Vol. XXI January, 1945 No. 1 THE Pan- Pacific Entomologist Published by the Pacific Coast Entomological Society in co-operation with The California Academy of Sciences CONTENTS STEWART, PROFESSIONAL TRAINING IN ENTOMOLOGY 1 VAN DYKE, TWO COLEOPTERA RECENTLY ESTABLISHED IN CALIFORNIA 10 REINHARD, A NEW MUSCOID PARASITE REARED FROM BEETLES IN CALIFORNIA 11 LANGE, AUTOGRAPHA EGENA (GUEN.) A PERIODIC PEST OF BEANS 13 WIND AND CLENCH, NOTES ON THE GENUS THAUMAINA 14 LEECH, ON THREE SPECIES OF AGABUS RECORDED FROM THE STATE OF MONTANA 16 ZIMMERMAN, A NEW JAVANESE OROCHLESIS AND A CHECKLIST OF THE GENUS 17 BLAISDELL, A SYNOPTIC REVIEW OF THE KNOWN SPECIES OF CRYPTOGLOSSA, WITH DESCRIPTION OF A NEW SUBSPECIES 23 TILDEN, NOTES ON REDWOOD CERAMBYCIDS 30 CAMRAS, FURTHER NOTES ON SOME SPECIES OF ZODION 31 TILDEN, NOTES ON SOME MOTHS OF THE FAMILY SATURNIIDAE 32 AMERICAN COMMITTEE ON ENTOMOLOGICAL NOMENCLATURE 33 PROCEEDINGS OF THE PACIFIC COAST ENTOMOLOGICAL SOCIETY.... 34 San Francisco, California 1945 THE PAN-PACIFIC ENTOMOLOGIST E. C. Van Dyke EDITORIAL BOARD E. G. Linsley R. W. L. Potts Associate Editor Editor Assistant Editor R. L. Usinger* G. F. Ferris E. S. Ross* * On military leave R. C. Miller, Treasurer Published quarterly in January, April, July, and October with Society Proceedings appearing in the January number. 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Make checks payable to “Pan-Pacific Ento- mologist.” INSECT BOXES Standard size black insect box with sides of box and cover made of I/ 4 " redwood. The top, bottom and shoulders are of heavy cardboard. Inside dimensions: I 2*4x8 : *4x2% inches. Prices: 60 cents each. Lots of one dozen, 50 cents each. With Masonite bottom, 15 cents extra. With glass top, 50 cents extra. Prices for larger quantities on request. Unit boxes also manufactured Prices on application RAISIN AND THIEBAUT BROS., LTD. 346 First Street, San Francisco, Calif. Entered as second class matter, February 10, 1925, at the postoffice at San Francisco. California, under Act of August 24, 1912. The P an-Pacific Entomologist VOL XXI, No. 1 January, 1945 PROFESSIONAL TRAINING IN ENTOMOLOGY* BY M. A. STEWART University of California, Berkeley From time to time papers have been written and speeches have been delivered concerning the teaching of entomology and com- mittees have been appointed to study the problem of training entomologists. However, little or no action has resulted from these efforts to rationalize the professional education of entomolo- gists and to develop reasonably uniform curricula of high stand- ards comparable to those required of students in the older pro- fessions. Curricula in entomology, even those generally regarded as being among the best, have developed, in very large part at least, more or less under the stimuli of personal interests of prominent faculty members, rather than as the result of careful and exhaustive studies of the legitimate demands upon, and the responsibilities of, the profession of entomology and the conse- quent needs of the student. No whole-hearted and successful at- tempt has been made to standardize, within reasonable limits, the curricula in entomology in the leading universities, which should result ultimately in the adoption of similar programs of study by the smaller and less well endowed institutions. As a consequence of this somewhat laissez faire attitude and failure to develop rigidly professional and more or less uniform curricula, young entomologists graduating from different colleges manifest a remarkable dissimilarity in philosophy of their science, in magnitude and character of information and even in appreciation of their responsibilities and opportunities. The education of students of entomology is a matter of perti- nent concern to teacher upon whom is imposed the responsibil- ity of well equipping these young people for successful and com- petent careers and of anticipating new demands upon entomolo- gists as the scope of the profession expands and as new ap- proaches and new interrelationships with other fields of science develop as a consequence of the normal evolution of the profes- * Presidential address read before the Pacific Coast Entomological Society, January 6, 1945. 2 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 sion. Furthermore, responsibility for maintaining, and increas- ing wherever possible, the standards and competency of profes- sional entomology largely and inevitably rests upon the teachers. Entomological education obviously is of paramount importance to students who are preparing to enter the profession and who rightfully expect their teachers and institutions to equip them well for the career upon which they intend to embark. The training of students of entomology is equally important to ento- mologists who are engaged exclusively in research, regulatory work and other entomological occupations distinct from teaching, since they not only have a natural interest and pride in the pro- fession of which they are members, but also have the responsi- bility of hiring from time to time young entomologists of whom they expect adequate qualifications. Finally, the general public which financially supports entomology is justified in expecting, and even demanding, thoroughly competent entomologists and entomological service of the highest calibre. Thus we see that the education of students of entomology is an extremely perti- nent matter to both professional workers, actual and potential, and to the general public. Particularly must the teachers and the colleges consciously recognize the noblesse oblige that is ines- capably theirs. In order to properly appreciate and evaluate