae and Noctuidae as mentioned by
Sedivy (1963) and Aubert (1969).
This species runs to Group B and to Acropimpla varuna Gupta and Tikar
from Java in the Gupta and Tikar (1976) Monograph on Oriental Pimplini.
The two species are rather close. A. varuna, however, is distinguished by
having a yellow scape in the female and the mesopleurum with a red mark in
the dorsal half. The other European species of the genus, A. pictipes (Graven-
horst) is black, without yellow marks on face, and the propodeum and abdomen
are coarsely sculptured.
6. Genus ISEROPUS (Figs. 5, 6,130, 131)
Iseropus Foerster, 1868. Verh. Naturh. Ver. Rheinlande, 25: 164.
Gregopimpla Momoi, 1965. Mem. Amer. Ent. Inst., 5: 601. [Subgenus
of Iseropus].
Body moderately slender and long. Clypeus of female black to yellow.
Clypeus convex, its apical margin thin and with a median notch. Malar space
short. Occipital carina complete, with a moderate dip medially above. Pro-
podeum moderately convex, with median longitudinal carinae. Areolet present.
Nervellus intercepted at or above the middle. First tergite short and wide,
its dorsal and lateral carinae strong. Basolateral oblique grooves on second
tergite moderately strong to obsolete. Third and fourth tergites with tubercles,
their impunctate bands occupying about 0.2 their length. Ovipositor straight,
compressed, its apex slender, concave above, the ridges of basal teeth very
oblique. Ovipositor 0.5 to 0.8 as long as the fore wing.
Two subgeneraare recognized:Iseropus (Iseropus) and Iseropus (Grego-
pimpla). Diagnostic characters are mentioned in the key that follows. Mem-
bers of the genus are gregarious parasites of lepidopterous prepupae in thin
cocoons, particularly of the families Lymantriidae, Lasiocampidae and
Notodontidae.
Further taxonomic information may be obtained from Townes (1969) and
Gupta and Tikar (1976). Information on larval morphology and affinities is
provided by Short (1978).
Three species have been associated with the gypsy moth. They are
Isevopus (Iseropus) stercorator Fabricius (= Pimpla holmgreni Schmiede-
knecht), Iseropus (Gregopimpla) himalayensis (Cameron) (= Iseropus hakonensis
Ashmead) and Iseropus (Gregopimpla) inquisitor (Scopoli).
KEY TO THE SUBGENERA AND SPECIES OF ISEROPUS
ASSOCIATED WITH THE GYPSY MOTH
1. Interocellar distance 0.8 as great as ocellocular distance. Second tergite
with conspicuous basolateral grooves. Abdominal tergites only moder-
ately punctate, with shiny areas in between the punctures. Areolet as
high as wide, more triangular in outline with second recurrent vein
close to its middle. Face of male white. (Subgenus Jseropus).
1. stercorator Fabricius
V. Gupta: Gypsy Moth Parasites D3
Interocellar distance 1.25 as great as ocellocular distance. Second tergite
with faint to indistinct basolateral grooves. Abdominal tergites wholly
rather densely punctate. Areolet wider than high, more rectangular,
with second recurrent vein close to its outer corner. Face of male
black,:: (Subsehus Gre gopinpl i V6 Big SAO te NG 2
2. Face and metapleurum impunctate and shiny. Side of thorax shiny.
Female flagellum 24-27 segmented. Median propodeal carinae extend-
ing up to 0.7-0.8 the length of propodeum. Propodeum evenly convex.
Tergite 2 without oblique grooves. Legs slender, reddish, with hind
tibia banded with fuscous and hind tarsus black except basally. Stigma
pale Drow? Vis 80s Gai se VST iin GPS ee Aes 2. inquisitor (Scopoli)
Face and metapleurum with coarse scattered punctures. Side of thorax
with scattered punctures. Female flagellum 29-30 segmented.
Median propodeal carinae confined to basal 0.5-0.6 of propodeum.
Propodeum more convex in profile. Tergite 2 with faint oblique grooves.
Legs a little thicker with bands on hind tibia rather conspicuously black
and coxae and trochanters yellow marked. Stigma blackish-brown.
3. himalayensis (Cameron)
1. ISEROPUS (I.) STERCORATOR STERCORATOR (Fabricius) (Figs. 5, 131)
Ichneumon stercorator Fabricius, 1793. Entomologia Systematica, 2: 172.
Germany.
Ichneumon graminellae Schrank, 1802. Fauna Boica, 2(2): 301.
Czechoslovakia.
Pimpla Mussii Hartig, 1838. Jahresber. Forstschr. Forstwiss. Forstl.
Naturk., 1: 253. Germany.
Pimpla Holmgreni Schmiedeknecht, 1888. Zool. Jahrb. System., 3: 448,
002. Germany.
Iseropus stercorator Roman, 1912. Zool. Bidr. Fran Uppsala, 1:280.
Iseropus stercorator Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5:29. syn., ref., distr., hosts, etc. Eurasia, Japan.
Iseropus stercorator Fab. in older literature was used as a senior synonym
of flavipes Gravenhorst or a junior synonym of inquisitor Scopoli. It has also
been cited as stercovatory Gravenhorst. It appears that the host records are
mixed up because of this confused nomenclature.
Rudow (1911) reported it as a parasite of Lymantria dispar and L. monacha,
but in 1917 recorded only monacha as its host. Stadler (1933), Schedl (1936)
and Thompson (1946) report it as a parasite of the gypsy moth under the name
Pimpla holmgreni. No Lymantria hosts are mentioned by Oehlke (1967) or
Aubert (1969).
The association of Iseropus stercorator with Lymantria dispar has not
been confirmed by recent rearings.
Iseropus stercorator orgyiae (Ashmead) is the Nearctic subspecies.
Female and male: Face punctate, smoother along eye orbits and near
base of clypeus. Clypeus subpolished, convex in basal half. Malar space
short, 0.2 to 0.25 the basal width of mandible. Frons and vertex smooth,
subpolished. Interocellar distance a little less than ocellocular distance
(8:10). Mesoscutum hairy, subpolished with shallow indistinct punctures.
Scutellum convex subpolished. Pronotum minutely punctate and with a smooth
central area. Mesopleurum convex, polished, with minute punctures in the
4 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
prepectal area. Metapleurum polished and with a few scattered minute punc-
tures. Propodeum largely smooth but the scattered punctures and rugosities
at places, not convexly sloping, its median carinae divergent and extending
only in the basal 0.5 of propodeum. Areolet triangular. First recurrent vein
equal to the second. Nervellus intercepted at its upper 0.3. First tergite
thinner, smoother laterally. Abdominal tergites with irregularly formed
punctures with shiny interspaces. Swellings on tergites tending to be smoother.
Oblique grooves on second tergite sharper. Ovipositor compressed, about
0.6-0.7 as long as the fore wing and the abdomen.
Female: Color black. Flagellum, clypeus and palpi brownish. Legs
reddish-brown. Hind tibia with broad black subbasal and apical bands. Hind
tarsal segments black in apical half (or more). Stigma and veins brown.
Hind femur without fuscous mark. Tegula brown with a yellow anterior spot.
Male: Face, clypeus and scape ventrally, yellow. Fore and middle coxae
with yellow spots. Otherwise like the female.
No reared specimens seen. Several European specimens examined in the
Townes Collection.
Distribution and hosts: This subspecies is widespread in Europe and also
occurs in Japan and eastern Russia. Several hosts have been reported by
Aubert (1969: 42) belonging to the families Curculionidae, Tortricidae,
Ypnomeutidae, Oecophoridae, Gelechidae, Pyralidae, Zygaenidae, Lasio-
campidae, Notodontidae, Lymantridae, and Noctuidae. He does not mention
any Lymantria species as host.
Iseropus (I1.) stercorator stercorator is rather close to the Nearctic
stercorator orgyiae (Ashmead), and coelebs (Walsh) and also to the Japanese
orientalis Uchida. I. stercovrator orgyiae differs from the nominate subspe-
cies in having a black apical mark on the hind femur, white tegula, and rougher
propodeum with longer median carinae. J. coelebs has denser punctures on
the pronotum, mesopleurum and metapleurum, and elongate male claspers.
Townes and Townes (1960) provide additional distinguishing characters.
I. orientalis has pale labial palpi, pale tegula, black hind coxa and hind femur
lightly fuscous apically. The side of thorax is shiny, with a few scattered
punctures. The propodeum is more like that of orgyiae and coelebs.
2. ISEROPUS (GREGOPIMPLA) INQUISITOR (Scopoli) (Figs. 6, 130)
Ichneumon inquisitor Scopoli, 1763. Entomologia Carniolica Exhibens
Insecta Carnioliae Indigena, p. 286.
Pimpla inquisitoy Stadler, 1933. Ent. Anz., 13: 30.
Gregopimpla inquisitor Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5:27. Eurasia. Host records after Meyer, 1934.
For further synonymical references refer to Oehlke (1967) and Aubert
(1967).
The first report of this species (as Pimpla inquisitor) from gypsy moth
could be traced only to Stadler (1933). The only other record is by Vasic
(1958) from Yugoslavia. As mentioned under J. stercorator, the present
species has been confused in the past with stercovator and it is not sure
which of the two, if ezther, is really parasitic on the gypsy moth.
Aubert (1969) gave an elaborate list of hosts belonging to the following
families of Coleoptera, Lepidoptera and Hymenoptera: Anobiidae,
Curculionidae, Tortricidae, Cochylidae, Yponomeutidae, Pyralidae,
Geometridae, Lasiocampidae, Lymantriidae, Noctuidae, Cephidae, and
Tenthredinidae. He listed Lymantria monacha as a host after Brischke, 1878
V. Gupta: Gypsy Moth Parasites o5
(Brischke cited Pimpla stercorator 'Gravenhorst' % = flavipes). He did not
mention L. dispar as a host of this species. Oehlke (1967) did not mention
any Lymantria hosts.
Male and female: Flagellum 24-27 segmented. Face smooth and shiny.
Clypeus subpolished, not strongly convex. Interocellar distance a little more
than the ocellocular distance (8:7). Frons and vertex smooth. Temple a little
more convex than in himalayensis. Head in dorsal view quadrate. Mesoscu-
tum subpolished, shiny, and with scattered punctures. Scutellum with
scattered punctures and shiny. Pronotum polished. Mesopleurum and meta-
pleurum polished and with scattered punctures. Propodeum evenly convex,
its median carinae more parallel-sided and extending up to 0.7-0.8 the length
of propodeum. Propodeum with shallow rugosities across middle. Nervellus
intercepted at the middle or at upper 0.45. Areolet 1.5 as wide as high. Legs
slender. Hind femur about 5.4 as long as wide. First tergite slender, its
median carinae making an angle of 309 with the horizontal. Whole of abdomen
densely punctate. Apical smooth bands on tergites a little wider than in hima-
layensis. Second tergite without grooves. Ovipositor about 0.85 as long as
fore wing. |
Black. Pedicel and basal flagellar segments ventrally yellowish. Palpi,
hind corner of pronotum, and tegula yellow. Legs reddish-brown, with tibiae
and tarsi a little paler. Hind tibia with conspicuous black bands. Hind tarsus
black with basal 0.3 to 0.4 of first segment yellow. Stigma pale brown. In
male, the fore and middle legs largely pale yellow and scape and pedicel
yellow ventrally.
Specimens: Several males and females from Europe examined in the
Townes Collection. No reared specimens seen.
Distribution and relationships: Iseropus (G.) inquisitor is distributed in
Eurasia. It is close to I. kuwanae Viereck from Japan and is distinguished
from the latter by having the hind tarsal segments largely black, first tergite
slender, abdomen coarsely punctate, and propodeum being evenly convex. It
differs from J. himalayensis by having a smoother face and metapleurum,
slender hind femur, and median propodeal carinae extending up to 0.7 the
length of propodeum.
3. ISEROPUS (GREGOPIMPLA) HIMALAYENSIS (Cameron)
Pimpla himalayensis Cameron, 1899. Mem. & Proc. Manchester Lit.
Phil. Soc., 43(3): 178. India.
Epiurus hakonensis Ashmead, 1906. Proc. U. S. Natl. Mus., 30: 179.
Japan.
Pimpla japonica Ulbricht, 1911. Soc. Ent. Stuttgart, 26:54. Japan.
Preoccupied. Host: Samia cynthia pryevi.
Epiurus satanus Morley, 1913. Fauna British India, Hymenoptera,
$(1): 173. India.
Itoplectis attaci Habermehl, 1917. Ztschr. f. Wiss. Insektenbiol., 13: 117.
New name for Pimpla japonica Ulbricht.
Epiurus quersifoliae Uchida, 1928. J. Fac. Agr. Hokkaido Imp. Univ.,
25: 59. Japan. Host: Gastropacha quercifolia.
Itoplectis attaci: Kamiya, 1934. Bull. Forst Exptl. Sta. Govt.-Gen.
Chosen, 18: 66. Japan. Hosts: Dendrolimus spectabilis,
Lymantria dispar (first record).
Gregopimpla himalayensis: Townes, Momoi and Townes, 1965. Mem.
Amer. Ent. Inst., 5:26. China, India, Japan, Korea. Host records,
o6 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
synonymical references.
Male and female: Flagellum 29-30 segmented. Face punctate below
antennal sockets, smoother along inner orbits and near clypeus. Clypeus
subpolished. Malar space 0.2 the basal width of mandible. Interocellar dis-
tance a little more than ocellocular distance (10:8). Frons and vertex
polished, shiny. Mesoscutum elongate, leathery in texture. Scutellum with
shallow punctures apically. Side of thorax shiny, polished with scattered
shallow punctures on pronotum and mesopleurum. Metapleurum with more
definite punctures than mesopleurum. Punctation on metapleurum similar to
that on face. Propodeum roundly convex, its median carinae confined to its
basal 0.5, diverging apically and ending in a rugose band across propodeum.
Basolateral areas of propodeum with scattered but definite punctures. Legs
short, not slender. Hind femur 4.5 as long as wide. Nervellus intercepted
at upper 0.4. Areolet elongate 1.5 to 2.0 as wide as long. First tergite
short, convex, with sharp evenly arched median carinae, which may be a little
angled medially. Second tergite without conspicuous basolateral grooves.
Whole of abdomen densely punctate, only apices of tergites smoother. Ovi-
positor about 0.8 the length of fore wing.
Black. Antenna yellowish-brown ventrally. Maxillary palpi, tegula, and
hind corner of pronotum, yellowish-brown. Legs brownish with yellowish-
brown patches on fore and middle coxae, femora, and tibiae. Hind tibia with
conspicuous fuscous sub-basal and apical bands, clearly separated by a wide
yellow area. Hind tarsus blackish but first tarsal segment yellow on basal
0.5-0.6. Bases of other tarsal segments yellow.
Specimens examined: Several males and females from India and Japan in
Townes and Gupta Collections. In the Townes Collection, a specimen bears the
following data: 'Emerged from pupa of Lymantria dispar on 5-VI-1930",
"Kyushu, Fukuoka (Chikuzen)."
Distribution: Widespread throughout the northern belt of the Oriental Region
(Northern India, China, Japan, and Korea).
Hosts: Lymantria dispar, and several other hosts in Japan and India
[Townes, Townes & Gupta (1961) and Townes, Momoi & Townes (1965). |
Kamiya (1934) first reported it from the gypsy moth (as Itoplectis attaci) in
Japan.
Iseropus (G.) himalayensis is close to the Palaearctic I. (G.) bernuthii
(Hartig) in having similar punctuation of face, metapleurum, shorter hind femur
and hind tibia distinctly banded (which characters separate these two from the
other species of the subgenus Gregopimpla). I. (G.) bernuthii, however, is
different from himalayensis in having parallel median propodeal carinae, pro-
podeum rugose only in central area between carinae, propodeum dorsally flatter,
and the fuscous bands on hind tibia not separated by a clear pale band.
Il. SUBFAMILY PORIZONTINAE
Members of the subfamily Porizontinae are characterized by having an
apically compressed abdomen, with spiracle placed behind the mid-length of
first tergite. Clypeus usually not distinctly separated from face. Mandibular
teeth usually equal. Notauli absent. Sternalus absent or short. Propodeum
partly to completely areolated. Tarsal claws usually pectinate. Areolet
present or absent—when areolet absent, intercubitus basad of second recurrent
vein (except in Hellwigiini). Epipleurum of tergites 2-3 separated by a crease.
V. Gupta: Gypsy Moth Parasites oO”
Subgenital plate transverse, not enlarged. Male clasper usually rounded
apically. Ovipositor long or short, with a subapical dorsal notch and lower
valve without teeth. |
They are usually small sized species. They are usually primary internal
parasites of lepidopterous larvae, except for some genera which parasitize
larvae of Coleoptera, Rhaphidiidae or Tenthredinidae.
Six genera have been associated with the gypsy moth. They are
keyed below:
KEY TO THE TRIBES AND GENERA OF PORIZONTINAE
ASSOCIATED WITH THE GYPSY MOTH
1. Cross-section of petiole near its basal third depressed oval or circular.
Suture separating its sternite from tergite at or above the mid-height,
the suture always present. First tergite without a pit (glymma) before
spiracle, sometimes a lateral groove may be present.
(Por momtind) o wisseis: Waierks aca hi ity ccna Ss Oh aie Me a wees 2
Cross-section of petiole near its basal third quadrangular or prismatic;
suture separating its tergite from sternite below the mid-height, the
suture present or obsolete. First tergite with or without a pit before
ite. spiracles (MRR ie tile cd haus) ai hes tate Aneel ane 4
2. Pronotum narrow with a deeper groove. Epomia long and strong, almost
reaching upper margin of pronotum. Propodeum narrowed towards
apex, without carinae (except at base). Eyes distinctly emarginate just
above antennal sockets. Ovipositor hardly exerted, as long as the apical
COI OT MICO OM deja! Bilas ta tee aN eens pew at lps 3. Casinaria
Pronotum broad with a shallow groove in the middle. Epomia short, not
extending to upper margin of pronotum. Propodeum short, not narrowed,
apically, more convex in profile, with distinct transverse and longitu-
dinal carinae. Ovipositor long, 0.5 to 1.0 as long as the abdomen.
EVGA WERKIY COVBTOUATR, cick Voin ser Ce ee BOR A MR EG 3
3. Postpetiole broad, parallel-sided, flatter dorsally and with a lateral
carina extending from spiracle to its apex. Basal part of petiole pris-
matic and flattened above. Frons with a weak median vertical carina.
Combined areola and petiolar area of propodeum forming a broad, deep
concave trough,
BE AAC Maia ae ly ak RL HE SEAR ROIS wa UN lig iia, Sle: Eee yaad
Postpetiole narrower, more globular in profile, without a lateral carina
between spiracle and its apex. Petiole basally more cylindrical or
depressed-oval. Frons with or without a median carina. Areola usually
constricted posteriorly and the median trough not very deep.
pi yA Pha hila Tide in EA epee eal an 2 - 2. Campoplex
4. Nervellus intercepted, though discoidella unpigmented. Areolet receiving
second recurrent vein basad of its middle. Apical margin of clypeus with
a short median tooth, which is sometimes rather weak. Glymma pre-
OTs i Wiech emp cnatind la Wa AA Ae ha beh tt Sia to 4. Campoletis
Nervellus not intercepted. Areolet receiving second recurrent vein at or
distad of the middle. Clypeus without any median projection. Glymma
PPOSON OF MOONE ih Mis RTA iar PRU OE Am ih dam CN ee as 5)
08 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
o. Nervulus distad of basal vein by about 0.3 its length, strongly sloping to
make an angle of about 70° with the discoidal vein. Clypeus rather wide,
flat and with its apical margin truncate. Petiole without a conspicuous
lateral pil or Slymmas oi eo a a Do. Phobocampe
Nervulus interstitial or only slightly distad of basal vein, almost vertical
or slightly arched. Clypeus short and convex. Petiole with a distinct
lateral pit-orclymmiag 4.) ae YS ee ee 6. Hyposoter
1. Genus SINOPHORUS (Fig. 43)
Sinophorus Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 153.
For taxonomical and synonymical references refer to Townes (1970) and
Gupta and Maheshwary (1977).
Small sized insects, about 6-11 mm. long. Body stout. Fore wing 3 to 8
mm. long. Clypeus large and flat with apical margin weakly rounded and
truncate. Mandible with a ventral lamella. Malar space 0.43 to 0.56 as long
as the basal width of mandible. Frons with a weak median vertical carina.
Eye weakly emarginate. Pronotum broad, with a shallow groove. Epomia
short, not extending to upper margin of pronotum. Propodeum short, with
areola and petiolar area completely confluent and forming a broad deep con-
cave trough. Median longitudinal carinae of propodeum widely separated.
Areolet present. Second recurrent vein inclivous. Nervellus usually not
intercepted, the base of discoidella usually detached from nervellus. Petiole
prismatic basally, the suture separating the tergite from sternite distinct and
a little below the mid-height. First tergite without a lateral pit or glymma,
but often with a shallow long groove. Postpetiole broad, parallel-sided, flat-
ter dorsally and with a lateral carina extending from spiracle to its apex.
Apex of male clasper rounded. Ovipositor about 1.7 to 2.1 as long as the
hind femur.
Members of the genus Sinophorus are internal parasites of lepidopterous
larvae or sometimes sawflies. This genus has not yet been certainly associated
with the gypsy moth and the records in the literature appear erroneous.
1. SINOPHORUS VALIDUS (Cresson) (Fig. 43)
Ruhl (1914) reported Limnerium validum Cresson (type-species of
Sinophorus) as a parasite of Lymantria dispar in the U.S.A. on the authority
of Timberlake (1912). Timberlake was working on the biology of L. validum,
which is a parasite of Euproctis chrysorrhoea, and attempted to rear it on
Lymantria dispar, but failed. Subsequent cataloguers like Stadler, Schedl,
and Thompson, mentioned it as a parasite of the gypsy moth in Europe and
North Africa—on whose authority is not clear.
Fusco and Simons (1973) mentioned S. validus as an unimportant native
parasite of the gypsy moth found in association with the tent caterpillar and the
webworm. Simons etal, (1979), quoting Carlson (1973, personnal corre-
spondence) mentioned that this species had been reared from the gypsy moth,
but only rarely. However, Carlson (1979: 625) does not list L. dispar asa
host of this species, and states, "I have listed only hosts from labels of
specimens which I have identified as validus. Some of the host records in
literature pertain to misidentifications in USNM collections."
V. Gupta: Gypsy Moth Parasites 59
It is thus evident that all records of this parasite ex gypsy moth are
erroneous.
2. Genus CAMPOPLEX (Fig. 44, 134)
Campoplex Gravenhorst, 1829. Ichneumonologia Europaea, 3: 453.
For full synonymical and other references, refer to Townes (1970) and
Gupta and Maheshwary (1977).
Body slender. Small-sized insects about 3-11 mm. long. Fore wing 2-8
mm. long. Clypeus weakly convex, its apical margin rounded, sometimes
truncate, usually weakly depressed in the middle. Mandible with a ventral
lamella, which is often weak. Malar space 0.4 to 0.8 as long as the basal
width ofmandible. Frons without a median carina, except rarely. Eye not
or only weakly emarginate. Pronotum broad, with a shallow groove. Epomia
short. Propodeum with its median longitudinal carinae somewhat closer (cf.
Sinophorus) and angulate at the junction of areola and petiolar area—these
two areas confluent but the junction between them discernible. Areola and
petiolar area forming a flat, weakly depressed or a little excavated area, and
not in the form of a broad deep trough. Areolet present, stalked or weakly
sessile. Sometimes areolet absent. Second recurrent vein slanting outward.
Nervellus usually intercepted. Petiole usually cylindrical in cross-section in
basal 0.3, sometimes a little squarish. Postpetiole more globular in shape,
usually wider in the middle, and somewhat raised in profile, without any
lateral carina. Suture separating first tergite from sternite distinct and at
middle or a little below middle. Glymma absent, but in its place usually a
narrow, shallow groove present. Apex of male clasper broad and round, or
sometimes with a shallow apico-dorsal emargination. Ovipositor 1.5 to 4.1
as long as the hind femur.
Ratzeburg (1844) recorded two species of Campoplex as parasites of the
gypsy moth, viz., Campoplex difformis Gravenhorst and C. conicus Ratzeburg.
The latter species is a synonym of Casinaria tenuiventris (Gravenhorst). The
identity of the species reported as C. difformis is uncertain, as according to
several authors it has been a mixed and often misidentified species. Perhaps
two different species, C. difformis and Venturia deficiens were involved, but
the true identity of the species reared from the gypsy moth can only be
decided when voucher specimens or freshly reared material turns up.
Campoplex deficiens Gravenhorst (= algerica Habermehl) is a species of
Venturia (Horstmann, 1974). It is not discussed further.
Campoplex vapax Gravenhorst, as reported in the gypsy moth literature
(Rudow, 1911) appears to be a species of Hyposoter. It has been referred to
subsequently under Anilasta or Anilastus.
Momoi (1961) reported Campoplex sugiharai (Uchida) from Lymantria
dispar in Japan.
Campoplex sp. of Burgess and Crossman (1929) is actually Casinaria
tenuiventris (Gravenhorst).
Kolemietz (1958) reported Omorgus sp. as a parasite of the pupa of the
gypsy moth, reared in August 1955 in Siberia. Omorgus is a synonym of
Campoplex, the species of which are internal parasites of lepidopterous larvae,
spinning their own cocoon after killing the host larva or prepupa and emerging
from their own cocoons.
60 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
KEY TO THE SPECIES OF CAMPOPLEX ASSOCIATED
WITH THE GYPSY MOTH
1. Face rugulose. Abdomen wholly black. Hind femur, tibia and tarsus
yellowish-brown. Occipital carina joining hypostomal carina at the
base of mandible. Propodeal areola well formed in both the sexes,
though widely open behind. Europe....... 1. difformis (Gmelin)
Face granulose. Abdomen reddish-brown laterally. Hind femur, tibia
and tarsus blackish-brown to light brown. Occipital carina joining
hypostomal carina just above the base of the mandible. Propodeal areola
not well formed in the female, its median longitudinal carinae absent
below costulae and weakly represented apically. Japan, Korea, Ryukyus,
Thailand and’southeré India... ee 2. sugiharai (Uchida)
1. CAMPOPLEX DIFFORMIS (Gmelin) (Fig. 134)
Ichneumon difformis Gmelin, 1790. Jz Linnaeus: Systema Naturae,
Ed. 13 1 (5): 2,720. des. Type destroyed. (Neotype 2, designated
by Horstman (1969), the same specimen as the lectotype of
mutabilis Holmgren).
Campoplex difformis: Gravenhorst, 1829. Ichneumonologia Europaea,
3: 458. Europe. (A mixed series).
Limneria mutabilis Holmgren, 1860. Svenska Vetensk. Akad. Handl.
(N.F.) 2(8): 55. Lectotype °, labelled and designated by Hinz (1964,
Entomophaga, 9: 70), Sweden: Smaland (Stockholm).
Campoplex difformis Gravenhorst: Ratzeburg, 1844: 92. Host: Lymantria
dispar (vide Bouché, Garten Ins., p. 154).
Horstman (1969) has shown that the true Campoplex difformis Gravenhorst,
which is actually Campoplex difformis (Gmelin), is a senior synonym of
Campoplex mutabilis (Holmgren), and that what most authors have called
"Campoplex difformis Gravenhorst" is the same as Venturia deficiens Graven-
horst. Aubert (1975) rejects the neotype fixation of difformis by Horstman and
considers difformis and mutabilis as different species. According to him the
present species should be called mutabilis Holmgren, and deficiens Graven-
horst = algerica Habermehl, should be called difformis (Gmelin).
Whether true difformis (Gmelin) as described below is a parasite of
Lymantria dispar or not, can only be ascertained by fresh rearings.
Male and female: Face rugulose. Clypeus, frons, and vertex granular.
Malar space 0.6 the basal width of mandible. Interocellar distance 1.4 the
ocellocular distance. Temple and vertex granuloso-mat. Occipital carina
joining hypostomal carina at base of mandible. Mesoscutum granulose, tending
to be rugose at places. Mesopleurum and metapleurum granulose, with a few
scattered punctures. Scutellum granulose. Propodeum granulose in basal
areas, transversely striate in apical half, particularly in petiolar area. Pro-
podeal carinae rather strong, including the lateral longitudinal carina (which
is weaker in other species). Areola wide, as wide or wider than the length of
costula, rather widely open behind. Areola and petiolar area forming a rather
wide trough as is usually seen in Sinophorus. Postpetiole finely granulose.
Abdomen mat. Ovipositor as long as or a little shorter than the fore wing and
longer than the abdomen.
V. Gupta: Gypsy Moth Parasites 61
Black. Mandible often partly brownish. Tegula yellow. Coxae black.
Legs otherwise reddish-brown. Hind trochanters blackish-brown. Hind tibia
and apex of hind femur fuscous. Tegula brown in the male.
Length: 6-7 mm. Fore wing 4.5to 5mm. Ovipositor 4.0 mm.
Specimens from Europe examined in the Townes Collection. No reared
Specimens seen.
2. CAMPOPLEX SUGIHARAI (Uchida)
Omorgus sugihavrai Uchida, 1932. Trans. Sapporo Nat. Hist. Soc.,
12:74. Japan.
Campoplex sugiharai: Momoi, 1961. Kontyt, 29: 272. Japan, Korea.
Host: Lymantria dispar.
Campoplex sugihavai: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 276. Japan, Korea. Momoi, 1970. Pacific Insects,
12: 383. (Key and description of two subspecies from Thailand
and Ryukyus). Gupta and Maheshwary, 1977. Ichneumonologia
Orientalis, 4: 79.
This parasite has not been previously cited in the gypsy moth literature.
It has the abdomen reddish-brown laterally and hind femur, tibia and tarsus
blackish-brown to light brown. It occurs in the Orient and Japan.
Male and female: Face, frons, and vertex granulose. Clypeus finely
granulose. Malar space 0.5 the basal width of mandible. Interocellar distance
1.0 to 1.2 as long as the ocellocular distance. Temple and occiput finely
granuloso-mat. Occipital carina joining hypostomal carina a little above the
base of mandible. Mesoscutum and scutellum strongly granulose. Pronotum
granuloso-striate. Mesopleurum and metapleurum granulose, metapleurum
more finely and densely so. Propodeum granulose. Petiolar area apically
trans-striate. Basal transverse carina and the short carinae bounding basal
area, the strongest. Areola not formed infemale. Median longitudinal carinae
erased, visible only in the apical half and enclosing a moderately deep trough-
like petiolar area. Apical transverse carina visible laterally. In male median
carinae joining basal transverse carina so that the areola is formed laterally.
Areola a little constricted apically and widely confluent with petiolar area.
Second lateral area and petiolar area of propodeum trans-rugulose. Hind
coxa, and first and second tergites granulose. Petiole without a lateral pit or
groove before spiracle, but with a fine lateral carina from base to the spiracle.
Thyridium on second tergite small, oval and separated from base of second
tergite by about 2.5 its length. Abdomen from third tergite onwards mat.
Ovipositor long, about as long as the abdomen, 0.8 to 0.9 as long as the fore
wing, evenly arched upwards.
Black. Mandible, palpi, and tegula partly or wholly, yellow. Fore and
middle legs largely yellowish-brown, with their coxae often brownish to
blackish. Hind coxa black. Hind leg otherwise dark brown with tibia centrally
light brown. Abdomen brownish-black to black, with third and the following
tergites yellowish-brown. Antenna brownish black to black.
Length: 7-9mm. Fore wing 4 to 5.5mm. Ovipositor 3.5 to 4.5 mm.
Momoi (1970) recognized three subspecies: C. sugiharai sugihavai (Uchida)
from Japan and Korea, C. s. okinawensis Momoi from Ryukyus (Okinawa) and
C. s. australis Momoi from Ryukyus (Omotodake) and Thailand. The three
subspecies differ in the coloration of scape and pedicel (light brown to black
62 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
beneath), hind first trochanter (light brown to black), middle coxa (brown to
black), tergites 3-8 (reddish-brown to black laterally), and hind femur (light
reddish-brown to blackish-brown).
Specimens from Japan and Korea examined in the Townes Collection. No
reared specimen seen.
A specimen from Naduvattom, S. India in the Townes Collection, agrees
with this species, but comes somewhat in between sugthavai sugiharvai and
sugtharai australis.
Distribution and hosts: Momoi (1961) reported it as a widespread species
in Japan and Korea and recorded Lymantria dispar as a host in Kyushu,
Japan.
This species comes close to Campoplex burmensis Gupta and Maheshwary
(1977) from Burma and C. oriens Gupta and Maheshwary from the Orient. It
differs from the former in having a long ovipositor and areola not formed in
the female. It differs from oviens in having blackish hind femur, and short,
almost parallel-sided basal area.
3. Genus CASINARIA (Fig. 45, 135)
Casinaria Holmgren, 1859. Ofvers. Svenska Vetensk. Akad. Forh.,
15: 325.
For full synonymical references, refer to Townes (1970). The Oriental
Species were treated by Gupta and Maheshwary (1977), and the Nearctic
species by Walley (1947).
Body slender, with fore wing 4 to9 mm. long. Eye margin strongly
indented opposite antennal socket. Cheek short. Temple moderately short to
very short and flat. Mesopleural suture, or at least its median 0.3,
impressed as a sharp groove. Pronotum narrow, with epomia complete.
Propodeum moderately long to very long, its apex between basal 0.3 and the
apex of hind coxa. Propodeum usually with a median longitudinal trough, with
incomplete areolation, or without carinae. Propodeal spiracle short, elongate-
oval. Fore wing with areolet always present. Second recurrent vein usually
inclivous. Nervellus not intercepted. Petiole cylindric or weakly depressed,
moderately long to very long, the suture separating its sternite from tergite at
or a little above the mid-height. Postpetiole a little bulbous. Glymma absent.
Apex of male clasper rounded or a little elongate, without a subapical dorsal
notch. Ovipositor short, 0.8 to 1.4 as long as the apical depth of abdomen,
notched subapically.
This is a large genus of world-wide distribution. They are parasitic
within lepidopterous caterpillars.
Two species of Casinaria are generally reported as parasites of the larvae
of Lymantria dispar, viz., Casinaria tenuiventris (Gravenhorst) (= Campoplex
tenuiventyis Gravenhorst = Campoplex conicus Ratzeburg) and C. ischnogaster
(Thomson). The record of the latter species is erroneous. Momoi (1963)
added Casinaria anastomosis Uchida to the list of gypsy moth parasites in
Japan. It is a junior synonym of Casinaria nigripes (Gravenhorst).
Morley and Rait-Smith (1933) recorded Casinaria ischnogaster as a para-
site of Lymantria dispar on the authority of Morley (1914, Ichn. Britain,
5: 112). In the latter reference, Morley clearly states that records of the
"synonymous Campoplex conicus from Bombyx dispar (Ratz., 1: 95), should
be referred to Gravenhorst's species [ tenuiventris], which Thomson also calls
V. Gupta: Gypsy Moth Parasites 63
C. latifrons Holmgr.' He, infact, did not record C. ischnogaster as a para-
site of Lymantria dispar and was only clarifying the identity of 7schnogaster
vs. tenuiventris in the British fauna. C. ischnogaster is therefore to be
removed from the list of gypsy moth parasites.
In literature two species of Casinaria, viz., C. claviventris Holmgren
and C. scutellaris Tschek are reported as parasites of Lymantria monacha,
the nun moth in Europe.
KEY TO THE CASINARIA SPECIES PARASITIC UPON THE GYPSY MOTH
1. Abdomen wholly black. All coxae and trochanters black. All femora
and tibiae reddish-brown (except rarely the hind femur blackish).
Burpe; UGSRe 6. i ae 1. tenuiventris (Gravenhorst)
Abdomen with at least tergites 3 and 4 red. Middle and hind legs almost
wholly blackish, their tibiae lighter in basal half. Japan, Europe,
USSR. euc ko aoe ee ee 2. nigripes (Gravenhorst)
1. CASINARIA TENUIVENTRIS (Gravenhorst) (Figs. 45, 135)
Campoplex tenuiventris Gravenhorst, 1829. Ichneumonologia Europaea,
3: 482. Poland.
Campoplex conicus Ratzeburg, 1844. Die Ichneumonen der Forstinsecten,
1:95. Germany. Host: Lymantria dispar. (Syn. by Dalla Torre,
1901-02: 126).
Casinaria latifrons Holmgren, 1858. Svensk. Vetensk. Akad. Handl.,
(2) 2(8): 50. (cf. Dalla Torre, 1901-02).
Casinaria tenuiventris: Brischke, 1880. Schrif. Naturf. Ges. Danzig,
N.F. 4 (4): 147. |
Campoplex sp. Burgess and Crossman, 1929. U.S. Dept. Agr. Tech.
Bull., 86: 104. Larval parasite. France, Czechoslovakia.
For fuller synonymical references, see Dalla Torre (1901-02), Morley
(1914), Meyer (1935), and Townes, Momoi and Townes (1965). Dalla Torre
misspelled Campoplex conicus as C. canonicus Ratz. Howard and Fiske
(1911) reported C. tenuiventris as a parasite of gypsy moth larvae, though the
earliest record would be that of Ratzeburg (1844), as Campoplex conicus. I
have examined specimens from France and Czechoslovakia that were men-
tioned by Burgess and Crossman as Campoplex sp.; these belong to the present
species. In recent years, it has been mentioned as having been reared from
the gypsy moth in Yugoslavia (Vasic, 1958), Russia (Shapiro, 1956) and Iran
(Herard et al., 1979)
Male and female: Face almost squarish, rugulose. Clypeus narrow,
slightly convex, granulose, its apical margin convex and impressed. Mandible
short and broad, with a wide lower lamella. Malar space 0.75 to 0.85 as long
as the basal width of mandible. Temple strongly receding behind eye. Head
lenticular. Frons granulose, without a median carina. Interocellar distance
1.4 as long as ocellocular distance. Lateral ocellar diameter about equal to
ocellocular distance. Occipital carina strong, sinuate below lower level of
eye and meeting hypostomal carina at the base of mandible. Mesoscutum con-
vex, finely rugose. Scutellum rugulose, slightly convex with its lateral carinae
confined to its front 0.4. Mesopleurum and metapleurum granuloso-rugulose.
64 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Pleural area of propodeum more strongly sculptured than metapleurum,
generally finely rugose. Dorsal face of propodeum rugose with a shallow and
broad median groove along its length, which is beset with short transverse
carinae. Propodeum coarser in male than in female, particularly in the median
trough and areas laterad to it. Propodeum narrowed apically and extending to
the basal 0.33 of hind coxa. Propodeal spiracle elongate-oval. Hind coxa
granulose. Areolet moderate-sized, short petiolate, receiving second recur-
rent in the middle. Nervellus not intercepted, reclivous. First tergite 1.2
as long as the second, shorter than the hind femur. Abdomen not strongly
compressed, clavate or rounded apically. Male claspers broader and
rounded apically. Ovipositor short, straight, hardly exerted beyond the tip of
abdomen. Ovipositor sheath a little clavate.
Black. Tegula black to yellowish-brown. Coxae and trochanters black.
Legs otherwise reddish-brown with tarsi and apical 0.3-0.5 of hind tibia lightly
fuscous. Sometimes hind femur and tibia dark, brownish or black, with tibia
faintly banded. Abdomen wholly black. Middle femur may have basal black
marks.
Length: 6-8 mm. Fore wing 3-4 mm.
Specimens: Germany: Wurzburg, 1°, June 1974, ex Lymantria dispar.
France, 1°, June 1981, ex Lymantria dispar (BIRL, Newark). France
[Hyeres], 1°, ex Lymantria dispar, V-28-1922, Gypsy Moth Lab No. 3438
(FIS. Hamden, Ct.) Czechoslovakia, Bilky, 1925, ex Lymantria dispar, No.
3475, 1° 1¢ (Hamden, Ct.), 1% 12 (USNM), 1° 12 (Townes). Bulgaria, 1924,
ex Lymantria dispary (Hamden, Ct.) France: Foret des,May-June 1972-73,
3°, ex gypsy moth larvae (EPL, Paris). Poland: Skiern., 12, June 1975, ex
gypsy moth larva (EPL, Paris). China: Heilongjiang Province. Several
males and females, reared from larvae of Lymantria dispar and L. mathura
by Schaefer, ef al. in May-June 1982.
Distribution: Europe, China, Iran (Herard etal., 1979).
This species belongs to the Atrata Group of Gupta and Maheshwary,
1977. The specimens from China have the hind femur wholly black. It comes
close to C. natashae Maheshwary & Gupta from the Himalaya.
Kolemietz (1958) mentioned rearing Casinaria tenuiventris (Gravenhorst)
from gypsy moth larvae in Siberia during August 1954. It was considered
rare. Pschorn-Walcher (1974) reported it (plus another species "red" =
nigripes) from Southern France, Austria and Bavaria as an uncommon or
rare parasite of young as well as of older larvae of the gypsy moth. The
larval head of this species is figured by Short (1978).
Casinaria ischnogaster, wrongly reported as a gypsy moth parasite is
close to C. claviventris in leg color and general body sculpture, but the
head is not so lenticular, propodeum broad and short, rugose dorsally, and
with its median groove shallow. The postpetiole is dilated at the level of the
spiracle, then narrowed apically. In C. claviventris the outer posterior
angle of discoidal cell is slightly obtuse, and the radial cell shorter and
broader. C. scutellaris is unknown to me. The latter two species have been
reported parasitic upon Lymantria monacha.
~
2. CASINARIA NIGRIPES (Gravenhorst)
Campoplex nigripes Gravenhorst, 1829. Ichneumonologia Europaea,
3: 598. Poland.
Casinaria nigripes: Thomson, 1887. Opuscula Entomologica, 11: 1102.
V. Gupta: Gypsy Moth Parasites 65
Casinaria anastomosis Uchida, 1930. Insecta Matsumurana, 4: 130.
Japan: Sapporo. New synonym. Host: Ichthyura anastomosis.
Fuller synonymical references to the two species can be found in Townes,
Momoi and Townes (1965: 279). Momoi (1963: 54) first reported Lymantria
dispar as a host of anastomosis in Japan. A recently bred specimen of this
species from the gypsy moth in France is at hand.
Other host records are: Ichthyura anastomosis, Orgyia gonostigma,
O. thyellina and Epicnaptera ilicifolia in Japan; and Dasychiva pudibunda,
Orgyia antiqua, Dendrolimus pini, and D, sibiricus in USSR. Its hyperpara-
sites are Itoplectis alternans in Japan and USSR, and Gelis areator, Gelis Sp.,
Pteromalus sp., and Theronia atalantae in USSR.
This species is readily distinguished by the red color of central abdominal
tergites and blackish hind leg.
Male and female: Essentially similar in sculpture to C. tenuiventris and
differing as follows:
Lateral ocellus separated from eye by about 0.7 its diameter. Interocellar
distance 1.8 the ocellocular distance in female and about 2.0 inmale. Malar
space 0.5 to 0.7 the basal width of mandible. Areolet large, with a short
petiole. First tergite 1.3 as long as propodeum, thinner than in tenuiventris ,
less widened apically. Propodeum somewhat coarser dorsally, particularly
in male. In male median groove trans-carinate and lateral areas reticulate.
Both petiolar area and lateral areas with irregular longitudinal incomplete
carinae. Body sculpture coarser, tending to be finely rugose, particularly
face, meso- and metapleurum.
Abdomen with apex of tergite 2 and tergites 3 and 4 wholly red. (Tergite
5 also red in one specimen before me.) Legs black with fore femur reddish
and fore tibia and tarsus yellowish. Middle tibia and tarsus often yellowish-
brown, particularly in male, and middle femur may also be brownish-yellow
apically. |
Length: 8-10 mm. Fore wing 5-7 mm. Larger than C, tenuiventris,
Specimens: S. France, 1°, May-June 1972, ex gypsy moth larvae (EPL,
Paris). Japan: Sapporo, 1°, compared with type of C. anastomosis (Townes).
Germany: 30, 3¢ det. as C. nigripes by Heinrich and by Teunissen (Townes).
China: Heilonjiang Province, several %, °, ex Lymantria mathura, May-June
1982, P. Schaefer et al. (BIRL, Delaware).
Distribution: Europe, USSR, China, Japan.
Hosts: Lymantria dispar, L. mathura, and others, as mentioned above.
Pschorn-Walcher (1974) reported this as ''Casinaria sp. red'' from
France, Austria and Bavaria as an uncommon parasite of the larvae of the
gypsy moth, together with C. tenuiventris. He also referred to both of them
collectively as "'Casinaria spp."
4. Genus CAMPOLETIS (Fig. 46)
Campoletis Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 157.
For full synonymical references, refer to Townes (1970). Anilastus and
Anilasta are junior synonyms of Campoletis, although in older literature
Anitlastus has been incorrectly but rather consistently used for Hyposoter.
This was because of the misidentification of the type-species of Anilastus,
Small sized species with fore wing 3.3 to 7.5 mm. long. Body moderately
66 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
slender. Eyes weakly emarginate. Malar space small. Clypeus moderately
wide, weakly to moderately convex, its apical margin with a median tooth of
varying shape and size. Sometimes the tooth indistinct. Propodeal areola
usually elongate, hexagonal, distinct from petiolar area or more or less fused
with it. Areolet short petiolate, or pointed above, receiving second recurrent
vein basad of its middle. Nervellus intercepted, discoidella unpigmented.
First abdominal segment moderately decurved, with a moderately slender
petiole and moderately stout postpetiole. Suture separating tergite from
sternite below the mid-height of petiole. Glymma present. Thyridium sub-
circular, separated from base of tergite by 0.7 to 1.5 its diameter. Oviposi-
tor moderately stout, upcurved or almost straight, 1.6 to 3.5 as long as
apical depth of abdomen.
Species of Campoletis have been occasionally collected from the larvae
of the gypsy moth, recently in China (P. Schaefer) and France (EPL, Paris).
Their specific identities are uncertain.
Species reported in the literature under Anilastus or Anilasia, like
Anilastus rapax (Gravenhorst), or Anilastus n. sp. Stadler (1933) appear to
belong to Hyposoter. Their specific identity is uncertain in the absence of
the reared specimens. The figure of the larval remains in Stadler (1933)
corresponds to that of H. tricoloripes (Viereck), which is known from Europe.
Two specimens of Campoletis bred from the gypsy moth in France are at
hand. They are described below as Campoletis sp., because it is probable
that the species has a name in Europe, but the name is unknown to me.
CAMPOLETIS sp.
Male: Face granuloso-punctate. Face and clypeus forming a convex sur-
face, without a clear demarcation. Apical margin of clypeus convex and with a
median acute tooth, which is rather well developed. Malar space about as
wide as the basal width of mandible. Ocellar area punctate. Interocellar
distance 1.4 the ocellocular distance. Ocellocular distance equal to ocellar
diameter. Temple subconvex, not receding from eye. Thorax largely granu-
lose. Areola granulose, open behind, a little constricted at its junction with
petiolar area. Costula distinct. Petiolar area striate, subconcave and
widened medially. Propodeal carinae more or less complete. Petiole and
postpetiole finely granulose. Glymma in the form of a deep pit. Tergite 2
more than twice its basal width, mat. The following tergites subpolished.
Black. Mandible, palpi, fore and middle legs, pale yellowish-brown.
Tegula yellow. Hind femur orange brown. Tibia whitish-yellow medially and
base of hind tarsus yellowish-white. Second and following tergites reddish-
brown laterally. Second and third also with faint reddish apical irregular
bands. ;
Length: 5.5-6mm. Fore wing 4 mm.
Specimens: South France, 2%, May-June 1973 (EPL, Paris).
Cocoon: Silken white, slender, cylindrical, about 3.0 as long as its
medial diameter.
5. Genus PHOBOCAMPE (Figs. 48, 136)
Phobocampe Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 156.
For full synonymical references, etc. refer to Townes (1970: 175).
Body short, with fore wing 4to 6mm. long. Eye margin weakly or not at
V. Gupta: Gypsy Moth Parasites 67
all indented opposite antennal sockets. Cheek short. Clypeal foveae not dis-
tinctly impressed, open. Clypeus weakly convex, with a subapical groove, the
apex sharp, truncate or subtruncate. Mandible short, with a fringe on its
lower margin, its teeth equal. Temple rather short. Occipital carina joining
hypostomal carina. Lower corner of pronotum translucent. Mesopleurum mat
to granulose. Posterior mesosternal carina complete, though often weak.
Propodeum short, its areola and petiolar areas confluent or with a small con-
striction at their junction. Costula present. Propodeal spiracles circular or
oval. Hind basitarsus without a ventral row of closely spaced hairs. Tarsal
claws short and pectinate. Fore wing with areolet petiolate above, receiving
second recurrent vein distad of its middle. Nervulus distad of basal vein by
about 0.3 its length, strongly slanted, forming an angle of about 70° with the
discoidal vein. Discoidella unpigmented, usually not reaching nervellus.
Nervellus vertical and usually not intercepted. Petiole slender. Postpetiole
rather broad. Suture separating sternite from tergite a little below the mid-
height of petiole. Glymma small to obsolescent. Abdomen short and stout.
Thyridium circular, separated from base of second tergite by about its di-
ameter. Ovipositor about as long as the apical depth of abdomen, with a sub-
median notch.
The hosts are small or early instar lepidopterous caterpillars.
Viereck (1911) described Hyposoter disparis (now Phobocampe unicincta)
as a parasite of gypsy moth larvae received in the U.S.A. from Russia.
Howard and Fiske (1911) mentioned that they were first received in 1907 ina
shipment of small gypsy moth caterpillars from Kiev, Russia. This parasite
was subsequently released in Northeastern United States and has become
established. It has, however, proved to be of little value in the control of
the gypsy moth.
Burgess and Crossman (1929) mentioned having received specimens of two
distinct species of Hyposoter in addition to disparis from Europe (Spain,
Czechoslovakia, Hungary and Yugoslavia) during 1924, 1925 and 1927. The
adults of these emerged from the cocoons in the same season in which they
were formed, rather than hibernating in cocoons and issuing the following
spring, as was the case in disparis. They also pointed out that such adults
did not mate and oviposit and that "it seemed that they might hibernate. They
were placed in several types of containers for hibernation, but the last one
died after living 92 days. '' About the same specimens Muesebeck (1933)
remarked, ''Hyposoter disparis is easily confused with an unidentified species
of the same genus which is occasionally reared as a parasite of the gypsy-
moth larvae in Europe. The latter differs, however, in having the antennae
28-30 segmented; in the ocellocular line being slightly shorter than the di-
ameter of an ocellus; in the less erect areolet of the anterior wing, with the
second recurrent joining the cubitus very near the second intercubitus; and in
having the petiolar area wider and uniformly closely granular and opaque. "'
The majority of these specimens represent a new species, Phobocampe
lymantriae, while some from Hungary are P. unicincta. There are some
variations in the two, which occur sympatrically in many areas in Europe.
Both of them also occur in Japan.
Shapiro (1956) listed Phobocampe pulchella Thomson as one of the ichneu-
monid parasites of Lymantria dispar in Russia. Drea (in Doane and McManus,
1981: 31) also mentions P. "pulchella Thomson" as a parasite of the gypsy
moth from Yugoslavia. This species is rather close to P. unicincta, but is a
different species (lectotype examined). I suspect that the species involved
might be either of the two European species of Phobocampe discussed here.
68 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
The record of Herard et al. (1979) of Phobocampe sp. from the gypsy moth
in Iran concerns P. unicincta. A specimen of this material, now in Washing-
ton, has been examined. The record of Drea and Fuester (1979) of Phobocampe,
n. sp. from Poland apparently pertains to P. lymantriae, which is sympatric
with unicincta. Specimens collected by Fuester, located in Washington, have
also been examined.
KEY TO THE PHOBOCAMPE SPECIES ASSOCIATED
WITH THE GYPSY MOTH
1. Tergite 2 yellow or orange in apical half, sometimes this may be narrow
(0.5 to 0.33); in males much narrower. Tergite I, often apically
yellow infemale. Postpetiole parallel-sided, laterally not distinctly
margined, as long as or longer than wide. Propodeal areola usually
constricted below costula, and median longitudinal carinae usually
distinct. Areola and petiolar areas with transverse striations.
Malar space 0.5 to 0.7 the basal width of mandible. Interocellar
distance 1.3 to 1.5 the ocellocular distance. Ocellocular distance
longer than ocellar diameter (rarely equal). Europe, USSR, Japan,
Bnd USAG Ct SS AR eee Fa 1. unicincta (Gravenhorst)
Tergite 2 narrowly yellow apically (0.25-0.3); in male often without yellow
band or only apicolaterally faintly yellow. Tergite I hardly yellow.
Postpetiole rather sharply constricted from petiole, distinctly margined
and convex laterally, wider than long, widest submedially. Propodeal
areola not fully formed, not constricted, widely open below. Areola
and petiolar areas granulose. Malar space 0.25-0.4 the basal width of
mandible. Interocellar distance 1.7 to 1.9 the ocellocular distance.
Ocellocular distance slightly shorter than ocellar diameter. Europe,
daa, USA Oe a ee Oe. 2. lymantriae, new species
1. PHOBOCAMPE UNICINCTA (Gravenhorst) (Figs. 49-51, 57-62, 136)
Campoplex unicinctus Gravenhorst, 1829. Ichneumonologia Europaea,
3: 529. ¢. (% misdet.).
Hyposoter disparis Viereck, 1911. Proc. U. S. Natl. Mus., 40: 478.
i : Henin USSR] "Gypsy moth Lab." Synonymized by Carlson
1979).
Limnerium disparis: Howard and Fiske, 1911. U. S. Dept. Agri. Bur.
Ent. Bull., 91: 121, 191. Japan. Russia. Host: Lymantria dispar.
Phobocampe disparis: Townes, 1945. Mem. Amer. Ent. Soc., 11: 646.
Phobocampe unicincia: Carlson, 1979. In Krombein et al.: Catalog of
Hymenoptera in America North of Mexico, 1: 661. Syn. Introduced
in U. S. A.
Biological references: Howard and Fiske (1911), Burgess and Crossman
(1929), Muesebeck and Parker (1933), Schedl (1936).
This species has so far been referred to as Phobocampe disparis or
Hyposoter disparis and has only recently been synonymized under P. unicincta
by Carlson (1979), after examining the types of unicincta and dispavis.
This species was first discovered in the gypsy moth laboratory in Massa-
chusetts in 1907 from a small collection of gypsy moth caterpillars imported
from Kiev, Russia. In 1911 it was found in great abundance at Gioia Tauro,
V. Gupta: Gypsy Moth Parasites 69
Italy. The cocoons of it gathered from Italy were shipped to Massachusetts and
adults that emerged the following spring (1912) were liberated around Melrose
Highland. It was recovered from the field in 1913. It has apparently been
recovered each year but only in small numbers. It has established itself in
the U.S.A. but has not been able to exert much influence on the population of
the gypsy moth.
Male and female: Antennal flagellum usually 28-32 segmented. Face
strongly granulose. Clypeus finely granulose, its apical margin impressed and
straight. Malar space 0.5 to 0.7 the basal width of mandible, a little wider in
male than infemale. Frons granulose. Vertex finely so. Interocellar distance
smaller, 1.3 to 1.5 the ocellocular distance. Ocellocular distance longer than
ocellar diameter. Temple and occiput subpolished and receding from the eye.
Mesoscutum coarsely granulose. Scutellum finely granulose. Propleurum,
mesopleurum and metapleurum granulose, but granulations finer than that of
mesoscutum. Granulations on propleurum and speculum a little sparser and
these areas somewhat shiny. Pronotal groove and prespecular area with
carinations. Granulations on metapleurum somewhat similar to that of meso-
scutum. Propodeum granulose in basolateral areas. Areas apicad of basal
transverse carina with coarse granulations. Petiolar area and areola trans-
carinate, more so in female than inmale. Sometimes males with granular
areola. Propodeal carinae in general strong. Basal transverse carina usually
strongly angled medially. Areola a little constricted apically (though open), its
lateral carinae a little convergent or parallelsided and then widely diverging.
Sometimes these carinae weak or obliterated just below costulae. Areola more
flat and petiolar area a little concave. Propodeal spiracle oval, connected to
pleural carina by a strong carina equal in length to the spiracular opening.
Areolet small, petiolate with second recurrent vein emitted from its middle.
Nervulus inclivous, distad of basal vein by about 0.3 to 0.33 its length, making
an angle of 60° with the submedian vein. Discocubitus strongly arched. Petiole
quadrate basally, a little flattened apically, gradually merging with the postpeti-
ole. Postpetiole finely to coarsely granulose, parallel-sided, longer then wide
or almost squarish. Postpetiole laterally not margined, the lateral carina thin
or weak. Lateral groove of petiole weak. Tergite 2 narrower, elongate,
more so in male, about 2.0 as long as its basal width in female and more than
2.0 inmale. Thyridium irregularly round, separated from base of second ter-
gite by a distance a little less than its maximum diameter. Spiracle of second
tergite at its middle. Abdomen dull mat. Ovipositor as long as the apical
depth of abdomen, or a little longer, finely tapered and slightly upcurved.
Ovipositor sheath a little clavate apically. Female subgenital plate appears
more hairy. Epipleurum of tergite IV with uniformly distributed hairs, not
clustered along its margin.
Black. Mandible, palpi, fore and middle trochanters, and tegula, yellow.
Scape and pedicel ventrally, hind corner of pronotum, fore and middle legs
largely, and hind trochanters, yellowish. Sometimes fore and middle coxae,
tibiae and trochanters more yellow than brown. Hind coxa and femur reddish-
brown, tibia yellow to yellowish-brown and tarsus brownish. Apex of hind
coxa, apex of femur, base and apical 0.25 of tibia, and tarsal segments api-
cally infuscate. Apex of postpetiole narrowly, thyridia and apical 0.33 to 0.95
of second tergite yellow to reddish-brown. In males yellow on first tergite
absent. Second tergite apically usually amber colored or only narrowly or
laterally yellowish-brown. |
The propodeum exhibits some variations. Usually the areola and petiolar
area are demarcated by a constriction and both have irregular carinations in
70 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
addition to granulations. Sometimes lateral carinae of areola are weak and
areola may be more granular. But the nature of postpetiole, malar space and
ocellocular distance in conjunction with the propodeal sculpture and the width
of the yellow band on second tergite will distinguish it from the related
Phobocampe lymantriae, n. sp. The males often have granular areola but they
usually have faint or narrow apical band on second tergite and the malar space
is larger than in the female. Other distinguishing characters also hold good
for the male.
Length: 4to 7mm. Fore wing 3.5 to 5 mm.
Specimens: 30°, 502, from: Italy [Gioia Tauro] April-May 1912. Vees,
Hungary, May 1929. Var and Bouches du Rhone, France, May-June 1973.
S. France, June 1972, May 1973. France, June 1980. Prilep, Yugoslavia,
May-June 1973. Jovljak, Yugoslavia, May-June 1973. Trenton, Mass.,
U.S.A., May 1948. Lancaster Co., Pa., U.S.A., May 1977. Hawk Mts.,
Pa., May 1974. Mohonk Lake, N.Y., May, 1974, all reared from Lymantria
dispar. Glenville, N.Y., June 1960. High Point State Park, N. J., May
1973. Starkoc. Boh., Czechoslovakia, July 1961 (not reared).
In addition, the following specimens also belong to this species: North
Iran, Location A, 1°, May 5-14, 1976, ex Lymantria dispar, Herard &
Mercadier, EPL-Iran-76-2 (Washington). This has the postpetiole a little
wider apically. Japan: Hokkaido: Hobetsu, 1°, 12, June 15, 1978. ex
Lymantria dispar, P. Schaefer, emerged Nov. 1978 (Washington). 3°, Japan
"APL-78-18C'"' and APL-77-26" (BIRL, Newark). 1°, Eniwa, Hokkaido, June
3, 1977, reared, Herard. Honshu, Utsunomiya, 1°, June 3, 1978, ex
Lymantria dispar (BIRL, Newark).
The specimens from Japan labelled ''APL-78-18C"' and "APL-77-26" are
typical untcincta, while the other specimens from Japan have somewhat less
striate propodeum, hind femur is blackish, and the band on second tergite is
narrow. They match with wnicincta rather than with lymantriae in most of
the characters. These have been previously labelled or mentioned as
"Phobocampe n. sp."
Cocoon: Cocoon uniformly dark brown in color, 6x4mm., oval. Some-
times blackish-brown.
Distribution: Europe, USSR, Iran, Japan, and U.S.A. (Introduced).
This species is widespread in Europe and has definitely been established in
northeastern United States. Pschorn-Walcher (1974) reported Phobocampe
unicincta (= disparis) to be a dominant parasite of the gypsy moth in Wirzburg,
Germany, subdominant in eastern Austria, and of moderate abundance in
southern France. Earlier, Burgess and Crossman (1929: 49) reported that it
was scarce in Russia during their search in 1909-1910, but was found abun-
dantly in Gioia Tauro, Italy in 1911. Muesebeck and Parker (1933) reported
that specimens of this species have been received from various localities in
Austria, Czechoslovakia, Poland, Hungary, Yugoslavia, Bulgaria and Italy.
It appears to be most abundant in south-central Europe. In the United States
it was recovered by them from Northeastern Massachusetts and Eastern United
States. Since then it has been recovered from Pennsylvania, New Jersey and
New York.
BIOLOGY
Phobocampe unicincta is a specific univoltine, internal parasite of
Lymantria dispar. Parasitism is generally low, although on occasions heavy
V. Gupta: Gypsy Moth Parasites 11
parasitism has been observed in different parts of Europe. Apparently the
parasitism is heavier in dense woodland than in open growth or on the outer
edges of wooded areas. Muesebeck and Parker (1933) published on the biology
of this species (as Hyposoter disparvis). The following information is sum-
marized from their paper:
Phobocampe unicincta, which was released in the areas of the New England
states infested with the gypsy moth in 1912 onwards, has definitely become
established, but has remained of little value as a control factor. Some of the
factors that contribute to its ineffectiveness, are heavy hyperparasitization,
much overwintering mortality, and much loss of the egg and first-instar larvae
due to phagocytosis.
About 12, 500 adults were liberated for the first time in four localities in
eastern Massachusetts and one point in southeastern New Hampshire, in the
spring of 1912 that were reared out of cocoons received in 1911 from Gioia
Tauro, Italy. Importations ceased between 1912 and 1920. During 1924-1931
small numbers of the parasite were received from Hungary and Yugoslavia,
and three small colonies were liberated in the field in Massachusetts during
that time.
