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DIPTERA
> BAM. BLEPHA ROCERI DE
By VERNON L. KELLOGG
1907
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48
DIPTERA
FAM. BLEPHAROCERIDÆ
DIPTERA
FAM. BLEPHAROCERIDÆ
by VERNON L. KELLOGG
WITH 2 PLAIN PLATES
HE flies belonging to the family Blepharoceridæ, or net-winged midges, have long been of
ety peculiar interest to entomologists because of the small number of known species and their
EN
supposed rarity, because of the wide and discontinuous distribution of these known
forms, because of the remarkable aquatic life of larvae and pupæ, and the strange
modification of the body in both these stages in conformity with the curious habits, and because of the
peculiar pseudo-net-veining of the wings of the imagines produced by a series of folds in the wing
membranes. The imagines also present a structural peculiarity of interest in the divided character of
the compound eyes. The eyes of these flies (as shown by the writer in 1900) are composed of ommatidia
of two types, differing in size, in amount of pigmentation, and to some extent in arrangement of the
retinal elements, and in their situation in the eye. These differences result in the possibility of a certain
degree of accommodation to different intensities of light.
The Blepharoceride were introduced as a family by Rondani (Prodr. Dift., Vol. 1, 1856) under
the name of Asfhenide, without any definition. In 1862 (Monogr. N. A. Dipt., Vol. 1, p. 6, 1862) the generic
name Z£Esthenia Westwood having to be given up as preoccupied, Loew gave the family name of Blepha-
roceridæ. « He had no other choice for the name », says Osten-Sacken, « because the genus Blepharicera
Macquart (or Blepharocera, as Loew amended it) was in 1862 the only published genus in the family. »
Liponeura Loew (1844) was at that time considered by Loew as a synonym of Blepharocera and the genus
Tanyrhina, from Ceylon, which he mentions at the same time with Blepharocera was merely a name
without description, Osten-Sacken, in 1895 (« Contr. to the Study of the Liponeuridæ », Berl. Ent.
Zeitschr., Vol. 40, p. 148-169, 1895), gave the name Liponeuridæ to the family, but in a supplement to
this paper (Berl. Ent. Zeitschr., Vol. 40, p. 351-355, 1895), and even previous to that (Ent. Monthly Mag.,
Vol. 31, p. 118, 1895), reestablished the name Blepharoceridæ. The first species descrided in the family
DIPTERA
was Blepharocera (Æsthenia) fasciata Westwood, described in 1842 from a specimen taken in Albania on
the Balkan peninsula. Macquart described the same species, in the Ann. Soc. Ent. Fr., 1843, from a
female specimen taken by Mr. Arnaud in 1841. The other few European species were discovered slowly,
one at a time, as were also the few South and Central American species, and the single species recorded
from Ceylon. In 1863 Osten-Sacken found the first North American species, Blepharoccra tenuipes. Since
that time the additional North American species have been found also slowly and one at a time until
1901, when four new species were discovered in one locality in California. There are known to-day
twenty species of these curious flies, well distributed over the world. There are certainly other species
to be found, but there are probably not many. The.flies are too conspicuous and characteristic long to
be overlooked in any locality visited by collectors. However, their favorite haunts are rather removed
from the more usual collecting grounds of entomologists. Special search will have to be made in
mountain regions, where clear, swift streams run over clean rock beds, if the still unknown living species
of the family are to be discovered.
Family Characters. — The flies are moderate-sized, elongate and bare, with long legs and
broad wings. These wings (pl. 2) contain no discal cell and have a peculiarly large and angular anal
lobe. In some species there is apparent a strong iridescence of the wing surfaces, although in others
these shifting colors are not so obvious. Alula, tegula and anti-tegula are absent or rudimentary. The
unique character is the presence of the « secondary venation », or the net of rather faint, fine crease-like
lines on the wings (pl. r, fig. 7; pl. 2, fig. 19). This net-like lining has nothing in common with the
primary or true venation, but is simply the result of the folding of the wings in the pupa. Because of the
curious habits of life (spoken of in the latter paragraph on the biology of the insects) the wings must
necessarily be fully developed at the moment that the imago issues from the pupa. But that these fully
developed wings may be accomodated underneath the pupal cuticle it is necessary that they be strongly
and repeatedly folded. The lines of these foldings constitute the so-called « secondary venation » charac-
teristic of the imaginal wings. The eyes are usually dichoptic in both sexes, but are occasionally
holyptic in one or both sexes. They are usually bi-sected by an unfaceted cross-band or line separating
each eye into two fields, an upper and lower one, the upper composed of larger and less pigmented
ommatidia (large and brown facets), the lower composed of smaller and more strongly pigmented
ommatidia (small black facets) (pl. 1, figs. 1, 2, 3, 4 and 12). In a few species the eyes are bi-sected only
in one sex. Three rather large ocelli are present. The antenne (pl. 2, figs. 16 and 17) are slender, with
from nine to fifteen segments clothed with a short pubescence. The mouth parts (pl. r, fig. 13) are
elongate, the females having in addition to labium and maxille, slender flattened elongate saw-like
mandibles; the males are without these mandibles. Both sexes have a slender elongate labrum-
epipharynx, a similarly slender elongate hypopharynx, a pair of slender blade-like maxillar with
five-segmented palpi, and labium with slender elongate basal sclerite and a pair of free, fleshy, terminal
lobes without pseudo-trachez and with no palpi. The thorax has a distinct, broadly interrupted, trans-
verse suture. The legs are moderately slender and comparatively long, the hind pair much longer than
the anterior ones, the front femora of the males curved in some species, the tibiæ with or without spurs,
the ungues generally somewhat incrassate at the base, sometimes beset with stiff, minute bristles on the
outside; the empodia very small, almost rudimentary, and the pulvilli wanting. The forceps of the
male (pl. 2, fig. 15) are somewhat like those in Limnobina, but are flatter, with various modifications;
the ovipositor of the females (pl. 2, fig. 14) is composed of two small, rather obtuse, lamella.
Biology and Habits, — The eggs and egg-laying of the Blepharoceride are yet unknown.
