Fe he old an Wet opeded ee teahedty aig i aster we itt) Ae ry gta Uy REY Fee $Y £ if ithe aaa ne ties Apirpeay tee fae eee at ey it ee PHL R Rear Minette ite vein h ty! di aie ie ae a ; ABs a pe ae Baas an ret ay rte Re a ar EA Oty Psa eOtia in gag Hae . aa had { { Mi ! ne ty } aby, i F ‘ - i . i« ‘ae : sf bey ‘ 4) lye 4 ral " Medel i ‘ 4b) : ' : f ‘ 4 85 t 4 ae 8 1 uit ‘ st fr * MST Au melptiely He Shit steht Certs i aetnse Pettencas ; byt By f ab) 42 Aas ratanye sae Ta ve} fae! * : trp tak mite tna Winviee Me { ¢ i ened ; J 4" 4 Bey cd Aelerat CORTE a ! 2 adi: | ; ‘ ; ; ; Hath r th i Me! We Caan j en AOL sib a Hants int : att Tadd } i a eae eee ee 7) te vi i F pre Sy toe x j Mae P3 ksh se eal ed aia he peewee [igh Ae Ra aie! paul mat ogi pee pb tig AM tS Let ; on 1) Pod =e % , * é om, * ? ke > i 7, oo Presented to Library of the ity of Coronte The Univers by E.M. Walker Digitized by the Internet Archive in 2009 with funding from University of Toronto http://www.archive.org/details/canadianentomolod54ento ~ \ a) Olle ae Pal ae Che Canadian Entomologist VOLUME LIV 5 72 1922 EDITED BY J. McDUNNOUGH, Entomological Branch DEPARTMENT OF AGRICULTURE OTTAWA, ONTARIO. _ EprrortaAL COMMITTEE: A. W. Baker W. H. Brittain L. Caesar N. Criddle A. Gibson F. J. A. Morris F. C. Trelherne A. F. Winn Editor Emeritus: REV. C.J. S. BETHUNE. ORILLIA, ONTARIO. CURRAN BROS. 1923 QL 46! C2H Vlaams 628980 23.756 List of Contributors to Volume LIV. BES PIS eee WV) oho iiicar a ccreusceaursoncdacscss=see U. §S. Entomological Laboratory ............ San Antonio, Texas. JEAN TSS bs eeesvo te te eres Museum of Comparative Zoology ............ Cambridge Mass. EST TOOT EIN hp ET. | cc uccacercesancyessesvee Apricnitural COUGEHi...c--c-csescsnuewersecanenetarsouse Mississippi. RSE Gs IETD Wo NCES | =~ osccss qeceanoens~uce Gmiversity Of. Toronto) o:..cneseeebactussaedecaertay er ces cakmeseaaceaseneeaceaemreee Indianapolis, Ind. PEER PENS er EO Senco Goce nuusoescecuac choke wcanite enciisepecenustucacnieusbeegtesercesessheueseeszeaemecmmeceereet Cincinnati, Ohio. are P RN iy Ny rennet encectnceeseessce-ulwntereavctwucactcaaeccesceace Fon boestatiee sean ungee ceo nap reeeenaees Longmeadow, R. I. Seer P NG Hee NV IGP paccoade nu seas ecctcuaescave-csse Dominion Entomological Laboratory ........ Lethbridge, Alta. CRP WaRtGi Wie OB. -iccsccceccsice U. S. Entomological Laboratory ...............- West Lafayette, Ind. CHAMIBEREEN, RR. Ve -scccecccocscccssee Museum of Comparative Zoology ............ Cambridge, Mass. Ree See WE PERE AS ES, | ou odessaca-cusc0eres Bureau of Plant Industty” .cccc.tescsreseces-e Harrisburg, Pa. REE UREN, 2 Bo ED. ccs cocssccsccweoes=< U. S. Bureau of Entomology ................-.+- Washington, D. C. TINGS aN Ee Wie cos saccenasctcaccsansccse-s Cornell’ (University) :28. 2:5. 2s Ithaca, N. Y- POLAE SON STD WW oA. . ia stsscccscrepsteeeteecs University, Of WOrante <.:-cesccscoscceccreee-t acer Toronto, Ont. UO CHE REN Tr CA. 5. .ccccessnocees University of \Oolorad ojacc-cr- © te mn ee sole er em DONT THE CANADIAN ENTOMOLOGIST. II taken by me at those stations. In the rainy season, May to August, there is probably good collecting to be had here, at least 1 was so told by my landlady, Mrs. C. G. McKinney, who for years has collected butterflies and Orthoptera for northern supply houses. At that season, however, mosquitoes are at their best, and they were bad enough for me in March. I left Chokoloskee for Ft. Myers on March 18, by a little freight steamer which plies between the two ports. Had one afternoon’s collecting at Marco, where we passed the night, and part of the next one at the extinct pond at Ft. Myers. It was on this last afternoon at the pond that | took the second known specimen of my Pachydrus princeps. 1 did not recognize it at the time, else | might have been there yet, searching for others. The next morning I took the irain for Tampa and from there to Dunedin by automobile bus, arriving at 4 P.M. Dicaelus quadratus Lec.2—A single female, 25 mm. in length was taken March 6 beneath an old boat on the margin of the extinct pond at Ft. Myers. It 1s the same as a species from St. Petersburgh, identified for me by Frederic Blanchard as D. carinatus Dej. and recorded by me under that name.? I did not at that time have a copy of LeConte’s description of quadratus available, but with it now in hand there is no doubt that the two specimens are his species, which he states is .g6 of an inch in length. Horn, in his synoptical table,* separates quadratus from carinatus only by the humeral carina being “moderately elevated and acute near the base only” in quadratus and “very long and more elevated, acute in the entire length” for carinatus. In his bibliography he gives the length of quadratus as 25 mm., and of carinatus as 20 mm. ‘The question arises, may not these two nominal species represent the different sexes of one? If so, it would have to bear Dejean’s name. Dicaelus subtropicus Casey —The types of this species? were from Palm Beach, Fla. A single specimen was taken on February 9 beneath a chunk on Hog Island, opposite Dunedin. The species of Badister with unspotted elytra form a difficult group to separate satisfactorily with words. The original descriptions of Leconte are conflicting in a number of instances with his later keys® and as a consequence the species are badly confused in most collections. Three species of this group have been taken by me in Florida, one of which appears to be undescribed. Badister flavipes Lec—One specimen March 18 from the extinct pond at Ft. Myers. In the original description the intervals are said to be convex, whereas in the keys of LeConte it is included under division with intervals flat. In the specimens at hand, from Little River and Ft. Myers, the three innermost intervals are subconvex, the outer ones flat. 2In the notes and descriptions which follow, the sequence and nomenclature is that of Leng’s new “Catalogue of the Coleoptera of America north of Mexico.” Where’ the generic name used by him is different from that heretofore in common use the old name in parenthesis follows the new, e. g. Pseudamphasia (Anisodactylus ) sericea Harris. 3Can. Ent., xlvi, 1914, 63. 4Bull. Brook, Ent. Soc.. iii, 1880, 51. oMemoirs iv, 1913, 151. Trans. Amer. Ent. Soc., viii, 1880, 165: Bw'l, Bresk. Ent. Soc.. v, 1882, 7. 12 ; THE CANADIAN ENTOMOLOGIST. Badister seclusus sp. nov. Elongate-oval. Black, shining, the elytra and under surface strongly iridescent; narrow margins of thorax and elytra brownish-piceous; antennae piceous, the two basal joints paler; palpi and legs dull brownish-yellow, head as wide as base of thorax, finely alutaceous, impunctate, its front portion dis- tinctly declivent and concave with prominent raised margins; eyes very large and prominent; antennae nearly half as long as body, the third joint more than twice as long as second, slightly shorter than fourth, joints 4 to Ii very stender, more than four times as long as broad. Thorax short, widest at apical third, the sides thence oblique and distinctly converging to base, which is but two-thirds as wide as apex; side margins narrow to behind the middle, then gradually widen- ing and reflexed to base; hind angles obtuse, not rounded; median line deep, entire; basal impressions narrow, deep. Elytra at base one-third wider than base of thorax; humeri broadly rounded, sides straight and parallel from basal fourth to apical fifth, then broadly rounded into the obtuse apex; striae deep, intervals subconvex, the second with two large dorsal punctures on its inner margin, the first at middle, the other at apical fourth. Length 4.8 mm. Dunedin, Fla.. March to—April 19. ‘T'wo specimens taken by sweeping ferns in a dense damp hammock. Evidently allied to flavicornis Casey, de- scribed? from Iowa but much smaller and with dark antennae. The basal side margins of thorax are much more strongly widened and reflexed than in reflexus, the hind angles more distinct. It is possible that this is the species listed as B. micans Lec. by Schwarz, and by Leng, but it is a much smaller species with very different form of thorax from what I have as micans from Indiana, which was compared with LeConte’s labelled type. As pointed out by Casey, loc. cit., the original description of micans calls for a species 4% lines (g mm.). Badister reflexus Lec—Four specimens from the pond at Ft. Myers; one from Tallahasse. Leng records it® only from Suwanee. The Florida specimens agree with those from Indiana in having the hind angles “very obtuse and rounded,” as stated by LeConte in his original description, whereas in his key they are mentioned as “obtuse, not rounded.” Pseudamphasia (Anisodactylus) sericea (Harris)—This common northern Carabid has not heretofore been reported from Florida, though it is known irom Louisiana. ‘Two specimens were taken from beneath debris on the shore of Lake Okeechobee near Moore Haven on March 2, 1918. Casey® has re- cently erected for it the genus Pseudamphasia. Pronoterus semipunctatus ‘(Lec.)—From the muck about the Pontederia roots in the pond at Ft. Myers I took three specimens of a small Dytiscid which I was unable to identify, even as to genus, with the literature available. Think- ing that it perhaps might be a West Indian form, I sent a specimen to A. J. Mutchler of the American Museum of Natural History. He replied that it was not represented in the Museum collection either from the United States or West Indies, and suggested that I refer it to H. C. Fall, who has been making a recent 7TMemoirs, ix, 1920, 20S. 8Bull. Amer. Mus. Nat. Hist., xxxiv, 1915, 581. 9Memoirs v, 1914, 195. THI CANADIAN ENTOMOLOGIST. 13 study of the smaller Dytiscidae. This I did, and Mr. Fall reported that: “It seems almost surely to be the rare Canthydrus semipunctatus (Lec.) described from Michigan!®. It is also-probably Pronoterus punctipennis Sharp, described from Brazil! On comparing your specimen with LeConte’s unique type in the Cambridge Museum I find that it differs only in being a little smaller, with some- what darker elytra and with the posterior angles of the hind coxae a little more blunt. I cannot feel so sure that Sharp’s species is the same, but the short de- scription is perfectly characteristic so far as it goes. It is not a Canthydrus, but must be referred to Sharp’s genus Pronoterus and, LeConte’s name being the elder, must be known as Pronoterus semipunctatus (Lec.). I do not know that LeConte’s specimen has ever been duplicated in this country, so your find is one of great interest. Truly a remarkable distribution if the Michigan, Florida and Brazilian specimens are all one thing!” Pachydrus (Coelambus) princeps (Blatch.)—The second known specimen was taken March 19 from amidst the decaying stems of pickerel weed in the extinct pond at Ft. Myers. The unique type was from the east shore of Lake Okeechobee. It was described!! as a Coclambus, but Fall states!* that it belongs to Pachydrus, a tropical genus, hitherto unrepresented in this country. Celina slossoni Mutch—One specimen, April 1, from a mass of water weeds in a small pond near Dunedin, known heretofore only from Sanford, Enterprise and Lake Worth, on or near the east coast. Derallus altus (Lec.)—Three specimens were taken from the debris of the extinct pond at Fort Myers. The only other Florida record is that of mine from Dunedin?*. Helobata (Helopeltis) larvalis (Horn.)—Two specimens were secured from the under side of the decaying leaves of pickerel weed at the Ft. Myers pond. They clung to their cover much as did a small mollusk of the genus An- cylus which was frequent on the leaves. | While the beetle has been taken at several stations in Florida, the only definite one hitherto recorded is Sarasota, where I found a single individual in 1911. Bacanius subdepressus sp. nov. Broadly oval, subdepressed. Black, shining; femora piceous, antennae, tibiae and tarsi dark reddish brown; the globular antennal club much paler. Head two-thirds as wide as thorax. minutely and sparsely punctate. Thorax twice as wide as long, sides feebly curved, strongly margined, this margin con- tinuous and uninterrupted to tips of elytra; disk, finely, evenly and rather sparsely punctate, base with a single transverse row of smaller punctures. Elytra as wide at base as, and about two-thirds longer than, thorax, without marginal carine or discal striae; sparsely, rather coarsely punctate, the punctures on basal half in _ part aciculate or substrigose. Pygidium, very minutely punctate. Prosternal process broad, one-half longer than wide, striate each side, minutely punctate, truncate at tip. Metasternum very broad, both it and abdomen very minutely and sparsely punctate. Length .8—1 mm. 10Proc, Amer. Phil. Soc.. xvii, 1878, 595, 11Can. Ent., xlvi, 1914, 64. 12The N. Amer. species cf Coelambus, 1919, p. 1. 13Bull. Amer. Mus, Nat. Hist. xli, 520. I4 THE CANADIAN ENTOMOLOGIST. Frequent and gregarious, November to April, about Dunedin, beneath the bark of dead water oak and dead white bay; also taken beneath cow dung and by sifting in damp mucky places. Much less convex than any of our other de- scribed species. (To be Continued.) NEW SPECIES OF CANADIAN SYRPHIDAHE, (DIPTERA) Pt. EF. BY C. HOWARD CURRAN, Orillia, Ont. Cynorhina robusta, new species Thorax and scutellum moderately long, pale yellow pilose; abdomen black pilose except the immediate basal corners which bear yellow pile; head brown and black pilose; face chiefly piceous, but yellow above. Length 11 mm. @. Face piceous, immediately below the antennae, more so at the sides, yellow, the cheeks black; face thinly silvery pollinose, the side inargins sparsely whitish pilose; in profile the sub-keel-shaped face is slightly produced below the middle indicating a long tubercle. Antennae black, third joint circular and reddish brown in color, the base below reddish; arista black. Front shining black, somewhat narrowed above; antennal process narrowly reddish apically. Pile of the front black; under the eyes yellowish, on the lower half of the occiput brown, black on the upper half, moderately long below. Posterior orbits narrowly grayish white pollinose. Thorax shining deep blue-black; mesopleurae margined with reddish except below. Dorsum brassy, and clothed with rather long pate yellow pile; pleurae bare except on the meso and sternopleurae; scutellum similar in color and pile to dorsum. Abdomen wholly shining black, with a strong purplish reflection, wholly short black pilose except the basal angles which bear longer yellowish pile. First two ventral segments yellow apically at the sides. Legs blackish, short black pilose, longer on the femora; femora tipped with yellow; bases and ends of the tibiae yellow or yellowish; first three joints of the anterior four and second and third of the hind tarsi, yellow. Wings moderately brownish, less so outwardly, their bases very con- spicuously yellow; stigma brownish, but not readily discerned. Squamae whit- ish yellow, with similar colored fringe. Halteres yellow. Holotype, 2, British Columbia, in the Canadian National Collection, Ot- tawa. A robust, conspicuous species resembling Criorhina, best characterized by the color of the face and the pile, which is longer and denser than usual. Cynorhinella, new genus Face considerably produced downwards, tuberculate; side margins distinct; eyes contiguous; antennae short, third joint roundish; thorax longer than broad, without bristles; abdomen slender, twice as long as the thorax, tapering in the male; femora all somewhat swollen, the hind ones considerably so and arcuate, at the end below with an angular projection exteriorly, as in THE CANADIAN ENTOMOLOGIST. ; 15 Tropidea, a smaller one anteriorly; hind tibiae a little arcuate, not ending in a spur. Wings as in Cynorhina. Genotype, C. canadensis, new species. I am unable to place the following specimen in any genus known to me, and it traces out to Cynorhina in Williston’s manual, and apparently comes closest to this genus but the thickened, arcuate hind femora with the projection apically, and the more distinct facial side margins separate it. It is related to Chilosia and Chrysochlamys by the last mentioned character, but there is no semblance of bristles and the shape of the abdomen is distinctive. Superficially it moderately resembles a Brachypalpus but the facial shape and tubercle at once preclude it from that genus. ; Cynorhinella canadensis, new species Length 10mm. Male. Face chestnut brown, concave below the antennae with a prominent rounded tubercle about the middle, below which it is slightly produced to the not prominent oral margin; side margins well defined, as in Chilosia, the facial slopes with fine whitish pollen, the side margins with sparse whitish pile; cheeks and frontal triangle shining, concolorous with the face; vertical triangle brown, the sides of the triangle about equal, with brown pile; occiput shining chestnut, with whitish pile below and brownish above. Thorax shining blueblack, the dorsum with yellow pile, which is intermixed with black on the middle, and black pile on the borders; pleurae yellowish brown, with yel- lowish pile, the pile black above. Scutellum concolorous with dorsum, with slightly longer black pile. Abdomen narrow, and gradually narrowing after the second segment, in color shining blue-black, the posterior margins of the second and third segments a little more blackish on the median two-thirds; hypopygium black. Pile of abdomen yellowish on basal angles, becoming white en the hypopygium, and black on the ends of the second and third segments. Legs chestnut brown. Wings distinctly luteous; stigma yellowish. Squamae and halteres white. Holotype, 6, Inverness, B.C., July, 1910, (J. H. Keen), in the Canadian National Collection, Ottawa. Mallota columbiae, new species Eyes bare; abdomen wholly black pilose; wings with a brown spot; thorax densely yellowish pilose. Distinguished from cimbiciformis by the shape of the angulation of the third vein, from sackeni by the open marginal cell. Length 14 mm. Female. Face shining black, the sides covered with grayish yellow pollen, forming a complete band below the antennae. Front shining black, the sides with yellow pollen; pile of the head black, except a few whitish. hairs on the cheeks; below the eyes there is a very distinct, triangu- far rust-colored spot. Antennae brown, third joint more reddish, large, broader than long; arista reddish. Thorax shining greenish black; anteriorly, except two narrow sub-median stripes, yellowish pollinose, in some lights a broader inter- rupted more shining stripe laterally. Scutellum light yellow. Pile of thorax and scutellum light yellow, the humeri and pleurae below with blackish hairs. Abdomen shining black, black pilose, but the sides of the second segment nar- rowly, with yellow hairs. Femora black, with black pile, tibiae more brownish, 16 THE CANADIAN ENTOMOLOGIST. tarsi reddish; tips of the femora, narrow base of the hind and broad bases of the anterior four tibiae, yellowish red; pile of the tibiae very short, brownish. Wings almost hyaline, with a brown cloud at the middle. Third vein with the angulation more V-shaped than U-shaped. Holotype, 2, Penticton, B.C., June 5, 1919, (R. C. Treherne), in the Canadian National Collection, Ottawa. This species comes close to cimbiciformis, but is at once distinguished by the clouded wings, wing venation and facial profile. M. sackeni has the mar- ginal cell closed. No other species with the abdomen practically entirely black pilose have been described; there are very few yey hairs on the sides of the second abdominal segment. Mallota diversipennis, new species Eyes bare; antennae luteous-reddish; third longitudinal vein with the loop V-shaped; wings clouded; marginal cell open; pile of abdomen rather sparse, mixed black and fulvous. Length, 15 mm. 9. Face black, shining, covered, except a broad median stripe and the cheeks, with yellowish gray pollen, and sparse, long reddish yel- low pile; front broad, the sides, more widely at the middle, with golden pollen, the pile rather sparse, reddish yellow, up the middle with black hairs, and chiefly black hairs across the ocellar triangle. Antennae luteous-reddish, shin- ing, (third joint missing). Posterior orbits with brownish pile, but more ful- vous below and at the vertex. Thorax black, a little shining, with reddish pile; humeri reddish, sec- tions of pleurae bordered with reddish and very slightly whitish pollinose; dor- sum with slight indications of pollen before the suture. Scutellum yellow with moderately long, fairly abundant pale yellow pile. Abdomen shining bluish black, with a purplish tint in some reflections; pile on first and second segments rather long, whitish, on the triangular median posterior half of second segment short, stiff, brown, elsewhere on tne abdomen shorter, fulvous, sparsely intermixed with brown, on the third segment with a broad posterior band of short brown pile. Femora brownish, hind ones more reddish; tibiae and tarsi yellowish red, the tibiae darker apically; pile of the anterior femora entirely black, rather leng posteriorly, on the middle ones brown, but longer reddish yellow poster- iorly, on the hind ones wholly reddish yellow; tibiae and tarsi with yellow pile; hind femora much thickened, the tibiae a little arcuate. Wings with a distinct brownish cloud across the middle beyond which the color is somewhat luteous, the base hyaline. Angulation of third longitudinal very acute and V-shaped. Holotype, 2, in the Canadian National Collection, Ottawa, bearing no label. It is probably a Canadian specimen. I cannot associate this species with any described. It comes nearest palmerae Jones but is distinct in the reddish antennae and color of the pile, that on the legs being especially distinctive. There is a short stump of vein into the first posterior cell from the tip of the V-shaped angulation. ——— ——— pace THE CANADIAN ENTOMOLOGIST. 17 Chilosia hunteri, new species Eyes pilose; antennae reddish yellow; arista bare; facial slopes without pile; thorax whitish or yellow. pilose, without spines, except a weak one on the mesopleura ; abdomen light pilose. Length 8 tog mm. Male. Face shining black, a little pubescent oppo- site the tubercle; side margins and below the antennae thinly silvery pollinose ; face almost straight from base of antennal prominence to the oral margin which is on a plane with the antennal base, the tubercle fairly prominent, on a plane with the tip of antennal prominence, a little concave between the an- tennal prominence and tubercle, and shortly, deeply concave below the tubercle; the lower edge of the short nose-shaped tubercle is on a plane with the lower eye margins; side margins and cheeks short yellowish pilose. Frontal triangle shining black; finely moderately punctured, usually with a narrow suica in the middle ; the polished broad W on the antennal prominence reddish or obscurely so; pile of the frontal triangle black, rarely mixed with yellow; posterior orbits narrowly silvery pollinose, with white pile; remainder of occiput thinly grayish pollinose. Antennae with the first two joints polished brownish red, the third bright reddish yellow, not large, sub-quadrate, a little rounded apically. Eyes short brownish yellow pilose. Thorax and scutellum shining metallic greenish black, with moderately short pale yellowish to yellow pile, a little deeper colored at the corners and usually with some black hairs intermixed here; there may be one to three weak bristles on the top of the mesopleura. Abdomen of the same metallic greenish black color, but not quite so shining, and a little more sparsely finely punctured; second segment with a goblet-shaped opaque spot widest posteriorly and poorly outlined; an abbre- viated, interrupted, basal opaque fascia on the third segment. Pile usually - all pale yellowish or yellow but there may be some black hairs towards the end of the second segment. Legs shining black, the trochanters obscurely reddish apically; femora tipped with reddish; tibiae with the basal quarter and a little less than the apical quarter reddish, the anterior ones a little more extensively reddish; tarsi all black, except that the base of the anterior four basitarsi may be reddish. The long hairs on the legs are yellow. the short ones black, except on the anterior of the front tibiae and the tarsal pads. Wings a little luteous, less so postero-apically; stigma and base of the wings brownish; 8 to Io short bristles on R,,;; tip of first posterior cell almost truncate, the last sec- tion of the fourth vein sinuous. Squamae slightly tinged with yellow, with white fringe of pile. Halteres reddish yellow, the end of the knob brown. Holotype, ¢, Teulon, Manitoba, May 17, 1920 (A. J. Hunter) in the Canadian National Collection, Ottawa. Paratypes, 6, Teulon, Man., May 14, 1920, (A. J. Hunter) in the col- lector’s collection; ¢, Teulon, May 17; ¢, Winnipeg, Man., May 7, 1910, (J. B. Wallis); in the writer’s collection; ¢, Winnipeg, May 7, 1910, (J. B. Wallis) in the collector’s collection. This species is evidently close to petulca Will. but may be known by the bare arista, absence of scutellar bristles and the color of the vestiture. From 18 THE CANADIAN ENTOMOLOGIST. baroni it is distinguished by its reddish antennae, absence of spines and the color of the vestiture. I take great pleasure in naming this species in honor of Dr. A. J. Hunter, who has sent me many fine specimens of Syrphidae, and whose ef- forts have added largely to our knowledge of the Syrphid fauna of Manitoba. I place a female collected by Dr. Hunter at Teulon on May 14, 1920, here with some doubt as it appears rather darker. Female. Face shining black, a little more prominent than in the male, as the oral tip is as prominent as the antennal base, the tubercle more promin- ent; third antennal joint larger, twice as broad as the second joint. Front brassy in the middle, the sides smoother, black; a slender longitudinal median shining darker stripe which is more or less impressed, and a transverse depres- sion above the antennae; pile blackish above the antennae and at the ocelli, elsewhere fulvous; occiput dull, thinly grayish yellow pollinose, the pile whitish below, cinereous above. Eyes short fulvous pilose. Thorax shining slightly brassy black, with a median rather broad vitta and a broad one sub-medianly on each side, less shining and darker. The pile on the thorax and scutellum is very short fulvous, but appears to be darker on the darker vittae, and on the immediate sides of the dorsum there are a few longer bristle-like black hairs and the pile on the end of the scutellum is partly black and subappressed. Abdomen shining black with a brassy reflection, the disc of the second segment deep black. The pile is very short subappressed fulvous, appearing darker on the third and base of the fourth segment on the disc in some lights; on the base of the abdomen and anterior angles of the segments it is longer, on the fifth segment with some black hairs apically. Legs as in the male but the tarsi brownish, the first joint of the anterior four tarsi reddish. Squamae white with a yellow fringe and pale yellow pile. Halteres yellowish red. Myiolepta lunulata Bigot. Bigot, (Ann Soc. Ent. France, 1884, page 537) described a specimen of Myiolepta from Oregon, giving it the specific name lunulata. As is the case with most of Bigot’s descriptions the insect is not recognizable, and as a re- sult Williston, (Syn. N. Am. Syrph., 1886) placed lunulatus as a synonym of varipes Loew. In the Museum of the California Academy of Sciences is a specimen of Myiolepta which is moderately like varipes, but there are certain differences which I can only regard as specific, and hence give a description of the specimen using Bigot’s name lunulatus rather than a new one. The specimen was collected at Huntington Lake, Fresno Co., California, at an altitude of 7,000 ft. by Mrs. F. P. Van Duzee and is a male. Abdominal coloration in the male very much like the female of M. varipes; pile of abdomen depressed, mostly black; antennae dirty brownish yellow ; wings clouded only across the middle; arista blackish. Male. Length 7 mm. Swollen antennal base, cheeks and face from just above the tubercle to the mouth edge scarcely wider than the tubercle, deep shining black, the face elsewhere obscured by grayish yellow pollen. In pro- ae THE CANADIAN ENTOMOLOGIST. 19 file the face is very deeply concave; from the antennal prominence to the deepest part of the cavity it is almost straight, thence it is straight to the an- terior oral margin, which does not project quite as much as the antennal prom- inence; the tubercle, situated in the middle of the lower straight portion, is mod- erately large, more rounded above, sub-pointed on its lower portion and almost at a right angle to the lower facial plane. Frontal triangle shining black, the sides narrowly grayish yellow pollinose. Vertical triangle black. Pile sparse, whitish, on the face restricted to the side margins. Thorax and scutellum shining deep black; in front with an arch of grayish pollen extending between the humeri; pile short, yellow, subappressed ; on the pleurae more erect, lighter. Scutellum margined with sparsely placed short black hairs. Abdomen shining black; second segment except the sides and the base of the third segment medially, more opaque. First segment grayish pollinose. Second segment with a half-crescent-shaped yellow spot, extending along the latero-irontal margin a short distance, then curving back; behind and laterally to lunule the ground color is inclined to be lighter fading to black. Abdominal pile short, subappressed, on the abdominal basal angles, on the lighter areas and the basal triangles of the third segment, longer, whitish, more erect. Legs black; bases of the tibiae piceous; hind tarsi and middle tarsi yellowish basally. All the femora thickened and bearing spines below. Hind tibiae without a triangular protuberance below. Wings subhyaline, darkened on the middle anteriorly. Stigma luteous, occupying the basal two-thirds of the cell. Differs from varipes in that the wings are not clouded beyond the middle ; pile mostly black on the abdomen; in the male of varipes the sides of the second abdominal segment are yellow; the face in /unulata is more produced and below the tubercle it is not receding to the oral margin as in varipes, but is continued forward. NEW SPECIES OF THE SYRPHID GENUS CHILOSIA FROM CANADA (DIPTERA) BY C. HOWARD CURRAN, Orillia, Ont. Chilosia sensua, new species. Eyes bare; arista bare; wings strongly tinged with brownish yellow; scutellum without bristles; abdomen partly opaque. Male. Length 7 mm. Face and front shining black, the former thinly grayish pollinose across below the antennae, pile of the side margins short, sparse, whitish, of the frontal and vertical triangles, black, of the posterior orbits, whitish below, yellow above. Eyes bare. Vertical triangle short, eyes touching for about the length of the vertical triangle. Frontal triangle large, a little prominent, with a metallic blue reflection in the middle, densely finely punctured ; in the middle, when viewed from in front with an elongate triangular depression, its narrow base resting upon the antennal arch, its upper point almost reaching the juncture of the eyes. First antennal joint shining black, second piceous or brownish, third reddish, its end and upper portion more or less blackish, but 20 THE CANADIAN ENTOMOLOGIST. the ground color considerably obscured by whitish pubescence, in shape broader than long, flattened above, its upper apex more acutely rounded than the lower; arista black, bare, considerably thickened basally for about one-third its length (not as much as in C. crassiseta of Europe), then suddenly thinned. Thorax and scutellum shining greenish black, the dorsum with a slight brassy reflection, covered with moderately short fulvous pile, but a stripe of black pile from the humeri to the base of the wings, and some black hairs about the postalar callosities. Abdomen metallic greenish black; first segment with an opaque area on each side; second segment opaque black, the sides shining, the lateral ends of the opaque only very slightly concave and a little broader posteriorly; the opaque on the third segment is a little narrower than that on the second, does not quite reach the posterior margin and is not at all concave laterally. Pile of abdomen wholly fulvous. Legs black, tips of the femora, bases of the tibiae and the apices of the front four tibiae reddish; basal tarsal joints brownish. Wings distinctly luteous, more clouded across the middle; stigma luteous; the first posterior cell ends in an acute angle. Squamae whitish yellow fringed with pale yellow pile. Halteres reddish. Holotype, ¢, Orillia, Ontario, May 5, 1921 (Curran), in the writer’s collection. This species is related to crassiseta Becker of Europe, but the arista is not so much enlarged; differs from capillata in black pile of head, truncate shape of opaque of the abdomen and lighter colored legs, the face almost similar in profile; from comosa in the shape of the opaque markings and brownish wings; from nigripennis and versipellis in having yellow pile on thorax, etc.; from parva in the dark legs; from ontario in smaller size, different shaped antennae, arista, etc. THE FAMILY POSITION OF PLATYPREPIA AND OTHER NOTES. (LEPID.) BY HARRISON G. DYAR, A.M., PH.D., U. S. National Museum, Washington, D. C. Some remarks by Dr. McDunnough seem to call for a little elucidation (Can. Ent., LIII, 167, 1921). I am quoted as claiming that Platyprepia be- longs to the Hypsidae. This claim was not intended as original, as Dr. Mc- Dunnough’s remarks seem to imply, but in following the established literature of the group it is well known that in Sir George Hampson’s classic work, Platyprepia is omitted from the Arctiidae, together with Callimorpha (in the Ed. Note.—The above article serves to elucidate Dr. Dyar’s rather negative views in regard to the family position of Platyprepia but still leaves the correct posi- tion of this genus in doubt. ‘The fact remains that the anastomosis of veins 7 and 8 of secondaries in P. guttata, a so-called Hypsid, is as long as, or even longer than that found in Arctia caia, the typical Arctiid. Author's Note.—In estimating the length of the anastomosis, I do not count from the base of the wing to the point where veins 7 and 8 separate, which appears to be Dr. McDunnough’s standard, but from the point where veins 7 and 8 fuse to where they separate again, In Platyprepia, these veins are free at the base, anastomose for about — 5 mm., then separate. In Arctid. they are united to the base, making the length of the anastomosis about 7mm, On this basis a more positive distinction can be made, and the reference of Platyprepia the Hypsidae retained, THE CANADIAN ENTOMOLOGIST. 21 European sense) and the groups which we used to call Pericopidae, Nyctemer- idae and Hypsidae. These we expect him to treat under the family Hypsi- dae (Callimorphidae), except that his labors unfortunately terminated with the Noctuidae. I do not recall any statement by Hampson that Platyprepia be- longs to the Hypsidac; but this seemed the only possible inference from his work that had appeared. After 1902 I regarded it as negatively established, and hence my remark which Dr. McDunnough refers to was briefly made. It is also true that Sir George defines the family Hypsidae by having vein 8 of the hind wings connected with the cell by a bar. This can be verified by any of the Hypsa proper, and the definition remains unchanged in his latest publication (Nov. Zool., xxv, 389, 1918). However, in Callimorpha, the Nyctemeridae and Pericopidae the bar becomes a short anastomosis, as tacitly admitted by Hampson in his Moths of India (1894) where he places Nyctemera in the Arctiidae. The definition of the family thus becomes con- fused; but I have followed Sir George in his classification. Therefore Dr. McDunnough’s remark that he would retain Platyprepia in “its present position in the Arctiidae’ seems somewhat inappropriate, since Platyprepia has been omitted from the Arctiidae for the last twenty years by the most authoritative student of the world fauna, and not again restored by him in his latest reference (Cat. Lep. Phal. B. M., Suppl. vol. ii, 1920). If Dr. McDunnough wishes to differ from Hampson, which of course he has the right to do, the question of Platyprepia widens to include: all of the Pericopidae and Nyctemeridae, for there is no difference that I can perceive in the venation. The anastomosis is shorter in these forms than in the Arctiidae in general, and if a more or less short anastomosis can be called a bar, it is possible to follow Hampson’s classi- fication, and this I suppose it is better to do if possible. Uniformity in no- menclature is so desirable that we should stretch a point to conform, if it can be -done. For these reasons I would let Platyprepia remain in the Hypsidae instead of transferring it to the Arctiidae as Dr. McDunnough proposes. Dr. McDunnough further refers to a similarity of larvae and male geni- talia; but this similarity probably runs through all the groups mentioned. In the same article Dr. McDunnough refers the species alpina Quensel to Arctia after showing the generic separation from Hyphoraia. In this he agrees with Hampson, who made the same reference and separation pre- viously (Cat. Lep. Phal. B. M., Suppl. ii, 500, 1920). Hampson does not record A. alpina from America; but the European Arctic Fauna is the same ay the American Arctic, apparently entirely, as far as these forms are con- cerned. THE ENTOMOLOGICAL SOCIETY OF ONTARIO—ANNUAL MEETING The fifty-eighth Annual Meeting of the Entomological Society of Ontario was held at the University of Toronto during the week of December the twenty- eighth. The meeting was held at this time in order to afford our members an opportunity of meeting with the members of the Entomological Society of Amer- ica and of the American Association of Economic Entomologists. 22 THE CANADIAN ENTOMOLOGIST. Among the members present were Dr. C. J. S. Bethune, Toronto, Ontario; Mr. J. D. Evans, ‘Trenton, Ontario; Prof. J. H. Comstock, Ithaca, NY.; Dr. I,--O. Heward, Washington, D.C.; Dr. E. P. Felt, Albany, N.¥:; Prot. Me Walker, Dr. W. A. Clemens, Dr. Craigie, Mr. Bigelow and Miss Norma Ford, Toronto University; Messrs. A. Gibson, Dr. Swaine, L. S. McLaine, R. C. Treherne, H. G. Crawford and F. C. Craighead, Dominion Entomological Branch, Ottawa; Profs. L. Caesar and A. W. Baker and Messrs. G. J. Spencer and W.: G. Garlick, O. A. College, Guelph, Ont.; Miss Edna Mosher, Albuquerque, N. M.; Father Leopold, La Trappe, Ont.; Prof. W. H. Brittain; Truro, N.S.;.Mr. F. J. A. Morris, Peterborough, Ont.; Dr. J..D. Detwiler, Western University, Lon- don, Ont.; Mr. C. H. Curran, Orillia, Ont.; Mr. W. E. Biggar, Hamilton, Ont. ; Prof. A. V. Mitchener, M.A. College, W edges Man.; Dr. Matheson and Mr. H. C. Huckett, Cornell University, Ithaca, N.Y.; Drs..S. Hadwin and A. C. Baker, Washington, D.C.; and the following officers of the Dominion Entomo- logical Branch :—Messrs. G. E. Sanders, Annapolis Royal, N.S.; J. D. Tothill, Frederickton, N.B.; C. E. Petch, Hemmingford, Ont.; W. A. Ross, Vineland Station, Ont.; H. F. Hudson, Strathroy,-Ont.; Norman ‘Criddle, Treesbank, Man.; E. H. Strickland, Lethbridge, Alta. ;-and W. Downes, Victoria, B.C. The meetings were also well attended by members of the Entomological So- ciety of America, the American Association of Economic Entomologists and others. On Wednesday afternoon a meeting was held with the Entomological Society of America in Room 10, Medical building. The following papers were contributed by members of the two societies. Algonquin Days,—F. J. A. Morris, Peterborough, Ont. Hatching in Three Species of Neuroptera——Roger C. Smith, Kansas State Agricultural Society. Ecdysis in Tmetocera Ocellana.—S. W. Frost, Arendtsville, Pa. Cocoon Spinning by Species of Bucculatrix—O. A. Johannsen, Cornell University. The Ventral Pro-Thoracic Gland of the Red-Humped Apple Caterpillar (Schizura concinna)—J. D. Detwiler, Western University. Observations on a New Species of Chrysops ‘rom Central New York.—’ Raymond C. Shannon, Cornell University. Are There Two Species of the Oyster-Shell Scale?—Grace H. Griswold, Cornell University. A Classification of the Larvae of Tenthredinoidea——H. Yuasa, University of Illinois. The Phylogeny of the Gall Mites and a New Classification of the Suborder United States National Prostigmata of the Order / Museum. The Syrphid Genera Haminensahannena and picige in ge ki Cc Howard Curran, Orillia, Ontario. Ai, Taxonomic Results from a Study of the Genitalia of Male S jrphldel C. L. Metcalf, University of Illinois. omit (Ol we THE CANADIAN ENTOMOLOGIST. 23 Report of the Lepidoptera of the Cornell Expedition of 1919-1920.—Wm. ‘'T. M. Forbes, Cornell University. An Extreme Case of Delayed Fall Emergence of Hessian Fly (Phytophaga destructor )—W. H. Larrimer, United States Bureau of Entomology. Importance of Insects in the Food of the Brook Trout.—W. A. Clemens, University of Toronto. The Effect of Vitamines on the Growth of Ephestia Kuehniella in Wheat Flour.—Charles H. Richardson. United States Bureau of Entomology. On Friday afternoon the Society met with the American Association of Economic Entomologists when the following programme was delivered. One Year of the Crop Protection Institute—W. C. O’Kane, Durham, N.H. Poisoned Molasses for the Destruction of Noctuid Moths.—E. H. Strick- Jand, Ottawa, Canada. The Western Wheat Stem Sawfly in Canada.—Norman Criddle, Trees- bank, Manitoba. Progress in Hessian Fly Control—H. A. Gossard, Wooster, Ohio, and ‘'T. H. Parks, Columbus, Ohio. European Corn Borer: Life History in Ontario.—H. G. Crawford, Ottawa, Canada. European Corn Borer: Present Distribution in Ontario.—L. $. McLaine, . Ottawa, Canada. European Corn Borer: Control Under Ontario Conditions.—G. J. Spencer, Guelph, Ontario, Canada. The Corn Borer Problem in New York State.—E. P. Felt, Albany, N.Y. Chemotropism of Chinch Bug.—H. Yuasa, Urbana, II. Observations on Insects Attacking Sorghum.—Wm. P. Hayes, Manhattan, Kansas. The Onion Maggot in British Columbia Under Irrigated Conditions.— R. C. Treherne, Ottawa, Canada. The Cabbage Root Maggot.—L,. Caesar, Guelph, Canada. A Forest Insect Survey from the Air.—J. M. Swaine, Ottawa, Canada. Forest Sample Plot Studies in a Spruce Budworm Outbreak.—F. C. Craig- head, Ottawa, Canada. The Life History, Habits and Injuries of the Maple Case-Bearer—Glenn W. Herrick, Ithaca, N.Y. On Friday evening an entomologists’ dinner was held at the Prince George Hotel under the auspices of the American Association of Economic Entomolo- gists. Many members of our society accepted the kind invitation of this society to be present. The business meeting was held on Saturday morning. Considerable dis- cussion in regard to the financial condition of the society took place. The fol- lowing officers were elected for the ensuing year: President—Mr. F. J. A. Morris, Peterborough. Vice-President—Dr. J. M. Swaine, Entomological Branch, Ottawa. Secretary-Treasurer—Prof. A. W. Baker, O.A. College, Guelph. 24 THE CANADIAN ENTOMOLOGIST. Curator and Librarian—Mr. G. J. Spencer, O.A. College, Guelph. Editor—Dr. J. McDunnough, Entomological Branch, Ottawa. Auditors—Prof. L. Caesar and Mr. J. A. Flock. The directors were re-elected save that Dr. J. D. Detwiler was appointed. director in division No. 5. THE ENTOMOLOGICAL SOCIETY OF AMERICA At the very successful annual meeting of the above society, held in Toronto during the week of December 28th, the following officers for 1922 were elected. PrESIDENT—Arthur Gibson, Dominion Entomologist, Ottawa, Canada. First VicE-PrEsSIDENT—Dr. W. A. Riley, University of Minnesota, St. Paul. SEeconp VicE-PREsmDENT—Professor R. A. Cooley, University of Montana, Bozeman, Mont. SECRETARY-TREASURER—Dr. C. L. Metcalf, University of Illinois, Urbana, III. ADDITIONAL MEMBERS OF THE EXECUTIVE COMMITTEE: Dr. J. M. Aldrich, United States National Museum, Washington. Mr. Wm. T. Davis, New Brighton, N.Y. Dr. E. M. Walker, University of Toronto, Toronto, Ontario. Dr. O. A. Johannsen, Cornell University, Ithaca, N.Y. MANAGING EDITOR OF THE ANNALS—Dr. Herbert Osborn, Ohio State University, Columbus. EprtortAL BoarD: Dr. W. S. Marshall, University of Wisconsin, Madison, Wisconsin. Dr. Vernon L. Kellogg, National Research Council, Washington. Dr. F. E. Lutz, American Museum of Natural History, New York. Dr. Wm. M. Wheeler, Bussey Institution, Boston 30, Mass. Dr. E. M. Walker, University of Toronto, Toronto, Ontario. ‘Dr. S. A. Forbes, University of Illinois, Urbana, II]. Dr. A. D. Hopkins, Bureau of Entomology, Washington, D.C. Prof. A. L. Lovett, Oregon Agricultural College, Corvallis, Ore. Dr. Frederick C. Muir, H.S.P.A. Experimental Station, Hawaii. Assistant Manacine Eprror—Dr. C. H. Kennedy, Ohio State University, Columbus. A.W.B. JOHN MACOUN MEMORIAL VOLUME. The Ottawa Field-Naturalists’ Club have issued a prospectus of the pro- posed autobiography of the late Professor J. Macoun, Canadian Explorer and Naturalist, who occupied the position of Director and Naturalist to the Geological Survey of Canada. It is expected that a sufficient number of subscriptions for this Memorial Volume will be received and that the same will be published and ready for mailing in the autumn of 1922. It is expected that the manuscript will make a volume of between 300 and 400 pages. The Treasurer of the Committee, Mr. Arthur Gibson, Dominion Entomologist, Birks Building, Ottawa, is receiving subscriptions for the price of the Volume, namely $3.00. a ~~ Che Canadian Cutomolonist Vor. LIV. ORILLIA, FEBRUARY, 1922. No. 2. POPULAR AND PRACTICAL ENTOMOLOGY NotEes ON SoME INsEcts AFFECTING NATIVE CoTroNnwoops BY WALTER CARTER, Dominion Entomological Laboratory, Lethbridge, Alta. The cottonwood grows to a considerable size in the river bottoms in Alberta. It has a rapid growth, and this, together with the shade it affords renders it very valuable as an ornamental tree on the prairies. Trees planted ten and eleven years ago on the Experimental Farm at Lethbridge are now Io to 15 inches in diameter. A feature of the trees’ growth, which led to the fol- lowing observations, is the cracking of the old bark, especially around the bases of the branches, and a constant exudation of sap. This is seasonal and ap- parently of not much consequence to the tree, though it should be mentioned in this connection that all the trees referred to are growing under irrigated conditions. On June 28th, 1921. attention was drawn to large unsightly masses of faecal matter in the cracks of the bark, and on examining these, colonies of a noctuid larva were disclosed, apparently feeding on the bark. Examination of all the cottonwoods in the vicinity showed these colonies to be present in the cracks or in pruning wounds where the sap was exuding. The larvae were closely packed together, were entirely concealed, and neg- atively phototropic. They were unable to craw! on the smoother surface of the tree, and once removed from the moist strands of old bark were unable to return. Much of the fresh faecal matter was light green, which suggested that living tissues were being fed upon. Fresh intestinal contents showed cortical and xylem elements present which had all the usual appearances of living plant cells. It is apparent therefore,.that the larvae do not confine their attentions to old bark, but feed on living tissues—apparently the scoring noticed on the new bark is a result of their activities. Specimens reared in the laboratory were fed on pieces of bark taken from the neighborhood of the colonies. | About fourteen pupated, and several other pupae were obtained from the cottonwoods. While looking for these latter, we found that numerous other forms of life inhabited these cracks in the bark. Mites, weevils, spiders, and many forms of dipterous larvae were abundant, as well as the pupe of more than one species of noctuid moth. Some of these latter proved to be Rhynchagrotis placida Grt. 26 THE CANADIAN ENTOMOLOGIST. and two larger pupz were obtained from which later a Catocala species emerged. The larvae of the last mentioned were also found on the tree and two individuals were found pupating under the bark. The pupe of the principal species mentioned in this article were found in the trees on July Ist, in cocoons made of old strands of bark intermingled with silk. Specimens reared indoors pupated July roth and 11th. These speci-. mens emerged from the 30th of July to the 5th of August and were determined by Dr. McDunnough as probably Ufeus plicatus Grt. Control:—The question of the control of the Ufeus species was given attention during the summer. Of all the colonies examined, over 80 per cent. failed to mature through natural causes. Apantcles sp. emerged on July toth, from a mass of cocoons attached to a dead larva. Such masses were present on most of the colonies. Tachinid larvae were taken from a diseased specimen during the examination of intestinal contents, and a tachinid puparium was obtained from one of the reared specimens. A disease, with symptoms very much like flacherie, accounted for many of the colonies, wiping them out completely. Where the sap ceased to exude before the colony was mature, the bark dried out and the colony died. Mention might also be made of the fact that of five R. placida pupz ob- tained, three produced very beautiful green-bodied hymenoptera, and an Apanteles sp. emerged from one of the Catocala larva after it had spun its cocoon. Arti- ficial control experiments were not very satisfactory owing to the difficulty in maintaining controls. An ordinary hand sprayer was used and mixtures con- taining Paris green sprayed into the cracks where colonies existed, but without any effect whatever. Pieces of sodium cyanide placed in the cracks destroyed the colonies completely in twenty-four hours. The best control, however, was the simple one of carefully pruning away the splitting bark from around pruning wounds and other places in the tree where the bark naturally breaks away. The adult of the larvae is evidently an opportunist, laying its eggs in these cracks as it finds them. Cleaning up such places improves the appearance of the tree, involves the destruction of all the season’s hatch, and reduces future breeding places. As cottonwoods are usually grown in small numbers as shade trees and windbreaks, such a plan is practical. The tree survives the presence of the colonies, but the larvae spoil its appearance, with masses of faecal matter, and keep wounds open, causing decay. Several trees were noticed in which such places were full of water, and har- bored numberless dipterous larvae which fed on the decaying matter. PTA . . a Rls . . . "he tree, once it attains a fair size is apparently immune, as none of the mature trees in the river bottom at Lethbridge showed any sign of the presence of larvae. The habits of Ufeus in thus using cottonwoods as a breeding ground is apparently of wide occurrence, since in Montana Ufeus on cottonwoods is re- ported in several of the yearly reports of that state. THE CANADIAN ENTOMOLOGIST. 