Collections of gypsy moth larvae were made at all the five points of 1912
release and the parasite recovered from each point.
Hibernation: Phobocampe unicincta hibernates as an adult within the cocoon.
The posterior end of the body remains immersed in the moist meconial dis-
charge. If the meconium dries, the parasite dies within the cocoon. In the
field the cocoons remain on the surface of the ground throughout the winter,
usually covered by leaf litter.
Emergence and mating: The adult unicincta emerges at about the time
when eggs of the gypsy moth begin to hatch, usually in late April and early
May. Temperatures of 65°F. or higher stimulate mating and sunlight is
essential. Most satisfactory mating was obtained in the laboratory when
freshly emerged females were mated with 3-4 day old males.
Oviposition: Females oviposit readily into the first and second instar lar-
vae of the gypsy moth. The ovipositing parasite prefers to attack moving cater-
pillars and tends to prod caterpillars to move, when the ovipositor is quickly
inserted and the egg deposited—the whole act taking just a second. The eggs
are usually deposited in the posterior part of the body cavity. Several eggs
may be deposited in one host but only one parasite matures.
Fecundity: The total number of eggs deposited by a female ranged between
182 to 1,228, in experiments of Muesebeck and Parker. The average number
was 061. The longevity of the ovipositing female varied between 12 days to
04 days. In most cases the female continued to oviposit until the last day of
her life, but the female that lived the longest deposited no egg after the 34th
day. Ona single day a female can deposit from 50 to 84 eggs.
Egg: The egg (Fig. 60) is 0.40 to 0.45 mm. in length and 0.11 to 0.14 mm.
in maximum width. It is slightly curved on one side, smooth and pearly white.
After deposition in the host, the egg gradually increases in size and before
hatching attains a length of 0.7 to 0.8 mm. anda width of 0.25 to 0.28 mm.
The duration of the egg stage is usually 7 days, which may extend up to 10
days when temperatures are low.
Larva: Five larval instars were distinguished by Muesebeck and Parker,
although in other related parasites only three have been observed by several
authors. Fig. 62 depicts larval mandibles.
The first larval instar is elongate more or less cylindrical, and smooth,
with a strongly sclerotized brown head, and a long caudal appendage, which is
72 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
a prolongation of the last, or thirteenth, body segment. On hatching, the
larva measures about 1.2 mm. in length, including the oval appendage, which
itself is 0.30 to 0.35 mm. long. The mandibles (fig. A) are small, but
heavily sclerotized and strongly hooked. The second larval instar is larger
in size, with less sharply defined head, differently shaped and less sclerotized
mandibles, and somewhat shorter caudal appendage. The larvae in the third
and fourth instars are generally similar to the second larval instar, but larger
in size and with differently shaped mandibles (fig. C, D). The fifth larval
instar has more heavily sclerotized mandibles, the labial ring and the sclerotic
framework in the mouth region are brown in color and conspicuous, body integu-
ment covered with minute tubercles, antennal leg and wing pads visible, and has
nine pairs of open spiracles. The first pair of spiracles is situated near the
posterior margin of the first thoracic segment, followed by a pair on each of
the first eight abdominal segments. The caudal appendage is greatly reduced,
resembling a short, thick, evenly tapering spine. The mature larva measures
8-10 mm.
The duration of each larval instar varies considerably, depending upon the
temperature. The following averages are reported by Muesebeck and Parker
after a large number of dissections:
I Instar . to 10 days
II Instar 2 to 5 days
III Instar 2 to 4 days
IV Instar 2 to 4 days
V Instar 1 to 2 days (within host)
The mature parasitic larva emerges from the fourth larval instar of the
gypsy moth host. The host is killed several hours before the mature parasitic
larva emerges. After emergence, practically nothing remains of the host
larva.
Cocoon: The mature larva spins a cocoon on the underside of leaves or
branches beside the dead host larva. The cocoon is ovoid in shape, measuring
6-7 mm. in length and 4 to 4.5 mm. in diameter (fig. 61), It is dark brown
in color with a broad grey band around its middle. An outer layer of compara-
tively loose silk covers the dense tough more or less parchment-like envelope.
The attachment of the cocoon to underside of leaf or host remains is rather
weak so that the cocoon drops to the ground within 48 hours of its formation.
Pupa: Twenty-four hours after cocoon formation, the short caudal appen-
dage retracts and becomes shrunken and dark in color. After four days within
the cocoon, the larva exhibits a slight constriction at the posterior margin of
the thoracic region and the developing eyes are weakly discernible. The me-
conium is usually cast about 6 days after the formation of the cocoon, and actu-
al pupation occurs on the 9th or 10th day. The pupa darkens gradually, until
at the end of about 5 days the head and thorax become black and the base of
abdominal petiole begins to darken. Transformation into a adult usually occurs
20-21 days after cocoon formation. The pupal stage thus covers 11 days.
The adult within the cocoon is fully formed during the first half of July,
although emergence does not occur until the following spring. There is thus
only one generation per year. Rarely a male may emerge in the same season
in which the cocoon was formed.
Muesebeck and Parker noted that the parasite dies within the cocoon if the
meconium dries out. Consequently it is important that the cocoons be stored
in sufficiently moist atmosphere to maintain the semiliquid condition of the
V. Gupta: Gypsy Moth Parasites 73
meconial discharge. Proper moisture conditions are important during ship-
ment of cocoons and during hibernation in the laboratory.
Duration of various developmental stages
Egg 7-10 days
Larva 12-25 days
Prepupa 9-10 days
Pupa 10-11 days
Adult 12-54 days
The total life cycle thus covers from 50 days to 110 days and is tempera-
ture dependent.
Hyperparasites
Several hyperparasites were reared from shipments received from Italy
during 1911 and 1912. These were:
Gelis areator (= Hemiteles areator Grav.).
Gelis sp. (3 unidentified species)
Theroscopus sp.
Spilocryptus pumilus Kriechbaumer
Bathythrix sp (= Thysiotorus sp.)
Theronia atalantae (Poda)
Itoplectis clavicornis (Thomson)
Itoplectis alternans (Gravenhorst)
Monodontomerus aereus Walker
Monodontomerus sp. |
Haltichella maculipennis De Stefani
Eurytoma appendigaster (Swederus)
2. PHOBOCAMPE LYMANTRIAE, new species (Figs. 52-56)
Male and female: Similar to P. unicincta in general sculpture and color,
and differing as follows:
Flagellum 26 to 28 (30) segments. Face somewhat rugulose. Malar space
shorter, 0.33+0.1 the basal width of mandible; in female usually 0.25 and in
male 0.35-0.4. Interocellar distance longer, 1.8+0.1 the ocellocular distance.
Ocellocular distance slightly less than the ocellar diameter. Propodeum granu-
lose, including petiolar area and areola, both of which are depressed and con-
cave and without striations. Sometimes a few striations seen at the junction of
areola and petiolar area only. Areola broadly open below costulae, not con-
stricted apically, with median longitudinal carinae weak in this area. Pro-
podeal carinae generally weaker. Basal transverse carina usually more
roundly arched medially. Areolet larger, more oblique, with a short petiole
and second recurrent vein at its outer corner. Nervulus usually distad of basal
vein by 0.25 its length. Discocubitus roundly arched, not very strongly so.
Postpetiole more abruptly widened from petiole. Junction between petiole and
postpetiole appears constricted. Lateral groove on petiole deeper and more
conspicuous than in unicincla, Postpetiole wider than long, its sides roundly
74 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
arched and margined by a distinct and sharp carina. Postpetiole widest at its
middle. Tergite 2 wider, less than 2.0 as long as its basal width; in male a
little narrower. Postpetiole finely granulose to mat, in males often granulose.
Epipleurum of tergite 4 with denser hairs, clustered along its apical margin.
Subgenital plate appears less hairy.
Black. Color similar to that of P. unicincta, but the black marks on hind
coxa, apex of hind femur and base of hind tibia usually faint, obsolescent or
even. Tergite 2 of female with a narrower yellow band, occupying its apical
0.25 only. Apex of tergite 1 hardly yellow. In males tergites 1 and 2 without
yellow or orange bands, often extreme apex of tergite 2 brown.
Variations: A few specimens from Madrid, Spain; Vees, Hungary; and
Bilky, Czechoslovakia; and a specimen each from Simantornya, Hungary; and
Bibai, Hokkaido, K. Kamijo, July 11, 1962; are like Phobocampe lymantriae
in the nature of malar space, interocellar distance, postpetiole and second
tergite, but the propodeum is more like that of P. unicincta in that the basal
transverse carina is angulate medially and areola and petiolar areas have
more carinations. The hind coxa also has faint to somewhat distinct black
apical marks. The malar space is rather small (0.2-0.25).
I believe these are P. lymantriae, as the areola is widely open behind, not
constricted and the longitudinal carinae are weak.
Length: 4-7 mm. Fore wing 3.5 to 5mm.
Holotype: ¢, SPAIN: Madrid, June 1925, ex Lymantria dispar, Gypsy
moth Lab. (FIS, Hamden, Ct.)
Allotype: ©: Same data as the holotype.
Paratypes: Spain: Same data as the holotype, 20°, 802, June-July 1925
(Hamden). Czechoslovakia: Bilky, 40, 8°, 1925, ex Lymantria dispar, Gypsy
Moth Lab., No. 3475 (Hamden). Hungary: Olaszliszka, 32, June 25, 1927,
ex Lymantria dispar (Hamden & Washington). Vees, Hungary, 1°, 19, July
12, 1928, and July 6, 1929, Gypsy Moth Lab., No. 13039 D and 13044 C
3 (Hamden). Debreczen, Hungary, Gypsy Moth Lab., 2°, No. 3469.
Jugoslavia: Moscenica, 1°, June 18, 1927, Gypsy Moth Lab., No. 13019 B
(Hamden). Vees, Hungary, 7%, 6¢, June 1928, ex gypsy moth (Washington).
Nieborow, Poland, 1%, 2°, May 1975, Fuester & Mura, emer. June 1975.
Skierniewice, Poland, 22, May-June 1975 Fuester & Drea. Burgenland,
Austria, 1°, April-June, 1974, Hoyer. South France, 20%, 3°, June 1972,
J. Drea (Washington & EPL, Paris). Foret d'Orleans (Loiret), France, 19,
May 1974 (EPL, Paris). Bouches du Rhone, France, 1%, June 1973, Fuester
and Gruber (Washington). Westwood, Mass., 22, June 1929, Gypsy moth lab.
No. 11532 (FIS, Hamden). Japan: Bibai, Hokkaido, 12, K. Kamijo, July 11,
1962, ex Lymantria dispar (Washington). Many specimens in Hamden collec-
tions were identified as ''Hyposoter species. "'
Cocoon: Cocoon slender, oblong, light brown in color, often with black
marks encircling the end opposite the exit hole and with a whitish silken central
band, 3x 6mm. or smaller, but about 2.0 as long as wide. Cocoons generally
smaller than those of P. unicincta.
Distribution: Europe (Spain, Czechoslovakia, Hungary, Yugoslavia,
Poland, Austria and France). China. Japan. ?U.S.A. (Introduced). It is
sympatric with P. unicincta over much of its range.
Biological notes: This species appears multivoltine, the adults emerge
in the same season in which the cocoons are formed. According to Dysart
(personal communication), Dr. Paul Schaefer also observed the multivoltine
nature in Phobocampe species collected in southern Japan from the gypsy moth.
The specimens examined from his collections, however, fit better with wnicincta
V. Gupta: Gypsy Moth Parasites 75
rather than with lymantriae.
The specimen collected by Kamijo in 1962 is the only Japanese specimen
fitting better under this species. The two specimens from Massachusetts,
collected as early as 1929 are interesting. There is no evidence whether they
were reared from the gypsy moth stocks in Europe or from Massachusetts.
Most specimens from Europe were mixed and it is likely that both these spe-
cies were released in the field. There is no evidence of its establishment in
the U.S.A.
A series of specimens from China: Heilongjiang Province reared from
Lymantria dispar in May-June 1982 by Schaefer ef al. have been examined.
They are Ph. lymantriae. A few have blackish hind femur, and propodeum a
little coarser. Three males and a female were also reared on Lymantria
mathura feeding on Salix. They also have darker hind femur.
6. Genus HYPOSOTER (Fig. 47)
Hyposoter Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 152.
For generic synonymy, refer to Townes, 1970: 181. Species of this genus
associated with the gypsy moth have often been referred to under the genus
Anilastus.
Moderately stout to slender species with fore wing 3.2 to 9 mm. long.
Eye margin weakly to strongly indented opposite antennal sockets. Malar
space 0.4 to 0.85 the basal width of mandible. Clypeus small, convex, its
apex also convex. Lower edge of mandible with a basal lamella that is rather
abruptly narrowed beyond the middle. Lower tooth of mandible a little smaller
than the upper tooth. Temple short to very short. Occipital carina joining
hypostomal carina. Thorax largely granulose to rugulose. Posterior meso-
sternal carina complete. Propodeal areola usually distinct and, in the species
treated here, closed behind. Petiolar area concave and its bounding carinae
often erased so that the combined petiolar area and third lateral area form a
shallow trough. Propodeal spiracle circular to short elliptic. Hind basitarsus
without a midventral row of closely spaced short hairs. Tarsal claws small,
pectinate. Areolet present, with second recurrent vein near apex. Nervulus
opposite basal vein or a little distad. Nervellus not intercepted, vertical to
weakly reclivous. Glymma present in the form of a deep pit. Abdomen com-
pressed apically. Thyridium circular or elliptic. Ovipositor short, 1.0 to
1.5 the apical depth of abdomen.
Members of the genus are parasitic within lepidopterous larvae.
Four species of Hyposoter have been mentioned in literature as parasitic on
Lymantria dispar: H. tricoloripes. (Viereck) in Europe, H. fugitivus (Say) in
North America, and H. vierecki T.M.&T. [=Campoplex (Diadegma) japonicus
Viereck] and H. takagii Matsumura in Japan. 4H. lymantriae (Cushman) occurs
in India on the related Lymantria obfuscata.
Campoplex vapax Gravenhorst, often referred to under the genera Anilastus
and Anilasia, appears to be a species of Hyposoter. It is unknown to me.
Anilastus n. sp. (Stadler, 1933) is alsoa Hyposoter, most probably H. tricolo-
ripes, judging from the figures of the larval remains.
"Hyposoter spp." of Burgess and Crossman (1929) represents Phobocampe
lLymantriae from Spain, and Central Europe.
Hyposoter fugitivus (Say) (= Limnerium sp =Limneria fugitiva) was wrongly
associated with the gypsy moth on guess-work. Its record in literature stems
76 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
from Howard and Fiske (1911: 138) who stated:
| ''A single cocoon, which was directly associated with the remains of the host
caterpillars [Lymantria dispar] was collected by Mr. R. L. Webster in 1906
during his association with the laboratory. It was very likely that of L. fugitiva
Say, but the fact will never be known, because a specimen of Hemiteles utilis
Norton, a hyperparasite, actually emerged. "'
KEY TO THE SPECIES OF HYPOSOTER FROM THE GYPSY MOTH
1. Larger-sized species, 8-11 mm. long. Propodeum largely rugose, with
basal areas somewhat rugoso-punctate. All coxae, trochanters and
femora black, the anterior ones may be brown. Abdominal tergites
marked with reddish-brown. Areola bounded by strong carinae. Japan,
Korres. an Chinas 6 eee el we Fo 1. takagii (Matsumura)
Smaller-sized species, about 6-7 mm. long. Propodeum largely granu-
lose. Petiolar area often rugose. Fore and middle trochanters yellow
to yellowish-brown. All femora yellowish-brown. Coxae black or
anterior ones yellow. Abdomen black. Areola bounded by weak to
moderately strong carinae. (In tricoloripes hind femur often brownish,
PAPOy Ole) ek ee a esd a ee er IA ae 2
2. Fore and middle coxae and trochanters yellow. Propodeum in basal and
lateral areas and inside areola granulose. Petiolar area granuloso-
rugulose. In male sculpture coarser, with petiolar area rugulose.
mlender species. Japane .oe . 6 Gs eo. 2. vierecki T.M.&T.
Fore and middle coxae black, as is hind coxa, or fore coxa partly yellowish-
brown. Slender to moderately robust in build. ... 9.2... 2 eee
3. Hind femur and tibia often brownish though at times lighter incolor. Areola
crescentic, about 2.0 as wide as long, its apical closing carina complete
and weakly arched. Propodeum largely granulose basolaterally. Pro-
podeal sculpture finer than in lymantriae. Scutellum finely granulose.
Second tergite granulose. Gastrocoeli usually deep and conspicuous.
BUPONG6s ss Oe WRIA eS Sraacieneaiy eA 3. tricoloripes (Viereck)
Hind femur reddish-brown. Hind tibia yellowish-brown with fuscous basal
and apical marks. Areola horse-shoe shaped, its apical closing carina
usually strongly concave, and carinae bounding areola often irregular or
incomplete. Propodeum in general coarser than in tricolorifes, with
lateral areas rugulose. Scutellum granuloso-punctate. Second tergite
mat to weakly granulose. Gastrocoeli shallow. India.
4. lymantriae Cushman
1. HYPOSOTER TAKAGII (Matsumura)
Casinaria takagit Matsumura, 1926. J. College Agr. Hokkaido Imp. Univ.,
18: 28. Korea. Host: Dendrolimus spectabilis.
Hyposoter takagii: Townes, Townes and Gupta, 1961. Mem. Amer. Ent.
Inst., 1: 242. China, Japan, Korea.
Hyposoter takagii: Yasumatsu and Watanabe, 1964. Catalogue of Insect
Natural Enemies of Injurious Insects in Japan, Pt. 1: 43. Hosts:
Lymantria dispar (cf. Fukaya, 1950), Dendrolimus spectabilis,
V. Gupta: Gypsy Moth Parasites 77
Malacosoma neustria testacea (cf. Hayashi, 1933).
This species has often been misidentified in Japan as Casinaria atrata
Morley (cf. Townes, Momoi and Townes, 1965: 300). It was first reported
from the gypsy moth by Fukaya (1950). It is distinguished from other Hyposoter
species by its larger size (8-11 mm.) and by the reddish marks on tergites.
Male and female: Face rugulose. Malar space 0.8 the basal width of man-
dible. Interocellar distance 1.7 to 1.8 the ocellocular distance. Vertex finely
granuloso-mat. Mesoscutum granuloso-rugulose. Scutellum rugose. Meso-
pleurum rugulose to finely rugose. Metapleurum rugulose. Propodeum largely
rugose, with basal areas somewhat rugoso-punctate to rugulose. Areola
bounded with strong carinae. Areola pentagonal or hexagonal with its apical
closing carina assuming various shapes—straight, arched, or angled. Median
longitudinal carinae separating petiolar area from third lateral area weak to
distinct and convergent apically. Postpetiole shiny or finely mat. Second
and the following tergites mat to subpolished. Thyridium larger, wide,
separated from base of second tergite by about half its width.
Black. Mandible partly to wholly, palpi, tegula partly (or not so), and
fore and middle tibiae and tarsi, yellow. All coxae, trochanters and femora
black to blackish-brown, particularly the anterior ones. Hind tibia and tarsus
brown to blackish-brown. Abdomen black with some tergites often marked with
reddish-brown. Abdomen never appearing wholly black. Color of legs and
abdomen variable, with more or less of reddish color.
Specimens: Several males and females from Japan, China, and Korea
examined, reared from Dendrolimus spectabilis and Malacosoma neustria.
No specimen from the gypsy moth available.
Distribution: China, Japan and Korea.
2. HYPOSOTER VIERECKI T.M.&T.
Campoplex (Diadegma) japonicus Viereck, 1912. Proc. U. S. Natl. Mus.,
42: 636. Name preoccupied by Cameron, 1906. Japan. "Gypsy Moth
Lab. No. 1071".
Hyposoter viereckit Townes, Momoi & Townes, 1965. Mem. Amer. Ent.
Inst., 5: 302. New name.
This species is readily distinguished from the others treated here by its
yellowish-white fore and middle coxae and trochanters and yellowish-brown
femora.
Male and female: Face and clypeus granulose. Malar space 0.65 the basal
width of mandible. Interocellar distance 2.0 the ocellocular distance. Frons
and vertex finely granulose. Thorax granulose. Pronotum and mesopleurum
with a few striations interposed amongst granulations. Sculpture of scutellum
a little coarser. Propodeum largely granulose. Combined petiolar and third
lateral area ruguloso-granulose. Areola rectangular to squarish, its
bounding carinae sharp to weak, apical closing carina angled medially. Areola
rugulose to granulose. Costula incomplete. Sculpture of male propodeum
coarser, particularly within areola and in petiolar area. Postpetiole and
second tergite finely granulose. Other tergites progressively mat to sub-
polished. Thyridium rather small and narrow, separated from base or second
tergite by about its width.
Black. Mandible, tegula and fore and middle coxae and trochanters, light
yellow. Fore and middle legs otherwise yellowish-brown. Hind coxa black,
78 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
trochanters blackish, trochantellus in female yellowish-brown, femur brownish-
yellow, tibia yellowish-brown with fuscous marks apically, and tarsus fuscous.
Sometimes apex of hind femur and base of hind tibia also fuscous.
Length 6-7.5 mm. Fore wing 4-5.5 mm.
Specimens: Japan: 1° (type, No. 7258 of Campoplex japonicus Viereck),
"Gypsy Moth Lab. No. 1071, June 21" (Washington). Japan: Kamifurano,
Hokkaido, 1%, 19, July 1, 1975, P. Schaefer, ex Lymantria dispar (Washing-
ton); 2°, June-July 1975 (BIRL, Newark). Hobetsu, Hokkaido, 1% (broken),
June 15, 1978, emerged June 25, 78, P. Schaefer (BIRL, Delaware). 1 ex
(without abdomen), "Asagawa"', June 16, 1923 (Washington).
According to Carlson (1979: 661) some of the records Phobocampe unicincta
in Japan may pertain instead to the present species.
3. HYPOSOTER TRICOLORIPES (Viereck) (Figs. 63-67)
Anilastus tricoloripes Viereck, 1911. Proc. U. S. Natl. Mus., 40: 478.
Europe. "'Gypsy Moth Lab. Nos. 1079 and 1065"'. Type is a female,
not a male (no. 1079). Paratype is a male (no. 1065).
Limnerium (Anilastus) tricoloripes: Howard and Fiske, 1911, U. S. Dept.
Agr. Bur. Ent. Bull., 91: 192.
This species has often been reared in Europe at different places from the
sypsy moth and imported into the U.S.A. for release. In 1911, Howard and
Fiske reported, ''From time to time several specimens of Limnerium cocoons,
all of them oblong in shape, and most of them partly concealed by the skin of
the host caterpillar, have been received from Europe. In no instance they have
been in sufficiently large numbers to make the species appear promising as a
parasite. "
Pschorn-Walcher (1974) reported it to be a larval parasite of low incidence
in southern France, eastern Austria and Bavaria.
Male and female: Head granulose. Face a little coarser in male. Temple
and occiput subpolished. Malar space 0.9 to 0.6 the basal width of mandible.
Ocelli comparatively large, so that they appear somewhat closer to eye.
Interocellar distance 2.2 to 2.3 the ocellocular distance. Mesoscutum,
scutellum and mesopleurum granulose, almost of the same intensity. Speculum
distinctly granulose, dull. Metapleurum a little finely granulose. Propodeum
eranulose. Petiolar area granuloso-rugose or rugulose in female and rugose in
male. Areola granulose, crescentic, bounded by sharp carinae, about 2.0 as
wide as long, closed apically. Costula complete to incomplete. Postpetiole
and second tergite granulose. Rest of abdomen granuloso-mat to mat apically.
Gastrocoeli deeply impressed, oval to crescentic, separated from base of
second tergite by 0.5-0.7 its width. Ovipositor sheath appears a little widened
apically. Ovipositor a little shorter than apical depth of abdomen.
Black. Mandible, palpi, tegula, and fore and middle trochanters, yellow.
Fore and middle femora yellowish-brown to reddish-brown, their tibia and tarsi
yellowish and with fuscous marks. All coxae black. Fore coxa sometimes
apically brownish or yellow. Hind leg brownish, though at times lighter in
color, or seldom hind femur blackish. Apex of tibia often darker, or hind
tibia brown with its base pale yellow.
Length: 5.5-7.5 mm. Fore wing 4-5 mm.
Specimens: Europe: Type ¢ and paratype %, ''Gypsy moth Lab., Nos.
1079 and 1065", Type No. 13799 (Washington). Europe: Several males and
V. Gupta: Gypsy Moth Parasites 79
females reared from the gypsy moth at Oberpullendorf, Austria, June 18,
1931; Austria, July 1932; Burgenland, Austria, May-July 1974; Orleans,
France, June 1972 and May 1976; Neuf Brisach, France, May 1976; France,
June 1980; and Nieborow, Poland, June 1975 (Hamden, Washington and Paris).
The specimens in Hamden were identified as Hyposoter sp.
Distribution: Europe. The female type is rather abnormal. It is a small
Specimen with a very different areola—which is rather oblong and open
apically. Viereck (1911) noticed this difference between the type and the para-
type. I believe that the areola is rather abnormal in the type-specimen, as
this condition is not seen in other specimens reared from the gypsy moth.
It appears that this species has been released in the U.S.A. in recent
years but the results have not been encouraging. Drea and Fuester (1979)
observed, ‘Information on the biology of H. tricoloripes indicates that an
alternative host is probably required for the species to complete its annual
cycle. This may be the reason why this parasite has never become estab-
lished in North America despite repeated releases.
4. HYPOSOTER LYMANTRIAE Cushman
Hyposoter lymantriae Cushman, 1927. Rec. Indian Mus., 29: 244. India:
Kangra in Himachel Pradesh. Host: Lymantria concolor.
Hyposoter lymantriae: Beeson and Chatterjee, 1935. Indian Forest Rec.
(N.S.) Ent, , 1: 161. biol:
This species occurs in Northern India on Lymantria obfuscata and Lyman-
tria concolor, which are related to the gypsy moth. It is rather close to the
European tricoloripes, but is coarser in sculpture, with areola differently
shaped and malar space and interocellar ratios a little different. The hind leg
color is lighter. ,
Male and female: Head granulose. Temple and occiput subpolished. Malar
space 0.75 the basal width of mandible. Ocelli comparatively small, appearing
farther from the eye than in tricoloripes. Interocellar distance 1.8 to 2.0 the
ocellocular distance. Mesoscutum granulose. Scutellum and mesopleurum
granuloso-punctate. Speculum a little more convex and subpolished than in tvi-
coloripes and finely weakly striate. Metapleurum and pleural area of pro-
podeum weakly granulose, subpolished. Propodeum granulose on front half.
Areola granulose to rugulose, more arched in front, its lateral carina and
apical closing carina often weak or incomplete. Costula usually distinct and
complete. Areola often irregular in outline. Second lateral area rugulose.
Combined petiolar and third lateral area rugose. Postpetiole finely granulose.
Second tergite mat to weakly granulose, and the following tergites mat to sub-
polished. Ovipositor sheaths appear slender. Ovipositor equal to apical depth
of abdomen.
Black. Mandible, palpi, tegula, and fore and middle trochanters, yellow.
Fore and middle femora yellowish-brown, their tibiae and tarsi yellow with
pale brown marks. Hind femur reddish-brown, tibia yellowish-brown with apical
and subbasal fuscous marks or bands. Hind tarsus brownish to blackish, with a
pale basal band on first segment. Coxae black with fore coxae often yellow
apically.
Length: 6-7mm. Fore wing 4.5-5 mm,
Specimens: India: Kulu in Himachal Pradesh, 2, 22, and 2 broken sp.,
June 1964, ex larva of Lymantria [obfuscata} (Gupta). Kulu Dist.: Katrain,
80 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
ex larva of Lymantria |[obfuscata], 1° (CIBC, Bangalore) and 12 (Washington).
Katrain, Kulu, 1%, June 26, 1965; Shambi, Kulu, 1°, May 19, 1965, ex
Lymantria |obfuscata] on Alnus nitida, and determined as Anilastus sp. (CIBC,
Bangalore). Srinagar, 1%, June 1969, ex Lymantria obfuscata, det. as
Hyposoter sp. (CIBC, Bangalore). India: Kangra Forest, August 15, 1917,
O. H. Walters Coll., 19% (type of H. lymantriae), parasite of Lymantria
concolor (Washington).
Beeson and Chatterjee (1935) gave the following biological information:
"Host: Lymantria concolor Walk. (Lymantriidae) defoliating Quercus incana."
"The host is attacked in the early larval instars during June-July; the parasite
matures in August and the host in September-October. "'
Dr. Roger Fuester (BIRL, Delaware) recently sent me specimens of this
species, which were reared at Newark on the gypsy moth from stocks from
Kulu District, India. It is intended to be released in the Northeastern U.S.A.
against the gypsy moth.
il.. SUBFAMILY ICHNEUMONINAE
Members of the subfamily Ichneumoninae are characterized by having the
clypeus relatively flat, separated from the face by a weak groove, its apical
margin weakly arcuate, or truncate, with or without a blunt median point.
Upper tooth generally longer than the lower, notauli and sternaulus absent, or
short and shallow, except rarely, propodeum steeply sloping in the petiolar
area, with longitudinal carinae, areola present, variously shaped and often
raised, propodeal spiracles linear (circular in some tribes that are not treated
here), areolet pentagonal, the intercubiti convergent towards radius, abdomen
flattened, usually spindle-shaped, first segment quadrate basally in cross
section, with its spiracles placed far beyond the middle, postpetiole flattened
and wide or pyramidally raised, gastrocoeli usually wide and distinctly
impressed, and ovipositor generally short, hardly surpassing the tip of the
abdomen. The female flagellum is usually widened preapically and the male
flagellum is slender and tapering.
The species of Ichneumoninae are internal parasites of a variety of lepi-
dopterous pupae. The oviposition is usually in the pupa but sometimes into the
larva and the emergence from the pupa.
Several species of Ichneumoninae have been listed as parasites of the gypsy
moth, chiefly in Europe. Most of them, however, have never been recorded
subsequently and reared specimens are not available to confirm their occurrence
on the gypsy moth. The only exception is Lymantrichneumon disparis (Poda),
which was perhaps the first ichneumonid recorded from the gypsy moth and
which has been collected subsequently in small numbers from the pupae of the
gypsy moth.
There are some /apsi in the literature regarding the association of the
ichneumonine species with the gypsy moth. Rudow (1911) listed several
Species as parasites of both Lymantria monacha and L. dispar, viz., Ichneu-
mon raptorius, I, sugillatorius, I. melanoceras, I. fabricator, and Trogus
flavatorius. In his subsequent lists (1917-1919) he was more specific as to the
host records. In 1918, Ichneumon vaptorius, sugillatorius, and melanoceras
were listed as parasites of Lymantria monacha and not of dispar, while I.
fabricator was not mentioned from either of them. These species are omitted
here, except I. fabricator, which has been subsequently recorded as a gypsy
moth parasite by Cecconi (1924) and Gyorfi (1963) and Trogus flavatorius, which
V. Gupta: Gypsy Moth Parasites 81
is the same as Lymantrichneumon disparis, There are a few other species,
apparently first reported by Rudow (1917-19) from the gypsy moth, but missed
by Schedl (1936) and Thompson (1946). These are included, although, as is
usually the case, subsequent rearing records are lacking.
The identification of the genera and the species of the Ichneumoninae is
somewhat difficult. In the keys that follow, attempts have been made to
simplify them and a field key based largely on color is also given. For more
information on the taxonomy of genera and species, the following works may
be consulted: Heinrich (1960-62), Perkins (1953, 1959-60), Townes, Momoi
and Townes (1965), and Kasparyan (1981).
KEY TO THE ICHNEUMONINAE ASSOCIATED WITH THE GYPSY MOTH,
INCLUDING A FEW RELATED GENERA
1. Petiole wider than deep, flat above. Clypeus projecting forward, triangu-
lar in outline. Mandible strong, with one tooth. Body black, femora
yellow. (Tribe Pristocerotini).......... 13. Cotiheresiarches
[ Cotiheresiarches dirus (Wesmael)]
Petiole as deep as wide, Squarish in cross-section. Otherwise not as
2. Clypeus wide, its apical margin thin and convex. Face and clypeus in an
even plane. Temple strongly widened behind eye. Occipital carina
reaching hind corner of mandible, not joining hypostomal carina. Man-
dible wide, not or very little tapered apically, both teeth prominent.
CT YUAe: GeOne TA ie 4s. Gate BN WEE OGL 2 LR REL 3
Clypeus narrower, its apical margin thicker and usually arcuate or
truncate. Clypeus and face not forming a flat surface. Either clypeus
and face with median convexities or their junction depressed. Temple
moderately swollen. Occipital carina joining hypostomal carina.
Mandible moderately narrow and tapered apically, with lower tooth
CLOT SURG GE BU ig on hs ee Ae AT laa SR eee mee ae 4
3. Tarsal claws not pectinate. Metapleurum separated from propodeum by a
carina. (Recorded from Lymantria sp. and L. monacha. .. Geodartia
(G. cyanea: Large size, 22 mm. Abdomen apically compressed,
obtuse at apex and metallic bluish.
Tarsal claws pectinate to apex. Metapleurum separated from propodeum
PY EAL EO Ra a in sien aencedel a wrhe ct mehr ad PW ROO de Pseudomaraces
(P. melli Heinrich reported from Lymantria sp.)
4. Propodeum convex on front half or less (up to areola). Propodeum in
profile view raised basally and then abruptly sloping. Areola usually
constricted, horse-shoe shaped, or in the form of a raised polished
"boss", its bounding carinae often flat and polished. Incisures between
tergites usually deep. Tribe Ichneumonini (Protichneumonini). ... 5
Propodeum flat on basal half and then sloping. In profile view propodeum
making an inclined slope. Areola normally formed, squarish or elongate,
or sometimes arched basally. Tribe Joppini. ............
5. Areola reduced to a small polished boss that is strongly elevated, its
bounding carinae obsolete. Apex of female abdomen blunt (amblypygous).
82
10.
a1.
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Gastrocoeli shallow.and Wide. io... .i6 see es “a cue 3.2 Callajoppa
[Callajoppa cirrogaster cirrogaster (Schrank)].
Areola normal or somewhat normal, bounded by distinct carinae. Apex of
female abdomen acute (oxypygous). Gastrocoeli usually deep. .... 6
Abdomen black or bluish-black, with or without white spots, spindle-shaped,
a little narrower than thorax. Areola within the general convex surface
of propodeum, not distinctly raised, usually horse-shoe shaped or
NORA CORAL 6 i ee ee OO Ale eae SG 4. Ichneumon
(Several species).
Abdomen more parallel-sided, reddish or brownish, as wide as thorax.
Areola raised above the general surface of propodeum, propodeum
sloped away from areola on all sides. Pyrotichneumon and related
Scutellum flat, polished. Areola rugose, longer than wide. Postpetiole
not pyramidally raised. Head and thorax black. Abdomen reddish.
Wines clear hyaline. cols ao ee Ss 2. Paracoelichneumon
[Paracoelichneumon rubens (Fonscolombe)].
Scutellum subconvex, punctate. Areola horse-shoe shaped, smooth.
Postpetiole somewhat pyramidally raised medially. Body yellowish-
brown with wings yellow tinged. ......... 1. Lymantrichneumon
[Lymantrichneumon disparis (Poda)].
Thyridia very wide, the space between them less than 0.7 the width of
CAC ee a rs a 9
Thyridia of moderate width or narrower, the space between them more
than 0.7 the width of each. Thyridia usually weakly impressed. .. 10
Lateral carina of scutellum sharp and strong up to apex of scutellum.
Postpetiole granulose to punctate, usually without a defined median
DOL ea a ee Ge ee ea eee an Do. stenaoplus
[Stenaoplus pictus (Gravenhorst)].
Lateral carina of scutellum ending at basal 0.2 to 0.3. Postpetiole with a
distinct median field, which is striate. ......... Stenichneumon
(not associated with the gypsy moth).
Extreme base of propodeum with a weak median tubercle. Median field of
postpetiole with moderately dense punctures. Apical half of female
flagellum strongly flattened below, tapering apically.
6. Melanichneumon
[Melanichneumon leucocheilus (Wesmael)].
Base of propodeum without any median tubercle. Median part of postpetiole
with fine to distinct longitudinal striations or aciculations. Apical half of
female flagellum cylindric, blunt or tapering apically. ........ 11
Median field of postpetiole not sharply demarcated, with fine weak striations
and punctures. Apical half of female flagellum cylindric or weakly
Pisttened DelOwWe: soec8 i Rs Ga CO eae 7. Cratichneumon
[Cratichneumon fabricator (Fabricius)].
Median field of postpetiole demarcated and usually aciculate or strongly
striate. Apical half of female flagellum with a short to long taper, or
somewhat blunt apically (In Spilichneumon occisor, postpetiole finely
12.
13.
14.
15.
16.
17.
V. Gupta: Gypsy Moth Parasites 83
striate with smoother apex, and median field rather weakly demarcated).
Scuisiiagiy YErow. 67 ee ae ee re ee 12
Tip of abdomen acutely pointed (oxypygous). Ovipositor not unusually
short, distinctly exerted beyond abdominal tip. Subgenital plate not
elongate. Sternite 4 membranous medially (usually medially folded).
13
Tip of abdomen rounded (amblypygous). Ovipositor unusually short,
hardly exserted. Subgenital plate sometimes with a median prolongation.
Sternite 4 often not membranous medially. .........2..s+se-6 14
Apical margin of clypeus broadly, weakly concave, with a weak, broad,
median tooth. Apical part of female flagellum blunt, not distinctly
tapered betore the last sezsment. se ee: 8. Chasmias
[Chasmias paludator (Desvignes)].
Apical margin of clypeus truncate or weakly convex, without a median
tooth. Apical part of female flagellum weakly tapered.
9. Pterocormus
[Pterocormus sarcitorius sarcitorius (Linnaeus)]. hice Sates
Flagellum short, its second segment 0.8 to 1.4 as long as wide, its apex
with a short taper. Sternite 4 not membranous medially. ...... 15
Flagellum long, slender, its second segment 1.4 to 3.0 as long as wide,
its apex with a long taper. Sternite 4 often membranous medially. . 16
Areola about 1.0 as long as wide. Sides of median field of postpetiole
BURLY GGG aie ee ye gee ae ees 10. Triptognathus
[Triptognathus amatorius (Mueller)].
Areola about 1.8 as long as wide. Side of median field of postpetiole
locistincty adelined. re Oe ee ee 11. Spilichneumon
[Spilichneumon occisor (Fabric re:
Subgenital plate with a median apical tuft of suberect hairs. Eutanyacra
[Not associated with the gypsy moth].
Subgenital plate without a median apical tuft of hairs, often with a few
longer hairs on its apex but these sparse and either decumbent or only
WRT POV cg et ene GRE ee RM Be kee 17
Propodeum with an acute tooth at apex of its second lateral area on either
Oe he 8 we ee ge oe Gre 12. Amblyteles
|Amblyteles armatorius (Foerster)].
Fropoaeum witout eet, sen Ee See iy ee Se aa Diphyus
FIELD KEY FOR THE IDENTIFICATION OF ICHNEUMONINE PARASITES
ie
ASSOCIATED WITH THE GYPSY MOTH
Body wholly black. Legs may have yellow or brown marks. Wings clear
HYeTne' Or A Tate iniecate rd eco arnt mia ane vatmrnrer ry eee nT 2
Body wholly to largely rufous brown, or black with abdomen striped, or
thorax black and abdomen reddish or rufous. ............. 8
84
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Sigeclaree,. 7190 10. FS. 1Onee 4s ee seo ies Bide ewer ee GS 3
Sime GMiG]t to Ri OP TESR Cope Fe eS ee wl ile 7
Fore and middle legs rufous. Scutellum black. ..........0... 4
All legs black. Scutellum yellow (or black in dirus)........... 5
Antenna black. Wings infuscate (according to original description). Hind
leg wholly black. Not seen. ... %, 2. "'Amblyteles varipes Rudow."'
Antenna brownish-black. Wings clear hyaline. Hind femur and tibia
DOONIGH. § a a kueia ees Oo, Chasmias paludator (Desvignes)
Abdomen with white spots on tergites 2-3 in? and 2-4 in@. Areola flat.
Oo, 2. Ichneumon cyaniventris Wesmael
(Ichneumon sugillatorius, ex Lymantria monacha, very much like the above
but the areola more convex).
Abdomen wholly black, without spots. Areola convex, a little raised. . 6
All femora yellowish-brown. Clypeal margin triangular, its apex project-
ing forward. Abdomen robust. Petiole flat above. Scutellum black,
RONVGR See: Ss eae & Raw ek °. Cotiheresiarches dirus Wesmael
All femora black. Legs wholly black, except in males where fore and
middle legs with brownish patches. Clypeal margin truncate or arcuate,
its apex not projecting forward. Abdomen spindle-shaped, slender.
Petiole quadrate in cross section. Scutellum yellow and flat.
o, . Ichneumon leucocerus Gravenhorst
(Incorrect record. Occurrence on the gypsy moth not confirmed).
Face strongly punctate. Body conspicuously marked with red and yellow.
Inner orbits yellow. Scutellum yellow at apex. All femora reddish.
Hind tibia without a yellow median band. Size 6-10 mm.
co, Stenaoplus pictus (Gravenhorst)
Face with scattered punctures. Body largely black, not conspicuously
marked. Face wholly black (9), or largely yellow (“). Scutellum black
(F) or apically yellow (%). All femora reddish (¢) with tibiae yellow
medially, or hind leg wholly brownish-black (“). Size 8-11 mm.
o, ¢. Cratichneumon fabricator (Fabricius)
Body largely to wholly rufous-brown. Thorax may have black patches.
POGOmInA Tin may be UAC kk or a ek he eke 9
Body black with abdomen banded or wholly reddish. Thorax black. Head
Pe Oly VOLO ks Wei iieck oe aoe) dca ha vem ce a ee BU 10
Head, thorax, abdomen, and legs largely rufous brown. Abdomen black
tipped. Gastrocoeli deep and wide. Postpetiole coarsely striato-
punctate. Wings yellowish-brown. Size 17 mm. or more, large.
o, 2. Lymantrichneumon disparis (Poda)
(Some Japanese specimens have less or more extensive black marks on
thorax, abdomen and legs).
Head blackish, except for face. Propodeum blackish. Rest of body
including tip of abdomen rufous. Gastrocoeli shallow. Postpetiole
granulose. Size small, 7-10 mm. . ?. Stenaoplus pictus (Gravenhorst)
10.
it:
12.
13.
14.
15.
16.
Lis
V. Gupta: Gypsy Moth Parasites 85
Thorax black. Head wholly black or dorsally black. Abdomen reddish or
yellowish-brown, with or without black on its apex. Abdominal tergites
not banded. Wings tinged or clear hyaline. ........2-+-e-+eee-e 11
Thorax black. Head black. Abdomen banded (yellow and black, or red
and black). Wings clear hyaline... 2... 61 eee ee eee ee ee 15
Size large, 20 mm. and over. Abdomen yellowish-brown, with apex black.
Wings lightly to strongly yellow-tinged. Flagellum not banded. Scutel-
lum subconvex to pyramidal. Areola quadrate or in the form of a polished
DOs. O45, SBP ae OE er ON ee ee eee ee 12
Size medium, less than 20 mm. long. Wings clear hyaline or a little
tinged. Abdomen reddish. Flagellum with a white band in’. Areola
elongate and rugose. Scutellum flat... . 1... ee ee eee eee 13
Scutellum pyramidal. Areola in the form of an elevated polished boss.
Wings strongly tinged with yellow. Basal four tergites yellow.
o, 2. Callajoppa cirrogaster cirrogaster (Schrank)
Scutellum subconvex. Areola quadrate, well formed. Wings lightly tinged
with yellow. Basal segment of abdomen and fourth and the following
segments black, only 2-3 segments yellow.
Oo, Triptognathus amatorius (Mueller)
Tip of abdomen white marked. Abdominal tergites 2-4 reddish (2) or with
reddish bands (“). Gastrocoeli and thyridia weak, indistinct.
o, 2. Melanichneumon leucocheilus (Wesmael)
Tip of abdomen black or red. Scutellum yellow. Areola elongate and
Abdomen beyond tergite 3 black. Tergite 7 may have a longitudinal
yellowish mark. Gastrocoeli weak and short. 4th sternite membranous
medially. Tip of flagellum blunt. Propodeum flat basally. Size 14-15
rans ae eal ee eT 7 eG 2. Chasmias paludator (Desvignes)
Abdomen red except for tergite 1. Gastrocoeli deep and wide. 4th ster-
nite wholly sclerotized. Flagellar tip pointed. Propodeum convex
DAES OIE EP RS @. Paracoelichneumon rubens (Fonscolombe)
Females. Flagellum with or without a white band............ 16
Mates. Flagellum without'a white band. eae re ee es 19
Second tergite black, only narrowly yellow basally. (Abdominal tergites
black with yellow bands). Propodeum with a sublateral acute tooth on
either side. Flagellum slender, finely tapered, without a white band.
. Amblyteles armatorius (Forster)
Second tergite red. Propodeum without sublateral teeth. Flagellum short,
curled apically and short tapered, with an indistinct white band... 17
Third tergite also red. Tergites 4-6 with median apical yellow incomplete
bands. Median field of postpetiole less strongly demarcated and finely
striate. Mandible not narrowed apically. Flagellum narrowed apically.
9. Spilichneumon occisor (Fabricius)
Third tergite largely black, with yellow apical margin or red with base
broadly black. Median field of postpetiole clearly defined and distinctly
striate. Mandible slightly to strongly narrowed apically. ...... 18
86 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
18. Third and the following tergites black with narrow apical yellow stripes.
Abdominal tip amblypygous. Tip of flagellum tapered apically. Femora
black. 6. eo ?. Triptognathus amatorius (Mueller)
Third tergite black in basal 0. 4 and red in apical 0.6. Tergites 4, 5, and 7
wholly black. Tergite 6 largely yellow. Abdomen oxypygous. Flagellum
rather blunt apically. Short tapered. Femora red.
Pterocormus sarcitorius sarcitorius (Linnaeus)
19. Second tergite yellow on basal half or more. Third tergite wholly to
largely yellow. Hind femur largely to wholly black. Face without a
DiAC i INA cee eiGs a we 6 ses ee we OS Aes Ee ee 20
Second and third tergites largely black, with yellow apical concave stripes.
(Abdomen banded by yellow and black). Face with a black mark. Hind
femur yellow on basal 0.75.
o, Pterocormus sarcitorius sarcitorius (Linnaeus)
20. Propodeum with a sharp tooth on either side. Flagellum brown. Hind
femur yellow on basal 0.25, otherwise black. Tergites 4-9 black.
o&, Amblyteles armatorius (Forster)
Propodeum without teeth. Flagellum black. Hind femur wholly black.
Tergites 4-5 with yellow apical bands.
Oo, Spilichneumon occisor (Fabricius)
TRIBE ICHNEUMONINI (= PROTICHNEUMONINI)
1. Genus LYMANTRICHNEUMON
Lymantrichneumon Heinrich, 1968. Ent. Tidskr., 89(1-2): 104.
Mandible apically narrowed and twisted so that the small lower tooth lies
behind the long and pointed upper tooth. Flagellum of female a little widened
subapically. Scutellum convex, raised from metascutellum and punctate. Its
lateral carina confined in its basal 0.3. Mesopleurum coarsely punctate.
Mesepisternum without a knob-like protuberance near middle coxa at its junc-
tion with mesosternum, so that in profile view this area does not appear con-
cave (cf. Protichneumon). Propodeum with a horse-shoe shaped high areola.
Petiolar area concave and abruptly sloping. Postpetiole wide, knob-like.
Gastrocoeli deep and wide, the interspace between them about 0.7 as long as
the width of gastrocoeli. Abdomen punctate and acute apically in the female
(oxypygous).
Color yellowish-brown with wings tinged with yellow. The Japanese speci-
mens often with black parts.
Heinrich (1968) segregated Lymantrichneumon from Protichneumon for the
reception of those species which are parasitic upon Lymantriidae rather than
Sphingidae. He distinguished Lymantrichneumon from Protichneumon by the
absence of a raised knob-like projection on mesepisternum near middle coxa
in the region of sternaulus, which is angled broadly with mesosternum, convex
propodeum at a level higher than that of metascutellum, apical margin of meso-
sternum not concave and raised, and mesoscutum densely punctate. He further
separated it on its body color: yellowish to orange brown with yellow-tinged
wings.
Heinrich (1960) stated that the females of the tribe Protichneumonini do not
V. Gupta: Gypsy Moth Parasites 87
hibernate as adults and probably produce only one generation per year, while
the adult of Lymantrichneumon does hibernate.
1. LYMANTRICHNEUMON DISPARIS (Poda)
Sphex disparis Poda, 1761. Insecta Musei Graecensis, p. 107, no. 3.
Europe. Host: Lymantria dispar.
Protichneumon disparis: Morley, 1903. Ichneumonologia Britannica,
1: 20. :
Ichneumon disparis: Howard and Fiske, 1911. U.S. Dept. Agr. Bur. Ent.
Bull., 91: 85, 239. ''Reared in Lab.".
Lymantrichneumon disparis: Heinrich, 1968. Ent. Tidskr., 89: 104-105.
Europe.
This species was the first ichneumonid parasite described from the gypsy
moth. It has been reared several times in Europe and there are several syn-
onyms of it, which are given by Dalla Torre (1901-02) and Uchida (1941). Those
synonyms that have appeared in the gypsy moth literature are: Ichneumon
flavatorius Fabricius, Tvogus flavatorius Panzer, Ichneumon ventralis
Matsumura, Protichneumon disparis orientalis Heinrich, Protichneumon dis-
paris matsumurai Uchida, and P. disparis segmentalia Uchida. This species
has also been put under various genera, like Amblyteles, Ichneumon, Coel-
ichneumon, Protichneumon, and lately under Lymantrichneumon.
Face with scattered punctures, extending to base of clypeus. Clypeus
smooth and shiny on apical half, with only a few sparse punctures. In female
central area of face more densely punctate. Apical margin of clypeus weakly
indented medially. Mandible apically tapering, its lower tooth small, less
than half.as long as the upper tooth. Vertex, upper areas of frons and upper
temples with shallow scattered punctures. Antennal scrobes smooth and shiny,
frons just in front of median ocelli trans-striate. Area between lateral ocelli
and occipital carina closely irregularly punctate. Ocellocular space granulose
and a little longer (10: 9) than the interocellar space, which is smoother.
Ocelli in male a little raised. Temple wide medially, a little wider than the
diameter of eye in side view. Mesoscutum closely ruguloso-punctate. Scutel-
lum subconvex, punctate, carinate laterally only at base, the carina blunt.
Apex of scutellum elevated from metascutellum and not in the same plane.
Metascutellum subpolished, with a few scattered punctures. Mesopleurum and
metapleurum with larger punctures, which are often aciculate at places, parti-
cularly infemale. Propodeum rugose, areola and basal area subpolished.
Areola semicircular or oval, with its apical closing carina arched inwards.
Petiolar area concave and abruptly sloping from areola. Median longitudinal
carinae bounding petiolar area more or less parallel-sided. Lateral longitu-
dinal carina indistinct so that second lateral area and second pleural area con-
fluent. Spiracular area not separated from second pleural area. Postpetiole
flat, widened, its median area raised, like a low pyramid, and striato-punctate.
Its sides with irregularly coalescent punctures. Abdomen longitudinally
striato-punctate. Gastrocoeli deep and wide, space between them less than
their width (0.7) and aciculate. Abdomen of female acute at apex.
Yellowish-brown. Orbits yellow. Flagellum dark brown basally and black
apically. Tip of abdomen (tergites 5 and beyond) black. Wings pale yellowish-
brown.
Variations: Body often narrow with blackish marks on mesoscutum, meso-
88 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
pleurum, metapleurum, apex of propodeum, and hind femur. In the Japanese
forms described as segmentalia, the thorax is more extensively black and in
the form matsumurai, the thorax, abdomen, hind femur and hind coxa are
largely black.
Length: 15-17mm. Fore wing 11-12 mm.
Specimens: Several males and females reared from the gypsy moth seen
from Italy, Hungary, and Austria.
Distribution: Europe.
Hosts: Lymantria dispar, L. monacha, L. dissoluta, Leucoma salicis,
Orgyia antiqua, Mimas tiliae, and Smerinthus ocellatas.
2. Genus PARACOELICHNEUMON
Paracoelichneumon Heinrich, 1978. Eastern Palaearctic Ichneumoninae
(in Russian). Acad. Sci. USSR., p. 13.
Mandible narrowed apically, but not twisted so that both the teeth are in the
same plane. Lower tooth blunt and short. Scutellum flat, in line with meta-
scutellum, shiny and with scattered punctures. Mesopleurum with well formed,
often evenly spaced punctures, not coarsely punctate. Areola elongate, rugose,
extending up to basal 0.3 of propodeum. Petiolar area abruptly sloping, not
concave. Mesoepisternum without a knob-like elevation near hind coxa and in
profile view not appearing concave at its margin with mesosternum (cf. Pro-
tichneumon). Gastrocoeli deep and wide, space between them less than 0.7
their width, and rugoso-striate. Postpetiole rugose. Abdomen closely punc-
tate, in female acute apically.
Paracoelichneumon is rather close to Lymantrichneumon and is distinguished
by its flat and more polished scutellum, areola, rugose, postpetiole not pyra-
midally raised, and by its clear hyaline wings. The body is black with the legs
and abdomen reddish.
1. PARACOELICHNEUMON RUBENS (Fonscolombe)
Ichneumon rubens Fonscolombe, 1847. Ann. Soc. Ent. France, (2) 5: 407.
Europe.
"Ichneumon rubens Wesmael"': Rudow, 1918. Ent. Ztschr. Frankfurt,
32: 72. Hosts: Cerura vinula, Lymantria dispar.
Protichneumon rubens: Gy6rfi, 1963. Kiilonl Allattani Kozlem, p. 50-53.
Host: Lymantria dispar (of minor importance).
Pavacoelichneumon rubens: Heinrich, 1978. Eastern Palaearctic iennetie
moninae (in Russian), Acad. Sci. USSR, p. 14.
This species has been referred to as Ichneumon rubens Wesmael in the
gypsy moth literature (Stadler, 1933, Schedl, 1936). It was apparently first
associated with the gypsy moth by Rudow (1918). Gyorfi (1963) mentioned
having reared it in Hungary from the same host. Other host records in litera-
ture are of Cerura vinula and Catocala elocaita in Europe.
Flagellum of the female a little widened and ventrally flattened preapically.
Face punctate, punctures denser in the median area. Clypeus with scattered
punctures at base, smoother apically, its apical margin arcuate. Malar space
0.85 as long as basal width of mandible. Mesoscutum subpolished, with
V. Gupta: Gypsy Moth Parasites 89
scattered but definite punctures. Scutellum flat, polished and with scattered
punctures. Apex of scutellum in level with the metascutellum. Mesopleurum
with distinct large punctures, well separated from each other, by at least
their diameter. Metapleurum striato-punctate. Propodeum rugose. Petiolar
area and third lateral area trans-rugose. Postpetiole rugulose, its median
area weakly defined. Abdomen regularly punctate. Gastrocoeli wide and deep,
interspace between gastrocoeli 0.7 their width. Apex of female abdomen acute.
Black with reddish abdomen. Vertical orbits, scutellum, subtegular ridge
and a median band on flagellum yellow. Frontal orbits finely marked with
brown. Hind corner of pronotum and tegula brown to brownish-black. All
coxae and trochanters black. Hind tarsus brownish-black. Legs otherwise
reddish (brick-red) with apices of hind femur and tibia blackish. Abdomen
from second segment onwards reddish. Wings hyaline, very slightly infuscated.
Length: 20mm. Fore wing 14 mm.
Specimens: One female from Rumania in the Townes Collection examined.
No reared specimens seen.
Distribution: Europe.
3. Genus CALLAJOPPA
Callajoppa Cameron, 1903. Entomologist, 36: 236.
The genus Callajoppa is characterized by having the mandible not tapered
apically, its lower tooth about 0.5 as long as the upper, occipital carina joining
hypostomal carina before the base of mandible, female flagellum widened
preapically, scutellum pyramidal, without sharp angles, areola in the form of
a polished raised "boss"', somewhat pyramidal in profile, postpetiole flat and
with scattered punctures, gastrocoeli shallow, with the interspace between
them as wide or wider than the width of a gastrocoelus, and apex of female
abdomen obtuse.
Only one species, Callajoppa cirrogaster cirrogaster (Schrank) is associ-
ated with the gypsy moth. This has generally been referred to as Ichneumon
lutorius or Trogus lutorius,
1. CALLAJOPPA CIRROGASTER CIRROGASTER (Schrank) (Figs. 91-94)
Ichneumon cirrogaster Schrank, 1781. Eunmeratio Insectorum Austriae.
Indigenorum, p. 348. Europe.
Ichneumon lutorius Fabricius, 1787. Mantissa Insectorum. .., 1: 262.
Italy.
Trogus lutovius:Mocsary, 1787. Tijdschr. Ent., 21: 198. Russia.
"Trogus flavitorius [sic] lutorius (Fab.)?'": Howard and Fiske, 1911.
U.S.D.A. Bur. Ent. Bull., 91: 85. Host: Lymantria dispar.
Europe. |
Trogus lutorius: Meyer, 1933. Tables systematiques des hymenoptéres
parasites (fam. Ichneumonidae) de 1'URSS et des payes limitrophes,
1: 345. Russia. Europe. Hosts: Papilio machaon, Dendrolimus
pint, Lymantria dispar.
Callajoppa cirrogaster cirrogaster: Townes, Momoi and Townes, 1965.
Mem. Amer. Ent. Inst., 5: 539. Europe. Russia.
90 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
This species was first mentioned as a parasite of the gypsy moth by Howard
and Fiske (1911, reference cited above), based upon the information they had
on their card file as well as from Dalla Torre (1901-02). No such host record
is, however, seen in Dalla Torre under "Iutorius’’. Other persons who reported
this species as a parasite of the gypsy moth are Meyer (1933) and subsequent
catalogers like Stadler, Schedl and Thompson. Townes, Momoi and Townes
considered Tvrogus lutorius as a synonym of Callajoppa cirrogaster cirrogaster.
A subspecies, C. cirrogaster bilineata Cameron occurs in China and Japan.
Its hosts are species of Laothoe, Smerinthus, and Dendrolimus. C. ctirrogas-
ter caspica Heinrich occurs in Iran and Transcaucasia.
Face and clypeus punctate. Punctures coalescing in the median area of
face. Malar space ruguloso-mat, 1.15 as long as basal width of mandible.
Antennal scrobes concave and polished. Vertex concave behind. Temple
widened medially. Female flagellum a little indented preapically and then
tapering. Mesoscutum finely punctate on a mat surface. Scutellum subpolished
pyramidal, without lateral margins or angles. Side of thorax largely punctato-
striate. Upper half of pronotum and mesopleurum punctate. Propodeum with
areola in the form of a polished elevated "boss", whence with a straight slope
to the abdominal attachment. Costula, and median and lateral longitudinal
carinae strong and raised. Propodeum strongly transcarinate, especially in
the female. Petiole long, narrow and squarish in cross section. Postpetiole
wide and flat, weakly punctate, its median field not sharply demarcated. Abdo-
men finely punctate, obtuse apically. Gastrocoeli shallow and broad, the inter-
Space between them as wide as the width of gastrocoeli and aciculate.
Black with yellowish-brown abdomen. Face, clypeus, mandible except
teeth, lower temple, inner and outer orbital borders, and ocellocular area
yellowish-brown. Frons, ocellar patch, vertex and temple posteriorly, and
occiput, black. The extent of yellowish-brown on outer orbits variable and in
some males may not be connected to inner orbits dorsally. Antenna yellowish-
brown. Thorax black with yellow marks on upper part of pronotal collar, upper
margin of pronotum, hind corner of pronotum, tegula, subtegular ridge, scutel-
lum, metascutellum, and a mark along lateral carina of scutellum. Mesoscutum
sometimes with a reddish-brown mark. Legs brownish, with all coxae black,
and fore coxa yellowish apically. Hind femur with blackish marks. Tarsi
lighter in color. Wings yellowish-brown. Petiole blackish basally. Apex of
abdomen black or brown.
Length: 22-24mm. Fore wing 16-18 mm.
Specimens from Europe seen in the Townes Collection, ex pupa of "Amorpha
tremulae".
Distribution: Eurasia.
Hosts: Lymantria dispar, Papilio machaon, Dendrolimus pini and Amorpha
tremulae. Thompson (1957) lists several others belonging to the family
Sphingidae.
4, Genus ICHNEUMON (Fig. 114)
Ichneumon Linnaeus, 1758. Systema Naturae, (Ed. 10), 1: 560.
= Coelichneumon of authors.
This genus is characterized by having a bristle-shaped flagellum, more or
less widened preapically in the female, apical margin of clypeus arcuate or
truncate, a little impressed, occipital carina joining hypostomal carina, man-
V. Gupta: Gypsy Moth Parasites 91
dible moderately narrowed apically, propodeum convex on basal half or less,
areola usually horse-shoe shaped or hexagonal, often confluent with basal
area, not raised above the general surface of propodeum, abdomen spindle-
shaped, a little narrower than the thorax, black or bluish-black, with or without
white spots. Postpetiole usually with a distinct aciculate median area, and
geastrocoeli large and deep, sometimes wider than the space between them.
The tip of abdomen in the female is strongly acute, pointed (oxypygous).
Several species of Ichneumon have been reported in literature as parasites
of the gypsy moth. There appear to be many erroneous records. The
identities of some of the species are also not clear. It appears that only
Ichneumon cyaniventris may be a parasite of the gypsy moth.
1. ICHNEUMON CYANIVENTRIS Wesmael
Ichneumon cyaniventris Wesmael, 1859. Mém. Couronnés Acad. Sci.
Belgique, 8: 58. Europe.
Ichneumon cyaniventris Wesm.: Rudow, 1918. Ent. Ztschr. Frankfurt,
32: 59. Europe. Host: Lymantria dispar.
Ichneumon cyaniventris Wesmael: Townes, Momoi and Townes, 1965.
Mem. Amer. Ent. Inst., 5: 523. Eurasia, Korea, Japan. Host:
Closteraanastomosis (in Japan).
This species was listed by Rudow (1918) as a parasite of the gypsy moth,
Lymantria dispar. He did not list it in 1911 in his list of parasites of various
"Bombycidae’"’". Subsequent catalogers have somehow missed this and some
other species listed by Rudow.
