Vol. XXX JANUARY, 1954 No. 1
THE
PAN-PACIFIC ENTOMOLOGIST
CONTENTS
USINGER—Howard Madison Parshley.........-.-...----.-..-ceccsscsssencessnenesncenseennaes 1
GRESSITT, FLANDERS, & BARTLETT—Parasites of citricola scale
in Japan, and their introduction into California... wu... .eseeeeeeeeeee- 5
BROWN—tThe synonymy of the ant Aphaenogaster lepida Wheelet........ 10
LINSLEY & MacSWAIN—Observations on the habits and prey of
Bucercerisruticeps “Sculle nes 2 a5 soe asco acs. Secs arl aad tact Ms eB oes ce 11
DAY—New species and notes on California mayflies Wow... eee 15
DAY—New species of California mayflies in the genus Baetis................ 29
MALKIN—A new northwestern melandryid.....2...2...2.---ssece-1eeeeeeeseneeeeeeeeee 35
MICHENER—Descriptions and records of North American Hoplitis
ANG eATUNOCO PA mus eter rs ake ek ee As rs nae Ny ee Met eis, Se 37
ESSIG—Change of the species name of Myzus langei Essig to Myzus
Callaniger TiSsl go O92 ess Sete once ene ee oats etcotene ce Shnika Ua ree TLS Be 52
PHILIP—New North American Tabanidae (Diptera). Part IV. Zophina
new genus for “Apatolestes” eiseni Townsend from Lower California 53
WALL—Mirolepisma deserticola silvestri, a myrmecophile from
California
WIRTH—A new intertidal fly from California, with notes on the genus
Nocticanace “Malloch; .wteset.cncap stars .o eer ces Riek tee
MICHENER—Observations on the pupae of bees. ...u...........ssceceeceeseceeeeseee 63
MADDUX—A new species of Dobsonfly from California... 70
WALL—A re-described species and a new genus and species of the family
Eepismatiade lit) Calitopran ess. the. tac s tats, praeunentetaviere ea neaeaseresons nee
Book nGticessand tevyiew sterner tA... ek ance eee SAN esduneles cae 10, 14, 34
Proceedings—Pacific Coast Entomological Society_... 2.2.2 e-..e.seceeeeneeeeeeeee Te!
SAN FRANCISCO, CALIFORNIA ¢ 1954
Published by the PACIFIC COAST ENTOMOLOGICAL SOCIETY
in cooperation with THE CALIFORNIA ACADEMY OF SCIENCES
THE PAN-PACIFIC ENTOMOLOGIST
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BULLETIN OF THE CALIFORNIA INSECT SURVEY
1:1 Middlekauff, W. W. The Horse Flies and Deer Flies of California
Ug cg ere Rego fee hate 1g 025] | ER aca Penns Menon eg Oo oP $0.35
1:2 Freeborn, S. B., and R. M. Bohart. The Mosquitoes of California
jag meee hs eas meso Beal [iv ta cao a Es jl [aa ce a Pe nn ene ae $0.50
1:
w
Linsley, E. G., and J. W. MacSwain. The Rhipiphoridae of Cali-
fornia (Coleoptera). Pp. 79-88, pl. 9. June 29, 1951.............-..---.---- $0.25
1:4 Hurd, P. D. Jr. The California Velvet Ants of the Genus Dasymutilla
Ashmead (Hymenopéera:Mutillidae). Pp. 89-118, pl. 10. August
BRR A. ho lorarte cere Re Ascen SN Ris ht te ORE nee ae a ee oh tha gl pe $0.35
1:5 Hurd, P. D. Jr., and E. G. Linsley. The Melectine Bees of Cali-
fornia (Hymenoptera:Anthophoridae). Pp. 119-140, pl. 11, 5 maps.
TT gist 1S 5 Ween Aa iM Ad che AAT MORE DROS, Ra ee SER PS wot $0.25
1:6 Hurd, P. D. Jr. The Scoliidae of California(Hymenoptera:Aculeaia).
Pp. 141-152, ple: 12 and. 1S. Jume 27, Y95 2. co. ceckatecese cde econ $0.25
2:1 Keifer, H. H. The Eriophyid mites of California (Acarina:Erio-
phyidae). Pp. 1-128, pls. 1-39. December 12, 1952... $2.00
2:2 Pritchard, A. Earl The Gall midges of California (Diptera:
Ttonididae olim Cecidoryiidae). Pp. 125-150, pl. 40. February
MALS RIAs Tee oa eel Wiad: A. Wise) ona. MOO | Want SP - ae Me Rated Rea, BA £0.35
Send orders to: UNIVERSITY OF CALIFORNIA Press, BenKELEY 4
Entered as second class matter, February 10, 1925, at the post office at
San Francisco, under act of August 24, 1912.
The Pan-Pacific Entomologist
Vol. XXX January, 1954 No. 1
HOWARD MADISON PARSHLEY
1884—1953
Rosert L. UsincER
University of California, Berkeley
The passing of Howard Madison Parshley on May 19, 1953,
brought to a close the earthly career of one of the most versatile
hemipterists of our time. Born in Hallowell, Maine, on August 7,
1884,:Dr. Parshley spent his early teens on a farm in eastern New
York State. “This experience,” to quote from a biographical sketch
by Dr. Alexander Leslie in the Smith College Memorial Service,
“cave him insight into country life, and, with the help of a tattered
Cornell leaflet on insect collecting, probably determined the direc-
tion of his major professional interests.
“Dr. Parshley attended the Boston Latin School from 1901 to
1905. He then went to Harvard University from which he was
graduated in 1909. During the period of 1906 through 1909, he
also attended the New England Conservatory of Music. In 1910,
he took his master’s degree from Harvard. At this time he was
married to Nancy Fredricson. They went to the University of Maine
where for three years he was instructor in biology, the exact posi-
tion which his daughter, Elsa, was to fill some years later. In 1914
he returned to Harvard, where he was awarded his Doctor of
Science degree in 1917. That same year he received an appointment
in the zoology department of Smith College, where he was to
complete his life’s work.”
It would be quite impossible and out-of-place to try to cover
the whole of Dr. Parshley’s varied career in this brief article. His
published articles and reviews alone exceed 400. He was an accom-
plished musician, playing at the first stand in the bass section of
the Springfield Symphony Orchestra for many years. Additional
interests included poetry, radio technology, sports and gardening,
but his music was particularly close to his heart, and provided a
fitting climax to his career only a week before his death. May 13th
was Northampton’s first “Symphony Day” when the Springfield
Symphony came to town to play for 2,000 school children in the
afternoon and for the community as a whole in the evening. He
demonstrated the double bass for the children in a way which
2 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
brought the house down. He was first bass for these concerts and
was especially interested in the event as his daughter was chairman
of the whole affair.
_ At the time of his death, Dr. Parshley had completed arrange-
ments for the disposition of his insect collection and entomological
library. The collection of 23,980 specimens was sold to the Cali-
fornia Academy of Sciences, to take its place beside that of his
colleague of former years, E. P. VanDuzee. It is interesting to note
that the collection contains specimens taken as recently as 1947,
JANUARY, 1954] USINGER—PARSHLEY OBITUARY 3
long after his last publication on insects. The collection alone would
be an impressive monument to a life’s work, including, as it does,
numerous type specimens, beautifully prepared specimens of .
typical European species and the definitive collection of Geocorinae
of the world which was purchased from A. L. Montandon in 1920.
But Dr. Parshley’s entomological contributions were far greater
than this. In the brief span of years from 1914 to 1925, fifty-three
papers were published, dealing principally with the Aradidae,
Tingidae, Miridae, Gerridae, Veliidae, Nabidae, Lygaeidae and
Anthocoridae. His greatest taxonomic work was the “Essay on the
American Species of Aradus,” published in 1921. This is still the
definitive work on this subject and could well serve as a model in
style and thoroughness of treatment for future students in this
and other groups.
Without doubt, his greatest service to hemipterology was his
“Bibliography of the North American Hemiptera—Heteroptera,”
(1925) a carefully prepared and beautifully printed fiftieth anni-
versary publication of Smith College. His interest in the bibli-
ography of the Hemiptera led to his appointment as managing
editor of the General Catalogue of the Hemiptera. This project was
organized by a group of hemipterists at the Cincinnati (1923)
meeting of the American Association for the Advancement of
Science. The Catalogue was published by Smith College, five fas-
cicles having appeared in 12 parts (2,177 pp.) between 1929 and
1949. It is certainly not accidental that this Catalogue, under Dr.
Parshley’s guidance, stands as the most ‘complete (for the com-
paratively small number of families dealt with) and faultlessly
prepared catalogue of any group of insects to date.
Dr. Parshley’s publications on the Hemiptera were not numer-
ous, and covered only a brief decade ending over a quarter of a
century ago, his travels were not extensive, and his personal con-
tacts with fellow hemipterists were few. How then does it happen
that his influence was so great? The answer lies in his scholarly
approach and his penetrating mind. It is evident from his publica-
tions that Dr. Parshley understood the fundamentals of biology.
Therefore his judgment was good in matters of classification,
nomenclature and distribution. That he also understood human
nature and the basic essentials of human life is evidenced by his
extensive writings, particularly since 1925, in the social sciences.
nS
THE PAN-PACIFIC ENTOMOLOGIST VOL. Xxx, NO. 1
There is no need to repeat the list of enomological publications
given by Dr. Parshley himself in the “Bibliography” (1925), but a
few quotes from his writings on Hemiptera will serve to illustrate
Dr. Parshley’s philosophy and at the same time may provide the
general entomologist, who might otherwise overlook these buried
treasures, with food for thought. Dr. Parshley—“On the Prepara-
tion of Hemiptera for the Cabinet’ (1919) —deplores the “practical
spirit which eliminates the study of the classics, elevates every
trifling trade to the dignity of an academic pursuit, and in general
places the things of the dollar above the things of the spirit. The
science of entomology has reached its present state of advancement
very largely through the unpaid effort, the labor of love, of enthu-
siasts, and we may hardly look for any progress that is worthwhile,
in the technique of mounting specimens or in matters of higher
import, if entomologists, professional or otherwise, come to be
actuated as a class by any spirit other than that of the true
amateur.”
Dr. Parshley’s keen mind saw through the superficialities of
some of the work of his contemporaries and led him into a con-
troversy which, both in correspondence and in spirit, was devas-
tatingly logical, stimulating, and at all times, dignified. His views
on subspecific variation, expressed 30 years ago, were well ahead
of their time and his remarks on “criticism” in a biographical
article on “Ernst Evald Bergroth: Master Hemipterist (1857—
1925)”’ are perhaps more pertinent today than at the time they
were written. “It is... in this... field... of fiery and often
magnificently destructive criticism, that Bergroth did some of his
most important work. The sanative influence he exerted and will
continue to exert upon beginning students—through his attacks on
ignorant and careless workers, and his lively appreciation of
thorough and honest effort—will prove to be not the least valuable
element in his enduring contribution. No student can afford to
neglect the study of Bergroth’s masterpieces in the art of con-
troversy; for when mutual criticism fails, science loses one of its
most essential means of progress.”
In his article “On the Life of William T. Davis,” Dr. Parshley
stated his concept of the problem of living, a problem which, in
retrospect, it would appear that he solved so successfully. “He
(referring to Davis) solved in his fashion the problem all must
face: how at once to follow the inner light, meet the material de-
mands of life, and maintain a genial warmth in human relations.”
JANUARY, 1954] GRESSITT, ET AL—CITRICOLA SCALE 5
PARASITES OF CITRICOLA SCALE IN JAPAN, AND
THEIR INTRODUCTION INTO CALIFORNIA*
J. LinsLey Gressitt,? STANLEY E. FLANDERS,*®
AND Buatr Bartuett* ®
University of California Citrus Experiment Station,
Riverside, California
Citricola scale in California, described by Campbell in 1914 as
Coccus citricola, was subsequently shown to be the same species
as that from Japan, described by Kuwana earlier in the same year
as Lecanium pseudomagnoliarum. Rules of scientific nomenclature
require the use of the species designation first applied; hence, the
adoption of the name Coccus pseudomagnoliarum (Kuwana), and
the retention of the term citricola for the common name of this
scale.
The citricola scale is a major pest of citrus in central California,
and infestations sporadically become severe in many of the inland
citrus areas, from Butte County in the north to the Imperial Valley
in the south. Because of the general restriction of economic in-
festations of citricola scale to areas of extremely high summer
temperatures and low humidities, and its foreign origin, the oc-
currence of this scale in the climatically dissimilar area of Japan
appears as an anomaly. Accumulative evidence that citricola scale
is not indigenous to Japan has been supported, also, by other
biological evidence relative to its host preferences and parasitic
fauna. Its recently reported occurrence at subeconomic levels on
citrus in Iran (Kaussari, 1946) further supports the belief that
it may be native to the drier areas of Asia, and that it found its
way to California by a circuitous route, through Japan.
1 Paper No. 770, University of California Citrus Experiment Station, Riverside,
California.
2 Temporarily employed, 1947-1951, by the University of California for investi-
gation of natural enemies of citrus insects in Asia. Now with the B. P. Bishop
Museum, Honolulu, T.H.
3 Professor of Biological Control and Entomologist in the Experiment Station.
4 Assistant Entomologist in the Experiment Station.
5 The authors acknowledge their indebtedness to their colleague, Harold Compere,
who identified all the parasites mentioned in this paper.
6 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
Records of the Department of Biological Control of the Uni-
versity of California on the occurrence of natural enemies of
citricola scale in Japan begin with the year 1922. At that time,
C. P. Clausen, while exploring the Far East for the Federal Gov-
ernment in connection with another problem, sent to California
shipments of citricola scale which yielded the parasites Coccopha-
gus yoshidae Nakayama, Coccophagus japonicus Compere, Ani-
cetus annulatus Howard, and Metaphycus orientalis Compere
(Compere, 1924.). None of these species was received in condition
for establishment in California at that time. Subsequent records
-(Compere, 1926; Flanders, 1942) indicated that Aneristus cero-
plastae Howard and Microterys okitsuensis Compere were possible
citricola parasites. The attack upon citricola scale in California
by the imported parasite species Coccophagus caridei (Bréthes),
Metaphycus stanleyi Compere, and Metaphycus helvolus (Com-
pere), aiding in the work of the previously established Metaphycus
luteolus (Timberlake) and Coccophagus lycimnia (Walker), has
been reported by Flanders (1942).
In 1951 an opportunity was afforded the senior author to com-
plete the introduction of citricola parasites from Japan, as well
as to survey the area for other possible beneficial insects for use
against pests of California agriculture. After obtaining his release
from internment by Chinese on the Asiatic mainland, where he
had been employed in a search for red scale parasites, he spent
the period from February through June, 1951, in Japan, in a search
for citricola parasites. The area from northernmost Honshu to
southernmost Kyushu was covered in the search.
In this brief exploration, citricola scale was found to be
relatively rare in Japan. It was taken from cultivated citrus in
orly a few isolated plantings, the trifoliate orange, Poncirus tri-
foliata, serving as primary host for the species. On this commonly
used Japanese hedge plant, citricola scale was found to be spo-
radically distributed throughout the warmer half of Japan and
somewhat more generally distributed in the cooler northern and
central mountainous parts of the country.
In Japan, as in California, citricola scale has only one well-
defined generation a year. This even-broodness is of considerable
interest, in view of the fact that on potted citrus in outdoor cloth
cages at Riverside this scale exhibits an uneven double-brooded-
JANUARY, 1954] GRESSITT, ET AL—CITRICOLA SCALE ch
ness. Even-broodedness under natural conditions represents a
distinctly disadvantageous condition for the successful operation
of parasitic species, since it is not conducive to their perpetuation
during periods when host size is unsuitable. Under such conditions,
a complement of alternate hosts is generally required, unless un-
usual modifications in the life history of the host or its parasites
occur. In Japan the possible alternate hosts of the lecaniine group
were varied and abundant, a fact that made ready recognition of
certain parasitized stages of citricola difficult. It was often im-
possible to determine whether parasitized individual scales were
the species sought or a closely related species.
In Japan there is a somewhat greater disparity in the develop-
mental stages of citricola scales of the warmer and colder areas
than commonly occurs in California. There was approximately two
months’ difference between the beginning of spring scale growth
in northern and southern Japan. This inequality of growth served
to extend the range of scale development that could be surveyed
for parasites during the period of explorations. It fortunately per-
mitted the search for parasites to cover a portion of that period
when the scale is in a characteristically colored hibernating or
nongrowth period. Since none of the known parasites of citricola
attack this stage, and since it offers the greatest possibilities for
continued parasite reproduction, emphasis on exploration of this
scale stage was most desirable.
Citricola scale is believed to be under effective biological con-
trol in Japan. The densest populations discovered were observed
as they decreased in abundance and as parasitization approached
100 per cent. It is believed that in isolated localities the scale
population may be nearly exterminated by the action of parasites,
and that two or more years may be required for attainment of
another peak population density. This effectiveness of parasitiza-
tion is probably correlated with the existence of an abundance of
closely related alternate host scales which serve to perpetuate the
parasites over unfavorable citricola stages. Such reasoning is fur-
ther substantiated by laboratory tests on the imported parasites at
Riverside, which indicate wide range in host species.
Sixty-one shipments of parasitized citricola scale were received
at Riverside from Japan. These were processed through quaran-
tine, and secondary parasites of the genera Cerapterocerus, Tetra-
stichus, Cheiloneurus, and Thysanus were eliminated.
8 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
The following five chalcidoid species, all known as citricola
parasites, were obtained: Coccophagus japonicus Compere, Coc-
cophagus yoshidae Nakayama, Coccophagus hawaiiensis Timber-
lake, Microterys okitswensis Compere, and Anicetus annulatus
Howard. In addition, Microterys flavus (Howard), Metaphycus sp.,
Aneristus ceroplastae Howard, Blastothrix ozukiensis Ishii, Coc-
cophagus ishiit Compere, and an unrecognized yellow Coccophagus
were taken from indeterminate host material. Some of the last-
named species are still being tested for possible use against other
lecaniine scale pests in California. No effective predators of citri-
cola scale were found in Japan. Chilocorus tristis Faldermann ap-
peared as an incidental predator, much as do the few ladybird
species sometimes observed in California.
The five primary citricola scale parasites from Japan were
responsive to culture on soft (brown) scale in the insectary. This
greatly simplified production for citricola liberation. All five
species were easily distinguishable by their effects on the appear-
ance of the host. Coccophagus japonicus attacks scales 1.0-2.0 mm.
in length and colors the derm on the dorsum of the scale jet black.
C. hawatiensis attacks scales 1.6—2.5 mm. in length and imparts
only a slight brownish tinge to the scale derm after emergence.
Anicetus annulatus attacks scales 1.3—2.4 mm. in length and par-
tially blackens the derm on the dorsum of the scale. C’. yoshidae
attacks scales 1.7—3.0 mm. in length and turns the scale derm dark
brown. Microterys okitswensis, the only one of the five that is
gregarious, attacks scales 1.5 mm. in length as a solitary parasite,
whereas 3 or 4 parasites may attack and emerge from a larger
single scale, leaving it in a honeycombed-cocoon condition. The
meconia of the five species also present differences which are
useful in distinguishing the work of the various species.
Reproduction and liberation of the five primary parasites of
citricola scale have been completed. Their release against other
lecaniine hosts remains to be tried. Over 25,000 females of Coc-
cophagus japonicus, 2,000 of Microterys okitsuensis, 20,000 of C.
hawaiiensis, 3,000 of Anicetus annulatus, and 3,000 of C. yoshidae
have been liberated, primarily in the central California area. The
first three species have been recovered from places of liberation.
The best prospects for effective control are offered by the species
C. japonicus, providing this species can bridge the stage of scale
unsuitability. Its attack on the smaller scales is advantageous, in
JANUARY, 1954] GRESSITT, ET AL—CITRICOLA SCALE 9
that individuals of a suitable size for attack are available for a
longer period.
Only one female specimen of Metaphycus orientalis was ob-
tained in the Japanese exploration. It could not be propagated in
the insectary. The habits of this parasite, as judged from records
of 1922, indicate that it may be an effective parasite of overwinter-
ing citricola. Possibilities of acquiring this parasite from Japan
are being investigated by the Department of Biological Control.
SUMMARY
During the first half of 1951, a search was made in Japan by
the Department of Biological Control of the University of Cali-
fornia for parasites of the citricola scale, Coccus pseudomagnoll-
arum (Kuwana). The population of this scale is very low through-
out Japan, and on Poncirus trifoliata, its preferred host plant, it
appears to be under effective biological control.
Coccophagus japonicus Compere, Coccophagus yoshidae Na-
kayama, Cocophagus hawaiiensis Timberlake, Microterys okttsu-
ensis Compere, and Anicetus annulatus Howard were reared from
citricola scale collected in Japan and sent to California. (No ef-
fective predators were found.) Parasites were studies with regard
to host stages attacked, and were liberated in central and southern
California. The first three species listed above have been recovered
from places of liberation.
LITERATURE CITED
CAMPBELL, Roy E.
1914. A new coccid infesting citrus trees in California (Hemip.). En-
tomological News, 25:222-224.
ComPERE, HAROLD
1924. A preliminary report on the parasitic enemies of the citricola
scale (Coccus pseudomagnoliarum [Kuwana]) with descriptions
of two new chalcidoid parasites. Southern California Academy of
Sciences Bulletin, 23:113-123.
1926. New coccid-inhabiting parasites (Encyrtidae, Hymenoptera) from
Japan and California. University of California Publications in
Entomology, 4:33-50.
FLANDERS, STANLEY E.
1942. Biological observations on the citricola scale and its parasites.
Journal of Economic Entomology, 35:830-833.
Kaussart, M.
1946. Insects nuisibles aux aurantiacées sur les Cotes de la mer
Caspienne [In Persian]. Ent. and Phytopath. Appl. 1:32-38. (With
summary in French.) Review Applied Entomology, 36:387, 1948.
10 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
THE SYNONYMY OF THE ANT APHAENOGASTER
LEPIDA WHEELER
In 1929, only a few months after Menozzi had applied the name Aphaeno-
gaster silvestrii to ants collected in Florida, Wheeler described in the same
journal a Formosan homonym. In March, 1930, Wheeler corrected his homo-
nym, which then became A. lepida. Unfortunately, both Menozzi and Creigh-
ton subsequently proposed nomina nova for A. silvestrii of Wheeler without
noticing that a prior nomen novum existed. The resulting synonymy is as
follows:
APHAENOGASTER LEPIDA Wheeler
A. silvestrii Wheeler, Oct. 1929, Boll. Lab. Zool. Portici 24: 37-40, fig. 3,
worker, male; nec Menozzi, Aug. 1929, Ibid., 22: 282.
_ A. (Attomyrma) lepida Wheeler, 1930, Proc. New Engl. Zool. Club 11: 96,
nom. pro A, silvestrii Wheeler.
A. phillipi Menozzi, 1932, Boll. Lab. Zool. Portici 26: 311, nota, nom. pro
A. silvestrii Wheeler. New synonymy
A. funkikoensis Creighton, 1950, Bull. Mus. Comp. Zool. 104: 152, nota,
nom. pro A. silvestrii Wheeler. New synonymy
Cases of automatic synonymy in the family Formicidae are probably
rather frequent, and their formal recognition will help to relieve the nom-
enclatorial confusion which exists in the absence of an up-to-date synonymic
catalog—W. L. Brown, Jr., Museum of Comparative Zoology, Harvard
University, Cambridge 38, Mass.
BOOK REVIEW
HOW TO KNOW THE SPIDERS by B. J. and Elizabeth Kaston. Published
by Wm. C. Brown Company, Dubuque, Iowa. 220 pages, 552 figures.
“How to Know the Spiders” is another excellent book of H. E. Jaques
Pictured-Key Nature Series, similar in pattern to those already published on
the insects, immature insects, beetles and others. Dr. Kaston and his artist
wife have combined to present one of the finest books suitable for the
naturalist or beginning students of spiders.
In the introductory pages the author gives an interesting account of the
biology of spiders including notes on their food, courtship, habitats, webs and
cocoons. There is a short section on the collection, preservation and rearing
of spiders, and an excellent account on the structures used in classification.
This last section is very well illustrated and is the most complete and easily
understood account on spider classification seen by the reviewer.
The last part of the book consists of an illustrated key to 40 of the 49
families of spiders known in the United States to 190 of the common genera
and 271 of the common species. Only those families which are quite rare are
omitted in order to simplify the key. Included with each species recorded is
an illustration and notes on its size, habitat, and distribution.
The species considered in the book are essentially Eastern with only a
very few of those listed found in the West.—Vincent D. Rot.
JANUARY, 1954] LINSLEY & MACSWAIN—EUCERCERIS ll
OBSERVATIONS ON THE HABITS AND PREY OF
EUCERCERIS RUFICEPS SCULLEN
(Hymenoptera, Sphecidae)
E. G. LinsLey and J. W. MacSwain?
University of California, Berkeley
The genus Eucerceris is confined to the western hemisphere and
twenty-eight species are now recognized from America north of
Mexico (Scullen, 1939, 1948, 1951). Until 1939, nothing had been
published concerning the nesting habits or prey of any of these
species. In that year Scullen (1939:12) published observations on
the habits of Eucerceris flavocincta Cresson nesting in two sites at
Breitenbush Hot Springs, Oregon, in July, 1934. The females were
provisioning their nests with the weevil, Dyslobus lecontei Casey.
Scullen also reported that Bridwell had observed the same species
two years previously at Detroit, Oregon, preying upon Dyslobus
segnis Le Conte. In the same publication (Scullen, 1939:40) records
the capture in North Dakota of a female of Eucerceris superba
Cresson carrying a specimen of Ophryastes sulcirostris (Say). The
latter is an otiorhynchine weevil related to Dyslobus.
Eucerceris ruficeps Scullen (1948) was described from females
collected at Antioch, California, and the observations reported here
were made at the type locality in the fall of 1952.
The general area in which Eucerceris was encountered is the
sand dune region just east of Antioch, along the south shore of the
San Joaquin River. Although most of the area is covered by loose
and shifting sand, occasional hard-packed areas occur throughout.
in three such areas, the authors discovered six females of FE. ruficeps
which had appropriated abandoned burrows of the Halictine bee,
Lasioglossum (Sphecodogastra) aberrans (Crawford) ?.
This bee nests throughout the area in late spring and early
summer and its burrows are borrowed, later in the summer, by a
number of other bees and wasps. Each burrow of the bee consists
of a single vertical shaft which varies in depth from about thirty to
forty-five centimeters.
The burrows of the Eucerceris exhibited the following features:
About one centimeter within the entrance the female wasp con-
structs a thin plug across the burrow with a small passage through
1 The writers wish to express their appreciation to G. A. Marsh for assistance
in making some of the field observations reported here.
2 Identified by P. D. Hurd, Jr.
12 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
one side of the plug. At this depth the diameter of the burrow is
about six millimeters, the hole in the plug about three millimeters.
The wasp also constructs a loose plug of moist sand at a depth of
twenty to twenty-three centimeters and at the same point constructs
a lateral tunnel away from the original bee burrow. The lateral
unnel continues downward at angles of from thirty to sixty degrees
with the vertical axis. The total length of the lateral tunnel varies
considerably in different burrows but usually terminates at a depth
of from 29 to 42 centimeters. Another plug of moist sand about
four centimeters in length is constructed near the bottom of the
lateral tunnel and the female wasps pack the weevils which they
collect into this plug. Since the weevils in the plugs are always able
io move, those in the cells immobile, it is presumed that the wasps
either do not paralyze them until they are ready to place them in a
cell or that the sting has a delayed effect upon the nervous system.
Females were never seen in the process of capturing weevils but
some data are available on the plant relationships of the two
weevils involved. Adults of the weevils, Dysticheus rotundicollis
Van Dyke and Sitona californicus Fahrens, do not occur on the
same species of plant. Both males and females of Dysticheus oc-
curred near the nesting site on flowers of the composite, Gutierrezia
californica T. & G. In another area they were found both on
Gutierrezia and less commonly on another composite, Senecio
douglasit D.C. Sitona were collected only from Lotus scoparius
(Nutt.) Attley, although they may well occur also on other legumes
growing in the locality. Both species of weevils were active in early
August, when observations were made, but specimens of Sitona
appeared to be less common than Dysticheus. In addition, the three
Eucerceris burrows which were excavated contained a total of 106
Dysticheus and 82 Sitona.
The first burrow excavated contained a female wasp in fresh
condition and four cells at depths of 28 to 31 centimeters. The con-
tents of three of the cells had molded while the fourth cell contained
a cocoon and living larva. One of the moldy cells contained only .
6 Dysticheus, the other two, 15 each. The cell with the cocoon had
fragments of 14 additional Dysticheus. The absence of cells con-
taining freshly captured weevils raises some question as to just
when the provisioning of the cells took place, although their asso-
ciation with the Sphecodogastra burrow establishes them as having
been provisioned in the current year.
JANUARY, 1954] LINSLEY & MACSWAIN—EUCERCERIS 13
The second burrow was located when a female carrying a
Dysticheus alighted about three feet from the first burrow which
was being excavated at the time. This female was later captured,
along with a second female, at a depth of about 20 centimeters in
the lateral tunnel. Two moist sand plugs containing weevils were
also encountered. The first at 29 centimeters contained two living
Sitona, the second at 39 centimeters contained eight living Di-
sticheus. Four cells associated with the burrow were also excavated.
One cell at 30 centimeters had been provisioned with eleven
Dysticheus which had been destroyed by Tachinids. Another at the
same depth contained a living larva in its cocoon surrounded by
the remnants of 15 Dysticheus. The third cell at 36 centimeters also
contained a cocoon and fragments of 2 Dysticheus and 20 Sitona.
At 38 centimeters the fourth cell with 1 Dysticheus and 12 Sitona
had been destroyed by Tachinids. At a depth of 21 centimeters,
where the lateral branch originated, 10 puparia were found in the
earth to one side of the burrow. Since six of these were pale yellow-
brown and four were larger and dark reddish-brown it seems
apparent that more than one species of parasitic fly was attacking
this host. Unfortunately neither of the female wasps could be asso-
ciated individually with the weevils stored in the plugs or in the
cells.
A third burrow was discovered about a foot away from the
second while the second burrow was being excavated. The contents
of four cells and part of the contents of a fifth cell were uncovered
at depths of 36 to 42 centimeters. One cell with a Eucerceris
cocoon had been provisioned with 15 Dysticheus. Adult wasps had
emerged from the other four cells which had been provisioned as
follows: (1) 18 Sitona, (2) 16 Sitona, (3) 3 Dysticheus and 11
Sitona, (4) 1 Dysticheus and 3 Sitona (incomplete cell).
Unfortunately the rarity of this species and the limited time at
our disposal permitted only these few observations. However, the
data suggest that the Ewcerceris wasps search for their prey on a
habitat basis and that variations in provisions are due to partially
exhausting one of the available sources. Furthermore, although
this species is known at Antioch from about a dozen females col-
lected in August and September, the burrow evidence might be
interpreted to indicate that the species is double-brooded.
14 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
LITERATURE CITED
Scuten, JJ. A.
1939. A review of the genus Eucerceris (Hymenoptera: Sphecidae).
Oregon State Mon. Studies Ent., 1:7-80, figs.
1948. New species in the genus Eucerceris with notes on recorded species
and a revised key to the genus. Pan-Pacific Ent., 24:155-180, figs.
1951. Tribe Cercerini in: Muesebeck, Krombein and Townes, Hymen-
optera of America north of Mexico. U. S. Dept. Agr., Agr. Mon.,
2:1004-1013.
Book REVIEW
THE ANTS OF CALIFORNIA, by Thomas W. Cook, Pacific Books, Palo
Alto, Calif., XVI—462 pp., 92 figs. 1953. $10.00.
The reader is referred to the review of W. L. Brown and E. O. Wilson* for
their reactions as ant specialists to this book.
In preparing this impressive, well printed book the author had a very
sincere and generous purpose in mind. He wanted to provide something
useful for the amateur who is often discouraged by the scattered and at times
unavailable literature in a field. However, amateurs faced with this problem
in studying the ants of California are at present almost non-existant and this
book will do little to encourage the development of more. Indeed it may do
much to discourage them. For one thing, the novice will be baffled at the
outset by the lack of an adequate means of identifying ant subfamilies and
genera. Cook offers three pages of line drawings of ant profiles to fill this
need. Apparently the beginner is expected to compare the ant specimen in.
hand with the drawings and by trial and error arrive at a higher group
identification. This is a fine idea but the beginner who needs such help is
the one least likely to note the often slight critical differences (if any)
apparent in these drawings.
Dr. Cook obviously has a great reverence for original descriptions and
those he calls “revised descriptions” by subsequent workers. The great bulk
of the book is due to the transcription and republication of these often
useless combinations of words. It is most unfortunate to confront a beginner
with such descriptions for many of them are of little value even to an expert.
Dr. Cook’s “naturalists of California,” to whom he dedicates his book, would
have been much better served by a standardized, modern redescription of
each ant species together with adequate keys. This, however, would have
resulted in a much smaller book.
Cook apparently assumed that the amateur is only interested in iden-
tification for little or no mention is made of such things as the technique
of studying ants, making artificial nests, and conducting much-needed bio-
logical studies.
In short, the needs of California ant students are far from adequately
satisfied by this book. One must commend the author, however, for his well
meant purpose, the effort involved in transcribing the scattered work of
others, and the personal expense in getting it published.—E. S. Ross.
* Ent. News 64 :163-164, 1953.
JANUARY, 1954] _ DAY—MAYFLIES 15
NEW SPECIES AND NOTES ON CALIFORNIA
MAYFLIES. II
(Ephemeroptera)
W.C. Day
1021 Hubert Road, Oakland, California
The present paper is given to describe several new species of
mayflies reared from nymphs collected by the author and his wife,
Helen L. Day, on streams of northern California, to record the
collection of species not heretofore taken in California, and to note
new synonyms in the Ephemeroptera.
Ephemerella levis Day, new species
(Figures 1, 2, and 3)
Male imago (in alcohol)
Length: Body 7.5 mm.; forewing 7.5 mm.; foreleg 6.25 mm.; tails 8 mm.
Head: Pale yellow, widely washed with black; nasal carina and frontal mar-
gin white. Antenna pale smoky, basal segment brown and second segment
pale. Ocelli milky white, ringed with black at base. A pair of narrow, black
submedian stripes extend forward from posterior margin of head to median
ocellus. Eyes large, orange, with lower portion black. Thorax: Pronotum pale
yellow, extensively but lightly washed with black; a wide, black U-shaped
mark, opening toward median line, parallels the margins on each side.
Mesonotum pale yellow, median suture dark; a pair of short, dark dashes in
antero-lateral corners; lateral areas of scutellum and entire metanotum, pale
golden brown. A wide, V-shaped brown mark below base of forewing, an-
terior to coxa of middle leg. A prominent dark spot anterior to coxa of hind
leg. Entire sternum golden brown, ganglionic areas marked with black on
each of the thoracic segments. Legs: Yellowish white, foretibiae faintly
smoky. Coxae, trochanters, and tarsal segments of middle and hind legs
finely margined with hair-line of black; tibiae smoky at base. All tarsi with
first segments faintly dark basally. Wings: Hyaline, stigmatic area of fore-
wing milky white. Wingveins clear, colorless; a dark mark on subcosta near
base. A wide, purplish black stripe lies between costa and subcosta, extend-
ing from humeral brace to base of wing. Axial cord of forewing dark purple.
Abdomen: Segments 1-6 hyaline white, 7-10 opaque yellowish white.
Tergites 3-7 with wide, dark bands on median portions of anterior margins;
from terminals of these bands, a pair of short, wide, dark submedian bands
direct themselves toward the median of posterior margin, but do not attain
it. Central portions of tergites lightly surfaced with black. Tergites 1-9
marked with short, dark dashes or a pair of dark spots on each tergite on
lateral margin just above pleural fold. Pleural fold pale. Ganglia darkened
on sternites 1-7; dark stripes on lateral margins of sternites 1-9. Genitalia:
Forceps and penes pale, smoky at tips. Tails: White, strongly banded with
black at each joining.
Nymph (in alcohol)
Length: Body of male 7.5 to 8.0 mm.; female 7.5 to 8.5 mm. Head:
Smooth, pale yellow, irregularly mottled with dark brown. Maxillary palp
16 THE PAN-PACIFIC ENTOMOLOGIST | VOL. xxx, NO. 1
fairly well developed for nymph of serrata group. Thorax: Pale yellow, ir-
regularly mottled with dark brown anterior to wing roots. Sternum variably
pale yellow, pale brown, or mottled brown. Ganglionic areas usually marked
with black. Legs: Pale yellow, strongly marked with brown. Anterior surfaces
of coxae brown. Trochanters pale, with large brown spot on ventral surface
of each. Femora pale, with wide, brown bands near ends, on anterior surfaces
only. Tibiae pale, each with wide, brown band at middle and at basal joining.
Tarsi brown, each with pale band near distal end. Claws brown, 4—7 denticles
on each. Abdomen: Without paired dorsal spines. Posterior margins of
tergites 5—7 slightly sinuate. Tergites gray brown with darkened lateral areas
and dark anterior margins on 1-7. In male nymph, tergite 5 is often pale.
Abdominal segments 3-9 with well developed, flattened lateral extensions,
each of which bears a postero-lateral spine; when viewed from above, the
lateral spines of tergite 8 appear very short; the spines of tergite 3 are
small but well formed. Sternites pale with ganglionic areas darkened; a
single row of curved, brown marks along lateral margins. On well marked
specimens, a row of four dark spots in a line paralleling and close to anterior
margin of each sternite. Gills: Borne on segments 3-7. Tails: Alternately
white and brown, each joining narrowly dark; a whorl of spines at each
joining.
Holotype: Male imago; reared from nymph collected by the
author on CaPELL CrEEK, Napa County, CaLirornia, June 14,
1952; in collection of the California Academy of Sciences. Para-
types (all topotypical) : 1 & in Canadian National Collection; 1 3
in collection of Cornell University; 1 ¢ in collection of G. F.
Edmunds, Jr.; 3 & in author’s collection. Nymphs: 35 nymphs
collected on Capell Creek on June 14, 1952, 40 collected on Capell
Creek on May 20, 1950, and 25 collected on Sulphur Creek, Sonoma
County on July 15, 1950. Nymphs have been sent with the male
imagos listed above.
Ephemerella levis Day belongs to the serrata group of Ephemer-
ella, and the male adult is identical in general appearance, macu-
lation, and structure of the genitalia with E. micheneri Traver;
however, the foretibia of E. levis is 50% longer than the forefemur,
while that of E. micheneri is twice as long, these proportions being
constant in all specimens examined. When describing the adults of
E. micheneri in 1934, Dr. Traver tentatively associated the nymphs
of this species with imagos taken at the same time and place; the
writer has reared adults of E. micheneri from nymphs, and can
confirm Traver’s association of nymph and adult as being correct.
The nymph of E. micheneri has distinct and well formed sub-
median, paired dorsal spines on tergites 2-8, and postero-lateral
spines on segments 4-9. The nymph of E. levis has no dorsal
JANUARY, 1954] DAY—MAYFLIES 17
PLATE I
Fig. 1. Ephemerella levis, genitalia, ventral aspect; Fig. 2. Ephemerella
levis, penes, lateral aspect; Fig. 3. Ephemerella levis, tergites of nymph;
Fig. 4. Ephemerella soquele, abdomen of nymph, lateral aspect; Fig. 5.
Ephemerella soquele, tergites of nymph.
18 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
spines, and bears postero-lateral spines on segments 3—9. In both
species, the postero-lateral spines of segment 8 seem lacking when
viewed from above. The lateral spines of EF. micheneri nymphs are
edged with strong, short spines; those of E. levis are softer, longer,
and hair-like.
E. levis nymph is the exclusive western member of the serrata
group lacking dorsal abdominal spines. On Capell Creek, the
nymphs of both E. micheneri and E. levis are plentiful, and are
found in shallow, slowly running water, resting on sandy bottoms;
in this stream, the nymphs of E. micheneri mature about two
weeks prior to those of E. levis. On Sulphur Creek, nymphs of
E. levis were numerous, but FE. micheneri could not be found.
The association of nymph and adult was established through
rearing.
Ephemerella soquele Day, new species
(Figures 4 and 5)
Nymph (in alcohol)
Length: Body 7.5 to 8 mm.; tails 3.5 mm. Head: Vertex pale with a pair
of wide submedian pale brown stripes from ocelli to posterior margin; fronto-
clypeus dark brown. Lateral margins of labrum black. Antero-lateral portion
deeply cut away, exposing mandibles almost to base. Thorax: Pronotum pale,
with a few brown spots; anterior and lateral margins straight and posterior
margin slightly emarginate; a pair of low, blunt tubercles near median line,
one on each side. Mesonotum pale, the developing scutum of the adult out-
lined in black; a pair of wide, dark submedian curved stripes extend the
full length of the segment. Legs: Trochanters and coxae dark; femora pale,
basally dark-marked and smoky. Tibiae pale, dark banded near apical ends,
and femoro-tibial knees dark. Tarsi dark brown, narrowly pale basally. Claws
pale smoky brown. Abdomen: Prominent lateral extensions on segments 3-9,
each with postero-lateral spine; abdomen widest at segments 5 and 6; the
postero-lateral spines of segment 3 are small, but well formed and distinct.
Fine, sharp-pointed submedian abdominal spines are borne on tergites 2-9,
being longest on tergites 6 and 7; these spines are elevated from the dorsal
plane of tergites 2-4 about 60 degrees, but progressively decrease this angle
to about 10 degrees on tergite 9. Tergites 1-5 pale, with lateral areas widely
dark brown; tergites 1-5 with median brown areas. Tergites 6 and 7 solid
dark brown, with a pair of small pale areas on anterior margins, one on each
side. Tergite 8 with median area pale, dark brown on each side. Tergites
9 and 10 wholly pale. Lateral extensions dark brown, postero-lateral spines
pale. Sternites dark brown, 8 and 9 sometimes pale with a few dark markings.
Sternites with short hyaline-white submedian dashes based on anterior
margins of 2-9; a single row of short dark dashes usually along lateral border
at bases of lateral extensions. Gills: Borne on segments 4-7, those on 4-6
being semi-operculate; rudimentary gill on segment 1. Tails: Fringed with
hairs on each side, hairs longest at middle, nearly bare at tips. Tails pale,
tips dark.
JANUARY, 1954] DAY—MAYFLIES 19
Holotype: Male nymph; collected by Helen L. Day and the
author at Soquel Meadow, Wittow Creek, Maprra County,
CALIFORNIA, on July 14, 1951; in the collection of the California
Academy of Sciences. Paratypes: 4 nymphs in California Academy
of Sciences collection; 4 nymphs in Canadian National collection;
4 nymphs in Cornell University collection; 4 nymphs in G. F.
Edmunds, Jr. collection. 20 nymphs in author’s collection.
Ephemerella soquele Day belongs to the simplex group of this
genus, and is most closely related to E. margarita Needham. In E.
margarita, the paired dorsal abdominal spines are very short and
are borne on segments 3-9; in E. soquele, these paired spines are
borne on tergites 2—9, and are much larger and longer, those on
6 and 7 being more than one-fourth as long as the tergites on which
they are located. The postero-lateral spines on E. margarita are
found on segments 4-9; in FE. soquele these spines are longer, more
acute, and found on segments 3-9. The middle and hind legs of
E. margarita are comparatively shorter than those of E. soquele.
The outer margins of the mandibles of FE. margarita are almost
straight, while those of E. soquele are widely convex.
On Willow Creek, the nymphs of E. soquele were taken on a
shallow, sandy bottom at the quiet, warm edge of a large pool.
Rhithrogena decora Day, new species
(Figures 6, 7 and 8)
-Male imago (in alcohol)
Length: Body 7.0 mm.; forewing 7.84 mm.; foreleg 5.6 mm.; tails 16.8
mm. Head: Pale yellow brown, nasal carina darker; frontal margin widely
hyaline, speckled with fine, black spots, these spots larger and closer together
in median portion. Ocelli black, centers milky. First joint of antenna short,
pale, with white surrounding base; second joint longer, pale with dark tip,
flagellum smoky with dark tip. Eyes contiguous, pale yellow brown, lower
portions black. Thorax: Pronotum pale yellow, a short, wide, purple black
stripe on medial portion of posterior margin. Mesonotum pale yellow, postero-
lateral areas washed with pale brown; inner parapsidal and median furrows
marked finely with black; scutellum and postscutellum dark brown; the
median dorsal surface of scutellum and median area of scutum immediately
anterior, chalky white. Scutellum of metanotum pale with four dark spots;
postscutellum dark brown. Pleura pale yellow and chalky white, prominently
marked with three wide purple black stripes, as follows: from the anterior
point of attachment of wing base, a wide stripe extends forward to pronotum;
from the same point of origin, a second wide stripe extends obliquely down-
ward and across foreleg above forecoxa; posterior to and paralleling this
latter stripe, another stripe extends from wing base down under the foreleg,
terminating on the prosternum. A short, wide purple black stripe above each
coxa. Legs: White, foreleg with femur yellowish, tibia and tarsi faintly
20 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
darker. Coxae each with black spot on apical margin. Femora finely margined
with black at basal joining, and dark banded at distal end; strongly marked
with short, black, longitudinal stripe at middle of anterior surfaces. Tarsal
joinings finely black. Claws somewhat darkened. Wings: Clear and iridescent ;
longitudinal veins light gray, crossveins colorless; humeral brace blackish
brown except for short portion near and at costa. Stigmatic area of the
forewing, milky white. Of the 15-18 crossveins of the stigmatic area, three
or four are usually forked or anastomosed, while numerous specimens have
these crossveins simple and unforked. Abdomen: Tergite 1 purplish brown,
anterior margin white; 9 and 10 chalky white. Tergites 2-8 washed with
purplish brown, posterior margins darker, marked with hyaline white
pattern as follows: large triangles in the four corners; paramedian spots
one-quarter distant from posterior margin; wide, curved stripes based on
anterior margin almost reaching paramedian spots; a narrow median stripe.
Sternites 7-9 largely chalky white; 1-6 hyaline white. Genitalia: Forceps
and penes smoky. Tails: Smoky, lighter at tips; a few sections at base faintly
dark ringed at joinings.
Female imago,. (in alcohol)
Female slightly larger and much paler than male, the abdomen being
a light, rosy purple.
Nymph, (in alcohol)
Length: Body of male 6.0 mm.; female 7.0 mm. Head: Concolorous
blackish brown, posterior margin paler; epicranial sutures hyaline white.
Thorax: Notal surfaces, including wingpads, blackish brown, with a solid
white band across posterior half of mesonotum and bases of wingpads; near
anterior border of this white band, a pair of small, circular dark spots near
lateral margins, one on each side; a narrow white median stripe extends the
full length of both segments. Legs: Femora medium brown, anterior surfaces
with large white area on basal half, and smaller white area at distal end; in
middle of basal white area, a large black spot and 4-5 tiny spots; dorsal
edge with numerous spines. Tibiae smoky. Tarsi pale, distally dark banded.
Claws smoky. Abdomen: Tergites 1-4 medium brown, 6-10 blackish brown.
Tergite 5 white, lateral margins widely dark brown; posterior third of tergite
4 and anterior third of tergite 6 sometimes white. Small paramedian dark
spots usually found on tergites 3 and 4. Spiracles marked with large dark
spots. Posterior margins of tergites 1-10 set with numerous fine denticles.
Sternites brown, very pale on sternite 1, progressively darker to sternite 9
which is very dark; lateral margins blackish brown; a short, black stripe in
median portion, parallel and close to each posterior margin; half-way
between lateral margins and median line, and parallel to latter, a long,
narrow white stripe; oblique white dashes are based on anterior margins
near median line; paramedian white spots usually on stenite 8. Gills:
Lamellae translucent white, tracheae smoky; fibrillae smoky. Lamellate gills
1-6 “eared”, the “ear” of gill 1 being very small, and those of 3-5 propor-
tionately very large. Tails: White.
Holotype: Male imago, collected by author and Helen L. Day
on Hat Creek, Suasta County, Catirornia, July 21, 1953; in
collection of California Academy of Sciences. Allotype: Female
JANUARY, 1954] DAY—MAYFLIES. 21
PLATE II
Fig. 6. Rhithrogena decora, genitalia, ventral aspect; Fig. 7. Rhithrogena
decora, third nymphal gill; Fig. 8. Rhithrogena decora, fifth nymphal gill;
Fig. 9. Paraleptophlebia cachea, third nymphal gill; Fig. 10. Paraleptophlebia
gregalis, penes, ventral aspect; Fig. 11. Paraleptophlebia cachea, genitalia,
ventral aspect.
ae THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 1
imago, same data. Paratypes (all topotypical): 3 o in Canadian
National Collection; 3 & in Cornell University Collection; 3 3
to G. F. Edmunds, Jr.; 65 S in author’s collection. Nymphs: 50
nymphs collected between Emigrant Crossing and Boundary Camp
on Hat Creek, July 15 to July 30, 1953. Nymphs have been sent
with the male imagos listed above. The association of nymph and
adult was established through rearing.
Diagnosis: Rhjithrogena decora Day is of the brunnae type,
and is much smaller than any Rhithrogena found in California to
date. The nymph is recognized by the wide white banding of the
thorax which contrasts strongly with the small dark body. This
species seems quite tolerant of temperature differences, nymphs
being well developed in various sections of Hat Creek that varied
from 50° to 62° F. measured at 3:00 P. M. Nymphal emergence
occurs from 5:00 to 6:30 P. M., and the adults are attracted to
light.
R. decora occurs in close association with what I now refer to as
Rhithrogena californica, n. sp., a medium brown species very
closely related to R. doddsi. During the last week in July, 1953, the
last of the R. decora were emerging at the same time as the first of
the R. californica were emerging.
Compared to other California Rhithrogena, R. decora seems
most stable in the form and spining of the penes. In all specimens
examined, the arms of the penes are narrowed and rounded at the
tips, and slightly divergent; one strong mid-ventral tooth is found
on each arm, and the apical spines, which can be seen only at high
magnifications, are little more than fine, scattered hairs.
Paraleptophlebia cachea Day, new species
(Figures 9, and 11)
Male imago (in alcohol)
Length: Body 9.0 mm.; forewing 9.0 mm.; foreleg 9.0 mm.; tails 13.0
mm. Head: Fuscous, frontal margin widely translucent pale brown; a wide,
pale brown median stripe on vertex. Eyes almost contiguous, pale with lower
portion black. Ocelli milky white, bases black. First two segments of an-
tenna brown, flagellum dark smoky, tips white. Thorax: Pronotum brown,
median portion of anterior and posterior margins and median line with black
stripes. Mesonotum fuscous, lateral and anterior margins yellow marked with
fuscous; margins and area anterior to scutellum black. Sclerites of pleuron
dark brown, membranous areas yellow. Metanotum dark brown with black
markings. Legs: Femora medium golden brown, forefemur darkened at distal .
end. Tibiae light brown; tarsi pale. Wings: Faintly milky, stigmatic area
light brown tinted and translucent. Wing veins yellow brown, progressively
paler toward posterior margin. Abdomen: Tergite 1 dark brown; 7-10
JANUARY, 1954] DAY—MAYFLIES 23
medium golden brown; 2-6 yellow brown. Anterior margins of tergites and
geminate stripes along pleural fold smoky; a fine black mark from spiracles
to postero-lateral corners. Tergites 2-10 with median dark stripe and short
oblique dark dashes from a point near median of anterior margin. Sternites
1 and 8 medium brown with small, dark paramedian spots. Sternite 9
with dark brown W-shaped mark based on anterior margin, occupying about
one-half the area of this sternite; remainder of sternite 9 white. Sternites
2-7 pale yellow brown, anterior margins usually dark; small paramedian
dark spots present, as well as very short dark oblique dashes based close to
anterior margins. Ganglionic areas of sternites 2-7 usually very faintly brown
tinted. Genitalia: Forceps base, forceps and penes light, bright brown. Tails:
Yellow brown, paling distally; joinings narrowly marked with red brown.
Female imago (in alcohol)
Female imago larger and lacking strong color contrasts of male imago.
Head and mesonotum medium dark brown; abdomen more reddish and con-
colorous than male imago. Abdominal markings as in male; wing veins
heavier and stronger in color than male, being dark red brown.
Nymph (in alcohol)
Length: Body of male 8.0 mm.; female 9.0 mm. Head: Dark red brown,
white areas laterad and cephalad of ocelli. Antenna pale at base, darkening
distally, 5 mm. in length. Thorax: Notum dark red brown, anterior margins
of pronotum and mesonotum black. Developing scutellum of mesothorax
black. Legs: Coxae and tronchanters dark brown. Femora and tibiae pale
brown. Tarsi dark brown. Claws dark at base, white tipped, with 18-21 fine
denticles on inner margin of each. Ventral margins of all segments closely
set with fine spines, those of dorsal margins being coarser and less numerous;
a ring of strong spines near apical margins of tibiae. Abdomen: Dark red
brown, unmarked; overlapping of tergites gives appearance of wide black
posterior margins of these. Sternites pale yellow brown, very widely dark
brown laterally; anterior margins narrowly black; dark spots and oblique
dashes of adult can be faintly seen. Sharp postero-lateral spines borne on
segments 8 and 9; short, blunt spines on segment 7. In the nymphal cast
skin, adult pattern of the tergites can be seen clearly. Gills: Broadly lance-
olate, divided almost to base. Tracheae strongly dark, as are a few tracheoles.
Tails: Light brown, pale lateral hairs stemming from joinings.
Holotype: Male imago, reared from nymph collected by the
author and Helen L. Day on small tributary of CacHE CREEK,
Yoto County, CALiFrorNIA, 6 miles north of Rumsey, April 19,
1953; in collection of California Academy of Sciences. Allotype:
Female imago, same data. Paratypes (all topotypical): 1 & in
Canadian National Collection; 1 ¢& in Cornell University Collec-
tion; 1 ¢ to G. F. Edmunds, Jr.; 8 & of April 19, 1953, 6 ¢ and
3 9 of April 26, 1953, and 4 3 of May 17, 1952 in author’s
collection. Nymphs: Nymphs and cast skins have been sent with
types and paratypes listed above; the author retains 8 nymphs and
24, THE PAN-PACIFIC ENTOMOLOGIST | VOL. Xxx, NO. 1
12 cast skins. The association of nymph and adult was established
through rearing. .
Diagnosis: The form of the penes of P. cachea Day shows no
least variation among the male adults collected in two different
years, and serves to separate this species from P. californica and
P. quisquilia. From the latter two species, P. cachea may also be
separated by the markings of the abdomen, and by the blackness
of the dorsum of both male adult and nymph of the new. species.
The nymphs of P. cachea are adapted to unusually high water
temperatures as we found them actively moving about in a small,
slow moving creek of 72° to 76° F. at 3:00 P. M. All other nymphs
of Paraleptophilebia observed by the author emerge at water tem-
peratures of 48° to 60° F.
AMELETUS VALIDUS McDunnough
(Figures 12 and 14)
Ameletus validus McDunnough, 1923. Canad. Ent. 55:50
Through the kindness of Mr. W. J. Brown of the Canadian
National Collection, I have examined the paratype of the above
species, and a slide of the genitalia of same, taken at Banff, Alberta,
on September 30, 1922 by C. B. D. Garrett, and can now state that
the same late season species is also found in California. From
September 26 to September 30, 1953, the author and his wife took
nymphs for rearing from the Upper Truckee River, El Dorado|
County, California, which proved to be A. validus.
In this stream, with water at 52° F. at 3:00 P. M., the nymph
emerges for about two hours starting at 10:30 A. M. The nymph is
found only where well protected from the slightest current at the
water’s edge, between and behind small stones. In emerging, the
nymph crawls entirely out of the water, breaks out of the skin,
dries the wings for up to 21 minutes, and flies high into nearby
trees. The only other mature nymph found in association with
A. validus was Paraleptophlebia debilis.
As an aid to identification, a drawing of the genitalia of A.
validus is given as a part of this paper.
RHITHROGENA FLAVIANULA McDunnough
(Figure 13)
Heptagenia flavianula McDunnough, 1924, Canad. Ent. 56:225
By comparison with a paratype and genitalia slide of the above
species, loaned by the Canadian National Collection, verification
has been made of the collection of R. flavianula on the West Fork
JANUARY, 1954] DAY—MAYFLIES 29
of the Carson River, Alpine County, California. The drawing of the
penes given at the time of description of R. flavianula lacks several
details, so a new drawing is presented herewith.
As is true of other species of the genus Rhithrogena, the upright-
ness or divergence of the arms of the penes cannot be depended
upon as a character for the separation of species, as in several
species of Rhithrogena there is great variation shown in this degree
of divergence. In several species of Rhithrogena there is also found
considerable variation in the size and numbers of teeth and/or
spines on the penes of the male adult.
PLATE III
Fig. 12. Ameletus validus, genitalia, ventral aspect; Fig. 13. Rhithrogena
flavianula, penes, dorsal aspect; Fig. 14. Ameletus validus, penes, lateral
aspect.
EPHEMERELLA HYSTRIX Traver
Ephemerella hystrix Traver, 1934. J. Elisha Mitchell Sci. Soc. 50:212
Ephemerella spinosa Mayo, 1951. Pan-Pac. Ento. 27:122
Examination of the holotypes of E. hystrix and E. spinosa,
together with many specimens of E. hystrix collected by the author
in five counties of California, leads to the conclusion that E.
spinosa is a synonym of E. hystrix. A micro-slide of mouthparts of
E. hystrix from Cornell University Collection bears the same col-
lecting data as the holotype, and shows these mouthparts to be
identical with those of the California species.
26 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
The holotype nymph is faded, but the small denticles on the
abdominal spines are easily seen and precisely like those of the
California specimens in size and placement. Even though faded,
the Cornell holotype shows the distinctive maculation of tergites
and sternites, and the dark pattern of the gills just as they are seen
in all California specimens. The holotype is broader proportion-
ately than some California specimens, and less broad than others.
Like all other species of long-spined Ephemerella collected by
the author, I find considerable variation in the length, curvature
and inclination of the dorsal spines of the California E. hystrix,
and the holotype nymph falls well within the limits of these
variations.
EPHEMERELLA PROSERPINA Traver
Ephemerella proserpina Traver, 1934. J. Elisha Mitchell Sci. Soc. 50:223
Ephemerella yosemite Traver, 1934. J. Elisha Mitchell Sci. Soc. 50:225
E. proserpina was described from a single nymph taken in the
San Bernardino Mts. of California, and E. yosemite from ten quite
immature nymphs from Central and Northern California. I have
examined the above specimens and collected many mature and
immature nymphs of this species from seven California Counties;
recently, a mature specimen of the species, collected in the San
Bernardino Mts., was received from John Belkin. I feel certain
that but one species is involved in all the above material, and that
E. yosemite is a synonym of E. proserpina.
The variation in this species is typical of the nymphs of the
long-spined Ephemerella, and can be demonstrated in the following
analysis of a few characters in twenty-four mature nymphs of E.
proserpina taken from one area of about sixty square feet on East
Fork Carson River on July 3, 1949.
AA 19 have posterior pair pronotal tubercles of equal height
of these
13 with low submarginal pronotal tubercles
6 with higher submarginal pronotal tubercles
12 with margin of 9th. segment flared
7 with margin of 9th. segment straight
BB 5 have posterior pair pronotal tubercles unequal in height
of these
2 with low submarginal pronotal tubercles
3 with higher submarginal pronotal tubercles
5 with margin of 9th segment straight
Male and female adults of E. proserpina have been reared and
will be described in another paper.
JANUARY, 1954] DAY—MAYFLIES 27
PARALEPTOPHLEBIA GREGALIS Eaton
(Figure 10)
Leptophlebia gregalis Eaton, 1884. Trans. Linn. Soc. London, Sec. Ser. Zool.
2:98
Leptophlebia invalida McDunnough, 1926. Canad. Ent. 58:297
In connection with correspondence concerning P. gregalis, Mr.
D. E. Kimmins of the British Museum (Natural History) has
recently cleared in KOH “the genitalia of a paratype which ap-
peared identical with the type in the dried state,” and has supplied
me with a fine drawing, which is reproduced herewith. Mr.
Kimmins’ drawing gives, for the first time, the true appearance of
this taxonomic feature that is essential to the correct separation of
P. gregalis.
Comparison of a Canadian National Collection micro-slide of
the genitalia of a paratype of P. invalida with the above drawing
from Mr. Kimmins, would seem to establish the fact that P.
invalida is a synonym of P. gregalis; the possibility of this syno-
nymy was first suggested by McDunnough in his original descrip-
tion of P. invalida. 3
P. sculleni may also prove to be a synonym of P. gregalis.
P. scullent was described from a now broken-up single male adult,
this specimen having had forelegs missing when described. The
slide of the genitalia made from the holotype of P. sculleni is in
excellent condition, and shows marked similarities to P. gregalis,
notably in the apical lobes of the penes, opening between same,
and the unique, widely curved lower margins of the reflex spurs
shown in the sketch from Mr. Kimmins. The type locality of P.
gregalis was given as “Mt. Hood” and that of P. sculleni as “Cor-
vallis, Oregon”; these localities are about 100 miles apart.
| SIPHLONURUS SPECTABILIS Traver
Siphlonurus spectabilis Traver, 1934. J. Elisha Mitchell Sci. Soc. 50:233
Siphlonurus maria Mayo, 1939. Pan-Pac. Ento. 15:145
The author has examined the type material of S. spectabilis
and that of S. maria, has re-collected and reared adults at the type
localities of both species, and collected specimens of this very
common species in 14 California counties. I feel sure that but one
species of the two is valid, and that S. maria is a synonym of
S. spectabilis.
The original description of the male adult of S. spectabilis was
drawn from the single male adult collected, and it seems probable
to me that this was a teneral or improperly preserved specimen;
28 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
the Mayo description of S. maria perfectly describes the specimens
that I collected on Waddell Creek, the type locality of S. spectabilis.
In connection with several points made in the diagnosis of
S. maria accompanying the species description (P.P.E. 15:148),
S. spectabilis from Waddell Creek and elsewhere is usually dark
red brown in life, forewings are speckled as in specimens from
Amador County, and hindwings nearly or wholly dark orange
brown. The Waddell male adult has the oblique band across the
eyes, and I can find no differences in size of spines of the penes
nor length of the forceps except in proportion to the size of the
specimen, which is variable. Both the color of the abdomen and
hind wing of the male adult varies from one location to another,
and in specimens collected at different times from one location;
there is some reason to believe that the later hatch is smaller and
paler, as in several species of the genus Callibaetis.
New Records of Mayflies in California
The author and his wife, Helen L. Day, have collected in
California several known species not previously reported from this
State, as follows:
Species
Area of
Collected in
type locality California
Heptagenia elegantula Eaton Colorado Stanislaus County
Rhithrogena doddsi McDunnough Alberta Montane
Rhithrogena morrisoni Banks Nevada General
Cinygmula uniformis McDunnough B.G. Coast Range
Iron (Epeorus) albertae McDunnough Alberta General
Iron (Epeorus) dulciana McDunnough OB. C. Sierra Nevada
Iron (Epeorus) longimanus Eaton Colorado General
Siphlonurus occidentalis Eaton Colo. - Wash. No. Calif.
Paraleptophlebia debilis Walker NewS: General
Ephemerella heterocaudata McDunnough Wyo.- Mont. Montane
Ephemerella coloradensis Dodds Colorado Montane
Baetis insignificans McDunnough B. C. Siskiyou County
Baetis intermedius Dodds Colorado Sierra Nevada
Baetis tricaudatus Dodds Colorado Sierra Nevada
Centroptilum convexum Ide Ontario No. Calif. Coastal
REFERENCES
Eaton, A. E.
1883-1888. A revisional monograph of the recent Ephemeridae or may-
flies. Trans. Linn. Soc. London, Sec. Ser. Zool. 3:1—-352, pls. 1-65.
Mayo, VeLtmMa Knox
1939. New Western Ephemeroptera. Pan-Pacific Ent. 15(4) :145-154,
figs. 1-21.
JANUARY, 1954] DAY—MAYFLIES 29
1951. New Western Ephemeroptera II. Pan-Pacific Ent. 27(3) :121-145,
figs. 1-10.
McDunnoueu, J.
1923. New Canadian Ephemeridae with notes. Canad. Ent. 55(2) :50-51,
figs. 1-3.
1924.. New North American Ephemeridae. Canad. Ent. 56(9) :221—-226,
pl. 5.
1926. New Canadian Ephemeridae with Notes. Canad. Ent. 58(12) :296-
302, pl. 3.
Traver, J. R.
1934. New North American species of mayflies. Jour. of the Elisha
Mitchell Sci. Soc. 50:189-254, pl. 16.
NEW SPECIES OF CALIFORNIA MAYFLIES IN THE
GENUS BAETIS
(Ephemeroptera )
W.C. Day
1021 Hubert Road, Oakland, California
Living under conditions of great variety, representatives of the
genus Baetis are found in many types of moving fresh water in
California. The small nymphs have adapted themselves to a wide
range of temperatures and climates, and are taken at all elevations
and at many seasons.
The adult swarms ordinarily consist of a large number of in-
dividuals, and flights often occur in bright daylight. Heavily preyed
upon by birds and insects, the large populations of Baetis are
probably a most important element in their survival.
In the present paper, four new Baetis are described, these pos-
sibly having speciated in the Coastal Valleys of this State.
Baetis leechi Day, new species
(Figures 1 and 2)
Male imago (in alcohol)
Length: Body 4.0 mm.; forewing 4.0 mm.; foreleg 4.0 mm.; tails 9.0 mm.
Head: Pale yellow brown, posterior margin finely black; a broad median
Y-shaped black stripe running cephalad from posterior margin, forks into a
pair of submedian fine stripes which terminate at lateral ocelli. Basal segment
of antenna brown, second segment and filament yellow. Eyes .6 mm. on
longest diameter; stalks .4 mm. in height, measured up the outer side.
Thorax: Pronotum yellow washed with black. Mesonotum bright red brown,
median suture and margins of scutum finely black. Scutellum pale, a pair
of very small submedian pale spots anterior to this pale area; heavily mar-
gined with black. Sternum with brown sclerites outlined in black. Legs:
Coxae brown; foreleg smoky with femur darker; middle and hindlegs pale.
Wings: Hyaline, stigmatic area strongly milky and with 3-5 crossveins
30 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
strongly slanting; a small dark spot at base of each wing. Wingveins entirely
colorless. Paired marginal intercalaries of forewing longest toward costal
margin but lacking in first interspace. Hindwing with three longitudinal .
veins, the third close to and joining hind margin about half-way to tip; no
crossveins or intercalaries; costal projection prominent and strongly curved
much as in Centroptilum. Abdomen: Tergite 1 red brown, 7-10 opaque yellow
with faint cast of brown; 2-6 hyaline palest yellow brown with wide white
hyaline posterior margins; wide whitish median and paramedian stripes full
length of tergites 2-6. Sternites 1-7 hyaline palest yellow. The wide black
geminate lines along pleural fold enclose a strong black spiracular spot and
another dark spot near anterior margin on each segment 1-7. Genitalia:
Second joint of forceps tapered as in the intercaleris group. All segments of
forceps translucent milky white; a fine black lateral line at base of first
segment of forceps. Tails: Translucent milky white; joinings white.
Holotype: Male imago, collected by Helen L. Day and the
author on CoNN CREEK, near RUTHERFORD, Napa County, CALi-
FORNIA, September 24, 1949, in California Academy of Sciences
collection. Paratypes, all topotypical: 5 of in Canadian National
collection; 5 o' in Cornell University collection; 5 ¢& to G. F.
Edmunds, Jr.; 40 & in author’s collection.
Diagnosis: B. leechi Day is the first Baetis with hindwing of
the quilleri type reported from California. B. leechi is quite close
to B. erebus Traver but, apart from color differences, B. leechi is
smaller and lacks crossveins and intercalaries in the hindwing.
In describing this new species, I take pleasure in naming it in
honor of Hugh B. Leech of the California Academy of Sciences.
Baetis diablus Day, new species
(Figures 3 and 4)
Male imago (in alcohol)
Length: Body 9.0 mm.; forewing 8.0 mm.; foreleg 6.5 mm.; tails 17.0 mm.
Head: Dark red brown. Antenna dark red brown, white tipped. Eyes rather
large, moderately elevated; .9 mm. in greatest diameter, stalk .4 mm. in
height, measured up the outer side. Thorax: Pronotum fuscous with a few
pale markings. Mesonotum fuscous; small postero-lateral areas, area anterior
to scutellum and outer parapsidal furrows pale. Scutellum outlined in black.
Sternum fuscous. Legs: Coxae dark brown edged with black. Foreleg yellow
brown. Middle and hindlegs whitish. Wings: Clear hyaline, stigmatic area
of forewing milky. Crossveins of sfigmatic area and longitudinal veins of
forewing pale gray, except those of anal area which are colorless. Crossveins
of stigmatic area irregular, some forking, with short horizontal veins between.
Marginal intercalaries short, a pair of shorter ones in the first interspace.
Hindwing with three long veins, the second vein forking from a point about
three-fifths distant from the base; usually with one intercalary between first
and second vein, and two intercalaries within the fork of the second vein.
Third vein straight, rather long. Costal projection of the hind wing acute.
Abdomen: Segments 1 and 7-10 dark brown; 2-6 hyaline yellow brown,
JANUARY, 1954] DAY—MAYFLIES 31
Fig. 1 Baetis leechi, hindwing; Fig. 2 Baetis leechi, genitalia; Fig. 3
Baetis diablus, genitalia; Fig. 4 Baetis diablus, hindwing; Fig. 5 Baetis alius,
hindwing; Fig. 6 Baetis alius, genitalia; Fig. 7 Baetis sulfurosus, genitalia;
Fig. 8 Baetis sulfurosus, hindwing.
32 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
tergites darker. Tergites with wide dark paramedian stripes, one on each
side. Sternites each with a pair of short oblique dark dashes from middle of
anterior margin. Anterior margins of segments finely dark; posterior margins
white. Genitalia: Distinctly of the moffati type, first and second segments
dark brown, third and fourth smoky brown; third and fourth segments almost
completely fused, their joining marked with a short black line on the outer
side. Tails: Yellow brown, a few basal segments very dark and tips white.
All joinings hyaline white edged with smoky.
Holotype: Male imago, collected by E. I. Schlinger on Mr.
DiaBLo, Contra Costa County, CaLirorniA, April 12, 1952, in
California Academy of Sciences collection. Paratypes, all topo-
typical; 1 & in Canadian National collection; 1 ¢ in Cornell
University collection; 1 & to G. F. Edmunds, Jr.; 2 &, slides of
genitalia and wings in author’s collection.
Diagnosis: Baetis diablus Day is, to date, the exclusive species
of the genus having a forked second hindwing vein combined with
genitalia of the moffati type. The fork of the second hindwing vein
is unlike that of B. parvus or B. devinctus, as it branches much
closer to the distal margin of the hindwing. The fork of the vein in
B. diablus is comparatively shallow and obtuse.
Baetis alius Day, new species
(Figures 5 and 6)
Male imago (in alcohol)
Length: Body 6.0 mm.; forewing 5.5 mm.; foreleg 5.0 mm.; tails 12.0 mm.
Head: Dark brown. Antenna brown with white tip, base ringed with white.
Eyes .75 mm. on longest diameter; stalks .5 mm. in height measured up the
outer side. Thorax: Pronotum blackish brown, paler in median area. Mesono-
tum red brown, scutellum paler; median suture, outer parapsidal furrows,
posterior third of inner parapsidal furrows and margins of scutum finely
black. Metanotum margined with black. Legs: Coxae brown. Forefemur and
foretibia yellowish; all other segments white. Tarsal joinings of middle and
hindleg finely black. Wings: Clear hyaline; wingveins colorless. Stigmatic
area of forewing milky, translucent; crossveins simple, strongly slanting, with
a few short horizontal veins between. Paired intercalaries of first interspace
very long, those of second and third interspace longer than those following.
Hindwing with strong costal projection and three longitudinal veins, the third
very short and close to hind margin; first and second veins convergent dis-
tally; intercalaries not present. Abdomen: Segment 1 and 7-10 dark brown.
Segments 2-6 hyaline, thinly washed with dark brown, anterior margins of
tergites edged with black. A dark geminate line along pleural fold. Each
spiracle of middle segments. strongly marked with outline of small circle,
dark tracheal lines extending onto tergites and sternites from these circles.
Genitalia: Genitalia of the intercaleris type; smoky brown with first segment
dark brown at base. Tails: Milky white, first few basal segments light smoky.
Nymph (in alcohol)
The pale nymph has light. brown dorsum with tergites 5 and 9
JANUARY, 1954] DAY—MAYFLIES 33
pale; tergite 5 with a pair of small dark submedian spots. Anterior
margins of tergites narrowly black. Tergites 1-7 with small black
mark at base of each gill. Femoro-tibial knees black. Middle tail
two-thirds as long as outer tails.
Holotype: Male imago, collected by Helen L. Day and the
author on RusstiAN RIvER, near GEYSERVILLE, SONOMA COUNTY,
CaLirorniA, October 15, 1949, in California Academy of Sciences
collection. Paratypes, all topotypical: 5 o in Canadian National
collection; 5 & in Cornell University collection; 5 ¢& to G. F.
Edmunds, Jr.; 35 & in author’s collection; 50 & collected Novem-
ber 12, 1949, in author’s collection.
Diagnosis: Lacking a tubercle on the inner margin of the basal
joint of the forceps, B. aliws Day, with genitalia of the intercaleris
type, has no known close relative,in California. The adults swarm
some six to ten feet above the water from 10:30 A.M. to 3:00 P.M.
Baetis sulfurosus Day, new species
(Figures 7 and 8)
Male imago (in alcohol)
Length: Body 4.0 mm.; forewing 4.0 mm.; foreleg 3.75 mm.; tails 10.0
mm. Head: Clypeus and face brown; vertex pale yellow with narrow black
Y-shaped mark based on posterior margin and opening forward. Antenna
brown, set in wide white circular sclerites. Eyes .6 mm. on longest diameter ;
stalks .25 mm. in height measured up the outer side. Thorax: Notum blackish
brown. Mesonotum with median furrow and outline of scutum black; scutel-
lum pale at base and a pair of small pale spots anterior to pale area. Tergum
brown, median sclerites outlined in black. Legs: Coxae and trochanters
brown, margins finely black; all other segments light smoky brown. Wings:
Forewing hyaline, stigmatic area milky white. Subcosta and Ri brown; other
longitudinal veins usually finely dark and crossveins pale; crossveins of stig-
matic area often dark and sometimes tending to anastomosis. First interspace
with a single marginal intercalary. Hindwing with costa dark before the
projection, and other veins dark in basal one-third; sometimes with an
intercalary between second and third veins. Abdomen: Tergite 1 blackish
brown; 7-9 paler; 2-6 hyaline smoky brown. Sternite 1 and 7-9 yellow
brown; 2-6 hyaline yellow. Genitalia: Genitalia of the intercaleris type; first
and second segments of forceps pale smoky brown, dark brown at base of
first segment; third and fourth segments pale smoky, edged with black when
seen in yentral or dorsal view; fourth segment one-half the length of third
segment. Tails: Milky white, a few basal segments very faintly smoky.
Holotype: Male imago, collected by Helen L. Day and the
author on the P. C. Hale Ranch, SuLpHuR Creek, Sonoma County,
CaLiForNiA, August 25, 1951, in California Academy of Sciences
collection. Paratypes, all topotypical: 5 & in Canadian National
collection; 5 o in Cornell University collection; 5 ¢& to G. F.
34 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
Edmunds, Jr.; 65 & in author’s collection. 25 ¢ from Capell
Creek, Napa County, California, collected on May 20, 1950, in
author’s collection. ;
Diagnosis: B. sulfurosus Day is quite close to B. thermophilos
McDunnough, the latter described from Yellowstone Park, Wyom-
ing. Apart from being smaller and much paler, B. sulfurosus has
the third vein of the hindwing closer to the posterior margin of the
wing, and the fourth segment of the forceps is proportionately only
about one-half as long as that of B. thermophilos.
B. sulfurosus is undoubtedly the “closely allied species . . . from
Cloverdale, California,’ mentioned by Traver in discussing B.
thermophilos, p. 702, Biology of Mayflies. The confluence of Sul-
phur Creek with the Russian River is about two miles north of
Cloverdale.
With shade temperature at 96° F., B. sulfurosus was found
swarming at noon fully one-quarter mile from the stream. Having
plenty of tree-shade available, this species preferred to swarm in
the open, three or four feet above bare rock and gravel.
BIBLIOGRAPHY
NEEDHAM, J. G., J. R. TRaver and Y. Hsu
1935. The Biology of Mayflies. Comstock Publishing Co., Ithaca, New
York. .
A CHECK LIST OF THE GENERA & SPECIES OF MALLOPHAGA.
By G. H. E. Hopkins and Theresa Clay. Pp. [6+] 1-361. Published by
the Trustees of the British Museum, London. Issued April 1, 1952. Price
£2.
This is a model check list; it is a: pleasure to use. The listing of genera,
and of species within the genera, is alphabetical. All specific names which
have been proposed in a given genus are entered under that generic name.
By using different type faces the authors indicate which names they consider
to represent valid generic or specific concepts, which are synonyms, and
which have been removed to other genera. In the last two instances there are
cross-reference entries. Type species are cited. Hosts are given wherever
known, and corrections suggested for records thought to be erroneous...
The list is based on a study of the world fauna, hence many genera
proposed in regional works are synonymized. It is difficult to tell how many
generic synonymies are original in this book; some are based on unpublished
findings (p. 255: “Although separate from Otidoecus if only the described
species are considered, undescribed species completely bridge the gap between
the two groups.”). Pages 1 to 17 are introductory and explain the authors’
nomenclatorial concepts and working procedure.—H. B. LEecu.
JANUARY, 1954] MALKIN—-EMMESA 35
A NEW NORTHWESTERN MELANDRYID
(Coleoptera: Melandryidae)
Borys MALKIN
University of Washington
Emmesa testacea leeperi Malkin, n. subsp.
Elongate, narrow black except for red coloration of sides of thorax.
Head closely and deeply punctured, frons with shallow fovea in center.
Antennae fuscous, slightly longer than prothorax. Second antennal segment
short, first segment 114 times as long as second, third segment subequal to
first, fourth 114 times as long as third and equal to fifth. Last three segments
rugose longitudinally. Prothorax 1.4 as wide as long, shining, deeply punc-
tured, wider at base than at front, anterior margin truncate, sides arcuate,
expanding posteriorly and attaining greatest width one-third from base. Base
of the prothorax bisinuate, with a shallow longitudinal pit and a notch in
the middle, sides widely red, disc with subquadrate dark cloud. Elytra three
times as long as wide, pubescent, coarsely but regularly punctured, punctures
sub-muricate. Ventral surface black to piceous except posterior half of
inflexed margin of thorax, which is red. Abdominal segments sparsely punc-
tured in middle, more closely on the sides, horizontally finely muricate.