27 SOME NEW AND RARE COLEOPTERA FROM SOUTHWESTERN FLORIDA BY W. S. BLATCHLEY, Indianapealis, Ind. (Continued from Page 14) Eros trilineatus Melsh.—An individual of this species was taken at Dunedin having the left elytron only two-thirds the length of the right one. Chauliognathus marginatus Fab. Examples of this common species are at hand from Miami and Everglade having the thorax entirely yellow and the black spots on head very small. Belotus (Lobeius) abdominalis (ec.)—Taken at Dunedin in some numbers, April 10—15, by sweeping the new low vegetation on lots which had been re- cently burned over. Schwarz records it as “common on swampy meadows in June.” Attalus australis sp. nov. Oblong-oval, wider behind. | Black, strongly shining, elytra faintly tinged with blue; femora shining black; labrum, palpi, antennae, tibiae and tarsi, pale reddish-yellow ; upper surface thinly clothed with sub-erect grayish pubescence. Head wider than long, narrower than thorax, almost impunctate; eyes large, prominent; antennae reaching middle of body, male, base of thorax, female ; rather stout, not serrate, the joints one-half longer than wide. Thorax sub- orbicular, two-thirds wider than long, front margin truncate, disc very minutely and sparsely punctate. Elytra not wider at base than thorax, gradually ex- panding and widest about apical third, finely but more distinctly punctate than thorax, each puncture, as there, bearing a sub-erect grayish hair. Length -1.3-1.8 mm. Swept in some numbers, Feb. 21-27, 1919, from low vegetation along the inner margin of the beach at Cape Sable. The pale tibiae and tarsi contrast strongly with the black femora. ‘The blue-black upper surface and posteriorly widened elytra give it the appearance of a Pseudobaeus, but the male and female elytra are similar in form. Melyrodes (Melyris) basalis (Lec.)—One specimen taken at Dunedin, Apri! I1, by sweeping ferns in Skinner’s Hammock. ‘The only other definite Florida record is that of Dozier! who has taken it at Gainesville. Cymatodera undulata (Say)—One specimen at Dunedin, February 23, by beating bunches of Spanish moss. No previous Florida record except that of Leng in his Catalogue. Thanasimus dubius (Fab.)—One, February 17, beneath a stick of corded pine wood near Dunedin. ‘The first record for the State, though the general range is given by Leng as Canada and New England to Mexico. Hydnocera humeralis Say.—One, April 12, at Dunedin by sweeping low vegetation in dry, sandy soil. No previous definite station record for the State. 14Ent. News, XXIX, 332, 28 THE CANADIAN ENTOMOLOGIST. Zonitis schefferi sp. nov. Elongate, subcylindrical. | Head yellow, with a large subquadrate piceous spot between the eyes; antennae piceous, the basal joints black; thorax yellow with a rosaceous tinge; elytra piceous, with narrow sutural, median and marginal stripes yellow; under surface and legs black, shining, the trochanters wholly, and coxae in part, yellowish. Head subquadrate, coarsely and densely punctate ; eyes transverse, widely separated above and beneath; antennae stout, slightly less than half the length of body. ‘Thorax slightly wider than long, sides almost straight from base to apical third, hind angles rounded, disc densely and coarsely punctate, a median impressed line on basal half. Elytra densely and coarsely rugose-punctate. | Under surface rather finely, not densely punctate ; last ventral with a very broad U-shaped emargination. _ Length 9 mm. Described from a single male beaten, February 9, from dead vines by the side of a roadway running through Skinner’s hammock near Dunedin. In form and sculpture it resembles Z. longicornis Horn, but the antennae are stouter and much shorter and they and the legs are almost wholly blackish. The median discal stripe of elytra narrows gradually from the base and does not reach the apex. Named in honor of Chas. Scheffer of Brooklyn, New York, who, by his careful and discriminating studies has done much to advance our knowledge of the Coleoptera of North America. Phomalus (Xylophilus) brunnipennis (Lec.)—A single specimen was beaten from a bunch of Spanish moss near Dunedin, on March 23. ‘This is the first Florida record, though it is said to range from the District of Columbia and Indiana to Southern California. It is placed in the family EKuglenidae by Leng. Drapetes geminatus Say.— Drapetes quadripustulatus Bony.—While these two species have been men- tioned as occurring in Florida by a number of persons, definite recorded stations from the State are very few. One specimen of each has been taken at Dunedin, geminatus on April 14 by sweeping ferns in a dense wet hammock, and quadripustulatus on April 12 froma low huckleberry on dry sandy soil. Schwarz records both as “very rare,” geminatus from Enterprise and quadripustulatus from Tampa. Buprestis striata impedita Say—One example of this handsome Buprestid was taken March 7, from a window of my residence in Dunedin. Not before known from Florida, and perhaps an adventive. Cyphon americanus Pie—This is the C. impressus Lec. described!® in 1878 from specimens taken by Schwarz on swampy meadows at ‘Tampa and Enterprise, and not since recorded from the State. It occurs in small numbers about Dunedin in April, in company with C. variabilis Horn, on the flowers and foliage of huckleberry. LeConte’s name was preoccupied. Scheffer (Ms.) states that, “as far as known, the elytral impressions are present only in the females.” Trogoderma flabellata sp. nov. Oblong-oval. Black, shining, rather densely clothed with fine pubescence which is blackish and suberect on head and thorax, yellowish and subprostrate 15Proc, Amer. Phil. Soc., XVII, 405, ee ee oe ae ee ee meen Te eee Tar, oT SO ee re, 1G Sa 4 PR! Ue Nae SO is Loar h: See eri THE CANADIAN ENTOMOLOGIST. 29 on elytra; each elytron with a narrow irregular orange-red band just in front of middle, this concave behind and widest near the suture; femora and antennae fuscous ; tibiae and tarsi reddish-brown. | Head densely and finely punctate ; eyes entire, separated by three times their own diameter. Antennae flabellate, the branches of joints 4 to 10 three or four times the length of the segments, those of two and three shorter. Thorax about twice as wide as long, sides broadly rounded, base as wide as elytra, strongly bisinuate, disk densely and finely punctate. lytra conjointly scarcely twice as long as wide, finely and rather closely aciculate punctate. | Prosternum very coarsely and closely punctate, the process feebly carinate. Length 2.1-2.3 mm. Described from two males, one taken at Dunedin, February 14, the other at Caxambus, March 9; both by sweeping low shrubs along tidewater lagoons. In general appearance this is a miniature of my 7, fascifera, but the flabelate antennae, narrower cross band of elytra, more coarsely punctate prosternum and much deeper antennal fossae are, in addition to its small size, distinctive characters. Trogoderma fascifera Blatch.—A second male of this species was beaten, March 22, from dead leaves of a cabbage palmetto on Hog Island. The unique type was from the shore of Lake Istokpoga. Tenebroides obtusus (Horn.)—One specimen, January 21, from beneath bark of a pine block at Dunedin. Described!® from Pennsylvania and District of Columbia, and not heretofore known from Florida. Lophocateres pusillus (IKtug.)—One specimen, February 6, from beneath a board tying on the ground in a barnyard near Dunedin. An introduced species originally described from Siam, and known in this country from South Carolina, Louisiana and Texas. Cybocephalus nigritulus Lec—Examples of this minute Nitidulid have been . taken on Hog Island opposite Dunedin, in February and March, by beating the Florida button-bush, Conocarpa. erecta L. ~ Lathropus vernalis Lec—One specimen swept, March 29, from huckleberry blossoms near Dunedin. Hitherto known from the State only from Crescent City. Aulonium tuberculatum Lec—Several specimens were taken near Dunedin in January, in company with Lasconotus pusillus Lec., and Hypophloeus thoracicus Melsh., beneath the bark of freshly cut pine blocks. It is noted in the Schwarz Manuscript as found at Jacksonville by Ashmead. Monocdus guttatus Lec—A number of examples were taken at Chokoloskee by beating its host plant, the slender twining milkweed, Metastelma scoparium ~ Nutt. In normal specimens the body is covered with a whitish waxy secretion. In some of those from Chokoloskee this was lacking and the usual small scattered dark spots of elytra were very faint or wholly wanting. Alphitobius piceus (Oliv.)—Nearly a hundred specimens of this cosmopolitan species were taken March g in company with scores of Dryotribus mimeticus Horn from beneath two pieces of decaying lumber near an old sugar furnace at Caxambus. Single specimens have also been found on two occasions at Dunedin. 16Proc, Acad. Nat. Sci. Phil., 1862, 87. 30 THE CANADIAN ENTOMOLOGIST. Ptinus constrictus sp. nov. Elongate, subparallel. | Dark reddish-brown, the antennae, legs and under surface slightly paler. Head coarsely and densely punctate, clothed with sub- erect yellowish bristle-like hairs; occiput with a deep median groove; eyes quite prominent, coarsely facetted; antennae three-fifths the length of body, joints 2 and 3 each two-thirds the length of 4, 4 to 11 subequal, densely pilose. Thorax subcylindrical, strongly constricted near base, both disc and constriction densely and coarsely punctate, the former bearing each side near the middle a triangular tuft of stiff yellowish hairs. Ejlytra three times as long as broad, sides parallel ; striae feebly impressed, marked with rows of fine, close-set punctures; intervals about twice the width of the striae, each with a row of minute punctures, the punctures of both striae and intervals each bearing an inclined yellowish hair. Sterna smooth, glabrous; abdomen thickly clothed with fine yellowish pubescence. Length 2.6 mm. A single male was beaten, March 15, from dead branches in a partially cleared mangrove swamp on Chokoloskee Island. Mr. Fall, to whom it was submitted, stated that in his table!’ it should probably be placed between strangulatus and fall. Onthophagus alutaceus Blatch.—This species was described!* from a unique. taken on the wing at Dunedin. A second specimen was obtained January 21, by beating the foliage of a water oak near the bay front, one mile north of the town. ‘The representatives of the genus usually occur on the ground about carrion, horse dung and other refuse. Ligyrus subtropicus sp. nov. Oblong, suboval, very robust, convex. | Above piceous-black or very dark chocolate-brown, strongly shining; under surface and appendages dark reddish- brown. Head at widest part two-fifths the greatest width of thorax, finely and shallowly rugulose; clypeus subtriangular, its sides rapidly converging from the very broad base, its apex bifid, the teeth upturned and well separated, extreme base with two blunt tubercles behind which the interocular space is visibly con- cave. Thorax one-third wider than long, sides broadly curved, hind angles rounded, dise finely, sparsely, irregularly aciculate-punctate and very minutely alutaceous; front margin with a short blunt median tubercle behind which is a shallow oval pit or impression, this punctate like the disc. Elytra as wide at base and just twice as long as thorax, their tips broadly rounded and exposing both the last dorsal segment and the very large pygidium; dise with sutural striae well marked, the others feeble and irregular, all with coarse punctures extending throughout the length; first, third and fifth intervals much wider than the others, and with numerous confused punctures as coarse as those of the striae. Pygidium minutely scabrous at base, elsewhere very finely and sparsely punctate. Ventral abdominal segments very finely and remotely punctate, each with a single interrupted transverse row of much coarser punctures. Middle of prosternum and median tubercle behind the front coxae each with a tuft of 17Trans, Amer. Ent. Soc., XXXI, 1905, 113. 18Can. Ent., LI, 1919, 31. z THE CANADIAN ENTOMOLOGIST. 31 long reddish bristles. Front tibiae with three large anterior teeth and a very small posterior one. Length 27 mm., width 13 mm. A single female of this large Scarab was taken at light at Dunedin, June 4, 1913, and has since been in my collection without a name. _ I finally sent it to Mr. Fall, who returned it as a “Ligyrus near to bryanti Rivers, which it is not.” Col. Casey then passed judgment upon it as follows: “Your specimen _ belongs to my subgenus Grylius and represents a species near to the Florida _ individual described by me?® as laevicollis Bates, but is a different species. It is larger and much stoiter, has coarser elytral punctures and a different form of pronotal apical impression.” Euphoria sepulcl.rclis floridana Casey —The types of this sub-species?° were from the “East Coast of Florida, Jacksonville to Palm Beach.” A specimen at hand was taken at Ocala on April 14. Euryptera lateralis (Oliv.)—A dozen examples of this handsome Lepturid were taken February 21 from the blossoms of a Cherokee rose, in my lot at Dunedin. It is listed by Schwarz as “very rare’ at Tampa and Enterprise, and has been taken also at St. Augustine and Crescent City. Euryptera flavatra Blatch—A second example of this bicolored species was taken from a blossom of the same rose on April 9. Only the unique type, _ described?! from Dunedin, was previously known. Leiopus maculipennis sp. nov. Oblong, moderately robust. Above dull reddish-brown, thickly and evenly clothed with short. prostrate grayish-yellow hairs, with small patches of white and black ones intermixed; the white patches alternating with the black along each sutural carina, forming a narrow, much interrupted bar across elytra at apical third, and sometimes another half way between it and apex, the black -patches arranged in four rows as suberect tufts along the disc of each elytron; antennae and legs indistinctly but perceptibly annulate, the apical third of middle and hind tibiae fuscous; under surface piceous, thickly clothed with long grayish irs. Antennae surpassing tips of elytra 3-5 mm., the basal joint thick, sub- clavate; second one-fourth longer than any which follow, these being subequal. Thorax more than one-third wider than long, sides almost straight from apex to summit of lateral tubercle, which is short, subacute and placed at basal fourth; disk very finely and densely punctate. Elytra one-third wider at base than thorax, sides straight to apical third, tips subtruncate, the sutural angle slightly prolonged ; disk finely and rather sparsely punctate. First joint of hind tarsi as long as the next two. Length 5.5-6.5 mm. <- as Described from ten specimens taken at Dunedin; one December 5, the _ others between March 12 and April 19. Occurs on dead vines and twigs in dense hammocks. This species has been in my collection unnamed since 1916, and specimens have been compared with those of all other species in the Horn and LeConte collections at Philadelphia and Cambridge, and also by Mutchler Memoirs VI, 1915, 190. 20Memoirs VI, 1915, 321. 21Can. Ent. XLVI, 1914, 92. 32 THE CANADIAN ENTOMOLOGIST. with those in the American Museum. It belongs in the group with crassulus and centralis Lec., but differs from all our described species in lacking all trace of dark bands on the apical half of elytra, in the very distinct and handsome maculation of the sutural carinae, etc. Oberea flavocephala sp. nov. Elongate, subcylindrical. | Black, strongly shining, thinly clothed with minute grayish pubescence and scattered erect black hairs. Head and thorax bright yellow, the former with two spots on occiput, one behind each eye and labrum and mandibles black; thorax with two large callosities, a small sub- quadrate spot in front of scutellum and a triangular one each side on lower posterior flank, shining black; tibiae and tarsi piceous. Head coarsely and densely punctate; antennae a little shorter than body, the outer joints slightly stouter than the third and fourth. Thorax coarsely and closely punctate, the two black callosities twice or more as large as in dimaculata, each circumscribed near the edge by a series of very coarse punctures. Elytra with rows of coarse, dense punctures, the intervals very narrow, the third slightly raised nearly throughout its length; tips truncate, their inner and outer angles distinctly pro- duced or dentiform. | Abdomen finely and very sparsely punctate. Length 8.5-9.5 mm. Two swept from low herbage along the margin of a dense hammock near Dunedin, April 9-24; one from Ormond, April 14. | The Ormond specimen, taken in 1913, was labelled bimaculata Oliv., but on taking the two Dunedin examples I saw that they differed widely from that species in the yellow head, large coarsely punctate thoracic callosities and armed elytral tips. __ It is evidently allied to insignis Casey22 from North Carolina, but that is a larger species with rounded spot in front of scutellum and elytral tips unarmed. Cryptocephalus calidus Suffr—This species occurs in dry localities about Dunedin during December and January, on the foliage of huckleberry and other low shrubs. _ I first recorded it from there in 1917, but Leng does not definitely include Florida in its distribution. Cryptocephalus aulicus Hald—Three specimens were swept on April 8, from low vegetation along the edge of a hammock. Disonycha caroliniana (Fab.)—In the Schwarz Manuscript this species is mentioned as occurring at Enterprise and Ft. Capron. A single specimen was taken December 16 by sweeping near Dunedin. Colaspidea insularis sp. nov. Oblong-oval, convex. srown with a shining brassy tinge, antennae, tibiae and tarsi paler; surface sparsely but evenly clothed with white scale-like hairs. Head with front finely and sparsely punctate, and with a broad, shallow median impression; antennae slender, reaching middle of elytra, joint two equal in length but more slender than one, curved, 3-6 subequal to two, 7-10 stouter, subequal in length. Thorax one-half wider than long, its front margin curved and somewhat projecting to cover occiput; sidés broadly rounded, disk finely “2Memoirs IV, 370. » as THE CANADIAN ENTOMOLOGIST. 33 not closely punctate. Elytra conjointly oval, one-fourth wider at base than thorax, umbone prominent; disk evenly, closely and rather finely punctate, the umbone and three or four elongate calloused spaces near middle of each elytron smooth. Under surface very finely and sparsely punctate; prosternum forming a large flat quadrate plate between the front coxae. Length 2.7-3 mm. Described from three specimens from the Isle of Pines received, among other material for naming, from Prof. J. R. Watson, of the Florida Agricultural Experiment Station. They were labelled ‘“‘on citrus,” and Prof. Watson writes that he has considerable correspondence with citrus growers on the Isle of Pines, who are unable to get satisfaction from the Cuban,station. Four species of Colaspidea have hitherto been described from North America, all from Southern California or adjacent islands. According to Horn,?* others are known “from Southern Europe and the circum-Mediterranean region generally.” Since Leng and Mutchler mention no species of the genus in their list of West India Coleoptera, insularis is apparently the first one to be known from the Atlantic region of North America. Haltica schwarzi Blatch.—Described?* from the east shore of Lake Okeecho- bee. [wo specimens were secured on March 4 while sweeping low huckleberry near the edge of a brackish water marsh just east of Ft. Myers. TWO FAMILIES OF INSECTS NEW TO BRITISH TERTIARY STRATA BY T. D. A. COCKERELLs University of Colorado. When recently examining some hitherto overlooked fossil insects in the British Museum, I found two specimens collected by Mr. a’Court Smith in the Isle of Wight, representing families not yet recorded from the British Tertiary rocks. They come from the Bembridge series, at the famous Gurnet Bay locality. La a eee Fig. 1, wing of Vectevania vetula; Fig. 2, wing of Nemoura priscula. EVANIIDAE. Vectevania n. gen. Cu Related to Protofoenus Ckll., from Burmese amber, but differing especially in the complete third discoidal cell and the deep triangular stigma. The second transverse-cubital nervure is so faint as to be practically obsolete, and there is perhaps a slight indication of the third, too vague to be positively recognized. 23Trans. Amer. Ent. Soc., XIX, 1892, 204, 24Can. Ent., XLVI, 1914, 141. 34 THE CANADIAN ENTOMOLOGIST. The position of the second is as in the living Neuraulacinus braunsi Wieffer. The small cuneiform first discoidal cell is characteristic, and the comparatively distinct venation of the hind wings is a primitive feature, lost in the modern Aulacinus, but preserved in Neuraulacinus. Vectevania vetula n. sp. claviform, nearly 3 mm. long, obtuse at apex; anterior wing about 4.5 mm. long, clear hyaline, with ferruginous nervures; stigma margined with brown, apparently originally all brown. British Museum, In. 20535. Head narrower than thorax; thorax elongate-oval, 2 mm. long; abdomen PERLIDAE. Nemoura (sens. lat.) priscula n. sp Anterior wing, length about 5.4 mm., width nearly 2 mm_; colorless. About 1.7 mm. of the base is lost. The venation is very simple, but similar in principle to that of Nemoura. From the fork of the radial sector to the apex is nearly 3 mm. Comparing the venation with recent species, I found nothing very close, and it is probable that a distinct genus is indicated. Some of the species from Prussian amber are interesting for comparison. Thus Taentopteryx elongata Berendt has the cross-nervure at the end of the subcosta, but it is oblique. Leuctra gracilis Berendt and Leuctra linearis Berendt have this cross-nervure well before the end of the subcosta, in gracilis producing an angulation of the subcosta, but not in linearis. On the other hand, L. gracilis agrees with the English fossil in having the cross-vein connecting R with R, beyond the fork of R,; in the other two amber species it is at the fork. Our fossil nearly agrees with L. gracilis in the position of the cross-vein between R, and M. British Museum, In. 17408. Thirteen species of Perlide have been found in Baltic amber, and one in the Oligocene of Rott, but strangely enough none in the American Tertiaries. UNDESCRIBED LEPIDOPTERA IN THE CANADIAN NATIONAL COLLECTION. BY J. MCDUNNOUGH; Entomological Branch, Ottawa.* For some time there has been a strong feeling among Canadian entomologists that the types of as many as possible of our Canadian insects should be deposited in the National Collection at Ottawa. During the past half century, owing to the lack of taxonomists in Canada, a large proportion of Canadian insect material has been sent to the United States or Europe for identification and as a result the types of numerous undescribed species have been retained in these countries. | With the growth of taxonomy and the dis- covery of numerous closely allied forms which heretofore had been grouped *Contribution from the Entomological Branch, Department of Agr., Ottawa 7 y ‘ i ; -*~ / ere’ o> Be ber bees gE Dew ~ aati ype WARE re > THE CANADIAN ENTOMOLOGIS'T. 35 Can. Env. Vot. LIv. PLATE 1. UNDESCRIBED LEPIDOPTERA. Male clasper of 1. Exrartema permundanum Clem.; 2. E. troglodanum n. sp.; 3. E. furfuranum n. sp.; 4. HE. rusticanum n. sp.; 5. E. bolanderanum n. sp.; 6. E. terminanum n. sp.; 7. Argyroploce youngana n. sp.; 8. A. deceptana n. SDp.; 9. A. tertiana n. sp.; 10. A. buckellana n. sp.; 1. A. polluzana n. sp.; 12. A. castorana n. sp.; 13. A. aspasiana n. sp.; 14. A. carolana n. sp.; 15. A. vulgana n. sp. 30 THE CANADIAN ENTOMOLOGIST. under a single specific name, the necessity for a study of type material becomes — greater and greater; the disadvantages under which a Canadian entomologist _ labors, where such study involves numerous expensive journeys, become yearly more obvious, and it is with the sole end in view of adding to the type material in the National Collection that the following paper has been prepared. It is possible that in a few instances a named species has been redescribed, as certain identifications. have been based on descriptions alone and a study of type material has been impracticable; if such cases should occur, the error may be ascribed to my anxiety to secure as many types as possible for the Ottawa Collection. SCOPARIINAE. Scoparia truncatalis sp. n. Allied to basalis Wlk. but with broader and shorter wings and with no olivaceous scaling around the reniform; the genitalia are also distinct. Primaries gray, shaded with smoky; a very short black basal dash; a dark t. a. line, rounded outwards below costa and starting from a small dark costal spot, shaded slightly inwardly with white; included basal space smoky; orbicular occasion- ally represented by a dark dot close to t. a. line; claviform a dark streak attached to t. a. line; reniform formed by two blackish cusps, making an x-shaped mark; above this some smoky shading but remainder of median space rather pale gray; t. p. line rounded outwardly below costa, then inwardly oblique and minutely dentate. white, shaded on both sides with smoky; terminal space whitish with smoky blotch at centre of outer margin and prominent terminal row of dark spots just inside margin of wing, which appears as a white line. Fringes pale smoky cut by a darker line. Secondaries whitish, slightly smoky outwardly. Expanse 15 mm. Holotype,—1 8, Norway Point, Lake of Bays, Ont. (July 12) (J. Mc- Dunnough), in Canadian National Collection. Paratypes—6 6’s, 1 9, same locality and date; 1 3, 3 9’s, Ottawa, Ont... “(july5, 9, 11) (Ce Younes, As compared with basalis the male claspers are much broader and the aedoeagus contains a bundle of two or three long spines. PHYCITINAE. Acrobasis alnella sp. n. Primaries dark purplish gray with slight ruddy reflections and paler gray shading; t. a. line arising from a triangular dark shade on costa, well outcurved to cell, then straight to inner margin, pale gray, bordered by a dark line; the space between it and the dark basal scale-ridge dull clay color, median space with paler gray shading below costa and two superimposed black discal dots; t. p. line straight below costa, bulging gently opposite cell and finely dentate, whitish, bordered inwardly by a dark line. A dark terminal line. Secondaries dull smoky. © On the underside the male is without black markings. | Expanse 17-22 mm. . aS ree ‘* _ a - - a a oe ee THE CANADIAN ENTOMOLOGIST. a7, Holotype,—1 ¢, Ottawa, Ont. (July 9) (J. McDunnough), bred from Alder, in Canadian National Collection. Paratypes,—4 é’s, 3 2’s from the Ottawa region, bred from Alder on various dates in July. The species is closely allied to betulella but smaller and shows genitalic differences, notably in the much smaller gnathos; the cocoon is oval, much like a miniature betulella cocoon. From rubrifasciella, also an Alnus feeder, it is at once distinguished by the lack of the bright red antemedian band. It may possibly be normella Dyar, the food plant of which was not given in the des- cription and the type of which I have not studied. * EUCOSMIDAE. Exartema Clem. In working over the material in the Canadian National Collection be- longing to this genus (i.e. species with a cylindrical appendage at base of secondaries’'in the male sex) an examination of the genitalia soon made it apparent that on the one hand there was a group of species very similar in general superficial appearance but differing markedly from each other in genitalia, whilst on the other hand species which could be readily distinguished from each other by maculation and color possessed genitalia so similar that no definite points of distinction could be found in these organs. The first group centers around permundanum Clem.; our determination of this species is based on a study of the descriptions of Clemens and Zeller and agrees with specimens in the collection determined as this species by Kearfott and Busck; a figure of the clasper is given (c. f. fig. 1). As at the present time it is impossible to examine Walker’s type specimens the synonymy as given in Dyar’s List is accepted. Several apparently unnamed species are herewith described. Exartema troglodanum sp. n. (Fig. 2). Maculation very similar to that of permundanum but the general im- pression given is that of a much darker insect due to the dark bands being thickly covered with rather bright brown scales; the pale lines defining these dark areas are also much less evident in this new species than in permundanum. Basal dark area slightly sprinkled with light scales, its outer border is outwardly oblique from costa at 1% to center of wing, then almost perpendicular to inner margin with a slight concavity in the fold. The median band shows very dark shading at costa and the same: two projections of the outer border found in permundanum, below these the band is completely cut by a narrow line of paler ground color. The anal spot is large and triangular and the oblique subapical dark band is broadly joined to the first dark costal spot. Pale areas with considerable purplish silvery iridescence and cut by a central dark line; fringes pale yellowish, cut at apex and above anal angle with dark scales. | Secondaries dark smoky with pale fringes. Expanse 16-18 mm. Holotype—1 ¢, Meach Lake, Que. (C. H. Young) (June 17), in Canadian National Collection. 38 THE CANADIAN ENTOMOLOGIST. Paratypes,—1I 8,2 9’s, Ottawa, Ont. (C. H. Young) (June 27, 28), 1m same Collection. Exartema furfuranum sp. n. (Fig. 3). Color and maculation of permundanum but slightly more greenish olivaceous and with the pale areas much more strigate with darker lines and dashes; all dark bands very distinctly outlined with pale ochreous. ‘The two outer projections of the median band are very long, the upper one almost touching the oblique subapical band which ends at a point opposite this tooth and does not connect with the dark costal spots. Fringes dusky. Secondaries deep smoky with paler fringes. Hxpanse 16 mm. Holotype,—1 8, Ottawa, Ont. (C. H. Young) (June 20), in Canadian National Collection. Paratypes——1 8,1 9, Meach Lake, Que. (C. H. Young) (June 20, 21), in same Collection. Exartema rusticanum sp. n. (Fig. 4). Usual type of maculation; pale areas very decidedly silvery-purplish; dark bands suffused with ruddy scales, especially prominent in outer areas (in worn specimens not so noticeable). The two outer projections of median band are short and the lower one quite thick, the space between the two contain- ing a pale ochreous spot; there 1s also a bluish spot at base of lower tooth enclosed in dark area; the triangular anal spot is generally connected with the oblique subapical band by a fine network of lines, as is also this band with the first costal spot. A thick dark line at base of fringes which are pale, checkered irregularly with black. Secondaries dark smoky. Expanse 15-16 mm. Holotype-——1 8, Onah, Man. (N. Criddle) (July 17), in Canadian National Collection. Paratypes,—2 $’s, 2 9’s, Onah, Man. (N. Criddle) (July 17-19), in same Collection. The genitalia are similar to those of the preceding species but the two species can be readily separated by color and maculation. A @ specimen from Trenton, Ont., appears to belong here; it had been identified by Kearfott as zellerianum Fern. but Zeller’s figure represents quite a different type of macula- tion and I cannot agree with this determination. Exartema fraternanum sp. n. Very similar to preceding species in maculation and genitalia but lacking the ruddy tinges and with pale areas distinctly less silvery, resembling in this respect a small dark form of permundanum. The teeth of the median band are less blunt and wider apart than in rusticanum and there is no pale area below the inner tooth with the exception of a couple of hair-lines joining the costal and inner portions, this latter being goblet-shaped with short stem resting on. inner margin. Oblique subapical band dark, much thickened in upper portion, joined by a fine line to costal spot and also to anal triangular spot. Secondaries dark smoky with pale fringes. Holotype—t1 @, Ottawa, Ont. (July 3) (C. H. Young), in Canadian National Collection. = Jn « % ¥ * a a THE CANADIAN ENTOMOLOGIST. 39 Exartema bolandanum sj. n. (Mig. 5). Very similar to olivaceanum Fern. and of the same type of genitalia; the general appearance of primaries is more mottled than in olivaceanum; the best point of distinction is found in the subterminal area, the oblique band being broader and closer to apex of wing in bolandanum with a narrow line of dark scales extending down to anal angle; the apex of the triangular dark spot on inner margin is joined to the center of the oblique band by a narrow dark line and the included pale space above tornus is bisected by another dark line running from the first line to anal angle. Fringes pale at apex and anal angle, dark centrally. Expanse 13 mm. Holotype—t1 4, Ottawa, Ont. (June 10) (C. H. Young). Exartema versicoloranum (lem. Exartema versicoloranum Clem. 1860, Proc. Acad. Nat. Sci. Phil., 357. Sericoris versicoloranum Clem. 1865, Proc. Ent. Soc. Phil., 136. The original description of this species is very vague and might apply to several species; in his second paper however Clemens states that the species is ordinarily distinguished by the white or yellowish-white costa at the base of wing and the white space toward the hinder margin. There is a single 4 specimen in the Canadian National Collection from Trenton, Ont. (Aug. 1) which agrees with the above diagnosis, but differs markedly in genitalia from an Ottawa series, captured in June, under the same specific name. As however this latter series fits in excellently with Zeller’s description of appendiceum, at present listed as a synonym of versicoloranum Clem., I propose to use versicoloranum Clem. for the species with white costa at base and resurrect appendiceum Zell. from the synonymy for the very similar species with dark basal area. Exartema valdanum sp. n. Basal and median areas dark olivaceous black-brown, separated by a band of whitish color containing a few dark dots in form of a broken central line; this pale band is upright with margins slightly waved. Median band outwardly with two blunt teeth and an indentation of pale color below inner tooth. The usual dark triangular spot near anal angle and an oblique band running inward from center of outer margin and joined to first costal spot by fine line; a narrow dark area below apex sending hair-lines to costal spots and separated from subapical band by a narrow band of whitish. Remainder of outer area pale, same color as inner band, slightly clouded with smoky. Fringes irregularly checkered black and white. “ Secondaries dark smoky with pale fringes. Expanse 17 mm. Holotype—1 2, Ft. Coulonge. Que, (July 7) (S. A. Graham), in Canadian National Collection. Allotype,—1 ?. Aylmer, Que. (May 29) (J. McDunnough). The type of genitalia is that of permundanum but the pale bands of primaries rather recall fasciatanum Clem. Exartema nananum sp. n. Thorax light brown; primaries with usual type of maculation, the dark 40 THE CANADIAN ENTOMOLOGIST. areas cinnamon-brown, the pale bands and spots bluish-silvery. Basal area with outer margin bulging outwardly, sprinkled with a few bluish scales in costal — half of wing. Antimedian pale band cut by a central brown line. Median brown band with inner margin slightly concave, composed of an upper boot-— shaped spot and a lower subquadrate spot joined together narrowly at heel of boot and also near the toe, enclosing a pale bluish spot; there is also a projection © on outer margin of the band below costa. The subapical oblique band is — thickened in its middle and joined to the first costal spot, the toe of the boot and the anal triangular spot by fine lines, the enclosed areas being of the bluish- — silvery color of the antemedian band. Terminal area narrowly brown with a fine bluish line bordering the oblique band outwardly. A dark terminal line. Fringes slightly bluish with dusky apical and median areas. | Secondaries smoky with lighter fringes. Expanse 12 mm. Holotype—t1 8, Mer Bleue, Ottawa, Ont. (July 20) (C. H. Young), in Canadian National Collection. The type of genitalia is that of permundanum. Exartema bicoloranum sp. n. Primaries cinnamon-brown beneath which towards the base an underlying area of black scaling may be seen with a lens; all maculation very indistinct, consisting of the usual bands and spots in a slightly deeper brown than the general ground color, rather better defined in outer area, where the outer edge of the median band, the anal triangular spot and the oblique subapical band are visible, the latter defined by narrow lines of purplish; a dark terminal line; fringes pale ochreous tinged with smoky. Secondaries pure white, with a smoky terminal border, broadest at costa; fringes pale. Expanse 13 mm. Holotype-—t é, Barrington Passage, N.S. (July 10) (C. H. Young), - in Canadian National Collection. The type of genitalia is similar to that of furfuranum and rusticanum; the white secondaries readily distinguish the species from others of the genus. Exartema submissanum sp. n. Primaries dull cinnamon-brown with a purplish tinge due to a strong >triation of brown scales on a purple ground color; maculation very indistinct, best defined in terminal area, brighter brown than ground-color without purple tinge. Median band with a sharp outward angle below costa, then more or less perpendicular to inner margin, rather narrow; anal triangular spot small, more or less joined to median band; oblique subapical band most distinct of all the maculation, narrow, of even width throughout, joined by a fine line to first costal spot; apex streaked with brown. Dark terminal line; fringes pale ochreous, shaded with smoky. Secondaries whitish hyaline at base shaded with smoky outwardly, forming a more or less diffuse outer dark border. Ex- panse 16 mm. | Holotype—1 @, Ottawa, Ont. (July 23) (C. H. Young), in Canadian National Collection. - Paratypes—3 6’s, 1 9, Ottawa, Ont. (July 17, 23) (C. H. Young), in same collection. THE CANADIAN ENTOMOLOGIST. 4! The species resembles somewhat the preceding but is larger with less distinctly white secondaries and the genitalia are of the permundanum type. According to Zeller’s figure and description it would appear to be fairly close to gelleranum Fern. lacking however the prominent tooth of the median band. Exartema terminanum sj. n. (Fig. 6). Basal 4/5 of primaries deep purplish-black with a few purple shining striae arising from pale costal spots antemedially indicating the usual pale band. The outer 1/5 of wing is pale ochreous crossed by the blackish subapical band which loses itself in the dark area, is of even width throughout and slightly bent; a few dark streaks at apex and tornus of wing. The usual dark median band is slightly indicated by curved purple striae on its outer edge. Fringes pale ochreous tinged with smoky. | Secondaries light smoky. paler in basal area. Expanse 14 mm. Holotype—1 ¢, Ottawa, Ont. (July 1), (J. Fletcher), in Canadian National Collection. Paratypes,—1 6,2 2’s, Ottawa, Ont. (July 10, 14, 28) (C. H. Young), in same collection. This may be merely a form of concinnanum Clem. as it has the same type of genitalia. In any case, on account of the striking coloration, it would seem worthy of a name. Argyroploce capreana Hbn. There are before me four species belonging to this group and all closely allied. Capreana may be best distinguished by a small comma-like white mark jutting in from the white apical area to the outer margin of the dark basal area about the center of the wing. It is represented in the National Collection by specimens from Ottawa, Trenton and Sudbury in Ontario, one male from -Nordegg, Alta., and one male from Vancouver, B.C. If identifications made by Mr. Kearfott are correct, frigidana Pack. would appear to be a synonym of this species. The other species appear to be undescribed. I have carefully compared them with existing descriptions of North America species and also figures and descriptions of the allied European species and cannot match them. I therefore offer the following descriptions. Argyroploce youngana sp. n. (Fig. 7). Rather larger than capreana but very similar in general appearance. Basal 2/3 of primaries dark purplish-brown, blotched with still darker markings; the costal area, however, for about half the length of wing, is shaded with white, enclosing a quadrate dark patch near base of wing. The outer margin of the dark area is sharply and evenly defined, being perpendicular to below cell, then forming a distinct angle and outwardly oblique to inner margin just before tornus. Apical 1/3 white, clouded with purple-gray at apex, with two dots of similar color on costa from which proceed faint wavy subparallel gray shades crossing obliquely to outer margin. Fringes smoky slightly checkered. Second- aries dull smoky with paler fringes. Expanse 19-20 mm. 42 THE CANADIAN ENTOMOLOGIST. Holotype,—1 &, Meach Lake, Que. (July 20) (C. H. Young), in Cana- dian National Coilection. Paratypes,—t 6, Chelsea, Que. (July 6); 6 9’s, Meach Lake (Aug. 5), Ottawa, Ont. (July 4, 6, 11, 25, 28) (C. H. Young). The male genitalia have the arm of the clasper narrowed for a consider- ably greater length than is found in capreana; there are also differences in tue gnathos and the spining of the aedoeagus. Argyroploce deceptana sp. n. (Fig. 8). Much smaller than preceding species; evidently allied to the European sauciana. Basal 2/3 of primaries brown, slightly sprinkled with white scales forming a more or less evident dash from base through center of wing; a small dark quadrate patch on costa near base and a larger one near outer edge of dark area; several irregular dark blotches in central portion of wing. Outer 1/3 of wing white, the dividing line not very sharply demarcated; a white hook projects into the dark area below cell, leaving a distinct blackish ocellus-like mark, much as in separatana Kft., standing out on the margin of the white area; a triangular anal spot is partially separated by pale scaling from the basal dark area. ‘The apex of wing is shaded with brown and directly below this a short blackish oblique subapical band is present, not attaining however to costa. Fringes dusky whitish at anal angle. Secondaries pale smoky, darker out- wardly. Expanse 15 mm. Holotype—1 38, Ottawa, Ont. (June 5) (C. H. Young), in Canadian National Collection. Paratypes,—2 2’s, Meach Lake, Que. (June 17), Ottawa, Ont. (June 24), taken by same collector. Argyroploce tertiana sp. n. (Fig. 9). Primaries with basal 2/3 purplish-brown, sprinkled with bright brown and with several darker blotches centrally; the beginning of an antemedial pale band is visible in a patch of whitish scaling on costa, partially obscured by brown dots; outer margin of dark area oblique and rather irregular; outer 1/3 of wing white, considerably obscured by dark shading, much more so than in preceding species; three dark dashes along costa; apex of wing dark, shaded with bright brown which continues downward along outer margin; a dark oblique subapical band, not attaining costa and shaded with light brown scales; the space between this band and the dark basal area is almost completely occupied by a broad grayish shade sprinkled with brown, extending upwards from anal angle to a point opposite cell and broadest at its apex which is truncate; a dark terminal line; fringes dusky. Secondaries smoky, paler basally. Expanse 16 mm, Holotype,—1t 8, Ottawa, Ont. (June 25) (C. H. Young), in Canadian National Collection. Allotype-—1 @, Ottawa, Ont. (June 5) (A. Gibson), in same collection. The @ shows more ruddy scaling below apex of wing and the dark basal area 1s continued along costa to include the first costal dash; the secondaries are also darker. I believe these differences are merely sexual. THE CANADIAN ENTOMOLOGIST. 43 Argyroploce buckellana sp. n. (Fig. 10). Allied to the preceding species, especially the @, in type of maculation but distinct in genitalia. Primaries dark brown, shaded with blackish, with inconspicuous whitish antemedian band and outer 4 of wing dark brown with blackish shading and with a few orange scales on inner margin at base; the outer edge of this area outwardly oblique to beyond cell, then perpendicular to inner margin; white antemedian band heavily sprinkled with brown scaling and not well defined; median broad oblique dark band of even width throughout, outer edge rather irregular in outline and attaining inner margin just before tornus, beyond this band the ground color is white but so heavily shaded with purplish- gray as to leave the white area only distinct as a fine border line to the median band and a paler area at tornus; this pale edging forms a slight white comma- mark on the dark margin of median band opposite cell; three whitish geminate dashes on costa before apex, a dark apical spot and a short curved dark sub- apical band; a ruddy-brown terminal line; fringes smoky, mixed slightly with brown and white. Secondaries deep smoky with paler fringes cut by a dark basal line. Expanse 15 mm. Holotype—1 38, Salmon Arm, B.C. (May 28) (W. R. Buckell), in Canadian National Collection. I take much pleasure in naming the species after the collector, Mr. W. R. Buckell, who has through his careful and painstaking collecting added consider- ably to our knowledge of British Columbian Lepidoptera. Argyroploce sordidana sp. n. Size and general maculation of glitranana Kft. but of a much darker appearance, due to the fact that the pale areas between the dark bands are only slightly lighter in color than the bands themselves. Basal area of primaries black, overlaid heavily with brown and ochreous scaling and interrupted by - several bluish-silvery dots; median band similar in color to basal area, in shape much as in glitranana; the paler space between basal area and median band is cefined by two subparallel bands of bluish-silvery spots the included area being scaled with brown, without the underlying blackish color. A triangular anal spot and broad subapical band similar in color to median band, all their edges defined by silvery scaling; remaining areas similar to antemedian band in color. A row of dark spots along costa bordered with pale ochreous and a dark terminal line. Fringes deep smoky, slightly paler below apex. | Secondaries deep smoky. almost black, with pale fringes. Expanse 16 mm. Holotype—1 4, Coliseum Mt., Nordegg, Alta., 6500 feet. (July 12) (J. McDunnough), in Canadian National Collection. Paratyvpes—3 %’s from same locality (July 7, 12, 18). Argyroploce thallasana sp. n. Allied in size and structure to duplex Wlshm. Primaries with basal two thirds dull purplish washed with olivaceous-brown which color forms a faint basal patch and is most prominent as a large irregular patch on inner half of wing, covering the area between anal angle and middle of inner margin. Outer half of wing olivaceous with small brown apical spot and slight brown shading along outer margin. Costa beyond middle with four pairs of pale ochreous 44 THE CANADIAN ENTOMOLOGIST. dashes separated by black and giving rise to irregular silvery-purple lines; from the first pair arise two lines very oblique outwardly below costa then broadening and irregularly perpendicular to inner margin, cutting through the dark patch | and attaining margin near anal angle; oblique streaks from the second and third pairs of dashes coalesce to form a purple stripe which curves and runs sub- parallel to outer margin, bifurcating above anal angle; from outer of the last pair of dashes a short purple streak extends to outer margin below apex defining the brown apical spot. Some pale terminal dots, most evident above anal angle. Fringes mixed pale and smoky with dark basal line. Secondaries smoky with paler fringes. Expanse 22 mm. Holotype—t ¢, Aweme, Man. (June 17) (N. Criddle), in Canadian National Collection. . Paratypes,—2 9’s, Aweme, Man. (June 25); Lauder, Man. (Aug. 1), by same collector. Argyroploce aspasiana sp. n. (Fig. 15). Allied to instrutana Clem. in color and maculation but much smaller. Base of primaries dark olivaceous-brown with considerable white scaling at extreme base; a whitish transverse antemedian band cut by a brown central hair-line; the band is slightly excurved below costa and the edges are rather irregular; median dark band composed of ruddy-brown scaling on a dark ground- color giving a decided olivaceous-brown tinge; the outer edge is strongly out- wardly oblique from costa to centre of wing where it forms a prominent pro- jection and then bends inward to inner margin, the width of band in centre of wing being twice the width of same at costa and inner margin; the apex of the projection is scaled with black; a long narrow triangular brown spot before anal angle and a broad similarly colored oblique subapical band extending from costa to below middle of outer margin and containing a dull leaden patch opposite the cell; intervening pale areas are silvery with scattered white scaling; apex of wing brown, cut by a silvery streak, and with three geminate white streaks at apical portion of costa and a pale line below apex on outer margin. Fringes dusky, slightly cut by brown. Secondaries smoky with paler fringes. | Expanse It mm. Holotvpe,—t &, Mer Bleue, Ottawa, Ont. (July 3) (C. H. Young), in Canadian National Collection. Paratypes,—1t 8, 2 92’s, same locality and collector, (July 2-3). The male genitalia are so different as to almost suggest another generic reference but I can see no other structural differences to warrant this at present. The uncus and tegumen are strongly chitinized and the former is long and pointed; the gnathos is well developed but the socii are lacking. A study of genitalia of series before me from Ottawa, Ont., and Nordegg, Alta.. shows that there are several quite distinct species in the difficult campestrana group which as yet are unnamed. One of these may possibly prove to be glaciana Moesch. but as none of them fits very closely the description and figure of this species (1860, Wien. ent. Monatsschr. IV, 380) and as it is impossible at the present time to get information concerning the genitalia of the type specimen, I venture to propose names for all of these species as follows ;— 1 THE CANADIAN ENTOMOLOGIST. 