This species is rather closely related to Ichneumon sugillatorius L. from
Lymantria monacha. Both have similar color patterns with white spots on
abdominal tergites. The face of male is white with a wide black vertical line,
which is wider in cyaniventris than in sugillatorius. The areola of cyaniventris
is flat and propodeum a little sloping, while in sugillatorius, the areola is a
little raised and propodeum convex in this area.
Ichneumon leucocerus Gravenhorst is different in having no white spots on
the abdomen and the propodeum convex in the region of areola. The areola is
crescentic, narrower than in cyaniventris or sugillatorius.
Some of the salient features of this species are:
Face and clypeus punctate. Clypeus flat and a little arcuate apically. Sub-
apical segments of female flagellum a little widened and flattened ventrally.
Flagellum apically tapered. Mandible apically not strongly tapered. Thorax
punctate. Scutellum flat, shiny, with scattered punctures. Areola horse-shoe
shaped, a little wider than long, its apical closing carina concave. Propodeum
rugose or rugoso-punctate, with areola smoother. Propodeum in the region of
areola flatter and sloping or in male a little convex. Postpetiole aciculate.
Petiole laterally margined and trans-striate. Second tergite medially aciculate
rest punctate to striato-punctate. Gastrocoeli deep. Thyridia wide, their
interspace 0.7 the width of each thyridium. Abdomen apically acute, punctate,
punctures progressively smoother apically.
Black. Face of male white laterally, rather broadly so. Flagellum with
about five medial segments wholly or partly white. Scutellum yellow. Ter-
gites 2-3 in ¥ and 2-4 in male with apicolateral white spots. Fore tibia with a
yellowish-brown line. In male fore and middle legs from apex of femur on-
wards brownish, or with yellowish-brown patches. Thorax of male with yellow
?
92 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
marks along upper margin of pronotum, on tegula and on subtegular ridge.
Length: 15-16 mm. Fore wing 11 to 12 mm.
Specimens from Germany seen in the Townes Collection, but no reared
specimens were available.
Distribution: Eurasia, Japan and Korea.
2. ICHNEUMON LEUCOCERUS Gravenhorst
Thompson (1946) listed this species as a parasite of Lymantria dispar
quoting Stadler (1933) and Schedl (1936) from Europe and North Africa.
Stadler (1933: 30) however mentioned 'Tchneumon leucocherrus Wesmael"' as a
parasite of Lymantria dispar, and not Ichneumon leucocerus Gravenhorst,
which was quoted as such by Schedl (1936). How the record got converted into
leucocerus is not clear.
"Ichneumon leucocherrus Wesm." is not listed in Dalla Torre (1901-02), nor
could I find this name in any other publication. It was obviously a lapsus, not
for Ichneumon leucocerus Gravenhorst as Thompson apparently thought, but
for Ichneumon leucocheilus,Wesmael as this latter species was reported para-
sitic upon Lymantria dispar by Rudow (1918).
Ichneumon leucocheilus Wesmael properly belongs to the genus Melanichneu-
mon (authentic specimens not available).
Ichneumon leucocerus Gravenhorst is to be removed from the list of para-
sites of the gypsy moth.
3. "ICHNEUMON PICTUS Gmelin”
Ichneumon pictus Gmelin, 1790. In Linnaeus: Syst. Nat., Ed 13,1(5): 2721.
Ichneumon pictus Gmelin: Dalla Torre, 1901-02. Catalogus Hymenopter-
orum, 3: 968. Eurasia (in part).
The identity of this species is uncertain. Infact Gmelin (1790. Systema
Naturae) described two 'Tchneumon pictus", --one on page 2702 and another
on p. 2721. The one described on page 2702 was synonymized under Micro-
cryptus sericans (Gravenhorst) (Gelinae) by Dalla Torre (1901-02: 708). The
other, described on page 2721, was considered by Dalla Torre (1901-02: 968)
to be a senior synonym as well as a homonym of Ichneumon pictus Gravenhorst
(1829: 418)|which was actually described as Hoplismenus pictus Gravenhorst].
A perusal of the original descriptions of the above two species indicates
that they are not synonymous.
Hoplismenus pictus Gravenhorst is Stenoblus pictus (Gravenhorst) vide
Rasnitsyn (1981: 132) and Kaspayran (1981: 580). The identity of ‘‘Jchneumon
pictus Gmelin, 1790: 2721" can not now be established. Subsequent workers
have overlooked this species. It is incidentally a junior primary homonym of
Ichneumon pictus Schrank, 1776, as well as a homonym. of Ichneumon pictus
Gmelin 1790: 2702.
Berthoumieu (1895), in his treatment of the European Ichneumonidae did
not mention J, pictus of Gmelin. He mentioned J, pictus Gravenhorst (= rufes-
cens Stephens = vaizeburgi Hartig) and mentioned Lymantria dispar as a host
of it upon the authority of Mocsary (1885). Mocsary's references could not be
located.
Ichneumon pictus Gmelin, should therefore be removed from the list of the
V. Gupta: Gypsy Moth Parasites 93
parasites of the gypsy moth.
Ichneumon pictus (Gravenhorst) is treated here under Stenaoplus. Records
of Ichneumon pictus Gmelin as a parasite of Lymantria dispar, as given by
Stadler (1933), Schedl (1936) and by Thompson (1946, p. 495), should be con-
strued to belong to Stenaoplus pictus (Gravenhorst).
The entry in Thompson (1946, p. 499) as Stenichneumon pictus Gmelin also
pertains to Stenaoplus pictus (Gravenhorst). Thompson cited Morley and Rait-
Smith (1933) as his source of information. Morley and Rait-Smith referred to
Stenichneumon pictus Gravenhorst and not Gmelin, taking the host record from
Morley (1903, 1: 49).
4. "ICHNEUMON FLAVUS Rd." Nomen nudum.
"Ichneumon flavus Rd.": Rudow, 1918. Ent. Ztschr. Frankfurt, 32: 64.
Europe. Hosts: Lymantria dispar, Cerura vinula.
"Ischnus flavus Rd."': Stadler, 1933. Ent. Anz., 13(2-4): 30.
I could not trace the original description of this species in Rudow's publica-
tions, nor in Zoological Record. How the generic name changed from Ichneu-
mon to Ischnus in subsequent publications of Stadler (1933) and Schedl (1936) is
unclear. Thompson (1946) mentioned it as 'Ischnus flavus Rond."
Rudow apparently intended to describe it as a new species. It is a nomen
nudum.
5. ICHNEUMON sp.
"Ichneumon sp.": Picard, 1921. Progres Agric. Vitic., 76(33): 160-165.
France. Schedl, 1936: 188. Thompson, 1946: 495. Host: Lymantria
dispar.
The identity of this species will remain uncertain until the voucher speci-
men is seen, if still available. It could be one of the other Ichneumonini
treated here.
TRIBE JOPPINI
0. Genus STENAOPLUS
Stenaoplus Heinrich, 1938. Mem. Acad. Malgache, 25: 116.
The genus Stenaoplus is characterized by having a moderately to strongly
raised scutellum which is laterally sharply margined by carinae up to its apex,
flagellum of female long, tapering and slender, not flattened or much widened
preapically, propodeum flat on basal half and then sloping, the horizontal por-
tion of propodeum a little shorter than the apical sloping part, apophyses absent,
areola normally formed, squarish or elongate, postpetiole granulose to punc-
tate, without a median field, gastrocoeli Shallow, weakly impressed, very
wide, and narrow, the space between them less than 0.7 their width.
One species, Stenaoplus pictus (Gravenhorst) has been mentioned in litera-
94 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
ture as a parasite of the gypsy moth.
1. STENAOPLUS PICTUS (Gravenhorst)
Hoplismenus pictus Gravenhorst, 1829. Ichneumonologia Europea, 2: 418.
Ichneumon pictus Gravenhorst: Berthoumieu, 1895. Ann. Soc. Ent.
France, 1895, p. 567. (synonymy and host records).
Ichneumon pictus: Dalla Torre, 1901-02, Catalogus Hymenopterorum,
3: 968. (Inpart). Hosts: Lymantria dispar (after Mocsary),
Thera juniperata, Semiothisa liturata, Cidaria fulvata.
Ichneumon rufescens Stephens, 1835. Illustrations to British Entomology,
Mandibulata, 7: 207. Name preoccupied by Rossi, 1794 and by
Cervier, 1833.
Cryptus Ratzebergi Hartig, 1838. Jahresber. Forstschr. Forstw.,
1 (2): 263. Host: Dendrolimus pini.
Ichneumon rufescens Stephens: Perkins, 1953. Bull. British Mus. (N.H.)
Ent., 3:112. [= Aoplus ratzeburgi (Hartig), syn. Stenichneumon
pictus (Gravenhorst) Morley. ]
Hoplismenus pictus Gravenhorst and Ichneumon pictus Gmelin are not pri-
mary homonyms and do not belong to the same genus now. Therefore the
name pictus Gravenhorst is reinstated for rufescens Stephens or vatzeburgi
Hartig, as used in the publications of Perkins (1953, 1960) and Fitton (1978).
Stenaoplus pictus (Gravenhorst) was first reported as a parasite of the
gypsy moth by Mocsary (1885). Berthoumieu (1895) mentioned it in his treat-
ment of the European Ichneumoninae. All the reports of Stadler, (1933), Schedl
(1936) and Thompson (1946, p. 495 and 499), pertain to this species. The host
records as given by Morley (1903) and others are Lymantria dispar, Cidavria
fulvata, Semiothisa liturata and Thera juniperata. Kasparyan (1981) mentions
these hosts except Lymantria dispar —the reason for which is not stated! Per-
kins (1960) stated that this species is parasitic on geometrids on Pinus.
Female: Small sized species. Subapical flagellar segments not conspicu-
ously widened though a little flattened ventrally. Face and Clypeus with distinct
well separated punctures. Clypeus a little convex basally, its apical margin
truncate. Mandible narrowed apically, its lower tooth short and pointed.
Malar space about 0.8 as long as the basal width of mandible. Temple not
widened medially. Mesoscutum mat, with shallow punctures. Scutellum sub-
convex, laterally carinate and with scattered minute punctures. Mesopleurum
and metapleurum punctate. Areola horse-shoe Shaped, as long as wide, sub-
polished, mat. Petiolar area concave. Postpetiole mat. Tergites 2 and 3
with definite regular punctures. Thyridia wide, about 2.0 as wide as the space
between them. Ovipositor rather long for the group, as long as or longer than
the maximum width of abdomen (apical width of tergite 2).
Brownish-yellow. Frontal and vertical orbits yellow marked. Frons,
vertex, occiput and antenna blackish-brown. Apex of scutellum, metascutel-
lum, and subtegular ridge yellow-marked. Propodeum blackish. Coxae brown-
ish with dorso-apical blackish marks. Hind tibia and tarsus with fuscous spots.
Abdomen brownish-yellow, without any white apical marks.
Male: Face strongly punctate. Body conspicuously marked with red and
yellow. Inner orbits yellow. All femora reddish. Hind tibia without a yellow
median band. Coxae usually marked with yellow and red.
Length: 6-10 mm. Fore wing 4.5-6.5 mm.
V. Gupta: Gypsy Moth Parasites 95
Specimens: England, 1%, det. Perkins, 1953 (Townes). No reared speci-
mens seen.
Perkins (1960) puts the species under Aoplus as vatzeburgii (Hartig) and
provides a key to distinguish it from the other British species.
6. Genus MELANICHNEUMON (Fig. 115)
Melanichneumon Thomson, 1893. Opuscula Entomologica, 18: 1954.
The genus Melanichneumon is characterized by having the subapical flagel-
lar segments of the female very wide and flat ventrally, the widest segments
about 2.0 as wide as long. Male flagellum with transverse ridges ventrolater-
ally which are beset with short bristles. Base of propodeum with a small
median tubercle. Areola more or less horse-shoe shaped, narrowed towards
base. Propodeal carination sharp and of a generalized type. Abdominal ter-
gites 2-3 strongly neatly punctured and convex. Postpetiole also punctate, not
striate. Thyridia weakly impressed, the space between them more than 1.9
the width of a thyridium. Apex of female abdomen oxypygous, and usually
yellow or white.
One species of this genus has been mentioned as a parasite of the gypsy
moth, under the name Ichneumon leucocheilus Wesmael.
1. MALANICHNEUMON LEUCOCHEILUS (Wesmael) (Figs. 95, 96)
Ichneumon leucocheilus Wesmael, 1844. Nouv. Mem. Acad. Sci. Bouxelles,
18: 89. Europe.
Ichneumon leucocheilus Wesm.: Rudow, 1918. Ent. Ztschr., 32: 64.
Europe. Host: Lymantria dispar.
Melanichneumon leucocheilus: Perkins, 1960. Handbook for the identifica-
tion of British Insects, 7(2): 150. England.
The earliest reference to this species being parasitic upon Lymantria
dispar was traced to Rudow (1918).
"Ichneumon leucocherrus Wesm.'' as quoted by Stadler (1933) and Schedl
(1936) is definitely a lapsus for]. leucocheilus Wesm. No species as
"Ichneumon leucocherrus Wesm."' exists. Thompson (1946) erroneously
reported it as 'Jchneumon leucocerus Gravenhorst."'
Specimens of this species were not available for study. The following
description is taken from Berthoumieu (1895) and Perkins (1960):
Clypeus with a weak, rather broad, central projection. Areola sub-
hexagonal, elongate. Legs robust. Postpetiole punctate. Gastrocoelus small
and superficial. Thyridium indistinct. Occipital carina meeting hypostomal
carina near base of mandible.
Female: Antenna with a white annulus. Head and thorax wholly black.
Wings hyaline. Stigma black. Tegula reddish-brown. Legs reddish-brown with
coxae black. Hind femur and tibia brown. Abdominal segments 2-4 and base of
0, reddish-brown. 6-7 segments white. Tip of abdomen white.
Male: Facial orbits white. Antenna black, ferruginous basally. Wings a
little infuscate. Coxae and trochanters black. Rest of fore and middle legs
red, with white or fuscous patches. Hind femur infuscate, tibia and tarsus
black. Abdomen black with apex of tergites 1-3 red. Tergite 7 with a large
96 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
dorsal white spot.
Length: 10-13 mm.
Distribution: Europe.
7. Genus CRATICHNEUMON (Fig. 117)
Cratichneumon Thomson, 1893. Opuscula Entomologica, 18: 1945.
Female flagellum cylindrical and blunt apically, only a little widened pre-
apically. Occipital carina joining hypostomal carina at a distance equal to
0.35 the basal width of mandible. Scutellum flat, not carinate laterally.
Median part of propodeum without a weak tubercle in the middle, its dorsal
surface flat, and petiolar area excavated. Postpetiole with shallow punctures,
or its median area with only fine striations and not sharply demarcated from
the lateral areas. Gastrocoeli weak, superficial. Thyridia linear, smaller
than the distance between them. Abdomen oxypygous.
Cratichneumon is close to Melanichneumon. Species of Cratichneumon are
more smooth and shiny, with less densely punctate mesoscutum and abdomen,
shallower gastrocoeli, which are often obsolete, and abdominal tip is rarely
white marked.
Members of this genus are generally parasitic upon geometrid pupae.
The females do not hibernate and many species have two generations per year,
adults appearing in May-June and again in August. One species, Ichneumon
fabricator, is reported in the literature as a parasite of the gypsy moth.
1. CRATICHNEUMON FABRICATOR (Fabricius) (Fig. 97, 98)
Ichneumon fabricator Fabricius, 1793. Entomologica Systematica, 2: 166.
Germany.
Ichneumon fabricator F.: Schedl, 1936. Monogr. Angew. Ent., 12: 188.
Europe. Hosts (after Cecconi, 1924): Lymantria dispar, Elkneria
pudibunda, Panolis flammea, Bupalus piniaria, Operophtera brumata.
Protichneumon fabricator: Gyorfi, 1963. Kulonenyomet az allattani
Kozleményeh L. Kotet, 1-4: 51. Hungary. Not common. Host:
Lymantria dispar.
Cratichneumon fabricator: Townes, Momoi and Townes, 1965. Mem.
Amer. Ent. Inst., 5: 442. Eurasia.
Cratichneumon fabricator: Kasparyan, 1981. Fauna USSR, Vol 3 (Ichneu-
monidae): 573. Eurasia. Hosts: Semiothisa liturata, Bupalus
piniavria, Rhyacionia pinicolana, Notodonta dromedarius, Elknevria
pudibunda, Panolis flammea, and Tethea or.
This species was first reported from Lymantria dispar by Cecconi (1924).
Kasparyan (1981) listed several hosts in European USSR, but did not mention
Lymantria dispar . |
Female: Flagellum cylindrical and blunt apically, only a little widened pre-
apically. Face a little convex below antennal sockets. With well separated
punctures. Clypeus polished, with rows of punctures at base and with a few
scattered punctures in the middle. Temple wider ventrally. Malar space
equal to the basal width of mandible. Frons and vertex mat, with scattered
punctures. Vertex widened behind eyes. Thorax punctate, the mesoscutum
V. Gupta: Gypsy Moth Parasites 97
shallowly so and propleurum more densely so. Scutellum flat, subpolished and
with scattered punctures. Propodeum flat dorsally, its petiolar area excavated.
Lateral carinae of areola indistinct basally. Median field of postpetiole not
sharply demarcated, with fine weak striations interposed with punctures.
Tergite 2 punctate. Width of thyridia less than the distance between them.
Tergite 3 with shallow, indistinct punctures.
Black. Flagellum with a white annulus. Tegula brownish-black. All
coxae and trochanters black, femora brown, tibiae brown with white marks
and tarsi brown. Hind tibia apically and tarsus darker, brownish-black.
Wings hyaline, a little brown-tinged.
Male: Flagellum tapered, somewhat serrate. Propodeal carinae stronger.
Postpetiole without striations. Gastrocoeli deeper.
Face and clypeus largely white. Face with a black central mark. Flagel-
lum brownish below, without a white annulus. Hind corner of pronotum and
subtegular ridge yellow. Fore and middle femora, tibiae and tarsi orange
colored. Hind leg wholly brownish-black.
Length: 8-11 mm. Fore wing 7-8 mm.
Specimens from Europe examined in the Townes Collections. No reared
specimen seen. Several host records are mentioned by Thompson (1957).
Distribution: Europe.
8. Genus CHASMIAS (Fig. 118)
Chasmias Ashmead, 1900. Proc. U. S. Natl. Mus., 23: 17.
Apical margin of clypeus broadly weakly concave, with a weak broad
median tooth. Mandible not much narrowed apically, its lower tooth shorter
than the upper. Occipital carina joining hypostomal carina above the base of
mandible. Antennal flagellum cylindric in the female and somewhat serrate in
the male. Preapical segments not flattened. Tip of female flagellum blunt
and apical segments curled. Areola horse-shoe shaped, open behind, elongate
in female. Abdomen oxypygous. Postpetiole with a weak median field, which
is weakly striate. Gastrocoeli small to large, shallow. Ovipositor distinctly
exserted beyond the tip of abdomen.
One species, Chasmodes paludicola, was reported by Rudow (1917) as a
parasite of the gypsy moth in Europe.
1. CHASMIAS PALUDATOR (Desvignes)
Ichneumon paludator Desvignes, 1854. Trans. Roy. Ent. Soc. London,
(N.S.) 3: 44. England.
Chasmodes paludicola Wesmael, 1857. Bull. Acad. Sci. Belgique,
(2)2: 356. Europe.
Chasmias paludicola: Dalla Torre, 1901-02. Catalogus Hymenopterorum,
3: 1024.
Chasmodes paludicola: Rudow, 1917, Ent. Ztschr. Frankfurt, 31: 31.
Host: Lymantria dispar.
Heinrich (1937) synonymized Chasmodes paludicola with paludator.
Rudow's record was missed by Schedl, Thompson and others.
Female: Face with distinct well separated punctures, interspaces 1.0 to
98 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
1.5 the diameter of the punctures and shiny. Thorax punctate. Punctures on
-mesoscutum small and shallow. Scutellum flat, subpolished. Areola horse-
shoe shaped, open behind, elongate in the female. Median field of postpetiole
very finely striate. Gastrocoeli small. Tergites 2 and 3 finely punctate.
Ovipositor extending conspicuously beyond the tip of abdomen.
Black. Flagellum medially and scutellum yellow. Coxae black. Legs
otherwise reddish-brown, with tarsi infuscate. Tergites 1, 2, and 3 reddish-
brown, the rest black. Tergite 7 with an elongate yellowish-brown longitudinal
stripe.
Male: Punctures stronger over body. Flagellum tapered and weakly
serrate. Areola more squarish and widely open behind.
Black. Facial orbits narrowly yellow. Scutellum black. All femora,
and tibiae reddish-brown, tarsi infuscate. Tergite 2 largely reddish-brown,
with black patches, rest of abdomen black.
Length: 15-17mm. Fore wing 12-14 mm.
Specimens from Europe examined in the Townes Collections. No reared
specimens seen.
Distribution: Europe.
9. Genus PTEROCORMUS (Fig. 120)
Pterocormus Foerster, 1850. Arch. f. Naturgesch., 16: 71.
= Ichneumon of authors.
A genus close to Chasmias, but apical margin of clypeus truncate, or
weakly convex, without a median tooth, apical part of female flagellum more
or less tapered, thyridia moderately large and distinctly impressed and
median fold on sternite 4 rather distinct.
One species, Ichneumon sarcitorius was recorded by Meyer (1929) as a
parasite of the gypsy moth in Russia.
1. PTEROCORMUS SARCITORIUS SARCITORIUS (Linnaeus) (Figs. 99, 113, 120)
Ichneumon sarcitorius Linnaeus, 1758. Systema Naturae, (Ed 10) 1: 561.
Europe.
Meyer, 1929. Rpts. Sppl. Ent., Bur. Appl. Ent., State Inst. Exper.
Agron, Leningrad, 4: 240. Host: Lymantria dispar. USSR.
Pterocormus sarcitorius sarcitorius: Townes, Momoi and Townes, 1965.
Mem. Amer. Ent. Inst., 5: 479. Syn. references, host records.
Eurasia. North Africa.
Female: Face punctate, interspaces shiny. Flagellum cylindrical, apical
segments tapering and weakly curled. Thorax punctate. Scutellum flat and
subpolished. Punctures on meso-and metapleurum becoming rugose at places.
Propodeum ruguloso-punctate. Areola squarish, open behind. Median field of
postpetiole clearly demarcated and finely longitudinally striate. Gastrocoeli
small but deep. Tergite 2 and 3 moderately deeply punctate. Sternites 2-5
with a midventral fold. Ovipositor slightly exserted beyond abdominal tip.
Black. Frontal orbits, and tegula brown. Median flagellar segments,
subtegular ridge and scutellum yellow. All coxae, trochanters and apices of
hind femur and tibia black. Legs otherwise reddish-brown. Tergite 2 wholly
V. Gupta: Gypsy Moth Parasites 99
and tergite 3 in apical 0.6 reddish-brown. Sternites 2 and 3 yellowish-brown.
Tergite 6 broadly yellow dorsally.
Male: Face, clypeus and scape ventrally yellow. Clypeus and face tri-
angularly above clypeus may be black. Antenna brown, darker dorsally.
Tegula, subtegular ridge and scutellum, yellow. Hind corner of pronotum also
often yellow. Apices of abdominal tergites yellow, these yellow marks widened
laterally. Those on tergites 1 and 4 usually incomplete dorsally, and absent
on tergite 5.
Length: 12-16mm. Fore wing 9-12 mm.
Specimens from Europe examined in the Townes Collections. No reared
specimens seen.
Distribution: Eurasia, China, North Africa.
Hosts: Lymantria dispar, Diloba caeruleocephala, Gortyna borelli, and
Agrotis segetum.
10. Genus TRIPTOGNATHUS (Fig. 119)
Triptognathus Berthoumieu, 1904. Genera Insectorum, 18: 49.
Female flagellum short, curled, its second segment 0.8 to 1.4 as long
as wide, its apex with a short taper. Flagellum of male slender. Mandible
not tapered apically, only slightly narrowed apically. Occipital carina joining
hypostomal carina above base of mandible. Areola about 1.0 as long as wide.
Abdomen amblypygous, its tip rounded. Side of median field of postpetiole
sharply detined. Gastrocoeli small to large, shallow to moderately deep, with
a distinct thyridium. Sternite 3 with its median 0.3 or more membranous,
visible as a longitudinal fold in dried specimens. Sternite 4 not membranous
medially. Ovipositor unusually short. Female subgenital plate conspicuous.
Male subgenital plate with a rather long median apical lobe. Genital claspers
unusually large, in profile view the lower apical corner more produced and
pointed than the upper.
One species, Triptognathus amatorius (Mueller), is associated with the
gypsy moth.
1. TRIPTOGNATHUS AMATORIUS (Mueller) (Figs. 100-103)
Ichneumon amatorius Mueller, 1776. Zoologicae Danicae Prodromus,
p. 151. Denmark.
Amblyteles amatorius: Rudow, 1917. Ent. Ztschr. Frankfurt, 31: 26.
Europe. Hosts: Lymantria dispar, L. monacha.
Amblyteles amatorius: Uchida, 1926. J. Fac. Agr. Hokkaido Imp. Univ.,
18: 118. Sakhalin. Hosts: Lymantria dispar, L. monacha,
Anaplectoides virens, Dendrolimus albolineatus.
Triptognathus amatoria: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 496. Europe, Japan, Russia, Sakhalin.
Diphyus amatorius: Kasparyan, 1981. Fauna USSR, Ichneumonidae,
3: 614, 616, 617, 618. Russia.
This species was not listed as a gypsy moth parasite by Schedl (1936) or
Thompson (1946). The earliest record of its occurrence on the gypsy moth
is that of Rudow (1917) in Europe and Uchida (1926) in Sakhalin.
100 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Female: Face densely punctate. Mesoscutum closely finely punctate.
Scutellum flat, subpolished with shallow indistinct punctures. Mesopleurum
and metapleurum densely punctate, punctures on metapleurum finer than those
on mesopleurum. Propodeum densely finely punctate. Areola rectangular,
open behind. _Costula indistinct. Apophyses indistinct. Median field of post-
petiole longitudinally striate. Postpetiole punctate apicolaterally. Tergites
2 and 3 very finely and closely punctate. Gastrocoeli weakly impressed,
rather indistinct, their width less than the space between them. Ovipositor
hardly exerted.
Black. Inner orbits, flagellum medially, hind corner of pronotum, sub-
tegular ridge and scutellum yellow. Apices of abdominal tergites yellow.
Tergite 2 orange-red. Sternites 2 and 3 orange-red. Legs black with their
femora and tibiae yellowish-brown. |
Male: Generally similar to the female but flagellum long and slender,
black. Punctures on face more regular and a little larger. Thoracic punc-
tures comparatively larger. Areola squarish, closed behind and gastrocoeli
more distinctly impressed. Sternites 2 and 3 with a midventral fold.
Face, clypeus and scape ventrally, yellow. Tegula, subtegular ridge,
hind corner of pronotum and scutellum, yellow. Legs as in the female but fore
femur wholly, and middle femur largely also yellow. Tergites 2 and 3 yellow.
Yellow margins on tergites narrow.
Length: 15-18 mm. Fore wing 12-15 mm.
Specimens from Europe seen in the Townes Collection. No reared speci-
mens seen.
Distribution: Eurasia.
11. Genus SPILICHNEUMON _ (Fig. 116)
Spilichneumon Thomson, 1894. Opuscula Entomologica, 19: 2087.
Female flagellum short, curled, its second segment about 1.4 to 1.8 as
long as wide, its apex with a short taper. Mandible wide, apically, in male
gradually tapered. Male flagellum with a long taper. Areola about 1.4
(male) or 1.8 (female) as long as wide. Apical half of postpetiole with the
median field indistinctly bounded laterally. Abdomen amblypygous. Oviposi-
tor unusually short. Sternite 4 often not membranous medially. Subgenital
plate of male and female and male claspers as in Tviptognathus.
One species, Ichneumon occisor Fabricius, was listed by Rudow (1917) as
a parasite of the gypsy moth in Europe.
1. SPILICHNEUMON OCCISOR (Fabricius) (Figs. 104-110, 116)
Ichneumon occisor Fabricius, 1793. Ent. System., 2: 142. Europe.
Ichneumon occisorius Fabricius, 1804. System. Piez., p. 61.
Emendation. ,
Amblyteles occitsorius Wesm: Rudow, 1917. Ent. Ztschr. Frankfurt,
31: 26. Hosts: Lymantria dispar, Leucoma salicis.
Spilichneumon occisor: Townes, Momoi and Townes, 1965: 504.
(= occisorius Grav. = occisor Fabr.)
Rudow (1917) apparently first recorded it as a parasite of Lymantria
V. Gupta: Gypsy Moth Parasites 101
dispay. Subsequent cataloguers have missed this species in their lists.
This species resembles Triptognathus amatorius and Pterocormus
sarcitorius in general appearance, but it can be readily separated from them
by the characters given in the keys above.
Female: Face with minute well formed punctures, interspaces shiny.
Clypeus rather flat. Mandible a little wider preapically. Thorax punctate
with mesoscutum finely so and largely shiny. Scutellum polished. Propodeum
finely ruguloso-punctate. Areola elongate and narrow, rounded basally. Post-
petiole finely aciculate in the median field, polished otherwise. Tergites 2
and 3 very finely and shallowly punctate and shiny. Sternites 2 and 3 witha
median fold.
Black. Frontal orbits and mandible reddish-brown. Flagellum yellowish-
brown subapically. Subtegular ridge yellow. Scutellum yellow. Tergites and
sternites 2 and 3 orange-red. Other tergites yellow medially along their api-
cal margins, these stripes incomplete. Legs blackish-brown with tibiae and
tarsi lighter in color.
Male: Face, clypeus, mandible medially, and underside of scape, yellow.
Tegula, subtegular ridge, hind corner of pronotum and scutellum, yellow.
Legs yellow with all coxae and trochanters and hind femur black. Apex of
hind tibia black. Abdomen black with tergites 2 and 3 largely and apices of
the following tergites, yellow. Last tergite largely yellow. Only sternite 2
with a median fold.
Length: 12-15mm. Fore wing 8-10 mm.
Specimens from Europe in the Townes Collection examined. No reared
Specimens seen.
Distribution: Europe.
12. Genus AMBLYTELES
Amblyteles Wesmael, 1844. Nouveaux Mém. Acad. Roy Sci. Lett.
Beaux-Arts Belgique, 18: 112.
Apical margin of clypeus truncate, without any tubercle. Lower tooth
of mandible small. Occipital carina complete to hypostomal carina. Flagellum
long, its second segment 1.4 to 3.0 as long as wide, its apex tapered, median
segments cylindric. Propodeum with distinct sublateral triangular projections,
one on either side. Abdomen of female amblypygous, its tip blunt. Gastro-
coeli small to large. Thyridium small, weakly impressed. Ovipositor unusu-
ally short. In the female sternite 4 often membranous medially, and subgenital
plate conspicuous and without an apical tuft of hairs. In the male the sub-
genital plate medially rounded or without a long lobe, and genital claspers not
enlarged. Apex of first tergite and propodeum often black.
Amblyteles as defined here contains only one European species, A. arma-
torius (Forster).
Three species, Amblyteles armatorius, A. camelinus and A. varipes
have been mentioned in the literature as parasitic upon the gypsy moth in
Europe. The record of A. camelinus appears erroneous. Neither camelinus
nor wavipes belong to Amblyteles. Neither of these species have been subse-
quently reared from the gypsy moth. Reared material even of A. armatorius
was not available to confirm its occurrence on the gypsy moth.
102 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
1. AMBLYTELES ARMATORIUS (Foerster) (Figs. 111, 112)
Ichneumon armatorius Forster, 1771. Novae Species Insectorum.
Centuria, 1: 82. England.
Ichneumon fasciatorius Fabricius, 1775. Systema Entomologiae, 330.
England.
Amblyteles fasciatorius: Uchida, 1930. J. Fac. Agr. Hokkaido Imp.
Univ., 25: 354. Japan. Hosts: Dendrolimus albolineatus,
Lymantria dispar, L. monacha.
Amblyteles armatorius: Townes, Momoi and Townes, 1965: 502.
Eurasia, Iran, Algeria.
This species has been reported in literature from several hosts in Japan
and Europe. Uchida (1930) apparently reported it for the first time from
Lymantria dispar in Japan. Schedl (1936) and Thompson (1946) do not list it.
This species can be readily distinguished by its black and yellow banded
abdomen and propodeum having spine-like projections on either side.
Female: Face closely punctate, punctures coalescing. Clypeus smoother
apically, its apical margin truncate or a little arcuate medially. Mandible
narrowed apically, lower tooth blunt and much shorter than the upper. Malar
space as long as the basal width of mandible. Frons and vertex closely
punctato-rugose. Occipital carina meeting hypostomal carina away from
mandibular base by a distance equal to the basal width of mandible. Thorax
rugosely sculptured. Sculpture of mesoscutum finer than that of rest of
thorax. Propodeal areola squarish to a little rectangular, almost touching
base of propodeum. Petiolar area depressed and bordered by longitudinal
carinae. Lateral projections on propodeum sharp. First tergite, particularly
postpetiole, rugose, its median field distinct and with striations. Second and
third tergites punctato-rugulose. The following tergites smoother. Gastro-
coeli short, carinate, its length about 0.5 the distance between the two. Tip
of abdomen blunt, obtuse (amblypygous).
Black, with yellow marks on body and abdomen.
Face with lateral yellow stripes along inner orbits. Flagellum brown,
tapering. Pronotal collar dorsally, hind corner of pronotum, tegula, sub-
tegular ridge, and scutellum, yellow. Legs black with extensive yellow marks
on trochanters, base, apex and a dorsal line on fore and middle femora,
whole of fore and middle tibiae, hind femur in basal 0.25 and hind tibia in
basal 0.5. All tarsi brownish, but hind tarsus darker. Abdomen black with
yellow stripes on base of second and third tergites, extending laterally, and
apex of fourth to sixth tergites. Seventh tergite broadly yellow. Sometimes
hind tibia brownish in apical half, rather than black.
Male: Sculpture similar to that of female, but color different as below.
Flagellum yellow ventrally. Scape largely yellow. Face and clypeus yellow.
Fore and middle legs almost wholly yellow except for dorsal black marks on
femora. Hind tibia yellow in basal 0.75. Second tergite yellow in basal 0.6.
Third tergite yellow except narrowly apically. Fourth and fifth wholly, and
basal half of sixth tergite black. Tip of abdomen yellow.
Length: 13-16mm. Fore wing 11-13 mm.
Specimens from Europe examined in the Townes Collections. No reared
specimens seen. Host records are given by Thompson (1957).
Distribution: Europe. Japan.
V. Gupta: Gypsy Moth Parasites 103
2. "AMBLYTELES VARIPES"” Rudow.
Amblyteles varipes Rudow, 1888. Entom. Nachr., 14: 86. 9, &.
Germany. Host: Lymantria dispar.
Amblyteles variipes: Dalla Torre, 1901-02. Catalogus Hymenopterorum,
3: 843.
Amblyteles varipes: Howard and Fiske, 1911. U. S. Dept. Agr. Bur.
Ent. Bull., 91: 85. Host: Lymantria dispar.
This species, somehow, has not been mentioned by any of the subsequent
cataloguers of gypsy moth parasites. It is also unknown to me, as no speci-
mens of it were available in the Townes Collections. Berthoumeiu (1894-96)
did not include it in his treatment of the European species. The identity of
this species is, therefore, uncertain.
A perusal of the original description reveals that it is not a true
Amblyteles and may belong to Ichneumon, Melanichneumon or Ctenichneumon.
It is characterized by having a black body, with antenna, scutellum and hind
leg wholly black. The fore and middle legs are rufous and the wings are
infumate.
The antenna is said to be serrate underneath (cf. “ Ctenichneumon), scutellum
flat, areola regularly 5-sided (cf. Ichneumon) thorax and abdomen ruguloso-
punctate and only sternites 1 and 2 withventral folds (cf. Ctenichneumon).
Length: 18 mm.
Host: Lymantria dispar.
Distribution: Germany.
3. "AMBLYTELES CAMELINUS Wesmael"
"Amblyteles camelinus Wesmael, 1844. Nouveaux Mem. Acad. Sci. Lett.
Beaux Arts Belgique, 18: 129. Belgium.
Meyer (1936) mentioned Lymantria dispar as one of the hosts of this
species. Earlier (1933, Pt 1: 304) he listed "Pergesa dispar"'as one of the
hosts in his treatment of this species. No subsequent worker has reported it
as parasitic upon the gypsy moth. This species is a parasite of the pupae of
nymphalid butterflies and the record from the gypsy moth is undoubtedly
erroneous. Perkins (1953) erected a new genus Thyrateles for the reception
of this species. Townes etal. (1965: 459) synonymized Thyrateles under
Pterocormus Foerster (= Ichneumon of authors). Kasparyan (1981: 608)
treats this species as Thyvateles camelinus Wesmael.
TRIBE PRISTICEROTINI
13. Genus COTIHERESIARCHES (Fig. 121)
Cotiheresiarches Talenga, 1929. Zool. Anz., 83: 185.
This genus is readily distinguished from the others treated here by its
petiole being flat dorsally, and wider than deep. The clypeus projects for-
ward and is triangular in outline. Mandible is strong, with only one tooth.
One species Cotiheresiarches dirus has been associated with the gypsy
moth, which is a robust looking species with a black body and yellow femora.
104 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
1. COTIHERESIARCHES DIRUS (Wesmael) (Fig. 121)
Eurylabus dirus Wesmael, 1853. Bull. Acad. Sci. Belgique, 20: 307.
Eurylabus dirus: Dalla Torre, 1901-02. Catalogus Hymenopterorum,
3: 792. Europe. Algeria. Hosts (after several authors):
Trichiura crataegi, Eriogaster lanestris, Orthosia opima.
Eurylabus dirus: Fahringer, 1922. Z. Angew. Ent., 8: 325-388. Host:
Lymantria dispar.
Cotiheresiarches dirus: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 513. synonymy.
This species was first reported as a parasite of the gypsy moth by
Fahringer (1922). Kolubayiv (in Komarek, 1937) subsequently reported it
as a moderately common parasite of the nun moth (Lymantria monacha).
There is apparently no subsequent rearing record from the gypsy moth.
It is readily distinguished from other Ichneumoningae by its petiole
flattened dorsally. This flattened area is carinate laterally. The body is
somewhat robustly built and is 14-16 mm. long. The abdomen is obtuse
apically.
Face and clypeus closely punctate. Clypeus triangular, with its apical
margin curved anteriorly and thus quite distant from the mandibles. Clypeus
and face making a concave curve. Mandible tapered apically, with its lower
tooth virtually absent. Antennal flagellum not widened medially, apically
finely long-tapered. Thorax closely punctate, punctures rough at places.
Scutellum convex and punctate. Propodeum rugose. Areola convex, com-
bined first and second lateral areas concave. Propodeal carinae irregular.
Petiole flattened dorsally, the flattened area leathery in texture and bordered
by blunt carinae. Postpetiole ruguloso-punctate, apically smoother, without
a distinct median field. Second tergite rugose medially and punctate on
either side. Gastrocoeli moderately deeply impressed, carinate. Thyridium
about as wide as the space between them. Third tergite closely finely punc-
tate. The following tergites progressively weakly punctate to mat. Abdomen
amblypygous. Female subgenital plate long and V-shaped.
Black. Fore and middle femora, tibiae and tarsi and hind femur orange-
red. Hind tibia and tarsus brownish-black, with tarsal segments apically
brown. Wings clear hyaline, stigma pale brown, veins darker, brownish-
black.
Length: 14mm. Kolubayiv (1937) mentioned the length as 15-16 mm.
Distribution: Europe.
Specimen: One female seen in the Townes Collection. No reared
material seen.
IV. SUBFAMILY MESOSTENINAE
Members of the subfamily Mesosteninae are characterized by having a
depressed abdomen, with a moderately long first tergite, with spiracles
usually behind the middle and the postpetiole widened posteriorly. Clypeus
separate from the face, often convex and its apical margin usually without
teeth. Notauli and sternaulus distinct and strongly impressed. Apical trun-
cation of scape strongly oblique. Dorsal rim of metanotum without a small
sublateral angular projection, but sometimes with such a projection just
below the hind margin, and often with a submedian pair of such projections,
V. Gupta: Gypsy Moth Parasites 105
one opposite each side of the scutellum. Propodeum with one or two trans-
verse carinae, usually the basal transverse carina alone present or more
prominent. Propodeum without longitudinal carinae except rarely. Epiplura
of second tergite narrow, often vestigeal. Tarsal claws simple. Second
recurrent vein with a single bulla, not sloping outwards, meeting subdiscoidal
vein ata right angle. Areolet usually present. Ovipositor long, without any
subapical notch, with ridges on tip of lower valve.
The subfamily Mesosteninae is the same as tribe Mesostenini in Townes
(1970). Gupta (1973) raised it to the subfamily level.
The genera that have been associated with the gypsy moth are believed to
be parasitic on the host prepupae or larvae within the cocoons. The egg is
laid externally on the body of the host larva or prepupa within the cocoon.
Emergence is from the pupa, or from the parasite's cocoon within the cocoon
of the gypsy moth.
Five species of Mesosteninae have been recorded as parasites of the
gypsy moth, viz., Cryptus cyanator Gravenhorst, C. amoenus Gravenhorst,
C. liparidis Rnd., Ischnus assertorius Gravenhorst and 'Tschnus flavus Rnd."
(Stadler, 1933). Of these, Cryptus liparidis and Ischnus flavus are nomina
nuda. They are mentioned by Rudow (not Rondani as subsequent catalogues
give), 1918, as "Cryptus liparidus Rd." and 'Ichneumon [not Ischnus| flavus
Rd. '' = nov. sp., but apparently he never described them.
Reared specimens of the other species were not available. They have not
been encountered during the surveys for gypsy moth parasites in Europe and
Asia. Their occurrence on the gypsy moth is either accidental, or more
likely, doubtful.
The nomenclature of the species is corrected according to the modern
treatment of the group. Townes, Momoi and Townes (1965), Townes (1970),
and Kasparyan (1981) may be consulted for synonymies and other taxonomic
information.
KEY TO THE GENERA AND SPECIES OF MESOSTENINAE ASSOCIATED
WITH THE GYPSY MOTH
1. Intercubitii parallel. Median portion of posterior mesosternal carina
present between the middle coxae. Sternaulus short, reaching up to
0.6 the length of mesopleurum, not sinuate. Clypeus a little arched,
weakly convex. Basal and apical transverse carinae of propodeum
equally prominent. Propodeal spiracle short, circular. First tergite
with basolateral teeth. ...... 1. Gambrus amoenus (Gravenhorst)
Intercubitii convergent towards radius. Median portion of posterior
mesosternal carina absent or indistinct. Sternaulus reaching middle
coxa and sinuate. Clypeus convex. One of the two transverse carinae
of propodeum more prominent than the other. ............ 2
2. Propodeal spiracle elongate, elliptic. Apical transverse carina of pro-
podeum strong and strongly arched medially (more prominent than the
basal transverse carina). Axillus vein strongly pigmented and diverging
from the anal margin of hind wing. Base of first tergite without a
lateral toothy or rn er. 2. Meringopus cyanator (Gravenhorst)
Propodeal spiracle short, circular. Basal transverse carina of propodeum
prominent. Apical carina weak. Axillus vein weakly pigmented and very
close and parallel to the anal margin of hind wing. Base of first tergite
106 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
with @ lateral tOoth. <6 a aes Pertanian 3. Ischnus inquisitorius
inquisitorius (Mueller)
1. Genus GAMBRUS (Fig. 74)
Gambrus Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 205: 188.
Medium sized insects. Clypeus subconvex, its apical margin convex and
with a blunt median prominence. Mesoscutum mat and with scattered punc-
tures. Apical carina of propodeum complete, its median portion more or
less bowed forwards, the lateral crests weak. Propodeal spiracle short,
circular. Areolet sub-quadrate, the intercubiti parallel. Base of first tergite
with a lateral tooth on either side. Ovipositor sheath 1.0-2.0 as long as hind
tibia. Hind tibia without a basal whitish band.
Gambrus is a Holarctic genus with species extending into the northern
parts of the Oriental Region. It is related to Agrothereutes and Aritranis and
the characters of the three genera merge in some taxa. The above descrip-
tion will identify the genus and further details can be found in Townes (1970)
treatment of the genera of Agrothereutina.
One species, Gambrus amoenus, was listed by Howard and Fiske (1911)
as a parasite of the gypsy moth in Europe.
1. GAMBRUS AMOENUS (Gravenhorst) (Fig. 76)
Cryptus amoenus Gravenhorst, 1829. Ichneumonologia Europaea, 2: 623.
(Cryptus) Avitranis amoenus: Howard and Fiske, 1911. U. S. Dept.
Agr. Bur. Ent. Bull., 91: 85. Host: Lymantria dispar.
This species has been referred to as Cryptus amoenus, Aritranis amoenus
or Spilocryptus amoenus in the literature on the gypsy moth parasites. |
Howard and Fiske (1911) first reported it as a parasite of Lymantria dispar,
based upon information in their card file. Thompson (1946: 449) cites
Stadler (1933) and Schedl (1936) as his source of information about its being
parasitic upon the gypsy moth.
The American species Gambrus nuncius (Say) is a junior synonym of
Gambrus amoenus (n. syn.), which has been reared from Callosamia
angulifera, Callosamia promethi, C. angulifera, Samia cynthia, Antheraea
polyphemus, Acronicta sp., and Battus philenor. According to Townes and
Townes (1962) the normal hosts are Callosamia species. The parasite over-
winters as a cocoon in the host cocoon and the adult emerges in the following
spring. Its occurrence on the gypsy moth is doubtful or accidental.
Face closely finely punctate on a granular surface. Clypeus subconvex
and shiny, with scattered punctures. Malar space mat, about equal to the
basal width of clypeus. Occipital carina coming to the base of mandible and
meeting the hypostomal carina near it, or a little erased at that place. Frons
centrally rugoso-striate. Vertex granulose. Interocellar distance 0.85 as
long as ocellocular distance. Upper part of temple mat, as wide as the width
of eye in profile. Lower temple polished. Mesoscutum mat, with scattered
shallow punctures. Scutellum subconvex, with scattered punctures on a
smooth surface. Side of thorax rugoso-punctate, with metapleurum becoming
finely reticulate. Propodeum convex, smoother basally, longitudinally striate
V. Gupta: Gypsy Moth Parasites 107
medially between the basal and apical transverse carinae, both of which are
prominent, and rugose apicad of the apical transverse carina. First tergite
smooth, second mat with scattered punctures, third finely mat and rather
closely shallowly punctate and the following tergites progressively subpolished.
Ovipositor about 0.66 to 0.70 the length of abdomen. Upper valve of oviposi-
tor tip compressed, in profile view convex.
Black. Mandible medially red. Clypeus medially and scape may be red
marked. Antenna brownish-black with flagellar segments 5-9 white, and seg-
ments 4 and 10 partly white. Tegula brownish-yellow in European specimen
and black in American series. Legs yellowish-brown with fore coxa partly
brownish and apices of hind femur and tibia blackish. Hind tibia often later-
ally also fuscous. Hind tarsus white. Basal three abdominal tergites orange-
brown. Fourth and the following tergites black with apices of sixth and
seventh tergites and often also the fifth, white.
Male: Propodeum with a faint indication of anareola. Tyloids on seven
flagellar segments. Tyloids linear with the median tyloids a little widened
and rounded above. Hind coxa black. Abdominal tergites 2, 3 and part of 4
orange-brown, rest black. Seventh tergite with a white triangular mark.
Rest as in the female.
Length 9-11 mm. Fore wing 5-9 mm. Ovipositor 3-4 mm.
Specimens from Europe (Germany) and U.S.A. examined, but no reared
specimens seen. It may be that all European specimens have been from
cocoons imported from North America, and that the species is native only to
North America.
Townes and Townes (1962) provided a key to the North American species.
Schaffner and Griswold (1934) give biological information on this species.
2. Genus MERINGOPUS (Fig. 77)
Meringopus Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 186.
For the taxonomy of the genus, refer to Van Rossem (1969).
Medium sized insects. Clypeus strongly convex, its apical margin trun-
cate. Malar space 0.8 to 1.2 the basal width of mandible. Mandibular teeth
equal. Flagellum normal, not flattened or enlarged. Mesoscutum with smooth
lateral areas, punctures sparser than on other parts. Notauli moderately
deep, reaching beyond center of mesoscutum. Epomia, sternaulus and pre-
pectal carina complete and distinct. Propodeal spiracle 2.8 to 4.0 as long
as wide. Apical transverse carina of propodeum complete, forming weak
lateral crests. Areolet pentagonal, large, the intercubiti convergent anteri-
orly. Axillary vein of hind wing strong and diverging from the anal margin.
First tergite stout, without basolateral teeth. Postpetiole flat and wide, its
dorsal and lateral carinae distinct. Second tergite mat, with weak sparse
punctures to subpolished. Abdomen mat. Ovipositor tip short to elongate,
with a nodus. |
This genus is separated from other ischnine genera by the presence of
clearly visible tentorial pits on the frons. Buathra also has conspicuous
tentorial pits on the frons, but in Buathra the axillus vein in the hind wing is
converging towards the anal margin and is usually weakly pigmented.
There are several species in Eurasia and North America. The Eurasian
species were revised by Van Rossem (1969).
One species, Meringopus cyanator was listed by Howard and Fiske (1911)
108 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
as a parasite of the gypsy moth. No earlier reference could be traced.
2. MERINGOPUS CYANATOR (Gravenhorst) (Figs. 78, 79)
Cryptus cyanator Gravenhorst, 1829. Ichneumonologia Europaea, 2: 442.
Cryptus cyanator: Howard and Fiske, 1911. U.S. Dept. Agr. Bur. Ent.
Bull.,91: 85. Host: Lymantria dispar.
Meringopus cyanator: Van Rossem, 1969. Tijdschr. v. Ent., 112: 188.
Trachysphyrus cyanator: Griffiths, 1976. Parasites and predators of the
gypsy moth: A Review, p. 42.
Body with long brownish pilosity. Face convex medially, with a promin-
ance below antennal sockets, closely punctate, punctures superimposed ona
granular surface. Malar space granulose, 1.1 as long as the basal width of
mandible. Clypeus convex, with scattered punctures on a polished surface.
Frons rugose, antennal scrobes smooth, concave with tentorial pits usually
well developed (sometimes weak). Vertex punctate. Temple in profile as
wide as eye, punctate, the punctures sparser below, the interspaces shiny.
Interocellar distance 0.87 as great as ocellocular distance. Occipital carina
abruptly erased at a distance equal to the basal width of mandible and not
joining hypostomal carina. Thorax strongly rugose. Mesoscutum with
polished areas in between irregularly placed punctures. Epomia complete
to upper margin of pronotum. Propodeum with apical transverse carina
forming weak lateral crests and with an irregularly and weakly formed
areola. Central area of propodeum a little convex and narrowed, followed by
a longer and steep slope to the apex. Axillary vein in hind wing strongly
pigmented and diverging from inner hind margin of the wing. Legs with
femora and tibiae normal, not dilated or flattened respectively. Abdomen
granulose. Ovipositor tip normal, teeth on lower valve not strong ventrally,
nor flanged out or projecting when seen in profile.
Black. Palpi brown to black. Mandible reddish medially. Antennae
brownish-black. Outer orbits with faint reddish lines. A reddish spot on
vertex close to eye. Thorax black. Subtegular ridge narrowly reddish.
Wings infumated. All coxae and trochanters black, femora reddish-brown,
tibiae reddish brown basally and fuscous apically and dorsolaterally, tarsi
largely fuscous. Abdomen blackish-brown with a faint violet iridescence.
Apical margins of basal 1 or 2 tergites show faint brownish coloration.
This species is rather close to Meringopus nigerrimus murorum (Tschek)
from Scandinavia and the Alps, but the latter species has well developed
ventral ridges on the ovipositor tip.
Length: 12-8-15.7 mm. Fore wing 8.8-11.2 mm. Ovipositor 4.5-5.5
mm.
Distribution: Europe: Germany, Netherlands, Poland, Denmark,
Russia.
Hosts: Lymantria dispar, Panolis flammea, Malacosoma neustria,
Diloba coeruleocephala, and Phragmatobia fuliginosa.
3. Genus ISCHNUS (Fig. 75)
Ischnus Gravenhorst, 1829. Ichneumonologia Europaea, 1: 638.
V. Gupta: Gypsy Moth Parasites 109
Body usually slender. Clypeus small, convex and often pyramidal in
profile, its apical margin convex. Mesoscutum mat and with minute punctures.
Notaulus extending beyond center of mesoscutum. Sternaulus long and sinu-
ate. Propodeal spiracle circular. Apical propodeal carina variable (in the
species discussed here weak and broadly interrupted medially, almost indis-
tinct). Areolet pentagonal, intercubiti convergent towards the radial vein.
Axillus vein weakly pigmented and very close to the anal margin, its tip
turned towards the margin. Base of first tergite with a lateral tooth on
either side. First tergite slender, subpolished. Abdomen finely mat. Ovi-
positor about 0.5 the length of abdomen.
Ischnus assertorius Gravenhorst was apparently first listed by Rudow
(1917) as a parasite of the gypsy moth. The present day name of it is
Ischnus inquisitorius inquisitorius (Mueller). Townes and Townes (1962)
recognized six subspecies of inquisitorius: two from Europe, one from
Northern Japan, and three from North America. They have also provided a
key to separate them.
3. ISCHNUS INQUISITORIUS INQUISITORIUS (Mueller) (Fig. 75)
Ichneumon inquisitorius Mueller, 1776. Zool. Danicae Prodromus,
p. 151.
Ichneumon assertorius Fabricius, 1793. Entomologia Systematica, 2: 140.
Ischnus assertorius: Rudow, 1917. Ent. Ztschr. Frankfurt, 31: 67.
Hosts: Lymantria dispar, Xestia triangulum.
Face granuloso-punctate. Frons rugose. Clypeus smoother, convex.
Vertex granulose, Malar space granulose, about equal to basal width of
mandible. Introcellar distance a little less than ocellocular distance (8: 10).
Temple and vertex behind lateral ocelli receding, the vertex rather abruptly
so. Mesoscutum mat, with fine punctures. Thorax generally otherwise
closely punctate, tending to be rugose at places. Propodeum rugulose, its
apical transverse carina weak and absent in the central area, laterally form-
ing weak crests. First tergite slender and subpolished, rest of the tergites
mat. Ovipositor about half the length of abdomen, its tip finely tapered.
Black, with abdomen reddish-brown. Marks along inner orbits extending
on vertical orbits, a mark between and behind lateral ocelli, a mark on the
center of clypeus, anterior and upper margins of pronotum dorsally, its
hind corner, subtegular ridge, scutellum apically and metascutellum, yellow.
Tegula brownish-black. All coxae and trochanters, black. Legs otherwise
reddish-brown, with apices of hind femur and tibia fuscous and hind tarsus a
little dark-brown. Tip of abdomen black. Male darker, particularly the
abdomen brown. Yellow on head more extensive. Male sometimes also has
yellow marks on side of thorax and on propodeum.
Length: 8-10 mm. Fore wing 5-7 mm. Ovipositor 3-4 mm.
Distribution: Eurasia. Other subspecies occur in Japan and North
America.
Hosts: Lymantria dispar, Pandemis cerasana, Archips rosana
(Kasparyan, 1981). Xestia triangulum (Rudow, 1917).
According to Townes and Townes (1962) this species is related to the
Japanese Ischnus assimilis Uchida and Ischnus yezoensis Uchida.
110 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
V. SUBFAMILY TRYPHONINAE
Members of the tribe Tryphoninae are small to large sized ichneumon-
flies that are ectoparasitic on lepidopterous caterpillars and on sawfly larvae.
They are characterized by having a medium-sized to large transverse clypeus
with its apical margin usually broad and beset with a fringe of long parallel
hairs. Male flagellum devoid of tyloids. Sternaulus absent or short. Pro-
podeum usually partly to completely areolated. Sometimes (as in Netelia)
propodeal carinae reduced or absent. Tarsal claws usually pectinate.
Areolet usually present, pointed or petiolate above. Second recurrent vein
usually with two bullae. Nervellus intercepted variously. First tergite with
a glymma, its spiracles before the middle. Abdomen depressed or in Netelia
compressed and slender. Ovipositor usually short, sometimes long, its tip
without a subapical dorsal notch and usually without conspicuous teeth.
This subfamily contains several tribes, but only one genus (Netelia) of
the tribe Phytodietini is associated with the gypsy moth. The tribe Phytodi-
etini contains two genera Phytodietus and Netelia, which are external para-
sites of lepidopterous larvae. They are characterized by having two spurs
on hind tibia, propodeum without carinae or with only sublateral crests and
with transverse striations, prepectal carina present, and nervellus vertical
or reclivous. The genus Nefelia has twisted mandibles, long slender
brownish colored body, and a compressed and long abdomen.
1. Genus NETELIA (Figs. 68, 133)
Paniscus of authors, not of Schrank.
Netelia Gray, 1860. Ann. Mag. Nat. Hist., (3) 5: 341.
Body long, slender, with fore wing 6 to 23 mm. long. Mandibles twisted,
the lower tooth much smaller than the upper. Eye and ocelli enlarged.
Eyes emarginate opposite antennal sockets. Basal 0.65+ of propodeum with —
transverse striations, usually with a pair of transverse crests. Nervellus
intercepted above the middle. Ovipositor 1.0 to 2.0 as long as the apical
depth of abdomen, its tip sharp and slender.
General body coloration brownish or ferrugineous, sometimes with a
few blackish marks.
Members of the genus Nefelia are external parasites of exposed lepidop-
terous larvae. Several subgenera are recognized (Townes, 1969: 149), but
the two species reported from the gypsy moth belong to the subgenus Nefelia,
which has normally pectinate hind tarsal claws, occipital carina complete,
nervulus distad of basal vein, lateral carina of scutellum reaching to its apex,
and thorax usually without definte yellow markings.
Two species of Netelia—as 'Paniscus cephalotes Holmgren" and "'P,
testaceus Gravenhorst" were reported by Ritihl (1914) as parasites of Lyman-
tria dispar in Europe. They have since been mentioned by Wolf and Kraube
(1922), Meyer (1931) and Thompson (1946) in the gypsy moth literature. I
have not come across any rearing records, nor have I seen any reared speci-
mens of them. Both these species are only occasional parasites of the gypsy
moth, if they attack it at all. These two species have often been misidentified
in the past; so their true identities are uncertain.
The correct name of "Paniscus cephalotes"' is Netelia (Netelia) vinulae
V. Gupta: Gypsy Moth Parasites 111
(Scopoli). The identity of 'Paniscus testaceus"' cannot be established and is
referred here as Nefelia sp.
1. NETELIA (NETELIA) VINULAE (Scopoli) Figs. 69-73, 133)
Ichneumon vinulae Scopoli, 1763. Entomologia carniolica. .., p. 286.
Paniscus cephalotes Holmgren, 1858, Svenska. Vetensk Akad. Handl.
(NPs 2 (806 She
Taxonomy: Ruhl, 1914: 26. Townes, Momoi and Townes, 1965: 95.
Delrio, 1975: 64. Kaur and Jonathan, 1979: 137.
Female: Head wider than long. Face convex medially and moderately
closely punctate. Malar space 0.2 as long as the basal width of mandible.
Frons transrugulose. Temple strongly convex, as wide as eye. Occipital
carina rather weak and ending shortly before the oral carina. Pronotum,
mesoscutum and scutellum finely closely punctate. Mesopleurum moderately
punctate and subpolished. Metapleurum and propodeum finely closely
striated. Lateral crests of propodeum prominent. Hind tarsal claw strongly
bent apically and with about 14 rather fine pectines and 2 ungual bristles.
Tibial bristles moderate. Nervulus distad of basal vein by 0.3-0.4 its length
and distinctly bent in its upper 0.4. Areolet rather small, oblique, sub-
sessile. First tergite stout and swollen, about 3.5 as long as wide at apex.
Male genitalia: Gonoforceps large and exserted, without a apico-dorsal
spine. Brace broad, moderately long and supporting a large U-shaped pad
apically. Penis valve normally shaped.
Color: Brown. Ocellar triangle lightly infuscate. Stigma yellow.
Length: 2: 17-19mm. Fore wing 13.5 to15 mm. ©: 13-22 mm.
Distribution: Europe, China, India, Japan, Russia.
Hosts: It is apparently a polyphagous parasite of various common
lepidopterous pests of forest trees, including Lymantria dispar and L. mon-
acha (Kaun and Jonathan, 1979). As no reared specimens could be seen, its
occurrence on the gypsy moth could not be confirmed.
The above description is adapted from Kaur and Jonathan (1979), who
examined the lectotype of N. cephalotes. The type of N. vinulae no longer
exists.
2. NETELIA (NETELIA) sp.
Paniscus testaceus Gravenhorst: Ruhl, 1914. Soc. Ent., 29 (5): 26.
Host: Lymantria dispar. Europe.
Ruhl (1914) reported Paniscus testaceus Gravenhorst as a parasite of
Lymantria dispar, which record has been repeated in literature. However,
no reared specimens are at hand to confirm the identity of the species involved.
Nor have any subsequent rearing records been discovered in the literature.
The identity of N. testaceus is very doubtful and the type is also lost.
This species has often been misidentified in the past. Delrio (1974) who
revised the western Palaearctic species of Netelia, listed it as "species
incerte sedis", mentioning that it is a composite species. Meyer (1936)
apparently confused it with Netelia melanurus (Thomson) when he reported
melanurus as a parasite of the gypsy moth in 1936, but not in his taxonomic
112 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
treatment of melanurus in 1935.
Netelia melanurus is a rather distinct species with a black abdominal tip.
Since what Ruhl referred to as festaceus is uncertain, the record from the
gypsy moth is referred here as Netelia (Netelia) sp.
Townes, Momoi and Townes (1965) and Delrio (1974) provide further in-
formation on Palaearctic Netelia species and their hosts.
VI. SUBFAMILY BANCHINAE
The subfamily Banchinae includes moderately long, stout or slender
insects with fore wing 1.8 to 16 mm. long. Clypeus small, wide or narrow,
usually separated from face by an epistomal groove, its apical margin round,
notched or truncate, without an apical fringe ofhairs. Mandibular teeth equal
to subequal, the upper sometimes broad to obliquely truncate. Male flagellum
without tyloids. Sternaulus absent or short. Postpectal carina absent. Pro-
podeum with apical transverse carina evenly arched and usually strong. Tar-
sal claws usually pectinate. Areolet present or absent. Nervellus inter-
cepted variously. First abdominal segment stout to slender, its spiracles
before the middle, or at middle, its dorsolateral carinae usually absent.