However, from the circumstances of the larval life it is nearly certain that the eggs are deposited on
sprayed or otherwise wetted stones just above the water in swift, clear mountain streams, or on wetted
FAM. BLEPHAROCERIDÆ 3
stones at the water’s edge. The larvæ and pupæ of one European species, one Brazilian species and one
North American species, are known. The larvæ of all Blepharoceridæ yet known live submerged in
swiftly running clear streams, which practically limits their occurence to mountainous, or at least, to
hilly regions. They are found usually in groups of lesser or greater number in favorable spots, some-
times, as in the case of Blepharocera tenuipes, in Coy Glen, near Ithaca, N. Y., forming « patches » of
hundreds of individuals clinging to the smooth rock bed of the stream, with from an inch to two inches
of water running swiftly over them. In Colorado and California the larvæ of Bibiocephala and of
Blepharocera have been found more scattered, and usually more deeply submerged; this is usually
caused, or at least the other condition made impossible, by the broken condition of the stream beds,
which are usually composed of separate stones of various sizes rather than of smooth bed rock. The
larve (pl. 1, f. 5, 6, 8 and 9) are curious, flattened, slug-like creatures, legless, but enabled to cling
firmly to the rock by means of six ventral suckers (whose structure and mode of use are described by
Kellogg, Proc. Calif. Acad. Science, ser. 3, vol. 3, p. 203, ff., 1903). When disturbed, the larvæ can hold
so fast to the rock that the body is more readily torn in two than dislodged as a whole. Locomotion,
which, though slow, is freely accomplished, is in a lateral direction; the moving larva loosens the hold
of three suckers at a time and swings to one side the hinder half of the body thus released, the suckers
again attach this part of the body in its new position, and the other half of the body is loosened and
swung over, and thus a slow lateral translation of the larva takes place.
The larva seem to feed chiefly on diatoms, although other food is doubtless taken. The older
larvee of Blepharocera tenuipes (New York) almost always bear a dorsal, felt-like covering, which is com-
posed of a close growth of diatoms. The most abundant diatom in this group was one of the stalked
Gomphonema. The basis of the covering is the gelatinous mass at the base of the stalked diatoms.
Scattered upon and through this mass were individuals of Nitzschia, and several olher diatomaceous
genera. An examination of the alimentary canal of Blepharocera tenuipes larvee always reveals scores or
hundreds of the siliceous tests of the diatoms. In the Colorado and California larvae of the various
Bibliocephala species and of Blepharocera jordant, the dorsal covering of diatoms is rather uncommon
though not infrequently to be seen.
The larve cannot live in stagnant or even quiet or slow running water. Indeed if, in the falling
of the stream, larve get stranded in a suddenly made pool or still, quiet-water part of the stream, they
soon die. They must have the highly erated, swift water of the stream’s center. They like the lip of a
fall, the rocks of cascades, and the sides of a pot-hole in which the water is ever whirling and boiling.
They can live therefore only in clear, swiftly running streams witha rapid fall, and this practically limits
these insects to mountain regions.
The pupæ (pl. 1, f. ro and 11) are found in the same places as the larvæ; that is, the larvæ, when
ready to pupate, do little more than arrange themselves, almost always in small or large groups, with
heads pointing down-stream, and there make the last larval molt. Each pupa is fastened to the rocks
by six pads, three on each lateral margin of the ventral aspect of the abdomen; these pads are not like
the suckers of the larva whose hold can be voluntarily loosened, but they permanently attach the pupa
to one spot. The pupa is even more extraordinarily shaped than the larva. It is strongly convex above,
with a dark brown or black, heavily chitinized body-wall, and is perfectly flat on its ventral aspect,
which lies smoothly against the rock. The wings and legs lie folded on the ventral aspect, which is
covered only by a thin colorless pupal cuticula. From the prothorax projects dorsally a pair of respira-
tory organs, each composed of four thin, double-walled plates, the outer plates of each set being strongly
chitinized, and acting as protecting covers for the two delicate membranous inner ones (the whole
arrangement like a two-leaved book, with board covers).
Of absorbing interest to the observer is the course of emergence of the adult from its submerged,
4 DIPTERA
fixed pupal case. Professor Comstock seems to have been the first to watch the process carefully, and he
describes it as follows :
« Each midge on emerging forced its way out through a transverse rent between the thorax and
abdomen. It then worked its body out slowly, and in spite of the swift current held it vertical. The
water covering the patch of pupæ varied from one-fourth to one-half inch in depth. In the shallower
parts the adult had trouble in working its way to the surface, still clinging to the pupa-skin by its very
long hind legs. While still anchored by its legs, the midge rests on the surface of the water for one or
two seconds and unfolds its wings; then freeing its legs it takes flight. The adults emerging from the
deeper water were swept away by the current before they had a chance to take wing. The time
required for a midge to work its way out of the pupa-skin varied from three to five minutes. »
As is obvious, the whole process of emergence and escape into free air must bea quick one.
Usually with insects it takes some time for the proper expansion of the wings, which are, in the pupa,
neither wider nor longer than the pupal wing-cases, but attain their full size only after withdrawal trom
these cases. But in the Blepharocerid there is no time for that; the slender legs cannot hold long
against the beating of the swift water, and so the remarkable condition of a full development and
expansion of the wings in the pupa obtains in this family. The fully developed wings lie in the pupal
case folded both longitudinally and transversely, and only need to unfold to be ready to carry the fly
into the safe air. It is this folding which produces the secondary veining of the wings characteristic ot
the family, this veining being simply the persisting creases and lines of the folding.
The writer has often watched the emergence of adults, and has been struck by the great loss
(apparently) of life in the process. So many flies are swept away by the swift water before the wings
can be unfolded or before the legs can be loosened from the pupal sheath, that it seems no wonder that
the family is a disappearing one. It is a case of the dangers of an extreme specialization. If the fixed
pupz lie in water too deep (easily occasioned by a sudden rise in the stream at the time for emergence),
or on the other hand, become wholly bereft of the life-giving water by a falling of the stream, there is
no hope for the fly. The first contingency seems indeed to be somewhat provided for by the apparent
power of the insect of postponing for some time, if necessary, its emergence. Thus, in the event of a
heavy rain and consequent rise of the stream, the too deeply submerged pupa may lie unchanged
until the water has run off (a matter which happens speedily in swift streams) to a safe shallowness.
The fully developed flies have been found numerously in the case of but few species. The flies
of Blepharocera tenuipes are found abundantly along certain small streams near Ithaca, N. Y., U. S. A.
The flies at rest cling by their long legs to the under sides of leaves on the bank from the water's edge
to eight or ten feet away. Of the hundreds of flies which were seen here in two or three visits all were
females; and they were engaged busily in feeding. This was accomplished by capturing on the wing
small Chironomid midges, and then returning to a leaf, where the unfortunate prey was lacerated by
the long, strong, saw-like mandibles, and the blood and body-juices drunk. The empty torn skin of the
prey was then dropped. As the males do not have mandibles, they must have a wholly different food
habit (probably non-predatory) and this may account for the absence of males from this feeding-ground.
The flight is rather slow and weak, a sort of timid fluttering. The flies of Bibiocephala elegantulus were
found by Kellogg to be numerous along the Big Thompson river, in the Rocky Mountains of Colorado,
U. S. A. The flies spent most of their time at rest on the vertical sides of the boulders from a few
inches to two feet above the water surface, but always where the rock face was frequently wetted by
the spray of the dashing water. The flies rested with legs and wings outstretched and body close to the
rock. The wings touched the rock face and, indeed, the attitude seemed to be adapted to bring as much
ofthe body as possible into contact with the wet, smooth face of the rock, as if to resist, by increased
friction, the tendency of the fly to slide down the vertical surface. None of these flies was seen feeding,
FAM. BLEPHAROCERIDZE 5
mating or egg-laying, although many hours were spent in watching them. They were most numerous
on bright, sunshiny days; on cloudy days the favorite rocks were often entirely deserted. The flight
is poor and numerous flies were caught readly in the hands.