the problem which confronts us, we may ask ourselves certain fundamental questions. The first basic question to answer is what is an entomologist? This question can be answered simply by stating that he is a per- son engaged in the study of the accumulated and accepted knowl- edge of insects and certain other arthropods with reference to the discovery of general truths or the operation of general laws and in adding to this knowledge and making practical applications of it. However, for the more thorough appreciation and evaluation of the problem of professional training in entomology, it is better to erect a more complete definition which recognizes that an ento- mologist is first a biologist, second a zoologist and finally an entomologist. This more basic concept emphasizes the true posi- tion of the entomolgist as a scientist and more clearly indicates the exact nature and magnitude of his specialized training. It should be obvious that failure to accept such a point of view will inevitably result in imposing upon the student restrictions which will narrow the scope of his activities in contributions to JANUARY, 1945] STEWART-PROFESSIONAL TRAINING 3 his field of science. The acceptance of this definition elucidates the extent of specialized education concerned directly with ento- mology, and without regard to the correlated subjects, demanded for true professional status. Extending the definition to comple- tion, one must accept the fact that entomology is so complex as to necessitate subdivision into the specialized fields of system- atics and the several aspects of applied entomology. The second question that must be satisfactorily answered is, what are the responsibilities of entomology as a profession? The most readily apparent reply is that entomology is concerned with the protection of man’s food and clothing, much of his financial investment and his health and that of his domesticated animals from the direct and indirect ravages of arthropods. It is also responsible for the possible furtherance of the effectiveness of insects beneficial to man and his interests. A moment’s reflection presents the fact that entomologists engaged exclusively in what is called, for the sake of convenience, applied entomology are not able to completely discharge their responsibilities alone. Systematists should be working in closest collaboration with such entomologists and supplying them with basic information. Since, by previous definition, entomology in part is also con- cerned with the discovery of general truths and the operation of general laws, responsibility rests upon the profession for train- ing competent workers in taxonomy and encouraging adequate museum facilities and for providing personnel for bionomic and other systematic studies and investigations. These entomologists together with the economic workers effect the compilation of scientific entomological knowledge. A third type of responsibility is met by providing profession- ally trained entomologists for research and service in the insec- ticide industry. It is manifest that in each of these general aspects of ento- mology, which jointly share the professional responsibilities, there are numerous highly developed specialties. At a casual glance it might appear that these specialties are rather distinct and narrowly restricted. Such a concept is entirely erroneous. It is highly urgent that each specialist be sufficiently thoroughly trained in entomology and allied basic subjects and indoctrinated with the broad scientific point of view to have a good working knowledge and sound appreciation of the other fields of ento- mological specialization. The degree of individual competency 4 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 and ethical success of the profession is in direct proportion to the completeness and rationality of the professional training afforded to the student. The preceding statements and analyses are admittedly not new and are elementary, but it is necessary to review the concepts they express and to keep them in mind constantly if the current re- quirements for professional status in entomology are to be criti- cally examined and if a rational approach is to be made to the problem of future improvements in entomological education. Before advancements can be made in the professional training of entomologists, with consequent elevation of standards and greater competency in discharging ethical professional obliga- tions, the faults and deficiencies in prevailing entomological curricula must be recognized. Perhaps the most prominent fault in our curricula is failure to recognize clearly the truly professional status of entomology and to treat it accordingly. It is true that we speak of the pro- fession of entomology, but not with a full and conscious realiza- tion of the significance of the term and recognition of the respon- sibilities membership in it incurs. We have not benefited by the educational experiences of the older professions such as medi- cine, law and chemistry. Failure to profit by the experience and history of older and comparable fields of effort inevitably results in some retardation of progress. Not one of the older professions would accept new students to more or less full status late in their undergraduate years, or omit a rather definite schedule of pre- requisites, or permit widely dissimilar courses of study, or fail to differentiate between pre-professional and professional courses. Departments of instruction in entomology, however, are guilty of all of these educational misdemeanors. Another fault in entomological education is failure to view the field as a whole and as a