First sternite not fused with its tergite. Glymma nearly always present.
Abdomen depressed, its apex often compressed. Female subgenital plate
large, prominent, its apex with a median notch. Ovipositor with a subapical
notch, without a node, the lower valve without teeth. Ovipositor and its
sheaths long to short. :
Members of the subfamily Banchinae are usually internal parasites of
lepidopterous larvae. Oviposition is usually within the young larvae.
Emergence of the adult parasite is from a cocoon spun after the parasite
larva has killed and left its host.
Only one genus Banchus has been associated with the gypsy moth. Keys to
separate it from other genera and tribes of Banchinae are given by Townes
(1970).
1. Genus BANCHUS Fabricius (Figs. 80, 137, 138)
Banchus Fabricius, 1798. Supplementum Entomologiae Systematicae,
p. 209, 233.’
For synonymical references refer to Townes (1970). Townes and Townes
(1978) treated the Nearctic species. Chandra and Gupta (1977) treated the
Oriental species. Aubert (1978) gives a catalog and host records of the
Palaearctic species.
Body moderately stout. Face broad above, weakly narrowed toward lower
side. Apical margin of clypeus with a median notch. Upper tooth of mandible
wider and longer than the lower tooth and its apex with a weak concavity.
Malar space 0.5 to 0.8 the basal width of mandible. Eye emarginate near
antennal socket. Fourth segment of maxillary palpus nearly always expanded
apically, the expansion faint to strong and more expanded in the male. Occi-
pital carina entire or interrupted medially above, joining hypostomal carina
above base of mandible. Prepectal carina absent. Apex of scutellum usually
with a median point or spine. Propodeum short, its apical transverse carina
complete or erased medially. Propodeal spiracle long, elliptic. Areolet
V. Gupta: Gypsy Moth Parasites 113
usually large, receiving second recurrent vein near the middle. Nervulus
distad of basal vein by 0.2 to 0.6 its length. Nervellus intercepted far above
the middle. Abdomen apically compressed. First tergite without dorsal or
dorsolateral carinae. Epipleura of tergites 2 and 3 about 0.7 as wide as long.
Ovipositor very short, its sheaths about 0.13 as long as hind tibia.
Two species of Banchus are reported in literature as parasites of the gypsy
moth, viz., Banchus femoralis Thomson = hasiator (Fabricius) and B. falcator
Fabricius = falcatorius (Fabricius). The record of the latter species was
apparently based upon guess work. None of these species have turned up in
subsequent rearings and no voucher specimens are available to confirm their
association with the gypsy moth.
KEY TO THE SPECIES OF BANCHUS ASSOCIATED WITH THE GYPSY MOTH
Apex of scutellum with a median spine. Abdominal tergites black, sub-
polished. Inner orbits yellow (broadly so in male). Hind femur black-
Leb Se mee 4 5 OD Oe eee Se 1. hastator (Fabricius)
Apex of scutellum with a median point, without a conspicuous spine.
Abdominal tergite 2 with a broad reddish-brown band (sometimes apex of
tergite and base of tergite 3 also reddish-brown). In males tergites
1-3 largely yellowish-brown. Inner orbits in female black and in male
largely yellow. Hind femur yellowish-brown or yellow in male.
Europe. Doubtful, almost certainly erroneous record.
2. falcatorius (Fabricius)
1. BANCHUS HASTATOR (Fabricius) (Fig. 137)
Ichneumon hastator Fabricius, 1793. Entomologia Systematica, 2: 167.
Europe.
Banchus femoralis Thomson, 1897. Opuscula Entomologica, 22: 2411.
Sweden. Syn. by Fitton, 1978.
Banchus femoralis: Kolubayiv, 1934. Acta Ent. Soc. Ent. Csl., 31: 114.
Czechoslovakia. Host: Lymantria dispar.
Kolubajiv (1934) apparently reared it from the gypsy moth for the first
time in Czechoslovakia. No subsequent rearing record has been seen.
Female: Face punctate. Clypeus, inner orbits, frons and vertex, mat
with frons a little rough and dull. Frons excavated and with circular striations
just above antennal sockets. Malar space 0.7 to 0.8 as long as the basal width
of mandible. Interocellar distance 1.2 as long as the ocellocular distance.
Tip of flagellum tapered, narrowed and cylindrical. Mesoscutum, mesopleurum
and metapleurum punctate, punctures on mesoscutum closer than those on
mesopleurum and metapleurum. Scutellum shiny, with minute scattered punc-
tures, its apex with a pointed spine, about 0.25 as long as the length of scu-
tellum. Scutellum with erect hairs surrounding the spine. Propodeum
leathery, ruguloso-punctate in basal half and rugose to a little rugose striate
in apical half. Its apical transverse carina weak and irregularly represented.
Propodeal spiracle long, linear. Abdomen polished, with shallow scattered
and minute punctures on basal three tergites. First tergite flat dorsally,
without dorsal carinae, a little depressed apicad of the projecting spiracles.
Ovipositor short, its sheaths hardly exerted, more or less parallel-sided,
114 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
wider and truncate apically.
Black. Face broadly along inner orbits and narrowly along outer orbits,
clypeus, scape ventrally, tegula, fore femur on the anterior aspect, fore
tibia largely, middle femur dorsally, and middle tibia except apically, and
all second trochanters, yellow. Tegula often and apex of scutellum surround-
ing the spine, brownish to brownish-yellow. Fore and middle femora with
black marks. Fore and middle tibiae and tarsi brownish at places. Hind leg
largely black or blackish-brown, with apex of femur, basal 0.6 of tibia and
base of basitarsus, yellowish-brown. All coxae and first trochanters black.
Metapleurum often with a yellow oval spot. Abdomen with brownish or yellow-
ish brown apical margins on tergites 1-3. Basal 2-3 sternites often apically
broadly yellow.
Male: Similar to the female in sculpture and coloration, except for the
following sexual differences:
Tip of flagellum somewhat attenuate and flattened. Flag setae on flagellar
segments not visible (may be present, but small). Fourth segment of maxil-
lary palpus flattened and widened apically. Face largely yellow with only a
broad central black stripe. Scutellar spine short. Oval yellow spot on meta-
pleurum absent. Abdominal tergites black. Male claspers with a concave
lower margin, tapered apically (appear beak-like).
Length: 11-13 mm. Fore wing 8.5 to 10mm. Ovipositor 0.5 mm.
Specimens: Several males and females from Europe examined in Townes
Collection. No reared specimen seen.
Distribution: Europe.
Hosts: Lymantria dispar, Panolis flammea, Zeiphera diniana (= griseana.
Hb.) and Diprion sp. (after Thompson, 1957).
2. BANCHUS FALCATORIUS (Fabricius)
Ichneumon falcatorius Fabricius, 1775. Systema Entomologiae, p. 332.
Denmark.
Banchus falcatorius: Fabricius, 1798. Suppl. Ent. Syst., p. 234.
Banchus falcator Fabricius: Morley, 1915. Revision of Ichneumonidae
in British Museum, 4: 138. Germany. Syn., hosts. [Doubtful
association with the gypsy moth.].
This species was first reported as a parasite of Lymantria dispar by
Morley (1915), which has been cited by Aubert (1978). Morley's record was
based on a male specimen from Germany, bearing the following data, "Between
Wilmannsdorf and Schwangendorf, 6 PM, under willows, also flying. Larva of
L. dispar (gypsy moth) common." It is clear that the host association was
simply by guess-work.
Since there is no definite evidence of the association of B. falcatorius with
the gypsy moth, and since it has not been reared from that host subsequently,
this species is to be removed from the list of ichneumonid parasites associated
with the gypsy moth.
V. Gupta: Gypsy Moth Parasites 115
VIl. SUBFAMILY CREMASTINAE
Members of the subfamily Cremastinae are long slender insects with fore
wings 2.5 to 14 mm. long. Abdomen strongly compressed. Eyes bare.
Ocelli of male sometimes enlarged. Clypeus small to large, separated from
face by an epistomal groove, its apical margin convex. Mandible short, bi-
dentate. Sternaulus absent. Prepectal carina present. Postpectal carina
complete. Propodeum usually completely areolated, with longitudinal as well
as transverse carinae. Spurs of all tibiae set ina membranous area that is
separated from the membranous area of tarsal insertion by a sclerotized
bridge (not seen in other ichneumonids). Tarsal claws partly to completely
pectinate. Epipleurum of third tergite not separated or only partly separated
from its tergite. Female subgenital plate unspecialized, usually not visible.
Ovipositor long, with a subapical dorsal notch.
Members of the subfamily Cremastinae are internal parasites of lepidop-
terous larvae living in concealed situations. Some of them also attack cole-
opterous larvae, or larvae in exposed situations, like the gypsy moth. Emer-
gence of the parasite is from the mature larva about to pupate.
Only one genus and species, Pristomerus vulnerator (Panzer) has been
associated with the gypsy moth in Eurasia and North Africa.
1. Genus PRISTOMERUS Curtis (Fig. 81)
Pristomerus Curtis, 1836. British Entomology, 13: 624.
For full synonymical references and relationships with other cremastine
genera, refer to Townes (1971). This genus is easily distinguished from all
other genera treated in this paper by. having a tooth on the lower side of hind
femur and ovipositor tip sinuate.
Body moderately slender. Abdomen moderately to strongly compressed
apically. Occipital carina usually complete. Lateral carina of scutellum
absent, or present only basally. Hind femur often swollen and with a ventral
tooth followed by a series of minute teeth, especially in male. Stigma wide.
Radial cell short. Areolet absent. Nervellus intercepted near its lower 0.35.
First tergite moderately slender, usually longitudinally carinate. Lower
edges of first sternite nearly parallel-sided, not touching each other. Thyridi-
um on second tergite transverse or subcircular, near base of the tergite.
Epipleurum of second tergite narrow, separated by a crease, and turned under.
Apex of male clasper rounded. Ovipositor long, only a little shorter than
fore wing, its tip sinuate.
1. PRISTOMERUS VULNERATOR (Panzer) (Fig. 81)
Ichneumon vulnerator Panzer, 1799. Faune Insectorum Germanicae,
Heft 72, pl. 5. Europe.
Pristomerus vulnerator: Curtis, 1836. British Entomology, 3: 624.
England.
Pristomerus vulnerator: Barsacq, 1913. Rev. Phytopath. Appl. Paris,
1(5): 70-73. France. Host: Lymantria dispar.
116 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Pristomerus vulnerator: Mokrzecki, 1913. Reports [of the Chief
Entomologist to the Zemstov] on Injurious Insects and Diseases of
Plants in Govt. of Taurida during the year 1912. Simferopol, 1913,
p. 1-23. Host: Lymantria dispar.
For fuller synonymical references, hosts and distributional records,
refer to Townes, Momoi and Townes (1965).
Barsacq (1913) and Mokrzecki (1913) first reported it parasitic in young
caterpillars of gypsy moth in France and Taurida (Russia) respectively.
Meyer (1927) reported having reared it in Russia. Obrtel (1949) and Sedivy
(1970) gave an extensive host range for this species.
Female: Face punctate, granuloso-punctate along inner orbits. Clypeus
smooth. Width of face almost equal to the length of face and clypeus. Malar
space about 0.7 the basal width of mandible, punctate. Temple and vertex
posteriorly strongly receding from the eye. Temple 0.25 the width of eye.
Vertex concave above. Occipital carina close to the lateral ocelli, distant
from the ocelli by about the ocellar diameter or slightly more than that.
Vertex and frons (excluding the antennal scrobes), closely finely granulose.
Interocellar distance equal to the ocellocular distance. Mesoscutum
granuloso-punctate, punctures set ona granular surface. Scutellum flat,
punctate, subpolished in between punctures. Mesopleurum punctate, inter-
Spaces equal to at least the diameter of the punctures and shiny. Metapleurum
somewhat coarsely punctate. Pleural area punctate, with interspaces equal to
the diameter of the punctures and shiny. Propodeal spiracles situated at or
a little below the middle of the spiracular carina (pleural part of basal trans-
verse carina). Propodeum convex, shallowly to moderately punctate. Areola
smoother and petiolar area usually transrugose. Propodeal areolation com-
plete. Areola broad, 1.5 times as long as its maximum width at costula.
Costula arising at basal 0.33 to 0.4 of the length of areola. Apical closing
carina of areola often weak in the middle. Hind coxa strongly granulose.
Hind femur with one strong tooth in apical 0.33, followed by a series of min-
ute teeth between it and apex. First and second tergites longitudinally striate.
The following tergites subpolished and compressed. Ovipositor long, its
sheath 0.66 as long as the fore wing, its tip sinuate.
Male: Eyes strongly diverging ventrally. Vertex constricted. Ocelli
large and raised. Ocellocular space almost obliterated. Propodeal carinae
strong. Areola a little longer and narrowed apically and basally, widest at
costula. Costula arising from basal 0.6 of areola. Pleural area of propode-
um and metapleurum somewhat sparsely punctate and subpolished, sometimes
a little strongly and irregularly so. Otherwise similar to the female.
Black. Head devoid of brownish orbital marks. Mandible, tegula, and
fore and middle legs except their coxae, yellow. Scape and pedicel black to
brownish-black. Coxae black. Fore coxa may be partly brown. Hind leg
brownish-yellow with black marks on trochanter, femur, and apex of tibia
and tarsus except basally. The extent of black on hind leg variable. Abdomen
black either wholly or apices of tergites brownish-yellow, or apical tergites
largely yellowish-brown.
In males third tergite usually partly to wholly yellowish-brown. Some-
times faint brownish lines seen along inner orbits.
Length: 6-7 mm. Fore wing 4 to 4.5mm. Ovipositor 4 mm.
Distribution: Eurasia, China, Japan, Korea.
Hosts: Lymantria dispay and many other common lepidopterous pests
[see Meyer (1927), Obrtel (1949) and Sedivy (1970)].
V. Gupta: Gypsy Moth Parasites 117
Pristomerus vulnerator appears to be a variable species occurring in
Eurasia. It is closely related to Pristomerus orbitalis Holmgren and the two
have often been mixed up in European literature. P. orbitalis has a wider
face, wider than high, wider temples, ocellocular distance greater than inter-
ocellar distance, vertex not strongly concave behind, occipital carina con-
siderably away from lateral ocelli, in males lateral ocelli distinctly separated
from eye margin, mesoscutum punctate, without granulations, propodeum
smoother, propodeal areola narrow and elongate, about 4.0 as long as wide,
and propodeal spiracle usually above the middle on the spiracular carina. The
hind coxa is minutely punctate, not densely granulose as in P. vulnerator,
The head is with yellowish-brown orbital stripes encircling the eyes.
VIII. SUBFAMILY ANOMALINAE
The subfamily Anomalinae is characterized by having a coarsely reticulate
propodeum, anda long, slender and strongly compressed abdomen. Clypeus
often not separated from face by a groove, its apex often with a median point.
Occipital carina often at the outer margin of head. Head quadrate. Mandible
bidentate. Epomia usually long. Sternaulus absent. Propodeum reticulate
wrinkled, without carinae, its apex often produced beyond bases of coxae.
Areolet absent. Legs long, slender. First tergite slender, long, without a
glymma, its tergite and sternite fused, and spiracle behind the middle. Ab-
domen strongly compressed. Ovipositor and its sheaths short. Ovipositor
with a subapical dorsal notch.
Members of the subfamily Anomalinae are internal parasites of the larvae
of Lepidoptera, except that the genus Anomalon is reported from Coleoptera.
The emergence is from the pupa. The parasite larva spins a flimsy cocoon
within the pupae of Lepidoptera. The larval morphology is similar to that of
the Metopiinae. |
Rudow (1911) reported two species of "Anomalon" from Lymantria dispar
as well as L. monacha, viz., Anomalon flaveolatum Gravenhorst and
A, pallidium Gravenhorst. The former species now belongs to Agrypon while
the latter to Barylypa. Why no subsequent cataloger has listed these species
as gypsy moth parasites, is unknown to me. Kirchner (1856) reported
Anomalon (Trichomma) enecator Rossi as a parasite of Lymantria dispar.
Morley (1915) stated that Gaulle (1908) bred it from Lymantria dispar in France.
Kovacevic (1925) reported Barylypa perspicillator Gravenhorst as a parasite of
the gypsy moth in Yugoslavia. This name is a junior synonym of B. delictor
(Thunberg). None of these parasites have been confirmed as gypsy moth para-
sites by subsequent rearings, nor have I seen any reared specimens of them.
KEY TO THE GENERA OF ANOMALINAE ASSOCIATED WITH
THE GYPSY MOTH
1. Eye surface hairy. Inner margins of eyes strongly convergent toward
mandible. Ovipositor sheath 2.0 to 3.8 as long as the apical depth of
abdomen. Discoidella and often also the brachiella veins absent.
1. Trichomma (Trichomella)
Kye surface bare. Inner margins of eyes weakly convergent, or parallel.
Ovipositor sheath less than 2.0 the apical depth of abdomen. .... 2
118 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
2. Discoidella present. Frons with a median vertical carina. Postnervulus
intercepted near upper 0.25. . 2... 0 ee ee ee co oe 2. Barylypa
Discoidella absent. Frons without a median vertical carina. Postnervulus
intercepted near upper 0.38. ......s6sseeseeeoe-s 3. Agrypon
1. Genus TRICHOMMA (Fig. 84)
Trichomma Wesmael, 1849. Bull. Acad. Roy. Sci. Lett. Beaux-Arts
Belgique, 16(2): 119, 139.
Trichomella Szépligeti, 1910. Notes Leyden Mus., 32: 91.
Inner eye margins moderately to very strongly convergent ventrad. Eyes
with long dense hairs. Frons without a median carina or tooth, often with
transverse wrinkles. Apex of clypeus convex or subtriangular, with a median
tooth that varies from very small to large. Temple narrow. Occipital carina
complete, close to ocelli and reaching base of mandible, separate from hypos-
tomal carina. Lower tooth of mandible a little shorter than the upper. Flagel-
lum moderately long, lower front corner of pronotum truncate. Epomia pre-
sent. Scutellum flat to convex, carinate laterally. Prepectal carina extending
to 0.9 the height of mesopleurum. Sternaulus absent. Posterior mesosternal
carina interrupted in front of each middle coxa. Propodeum and metapleurum
reticulate. Apex of propodeum extending up to 0.5 the length of hind coxa.
Tarsal claws pectinate on basal half or more. Middle tibia with two spurs.
Nervulus a little distad of basal vein. Intercubitus basad of second recurrent
vein. Discoidella and brachiella veins present of absent. Postnervulus meet-
ing discocubital cell before its middle. Second tergite much longer than the
third. Epipleurum of third tergite not separated by a crease. Ovipositor 2.0
to 3.8 as long as the apical depth of abdomen.
Species of Tvichomma are generally parasites of the larvae of Microlepi-
doptera, particularly those which are concealed in rolled leaves, mining in
soft plant tissues, etc. Oviposition is into the host larva and the adult emerges
from the host pupa by biting off the entire anterior end of the puparium. Tvi-
chomma enecator (Rossi) was, however, reported as a parasite of Lymantria
dispar by Kirchner (1856).
1. TRICHOMMA (TRICHOMELLA) ENECATOR (Rossi) (Fig. 85, 86)
Ichneumon Enecator Rossi, 1790. Fauna Etrusca, 2: 48. Italy.
Anomalon (Trichomma) enecator: Kirchner, 1856. Lotos, 6: 150.
Czechoslovakia. Host: Lymantria dispar.
Trichomma (Trichomella) enecator: Townes, Momoi and Townes, 1965.
Mem. Amer. Ent. Inst., 5: 362.
This species was first reported as a parasite of Lymantria dispar (= Bom-
bax dispar) by Kirchner (1856) from Czechoslovakia. According to Morley
(1915) it is a parasite of a number of tortricid hosts in England, but was also
bred from the pupae of Lymantria dispar by de Gaulle in France. It is listed
as a parasite of Lymantria dispar in Europe by several subsequent cataloguers,
like Wolf and Kraube (1922), Meyer (1931), Stadler (1933), Schedl (1936), and
Thompson (1946), etc.
Female: Face a little convex, minutely punctate as well as polished.
V. Gupta: Gypsy Moth Parasites 119
Clypeus polished, pointed apically. Frons rugoso-striate. Malar space 0.2
the basal width of mandible. Interocellar distance 1.1 the ocellocular distance.
Mesoscutum rugoso-punctate. Scutellum shallowly rugose, flat dorsally and
strongly carinate laterally. Upper 0.3 of pronotum polished and a little swollen
medially with widely spaced parallel and strong carinae. Mesopleurum trans-
carinate, carinae somewhat weaker centrally and interspaces punctate. Meta-
pleurum and propodeum reticulate, with honey-comb like cells. Hind wing
with distal abscissa of cubitella, discoidella and brachiella virtually absent.
Petiole slender, circular in cross-section. Postpetiole a little swollen.
Tergite 2, 1.75 as long as the third. Third and the following tergites strongly
compressed laterally and their epipleurae not separated from the tergites by a
crease. Ovipositor long, slender, about 3.2 to 3.5 as long as the apical depth
of abdomen, and 0.75 as long as the fore wing.
Black. Face, clypeus, mandible, palpi, outer orbital border narrowly,
upper margin of pronotum (narrowly to broadly), scutellum centrally, often
fore and middle legs largely, and hind trochanters yellow. Postpetiole, hind
femur, basal half of hind tibia and whole of tarsi, and ventrolateral aspects of
abdominal tergites, yellowish-brown. Hind coxa, trochanter, base of femur,
and apical 0.3 to 0.6 of tibia often brown (extent of brown variable). Base of
hind tibia often brown.
Length 10-11 mm. Fore wing 5.5 to6.0 mm. Ovipositor 4.0-4.5 mm.
Specimens: Several females seen in the Townes Collections from Europe,
but no specimens reared from the gypsy moth are at hand.
Hosts: Lymantria dispar. Several other hosts are listed by Gauld and
Mitchell (1977) and Kasparyan (1981), but not the gypsy moth.
Distribution: Eurasia. Japan.
2. Genus BARYLYPA Foerster (Fig. 87)
Barylypa Foerster, 1869. Verh. Naturh. Ver. Rheinlande, 25: 156.
Inner eye margins weakly convergent ventrad. Eye surface hairless.
Frons with a median vertical carina. Apex of clypeus pointed medially.
Occipital carina complete, close to posterior ocelli, joining hypostomal carina
at or immediately before mandibular base. Lower mandibular tooth about 0.6
as long on the upper. Antenna moderately long, that of female without a white
band. Clypeus usually with a median apical tooth. Scutellum short, weakly
convex and usually with lateral carina. Lower anterior margin of pronotum
without a tooth, lower corner truncate. Epomia running along pronotal collar,
not deflected above. Middle tibia with two spurs. Tarsal claws pectinate up to
middle. Intercubitus basad of second recurrent vein. Postnervulus intercepted
near upper 0.25. Discoidella present. Tergite 2 much longer than tergite 3,
its epipleurum separated by a crease. Abdomen apically strongly compressed,
with epipleura of tergite 3 onwards not separated by a crease. Ovipositor
about 2.0 or long as apical depth of abdomen.
Two species of Barylypa are reported in literature as parasites of the gypsy
moth, viz., B. delictor (Thunberg) and B. pallida (Gravenhorst).
120 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
1. BARYLYPA DELICTOR (Thunberg) (Fig. 88, 89)
Ichneumon delictor Thunberg, 1822. Mém. Acad. Imp. Sci. St. Péters-
bourg, 8: 265; 1824, Ibid, 9: 319. Sweden.
Barylypa delictor: Roman, 1912. Zool. Bidr. Fran Uppsala, 1: 249.
Barylypa perspicillator Gravenhorst: Kovacevic, 1925. Sumar List.,
49(1): 1-5. Yugoslavia. Host: Lymantria dispar.
Barylypa perspicillator (Gravenhorst) was first reported from the gypsy
moth by Kovacevic (1925). Meyer (1935) synonymized perspicillatoy under
delictor (Thunberg).
This species is unknown to me. No specimens could be examined. Kas-
paryan (1981) gives a key to the Eurasian species.
Distribution: Eurasia. J
Hosts: Several hosts are mentioned by Meyer (1931-36), Sedivy (1957) and
Kasparyan (1981), including Lymantria dispar.
2. BARYLYPA PALLIDA (Gravenhorst)
Anomalon pallidum Gravenhorst, 1829. Ichneumonologia Europaea,
3: 675. Rudow, 1911. Internat. Ent. Ztschr., 5:99. Host:
Lymantria dispar.
Barylypa pallida: Schmiedeknecht, 1908. Opuscula Ichneumonologica,
19: 1507.
This species was first reported from the gypsy moth by Rudow (1911) but
has not been listed subsequently by Schedl or Thompson. Kasparyan (1981)
provides a key to distinguish it from other Eurasian species. He also lists
B. humeralis Brauns as a synonym of it. It is unknown to me.
3. Genus AGRYPON Foerster (Fig. 90)
Agrypon Foerster, 1860. Verh. Naturh. Ver. Rheinlande, 17: 151.
This genus is rather similar to Barylypa and the main differences appear to
be the absence of discoidella vein in the hind wing, frons without a vertical
carina, and the epomia with a different course. The postnervulus is inter-
cepted near upper 0.38, and not very high as in Barylypa. Other characters
are mostly similar (cf. Townes, 1971, pp 144 and 139). Townes also provides
fuller synonymical references.
4. AGRYPON FLAVEOLATUM (Gravenhorst) (Fig. 90)
Ophion flaveolatum Gravenhorst, 1807. Vergl. Uebers. Zool. Syst.,
p. 268.
Anomatlon flaveolatum: Rudow, 1911. Internat. Ent. Ztschr., 5: 99.
Europe. Hosts: Lymantria dispar, L. monacha,
Agrypon flaveolatum: Townes, Momoi and Townes, 1965. Mem. Amer.
Ent. Inst., 5: 373.
V. Gupta: Gypsy Moth Parasites 121
This has not been reported subsequently from the gypsy moth. It occurs in
Europe, China, Japan and Korea. Kasparyan (1981) gives some diagnostic
characters and a long list of hosts, but not the gypsy moth. Schmiedeknecht
(1908) gave a description of it.
IX. SUBFAMILY OPHIONINAE
Members of the subfamily Ophioninae are characterized by having a
slender, long, and compressed abdomen with the first tergite long, tubular and
its spiracles placed far behind the middle. Ocelli very large. Clypeus separ-
ated from the face by a groove. Tarsal claws pectinate. Epomia absent.
Second brachial cell with a long spurious vein, that parallels its hind margin.
Areolet absent, the intercubitus far distad of the second recurrent vein. Ovi-
positor short and with a subapical dorsal notch, without any ridges on the lower
valve.
They are medium to large sized species with longer wings. The body color
is usually pale brown. Adults are generally crepuscular or nocturnal.
Members of the subfamily Ophioninae are world wide in distribution. They
are endoparasites of medium to large sized lepidopterous larvae.
Only two genera, Ophion and Enicospilus have been associated with the
gypsy moth, by one species of each genus. Rearing records are scanty. There
are no recent records and no reared material was available for study. Even the
identities of the species of the genera Ophion and Enicospilus are subject to
doubt (Gauld, 1976, 1978) and Gauld and Mitchell (1978, 1981).
KEY TO THE GENERA OF OPHIONINAE ASSOCIATED WITH THE
GYPSY MOTH
1. Posterior transverse carina of mesosternum broadly interrupted in front
of each middle coxa. Mandibles normal, teeth in the same plane and
equal. Fore wing without a glabrous area (fenestra)... . 1. Ophion
Posterior transverse carina of mesosternum complete or rarely incom-
plete. Mandibles strongly narrowed and twisted apically, teeth subequal.
Fore wing with a fenestra, often with one or more sclerites present.
2. Enicospilus
1. Genus OPHION (Fig. 82)
Ophion Fabricius, 1798. Suppl. Ent. Syst., p. 210, 235.
Townes (1971) provides synonymical references and a key to the world
genera of Ophioninae. Gauld (1976, 1978) gives information on the British
and some European species.
Body long and slender. Color reddish-brown, sometimes with pale stripes
on mesoscutum. Fore wing 8 to 21 mm. long. Ocelli large, the lateral ones
almost touching the eye. Antenna long, slender, longer than the length of the
fore wing. Mandible not narrowed, nor twisted apically, teeth equal or nearly
equal. Notauli generally sharply impressed in anterior 0.3 to 0.4. Scutellum
moderately convex, usually without lateral or with short lateral carinae.
Posterior transverse carina of mesosternum present only as lateral rudiments.
122 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Propodeum partly to completely areolated, or rarely without carinae. Fore
wing with pterostigma rather stout. Areolet absent. Discocubital cell without
a fenestra, but with a small hairless area below the base of stigma. Fore
tibial spur with a membranous flange behind the macrotrichial comb.
Only one species, Ophion luteus (Linnaeus) is mentioned in literature as a
parasite of the gypsy moth.
1. "OPHION LUTEUS (Linnaeus)"'
Ichneumon luteus Linnaeus, 1758. Systema Naturae, (Ed. 10),1: 566.
Ophion luteus: Townes, Momoi and Townes, 1965. Mem. Amer. Ent.
Inst., 5: 317. Synonymical references and distribution. Holarctic.
Kolomiyetz (1958) reported having reared this species from gypsy moth
pupae in Siberia in July 1954. It was considered as a rare parasite. This is
apparently the first record of an Ophion species from Lymantria dispar. It
has, however, been previously reported several times as a parasite of
Lymantria monacha.
Gauld (1976, 1978) mentioned that Ophion luteus (Linnaeus) has been a
commonly misidentified species. According to him Ophion luteus of authors is
Ophion slaviceki (Kriechbaumer). He (1978) provided a key to distinguish the
two and the others occurring in Britain.
Which one of the above mentioned two species was actually reared by
Kolomiyetz cannot be ascertained without the specimens. The following table
will distinguish the two:
Ophion luteus Ophion slavickei
Outer tibial spur of middle leg : Outer tibial spur of middle leg
less than 0.8 as long as the fourth 0.8 or more as long as the fourth
tarsal segment. Smaller species, tarsal segment. Larger species,
fore wing 13-15 mm. long. fore wing 15-18 mm. long.
Characters in common of these two species are: Propodeum with trans-
verse carinae. Malar space less than 0.5 the basal width of mandible. First
subdiscoidal cell unevenly hairy. Ocelli a little away from the eye. Antenna
with less than 64 segments. Middle tibial spurs unequal in length.
Brown. Interocellar area and propodeum entirely orange-brown to
yellowish. Wings slightly yellow-tinged. Thorax uniformly brown, never pale
marked except rarely on mesepimeron.
Distribution: Europe.
2. Genus ENICOSPILUS (Figs. 83, 139)
Enicospilus Stephens, 1835. Illustrations of British Entomology,
Mandibulata, 7: 126.
some of the recent studies on the genus are of Townes (1971), and Gauld and
Mitchell (1978, 1981).
Body slender. Abdomen long and strongly pone fea: Antenna long.
Eyes and ocelli large. Malar space short. Mandible wide at base and strongly
V. Gupta: Gypsy Moth Parasites 123
narrowed and somewhat twisted before the middle, its upper tooth longer than
the lower. Notauli indistinct. Scutellum usually long, its lateral carina
reaching to apex or to near apex. Posterior mesosternal carina usually com-
plete. Propodeum with basal carina present or rarely obsolete, without other
carinae except that oblique or longitudinal wrinkles may be present apically.
Pterostigma rather narrow. Areolet absent. Discocubital cell with a small to
large glabrous area (fenestra), usually containing 1, 2 or several corneous
scleromes. Fore tibial spur without a membranous flange, with only an anten-
nal brush of closely spaced hairs.
General body color pale brown to reddish-brown with abdominal tip often
black marked.
Only one species, Enicospilus merdarius (Gravenhorst) has been mentioned
in literature as parasitic on the gypsy moth. The earlist record could be
traced back only to Ruhl (1914). There is no recent rearing record confirming
its association with the gypsy moth.
Gauld and Mitchell (1981) mention Enicospilus transversus Chiu as a para-
site of Lymantria sp. from Bangalore, India.
2. ENICOSPILUS MERDARIUS (Gravenhorst) (Fig. 83)
Ophion merdarius Gravenhorst, 1829. Ichneumonologia Europaea, 3: 698.
Enicospilus merdarius: Stephens, 1835. Illustrations of British Ento-
mology, Mandibulata, 7: 311.
This species occurs in Europe. It has often been misidentified in literature
and does not occur in the Orient (Gauld and Mitchell, 1981). In the absence of
reared specimens it is difficult to ascertain if it is really a parasite of the
gypsy moth.
Face finely punctate. Clypeus convex, smoother, its apical margin almost
smooth and impressed. Upper tooth of mandible about 2.0 as long as the lower.
Frons, vertex and temple smoother, subpolished. Interocellar distance about
2.0 the ocellocular distance. Occipital carina complete. Mesoscutum very
minutely punctate and subpolished. Scutellum elongate, slightly convex and
minutely punctate, its lateral carina strong and reaching apex of scutellum.
Mesopleurum finely punctate, its central area often striato-punctate. Pre-
pectal carina arched toward anterior margin of mesopleurum but not touching
it. Metapleurum punctate to rugoso-punctate. Propodeum smooth basad of
basal transverse carina, circularly reticulo-striate in the depressed area
covering petiolar region. Disco-cubital cell with two scleromes in the fenes-
tra, the distal sclerome not distinct, the proximal sclerome pear-shaped, and
the central sclerite rounded-oval but its inner side toward quadra irregular
and unpigmented. Wings moderately densely hairy. Abdomen strongly com-
pressed, with first tergite tubular. Second and the following tergites with
dense short hairs. Thyridium elongate, separated from base of second ter-
gite by about 2.5 to 3.0 its length. Ovipositor short, not longer than the apical
depth of abdomen, pointed apically.
Reddish-brown, with orbits, face, frons and clypeus, largely yellowish.
Tip of abdomen not black. Sometimes apical segments ventrally a little darker.
Length: 20-24mm. Fore wing 14-16 mm. Ovipositor 3 mm.
Specimens from various localities in Europe examined in the Townes Col-
lection. No reared material was available.
Hosts: Lymantria dispar (vide Ruhl, 1914). Kasparyan (1981) lists only
124 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Panolis flammea as its host. Wolff and Krausse (1922), and Meyer (1935)
mentioned it from the gypsy moth in Germany and Russia respectively.
Stadler, Schedl and Thompson also listed it as such.
This species is very similar to, if not the same as the North American
Enicospilus purgatus (Say).
X. SUBFAMILY XORIDINAE
Members of the subfamily Xoridinae are parasitic upon wood boring Cole-
optera and therefore all records from Lymantria are erroneous.
Rudow (1911) listed two species from the gypsy moth, viz., Xylonomus
irrigatoy Fabr., and Xorides praecatorius Fabr. Both belong to Xorides.
They are not parasitic upon the gypsy moth. They are therefore removed from
the list of gypsy moth parasites.
Another species, Odontomerus dentipes Gmelin was recorded by Morley
(1908: 11) from Lymantria monacha. Morley's record was from an erroneous
reporting of Ratzeburg (1844).
XI. SUBFAMILY SCOLOBATINAE
l. OPHELTES GLAUCOPTERUS (Linnaeus)
Members of this genus are parasitic upon Cimbex (saw flies) and not on
Lepidoptera. The record of its occurrence on Lymantria dispar, originating
from Ruhl (1914) is erroneous. This species is therefore to be removed from
the list of parasites of the gypsy moth.
Gyorfi (1963) mentioned having reared it from the gypsy moth in Hungary.
Evidently there was some mix up either in the hosts reared, or in the deter-
minations.
REFERENCES
Anonymous. Exotic parasites of Lymantria dispar established in Pennsylvania and
unestablished exotic parasites. Pennsylvania Dept. Environmental Resources
Bureau of Forest Pest Management, Report, 3p.
Aubert, J.F. 1969. Les Ichneumonides ouest-paléarctiques et leurs hotés. 1.
Pimplinae, Xoridinae, Acaenitinae. Ouvrage Publée avecle Concours du
CNRS. 304 p.
Aubert, J.F. 1975. Ichneumonides pétiolées inédities avec un genre nouveau.
Bull. Soc. Ent. Mulhouse. Oct.-Dec. 1974: 53-60.
Aubert, J.F. 1978. Les Ichneumonides ouest-paléarctiques et leurs hétes 2.
Banchinae et suppl. aux Pimplinae. OPIDA, 318 p.
Barsacq, J. 1918. Les Bombyx dissemblabe ou spongieuse Lymantria (Ocneria)
dispar L. Rev. Phytopath. Appliqué, Paris 1 (5): 70-73.
Beeson, C. F.C. and Chatterjee, S.N. 1935. On the biology of the Ichneumonidae
(Hymenoptera). Indian Forest Res. (N.S.) Ent. 1 (8): 151-168.
Berthoumieu, G.V. 1894-96. Ichneumonides d’Europe et des pays limitrophes.
Ann. Ent. Soc. France, 63: 241-274, 505-664 (1894); 64: 213-296, 553-564
(1895); 65: 285-418. Suppl. 393-399 (1896).
V. Gupta: Gypsy Moth Parasites 125
Bouché, P.F. 1833. Naturgeschiste der Schadlichen aus nutzlichen Garten-Insekten
und die bewarhtesten Mittel zur Verteilung der ersten. Berlin, Nicolai, 176p.
Britton, W.E. 1935. The gypsy moth. Conn. Agri. Exptl. Sta. Bull. 375: 623-647.
Burgess, A. F. and Crossman, S8.S. 1929. Imported insect enemies of the gypsy
moth and brown tail moth. U. S. Dept. Agri. Tech. Bull. 86: 1-148.
Campbell, R.W. 1963. Some ichneumonid sarcophagid interactions in the gypsy
moth (Porthetria dispar L.) (Lepidoptera: Lymantriidae). Canad. Ent. 95:337-
343.
Carlson, R. W. 1979. Family Ichneumonidae. In Krombein et al.: Catalog of
Hymenoptera in America north of Mexico, 1: 315-740.
Cecconi, G. 1924. Manuale di Entomologia Forestale. Padua.
Chandra, G. and Gupta, V.K. 1977. Ichneumonologia Orientalis, Part VII.
The tribes Lissonotini and Banchini (Hymenoptera: Ichneumonidae: Banchinae).
Oriental Insects Monographs 7: 1-291.
Dalla Torre, C.G. de 1901-1902. Catalogus Hymenopterorum hucusque descrip-
torum systematicus et synonymicus, Vol. 3, 1141p.
Delrio, G. 1975. Revision des especies ouest-paléarctiques du Genere Netelia
Gray (Hym., Ichneumonidae). Studi Sassar. Sez. UI-Annalia Della Facolta
di Agraria dell’Universita di Sassari, 23: 1-126.
Doane, C.C. and McManus, M. (Editors) 1981. The Gypsy Moth: Research toward
integrated pest management. U.S. Dept. Agriculture Forest Service, Tech.
Bull. No. 1584: 757 p.
Drea, J.J. 1978. A resumé of recent studies made by the European Parasite Labor-
atory with Lymantria dispar L. and its natural enemies in Europe, Iran, and
Japan. [Plant Protection] Zastita Bilja, Beograd 29: 119-125.
Drea, J.J. and Fuester, R.W. 1979. Larval and pupal parasites of Lymantria dispar
and notes on parasites of other Lymantriidae (Lep.) in Poland, 1975.
Entomophaga 24: 319-327.
Dysart, R.J. 1982. Personal communication.
Fernald, C.H. 1892. The gypsy moth. Mass. Hatch Exp. Sta. Bull. 19: 109p.
Fitton, M.G. 1978. In Kloet and Hincks. A check-list of British Insects. 2nd
Edition. Handbooks of identification of British Insects. Vol. 11 (4, Hymen-
optera), 1-159 (Ichneumonidae p. 12-45). Roy. Ent. Soc. London.
Forbush, E.H. and Fernald, C.H. 1896. The gypsy moth. Wright and Porter
Printing Co., State Printers, Boston. 495 p.
Fukaya, S. 1936. On the Hymenopterous parasites of Lymantria dispar (L.)
(In Japanese). Oyo Dobutsugaku Zasshi 8: 232-335.
Fukaya, S. 1950. (In Yasumatsu and Watanabe, 1964). Not seen.
Fusco, R.A. and Simons, E.E. 1973. (Revised, 1977). A review of some common
eypsy moth adult parasites and predators in Pennsylvania. PartI. Native
and established species. Dept. of Environmental Resources, Bureau of
Forestry, Div. of Forest Pest Management, Pennsylvania, 13 p.
Gauld, I.D. 1976. Notes on British Ophioninae (Hym., Ichneumonidae). Part 3.
Ent, Gaz. ore iia-1i7..
126 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1963
Gauld, I.D. 1978. Notes on British Ophioninae (Hymenoptera, Ichneumonidae).
Part 4. Ent. Gaz. 29: 145-149.
Gauld, I. D. and Mitchell, P.A. 1978. The taxonomy, distribution, and host pre-
ferences of African parasitic wasps of the subfamily Ophioninae. 287 p.
Commonwealth Inst. Entomology. London.
Gauld, I.D. and Mitchell, P.A. 1981. The taxonomy, distribution and host pre-
ferences of Indo-Papuan parasitic wasps of the subfamily Ophioninae (Hymen-
optera: Ichneumonidae). 611 p. Commonwealth Inst. Entomology, London.
Gaulle, J.de 1908. Catalogue systematique et biologique des hyménoptéres de
France. Feuille Jeun. Natural. 38: 64-66, 77-82, 102-104, 120-122, 140-141,
183-184, 209-210. 234-235, 252-257.
Gravenhorst, J.L.C. 1829. Ichneumonologia Europaea. Vratislaviae, Vol. 1, 830 p.
Vol, 2) 989 p. Vol. 3, 1097 p.
Griffiths, K. J. 1976. The parasites and predators of the gypsy moth: A review of
the world literature with special application to Canada. Dept. Environ. Canad.
Forest Service, Ontario, Report 0-X-243. 92 p.
Griffiths, K.J. 1980. A bibliography of gypsy moth literature. Vols. 1 and 2.
Canadian Forestry Service, Sault Ste. Marie. Report 0-X-312.
Gupta, V.K. 1962. Taxonomy, zoogeography, and evolution of Indo-Australian
Theronia (Hymenoptera: Ichneumonidae). Pacific Ins. Monogr. 4: 1-142.
Gupta, V.K. 1975. Ichneumonological Explorations in India, Delhi. 126 p.
Gupta, V.K. and Maheshwary, S. 1977. Ichneumonologia Orientalis, Part IV.
The tribe Porizontini (Campoplegini) (Hymenoptera: Ichneumonidae). Oriental
Insects Monogr. 5: 1-267.
Gyo6rfi, J. 1963. A Lymantria dispar L. parazitai. Kulonl. Allattani Kozlem
1963: 50-53.
Hedlund, R.C. and Mihalache, G. 1980. Parasites recovered from pupae of
Lymantria dispar (Lep.: Lymantriidae) in Romania, 1978. Entomophaga
25: 55-59.
Heinrich, G.H. 1937. A list and some notes on the synonymy of the types of the
subfamily Ichneumoninae Ashmead (Hymenoptera) in the collections of the
British Museum and Hope Dept. of the Oxford University Museum. Ann. Mag.
Nat. Hist. (10) 20: 257-279.
Heinrich, G.H. 1960-62. Synopsis of Nearctic Ichneumonidae Stenopneusticae with
particular reference to the northeastern region (Hymenoptera). Parts I-VI.
Canad. Ent. 92 (Suppl. 15): 1-87; 92 (Suppl. 18): 91-205; 93 (Suppl. 21):
209-368; (Suppl. 23): 371-505; (Suppl. 26): 511-671; (Suppl. 27): 27: 677-802;
(Suppl. 29): 29: 807-886.
Heinrich, G.H. 1968. Burmesische Ichneumoninae 4 & 5. Ent. Tidskr. 89: 77-106;
197-228.
Heinrich, G.H. 1978. Eastern Palearctic Ichneumoninae (In Russian). Acad. Sci.
USSR 80 p.
Herard, F. and Fraval, A. 1980. La repartition de les enemies naturelles de
Lymantria dispar (L.) (Lep.:Lymantriidae) au Maroc, 1973-1975. Acta
Oecologia 1 (1): 35-48.
V. Gupta: Gypsy Moth Parasites 127
Herard, F., Mercadier, G., and Abai, M. 1979. Situation de Lymantria dispar
(Lep.: Lymantriidae) et de son complexe parasitaire en Iran en 1976.
Entomophaga 24: 371-384.
Hinz, R. 1964. Uber einige Typen der Holmgrenschen Gattung Limneria (Hym. Ich.
Ophioninae). Entomaephaga 9: 67-73.
Horstmann, K. 1969 (1968). Bemerkungen uber die Typusarten von vier Gattungen
der Ichneumonidae (Hymenoptera. Opusc. Zool. 102: 1-4.
Horstmann, K. 1974 (1973). Ubersicht uber die europaeischen Arten der Gattung
Venturia Schrottky (Hymenoptera, Ichneumonidae). Mitt. Deutsch. Ent. Ges.
ert ~12.
Hoy, M.A. 1976. Establishment of gypsy moth parasitoids in North America: An
evaluation of possible reasons for establishment or non-establishment. In
Perspectives in Forest Entomology. Academic Press. p. 215-232.
Howard, L.O. and Fiske, W. F. 1911. The importation into the United States of the
parasites of the gypsy moth and the brown tail moth. U. S. Dept. Agr. Bur.
Ent. Bull. 91: 1-344,
Kamiya, K. 1934. Studies on the morphology, bionomics, and hymenopterous para-
Sites of the pine caterpillar (Dendrolimus spectabilis Butl.) (In Japanese).
Bull. Forest Expt. Sta. Govt. -Gen. Chosen, Korea 18: 1-110.
Kamijo, K. 1962. Natural enemies parasitic on moths attacking poplar. (In
Japanese). Rept. Koshunai Forest Tree Breeding Station 1: 83-90.
Kovacevic, Z. 1925. Parasites of Malacosoma neustria L. and Porthetria dispar L.
(In Czech). Sumar List 49: 1-5.
Kasparyan, D.R. 1973. A review of the Palearctic ichneumonids of the tribe
Pimplinae (Hymenoptera, Ichneumonidae). The genera Itoplectis Forst. and
Apechthis Forst. Ent. Rev. 52: 444-450.
Kasparyan, D.R. 1974. Review of the Palearctic species of the tribe Pimplini
(Hymenoptera, Ichneumonidae). The genus Pimpla Fabricius. Ent. Review
53 (2): 102-117.
Kasparyan, D.R. 1981. Fauna Hymenoptera USSR. Ichneumonidae (In Russian).
Vol, 3; .687 0.
Kaur, R. and Jonathan, K.J. 1979. Ichneumonologia Orientalis, Part VII. The
Tribe Phytodietini from India (Hymenoptera: Ichneumonidae). Oriental Insects
Monograph 9: 1-276.
Kirchner, L. 1856. Die von mir erzogenen ichneumonen der Umgegend von Kaptilz.
Lotos 6: 107-158.
Kolomietz, N.G. 1958. Parasites of harmful insects in Siberia (English translation).
Ent. Rev. 37: 522-534.
Kolubajiv, S. 1934. The results of breeding parasites from their hosts in the State
Experiment Institute in Prague in 1929-33. (In Czech). Acta Soc. Ent. Csl.
$1: 59-68, 119-120, 155-1638,
Kolubajiv, S. 1937. Parasitenverzeichnis und Bestimmungstabelle. In Komarek:
Kritisches vort ueber die Beduntung der Insekten parasiten der Nonne.
Z. Angew. Ent. 24: 95-117,
128 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Kolubajiv, S. 1937. Notes on the biology of the nun moth and its chief insect para-
sites (In Czech). Lesn. Pr. 16: 169-199.
Krombein, K.V. etal. 1979. Catalog of Hymenoptera in America north of Mexico.
Vols. 1-3. Smithsonian Institution Press, Washington.
Leraut, Patrice 1980. Liste systématique et synonymique des Lépidoptéres de
France, Belgique, et Corse. Suppl. 4 Alexanor et au Bull. Soc. Ent. France
334 p.
Marsh, P.M. 1979. The braconid (Hymenoptera) parasites of the gypsy moth,
Lymantria dispar (Lepidoptera: Lymantriidae). Ann. Ent. Soc. America
72: 794-810.
Matsumura, S. 1931. 6000 illustrated insects of Japan Empire [p. 61].
Meyer, N.F. 1927 and 1929. Schlupfwespen die in Russland in den Jahren 1881-1926
aus Schaedlingen gezogen sind. Izv. Otdj. Prikladn. Ent. Gossund. Inst.
Agron. 3: 78-91; 4: 251-246.
Meyer, N.F. 1931. Parasitic insects from harmful rural pests of gardening and
forestry. (In Russian). p. 98-110.
Meyer, N.F. 1933-1936. Parasititscheskije perepontschatokrylyje sem.
Ichneumonidae SSSR i sopredetnych stran. Tables systematiques des
hyménoptéres parasites (fam. Ichneumonidae) de 1’7URSS et des pays limi-
trophes. Inst. Zool. Acad. Sci. URSS 1933, 1: 1-458; 1933, 2-325; 1934,
3: 1-271; 1935, 4: 1-535; 1936, 5: 1-340; 1936, 6: 1-356.
Mocsdary, A. (S.) 1885. Data ad cognitionem Ichneumonidum Hungariae I.
Ichneumones Wesm. [1844]. Magy. Tud. Acad. Math. es Termeszettud
Kozlem. 20: 591-144.
Mocsary, A. (S.) 1878. Data ad faunam Hymenopterologicum Sibiricae. Tijdschr.
v. Ent. 21: 198- 200.
Mokrzecki, S.A. 1913. Reports [of the Chief Entomologist to the Zemstov] on
injurious insects and diseases of plants in Govt. of Tauridia during the year
1912 (In Russian). Simferopol 1913, 231 p.
Momoi, S. 1961. On some host known Ichneumon flies from Japan, with descrip-
tions of a new species (Hymenoptera: Ichneumonidae). Kontyu 29: 271-272.
Momoi, 8. 1963. New host records of Ichneumonidae of Japan and new homonymy.
Insecta Matsumurana 26: 54.
Momoi, S. 1970. Ichneumonidae (Hymenoptera) of the Ryukyu Archipelago. Pacific
Insects 12: 327-399.
Morley, C. 1903-1915. Ichneumonologia Britanica. The Ichneumons of Great
Britain, Parts 1-5. London.
Morley, C. and Rait-Smith, W. 1933. The hymenopterous parasites of the British
Lepidoptera. Trans. Roy. Ent. Soc. London, 81: 133-183.
Mosher, F.H. 1915. Food plants of the gypsy moth in America. U. 8S. Dept. Agri.
Bull. 250, 39 p.
Muesebeck, C.F.W. and Dohanian, 8. M. 1927. A study in hyperparasitism with
particular reference to the parasites of Apanteles melanoscelus (Ratzeburg).
U. S. Dept.Agri. Bull. 1487, 35p.
V. Gupta: Gypsy Moth Parasites 129
Muesebeck, C.F.W. and Parker, D.L. 1933. Hyposoter disparis Viereck, an
introduced ichneumon parasite of the gypsy moth. J. Agri. Res. 46: 335-347.
Oehlke, J. 1967. Westpali#arktischen Ichneumonidae I. Ephialtinae. In Junk:
Hymenopterorum Catalogus (nova editio), Part 2: 1-48.
Oehlke, J. and Townes, Henry K. 1969. Schmiedeknechts Ichneumonidentypen aus
der Kollektion des Museums Rudolstadt (Hymenoptera: Ichneumonidae). Beitr.
z. Ent. 19: (3-4): 395-412.
Orbtel, R. 1949. K. otrzce druhu rodu Pristomerus Curtis [Notes on species of the
genus Pristomerus Curtis] (Hym.: Ich.). Ent. Listy (Folia Ent.) 12: 102-106.
Perkins, J. F. 1953. Notes on British Ichneumoninae with descriptions of new
species. Bull. Brit. Mus. (Nat. Hist.) Ent. 3: 105-176.
Perkins, J. F. 1959-60. Handbooks for the identification of British insects.
Hymenoptera, Ichneumonoidea, Ichneumoninae, I and II. Vol. 7, part 2 (ai
and aii). Roy. Ent. Soc. London. 116 and 213 p.
Picard, F. 1921. Le Bombyx disparate ou spongieuse (Lymantria dispar). Progres
Agri. Vitic. 76 (33): 160-165.
Pschorn-Walcher, H. 1974. Gypsy moth (Porthetria dispar): Work in Europe in 1974.
Annual Project Statement. Commonw. Inst. Biol. Control. Delemont,
Switzerland (Unpublished report).
Rao, V.P. 1967 (1966). Survey for natural enemies of gypsy moth. July 25, 1961 to
July 24, 1966. Final Technical Report. Commonw. Inst. Biol. Control
Indian Station. 50p.
Rao, V.P. 1972. Evaluation of hymenopterous parasites of the gypsy moth and study
of the behavior of the promising species. Final Technical Report. March 1,
1967 to August 31, 1972. Commonw. Inst. Biol. Control Indian Station 25 p.
Rasnitsyn, A.P. 1981. Gravenhorst’s and Berthoumieu’s types of Ichneumonidae
Stenopneusticae preserved in Wrociaw and Cracow, Poland (Hymenoptera,
Ichneumonidae). Polskie Pismo Ent. 51: 101-145.
Ratzeburg, J.T.C. 1844. Die Ichneumonen der Forstinsecten in forstlicher und
entomologischer Bezeichung. Ein Anhang zur Abbildung und Beschreibung der
Forstinsecten. Vol. 1, 224p.
Ratzeburg, J.T.C. 1852. Ibidem. Vol. 3, 272p.
Riley, C.V. and Howard, L.O. eds. 1894. Work on the gypsy moth in 1893. Insect
Life. U.S. Dept. Agri. Div. Ent. Period. Bull. 6: 338-339.
Romanyk, N. 1965. The study of parasites, predators, and diseases of the gypsy
moth (Lymantria dispar) and the possibility of their application in the biological
control. Final Technical Report. Buln. Serv. Plagas. For. 65 p.
Rondani, C. 1871-1872. Degli insetti parassiti e delle loro vittime. Bull. Soc. Ent.
Ital. 1871, 3: 121-143, 217-243; 1872, 4: 41-78, 229-259, 321-342.
Rondani, C. 1873. Degli insetti novici e dei loro parassitti. Bull. Soc. Ent. Ital.
5: 38-30,
Rudow, F. 1911. Dei Schmarotzer der deutschen Spinner. Bombycidae. Internat.
Ent. Ztschr., 5: 90-91, 98-99, 118-119.
Rudow, F. 1917a. Die Ichneumonidengattung Amblyteles und ihre Wirte. Ent.
Ztschr. Frankfurt 31: 25-26, 31, 33-35.
130 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
-Rudow, F. 1917b. Ichneumoniden und ihre Wirte. Ent. Ztschr. Frankfurt. 31: 58-59,
61-62, 66, 76, 71-72.
Rudow, F. 1918-1919. Ichneumon. Ent. Ztschr. Frankfurt. 32: 59, 63-64, 71-72,
75, (1918); 79-80, 8&4, 88 (1919).
Ritihl, M. 1911. Liste neuerdings beschriebener oder gezogener Parasiten und ihre
Wirte. Soc. Ent. 26: 31-40.
Riihl, M. 1914. Liste neuerdings beschreibener oder gezogener Parasiten und ihre
Wirte. Soc. Ent. 29 (5): 26-30.
Schaefer, P.W. (1981-1982). Personal communication.
Schaffner, J.V. and Griswold, C.L. 1934. Macrolepidoptera and their parasites
reared from field collections in the northeastern part of the United States.
Misc. Publ. U. S. Dept. Agri. No. 188, 160p.
Schedl, K.E. 1936. Der Schwammspinner (Porthetria dispar L.) in Euroasien,
Afrika, und Neuengland. Monogr. Angew. Ent. 12: 1-242.
Schmiedeknecht, O. 1908-1911. Opuscula ichneumonologica, vol. 4, Ophioninae.
pp. 1407-2271.
Sedivy, J. 1957 (1956). A contribution to the knowledge of the ichneumon flies of the
tribes Hellwigiini, Anomalonini, and Therionini in Czechoslovakia (Hym:
Ichneumonidae) (In Czech). Acta Fauna Ent. Mus. Natl. Praha 1: 127-139.
Sedivy, J. 1963. Faunistische und taxonomische Bemerkungen zu den Ichneumoniden
der Tschechoslowakei, Pimplinae, IT (Hymenoptera: Ichneumonidae ,
Pimplinae). Acta Fauna Ent. Mus. Natl. Praha 9: 155-177.
Sedivy, J. 1970. Westpalaearktische Arten der Gattungen Dimophora, Pristomerus,
Eucremastus, and Cremastus (Hym., Ichneumonidae). Acta Sci. Nat. Brno
4 (11): 1-38.
Seyrig, A. 1927. Etudes sur les Ichneumonides, II (Hymen.). Eos 3: 201-242.
Shapiro, V.A 1956. The principal parasites of Porthetria dispar L. and the prospects
of using them.(In Russian). Zool. Zh. 35: 251-265.
Short, J.R. T. 1978. The final larval instars of the Ichneumonidae. Mem. Amer.
Ent. Inst. 25: 1-508.
Simons, E.E., Reardon, R.C., and Ticehurst, M. 1979. Selected parasites and
hyperparasites of the gypsy moth, with keys to adults and immatures.
U. S. Dept. Agri. Agri Handb. No. 540: 1-59.
Stadler, H. 1933. Ein neuer Ichneumonide aus Schwammspinnerraupen (Lymantria
dispar L.). Ent.Anz. 13: 27-30, 43-45, 58-60.
Stafanov, D. and Keremidchiev, M. 1961. The possibility of using some predators
and parasitic insects (entomophagous insects) in the biological control of the
gypsy moth (Lymantria dispar L.) in Bulgaria,(In Bulgarian). Nauch. Trud.
Vis. Lesotech. Inst. 9: 157-168.
Timberlake, P.H. 1912. Technical results from the gypsy moth parasite laboratory.
V. Experimental parasitism: A study of the biology of Limnerium validum
(Cresson). U.S. Dept. Agri. Bull. Ent. Tech. Ser. 19: 71-92.
Thompson, W.R. 1946. A catalogue of the parasites and predators of insect pests.
Section I. Parasite host catalogue. Part 8. Parasites of the Lepidoptera (N-P).
V. Gupta: Gypsy Moth Parasites 131
Thompson, W.R. 1957. A catalogue of the parasites and predators of insect pests.
Section 2. Host parasite catalogue. Part 4. Hosts of the Hymenoptera
(Ichneumonidae). CIBC, Ottawa. 9561p.
Townes, H. K. 1940. A revision of the Pimplini of eastern North America (Hy menop-
tera, Ichneumonidae). Ann.Ent. Soc. Amer. 33: 283-323.
Townes, Henry K. 1944-45. A catalogue and reclassification of the Nearctic
Ichneumonidae (Hymenoptera). Mem. Amer. Ent. Soc. 11: 1-925.
Townes, Henry 1969-71. The genera of Ichneumonidae, parts 1-4. Mem. Amer.
Ent. Inst, 11.012, 28, ane 27.
Townes, Henry and Marjorie, 1960. Ichneumon flies of America north of Mexico: 2.
Subfamilies Ephialtinae, Xoridinae, Acaenitinae. U.S. Natl. Mus. Bull.
216 (2): 1-676.
Townes, Henry and Marjorie, 1962. Ichneumon-flies of America north of Mexico: 3.
Subfamily Gelinae, tribe Mesostenini. U. S. Natl. Mus. Bull. 216 (3): 1-602.
Townes, Henry and Marjorie, 1978. Ichneumon-flies of America north of Mexico: 7.
Subfamily Banchinae, tribes Lissonotini and Banchini. Mem. Amer. Ent. Inst.
26: 614 p.
Townes, H., Momoi, S., and Townes, M. 1965. A catalogue and reclassification of
the eastern Palearctic Ichneumonidae. Mem. Amer. Ent. Inst. 5: 671 p.
Townes, H., Townes, M., and Gupta, V.K. 1961. A catalogue and reclassification of
Indo-Australian Ichneumonidae. Mem. Amer. Ent. Inst. 1: 502 p.
Tragardh, I. 1920. Investigations on the occurrence of the nun moth near Gulov in
1915-1917, (In Swedish). Medd. Stat. Skogsforsoksanst. Stockholm 17 (4):
301-328.
Uchida, T. 1930. Vierter und fuenfter Beitrage zur Ichneumoniden fauna Japans.
J. Fac. Agri. Hokkaido Imp. Univ. 25: 242-347.
Uchida, T. 1930. Beitrag zur Kenntnis der Ichneumoniden Fauna der Insel Izu
Oshima. Trans. Sapporo Nat. Hist. Soc. 11 (2): 78-87.
Uchida, T. 1941. Die Kriechbaumerschen Typen der Japanischen Ichneumoniden.
Trans. Sapporo Nat. Hist. Soc. 16: 227-230.
van Rossem, G. 1969. A study of the genus Meringopus Foerster in Europe and
some related species from Asia (Hymenoptera, Ichneumonidae, Cryptinae).
Tijdschr. v. Ent. Tig: 165-195,
Vasic, K. 1958. Parasitic Hymenoptera of gypsy moth (In Russian). Zast. bilja
41-42: 17-21.
Victorov, G.A. 1957. Species of the genus Enicospilus Stephens (Hymenoptera,
Ichneumonidae) in USSR (In Russian). Ent. Obozr. 36: 179-210.
Victorov, G.A. 1958. Material on the taxonomy of the ichneumon-flies of the genus
Encospilus Stephens (Hymenoptera, Ichneumonidae) (In Russian). Zool. Zh.
36; 215-221.
Viereck, H.L. 1911. Descriptions of one new genus and eight new species of
ichneumon-flies. U.S. Natl. Mus. Proc. 40: 455-480.
Walley, G.S. 1947. The genus Casinaria Holmgren in America north of Mexico
(Hymen. , Ichneumonidae). Scient. Agri. 27: 364-395.