Schnuse found the flies of both sexes of Afistomia elegans on composite flowers, sucking! But the
females were probably hunting small insects, not nectar or pollen. Scherfling and Bezzi have described
some of the habits of Hafalotherix lugubris found on the southern slopes of the Alps in North Italy. Males
were seen flying in and out of the foam of a falls at the tongue of a glacier; no females were with them.
As soon as the shadow of the mountains reached the falls the flies dissappeared. When at rest the flies
sit on stones and cliff walls near the stream with half opened wings and raised hind body. Females
appeared to bein much smaller numbers than males. Various mating pairs resting on the water were
washed by the waves on to the banks and often drowned. Several species of Hilara were found
associated in flight with Hapalothrix individuals and served as prey for them. Hapalothrix was found
flying from the end of May to the end of August, depending somewhat on the altitude.
For a satisfactory discussion of the feeding habits of these flies a knowledge of the anatomy of
the mouth parts is indispensable. The females of Blepharocera,like the females of Simulium,Ceratopogon
Dixa, Culex, and some other Nematocera, are bloodsucking, and while the mouth parts of these forms are
not strictly of biting type the mandibles are present as cutting or sawing or piercing organs. The males
of these forms are nectar-feeding, and have lost the mandibles. In the mouth parts (pl. 1, f. 13) of the
female Blepharocera all of the parts of the typical biting mouth are present, namely, the mandibles,
maxilla and labium. The mandibles are long and serrate on their inner edges so as to be effective
lacerating instruments. The maxillæ are elongate and blade-like, and have 4-segmented palpi. The
labium is, though somewhat elongated, truly lip-like, and has its terminal lobes not coalesced and
without pseudo-trachee. The hypopharynx is not short and tongue-like, as in the orthopterous mouth,
but is long and slender and stylet-like. Altogether the difference between the mouth parts of Blepharocera
and the typical biting type is one of modification, and of modification not sufficient to obscure the
homologies, although a modification more profound than that shown by the most generalized Lepidoptera
or Hymenoptera. On the other hand, there is not much difficulty in tracing the development of the
dipterous mouth from the generalized condition of Blepharocera (or Simulium, or Dixa, e¢a/.) to that extra-
ordinary specialized condition shown by Musca, where the mandibles and maxilla are lost, and the
labium is so modified that it has no longer any likeness to the lower lip of the orthopterous mouth.
With regard to the curious condition of the eyes of the adult Blepharocerids, the following is
taken from the account in the Extomological News (Kellogg. 1900) of the eyes of Blepharocera capitata :
« A specially interesting point in the imaginal anatomy of Blepharocera is the structural condition
of the compound eyes. It has long been observed that several flies (Simulium, Tabanus, e£ al.) and certain
other insects (Libellulidæ, Ascalaphus, Ephemeride, ef al.) have two sizesof facets in each compound
eye; and that some have the field containing these differently sized facets well delimited, the fields being
in some cases actually separated from each other by a non-facetted line or by a constriction. When this
constriction is so complete that the eye is truly divided, it may fairly be said that there are two pairs of
compound eyes, the two eyes of each lateral pair differing in the size of the facets. This last extreme
condition exists in the case of the males of certain Ephemeridæ and in both males and females of Ble-
pharocera capitata. (And in almost all other Blepharocerid species.)
» The eyes of Blepharocera are plainly divided; or it may be said that there are two on each
side (pl. 1, f. 12). One of these eyes is dark-colored, has small facets, and faces ventrally, anteriorly and
laterally. It is fairly convex. The other is reddish brown, is composed of much larger facets, faces
dorsally, and has a nearly flat surface. This red, large-facetted dorsal eye has the appearance of a
flattened mushroom head, or thick plate, resting above the other eye. In the males, the dorsal, large-
6 DIPTERA
facetted eye is much smaller and less conspicuous than in the female, but both parts of the eye (or both
eyes) are plainly present. This difference in the two parts of the eye is more radical, however, than can
be discovered by a mere examination from without. The ommatidia, or eye elements, of each of the
regions differ, as shown by sections, in several particulars. Corresponding with the difference in size of
the facets (the corneal lenses of the ommatidia), there is a marked difference in the diameter of the
ommatidia from the two regions. The ommatidia of the dorsal, large-facetted eye are nearly twice as
wide, and they are fully twice as long, as the ommatidia of the small facetted eye. Another striking and
important difference is that the larger ommatidia are very much less strongly pigmented than the
smaller ommatidia. There are, also, some differences in the character of the inner optic « layers » lying
between the hypodermal portion of the eye and the brain ; characters too technical for discussion here.
In sum, however, it is evident that there is so marked a difference in structure between the two eye
regions that there must be a difference in exercise of the function. The seeing by one of the eye regions
differs from the seeing by the other eye region.
» In brief discussion elsewhere of the «divided eyes of Arthropods» (Kellogg, Zool. Anzeig. 1898)
reference has been made to the observations of Chun (Bibliotheca Zool., 1896). who has described
the structure of the divided eyes of certain pelagic crustaceans, and to the observations of Zimmer
(Zeitschr. f.wiss. Zool., Bd.63, p. 236-262, 1898), who has studied the divided eyes of certain male May-flies.
In both of these cases the eyes show two sizes of facets, and accompanying this are both those other
structural difference which are apparent in Blepharocera viz., the large ommatidia and small amount of
pigment of the large-facetted eyes as compared with the small ommatidia and heavy pigmenting of the
small-faceted eyes. Here are three groups of Arthropods, viz., certain crustaceans, certain May-flies,
and the Blepharoceridæ, widely separated genetically and of widely varying habits, showing a common
structural modification of the eyes. We have evidently to do with independent adaptations determined
by some common functional need.
» The large size of the ommatidia and the small amount of pigment are characters which adapt
the large-facetted eyes for seeing in poor light (in the dark) and for readily perceiving moving objects
(delicate perception of shadows). The normal, small-facetted eyes see more accurately the actual shape
of visib'e objects; they have better definition, but require much light. Chun explains that the large-
facetted eyes of the pelagic crustacea enable them to perceive their prey (for the crustacea possessing
these eyes are all predaceous) in the poorly lighted levels of the water. The large facetted eves of the
male May-flies enable them, according to Zimmer's explanation, to perceive the advancing female during
the twilight marriage flight peculiar to these forms. What is the special use of the large-facetted eyes in
the case of Blepharocera ?