distinct discipline with necessary ramifications and delimitations. This is a reflection of a weak- ness in recognition and appreciation of the fundamental and scholarly philosophy upon which the profession must be based. Such definitions as are presented earlier in this paper must be accepted and abided by to avoid this serious pitfall of omission. Lack of clearly defined concepts and goals and logical approaches to these goals inhibit, if not prohibit, the attainment of adequate curricula and professional competency. The absence of some reasonable degree of standardization of JANUARY, 1045] STEWART— PROFESSIONAL TRAINING •5 entomological curricula constitutes a serious obstacle in develop- ing consistently entomologists of truly professional calibre. Any- one who has ever been concerned with the teaching of entomol- ogy at the graduate level has been strongly impressed by the great divergencies in the character and magnitude of undergrad- uate curricula in different universities. The obvious result of such a lack of standardization of curricula is that the employer of young entomologists must pay undue attention to the school from which an applicant graduates, and even to the professors under whom he studied, and cannot assume, making exceptions for normal differences in native intelligence, industry and integ- rity, that almost all young graduates in entomology are more or less equally competent professionally. It is deplorable that nearly every department of entomology in the United States fails to differentiate in practice, if not in regulations, between undergraduate or pre-professional and grad- uate or professional courses. One finds a remarkable hodge- podge of courses upon examination of the curriculum for a given semester, or year, of almost any student in entomology. This is, perhaps, particularly true of the graduate student, who frequently is taking concurrently one or more undergraduate courses and courses of the most advanced nature. Because of an apparent inability to recognize that entomology is a distinct discipline and must be treated accordingly, even though it may transect or be intimately correlated with many other fields, or even a group of fields as well exemplified by the relationship between entomology and agriculture per se, there is often indecision as to what subjects should be required in the curriculum and even sometimes vitally essential courses are sac- rificed because of a mistaken conviction that certain other courses should be required. It must be recognized that the first respon- sibility of the department of entomology and the first obligation to the students is that of adequate training for competency in the precise discipline of entomology as a profession and that other courses are of secondary importance, except those which are actually basic to entomology and those which should be reason- ably expected as a part of the cultural education that should be claimed by and demanded of every college graduate. A laxity in the matter of prerequisites has already been sug- gested in the comparison made between departments of ento- mology and departments or schools training students in the older 6 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 professions. The most serious neglect to prerequisites occurs not so much in the courses in entomology as in the proper sequence and correlation of basically important courses outside of those restricted to entomological studies and upon which thorough competency in entomology depends and also of prerequisites to eligibility for admission to graduate school and adequacy for instruction at the graduate level. It is almost the rule, rather than the exception, to see graduate students in entomology pur- suing studies which should have been completed during under- graduate years. It is indeed tragic that such an easily solved problem persists even in our better institutions. Partly because of lack of accurate appreciation and under- standing of the discipline of entomology as a science, partly be- cause of lack of properly organized curricula, partly because of lack of serious study of the needs of the student preparing for a professional career in entomology and partly because of failure on the part of teachers to anticipate probable future demands upon entomology we find, perhaps more frequently than not, a deplorable lack of breadth of training in our entomologists, not only in the more narrowly restricted science of entomology itself but more especially in the basic fields upon which entomology is dependent. It is doubtful if there is a mature entomologist who does not regret that his own training is so conspicuously deficient in certain fundamental things in which he should have been trained as a student. This does not refer necessarily to those fields that have become important recently as a consequence of evolution of the profession, but to those subjects which should have constituted logically a part of his education at the time he was a student. Breadth of training not only in entomology per se, but also in related fields basic to or closely correlated with such professional training are especially urgent for the potential entomological investigator. This is not the place nor the time to present anything that pretends to be a complete or definite curriculum for students who desire to qualify as professional entomologists. Obviously such a curriculum can be erected only from intense and exhaus- tive study and should be the product of a carefully selected group of experienced teachers. However, it is clear that the dif- ference between undergraduate and graduate instruction should be clearly defined and