Legs piceous to rufous. Anterior and middle tibia with a spur each, posterior
tibia with two spurs. Tarsal segments: in protarsi first only slightly longer
than second, second one-third as long as the third, third longer than fourth.
In metatarsi first segment extremely elongated almost half length of tibia
and twice as long as second segment which in turn is three times as long as
third. In metatarsi, first segment as long as all others together. Tarsal claws
simple. Length: 9.6 mm. Width: 3.2 mm.
Holotype male: Munset Lake, 4 mi. N. of FLorence, LANE
Co., OrEcon, 14.V1.1950 (B. Malkin and R. L. Leeper), found
floating in lake’s drift. In California Academy of Sciences collec-
tion. Paratypes all males: 1, EucENE, OREGON 23-30.V.1946 (B.
Malkin) ; 1, Genoa Bay, Duncan, British CoLumpta, 14.VI.1928
(W. Mathers), from R. Hopping collection; 1, MANCHESTER,
WASHINGTON 27 May, 1934. The paratypes will be distributed as
follows: Eugene paratype in Malkin collection, British Columbia
paratype in the C.A.S. collection, the Manchester paratype in the
Hatch collection.
The paratypes show considerable diversion from the type, par-
ticularly in the emargination of the posterior end of the prothorax.
The median notch is more pronounced in all of them than in the
type and the Washington specimen is actually deeply bilobed at
the base.
This new subspecies is almost indistinguishable from EF. t.
testacea Van Dyke. The genitalia of the both forms are identical.
36 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
Fig. 1. Male genitalia of Emmesa testacea leeperi.
However, FE. ¢. leeperi is black throughout while E. ¢. testacea is
pale yellow. So far as the available material shows there is a sharp
territorial difference, EF. t. testacea being centered around the San
Francisco bay area in California, while E. t. leeperi is found along
the coast north of the California border. The distributional differ-
ence plus the color difference justify setting apart the new sub-
species.
E. testacea leeperi is named after Dr. R. L. Leeper of the Uni-
versity of Oregon who pointed out to me the type specimens floating
in the lake. Mr. Hugh B. Leech of the California Academy of
Sciences has kindly loaned the British Columbia specimen and also
examples of the typical subspecies and several other closely related
species for comparison, while Dr. M. H. Hatch contributed the
Washington specimen.
REFERENCES
Hatcu, M. H.
1927. Concerning Melandryidae (Coleoptera). Ann. Ent. Soc. Amer.,
20(3) :363-366.
Van Dyke, E. C.
1929. New species of hetermerous Coleoptera. Bull. Brooklyn Ent. Soc.,
23(5) :251-262. (December, 1928, issue of the journal, actually
published January 9, 1929.)
JANUARY, 1954] MICHENER—MEGACHILIDAE 37
DESCRIPTIONS AND RECORDS OF NORTH AMERICAN
HOPLITIS AND ANTHOCOPA?
(Hymenoptera, Megachilidae)
CHARLES D. MICHENER
University of Kansas, Lawrence
In the course of preparing a paper on the Californian species of
certain megachilid bees in cooperation with Dr. P. D. Hurd, Jr.,
of the University of California, several new forms and new dis-
tributional records came to light. The present paper has been
written in order to bring our knowledge of these recently revised
groups up to date and to make certain records and new names
available for use in the above mentioned work.
The specimens recorded and described below come from several
sources. I am indebted to each of the following for the use of
material under his care: Dr. John N. Belkin, University of Calli-
fornia at Los Angeles [U. C. L. A.]; Dr. J. Bequaert, Museum of
Comparative Zoology [M. C. Z.]; Dr. G. E. Bohart, Bureau of
Entomology and Plant Quarantine, Logan, Utah [G. E. B.]; Dr.
G. E. Butler, Jr., University of Arizona [U. A.]; Dr. P. D. Hurd,
Jr., University of California [U. C., B.]; Dr. L. W. Quate, Univer-
sity of Nebraska [U. N.]; Dr. E. S. Ross, California Academy of
Sciences [C. A. S.] and P. H. Timberlake, University of California,
Riverside [U. C., R.]. The letters in brackets are used to identify
ihese collections in the following pages.
Considerable material in the Snow Entomological Museum of the
University of Kansas [K. U.], mostly collected by Dr. R. H. Beamer
or under his direction, is here recorded for the first time.
Hoptitis BULLIFACIES Michener
Hoplitis (Hoplitina) bullifacies Michener, 1947, Bull. Amer. Mus. Nat. Hist. ;
89:274 (female, not male).
This species was described from a few specimens from Inyo
County, California. The holotype is a female. The male available
at the time was only tentatively associated with the females as it
was taken in a different locality. A long series of both sexes now
available from Big Pine Creek, Inyo County, CaLirornia, 7500
feet altitude, June 12 to 20, 1942 (R. M. Bohart) [G. E. B.] shows
that this original association was incorrect. The male originally
placed with bullifacies is another species, named below as H.
1 Contribution number 868 from the Department of Entomology, University of
Kansas.
38 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
(Hoplitina) mazourka. The proper male of bullifacies is described
below:
Male: Length 5.5 to 6.0 mm. Black, metasomal terga one to four red,
sometimes with inconspicuous middorsal black areas; fifth tergum red later-
ally; posterior margins of terga dark testaceous. Clypeus with a strong,
shining, impunctate, median protuberance similar to that of female; clypeal
margin shallowly concave medially, slightly produced and strongly crenulate
sublaterally; inner orbits slightly converging below; antennal scape about
four times as long as broad, pedicel much longer than broad, flagellum reach-
ing middle of scutellum, segments all much longer than broad, first six
subequal in length and slightly more than twice as long as broad, following
segments successively shorter, the last the shortest segment of the flagellum;
mandibular teeth subequal; maxillary palpi as in female. Middle coxae each
with small shining ventral projection or tooth based of trochanter. Sixth
metasomal tergum without lateral teeth; seventh tergum with broad dorsal
concavity, apical margin with small apical notch (fig. 1). First metasomal
sternum with strong protuberance, abruptly declivous posteriorly; second
sternum with posterior margin broadly convex, fringed; third fringed, emar-
ginate medially; fourth and fifth unfringed, slightly emarginate medially;
sixth with deep median pit from which arises a short, blunt process bearing
numerous short hairs; gonoforceps robust, median portions parallel-sided,
apices tapering to blunt points, outer apical margins with long fringes.
Hoplitis mazourka Michener, new species
Hoplitis (Hoplitina) bullifacies Michener, 1947, Bull. Amer. Mus. Nat. Hist. ;
89:275 (male, not female).
This form, a member of the subgenus Hoplitina, is adequately
described in the paper cited above. It differs from true male of
bullifacies, described above, in having short antennae and dentate
lateral margins of the sixth metasomal tergum, as well as in many
other characters.
Holotype male: MazourKa Canyon, Inyo Mountains, Inyo
County, CatirorniA, 7500 feet altitude, on Cryptantha, May 21,
1937 (C. D. Michener) [K. U.].
A second specimen of H. mazourka from Kramer Junction, San
Bernardino County, California, April 20, 1953 (R. O. Schuster)
[U. C., B.] has recently been received. It is not designated a para-
type because of the darker margins of the metasomal terga and the
absence of the weak median emargination of the seventh tergum
but it seems certainly conspecific.
HOPplLiTIs TRUNCATA TRUNCATA (Cresson)
Wyominc: Newcastle, June (M. Cary) [U. N.]. SourH Da-
KoTA: Custer [U. N.]. Nepraska: Glen, Sioux County, 4000 feet
altitude, August 20, 1906, on Cleome (H. S. Smith) ; War Bonnet
Canyon, Sioux County, on Pentstemon (J. C. Crawford) [all U.N.].
JANUARY, 1954] = MICHENER—-MEGACHILIDAE 39
HOPLITIS TRUNCATA MESCALERIUM (Cockerell)
CoLoravo: Ute Creek, 9000 feet altitude, July 11 (R. W. Daw-
son) [U. N.]. Arizona: Williams, 7000 feet altitude, June 15, 1925
(A. A. Nichol) [U. A.]; White Mountains, June 19, 1950 (P. P.
Cook) [K. U.]; Oak Creek Canyon, June 26, 1950 (L. D. Beamer)
[K. U.].
This species has not previously been known west of central
Colorado and New Mexico.
All of the specimens of the species truncata recorded above from
Colorado, Wyoming, South Dakota, and Nebraska exhibit char-
acters intermediate between the two subspecies. The Colorado
specimen (a single female) is nearer to mescalerium while those
from Wyoming, South Dakota, and Nebraska are nearer to truncata.
HOPLITIS PRODUCTA INTERIOR Michener
Cotorapo: Artesia, Moffat County, on Helianthus petiolaris,
July 23, 1950 (C. D. Michener) [K. U.]. Wyominc: Laramie,
some on Pentstemon angustifolium, June 9, 1952 (R. H. Beamer,
L. D. Beamer, W. E. LeBerge) [K. U.]. Uran: Park City, June 11,
1952 (A. E. Wolf, C. H. Winer) [K. U.].
HOPLITIS GRINNELLI GRINNELLI (Cockerell)
Baga Cauirornia: El Mayor, April, 1939 (C. D. Michener)
fK. U.]. Nevapa: Twenty-two miles south of Las Vegas, on
Sphaeralcea ambigua, April 3, 1953 (J. W. MacSwain) [U. C., B.].
HOPLITIS GRINNELLI SEPTENTRIONALIS Michener
IpaHo: Cub River Canyon, Franklin County, on Pentstemon
cyananthus, June 1, 1948 (G. E. Bohart) [G. E. B.]. Uran: Logan,
on Phacelia linearis, June 4, 1948 (G. E. Bohart) [G. E. B.].
Hopuitis UVULALIS (Cockerell)
IpaHo: Willow Flat, Franklin County, July 27, 1950 (C. D.
Michener) [K. U.]. This is a new state record.
HopLitis HYPOCRITA (Cockerell)
ARIZONA: Santa Catalina Mountains, March 13, 1938 (R. H.
Crandall) ; Sabino Canyon, February 24, 1938 (R. H. Crandall)
[all U. A.].
HOPLITIS ALBIFRONS ARGENTIFRONS (Cresson )
Nesraska: War Bonnet Canyon, Sioux County, July 21, 1901
(M. Cary) ; Badlands north of Monroe Canyon, Sioux County, on
Astragalus, June 24, 1901 (M. Cary) [all U. N.].
This is the first record of this form east of the Rocky Mountain
states.
40 THE PAN-PACIFIC ENTOMOLOGIST | VOL. Xxx, NO. 1
HopLitis LAEVIBULLATA (Michener), new combination
Anthocopa (Eremosmia) laevibullata Michener, 1943, Ann. Ent. Soc. Amer.,
36:68 (female).
Hoplitis (Acrosmia) perissocera Michener, 1947, Bull. Amer. Mus. Nat. Hist.,
89:299 (male) (new synonym).
Both sexes of this species were collected in numbers at Pinecrest,
Tuolumne County, Catirornia, July 16, 1952, on a low growing
Nemophila (R. Snelling, J. I. Stage). (An additional specimen
from the same locality was collected on June 29, by J. I. Stage).
The association of sexes indicated by the above synonymy is thus
established.
A female specimen previously recorded from Hanna, Urau,
July 14, 1949 (R. H. Beamer) [K. U.] and another from Logan,
Utah, June 16, 1947 (G. E. Bohart) [G. E. B.] differ from Calli-
fornia material in having the clypeal truncation wider, about equal
in width to the distance from the end of the truncation to the lateral
angle of the clypeus.
The subgenus Acrosmia is more similar to Anthocopa than is
any other American group of Hoplitis. It has the robust body form
typical of Anthocopa, particularly in the female. The first metaso-
mal tergum has the anterior surface flat, not convex as in most
Hoplitis. However, there is a distinct longitudinal sulcus in this
surface, as in Hoplitis. Other features suggesting placement in
Hoplitis are the absence of carinae on the rear coxae and the
presence of a tooth (weak and blunt) on each side of the sixth
metasomal tergum of the male. In addition to H. laevibullata this
subgenus contains H. plagiostoma Michener and the new species,
rufina, described below.
HoP.itis PLAGIOSTOMA Michener
The following record, based on a single male, is the second
known locality for this species. OREGON: Fish Lake, Steens Moun-
tains, 7000 feet altitude, July 11, 1927 (H. A. Scullen) [U.C., R.].
Hoplitis rufina Michener, new species
This is a species of the subgenus Acrosmia which differs from
the other known species by the red abdomen. In the deeply emar-
ginate seventh metasomal tergum of the male this species most
nearly resembles H. laevibullata (Michener) but it differs from that
form morphologically in the rounded median apical projection of
the seventh sternum. The female differs from that of laevibullata
not only in color but in the punctate clypeal swelling, the longer
JANUARY, 1954] MICHENER—MEGACHILIDAE Al
clypeal trunctation demarked by distinct angles, and other char-
acters.
Female: Length 7 mm. (varying to 6 mm. among paratypes). Black with
mandibles apically and under surfaces of flagella slightly brownish, tergulae
brown, metasomal terga red except that sixth is black and extreme sides of
fifth are infuscated (subapical dark band on fifth in specimen from Oregon).
Wings brown, veins and stigma brownish black. Pubescence white, rather
sparse, not forming bands on metasomal terga except laterally on first; sixth
tergum with pale hairs scattered over surface. Head about as long as broad,
inner orbits slightly converging below; clypeal truncation slightly broader
than distance from end of truncation to lateral angle of clypeus, ends of
truncation each demarked by distinct, slightly produced angle and middle
of truncation also slightly produced so that the clypeal margin has three
feeble projections (fig. 3); upper three-fourths of clypeus strongly convex;
clypeus coarsely punctate, the punctures longitudinally elongate, especially
anteriorly, wide smooth interspaces between punctures on median portion
of convexity; remainder of head finely punctured, particularly finely and
closely so on frons; median ocellus twice as far from antennal bases as from
posterior margin of vertex; distance between posterior ocelli equal to dis-
tance from one of them to eye margin and to posterior margin of vertex;
mandibular teeth equidistant; maxillary palpi five segmented, third segment
much longer than the others, which are subequal in length. Mesonotum and
scutellum slightly more coarsely punctate than vertex; mesepisterna more
coarsely so than scutum; enclosure of propodeum granular throughout. Hind
tibial spurs pale brown, curved apically. Abdomen with punctures shallow,
mostly separated by several diameters, but fully as large as those of meso-
scutum; surface between punctures shining but minutely roughened, par-
ticularly on posterior margins of the terga where punctures are weak and
inconspicuous.
Male: Length 6 mm. Coloration similar to female but antennal flagella
paler brown except for dark last segment; tegulae nearly black; fifth and
sixth metasomal terga black except for reddish translucent apices, seventh
black. Pubescence sparse and pale as in female except that face is largely
covered with long white hair (largely worn off in allotype). Head much
broader than long, finely and densely punctate except for hypostomal and
lower genal areas where punctures are widely separated; inner orbits
parallel; clypeus scarcely extending below lower ends of eyes, margin
shining and impunctate, median portion made crenulate by five small con-
vexities of which the median is broadest; median crenulate portion of margin
exceeding lateral portions; antennal scape over four times as long as broad;
last flagellar segment longer and broader than others, produced to one side
to form a pointed process shorter than in laevibullata (process narrowly
rounded in Utah specimen) ; first flagellar segment next in length, longer than
broad; second and following segments about as broad as long; flagellar
segments two to six with some long hairs on lower margin (short, few,
perhaps worn or broken in allotype, long and curved as in other Acrosmia
in specimen from Utah). Thoracic and abdominal sculpturing much as in
female. Sixth metasomal tergum with a tooth at each side, seventh strongly
42 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
bilobed, lobes narrower than emargination between them, the latter deeper
than a semicircle; exposed sterna as in laevibullata but sixth metasomal
sternum with median process rounded, apparently not constricted basally.
Of the six known specimens of this species, no two have been
collected at the same place. As indicated below, some of the speci-
mens are not included among the paratypes because they are from
remote localities and exhibit minor differences from the type series
as indicated in parentheses in the description above.
Holotype female: MapERA County, CatirorntA, 3000 feet alti-
tude, May 27, 1938 (R. M. Bohart) [C. A. $.]. Allotype male:
Big Pine Creek, Inyo County, California, 7500 feet altitude, June
12, 1942 (R. M. Bohart) [C. A. S.]. One female paratype: Pine
Flat, Tulare County, on Viola purpurea, May 3, 1947 (P. H. Tim-
berlake) [U. C., R.].
Three additional specimens are from the following localities:
CatirorniA: Tetley Park, San Bernardino Mountains, on Nemo-
phila, May 23, 1936 (E. G. Linsley) [U. C., B.]. OrEcon: Camp
Abbot, Deschutes County, June 4, 1944 (P. A. Arnaud). Urau:
Logan Canyon, May 27, 1938 (Bischoff) [G. E. B.].
HoPLITIS BISCUTELLAE (Cockerell)
NeEvapDA: Twenty-two miles south of Las Vegas, on compositae
and Sphaeralcea ambigua, April 3, 1953 (J. W. MacSwain) ; six
miles south of Las Vegas, April 6, 1953 (R. F. Smith, J. Linsley)
[all U. C., B.]. Uran: Zion National Park [G. E. B.]. These are
new state records.
ANTHOCOPA ELONGATA (Michener )
Montana: Lake St. Marys, Glacier National Park, June 1, 1938
(E. C. Van Dyke) [K. U.]. WasHincton: Sunrise, Mount Ranier,
July 11, 1934 (O. Bryant) [C. A. S.]. These are new state records.
Anthocopa anthodyta bequaerti Michener, new subspecies
This form is distinguishable from typical anthodyta from Cali-
fornia by the shape of the seventh metasomal tergum in the male,
which has large lateral lobes, as long as the median spine of this
tergum. The lateral margins of the tergum are slightly more convex
than usual in typical anthodyta. In other respects, including the
medially narrowed mandibles of the female and the long white
apical fringe on the fourth metasomal sternum of the males,
bequaerti resembles anthodyta,
Holotype male, allotype female, and two paratypes of each
sex. Box Canyon, Santa Rita Mountains, ARIZONA, on red Pent-
JANUARY, 1954] MICHENER—MEGACHILIDAE 43,
stemon, April 23, 1949 (J. Bequaert) [M. C. Z.]. A pair of para-
types is in the Snow Entomological Museum.
Anthocopa arizonensis Michener, new species
This species of the subgenus Atoposmia is closely related to
A. anthodyta Michener but differs by the largely ferruginous tegu-
lae, the ferruginous tibial spurs, and the more coarsely punctured
posterior part of the abdomen.
Female: Length 7 mm. Agrees with the description of A. anthodyta
(Michener, 1943) and with specimens of that species except in the following
particulars: Clypeus distinctly red along anterior margin, its surface more
convex than in anthodyta, the punctures medially separated by a little
shining ground, a longitudinal median raised line (more noticeable in some
paratypes than in holotype) present; mandibles much narrowed medially but
not quite so much so as in anthodyta, so that length along lower margin is
slightly less than four times shortest breadth; distance from subapical inner
swelling to apex of third tooth much less than shortest width of mandibles.
Tegulae ferruginous, dusky or black anteriorly; tibial spurs ferruginous.
Abdomen with posterior margins of terga broadly transluscent brown;
punctures of abdomen unusually coarse, those of center of second tergum
separated by one to two puncture widths, those of centers of third, fourth and
fifth terga closer, many of them fully as large as largest punctures of
mesoscutum.
Holotype female: GRAND Canyon, Arizona, June 7, 1940
(R. M. Bohart) [C. A. S.]. One female paratype, same data, 7000
feet altitude [U. C. L. A.]; one female paratype, same data, June
5, 1940 [K. U.]. One female paratype: Jacob Lake, Arizona, 8000
feet altitude, June 13, 1940 (R. M. Bohart) [U. C. L. A.].
ANTHOCOPA ABJECTA (Cresson)
Osmia abjecta Cresson, 1878, Trans. Amer. Ent. Soc., 7:103.
Hoplitis mesae Cockerell, 1930, Amer. Mus. Novitates, 397:2 (new synonym).
Anthocopa nigrior Michener, 1943, Ann. Ent. Soc. Amer., 36:54 (female,
not male) (new synonym).
Larger series of abjecta than were available in 1943 show that
the female described as nigrior is indistinguishable from individ-
uals in Utah and Colorado populations of abjecta. The male de-
scribed under nigrior is quite different from the male of abjecta
and probably represents a distinct species whose female is un-
known. It was unfortunate that it was associated with nigrior since
it-was not collected with the female specimens assigned to that
species.
A re-study of the type of mesae, kindly lent for examination by
Dr. M. A. Cazier of the American Museum of Natural History,
shows that it is the male of abjecta, as was suggested earlier
MM. THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
(Michener, 1943). The dark pubescence is nearly all worn off of
the legs and abdomen, but is still recognizable.
Male: Agrees with description of male of alta (Michener, 1943) except
that distance between posterior ocelli is often equal to distance to posterior
margin of vertex and to distance from ocelli to eye margin. Pubescence of
head and thorax entirely pale as in alta but legs with pubescence largely
black or fuscous; abdomen with much fuscous hair, the pale bands incon-
spicuous, sometimes visible only on first tergum, in other individuals evident
en first four terga.
Uran: Park City, on Pentstemon moffatti, June 11, 1952 (A. E.
Wolf, W. E. LaBerge, Cheng Liang) [K. U.]: twenty miles east of
Salt Lake City, June 11, 1952 (Cheng Liang) [K. U.]: Allen
Canyon, July 3, 1950 (G. F. Knowlton, S. L. Wood) [G. E. B.].
CoLorapo: Monarch Pass, July 5, 1949 (R. H. Beamer) [K. U.];
Trout Creek Pass, July 5, 1949 (J. R. White) [K. U.]; Science
Lodge, west Boulder County, July 6, 1939 (U. N. Lanham)
LK. U.]; Beaver Reservoir, on Penstemon alpinus, July 1, 1939
(P. H. Timberlake) [U. C., R.].
Anthocopa hebitis Michener, new species
This species, a member of the subgenus Atopsomia, is related
to A. pyenognatha Michener with which it agrees in the short
maxillary palpi and the ferruginous tegulae and tibial spurs. It
differs from pycnognatha and from all other Atoposmia in the
exceedingly fine and close punctuation of the face, vertex and
dorsum of the thorax, there being no interspaces between punctures.
It also differs from all other Atoposmia in the hind basitarsi; in
the female they are finely and closely punctured, dull, and almost
2.3 times as long as broad. In the male they are somewhat less dull,
2.5 times long as broad. In all other species the hind basitarsi are
shining, rather coarsely punctured, and comparable ratios are 2.5
to 3.0 for females, 3.0 to 4.0 for males. In the male of hebitis the
lateral margins of the sixth metasomal tergum are relatively
straight, not convex as in pyenognatha.
Female: Length 7 mm. Pubescence pale brownish, yellow on under
surfaces of tarsi, whitish on sides of head and thorax. Punctation of head and
thorax fine and close, no interspace between punctures in most areas: punc-
tures of clypeus scarcely coarser than those of frons, those of mesoscutum
somewhat coarser than those of vertex; anterior ocellus somewhat behind
midpoint between posterior edge of vertex and antennal bases: distance
between posterior ocelli slightly shorter than distance from one of them
to eye margin, more distinctly shorter than distance to posterior margin of
vertex; pubescence of genal areas abundant, depressed, and directed forward:
punctation of genal areas particularly fine and close; clypeal truncation
JANUARY, 1954] |= MICHENER—MEGACHILIDAE 45
about as long as distance from its rounded end to lateral angle of clypeus;
mandibles slightly less than three times as long as shortest breadth, tridentate,
subapical dorsal swelling rounded, distant from apex of third tooth by about
one-third shortest breadth of mandibles; maxillary palpi little more than
half as long as first segment of labial palpi, five-segmented but last segment
short and exceedingly minute, third segment longer than the others, first,
second and fourth subequal in length. Dorsum of thorax finely and closely
punctured but somewhat more coarsely so than vertex; mesepisterna more
coarsely punctured than mesoscutum, punctures slightly separated by shining
ground; enclosure of propodeum somewhat roughened above; tegulae reddish
brown, infuscated anteriorly; hind tibial spurs reddish brown, somewhat
curved apically; hind basitarsi dull, minutely punctured, parallel-sided basally,
tapering apically, 2.3 times as long as broad. Abdomen strongly punctured,
the coarser punctures of sides of terga coarser than those of any part of
thorax, punctures of middorsal parts of first three metasomal terga separated
by less than a puncture width in most places and extending almost to posterior
margins of terga; punctures of fourth tergum closer than those of preceding
terga; punctures of fifth and sixth terga finer and about as close as possible;
scopa yellowish white, short, hairs of second sternum not much longer than
length of exposed portion of sternum; apical pubescent bands of terga
broken medially on first three terga.
Male: Length 9 mm. Similar to female in appearance and punctation.
Clypeus but little more finely punctured than rest of head; distance between
posterior ocelli equal to distance from one of them to eye margin and to
distance to posterior margin of vertex; clypeal truncation slightly produced,
demarked by distinct angles, much longer than distance from end of trunca-
tion to lateral angle of clypeus; margin of truncation slightly crenulate,
narrowly impunctate. Punctation of mesoscutum scarcely coarser than that of
vertex. Third metasomal sternum with conspicuous, broad, fringed emargi-
nation; sixth tergum with strong tooth at each side, the apex of which is
distinctly acute, laterally this tergum not strongly convex; seventh tergum
with median tooth slightly exceeding the distinct lateral lobes; posterior
margins of terga much more broadly reddish brown than in female.
Holotype female: MINERALKING, TULARE COUNTY, CALIFORNIA,
July 31, 1935 (G. E. Bohart). This specimen is being deposited at
Dr. Bohart’s request in the California Academy of Sciences.
Because it was not collected at the same place, the male speci-
men, from Huntington Lake, Fresno County, California, August,
1917 (I. McCracken) [C. A. S.] has not been designated as an
allotype.
Anthocopa rubrella macswaini Michener, new subspecies
Female: Length 5 mm. (varying to 4 mm. among paratypes). Agrees
with typical rubrella Michener (from Texas) but is smaller (rubrella ranges
from 5.6 to 7 mm. in length), with the median pair of small lobes on the
clypeal margin broader, each consistently half as wide as the lateral apical
lobes formed by the ends of the clypeal truncation.
Male: Length 5 mm. (varying to 4 mm. among paratypes). Agrees with
typical rubrella except for smaller size.
46 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. l
Holotype female, allotype male, and two female and eight male
paratypes: TWO MILES SOUTH OF BAKER, SAN BERNARDINO CounrTY,
Catirornia, April 4, 1953 (J. W. MacSwain [U. C., B.]. One male
paratype: seven miles north of Vidal Junction, San Bernardino
County, California, April 3, 1951 (P. D. Hurd) [U. C., B.].
The holotype and allotype are placed in the Snow Entomologi-
cal Museum, University of Kansas.
A single male from twenty-two miles south of Las Vegas,
Nevada, April 3, 1953 (J. W. MacSwain) [U. C., B.] is referred
to this subsepcies.
A single male, large enough to be typical rwbrella, is from San
Carlos Bay, Sonora, Mexico, on Dalea, April 8, 1952 (L. D.
Anderson) [U. C., R.].
Anthocopa rubrella rubrior Michener, new subspecies
Female: Length 5 mm. (varying to 4.5 mm. among paratypes). Agrees
with typical rubrella Michener (from Texas) except for the smaller size, the
broader median lobes of the clypeal margin (each of which is nearly as wide
as the lateral apical lobes formed by the ends of the clypeal truncation),
and the larger amount of red coloration, as follows: mandibles except bases
and apices, apical margin of clypeus, tegulae, posterior lobes of pronotum
(black in some paratypes), posterior femora (largely black in some para-
types), inner surfaces of posterior tibiae (black in some paratypes), and
entire metasoma, infuscated on sixth tergum and sternum. (In some paratypes
middorsal areas on fourth and fifth terga, basal portion of sixth tergum and |
entire fifth and sixth sterna black). The pubescence seems denser and whiter
than that of either rubrella proper or macswaini.
Male: Length 5.5 mm. (varying to 5 mm. among paratypes). Agrees with
typical ruwbrella except in coloration, which is as in the female.
Holotype female, allotype male and one male paratype: Hop-
kins WELL, RiversipE County, Catirorni, April 29, 1952 (J. G.
Rozen) [U. C., B.]. One female paratype: twenty-four miles south
of Indio, California, on Dalea mollis, March 25, 1933 (P. H. Tim-
berlake) [U. C., R.]. One female paratype: eighteen miles west of
Blythe, California, on Dalea mollis, April 30, 1952 (P. H. Timber-
lake) [U. C., R.]. One female paratype: Anza State Park, San
Diego County, California, April 23, 1951 (R. C. Bechtel)
[U. C., D.]. One male paratype: Borego, San Diego County, Calli-
fornia, May 2, 1952 (J. G. Rozen) [U. C., B.].
The holotype and allotype are placed in the Snow Entomological
Museum, University of Kansas.
This subspecies is much more different from the Texan rubrella
than is macswaini from San Bernardino County. The latter is inter-
mediate in certain respects. Nonetheless it is possible that rubrior
JANUARY, 1954] §=MICHENER—-MEGACHILIDAE 47
represents a different species but this probably will not be clear
unless rubrior and macswaini are found to occur in the same area.
Anthocopa hurdiana Michener, new species
This form is similar to A. rubrella macswaini, differing in the
simple truncate clypeal margin of the female, the less convex and
less shining upper part of the clypeus of the female, the slightly
narrower genal areas of the female, the positicn of the ocelli
slightly nearer to the posterior edge of the vertex in the female,
and the slightly narrower head in the male.
Female: Length 5 mm. Agrees with the description of A. rubrella
(Michener, 1949) except as follows: Clypeus truncate, truncation shorter
than distance from its end to lateral angle of clypeus; upper two-thirds of
clypeus less convex, its punctures rather close, much larger than those else-
where on head; median ocellus about twice as far from antennal bases as
from posterior edge of vertex; distance between posterior ocelli equal to
distance from one of them to eye margin, much greater than distance to
posterior edge of vertex; genal areas about half as wide as eye, seen from
side. Tegulae brown, infuscated anteriorly; punctation of mesoscutum like
that of vertex, that of mesepisterna slightly sparser. Second metasomal tergum
with black spot dorsally, third largely black dorsally.
Male: Length 5 mm. Differs from the description of A. rubrella as
follows: Inner margins of eyes distinctly converging below.
Holotype female, allotype male, and one female paratype: SUR-
PRISE Canyon, Inyo County, Catirornta, on Dalea fremontii,
April 28, 1953 (P. D. Hurd) [U. C., B.]. The holotype and allo-
type are in the Snow Entomological Museum, University of Kansas.
Anthocopa namatophila Michener, new species
This small black species is a member of the subgenus Phaeosmia,
in so far as can be determined from the female alone. In size and in
the presence of an apical flange, not hidden by a subapical fascia,
on the sixth tergum, this species resembles A. rwbrella Michener,
maryae Michener and hurdiana Michener. It differs from the first
two by the unmodified clypeal margin.
Females: Length 5 mm. Pubescence white, brushes of hair under margin
of clypeus short but rather broad and orange, mandibles with some orange
hair on outer surfaces but not forming a definite brush. Inner margins of
eyes slightly converging below; anterior margin of clypeus produced to a
broadly rounded truncation with rounded ends, length of truncation about
equal to distance from end of truncation to lateral angle of clypeus, produced
anterior marginal area of clypeus not directed forward; head rather finely
punctured, punctures not widely separated, those of clypeus coarser than on
rest of head; upper two-thirds of clypeus but little more strongly convex than
lower third of clypeus and slightly more coarsely punctured than lower third;
lower third with punctures exceedingly close except for the narrow impunc-
48 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
tate apical margin of truncation: anterior margin of clypeus rather broadly
red; anterior ocellus twice as far from antennal bases as from posterior edge
of vertex; distance between posterior ocelli about equal to distance from
one of them to eye margin, nearly twice distance from one of them to posterior
margin of vertex; mandibles red except basally, subapical inner swelling
rather high and obliquely truncate distally, apex of median mandibular tooth
about equidistant between apices of upper and lower teeth; maxillary palpi
short, five-segmented, second and third segments subequal and longer than
any of the others; first segment of labial palpus about half as long as second.
Thorax about as coarsely punctate as head, disc of mesoscutum with punctures
slightly more widely separated than those of vertex; mesepisternum with
punctures slightly finer than those of mesoscutum, more widely separated
than and slightly coarser than those of genal areas; upper portion of enclosure
of propodeum slightly roughened, lower portion shining; tegulae testaceous,
infuscated anteriorly; hind tibial spurs testaceous, slightly curved at apices;
wings faintly dusky. Abdomen distinctly punctured; punctures of central
portion of second tergum slightly finer than those of mesoscutum, separated
by about a puncture width; posterior margins of terga broadly brownish with
a distinct impunctate zone along the margin proper in front of which is a
region of fine punctation; posterior margins of terga with bands of white
pubescence which are not dense enough to obscure the brownish margins of
the terga; sixth tergum without a subapical band of hairs but with scattered
distinct white hairs over entire surface and with a brownish flange along
posterior margin; scopa white.
Holotype female and three female paratypes: SEVEN AND ONE-
HALF MILES SOUTH OF TWENTY-NINE PaLms, CALIFORNIA, on Nama
demissum, May 7, 1949 (P. H. Timberlake) [U. C., R.].
Anthocopa segregata Michener, new species
Anthocopa robustula, Michener, 1943, Ann. Ent. Soc. Amer., 36:71 (Kearsarge
record only).
Specimens of this species have been confused in collections with
A. robustula (Cockerell). They differ particularly in the coarser
punctation of the upper, convex part of the clypeus of the female,
this region being conspicuously more coarsely punctured than any
other part of the head. Also the subapical swelling of the inner
margin of the mandible is weak and gently rounded, not strong and
truncated apically as in robustula. The species is also close to A.
hypostomalis Michener but differs in having the hypostomal carinae
low with the longitudinal portions longer than the transverse
portions.
Female: Length 8 mm. (paratype 7 mm.) Pubescence white, brushes of
hair under margin of clypeus broad, rather long, orange; mandibles without
brushes of orange hair on other surfaces. Inner margins of eyes very slightly
diverging below; anterior margin of clypeus produced to a broadly rounded
truncation with rounded ends, length of truncation about equal to distance
irom end of truncation to lateral angle of clypeus, produced portion of clypeus
JANUARY, 1954] =MICHENER—MEGACHILIDAE 49
not directed anteriorly; head finely punctate except for clypeus which has
punctures much coarser than those elsewhere; upper two-thirds of clypeus
distinctly convex, its punctures separated by one-third a puncture width;
lower flat portion of clypeus with punctures slightly elongated, similarly
separated; margin of clypeus impunctate, rather irregularly roughened; punc-
tures of rest of head but little separated; anterior ocellus slightly behind
midpoint between antennal bases and posterior edge of vertex; distance from
posterior ocellus to eye margin very slightly greater than distance between
posterior occelli and about equal to distance from one of them to pos-
terior margin of vertex; mandible slightly reddish throughout, subapical inner
swelling low and rounded, apex of median tooth ebout midway between
apices of first and third teeth, narrowest portion of mandible slightly more
than one-fourth as long as mandible measured along lower margin; maxillary
palpi five-segmented, second and third segments subequal and longer than
others. Punctures of thorax coarser than those of top of head, those of
Pe
EXPLANATION OF FIGURES
1., Posterior end of abdomen of male of Hoplitis bullifacies. 2, Same,
Hoplitis rufina. 3, Outline of clypeus of female, Hoplitis rufina. 4, Same,
Anthocopa rubrella rubrior. 5, Same, Anthocopa rubrella macswaini. 6, Apex
of mandible, Anthocopa segregata, female. 7, Same, Anthocopa mirabilis, male.
8, Same, Anthocopa namatophila, female. 9, Same, Hopiitis rufina, female.
mesoscutum and mesepisterna separated by about one-fourth a puncture
width or slightly more; enclosure of propodeum roughened and dull laterally
but smooth to upper margin medially; tegulae testaceous; hind tibial spurs
bent apically, testaceous; wings nearly clear. Abdomen distinctly punctured
but punctures much smaller than those of thorax, those of center of second
tergum separated by two to three puncture widths; posterior margins of terga
translucent brownish, very narrowly impunctate, with broad bands of white
pubescence; entire sixth tergum with scattered white hairs; scopa white.
Holotype female: MazourKa Canyon, Inyo Mountains, Inyo
County, CatirorniA, on Parosela fremontii, May 25, 1937 (C. D.
Michener) [K. U.]. Paratype female: near Kearsarge, Inyo County,
May 25, 1937 (E. C. Van Dyke) [C. A. S.].
ANTHOCOPA HYPOSTOMALIS Michener
The male of this species is here described for the first time.
LL
50 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
Male: Length 7 mm. Similar in appearance to female. Pubescence largely
white, that of dorsum of head and thorax yellowish. Inner margins of eyes
distinctly diverging below; clypeus much more finely and closely punctured
than rest of head, densely covered with white pubescence which obscures
surface; anterior margin of truncation shining and crenulate; area behind
ocelli not more coarsely punctate than rest of head; mandibles broader at
level of apex of inner tooth than medially. Tegulae reddish testaceous; upper
part of enclosure of propodeum smooth medially. Abdominal punctation
somewhat coarser than in female but finer than that of a mesoscutum; sixth
metasomal tergum with posterior margin truncated medially, the truncation
continuous with the convex lateral margins, with no emarginations or teeth
or lobes laterally and no projecting flange medially; seventh tergum with
posterior margin slightly and broadly emarginate medially, scarcely exposed
beyond sixth; second and following sterna brown rather than black; second
large, its margin narrowly truncate medially; third with posterior margin
broadly emarginate with a fringe of long yellowish hairs medially; fourth
with posterior margin produced to a small rounded median lobe.
Catirornia: Palm Springs, on Cryptantha barbigera, March
30, 1945 (P. H. Timberlake) [U. C., R.]; Surprise Canyon, Inyo
County, on Dalea fremontii, April 28, 1953 (P. D. Hurd)
PUSG:B:];
ANTHOCOPA HEMIZONIAE (Cockerell)
Mr. P. H. Timberlake has obtained a male of this species,
hitherto known only from the female. It is described as follows:
Male: Length 9 mm. Similar in appearance to female but pubescence
even yellower, particularly that of dorsum of thorax; pubescence of face
dense, largely covering surface, yellowish white in color. Inner orbits slightly
converging below; head very finely and closely punctured, clypeus more finely
so than rest of head; anterior margin of clypeus broadly impunctate with
several irregular strong nodules: area behind ocelli not more closely or
sparsly punctate than rest of head; mandibles not narrowed apically, breadth
at apex of inner tooth equal to breadth near middle. Thorax little if any
more coarsely punctate than head; hind tibial spurs slender and brown.
Punctures of anterior metasomal terga slightly coarser than those of meso-
scutum, separated by about half a puncture width; punctation of posterior
terga progressively finer; sixth metasomal tergum medially truncate, this
region with a projecting dark brownish flange lateral to which are shallow
emarginations separating the truncation from the low, obtuse, rounded, lateral
lobes; seventh tergum obtusely angulate medially, sides straight; second
metasomal sternum large, its margin rounded, neither truncate nor emarginate
but median portion somewhat produced posteriorly, therefore strongly
rounded; third sternum with posterior margin nearly straight except for
large median emargination filled with long yellowish hairs; posterior margin
of fourth sternum broadly rounded.
CALIFORNIA: Gavilan, on Helianthus gracilentus, June 9, 1950
(P. H. Timberlake) [U. C., R.].
JANUARY, 1954] = MICHENER—MEGACHILIDAE Sik
ANTHOCOPA MALLOGNATHA Michener
NeEvapba: Twenty-two miles south of Las Vegas, April 4, 1953,
on composite (J. W. MacSwain, E. G. Linsley) [U. C., B.]; six
miles south of Las Vegas, April 6, 1953 (Ray F. Smith) [U. C., B.].
Anthocopa mirifica Michener, new species
Anthocopa mortua, Michener, 1943, Ann. Ent. Soc. Amer., 36:78 (female,
not male).
The female associated with the male mortua in 1943 proves to
be quite unrelated to moriua, and is here renamed. It is described
in the reference cited above. The most distinctive features of
mirifica are the short clypeal truncation of the female, shorter than
the distance from the end of the truncation to the lateral angle of
the clypeus, and the short, robust, but tridentate mandibles of the
male.
Male: Length 6.6 to 7 mm. Pubescence white, not obscuring surface of
clypeus; inner orbits distinctly converging below; head rather coarsely and
closely punctate, clypeus more finely and more closely so, particularly an-
teriorly; anterior margin of clypeus narrowly impunctuate, truncation rounded
laterally and much longer than distance from end of truncation to lateral
angle of clypeus, medially with broad shallow emargination and median
projecting tooth; mandibles short and robust, not narrowed medially, apices
tridentate, distance from apex of lower tooth to middle tooth greater than
distance from apex of middle tooth to upper tooth. Mesoscutum with punc-
tation little if any coarser than that of vertex; mesepisterna with punctures
similar to those of mesoscutum and genal areas; outer and posterior portions
of tegulae brown; upper portion of enclosure of propodeum roughened.
Metasomal punctation dorsally about as coarse as that of mesoscutum but
punctures more widely separated although in most areas separated by no
more than a puncture width, laterally punctures even coarser than those of
mesoscutum; first five metasomal terga provided with apical bands of white
pubescence; sixth tergum broadly truncate posteriorly with no distinct sub-
lateral angles and without a projecting flange; seventh tergum broadly
rounded posteriorly; second sternum large, posteiror margin distinctly emar-
ginate medially; third sternum broadly emarginate posteriorly, the emargina-
tion completely filled with a very long, yellowish fringe; fourth sternum with
margin slightly produced and rounded medially; genital coxopodite robust
although tapering to slender apex, hairs visible from above short but under
surfaces subapically with rather long hairs.
Since he males associated with mirifica were not collected with
females, they are not designated as types.
Holotype female: MazourKa Canyon, Inyo Mountains, Ivyo
County, Catirornia, May 25, 1937 (N. W. Frazier) [K. U.]. One
female paratype from each of the following localities, all in Catt-
FORNIA: near Darwin Falls, Argus Mountains, Inyo County, May
52 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
30, 1937 (C. D. Michener) [K. U.] ; Westgard Pass, Inyo County,
June 15, 1937, on Encelia farinosa (C. D. Michener) [K. U.]; Box
Canyon, on Chaenactis carphoclinia, April 21, 1952 (P. H. Timber-
lake) [U. C. R.]. Eighteen female paratypes from seven miles west
of Westgard Pass, Inyo County, California, some on Encelia fari-
nosa, June 26, 1953 (J. W. MacSwain, N. Nakakihara, D. D.
Linsdale) [U. C., B.].
Males are from Surprise Canyon, Panamint Mountains, Inyo
County, California, on Chaenactis brachypappa, April 28 and 29,
1953 (P. D. Hurd) [U. C., B.] and (P. H. Timberlake) [U. C., R.].
LITERATURE CITED
MIcHENER, CHARLES D.
1943. The American bees of the genus Anthocopa with notes on Old
World Subgenera (Hymenoptera, Megachilidae), Ann. Ent. Soc.
Amer., 36:49-86.
1939. A revision of the genus Ashmeadiella (Hymen, Megachilidae),
Amer. Midland Nat., 22:1-84.
1949. Records and descriptions of American megachilid bees (Hymen-
optera), Jour. Kansas Ent. Soc., 22:41-59.
CHANGE OF THE SPECIES NAME OF MYZUS LANGEI
ESSIG TO MYZUS CALLANGEI ESSIG
E O. Essic
University of California, Berkeley
The specific name of Myzus langei Essig 1936 is herewith
changed to Myzus callange Essig because it is preoccupied by
Myzus langei Borner 1933. This latter species was first described
in the genus Trilobaphis (Borner 1933). Subsequently in 1952 the
author published the following in nomenclature: “Myzus (Syn.
Trilobaphis and Galobium langet C. B. 1933)” (Borner 1952,
p. 131.)
REFERENCES
Borner, CARL
1933. Kleine Mitteilungen tber Blattlause. Biol. Reichs. Zweigs., Naum-
burg (Saale): p. 4.
1952. Europae centralis Aphides di Blattlause Mitteleuropas Namen,
Synonyme, Wirtspflanzen, Generationszyklen. Weimar Druck-und-
Verlagsanstalt Gebr. Knabe K. G. Weimar. p. 131.
JANUARY, 1954] PHILIP—TABANIDAE Se,
NEW NORTH AMERICAN TABANIDAE (DIPTERA).
PART IV. ZOPHINA NEW GENUS FOR “APATOLESTES”
EISENI TOWNSEND FROM LOWER CALIFORNIA?
CorneEwius B. Puiiip?
Townsend (1895) described “Apatolestes (or nov. gen.) eiseni
n.sp.” from San Jose de Cabo, Lower California, based on a
“wholly blackish’ male specimen with peculiar antennae, and
stated “it is entirely different from ChArysops in its antennal struc-
ture, and can hardly be either a Silvius or an Apatolestes.” He de-
ferred setting up a new genus, however, on the male alone. This
type was destroyed in the 1906 earthquake in San Francisco’, but
J. M. Aldrich had examined it in October 1905, making a rough
drawing of the antennae showing the scape longer than tall, and
noting only in addition in correspondence with J. S. Hine that the
ocelli were large and on a high prominence. Also in correspondence
with Hine on July 6, 1907, Townsend forwarded on unpublished
manuscript he had prepared on “Zophotabanus n. genus” in refer-
ence to this dark fly, based on two additional topotypic males and
a female, the latter, unfortunately, not in good preservation. It
seems doubtful if any of these additional specimens were lost with
the type since Aldrich saw only the type at the California Academy
of Sciences a few months previous to the great fire. None was
indicated as being forwarded with the manuscript to Hine. Among
Townsend material in the British Museum, there remains one
badly pest-damaged male labelled, “San Jose del Cabo, L. Calif.
Sept.” and “Melanophlebys n.gen. eiseni Twns. types” apparently
in Townsend’s own handwriting. This specimen was loaned to the
writer through courtesy of Mr. H. Oldroyd. It seems obvious that
the other pair was destroyed by pests before this was sent to the
British Museum. Heavy reliance must therefore be placed on pub-
lished and unpublished notes to place this species for catalog pur-
poses pending capture of more satisfactory specimens. There is
no greater prospect that additional specimens will turn up in the
near future than have in the previous intervening years, and present
1 From the Federal Security Agency, Public Health Service, National Institutes
of Health, National Microbiological Institute.
2Principal Medical Entomologist, Rocky Mountain Laboratory, Hamilton,
Montana. :
3 Van Dyke (Entomological News, 17(6) :222. 1906) mentioned the types of
Coleoptera, Hemiptera and Hymenoptera as having been saved. E. S. Ross advises
that the Odonata types. then on loan, have been returned and are extant.
54. THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1]
comments are offered to clarify the status of this long-questioned
name. The Hine correspondence has been furnished through gen-
erosity of Mr. Edward S. Thomas of the Ohio State Museum.
In some respects, Townsend’s notes describe specimens related
to Veprius presbiter Rond. of Chile, but the three species of
Veprius all have Tabanus-like antennal plates with dorsal angles,
and the differentiation of eye facets in the males is not marked as
in “A.” eiseni. Furthermore, there are minute, scattering, ocular
hairs in the former, none in what remains of the “A.” eiseni speci-
men; the face is much more sunken between the swollen cheeks in
the latter, while the palpi are as long as the proboscis. If the female
has a denuded subcallus (described as a “transverse callosity” )
and a probable “longitudinal callosity” on the front, considering
other described characters, this species does appear distinct on a
generic level as discussed below. Since it is a pangoniine, a variant
of Townsend’s original manuscript name is adopted here, namely,
Zophina, n. gen. (it is impossible to find an unawkward patronymic
with five genera already named after Townsend). His additional
unpublished notes follow:
“Head very short conical in profile, inore or less flattened in appearance
across the eyes; 2 front about one-half as wide as either eye, narrowed
toward vertex; 2 eyes contiguous for a long distance, from near base of
antennae to ocellar tubercle. Ocelli present. Proboscis short. Eyes bare.
Difference in size of facets in 6 eyes very marked, abrupt, not gradual, the
small facets being limited to less than lower verticle one-third of eye. Front
of 2 with a transverse callosity next base of antennae, divided longitudinally
by a median furrow and defined above (posteriorly) by a deep transverse
furrow. There is probably also a longitudinal callosity between the trans-
verse one and the ocelli, but it is not distinct in this specimen which is
poorly preserved. Face short, antennae springing from a little below the
anterior angle of eyes, Antennae not stout, rather small, more slender in
the $ than in the 9. First joint not elongate, but little if any longer than
wide; second joint hardly one-half as long as first in 2, in 2 appearing but
little shorter than first; third joint composed of five annuli, the basal one
swollen and bead-like in &, less distinctly bead-like in ?, as thick as first
and second antennal joints; remaining annuli abruptly slender in 2, slightly
stouter in 2 and tapering more gradually from basal annulus. Third antennal
joint in 2 but little longer than first and second taken together, in ¢ con-
siderably longer. Hind tibiae with two spurs. Femora and tibiae not thick-
ened, moderately slender in $, a little heavier in 9, the front tibiae of 9
slightly bowed. Wings normal, with none of the posterior cells narrowed or
closed, longer than abdomen. Type, Apatolestes eiseni Towns.
“[“Zophotabanus”] eiseni Towns. Proc, Cal. Acad. Sci. Ser. 2, Vol. Ly
p. 596, No. 9 (Apatolestes or nov. gen.).
JANUARY, 1954] PHILIP—TABANIDAE 55
“San Jose del Cabo. One 2, and two @ &, Sept. These three additional
specimens enable me [Townsend] to properly characterize the form as a
new genus. It is very distinct from the previously known genera. The 9
measures full 10 mm. in length; wing 9 mm. The @, 7 to 8 mm. The whole
insect has a blackish appearance, even including the halters and wings,
though the color of the body and head is dark brownish. The front, face,
and antennae are dilute brownish, more dilute in the 3’s; the tip of
anulate portion of antenna is black.”
Townsend’s failure to publish this manuscript is probably ex-
plained by his statement written to Hine that he intended hence-
forth to concentrate on the higher Diptera.
A dermestid larva (molted skin still present) has destroyed the
entire abdomen, one side of the thorax with one wing missing,
parts of one eye and one antenna of the British Museum specimen.
A little damage along the dorsum of the plate and 3 annuli of the
other antenna has occurred but all segments are present. The fol-
lowing additional but limited description can be made. The basal
plate of the third segment, though “bead-like” in profile, is laterally
compressed and not as thick as the pedicel and scape. The last is
a little longer than thick, not produced above, with sparse black
hairs; pedicel as tall but about two-thirds as long; plate subequal
to the scape in length but more compressed laterally, and the four
terminal annuli nearly twice as long as the plate and constricted
abruptly not tapering from their juncture. The frontal triangle is
restricted due to the extensive eye area, and is bare and shining
brownish, not swollen or much raised above the eye level in profile
in contrast to Veprius. The face to and including the oral margins
unusually depressed somewhat as in A patolestes, the cheeks in con-
Sequence appearing much swollen throughout their length. The
palpi are slender, a little longer than the proboscis, very shaggy
brown-haired almost concealing the apparently attenuated apices,
unlike the truncated condition seen in most Apatolestes. The la-
bellae are small and fleshy. Brief relaxing appeared to revive
Silvius-like, irregular maculations on the undamaged part of the
one eye. The subepaulet of the wing is bare and there is a short
spur present at the fork of R,,;. The legs are all intact, with no
pale hairs and no accentuated hind tibial fringe. The outer fore
tarsal claw is a little longer than the inner.
The specimen is too badly damaged to warrant its establish-
ment as a lectotype. Since the original description was based on
56 THE PAN-PACIFIC ENTOMOLOGIST | VOL. Xxx, NO. 1
the male, a future female could not be used for this purpose though
it will undoubtedly be the better for more accurate, ultimate de-
termination of relationships of this species.
In some respects Z. eiseni is intermediate between Apatolestes
and Silvius. The writer was inclined to place the published species
as a sub-genus under Silviws. Study of this specimen even though
damaged enables corroboration of Townsend’s earlier opinion that
it is distinct on a generic level.
SUMMARY
Zophina new genus is proposed for Apatolestes (?) eisent
Townsend, genotype species from Lower California. Comment is
made on Townsend’s published and unpublished notes on this
species. |
REFERENCE
TownsEnp, C. H. T.
1895. On the Diptera of Baja California, including some species from
adjacent regions. Proceedings of the California Academy of
Sciences, Ser. 2, 4:593-620.
MIROLEPISMA DESERTICOLA SILVESTRI,
A MYRMECOPHILE FROM CALIFORNIA
(Thysanura: Lepismatidae)
Wittram J. Watt Jr.
University of California, Davis
Mirolepisma deserticola was described by Silvestri in 1938 from
a single specimen collected in Tucson, Arizona in 1908. Since that
time, no mention has been made of its biology or of its occurrence
in California. Mallis (1941), however, did mention that he had
observed Thysanura running in and out of the nest of the harvester
ant, Pogonomyrmex barbatus var. nigrescens, near Riverside, Cali-
fornia. He evidently did not collect or attempt to identify the
species of Thysanura.
In 1950 W. F. Barr, now of the University of Idaho, while col-
lecting beetles in the vicinity of Winnemucca, Nevada, found two
female Mirolepisma in the nest of harvester ants. This discovery
led the writer to search the desert areas of California and Nevada
1 All species of ants were identified by M. R. Smith of the United States
National Museum.
JANUARY, 1954] WALL—MYRMECOPHILE 57
for additional material. The locality records of M. deserticola and
the ants' with which it was found are listed below:
POGONOMYRMEX OCCIDENTALIS OCCIDENTALIS (Cresson)
Nevapa: Winnemucca, 26 April 1950 (W. F. Barr), 2 2 Q.
POGONOMYRMEX CALIFORNICUS ESTEBANIUS (Pergande)
CALIFORNIA: 6 mi. W. of Indio, Riverside County, 5 April 1951 (J. W.
MacSwain), 2 64,5 2 9; Palm Springs Station, Riverside County, 20
April 1951 (W. J. Wall, R. C. Bechtel, E. I. Schlinger and E. J. Taylor),
646, 2 2; Sheep Hole Mts. (summit), San Bernardino County, 30 March
1952 (R. C. B. and E. I. S.), 64, 22; Bagdad, San Bernardino County,
80: March 1952- CR. GrB rand Hello.) sods ne 5
PocoONOMYRMEX CALIFORNICUS (Buckley), s. lat.
CALIFORNIA: Whitewater, Riverside County, 28 March 1952 (R. C. B. and
1 aA Bei ah) Aero sara
MyYRMECOCYSTUS SEMIRUFA (Emery)
CALIFORNIA: 6 mi. W. of Indio, Riverside County, 5 April 1951 (J. W.
MacSwain),1 @.
VEROMESSOR PERGANDEI (Mayr)
CALIFORNIA: Palm Springs, Riverside County, 21 April 1951 (W. J. W. and
R. C. B.), 1 4,1 2; Whitewater, Riverside County, 28 March 1952 (R. C. B.
and E. I. S.), 24, 2 23; Bagdad, San Bernardino County, 30 March 1952
(R. C. B. and E. I. S.), 6 @, 2 23; 29 Palms, San Bernardino County, 30
March 1952 (R. C. B. and E. I. S.), @ 6, 2 9; Sheep Hole Mts. (summit),
San Bernardino County, 30 March 1952 (R. C. B. and E. I. S.), 2%, 2 2;
Rand, Kern County, 31 March 1952 (R. C. B. and E. I. S.), @@, 2 2?
SOLENOPSIS sp.
CALIFORNIA: Cabazon, Riverside County, 20 April 1951 (W. J. W. and
kh. C. B.), 1 9°. Magnesia Canyon, Riverside County, 21 April 1951 (W. J. W.
and E. I. S.),1 9.
MIscELLANEOUS RECORDS
CatiForniA: N.W. of Barstow, San Bernardino County, October 1928; Salton
Sea Beach, Imperial County, 22 April 1951 (W. J. W. and R. C. B.), 1 @,-
1 2 (ants not identified) ; 1 mi. S. of Desert Beach, Imperial County, 10
April 1952 (W. H. Lange), 1 Q [with Thermobia domestica (Packard) ].
The species of ants with which Mirolepisma was found are in
general desert forms. According to Creighton (1950) and Mallis
(1941) P. occidentalis, P. californicus, and P. californicus esteban-
ius are found in the desert areas of Arizona and Southern Cali-
fornia. The range of P. occidentalis extends northward into Nevada
and eastward to New Mexico, while P. californicus is also found
in Texas and Mexico.
M. deserticola is well adapted to life in sandy areas. Its legs are
armed with stout spines and when individuals are exposed to the
2 Crickets of the genus Myrmecophila were also found in this nest of ants.
3 Several Reticulitermes hesperus Banks were also present.
58 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
light, they will dig rapidly until completely buried. The exact re-
lationship between the ants and silverfish has not been definitely
established, but it was noted that the Mirolepisma carefully avoided
contact with the ants. This observation led the writer to conclude
that a commesal relationship exists between the two groups.
In order to ascertain the food habits of M. deserticola, a num-
ber of silverfish were taken alive and reared in a controlled
temperature cabinet in the laboratory at Davis. The temperature
employed was 25 degrees C. + 1 and the relative humidity was 75
percent + 3. No water was given directly to the insects; the food
was dry whole wheat flour. Over a period of 14 months, the culture
thrived and hundreds of ova and nymphs were produced from the
original group of some 40 adults.
Since no detrimental results were incurred when the silverfish
were separated from their hosts, it is believed that M. deserticola
ebtains its food from the products stored by the ants rather than
any secretion or regurgitated fluid from the body of the ants.
According to Creighton (1950), Mallis (1941) and Wheeler
(1926), Pogonomyrmex occidentalis, P. californicus, P. californi-
cus estebanius, Veromessor pergandei, and some species of Solen-
opsis are seed collectors. The feeding habits of Myrmecocystus
semirufa appear to be uncertain. Creighton (1950) claims that
repletes are used to store honey, but that the bodies of other insects
are also collected and stored. Mallis (1941) showed that in one
instance in Southern California this species attended aphis, ap-
parently for secretions of honey dew.
REFERENCES
CREIGHTON, W. S.
1950. The ants of North America. Bull. Mus. Comparative Zoology,
104:1-585, 57 pls.
Ma tis, A.
1941. A list of the ants of California with notes on their habits and
distribution. Bull. So. Calif. Acad. Sci., 60(2) :1-44, 3 pls., 25 figs.
SILVESTRI, F.
1938. Due novi Generi Deserticoli di Lepismatidae (Insecta: Thysa-
nura). Boll. Lab. Ent. Agr. Portici, 1:348-353, 3 figs.
WHEELER, W. M.
1926. Ants. Columbia University Press, N. Y., pp. 11, 268, 575.
JANUARY, 1954] WIRTH—INTERTIDAL FLY 29
A NEW INTERTIDAL FLY FROM CALIFORNIA, WITH
NOTES ON THE GENUS NOCTICANACE MALLOCH
(Diptera: Canaceidae)
Witus W. Wirts?
Since the publication of my revision of the family Canaceidae
(Wirth, 1951), I have received some additional material, including
a fine series representing an undescribed species of Nocticanace
Malloch. A description of the new species is presented here, the
status of Nocticanace is clarified, and some new American distribu-
tion records for this genus are added.
Genus Nocticanace Malloch
Nocticanace Malloch, 1933, B. P. Bishop Mus. Bull., 114:4; Wirth, 1951,
Occas. Papers B. P. Bishop Mus., 20:269; Wheeler, 1952, Ent. News,
63:91.
Because Malloch’s paper, as stated in a footnote, was issued
as Pacific Entomological Survey Publication 7 on Febraury 27,
1933, Nocticanace should date from 1933, and not from 1935, the
date when the complete volume of Bulletin 114 was assembled.
Neave’s Nomenclator Zoologicus and the Zoological Record both
erroneously give the date as 1935 and the citation given in my
paper was not clear. Most of this information has been correctly
cited by Wheeler (1952), who is of the opinion that Nocticanace
is very likely the same as Canaceoides Cresson, 1934, in which case
Malloch’s name has priority.
As suggested by Wheeler, the characters separating Canaceoides
and Nocticanace do not seem to be very strong, and the new species
here described brings the two groups closer together. One cannot
very well merge these two genera, however, without considering
also the close ties which I have already pointed out (1951, p. 264)
between Canaceoides and Canace exhibited through Canace mari-
tima Wirth. Until more species are known, I believe it most
practical to retain the narrower generic concepts and in the follow-
ing discussion I will point out a combination of characters suitable
for the differentiation of Canaceoides and Nocticanace. In any
event, the ensuing new combinations will have to be made, in view
of the priority of Nocticanace.
Nocticanace arnaudi Wirth, new species
(Figure 1, a)
Male, female: Body length of male about 3 mm., of female 3.5 mm.;
1 Bureau of Entomology and Plant Quarantine, Agricultural Research Adminis-
tration, U. S. Department of Agriculture.
60 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
wing 3.7 mm. by 1.4 mm. Color opaque black, dorsum black tinged with
brownish; antennae and palpi brownish black: face and cheeks pruinose,
pearly gray when viewed from above, brownish from below; humeri, pleura,
legs and abdomen dark brown, with pruinose gray lights; wings and squamae
opaque brownish with dark veins; haltezes whitish.
Frons broader than long, flat in front over eyes, ocellar prominence
well-developed, brownish in color, with 10-15 fine hairs. Three strong fronto-
orbitals, the intervening hairs long and fine; one pair of strong proclinate
interfrontals; ocellars strong; inner and outer verticals strong; postverticals
absent. Face bare, median carina strong between antennae. Cheeks each with
three strong bristles, the inner one directed mesad, the outer two upcurved,
with a small hair about half as long out of line below the lateral pair by
half the distance between their bases. Third antennal segment slightly
broader than long; arista short pubescent. Palpus with 1-4 apical hairs.
Thorax on each side with four strong dorsocentrals, one strong humeral,
a strong posterior notopleural and an anterior one half as long, one strong
presutural, two strong supra-alars; humeri and anterior margin of mesonotum
except between dorsocentral lines with strong, erect setae, rest of mesonotum
bare. Scutellum with four strong marginals, the disc bare. Mesopleura with
numerous, scattered, long hairs and setae, sternopleura each with a long
fine hair and a few scattered setae. Legs with numerous, stout, curved hairs,
these short except the posteroventral series on fore femora; tarsi with distal
segments markedly flattened.
Abdomen with scattered, long erect hairs. Eighth tergite of female with
two, long, lateral hairs reaching apices of genital lamellae and four or five
fine hairs about half as long between; eighth sternite also with a few long,
fine hairs; dorsal lamellae of opipositor stout, upcurved, each with two stout,
black, apical spines and about three smaller, brownish, preapical ones on
dorsal side. Ninth tergite of male (fig. 1, a) with the ventral processes each
broadly attached at base, ventral margin with numerous fine hairs, apex
prolonged in a slender, straight, fingerlike, external lobe bearing only micro-
scopic setulae; a shorter, broader, inner lobe present on the dorsal margin
of the ventral processes hidden by the subapical, dorsal angle and bearing
humerous, stout, ventromesally projecting spines.
Holotype 3, allotype, Point Lopos, MonTEREY County, CAtt-
FORNIA, February 4, 1948, W. Wirth (on intertidal rocks) (type
No. 61608, U.S.N.M.). Paratypes: 33 3, 499, same data as types
(in U.S.N.M.); 10, Laguna, Orange County, California, August
1, 1932, J. M. Aldrich (U.S.N.M.); 839°, 8 99, beach south of
Pescadero, San Mateo County, California, December 15, 1951, P.
H. Arnaud, Jr. (5 in U.S.N.M., 3 deposited in California Academy
of Sciences, San Francisco, and 8 returned to Mr. Arnaud).
About the only characters by which this species differs from
Canaceoides nudata, the genotype of Canaceoides Cresson, are the
presence of the very fine secondary hair ventrally out of line on the
cheeks rather than a fourth, equally strong and aligned genal
JANUARY, 1954] WIRTH—INTERTIDAL FLY 61
bristle; the dise of the scutellum bare rather than with a pair of
small bristles; the eighth tergite of the female with two long hairs
in the marginal row reaching the apices of the ovipositor lamellae
rather than with a row of small subequal hairs and in the structure
of the male genitalia (compare figure 1, a, with figure 5, c, of
nudata in Wirth, 1951). These are actually the only characters
which can be relied on to separate the genera Nocticanace and
Canaceoides. | believe that for generic separation, emphasis should
be placed on these characters, rather than on the condition of the
anterior notopleural, which is absent in most species of Noctican-
ace, weak in Canaceoides and in N. arnaudi and strong in N.
chilensis (Cresson).
a. arnaudi b. texensis
Figure 1. Male genitalia of Nocticanace, lateral views of ninth tergite.
a, NV. arnaudi, n. sp.; b., N. texensis (Wheeler).
NOcTICANACE CHILENSIS (Cresson), new combination
Canace chilensis Cresson, 1931, Dipt. Patagonia and S. Chile, 6:116.
Canaceoides chilensis, Cresson, 1934, Trans. Amer. Ent. Soc., 60:221; Wirth,
1951, Occas. Papers B. P. Bishop Mus., 20:269.
New record: Panama, Canal Zone, February 10, 1939, C. H.
Richardson, 1¢.
This is the first record of N. chilensis from outside of Chile.
This species belongs in Nocticanace rather than Canaceoides be-
cause of the absence of hairs on the disc of the scutellum, the pre-
sence of two elongate hairs on the eigth tergite of the female
and the presence of small secondary hairs between and below the
long genal bristles. Since there are from three to six strong genals
62 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
in chilensis, I believe that the presence of the smaller, secondary
hairs is a better generic character than the actual number of strong
genals. The presence of two equally strong notopleurals in chilensis
limits the use of this character in generic differentiation.
NocTICANACE TEXENSIS (Wheeler), new combination
(Figure 1, b)
Canaceoides texensis Wheeler, 1952, Ent. News 63:92 (49, Galveston,
Texas. )
New records: Boynton Beach, Palm Beach County, Florida,
August 10, 1951, W. W. Wirth, 8¢' 3’, 8 99; Mona Island, Puerto
Rico, August 6, 1939, L. F. Martorell, 19 (all in U.S.N.M.).
The Florida specimens were collected from a shelf of limestone
rock about a hundred yards long on the Atlantic Ocean beach. This
rock projected from the water only at low tide and was covered
with a scanty growth of filamentous green algae. Through the
kindness of Dr. Wheeler I have compared these specimens with
a female paratype of texensis with which they agree well. The
small, out-of-line, fourth genal, the absence of hairs on the disc
of the scutellum, the absence of the anterior notopleural and the
presence of the pair of long hairs on the eighth tergite of the
female will place this species in Nocticanace rather than Canaceo-
ides. In fact this species is practically indistinguishable from N.
peculiaris Malloch, the genotype of Nocticanace, differing mainly
in that the body is not quite so dark, the palpi are yellowish rather
than brown and the two anterior genal bristles are more closely
approximated and lack the fine seta below and between which is
found in peculiaris. The male genitalia of texensis, which have not
been described, have the ninth tergite (figure 1, b) with the ventral
processes semidetached, each greatly expanded distally into two
setose lobes, the outer or dorsolateral lobe thumblike, bearing
dense, long setae except on the lateral surface; the ventromesal lobe
in the form of a flattened, rounded lamella bearing dense, very
long setae on the inner surface.
LITERATURE CITED
Wuee ter, M. R.
1952. The dipterous family Canaceidae in the United States. Entomo-
logical News, 73:89-94.
Wirtu, W. W.
1951. A revision of the dipterous family Canaceidae. Occasional Papers
B. P. Bishop Museum, 20:245-275.
JANUARY, 1954] MICHENER—BEE PUPAE 63
OBSERVATIONS ON THE PUPAE OF BEES
(Hymenoptera: Apoidea)
CHARLES D. MIcHENER!
In the course of a recent study of bee larvae, pupae of a number
of species have come to hand. The present investigation was under-
taken in order to glean whatever information could be obtained
on the pupal characters and the relationships of groups.
The pupae, as is well known, exhibit essentially the shape and
form of adults, and the general features of pupae have been
described and illustrated by many authors (e.g. Packard, 1897).
From our standpoint the important pupal features are those not
repeated in the adult, since the adult characteristics are well known.
Unfortunately most authors have not systematically recorded these
structures which are peculiar to pupae. As a result, most published
accounts of pupae are of little value from the present standpoint.
Those pupal characters which are peculiar to pupae consist
principally of spines and projections arising from various parts
of the body. Their functions are unknown, although in some cases
it is possible to see hairs of the adult projecting into them in older
pupae. This is by no means always the case, spines being present
(although small) in such relatively hairless bees. as Neopasites.
Nonetheless, the original function of these projections may have
been to provide space for the development of the long hairs char-
acteristic of bees and associated with their pollen collecting habits.
On broad flat areas of the body these hairs can develop in a
recumbent position, but at the ends of segments where the spines
are of most frequent occurence long hairs cannot well develop in
this position. Thus the long spines of the coxae and trochanters
serve to house the long hairs arising on these segments in some
bees (fig. 1). This explanation cannot well account for the scutal
tubercles of Xylocopa or Melecta, for example, but does seem to
be a possible explanation of most of the pupal projections.
It is interesting that certain adult spines and projections which
have arisen repeatedly among the various bee groups correspond
to the pupal projections. For example, anterior coxal spines,
1 Contribution number 807 from the Department of Entomology, University of
Kansas.
Specimens were made available through Dr. J. W. MacSwain of the University
of California and Dr. Bernard Burks of the Division of Insect Identification,
Bureau of Entomology and Plant Quarantine.
64, THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
found in adults of at least certain species of such unrelated genera
as Colletes, Nomada, Megachile, and Xylocopa, but generally ab-
sent in adult bees, are formed inside of pupal spines which are
found in virtually all bees but ordinarily contain only hair. Thus
it would seem that the pupal spines provide a potentiality for the
development of adult spines.
Table I summarizes the characteristics peculiar to pupae of
bees. The characters require explanation as follows:
1. “Scape’—When the antennal scape bears a small median tubercle,
it is marked +.
2. “Vertex”—The symbol + indicates that a pair of tubercles are
present on the vertex more or less in the position of the lateral
ocelli.
3. “Frons’—The symbol ++ indicates the presence of a pair of low
tubercles, one in front of the summit of each eye.
4, “Lateral angles of pronotum”—The symbol -+ indicates that these
angles are produced to spines.
5. “Posterior lobes of pronotum”—The symbol + indicates that these
lobes are produced.
6. “Mesoscutum”—The symbol + indicates that paired tubercles are
present.
7. “Scutellum”’—The symbol ++ indicates a pair of large erect pro-
tuberances while + indicates a pair of smaller, anteriorly directed
ones. (See Melecta, excluded from table since specimens are not
available. )
8. “Metanotum”—The symbol + indicates a median protuberance.
9. “Tegulae”’—The symbol + indicates a protuberance, +-+ a spine,
+ a protuberance present or absent.
10. “Wings”—The symbol + indicates a small median tubercle on each
forewing and usually a small basal tubercle as well.
11-13. “Coxae”—The symbol + indicates an inner apical coxal spine;
+ is used if the spine is unusually long.
14-16. ‘“Trochanters’—The symbol -+ indicates a posterior apical spine;
+t is used if the spine is unusually long.
17-18. “Femora’—The symbol -+ indicates a posterior or inferior basal
protuberance on the femur while ++ indicates a spine in this
position.
19. “Hind tibiae (base)”—The symbol + indicates a protuberance near
the base of each hind tibia, at about the position of the apex of the
basitibial plate, while +--+ indicates a spine in this position.
20. “Hind tibiae (apex)”—The symbol + indicates an outer apical
spine at the apex of the hind tibia.
21. “First tergum spiculate’-—The numerals indicate the anteriormost
metasomal tergum to bear a transverse subapical row of spicules.
Commonly spicules are found from the tergum indicated in this
row back to the fifth (females) or sixth (males) tergum, but
this is not universal.
JANUARY, 1954] MICHENER—BEE PUPAE 65
22. “Size of tergal spicules’—The symbol + indicates minute spicules,
giving rise to setae which are more conspicuous than the spicules;
+ -+ indicates larger spicules, while ++ + indicates very large
spicules.
23. “Long setae’—The symbol + indicates long setas on vertex, mesos-
cutum, and metasomal terga.
Nomadopsis
Lasioglossum
Neopasites
Megachile
Diadasia
Anthophora
| Tizone
ieee a
Policana
Halictus
Xylocopa
5. Posterior lobes of pronotum
iw)
Rea
‘6. Mesoscutum
7. Scutellum
Peele ie Oy ie
8. Metanotum
9. Tegulae
=)
0. Wings
_
1. Fore coxae
—
2. Mid coxae
eee ea tale dere ee
bape le aia
es
be
Bats
ee
oe
a
fy)
=)
3. Hind coxae
epepel TT
ae
Pat
eg
a
ed
bee
eS
a
pr
—_
4. Fore trochanters
—
5. Mid trochanters
6. Hind trochanters
—_
17. Fore femora
18. Mid femora
9. Hind tibiae (base)
20. Hind tibiae’ (apex)
21. First tergum spiculate
—_
Blea sede
pee
22. Size of tergal spicules
Is eee ee Re epee
Fa
Pes
Bae
elk
Soe Pas ee cree ee ae
Fe eee a ee ee eae
Po ie aes eae
Si
i
EB
a
Ee
Be
i)
ele
f
Be
e
Shieh eee
+ {+]4+]4+]4]4]4
ae es ee
It is evident from a study of Table I that, so far as the few
23. Long setae
bee pupae available are concerned, considerable support for exist-
ing classifications (see Michener, 1944) is provided. Thus the
66 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
family Colletidae is distinguishable by the absence of tergal
spicules, a character shared only with Apis. The family Halictidae
is recognizable by the numerous and very strong protuberances,
the tubercles on the wings and the spine or tubercle at the base of
the hind tibiae being found only in this family. Nomia falls clearly
with the Halictidae on the basis of pupal characters, although some
authors have put it with the Andrenidae. Megachile differs from
all other known bee pupae in the presence of long setae. It is
interesting that megachilid larvae are the principal bee larvae hav-
ing setose bodies. The larger anthophorine bees (Emphor, Diad-
asia, Anthophora, Melecta) are distinguished from the Apinae by
the presence of mesoscutal tubercles, and in this respect they
resemble Xylocopa.
Fig. 1. Fore leg of Anthophora linsleyi Timberlake, pupa, showing by |
broken lines the developing aduli leg within and by dotted lines some of the
hairs inside the pupal spines.
The following descriptive comments are limited to those fea-
tures of the pupa not shared by adults. For example, inner apical
spines of the tibiae are not mentioned since the tibial spurs of the
adults form inside of them and their position and number is re-
JANUARY, 1954) MICHENER—BEE PUPAE 67
flected by the adult structures. Spines and other projections are
absent unless stated to be present.
COLLETES FULGIDUS Swenk
Lateral angles of pronotum and posterior lobes of pronotum
produced; mesoscutellum with a pair of large protuberances;
metanotum with large median protuberance; coxae, trochanters,
and bases of anterior femora with long spines.
Montara, California, September, 1940 (J. W. MacSwain).
POLICANA HERBSTI Friese
As described for Colletes but vertex with distinct pair of tu-
bercles (in positions of lateral ocelli) ; lateral angles of pronotum
not produced; tegulae produced; posterior margins of metasomal
terga swollen.
Correo Nunoa, Chile (Claude—Joseph).
NOMADOPSIS EUPHORBIAE (Cockerell ) |
Mesoscutum with pair of very small tubercles, one on either
side of midline, in front of middle; coxae and trochanters with
spines; bases of fore femora each with inferior projection; meta-
somal terga, beginning with the second, with subapical rows of
spicules, the rows interrupted medially.
Riverside County, California, August 17, 1946 (J. W. MacSwain).
AUGOCHLORA PURA (Say)
Vertex with pair of protuberances (in positions of lateral
ocelli) and pair of lower ones just in front of upper ends of eyes;
antennal scapes each with small protuberance; scutellum with pair
of high protuberances; metanotum with median broad protuber-
ance; middle of each forewing with protuberance; smaller one at
base of each wing; coxae and trochanters each with small spine;
bases of fore femora each with protuberance; base of hind tibia
with short spine; metasomal terga with large subapical spicules,
only a few on first tergum and these unusually large.
_ Short Mountain, Shenandoah, Virginia, June 6, 1941, in rotten log
(A. B. Gurney).
LasiocLossum (CHLORALICTUS) SPARSUM (Robertson)
As Augochlora pura but pair of protuberances in front of upper
ends of eyes and on antennal scapes absent; tegulae somewhat
protuberant.
Lawrence, Kansas, June 24, 1951 (C. D. Michener).
LasiocLossum (EvyLArus) Kincarpit (Cockerell) '
As Augochlora pura but small protuberances on antennal scapes
absent; spicules of first metasomal tergum like those of second.
Montara, California, June 12, 1940 (J. W. MacSwain).
68 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
HALICTUS TRIPARTITUS Cockerell
As in Augochlora pura but pair of protuberances in front of
upper ends of eyes and on antennal scapes absent; tegulae some-
what protuberant; basal spine of each rear tibia a mere protuber-
ance but apex of rear tibia with long spine on outer side (in ad-
dition to usual tibial spurs on inner side) ; spicules of first tergum
similar to those of second.
Chino, Arizona, July 4, 1950 (J. G. Rozen, R. H. Beamer).
NoMIA MELANDRI Cockerell
Vertex with pair of small tubercles (in positions of lateral
ocelli) ; scutellum with pair of high tubercles; metanotum with
median projection; tegulae each with sharp spine; forewing with
weak median and basal projection; coxae and trochanters with
spines, those of former rather short, especially on rear coxae; fore
and middle femora with protuberances at bases; base of hind tibia
with spine; metasomal tergum three and following with subapical
spicules.
Delta, Utah, June 27, 1950 (G. E. Bohart, C. D. Michener).
MEGACHILE (CHELOSTOMOIDES) sp.?
Coxae and trochanters with spines; metasomal sterna produced
apically (female) ; vertex and median region of mesoscutum with
long setae; metasomal terga two and following with subapical rows
of long setae.
Blythe, California, April 2, 1941, in old Colletes burrow (E. G. Linsley,
J. W. MacSwain).
MecAcHILE (LITOMEGACHILE) BREVIS Say
As in the species of Chelostomoides but vertex with three small
tubercles representing positions of ocelli.