45 Argyroploce castorana n. sp. (Fig. 12)- Thorax, palpi, head and abdomen black-brown; primaries black-brown crossed by a white antemedian band and with the apical % more or less of the same color. Basal area deep black-brown, the outer edge rather evenly convex with a slight outward projection below cell; white antemedian band with outer ‘edge only slightly irregular and with faint dark central hair-line; median band broad, dark black-brown, slightly suffused with purplish scaling, broadest on inner margin where it is extended to include the triangular anal patch, the outer edge being irregularly concave from costa to above vein 2 and then perpendicular to inner margin just before tornus; on this outer edge in the central area of wing a round blackish spot is more or less distinctly visible, defined on its upper inner edge by a white dot; subterminal area white with a few dark striations and with two black costal spots, separated by white areas through which a fine black hair- line runs; opposite cell is an irregular dark shade which at times connects with the terminal dark area and also with the median band above tornus; apex and outer margin of wing rather broadly black-brown, narrowing to just above anal angle. Fringes smoky, paler at anal angle, with a darker basal line. Secondaries pale smoky with paler fringes which show a dark basal line. Expanse 17 mm. Holotype—t1 8, Nordegg, Alta. (July 7) (J. McDunnough), in Cana- dian National Collection. Paratypes——9 é’s. Nordegg, Alta. (June 24, 30, July 4, 5, 7) (J. Me- Dunnough), in same collection. There is also a series before me from Ottawa, Ont., slightly smaller in size than the Nordegg specimen but with same type of genitalia. The species is best separated from campestrana by the fact that two instead of three postmedian costal spots are present; in this feature it approaches fuscalbana Zell., which, however, besides differing in genitalia, has a brighter and more - contrasted type of coloration. Argyroploce polluxana n. sp. (Fig. 11). Very similar to preceding species but with white areas more silvery-white, giving a more contrasted tone to the coloration. The antemedian white band sends a short rounded projection in the cell into the dark median area, and opposite this is a similar projection from the pale subterminal area ; the triangular spot before tornus is not so entirely merged into the median area but is slightly defined inwardly by pale purplish shading; the subapical oblique streak is also partially separated from the dark apical area by paler purplish shading and at times bends backward towards apex of triangular patch; there are three dark costal spots, and the white subterminal area is more striated and blotched with dark color than in castorana. Expanse 18-19 mm. Holotype—1 é, Nordegg, Alta. (July 5) (J. McDunnough), in Canadian National Collection. Paratypes,—5 4’s, same locality and collector (July 7, 14, 20). The species were taken along with the preceding in a mixed spruce and tamarack swamp. ‘There are a number of specimens from Ottawa, Ont., in the Canadian National Collection which show the same type of maculation and genitalia as the type specimens. 46 THE CANADIAN ENTOMOLOGIST. Argyroploce carolana n. sp. (Fig. 14). Very similar in maculation to the two preceding species but smaller and with a decided olivaceous tinge to the dark areas. In contradistinction to the allied forms the patagia are white with the exception of a dark patch at base, the thorax is also crossed by white bands; on the primaries the outer edge of the basal dark area tends to become irregular, showing (in two specimens) slight rounded excavations in cell and on submedian fold; the outer edge of the dark median band shows a downward indentation of white color at the apex of the triangular patch, which patch is joined to the median area; the subterminal white band is narrow, the whole terminal area being broadly (except at costa and anal angle) suffused with olivaceous brown; there are two olive-brown costal spots which may or may not be connected by hair-lines with the dark terminal area. Expanse 14 mm. Holotype——1 ¢, Ottawa, Ont. (June 21) (C. H. Young), in Canadian National Collection. Paratypes,—1 é, same locality and collector (June 24); 1 2, Trenton, Ont. (June 11) (J. D. Evans) in same collection. The type of genitalia is remarkably distinct. Argyroploce vulgana n. sp. (Fig. 15). Similar in type of maculation to the three preceding species but in the male sex with the pale areas much duller and largely suffused with dark stria- tions. Basal area and median band dull olivaceous-brown, the latter in shape similar to that of castorana and with a fairly evident blackish dot at end of cell: antemedian pale band often very indistinct and at times not attaining inner margin; subterminal pale area reticulate with olive-brown and with two dark costal spots; the dark color of apex and terminal area forms roughly a triangular Slotch of which the outer margin is the base; at times this area can be differen- tiated into an apical blotch and a subapical oblique streak, due to slightly paler scaling between the two component parts; fringes dark at apex, mixed pale and smoky in other areas. Secondaries dull smoky. In the female the white areas are quite prominent and sharply defined. Expanse, 6,15 mm., 2, 14 mm. Holotype. ¢, Nordegg, Alta. (July 9) (J. McDunnough), in Canadian National Collection. Allotype—1 2, Nordegg, Alta. (July 11) (J. McDunnough), in same collection. Paratypes——12 4’s, 1 9, same locality and collector, taken on various dates from June 27 to July 14. The species was quite common in the muskeg around bushes of dwarf birch on which it probably feeds. The type of genitalia is remarkably distinct. Argyroploce nordeggana n. sp. Primaries olivaceous-brown, banded with silvery-white. Basal area dark, the outer edge forming a strong truncate projection in the cell; antemedian band broad, silvery-white with three dark costal dots from central of which a wavy olivaceous line arises, bisecting the band and tending to connect by fine lines with the dark areas on both sides, thus dividing the white area into numerous small ¢ 4 om Se apt ty, THE CANADIAN ENTOMOLOGIST. 47 quadrate patches. Median band dark, upright, rather narrower than usual, almost bisected by projections of the surrounding pale area just above submedian fold, the upper portion with two blunt tooth-like projections on its outer margin ; this dark area is followed by a subterminal silvery band with central dark line arising from costal spot and with same tendency to divide up into small rectangular patchés as in the antemedian band; the pale band bifurcates above anal angle and encloses a large ovate dark spot; the remainder of the wing is occupied by a net-work of olive-brown lines and bands enclosing small patches of leaden-colored scales and containing two geminate white dashes on costa; fringes mixed smoky and white with dark basal line. Secondaries dull smoky. Ex- panse 20 mm. Holotype-——1 6, Nordegg, Alta. (July 14) (J. McDunnough), in Cana- dian National Collection. Paratype,—1 4, same locality and collector (July 18). A female specimen which we are inclined to associate with this species is whiter, especially in the apical area; where the dark bands are reduced and the leaden-colored scales replaced by white ones. A NEW LITHOBIID OF THE GENUS PAOBIUS. BY RALPH V. CHAMBERLIN, Cambridge, Mass. Through Dr. J. McDunnough I have received for identification a speci- men of a diplopod and two specimens of a chilopod collected in Alberta, Canada, by Mr. N. B. Sanson of Banff. The diplopod is apparently a not fully mature male Parajulus hewitti Chamberlin, a species described originally from speci- mens taken by Dr. Hewitt at Agassiz, B.C. The present specimen is much darker in color than the type, with the legs nearly chestnut. The cauda is very similar though somewhat shorter and the lateral striae are more pronounced. It was taken nearing Bryant Creek Cabin, Sept. 22, 1921. The chilopods represent a new species in the genus Paobius of the family Lithobiidae. In the key to species given by the writer in his review of the genus* the present species runs out to P. orophilus Chamberlin, a British Columbian species from which, however, it is clearly distinct. The key may be modified to take in the new form as follows: a. Dorsal spines of anal legs I, 0,3,0,0 or I, 0, 2,0, 0. b. None of the posterior coxae laterally armed; ventral spines of thirteenth legs 0, I, 3, 3,1; third joint of first ten or more pairs of legs with but two dorsal spines..... SE git i re Me ee P. vagrans Chamb. b.1 Last two pairs of coxae laterally armed. Ventral spines of thirteenth legs 0, I, 2,3, 2 or 0,0, 2,3, 2; third joint of all legs with three dorsal SR Narn scot sat are etre Sheree a hc x ark A Hace eee ws ™ 5 P. boreus Chamb. a.t Dorsal spines of anal legs I, 0, 3,1, 0. b. Dorsal spines of penult legs 1,0, 3,1,1 ........-- P. albertanus, sp. nov. b.t Dorsal spines of penult legs 1, 0, 3, 1, 0. *Bull, Mus. Comp. Zool., 1916, 57, p. 162. 48 THE CANADIAN ENTOMOLOGIST. c. Fifth joint of sixth to ninth pairs of legs with but one ventral spine; head equal in length and breadth; claw of genital forceps of female ripagitie .. oo} oes ce et oe ee eee P. columbiensis Chamb. c.! Fifth joint of sixth to thirteenth pairs of legs with two ventral spines; _ head wider than long; claw of genital forceps of female bipartite a ee ee ey ee Sele in P. orophilus Chamb. Paobius albertanus sp. nov. Dorsum brown oi a slightly chestnut cast, the head similar, typically with a darker spot on posterior half. Head slightly wider than long. Ocelli in three series, nine to twelve in number. Antennae rather long; articles all relatively long. the last one equal in length to the two preceding ones taken together. _Prosternum and its teeth much as in P. orophilus; the distance between chitinous spots similarly four times as long as the dental line. Ventral spines of penult legs 0, I, 3, 3,2; dorsal spines, I, 0, 3, 1, 1; claws three of which the anterior is straight and spine-like. Ventral spines of anal! -legs 0,1, 3,3,1; dorsal spines 1,0,3.1,0; claw single. Last four pairs of coxde laterally armed. Claw of female genital forceps distinctly tripartite; basal spines pro- portionately broad as in P. vagrans, the inner on each side smaller than the outer. Length of male, 9 mm.; of female, 11 mm. Locality —Canada: Alberta. One male and one female taken by N. B. Sanson “the Spring Le trip” April 25 and 26, 1918. Differs from all the previcusly known species in the spining e the penult legs. NOTE ON TYPES OF ERNESTIA R. D- (DIPTERA) BY J. D. TOTHILL, Entomological Branch, Ottawa, Ont. The type of Ernestia nigrocornea Tothill is in the California Academy of Sciences and not in the Canadian National Collection as stated by the author in Canadian Entomoligist, 1921, p. 228. Great Falls, Va., is the type locality of E. platycarina Tothill (1. c¢. p. 271) and the number of the type is 24357 and not 24359. Lillooet, B. C., is the type locality of E. sulcocarina Tothill (1c. p. 272). Bear Lake, B. C., is the type locality of E. bicarina Tothill (1. c. p. 272). Che Canadian Cntomolanist Vow. LIV. ORILLIA, MARCH, 1922. No. 3. POPULAR AND PRACTICAL ENTOMOLOGY Insect Foop oF THE BLAcK BEAR (Ursus AMERICANUS). BY N. K. BIGELOW, _Dept. of Biolegy, University of Toronto During the summer of 1921 the writer of this article was studying the Plankton of Lake Nipigon, Ont., and collecting insects during his spare time. ° While searching for insects in the bush many opportunities were presented for observing the habits of wild life under natural conditions. Not the least interest- ing of these observations were those concerning the Black Bear (Ursus americanus ). On the afternoon of August 22 Duncan Bell, a missionary to the Ojibway Indians of that vicinity, and myself saw a black bear in the bush about one - mile south of Grand Bay. The animal was a small one, only one-third grown, and was walking along a moose trail at a leisurely pace. We walked along the trail in the direction opposite to that taken by the bear and found that the creature had been making a meal off a nest of yellow-jackets only a few minutes previously. Within a very few feet of the spot where we saw the bear we - found the evidences of his repast. |The animal had eaten paper, larvae and adults as well. All that was left was a hole in the ground beside the trail with about half a dozen very angry hornets flying around it. Within fifty feet of this we found where another nest of these insects had been destroyed. In both instances a few of the hornets were still flying about. They proved upon capture to be Vespula diabolica De Saussure. In this same vicinity we found the dung of this or a similar sized bear. This material was apparently a day or two old and was composed of the remains of hundreds of adult hornets some of which were in a good enough state of preservation to be readily identified. Both Vespula diabolica De Saussure and Vespula consobrina De Saussure were present. At this point it may be well to notice what others have to say concerning the bears’ fondness for hornets, Lockwood! tells us in the Riverside Natural ‘History that “Bears like the larvae of wasps’ nests. Such a nest in the ground they will scratch up, digging with much rapidity, but often having to stop from the stings of the enraged insects. They will snarl and roll on the ground and go at it again. Although the punishment is severe Bruin keeps at it until he has secured his hard earned prize.” Ernest Thompson Seton? says that “A pleasing variation of late summer foods is found in the nests of several species of wasps as well as of wild bees.” Wamuel Lockwood, The Riverside Natural History, Vol. V, p. 378. 2Ernest Thompson Seton, Life Histories of Northern Animals, Vol. II, p. 1082, 1083, 50 THE CANADIAN ENTOMOLOGIST. He also states that ‘““According to Merriam the bear digs out the nests of the yellow-jackets devouring both the wasps themselves and the comb containing their honey and grubs.” Bears are very fond of tearing decayed stumps and logs to pieces in search of beetle larvae and ants’ nests. | Remains of their handiwork were found almost every day in the bush. The thoroughness of their search is attested by the minute fragments into which the wood is clawed. The bears’ fondness for ants is well known to the Indians, trappers and fishermen of Lake Nipigon. Professor B. A. Bensley of the University of Toronto has made an interesting observation concerning the bears’ fondness for ants. He opened the stomach of a small bear which he had killed near Go. Home Rivér, Georgian Bay, about the middle of July, 1911, and found it to contain at least a quart of ant pupae. He says that the pupae alone constituted by far the greater part of the material although a few adult ants and small bits of wood were present. This was at a time when the animal could have secured plenty of blueberries if it had chosen to do so. Ernest Thompson Seton? gives us the following interesting information as to the black bears’ fondness for ants. ‘Throughout the summer all kinds of insects and especially ants are important bear food.” y “In the sand hills about Carbury, in the woods about Lake Winnipegosis, throughout the Bitter root mountains of Idaho and in the ranges of the upper Yellowstone as well as in the Rockies of the Colorado and the Low Laurentians of the Ottawa I have found that ants’ nests furnished the bear with an important article of food.” “Following the trail of one I have found that it invariably turned over every log and flat stone that it came to and ripped open every rotten log and stump in its search for insects, the greater part of which must have been ants. Among the Bitter root mountains I have in a single day passed hundreds of these demolished logs and stumps.” “In the Adirondacks according to Merriam the black bear delights in tearing up old logs and stumps in search of the ants that make their homes in such situations.” “While fishing in the North Bay of Big Moose Lake during the summer 1881 Mr. Harry Burel Miller of New York City heard a bear tearing down an old stump that stood on a point in the bay. His guide, Richard Crego, noise- lessly paddled him to the spot and he killed the bear with one ball from his rifle. Its stomach contained about a quart of ants and their eggs.” Stone and Cram,? after telling of the bears’ fondness for berries of many kinds, particularly blueberries, says that “They also dig for roots and bugs and catch grasshopers and crickets in the grass. | When there is plenty of such to be had they will, it is said, pass the newly killed carcass of a deer or sheep without noticing it.” 3Stone and Cram, Amerécan Animals, p. 258, z $ : f : 7 ; io Pe THE CANADIAN ENTOMOLOGIST. 51 A REVISION OF THE NORTH AMERICAN SPECIES OF MORDELLA 2 RELATED TO M. MELAENA. (COLEOPTERA). BY EMIL LILJEBLAD, Chicago, Illinois. In the course of the writer’s detailed study of the American Mordellidae, in which he has had the opportunity of examining many hundreds of specimens of the genus Mordella, it has become apparent that the species comprising the melaena group are insufficiently distinguished by the brief diagnoses heretofore published. This is notably true of MW. melaena and M. atrata (“‘scutellaris’), which the writer has found more or less confused in nearly every collection examined. Five species of this group are recognized from eastern North America, namely guadripunctata, melaena, atrata, lecontei, and a new species, M. knulli, from Florida. Of the five characteristically western species here discussed, four are described as new, and the fifth, M. signata, is recorded for the first time from the United States. 1. Mordella signata Champion.? The two specimens at hand, identified as of this species, are the first to be recorded north of Middle America. Both were taken in New Mexico, one in Socorro County, by Mr. W. J. Gerhard (deposited in the Field Museum of Natural History), the other at Del Labo (in the writer’s collection). These two differ slightly from the types as originally described, but as Champion cites two “variations,’ one from Mexico, it seems probable that these slight variations in coloration are not of specific significance. This is a large and well-marked species. Form cuneate. Head black, with cinereous pubescence; prothorax black, with yellowish cinereous pubescence becoming denser on the sides; elytra with the ground color ferruginous, darker toward the apex, marked with a rather broad oblique line from the humeral angle downward one-third length of elytra to near the suture, then forward along the suture to base, and also with an equally broad transversely lunate mark on the disc beyond the middle elytra, with yellowish-cinereous pubescence. Anal style short, bluntly rounded at apex. Length, 8 mm. to end of elytra, 10 mm. to end of anal style. 2. Mordella quadripunctata Say. This, one of our largest species, is rather rarely found in collections. The writer, however, has been able to examine specimens from many localities— Maine, Canada, Virginia, West Virginia, Iowa, Kansas and Colorado. In some specimens, particularly miales, the subsutural spots are but faintly indicated. The presence of the two pair of spots, however, best distinguishes this form from melaena and atrata; it is, furthermore, more robust and usually longer. Body cuneiform, robust. Color black, entirely covered with sericeous- brownish-cinereous pubescence, more coarsely on the head and thorax than on the elytra; scutellum with silvery-white pubescence; elytra each with two cinereous-argenteous spots, rather beyond the middle, the larger exterior and somewhat linear, the smaller one obsolescent, subsutural, near the base; lower 1Biol. Cent. Am., IV, 2, 1891, p. 276. 2 THE CANADIAN ENTOMOLOGIST. gi parts with argenteous pubescence at the sides of the abdominal segments. Head ~ minutely punctured. Last joint of the maxillary palpi scalene-triangular, the inner side a little longer than the apical. Antennae short, reaching middle of thorax; the four first joints small; the fifth to eleventh clavate; third and fourth - joints about equal in length; fifth a little longer than the sixth and nearly twice as wide at apex; sixth to tenth about equal in length, clavate, forming an — elongated club; eleventh one-third longer than the tenth, tapering to apex. Eyes moderately large, finely granulated. Prothorax one-third wider than long, very little broader than the elytra at base, evenly rounded and converging to apex, the hind angles obtuse; its surface finely punctured; base of prothorax broadly rounded in front of the triangular scutellum. Elytra more coarsely punctured, with two faintly indicated costae extending from base to slightly beyond the middle. Anal style short, stout, truncate at tip. The inner edges of the femora of the anterior legs bear long setae in the male, only fine pubes- cence in the female. Length to end of the elytra, 6-7 mm.; to tip of the anal style, 7-8 mm. ff, 3. Mordella melaena Germar.? Mordella melaena is also one of our rarer species, being usually found singly. Specimens have been seen by the writer from Canada, Maine, Massachusetts, New York, Virginia, Michigan, Illinois and Iowa; it has been recorded further from Pennsylvania, Georgia, Tennessee, Ohio and Colorado. This species appears most closely allied to M. quadripunctata, but may readily be distinguished from it, as indicated above in the account of that form. Care must be taken to avoid confusion of this species with M. grandis, which it closely resembles; in that species however, the antennae are much longer, more serrate, and less clavate, and the suture has more or less silvery pubescence. The same characters also differentiate melaena from two smaller western species, albosuturalis and hubbsi. The best character by which melaena may be separated from atrata is the form of the antennae, which are more clavate, the outer joints being more dilated and compact, rather than serrate; further, the scutellum is more sharply triangular, and the anal style is always short and blunt at the tip, not long and slender. Form robust cuneiform. Color black, the upper surface entirely covered — with fine sericeous-brownish-cinereous pubescence (nearly black in some speci- mens); base of the anal style with cinereous pubescence; lower parts black. with cinereous-argenteous pubescence at the sides of the abdominal segments. Head comparatively large, minutely punctured. Last joint of the maxillary palpi scalene-triangular, more rounded on the inner angle in the female than in the male. Eyes moderately large, finely granulated, rounded in male, more oval in the female. Antennae with first to fourth joints slender; fifth to eleventh strongly serrate, or nearly clavate, forming an elongated club; third joint a ~ little longer than the fourth, which is a little the broader at apex; fifth one- fourth longer than the sixth; sixth to tenth equal in length; eleventh longer than the tenth, triangular, rounded on the inner and apical angles. | Prothorax one- third wider than long, rather finely punctate, widest little before the base, evenly 2Ins. Spec. Novae, Halle, X XIV, 1824, p. 169. THE CANADIAN ENTOMOLOGIST. 53 rounded and converging to apex; its base at middle, in front of the triangular scutellum, broadly rounded. _Elytra a little narrower at base than thorax, the sides at middle slightly sinuate, and tapering to apex. Anal style short, and rounded at tip. Length to end of the elytra 5-6.5 mm., to tip of the anal style 6-7.5 mm. _ 4. Mordella atrata Melsheimer. This is the species which has ordinarily been named Mordella scutellaris. But since Fabricius® states in the original description of scutellaris that the head and thorax are ferruginous, or rusty-red (Caput et thorax ferrugineo paullo nitidula) and the elytra black, and gives as the type-locality South America, whereas in the present North American species the color is wholly black, with gray or brownish pubescence, the writer can not agree in regarding as available the name scutellaris. The oldest tenable ne‘ne for the North American species here discussed appears to be Mordella atrata* for it best agrees with Melsheimer’s original account of atrata. | Numerous specimens have been examined from Canada, Maine, Connecticut, Pennsylvania, Vermont, Massachusetts, New York, New Jersey, Maryland, North Carolina, Colorado, Florida, Tennessee, Michigan, Ohio, Indiana, Illinois, and Iowa. Body cuneiform, more robust in female than male. Color black; the pubescence of the upper surfaces brownish or very slightly cinereous; of the scutellum cinereous; of the lower parts brownish, sometimes nearly black : sides and anterior margin of the abdominal segments and base of the anal style with sericeous-cinereous hairs. Last joint of the maxillary palpi scalene-triangular in the male, the inner angle rounded in the female. Antennae with joints one to four slender; fifth to tenth serrate; third joint a little longer than the fourth; the fifth, triangular, one-third longer than the third and twice as broad at apex; sixth, one-third shorter than the fifth; seventh to tenth of uniform width, serrate, about as broad as long; eleventh constantly very little longer than the tenth and rounded on inner side. Eyes moderately large, and rounded (particularly in males). Prothorax a little broader than the elytra at base, widest little before the base, then evenly rounded to apex. Scutellum broadly rounded at tip. Anal style rather long, gradually pointed and about one-third longer than thorax. In some specimens from Maine and Massachusetts the anal style is a little shorter and broader at base, tapering abruptly to the middle, then maintaining its width to the apex. Length to end of the elytra 3.5-4.5 mm., to end of the anal style 5.5-6.5 mm. 5. Mordella lecontei Sciki. This apparently valid species has passed currently, under the preoccupied name of M. irrorata LeConte®, as a synonym of Mordella “scutellaris” (=atrata). It differs markedly from that species, to which it is doubtless closely related, in color. The head and thorax are rather closely covered with black and brownish or grayish brown pubescence, the elytra with black pubescence, sparing- 8Syst. Eleuth. II, 1801, p. 123. 4Proc. Acad. Nat. Sc. Phila. II, 1846, p. 313. Junk, Col. Cat. pars 63, 1915, p. 23. ®Proc. Acad. Nat. Sci. Phila., XIV, 1862, p. 46, Trost, Kleine Beytr. 1801, p. 27. Sturm, Cat. 1843, p. 170. ' 54 THE CANADIAN ENTOMOLOGIST. ly but conspicuously sprinkled with single shining cinereous, or sometimes — brown, hairs. This species appears to be particularly abundant in Pennsylvania and Maryland. Other specimens have been examined from Massachusetts, Maine, Georgia, West Virginia, Ohio, Indiana, Illinois, Wisconsin, Iowa, North Carolina and Texas. Body cuneate. Head and thorax rather closely covered with black and brownish or grayish-brown pubescence. Elytra with black pubescence, sparingly sprinkled with single shining-cinereous, or sometimes brown, hairs. | Otherwise the species resembles Mordella atrata. 6. Mordella albosuturalis, sp. nov. This species somewhat resembles Mordella atrata, from which it differs in having silvery pubescence along the base and suture of the elytra, and the outer joints of the antennae slightly tapering to apex. It seems only to occur in the western States. It has been taken on flowers of Heteromela arbutifolia and several composites. Body cuneiform, the male usually narrower than the female. Color black, with fine reddish brown pubescence; basal margin of thorax and elytra, the scutellum and elytral suture with argenteous pubescence; under-parts with cinereous pubescence, most dense on the sides and anterior margins of the ventral segments. Last joint of the maxillary palpi scalene triangular in the male, the inner angle more rounded in the female. Antennae with joints one to four slender ; the fifth to tenth joints serrate ; the third and fourth equal in length, the fourth the widest; fifth about equal in length to the fourth, but one-third broader at apex, with sides straight; sixth to tenth serrate, with inner sides rounded, the sixth broadest; those following diminishing slightly in width to the tenth; eleventh joint one-third longer than the tenth, more oval in shape. Eyes elongate-rounded or egg-shaped, sinuate on the upper side near the antennal cavity in the male (this sinuation nearly obsolete in the female). | Prothorax very little wider than the elytra, broadest near the base, then evenly rounded to apex, its base in front of scutellum broadly rounded. Scutellum triangular, rounded at apex, in the male usually a little narrower than in the female; anal style long, gradually tapering in the male, wider and more abruptly tapering to middle in the female. Length to end of elytra 4-5 mm., to tip of anal style 5-5-6 mm. Several hundred specimens have been examined from California, and some from Oregon, Nevada, Idaho, Montana and North Dakota. The male holotype and female allotype is from Callistoga, near Mt. St. Helena, California, collected on July 14, by C. L. Hubbs. | Paratypes were collected by Mr. Hubbs at the type locality, and at the following other localities, all in California; Mt. Diablo, fuly 18; Blue Lakes, July 12; Carmel, June 18; Jamul, San Diego County, June 10, and Healdsburg, July 10. | Other paratypes from California are as follows: Tule River, July 30 (F. S. Daggett) ; Mariposa Co., June 2-17 -(F. W. Nunenmacher) ; Paradise Valley, August 15 (J. C. Bradley) ; Paradise Valley, Kings River, July 15 (R. L. Beardsley) ; Sugar Pine, Madera Co., August 24-31 (J. ©. Bradley); Hockett Meadow to Sequoia National Park, July 25; Los is (Pet Nee 408 THE CANADIAN ENTOMOLOGIST. 55 Gatos Canyon, Fresno Co., June 6-8 (J. C. Bradley) ; Felton, September 6 (J. C. Bradley) ; Switzers Trail, St. Gabriel Mt., July 1ro-11 (Fordyce Grinnell, jr.) ; Camp Baldy, Los Angeles Co., July 28 (L. L. Muckmore); Mt. Lowe, June; - Tulare Co., July 30; Raymond, May; Palmas Spring, May 29 (C. A. Frost, collection) ; Giant Forest, Sequoia National Park, July 21-26 (J. C. Bradley) ; Sherwood, Mendocino Co., July 1 (Cornell University Collection). Still other paratypes are from Josephine Co., Oregon (June 11, F. W. Nunenmacher) ; Esmaralda Co., Nevada (June 29, F. W. Nunenmacher) ; Troy, Idaho, (August 16, Wm. Mann) ; Glen, Montana, (C. C. Adams) ; and Bottineau, North Dakota, (August 1, T. H. Hubbell). 7. Mordella hubbsi, sp. nov. 1 This species differs from the other black forms of the genus in the ferruginous color of the femora of the posterior and middle legs, and can easily be distinguished by this character. All of the known specimens have come from California. Cuneiform, especially in the male. Color iridescent black; head and thorax with sericeous-cinereous pubescence; elytra with fine reddish-brown pubescence ; basal margin of thorax, scutellum and elytral suture with argenteous pubescence ; under-parts with cinereous pubescence, becoming more silvery at the sides of mesosternum and abdominal segments; mouth-parts and femora of the anterior and middle legs ferruginous to near the knee; antennae dull red at base; last joint of the maxillary palpi scalene-triangular in male, more rounded~ on the inner angle in the female. Antennae with joints one to four narrow; the fifth to tenth serrate; third joint one-third longer than the fourth; fifth to tenth, as wide as long, the fifth broadest, the sixth to tenth slightly decreasing in width; eleventh little longer than the tenth, oval. Eyes rather large, rounded and sinuate in front in the male, more oval or egg-shaped, with scarcely any sinuation in the female. Prothorax much wider than the elytra at base, widest basally and evenly rounded, converging to apex; its base in front of scutellum broadly rounded. Scutellum triangular, rounded at tip. Anal style long, blunt at tip, about one half as long as the elytra. Length to end of the elytra, 3.5-4.5 mm.; to tip of the anal style 5-6 mm. Forty-five specimens examined. ‘The male holotype and female allotype, from Carmel, California, were collected on June 18, by C. L. Hubbs. — Para- types are from same place, and from Switzer’s Trail, St. Gabriel Mt., California (June 10-July 14, Fordyce Grinnell, jr.) ; Tulare Co., California (July 30, C. A. Frost) ; Long Canyon, California, June 3; Mariposa Co., California (June 5-17, F. W. Nunenmacher); Paradise Valley, Kings River, California (July 15-18, R. L. Beardsley) ; Kenworthy, California (June 8, C. A. Frost); Sher- wood, Mendocino Co., California (July 1, Cornell University collection) ; Three Rivers, Giant Forest, Tulare Co., California (July 16, J. C. Bradley) ; Coalinga, Fresno Co., California (June 1-3, J. C. Bradley) ; Camp Baldy, Los Angeles Co., California (July 28, L. L. Muckmore) ; Los Gatos Canyon, Fresno Co., Cali- fornia (June 6-8, J. C. Bradley) ; Raymond, California (May), and St. Gabriel Mt., California (June 5, C. A. Frost, collection). 56 THE CANADIAN ENTOMOLOGIST. This species I dedicate to my friend, Carl L. Hubbs, from whom I have received many rare specimens and other assistance, and I hope may be considered a valid species for all time. 8. Mordella grandis, sp. nov. This species might readily be confused with Mordella melaena, on account of its size and general appearance. It can best be separated from that species by the form of the antenna, which is longer, more narrow (not clavate), and slightly tapering to apex from the sixth joint, and by the silvery sutural line, and the longer and more narrow anal style. It is also closely allied to albosuturalis, but is more robust, the antennae are longer, and the scutellum is more triangular. A rather large species, of cuneate form. Color black; pubescence of the upper surfaces very fine, sericeous black, with cinereous or brownish hairs intermixed; scutellum and elytral suture with argenteous pubescence; lower parts cinereous, the sides of breast and abdominal segments more strongly argenteous pubescent. Last joint of the maxillary palpi scalene-triangular in male, more rounded on inner angle in the female. Antennae with joints one to four narrow, the fifth to tenth serrate; the third slightly longer than the fourth, which is a little wider at apex; fifth to tenth, each a little longer than — broad, the sixth widest; the following joints slightly diminishing in width to the — tenth; eleventh longer than the tenth, oval in shape in the male (in the female the fifth joint is a little longer than the sixth, the sixth to tenth are about as. wide as long). Eyes in male large, rounded, sinuate in front; in the female, more oval in shape, and less sinuate. Prothorax wider than long, considerably wider than the elytra at base, widest near the base, and evenly rounded to apex, hind angles subacute, the base in front of scutellum broadly rounded. Scutellum large and triangular, more pointed in female than the male. Anal style as long as the thorax, truncate at tip. Length to end of the elytra 4-5.5 mm.; to tip of the anal style 6-7 mm. Eighteen specimens examined from California and Oregon. The male holotype and female allotype are from Mariposa County, collected on June 5, by F. W. Nunenmacher. The paratypes are from same place, and from Tulare Co., California (July 30, C. A. Frost); Long Canyon (June 3); Los Gatos Canyon, Fresno Co., California (June 6-8, J. C. Bradley) ; Sherwood, Mendocino Co., California (July 1, Cornell University collection) ; Camp Baldy, Los Angeles Co., California (July 28, L. L. Muckmore) ; Paradise Pk., Kings ‘River, California (July 18, R. L. Beardley); Sonoma Co., California (Cornell Uni- — versity) ; Kaweah, California (R. Hopping) ; and Pendleton, Oregon. 9. Mordella brevistylis, sp. nov. This species somewhat resembles Mordella atrata, but is readily dis- tinguishable by its more elongate form and the shorter, blunt anal style. Form subcuneiform. Color black; both upper and lower surface with black or dark reddish-brown pubescence; sides of breast, and first and second abdominal segments at sides with cinereous pubescence. Last joint of maxillary palpi scalene-triangular. | Antennae short, reaching to about middle “ PO 8p 0 tint Re ae ee ee a ee ee eee ee eT », / tage TaN eget, © oe a i : b A %. e+ a ‘aay Pin Ret My Tet hex = an , THE CANADIAN ENTOMOLOGIST. 57 of thorax. Antennal joints one to four narrow, the fifth to tenth segments serrate ; the third and fourth equal in length, the fourth widest; sixth to tenth about as wide as long, nearly alike in shape; the fifth with the sides straighter ; _ the eleventh oval, a little longer than the tenth. Eyes large, rounded, very _ little or not at all sinuate in front. Prothorax very little wider than the elytra . at base, one-fourth wider than long, widest a little before the base, then evenly rounded to apex; base of thorax in front of scutellum nearly truncate or very slightly emarginate. Scutellum triangular, broadly rounded at apex. Anal style short, shorter than the thorax, and blunt at tip. Length to end of the elytra, 4.25 mm.; to end of the anal style, 5.25 mm. a Four specimens examined, presumably females, from New Mexico, labelled Cornell University, Crew Collection. |The type is deposited in the Cornell University collection; paratypes are in the possession of the writer. 10. Mordella knulli, sp. nov. This large and very interesting new species of Mordella is known from only one specimen, presumably a female, collected on June 20, at La Belle, > Florida, by Mr. J. N. Knull, to whom it is dedicated. It is entirely different in markings from any other North American form of the genus, differing particularly in the distinct silvery pubescent markings on the whole upper sur- face. On account of its size, it is suggested that this species be placed in taxonomic sequence after Mordella quadripunctata. Cuneiform. Ground-color black. Head densely covered with fine argent- eous pubescence, except on a large median triangular spot, where the pubesence is less dense, showing through the black ground color; antennae and palpi black; eyes dull yellowish, transparent, with ocelli and margin black; prothorax with _all the margin, except the median third of the apical margin, an angulated band, one third from apex, reaching the side margins, a streak in the middle from apex downward to the middle band, and a streak each side the middle, fronr the “middle band downward not quite reaching the base, with argenteous pubescence (leaving five large spots with black pubescence); scutellum with argenteous pubescence ; elytra each with a curved band, from the scutellum outward and downward to about one-third from the base, and then extended outward to the side margin, (leaving a somewhat cordate back spot in the middle of the two elytrons, and a somewhat elongated black spot at the humeral angle) a round spot on each elytron in the middle, very close to the suture, a sutural streak from near the base, slightly widened’ to one fourth from apex, where it is connected with an oblique triangular band, which reaches the margin, with argenteous pubescence, for the rest covered with black pubescence; under parts black, densely covered with argenteous pubescence, except for a black spot on the posterior margin on the sides of meso and metasternum; a similar denuded spot near the hind coxal plate, and the posterior side margin of the abdominal seg- ments; legs with argenteous pubescence on femora and outer margin of tibiae and tarsi; anal style black, with a little argenteous pubescence near the base. Head rather large, somewhat triangular in shape, finely punctured; antennae . " ~ > a Pp 8 THE CANADIAN ENTOMOLOGIST. cn not reaching the base of thorax; joints one to four narrow; fifth to tenth serrate; third and fourth joints equal in length; fifth one-fourth longer than the fourth, and much wider at apex; sixth one-fourth shorter than the fifth; seventh to tenth about equal in length, slightly decreasing in width; eleventh a little longer than the tenth, rounded on the inner angle. Eyes large, obovate, finely granulated; maxillary palpi scalene-triangular. Prothorax one-thir}l wider than long, finely punctured; basal lobe in front of scutellum broadly rounded ; sides feebly rounded and converging to apex, the anterior and posterior angles acute; scutellum triangular. Elytra more than twice as long as wide, finely punctured. Tibia of the middle leg longer than all the tarsal joints of the same leg. Anal style long, pointed. Length to end of the elytra, 7.5 mm.; to tip of the anal style, 10 mm.; breadth, 3.5 mm. The single type specimen is placed in the writer’s collection as a gift from Mr. Knull. SOUTH AMERICAN GLENURUS AND SOME OTHER MYRMELEONIDAE. BY NATHAN BANKS, Cambnidge, Mass. A striking new species of Glenurus from Bolivia has induced me to review the other species from South America, and I give below a synoptic table to all the forms except one recently described by Navas. Recently Mr. Peter- sen has furnished me with some photographs of certain types of Gerstaecker, and from these I learn that a species I had considered the G. psilocerus is not that but new. 1. - Front wings without the large dark apical mark.............. heteropteryx. Both wings:-with large dark apical marks. 5.<..... ©. ..4. . (yee a 2. In the front wings the space before the apical mark contains many dark SPOS oy. Foe ae tte 6 cP aA) Sh ck os ee ie aa er croesus. In front wing this space largely clear... 2. .... 5. 2... 3.on- oe 3. 3. Dark mark of hind wings with two pale spots..................- peculiaris. Dark mark of hind wings with but one pale spot...............e2ce--+% 4. 4. In hind wing the apical pale spot is indented by the dark; the dark mark of fore wings has the inner edge lobed, and notched behind.......... incalis. In hind wings the apical pale spot is not indented by the dark; the dark mark of fore wing is not lobed on the inner edge, and not notched be- Bind, 6 oc |. . Tigers ate b cies aeitans See tlre cory he pe eee luniger. The Glenurus discors Navas agrees with heteroptery.x, but is said to lack the white in hind wing at tip, and to have shorter hind wing; but this latter character is variable. Glenurus incalis sp. nov. In appearance and markings very near to G. peculiaris. ‘The wings are rather more slender. The fore wings have the apical mark shaped like that of G. peculiaris, except that it is notched behind; the pale area beyond is more uniformly pale, with but two or three dark spots, of a milky and even faintly ery bea tk "Ss mi ens Pay Re ‘in?” THE CANADIAN ENTOMOLOGIST. 59 pink appearance as in our G. gratus. The apical mark of the hind wing is fully as long as in G. peculiaris, but with only one pale spot behind, and the apical pale spot is indented by the dark from near tip. Body and legs marked as in G. peculiaris. Expanse, 84 mm. From Chachamayo, Peru, Nov. Type, M. C. L., 12030. Glenurus croesus sp. nov. In general resembling G. peculiaris. The body is deep black, with a pale median line on the pronotum; the legs are yellowish, not dotted nor marked with dark, except that the tarsi are darker. The fore wings have the apical mark much as in G. peculiaris, lobed internally but less oblique; the pale band is not as much broken as in G. peculiaris. The space before the apical mark contains many dark spots, somewhat in rows, that near the end of the anal is very large and enlarged above. The hind wings have the apical mark hardly as long as in G. peculiaris, with but one pale spot on the hind border, and that much narrowed behind. Wings rather shorter and broader than in G. peculiaris. Expanse, 72 mm. From the Province of Sara, Bolivia, 450 m. Type, M.C.L., 12031. Glenopsis petersensi sp. nov. Pale yellowish; a black band below and one above the antennae; vertex with two dark submedian spots; antennae dark, annulate with pale, tip darker. Pronotum faintly marked with dark streaks each side, more or less connected -with two submedian lines; thorax with pale and dark patches, not very clear; the scutelli with a pale median stripe; pleura with a few dark spots; abdomen with dark spot at base and tip of each segment, behind the dark more extensive. Femora with dark dots and apical bands, tibia with sub-basal and apical dark bands, tarsal joints dark at tips. | Wings hyaline; venation mostly white, with some brown streaks and cross-veins; two small brown clouds near end of cubitus, and an oblique mark above end of the -anal vein, the upper end the larger; some of the marginal forks brown, or with brown spots. In the hind wings some of the veins partly or wholly dark, no clouds; stigma of both pairs white. In structure very similar to G. anomala, but the hind wing is scarcely, if at all, longer than the fore wing. Expanse, 83 mm. From Chachamayo, Peru, Nov. eype, M,C. L., 12044. I had identified this as probably the G. psilocerus of Gerstaecker, but Mr. Petersen, to whom I sent a specimen, said that it is different, and kindly sent me a photograph of Gerstaecker’s species, which is hardly more than a variety of G. anomalus. 60 : THE CANADIAN ENTOMOLOGIST Austroleon latipennis sp. nov. Face pale, a dark indented mark below the antennae; vertex mostly brown, a faint pale transverse line in front, and about three pale spots behind; antennae brown, annulate with pale; pronutum with two broad brown sub- median stripes; rest of thorax pale, with four rows of spots, or interrupted - stripes; pleura with many dark marks; abdomen dark below, above pale, with a median dark line; legs pale, front femora above and tips of tarsal joints dark. Wings hyaline; veins pale, with dark spots at joinings of veins, gradates and marginal forkings brown; median vein plainly marked; hind wings much less marked, except subcosta and radius. The wings are very broad, especially : toward the tip, as in A. stictogaster, and the tips acute and almost sinuate behind. Expanse, 43 mm. : From Chapada, Brazil (H. H. Smith). i ype, Me Co 1,5 12032. Z Differs from A. stictogaster in markings; related by marks to 4. argentinus, but differs by very broad wings. ‘ Hesperoleon tripunctatus sp. nov. In general appearance very similar to H. sackeni; the abdomen has the same pale spots, but those on the posterior half are plainly longer and broken by dots and streaks, and there is white hair on the pale spots of all the segments. The face, instead of the two oblique spots of sackeni, has a large black interantennal mark, reaching below the antennae and there nearly straight across. The vertex is fully as high as in sackeni, and has a band in front and behind two submedian, and farther back a median dark mark. The pronotum has three dark stripes, not reaching in front of the transverse furrow, the median one broader behind, and there including a pale spear-mark; neat the front margin are four faint, dark spots. The thorax is spotted with pale and dark much as in sackeni, but on the mesoscutellum are three very prominent shining black spots along its hind border, each on an elevated area; on the metascutellum the apical median spot is also shining black and elevated. The pleura are pale, spotted with dark. The legs are marked much as in sackeni, with long white and some black bristles; the fine hair is mostly black. The 2 wings are marked very much as in sackeni, and the venation is generally similar, with a wide apical area, but the radial sector arises more basally, and there is but one series of cells between the cubitus and the anal in the fore wings. lhe male genitalia are extremely short, and not at all extended, less than one-half as long as the last segment, but there is a lobe below at base as in sackent. Ixpanse, 48 mm. From Palmerlee, Arizona, June, July, (Biederman). ivpe, MOC. L.; 12048 Readily separated from H. sackeni by the three shining black spots on the Mesocutellum. THE CANADIAN ENTOMOLOGIST. O1 ON THE GENUS ELIDIPTERA SPIN. (HOMOPTERA) BY F. MUIR, Hawaiian Sugar Planters’ Experiment Station, Honolulu, T. H. Elidiptera Spino-a 1839, Ann. Soc. Ent, Fr. viii, p. 304. Logotype, callosa Spin. Among some Homoptera forwarded to me by Mr. C. B. Williams from Trinidad is a specimen that I at first considered to be a new genus near to Achilus but later identified as Elidiptera callosa Spin. or a very closely allied species. I was acquainted with this genus by species from North America and the West Indies and so failed to recognize callosa as belonging to it. The genus was erected for callosa and some other species and was illustrated on plate 15, figures 2, 3 and 4 of the same work. ‘The figures indicate that callosa differed from the other two species, advena and marginicollis. 4. Fig. 1—-Elidiptera callosa Spin., right tegmen: fig. 2—Elidiptera (2?) woodworthi Van D., right tegmen. Text figures 1 and 2 illustrate the tegmina of &. callosa and E. woodworthi and show the difference between them. In the former Sc and R fork near the base and R is simple. M. forks about the apex of clavus, and there are five apical Ms. In the middle of the apical third of the tegmen there is a round callus which causes the apical third of the tegmen to curve, the upper surface convex and the lower concave. ‘This throws all the apical veins out of the straight, especially the Cu, and M,,,. The effect of this is to give the tegmen a twisted appearance indicated by its generic name. In E. woodworthi Van D. the tegmen and venation is of the normal Achilid type, the tegmina overlapping when at rest and the veins are but slightly curved or bent but not twisted. The fork of Sc and R is further from the base and R has three apical veins. * The first fork of M is well beyond the apex of clavus and has three apical veins. 3 In £. callosa there is one pronotal carina on the shoulder, in E. wood- worthi there are two. For these reasons | do not think that they can remain in the same genus. Some of the species at present under Elidiptera Spin. will fit into Angeleusa Kirk. and have a distinct median carina on the clypeus. Other Species, such as EH. woodworthi, have no median carina on clypeus and I am uncertain of their correct position. 