» The females are predaceous ; they capture other smaller live insects, and, lacerating them with
the saw-edge mandibles and blade-like maxillae, lap their blocd. The males, on the other hand, presu-
mably, do not capture insects; they have no mandibles, and are probably nectar-feeding. The female
might advantageously be possessed of a number of those large, weakly pigmented eye elements which
are specially adapted to the quick perception of moving objects. But what makes this explanation less
convincing is the fact that the males also possess these large-facetted ommatidia, although, to be sure,
in fewer number. Perhaps both males and females are active in twilight. Search as carefully as one
might, never but very few of the adult Blepharocera could be found along the stream, ‘from which they
were certainly issuing by thousands. Until the habits of our fly are better known, then, it is hardly
profitable to speculate on the special use of its large-facetted eyes ».
Distribution. — All the six species of Blepharoceridæ so far found in Europe occur in Italy or
adjoining islands; but most of them occur also elsewhere in southern or central Europe. Of the eleven
FAM. BLEPHAROCERIDZE 7
North American species one is found in the eastern (Allegheny). mountains, two in the middle (Rocky)
mountains and six in the western (Sierra Nevada and Coast Range) mountains and two in the West
Indies or Mexico. Beside the North American and European species, two species are found in Brazil
and one in Ceylon,
The Blepharoceridz are too unfamiliar to allow us to make any generalizations yet regarding
their distribution. Although so few species are known, three continents are included in the range of the
family. These conditions suggest that we have to do with a family probably formerly including nume-
rous species scattered over the world, but now dying out, a species persisting here and there through the
wide range. These persisting species agree remarkably in the habits of the immature stages, and indicate
in just what kind of habitat we should look for other members of the family in regions from which as yet
no Blepharoceridæ are recorded. The great loss of larva and pupæ by the drying up or contamination
of streams and the enormous loss of the issuing flies carried away by the current at the time of emer-
gence from the pupa are evidently factors in the peculiar life of these insects tending to prevent them
from holding their own. The larvæ and pupæ live shallowly submerged only in swiftly running, clear,
fresh water; such conditions are provided by all, or nearly all, mountain or hill brooks and hardly
anywhere else. As the known species extend from the Equator to sub Arctic latitudes, temperature or
climate offer probably no barriers, nor probably does altitude, the North American species alone ranging
from nearly sea-level to 8000 feet above sea-level.
Desiderata. — There must be several living species of this family yet to be found. In a single
summer's attention to the streams in the low mountains near Stanford University, California, the writer
was able to add as many species to the North American fauna as had been known before from the
whole country. Wherever there are mountains or hills with swift, clear streams one can almost assert
that Blepharoceridæ will be found. In America the streams of the Ozarks, the Georgia hills, the Tennes-
see and North Carolina mountains, the Cascades and Olympics of Puget Sound regions, the Rockies of
New Mexico and Arizona and the mountains of Southern California should all be examined. Wherever
in the world explorers or collectors are penetrating into mountain regions these insects should be looked
for along the streams and cascades.
With additional species and a widened distribution of old forms known, classification can be
revised and more satisfactorily founded.
The life-history of no Blepharoceridz is fully known; the first eggs of any species are yet to be
found; the food habits of the males are unknown; a host of observations on the habits are to be made.
No one has studied the « secondary venation », the creasing of the wings. Are these lines of
folding uniform in the species, genus, family? Are there classificatory characters to be derived from
them? What is the significance of the little chitinous thickening or knot in the re-entrant angle of the
anal margin of the wing?
Do the well-developed and plainly differing external genitalia, especially those of males, offer
characters which can be used in classification? This is practically certain, but as yet no one has even
attempted their use.
Classification. — The nine genera are readily separable into two principal groups on the basis
of a venational character. The characters drawn from the veins and eyes are chiefly depended on to
distinguish the genera.
[9 0)
DIPTERA
TABLE OF GENERA
No incomplete vein near the posterior margin of the wings (= an incom-
plete media; lacking).
Eyes bi-sected by an unfacetted cross-band or line into a dorsal brownish
region of larger facets and a lower black region of smaller
facets.
A longitudinal vein between the first and fourth veins (= radial )
vein at least two-bvanched). . . . . . . . . . I. Genus ApıstomyIa, Bigot, p. 8.
No longitudinal vein between the first and fourth veins (— radial
vein unbranched) . . . 2 . . . . . . . . 2. Genus HAMMATORHINA, Loew, p. 9.
Eyes not bi-sected by an unfacetted cross-band; a longitudinal vein
between the first and fourth veins (— radial vein branched).
Eyes separated by a broad front.
Proboscis long, palpi but little developed . . . . . . . . 3. Genus ParrosTOMA, Schiner, p. 9.
Proboscis not longer than the vertical diameter of the head ; well
developed four-segmented palpi. . . . . . . . . 4. Genus Kerrocerna, Williston, p. 10.
Eyes contiguous.
Ungues of the ordinary structure ; tibie with spurs at the tip . . 5. Genus Curupira, F. Müller, p. ro.
Ungues abnormal, pulvilliform; no spurs at the tip of the tibie . 6. Genus HAPALOTHRIX, Loew, p. 10.
An incomplete vein near the posterior margin of the wings (= an incom-
plete medias present).
Second longitudinal vein with two branches (— radius, partly distinct);
a cross-vein connecting veins 4 and 5 (= a medio-cubital
cross-vein).
Anterior branch of second vein and veins 2 and 3 all separating at
a common point or close together (vadius,, vadius, and
radius, all separating at a common point or close together). 8. Genus BIBIOCEPHALA,O.-Sacken,p.13.
Second longitudinal vein simple, without branches (= radius, wholly
fused with radiuss). —
No cross-vein connecting veins 4 and 5 (— no medio-cubital cross-
vem) . 2 x4 s ee we 3 09 D GEDUS BLEPHAROCERA, Miacquantspacis
A cross-vein connecting veins 4 and 5 (= a medio-cubital cross-
VEN) Ino cx. LENS TN OR NT 9.2GEenUsTEHIEORUSTRellocerap EON
I. GENUS APISTOMYIA, BIGOT
Apistomyia. Bigot, Ann. Soc. Ent. Fr. (4), Vol. 2, p. 100, pl. 1, f. 1 (1862); Loew, Boll. Soc. Ent.
Ital, Vol. 1, p. 97, pl. 2, £. 1-3: (1869); Loew, Schles. Zeitschr..t. Font NF VOLU Ep MOT
pl. 1, f. 1 (1877), Osten-Sacken, Berl. Ent. Zeit. Vol. 36, p. 410 (1891) and Vol. 40, p. 162 (1895);
Sknuse, Zeitschr. f. Hym. u. Dipt. Vol. 1, p. 145 (1901), ISertész Cat Dipts\.0]. 1,9225
(1902) (elegans).
Characters. — No incomplete vein near the posterior margin of the wings; eyes bisected by
an unfacetted cross band or line into a dorsal brownish region of larger facets and a lower black region
of smaller facets; a longitudinal vein between the first and fourth veins.
FAM. BLEPHAROCERIDZE 9
Biology. — Both males and females have been found. Life-history and immature stages
unknown. Schnuse found both sexes at composite flowers, sucking. But the females were probably
not there for nectar, but hunting small iusects, as they are blood-drinkers.