Lawrence, Kansas (C. D. Michener).
XYLOCOPA VIRGINICA (Linnaeus)
Mesoscutum with a pair of tubercles in front of middle, one
on each side of midline; coxae and trochanters with long spines;
metasomal terga two and following with small subapical tubercles;
last tergum produced to a hard spine.
Veitch, Virginia, July 7, 1914 (T. E. Snyder).
NEOPASITES sp. ?
Coxae and trochanters with small spines; metasomal terga two
and following with subapical rows of spicules.
The specimen is in poor condition and there may be more pupal
structures than indicated.
JANUARY, 1954] MICHENER—BEE PUPAE 69
Lawrence, Kansas, April 5, 1951, froin nest of Calliopsis andreniformis
Smith (C. D. Michener).
EMPHOR BOMBIFORMIS (Cresson )
Mesoscutum with two pairs of tubercles, the anterior pair in
front of middle, the posterior pair behind middle, the latter closer
together than the former; scutellum swollen; coxae and trochanters
with spines, anterior femora each with basal projection; metasomal
terga two and following with subapical spicules.
Hattiesburg, Mississippi, August 20, 1944 (C. D. Michener).
DIADASIA ENEVATA (Cresson)
Posterior lobes of pronotum produced; mesoscutum with a pair
of tubercules behind middle; scutellum with two tubercles, large
and directed forward; coxae and trochanters with spines, those of
rear trochanters short; anterior femora each with spine at base;
metasomal terga two and following with subapical rows of spicules.
Delta, Utah, June 27, 1950 (G. E. Bohart, C. D. Michener).
ANTHOPHORA LINSLEYI Timberlake
Posterior lobes of pronotum produced to spines; mesoscutum
with a pair of tubercules behind middle; scutellum with a pair
of anteriorly directed tubercles; coxae and trochanters each with
a spine; bases of fore and middle femora each with a long spine;
metasomal terga two and following with subapical rows of spicules.
Twenty miles east of Bakersfield, California, March 29, 1941 (E. G.
Linsley, J. W. MacSwain).
ANTHOPHORA (CLISODON) FURCATA SYRINGAE (Cockerell)
As above, but no long spine at base of middle femur.
Mineral King, Tulare County, California, August 10, 1939 (G. E. Bohart).
MELECTA spp.
Semichon (1922) has described the pupa of Melecta armata
Panzer. It is said to be similar to that of its host, Anthophora
personata Erickson, except that the pair of mesoscutal tubercles are
erect, each forming a multidentate crest, and the scutellar tubercles
are much larger and directed posteriorly to form spines. The
mesoscutal tubercles are shown to be similarly modified in Melecta
miranda Fox by Porter (1951).
BoMBUS AMERICANORUM (Fabricius)
Coxae and trochanters with apical spines; metasomal terga two
and following each with subapical row of short setae.
Lawrence, Kansas, August, 1950 (C. D. Michener).
BoMBUS VOSNESENSKII Radoszkowski
Agrees with B. americanorum.
fo
ae ba.
we.
70 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
Hat Creek, Lassen County, California, June 4, 1941 (E. G. Linsley,
C. D. Michener).
TRIGONA CUPIRA Smith
Coxae and trochanters with spines, those of fore and hind
coxae very short; fore and middle femora each with projection at
base; metasomal terga two and following with subapical rows of
setae.
Juan Mina, Canal Zone, May 4, 1945 (C. D. Michener).
APIS MELLIFERA Linnaeus
Coxae and trochanters with spines, those of front coxae short,
of front trochanters unusually long; fore femora each with a spine
at base, middle femora with a blunt projection, hind femora with
a broad rounded projection.
Lawrence, Kansas, June 1, 1952 (M. H. Michener).
BIBLIOGRAPHY
MICHENER, CHARLES D.
1944. Comparative external morphology, phylogeny, and a classification
of the bees (Hymenoptera). Bull. Amer. Mus. Nat. Hist., vol. 82,
pp. 151-326.
Pacxarp, A. S.
1897. Notes on the transformations of higher hymenoptera. II and III,
; Jour. New York Ent. Soc., vol. 5, pp. 77-87, 109-120.
Porter, JOHN C.
1951. Notes on the digger-bee, Anthophora occidentalis, and its in-
quilines. Iowa State College Jour. Sci., vol. 26, pp. 23-30.
SemicHon, Louis
1922. Sur la nymphe de Melecta armata Panzer (Hym. Apidae). Bull.
Soc. Ent. France, p. 192-194.
A NEW SPECIES OF DOBSONFLY FROM CALIFORNIA
(Megaloptera: Corydalidae)
Donatp E. Mappux
Chico State College, Chico, California
During a recent investigation, a number of immature forms of
some dobsonflies of the genus Protochauliodes were reared, and a
new species was noted. It is most closely related to Protochauliodes
minimus (Davis) but differs noticeably in the structure of the
terminalia.
Protochauliodes aridus Maddux, n.sp.
Male: General body color closely resembling that of Protochauliodes
minimus. Head triangular, widest across eyes, tapering ‘caudad to its nar-
JANUARY, 1954] MADDUX—DOBSON FLY 71
rowest width at point of attachment to thorax; tuft of long hairs on lateral
border of head, just posterior to each eye. Antennae dark brown, simple,
filiform, approximately the same length as the body; antennal segments twice
as long as broad and bearing short bristles closely appressed to the margin
of the segments to which they are attached. Mouthparts rufous, apex of
distal point of incisor of mandible usually not extending below proximal end
of mandible. Prothorax longer than wide, the sides nearly parallel, meso-
thorax and metathorax broader than long. Wings hyaline and cinerous, with
a conspicuous, transverse, fuscous blotch surrounding the medio-cubital
cross-vein; other such blotches are scattered over the wing surfaces, especially
in the costal and subcostal cells of the fore wings. Blotches fewer on the
hind wing and confined almost entirely to an area along the costal margin.
Hind wing with a small, round, fuscous mark, just proximad to each of the
two inner radio-medial cross-veins. Fore wing slightly longer than the hind
wing, but both essentially alike in venation, the venation agreeing with that
of other members of the genus and being very much the same as that of
Protochauliodes minimus. Aedeagus wide at base, narrowing to half the
width at the apex; apex notched. Base of gonopod with dorso-medial side
enlarged into a conspicuous tuberosity. Apex of gonopod half the height of
the base. Body length 16 mm.; alar expanse 57 mm.
Female: Much larger than male. Body length 21 mm.; alar expanse
82 mm. Antennae approximately the length of the body; antennal segments
rectangular, lightly pilose.
Holotype, male, reared by the author from a larva taken in a
dry stream bed near the Neal Road, seven miles southeast of Cuico,
Butte County, CatrrorniaA, May 15, 1951. The allotype was
reared from a larva taken at the same locality, May 10, 1951. Two
paratypes were reared from larvae collected at the same locality,
one on May 8, 1951, the other on May 9, 1951; both are males.
Holotype and allotype are in the museum of the California Aca-
demy of Sciences, San Francisco. Paratypes are in the collection
at Chico State College.
The larval and pupal forms from which the above specimens
were reared were taken in streams which have water for only a
few days in the winter. They were found under rocks in cells
fashioned to prevent the drying of the specimen. Eggs were collected
in the field and were also obtained from specimens reared in the
laboratory. The egg masses are rectangular in outline; the eggs
are arranged in a series of parallel rows, about 3,000 in a large
bunch. The micropylar ends all face in the same direction. The eggs
are deposited in June, hatch in about a week, and the very small
larvae burrow into the dry soil near the larger rocks. Pupation
occurs in March, April, and May. The adults hatch in May and
June.
72 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
A REDESCRIBED SPECIES AND A NEW GENUS AND
SPECIES OF THE FAMILY LEPISMATIDAE IN CALIFORNIA
(Thysanura )
WituaMm J. WaLt Jr.
University of California, Davis
Very little information is available on the species of this family
in California. In 1896 a new species (Lepisma rubro-violacea) from
Mexico, Arizona and California, was described by Schott. He failed
to realize the importance of certain structures and did not include
these in his description. However, his figures were excellent and
accurately identified this species. The specimens examined by Schott
were evidently lost in the San Francisco earthquake and fire of
1906, and no mention of this form has appeared in the literature
since 1905. ;
In 1950, W. F. Barr of the University of California, collected
one specimen from the desert near Borego Valley. Since this time,
numerous specimens have been found in the Colorado Desert
beneath stones, boards and cardboard cartons.
CTENOLEPISMA RUBRO-VIOLACEA (Schott)
Lepisma rubro-violacea (Schott, 1896. Proc. Calif. Acad. Sci., (2)6:190-192,
pl. 18, figs. 45-51.
Ctenolepisma rubro-violacea Escherich, 1905. Zoologica, orig.-ab. 18 (heft 43)
95-96, fig. 39. |
Redescription. Female. Length: body 10.2.mm.; antenna 10.4 mm.; cercus
10mm.; median caudal filament 11.20 mm.; ovipositor as seen from below,
projecting 2 mm. from segment IX. Width: at eyes 1.6 mm.; mesothorax 2.8
mm.; Xth abdominal segment 1.6 mm.; ovipositor .2 mm. Body elongate,
tapering gradually posteriorly.
Head color reddish particularly the frontal and lateral areas; thorax
white with exception of prothoracic acrotergite which has strong reddish
pigmentation reaching almost to center; abdomen reddish with inverted “v
shaped” white areas; pigmentation becoming darker towards posterior. Scales
of dorsum reddish brown with white scales surrounding each setal tuft on
thorax and abdomen; ventral scales white; setae of entire body golden; legs
white, pigmented with red; setal tufts on head prominent.
Labial palpus four segmented, pigmented with red; distal segment
hatchet shaped with five sensory papillae arranged in a single row along
anterior margin; maxillary palpus five segmented, pigmented with red.
Prothoracic sternite with five pair of setal tufts; mesothoracic sternites
with two pair of setal tufts; metathoracic sternite with one pair of setal tufts.
Tergite X widely triangular and weakly rounded at tip, wider than long.
Outer dorsal setal combs (lateral) on abdominal tergites J-VIII; abdominal
tergites II-VII with 3+-3 setal combs (i.e. one lateral, one subdorsal and one
JANUARY, 1954] WALL—THYSANURA 08
dorsal) ; tergite I with 1++-1 (2 inner pair lacking); tergite VIII with 242
(central pair lacking) ; IX with none; X with 1+1. Only one pair of setal
combs on ventral sternites III through VII. Three pairs of reddish pigmented
styli present on gonocoxites VII, VIII and IX, posterior pair longest. Cerci
and median caudal filament reddish alternating with white, annulated;
antennae same.
Male: similar to female except for differences in genitalia; gonocoxites of
segment IX long and narrow in female, short and stout in male.
Discussion. C. rubro-violacea and C. lineata (Fabricius) are
very similar in appearance when the scales are removed. However,
the clypeus of C. lineata is strongly pigmented on the lateral aspect
where the setal tufts are located and in the center; in C. rubro-
violacea the pigmentation is faint or lacking. Also the lateral aspect
of the area around the setal tufts of the labrum may be faintly pig-
mented in C. lineata and not in C. rubro-violacea. Further, the
prothoracic acrotergite is pigmented only on the lateral aspects
in C. lineata, while on C. rubro-violacea, the pigmentation extends
throughout except for a thin median band.
The number of setal tufts on each side of the prosternal plate
in C. rubro-violacea may vary from 4 to 5. The remaining char-
acteristics appear to be constant.
The description of the neotype female given above was made
from a single specimen now preserved in alcohol. However, the
concept of this species is based on 8 females and 11 males which
were studied alive by the writer and later in alcohol. Some of the
original members of this series were dissected and used for study
of the internal anatomy and in part have been mounted on slides
in the possession of the writer. The remaining complete specimens,
consisting of the neotype 2 and 5 neoparatypes (2¢' ob and 3 99)
have been deposited at the California Academy of Sciences, San
Francisco, California.
Distribution. Schott gave the following localities: Sierra La-
guna, San Jose del Cabo, Baja California; Guaymas and San
Miguel de Horcasitas, Sonora Mexico; Tucson, Arizona (coll. B.
Eisen). In addition, he stated that this species is “richly represented
in California collections and seems to be very common.”
Neotype locality. CALIFORNIA: CABAZON, RIVERSIDE Co.
Material examined. Borego Junction, San Diego Co., 9 April
1950 (W. F. Barr) ; Cabazon, Riverside Co.; 20 April 1951 (W. J.
Wall, R. C. Bechtel, E. I. Schlinger and E. J. Taylor) ; Salton Sea
Beach, Imperial Co., 21 April 1951 (W. J. W. and R. C. B.) ; 2 mi.
74, THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
E. of “The Narrows”, San Diego Co., 23 April 1951 (R. C. B.);
Whitewater, Riverside Co., 28 March 1952 (R. C. B. and E. I. S.).
While collecting in the Colorado Desert near Cathedral City,
the writer and E. I. Schlinger of the University of California dis-
covered a new thysanuran beneath a large stone. Several other
specimens were later taken at other localities and in two instances
with C. rubro-violacea. The favored habitat of this new species
appears to be beneath stones, boards and other places of con-
cealment in desert areas.
Leucolepisma new genus
(Figures 1—9)
Description. Body elongate, slender, thorax wider than abdomen tapering
weakly posteriorly. Head with numerous setal tufts, those arranged postero-
mesad and anterio-mesad to the antennae, are large and very obvious;
thoracic nota broad, each bearing a pair of setal combs on the postero-dorsal
margin; lateral margins with setal tufts and individual setae; legs long,
tarsal claws very long, claws of prothoracic leg at least one and one third
times the second tarsal segment; three pair of dorsal abdominal setal combs
on tergites II-VII; lateral setal combs on several sternites and one pair of
median setal combs on several segments; ovipositor short, stout and tip
armed with short, stout blunt spines.
Type of the genus: Leucolepisma arenaria Wall, new species.
This genus is similar in general to Thermobia but differs in
having three rows of dorsal setal combs on the lateral aspect of
the abdominal tergites, instead of two; by the length of the tarsal
claws, and by the short ovipositor terminating in short blunt spines.
Leucolepisma arenaria new species
(Figures 1-9)
Female. Length: body 8.16 mm.; antenna 11.60 mm.; cercus 8.16 mm.;
median caudal filament 9.60 mm.; ovipositor as seen from below not extend-
ing beyond gonocoxites of segment IX. Width: at eyes 1.44 mm.; mesothorax
2.25 mm.; Xth abdominal segment 1.22 mm. Head and body color white;
dorsal surface with brown and yellowish white scales forming a distinct
pattern; scales of head brown; those of the thorax with alternating irregular
cross bands of brown and yellowish white; those of abdomen with alternating
patches of brown and yellowish white on each segment; when freshly molted,
much darker; ventral surface with white scales; setal tufts of head golden.
Legs white with light reddish setae and faint reddish pigmentation on tibia
and lst tarsal segment; cercus and median caudal filament reddish with
light segments at intervals; antenna same.
Setal tufs of head prominent. Labial palpus four segmented, distal seg-
ment hatchet shaped, shorter than the penultimate one and bearing five large
JANUARY, 1954] WALL—THYSANURA 75
EXPLANATION OF FIGURES
Leucolepisma arenaria, n.g., n.sp. Fig. 1 Abdominal tergite X. Fig. 2. Pro-
thoracic sternite. Fig. 3. Mesothoracic sternite. Fig. 4. Metathoracic sternite.
Fig. 5. Terminus of outer ovipositor valve showing digging spines. Fig. 6.
Labium. Fig. 7. Left mandible. Fig. 8. Right maxilla. Fig. 9. Right prothoracic
leg (note length of tarsal claws).
76 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
sensory papillae arranged in a single row along anterior margin; number of
setae on inner edge of the lacinia varying from four to six; maxillary palpus
six segmented.
Prothoracic sternal plate with three pair of setal tufts; mesothoracic
sternal plate with one pair setal tufts; metathoracic sternal plate with one
pair of setal tufts.
Tergite X, with tip narrowed, rounded, wider than long. Outer dorsal
setal combs on abdominal tergites J-VIII; abdominal tergites II-VII with 3+-3
setal combs (i.e. three on lateral aspect of each tergite); tergite I with
1-++1 [2 dorsal (inner) pair lacking]; tergite VIII with 242 (subdorsal pair
lacking) ; IX with none; X with 1+-1. One pair of sublateral ventral setal
combs on sternites IV-VIII and a single median row on sternites III-VII.
Styli present on gonocoxites of segments VIII and IX; those on IX longer;
ovipositor short and stout not extending beyond gonocoxites of sternite IX.
Male: like the female, except for differences in genitalia and while the
gonocoxites of female are long and narrow, those of male are short and broad.
Holotype: SALTON SEA Beacu, ImpeEriaL Co., CaLirornia, 22
April, 1951 (W. J. Wall and R. C. Bechtel).
Material examined. California: Magnesia Canyon, Riverside
Co., 21 April 1951 (W. J. Wall and E. I. Schlinger) ; Borego
Junction, San Diego Co., 22 April 1951 (W. J. W.) ; Borego Valley,
San Diego Co., 22 April 1951 (W. J. W. and E. J. Taylor) ; 10 mi.
W. of Truckhaven, San Diego Co., 11 April 1952 (W. H. Lange).
Discussion, The only variations of the characters described
above are as follows: the number of setal tufts on the lateral mar-
gins of the prothoracic sternite may vary from two to four, and
faint pink pigmentation may be present or absent on the thoracic
nota.
The description of the holotype was made from a single speci-
men now preserved in alcohol. However, the writer’s concept of
this genus and species is based on 5 99 and 9 o'o' which were
studied alive and later in alcohol. Some of the original members
of the type series were dissected and used for study of the internal
anatomy and in part are mounted on slides in the possession of the
writer. The remaining complete specimens consisting of the holo-
type 2 and 40’ ob paratypes have been deposited at the California
Academy of Sciences, San Francisco, California.
Escuericu, K. REFERENCES
1905. Das System der Lepismatiden. Zoologica, orig. (Stuttgart), ab.
18 (heft 43) :95-96, fig. 39.
ScHort, H.
1896. North American Apterygogenea. Proc. Calif. Acad. Sci., 6(2):
190-192, pl. 18. figs. 45-51.
JANUARY, 1954] PACIFIC. COAST ENT. SOC. it,
PACIFIC COAST ENTOMOLOGICAL SOCIETY
J. Gorpon Epwarps J. W. MacSwain D. D. JeEnsEN
Vice-President President Secretary
PROCEEDINGS
Two Hundred and Twenty-eighth Meeting
The two hundred and twenty-eighth meeting of the Pacific Coast En-
tomological Society was held at 2:00 p. m. on Saturday, January 31, 1953,
in the Morrison Auditorium of the California Academy of Sciences, San
Francisco. President MacSwain conducted the meeting. The following mem-
bers were present: G. F. Ferris. R. Matsuda, J. W. Tilden, Laura M. Henry,
Paul Bartholomew, Paul Arnaud, J. P. Harville, Lorin Gillogly, J. G. Edwards,
P. D. Hurd, Jr., J. D. Lattin, C. Don MacNeill, W. C. Bentinck, W. V. Garner,
E. O. Essig, A. E. Michelbacher, W. W. Middlekauff, W. D. Murray, E. S.
Ross, K. F. Innes, J. W. Green, R. F. Smith, E. G. Linsley, C. E. Kaufeldt,
J. W. MacSwain, D. G. Denning, H. B. Leech, W. C. Day, R. L. Usinger,
and D. D. Jensen. The following visitors were present: Jacob Bergamin, Mir
Mulla, S. Abul Nasr, Mostafa Hafez, J. W. Chapman, J. Nelson, Mrs. John
Nelson, Mrs. Lorin Gillogly, Alan Gillogly, James Gillogly, Barbara Hovanitz,
Wm. Hovanitz, Joseph E. Ryus, Joan Linsley, and Mrs. Leslie H. Burman.
The minutes of the meeting held December 6, 1952, were read and
approved.
Mr. John O. Stivers was elected to membership in the Society.
In response to President MacSwain’s call for notes and exhibits, Dr. Ross
exhibited a California tarantula collected by Dr. F. X. Williams near Mt.
Diablo. The spider had been stung by a Pepsis wasp about July, 1952, and
was still alive at the time of the exhibit although paralyzed. When first
received, the spider could scarcely move its appendages. At this date the
paralysis had considerably reduced and the spider could almost walk again.
It is very doubtful that the spider could recover sufficiently to secure food
and survive.
Professor Ferris displayed a pre-publication copy of Dr. Cook’s “Ants
of California.”
Dr. MacSwain reported that the Society’s gavel had been used at a
number of historic meetings of the national entomological societies last
December in Philadelphia. Dr. Linsley had requested the use of the gavel
and reported that it had been used at the last meeting of the Entomological
Society of America, the joint executive committee meeting of the Entomo-
logical Society and the American Association of Economic Entomologists,
and finally it was used at the first meeting of the first governing board of the
new Entomological Society of America, following the amalgamation of the
two societies.
Dr. MacSwain showed photographs of cells of two species of andrenid
bees which had been parasitized by anthophorid bees. These anthophorid
78 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 1
bees, belonging to the genera Nomada and Holonomada, apparently lay two
eggs in each cell they parasitize. Thus when several parasitic bees have
visited the same cell, four or even as many as six eggs are to be found
inserted into the walls of the cell. The first parasitic larva to hatch imme-
diately searches out the other eggs and destroys them with its well developed
mandibles. This larva does not feed on the eggs it destroys but after crushing
them searches out the egg of the host bee and consumes it. Later the pollen
and nectar mass stored by the Andrena is eaten by the parasite. It would
appear that this multiple oviposition by the parasite has two principal
advantages to the species. In the first place, the parasite’s egg must hatch
well ahead of that of the host bee. Thus by placing two eggs in each cell,
the parasitic species insures extreme selection for a minimum incubation
period. The second advantage would be to insure the production of a parasite
in the event of the destruction of one egg by some other agent.
Dr. MacSwain introduced Dr. John Smart, Lecturer in Zoology, Univer-
sity of Cambridge, who spoke on the subject “Wicken Fen, Cambridgeshire,
A British Nature Reserv2.” Dr. Smart’s discussion, which was supplemented
by pictures, is summarized below.
One of the oldest nature reserves created by private effort in the United
Kingdom is that at Wicken Fen, Cambridgeshire. It is a small reserve when
measured against the national parks and other reserves of the North American
continent, being only a little more than one square mile in area. To some
extent the land has been modified by the operations of man but not nearly
to the extent that has the surrounding countryside which has been drained
and modified by intensive agriculture.
Wicken Fen has been relatively little interfered with and it represents
the condition in which the whole of “Fenland” existed in medieval times
before drainage and other improvements were carried out. “Fenland” is a
large area extending roughly from Lincoln to Suffolk and from Huntingdon
to King’s Lynn. It is a shallow basin with very poor water drainage, and
in olden days was one vast marsh with, here and there, small areas of
raised land called “islands” upon which there were such human settlements
as existed. One of the most typical of these “islands” is the Isle of Ely with
its well-known cathedral.
The whole area is apparently slowly sinking; robably the whole of the
North Sea area was at one time covered with “fen”. On the higher land
there were forests of oaks but as the land sank these trees were killed and
marsh plants multiplied in the fresh water that accumulated and formed the
vast marshes. Gradually the marshes filled up with peat and the oak trees,
now called “bog oak,” were preserved under the peat.
The peat is 16 to 18 feet thick. The greatest draining activity took place
in the 17th century, when great areas were drained and prepared for agricul-
ture which is now intensive over nearly the whole of Fenland. Wicken Fen,
with on or two other even smaller areas, are all that is left of the medieval
“Fenland.” Their importance from the conservancy point of view is that they
are the sole surviving samples of what this medieval fen-flora and fen-fauna
were like and their possible interest when considered as survivors of the
even more extensive fens of the pre-historic period.
JANUARY, 1954] PACIFIC COAST ENT. SOC. 79
Wickn Fen requires considerable management. It is in the last stages of
the formation of dry land from peat-bog and is largely covered with sedge
(Cladium). If left completely to itself it would become covered with bushes
and possibly at a later stage with trees. The objective in its management is
the maintenance of the conditions of the wet sedge-fen which is the flora
association that follows that of reeds (Phragmites), which require a certain
depth of water over the peat and that precedes that of the bushes which,
with the moor grass (Molinia), requires the plant’s base, but not the root
system, to be clear of the permanent water table.
Wicken Fen is probably best known as one of the homes of the rare
British Swallow-tail Butterfly (Papilio machaon brittanicus Seitz), and of
the experimental attempts to replace the Large Copper Butterfly (Lyceanea
dispar dispar Haworth), which became extinct, with the Dutch race of this
butterfly (Lyceanea dispar batavus Oberth.). Collecting of the first named is
carefully restricted; unfortunately the colony of the latter died out during
the last war.
Dr. Smart’s address resulted in a discussion which included consideration
of nature reserves in the San Francisco Bay region. Dr. Ross, who raised this
point, suggested that some of the Antioch sand dune area would be desirable
to conserve. Following Dr. Usinger’s proposal that the Society take the
initiative in the matter, President MacSwain appointed Dr. Usinger and
Dr. Hurd as a committee to investigate the feasibility of the idea.
At the close of the discussion the meeting was adjourned.—D. D. JENSEN,
Secretary.
Two Hundred and Twenty-ninth Meeting
The two hundred and twenty-ninth meeting of the Pacific Coast En-
tomological Society was held at 2:00 p. m. on Saturday, March 7, 1953, in
the Morrison Auditorium of the Califurnia Academy of Sciences, San Fran-
cisco. President MacSwain conducted the meeting. The following members
were present: J. W. MacSwain, Owen Bryant, E. S. Ross, L. R. Gillogly,
P. S. Bartholomew, Wm. Hazeltine, Victor Stombler, H. B. Leech, A. E.
Pritchard, R. D. Morgan, D. D. Linsdale, Gordon Marsh, W. V. Garner,
J. D. Lattin, T. F. Leigh, K. S. Hagen, J. J. Drea, W. C. Day, R. L. Usinger,
K. F. Innes, Jr., C. E. Kaufeldt, C. W. Hildebrand, J. R. Helfer, J. G.
Edwards, D. P. Furman, B. F. Augustson, L. A. Wood, Jr., H. H. Keifer,
E. L. Kessel, E. O. Essig, J. W. Tilden, Benjamin Keh, John O. Stivers, and
D. D. Jensen. Visitors were present as follows: Mrs. Lorin R. Gillogly, James
J. Gillogly, Alan R. Gillogly, N. D. Walker, Gerald Kraft, Mir Mulla, Mrs.
Carl Miescke, Carl Miescke, Don Burdick, Albert Alberts, Lois May Bastian,
James W. Chapman, Lloyd A. Andres, Robert L. Langston, Kenneth M.
Fender, Edmond O. Loomis, Albert Rudnick, and S. McAgley.
The minutes of the meeting held January 31, 1953 were read and
approved.
Donald J. Burdick was elected to membership in the Society.
President MacSwain appointed Dr. Middlekauff and Dr. Tilden to fill
the vacancies in the Membership Committee and Mr. Paul Arnaud to the
Program Committee.
80 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
By a unanimous vot2 of the members present, Dr. Usinger was author-
ized to serve as the official representative of the Society at the 14th Inter-
national Congress of Zoology to be held at Copenhagen, Denmark, August
5-12, 1953.
In response to the President’s call for notes and exhibits, Dr. Furman
displayed an adult female of Otobius megnini, the spinose ear tick, as an
example of potential longevity of the species when held under laboratory
conditions. This specimen was taken as a nymph on December 16, 1949, from
a human host. The normal hosts are sheep and other ruminants. After being
held in a pill box for over three years until March 6, 1953, the specimen
was found to have moulted. The resulting adult female is active and only
partially depleted of food reserve.
Dr. Tilden announced that the Lepidoptera Society would hold its
annual meeting in Los Angeles, July 2—5, 1953.
Dr. MacSwain pointed out that the very mild winter, followed by a long
period of no rain, had permitted colonies of the common yellowjacket,
Vespula pennsylvanica (Saussure), to survive the winter. Several strong
colonies have been noted around Berkeley in February although this ground-
nesting species is normally represented by overwintering queens.
Dr. Tilden remarked that Diabrotica undecimpunctata Mannerheim
adults had been active «ll winter in the vicinity of San Jose until within
the last two or three weeks when the coldest weather had occurred.
Mr. Hazeltine exhibited one male of Pleocoma lucia Linsley and three
males of P. nitida Linsley. Notes on the flight habits and distribution were
shown with the specimens in the hope of obtaining additional specimens with
exact data.
Mr. H. B. Leech showed part of the comb from a 4-comb nest of yellow-
jacket wasps, Vespula sp. (probably arenaria Fab.), taken from a tree in
Mill Valley, Marin Co., Calif., in early September, 1952. During September
end October 60 Sphecophaga burra Cresson emerged, and pupal cells of
zbout as many more were present; the species is a widely distributed primary
parasite of Vespula. Also obtained during the same period were 5 adults of
a scavengering lepidopteran, the dried fruit moth (Vitula serratilineella
Ragonot, det. E. G. Munroe) and 52 of its primary parasites, a species of
Braconidae. A single tiny anthocorid bug emerged; it appears to differ from
any in the Academy collection.
Dr. Edwards circulated a copy of the new book on Insect Physiology,
edited by Rader of Tufts College.
Dr. Usinger displayed some of the plates, illustrating California water
bugs, which had been drawn by Arthur Smith of the British Museum. The
excellence of his figures indicates that he is one of the finest illustrators
of insects living in the world today.
President MacSwain then introduced the main speakers of the day.
Professor A. E. Pritchard, of the University of California, Berkeley, spoke
first on “A Review of the Biology of Mites.” He was followed by Mr. C.
Donald Grant, San Mateo County Mosquito Abatement District, who dis-
cussed “Some Morphological Differences between Insects and Mites.”
JANUARY, 1954] PACIFIC COAST ENT. SOC. 81
An abstract of Mr. Grant’s paper follows:
The divergencies between insects and mites began as far back as the
early Cambrian Period when the Chclicerata arose from the Trilobite-like
ancestors of the Insecta. The subsequent evolution of these lines has per-
mitted only the most rudimentary homologies to persist, while the gross
modifications of form have rendered even these somewhat obscure. Convergent
evolution has yielded many similarities of form between existing representa-
tivs of these groups, but brings their homologous relationships no closer.
The relatively few specialists working with the Acarina and the paucity
of representative material collected, afford only a meager understanding of
the comparative morphology of mites in comparison with the level attained
in the insects. The work with mites is further complicated by their probable
polyphyletic origin, i.e., affinities to the Opilionids and Solpugids.
An initial step in comparing the morphology of mites and insects lies in
determining their corresponding segmental relationships, especially with
regard to head and mouthparts. Snodgrass, in 1948, published a comprehen-
sive paper on arachnid mouthparts, indicating their common relationships
end attempting to overcome the confusion resulting from multiple termin-
ology. If one disregards Snodgrass’ assignments as to segmental constitution,
it is found that the basic constituents of the arachnid mouthparts and legs
conform admirably with the first nine segments of the insect body as recently
brought forth in papers by Ferris and Henry (1948). Substantiating evidence
as to the arrangement of homologous segments in the mites will demand
further studies of the nervous system and musculature therein. Diagrammatic
orientation and terminology of the mouthparts of a typical mesostimgatic
mite were shown in projected illustrations, as were also variations in the
morphology of the body, respiratory orifices, and appendages of certain mites.
Following a discussion, the meeting was adjourned.—D. D. JENSEN,
Secretary.
Two Hundred and Thirtieth Meeting
The two hundred and thirtieth meeting of the Pacific Coast Entomologi-
cal Society was held at 7:30 p. m. on April 11, 1953, in the Morrison Audi-
torium of the California Academy of Sciences, San Francisco. President
MacSwain conducted the meeting. The following members were present:
J. G. Edwards, Alice Gray, E. G. Linsley, P. A. Adams, G. F. Ferris, J. W.
Tilden, Victor Stombler, Laura M. Henry, A. E. Pritchard, P. H. Arnaud,
G. F. Augustson, E. L. Kessel, W. C. Day, Harry Chandler, L. R. Gillogly,
W. W. Sampson, H. B. Leech, J. D. Lattin, E. E. Gilbert, Wm. V. Garner,
Owen Bryant, Thomas Lauret, W. B. Murray, D. G. Denning. R. F. Smith,
P. D. Hurd, Jr., Roy Snelling, K. F. Innes, Jr., E. S. Ross, J. W. Green,
Benjamin Keh, R. C. Miller, J. W. MacSwain, and D. D. Jensen. Visitors
were present as follows: Mary H. Swezey, Otto H. Swezey, Mrs. G. F. August-
son, Alan R. Gillogly, Mrs. L. R. Gillogly, Jim Gillogly, Mrs. O. Bryant,
Robert Langston, Dwight W. Pierce, and James W. Chapman.
The minutes of the meeting held March 7, 1953, were read and approved.
Dr. R. F. Smith, chairman of the program committee, announced that
the annual field meeting would be held May 3, 1953, at Russelman Park,
Contra Costa County.
82 THE PAN-PACIFIC ENTOMOLOGIST | VOL. xxx, NO. 1
In response to the president’s call for notes and exhibits, Dr. Hurd
reported on the collecting results of the Hurd-Smith study of the genera
Diabrotica and Pepsis in Mexico, sponsored by the Associates in Tropical
Biogeography, University of California. He stated that the collecting expedi-
tion of the 1953 dry season in Mexico centered its field activities largely
in the states of Chiapas and Oaxaca. He exhibited material of these genera
which helps to demonstrate that a number of species formerly known to
occur in northern South America range northward well into southern Mexico.
In addition, he displayed the cells of the Anthophorid bee, Melitoma, and
the results of preliminary rearing which included a number of parasites and
inquilines and an apparently new species of Mantispid. This bee was found
nesting in the state of Chiapas, Mexico.
Dr. Pritchard reported that a new family of prostigmatic mites had been
discovered on cockroaches in the eastern United States. This is a remarkable
finding in that, in many respects, the new family is a connecting link between
several families of predacious mites and several families of plant feeding
mites.
Dr. R. F. Smith called attention to the fact that the summer meetings
of the Pacific Slope Branch of the Entomological Society of America would
be held at Lake Tahoe in June.
Dr. Linsley displayed specimens of Glaresis ecostata Fall (Scarabaeidae)
which has been a very rare species. The present collection is of unsual interest
because the beetles wer taken in large numbers coming to light many of
them covered with mud. They were collected at a camp on the Mojave River
at Cronese, San Bernardino County, California, April 3, 1953, by Dr. Linsley,
Dr. MacSwain and Dr. R. F. Smith.
Dr. MacSwain extended a special welcome to Dr. and Mrs. Otto H.
Swezey who, since 1904, have been engaged in enomological work in the
Pacific Ocean area and in particular in the Hawaiian Islands where Dr.
Swezey was entomologist for the Hawaiian Sugar Planters’ Association
Experiment Station.
Dr. MacSwain then introduced Dr. W. Dwight Pierce, Curator of En-
tomology (Retired), Los Angeles County Museum, who spoke on the subject
“How Insects Become Fossils.” Dr. Pierce’s address, which was illustrated
with colored slides, is summarized below.
The palaeoentomologist must think ecologically to properly understand
the insect deposits he studies. The forces which have contributed most to
our records are: the waves, winds, and sands of the sea shore; the sands and
dusts of arid countries; Jand slides; glaciers and river floods, swamps, and
marshes; volcanic lava and dust, and hot mineral waters; asphalt seeps
and bogs; and the resins dripping from trees.
On the seashore many insect fragments are washed in and may find
lodgement in piles of kelp and later be buried in the sands. Most shales are
laid down by sedimentation in water, and many of the fine insect fossils are
in shales. Mud deposits often contain insects, and soft muds and silts often
take the imprints of arthropods. Sometimes these prints are permanently
set and become fossil records.
While volcanic lava is too hot to preserve insects, it may conserve those
JANUARY, 1954] PACIFIC COAST ENT. SOC. 83
underlying it. Volcanic ash deposits preserve the species they bury. Much of
the fossil wood of America was the result of volcanic explosions, and dust
covering. The workings of insects in wood are presrved in the fossils, although
crystallization may change the appearance.
Volcanic hot waters in mineral wells kill many insects, and if highly
mineralized will crystallize upon the insects. At Hot Mineral Spring, north
of the Salton Sea, many insects are being preserved. This is the first step
toward formation of onyx marble.
At Bonner Quarry, Kaibab National Forest, Arizona, onyx marble formed
in the crevices in faulted Permian rock has been found to contain very
primitive earth dwelling insects.
Petroleum deposits at Carpinteria, Sulphur Mountain, McKittrick, and
Ios Angeles are preserving multitudes of insects. Those at McKittrick are
stratified at the rate of 25 years to the inch, and the deposits go back to
Middle Pleistocene. Many water insects are found in all of these petroleum
deposits because, from above, the tar probably looks like water.
The glaciers of the Pleistocene period laid down layers of peat and
lignite in which many fine insects have been preserved, especially at North
Vancouver, British Columbia, and in Pennsylvania. The coal deposits of the
world are millions of years older and contain many fine specimens of ancient
insects.
The resins of trees of long ago and the resins of today are responsible
for the preservation in perfect shape cf many insects.
Following a discussion of Dr. Pierce’s paper, the meeting was adjourned.
—D. D. Jensen, Secretary.
Two Hundred and Thirty-first Meeting
The annual field meeting of the Pacific Coast Entomological Society was
held at Russelman Park, Contra Costa County, May 3, 1953.
The recorded attendance of 66 persons included 21 members and 45
visitors. Members were present as follows: D. D. Jensen, J. W. MacSwain,
P. S. Bartholomew, L. R. Gillogly, P. H. Arnaud. R. Matsuda, Roy Snelling,
W. W. Middlekauff, E. O. Essig, J. G. Edwards, J. W. Tilden, H. F. Madsen,
R F. Smith, E. S. Ross, E. G. Linsley, Owen Bryant, H. B. Leech, W. C. Day,
A. E. Michelbacher, W. H. Lange, and Don Burdick. The following visitors
were present: G. W. Bane, Doris F. Jensen, Diana, Anita, Patricia and Carol
Jensen, Mrs. Lorin R. Gillogly, Allan and James Gillogly, Mrs. John Mac-
Swain,Tinker and Nancy MacSwain, Mrs. Marguerite Arnaud, Mrs. Charlotte
Snelling, Marie Essig, Martha Michelbacher, Phyllis Middlekauff, Jeffrey and
David Middlekauff, Alice Edwards, Jane Ann Edwards, Hazel Tilden, Jimmy
and Bruce Tilden, Catherine Madsen, Carol, Bobby and Kenny Madsen, Libby
Smith, Kathy, Tommy and Donald Smith, Mrs. E. S. Ross, Martha and Clark
Ross, Jim Linsley, Juanita Linsley, Joan Linsley, Lucy Bryant, Thomas Leech,
Mary Leech, Helen L. Day, Pauline S. Lange, Marilyn, Diana and Becky
Lange, and Harry S. Creegor.
Since the park was not open to the public in 1953 the Society had ex-
clusive use of the facilities. The weather was ideal for outdoor activities
which included a spirited game of softball, volleyball, and collecting, both
84 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
aquatic and terrestrial. The group included 25 children who thoroughly
enjoyed the sports and exploring the area around the pond and stream.—
D. D. JENSEN, Secretary.
Two Hundred and Thirty-second Meeting
The two hundred and thirty-second meeting of the Pacific Coast Ento-
mological Society was held at 7:30 p. m. on Friday, October 30, 1953, in the
Morrison Auditorium of the California Academy of Sciences, San Francisco.
President MacSwain in the chair. The following members were present:
A. E. Michelbacher, E. O. Essig, W. W. Middlekauff, E. S. Ross, P. A. Adams,
G. A. Marsh, W. C. Day, P. H. Arnaud. G. F. Ferris, R. L. Usinger, W. Harry
Lange, K. F. Innes, J. W. Tilden, L. M. Henry, Victor Stombler, J. G. Edwards,
Thomas Lauret, H. B. Leech, J. D. Lattin, W. V. Garner, H. L. Hansen, Don
Burdick, J. O. Stivers, P. A. Harvey, R. F. Smith, E. G. Linsley, D. D. Jensen,
Glen M. Cagley, Jane MacSwain, J. W. MacSwain, Gerald Kraft, Joseph
Kamp, George Reichart. The following visitors were present: Dr. and Mrs.
Otto H. Swezey, Mrs. W. C. Day, Carlc Gemignoni, March Pitman, Leta Rae
Lauret, Vincent D. Roth, Joseph E. Ryus, Stephen W. Hitchcock, Libby Smith,
Juanita Linsley and Mrs. George Reichart.
The minutes of the meetings held April 11 and May 3, 1953, were read
and approved.
The following were elected to membership in the Society: Joseph W.
Kamp, Gerald F. Kraft, George B. Reichart, Glen M. Cagley, Mrs. J. W
MacSwain, Professor W. J. Chamberlin, and Hirohiko Nagase, Kanagawa
Pref., Japan.
President MacSwain appointed Dr. Usinger, Dr. Tilden and Dr. Ross
to serve as a nominating committee to propose a slate of officers, at the next
meeting, to serve during 1954.
President MacSwain discussed amendments to the By-Laws of the
Society which have been approved by the Executive Board and stated that
the proposed changes in wording would be mimeographed for distribution
at the next meeting.
Before calling for notes and exhibits, President MacSwain announced
that the speaker for the evening, Dr. P. D. Hurd, who was to have spoken
about the insect fauna of Point Barrow, Alaska, was ill and unable to attend
the meeting.
Dr. Tilden reported the collection of six species of Lepidoptera, two
Diptera and a beetle which were of special interest. Philotes rita B. McD.,
cnce thought to be very rare, is now known to be common in association
with Eriogonum wrightii and related plants. The insects seldom go more
than a few feet from the plants. The larvae feed on the flower heads, and the
adults visit the flowers.
Hesperia uncas lasus Edw. Described from southern Arizona. Known
collections are few. In the grasslands between Prescott and Mingus Mt., about
75 adults were collected in about two hours between thunder-showers in
August, 1953. Most of them were females.
Three species of butterflies have been added to the well-collected Santa
Clara County area in the last two years. Philotes enoptes was found on flowers
JANUARY, 1954] PACIFIC COAST ENT. SOC. 85
of Eriogonum wrightii in September, 1953. Two males of Erynnis lacustra
Wright were found near the summit of Mt. Hamilton. A few individuals of
Strymon auretorum Bdy. were found in Arroyo Bayo. The larva feeds on
Blue Oak, Quercus douglasii.
Mitoura nelsoni muiri Hy. Edw. has been shown to be the Coast Range
subspecies of this species. The food plant seems to be Libocedrus decurrens,
incense cedar.
Cuterebra sp., a rodent bot, has been taken several times in Arizona.
The adults are attracted to water which is strange, since the adults have
atrophied mouthparts. Larvaevorid or tachinid flies, of several species and in
considerable numbers, were found attracted to the flowers of Cliff Rose,
Cowania sp., in Oak Creek Canyon, Arizona.
Moneilema gigas Lec. (Coleoptera). A single specimen was taken in
Wickenburg, Arizona.
Mr. Lattin reported that on a trip last summer with Dr. Usinger and
Mrs. Lattin an interesting collection had been made at Hot Creek, Mono
County, California. At the edge of the hot pools, under rocks and other
debris, nymphs and adults were collected of a new species of Cryptostemma,
of the hemipterous family Cryptostemmatidae. These small (1-2 mm. in
length), active bugs should be looked for in similar habitats throughout
California and other western states. Specimens of the closely allied genus
Ceratocombus, have turned up in Berlese samples of leaf litter from southern
California to the north coastal area. As in Cryptostemma the adults are small,
brown and very active. While these bugs are known to be predacious, their
distribution is poorly known due to their small size and their specialized
habitat. Further collecting will greatly clarify the systematics of this group.
Gordon Marsh presented notes on soil inhabiting organisms which he
and R. O. Schuster have collected from soil and litter in Berlese funnels. The
first samples were taken during January, 1953. Considerable stress was placed
on the accumulation of pselaphids, and in particular the genus Pselaptrichus.
Thus far seven new species have been found in this genus. Samples have been
taken from Santa Cruz, Alameda, Contra Costa, Marin, Sonoma, Mendocino,
Humboldt and Del Norte Counties and from portions of the Sierra Nevada
and Panamint Mountains.
It is of interest that Protura have been found throughout the year rather
than only during the moist fall and winter months. A large number of Protura,
identified by Dr. MacSwain as Eosentomon pallidum, were taken at Fresh-
water, Humboldt County, California. The only previous record from the state
was from a peach orchard at Yuba City. This species represents one of the
most archaic groups because it has spiracles.
An interesting sidelight of this study is the discovery of a number of
species of Coleoptera in which there has been a total loss of functional eyes.
These occur in the families Carabidae, Staphylinidae, Scydamaenidae, Sil-
phidae, Lathridiidae and Curculionidae.
Mr. Leech reported a gift to the Society of $15.00 from F. C. Hottes. He
also reported the collection of Stator limbatus (Horn) (Bruchidae) at Clear
Lake, California. This species was described from Lower California and
86 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 1
Sonora, Mexico. It is recorded from Texas, Arizona and southern California.
There are no specimens in the California Academy of Sciences Collection from
farther north than Santa Monica, Los Angeles County, California.
Adults were taken in numbers at Lucerne, on the east side of Clear Lake,
Lake County, on August 29, 1953 by Mr. and Mrs. Leech. They were on the
flower heads of coxcomb (Celosia argentea var. cristata), but were presum-
ably coming from leguminous trees nearby, since our Santa Monica specimens
were reared from the seeds of Acacia cultriformis. The beetles were identified
by L. J. Bottimer.
Dr. Lange reviewed the 1953 outbreak of the rice leaf miner, Hydrellia
griseola var. scapularis Loew in California. From 10 to 20 per cent of the
rice crops was destroyed. by this insect, resulting in a loss of approximately
$16,000,000. In addition $1,200,000 were spent for insecticide control of the
pest. He discussed its life history, and suggested that future outbreaks might
be prevented by proper crop management, particularly that of water level
in the rice fields.
Dr. Edwards exhibited adults, larvae and eggs of Amphizoa (Amphi-
zoidae). The eggs are extremely large and the ocelli of the larvae are visible
through the egg-coat. The larvae are doubled up but when they emerge from
the eggs are about 3144 mm. long as the first instar of beetles which are only
about 12 mm. long as adults. It was most interesting that the young larva
looks just like the later instars, because the only closely related genus known
is Pelobius (Pelobiidae), whose first instar larva is said to be “nauplius”—
like larva similar to those of Crustacea.
Dr. Otto H. Swezey reported a remarkable instance of polyembryony
which he had recorded this season. His observations follow: “From February
to May of this year an occasional cutworm caterpillar of the species Lycan-
dades purpurea crispa Harv. was found in garden work and weed pulling
at my new home on Fleming Avenue, at the base of the foothills east of San
Jose, California. A few moths were reared, but one full-grown caterpillar
which was found under a board on March 28 failed to pupate, apparently
remaining dormant through the summer months, in the soil of the small jar
in which it was held for observation. Finally, on September 15, this jar was
found to be swarming with chalcid parasites. Being a rather strange situation,
these parasites were killed and carefully counted, with a total of 1051, and
probably a few were missed. .
“The empty dry skin of the caterpillar was examined and found to be
perforated with numerous tiny holes where the adult parasites had issued.
This furnishes a remarkable record of polyembryony.
“The moth which is host in this case was kindly determined by Dr. J. W.
Tilden of San Jose State College. The species of the parasite yet remains
undetermined.”
Dr. Jensen reported three recent developments of interest in the field
of plant virus transmission by insects and mites. Roger M. Drake, Deputy
Agricultural Commissioner of San Luis Obispo County, recently reported that
ithe aster yellows virus had caused a loss of from 10 to 50 per cent (average
30%) of the two and one-half million dollar celery crop in the Arroyo
Grande Valley in 1953. In 1952 the loss also ranged from 10 to 50 per cent
JANUARY, 1954] PACIFIC COAST ENT. SOC. 87
and in 1951 from 2 to 30 per cent.
Black (Phytopathology 43:466) maintained two strains of potato yellow
dwarf virus in plants without insect transmission for 12 and 16 years. When
iested with 454 leafhoppers, the virus had lost its transmissibility by these
insects, whereas 433 control insects produced 102 infections with fresh isolates
of the virus from the field. Dr. Black believes the property of transmissibility
by specific vectors was lost through mutation during the years the virus strains
were kept in plants without insect transmission.
Dr. Slykhuis (Phytopath. 43:484) announces that the eriophyid. mite
Aceria tulipae Keifer, is the vector of wheat streak mosaic virus in South
Dakota. This is only the second plant virus shown to be transmitted by mites.
Dr. Usinger displayed Dr. Ross’ new book “Insects Close Up” and
commented on the wide publicity and favorable reception being accorded
the work.
Dr. Ross reported the recent purchase, by the California Academy of
Sciences, of the Howard M. Parshley collection of Heteroptera, consisting of
26,000 mounted specimens most of which are named. Dr. Ross brought the
collection from Northampton, Mass., to California by car and en route
continued his project of color photography of living insects. Some of his
recent pictures were projected on the screen.
Paul H. Arnaud also showed slides of a collecting trip taken into the
Sierra San Pedro Martir Mountains of Baja California.
During the last portion of the meeting Dr. Usinger commented briefly
cn his recent trip to Europe and on the Fourteenth International Congress
cf Zoology held at Copenhagen. He showed a series of his pictures which
had been selected primarily to show a number of the scientific museums of
Europe and some of the people who were at the Congress or at the museums.
The meeting was adjourned at 9:30 p. m.—D. D. JENSEN, Secretary.
Two Hundred and Thirty-third Meeting
The two hundred and thirty-third meeting of the Pacific Coast Ento-
mological Society was held at 2:00 p. m. on Saturday, November 28, 1953,
in the Morrison Auditorium of the California Academy of Sciences, San
Francisco. President MacSwain conducted the meeting. The following mem-
bers were present: W. C. Day, H. B. Leech, W. R. Kellen, E. O. Essig,
A. E. Michelbacher, L. R. Gillogly, W. V. Garner, K. S. Hagen, J. J. Drea,
E. E. Gilbert, P. H. Timberlake, H. P. Chandler, W. H. Lange, E. G. Linsley,
V. Stombler, P. H. Arnaud, E. S. Ross, J. W. Tilden, J. G. Edwards, G. Kraft,
B. Keh, E. L. Kessel, G. M. Cagley, G. F. Ferris, R L. Usinger, C. E. Kaufeldt,
P. S. Bartholomew, J. W. Green, B. Brookman, R. F. Smith, D. D. Jensen,
J W. MacSwain, J. E. Swift, and E. C. Loomis. Visitors were present as
follows: Jim Gillogly, Mrs. L. R. Gillogly, Allan Gillogly, Lloyd H. Shinners,
Joan Linsley, James W. Chapman, Hazel Tilden, John C. Downey, William
Hovanitz, Bruce Eldridge, B. F. Sargent, Vince Roth, and Pauline S. Lange.
The minutes of the meeting held October 30, 1953, were read and
approved,
The following were elected to full membership in the Society: Miss
Hilary Hacker, Tom S. Briggs, William Anthony Doalin, John Charles Dow-
88 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
ney, John E. Swift and Edmond C. Loomis. William R. Kellen was elected
to student membership.
President MacSwain called for the reports ordinarily given at the annual
meeting of the Society. In the absence of Dr. Miller, the treasurer’s report
was not available.
Mr. Leech announced that, because of the pressure of other work, it was
necessary for him to resign as co-editor of the Pan-Pacific Entomologist.
A motion, made by Dr. Usinger, was passed expressing the appreciation of
the Society for the excellent service Mr. Leech rendered during his tenure
as editor.
President MacSwain briefly explained the proposed amendments to the
By-Laws of the Society which had been mimeographed and were distributed
to the members at the beginning of the meeting. A motion was made, seconded
and passed that the By-Laws of the Society be amended as follows:
AMENDMENTS TO THE BY-LAWS OF THE PACIFIC
COAST ENTOMOLOGICAL SOCIETY
November 28, 1953
PRESENT WORDING
Article IV, Section 4: . . . The treasurer
who is hereby granted authority to ex-
pend the money necessary to send out
notices of meetings and to defray ex-
penses, send out bills, etc., in conjunc-
tion with publication of the Pan-Pacific
Entomologist.
Article V, Section 2, paragraph 2: The
Publication Committee shall appoint an
editorial board for the Pan-Pacific Ento-
mologist consisting of an editor (or edi-
tors) and such associate and assistant
editors and advisory members as may be
deemed necessary.
Article V, Section 4, last sentence: It
shall further be the duty of the commit-
tee to consider members’ applications for
associate and student status and to re-
view the membership from time to time
for persons to be nominated as Honored
members.
Article VI, Section 3: The annual dues
shall be $3.00 for regular members, $2.00
for associate and subscribing members.
PROPOSED WORDING
.... Lhe treasurer who is hereby granted
authority to expend the money necessary
to send out notices of meetings and to
defray expenses, send out bills, etc., in
connection with publications of the So-
ciety and such other necessary expenses
of the Society as are approved by the
Executive Board.
The Publication Committee shall appoint
editorial boards for the Pan-Pacific En-
tomological and other Society publica-
tions, consisting of an editor (or editors)
and such associate and assistant editors
and advisory members as may be deemed
necessary.
Delete: “‘associate and”
The annual dues shall be $5.00 for regu-
lar members, $4.00 for subscribing mem-
JANUARY, 1954] PACIFIC COAST ENT. SOC. 89
Article VI, Section 4: Any member may
become a life member by the payment of
$50 in one sum and shall thenceforth be
freed from payment of annual dues.
Article VI, Section 5: Any regular mem-
ber who lives at such a distance from the
place of meeting that attendance is not
practicable may, upon request, be made
an associate member. The dues for asso-
ciate members shall be $2 per year.
Associate members may resume regular
status by payment of the regular $3 dues.
Article VI, Section 8: All members ex-
cept for student members or as herein
otherwise provided shall receive the pub-
lications of the Society with no addi-
tional charge.
Any member may become a life member
by the payment of $75 in one sum and
shall thenceforth be freed from payment
of annual dues
Delete entire section
Replace with: Members who are in good
standing, and who have retired from ac-
live service may, on request, be con-
tinued as active members without pay-
ment of dues. Moreover, such members,
if they desire, may receive the Pan-Pa-
cific Entomologist upon payment of $1
per year.
All members, except for student mem-
bers, retired members or as herein other-
wise provided shall receive the Pan-
Pacific Entomologist with no additional
charge.
Upon a motion made by Dr. Usinger, Dr. Otto H. Swezey was made a
Retired Member of the Society. Dr. Swezey thus becomes the first to receive
this special type of membership for retired entomologists just created by the
above amendments to the By-Laws.
In response to the President’s call for notes and exhibits, Professor Essig
reported that in August, 1953, he had attended the Rocky Mountain Ento-
mological Conference held at Pingree Park, Colorado. This three-day con-
ference, held annually in recent years, was attended by approximately 150
people. Many of the entomologists in attendance brought their families with
them because the program provides for hiking and social activities as well
es for relatively informal entomological meetings.
Mr. Paul Allen reported that Trogoderma granarium Everts, a dermestid
of oriental origin, was found recently in wheat and barley stored at Angiola
and Alpaugh in Tulare County. The infestation at Alpaugh was very heavy.
The larvae tend to congregate on top of the grain and at the sides of the bins.
It is probable that other grains are also good food for this beetle. A
survey of other warehouses has disclosed an infestation of several years’
standing in Fresno. This had been quite thoroughly cleaned up, but probably
was the source of the other two known infestations in California. Under
favorable conditions there may be several generations a year, but under
unfavorable conditions the larvae may survive two years. The survey is
continuing.
Dr. Linsley was asked by Mr. Allen to comment on the discovery of this
pest in California because the original collection and determination of the
beetles had been handled by the University of California. Dr. Linsley reported
that the insects were first sent in by the Tulare County Farm Advisor’s
Office in October, 1953, to J. E. Swift, Extension Entomologist. They were
examined by Dr. Linsley who recognized the beetles as belonging to the
genus Trogoderma and vepresenting 4 species not common to this area and
90 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 1
possibly an important pest. Dr. Linsley suggested the beetles be immediately
sent to Dr. Beal of Denver, Coloradc, who has recently re-worked all the
speeies of this genus. Dr. Beal determined the beetles as Trogoderma
granarium Everts. He notified Mr. Swift, who in turn immediately informed
Mr. Armitage, Chief of the State Bureau of Entomology.
Dr. Usinger exhibited specimens of Aradus evermanni Van Duzee
(Aradidae) and reported that during the summer field course, Entomology
49, entomology students of the University of California collected specimens
found resting on tent canvas at their camp on White Mountain. This species
is rare in collections and scattered in its recorded distribution. Described
from San Francisco, it has since been found elsewhere in California and in
Arizona and Texas. It was not recorded by Linsley and Usinger in dispersal
flights at Mt. Lassen (Pan-Pacific Ent. 18:84, 1942) or Yosemite (Pan-Pacific
Ent. 20:111, 1944). |
Aradus evermanni belongs to the Lugubris Group (Parshley, 1921), all
members of which are usually found in flight or resting on walls, tents,
screens, etc. The precise habitat is not known for any of these species
including the common Holarctic Aradus lugubris Fallen. The occurrence of
A. evermanni at 10,000 feet on White Mountain in July is interesting because
the only coniferous trees in the vicinity were Pinus flexilis James and Pinus
aristata Engelm.
Dr. Linsley exhibited a series of bees and their parasites that had been
collected in Southern Mexico. The principal bee species was an anthophorid
of the genus Melitoma which digs its burrows in cliffs; while the other bee
species borrow the old burrows of Melitoma. The most unusual of the parasites
in this collection was a series of an apparently undescribed species of
Mantispid reared from the cells of the Melitoma sp.
Mr. Leech passed around the June, 1953, copy of a Japanese entomologi-
cal journal, Shin Konshu. in which there is an obituary, with portrait by
Y. Nishio, of the late Dr. E. C. Van Dyke (vol. 6, No. 6, p. 8).
Mr. Leech exhibited a piece of balsa wood which had formed the pinning
bottom of a cigar box, in constant usc at the Academy for at least the past
two years. On November 21, dust seeping out of it was investigated, and a
series of dead adults and one live larva of a cassenine weevil were found.
The beetles are unlike any from North America, and are presumably of
notropical origin.
Mr. Leech also exhibited a box of beetles, showing the remarkable
resemblances of various Tenebrionidac to species of ten other families.
Dr. Ross projected a number of color slides showing alkali bees of the
genus Nomia in Utah, where they are important in the pollination of alfalfa,
end their bombiliid parasites.
President MacSwain called on Dr. Usinger, chairman of the nominating
committee, to present the slate of officers proposed by the committee for 1954.
There were no nominations from the floor, and the following were elected:
5. Gordon Edwards, President; W. C. Day, Vice-President; D. D. Jensen,
Secretary; R. C. Miller, Treasurer; and W. H. Lange, Member at Large.
Dr. MacSwain then requested President-elect Edwards to assume the
JANUARY, 1954] PACIFIC COAST ENT. SOC. 91
chairmanship of the meeting. Dr. Edwards then called on Dr. MacSwain to
give his retiring presidential address cntitled “Some problems in larval and
adult classifications of the Meloidae.”
Dr. MacSwain pointed out that students of larvae and adults commonly
disagree on the levels of classification to be applied to various groups within
any one family and not infrequently tend to ignore the results presented
from the other viewpoint. The Meloidue are no exception in this regard, and
at the present time, two very different classifications are being used. The
adult classification admits two subfamilies and nine tribes, while most larval
classifications would separate the Meloidae first into two families, and sec-
ondly would divide the major family into four subfamilies and ten tribes.
He then discussed the habits of the adults and larvae which correlate
with these two classifications and showed how, partially on the basis of new
evidence, a single usable classification could be derived. Following the ad-
dress, the meeting was adjourned.—D. D. Jensen, Secretary.
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Vol. XXX APRIL, 1954 No. 2
THE
PAN-PACIFIC ENTOMOLOGIST
CONTENTS
CHAPMAN—Swarming of ants on western United States mountain
SUITING Sas Chau Sa accinhe seve Seamer ten eT ae ee ge eee see pero! 5)
EVANS—tThe male of Tastiotenia festiva._........-------------c---ceeececeneeccnenneneneeeees 103
CHANDLER—Four new species of dobsonflies from California............-....... 105
HOREN—Modified flag for tick collectin g.._.-..-.-..-...se-cecececseeeceeerneeeeeeeneereees 2
MALKIN—Range extension of Notonecta shootei..........--....-.-eceeseceeseeeerenees 112
TODD—New species of Nerthra from California... eceescecteeeseseonoreeneotees 113
HELFER—A new Hippomelas from Califormia i... eeee-seeeceeeeeeoeeeenens 117
FURMAN—A new species of Androlaelaps from Perognathus in southern
(Wali Ronee S cctke et RES «oe ies on, Mere A oe tn Aen ES ee a 119
SNELLING—tThe host of Myrmosula rutilans (Blake) 020... ow.eeeseeseneneee- 124
CHANDLER—New genera and species of Elmidae (Coleoptera) from
GEN DE Eck 1 geen oe So eV ee med Cee RL eed eb Sg EE 125
FENDER—On’ some: Malthodesy.s.,.2 eco ccscscecsepeme pans sos cee Varsha ent eles eee ro teevemnese 131
TIMBERLAKE—Two new species of Nomada, subgenus Gnathias, from
COND (0) 9 ot FAW enim hen ot take Nac MMe ee ble. Egil eA AEM Ne LotR 133
WIRTH—A new species of Glutops and other new records of Se
MEA DATIOLOGA: 0 Meek teh cel hi Ne, Fite Me kc parte A C8) fod 4 ee Se RT
SLATER & KNIGHT The taxonomic status of Oligotylus Van Duzee eal
Leptotylus Van Duzee, with the description of a new species of
Pesan ys set hey ce aa, Nn a hee a ad Foe tae aidan pea eS
SNELLING—Records of Exomalopsis sidae in California and Baja
Galifornta s2.4.c50e ls P eek betas Se MLS are ieee eee ets 145
MICHELBACHER & HURD—Monodontomerus montivagus Ashmead, a
parasite of Megachile centuncularis (Linnaeus)... 22.------eoeee--
LINQUIST—Flies attracted to decomposing liver in Lake County,
Ga E Oran Os he St Ed hk oe cee eee NS nl Te eg ge nee 147
GARNER—A case of reverse predation in the Carabidae.......-----------ee-ecen-ee- 152
HUSSEY—Two new species of Pselliopus and some distribution notes....153
LEECH—Leptidiella brevipennis (Mulsant) reared from toyon.............--
LEE—tThe absence of negative phototropism in the Mexican chicken bug,
Haematosiphon indorus (Duges).
SAN FRANCISCO, CALIFORNIA « 1954
Published by the PACIFIC COAST ENTOMOLOGICAL SOCIETY
in cooperation with THE CALIFORNIA ACADEMY OF SCIENCES
THE PAN-PACIFIC ENTOMOLOGIST
EDITORIAL BOARD
E. G. LINsLEY P. D. Hurp, Jr., Editor R. L. Usincer
E. S. Ross H. B. Leecu
R. C. MI.ier, Treasurer A. E. MIcHELBACHER, Advertising
Published quarterly in January, April, July, and October with Society Proceed-
ings appearing in the January number. Papers on the systematic and biological
phases of entomology are favored, including articles up to ten printed pages on
insect taxonomy, morphology, life history, and distribution.
Manuscripts for publication, proof, and all editorial matters should be addressed
to P. D. Hurd, Jr., at 112 Agricultural Hall, University of California, Berkeley 4,
Calif. All communications regarding non-receipt of numbers, changes of address,
requests for sample copies, and all financial communications should be addressed
to the treasurer, Dr. R. C. mae at the lg iat Academy of Sciences, San
Francisco 18, Calif.
Domestic and foreign subscriptions, $4.00 per year in advance. Price for single
copies, $1.00. Make checks payable to “Pan-Pacific Entomologist.”
Announcing...
REVISION OF THE SPIDER MITE oe
TETRANYCHIDAE
by A. Earl Pritchard and Edward W. Baker
This world-wide treatment (300 pp., 330 figures) of the “Red
Spiders” is the second volume in the Memoirs Series of the Pacific
Coast Entomological Society. Each species is beautifully illustrated
in the inimitable style of E. W. Baker. The work deals with the
systematics, identification, and economics of the “Red Spiders”.
Synoptic keys have been prepared, descriptions are presented for
all species including the major agricultural pests, and some twen-
ty species are described as new.
Publication date—December, 1954.
Special Prepublication Price: $9.00.
Send orders to: Treasurer, Pacific Coast Entomological Society,
California Academy of Sciences, Golden Gate Park 18, San Fran-
cisco. For your convenience, an order sheet is found in this issue,
facing page 160.
Entered as second class matter, February 10, 1925, at the post office at
San Francisco, under act of August 24, 1912.
The Pan-Pacific Entomologist
Vol. XXX April, 1954 No. 2
SWARMING OF ANTS ON WESTERN UNITED STATES
MOUNTAIN SUMMITS
Joun A. CHAPMAN
Forest Biology, Science Service, Dept. of Agriculture, Victoria, B.C.*
In July, 1951, surprising numbers of insects were noted at the
top of an 8,000 foot mountain near Missoula, Montana. During
the following year, many personal conversations about summit
insects were held with men who had manned U.S. Forest Service fire
lookout stations at various times in the past. These conversations
revealed that gatherings of large numbers of winged ants on moun-
tain and ridge tops were of fairly common occurrence in western
Montana and northern Idaho and actually constituted a regular
and considerable nuisance at some lookout points.
A search through the literature on ants for information on
mountain top swarming yielded only a few observations from North
America, of unusually high altitude distribution of winged individ-
uals belonging to certain species, although some European records
of ant swarming and mating activity on hill and mountain tops
were found. It was felt that such an apparently widespread
phenomenon should be further investigated. A program was in-
itiated to try and secure additional information and observations
on summit swarming of flying ants from Forest Service personnel
located on the network of mountain top lookout stations through-
out the western United States, and also to study the phenomenon
locally, in conjunction with a general investigation of insect activity
on one nearby mountain summit.
A single data sheet which could be readily filled out was
prepared and the request made, through Forest Supervisors of the
various National Forests in the western United States, that copies
be placed with as many fire lookout observers as possible. This
form was accompanied by an explanatory note describing some
aspects of swarming behavior in ants and explaining the study
program. The information supplied through these forms for the
summer of 1952 as well as some data from previous years, based
upon the memory or records of various individuals, was sum-
* This study was accomplished while the writer was on the staff of Montana
State University.
94, THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
marized and analyzed. About 30 persons who had observed summit
ant swarms themselves were personally interviewed.
Summit swarming of ants was studied locally on Squaw Peak,
altitude 7,996 feet, about 25 miles northwest of Missoula, Montana.
This peak is rather isolated and has a fairly well defined summit
below which there are extensive slide rock areas with patches of
soil here and there supporting trees and alpine vegetation char-
acteristic of the region. Nine visits were made to this peak during
the period from late June to early September, 1952. Winged ants
were directly taken and observed on July 28, 29, August 3, 8, 9 and
September 2 and were collected at various times from pans of oil-
covered water which were set out on and near the summit on June
28 and left until August 26 or September 2. These pans were of
two sizes, 12x19x2 inches and 16x25x314 inches and one of each
size was placed at each of three stations whose relationship to each
other is as follows: station A, summit, altitude 7,996 feet; station
B, 163 feet from A, altitude 7,972 feet; station C, 173 feet from
B, altitude 7,921 feet. The two lower stations were located at 290°
with respect to the highest station. Small patches of soil and vegeta-
tion occurred at station A, but substrate at stations B and C con-
sisted entirely of large lichen-covered rocks. Insects from the two
pans at station C were kept together as were those from station B
pans. The small pan (station A,) at the summit was located on a
four and one half foot cairn while the large pan (station A.) rested
on the adjacent summit surface. After these two pans were found
to differ greatly in the number of ants trapped all insects from
them were kept separately. On days when direct observations were
made the estimated abundance, distribution on and around the
summit, mating activity, and general behavior of winged ants were
frequently noted. Altogether about 39 hours were spent in actual
study and observation of general insect activity on and near the
summit at times when winged ants were present.
Condensed and sumarized data from summit lookout stations
are presented in Figure 1* and in Table 1’.
It should be recorded that many of the lookout station observers
supplemented the information on their data sheets with more or
1 Base map supplied through courtesy of McKnight and McKnight Publishing
Co., Bloomington, Illinois.
2Tt is regretted that the help of the large number of fire lookout observers and
District Rangers of the U. S. Forest Service who supplied information used in this
study cannot be individually acknowledged here. .
APRIL, 1954] CHAPMAN—ANTS 95
less detailed accounts of the ant swarming seen. These accounts
agree with the descriptions of most persons who were personally
interviewed and with the observations of the writer on Squaw Peak
in consistently indicating 1) the location of swarms to be tops of
mountains or ridges and 2) a definite restriction of the swarms to
a rather small area at the actual summits, usually the highest
object or objects there such as roof, windows and external stove
pipe of the cabin, and in a few cases the tops of trees immediately
NONE
100S
1000S_ -
10,000S e
Fig. 1 Map showing distribution of reports of summit ant swarming.
96 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
adjacent to the summit as well. Frequently, when cabins were
elevated on towers (which ranged up to 90 feet in height) swarms
would be present by or on the cabins but not on the surface of
the ground below.
TABLE I. CONDENSED AND SUMMARIZED INFORMATION
FROM LOOKOUT STATION OBSERVERS
Number of Number of
Reports Reports
Total ....... . . 256 Altitude—all swarms of ants
Size swarms (maximum num- ON 2:000sftiy e's ee eA HO
bers reported from any area) 2000-4000) 83. a ae a
TQS ION, Segin <e ieee ie te wie 4:000.= 6,000 ft 5 2 Fee aS
NGOs.) ao ree ee 6,000- 8,000ft. . . . . . 89
AOOOOS: 46 ee s Jt Maye. Oo 35000 10/000 Tt. >. 2s ~ nv 48
Mating of ants absoreeak. eee GS over 10,000 ft. ass,
Shedding of wings observed. . 36 Altitude—swarms af tens oA
Maximum numbers ants on thousands of ants
relatively warm calm days 2O00> “AL000 TES oy BO 6
(wind less than 3 m.p.h.) . 118 4.000:- -6:000utt Stee, 4 = 28
Location of swarms at actual 6:000% 8.000 ST he ae ers
summit or top of ridges and 3,000 LOO00ttS se AS
mountains . . . dias 240 over 10,000 ft. Pate gor i At eae
Time of day at which swarms Time of year at ick
were reported to occur swarming was noted
e- sbOeARVIEN ED 9 2. Oe ts en 1382 Mary? als a ee Mal 2
LOR AAs rs Sees Ae ene 64 une say ae ee ee OK
Le em | edt eh oe be LOD uly ees Be! Asie tute ea Oh, © LOG
2 abe tae ase RS Ae USES wah Sie Bae Dy bale Oetes
4- 6P.M. 4] September... . 40
Some does “a lous ‘lsent ation is necessary in pide to stot
serve mating activity in swarms, and it was consistently noted on
Squaw Peak at times of even light swarming. It is therefore felt
that this activity is probably quite a consistent feature of summit
swarming.
Shedding of wings was reported relatively few times, This might
be due to the inconspicuous nature of the process or to the tendency
of dealate females to seek shelter and thus be overlooked. However,
no wing shedding was noted on Squaw Peak. Also, many observers
described such large invasions of lookout cabins by the winged ants
that they died in great numbers there, while at the same time
stating that no shedding of wings was seen. Seevral persons inter-
viewed stated that they had not noticed loss of wings and felt
fairly certain that, because of the large numbers of winged ants
present, they would have observed this had it been widespread.
ApRIL, 1954] CHAPMAN—ANTS 97
Several collections of winged ants which occurred in summit
swarms were sent in with the data forms. The ants represented and
the number of samples in which each was found are as follows:*
Formica sanguinea subnuda Em... . . . . . . 24
Formica sp. (microgyna group)
Formica sp.( fusca group) .
Formica sp. (sanguinea group) .
Formica sp. ; re Aa
Leptothorax eae ae
Leptothorax sp. .
Myrmica aldrichi (Whir.)
Myrmica lobicornis fracticornis Em. .
Myrmica (Myrmica) sp.
ho) SOO e ee
—
om)
On the days when the writer scp he flying ant activity
on Squaw Peak there was no doubt about the preference of the ants
for the actual summit and, in the case of Formica sanguinea sub-
nuda, for the two cairns on the summit (one eight feet and the
other four and a half feet high). These ants were observed on July
29, August 3 and 9 to congregate in numbers (up to several hun-
dred) on the upper rocks of the cairns, where they would crawl
about actively and where mating took place. There always appeared
to be many more males than females, a difference which showed
up in most samples of this species which were set in by lookout
observers. Counts made of samples of pan collected specimens
gave the following ratios of males to females: 377 to 33, August
3; 377 to 16, August 9; 377 to 15, August 26.
Leptothorax canadensis, noted in hundreds on July 29, ap-
peared to form loose flying groups to the leeward of the smaller
cairn and only scattered individuals were seen elsewhere at that
time. Data from the oil-water pans, given in Table II, show
clearly that for both of these ants preference for the summit itself,
and in the case of F. sanguinea subnuba the cairns specifically,
exists. Differences in relative numbers of L. canadensis taken by
large and small summit pans suggest some shifting of specific
swarming site of this species about the summit. No aggregations
of either species were seen away from the actual top of the peak
although surrounding lower areas were frequently visited in order
to determine swarm distribution.
Maximum numbers of ants were noted on relatively warm
calm days. At these times the ants could be seen flying about at
3 All specimens were identified by M. R. Smith, U S Nationa) Museum.
98 THE PAN-PACIFIC ENTOMOLOGIST [ VoL. XXX, NO. 2
the summit without being apparently influenced by air currents. At
other times the ants seemed to have difficulty reaching and main-
taining themselves on the cairns against the force of the wind.
There is no doubt about the presence of eddies of air currents
around the summit. At times, for example, southwesterly winds of
eight to eleven miles per hour were measured there, while 20 to 50
feet down on the east side (10 to 50 feet in vertical elevation)
velocities were close to zero. However, ants were never seen to
swarm at such points.
TABLE II. ANTS COLLECTED BY OIL-WATER PANS ON AND
NEAR SUMMIT SQUAW PEAK
Date of Station A; Station A: Station B Station C
Collection* Cairn Summit
Surface
July 3 larges 109 (ants from 0 0
small, 5 Station 0 0
A; andA,
combined )
July 15, large 522 not noted of 0°
small not noted _not noted not noted not noted
July 29 large 1418 400 5 5
small 2285 3477 34 3
August 3 large 7922 265 26 8
small 10244 3468 963 211
August 9 large 2701 238 9 6
small 2511 3340 342 125
August 26; large 2090 268 14 4
small 695 5310 552 187
September 2 large 8 not used not used not used
small 13
There are limitations to the use and intepretation of the in-
formation secured from fire lookout observers. Much of it was
furnished by persons lacking technical training in biology and may
be incomplete and even incorrect. Frequently only part of the
information requested was given. Many of the lookout stations
from which reports were received were manned only during certain
periods of the summer, depending on area fire danger ratings, and
* Pans set out June 28.
5 Mostly Formica sanguinea subnuda Em.
5° Mostly Leptothorax canadensis Prov.
7 Pans all dry on these dates.
8 Small pans only were checked.
APRIL, 1954] CHAPMAN—ANTS 99
thus do not include all instances of swarming which might have
occurred. However, many observations had undoubtedly been
carefully made and the data as a whole probably provide a reason-
ably good picture of many aspects of mountain summit ant swarm-
ing in the areas represented.
In trying to determine the causes of summit abundance of
winged ants it is necessary to carefully consider the possible effects
of wind on these ants. Complex air currents are a characteristic
feature of mountainous regions. The topography influences and
modifies large air mass movements in one direction and heating
and cooling of the varied land surfaces, due to gain and loss by
radiation during the day and night, respectively, produce varied
local air movements. Fire control studies in the northern Rocky
Mountain region by the U. S. Forest Service (Barrows, 1951) have
shown that, as a general rule, upslope winds commence around
9:00 A.M. and continue until late afternoon when, after a short
transition period, downslope winds occur. It is logical to assume
that updraft air currents play a role in mountain top ant swarming.
It is known that air currents can transport ants as well as other
insects to considerable distances above the surface of the earth
even under relatively mild weather conditions (Glick, 1939). In
many ant species the reproductive forms leave different nests within
an area at much the same time so that some temporary abundance
of winged ants may be noted in almost any locality. (Forel, 1875,
1930; Emery, 1891; Wheeler, 1910). If ants emerge at lower
elevations during the day any updraft currents would tend to carry
them upwards. Winged ants are not considered to be strong fliers
and almost any air movement in a particular direction might be
expected to affect their distribution. Once ant reproductives were
present in numbers on a summit, one would expect their mating
activity to proceed as it would below.
It is interesting to note that in 118 of the reports from lookout
stations and also at Squaw Peak, maximum numbers of ants were
observed on warm calm days, if winds of three miles per hour and
less are included in the calm category. Many ant species tend to
swarm on such days at lower elevations. It is recognized that
thermal updrafts are probably more clearly defined and therefore
relatively more important as transporting agents on these warm
calm days than at other times where more general air movements
may play the dominant role.
100 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
Continuous measurements of air currents around a peak coinci-
dent with summit abundance of winged ants have not been made.
The actual extent to which updrafts of various velocities might
tend to carry ants of different sizes and flight powers likewise is
not known although there is evidence, in abnormally high distibu-
tion of scattered ant reproductives, that air currents can transport
ants upwards for considerable distances. Wheeler (1917a, 1917b)
suggested that in mountainous regions winged ants were frequently
carried above the normal species range by air currents and that
annual loss of such individuals in terms of potential colony estab-
lishment might cause a considerable drain on certain species.
It is not yet possible to completely evaluate the role of updraft
air currents as they may relate to summit ant swarming. However,
there are several indications, based both on the writer’s study on
Squaw Peak, and on the data secured by others, that the ant swarms
observed cannot be accounted for by air currents alone.
Probably the main difficulty in explaining summit swarming
entirely on the basis of air currents is the apparent localization of
ant swarms, of all sizes, at the actual tops of mountains and ridges
and frequently within small areas on the summits. The Squaw
Peak pan collection data show a very clear preference for the actual
summit. Moreover, concentrations within a small area were repeat-
edly described by the lookout observers. There were far more op-
portunities for these observers to notice the ant swarms at summits
that at lower elevations due to the fact that almost all lookout
stations are located on the highest points of mountains or ridges.