62 THE CANADIAN ENTOMOLOGIST. NEW CICINDELAS OF THE FULGIDA GROUP. (COLEOP.). BY EDWIN E. CALDER, Longmeadow, R.I. Cicindela azurea, new species. General form of fulgida but somewhat larger and a little more elongate. Above deep bluish green with strong metallic lustre. Beneath bluish green; surface of the abdomen, legs and thighs very thickly clothed with white hairs; legs deep blue. Maculation; humeral lunule wider than in filgida, unbroken ‘at the shoulder, longer, almost reaching the middle band. The middle band uniform in width, reaching the margin, not dilated thereon and-only very slightly prolonged backward. The descending portion of the band longer and more drooping than in fulgida, closely approaching the apical lunule. — Length, 13mm. Width, 5 mm. This form resembles C. parowana as to color and general appearance but differs very markedly in the character of the middle band. Two specimens from Penticton, B.C., J. B. Wallis, August 13, 1909. Type in J. B. Wallis collection, Winnipeg, Man. : Cotype in EK. EF. Calder collection, Longmeadow, R. I. Cicindela fulgida elegans, new var. Form, size and general maculation similar to fulgida. | Above deep chestnut brown with distinct metallic purple lustre. - Beneath, lower part of the abdomen deep greenish black; upper part, extending from sternum to the head, copper bronze, more pronounced on the sides of the thorax. Markings very similar in character to C. parowana. The humeral lunule uniform in width, unbroken at the shoulder, less oblique than in fulgida, longer and more drooping extending almost to the middle band. The middle band shorter and less angular than in fulgida, extending to the margin, largely dilated thereon and prolonged backward but not to the marked degree as in parowana; the descend- ing portion of the band elongate and drooping, closely approaching, but not quite reaching the apical lunule. Length, 12 mm. Width, 5 mm. Westbourne, Man. J. B. Wallis, August 14. Type in E. E. Calder collection, Longmeadow, R. I. Cicindela fulgida subnitens, new var. Similar in size, form and maculation to fulgida. | Above, dull black, much less metallic than fulgida. Beneath wholly black, without any tendency to greenish. This form may possibly be only a color variety of fulgida but the decided departure from the type as noted in the black color of the under surface de- serves recognition. Lincoln, Nebr., F. N. Schoemacker. = fe mee re Sere ea! Pe - A a” bes ware ie, ea. ee, els tn he THE CANADIAN ENTOMOLOGIST. 63 NOTES ON NORTHERN BRITISH COLUMBIAN COLEOPTERA. BY “MES: W. W. HIPPISLEY, - Terrace, BG: Terrace is a small town situated on the Grand Trunk Pacific Railway in the fertile valleys known as Lakelse and Kitsumgalum, ninety-five miles east of the terminal at Prince Kupert and 500 miles northeast of Vancouver. The two valleys are separated by the Skeena River, that called Lakelse lying to the south and Kitsumgalum to the north; taken together they number some 200,000 acres, Lakelse being the larger of the two. The soil is varied, a stiff clay on the flats, sandy by the river and gravelly on two large plateaus. The district is heavily timbered with spruce, hemlock, cedar and cottonwood, some yellow pine and yellow birch, and a sprinkling of balsam fir; some of the older clearings are overgrown with poplar and birch saplings, alder, elder, and willow. Most of the insects collected during the past two years have been taken on or near our ranch “West Lodge,’ some three and one-half miles southwest of Terrace as the crow flies, or six miles by the road. Most of this material has been forwarded to Mr. C. A. Frost of Framingham, Mass., to whom I am indebted for the identification of the species mentioned in the following notes. It is hoped that they may prove to be of some slight interest and value, coming as they do from a country so far north and one almost entomologically unknown. Elaphrus riparius Linn. In two years collecting on the south side of the Skeena River, this handsome insect has only been taken in two places; the first time on the margin of a small pool on a flat some 50 yards distant from a spring ereek, where they were driven from cover by treading about on clumps of a fine sedge while searching for water beetles, about the first week in June, 1920. Ten days or so later they were found in some numbers on a part of the garden, - behind the house, that had been flooded throughout the spring by the water from a small swamp. ‘This stagnent water supported a thick growth of algae and when the water failed this algae with myriads of tadpoles formed an evil- smelling scum that dried in flakes, beneath which were found the Elaphrus. Both garden and pool were in the full glare of the sun. From comparison with the types in the LeConte collection, I am informed that many specimens of this series agree with punctatissimus Lec. while others are more like similis Lec. in shape. Among these taken near the garden were a few that were of a red-bronze tint, instead of the usual green; these specimens are also slimmer with narrower thorax and of a shining brassy color beneath, less green on the femora, metasternum smooth and shining, ventral segments less hairy, punctation beneath less deeply impressed and more scattered, especially toward the apex. As this insect somewhat resembles pallipes Horn, it may be the form described from B.C. as purpurans by J. F. Hausen (Can. Record of Sci. IV, 1891, p. 251) and listed as a variety of pallipes, but the Terrace specimens do not have the legs paler than in riparius, while the elytral apices are not narrowed, nor is the punctation of the propleura and sides of abdomen as sparse as in pallipes. Elaphrus clairvillei Kirby. Two specimens of this species were taken \ 64 THE CANADIAN ENTOMOLOGIST. about the same time, and they are identical with the eastern specimens of this species. Elaphrus clairvillei frosti new var. This very pretty insect differs from Kirby’s clairvillei in its narrower thorax with median and sub-apical impressions more deeply indented, and with the discal elevations more sparsely and finely punctate, while the under surface is less coarsely punctate and the side sutures less sinuate; the front of the head is narrower and the eyes proportionately larger; elytra not so shining, with the punctation very fine, scattered, and not in wide rows between the discal foveae as in clairvillei; the color of the entire upper surface is deep, rather dull, olivaceous green (almost exactly as in olivaceus Lec.) with smaller purplish foveae ; under surface a lighter shade of green; tibiae and femora colored much as in clairvillei, with the tarsal joints slightly darker. The specimen at hand measures 8 mm. while a specimen of clairvillei is slightly over 9 mm., and is of a much more robust form. This strikingly distinct form, which seems almost to merit a higher standing than a mere variety, is dedicated to Mr. C. A. Frost in recognition of his great assistance to the writer. The type is in his collection. Pterostichus herculaneus Mann. This species is one of the first beetles found in the spring, when it is present in small numbers, perhaps two or three at a time, beneath the loose bark of cottonwood logs and stumps, and under the bark of partially decayed hemlock and yellow birch. In autumn their habits are slightly different, as they then seek shelter for the winter in powdery dry stumps, dry rotten logs (hemlock or poplar preferred), at the bases of moss- covered cottonwood stumps, or under a sunken mossy log. They occur at times with /phthimus opacus in decaying logs or beneath loose bark. | The species is not very plentiful and one could perhaps take a dozen in a day by diligent search. Hydrobius scabrosus Horn. A few specimens of this beetle were taken in May, 1920, from beneath moss growing at the edges of a rapidly -flowing creek. The temperature of the water is about 45 degrees Fahr. both in summer and winter. The moss is partially submerged and grows on sunken logs, branches and twigs that have fallen into the water. The beetles are not seen until the moss is pulled off and laid on the bank upside down, when they com- mence to crawl about. On March 29, 1921 (since writing the above note) while there was still two feet of snow on the ground, four more specimens were taken from this moss after being gathered in the creek and carried to the house. Eros simplicipes Mann. About half a dozen of this pretty Lycid were taken on the wing, the last of May, 1920. The flight is weak and wavering, about six feet off the ground, and they are easily captured by hand. They often light on the dress or hand of the would-be captor as they dance about in sunny glades among the green timber on still warm days. The red of the elytra has a distinct orange tint quite noticeable when compared with examples of hamata or aurora. The quadrate impressions of the elytral intervals are very even, the costae fine; the tibiae and femora are red, the tarsi black as are the antennae, though the head and first joint of the antennae have a reddish tinge. Length ay g THE CANADIAN ENTOMOLOGIST. : 65 of malei2mm. My correspondent writes me that these specimens are identical _ ‘with those so named in the LeConte collection. Eros nigripes Scheffer. With the preceding species were taken five specimens having the legs, antennae, head and under parts black throughout; antennae broader and heavier; color of elytra deep scarlet, with the quadrate impressions of the intervals irregular and uneven in size, costae much coarser and the form broader than in simplicipes. Length 9 to 10 mm. There is one specimen of this species in the LeConte collection at Cambridge, Mass., without ) name. A specimen of this has recently been sent to Mr. Charles Scheffer of the Brooklyn Museum who states that he cannot see that it differs from his nigripes which was described from Minn. (Jour. N.Y. Ent. Soc. Vol. XIX, IQII.) except in the slightly weaker thoracic costae. : Eros hamata Mann. Four specimens of this handsome species were taken in 1920, usually while resting on the trunk of a green spruce. The quadrate impressions in this species are thickly covered with short appressed hairs of the same color as the elytra and thorax; the legs are red and the tarsi piceous; the head, first antennal joint and metasternum dull red; ventral seg- ments black except the last which is brownish yellow. Length 15 mm. The specimens correspond with those named as above in the LeConte collection. Lucidota (Ellyschnia) corrusca Linn. ‘This is extremely common here all the season, being one of the first insects to appear after the snow melts, and one of the last to go in the autumn. It is very partial to the flowers of the pearly everlasting. Silis spinigera variety munita Lec. One specimen was taken in June, 1920, on the flowers of the red osier willow or dogwood. Silis pallida Mann. ‘Three specimens taken; two flying about fire-weed blossoms and one resting on a thimbleberry leaf, June to July, 1920. Calopus angustus Lec. Seven specimens of this rare Oedemerid were taken in the early part of the spring of 1920, five being taken before all the snow had melted. These were all found beneath the loosened bark on decaying pine stumps from which they seemed to have recently emerged as fresh holes were noticed in each case close to the sweil of the roots. A week or so later one was found drowned in a tub of rain water by the door early in the morning. It seems probable that its early appearance in spring together with the indica- tions that it flies at night, may account for its rarity in collections. | The seventh specimen was taken from the water tank of a gasoline engine. Omosita discoidea Fab. Two fragments of the knuckle-end of a beef shank yielded upwards of one hundred of these little insects during a space of about three weeks at the end of May and beginning of June, 1920. They crawl into the fine bony net-work and can scarcely be seen until breathed upon. When the bone is sharpely tapped on a board or table they fall out. Only bones having this net-work of fibre seem to attract them. In this species the yellow markings of the elytra are sub-basal to median instead of apical as in O. colon. Discoidea also has scattered flecks of yellow toward the elytral apices. 66 ; THE CANADIAN ENTOMOLOGIST. Leptura aspera parkeri new var. Form longer and slimmer, elytra reddish-testaceous (of a shade similar to that of some of the redder forms of Brachyleptura rubrica Say) with the — punctation much finer and the asperities not so pronounced, tips rounded and margined; the head is more sulcate with finer punctation, with the first four joints of the antennae more shining, not so coarsely punctate or hairy as in the black form, fourth joint two-thirds the length of the third and the two together — but slightly longer than the fifth. Two of the abdominal segments have the apical margins glabrous with a cross band of yellow-brown, last segment brown with a fringe of yellow hairs. Length 14 mm. Width 3 mm. This form has been given the varietal name parkeri in honor of the author’s father whose keen interest in the insect fauna of this region has been — a great encouragement to the writer. The type has been placed in the — collection of Mr. C. A. Frost of Framingham, Mass. A FURTHER NOTE ON THE GENUS PLATYPREPIA (LEPIDOPTERA) BY J. MCDUNNOUGH, Entomological Branch, Ottawa. It had been my intention to consider the matter of the family position of the genus Platyprepia closed with the publication of Dr. Dyar’s reply (Can. Ent. LIV, 20) to my previous statements (Can. Ent. LIII, 167). Unfortunately however an ‘Author’s note,’ inserted by Dr. Dyar in the page proofs of his article and set up by the printer without consultation of the editor, calls for a reply as the statement contained therein is erroneous. Dr. Dyar claims in this note that, whereas in Platyprepia veins 7 and 8 of secondaries are separated at the base, in Arctia they are united, and he would use this apparently as a character to differentiate the two families Arctiidae and Hypsidae. It might be pointed out in passing that if this character should be used, then A pantesis and numerous other Arctiid genera would fall into the latter family. However, as a matter of fact, vein 7 in Arctia does not coalesce with 8 to the extreme base of the wing; it branches off from 8 about 2 mm. from the base in exactly the same manner as is found in Platyprepia; in both genera it is much reduced in size as compared with 8, which is greatly swollen at the base, and this reduction of size has been carried almost to obsolescence in some specimens of Arctia caia; an €xamination of a series of this species, especially large females, clearly shows however the basal separation of the two veins and I have specimens before me as well marked in this respect as any of Platyprepia guttata. While I have no objection to the transference of Platyprepia to the Hypsidae if sufficient proof of the soundness of this transfer can be given, I do claim that up to the present neither Sir Geo. Hampson nor Dr. Dyar has given us satisfactory reasons for making such a change. THE CANADIAN ENTOMOLOGIST 67 NEW SPECIES OF THE SYRPHID GENUS CHILOSIA FROM CANADA (DIPTERA) BY C. HOWARD CURRAN, Orillia, Ontario. (Continued from Page 20) Chilosia orilliaensis, new species. Eyes pilose; arista black, bare; thorax deep blackish green, its dorsum cupreous bronze; abdomen shining blackish green, first two segments chiefly opaque ; wings clouded or infuscated with dark luteous; scutellum with bristles which are scarcely distinguishable in the male owing to long pile; third antennal joint small, reddish, black above; abdomen of female almost wholly shining. Male. Length 8 to 10 mm. Face and front shining greenish black, thinly covered, except the tubercle, an area on its lateral slopes and the cheeks, with fine whitish pubescence which is condensed as a band below the antennae ; ‘side margins with whitish pile, face elsewhere without pile; in profile very slightly concave or almost straight to the tip of the large, rather prominent nose shaped tubercle, thence shortly concave to the oral margin, which is convex, not quite as prominent as the antennal base and much less prominent than the tubercle. Frontal triangle a little prominent, in the middle with a more or less distinct brassy tinge; in the middle with a rather broad longitudinal depression which is narrower above; margins very narrowly white pollinose; pile of frontal triangle rather stout, long, black. Antennae luteous or brownish luteous, first joint always darker, third joint about equal in length to the first two, small, little longer than broad, its lower end usually more sharply rounded. Arista long, slender, bare, black, the sub-basal quarter a little swollen. Vertical triangle dull black, black pilose in front,-yellow behind, sometimes nearly all black or with chiefly yellow pile. Eyes brown or yellowish brown pilose on the upper half with yellowish or grayish yellow pile below. Posterior orbits narrowly white pollinose on lower two-thirds, with opaque black pollen on the upper half except against the eyes at the upper three-quarter area; the pile is white on the lower half, more brown or blackish above and the hairs ovrhanging the eyes are black. Thorax and scutellum shining blackish green, the dorsum, except the sides, with a cupreous bronze reflection. Pile variable, but usually chiefly black on the dorsum, intermixed with some yellow or fulvous hairs on the disc, some- times almost wholly black pilose, but often the pile is chiefly yellowish or ful- vous with the borders black pilose; there is always black pile at the humeri, base of the wings and on the postalar calli; pile on the upper half of the pleura almost always wholly black, but sometimes a few pale hairs intermixed, the lower half always whitish pilose. Scutellum usually with almost all long black pile, with a few paler hairs at the base but these sometimes wanting, at other times chiefly yellow pilose with black pile apically. In these latter speci- mens the scutellar bristles are usually quite distinct. The other bristles on the thorax are not conspicuous in the males. First abdominal segment more or less brownish, scarcely or moderately shining, the angles below the scutellum reddish brown, and often the anterior margin more or less yellow pollinose ; if shining, with a greenish reflection. Sec- 68 i THE CANADIAN ENTOMOLOGIST ond segment opaque black, the anterior margin very narrowly shining, the side margins, more broadly in front, shining greenish; third segment opaque, the apex very narrowly shining, and apparently inclined to be reddish in some speci- — inens, lateral margins shining greenish, expanded in front to occupy about one- — third the width of the segment on each side, but the shining area indistinctly defined. Fourth segment wholly shining, and usually with a metallic bluish reflection, but sometimes metallic blackish green. Hypopygium shining black- ish green, finely, sparsely whitish pubescent and with mixed yellowish and black pile. Pile of the abdomen moderately long, on the basal angles long pale yellow- ish, yellow or fulvous, the sides of the abdomen with similar colored pile to that on the basal corners, except the apical quarter to half of each segment, the light colored pile extending as triangles on the basal corners of each segment; pile elsewhere black or brown. Legs shining greenish black ;'tips of the femora, anterior four tibiae except a broad band mostly beyond the middle, yellow; apex of hind tibiae and first two joints of middle tarsi reddish, brownish yellow or brown; anterior tarsi brown basally in most specimens. Wings strongly tinged with brownish or brownish yellow, more so anteriorly; veins brown; stigma yellow. Squamae yel- low, tinged with brown, with brown margin and brown fringe. Halteres luteous, the tip of the knob brown. . Female. Antennae reddish, basal joint usually brownish, third joint larger than in male, brownish above and apically its end truncately rounded but frequently more pointed below. Face moderately concave between the antennal base and the small but prominent tubercle, only slightly concave below the tu- bercle. Front shining black, with a brassy reflection in the middle; a shallow longitudinal median groove usually indistinct just after its inception a little above the antennae, running to the ocellar triangle; lower quarter of front silvery white pollinose contiguous to the eyes, above which the sides of the front are black. Pile of the front usually nearly all yellowish with black pile across the ocelli, some black hairs intermixed above the antennae, the -vertex with yellowish pile. Posterior orbits thinly grayish pollinose above, white below. Thorax and scutellum shining blackish green, the dorsum with a~more or less distinct brassy or bronze reflection. The pile of the dorsum is short reddish yellow, on the pleura long, white; postalar callosities with two black bristles, two to four short ones above the base of the wings, and rarely a long slender one on the posterior part of the mesopleura ; scutellum with short white or pale yellow pile and from four (usually six) to eight long slender black bristles on the apical margin. ; Abdomen shining blackish green or blackish; first segment-with the corners — below the scutellum reddish luteous ; second segment with an obscure opaque area on the anterior three-fourths occupying about one quarter the width of the segment, or less, on each side of the middle and often interrupted longitudinally by a shining median line; third segment with a similar but smaller subopaque — marking, but sometimes there is scarcely a trace. Pile on the abdomen yellow, — 4 + ee tial arte 10a pg he a ae | han enti ti on the base and the lateral segmental triangles usually whitish; the antero-lat- eral more smooth triangles are limited by a condensation of subappressed yel- lowish pile; on the apical half of the disc of the third and fourth segments _ the pile chiefly appressed black, but the yellow hairs which are intermixed are most prominent, \ THE CANADIAN ENTOMOLOGIST 69 Legs as in the male but the bands on the anterior four tibiae are narrower and brownish, the basal three joints of the anterior four tarsi are reddish. Squamae white, with white fringe. MHalteres yellow. Wings as in the male, but frequently more clouded beyond the middle anteriorly. Holotype, 8, Orillia, May 8, 1921. Allotype, @, Orillia, May 22, 1921, collected by the author, in the Canadian National Collection, Ottawa. The descriptions are drawn from 57¢ and 8192 specimens, taken at Orillia between May 5th and June 18th, 1920 and 1921 and one male, Ottawa, Ont., May 22, 1921 (J. McDunnough). The species shows considerable variation in the color of pile, antennae and legs, and also the facial tubercle is more or less variable. Occasional females have the oral margin more prominent than described, but this varies and inter- mediate specimens occur. The shape of the third joint of the antennae varies especially in the females. In many specimens the end of the third joint is more produced below, while in others it is rounded rectangular and narrower, being not twice the width of the second joint at its broadest. This species is very close to hoodiensis Bigot, but is at once distinguished by the lighter pile of the face and the paler pile generally. In hoodiensis the _ thorax is black pilose. From borealis Coq. it is distinguished by the lighter an- tennae, bare arista and opaque abdomen. From occidentalis and petulca by the _ paler antennae, darker pile on thorax and abdomen as a rule and abscence of hairs on facial slopes. In Hunter’s key (Can. Ent., vol xxviii, p. 229) the fe- male traces out to laevis Bigot but is readily distinguished by its larger size, etc. A very abundant fly on Cowslips, fairly abundant on Wild Cherry in the vicinity of deep woods and on flowers of Osmorrhiza claytoni in sub-swampy woods. The most common species of the genus in Ontario. Other species are frequently taken in company with it. Males are most abundant towards evening. Chilosia columbiae, new species. Antennae small, arista bare, black; eyes yellow pilose; thorax wholly light yellow pilose; second and third abdominal segments more or less opaque; legs black, only the knees obscurely reddish. Male. Length 11 mm. Face shining black, thinly covered, except the tubercle, with yellow pollen which forms a broad band across below the antennae and extends narrowly down along the eye margins to the cheeks; side margins short yellowish pilose. Front not prominent; a deep sulca rising just above the polished antennal arch and reaching quite to the juncture of the eyes; in color metallic blue, with wholly yellow pile; front densely punctulate in vicinity of sulea, the sides obscurely golden yellow pollinose. Antennae brown, shining; _ third joint about twice as broad as second, a little longer than broad, its end rounded, in color opaque yellowish red, its upper and apical border brown, dusted with whitish. Arista black, bare, longer than antennae, slender, the basal quarter a little thickened. Vertical triangle shining greenish black its pile yellow, but most of the hairs blackish on the anterior half. Posterior orbits yellow pollinose and with yellow pile, including the occipital ciliae. Eyes moder- ately densely yellowish cinereous pilose, whitish below. \s 7O THE CANADIAN ENTOMOLOGIST Thorax and scutellum shining blackish green, the dorsum with a strong brassy reflection, pile luteous yellow, not long but rather dense; pleura and ~ scutellum with similar pile, no trace of bristles. Abdomen metallic blackish green, slightly brassy; first segment moderately — shining, the corners under the scutellum brown; second segment opaque black, ’ except the very narrow posterior margin and the sides broadly, the opaque area cut off nearly squarely at the sides; third segment with a rather broad abbreviated — cpaque band near the hind margin in the middle, but with a very slender shining median stripe interrupting the opaque longitudinally; the opaque outline is vague; anteriorly and contiguous to the opaque markings and extending across © the anterior margin there is a metallic deep blue reflection. Pile on opaque - areas short, black, elsewhere longer, yellowish. =a Legs black, the knees obscurely reddish. Pile of the i= similar to that of thorax; decidedly short reddish beneath the femora and tibiae apically and beneath the tarsi; a patch of golden pubescence at the bases of. the anterior four femora. Wings distinctly fuscous, more marked basally and anteriorly, almost hyaline posteriorly ; veins brown; the tip of the fourth vein joins the third longitudinal at almost a right angle. Stigma yellow. Squamae pallidly yellow with yellow border and pale yellow fringe. Halteres brownish luteous, the knob ~ brown. . Holotype, 8, Cranbrook, B.C., May 8, 1920, (C. B. D. Garrett), in the writer’s collection. ~+ This species is very like C. lasiophthalma but the pile is lighter, the face is less produced downwards, and the abdomen is more elongate. It must closely resemble the male of punctulata, but the thorax is not densely punctulate, the arista is wholly black and the thorax is very shining. It must also be very — similar to sororia from Mexico, but the brassy thorax will distinguish it from” that species. It differs from petulca in the abscence of bristles on the scutellum. — Chilosia rita, new species. Arista bare; eyes bare; thorax and scutellum yellow pilose, the latter with black bristles; wings with yellowish brown cloud. Male. Length 10 mm. Face and front shining blue black, a grayish pol- linose band below the antennal prominence; side margins with short whitish pile; tubercle large, Roman nose shaped; face sub-triangularly concave from tip of antennal prominence to tip of the tubercle but the lower half of the con- cavity formed is convex; below the tubercle perpendicular to the oral margin, the anterior tip of which is on a plane with the posterior oral cavity. Frontal triangle with strong metallic blue reflection, with a broad sulea rising at the antennal arch and reaching the eyes at their juncture, the pile moderately long, black, not longest above. Antennae brownish red, first joint black, third joint as long as the first two together, oval, a little flattened above; arista Iong, slender, a little thickened near the base. Posterior orbits grayish yellow pollinose below, opaque black above, below with sparse whitish pile, above with black, but at — the vertex with short yellow pile, the orbital ciliae black. Vertical triangle black pilose, the hairs at the back yellowish basally. Eyes contiguous for long distance, the vertical triangle small and narrow. Thorax and scutellum shining blackish green, the dorsum with a brassy ~ Bhs G3 THE CANADIAN ENTOMOLOGIST 71 lustre, the pile luteous, on the sides of the dorsum and on the mesopletra black, moderate in length, longer on the scutellum which bears apical slender : black bristles. Abdomen shining greenish with a brassy reflection; first segment with about six transverse impressions; second segment opaque, the side margins, ex- panding in the middle and extending obscurely (subopaque) entirely across, shining ; third segment similar, but the middle of the segment less opaque and the shining band less broadly subopaquely interrupted. Pile of the abdomen reddish yellow, paler on the sides. Hypopygium with some black hairs intermixed. Legs black; tips of the femora and all the tibiae reddish yellow, the latter with a rather broad blackish band, tarsi yellow, the last joint and hind basitarsi except the tip, brownish. Legs with long pale yellow pile, the anterior four femora with black pile apically and fulvous pile antero-ventrally, hind femora with short bristle-like black pile beneath. Wings clouded with luteous, veins mostly piceous, but brown postero- apically; stigma yellow. Base of 2-3 longitudinal vein with about 12 short, fine bristles. Squamae whitish yellow, fringed with luteous and with luteous fringe of pile. Halteres yellow, the knob darker. Holotype, é, Orillia, Ontario, May 5, 1921, (C. H. Curran) in the auth- or’s collection. Differs from the aoe of the fristis group in having bare arista, and in addition may be distinguished from the species in that group as follows: from pallipes in having no pale markings on thorax ; from tristis, similis and leucoparea in its more extensively yellow legs, etc; from skinneri in its larger size and largely black legs. Chilosia rita, new species. Antennae luteous, arista brown, bare; face with fine pile on slopes; front as long as face, not sulcate. Length, 7.5 to 8 mm. al. 7.5 mm. @ Face and front shining black, the sides of the face and across below the antennae silvery pollinose, extending _ very narrowly up the sides of the front on the lower fifth; face considerably concave between antennae and prominent tubercle, and thence perpendicular to the oral margin which is only slightly below the eyes at its anterior point; face with very fine whitish pile on lower central slopes and short silvery pile on side margins; front with short whitish pile below, with longer black or brown pile on upper two-thirds and immediately above the antennae and a few scattered black hairs among the pale ones; posterior orbits white pilose below and with whitish gray pollen, black opaque above with black pile. Eyes bare antennae reddish yellow or luteous, the basal joints infuscated, third joint a little darker dorsoapically. Thorax, scutellum and abdomen blackish blue, wholly shining; thorax chiefly short black pilose, but when viewed from in front appearing whitish ; there is a triangular area of yellowish pile on the front of the dorsum, the pleura entirely whitish pilose. Scutellum with brownish yellow or brownish pile, appearing pale in most lights, its margin with three or four pairs of black bristles, and some stout black hairs laterally; postalar calli and the sides of the dorsum before and behind the suture with two to four black bristles, and 72 : THE CANADIAN ENTOMOLOGIST _ - one to three bristles on the mesopleura. Abdomen wholly sparsely whitish — pilose, pile a little longer basally, sub-appressed except on the anterior angles “i of the second, third and fourth segments. Femora black, their tips luteous; front coxae obscurely luteous, as well as a spot on’ the thorax above them extending to the partly obscurely luteous humeri. Anterior four tibiae luteous : or yellowish with broad, ill-defined median blackish bands, hind tibiae paler — at ends only; tarsi obscurely luteous, the apical joints darker; hind tarsi more- brownish. Wings almost hyaline, stigma pallidly yellowish; veins brown, yellow at base of wing; first posterior cell acute, last section of fourth vein a little bent at its basal fifth: ‘There are five minute bristles on R,.,; before the furcation: Be. Squamae white, with whitish fringe; halteres yellow. . Holotype, ¢, Macdiarmid, Ont., June 7, 1921, (N. K. Bigelow), in the Ontario Museum, Toronto. Paratypes, 9, same data, in the Ontario Museum; ?, same data, in the writer’s collection. ~ This species is distinct from any so far described from North America in having the eyes bare and the facial slopes pilose. It belongs to a distinct group, although its general structure places it close to the tristis group. AN APPEAL FOR AID. The following letter which has been received by the Secretary of the [Entomological Society of Ontario speaks for itself. : Dear Strs:—The ‘Mikrographische Gesellschaft” has been in existence in Vienna for ten years and has at present about 50 members. Its object is to popularize microscopy or rather those branches of the natural sciences which rely upon the study of the universe in the smallest space. At the same time it extends and affords opportunities to non-members to whom the use of our laboratory, consisting of five rooms, is offered gratuitously. Through the extreme decline in the value of Austrian currency its finances have come into a most critical state. Before the war the society was able to cover its expenses and the upkeep of the laboratory out of its modest income. But our means are now exhausted and we are unable to procure even the most urgent expedients, such as instruments, reagents, colours, glass articles, photographic supplies, etc.. the prices of which have arisen enormously, not to mention the — increased cost for gas and electric current. Without prompt assistance the society will soon be obliged to dissolve and to deprive the intellectual people of our unhappy city of a place of scientific study and research. The unfortunate, poorly nourished intellectual classes of Vienna are facing — a winter of hardship and privation which acts as a spur to seek education and — enlightenment with a view of paving the way for a better future for themselves, and, let us hope. for the benefit of all mankind. We therefore beg leave to appeal to you, Gentlemen, who are pursuing similar noble objects, to make it possible for us, through an accommodation in your own sound money, that our society may be saved and continue with its work. Please accept our heartiest thanks in advance. We are, Gentlemen, gratefully and sincerely yours, MIKROGRAPHISCHE GESELLSCHAFT WITEN, Treasurer; Paul Frenzel, Vienna vi, Theobaldgasse ii. Mailed May 26th, 1922 «Che Canadian Entomologist ' Vou. LIV. ORILLIA, APRIL, 1922. No. 4. POPULAR AND PRACTICAL ENTOMOLOGY METHOD OF PROCEDURE IN INSECT LIFE History INVESTIGATIONS. BY WM. P. HAYES, Assistant Pntemologi:t, Kansas Agriculturat Experiment Station*, It is hardly necessary to emphasize the importance of life history investigations as an aid to the control of injurious insects. To the economic entomologist is allotted the development of methods of suppression, and without some knowledge of the life history of the insect in question, his efforts to control may be futile. It is, therefore, clearly obvious that the first effort in attacking the problem of insect control must be the acquisition of an understanding of the imsect’s life history. The writer as a novice in entomology, about seven years ago, was assigned to Southern Kansas and placed in charge of a field laboratory established for the purpose of working out the life histories of two serious insect pests of that part of the state. At the time a prepared schedule was furnished for the methodic study of insect life histories. Since then the value of such a schedule has been more fully realized. Investigators are far too frequently found who do not realize how much they know about a given subject or animal until they have subjected themselves to the processes of orderly arrangement. when the results obtained are found to be surprising and satisfactory. Often there has been no attempt to classify data which are obtained by a poor method of approach. Their knowledge is merely a mass of scrambled observations, which, if untangled, may lead to many unconsidered possibilities, and in recording their facts they are apt to omit many important matters which are overlooked in a forest of tangled ideas. They do justice neither to themselves nor their readers. They may have many times the number of facts which they record and the reason they are not recorded is the lack of systematic arrangement. Far too many life history papers exhibit this defect. | Undoubtedly a partial solution of, or at least an improvement in the character of life history investiga- tions, lies in the possession and use of an orderly plan, as is here suggested. The first and most important starting point is an accurate determination, by a specialist, if necessary, of the species under consideration. Its correct scientific and all common names should be known, and a complete bibliography should be made up. Special literature should be secured and copies of state and national laws affecting entomology should be available, especially those pertaining to quarantine regulations if the species may in any way be involved in legal entanglements. After the bibliography has been prepared, the investigator has learned *Contribution No. 73 from the Entomological Laboratory of the Kansas Agricultural Experiment Station. aeiet a ea 74 THE CANADIAN ENTOMOLOGIST. ‘ x what is-khown ‘about the insect. Adequate laboratory facilities should then be available and a system of record keeping established. This should include besides observations on the animal, statistical, climatological, geological, and | R miscellaneous data that may have a bearing on the species in question. The first steps in such a study will depend to a large extent on the time of year in which the work is begun and the corresponding stage of the insect’s development. ‘hat is, if work is begun in the spring and the insect is in the adult stage, the first observations will be on the mature form. However, a logical treatment should begin with the egg and the study develop as the insect proceeds through its various stages of metamorphosis. In the egg stage there are at least four important points to be noted; first, an adequate description of the egg which will permit of it being recognized by others; second, the embryology or development of the egg. This point is important and a great amount of data can be amassed on the one subject. Nelson’s “Embryology of the Honey Bee” is an example of the vast amount of material that can be assembled on the development of an insect egg. The third point is the duration of the egg stage which should be known under different climatological conditions — which affect the length of time required for development. Large series should be studied in order to obtain averages with a minimal probable error. Lastly, the method of hatching should be carefully investigated. This 1s often a weak and critical stage in the insect’s life and important control measures might suggest themselves at this time. More will be said concerning oviposition habits of the adult insect. The next stage is either the larval or nymphal, depending on the kind of metamorphosis, and here a good description is desired and the anatomy both external and internal should be worked out. The rate of growth and number of moults are important. It is surprising how little is known of the method of moulting and the frequency of its occurrence in many of our common species. The process of moulting may be variable and the food supply may have a decided influence on the time of moulting. “The size of the insect in each instar may have an important significance. Davis, of Indiana, is now working on the size of the various instars of white grubs and can identify species by their size, and Dyar has devised a system of proportions whereby the various sizes of caterpillars can be computed if the size of one instar is known. The duration of the complete stage varies and in many larvae a prepupal condition is assumed. This again is a critical stage where effective control measures may be applicable if the species is destructive. Before pupation, pupal cells are often con- structed, a knowledge of the method and the locality where they are built being desirable. Habits of feeding and methods of securing protection are important, and the character and degree of injury are vital points. The rearing of large numbers over a series of years. is desired to obtain the foregoing points under various conditions. The pupal notes likewise involve a description that is complete and a knowledge of the anatomy is necessary. Important post-embryonic changes are occurring within the pupa and much work has been done on this subject which is known as histogenesis. ‘The length of the pupal stage varies from a HE CANADIAN ENTOMOLOGIST. 75 few days to many months, or even years. ‘The Hessian fly has recently been -noted-as living over four years in the papurium, which fact has an important _ influence on the control of the species: The transformation from the pupa to the imago is an important phase in the insect’s life economy. | Now the adult must be considered. Again a description should be given and thorough morphological and physiological studies made. The period from transformation to complete maturity differs in some forms. In ants there is an _ interpolated stage known as the callow, and in May flies a sub-imago stage. _ Color changes and other points can here be noted. The size of the insect may _ have a relation to the amount of food supply and this in turn may influence the duration of adult life. Weights and especially dimensions are useful in making taxonomic determinations. An average length of life should be computed under both natural and artificial conditions. Various foods may influence the - duration and tests can be made with food and without water, also without food and with water. a Ability to distinguish the sexes is necessary and with some species this is hard to do superficially. The secondary sexual characters are used in this connection, and when lacking one must resort to the primary characters. The x relation of size and color to sex is a point to note and the proportion of sexes has an important bearing. In Lachnosterna, the males predominate at lights 3 during the spring flight, while a larger number of females are found on the food plants. With different insects, the proportion may vary at different seasons, so they should be observed for these data in the spring, summer, and fall, as well as during hibernation. Likewise, the sexes may vary during flights and under the influence of temperature conditions. SS The number of generations may vary in a season, and the maximum, minimum, and average number of broods are important considerations. These again are determined by environmental conditions. The duration of the com- plete life cycle with its minimum, maximum, and average broods-can then be summed up. With a tentative knowledge of the life cycle now at hand, the _ investigator is in a position to make a more thorough study of the life economy _ of the insect which involves consideration of the ecological features. . To » enumerate these would require too much time. However, a few of the following _- points should not go amiss. Habits of the species are ecologically important _and require a knowledge of food plants, of what part, such as leaf, fruit, bud _ or root, is attacked, the susceptibility of different varieties of food plants, tests _ with other food plants and the occurrence on other than food plants; or, if _ either nocturnal or diurnal feeding periods. Cannibalism as practised by some e insects has a bearing on the method of rearing some species which must be kept _ separate in laboratory cages. The same is true of those with predaceous habits in either the larval or adult stage. The food plant investigations may suggest trap crops or other measures of control, such as clean culture. oe Reproduction in insects is tremendous at times, and a knowledge of the processes of fertilization, polygamy, polyandry, and parthenogenesis are highly 76 THE CANADIAN ENTOMOLOGIST. important. The places of oviposition, the formation of the egg cavity, time required to deposit the egg, number of eggs deposited, dependence of oviposition on food supply, and the effect of oviposition on the plant, require careful observations and well-kept notes. These activities should be observed in the laboratory and field and differences noted. Other factors involved and perhaps influenced by the environment are the periods of first, last and maximum ovi- position, as well as the rate or number of eggs laid daily. Protection by mimicry is an ecological factor about which much can be written. Other methods of protection are found at all stages of various insects. The eggs may be protected by being deposited internally, by isolation, external structure, or protective secretions; larve and adults by places in which they develop, by external structures, such as spines, repellent odors, protective con- structions (caddis flies) and protective excretions. | Habit sometimes offers protection, and we find strong fliers, swift runners and active swimmers. — Color- ation involves mimicry and warning coloration, both of which. afford protection. The pupa, to shield itself, may hide, construct cocoons and earthen cells, roll leaves, form galls, or be protectively colored. All these are important in life history investigations. ) Theoretically, the annual progeny of a single pair should be computed and the number of individuals per acre should be estimated on a basis of field counts. The rate of multiplication is directly influenced by the available food supply which places restrictions on the numbers present. Seasonal history is important and such factors as hibernation and zstiva- tion must be considered. The time of entrance into hibernation is affected by temperature which in some species determines whether entrance shall be gradual or sudden. Different species have different stages passing the winter. The individuals may be congregated or found singly and this may be a factor affecting mortality at the time of entering hibernation. There is also mortality during and at the time of emergence from hibernation. The time of emergence from hibernation, like the period of entrance, is influenced by climate conditions and - it may be abrupt or gradual. Sometimes re-hibernation occurs. The number and percentages of individuals entering and surviving hibernation ought to be observed. The finding of food in the spring is an important problem for the individual and one can determine the nature of the first food supply, the pre- ferred food, how far they will go for it, and the duration of life of hibernating individuals. All these factors influence the relative abundance of the species and the amount of damage they are capable of doing in the spring. The abundance of pests that did so much damage in Kansas during the spring of 1921 can be traced to the mildness of the preceding winter which caused little mortality in hibernation. The progress of infestation during the season should be followed and such points as the time and effect of the maximum infestation and percentage of the crop destroyed should be noted. | Nothing has so far been said of para- sites, predaceous enemies, and fungous diseases. These should all be studied. Corr a ee ee ee ee ee nei THE CANADIAN ENTOMOLOGIST 77 The following list will serve to show the number of points of attack that may be studied to work out control measures; under natural control we have cannibalism, adverse climatic conditions, fungous and bacterial diseases, -para- sites, and predatory enemies; and, under artificial control, traps (trap crops, lights, shelters, and trap rows), insecticides, repellents, certain types of farm machinery, restriction of spreading by quarantine, disinfection and fumigation, and cultural methods of control. Another desired feature is experimental farm work involving a sufficient knowledge of farming methods to conduct time of planting tests, variety, fertilization, cultivation, soil and isolation tests as applied to insect control. Obviously, the investigator should have a broad fundamental training and his time and available funds should be guarded against wasted energy. A PARTHENOGENETIC MAYFLY (AMELETUS LUDENS NEEDHAM). BY WILBERT A. CLEMENS, Department of Biology, University of Toronto. The female subimago and nymph of Ameletus ludens was described by Needham (1905) from material taken at Newport, N.Y. The nymph of this -mayfly is a small brook-inhabiting form which occurs very abundantly in the many small brooks in the vicinity of Ithaca, N.Y. At the season of emergence the female subimagoes and imagoes are not uncommon along the banks of these brooks. A suggestion that reproduction in Ameletus ludens might be a case of parthenogenesis was made by Morgan (1911) who recorded unsuccessful efforts to find the male of the species in spite of extended and diligent search. In order to test out this suggestion the writer had this species under more or less constant observation from June 14, 1913, to July 30, 1915. From June 14 to June 30, 1913, only a few mature nymphs were found in the brooks and no adults were observed. Apparently the period of emergence was practically over since in early July no nymphs could be located. By. the middle of August the brooks had ceased to flow, there being only an occasional stagnant pool or some slight dampness and stretches where no trace of moisture was evident. On April 18, 1914, almost mature nymphs were abundant and on April 27 a male subimago was discovered resting on the surface of the water having just emerged. A short distance away a female subimago was also located. These were both taken to the laboratory and placed in wire cages but unfortunately the male failed to transform. No other male has been found although much time has been spent along the streams in search, hundreds of nymphs have been examined and many subimagoes reared. Females were fairly abundant during this year up to the middle of June and mature nymphs could be found up to about June 30 as in the preceding year. Again the streams were practically dry during mid- summer. 