Geographical distribution of species. — The single species of the genus is recorded, so
far, only from the islands of Corsica and Cyprus.
1. A. elegans, Bigot, Ann. Soc. Ent. Fr. (4), Vol. 2, p. 110, pl. 2, f. 1 (1862) (Corsica, Cyprus). —
Pll Ris; 16; Pl. 2, hig. 20;
2. GENUS HAMMATORHINA, LOEW
Hammatorhina. Loew, Boll. Soc. Ent. Ital. Vol. 1, p. 94, pl. 3, f. 3-6 (1869); Loew, Schles. Zeitschr.
fh Bote NISE2VOol 6, p. 75. ple te 2 (1877); Osten Sacken, Berl. Ent. Zeitschr. Vol. 36, p. 189
and p. 411 (1892); Osten-Sacken, Berl. Ent. Zeitschr. Vol. 40, p. 162 (1895); Kertész, Cat.
Dipt. Vol. 1, p. 284 (1902) (bella).
Tanyrhina. Loew, Mon. N. Amer. Dipt. Vol. 1, p. 8 (1862).
Characters. — No incomplete vein near the posterior margin of the wings; eyes bisected by
an unfacetted cross band or line into a dorsal brownish region of larger facets and a lower black region
of smaller facets; no longitudinal vein between the first and fourth veins.
Biology. — Only the male sex of this genus is known. Life-history unknown. At the Oct. r,
1890 meeting of the London Ent. Society « Mr. C. J. Gahan exibited a curious little larva-like creature
found by Mr. A. P. Green in a rapid mountain stream in Ceylon, and observed that there was some
doubt as to its true position in the animal kingdom. » Thereupon the savants of the Society proceeded
to make guesses as to the general identity of this little Ceylonese visitor. Mr. Hampson pointed out its
likeness to chaetopod worms (especially because of the parapodia-like lateral appendages) but added that
all the known polychaetous worms were marine. Lord Walsingham and Mr. McLachlan expressed the
opinion that the animal was of myriapodous affinities, and was not the larva of an insect. After this
meeting Mr. Gahan had his specimen examined by Baron Osten-Sacken and Professor Packard, who
recognized it as a Blepharocerid larva. As Hammatorhina bella is the only Blepharocerid species so far
found in Ceylon Mr. Gahan's specimen may provisionally be looked on as the larva of this species.
Geographical distribution of species. — The single species of this genus is recorded, so
far, only from Ceylon.
I. H. bella, Loew, Boll. Soc. Ent. Ital. Vol. 1, p. 96 (1869) (Ceylon). — PI. 2, Fig. 17, 27.
3. GENUS PALTOSTOMA, SCHINER
Paltostoma. Schiner, Verh. Zool.-Bot. Ges. Wien, Vol. 16, p. 931 (1866); Loew, Boll. Soc. Ent. Ital.
Moll p 05 pl. 2, f. 7 and 8 (1869); Loew, Schles. Zeitschr. f. Ent. Neue Folge, Vol. 6,
posu sod pl. 1,0. 7 (1877)\> Osten-Sacken, Berl. Ent. Zeit., Vol. 36, p. 419 (1892); Osten-
Sacken, Berl. Ent. Zeit. Vol. 40, p. 162 (1895); Kertész, Cat. Dipt. Vol. 1, p. 284 (1902);
Aldrich, Cat. N. Amer. Dipt. p. 171 (1905) (superbiens).
Characters. — No incomplete vein near the posterior margin of the wings; eyes not bisected
by an unfacetted cross band; a longitudinal vein between first and fourth veins; eyes separated by a
broad front; proboscis long, palpi but little developed.
10 DIPTERA
Biology. — Only males of this genus known. Life-history and immature stages unknown.
Geographical distribution of species. — Of the two known species one is recorded only
from St. Vincent Id., West Indies, the other from Columbia, S. A., and, doubtfully, from Mexico.
I. P. schineri, Williston, Trans. Ent. Soc. Lond. p. 296, pl. 8, t. 27, 27a, 27b (1896). (St. Vincent Id.,
West Indies). — Pl. 2, Fig. 26.
2. P. superbiens, Schiner, Novara Reise, Dipt. p. 28, pl. 2, f. 4 (1869) (Columbia, South America, and
Mexico [?]). — Pl. 2, Fig: 21;
4. GENUS KELLOGGINA, WILLISTON
Kelloggina. Williston, Journ. New York Ent. Soc. Vol. 15, (1907) (rufescens).
Snowia. Williston, Kansas Univ, Quart. Vol. 1, p. 119 (1893); Osten-Sacken, Berl. Ent. Zeit. Vol. 40,
p. 162 (1895) (rufescens).
Sackienella. Williston, Trans. Ent. Soc. Lond. p. 270 (1896); Kertész, Cat. Dipt. Vol. 1, p. 284 (1902)
(rufescens).
Characters. — No incomplete vein near the posterior margin of the wings; eyes not bisected
by an unfacetted cross-band; a longitudinal vein between first and fourth veins; eyes separated by a broad
front; proboscis not longer than the vertical diameter of the head, well developed 4-segmented palpi.
Biology. — Female only known. Life-history and immature stages unknown.
Geographical distribution of species. — The single known species in this genus (represented
by a single female specimen) is recorded from Rio de Janeiro, Brazil.
I. K. rufescens, Williston, Kansas Univ. Quart. Vol. 1, p. 290 (Snowia) (1893) (Rio de Janeiro).
5. GENUS CURUPIRA (F. MULLER), OSTEN-SACKEN
Curupira (F. Müller). Osten-Sacken, Berl. Ent. Zeit. Vol. 40, p. 162 (1895); & p. 165 ff. of same
reference; Kertész, Cat. Dipt. Vol. 1, p. 284 (1902) (forrentium).
Paltostoma. Brauer, Zool. Anz. Vol. 3, p. 134 (1880); F. Müller, Kosmos, Vol. 8, p. 37, figs. (1881);
F. Müller, Arch. Mus. Nac. Rio Janeiro, Vol. 4, p. 47, pl. 4-7 (1882) (torrentium).
Characters. — No incomplete vein near the posterior margin of the wings; eyes not bisected
by an unfacetted cross-band; a longitudinal vein between the first and fourth veins; eyes contiguous;
ungues of the ordinary structure; tibiæ with spurs at the tip.
Biology. — Males and females, and larvæ and pupæ known. The anatomy of larvæ and pupæ
exhaustively studied by F. Müller (Arch. Mus. Nac. Rio Janeiro, Vol. 4, p. 47 ff., pl. 4-7, 1882).
Larva and pupa found abundantly in the Garcia, Jordao and Caeté rivers in the province of Santa
Catherina, Brazil.
Geographical distribution of species. — The single species of this genus so far known is
recorded only from Brazil.
I. C. torrentium, F. Müller; Brauer, Zool. Anz. Vol. 3, p. 134 (1880) Brazil). — Pl. 2, Fig. 24.
6. GENUS HAPALOTRHIX, LOEW
Hapalothrix. Loew, Deutsche Ent. Zeitschr. Vol 20, p. 211 (1876); Loew, Schles. Zeitschr. f. Ent.