However, it was specifically reported by several persons that
areas below the summits were visited during periods of swarming,
and it can be assumed that there were many more observations
made away from the highest points during such times in view of
the following points: 1) swarming was frequently reported to be
of several days duration, 2) leave and activities such as trail main-
tenance and transportation of water, for example, require that
observers be away from the summit at times. Actually not a single
person reported simultaneous swarming of ants at lower elevations
and at summits.
Lookout stations from which “tens of thousands” of ants were
reported ranged from 2,600 feet to 11,030 feet in altitude and in-
cluded bare rocky peaks, where thermal air currents might be
expected to be fairly strong, and grassy or brush and forest covered
APRIL, 1954] CHAPMAN—ANTS 101
ridges and hills, where thermals are certainly not as well developed.
It might be noted that in all but a few cases reported by fire lookout
observers only one or two kinds of ants were seen to swarm at any
one summit.
Forel (1875, 1930) reported that swarms of Myrmica rubra,
and of other species presumably, at times would form over standing
men, roofs of houses, tall trees, church steeples, hill summits and
even mountain tops and he recorded some summit mating activity
for several species of ants.
It is hard to believe that air currents alone would produce such
large localized concentrations of ants and at sites such as some of
the points mentioned by Forel, or reported by lookout observers,
or the cairns on Squaw Peak. One would expect wind or updraft
carried insects to be scattered along the approaches to distinct
peaks and throughout the length of ridges, since there is certainly
some eddying of air currents below or near the highest point in
either case. As a matter of fact one could also expect that updraft
currents strong enough to be a major factor in carrying insects
would tend to transport them on up above and away from the
ridgetops or peaks. It is interesting to note in this respect that
several other types of insects tend to be more abundant on mountain
peaks and summits than below such areas (Chapman, 1954).
In summing up the consideration of air currents as the cause
of summit abundance of winged ants it would seem that although
such currents may play a role, a definite preference for the summits
of ridges and mountains as swarming sites is shown by some ant
species.
It is hoped that future work may provide more specific informa-
tion on distribution of various summit swarming species, on the
fate of winged ants after swarming, including the extent of wing
shedding by females, on the duration of swarming for various
species, distances through which summit ants may travel and on
a number of other phases of this phenomenon which are not well
known at present.
SUMMARY
Information and observations on the swarming of winged ants
on mountain summits were secured from persons stationed at
summit fire lookout stations throughout mountainous regions of
the western United States during the 1952 summer season. Some
records from years prior to 1952 were also obtained. This data was
102 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
recorded for the most part on a form which proided for systematic
recording of desired information, and is summarized, analyzed
and discussed in this report. Studies of mountain top ant swarming
were also made by the writer on an 8,000 foot mountain near
Missoula, Montana. Insects were collected and observations made
at intervals during the summer of 1952 and the resulting data
presented and discussed. It is felt that the following conclusions
are justified:
1. Swarming of winged ants of certain species at the very
summits of peaks and ridges is a definite and fairly widespread
phonomenon in many of the mountainous regions of the western
United States.
2. Although it is not possible at present to accurately determine
the role of updraft air currents in producing such swarms it is
unlikely that updrafts are the only casual factor.
3. An instinctive tendency to seek such points as swarming
sites is probably present in some ant species.
LITERATURE CITED
Barrows, J. S.
1951. Fire behavior in northern Rocky Mountain forests. Northern
Rocky Mountain Forest and Range Experiment Station, Missoula,
Montana. Station Paper No. 29.
CHAPMAN, JOHN A.
1954. Studies on summit-frequenting insects in western Montana. Ecol-
ogy, 35 (1): 41-49.
Emery, CarLo
1891. Zur Biologie der Ameisen. Biol. Centralblatt 11:165-180.
Foret, A.
1875. Les fourmis de la Suisse. Nouv. Mem. Soc. Helv. Sci. Nat.
Vol. 26.
Fore, A.
1930. The social world of the ants compared with that of man. 2 Vol.
Trans. C. K. Ogden A. and C. Boni New York.
Guick, P. A.
1939. The distribution of insects, spiders, and mites in the air. U. S.
D. A. Tech. Bull. No. 673.
Wuee er, W. M.
1910. Ants, their structure development and behavior. Columbia Uni-
versity Press, New York.
Wuee ter, W. M.
1917a. Notes on the marriage flights of some Sonoran ants. Phyche
24:177-180.
Wuee er, W. M.
1917b. The mountain ants of western North America. Proc. Amer.
Acad. Arts Sci. 52(8) :457-569.
APRIL, 1954] EVANS—TASTIOTENIA 103
THE MALE OF TASTIOTENIA FESTIVA
(Hymenoptera, Pompilidae)
Howarp E. Evans
Cornell University, Ithaca, N.Y.
A few years ago I described an unusual new genus of pompilid
wasps, Tastiotenia, based on two females, one from Needles, Calli-
fornia, and one from Guaymas, Sonora, Mexico (1950, Trans.
Amer. Ent. Soc., 75:150). In the description a number of curious
morphological features were pointed out, and the unique wing
venation was described and figured. It was concluded that the
genus apparently belonged to the tribe Pompilini, but that it must
represent a relict of a very early type. I have awaited the discovery
of the male of this genus with considerable anticipation. Fortu-
nately I have not had to wait long, for an intrepid wasp-hunter,
Dr. Paul D. Hurd, Jr., has recently collected a male Tastiotenia at
Borego, San Diego County, Calif., May 2, 1952. Although differing
in color from the female T. festiva, the difference is no greater
than often occurs between the sexes in Pompilidae, and I feel cer-
tain that it represents the male of this species. The male keys readily
to Tastiotenia in my key to the Nearctic genera of Pompilini, and
the wings are virtually identical with those figured.
The male possesses all the unusual features of the female plus a
tew of its own, notably the flattened and somewhat expanded hind
basitarsus and tibial spurs, and the oddly shaped last antennal
segment. The terminalia, however, are remarkably conventional,
and on the basis of these alone one might easily place festiva in
the genus Pompilus, in fact close to phoenix. It is difficult to believe
that these resemblances are more than coincidental. However, the
placing of Tastiotenia in the Pompilini seems thoroughly justified
on the basis of the genitalic structures.
Description of male——Length 4.5 mm.; fore wing 3.8 mm. Posterior mar-
gin of pronotum with a prominent ivory-white stripe, including the posterior
lobes, and the apical abdominal tergite with a large white spot; posterior
femora bright rufo-ferruginous, dusky at base and apex; apical half of man-
dibles rufous; color otherwise black. Wings hyaline, the apical fourth of the
fore wings lightly banded with brownish. Body clothed with a somewhat
coarse silvery pubescence, more dense and suberect on the propodeum;
pubescence grading into brownish on the extremities of the legs. Mandibles
with a single strong tooth on the inner margin. Clypeus 3.5 times as broad
as high, the apical margin broadly, weakly concave. Malar space extremely
short. Front very broad, the middle interocular distance .66 times the trans-
facial distance: inner orbits approximately parallel, the upper and lower
104, THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
interocular distances about equal. Ocelli rather widely separated on the ~
broad vertex, forming a right angle in front; postocellar and ocello-ocular
distances about equal. Vertex elevated in a low, even arc above the eye-tops.
Antennae short; first four segments in a ratio of about 17:9:8:10, the third
segment thus actually shorter than the pedicel, and only very slightly longer
than thick; outer flagellar segments (7-12) approximately as long as their
greatest thickness; apical segment about 1.5 times as long as thick, its apex
abruptly, obliquely flattened. Pronotum short, its posterior margin feebly
angulate. Scutellum very prominent; postnotum approximately as wide as
the metanotum, distinctly impressed medially. Propodeum without a well-
defined posterior rim. Legs feebly spinose; femora with one or two minute
spines near the apex; middle and hind tibiae and tarsi with scattered very
small spines. Hind coxae large, about 1.5 times as long as the middle coxae.
Hind tarsus compressed, the basal segments somewhat expanded; basitarsus
considerably broader than the tibia at its base; longer spur of hind tibia
broadened and flattened, narrowly fusiform (shorter spur of hind tibia want-
ing in this specimen). Tarsal claws feebly dentate. Wings as described and
figured for the female in the original description. Abdomen short and rela-
tively stout, the dorsum somewhat flattened, the sides rather flat and con-
verging below, the abdomen in cross-section therefore somewhat trigonal.
Sixth sternite deeply emarginate apically, without special modifications.
Subgenital plate (fig. 2) with the median line roundly elevated, the apex
narrowly rounded and the margin beset with stout spines, except the extreme
apex with only weak setae. Genitalia (fig. 1) with the parameres very slender,
clothed with short setae on the apical two-thirds; volsellae with the digiti
broadly expanded apically and clothed with short setae; basal hooklets
double; aedoeagus with a broad fan-shaped apical expansion.
EXPLANATION OF FIGURES
Figure 1—Male genitalia of Tastiotenia festiva Evans, ventral aspect on
left side, dorsal on right. Figure 2—Subgenital plate, ventral aspect.
APRIL, 1954] CHANDLER—DOBSONFLIES 105
FOUR NEW SPECIES OF DOBSONFLIES FROM CALIFORNIA
(Megaloptera: Corydalidae)
Harry P. CHANDLER
California Department of Fish and Game, Red Bluff, California
Two of the species were suspected of being new when they were
first collected in 1946 along with another new species which is
being described elsewhere by a student who has worked out its
life history. The other two species described here were discovered
while working over the California Insect Survey and California
Academy of Sciences collections during the preparation of the
section on California Megaloptera for a book on the aquatic insects
of California to be published by the University of California.
There are still several undescribed species or subspecies in the
west, but the author prefers not to describe them at this time be-
cause the picture of their speciation and distribution is not clear
at present. Since the Nearctic species of this group were last
keyed by Davis in 1903, the number of described species has
doubled; and from the species included in Chauliodes have been
separated four other genera. Van der Weele’s world revision in
1910 threw considerable light on the generic picture but com-
pletely confused the species by placing in synonymy about half
of the valid Nearctic species. In view of this, the author plans
to revise the Nearctic Corydalidae in the near future.
Dysmicohermes ingens Chandler, new species
Holotype male: Alar expanse 122 mm.; body predominantly testaceous
brown, sparsely covered with conspicuous long, silky hair. Head rufous,
coarsely and closely punciate, except for smooth raised area on vertex:
labrum transverse elyptical; clypeus smooth but otherwise poorly differen-
tiated from front, apex straight, angled at sides and nearly straight to margin
of eye. Antennae with 52 segments, filiform, relatively short, length about
three times width of head, each segment a little longer than wide, covered
with short microscopic pile, and sprinkled with short, depressed spines about
Y4 as long as segment. Ocelli parallel with outer margin of antennae, middle
ocellus less convex, 4/5 as wide as lateral ocelli, ocelli separated from an-
tennae by about own width, middle ocellus separated from lateral ocelli by
width of latter, lateral ocelli more widely separated from each other; cheeks
of head parallel a little distance behind prominent eyes; mandibles mostly
concealed when closed. Pronotum with sides nearly parallel, slightly con-
vergent anteriorly, faintly alutaceous with fine punctures, covered with a
short sparse pubescence. Wings (fig. 5), slightly translucent, stimga more so;
veins brownish, not conspicuously variegated; fore wing with translucent
brown spots, with slight tendency to be arranged along the veins, spots quite
small except near the basal 1/5 and 2/5 of the wing where they form two
106 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
indistinct transverse bands. Hind wings more faintly spotted basally and
posteriorly, none behind the cubitus. Radial sector with seven branches
reaching margin, media two-branched in fore wing and four-branched in hind
wing; cubitus three-branched. Fore wing with base of Ist anal conspicuously
raised and covered by most pronounced black spot on wing; anterior branch
of 2nd anal vein connected to the first anal by a cross vein which forms end
of Ist anal cell, posterior branch of 2nd anal vein forming end of 2nd anal
cell. Genitalia (figs. 3, 4), cerci with a deep cleft between the upper and
lower lobes, reaching more than half way to base or nearly to convex pitted
area on the lateral dorsal side near the base, anterior margin on ventral
lateral side with deep emargination partially filled by base of an elongate
osmeterium-like eversible membranous iube which may be withdrawn into
the body, length of tube is about 2.5 times the width of the genital capsule,
tube tapering to a point.
Allotype female: Alar expanse 160 mm.; very similar to male but larger.
Genitalia; valves of ovipositor with convex pitted area near base, upper lobe
short, lower lobe 214 times as long, narrowed to middle.
Holotype, Miamt Rancer Station, Mariposa County, CALt-
FORNIA, 27 July 1946, elev. 5,000 feet (H. P. Chandler). Allotype,
same data as holotype. Six paratypes are from the same locality
and collected by H. P. Chandler in 1946 except as noted; 6’, 29
June, &, 6 July; 20 3, 21 July; &, 23 July; 2, 29 July 1946 (T.
O. Thatcher). One 2 paratype from Sequoia Nat. Park, California
and one 9 from San Bernardino County, 1916, “Viggo Tarp.”
Holotype and allotype in the California Academy of Sciences col-
lection. Paratypes in the California Insect Survey collection, Los
Angeles County Museum, Museum of Comparative Zoology and
the author’s collection.
This species is closely related to D. disjuncius (Walker). The
shape and venation of the wings are almost identical, but the
coloration is different. In D. disjuncius the spots are larger, more
intense and the membrane more hyaline, the head is less strongly
punctured and more rugose, the ocelli a little smaller and the
' tranverse depression behind the eyes less pronounced, the four,
medial, basal, raised areas on the vertex are separated by a
medial and transverse groove of even width so as to form a nearly
perfect cross. The genitalia as figured by Munroe (1953), while
very similar in type is different in almost every detail.
With the possible exception of Acanthacorydalis which is
found in the Orient, D. ingens has a larger wing spread than any
other species in the order Megaloptera.
All except two specimens of D. ingens listed above were taken
Aprit, 1954] CHANDLER—DOBSONFLIES 107
in the summer of 194.6 when the University of California entomol-
ogy field class used the U. S. Forest Service insect laboratory at
Miami Ranger Station just five miles south of Yosemite National
Park. Most of the specimens were taken around a light trap that
was operated part of the time. They were rarely taken in the trap
or seen fluttering about it but were found at rest on some object
near by. Apparently they came from a small stream that passed the
camp on its way down the side of the canyon. Dr. Struble, one
of the laboratory staff, on his way to work one morning, found a
cast pupal skin about 20 feet from the stream. Knowing my interest
in the adults, he located, about 6 inches away in the bank, the
hole from which it had emerged. No larvae were ever taken.
Dysmicohermes crepusculus Chandler, new species
Holotype male; alar expanse 84 mm.; body color dark brown to pale,
long hair very sparse and inconspicuous. Head dark brown to rufous with
mouthparts and adjacent areas pale, except for black tip of mandibles;
dorsal surface of head from clypeus to behind ocelli wrinkled and with
microsculpture of short parallel ridges, from the eyes posteriorly micro-
sculpture is more rugose with close set short, depressed hairs; smooth areas
of vertex faintly alutaceous, scarsely raised or even slightly depressed. Lab-
rum narrowly transverse, anterior margin straight with small emargination
at middle, front marginated anteriorly with pale color, clypeus very narrow,
depressed and smooth. Antennae about 3 times as long as width of head,
fuscous brown, 35 segments, filiform tapering to end except basal segment
which is nearly twice as wide as next few segments, segments about 3 times
as long as wide, spinkled with short distally inclined spines 1/3 width of
segment, micropile scarsely detectable on the basal segments. Outer margin
of ocelli parallel with inner margin of antennae, ocelli separated from each
other by width of lateral ocelli which are a little smaller, separated from
antennae by 1.3 times width of median ocellus, diagonal ridge separating
depressed area around ocelli from eyes. Mandibles mostly concealed when
closed. Pronotum with sides slightly concave, a little wider anteriorly, color
brown with anterior pale collar tapering to point at each side, microsculpture
alutaceous, tending to short parallel ridges posteriorly and laterally; devoid
of long pubescence, only a few short hairs near anterior and posterior mar-
gin. Wings (fig. 6), translucent; veins pale, not conspicuously variegated,
both wings except anal area of hind wing spotted with moderate to small
fuscous spots with slight tendency to form one or two transverse bands.
Base of first anal of anterior wing moderately raised without entire raised
area black. Costal area of fore wing widest at basal 14 where it is wider than
other cells of wing. Radial sector with seven branches reaching margin, Rs
forked beyond its middle; media two-branched in fore wing and _three-
branched in hind wing, cubitus with three branches reaching margin. An-
terior branch of second anal vein connected to first anal vein by cross vein
108 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
only, which forms end of first anal cell, posterior branch of second anal vein
forming end of second anal cell. Genitalia (figs. 1, 2) : cerci very short, upper
and lower lobes represented by slight protuberances separated by a horizontal
groove around end of cerci, ending near base of convex punctate area,
eversible parallel-sided membranous tube three times as long as width of
genital capsule, located on each side anterior to and below cerci.
Allotype female: alar expanse 106 mm.; generally similar to male except
that sculpture and proportions of head are slightly different; white collar
of pronotum less distinct; genital valves with upper and lower lobes barely
projecting beyond convex pitted area which occupies most of side.
Holotype, PyRAMiIp RANGER STATION, ELpDoRADO County,
Catirornia, 20 Aug. 1952 (J. W. MacSwain); allotype, 2 mi.
S.W. Miami Ranger Station (Girl Scout Camp, N. Fk. Fresno
River), Mariposa County, California, 25 July 1946, elev. 5,000
feet (H. P. Chandler). Twenty-seven paratypes from California
and one from Oregon as follows: Mono Co.: 9, Convict Cr. Ex-
perimental Sta., 12 Aug. 1953, elev. 7,200 (I. La Rivers); Mari-
posa Co.: 9, 2 mi. SW. Miami R. S., July 1946 & & 2, Girl Scout
Camp, N. Fk. Fresno River, July 1953, elev. 5,000 (Girl Scouts) ;
©, Nevada Falls, 29 July 1946, elev. 5,950 feet (H. P. Chandler) ;
2, Yosemite, Aug. 1935 (E. S. Ross) ; Nevada Co.: 3, Grass Valley,
July 1942 (L. Bwd.); Sierra Co.: &, Goodyear Creek, 10 July
192] (E. H. Nast); Plumas Co.: 3, 4 mi. W. Quincy, 26 June
1949 (J. W. MacSwain) ; Butte Co.:¢, Chico, 23 July 1951 (Ber-
riman); Shasta Co.: &, Burney Creek Hatchery, 15 July 1947
(D. W. Adams) ; Siskiyou Co.:¢', Dunsmuir, 30 June 1934 (G. H.
& J. L. Sperry); 3 é co S. Fk. Sacramento River, 6 Aug. 1953
(H. P. Chandler) ; Colusa Co.: 11 ob ob, 3 99, Paradise Creek, 23
July 1953, elev. 2,400 (H. P. Chandler) ; Lake Co.: &, Anderson
Springs, 12 July 1953 (W. R. Bauer); and one ¢ collected by
Behrens, who died in 1898, labeled “Francisco.” Oregon, Marion
Co.: &, Breitenbush Hot Springs, 5 July 1934, elev. 2,222 feet
(H. A. Scullen). The holotype and allotype will be placed in the
California Academy of Science collection; paratypes in the Cali-
EXPLANATION OF FIGURES
Fig. 1. Dysmicohermes crepusculus, lateral view of male genitalia. Fig.
2. Ventral view of the same. Fig. 3. D. ingens, lateral view of male genitalia. .
Fig. 4. Ventral view of the same. Fig. 5. Wings of D. ingens. Fig. 6. Wings
of D. crepusculus. Fig. 7. Protochauliodes simplus, ventral view of tip of
aedeagus. Fig. 8. P. simplus, lateral view of cerci. Fig. 9. P. montivagus,
lateral view of cerci. Fig. 10. P. montivagus, ventral view of tip of aedeagus.
Apri, 1954] CHANDLER—DOBSONFLIES 109
SSSA YT
SSS SST
LES OPE EEE aw,
Wp
110 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 2
fornia Insect Survey collection, Illinois Natural History Survey
collection, Chico State Teachers College collection, Museum of
Comparative Zoology and the author’s collection.
This species is provisionally placed in Dysmichohermes but is
not closely related to either D. disjunctus or D. ingens. From these
two species it is most easily separated by its smaller size, the wide
costal area of the fore wing, the hind wing with three branches
of the media reaching the margin, and the genitalia. There is
some variation in the specimens studied but it is difficult to de-
scribe. The number of segments in the antennae range from 35 to
47, seeming to be a little more numerous but shorter in the female.
The antennae of the males were usually about 2.9 times as long
as the width of the head, while those of the female were only about
2.2 times. The alar expanse in the males ranged from 67 mm. to
98 mm. while that of the females ranged from 100 to 108 mm.
Other variations were noted, especially in the proportions and
sculpturing of the head. The latter seemed a little more pronounced
in the female.
Protochauliodes simplus Chandler, new species
Holotype male: Alar expanse 78 mm.; general body color fuscous with
lighter markings, body with little hair except ventrally. Head fuscous brown,
pale in front of antennae. Labrum with sides rounded, slightly emarginate
medially. Antennae brown, 414 times longer than width of basal segments.
Ocelli large, median slightly smaller but as wide as front between antennae,
only about 1/3 its width from antennae, lateral ocelli separated from eyes
and median ocelli by own width, vertex behind ocelli not depressed but
evenly rounded from side to side, smooth areas alutaceous, not conspicuously
raised or darker, rest of vertex very finely rugose. Wings slightly translucent
with many small, smoky spots with a tendency to be arranged along sides
of veins and a few larger opaque spots along the anterior margin; fore wing
with a larger spot covering the first medio cubital cross vein; hind wings with
spots restricted to apical portion. Ras; unbranched, R. and R; forked at
apical third, Rs without cross vein between its two branches; anterior branch
of second anal vein stalking with first anal for a short distance, so that
latter appears three branched. Genitalia: cerci (fig. 8), somewhat dorso-
ventrally flattened basally; aedeagus (fig. 7), nearly flat.
Holotype, TANBARK Fiat, San Dimas ExpeRIMENTAL Forest,
Los AncELEs County, Catrrornia, 13 July 1950 (J. D. Paschke).
Ten paratypes, all males, were collected from the same locality by
A. T. MaClay (6), S. Miyagawa (2), E. G. Linsley (1) and D. E.
Barcus (1) on July 7 (1), 12 (1), 17 (1), 18 (1), 22 (2), 23
(4), 1952. The holotypes will be placed in the California Academy
APRIL, 1954] CHANDLER—DOBSONFLIES 11]
of Sciences collection with paratypes in the California Insect Sur-
vey collection, University of California collection at Davis, Los
Angeles County Museum and the author’s collection.
This species is related to P. infuscatus and P. minimus. The
wing veination and body form of the species in this group are re-
markably constant and sometimes the difference between species
is less than individual variation within the species. Except that
infuscatus is black and minimus is usually smaller, the only sure
way of separating the species is by examining the genitalia.
Protochauliodes montivagus Chandler, new species
Holotype male: alar expanse 72 mm.; description similar to that of
P. simplus except as noted. Lateral ocelli more than own width from eyes;
smooth areas raised a little, rest of vertex with microsculpture of short
parallel ridges. Wings with opaque spots more restricted, outer half of hind
wing faintly potted. Genitalia: cerci (fig. 8), short and stubby, as wide at
apex as at base as viewed from side; aedeagus (fig. 10), flat, only the tip
chitinized ventrally. ;
Holotype from St. CHARLES HILL, SIERRA CouNTY, CALIFORNIA,
7 July 1921 (E. H. Nast collector). Three paratypes, all males,
from Sierra City, Sierra Co., Calif., 25 July 1952 (Don Richtor) ;
Quincy, 4 mi. W., Plumas Co., Calif., 2 July 1949 (R. L. Lang-
ston); and Lake Vernon, Yosemite, Calif., 25 July 1937 (E.
Herald). The holotype will be placed in the California Academy
of Sciences collection. Paratypes will be placed in the University
of California collection at Davis, Los Angeles County Museum and
the author’s collection.
LITERATURE CITED
Davis, K. C.
1903. Sialidae of North and South America. New York State Museum
Bull. 68: 442-486, pls. 51, 52.
Munrog, E. G.
1951. The identity and generic position of Chauliodes disjunctus Walker
(Megaloptera: Corydalidae), Canadian Ent., 83(2): 33-35, 3
text figs.
Munrog, E. G.
1953. Chauliodes disjunctus Walker: a correction, with the description
of a new species and a new genus (Megaloptera: Corydalidae).
Canadian Ent., 85(5): 190-192, 4 text figs.
Wee.e, H. W. van DER
1910. Megaloptera, Catalogue systématique et descriptif. Coll. Zool.
Selys Longchamps, Brussels. Fasc. 5: 1-93, 70 text figs., 4 pls.
112 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
MODIFIED FLAG FOR TICK COLLECTING
During two seasons of tick collecting the author noted three
small cumulative disadvantages in the standard flagging method,
when collecting ticks among low grasses and weeds, with few trees
and bushes present. These were: (1) difficulty in obtaining maxi-
mum coverage of the flora because the flag was usually at an angle
to the ground; (2) difficulty in prevention of flapping by moderate
winds, and (3) inconvenience to the collector who was required
to bend sharply in order to hold the flags close to the low
vegetation.
To overcome these drawbacks, a flag was attached to a 3-ft.
equilateral triangle with the 6-in. handle at the apex, and the muslin
flag at the base. Each side was made of 3/16 in. steel wire, with
half of a threaded bolt tip welded to each of the two ends which
come together to form a handle attachment. To make the instrument
more compact, the handle was made removable and the sides con-
sequently folding, permitting one to wrap the handle and sides,
together with the base, in the muslin.
In use, the flag can be (1) held in front, which permits tick
collecting before the operator can jar or otherwise dislodge the
arthropods, (2) pulled behind as a drag cloth, and (3) pulled
beside the collector, on either side. Also, the flag is easily held
parallel to the surface to be collected, assuring thorough coverage;
kecause the instrument is easily controlled, slight movements by
the collector can prevent undue flapping, even in moderately high
winds, and there is a minimum of inconvenience to the collector.
Though adapted for low vegetation, this instrument will work
equally well on bushes and trees—W. PETER Horen, San Anselmo,
California.
RANGE EXTENSION OF NOTONECTA SHOOTERI
(Hemiptera: Notonectidae)
I collected two specimens of Notonecta shooteri Uhler at Port
Orford, Curry County, in a stream on July 7, 1951, and an ad-
ditional three specimens three days later at Charleston, Coos County,
in a pond. Both localities are located on Oregon coast. Marin County
in California represented former northernmost records of this
species. — Borys MALkin, University of Washington, Seattle.
APRIL, 1954] TODD—NERTHRA 113
NEW SPECIES OF NERTHRA FROM CALIFORNIA
(Hempitera: Gelastocoridae )
E. L. Topp
Entomology Research Branch, Agricultural Research Service
U.S. Department of Agriculture
During the course of a taxonomic revision of the family Gelasto-
coridae (Hemiptera), it was discovered that the genera Nerthra
Say and Mononyx Laporte are congeneric. As Nerthra was de-
scribed early in 1832 and Mononyx not until 1833,, the former has
priority and should be used as the generic name for those species
formerly placed in the genus Mononyx.
For many years Nerthra fuscipes (Guérin-Méneville) has been
reported from California, but these reports were misidentifications
of a new species that occurs in the southern part of this state. A
second new species has recently been collected in the vicinity of
Parker Dam, San Bernardino County, California, by Doctor R. L.
Usinger and Mr. Jack Lattin. The descriptions of these two species
are presented at this time so that the names will be available for
use in a faunal work.
Nerthra martini Todd, new species
Referring to this species:
1876. Mononyx badius Herrich-Schaffer; Uhler, Bull. U. S. Geol. Surv., pp.
336-337.
1894. Mononyx stygicus (Say); Uhler, Proc. California Acad. Sci., Ser. 2,
Vol. IV, pp. 290-291.
1917. Mononyx fuscipes Guerin-Meneville; Van Duzee, Catalogue of Hemip-
tera, Univ. of California Publ., p. 474.
Size. Male: Length, 7.0 to 7.6 mm.; width of pronotum, 4.5 to 4.8 mm.;
width of abdomen, 4.5 to 5.0 mm. Female: Length, 7.8 to 8.8 mm.; width of
pronotum, 4.8 to 5.3 mm.; width of abdomen, 5.0 to 5.8 mm. Color varying
from a yellowish-brown to black, generally a brown or reddish-brown. A
whitish spot on each hemelytron mesad of the junction of the embolial and
nodal sutures. In the black specimens the posterior third of the pronotum is
generally spotted with pale yellow or white. Ventrally slightly lighter than
dorsally; front femur uniform brown, intermediate legs light brown ringed
with dark brown areas which may be faint in some specimens; last three
abdominal segments lighter than rest of abdomen; connexivum with pos-
terior third of each segment yellowish, anterior two-thirds dark. A few
specimens examined were uniformly reddish-brown above and with a lighter
marginal band ventrally which extended the entire length of the abdomen.
Structural Characteristics. Apex of the head pointedly projecting with a
pair of rather sharp-pointed tubercles at the tip, sometimes these tubercles
1 Harris, H. M., Pan-Pacific Entomologist, Vol. 18, No. 1, pp. 161-162, 1942;
shows that Laporte’s paper did not appear in 1832 as s usually given.
114, THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
are rather rudimentary; superapical tubercles present. Pronotum not very
dilated laterally; lateral edge nearly straight, occasionally weakly sinuous
at middle; lateral edge conspicuously converging anteriorly; posterior mar-
gin sinuated before scutellum. Pronotum at greatest width not as wide as
abdomen in either sex. Scutellum broad, rather large, with slight tumescence
on either side, mesad of which of are faint rounded depressions. Body
sparsely covered with very small bristles, those on the scutellum being
slightly clavate. Hemelytra well-developed extending beyond the apex of the
abdomen. Lateral margin of the embolium nearly straight, not dilated. Con-
nexivum barely visible from a dorsal view in the male, quite prominent in
the female because the posterior abdominal segments are greatly dilated
laterally. Last abdominal segment of the male rather large, over half as wide
as the eighth abdominal segment, slightly longer than seventh or eighth
abdominal segments, asymmetrical. Ventral abdominal segments of female
asymmetrical; posterior margin of last abdominal segment more or less
pointedly notched; a moderate tumescence on the left side, a faint tumes-
cence on the right side of the last abdominal segment; a deep, elongate,
transverse depression extending along the anterior margin of the last abdom-
inal segment from the median line of the abdomen to the tumescence on the
left side. Clasper of male (fig. 1) swollen apically; a weak process on the
lateral surface and another on the dorsal surface: aedeagal furrow visible
- on the apical half of the ventral surface.
Holotype male, allotype female, 24 male and two female para-
types. Los Pensacuiros CREEK, SAN DiEco County, CALiFrornia,
April 8, 1930, C. H. Martin, in the Francis Huntington Snow
Entomological Collection at the University of Kansas. One male
and one female paratypes, San Felipe Creek, California, April 14,
1935, C. E. Norland, (Usinger Collection). One male and one
female paratypes, Los Angeles County, California, no date, Coquil-
lett, (U. S. Nat. Museum). One male and one female paratypes,
Riverside, California, March 2, 1927, T. Craig, (California Acad-
emy of Sciences).
In addition to the type series, the writer has seen specimens
from the following localities:
California. Afton Canyon, San Bernardino County, July 17, 1931, R. E.
Blackwelder, 1 male, (California Acad. Sci.) ; Ardeou, Dec. 25, 1915, J. C.
Martin, 1 female, (California Acad. Sci.); Frenchman Flats, Tehachapi,
April 8, 1951, R. L. Usinger, 1 female, (Usinger Collection) ; Los Angeles,
no date, P. R. Uhler, 1 male, (U. S. Nat. Museum); Palm Canyon, April
15, 1916, J. O. Martin, 1 male, (California Acad. Sci.) ; Palm Springs, Riv- -
erside County, April 3, 1925, E. C. Van Dyke, 1 male, (California Acad.
Sci.); same place, Jan. 3, 1929, Van Dyke, 1 female, (Univ. of Kansas
Coll.) ; same place, Aug. 2, Hubbard, 1 female, (U. S. Nat. Museum) ;
Panamint Valley, April 1891, C. V. Riley, 2 females, (U. S. Nat. Museum) ;
Pico, March 7, 1916, J. O. Martin, 1 male and 1 female, (California Acad.
ApRIL, 1954] TODD—-NERTHRA 115
Sci.) ; Pine Valley, July 27, 1938, R. I. Sailer, 1 female, (Univ. of Kansas
Coll.) ; Santa Ana Canyon, July 12, 1931, C. H. Martin, 7 males and 3
females, (Univ. of Kansas Coll) ; Sierra Madre, June 7, 1930, C. H. Hicks,
2 males, (Phila. Actd. Sci.) ; Sierra Nevada Mountains, no date, P. R.
Uhler, 1 male, (U. S. Nat. Museum).
Nevada. Warm Springs, Clark County, April 7, 1950, L. A. Rivers and
V. K. Johnson, 2 males (California Acad. Sci. and Usinger Coll.).
Arizona. “Ariz.”, no date, P. R. Uhler, 1 male, (U. S. Nat. Museum) ;
“Ariz.”’, no date, C. F. Baker, 1 male and 1 female, (U. S. Nat. Museum).
Baja California. Big Cyn., Sierra Laguna, Oct. 13, 1941, Ross and
Bohart, 2 males and 2 females, (California Acad. Sci.) ; Catavin, June 19,
1938, Michelbacher and Ross, 1 male, (California Acad. Sci.) ; Las Animas,
Sierra Laguna, Oct. 12, 1941, Ross and Bohart, 1 male and 2 females, (Cali-
fornia Acad. Sci.); Las Parras, Oct. 1925, W. M. Mann, 1 male, (U. S.
Nat. Museum); Loreto, Feb., 1923, W. M. Mann, 2 males and 3 females,
(U. S. Nat. Museum); 19 mi. E. Rosario, June 17, 1938, Michelbacher and
Ross, 3 males, (California Acad. Sci.) ; “L. Cal.”, no date, P. R. Uhler, 1
male, (U. S. Nat. Museum). Georgia. (?) Daytono, July 9, 1926, J. R.
Delano, 2 females, (Phila. Acad. Sci.). (labeled Dayton, Ga.).
\
‘
'
1
\
\
\
\
1
FIG.2 N. USINGERI N. SP.
FIG.) N. MARTINI N. SP. . FIG.3 N. MEXICANA (MELIN)
FIG.5 N. MARTINI N. SP. FIG.6 N. MEXICANA (MELIN)
FIG.4 N. STYGICA SAY
EXPLANATION OF FIGURES
Figs. 1-4, males, claspers. Figs. 5-6, females, apical abdominal sternites.
2T have not been able to locate a Dayton, Georgia, a Dayton, California, or a
Dayton, Guatemala.
116 ' THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
This species is very closely related to Nerthra mexicana (Melin)
and to N. stygica Say. It is separated from the former species by
the narow pronotum, slightly larger size, the notch of the posterior
margin of the last abdominal segment of the female being rather
pointed at the anterior end (figs. 5 and 6) and by the shape of the
clasper of the male (figs. 1 and 3). It differs from NV. stygica Say
in that it has separate hemelytra with well-developed membranes,
the emargination of the last abdominal segment of the female
slightly more pointed anteriorly, and in the shape of the male
genitalia (figs. 1 and 4).
- This species is named after Doctor C. H. Martin, who studied
the genus Gelastocoris and who collected the types located in the
Francis Huntington Snow Entomological Collection.
Nerthra usingeri Todd, new species
Size. Male: Length, 6.4 to 6.8 mm.; width of pronotum, 4.5 mm.; width
of abdomen, 4.4 to 4.5 mm. Female: Length, 7.1 to 7.7 mm.; width of pro-
notum, 4.8 to 5.0 mm.; width of abdomen, 4.7 to 5.0 mm. Color. General over-
all color yellowish-brown to dark brown nearly black. Some specimens have
the dorsal surface mottled with black and yellowish-brown. Ventrally slightly
lighter in color than on the dorsal surface; front femora are brown, darkest
basad, intermediate and hind legs yellowish-brown with dark brown rings.
Abdominal segments, both above and below have light yellowish spots at the
latero-caudal angles of each segment. Structural characteristics. Apex of
head pointedly projecting, usually with a pair of sharp-pointed tubercles,
all are variable in size. Pronotum with the lateral margins more or less
rounded, converging anteriorly and posteriroly; widest level with the trans-
verse furrow; posterior margin deeply sinuated at the middle before the
scutellum. Scutellum large, not strongly elevated. Hemelytra with well-
developed membranes, extending to or beyond the end of the abdomen;
lateral margins of the embolia nearly straight for the basal half then gently
curving medially. Connexivum visible to the width of pronotum. Bristles
very small, short, peg-like, sparsely distributed over the body. Abdominal
segments of the male asymmetrical; ninth abdominal segment small, oval,
wider than long, slightly longer than eighth segment; seventh abdominal
segment spatulate on right side, posterior margin of spatula flat. Ventral
abdominal segments of female asymmetrical; posterior margin of last
abdominal segment roundly emarginated (like N. mexicana [Melin], see
fig. 6), a moderate tumescence on the left side, a faint tumescence on the
right side of the last abdominal segment; a deep, elongate, transverse depres-
sion extending along the anterior margin of the last abdominal segment from
the median line of the abdomen to the tumescence on the left side. Clasper
of male (fig. 2), very distinctive, broad and flattened apically, widest near
apex; aedeagal furrow visible on apical half of ventral surface, terminating
before reaching apex; clasper flattened in an oblique dorso-ventral plane.
APRIL, 1954] HELFER—HIPPOMELAS 117
Holotype male, near PARKER Dam, Catirornia, April 12, 1952,
R. L. Usinger, and allotype female, wash 3.5 mi. N. Cross Roads,
California, April 12, 1952, J. D. Lattin, in the collection of the
California Academy of Sciences at San Francisco. One male and
five female paratypes, wash 3.5 mi. N. Cross Roads, California,
April 12, 1952, J. D. Lattin, in the R. L. Usinger Collection at the
University of California. One male and one female paratypes, same
data, in the personal collection of Mr. Lattin.
The difference in the locality of the holotype and the remainder
of the specimens examined is merely a difference on the part of
the two collectors in labelling the specimens. These data represent
the same locality.
Closely related to Nerthra stygica Say, N. mexicana (Melin)
and NV. martint Todd. This species may be separated from JN. stygica
by the fact that the hemelytra are normal with well-developed mem-
branes. The distinctive clasper of the male (fig 2) will separate this
species from the males of N. mexicana (Melin (fig. 3) and N.
martini Todd (fig. 1). The females of this species differ from the
females of N. martini Todd in that the emargination of the last
ventral abdominal segment is broadly rounded. To the knowledge
of the writer it may only be separated from females of N. mexicana
(Melin) by distribution.
A NEW HIPPOMELAS FROM CALIFORNIA
(Coleoptera: Buprestidae)
Jacques R. HELFER
Mendocino, California
Hippomelas dianae Helfer, new species
Holotype male elongate, subcuneate; aeneoviridis above and beneath;
pubescence short, white, moderately dense; intervals of elytra sparsely efflo-
rescent. Head moderately, coarsely, irregularly setopunctuate; eyes rather
prominent; antennae inserted under conspicuous oblique ridges, eleven seg-
mented, scape long, second segment slightly longer than broad, third segment
much longer than second, serrate from fourth segment, segments four through
eleven each with an area of sensory pores along outer edge, and with an
intero-terminal sensory fossa, terminal segment with a distinct appendix;
clypeous angularly,, not deeply emarginate; labrum bilobate, testaceous, pale.
Pronotum broadest at base with front margin broadly arcuate, sides broadly
118 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
rounded past middle becoming sinuate to basal angles which are prominent,
base narrowly sinuate at middle and more broadly sinuate at either side,
coarsely, irregularly setopunctate with a few irregular levigated spaces.
Scutellum small, rounded, depressed anteriorly. Elytra broadest at base, nar-
rowing gradually to apical third, then more strongly and becoming serrate to
apices which are bidentate, each elytron with five feeble costae; rather
densely, finely, shallowly setopunctate. Prosternal spine punctate at middle
between coxae but impunctate toward sides and tip, with a strong juxtacoxal
submarginal setopunctate stria. Mesosternum divided for reception of tip of
prosternal spine, meso-metasternal suture scarcely evident. Metacoxal plates
cut off externally by a lateral lobe of the abdomen. Abdomen with suture
between first and second segments distinct, posterior margin of third segment
strongly angulate toward sides; entire surface rather densely, shallowly,
irregularly setopunctate; last segment truncate at tip, incised at each side,
with a feeble transverse subapical plate. Forelegs with tibiae curved, strongly
margined below ,and denticulate internally, tarsi of all legs long and slender.
Genitalia dark in color, rather short, with adeagus evenly narrowed and
acute, parameres broadest at about two-thirds from their base, with margins
rather gradually curving, not lyrate. Length 13 mm., width 4 mm.
Allotype female similar in all respects except larger, length 16.5 mm.,
width 6 mm., protibiae not denticulate internally, and posterior margins of
abdominal segments two, three, and four irregularly dentate laterally. Apical
segment of abdomen largely obscured by dense efflorescence.
Holotype, allotype, and some hundreds of additional specimens,
many of them designated as paratypes, collected at Patm SprINcs
AND WHITEWATER, RIVERSIDE County, CaLirorNia, mostly in
July, by J. O. Martin, E. C. Van Dyke, P. D. Hurd, J. W. MacSwain,
and others. They were consistently taken from Ephedra. Also
several specimens from other desert localities which are doubtless
the same species but which I have not designated as paratypes.
Additional large series exist, in the collection of the University of
California at Davis, etc. Type material deposited in California
Academy of Science, principal series in California Academy of
Sciences and the California Insect Survey, University of California.
The male genitalia easily distinguish this species from Hippo-
melas planicosta and H. obliterata with which it has been confused
in collections.
Some specimens are considerably darker in color than the
types, some (fresh specimens) densely efflorescent above, some
with a faint cupreous shine. The smallest male is 11.25 mm. long,
the largest female 17.5 mm. long.
I take pleasure in dedicating this interesting species to my
wife Diane.
APRIL, 1954] FURMAN—ANDROLAELAPS 119
A NEW SPECIES OF ANDROLAELAPS FROM
PEROGNATHUS IN SOUTHERN CALIFORNIA
(Acarina: Laelaptidae)
DEANE P. FURMAN
University of California, Berkeley
The new species of mite described in this paper represents the
seventeenth species recognized in the genus Androlaelaps Berlese
1903. Of these, eight are known only from Africa (Zumpt and
Patterson 1950, Zumpt 1950), where they are found principally on
rodents of the families Muridae and Cricetidae. Two species, A.
hermaphrodita (Berl.) and A. karawaieni (Berl.), were described
from ant nests in Italy and Russia respectively, although the for-
mer species has been recorded recently by Turk (1946) from the
nest of Apodemus in Ireland. A. sardous is also known from
Apodemus in Sardinia.
A. impensus Eads 1952 is known only from a collection of bulbs
of Lilium shipped from Japan. The remaining five species of
Androlaelaps have been taken in the nearctic and neotropical
realms on rodents of the families Muridae, Cricetidae and Hetero-
myidae. The new species described here is the third one known
from hosts of the genus Perognathus.
Androlaelaps is closely related to the genus Hypoaspis Cane-
strini 1885, from which it is separable by the enlarged second pair
of legs with calcarate femora in both sexes. The chelicerae of the
female are shear-like, provided with a few teeth and a seta on the
fixed digit. The coxae are unarmed, bearing neither ventral spurs
nor stout spines. The genito-ventral plate of the female bears a
single pair of setae. In the male the holoventral plate may be fused
with or free from the anal plate. The dorsal plate is undivided.
Key TO FEMALES OF THE AMERICAN SPECIES OF ANDROLAELAPS
1. Femoral spur of leg IT with pronounced teeth. Expanded portion
of genito-ventral plate not wider than space between coxae IV Z
— Femoral spur of leg II smooth. Expanded portion of genito-
ventral plate much wider than space between coxae IV. . . a
2. Second pair of sternal plate setae overlapping bases of meta-
sternal setae. Many ventral and dorsal setae long and sinuous.
, sinuosa, Furman, new species
a Second: pair of nomial alate setae barely overlapping bases of
third sternal plate setae Body setae not long and sinuous . F
eo vet aay cy iN gpa ica gt aR as ee ET Oa eae grandiculatus Eads, 1951
3. Tarsus II with stout apical spines . . . . . Jleviculus Eads 1951
— Tarsus II without stout apical spines . . . ...... 4
120 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
4. Genito-ventral plate almost reaching anal plate. Sternal plate
with slightly concave posterior margin. ... . . setosus Fox 1946
-— Genito-ventral plate separated from anal plate by distance of
over one-half the anal plate length. Sternal plate with truncate
caudal margin . . . . . . johnstoni Eads and Hightower 1951
Androlaelaps sinuosa Furman, new species
Female.—A large mite, measuring 1.179 mm. long, exclusive of gnatho-
soma, by 0.823 mm. wide. Shape broadly oval, with slight shoulders.
Dorsal plate covering most of width of dorsum but leaving unarmed the
posterior tip of the opisthosoma; cephalic end of plate heavily solerotized
and deflexed. Thirty-five pairs of setae on dorsal plate, characteristically long
(up to 230 microns) -and sinuous.
Venter—Presternal area indistinctly reticulate. Sternal plate widened
posteriorly with concave margins measuring at narrowest points 114 microns
long by 205 microns wide, lightly reticulate; sternal setae long and sinuate,
anterior pair approximately 160 microns long arising from anterior margin of
plate, second and third pairs 230 microns in length. Metasternal and genital
setae sinuous, subequal to posterior sternal plate setae. Genito-ventral plate
gently flask shaped, small, widely separated from anal plate. Flanking the
genito-ventral plate two pairs of small narrow plates; two pairs of small
metapodal plates more laterally situated as illustrated. Anal plate with
broadly rounded anterior margin, posterior end terminating in a blunt
tip; its usual terminal position necessitates dissection in order to observe
the entire plate; adanal setae sinuous, 100 microns long; post-anal seta less
than one-half as long. Uncovered area of venter bearing approximately 10
pairs of somewhat sinuous setae. Peritremal tube with supporting sclerotized
plate extending from anterior border of coxae I almost to level of posterior
border of coxae IV with stigma located at level midway between coxae [JT
and IV; alary anterior extension of peritremal plate extends forward fusing
with anterior tip of dorsal plate. Second pair of legs greatly enlarged, cal-
carate, armed with a massive femoral spur bearing strong teeth on the inner
lateral margins; a small, blunt, striated spine located immediately distal to
large femoral spur; patella and tibia each with a striated, sharp, stout spine
bent at right angle to its axis (=lancet-shaped hair of Zumpt 1950) ; tarsus
with two prominent, stout, terminal spines and a basal spine similar to, but
smaller than, tibial spine. No other unusual features visible on legs.
Gnathosoma—typical for genus as illustrated. Capitular groove with six
transverse rows, each containing seven to ten teeth. Fixed digit of chelicera
with a short sharp seta and three teeth, movable digit bearing two teeth.
Male.—Idiosoma—1.065 mm. long by 0.823 mm. wide. Dorsum essentially
as in female.
Venter with narrow, elongate holoventral plate, which has a truncate
caudal border just posterior to hind margin of coxae IV, widely separated
EXPLANATION OF FIGURES
Androlaelaps sinuosa, female. Fig. 1. Venter; Fig. 2. Dorsal plate; Fig. 3.
Peritreme; Fig. 4. Anal plate. ‘
APRIL, 1954] FURMAN—ANDROLAELAPS 121
122 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 2
from anal plate. Genital orifice on anterior margin of holoventral plate; all
but the first of the five pairs of holoventral seate long and sinuous. Two pairs
of metapodal plates visible. Anal plate and peritreme as in female. Approxi-
mately 12 pairs of setae on unarmed portion of opisthosoma. Legs as described
for female.
Gnathosoma—Fixed digit of chelicera with subapical tooth; a short
sharp seta located at proximal level of apical four-fifths of the fixed digit.
Movable digit divided into two branches as illustrated, one opposing the fixed
digit and supplied with one tooth, the other articulated at mid-length and
produced as a long, sickle-shaped process. The usual basal brush of setae
around the movable digit present.
Holotype female and allotype male, collected 18 October, 1953;
from Perognathus sp. probably fallax fallax at Pickon Pass, Riv-
ERSIDE County, CatirorniA (Deposited in U. S. Nat. Museum).
Paratypes. Twelve females and three males with same data as type.
The following are all from Perognathus fallax fallax:
Twenty-six females, 7 males, Reche Canyon, San Bernardino County,
Calif., October 1, 1951; 16 females, 5 males, Reche Canyon, San Bernardino
County, Calif., October 4, 1951; 9 females, 6 males, Reche Canyon, San Ber-
nardino County, Calif., Oct. 5, 1951; 12 females, 2 males, Reche Canyon,
San Bernardino County, Calif., Oct. 11, 1951; 17 females, 4 males, Reche
Canyon, San Bernardino County, Calif., Oct. 12, 1951; 8 females, 4 males,
Loma Linda, San Bernardino County, Calif., July 24, 1951; 6 females, 1 male,
Loma Linda, San Bernardino County, Calif., July 27, 1951; 3 females, 2
males, Loma Linda, San Bernardino County, Calif., Aug. 2, 1951; 8 females,
8 males, Lucerne Valley, San Bernardino County, Calif., Nov. 7, 1953; 4
females, 1 male, Plunge Creek Canyon, San Bernardino County, Calif., Nov.
19, 1951.
Androlaelaps sinwosa is easily distinguished from all other
species of the genus by the presence of very long sinuous setae on
dorsal and ventral sides of both sexes. However, the most basic
morphological difference displayed by this species is the widely
divided holoventral plate of the male; all other members of the
genus have the anal plate incorporated in the holoventral plate.
Some authorities might establish a new genus for the reception
of this species. To this the author cannot subscribe, since the host
affinities and combination of morphological features definitely
align it with Androlaelaps.
Grateful appreciation is expressed to Mr. Raymond E. Ryck-
man of the Loma Linda School of Tropical and Preventive Medi-
cine, who made available the specimens described in this paper.
EXPLANATION OF FIGURES
Androlaelaps sinuosa. Fig. 5. Venter of male; Fig. 6. Male chelicera;
Fig. 7. Female chelicera.
Aprit, 1954]
FURMAN—ANDROLAELAPS
5
124. THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
REFERENCES
Eaps, R. B.
1951. New mites of the genus Androlaelaps Berlese. Journal of Para-
sitology, 37(2): 212-216.
Eaps, R. B. anp B. G. Hightower
1951. A new mite from nests of the wood rat, Neotoma micropus.
Entomological News, LXII(8) :249-252.
Fox, I.
1946. Three new mites from rats in Puerto Rico. Proceedings of the
Biological Society of Washington, 59:173-176.
Turk, F. A.
1946. Studies of Acari V, Notes on and description of new and little
known acari. Annals and Magazine of Natural History, Ser. 11,
vol. XII: 785-820.
Zumpt, F., anp P. M. Parrerson
1950. The Ethiopian species of Hypoaspis subgen. Androlaelaps Berlese
(1903), with description of a new species. South African Journal
of Medical Science, 15: 67-74.
Zumpt, F.
1950. Some remarks on the family Laelptidae (sensu Vitzthum 1943)
with descriptions of three new species from African rodents.
Parasitology, 40(3 and 4): 298-303.
THE HOST OF MYRMOSULA RUTILANS (BLAKE)
j (Hymenoptera: Tiphiidae)
During the spring of 1953, females of Myrmosula rutilans
(Blake)* were taken running about the nest sites of the andrenid
bee Nomadopsis scutellaris (Fowler)*. The association of the wasp
with the bee was so consistent that the writer suspected the wasps
of being parasitic on the bees. Females of the wasp were often
observed to enter the burrows of the bee. Final confirmation did
not come until June 15, when two females of the Myrmosula ma-
tured from cells which were taken from a Nomadopsis nest of the
previous summer. This is apparently the first host record for a
species of Myrmosula and so is of considerable interest. In fact,
it is one of the few records that we have for any wasps of the sub-
family Myrmosinae, the only other records being for Myrmosa
unicolor Say, a parasite of Tiphia sp., Halictus (Chloralictus)
pruinosm Robertson, H. (C.) stultum Cresson, and possibly Linde-
nius (Trachelosimus) columbianus errans (Fox).—Roy A. SNELL-
ING, Turlock, California.
1 Tdentification verified by P. D. Hurd, Jr.
2 Identification verified by J. G. Rozen, Jr.
AprIL, 1954] CHANDLER—ELMIDAE 125
NEW GENERA AND SPECIES OF ELMIDAE (COLEOPTERA)
FROM CALIFORNIA
Harry P. CHANDLER
California Department of Fish and Game, Red Bluff, California
The following new genera and species are described at this
time, so that they may be included in the section on the Elmidae in
a book on the aquatic insects of California soon to be published
by the University of California.
Atractelmis Chandler, new genus*
Form somewhat fusiform, length slightly more than twice width, nearly
glabrous. Head: clypeus distinct, slightly depressed; antennae moderately
long, 144 times width of head, 1l-segmented with last three segments per-
ceptably larger but not sharply differentiated; maxillary palpi (fig. 3) three-
segmented. Pronotum with sides nearly straight, converging anteriorly,
slightly convex at middle and flared basally; posterior margin not emarginate
in front of scutellum; sublateral carinae slightly divergent anteriorly, with
inner side deeply depressed ‘basally, becoming gradually less distinct to
anterior third where it disappears, connected at posterior fifth by a broad
depression paralleling the posterior margin; discal area anterior to this
depression evenly convex to anterior margin, with fine punctures; sides of
pronotum lateral to carinae very deeply punctured or rugose. Elytra widest at
anterior third; sides evenly elliptical to the rounded apices, except for slight
angulation at posterior third; humeral angles prominent, concealing margin
from above, area between them only slightly convex and continuous with
depressed base of pronotum; elytra along medial line evenly curved about 90°
from scutellum to apex, a little more strongly curved near scutellum; epi-
pleura strongly narrowed from base, narrowly tapered to fine point near base
of 5th abdominal sternite. Ventral surface with hydrofuge pile on underside
of head, hypomera, epipleura, sides of thorax, abdomen, coxae and femur.
Prosternum without short, broad anterior process under head.
Genotype: Atractelmis wawona Chandler, n. sp.
Atractelmis wawona Chandler, new species
Adult: In addition to the characters mentioned above this species may
be characterized as follows: Length 2 mm., width .9 mm.; shining black
above with four red spots on elytra. Antennae testacious to rufous at apex.
Elytra with humeral red spot nearly reaching first stria; sutural black area
widened near scutellum; subapical red spot 3 to 4 times as long as wide.
parallel to side of elytron, beginning on 5th stria and ending on 2nd; elytral
striae narrowly impressed medially, more broadly so laterally; punctures
small medially, separated by more than their own width, to coarse laterally,
1 Generic name derived from atraktos meaning spindle, referring to its fusiform
shape; and Elmis which indicated its relationships to the other genera having
-elongate sublateral-carinae and three segmented maxillary palpi.
126 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2 ©
separated by less than own width. Wings: See fig. 1. Venter piceous, medial
portion between coxae from anterior margin of prosternum to apex of 5th
abdominal segment, without tomentum, finely punctate with short, depressed
hairs from each puncture. Prosternum with posterior process margined nearly
to anterior margin, sides convergent posteriorly at about a 60° angle, roundly
truncate at apex, depressed medially behind coxae, middle coxae nearly twice
(11:6) as widely separated as hind coxae. Metasternum and first abdominal
sternite marginate laterally at beginning of hydrofuge pile. Last abdominal
segment with apex broadly rounded. Legs piceous to rufous, anterior side of
pro- and mesotibia and posterior side of meso- and metatibia with patches of
tomentum, tibia and tarsus with numerous additional long hairs; tarsi with
apex of last segment nearly as thick as tibia, claws very large and stout,
thick at base, curved 90° from base to apex. Genitalia: See fig. 2.
Holotype, male, SoutH Fork Mercep River near Wawona,
Yosemite NATIonaL Park, Catirorni, elev. 4,000 feet, 17 July
1946 (H. P. Chandler) ; paratype, male, Middle Fork, Cottonwood
Creek, Shasta County, California, 24 June 1952. The holotype will
be placed in the California Academy of Sciences, San Francisco.
The single paratype, which was dissected to study some of the
structures, will be retained in the author’s collection.
This species is amply distinct to be separated generically from
any other species known to the author. As a genus, it is related to
Cleptelmis ornata (Schaf.) and C. addenda (Fall) and Ampumixis
dispar (Fall) which have the maxillary palpi three segmented,
the epipleura tapering to a fine point posteriorly, and many other
characters of shape and sculpture. From them it can be separated
in the field by its spindle shape and the elongate posterior red
spot. Under magnification it may be separated by the shape of
the pronotum, especially the carinae not reaching the anterior
margin, and the transverse basal depression between the carinae;
and the epipleura strongly narrowed from base.
These two specimens were taken in riffle areas of a small and
a medium sized clear mountain stream. The two localities are over
two hundred miles apart, one in the Sierra Nevada mountains and
the other in the Coast Range of Northern California. This would
indicate that the species is widely distributed but quite rare, or
that little collecting has been done in the exact niche it prefers.
Rhizelmis? Chandler, new genus
Form robust, about twice as long as wide, somewhat obovate, widest near
posterior third, narrowed anteriorly to base of head, without conspicuous
convexities, strongly narrowed posteriorly to blunt apices of the elytra with
‘sides at about 70° angle, sparsely clothed with fine depressed hair above.
Head as long as wide; clypeus distinct, slightly depressed; epicranial sutures
2 Generic name derived from rhiza for root, referring to the roots and mosses
which were processed in a Berlese funnel to obtain these specimens, and Elmis.
APRIL, 1954] CHANDLER—ELMIDAE 127
depressed; antennae moderately long, 1.3 times width of head, a little longer
in male, eleven-segmented, with last three segments perceptibly larger but
not sharply differentiated: maxillary palpi three-segmented. Pronotum with
sides sinuate, converging anteriorly, slightly convex behind middle, slightly
concave anteriorly, more strongly so posteriorly; hind angles flared; posterior
margin not emerginate in front of scutellum; discal area evenly convex and
finely punctured from anterior margin to posterior fifth, broken only by fine
medial carina, bounded laterally by sublateral carinae; deep depression
extending from anterior margin posteriorly along the lateral margin to
posterior 2/5 with smaller depressions near the margin at posterior 1/5 and
at posterior 1/5 of sublateral carinae; lateral fourth coarsely and densely
punctured, with slightly depressed area along posterior margin also densely
punctured except for two small tuberosities located medially to base of
sublateral carinae; sublateral carinae nearly obscured by dense puncturing,
carinae extending from posterior margin to base of domed discal area, then
convexly around discal area nearly to anterior margin. Elytra widest near
middle; sides more strongly rounded just behind middle, then somewhat
flattened to the rounded apices; humeral angles only slightly prominent, area
between them only slightly convex and continuous with depressed base of
pronotum; elytra along medial line evenly curved about 90° from scutellum
to apex, a little less strongly curved near apex; epipleura most strongly
narrowed near the base of the metacoxa, narrowly tapered to a fine point
just beyond base of 5th abdominal segment. Venter with hydrofuge pile on
underside of head, hypomera, epipleura, sides of thorax, coxae and femora.
Prosternum with a short, broad, anterior process under head.
Figs. 1-3. Atractelmis wawona Chandler, n.g., n.sp. 1. Wing. 2. Ventral
view of male genitalia. 3. Maxillary palp.
128 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
Genotype: Rhizelmis nigra Chandler.
Rhizelmis nigra Chandler, new species
In addition to the characters mentioned above this species may
be characterized as follows:
Holotype male: length 2.6 mm., width 1.3 mm.; shining black above.
Head about as long as wide, densely covered with micropunctures and short,
depressed hairs; antennae testaceous to brown at apex. Elytra, striae nar-
rowly impressed, punctures small, separated by twice their own width, lateral
striae and punctures a little stronger, punctures separated by more than
their own width; strial intervals rugulose with scattered micropunctures.
Venter piceous, medial portion between coxae from anterior margin of thorax
to fifth abdominal segment without tomentum, but coarsely punctate and
with short, depressed hairs, except metasternum which is finely punctate and
nearly glabrous; prosternal process roughly triangular with bluntly rounded
apex, about 1.2 times as long as wide, margins raised; mesocoxae 1.4 times as
widely separated as hind coxae; metasternum with only short carinae behind
mesocoxae at the edge of the tomentous area; fifth abdominal segment emar-
ginate at apex. Legs rufotestaceous with thicker portions of femur piceous,
all tibia have at least some tomentum on both the anterior and posterior
sides. Tarsi and claws moderately enlarged. Genitalia, aedeagus evenly nar-
rowed to dorso-ventrally keeled apex; parameres narrowed from basal to
apical third then curved out and flared to obliquely truncate apex.
Allotype female: length 2.9 mm.; width 1.45 mm.; similar to type except
antennae slightly shorter, and apex of fifth abdominal segment not emar-
ginate. Genitalia, apical segment of the paired appendages three times as long
as wide and about 1/3 as long as basal segment.
Holotype, male, PARADISE CREEK, CoLusa County, CALIFORNIA,
24 July 1953, elev. 2,400 feet (H. P. Chandler). Allotype, same
data as holotype. Five paratypes same data as holotype. Holotype
and allotype will be placed in the California Academy of Science
collection, paratypes in Milton W. Sanderson’s and my own col-
lection.
The discovery of this species resulted from my attempts to
collect and associate larvae with the adults of all the genera of
Elmidae occurring in California. In the course of this work the
larvae now associated with this species were collected from two
widely separated localities. Atractelmis was the only known adult
with which no larvae had been associated. With some misgiving
the larvae were associated with Aitractelmis since they were col-
lected from similar habitats, and each had characters showing it
to belong to the Elmis section of the family. The third attempt to
‘collect adults at Paradise Creek was successful, and the correction
was made.
AprIL, 1954] CHANDLER—ELMIDAE 129
In relation to the other genera with three-segmented maxillary
palpi it is intermediate in size between Narpus which is larger, and
Cleptelmis, Ampumixis and Atractelmis which are smaller. The
sculpturing of the pronotum most closely approaches that of
Atractelmis, but the general body shape is quite different. Also
it may be separated from the latter by the projection of the pro-
sternum under the head, the shape of the epipleura and the male
genitalia with the flared tips of the parameres. The masking of the
sublateral carinae of the pronotum by the lateral punctures will
make this genus difficult to key out in a natural key unless the 3
segmented maxillary palpi, which are often difficult to count, are
used near the beginning of the key.
Larva: Length 6.2 mm.; width, prothorax .75 mm., lst abdominal seg-
ment .75 mm., 7th abdominal segment .65 mm.; long and slender with nearly
parallel sides; hemicylindrical in cross section. Eighth and ninth segments
narrowed to bluntly rounded, emarginate apex. Integument rufotestaceous
with a fuscous tinge dorsally, especially on the tubercles; tubercles small,
slightly raised, separated from each other by less than their own width except
for several glabrous patches on thorax and apical half of ninth abdominal
segment, each tubercle with a short, depressed posterior spine; hind margin
of each segment fringed with an even row of closely spaced, elongate
tubercles which appear to be bidentate posteriorly but have a short, semi-
transparent spine in socket between teeth. Head: Antennae biramous; ocelli
five, three closely placed anterior ocelli and two more widely separated
posteriorly. Prothorax with lateral, longitudinal depression connected with
transverse depression reaching nearly to medial line. Venter: Pleurae of
promeso- and metathorax divided into anterior and posterior sclerites;
anterior pleurae of prothorax separated medially by suture, sternum reduced
to a small triangular sclerite between and anterior to coxae. Procoxal cavities
open behind. Abdomen with pleurae on first to eight segments. Ninth abdomi-
nal segment twice as long as wide, emargination at apex obtuse V-shaped,
with a short projection at lateral angles; operculum 4/9 as long as segment.
Records: Paradise Creek, Colusa County, California, 21 Sept.
1952, 12 May and 24 July 1953, elev. 2,400 feet (H. P. Chandler) ;
Deep Creek, Shasta County, 12 Oct. 1952, elev. 2,200 feet (H. P.
Chandler). M. W. Sanderson noted in a letter that he had a larva
similar to one of the above sent him, from Tagoose Creek, Inyo
County, California, probably collected by Tarzwell.
This larva can be separated from those of other genera by its
general shape and the presence of pleurae on the eighth abdominal
segment. From Narpus which also has 8 abdominal pleurae, it can
be separated by its less cylindrical shape and the absence of short,
erect spines on the vertex.
130 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
The last collection from Paradise Creek consisted of 69 speci-
mens ranging from small to mature larvae. These were sorted into
4 size groups as follows: (16) 2.7 to 3 by .35 mm.; (13) 3.3 to
3.9 by .45mm.; (13) 4.5 to 5 by .6 mm.; (27) 5.5 to 6.3 by .8 mm.
This may indicate that the life cycle extends over 4 or more years.
There was also a pronounced color change between each group
from light testaceous to the black tinged mature larvae.
Optioservus canus Chandler, new species
Holotype male: Length 2.1 mm.; width .9 mm.; head, thorax and scu-
tellum black, elytra fuscous brown with testaceous humeral spots, venter
fuscous brown; entire body more or less covered with conspicuous white,
depressed hairs up to .1 mm. in length, giving grizzled appearance above and
even apparent ventrally where body is covered with hydrofuge pubescence.
Head black, alutaceous above; exposed mouthparts black, maxillary palpi
four-segmented. Antennae testaceous, 11-segmented, length equal to width of
head, basal two segments equal, distal segments 9-11 slightly flattened,
greatest width equal to that of basal segments, intermediate segments 3—8 only
2/3 as wide. Pronotum: Length .8 mm.; width 1 mm.; sides parallel basally,
arcuately convergent anteriorly, disk finely punctured, evenly convex, basal
sublateral carinae slightly divergent anteriorly, extending 1/3 of distance to
anterior margin; sides of pronotum lateral to carinae rugose, lateral margin
caniculate above and strongly arcuately depressed anteriorly. Elytra slightly
wider than prothorax, widest near middle, sides subparallel to apical third,
intrastrial and interstrial intervals micropunctate, slightly rugose and convex
except near middle of medial suture; strial punctures deep, separated by
own width or less; humeral spot reaching third striae, not sharply defined,
medial portion of elytron with poorly defined lighter brown area extending
posteriorly nearly to apex. Venter: Thorax and abdomen including hypomera,
epipleura and femur covered with hydrofuge pubescence, except medially
between coxae from head to second abdominal segment. Hypomera broad,
sides strongly convergent anteriorly; posterior prosternal process with sides
converging posteriorly, narrowly rounded apically; last abdominal segment
rounded from side to side. Legs fuscous brown with tarsi rufotestaceous,
patch of tomentum on anterior side of pro- and posterior side of meso- and
metatibia; tibia not constricted or bent near apex; last segment of tarsi not
as thick as tibia, claws moderate, curved about 90° from base to apex.
Allotype female: Length 2.5 mm.; width 1.4 mm. Similar to male except
antennae shorter, only 4/5 width of head. Elytra with humeral spot less
distinct, interstrial intervals more uniformly convex.
Holotype, CHALONE CREEK, PiInNACLES NaTIonAL MONUMENT,
San Benito County, Carirornta, elev. 1,000 feet, 3 May 1946
(H. P. Chandler). Allotype same data. Paratypes; 1¢ and 1 9
same data as type; 19°? Santa Barbara and vicinity, California,
(F. E. Winters) ; 1 9 Riverside, California (F. E. Winters). Holo-
type and allotype will be placed in California Academy of Sci-
APRIL, 1954] FENDER—MALTHODES 131
ences; one paratype in the collection of M. W. Sanderson and the
rest in the author’s collection.
This species is probably most closely related to O. divergens
(LeConte) from which it can be separated by having the hairs of
the body half again as long and more conspicuous, giving a
grizzled appearance; the elytra brown with a humeral spot, in-
stead of solid black, and strial intervals more convex. In addition
to some of the above characters, it may be distinguished from O.
quadrimaculatus (Horn) by having smaller poorly defined humeral
and (if present as in the paratype from Santa Barbara) subapical
pale areas which are more yellow than red.
ON SOME MALTHODES
(Coleoptera: Cantharidae)
KENNETH M. FENDER
McMinnville, Oregon
MALTHODES COLUMBIENSIS Fender
Due to a typographical lapsus, ten paratypes were omitted from
the original description of this species. These have been distributed
as paratypes and as such should be considered. They were all col-
lected by G. Stace Smith at Creston, B. C. on the following dates:
May 5, 1947 (2), May 7, 1947 (1), May 14, 1948 (3), May 15,
1948 (1), May 21, 1948 (1) and May 25, 1948 (2).
Malthodes stacesmithi Fender, new species
Black, mandibles and posterior margin of the pronotum nar-
rowly obscurely paler, elytra beyond the basal fifth, tarsi and the
apices of the tibiae piceous, male last dorsals, seventh ventral and
median portion of the sixth ventral flavous, pubescence cinereous,
inconspicuous, fine and sparse. Length 4 mm.
Male. Head wider than the pronotum, finely sparsely punctured behind
the eyes which are large and prominent, antennae broken off beyond the ©
eighth segment in the type, second and third segments equal, the fourth
slightly longer, the intermediate segments about three times as long as wide;
pronotum shining, transverse, the anterior angles obliquely rounded, the
sides nearly straight and parellel to the hind angles which are rounded, disc
very finely sparsely punctured, a small triangular impression medially at
the base; elytra extending to the apex of the fifth ventral segment, sparsely
punctured basally, becoming rugose apically, the apices not appreciably
tumid.
132 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
y
——_
EXLANATION OF FIGURES
Fig. 1. male terminalia of Malthodes stacesmithi, ventral view. Fig .2.
Same, lateral view.
Female. Similar to the male, head narrower than the pronotum, the eyes
small, antennae missing beyond the second segment in the allotype; sides of
the pronotum straight, converging slightly to the rounded hind angles;
elytra extending to the apex of the fourth ventral segment; seventh ventral
acutely triangularly notched.
Male terminalia: Ventral view (Fig. 1); sixth ventral deeply emar-
ginate, the base of the emargination truncate, seventh ventral elongate,
extending beyond the sixth by about one and a third times the length of the
sixth, forked at the apical third, the forks strongly divergent, becoming
parallel apically, the tips rounded, apices of the side pieces of the penul-
timate dorsal subtriangular. Lateral view (Fig. 2); sixth ventral obovate,
seventh ventral slender, evenly sinuately ascending, the tip rounded; last
dorsals somewhat arched; sides of penultimate dorsal descending, obliquely
doubly folded, the folded section slightly projected at the posterior angles
into podiform processes; the last dorsal concealed.
Holotype, male, BARKERVILLE, British CoLumBia, August 12,
1950, collected by G. Stace Smith; allotype, female, same data as
‘male type but collected August 14, 1950. Types in the Stace Smith
collection.
This species falls in my group X and in the key to that group
would run to Malthodes furcifer LeConte. The penultimate dorsal
is more rudimentary than in M. furcifer as indicated by the sides
being merely folded rather than partially abbreviated basally as in
M. furcifer. The basal pronotal margin is narrowly pale in M.
stacesmithi whereas the pronotal disc of M. furcifer has a small
pale spot medially on each side.
Aprit, 1954] TIMBERLAKE—NOMADA 133
TWO NEW SPECIES OF NOMADA, SUBGENUS GNATHIAS,
FROM CALIFORNIA’
(Hymenoptera: Apoidea)
P. H. TimBerLake
University of California Citrus Experiment Station, Riverside
Up to the present time no species of Gnathias has been described
or recorded from California, except that Fowler, in 1899, recorded
what is apparently a single species of the group as lepida (¢) and
bisignata (2), both names having been incorrectly applied. There
are, however, several species of Gnathias resident in California,
and by request I am now describing two new species to eve
names for the recording of biological data.
Nomada (Gnathias) opacella Timberlake, new species
N. lepida Fowler, 1899, Ent. News, 10, pp. 159, 161, @ (not Cresson).
N. bisignata Fowler, 1899, Ibid., pp. 159, 162, 2 (not Say).
This is a small Gnathias, which differs from similar eastern
species in having the abdomen comparatively dullish, with a fine
obscure puncturation, and from several other western species of
similar dullish aspect in having the apical depression of the tergites
comparatively broad, wude, and punctureless, and in having dis-
tinct yellow maculae on the second tergite. The male differs from
N. lepida Cresson in the entirely black scape, in the more infus-
cated legs and abdomen, and in having antennal joint 4 much
longer than 3.
Female—Dark-reddish ferruginous, with black markings on head and
thorax. Basal and lateral margins of labrum more or less yellow. Entire pos-
terior surface of head black, except rather narrow orbital stripes that unite
with a transverse band across the vertex; a large quadrate black area on face,
extending from antennae to ocellar region, enclosed by red orbital stripes
which have an inward-directed spur before the summit of the eyes by which
the black is notched on each side, the black area usually enclosing a small red
patch in front of anterior ocellus. Sutures from antennal sockets to clypeus |
more or less black. Mesoscutum with four red and three black stripes that are
nearly equal; the lateral margins in front of tegulae also narrowly black.
Sternum and sides of prothorax, area of mesopleura just beneath wings and
behind tubercles, metapleura and contiguous margin of propodeum, and
median stripe on propodeum, black. Red mark on pleura generally large and
extending across the posterior part of mesosternum. Abdomen dark red, more
or less coppery on apical depression of tergites; the base of tergite 1 broadly
black, as is the concealed base of following tergites, which thus imparts a
duskiness to the coloration. On each side of tergite 2 a rather small, pale-
yellow spot; sometimes a pair of smaller spots on tergite 3. Antennae dark
, Paper No. 799, University of California Citrus Experiment Station, Riverside,
California,
134 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
ferruginous, with the scape black above except toward base, and the flagellum
infuscated above. Legs dark red; the coxae, except more or less at apex or
on anterior side, mark at base of front and middle femora beneath, hind
femora more or less on anterior and posterior sides, and hind tarsi except
toward apex, black. Tegulae ferruginous. Wings smoky except for the usual
clear spot beyond the submarginal and discal cells. Nervures fuscous, the
stigma dull ferruginous.
Head and thorax with the usual dense, coarse puncturation; abdomen
dullish; the base of tergites 2 and 3 very minutely and densely punctate,
the apical depression of tergites broad, nude, and impunctate. Apex of
pygidial plate rounded, sometimes slightly truncate. Scutellum weakly bi-
lobate. Antennae moderately elongate, the middle joints of flagellum about
one and one-half times longer than thick; joint 3 on short side a little more
than half as long as joint 4. Apex of hind tibiae opposite spurs armed with one
long, slender bristle and three progressively shorter, coarse, curved black
bristles. Second and third submarginal cells broad below, the third about
half as wide as the second above. Pubescence white, becoming more or less
yellowish above, with long, coarse, dusky bristles intermixed on face and
scape of antennae. Apical felt band of tergite 5 narrow and white. Length,
6.5-7 mm.; anterior wing, 5.5—6.1 mm.
Male—Head and thorax black. Mandibles except tips, labrum, clypeus
except upper margin of disc, lateral marks slender above and reaching level
of antennae, and sometimes a short postorbital line (generally restricted to
small spot next to base of mandibles), lemon yellow. Thorax entirely black,
or tubercles more or less reddish, and more rarely a small yellow spot on
anterior part of pleura. Abdomen dull ferruginous, black and yellow; basal
half of tergite 1 black, and a broad black band at the base of tergites 2 to
6 often appearing like an apical or preapical band on the preceding segment;
a yellow band on tergites 1 to 6 usually narrowly interrupted on 1, broadly
interrupted on 2 and 3, and sometimes more or less interrupted on 4; the
yellow on tergites 2 to 6 with a more or less distinct posterior emargination
on each side by intrusion of the darker ground color, these intrusions
represented on tergite 1 generally by a small black, oval or roundish spot on
each side; apical depression of tergites and area between the interrupted
parts of bands, ferruginous. Venter with broad yellow bands. Scape of
antennae entirely black; flagellum black above, more narowly toward apex,
and dull ferruginous beneath. Legs black behind, rather narrowly so on front
trochanters, femora, and tibiae, the hind femora dark except on upper an-
terior side, and the hind tibae dark except on inner side; legs otherwise
ferruginous, more or less washed with yellow, especially on anterior side of
front femora and tibiae, anterior side of middle femora, and at apex of the
light part of hind femora and of the middle and hind tibiae; hind tarsi dark,
the front pair ferruginous tinged with brown on outer side, and the middle
intermediate in color. Tegulae dark ferruginous. Wings nearly as in female.
Inner orbits of eyes distinctly converging below. Antennae moderately
elongate, the scape moderately swollen; joint 4 a little longer than 13 and
somewhat less than twice as long as 3; joints 5 to 12 rather strongly sinuate
and denticulate on outer margin beneath. Tergite 7 distinctly notched at apex.
Length, 5.5-9 mm.; anterior wing, 4.5-6.5 mm.
APRIL, 1954] TIMBERLAKE—-NOMADA 135
Variation: Rarely, the yellow marks on tergite 1 reduced to small spots or
the marks on tergites 1 to 4 all reduced to small lateral spots; conversely and
more rarely, the yellow markings may form wide bands, very narrowly in-
terrupted on tergite 1, incompletely interrupted on tergite 2, and entire on
following segments.
Holotype female and allotype, male, BERKELEY, CALIFORNIA,
on Ranunculus californicus, March 17, 1941 (E. G. Linsley).
The types and following paratypes in collection of Citrus Expe-
riment Station, Riverside: 2 females, 27 males taken with the
types; 1 male, Berkeley hills, March 4, 1932 (Margaret L. Cook) ;
1 male, 1 female, Visalia, March 29 and April 21, 1939 (F. T.
Scott) ; 2 females, Pine Flat, near California Hot Springs, flying
over ground, May 3, 1947 (Timberlake) ; and 1 female, Laguna
Mountains, San Diego County, May 17, 1948 (Crickmer). Para-
types in University of California collection, Berkeley, as follows:
1 female, Orinda, Contra Costa County, on Ranunculus, March 21,
1946 (R. Smith and MacSwain); 1 male, Berkeley, March 16,
1939; and 5 females, 42 males, Berkeley (J. W. MacSwain), col-
lected April 15 and 19, 1946; March 11, 13, 16, 1947, and March
21, 25, 26 and April 3, 1952.
Nomada (Gnathias) debilis Timberlake, new species
Allied to opacella, with which it agrees closely in sculpture, but
smaller and having antennae of both sexes considerably shorter.