78 ‘THE CANADIAN ENTOMOLOGIST. On May 6, and again on May 8, 1914, eggs were dissected from reared females, placed in water in petrie dishes and kept in the laboratory. The water in the dishes was changed usually every other day. Fertilization could not have occured by any chance since all the nymphs were examined before being placed in the rearing cages. (The sexes can be distinguished in mature mayfly — nymphs by the size of the eyes and by the rudimentary genitalia). All the sub- imagoes which emerged were females and these were transferred to wire cages. The adults used in this experiment were dissected about 24 hours after the sub- imaginal moult. On October 5 a newly hatched nymph was found in one of the petrie dishes and examination of the eggs showed moving embryos. Hatching continued for over a week. The period of incubation was thus almost exactly 5 months. No record of the temperature changes in the laboratory was kept during this time except that on September 1 and 2 the air temperature was 28.3 C. and again on September 11 it was 15.5 C. Fertilized eggs of other species of mayflies were kept during this summer at the fish hatchery in Cascadilla gorge where the air temperature was con- ~ siderably lower and these hatched as follows: Hexagenia bilineata 29-40 days; Hexagenia recurvata 14 days; Ephemera varia 15 days; Heptagema tripunctata 11-23 days; Ecdyurus maculipennis 12 days. The long period of incubation in the case-of Ameletus ludens may be a characteristic which has made possible the existence of this species in brooks which are subject to mid-summer droughts. The presence of a_ thickened roughened coat on the egg would appear to support this belief. The egg is figured by Morgan (1913). : The seasonal history for 1915 was much the same as in the two previous years. Nymphs 4 to 7 mm. were abundant in January. Mature nymphs were present in large numbers toward the end of April. On April 27 many emerg- - ings took place and one female was observed ovipositing at 8.30 a.m. By June 7 only a few nymphs remained in the brooks and no adults were observed. These results show conclusively that Ameletus Iudens reproduces parthenogenetically. The finding of the single male indicates that the evolution toward complete parthenogenesis is not yet complete and that sexual reproduc- tion probably occurs in very rare instances. | Whether or not this partheno- genetic condition of Ameletus ludens is of local or general occurrence cannot be said at the present time. LITERATURE CITED. Needham, James J., 1905 Mayflies and Midges. N.Y. State Mus. Bull. 86, pp. 36-38. é Morgan, Anna H., 1911 Mayflies of Fall Creek. Ann. Ent. Soc. Amer. IV, pp. 117-118. . 1913 A Contribution to the Biology of Mayflies. Ann. Ent. Soc. Amer. VI, p. 371. THE CANADIAN ENTOMOLOGIST. 79 ANNOTATED LIST OF THE BUPRESTIDAE OF PENNSYLVANIA (COLEOPTERA). BY JOSEF N. KNULL, 3ureau of Plant Industry, Harrisburg, Pa. In the preparation of this list of Buprestidae, which is arranged according to Leng’s Catalogue*, a number of original rearing and collecting records and - observations have been utilized, to which have been added records from several private and museum collections, and likewise those in the Pennsylvania State Collection. | Various records in literature on this group, pertaining to Pennsyl- vania and adjacent states, have been included, since there is a strong possibility that several species recorded from nearby states occur here. The work was carried on under the direction of Prof. J. G. Sanders, Director of the Bureau of Plant Industry. The author is also indebted to Dr. Henry Skinner and E. T. Cresson Jr. for the privilege of studying the Horn Collection in the Academy of Natural Sciences of Philadelphia, and to the following persons for valuable records and suggestions: Messrs. H. E. Burke, A. B. Champlain, E. M. Craighead, C. A. Frost, H. B. Kirk, H. G. Klages, F. R. Mason, A. S$. Nicolay, H. B. Weiss and H. W. Wenzel. Polycesta Sol. P. angulosa Duv. (obtusa Lec.) Near Philadelphia (LeConte). A southern species which was probably imported in southern lumber. Recorded as breeding on Coccolobis laurifelia in Florida. Acmaeodera Esch. A. ornata Fab. Mount Holly, June 22 (V. A. E. Daecke); Carlisle Junction, April 27 (A. B. Champlain) ; Darby (H. W. Wenzel). A. pulchella Hbst. S: W. Penna. (Dr. Hamilton); Erie, July (H. G. - Klages). A. tubulus Fab. Common on flowers throughout the state in May and ‘June. Recorded as breeding in hickory and white oak (Quercus alba). A. B. Champlain reared an adult from dead redbud (Cercis canadensis) collected at Rockville. Ptosima. Sol. P. gibbicollis Say. Common where redbud (Cercis canadensis) occurs, in which tree the species breeds. The adults mature in the fall and pass the winter in their pupal cells. Chalcophora Sol. C. virginiensis Drury.- Common throughout the pine section of the state, breeding in partly decayed stumps and trunks of both hard and soft pines. C. fortis Lec. S. W. Penna. (Dr. Hamilton); Morris, June 20 (I. H. White) ; Endeavor, July 30 (Kirk and Knull) ; Charter Oak, June 18 (Author). Reared from dead white pine (Pinus strobus). Collected at Charter Oak. C. liberta Germ. A common species which breeds in dead pine. Chalcophorella Kerr. C. campestris Say. A common species which has been recorded as *Catalogue of the Coleoptera of North America, 1920, 80 THE CANADIAN ENTOMOLOGIST. breeding in dead sycamore (Platanus occidentalis), beech (Fagus americana), and willow (Salix nigra). The adults overwinter in their pupal cells. Dicerca Esch. . D. divaricata Say. A common species, which breeds in the heartwood | of a great variety of dead trees. D. caudata Lec. North East, Aug. 8, Charter Oak, June 5 (E. M.” Craighead) ; Harrisburg, Aug. 11 (H. B. Kirk); Cresco, June g (Author). — Recorded in the literature as breeding in birch (Betula nigra). . D. prolongata Lec. $. W. Penna. (Dr. Hamilton) ; North East, June 9 — (E. M. Craighead); Charter Oak, July (Author). Recorded as breeding in dead aspen (Populus grandidentata). D. punctulata Sch. | Breeds in dead pine and occurs throughout the pine sections of the state. | _ D. pugionata Germ. S. W. Penna. (Dr. Hamilton) ; Hummelstown, June 12 (Author); Charter Oak, July (Kirk and Knull). Recorded in the literature as breeding ,in living witch-hazel (Hamamelis virginiana), alder (Alnus) and Spiraea opulifolia. D. obscura Fab. Breeds in the dead wood of persimmon (Diospyros virginiana), and can be found throughout the state where the host-plant occurs It is also recorded as breeding in dead staghorn sumac (Rhus typhina). ; D. lurida Fab. A common species which has been recorded as breeding in hickory, blue beech (Carpinus caroliniana) and alder (Alnus rugosa). D. lepida Lec. §. W. Penna. (Dr. Hamilton) ; Rockville, June 1 (A. B. Champlain) ; Hummelstown, July 11 to 29 (Author). Recorded as breeding in dead ironwood (Ostrya virginiana). It was found breeding in the dead wood of hawthorn (Crataegus coccinea) at Charter Oak. Recorded by C. W. Stromberg as hibernating around the bases of haw- — thorn trees. D. scobina Chev. Found in the fall, on the foliage of sour gum (Nyssa sylvatica) in the dead wood of which the insect breeds. The adults hibernate, and can often be found through the winter months. D. americana Hbst. Pittsburgh (H. G. Klages) ; Rockville, Dec., under loose bark (A. S. Koser); Delaware Co., July 12 (H. W. Wenzel); Dec. 13, ~ Jan. 9, State College (Author). D. tenebrosa Kirby. Recorded from New York State, and probably will occur in Penna. D. tuberculata C. & G. S. W. Penna. (Dr. Hamilton); North East, Sept. 2 (E. M. Craighead) ; Hummelstown, July -9 (Author) ; ovipositing in a hemlock (Tsuga canadensis) log at Charter Oak, on June 22. Adults emerged from injuries on living hemlocks at Montebello in July and August. The insect breeds in the dry wood around the injuries on living trees. Poecilonota Esch. P. cyanipes Say. §S. W. Penna. (Dr. Hamilton) ; North East, Aug. 22 (BE. M. Craighead); Milford, June 6 (H. B. Kirk); Charter, Oak, July 8 (Author). Recorded as breeding in large-toothed aspen (Populus grandidentata). P. thureura Say*. This species was found breeding in living willow HE CANADIAN ENTOMOLOGIST. 81 at Harrisburg by A. B. Champlain and the author. The egg is laid on the trunk of the living tree, and the larva, working between the inner bark and outer sapwood, does not travel through the infested tree, but remains at the point where the egg was laid. The rapid growth of the tree furnishes sufficient nourishment. Upon reaching maturity a pupal cell is formed between these two layers, which is surrounded by frass, and very much resembles the pupal cell of Rhagium lineatum. The life history extends over at least two years, since very small larvae, together with mature larvae, were found in the infested trees during the winter months. Adults were reared from May 26 to May 30. Cinyra C. & G. ; C. gracilipes Melsh. SS. W. Penna. (Dr. Hamilton) ; Harrisburg, June (Kirk and Champlain) ; Hummelstown, May and June (Author). Recorded as breeding in white oak (Quercus alba) ; swamp white oak (Quercus bicolor) ; and ironwood (Ostrya virginiana). Buprestis Linn. _ B. sulcicollis Lec. ‘This species has been recorded from New York State. and probably will occur in Pennsylvania. B. striata Fab. Found throughout the pine sections of the state. The adults which appear in the spring, having matured the previous fall, pass the winter in their pupal cells. ‘The species breeds in hard and soft pines, although it was found working in a scar on a living hemlock (Tsuga canadensis) at Hummelstown, and an adult was reared April 1. B. striata var. impedita Say. This color variety occurs with the pre- ceding. ; B. apricans Hbsi. Frankford, July 18 (P. Nell); Tidioute (F. L. - Holdridge). | A secuthern pine species which probably has been imported in p.. lumber. _B. decora Fab. Philadelphia, May to (H. W. Wenzel). 3Brucker, E .A.—Monographie de Pediculoides ventricosus Newport et Theorie des Pieces buccales des Acarines.. Thess presentées a la Faculté des Sciences des a Paris, pp. 355—442, text figs. 1—12, Pls. xviii—xwi. 1i2 THE CANADIAN ENTOMOLOGIST a and it is sadloakitedis the same stage as is represented by the apodous nymph of Pediculoides ventricosus and P. graminum. — - - When we compare the transformations of these other Tarsonemid mites — with those of T. woodi, we can interpret those of the latter in a new light. It is — observed that the transformations of T. woodi are similar to those of the other species here considered, although the morphology of the instars is different, and - undoubtedly its life history will be found also quite different. Here is given an annotated chart illustrating by way of comparison the different instars of the four ; ; EGGS LARVA | NYMPH ADULT | Many produced;}| Represented by , Represented by | Not degenerate never laid; octopod deu'to- apodous ‘initia- in any way. Fac- — Pediculoides about the same|vum stage ofem-, uterine “pupe”’,| ultative preda-_ ventricosus size as newly|bryo; no true} which is really | tors, scavengers emerged ©. larva existing. a Dymph. or parasites, Many produced ; Represented by Pediculopsis about two-thirds | Normal, freeliv-|apodous - nymph | Nob degenerate graminum the size of newily | ing. found inside of | free, sucking emerged ©. old larval skin. | juices of plants. About one-third Represented by 4 Tarscnemus as large as newly | Normal, freeliv-|apodous mnymph| Normal, not de pallidus emerged female; | ing. formed invide of | generate; sucks — iis laid. larval skin. juices of plants: — A very large egg, about the size of | Freelliving but| Represented by | Parasitic (free- Acarapis nongravid fe- degenerate. Two | apodous nymph jliving?); female woodi male; laid in| pairs of legs rep- | formed imside of | somewhat degen-— tracheae of resented by old extra-uterine erate. honey bee. stumps. | larvat skin. + species considered, the comparable, or homologous instars being placed in vertical columns. Degeneration and Adaptation in Parasitic Species. 4A In Pediculoides ventricosus Newport there has been apparently no — degeneration, but on the contrary, in regard to reproduction at least, there has — been great specialization. This specialization has brought about a tremendous — increase in the fecundity of the female and is doubtless correlated with the pre-_ carious conditions that exist in regard to transferance to new hosts. Of those ; females that are compelled to leave their mother and search out a new host — undoubtedly the vast majority must perish. It is seen that the successful female, 3 having once reached a proper host has an abundance of food, hence she can meet the enormous drain placed upon her because of her great reproductive powers. This reproductive power which brings about the swelling of her body during pregnancy to many times its original size, incapacitates her for locomotion, but _ only, it is noted, after she has reached her host. - In Acarapis woodi degenerative changes have already been noted by Rennie j in the shortening of the posterior legs. | This species also shows other evidences ~ of degeneration. ‘The second and third pairs of legs of the larva are not only — reduced, but exist practically as vestiges. | These legs in the free-living species — are usually equal to the front pair and are efficiently functional. The sense | 7? —_ Te 4 THE CANADIAN ENTOMOLOGIST 113 organs, called pseudostigmatic organs, which are so conspicuous and characteristic of the females in the Tarsonemidae are lost in the honey bee Tarsonemid, as was noticed by Rennie. In the male there is little evidence of degeneration. The posterior legs are far from being as well developed as they are in many species, yet are about as large relatively as they are in some free-living forms. All of these degenerative changes observed in A. woodi are most easily explained by attributing them to adaptation to a parasitic life. Other structures also indicate a form of adaptation that the writer has found* to be general in the parasitic Acarina. This is the development of extraordinarily large setae. The female of A. woodi, not only has all the body setae well developed, but two of these located on each of the stumpy, degenerate hind legs are enormous, and in length are about equal to the total length of the body. In regard to the male of A. woodi but little specialization is seen in this respect. Fig. 3. Ventral view of adult female of Podapolipus reconditus R. & G. (After Rovelli and Grassi). In the parasitic family Disparipedidae both degeneration and adaptation -are pronounced. Of the degenerative changes the most pronounced is the shortening of the legs. These may be reduced to mere stumps. _ It is particular- ly interesting to note that in this parasitic family the stumpy posterior legs of the female almost invariably have enormous setae as has been observed in the female of A. woodi. “The limit of degeneration in the Tarsonemidae, and for that matter for all the Acarina, is found in the genus Podapolipus Rovelli and Grassi. In this genus the female (Fig. 3), which is at first hexapod, upon reaching maturity is legless. The male is hexapod. These most degenerate Tarsonemids are found under the elytra of certain Old World beetles. 4Pwing, H. E. (1911). The Origin and Significance of Paraisittism in 'the Acarinia. Trans. Acad- Sci. St. Louis, Vol. xxi, pp. (1-70, Pls, i—vi (Particular referenice, ‘ip. 52). 2 z eh {14 THE CANADIAN ENTOMOLOGIST . an VENATIONAL VARIATION IN RAPHIDIA : a BY NATHAN BANKS, Cambridge, Mass. In r891 Albarda published a revision of this family and it has since been the standard work on the group. In this he uses various venational characters in his tables for distinguishing the species. A few years ago (1918) Navas published a monograph of the family, and gave generic names to the sections of — Albarda and to some he himself separated from the typical Faphidia. Recently in identifying various Raphidians I went over the entire museum collection to see if the venational characters of Albarda and Navas could be utilized to advantage in our species. Having about seventy specimens of ten species of European Raphidia I tested them for these venational characters. As to the stigma. Several European species are separated by having two ~ veinlets in the stigma, and Navas makes a new genus, Lesna, for these forms. _ In several specimens of R. notata one or two wings have a stigma with but one veinlet either forked or simple. In one specimen of R. major three wings have _ a stigma with one forked vein and the other stigma with a simple vein. Both of — these species normally have two veinlets in each stigma. R. xanthostigma normally has but one veinlet, yet in one wing of one specimen in a series of ten there are two veinlets in the stigma. In examining several hundred American specimens | find nine specimens~ in which one or more wings have a stigma with two veinlets; one specimen has it in all four wings; two others have it in three wings; two others in both fore- wings. The position of these cross veins (as in the European specimens) is not constant. Except for these differences in the stigma, five of these specimens are R. oblita, two are R. occulta, one R. adnixa, and one R. assimilis; six are from California, one from Oregon, one from Washington, and one from New Mexico. The five specimens of.R. oblita are not alike in minor venational characters. It is evident that this character is of no generic value, of no specific value in American specimens, and even in the European must be used with caution. Albarda and later Navas makes much of the number of cells behind the — stigma, called the discoidal cells. These are said to be either three, four or five. Three is most common in the European and four or five in the American species. The extra cells usually reach but part way back to the base of the other cells, in fact I have seen no specimens with five complete cells. In the European specimens before me three seem fairly constant for most of the species, but in. FR. notata a fourth cell of varying size is usually present. a In American specimens the number of cells is much more variable. Ina series of eighty R. oblita about half have the second discoidal pedicellate in one or both forewings, and of varying size; sometimes extremely minute, in other — cases reaching to the base of the other cells. And when it is as far back as the other cells its basal width varies from as wide as that of the other cells to a mere— point. In seven specimens there is a fifth cell present in one-or both forewings, of varying size; four of these are from British Columbia, three from California. THE CANADIAN ENTOMOLOGIST Ii5 In thirty-three specimens of FR. adnixa the extra discoidal is often pedicellate, but frequently complete; in two specimens one wing has a small 4 fifth cell. In sixteen FR. assimilis there are none with five complete cells, one or two being pedicellate and sometimes very small, and in one specimen, otherwise agreeing with assimilis, there are but three discodidal cells in each fore wing. . : In fifteen R. astuta four cells are normal, but the second is often es pedicellate, and one with a short fifth cell in one wing. . , In six specimens of bicolor three cells are normal; a fourth is present in __ varying size in three specimens. Two of the Navasian genera are for American _ species having four (Glavia) and five (Agulla) cells, and both distinct from the European Raphidia with three cells. Since this character varies greatly within the various species it certainly is not even of specific, much less generic value. E ‘Navas separates from Raphidia typical those forms having one less apical _) ~vein into a new genus Raphidilla, and Albarda uses a similar character, viz., whether there is a simple third apical vein. In ten specimens of ranthostigma “this character holds, but in notata it varies. When however one tries to apply For of R. oblita and R. occulta nearly one-half of the specimens are not alike in _ the two front wings, in fact it is difficult to find a specimen in which the apical _ venation is even approximately alike in the two fore wings. For example, of the five specimens of oblita having two cross-veinlets in a stigma no two are alike in apical venation. This character is undoubtedly more constant in the European than in merican species, but a character so variable in one part of a genus should _ not be used to separate another part of that genus into a distinct genus. _ Raphidilla is a synonym of Raphidia. he oe the A Another genus of Navas, Subilla, is based on two species (schneideri and 3 _ sericea) with an extra ‘cubital cell. In the two species the extra cell does not widely separated countries. Hagen has suggested that schneideri may be but a _ form of R. cognata, and it is probable that both these species are but venational , variations of some other species. On examining our material I have not found any with the extra cubital cell, but in the allied genus, /nocellia, the number of _ cubital cells varies. Two specimens of Raphidia (one Utah, one Idaho) have 4 but two cubital cells in one wing. The character is surely not of generic value. = _ $till another genus, Puncha, Navas creates for R. ratzeburgi and R. msularis of Europe, on the character of three radial cells in each fore wing. This holds for the few European specimens of these species before me. In DRaphidia there are three radial cells in the hind wing, and in Jnocellia in both “these characters to American Raphidias the result is nothing less than ridiculous. ~ 116 THE CANADIAN ENTOMOLOGIST wings. None of the American specimens examined have more than two radial _ cells. In one specimen of R. ophiopsis there is but one radial cell in one fore ~ wing, and but two in each hind wing. Variation therefore occurs in this character. The two species included in Puncha are very different from each other; one has a simple third apical vein, the other not; one has a long dark ~ stigma, the other a short pale one. It is evident that the two do not form a natural assemblage and that each is more allied to other species. Another genus, Alena, Navas recognizes for two American species, which ~ I had already separated as a section on the number of bullae in the wings. = eS Sa THE CANADIAN ENTOMOLOGIST 117 NEW AND LITTLE KNOWN CANADIAN SYRPHIDAE (DIPTERA) BY C. HOWARD CURRAN, Orillia, Ontario. Syrphus venustus Meigen. This European species, evidently not heretofore recorded from North America, is rather widely distributed, and I have seen specimens from Mass., Wis., McDiarmid, Ont., anda single specimen captured at Orillia on May 30th, 1921, on bloom of Osmorrhiza claytoni in Fitton’s woods, late in the afternoon. In Williston’s table the species would trace out to S$. amalopis O.S., but is readily distinguished. ‘The cheeks and a broad, almost complete, median facial stripe are shining black; eyes short whitish pilose ; antennae wholly reddish, arista black. Thorax and scutellum shining aeneous black with whitish or grayish yellow pile; scutellum subtransluscent reddish-orange in some reflections, and with some black pile apically. All the abdominal bands narrowly interrupted and reaching the side margins; the first pair not arcuate, second and third pairs concave in front; all the bands rather narrow. In the specimen before me the first band does not quite reach the margin, or does so indistinctly, a common variation in this species, according to Verrall. The legs are reddish except the bases of the femora and a black ring on the hind tibiae; terminal tarsal joints brown. Verrall reports the species common in England in wooded districts in spring. I can see no differences between the American specimens and European specimens, from France. Syrphus genualis Will. This species proved to be moderately common this year. Between April 28th and May 25th I took 14 specimens. ‘The earliest specimens were taken on Cowslip in marshes, later on Wild Plum, Black Cherry and Choke Cherry, and a single specimen on Osmorrhiza claytoni. While females predominated both sexes are represented in the series before me. ‘The males have the abdominal bands attenuated laterally. Syrphus cinctus Meigen. A European species which proved to be very abundant this spring on the bloom of Wild Plum and Cherry, but not observed elsewhere. My identifica- tion has been confirmed by Prof. M. \Bezzi, Turin, Italy, who compared specimens with European ones. It traces out to S. diversipes in Williston’s table, but the thorax and scutellum are wholly pallid grayish white pilose, and the abdomen is somewhat shorter. Brachyopa perplexa n. sp. Most closely related to B. notata O. S., but arista not as pubescent and epistoma more produced. Larger than B. media Will., and with black ab- dominal markings, the median longitudinal black line practically complete. Male. Length, 6.5 to8.5 mm. Face and front pale yellow, thickly covered with white pollen, the cheeks and the frontal triangle, except narrowly next to the eyes, shining; a brownish or ferruginous stripe from the eyes to the oral Margin; occiput below shining ferruginous, but above and near the eyes grayish 118 THE CANADIAN ENTOMOLOGIST pubescent. Vertical triangle and a narrow V behind the ocelli on the occiput | grayish yellow (sub-golden) pollinose, the ocellar triangle shining brown. Pile of head; a few pale hairs on the cheeks, posterior orbits with long pale pile be- low, and short black pile arranged in rows, on the upper half. Thorax reddish — brown, the sternum more blackish, but covered with grayish pubescence; disc of the dorsum grayish pollinose, leaving four stripes of a shining dark reddish brown, or sometimes blackish; the median stripes very narrowly separated and expanded posteriorly to unite with the sub-median stripes, which are also entire; the opaque area is strictly confined to the disc. A darker, thickly black pilose stripe runs from the postalar callosities to the suture. Dorsum of thorax — with short black pile, the pleura with longer white pile. Scutellum brownish ~ yellow with short black pile, but with a few slightly longer bristle-like hairs apically. Abdomen pale yellow to luteous yellow, shining; first segment black, its anterior border yellow; sccond segment with a narrow median longitudinal black stripe, narrowly separated from the anterior margin, usually plainly joined to the black of the posterior margin, but sometimes only faintly so, (the median spot is ! shaped without the dot below) ; posterior border narrowly black, sides of segment, except anteriorly, black; third segment similar, darker colored, the longitudinal median stripe and black lateral margins entire; fourth segment similar but usually with the lateral margins more brownish. Hypopygium yel- lowish red. Pile of abdomen fine, whitish, except on apical half of segments two and three, where it is black. Legs reddish brown; tarsi all brown or black- ish, except that the first three joints are yellow apically. Wings slightly yellowish tinged; stigma pale luteous. Squamae clear white, with white pile. Halteres slightly yellowish. In immature specimens taken in early May the ab- dominal markings are more brownish, and in fully mature specimens the abdo- men may be slightly reddish yellow, and is always wholly shining. The thorax ; may be slightly darker or paler than described. , | f ” 3 Female. Averages .5 mm. smaller than the male (the smallest male is 7 mm.) ; face a little more deeply excavated; front shining ferruginous with a very narrowly interrupted whitish pollinose band below the middle; stripe on cheeks faint or absent; median abdominal stripe boarder, complete on segments | 2 to 4 inclusive; transverse bands broader and successively narrower distally; fifth segment yellowish ferruginous with the narrow hind border blackish and the lateral margins ferruginous or brownish. The general color is more ferruginous _ than in the male. “ Holotype, 8, Orillia, Ont., June 2, 1921; Allotype, 9, Orillia, June 2, 1921, in the Canadian National Collection, Ottawa. ‘ Paratypes, 43 specimens, the majority males, Orillia, May 8th to June i 14th, 1921, (Curran) on bloom of Choke Cherry, Black Cherry, Wild Plum, in vicinity of woods, and on bloom of Osmorrhiza claytoni in open sub-swampy woods. B. perplexa differs from notata O.S., in the shorter pile on arista, darker — thorax and abdominal markings and darker ground color of body, more pro- : duced face, as well as in the unclouded wings. From media Will it differs in the more reddish color, more produced face, darker abdominal markings; from % ! j 4 a THE CANADIAN ENTOMOLOGIST 119 flavescens Shann. in the same respects and in the darker thorax; from gigas - Lovett in its smaller size, less pilose arista, paler color, and in thoracal and abdominal markings. It differs from the remaining species by lacking pollen on the abdomen, except perhaps on the first segment. Helophilus lunulatus Meigen. : This species was abundant at Cowslip at Orillia during the first week in May this year, (1921) and over 40 specimens were taken, including only three females. My dates range from April 28th to May 22nd. Other bloom on which taken were: Wild Plum, Choke and Black Cherry. It was abundant only on Cowslip. Brachypalpus apicaudus n. sp. Male. Length, 13 mm. Head shining black, the face and front obscured _ by yellowish pubescence, leaving onlv the cheeks shining. Face in profile retreat- ing to below the middle, thence slightly produced to the tip of the oral margin; first antennal joint piceous, second luteous, third black, its base yellow below, arista yellow, its tip blackish. Eyes very slightly separated; frontal triangle black, with black pile in front; posterior orbits and narrow facial side margins with rather long yellowish pile. Thorax and scutellum aeneous greenish black, moderately short fulvous pilose. Abdomen greenish black, its disc with short, its margins with longer fulvous pile. Apex of fourth segment emarginate in middle, its end reddish yellow. Legs black, tips of femora, bases and tips of the tibiae and the basal three joints of the tarsi yellowish. Legs fulvous pilose except the arcuate hind tibiae which are clothed with short blackish pile. Wings slightly infuscated anteriorly; stigma pallidly yellow. Holotype, ¢&, Cranbrook, B.C., (C. B. D. Garett), in the author’s collection. This species is very closely allied to B. inarmatus Hunter, but the thorax is only slightly purplish, the second segment has a metallic bluish reflection and no distinct opaque spot; the legs are more yellowish and the antennae distinctly darker; the hind tibiae terminate in a stout spur. Mailed August 4th, 1922. “A Che Canadian Entomologist Vor. LIV. ORELELTA, RE, To22, No. 6. POPULAR AND PRACTICAL ENTOMOLOGY Tir Conrror, oF INsEcts LIABLE TO BE IMPORTED IN RAILWAY Cars BY R. C. TREHERNE, Entomological Branch, Department of Agriculture, Ottawa. The desire to check the increase or to prevent the establishment of insect pests in British Columbia has always been one of the main objects of economic entomologists and horticultural field inspectors in pursuit of their official duties. This object has been especially emphasized as regards fruit-infesting insects for the reason that horticulture and the cultivation of fruit has been considered, in the past, the “first arm’ of the agricultural industries of the Province. The Codling Moth is particularly classed as an undesirable insect pest of apples and pears, liable of importation into any given fruit-growing section, and it 1s with this insect and its control that this article has special reference. As a matter of general information, the Codling Moth, until the present day, has not become generally distributed throughout the fruit-growing areas of the Province, neither is it as yet regarded as an insect which requires attention as a regular established orchard pest. There are between 30,000 and 40,000 acres of fruit in the Province of British Columbia, three-quarters of which acreage is located in that part of the Province known as the “dry Interior’ where irrigation is commonly practised, and of this 20,000 acres close upon 850 acres were under quarantine at the close of the year 1921, but it is probable that not much more than 300 acres were actually infested with the Codling Moth. Where this insect occurs the control operations are under Government surveillance, the burden of control not having as yet been thrown upon the shoulders of individual growers. This is an interesting point for the general information of entomologists, but in as much as the Codling Moth does occur in the province to a somewhat limited extent the problem of control may be and has been considered under two distinct phases. (1) The control of the-insect within the Province. (2) The closing of the avenues of importation. The first phase detailing the stringent regulations which govern an area under quarantine by Government, has been dealt with on other occasions. It will not be necessary to mention this information again at this time except to state that the control operations are strictly based upon eradicative procedures and that total eradication of the Codling Moth has been successful in eight outbreaks out of twenty that have occurred until the present time. The following table indicates the degree of success that has attended the operations on the present infested areas as it affects the fruit growing areas of the Interior. 122 THE CANADIAN ENTOMOLOGIST TABLE 1, Showing the number of larvae of the Codling Moth taken im British Colum- bia in the fruit-growing areas of the Okanagan and Similkameen Valleys and points on the main line of ‘the Canadian Pacific Railway east from North Bend, Acreage under Number of larvae Year quarantine and pupae taken — 1915 335 10,000 1916 330 3,500 1917 330 600 1918S “37> 394 1919 FOO 873 1920 G45 174 1921 S50) approx, TS5 The second phase of the problem is as important as the first and in a much as certain lines of study in this connection have been conducted, which have now reached a certain stage of finality, this article has been written to illus-— trate not only the stage of development of the fruit industry of British Columbia, the centres of outbreak of the Codling Moth, but also the means and methods of introduction of this pest with suggestions for preventing its further importa- tion, According to the Market Reports and the Agricultural Records of the Department of Agriculture but particularly from a brief prepared under the direction of the British Columbia Fruit Growers Association before a sitting of a Federal ‘Tariff Commission in September, 1920, the following statistical data are noted. ; In 1891 the fruit industry of British Columbia boasted approximately 450,000 fruit bearing trees; in 1901, 649,091; in I91I, 2,677,486; in 1913, 2,978,903; while in 1920, 1,165,309 apple and pear trees alone were producing fruit in the Okanagan and Similkameen Valleys and at points on the main line of the Canadian Pacific Railway east of North Bend. The production of apples far outdistances, in numbers, the quantity of other tree fruits grown, repre- senting 77 per cent of all trees planted. The yield from these trees is recorded as follows: FHIO® ss Coke at ee 210,000 boxes of apples IOTIS .nan ek ae 250,000 1OU 4s se phe eae 430,000 LOT Sac. Sato te 477,000 IOLA. cash pe col cz devant O85 ,000 165.0 tea ea 787,750 1Q1G 54 SRR 1,289,980 Aa) & Par ae eA 1,502,921 IOLG. wien ie ee 1,343,450 POI. a8 THE CANADIAN ENTOMOLOGIST good fortune, I found them again. Later, in February and March, I discovered — them around the roots of beeches in a neighboring wood; and in April I sifted a a few out of moss on the rocks where they first appeared. They were never in — great numbers, and it usually took about an hour’s steady search to gather in a dozen individuals. “| Achorutes nothus n. sp. Color dark blue; cuticle finely tuberculate. Eyes (fig. 1) eight on each side. Postantennal organ (fig. 1) with four peripheral tubercules. Antennae — three-quarters length of head; segments as 5: 15: 15: 22; at apex clavate pro- trusible sense organ (fig. 2) and nine or ten “olfactory” hairs; on outer side of third segment distally a small organ of two curving rods with two stout guard ~ hairs (fig. 2). Unguis (fig. 3) long, curving, unidentate on inner margin one a third from tip. Unguiculus not quite half as long as unguis; broad lamella at © base, apex sharp rounded. One tenent hair feebly knobbed surpassing end of — unguis. Distally on tibiotarsus several knobbed hairs bent apically. Dens — (fig. 4) short and stout, swollen and rounded apically with four or five conical teeth dorsally ; mucro inserted on inner side of apex of dens, one quarter lengta of dens, apically slightly curved with one large tooth as fig. 4. Anal spines ~~ (fig. 5) one third length of hind unguis on low papillae. Tenaculum (fig. 6) quadridenticulate. Clothing (fig. 7) stout curving serrate setae, and long capi- tate setae with a few small serrations, those on posterior segments more strongly _ knobbed than those towards head. Maximum length 1 mm. Found on snow ~ November to March; and in moss on rocks in April, at Arnprior, Ontario, Canada. ~ Dr. J. W. Folsom, who kindly examined these insects for me, points out — that the claws, anal spines, and furcula closely resemble the corresponding organs 7 of Achorutes socialis, but the teeth on the dentes are fewer and do not shade off — into smaller teeth as in socialis. The clothing of serrate and capitate hairs how- ever is very like that of Achorutes packardi, a species which rarely if ever — comes out on the snow, although sometimes to be found in midwinter under bark _ or walking around on stumps. 4 In the field Achorutes nothus may be distinguished by its small size, but this is no great distinction, as A. socialis of 1 mm. in length are also not in- frequently seen on the snow. The other new Achorutes here described was forwarded to me by the Dominion Entomologist for identification, having been sent into the Entomo- ; logical Branch by Mr. Ricker, of Monteith, Ont. They were collected by the — Monteith station agent, Mr. J. D. Allen, from a space of a few square feet on his lawn, where they appeared in such numbers that nearly half a cupfull was ~ gathered with the aid of a spoon. They had apparently come out of the soil, as Mr. Allen tells me there was no rotten wood or debris in the vicinity that might have sheltered them. And alas! how often must the innocent suffer with the guilty. The harm- less Achorutes was sacrificed for the evil deeds of the cutworm and the locust. — Having in mind the destructiveness of insects in general, Mr. Allen was doubtless — alarmed for his lawn when he saw this horde of Achorutes. He writes in 1921: ; THE CANADIAN ENTOMOLOGIST 153 be “The balance of the insects were destroyed with coal-oil, and to date have not noticed any more.” . ™ “mad Achorutes pannosus n. sp. a Color dark blue; as material was received in bad condition cannot say if uniform or mottled. Cuticle finely tuberculate. Eyes (fig. 8) eight on each side. Postantennal organ (fig. 8) w ith four peripheral tubercules. Antennae four-fifths length of head; segments'as 5: 10: 10: 15; at apex protrusible clavate De sérise organ (fig. 9); also five or six curved “olfactory” hairs; distally on outer _ side of third segment, a small sense organ of two short curving “pegs” in little : _ pits with two stout curved guard-hairs (fig. 9). Unguis (fig. 10) stout, curving, : -unidentate i in apical third. Unguiculus acuminate, about half as long as unguis. _ Tenent hair, one with small knob, not extending to end of unguis. Dentes two ; and one-half times as long as manubrium, with large dorsal tubercuies distally. ~ Mucro (fig. 11) one third length of dens, hooked apically with wide lamella j or in a small percentage of specimens, not hooked apically with narrow lamella asin fig. 15. Anal spines (fig. 12) one third length of hind unguis, on promin- ent papillae about same length as spine. Tenaculum (fig. 13) quadridenticulate. _ Clothing (fig. 16) a very few short simple setae. Maximum length 1 mm. a -_ - Achorutes pannosus comes close A. maturus Fols. but differs in the pres- 4 ence of large dorsal tubercules on the dentes, broader base of unguiculus, longer i; anal spines, and in the shape of the mucro, as well as some other minor differ- ences. The species also approaches the European A. manubrialis Tullb. but is separated from the latter principally by differences in mucrones, unguiculus and _ postantennal organ. EXPLANATION OF PLATE 2 1. Achorutes nothus, eyes and postantennal organ of left side, x 570. 2 . . olfactory hairs and sense organs of right antenna x 400. 3. ae = right hind foot x 500. 4. - i lateral aspect of dens and mucro x 420. AY Aa left anal spine x 500. 6. i; i tenaculum x 560. a = clothing of first abdominal segment x 480. 8. Achorutes pannosus, eyes and postantennal organ of right side x 600. 9. 2 . olfactory hairs and sense organs of left antenna x 600. ; 10. * right hind foot x 530. 15 re 2 lateral aspect mucro and dens, principal type, x 1,000. 1. t n anal spine x 600. s Seated * tenaculum x 600. T4. " 4 dorsal aspect, variant form of mucro, x 1,000. 15. = ae lateral aspect, variant form of mucro, x 1,000. 16, 4 7 clothing of first abdominal segment x 500. 154 : THE CANADIAN ENTOMOLOGIST. SEXUAL ATTRACTION OF THE FEMALE HESSIAN FLY* yi (PHYTOPHAGA DESTRUCTOR SAY) ase / BY W. B. CARTWRIGHT, . = Scientific Assistant, U. S. Entomological Laboratory, West Lafayette, Ind. An accidental observation on April 2, 1921, at Centralia, Illinois, prompted — a short study of the field activity of the male Hessian fly. On this date a female 4 fly, emerging from a flaxseed partially covered by mud, became entangled and _ stuck, but was not so hidden as to evade the courtship of a number of male flies. A miniature swarm attended the female. Three and four males made offers of copulation at the same time while others stood facing thé female or walking and ss flying impetuously about until an opportunity came to replace the ones in closer touch with her. - Following the clue given by the helpless female fly, several small cylin- — drical cages one inch in diameter and three inches tall were stocked with newly emerged females of known age, care being taken to obtain individuals which were — still soft, uncolored, and unfertilized. Five females were imprisoned in each cage and the cages placed on the surface of the ground in the field as desired. OBSERVATION I. Five cages containing females were placed in the field. Over aoe cage was placed a larger wire cage three inches in diameter and ten inches tall painted with tanglefoot. These cages were placed at 9 a. m., April 2, and the males — excited by the presence of the females, were caught, counted and removed — as shown in Table 1. The females were left undisturbed until the males failed to be attracted. On April 4 only one female fly was alive in each cage and the following day all were dead. . TABLE I. Date Hour Cage 1 Cage 2 Cage 3 Cage 4 Cage 5 Total — Apr. 2 10 a. m. 43 159 43 99 86 430 11 a. m. 50 103 51 60 138 402 4 p.m. 42 91 SO 39 20 Pap ae Apr. 3 9 a. m. 190 140 . (240 145 ST 802 liars: 142 S1 126 109 43 501 4 p.m. 11 15 12 32 10 SOs Apr. 4 9 a.m. 57 “e126 118 169 SO 5503 11 a. m. 46 61 56 40 18 221 4 p. m. 9 8 29 6 3 55 Apr. 5 9 a. m. 93 32 17 AT 45 234 14sa- ae 0 0 0 0 0 On 4p. m. 0 0 0 0 0 ; 20 Apr. 6 9 a.m. 24 15 5 17 3 64 25 11 a. m. 0 0 0 0 0 0 4 p.m. 1 0 0 1 3 5 Apr. 7 9 a.m. 0 1 al, 1 8 i ke 11 a.m 0 0 0 0 0 0 z 4p.m 0 0 0 0 0 0" = Total TOS 832 778 T65 do+ 3627. The results show that an average of 145 males were attracted for each of the 25 females confined. In thé case of the five females in Cage 2, a maximum average of 166 males per female was obtained and in Cage 5 a minimum average | *Published by permission of the U. S, Secretary of Agriculture. ond : 4 THE CANADIAN ENTOMOLOGIST ; 15h. of 109 males per female was obtained. It was noted during the observation that the males advanced against the wind and the advance was made slowly from a general assembly area a short distance from the females. The attraction to all cages continued even after all females were dead. The greatest number of males were caught on the cages just above the ground surface, thence upward for three inches. The activity of the males was most manifest early in the morning. aa OBSERVATION 2. oe & . _ To determine the area of attraction and the limits of the zone of advance _ or assembly, three cages, numbered 1, 2, and 3, were placed in the field in separ- ated places. Concentric circles were marked around all the cages with radii one ies fifteen feet. The leeward arcs of ninety degrees were the observational limits _ of cages 1 and 2. For cage 1 the arcs were set with screen wire painted with _ tanglefoot and for cage 2 set with tanglefoot painted in one inch strips on the _ ground. For cage 3 the concentric circles were used for points of position only, the observations being centered on the side of the sector set with tanglefoot sereens enclosing an arc of forty-five degrees on the leeward side of the cage. _ The observation started at 10 a. m., April 3, and ended the same day at 3 p. m The number of males caught in the tanglefoot at one foot intervals from one to fifteen feet, is shown in Table 2. TABLE 2 li1/2)3 ~4)516]7|8 | 9 | 10] 4a | 12| 13 | 14 | 15 |Lotal 35| 15] 2 4| 18] 12] eae v/o 0/0 89 35| 25| 37] 26] 42] 40| 1019} 4/2171/51[3]1)]0]| 246 87/116) 18) 15) 10) 4 eee 270 Males caught-— Pty RE eS Se ee es | 45).70] S617) 17)11|3)7)5)/3 1/4] 0] 605 Total [175|156| 57 5 Males within fifteen feet of the females were apparently attracted and definitely so within ten feet. The zone oi assembly was particularly outlined i “from one to six feet from the females. Fs During the time the cages were run in both observations the wind was in. fa constant south and south-west direction with a velocity of six to eight miles per hour and a maximum not over twelve. Fly emergence in the field was at its _ maximum intensity for the season and the weather clear and warm. A NEW PARASITE OF THE SPRUCE BUDWORM (HYM). . BY S. A. ROHWER, U. S. Bureau of Entomology, Washington, D. C. The following description of a new species of Phytodietus, reared by Mr. Ex. B. Baird as a parasite of the spruce budworm, is presented at this time so the name may be used in a forthcoming paper dealing with this moth. ; og Phytodietus fumiferanae new species Allied to Pirytodietus annulatus (Provancher) from which it may be dis- ‘t guished by longer postocellar line, dark hind legs-and different colored coxae of the male. -~Female.—tLength, 8 mm. ; length of antenna, 8.5 mm.; length of ovipositor beyond abdomen, 3.5 mm. Slender; clypeus depressed medianly along anterior 150 : THE CANADIAN ENTOMOLOGIST. ; margin, which is slightly emarginate; area between eyes but little higher than — broad; eyes nearly parallel within; face finely granular, frons more finely so; postocellar line nearly twice as long as the ocellocular line; depressed areas of scutellum and metanotum without sculpture; propodeum shining with a faint — median depression ; anterior basitarsus about two-thirds the length of their tibia; calcaria of hind tibia but little less than half as long as hind basitarsus; abdomen shining, the second tergite but little longer than the third. Black; palpi, mandibles (except apices), small spot on inner superior orbits, usual spots on scutum, tegulae, small spot below hind wings, two small spots of anterior margin of scutellum and a larger posterior spot, median spot of metanotum, interrupted V-shaped line on posterior face of propodeum, and narrow apical margins of tergites, whitish; legs rufous; trochanters whitish; basal part of hind trochanters, hind femur, except rufous mark beneath, hind tibiae except extreme white base, and hind tarsi black; wings hyaline, iridescent, venation dark brown, stigma yellowish medianly. fe Male—tLength, about 7 mm.; length of antenna, about 8 mm. Differs in color from the female as follows: head below antennae, scape beneath, proepi- sternum and lower lateral margin of pronotum, four anterior coxae, mesosternum and lower part of mesepisternum, yellowish-white; hind coxae black above, yellowish-white beneath. Type locality—tLillooet, British Columbia. Described from two females (one type) and one male (allotype) reared by A. B. Baird from cocoons collected July 11, 1919. The male issued in the laboratory February 7, 1920, and the females February 9, 1920. Host.—Spruce budworm, Tortrix fumiferana Clemens. Type and allotype—Cat. No. 23068 U. S. N. M. Paratype.—Canadian National Collection. Norges on Coccrpar. IX. (Hemiptera), BY G. F. FERRIS, Stanford University, Calif. The present classification of the genera of the subfamily Coccinae (or Lecaniinae) is based for the greater part upon the nature of the secretions and only to a small extent upon the morphological characters of the insects them-. — selves. Some justification for this is to be found in the fact that the secretions — present a wide range of form while in the more conspicuous features of their morphology the many species of the subfamily are, with but few exceptions, — extraordinarily conservative. However, I can not believe that any really satis- factory classification can be arrived at until an exhaustive study of the insects themselves has been made and the facts thus obtained have been correlated as — far as may be with the more easily observable facts of habit and character of the secretions. On the other hand, I am somewhat inclined to believe that a complete y correlation of this sort can not be obtained for it seems probable that some of - the differences in the nature of the secretions are in part due to differences 1Continued from Canadian Entomologist, 53: 95, (1921). THE CANADIAN ENTOMOLOGIST. 157 _ in the physiology of the insects and not in their structure. In such cases it would seem entirely proper to give due consideration to such factors in attempting to arrive at a natural arrangement of the species. Genus Takahashia Ckll. The original description of this Soe (as a subgenus of Pulvinaria) includes merely the following statement, “Similar to ordinary Pulvinaria in Be eral structure but forming a very long, firm ovisac, which projects from the twig in a curve about 17 mm. long, carrying on its end the shriveled body of the _ female”. ma = = J cs 3 one E hf Pig. i. Takahashia japonica Ckll.:A,—anal plates of adult ; B,—tubular duct ; C,—antenna a of adult; D.,—anal plate: of first stage: E,—margin al setae of adult; F,—antennae of first stage : ; G.—stigmatic setae of firs stage: H.