132 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Wolff, M. and Krausse A. 1922. Die forstlichen Lepidopteren. Jena. 337 p.
Yafaeva, 1959. Ukrainskaya Akad. Selsk. Nauk p. 227. (not Seen).
Yasumatsu, K. and Watanabe, C. 1964. A tentative catalogue of insect natural
enemies of injurious insects in Japan. PartI. Parasite-Predator Host
Catalogue. Ent. Lab. Kyushu Univ., Fukuoka, Japan. 1166p.
Due acknowledgment is made here for the use of certain figures from published
sources, as indicated below:
Townes (1969-1971) (Figs. 1-6, 43-48, 68, 74-77, 80-84, 87, 90, 114-121).
Finlayson and Hagen, 1979. Final instar larvae of parasitic Hymenoptera.
Pest Management Papers No. 10, SFU. (Figs. 122, 123, 138-141).
Howard and Fiske, 1911. (Fig. 61),
Kaur and Jonathan, 1979. (Figs. 69-73).
Kasparyan, 1981. (Figs. 85, 86, 88, 89).
Perkins, 1960. (Figs. 91-113).
Short, 1978. (Figs. 124-137).
van Rossem, 1969. (Figs. 78,79).
V. Gupta: Gypsy Moth Parasites 133
COCCYGOMIMUS madecassus
— } WLe
op Me; ee :
<I i ITOPLECTIS tite Ne.
7
ii a SY \
2 Le XN SS S&S
4)
Figs. 1-2. Generic diagrams of: 1, Coccygomimus.
2, Itoplectis.
134 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
ee THERONIA atalantae bh) "
Figs. 3-4. Generic diagrams of: 3, Ephialtes.
4, Theronia.
V. Gupta: Gypsy Moth Parasites 135
ISEROPUS stercorator
GREGOPIMPLA inquisitor Sa 6
Figs. 0-6. Generic diagrams of: 5, Iseropus.
6, Gregopimpla.
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
136
i
eS
.
llae.
edal
ione
tur
]
Coccygomimus
C. disparis. 1
1,
10.
{
1ew Oo
tigator.
i
front v
ns
Cc
?
9
it
Head
9
lternans.
7-12.
moragues
oplectis a
Figs.
8, C.
12, It
V. Gupta: Gypsy Moth Parasites 137
Figs. 13-18. Thorax, side view of: 13, Coccygomimus turionellae.
14, C. moraguesi. 15, C. instigator. 16, C. disparis. 17, C. pedalis.
18, Theronia atalantae fulvescens.
Contrib. Amer. Ent. Inst:, vol. 19, no. 7, 1983
138
LS:
|
GO
rm)
oe
o e
Slo|
pod
® nr
cle
OlN
opel
mM .
Blu
opal
Oe
Es
i
ort |
Slo
one
Ho|
= n~
olny
O
Oo
rc O
=e)
ext
wD
So
= ee
= 5
6 UO
S's od
ra
Ha
ee
0
ort | SN
-
+ o|8
Q Ble
for)
& is
ei Ke)
yg Ale
OO wc
CT |
& OF
o>
aa
V. Gupta: Gypsy Moth Parasites 139
Figs. 25-30. First abdominal tergite of: 25, Coccygomimus turionellae.
26, C. moraguesi. 27, C. instigator. 28, C. disparis. 29, C. pedalis.
30, Itoplectis alternans.
140 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Figs. 31-36. Tergites 2 and 3 of: 31, Coccygomimus turionellae.
32, C. moraguesi. 33, C. instigator. 34, C. disparis. 35, C. pedalis.
36, Itoplectis alternans.
V. Gupta: Gypsy Moth Parasites 141
Figs. 37-42. Propedeum of: 37, Itoplectis alternans. 38, I. conquisitor.
Side of thorax of: 39, I. alternans. 40, I. conquisitor. Tergites 1 to 3 of:
41, Theronia atalantae. 42, I. conquisitor.
142 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
44 ee CAMPOPLEX hyalinus Sy
Figs. 43-44. Generic diagrams of: 43, Sinophorus.
44, Campoplex.
V. Gupta: Gypsy Moth Parasites 143
CASINARIA tenuiventris
ve CAMPOLETIS tibiator
46 fi
Figs. 45-46. Generic diagrams of: 45, Casinaria.
46. Campoletis.
1444 Contrib. Amer. Ent. Iist., vol. 19, no. 7, 1983
oP y
iS ae PERIOD oF
HYPOSOTER synchlorae
nO ee ee
a
165. PHOBOCAMPE geometrae
48
Figs. 47-48. Generic diagrams of: 47, Hyposoter.
48, Phobocampe.
V. Gupta: Gypsy Moth Parasites 145
Figs. 49-54. Phobocampe unicincta: 49, Propodeum. 50, Vertex.
51, Face. P. lymantriae: 52, Propodeum. 53, Vertex. 54, Face.
Contrib. Amer. Ent. Inst., vol. 19, no 7, 1983
146
iew.
oo, Side v
Phobocampe lymantriae, tergites 1-2
Figs. 55-58.
96, Dorsal view.
view.
08, Dorsal
lew.
ov, side v
ta, tergites 1-2:
unicinc
i.
V. Gupta: Gypsy Moth Parasites 147
62
Phobocampe unicincta: 59, Adult. 60, Egg. 61, Cocoon.
62, Larval mandibles, A-E. First to fifth instars.
Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
148
:
ee
:
_
|
A _.
_
:
:
Propodeum.
9
tH
CO
a
S)
qs}
Fy
«a OD)
Gy. 1
CON
——
wn
® |
2) bp
all OD)
Sie
eS) nw
it
$4 |co
+
Sy F
Olr
a
ae
OlEp
Oui sy
>| Oo
oi (=
avon
~ ©
|
Om .
co
a:
No
O) ct
ord
fr,
lO
CO
V. Gupta: Gypsy Moth Parasites 149
>,
on
pgs) WE ET ET Gee
<x i ae
S
a
LO
71
Figs. 68-73. 68, Generic diagram of Netelia.
N. vinulae: 69, Vertex. 70, Head, front view.
71, Propodeum. 72, Part of front wing. 73, Areolet.
150 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
GAMBRUS incubitor
ISCHNUS inquisitorius
xg
Figs. 74-76. Generic diagrams of: 74, Gambrus.
79, Ischnus. 76, Ovipositor tip of G. amoenus.
V. Gupta: Gypsy Moth Parasites 151
— ) 77
Sa ar coor
MERINGOPUS relativus
pee
BANCHUS pictus = —=
Q J
Figs. 77-80. 77, Generic diagram of Meringopus. 78, M. cyanator,
head. 79, Hind wing of same. 80, Generic diagram of Banchus.
152 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Figs. 81-82. Generic diagrams of: 81, Pristomerus.
82, Ophion.
V. Gupta: Gypsy Moth Parasites 153
ne TRICHOMMA fulvidens Me
Ran
SD
\ Sa,
5 N
Figs. 83-86. Generic diagrams of: 83, Enicospilus.
84, Trichomma. T. enecator: 85, Vertex. 86, Face.
154 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
gen FER Ee Pa
os Ce
DS
S
87 BARYLYPA elongata
a
sS
oS
on
aS
es
oo
——_
S
yp
90. ae
Figs. 87-90. Generic diagram: 87, Barylypa.
88, Hind tarsus B. delictor. 89, Male clasper,
B. delictor. Generic diagram: 90, Agrypon.
AGRYPON flaveolatum
V. Gupta: Gyspy Moth Parasites
155
' Hy |
dtl i
|
| ‘
tipa
i He
Natt
mea a |
Dowel!
p< SO ehepe:
CP PK
RELL oO
' iS
; Beery
t %. Sy
t
Figs, 91- 99. Callajoppa cirrogaster: 91, Propodeum.
92, Vertex, 93, Flagellar segments. 94, Clypeus.
Melanichneumon leucocheilus: 95, Clypeus, male. 96,
Clypeus, female. 97, Head. 98, Tergite 2, 99, Ptero-
cormus sarcitorius, abdomen color, be
156 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Etat
SECS
RRR Ses
111 112 M13
Figs. 100-113. Triptognathus amatorius: 100, Abdomen color.
101, Tergites 2-3. 102, Male penis valve. 103, Mandible.
Spilichneumon occisor: 104, Hypopygium. 105, Basal flagellar
segments. 106, Mandible. 107. Penis valve. 108, Pronotum.
109, Male propodeum. 110, Female propodeum. Amblyteles
armatorius: 111, Propodeum. 112, Abdomen. Pterocormus
sarcitorius: 113, Postpetiole.
V. Gupta: Gypsy Moth Parasites 157
Figs. 114-115. Generic diagrams of: 114, Ichneumon,. 119,
Melanichneumon.
158 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
SE.
J
Figs. 116-117. Generic diagrams of: 116, Spilichneumon. 117,
Cratichneumon.
V. Gupta: Gypsy Moth Parasites 159
aS. 118 Ray : S
* a
Figs. 118-119. Generic diagrams of: 118, Chasmias. 119,
Triptognathus.
160 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
| . va
a 120 S ee
Figs. 120-121. Generic diagrams of: 120, Pterocormus. 121,
Cotiheresiarches.
V. Gupta: Gypsy Moth Parasites 161
Vacuole
Labral sclerite
Suspensorial sclerite
Epistoma (incomplete)
Antennal socket
Antenna
Superior mandibular process
Mandible
Pleurostoma
Teeth
Lacinial sclerite
Inferior mandibular process
Dorsal flange
Sensorium
Maxillary palp
Hypostoma
Hypostomal spur
Stipital sclerite
Dorsal arm of labial sclerite
Labial sclerite
Labial palp
Blade of mandible
Silk press
Prelabial sclerite
Figs. 122-123. 122, Nomenclature of cephalic sclerites of the
ichneumonid larval head. 123, Larval head of Coccygomimus pedalis.
162 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
: —— Ps CO ae ee Ba
~~ ~~ RF werRaeae ~
e
124 Coccygomimus turionellae with posterior view of left mandible
frend
125 Coccygomimus spurius
Figs. 124-125. Larval head of : 124: Coccygomimus
turionellae. 125, C. spurius.
V. Gupta: Gypsy Moth Parasites 163
ltoplectis alternans
Itoplectis conquisitor
Figs. 126-127. Head sclerites of larvae.
164 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
128 Ephialtes compunctor
Ephialies rufatus
Figs. 128-129. Head sclerites of larvae.
V. Gupta: Gypsy Moth Parasites 165
130 Gregopimpla inquisitor with sclerotized
(=) intersegmental ring oy |
131 lseropus stercorator stercorator
Theronia atalantae atalantae
Figs. 130-1382. Head sclerites of larvae.
166 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
Netelia (Netelia) vinulae
Casinaria tenuiventris
Figs. 133-135. Head sclerites of larvae.
V. Gupta: Gypsy Moth Parasites 167
ote
rs S,
eN
138 Banchus femoralis
Figs. 136-138. Head sclerites of larvae.
168 Contrib. Amer. Ent. Inst., vol. 19, no. 7, 1983
141 Mesochorus fulgurans
Figs. 139-141. Head sclerites of the larvae.
Errata to: Gupta, Virendra, 1983. The Ichneumonid Parasites Associated with the
Gypsy Moth (Lymantria dispar) - Contrib. Amer. Ent. Inst. 19 (7): 1-168.
References inadvertently left out . To be inserted on pages 124 to 1382.
Gauld, |. D. and Mitchell, P. A. 1977. The Orthopelmatinae and Anomalolinae. Handbooks
for the Identification of British Insects. 7, 2b: 1-32.
Gupta, V. K. 1970. Ichneumon Hunting in India. A report of the work done under
P.L. 480 research project ... on Ichneumonidae in India. Delhi. Pp. 1-109 +
appendix 1-80.
Gupta, V.K. and Tikar, D.T. 1976. Ichneumonologia Orientalis, Part |. The tribe
Pimplinae (Hymenoptera: Ichneumonidae). Oriental Insects Monographs
1: 32.
Fahringer, J. 1922. Contributions to a knowledge of the habits of seme parasitic Hymen-
optera with specia! regard to their importance in the biologica! control of
injurious insects. Z. Angew. Ent. 8 (2): 325-388. (in German).
Nagaraja, H., Dharmadhikari, P-R., and Rao, V. P. 1969. A comparative study of the
external morphology of Lymantria obfuscata Wlk. in India and L. dispar (L.)
in the U.S.A. Bull. Ent. Res. 59: 105-112 (1968).
Rudow, F. 1888. Einige neue Ichneumoniden. Ent. Nachr. 14: 83-92, 120-124, 129-136.
Uchida, T. 1926. Erster Beitrage zur Ichneumoniden Japans. J. Coll. Agri. Hokkaido
Imp. Univ. 18: 43-1783.
Uchida, T. 1958. Shin Konchu 8(5): 8.
Walkley, L. M. 1958. Family Ichneumonidae. In: Krombein, K.V. (Ed.) Hymenoptera
of America North of Mexico Synoptic Catalog First Supplement to Agri.
Monogr. 2. U. S. Dept. Agri. Washington. Pp. 36-62.
P. 132. Under acknowledgment for illustrations add Muesbeck and Parker, 1933
for figures 59, 60 and 62.
Corrections
Page 4 Line 12 from bottom For Lerut (1980) Read Leraut (1980)
11. Under species 10 Add (1933) after Morley and Rait-Smith
14 i EF 4 For page 77 Read page 75
12 ie 23 For Rudow (1933) Read Rudow (1918)
14 Line 15 from bottom ,, Nagaraja et al (1968) Read Nagaraja et al. (1969)
104 Line 11 and 36 For Kolubayiv Read Kolubajiv
105 Line 9 For Gupta (1973) Read Gupta (1970)
110 Line 7 from bottom For Kraube Read Krausse
12 Line 6 For Delrio (1974) Read Delrio (1975)
118 Line 3 from bottom For Kraube Read Krausse
124 Line 4 from bottom For Res. Read Rec.
127 Reference to Kovacevic Z. should come after Kolabujiv on page 128
Please let me know if you discover any other omission or correction.
Virendra Gupta
Ne och:
Pee gaa .
city's) ee
Seen
Cea
nwa
ie
Ply cht Vite seve WF Wiest sa Fo Nida Fue ine,
oe) \ “TP, a i
Th sarge ha He
5 sty
amd] el
ced ay
ans
vgn *
at
er
ste
at
A Synopsis of the World Species of
Desmometopa Loew (Diptera, Milichiidae).
Curtis W. Sabrosky 1/
Systematic Entomology Laboratory,
Agricultural Research Service, U.S. Department of Agriculture
ABSTRACT
The genus Desmometopa Loew is revised, with the number of recognized
species in the world raised from 10 to 51, divided for the first time into two
‘subgenera, Desmometopa Loew and Platophrymyia Williston. The classification,
identification, morphological characteristics, and biology of adults and larvae are
discussed, with numerous new rearing records. A key is provided to the 51
species, 41 of them new, of which 8 are left unnamed because of inadequate
material. Two new synonyms are proposed, a queried synonymy is confirmed, and
4 lectotypes are designated.
CONTENTS
Ey PRACT IO) Mian saicaeten ade we og cna abirerel spe cha aod Sh RIS Veen att ae i Hees 2
Wet Ch aeaa tt bt alos ule. acide olay alban 4 elves sua yy aap x hema iace bv cues RRNA EET ee the ceo 2
AT OMNI oe) ladies tuen se uualen dla lbapiinaichesnheedane thx hud de eiRid «paar n ta peae ceva aie 4
Morphological Characteristics............. Sica aetEd SRT AS side eons ORL AN RORY «EEG A 5
ibenlesty yf thre Pocdsal Geek sis sa vcnntic vate igus es Pecawceen ens veinsn ch tubawan eee Cemeta< ames) sewnnaes 9
Cahir 1 LUN A ME VO issih silo ve Adis aks dina AN who La WRC Ree 15H 0 NRTA RAE NR ARO Ea neve 10
Sears cues AG UTI GL) Juin inn xazncecd vn bine ntling Anta Wh een Na vO da Oe Read AAA Tag Oe 12
DECI Gin «cis x nh isinien aid tdy a veewcabiids soi kph oon itu V eae ieians Bees L Oh GGised ves dont 12
See O ALOR LIE Wisin suwkl do cndasavasbetdins oinkeld oeahenkersnnneasdnasicbibing as adseuleeeenine cos chavenynd’s 13
MEY TO: THE: WORLD SPECIES OF De@emometopeeiicens. <uvsdcchasdecasewsssubancadseaeneaveee 14
SS TPE AT NEI awa cin eager PERE hia doe 21
(See Index for individual species)
SPECIES OF "Desmometopa” NOW REFERRED ELSEWHERE. .............ccecccceeccces 62
bey La itearetrie eed res oY TB a havin witu tpalbtecn 4 ons gd Sen io Gi Nie da Onn bw RRNA LENO Ue ker hen RTA eS ees 64
Pe iii J se dew ruc uidimy eas puutaded aha eul «Adria eel ae aud as cia ben ashes eas cues 66
NO cecesucveceenls Cuticle ea Ciiodias ren Gee RD Cie OO Es 69
T/ Mailing address: Systematic Entomology Lab., USDA, c/o U.S. National
Museum, Washington, D.C. 20560.
2 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
INTRODUCTION
The small black flies of the dipterous genus Desmometopa Loew are
commonly encountered in all faunal regions, and they form a delightfully
recognizable group of species because of a black M-shaped frontal vitta
delineated by gray frontal triangle, fronto-orbital plates, and two straplike
interfrontal plates (figs. 1,2,10). The genus is easily placed in available keys to
the genera of Milichiidae (e.g., Hennig 1937). However, some confusion in
identification of the species has long indicated that a synopsis and usable key
were badly needed.
Classification
For some years, the genus Desmometopa included species now referred
elsewhere, notably to Leptometopa Becker, Stomosis Melander, and
Neophyllomyza Melander, none of which has the inter—frontal plates although they
may have rows of fine setae in the same positions. As recognized for over six
decades, however, the genus has been confined to those species having the two
straplike or bandlike interfrontal plates, with 17 proposed specific names well
scattered from 1820 to 1965. In the present study these are reduced to 10 species
and 7 synonyms, only 4 of the recognized species being common. The present
study recognizes a total of 51 species, including 41 new species, chiefly
Neotropical, well over half of these in the “tarsalis complex". Eight of the 41 are
left unnamed at this time, however, because of the inadequacy of available
material, but they have been included in the key. I am inclined to believe that
even more species will be discovered, as has often been the case in other genera
of neglected or overlooked small black flies.
The contrast with recent literature is striking. Modern catalogues for the
Nearctic, Neotropical, Oriental, and Afrotropical Regions (Sabrosky, 1965b, 1973,
1977, 1980) listed, respectively, 3, 6, 6, and 8 species, and Duda (1935) recognized
4 Palearctic species. Eliminating duplications, a total of 12 species was
recognized, and 3 of these are dropped as synonyms in the present classification.
The discovery of several polished black Neotropical species that might belong
to the genus inevitably raised questions about their relationship to Desmometopa
and to Litometopa Sabrosky, the latter proposed for a single species from
Tanzania. Neither Litometopa nor the polished Neotropical species have
interfrontal stripes, but the Neotropical species have 2 rows of interfrontal setae
in contrast to their complete absence in Litometopa. Possibly these are degrees
of reduction from the interfrontal plates of Desmometopa, but I prefer here to
retain the distinctness of the plates as uniquely characteristic of Desmometopa.
The polished species may represent a new genus. I may add that Litometopa has
other distinct features: only one upper and one lower fronto-orbital bristle on
each side; no presutural bristle, and mesonotum almost bare of hairs except for
the median acrostical and dorsocentral rows and a few intra-alar hairs, whereas
the polished black Neotropical species resemble Desmometopa in all these
features.
The genus may be divided into two subgenera on the basis of the structure of
the head:
Subgenus Platophrymyia Williston (type species P. nigra Williston, which is a
synonym of OD. tarsalis Loew, a commonly used--and all too frequently
misused--name): Vibrissal angle distinctly produced anteriorly to about a 45°
angle (fig. 18), the angle emphasized by shining black lateroventral corner of
facial plate, immediately mesad of vibrissal angle and usually warped forward and
upward beyond it. Lower margin of head comparatively long and face deeply
Sabrosky: Desmometopa of the World 5
concave as seen in profile. Epistomal margin, the lower margin of face, more or
less strongly warped upward also, and especially so on the midline so as to shorten
the face between epistomal margin and apex of the lunule between antennal
bases, this warping and shortening, together with a distinct medial facial carina,
all combining to accentuate the concave antennal grooves or foveae.
Subgenus Desmometopa s. str. (type species Agromyza m-atrum Meigen, a
synonym of D. sordida (Fallén): Vibrissal angle not produced anteriorly, only an
80° to 90° angle (e.g., figs. 3,5,6-8), face only slightly concave as seen in profile,
the latero-ventral corner of facial plate dull gray like rest of face, and not
warped forward. Epistomal margin at most only slightly warped forward and
upward, usually not markedly so at midline, the face not materially shortened on
midline, facial carina weak, and antennal foveae not accentuated.
Most of the species fall easily into one or the other of the two groups. The
characteristics of a few species seem to be somewhat intermediate, or could be
misinterpreted by someone using the key without adequate reference material or
experience. Accordingly the subgeneric division is not used initially in the key,
which is intentionally artificial to bypass some problem species and give priority
to accuracy of identification.
3 The species can be assigned to subgenera as follows, with geographic
distribution indicated by faunal regions (Oceanic = the Pacific islands):
Subgenus Desmometopa Loew (22 species)
Widely distributed:
inaurata (Afrotropical, Neotropical, Australian, Oceanic), microps
(Afrotropical, Palearctic, Oriental, Oceanic), m-nigrum (Holarctic,
Neotropical, Afrotropical, Oriental, Australian), singaporensis (Oriental,
Oceanic, Afrotropical, Palearctic, Neotropical), varipalpis (Australian,
Oceanic, Oriental, Sa aloiace Palearctic, Nearctic, Neotropical).
Holarctic: sordida.
Palearctic: sp. H.
Afrotropical: aldabrae, interfrontalis, Hale ees ite magnicornis,
nudigena, pleuralis, postorbitalis.
Oriental: philippinensis, propeciliata, srilankae, spp. L,M,N.
Australian: ciliata.
Oceanic: terminalis.
Subgenus Platophrymyia Williston (29 spp.)
Nearctic: floridensis, latigena, melanderi, nearctica, parafacialis, saquaro,
sp. 0.
Neotropical: aczeli, argentinica, atypica, blantoni, evanescens, flavicoxa,
glaucanota, indistincta, lucidifrons, meridionalis, | niqrohalteralis,
obscurifrons, stilbopleura, woldai, spp. I,J,K.
Neotropical to Oceanic: tarsalis.
Oceanic: flavipalpis, gressitti.
Oriental: kandyensis.
Afrotropical: nigeriae.
Five species of the typical subgenus are widely distributed, apparently having
been spread in commerce, and D. tarsalis in Platophrymyia has moved out into the
Pacific islands from its Neotropical homeland. Otherwise, except for a few
unexplained species in Platophrymyia, the two subgenera make a fairly good
separation between Old World (Desmometopa) and New World (Platophrymyia)
species.
4 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
There are a number of records of adult Desmometopa being collected on ships
and planes (e.g., see varipalpis), and it has been suggested that this indicates how
some species were distributed widely in commerce. Another possibility is
indicated by the rearing of varipalpis at New York from larvae in potatoes in a
ship from Argentina, and of singaporensis in Fiji from onions imported from
Australia.
Desmometopa is clearly a name of feminine gender, not neuter as it has often
been used in such combinations as D. sordidum. Loew's first species included in
the genus was D. tarsalis, which could indicate either masculine or feminine
gender, but certainly not neuter. In his accompanying note he used the feminine
ablative form "cui Desmometopae.” The distinguished European dipterists Hendel
and Becker, among others, in writing on milichiids around the beginning of the
century used D. sordidum, undoubtedly influenced by the specific names m-atrum
and m-nigrum; however, in these the adjectival ending -um (neuter) depends not
on the generic name but on the "m" which it modifies, and individual letters of the
alphabet are treated as neuter. Konow (1907) early pointed out that
Desmometopa was feminine. Grensted (1956) likewise argued that Desmometopa
was feminine, compounded with the stem of the Green metopon (a forehead),
which is neuter, but with an irregular termination -a that made the name
feminine. He followed a ruling of the International Commission on Zoological
Nomenclature (1958, Declaration 39), which was incorporated into the
International Code (1961, 1964) as Article 29c. |
For the record, and to assist in the proper placement of species listed in the
literature as "Desmometopa," species either described in or referred to that genus
at some period, but now referred elsewhere, are listed at the end of this paper
together with a discussion of the special case of Agromyza albipennis Meigen.
Identification
Misidentifications have been rife in Desmometopa, probably in part because
of the great similarity in appearance of many of the species. The two interfrontal
plates combine with the fronto-orbital plates and frontal triangle to divide the
frontal vitta into an M-shaped black area (M as viewed from in front), and this has
led to the frequent misuse of the name D. m-nigrum. An early error in using the
name D. tarsalis Loew for an Old World species resulted in many misidentifica-
tions, in addition to which the name tarsalis has been widely misapplied in the
New World because of failure to realize the large number of similar species in
what might be called the “tarsalis complex". In all faunal regions, taxonomists
have failed to appreciate the large number of species that actually exist in the
genus, aided and abetted by the belief--partly true--that several common
scavenger species had been widely distributed in commerce. Minor sources of
error have been the inability to distinguish females of singaporensis and
varipalpis, compared with their very distinct males, and lack of recognition of the
sexual dimorphism in the form of the head in microps.
A few examples will suffice. In one of the great New World museums, I found
five species identified as D. m-nigrum: true m-nigrum (most of the specimens,
fortunately), a few of sordida, and one each of tarsalis, varipalpis, and
Leptometopa latipes (Meigen), the latter probably only a curatorial lapsus.
Likewise in one of the great European museums there were five species under
m-nigrum: true m-nigrum (again, most of the specimens), sordida, varipalpis,
inaurata, and a new species near microps. "D. tarsalis" of Malloch's (1914) report
on Sauter’s Formosa-Ausbeute proved to be a mixture of singaporensis and
microps.
Sabrosky: Desmometopa of the World 5
The confused usage of names is vividly illustrated in Hawaii, where four
introduced species of Desmometopa are currently known to occur. The first
record of the genus from the islands, as far as I know, is that by Illingworth at the
Feb. 5, 1925 meeting of the Hawaiian Entomological Society (note published
1926), who published D. m-nigrum as "recently" identified by J. M. Aldrich from
specimens reared in 1916 "in abundance from macerated hen manure.” True
m-nigrum has never been found in Hawaii, however, and Aldrich himself corrected
his identification to D. tarsalis (see Illingworth 1929). Hardy and Delfinado (1980)
in the “Insects of Hawaii" record Illingworth's 1916 rearing in two places, once
under their "singaporensis" (based on an earlier identification by me), which is
varipalpis, and once under tarsalis, the original usage of Illingworth (on authority
of Aldrich). Both may be in error. The specimens in the U.S. National Museum of
Natural History reared by Illingworth and identified by Aldrich are singaporensis
as I recognize it, not "singaporensis" of Hardy and Delfinado (see discussion under
singaporensis). To complicate the picture still further, both true tarsalis and true
singaporensis are now known in Hawaii and one or both might also have been
present in Illingworth’'s material. For what it may indicate, however, true
_singaporensis was also reared from poultry manure in Hawaii years later by
Yoshinori Tanada, and I have no records of varipalpis from manure anywhere, and
only one record of tarsalis from manure, from cow manure in Guam.
As a result of such situations, published records with commonly used names
must be ignored unless the original specimens can be reexamined, at least outside
of the Holarctic Region in which the few species are well known. Ordinarily, for
the common species, enough specimens have been available to me that I can give
an adequate picture of the distribution without verifying or correcting individual
published records. If voucher specimens have been checked, however, I record the
fact.
The condition of specimens affects the usefulness of many characters. One
must ever be alert for immature (teneral) specimens in which proportions and
color are unnatural. In particular, the proportions of the head can be greatly
affected, especially the breadth of the cheek and the angle of the vibrissal angle.
If the face is collapsed, it becomes more concave as seen in profile, and the
vibrissal angle may thus appear to be produced and acute. Identification of such
examples should be done with caution and attention to other characteristics.
Morphological Characteristics
All species have a= similar habitus and community of structure and
chaetotaxy, and a full description under the genus permits rather brief
descriptions for the species, with concentration on characters differing most
among the species. A few comments on these are in order.
Microtomentose: The dorsum of the thorax and parts of the pleuron are
densely gray to brownish gray, over the black ground color. This has usually been
referred to as pollinose or pruinose or "dusted", but analysis shows that the areas
are actually covered with microscopic outgrowths of the cuticle, sometimes
curled or curved like minute microtrichia. The terms pollinose and pruinose seem
fundamentally inappropriate, and in recent papers I have used the term
“tomentose”. However, this may imply to some readers woolly or matted hair,
and I suggest, and use here, the term microtomentose.
The frons almost always appears slightly longer than broad at vertex,
especially in males. Measurements confirm this, although the quotient for longer
than broad is usually not as great as anticipated, often only up to 1.2 times. I
have mentioned it only for a few extreme cases. Aside from lengths and widths
6 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
of interfrontal plates, fronto-orbital plates, and frontal triangle, which need no
explanation, the appearance of the M-shaped frontal vitta is a most useful
character. In two species, the entire frons is uniformly dull brownish or brownish
gray, obscuring all plates and the frontal triangle and making these species
unusual and aberrant in the genus. Most other species have the frontal vitta
velvet black, sometimes slightly subshining, against which background the other
parts stand out distinctly. In a number of species (tarsalis and relatives) most of
the frontal vitta is gray microtomentose, although not densely so, from at least
certain angles.
The frontal triangle is not a definite sclerotized plate, as in most
Chloropidae, but nevertheless the triangular microtomentose area is as regular
and consistent as the interfrontal plates. It is a continuation of the
microtomentum regularly present on the ocellar tubercle. Occasionally the
tomentum barely extends beyond the median ocellus, or it may extend far forward
between the interfrontal plates to midway of the frons (fig. 10).
The term cheek (rather than gena) is used here for the combined gena plus
subgena below the eye. If gena is correct for the upper part of the cheek, it
should not be used for the entire area, even though in these tiny flies the subgena
is linear and gena s.str. is almost coextensive with cheek. The breadth (height) of
the cheek compared to the breadth of a 3rd antennal segment and to the vertical
height of an eye are useful characteristics, as well as the development of a
polished area along the lower margin of the eye that I propose to call the
subocular crescent (cf. figs. 7 and 14 for extremes). Without actual measurement,
one can more easily perceive the proportion of cheek to 3rd antennal segment
than that of cheek to the much higher and very convex eye, where optical illusion
can deceive. However, the antennae are easily knocked off and are often missing
in available specimens that are otherwise in good condition, but the cheek:eye
relationship can always be determined.
In the row of subgenal setae along the lower margin of the head, the first or
second behind the vibrissa is developed in a few species as a strong upcurved
subgenal bristle, e.g., in D. ciliata (fig. 11). In most species, the setae form an
even row, gradually becoming longer and stronger towards the vibrissa.
The postorbital (dorsal) and postgenal (ventral) areas are usually narrow but
in a few species one or both are broader than usual, and in males of one species ©
(microps, fig. 17) they are convex and appear bulging.
The produced vibrissal angle (fig. 18) is explained under the division into
subgenera. The area immediately mesad of the vibrissal angle has no special
name and I have referred to it, hopefully accurately albeit long and somewhat
awkwardly, as the lateroventral corner of the facial plate. In the subgenus
Platophrymyia (fig. 18), it is shining black although not smooth and polished, the
shine interrupted by fine lines. The warping forward and upward of this area and
the whole epistomal margin is distinct and even exaggerated in large specimens,
but less distinct and unimpressive in small specimens.
In most species, each 3rd antennal segment is only a little broader than the
2nd segment, and it is referred to in the descriptions as “small.” In three new
species, however, the 3rd segment of the male is conspicuously enlarged (fig.
21)(see the supplemental "key to males with unusual features”). Other species
presently known only from females may also show this, especially the small
species with blackish halteres that seem closely related to the three just
mentioned.
The palpi are usually gently clavate (e.g., fig. 18), gradually broadening from
base to apex, but in a few species they are broad and flat (fig. 4), unusually long,
with the development more striking in large specimens. In a few species, the
males have unusually long and distinctive palpi (see special key for such males,
Sabrosky: Desmometopa of the World 7
and cf. figs. 3 and 5). The color of the palpi is often useful, but one can also be
deceived. Species with palpi entirely or almost entirely yellow in both sexes, or
black in both sexes, are easy to separate. Between those extremes are species
with yellow or predominantly yellow palpi in males but with palpi half or more
infuscated in females. Occasional specimens of the latter have the palpi entirely
infuscated, and while this apparently involves only a small proportion of the
specimens, it does diminish the usefulness of the color as a character for the key.
Except for one possible exception (sp. H), the broadly flattened palpus (cf. fig. 4)
is found in some species of subgenus Platophrymyia.
The geniculate proboscis appears slender in side view, but in dorsal or ventral
view the haustellum is often broadened, especially toward the base. It is usually
slightly longer than the lower margin of the head and is mentioned only if
unusual. The labella are almost always a little shorter than the haustellum, but
because they are soft and their condition of expansion differs greatly among
individual specimens it is useless to mention comparative lengths. They almost
always appear slender, but in reality they are like a furled sail and occasionally
specimens will have them expanded nearly to the width of the oral cavity. This
_ should not be interpreted as a specific distinction.
The propleuron is rounded anteriorly in most Desmometopa, but some show
part of a ridge dorsally, just below the humerus. In some, there appears to be a
ridge on a line between a gray, microtomentose part and a polished anterior
declivity, but this line may have appeared more like a ridge because of drying of
the specimen. A strong propleural carina is characteristic of the family
Chloropidae, and the ridge in these species of Desmometopa might confuse the
unwary. It does suggest relationship between the two families, as indicated by
recent authors.
The polished areas on the pleuron (figs. 23-27) did not impress me at first,
and indeed such a careful observer as Hennig made no mention of them in his
monograph of the European species (1937). I have found these polished areas
surprisingly uniform within each species throughout the genus, even in such an
apparently insignificant and easily overlooked place as the small concave post-
spiracular area. The spots may have been misinterpreted as rubbed areas and
therefore of no importance. The polished spot on the pleuron posterodorsad of the
fore coxa is sometimes difficult to see because the femur at rest is over it and
close to the body. In most species the area is large enough that one can usually
glimpse it between femur and pleuron, but in species with a small spot, such as
interfrontalis, singaporensis, and varipalpis, one could easily miss it and key to the
few species that truly have an entirely microtomentose pleuron. Luckily,
interfrontalis has a distinctive pattern on the frons, and the common singaporensis
and varipalpis have yellowish cheeks and in the males uniquely distinct palpi, and
the chance of misidentification because of missing the pleural spot is almost nil.
The figures are somewhat stylized and semi-diagrammatic, but they illustrate the
major different types of polished areas.
The color of the tarsi needs particular attention. Tarsi that appear yellowish
in ventral aspect may actually be infuscated dorsally. Truly yellow tarsi are
yellow viewed from any angle. Specimens that have been mounted out of alcohol
will almost always be paler. Even though the sharpness of the character is not
always all that could be wished, nevertheless it is often useful to distinguish
‘between entirely infuscated tarsi, chiefly yellow tarsi (except for distal tarsomere
or two), and species with fore tarsus infuscated and mid and hind tarsi chiefly
yellowish.
Yellow fore coxae set off the flavicoxa group, all Neotropical species.
Species with black fore coxae are regularly and unquestionably so, but in very
teneral specimens the coxae may not be fully colored and one might think they
8 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
were yellowish. It is a good general rule to be cautious in dealing with teneral
individuals.
In most species, and in almost all females, the fore coxa is short and convex,
and the fore femur is not significantly longer than mid and hind femora. In a few
species (e.g., saguaro and melanderi), the fore coxa and fore femur are strikingly
elongate and raptorial or mantislike in appearance (cf. fig. 22). In others, they
are slightly to moderately elongate. Within any given species that shows
elongation, large specimens show it more distinctly than small ones.
The halteres usually have the stalk brown, but the knob may be lemon yellow
or whitish yellow, or it may be brown to blackish. The color of the knob is
actually an excellent specific character, especially for mature and clean
specimens. Unfortunately, many specimens, especially those from _ tropical
countries, are cleared from fluid, or are teneral, and the halteres are paler than
normal and can be misinterpreted.
The length is variable, and precision is difficult at best, but the approximate
length is given in order to distinguish in a rough way between the relatively large
and stocky species and the tiny species.
Male genitalia: Males of 32 species were dissected, including 13 of the
subgenus Desmometopa and 19 of the subgenus Platophrymyia. The genitalia of
all are strikingly similar, including those of such widely different species as
varipalpis and singaporensis on the one hand and tarsalis on the other, and they
have not been described for each species. The postabdominal and genitalic
characters agree with the characterization of Griffiths (1972) in most
particulars. The postabdomen and genitalia are completely symmetrical. There is
no full pregenital sclerite between the 5th segment and the hypopygium, rather
only a lateral band of sclerotization along each side of the epandrium. Spiracles 6
and 7 lie in the membrane alongside each of these bands. The bristly cerci are
unusually large, convergent ventrally in dissected specimens, as noted by
Griffiths, but in dried specimens the mesal margins are parallel and adjoining so
that under ordinary magnification they appear as a single shining slightly convex
line. This is quite different in appearance from the female abdomen so that
unless the abdomen is damaged or collapsed one can almost always be sure of the
sex of a specimen without dissection, even though the genitalia are tiny. The
epandrium bears on each side a single surstylus, partly fused with the epandrium.
The hypandrium is relatively small and slender, incomplete dorsally, the dorsal
ends of the arms of the hypandrium bifid. The aedeagus has a short basiphallus
(phallophore of Griffiths) and a long and weakly sclerotized to membranous distal
section, the two folding back at rest against the long and slender aedeagal
apodeme.
Sternites: Dissection of the male abdomens for genitalia revealed more
differences in the shape and setation of the sternites, especially of the 5th, than
in the genitalia. In most species examined, the 5th sternite was nearly square or
broader than long, but in lucidifrons and kandyensis it was decidedly longer than
broad. The 5th sternites in some species showed numerous discal setae, up to
70-80 in 8 or 9 very irregular rows, e.g., in ciliata, while others showed few and
sparse discal setae, even as few as 4 or 6 (indistincta and parafacialis). Because
of the similarity of the male genitalia, relatively few specimens were dissected
and the range of variation in shape and setation cannot be stated positively. I
would expect variation in the number of discal setae, but consistency in the
general pattern of few vs. many setae.
Sabrosky: Desmometopa of the World 9
Biology of the Adults
Adult Desmometopa are recorded as visiting various flowers, sometimes in
numbers, and they are also taken occasionally in light traps, including black light,
and in Medfly traps, Steiner traps, and “fruitfly traps." Numerous collections of
adults of D. varipalpis show their attraction to odors: "hospital laboratory”
(Reading, Penn.), “adults entering sterile operating and surgery area" (Peru, Ind.:
John Sillings), “in hospital operating room" (Ogden, Utah: J.B. Marsh), in a Dairy
Cheese room (Clovis, N. Mex.: B. Dictson), “in urinal" (Austin, Tex.: M.R.
Wheeler), “over outdoor latrine” (Mona I., West Indies: W.F. Pippin), “in septic
tank” (Khartoum, Sudan), “ex latrine” (Saipan), "on mud at edges of sewer effluent
beds" (Phoenix, Ariz.), “privy trap" (Savannah, Ga.: H.R. Dodge), “abundant in
butcher shop" (Austin, Minn.), and a huge number “collected dead in plastic about
trunk containing Cannabis sativa (San Francisco, Calif.: Terry Coddington, J.F.
Williams, P.H. Arnaud, Jr.). D. singaporensis was commonly "collected on
decaying giant African snails” (Palau Is., Koror: C.W. Sabrosky), and this species,
as “tarsalis", was collected on Guam on several occasions as “feeding adults from
human excrement” (Bohart and Gressitt 1951). In South Africa (Transvaal), D.
m-nigrum was collected off an Impala carcass (L. Braack), and in Ohio they have
occurred in great numbers in poultry houses (C.A. Triplehorn). One record that
may be open to some doubt: D. varipalpis was reported by employees of a filling
station in Riverside, Calif., to be “very annoying and hovering around the
faces...and occasionally getting into the eyes.” This habit is that of Hippelates
flies (eye gnats), and perhaps the wrong flies were collected and charged with
being the culprits. On the other hand, a female of D. singaporensis was collected
in Manila, Philippine Is., October 1928, by R.C. McGregor, who pinned this note to
the specimen: "The small fly kept pestering me--tried to get into my eye."
Perhaps the records do suggest annoyance at times or under some circumstances.
Another interesting habit of the adults is the phoretic relationships that have
been observed with predacious insects and spiders, in which adults of
Desmometopa-~-as well as some other milichiids--feed on the juices of the prey.
Knab (1915) reviewed a number of these observations, as did Peyerimhoff (1917),
who added two observations of small flies on the bodies of the prey of asilids. In
one case the small flies covering the body of the prey, a bee, were identified as D.
m-nigrum. Subsequently, Rabaud (1924) recorded an interesting case of 2.
sordida riding not on the body of a dead bee that was prey, but upon the pollen
“patée” on the hind tibia of a live bee, and apparently feeding at the pollen paste.
Richards (1953) observed D. sordida on a dead honey bee being sucked by a
reduviid, and he later captured specimens of the same species sitting on the same
species of bug that was without prey. Most interesting of all, McMillan (1975)
made detailed notes on an unidentified species of Desmometopa closely associated
with spiders in Western Australia, and called by him "cleaning flies" because of
their habits. They not only congregated in numbers on the spiders’ prey (bees and
cicadas) but also on the spiders themselves. These had become "wet and sticky
around their chelicerae and mouths" from feeding on the bees, and the flies were
observed “actually feeding ... actively all over the bases, fangs and mouth.”
McMillan noted that none of the spiders observed attempted to capture or rid
themselves of the flies and in fact seemed "to actively cooperate with them in
making the cleaning easier by opening their chelicerae.”
There may be other instances in the literature, but I have not attempted an
exhaustive search for present purposes. I can add seven records from material
that I have identified:
D. floridensis n. sp.: Lake Worth, Fla., “on asilid prey” (S.W. Bromley).
10 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
D. m-nigrum: San Diego, Calif., “feeding at Apis wrapped up by Metargiope
spider" (F.X. Williams); Maadi, near Cairo, Egypt, numerous (ca. 75) on a honey
bee captured by a spider, Thomisus sp., "hovering in a cluster very closely over
bee thorax and sometimes crawling or resting briefly on it, as if to obtain a fluid”
(Harry Hoogstraal).
D. sordida: France, “Sur Abeille captura par WHarpactor" (Hemiptera,
Reduviidae) (H. Manwal); England, with two honeybees labeled "sucked by
Desmometopa (L. Parmenter).
D. tarsalis: Jamaica, “flies which attack a large spider Nephila clavipes
(H.G. Hubbard); Panama, Canal Zone, “pentatomid” (Michael Robinson).
Biology of the Larvae
Rearing records of Desmometopa show feeding on a wide variety of spoiled,
decaying, or rotten plant material, with rare exceptions. Specimens have been
personally identified or verified except as noted.
From manure, dung, and sewage:
lO
. inaurata: poultry: Hawaii (Y. Tanada), Samoa (P.A. Buxton, G. H. Hopkins),
Nyasaland (i.e., Malawi) (W.A. Lamborn).
horse: Samoa (Buxton and Hopkins).
“manure”: Guyana (F.A. Squire).
.m-nigrum: chicken: Auburn, Ala., and Montgomery Co., Va. (G. Breeden).
. singaporensis: cattle: Pakistan (L.S. Sohi), Guam (Bohart and Gressitt
1951, as "tarsalis,” “in moist cattle excrement, both fresh droppings and when
piled as manure.”).
poultry: Hawaii (J.F. Illingworth, Y. Tanada), Samoa (Buxton and Hopkins).
. sordida: cow: Dallas, Tex. (F.C. Pratt).
. tarsalis: cow: Guam (J.L. Gressitt).
. Varipalpis: in sewage water: Dade Co., Fla. (J. Porter); in septic tank:
Khartoum, Sudan (H.W. Bedford); “breeding in traps of sinks”: Brookings, S.
Dak. (H. C. Severin); “millions...breeding on the bio-filters” in “trickle
sewage filter": Lafayette, Ind. (G.L. Walker); “eri dung" (i.e., feces of
Attacus sp., probably A. ricini, a wild silkworm): Coimbatore, South India (Y.
Rao).
. sp.: from stable manure and from toilet pools: Sendai, Japan (Kato and
Hori 1952; unverified).
|O|O
IO|O|O
lO
From plant material:
. gressitti: “ex papaya log": Truk (R.W.L. Potts).
. inaurata: “from pods of Inga ingoides infested with olethreutid and
cosmopterygid larvae": Dominica (J.F.G. Clarke); “from larvae feeding on
rotten cow pea seed": Fiji (W. Greenwood); “from over-ripe coffee
cherries": Kenya (1.3. Anderson); "ex maize cob": Sierra Leone (E.
Hargreaves); “ex avocado pear fruit": Sierra leone (E. Hargreaves): “bred
from decaying banana skins": Uganda (E.G. Gibbins).
lettuce": N. Nigeria (J.C. Deeming); “bred from decaying banana skins”:
Uganda (E.G. Gibbins).
. magnicornis: “reared cacao pods": Ibadan, Nigeria (R.W. Williams).
. melanderi: reared from Opuntia cacti: San Dimas Canyon, Los Angeles Co.,
Calif. (C.P. Christianson, J.P. Fonseca).
lIOJO!O
lO
IO!O
lO
Oo fm © |[O
JOJO
|[O
lO
Sabrosky: Desmometopa of the World 1}
. meridionalis: "ex rotting Jack fruit": Bahia, Brazil (J.A. Winder).
. nearctica: “reared from grass”: Coachella, Calif. (D.G. Hall, Sr.).
. saguaro: “ex rotting Saguaro”: Pima Co., Ariz. (F.J. Santana); reared
from Opuntia cacti: San Dimas Canyon, Los Angeles Co., Calif. (R.E.
Ryckman).
. singaporensis: "from rotten onions” and "from rotten pawpaw stem”:
Darwin, N.Terr., Australia (G.F. Hill); “from onions imported from
Australia": Fiji (H.W. Simmonds); “decaying stump of a papaya tree": Guam,
as “tarsalis” (Bohart and Gressitt 1951); “ex Pomalo fruit": Malaya (G.H.
Corbett); “larvae feeding on decaying inflorescence of Areca catechu":
Malaya (G.H. Corbett); "ex decaying leaves of Brassica oleracea": Malaya;
"ex rotten Solanum tuberosum": Malaya; "bred from decaying banana skins":
Uganda (E.G. Gibbins).
. sordida: “reared from grass silage": East Lansing, Mich.
. tarsalis: “reared from decaying Cereus gigantea": Wickenburg, Ariz. (R.E.
Ryckman and C.T. Ames)(Ryckman and Ames 1953); “reared in pond weed":
Guam (G.E. Bohart and J.L. Gressitt); “emerged from decaying barrel
cactus”: Jamaica (E.F. Legner).
. Varipalpis: “reared ex rotting Saguaro": Pima Co., Ariz. (F.J. Santana);
“reared from decaying head lettuce": Coachella, Calif. (D.G. Hall, Sr.);
"larvae in potatoes": New York City, N.Y. (in ship from Argentina): "ex
potatoes”: Algiers, Algeria; “frf[om] blue figs": Jerusalem, Israel (J.H. Brair);
"reared ex damaged sugar beet roots": Khorassan, Iran (Mir Salavatian):
“from decaying melons": Khartoum, Sudan (R. Cottam); "ex rotting potato”:
Kinshasa, Zaire (M. Wanson); “from rotting mustard stem": Coimbatore, South
India; "from rotting pomegranate": Coimbatore, South India; “from larvae on
rotting pumpkin": Coimbatore, South India (Fletcher).
. sp. (woldai?): “reared from Pachycereus pringlei”: Baja Calif., Mexico
(R.E. Ryckman et al.).
.sp.: “ex rotting Jack fruit": Bahia, Brazil (J.A. Winder).
Miscellaneous food media
. inaurata: “ex locust eggs": Zimbabwe (A. Cuthbertson); rotting snails and
Drosophila pupa: Hawaii (Hardy and Delfinado 1980).
. leptometopoides: “reared from mud and debris collected from pools": Accra,
Ghana (J.W. Scott Macfie).
. M=-nigrum (not checked; probably tarsalis): “reared from water contained in
the axils of the large bracts of decaying Heliconia blossoms": Hawaii
(Swezey 1952).
. singaporensis: "from dead cat": Samoa (P.A. Buxton and G.H. Hopkins).
. tarsalis (unverified): “breeding in material, possibly bone meal with
molasses added, set out for cattle to lick": Oahu, Hawaii Eee
Gressitt)(Gressitt 1956).
. varipalpis: “in cadelle culture": Montreal, Canada; ‘found living around and
depositing their eggs on a fungus growing on formerly preserved and dried
sheep hearts’: Commerce, Texas (E.C. Hancock); ‘found breeding in
enormous numbers in a vermiculite-alfalfa meal-brewers’ yeast mixture used
as a breeding medium for eye gnats, Hippelates flies’: Riverside, Calif.
(Mulla and Barnes 1957).
. sp. H: “des galeries du Cossus": Algeria (P. Lesne).
12 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Sources of Material
For convenience of reference, museums and collections are referred to by the
name of the city, enclosed in brackets. I am indebted for specimens and
assistance to the individuals named.
Amsterdam: Zoologisch Museum (G. Kruseman, Jr.).
Austin (Texas): M.R. Wheeler personal collection.
Berkeley: University of California, Dept. of Entomology (the late Paul Hurd).
Berlin: Zoologisches Museum, Museum fur Naturkunde der
Humboldt—-Universitat (H. Schumann).
Budapest: Zoological Section, Hungarian Natural History Museum (F.
Mihdlyi, L. Papp, A. Sods).
Cambridge (Mass.): Museum of Comparative Zoology, Harvard University
(N.E. Woodley).
Colombo: Dept. of National Museums, Sri Lanka (through K.V. Krombein).
East Lansing (Mich.): Dept. of Entomology, Michigan State University
(repository of R.R. Dreisbach Collection)(the late R.R. Dreisbach).
Eberswalde: Institut fur Pflanzenschutzforschung, Bereich Eberswalde,
German Democratic Republic (formerly Deutsches Entomologisches Institut,
Berlin-Dahlem)(the late W. Hennig, G. Morge).
Gainesville (Fla.): Florida State Collection of Arthropods) (H.V. Weems, Jr.).
Helsinki: Zoological Museum, University of Helsinki, Finland (B. Lindeberg,
W. Hackman).
Honolulu: Bernice P. Bishop Museum (the late J.L. Gressitt, N. Evenhuis).
lansing (Mich.): W.L. Downes personal collection.
Logan (Utah): Dept. of Entomology, Utah State University (W.J. Hanson).
Loma Linda (Calif.): College of Medical Evangelists (R.E. Ryckman).
London: Dept. of Entomology, British Museum (Nat. Hist.) (B. Cogan),
including material from the Commonwealth Institute of Entomology (the late F.
van Emden).
Ludwigsburg: Staatl. Museum fiir Naturkunde in Stuttgart, Zweigstelle
Ludwigsburg, West Germany (B. Herting).
lund: Museum of Zoology, University of Lund, Sweden (H. Andersson, R.
Danielsson).
Ottawa: Canadian National Collection (J.F. McAlpine).
Paris; Museum National d'Histoire Naturelle, Entomologie (L. Matile, L.
Tsacas).
San Francisco: California Academy of Sciences (P.H. Arnaud, Jr.).
Stockholm: Naturhistoriska Riksmuseum, Entomologiska Avdelningen (R.
Malaise).
Sydney: School of Public Health and Tropical Medicine, University of Sydney,
Australia.
Tucson: Dept. of Entomology, University of Arizona (F.J. Santana).
Tucuman: Instituto Miguel Lillo, Tucum&n, Argentina (the late M. Aczél).
Vienna: Naturhistorisches Museum Wien (Ruth Contreras—Lichtenberg).
Washington (D.C.): U.S. National Museum of Natural History (including
material from Henk Wolda, Smithsonian Tropical Research Institute, Balboa,
Panama).
Acknowledgments
In the preceding list of "Sources of Material", I have indicated my
indebtedness to: numerous museums, curators, and individuals for the loan of
material or the study of specimens in their collections. Beyond this, however,
Sabrosky: Desmometopa of the World 13
special thanks are due to individuals who loaned holotypes or entire type series, in
some cases waiting for years more or less patiently while my understanding of
some difficult complexes was evolving. Having all these types before me
simultaneously was of enormous advantage. I acknowledge with deep gratitude
the cooperation of B. Herting (Ludwigsburg), G. Kruseman, Jr. (Amsterdam), F.
Mih4élyi (Budapest), G. Morge (Eberswalde), H. Schumann (Berlin), A. Sods
(Budapest), and N.E. Woodley (Cambridge). Figures 1-3, 5-11, and 14 were drawn
by Kathryn M. Conway, and the author's figures were completed and the plates
arranged by Linda Lawrence.
Desmometopa Loew
Desmometopa Loew, 1866, Berlin.Ent.Ztschr. (1865) 9: 184 (Cent. 6, no. 96).
Two species. Type species, Agromyza m-atrum Meigen, 1830, by designation
of Hendel, 1903, Wien. Ent. Ztg. 22: 251, = D. sordida (Fallén).
Platophrymyia Williston, 1896, Trans. Entomol. Soc. London 1896: 426. Type
species, P. nigra Williston, 1896, by monotypy. (Synonymy by Sabrosky, 1973).
- Desmetopa (error) Hendel, 1902, Wien. Ent. Ztg. 21: 262-4.
Liodesmometopa and Liodesma Duda, 1935, Natuurhist. Maanblad 24: 24, 25.
Subgenus of Desmometopa. Type species, D. atra Duda, 1935, by original
designation, = D. sordida (Fallén)(Synonymy queried by Hennig 1937,
confirmed here).
There is great uniformity of color, structure, chaetotaxy, and general habitus
among the species of this genus, and the characters given here are usually not
mentioned further in the individual descriptions.
Small flies (1-2.5 mm), black in ground color, sometimes entirely so, some
species with yellow to orange-yellow color on antennae, palpi, propleura, halter
knobs, fore coxae, and tarsi, especially mid and hind tarsi.
Frons with black M-shaped frontal vitta delineated by the frontal triangle
and the fronto-orbital and interfrontal plates (e.g., figs. 1,2,10); each
fronto-orbital plate with 2 lateroclinate upper orbital and 2 mesoclinate lower
orbital bristles; inner and outer vertical, ocellar, and postocellar bristles strong; a
row of 4 to 6 short setae on each interfrontal plate. Eye large. Cheek usually
narrow, 1/3-1/2 the breadth of a 3rd antennal segment, but broad in a few species
like D. m-nigrum. Postorbital and postgenal areas usually narrow. Distinct lunule
projecting between bases of antennae. Face with more or less distinct median
carina, and oral margin warped forward and upward, leaving subcircular and
concave antennal grooves (foveae). Vibrissal angle either strongly produced
forward to about a 45° angle (fig. 18), with face decidedly concave in profile
(subgenus Platophrymyia), or not so produced, the angle about 80° to 90° and face
not or weakly concave in profile (figs. 6-8) (subgenus Desmometopa). Palpus
usually moderately large, clavate, occasionally broad and flat (fig. 4), and even
capitate or elongate fusiform in males of species showing sexual dimorphism (figs.
3,5). Proboscis commonly slender, geniculate, haustellum often as long or longer
than lower margin of head, labella usually as long as haustellum or nearly so.
Antenna usually small, 3rd segment only a little larger than 2nd segment; arista
slender, micropubescent.
Thorax black, subshining dorsally, densely microtomentose, usually gray to
brownish gray, brighter gray on pleuron, the pleuron occasionally entirely gray
microtomentose (four species) but in most species with some bare and polished
areas (figs. 23-27), in a few species almost entirely polished. Chaetotaxy: 1
humeral, 1 + 1 notopleural, 1 presutural, 1 postalar, 1 dorsocentral, 2 scutellar, |
small propleural, and 1 sternopleural pairs of strong bristles; a 2nd short
14 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
- dorsocentral anterior to but close to the strong dorsocentral and usually not
conspicuous; prescutellar, supra-alar, and intra-alar bristles are much weaker and
usually not noticeable but may sometimes be developed. Mesonotum densely
haired but scutellum bare; pleuron predominantly bare, only the sternopleuron
with some hairs.
Legs usually slender and without striking characteristics except for a few
species with fore coxa elongate in males, and sometimes fore femur as well,
raptorial in appearance (e.g., fig. 22).
Wing venation differing little throughout the genus (cf. Curran, 1934, p. 337,
fig. 16; Hennig, 1937, fig. 36), the 2nd vein and 2nd sector of costa very long, 2nd,
3rd, and 4th veins ending near apex of wing, and usually the 3rd and 4th veins
slightly convergent toward apex of wing; costa extending to 4th vein (M), with
both humeral and subcostal breaks, the costa between the breaks with up to 16
erect to semi-erect dorsal setae, usually fine but in a few species (ciliata, etc.)
coarse and well spaced.
KEY TO THE WORLD SPECIES OF Desmometopa
(For cautionary remarks on interpreting some characters, see the
introductory section on “Morphological Characteristics." Bracketed characters
may be useful, in addition to regular parts of a couplet. This key is followed by a
"Key to males with unusual characteristics.”)
l. Pleuron of thorax entirely gray microtomentose [Note: If thinly so, as in
lucidifrons, Concave areas such as anterior slope of sternopleuron will be
shining and the microtomentum difficult to see]. ...... 2... ee eee eee 2.
—- Pleuron with polished black spot posterodorsad to fore coxa, entirely or
chiefly on anterior slope of sternopleuron, in a few species pleuron
extensively pOlshed 6s ee Oe ee errr ee eS 5.
2. Cheek with broad polished subocular crescent that is 2/5 height of cheek,
extending as broad band along entire lower margin of eye (fig. 15); [all tarsi
yellowish except distally] (Gambia, Nigeria)........ 1. D. pleuralis, n. sp.
-- Not so, cheek with narrower subocular crescent that is either linear or
wicened anteriorly (figs. 14; 20). 3 oe ee ee 3.
3. Entire frons dull, heavily gray to brownish gray microtomentose, viewed from
most angles the interfrontal and fronto-orbital plates only weakly
demarcated; lunule yellow, large and long, extending to or beyond apices of
2nd antennal segments (Nigeria)................- 2. D. nigeriae, n. sp.
~- Not so, frontal vitta entirely or chiefly subshining velvet black, at least
frontal triangle and fronto-orbital plates sharply demarcated; lunule
blackish, small, shorter than preceding... ee ee se eS 4.
4. Mesonotum bright gray microtomentose with yellowish to golden cast; all
tarsi infuscated: subocular crescent linear (fig. 14); frons with M-shaped
frontal vitta subshining velvet black, interfrontal plates strong and distinct
(Wisespread) i ee ee ee re es 3. D. inaurata Lamb
--- Mesonotum dark gray to brownish gray microtomentose; mid and hind tarsi
yellow except distal tarsomere or two; subocular crescent widened
anteriorly (fig. 20); frons with anterior 2/5 glistening, interfrontal plates
weak and obscure, evanescent (Trinidad)......... 4. D. lucidifrons, n. sp.
Sabrosky: Desmometopa of the World 15
5.* Cheek exceptionally broad for Desmometopa, appearing equal to breadth of
3rd antennal segment or nearly so and often with broad and triangular
polished subocular crescent (fig. 7), or postgenal area broad (fig. 17), or
both, postorbital area also broad in males of two species............ 6.
*([Note: A possible new species from Algeria, sp. H, tentatively associated
with the broad-cheeked species, is represented by two teneral males and
may not belong here. It has a narrow subocular crescent and somewhat
broad and flat palpus (cf. fig. 4). If it should prove to have the cheek
obviously narrower than 3rd antennal segment, it would pass to couplet 43,
but it agrees with neither of the species there.]
Cheek not so, much narrower and obviously less than breadth of 3rd antennal
segment, any shining subocular crescent usually linear (figs. 3,5,11), broad
in only a few species; postgenal and postorbital areas always narrow . . .10.
Thoracic pleuron chiefly polished, including entire propleuron and area almost
surrounding anterior spiracle (fig. 28) (Texas, Calif.).................
sia a le Gm eeeeel C6 ek We es es Os 5. D. latigena, n. sp.
Thoracic pleuron predominantly dull, gray microtomentose, including entire
propleuron and area surrounding anterior spiracle.................. i.
Palpus yellow on basal third to half or more, slender clavate in both sexes,
gradually broadening from base. to apex .... 6.6.66. Ski ves eee e's 8.
Palpus black, somewhat broad and flat distally in male (not as extreme as fig.
4); [halter brown; polished spot on pleuron bilobed] (Algeria, 2 males). ....
Ro a SIG ae aera ak GS ae a lis ee a wh ee ge oi 6. D. sp. H
Polished spot on pleuron relatively large, bilobed, the dorsal lobe an
elongate-oval anteroventral area of mesopleuron (fig. 23); knob of halter
VOOM ii icicinn ul Rinna dy Winellie Suen reel le Bie Mowe le a ich dgrigs Ode F
Polished spot on pleuron relatively small, not bilobed, not with adjoining
polished area on mesopleuron; knob of halter brownish; [postgenal area
wide in both sexes, and in male the postorbital area broad to vertex, both
areas convex and bulging (fig. 17)}] (Afrotropical and Oriental Regions, to
CI) owt ek a ae ed a es re es 7. DO. microps Lamb
Postorbital and postgenal areas in male exceptionally broad, shining black,
the former fairly broad up to vertical bristles, the latter continued forward
nearly to vibrissa as a band nearly half as broad as cheek (fig. 13), in
female the band distinct but postorbital and postgenal areas narrower
(ere MICS A) 6. 5 hide a uw ees we at iroute fi 8. D. postorbitalis, n. sp.