Female—Clear dark ferruginous ,with the following black markings:
a dot in suture on each side of clypeus; mark between and extending a little
above antennal sockets; transverse mark covering ocelli; large area on
occiput (leaving genae broadly red); prosternum and mark on sides of
pronotum; median stripe on mesoscutum (and sometimes a short stripe on
each side) ; small spot on middle of propodeum; depressed areas below and
behind wings; metapleura more or less and contiguous anterior margin of
sides of propodeum, with an extension to area between middle and hind coxae
on each side; base of front coxae, middle coxae except apex, and posterior
side of hind coxae except apex. Hind femora slightly infuscated beneath, and
hind basitarsi more or less fuscous on outer side. Antennae uniformly light
ferruginous. Mandibles rufous at apex. Abdomen clear ferruginous, with
extreme base of tergite 1 slightly blackened. A small yellow spot on each
side of tergite 2, and sometimes traces of lateral spots on tergite 3. Tegulae
end wings as in opacella, except that the stigma is more infuscated.
Structure, sculpture, and pubescence about as in opacella, but head more
transverse and antennae considerably shorter, with joint 3 three-fourths to
four-fifths as long as 4, and the middle joints of flagellum not more than
one and one-third times longer than thick. Length, 5-6.5 mm.; anterior
wing, 4.5-5 m..
Male—Head and thorax black. Genae at anterior end of eyes, mandibles
except reddish tips, labrum, and broad band across anterior border of face,
136 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
extending very narowly upward on orbits to level of antennae, pale yellow
(the black of face more or less evenly truncate anteriorly and covering base
of clypeus). Two red spots on scutellum, sometimes enlarged and confluent,
and sometimes a small red spot on each side of hind margin of pronotum.
Tubercles ferruginous or yellow or tipped with yellow, and a small yellowish
mark on anterior border of the sternopleural region of mesothorax on each
side. Abdomen clear ferruginous, except that the base of tergites 2 to 7 is
black, imparting a duskiness to the overlying portion of preceding segment,
and nearly the basal half of tergite 1 is black. A moderately large, nearly
circular yellow mark on each side of tergite 2, smaller marks on tergite 3, and
usually a small yellow spot on each side of tergite 4. Legs ferruginous, but
the coxae almost entirely, posterior side of trochanters and of hind femora,
under margin of front and middle femora and outer side of hind basitarsi,
black; front and middle tibiae a little infuscated behind. Antennae fer-
ruginous, but scape black, either entirely or often with a yellow or reddish
stripe beneath; first four joints of flagellum broadly, and the following joint
to apex narrowly, black above. Tegulae and wings as in female.
Other characters about as in male of opacella, except that the antennae
are considerable shorter; antennal joint 4 equal to 13, and joint 3 on its
short side about two-thirds as long as 4; middle joints of flagellum about
one and one-third times longer than thick. Length, 5-6.5 mm.; anterior
wing, 4.5-5 mm.
Holotype female and allotype, TeETLEY Park, SEELEY FLAT, SAN
BERNARDINNO Mrts., CaLirornia, about 4,500 feet, at flowers of ap-
ple, May 15, 1937 (Timberlake). Paratypes as follows: 12 fe-
males, on Potentilla glandulosa, May 13, 1934; 3 females on same
flowers, May 23, 1936; 2 females on Ceanothus integerrimus, May
16, 1936; 1 female, 13 males at flowers of apple, 1 male on Salix
laevigata, 2 males on Montia perfoliata, and 8 males on Nemophila
integrifolia, May 15, 1937; 2 males flying over ground and 3 males
on Nemophila integrifolia, May 8, 1940 (Timberlake) ; and 1 fe-
male, May 8, 1940 (C. M. Dammers), all at type locality; 1 male,
Mill Creek, San Bernardino Mountains, 6,000 feet, on Ceanothus
cordulatus, May 20, 1946; and 1 male same locality, on Arctosta-
phylos patula, May 16, 1948 (Timberlake). Types in collection of
Citrus Experiment Station, Riverside.
Var. a. — Female with black markings nearly extensive as in opacella,
with the red forming a band across upper part of frons; the legs and abdomen
clear red, but the black forming three stripes on mesoscutum; a median stripe
or propodeum, and a broad oblique band from hind wings to middle and hind
coxael (Sierra Nevadas). 1 female, Miami Ranger Station, Mariposa County,
June 4 and 7, 1942 (E. G. Linsley) ; and 1 female, Oakhurst, Madera County,
on Ceanothus, June 5, 1942 (Arthur J. Walz).
APRIL, 1954] WIRTH—TABANOIDEA Atow?e
A NEW SPECIES OF GLUTOPS AND OTHER NEW RECORDS
OF CALIFORNIA TABANOIDEA
(Diptera)
Wits W. WirTH
Entomology Research Branch, Agricultural Research Service
U. S. Department of Agriculture
Through the courtesy of Dr. Paul D. Hurd, Jr., I have had the
pleasure of examining a collection of Rhagionidae and the related
families Erinnidae and Coenomyiidae from the California Insect
Survey at Berkeley. In all 30 species and 540 specimens were rep-
resented. The most important records are presented here, together
with a few distributional and descriptive notes. I am also greatly
indebted to Dr. Frank R. Cole of Redlands, California, for the
opportunity to study some specimens from his collection of the
very rare genus Glutops, including a new species here described.
Mr. Alexander A. Hubert of Hamilton, Montana, gave me the
benefits of his intensive study of Symphoromyia on points of
synonymy just as this paper was going to press. I also wish to
thank Dr. L. L. Pechuman of Lockport, New York for his critical
comparisons, loans of specimens, and other valuable assistance.
FAMILY COENOMYIIDAE
Genus GLuTops BurGEss
Glutops Burgess, 1878, Proc. Boston Soc. Nat.. Hist., 19: 321 (Genotype:
Glutops singularis Burgess, monobasic).
The genus Glutops has interested dipterists generally because
specimens are rare in collections, and because the face has on each
side a peculiar bulbous prominence which is especially swollen and
covered with long hairs in the males. Only two species have pre-
viously been known, each from only a few specimens. One of these
species was represented in the California material examined, as
well as a third undescribed species.
GLuTops Rossi Pechuman
Glutops rossi Pechuman, 1945, Canad. Ent., 77: 134.
This species has previously been known only from British
Columbia (type locality: Port Haney) and Montana: I have ex-
amined the following specimens from California:
1 2 Pine Creek, Modoc County, July 18, 1948, W. W. Wirth (el. 7000
ft.) (in U. S. National Museum); 1 ¢, Point Reyes, Marin County, June 5,
1949, R. E. Ryckman (U.S. N. M.); 1 2, Lone Pine, Inyo County, July 28,
1940, L. J. Lipovsky (Kansas Univ. collection); 1 @, Mt. Home Canyon,
June 8, F. R. Cole (Cole collection).
138 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
Glutops punctata Wirth, new species
Female. Length 10 mm., wing 10.4 mm. by 2.6 mm.
Head pearly gray pollinose; frons 0.43 times as broad as greatest width
of head across eyes in dorsal view; ocellar triangle about equilateral, on a
very prominent tubercle, the distance from the anterior ocellus to bases of
antennae about 0.4 of width of frons. Facial prominences not quite as strong
as in G. singularis Burgess, with much denser, coarser, black hair. Palpi
orange yellow, nearly as long as antennae, apices abruptly bent downwards,
each with a flattened, bare dorsal area, and not broader than basal portions.
Labium brownish and expanded in a distally flattened, ovoid disc apparently
suitable for use as a suction cup in feeding. Antennae with first and second
segments pruinose buff-colored, with numerous long, stout, black hairs;
combined lengths of first two segments 0.7 of length of third segment. Third
segment with nine indistinct annuli, basal annulus concolorus with preced-
ing segments, second to fifth bright orange, very little broader than basal
segments, sixth and succeeding annuli jet black and slender. Thorax pruinose
gray, appearing mottled due to minute black punctations at bases of the
numerous, strong, black hairs over all surfaces. Three very narrow, indis-
tinct, black, longitudinal vittae on dorsum. Legs reddish brown, coxae with
dense, dark gray pollen. Legs with very short black hairs except those on
coxae, those in a ventral tuft at apex of each fore trochanter, and those on
posteroventral surface of all femora, which are long. Wings with membrane
reddish hrown infumated, the veins very little darker. Halteres with yellowish
stems, grayish brown knobs. Abdomen pearly gray pollinose, with vestiture
of coarse black hairs, each hair with a strong, rounded, black spot at base,
these spots usually broader than the distances across the intervening gray
ground color between them. Base of third tergite with a mesal row of about
fifteen small, oval, polished black sensory pits in a transverse depression,
posterior tergites and sternites each with a few scattered pairs of similar
sensoria as in the genotype. Sixth and succeeding segments greatly com-
pressed and telescoped and yellowish brown in color.
Male. Specimen badly damaged, third antennal segments and abdomen
missing. As in the female with the usual sexual differences, the most striking
consisting of the enormously swollen facial prominences and the greater
length of the body hairs, the facial prominences and scutellum appearing
especially hirsute, but not nearly so much as in G. singularis. Eyes broadly
contiguous above. Mesonotum darker slate-colored gray, the vittae very faint.
Wing 10.0 mm. by 2.3 mm.
Wirth, new species
Holotype 9, FALLEN Lear Lake, Lake TaHOE, CALIFORNIA,
July 2, 1915, E. C. Van Dyke (deposited in the California Academy
of Sciences). Allotype, Agassiz, British Columbia, June, 1915,
R. C. Treherne (F. R. Cole collection). Paratypess 1 9, Homestead
Inn, Mt. Hood, Oregon, June 30, 1927, E. C. Van Dyke (deposited
in U. S. National Museum) ; 1 9, Trinity County, California, May
27, 1934, T. G. H. Aitken (California Insect Survey collection) ;
APRIL, 1954] WIRTH—TABANOIDEA 139
1 §, Yeomatt, Washington, June 3, 1929, V. Tartar (C. E. Philip
collection).
The Agassiz, British Columbia, specimen was originally re-
ported by Gibson (1916, 47th Ann. Rept. Ent. Soc. Ontario, p. 154)
as G. singularis: Burgess, but Pechuman (l.c.) not being able to
locate the specimen, was naturally inclined to believe that it
probably referred to his western species G. rosst. GC. singularis has
been recorded only from the northeastern states of New Hampshire,
Massachusetts, Connecticut, New York and Pennsylvania. | am
indebted greatly to Dr. Pechuman, to Dr. Marion E. Smith of the
University of Massachusetts, and to Dr. C. H. Curran of the Ameri-
can Museum of Natural History for the loan of five female speci-
mens of G. singularis for comparison with my western species,
thus enabling me to study both sexes of each of the three species
together. I am therefore able to present the following key for their
separation:
Key TO THE SPECIES OF GLUTOPS
1. Antennae and legs black, halter knobs whitish, mesonotum with broad,
dark gray vittae; wings with veins dark colored; length about 6 mm.
eas NIA, Beha dedket Crate entre a meter SAL EY Pinel A seni eee rosst Pechuman
— Antennae yellowish to orange at bases, only extreme apices black; legs
reddish brown; halter knobs infuscated; mesonotum with narrow dark
brown or black vittae; length 8-10 mom...wn.n... eon eee eeeeececeeeeeeceeceeees 2
2. Body hairs coarse, each arising from a round black dot; wing membrane
dark brown, concolorous with borders of veins; mesonotal vittae black;
antennae with first two segments combined half as long as third segment,
the latter not swollen in middle; ocellar triangle equilateral; length
EQ venir’ 88s Sire zeae te CEN MN ea tern ee Naa DI Bans | punctata Wirth
— Body hairs fine, not arising from black dots, the body rather uniformly
pollinose gray; wing membrane pale, contrasting strongly with dark
brown-bordered veins; mesotonal vittae brown; antennae with first two
segments combined over two-thirds as long as third segment, the latter
considerably swollen in middle; ocellar triangle longer than broad;
VEN etH yO ales ts cnr ee oe Pek cee eee ie a ea ae singularis Burgess
FAMILY RHAGIONIDAE
GENUS VERMILEO MAcQuaRT
VERMILEO OPACcusS (Coquillett)
Vermileo opacus (Coquillett), 1904. Inv. Pac. 1:21 (Pheneus); Swezy, 1929,
Proc. Hawn. Ent. Soc. 7:231; Leonard, 1930, Amer. Ent. Soc. Mem.
7:32; Pechuman, 1938, Bull. Brooklyn Ent. Soc. 33:84.
Coquillett described V. opacus from a male from Ormsby
County, Nevada; Leonard added a record from Alamogordo, New
Mexico; and Pechuman described the female from Pasadena, Cali-
ov" THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
fornia and added a record from Zion Canyon, Utah. In the U. S.
National Museum there is a female of V. opacus collected at
Yosemite, California, at 3000 feet altitude by W. M. Wheeler which
had been determined by him as V. comstocki. I have also seen a
male and female from the Calfornia Insect Survey, taken at Snow-
line Camp, Eldorado County, California, July 22, 1948, by J. W.
MacSwain. —
VERMILEO COMSTOCKI Wheeler
Vermileo comstocki Wheeler, 1918, Proc. N. England Zool. Club 6:83;
Greene, 1926, Proc. U. S. Nat. Mus. 70:12; Leonard, 1930, Amer. Ent.
Soc. Mem. 7:71; Leonard, 1931, Trans. Amer. Ent. Soc. 57:323; Pechu-
man, 1938, Bull. Brooklyn Ent. Soc. 33:87.
Wheeler collected his type series of V. comstocki at Alta
Meadow, near Sequoia National Forest, California, elevation 9000
feet. Pechuman gives the location of the holotype as the Museum
of Comparative Zoology at Cambridge, Massachusetts; there are
five specimens labelled as cotypes in the U. S. National Museum.
I have also examined 1 male, Sentinel Dome, California, June 19,
1938, E. O. Essig, elevation 8117 feet (California Insect Survey),
1 female, same data (U.S.N.M.), and 1 female, Strawberry, Tuol-
umne County, California, July 15, 1951, J. W. MacSwain (C.1.S.).
All the known localities for V. opacus are at an elevation indicating
an Upper Sonoran distribution, while the V. comstocki localities
are Transition or above.
GENUS SYMPHOROMYIA FRAUENFELD
This genus is especially important as it contains the only blood-
sucking members of the family Rhagionidae in North America. In
the mountains of the northern and western parts of the country
these biting snipe flies are as annoying and painful biters as mem-
bers of the Tabanidae. Aldrich’s (1915, Proc. U. S. Nat. Mus.
49:113-142) revision of the North American species still stands
as the authoritative work and although excellent, badly needs to be
brought up to date with a study of the male genialia. Species re-
ported by Aldrich to take blood include atripes Bigot, flavipalpis
Adams, hirta Johnson, inquisitor Aldrich, pachyceras Williston
and possibly kincaidi Aldrich. I captured a female of sackeni
Aldrich (near Saratoga, Santa Clara County, California, July 8,
1948) in the act of biting painfully.
I have identified the following California species of Sympho-
romyta in the California Insect Survey collection.
1. atripes Bigot. 78 99, Echo Lake, Eldorado County; Delany Creek,
APRIL, 1954] WIRTH—TABANOIDEA 7 141
10.
Th
Yosemite; White Mountain, Inyo County: Gaylor Lakes, Yosemite:
Hope Valley, Alpine County; Young Lakes, Yosemite.
. fulvipes Bigot. 34 9 9, Hat Lake, Lassen County; Donner Pass, Nevada
County; North Park, Mirror Lake, Young Lakes, Yosemite; Echo Lake,
Eldorado County; Hope Valley, Alpine County; Buck’s Lake, Plumas
County; Mt. Raymond, Madera County; Tuolumne Meadows, Tuol-
umne County; Dark Creek, Tahquitz Valley, Idyllwild, San Jacinto
Mountains. [I believe that flavipalpis Adams from Utah, which appar-
ently differs mostly in its darker femora, will eventually prove to be a
synonym of fulvipes, while hirta Johnson, with a much narrower frons
and broad mesotonal bands should be restricted to the eastern form.
All of Aldrich’s Rocky Mountain records of hirta should be transferred
to flavipalpis].
. johnsoni Coquillet. 2 ¢ 8, 25 2 2, Keen Camp and Pine Grove, San
Jacinto Mountains; Echo Lake, G. Alpine Creek, Lake Forest, Tahoe;
Spaulding’s, Lassen County; Buck’s Lake, Plumas County; Miami
Ranger Station, Mariposa County.
kincaidi Aldrich. 1 9, Mirror Lake, Yosemite, July 20, 1936, W. G.
Herms.
. limata Coquillet. 108 2 2, Idyllwild, Ribbonwood, Keen Camp, Pine
- Grove, Santa Rosa Mountain, Herkey Creek, San Jacinto River, San
Jacinto Mountains; Tanbark Flat, Camp Baldy, Van Nuys, Pasadena,
Los Angeles County; Poppet Flat, Riverside County; Hastings Refuge,
Monterey County; Portola State Park, San Mateo County.
. montana Aldrich. 22 64,3 2 9, Hope Valley, Alpine County; Bridge
Creek Camp, Lassen County; Triple Peak Fork, Yosemite; Sardine
Creek, Mono County.
. pachyceras Williston. 4 ¢ 6, 23 992, Mt. Hamilton and San Antonio
Valley, Santa Clara County; Cypress Ridge, Lagunitas Creek, Marin
County; Sunol, Alameda County; Ryan Creek, Mendocino County; Hat
Creek, Shasta County; Echo Lake, Eldorado County; Young Lakes,
Yosemite.
. plagens Williston. 4 6,6 2 9, Trinity County; Donner Pass, Nevada
County; Green Valley Park, Solano County; China Flat, Echo Lake,
Eldorado County; Strawberry, Tuolumne County; Mt. Raymond, Madera
County; Frazier Mt., Kern County.
. sackeni Aldrich. 5 6 6, 92 9 2, Pine Grove, San Jacinto River, Idyll-
wild, Dark Creek, San Jacinto Mountains; Tanbark Flat, Big Dalton
Dam, Pasadena, Los Angeles County; Loma Prieta, Santa Clara County;
Frazier Mountain, Kern County; Davis, Yolo County; Pepperwood,
Scotia, Yosemite.
securifera Coquillett. (see below 13 @ @ ).
varicornis (Loew). 4 92, Phoenix Lake, Taylor State Park, Marin
County; Oak Grove, San Diego County.
Of the above listed species, Aldrich did not include California
records of fulvipes and montana, and the present records are thus
apparently new for the state. However, Aldrich listed the following
142 THE PAN-PACIFIC ENTUMOLOGIST [VOL. xxx, NO. 2
species from California, cinerea Johnson, cruenta Coquillett, pilosa
Aldrich and trucis Coquillett, which I did not find in the Survey
collection. 2
SYMPHOROMYIA SECURIFERA coquillett
Symphoromyia securifera Coquillett, 1904, Proc. Ent. Soc. Wash. 6:171;
Aldrich, 1915, Proc. U. S. Nat. Mus. 49:140.
SPECIMENS EXAMINED: 12 99, Tanbark Flat, Los Angeles Coun-
ty, California, June 20, 1950, J. W. MacSwain; 2 99, same locality,
June 20 and 25, 1950, P. D. Hurd (in collections of U.S.N.M.
and California Insect Survey).
Aldrich’s description of securifera from a female collected by
Osten Sacken in Sonoma County, California, differs so much from
the type female described by Coquillett from Santa Clara County,
that I believe it advisable to redescribe the species again based
on fresh material. The type agrees with these Tanbark Flat speci-
mens except that the legs are, as described by Aldrich, mostly
yellow. Aldrich’s figure 11?, allegedly of the mid coxa of securifera,
is referred by him in his later notes to johnsoni. This clump of
modified black spines on the outer side of the mid coxa is found,
as stated earlier in Aldrich’s paper (p. 114) in males of several
species in the group with a concave third antennal segment.
Female. Length 5.7 mm. Front half as wide as one eye, densely gray
pollinose, with rather long, coarse, black pile; slightly bulging on each side
below ocellar triangle, the latter on prominent elevation. First antennal seg-
ment pollinose gray, short and slightly swollen, with coarse black pile;
second segment less than a fourth as long as first; third segment pubescent
black, concave below the black arista, much elongated below, its length
equal to length of entire antenna to base of arista. Face bare, grayish-white
pollinose; palpi orange-yellow, broad beyond middle, with whitish pile;
labellae fleshy, blackish; beard white.
Mesonotum densely gray pollinose, with coarse black pile rather short
except long in front of scutellum; with three very marked brownish-black
longitudinal vittae, the median vitta very narrow, the gray areas between this
and lateral vittae subequal in breadth to that of the latter. Scutellum gray,
with long black pile; pleura finely gray pollinose, with very fine whitish
pile, propleura and metapleura with dense long white pile. Legs black;
coxae gray pollinose, with dense white pile, mid coxae without spine-like
clump of bristles; femora with very fine, short, white pile mixed with black
pile on fore legs; fore and mid knees yellowish; fore and mid tibiae brown-
ish; tarsi black. Wings grayish hylaine, veins dark brown, becoming yellow-
ish at base of wing. Haltereas entirely yellow. Abdomen densely gray polli-
nose, tergites each with a rather elongated, median, brownish spot, those on
posterior segments usually somewhat broader and less distinct; pile on first
tergite and on venter white, on distal tergites black and coarse.
2 Likewise Aldrich’s figures 4 and 5, p. 130, should refer to sackeni Aldrich, and
not, as labeled, to kincaidi Aldrich.
APRIL, 1954] SLATER & KNIGHT—HEMIPTERA 143
THE TAXONOMIC STATUS OF OLIGOTYLUS VAN DUZEE
AND LEPTOTYLUS VAN DUZEE, WITH THE DESCRIPTION
OF A NEW SPECIES OF PSALLUS
James A. SLATER! AND Harry H. Knicur?
E. P. Van Duzee (1916) in his synoptic keys to the genera of
North American Miridae described three new genera of the sub-
family Phylinae for which no species were included. These genera
were Strophopoda, Oligotylus and Leptotylus. Van Duzee assumed
that these generic names were invalid in the above mentioned paper
and noted that he intended to validate them later by the publica-
tion of included species. He did this, however, only in the case of
Strophopoda® by the description in 1921 of Strophopoda aprica.
This species becomes the type species of Strophopoda by subse-
quent designation. In the cases of Leptotylus and Oligotylus, no
species have been included in these genera. Opinion 46 of the
International Rules of Zoological Nomenclature establishes the
principal that genera described without the inclusion of any species
are valid. Leptotylus and Oligotylus therefore must be considered
validly establish genera. It seems essential that type species be
assigned to these generic names so that a type species inadver-
tently or accidentally assigned may not cause the synonymy of well
known generic names proposed subsequent to 1916.
Dr. E. S. Ross of the California Academy of Sciences has kindly
checked the Van Duzee collection of Miridae in an attempt to
locate specimens bearing labels of either of these genera. Five
specimens under the name Oligotylus have been located and prove
to pertain to a new species of Psallus described below. We hereby
designate as type species of Oligotylus Van Duzee, Psallus brevi-
tylus new species. Oligotylus Van Duzee 1916 is therefore a junior
synonym of Psallus Fieber 1858.
In the case of Leptotylus, no specimens under this name appear
to be present in the Van Duzee collections. The type species of
Lepitotylus Van Duzee is here designated as Microphylellus longi-
rostris Knight. This is a species that agrees in all essentials with
the generic description of Leptotylus. Leptotylus Van Duzee 1916
is therefore a junior synonym of Microphylellus Reuter 1909.
1 Department of Zoology and Entomology, University of Connecticut, Storrs.
2 Department of Zoology and Entomolegy, Iowa State College, Ames.
3 Carvalho (1952) dates Strophopoda from 1921, but as noted above the genus ~
should actually date from 1916.
144 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
Psallus brevitylus Slater and Knight, new species
General coloration black, second antennal segment and extreme
apex of first segment light tan, second segment becoming darker
brown on apical one-third, segments three and four dark brown;
thoracic pleura narrowly margined with testaceous to dull white;
femora dull testaceous marked with a series of large prominent,
black spots and armed with conspicuous black spines; thickly
clothed with decumbent, sericeous, flattened hairs, these inter-
spersed with semierect blackened hairs, the latter abundant and
conspicuous on upper surface of head.
Head strongly declivent, much more abruptly so than in nigerrimus.
Width across eyes .81 mm. (.78-.85), interocular space .43 mm.; rostrum
short, length .85 mm., attaining posterior margin of mesosternum, basal seg-
ment subequal to length of first antennal segment, length of this basal seg-
ment .21 mm.; length antennal segments, I .21 mm., II .92 mm., III .58 mm.
(.50-66), IV .31 mm. (28-.33). Length pronotum .71 mm., width pronotum
1.25 mm. (1.14-1.28)), length scutellum .61 mm. (57-.64). Lateral margins
of corium moderately and evenly rounded, membrane exceeding apex of
abdomen by distance caudad of apex of cuneus. Total length 3.51 mm.
(3.27-3.69) ; maximum width across hemelytra 1.50 mm. (1.35-1.56).
Holotype: Male, San Dizco County, Ca.irornia, 5-20-13 (E. P. Van
Duzee). In California Academy of Sciences collection. Allotype: San Dirco
County, Cairorntia, 6-8-13 (E. P. Van Duzee). Same deposition as holotype.
Paratypes: 3 males, same date as holotype and allotype. Deposited in the
California Academy of Sciences and private collections of the authors.
This new species is most closely related to nigerrimus (Van
Duzee) with which species it agrees in coloration and particularly
by the possession of the large black tibial spots and spines. It may
readily be separated from nigerrimus by the much shorter rostrum
that reaches only to the posterior margin of the mesosternum,
whereas in nigerrimus the rostrum reaches or slightly exceeds the
posterior coxae. In nigerrimus the basal segment of the rostrum
is considerably longer than the first antennal segment (.36 to .21)
whereas in brevitylus the two are subequal. In brevitylus the second
antennal segment is light brown rather than black, the interocular
space somewhat broader (brevitylus .43 mm., nigerrimus .306-.39
mm.), the black semierect hairs on the head more numerous and
extending further anteriorly on the frons. The shape of the anterior
portion of the head shows considerable difference in the two species
being more strongly declivent in brevitylus and as a consequence
less strongly produced forward.
AprIL, 1954] SNELLING—EXOMALOPIS 145
The authors wish to thank Dr. E. S. Ross of the California
Academy of Sciences for his kindness in locating hte specimens of
Psallus brevitylus in the Van Duzee collection.
REFERENCES
CarvaLyo, J. C. M.
1952. On the major classification of the Miridae (Hemiptera). (With
keys to subfamilies and tribes and a catalogue of the world
genera.) Anais. Da Academia Brasil. Cien. 24: 31-111.
Van Duzer, E. P.
1916. Synoptical keys to the genera of the North American Miridae.
U. California Pubs. Ent., 1: 199-216.
RECORDS OF EXOMALOPSIS SIDAE IN CALIFORNIA
AND BAJA CALIFORNIA
(Hymenoptera: Anthophoridae)
Roy R. SNELLING
Turlock, California
During the summer of 1953, the author had the opportunity
of collecting bees in Imperial County, California and the adjacent
Mexicali Valley, Baja California, Mexico. During the six weeks
of collecting spent in that area, the author collected quite a number
of a small species of Exomalopsis which was presumed to be E.
rifiventris Timberlake. However, when the author examined his
collection and papers it was found to be Exomalopsis sidae Cocke-
rell. In his recent revision of Exomalopsis,’ Timberlake states that
E. sidae is known only from the Mesilla Valley, New Mexico. How-
ever, there seems to be little doubt that this is the same species, as
the specimens collected by the author agree perfectly with New
Mexico specimens.
The revised distribution of Exomalopsis sidae Cockerell should
now include Arizona, California, and Baja California, Mexico.
New distributional data are as follows:
Arizona: 1 @, Tucson, June 16, 1951 (E. O. Johnson), on Sphaeralcea.
California: 1 ¢, 2 22, 1 mi. E. Calexico, Imperial Co., June 28, 1953
(R. R. Snelling), on Sida hederacea. Baja California, Mexico: a total of 13
females, 5 males from the following areas, from June 29 to July 17; 36k. S.
Mexicali, 7 k. NE. La Puerta, 12 k. SW. Mexicali, and Ejido Campeche,
females on Sida hederacea, two males on Gossypium, all collected by the
‘author.
1 Timberlake, P. H. 1947. Jour. New York Ent. Soc., 55: 85-106.
146 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
MONODONTOMERUS MONTIVAGUS ASHMEAD, A
PARASITE OF MEGACHILE CENTUNCULARIS (LINNAEUS)
(Hymenoptera )
A. E. MIcHELBACHER AND P. D. Hurp, Jr.
University of California, Berkeley
For many years the leaf cutting bee, Megachile centuncularis,
has used the guide mechanism of a casement window in the home of
the senior author in Berkeley, California, as a nesting site. Although
there six similar windows, only the one has been consistently
used. The groove of the metal guide is about 8 inches in length and
has a diameter just sufficient to accommodate the cells. Then entire
length of the groove is utilized in much the same manner as the
insect makes use of a hollow stem. Of course, if the window is
opened, the cells are crushed by the runner. However, if the window
is only partly opened, a good portion of the cells can be removed
without injury.
During the 1953 nesting season, the bees were especially am-
kitious, and after filling the groove with cells, the female in one
manner or another constructed another series of cells along side
of the metal groove. About March 15, 1954, the cells outside of the
groove were examined. An end cell was broken open and it was
found to be parasitized. The rest of the cells were held, and para-
sites emerged from five out of nine in the series.
The parasite was Monodontomerus montivagus Ashmead. This
is the first record of this parasite being reared from the genus
Megachile. Muesebeck, et al, (1951)+ listed the known hosts of this
parasite as follows: Choristoneura fumiferana (Clem.) ; Anthidium
emarginatum (Say); Dianthidium pudicum (Cress.); D. pudi-
cum consimile (Ashm.); Osmia cordata Robertson; Anthophora
abrupta Say; Anthophora linsleyi Timb.; A. occidentalis Cress.;
Melissodes sp.; and Xylocopa orpifex Smith.
As a matter of speculation, it is possible that cells constructed
in the metal groove are protected from the parasite, while those
which were built outside the groove were freely exposed to
parasitism.
1 Hymenoptera of America North of Mexico—Synoptic Catalog. United States
Department of Agriculture. Monograph No. 2:1-1420. 1951.
APRIL, 1954] LINDQUIST—-BLOWFLIES 147
FLIES ATTRACTED TO DECOMPOSING LIVER
IN LAKE COUNTY, CALIFORNIA
ArtTHuR W. LINDQUIST
U.S.D.A., Agr. Res. Adm., Bureau of Entomology and Plant Quarantine
Various species of flies visiting decomposing organic materials
are considered to be of economic importance. Phormia ragina
(Meig.), Phaenicia spp., and Callitroga macellaria (F.), which
breed in carrion, causes myiasis in soiled and moist wool of sheep.
In addition, P. regina is an invader of wounds in warm-blooded
animals and can be described as an obligatory necrobiot. These
flies, as well as other species, cause damage by ovipositing on meat
in abbatoirs, markets, and homes. Mechanical contamination of
foods and the distribution of noxious bacteria and viruses to
human food by these insects have long been considered to be of
public-health importance.
It is not generally recognized that, even though blow flies are
enemies of man and animals, they are also of great benefit to
mankind because they destroy dead animals and thus prevent
unsanitary conditions. Without blow fly larvae to reduce and
destroy the vast number of carcasses of wild and domestic animals
an unsightly and odoriferous condition would prevail. Blow fly
larvae can be prevented from developing in an animal carcass by
spraying it with DDT, lindane, or other insecticides, but the stench
from the carcasses is noxious and long-lasting.
From 1938 through 1941 a study was made of the seasonal and
relative abundance of the insects caught in a liver-baited trap in
Lake County, California. The trap was a cone-type, screen-wire
device (17 by 24 inches), almost identical with traps used by Par-
rish and Cushing (1938). It was set 4 feet above the ground in
partial shade about 30 feet from the shore of Clear Lake, near the
town of Nice. This locality has an elevation of 1300 feet and is
surrounded by mountains of the intercoastal range, some of which
rise to an altitude of 4100 feet. The Sacramento Valley, with an
elevation of 100 feet, lies approximately 50 air-line miles toward
the east.
On approximately the first and fifteenth day of each month
the flies were removed from the trap and weighed, the volume
determined, and the number of each species or genus ascertained
in a random 10-gram sample. A total of 78 collections containing
148 THE PAN-PACIFIC ENTOMOLOGIST [VOL, XxX, NO. 2
844 quarts of flies was made. The data obtained have been sum-
marized by months in Figure 1. Weather records from the official
Weather Bureau station at Upper Lake, located 5 miles from Nice,
were studied in relation to fly abundance.
Phormia regina. This was the most abundant species through-
out the spring, summer, and fall months. It accounted for about
40 to 88 per cent of the total flies taken during any month except _
in the winter. The greatest number caught during one month was
429,000 in May 1940. The total volume of all flies caught during
this month was 76 quarts. Breeding conditions were ideal during
the spring, with above-normal temperatures during most of May.
This species was caught every month except December 1939 and
December and February 1941, when cold, wet weather prevented
fly activity.
In Figure 1 it will be noted that the three most abundant species
—Phormia, Phaenicia spp., and Callitroga macellaria—are pro-
jected on a scale that is only one-fifteenth that of the other species.
This was necessary in order to accommodate the data on one figure.
Phaenicia spp.—These species were taken in most of the trap-
ping periods except during the winter. They accounted for approxi-
mately 3 to 18 per cent of the flies caught during the warmer
portion of the year.
Callitroga macellaria (the secondary screw-worm fly) and C.
hominivorax (Coq.) (the screw-worm fly). These were the most
interesting flies encountered in this study. C. hominivorax is the
primary species causing myiasis in warm-blooded animals. Neither
of these species is indigenous to the area, but C. macellaria was
caught every summer, whereas C. hominivorax was taken in only
one season during the four years. The latter is a comparatively
rare fly even in areas of high screw-worm incidence; the propor-
tion of this species to C. macellaria in trap catches may be one to
several hundred or thousand.
Neither species has a true hibernating stage. Declining tem-
peratures in the fall and winter either destroy all stages or lengthen
the developmental period so that mortalities are high (Parrish
1945, Lindquist 1945). As the weather becomes warmer in ‘the
spring, the species migrate from areas in which they survived the
winter. Mean temperatures of 49° to 54° F. for about three months
have been found to destroy these species (Parman 1945, Lindquist
1945, Parrish 1945).
#939
Jan Fe bMar AprMay JunJuly AugSept OctNov Dec
Ophyra. |
\ Seale:
10,000 Specimens
Sareo-
age
used
Ms ~~ iessostaelll —
Me aan
Syrthes-
1omy!e
Para-
luci lta sar ad soe
Seale:
77" 150,000 specimens
Fhormia
Pi hacnic a
Gillitr Taga if
Macellara
1940
Jan febMar Apr May Jun July Ayg Sep
lov Dec
194!
Jan FebMarAprMay Jun Jilly Ayg Sept Oct Nov Dee
Fig. 1—Seasonal abundance of flies caught in a liver-baited trap at Nice, California.
[PS6L “ludy
-LSINOGNIT
SHTTAMOTE
é6rl
150 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
It appears likely that the winter of 1939-1940 was sufficiently
mild so that C. macellaria at least survived as far north as Visalia,
California. The mean temperatures for December, January, and
February at this location were 5.7°, 4.8°, and 3.1°, respectively,
above normal. The average mean was 52.3°, which may have per-
mitted both species to survive. It appears likely that the early
(June) appearance of C. macellaria in the trap at Nice is accounted
for by the overwintering of the species farther north than is usual
in California. The species was first observed in the trap collections
of July 17-30, 1939, June 14-30, 1940, and August 1-15, 1941. No
specimens were ever found after December 15. During August,
September, and October 1940 an enormous population had built
up. In september 46 per cent of the entire catch was of this species.
Stewart and Roessler (1942), reporting on work at Davis,
California, found that this species appeared in liver-baited traps
in late July 1936. It was the predominating fly during August,
September, and October. Bruce and Knipling (1936) at Ames,
Iowa, caught C. macellaria in liver-baited traps in June 1933 and
1934. The species had apparently migrated from overwintering
areas in Texas.
C. hominivorax was observed in the catch of flies taken during
September 17-27, 1940. It is possible that the species was present
in earlier trap collections, but because it is a relatively scarce
insect and bears a close resemblance to C. macellaria it may have
been overlooked. In the October 1-15 catch four specimens of
C. macellaria were found in 31% quarts of the 32-quart catch, and
one fly was found in the 10-gram sample examined from the
October 15-30 catch of flies. No flies were found during November.
A number of screw-worm cases were reported in the county during
September and October. Larvae collected from the wounds of
these domestic animals were identified as C. hominivorax.
Ophyra spp. These flies were captured every trapping period
over 7 to 8 months of each year. They constituted approximately
2 to 5 per cent of the total flies caught each month. As shown in
Vigure 1, this species was fourth in abundance. It is the last in a
succession of flies to oviposit in carrion. The larvae perform the
final clean-up of a carcass and appear to thrive on fat, ligamentous
tissue, and slime that remain after other fly larvae have left.
Sarcophaga spp. These flies were present in the trap catches
APRIL, 1954] LINDQUIST—-BLOWFLIES 151
during the greater part of the year. The number taken in a month
ranged from less than 1000 up to 8000.
Musca domestica L. This species was captured each month
from April through November. The number caught ranged up to
11,000 in a month and constituted up to 8.7 per cent of the total
flies taken. Because this fly walks over foods in homes and res-
taurants after visiting all sorts of decomposing matter, including
carrion, it is one of the most dangerous enemies of man.
Calliphora spp. These species are important because they fre-
quently visit homes and contaminate meat by laying eggs on it.
These flies predominated during the winter and accounted for 11
to 74 per cent of all flies taken during this period. Figure 1 shows
that they are prevalent during the spring and fall but disappear
almost entirely in the summer.
Synthesiomyia nudiseta. Late summer and fall was the opti-
mum period of activity of this insect. It occasionally visits houses
but is of little economic importance. :
Paralucilia wheeleri (Hough). This fly closely resembles C.
macellaria and C. hominivorax. It appears to vary in numbers
from year to year more than do some of the other species. Speci-
mens were frequently observed in the catch but not in the 10-gram
sample, which was too small to quantitatively measure low num-
bers. For some unknown reason the incidence of the species was
low during 1939 and higher during 1941. Deonier and Knipling
(1940) reported on the distribution and life history of this species
in Arizona.
Miscellaneous flies—A considerable number of small Diptera
were taken in nearly every trap. They accounted for 2 to 15 per
cent of the various catches of flies. No attempt was made to segre-
gate the different species.
LITERATURE CITED
Bruce, W. G. ano E. F. Knretine
1936. Seasonal appearance and relative abundance of flies attracted
to baited traps. Iowa State Coll. Jour. Sci. 1(4): 361-366.
Deonter, C. C., ann E. F. Knrpiine
1940. The biology of Compsomyiops wheeleri (Hough) and description
of the larva. Ann. Ent. Soc. Amer. 33(3) : 578-582.
Linpouist, ArtHUR W., anp W. L. Barrett
1945. Overwintering of Cochliomyia americana at Uvalde, Texas. Jour.
Econ. Ent. 38(1): 77-83.
152 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
Parman, D. C.
1945. Effect of weather on Cochliomyia americana and a review of
methods of economic applications of the study. Jour. Econ. Ent.
38(1): 66-76.
ParrisH, H. E.
1945. Overwintering of Cochliomyia americana and C. macellaria at
Menard, Texas. Jour. Econ. Ent. 38(1) : 83-84.
ParrisH, H. E., anp Emory C. CusHine
1938. Locations for blowfly traps: abundance and activity of blowflies
and other flies in Menard County. Texas. Jour. Econ. Ent. 31(6):
750-763.
Stewart, M. A., anp E. B. RoressLer
1942. The seasonal distribution of myiasis-producing Diptera. Jour.
Econ. Ent.. 35(3) : 408-411.
A CASE OF REVERSE PREDATION IN THE CARABIDAE
Wiiiiam V, GARNER
University of California, Berkeley
On July 31, 1952 Dr. J. W. MacSwain collected three living
larvae of Calosoma semilaeve LeConte for the author in a Ladino
clover field at Artois, Glenn County, California. Each of the speci-
mens was placed in a small pill-box with a living prepupal noctuid
larva as food, until arrival in Berkeley the following day.
Upon examination in the laboratory it was found that two of
the three carabids had been entirely consumed by their supposed
prey. Immediate dissection of the cutworms showed their intestinal
tract to be clean, indicating a very rapid digestion. Examination
of fecal pellets from the pill-boxes, however, revealed many small
pieces of chitin and identifiable portions, such as legs, head capsule,
tergites and urogomphi.
Whether the Calosoma larvae were attacked and killed, or
whether they first died and were then consumed can only be con-
jectured. It is well known, however, that cutworms are often highly
cannibalistic, as are most Carabid larvae, particularly when con-
fined to a limited amount of space.
The literature is replete with examples of certain of the
Carabidae feeding on cutworms and other lepidopterous larvae,
but this is the first case to the author’s knowledge where the reverse
is apparently true.
APRIL, 1954] HUSSEY—PSELLIOPUS . 153
TWO NEW SPECIES OF PSELLIOPUS AND SOME
DISTRIBUTIONAL NOTES
(Hemiptera, Reduviidae )
Ro anp F. Hussey
Biology Department, University of Florida, Gainesville
This paper is one of several now in preparation that are based
upon material in the Museum of Zoology of the University of
Michigan, where the types of the new species are deposited. I wish
here to express my deep appreciation to Dr. J. Speed Rogers,
Director, and to Dr. T. H. Hubbell, Curator of Insects, for the
privilege of working over the extensive collections of Hemiptera
under their care. Among the thirteen species of Pselliopus in the col-
lection, four appear to be undescribed. Two of these, from Arizona
and from New Mexico, are represented by females only; the other
two are described herewith. As in other recent papers, I have
expressed all comparative measurements here in hundredths of a
millimeter.
Pselliopus karlenae Hussey, new species
Length: 12.2-13.1 mm., width of pronotum 2.9-3.2 mm.
Head black above, with a yellow mark above and in front of each eye
and another at the side behind the eye, also a small yellow spot between the
ocelli and a triangular one between the bases of the antennae; genae and
gula yellow. First two antennal segments black, the others testaceous, first
segment with three pale annuli of which the third is at the apex, second
segment with a single pale ring at the middle; third segment with an obso-
lete sub-basal fuscous ring. Rostrum yellow, the first segment with a large
piceous spot on each side at the middle, the second with a piceous annulus
at the base, the third with a narrow piceous line on the lower side. Anterior
lobe of the pronotum black, the collar (including the anterior angles), an
irregular vitta on each side of the middle line, and a rather large spot on
each side yellow; posterior lobe yellow, finely and closely concolorously
punctate, the lateral angles with a triangular black spot enclosing the black
spines, this spot narrowed behind and sometimes joining the blackish spot at
the middle of the explanate postero-lateral margins. Scutellum black on the
basal half, with a tomentose white dot each side near the base, the broadly
foliaceous apex yellow. Body above with fine, fairly thick, erect golden
pubescence. Hemelytra translucent or transparent, brown, the cubital veins
prominent, fuscous; corium and veins of the clavus rather thickly provided
with short, curved golden hairs. Dorsum of the abdomen black; connexival
segments above and below sanguineous, broadly banded with black on the
anterior portion, the extreme anterior margin sometimes narrowly yellow.
Under side yellow, the pleura largely black, each ventral segment with a
narrow black band on the posterior margin and also on the front margin
toward the sides. Pleura, coxae, and basal segments of the venter at the
154 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 2
sides with spots of white tomentum, the mesosternum densely white tomen-
tose, the metasternum less so except at the sides. Femora and tibiae yellow,
the femora with five black annuli (some of them more or less interrupted),
the tibiae with three black annuli on the basal half and with an abbreviated
brownish stripe on the apical half of the dorsal face. Male genital segment
with two black stripes below on the posterior half, these uniting at the base
of the median spine; parameres and median spine of hypopygium black.
Head shorter than the pronotum (218:272), four-fifths longer than its
own width across the eyes (218:120), gradually narrowed behind the eyes.
Ratios of lengths of antennal segments I-IV, 441:185:277:155. Pronotum
smooth or nearly so, the punctures of the posterior lobe extremely shallow;
median impression of the anterior lobe fairly deep, continued as a broad
shallow depression onto the posterior lobe but not attaining the base of the
latter. Humeral spines short, conical, directed outward, equalling or slightly
surpassing the lateral angles. Postero-lateral margins rather narrowly expla-
nate, strongly reflexed behind and lightly sinuate, produced as very short
and rather wide lobular processes at the posterior angles. Hind margin of
the pronotum most lightly convex before the scutellum. Disk of the scutellum
with a Y-shaped ridge whose median (apical) arm is abbreviated behind,
evanescent at about the middle of the scutellum; apical portion moderately
broad, horizontal, its postero-lateral margins narrowly reflexed, vertical;
apical portion less pilose than the basal part; total length of the scutellum
one-third greater than that of the anterior lobe of the pronotum (147:110).
Margin of the male hypopygium with a long, rather robust median
spine which is bifurcate for only a short distance at the tip, the apices dis-
tinctly divergent (Fig. 1). Parameres as seen from behind fusiform, rather
strongly curved on the inner side, setulose near the pointed tips and scantily
so on the inner side; when seen from the side the tips of the parameres are
rather abruptly curved upward. Last tergite of the male abdomen strongly
arched transversely to accommodate the hypopygial spine.
Holotype male and allotype female: Honpuras, Dept. Mor-
AZAN, Mt. CACULATEPE, ELEVATION 3700—4200 FEET, Aug. 6, 1948
(T. H. Hubbell). Paratypes (all collected by Dr. Hubbell): 1 ¢,
3 9, same data as the preceding; 1 9, Cerro Uyucaguatal, 4500-—
5000 ft., July 12, 1948; 1 9, five kilometers southwest of Suyapa,
5300 ft., Aug. 5, 1948; also two paratypes, ¢' and 9, from Mt.
Caculatepe in my collection. These localities are all in the vicinity
of the Escuela Agricola Panamericana at Zamorano, about 35 kilo-
meters southeast of Tegucigalpa. The specimens from Mt. Cacula-
tepe were taken by sweeping and by beating shrubbery, and numer-
ous examples of P. zebra (Stal) were collected with them.
This species is closely allied to P. zebra but is readily separable
by the first antennal segment which bears three pale annuli instead
of four, by the sanguineous areas on the connexival segments, by
the male genitalia, and by the strongly arched last tergite of the
AprIL, 1954] HUSSEY—PSELLIOPUS 155
male abdomen. The specimens of zebra before me agree with Stal’s
description in having the first antennal segment quadriannulate,
and Champion, in the Biologia (Vol. 2, p. 247) implied that this
is the usual condition, yet all three of his figures of zebra and
Se)
EXPLANATION OF FIGURES
Fig. 1 Pselliopus karlenae Hussey, Fig. 2 Pselliopus zebra (Stal),
Fig. 3 Pselliopus latispina Hussey. At left, apex of male hypopygium, with
median spine and parameres, and outline of last tergite of male abdomen,
as seen from behind. At right, left paramere as seen from the side.
156 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 2
varieties (op. cit., Pl. 15) show this segment as triannulate? In P.
zebra (Fig. 2) the median spine of the hypogydial margin is cleft
or sulcate on the apical third and the tips lie parallel and con-
tiguous; the parameres are lightly clavate, blunt at the tips, and
thickly pilose on all sides for some distance before the apex.
P. karlenae may well have been confused with P. zebra in the
past, particularly if only females were at hand, but I cannot
identify it with any of the “varieties” described by Champion. The
coloration of the anterior pronotal lobe (but not the posterior one)
is quite similar to that shown by Champion in Fig. 5 of Plate 15,
but in the present species the black color extends onto the sides
to enclose a large yellow lateral spot.
Pselliopus latispina Hussey, new species
Length, ¢ 10.9 mm., 2 12.8-13.1 mm.; width of pronotum, % 3.1 mm.,
Q 3.7-3.9 mm.
Yellowish ochraceous (as in P. barberi Davis), the legs more yellowish,
marked above with black as follows: the tylus entirely, two lines forming a
V leading from the middle line between the eyes straight to the antennae, the
dorsal portion of the head from the base of the swollen part to the middle
of the eyes (except a round yellow spot between the ocelli), joined behind
the ocelli with a broad vertical band on the side of the head, where a narrow
black line extends forward from the lower edge of this band to the postero-
ventral angle of the eye, an anterolateral spot on each side of the anterior
pronotal lobe, a narrow transverse uneven line (sometimes obsolete) in the
interlobular sulcus, the blunt humeral spines and a very narrow area around
their bases, an oblique elongated marginal spot at the middle of the strongly
reflexed postero-lateral margins of the pronotum, the basal part of the scutel-
lum (which bears a subbasal spot of white tomentum at each side), and a
black band (both above and below) at the basal third of each connexival
segment, these bands abbreviated inwardly and widened outwardly to reach
the anterior angles of their respective segments. Antennae colored as in
P. karlenae; first two rostral segments marked as in that species, the third
almost wholly black. Legs yellow, the femora with five narrow black bands
of which the apical one is somewhat the widest; front and middle tibiae
with four black bands; hind tibiae with three such bands on the basal half
and with a blackish stripe on the anterior and the posterior faces of the
apical half; tarsi dark brown. Ochraceous color of the abdominal tergites
plainly visible through the translucent hemelytra, the clavus somewhat more
embrowned than the corium or the membrane. Dorsum with rather short
and sparse erect pilosity, the curved hairs on the hemelytra more sparse
than in P. karlenae. Venter ochraceous, each segment narrowly banded with
black on the anterior margin, and with a second, abbreviated, black band
on about the outer fourth of its width, none of these bands reaching the
inner margin of the connexivum; the abbreviated markings on the con-
nexivum below dislocated with respect to the fasciae of the ventral segments.
AprIL, 1954] HUSSEY—PSELLIOPUS 157
Male genital segment with a pair of blackish spots on the ventral side before
the apex.
Head one-fourth shorter than the median length of the pronotum
(é 188:250), three-fifths longer than its own width across the eyes (188:
117), the interocular width more than twice the width of an eye (61:28).
First antennal segment two and one-third times as long as the second, more
than one-half longer than the third (350:150:220), and nearly twice as long
as the head (350:188). First rostral segment attaining the middle of the
eyes, slightly shorter than the second (93:100) when both are measured on
the upper edge.
Pronotum smooth or nearly so, the posterior lobe flattened_but not or
hardly depressed along the middle line, very finely but not thickly punctate,
the punctures scarcely impressed, less thickly pilose than the anterior lobe.
Anterior angles nodose-tuberculate; humeral spines blunt, directed slightly
backward, not or scarcely surpassing the lateral angles; postero-lateral
margins rather widely explanate, strongly reflexed and lightly sinuate, pro-
duced at the posterior angles into finely punctulate lobules as long as the
transverse width of an eye, inner margin of the lobules forming a right angle
with the transverse posterior margin of the pronotum.
Scutellum with a Y-shaped ridge on the basal part, the median (apical)
arm of this Y evanescent at the middle of the scutellum but forming a con-
spicuous pale calloused spot; produced apical portion rather broad, finely
punctate, obliquely reflexed as seen from the side, with a deep cup-like
impression before the apex, the postero-lateral margins moderately reflexed.
Margin of the male hypopygium with a long, broadly triangular median
spine which appears not to be sulcate or furcate; parameres very slender
(Fig. 3). In the only male before me the spine is directed obliquely forward
and upward under the last tergite of the abdomen.
Holotype male, Mexico, STATE oF HIDALGO, 6.5. KM. NORTH OF
DurANco on Camino NACIONAL NO. 1, ELEVATION 6500 FEET, Aug-
ust 29, 1948 (T. H. Hubbell). Allotype, 2 and one paratype 9:
MEXICO, State of Nuevo Leon, 15 miles north of Linares, Dec. 16,
1941 (1. J. Cantrall and J. J. Friauf), the paratype in my collection.
Easily distinguished from the other species of Pselliopus before
me by the much larger and more strongly produced posterior lobe-
like processes of the postero-lateral margins of the pronotum. Other
distinguishing characters are the almost complete absence of a
median impression on the posterior lobe of the pronotum, and the
interrupted and dislocated transverse black fasciae of the venter and
connexivum below. In size and color, and also in the male genital
characters, it is perhaps nearest to P. barberi Davis, but apart from
the differences already indicated, this latter species has the para-
meres somewhat longer and more strongly twice-curved, the scutel-
lum is not obliquely reflexed on the apical part and lacks the cup-
158 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
like pre-apical impression, the transverse base of the pronotum is
relatively wider, and the venter is without black bands.
PSELLIOPUS LATIFASCIATUS Barber
Three specimens in the Michigan collection from Alachua
County, Florida, constitute the first records of the species from that
state. PSELLIOPUS CINCTUS (Fabricius)
In his “Heteroptera of Eastern North America” Blatchley
(1926, p. 574) referred to this species as more southerly in its
distribution than P. barberi, and stated that it had been taken only
in the southern third of Indiana. The Museum of the University of
Michigan has specimens from Lake County, Indiana, and from
Cook County, Ilinois, both of which border on Lake Michigan and
lie in the northernmost part of their respective states. There is also
one individual from southwestern Michigan, collected by G. Orton
Sept. 7, 1949, in Allegan County (which also borders on Lake
Michigan), approximately seven miles east of Saugatuck. This
species has not been known before from Michigan.
ATRACHELUS CINEREUS (Fabricius)
In 1921 (Psyche, 28: 10) I reported the capture of two ex-
amples of this species by the late A. W. Andrews in Wayne County,
Michigan, during the summer of 1918. These still are the only
specimens I have seen from Michigan or from adjacent areas.
RHINIGIA CINCTIVENTRIS (Stal)
The Michigan collection has one example from Clarke County,
Alabama, taken by A. F. Archer in May, 1935, at Salt Mountain,
six miles south of Jackson and approximately 50 miles north of
Mobile. I believe this is the first record for this species east of the
Mississippi River.
LEPTIDIELLA BREVIPENNIS (MULSANT)
REARED FROM TOYON
(Coleoptera: Cerambycidae)
The minute introduced longhorn Leptidiella brevipennis (Mul-
sant) has been recorded from California by Linhley (1934, Pan-
Pacific Ent., 9 (4):170), and Middlekauff and Underhill (1949.
Pan-Pacific Ent., 25(3) :128). Mr. L. W. Swan obtained a new
host and distributional record by rearing in 1950 a specimen (det.
E. G. Linsley) from a native shrub, toyon or Christmas berry,
Photinia arbutifolia, at Stanford University, Santa Clara Co., Cali-
fornia——Hucu Bb. Leecu, California Academy of Sciences, San
Francisco.
APRIL, 1954] LEE—PHOTOTROPISM 159
THE ABSENCE OF NEGATIVE PHOTOTROPISM IN THE
MEXICAN CHICKEN BUG, HAEMATOSIPHON INODORUS
(DUGES)
(Hemiptera: Cimicidae)
Ropert D. Lee
Department of Entomology, School of Tropical and Preventive Medicine,
Loma Linda, California
The nocturnal feeding habits of the common bedbug, Cimex
lectularius Linn., and other species of the family Cimicidae are
well known. In experiments with this species, the bugs were gen-
erally fed in darkness (Johnson, 1942) or in partial darkness. C.
lectularius will move toward the dark when subjected to a bright
light (Kassianoff, 1937). In contrast to this R. E. Ryckman (per-
sonal communication) has observed the feeding of Haematosiphon
inodorus (Duges) on nestling barn owls in the presence of abun-
dant light under field conditions. The owl nests were in cave-like
holes ten to twelve feet down from the top of a 35 foot bank on
the south side of the Santa Ana River near Norco, California. H.
inodorus will feed on chickens in the laboratory in bright light.
Because of these and other observations of the actions of this bug,
it was decided to attempt to determine whether it does or does not
exhibit a photonegative tropism.
One hundred H. inodorus adults were taken at random from the
main colony and placed in a jar with a screw-type lid; the jar ‘was
7 inches long and 184 inches in diameter. One half of the length
of the jar was painted black on the outside; the other end
of the jar was left unpainted. The jar was placed on a light back-
ground under an inverted aquarium. Two 200-watt lights were
placed approximately 12 inches from the middle of the jar just
outside the aquarium. The aquarium served to reduce the radiation
of heat between the light source and the jar containing the bugs,
thereby tending to decrease any tropism to heat which the insects
might show. A nearly light-proof room was used in which to
conduct the experiment.
The bugs were concentrated in the painted area by tapping
that end of the jar while it was held lower than the unpainted
area. The jar was then quickly placed under the aquarium. For
five minutes the lights were switched on simultaneously. Twelve
bugs had moved into the unpainted area during the dark period.
After five minutes of light, another dozen bugs joined this group.
Occasionally one or two bugs would run into the darkened portion
of the jar but would either run out again or be replaced by one or
160 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 2
two other bugs. After the lights had been on for ten minutes, the
. number in the unpainted area was approximately the same. No
fear of the light seemed to be indicated. Copulation by several pairs
took place. There was an unsuccessful attempt by some to climb
the walls of the jar.
The experiment was repeated with the procedure reversed; the
bugs were concentrated in the light end of the jar before the five
minute period of darkness. When the lights went on, apparently
only a very few had shifted to the painted end of the jar during
the dark period. After five minutes of light, the bugs seemed to be
grouped toward the end of the unpainted area away from the
dark. A number again were seen copulating in the light. At the
end of ten minutes of light, only a very few had moved into the
painted, dark portion of the jar.
A similar experiment was set up canine one hundred Cimex
lectularius adults. The bugs were concentrated in the dark end of
the jar, and the experiment was conducted as before. At the end
of the five minute dark period, five insects were seen in the clear
area. At the end of the first five minute light period, there were
still only five Cimex in the unpainted end of the jar. After ten
minutes of light, this number had dropped to two. During the
time the light was on, a few individuals were seen to come from
the dark zone, go into the unpainted area, and then go back to the
dark zone.
The Cimex were then concentrated in the unpainted area and
quickly put under the aquarium. The lights were turned off for five
minutes as before. When the lights were turned on after five min-
utes of darkness, the large majority of Cimex were still in the clear
area. After five minutes of light, only nine bugs were still in the
unpainted zone.
From these experiments, from the observations of Ryckman
in the field, and from observations of the general lack of negative
reaction of the insect to the light in the laboratory, H. inodorus
appears to exhibit an absence of the negative phototropism seen in
Cimex lectularius. In fact, H. inodorus may be said to show a
slight positive phototropism.
Jounson, C. G. LITERATURE CITED
1942. The ecology of the bed-bug, Cimex lectularius L., in Britain.
Jour. Hyg. 41(4): 345-461.
Kasst1AnorF, L.
1937. Etude morphologique et biologique de la famille des Cimicidés.
Ann. Parasit. hum. comp. 15(5) : 385-408.
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Vol. XXX JULY, 1954 No. 3
THE
PAN-PACIFIC ENTOMOLOGIST
CONTENTS
JENSEN—Notes of the potato psyllid, Paratrioza cockerelli (Sulc).........-. 161
CAMRAS—A new species of Zodion from California....._...-....-.------------- 165
JEWETT—New stoneflies from California and Oregon.....................-:0-000-- 167
BOUDREAUX—New species of Tetranychid mites... .......eeccceceeeeeees 181
SEIDEL—Two new dipteran parasites of Autographa californica................ 186
DENNING—New species of Lepidostoma.....u......-......s-c-cseeseesscecenencceenenneceees 187
ROSENSTIEL—Another weevil injurious to strawberries.............-.---------- 194
MOORE—Notes on Endeodes LeConte with a description of a new species
PE OU agar Cr nO TNT a ee fe ee ee teat aoe ee De 2 A ope eae 195
HURD—A polyiypic interpretation of the California carpenter bee
Xylocopa californica with the description of a new subspecies and
notes on a possible polytopic form... e.-seceeeeeceecceecesneeeneeseccnceenceeneee 199
ROZEN—Morphological description of the larva of Oreopasites van-
duzeer Gockeretla uy -tee. vere ee) eee die Ee a Lene esl oh eee et 203
MOORE—An efficient method of collecting dung beetles... .eee-eneeeenes 208
BAILEY—A review of the genus Rhipidothrips Uzel. uu... e-seeneneeeenee 209
PITELKA—Use of bird nest by bumblebee... eeeeeeeeneceeneneeeennee 220
CAUSEY—New records and species of millipedes from the western United
StatesrandsGalrad am Area. -ces 8 ee Pere ie Oe, ORO Reena Re Se 221
BELKIN—The dorsal hairless setal ring of mosquito pupae.............--.0------ 227
ZOOLOGICAL NOMENCLATURE icc chk pace lescesecoctchlebeonteccecedeuatsen 179
EO) CURING TG Bie oes Perea Seas oti top Rt ol tens ed kg ere ee De weed ce olin. 208
SAN FRANCISCO, CALIFORNIA + 1954
Published by the PACIFIC COAST ENTOMOLOGICAL SOCIETY
in cooperation with THE CALIFORNIA ACADEMY OF SCIENCES
THE PAN-PACIFIC ENTOMOLOGIST
EDITORIAL BOARD
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by A. Earl Pritchard and Edward W. Baker
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systematics, identification, and economics of the “Red Spiders”.
Synoptic keys have been prepared, descriptions are presented for
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ty species are described as new.
Publication date—December, 1954.
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Entered as second class matter, February 10, 1925, at the post office at
San Francisco, under act of August 24, 1912.
The Pan-Pacific Entomologist
Vol. XXX July, 1954 No. 3
NOTES ON THE POTATO PSYLLID, PARATRIOZA
COCKERELLI (SULC)
(Hemiptera: Psyllidae)
D. D. JENSEN
University of California, Berkeley
The potato psyllid, Paratrioza cockerelli (Sulc), sporadically
has been a major pest of potatoes and less frequently of tomatoes
in Utah, Colorado, Wyoming, Montana, Nebraska, and North
Dakota. It causes ‘a destructive disease of these plants known as
psyllid yellows, which is due to the feeding of the nymphs. The
disease symptoms closely resemble those caused by virus, but
psyllid yellows apparently results from a toxin rather than a virus
introduced by the nymphs.
Considerable work has been done on the relation of the insect
to the disease and on the host plants and life history of the psyllid
in the areas of greatest damage. However, the site of overwintering
and the source of the adult psyllids which infest the early potatoes
and other host plants in May and June in the Rocky Mountain
states have remained uncertain. The best available evidence in-
dicates that the potato psyllid only rarely survives the winter out
of doors in the regions subject to the greatest summer damage.
(Wallis, 1946; Pletsch, 1947.).
Romney (1939) reported that P. cockerelli breeds abundantly
on Lycium andersonit A. Gray from January to May in the semi-
desert areas of southern Arizona, New Mexico, and Texas below
3,000 feet. He states that the adults disappear from these plants
by the middle of June. In late October or November an influx of
adults returns to Lycium from an unknown source. He suggests
that the psyllids produced during the winter in the southern breed-
ing area migrate north and provide the population which infests
the fields of Colorado in May and June. He derived additional
evidence for this idea from the fact that the beet leafhopper,
Circulifer tenellus (Baker), is known to make such a movement
north and both species were taken in insect traps used in studying
the beet leafhopper.
The psyllids are believed to leave the winter breeding plants
in the spring because these plants dry up. Moreover the high
summer temperatures in many of the southern areas are lethal to
162 THE PAN-PACIFICG ENTOMOLOGIST [ VOL. Xxx, NO. 3
the psyllid, particularly in the egg and nymphal stages.
Current records are adding strong circumstancial evidence for
Romney’s suggestion that potato psyllids migrate in May and June
to the Rocky Mountain States from winter breeding areas in the
Southwest. 3
Wallis (1954) reported that in March 1954 the psyllid popula-
tions on Lyciwm in southwestern Texas, southern New Mexico,
Arizona, southern California, and southern Nevada were much
higher than at any time in the past 10 years. The number of adults
per 100 sweeps ranged from 28 in southern Nevada to 128 in
Arizona. He cautioned that if weather conditions were right for
a northward movement of the psyllids in May and June this could
be an epidemic year in some of the northern potato and tomato
growing areas.
The Cooperative Economic Insect Report (U.S.D.A.) for May
28. 1954 (Vol. 4, No. 21) carries an indication that a large influx
of psyllids did occur into eastern Colorado during the middle of
May. |
“Colorado. Averaging 87 adults per 100 sweeps and many eggs
laid. During the 6 days preceding May 20, large movement of
adults into eastern counties. Strong indications that an epidemic
season may be developing (Daniels). Utah. Increased abundance
in some localities on matrimonyvine. On basis of 100 sweeps follow-
ing collected this week: Bountiful 8; Grainger 12, Bennion 8,
Spanish Fork 4 to 12, Fayette 12, Centerfield 28, Gunnison 92,
(Knowlton). Arizona. [Psyllids] Left potato areas of Pinal and
Maricopa counties. (Ariz. Coop. Rept.)”
Whether the disappearance of psyllids from Pinal and Maricopa
Counties in Arizona was due to migration or death of the psyllids
was not reported. U.S. Weather Bureau records show that tempera-
tures in this area reached as high as 114° F. with an average daily
maximum of 93° during May, 1954. According to List (1939) the
optimum temperature for P. cockerelli is 80 degrees and tempera-
tures over 90 degrees are severely deleterious. He noted also that
“high temperatues make the adults very restless and may cause
them to take flight and thus reach air currents that carry them
great distances.”
Certain recent collections of Paratrioza cockerelli adults in Cali-
fornia and Nevada are of interest in connection with the over-
wintering of the species and because of the preference indicated
JULY, 1954] JENSEN—POTATO PSYLLID 163
by the adults for certain plants outside of the Solanaceae—the
family to which all known breeding host plants belong.
On April 2, 1951, P. D. Hurd and J. W. MacSwain (University
of California, Berkeley) found adult potato psyllids on Ephedra sp.
(Gnetaceae) in great abundance at Cima, San Bernardino County,
California. The presence of the psyllids on this plant appeared to
be more than mere random chance because comparatively few
psyllids were found on other plant species in this relatively barren
area.
Two years later, on April 1, 1953, Dr. MacSwain found adult
psyllids in incredibly large numbers at an elevation of 5,000 feet
in the Charleston Mountains, Clark County, Nevada, approximately
20 miles northwest of Las Vegas. In this area the night tempera-
ture reached freezing during this period.
The very dark-colored adults were present on certain plants,
such as Arctostaphylos pungens and Garrya flavescens, in such
numbers that two sweeps of the net against the side of a bush
yielded over one thousand adults when shaken down into the
bottom of the net and emptied into a bottle.
The population on Pinus monophylla was heavy but not as
dense as on Arctostaphylos or Garrya. The population on Juniperus
Utahensis was light to moderate and that on Larreya tridentata
was light. Certain plants, such as Cercocarpus, were comapratively
free of psyllids.
The breeding hosts and origin of these psyllids are unknown.
Those collected at Cima, in 1951, were apparently migrating be-
cause there were no solanaceous plants in the vicinity on which
they could have bred. Although Clokey (1951) lists Nicotiana,
Datura, Physalis, Solanum and Lycium andersonii as solanaceous
plants occuring in the Charleston Mountains, it seems improbable
that this large population of psyllids had been produced locally as
a spring generation. The breeding hosts (primarily Lycium ander-
sonit) occur at approximately 4,000 feet elevation, and it is un-
likely that the winter climate in this area would have been mild
enough to produce the high populations found at 5,000 feet April
1, on plants which were not breeding hosts of the psyllid.
It seems more probable that the psyllids collected at Cima and
in the Charleston Mountains were produced elsewhere in southern
California and southern Nevada and had been carried north by
wind currents,
104, THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXX, NO. 3
Romney’s observations of potato psyllid disappearance from
southern Arizona, New Mexico, and Texas in the spring, and an
influx in the fall seems to have its parallel in southern California
as well. Dr. R. C. Dickson, University of California, Riverside, in-
formed the writer that he checked certain solanaceous plants in
the Imperial Valley every two weeks during the late summer and
fall of 1952 for insects and virus diseases. He found that Lycium
plants at Niland, which had been free of psyllids two weeks earlier,
were heavily infested with adult psyllids early in November.
According to U. S. Weather Bureau records, air movements
associated with storm centers and about high pressure areas could
theoretically explain the movement of psyllids in wind currents
between the southern California-Arizona area and the Inter-
Mountain region. |
In the fall months, high pressure areas commonly occur in the
Great Basin, typically in: Nevada. These result in a flow of air
across southern Idaho, Utah, Arizona, and out to sea across south-
ern California. This air movement frequently develops into winds,
sometimes called Santa Ana winds, which result from the air be-
coming funneled down some of the canyons south of the Tehachapi
Mountains. Such air movement could transport adult psyllids
from the Inter-Mountain States to the southwestern areas.
In the spring, the high presstire areas more commonly occur
in the midwest and the flow of air is in the opposite direction, mov-
ing from southern California into the Inter-mountan States.
Populations of psyllids overwintering or being produced in the
southwest during the winter and spring months could be trans-
ported into the Inter-mountain regions during May and June.
The feasibility of the idea that psyllids might be carried long
distances in the air is supported by the fact that Glick (1939),
collecting insects by airplane in Durango, Mexico, took P. cock-
erelli more frequently than any other insect species at all altitudes
' from 100 feet to 4,000 feet.
Other recent collections of the potato psyllid from non-
cultivated areas include the following: adults abundant on Phacelia
sp., 7 miles east of Walker Pass, Kern County, California, April
25, 1952 (P. D. Hurd, Jr.) ; adults on Lepidospartum squamatum,
30 miles east of Sells, Pima County, Arizona, October 29, 1952
(E. G. Linsley and R. F. Smith) ; a few adults taken on Artemisia
tridentata, Pinus flexulis, and P. aristata, White Mountain Station
JuLy, 1954] CAMRAS—ZODION 165
(10,200 feet elevation), Mono County, California, April 25, June
23, 1953 (J. W. MacSwain).
It is hoped that by calling attention to this interesting problem,
more entomologists in the western states will make observations and
collections which may aid in clarifying this aspect of the potato
psyllid’s ecology.
REFERENCES
CLOKEY, Ira W.
1951. Flora of the Charleston Mountains, Clark County, Nevada. Univ.
Calif. Pub. in Botany 24:1-274.
Guick, P. A:
1939. The Distribution of Insects, Spiders, and Mites in the Air, U.S.
D.A. Tech. Bull. 673, 151 pp.
List, G. M.
1939. The Effect of Temperature upon Egg Deposition, Ege Hatch and
Nymphal Development of Paratrioza cockerelli (Sule). Jour. Econ.
Ent. 32:30-36.
Puierscu, D. J.
1947. The Potato Psyllid, Paratrioza cockerelli (Sulc), Its Biology and
Control. Montana Agric. Expt. Sta. Tech. Bull. 446.
Romney, V. E.
1939. Breeding Areas of the Tomato Psyllid, Paratrioza cockerell: (Sulc).
Jour. Econ. Ent. 32(1) :150..
Watuiis, R. L.
1946. Seasonal Occurence of the Potato Psyllid in the North Platte
Valley. Jour.. Econ. Ent. 39(6) :689-694.
1954. Potato Psyllid Numerous in Southern Breeding Areas. U.S.D.A.
Coop. Econ. Insect Report 4(13) :256.
A NEW SPECIES OF ZODION FROM CALIFORNIA
(Diptera: Conopidae)
SIDNEY CAMRAS
Chicago, Illinois
Examination of the Conopidae of the California Insect Survey,
~ University of California through the courtesy of P. D. Hurd, Jr.,
reveals the following new species from the extreme south and
southeastern part of California.
Zodion californicum Camras, new species
Vertex black; ocelli and vertex at anterior margin of ocellar triangle
brownish. Front, face, and cheeks yellow; the front brighter, and the cheeks
more silvery pollinose. Antennae dark brown, the distal lower half of the
166 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
second segment yellowish. Second segment about 3 X length of the retracted
first segment. Third segment about one-half length of second. Arista black.
Proboscis black, about 1 1/3 X head height. Occiput gray.
Thorax gray pollinose with narrow black median line. Faint narrow
submedian lines present anteriorly. Sublateral lines fused with lateral spots,
making dorsum of thorax predominently black. Scutellum with six marginal
bristles. Legs gray with yellowish at apices of femora and bases of tibiae.
Proximal tarsal segments brownish, distal segments black. Pulvilli and claws
yellow; tips of claws black. Wings hyaline, suffused with dusky. Calypters
whitish; halteres yellowish. First posterior cell open. Abdomen gray pollinose,
first segment blackish dorsally. Second and third segments with dorsal tri-
angular black marks pointing anteriorly, and black marks anterolaterally,
giving the pollinose areas an oblique pattern. Fourth segment with two dark
marks distally. Fifth and sixth segments with narrow black transverse lines
at base, and sixth segment with similar line at apical margin. Genital seg-
ments shining black. Genital plate very short and thick. Size 8¥% mm.
Holotype 2: Catirornia: RipLey, RrversipE County, 26. VI.
46, W. F. Barr, (sweeping alfalfa), University of California Collec-
tion. Deposited in the California Academy of Sciences. Paratype 9
California: Blythe, Riverside County, 22. VI. 46, W. F. Barr (Uni-
versity of California). Similar to holotype, but black areas darker
and slightly more extensive, especially on the antennae. Size 7.5
mm. Paratype 9. California: Ripley, Riverside County, 2. VII. 46,
W. F. Barr (author’s collection). Similar to holotype, but black
areas paler. Vertex and dark areas on proximal segments of abdo-
men partly brownish. Size 8.5 mm. Paratype 9. California: Barrett
Springs, San Diego County, 20. IV. 50, J. W. MacSwain (University
of California). Similar to holotype, but dark areas paler, antennae
and front slightly rufous. Second and third antennal segments equal.
Cheeks very large, equal to eye height. Lateral spots on thorax nearly
absent leaving dorsum of thorax predominantly gray pollinose.
Legs predominantly black. Distal abdominal segments more black,
less pollinose. Proboscis longer, about one and two-thirds x head
height. Size 9 mm. ;
This species is related to obliquefasciatum differing by the
complete absence of any rufous coloration. From cyanescens it
differs immediately by the absence of bluish coloration, and from
albonotatum by the lack of yellow pollen and different pattern of
the abdomen.
LITERATURE CITED
Camras, S. |
1943. Notes on the North American Species of the Zodion Oblique-
fasciatum Group. Entomological News 54:187-191.
JuLy, 1954] JEWETT—STONEFLIES 167
NEW STONEFLIES FROM CALIFORNIA AND OREGON
(Plecoptera )
STANLEY G. JEWETT, JR.
7742 S, E, 27th Avenue, Portland, Oregon
In studying a large number of stoneflies from western North
America, collected by the writer and others, several new species
have been found, the sexes have been associated for several species,
and it seems necessary to propose new generic or subgeneric
names for certain forms. Fourteen such species, of which eight
are new, are treated below.
The writer is indebted to Dr. E. S. Ross, California Academy
of Sciences, Dr. Robert L. Usinger, University of California, and
to Mr. Harry P. Chandler, California Fish and Game Department,
for sending material upon which a part of this paper is based.
PELTOPERLA (SOLIPERLA) THYRA Needham and Smith
1916. Peltoperla thyra Needham and Smith, Can. Ent., 48:87, male.
1925. Peltoperla thyra Needham and Claassen, Monog. Plecop., pp. 170-171.
1952. Peltoperla (Soliperla) thyra Ricker, Syst. Studies Plecop., p. 157,
placed in new subgenus Soliperla.
Among material of Soliperla from the collection of the California
Academy of Sciences are two males and five females which are considered to
be specifically identical with the type of P. thyra from Nevada. Dr. Henry
Dietrich of Cornell University kindly loaned the type of thyra for examination,
and it agrees with the males from California in all details except that the
sclerotized structure of the aedeagus in ventral view appears to be composed
of a single pair of smooth-surfaced appendages, divergent at the tips and
tapering to sharp points, whereas the California males have a small pointed
spine or tooth midway between the base and tip of each long appendage. The
ninth segment of the type of thyra is mounted on a slide, and the details of
the aedeagal structure are not clearly visible; auxillary spines may be present
but are not readily seen.
Female.—In general features similar to the male except for slightly larger
size. The subgenital plate is produced over the ninth sternite and is very
similar to that of P. campanula, described below, but is perhaps somewhat
shorter in length.
Allotype female — 6 MILES souTH OF MippLETowN, LAKE
County, Cattrornia, May 12, 1926, deposited in the collection of
the California Academy of Sciences. A male and four additional
females were taken with the allotype, and an additional male was
collected the day before, May 11, 1926, at the same locality.
Peltoperla (Soliperla) campanula Jewett, new species
Length to wing tips: male 16-17 mm.; female 18-20 mm. Length of
body: male 11-12 mm.; female 13—14 mm.
General color dull yellowish brown. Head short, not as wide at compound
168 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
eyes as posterior width of pronotum but as wide as the anterior border. Head
yellowish with a dark area between and anterior to the ocelli. Distance
between ocelli about the same as distance of either to compound eye. Pro-
notum with a median, somewhat irregular brown stripe; discs yellowish with
dark brown rugosities; not quite twice as wide as long, front angles sharp,
hind angles broadly rounded. Mesonotum and metanotum brown. Wings not
infuscated. Dorsum-of abdomen yellowish-brown. Legs brownish dorsally,
yellowish-brown ventrally. Antennae and cerci light brown. Cerci with 13 to
15 segments, the basal segment being about as long as the combined length
of next three. Two pairs of thoracic gills present, one each on the sides of
the meso- and metathorax above and slightly behind the coxae. Each gill is
a single thick filiment at most about two and one half times as long as wide.
Cervical gills absent. ;
Male.—Ninth abdominal sternite bearing a median, slightly raised
transverse lobe behind which there, is a depressed U-shaped area, distal
portion of which is upturned and broadly rounded; ninth tergite unmodified ;
supra-anal process short and recurved with a heavily sclerotized median
structure that is expanded at distal end and bears a row of short teeth
across lower edge of front margin (fig. 1B); in dorsal view this structure
is widely expanded at distal end (fig. 1A); a flap-like membranous structure
lies at either side of median structure as in (fig. 1). Aedeagus in shape of
large membranous sac bearing two irregular rows of short sclerotized spinules
on its ventral surface (fig. 1C), these usually visible through wall of ninth
sternite when aedeagus is in retracted, normal position; dorsally near base
are two small mebranous lobes at either side, each bearing a short, slender
spine; tenth segment narrow; tergite about one-fourth as wide as that of
eighth segment, sternite about a third that of eighth segment.