N. F. Vol. 6, p. 81, pl. 1, f. 8 (1877); Osten-Sacken, Berl. Ent. Zeitschr. Vol. 36, p. 411 (1892);
FAM. BLEPHAROCERIDE II
Osten-Sacken, Berl. Ent. Zeit. Vol. 40, p. 162 (1895); Bezzi, Zeitschr. f. Hym. u. Dipt. Vol. 1,
p. 275 (19o1); Kertész, Cat. Dipt. Vol. 1. p. 285 (1902) (lugubria).
Characters. — No incomplete vein near the posterior margin of the wings. Eyes not bisected
by an unfacetted cross band; a longitudinal vein between first and fourth veins; eyes contiguous;
ungues about normal, pulvilliform ; no spurs at the tip of tibia.
Biology. — Males and females known. Life-history and immature stages unknown. Loew writes,
« Herr Scherfling entdeckte diese interressante Art am rr. Juli an der Südseite des Monte Rosa in der
Nähe von Macuguaga in einer Meereshóhe von etwa 6000 Fuss. Die Mànnchen derselben trieben sich
da, wo der Gletscherbach aus dem unteren Gletscher hervorkommt, auf dem vom schnell abwärts
strómenden Wasser erzeugten Schaune in ziemlicher Anzahl spielend herum; sie waren wegen der
schweren Zuganglichkeit der Stelle gar nicht leicht zu erlangen; zuweilen von spritzendem Wasser
getroffen und mit fortgenommen, kehrten sie doch stets bald auf die alte Stelle und zu dem altem
Spiele zurück. Weibchen waren, trotz aller längere Zeit hindurch darauf verwendeten Sorgfalt nicht zu
entdecken. Das Spiel der Männchen währte so lange, die Stelle von der Sonne beschienen wurde,
ununterbrochen fort; sobald diese aber soweit gesunken war, dass der Schatten der Berge den
Tummelplatz traf, hórte das Spiel so fort auf, und sämtliche Männchen waren gar bald wie vóllig ver-
schwunden. » Bezzi writes, « Ich habe Hapalothgix lugubris am 13. Juli d. J. bei Chiesa in Valmalenco
(Sondrio), auf einer Meereshóhe von etwa 1000 Meter, unter ähnlichen Umständen wie H. Scherfling
gefunden; nur kein Gletscher war hier in der Nähe; und die Lebensdauer der Thiere schien länger zu
sein, da ich die Art an derselben Stelle noch am 21. Juli zahlreich beobachten konnte. Die Mànnchen
halten beim Flug die hinteren Beine so gestellt, wie einige Arten der Gattung Bibio. In der Ruhe sitzen
sie an Steinen und Felsstücken ganz nahe dem Strome mit halbgeöffneten Flügeln und erhobenen
Hinterleibe. Die Weibchen sind in viel geringerer Zahl vorhanden, als die Männchen. Die begattung
findet auf dem Wasser statt; und die copulirten Párchen werden von den Wellen hier und da ans Ufer
gebracht und oft auch verschlungen. Die fünf Weibchen, welche ich gefangen habe, waren alle in
Copula und wurden von den Wellen getragen. Wo die Weibchen sitzen oder fliegen habe ich mit
Sicherheit nicht in Erfahrung bringen kónnen. In Gesellschaft mit Hapalothrix fliegen einige Hilara
Arten; und die ersteren werden oft von letzteren erbeutet... Das Verbreitungsgebiet von Hapalothrix
wird hewiss auf der ganzen Südseite der Alpen zu suchen sein. sie lebt wahrscheinlich an allen grósseren
Gewässern, welche von den Gletschen herabfliessen. Ihre Verwandlung wird gewiss im Wasser statt-
finden und durfte nicht sehr verschieden sein von derjenigen der brasilianischen Arten, welche
Dr. Fritz Müller beschreibt. Die Flugzeit wird je nach der Hóhe von Ende Mai bis Ende August
reichen; die Art wird gewiss auch nicht ohne praktischen Nutzen sein, indem sie der alpinen Forelle
als Nahrung dienen durfte. »
Geographical distribution of species. — The single known species of this genus has been
taken near Macuguaga (Italy) (alt. 2000 m.) on the south side of Monte Rosa, and at an altitude of
1000 m. near Sondrio (Italy).
I. H. lugubris, Loew, Deutsche Ent. Zeitschr. Vol. 20, p. 212 (1876) (Northern Italy). — PI. 2, Fig. 18;
Plis2, Fig. 28.
7. GENUS BLEPHAROCERA, MACQUART
Blepharocera. Macquart, Ann. Soc. Ent. Fr. (2) Vol. 1, p. 61 (1844); (amended in 1862 by Loew
to Blepharocera) (fasciata).
Asthenia. Westwood, in Guérin Mag. Zool. (2) Vol. 4, pl. 94 (1842) (fasciata).
12 DIPTERA
Asyndulum. Walker, List Dipt. Brit. Mus. Vol. 1, p. 86 (1848) ( fasciata)
Liponeura (in part). Loew, Stett. Ent. Zeit. Vol. 5, p. 118 (1844) (cinerascens).
Blepharocera (Macquart). Loew, Boll. Soc. Ent. Ital. Vol. r, p. 85 (1869); Loew, Schles. Zeitschr.
f. Ent. N. F. Vol. 6, p. 54, pl. 1(1877)5. Osten-Sacken, Berl. Ent: Zeit. Vol. 40, pP. 149 (1855);
Kellogg, Ent. News. Vol. 10, pp. 305-318, f. 5 (1900); Kertész, Cat. Dipt. Vol. 1, p. 282 (1902);
Kellogg, Proc. Calif. Acad. Sc. (3), Zool. Vol. 3, pp. 187-223, pl. 18-22 (revision of the genus)
(1903); Aldrich, Cat. N. Amer. Dipt. p. 171 (1905) ( fasciata).
Characters. — Incomplete vein near the posterior margin of the wings; second longitudinal
vein simple without branches ; no cross vein connecting veins four and five.
Biology. — Males and females, and larvæ and pupæ known. Anatomy of larvæ, pupæ and imago
studied by Dewitz (Berl. Ent. Zeitschr. Vol. 35, pp. 61-66, pl. 3-4, 1880), and Weirseijski (Krakow,
1881), for B. brevirostris Loew, and by Kellogg (Ent. News. Vol. ro, pp. 305-318, f. 5, 1900; and Proc.