Postgenal area only slightly broadened and not continued forward as a broad
band, the subocular shining area triangular, the postorbit narrowed dorsally
(fig. 7) (widespread, especially Holarctic Region).......... Brie cae eet
ian Cay wien. Seen Meuecietiel CieGad oe hte iN abi day Gi gel ing War yy 9. D. m-nigrum (Zett.)
Each fronto-orbital and interfrontal plate wide, and frontal triangle long,
hence the black M of frontal vitta with exceptionally narrow sections, at
least inner ones little over half as wide as an interfrontal plate (fig. 10)
CPT ROM TaN le cbt gi carl iets aig Mic aaa 10. D. interfrontalis Sabr.
Each fronto-orbital and interfrontal plate narrower and frontal triangle
shorter, the black M of frontal vitta more conspicuous (except in
obscurifrons), each section almost always equal to or wider than a plate. .
ey ae UNA oa tty ima: a lt a aly a Ek SIN ge gia iN atic agate) Lh
Fore coxa yellow or predominantly so, contrasting with black thorax, often
elongate in male but not or only slightly elongate in female; [vibrissal
angle strongly produced, to a 45° angle] (flavicoxa group of subgenus
PLAC OO ABO ROOIOR GOD yaks bb ck kd Kalk ee Ce k ee 2.
FOre Coxe entirely eG Or DYOWII@ DINO. 6 ok ak ec kde ck ek nwa ere 23.
13.
Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
. Pleuron chiefly bright gray microtomentose with large polished black spot
- posterodorsad to fore coxa and including the adjoining anteroventral area
of mesopleuron (as in fig. 24); propleuron and areas surrounding anterior
spiracle entirely and heavily gray microtomentose, and mesopleuron
predominantly so; propleuron black in ground color.............-- 13.
Pleuron chiefly, sometimes almost entirely, polished black (cf. fig. 27),
including propleuron (at least ventrally), or areas surrounding anterior
spiracle, or both, and mesopleuron entirely or chiefly; propleuron
orange-yellow in some Species... 2... cee eee eee er eee e ee eees 16.
Interfrontal plates notably short, narrow and evanescent, each appearing to
consist of 2 to several small, separate microtomentose spots surrounding
bases of interfrontal setae (Panama)........... 11. D. evanescens, n. sp.
Not so, plates distinct, if short the frons approximately square......... 14.
Frons clearly longer than broad (about 1.25x), entirely black.......... rs.
Frons relatively broad, approximately square, at least in female (male
unknown), narrowly yellow along anterior margin (s. Brazil), 1 female)... .
Pe OE Pe a a es eee BEE ee eG ee 12. D. sp. I
. Male: Palpus entirely black (Neotropical)............ 13. D. woldai, n. sp.
[See woldai for possible species that key here]
Male: Palpus orange-yellow on more than basal half (Argentina).........
Oe Wd ee ee ey in Ore RE aS 14. D. flavicoxa Hendel
[Note: The holotype of flavicoxa, a female, has black palpi, but the male
could be either black or orange-yellow. I have assumed the latter, from an
available male from Argentina. Thus far I cannot separate or satisfactorily
associate females of woldai and flavicoxa.]
Frontal vitta shining or subshining velvet-black, viewed at any angle..... Ly.
Frontal vitta changeable, velvet-black at some angles, but at others the
anterior 2/5 dull brownish gray like frontal triangle; [pleuron almost
entirely polished anterior to pleural suture; propleuron orange-yellow;
halter knob yellow; all tarsi black] (Panama; 1 male)......... 1. D.. sp. J
Knob of halter yellow or whitish yellow. ... 2... cece cere er eevrcees 18.
Knob of halter brown-black, concolorous with stalk; [pleuron chiefly polished,
mesopleuron entirely so] (Argentina)........ 16. D. nigrohalteralis, n. sp.
. Small area behind anterior spiracle gray, microtomentose, sometimes
continuous with broad or narrow band of microtomentum along dorsal and
posterior margins of mesopleuron (fig. 27)... 6. eee cee eee ee ee eee ee
Postspiracular area polished, as is mesopleuron almost entirely......... 21.
Palpus yellow on basal half or more, gently clavate in both sexes; propleuron
Black or GhlOhly SOc Se OP ee oe ee 20.
Palpus entirely black in male (female unknown), broad and flat (cf. fig. 4);
propleuron orange-yellow (s. Brazil, | male).............. 17. DO. sp. K
. Mesopleuron chiefly polished black, sometimes appearing entirelyso, but
postspiracular depression always with small patch of gray microtomentum
and usually a narrow band of same along posterior margin of mesopleuron
(fig. 27), occasionally the two narrowly connected along dorsal margin
(Belize, Mexico, Panama). ...... 0.0. e cee eees 18. D. glaucanota, n. sp.
Mesopleuron with a broad band of gray microtomentum dorsally and
posteriorly that extends across anterior spiracle and propleuron (cf. fig. 26)
(Plorida, Georges TP a ree es 19. D. floridensis, n. sp.
wily
Ze.
24.
28.
"7.
_ —
Sabrosky: Desmometopa of the World i?
Frons shining black; interfrontal plates without microtomentum, shining, only
weakly distinguished from the shining frons; antennal fovea thinly
microtomentose and rather shining; pteropleuron chiefly polished, at least
on lower half; [male with palpus broad and flat (cf. fig. 4)] (3 males, Peru
and Costa Rica, have orange-yellow propleuron; 2 females, Colombia and
Ecuador, have propleuron black). ............0-- 20. D. indistincta, n. sp.
Frontal vitta subshining, velvet black; interfrontal plates microtomentose,
well marked against velvet black vitta; antennal fovea densely bright gray
microtomentose; pteropleuron entirely gray microtomentose......... ake
Male with propleuron strikingly orange-yellow and palpus broad and flat (cf.
fig. 4); female apparently distinguishable only by geographic distribution
and association with male (Argentina, Brazil, Uruguay, Bolivia, Peru) ....
EES EES OPS PORE Fe ee Oe OR Tae 21. D. meridionalis, n. sp.
Male with propleuron black and palpus clavate; female as noted in preceding
(MGKIGO TO FaNeMminy. Br Se Seis Pa Oa’ abe 22. D. blantoni, n. sp.
Aidomen encirely GiaCKke Ue ON a RE Ee NS SPO 24.
In male, margin of 4th tergum, all of 5th, and all terminalia orange-yellow;
female unknown but assumed to show some color at apex of abdomen
CPOE TS re CPP? OP ERE aes 23. D. terminalis, n. sp.
Thoracic pleuron predominantly dull or subshining, gray microtomentose,
including entire propleuron and area surrounding anterior spiracle (cf. fig.
QO EL PRE DE POR i EEE BE POTS CRE TT Fee ees 25.
Propleuron chiefly polished black (fig. 26), rest of thoracic pleuron anterior
to pleural suture usually predominantly so...........22 cece eee 47.
Frontal vitta dull and gray to brownish gray, viewed at most angles,
interfrontal plates only weakly contrasting............e.-ee2000. 26.
Frontal vitta subshining, velvet black, the gray interfrontal plates sharply
distinct, or Trone shining GN QNCSPIOL OTe ee ate ee BE ee 28.
Lunule, antenna, palpus chiefly, and proboscis black ................ ag
Lunule, antenna in part, palpus chiefly, and proboscis yellow (Neotropical)
Deh Cita kg a tea ke eta A TRE he Ne le ee es 24. D. obscurifrons, n. sp.
Epistomal margin and lateroventral corner of facial plate strongly warped
forward well in advance of and accentuating the vibrissal angle (cf. fig.
18); [male with fore coxa and fore femur elongate] (Texas, Mexico)......
EE Ge ae Oae OW he ee OE Ware ed eek 25. D. parafacialis, n. sp.
Epistomal margin and lateroventral corner of facial plate only weakly warped
forward, the vibrissal angle about a 70° angle (fig. 12); parafacial midway
not or only linearly visible in profile; cheek with comparatively broad
polished subocular crescent, half as broad as cheek; [male unknown but
probably fore coxa and fore femur not elongate] (Panama, Ecuador, Peru; 2
females, s. Brazil and Trinidad, key here and may be conspecific).......
STAM SIDA AINE AURA Mee. fi orgs NEM QUENT att gir Anna Pp eee: aa rar gi 26. D. atypica, n. sp.
Vibrissal angle not produced anteriorly, the angle 80° to 90° (figs. 3,5,11),
face only weakly concave in profile; lateroventral corner of facial plate
dull gray like rest of face, and not warped forward............e6-. 29.
Vibrissal angle produced anteriorly to about a 45° angle (cf. fig. 18), face
deeply concave in profile, emphasized by shining black lateroventral corner
of facial plate, mesad of vibrissal angle, which is warped forward often
DOYONG ViDPIeOet EI ii eT OE OOS S Gh VAC De 8 ARO 46.
Cn OF EE RE Og ne ee A ale bl ere ord. bee Oks 30.
NOD OT MM TORP ety CO LA ee Ne Oe EA See 36.
30.
34.
35.
Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
[*Note: Teneral specimens or those mounted out of fluid may be pale, and
caution must be exercised. Species with brown to blackish halteres usually
retain at least a brownish tint, however, even though the paleness suggests
otherwise. The marginal specimens are all in the tiny species, 1.25-1.5
mm, whereas most of the species with yellow halteres are larger, 2.2-2.5
mm, and considerably bulkier. ]
Polished spot on thoracic pleuron, posterodorsad to fore coxa, relatively
large, including elongate-oval area along anteroventral margin of
mesopleuron (fig. 24); 2nd subgenal seta behind vibrissa developed as a
strong bristle, subequal to vibrissa (fig. 11) (Australia)................
Polished spot on thoracic pleuron relatively small, confined to anterior slope
of sternopleuron, the mesopleuron not polished anteroventrally (fig. 25); no
outstanding subgenal bristle subequal to vibrissa, although in one species
(leptometopoides) the subgenal setae quite long and becoming longer
toward vibrissa, and the second may be stronger than the others....... 51.
WAGNCS ioe oe Ba rs Bw a eee A re wes 32
PRG pci ok eek ie a re eo i es hae se oe ws i 34.
Hind tibia unusually broad and flat, resembling that of Leptometopa (fig. 19);
palpus clavate, gradually enlarged distally (West Africa; ? Cape Province) .
PRS io eee ae Bae ee 28. (male) D. leptometopoides, n. sp.
Hind tibia slender; palpus elongate and greatly broadened distally (figs. 3 ae
Palpus fusiform elongate, often considerably so, tapering to acutely ae
apex (fig. 3); cheek wider than in singaporensis (cf. figs. 3,5) (widespread) .
gh ieee wee we oe ee es ee a 29. (male) D. varipalpis Mall.
Palpus capitate, uy broadened, rounded distally (fig. 5); cheek narrower
than in varipalpis (cf. figs. 3,5) (widespread)..............
sos cue 4. a ly au tik Rak eln Ras ye ds ese 30. (male) D. singaporensis 5 Kert.
ec Se es i ns (syns.: D. tristicula Hendel, D. palpalis Meij.)
Cheek comparatively narrow, usually barely over 1/10 the height of an eye
(cf. fig. 5 of male); each fronto-orbital plate not appearing broad, lower
section in particular approximately equal to that of an interfrontal plate
Cheek obviously broader, about 1/5 height of eye (fig. 3), each fronto- orbital
plate relatively broad, obviously greater than breadth of an interfrontal
plate (fig. 1)(widespread)...........2026- 29.(female) D. varipalpis Mall.
Cheek black in ground color, heavily gray microtomentose; frontal triangle
large and interfrontal and fronto-orbital plates relatively broad, the
sections of black M of frontal vitta relatively narrow, posterior arms of
interfrontal plates separated from frontal triangle by approximately their
own width (West Africa; ?Cape Province) ...... 2. ee cc ence enc cc ncas
se Sey cater © CP ak i ei ie ec a ae 28. (female). D. leptometopoides, n. sp.
Cheek yellowish in ground color, thinly microtomentose; sections of black
M-shaped frontal vitta relatively broad (fig. 2), interfrontal plates usually
more widely separated from frontal triangle, by twice their own width
(WIGESOTE OG). odie ekerce le wba Wee eeadanee 30. (female) D. singaporensis Kert.
ne Regn aren yee eee ree (syns.: D. tristicula Hendel, D. palpalis Meij.)
Subocular crescent narrow, linear to sublinear (cf. figs. 5,14);chiefly tiny
BOeCIOS 17a Ie ae ee ie ke ee ee Sy Gace as es ee ee eh,
Subocular crescent broadened behind vibrissa, subtriangular (fig. 8); relatively
large and bulky species, 2-2.5 mm (Holarctic)...... 31. D. sordida (Fallén)
oye
4].
48.
Sabrosky: Desmometopa of the World 19
Frontal triangle and ocellar tubercle virtually coextensive, the gray
microtomentum of triangle barely or not at all extending anterior to
Miediat’ OCEIIUS ee eS a See PSE Re Oe es 38.
Frontal triangle longer, extending into median part of frontal vitta...... 42.
Palpus black in GOth Sexes Pie ee Fe ee we ee wee es oes 59.
Palpus partly orange-yellow, at least on basal third to half............ 40.
Third antennal segment of male relatively small, little larger than 2nd
segment; costa between humeral and subcostal breaks with only 5 erect,
well-spaced setae (Malaya, 1 male)...........2. ccc eeees a2: 0 She
Third antennal segment of male exceptionally large (as in fig. 21); costa
between breaks with 7-8 dorsal setae (West Africa)................
At least mid and hind tarsi yellow except distally................6.- .
All tarsi black (Marshall and Palau Is., New Hebrides; ?Philippines)........
PEER ES OS OEE CPOE Er CET OCR 34. D. flavipalpis, n. sp.
Palpus heavily infuscated distally and below in both sexes; antenna black in
both sexes; polished pleural spot bilobed anteriorly sie fig. 23)(Sri Lanka;
PPO IIGS): 4 6 KO ae Ge OR EEE PETS 35. D. srilankae, n. sp.
Palpus chiefly yellow in male, sometimes infuscated at tip, i in female heavily
infuscated distally; antenna black in female, 3rd segment orange-yellow on
basoventral half in male; polished pleural spot not bilobed anteriorly
(Malaya, Jave, (nellang): 3. yh e oN 36. D. propeciliata, n. sp.
At least mid and hind tarsi yellow except distally..................- 43.
All tarsi infuscated (Nigeria, Ivory Coast)........ 37. D. magnicornis, n. sp.
. Second subgenal seta behind vibrissa developed as a strong bristle, standing
out among the shorter setae in subgenal row (cf. fig. 11)............ 44.
Subgenal setae even, none developed as an outstanding bristle although setae
may lengthen gradually toward vibrissa: ee ee a ee ee eee 45.
. Polished subocular crescent distinct, i hl linear; male unknown (Taiwan,
PPO eo eee NEE OT CECE eee Ree Os 38. D.sp.M
Subocular crescent absent or indistinct; 3rd antennal segment of male
exceptionally larae (cf: fig. 21) (Philippine Is.) 2 oe es we we ee
CE ne Sa EN ad Fre ee a ee ee ae ey ae 2 ee philippinensis, n. sp.
Polished subocular crescent distinct, although linear; palpus black in female
(male unknown) (Malaya; Philippines)..............22-00. 40. D. sp. N
Subocular crescent absent or indistinct; palpus yellow in both sexes, slightly
infuscated at apex (Aldabra).............2-e000- 41. D. aldabrae, n. sp.
Polished pleural spot small, not including any area of mesopleuron (cf. fig.
25); palpus ordinary, gently clavate; abdominal tergum 5 of male elongate,
longer than terga 3 and 4 combined (Sri Lanka) . . .42. D. kandyensis, n. sp.
Polished pleural spot relatively large, including anteroventral area of
mesopleuron (as in fig. 24); palpus of male especially broad and flat (fig. 4);
abdominal tergum 5 of male not elongate, barely longer than tergum 4
(South Pacific: Caroline, Gilbert, and Marshall Islands, Guadalcanal, New
PIOMTICee) ee ee Bi ee Oe bee be EES 43. D. gressitti, n. sp.
Mesopleuron microtomentose dorsally and posteriorly, the dorsal band
extending to anterior spiracle, though sometimes narrowly (as in fig. 26)..
Mesopleuron extensively polished black, the immediately postspiracular area
OCT TGTVCE Ce NSE 155 a ke eR ea ek ate SE wo Saree a ah
Frons dull gray from most angles of view, the interfrontal plates obscure . .
Not so, frontal vitta subshining velvet black, interfrontal plates well
COMCPARLOO le aN a ee ae ee ee ee CL CHEN Wh bala cee ge tts 50.
20
49.
Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Fore leg of male raptorial in appearance, mantislike, the fore coxa and femur
elongate, latter obviously longer than other femora and with anteroventral
and posteroventral rows of short, even, straight spinelike bristles (fig. 22);
fore coxa and femur of female longer than usual, coxa more or less
elongate but not as extreme as in male; [wing whitish, veins whitish yellow]
CoG Re PI) catia. woe beech tae anew rk ens 44, D. saquaro, n. sp.
Not so, fore coxa and fore femur not elongate (circum—Caribbean, also
Mawel to Solomon Isignads) i sis cnc. Siseieacs Suse ewes os 45. D. tarsalis Loew
. Subocular crescent relatively broad, obviously over 1/2 breadth of cheek,
broad anteriorly, similar to fig. 20 but usually not triangular; Nearctic
(Calif. to Utah and Texas, N.Y..to. Kans..and.Ga.).: ...c gic. ieee OS
Said Den ra ee ars Fe es TS a ee OS 46. D. nearctica, n.
sp.
Subocular crescent comparatively narrow, obviously less than 1/2 breadth of
cheek [Warning: teneral specimens will appear like nearctica]; South
Temperate (Argentina; 1 Peru)...........ee00- 47. D. argentinica, n. sp.
Knob of halter lemon yellow; pteropleuron gray microtomentose; frontal vitta
a ay Nia ess ck Hin he esd os 2 Ne Os
Knob of halter black; pteropleuron polished black; frontal vitta subshining
black, extremely broad, the interfrontal plates narrow and lower
fronto-orbital plates reduced to mere lines (Mexico, l female)... 6c... 6s.
Frontal vitta dull gray—black from above and in front, with velvet black spot
along each side of ocellar tubercle ............... oe eee al 5D:
Frontal vitta chiefly subshining velvet black, thinly gray on anterior half
between and beside the interfrontal plates (s. Brazil)................
Rhee ae ewe rt mec Nererncary Her enamres ew NGC s hnpanic ra ary Macy Rs 49. D. stilbopleura, n. sp.
Fore leg of male raptorial in appearance, mantislike, with coxa and femur
elongate, fore femur obviously longer and larger than other femora and
anteroventrally with row of short, even, stout spines, posteroventrally with
row of similar but weaker spines (like fig. 22); fore coxa and femur of
female longer than usual, without spine rows, the coxa more or less
elongate though not as extreme as in male (Calif. to Texas and Mexico)...
AR Aen es os ce bce ee ants Were ete & Aces aos Ree aie 50. D. melanderi, n. sp.
Fore leg not raptorial, fore coxa and femur not elongate, without spines, fore
femur of approximately same length as other femora (Argentina). .......
Re ee Ee ee ET ee OTIC FT pu ENmPET eer hs cecavge anne 51. D. aczeli, n. sp.
Key to males with unusual characteristics
(Males, or palpi of males, unknown for atypica, evanescens,
nigeriae, stilbopleura, woldai, and spp. I, J, M, N, O)
Palpus unusually enlarged and extended (figs. 3,5), chiefly yellow........ oa
Palpus not so, either ordinary clavate, or black if broad and flat......... a,
Palpus elongate, fusiform, often considerably so, tapering to rounded but
acutely angled apex (fig. 3) (widespread)......... 29. DO. varipalpis Mall.
Palpus capitate, abruptly broadened, rounded distally (fig. 5) (widespread) .
ee a ek a ok a ue Be ae 30. D. singaporensis Kert.
Hind tibia greatly broadened, resembling Leptometopa a (fig. 19) (West Africa;
Pe Oy CG FN Wins bcc ane be een 28. D. leptometopoides, n. sp.
a SE BEET IRs ees e tv can ger er Mea gm Ur gy any ae cle unt Omer seen eM Neat at 4.
Postorbital area broadened up to vertex, postgenal area broader than usual
CPR eS ee hi hice aha i eshay Hida Lal's Sevan pene ata ual ical Bocce wm Giiaelh caus adenkile 5.
Upper portion of postorbital area narrow, linear, and postgenal area narrow
RS PORE Me eek a Ra a Te ck a ares Wide VR anne rtp ge URS a Nos tN hued 6.
Sabrosky: Desmometopa of the World 21
5. Postgenal and postorbital areas convex, appearing bulging (fig. 17); polished
spot on pleuron relatively small, not bilobed, not with adjoining polished
area on mesopleuron (cf. fig. 25); knob of halter brownish (Afrotropical and
Oriental Regions, tO Guan) iyseiises 54 b cee ew eaten ah ows 7. D. microps Lamb
-- Postgenal and postorbital areas flat, not appearing bulging; polished spot on
pleuron large, bilobed, the dorsal lobe an elongate-oval anteroventral area
of mesopleuron (cf.fig. 23); knob of halter yellow (Kenya, Uganda) (cf. fig.
23). chines aik 6 esd s sik ce Hae Se Fe are Sees 8. D. postorbitalis, n. sp.
6. Fore leg raptorial in appearance, mantislike, with fore coxa and fore femur
elongate, latter obviously longer than other femora and often more or less
inorassate (fia. 22)46 ew sree bred nee pe es 50. D. melanderi, n. sp.
21. D. meridionalis, n. sp.
44. D. saquaro, n. sp.
-- Not so, fore leg not raptorial, fore coxa and fore femur not or only slightly
ClONOGIO ss caine Wd os) HACER RE a ee ew ol EEE > SF
7. Third antennal segment large (fig. 21); palpus gently clavate............
33. D. nudigena, n. sp.
39. D. philippinensis, n. sp.
-- Third antennal segment small; palpus broad and flat (fig. 4)..............
5 A deca nieecad oh whan be ache 0 akc wal aL A ate ath wie ie Ae rh eel ee ate 43. gressitti,
20. indistincta, 50. melanderi, 21. meridionalis, 25. parafacialis, 44.
saguaro, 17. sp. K)
1. Desmometopa pleuralis, n. sp.
Sa NA
(Fig. 15)
Pleuron entirely dull gray microtomentose; cheek relatively broad (fig. 15).
Male, female. Chiefly black; palpus entirely yellow in both sexes; knob of
halter yellowish; all tarsi yellowish; distal 1 or 2 tarsomeres infuscated on mid and
hind tarsi, and distal 3 on fore tarsus.
Frons with M-shaped frontal vitta subshining velvet black, the gray
interfrontal and fronto-orbital plates and rather long frontal triangle sharply
distinct; cheek relatively broad, approximately equal to or a trifle greater than
breadth of 3rd antennal segment and 3/10 the height of an eye, with relatively
broad, shining black subocular crescent that is 2/5 breadth of cheek and continues
from slightly broader postgenal area (fig. 15); face only weakly concave in profile,
vibrissal angle rounded, about a 90° angle, approximately opposite anterior margin
of eye; a strong subgenal bristle developed, immediately below and behind
vibrissa; 3rd antennal segment small in both sexes; palpus short, gently clavate.
Thorax entirely gray microtomentose, including entire pleuron. Fore coxa
not elongate. Length, 1.5 mm.
Holotype male, GAMBIA: Bakau at Tropic Bungalow, "swept in meadow rich
in flowers, at the beach,” Nov. 7, 1977 [Lund]. Allotype female, NIGERIA: Ibadan,
Aug. 25, 1962 (D.C. Eidt; Malaise trap)[Ottawa].
This species differs from most other Desmometopa in having the pleuron
entirely dull, without a polished spot. Other species with dull pleuron have
narrower cheek and narrower subocular crescent.
The specific name is an adjective derived from the Greek pleura, side.
2. Desmometopa nigeriae, n. sp.
Frons uniformly dull, heavily brownish gray microtomentose, interfrontal and
fronto-orbital plates not strongly contrasting with frontal vitta; pleuron entirely
22 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
gray, without polished black spot.
Female (male unknown). Chiefly black, with yellow to orange-yellow lunule,
Ist and 2nd antennal segments, palpus chiefly, and proboscis; all tarsi yellow
except distal segment or 2; knob of halter yellow.
Frons uniformly dull brownish gray from most angles of view, the interfrontal
and fronto-orbital plates and frontal triangle scarcely evident, not strongly
contrasting with frontal vitta and thus not demarcating the usual black "M" of
most species of Desmometopa; interfrontal plates long, posterior ends at level of
foremost upper orbital bristles; cheek narrow, 1/3 breadth of 3rd antennal
segment and about 1/10-1/11 the height of eye, with linear subocular crescent:
face concave in profile, vibrissal angle produced to a 45° angle, accentuated by
shining black lateroventral corner of facial plate, which projects even beyond
vibrissal angle; 3rd antennal segment small, little larger than 2nd segment; palpus
large, clavate; proboscis long and slender.
Thorax entirely dull gray to brownish gray microtomentose, including entire
pleuron, with no trace of the usual shining black spot posterodorsad to fore coxa.
Fore coxa large but not especially elongate. Length, 2.5 mm.
Holotype female, NIGERIA: Olokemeji, 1914 (J.C. Bridwell) [Washington].
Paratype female, NIGERIA: Ibadan, July 4, 1962 (D.C. Eidt, Malaise trap)[Ottawa].
This species is obviously closely related to the Neotropical obscurifrons, but
it differs strikingly by having the pleuron entirely gray microtomentose and thus
the two are placed some distance apart in the key. D. nigeriae also differs in
having the 3rd antennal segment entirely black, but antennal color is probably not
significant and may be variable. The holotype has the 2nd antennal segment all
orange-yellow, but in the paratype it is blackened dorsally.
The specific name is a noun in the genitive case, from the name of the
country, Nigeria.
3. Desmometopa inaurata Lamb
(Fig. 14)
Desmometopa inauratum Lamb, 1914, Trans. Linn. Soc. l.ondon, ser. 2 (Zool.),
14: 363 (Seychelles Islands)[l.ondon].
D. ciliata sensu Malloch, 1924, Proc. Linn. Soc. N.S. Wales 49: 336 (New South
Wales); 1934, Insects of Samoa, Pt. VI (Diptera), Fasc. 8: 327 (Samoa).
D. inauratum; Lamb in Bezzi and Lamb, 1926, Trans. Entomol. Soc. London 1925:
563 (Rodriguez).
D. M-nigrum; Bezzi, 1928, Diptera Brachycera and Athericera of the Fiji
Islands [British Mus. (Nat. Hist.)], p. 163.
D. semiaurata Sabrosky, 1958, Stuttg.Beitr. Naturk. 4: 4 (Tanzania)
[Ludwigsburg]. N. syn.
D. inaurata; Sabrosky, 1958. loc. cit.: 4 (Tanzania).
D. inaurata; Hardy, 1972, Proc. Hawaiian Entomol. Soc. 21: 160 (Hawaii).
D. inaurata; Hardy and Delfinado, 1980, Insects of Hawaii, 13 (Diptera:
Cyclorrhapa III): 354-5 (Hawaii; figs. of head and male genitalia).
Pleuron entirely dull gray microtomentose; mesothorax with the bright gray
microtomentun with slightly yellowish to decidedly golden tint.
Male, female. Almost entirely black, yellowish only on antenna and palpus
(more so in male than in female), and knob of halter; antenna usually all black in
female, occasionally orange-yellow to base of 3rd antennal segment, in male base
of 3rd segment largely orange-yellow; palpus chiefly orange-yellow in both sexes,
infuscated apicoventrally, more infuscated in female than in male.
Sabrosky: Desmometopa of the World 23
Frons with M-shaped frontal vitta subshining velvet black, the fronto-orbital
and interfrontal plates, and large frontal triangle gray microtomentose and
sharply distinct; upper orbital plate much broader than lower; apex of frontal
triangle nearly midway of frons, at level of foremost upper orbital bristles; cheek
1/2 to nearly 3/5 breadth of 3rd antennal segment and 1/8-1/5 the height of an
eye, chiefly gray with linear and sometimes scarcely visible subocular crescent
(fig. 14); vibrissal angle not produced, the angle about 80° to 90° , and mesad of it
the facial plate flat and dull gray, 3rd antennal segment small in both sexes;
palpus clavate in both sexes.
Thorax entirely dull gray microtomentose, including entire pleuron;
mesonotum bright gray microtomentose, usually with distinctive yellowish to
golden tint. Fore coxa and all tarsi infuscated, the fore coxa not elongate.
Length, 2.5 mm.
The yellowish to golden tint of the mesonotal microtomentum will distinguish
inaurata at once from the other species with all gray pleuron and indeed from all
other known species of Desmometopa. Dirty or greasy specimens cannot of
course be fairly judged. The subocular crescent is narrower than in pleuralis and
_ lucidifrons (cf. figs. 14,15,20). Teneral females might be confused with females
of singaporensis, but the latter has the polished black area posterodorsad to the
After seeing much more material from a wide range of localities, I now
believe that D. semiaurata Sabrosky was based on less brightly colored variants of
inaurata. Moreover, in smaller specimens, called “semiaurata", the cheek
measures proportionately wider than in larger specimens. The subocular crescent
is normally narrow, but in some specimens, probably as a result of a slightly
teneral condition, the cheek shows a triangular folding below the polished area,
giving an appearance somewhat like that of D. m-nigrum.
Distribution: Widespread, suggesting its dissemination in commerce, but it
seems curious that I know no records from the Oriental Region. It is widespread
in the Afrotropical Region from West Africa (Gambia) to northeast Africa (Sudan)
and south to South Africa (Cape Province), plus Rodriguez, Mauritius, and the
Seychelles. In the Neotropical Region, I have records from Brazil, Guyana, and El
Salvador, and from the West Indies (Bahamas, Puerto Rico, Virgin Islands,
Dominica, the Grenadines, and St. Vincent). In Oceanica, I know it from Hawaii,
Marquesas Islands, Samoa, Ellice Islands, and Fiji, and from Australia (Queensland,
New South Wales, Victoria, and South Australia).
4. Desmometopa lucidifrons, n. sp.
(Fig. 20)
Frons with short, weak, evanescent interfrontal plates, and anterior 2/5 of
frons shining.
Male, female. Black, gray to brownish gray microtomentose; knob of halter
lemon yellow; mid and hind tarsi yellow except for distal tarsomere or two.
Frons longer than broad (1.2x), with anterior 2/5 glistening, not a smooth and
polished appearance but with a peculiar sheen that helps to obscure the
interfrontal plales, the posterior 3/5 the usual subshining velvet black,
fronto-orbital plates and frontal triangle distinct but interfrontal plates obscure
and weak, evanescent, appearing to consist of 3 or 4 small, separate,
microtomentose areas surrounding bases of interfrontal setae, the posterior ends
of the plates about at level of foremost upper orbital bristles; frontal triangle
long and narrow, much longer than broad at base, apex about at level of posterior
ends of the plates; cheek narrow, barely over 1/3 breadth of 3rd antennal segment
and 1/9 the eye height, with distinct polished subocular crescent that is broadly
24 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
triangular anteriorly (fig. 20); face deeply concave in profile, the vibrissal angle
produced anteriorly nearly to a 45° angle, lateroventral corner of facial plate
shining and warped forward to exaggerate the angle; 3rd antennal segment small
in both sexes; palpus gently clavate in both sexes, that of male not enlarged;
proboscis slender in side view, but from above or below haustellum broadened
toward base, about 0.70x the distance between the vibrissae.
Thoracic pleuron gray microtomentose, including entire propleuron and areas
surrounding anterior spiracle; anterior slope of sternopleuron, poslerodorsad to
fore coxa, rather shining but entirely thinly microtomentose, without the
customary polished spot of most species of Desmometopa. Fore coxa and fore
femur not elongate. Length, 2 mm.
Holotype male, allotype, and 2 paratypes (male, female), TRINIDAD: Simla,
Arima Valley, Feb. 6-12, and 20-26 (allotype), 1966 (S.S. and W.D.
Duckworth)[Washington].
The peculiar sheen of the anterior part of the frons, which helps to obscure
the already short and weak, evanescent interfrontal plates, is a distinctive feature
of this species. Also, the species is apparently the only one of the subgenus
Platophrymyia in which the pleuron is entirely gray microtomentose, although
thinly so and hence somewhat shining on the anterior slope of the sternopleuron.
A Panamanian species, evanescens, has a frons suggestive of lucidifrons, but
evanescens has a large polished pleural spot.
The specific name is a noun in apposition derived from the Latin verb ieee,
to shine, combined with frons.
5. Desmometopa latigena, n. sp.
Cheek as in m-nigrum (fig. 28), broad and subequal to breadth of 3rd antennal
segment, with large subtriangular subocular crescent; pleuron anteriorly chiefly
polished.
Male, female. Chiefly black or brownish black; antenna and palpus black in
both sexes; knob of halter yellow; fore coxa brownish to black; proximal
tarsomere or two of mid and hind tarsi yellowish.
Frons with M-shaped frontal vitta dull, rather heavily bluish gray
microtomentose, the gray fronto-orbital and interfrontal plates and frontal
triangle only moderately distinct, a narrow velvet black spot along each side of
frontal triangle, which is long and reaches middle of frons; cheek subequal to
breadth of 3rd antennal segment and about 1/4 the eye height, with large
subocular crescent 1/2 or more as broad as cheek, approximately as figured for
m-nigrum (cf. fig. 7); vibrissal angle acute, nearly a 45° angle, and lateroventral
corners of facial plate shining black; 3rd antennal segment small in both sexes;
palpus gently clavate in both sexes.
Dorsum of thorax dark gray microtomentose; anterior 1/2 of pleuron chiefly
polished, including propleuron, most of mesopleuron, and anterior slope of
sternopleuron, the anterior spiracle almost surrounded by polished areas (fig. 28);
mesopleuron gray posteriorly. Fore coxa not elongate. Length, 1.7 mm.
Holotype male, allotype, and 13 paratypes (12 males, 1 female), TEXAS: Big
Bend National Park, Dagger Flats, 3500 ft., May 11, 1959 (W.R.M. Mason; “Ex
Yucca torrei"[Ottawa]; 3 female paratypes, CALIFORNIA: 2, Riverside Co.,
Cottonwood Spring, Apr. 12, 1950 (P.D. Hurd)[Berkeley], and 1, San Bernardino
Co., San Bernardino Mts., Hidden Valley, May 5, 1928 (A.L. Melander)
[Washington].
The broad cheek will readily distinguish this species from all other
Desmometopa except m-nigrum, sp. H, and postorbitalis, and from these by the
predominantly polished pleuron. The California females are far removed from the
Sabrosky: Desmometopa of the World 25
main series but seem to be conspecific. The fore coxa is definitely black,
compared with brownish yellow in the Texas specimens. However, most of the
latter appear to be slightly immature and not fully colored.
The specific name is a noun in apposition derived from the Latin latus, broad,
combined with gena, cheek.
6. Desmometopa sp. H
Two males from ALGERIA: Edough, August 1907 (P. Lesne; “des galeries du
Cossus de Moskat")[Paris], are Leneral, and the species is left unnamed until the
characters can be properly described. The cheek appears to be broad, which
would place it near m-nigrum, but the subocular crescent is narrow and bandlike,
unlike m-nigrum and similar species. The 3rd antennal segment is small. The
black palpus is almost capitate rather than clavate, broad and flat although not as
extreme as figured for gressitti (fig. 4). The black fore coxa is somewhat
elongate, and the fore femur distinctly elongate compared to the other femora.
As in m-nigrum and postorbitalis, the polished black spot posterodorsad to fore
coxa is large, including an anteroventral area of mesopleuron, and bilobed (cf. fig.
23).
7. Desmometopa microps |_amb
(Figs. 16,17)
racmmmrarescmmsens hu:
364 (Seychelles Is.)[London].
D. microps; Sabrosky, 1977, in Delfinado and Hardy (eds.), A Catalog of the
Diptera of the Oriental Region 3: 271.
. microps; Sabrosky, 1980, in Crosskey (ed.), Catalogue of the Diptera of the
Afrotropical Region, p. 686.
. tristicula part; Hennig, 1941, Ent. Beihefte aus Berlin-Dahlem 8: 177
[Pilam and Chipun, Formosa, specimens].
|O
lO
Near sordida but with broad postgenal and postorbital areas.
Male, female. Black, only the basal 1/3 of palpus orange-yellow in both sexes.
Frons with distinct interfrontal plates against velvet black frontal vitta;
frontal triangle large, equilateral, apex well in advance of median ocellus and
anterior to level of posterior ends of interfrontal plates; cheek relatively broad
(figs. 16,17), 7/10 the breadth of 3rd antennal segment and 1/4-1/3 the eye height,
with broadly rounded (female) to broadly triangular (male) polished black
subocular crescent; in male, postorbital area broad and convex up to vertex, with
a bulging appearance (fig. 17), as is the postgenal area, but in female the
postorbital area narrow but the subshining postgenal area, while relatively narrow
compared to that of male, is broader than in other females of the genus (fig. 16);
3rd antennal segment small in both sexes; face weakly concave, vibrissal angle not
produced anteriorly, only an 80°-90° angle; palpus moderately long, clavate in
both sexes.
Thorax predominantly bright gray microtomentose, brighter gray on sides,
including entire propleuron and area around anterior spiracle, with comparatively
small polished black spot, posterodorsad to fore coxa, that is not bilobed and does
not include an anteroventral area of mesopleuron (as in fig. 25). Fore coxa not
elongate. Length, 2-2.5 mm.
This is one of the most distinctive species of the genus in the male sex, but
the female is more easily confused except by the experienced eye. In the male,
26 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
the postorbital area, which extends broadly to the vertex (fig. 17), is convex and
together with the similar postgenal area can best be described as bulging.
Females of microps are easily confused with those of sordida, and older records of
“sordida" from the Oriental Region seem likely to be microps. The cheeks of the
two are similar in breadth and in the appearance of the polished subocular
crescent. The postorbital area, so broad in the male, is not obviously different in
females from that of sordida, but it is still clearly broader in microps. If the
specimen is teneral and the head collapsed, which is all too often in available
material, this feature can easily be misinterpreted. The difference in the color of
the palpi is a consistent difference, but if the palpi are withdrawn into the oral
cavity and the proboscis folded back, the color of the basal halves of the palpi is
not at all evident and those of microps might easily be misinterpreted as entirely
black.
Although microps is placed in the key near m-nigrum and_ other
broad-cheeked species, it is apparently not closely related. D. latigena has an
extensively polished pleuron, and m-nigrum, postorbitalis, and sp. H all have a
large, bilobed polished spot that includes an anteroventral area of the
mesopleuron (fig. 23). |
Distribution: Afrotropical Region (Seychelles, Tanzania, West Cameroun),
widespread in Oriental Region and bordering areas of Palearctic Region, from
Afghanistan and West Pakistan to Nepal, Manchuria and Japan, south to the
Ryukyu Islands (Okinawa), Taiwan, Java, Malaya, Thailand, and Sri Lanka; also
Guam.
8. Desmometopa postorbitalis, n. sp.
(Fig, 15)
Cheek broad, subequal to breadth of 3rd antennal segment, but postorbital
area broad below and rather broad dorsally up to vertical bristles, and continued
forward below eye as a broad subocular band (fig. 13).
Male, female. Chiefly black or brown-black; Ist and 2nd antennal segments
and part of 3rd reddish yellow; palpus yellow on basal 1/2 in female, chiefly
yellow in male; knob of halter yellow; fore coxa and all tarsi black.
Frons with upper orbital plates obviously broader than lower plates, the latter
and the interfrontal plates narrow and the sections of the M-shaped, subshining,
velvet black frontal vitta relatively broad; frontal triangle short, apex not quite
opposite upper ends of interfrontal plates; cheek broad, subequal to breadth of 3rd
antennal segment and over 1/4 the eye height; postorbital area in male broad up
to vertical bristles, widening below, postgenal area shining black and continued
forward beneath the eye as a broad band 1/2 or more as broad as cheek (fig. 13),
in female the postorbital and postgenal areas not as broad as in male; vibrissal
angle approximately a 90° angle, the lateroventral corner of facial plate flat and
dull gray; 3rd antennal segment small in both sexes; palpus gently clavate, not
large.
Thorax dark gray microtomentose; pleuron, posterodorsad to fore coxa, with
bilobed polished black spot, including adjoining broad anteroventral marginal area
of mesopleuron (as in fig. 23). Fore coxa somewhat elongate, but fore femur only
moderately so. Length, 2.25 mm.
Holotype male, allotype, and seven paratypes (3 males, 4 females), UGANDA:
Kigezi Province, Mabungo, 6000 ft., Nov. 1934 (J. Ford)[London, paratypes
Washington]. Other paratypes: male, female, UGANDA: Kigezi District, Mabungo
Camp, 6000 ft., Nov. 18, 1934 (J. Ford)[London, Washington]; male, female, Kigezi
District, Mt. Muhavura, Sept. 29, 1934 (F.W. Edwards)[London]; KENYA: male,
Molo, Mau Escarpment, 2420 m, Dec. 1911 (Alluaud and Jeannel) [Paris].
Sabrosky: Desmometopa of the World 27
This species is superficially similar to m-nigrum and has been confused with
it in the past because of the broad cheek. The key and figures will adequately
distinguish the two species, especially the males because of the broad upper part
of the postorbital area and broader postgenal area in postorbitalis. Females alone
will be more difficult: the postgenal area is narrower than in the male but there
is still the shining band continuing forward below the eye.
The specific name is an adjective referring to the postorbital area.
9. Desmometopa m-nigrum (Zetterstedt)
(Figs. 7,23)
Agromyza M nigrum Zetterstedt, 1848, Dipt. Scand. 7: 2743 (Sweden).
Desmametopa [sic] niloticum Becker, 1903, Mitt. Zool. Mus. Berlin 2: 188 (Nile
Valley, Egypt).
Desmometopa m-nigrum; Malloch, 1924, Proc. |_inn. Soc. N.S. Wales 49: 336
(Australia).
D. M. nigra; Duda, 1935, Natuurhist. Maandblad 24: 25.
D. m-nigrum of most European and American authors (e.g., Hennig, 1937;
Melander, 1913).
With unusually broad cheek and large triangular polished subocular crescent.
Male, female. Predominantly black, including all tarsi, only palpus in part
and knob of halter yellow; Ist and 2nd antennal segments and base of 3rd
sometimes dark reddish; body chiefly gray to brownish gray microtomentose.
Frons with M-shaped frontal vitta subshining velvet black and especially
large and distinct because of narrow gray interfrontal and fronto-orbital plates,
the latter narrower on lower orbital plate than on upper; frontal triangle usually
not extending quite to middle of frons and ending opposite or only slightly in
advance of posterior ends of interfrontal plates; cheek especially broad, appearing
equal to breadth of 3rd antennal segment or nearly so, and over 1/4 the height of
an eye, with large triangular polished subocular crescent (fig. 7); postgenal and
postorbital areas relatively narrow; vibrissal angle an 80° - 90° angle, the
latero-ventral corner of facial plate dull gray; face gently concave in profile; 3rd
antennal segment small in both sexes; palpus gently clavate, not large.
Thorax dark gray microtomentose, pleuron chiefly so but with large bilobed
polished black spot posterodorsad to fore coxa, the spot including an adjoining
broad anteroventral marginal area of the mesopleuron (fig. 23). Fore coxa and
fore femur not elongate in either sex. length 2-3 mm.
This well known species is distinctive because of lhe broad cheek with
triangular polished subocular crescent (fig. 7), as figured by Hennig (1937, fig.
34). Most specimens in collections are correctly identified, yet some confusion is
possible, as noted in the introduction. Johnson (1913) recorded m-nigrum from
Biscayne Bay and lake Worth, Florida (Mrs. Slosson), as determined by
Coquillett. I have not found these specimens, bul they may have been sordida,
judging from a Dallas, Tex. specimen of sordida [Washington] that was identified
by Coquillett as m-nigrum. Aldrich also at one time misidentified Hawaiian
material as m-nigrum, but the species is not known to occur there (see discussion
under “Identification” in the Introduction).
This species, along with postorbitalis and sp. H, not only has a
characteristically broad cheek but also a characteristically bilobed polished spot
on the pleuron (fig. 23). D. latigena, the fourth member of the group of
broad-cheeked species--microps is not really one of these, is quite different in
having the pleuron chiefly polished (fig. 28).
28 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
D. m-nigrum is virtually cosmopolitan, probably spread in commerce. It
occurs widely in the Palearctic Region, but most records are from southern
Europe, especially the Mediterranean Subregion. I have also seen material from
the Azores and Israel, and from northern Africa (Egypt, Algeria, Morocco). I have
seen numerous specimens from the Afrotropical Region, ranging from sub-Saharan
countries south to Cape Province, and from the Cape Verde Islands and St. Helena
to the Seychelles and Madagascar. In North America it is recorded from Iowa and
Michigan to New York and New Hampshire, south through the Atlantic and Gulf
Coast States to Texas, and from Arizona and California, as well as Bermuda.
Neotropical records are scattered but significant and suggestive of transport in
commerce: Mexico, Cuba, Dominica, Barbados, Ecuador, and Chile. In the
Oriental Region I have seen it only from India (Assam), Sri Lanka, and Pakistan. I
have seen it from Australia, from several localities in New South Wales, as
correctly recorded by Malloch (1924). I have not seen it from any of the Pacific
Islands, and published records from Fiji by Bezzi (1928) and from Hawaii by
Illingworth (1926) and others are misidentifications.
10. Desmometopa interfrontalis Sabrosky
(Figs. 9,10)
Desmometopa interfrontalis Sabrosky, 1965, Stuttg. Beitr. Naturk. 138: 3
(Tanzania) [Ludwigsburg].
With broad interfrontal and fronto-orbital plates, and correspondingly
reduced sections of the M-shaped frontal vitta.
Male, female. Chiefly black, palpus chiefly yellow, knob of halter yellow,
fore coxa yellowish to brown, and all tarsi chiefly yellow.
Frons with interfrontal and fronto-orbital plates broad and frontal triangle
long, 1/2 to 2/3 length of frons, so that the sections of M-shaped frontal vitta are
greatly narrowed, the inner arms of the M little over half as wide as an
interfrontal plate; cheek over 1/2 as broad as 3rd antennal segment and 1/6 the
height of an eye, entirely gray, without trace of subocular crescent; vibrissal
angle not produced, about a 90° angle; 3rd antennal segment small in both sexes;
palpus clavate.
Thorax heavily gray microtomentose, brownish gray on dorsum, brighter gray
on pleuron, with small polished black spot posterodorsad to fore coxa (cf. fig. 25),
the mesopleuron with anteroventral polished area; fore coxa not elongate.
Length, 1.5 mm.
Distribution: Cameroun, Ivory Coast, Liberia, Namibia, Nigeria, Tanzania,
Uganda, and Zaire. An exceptionally long series (151 specimens) was “bred from
decaying banana skins” at Mulago, Kampala, Uganda, Sept. 30, 1936 (E.G.
Gibbins)[{London].
The broad interfrontal stripes and parafrontals and the narrowed "M" of the
frontal vitta make this species unique in the genus.
11. Desmometopa evanescens, n. sp.
Frontal vitta shining velvet black, the interfrontal plates short, obsolescent.
Female (male unknown). Chiefly black, only the knob of halter and the mid
and hind tarsi, except for distal segment or two, yellow.
Frontal vitta shining velvet black from all angles of view, gray frontal
triangle and dark gray fronto-orbital plates distinctly delineated, triangle ending
at or near middle of frons and at or almost at level of the foremost upper orbital
bristles, the plates narrow throughout their length; interfrontal plates short and
Sabrosky: Desmometopa of the World 29
weak, poslerior ends well anterior to apex of frontal triangle, each plate linear
and usually interrupted, consisting of 2 to several small spots of microtomentum
surrounding bases of interfrontal setae; cheek narrow, slightly over 1/4 the
breadth of 3rd antennal segment and nearly 1/10 the height of an eye, with narrow
polished black subocular crescent that is linear posteriorly but widens anteriorly
(similar to fig. 18, but wider anteriorly); vibrissal angle produced to a 45° angle,
accentuated by shining black lateroventral corner of facial plate warped forward
even beyond the angle; face strongly concave in profile, parafacial not visible; 3rd
antennal segment not large; palpus gently clavate.
Thorax chiefly and heavily dark gray microtomentose; pleuron chiefly so but
with large polished black spot posterodorsad to fore coxa and including adjoining
area of mesopleuron (as in fig. 24), also with a median to posteromedian polished
spot on sternopleuron. Fore coxa not elongate, fore femur slender. Length, 1.5
mm.
Hololype and 8 paratypes, PANAMA: Panama Province, Las Cumbres,
various dates Jan. 31-Feb. 28, 1981 (holotype Feb. 28)(H. Wolda, at flowers of
Aristolochia)[Washington].
| The weak and evanescent interfrontal plates are suggestive of lucidifrons but
that species has entirely gray microtomentose pleuron. Some of the specimens
are slightly teneral, but even the darkest have the fore coxae slightly infuscated
proximally. I believe the species is best associated with the flavicoxa group,
because the fore coxae are at least partly yellowish. Should it be judged
otherwise at couplet 11, evanescens would run easily--at least disregarding the
"sharply distinct" interfrontal plates mentioned in couplet 25, 2nd part--to the
Old World species kandyensis and gressitti in couplet 46, both of which have long
and distinct interfrontal plates.
away.
12. Desmometopa sp. I
One female, BRAZIL: Sao Paulo, Nova Teutonia, July 7, 1937 (F. Plaumann)
[Helsinki] apparently represents a distinct species, but I forgo naming it until
material of both sexes is available. The apex of the long frontal triangle is
midway on the frons, approximately on a level with the posterior ends of the short
interfrontal plates and with the foremost upper orbital bristles. The cheek is
narrow, 1/3 the breadth of 3rd antennal segment and 1/9 the height of an eye,
with linear subocular crescent. The face is only moderately concave in profile
because the vibrissal angle is only slightly produced, although almost a 45° angle.
The pleuron is predominantly gray, including the entire propleuron and the areas
surrounding the anterior spiracle; the polished pleural spot is fairly large,
including an elongate-oval anteroventral area of the mesopleuron (as in fig. 24),
and there is a median polished spot on the sternopleuron. The halter knob is
brownish yellow, and I believe it is brown but immature rather than a discolored
yellow. The 3rd antennal segment is small and the fore coxa short, features usual
in females but not necessarily true of the males.
13. Desmometopa woldai, n. sp.
Fore coxa yellow, palpus black, and propleuron entirely gray microtomentose.
Female. Chiefly black, with strikingly contrasted yellow fore coxa; knob of
halter yellow; mid and hind tarsi yellow except distally.
30 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Frons with frontal vitta sudshining velvet black, the fronto-orbital plates,
narrow interfrontal plates, and frontal triangle gray and distinct; frontal triangle
moderately long, its apex usually at level of foremost upper orbital bristles; cheek
narrow, 1/3 breadth of 3rd antennal segment and 1/10 the height of an eye, with
linear polished subocular crescent that slightly widens anteriorly; face deeply
concave in profile, vibrissal angle strongly produced to a 45° angle, the
lateroventral corner of facial plate shining black and warped forward even beyond
the angle; 3rd antennal segment small; palpus clavate.
Thorax bright gray microtomentose; pleuron with large polished black spot
poslerodorsad to fore coxa, including anteroventral area on mesopleuron (as in fig.
24); sternopleuron with small to large polished spot mesally, just dorsal to apex of
mid coxa; propleuron entirely gray microtomentose, and anterior spiracle
completely surrounded by gray areas. Fore coxa not elongate, as usual in
females. Length, 1.75-2 mm.
Holotype female and 144 paratypes, all females, PANAMA: las Cumbres,
Panama Province, Nov. 1980-Feb. 1981 (H. Wolda, on flowers of Aristolochia
pilosa) [Washington].
The long series of topotypic females permitted a useful evaluation of
variation. The characters proved to be very consistent. The _ polished
sternopleural spot was always present, though varying in extent from a small
round spot (common) to a large subquadrate spot (uncommon, only a half dozen
specimens). One female, not a paratype, had exceptionally short and narrow
interfrontal plates, but it is probably only a variant. Some 32 other specimens are
more or less damaged and not included in the type series.
Most species of the flavicoxa group have the thoracic pleuron predominantly
polished, whereas flavicoxa and woldai have the sternopleuron chiefly gray
microtomentose with a mesal polished spot, usually small.
: A series of specimens, partly from widely scattered localities without good
series, partly specimens in poor condition, will key to woldai bul may represent
different species. I leave them unidentified for the present. All males have small
3rd antennal segment, ordinary clavate palpus, and slightly elongate fore coxa.
The various specimens differ from woldai as follows:
All tarsi yellowish: 3 females, Mexico, Costa Rica, and Colombia.
All tarsi black: 2 males, Panama (Canal Zone).
Sternopleuron entirely dull gray microtomentose: 2 males, Peru, Dominica.
Larger palpus in male: Trinidad, Tobago, Panama (Canal Zone).
Probably woldai: Mexico (Baja Calif., Michoacan), Honduras, Panama (Canal
Zone), Colombia, and possibly a male from southern Brazil (Nova Teutonia).
The specific name is in the genitive case. It is dedicated to the collector of
the magnificent series, ttenk Wolda, who has found many interesting species of
Desmometopa and Chloropidae visiting the flowers of Aristolochia in Panama.
Desmometopa flavicoxa Hendel, 1932, Konowia 11: 143 (n. Argentina)
[l_udwigsburg].
Species with narrow cheek, produced vibrissal angle, subshining velvet black
frontal vitta, yellow fore coxa, and entirely gray microtomentose propleuron;
male (presumed) with partly orange-yellow palpus.
Female (holotype). Chiefly black; antenna and palpus black; knob of halter
yellow; legs predominantly black, fore coxa yellow and contrasting strongly with
black pleuron; tibiae narrowly yellow basally; mid and hind tarsi chiefly yellow,
with distal tarsomere or two infuscated. Length, 2 mm.
Sabrosky: Desmometopa of the World 31
Frons with frontal vitta entirely subshining velvet black, with ocellar triangle
and fronto-orbital plates gray microtomentose; interfrontal plates distinct but
thickly microtomentose, ending posteriorly about midway of frontal vitta and just
short of apex of frontal triangle; cheek narrow, not 1/3 breadth of 3rd antennal
segment and 1/10 the height of an eye, gray-black with narrow polished subocular
crescent that is broader anteriorly; vibrissal angle produced as in tarsalis, the
angle about 45°, face decidedly concave in profile, and lateroventral corner of
facial plate shining black; 3rd antennal segment small in both sexes.
Thorax heavily dark gray microtomentose except for large polished black spot
posterodorsad to fore coxa, including a broad anteroventral area of the
mesopleuron (as in fig. 24), and a small polished black spot centrally on the
sternopleuron, the propleuron entirely gray and anterior spiracle completely
surrounded by gray areas. Fore coxa not elongate.
Through the kindness of Dr. B. Herting, I received for study a specimen that
is undoubtedly the holotype, although it was not so marked. The specimen is
labeled "Mis. Tacaagle/XI.25. Lindner/D.Chaco-Exped.” and “Desmometopa
flavicoxa H. [apparently in Hendel's handwriting]/F. Hendel det.", all agreeing
with the information published by Hendel, and in the appropriate collection. It
agrees with Hendel's description except that it is a female and not a male, which
was either a typographical error or an understandable mistake in these small black
flies with small genitalia. I have seen only one other specimen that can be
associated with it, a male that differs only in having the palpus partly yellow, a
not unexpected difference in males, and in even shorter and narrower interfrontal
plates.
Male, "Bemgerg” [sic!, probably Puerto Bemberg], Misiones, March 14-30,
1945 (Hayward, Willink, and Golbach)[Tucuman]. As described for female, but
interfrontal plates narrower and shorter, not reaching middle of frons and ending
well in advance of frontal triangle; palpus orange-yellow on more than basal half,
clavate, not broad and flat.
The combination of yellow fore coxa and entirely gray microtomentose
propleuron distinguishes this species from all but woldai. The latter has entirely
black palpus in the male.
15. Desmometopa sp. J
One male, PANAMA: Almirante, Bocas del Toro Province, Dec. 10, 1952
(F.S. Blanton)[Washington], is in poor condition and will not be named at this
time. It appears to represent a distinct species in the flavicoxa group. It is the
only one of that group with the frontal vitta dark gray microtomentose on the
anterior half. The palpi are missing, unfortunately. The yellow fore coxa is
elongate, and the prosternum and propleuron are concolorous with the fore coxa.
Other characters that can be noted are the pleuron almost entirely polished, knob
of halter yellow, and fore tarsus black. The other tarsi are discolored and may
have been reddish or yellowish. Like all others in the flavicoxa group, the
vibrissal angle is strongly produced and the face in profile is deeply concave. The
3rd antennal segment is small.
16. Desmometopa nigrohalteralis, n. sp.
Fore coxa yellow, pleuron almost entirely polished, and knob of halter black.
Male, female. Almost entirely black, only fore coxa and mid and hind tarsi,
except for distal segment or two, yellow; propleuron pitch black.
Frons with frontal vitta velvet black; frontal triangle large and chiefly
polished, with slight microtomentum on ocellar tubercle; interfrontal plates
32 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
exceptionally short and weak, little more than 1/3 length of frons and not strongly
marked; face deeply concave in profile and vibrissal angle produced to a 45°
angle; antennal grooves deeply concave and heavily gray microtomentose; cheek
narrow, 1/4 breadth of 3rd antennal segment and 1/10 the eye height, with
polished subocular crescent that is linear posteriorly but wider anteriorly; 3rd
antennal segment small in both sexes; palpus of male somewhat broad and flat but
not as extreme as figured for gressitti (cf. fig. 4).
Thoracic pleuron anterior to pleural suture all polished, as is the
pteropleuron. Fore coxa of male somewhat elongate but fore femur not so, both
slender. Length, 1.75-2 mm.
Holotype male and_ allotype, ARGENTINA: Villa Padre Monti,
Tucuman-Burruyacu, Jan. 17-Feb. 7, 1948 (R. Golbach)[ Tucum4n].
The black halter will distinguish this species from all others in the flavicoxa
group, and indeed from most other species of Desmometopa, in addition to the
uncharacteristic polished frontal triangle.
The specific name is an adjective referring to the black halteres.
17. Desmometopa sp. K
This species appears to be distinct, but I leave the lone male unnamed for the
present in the hope that additional material will be forthcoming. It is very close
to meridionalis in general habitus, with elongate yellow fore coxa, raptorial fore
leg, small 3rd antennal segment, and black and broad and flat palpus (cf. fig. 4)
but the mesopleuron has a broad gray band of microtomentum dorsally and
posteriorly, beginning at the anterior spiracle, and the fore femur is thinly gray
microtomentose, whereas meridionalis has polished black mesopleuron, and the
posterior surface of the fore femur is shining and chiefly polished.
BRAZIL: male, Rio de Janeiro, Nietheroy, July 20, 1915
(P.G. Russell)[ Washington].
18. Desmometopa glaucanota, n. sp.
(Fig. 27)
Fore coxa yellow; pleuron anterior to pleural suture chiefly polished, with
isolated postspiracular patch of gray microtomentum.
Male, female. Chiefly black, with palpus yellow on basal 1/2, knob of halter
yellow, fore coxa yellow, mid and hind tarsi yellow in female but infuscated
dorsally in male.
Frons with M-shaped frontal vitta subshining black and the long interfrontal
plates distinctly delineated; frontal triangle long acute, its apex well past the
posterior ends of the interfrontal plates; cheek very narrow, 1/4 breadth of 3rd
antennal segment and 1/12 height of an eye, with linear subocular crescent that is
slightly broader anteriorly; face deeply concave and vibrissal angle strongly
produced to a 45° angle, the lateroventral corner of facial plate highly shining
black and well warped forward and upward; antennal grooves deeply concave and
densely gray microtomentose; 3rd antennal segment small in both sexes; palpus
large, clavate.
Thoracic pleuron anterior to pleural suture almost entirely polished, with
postspiracular patch of gray microtomentum, and a narrow margin of same gray
on mesopleuron posteriorly and occasionally dorsally (fig. 27);-propleuron polished
on lower 1/2; pteropleuron gray microtomentose. Fore coxa and fore femur in
male slender and elongate, not incrassate and raptorial, in female ordinary.
Length, 1.75-2 mm.
‘Sabrosky: Desmometopa of the World 33
Holotype male, allotype, and 4 male paratypes, BELIZE: Corozal Town, Aug.
30, 1967 (G. and R. Lacy)[Washington]. Other paratypes [all Washington]:
MEXICO: male, Veracruz, Nov. 1963 (N.L.H. Krauss), and female, Territory
Quintana Roo, Canctin, July 16, 1974 (D.3. Pletsch). PANAMA: 95 females,
Panama Province, Las Cumbres, various dates 1980-82 (H. Wolda; on flowers of
Aristolochia).
In addition to the type series, about 60 other females from Las Cumbres,
Panama, not in suitable condition, were identified.
The pleuron is characteristic of this species, with the isolated spot of gray
microtomentum in the flat area just behind and a little above the anterior
spiracle. This is sometimes only a small patch, and that area often appears
shining, especially if the upper margin (notopleural ridge) is projecting and the
postspiracular area is thus depressed and concave. One will need to rotate the
specimen and view it at different angles to be sure. This spot is usually not
connected to any linear strip of microtomentum along the dorsal margin of the
mesopleuron.
The pattern of microtomentum on the pleuron is virtually the only difference
I find from floridensis. In the long series available, there is almost always a
polished break posterior to the postspiracular patch of microtomentum (fig. 27),
and rarely is there a continuous narrow band of microtomentum along the dorsal
margin of the mesopleuron. In floridensis, on the contrary, both dorsal and
posterior bands of microtomentum on the mesopleuron are broad (similar to fig.
26), and the microtomentum on the post-spiracular area does not appear as an
isolated patch.
The specific name is a noun in apposition derived from Latin glaucus, gray,
plus nota, referring to the spot of gray posterior to the anterior spiracle.
19. Desmometopa floridensis, n. sp.
Fore coxa yellow; vibrissal angle produced; frontal vitta velvet black; pleuron
extensively polished but broadly gray microtomentose behind anterior spiracle and
along dorsal and posterior borders of mesopleuron.
Male, female. Chiefly black; palpus yellow on approximately basal 1/2; knob
of halter and fore coxa yellow; tarsi brown-black in male, but in female mid and
hind tarsi yellow except distally.