Female.—Similar in general features to male but somewhat larger. Sub-
genital plate produced over ninth sternite and broadly rounded, without a
notch, about twice as long as seventh sternite (fig. 1D).
Nymph.—A mature nymph taken at the same locality on the same date
as the holotype is described as follows: Length of body: 13 mm. Body brown,
roach-like, covered with fine light hairs. External gills as described above
for adult. Stout spines or bristles distributed as follows: on all borders of
pronotum with those on front margin longest, and in a small patch near
middle of rear margin; in a transverse row across middle of mesonotum and
metanotum; scattered on wing covers and on their outer and posterior
borders, with a prominent patch near posterior margin of each cover; as a
fringe around entire margin of anterior ventral plate of thorax, and on sides
and posterior margins of other two plates; as a fringe completely around hind
margin of each abdominal segment; as a fringe around each of twenty-four
segments of right cercus (some segments of left cercus missing) ; on subanal
lobes; a row each on anterior and posterior outer margins of coxae; a row
on posterior outer margin of trochanter; along upper and lower outer margins
of femur and in a terminal band; in three longitudinal rows and terminal band
on tibia. The femur is deeply grooved below on its outer end to hold the
tibia when folded. Each sternum of thorax with a plate overlapping back-
wards (fig. 1E).
guty, 1954] JEWETT—STONEFLIES 169
The mouthparts differ from described nymphs of other Peltoperlae from
western North America. Galea much exceeding the lacinia, with a tuft of
hairs at the tip (fig. 1G); lacinia with a broad blunt tip that is somewhat
excavated ventrally and with no inner spines; paraglossae curved and slightly
longer than the glossae (fig. 1F), without a small segment at the tip; ~
mandibles with a few wedge-shaped teeth and a curved hard surface behind
them.
Holotype male and allotype female—OxsBow Sprincs, Hoop
River County, Orecon, May 19, 1940, 5. G. Jewett, Jr. Paratypes,
all from Oregon, as follows: same data as for holotype and allotype,
ten males, one female; same data except April 18, 1940, two males;
same data except May 26, 1940, six males, three females; Wah-
keena Falls, Multnomah County, May 3, 1947, S. G. Jewett, Jr.,
seven males, two females (one pair in copula) ; Silver Creek Falls,
Marion County, July 14, 1934, J. Schuh (Illinois Natural History
Survey collection), one male; same locality except August 2, 1948,
K. M. Fender, one male, one female; Hood River Meadows, Hood
River County, July 18, 1947, K. M. Fender, one male. Holotype
and allotype deposited in the collection of the California Academy
of Sciences. Paratypes deposited in the collections of the
following: the writer, Wm. E. Ricker, California Academy of
Sciences, Cornell University, and the Illinois Natural History
Survey. ; :
This new species is close to Peltoperla (Soliperla) thyra Need-
ham and Smith, but is readily separated from that species in having
an unmodified ninth tergite and in details of the male genitalia,
in particular the row of small sclerotized spinules of the aedeagus.
Peltoperla (Soliperla) quadrispinula Jewett, new species
Generally similar to P. campanula, described above, in size
and color.
Male—Ninth abdominal sternite with a lobe similar in size and shape
to that of P. campanula, and the shape of the sternite is much as in that
species; ninth tergite shallowly excavated on hind margin as described for
P. thyra. Supra-anal process very similar to that of P. campanula in size and
shape. Aedeagus bears two pairs of long, sclerotized spines (fig. 2), which
can usually be seen through wall of ninth sternite when aedeagus is in re-
tracted, normal position. Tenth segment similar to that of P. campanula.
Female—Subgenital plate is produced over ninth sternite and broadly
rounded as in P. campanula and P. thyra, and on the basis of available
material cannot with certainty be separated from these species.
Holotype male and allotype female: WRANcGLE Gap Camp,
Rogue River NationaL Forest, Jackson County, Orecon, Aug-
170 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXX, NO. 3
ust 11, 1950, K. M. Fender. Paratypes as follows: same data as for
holotype and allotype, one male; Coffee Creek, Trinity County,
California, June 7, 1934, E. C. Van Dyke, one male. Holotype and
allotype deposited in the collection of the California Academy of
Sciences. Paratypes deposited in the collections of the writer and
the California Academy of Sciences. :
In addition to the above material, the writer’s collection con-
tains a male and a female of this species from a small tributary of
Big Creek, Clatsop County, Oregon, taken by him May 28, 1949;
these specimens are excluded from the paratypic series because
the aedeagus of the male has been lost.
This new species is readily distinguished from allied species
in the male by the sclerotized spiny structures in the aedeagus and
is separated from P. companula by the slightly depressed: posterior
portion of the ninth tergite.
Sierraperla Jewett, new subgenus
Study of both adult and nymphal material of Peltoperla cora
Needham and Smith reveals that the shape and location of the gills
are different from those of species of the subgenus Yoraperla
Ricker or other described subgenera of Peltoperla, and the nymph
differs in additional details. It is therefore felt necessary to propose
a new monotypic subgenus for the species cora, a description of
the nymph of which follows.
Type of subgenus: Peltoperla cora Needham and Smith.
PELTOPERLA (SIERRAPERLA) CORA Needham and Smith
1916. Peltoperla cora Needham and Smith, Can Ent., 48:86, male and female.
1925. Peltoperla cora Needham and Claassen, Monog. Plecop. pp. 172-173.
1952. Peltoperla (Yoraperla) cora Ricker, Syst. Studies Plecop., p. 157,
placed in new subgenus Yoraperla.
A nearly mature nymph from Howell’s, Plumas County, Cali-
fornia, collected August 29, 1946, by Harry P. Chandler, is
described as follows:
Length of body 13 mm. Body brown, some fine, pilose hairs on body but
general appearance is smooth, roach-like in aspect although less so than are
species of the subgenus Yoraperla. Stout spines or bristles distributed as
follows: at outer anterior and posterior corners of pronotum; on lateral and
hind margins of the mesonotal and metanotal wing covers (sparse on this
specimen which may not be typical in this respect); on lateral margins of
head below compound eyes; as a border completely around hind margin of
last three abdominal segments, as a border across sterna of next three seg-
juLy, 1954] JEWETT—STONEFLIES 171
ments, absent or nearly so on first three segments; as a fringe around anter-
ior border of twenty-one segments of the cercus. (distal segment or more
missing) ; on subanal lobes; on the outer borders of coxae; on outer border
of trochanter; on sides and distal end of outer face of flattened femur; on
sides and distal end of outer face of little-flattened tibia. Femur grooved
below, tibia capable of folding back along its inner, lower margin; sternal
plates overlapping posteriorly (fig. 3). One pair of external gills, finger-like,
in cervical region; two gills, one above the other and posterior to each coxae
of prothorax and mesothorax; and one gill behind each coxae on the meta-
thorax in the position of upper gills on prothorax and mesothorax. Upper
gills on each segment bilobed, forming a T, the arms extending dorsad and
ventrad; a basal stub or short lobe present on lower gill of prothorax and
mesothorax; all gills robust. Posterior portion of terminal abdominal tergite
of nymph greatly extended posteriorly and upturned to a pointed tip, re-
sembling that of some species of Pteronarcys. Galea about equal to lacinia
in length, tip turned slightly outward and with a tuft of fine hairs (fig. 3B) ;
lacinia with an outer and inner tooth, tips of both chisel-shaped; paraglossae
slightly curved, and only a little longer than glossae (fig. 3A).
Nemoura wahkeena Jewett, new species
Length to end of body: male 4 mm.; female 4-5 mm.; both sexes
brachypterous. General color light brown. Four cervical gills, each composed
of two compressed filaments which are branched once or twice beyond the
base; length of each gill about six times its width at the base. Head wider
than pronotum, dark brown except for a paler area beyond the anterior
ocellus. Pronotum about as wide as long, narrowed in width posteriorly and
with the angles broadly rounded, generally dark with light lateral and pos-
terior margins. Forewing reaching to about the middle of the metanotum,
hind wings slightly shorter. Antennae composed of 27-32 segments, equal
to or slightly greater than the length of body.
Male—Abdominal segments brown, the eighth, ninth, and tenth most
heavily sclerotized; ninth tergite posteriorly with wide crescentic membran-
ous area; ninth sternite greatly produced behind and with a lobe. Cerci
small, curved, sclerotized on outer faces, concave and membranous on inner
faces, tipped with a tiny robust spine. Supra-anal process recurved, and
from above, widest in the middle as in (fig. 4), membranous dorsally, sclero-
tized ventrally. Subanal lobes double, an inner strongly sclerotized lobe which
ends in a tapered, outwardly-directed point and an outer lobe which
is membranous.
Female—In general features similar to male. Cerci are unmodified.
Seventh sternite bulbous, membranous, extending over anterior half of eighth
sternite (fig. 4B); eighth sternite largely sclerotized, on posterior median
margin is visible a strongly sclerotized narrow ring surrounding oviduct;
ninth sternite is largely sclerotized, tenth, only slightly so.
Holotype male and allotype female, taken in copula: WAHKEENA
Fats, MuttNomaH County, Orecon, April 5, 1947, S. G. Jewett,
Jr. Paratypes: three males, five females, including a pair in copula,
same data as for holotype and allotype. Holotype and allotype
72 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 3
deposited in the collection of the California Academy of Sciences.
Paratypes deposited in the collections of the writer, Wm. E. Ricker,
and the Illinois Natural History Survey.
This distinctive small species can be readily separated from
described species. of Nemoura by the extreme brachyptery of both
sexes, by the shape of the gills, and by the distinctive subanal lobes
of the male. The male supra-anal process, particularly its expanded
middle portion in dorsal view, also distinguishes it from described
males of the subgenus Zapada Ricker to which it is tentatively
assigned.
Nemoura spiniloba Jewett, new species
Male—Length to end of body: 6 mm. Length to wing tips: 8 mm. Gen-
eral color brown. No external gills in male holotype. Head dark brown, wider
than pronotum; pronotum generally dark in color, wider than long, narrowed
posteriorly with anterior angles rather sharp, posterior angles broadly
rounded; wings normal. Antennae with more than fourteen segments, second
segment smaller than large basal segment, about one-half as long as third
segment. Abdominal segments brown, first eight without significant sclerotiz-
ation, ninth and tenth segments wholly sclerotized; ninth sternite produced
posteriorly into a lobe and with the usual lobe from its anterior margin (fig.
5A), Cerci sclerotized, a tiny spine at tip. Supra-anal process recurved to pos-
terior border of tenth tergite, wider than deep, and with a slightly enlarged tip
from above and from the side, more heavily sclerotized ventrally than dor-
sally (fig. 5). Subanal lobes broad at base, quadrangular, and with a slender
acute process developed from the inner margin (fig. 5A).
Holotype male: WoopacreE, Marin County, Catirornia, March
31, 1949, L. W. Quate. Deposited in the collection of the California
Academy of Sciences.
The genitalia of this new species resemble those of NV. cataractae
Neave but are readily separated by the shape of the cerci and
subanal lobes. Should additional material agree with the holotype
in lacking gills on the mentum or in the cervical region, it may
become advisable to erect a new subgenus for this species. The
holotype was a pinned specimen which has been relaxed and
preserved in alcohol.
EXPLANATION OF FIGURES
Fig. 1. Peltoperla (Soliperla) campanula, male genitalia, lateral aspect;
1A, supra-anal process, from above; 1B, supra-anal process, distal end from
below; 1C, aedeagus extruded, ventral aspect; 1D, female subgenital plate;
1E, sternal plates of nymph; 1F, labium of nymph; 1G, maxilla of nymph.
juLy, 1954] JEWETT—STONEFLIES ps
Fig. 2. Peltoperla (Soliperla) quadrispinula, male genitalia, aedeagal structure
through ninth sternite. Fig. 3. Peltoperla (Sierraperla) cora, sternal plates of
nymph; 3A, labium of nymph; 3B, maxilla of nymph. Fig. 4. Nemoura wah-
keena, male genitalia, dorsal aspect; 4A, male genitalia, ventral aspect; 4B,
terminal sternites of female. Fig. 5. Nemoura spiniloba, male genitalia, dorsal
aspect; 5A, male genitalia, ventral aspect. Fig. 6. Capnia californica, eighth
sternite of female.
174 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
Capnia maculata Jewett, new species
Length to wing tips: male holotype 9 mm.; female allotype 11 mm.
Length of body: male holotype 7.5 mm.; female allotype 8 mm.
General color in alcohol brown. Head through compound eyes wider
than pronotum; lateral ocelli about twice as far apart as distance from
inner margins of compound eyes; median ocellus about as far forward from
lateral ocelli as distance between them. Pronotum slightly wider than long, with
a distinct median logitudinal line, embossed. Venation of wings typical, with
R, bent upward at its origin and with A; bent abruptly caudad at its junction
with cu-a and then curved outwardly again. Wings conspicuously spotted, par-
ticularly on the outer half of the forewing and the radial area of the hind
wing. :
Male—First eight abdominal segments without special structures; ninth
sternite with a prominent lobe at base (fig. 7). Subanal lobes fused distally
to form a slender, sharp point. Ninth tergite with a pair of heavily sclerotized
knobs on anterior half of sclerite. Supra-anal process of tenth tergite almost
square in cross-section, recurved, with blunt tip resting between knobs of
ninth tergite. Cerci long, many-segmented.
Female—Eighth abdominal sternite (fig. 7A), with a subgenital plate
which occupies central part of sternite, distal portion of which extends well
beyond posterior margin of segment. A broad median membranous stripe ex-
tends longitudinally across tergites one through eight.
Holotype male: MarsH Creek, Contra Costa County, Catt-
FoRNIA, March 6, 1950, L. W. Quate. Allotype female; Colorado
Creek and Mines Road, Santa Clara County, California, April 6,
1949, Ray F. Smith. Paratype female: Livermore, Alameda County,
California, March 31, 1929, E. C. Van Dyke. Holotype and allotype
deposited in the collection of the California Academy of Sciences,
the paratype deposited in the writer’s collection.
This new species differs from all previously described North
American species of Capnia in having spotted wings and in
possessing a ventral appendage on the ninth sternite of the male.
It bears resemblance to such Asiatic species as C. cordata Kimmins
which has “faint smoky clouds” in the apical half of the wings,
a bifurcate knob on the ninth tergite, and a ventral lobe on the
ninth sternite. ,
Capnia licina Jewett, new species
Male—Similar in general morphological details to other species of the
genus Capnia. Length to wing tips: 6 mm. Length of body: 5.5 mm.
General color brown, wings hyaline. First six abdominal tergites without
special structures; seventh, eighth, and ninth, tergites (fig. 8), with median
raised tubercles, that of eighth most prominent; tenth tergite notched medi-
ally; membranous areas present on seventh and eighth tergites behind tuber-
juny, 1954] JEWETT—STONEFLIES 175
cles and anterior to tubercle on ninth tergite. Supra-anal process reflexed,
tip upturned and nearly reaching posterior margin of eighth tergite; length
of supra-anal process equal to 8 to 10 times its diameter at middle.
Holotype male: SMALL CREEK AT THE JUNCTION OF OREGON
HIGHWAYS NUMBERS 36 AND 50, CLackKAMAS CouNTY, OREGON, —
April 22, 1948, S. G. Jewett, Jr. Deposited in the collection of the
writer.
This species differs from other described species of North
American Capnia in possessing both tubercles on tergites 7 to 9
and a reflexed supra-anal process with the tip upturned. The length
of the process is less than that of other species where the tip is
upturned.
CAPNIA CALIFORNICA Claassen
1924. Capnia californica Claassen, Can. Ent., 56:57, male.
1925. Capnia californica Needham and Claassen, Monog. Plecop., pp. 262-
263.
Female—Similar in general morphological details to male. Length to
wing tips: 8 mm. Length of body: 6-7 mm.
Eighth abdominal sternite (fig. 6), with subgenital plate well developed,
sclerotized as in figure 6, not fused with seventh sternite; distal end of plate
is bordered by a heavily-sclerotized band; membranous area on eighth stern-
ite varies in shape, almost triangular to crescentic; usual, broad, membranous
median stripe extends longitudinally across the first eight tergites.
Allotype female—A small creek near Saratoga, Santa Clara
County, California, February 25, 1940, S. G. Jewett, Jr. Allotype
deposited in the collection of the California Academy of Sciences.
With the allotype six additional females and seven males were
taken.
CAPNIA OREGONA Frison
1942. Capnia oregona Frison, Pan-Pac. Ent., 18:2, pp. 63-64, male.
Female—In general features similar to male, both sexes having wings
uniformly stained with brown. Eighth abdominal sternite with a subgenital
plate as in figure 9; a dark brown pigmented area occurs on either side of
central, distal portion of sternite, and additional pigmented patches occur
on ninth sternite in comparable areas; usual broad median stripe occurs
longitudinally across first eight tergites.
Allotype female—Benton County, Oregon, 14 miles south of
Corvallis, Muddy Creek, February 10, 1938, S. G. Jewett, Jr.
Deposited in the collection of the California Academy of Sciences.
The allotype was taken with the holotype and several other
specimens of this species, but Frison apparently failed to note the
distinctive wing color of this species and consequently did not
associate the sexes.
176 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXX, NO. 3
Rickera Jewett, new genus
This: genus, erected for the new species described below, is
tentatively placed in the Isoperlinae because in the male the tenth
tergite is entire, and the male subanal lobes resemble those of some
species of /soperla. The head and thorax color pattern, thé shape
of the female subgenital plate, and the lobe on the seventh sternite
of the male strongly suggest Isogenus in the subfamily Isogeninae
as defined by Ricker (1952).
Type of genus: Rickera venusta Jewett.
Rickera venusta Jewett, new species
Length to wing tips: male 17-18 mm.; female 20 mm. Length of body:
male 12 -14 mm.; female 14-16 mm. General color gray-brown with yellow
markings on head and thorax and with fumose wines.
Head at compound eyes slightly wider than prothorax, mostly yellow
within ocellar triangle, a large yellow spot anterior to forward ocellus, head
yellow behind posterior ocelli except for brownish areas on either side be-
hind the compound eyes. Prothorax with a wide, central yellow band which
diffuses into lateral brownish areas, stripe occupying one-fourth to one-third
of prothoracic width; prothorax distinctly wider than long, both anterior
and posterior angles rounded. First tarsal segment about twice as long as
second, the third, two or three times as long as the first and second combined.
Wings fumose; subcosta not reaching the cord; a series of several costal
crossveins before end of subcosta and two or three beyond in both fore
and hind wings; radial sector forked twice beyond the cord. Abdomen with a
narrow, median, dorsal stripe that extends across first eight tergites.
Male—Subanal lobes (fig. 10) erect, mostly membranous. No supra-anal
process. A lobe with an uneven distal margin is present on posterior margin
of seventh sternite fig. 10A).
Female—Subgenital plate (fig. 10B) wide, extending across anterior
half of ninth sternite, its. tip broadly rounded.
Holotype male and allotype female: Rocue River aT Murr
CREEK, JACKSON County, OrEGOoN, June 17, 1949, S. G. Jewett, Jr.
Paratypes as follows: Rogue River at Foster Creek, Jackson
County, Oregon, June 17, 1949, S. G. Jewett, Jr., two females; Clear
Creek, Wasco County, Oregon, June 19, 1952, S. G. Jewett, Jr.,
one male; Olallie Creek Forest Camp, McKenzie River, Lane
County, Oregon, July 15, 1952,S. G. Jewett, Jr., one male. Holotype
and allotype deposited in the collection of the California Academy
of Sciences. Paratypes are in the collections of the writer and Wm.
FE. Ricker.
This new genus is named in honor of Dr. Wm. E. Ricker who
has done so much on the taxonomy and phylogeny of Plecoptera.
JULY, 1954] _ JEWETT—STONEFLIES 177
10s
2B
eet ee 13a
EXPLANATION OF FIGURES
Fig. 7. Capnia maculata, male genitalia, lateral aspect; 7A, eighth ster-
nite of female. Fig. 8. Capnia licina, male genitalia, lateral aspect. Fig. 9.
Capnia oregona, eighth sternite of female. Fig. 10. Rickera venusta, male
genitalia, lateral aspect; 10A, lobe on male seventh sternite; 10B, terminal
sternites of female. Fig. 11. Isogenus (Kogotus) alameda, terminal sternites of
female. Fig. 12. Isoperla marmorata, male genitalia, lateral aspect; 12A, two
examples of aedeagal structure; 12B, lobe on male eighth sternite. Fig. 13.
Alloperla (Alloperla) chandleri, male genitalia, lateral aspect; 13A, eighth
sternite of female.
178 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
IsoceNnus (Kocotrus) ALAMEDA (Needham and Claassen)
1925. Perla alameda Needham and Claassen, Monog. Plecop., pp. 78-79, male.
1952. Isogenus alameda Ricker, Syst. Studies Plecop., p. 128, placed in
Isogenus and suggested as belonging in Kogotus.
Female—Subgenital plate occupies middle half of eighth sternite and
extends posteriorly to anterior margin of tenth sternite, broadly rounded
with or without a wide shallow emargination (fig. 11).
Allotype female——Pinnacles National Monument, San Benito
County, California, May 3, 1946, H. P. Chandler. Deposited in the
collection of the California Academy of Sciences.
This species is assigned to the subgenus Kogotus Ricker (1952)
because the tip of the anterior band is coiled inside of the supra-
anal process. The paragenital plates are produced upward into
rounded, spinulose tips.
Since this species has been recorded only from San Antonio
Creek, Alameda County, the following additional California records
are listed: Same as allotype, one male; Lake Curry, Solano City,
Lake County, April 13, 1950, J. N. Simons, one male; Livermore,
Alameda County, May 11, 1930, E. C. Van Dyke, three males, one
female; Pope Valley, Napa County, May 8, 1930, E. C. Van Dyke,
two females; Livermore, April 30, 1928, one female.
ISOPERLA MARMORATA (Needham and Claassen)
1925. Clioperla marmorata Needham and Claassen, Monog. Plecop., pp. 142-
143, female.
Male—Generally similar in morphological details to female but some-
what smaller in size. Subanal lobes cylindrical, recurved, and bluntly tipped
(fig. 12). Eighth sternite with a shallow, broadly rounded lobe on posterior
portion (fig. 12B) which does not extend beyond end of segment. Aedeagus
with a sclerotized, translucent process, blade-like at distal end, teardrop
shaped in lateral view (fig. 12A); in some specimens base of process is
finger-like, in others it appears to taper rapidly to a blunt, rounded end.
Marmorata differs from described species of Isoperla from
western North America in having the anal area of the hind wings.
fumose, sometimes lightly so, sometimes more heavily, as in the
holotype. The head color pattern as described for the holotype, the
cylindrical subanal lobes of the male, and the scarcely extended
subgenital plate of the female also differentiate it from described
species.
Allotype male—Eagle Creek, Clackamas County, Oregon, April
16, 1940, S. G. Jewett, Jr. Deposited in the collection of the Cali-
fornia Academy of Sciences.
The following additional material of this species has been ex-
JULY, 1954] ZOOLOGICAL NOMENCLATURE 179
amined: Same data as for allotype: seven males, one female; same
data except May 5, 1940, two males, five females; same data except
June 27, 1948, one male; Soap Creek, Benton County, Oregon,
May 24, 1947, E. Holmberg, one male; 3 miles south Camino,
Eldorado County, California, June 26, 1948, D. Carter, two males,
two females; Middletown, Lake County, California, May 11, 1926,
three males; tributaries of Smith Creek, elevation about 5,000 feet,
Blairsden, Plumas County, California, June 11, 1952, Wm. E.
Ricker, one male, one female, one exuvia.
Alloperla (Alloperla) chandleri Jewett, new species
Male—Typical in color for members of the subgenus Alloperla, without
dark markings on head, thorax, or abdominal segments, presumably greenish
in life. Supra-anal process (fig. 13) membranous basally with anterior sclero-
tized portion bent forward and hinged so that it can be moved vertically on
its attachment with membranous basal portion; tip of process is flat in end
view; dorsally process is slightly dumbbell-shaped.
Female—Subgenital plate (fig. 13A) slopes caudally abruptly towards
its center to form a pointed process which reaches anterior border of ninth
sternite.
Holotype male, allotype female, two male paratypes, and one
female paratype: 6 MILES EAST OF Miami RANGER STATION, ELE-
VATION 6,000 FEET, Mariposa County, Catirornia, July 4, 1946,
Harry P. Chandler. Holotype and allotype deposited in the col-
lection of the California Academy of Sciences, paratypes in the
collections of H. P. Chandler and the writer.
This new species differs from other described species of Allo-
perla proper, from western North America in the shape of the
male supra-anal process. From. A. elevata Frison, to which it bears
some resemblance, chandleri is readily separated by the thickness
of the tip of the supra-anal process which is about as deep as
broad whereas in elevata it is quite thin in lateral view.
ZOOLOGICAL NOMENCLATURE: Notice Or Proposep Sus-
PENSION Or THe Rutes In Certain Cases For THE AVOIDANCE
Or ConFusion AND THE VALIDATION OF CURRENT
NOMENCLATORIAL Practice (A. [n.s.] 18)
Notice is hereby given that the possible use by the International
Commission on Zoological Nomenclature of its Plenary Powers is
involved in applications relating to the under-mentioned names.
180 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
Under the decision by the International Congress of Zoology
the period within which comments on the applications covered
by the present Notice are receivable is a period of six calendar
months calculated from the date of publication of the revelant
Part of the Bulletin of Zoological Nomenclature.
(1) Applications in Part 6 of Vol. 9
(1) immigrans Sturtevant, 1921, as published in the combination Droso-
phila immigrans (Class Insecta, Order Diptera), proposed validation
of (pp. 161-162) (File Z.N. [S.] 711).
(2) pruni Geoffroy, 1762, as published in the combination Aphis pruni
(Class Insecta, Order Hemiptera), proposed validation of (pp. 163-
165) (File Z.N. [S.] 428).
(3) Lachnus Burmeister, 1835, and Cinara Westwood, 1835, proposed de-
signation of type species for, in harmony with accustomed usage
(Class Insecta, Order Hemiptera) (pp. 174-183) File Z.N. [S.] 174).
(2) Applications in Part 7 of Vol. 9
(4) Stentor Oken, 1815(Class Ciliophora), proposed validation of, and
designation of a type species in harmony with accustomed usage
(pp. 208-213) (File Z. N. [S.] 261).
(5) Melanargia Meigen, 1828 (Class Insecta, Order Lepidoptera), pro-
posed validation of (pp. 221-222) (File Z. N. [S.] 708).
(3) Applications in Part 8 of Vol. 9
(6) Geoffroy, 1762, Historie Abregee des insectes qui se trowvent aux en-
virons de Paris, proposed validation of the following six names pub-
lished in, for genera of the Order Diptera: Stratiomys, Stomoxys,
Volucella, Nemotelus, Scatopse, Bibio (pp. 241-246) (File Z. N. [S.]
710).
(7) Palmatotriton Smith, 1945 (Class Amphibia), proposed suppression
of (pp. 247-249) (File Z.N. [S.] 594).
(8) Ammonites mammillatus Schlotheim, 1813, proposed designation of
a neotype for, and Douvilleiceras de Grossouvre, 1893 (Class Cephalo-
poda, Order Ammonoidea), proposed designation of a type species
for (pp. 250-254) (File Z.N. [S.] 631).
Any specialist who may desire to comment on any of the fore-
going applications is invited to do so in writing to the Secretary
to the International Commission (Address: 28 Park Village East,
Regent’s Park, London, N.W. 1, England) as soon as possible.
Every such comment should be clearly marked with the Com-
mission’s File Number as given in the present Notice —FRANCIS
HEMMING, Secretary to the International Commission on Zoological
Nomenclature.
juLy, 1954] BoUDREAUX—TETRANYCHID MITES 18]
NEW SPECIES OF TETRANYCHID MITES"
(Acarina)
H. Bruce BoupREAUX
Department of Zoology, Physiology and Entomology, Louisiana State
University, Baton Rouge.
The aid given by Dr. A. E. Pritchard and Dr. E. A. McGregor
in encouragement and study of mite sepcimens from Louisiana is
gratefully acknowledged. The following new species were dis-
covered in the course of this investigation.
Tetranychus merganser Boudreaux, new species
Tetranychus merganser resembles most T. tumidus Banks and
T. atlanticus McGregor. It differs from twmidus in lacking the large
empodial spur and in having the aedeagus terminating in a rather
large distal knob, shaped very much like the head of a merganser
duck. From atlanticus it differs in being red instead of greenish,
and in having a more prominent empodial spur. The aedeagus
terminates in a large distal knob, rounded anteriorly and above,
and the bend of the shaft closely approaches an angle of 90°,
while in atlanticus the bend of the external shaft is usually 60°,
and the distal knob is smaller with the upper surface very broadly
angulate. The empodial spurs of atlanticus are quite obscure.
Female——Palpus with terminal sensillum about twice as long as wide.
Stylophore rounded mediodistally. Peritreme chambered, hooked distally,
chamber at bend of hook often with a swelling. Tarsus I bearing 4 or 5
tactile setae and one sensory seta proximad of but in vicinity of proximal
duplex setae; empodial spur rudimentary; a very tiny bristle usually visible
below the three pairs of proximo-ventral hairs. Dorsum between inner lum-
bar and inner sacral setae with striae transverse and surrounded by a rhom-
boidal area of striae; striations longitudinal between both inner lumbar and
both inner sacral setae. Dorsal setae slender, tapering, weakly pilose and
longer than intervals between them. Length of body from posterior end to tip
of rostrum 0.54, mm.
Male—Palpus with terminal sensillum slender, about three times as
long as thick. Aedeagus with proximal portion of external shaft parallel
sided, narrowing abruptly downward and curving smoothly upward distally,
terminating in a large distal knob whose anterior projection is broadly
rounded, and whose posterior projection forms a sharp beak; upper surface
of distal knob smoothly rounded. Length of body 0.45 mm.
ae
1 This paper has resulted from a study partly supported by a grant from the
Freeport Sulphur Company, and partly by the Louisiana Agricultural Experiment
Station at Baton Rouge.
182 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
Holotype—Male, Baton Rouce, Louisiana, July 7, 1953 (L. D.
Newsom) on Ligustrum vulgare L.; type No. 2172 in U. S. Na-
tional Museum. Morphotye—Female, same data as holotype; type
deposited in U. S. National Museum. Paratypes—Six males and
thirty-six females, all from Ligustrum vulgare, in collection of the
writer. Localities—Monroe, Shreveport, Baton Rouge and Natchi-
toches, Louisiana.
This mite is carmine, with lateral dark spots extending to the
posterior end in older females. Very little web is produced, but
the leaves show signs of injury in becoming spotted with yellow
where a colony is established.
Tetranychus cocosinus Boudreaux, new species
Tetranychus cocosinus is nearly identical in morphological
details with T. cocosi (McG.). It differs in having the posterior
angulation of the distal knob of the aedeagus relatively longer than
in cocost, and with the distal knob slightly sigmoid on the upper
surface, the tip bending downward. In addition, the terminal
sensillum of the palpus of the male is four or more times its thick-
ness, broader. at tip, while in cocosi the sensillum is about three
times as long as thick and parallel-sided. The differences in shape
are the same in the females, but the sensillum is shorter than in the
males. 7’. cocosi is described as “pale chestnut red”’ in life and feeds
on the royal palm in California. T. cocosinus is dark purple, nearly
black, and has been collected on Rubus, Rosa, Ulmus and Celtis
(Hackberry) in Louisiana.
Female.—Body from above broadly rounded. Stylophore rounded medio-
distally or very slightly cleft. Terminal sensillum of palpus about twice as
long as thick, broader near tip. Tarsus I bearing 4 tactile setae proximad of
duplex setae; empodial spur rudimentary but obvious. Striations dorsally
between inner lumbar and inner sacral setae as in T. merganser above. Dorsal
setae slender, weakly pilose and longer than intervals between them. Length
of body 0.49 mm.
Male.—Terminal sensillum of palpus slender, one-fourth as thick as long,
tip slightly broadened and angulate. Aedeagus with external shaft broad at
base, weakly tapering to upward bend where it narrows abruptly, and tipped
with a distal knob whose anterior and posterior projections are acute, the
anterior one shorter than the posterior projection, which bends slightly
downward. Distal knob about three-eighths as long as external shaft, with its
axis parallel with upper surface of shaft and its upper surface slightly sig-
moid anteriorly. Length of body 0.34 mm.
juLY, 1954] BoUDREAUX—TETRANYCHID MITES 183
Holotype—Male, Port ALLEN, Loutstana, Aug. 18, 1953, (H.
B. Boudreaux) on Celtis sp.; type No. 2174 in U. S. National
Museum. Paratypes—Nine males and eight females from Rubus
sp., Natchitoches, La., one male from Rubus, Baton Rouge, La.,
two males and four females from Hackberry, Port Allen, Louisiana,
and five males and ten females from Ulmus americanus, Baton
Rouge, Louisiana. In collection of the writer.
PLATE I
Tetranychus merganser. Fig. 1, female, pretarsus 1; Fig. 2, female, tar-
sus I; Fig. 3, female, palpus; Fig. 4, male, palpus; Fig. 5, male, aedeagus
(holotype) ; Fig. 6 and 7, aedeagus, male paratypes.
184, “THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 3
Specimens were taken on Rose, Baton Rouge, but they are
not included in the type series. The original slides were poorly
made, and the specimens were lost in attempting to remount them.
The color in life is dark reddish-purple, some nearly black.
Males paler, as usual. Webbing is produced profusely, and Rubus
leaves are markedly injured.
Tetranychus magnoliae Boudreaux, new species
Tetranychus magnoliae is most closely related to T. tumidus
Banks and T. mexicanus McGregor. All have a prominent empodial
spur above the three pairs of empodial hairs on all tarsi. The only
PLATE II.
Figures 8-13. Tetranychus cocosinus. Fig. 8, female, pretarsus 1; Fig.
9, female, palpus; Fig. 10, male, pretarsus I; Fig. 11, male, aedeagus (holo-
type); Fig. 12, male, aedeagus of paratype; Fig 13, male, palpus.
Figure 14. T. cocosi, aedeagus, male from royal palm, California.
juty, 1954] BoUDREAUX—TETRANYCHID MITES 185
other species with such a spur is 7’. braziliensis McGregor, but the
latter has additional small setae and the structure of the empodium
if different. T. magnoliae males differ from those of T. tumidus
and T’. mexicanus in having a much longer posterior angulation on
the distal knob of the aedeagus.
Female.—Thickness of terminal sensillum of palpus about three-fifths the
length, and its length about the same-as that of the dorsal sensillum. Stylo-
phore rounded anteriorly. Peritreme chambered, and hooked distally. Tarsus
I bearing 4 or 5 setae proximad of the proximal duplex setae; empodial spur
one-half as long as the proximo-ventral empodial hairs; a pair of tiny but
distinct setae ventrally proximad of the base of the six empodial setae (these
tiny setae are easily visible on all tarsi, male and female). Posterior dorsal
striations on hysterosoma as in J. merganser and T. cocosinus. Dorsal setae
long, slender and tapering, longer than intervals between them. Length of
body to tip of rostrum 0.53 mm.
ee a 2: I8.
PLATE III.
Tetranychus magnoliae. Fig. 15, female, palpus; Fig. 16, female, pre-
tarsus I; Fig. 17, male, palpus; Fig. 18, male, pretarsus I; Fig. 19, male
aedeagus.
186 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 3
Male.—Palpus with terminal sensillum slightly longer than twice its
thickness, and slightly longer than the dorsal sensillum. Tarsus I with dorsal
émpodial spur nearly as long as the six proximo-ventral hairs, these not fused
as in most species of Tetranychus, but distinct and separate for most of
their length, the ventral pair much thicker than the other two pairs; a pair
of tiny setae near-the base of. the largest pair of empodial setae, as in all
other tarsi. Aedeagus with external shaft emerging broadly, and tapering
quickly outward as it curves upward; the distal knob with a sharp acute
_ anterior angulation, the posterior angulation acuminate and about six times
as long as the anterior point. Length of body 0.35 mm.
Holotype—Male, Baton Rouce, Louisiana, August 20, 1953.
(H. B. Bordreaux) on Magnolia grandiflora; type no, 2173 in
U. S. National Museum. Paratypes—Nine males and seventeen
females from Magnolia and two males and three females from
Liriodendron tulipifera, all taken in Baton Rouge, Louisiana. In
collection of the writer,
On magnolia this mite spins a profuse web on the upper surface
of the leaves, near the midrib, and causes a distinct discoloration
of the leaves as the colony gets older. Apparently the dense hairy
lower surface of the leaves is not a suitable habitat. On the tulip
tree the mites inhabit both surfaces of the leaves. Usually species
of Tetranychus prefer the lower leaf surface, in contrast to this
species. The living mites are carmine red, with paler legs and
propodosoma. The eggs are unusually large, dark cream colored
and spherical.
TWO NEW DIPTERAN PARASITES OF AUTOGRAPHA
CALIFORNICA
Thirty specimens of Autographa californica Speyer, larvae and
pupae, were obtained on spinach four miles west of Walla Walla,
Walla Walla County, Washington, during the months of October
and November, 1953. Twenty per cent parasitism by two genera
of Larvaevoridae (Tachinidae) was observed. They were Madre-
myta saundersit (Will.) and Achaetoneaura archippivora (Will.),
of which the latter is new for this particular host as far as could be
ascertained. The pupation period of both these flies was observed
to be approximately 16-17 days, the mean being 16.5 days.
The writer is indebted to Curtis W. Sabrosky of the United
States Department of Agriculture for determining the above para-
sites —Don R. SEIDEL.
JuLY, 1954] DENNING—LEPIDOSTOMA 187
NEW SPECIES OF LEPIDOSTOMA
(Trichoptera: Lepidostomatidae )
D. G. DENNING
1684 Oak Park, Walnut Creek, California
The six new species of Lepidostoma described herein will in-
crease the total number of named species known to occur in the
United States and Canada to about 40. Slightly over half of the
described species are found only in western Canada and United
States. As is usual in the Lepidostoma several of these new species
possess some remarkable secondary sexual modifications. Unless
indicated otherwise, types are deposited in the writer’s collection.
PLUVIALE GROUP
One of the new species described, errigena, is a member of the
Pluviale group. The combination of characters setting off this
group from. all others are described.
The Pluviale group is characterized as follows: all males have the en-
tire costal cell reflexed, the anterior portion is very wide and the resultant
pocket is lined with scales. The distribution of scales are usually heaviest
along the margin of the reflexed portion. The claspers, long and slender
throughout, do not terminate in an acute point; the baso-dorsal lobe origin-
ating at base of clasper is single, lacking completely a ventro-lateral lobe;
this lobe is af variable size, but always digitate. The small mesal lobe pres-
ent at the apex of the clasper is of variable size, but always small and
acute. The aedeagus bears a dorsal pair of acuminate rods arising from
near base and generally following the contour of the structure. The first
antennal segment is long and slender but not particularly modified; the
maxillary palpi are modified into an apparent single segment, generally
small, closely appressed to the head and bearing a dense brush of scales.
Legs or spurs not modified.
Characters for differentiating the species are largely confined
to the tenth tergite, and is largely based on the structure of a spur
arising from the lateral or apical margin.
Sexual dimorphism is most pronounced in the reflexed con-
dition of the wing, and as Ross (1946) has pointed out, it is not
limited only to this group. However, no other group has a com-
bination of all the above characters and none possess such a wide
reflexed pocket. Reflexed portions of the subcostal cell from a
mere pocket to three-fourths the length of the cell occurs in several
species not related to the Pluviale group.
The new species, errigena, will increase the members ascribed
to this group to nine. When a series of several species from various
sections of the country was studied it was found that a wide range
of variations existed and suggest that with larger series our concept
188 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
of some of the sepcies may change. It is entirely probable that
when larger series of pluviale, rayneri, veleda, and ormea are
studied we will fiind that only one highly variable species is
involved.
Lepidostoma errigena Denning, new species
This species, a member of the pluvialis group, is probably
closest related to aporna Denning. The prominent dorsal lobe and
the peculiar ventral spur will differentiate this species from others.
Male.—Length 7-8 mm. General color light brown. First antennal seg-
ment long and slender and bearing a dense brush of scales and setae along
mesal margin. Maxillary palpi apparently one segmented, apex appressed
against head and bearing a dense brush of dark brown scales. Front wings
with entire costal cell reflexed, lined with dark brown scales.
Genitalia as in fig. 1. Tenth tergite widely separated on meson and thus
divided into a pair of lateral lobes; ventral margin broadly rounded, the
apico-ventral corner of ventral lobe produced into a ventrad directed spine
and a caudad directed spine which may be bifid or single; dorsal spur
prominent, slender and acute, reaching nearly to level of tergite; dorsal lobe
not produced caudad. Clasper from lateral aspect typical of group—slender,
long, basodorsal lobe digitate; from ventral aspect (fig. 1B) small acute
process near apex along mesal margin. Aedeagus tubular, bearing a pair of
long, closely appressed, very slender acuminate rods.
Holotype male, SEVEN Oaks, SANTA ANA RIVER, SAN BERNAR-
DINO Mrs., SAN BERNARDINO County, CaLirorniA, July 8, 1950,
John Belkin. Paratypes, two males, same data as for holotype; two
males, Palomar Mt., San Diego Conuty, July 12, 1946, 4700’, C. P.
Alexander. Holotype and one paratype deposited in the collection
of the Academy of Science, San Francisco, California.
UNICOLOR GROUP
This group contains the largest number of described species.
These species are quite variable but all possess the following
characteristics. The clasper, while differing among the various
species, is always short, and the baso-dorsal process is also short
and usually pointed at the apex. The front wings have only a narrow
reflexed area or only a small basal portion of the costal cell will
be reflexed. Some of the most remarkable sexual modifications
occur among the males of this group.
Lepidostoma recina Denning, new species
This species is a member of the wnicolor group. It may be
distinguished from other species by the ventral lobe of the tenth
tergite.
Male.—Length 9 mm. Wings, legs and antennae light brown. Front
JULY, 1954] DENNING—-LEPIDOSTOMA 189
wings with reflexed cell wide but covering only about three-quarters of the
costal cell, resultant pocket lined with brownish scales; along cubitus an
infolding of the membrane produces a second distinct pocket in the wing.
Maxillary palpi apparently one segmented, short and flattened, apical portion
bearing a dense brush of blaskish scales. First antennal segment long and
slender, no secondary modifications.
Genitalia as in fig. 2. Tenth tergite as seen from dorsal aspect (fig. 2B),
separated on meson only a short distance, apices of dorsal lobe sub-triangular,
along dorso-mesal portion there is present a row of short protuberances just
discernable, each bearing a short seta; along lateral margin there is a series
of several prominent spines each bearing a short seta; ventral lobe produced
caudad beyond remainder, truncate and serrate, lateral margin sinuate. Tenth
tergite from lateral aspect (fig. 2A) with ventral margin arcuate, ventro-apical
lobe produced caudad into a prominent lobe, the serrate margin directed
dorso-caudad; dorsal lobe broadly rounded and bearing along dorsal and
apical margin a series of prominent spines and protuberances each bearing
a short seta. Clasper short, apex upturned and sub-acute; baso-dorsal lobe
short and digitate, lateral lobe long, slender and acute; meso-apical surface
bearing a short slender acute process projecting just to apex. Aedeagus short,
arcuate, bearing no accessory structures.
Holotype male, Peavine Ridge, McMINNVILLE, OREGON, June
29, 1950, K. M. Fender.
Lepidostoma mira Denning, new species
This species belongs to the unicolor group with distinguishing
characters confined to the tenth tergite and the peculiar first
antennal segment.
Male.—Length 8 mm. Wings, legs and antennae light brown. Maxillary
palpi apparently one segmented, about two and one-half times length of head,
distal two-thirds covered with a dense brush of scales and setae. First anten-
nal segment about twice length of the head, mesal margin with a digitate
projection producing a distinct incision (fig. 3B); lateral and mesal margin
bearing a dense brush of dark brown setae. Basal portion of costal cell of
front wing folded over to form a small pocket densely lined with dark brown
scales, scattered brownish scales over remainder of wing.
Genitalia as in fig. 3. Dorsal lobes of tenth tergite, from dorsal aspect
(fig. 3C) emarginate; ventral lobe projecting caudad and sub-acute apically.
Tenth tergite from lateral aspect (fig. 3A) with a prominent quadrate spur
along lateral surface of dorsal lobe, consisting of a dorsad and caudad
directed apex; ventral lobe produced caudad beyond remainder, bearing a
large spur near base of lobe and a small spur toward apex. Claspers short,
constricted distally to a dorsad directed bifid apex; baso-dorsal lobe fairly
slender, lateral lobe closely appressed to dorsal margin of clasper, slender
and finger-like. Aedeagus bearing a pair of acuminate rods widely separated
and closely appressed to structure.
Female—Length 8 mm. Color, size and general structure same as for
male. First antennal segment long, about two and one-half times length of
head. Spermatheca as in fig. 3D.
190 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
Holotype male, STRAWBERRY, TUOLUMNE Counry, CALIFORNIA,
July 8, 1951, E. L. Silver. Allotype female, same data as for holo-
type. Paratype males, 1 male, same data as for holotype; 1 male,
Castle Lake, Siskiyou County, California, Harry Chandler. Holo-
type deposited in the collection of the University of California,
Berkeley, California.
Lepidostoma spicata Denning, new species
This species is a member of the unicolor group. It may be dis-
tinguished from other Lepidostoma by the tenth tergite and the
peculiar first and second segments of the antennae.
Male—Length 9 nm. General color of wings, legs, antennae and body
light brown. First antennal segment very large and bulbous, somewhat quad-
rate, posterio-mesal portion somewhat fiap-like with each segment approxi-
mate; second antennal segment (fig. 4C) with a flattened mesad directed
arcuate process, the inner surface of semi-circle thus formed densely lined
with short blackish setae. Maxillary palpi apparently one segmented, pro-
jected above head, apices flattened, mesal surface grooved and convergent,
lateral and ventral margins clothed with long brownish setae.
Genitalia as in fig. 4. From dorsal aspect, tenth tergite (fig. 4B) emarg-
inate, resultant dorsal lobes bearing several small spines distally; ventral
lobe occupies most of tergite and very spinous. Tenth tergite from lateral
aspect (fig. 4A) with dorso-distal corner of dorsal lobe bearing several small
spines; ventral lobe with ventro-distal corner broadly rounded and spinous.
From lateral view entire distal portion of tenth tergite appears covered with
spines of variable shapes and sizes. Claspers extend beyond tenth tergite
only a short distance, apex sub-truncate, baso-dorsal lobe short, digitate;
lateral lobe longer, slender and parallel to clasper. Aedeagus tubular, apex
sub-membraneous and bearing a pair of very large acuminate rods, shorter
than aedeagus; large size and shape unusual for this group.
Holotype male, Twin CREEK Camp, BirrERootT Mountains,
SALMON, IpaHo, 5000’ elevation, July 25, 1952, Borys Malkin.
Paratype male, same data as for holotype.
Lepidostoma astanea Denning, new species
This species is a member of the wnicolor group. Distinguishing
characters are present in the tenth tergite with its prominent dorsal
spine and elongated ventral lobe.
Male.—Length 7 mm. First antennal segment long and slender, other-
wise not modified. Maxillary palpi apparently two segmented, directed dor-
sad to near margin of head, mesal surface bearing a dense brush of blackish
scales and setae. About three-quarters of the costal cell of the front wing
EXPLANATION OF FIGURES
Fig. 1. Lepidostoma errigena, male genitalia; 1A, lateral aspect; 1B,
clasper, ventral aspect. Fig. 2. Lepidostoma recina, male genitalia; 2A, lateral
JULY, 1954] DENNING—LEPIDOSTOMA 191
RECINA
38
SPICATA
MIRA 30
3c
ASTANEA TIBIALIS
fr J
REQSA
8A STROPHIS
6A
aspect; 2B, tenth tergite,-dorsal aspect. Fig. 3. Lepidostoma mira, male and
female genitalia; 3A, lateral aspect; 3B, basal segment antenna; 3C, tenth
tergite dorsal aspect; 3D, spermatheca. Fig. 4. Lepidostoma spicata, male
genitalia; 4A, lateral aspect; 4B, tenth tergite, dorsal aspect; 4C, second
segment antenna. Fig. 5. Lepidostoma astanea, male genitalia; 5A, lateral
aspect. Fig. 6. Lepidostoma reosa, male genitalia; 6A, lateral aspect; 6B,
tenth tergite, dorsal aspect; 6C, clasper, ventral aspect. Fig. 7. Lepidostoma
tibialis, male genitalia; 7A, lateral aspect; 7B, tenth tergite, dorsal aspect.
Fig. 8. Lepidostoma strophis; basal segment antenna.
192 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXX, NO. 3
reflexed although resultant pocket is not wide, pocket filled with blackish
scales. Spurs 2—44, ;
Genitalia as in fig. 5. Ninth segment annular, where it merges into tenth
tergite there is a cluster of small spines. Tenth tergite from dorsal aspect
with short emargination. From lateral aspect tenth tergite (fig. 5A) with
apico-dorsal corner produced into an acute prominent dorsad directed spur,
at base of which there is a cluster of spines which are very prominent from
either dorsal or ventral view; ventral lobe produced caudad as a large ob-
tuse process. Clasper slender throughout, abruptly constricted distally into
a truncate apex; baso-dorsal lobe short, about one-third length of lateral
lobe which is slender, acute and reaches nearly to apex of clasper; short,
slender mesal process present near apex. Aedeagus with no accessory struc-
tures.
Holotype male, Patrick Creek, Det Norte County, CAtt-
FORNTA, June 24, 1951, D. G. Denning.
TOGATUM GROUP
Lepidostoma reosa Denning, new species
This species is a member of the togatwm group in which the
tenth tergite is produced caudad into a pair of lateral arms. In
this species, reosa, the claspers are not elongate as in togatum,
knowltont, tibialis and carolina, the only members of this group.
Another character which quickly separates reosa is the dorsad
curving rather than ventrad of the tenth tergite lateral arms.
Male.—Length 5 mm. General color brownish. Maxillary palpi apparently
one segmented and erect. Wings, legs and antennae with no particular
modifications.
Genitalia as in fig. 6. Tenth tergite, from lateral aspect, (fig. 6A) with
dorsal margin arcuate; ventral lobe extended caudad as a slender dorsad-
directed arm, apex obtuse and bearing two small spines. Tenth tergite, from
dorsal aspect (fig. 6B) separated on meson nearly half the distance, the
two lateral arms gradually convergent but not confluent; approximately
midway, lateral margin produced into an acute angulation. Claspers short
and robust, apex truncate; baso-dorsal process slender and directed dorso-
caudad; from ventral aspect (fig. 6C) no basal angulation, near apex a
short acute mesal process. Aedeagus with no accessory structures.
Holotype male, BELCHERTOWN, MassacuusettTs, May 21, 1938,
(from University of Massachusetts Collection).
LEPIDOSTOMA TIBIALIS (Carpenter )
1947 Lepidostoma rileyi Denning, Ent. News, LVIII, No. 10:257 figs.
9, 10 (New synonymy).
Distinguishing characters are in the tenth tergite; the dorsal
lobe is very short while the ventral lobe is produced caudad into
a heavily sclerotized acute process, as seen from either the lateral
aspect (fig. 7A) or dorsal aspect (fig. 7B). The species has been
recorded only from North Carolina, Georgia and Tennessee,
JULY, 1954] DENNING—-LEPIDOSTOMA 193
Several collections of Trichoptera have yielded some very in-
teresting distributional data of some species of Lepidostoma. They
are as follows:
Lepidostoma cascadensis Milne—This is a typically Western
species. The following records extend the known range northward,
Yukon Territory: Alaska Highway, Mile Post 632, June 28, 1952, C.
P. Alexander.
Alberta: Jasper, June 16, 1952, C. P. Alexander.
Lepidostoma cantha Ross.—Previously known only from Mon-
terey and Contra Costa Counties, California. The present record
extends the distribution to the southern part of the state.
California: Topanga Canyon, Los Angeles County, May 30, 1952, John
Belkin; Pinnacles National Monument, Monterey Co., May 3, 1946, H. P.
Chandler.
Lepidostoma frosti Milne-—Known distribution in the North-
east; New Hampshire, Massachusetts, Quebec and now Nova Scotia.
Nova Scotia: Cape Breton, Lake Bras D’or, July 4, 1951, C. P. Alexander.
Lepidostoma hoodi Ross.—Previously known only from Mt.
Hood, Oregon and Nanaimo, B. C.
‘Washington: Mt. Rainier, Aug. 4, 1952, Vincent Roth.
Lepidostoma ontario Ross.—Kastern in distribution: Ontario,
New Hampshire and Maine.
Nova Scotia; Cape Breton, Victoria Co., July 1, 1951, C. P. Alexander.
Lepidostoma podager (McL.).—Definite records have been
available only from California. The following record extends the
species into the Rocky Mountain area.
Wyoming: Madison Jct., Yellowstone Natl. Park, July 6, 1946, Marion
E. Smith.
Lepidostoma quercina Ross.—Until now recorded only from
Oregon and Idaho.
Washington: Kuschi Creek, near Goldendale, May 29, 1952, D. G.
Denning.
Lepidostoma querla Denning.—Previously record only from
type locality, Oak Creek Canyon, Arizona.
Arizona: Diamond Creek, White Mts., June 20, 1950, R. H. Beamer.
Lepidostoma roafi (Milne).—Well distributed in the western
half of the country. The following are new northern records.
Yukon Territory: Alaska Highway, Mile Post 632, June 28, 1952, C. P.
Alexander. Alberta: Banff, Aug. 14, 1949, C. P. Alexander.
Lepidostoma swannanoa Ross.—Kastern in distribution: New
Hampshire, New York, North Carolina and now Massachusetts.
Massachusetts: Amherst, June 9, 1941, Marion E. Smith.
Lepidostoma strophis Ross.—Transcontinental and well dis-
194, THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
tributed through the West, but unrecorded from Idaho. The first
antennal segment, with the peculiar knob along the mesal surface
near the base of the segment, is illustrated in fig. 8A.
Idaho: Lewiston, May 25, 1952, D. G. Denning.
Lepidostoma togatum (Hagen) —Distributed through the east-
ern half of the country. The Alberta record extends the known
range northwestward.
Alberta: Wahamum, July 13, 1939, E. H. Strickland. Nova Scotia: Hali-
fax Co., near Ecum Secum, June 29, 1951, C. P. Alexander; Inverness Co.,
Margaree River, July 3, 1951, C. P. Alexander.
Lepidostoma unicolor (Banks) —Widely distributed from Min-
nesota to the Pacific Coast and northward into Saskatchewan. Now
known to occur in the Southwest.
Arizona: Big Creek, Graham Mts., Graham County, Aug. 19, 1952, Hugh
Leech. California: Tanbark Flats, Los Angeles County, July 2, 10, 26, 1952,
A. T. McClay.
ANOTHER WEEVIL INJURIOUS TO STRAWBERRIES
On July 11 of 1953 the author was called to examine a field of
strawberries near Hillsboro, Oregon, that had been severely in-
jured by weevil larvae. The larvae had eaten into the crowns of
the plants and killed many of them. The injury was so severe that
the grower later plowed up the field. This weevil may become
quite injurious if it spreads to other strawberry growing districts.
Adult weevils were found feeding on the edges of the leaves and
resting under the foliage. They were identified by Miss Rose E.
Warner of the National Museum as Peritelinus oregonus Van Dyke.
In a personal letter, C. F. W. Muesbeck stated that P. oregonus
had been taken on filbert leaves in Oregon and on Achillea lanulosa.
This is the first time it has been recorded on strawberries.
The original description by Van Dyke’ states that the type
series was collected on oak, Quercus Garryana at Corvallis on June
3, 1914. He also mentioned specimens from Klamath Falls, Oregon,
collected on July 9, 1934. There are other Oregon records from
Salem, Dallas and Alsea Mountain. The seasonal dates of collection
of the adults range from April 27 to July 11.—R. G. RosEnstTIEL,
Oregon State College, Corvallis.
1 Van Dyke, Edwin C. 1936. New species of North American weevils in the
family Curculionidae, subfamily Brachyrhininae, V. Pan-Pacific Entomologist,
TOA )er 9-822
JULY, 1954] MOORE—ENDEODES 195
NOTES ON ENDEODES LECONTE WITH A DESCRIPTION
OF A NEW SPECIES FROM BAJA CALIFORNIA
(Coleoptera: Malachiidae)
Tan Moore
El Cajon, California
In this paper, a new species of Endeodes is described from
Baja, California, Mexico; one previously described species is
treated as a synonym, and some notes on habitat and extensions
of range are recorded.
The genus Endeodes is known only from the marine littoral
of the Pacific Coast of North America. Two of the species of the
genus (basalis and blaisdelli) are found abundantly only south of
Point Conception, California, and have several characteristics in
common which they do not share with the three more northern
species. The two southern species are found from May to Novem-
ber, almost exclusively under debris, largely dried seaweed, just
within the reach of the highest tides on the sandy beaches in
association with the much more abundant Phyconomus marinus
(LeConte) and Epantus obscurus (LeConte). In each of the
southern species the elytra are at least twice as long as wide, so
that they normally cover part of the abdomen. In the three more
northern species, the elytra are very much shorter, each elytron
being very little longer than wide, so that it does not extend over
the abdomen.
I have found two of the latter species (insularis and rugiceps)
in September and October, largely in association with Thallaso-
trechus in cracks in the rocks which were exposed at low tide.
Extensive collecting on the sandy beaches uncovered a few
specimens of collaris on one occasion under a sheet of galvanized
iron and, although Epantis obscurus (LeConte) and Phyconomus
marinus (LeConte) were both common in this area, I was unable to
find Endeodes associated with them. Blackwelder (1932) states
that his specimens were taken largely under driftwood.
Blackwelder’s excellent revision of the genus (Pan-Pac. Ent.,
VIII, p. 128, 1932) is sufficient for easy identification of the
previously known species, but a new key is presented here to in-
clude the new species which cannot be incorporated with his key.
196 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XxX, NO. 3
A Key TO THE SPECIES OF ENDEODES LECONTE
J. Each elytron at least twice as long as wide . ........ 2
Each elytron not much longer than wide . ..... .. . .:3
2. Elytra concolorous, ferruginous .. . ‘ . blaisdelli
Elytra of bicolorous, ferruginous basally and ihe: scale: Ss basaies
3. Legs, antennae, and mouthparts darker than thorax ..... . 4
Legs, antennae, and mouthparts pale . . ... =... . . Iinsularis
Hentlead Mnlackel vase. Ma dea estes. Ye a PR! oe Eee Cou mins
Headtreddishs 42 jag oak -s . rugiceps
The following notes ened some new smileoulttion aa extensions
of range for some of the species.
Endeodes blaisdelli Moore, new species
Color ferruginous; abdomen, eyes and tips of mandibles black. Head
about as long as broad, covered with a fine, pale, sparse pubescence. Eyes
with a few very short hairs between the facets. Labrum and clypeus slightly
paler than head. Pronotum a little broader than long, widest at about the
apical third, considerably narrowed at base, sides rather evenly arcuate,
pubescence as on head. Elytra concolorous, pale ferruginous throughout,
somewhat translucent, the dark color of the abdomen showing through the
posterior fourth. Each elytron about twice as long as wide, only slightly
expanded apically, conjointly nearly forming a square, sutural margins
meeting for their entire length, apical margins nearly straight and truncate
at right angles to the sutural margins with narrowly rounded internal angles
and broadly rounded external angles. Elytra clothed in a fine sparse
pubescence with a few scattered erect setae. Legs entirely ferruginous
except for the black comb of setae on the second segment of the front
tarsi in the male. Tibiae covered with short setae which are denser on
apical half of middle tibiae. Abdomen shining black, a little lighter beneath,
with a very fine, sparse pubescence which is a little longer below than above.
Length 4.5 mm.
Male with second tarsal segment of anterior tarsus expanded over third,
terminating in a comb of stout, dense, black setae.
Female with anterior tarsus simple.
Holotype (Calif. Acad. Sci.) male, from CoLontA GUERRERA
Baga Catrrornia, Mexico, August 19, 1950. Allotype (Calif. Acad.
Sci.) female, same data as holotype. Paratypes sixty-seven speci-
mens from Colonia Guerrera, Baja California, Mexico, August 19,
1950, and one specimen from the same locality, May 28, 1950.
Two paratypes have been deposited in each of the following col-
lections: U. S. National Museum, Washington, D. C.; Museum
of Comparative Zodlogy, Cambridge, Mass.; American Museum
of Natural History, New York City; Chicago Natural History
Museum; Canadian National Collection, Ottawa; British Museum,
London; Collection of Dr. R. E. Blackwelder, Washington, D. C.;
San Diego Natural History Museum, San Diego, Calif. Ten para-
JuLy, 1954] MOORE—ENDEODES 197
types are in the collection of the California Academy of Sciences,
San Francisco, and the remainder in my own collection.
The sixty-nine specimens collected on August 19, 1950, in-
cluding the holotype and allotype, were taken from one very
limited section of beach under small patches of dry seaweed,
mostly rockgrass mixed with some kelp. The beach here is backed
up by high sand dunes extending south from the mouth of the
Santo Domingo River and gradually diminishing in size to near
the salt marshes north of San Quintin Bay. In about the middle of
this area, where the beach was slightly arched to seaward, a very
high tide had cut away the sand, leaving a bank about a foot high
and a thousand yards long. All the specimens were found within
a belt about two feet wide to seaward of this undercut, and were
more or less regularly scattered along its entire length. The beach,
for its entire length, in a belt about twenty feet above and ten
feet below the populated strip, was covered with similar patches
of seaweed; however, not a single specimen was found elsewhere
after several hours of careful searching.
This species is most nearly related to basalis by the length of the
elytra, but can be distinguished from it at once by the concolorous
elytra. It also differs from that species in the shape of the elytra,
which are strongly truncate and more nearly rectangular. There
is almost no variation in color in my entire series, and very little
variation in the shape of the elytra and the shape of the pronotum.
This species is named for the late Dr. Frank E. Blaisdell, whose
unlimited generosity with his own time was so helpful to me and
to many others.
ENDEODES BASALIS (LeConte)
I am unable to draw a line of distinction between basalis and
abdominalis in regard to the color of the abdomen or the shape of
either the pronotum or the elytra, and | can find no other consistent
difference to separate them. In my series of 245 specimens, there
are twenty-two with the abdomen either entirely yellow or entirely
ferruginous, and forty-four with it entirely black. The remaining
181 specimens display every gradation of color between the two
extremes, Over 100 of these have the abdomen largely reddish with
several small to large patches of black; and a few specimens have
the abdomen largely black with indistinct orange patches. Some
specimens have light smoky or dark smoky abdomens. In a small
series of specimens collected at La Jolla, California, the abdomen
198 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXx, NO. 3
is a clear yellow rather than ferruginous; and the clypeus and
labrum are opaque cream color in contrast to the translucent
ferruginous color of these parts in specimens of a more reddish
cast. However, there are specimens which seem to be intermediate
between these and the rest of the series; and they appear to possess
no other consistent characters for their separation. Variations in
the shapes of the elytra and pronotum are just as great as those
of color, and show no correlation with each other or with the
variations of color of the abdomen. I can only assume that they
are color variations of a single species.
Previously known from San Luis Obispo County to San Diego
County, California. I have collected a large series of all color
varieties except pure yellow, from Halfway House, Descanso Bay,
Baja California, Mexico, in July and August; and four specimens
of both black and mixed colors from Sausal, Baja California,
Mexico, in July. A series of specimens showing the range of vari-
ation has been deposited in the entomological collections of the
California Academy of Sciences, San Francisco.
ENDEODES INSULARIS Blackwelder
Previously known from San Miguel Island and the adjacent
Prince Island, California. I collected three specimens at Gaviota
State Park, Santa Barbara County, California, in October. The
islands are almost due south and nearly opposite this part of the
mainland. My specimens were taken in company with Thallaso-
irechus nigripennis Van Dyke from cracks in a tilted sedimentary
sandstone formation which was exposed by the low tide. They were
found below the mean high water mark.
ENDEODES COLLARIS (LeConte)
Known from Vancouver Island, British Columbia, south to
Monterey County, California. I have taken it in October from
cracks in the rocks below mean high tide in association with
Thallasotrechus nigripennis Van Dyke and Liparocephalus at Moss
Beach, San Mateo County, California; and from beneath a sheet
of galvanized iron on the sandy beach above the high water mark
at Santa Cruz, California, in October.
I am indebted to Mr. Hugh B. Leech of the California Academy
of Sciences for the loan of specimens and for many other favors,
and to the late Dr. Edwin C. Van Dyke for many helpful sug-
gestions in both the laboratory and the field.
guLy, 1954] HURD—XYLOCOPA CALIFORNICA 199
A POLYTYPIC INTERPRETATION OF THE CALIFORNIA
CARPENTER BEE XYLOCOPA CALIFORNICA WITH THE
DESCRIPTION OF A NEW SUBSPECIES AND NOTES
ON A POSSIBLE POLYTOPIC FORM
(Hymenoptera: Apoidea)
Pau D. Hurp, Jr.
University of California, Berkeley
In the course of preparing a review of the Carpenter bees of
California’ a new subspecies of Xylocopa californica has been
recognized in the material originating from the mountainous
regions of cismontane southern California.
Cresson (1864) characterized as a new species Xylocopa cali-
fornica from Fort Crook, California, and Xylocopa arizonensis
from Arizona. Cockerell (1904) remarked that he could find no
valid structural characters separating these two forms and regarded
them as subspecies. X. californica arizonensis, according to Cock-
erell, occurred from Los Angeles, California, eastward to New
Mexico and southward to San José de Guaymas, Mexico; cali-
fornica proper was restricted to northern California.
Ackerman (1916:230) states in his revision of the Nearctic
species that californica and arizonensis are specifically distinct.
This author mentions that he noted a difference in the genitalia of
the two forms and further remarked that he found differences in
coloration and in the expression of pale pilosity on the abdomen.
He gives the geographic range of californica as California, Nevada,
Colorado and South Dakota and that of arizonensis as Arizona,
New Mexico, Lower California, Texas, and Mexico. In the recent
Synoptic Catalog of Hymenoptera of America north of Mexico
Michener (1951) has accorded californica and arizonensis sub-
specific status listing californica arizonensis from Texas, New Mex-
ico, Arizona, California, Mexico (deserts) and californica proper
from South Dakota, Colorado, Nevada, Arizona and California.
The present writer has made a critical morphological study of
this complex and has been unable to demonstrate any structural
character, apart from color and the amounts of pale pilosity, which
1 The Carpenter Bees of California, Bull. Calif. Insect Survey (in manuscript).
200 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
could be used to regard these forms as separate species. Moreover,
a geographical analysis of the distribution of these forms clearly
indicates they are geographic segregates (see map).
On the basis of coloration, Xylocopa californica contains three
readily recognizable subspecies, which geographically replace one
another. Each subspecies uses different softwoods in which to nest.
The subspecies californica proper nests in redwood and incense
cedar; diamesa nests principally in Yucca whipplei; and ari-
zonensis uses various desert agaves and yuccas. From the high
mountain localities in southern California (San Bernardino and
San Jacinto Mountains) several specimens are available which are
phenotypically very much like californica proper and suggest the
possibility of a high mountain population which is using the
isolated stands of incense cedar in which to nest. If this is the case
it is possible that these bees are either of polytopic origin, having
been derived from the yucca-using diamesa, or may be isolates of
californica proper which have remained associated with these now
isolated stands of incense cedar. It is significant, however, that the
available specimens from these high mountain southern California
localities are not phenotypically equivalent to the Sierran popula-
tions of californica proper. A critical field study of these isolates
is needed before an understanding of origin and relationships can
be achieved.
The three subspecies concerned may be separated by the follow-
ing key.
KEY TO THE SUBSPECIES OF XYLOCOPA CALIFORNICA Cresson
1. Miles soe. one Pee UE tee ie que ie TOs Pia ater hs 2
Henitale sts tics ae adhere Eh ee Ah Brie One ee Bie Bae aS | 4,
2(1) Abdomen predominantly blue in color; fourth metasomal tergum
without a medially interrupted fringe of whitish hairs -_................- 3
Abdomen predominantly green in color; fourth metasomal tergum
with a medially interrupted fringe of whitish hairs. North coast and
Sierra Nevada Mountains of California and southern Cascade Moun-
tains? Ole Ore cone... tote Oh ee Ee Par Se seat Pale californica
3(2) Wings heavily infuscated with black and strongly violaceous; abdo-
men dark blue. Deserts of California, Arizona, Nevada, New Mexico,
Utah, Texas and Mexico 20 ccccccccccccccscsssecseceeseeseeeesseeeeesoess arizonensis
Wings paler, not heavily infuscated with black, less strongly violace-
ous; abdomen blue, often blue with traces of green. Mountains of
cismontane southern California northward to Monterey County........
Se NAL eee Te eRe TERS RRM ec Aue ot Ea MC oe PD diamesa
JuLy, 1954]
4(1)
5(4)
HURD—xXYLOCOPA CALIFORNICA
Abdomen predominantly blue
Abdomen predominantly green. North coast and Sierra Nevada
Mountains of California and southern Cascade Mountains of Oregon
BDC Fg Sisal Ure nal gt De AUR a eee eal amar i AL Sag californica
Wings heavily infuscated with black and strongly violaceous; abdo-
men dark blue. Deserts of California, Arizona, Nevada, New Mexico,
Utah, Texas and Mexico
Wings paler, not heavily infuscated with black, less strongly violace-
ous; abdomen blue, often blue with traces of green. Mountains of -
arizonensis
cismontane southern California northward to Monterey County
diamesa
17
T
45
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Xylocopa californica Cresson
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DISTRIBUTION MAP
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SCALE
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Fig. 1. — Distribution of Xylocopa californica Cresson within California,
202 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
Xylocopa californica diamesa Hurd, new subspecies
Diagnostic characters. — Male. Head, body, and legs blue, sometimes
with green reflections. Wings infuscated with black, violaceous, but much
less intense than in arizonensis, but darker than in californica proper. Abdo-
men without a fringe of pale hairs on fourth metasomal tergum. Female.
Similar to male, but wings somewhat darker.
Holotype male, allotype female, and one paratype female from
_CrystaL LAKE, SAN GABRIEL Mountains, Los ANGELES CouNTY,
CatirorniA, July 9, 1952, collected by Joan Linsley. Additional
paratypes are from the type locality, on June 29, 1950 (W. C. Ben-
tinck, A. T. MacClay, J. W. MacSwain, M. J. Stebbins, and H. N.
Yokoyama), on July 9, 1952, (R. L. Anderson, R. M. Bohart, E.
M. Evans, A. Gregarick, H. L. Mathis, A. T. McClay, S. Miyagawa
and J. H. Nakata), and on July 7, 1934, (C. D. Michener). Other
paratypes are from Camp Baldy, San Gabriel Mountains, Los Ange-
les County, California, July 4, 1928, (F. B. Foley), on June 26,
1950, flowers Fremontia (P. D. Hurd, Jr.), on July 11, 1950, (H.
L. Hansen, P. D. Hurd, Jr., J. D. Paschke), and on July 7, 1952,
(A. R. Maggenti). One additional paratype is from Tanbark Flat,
San Dimas Experimental Forest, San Gabriel Mountains, Los Ange-
les County, California, July 3, 1950, (H. M. Graham). The holo-
type and allotype are on deposit in the California Academy of
Sciences.
As the name diamesa suggests this subspecies is intermediate
in its character between californica proper and arizonensis. Geo-
graphically it occupies an intervening area betwen the aforemen-
tioned subspecies.
LITERATURE CITED
ACKERMAN, ARTHUR
1916. The Carpenter-Bees of the United States of the genus Xylocopa.
Journ. New York Ent. Soc., 24:196—209.
CockKeERELL, T. D. A.
1904. The Bees of Southern California. V. Bull. So. Calif. Acad. Sci.,
3(6) :86-87.
Cresson, Ezra T.
1864. Descriptions of several new species of North American Apidae.
Ent. Soc. Phila., 3:40.
MicHENER, CHARLES D, [in Muesebeck, C. F. W., ez al.]
1951. Hymenoptera of American North of Mexico Synoptic Catalog.
U. S. Dept. Agr. Monograph 2:1246.
juLy, 1954] ROZEN—OREOPASITES LARVA 203
MORPHOLOGICAL DESCRIPTION OF THE LARVA OF
OREOPASITES VANDUZEEI COCKERELL
(Hymenoptera: Anthophoridae)
JEROME G. ROZEN, JR.*
University of California, Berkeley
This paper represents the first description of the larva of a
member of the Ammobatini, a tribe composed entirely of parasitic
bees. Oreopasites, the only New World genus belonging to this
tribe, is parasitic on the panurgine bees of the genus Nomadopsis
Ashmead.
The specimens upon which this paper is based were recovered
from the cells of Nomadopsis anthidius (Fowler), a large species,
which gathers pollen from various species of Trifolium. The iden-
tification of the parasitic bee larvae was made by inference from
the great number of large-sized Oreopasites vanduzeei Cockerell,
which were found at the nesting site of the host bee.
Three of the parasitic larvae were exhumed and preserved. One
is a large-sized, yellowish specimen, which, on the basis of the
author’s experience with other bee larvae, is obviously the hibernat-
ing form. One, slightly larger, is whitish and is the fully-grown
larva which has not yet defecated and assumed the hibernating ap-
pearance. In lieu of a more appropriate name for this form, it will
be called the “white larva” because of its color, although body
form is just as striking a difference between it and the hibernating
one. The third larva is the first instar. :
In the description of these three larvae, the morphological
terms and the study techniques which were employed by Michener
(1953) have been adopted for the most part.
Because Michener (ibid.) in his comprehensive study of bee
larvae was not fully able to discern between hibernating and pre-
hibernating larval forms, it is perhaps worth-while to describe and
to discuss the differences between them for this species. These dis-
similarities are apparently due to several reasons, one of the main
ones being the elimination of the fecal material by the larva as it
enters the hibernating stage. The material consists of the undigest-
able portion of all the pollen which the individual has consumed
during the larval stage. The defecation of such a large quantity
undoubtedly causes the very marked difference between the body
1 The author wishes to express his thanks to Dr. E. Gorton Linsley, who very
kindly read the manuscript.
204, THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
shape of the two larvae, and may account for the “white larva’s”
having a smooth integument while the hibernating form has a
finely wrinkled one. Other differences between these two are prob-
ably associated with physiological changes in the organism as it
enters diapause and prepares to withstand the adverse winter
weather conditions.
The following is a summarization of the differences between
these two larvae. In the “white larva” the head capsule is in general
less sclerotized, as is evidenced by its comparative lack of rigidity
and lighter coloration. The hibernating larva has several folds
(figs. 5 and 6) on the lateral portions of the labiomaxillary region,
which may be mistaken for a suture separating the two component.
mouthparts. Such folds are absent in the “white larva,” so that it
is assumed that these folds are superficial, being due to the reduc-
tion of the body content after defecation. As is stated above, the
body integument of the “white larva” is smooth, whereas that of
the hibernating form is finely wrinkled. In color the “white larva”
is translucent white and not opaque with a yellowish hue as is the
hibernating one. Intersegmental lines are very shallow in the
“white larva,” while they are deeply incised in the other. The
“white larva” is subcircular; the hibernating form, seen in cross-
section through the apices of the dorsolateral tubercles, is strongly
dorsoventrally compressed, so that the body at its largest diameter
is nearly twice as wide as high. The shape of the dorsolateral tuber-
cles differs between the two forms; this dissimilarity is discussed
in the description of the larva. The main differences between the
two larval forms are those listed above. In all other major respects
the larvae are identical and are described together below as the
mature larva.
DeEscrRIPTION OF Mature LARVA
Head: Capsule with integument very lightly sclerotized, bearing few
scattered setae. Anterior and posterior tentorial arms very short in both
hibernating and “white” larvae; remaining portion of tentorium absent.
Posterior tentorial pits situated slightly below hypostomal thickening. Poster-
ior thickening of head capsule, except near connection to hypostomal thick-
ening, very faint, so that boundary between head and body difficult to distin-
guish; near hypostomal suture posterior thickening pronounced, though some-
what less so than hypostomal thickening, and running in the same direction
as, and as a continuation of, hypostomal thickening. Hypostomal thickening
and corresponding suture pronounced. Pleurostomal thickening pronounced.
Epistomal thickening and corresponding suture between precoilae and an-
terior tentorial pits weak, though evident; epistomal thickening between
juLy, 1954] ROZEN—OREOPASITES LARVA 205
| MM.
.O5 MM.
PANTENNNS os oe Sole
4
~’ ANTERIOR
yas , TENTORIAL PIT ---_----
ae MANDIBLE - -~- --- ;
me Dyes
fa:
LABRAL TUBERCLE >
4
MAXILLARY PALPUS-/ |” Peel
HYPOSTOMAL SUTURE” BD
LABIAL PALPUS’
POSTERIOR TENTORIAL PIT“
POSTERIOR THICKENING OF HEAD CAPSULE.
PARIETAL BAND |
a
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PLEUROSTOMAL SUTURE.______---"K'/ Ni
_---LABRAL TUBERCLE- —_-_ -_ ----- fe
(PARRA De Fee a a0 Tie es
MANDIBLE — i
LABIAL PALPUS- - — _ — Beet ara ints
SALIVARY OPENING- - ---- bce es "
‘ ne -7 HYPOSTOMAL SUTURE !
hoe SP eater 2 MAXILLARY PALPUS —- —— - - “POSTERIOR TENTORIAL PIT
EXPLANATION OF FIGURES
OREOPASITES VANDUZEEI Cockerell
Fig. 1, hibernating larva, lateral view; fig. 2, spiracle; fig. 3, first instar,
dorsal view of head; fig. 4, first instar, lateral view of head; fig. 5, hibernat-
ing larva, front view of head; fig. 6, hibernating larva, lateral view of head.
206 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
anterior tentorial pits obscure, perhaps extending upward and running im-
mediately mesad of each antenna; epistomal suture absent. Antennae low
convexities. Parietal bands faint, clearly seen only on cleared head capsule.
Labrum protruding (in drawn specimen labrum has been somewhat flattened
and tubercles abnormally directed ventrad instead of anteriad as in “white
larva’) ; integument with minute spicule-like projections and apically with
scattered sensilla; labral tubercles long, attenuate. Hypopharynx united
with surrounding maxillae and labium so as to be difficult to definitely delin-
eate, except perhaps for shallow, unsclerotized groove in approximate posi-
tion of hypopharyngeal groove; integument without spicules or sensilla.