—anterior tarsus of adult, ® 4 a I have at hand material of 7. japdnica Ckll. and 7. jaliscensis Ckll., the ~ former being the type of the genus. On the basis of the type species I would - define the genus as follows. ° . Coccidae referable to the subfamily Coccinae (of the Fernald Catalogue) ; = and legs well developed, the former tending to be rather short; marginal _ setae present ; stigmatic clefts practically obsolete, the stigmatic setae but little or _ not at all differentiated ; anal plates of ordinary form, anal ring with eight setae; ; de m remaining membranous at maturity, beset dorsally with relatively few, simple pores and a few small, tubular ducts, ventrally with great numbers of circular, multilocular pores and tubular ducts. In life with the dorsum practically re of secretion; at maturity secreting an ovisac. ; On the basis of this characterization T. jaliscensis Ckll. could not be referred to this genus for the dorsum is beset with numerous small, 8-shaped pores. However, until a better understanding of generic limits has been attained - may well remain here. 7. citricola Kuwana, as far as I can see, is simply a 158 : THE CANADIAN ENTOMOLOGIST. ee. Pulvinaria, having the stigmatic setae strongly developed as in the latter genus. __ 5) > > oe a Whether Takahashia can really be maintained as distinct from some of the other genera of the same general type, such as Lichtensia and Philephedra, is a matter that will require much further study to settle. Takahashia japonica Ckll. (Fig. 1.) Material Examined. From various hosts in Japan, being the material recorded in Kuwana in 1902. Notes. The antennae (Fig. 1C) are well developed but rather short and stout. The legs are likewise well developed, although rather small, the © tarsal claw and digitules quite slender. According to Cockerell the anterior tarsi are apparently two-segmented. While this condition appears to be quite constant, it appears to be due merely to a fold and not to a genuine segmentation (Fig. 1H). The marginal setae (Fig. 1E) are quite large, stout and sharply pointed and are arranged in a definite single row. ‘The stigmatic setae, if differentiated at all seem only to be slightly stouter, and at times slightly smaller than the marginal setae. "The anal plates (Fig. 1A) are of quite ordinary form, but somewhat variable. ‘The ventral side of the body in the abdominal region bears great numbers of circular, multilocular pores and a sub-marginal zone of cronee’ tubular ducts of the type shown in Fig. 1B. 3 The first stage has the antennae (Fig. 1F) rather slender, five-segmented. The marginal setae are very few, small and filiform and the stigmatic setae, three in each group, are small, stout, conical and equal. The anal plates (Fig. 1D) are somewhat reticulate. Fig. 2. Takahashia jaliscensis Ckll.: A,—anal plates of adult; B,—S-shaped pore from > f dorsum; C,—circular pore from dorsum; D,—stigmatic setae of first stage ; B— anterior tarsus of adult; F,—antenna of adult; G,—tubular duct; H,—stigmatic. 4 setae of adult; I,—amntenna of first stage. Takahashia jaliscensis Ckll. (Fig. 2). Material Examined. A slide mount, labeled “type” received through the — kindness of Professor Cockerell. : is TIE CANADIAN ENTOMOLOGIST. 159 Notes. ‘This species resembles 7. japonica in having the antennae (Fig. _ 2F) rather short and stout, but they have six instead of seven segments. The = legs are much larger and stouter than in japonica and the claw (Fig. 2E) i out. The tarsus is but little more than half as long as the tibia. The seal ~ Be rinas are arranged in a definite single row, are rather stout, tapering and sharply pointed ; the stigmatic depressions are very shallow, the stigmatic setae (Fig. 2H) short, stout, but slightly tapering, with blunt tips, subequal. The depressions are - connected with the corresponding spiracles by a rather broad zone of circular “pores. The anal plates (Fig. 2A) present no peculiarities. _. The dermis membranous, beset dorsally with numerous very small, 8- _ shaped pores (Fig. 2B) and with larger, circular pores (Fig. 2C) which are "concentrated in a median area, particularly in front of the anal plates. On the ventral side there are great numbers of circular, multilocular pores in the _ abdominal region, together with a zone of very small, tubular ducts (Fig. 2G). The first stage larva has the antennae (Fig. 21) rather slender, five seg- _ mented. The marginal setae appear to be lacking; the stigmatic depressions bear. three setae of which the cephalic is quite large and long and the other two very small (Fig. 2D). The anal plates have very much the same form and appear- ace as in the adult but bear a very long apical seta. Fig. 3. Pseudophillippia quaintancii Ckll.: A—anal plates of adult ; B,—1eg of adult; C— §-shaped pore of dorsum of adult; D,—antenna of first stage: BH— anal plates of first stage; F,—ant-nna of adult; G, —stigmatic setae of first stage. Genus Pseudophillippia CkIl. The original description of this genus is merely the following: “A niine Coccid with, in the adult ¢, rudimentary legs and antennae ; secreting a profusion of cottony matter, which completely covers and hides it. Skin not I rewrite this description as follows: Coccidae referable to the subfamily Coccinae (oi the Fernald Catalogue) ; 1 the antennae and legs very greatly reduced, but retaining their segmenta- , the antennae apparently four-segmented; with tlie stigmatic depressions flete and the stigmatic setae ee ng; without marginal setae; with the dorsum kly beset with rather small, S-shaped pores borne at the i inner end of short . In life with the dorsum ae covered with fluffy, white secretion; not eting an ovisac. 160 THE CANADIAN ENTOMOLOGIST Pseudophillippia quaintancii Ckll. (Fig. 3). Material Examined. From Pinus sp., Parksley, Virginia. Notes. Antennae (Fig. 3F) very small, but with the segmentation fairly distinct, the specimens examined showing them as four-segmented. Legs (Fig. 3B) likewise very small but with the segmentation normal. Marginal setae and stigmatic setae apparently entirely lacking. Dorsal pores extremely abun- dant, upon careful examination showing as definitely 8-shaped and borne at the inner end of a short duct (Fig. 3C). Venter apparently without circular multi- locular pores and with tubular ducts, if present at all, very few. Anal plates (Fig. 3A) roughly circular in outline, setae distributed as indicated in the figure. Derm but slighlty chitinized. First stage with the antennae (Fig. 3D) quite slender, five-segmented. Derm beset with many small, 8-shaped, sessile pores, these arranged in transverse rows on the abdomen. Marginal setae very few and small; stigmatic setae three in each group, very small and slender, the median seta slightly longer than the others. Anal plates (Fig. 3E,) of ordinary form. Cryptostigma new genus. Coccidae referable to the subfamily Coccinae( of the Fernald Catalogue) ; with the antennae and legs vestigial; spiracular depressions very deep and with the base surrounded by a conspicuous, heavily chitinized, crescentic dorsal plate which is thickly beset with small pores; spiracles very large, lying directly beneath these plates; stigmatic setae lacking, marginal setae present; derm for the most part membranous, beset dorsally with many minute, simple pores and ventrally with a relatively small number of multilocular pores; anal ring with ten setae. In life, as far as observed, with slight dorsal secretion and without an ovisac. Type of the Genus. Cryptostigma ingae n sp. Notes. ‘The combination of characters given above distinguishes this genus very markedly from any other that has been described. The position of the spiracles, directly beneath the end of the stigmatic clefts is especially peculiar. Cryptostigma ingae n. sp. (Fig. 4) Type Host and Locality. From Inga Laurina, “guama,” Lares, Porto Rico. Habit. Occurring inside the hollow twigs, attended by an ant, Myrme- lachista ambigua ramulorum Wheeler. In the specimens examined the dorsum bore but a small amount of secretion and there was no evidence of an ovisac. From each stigmatic cleft, however, there arises a thick pencil of white wax. Morphological Characters. Length (on slide) 2.4 mm. Derm mem- branous throughout except for a narrow area encircling the anal plates and the plates at the base of the stigmatic clefts. Antennae (Fig. 4C) very small, indistinctly aiinice Sete Legs reduced to unsegmented vestiges, which, however, still retain the claw (Fig. 4). Plates at the base of the very deep stigmatic depressions (Fig. 4G) heavily chitinized and thickly beset with small pores. Spiracles very large. Marginal setae (Fig. 41) small, conical, arranged in an irregular single row. Anal plates (Fig. 4B) relatively very large, together forming an elongate oval, each with several small setae above. ‘The con- dition of the specimens does not permit the determination of the ventral charac- 4 | | 4 ) : g : : J THE CANADIAN ENTOMOLOGIST. 161 _ters of the plates. Anal ring very small, lying beneath the anal plates and apparently with ten setae. Dorsum with none but small, simple pores with chitinized rim. Venter with a relatively small number of circular, multilocular oe (Fig. 4D) in the genital region. Fig. 4. Cryptostigma ingae n. sp.: A—adult; B.—anal plates and surrounding region of adult; C—antenna of adult; D—circular pore of venter of adult; E,—marginal seta; F,—anterior leg of adult; G,—plate at base of stigmatic depression; H.— Stigmutic depression and spiracle of first stage; L—antenna of first “tage, - First stage with the antennae (Fig. 41) quite slender, six-segmented. ~ Marginal setae extremely small, filiform, quite numerous. Spiracles close to the lateral margin, the stigmatic depressions well marked, with a single stout seta on the anterior margin. Anal plates set in a deep cleft, in general form much as in the adult but bearing a very long seta at the apex. ' Notes. For the material of this interesting species I am indebted to ‘Mr. G. N. Wolcott, Entomologist of the Insular Experiment Station at Rio Piedras, Porto Rico. 162 THE CANADIAN ENTOMOLOGIST. NEW SPECIES OF THE OLD GENUS LEPTURA AND ALLIED GENERA (COLEOP.) BY RALPH HOPPING, Dominion Entomological Branch, Vernon, B. C. The flora of California is unique, in that most species are found only within the boundaries of the state and some are so localized as to occur only within the boundaries of one county. ‘This is not confined to annuals and flower- ing shrubs. Many of the conifers and oaks are extremely local in their distribu- tion, and are undoubtedly remnants of a former flora, which owing to sheltering circumstances or the adaptability of the individual has persisted and flourished under new conditions. It is, therefore, small wonder that the insect fauna presents many localized species, where so many different food plants exist with limited distribution. For the past year Dr. J. M. Swaine and the author have been making an exhaustive study of the old genus Leptura as embraced by Henshaw’s “Check List of the Coleoptera” and divided into 13 genera by Leng’s “Catalogue of the Coleoptera of North America, North of Mexico.” Pending the publication of this revision it seems advisable that the following new species be referred to under the generic name Leptura. These species seem very local in their dis- tribution, as is no doubt the case with Van Dyke’s Leptura scapularis and Fall’s L,. subcostata and L,. kernii of all of which I have seen the types. I wish to express my thanks. to Mr. C. A. Frost of Framingham, Mass., for kindly comparing some of these specimens with the Le Conte types, and for his examination of 1. rhodopus Lec. which, in Mr. Frost’s opinion, is a distinct species with the legs reddish and not black as stated by Leng; although the original description states “feet bright ferruginous” the tarsi are black. Leptura isabellae n. sp. A small, robust species, entirely black except the elytra which are maculate ; dorsal and ventral surface subopaque and rather closely covered with pale, coarse vestiture, longer on the head and prothorax. The head coarsely, irregularly punctate, slightly narrower than the pro- thorax and moderately depressed between the eyes; antennae filiform three- fourths the entire length of the insect in the ¢, one-half that length in the @ and somewhat stouter. The prothorax as wide as long; margins evenly rounded in outline, nar- rowing strongly at apex, anteriorly and posteriorly margined; anterior and posterior transverse impression feeble; basal angles subacute, pronotum coarsely punctate and strongly convex; intercoxal piece linear. The elytra ferruginous, sparsely punctured, broader than the pronotum, gradually narrowed from base to apex; with black maculations, each elytron having a black, circular, noticeably concave spot at the posterior portion of the basal third, aproaching but not quite meeting the sutural margin, a black spot in the same relative position attaining the outer margin, a larger postmedian black spot, distant from the suture but extending to the outer margin, the suture, yh “ay OE ANY i 0 Mh Me hE eae THE CANADIAN ENTOMOLOGIST. 163 outer margins and apices black, vesture sparse and coarse, pale on the ferru- ginous portions, black on the maculations; apices subtruncate. The hind tibial spurs long; legs and antennae in ¢ longer than in @ ; metasternum bidentate in 4°; metepisternum sides parallel, broad (width one- third length) ; female stouter than male. Length, 6,7 mm.; 2,8 mm. Five males and two females examined, four (2¢ ¢ and 22 @ ) collected at Isabella, Kern Co., Calif., in 1913, two (4 ¢) collected at Waltham Cr., Fresno Co., Calif., in 1907, and one ¢ given me by Mr. F. W. Nunenmacher, collected in Esmeralda Co., Nevada. ‘The elytra of the Waltham Creek and Nevada specimens are testaceous instead of ferruginous, the Nevada specimen - having also testaceous femora. Type, a male in the Canadian National Collection, Ottawa; Paratypes, 4 and ¢, in the collection of the author, all from Isabella, Calif. This species should be placed probably just before L. sexpilota, from which it may easily be distinguished by the position and concavity of the basal, discoidal, black spot, the shorter form, and sparser vestiture. — Leptura isabellae seems to be found only in the semi desert regions of California and Nevada. j Leptura swainei n. sp. A small stout species, opaque, black, except the legs and antennae, which are bicolored. The head is coarsely punctate, slightly narrower than the prothorax with vestiture sparse and pale; antennae filiform, brown except the scape which is testaceous. The prothorax is slightly longer than wide; vestiture long, sparse, pale and moderately fine; pronotum coarsely and irregularly punctate, sides sub- angulate just anterior to the middle, narrowing to the apex which is margined, basal margin canaliculate with channel shining; basal angles acute; intercoxal piece linear. : The elytra are black, opaque, with short black vestiture ; the sides parallel ; convexly rounding the apices, which are obliquely subtruncate. The legs have the femora testaceous and tibia and tarsi brown; metepister- num wedge-shaped, metasternum not dentate in ¢. Length, ¢ 7.5 mm.; 2 8 mm. Type, a male, in the Canadian National Collection, Ottawa; one Paratype, a female, is in the author’s collection, both collected at Kaweah, Tulare Co., Calif., at an elevation of 1000 feet in the foothills of the Sierra Nevada Mts, by the author in 1892. This species should come immediately after L. sexpilota but may easily be distinguished by its black elytra with short vestiture, shape of prothorax, elytra with convexly rounded apices, and absence of teeth on the metasternum of the male. The female is larger and more robust than the male. Leptura lucifera n. sp. Of medium size, wholly black, except the elytra which are red; ventral 164 THE CANADIAN ENTOMOLOGIST. aspect shining; dorsal aspect feebly shining, with a peculiar dull sheen to the elytra. The head is black, as wide as the prothorax, coarsely punctate, abruptly constricted behind the eyes, with transverse impression, front steep, strongly impressed between the antennae. Antennae black, two-thirds as long as body, scape enlarged at apex to twice the width of second segment, third and fourth segments linear, 5th widened at apex to twice its basal diameter and flattened, segments 6 to 11 wide and flattened. The prothorax black, coarsely punctate, slightly and evenly narrowing to apex which is margined, basal angles obtuse, base not margined, bisinuate, with a short basal transverse impression, narrower than base of elytra; sides slightly constricted immediately anterior to basal angles; intercoxal piece narrow. The elytra red, with well defined widely separated punctures, sides par- allel, vestiture very short and sparse, apices transversely truncate, slightly dehiscent. The metepisternum is broad, sides parallel, outer side margined. The legs are black, hind tibial spurs of medium length. The abdominal segments have sericeous vestiture on posterior margins. Length 13 mm. Type, a male, in the Canadian National Collection; one Paratype in the collection of Mr. Wenzell. The type was collected in Cochise Co., Ariz., August 12, 1908, the paratype from the Jemez Mts., N. M. The prothorax is of the I. sanguinea type. The only near approach in color is L. ignita Sch., a very distinct species. While this description was in manuscript Mr. H. W. Wenzel of Philadel- phia sent me for examination 2 specimens of this genus from Jemez Mountains of New Mexico, one of which seems unquestionably to be a male of Col. Casey’s Leptura haldemanni, and the other a smaller female (10 mm.) of the above described L. lucifera. As both specimens were caught at the same time and place, one a male and one a female there is a suggestion that 1. lucifera may be the female of L.. haldemanni; but aside from the entirely different color which occurs in other species like 1. laetifica the punctation of the elytra is so utterly diff- ent that I have decided to let this species stand until we can prove it is or is not the other sex. Mr. Wenzel’s specimen from New Mexico seems identical except for size and I have made it a paratype. Anthophilax liebecki n. sp. Robust, entirely black except the rufous elytra with apices black. The head has moderate shallow punctures, and is strongly constricted immediately behind the eyes; the eyes large, distinctly, strongly emarginate, head not sulcate as in some species, antennae filiform, segments I to 4 piceous, 5 to LI griseous. The thorax is strongly angulate, constricted and strongly margined anter- iorly and posteriorly, punctures coarse, pronotum sulcate. The elytra are rufous, sparsely, distinctly punctured with sparse golden vestiture ; apices black, truncate. Male type. Stouter, pronotum with lateral, median, obtuse tubercle, female, dnd bits, I __ species were observed as many as thirty or forty to the square yard in young al- ~~ falfa fields and also in fall sown:rye. gs ~ Such an infestation occurred in a young alfalfa field near St. Joseph, Michi- 4 - gan, and at the time observed, October 3, practically every leaf had been stripped from the young plants. The bare stems remaining caused the field to look at ~ first glance like a clean stubble field. As the injured plants attempted to put ; out new leaves, half a dozen hungry worms were found waiting to devour each new bud. At least 99 per cent. of these larvae were of this species, there being an occasional fall army worm (Laphygma frugiperda Sm. & Abb.) and rarely a __yelyety specimen of the cotton cut worm (Prodenia ornithogalli Guen.) alle Control—One batch of poison bran mash made up of 25 lbs. of bran, 34 Ib. _ Paris green, 2 quarts molasses and about 3 gallons of water was mixed and ap- plied to 5 acres, the remainder of the field being used for a check. The mash was scattered at noon of October 3 and the early afternoon was clear though cool. At 5 o'clock it began to rain, rained all night and was raining at IT a.m. on the 4th when the experiment was first examined. At this time on the treated area, practically every worm, regardless of the rain, was lying either curled or ex- as tended on the ground and 75 per cent. of them were dead. On the check plot not a single worm was on the ground. All of them were crawling about on the alfalfa stems either in search of food or most probably to keep out of the water on the ground caused by the falling rain. : This cool rainy period was followed by warm sunshiny weather and the ~ larvae which survived the first treatment, even though a small per cent. of the extremely heavy original infestation, were able to threaten some damage to cer- tain portions of the field. Therefore, a week after the first treatment, it was ~~ decided to treat some portions of the field a second time, including that portion 2 : = Bras _ : ES = ¢* —— Fi > RLS - *Published by permission of the Secretary of Agriculture. {5 control of the corn ear worm in young alfalfa can be very likely secured by a ne Se St MI ae eg s See geo ~*~ a aoe ‘ a 72 THE CANADIAN ENTOMOLOGIST 3: met with the same fate as the first: a continuous rain having set in the eve of the day the poison was applied. However, the results were very good in and comparatively few worms survived the second treatment - Conclusion—Immediately after the second treatment the young alfalfa pla began putting out new buds and later growth enabled them to go into winter fair shape. Larvae which were taken to be H. obsoleta and L. frugiperda ¥ reared and the adults thus obtained were later determined by Dr. Dyar as the respective species to which they had been assigned. : Considering the unexpected and extremely unfavorable conditions of experiments, the success of the control obtained is rather remarkable. Good sults were obtained under very adverse conditions and given a fair chas single thorough application of poison bran mash. ae . NEW COLEOPTERA, X. BY H.C. FALL, Tyngsboro, Mass. Among a number of species of Coleoptera recently collected at Baldt Manitoba, by Mr. Norman Criddle and sent me for identification, occurred the following: Bembidion scudderi Hawyd, B henshawi Hawyd., B. salinarium SY +5 Tachys vittiger Lec., and Anthicus californicus Laf. The fact 1s mentior to call attention to the very considerable extension of the known range of the species. This is most notable in the case of 7. vittiger, which has hitherto been” recorded only from the Pacific Coast line; I have however specimens from the Salton Sea in the Colorado Desert of California. All the other species men- tioned above are known to frequent the alkaline flats of the Salt Lake region i n Utah, and their occurrence in Manitoba is at once a commentary on the physi- cal character of the country where they were found. Mr. Criddle has since in- formed me that they were taken on the shore of a large alkaline pond. Be Two other species of Bembidion taken by Mr. Criddle on the shores of this same pond will probably prove to be partial if not peculiar to such situat ne ions. One of these considerably resembles, and is evidently allied to, B. con= strictuim Say, so common along the Atlantic sea coast, and may be Casey’s socia le or particeps, though not conforming entirely to the description of either. ( other appears to be an undescribed species belonging to the small tripunctate” group, and allied rather closely to henshawi, with which it may be compa ed as follows. 3 a Bembidion obtusidens n. sp. a Color precisely as in henshawi, viz., head and thorax black with distinet green bronze lustre; elytra pale testaceous, each with a small dot or fuscous spot in the position of the first and third dorsal punctures, and between thea mn a larger transverse spot more or less lunate or semicircular in form; body be- fs neath black, slightly greenish, legs rufotestaceous. The size is larger and the form notably broader and less parallel than in henshawi; the thorax is ; Be a . ee eg: pete: j | Sait mee pte eSuaae ; : eee se ‘THE CANADIAN ENTOMOLOGIST | 171 oy e > lar n reaping, AC a little more transverse; the elytra relatively broader, more shining than is the rule in henshawi, though with a detectable aluta- ‘sculpture. In henshawi the mentum tooth is triangular, in the present cies broadly arcuate or arcuato-truncate. Length 5 to 6 mm., width, 2.05 . “The ae is a male collected by Mr. Norman Criddle at Baldur, Mani- I have also examples from Aweme, Manitoba; Laramie, Wyoming; Lagoon, Utah. It seems not to have been noticed that the name Bembidion grandiceps _Haywd., covers two quite different forms. These are both present in the Le Conte and Horn collections, and though not recognized as such by Hayward, elieve them to be specifically distinct. In the true grandiceps the head and oe ax are larger and relatively wider, and the posteriorly oblique sides of the < almost attain the angles, the latter being scarcely right, with the sides ore them subparallel for an extremely short distance. The type, as indicat- by Hayward, is in the Horn collection, and Dr. Skinner writes me that it rs the state label “Tex.,’ with the name label in Hayward’s hand. In the — Conte collection there are two “Tex.” specimens, and a third, the one on i label, bears a yellow locality disk, indicating that it was taken in the cen- : 1 Mississippi Valley (Illinois?). In my own collection are two examples om eae Kansas. . The other form may be described in a few words as follows. | 2 Bembidion rolandi n. sp. _ Similar in nearly all respects to grandiceps, but distinguished at once aoe the relatively smaller and more elongate head and thorax, the sides of the BS ter straight, and parallel at the hind angles for a distance greater than one- th | the entire basal width, the auigles ye rectangular or ae nearly iF Bembidion semiaureum n. sp. on This name is proposed for a very large form of the fuscicrus type which — stood for years in my collection awaiting in vain the possible advent of in- te nediates which might connect it with the latter species. The color is nearly — fuscicrus, viz—head and thorax greenish black, polished; elytra testa- us with an oval fuscous discal spot which begins at the anterior dorsal punc- a and extends somewhat to the rear of the posterior puncture; it is limited’ ly at the fifth stria, and continued to base by a rather broad parallel sut- — - : | stripe, which involves the first two interspaces. There is no indication oft as ae eral extension of the fuscous spot, as is frequently the case in fuscicrus. — a body beneath is black, legs entirely rufotestaceous. The prothorax is ey : less narrowed behind than in fuscicrus, the base being only just Dems Ces bly narrower than the apex. Length 6.2 to 7 mm. 0 boldt Co., California Ea ae gysia he ws tee a Peri teat se = bee og oS ny RO ee ET nce cana : eg OO ae Sea ty ean: . “¢ 2S se pote “aly 7 — “y pO . ~~» s 1a 172 ‘ THE CANADIAN ENTOMOLOGIST - Fuscicrus is a conspicuously smaller and somewhat narrower | rarely much exceeding 5 mm. in length, the thorax smaller and more nar ed laterally, even in some cases to the side margins; the hind femora 0 more or less piceous. Specimens in my collection from Ft. Yukon and ~ part, Alaska, are undoubtedly Mannerheim’s lucidum var. b.,” to which schulsky gave the name fuscicrus, and are, moreover, quite inseparable ire Wyoming and Colorado specimens at hand, to which the names caducum, al- eae | and perhaps GEES of Casey’s recent Revision are applicable. Pe: Rae toba by Mr. Criddle and Mr. Wallis, one of anes was taken at Baldur « Or shores of the alkaline pond already referred to. ‘These may be described follows. Dyschirius interior n. sp. se Closely allied to the Californian tridentatus Lec., with wien it: must st b associated because of the wide elytra margined at base, and the clypeus trid tate. The form is very distinctly narrower than in tridentatus, the legs” rufc instead of nearly black, and the prothorax, elytral apex and body beneath sh a more or less marked rufescence, the general color, however, being black y green bronze lustre. The front is transversely sulcate, the frontal crest wanting. The third elytral interspace is tripunctate, all three punctures ly near the third stria. The apical protibial process is here a little longer than t terminal spur, while in tridentatus the reverse condition seems to prev Length 3.7 to 3.8 mm. : Four examples have been seen, all taken at Baldur, Manitoba by Mes Norman Criddle, J. B. Wallis, and L. W. Roberts. Aside from tridentatus, the only other species in our fauna having base of the elytra margined, the clypeus tridentate, and the third elytral inti tripunctate, is the Californian varidens Fall, a considerably smaller speci to 3 mm.) with more finely striate elytra. : Dyschirius perversus n. sp. Elongate, parallel, thorax nearly as long as wide, feebly narrowed | front and scarcely perceptibly narrower than the elytra; color black with g bronze lustre, legs rufous. Front transversely impressed; elytral striae enti finely but distinctly impressed except at the extreme base; striae moderat punctate; third interspace bipunctate, the first puncture near the base and ° ally on the third stria, the other near the third stria at about the apical fife Front tibae subedentate externally. Length 4.8 mm; width 1.3 mm. Described from a single exampie submitted = Mr. J: B. Wallis cet label, Miami, Manitoba, 16—VI—17. % y Le Conte’s table (Bull. Brook. Ent. Soc: 1879) this species falls 4 phidsericollis and edentulus. Sphaericollis is larger, with a more transverse t ax and generally stouter form, and in it, as in its associates, it is the basal pu 1 ture of the third interspace that is lacking rather than the intermediate _ Edentulus is, 1 think, unknown to American students; at- any rate i large size—7 mm.—is sufficient to exclude it. ee ~ nat: me SEL Sk ahs =r z 5 - » aoe Secs i re : _ Listrochelus longiclavus n. sp. eee, Rather stout, oblong oval, a little broader behind, entirely rufotesta- _ the head and thorax with sparse erect hairs, elytra glabrous. Head sely punctate, the clypeus less densely so; clypeal margin broadly reflexed, jato-truncate, the angles rounded. Prothorax three-fifths as long as wide, s nearly straight and parallel in basal two thirds, thence strongly converg- t to apex, side margins barely perceptibly crenulate; surface uniformly punct- e, the punctures distant on an average by their own diameters. Elytra htly rugose and rather closely punctate. Length 11.3 to 12.3 mm. ~ Male— Antennal club very elongate, nearly twice as long as the stem; ntral surface flattened, the sixth segment and the median parts oi the fifth except at base, closely punctate; tarsi very slender, much longer than tie tibiae, laws all similar, slender, with a small acute tooth at about the basal two-fifths. ntire inner edge of the claws is at first sight apparently unmodified, but inder sufficient power is seen to be uniformly minutely pectinato-serrulate. fo Described from two males from Eagle Pass, Texas, submitted by Mr. ren Knaus. Type in the writer’s collection, paratype in that of Mr. Knaus. x: This species resembles in a general way L. flavipennis, but is of some- -stouter form. The very long antennal club combined with the structure ¢ he claws will distinguish it from any hitherto described species. The free angle e of the hind coxae is not at all produced. 2 ee _ Macrobasis subglabra n. sp. Form slender; entirely black; subglabrous; head and thorax sparsely punctate, elytra finely rugose, but not distinctly punctate. Head not ened toward the vertex; prothorax subquadrate with oblique front angles, im with fine, feebly impressed median line. Antenae nearly as in unicolor, st joint not quite as long as the three following. Protibiae of male wn two Sp ars. Length 7 to 10 mm. Described from a series of ten specimens taken by Mr. F. S. Carr at lt Secon. Alberta, and a single example from Redvers, Saskatchewan, sub- ed by Mr. C. A. Frost. The type is an Edmonton male bearing date “q— 39 : _ This species is closely allied to wnicolor, and with insufficient material it be ee of being small, denuded ere of the latter. Mr. Carr Fe tear the margins. In unicolor the head is a little widened tow aa the ver- and therefore less quadrate than in the present species, the pubescence al- distinct and dense enough to give a grayish aspect, the size averaging 1 ally larger. The Le Conte collection contains two examples of this species from the Red River, placed with unicolor. ee sk: ; ee The an of all the above described peel are contained in the author's : Were tee Mie ha ok Saat S aeE oe a “ : Sepa ea oS," tant 174 - cess THE CANADIAN ENTOMOLOGIST =~ ae . s pire LIST OF NATURAL ENEMIES OF THE CELERY LEAF-TYER (PHLYCTAENIA RUBIGALIS GUEN).1 (oe BY F. H. CHITTENDEN, U. S. Bureau of Entomology, Washington, D. C. of these in one short paper, especially in view of the fact that at the time t the author’s first paper on this leaf-tyer was published in Bulletin 27, Da Entomology, in 1893, only a single enemy was known. All of the species Y are here listed are parasites. os Synetaeris sp.—This ichneumonid was identified with its host in at Livonia, Pa. (Identification by Dr. Ashmead). : Pimplidea sanguineipes Cress——This species was reared from the green-_ | house leaf-tyer, February 15, 1916, by Mr. B. L. Boyden, Oxnard, Calif. (Det mination by Mr. Cushman). Rogas rufocoxalis Gahan—Reared in November 11, 1918, Alhambra, cal ne by Mr. R. E. Campbell. (Identified by Mr. A. B. Gahan). ; Campoplex (Omorgus) phthorimaeae Cush—Reared by Mr. Boydeds a Calif., October 18, 1915. (Identified by Mr. A. B. Gahan). Microgaster congregatiformis Vier—Reared by Mr. aa at Oxnard, Calif., October 18, 1915. (Identified by Mr. A. B. Gahan). Amorphota infesta Cress—This ichneumonid fly (Chttn. No. 140802) was raised from its host February 10, 1909, from material collected by Mess rs. McMillan and Marsh at Smeltzer, Cal. (Determination by Mr. Viereck).— Meloborus sp—Reared from its host from material collected by Mes a Marsh, September 18, 1908, at Oxnard, Calif. (Determination by Mr. Viereck ) Ar Chalcidid—An imperfect specimen of a chalcidid, reared by Mr. Boyd en at Oxnard, Calif., February 10, 1916, not determined. Tetrastichine (?)—-A secondary parasite, bred on Microgaster congre- gatiformis Vier. as host by Mr. Boyden, Oxnard, Calif., February 15, 1916. (Identification by Mr. A. B. Gahan). Trichogramma minutum Riley —Reared by Mr. Boyden at Oxnard, ‘ ut March 14, 1916, as egg parasite. (Identified by Mr. A. A. Girault), ws oy seu Syntomosphyrum modestus Houd.—An egg parasite raised: by Mr. Boyder at Oxnard, Calif., March 14, 1916. (Identified by Mr. A. A. ae é . Dibrachys boa hate Ratz.—Reared by Mr. Boyden at Oxnariss February 10, 1916. (Identified by Mr. A. B. Gahan). 1—The American species, according to Mr. Carl Heinrich must be known by this ni ferrugalis Hbn., not occurring on this continent. y , les i ae Re ® ox) reprrasscam waste foe “THE CANADIAN ENTOMOLOGIST 175 lant thrsp. ’ / : ’ § ; ~~ abgngy Pom int w = Ss ESS SS g — v/ ‘ ‘ if / Mh PROTHORACIC GLAND OF RED-HUMPED APPLE CATERPILLAR. "es . TE eS, FE SMES av NEL? Cnr tpg Ot aR a ee 2. eee 3 x PP ES - : pnmtes 2 ¥ Ewe ES << ‘ - . < tS aes f : ie eee 176 THE CANADIAN ENTOMOLOGIST. = . : is eee THE VENTRAL PROTHORACIC GLAND OF THE RED-HUMPED APPLE CATERPILLAR! (SCHIZURA CONCINNA SMITH & ABBOT). — BY J. D. DETWILER, Western einer London, Ont. of ejecting a fluid no its foie A few experiments were Abate and the phe- Z nomenon presented such interesting phases that a somewhat detailed study of its general features was decided upon. Nature and Source of Secretion. The first experiment with the larva was a determination of the secretion’s reaction towards litmus. A caterpillar was placed on strips of both red and blue litmus paper and mechanically irritated. A sudden reddening ot the blue paper then took place showing plainly that the secretion was acidic. The ejec- — tion of the liquid was almost instantaneous, and being unacquainted with glands — 4 of this nature its source was not detected. An examination of the caterpillar’s a body revealed many small drops of liquid on its surface, suggesting as the source : numerous hypodermal glands. A small sheet of blue litmus paper, was then a notched and fitted over the caterpillar’s-body in the form of a yoke, so as to a: isolate or partition, one part of the body from the other. On irritating the cater- _— pillar the paper was again reddened by the spray, but the body behind the paper — partition remained dry. In this way the cephalic location of the gland was ae: 3 33 termined for, by close observation, after sufficiently disturbing the caterpillar, ~ a fine spray of a clear liquid could be seen issuing from the ventro-cephalic | ao region of the thorax. The odour of this secretion is very similar to that of 5 “3 vinegar and sufficiently strong to irritate the nasal passages. Historical Sketch of Earlier Observations. Comparatively few entomologists have noticed the occurrence of the secretion in this species, and only one localized its source. The earliest record was made by Saunders of Canada, who in 1881 reported 2 that when the larvae were handled they discharged from their bodies a trans- — parent fluid of a strong acid odour. Six years later Denham observed that older — larvae “ had the power to emit quite a quantity of strong hydrochloric acid mee strong enough to be decidedly corrosive to the skin and easily perceptible in a the atmosphere.” In 1895 Packard stated that while examining the very gaily ae colored and highly spined caterpillars, he observed that when a fully grown a né e . was roughly seized with the forceps or fingers it sent out a shower of spray from each side of the prothoracic segment exactly like that of Cerura (Harp i vinula. In this article he also definitely credits himself with the discovery of # gland in this species. Foster in 1902 also noticed the secretion and described > <> 1—A preliminary paper was published in the Annals, Ent. Soc. Amer. (1919) in ‘con- junction with Professor Herrick and entitled, “Notes on the Repugatorial- Gh nds_ of Certain Notodontid Caterpillars.” : THE CANADIAN ENTOMOLOGIST L7F as a transparent watery fluid with the odour of sulphuric acid, and further that it exuded from the caterpillar’s body wherever it was touched. So far no records have been found where the gland was actually observed. Range and Ejection of Spray. The result of the litmus paper test suggested a very promising method of. detecting the extent to which the liquid could be ejected. Large sheets of blue paper were fastened together covering in all a space of about eighteen by twenty- two inches. A caterpillar was then placed in the centre and irritated. Directly a graphic representation of the extent of the spray was registered for the strong acid readily reddened the blue paper?. In this way it was found that the cater- pillar could spray a considerable area at one operation, and that it appeared to have some directing sense and power. The most normal action, however, seems to be that of sending the spray backward over its body,—a natural direction since it is here that it is most likely to be attacked. Some idea ot the area covered may be formed from the fact that a caterpillar has been observed by the writer to send the jet a distance of eight inches and also that the spray tends to spread out very considerably. The act of ejecting the liquid is quite characteristic and gives the caterpillar a somewhat formidable appearance. When strong mechani- cal irritation is applied,, for example, the head is thrown up, jerked to one side and a jet of clear liquid emitted through a small tongue-like organ momentarily protruded from the mid-ventral region of the neck. The ejection of fluid is almost instantaneous, resembling very much the emptying of a pipette when the rubber bulb is suddenly and forcibly squeezed. General Form and Location of Gland. The gland consists essentially of two divisions arranged in tandem and con- nected by a short tube. The anterior part is bulbous and relatively small, while the posterior one is sack-like and large® (fig. 1). The anterior and apical part of the bulb is connected by a short “false duct’ to the external opening which is located in a ventro-medial position just behind the anterior margin of thé pro- thoracic segment. The sack extends backward to the posterior border of the metathorax and rests to a large extent on the flattened anterior portion of the much enlarged mid-intestine. It will thus be seen that the whole organ passes. somewhat diagonally through the entire length of the thorax and also that it occupies the major part of the space in this region of the body. | Position of Gland in Relation to Other Organs. Normally, in insect anatomy, one finds that the oesophagus, after coming up through the nerve collar, passes backward in a medial direction to the mid- intestine. In this case, however, it is pushed to one side, usually to the left to make room for the gland which also arises in the middle line. This displacement 2—The article referred to in the previous foot-note describes a series of experiments subsequently carried out by this method and also a diagram of the actual range of the spray. 3—For convenience these two divisions will be referred to as "bulb” jand “sack” res- pectively, it being understood that the terms are not necessarily significant of their functions. THE CANADIAN ENTOMOLOGIST oa iv,<} 17 may be so great as to radically change the symmetry of the intestinal tract here, causing the fore-intestine to connect with the mid-intestine considerably to one side (fig. 2.). In fact the junction has been observed to be so far to the left that the fore-intestine was quite in line with the left half of the mid-in- testine. ; The silk glands also suffer considerable displacement. Normally, one would expect to find them on their respective sides of the body since their ducts do not connect until they have passed the gland in front. But in S. concinna this is not their usual position, for both appear, as a rule, on the left side, their ducts passing forward on the same side until the vicinity of the bulb has been reached. This condition, however, may be reversed. When they are both on the same side the duct of the displaced gland in passing over to its proper side, before uniting with its fellow to form the single duct in front, usually keeps character- istically clear of the bulb (figs. 2 and 3). In only two instances has this duct been noticed passing across the front of the bulb. In one of these instances the glands were both on their respective sides of the body but the duct of the right gland on reaching the bulb passed to.the left of it and then back again to the right side across the front of the bulb. Even the nervous system may be forced to-deviate from its mid-ventral course or even td modify its symmetry. In the first place the bulb, as it comes up from beneath the suboesophageal ganglion, tends to push the connectives to one side*, almost invariably to the left® (fig. 2), and secondly, the prothoracic ganglion itself may be considerably distorted, its apex turned toward the left, due to the medial position of the bulb (fig. 4). One can readily understand why the oesophagus, and to some extent also the nervous system, should give way to such a large organ tending to occupy the same position. It is difficult, however, to understand the shifting of the silk glands to the same side, thus necessitating a circuitous course of the duct in order to return to its normal position. Possibly a study of the development of the larva would explain this. From the varied positions that this gland may occupy with respect to the other organs, it appears to have reached an abnormal degree of development in this species. Tracheation. The whole gland receives its oxygen supply from the anterior pair of thor- acic spiracles. Two rather prominent branches, one from each side, issue from the mass of tracheae here and pass inward to the sack. On reaching it one branch goes to the dorsal surface and subdivides there while the other passes to the ventral half. On the principle of bilateral symmetry one would expect each branch to supply its respective lateral half. Almost invariably, however, the branch from the right side goes to the upper surface and the left one to the lower (figs. 2 and 3). In only one instance has this condition been found to = be reversed. ‘These two main branches may also contribute to the tracheal sup- ply of the upper part of the bulb (fig. 8). 4—Dimmock, A. K. 1882, noticed a similar displacement in thie cords of Harpyia vinula (an European species) and stated that it is more pronounced in ithe earlier stages. I have not investigated this phase of the problem in S. concinna. £ 5.--As I recall, there was one instance where the cords passed the gland on the right. A THE CANADIAN ENTOMOLOGIST 179 Boe VG. LTV; PLATE 4. 180 THE CANADIAN ENTOMOLOGIST The bulb receives its main supply from two pairs of branches, one pair going to the dorsal® surface and the other to the ventral. The former pair is somewhat interesting from the fact that it forms a continuous circuit across the dorsal surface of the bulb, making a broad loop here from which it sends off branches. In this way a continuous trachea passes from one side of the thorax — to the other (fig. 2 d. bu. tr.). In some larvae the middle part of the loop is weak- ened and the branches come off in two main groups, but this grouping may also occur where there is no weakening of the loop (fig. 2). This condition is prob- ably reminiscent of a time when each branch supplied its own side independently. The pair going to the ventral surface does not make a medial connection but each branch keeps to its own half, where it divides and subdivides normally (fig. 8). . From this it will be seen that each division of the gland is well supplied with tracheae, a provision quite significant when the function of each is con-~ sidered. The tracheae also, very probably, perform a partial suspensorial func- tion, there being no muscular attachment over the whole gland except at its anterior extremity. This accessory function may, in fact, have given rise to the — continuous loop over the dorsal wall of the bulb. As to the peculiar disposition — of the tracheae going to the sack, in which one branch or trunk supplies the dor- sal half and the other the ventral, it seems reasonable to suppose that each does normally supply its own lateral half but that as a result of an extraordinary development of the gland, the sack has turned or fallen over to one side, the direction being almost invariably to the left. In fact this turning does not appear to have been quite complete, for the plane dividing the tracheated halves is not perfectly horizontal but inclines a little to one side, that is, to the mf right (fig. 3), showing that the leftward orientation is imperfect; nor does the direction of falling appear to be permanently established for, as noted above, the usual disposition of the right and left tracheal branches over the sack may 3 be reversed. This theory of turning, due to extraordinary development, can, no a doubt, be checked up by embryological studies, or perhaps even by examining pa the early-stage larvae. In support of the theory it might be stated that the writer has discovered homologous glands in a few species of the genus Datana, also Notodontids, in which the structures were so small that the elasticity of their own tissues would no doubt hold them in place. ‘Their tracheation has, however, not been studied’. 6—Although the bulb naturally stands more or less erect it will ‘be considered, for de- scriptive convenience, as lying on the ventral body-wall and the antero-dorsal surface will be referred to as the dorsal surface. A similar consideration will — apply to the other aspects of the bulb. as 7—In dissecting a number of Datanas (D. ministra, D. contracta, D. integerrima and D. angusii) I found that they too possessed glands somewhat similar to that of S. concinna, but evidently very much simpler in structure. In testing the con-- tents of the gland of D. integerrima it also was found to be acidic. I might here add that I also experimented with Sciizura unicornis and found that it secreted an acid fluid and that the operation of the gland is practically the same. as that of 9S. concinna. I have found no other record of ventral prothoracic — glands in these species. — ea ae ee eee a THE CANADIAN ENTOMOLOGIST 181 Musculature. The musculature of the gland is somewhat remarkable in that it is wholly situated at its anterior end. As the individual muscles are small and close to- gether, they can be studied best by pulling the gland backward so as to stretch this area, thus separating the muscles more or less’. When this is done they will be seen to be arranged in pairs (a muscle on one side having its correspond- ing muscle on the other) along the lateral margin of the organ beginning at the extreme cephalic end of the “false duct’ and extending back a short distance beyond the apex of the bulb (fig. 6). At the extreme cephalic end of the “false duct” and just inside of the ventral body wall, there will be seen three pairs of muscles (fig. 6, a, b, c,) radiating from the ends of ‘the transverse slit which constitutes the external opening. The anterior pair extends to the caudal mar- gin of the head while the other two pairs pass laterad to the body-wall being at- tached close to the first pair of thoracic spiracles (fig. 11), one in front and the other below. Close to these muscles and appearing almost as lateral exten- sions of the duct is another pair (fig. 6, d). These are short and have their origin in the body-wall at a point about half way between the duct and the an- terior spiracles. A short distance behind these and still in alignment with the lateral margin of the duct the fifth pair is inserted (fig. 6. e); these also extend to the body-wall, their origin being below and close to the spiracles just men- tioned. From the point of insertion of each of these last mentioned muscles there arises a very slender muscle (fig. 6, f), the pair passing upward and out- ward to their origin on the caudal margin of the head. Accompanying this pair of muscles are three other pairs inserted one behind the other along the lateral margin of the apex of the bulb (fig. 6, g, h, i) and originating in the ‘same area as the slender ones just mentioned. One pair still remains to be de- scribed (fig. 6, elb. mus.). They are characteristically elbowed and can be seen to good advantage when the gland is thrown forward. They will then appear as two miniature columns passing upward from the ventral body-wall, just be- hind and a little to each side of the apex of the bulb, and attached directly be- low the insertion of the most posterior of the three pairs of muscles just described. A short-distance from their insertion they make a sharp bend (elbow) and pass downward to their origin close to and behind the posterior margin of the external opening. From this point they pass backward in their attachment along the body-wall to the ridge separating the first and second thoracic seg- ments. They also appear to be more or less continuous with other ventral body-muscles. Froni the ventral position of these muscles it will be seen that they must be capable of relatively great extension when the head is thrown upward and the apex of bulb is forced forward, ‘heir elbowed con- dition is then evidently nature’s most convenient way of accommodating their length to the short space resulting when the caterpillar is undisturbed. Morphology. As mentioned before, the gland proper consists of two distinct divisions, one bulbous and the other saccular. The former is more or less pear-shaped 8—It will be necessary to first dissect away the mass of body muscles and tracheae that occupy this region of the thorax. 