Frons with M-shaped frontal vitta subshining velvet black; frontal triangle
not extending quite to middle of frons, ending approximately opposite posterior
ends of the narrow interfrontal plates; cheek narrow, slightly over 1/3 breadth of
3rd antennal segment and 1/9 height of an eye, subocular crescent strongly
broadened anteriorly; face deeply concave and vibrissal angle strongly produced to
a 45° angle; lateroventral corner of facial plate shining black and oral margin
strongly warped forward, especially at midline, shortening face and accentuating
the concavity of the antennal grooves; 3rd antennal segment small in both sexes;
palpus clavate.
Thorax dark gray microtomentose; pleuron anterior to pleural suture
extensively polished black, including part of propleuron, but mesopleuron broadly
gray along dorsal and posterior margins, including gray postspiracular area (as in
fig. 26). Fore coxa of male slightly elongate. Length, 2 mm.
Holotype male, allotype, and 4 paratypes (2 males, 2 females), FLORIDA:
Seminole Co., Sanford, Aug. 14, 1965 (G.W. Desin; Steiner trap)[Washington,
paratypes in Gainesville]. Other paratypes [Washington except as _ noted):
GEORGIA: male, Savannah, Feb. 3, 1954 (H.R. Dodge). FLORIDA: 7 females,
Clewiston, June 20, 1953 (M.R. Wheeler)[Austin], 2 females, Vero [Beach], Feb.
25, 1937 (J.R. Malloch); 3 females, Lake Worth, Jan. 16, 1929, “on asilid prey"
34 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
("S.W. Bromley Colln."); 3 females, Lee Co., Sanibel Island, May 11, 1973 (W.W.
Wirth, Malaise trap); male, Sweetwater, Apr. 15, 1969 (M.J. Kuck, “raqweed");
male, Merritt Island, Mar. 12, 1956 (H.V. Weems, Jr.)[Gainesville].
The pattern of gray microtomentum on the pleuron will distinguish this
species from the very similar species glaucanota (see discussion under that
species).
The specific name is an adjective derived from the name of the state of
Florida, the provenance of most of the specimens in the type series.
20. Desmometopa indistincta, n. sp.
Yellow fore coxa, unusually shining frons, and almost entirely polished
pleuron.
Male, female. Chiefly black; propleuron. (and sometimes humerus) and fore
coxa yellow; mid and hind tarsi yellow except for distal 2 or 3 tarsomeres; knob of
halter yellow; palpus sometimes obscurely yellowish toward base.
Frons shining black except for microtomentose ocellar tubercle and
parafrontals; interfrontal plates long, shining, without microtomentum and hence
only weakly distinguished from frontal vitta, the long frontal triangle likewise
shining and not microtomentose anterior to median ocellus; cheek narrow, less
than 1/2 breadth of 3rd antennal segment and 1/10 height of an eye, with polished
subocular crescent that is broader anteriorly; antennal grooves deeply concave,
densely gray microtomentose; face strongly concave in profile, vibrissal angle
produced to a 45° angle, and shining black lateroventral corner of facial plate
conspicuous and warped forward even beyond vibrissal angle; 3rd antennal
segment small in both sexes; palpus strongly clavate, broad and flat distally in
male (as in fig. 4), less broad in female.
Thoracic pleuron almost entirely polished, gray microtomentose only on
posterior slope and on upper part of pteropleuron, about the wing base. Fore coxa
moderately elongate in male but fore leg not raptorial, both ordinary in female.
Length, 2-2.25 mm.
Holotype male and male paratype, PERU: Iquitos, March-April 1931 (R.C.
Shannon); allotype, COLOMBIA: Rio Raposo, Feb. 1965 (V.H. Lee, light trap).
Paratypes: COSTA RICA: male, Turrialba, Nov. 1922 (Pablo Schild)[all
Washington]. ECUADOR: female, Pompeya, Napo R., Pastaza, May 14-22, 1965
(L. Pena)[Ottawa].
The shining frons with indistinct interfrontal plates and the almost entirely
polished pleuron will distinguish this species from others of the flavicoxa group.
The specific name is an adjective from the Latin indistinctus, indistinct or
obscure. :
21. Desmometopa meridionalis, n. sp.
With yellow fore coxa, and orange-yellow propleuron in male, sometimes in
female; pleuron anterior to pleural suture chiefly polished black.
Male, female. Predominantly black, strikingly marked in male with elongate
yellow fore coxa and orange-yellow propleuron; knob of halter yellow; mid and
hind tarsi yellow in both sexes except for distal 2 or 3 tarsomeres.
Frons with M-shaped frontal vitta subshining, velvet black, the dark gray
interfrontal and fronto-orbital plates and frontal triangle distinct against that
background; interfrontal plates extend back only to midlevel of frons and end
approximately opposite apex of long frontal triangle; cheek narrow, 1/3 breadth of
3rd antennal segment and 1/9 the height of an eye, with linear subocular crescent
that is wider anteriorly; face deeply concave as seen in profile, vibrissal angle
Sabrosky: Desmometopa of the World 35
produced to a 45° angle; polished black lateroventral corner of facial plate warped
forward, and with the strong facial carina leaves deeply concave, heavily gray
microtomentose antennal grooves; 3rd antennal segment small in both sexes;
palpus of male strongly clavate, broad and flat distally (cf. fig. 4), especially
striking in large specimens, palpus of female long but not broadly expanded.
Thoracic pleuron anterior to pleural suture almost completely polished,
except for narrow dorsal and posterior margins of mesopleuron and sparse
microtomentum on ventral portion of propleuron; postspiracular area polished;
pteropleuron gray microtomentose. Fore leg in male raptorial in appearance, fore
coxa elongate, 4 times as long as greatest width, with a row of rather strong
bristles, and fore femur clearly longer and larger than other femora, with an
anteroventral row of short, even, well-spaced bristles; in female, fore femur only
slightly elongate. Length, 1.5 - 3 mm (large males).
Holotype male, allotype, and 13 paratypes (11 males, 2 females), BRAZIL:
Nova Teutonia, 300-500 m, various dates (holotype, June 1964)(Fritz
Plaumann)[Ottawa]. Other paratypes: BRAZIL [all Washington]: 4 males, 3
females, Nova Teutonia, Sept. 1949 (2 females) and Apr. 1950 (F. Plaumann);
male, Rio Grande do Sul, Pelotas, Oct. 20, 1956 (C.M. Biezanko); male, Bahia,
Itabuna, Apr. 1973 (J.A. Winder); male, 3 females, Sao Paulo, Maua, May (N.L.H.
Krauss). URUGUAY: male, Montevideo, Jan. 25, 1965 (E.F. Legner)
[Washington]. PERU: 3 males, Iquitos, Mar.-Apr. 1931 (R.C. Shannon)
[Washington]. BOLIVIA: male, Chulumani, Yungas, Dec. 19-25, 1955, 1700 m
(L.E. Pena) [Ottawa]. ARGENTINA [Tucuman, except for last 7 specimens]: 8
males, 2 females, Villa Padre Monti, Tucuman-Burruyacu, Jan. 27-Feb. 7, 1948
(R. Golbach); 2 males, 1 female, Santiago del Estero, Montepotrere, Apr. 13, 1952
(A. Willink); female, Mendoza, Vista Flores, Jan. 31, 1950 (M.L. Aczél); 5 males,
Tucuman, Villa Padre Monti, Jan. 17-Feb. 7(3) and Mar. 7, 1948 (R. Golbach);
male, Tucuman: Alpechiri, Nov. 29, 1946 (R. Golbach); male, Tucuman, San
Javier, Nov. 18, 1946 (R. Golbach); male, Tucuméan, [locality illegible], Nov.
23-28, 1951 (Aczél & Golbach); 2 males, Salta, San Lorenzo, Jan. 20 (M.L. Aczél);
4 males, Salta, Urundel, Feb. 8-12, 1949 (M.L. Aczél)[Tucum4&n]; male, Salta,
Bella Vista, Embarcaci6n, Apr. 20, 1927 (R.C. Shannon); female, Misiones, Posa,
May (N.L.H. Krauss); female, Corrientes, 39 mi. s. Goya, Dec. 13, 1976; male,
Jujuy, Zapia, Apr. 10, 1927 (R.C. Shannon)[Washington]; 2 females, Salta, El
Carmen, 27 km _s. Molinos, 1900 m, Oct. 6, 1968 (L. Pena)[Ottawa]; female,
Catamarca, El Arenal, Oct. 3-4, 1968 (L. Pena)[Ottawa].
The males have the propleuron consistently orange-yellow in the fairly long
series available, and the palpus broad and flat as in gressitti (cf. fig. 4), and these
provide striking differences from blantoni in which the males have black
propleuron and ordinary clavate palpus. However, I have found no way to separate
females of the two species except by geography. The fore coxa and fore femur of
_ meridionalis are similar to those of saquaro (cf. fig. 22),
but narrower.
The specific name is a Latin adjective meaning southern, referring to the
geographic distribution of the specimens in the type series.
22. Desmometopa blantoni, n. sp.
Yellow fore coxa, predominantly polished pleuron, and black propleuron.
Male, female. Chiefly black, only fore coxa and knob of halter yellow, and in
the female mid and hind tarsi yellowish except for distal tarsomere or two.
Frons with M-shaped frontal vitta subshining, velvet black, the interfrontal
and fronto-orbital plates brownish gray and distinct but narrower than usual, the
36 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
interfrontal plates short, posterior ends about at midlevel of frons and about
opposite apex of frontal triangle; triangle mostly shining anterior to median
ocellus, the microtomentum usually confined to ocellar tubercle; cheek narrow,
1/4 breadth of 3rd antennal segment and 1/15 height of an eye, with linear
subocular crescent that is slightly wider anteriorly; face deeply concave in
profile, vibrissal angle produced to a 45° angle (cf. fig. 18), the lateroventral
corner of facial plate shining black and warped forward; antennal grooves deeply
concave, densely gray microtomentose; 3rd antennal segment small in both sexes;
palpus gently clavate in both sexes, only slightly larger in male.
Thoracic pleuron entirely polished anterior to pleural suture, except for
sublinear gray margin posteriorly on mesopleuron and sternopleuron; pteropleuron
entirely gray microtomentose. Fore coxa moderately elongate in male, nearly 4
times as long as greatest breadth, with short but strong bristles ventrally.
Length, 1.5 mm.
Holotype male, allotype, and a feriele paratype, PANAMA: Canal Zone,
Camaron, Ft. Kobbe, June 23, 1952 (F.S. Blanton, light trap) [Washington].
Paratypes [Washington except as noted]: PANAMA : female, Canal Zone, Colén,
July 2-14, 1979 (E. Broadhead et al., canopy fogging of Hura crepitans L. in humid
forest). COSTA RICA: male, Cartago, Nov. 1965 (N.L.H. Krauss); 2 females,
[Farm] La Caja, 8 km w. of San José, 1930 (H. Schmidt)[Eberswalde]. |
EL SALVADOR: male, San Andrés, Apr. 7, 1952 (P.A. Berry). MEXICO: 3 males,
1 female, Nayarit, 15 km n. of Chapalilla, July 19, 1951 (P.D. Hurd)[Berkeley];
male, Jalisco, Barra de Navidad, Sept. 1965 (N.L.H. Krauss); female, Veracruz,
Fortin de Las Flores, June 1964 (F.S. Blanton, light trap).
This species is closest to meridionalis. The males appear to be distinct on the
basis of the color of the propleuron and the form of the palpus (see under
meridionalis), but I have been unable to separate females of the two species.
The specific name is in the genitive case, and is dedicated to my good friend,
F.S. Blanton, who carefully saved much interesting material from his years in the
Panama Canal Zone.
23. Desmometopa terminalis, n. sp.
Almost entirely black, with knob of halter yellow and 5th tergum and male
terminalia orange-yellow.
Male. Black, dark gray microtomentose, only knob of halter yellow and apex
of abdomen orange-yellow, including posterior edge of 4th tergum, all of 5th, and
all terminalia.
Frons broader than usual in male, approximately square; frontal vitta dull
black, not velvet black, but the gray interfrontal and fronto-orbital plates and
frontal triangle are distinct; interfrontal plates relatively long, divergent, widely
separated, the interval between them much wider than between one of them and a
fronto-orbital plate; frontal triangle relatively short, its apex only slightly in
advance of median ocellus; cheek about 1/2 breadth of 3rd antennal segment and
1/5-1/6 height of an eye, with subtriangular subocular crescent that is at its
widest 2/5 as broad as cheek; face weakly concave in profile, vibrissal angle not
produced and approximately a 90° angle, the lateroventral corners of facial plate
dull gray and not developed; 3rd antennal segment relatively large, nearly
reaching lower margin of face, but not strikingly enlarged as in magnicornis;
palpus small, clavate.
Thoracic pleuron densely bright gray microtomentose, including all
propleuron and areas surrounding anterior spiracle, with large polished black area
posterodorsad to fore coxa that includes an anteroventral area of mesopleuron but
is not bilobed (cf. fig. 24). Fore coxa ordinary, convex and not elongate, only 2/3
length of fore femur. Length, 1.25 mm.
Sabrosky: Desmometopa of the World 37
Holotype male, PALAU ISLANDS: Koror Island, Mar. 15, 1953 (J.W.
Beardsley)[Honolulu].
The yellowish terminalia are unique in the genus as far as known, and thus I
have presumed to describe this single specimen. As in other Old World species,
the vibrissal angle is not produced. Possibly it is near ciliata. The subgenal
bristles are present on one side only, and the 2nd from the vibrissa is upturned and
longer than the others, although still much shorter and weaker than a vibrissa.
The setae on the section of costa between the costal breaks are few in number,
which would also tend to associate the species with cilata, although there are
other species which also show a small number of such setae.
The specific name is an adjective referring to the terminalia and the apex of
the abdomen, from the Latin referring to boundaries.
24. Desmometopa obscurifrons, n. sp.
Frons uniformly dull, heavily brownish gray microtomentose, interfrontal and
fronto-orbital plates and ocellar triangle not strongly contrasting with frontal
-vitta; pleuron with large polished black spot posterodorsad to fore coxa.
Male, female. Chiefly black, but with considerable yellow to orange-yellow
color on lunule, all antennal segments except narrowly dorsally, palpi chiefly, and
proboscis; all tarsi yellow except distal tarsomere or two; knob of halter whitish
yellow.
Frons uniformly dull brownish gray from most angles of view, often
changeable to greenish brown from certain angles, the interfrontal and
fronto-orbital plates and the frontal triangle scarcely evident, not strongly
contrasting with frontal vitta and thus not delineating the usual black "M" of most
species of Desmometopa; cheek narrow, 1/4 breadth of 3rd antennal segment and
1/12 height of an eye, with linear polished subocular crescent; face concave in
profile, the vibrissal angle produced to a 45° angle, and lateroventral corner of
facial plate, mesad of the vibrissal angle, at least partly shining black; 3rd
antennal segment small in both sexes; palpus clavate; proboscis especially
elongate and narrow.
Thorax heavily brownish gray microtomentose; pleuron with large polished
black spot posterodorsad to fore coxa, including broad anteroventral area on
mesopleuron (cf. fig. 24), this coxa not elongate in male. Length, 2.25 mm.
Holotype male, PANAMA: David, Chiriqui, 2200 ft., July 24, 1964 (A. Broce,
light trap); allotype, Panama Province, Las Cumbres (H. Wolda, on flowers of
Aristolochia pilosa)[Washington]. Paratypes [Washington except as _ noted]:
PANAMA: 8 females, Panama Province, Las Cumbres (Henk Wolda, on flowers of
Aristolochia pilosa); 4 males, 5 females, Almirante, Arraijan, and in the Canal
Zone, Mojinga Swamp at Ft. Sherman, and Summit Gardens (all, F.S. Blanton).
MEXICO: male, female, Vera Cruz, Fortin de Las Flores, June 1964 (F.S. Blanton,
light trap). EL SALVADOR: female, Santa Tecla, June 3, 1958 (O.L. Cartwright).
COSTA RICA: male, San José, July (H. Schmidt); 2 females, [Farm] La Caja, 8
km w. of San José, 1930 (H. Schmidt)[Eberswalde]. COLOMBIA: 4 males, Rio
Raposo, May 1964 and Feb. 1965 (V.H. Lee, light trap), ECUADOR: male, 22
females, Pichilingue, 1976 and April 1978 (E.J. Mendoza); female, Rircay Azuay,
Oct. 31, 1954 (R. Levi-Castillo); female, Sta. Domingo, Pichincha, June 19, 1965,
600 m (L. Pena) [Ottawa]. TOBAGO: male, two females, St. John Prov.,
Charlotteville, Mar. 14-21, 1979 (D. Hardy and W. Rowe).
This characteristic species is distinct from all other Desmometopa except
nigeriae by the uniformly dull frons. The interfrontal plates, parafrontals, and
frontal triangle are present but indistinct, and one does not see the usual black
M-shaped frontal vitta of almost all species of Desmometopa.
38 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
A small series from PERU: Huanuco, Tingo Maria, Apr. 19-24, 1969 (P. & P.
Spangler) and Iquitos, Mar-Apr. 1931 (R.C. Shannon), and another from
TRINIDAD: Simla, Arima Valley, Feb. 6-12 and 13-19, 1966 (S.S. and W.D.
Duckworth, black light) [both Washington] are referred here tentatively. The
pleuron appears to vary from a large polished spot posterodorsad to fore coxa,
through limited polished areas, in some cases only a narrow anteroventral area of
mesopleuron, to entirely gray pleuron, but the immaturity of some specimens
introduces an element of uncertainty.
The specific name, a noun in apposition, is derived from Latin obscurus,
indistinct, plus frons.
25. Desmometopa parafacialis, n. sp.
Frons heavily gray microtomentose, antenna and palpus black, and parafacial
visible in profile.
Male, female. Black, densely gray to bright gray microtomentose, only knob
of halter yellow; tarsi sometimes yellowish basally, especially in females.
Frons densely gray to brownish gray microtomentose viewed from any angle,
fronto-orbital plates distinct but interfrontal plates indistinct or not visible from
in front, slightly shining and therefore visible from behind, the plates rather
narrow and short, posterior ends at level of foremost upper orbital bristles, which
are also about the level of apex of frontal triangle; cheek bright gray, of
moderate width, barely over 1/2 breadth of 3rd antennal segment and 1/5 height
of an eye, with narrow polished subocular crescent that widens anteriorly and
continues as a polished area halfway up a parafacial, which is visible in profile;
face deeply concave, vibrissal angle strongly produced anteriorly, at about a 45°
angle, even beyond level of anterior margin of frons; lateroventral corner of
facial plate shining black and warped forward even beyond vibrissal angle; 3rd
antennal segment small in both sexes; palpus gently clavate in female but very
broad and flat in male (cf. fig. 4).
Thoracic pleuron densely gray microtomentose, including entire propleuron
and areas surrounding anterior spiracle, with polished black spot posterodorsad to
fore coxa that includes anteroventral area of mesopleuron (cf. fig. 24). Fore coxa
and fore femur in male somewhat elongate, former nearly 3 times as long as
broad. Length, 1.5-2 mm.
Holotype male, allotype and 39 paratypes (27 males, 12 females), TEXAS:
Austin, Nov. 9 and 13, 1958 (Lynn Throckmorton)[holotype, allotype, and
paratypes in Washington, paratypes in Austin]. Other paratypes, TEXAS: 2 males,
10 mi. s. Charlotte, Sept. 15, 1955 (W.L. Downes)[Lansing], 2 females, Llano
River, Kimble Co., May 23, 1972 (W.W. Wirth, Malaise trap)[Washington]; 2 males,
Big Bend National Park, Oak Spring, 4500 ft., May 1, 1959, and Panther Junction,
3500 ft., May 14, 1959 (both, J.F. McAlpine)[Ottawal. MEXICO: 3 males, 10 mi.
ne. San Luis Potosi, 6200 ft., Aug. 22, 1954 (R.R. Dreisbach) [Lansing], and 2
males, same data (J.G. Chillcott)fOttawal; 3 males, Hidalgo, Pachuca, 1700 ft.,
July 29, 1954 (3.G. Chillcott)[Ottawa]; male, female, Nayarit, Ahuacatlén, July
18-22, 1951 (P.D. Hurd, on flowers of Donnellsmithia Hintonii) [Berkeley]; male,
Durango, Nombre de Dios, Aug. 5, 1951 (P.D. Hurd, [flowers of?] Keysenharatia
polystachya) [Berkeley]; male, Puebla, Tehuacan, June 23, 1951 (P.D. Hurd)
[Berkeley].
The parafacial visible in profile will separate this species from most of those
in the genus, and certainly from those in the subgenus Platophrymyia with dull and
densely microtomentose frons.
The specific name is an adjective referring to the parafacials.
Sabrosky: Desmometopa of the World 57
26. Desmometopa atypica, n. sp.
(Fig. 12)
Frons heavily gray microtomentose, antenna and palpus black, and parafacial
not visible in profile.
Female. Black, heavily gray microtomentose; knob of halter, and mid and
hind tarsi except for distal segment or two, yellow; palpus obscurely yellowish
dorsally toward base.
Frons as described for parafacialis, the short and narrow interfrontal plates
sometimes visible as slightly shining lines, from other angles not evident; cheek
narrow, 1/2 breadth of 3rd antennal segment and 1/7-1/8 eye height, with polished
subocular crescent almost 1/2 breadth of cheek (fig. 12); parafacial midway not
visible in profile; face moderately concave in profile, vibrissal angle somewhat
produced anteriorly but not as much as in typical members of the subgenus, about
a 70° angle; lateroventral corner of facial plate shining black and slightly warped
forward; 3rd antennal segment small, palpus gently clavate.
Thoracic pleuron densely gray microtomentose, including entire propleuron
-and areas surrounding anterior spiracle, with rather large polished spot postero-
dorsad to fore coxa, including anteroventral area of mesopleuron (cf. fig. 24).
Fore coxa not elongate, and with no suggestion that it might be elongate in males,
but this is not certain. Length, 1.5 mm.
Holotype female and 12 paratypes, all females, PANAMA: Panama Province,
Las Cumbres, Nov. 19 (holotype), 21, and 22, 1980, Jan. 24, Feb. 22, Nov. 16, and
Dec. 1, 1981, and 4 undated (H. Wolda)[Washington]; female, ECUADOR: Sto.
Domingo, Pichincha, June 19, 1965, 600 m (L. Pena)[Ottawa]; female, PERU:
Iquitos, March-April 1931 (R.C. Shannon)[Washington].
This species is obviously very close to parafacialis, but the narrow parafacial
and the less distinctly produced vibrissal angle will distinguish it. In side view the
heads are quite different, that of parafacialis with head somewhat elongate and
long axis of eye diagonal, that of atypica with head not elongate and long axis of
eye vertical. :
I have isolated females from far distant places that may indicate a wider
Neotropical distribution, but unrecognized species may be involved, and they are
not included in the type series: BRAZIL: Sao Paulo, Nova Teutonia, Nov. 1958 (F.
Plaumann)[Ottawa]; TRINIDAD: Simla, Arima Valley, Feb. 20-26, 1966 (S.S. and
W.D. Duckworth)[Washington].
The specific name is an adjective referring to the atypical appearance of the
head compared with typical members of the subgenus Platophrymyia.
2/7. Desmometopa ciliata Hendel
(Figs. 11, 24)
Desmometopa ciliata Hendel, 1919, Ent. Mitt. 8: 200 (Sydney, New South Wales)
[Budapest].
Dark gray, resembling a small sordida but with knob of halter yellow; strong
subgenal bristle. ,
Male, female. Chiefly black or black-brown; knob of halter yellow.
Frons slightly broader than long, with velvet black M-shaped frontal vitta
delineated by strong gray interfrontal and fronto-orbital plates and frontal
triangle, the interfrontal plates moderately long and strong, extending posteriorly
to level of hindmost upper orbital bristles, the fronto-orbital plates broader than
40 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
usual; frontal triangle short and approximately equilateral, apex not midway of
frons; cheek 2/3 breadth of 3rd antennal segment and 1/5-1/4 height of an eye,
with relatively broad polished subocular crescent, and 2nd subgenal seta behind
the vibrissa developed as a strong, upcurved bristle (fig. 11); face only weakly
concave in profile, and vibrissal angle not produced, a broadly rounded 80°-90°
angle; 3rd antennal segment small in both sexes, little larger than 2nd segment;
palpus clavate.
Thorax dark leaden gray microtomentose; pleuron chiefly gray, including
entire propleuron and areas surrounding anterior spiracle, with large polished
black spot posterodorsad to fore coxa that includes an anteroventral area of
mesopleuron, the anterior margin of spot more or less straight (fig. 24), not
bilobed as in m-nigrum (cf. fig. 23). Fore coxa of male not elongate. Section of
costa between humeral crossvein and subcostal break with 8-10 coarse and
well-spaced setae. Length, 2 mm.
Hendel's original series consisted of five specimens. Through the kindness of
Dr. F. Mihdlyi of the Hungarian National Museum at Budapest, I was loaned a
male and 3 females of the original series, each specimen labeled "Typus”. The
male, which is in good condition and bears Hendel's identification label, is hereby
designated lectotype and has been so labeled. I have also seen the fifth syntype,
now a paralectotype, in the Museum in Vienna.
I have seen barely a dozen additional specimens of the species, from several
localities in New South Wales, and from South Australia and the Australian
Capital Territory. It may be an endemic Australian species.
Hendel's brief characterization gave few details and emphasized the bristling
of costa between the costal breaks, 8-10 well-spaced bristles in ciliata but 14-16
in other species. The type series reveals that an even better character is the
development of a strong subgenal bristle, often subequal to a vibrissa. The
association of this character and the smaller number of coarse setae on the costa
before the subcostal break is found in ciliata and a few Oriental species and may
be said to link these as a “ciliata group”.
Malloch's D. ciliata was a misidentification of D. inaurata Lamb, both in 1924
(p. 336) from New South Wales and in 1936 (p. 327) from Samoa, as revealed by
Malloch-labeled specimens in Washington.
28. Desmometopa leptometopoides, n. sp.
(Fig. 19)
Of the sordida group but with yellow halter knob, small polished spot on
pleuron, and Leptometopa-like broad and flat hind tibia.
Male, female. Chiefly black, densely gray microtomentose; palpus
orange-yellow, infuscated distally and below, more so in female than in male;
knob of halter yellow.
Frons with interfrontal and fronto-orbital plates and frontal triangle
distinctly well developed, the sections of M-shaped frontal vitta narrower than
usual; frontal triangle long, its apex at middle of frons, posterior portions of
interfrontal plates separated from triangle by approximately the width of one
plate; cheek of moderate width, 1/2 breadth of 3rd antennal segment and 1/8
height of an eye, with narrow but distinct polished subocular crescent; face
weakly concave in profile, vibrissal angle 80° to 90°, not produced anteriorly in
profile; 3rd antennal segment small in both sexes, only a little larger than 2nd
segment; palpus clavate.
Thoracic pleuron densely gray microtomentose, including all propleuron and
areas surrounding anterior spiracle; polished spot on pleuron posterodorsad to fore
coxa rather small and confined to anterior slope of sternopleuron, no polished area
Sabrosky: Desmometopa of the World 4]
anteroventrally on mesopleuron (cf. fig. 25). Fore coxa not elongate; hind tibia of
male broad and flat (fig. 19) as in males of Leptometopa. Length, 1.5 - 2 mm.
Holotype male, allotype, and one female paratype, LIBERIA: Suakoko, July 1,
1952 (C.C. Blickenstaff)[Washington]. Paratypes: GHANA: 5 females, Accra,
Aug. 16, 1945 (M.A. Locke)[Washington]; female, Accra, Dec. 1921 (J.W. Scott
Macfie, “reared from mud and debris collected from pools” [London]; female,
Legon, Apr. 6, 1969 (O.W. Richards, at light)[London]. CAMEROUN: 8 females,
Victoria, Dec. 22, 1920 (L.H. Booth)[London]. N. NIGERIA: male, 3 females,
Zaria, May 23, 1966 (J.M. Lyall, "Tenebrio/Trib culture window") [London].
TUNISIA: male, Bou Hedma, Apr. 11, 1976 (M. Olsson) [Lund].
One female, not a paratype, is not in good condition but appears to be this
species. If correct, it would represent a considerable extension of the known
range: CAPE PROVINCE, Mossel Bay, Dec. 15, 1928 (R.E. Turner)[lLondon].
The striking feature of broad and flat hind tibia in the male, resembling that
of Leptometopa, is unique in Desmometopa. Females are much less distinct,
however. The occasional lengthening of the subgenal setae might suggest ciliata,
but the small polished pleural spot of leptometopoides separates it from ciliata
and associates it with varipalpis and singaporensis. The elongated palpi of these
two species easily distinguish the males from leptometopoides, but females are
less distinctive. Females of varipalpis have a definitely broader cheek, but
females of singaporensis are much closer. Teneral females of leptometopoides
have yellowish cheeks and could on that basis alone have been confused with
singaporensis. Associated males give the best basis for identification.
The specific name is an adjective derived from the generic name
Leptometopa plus oides, like.
29. Desmometopa varipalpis Malloch
(Figs. 1,3,6,25)
Desmometopa varipalpis Malloch, 1927, Proc. Linn. Soc. N.S. Wales 52: 7 (New
South Wales) [Sydney]. |
. tarsalis Loew; Hennig, 1937, Fam. 60a. Milichiidae et Carnidae, p. 44, in
Lindner (ed.), Fliegen Palaeark. Region, Lfg. 115.
. singaporensis (tarsalis of European records); Hennig, 1939, Arb. Morph.
Taxon. Ent. Berlin-Dahlem 6: 87-88.
. M-nigrum (Zetterstedt); Wolcott, 1951, Jour. Agr. Univ. Puerto Rico 32(3):
529 (Puerto Rico, at least in part: the San Juan specimen, now in Washington,
is varipalpis).
OO So
|O
D. varipalpis; Lee, Crust, and Sabrosky, 1956, Proc. Linn. Soc. N.S. Wales 80:
339 (footnote on presumed holotype).
D. singaporensis; Hennig, 1965, Stuttg.Beitr. Naturk. 139: 2, fig. 1 (Iran;
figs. of male and female palpi).
D. singaporensis; Sabrosky, 1973, Family 75, p. 2, in A Catalogue of the
Diptera of the Americas South of the United States.
D. varipalpis (singaporensis, authors, in part); Sabrosky, [1977], p. 271, in
Delfinado and Hardy (eds.), A Catalog of the Diptera of the Oriental Region,
p. 271. 3
D. singaporensis; Hardy and Delfinado, 1980 (June 4), Insects of Hawaii 13:
355-6 (Hawaii; figs. of head and male genitalia).
. Varipalpis (singaporensis, authors, in part); Sabrosky, 1980 (July 10,
Family Milichiidae, p. 687, in Crosskey (ed.), Catalogue of the Diptera of the
Afrotropical Region.
\
42 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Polished pleural spot small, not including an area of mesopleuron;
fronto-orbital plates relatively broad (fig. 25); palpus of male strikingly elongate,
fusiform (fig. 3).
Male, female. Black, heavily gray microtomentose; cheek yellowish in ground
color; Ist and 2nd antennal segments almost always reddish, contrasting with
black 3rd segment; palpus partly yellow, extensively so in the enlarged palpus of
male, yellow on proximal 1/2 in female; knob of halter yellow; mid and hind tarsi
yellowish except distal 2, rarely 3, tarsomeres.
Frons (fig. 1) with velvet black frontal vitta, the interfrontal and
fronto-orbital plates and frontal triangle gray and distinct; frontal triangle
equilateral or slightly longer, reaching about to middle of frons; fronto-orbital
plates especially broad, each almost twice width of an interfrontal plate, and
without or almost without break between upper and lower orbital plates, unlike
singaporensis (cf. figs. 1,2); cheek (fig. 3) over 1/2 breadth of 3rd antennal
segment and about 1/5 height of an eye, with narrow polished subocular crescent;
parafacial narrowly visible throughout in profile; face weakly concave in profile,
vibrissal angle about 80° - 90°, not strongly produced, the lateroventral corner of
facial plate dull and not warped forward; 3rd antennal segment small in both
sexes; palpus gently clavate in female, but elongate fusiform in male (fig. 3),
narrowed apically, usually large and long, occasionally in small specimens short
and not so narrowed apically.
Thoracic pleuron heavily and extensively gray microtomentose, with small
polished spot posterodorsad to fore coxa, mesopleuron not _ polished
anteroventrally (fig. 25). Fore coxa and femur not elongate. Section of costa
between the humeral and subcostal breaks with many (12-14) short, semierect
setae, each only a little longer than diameter of costa. Length, 2.5 mm.
A specimen found in Malloch's collection years ago, still before me but to be
returned to Australia, is undoubtedly the holotype of varipalpis. It agrees
perfectly with the specimen data and the description but is labeled "Desmometopa
varicornis Type.” No doubt Malloch changed this in publication upon realizing
that he really meant the name to refer to the palpus and not the antenna. It is a
male, not a female as stated by Malloch. He clearly described the palpi as “large”
and "lanceolate," an attribute not then recognized as characteristic of males only.
Males of this species are very distinctive because of the elongate fusiform
palpi, unique in the genus and comparable only with singaporensis which also has a
large palpus but a capitate one (cf. figs. 3,5). However, females are much less
distinctive and may easily be confused with those of singaporensis and perhaps
with leptometopoides, and even with some other species (e.g., m-nigrum) if the
specimens of the last named are teneral with collapsed cheeks. Two
characteristics distinguish varipalpis from singaporensis in both sexes, and these
are useful for females: (1) in varipalpis (fig. 1) the fronto-orbital plates are broad
throughout, without an obvious break between the upper and lower orbital plates,
whereas in singaporensis (fig. 2) the fronto-orbital plates are narrower, especially
the lower orbital plate, and there is a distinct break and narrowing from upper to
lower sections; (2) the cheek is wider in varipalpis than in singaporensis (cf. figs.
3,5), a consistent difference but one that can be tricky because in teneral
individuals the cheek tends to fold longitudinally toward the eye, thus narrowing
the cheek.
The antennae are usually entirely black in singaporensis, but with reddish lst
and 2nd segments in varipalpis. However, enough specimens of singaporensis also
have these segments more or less reddish that the character cannot be relied
upon, although the bright segments in typical varipalpis will be a supporting
character.
Sabrosky: Desmometopa of the World : 43
Males of varipalpis have the additional characteristic of elongate fusiform
palpi, but in a few cases, almost always small individuals, the palpi are relatively
short and small and in such cases they appear less acute apically. In some long
series that are available from the same place and time, there are usually a few
small specimens with small palpi, which encourages me to believe that the
condition of small palpi represents only an occasional variant. In small specimens
of singaporensis, small palpi also occur, and such individuals are difficult to
identify with assurance except for the reliable character of the narrower
parafrontals. In males, the larger the specimen, the more elongate and
conspicuous appear the palpi, whereas in small specimens the palpi are shorter and
sapically they are less acutely angled.
There has been almost no confusion in the use of the name varipalpis, except
for Hennig's synonymizing of it with palpalis, undoubtedly misled by Malloch's
incorrect statement of the sex of the holotype. The real confusion has been in the
use of the name singaporensis, to which I myself, regretfully, have contributed.
See the discussion under that species for the effect of the lectotype designation
by which singaporensis must be applied to palpalis for the species with elongate
and capitate palpi in the males, leaving varipalpis the valid name for the species
with elongate and fusiform palpi. Hardy and Delfinado (1980) figured the quite
different palpi of the two species, with singaporensis under the synonymous name
tristicula (their fig. 143c) and varipalpis under the name singaporensis (their fig.
143a). For further discussion of the confused usage, see the introductory section
on "Identification". If it will alleviate the pain of name changing, I can note that
even if singaporensis had been restricted to the species here called varipalpis, the
frequently used name palpalis would have had to be changed to the rarely used
tristicula, which has priority.
Distribution: Widespread, occurring in all faunal regions, summarized as
follows to show the wide range (records from planes and ships not included):
Nearctic: Canada: Quebec (Montreal); U.S.A.: records from 23. states,
Wash.-Mich.-N.Y., south to Calif.-Texas-—Fla.
Neotropical: Bolivia, Brazil (Santos, Sao Paulo), El Salvador, Guatemala,
Mexico (Veracruz), Panama, and islands Antigua, Clipperton Island, Cuba,
Galapagos, Puerto Rico, St. Vincent, Virgin Islands.
Palearctic: Algeria, Egypt, Iran, Iraq, Israel, Saudi Arabia. [The record from
Hyéres, southern France, published by Séguy (1934) as D. albipennis (Meigen) with
singaporensis in synonymy, and mentioned by Hennig (1937) as tarsalis, was
actually based on D. m-nigrum, from the female specimen in Paris].
Afrotropical: Djibouti [as French Somaliland], Ghana, Kenya, South Yemen
(Aden), Sudan, Uganda, Yemen, Zaire, also Ascension Island.
Oriental: India (West Bengal, Tamil Nadu), Singapore, Thailand.
Australian: New South Wales.
Oceanica: New Guinea, Bismarcks, Bonins (Chichi Jima), Carolines (Lukunor
Atoll, Truk), Guam, WHawaii, Johnston Island, Marianas (Saipan), Marshalls
(Eniwetok Atoll, Jaluit Atoll, Kwajalein, Ujelang Atoll), New Hebrides (Espiritu
Santo), Volcanos (Iwo Jima), Wake Island.
A number of records suggest the probable importance of commerce in the
distribution of varipalpis: Guam, from planes (China Clipper and Honolulu
Clipper); Honolulu, Hawaii, plane from New Zealand and New Caledonia;
Liverpool, England, “from ship in Liverpool docks ex Canada"; Port Adelaide,
South Australia, “taken on ship ex Kuwait"; Valparaiso, Chile, "on board Santa
Inez" [undoubtedly the specimen called m-nigrum by Malloch, 1934b]; New
Orleans, La. from Central America; New York, N.Y., "larvae in potatoes in ship
from Argentina”, and "plane from Buenos Aires"; Norfolk, Va., "specimens in soil
with potatoes from Colombia".
44 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Perhaps it is only chance, but I have seen only one specimen of singaporensis
bearing any similar information, although the rearing records noted under
"Biology" would indicate the similar possibility of transport in commerce or
movement of people.
Interesting historical records are furnished by a male labeled "Cuba/Poey”
and “Loew Coll." and a female with similar labels [both Cambridge], and a male,
"Havana, Cuba” "27.1.'69" [Washington, very old handwritten label, undoubtedly
1869], showing that the species has been in the New World for well over a century.
30. Desmometopa singaporensis Kertész
(Figs. 2, 5)
Desmometopa singaporensis Kertész, 1899, Termész. FuUzetek 22: 194
(Singapore)[Budapest].
. tarsalis Loew (syn., singaporensis); Hendel, 1907, Wien. Ent. Ztg. 26: 242
[but at least Egypt and Aden records refer to varipalpis].
IO
D. tarsalis; Malloch, 1914, Ann. Mus. Nat. Hungar. 12: 309 (male, female)
[Budapest].
D. tristicula Hendel, 1914 (Jan. 27), Suppl. Ent. 3: 96 (Formosa) [Eberswalde].
N. syn.
D. palpalis de Meijere, 1914 (Oct. 15), Tijd. Ent. 57: 251 (Java, Sumatra)
[Amsterdam].
D. tarsalis; de Meijere, 1914 (Oct. 15), Tijd. Ent. 57: 251 (Java, Sumatra;
females).
D. m-nigrum (Zetterstedt) Illingworth, 1926, Proc. Hawaiian Entomol. Soc.
6(2): 224 (Hawaii, det. Aldrich).
. tarsalis (female) and D. palpalis (male); Bezzi, 1928, Diptera Brachycera
and Athericera of the Fiji Islands, p. 162-3 (Fiji; also Fiji, “from onions
imported from Australia”).
. tarsalis; Illingworth, 1929, Proc. Hawaiian Ent. Soc. 7(2): 233
("“Correction” from Aldrich of his earlier identification of m-nigrum).
. palpalis; Malloch, 1934, Insects of Samoa, Pt. VI (Diptera), Fasc. 8: 327-8
(Samoa; fig. of male head and palpus; first to note sexual dimorphism in the
palpi of this species). :
. palpalis; Hennig, 1939, Arb. Morph. Taxon. Ent. Berlin-Dahlem 6: 88-89,
fig. 8 (head of male, side view).
. tarsalis; Hennig, 1941, Ent. Beihefte aus Berlin-Dahlem 8: 177 (Formosa, at
least in part; I have seen the Hokuto specimens).
. palpalis; Bohart and Gressitt, 1951, Bull. Bishop Mus. 204: 46 (Guam).
. palpalis; Hardy, 1952, Proc. Hawaiian Ent. Soc. 14(3): 474 (Hawaii).
singaporensis; [Hardy?], 1972, Proc. Hawaiian Ent. Soc. 21(2): 160 (Correct
name for species known in Hawaiian literature as palpalis, teste Sabrosky).
. palpalis; Sabrosky, 1973, Family 75, p. 2, in A Catalogue of the Diptera of
the Americas South of the United States (Brazil, Puerto Rico).
. singaporensis (syn., palpalis) and D. tristicula; Sabrosky, [1977], Family
Milichiidae, p. 271, in Delfinado and Hardy (eds.), A Catalog of the Diptera of
the Oriental Region.
. tristicula; Hardy and Delfinado, 1980 (June 4), Insects of Hawaii 13: 356,
358 (Hawaii, figs. of head and male genitalia).
. singaporensis (syn., palpalis); Sabrosky, 1980 (July 10) Family
Milichiidae, p. 687, in Crosskey (ed.), Catalogue of the Diptera of the
Afrotropical Region.
lO
|O
lO
|O
ISIDID «IO
|O
|O
|O
lO
Sabrosky: Desmometopa of the World 45
Polished pleural spot small, not including an area of mesopleuron;
fronto-orbital plates relatively narrow (fig. 2); palpus of male broadly expanded,
capitate (fig. 5). |
Male, female. Black, heavily gray microtomentose; cheek yellowish in ground
color; antenna usually black but sometimes Ist and 2nd segments reddish; palpus
partly yellow, extensively so in male but only proximal 1/2 in female; knob of
halter yellow; mid and hind tarsi sometimes yellowish on proximal 2 to 3
tarsomeres.
Frons with velvet black frontal vitta, the interfrontal and fronto-orbital
plates and frontal triangle gray and distinct; each fronto-orbital plate moderately
narrow, especially the lower orbital plate, and almost always with a more or less
distinct break between upper and lower sections, just anterior to foremost upper
orbital bristle (fig. 2); frontal triangle longer than broad at base, its apex about
midway on frons; cheek about 1/2 breadth of 3rd antennal segment and 1/8-1/9
height of an eye, with narrow polished subocular crescent (fig. 5); parafacial —
usually not visible in profile; face weakly concave, vibrissal angle not produced,
about an 80° - 90° angle, lateroventral corner of facial plate dull gray and not
_ warped forward; 3rd antennal segment small in both sexes; palpus gently clavate
in female, but in male elongate and broad, capitate (fig. 5).
Thoracic pleuron densely and extensively gray microtomentose, with small
polished spot on pleuron posterodorsad to fore coxa, no adjoining polished area
anteroventrally on mesopleuron (cf. fig. 25). Fore coxa and femur not elongate.
Costal setae as in varipalpis. Length, 2.5 mm.
Lectotype, female, "Singapore/Bird 1898," "M-nigrum" [Bird label],
"Desmometopa/singaporensis/typus [in red ink] Kert./ det. Kertész," “typus"
[printed in red on large red-bordered label], "tarsalis Lw./ det. Hendel."
Paralectotypes: 6 females, "Singapore/ Bird 1898" [Budapest]; 3 females, same
data [Vienna]. Of the paralectotypes, 5 in Budapest are the narrow-cheeked
species, conspecific with the lectotype; the other four are varipalpis.
Kertész did not state the number of specimens in the type series, nor did he
designate a holotype. The stated range of length (2.3-2.5 mm) and the use of the
plural “die Exemplare"” show that he had at least more than one specimen, and
thus the single example now labeled “typus” is technically not a holotype. It
seems reasonable to conclude that the seven specimens in the Museum at
Budapest bearing identical labels "Singapore/Biré 1898" as published by Kertész,
and standing in the collection under the name label "tarsalis Lw. (singaporensis
Kert.) as revised by Hendel, are all syntypes. All are females, and these are now
before me. Hendel (1907) also referred to "Typen" in the Museum in Vienna, and I
have seen.those three, also females with identical data to those in Budapest, and
here also considered syntypes. Six of the Budapest specimens, including the one
labeled “typus,” are a narrow-cheeked species agreeing with palpalis de Meijere,
and one is a broader-cheeked form agreeing with varipalpis Malloch. The three in
Vienna agree with the latter. I have designated and labeled as lectotype the
specimen in Budapest bearing the label “typus." Another female from Singapore,
collected by Bird, is labeled 1895 and thus cannot be considered a syntype,
although it is possible that it was before Kertész and he overlooked the difference
in date. It is varipalpis. |
There was a strong temptation to designate the one wide-cheeked example in
Budapest as lectotype, which would have saved the name singaporensis for the
species often (e.g., by Hennig 1937)---but not always--called that. However, such
a designation would have been inconsistent with the labeling of the single
specimen as “typus," it would have disagreed with the original description, and it
would have been contrary to the majority of the specimens. The labeling of
"typus" is not a binding consideration under the International Code of Zoological
46 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Nomenclature, because it was not published, but some taxonomists may consider
that such labeling should fix the status of the specimen and I consider it desirable
to avoid that possible argument, as well as to respect the author's choice. In view
of the mixed series, perhaps that “choice” was unintentional, but on the other
hand it may have indicated the choice of an individual that seemed to Hendel
most typical in the type series. Most of the description is generalized and applies
in most particulars to both species, but the characters of 'cheeks very narrow' and
‘antennae black’ apply to the narrow-cheeked species and not to the other,
varipalpis, which has a broader cheek-although not exceedingly so--and partly
reddish antennae, differences that are clearly evident in the type series.
The narrow-cheeked form is that described by de Meijere as palpalis, from
Salatiga, Java (D. van Leeuwen) and Deli, Sumatra (de Bussy). The palpi were
described as “sehr gross, loffelformig.” I have before me, loaned from the
Museum at Amsterdam by Dr. G. Kruseman, two males of the cited data. The one
from Java was labeled "Type" by de Meijere, although not so published, and I here
designate it as lectotype, the other being paralectotype. Three females of the
same species are also present in that collection, labeled tarsalis by Becker
(Pasuruon, Java) and by de Meijere (Semarang, Java, and Deli, Sumatra). The last
two specimens were published by de Meijere as tarsalis at the same time that he
described the males as palpalis.
D. tristicula Hendel was briefly and inadequately described from "#¢", kindly
loaned me for study from Eberswalde by Dr. G. Morge. One specimen is obviously
a female, with genitalia clearly evident. The other, presumably the male referred
to, bears a red label “Typus" but this was not so published and the type series
really consists of two syntypes. The “male” is unrecognizable; it is now headless,
the mid and hind legs are missing, and the abdomen, which has had the distal half
sliced off, appears filled with eggs! Hennig (1941) recorded "1 Typus plus 1" in his
list of the insects of Formosa, but this was a curatorial list and cannot be
considered a definitive nomenclatural act. In other cases, all of Hendel's series
have been marked "Typus", and the lack of such a label on the second specimen is
probably a preparator's error. I hereby designate as lectotype the second
specimen, the female, which is in excellent condition. Dr. Morge also sent 17
other specimens, mostly from H. Sauter's collecting in Formosa, identified as
tristicula, most of which had been recorded by Hennig (1941). Four of these, from
H. Sauter's collecting at Tainan, Nov. 1909 (1 female) and Hokuto, Dec. 1912 (2
males, 1 female) are tristicula, but most of the others are microps.
Unfortunately, the abdomen is missing from each of the available males of
tristicula, but the capitate palpus is characteristic of that sex.
The species that I recognize as singaporensis is nearest varipalpis, and
although males of the two are easily distinguished by the form of the strongly
developed palpi, identification of females is much more difficult, as discussed in
detail under varipalpis. Females of singaporensis have a slightly narrower cheek
and narrower fronto-orbital plates with a distinct break between upper and lower
orbital plates. It must be kept in mind, as noted under varipalpis, that small
males have less strongly developed and less conspicuous palpi, and this can
sometimes be quite deceiving.
Hennig (1939) unfortunately misquoted Malloch as saying that only the
females of palpalis have the enlarged and brightly marked palpi, whereas Malloch
(1934a) had positively stated that such palpi were "characteristic of the male
only" and that females had small palpi as in m-nigrum and ciliata. Probably
Hennig was influenced by his natural acceptance of Malloch's earlier (1927)
statement (erroneous!) that varipalpis was based on a female specimen.
As far as usage is concerned, there has been a great deal of confusion, to
which I too have contributed. The name singaporensis has been applied to both
Sabrosky: Desmometopa of the World 47
broad- and narrow-cheeked species, especially in the female sex in which the two
species are difficult to separate. Because of the confusion and the relatively few
publications involved, there is no overwhelming amount of usage that needs
special consideration. Either choice would have resulted in synonymy. Moreover,
if singaporensis had been restricted to the broad-cheeked form (varipalpis), the
name most commonly used for the narrow-cheeked form, i.e., palpalis, would have
had to be changed anyway as a junior synonym of tristicula. For further
discussion of the confusion, see the introductory paragraphs under “Identification”.
Distribution: Chiefly Old World, and chiefly Oriental and the Pacific Islands.
I can record specimens from the following:
Neotropical: Brazil (Santos, S.P.), Puerto Rico.
Afrotropical: Ivory Coast, Seychelles, South Africa (Transvaal), Uganda.
Oriental (including some chiefly Palearctic countries with Oriental sections):
Afghanistan, Cambodia, China (Szechuan), India (Assam, Bengal), Java, Korea,
Malaya, Pakistan, Philippine Islands, Ryukyu Islands (Okinawa), Singapore, South
Viet Nam, Sri Lanka, Sumatra, Taiwan, Thailand.
Pacific Islands: Bismarck Archipelago (New Britain), Caroline Islands (Merir
Island, Palau Islands, Truk), Fiji, Gilbert Islands (Tarawa Atoll), Guam, Hawaii,
‘Mariana Islands (Saipan), Marshall Islands (Kwajalein), New Hebrides, Solomon
Islands (Guadalcanal, Russell Group), Tahiti, Tonga, Yap.
31. Desmometopa sordida (Fallén)
(Fig. 8)
Madiza sordida Fallén, 1820, Oscinides Sveciae, p. 10 (Sweden) [Stockholm].
Agromyza M atrum Meigen, 1830, Syst. Beschr. 6: 170 (usually cited m-atrum).
Desmometopa (Liodesma) atra Duda, 1935, Natuurhist. Maanblad 24: 25, 38
(Saarland, West Germany) [Berlin]. (Synonymy confirmed).
D. sordida (Fallén)(?Liodesma atra Duda) Hennig, 1937, Milichiidae et
Carnidae, in Lindner, Fliegen Palaeark. Region, Fam. 60a: 43.
Entirely black or dark brown, including knob of halter; cheek with distinct
subocular crescent.
Male, female. Entirely black or dark brown, including palpi, halteres, and all
tarsi. )
Frons subshining black, the dark gray interfrontal and fronto-orbital plates
and frontal triangle distinct; interfrontal plates moderately long, widely
divergent, posterior ends barely overlapping apex of frontal triangle; cheek over
3/5 breadth of 3rd antennal segment and nearly 1/6 height of an eye, with large
rounded subocular crescent (fig. 8); face weakly concave in profile, vibrissal angle
about 90°, not produced; 3rd antennal segment small in both sexes; palpus clavate.
Thoracic pleuron densely brownish microtomentose, including all propleuron
and areas surrounding anterior spiracle, a polished black spot posterodorsad to
fore coxa that only narrowly or not at all encroaches on anteroventral area of
mesopleuron. Fore coxa not elongate, convex, about 3/5 length of fore femur.
Length, 2-2.5 mm.
D. sordida, whose junior synonym m-atrum is type of the genus, is a dark,
nondescript species without particularly distinctive characters. In the Holarctic
Region its black halteres distinguish it. It has apparently not been distributed
widely in commerce as has D. m-nigrum, and published records in the Oriental and
Afrotropical Regions are suspect.
It is widespread in North America and the Palearctic Region. I have seen
numerous specimens from England, Sweden, and Russia (Leningrad Oblast) south
48 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
to Spain and Israel, also Manchuria and Japan.
In the “Catalog of the Diptera of the Oriental Region" (Sabrosky [1977], p.
271), I listed sordida from "India, Indonesia, Philippines” but indicated possible
misidentifications. Up to the present time, I have not seen true sordida from the
Oriental Region. Two specimens from Semarang, Java, August 1905 (Jacobson),
borrowed from the Museum in Amsterdam as sordida, proved to be D. microps
Lamb, and this is a likely species to be confused with sordida.
Likewise, in the “Catalogue of the Diptera of the Afrotropical Region”
(Sabrosky 1980), I listed sordida from "Cameroun, ?Kenya, Tanzania”, but these
records too may now be doubted. The specimen on which the Cameroun record
was based is before me, and it is a female of microps as I now recognize. The
Tanzania record was also based on a female, recorded earlier by me (Sabrosky
1965a), and I suspect that this was also microps, the female being easily confused
with that of sordida. The Kenya record was published by Séguy (1938), and should
be checked for this same possibility.
Through the friendly cooperation of Dr. H. Schumann of the Museum fir
Naturkunde, WHumboldt-Universitat zu Berlin, I received for study the two
specimens on which Duda founded his Desmometopa atra. One is teneral, with
head and thorax collapsed. The other, which I here designate as lectotype, bears
the following labels: "8 8 19, St. Wendel/Rheinl. Duda [printed], Piomadiza n.
gen., atra Duda?, Typus [printed, colored label].". The name labels are in Duda's
handwriting. Duda apparently changed his mind on the generic name and its
status, before publishing. The other specimen, which now becomes a
paralectotype, is labeled "6 8 20, 5a, atra Dudae' [actually a female and so
published], Typus [printed, colored label]." Its locality was published as
“"Habelschwerdt (Schlesien).”
Duda described the face of atra, in contrast to Desmometopa, as "poliert
glanzend" and the frons as “glanzend und unbereift,” hence the name Liodesma.
However, the shining appearance is an artifact. The entire head has been wetted
with a dark, syrupy substance. The specimens are simply the common D. sordida,
and I can confirm the synonymy suggested by Hennig (1937) from his reading of
the description.
32. Desmometopa sp. L
A lone male, MALAYA: Pahang, Tahan River, George V National Park, Nov.
5, 1959 (H.E. McClure, light trap)[Washington], apparently represents a distinct
species, with characters as given in the key, but it will not be described and
named until further material is available. It is tiny (1 mm), with narrow
interfrontal plates and short frontal triangle that together result in an unusually
large M-shaped frontal vitta. The palpus is short clavate and black, and the 3rd
antennal segment is small, only a little larger than the 2nd seqment, both
structures undoubtedly the same in females. The fore coxa is not elongate. The
polished black spot posterodorsad to fore coxa appears to include, as in sordida, a
very narrow anteroventral area on the mesopleuron.
33. Desmometopa nudigena, n. sp.
Tiny dark species of the sordida habitus, but with all tarsi partly yellow, and
cheek lacking a polished subocular crescent.
Male, female. Black, dark gray microtomentose; all tarsi yellow except for
distal segment or two.
Frons with velvet black frontal vitta, the gray interfrontal and fronto-orbital
plates and frontal triangle distinct; interfrontal plates very narrow, practically
Sabrosky: Desmometopa of the World 49
linear, hence the sections of the M-shaped frontal vitta unusually broad, the
plates long, with posterior ends opposite apex of the short frontal triangle which
is virtually coextensive with ocellar tubercle; cheek narrow, 1/4 breadth of 3rd
antennal segment and 1/12 eye height, gray, without polished subocular crescent;
face weakly concave, vibrissal angle an 80° - 90° angle and not produced
anteriorly; lateroventral corner of facial plate flat, gray like rest of plate; 3rd
antennal segment small in female but large in the now headless male (cf. fig. 21);
palpus clavate.
Thorax densely dark gray microtomentose, including entire propleuron and
areas surrounding anterior spiracle; a large polished black spot posterodorsad to
fore coxa and including an elongate-oval anteroventral area of the mesopleuron
(cf. fig. 24). Fore coxa and fore femur ordinary, not elongate. Section of costa
between costal breaks with 8 erect, coarse, black, well-spaced setae. Length,
1.25 - 1.5 mm.
Holotype female and female paratype, GAMBIA: Bakau, Botanical Garden,
Nov. 21, 1977 (Cederholm et al.)[Lund]. Paratypes: GAMBIA: (all, Cederholm et
al.): female, 6 km n. Kartung, Nov. 20, 1977, "swept in very dense forest with
glades” [Lund]; male, female, at road junction to Situ Sinjang, about 2.5 km se.
Kafuta, Mar. 1, 1977 [Lund, Washington]. IVORY COAST: female, Savane a
Imperata, May 5, 1971 (D. Lachaise, "inflorescence de Cussonia") [Paris]. SIERRA
LEONE: Female, Taninahur, Feb. 14, 1925 (E. Hargreaves) [London]. NIGERIA:
female, Ibadan, Dec. 4, 1962 (D.C. Eidt) [Ottawa].
The head of the male was accidentally and irretrievably lost, but not before
it was noted that the 3rd antennal segment was unusually large, in which feature
it resembles magnicornis and philippinensis (cf. fig. 21).
This species is one of a small group characterized by black-brown halteres
and, in the male, by extra large 3rd antennal segment. It is differentiated in the
key from the other species with these features, magnicornis and philippinensis by
its longer frontal triangle, but in these small species the difference does not
appear great. Should there be confusion, however, different combinations of
other characters served to mark these as distinct species, in addition to the length
of the triangle:
nudigena: subgenal setae fine and even, without outstanding bristle; all tarsi
yellowish except for distal segment or two.
philippinensis: 2nd subgenal seta behind the vibrissa bristlelike, longer than
the others; all tarsi yellowish except distally.
magnicornis: subgenal setae fine and even; all tarsi black.
Possibly D. aldabrae belongs in this group also, although the 3rd antennal
segment is only moderately enlarged in the male. Should it be involved in the
possible confusion, it is easily distinguished by almost entirely yellow palpi in both
sexes. The subgenal setae are even and the tarsi are yellowish except distally.
The specific name is a noun in apposition compounded from the Latin nudus,
bare, plus gena, cheek.
34. Desmometopa flavipalpis, n. sp.
Small dark species of the sordida habitus, but males with yellow palpus, and
both sexes with short frontal triangle.
Male, female. Black, except for yellow palpus in male, slightly infuscated at
tips, and basal 1/3 to 1/2 of palpus orange-yellow in females.
Frons subshining, velvet black, interfrontal plates distinct but of moderate
width, the sections of M-shaped frontal vitta broad; frontal triangle short, apex
barely anterior to median ocellus; face weakly concave, the vibrissal angle not
produced forward, about an 80° - 90° angle; cheek narrow, barely over 1/3 breadth
50 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
of 3rd antennal segment and 1/11 eye height, with linear polished subocular
crescent that is slightly wider anteriorly; subgenal setae rather long and
lengthening toward vibrissa; 3rd antennal segment small in both sexes; palpus
short, clavate.
Thorax dark gray microtomentose, including entire propleuron and areas
surrounding anterior spiracle, with large polished black spot posterodorsad to fore
coxa that includes an anteroventral area of the mesopleuron (cf. fig. 24). Fore
coxa not elongate. Length 1.75-2 mm.
Holotype male, allotype, and 4 paratypes (3 males, 1 female), MARSHALL
ISLANDS: Jaluit Atoll, Majurirek Island, Apr. 26, 1958 (J.L. Gressitt, "Hernandia
flowers")[Honolulu]. Other paratypes: MARSHALL ISLANDS: 10 males, Jaluit
Atoll, Jabor Island, Apr. 27 and May 1, 1958 (J.L. Gressitt, two of Apr. 27 labeled
"Crotalaria"), CAROLINE ISLANDS: 2 males, | female, Ulithi Atoll, Falalop
Island, April 30, 1952 (J.W. Beardsley); female, Lamotrek Atoll, Lamotrek Island,
Feb. 5, 1953. PALAU ISLANDS: female, Angaur Island, May 1, 1954 (J. W.
Beardsley), NEW HEBRIDES: male, Efate, Vila, 0-100 m, Feb. 1969 (N.L.H.
Krauss). [Most paratypes in Honolulu, paratypes in Washington; New Hebrides
paratype in Washington].
This species is similar to others of the sordida group in the Oriental and
Pacific areas, but it can be distinguished by the combination of characters used in
the key. Two noteworthy features are the very short frontal triangle and the
conspicuous yellow palpi of the males. Females are much less distinctive because
the palpi are heavily infuscated distally and apparently sometimes entirely black.
The specific name is an adjective compounded from the Latin flavus, yellow,
and palpus, feeler.
Two females from the Philippines have not been included in the type series,
but they appear to be this species: Samar, Osmena, May 23, 1945 (K. L. Knight,
at light), and Calicoan Island, July 27, 1945 (F.F. Bibby, “from dead land crab")
[Washington].
35. Desmometopa srilankae, n. sp.
Tiny species near ciliata, but with bilobed polished black pleural spot.
Male, female. Chiefly black; palpus yellowish on basal half; all tarsi yellow
except for several distal segments; knob of halter black.
Frons with velvet black M-shaped frontal vitta, the arms of the M broad,
interfrontal plates long and slender, posterior ends at or posterior to level of
hindmost orbital bristles; frontal triangle short, apex barely before median
ocellus; cheek 1/3 breadth of 3rd antennal segment and 1/9 height of an eye, gray,
with distinct but narrow subocular crescent, 2nd subgenal seta behind vibrissa
more or less well developed; face weakly concave in profile, vibrissal angle not
produced, about an 80° angle, and lateroventral corner of facial plate flat and
dull, not polished; 3rd antennal segment small, only little larger than 2nd; palpus
clavate.
Thorax dark gray microtomentose; pleuron chiefly gray, including entire
propleuron and areas surrounding anterior spiracle, with large, bilobed (cf. fig.
23), polished black spot posterodorsad to fore coxa, including an anteroventral
area of mesopleuron. Fore coxa and fore femur not elongate in male. Section of
costa between costal breaks with few coarse setae, 6-7 in number. Length, 1.5
mm.