Salivary opening circular, not labiate, and situated somewhat below supposed
hypopharyngeal groove. Mandibles at base stout; at apex pointed, curved
inward, and with upper and lower margin coarsely serrate; mandibles
nearly identical to those of Nomada fowleri Cockerell as drawn by Michener
(1953:1069) except dentition on cusp lacking. Maxillae so fused with sur-
rounding mouthparts as to be impossible to delineate, though evident apically
as slight, palpus-bearing convexities, which are weakly sclerotized in over-
wintering larva, and which lie immediately below mandibles; palpi small
but distinct, each bearing two apical sensilla; each maxilla with single sensil-
lum laterad of palpus. Labium exceeded by hypopharynx, not divided into
prementum and postmentum; palpi completely lost except apparently for two
sensilla, each of which is in approximate position of palpus.
Body: Integument minutely spiculate. Intrasegmental lines absent. Dor-
solateral tubercles in ‘“‘white larva’? very low, scarcely noticeable toward
posterior end of abdomen; in hibernating larva apex of tubercles as high as
elevation of body at median line, so that body surface, between apices of
tubercles on same segment, straight. Spiracular atrium protruding above body
wall, with rim, and with rows of small teeth on inner surface; peritreme flat
or perhaps slightly concave.
It may be of some interest to note that of the three spiracles of
mature larvae to be examined, one, that of the hibernating larva,
contained in the atrium a single pollen grain of Trifolium and the
two from the “white larva” contained in their atria three and four
pollen grains. While the atrial opening is large enough to allow the
pollen grains to enter, the collar of the primary tracheal opening
is sufficiently small to exclude the grains from entering the sub-
atrium.
On the basis of the morphology of the mature larva, Oreopa-
sites seems to fall well within the Neopasites-Nomada-Epeolini
group, a group which, though appearing unrelated in adult charac-
teristics, has larvae which are very similar to one another as re-
ported by Michener (1953). The larva of Oreopasites shares with
this group the following characters which are listed by Michener
(1953:1066) for the group: salivary opening reduced, without
lips; antennal papillae reduced; mandibles acute at apices. Within
JULY, 1954] ROZEN—OREOPASITES LARVA 207
this group of parasitis bees, Oreopasites seems to be most similar
to Nomada as is shown by the following list of characters which
the two genera hold in common: head capsule weakly sclerotized,
broadly attached to body; posterior thickening of head capsule
weak; tentorial pits weak; mandibular shape and dentition (except
on cusp); labiomaxillary region reduced; spiracular shape; and
over-all body shape.
Oreopasites differs from the above mentioned group in the
peculiar position of the posterior tentorial pits; the unspiculate
hypopharynx; the lack of dentition on the mandibular cusp (also
lacking in the Epeolini), though the mandible is otherwise iden-
tical with that of Nomada; in the apparently even more reduced
labiomaxillary region, including the near loss of the labial palpi;
and from Nomada and Neopasites in the presence of atrial spines
which, moreover, are quite different from those of the Epeolini.
While the morphology of the mature larva of Oreopasites is
of particular interest because of the light it throws on the phylo-
genetic relationships of the genus (and the tribe) to other groups,
the morphology of the first instar is of interest because of the
adaptation of the first instar for killing the egg or perhaps young
larva of the host bee.
The first instar is markedly different from the mature larva.
Unfortunately, a complete description of the first instar is impos-
sible because of the specimen’s extremely small size (length 1.1
mm.) and because the specimen was about to molt, so that por-
tions of the integument of the second instar are visible and thus
obscure the structures on the first instar. However, a brief des-
cription is given and the head has been drawn (figs. 3 and 4), so
that at least some idea of the larva can be gained.
The head is elongate, more prognathus than that of the mature
larva. The labral tubercles are very long, extending anteriad well
beyond the closed mandibles. The mandibles are sickle-shaped and
beset with short teeth on their inner edge. The antennae, maxillary
palpi, and labial palpi have the same number of sensilla as the
mature larva. The posterior tentorial pits are in the same position
as in the mature larva. The post-cephalic region is slender, un-
curved, and not grub-shaped.
Mrcuener, C. D. LITERATURE CITED
1953. Comparative morphological and systematic studies of bee larvae
with a key to the families of hymenopterous larvae; Univ. Kansas
Sci. Bull., 35(8) :987-1102, 287 figs.
208 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 3
AN EFFICIENT METHOD OF COLLECTING DUNG BEETLES
In 1884, C. H. Roberts* recorded a method of collecting dung
beetles which, with some refinements, has proved so effective that
it seems worthy of recording again. The following implements are
used: A pail, a circle of 14-inch mesh wire screen of a small enough
diameter to fit into the pail, to the center of which has been secured
a weight (any small pipe fitting will do), a collecting jar of alcohol,
a strip of fine mesh wire window screen narrow enough to insert
into the collecting jar, and a five-gallon can of water. The dung is
placed in the bucket with the coarse mesh screen on top to hold
it down, and water added to cover. The beetles will some quickly
to the surface and may be easily scooped up with the strip of
window screen which is then dipped into the jar of alcohol to
dislodge them. In this way, the entire population of a single
dropping, sometimes hundreds of specimens, may be taken in a
very few minutes. This method is not only fast but relatively clean
if a spade is handy.—Ian Moore, El Cajon, California.
* ©. H. Roberts in “Miscellaneous Notes” Bull. Brook. Ent. Soc. 1884, VII, p. 74
BOOK NOTICE
THE COCONUT RHINOCEROS BEETLE (ORYCTES RHINOCEROS)
WITH PARTICULAR REFERENCE TO THE PALAU ISLANDS. By
J. Linsley Gressitt, Honolulu; Bernice P. Bishop Museum Bulletin 212
vili+157 pp., 50 figs. November 1, 1953.
The Palaus include 343 islands and islets, and form a group near the.
westward limits of the Caroline Islands, north of New Guinea. The destruc-
tive Oryctes rhinoceros (Linnaeus) is thought to have been introduced
into a central island, Koror, during 1942, by Japanese shipping. Because
of an abundance of war-killed palms, the beetles were able to spread and
within ten years kill 50% of the palms in the Palaus. O. rhinoceros was
introduced into the Samoan Islands over 40 years ago but has there killed
only about 12% of the palms. The adults prefer mature coconut palms
but will attack those of any age; they will feed on many other kinds of
palms, native and introduced, as well as on Pandanus, sugar cane and
pineapple. Larvae breed in dead trunks and stumps, compost piles, saw-
dust pits, and other places where there is sufficient humus. 4
Dr. Gressitt’s paper is based on six months of study in the Palaus and
one in the Samoan Islands, 1951 and 1952 (sponsored by the Pacific Science
Board), plus a review of the literature. Included are illustrated discussions
of the morphology, biology and ecology of O. rhinoceros in its various
stages, damage evaluation and population studies, and biological, cultural
and chemical control. There is a biblography (pp. 132-147) of 310 items,
and a full index. Most of the 50 figures are compound.—Hueu B. Leecu.
JULY, 1954) BAILEY—RHIPIDOTHRIPS 209
A REVIEW OF THE GENUS RHIPIDOTHRIPS UZEL
(Thysanoptera: Aeolothripidae)
STANLEY F. BAlLEY
University of California, Davis
This genus of thrips has been considered chiefly European.
Recent findings of two species in California (Bailey and Cott,
1952) and Oregon, however, have added it to our North American
fauna. Therefore, Rhipidothrips becomes a part of our series of
reviews of the thrysanopterous genera. Since it is such a small
group we have included all known species.
In addition to the species given in the key below, several other
thrips have been assigned to the genus Rhtpidothrips. The Aus-
tralian species aureus, described by Moulton, 1935, has been
studied and found to belong in a new, yet undescribed genus re-
lated to Desmothrips. R. turneri Moulton, 1930, was made the
type of the new genus, Rhipidothripiella, by Bagnall in 1932. In
turn, Bagnall‘s species uzelianus is now synonymized with gratiosus
Uzel.
Acknowledgments are very much in order as we are indebted
to H. Priesner and J. D. Hood for the loan of valuable specimens.
Without this considered cooperation such reviews in the Thysanop-
tera are nearly impossible. In addition, we wish to thank E. S. Ross
of the California Academy of Sciences for making the Moulton
collection available.
Genus RuipipoTHRipPs Uzel, 1895
Head longer than wide, slightly produced beyond eyes, broadly attached .
to thorax. Compound eyes prolonged ventrally. Ocelli present. Maxillary
palpi 3-segmented. Labial palpi 4-segmented. Antennae 9-segmented, the ter-
minal three segments fused, the third long; segments III and IV with ventral
clear lense-shaped sensory areas at distal position, sometimes nearly forming
a band around the segment. Pronotum wider than long with lateral suture at
each side along the long axis of the body. Bristles weak at anterior margin
usually with one longer than others at each posterior lateral angle and two or
more pairs along posterior margin. Fore tarsus with hook and a strong
spine at distal end of fore tibiae. Wings broad and rounded; fore wings
with typical aeolothripid veination with the exception of vestigial cross-
veins in the posterior portion; brachypterous forms with reduced veina-
tion (fig. 10). Abdomen broadly joined to thorax, tapering sharply at
posterior, ovipositor up-curved. Terminal segments of male without claspers,
heavy spines or chitinized projections (fig. 2).
Genotype: Rhipidothrips gratiosus Uzel, 1895. By monotypy.
See also Priesner, 1949, p. 147.
210 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
This genus belongs in the group aeolothripini and har the rare
venra Arhipidothrips Bagnall, 1932 (Faure, 1941) and Rhipido-
ihripiella Bagnall, 1932, as its relatives. Other members of this
group are Euceratothrips Hood, 1936, Lamprothrips Moulton,
1935, Pseudaeolothrips Bagnall, 1932, and the very large, world-
wide genus Aeolothrips. Aside from this last-mentioned genus,
extremely few specimens have ever been taken and, at present, it
is impossible to evaluate the group as a whole. We believe the mem-
bers of the genus to be predaceous (see also Bagnall and John,
1935), feeding on the larvae of other thrips as Anaphothrips,
Chirothrips, Limothrips, etc. Rhipidothrips appear to reach the
peak of seasonal abundance at the time the larvae of the above
mentioned genera are most numerous on grains and grasses.
KEY TO THE SPECIES OF RHIPIDOTHRIPS
1. Antennal segment II yellow; dorsum of head with a distinct collar of
polygonal reticulations at posterior (fig. 4) 2222. gratiosus
— Antennal segment II brown or grey; dorsum of head transversely striate..2
2. Forewing of macropterous forms with a brown cross-band; abdominal
segments IV and V white; antennal segment IV white ................ cinctus
— Forewing without cross-bands; abdominal segments otherwise colored
or uniform brown; antennal segment IV pale yellowish brown to dark
Je op AU eet Mee) is ZIRE 5 Merete atl oe eSB. Se 2 Een WA SL, 0 Cle Ra 2 3
3. Large species, body length 2.5 mm.; length of antennal segment III .087
mm., VIII .008 mm.; tip of antennal segment III dark brown ...-kellyanus
— Smaller species, body length about 1.6 mm.; antennal segment III, .064
mms be .013—020Rmnime: I yellow stu 28) 29 es be Se eee 4
4. Bristles behind eyes few, weak; intercollar bristles weak. Transverse
striations on dorsum of head uniform, one line heavier than remainder,
giving the appearance of a posterior collar (fig. 3)....W.........-..... nivelpennis
— Cluster of short stout bristles behind eyes, intercollar bristles strong;
striations on dorsum of head forming a collar-like appearance at pos-
terior (condition unknown in cahirensis); remainder of surface weakly
Stabe Ge Trey | graeme a 8 Me! Ae eo «ae te ee ea brunneus and cahirensis
DISCUSSION OF THE SPECIES
RHIPIDOTHRIPS BRUNNEUS Williams
1913. Williams, C. B. Jour. Econ. Biol. 8 (4); 216~218.
1926. Priesner, H. Thys. Eur. Wagner. Vienna. Page 97.
Female (brachypterous). Body dark brown with red subhypodermal
pigment which does not extend into the appendages. Distal portions of
tibiae and all of tarsi are yellow. 'Wing stubs (fig. 10) faint smoky grey.
Antennal segments are-colored as follows: I, dark brown; II, dark brown,
shading to yellowish brown at tip; III, yellow; IV, yellow, shading to
light brown at tip; V—IX, dark brown. Head with cheeks slightly arched
and a cluster of short spines on margin posterior to eyes, about as long as
wide (fig. 1). Three ocelli placed in a triangle, with one pair of moderately
JULY, 1954] BAILEY—RHIPIDOTHRIPS 2
long bristles placed just outside an imaginary line drawn from anterior
ocellus to each posterior one. Anterior ocellus minute. Surface of head
faintly cross-striate, heavier along posterior margin forming a collar. Maxil-
lary palpi three-segmented and labial palpi four-segmented. Mouthcone
short and blunt. Eyes normal and extending ventrally somewhat beyond
the dorsal posterior margin. Sensory areas on antennal segments III and IV
are on venter at distal end and are lense-shaped (fig. 5), that on segment
IV extending halfway around segment; two simple, slender cones on each
of segments V and VI, and one on VII. Pronotum slightly wider than long
and wider across anterior margin than posterior, with a lateral suture
extending two-thirds of its length on each side (fig. 1). One moderately
long bristle at each lateral posterior angle approximately at the, posterior
end of above-mentioned suture; one short bristle at each anterior-lateral
margin, directed forward, and two or three pairs along posterior margin.
A short irregular line or thickening occurs in the center and very faint
cross-striations are evident. Fore legs are short and heavy. The heavy
claw, typical of the family, is present on the fore tarsus and at the tip of
the tibiae are two heavy spines on the interior, one being more in the
nature of a spur. The ovipositor is up-curved and no other distinguishing
characteristics appear on the abdomen.
Female (macropterous). Our study is based on only one California
macropterous specimen. This form is slightly larger than the brachypterous
forms, and the setae are somewhat darker and longer. The short, thick bristles
behind the eyes and on the lateral margin of cheeks are present. The
reticulations on the head and pronotum and general coloration do not
vary significantly. For comparison with niveipennis particularly, we give the
measurements (mm.): head, length, 0.202, width, 0.190; interocellar bristles,
0.035—0.038; pronotum, length, 0.175. width, 0.297; bristles at posterior
lateral margins of pronotum, 0.044-0.048; forewing, length, 0.981, width
at center, 0.135; antennal segments, length I, 0.035; II, 0.051; III, 0.068;
IV, 0.064; V, 0.057; VI, 0.048; VII, 0.038; VIII 0.017; IX, 0.009. Total
body length, 2.05. Cross veins are absent in the posterior third of the
fore wing. The posterior third is colored a smoky brown, producing a faint
longitidunal band (fig. 12). Scalon (1931) first mentioned this form which
obviously is very rare.
This form is close to niveipennis as also pointed out by Speyer.
We have compared it with four specimens of the Reuter species
(det. by Priesner) and find that in the European specimens the
setae are weaker and colorless, the interocellars are 0.019—0.022
mm. long, the posterior lateral pronotals, 0.032—0.041 mm. and
the foréwing smaller, 0.864 mm. long, 0.094. mm. wide at center.
The cluster of short, stout bristles behind the eyes are entirely
absent or extremely weak.
Measurements (in millimeters) of brachypterous female: head, length,
0.192, width, 0.198; pronotum, length, 0.148, width (at anterior margin),
0.210; interocellar bristles 0.028, those at posterior lateral angle of pronotum
VA THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, NO. 3
.041—.043; total body length, 2.01. Anetnnal segments, length, I, 0.032; II,
0.048; IIT, 0.064; IV, 0.051; V, 0.051; VI, 0.041; VII, 0.032; VIII, 0.014;
IX, 0.011.
Male — unknown.
Material studied: Sussex, England, two females; Albany, Ore-
gon, three females; Granger, Oregon, five females; Corvallis,
Oregon, 14 females (Moulton, 1939) ; Vacaville, Fairfield, Skaggs
Island, and Palo Alto California, 43 brachypterous females, and
one macropterous female from Skaggs Island.
Hosts: Grasses, oats, Osmaronia.
Distribution: England, Siberia, Austria, France, North Amer-
ica: Oregon, California. The California records are new.
RHIPIDOTHRIPS CAHIRESIS Priesner
1932. Priesner, H. Bul. Soc. Roy. Ent. Egypt 25:45-46.
It has not been possible to study either of the two brachypterous
females on which this species was based. Comparing the description
with brunneus to which it is very closely related, we find the
principal difference to be that Priesner’s species is larger, and has
longer antennae. When a longer series is available from this part
of the world for comparison with brachypterous forms of brunneus,
it will be possible to more properly evaluate cahirensis. In the
meantime it must be keyed out with brunneus.
This species was based on specimens taken on “grasses on
March 27, 1930, near the Pyramids at a canal bank on the Sakkara
road, in Giza Province.”
RHIPIDOTHRIPS CINCTUS Hood
1918. Hood. Mem. Queensld. Mus. 6:121-122.
This species is known apparently only from the two original
females. It is readily distinguishable from all others described up
to the present time by the cross-band on the forewing and the
bicolorus abdomen. The important recognition characters appear
to be as follows: Antennal segments III and IV and abdominal
segments [V and V nearly white; pronotum smooth; maxillary
palpi three-segmented; macropterous, forewing with brown cross-
band in distal third, apex brown. The describer gave the length of
the nine antennal segments in microns as follows: 30, 48, 83, 72,
45, 31, 33, 20, 15; total 0.377 mm.
As far as we know the species has not been taken since its
original collection at Cooktown, North Queensland, February 4
and 24, 1912, sweeping, by A. A. Girault. Mr. George Mack,
JuLy, 1954] BAILEY—RHIPIDOTHRIPS 213
director of the Queensland Museum states that no types are on
deposit at that institution. We have not seen the species.
RHIPIDOTHRIPS GRATIOSUS Uzel
1895. Uzel, H. Monger. Ord. Thys. Koniggratz. Pages 66-68, figs. 42-43.
1926. Priesner, H. Thys. Eur. Wagner. Vienna. Page 96.
Female (macropterous). Body light brown, protonum yellow with an
irregular “x”-marking of brown in center, head dark brown. Tarsi all
yellow, distal and basal portion of tibiae yellow, as well as basal portion
of femora. Wings light grey with a smoky brown band longitudinally along
posterior fourth of forewing. Antennal segments colored as follows: I, dark
brown, II, yellow with dark brown ring at base, III, brownish yellow, dark
at tip, IV, smoky brown with dark ring at tip, V-IX, dark brown. Sensory
areas on segments III and IV extending two-thirds around segment (fig. 6).
Head longer than wide, cheeks slightly curved outwards with 3-4 moderately
heavy britsles at lateral margins behind eyes. Three ocelli present, normal,
with one pair of long seta (.038 mm. in length) on.a line with or within an
imaginary line drawn between the anterior ocellus and each posterior one.
Eyes normal, not. enlarged, but extending somewhat posteriorly beyond
the hind dorsal margin. Minor setae longer and more numerous on head
than on brunneus. Reticulations heavy and particularly prominent on poster-
ior portion of head thus forming a “collar.” Microtrichia present, directed
forward, on reticulations immediately anterior to collar. Maxillary palpi
three-segmented and labial palpi four-segmented (figs. 8, 9). Sensory areas
on antennal segments III and IV of the same type and similarly placed
as on brunneus but larger, in addition two or three faint circular areas
are present on the venter; those on the remaining segments are as in
brunneus. Pronotum wider than long. One small seta at each anterior lateral
angle and a scattered row of somewhat shorter setae along anterior margin.
One long seta (.064-.075 mm. in length) on lateral margin slightly forward
of posterior laterial angle and three or four pair of shorter bristles evenly
spaced, along posterior margin. The remainder of pronotum with scattered,
irregularly spaced, minor setae. Striations appear weakly at the center and
posterior margin. The lateral suture, so prominent in brunneus, is very faint
in gratiosus but the small mid-dorsal line is present. Fore legs normal with
a heavy tarsal hook on the underside, directed inward (fig. 11). Tibial
“spurs” as in brunneus but somewhat less strongly developed. Wings as in
brunneus (macropterous form) but slightly longer. Ovipositor normal.
Measurements (mm.) of female: head, length, 0.195, width, 0.174;
pronotum, length, 0.131, width, 0.198; forewing, length, 0.891, width (at
center), 0.135; total body length (distended), 1.94. Antennal segments,
length, I, 0.013; II, 0.210; III, 0.090; IV, 0.067; V, 0.054; VI, 0.044; VII,
0.035; VIII, 0.012; IX, 0.009.
Male. Bagnall (1913) and Morison (1948) record males from England.
Uzel, in his original description, stated that the male was smaller and more
slender than the female, similarly colored and the dorsum of the first
abdominal segment with the usual two ridges present. We have studied
seven males and note no claspers or thorns or dimorphism in the antenna.
214, THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
,
Lr pit POS
Fe Se
cand:
EXPLANATION OF FIGURES
Fig. 1. Head and pronotum of Rhipidothrips brunneus Wms. Fig. 2.
Terminal abdominal segments of Rhipidothrips gratiosus Uzel, male. Fig. 3.
Head and pronotum of Rhipidothrips niveipennis O. M. Reuter. Fig. 4. Head
and pronotum of Rhipidothrips gratiosus Uzel. Fig. 5. Antenna of Rhipido-
JuLy, 1954] BAILEY—RHIPIDOTHRIPS 215
To our knowledge there are no micropterous, brachypterous,
or apterous forms of this species.
Material studied: Cyprus, 1 female: Switzerland, 1 female;
France, 5 females, 5 males; Austria, 7 females, 2 males; North
America, California, 24 females.
thrips brunneus Wms. Fig. 6. Antenna of Rhipidothrips gratiosus Uzel. Fig.
7. Antenna of Rhipidothrips niveipennis O. M. Reuter. Fig. 8. Maxillary
palpus of Rhipidothrips gratiosus Uzel. Fig. 9. Labial palpus of Rhipido-
thrips gratiosus Uzel. Fig. 10. Fore wing pad of Rhipidothrips brunneus
Wms. Fig. 11. Fore tarsus and tip of tibia of Rhipidothrips gratiosus Uzel. Fig.
12. Fore wing of macropterous form of Rhipidothrips brunneus Wms. Scale:
figs. 1, 3, 4, 10, 12, line equals 0.1 mm.; figs. 2, 5, 6, 7, 8, 9, 11, line equals
0.01 mm.
216 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
Hosts: Barley, oats, wild grasses, “flowering Dicotyledons’’,
Coronilla varia.
Distribution: England, France, Bohemia, Hungary, Austria,
Switzerland, Cyprus.
New records: North America; California, near Beaumont, June
6, 1949, R. M. Bohart; San Luis Obispo, Pismo Beach, and Zaca
Mt., April 24, 1951, S. F. Bailey and R. M. Bohart. These are the
first records of the species in North America.
RHIPIDOTHRIPS KELLYANAS Bagnall
1924b. Bagnall, R. S. Ann. Mag. Nat. Hist., ser. 9, 13:584-585.
Bagnall based this Australian species on two females, which
from the description, is distinctly different from cinctus. The
coloration of the forewings is typical of European species and the
reticulated collar and the mottling on the head remind one of
gratiosus. The peculiar shortening of the eighth antennal segment
is a unique character but since this measurement is based on only
one perfect specimen, it is impossible to say whether or not this
is reliable. The writer recalls discussing this trips with the late
Dudley Moulton and he was of the opinion it did not belong in
Rhipidothrips. Nothing further can be done with this species at
present.
The two females were collected on April 22, 1923, on Eucalyptus
leucoxylon by R. Kelly, Mount Lofty Ranges, South Australia.
Supposedly the slide is in the Bagnall collection in the British
Museum, London, England.
RHIPIDOTHRIPS NIVEIPENNIS O. M. Reuter
1899. Reuter, O. M. Act. Soc. Faun. Flor. Fenn. 17(2) :30-31.
1926. Priesner, H. Thys. Eur. Wagner. Vienna. Pages 96-97.
Female (macropterous). Body dark brown with red subhypodermal
pigment. Distal portions of tibiae and all tarsi yellowish white. Wings
normal, nearly colorless, faintly yellowish brown near base of forewings
and along costal vein. Antennal segments colored as follows: I and II dark
brown, III and IV yellow, V brownish yellow, VI-IX brown. Head with cheeks
nearly straight with very weak spines, slightly longer than wide (fig. 3).
Three ocelli, anterior one smaller than laterals; surface completely cross-
striate, the lines anastomosing. Compound eyes prolonged ventrally; inter-
ocellar bristles short. Maxillary palpi three-segmented; labial palpi four-
segmented. Mouthcone extending slightly beyond the center of the prothorax.
Sensory areas on antenna ventral, oval, that on IV larger than on IU,
placed near tip; two small simple cones on each of segments V—VII (fig. 7).
Pronotum slightly wider than long; lateral suture present; surface
lightly cross-striate; one moderately heavy bristle at posterior lateral angles.
One pair on posterior margin at each side of center, one short seta at each
JuLy, 1954] BAILEY—RHIPIDOTHRIPS 217
anterior lateral angle, directed forward. Fore legs normal, with claw on
basal tarsal segment and a spur at tip of tibia. Abdomen typically aeolothrip-
oid in shape, ovipositor up-curved.
Measurements (in millimeters) ; head, length, .041, width, 0.38; prono-
tum, length .160, width, .166; total body length, 1.33. Antennal segments
(length) : 1,.028; II, .041; III, .072; IV, .057; V, .054; VI, .040; VII, .030;
VII, .013; IX, .008.
Male: not available for study; very rare.
Material studied: Three females (loaned from Hood collection)
det. H. Priesner, coll. Ahlberg. Sweden, Experiment alfaltet, May
30, 1919. Host unknown (probably grasses). One female col-
lected by Hukkinen, det. zy Priesner with no locality data.
Hosts: Grasses, Abies, Rubus, Galium, Solidago, Convallaria,
Taraxacum, Anthriscus, Urtica, Hieracium, and Alopecurus.
Distribution: Sweden, Finland.
Hukkinen (1935, 1942) reports both macropterous and brach-
ypterous forms from Finland. Speyer and Parr (1951) report
studying one of Hukkinen’s specimens which lacks the posterior
lateral bristles on the pronotum, thus agreeing with the original
description. The specimens we have studied all have setae on the
pronotum as shown in fig. 3. Neither of the above authors (or
Williams, 1916) mention other important diagnostic characters
such as post-ocular and interocellar setae as well as the nature
and extent of the dorsal reticulations on head and pronotum.
Speyer points out that Reuter may have had two species before him,
one of which is what we now believe to be the macropterous form
of brunneus. However, we note differences in the two forms of
brunneus and also point out that the brachyterous form (Hukkinen,
1935, 1942) of nivetpennis has not been fully described.
Some years thrips are known to produce many winged forms
and the following season they will be scarce. Not until a large
series of the two forms of these two species are collected and
studied can this matter be definitely settled. When only a few speci-
mens are available, it is possible that the individuals studied by
both Reuter and Speyer are atypical.
RHIPIDOTHRIPS UZELIANUS Bagnall
1934. Bagnall, R. S. Ann. Mag. Nat. Hist., ser. 10, 14:482.
This enigmatic species from Switzerland has not been clearly
defined and has to our knowledge not been taken since Bagnall
described it. The author distinguished it from gratiosus solely on
minor differences in the size of the wings ,head, tibiae, and shorter
218 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
intermediate antennal segments. We have not seen this species
but consider it of very doubtful validity. The only significant
difference in the measurements given by Bagnall is in the length
of antennal segment IV; that of gratiosus being given as 80 microns
and that of uzelianus as 59. In a series of 25 female gratiosus which
we have studied the length of this segment varies from 57 to 80,
averaging 71.5 microns. |
Morison (1948) lists this species from England, quoting Bag-
nall, but apparently did not collect it himself or critically study
Bagnall’s material.
In our collection we have one female of gratiosus taken and
determined by Bagnall at Zurich, Switzerland, with the same col-
lection data as the unique specimen of uzelianus with the exception
of the host being “oats” instead of “Brachypodium”. It is a typical
specimen of gratiosus with antennal segments of the following
lengths: 28, 48, 99, 80, 57, 48, 35, 16, 11. Nothing further can be
done to more definitely place this species until the type is studied
and more material collected.*
AHLBERG, OLOF REFERENCES
1920. Zur Kenntnis der schwedischen Thysanoptera. Arkiv. of Zool. Bd.
35 Nos 7, pp.2-3.6 9
1926. Tripsar. Thysanoptera. Svensk Insektfauna. Entom. for Stock-
holm. 6, 20-21, fig. 9, B.
Bacnat., R. S.
1909. A contribution to our knowledge of the British Thysanoptera
(Terebrantia), with notes on injurious species. Jour. Econ. Biol.
4(2) :41.
1912. A further contribution towards a knowledge of the British Thysan-
optera (Terebrantia). ibid. 7(4) :190.
1913. Further notes on new and rare British Thysanoptera (Terebran-
tia) with descriptions of new species. Jour. Econ. Biol. 8(4) :232.
1924a. Some new or little-known British Thysanoptera. Ent. Mo. Mag.,
ser. 3, 60:114. May.
1924b. On a new species of Rhipidothrips (R. kellyanus, sp. n.) from
Australia. Ann. Mag. Nat. Hist., ser. 9, 13:584-585. June.
1930. On some new and rare British thrips. Ent. Mo. Mag. 66:47.
1932. Description of some new genera and species of African Aeolo-
thripoid Thysanoptera. Ann. Mag. Nat. Hist. 10(57) :291-292.
1934. Contributions towards a knowledge of the European Thysanoptera.
V. Ann. Mag. Nat. Hist., ser. 10, 14:482.
* Since this paper was prepared, E. R. Speyer has called my attention to his
report of 1951 (Speyer and Parr, 1951) in which he has studied the type and al-
ready synonymized it with gratiosus.
JuLY, 1954] BAILEY—RHIPIDOTHRIPS 219
Bacnatt, R. S. and Oscar Joun
1935. On some Thysanoptera collected in France. Ann. Soc. Ent. France
104:311.
BaIruey, S. F. and H. Eowin Cort
Thrips new to California. State of Calif., Dept of Agric. Bull. 41(3) :177.
Faure, J. C.
1941. Records and descriptions of South African Thysanoptera. II.
Jour. Econ. Soc. So. Afr. 4:100-107, figs. 1-6.
Hoop, J. D.
1918. New genera and species of Australian Thysanoptera. Mem.
Queensld. Mus. 6:121-122.,
HuKKINEN, Y.
1935. Verzeichnis der Thysanopteren Finnlands. Ann. Ent. Fenn. 1
(3) :86, 88.
1942. Blick auf die Erforschung der Thysanopterenfauna Finnlands,
besonders ihrer schadlichen Arten. Ann, Ent. Fenn. 8(1) :28, 34, 35.
Ketiy, R. and R. J. B. Mayne
1934. The Australian thrips. Australian Med. Pub. Co. Ltd., Sydney.
Pages 13-14.
Morison, G. D. ;
1948. Tysanoptera of the London area. Part II. London Nat. Supple-
ment (Reprint No. 59). Page 38.
Mou tton, D.
1930. Thysanoptera from Africa. Ann. Mag. Nat. Hist., ser. 10, 5:197-198.
1935. New species of thrips from southwestern Australia. Jour. Roy.
Soc. W. Australia. 21:98.
1939. Rhipidothrips brunneus Williams. Pan Pac. Ent. 15(1) :20.
PriesNner, H.
1926. Thysanopteren Europas. Lief. I, Pages 95-97. Wagner, Wien.
1928. Verzeichnis der Thysanopteren Ungarns. Ann. Mus. National
Hung. 25:61.
1930. Die Thysanopteren-Typen O. M. Reuter. Deutsche ent. Zeitschr.
Heft. 1, P. 39. Berlin.
1932. Contributions towards a knowledge of the Thysanoptera of Egypt.
VIL. Bul. Soc. Roy. Ent. Egypt. 25:45-46.
1949. Genera Thysanopterorum. Bul. Soc. Fouad Ist. 33:38, 147.
Reuter, O. M.
1899. Forkecking och Beskrifnig ofver Finsaka Thysanoptera. Act.
Soc. Faun. Fenn. 17(2) :30-31, fig. P. 30.
SCALON, OLGA
1931. Thysanoptera nouveaux pour la Siberie. Konowia 10(2) :90.
Speyer, FE. R. and W. J. Parr
1950. Studies upon Thysanoptera. Exp. and Res. Sta., Cheshunt, Herts,
England. Pages 35-37, Plate 1, figs. 1-2. (Printed 1951.)
TREHERNE, R. T.
1921. Notes on the Aeolothripidae (2). Proc. Ent. Soc. B. C. No. 16,
System, Ser., page 11.
220 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXX, NO. 3
Uze., Heinricu
1895. Monographie der Ordnung Thysanoptera. Pages 66-68, Taf. V.,
figs. 42-43. Koniggratz.
Witiiams, C. B.
1913. Records and descriptions of British Thysanoptera. Jour. Econ.
Biol. 8(4) :216—218.
Wiiuiams, C. B.
1916. Biological and systematic notes on British Thysanoptera. The
Ent. 49:221-222.
USE OF BIRD NEST BY BUMBLEBEE
A nest of a bumblebee, Bombus caliginosus (Frison), was
found on May 1, 1954, in Berkeley, California in an old nest made
by house finches [Carpodacus mexicanus (Miller) ] in 1953 or
possibly 1952. The nest was placed about 15 feet above the ground
against the redwood siding of a house and was supported by twigs
of a broad-leaved ornamental shrub on the northeast side of the
house. When found, the bird nest was occupied by a queen bee
and contained a number of recently formed brood cells and a
pollen mass within which were present six larvae, three pupae, and
two egg masses of 9 and 10 eggs, respectively. Also present
was a small lepidopterous larva Hofmannophila pseudospretella
(Staint.)*. A new brood cell contained mites of the family
Laelaptidae’ of the genus Hypoaspis (s.l.).
The nest chamber of the bee was within the soft, collapsed mass
of bird nest material which was originally the lining. This con-
sisted of thin fibers, chiefly grass, and many small wads of cottony
and downy material apparently collected from plants such as
willows and from Eucalyptus flower-heads. The entrance to the
bee’s nest chamber was on top of the bird nest and led to a main
chamber an inch from the surface occupied by ihe pollen mass.
The new cell was inserted into another part of the nest and was
connected with the main passage in front of the pollen mass. The
bird nest was protected from rain by both the supporting shrub
and a roof overhang.
The over-winter use of a bird nest by Bombus is apparently
unrecorded, hence this note——FRANK A. PITELKA, Museum of
Vertebrate Zoology, University of California, Berkeley.
1Tdentified by H. W. Capps
2 Identified by D. P. Furman
JuLY, 1954] CAUSEY——-MILLIPEDS 221
NEW RECORDS AND SPECIES OF MILLIPEDS FROM THE
WESTERN UNITED STATES AND CANADA
NeELL B. Causey
Fayetteville, Arkansas
Dr. and Mrs. Herbert W. Levi and Mr. Joe Gorman collected the
millipeds reported here and kindly made them available to me.
Both collections are important because they contain several species
previously known only from the type collections. Holotypes will
be deposited in the American Museum of Natural History and
paratypes will be retained in the author’s collection.
ORDER COLOBOGNATHA
FamiLy ANDROGNATHIDAE
BRACHYCYBE PRODUCTA Loomis
Brachycybe producta Loomis, 1936. Proc. U. S. Nat. Museum, 83:367-368,
fig. 32, h, i.
One female of 53 segments, width 3 mm., was collected by Mr.
Gorman in Marin County, California, April 2, 1952.
ISCHNOCYBE PLICATA Cook and Loomis
Ischnocybe plicata Cook and Loomis, 1928. Proc. U. S. Nat. Museum, 72:
22-24, pl. 1, fig. 6.
One female of 57 segments was collected by Mr. Gorman at
Genosee, Plumas County, California, April 13, 1952.
EUCYBE CLARUS Chamberlin
Eucybe clarus Chamberlin, 1941. Bull. Univ. Utah, Biol. Ser., 6(4) :3.
One female of 58 segments, length about 20 mm., width 1.4
mm., agrees with the description of the female holotype except that
there are three transverse rows of tubercles on the collum. Collected
by the Levis at Patrick Creek, Del Norte County, Eee July
a oaees ORDER POLYDESMOIDEA
FAMILY XYSTODESMIDAE
HARPAPHE HAYDENIANA (Wood)
Polydesmus (Leptodesmus) haydenianus Wood, 1864. Proc. Acad. Nat. Sci.
Philadelphia (1864) :10; 1865, Trans. American Plilos. Soc. 18:226-227,
fig. 57,
Leptodesmus haydenianus (Wood), Bollman, 1893. Bull. 46, U. S. Nat.
Museum, 122.
Harpaphe haydeniana (Wood), Cook, 1904. Harriman Alaska ern 8(1):
59-60, pl. 3, figs 4a, 4b, 4c.
A few adults and numerous larvae of stadium VII were collected
by the Levis from moss and wet leaves along the shores of bodies
of fresh water at Cape Perpetua, Lincoln County, Oregon, July
8, 1951.
222 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXX, NO. 3
HARPAPHE POTTERA Chamberlin
Harpaphe pottera Chamberlin, 1949. Proc. Biol. Soc. Washington, 63:129,
fig. 10.
Several adult specimens were collected by Mr. Gorman at Low
Pass Creek, March 25, 1951; on Brock Mt., April 16, 1952; and
at Madison Creek, September 2, 1951, all in Shasta County, Cali-
fornia. Prefemurs of legs with shorter spines than in H. haydeniana.
HYBAPHE TERSA Cook
(Figure 1)
Hybaphe tersa Cook, 1904. Harriman Alaska Exped. 8(1) :58-59, pl. 3, fig. 3a.
Mr. Gorman collected specimens of both sexes April 16, 1932,
at Low Pass Creek and on Brock Mt., both in Shasta County, Cali-
fornia. The color is striking, with the prozonites green and the
metazonites red-orange. The femoral branch of the male gonopods
is flattened and easily bent. In each specimen the apex of the
femoral branch is slightly different, varying from acute, as il-
lustrated by Cook, to rounded (fig. 1) in some and finely bifid in
two. Another interesting variation is seen in the keels of segments
2 through 4; in some specimens there is a small but distinct tooth
on the anterior angle of each of these keels, while in others there
is only a trace of the tooth on one or more of these keels. Keels
of the collum sometimes have a similar small tooth. Dorsum mod-
erately arched, with low-placed keels on all segments except the last.
Keels of collum obtuse, lightly rounded; keels of segments 2
through 4 directed slightly cephalad, the caudal margins convex;
keels of segments 5 through 16 rectangular, the caudal margins
almost straight; keels of segments 17 through 19 increasingly re-
duced at the cephalic angles and produced at the caudal angle, with
the eighteenth slightly acute and the nineteenth more acute and
about half as large as the eighteenth. Prozonites of middle body
segments much exposed. Caudal spine narrow, truncated. Legs from
middle of body back with short, stout spine on the second article.
Tubaphe Causey, new genus
Telopodite of gonopods two-pronged, with both prongs simple
as in Hybaphe Cook, 1904 and Jsaphe Cook, 1904. Distinguished
from both genera by the absence of keels on segments 6, 8, 11, and
14 and by the presence of only rudimentary keels on the poriferous
segments. Coxae and prefemurs of legs spined, while in Hybaphe
only the prefemurs are spined; leg spination unknown in /saphe.
Genotype. Tubaphe levii Causey, new species.
JULY, 1954] CAUSEY—MILLIPEDS ‘993
Tubaphe levii Causey, new species
(Figures 2-4)
Male holotype. Colors faded, but the keels and perhaps the legs are red
and the dorsum is brown. With the middle and posterior keels either absent
or greatly reduced, the appearance is almost juloid. Keels of segments 1
through 4 are moderately large, obliquely depressed, with the angles rounded
and the lateral margins welted. Beginning abruptly with the fifth segment
and continuing on all of the poriferous segments, the keels are scarcely more
than longitidunal welts through which the pores open laterad; there is but
a slight trace of a welt on the nonporiferous segments (Fig. 2). Keels of
segments 14 through 18 are slightly larger and produced caudad; on segment
19, of which very little is exposed, the keels are much reduced; apex of
caudal spine narrow, truncated (Fig 3). Intrasegmental sutures distinct and
lightly corrugated; tergites smooth otherwise. Prozonites of middle body
segments much exposed. Sternites smooth and glabrous. Coxae of last legs
‘ well separated. Prefemurs of legs from middle of body back with stout, sharp
spines and coxae with stout, blunt spines.
Telepodites of gonopods subparallel and contiguous at the femoral region,
with the apices of the tibio-tarsi reaching in front of the sixth coxae. In
lateral view each of the two. prongs appears to form a semicircle; the curva-
ture as seen in medio-cephalic view is shown in Figure 4; the curvature is
altered by drying. Coxal region elongated, with the usual medial coxal hook;
femoral region elongated and separated from the tibio-tarsus by an oblique
suture. The long, attenuated femoral process arises from the medial surface
and curves dorso-cephalad. Width 4 mm.
Female paratype. Somatic characters agree with those of the male except
that the width is 5 mm. and the length is 33 mm.
Holotype, male: Graves CREEK Camp Grounp, Otympic Na-
TIONAL ForEST, JEFFERSON County, WASHINGTON; rain forest.
The Levis collected 1 male and 2 females July 12, 1951.
FAMILY NEARCTODESMIDAE
NEARCTODESMUS OLYMPUS Causey
Nearctodesmus olympus Causey, (in press). Ann Ent. Soc. America.
Several adults and larvae of stadium VII were collected by the
Levis at Cape Perpetua, Lincoln County, Oregon, July 8, 1951. The
apex of the lateral prefemoral branch of the gonopod bears three
minute prongs instead of the four in the holotype from Callam
County, Washington.
FAMILY POLYDESMIDAE
SCYTONOTUS AMANDUS (Chamberlin )
Polydesmus amandus Chamberlin, 1910. Ann. Ent. Soc. America, 3(4):
249-250; pl. 38, fig. 6; pl. 39, fig. 1.
Several adults and larvae of stadium VI were collected by the
Levis from the Gros Verte area, Moose, Teton County, Wyoming,
July 26, 1950.
224, THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 3
Brachydesmus (Brachydesmus) yosemitensis Causey, new species
(Figure 5)
Distinguished from B. hastingus Chamberlin, 1941, the most
closely related North American species, by the larger size and
details of the gonopods. Gonopods especially distinctive in the
irregularly serrated margin of the femoral lobe and the hooked
lobe near the hair pad.
Male holotype. Color red-brown. Caudal margin of metatergites straight
or slightly curved, with the caudal row of setae prejecting beyond the margin.
keels finely dentate laterad, sometimes obscurely so, with five uneven serra-
tions on the poriferous segments and four on the nonporiferous. Pores open
laterad on longitudinal tubercles. Metazonites with three rows of low, setifer-
ous, often indistinct tubercules, with 12 setae in each row. Transverse
depressions between rows of tubercles are more distinct than the longitudinal
depressions. Tubercles on keels tend to be indistinct. On most segments there
are eight large tubercles in the anterior row, eight smaller ones in the middle
row, and 12 little ones in the marginal row. Tubercles on eighteenth seg-
ment indistinct. Exposed parts of prozonites smooth; a raised transverse band
separates the pro- and metazonites. Anal valves and venter with abundant
short setae. Legs of segments 6, 7, and 10 unmodified, the other legs lost.
Gonopods as shown in figure 5. Width 1.3 mm., estimated length 11 mm.
Holotype male: VERNAL Fautus, Yosemite NATIONAL Park,
CALIFORNIA. One male with the head, first five segments, and most
of the legs lost was collected by Mr. Gorman February 2, 1952.
ORDER SPIROBOLOIDEA
FAMILY SPIROBOLIDAE
CALIFORNIBOLIS PONTIS Chamberlin
Californibolus pontis Chamberlin, 1949. Jour. Washington Acad. Sci., 39(5):
166, figs. 18, 19.
One male of 52 segments, width 5.2 mm., was collected by Mr.
Gorman at Low Pass Creek, Shasta County, California, April 16,
1952.
CALIFORNIBOLIS UNCIGERUS (Wood)
Spirobolus uncigerus Wood, 1864. Proc. Acad. Nat. Sci. Philadelphia, (1864) :
15; 1865, Trans. American Philos. Soc., 13:209-210, fig. 36.
Tylobolus uncigerus (Wood). Cook, 1904. Harriman Alaska Exped. 8(1) :67.
Californibolus uncigerus (Wood). Chamberlin, 1949. Jour. Washington Acad.
Sci. 39(5) :166.
EXPLANATION OF FIGURES
Hybaphe tersa Cook. Figure 1. Right gonopod, cephalic view.
Tubaphe levii Causey, new genus, new species. Figure 2. Segments 10
juLy, 1954] CAUSEY—MILLIPEDS 225
and 11, dorsal view. Figure 3. Segments 18-20, dorsal view. Figure 4. Left
gonopod, medio-cephalic view.
Brachydesmus (B.) yosemitensis, Causey, new species. Figure 5. Left
‘gonopod, lateral view.
f, femur; h, hair pad; 1, femoral lobe; s, seminal canal; t, tibio-tarsus.
226 THE PAN-PACIFIC ENTOMOLOGIST [VOL. Xxx, NO. 3
One male of 52 segments, width 6.4 mm., was collected by Mr.
Gorman at Low Pass Creek, Shasta County, California, April 16,
1952.
AxoBoLUs ERGUS Chamberlin
Axobolus ergus Chamberlin, 1949. Jour Washington Acad. Sci., 39(5) :163,
figs. 5-7.
One male of 52 segments, width 6.3 mm., was collected by Mr.
Gorman at Rich Bar, Plumas County, California, April 14, 1952.
ORDER JULOIDEA
FAMILY PARAIULIDAE
ORIULUS MEDIANUS Chamberlin
Oriulus medianus Chamberlin, 1940. Bull. Univ. Utah, Biol. Ser., 5(7) :7-8,
pl. 3, figs, 21, 22.
Several collections of adult specimens were taken by the Levis
in Teton County, Wyoming, and Fremont County, Idaho, in June,
July, and August, 1950. Only larvae were taken in Custer State
Park, South Dakota, June 25, 1950.
TAIULUS TIGANUS (Chamberlin)
Paraiulus tiganus Chamberlin, 1910. Ann. Ent. Soc. America, 3(4) :254-256,
SLO, Hee. pled fee, 128.
Taiulus tiganus (Chamberlin). Chamberlin, 1940. Bull. Univ. Utah, 30(11) :18.
Several adult specimens were collected by the Levis at Pines
Camp Ground, Mt. Nebo, Juab County, Utah, August 25, 1951.
TAIULUS sp.
Numerous larvae were collected by the Levis from fern fronds
in a rain forest at Cape Perpetua, Lincoln County, Oregon, July
8, 1951. Mr. Gorman collected larvae at Burney Falls, April 15,
and mature females and larvae at Madison Creek, Shasta County,
California, September 2, 1951.
FamMILy BLANIULIDAE
UroruLus utus (Chamberlin)
Nemasoma uta Chamberlin, 1912. Ann Ent. Soc. America, 5(2) :162-163.
Utotulus utus (Chamberlin). Chamberlin, 1943. Proc. Biol. Soc. Washington,
56:145.
Namasoma uta (Chamberlin). Chamberlin, 1951. Nat. Hist. Miscellany, No. 87,
p. 9, fig 21.
Three collections, all males, were made by the Levis at Moran,
Teton County, Wyoming, in July and August, 1950. Maximum
length about 8 mm.
UToIuLus LEECHI (Chamberlin)
Nemasoma leechi Chamberlin, 1951. Nat. Hist. Miscellany, No. 87, p. 10,
fig. 20.
JULY, 1954] BELKIN—-MOSQUITO PUPAE 227
Several specimens were collected by the Levis from under rocks
on a dry hillside, altitude 7100 feet, at Sunwapta Pass, Vaspar
National Park, Alberta, Canada, August 10, 1951.
THE DORSAL HAIRLESS SETAL RING OF
MOSQUITO PUPAE
(Diptera: Culicidae)
Joun N. BELKIN
University of California, Los Angeles
The “dorsal hairless setal ring”, as the name implies, resembles
an alveolus of a bristle but lacks a projecting seta. In most mosquito
pupae there is a pair of these structures on the dorsum of each of
the abdominal segments III to V, usually in more or less close
association with one of the regular bristles. In some forms the
“setal ring” is lacking on segment III (Wyeomia) or segment V
(subgenus Rachisoura of Tripteroides) and may be even com-
pletely absent (Trichoprosopon, Sabethes). This “setal ring” has
usually been interpreted as a reduced bristle, and some workers
have been of the opinion that, on segment II it is represented by
a fully developed hair and that on the segments beyond V it has
been completely lost (Baisas, 1938; Edwards, 1941; Penn, 1949;
Darsie, 1949, 1951). Such an opinion appears to be supported by
the fact that in the pupae of many common mosquitoes there is
one more pair of fully developed hairs on the dorsum of segment
II than on the following segments. On the other hand, the above
mentioned workers did not study the chaetotaxy of the venter of
the abdomen and it has been shown by Knight and Chamberlain
(1948) beyond any doubt that the extra hair of the dorsum of
segment II is actually one of the ventral hairs (10) which has
moved dorsad in these forms while in several groups it has re-
tained its primitive ventrolateral opposition (e.g. Chagasia, Sabethes,
Wyeomyia, Limatus, Topomyia, Harpagomyia, Tripteroides [Rach-
isoura], Culiseta, Ficalbia, Aedeomyia, Mansonia, Opifex, Deino-
cerites). Accordingly Knight and Chamberlain assigned the
designation O to the “dorsal hairless setal ring” and did not con-
228 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. Xxx, NO. 3
sider that it was represented by a serial homologue on abdominal
segments II and VI—-VIII. Their inclusion of this structure in the
terminology and its name presupposes that the “setal ring” has
arisen as a modification of a regular bristle. In my review of the
pupal chaetotaxy (Belkin, 1952), I disregarded this structure
completely for it has apparently no homologue in the larva and
does not seem to fit in at all in the general chaetotaxy pattern, but
I failed to indicate my reasons for this action. Additional evidence
is now at hand and indicates that the “setal ring” is probably a
sense organ and has no homology at all with the regular bristles
and should therefore be disregarded in the nomenclature of the
chaetotaxy.
Recently, in studying the pupae of the anophelines of Cali-
fornia, | have encountered a race of A. occidentalis Dyar & Kuab,
1906 in which this “dorsal hairless setal ring” occurs sporadically
on abdominal segment II. Of ten specimens examined two showed
this structure on both sides of the segment and two additional
ones on the right side only. The setal rings are indistinguishable
from those of the following segments, occur in the same position on
the segment, and are located between hairs 4 and 5. This evidence
is a further support for the interpretation that the “setal ring” is
not represented by one of the fully developed hairs on abdominal
segment II, for the hair interpreted as homologous with the setal
ring (hair 4) by Baisas, Penn and Darsie is also fully developed
on segment II along with the “setal ring”.
The question still remains as to the nature and origin of the
“setal ring”. Two general explanations are possible: either it is
developed from a regular bristle or it is a new structure bearing no
relationship to the bristles. The first alternative will be examined
first. There is no way in which the “‘setal ring” can be homologized
directly with any regular hair without disrupting completely per-
fectly evident homologies already established but this structure may
have arisen either as a duplication of one of the hairs or it may
represent one of the transitory larval hairs that are occasionally
carried over to the pupa. I have noted earlier (Belkin, 1952:128)
that both phenomena occur rather frequently in the pupae of some
~ mosquitoes and that some of these anomalous hairs are represented
by alveoli only. In all duplications observed by me the twin hairs
always retain a very close relationship and generally exhibit a
similar degree of development. If the “setal ring” has arisen as
JuLy, 1954.] BELKIN—-MOSQUITO PUPAE 229
a result of the duplication of one of the dorsal hairs, | believe
that it is very likely that it would have remained in close associa-
tion with this hair on all segments and in all mosquitoes. Such is
not the case, for it may be variously associated with hairs 3, 4 or 5
or any combination of these, although it may seem at first glance
to be most frequently associated with hair 5. It appears rather that
the “‘setal ring” has a characteristic position on each segment and
in each group, and that its apparent association with a particular
hair is due secondarily to the presence of that hair in the same
general area. The transitory larval hairs which are occasionally
retained in the pupa are all ventral in position, but there is a
possibility that one of them may have migrated to the dorsal sur-
face as has been the case with hair 10 on abdominal segment II
of some forms. That the “setal ring” could not have arisen through
the retention of one of these transitory hairs is demonstrated in
the pupae of A. occidentalis, A. punctipennis (Say), 1823 and A.
freeborni Aitken, 1939 in which both pairs of transitory hairs may
be occasionally present on the venter while the “setal ring” is
present simultaneously on the dorsum (Belkin, 1953). Finally,
if the “‘setal ring” has arisen as a result of either a duplication or
a retention of a transitory hair one would expect occasional
anomalies of this structure which would be in the form of a reduced
bristle. To date no such anomalies have been seen in the examina-
tion of over a thousand “‘setal rings”. Thus it is probable that the
“dorsal hairless setal ring” is new and peculiar to the pupal stage
and bears no homology to any element of the chaetotaxy. On the
chance that it did arise from one of the bristles, we should watch
for anomalies.
At present nothing is known of the function of the “dorsal
hairless setal ring’’. Its structure suggests a sense organ, possibly
one associated with the orientation and the movements of the pupa,
since it occurs on the segments exhibiting the greatest curvature in
the abdomen. In this connection it is interesting to note that, in
those sabethines (restricted to small containers of water) which
possess very sluggish pupae, it may be completely absent (T'richo-
prosopon, Sabethes) or lacking on II (Wyeomyia) or V (sub-
genus Rachisoura of Tripteroides). It would be of considerable
interest to determine experimentally the function of this structure.
Since the “setal ring” apparently does not represent a reduced
hair and since it appears to be a sense organ, I suggest that the
230 THE PAN-PACIFIC ENTOMOLOGIST [VOL. xxx, NO. 3
cumbersome and ambiguous term “dorsal hairless setal ring” be
dropped in favor of the simpler “dorsal sensillum” and that it
should not be included in the nomenclature of the pupal chaetotaxy.
As pointed out above, its occurrence and distribution may be of
value in separating mosquito groups and therefore it should be
studied and recorded as in the past. ;
ADDENDUM
In June, 1954, William A. McDonald of our Department noted
in the fourth instar larva of Culex tarsalis Coquillett, 1896 a minute
sensillum on abdominal segments IIJ—-V between and slightly
cephalad of hairs 3 or 4. I have examined representative species —
in several genera and have found a similar sensillum in approxi-
mately the same or in a more cephalic, caudal or lateral position.
Since there is a close correspondence between this larval sensillum
and the pupal dorsal sensillum in regard to occurrence on spe-
cific segments and relation to hair 4, I consider these sensilla
homologous.
REFERENCES
Baisas, F. E.
1938. Notes on Philippine mosquitoes VII. Philip. Bur. Health, Month.
B. 18:175—232.
Bevkin, J. N.
1952. The homology of the chaetotaxy of immature mosquitoes and a
revised nomenclature for the chaetotaxy of the pupa. (Diptera,
Culicidae). Proc. Ent. Soc. Wash., 54:115—-130.
1953. Corrected interpretations of some elements of the chaetotaxy of
the mosquito larva and pupa. Proc. Ent. Soc. Wash., 55:318-324.
Darsig, R. F.
1949. Pupae of the anopheline mosquitoes of the Northeastern United
States (Diptera, Culicidae). Rev. de Ent. 20:509-530.
1951. Pupae of the culicine mosquitoes of the Northeastern United
States (Diptera, Culicidae, Culicini). Cornell Univ., Mem. Agr.
Exp. Sta., 304. 67 pp.
Epwarps, F. W.
' 1941. Taxonomy of culicine pupae. In Mosquitoes of the Ethiopian
region. III. Culicine adults and pupae. London, British Museum
(Nat. Hist.) p. 354-428.
Knicut, K. L. anp R. W. CHAMBERLAIN
1948. A new nomenclature for the chaetotaxy of the mosquito pupa, based
on a comparative study of the genera (Diptera: Culicidae). Proc.
Helminth. Soc. Wash., 15:1-10.
Penn, G. H.
1949. The pupae of the mosquitoes of New Guinea. Pacific Sci. 3:3—85.
- A,
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Vol, XXX OCTOBER, 1954 No. 4
THE
PAN-PACIFIC ENTOMOLOGIST
CONTENTS
BEAL—Classification of the dermestid genus Dearthrus with description
Glee Wa STC TOS tea eemte tetas ocean ax eae noe ads one Nete, Sere paced Peat cub chen cesusgeuveanters 231
WILLIAMS—tThe wasps of the genus Pisomopsis..............2:..ccscsscenseseceeeneseeers 235
JAMES—tThe Diptera collected on the Cockerell and Hubbell expedi-
' tions to Honduras. Part III: Tylidae, with a new species from Mexico 247
LEE—First report of Trichocorixa calva (Say) from Mexico...........-.-..------ 250
BERGAMIN-—Utilization of hydroponics in ecological studies of the
cotton aphid
On ee ene eee e een eens newer n ess em en ten sone ans san ssa seg sen torent a8 taeeessescertrceneeunes
BREAKEY—Pit-making pittosporum scale in western Washington.............. 257
KROMBEIN—A new Perisierola from California... ..-..c.--ccecseceeececeseeeees 259
CHAO —Insects in grain elevators at Pullman and Albion, Washington....260
LINSLEY, MACSWAIN, and SMITH—A note on the nesting habits of
Exomalopsis solani -Gockerel) oie. 2 - aosete te wostcmecece oes ionaibeaecwsSesncteansk 263
BOOKING TEC BS oot s tenn caet cere vee ence lees eee erin es dbPoatnoconsoapacks 234, 246, 262
SAN FRANCISCO, CALIFORNIA «+ 1954
Published by the PACIFIC COAST ENTOMOLOGICAL SOCIETY
in cooperation with THE CALIFORNIA ACADEMY OF SCIENCES
THE PAN-PACIFIC ENTOMOLOGIST
EDITORIAL BOARD
E. G. LINsLeY | P. D. Hurp, Jr., Editor R. L. Usincer
E. S. Ross H. B. Leecu
R. C. MILLER, Treasurer A. E. MiIcHELBACHER, Advertising
Published quarterly in January, April, July, and October with Society Proceed-
ings appearing in the January number. Papers on the systematic and biological
phases of entomology are favored, including articles up to ten printed pages on
insect taxonomy, morphology, life history, and distribution.
Manuscripts for publication, proof, and all editorial matters should be addressed
to Dr. P. D. Hurd, Jr., at 112 Agricultural Hall, University of California, Berkeley 4,
Calif. All communications regarding non-receipt of numbers, changes of address,
requests for sample copies, and all financial communications should be addressed
to the treasurer, Dr. R. C. Miller, at the California Academy of Sciences, San
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Domestic and foreign subscriptions, $4.00 per year in advance. Price for single
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Announcing ...
REVISION OF THE SPIDER MITE FAMILY
TETRANYCHIDAE
by A. Earl Pritchard and Edward W. Baker
This world-wide treatment (300 pp., 330 figures) of the “Red
Spiders” is the second volume in the Memoirs Series of the Pacific
Coast Entomological Society. Each species is beautifully illustrated
in the inimitable style of E, W. Baker. The work deals with the
systematics, identification, and economics of the “Red Spiders”.
Synoptic keys have been prepared, descriptions are presented for
all species including the major agricultural pests, and some twen-
ty species are described as new.
Publication date—December, 1954.
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Send orders to: Treasurer, Pacific Coast Entomological Society,
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Entered as second class matter, February 10, 1925, at the post office at
San Francisco, under act of August 24, 1912.
The Pan-Pacific Entomologist
Volume XXX October, 1954 No. 4
CLASSIFICATION OF THE DERMESTID GENUS DEARTHRUS
WITH DESCRIPTION OF A NEW WESTERN SPECIES
(Coleoptera )
R. S. BEAL, JR.
Denver, Colorado
Specimens of Dearthrus are not at all common in collections,
and almost nothing is known of their biology. However, a few of
them have been brought to my attention, and a study of these has
shed some light on their previously obscure relationships. Al-
though the immature stages are still unknown, the adults seem to
exhibit characters which definitely warrant placing the genus in a
subfamily different than that to which it is commonly assigned.
The: genus seems unquestionably to belong to the subfamily
Megatominae rather than to the Attageninae. It has been considered
in the Attageninae because of the place assigned to it in Casey’s'
key, where it is grouped with genera having the first metatarsal
segment decidely shorter than the second. This is not true of
Dearthrus, the first segment being subequal to the second. Further,
in the shape of the metacoxal lamina it is unlike any representative
of the Attageninae which I have seen. In Attagenus and in Novelsis
the metacoxal plate bears a distinct tooth or is distincly broadened
laterad to the insertion of the femur. In Dearthrus, as in Megatoma,
Trogoderma, Globicornis, and so on, the metacoxal lamina is
gradually narrowed laterally. Finally, the general facies are quite
like those of the Megatominane, particularly of certain sections of
Globicornis. Casey’s use of the lateral extension of the metacoxal
plates as a tribal character is apparently of little value. In Dearth-
rus the metacoxa reaches the inner posterior angle of the mete-
pimeron. However, this is true of some sections of the Attageninae
as well as of the Megatominae. Likewise the number of segments in
the antenna is of little significance above a subgeneric level, since
this character shows considerable variation throughout the family.
Whether the genus should be synonymized with Pseudomesalia
Ganglbauer is a question which will have to await a closer study of
1T. L. Casey, 1900. Review of the American Corylophidae, Cryptophagidae,
Tritomidae, and Dermestidae and other studies. Jour. N. Y. Ent. Soc., 8:144.
232 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
the latter. Kalik? has recently described a species belonging to this
sroup, Globicornis (Pseudomesalia) kulti, including figures of the
adult and of the antenna of a specimen which he questionably con-
siders to be a female. The pubescence and configuration of the
adult are quite similar to our species of Dearthrus. The antenna is
nine-segmented and bears a large terminal segment which is much
larger than the seventh and eighth segments. The shape of the
antenna of Dearthrus, and suggests the possibility that these
the Megatominae. If the antenna figured by Kalik is indeed that of
a female, then Pseudomesalia and Dearthrus are most likely dis-
tinct. However, its configuration does closely resemble the male
antenna of Dearthrus, and suggests the possibility that these
groups are identical.
Dearthrus longulus LeConte of the eastern United States is the
only species of the genus known at present. A second species oc-
curing in the inland mountains of California and Oregon should
also be recognized. I am happy to be able to name this species for
an able student of systematic zodlogy, Dr. Robert C. Stebbins of
the University of California at Berkeley.
Dearthrus stebbinsi Beal, new species
Adult male—Body long and narrow with sides subparallel; elytra
slightly expanded behind middle. Color of head and pronotum black; elytra
dark brown; undersurfaces dark brown with legs somewhat lighter. Pubes-
cence of dorsal surfaces dark brown, short, moderately fine, subrecumbent;
pubescence of ventral surfaces dark golden brown, short, fine, appressed.
Punctation of head and pronotum shallow, umbilicate, with punctures three
to four times as large as facets of eye, confluent on head and sides of pro-
notum, contiguous on disc of pronotum; punctation of elytra craterform with
punctures one to two times as large as facets of eye and separated by one to
two diameters of one puncture. Antennae in repose extending nearly to base
ef prothorax; configuration as illustrated (except that ultimate segment of
holotype two and one-half times as long as wide); ultimate segment of
antenna densely clothed with very fine erect hairs about two thirds as long
as width of third segment of antenna. Prosternal process long, narrow, with
sides parallel to apex. Mesosternal sulcus very shallow, becoming evanescent
posteriorly; mesosternum emarginate posteriorly between mesocoxae. Length
(of pronotum and elytra): 2.7 mm. Width (at humeri): 1.1 mm. |
Adult female.—Configuration of antenna as illustrated; antennal club
more sparsely covered with fine hairs of irregular but generally longer length
than those of male.
?Viadimir Kalik, 1949. New Dermestidae of the Palearctic fauna. Acta Ent.
Mus. Nat. Pragae, 26(362) :1-4.
OctTosBer, 1954] BEAL—-DEARTHRUS 233
Range of observed variations.—Color of elytra and undersur-
faces varying from dark brown to black. Ultimate segment of male
antenna varying from twice as long as wide to three times as long
as wide. Length (of pronotum and elytra) varying from 3.0 mm.
to 2.4 mm. Ratio of length to width varying from 1:0.41 to 1:0.47.
ee \ Male Female
Fig. 1, Antennae of Dearthrus stebbinsi
Holotype male and allotype female (deposited in California
Academy of Sciences): Mariposa County, CaLirornia, June 3,
1914 (F. W. Nunenmacher). Paratypes as follows: California:
Yosemite Valley, one male, June 5, 1930, and two females, June 9,
1930 (F. E. Blaisdell) ; Yosemite Park, one male, 1922 (Chas.
Veatch) ; Sierra Meadow, Giant Forest, one male, July 1, 1928
(EZ. A. McGregor) ; Tahoe, one female, July 7, 1915 (R. Hopping) ;
Bass Lake, one female, June 3, 1942 (A. J. Walz); Plummer
Springs, Trinity County, one female, June 23, 1919 (R. Hopping) ;
Fowlers Camp, Siskiyou County, two females, July 2, 1946 A. T.
McClay) ; Bridge Camp, Shasta County, one male and two females,
June 2, 1946 (A. T. McClay). Oregon: Eight miles northwest of
Sisters, one female, July 8, 1939 (Schuh and Gray).
The holotype of stebbinsi bears two indentations on the disc
of the pronotum. Similar indentations have been used as a tax-
onomic character in other dermestids. However, in this species the
indentations occur in only a few of the specimens, and are probably
not of genic origin.
D. stebbinst and D. longulus are easily separated on the basis
of several characters. The punctures on the disc of the pronotum of
longulus are small, each puncture being one and one half to two
times as large in diameter as a facet of the eye, and individual
puntures are separated by one or two diameters of one puncture.
In stebbinsi the puntures are twice as large and are contiguous.
The ultimate segment of the female antenna of longulus is ap-
proximately three fourths times as long as wide. In stebbinsi the
ultimate segment of the female antenna is at least one and one
third times as long as wide, The ultimate segment of the male
234: THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
antenna of longulus, according to Casey’s illustration, is but one
and one third times as long as wide. The ultimate segment of the
male antenna of stebbinsi is two to three times as long as wide. The
mesosternal sulcus of longulus extends the entire length of the
mesosternum and is quite distinct, while that of stebbinsi is shallow
and obliterated posteriorly.
Details of the biology of stebbinsi are unknown, except that
one specimen was collected on Ceanothus at Bass Lake, California
(A. J. Walz).
For material used in this study I wish to express my thanks
particularly to W. H. Anderson, P. D. Hurd, Jr., J. N. Knull, H. B.
Leech, A. T. McClay, G. E. Wallace, and A. J. Walz.
BOOK NOTICE
FLEAS, FLUKES & CUCKOOS. By Miriam Rothschild and Theresa Clay.
304 pp., 99 black and white photographs (= pls. I-XL), 4 maps, 22
drawings.-Collins, St. James Place, London; The Philosophical Library,
Inc., 15 East 40th St., New York 16, N. Y. 1952.
The cover title may puzzle some people, but the content will delight
every naturalist and most other readers. The exquisite choice of words makes
plain sentences stick in one’s memory. Statements of fact which might be
elsewhere dry, remain accurate yet often become excruciatingly funny. Specu-
lation is clearly noted as such.
The book tells of the parasites of birds, which include fleas, feather lice,
protozoa, worms, flies, mites and ticks, and “micro-parasites” (bacteria,
viruses, fungi). Discussions of these in the above order, fill chapters 7—13,
and comprise most of parts II and JI. Part I is introductory, and treats of
parasitism, commensalism, symbiosis, the effect of parasites on the host and
of parasitism on the parasites, the origins of parasitism, and the evolution of
parasites. The final chapters of part III deal with the fauna of birds’ nests,
the clepto-parasitic skaus, and the parasitic European cuckoo. Throughout
there are pointers to unanswered or unexplored problems, both in entomology
and in ornithology. There is a general index and one of scientific and popular
names. The photographs and line drawings are almost all excellent and have
been discriminatingly chosen. The book deserves its rank of a Special Volume
in the New Naturalist series—Hucu B, Leecu,
OcTroBer, 1954] WILLIAMS-—PISONOPSIS 055
THE WASPS OF THE GENUS PISONOPSIS FOX
(Hymenoptera: Sphecidae)
Francis X. WILLIAMS
Research Associate, Department of Entomology
California Academy of Sciences
The material studied consists of 93 specimens. Seven of these
are from the collection of the United States National Museum and
from that of Dr. Karl V. Krombein; 3 are from Dr. G. E. Bohart’s
collection; 37 from the California Insect Survey, Department of
Entomology and Parasitology, University of California; 2 from
Mr. P. H. Timberlake; 3 from the California Academy of Sciences;
1 from the American Museum of Natural History; 3 from P. W.
Weber of Honolulu; and 37 are of my own collecting. Three
species and two subspecies are represented, as follows:
Pisonopsis clypeata Fox. Nevada and California.
Pisonopsis clypeata occidentalis Williams, California.
Pisonopsis birkmanni Rohwer. Texas and California.
Pisonopsis triangularis Ashmead. Colorado, Wyoming, Idaho and Cali-
fornia.
Pisonopsis triangularis californicus Williams, California.
The only other species of Pisonopsis that appear to be described are:
Pisonopsis anomala Mantero, 1901, Bul. Soc. Ent. Ital., 33:202—203. From
Argentina (Patagonia).
Pisonopsis argentinus Schrottky, 1909, An. Soc. Cien, Argentina, 68:
249, From Argentina (Catamarca).
Thanks are due to the above institutions and entomologists for
the loan of material, and particularly to Dr. Karl V. Krombein
of the United States National Museum for comparing certain of
the specimens.
Genus Pisonopsis Fox
Pisonopsis Fox, 1893, Psyche, 6:553. Genotype, Pisonopsis clypeata,
from Nevada.
Form stout; mandibles notched beneath, no malar space; eyes moderately
emarginate within in female, rather weakly so in the male; interocular space
at clypeus usually distinctly greater than at vertex; ocelli round; antennae
placed immediately behind clypeus; prepectus present; marginal cell not
appendiculate though terminating rather bluntly on costa, not or hardly
extending beyond third submarginal cell; second submarginal cell rather
short petiolate, usually receiving both recurrent veins; anal lobe of hind
wings short, not at all reaching to opposite the apex of submedian cell; legs
not strongly spinose; middle tarsi with one apical spur; tarsal claws entire,
somewhat inflated basally beneath. Female with or without a margined
236 THE PAN-PACIFIC ENTOMOLOGIST [ VoL. xxx, No. 4
pygidial area, and without a tarsal comb. Tergites somewhat constricted
apically.
This small American genus is somewhat related to Pison, which
however, does not have the mandibles notched beneath, while the
eyes are deeply notched within, the marginal cell is long and
lanceolate and the stigma is longer.
There is a group of tropical American wasps somewhat inter-
mediate between Pisonopsis and Pison, and of which | have taken
two species representing oriental Ecuador, British Guiana and
Brazil. Here the eyes are deeply emarginate and the marginal
cell as long as in Pison, but the mandibles are strongly notched
beneath as in Pisonopsis.
Little seems to be known about the life history of Pisonopsis.
Linsley et al' report (p. 274) finding four species of wasps of
the family Larridae (two species of Solierella and two of Pison-
opsts) appropriating the burrows of the Diadasia bee for their
nests. These authors state: “One species in particular, Pisonopsis
clypeata Fox, was very abundant, and females were commonly ob-
served entering both old and new bee burrows. When the first
30 burrows constructed in the square yard area were dug out at
the end of the active season, five were found to have larrid pro-
visions in the entrance tube.” ... “The Pisonopsis does not alter
the original dimensions but accumulates small pebbles and wood
fragments to separate its several young.” The nature of the prey
of these Pisonopsis was not determined.
Early in the summer of 1952 the writer reared seven individuals
of Pisonopsis birkmanni from two lots of cocoons found in small
dead stems of poison hemlock (Conium maculatum L.) collected
during the winter at Danville, Contra Costa County, California.
The cells were separated chiefly by grains of soil, and the casks
or cocoons much resemble those of Solierella save that those of
Pisonopsis have a somewhat shining resinous appearance instead
of being entirely granular, as in Solierella. The cask of Pisonopsis
may be imperfectly enveloped in a loose mantle of soil grains.
Remains of crab spiders (Thomisidae) were found in one of these
nests.
Later in the summer of 1952 I secured another nest from a
1 Linsley,, E. G., MacSwain, J. W., and Ray F. Smith, 1952, The Bionomics of
Diadasia consociata Timberlake and some biological relationships of Emphorine
and Anthophorine bees, U. C. Pub. Ent., 9(8) :267-290, plates 1-6.
Octoper, 1954] WILLIAMS—PISONOPSIS 237
SS
ee
SS
a
Fig. 1. Pisonopsis clypeata subspecies occidentalis. Male. Length 6.5 mm.
From San Rafael, California. Fig 2. Same. Male. Aedeagus. Fig. 3. Same.
Male. Antennal segments 3 and 4 and 4-6. Fig. 5. Same. Male. Last visible
ventral segment. Fig. 6. Pisonopsis triangularis subspecies californica. Male.
Fig. 7. Pisonopsis clypeata. Female. Pygidium. Gold Lake, Mono County,
California. Fig. 8. Pisonopsis clypeata subspecies occidentalis. Female. Pygid-
ium. San Rafael, Marin County, California. Fig. 9. Pisonopsis triangularis
subspecies californica. To show poorly defined pygidial area. Tassajara Hot
Springs, Monterey County, California.
238 THE PAN-PACIFIC ENTOMOLOGIST [ VoL. xxx, No. 4
stem of a clump of oats, the stem was cut down to about four and
one-half inches from the ground a few days previous. The upper
cell was stoppered to the brim as well as separated from the
second by considerable quantities of fine soil lumps. It contained
25 generally pallid thomisid spiders, the largest about 3 mm.
long. On one of the innermost of these spiders a small wasp larva
was feeding. A few days later both cells contained typical Pisonop-
sis casks. Still later in the summer other such nests were found
under the same conditions.
During the summer of 1953, several individuals of Pisonopsis
birkmanni were reared from cocoons found in dead stems of the
white sage (Salvia apiana Jepson), collected. at La Mesa, San
Diego County, California.
Key To THE Species OF NortH AMERICAN PISONOPSIS
1 Antennae with 12 segments; abdomen with 6 tergites visible (females)
ob Ales 2:
— Antennae with 13 segments; abdomen with 7 tergites visible (males)
apices 6
2. Pygidium well defined, margined by a carina; sculpture coarser; abdo-
THEM SAT GEC, GOR MESS vale te 3 Sneha de Cove CES Dear ok ee, Senet Saree, | 3
— Pygidium not or poorly defined, there being no bounding carina; sculpture
anenrcabdomencolacky Gnereddisht. <<. Pe ae Beh ee 4
3. Pygidium broader, forming an angle of about 58°—63° ........ clypeata Fox
— Pygidium narrower, forming an angle of about 48°... eee
Pte tA Meat en oA Tota) eee Newt Ped clypeata Fox, subspecies occidentalis Williams
4. Disc of propodeum with a shining, nearly smooth slightly bossed area on
each side of the transversely striated depression, the striae and some
strong punctures somewhat invading this bossed area; on sternites 3, 4, and
to a less extent on 5, is a pair of slit-like grooves that are best developed
laterally, the lamellae nearly joining to form an angle along the middle
line (fig. 27) ; pygidium not at all defined; pronotal lobes pale margined
Rept URN AM Re RIN RSE, lee iets Wik Pear |e Pe ae Me birkmanni Rohwer
— Disc of propodeum of a duller and more rugulose appearance, transversely
striated over the depressed triangular area, and more finely so across the
slightly bossed area on either side, and with no distinct strong punctures
invading (fig. 31); sternites 3 and 4 with the grooves becoming weak or
disappearing towards the middle line where they tend to form a lobe
(fig. 28; pygidial area indicated by a slight dorsal flattening and some-
times by a slight latero-apical compression (fig. 9) ....2.2....-eceeeeeeeeeee BY
5. Sternites 3 and 4 with the grooves extending mesad or nearly, as lines;
abdomen “often xeéddishs 29.728 2 Ae 4 triangularis Ashmead
Sternites 3 and 4 with the grooves short, only lateral...
Pn be lee ge aS Dank Ae iriangularis Ashmead, subspecies californica Williams
6. Form stouter, punctures coarser; scutum and scutellum polished, with
large separate punctures; abdomen reddish
Ocroser, 1954] WILLIAMS—PISONOPSIS 239
Fig. 10. Pisonopsis clypeata subspecies occidentalis. Male. Ocelli. Bryson.
Monterey County, California. Fig. 11. Pisonopsis triangularis subspecies cali-
fornica. Female. Monterey County, California.
Figure 12. Pisonopsis clypeata. Female. Posterior coxa, to show carinal
lobe. Mono County, California. Fig. 13. Pisonopsis triangularis subspecies
californica. Female. Posterior coxa, to show carinal lobe. Monterey County,
California. Fig. 14. Pisonopsis birkmanni. Male. Extremity of aedeagus. Menlo
Park, California. Fig. 15: Pisonopsis clypeta, subspecies occidentalis. Male.
Extremity of aedeagus. Fig. 16. Pisonopsis triangularis, subspecies californica.
Female. Monterey County, California. Fig. 17. Pisonopsis triangularis subspe-
cies californica. Male. Antennae, two views. Lassen County, California.
240 THE PAN-PACIFIC ENTOMOLOGIST [ VoL. xxx, No. 4
— Form less stout; clypeus always triangularly produced; puncturation
finer; scutum and scutellum with punctures on what appears to be in
certain lights, a very finely reticulate surface; abdomen black or reddish
a nee res J Nb sea A Lede 2 A ed le ah ee A nee 8
7. Clypeus triangularly produced or with a gradation slightly indicated
Girne ek Aty BLES cob dt e.g rhe ete Be ae oO ck Rie We clypeata Fox
— Clypeus truncate, with a median tooth (figs. 22, 23) W.....-.-.----2--------2--0---+-
VP MASEAS) | vls) 0 coche Seal clypeata Fox, subspecies occidentalis Williams
8. Vertex, and dorsum of thorax with strong close punctures, the punctures
behind the ocellar area often not or hardly their own diameter apart;
disc of propodeum with the median striated area not much depressed,
bordered laterad by a shining though more or less transversely striated
area, with few strong punctures invading from the sides; no median carina;
slit-like grooves on sternites 3 and 4 forming an angle mesad; pronotal
lobes narrowly pale margined ...........---.--------...------ .... birkmanni Rohwer
— Vertex and dorsum usually with somewhat finer puncturation, the punc-
tures behind the ocellar area often much more than their diameter apart;
disc of propodeum with the median area well depressed and with a carina,
the whole glabrous area obliquely and transversely striate; slit-like grooves
on sternites 3 and 4 either rudimentary or uniting mesad as a rounded
lobe; pronotal lobes entirely black 0.20..0........c..-....ccececcecesceeseenecesenceceecees 9
9. The slit-like grooves on sternites 3 and 4 well developed; meeting or
nearly meeting at the middle line to form a lobe; abdomen sometimes
actly ake detec hehe ao FO ee ER neta 28S triangularis Ashmead
- The slit-like grooves poorly developed, short and far laterad, present on
Stee Oy Oo AN GRAS Ln Se Bi le NY pene Re SERS eae ae ee
RELIC 1 Se Meat 4 triangularis Ashmead, subspecies californica Williams
PISONOPSIS CLYPEATA Fox
(Figures 7, 12, 19, 30, 32)
Fox, 1893, Psyche, 6:553-554. Male and female. Nevada (Morrison).