182 THE CANADIAN ENTOMOLOGIST and distinctly bilobed at its larger end. This is due to two well defined lateral furrows, one on each side, which externally divide this structure into dorsal and ventral halves. ‘These furrows not only traverse the whole length of the bulb, but also that of the short tube connecting the two divisions (fig. 7). The narrow apical end of the bulb widens somewhat laterally, and its walls show a dorsal and ventral pair of darkened areas, which are evidently heavily chit- inized points for attachment of the muscles which were found inserted in this. region (fig. 6, chi. pt.). The lumen of the bulb here also shows the lateral wid- ening, the whole space ending rather abruptly, due to the truncated terminus. of the bulb. In this somewhat abrupt terminal wall can be seen the true open- ing of the glands which consists in a transverse slit with whitened lips. It is called the “true” opening since it is this part of the gland that is protruded through the body-wall opening:when the liquid is ejected. When thus protrud- ed, two small, finger-like projections arise from the lateral angles of the an- terior margin of the apex (figs. Io and 11). ‘These fold towards each other when the apex is withdrawn. On the ventral side of the apex is a small, median lump-like structure (figs. 8 and 18, s-ap. lmp.), which is white in color and by transmitted light appears to be hollow. Its white color contrasts rather strong- ly with the distinct yellow of the bulb. - Connecting the end of the bulb with the external opening is a short tube, — which has been referred to as a “false duct,” and which is really an infolding of the body-wall. ‘This invagination of the body-wall evaginates when the apex of the bulb is forced out through the external opening. It is thus seen that the gland itself is not evaginable, but only the false duct. The anterior end of the false duct terminates with the more or less chitinized lips of the external opening. ‘The anterior lip of this opening appears as a rather loose fold while the posterior one is thinner and discloses a small chamber when drawn back sO as to separate the lips. The form of the saccular division is best described by the name given, for it looks indeed like a sack. It is somewhat oblong, evidently favouring an ovoidal shape with the larger end nearer the bulb. Its shape, size and very white color, contrast strongly with the bulb. ~ : _ Dimensions. - In order to form a more concrete idea of the size and relative proportions of the gland, a few of the more important dimensions will be given. In the ~ dissections only final stage larvae were taken, and even here the measure- ments vary much, for during the instar very considerable growth takes place. In one dissection, the dimensions were as follows: total length of gland 6.5mm., length of sack 4.33 mm., width of sack 3.6 mn, and length of bulb 2.17 mm.® This was the largest gland of which a measurement was taken. In another dissection, the total gland in situ, occupied a space of 4.5 mm. in length. The ~ apical end of the bulb narrows decidedly. Some idea of its size may be torm- ed from measurements made of the part when extruded. In two caterpillars ee = = ~ ST 9—Computed from drawing made to scale. In this case tthe connecting tube was concealed by the dorsal lobe of the bulb and hence no measurement is given for it, » s ai pee ane . interest in the problem as a whole. The writer also wishes to express his grati- . tude for helpful suggestions given by members of the Entomological staff. a LITERATURE CITED Berlese, A. 1909. Gli Insetti Vol. I. pp. 529-531. ae Denham, Chas. S. 1888. The acid secretion of Notodonta concinna, Insect aoa E: PS Vol. 4, p. 143. : Dimmock, Anna K. 1882. Asymmetry of the Nervous System in the Larva of Harpyia, Psyche, Vol. 3, pp. 340-341. Dimmock, Geo. 1882. On Some Glands which Open Externally in Insects, Psyche, Vol. 3, p. 391. a 13—For a general discussion of these glands see Dimmock (1882), Piackared (1890) wae Latter (1887). These authors also give references to literature while Packard (1896) devotes a paper entirely to literature on eversible glands. A very ex- — cellent study of the secretion of C. vinula is given by Poulton (1887), the £Be ¢ os having been well described by Klemensiewicz (1882). See also Berlese (1909). - 35 = ina &, ‘a ae 13, p. 293. Pp. 44-48. Be * 32, pp. 408-474. _ Latter, O. H. 1897. The Prothoracic Gland of Dicranura vinula, and other es _ Notes, Trans. London Ent. Soc., pp 113-126. Pe Packard, A. S. 1895. The Eversible Repugnatorial Scent Glands of Insects, ~~ Jour. N. Y. Ent. Soc., Vol 3, pp. 110-129. 6: Gee 'ackard, A. §. 1890. Notes on Some Points in the External Structure and ¥. : _ Phylogeny of Lepidopterous Larvae, Proc. Boston Soc. Nat. Hist., Vol. eee. 25, pp. 94-97. ei Ss >= sects, Jour. N. Y. Ent. Soc., Vol. 4, pp. 26-33. we Poulton, E. B. 1886. Notes in 1885 upon Lepidopterous Larvae and Pupae, ~~ ete. ‘Trans. Ent. Soc., London, pp. 156-160. Fs Patten, E. B. 1887. The Secretion of Pure Formic Acid by Lepidopterous — "oh * _ Larvae for the Purpose of Defense, Report Brit. Assoc. for the Advance of Se., pp. 765-767. - < Ges are Rost gion of) > ahd oe * oo = t? Neer A Gemma er a ke Oe MR ect IN eS yg ae Le: os oe > ; ‘ ‘ “You apo . NA SS . 3 2 ~ . 2 ae yh seg ee Bie i ane wt le tn i - a = =" Gus?” eat Be ~ eta et THE CANADIAN ENTOMOLOGIST 189 Ey HL 1902. Note on Larva of Schizura concinna, Ent. News, Vol. | 5. E Herrick, G-W. and Detwiler, J. D. 1919. Notes on the Repugnatorial Glands — ee of Certain Notodontid Caterpillars, Ann. Ent. Soc. of Amer., Vol. 12. Ie icccicice S$. 1882. Zur naheren Kenntniss der Hauptdrusen bei den Raupen 4 und bei Malachius. Verhandlungen d. Zool.-Bot. Gesells. Wien, bd. — HE Packard, A. S. 1896. Literature on Defensive or eahikaactiat: Glands in In. = unders, W. 1881. The Red-humped Apple Tree Caterpillar (Notodonta con-_ cinna), Can. Entomologist Vol. 13, p. 139. ABBREVIATIONS . ~ eae a, b,c, d, e, f, g, h, i, .... see text under “Musculature” Aun e- TE ale en ee ea first abdominal ganglior ie GR nh a a eee apex ¥ ay Sy CRY ee eens ore brain ets Dees oe oe LE Ty bulb of gland << Sele AGRE we Loa hs So Lehn basement membrane me es eerear-tne Se bate Oe, trachea to dorsum of sack ge | 2 Et pe ee eyes mene Mi SM Sent os 2. 2G ol elbowed muscle ie SS Sey ener -.... fore-intestine Perris ee aes P25 SL. false duct eS SS soe Shs Be head . OTE) Ah in Saree come intima ; oe ES ee left anterior thoracic spiracle (re- . is teres aos ca Se Seat ees per ~ 190 THE CANADIAN ENTOMOLOGIST bece > ‘Ch aie 3 ital Bees serait err et te lateral furrow WEP IEEE.* ¢ 3 Go eta. ie eh mid-intestine HPPONE hace see eee mid-intestinal trachea SES Peete oe ak ee eee nucleus ; ICTS SY She ee ess hae a oe nervous system pesdik sms: 4% be Sees posterior dilator muscle Gants thr ssp: 2 cess . right anterior thoracic spiracle (region of except in figure 10) Semis Ling tea Soe Pn ag eee sack of gland Ras ee nid RAs Migr et silk duct Te, 2 Soe eee Pie ee Rar fete ats silk gland Bar hed Se Pen, Ge oes stellate cell Sipitip pene ons 5 ect sub-apical lump SOG SON a fae raw tees suboesophageal ganglion spin., Chae SL, Da See Spiess Pe spinneret thr. ong. EAs te cs pepe enon tae prothoracic ganglion thr. gng. 2, ........+... mesothoracic ganglion PRAT Vos ek ee oie metathoracic ganglion ‘AR pee ia Seen are iy sie hatPay ea - trachea PSA TER tA tae Ngee eae trachea to venter of bulb Mecca ieee fees Os trachea to venter of sack BR hk a oe aa ae vacuole I{xPLANATION OF PLATES. Plate 3. Fig. 1. Final stage caterpillar of S. concinna in a natural feeding posture; internal organs somewhat diagrammatically illustrated; actual length about 1.25 in. F ig. 2 Dissection of organs in anterior part of Bony: dorsal an phagus Pied to left and other organs in normal Racibieass : Fig. 4. Dorsal aspect of suboesophageal, and prothoracic ganglia, and — postero-lateral view of bulb and connecting tube. ae Fig. 5. Sack turned on its right side. ats Fig. 6. Musculature, dorsal aspect, including corrugated apical end of bulb; anterior part showing muscles “a”, “b” and “c”. somewhat ing ically illustrated. : Fig. 7. Lateral aspect of bulb and connecting tube showing only corr gated lining (intima). : Fig. 8. Latero-ventral aspect of bulb, connecting tube, Howes part of sack < and sub-apical lump (gland thrown forward). : Plate 4. Fig. 9. Normal position of gland figured in number 8. Fig. 10. Ventral view of anterior part of caterpillar. ee Fig. 11. Lateral view of anterior part of caterpillar. ‘ Fig. 12. ‘Tangential section of bulb wall showing the over-lying secrete ot cells. a Fig. 13. Stellate cells, the intima removed, and the cells standing on basement membrane when drawn. : = ¥. es ooye os 308 1 oat 7 ™ as Fog, oe : pe ae & ]. No. and Sexes of Types: Holotype ¢, Allotype 2, 29 Paratypes ¢ 9. Dates of Capture: V, VII, IX. Types in: Collection of Author, and Barnes; also 1 Paratype, U. S. N. M. This insect to some extent resembles vecors, irrorata, pucrilis and when badly rubbed—furfurata, but seems abundantly distinct: The vestiture is far more scaly than is typical for members of the group Orthodes, and the satiny luster to the wings more pronounced. ‘The vestiture lis so scaly that the insect might well be placed in the genus Mamestra (Polia) were it not for its general appearance, resemblance, and apparent close relationship in all other characters to described members of the group Orthodes. Chytonix sensilis form macdonaldi form nov. Sir George Hampson places Chytonix sensilis in that group of the genus Chytonix having simple antennae in the male sex. However, the Cat. Lep. Phal., B. M.,. seems to indicate that he did not know the male, which is similar to the female in pattern and maculation, but the antennae are laminate, the laminations almost forming short pectinations. ‘Two males of the typical form were taken; and also one female without the white spot below the black streak con- necting the transverse anterior and the transverse posterior lines in the sub- median fold. This corresponds to ab. J. of Hampson. One male and two fe- males lacked the black streak, and in these the white spot is completely diffused by mixing with a suffusion of whitish scaling in the medial area. The result- ing insect scarcely resembles the typical form, and may henceforth be known a | THE CANADIAN ENTOMOLOGIST 197 under the form name macdonaldi, in remembrance of the many nights in the Pine Barrens during which Neil F. MacDonald, 5B. Chem., assisted untiringly the work of the author. The general condition of all the specimens of this form taken is none the best. The females are in better condition than the male, and hence one of these is designated the holotype. This specimen has the transverse anterior and transverse posterior lines spaced a little further apart on the inner margin than is typical of C. sensilis. The male allotype and female paratype are nor- mal in this respect. . Type Locality: Brown’s Mills in the Pines, N. J. No. and sexes of Types: Holotype 2, Allotype ¢, 1 Paratype @. Types in: Collection of Author. Olene atomaria form aridensis form nov. Size, lines and ordinary spots similar to O. atomaria. Female: fore- wing; basal area filled in with chocolate-brown to the transverse anterior line ; subterminal area similarly filled; the medial area pale, olivaceous, with tenden- cies to blueish in some specimens and greenish in others, more suffused with color basally and inwardly. This gives a general impression of O cinnamomea, but the size is larger and it matches in no other details. The reniform spot is strongly outlined with a fine chocolate-brown line. and 1s filled in paler than the pale medial area. As usual with species of this genus the basal edge of this spot is strongly marked. Hind wings an even medium brown with only the discal spot showing in some specimens, while in others a trace of a shade line is to be found. In this respect as well as in the peculiar coloration of the fore- wings, the form differs considerably from typical O. atomaria. Under side with discoidal spot, and shade line half way between spot and outer margin. Male: fore-wing with the basal area strongly tinged with purple; the subterminal area lighter brown than in the female, with a purplish and white patch on anal region; otherwise similar to the female, except that there is a waved line of the same color as the medial area through the basal brown area, thus cutting this into two parts. On the underside, the spots and lines are similar to the same ones in the female, but somewhat more suffused and broader, with the line on the fore-wing somewhat nearer to the spot. This form is described mainly at the suggestion of Dr. William Barnes. At Brown’s Mills in the Pines, N. J., atomaria runs to two forms; one much lighter than typical, more suffused, and with much less brown on the fore-wings. Of this form I have two specimens: ¢ 9, the ¢ taken 31-VIII-19, the 9 5-VIII- 19. The other form is described above. Type Locality: Brown’s Mills in the Pines, N. J. No. and sexes of Types: Holotype ?, Allotype ¢, Paratypes 112 2, also I egg from Holotype. Dates of Capture: August. Types in: Collection of Author ; 2 Paratypes and egg, Collection of Cornell University, 2 Paratypes, Collection Wm. Barnes. 198 . THE CANADIAN ENTOMOLOGIST NOTES ON FUNGOUS INSECTS. BY HARRY B. WEISS and ERDMAN WEST, ‘ New Brunswick, N. J. The following notes on fungous insects have accumulated since the publi- cation of former papers along this line.* Records not specifically credited were obtained by the writers. In Entomological News Vol. XXX, No. 5, pp. 144—5, Mr. W. H. Well- _ nouse calls attention to Mycodiplosis cerasifolia (Dip.) feeding on the spores of Crataegus rust (Gymnosporangium clavipes C. and P.). Mr. Wellhouse found . the larvae of this itonid living among the aeciospores and feeding upon them. Gravatt and Posey (Jour. Agric. Res. vol. 12, No. 7) state that “larvae of the gipsy moth (Porthetria dispar) feed on the peridermium stage of Cronartium ribicola and carry thousands of aeciospores on their bodies.” ‘They further state that the larvae feed abundantly on the spores and injure the fruiting layer of the postules so that further spore production is arrested. In a letter Mr. Thos. E. Snyder informs us that the beetle Cupes concolor is usually found in the southeastern states in oak stumps upon which are grow- ing the fruiting bodies of Daedalia quercina; the larvae of this beetle boring in the wood which has been penetrated by the mycelium of this fungus. Meyrick in his “Handbook of British Lepidoptera,’ mentions some seventeen species of Tineidae, the larvae of most of them being recorded as feeding on lichens. Perris in “Larves de coléoptéres,” Paris, 1877 (Ann. Soc. Linn. XXII, XXIII) mentions Tetratoma baudueri in Agaricus ostreatus (p. 154), Bolito- phagus armatus in Boletus suberosus (p. 116-7) and Cis living on branches in- fested by Telephora sp., (p. 65.) Ganglbauer in “Die Kafer von Mittel Europa, Ill” records Liodes cinnamomea in truffles (p. 209), Agathidium seminulum in Trichia cinnaberina (p. 241), Diphyllus lunatus Fab. in Sphaeria concentrica — (p. 654), Cryptophagus lycoperdi in puftballs (p. 675), Lathridius rugosus on slime mould (myxomycetes) (p. 786), Triphyllus bicolor Fab. in Fistulina hepa- tica (p. 825) and Lycoperdinen on Lycoperdon and Bovista species (p. 912.) The following records relate to species in this country which have been found to be Bete iy more or less with polypores and gill fungi. SLUGS ! Limax maximus L. Sometimes eats ragged holes in caps of cultivated mush- rooms. (Popenoe, U. $. D. A. Farmers’ Bull. 789.) SOWBUGS Armadillidium vulgare Lat. Greenhouse pillbug. Sometimes feeds on caps of cultivated mushrooms (Popenoe, loc. cit.) Porcellio laewis Koch. Dooryard sowbug. Sometimes feeds on caps of ln mushrooms. (Popenoe, loc. cit.) 5 ORTHDPTERA. Ceuthophilus pacificus Thom. Reported as eating into caps of cultivated mush- rooms on Pacific Coast. (Popenoe, loc. cit.) *Proc. Ag ee Wash., vol. 33, pp. 1-20; vol. 34, pp. 59-62; viol. 34, pp. 85-88; vol. 34a 4 pp. 167-72. a THE CANADIAN ENTOMOLOGIST 199 DIPTERA Family Phoridae Aphiochaeta albidihalteris Felt. Injurious to cultivated mushrooms. (Popenoe) Sciara multiseta Felt. Injurious to cultivated mushrooms. (Popenoe) Sciara agraria Felt. Injurious to cultivated mushrooms. (Popenoe) COLEOPTERA Family Staphylinidae Philonthus cyanipennis Fab. Feeding on Russula sp. Lakehurst, N. J., June 30. Tachinus fimbriatus Grav. Feeding on Russula sp. Lakehurst, N. J., June 30. Boletobius cinctus Grav. Feeding on Russula and Collybia sp. Lakewood, N. J., June 30. Family Scaphidtidae Scaphisoma suturalis Lec. On Clavaria sp. Monmouth Jc., N. J., August 6. Family Nitidulidae Psilopyga nigripennis Lec. Occurs in the stink horn fungus. (Col. Ind. p. 646) Psilopyga histrina Lec. Occurs in the stink horn fungus. (Col. Ind. p. 645) Pocadius helvolus Erichs. Occurs in Lycoperdon giganteum. (Col. Ind. p. 644) Carpophilus antiquus Mels. On the black fungus on ears of corn. Clementon, Parnes 10,. Comith; dus.,- N» J., p: 271) Family Erotylidae Tritoa biguttata Say. Feeding on Russula and Collybia sp. Pabeiuieen Nisk; June 30. Family Tenebrionidae Platydema ruficorne Sturm. Feeding on Russula and Collybia sp. Lakehurst, Ne ., June 30. Family Anobiidae Dorcatoma setulosum Lec. Breeding in old Polyporus cuticularis. East Mill- stone, N. J., April 7. Eutylistus tristriatus Lec. Breeding in old Polyporus fuer East Millstone, ay april 7. Family Cisidae Plesiocis cribrum Csy. Breeding in Polyporus volvatus on pine stump. Lake- hurst, N. J., June 30. AN UNDESCRIBED PLANIDIUM OF PERILAMPUS FROM CONOCEPHALUS (HYM.) BY NORMA FORD, University of Toronto. An interesting phase in the life history of parasitic Hymenoptera, of comparatively recent discovery, is the occurrence of the “planidium” stage of certain Chalcidoid genera, notably Perilampus, Psilogaster and Orasema. 'The life histories in which this stage appears are suggestive of the oil beetles ( Meloid- ae) which hatch from the egg as free-living larvae, seek their host, and then become parasitic and helpless. nize AK 200 THE CANADIAN ENTOMOLOGIST The first discovery in connection with this type of life history in the Chalcidoidea was made by Prof. Wheeler (1907). While engaged in studying the life history of Orasema viridis Ashmead, a parasite of the harvesting ant (Pheidole instabilis Emery), he found proof of an early free-living stage. This stage he termed the planidium, from the Greek meaning a diminutive wan- derer. Orasema belongs to the Eucharidae, a family closely related to the Peri- lampidae. The Eucharidae are parasitic upon ants. The planidium in this case is less than 0.1 mm. in length. Prof. Wheeler found it difficult to determine the number of body segments, because of the telescoping, but he stated that there are probably thirteen. The head segment bears short mandibles and the termin- al segment has a pair of caudal setae. In 1912 H. S. Smith (712) found the planidium of Perilampus hyalinus Say as a secondary parasite of the tachinid and ichneumonid parasites of the fall webworm. The planidium was less than 0.3 mm. in length, oblong in shape, and dark brown in color. It was highly organized with a distinct head, 12 body segments, well-defined mouth parts, strong curved mandibles. The head was armed with curved hooks; the most of the plates bore pairs of bristles and vent- rally there were projecting spines, the latter evidently functioning in Iocomo- tion. There were no legs. In tracing out the life history, Smith found the planidia in the earliest stages on the exterior of the fall webworm, later within their bodies whether they were infested by primary parasites or not. Still later the planidia were en- doparasitic within the larvae of the parasites, and finally ectoparasitic after the larvae had left the fall webworms and pupated. How the planidia came to be located upon the skin of the caterpillars, and where the eggs are laid, have not been ascertained. It is thought that the eggs are laid on the leaves of plants in the vicinity of a caterpillar colony. In the course of his investigations, Smith found a second species of plani- dium which he was unable to rear, and which he terms Perilampus “species A.” In 1915 Thompson described a planidium which was attached to the in- tegument of a Noctuid, feeding on witch-hazel. This species of planidium is slightly larger, being 0.35 mm. by 0.13 mm. A most important difference is that this form has fourteen segments. ‘The details of structure are also quite different, and as follows: ‘The dorso-lateral plates which do not extend over the ventral surface, terminate abruptly. ‘The setae arise dorsally from the inter- segmental membrane, not from the plate, although there are unchitinized spots on the plates, which, however, do not give rise to setae. The ventral setae and spines show an arrangement quite different from Perilampus. In the head seg- ment ‘Thompson was able to follow in some detail the mouth parts, figuring and describing the epipharynx, superior and inferior lips, mandibles, maxillae and palpi. Dorsally on the head he identified a pair of antennae. In 1919 Prof. Brues briefly described from a cast skin the planidium of Psilogaster fasciiventris Brues, a member of the Eucharidae and a parasite of the Australian Buil-dog Ant, Myrmecia forficata Fabr. Prof. Brues does not figure the planidium, but he states that it is similar to that of Perilampus. In fact he says that this stage of Psilogaster is almost as close to that of Perilamp- ee as. ee a oe THE CANADIAN ENTOMOLOGIST 201 us hyalinus as the latter is to Perilampus “species A,” figured by Smith. Prof. Brues suggests that it may be possible that “species A” is not a true Perilampus, as Smith did not succeed in rearing an adult. While investigating a problem on the musculature of the Orthoptera, as post-graduate work with Prof. E. M. Walker, specimens were found parasit-- ized by planidia. In this case the planidia were within the bodies of one of the small green grasshoppers, Conocephalus fasciatus (De Geer) (Xiphidium fas- ciatum). The Conocephali had been collected on September 14, 1921, in the Muskoka district at Port Sydney, Ontario. Out of nine specimens, six were parasitized. The planidia from Conocephalus are very similar to those of Peri- lampus hyalinus, resembling this species more closely than the planidia of the unknown “‘species A,” or of the Noctuid or of Orasema. A careful comparison with the figures of Perilampus hyalinus, however, reveals distinct difference from that species. Fig. 1—Planidium of Perilampus from Conocephalus. From left to right, dorsal, lateral and ventral views. The planidia from Conocephalus average 0.21 mm. in length, and 0.07 in diameter. Measurements of eight specimens were as follows: 0.23 x 0.07, 0.21 X 0.06, 0.19 x 0.08, 0.20 x 0.07, 0.20 x 0.06, 0.22 X 0.07, 0.21 x 0.07, 0.16 x 0.04mm. ‘The body is composed of thirteen segments, dark brown in color. ‘The head segment is emarginate posteriorly and bears two pairs of recurved hooks. - The posterior pair correspond to the structures which Thompson identified as an- 202 THE CANADIAN ENTOMOLOGIST tennae, but in this species they are merely pointed hooks. Behind each hook of the posterior pair is a semi-transparent spot, followed by two smaller spots and then by a pair of large contiguous spots. There is also, on either side of the head, a lateral spot and a ventral-lateral hook. The mouth-parts are difficult to determine. It would seem that the large curved mandibles are supported by a cross-bar of heavy chitin and that a dis- tinct mouth-tube is present. Between the mouth-tube and the mandibles pro- ject forked structures which are probably maxillae. Each body segment consists of a heavily chitinized tergite with a toothed ven- tral border and of an unchitinized sternal region provided with strong re-curved hooks. On the tergites are semitransparent spots each bearing a seta. These spots have a definite arangement in two rows—a dorsal and a ventral. The spots of the dorsal row are dorso-lateral in position and situated on the odd segments, I, 3, 5, 7, and 9 and also on segment 2. The pair of spots on seg- ment 2 are again exceptional because of their more dorsal position. The ventral row consists of spots ventro-lateral in position and situated on consecutive seg- ments, I, 2, 3, 4, 5,6, 7, 8 and g. An exception is found in segment 3 where the spots lie in a more ventral position and there is a third pair of spots srruated on the extreme ventral portions of the tergite. The two spiracles open dorso-laterally in the membrane connecting seg- ments I and 2. In the sternal region are groups of hooks segmentally arranged. The hooks of segment I are the largest and are arranged in two rows. Three hooks in the posterior row are much larger than the others, are attached by broad bases and taper into sharp re-curved points. Lateral and anterior to these are smaller hooks, varying in number in the anterior row from 3 to 5. In segment 2 the number varies from 8 to 9 in the anterior row and from II to 12 in the posterior row. In the remaining segments the number of hooks gradually decreases. The caudal setae are about six times the length of the last segment. Comparing the planidium from Conocephalus with the planidtum of P. hyalinus, the noteworthy points of difference are as follows: The planidium of hyalinus is larger and more slender, averaging 0.3 mm. in length and 0.06 mm. in diameter at the widest place, (as compared with 0.21 mm. in length and 0.07 mm. in diameter). The head segment lacks the lateral pair of semitransparent spots and ventro-lateral hooks. The dorsal row of spots on the tergites is similar in the two forms, but the spots of the ventral row on P. hyalinus extend only to segment 8, and in addition segment 8 bears a third pair of ventral spots, while on segment 3 the third pair is lacking. The spiracles are ventral in hyalinus instead of dorso-lateral, and the caudal setae are only twice the length of the last segment. The planidium of “Species A” is quite different in structurural details from those just considered. The head segment is not emarginate, the ventral borders of the tergites are not toothed, the ambulatory spines are much less developed. The spots of the dorsal row on the tergites have a different arrangement being on segments I, 2, 3, 4, 5, 6, 8 and 10, while those in the ventral row have an ar- rangement similar to that of the planidium from Conocephalus, being on con- ian eS a ae "oe Te eee ee Tees ea ee ae ee ae iz a 2 fay ae) _ Syere THE CANADIAN ENTOMOLOGIST 203, secutive segments, I, 2, 3, 4, 5, 6, 7, 8, and 9, with a third pair of spots on seg- ment 3. Of the six parasitized specimens only one has been fully dissected. Seven planidia were found in the body, one lying in the connective tissue of the meso- thorax, a second embedded in the sternal muscle of seg. 4, a third lying near the nerve cord in seg. 6, a fourth in the connective tissue near the intestine in seg. 6, while the fifth, sixth and seventh were in the sternal muscles of seg. 7. Smith found the planidia in almost any position in the caterpillar’s anatomy, although they generally floated out freely in the body cavity. If the planidia also floated freely in the body of Conocephalus, many may have been lost since the speciments had been opened and pinned ready for musculature dissections and then preserved in alcohol. It is quite improbable that the true host of Perilampus is Conocephalus. It would seem rather that the planidium must require some parasite of Conocephalus in which to complete its development. This view is supported first by the fact of the life history of P. hyalinus and Orasema. The planidium of P. hyalinus lives at first within the body of the dipterous or hymenopterous host, but does not feed. When the host changes into the pupa, the planidium then emerges, lives ectoparasitically and commences to feed, protected by the puparium or the co- coon. The planidium of Orasema lives entirely ectoparasitically upon the pupae of soldiers, males or females of the harvesting ant, where the young planidium is usually found attached to the intersegmental membrane near the head. Comparing the life history of Perilampus and Orasema, it is evident (as _Thompson pointed out), that the stage spent by Perilampus in the body of the fall web-worm and the host is merely a prolongation of the migratory period in the life of the planidium, since the parasite neither grows nor feeds and can not complete its development until it becomes ectoparasitic. In view of these facts of life history it is quite improbable that Conocephalus is the true host, for a development comparable to those just described would be impossible. One would expect that the planidium is seeking in the body of ~Conocephalus the larva of some parasite of the latter. As evidence for this theory we searched for records of the parasites of Orthoptera. In 1910 Swenk (11) reared P. hyalinus from an undetermined sarcophagid which in turn was reared from Melanoplus bivittatus. In 1914 an important paper was published by Kelly (1914) based on his investigations of the sarcophagid parasites of grass- hoppers. As hosts he found Schistocerca americana, Melanoplus atlanis, M. femur-rubrum, M. bivittatus, M. differentialis and Dissosteira longipennis. As an example of his records he states that in June 1913 there was quite a serious outbreak of grasshoppers, the prevalent species being Melanoplus differentialis, M. bivittatus and M. atlanis, with a few scattering individuals of other species. “The ground was strewn with dead nymphs and adults of the three species men- tioned, which had died from parasitism of sarcophagids, their bodies being alive with maggots, while the fields were literally swarming with these flies engaged in striking adults and nymphs of each instar, except the first. Deposition of the larvae by the sarcophagid took place only while grasshoppers were flying or hopping.” This last observation is important as evidence that it is not the 204 THE CANADIAN ENTOMOLOGIST dead bodies that flies attack. Kelly demonstrated that the sarcophagid flies will strike at any moving object—at moths, butterflies, cicada or a piece of crumpled tissue paper. He threw into the wind such a paper and no less than six flies struck it. When the paper was examined, two tiny maggots were found cling- ing to it. From some 800 dead grasshoppers collected nearly 1,200 Sarcophaga of several species issued. Kelly also observed four species of Sarcophaga ovipositing on the adults and nearly grown nymphs of Chortophaga viridifasciata, during late April and early May. Adults of these species of parasites issued from the first week in June till the first week in July. It was judged that there are probably five or six generations for the season. Kelly reared Perilampus hyalinus as a secondary parasite from the Sar- cophagids. Many records from numerous observers are brought together in Kelly’s paper, and although there are no records of the Sarcophagids being reared from the long-horned grasshoppers, yet is is probable that they too are parasitized. Regarding the planidium from Conocephalus, we shall attempt this summer to investigate its life history further and hope to rear the adults. In following out this work I am much indebted to Prof. E. M. Walker for his advice and help. I wish also to thank Dr. L. O. Howard and Mr. S. A. Rohwer for refer- ences in the bibliography. BIBLIOGRAPHY. 1907. W. M. Wheeler, “The Polymorphism of Ants.’’ Bull. of the Amer. Mus. =~ -OL Nat. Histi, vol: 235 Ate «11007. tgit. M. H. Swenk, “Notes on Some Insects Injurious in Nebraska in 1910.” Journal of Economic Entomology, vol. 4, p. 2860. : 1912. H.S. Smith, “Technical Results from the Gipsy Moth Laboratory. 1V. The Chalcidoid Genus Perilampus and Its Relations to the Problem of Para- site Introduction.” U.S. Dept. Agr., Bur. Ent. Tech. Ser. No. 19. 1914. E. O: G. Kelly, “A New Sarcophagid Parasite of Grasshoppers.” Jour. Agric. Research, U. S. Dept. Agric., Vol. IT. : 1915. W. R. Thompson, “Contribution a la Connaissance de la Larve Plani- dium.” Bull. Sci. de la France et de la Belgique, tome 48. 1919. C. T. Brues, “A New Chalcid-fly Parasitic on the Australian Bull-dog Ant.” Ann. Entom. Soc. America, Vol. 12, pp. 13-21, Pls. 2. APPOINTMENT TO ENTOMOLOGICAL BRANCH, OTTAWA, Canadian Entomologists will be pleased to learn of the appointment of. Mr. C. H. Curran of Orillia, Ontario, to the position of Assistant Entomologist in the Division of Systematic Entomology, Entomological Branch, Ottawa. Mr. Curran, who has a well-earned reputation as a specialist in the Syrphidae, will have immediate charge under Dr. McDunnough, of the Diptera in the Canadian National Collection. 1 AG 206 THE CANADIAN ENTOMOLOGIST NOTES ON THE RELATIONSHIPS INDICATED BY THE VENATION OF THE WINGS OF INSECTS BY G. C. CRAMPTON, Massachusetts Agricultural College, Amherst, Mass. Comstock and his students, and such investigators as Handlirsch, Tillyard, and others, have made available for comparison practically all of the more im- portant types of wing-venation occurring in the different orders of insects; and | in the following discussion, I would make use of the interpretations of the veins -by these investigators, to point out wherein the evidence of the wings figured by them would support certain conclusions concerning the origin and interre- — lationships of the insectan orders, which I have reached from study of the parts of the body in general. While I feel that the interpretations of the veins, par- ticularly the cubital and anal ones, (and more rarely the median veins also) are not correct in some cases, I have, nevertheless, followed the interpretations giv- en by these investigators in each case, since my sole purpose at this time is to point out the similarity between the wings of certain insects, in support-of my contentions as to the interrelationships of these forms, based upon the structures of other parts of the body; and the interpretations here given will in most cases serve the purpose sufficiently well. The Palaeodictyoptera are considered by most of the recent students ofa venation as the direct ancestors of all other Pterygotan insects, and Handlirsch even considers them as ancestors of the Apterygota also. While the Palaeo- dictyoptera have departed but little from the types ancestral to the rest of the Pterygota, I do not think that they represent the actual ancestors of all other winged insects, and I am more inclined to regard them as a primitive group which branched off at or near the base of the common Pterygotan stem. The Protodonata, (fig. 62) which are a primitive Odonatan type leading to the modern Odonata, are regarded as a distinct order by recent investigators, but I do not think that the character of the body in general of the Protodonata is _ sufficiently different from recent Odonata to justify placing them in a distinct order. The Protephemerida (fig. 63) on the other hand, seem to be different enough from their descendants, the Ephemerida, to be grouped in a distinct ord- er. The Protephemerids and Protodonata are thought to be the descendants of the Palaeodictyoptera, but many of them have retained characters as primi- tive in some respects as the Palaeodictyoptera, and it is much more probable that the Protephemerida, etc., are descended from ancestors like those of the Palaeo-_ dictyoptera, rather than that the Protephemerida etc., are the direct descendants of — the Palaeodictyoptera themselves. Certain immature Ephemerids exhibit char- acters extremely like those of Lepisma, Machilis, and other Apterygota which have departed but little from the condition typical of the ancestors of the first Pterygotan insects, and in many respects these immature Ephemerids are among the most primitive known Pterygotan forms. The wings of both Protodonata and Protephemerida are usually polyneurous, and the venation in the Protodon-— ata in particular tends toward the unilateral type of branching. The venation of the Protephemerida, however, is not as similar as one might expect, and the ‘ - 33 a ~~ oe ~ » eng iat. 5 —" i, oS — Fig .% a werk ie ‘* Be ¥ 207 PLATE 6 — > LAOS & a = VENATION OF INSECT WINGS. 5 208 THE CANADIAN ENTOMOLOGIST relationship between the two groups is not as close as is maintained by some in- vestigators, nor does either type of venation approach that of the Plecoptera to any marked degree, so that the grouping of the Plecoptera with the Odonata and Ephemerida on the basis of their immature stages being aquatic, is a very artificial one, and apparently has no real phylogenetic significance. The vena- tion of the Protodonata (and to some extent that of the Protephemerida) is rather suggestive of that of the Neuroptera in some respects, but the resernblance in this case is probably due to their mutual relationship to the Palaeodictyoptera. The lines of development of the Protodonata and Protephemerida apparently branched off at a very early period in the evolution of the Pterygotan types, and neither seems to be of any great value in the study of the evolution of the other Pterygotan types. The Protodonatan-Odonatan line of descent in partic- ular is a very isolated one, leading along a path of specialization which does not approach very closely to that of any other group of insects, although the Prot- ephemerid-Ephemerid line of development probably represents their nearest of kin (other than the Palaeodictyoptera), and the slight resemblance of the vena- tion of both groups to that of certain Neuroptera is doubtless the result of con- vergent development. The common ancestors of the Protoblattids and Protorthoptera are per- haps the most important of all insects for a study of the evolution of winged insects in general, since these two types exhibit many tendencies which were ap- parently carried over in the lines of development of the higher forms (so far as the wing venation is concerned) and a surprisingly large number of lower types apparently parallel their lines of development. If the hypothetical common an- cestral stock from which the slightly diverging lines of the Protoblattida and Protorthoptera were descended be designated for convenience as the “Prodicty- optera,”’ it would appear that the ancestors of these “Prodictyoptera” were re- lated to the Protodonata and Protephemerida as well as to the Palaeodictyoptera, but their closest affinities were apparently with the Palaeodictyoptera. The Pro- toblattida are apparently somewhat nearer to the common ancestral stock than the Protorthoptera are, and the polyneurous tendency is the strongest in the Pro- toblattida, while many of the so-called Protorthoptera are markedly oligoneurous (if all of the forms called “Protorthoptera” by Handlirsch are really Protorthop- tera—which seems very doubtful), and are quite highly specialized in their vena- tion for such ancient insects. The wings of both Protoblattida and Protorthop- tera are usually markedly “heteronomous,” and in the hind wings of these forms (figs. 23, 29, 24, etc.) the precursor of the huge anal fan of the Orthopteroid insects makes its appearance. Not only does the common ancestral stem of the Protorthoptera and Pro- toblattida form the central point about which the ancestors of recent insects are gathered, but many of the lines of descent of the earlier fossil orders are clust- ered about these forms, and their lines of descent in many instances parallel that of the Protorthoptera (and to a less degree that of the Protoblattida also) rath- er closely. Thus, the Synarmogoida (fig. 3) approach the ancestors of the Prot- orthoptera in many features, while they are clearly like the Palaeodictyoptera in other features. ‘The character of the subcosta (Sc), radius one (R,), and the 210 THE CANADIAN ENTOMOLOGIST radial sector (Rs) of Fig. 3 clearly suggests affinities with the Orthopteron shown in Fig. 2, while media and cubitus of Fig. 3 are like these veins in cer- tain Protorthoptera—although the latter veins are more like those of the Palaeo- dictyoptera than those of the Protorthoptera. The character of the anai veins in Fig. 3 are as much like those of the Protorthoptera (and Protoblattids) as any insects, and taking their venation as a whole, the wings of the Synarmogoi- — da would indicate that their line of descent arose near the base of the common stem of the Protorthoptera and Protoblattida at the point where these forms. diverged from the Palaeodictyoptera, in emerging from their common ancestry. While the line of descent of the Synarmogoida parallels that of the Protor- thoptera in certain respects, the Synarmogoida are a more or less isolated group. of no great value for the study of the evolution of recent insects. The venation of the Hapalopteroida as shown in Fig. g resembles that - of the Protorthoptera and Orthoptera shown in Figs. 6 and 2 quite closely. It likewise exhibits certain points of similarity to the Mixotermitoid shown in Fig. 13, and there is also a slight resemblance to the Plecopterous wing shown in Fig. 8, but the Hapalopteroid line of descent is apparently a rather isolated one hay- ing no great value in tracing the lines of descent of recent insects. The Hapal- opteroida possibly branched off from the base of the common Protorthopteron- Protoblattid stem near the point where the latter began to diverge from the Palaeodictyoptera, and the Hapalopteroid line of development parallels that of the Protorthoptera rather closely, and also approaches that of the Mixotermi- toida in some respects. The Mixotermitoida (figs. 13 and 17) resemble the Protorthoptera (figs. 6, 19, and 2) quite closely, and they also exhibit certain features of resemblance to the Hapalopteroida (fig. 9) and to the Reculoida (fig. 7) as well. There is a slight resemblance to the MHadentomoida (fig. 21) also, but the re- semblance is not marked. The closest resemblance is to the Protorthoptera, and the line of descent of the Mixotermitoida probably sprang from a point near the base of the common Protorthopteron-Protoblattid stem, where the lat- ter began to diverge from the Palaeodictyoptera, and the Mixotermitoid line of development parallels that of the Protorthoptera and Hapalopteroida as close- ly as any. The-group is of no particular interest for the study of the evolution of recent insects. Practically all of the features exhibited by the Sypharopteroida (fig. 4) occur in the wings of some Protorthoptera (such, for example, as the short subcosta, long radius, one unilaterally branching radial sector, single-““branched” media, etc.) They also resemble the Mixotermitoida (fig. 13) and Megasecop- tera (fig. 1) in some respects. The line of descent of the Sypharopteroida ap- parently arose at the point of divergence of the common Protorthopteran-Pro- toblattid group from the Palaeodictyoptera, and paralleled the line of develop- ment of the Protorthoptera very closely. The fossil shown in Fig. 5, which Tillyard regards as a Protorthopteron, exhibits points of resemblance to both Protorthoptera and Sypharopteroida. The wing of the Hadentomoid shown in Fig. 21 is somewhat like that of the modified descendant of the common Protorthopteron-Protoblattid stem, ete net Se , a in eee poe ere ee a ee ey ee eee ey ee ee WN) iy NN \ sy ui s . = Se, =e; § _ wy __ 66 “B1y ’ SN 2 —————S = 5 N —— = ¥ = aS va ZF Z u G - L.-9 Zz < w_%) nDsy “Bly = 5, 212 THE CANADIAN ENTOMOLOGIST shown in Fig. 14, and it is also faintly suggestive of the Mixotermitoida (figs. 13 and 17) and Hapalopteroida (fig. 9) in some respects. It is somewhat more like the Protorthopteron Lepium (not figured here) however, and the Hadento- moida probably arose near the base of the common Protorthopteron-Protoblattid stem at the point where the latter diverged from the Palaeodictyoptera. The Hadentomoida exhibit certain features suggestive of a relationship to the Plecop- tera (figs. 22 and 8), and also to the Embidiina (fig. 18), so that their line of development is of some interest for the study of the evolution of certain recent forms. The Reculoida (fig. 7) resemble the modified descendant of the common Protorthopteron-Protoblattid stem shown in Fig. to, and they also resemble the Protorthoptera (fig. 6) quite closely. Their line of descent probably branched off near the point of divergence of the common Protoblattid-Protorthopteran stem from the Palaeodictyoptera, and their line of development parallels that of the Protorthoptera fairly closely. The wing of the Megasecopteron shown in Fig. 1 is perhaps as much like that of a Palaeodictyopteron (fig. 30) as any other, but it clearly approaches the Protorthopteran and Orthopteran types (fig. 2) in the tenden- cy for media to unite with the radial sector, arid for cubitus to unite with media. The Megasecoptera resembles the Sypharopteroida (fig. 4) in certain respects, and they also bear a rather faint resemblance to the Protephemerids and Synarmogoida (fig. 3) in certain features, but their closest affinities are with the Palaeodictyoptera and Protorthoptera, and their line of develop- ment apparently arose near the point where the Palaeodictyoptera began to diverge from the common ancestors of the Protorthoptera and Protoblat- tida, and paralleled the line of development of the Protorthoptera. rather close- ly, while it approached the lines of development of the Sypharopteroida and Synarmogoida only slightly. Since certain tendencies observable in the Me- gasecoptera find opportunity for fuller expression in the Neuropteroid insects, the study of the Megasecoptera is of considerable value in tracing the origin of the higher insects. ; In taking up the consideration of the evolution of recent insects, we find that here also; the study of the venation of the Protoblattida and Protorthoptera is of prime importance, as was likewise the case in studying the evolution of the earlier fossil forms, since the lines of development of recent forms as well as the earlier fossil types, tend to group themselves about the Protoblattida and Protorthoptera, which, judging from their wings, were a variable group in an active state of evolution. I have grouped the recent orders Blattida, Man- tida and Isoptera into a single superorder (the “Panisoptera’’), and 1 would point out the fact that the evidence of the venation of the wings is in full ac- cord with that drawn from a study of other features of the body, which indi- cate that the group mentioned above is a natural one. The wings of the Pro- toblattida clearly indicate that the Protoblattids are the nearest representatives of the precursors of the Blattida, and if one compares the hind wing of the Mantid shown in Fig. 27, with that of the Protoblattid shown in Fig. 24, it is quite evident that the Protoblattids are the nearest representatives of the pre- cursors of the Mantids also; and both Blattids and Mantids apparently arose 213 THE CANADIAN ENTOMOLOGIST PLATE 9. NT. VoL. LIv. Can. E VENATION OF INSECT WINGS. 