Holotype male, allotype, and 3 female paratypes, SRI LANKA: Kandy
District, Udawattakele, 1800 ft., Nov. 19, 1976 (G.F. Hevel, R.E. Dietz, S.
Karunaratne, D.W. Balasooriya)[Washington, paratype in Colombo]. Other
paratypes: SRI LANKA: 2 females, Northwest Province, Bangadeniya, 4 mi. nne.
Chilaw (Brinck & Cederholm, on flowers)[Lund, from the Lund University Ceylon
Expedition 1962].
Sabrosky: Desmometopa of the World 51
One male, PHILIPPINES: Luzon, La Trinidad, May 1914 [Helsinki] appears to
belong here but it is.in poor condition and decision on its identity must await
better material from those islands.
The bristlelike 2nd subgenal seta, the bilobed pleural spot, and the unusually
sparse setae on the costa between the costal breaks will spot this species as near
ciliata.
In the holotype, both interfrontal plates are interrupted midway, but they are
continuous in the other specimens and the interruption is undoubtedly an aberrant
condition.
The specific name is a noun in the genitive case, from the name of the
country Sri Lanka.
36. Desmometopa propeciliata, n. sp.
Tiny species near ciliata and srilankae, differing from the latter in a
combination of characters as shown in the key, and from ciliata in having
brown-black halter and narrower cheek with linear subocular crescent.
Male, female. Chiefly black; 3rd antennal segment orange-yellow on
basoventral half in male; palpus chiefly yellow in male, broadly infuscated distally
in female; all tarsi yellowish toward base.
Frons velvet black, frontal vitta delineated by distinct but slender
interfrontal and fronto-orbital plates, the frontal triangle short, apex not
exceeding median ocellus; cheek of moderate width, 1/3 breadth of 3rd antennal
segment and 1/12 height of an eye; 2nd subgenal seta behind vibrissa a rather
strongly developed bristle, suggestive of ciliata (cf. fig. 11); face weakly concave
in profile with vibrissal angle not produced, about an 80° angle, and latero-ventral
corner of facial plate dull gray and flat; 3rd antennal segment small, little longer
than 2nd segment; palpus clavate.
Thorax dark brownish gray microtomentose; pleuron chiefly gray, including
entire propleuron and areas surrounding anterior spiracle, with large polished
black spot posterodorsad to fore coxa, and including narrow anteroventral area of
mesopleuron, the polished spot not bilobed (cf. fig. 24). Fore coxa not elongate.
Section of costa between costal breaks with 7 coarse and well spaced setae, each
much longer than diameter of costa. Length, 1.5 mm.
Holotype male, allotype, and 3 paratypes (male, 2 females), MALAYA:
Pahang, Tahan River, George V National Park, Nov. 5, 1959 (H.E. McClure, light
trap)[Washington]. Other paratypes: THAILAND: female, Nonthaburi, Dec. 20,
1958 (Manop)[Washington]. JAVA: 3 males, 1 female, Bogor, Apr.-May 1954
(A.H.G. Alston)[London].
This species is closest to srilankae and the combination of characters for
each is shown in the key. The developed subgenal bristle and long, coarse,
well-spaced setae on costa between the humeral and subcostal breaks clearly
relate the species to ciliata.
The specific name is an adjective from the Latin prope, near, plus ciliata, the
name of a similar species.
aT, Desmometopa maqnicornis, n. sp.
(Fig. 21)
Entirely black, narrow cheek lacking a subocular crescent, and male with
exceptionally large 3rd antennal segment.
Male, female. Entirely black to brown-black, including palpi, halteres, and
tarsi.
52 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Frons with velvet black frontal vitta, the gray interfrontal and fronto-orbital
plates and frontal triangle distinct; inter-frontal plates long, 2/3 length of frons
and extending posteriorly to level of apex of the approximately equilateral frontal
triangle, the plates widely divergent and interval between them wider than that
between one of them and adjacent fronto-orbital plate; cheek narrow, 1/3 breadth
of 3rd antennal segment and 1/10 height of an eye, entirely gray without visible
subocular crescent; face weakly concave, vibrissal angle about an 80° angle, not
produced, and lateroventral corner of facial plate not developed; 3rd antennal
segment of male exceptionally large, 2 to 3 times the length and breadth of 2nd
segment and extending to lower margin of face (fig. 21); palpus small, clavate.
Thoracic pleuron densely dark gray microtomentose, including entire
propleuron and areas surrounding anterior spiracle; a large polished black spot
posterodorsad to fore coxa and including anteroventral area on mesopleuron (cf.
fig. 24). Fore coxa convex, short. Length, 1.5 mm.
Holotype male, allotype, and 6 paratypes (1 male, 5 females), NIGERIA:
Ibadan, Gambani Forest, Feb. 1965 (R.W. Williams, “reared cacao pods")
[Washington]. Other paratypes: NIGERIA: female, Ibadan, Jan. 7, 1963 (D.C.
Eidt, Malaise trap)[Ottawa]. IVORY COAST: female, ‘Lamto’, Frange,
Afrayomum, Mar. 20, 1971 (D. Lachaise) [Paris].
This entirely black species is easily distinguished by the absence of a
subocular crescent on the cheek, and by the exceptionally large 3rd antennal
segment of the male. The reared series was obviously mounted from fluid and is
paler in color than one would expect. The paratype from a Malaise trap is fully
colored and is the basis of the color description. See discussion at end of nudigena
for separation of the three species with black-brown halteres and extra large 3rd
antennal segments in the male, nudigena, philippinensis, and magnicornis.
The specific name is an adjective referring to the large antennal segment.
38. Desmometopa sp. M
A single female from TAIWAN (as Formosa): Chipun, July 1912 (H.
Sauter)[Eberswalde], identified in the collection as D. tristicula, appears to
represent a new species near sordida but with narrow cheeks and sublinear
polished subocular crescent. The interfrontal and fronto-orbital plates are fairly
broad although nowhere near the pattern in interfrontalis. A relatively strong
subgenal bristle is present, although not as strongly developed as in ciliata (cf. fig.
11). At least the first two tarsomeres are yellowish in all tarsi. The 3rd antennal
segment is small, which is normal for females. The fore coxa is a little longer
than usual, and it is possible that the male will be found to have elongate fore
coxa, although not necessarily so. The polished black spot posterodorsad to the
fore coxa is bilobed and includes an anteroventral area on the mesopleuron (cf.
fig. 23).
39. Desmometopa philippinensis, n. sp.
Tiny species near ciliata, but with large 3rd antennal segment in both sexes.
Male, female. Chiefly black or black-brown; all tarsi yellowish except
distally; knob of halter brown.
Frons with broad velvet black frontal vitta distinctly delineated by
interfrontal and fronto-orbital plates and short frontal triangle, apex of latter not
reaching middle of frons; cheek less than 1/2 breadth of 3rd antennal segment and
1/8 height of an eye, uniformly gray, without polished subocular crescent; 2nd
subgenal seta developed bristlelike (cf. fig. 11); face only weakly concave, the
vibrissal angle not produced, an 80° - 90° angle, and lateroventral corner of
Sabrosky: Desmometopa of the World 53
facial plate flat and dull; 3rd antennal segment in both sexes larger than usual,
and larger in male than in female, in male similar to but not as extreme as in fig.
21; palpus clavate.
Thoracic pleuron brownish gray microtomentose, including entire propleuron
and areas surrounding anterior spiracle, with large polished black spot
posterodorsad to fore coxa that includes an anteroventral area on mesopleuron,
anterior margin of spot approximately straight, not bilobed (cf. 24). Fore coxa of
male not elongate. Section of costa between the costal breaks with few (8-9)
coarse and well-spaced setae. Length, 1.5 mm.
Holotype male, allotype, and a female paratype, PHILIPPINES: Manila
(Robert Brown)[Washington].
The large antennae will distinguish this species in the ciliata group. See
discussion at end of nudigena. Unlike the other species with black-brown halteres
and extra large 3rd antennal segments in the male, nudigena and magnicornis, this
species has a developed subgenal bristle, second behind the vibrissa, and
outstanding in the subgenal row.
The specific name is an adjective referring to the Philippine Islands.
40. Desmometopa sp. N
Two females, and possibly a third, appear to represent a new species but it
will not be named at this time. It is one of several tiny species "near" sordida in
the sense of generally dark appearance, black palpi and black halteres. The large
polished black pleural spot posterodorsad to the fore coxa includes an
anteroventral area of the mesopleuron (cf. fig. 24). The 3rd antennal segment is
small and the fore coxa short, but these features are usual in females and do not
necessarily indicate the appearance of the males.
MALAYA: Two females, Pahang, Tahan River, George V National Park, Nov.
5, 1959 (H.E. McClure, light trap), and Perak, Pulau Panghor, Apr. 1, 1959 (R.
Traub, light)[both, Washington]. One female, PHILIPPINES: Port Bauge, Jan.
1915 [Helsinki] is not in good condition but is tentatively associated here.
41. Desmometopa aldabrae, n. sp.
Small species with palpus almost entirely yellow in both sexes.
Male, female. Black, with predominantly yellow palpus, slightly
infuscated at extreme apex; knob of halter brownish; tarsi yellow except for distal
tarsomere or two.
Frons relatively broad, nearly square, the interfrontal plates, broad
fronto-orbital plates, and frontal triangle gray and distinct, the sections of the
M-shaped frontal vitta relatively narrow; frontal triangle moderately long, its
apex nearly midway on the frons and well anterior to the posterior ends of
interfrontal plates; cheek narrow, no more than 1/3 breadth of 3rd antennal
segment and 1/8 the height of an eye, subocular crescent absent or indistinct;
face weakly concave, vibrissal angle an 80° — 90° angle, not produced anteriorly;
3rd antennal segment small in female, moderately large in male; palpus clavate,
approximately same in both sexes.
Thorax heavily gray microtomentose, propleuron and area _ surrounding
anterior spiracle entirely so, a small polished black spot posterodorsad to fore
coxa that barely or not at all encroaches on the mesopleuron (cf. fig. 25). Fore
coxa and femur of male ordinary, not elongate. Costa between costal breaks with
8-9 fine and erect dorsal setae. Length, 1.25-1.5 mm.
Holotype male, ALDABRA: South Island, Flamingo Pool, Jan. 21-22, 1968 (B.
Cogan, A. Hutson), and allotype, Dune Jean-Louis, Mar. 13-20, 1968 (Cogan and
54 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Hutson, at light)[London, collected on the Aldabra Atoll Royal Society Expedition
1967-68].
This is a distinctive little species, dark but lightened by the predominantly
yellow palpi in both sexes.
The specific name is a noun in the genitive case, from Aldabra.
42. Desmometopa kandyensis, n. sp.
Subshining velvet black frontal vitta, short and equilateral frontal triangle,
and small polished black pleural spot. :
Male, female. Black, heavily gray microtomentose; knob of halter yellow;
tarsi somewhat yellowish basally in female.
Frons with M-shaped frontal vitta subshining velvet black viewed from any
angle, the interfrontal and fronto-orbital plates and frontal triangle gray
microtomentose and sharply distinct; interfrontal plates long, reaching level of
uppermost fronto-orbital bristles and opposite apex of very short frontal triangle
which is virtually coextensive with ocellar tubercle; cheek narrow, little over 1/3
breadth of 3rd antennal segment and 1/9 eye height, with narrow polished
subocular crescent; face moderately concave in profile, vibrissal angle produced
to a 45° angle and lateroventral corner of facial plate shining black and warped
forward; 3rd antennal segment small in both sexes; palpus gently clavate in both
sexes.
Thoracic pleuron heavily gray microtomentose, including entire propleuron
and areas surrounding anterior spiracle, only a small polished black spot postero-
dorsad to fore coxa, not at all encroaching on mesopleuron (cf. fig. 25). Fore coxa
slightly elongate in male, but fore femur not so. Abdominal tergum 5 unusually
long, longer than 3 and 4 combined; sternum 5 likewise elongate, much longer than
broad and longer than sternum 4, with numerous discal setae (40-50).
Length, 1.5 mm.
Holotype male, allotype, and 2 male paratypes, SRI LANKA: Kandy District,
Udawattakele, 1800 ft., Nov. 19, 1976 (G.F. Hevel, R.E. Dietz, S. Karunaratne,
D.W. Balasooriya)[Washington, one paratype in Colombo].
The combination of velvet black frontal vitta and short frontal triangle will
separate this species from all but gressitti, from which it is easily distinguished by
the several characters noted in the key. Few species in the genus have the pleural
spot so restricted, not encroaching on or including an anteroventral area on the
mesopleuron.
The specific name is an adjective based on the name Kandy District.
43. Desmometopa gressitti, n. sp.
(Fig. 4)
Frontal triangle short, polished pleural spot large, and both halter knob and
tarsi infuscated.
Male, female. Black, heavily gray to brown-gray microtomentose, halter
knob and all tarsi infuscated.
Frons with frontal vitta subshining velvet black, with long and distinct
interfrontal plates, their posterior ends at or posterior to level of uppermost
orbital bristles and opposite apex of short frontal triangle, which is barely if at all
in advance of median ocellus; cheek narrow, 2/3 breadth of 3rd antennal segment
and less than 1/8 height of an eye, with narrow polished subocular crescent; face
deeply concave in profile, the vibrissal angle produced anteriorly to a 45° angle,
and lateroventral corner of facial plate shining and warped forward beyond
vibrissal angle; 3rd antennal segment small in both sexes; palpus clavate, small in
female, but conspicuously broad and flat in male (fig. 4).
Sabrosky: Desmometopa of the World 55
Thoracic pleuron heavily gray microtomentose, including entire propleuron
and areas surrounding anterior spiracle, with large polished black spot postero-
dorsad to fore coxa that includes an elongate-oval anteroventral area on
mesopleuron (cf. fig. 24). Fore coxa and fore femur slightly elongate in male, the
former nearly 3 times as long as broad. Abdominal tergum 5 of male not
elongate, barely longer than tergum 4; sternum 5 large, approximately square,
with numerous discal setae (40-45). Length, 2-2.25 mm; occasional males as
small as 1.5 mm.
Holotype male, allotype and 16 paratypes (10 males, 6 females), MARSHALL
ISLANDS: Jaluit Atoll, Jabor Island, Apr. 25 (allotype), 26, 27, and May 1
(holotype), 1958 (J.L. Gressitt)[Honolulu]. Other paratypes [Honolulu except as
noted]: MARSHALL ISLANDS: 21 males, 5 females, Jaluit Atoll, Majurirek
Island, Apr. 26, 1958 (J.L. Gressitt; 4 labeled “Hernandia flowers"); 2 males, |
female, Jaluit Atoll, Pinlep Island, Apr. 25, 1958 (Gressitt), CAROLINE
ISLANDS: male, Kusaie Island, Matanluk (Yepan), 16 m, Jan. 23, 1953 (Gressitt,
light trap); female, Ponape Island, s. of Nanponmal, Jan. 17, 1953 (J.F.G. Clarke);
2 females, Truk, S. Valley Mt. Tonaachau, Moen, Apr. 2, 1949 (R.W.L. Potts; one
labeled “ex papaya log"; 2 males, 1 female, Ulithi Atoll, Falalop Island, Apr. 30,
1952 (J.W. Beardsley). GILBERT ISLANDS: Butaritari Atoll, Butaritari Island,
Dec. 1957 (N.L.H. Krauss). SOLOMON ISLANDS: 4 males, Guadalcanal, 1944
(C.0. Berg)[Washington]. NEW HEBRIDES: 6 males, 3 females, Efate Island, Vila,
0-100 m, Feb. 1969 (N.L.H. Krauss)[Washington]; 6 males, same locality, Feb.
1970 (N.L.H. Krauss)[London].
I have also seen a number of other specimens that duplicate the above
records, but their poor condition prevents their inclusion in the type series. One
that does add slightly to the known distribution is a male from the New Hebrides,
Espiritu Santo, Sept. 1944 (K.L. Knight)[Washington]. One male from Australia,
Northern Territory, Darwin, Sept. 1908 (Lichtwardt)[Eberswalde] is possibly this
species, but the halter knob is quite yellowish, possibly the result of the teneral
condtion of the specimen.
The nearest relative appears to be flavipalpis, which occurs on some of the
same islands. The two species share the same combination of short frontal
triangle and infuscated tarsi and knob of halter, but they differ in the color and
shape of the palpus. The difference in color of the palpus, all black in qressitti
and partly (female) to chiefly (male) yellow in flavipalpis, might be denigrated as
possibly mere color variation, but the palpal shape is certainly more significant.
In males of qressitti, most noticeable in average to large specimens, the palpi are
very broad and flat (fig. 4), whereas in flavipalpis they are gently clavate, as in
the female.
I dedicate this species to the memory of the collector, J. Linsley Gressitt, my
friend of many years, entomologist extraordinary in the Pacific area, who
perished in a plane crash in China.
44. Desmometopa saquaro, n. sp.
(Fig. 22)
Chiefly polished pleuron, with narrow stripe of gray microtomentum dorsally
on mesopleuron behind anterior spiracle; in male, fore coxa and femur elongate,
raptorial in appearance.
Male, female. Black; knob of halter yellow; basal tarsomere at least partly
yellow on all legs.
Frons gray microtomentose from most angles of view, obscuring the
interfrontal plates which are discontinuous, a series of shining spots about bases
of interfrontal setae; frontal triangle only slightly extended anterior to median
56 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
ocellus; cheek about 2/3 breadth of 3rd antennal segment and 1/6 eye height, with
polished subocular crescent of moderate width; parafacial visible in profile; face
deeply concave in profile, the vibrissal angle produced to a 45° angle,
lateroventral corner of facial plate shining black and warped forward even beyond
vibrissal angle; 3rd antennal segment small in both sexes; palpus clavate, in male
very broad and flat, as in fig. 4 but longer, and at rest projecting even beyond the
antennae.
Thoracic pleuron chiefly polished, including entire propleuron and most of
meso- and sternopleuron, the mesopleuron gray microtomentose dorsally and
posteriorly, a narrow dorsal stripe reaching to anterior spiracle. Fore leg
raptorial in appearance in male, fore coxa and fore femur greatly elongate (fig.
22), the former about 4 times as long as broad and its apex approximately opposite
base of wing, fore femur 1.6 times as long as mid femur, somewhat incrassate,
with anteroventral and posteroventral rows of short, even, straight spines or
spinelike bristles, the postero-ventral weak; fore coxa and fore femur of ordinary
size in female, neither elongated nor enlarged. Length, 1.5-2.5 mm.
Holotype male, allotype, and 13 paratypes (6 males, 7 females), ARIZONA:
Pima Co., Saguaro National Monument (F.J. Santana, “ex rotting Saguaro"),
collected Mar. 10-June 25, 1960, emerged in laboratory at Tucson, Mar. 18-July
8[Washington, paratypes at Tucson]. Other paratypes: ARIZONA: female,
Tucson, Aug. 8, 1937 (O. Bryant)[San Francisco]. CALIFORNIA: male, Andreas
Canyon, Palm Springs, Mar. 11, 1955 (W.R.M. Mason)[Ottawa]; male, Morongo
Valley, Oct. 5, 1934 (A.L. Melander)[Washington].
In addition, but not part of the type series because of teneral condition, I
have seen a long series from CALIFORNIA: Los Angeles Co., San Dimas Canyon,
Apr. 16, 1958, reared June 11, 1958 (R.E. Ryckman, ex Opuntia)[Loma Linda and
Washington], and one male, ARIZONA: Maricopa Co., Wickenburg, Aug. 1950
(H.K. Gloyd, light)[ Washington].
The raptorial fore legs are unlike most other Desmometopa. The nearest
species is melanderi, and I am a little uncertain about their relationship. Both
have been collected in San Dimas Canyon. Aside from the gray postspiracular
stripe, however, there are a few tangible differences: the palpi in saquaro are
definitely longer and broader, the fore coxa and fore femur are longer, but the
spine rows on the femur are weaker than in melanderi, and the tarsi are yellow.
The specific name is a noun in apposition from the common name of the giant
cactus from which the holotype and topotypic specimens were reared.
45. Desmometopa tarsalis Loew
(Figs. 18, 26)
Desmometopa tarsalis Loew, 1866, Berl. Entomol. Ztschr. (1865) 9: 184 (Cent. 6,
no. 96) (Cuba)[Cambridge].
Platophrymyia nigra Williston, 1896, Trans. Entomol. Soc. London 1896: 426
(St. Vincent)[London](Synonymy by Sabrosky 1973).
D. tarsalis; Bohart and Gressitt, 1951, Bull. Bishop Mus. 204: 99(Guam).
Desmometopa sp.; Hardy, 1952, Proc. Hawaiian Entomol. Soc. 14: 474(Hawaii).
D. tarsalis; Hardy and Delfinado, 1980, Insects of Hawaii 13 (Diptera
Cyclorrhapha III): 357-8, figs.
Chiefly polished pleuron with gray stripe to anterior spiracle, gray frons, and
normal (not elongate) fore coxa and fore femur.
Male, female. Black; knob of halter yellow; mid and hind tarsi except distal
tarsomere or two, and usually basal tarsomere of fore leg, yellow.
Sabrosky: Desmometopa of the World 57
Frons with interfrontal and fronto-orbital plates and frontal triangle distinct
but most of the M-shaped frontal vitta dull, gray microtomentose viewed from
most angles, only narrow, long-oval velvet black spots flanking the frontal
triangle; cheek narrow, 2/5 breadth of 3rd antennal segment and 1/9 eye height,
with moderately narrow polished subocular crescent (fig. 18); face deeply concave
in profile, vibrissal angle produced anteriorly to a 45° angle, lateroventral corner
of facial plate shining black and warped forward even beyond vibrissal angle; 3rd
antennal segment small in both sexes; palpus gently clavate, not enlarged in male.
Thoracic pleuron chiefly polished, especially propleuron ventrally and
mesopleuron chiefly, the latter gray microtomentose posteriorly and dorsally, the
gray extending anteriorly to anterior spiracle (fig. 26); typically the sternopleuron
chiefly gray with large polished spot on middle so that the pattern of gray
microtomentum is that of a thick U, open posteriorly. Fore coxa and fore femur
not elongate, in both sexes short and not raptorial. Length, 1.5-2 mm.
The characters given in the key will serve to distinguish the species. It keys
near saguaro, but the two are not necessarily related: the development of
raptorial front legs in that species makes it obviously distinct from tarsalis.
Loew described tarsalis from ‘male and female’, without recording the
number of specimens. Through the kind cooperation of Norman E. Woodley, I
received for study from the Museum of Comparative Zoology at Harvard
University four specimens that I accept as the type series, glued on two card
points, each labeled with a small silver square [meaning Cuba, collected by
Gundlach], an old printed label "Loew Coll.”", and a red MCZ label "Type 13443”.
One of the points, with two females, also has a label, "tarsalis m.”, apparently in
Loew's handwriting. The other point has a male and a female, and I have labeled
and here designate the male as the lectotype. The holotype of P. nigra was
studied at the British Museum (Nat. Hist.) some years ago.
This is a widely distributed, yet also widely misidentified, Neotropical species
that has been transported to Hawaii, and to Wake Island and the South Pacific.
Most of the South Pacific records are from the end of World War II or later, and
could have been associated with the movements of American military forces to
and among the islands. However, at least some introductions may have occurred
earlier; Bohart and Gressitt (1951) found it to be "one of the commonest flies on
Guam” in 1945.
Distribution (confirmed records, after revision):
Nearctic: Arizona, Texas.
Neotropical: Mexico (13 states from Baja California and Tamaulipas south to
Yucatan), Guatemala, Belize, El Salvador, Nicaragua, Honduras, Costa Rica,
Panama, Colombia, Ecuador, Venezuela, Guyana, Tobago, Grenada, St. Vincent,
Barbados, St. Lucia, Dominica, Montserrat, Virgin Islands, Puerto Rico, Bahamas,
Dominican Republic, Cuba, Jamaica.
Pacific: Galapagos, Hawaii, Wake Island, Marianas (Guam, Saipan, Tinian),
Fiji, Solomons (Guadalcanal).
Misidentifications: tarsalis of European authors, at least of records from
Europe, is usually varipalpis, of the material I have seen.
Sabrosky's (1965b) tarsalis in the Nearctic Catalog refers chiefly to new
species described in this paper, except for Arizona and Texas records in part.
Johnson's (1913) record of tarsalis from Biscayne Bay, Fla. (Mrs. Slosson)
actually refers to Milichiella sp. near cinerea (Coquillett).
Bezzi’s (1928) record of tarsalis from Fiji was based on females of
singaporensis. [I have, however, seen other material of true tarsalis from Fiji].
Malloch's (1914) tarsalis from Formosa is singaporensis, from the specimens
in the Museum at Budapest. Another female, Takao, Formosa, April 17, 1907, not
published by Malloch but apparently identified by him, is microps.
58 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
46. Desmometopa nearctica, n. sp.
Velvet black frontal vitta, chiefly polished propleuron, stripe of gray
microtomentum across dorsal edge of mesopleuron to anterior spiracle.
Male, female. Black; knob of halter yellow; mid and hind tarsi with 2 to 3
proximal tarsomeres yellow, basal tarsomere on fore tarsus sometimes yellowish,
at least toward base.
Frons with M-shaped frontal vitta subshining velvet black and the gray
interfrontal and fronto-orbital plates and frontal triangle distinct; interfrontal
plates strong and moderately long, extending posteriorly to level of foremost
upper orbital bristles; frontal triangle moderately long, apex at or slightly
anterior to level of posterior ends of interfrontal plates; cheek narrow, 1/2
breadth of 3rd antennal segment and 1/7 the eye height, with polished subocular
crescent that is wider anteriorly and continuous with a polished, sometimes
narrowly visible parafacial; face deeply concave, vibrissal angle produced
anteriorly to a 45° angle, the latero-ventral corner of facial plate shining black
and warped forward so as to exaggerate the vibrissal angle; 3rd antennal segment
small in both sexes; palpus gently clavate, not enlarged in male.
Thoracic pleuron predominantly polished, including propleuron (except narrow
dorsal strip) and much of mesopleuron, latter with gray stripe of microtomentum
along posterior and dorsal margins up to anterior spiracle (cf. fig. 26);
sternopleuron gray microtomentose above and below, broadly polished centrally,
often with vertical gray stripe. Fore coxa and fore femur short, not elongate in
male. Length, 1.5 mm. He
Distribution: California to Georgia, north to Kansas and New York.
Holotype male, allotype, and 2 male paratypes, CALIFORNIA: Joshua Tree
National Monument, Quail Springs, Oct. 5, 1934 (A.L. Melander)[Washington].
Other paratypes [Washington except as noted}: CALIFORNIA (all A.L. Melander
except Coachella specimen): female, Riverside Co., Whitewater, near Palm
Springs, Oct. 27, 1934; 3 females, Mill Creek, San Bernardino Mts., Aug. 17, 1952;
female, Seven Oaks, sw. San Bernardino Co., July 28, 1953; female, Joshua Tree
National Monument, May 18, 1946; male, Mountain Home Canyon, w. side San
Bernardino Mts., Aug. 9, 1948; male, San Diego Co., Borrego Desert, Tubb
Canyon, w. edge of Anza-Borrego State Park, Nov. 9, 1945; female, Coachella,
Nov. 20, 1930 (D.G. Hall, reared from grass). ARIZONA: 3 females, Maricopa
Co., Buckeye, July 15, 1960 (Ed Schulz, Steiner lure); female, Portal, June 5-9,
1972 (W.W. Wirth, Malaise trap); 2 males, 1 female, Douglas, Aug. 8, 1955 (R.R.
Dreisbach)[East Lansing]. UTAH: male, Uintah Co., Bonanza, July 11, 1974 (G.E.
Bohart, Tamarix). TEXAS: 2 males, 9 females, Big Bend National Park, various
localities, May 1-22, 1959 (J.F. McAlpine, W.R.M. Mason)[Ottawa]; 3 females, Big
Bend National Park, Boquillas Canyon, June 20, 1953 (W.W. Wirth). MEXICO:
male, female, Nuevo Leén, Vallecillo, June 2-5, 1951 (P.D. Hurd)[Berkeley].
GEORGIA: 3 females, Tifton, Sept. 24, Oct., and Oct. 16, 1896. KANSAS: 2
females, Manhattan, Apr. 9, 1934 (C.W. Sabrosky) and Aug. 1945 (N.L.H. Krauss);
male, Douglas Co., Oct. 4, 1937 (H.M. Smith); 2 males, Atwood, July 23, 1954
(W.L. Downes)[Lansing]. IOWA: male, female, Des Moines, May 17, 1951 (A.H.
Sturtevant), NEW YORK: male, female, Cold Spring Harbor, Long Island,
August. DISTRICT OF COLUMBIA: Washington, Aug. 23, 1907 (W.L. McAtee).
A few specimens from Colesville, Md. (W.W. Wirth) and Chittenango, N.Y.
(D.J. Peckham)[Washington] are puzzling. The frontal vitta is slightly gray
microtomentose and thus suggestive of tarsalis, but the localities are far removed
from the known range of that species. All specimens available from the two
Sabrosky: Desmometopa of the World 59
localities are females, so male genitalia cannot be checked. A different species
may be involved, but for the present the specimens are considered here as odd
variants of nearctica.
The specific name is an adjective referring to the Nearctic Region.
47. Desmometopa argentinica, n. sp.
Agreeing with nearctica in all particulars except proportion of width of
subocular crescent to width of cheek (see key), the crescent more evenly rounded
throughout, and cheek slightly wider.
Holotype male, allotype, and 5 paratypes (3 males, 2 females), ARGENTINA:
Salta, Urundel, Feb. 8-12, 1949 (M. Aczél)[Tucuman]. Other paratypes:
ARGENTINA [all Tucumén]: male, Jujuy, Sierra Zaple, Jan. 30, 1949 (M. Aczél); 8
males, 4 females, Santiago del Estero, Monte Potrero, Apr. 13, 1952 (A. Willink).
PERU: female, Iquitos, Mar.-Apr. 1931 (R.C. Shannon)[Washington].
In addition to these I have a female from Urundel and 4 males, 10 females
from Monte Potrero that are too teneral to include in the type series.
This species is extremely close to nearctica, and like that species it is also
very similar to tarsalis, differing in having subshining velvet black frontal vitta.
The proportion of width of subocular crescent to width of cheek is obvious in fully
mature specimens. Unfortunately, in teneral specimens the collapse of the cheek
affects the lower microtomentose portion and narrows it so that the subocular
crescent appears over 1/2 the width of the cheek and thus agreeing with
nearctica. Most available specimens of argentinica are somewhat teneral. The
same tendency in nearctica does no harm because it merely exaggerates the
characteristic proportion of crescent to cheek in that species.
The specific name is an adjective derived from the name of the country of
origin of the type series.
48. Desmometopa sp. 0
A single female undoubtedly represents a distinct species, but in the absence
of additional material and males it is left unnamed. The extensively polished
pleuron and black halter will distinguish it from other species. The pleuron is
microtomentose only on the posterior slope, behind the sterno- and pteropleuron.
The vibrissal angle is not produced anteriorly. The lateroventral corner of the
facial plate is shining black as in the subgenus Platophrymyia, but not warped
forward. The head structure and black halter suggest sordida, but of course the
polished pleuron is quite unlike that heavily microtomentose species. The 3rd
antennal segment is small, as usual in females. The fore coxa is slightly longer
than usual in females, and this may indicate an elongate fore coxa in the male of
the species.
Female, MEXICO: Cuernavaca, July 1965 (N.L.H. Krauss) [Washington].
49. Desmometopa stilbopleura, n. sp.
Predominantly polished black pleuron, lemon-yellow knob of halter, and mid
and hind tarsi with proximal 2 to 3 tarsomeres yellow.
Female. Black; knob of halter lemon yellow; mid and hind tarsi with proximal
2 to 3 tarsomeres yellow.
Frons with frontal vitta gray microtomentose anteriorly and centrally,
broadly velvet black on upper 2/5, on each side of frontal triangle, and anteriorly
60 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
mesad of the fronto-orbital plates; interfrontal and fronto-orbital plates and
frontal triangle strong and distinct; frontal triangle long, apex midway on frons;
cheek moderately narrow, 1/2 breadth of 3rd antennal segment and about 1/7 eye
height, with polished subocular crescent that broadens anteriorly and continues as
narrow polished parafacial visible in profile; face deeply concave, the vibrissal
angle strongly produced to a 45° angle, accentuated by shining black lateroventral
corner of facial plate which is warped forward beyond vibrissal angle; 3rd
antennal segment small; palpus clavate, large, nearly as broad as 3rd antennal
segment. |
Thoracic pleuron predominantly polished anterior to pleural suture, including
propleuron and all but narrow margins on mesopleuron and sternopleuron. Fore
coxa slightly longer than usual for females, and this may indicate an elongate fore
coxa in the male of the species. Length, 2.5-3(holotype) mm.
Holotype and 2 paratypes, all females, BRAZIL: S@o Paulo, Nova Teutonia,
300-500 m (F. Plaumann), one paratype Sept. 1965, the others Nov. 1962 [Ottawa,
paratype in Washington].
This is such a distinctive species that I have named it even in the absence of
males. The microtomentum on the frons is more limited than usual, but it is so
consistent in these specimens that I judge it to be characteristic of the species.
Typically, in species with dull frons, the gray microtomentum is heavier and more
extensive than in this species, completely covering the frons except for a usually
elongate-oval velvet black area along each side of the ocellar tubecle. The
breadth of the palpus suggests that in the male the palpus will be broadly
expanded and flattened (as in fig. 4).
The specific name is a noun in apposition compounded from the Greek stilbo,
shine, plus pleura, side.
50. Desmometopa melanderi, n. sp.
Pleuron polished anterior to pleural suture; frons chiefly dull; fore coxa and
fore femur of male elongate, raptorial, at least in large specimens.
Male, female. Black; knob of halter yellow; mid and hind tarsi sometimes
partly yellow from certain angles, but usually at least infuscated dorsally.
Frons chiefly gray microtomentose except for velvet black areas flanking
ocellar tubercle; interfrontal and fronto-orbital plates and frontal triangle
subshining and distinct; frontal triangle long, apex nearly midway on frons; cheek
narrow, 1/2 or barely over 1/2 breadth of 3rd antennal segment and 1/7 eye
height, with relatively broad polished subocular crescent 1/2 as broad as cheek,
anteriorly becoming a polished parafacial narrowly visible in profile; face deeply
concave in profile, vibrissal angle well produced anteriorly to a 45° angle, the
lateroventral corner of facial plate shining black and warped forward even beyond
the vibrissal angle, accentuating the angle; 3rd antennal segment small in both
sexes; palpus clavate, broad and flat in male (especially striking in large males),
but not as broad distally as in fig. 4.
Thoracic pleuron anterior to pleural suture entirely polished or virtually so,
including entire propleuron and area surrounding anterior spiracle, gray
microtomentose posterior to pleural suture, including entire pteropleuron. Male
with fore leg raptorial in appearance, fore coxa and fore femur elongate (similar
to fig. 22), especially evident in large specimens, the coxa over 3 times as long as
broad, and femur incrassate and |.3 times as long as other femora, with a row of
short, thick, even spines, and a postero-ventral row of similar but weaker spines;
fore coxa with numerous short but strong spines; in female fore coxa and fore
femur only slightly if at all elongate, without spines or spinelike bristles. Length,
2-3 mm (large males).
Sabrosky: Desmometopa of the World 61
Distribution: California, Arizona, Utah, Texas, Mexico.
Holotype male, allotype, and 23 paratypes (19 males, 4 females),
CALIFORNIA: San Bernardino Co., Verdemont, San Gabriel Mts., various dates,
including May 1, 1946 (holotype) and June 28, 1945 (allotype)(A.L.
Melander)[Washington]. |
Other paratypes [Washington except as noted]: CALIFORNIA [collector A.L.
Melander, except as noted]: 3 males, s. San Bernardino Co., Morongo Valley, Oct.
5, 1954; female, Palm Springs, May 6, 1946; 2 males, 1 female, sw. San Bernardino
Co., Upper Santa Ana River, June 18(male) and Sept. 2, 1950; male, Ortega
Highway, Mariana River, May 15, 1946; male, San Bernardino Mts., Mill Creek,
Aug. 17, 1952; male, San Diego Co., Yaqui Well, w. edge of Anza-Borrego State
Park, May 10, 1951; 8 males, 7 females, Los Angeles Co., San Dimas Canyon, Nov.
24, 1957, reared Dec. 16, 1957 - Jan. 3, 1958 (C.P. Christianson, J.P. Fonseca; ex
Opuntia), and 1 female, same locality, Feb. 2, 1958, reared Mar. 11 (R.E.
Ryckman) [Loma Linda]; 4 males, 3 females, Whittier, 1910, 1911 (P.H.
Timberlake). ARIZONA: 2 males, Superior, May 18, 1950 (A.L. Melander, "Datura
flower"); male, Globe, Oct. 13, 1948 (F.H. Parker); female, Yarnell Heights, I May
31, 1935 (P.W. Oman); male, female, Baboquivari Mts., Apr. 25, 1947 (A.L.
Melander); male, Yavapai Co., Cherry, Sept. 1968 (Judson May); male, Bowie, Dos
Cabezas Mts., Oct. 8, 1916 (E.G. Holt); female, Tucson, Nov. 15, 1936 (QO.
Bryant)[San Francisco]; female, Portal, Sept. 13, 1960 (H.F. Howden)[Ottawa];
female, Congress, Yavapai County, Apr. 23-26, 1967 (D.M. Wood)[Ottawa]; male,
Lower Bear Canyon, Tucson, Apr. 13-15, 1967 (D.M. Wood)[Ottawa]. UTAH:
male, Washington Co., Leeds Canyon, 1 mi. nw. Leeds, July 19, 1970 (G.F.
Knowlton et al.)[Logan]. TEXAS: 17 males, 14 females, Austin, Nov. 9-23, 1958
(Lynn Throckmorton)[Austin]; male, Austin, July 29, 1950; male, Austin, Oct. 27,
1901 (A... Melander); 4 males, 2 females, Big Bend National Park, various
localities, May 11-26, 1959 (J.F. McAlpine, W.R.M. Mason)[Ottawa]; 2 females, 10
mi.s. Charlotte, Sept. 13, 1955 (W.l.. Downes)[Lansing]; male, female, Brewster
Co., 25 mi. s. Marathon, Aug. 31, 1977 (Larry Bezark, “collected on Baccharis
glutinosa"). MEXICO: 2 males, Ciudad Victoria, Sept. 1965 (N.L.H. Krauss); 4
males, Morelos, Cuernavaca; March (2) and May 1945, and Apr. 1959 (Krauss);
male, Morelos, Hacienda Cocoyotla nr. Cuatlan del Rio, July 31, 1944 (Krauss);
female, Michoacan, Morelia, June 1965 (Krauss); male, Durango, Nombre de Dios,
Aug. 6, 1951 (P.D. Hurd, “Asclepias")[Berkeley]; 3 males, Durango, 11 mi. w.
Durango, June 20, 1964 (J.F. McAlpine)[Ottawa]; male, Hidalgo, Ixmiquilpan, 1700
ft., July 29, 1954 (J.G. Chillcott)[Ottawa]; 8 males, 1 female, Hidalgo, Pachuca,
1700 ft., July 29, 1954 (J.G. Chillcott)[Ottawa]; México, Atlacomulco, 8500 ft.,
Aug. 18, 1954 (J.G. Chillcott), and male, Teotihuacan, 6900 ft., Aug. 12, 1954
(Chillcott)[Ottawa]; 7 males, 2 females, Nayarit, Ahuacatlan, July 18-22, 1951
(P.D. Hurd, 4 males, 1 female "on fils. of Donnelsmithia Hintonli M &
C")[Berkeley]; male, Nayarit, 15 km n. of Chapalilla, Jive nd 9, 9, 1951 (P.D,
Hurd)[Berkeley]; 16 males, 1 female, San Luis Potosi, 10 mi. ne. San Luis Potosi,
Aug. 22, 1954 (R.R. Dreisbach) [East Lansing], and 3 males, 1 female, same
locality and date, (J.G. Chillcott)[Ottawa]; 2 males, | female, San luis Potosi, 5
mi. e. Ciudad del Maiz, Aug. 23, 1954 (Dreisbach) [East Lansing].
The raptorial fore legs of the male immediately suggest saquaro, but that
species has the dorsal stripe on the mesopleuron extending up to the anterior
spiracle, as in tarsalis, and other differences are noted under saquaro. It may be
noteworthy that both saquaro and melanderi were collected in San Dimas Canyon,
but the former in the spring and the latter in midwinter. The possible consistency
or significance of this apparent seasonal difference is not known.
62 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
The specific name is a noun in the genitive case, named in honor of my old
friend, the late A.L. Melander, ardent collector whose material will enrich
entomological studies for years to come.
51. Desmometopa aczeli, n. sp.
Predominantly polished pleuron; knob of halter yellow; all tarsi infuscated;
fore leg of male not raptorial.
Male, female. Black; halter knob yellow.
Frons heavily gray microtomentose except for velvet black spot on each side
of ocellar tubercle; interfrontal and fronto-orbital plates and frontal triangle
distinct because slightly shining; interfrontal plates narrow and short, posterior
ends at level of foremost upper orbital bristles; frontal triangle large, apex at
middle of frons and opposite posterior ends of the short interfrontal plates; cheek
moderately narrow, 1/2 breadth of 3rd antennal segment and 1/6 eye height, with
narrow polished subocular crescent that continues as a shining parafacial visible in
profile; face weakly concave in profile, vibrissal angle not produced, about 80°,
lateroventral corner of facial plate shining black but not strongly warped forward;
3rd antennal segment small in both sexes; palpus gently clavate, not enlarged in
male.
Thoracic pleuron virtually entirely polished black anterior to pleural suture,
the pteropleuron and posterior slope dull, microtomentose. Fore coxa and fore
femur not elongate, without spines, fore femur slightly incrassate but little longer
than other femora. Length, 1.75-2 mm.
Holotype male and paratype male, ARGENTINA: Mendoza, Vista Flores, Jan.
31, 1950 (M.L. Aczél); paratype male, Mendoza, Cacheuto, Feb. 5, 1953 (M.L.
Aczél)[Tucuman, paratype in Washington].
Even though the various characters lead this species to the final couplet with
melanderi, the two are not closely related. That species is large, with raptorial
fore legs, strongly produced vibrissal angle, and deeply concave face. In its
yellow mid and hind tarsi and the slightly microtomentose frons are distinctive.
The specific name is a noun in the genitive case, named in memory of Martin
Aczél, enthusiastic entomologist whose untimely death cut short a fruitful career
in Argentine entomology and the taxonomy of Diptera.
SPECIES OF "Desmometopa” NOW REFERRED ELSEWHERE
Agromyza albipennis Meigen 1830: Agromyza (Agromyzidae) (See separate
discussion after this list)
A. annulimana von Roser 1840: synonym of Leptometopa latipes (Meigen)
A. annulitarsis von Roser 1840: ditto
Madiza annulitarsis Zetterstedt 1848: ditto
Desmometopa anuda Curran 1936: Neophyllomyza
D. approximatonervis Lamb 1914: Neophyllomyza
D. fascifrons Becker 1907: synonym of Leptometopa niveipennis (Strobl)
Opomyza flavipes Meigen 1830: synonym of Phyllomyza securicornis Fallén
Madiza griseola Wulp 1871: synonym of Tethina illota Haliday (Tethinidae)
Agromyza latipes Meigen 1830: Leptometopa
Desmometopa luteola Coquillett 1902: synonym of Stomosis innominata (Williston)
Agromyza minutissima Wulp 1897: preoccupied name, renamed Desmometopa
wulpi Hendel, now in Neophyllomyza
Sabrosky: Desmometopa of the World 63
Siphonella niveipennis Strobl 1898: Leptometopa
Desmometopa simplicipes Becker 1907: synonym of Leptometopa niveipennis
(Strobl)
Desmometopa wulpi Hendel 1907: new name for Agromyza minutissima Wulp,
preoccupied: Neophyllomyza.
Agromyza albipennis Meigen
Agromyza albipennis Meigen, 1830, Syst. Beschr. 6: 171 (Europe).
A. albipennis; Becker, 1902, Ztschr. Hymenop. Dipt. 2: 339 [Two specimens in
Winthem Collection in Vienna and one in Paris found to belong to Agromyza].
A. albipennis; Hendel, 1931, Agromyzidae, in Lindner, F liegen Palaeark. Region,
Fam. 59: 98.
Desmometopa albipennis (Meigen) Séguy, 1934, Faune de France 28: 641
[Synonyms listed as D. tarsalis Loew of Becker 1907 and D. singaporensis
Kertlész].
A. albipennis Meigen, 1976, Abbildung der europaeischen zweiflugeligen
Insecten, nach der Natur, Pars III. Beitr. Ent. 26: pl. ccxvi, fig. 7.
The species has long been treated as a valid species in the family
Agromyzidae. However, Séguy (1934) referred it to Desmometopa “sec typ.”, with
tarsalis Loew (sensu Becker) and singaporensis Kertész as synonyms. The species
was said by Meigen to be in the Winthem collection, and that collection contains
two examples under the name albipennis, both Agromyza as noted by Becker
(1902) in his review of the Meigen types. Meigen's original description does not
apply to either of the species present in the syntype series of D. sinqaporensis
(q.v.) in such features as shining black-green body, white halteres, whitish wings,
and rather large black antennae, which are indeed features of Agromyza
albipennis. Further, the wing figured by Meigen himself (1976) is that of
Agromyza, not Desmometopa. I believe, therefore, that the Winthem specimens
must be regarded as the original syntypes, hence in Agromyza, and that the Paris
specimen was a later and erroneous addition, and misidentified. Incidentally, it is
actually D. m-nigrum (Zett.) and not D. singaporensis!
64 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
LITERATURE CITED
(other than references in synonymies)
Becker, Th. 1902. Die Meigen'schen Typen der sogen. Muscidae acalypterae
(Muscaria holometopa) in Paris und Wien. Ztschr. Hymenop. Dipt. 2: 209-256,
289-320, 337-355.
1907. Desmometopa. Wien. Entomol. Ztg. 26: 1-5.
Bezzi, M. 1928. Diptera Brachycera and Athericera of the Fiji Islands.
British Museum (Nat. Hist.), pp. vill + 220.
Bohart, G.E., and J.L. Gressitt. 1951. Filth-inhabiting flies of Guam.
Bernice P. Bishop Mus. Bull. 204: vii + 152.
Curran, C.H. 1934. The families and genera of North American Diptera.
512 pp., New York.
Duda, O. Beitrag zur Kenntnis der Palaarktischen Madizinae (Dipt.).
Natuurhist. Maandblad 24: 14-16, 24-26, 37-40.
Grensted, L.W. 1956. On the gender of the generic names Desmometopa and
Leptometopa (Dipt., Milichiidae). Entomol. Monthly Mag. 92: 405.
Gressitt, J.L. 1956. Desmometopa tarsalis Loew [Note]. Proc. Hawaiian
Entomol. Soc. 16(1): 4.
Griffiths, G.C.D. 1972. The phylogenetic classification of Diptera
Cyclorrhapha with special reference to the structure of the male postabdomen.
Series Entomologica (Dr. W. Junk N.V.) 8: 341 pp.
Hardy, D.E., and M.D. Delfinado. 1980. Insects of Hawaii, 13 (Diptera:
Cyclorrhapha III): 451 pp.
Hennig, W. 1937. Milichiidae et Carnidae. (Fam.) 60a: 91 pp., in Lindner,
Die Fliegen der Palaearktischen Region, Lfg. 115.
_ _.. —«(1939. Beitrage zur Kenntnis des Kopulationsapparates und der
Systematik der Acalyptraten. II. Tethinidae, Milichiidae, Anthomyzidae und
Opomyzidae. (Diptera). Arb. Morphol. Taxon. Entomol. Berlin-Dahlem 6: 81-94.
_. 1941, Verzeichnis der Dipteren von Formosa. Entomol. Beih.
Berlin-Dahlem 8: iv + 239.
| Illingworth, J.F. 1926. Desmometopa m-nigrum (Zett.)[Note]. Proc.
Hawaiian Entomol. Soc. 6(2): 224.
__. 1929. Desmometopa tarsalis Loew [Note]. Proc. Hawaiian Entomol.
Soc. 7(2): 233-4.
International Commission on Zoological Nomenclature. 1958. Declaration
39: Review under Copenhagen Decision 85 of the Rules relating to the gender to
be attributed to certain classes of generic names...Opin. Declar. Internat.
Commn. Zool. Nomen. 19(4): i-xviii.
ee : a 1961, 1964. International Code of
Zoological Nomenclature, pp. xviii + 176. (2nd Edition, 1964, pp. xx + 176).
Johnson, C.W. 1913. Insects of Florida. I. Diptera. Bull. Amer. Mus. Nat.
Hist. 32: 37-90.
Kato, M., and Katsushige Hori. 1952. Studies on the associative ecology of
insects. VI. Larval association of flies during the summer in Sendai and its
vicinity, Japan. Tokyo Univ. Sci. Rpts., ser. 4 (Biol.), 19: 238-246.
Knab, F. 1915. Commensalism in Desmometopa (Diptera, Agromyzidae).
Proc. Entomol. Soc. Wash. 17: 117-121.
Konow, F.W. 1907. [Footnote to review of Becker 1907 on Desmometopa].
Ztschr. Hymenop. Dipt. 7: 355.
Malloch, J.R. 1914. Formosan Agromyzidae. Ann. Mus. Nat. Hungarici 12:
306-336, pls. 9-10.
_. 1924. Notes on Australian Diptera. No. iii. Proc. Linn. Soc. N.S.
Wales 49: 329-338.
Sabrosky: Desmometopa of the World 65
__ 1927. Notes on Australian Diptera. No. x. Proc. Linn. Soc. N.S.
Wales 52: 1-16.
1934a (June 23). Insects of Samoa, Part VI. Diptera, Fasc. 8: 267-328
[British Mus. (Nat. Hist.)].
1934b (Nov. 24). Acalyptrata (concluded). pp. 393-489, pl. 8,
text- -figs. 69-84, in Diptera of Patagonia and South Chile, Part VI, fasc. 5 [British
Mus. (Nat. Hist.)].
McMillan, R.P. 1975. Observations on flies of the family Milichiidae
cleaning Araneus and Nephila spiders. Western Australian Naturalist 13: 96.
Meigen, J.W. (ed., G. Morge). 1976. Dipteren-Farbtafeln nach dem bisher
nicht verdffentlichten Original-Handzeichnungen Meigens. Pars III: Farbtafeln
CLXI-CCCV. Beitr. Entomol. 26(2): colored plates as noted.
Melander, A.L. 1913. A synopsis of the dipterous families Agromyzinae,
Milichiinae, Ochthiphilinae and Geomyzinae. Jour. N.Y. Entomol. Soc. 21:
219-273, 283-300, pl. 8.
Mulla, M.S., and M.M. Barnes. 1957. On laboratory colonization of the eye
gnat, Hippelates collusor Townsend. Jour. Econ. Entomol. 50: 813-816.
| Nikitin, M.I. 1965. Insects from boxthorn berries and other non-commercial
fruits in New South Wales. Australian Jour. Sci. 27: 264-267.
Peyerimhoff, P. de. 1917. Phorésie et commensalisme chez les
Desmometopa. Bull. Soc. Entomol. France 1917: 215-218.
Rabaud, E. 1924. Le commensalisme de Desmometopa sordida Fall. La
Feuille des Naturalistes 45(n.s.): 18-19.
Richards, O.W. 1953. [On commensalism of Desmometopa with predacious
insects and spiders]. Proc. Roy. Entomol. Soc. London, Ser. C., 18: 55-56.
Ryckman, R.E., and C.T. Ames. 1953. Insects reared from cacti in Arizona.
Pan-Pacific Entomol. 29: 163-4.
Sabrosky, C.W. 1965a (Feb. 1). East African Milichiidae and Chloropidae
(Diptera). Stuttg. Beitr. Naturk. 138: 1-8.
1965b (Aug. 23). Family Milichiidae. pp. 728-733, in Stone et al., A
catalog of the Diptera of America North of Mexico. Agric. Handbook 276: iv +
1696. ,
1973. 75. Family Milichiidae, pp. 1-12, in A catalogue of the Diptera
of the Americas south of the United States (Museu de Zool., Sao Paulo, Brazil).
1977. Family Milichiidae. pp. 270-274, in Delfinado and Hardy, A
catalog of the Diptera of the Oriental Region (University Press of Hawaii,
Honolulu).
1980. 75. Family Milichiidae. pp. 686-689, in Crosskey, Catalogue
of the Diptera of the Afrotropical Region (British Museum, Nat. Hist., London).
Séguy, E. 1934. Dipteres (Brachycéres)(Muscidae Acalypterae et
Scatophagidae). Faune de France 28: 832 pp.
Nae 1938. Diptera L. Nematocera et Brachycera. pp. 319-380, in Jeannel
(ed.), , Mission Scientifique de l’'Omo, Tome IV (Zoologie).
Swezey, O.H. 1952. Insects from decaying blossoms. Proc. Hawaiian
Entomol. Soc. 14(3): 357.
66 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Desmometopa: Dorsal aspect of head, (1) varipalpis, (2) singaporensis; (4) palpus of
gressitti; lateral aspect of head, (3) varipalpis male, (5) singaporensis male, (6)
Sabrosky: Desmometopa of the World 67
Desmometopa: Dorsal aspect of head, (10) interfrontalis; lateral aspect of head,
(9) interfrontalis, (11) ciliata, (12) atypica, (13) postorbitalis male, (14) inaurata,
(15) pleuralis, (16) microps female, (17) microps male.
68 Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
Desmometopa: Lateral aspect of head, (18) tarsalis, (20) lucidifrons; (19) hind
tibia, leptometopoides male; (21) antenna, magqnicornis male; (22) fore leg,
saquaro; left thoracic pleuron, semi-diagrammatic, (23) m-nigrum, (24) ciliata,
(25) varipalpis, (26) tarsalis, (27) glaucanota, (28) latigena.
Contrib. Amer. Ent. Inst., vol. 19, no. 8, 1983
aczeli, 20, 62
albipennis, 62, 63
aldabrae, 19, 53
annulimana, 62
annulitarsis v. Ros., 62
annulitarsis Zett., 62
anuda, 62. .
approximatonervis, 62
argentinica, 20, 59
atra, 4/
atypica, 17, 39
blantoni, 17, 35
ciliata, 18, 39
-~Desmetopa, 13°
Desmometopa, 2, 13
Desmometopa (sg.), 3
evanescens, 16, 28
fascifrons, 62
flavicoxa, 16, 30
flavipalpis, 19, 49
flavipes, 62
floridensis, 16, 33
glaucanota, 16, 32
gressitti, 19, 21, 54
griseola, 62
halteralis, 62
inaurata, 14, 22
indistincta, 17, 21, 34
interfrontalis, 15, 28
kandyensis, 19, 54
latigena, 15, 24
latipes, 62
leptometopoides, 18, 20, 40
Liodesma, 13
Liodesmometopa, 13
lucidifrons, 14, 23
luteola, 62
magnicornis, 19, 21, 51
melanderi, 20, 21, 60
meridionalis, 17, 21, 34
(Invalid names underlined)
microps, 15, 21,25
minutissima, 62
m-atrum, 47
m. nigra, 27
m-nigrum, 15, 27
nearctica, 20, 58
nigeriae, 14, 21
nigrohalteralis, 16, 31
niloticum, 27
niveipennis, 63
nudigena, 19, 21, 48
obscurifrons, 17, 37
palpalis, 44
parafacialis, 17, 21, 38
philippinensis, 19, 21, 52
Platophrymyia, 2, 3, 13
pleuralis, 14, 21
postorbitalis, 15, 21, 26
propeciliata, 19, 51
saguaro, 20, 21, 55
semiaurata, 22
simplicipes, 63
singaporensis, 18, 20, 44
sordida, 18, 47
srilankae, 19, 50
stilbopleura, 20, 59
tarsalis, 20, 56
terminalis, 17, 36
tristicula, 44
varipalpis, 18, 20, 41
woldai, 16, 29
wulpi, 63
60,4, 15, 25
sn. 1, 16, 29
sp. J, 16, 31
SO. A, 16) 24, 32
sp. l, 19, 48
sp. M, 19, 52
sp. N, 19, 53
spo, O, 20, 39
69
ae
ee
a ah i
aah i ; 7 ee
tien
Hi
ue Eiger: 25
eget
FS
An
eS
, Sous
PL oe SEP ee peet Ye
$< *
ae
Deneve
a
ee
nee aly. Gow:
Pe me tos
eae #s a= de ae
Se See
Pi FS
reer code oe oe
PA:
a v; }
wore om.
SPY Lge pot
es Pe
pe eae oe 4
F
> 4 > aa iD i
ae reas s
eg See eee pe Be
enw t:
peas
nae
A? ay
a oF PES LS
Foxe 2% eee as
pee ak
am
Sg bes ih a ol
iw be ih
oy eS one a
Ses
aS i Sah ed ha 4
ao. See Noes ARE
PEW: #: * as ei pores ie va vebs Be
vi bh we ‘ §
i ee Sd
Pon veges ae
Sed
obs Ie
a Hogs Pe Be
<8 5
ey
ate, atte
ro See ys
BLE VS St SP EEE EE DEAD e PEs
: See ne LSP at se ice pis ANA GD Ds bye
“> A AS Pee PHF eee oe ay
Cees
aos a 4 .
49 oe ~
“a ePe pape ety
ee eee ee ge S
PP OE te ENS ee END
PRAT OS ah ee,
eae: Sy 2 7 eg
TSh4)
PAPERS Og a SOW:
‘ Sree yy Dis
7 ae Pane ee reps aes
OS te iar et uae ana
ey a
EN eny: pe!
ieee as
2
PDE oe
yh AN .
eeeeestars An
iS Soeate
2 sPyates> ah
Be :
: Sao wate a PA
sa Se ae a od
07 SP eae Saat
ISIAH
re
Yo Regs a oe Pe pe
» 3a 252 Pe 2
irae} avy
er Corer e ness ¥ :
BD od st aoe ie PRIS
pid chy 4
PES Se oe ge Sob ae aS We ated 4
dee Anh ase dey WG, oes
SP NN Fe
J ee a 5. -
i
ae gore EEE PE RIE G S :
wi Sch NP eae Sd SS re Se RH
% rh he kg be SEL Bs
ee rk eee SS
F ia as = Se ES
Boe oth
SEE NS
ae
S36 =o a! NE AS ee ee
v2 tet >
ATA a ae
wee are
we
oe wee See
of a AS Ge wD B
Pe ee ee G
PME NTS De |
pare eS
;
a a
SM Pe oe
At = Veet Pa ea a pa
eo poh
worm
_
sees
bat ee mas
veri eae. hs ee eA ve
wes
PEP See OL ee ey
eet tal ee
. 24 pepebree
e a Soy wena.
oh ees $y
Pe
ae:
ae ae epee
ghee die
reese, * aie
Veeres LW dee ce 2: ane
Se Re eae
cers ak
fe
DS Ane or ee 2 e ee
St SP Ag yay sheesh Ses ae
She
ENGR 5h Sg es ha
aren ny ee
i GE SA Paw
PERSO OS Serer wow & 8 peeps
é Hosier wh
Sate
Sv ee ee
Ch Atte Ser ae
TAG ees sak
=e
Pie FSP
r as
Sore miee peegeee n
;
ee
EAH Po Wie He
ere oe we ay nan v
beds bs. oT
he SELES eet
gente 5 uly
me
bs
SNE tm
>:
Seat oa A Ara RA
dh eS
ews
ey ae Sey:
= Pee Pee
wey aaron
we
‘ Pe wie be oes ye
Ee Se ae
PAK DS A AD SRA CR 3p EP SO
Wek dh kitad’ Od Se ce
Tee MANES : 5
PM oe
Fee at
a ke +3
2x, peice LAE aR Oe
Bie eee ee Reeser Se se SAC te F
he f
Wh Pedy adhe Ph aby 2 ear hy
SRS is a)
: cee a
: pA
to ee a *
ab a oh aed 44 ia Winn
were Pe PEP PSP Re
: Poa eae ore gh ae OP ta eee ate acat
Lp AEA eae COSC A ER eG a
a teh Lend Vor aes pf tae od
os ee Rae mo re s yey 4
eye pe don a a we :
ae eee peek Pe eS PS hie eae a Py
* ‘Gee Ds we Fee ay es ee
3 » LEAKS west on! 4
. Pe A Ee Ra &
Poe oy Peer?
EE wena 4 ad La as
ee wey
de he aS ee pe
Std eo
¥
ee BY wyeercey a
Wats Pawns Sahar
ead
SP at gh AP et re ee
oe es UP vee ee Ges
gh Peers
aN ede oe: aa nl het
LBRO LH | ‘
Pe ate oer dy Re Re Ps
Pre oe
se os See od
anna we :
eeu. SPewe Seow eee
rey geen gs Pet ies SP Set
Sb ks ees
Rua hie ee o a
dows a Payee? 5
720 eo age
ee Se a
poe rood ez
=
> ite
eres aygest
swe on os ¥
pos ee *
oe Bees
Shane ee
hd pepe “e rit. Pepeosee:
sree sted ryonee es os pad iiss
ab Sarees Bethe
sees aes rane: + 2
Aan
Sefoty
Sen
Ess PBS
ete ge
FSS A
=a
Syrices rk Hee
poietge + ad es e - rs See
peeree we ote
ae Seely pierisigs ee. ea
Eat Det acs) en
rece: 4
ReEosy et er Pee A Se a we
. y
Pere re. hod
Sere ses [Shak
NP wed Soa w:
Lore oes | A dk
AE END Ge a
ee Sesh ore rie yes
< bd
®
b ws we SA A ah
eae YR eryee yee ee eetoy wee we Pee) ee
ee at See vee Soe wees see 7 Preece ee
Gesoig ewe 5 em
Fe 3 aa
bape pds - Ee ie Sete i 54S 3
eae eevee: Se Pee yy Pi
padres idee ah Se SED &
Sache eRe Pee ney ee
UF ee
5.3 sieeet
4 - ial
SP Hops ry + d
ae Land
PE we PY eas 7
be >
erase “ate 4 2
‘i C desagt ds 2 ‘
eee o 2 Sen ey z i Ras se
pene ee *
Eas fee *
: ah se
eetets ee ee ae
Los
th
eS
{ard
VigVgy
apes
ee: oe iow 2 Uy
ow
BP Ve ed
‘ ; vere, ee ee “ae yore
4
bal
Vewed
et eee
Poet
Pavey
ea eee
. ¢