Calif. Acad. Sc., (3), Zool. Vol. 3, pp. 187-233, pl. 18-22, 1903) for B. tenuipes. Dewitz found larvae
and pupz in the Ockerthal near Goslar (Harz Mts.) fastened to loose stones in the swift water, and
imagines flying about over the stream and often settling on projecting rocks. Riley found (1881) larvae
and pupe of B. tenuipes near Watertown, New-York (U.S. A.), and Constock has long known them at
Ithaca, New-York (U. S. A.) Kellogg has found the immature stages of B. fenuipes at Ithaca and in the
Riviere des Chiens near Quebec, and of B. jordani in many streams near Stanford University, in the
Coast Range (60 miles away), while Grinnell has found them in a mountain stream near Pasadena in
Southern California. Kellogg records the immature stages of B. Osten-Sackeni from several streams in
Northern, California. He noted young larvae of B. tenuipes 2.5 mm. long in Coy Glen stream near
Ithaca, New-York on May 9; on May 14 the first pupæ were noted; on May 20 the pupa outnumbered
the larvæ, and on fune 1 the'first flies issued, most of the pupe being transformed by June 9. On June
27 many female flies were found feeding along another near-by stream. Both of these streams were
carefully watched through the rest of the summer and all the autumn, but no other generation appeared.
Do the frail imagines live through the winter? The larvæ of B. jordani Kell, have been found by Kellogg
in Los Gatos Creek near Stanford University, California, as early as Feb. 23 and as late as June r
(Stevens Creek, an adjoining stream), and at various times in the intervening three months. Pupæ were
first found in these streams on April 1 and as late as June 4.
The females of B. tenuipes catch small Chironomid mites on the wing, lacerate their bodies and
drink the body juices. The feeding of the males has not been observed.
Geographical distribution of species, — Of the six species assigned to this genus three are
European and three North American.
I. B. fasciata, Westwood, Mag. Zool. (2), vol. 4, pl. 94 (Aesthenia) (1842) (Europe). Type species. —
Plo; Fig..43 P2 EIBpE2 B:
limbipennis, Macquart, Ann. Soc. Ent. Fr. (2), vol. 1, p. 63. pl. 3 (1843).
. B. cinerascens, Loew, Stett. Ent. Zeit. Vol. 5, p. 118, pl. 1, f. 6-10 (Liponeura) (1844) (Europe).
fasciata, Schiner, Fauna Austr. Dipt. Vol. 2, p. 638 (excl. male) (1864) (Blepharicera).
limbinervis, Macquart, Ann. Soc. Ent. Fr. (2), Vol. 2 p. 69, pl. 3 (1844) (Blepharicera).
3. B. brevirostris, Loew, Schles. Zeitschr. f. Ent. N. F. Vol. 6, p. 67 (Liponeura) (1877) (Central Europe :
Bohemia, Silesia).
4. B. tenuipes, Walker, List Dipt. Brit. Mus. Vol. 1, p. 86 (Asyndulum) (1848) (Northeastern United
States and Eastern Canada). — PI. I, Fig. 7, 12.
capitata, Loew, Berl. Ent. Zeitschr. Vol. 7, p. 298 (1863).
3. jordani, Kellogg. Proc. Calif. Acad. Sc. (58), Zool. Vol:3, p. 189; pl. 18; f pro ES, pl. 20;
fig. 1 and 2 (1903) (California). — Pl. I, Fig. 8,9. —
6. B. osten-sackeni, Kellogg, Proc. Calif. Acad. Sc. (3), Zool. Vol. 3, p. 191, pl. 18, f. 2, pl. 19, f. 2,
pl. 20, f. 3 and 4 (1903) (California).
hj
Cn
M
FAM. BLEPHAROCERIDÆ 13
8. GENUS BIBIOCEPHALA, OSTEN-SACKEN
Bibiocephala. Osten-Sacken, Geol. Survey of the Terr. for 1873, p. 564 (1874); Loew, Schles. Zeitschr.
f. Ent. N. F. Vol. 6, p. 95 (1877); Osten-Sacken, Berl. Ent. Zeit. Vol. 36, p. 409 (1892)
Vol. 40, p. 161 (1895); Kertész, Cat. Dipt. Vol. 1, p. 281 (1902); Kellogg, Proc. Calif. Acad. Sc.
(3) Zool. Vol. 3, pp. 187-221, pl. 18-22 (1903) (revision of the genus); Aldrich, Cat. N. Amer.
Dipt., p. 171 (1905) (grandis).
Agathon. Röder, Wien. Ent. Zeit. Vol. 9, p. 230 (1890) (elegantula).
Characters. — An incomplete vein near the posterior margin of the wings; second longitudinal
vein with two branches; cross vein connecting veins four and five; anterior branch of second vein, and
veins two and three all separating at a common point or close together.
Biology. — Males and females and pupæ known. On June 22 to 25 (1901) Kellogg found
imagines of B. elegantula numerous among the boulders of Big Thompson stream, Estes Park, Colo-
rado (altitude 7,500 feet), where the stream breaks through the Willow Park terminal moraine. At this
time, old pupæ and empty pupal skins were found, but no larvae except two very young ones. On
August 10 to 12, the flies were found still common and numerous larvæ, young and old, but no pupa.
In three other nearby mountain torrents, viz. Wind Creek, Mill Creek and South Fork of Big Thompson,
adults and old pupa were found. A note made at this time is as follows : « It seems to me that I have
got here just as the last adults of one generation are issuing, and that the larvæ of August are larvæ
from eggs laid by these adults. This would mean a generation of flies appearing about July 1, say, and
a second one appearing later, say about September 15. » This is, of course, mere conjecture.
The larva of B. doanei were taken as early as February 25 (Los Trancos Creek, California), and
as late as July 26 (Red Cap Creek, Hoopa Indian Reservation, Humboldt County, California), and in
all the intervening months; pupa are first recorded March 31 (Campbell Creek, California) and from
then till July 26 (Red Cap Creek, Humboldt County, California); the only free-flying imago was taken
on July r5 (Congress Springs, Campbell Creek, California).
Kellogg's earliest recorded date of taking the laryæ of B. comstocki is February 11 (Alembique
Creek, California), the latest April 3o (Stevens Creek, California); the earliest pupæ are of the date
February 27 (Los Gatos Creek. California). A free-flying imago was taken April 6 (Saratoga Springs,
Campell Creek, California).
Geographical distribution of species. — The four species included in this genus are all
North American coming from the Rocky, Sierra Nevada and Coast Range mountains of Colorado, New
Mexico and California.
I. B. grandis, Osten-Sacken, Geol. Survey of the Terr. for 1873, p. 566, fig. (1874) (Colorado, New
Mexico, Utah, Idaho).
. B. comstocki, Kellogg, Calif. Acad. Sc. (3), Vol. 3, p. 192, pl. 18, f. 6 and 7, pl. 20, f. 5 and 6, pl. 21,
ia ngo3)r(Galitormia)4 — Pl. I, Figs, 2, 5, 6,11.
3. B. doane, Kellogg, Psyche, Vol. 9, p. 39 (1900) (Liponeura) (California). — Pl. I, Fig. 10, 13;
prae: 29:
4. B. elegantula, Róder, Wien. Ent. Zeit. Vol. 9, p. 230 (1890) (Agathon) (Sierra Nevada Mountains,
Idaho, Colorado). — Pl. 2, Fig. 14, 15, 19.
l3
14 DIPTERA
9. GENUS PHILORUS, KELLOGG
Philorus(1). Kellogg, Proc. Acad. Sc. Calif. (3), Zool. Vol. 3, p. 199 (1903) (bilobata).