214 THE CANADIAN ENTOMOMOGIST from the same source in the common Protoblattid-Protorthopteron stock. Simi- larly, the hind wing of the Isopteron shown in Fig. 26 is very similar to that of the Protorthopteron shown in Fig. 29, and also resembles extremely closely the hind wings of the Protoblattid shown in Fig. 23. The Isoptera, therefore, in all probability arose from the same source in the common Protoblattid-Protor- thopteron stock which gave rise to the Blattids and the Mantids. Although the alaflabellum, or anal fan, of the Isopteron shown in Fig. 26 is not typical of all Isoptera, the termite there figured is a very primitive one, and its condition clearly indicates that certain of the ancestral Isoptera had well developed alafla- bellum, which they evidently inherited from ancestors of the common Protor- thopteron-Protoblattid stock. The precursor of the anal fan of the Protoblattids and Protorthoptera is suggested by the broadening of the basal portion of the hind wings of such Palaeodictyoptera as the one shown in Fig. 50, but it is not very probable that this Palaeodictyopteron represents very closely the type which gave rise to the common Protorthopteron-Protoblattid stock. ‘The alflabellum is enormously deve- loped in the Orthopteroid descendants of the Protorthopteron-Protoblattid stock (figs. 48, 49 and 45) and it is also large in the Plecopteron shown in Fig. 46 (which was also derived from ancestors resembling the Protoblattids and Pro- torthoptera in many respects. ) I have grouped the Plecoptera and Embiidina in a common superorder (the ““Panplecoptera”), and the venation of the wings would clearly support such a grouping, as may be seen by comparing the wing of the Plecopteron shown in Fig. 22 with that of the Embiid shown in Fig. 18. Both of these wings resemble that of the Hadentomoid shown in Fig. 21, rather closely, and the wings of the Plecoptera (figs. 22 and 8) are rather suggestive of the Hap- alopteroida (fig. 9) in some respects. The Plecoptera, however, in all probabil- ity were derived from ancestors closely resembling the common Protorthopter- on-Protoblattid stock (and also related to the Palaeodictyoptera) from which the Isoptera were descended, since the wing of the Plecopteron shown in Fig. 8 is extremely similar to that of the Isopteron shown in Fig. 12, and both lead back to the Protorthopteron-Protoblattid types shown in Figs. 19, II, 15, ete. If the termite-like insect shown in Fig. 16 is really a Neuropteron, the venation of some Neuroptera evidently approach the type of Isopteran and Plecopteran venation shown in Figs. t2 and &, thus suggesting that the origin of the Plec- optera was not far from the point of origin of the Neuroptera also. The huge anal development in the hind wing of the Plecopteron shown in Fig. 46 would indicate that the primitive Plecoptera sprang from the same stock which gave rise to such Blattids as the one shown in Fig. 42 (and 43), thus lending further weight to the view that the common Protorthopteron-Protoblattid stock repre- sents quite closely the ancestors of the Plecoptera (and their allies the Embiidina), and the lines of development of the Plecoptera and Embidiina parallel those of the Protorthoptera and Protoblattida quite closely, while they approach the Had- entomoida and Hapalopteroida only slightly. It should be borne in mind that the Kmbiid type of wing approaches the Isopteron type almost as closely as the Plecoptera mentioned above do, but it has not seemed necessary to include fur- THE CANADIAN ENTOMOLOGIST 215 ther figures to demonstrate this fact, since it is quite patent that the Embiidina and Plecoptera are so closely related that what applied to one applies to the other, as well. The Dermaptera, Phasmids, Grylloblattids, and saltatorial Orthoptera are here grouped in the superorder ‘“‘Panorthoptera.”” The Dermaptera were form- erly grouped with the Embiidina and Plecoptera, but it is preferable to place them nearer the Phasmids, saltatorial Orthoptera, etc., than was done in the former grouping. In the enormous development of the anal area, and the ac- companying reduction of the preanal region (i. e. the region in front of the anal area) the Dermapteron wing shown in Fig. 48 approaches the Orthopteron and Phasmid shown in Figs. 45 and 49, and the “floating” or intercalary veins, which are not attached basally, and occur between the anal veins (of which they are probably detached branches), are rather similar in the insects in ques- tion. ‘The paramarginal line extending almost parallel to the margin of the wing in the insect shown in Fig. 48, was possibly formed by the joining, end-to- end, of certain of the cross veins, some of which are shown in Fig. 45. The wings of the Dermaptera (Fig. 48) likewise approach the Blattid wings shown in Figs. 43 and 44, and they are also suggestive of the wing of the Plecopteron shown in Fig. 46. From these resemblances, we may conclude that the Dermap- tera arose from the common Protorthopteron-Protoblattid stem very near the point at, whick the lines of development of the Phasmids and saltatorial Orthop- tera branched off, but the general character of the body in general would pre- clude the possibility of deriving the Dermaptera from saltatorial Orthoptera. It is likewise very probable that the line of development of the Dermaptera arose near the point of origin of that of the Blattids and of the Plecoptera (with the Embtidina) as well, and this would account for the general resemblance cf the Dermaptera to the Plecoptera and Embiida, as well as to the Blattids, Mantids and Isoptera, since they all arose near the same point, though the line of develop- ment of the Dermaptera follows that of the Phasmids and saltatorial Orthoptera (with the Grylloblattids) more closely than any other forms. In this connection, it may be mentioned that the Hemimeridae are merely modified Dermaptera, and the Grylloblattids are probably very primitive Orthoptera closely related to the Protor- thoptera and Protoblattids. The wings of the Phasmids (Fig. 49) would in- dicate that their closest affinities are with the saltatorial Orthoptera (Fig. 45), although in the general character of their external anatomy, they are extremely closely related to the Grylloblattids and Dermaptera, and likewise exhibit cer- tain points of resemblance to the Plecoptera and Embiids, as well as to the Man- tids, Isoptera, and Blattids (compare also the wings shown in Figs. 43, 42, and 46 with Fig. 49.) The Phasmids apparently sprang from the common Protor- thopteron-Protoblattid stock very close to the point where the true Orthoptera (with the Grylloblattids) and Dermaptera arose, and also not far from the point of origin of the Blattids (with the Mantids and Isoptera) and the Plecoptera (with the Embiidina) also. The line of development of the Phasmids, however, parallels that of the saltatorial Orthoptera (with the Grylloblattids) extremely closely; and the wings would indicate that their closest allies are among the saltatorial Orthoptera and Dermaptera, and also that the Blattids are their next closest allies. ‘The body in general of the Phasmids is much more primitive 216 : THE CANADIAN ENTOMOLOGIST than that of the saltatorial Orthoptera, and it is infinitely more probable that the Phasmids branched off near the base of the Orthopteran stem, than that the Phasmids were derived from the saltatorial Orthoptera. (To be continued.) THE PERMANENT BUREAU OF ALL-RUSSIAN ENTOMO-PHYTO- PATHOLOGICAL CONGRESSES IN PETROGRAD, RUSSIA. es The Permanent Bureau of All-Russian Entomo-Phytopathological Con- as gresses, Liteyny, 37-39, Room 59, Petrograd, Russia, desires: 1. To exchange printed matter (published since 1914) on entomology, phytopathology, mycology and zoology, with American colleagues, Scientific So- cieties, Agricultural ig SES Stations, Museums of Natural History, periodi- cals, etc. 2. To receive from American publishers catalogues and specimen num- bers of various publications on the above mentioned subjects. 3. To receive catalogues and price-lists from American firms dealing in various apparatus and chemicals used in combating the plant injurers. The above mentioned Permanent Bureau has supplied credentials to Mr. +. D. N. Borodin (who also represents the Bureau of Applied Botany of the Rus- | sian Agriculatural Scientific Committee, Petrograd) to collect literature in this country and give all the necessary information to the American colleagues, con- cerning entomological work conducted in Russia, and to organize an exchange of literature. ; Mr. Borodin will accept all packages with books, bulletins, etc. for Russia, if they. will be addressed to him at No. 110 West 4oth Street, Room 1603, New York City. BOOK NOTICE Volume X, No. 1 of the University of Iowa Studies contains three ento- mological articles. ie Report on the Scutelleroidea collected by the eae -Antigua Expe- dition in 1918 by Dayton Stoner. Seventeen species are recorded. The report is well illustrated and many interesting observations on the habits, food plants and distribution of the various species are given. EL: ae on the Orthoptera and Dermaptera of the same Expedition by A. . Caudell. , di Se species are treated of, distributed as follows :—Forficulidae, 2 Blattidae, 8; Mantidae, 2; Phasmidae, 2; Acrididae, 7; Tettigonidae, 3; Gryllidae, 7. One new species of Blattidae, Eurycotis similis, one new Acridian, Ambly- tropidia stoneri, and two new Gryllids, Cycloptilum minimum and Het- erecous? dubius are described. Ill. ‘The Scutelleroidea of the Douglas Lake Region by Dayton Stoner. " Twenty-seven species are listed as occurring in the vicinity of this north- ern Michigan Lake and numerous valuable ecological notes are given — under the various specific headings. ; J. McBS Nailed Thursday, November 23rd 1922, ‘ a i VOL. LIV. ORILLIA, OCTOBER, 1922. No. Io. POPULAR AND PRACTICAL ENTOMOLOGY Tur CocKLEBUR BILLBuc* BY F, H. CHITTENDEN, U. S. Department of Agriculture. The excessive price of commercial oils during war times led to more ex- tensive cultivation of oil-producing plants, such as the castor bean and sunflower. The seeds of the latter are cultivated in Kansas and neighboring States in the Middle West and the oil therefrom utilized for the manufacture of oil-cake for lighting purposes, for woollen dressing, candle and soap-making. The oil-cake and seeds are useful foods for stock and poultry, and the seeds also for cer- Fig. 1—Rhodobaenus 13- punctatus: a, common form of beetle; b, head and beak of female; c, same of male—all enlarged. tain cage birds. Complaints have been made during recent years in regard to weevils which affect cultivated sunflower. For several years past the writer has had under observation a rhynchophorous larva which inhabits the stems, known as the cocklebur billbug (Rhodobaenus 13-punctatus Ill.). The following notes: are submitted as of interest in connection with the growing of sunflower for commercial use. *Rhodobaenus tredecimpunctatus [l\l.; family Calandridae; order Coleoptera. - » os se eee - esene” 2 = yy ‘ > -_ ae 2 SO ee re ae : * ee = ara pS f aK ons cy ra 2 OG —s if 218 "DHE CANADIAN ENTOMOLOGIST See OSE : ies was injurious to dahlia. All of his plants had Sey eter by the laid described as boring upwards through the pith of the stem and then through 1 branches. This greatly injured the vitality of the plants, the stalks being wez ened, and caused the plants to break down by their own weight. What few blooms were borne were smail and inferior, and the plants were so badly infest- ed as to be of no value that year. Pupae were seen as late as August 31. Soo [ thereafter, this species came to the attention of Dr. E. G. Titus in its occurrenee on sugar beet, there being evidence that the larvae could breed in seed-s al I August-6, 1921, Mr. W. V. Reed, Assistant Entomologist, State of Georgia, this beetle from Atlanta, Ga., with statement that it was quite a pest on dah in that State. A few plants were injured by this insect in previous years, that year it had done pies considerable damage to dahlias. The weevil seemed gc dahlia stocks were more or ins young and tender. In the older stalks it beste them and lessens their vitality considerably. Larvae were about full grown at_ this time. %. THE BEETLE from the South chermnaaly occur in which these spots become tere into fiasidel From our native corn billbugs (Sphenophorus) and their allies, to which this — species is related, it may be distinguished at once by its color, its much mo: Ten strongly curved beak, and differently shaped antennae. The beetle measures usually less than half an inch in length, but specimens vary fron1 one-fourth : ~ fully one-half of an inch. : DISTRIBUTION regions, and is about equaliy common on the Pacific Coast. It does not appe to inhabit territory north of the Transition life zone, and is common in Mexi and Central America, as also in Columbia, S. A. “e The beetles are somewhat free fliers, in which respect they differ tc m1 most known species of Sphenophorus. - The first account of this species was by Riley in 1871.2 A short accow t was given by the same writer ten years later. In the latter the larval characte: are briefly indicated. : ieee Pos, ‘These on the thorax, and in pote the ‘ete are whelis black | 2 the disk. It is an exceedingly variable species, no hess that 22 synonyms and 16 forms having been recognized (Champion, Biol. Centr. Amer., Colleop., Vol. IV. pt. 7, pp. 149-150, 1910). “g 2—Riley, C. V. Third Missouri Report, p p. 60, 1871. . 3—Report Comm. Agr. for 1881-82, p. 142. 219 the ‘anal seebeat!. is protuberant, armed with two blunt terminal spines ; di is broadly rounded, not vittate, mandibles bidentate, ligula emarginate, iate ; the ocelli occupy the same relative positions upon the front margin phenophorus, but are larger, convex, lenticular, with pigment spots plainly - beneath.” In other respects the larvae of these two genera agree very ‘A even to the folds of the body-joints and the position of the occipital de- ‘hodobaenus 13-punctatus larva; a, lateral view; b, head and first thoracic segment ; c, dorsal view of anal. segment, enlarged. Foop AND OTHER Hapsrts 1880, F, M. Webster* noted the occurrence of the larva in the pith of ae the writer published a ‘fate on this insect and its occurrence in in ty of Washington, D. C.> | This species breeds in the stems of various wild plants, chiefly Compositae, i Life, Vol. 1, p. 382, 1889. 220 THE CANADIAN ENTOMOLOGIST ie £ gs ornamental dahlia. Its occurrence on sugar beet is exceptional. It is frequent- ly associated with other insects, notably with the clover stem-borer Languria mozardi Latr.). The hibernated imagos appear in the District of Columbia in early May, : and although oviposition has not been observed, judging from analogy, the eggs are deposited in holes which the female cuts in the stems while they are still young and tender. he larvae bore through the pith, and when mature forma _ cell in which they transform to pupae and afterward to adults. Newly-bred — imagos occur from the middle of August until the first week of September. NATURAL ENEMIES. ie. ‘ Two parasites of this species have been observed, the chalcidid Habrocytus 7 rhodobaeni Ashm., reared by the writer from larvae from Rosslyn, Va., and des- se cribed in 1896°, and an undescribed chalcidid. aoe NOTES ON EXYRA SEMICROCEA GUEN. AND FORM - HUBBARDIANA DYAR. (LEPIDOPTERA) : | BY F. H. BENJAMIN, Agricultural College, Mississippi. While on an inspecting trip to southern Mississippi the author had the opportunity to view these interesting little Noctuid moths in their natural habitat. be Twenty miles north of Gulfport, on the Dixie Highway, Professor Lob- SA dell, Mr. Langston and the author were examining low lands with the idea of = attempting to ascertain the extent of damage to be anticipated to crops by pe | fish. ee Here, Sarracenia flava was present in vast numbers. This is the wel = known Pitcher Plant of our southern wet lands, which annually destroys vast numbers of insects. The normal insect, entering the funnel shaped leaf, is unable — to find its way out, and is actually digested by the fluids in the bottoms of the leaves. ‘This is a most remarkable instance of plant specialization, but still more remarkable is the fact that this plant has a set of enemies belonging to the genus of moths known as Exyra who are especially adapted throughout their entire life. cycle to live within the “pitchers” of these plants. 3 Unfortunately the author was unable to view the egg laying of these pupae to adults. Heretofore, these moths were not common in collections, a they apparently are not very much attracted to light. A light burned in a localit at infested with the insects failed to attract any specimens. Most of the specimens — in collections have either been found accidentally, or carefully reared fromtary ae, outside of the native wet acid soils in which it grows. © All stages of the larvae were found within the “pitchers,” eating as ee usual thing only the protected inside tissue, and thus undoubtedly gaining a _ high degree of protection against natural enemies. Occasionally the leaf tissue i — ee 4 6—Trans. Amer. Entom. Soc., Vol. XXIII, ip. 220, 1896. THE CANADIAN ENTOMOLOGIST 221 “was eaten through, but this appeared to be an accident, rather than the normal ‘mouth of the leaf in which it lives. There is only a single individual to a leaf, although they do not appear to be carnivorous, and a number were success- A; lly carried in a tin box for several days. : When ready to pupate, the larva forms a cocoon of frass and silk, in the "slender part of the “pitcher”; having spun, just above this cocoon, a stiff web of sill which seems to be a very effective protection against disturbance from above. These stiff webs appear to be a sure indication of a pupating larva or pupa < _ below. Before pupating the larva eats the leaf so that merely a shell of very Pihin tissue, in the form of a round spot, remains between it and the outside world. vs it to be concluded that the adult pushes its way through this thin shell? Cer- “tainly the pupa does not do so, for it remains snugly within its cocoon, and is _ not found half way out of the plant, as is the case with the Cossidae. However, ee ie front of the adult is in the shape of a sharp pointed cone, undoubtedly fitted ~ for pushing its way through something, and it seems almost certain that this is - the means of emergence to the outside world. ’ After the adult has emerged, and left the old “pitcher”, it seeks a new green “pitcher” for its hiding place. It never enters an old “pitcher” unless seeking an immediate hiding place from threatened danger, and then never if fresh green “pitcher” be close at hand. It is very peculiar that these moths should always select the green leaves, from one to five adults being regularly é found within each green “pitcher”. Almost every green “pitcher” had at least one moth resting within it, whereas the only “ee a taken in old “pitchers” were moths which were frightened out of the green “pitchers” and entered the others to hide. About forty specimens were caught in the green “pitchers” in less than half an hour, surely an easy way to obtain a series which had heretofore been scarce in collections. a The specimens found represented both the typical form and Dr. Dyar’s _ variety, hubbardiana. Not only were both forms found, together with all manner os of intergrades, but also forms carrying the hubbardiana idea still further, until only the merest trace of any dark maculation was visible on the ground color. | au this aberration may be known asimmaculata, ab. nov. ats Fe « ba Type Locality: 21 miles north of Gulfport, Mississippi. “8 Dates of Capture: 26th of June, 1921. by Z. Number and Sexes of Types: Holotype ¢, deposited as loan material in the collection of Dr. William Barnes; I paratype, collection of author; 2 para- _ types, collection of Agricultural and Mechanical College, Mississippi. ind ir Mr. Mortimer L. Higgins, Washington, D.C., reports the capture of ap- proximately 100 specimens of the beetle Oxrynemus histrina (Nitidulidae) on a _» single plant of the Stink Horn Fungus (Phallus impudicus). The capture of _ more than one or two specimens on a single plant is very rare, according to ie “Schwarz, Barber and Leng, and the record therefore should be of interest to & oon aa = me Sse ; Ee Ae at “ e- \ wrt ¢ gh Rent race : eee 222 THE CANADIAN ENTOMOLOGIST aie a . NOTES ON THE RELATIONSHIPS INDICATED BY ‘THE VEN NAT c OF THE WINGS OF INSECTS. BY G. C. CRAMPTON, Massachusetts Agricultural College, Amherst, Mass. (Continued from page 216) I have pointed out the close resemblance between the Zoraptera and» Psocids in several papers (Crampton, 1921 and 1922) and I would now defi ly place the Zoraptera in the order Psocida, assigning to the Zorotypoidea rank of suborder, or superfamily. ‘The discussion of the origin of the Zo tera would therefore resolve itself into the question of the origin of the Pso id in general, since what applies to one branch of the Psocids applies to all. A ce parison of the wing of the es show n in Fig. 32 with that of the eS | bi: pedicel off from the common stem ai the Protorthoptera and Prot This view is in harmony with the fact that the wings of certain Psocids are suggestive of the type occurring in some Blattids (compare Fig. 65 with Fig. an A since the Blattids also arose from the common Protorthopteron-Protoblatti stem, and much the same tendencies (i. e. the same genes, determinants, _or fac tors) could enter both the Psocid and Blattid lines of descent, having been herited from their common ancestry. The wings of the Zoraptera are quite — suggestive of a relationship to the Isoptera (and the venation of other Psocids — is rather faintly suggestive of Isopteron affinities) and this also would indie that both Psocids and Isoptera were descended from ancestors very like the P orthoptera (with the Protoblattida.) The resemblance between the wing the Psocid shown in Fig. 32, and that of the Mixotermitoid shown in Fi may be due to their mutual relationship to the Protorthoptera, but it is q possible that the point of origin of the Psocid line of development may | been quite close to the point at which the Mixotermitoid line of developr branched off from their Protorthopteron-like ancestors, and the ree would therefore be due to consanguinity, rather than to “convergence.” marked resemblance between the wings of such Psocids as Zoroty pus and the Embiids - (with the Plecoptera) has been discussed in several papers (Cram ton, 1921 and 1922) and, although both Zorotypus and the Embiids are el related to the Protorthoptera, the resemblance between them is not due solel to their mutual relationship to the Protorthoptera, but is due to a more direc relationship between the Psocids and Embiids (with the Plecoptera), and extremely probable that the line of descent of the Psocids branched off ‘the base of the common Protoblattid-Protorthopteron stem very close to the poin of origin of the common ancestors of the Embiids and Plecoptera ; ane the in sects related to the Blattids (with the Isoptera) “took their origin” this point also. J The Psocids, Mallophaga, Pediculids, Thysanoptera, and Hemipt er rit insects (i. e. Hemiptera and Homoptera) have been grouped in a single supet order, the ‘‘Panhomoptera,” and a study of the venation of the groups in que tion would lend weight to the correctness of this grouping. The Psocids : = ‘4 ee ! ; a: x * : Pas ga BASS a : 7 ney . A ~ ‘ i ae HE CANADIAN ENTOMOLOGIST 223 ly descended from ancestors very like the Protorthoptera, (with their ‘the Isoptera) and the Thysanoptera were apparently descended from an- s resembling the modified descendant of the Protorthoptera shown in Fig. ae as” may be seen by comparing Fig. 33 with Fig. 35. The mutual resemb- lance between the wings of certain Psocids and the Thysanoptera has been dis- he cussed elsewhere (Crampton, 1922) and need not be described here, so that it aS not necessary to do more than call attention to the tact that the relationship ediation of their mutual sSatiicchis to the Protorthoptera (and the Orthop- — ee Tous descendants of the Protorthoptera.) The Pediculids are apparently quite J closely related to the Mallophaga, (and Platypsyllid Coleoptera also) though yoth are wingless groups, and nothing is known of their more direct w inged an- tors, though both were doubtless derived from Psocid-like forms, as is in- “ae ca cated by their general body characters. The Mallophaga in particular are ex- ee emely like Psocids in the character of their head structures, thoracic plates, cic. but they are also astonishingly like the members of the Coleopterous group — =. - Platypsyllidae in certain respects (and they also have certain features in com- Fs m on with the Hemimerid family of the Dermaptera.) If the Psocids, Dermap- # oe and Coleoptera are all to be derived from Protorthopteroid ancestors, this complicated interrelationship of the Mallophaga to all of these orders is readi- comprehensible ; but if this view is inadmissible, the resemblance between ; -Mallophaga and the Hemimerid Dermaptera, for example, must be regard- ; ed as a result of convergent development due to the selective action of similar = er aaa conditions (ectoparasitism. ) “us _ Judging from their general structure, the Thy sanoptera are more closely “a sible. The remarkable parallelism in the venation of a long series of Psocids and. Tomopterous Hemipteroid insects has been discussed in a previous paper (Cramp- , 1922) and the Psocids parallel the Homoptera so closely that it would be very ppropriate to designate the Psocids as ““Parahomoptera” rather than as “Psocop- a,” as is done by certain recent entomologists—especially since all of the Psocop~ he Be. of Psocus) and the diegitiation “Psocoptera” is not at all appropriate for ch Psocids as these, while even Embidopsocus parallels the venation of certain. ieee as was pointed out in the article referred to above. Since the wings of the Psocids parallel those of the Homoptera so re~ “ma eably closely (apparently due to the inheritance of many common genes, de- . imants or factors from a common source) we would expect that if the Pso- ids were derived from ancestors closely related to the common Protorthopteron- Protoblattid stem, the Homoptera would also be derived from ancestors extremely similar to these forms, and indeed, certain Homopterous wings are p ay suggestive of those of certain Protorthoptera, while sucha Homopterous wing as the one shown in Fig. 58 approaches quite closely that of the descendant of 2 common Protorthopteron-Protoblattid stem shown in Fig. 59, and a surpris- are not Psocus-winged (e. g. the wings of Embidopsocus are nothing like — 3¥ is 224 THE CANADIAN ENTOMOLOGIST ingly large number of anatomical features of Hemiptera are “Blattoid.” In fact, it would be quite impossible to derive such a type as the Homopterous wing shown in Fig. 58 from that of Eugereon (Fig. 41) which is supposed to rep- resent the type ancestral to the Homoptera and Hemiptera (Heteroptera), so that it is much more probable that the ancestors of the Homoptera and Hemip- tera were very like the common Protorthoptera-Protoblattid stem, and the com- mon ancestors of the Homoptera and Hemiptera apparently arose at the point where the common stock of the Protorthoptera and Protoblattida began to di- verge from the Palaeodictyoptera, and Eugereon doubtless branched off from the same point, or very near it. Hugereon, however, is more like the Palaeo- dictyoptera (compare figs. 41 and 30), and it possibly may be regarded as_ a specialized Palaeodictyopteron. In stressing the close relationship of the primi- tive Homoptera to the common Protorthopteron-Protoblattid stock, I would not minimize the fact that the Homoptera have also taken over traits from the 7 Palaeodictyoptera into their line of development, but these are to be regarded xe more as persistent features coming up from the common stock which gave rise to both Palaeodictyoptera and the Protorthoptera-Protoblattida—and the Hom- THE CANADIAN ENTOMOLOGIST 227 _ (Figs. 66 and 67) in addition to other features, lie with the Neuroptera (Figs. 69 and 51) and Coleoptera (fig. 72). ‘The evidence of the venation etc., might therefore be taken to indicate that the Hymenoptera, with the Neuroptera and Coleoptera, arose from ancestors whose lines of descent sprang from the point where the common Protorthopteran-Protoblattid stem began to diverge from the Palaeodictyoptera (although no Palaeodictyopterous types which approach the Hymenoptera very closely have yet been found—though the Palaeodicty- optera approach the Hymenoptera’s near relatives, the Neuroptera, very closely), and the line of descent of the Hymenoptera parallels that of the Psocids and other forms descended from the common Protorthopteran-Protoblattid stock on the one side, and the Holometabolous types on the other—with their closest affini- ties with the Holometabola in general, and the Neuroptera and Coleoptera*. in particular. The Coleoptera, Neuroptera and Hymenoptera appear to be the most primitive representatives of the Holometabola, and of these, the Coleoptera are a rather aberrant group not as closely related to the higher Holometabola as the Neuroptera and Hymenoptera are, in certain respects. The ovipositor of such Hymenoptera as X yela is astonishingly like those of the Neuropteron Raphi- dia, but the genitalia of male sawflies are extremely like those of male Mecoptera and Diptera (and somewhat less like those of male Trichoptera and Lepidop- tera). The Hymenoptera are a cerci-bearing group, while the Neuroptera are not, and the larvae of sawflies are rather more suggestive of those of the Trich- optera and Mecoptera which are cerci-bearing groups, so that in these and cer- tain other particulars, the Hymenoptera appear to lead to the Mecopteroid Holo- ~metabola (i. e. the Mecoptera, Diptera, Siphonaptera, Trichoptera and Lepidop- tera), but on the whole. I am somewhat more inclined to regard the Neuroptera as slightly nearer the precursors of the Mecopteroid Holometabola than the Hymenoptera are. The venation of the wings of certain Homoptera is extreme- ly like that of certain Hymenoptera (as has been mentioned before) and the ovi- positor and terminal segments of a Cicada are extremely like those of the Hym- enopteron Sirex, for example; similarly, the wings of the Psocids are very like those of certain sawflies (as was mentioned before) and the general characters. of the Psocids are very suggestive of affinities with the sawflies (and their rela-. tives the Neuroptera). There are also resemblances between the Hymenoptera. and the Embiids (with their relatives the Plecoptera) ; and the Blattids, and their relatives the Isoptera, are apparently extremely like the ancestors of the Hymenoptera. How can we account for this complicated interrelationship in- dicated by many features of the body, and supported by the evidence of the wing-venation as well? ‘The only satisfactory answer so far as I can see, is to admit that all of these forms arose from ancestors occupying a position at or near the point where the common Protorthopteran-Protoblattid stem began to diverge from the Palaeodictyoptera. This view would be supported by the evi- dence of the wing-venation, and would be in harmony with a great number of facts which cannot be explained on any other grounds, so that in the absence of any *The head capsule, neck plates, terga, ovipositor, etc., of certain Hymenoptera are astonishingly like those of certain Neuroptera, while the mouthparts, male genitalia, etc., of the Hymenoptera are more like those of the Coleoptera, and the same is true to some extent, of the wings. 228 THE CANADIAN ENTOMOLOGIST known facts which would tend to controvert it, I feel that we are sate in adopt. ing this view. As was mentioned above, the Mecopteroid Holometabola (i. e. the Mecop tera, Diptera, Siphonaptera, Trichoptera and Lepidoptera) are slightly more closely related to each other than they are to the Neuropteroid Holometabola (1. e. the Hymenoptera, Neuroptera and Coleoptera), and their closest affinities are possibly with the Hymenoptera and Neuroptera, while the Coleoptera are slight- ly further removed from them in many anatomical features. Tillyard, 1919, seems to be inclined to regard the Mecoptera as the nearest living representatives of the types ancestral to the Holometabola in general, but from a study of the general anatomy of the forms in question, I am more inclined to regard the Coleoptera, Neuroptera and even the Hymenoptera, as more primitive (anatomi- cally) than any Mecoptera I have studied, although everyone who has gone in- to the matter at all deeply will readily admit that the Mecoptera have remained as primitive as any of the higher Holometabola (1. e. the Diptera, Lepidoptera, Trichoptera, etc.) in most of their external features at any rate. Tillyard, 1919, would derive the primitive Lepidopterous venation shown in Fig. 54 and the primitive Trichopterous venation shown in Fig. 37, from that of the insect shown in Fig. 52, which he calls a ““Paramecopteron” ; and he would de- rive the primitive Dipterous venation shown in Fig, 61, from that of the insect shown in Fig. 60, which he calls a ““Paratrichopteron.” If the ‘“Paramecoptera” and ‘‘Paratrichoptera” of Tillyard actually represent distinct orders (which I ser- iously doubt) it would be preferable to call the insect shown in Fig. 60 a “Para- mecopteron” (instead of a “Paratrichopteron’’) since its venation is so nearly identical with that of other Mecoptera (such for example as the one shown in Fig. 57) that it does not seem worth while to place it in a distinct order from the Mecoptera, especially since the wings are the only anatomical features known. Similarly, it would be preferable to call the insect shown in Fig. 52 a “Para- trichopteron”’ (instead of a “Paramecopteron”’) if it is to be considered as rep- resenting a distinct order, since its venation parallels that of the Trichopteron shown in Fig. 37, for example. The insect shown in Fig. 52, however, is so much like the insects which Tillyard calls “Protomecoptera” and the primitive Mecopterous types, that I am inclined to regard it also as a primitive representa- tive of the order Mecoptera. If the view that the so-called ‘‘Paramecoptera” and “Paratrichoptera” are merely types of Mecoptera is correct, Tillyard’s deri- vation of the Lepidoptera, Trichoptera, and Diptera is quite in accord with the views of others who have also derived the Lepidoptera, Trichoptera and Diptera from Mecopterous, or Mecoptera-like forbears. I cannot help but feel, however, that the ancestors of the Trichoptera, Lepidoptera, Diptera, etc., were not pure Mecoptera alone, but that the ancestors of some of these at least, were more of the nature of the common ancestors of the Mecoptera and Neuroptera (with the Hymenoptera.) Thus, for example, the primitive type of Lepidopterous wing shown in Fig. 54 might very readily be derived from a type of wing essen- tially like that of the Neuropteron shown in Fig. 51 (and many features of the body in general would bear out this assumption), and certain features of the Diptera, for example, point to a very close relationship between them and the Neuroptera (with the Hymenoptera ) as well as the Mecoptera, and many THE CANADIAN ENTOMOLOGIST 229 other facts would indicate that the ancestors of the higher Holometabola were pre-Mecopterous forms combining in themselves Mecopterous, Hymenopterous, and Neuropterous features, rather than that the ancestors of the higher Holo- metabola were simple Mecoptera. Insects which have retained certain anatomical features in a primitive condition are frequently fairly highly specialized in other anatomical features, and until more is known of the general anatomy of Belmon- tia, it would be unwise to attempt to derive all of the higher Holometabola from the insect whose wing is shown in Fig. 52, especially since a study of the body in general (e. g. head and mouthparts of Micropterygid Lepidoptera, etc.) would point to an ancestry for many of the higher Holometabola in fornis which are fundamentally more primitive than the Mecoptera (to which group I believe that the insect shown in Fig. 52 belongs.) The line of development of the Dip- tera parallels that of the Mecoptera remarkably closely, and the two apparently merge as we trace them back to a common source, and in the same way, the line of development of the Lepidoptera parallels that of the Trichoptera remark- ably closely, and these two lines of descent also appear to merge as we trace them back to their common ancestry. The lines of descent of the higher Holo- metabola’ mentioned above, parallel each other extremely closely, and as we trace them all back to their common source, they are joined by the lines of des- cent of the Hymenoptera, Neuroptera, etc., and all of these apparently lead back to ancestors occupying a position at or near the point where the common stem of the Protorthoptera and Protoblattida began to diverge from the Palaeodicty- optera. Since the lines of development of the Psocids and Homoptera arose at the same point, both of these groups could readily exhibit characters in com- mon with the Lepidoptera and Trichoptera, having inherited the same tenden- cies from their common ancestry—and the Protorthoptera have apparently re- tained more of the characters of this common ancestry than any other group of insects. It would be possible to group the higher Holometabola (i. e. the - Mecoptera, Diptera, Lepidoptera, Trichoptera, etc.) in a superorder (Panme- coptera) distinct from the lower representatives of the Holometabola, but it is preferable to group them all in a single Holometabolous group (Panneuroptera) including the Neuroptera, Coleoptera, etc., as well. The Strepsiptera are a type of Holometabolous insects whose affinities are rather difficult to determine, although the usual view that they are closely re- lated to the Coleoptera is doubtless correct. There are a few points of resem- blance between the wings of the Strepsiptera and those of certain Trichoptera. as may be seen by comparing Fig. 74 with Fig. 73, and in their general anatomy they also exhibit some Hymenopteroid features. Many features of the body (particularly of the abdominal region) of the Hemipteroid insects are extremely suggestive of a relationship to the Strepsiptera, and the wing of the Hemipteroid insects shown in Fig. 75 resembles that of the Strepsipteron shown in Fig. 74 in some respects, while the venation of the Hemipteroid insect shown in Fig. 71 is even more similar to the Strepsipteron shown in Fig. 74. The Psocids also approach the Strepsiptera in certain features. The venation of the Coleopterous wing shown in Fig. 70 is somewhat suggestive of the Strepsiptera (Fig. 74), but the resemblance is not very striking, and the relationship between the Strepsiptera and the Coleoptera is better illustrated by the character of the larvae, and cer- 230 THE CANADIAN ENTOMOLOGIST tain features of the adult anatomy. The wing of the modified descendant of the Protorthopteran-Protoblattid stem shown in Fig. 48 exhibits certain features suggestive of a relationship to the Strepsiptera (Fig. 74), but it is quite possible that any resemblance between the venation of the Strepsiptera and Dermaptera is due to their mutual relationship to the Coleoptera—for I still believe that the Coleoptera are closely related to the Dermaptera as well as to the Neuroptera, since they are anatomically intermediate between the two in their general body structures, although the wings available for comparison do not show this very strikingly. It is very probable that the line of development of the Strepsiptera branched off near the base of the Coleopteron stem, and took over in ‘its line of development certain features inherited from the ancestors of the Coleoptera, which occupied a position close to the common stem of the Protorthoptera and Protoblattids, and were therefore related to the Dermaptera also, since these branched off from the common Protorthopteran stock at the point where the line of development of the Coleoptera arose. Any resemblance between the Strepsiptera and the Hemipteroid insects, is possibly due to the inheritance of common factors from their forbears in or near the common Protorthopteran- Protorblattid stock from which they all arose, although the resemblance between the Strepsiptera and Trichoptera is apparently due to a more direct connection than through the intermediation of the Protorthopteroid forms. The foregoing facts may be briefly summarized as follows. Of the higher insects, the Mecoptera, Diptera, Siphonaptera, Trichoptera and Lepidop- tera are extremely closely related, as are the Neuroptera, Coleoptera (with the Strepsiptera?), and Hymenoptera, and ali of these insects form a natural group of Neuropteroid insects comprising the superorder Panneuroptera (also called Sialomorpha or Sialoformia) corresponding to the Holometabola or Endoptery- gota of entomologists in general.) Of the remaining higher insects, the Psocids (Parahomoptera), which are here regarded as including the Zoraptera as a sub- order or superfamily of the Psocids, the Mallophaga (Lipoptera), and Pedicu-’ lids (Ellipoptera), are quite closely related, and the Hemiptera, with the Homop- tera, are quite closely related to the Thysanoptera, and all of these have been grouped in a Hemipteroid or Psocid superorder called the Panhomoptera (also called the Psocomorpha or Psociformia). The lines of development of these Neuropteroid and Psocid superorders parallel one another so closely (due to the inheritance of many factors in common from their forbears, which occupied a position intermediate between the Protoblattid-Protorthopteran stock and the Palaeodictyoptera) that it has seemed advisable to group them all in a larger subdivision of winged insects called the “Neuropteradelphia,”’ which comprises all of the so-called higher insects. In most of these “higher” insects, the fore wings are larger than the hind ones, and most of them exhibit no marked tenden- cy toward development of an anal fan. Wings held along abdomen when at rest. The Blattids (Palaeoptera) and Mantids (Eudictyoptera) are so closely * related that.they are placed in a single order called the “Dictyoptera” (a term originally applied to the Neuroptera and Odonata) by some recent investigators, and it is largely a matter of personal preference whether they are divided into two orders, or are grouped into one, although if their immediate relatives, the Isoptera, are regarded as a distinct order, they also may be regarded as represent- THE CANADIAN ENTOMOLOGIST 231 ing two distinct orders. The Blattids, Mantids, and Isoptera have been grouped into a Blattoid superorder called the Panisoptera (Blattomorpha or Blattiformia), and the Protoblattids (Propalaeoptera) are also placed-in this superorder provi- sionally. ‘The saltatorial Orthoptera (with which the Grylloblattids may be in- cluded) are extremely closely related to the Phasmids (Cheleutoptera), and, with the Dermaptera, these three types have been grouped into an Orthopteroid superorder called Panorthoptera (Gryllomorpha, or Grylliformia.) The Protor- thoptera are so closely related to the Orthoptera, that they might also be includ- ed in this superorder. If the Protorthoptera are grouped with the mem- bers of the Orthopteroid superorder, and the Protoblattids are grouped with the Blattoid superorder, it is evident that the lines of development of the lowest representatives of the two superorders (1. e. the Protoblattids and Protor- thoptera) quickly merge as we trace their lines of descent a little further back, and this might be taken to indicate that it is preferable to combine the two super- orders into a single Orthopteroid superorder (Panorthoptera.) The Plecoptera and Embiids (Platyptera) are so closely related that they have been grouped in a Plecopteroid superorder called the Panplecoptera (Perlomorpha or Perli- formia), and the fossil Hadentomoids (Proplatyptera) might also be grouped in this superorder, but it is preferable to wait until more is known of these fossil forms before attempting to determine definitely where to place them. The Blat- toid, Orthopteroid and Plecopteroid superorders are so closely related that it is advisable to group them into a division of winged insects called “Orthoptera- delphia.’ Inthe members of this group, the fore wings are usually smaller than the hind wings. There is a tendency toward development of an anal fan, and the wings are capable of being folded along the abdomen. The Ephemerida (Archiptera or Plectoptera) have preserved in their “‘lar- val” stages, certain features which indicate that they are among the most primi- tive of living Pterygota, and with the Odonata (Pseudoneuroptera or Paraneur- optera) they constitute a primitive group of insects which branched off from the Pterygotan stem at an early period, to follow their own paths of spectaliz- ation. Although the Ephemerids are not as closely related to the Odonata as might be expected from certain resemblances to the Thysanoura, which both ex- hibit, the Ephemerids and Odonata may be grouped in the Ephemeroid super- order Panarchiptera (Ephemeromorpha or Ephemeriformia), for the sake of convenience. ‘The Protodonata would also be included in this superorder, since they appear to be merely primitive Odonata, hardly worthy of ordinal rank. The Protephemerida (Protarchiptera) are so closely related to the Ephemerids that they might possibly be.placed in the same superorder with them, but it is preferable to wait until more is known of the fossil forms before attempting to group them definitely. ‘The Palaeodictyoptera were formerly placed in the Eph- emeroid superorder, but it is preferable to place them in a Palaeodictyopteroid superorder (Panpalaeodictyoptera) which would probably also include the Syn- armogoida etc., but so little is known of the fossil forms, that much more in- vestigation is needed before we are able to group them definitely. The Ephemer- oid superorder and the Palaeodictyopteroid superorder constitute the division of winged insects called “Archipteradelphia.’ The wings of the members of this division tend to remain subequal in size, and are usually incapable of being 232 THE CANADIAN ENTOMOLOGIST folded along the body (i. e. are held out from the body when at rest.) True anal fan lacking in practically all of these insects. If we were able to make a detailed study of the immediate precursors (or even the earliest representatives) of the various orders of living insects, they would doubtless exhibit so many features in-common, that it would be ex- tremely difficult to separate them into well defined superorders, and even when we are dealing with living insects alone, the persistence of “synthetic” types, or forms annectant between several orders, makes it very difficult to determine the group with which the forms in question have their closest affinities. The wings of some of the fossil forms sufficiently well preserved for study, combine in themselves so many features common to a large number of recent orders, that when these fossils are “included in any grouping of insects into superorders or larger divisions, these groupings are found to intergrade because of the fact that some of these intermediate fossil forms might as readily be included in one group as another, and it is only when we restrict our consideration to living forms alone, that the superorders and divisions are at all clearly defined. In fact. it would be entirely possible to use a different method of grouping insects than the one proposed above, but the grouping of winged insects into the higher orders ( Neuropteradelphia), lower orders (Orthopteradelphia) and archaic forms (Archipteradelphia) emphasizes the fact that the lines of development of some “hang together for a longer time ” than others do, in “travelling along the road to specialization,’ and I have attempted to give expression to the same idea in grouping the members of these divisions into superorders. ra = aa <2} eee ie s a = Ss a z Be 2 2 oA Fe 3 = 2 = 2Q8484 58.582 alae es #8 €2Aenhee sos F ES Be os Be eae Bases soa 9G 84855 gS BEeEses © yr AAR ODS SS = Resa es = A, eS & S e 2 04 AS ene a & B&B sogssés’ SX 6 ES ERES SS RESHESS 8 B8E7SS S eee\||asee SAnT/SS 8 RRB S ES B/S EA\ YF f Sy : Z : - ‘ARCHAIC PTERYGOTA LOWER PTERYGOTA HIGHER, PTERYGOTA The appended diagrams will serve to illustrate graphically the lines of descent of the principal orders of winged insects, which have been represented in three groups for the sake of simplicity, since if all were given in one figure, there would result a confusing crossing of lines, since the various lines of des- cent converge from three different directions forming a “bush-like” figure repre- sented as though drawn “in three dimensions,” and it is preferable to simplify such a figure by giving its component parts in three sections, as represented in the dia- grams. ‘The “Prodictyoptera” are the common ancestors (or common stem) of the Protorthoptera and Protoblattids; the designation “Prodictyoptera” is used for the sake of breyity in the diagrams. SE Rad Si Raia lee ee ee a aS ale Te ies PES eee ss ‘ THE CANADIAN ENTOMOLOGIST 233 , ABBREVIATIONS. ...Costal vein; Sc. ...Subcostal vein; Rs. ...Radial sector; R,, R., R,, Ry, and R,..Branches of Radial Vein; M,, M.,, M, and M,..Branches of Median vein; Cu. ...Cubital veins; A. ...Anal veins. EXPLANATION OF PLATES. _ Fig. 1. Forewing of fossil Megasecopteron Corydaloides scudderi, redrawn from Handlirsch, 1908. _ Fig.2. Forewing of fossil Orthopteron Locustopsis elegans, redrawn from 3 Handlirsch, 1908. Fig. 3. Forewing of fossil Synarmogoidan Synarmoge ferrarii, redrawn from __ _ Handlirsch, 1920. Fig. 4. Forewing of fossil Sypharopteroidan Sypharoptera pneuma, redrawn from Handlirsch, 1920. Fig. 5. Forewing of fossil Protorthopteron (?) Elcanopsis sydenienis, redrawn : from Tillyard, 1918. Hig. 6. Forewing of Protorthopteron Limopterum ornatum, redrawn from . Handlirsch, 1920. _ Fig. 7. Forewing of fossil Reculoidan Recula parva, redrawn from Handlirsch, a... 1920. a ‘Fig. 8. Forewing of Plecopteron Jsogenus sp., redrawn from Comstock, 1918. . Fig.9. Forewing of fossil Hapalopteroidan Hapaloptera gracilis, redrawn from Handlirsch, 1920. _ Fig. 10. Forewing of fossil Mantid Petromantis rossica, redrawn from Hand- 2 lirsch, 1908. Fig. 11. Forewing of fossil Protorthopteron Gvrophlebia longicollis, redrawn we from Handlirsch, 1920. - _ Fig. 12. Forewing of Isopteron Hodotermes mossambicus redrawn from Hand- lirsch, 1908. : Fig. 13. Forewing of fossil Mixotermitoidan Geroneura wilsoni, redrawn from_ Handlirsch, 1908. _ Fig. 14. Forewing of fossil Mantid Palaeomantis schmidti, redrawn from Hand- = lirsch, 1920. _ Fig. 15."Forewing of fossil Protoblattid Protophasma dumasi, redrawn from a Handlirsch, 1920. pabig: 16. Forewing of fossil Neuropteron (?) Gigantotermes excelsus, redrawn from Handlirsch, 1908. Fig. 17. Forewing of fossil Mixotermitoidan Mixvotermes ligauensis, redrawn from Handlirsch, 1908. ‘Fig. 18. Forewing of Embiid Donaconethis abyssinica, redrawn from Comstock, 1918. . - Fig. 19. Forewing of fossil Protorthopteron Spaniodera ambulans, redrawn from : Handlirsch, 1920. _ Fig. 20. Forewing of fossil Neuropteron Nymphites braueri, redrawn from tee Handlirsch, 1920. _ Fig. 21. Forewing of fossil Hadentomoidan Hadentomum americanum, redrawn | from Handlirsch, 1920. Fig. 22. Forewing of Plecopteron Zelandobius confusus, redrawn from Tillyard. eee 234 THE CANADIAN ENTOMOLOGIST yikes = es ee isch. 1920. en Vig. 24. Hindwing of fossil Protoblattid Protophasma dumast, redrawn fror : ees ne . Fi ‘ig. 25. Forewing of Trichopteron Beracodes minuta, redrawn from ieee 1907. x Tig. 3. Hindwing of Isopteron Mastotermes darwinensis, redrawn from Con stock, 1918. oy Fig. 27. Hindwing of Mantid Wetalleuctra splendida, redrawn from Handles, » 1908. Fig. 28. Forewing of Neuropteron Coniocompsa vesiculigera, redrawn irom Enderlein, 1908. Fig. 29. Hindwing of fossil Protorthopteron Sthenaropoda hho ina fron n Sa. Handlirsch, 1920. oh Fig. 30. Forewing of fossil Palaeodictyopteron Homothetus fossilis, redial from Handlirsch, 1908. - - Fig. 31. Forewing of Psocid Archipsocus brazilianus, redrawn from Enderlein._ Fig. 32. Forewing of Psocid Amphientomum paradoxum, redrawn from Tillyard, ia Pr. 1918. Fig. 33. Forewing of fossil Thysanopteron Palacothrips fossilis, redrawn irom Scudder, 1890. i: Fig. 34. Forewing of fossil Protorthopteron Lepium elongatum, redrawn from eee 1920. eS. Fig. 36. Forewing of Homopteron Dictyophora europaea, redrawn from Hand- 2 lirsch, 1908. Fig. 37. Forewing oi Trichopteron Ryacophila, redrawn from several sources. Fig. 38. Forewing of Trichopteron Chaetopteryx villosa, redrawn from Tian é 1919. Fig. 39. Forewing of Homopteron Bothriocera prosignoretti, redrawn from Met S calf, 1913. 5 Fig. 40. Forewing of Psocid Calopsocus infelix, redrawn from ‘Enderlein, 1903, Fig. 41. Forewing of fossil Protohemipteron Eugereon boeckengi, redrawn rout Handlirsch, 1920. an Fig. 42. Hindwing of Blattid Periplaneta australasiae, redrawn from Handlirseh. 1908. 2 Fig. 43. Hindwing of Blattid Chorisneura nigrifrons, redrawn from Handlirseh, 1908. res Vig. 44. Hindwing of Blattid Diaphana fieberi, redrawn from Handlirsch, 1908. Fig. 45. Hindwing of OpanepteroG Tettix subulata, redrawn from Handlirsch,_ ‘3 1908. ~ 8 Fig. 46. Hindwing of Plecopteron Eusthenia spectabilis. redrawn.from Comstoc 4 1918. a — Tig. 47. Hindwing of Homopteron Myndus, redrawn from Metcalf, 1913. Fig. 48. Hindwing of “an earwig” (Dermapteron) redrawn from Comstock, 1918. Tig. 49. Hindwing of Phasmid XNeroderus kirbyi, redrawn from Handlir 1908. . a THE CANADIAN ENTOMOLOGIST 2355) 0m je 3 Fig. so. Rniaas of fossil Palaeodictyopteron | pi he ees grandeuryi, re- asi. drawn from Handlirsch, 1908. Fig, BY Forewing of Neuropteron Austrosialis ignicollis, redrawn from Tillyard, Bary 2019. | - Fig. 52. Forewing of fossil Mecopteron (?) Belmontia mitchelli, redrawn fronr Bi: r Tillyard, 1919. a. : Fig. 53. Forewing of Neuropteron Protohermes davidi, redrawn from ‘Tillyard, | 1919. =