Female: Length 9 mm. Stout, rather coarsely sculptured, shining. Black;
abdomen rufous. Clypeus drawn out wedge-like. Strong distinct punctures
on head and dorsulum; disc of propodeum with a somewhat triangular en-
closure, obliquely striate on basal portion, transversely so on apical portion.
Pygidial area triangular, well margined and with strong punctures. Pile
silvery.
Male: Length 7 mm. Much like the female, but segments 1-6 of the
flagellum of the antennae produced beneath; the clypeus is produced wedge-
like but with an indication of gradation (fig. 30). Pygidium densely though
rather irregularly rugulosely punctuate; last visible ventral segment rather
broadly excavate. Pile silvery.
Through the kindness of Mr. J. A. G. Rehn, of the Academy
of Natural Sciences of Philadelphia, I was able to study a male
and a femal of the type series. I have also seen a single female from
Gold Lake, Sierra County, California, collected August 2, 1921,
by C. L. Fox (California Academy of Sciences). The pygidium
OcroBerR, 1954 | WILLIAMS—PISONOPSIS 241
Fig. 18. Pisonopsis triangularis subspecies californica. Female. Monterey
County, California. Fig. 19. Pisonopsis clypeata. Female. Mono County, Cali-
fornia. Fig. 20. Pisonopsis clypeata, subspecies occidentalis. Female. San
Rafael, California. Fig. 21. Pisonopsis birkmanni. Female. San Mateo, County,
California. Fig. 22. Pisonopsis clypeata, subspecies occidentalis. Male. San
Rafael, California. Fig. 23. Same. Male. Bryson, Monterey County, Califor-
nia. Fig. 24. Pisonopsis triangularis, subspecies californica. Female. Clypeal
outline. Mt. Lassen, California. Fig. 25. Same. Female. Mandible, outer side.
Fig. 26. Pisonopsis clypeata, subspecies occidentalis. Female. Clypeus un-
worn. Near Palm Springs, California.
242 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
and head are shown (figs 7 and 19, respectively) ; this specimen,
however, has the pygidium narrower than in the type (fig. 32),
and thus approaching that of its subspecies (fig. 8).
Pisonopsis clypeata occidentalis Williams, new subspecies
(Figures 1-5, 8, 10, 15, 20, 22, 23, 26, 29)
Female, holotype: Length 7.75 mm. Black, moderately shining, strongly
punctate and sculptured, the two basal joints of the antennae in part, and
the apical half of the mandibles reddish brown, hind margin of pronotal
lobes whitish, tegulae, axillary sclerites and base of wings more or less
brownish, abdomen orange red, the somewhat apical margin of the segments
testaceous. Clypeus produced subconic, the disc subconvex, not carinate,
with coarse punctures before the smooth depressed apical portion; antennae
rather slender, segments 3 and 4 subequal; frons very densely punctate-granu-
late; vertex with strong close punctures; interocular space at vertex about
.70 of its narrowest width at clypeus and about equalling antennal segments
2 plus 3 plus 4; ocelli forming nearly a right angle triangle; a depressed
line from anterior ocellus to about abreast of the ocular emargination. Scu-
tum, mesopleura and scutellum with strong separate punctures; postscutel-
lum fine, very close ones; propodeum with an inbowed triangular depression
with a median carina and well-spaced oblique and transverse carinulae, the
rounded ridges laterad transversely striate; laterad of these ridges granulate,
the pleura with strong horizontal striae, the posterior face striato-granulate
and with a median groove. Posterior coxae with a rounded ridge on inner
side above near base. Second submarginal cell receiving both recurrent
veins. Abdomen with strong separate punctures; pygidium with the lateral
carinae sharp, the disc. with fine close punctures and somewhat depressed and
constricted beyond middle length. Vestiture rather sparse silvery pile.
Male, allotype: Length 7 mm. In general resembling the female, but
the apical half of the abdomen, except for the testaceous margin of the seg-
ments, is blackish. The clypeus is subtruncate, with a median tooth, its disc
closely punctate; antennae with segments 3-6 nearly equal, segments 3 and
4 excavate beneath and somewhat inwardly at base and there polished and
with fine erect pile; segments 4-9 beneath and somewhat outwardly, pro-
duced so as to give that section a more or less spirally crenulate appearance.
Interocular space at vertex relatively broad, about .80 of the space near the
clypeus and slightly greater than antennal segments 2 plus 3 plus 4. Pygidial
area flat, not margined, densely punctuate.
Holotype female and allotype male (California Academy of
Sciences): SAN RaraEL, Marin County, Cauirornia, July, 1922
(F. X. Williams), on ground among dry leaves at edge of thicket.
Paratypes: 1 female and 10 males, San Rafael and nearby, July 16
and 22, 1922 (F. X. Williams) ; 1 male, Bryson, Monterey County,
California, May 18, 1920 (E. P. Van Duzee) (Collection. Cali-
fornia Academy of Sciences) ; 1 female near Palm Springs, River-
side County, June 8, 1930 (P. H. Timberlake), on Eriogonum
£
Ocroser, 1954] WILLIAMS—PISONOPSIS 243
trichopodum; other specimens: 11 females and 22 males, Tracy,
San Joaquin County, end of May, in June, and August 1, 1949
(J. W. MacSwain, R. F. Smith and P. D. Hurd) ; 1 male, Tanbark
2
va
a
9
Fig. 27, Pisonopsis birkmanni. Male. To show grooves on sternites 3-5.
Williamson County, Texas. Fig. 28. Pisonopsis triangularis. Male. To show
grooves on sternites 3 and 4. Green River, Wyoming. Fig. 29. Pisonopsis
clypeata, subspecies occidentalis. Female, Clypeus, unworn but not the usual
type. Tracy, California. Fig. 30. Pisonopsis clypeata. Male. Allotype. Clypeus.
Nevada. Fig. 31. Pisonopsis triangularis, subspecies californica. Female type.
Disc of propodeum. Summit Lake, Mt. Lassen, California. Fig. 32. Pisonopsis
clypeata, Paratype female. Pygidium. Nevada.
244. | THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
Flat, San Gabriel Mountains, California, June 25, 1950 (F. X.
Williams).
This subspecies differs from typical P. clypeata Fox by the
narrower pygidium of the female, and by the distinctly truncate
and toothed clypeus (with slight variations) in the male.
The female paratype and all the males have the apex of the
abdomen blackish.
PISONOPSIS BIRKMANNI Rohwer
(Figures 14, 21, 27)
Rohwer, 1909, Trans. Amer. Ent. Soc., 35:129. Female. Lee County,
Texas, (Birkmann).
Descriptions based on California specimens: Female: Length 6. mm.
Black; head and thorax subopaque, disc of propodeum with a shining area
each side of the median sulcation; mandibles reddish on apical half, prono-
tal lobes white to pale brownish apically. Clypeus with the convex basal
part coarsely punctate, particularly at the origin of the smooth produced
median portion which forms a wedge which is slightly shouldered not far
far from the apex; antennae short, segment 4 slightly longer than 3; front
and vertex opaque, finely reticulate and granulate-punctate; ocelli forming
a right angle triangle; interocular space at vertex little if any narrower than
at clypeus. Dorsulum appearing reticulate and with rather fine strong punc-
tures, sparser on scutellum. Disc of propodeum with an inbowed, somewhat
trianguler depressed area, its median carina not strong, the fine oblique
carinulae becoming transverse at apex of disc; a finely reticulate shining
strip on either side on disc, with strong, well-separated punctures invading
from the striato-punctate area of most of the pleura and posterior face; the
posterior face has on inverted, narrowly tear-shaped trench; posterior coxae
with a rounded basal lobe. Abdomen with strong punctures, finer on apical
segments, the apical margin of the sternites more or less testaceous; pygidium
not margined, the area finely and closely punctate; sternites more finely
punctate; pile silvery.
Male: Length 5.25 mm. About like the female. Clypeal tooth acute;
antennal segments 3 and 4 subventrally excavate at base, this area brown
and shining, while dorsally there is some fine erect pile; antennal segment
5 somewhat longer than 4, segments 4-9 outwardly convex so as to give that
section a somewhat crenulate effect. Disc of propodeum with the transverse
carinulae more extensively invading the nearly smooth area on either side;
median carina obsolescent. First recurrent vein received at tip of first sub-
marginal cell.
One female and 2 males, Menlo Park, San Mateo County, California,
July 1937 (F. X. Williams); 1 male, Searsville Lake, San Mateto County,
June 29, 1937 (F. X. Williams) ; 6 females and 3 males, Danville, and 1
female, Mt. Diablo, Contra Costa County, California, June—August, 1949
(F. X. Williams) ; 2 males, Tanbark Flat, San Gabriel Mts., California, July
8, 1950 (F. X. Williams) ; 2 males and 2 females, La Mesa, San Diego County,
Summer of 1953 (F. X. Williams) ; 1 male and 1 female, Davis, Yolo County,
OcToBErR, 1954] WILLIAMS—PISONOPSIS 245
California, August 24, 1939 (G. E. Bohart); 1 female, Box Canyon, River-
side County, California, April 13, 1934, on Chilopsidis linearis (Oroban-
chaceae), (P. H. Timberlake) ; 2 females and 1 male, Riverside, September
21, 24, 26, 1948, “feeding at exudations of Opuntia plants” (P. W. Weber).
Other specimens seen: From the United States National Museum and the
Krombein collection, 1 female, Brazos County, Texas, July 25, 1937 (J. E.
Gillaspy), “on corn.” (Dr. Krombein kindly compared this specimen with
the type) ; 1 male, Williamson County, Texas, April 23, 1935 (J. E. Gillaspy) ;
1 female, La Crescenta, Los Angeles County, California (R. M. and G. E.
Bohart), this last specimen not being typical.
This species varies somewhat in sculpture and venation,
PISONOPSIS TRIANGULARIS Ashmead
Ashmead, 1899, Ent. News, 10:9. Female. “Hab. Colorado. Carl C.
Baker Collection, No. 2061. Type, No. 5064, U.S.N.M.”
The type is 6 mm. long, rather opaque, and closely punctate.
The clypeus has a median triangular production, and the disc of
the propodeum is transversely striate, and rugulose. The sinuate
slit-like grooves on sternites 3 and 4 extend nearly or quite to
the median line to form a rounded lobe. The male much resembles
the female; the clypeus has a smooth acuminate point, while the
antennal modifications resemble those of its subspecies, Pisonopsis
triangularis californica (fig. 17) that follows. Figure 28 is from
a male specimen from Green River, Wyoming (4747:American
Museum of Natural History). Other specimens are: 1 male, Tracy,
San Joaquin County, California, May 31, 1949 (J. W. MacSwain) ;
1 female and 6 males, Tanbark Flat, San Gabriel Mountains, Cali-
fornia, 2700 ft., end of June to early July, 1950 (F. X. Williams).
The California specimens have the abdomen largely reddish.
Pisonopsis triangularis californica Williams, new species
(Figures 6, 9, 11, 13, 16, 17, 18, 24, 31)
Female, holotype: length 6.75 mm. Black, moderately shining, frons sub-
opaque; puncturation fine and close; mandibles reddish, subapically; de-
pressed apices of tergites in part testaceous; calcariae brownish to black.
Clypeus with the anterior part of the convex disc with rather large, well-
spaced punctures, the triangular projection smooth; frons finely and closely
punctate; antennal segments 3 and 4 subequal; interocular space at vertex
less than at clypeus; ocelli in less than a right-angle triangle. Dorsum finely
and closely punctate; scutum with a shallow median groove. Disc of propo-
deum shining, the depressed triangular area inbowed, the slope of the depres-
sion gradual, the oblique carinulae well spaced, fanning at base and becoming
transverse and more crowded towards the apex, these carinulae breaking up
towards the pile, the pleura are striato-punctate and the posterior face rugu-
lose and with a smooth subtriangular fovea. Second recurrent vein barely
within the second submarginal cell. Abdomen with fine piliferous punctures;
246 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
pygidial area feebly indicated by a dorsal flattening and slightly compressed
apical sides; sternites 3 and 4 with the slit-like pockets lateral only, indicated
by a fine curved linear groove.
Male, allotype: Length 5.5 mm. Resembling the female in most points.
The clypeus is more sharply pointed, and the rather stout antennae (some-
what less modified than in Pisonopsis birkmanni) have segments 3 particularly, ,
and 4 smooth and constricted for nearly the basal half, with segment 4 notched
dorso-laterad, and segments 5 to 8 in a diminishing degree outwardly rounded
beneath.
Holotype female, allotype male, one female and 1 male para-
type, SummMiT Lake, Lassen County, Catirornia, 6700 ft., July
21, 1937 (F. X. Williams). In good condition. Other paratypes:
1 female, Tassajara Hot Springs, Monterey County, California,
May 18, 1920 (L. S. Slevin) (C.A.S.); 1 female, Mammoth Lake,
Mono County, California, July 25, 1936 (R. M. & G. E. Bohart),
these two specimens having the abdomen somewhat reddish.
This rather weak and variable subspecies differs from Pisonop-
sis triangularis chiefly in the less developed grooves on sternites
3 and 4, and sometimes in its more closely aligned carinulae in the
somewhat less sharply depressed propodeal enclosure.
I am indebted to Dr. Karl V. Krombein for comparing a female
topotype of this subspecies with the type of Pisonopsis triangularis
in the United States National Museum.
BOOK NOTICE
THE TAXONOMY, PHASES, AND DISTRIBUTION OF THE GENERA
CHORTOICETES BRUNN. AND AUSTROICETES UV. (Orthoptera:
Acrididae). By K. H. L. Key. 237 pp., 40 figs., 45 tables. Offset.
Division of Entomology, Commonwealth Scientific and Industrial Re-
search Organization, Australia. Canberra, May 1954. (Order from C. S.
& I. R. Organization, 314 Albert St., East Melbourne, C.2.)
The genera Chortoicetes and Austroicetes include the chief injurious
Acrididae of southern Australia. This paper is a detailed taxonomic study of
the adult grasshoppers, based on very large series, with the results of many
years of field work to aid in interpreting the tremendous infraspecific varia-
tion. Much of the resulting data are given statistical treatment. Three new
species are described, and Latinized names proposed for 11 new forms
(homologous-genetic variations). “ . . . subspecies are recognized only
where the population of a significant geographical region is homogeneous for
a particular character or character complex, which serves to differentiate
every member of that population from the members of other populations
similarly homogeneous for some other character or character complex. The
question is discussed in greater detail in Section III 2 (d).’—Hucu B. Lercu
OcTOBER, 1954] JAMES—TYLIDAE 247
THE DIPTERA COLLECTED ON THE COCKERELL
AND HUBBELL EXPEDITIONS TO HONDURAS
Part Ill: TYLIDAE, WITH A NEW
SPECIES FROM MEXICO!
Maurice T. JAMES
State College of Washington, Pullman
The present paper lists the Tylidae (—Micropezidae) in the
broad sense, including the Taeniapterinae and Neriinae, of the
Cockerell and Hubbell Honduras collections. No Trepidariinae
(—Calobatinae) were encountered. An extralimital species, from
Mexico, is included for want of a better place to. describe it.
Taeniaptera lasciva (Fabricius), 1798, Entomologia System-
atica, Suppl., p. 564 (Musca). Escuela Agricola, Zamorano: Nov.
20, 1946 (Pelen), 1 female; Nov. 24, 1946 (W. P. Cockerell), 1
female; Dec. 27, 1946 (T. D. A. & W. P. Cockerell), 1 male, 2
females; Oct., 1946 (Cisneros), 1 male; Aug. 19, 1948, reared
sweet potato, #236 (Hubbell), 15 specimens; July 9, 1948, tall
weeds, #45 (Hubbell), 1 male, 1 female; July 1, 1948, roadside,
#10 (Hubbell), 1 female; July 19, 1948, weed thicket, #106
(Hubbell), 1 female; July 16, 1948 (Hubbell), 1 male. Rio Claura,
April 13, 1923, #259 (Hubbell), 1 female.
T aeniaptera latitibia (Enderlein) 1922, Arch. fiir Naturgesch.,
88 (A,5), p. 220 (Grallomyia). Tela, Lancetilla, July 28, 1948
(Hubbell), 1 male. |
Tylos (Neriocephalus) stigmaticus (van der Wulp), 1897,
Biologia Centrali-Americana, 2, p. 366 (Micropeza). Escuela Agri-
cola, Zamorano: Nov. 25, 1946 (W. P. Cockerell), 1 male; on bean,
July 19, 1948, #107 (Hubbell), 1 female; meadow, Yeguare River,
~ July 2, 1948, #18 (Hubbell), 1 male; roadside, July 1, 1948, #10
(Hubbell), 1 male, 1 female; July 15, 1948, #77, (Hubbell), 1
male; on gardenia, July 4, 1948, #25 (Hubbell), 2 males.
Tylos abbreviatus (Cresson), 1926, Trans. Amer. Ent. Soc.,
52, p. 262 (Micropeza). Escuela Agricola, Zamorano: weed thicket
July 19, 1948, #106 (Hubbell), 3 males, 2 females: roadside, July
1, 1948, #10, 1 male, 2 females; vegetables, July 1, 1948, #13
(Hubbell), 1 male, 3 females; campus, Aug. 16, 1948, #224 (Hub-
1 For Part I of this series, see Pan-Pac. Ent., 26 (2): 86 - 90, 1950; for Part II,
see Jour. Washington Acad. Sci., 48 (2) :46-57, 1958,
248 | THE PAN-PACIFIC ENTOMOLOGIST [ VoL. xxx, No. 4
bell), 2 females; tall weeds, July 9, 1948, #45 (Hubbell), 2 males,
1 female; on gardenia, July 4, 1948, #25 (Hubbell), 1 female.
Tylos tabernilla (Cresson), 1926, Trans. Amer. Ent. Soc., 52,
p. 263 (Micropeza). Escuela Agricola, Zamorano: tall weeds, July
9, 1948, #15 (Hubbell), 1 female; weed thicket, July 19, 1948,
#106 (Hubbell) 1 female.
Tylos (Neriocephalus) sufflavus James, new species
This species traces to paragraph 42 or 45 in Hennig’s (1936,
p. 140) key (the first posterior cell being either closed in the costa
or short-petiolate) but will not run satisfactorily beyond those
points. The pleura are entirely yellow, at most discolored with
yellowish brown but without clearly-marked patches of that color,
and contrasting with the black mesonotum; all femora are yellow,
at most with their apices slightly discolored; the claspers of the
male are exceptionally large; and the ovipositor in the female is
exceptionally broadened and angulate apically on the non-retractile
portion, being as broad there as the greatest width of the abdominal
lerga.
Male.—Head moderately elongated, about 0.75 as high as long, the
eyes equal in length and height. Vertex and upper half of occiput, including
orbits, shining black; front between eyes orange-yellow, between posterior
margin of eyes and anterior ocellus reddish yellow, with an extension of this
area passing to each side of the ocellar triangle, first broadly, then narrowing
to a fine stripe that passes between the inner and outer verticals and termin-
ates on the occiput; front from eyes to bases of antennae reddish brown.
Face and lower part of occiput, except a small brownish area behind the
lower posterior corner of the eye, yellow. Pile of head very inconspicuous;
facial orbits silvery-tomentose. Inner vertical, outer vertical, and postvertical
bristles strong, black. Antenna reddish yellow; setulae of first and second
segments black; arista black, bare. Proboscis and palpi yellow. Mesonotum
including scutellum, and metanotum, black, at most slightly reddish along the
notopleural suture and on the postalar regions, subshining, dulled by a
cinereous pollen which becomes more or less brownish laterally. Prothorax
mostly yellow, pronotum and humeri reddish brown. Pleura yellow, at most
with areas on the mesopleura and pteropleura reddish brown. Upper parts
of pleura shining, the lower parts, especially of the sternopleura, whitish-
pollinose. Two strong notopleurals, 1 sternopleural, and several bristles on
the lower parts of the sternopleura before the middle coxae, black. Scutellars
strong, black. Wing slightly brownish-hyaline; apical cell closed in the
margin or short-petiolate; costal section between R23 and Rais less than half
the length of Miz (ratio about 30 to 65 or 70). Halteres yellow, knobs
brownish. Coxae yellow with black setulae and bristles; femora and tibiae
reddish yellow, without any trace of annuli but with the tibiae becoming
brownish at the apices, the fore pair sometimes mostly brownish; tarsi
OctToser, 1954] JAMES—TYLIDAE 249
brownish, the terminal tarsomeres somewhat enlarged. Abdominal terga I
to VI black with narrow lateral margins on all segments and broader, com-
plete apical margins on II to VI, sometimes becoming obscure on IV and
V; pollen as on the mesonotum. Epandrium dorsally and extremities of
surstyli reddish yellow, the ventral areas, including the sternites and the
copulatory claspers, yellow. Claspers large, almost as long as the first three
terga combined, ovate, broadest at three-fifths their length, from the lateral
aspect angulate apically, from the ventral (anterior) aspect incised, V-shaped,
to almost one-third distance from the apex; surstyli cruciate, the right
overlying the left, each with a broadly acute apex. Length, 8-9 mm.
Female.—Similar to the male, except sexually. Apical tarsomeres not
enlarged. Basal (non-retractile) part of ovipositor reddish-brown dorsally,
narrowed at base to apical width of sixth tergum, then becoming broader to
its apex and definitely angular at its outer corners; the retracile part yellow-
ish and narrowing strongly but gradually to the subcylindrical, blackish
apical portion. Comparative measurements (30=1 mm.): non-retractile part
of ovipositor, base 23, apex 33, length 20-25; basal width of subcylindrical
terminal part, 8; maximum width of abdomen (apex of tergum III), 33; apex
of tergum VI, 23.
Fig. 1. Tylos sufflavus, new species. Abdomen of male, lateral view, left
side, from a paratype. RS, right surstylus; LS, left surstylus.
Holotype male, Mt. Tancituro, MicHoacan, Mexico, 7800 ft.,
sweeping in mountain meadow (H. Hoogstraal), Fourth Hoog-
straal Mexican Biological Expedition, 1941. Allotype, same data
but on lupine, mountain meadow (Mt. Tancituro?). Paratypes, 4
males, 8 females, same data as holotype and allotype. Holotype
and allotype in the Chicago Natural History Museum.
I have seen a pair of specimens in the collection of the Chicago
250 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
Natural History Museum from Mt. Tancituro, in field, Fourth
Hoogstraal Mexican Biological Collection, which may be T pec-
toralis (Wiedemann) (=T. occipitalis Van der Wulp, according to
Hennig and Aczél). These specimens are smaller (6 mm.), the
mesopleura and pteropleura are marked with definite reddish
brown patches, the occiput is more broadly black in the middle,
the basal part of the ovipositor is almost parallel-sided and black-
ish dorsally, and the epandrium is marked with black dorsally.
The male genitalia are essentially as in sufflavus. If my identifica-
tion of pectoralis is correct, this species is very close to sufflavus.
Both Wiedemann’s and Van der Wulp’s species were described
from females only.
Oncopsia flavifrons (Bigot), 1886, Ann. Soc. Ent. France, (6)
6, p. 372 (Nerius). Tela: Lancetilla, July 28, 1948 (Hubbell), 2
females.
Glyphidops filosus (Fabricius), 1805, Systema Antliatarum,
p. 265. (Nerius). Tela: Lancetilla, July 28, 1948 (Hubbell), 1
female.
LITERATURE CITED
Hennic, WILLI
1935-6. Revision der Tylidae (Dipt., Acalypt.). II. Teil: Die ausser-
amerikanischen Taeniapterinae, die Trepidariinae und Tylinae.
Allgemeines uber die Tylidae. Konowia, 14:68—92, 192-216, 289-
310, 1935; 15:129-144, 201-230, 1936.
FIRST REPORT OF TRICHOCORIXA CALVA (SAY) FROM
MEXICO
(Hemiptera : Corixidae )
A single, male corixid, kindly identified by Dr. R. I. Sailer as
Trichocorixa calva (Say), was taken from a small, roadside pond
three miles north of El Mayor, Baja California, Mexico, October
6, 1953, by R. D. Lee, R. E. Ryckman, and C. T. Ames. Sailer’
noted previous collections from 27 states and the District of Colum-
bia in the United States, but it is believed that this is the first
record for the collection of T. calva in Mexico. The specimen is
now in the collection of the California Academy of Sciences.—
Rosert D. Lee, School of Tropical and Preventive Medicine, Loma
Linda, California.
1Sailer, R. I., 1948. The genus Trichocorixa (Coreidae, Hemiptera). Univ.
Kansas Sci. Bull. 32: 289-407,
OcrosBer, 1954] BERGAMIN—H YDROPONICS 251
UTILIZATION OF HYDROPONICS IN ECOLOGICAL
STUDIES OF THE COTTON APHID
J. BERGAMIN
Professor of Entomology, School of Agronomy,
University of Sao Paulo, Brazil."
The possibility of utilizing hydroponics in the investigations
of sucking insects offers a great deal of promise. The present writer
used this method in Brazil to excellent advantage during 1950 and
1951 in conducting a study of the coffee soft green scale, Coccus
viridis (Green). The growing of host plants in nutrient solutions
can be easily conducted in the laboratory, and has several ad-
vantages over growing plants in pots. The principal one is that it
is possible to remove the plants for short periods of time from the
nutrient solution in order to examine insect activity under a
binocular microscope.
Isily (1946) in studying the influence of nitrogen and pot-
assium on the behavior of the cotton aphid used nutrient solutions
to irrigate plants growing in sand. The same method was used by
Barker and Tauber (1951) in their study of the effect of nutritional
changes on the development of the green peach aphid, Myzus
persicae (Sulz.) and the pea aphid, Macrosiphum pisi (Kalt.).
Hydroponics has been used by Metcalf and Carlson (1950), David
(1951) and Metcalf and March (1952) in investigations involving
systemic insecticides.
In the present study, the cotton or melon aphid, Aphis gossypii
Glover was selected because of its great economic importance in
Brazil, the author’s homeland. Although a number of crops are
seriously injured, it is most destructive to cotton. The latter may
be heavily attacked during any stage of growth. Seedling stands
are frequently completely destroyed, and older plants may be
deformed, covered with honeydew and blackened with the growth
of the sooty mold fungus.
EXPERIMENTAL METHODS
The nutrient solution used was obtained from Hoagland and
Arnon (1950) and its composition was as follows:
1 Investigation was conducted at the University of California, Berkeley, under a
Fellowship granted by the Rockefeller Foundation.
5) THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
M1 used per liter to make
Stock Solution nutrient solution
1 M. potassium acid phosphate, KH:PO, . . ... =. 1
1 M. potassium nitrate, KNO; . . ..... =... 9
Vieeealeiam nitrate, =CaCNOn)s ta %ue Pe en ee al
1 M. magnesium sulfate, MgSO, . .. . Mir. Na meh
To furnish the needed micro elements 1] ml ni the following stock
solution was added to the above nutrient solution.
Grams dissolved in 1 liter
Chemical Compound of stock solution
bane ACh ce eh Pn Le ca Monks Sea! oe BG
manganese chloride, MnCl..4H:-O . . .... =... #181
Ane sultateriZnSO if hLO™ Lo «wae, aren aah (022
copper sulfates GuSOpsHsO. ows) aoe.) won Ue a ee ONS
molybdic acid, H:MoO.H:O
(assaying 85% MoO, PM ight | ete esth ee, ye Ue
Depending upon the size of plants desired, glass containers
ranging in size from 2 ounces to 14 gallon were used. In order to
discourage the growth of algae, the outside of the containers was
painted black, and then wrapped in paper or painted white or
aluminum to reflect heat.
The nutrient solutions were changed periodically because ac-
cording to Hoagland and Arnon (1950) plants “‘absorb the nutrient
salts, thus causing the acidity of the solution to change.” Although
there are methods for correcting the acidity, the above authors
stated that the situation can be taken care of by changing the solu-
tions every week or two.
Although plants grow best where the nutrient solution is con-
tinuously aerated, it was found in the present experiments that
satisfactory growth was obtained by aerating the cultures once a
day with a syringe. However, one experiment was conducted in
a greenhouse where continuous aeration was used,
Many kinds of plants were used. These included cucumber,
Crenshaw melon, honeydew melon, cantaloupe, pumpkin, squash,
and cotton. Although all of them grew well, squash appeared to
be the best suited for the present investigation.
Seeds were germinated in sand or sawdust, and the same day
they germinated they were transferred to the nutrient solution.:The
seedlings were passed through holes in the cork stoppers and
held in place with cotton packing. The plants were ready for use
OcroseEr, 1954] BERGAMIN—HYDROPONICS 253
as soon as the cotyledons reached a size where they could be
utilized. ;
Cages for rearing were 10 mm. in height and from 15 to 20 mm.
in diameter and were made of clear transparent plastic or glass
tubing. They were covered with cheesecloth or with either 40 or
60 gauge nylon, which was cemented on with Duco cement. The
cells were placed on the upper surface of the leaves with a thin
Fig. 1, Diagram illustrating means of holding cage in place on leaf.
board on the under surface and held in position with a rubber band
as shown in figure 1. The transparent wall of the cage made it
possible to observe aphid activity within the cell and after this
was done the cage could be removed and the young or the exuvia
could be brushed aside with a camel’s-hair brush, if such a pro-
cedure was desirable or necessary.
The investigation was conducted in a laboratory in which the
254, TIE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
temperature ranged from 70 to 80° F. Some rearing was also done
out of doors during the months of December, January, and Feb-
ruary where the mean temperature for December was 49.8, for
January 53.1, and February 53.2. A single experiment was con-
ducted in a greenhouse where the temperature ranged from 75
to 80° F.
Lire History STUDIES
Length of nymphal period: As soon as the nymphs are born
they begin to feed and continue to do so until their development is
complete. Twenty-five individuals were reared under laboratory
conditions and it was found that the nymphal period ranged from
© to 7 days with an average of 6.2 days. Ten individuals were
reared out of doors under December conditions. Here the range
was 15 to 24 days with an average of 17.3 days.
Number of instars: The number of instars under laboratory
conditions was studied in 25 wingless and 13 winged individuals.
In all cases the wingless individuals moulted 4 times while those
with wings moulted 5 times. The number of antennal segments
found in the several instars of the wingless form was 4 for the
first, 5 in the second and third, 6 in the fourth and 6 in the adult.
With the winged form the same condition was encountered and
there were 6 segments in the fifth instar and 6 in the adult. Under
laboratory conditions moults occurred in from 36 to 40 hours re-
gardless of the instar. Under December out-of-doors conditions the
period between moults was 4 to 6 days.
It is difficult to distinguish winged forms during the early in-
stars. Wing pads do not make their appearance until after the third
moult, so it is not until the 4th instar that winged and wingless in-
dividuals can be easily separated from one another.
Number of Progeny and Longevity of Adult Females: The
number of progeny and the length of adult female life was deter-
mined for out-of-doors conditions and in a greenhouse. In all cases
the females were caged separately and the rate of reproduction
observed. Each day the cultures were examined and the young
removed. A summary of the results obtained is given in table 1.
The length of life and the number of progeny produced was
greater under greenhouse conditions than out-of-doors. This is not
surprising because it is very possible that the winter temperatures
prevailing out-of-doors during the months of December, January
OcToBER, 1954] BERGAMIN—H YDROPONICS 255
and February were much below the optimum for this insect. The
results would certainly indicate that this was the case.
The reproductive potential of the females was greatest during
the first 10 days. The average number of young produced per
female per day under greenhouse conditions was 4.3 as compared
to 2.5 over the entire life. Similar figures for out-of-doors were
2.8 and 2.3.
An experiment was conducted out-of-doors to determine what
the total production from a single female might be. In 31 days
there were 249 progeny and in 42 days the population had
increased to 1,356 individuals. It is believed that under more fav-
orable temperature conditions a much larger population would be
encountered,
The reproduction was only by parthenogenesis and no males
appeared during the observations.
Production of Winged Forms: The natural factors that stimulate
the production of winged forms are not fully known. It is believed
by some that the production of winged aphids is a response to
increased population density. It is a means that insures survival
and dispersal of species. If only wingless individuals were produced
indefinitely the population would finally reach a point where the
plant would be killed, and the aphid population would die for
want of food.
Table 1. Length of adult life and the number of female progeny
produced out-of-doors and under greenhouse conditions.
Naomber Length of life Number of
Location of in days POS ENY.
individuals |
range average range | average
out of
doors’ 25 10—29 17.6 21-58 41.0
greenhouse 16 16-29 23.8 36—98 59.9
1 Months of December, January and February.
The production of winged forms may also be brought about
by physiological changes in the host which result from heavy feed-
ing by aphids. This has been suggested as a possibility by Goff and
Tissot (1932). The growing of plants in nutrient solutions should
256 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
aid in determining whether heavy aphid infestations tend to cause
physiological changes in the host plants.
As pointed out by Wigglesworth (1950) there are many ex-
ternal factors that influence the production of winged forms. These
include the lack of water, proteins and similar substances.
SUMMMARY
Hydroponics were successfully used to grow squash plants
upon which ecological studies of the cotton or melon aphid were
conducted. Under laboratory conditions (70 to 80° F.) the length
of the nymphal period ranged from 5 to 7 days with an average of
6.2 days. Out-of-doors under winter conditions the range was 15
to 24 days with an average of 17.3 days.
It was found that wingless individuals moulted 4 times while
those with wings cast their skins 5 times. Wing pads do not make
their appearance until after the third moult.
Under greenhouse conditions (75 to 80° F.) the length of adult
life averaged 23.8 days, while for winter conditions out-of-doors it
was only 17.6 days. The average number of progeny produced
under greenhouse conditions was 59.9 while for out-of-doors it
was 41.0
Factors that result in the production of winged forms are
discussed.
ACKNOWLEDGEMENTS
Thanks are due to Dr. E. G. Linsley, Chairman, and Dr. A. E.
Michelbacher of the Department of Entomology and Parasitology,
University of California; and to Dr. E. Malavolta, Associate Pro-
fessor in the School of Agronomy, University of Sao Paulo, Brazil,
and Associate Fellow in the Department of Plant Nutrition, Uni-
versity of California, for help and suggestions received.
LITERATURE
Barker, J. S. and O. E. TAUBER
1951. Fecundity of and Plant Injury by the Pea Aphid as Influenced by
Nutritional Changes in Garden Pea. Jour. Econ. Ent. 44(6):
1010-1012.
Davin, W. A. L.
1951. Insecticidal Action Studies with Bisdimethylaminophosphorous
anydre Containing Phosphorous. Ann. App. Biol. 38:508—-524.
Gorr, C. C. and A. N. Tissot
1932. The Melon Aphid. Aphis gossypii Glover. Fla. Agr. Exp. Sta.
Bull. 252, 1-23.
OcrosBeEr, 1954] BREAKEY—PITTOSPORUM SCALE 250
Hoacuanp, D. R. and D. I. Arnon
1950. The Water Culture Method for Growing Plants Without Soil.
Calif. Agric. Exp. Sta. Cir. 347:1-32.
Istiy, D.
1946. The Cotton Aphid. Ark. Agr. Exp. Sta. Bull. 462, 29 pp., 3 graphs,
37 refs.
Merca.r, R. L. and R. B. CARLSon
1950. Systemic Pest Conltrol Citrus Leaves. 30(9) :12, 13, 16.
Merca.r, R. L. and R. B. Marcu
1952. Behavior of Octamethyl Pyrophosphoramide in Citrus Plants.
Jour. Econ. Ent. 45 (6) :988—997,
WiccLesworTH, V. B.
1950. The Principles of Insect Physiology, 4th Edition, 544 pp., London,
Methuen & Co. Ltd., New York, E. P. Dutton & Co. Inc., Editors,
1950.
PIT-MAKING PITTOSPORUM SCALE IN WESTERN
WASHINGTON
(Homoptera :Coccidae)
E. P. BREAKEY
Washington Agricultural Experiment Stations,
Western Washington Experiment Station, Puyallup
On June 19, 1953, Mr. Sidney Walsh, Landscape Engineer for
the Washington State Department of Highways, left some samples
of broom at the Western Washington Experiment Station which
were infested with a scale insect. Mr. Walsh reported that this scale
insect was killing the broom in great quantities where it had been
planted to hold the banks of cuts made for U.S. Highway 99, below
Fort Lewis. The broom most severely damaged was known as
Genistus (Cytisus) kewensis. The plants were 10 to 15 years old.
These specimens were sent to Mr. C. F. W. Muesebeck, in charge
of the Division of Insect Detection and Identification, Bureau of
Entomology and Plant Quarantine, Washington, D. C., with the
request that the scale insect be identified. A letter dated July 13,
1953, reports that Miss Louise M. Russell had identified the scale
insect as Asterolecanium arabidis (Signoret), and the Division
of Cereal and Forage Insect Investigations had been notified for
possible further attention. |
The pit-making pittosporum scale has been a problem in Cali-
fornia for some time. According to Essig (1945), the insect is
widely distributed in Europe and in the northeastern part of the
United States. It is regarded with considerable concern in Cali-
258 THE PAN-PACIFIC ENTOMOLOGIST [ VoL. xxx, No. 4
fornia and elswhere because of its serious injuries to many valuable
ornamental plants, its rapid adaptation to an ever increasing
number of unrelated plants, and its correspondingly widening
distribtution.
Like many others, this scale appears to inject a toxin into the
host plant which causes cessation of growth, and on many plants
distorted, somewhat enlarged and often dead terminals of the
branches (Fig. 1)
EXPLANATION OF PLATE
Fig. 1, Genistus (Cytisus) kewensis infested with the pit-making pittos-
porum scale. Note distortions.
An examination of the brooms planted by the Highway De-
partment to hold the sandy banks of the cuts made for U.S. High-
way 99 on either side of the Nisqually River showed that the
variety Genistus (Cytisus) kewensis is the most severely infested
and injured. Another horticultural variety of broom is also being
injured and killed. However, Scotch broom which has escaped and
estblished itself among the infested plants on these same embank-
ments appears to be free of infestation at this time.
Essic, E. O. LITERATURE CITED
1945. The Pit-Making Pittosporum Scale. Bulletin, California Depart-
ment of Agriculture, 34(3) :134—-136.
OcrosBer, 1954] KROMBEIN—PERISIEROLA 259
A NEW PERISIEROLA FROM CALIFORNIA
(Hymenoptera: Bethylidae)
KarL V. KROMBEIN
Entomology Research Branch, Agricultural Research Service.
United States Department of Agriculture, Washington, D. C.
The present species is described at this time so that a name
will be available for use by W. H. Wade in his study of the para-
sites of the larvae of the phycitid moth, Myelois venipars Dyar,
the navel orangeworm. ;
_Perisierola breviceps Krombein, new species
Female—Length 3.4. mm., forewing 2.2 mm. Black; apex of
scape, pedicel, first flagellar segment, tibiae, and tarsi testaceous.
Wings clear hyaline; stigma and prostigma dark brown; veins very
pale yellowish.
Head scarcely longer than broad, poorly developed behind eyes; dis-
tance from posterior margin of head to posterior margin of eyes one-fourth
the eye length; clypeus with a strong, arcuate median keel, which extends
back on front a short distance beyond antennal insertions; dorsum of head
moderately coriaceous and with some scattered punctures; ocelli in a broad
triangle, the ocellocular line 1.5 as long as postocellar line; antennae ex-
tending back to posterior margin of pronotum. Thorax slightly narrower than
head; pronotum delicately coriaceous and with a few scattered, small
punctures, about 1.5 times as long as scutum; scutum with similar sculpture,
a little more than twice as broad as long, the notaulices present though
feebly impressed; scutellum about as long as scutum, separated from it by
an impressed groove, and feebly coriaceous; dorsum of propodeum strongly
coriaceous except for a narrow, slightly elevated, polished strip down middle,
the lateral margins strongly carinate, the posterior margin more delicately
so, the carina evanescent in middle; posterior surface of propodeum abruptly
declivous, flat, and delicately coriaceous; side of pronotum with moderately
close, parallel, oblique, fine carinae; mesopleuron delicately coriaceous; side
of propodeum strongly coriaceous. Abdomen somewhat broader than thorax,
as long as head and thorax combined, highly polished. Stigma longer than
broad; radius a little over twice as long as stigma, moderately curved;
median cell with only one or two microtrichiae.
Male. Unknown.
Holotype female, Tracy, SAN Joaquin County, CALIFORNIA,
April 29, 1953 (W. H. Wade; reared from Myelois venipars Dyar)
[U. S. National Museum, Type No. 62241]. Paratypes. 2 99; same
data as type [California Insect Survey, University of California,
Berkeley]. 1 2; same data as type, but July 25, 1953 [U. S. Na-
260 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
tional Museum]. The paratypes vary in length from 2.8 to 3.6 mm.,
and do not differ in any important details of the sculpture.
P. breviceps females are distinguished from those of the other |
described North American species by the following combination
of characters: the strong, arcuate clypeal keel; head poorly de-
veloped behind eyes; very broad ocellar triangle; and the almost
total absence of microtrichiae in the median cell.
INSECTS IN GRAIN, ELEVATORS AT PULLMAN AND
ALBION, WASHINGTON?
Yune-CuHanc CHao
Department of Entomology, State College of Washington,
Pullman, Washington
The twenty-six species of insects given in Table ]1 were recorded
from three grain elevators at Pullman and Albion, Washington,
during the time that experiments on residual sprays were being
conducted. Most of these species were taken from the floor samples
in empty treated bins. A few were obtained from damp, spilled
wheat below the bins. .
The granary weevil, the two species of flat grain beetles, the
saw-toothed grain beetle and the red flour beetle were most
abundant and economically important. Of the 9830 insects re-
covered, the percentages of these particular insects were 40.5, 26,
22.4, and 11.1 respectively. Microgramme filiformis and Lathridius
minutus are recorded for the first time from granaries in the United
States, although they have been reported from other stored food
products in several states. Microgramme filiformis, Trogoderma
simplex and Alphitophagus bifaciatus are all new Washington
records.” Trogoderma boron, recently described as new by Beal’
is the first record of this species’ occurrence in elevators from
Washington.
Other noteworthy finding are concerned with two species each
of Trogoderma, Tribolium, and Laemophloeus. Trogoderma simp-
WP iawerk conducted under Project No. 1127.
2 Personal communications from R. S. Beal, Melville H. Hatch, and Luella M.
Walkley.
3 Beal, R. S., 1954, Biology and taxonomy of the Nearctic es of Trogoderma.
Univ. of Calif. Publ. Ent., 10(2) :35-102, 18 figs.
Table 1. Insects in Grain Elevators at Pullman and Albion,
Washington, 1952.
OcrosBer, 1954] CHAO—GRAIN ELEVATOR INSECTS 261
COMMON NAME SCIENTIFIC NAME FREQUENCY
COLEOPTERA
Curculionidae
Granary weevil.......................-2--.--- Sitophilus granarius -.............--0----0------- often
Tenebrionidae ;
Red flour beetle.............2..20.2....222.--.- Triboltum castaneum: 20-0202. often
Confused flour beetle... Tribolium confUusum ...........-..---200-----0-000+ rare
Yellow meal worm.................------- Tenebrio molitor .....2..22.....2.000-00--000--- common
Gynaeus angustis eet 8 ee ee rare
Cucujidae
Flat grain beetle... Laemophloeus pusillus ..........0....202.-2------ often
Flat grain beetle... Laemophloeus turcicus ..........20--.2.---------- often
Saw-toothed grain beetle................ Oryzaephilus surinamensis ..............----- often
Foreign grain beetle........0.....0........ Ahasverus advena ......2...2..00.220000200-0-- very rare
Ostomidae
Cadelle.......... Tete Me ea: OS Tenebroides mauritanicus ............occasional
Ptinidae
White marked spider beetle........... EURAUUS TILT A rem isa ort tre Aes Me Nee) tad rare
Dermestidae
Trogoderma simplex. ............2..2000000--- common
Black carpet beetle... 2. AWMABENUS! DICEUS. ...c5. 2 i. cei see common
Trogoderma boron ............--.2.----+---- occasional
Larder beetle:..../..0. 020. nk Dermestes lardarius ........2...:11000020000200-0- rare
Chrysomelidae
Two-banded fungus beetle............. Alphitophagus bifasciatus ........20.20..-.20...-- rare
Lathridiidae
Microgramme filiformis. ................ occasional
Lathridius minutus ............-2..0..-.-.--- occasional
Mycetophagidae
Mycetophagus quadriguttatus...............--. rare
Cryptophagidae
Cryptopiagus spre lec. es rare
Cryptophagus spi 2.23 a rare
Gry PLO phRagUs |SPi Bo terse rare
LEPIDOPTERA
Pyralidae
Miealiinoghist is. 2y2 a iiocr any abs 5 yh alis Farinas. oes soit te ead. common
Tineidae
European grain moth...................... Nemapogon granella .............2020.000--- common
DIPTERA
Omphralidae
Window pane fly... eee Omphrale fenestralis .......ccscsesecccecceoeoeds rare
ACARINA
Laelaptidae
Grain mite.i 2. ..cecssceelesecles
uh a Haemolaelaps megaventralis ...........common
262 THE PAN-PACIFIC ENTOMOLOGIST [ VoL. xxx, No. 4
lex appears more frequently and abundantly than T. boron. In one
elevator at Pullman, this species outnumbered any other insect.
In seven bins of this elevator, it varied from 17 to 352, with an
average of 116. This insect is also among the five insects re-
covered from wheat samples for the study of field infestations
(Chao and others, 1953). It might be one of the most important
secondary insects in elevators in this area. Tribolium castaneum
was much more abundant than T. confusum. However, the reverse
should be true according to Good (1936). The two species of
Laemophloeus occur in similar numbers.
Luella M. Walkley identified Lathridius minutus and Micro-
gramme filiformis, and supplied the information on their habitats;
H. W. Capps identified Pyralis farinalis and E. W. Baker, Hamol-
aelaps megaventralis. The identifications of these species were made
through the courtesy of C. F. W. Muesebeck. R. S. Beal identified
the two species of Trogoderma and supplied the information on
their distribution. Melville H. Hatch identified Laemophloeus tur-
cicus and Mycetophagus quadriguttatus and supplied the informa-
tion on the distribution of Alphitophagus bifaciatus. Maurice T.
James identified Omphrale fenestralis. H. S. Telford assisted in
preparing the manuscript.
To all the men mentioned above, the writer is grateful.
REFERENCES CITED
CHao, YuNc-CHane, H. G. Stimxover, H. S. TELForp, and PETE STALLCOP
1953. Field infestations of stored grain insects in eastern Washington.
Jour. Econ. Ent. 46 (5) 905—907.
Goon, N. E.
1936. The flour beetles of the genus Tribolium. U. S. Dept. Agric. Tech.
Bull. 498 pp. 15-16.
BOOK NOTICE
THE GRASSHOPPERS AND LOCUSTS (ACRIDOIDEA) OF AUS.
TRALIA. Volume 2: Family Acrididae (Subfamily Pyrgomorphinae).
By James A. G. Rehn. Melbourne, July 1953. 270 pp., 32 pls. Price £ 2,
plus 3/10 postage. (Order from Tait Book Co., Pty. Ltd., 349 Collins
St., Melbourne, Vic., Australia. )
The first volume of this series was noted in the January, 1953 Pan-Pacific
Entomologist; the second is of similar format. The descriptions are full, those
of higher categories having much on probable phylogenies. Most of the
less known place names are documented iin footnotes. The photographs of
specimens are remarkably good, and very well reproduced. There are two.
new generic, three subgeneric, 15 specific and six subspecific names proposed.
—Hucn B. Leecn.
Ocroser, 1954] LINSLEY, et al—EXOMALOPSIS 263
A NOTE ON THE NESTING HABITS OF EXOMALOPSIS
SOLANI COCKERELL
(Hymenoptera, Anthophoridae)’ _
E. G. Linstey, J. W. MacSwain and Ray F. SmitH
University of California, Berkeley, California
The tribe Exomalopsini is of particular interest to students of
bees because of an apparently close morphological relationship to
to parasitic bees of the Nomadini. Two genera occur in the United
States, Exomalopsis and Ancyloscelis, but with the exception of an
observation by Hicks (1936) apparently the nesting habits of our
species have not been described. Hicks reported as follows: “Some
notes on the habits of the rare bee, Exomalopsis torticornis Ckll.
(det. Cockerell), were taken on June 24, 1926 at Los Angeles,
California. Four pollen laden females were seen, within a few min-
uts, entering a common nest entrance into the ground. Each came
out, in turn, after depositing the provisions and was caught at that
time. The nest was next dug out. The tunnel leading from the
entrance was in very dry and in exceedingly hard soil. These con-
ditions made it difficult to follow in digging, although I was able
to trace its course for a few. inches. It extended straight into the
earth for one inch, then turned to one side for one and one-half
inches where it again continued straight down for two inches. The
continuation at this point was lost but not until it had been
definitely shown that there was one tunnel and that all the bees
were using it. The nests may or may not have been separate. This
important point needs further investigation.”
Claude-Joseph (1926) found individuals of Exomalopsis caer-
ulea Friese in Chile using a common nest entrance but preparing
separate galleries. Each bee provisions a linear series of three to
six cells at an average depth of 20 cm. The jug-shaped cells are
smooth and varnished interiorly and are closed by a thick clay cap.
The egg is placed on top of the moistened pollen ball. The larva
consumes the pollen ball in about six weeks and over-winters in a
coriaceous cocoon.
During the second week of August, 1954, in an area nine miles
southwest of Fresnillo, Zacatecas, Mexico, where anthophorid bees
1 The observations reported here are part of a series of studies made possible by
a grant-in-aid from the Associates in Tropical Biogeography, University of Calfornia.
264 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No. 4
(Diadasia, Emphor, Melissodes, Anthophora, Tetralonia, and Hem-
isia) were nesting abundantly, a few females of Exomalopsis solani
Cockerell were observed taking pollen from flowers of Solanum
eleagnifolium Cav. Although this area was carefully searched and
bees intensely studied for a week, no Exomalopsis nesting sites were
discovered. One female was captured while entering an abandond
burrow of Emphor bombiformis (Cresson), but because of the
large diameter of the burrow the association was considered ac-
cidental and no particular signficance was attached to the observa-
tion. Later, however, another observation was made in connection
with a bee burrow which had been “pointed out” to us by a para-
sitic female of the genus Nomada (Micronomada) which clearly
indicated that it was a known host burrow. The Nomada was cap-
tured and two days later the burrow was excavated. The entrance
to this burrow was at the bottom of a shallow. cavity in the soil and
the shaft proceeded directly downward for fourteen and one-half
centimeters and then turned abruptly on the horizontal for three
centimeters. At the end of the burrow a worn female of Exomalopsis
solani was apparently digging. With the assistance of another
female Nomada a second nest of this type was located and deter-
mined to be that of Agapostemon texanus Cresson. Thus the Ex-
omalopsis had apparently appropriated an abandoned (or perhaps
active) Agapostemon. burrow.
Although our very limited observations can be regarded as
little more than suggestive, it does appear possible that Exomalop-
sis solani regularly appropriates abandoned (perhaps also active)
burrows of various genera of bees. If this proves to be true it
permits speculation as to the origin of a parasitic habit in this
group of bees which might have given rise to the related Nomadini.
Exomalopsis caerulea and E. torticornis are in different species
groups or subgenera from E. solani (Exomalopsis s. str.).
; LITERATURE CITED
Hicks, C. H.
1936. Nesting habits of certain western bees. Canadian Ent., 68:47—52.
CLAUDE-JOsEPH, F. .
1926. Recherches biologiques sur les Hyménoptéres du Chili. Ann. des
Sciences Naturelles, Zoologie, 9:113—268,
Ocroser, 1954]
Acarina, 119, 181, 261
Aceria tulipae, 87
Achaetoneaura archippivora, 186
Aeolothripidae, 209
Agapostemon, 264, texana, 264
Ahasverus advena, 261
Alloperla (Alloperla) chandleri,
179
Alphitophagus bifasciatus, 260,
261
Ameletus validus, 24
Ammonites mammillatus, 180
Amphizoa, 86
Andrena, 78
Andrognathidae, 221
Androlaelaps, 119, grandiculatus,
119
leviculus, 119
sinuosa, 119, 120
Aneristus ceroplastae, 8
Anicetus annulatus, 8
Anthocopa abjecta, 43
anthodyta bequaerti, 42
arizonensis, 43
elongata, 42
hebitis, 44
hemizoniae, 50
hurdiana, 47
hypostomalis, 49
mallognatha, 51
mirifica, 51
namatophila, 47
nigrior, 43
rubrella macswaini, 45
rubrella rubrior, 46
segregata, 48
Anthophora (Clisodon) furcata
syringae, 69
linsleyi, 69
Anthophoridae, 145, 203, 263
Ants, swarming of, 93
Apatolestes eiseni, 53
Aphaenogaster funkikoensis, 10
lepida, 10
phillipt menozzi, 10
Aphidae, 52, 251
Aphis pruni, 180
Apis mellifera, 70
Apoidea, 37, 68, 1383, 199, 203,
220, 263
Aradus evermanni, 90
Asteroleucanium arabidis, 257
Atrachelus cinereus, 158
Atractelmis, 125, wawona, 125
Attagenus piceus, 261
Augochlora pura, 67
Autographa californica, 186
Axobolus ergus, 226
Baetis alius, 32
INDEX TO VOLUME XXX
205
diablus, 30
leechi, 29
sulfurosus, 33
Bailey, Rhipidothrips, 209
Beal, Dearthrus, 231
Belkin, mosquito pupae, 227
Bergamin, Hydroponics & cotton
aphid, 251
Bethylidae, 259
Bibio, 180
Blaniulidae, 226
Blastothrix ozukiensis, 8
Blowflies, 147
Bombidae, 69, 220
Bombus americanorum, 69
caliginosus, 220
vosnesenskii, 69
Book notices, 34, 208, 234, 246,
262
Book reviews, 10, 14
Boudreaux, Tetranychid mites,
181
Brachycybe producta, 221
Brachydesmus (Brachydesmus)
yosemitensis, 224
Breakey, pittosporum scale, 257
Brown, Aphaenogaster lepida, 10
Buprestidae, 117
By-Laws, amendments to, 88
Californibolus pontis, 224
uncigerus, 224
Calliphora spp., 151
hominivorax, 150
Calliphoridae, 147, 150
Callitroga macellaria, 147
Calosoma semilaeve, 152
Camras, Zodion, 165
Canaceidae, 59
Canaceoides, 59
Cantharidae, 131
Capnia californica, 175
licina, 174
maculata, 174
oregona, 175
Carabidae, 152 .
Causey, millipeds, 221
Cerambycidae, 158
Ceratocombus, 85
Chandler, California dobsonflies,
105
Elmidae, 125
Chao, grain elevator insects, 260
Chapman, ant swarming on west-
ern U.S. mountain summits,
93
Chrysomelidae, 261
Cimicidae, 159
Cinara, 180
* New names in bold face, synonyms and homonyms in italics.
266
Coccidae, 257
Coccophagus sp., 8
hawailiensis, 8
ishii, 8
japonicus, 6
yoshidae, 6
Coccus pseudomagnoliarum, 5
Coenomyiidae, 137
Coleoptera, 11, 35, 117, 125, 131,
152, 158, 194, 195, 208, 231,
261
Colletes fulgidus, 67
Colobognatha, 221
Conopidae, 165
Corixidae, 250
Corydalidae, 70, 105
Cryptophagidae, 261
Cryptophagus spp., 261
Cryptostemma, 85
Ctenolepisma lineata, 73
rubro-violacea, 72
Cucujidae, 261
Curculionidae, 261
Cuterebra, 85
Cynaeus angustus, 261
Day, mayflies, 15, 29
Dearthrus, 231, longulus, 282
stebbinsi, 232
Denning, Lepidostoma, 187
Dermestes lardarius, 261
Dermestidae, 231, 261
Diabrotica undecimpunctata, 80
Diadasia enevata, 69
Diptera, 53, 59, 137, 147, 165,
227, 247, 261
Dobsonflies, 70, 105
Drosophila immigrans, 180
Dung beetles, collecting, 208
Dyslobus lecontei, 11
segnis, 11
Dysmicohermes crepusculus, 107
ingens, 105
Dysticheus rotundicollis, 12
Elmidae, 125
Emmesa testacea leeperi, 35
Emphor bombiformis, 69, 263
Endeodes, 195, basalis, 196, 197
blaisdelli, 196
collaris, 196, 198
insularis, 196, 198
rugiceps, 196
Eosentomon pallidum, 85
Epantus obscurus, 195
Ephemerella hystrix, 25
levis, 15
proserpina, 26
soquele, 18
spinosa, 25
yosemite, 26
Ephemeroptera, 15, 29
Erynnis lacustra, 85
THE PAN-PACIFIG ENTOMOLOGIST [ VOL. xxx, No. 4
Essig, Myzus langei, 52
Eucerceris flavocincta, 11
ruficeps, 11
superba, 11
Eucybe clarus, 221
Evans, Tastiotenia male, 103
Exomalopsis caerulea, 263
sidae, 145
solani, 263
torticornis, 263
Fender, Malthodes, 131
Formica spp., 97
Formica sanguinea subnuda, 97 .
Formicidae, 10, 93
Fossils, insect, 82
Furman, Androlaelaps, 119
Garner, reverse predation in Car-
abidae, 152
Gelastocoridae, 113
Glaresis ecostata, 82
Globicornis (Pseudomesalia)
kulti, 232
Glutops, 137, punctata, 138
rossi, 137
singularis, 139
Glyphidops flosus, 250
Gressitt, Flanders, and Bartlett,
parasites of citricola scale,
5
Haematosiphon inodorus, 159
Haemolaelaps megaventralis, 261
Halictus tripartitus, 68
Harpaphe haydeniana, 221
pottera, 222
Helfer, Hippomelas, 117
Hemiptera, 1, 112, 1138, 148, 153,
159, 161, 250
Hesperia uncas lasus, 84
Hippomelas dianae, 117
Hofmannophila pseudospretella,
220
Holonomada, 78
Homoptera, 5, 52, 251, 257
Hoplitis (Acrosmia) perissocera,
Hoplitis albifrons argentifrons,
39
biscutellae, 42
bullifacies, 37
grinnelli grinnelli, 39
grinnelli septentrionalis, 39
hypocrita, 39
laevibullata, 40
mazourka, 38
mesae, 43
producta interior, 39
rufina, 40
truncata mescalerium, 39
truncata truncata, 38
uvulalis, 39
Horen, tick collecting, 112
OctrosBer, 1954]
Hurd, Xylocopa californica, 199
Hussey, Pselliopus, 153
Hybaphe tersa, 222
Hydrellia griseola, var. scapul-
aris, 86
Hydroponics, 257
Hymenoptera, 11, 37, 63, 94, 108,
124, 133, 145, 146, 199, 208,
220, 2385, 259, 263
Hypoaspis, 220
Insects and mites, differences, 80
Ischnocybe plicata, 221
Isogenus (Kogotus) alameda,
178
Isoperla marmorata, 178
James, Tylidae, 247
Jensen, Potato psyllid, 161
Jewett, stoneflies, 167
Juloidea, 226
Krombein, Perisierola breviceps,
259
Lachnus, 180
Laelaptidae, 119, 220, 261
Laemophloeus pusillus, 261
turcicus, 261
Lasioglossum (Chloralictus)
sparsum, 67
Lasioglossum (Evylaeus)
kincaidii, 67
Lasioglossum (Sphecodogastra)
aberrans, 11
Lathridiidae, 261
Lathridius minutus, 261
Lecanium pseudomagnolarum, 5
Lee, phototropism in Mexican
chicken bug, 159
Trichovorixa calva, 250
Lepidoptera, 261
Lepidostoma, 187, astanea, 190
cantha, 193
cascadensis, 193
errigena, 188
frosti, 193
hoodi, 193
mira, 189
ontario, 193
podager, 193
quercina, 193
querla, 193
recina, 188
reosa, 192
roafi, 193
spicata, 190
strophis, 193
swannanoa, 193
tibialis, 192
togatum, 194
unicolor, 194
Lepismatidae, 56, 72
Leptidiella brevipennis, 158
INDEX TO VOLUME XXX 267
Leptophlebia invalida, 277
Leptothorax sp., 97
canadensis, 97
Leptotylus, 143
Leucolepisma, 74, arenaria, 74
se Leptidiella brevipennis,
1
Linquist, flies attracted to de-
composing liver, 147
Linsley & MacSwain, habits and
prey of Eucerceris ruficeps,
11
Linsley, MacSwain, & Smith, Ex-
omalopsis, 263
Lycandades purpurea crispa, 86
Lyceanea dispar batavus, 79
dispar dispar, 79
Macrosiphum pisi, 251
Maddux, dobsonfly, 70
Madremyia saundersii, 186
Malachiidae, 195
Malkin, Melandryidae, 35
Notonecta shooteri, 112
Malthodes stacesmithi, 131
columbiensis, 131
Mantispidae, 82
Megachile centuncularis, 146
Megachile (Chelostomoides), 68
Megachile (Litomegachile)
brevis, 68
Megachilidae, 37
Megaloptera, 70, 105
Melanargia, 180
Melandryidae, 35
Meloidae, classification, 91
Melecta armata, 69
miranda, 69
spp., 69
Melitoma, 82, 90
Metaphycus sp., 8
Michelbacher & Hurd, Monodon-
tomerus, 146
Michener, Hoplitis & Anthocopa,
Sie
bee pupae, 63
Microgramme filiformis, 260, 261
Micropezidae, 247
Microterys flavus, 8
okitsuensis, 6
Millipeds, 221
Miridae, 143
Mirolepisma deserticola silves-
tri, 56
Mitoura nelsoni muiri, 85
Moneilema gigas, 85
Monodontomerus montivagus,
146
Mononyx, 113
Moore, Eindeodes, 195
collecting dung beetles, 208
268 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. xxx, No.
Musca domestica, 151
Mycetophagidae, 261
Mycetophagus quadriguttatus,
261
Myrmecocystus semirufa, 57
Myrmecophila, 57
Myrmecophile, 56
Myrmica aldrichi, 97
lobicornis fracticornis, 97
rubra, 101
Myrmica (Myrmica) sp., 97
Myrmosa unicolor, 124
Myrmosula rutilans, 124
Myzus callangei, 52
langei, 52
persicae, 251
Nearctodesmidae, 223
Nearctodesmus olympus, 223
Nemapogon granella, 261
Nemotelus, 180
Nemoura spiniloba, 172
wahkeena, 171
Neopasites sp., 68
Nerthra fuscipes, 113
martini, 113
mexicana, 115
stygica, 115
usingeri, 116
Nocticanace, 59, arnaudi, 59
chilensis, 61
texensis, 62
Noctuidae, 152
Nomada, 78
Nomada (Gnathias) debilis, 135
opacella, 133
Nomada (Micronomada), 263
Nomadopsis anthidius, 203
euphorbiae, 67
scutellaris, 124
Nomenclature, zoological, 179
Nomia melandri, 68
Notonecta shooteri, 112
Notonectidae, 112
Oligotylus, 148
Omphrale fenestralis, 261
Omphralidae, 261
Oncopsia flavifrons, 250
Ophryastes sulcirostris, 11
Ophyra spp., 150
Optioservus canus, 130
Oreopasites vanduzeei, 203
larva of, 203
Oriulus medianus, 226
Oryzaephilus surinamensis, 261
Ostomidae, 261
Otobius megnini, 80
Pacific Coast Ent. Soc.,
Field trip, 83
Proceedings, 77
Palmatotriton, 180
Papilio machaon brittanicus, 79
Paraiulidae, 226
Paraleptophlebia cachea, 22
gregalis, 27
Paralucilia wheeleri, 151
Paratrioza california, 161
cockerelli, 161
Parshley, Howard Madison,
obituary, 1 :
Peltoperla (Sierraperla) cora,
170
Peltoperla (Soliperla) campan-
ula, 167
quadrispinula, 169
thyra, 167
Perisierola breviceps, 259
Peritelinus oregonus, 194
Pepsis, 77
Phaenicia spp., 147
Philip, North Amer. Tabanidae,
53
Philotes enoptes, 84
rita, 84
Phormia regina, 147
Phototropism, 159
Phyconomus marinus, 195
Pisonopsis, 235, anomala, 235
argentinus, 235
birkmanni, 235, 244
clypeata clypeata, 235, 240
clypeata occidentalis, 235, 242
triangularis californica, 235,
245
triangularis triangularis, 235,
Pitelka, use of bird nest by bum-
blebee, 220
Plecoptera, 167
Pogonomyrmex barbatus var.
nigrescens, 56
californicus, 57
californicus estebanius, 57
occidentalis occidentalis, 57
Policana herbsti, 67
Polydesmidae, 223
Polydesmoidea, 221
Pompilidae, 103
Protochauliodes aridus, 70
montivagus, 111
simplus, 110
Protura, 85
Psallus brevitylus, 144
Pselaptrichus, 85
Pselliopus cinctus, 158
karlenae, 153
latisfasciatus, 158
latispina, 156
zebra, 155
Psyllidae, 161
Ptinidae, 261
Ptinus fur, 261
Octoser, 1954]
Pupae, bees, 63
mosquito, 227
Pyralidae, 261
Pyralis farinalis, 261
Reduviidae, 153
Reticulitermes hesperus, 57
Rhagionidae, 139
Rhinigia cinctiventris, 158
Rhipidothrips, 209, brunneus, 210
cahirensis, 210, 212
cinctus, 210, 212
gratiosus, 210, 213
kellyanus, 210, 216
niveipennis, 210, 216
uzelianus, 217
Rhithrogena decora, 19
flavianula, 24
Rhizelmis, 126, nigra, 128
Rickera, 176, venusta, 176
Rosenstiel, strawberry weevil,
195
Ross, Book Review, 14
Roth, Book Review, 10
Rozen, Oreopasites larva, 203
Seale, citricola, 5
parasites of, 5
Scatopse, 180
Scytonotus amandus, 223
Sierraperla, 170
Sitona californicus, 12
Sitophilus granarius, 261
Slater & Knight, Oligotylus and
Leptotylus, 143
Snelling, Myrmosula rutilans,
124
Exomalopsis sidae, 145
Solenopsis, 57
Stator limbatus, 85
Stomoxys, 180
Sphecidae, 11, 235
Sphecophaga burra, 80
Spirobolidae, 224
Spiroboloidea, 224
Stentor, 180
Stratiomys, 180
Strophopoda, 143
Symphoromyia, 140, atripes, 141
fulvipes, 141
johnsoni, 141
kineaidi, 141
limata, 141
montana, 141
pachyceras, 141
plagens, 141
sackeni, 141
securifera, 141, 142
varicornis, 141
Synthesiomyia nudiseta, 151
Tabanidae, 53
INDEX TO VOLUME XXX
269
Taeniaptera lasciva, 247
latitibia, 247
Taiulus tiganus, 226
sp., 226
Tarantula, 77
Tastiotenia festiva, 103
Tenebrio molitor, 261
Tenebrionidae, 261
Tenebroides mauritanicus, 261
Tetranychus cocosinus, 261
magnoliae, 184
merganser, 181
Thermobia domestica, 57
Thysanoptera, 209
Thysanura, 56, 72
Tick collecting, 112
er ens Nomada (Gnathias)
13
Tineidae, 261
Tiphiidae, 124
Todd, Nerthra, 113
Tribolium castaneum, 261
confusum, 261
Trichocorixa calva, 250
Trigona cupira, 70
Trogoderma boron, 260, 261
granarium, 89
simplex, 260, 261
Tubaphe, 222, levii, 223
Tylidae, 247
Tylos abbreviatus, 247
tabernilla, 248
Tylos (Neriocephalus) stigmati-
cus, 247
sufflavus, 248
Usinger, Parshley obituary, 1
Utoiulus leechi, 226
utus, 226
Vermileo comstocki, 140
opacus, 139
Veromessor pergandei, 57
Vespula, 80, pennsylvanica, 80
Virus, transmission, 86
Vitula serratileneella, 80
Volucella, 180
Wall, Myrmecophile, 56
California Lepismatidae, 72
Wicken Fen, 78
Williams, Pisonopsis, 235
Wirth, intertidal flies, 59
Glutops, 137
Xylocopa californica californica,
200
californica arizonensis, 200
californica diamesa, 200, 202
virginica, 68
Xystodesmidae, 221
Zodion californica, 165
Zophina, 54
Zophotabanus, 53
Published by the
Pacific Coast Entomological Society
in cooperation with
The California Academy of Sciences
VOLUME THIRTY.
1954
EDITORIAL BOARD
P. D. HURD, JR., Editor
HUGH B. LEECH, Associate Editor
E. G. LINSLEY, Associate Editor
R. L. USINGER, Associate Editor
E. S. ROSS, Assistant Editor
R. C. Miller, Treasurer
A. E. MICHELBACHER, Advertising
PUBLICATION COMMITTEE
1954 1955 1956
E. L. Kessel E: R. Leach E. O. Essig, Chairman
H. B. Leech E. G. Linsley G. F. Ferris
San Francisc, California
1954
i
CONTENTS FOR VOLUME XXX
Bailey, Stanley F.
A review of the genus Rhipidothrips Uzel_................ 209
Beal, Jr., R.S.
Classification of the dermestid genus Dearthrus with
description of a new western species..............:-..-0-leeeeeee-e- 231
Belkin, John N.
The dorsal hairless setal ring of mosquito pupae.................. 227
Bergamin, J.
Utilization of hydroponics in ecological studies of the
COULOlmcIO MI Cemmcie et rhctea he sAolrored Sal WM ed ale sete dee 251
Boudreaux, H. Bruce
New. species of Tetranychid mites..............020.0.00000.2--e--- 181
Breakey, E. P.
Pit-making pittosporum scale in western Washington............ 257
Brown, Jr., W. L.
The synonymy of the ant Aphaenogaster lepida Wheeler.... 10
Camras, Sidney
A new species of Zodion from California......................-------- 165
Causey, Nell B.
New records and species of millipeds from the western
United States: and Canada ic eee bee 221
Chandler, Harry P.
Four new species of dobsonflies from California.................. 105
New genera and species of Elmidae (Coleoptera) from
(COfeT Wn Mos athe mG Wes eat saan ores 0 RON Lae near RS ea aa 125
Chao, Yung-Chang
Insects in grain elevators at Pullman and Albion,
Washington’ 222.0032) ioe TRACE Fee eller re OMY AIA DOONES: 260
Chapman, John A.
Swarming of ants on western United States mountain
SUIEMILS er eee ue ee es Toate ai lk ace He hl es Sait ee Fe Se Oa 93
Day, W. C.
New species and notes of California Mayflies IT.................... 15
New species of California Mayflies in the genus Baetis........ 29
Denning, D.G.
New species of Lepidostoma.........-.......-cse:-ceeeeceeeeeeeeeeeeseeeees 187
Essig, E. O.
Change of the species name of Myzus langei Essig to
My zusicallanver Pssigucy ii Meg SE el ee 52
il
Evans, Howard E.
The male of Tastiotenia festiva.................22220.0cc:2200cceeeeeneeeeees 103
Fender, Kenneth M.
On some Malthodés: sc). es RR 131
Furman, Deane P.
A new. species of Androlaelaps from Perognathus in
solbhern Galiornra sive 0 wd Saris Mime Mase Sh ees re. Al 119
Garner, William V.
A case of reverse predation in the Carabidae........................ 152
Gressitt, J. Linsley, Flanders, Stanley E., and Blair Bartlett
Parasites of citricola scale in Japan and their intro-
ddchon-=inte; Caliterata: 5)" iene eee 5
Helfer, Jacques R.
A new Hippomelas from California..................222...22..-2:0-2--+- 117
Horen, W. Peter
Modified flag for tick collecting................22.20...2----2etee ee dal?
Hurd, Jr., Paul D. |
A polytypic interpretation of the California carpenter
bee, Xylocopa californica with the description of a
new subspecies and notes‘on a possible polytopic form.......... 199
Hussey, Roland F’.
Two new species of Pselliopus and some distributional
TGCEShe 2 EP see ts Rate ac ote Rat Wen, Pes Ace 153
James, Maurice T.
The Diptera collected on the Cockerell and Hubbell
Expeditions to Honduras. Part III: Tylidae, with a
new ‘species trom Wlexico-.5. 7 7 ft 3s das eee 247
Jensen, D. D.
Notes on the potato psyllid, Paratrioza cockerelli (Sulc)....161
Jewett, Jr., Stanley G.
New stoneflies from California and Oregon.................-......--.- 167
Krombein, Karl V.
A new Perisierola from Califormia............02.00..-.cteccceceenee-e- 259
Lee Robert D.
The absence of negative phototropism in the Mexican
chicken bug, Haematosiphon inodorus (Duges).................. 159
First report of Trichocorixa calva (Say) from Mexico........ 250
Leech, H. B.
Book notice: A check list of the genera and species
of Mallophaga ..................... 34
FINO I REIS IIIS SN IOI III
?
iil
Leptidiella brevipennis (Mulsant) reared from Toyon.......... 158
Book notice: The coconut rhinocerous beetle (Oryctes
rhinoceros) with particular reference to the Palau Islands 208
Book notice: Fleas, flukes and cuckoos.................................-234
Book notice: The taxonomy, phases, and distribution
of the genera Chortoicetes and Austroicetes.....................-.. 246
Lindguist, Arthur W.
Flies attracted to decomposing liver in Lake County,
GUUS 20% g aUErE Mera SN ee aM Pt gi £ hye Cm eye ste ralen nS UAas eR 147
Linsley, E. G., and J. W. MacSwain
Observations on the habits and prey of Eucerceris
TUTE p shou emy. berth We) ee MOM lel eta oF Nee oak Sasseelt Me ieee: 11
Linsley, E. G., MacSwain, J. W., and Ray F. Smith
A note on the nesting habits of Exomalopsis solani
Gige eee ll etudarstt ote ira ae eet raat ier! Ved ciel eet Se 263
Maddux, Donald E.
A new species of dobsonfly from California.................2........ 70
Malkin, Borys
A new. northwestern melandryid................2-.2--22.-.2::e::e000000-- ao
Range of extension of Notonecta shooteri...................2...-2----- 112
Michener, Charles D.
Descriptions and records of North American Hoplitis
AIGA TENOCO Dae aie wie Wil eis rier ot Pd ayes Le 37
Observations on the pupae of bees.............2222.22222..2:2:eee0eeoe- 63
Michelbacher, A. E. and P. D. Hurd, Jr.
Monodontomerus montivagus Ashmead, a parasite of
Megachile centuncularis (Linnaeus) ..............2-20-2.--e-eee 146
Moore, Ian
Notes on Endeodes LeConte with a description of a
new species from Baja California.................22..222220.22.22.-2--+- 195
An efficient method of collecting dung beetles...................... 208
Pacific Coast Entomological Society
EEO GES CUTIE Yee tycee) at DEM we Ae eStats 77
eels thi psa cers ser cal ae Leite tes A To BAN i et NE 83
Philip, Cornelius B.
New North American Tabanidae (Diptera). Part IV:
Zophina new genus for “Apatolestes” eiseni Town-
send from Lower California. .....1......00......020.22200cseeesckeeeseedenes 53
Pitelka, Frank A.
Use of bird nest by bumble bee..........-.-.2-..2.2-..ee-. eee 220
iV
Slater, James A. and Harry H. Knight
The taxonomic status of Oligotylus Van Duzee and
Leptotylus Van Duzee with the description of a new
SOLE OF CaS (Celie ck b rae ase ia he at Ne PMSMAD ADEE RRO Ms ne EWA 143
Snelling, Roy R.
The host of Myrmosula rutilans (Blake) _..........2..20222..20..-.... 124
Records of Exomalopsis sidae in California and Baja
Balto R Mae S 2 RL pile. Fe ee! Ne RIN UE oe ee Pe 145
Rosenstiel, R. G.
Another weevil injurious to strawberries.....................----------- 194,
Ross, E. S.
Book Review: The ants of California............2.20222.0002---------- 14
Roth, Vincent D.
Book Review: How to know spiders............2...2..22:2::02002000-+- 10
Rozen, Jr., Jerome G.
Morphological description of the larva of Oreopasites
yvandugeel ‘Gockerelli, 0.000 ns etn a, eee Ae 203
Timberlake, P. H.
Two new species of Nomada, subgenus Gnathias, from
Galifonniar Sieh ic oe eee Se ae Be Pe athe iy 133
Todd, E. L.
New species of Nerthra from California...............2...2.2..2.--+--- 113
Usinger, Robert L.
Howard Madison Parshley...........2.202222222-.2.2-teeeeeeeeeeeeeeeeeees ]
Wall, Jr., William J.
Mirolepisma deserticola silvestri, a myrmecophile
ion Galt orate we kiln te ee rel be eS CRD i, See Cee 56
A redescribed species and a new genus and species of
the family Lepismatidae in California.........20222000000002022.---- 72
Williams, Francis X.
The wasps of the genus Pisonopsis..................----.--:00000-0+ Za
Wirth, Willis W.
A new intertidal fly from California, with notes on the
genus: Nocticanace Malloch... 0.00 99
A new species of Glutops and other new records of
GalitorniasTabanoidea -6229 Aim. Wet. Wi enh re oN 137
MAILING DATES FOR VOLUME XXX
No. 1 March 30, 1954. No. 3 September 30, 1954
No. 2 June 24, 1954. No. 4 November 18, 1954.
Announcing...
REVISION OF THE SPIDER MITE
FAMILY TETRANYCHIDAE
By A. Earl Pritchard and Edward W. Baker
This world-wide treatment (300 pp., 330 figs.) of the
“Red Spider” is the second volume in the Memoirs Series
of the Pacific Coast Entomological Society. Each species
is beautifully illustrated in the inimitable style of E. W.
Baker. The work deals with the systematics, identification,
and economics of the “Red Spiders”. Synoptic keys have
been prepared, descriptions are presented for all the
species including the major agriculture pests, and some
twenty species are described as new.
Publication date December, 1954
Special Prepublication Price: $9.00
Please place my order for..................- copy(ies) at the
special prepublication price of $9.00.
Sead prepublication orders to:
Treasurer, Pacific Coast Entomological Society
CALIFORNIA ACADEMY OF SCIENCES
Golden Gate Park 18, San Francisco
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