Liponeura (in part). Loew, Stett. Ent. Zeit. Vol. 5, p. 118 (1844) (bilobata). |
Blepharocera (in part). Macquart, Ann. Soc. Ent. Fr. (2), Vol. 1, p. 61 (1843) (ancilla).
Characters, — An incomplete vein near the posterior margin of the wings; second longitudinal
vein simple, without branches; a cross-vein connecting veins 4 and 5.
Biology. — Males and females and larvæ and pupæ known. Osten Sacken’s specimens of
P. yosemite were three males caught on the wing on the bridle-path to the foot of the upper Yosemite
Fall (California), 3 p. m., June 6, 1876. No other specimens of this species are recorded until 1903 when
Kellogg records (Psyche, Vol. 10, p. 186) the finding on July 15 of larve and pupe (and male and
female flies dissected out from pupæ just ready to transform) in the King’s River Canon (another great
California canon of the western slope of the Sierra Nevada about 60 miles south of the Yosemite). These
larvæ and pupæ were taken from the smooth submerged surfaces of great granite blocks fallen into a
swift, little, clear-water stream called Granite Creek which flows into King’s River.
Geographical distribution of species. — Of the three species included in this genus one is
found in Europe and two in the mountain region of the western United States.
1. P. bilobata, Loew, Boll. Soc. Ent. Ital. Vol. 1, p. 97 (1869) (Liponeura) (Southern Europe : Greece,
Italy). — Pl. 2, Fig. 22.
2. P. ancilla, Osten-Sacken, Cat. N. Amer. Dipt. (2 ed.), p. 266 (1878) (Blepharocera) (California).
3. P. yosemite, Osten-Sacken, Bull. U.S. Geol. Survey, Vol. 3, p. 195 (1877) (Liponeura) (California,
U. S. A‘, Yosemite Valley):
(x) Professor Aldrich writes me that the name PArloros was used by Walker in 1854 for a Lepidopterous genus, but the difference in spelling,
slight as it is, constrains me to hold to the present generic name.
INDEX
Pages. Pages Pages.
Agathon (genus), Röder 13 elegans, Bigot (g. Apistomyia) 9 osten-sackeni, Kell. (g. Blepharo-
Apistomyia (genus), Bigot 8 elegantula, Röder (g. Bibiocephala) 13 cera) T2, 10
Asthenia (genus), Westw. II
Asyndulum (genus), Walk. 12 fasciata, Westw. (g. Blepharocera) I2 Paltostoma (genus), Brauer B
ancilla, O.-S. (g. PAilorus 14 fasciata, Schiner (g. Blepharocera) 12 Philorus (genus), Kell.
Blepharocera (genus), Macq. 11, 14 grandis, O.-S. (g. Bibiocephala) D3 rufescens, Will. (g. Kelloggina) Io
EW torhi
bella, Loew (g. Hammatorhina) 9 Mamma tonninall ccna Slicer x |
brevirostris, Loew (g. Blepharocera) 12 . Sackienella (genus), Will. 10
i Hapalothrix (zenus), Loew 10 RES
Bibiocephala (genus), O.-S. 13 schineri, Will. (g. Paltostoma) IO
i r (g lorus : i Vill. IO
bilobata, Loew (g. Philorus) I4 jordani, Kell. (g. Blepharocera) 2 Snowia (genus), Will
superbiens, Schiner (g. Paltostoma) 10
Curupira (genus), O.-S. 10 Kelloggina (genus), Will 10
cinerascens, Loew (g. Blepharocera) 12 Tanyrhina (genus), Loew 9
capitata, Loew (g. Blepharocera) 12 limbicornis, Macq. (g. Blepharocera) 12 torrentium, Brauer (g. Curupira) 10
comstocki, Kell. (g. Bibiocephala) 13 limbipennis, Macq. (g. Blepharocera) 12 tenuipes, Walk. (g. Blepharocera) 12
Liponeura (genus), Loew r2
doanei, Kell. (g. Bibiocephala) 165) lugubris, Loew (g. Hapalothrix) II yosemite, O.-S. (g. Philorus) 14
Ls
© 00-1 Oc CU BR WN
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FAM. BLEPHAROCERIDE 15
EXPLANATION OF PLATES
IERANET:
Head of Bibiocephala comstocki, Kellogg, Q (after Kellogg).
= a= — — Cf (after Kellogg).
— Apistomyia elegans, Bigot, Q (after Schnuse).
= Blepharocera fasciata, Westwood, © (after Loew).
. Larva of Bibiocephala comstocki, Kellogg, dorsal aspect; ant., antenna; /. p., lateral processes.
— — -— — ventralaspect;. g., tracheal gills; s., sucker (after Kellogg).
. Blepharocera tenuipes, Walker, cy (after Kellogg).
. Larva of Blepharocera jordani, Kellogg, dorsal aspect (after Kellogg).
= = — — ventral aspect (after Kellogg).
. Pupa of Bibiocephala doanet, — dorsal aspect (after Kellogg).
— — comstocki, | — — — (after Kellogg).
. Section through compound eyes and brain of head of Blepharocera tenuipes, Walker, showing
difference in character of ommatidia in the two parts (dorsal and ventral) of each eye;
o., ocelli; br., brain; /. f., large facets; s. f., small facets; o. /., optic lobes (after Kellogg).
Mouth parts of Bibliocephala doanet, Kellogg, Q ; md., mandible; mx., maxilla; mx./., maxillary
lobe; mx.p., maxillary palpus; /7., labium ; fg., paraglossa; kyp., hypopharynx; /. ep., labrum-
epipharynx (after Kellogg).
PLATE 2;
. External genitalia of female Bibiocephala elegantula, Röder, dorsal aspect (after Kellogg).
m. ME male = = = — (after Kellogg).
. Antenna of male Apystomia elegans, Bigot (after Bigot).
— — Hammatorhina bella, Loew (after Loew).
. Tip of fore-leg of male Hapalothrix lugubris, Loew (after Loew).
. Bibiocephala elegantula, Röder, © (after Kellogg).
. Venation of Apistomyia elegans, Bigot (after Schnuse).
-—- Paltostoma superbiens, Schiner (after Schiner).
— Philorus bilobata, Loew (after Loew).
— Bibiocephala doanei, Kellogg (after Kellogg).
— Curupira torrentium, Müller (after Müller).
— Blepharocera fasciata, Westwood (after Loew).
= Paltostoma schineri, Williston (after Williston).
— Hammatorhira bella, Loew (after Loew).
— Hapalothrix lugubris, Loew (after Loew).
Stanford University, Calif., U. S. A., March 15, 1907.
GENERA INSECTORUM
2
DIPTERA
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