understood. No thoughtful modern en- tomologist would endorse the idea that undergraduate training JANUARY, 1045] STEWART-PROFESSIONAL TRAINING 7 alone qualifies a student as a professional entomologist. The master’s degree has long been, and still is, a perplexing problem to the educator; but we are probably justified in assuming that it satisfies some need in entomological training. It is an irre- futable fact that modern professional demands are such that it is extremely difficult and probably will soon become impossible for the young man or woman to attain full professional status in entomology without first achieving the degree of Doctor of Philosophy or its equivalent. From these facts one may justifi- ably accept some such concept as the following relative to ento- mological education. The undergraduate curriculum may well be considered a pre-professional course, i. e. a pre-entomological course, in which the student is afforded the opportunity to ac- quire adequate preparation for instruction at the graduate level and, at the same time, the cultural education that should be de- manded of every graduate of a reputable college or university. As indicated above, the master’s degree is something of an enigma but might be considered a legitimate and creditable at- tainment for the student who intends to enter regulatory work or to fill some commercial or industrial entomological niche at a sub-professional level. The graduate training directed toward earning the doctorate must be intensive work of a very high scholastic character, fulfilling truly professional criteria. Such a philosophy of instruction demands a carefully planned pro- gressive and coordinated program with a clear understanding of the distinction between the pre-professional character of the undergraduate curriculum and the professional stature of the graduate studies. As previously indicated, no attempt is being made in the present discussion to erect curricula for professional training in entomology; but certain salient and fundamental points may well be mentioned briefly. Manifestly, the student requires as much and as thorough training in entomology as possible. However, the usual tendency to compress the greater part, if not all of this, into the undergraduate years should be avoided. Instead thereof, these courses should be logically and progressively correlated and arranged to extend throughout the four years of pre- professional training and well into the graduate years of study, leaving ample time for the undergraduate student to take ade- quate course work in allied scientific subjects and necessary and desirable cultural courses. Such a recommendation immediately 8 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 raises the problem of the student who decides relatively late in his undergraduate course to enter professionally the field of entomology. There is only one rational and ethical answer to this problem and that is to insist that such students fulfill completely the established requirements regardless of the fact that they may be penalized in many instances by the necessity of devoting one or more additional years to the attainment of a bachelor’s degree. Failure to adhere to such rigid requirements and definite pro- gram can result only in the lowering of the professional stand- ards. The older professions of medicine, law, and chemistry have long ago recognized the necessity and wisdom of such an attitude. During the undergraduate years the student should receive thoroughly adequate training in zoology and botany and in physics and chemistry. However, if studies of the development of the entomological curriculum so indicate, the more advanced required courses in chemistry might be extended into the grad- uate training. Genetics, plant pathology and plant physiology should be required of the pre-professional student. One of the greatest crimes being committed in entomological education to- day is permitting the very frequent occurrence of postponement of studying French and German until the student has matricu- lated in the graduate school. The usual result of this is that the student learns barely enough of these languages to satisfy a lenient examiner and never is able to read French and German accurately and easily. Certainly every student who intends to become a professional entomologist should be required to be- come competent in reading these languages before begininng graduate studies. The entomological investigator has urgent need of at least a working knowledge of statistical analysis. Conse- quently mathematics through statistical analysis should be re- quired; if necessary to prevent the overcrowding of the under- graduate curriculum, the advanced work may be covered during graduate instruction. Elementary economics, at least, might well be required of the student in entomology and competency in English should be demonstrated before admission to graduate standing. Most educators recognize and deplore the astounding ignorance of the fundamentals of the English language mani- fested by a considerable proportion of graduate students in ento- mology. Undeniably the professional entomologist who is unable to speak and write well and accurately is severely handicapped. In addition to the subjects previously mentioned, the undergrad- JANUARY, 1045] STEWART-PROFESSIONAL' TRATNTNG 0 uate student should have as broad a training as at all feasible in the social sceinces and the humanities and thereby enjoy the dig- nity and prestige of the educated man, an inescapable responsibil- ity of every reputable college and university regardless of the specialized curriculum of the individual student. To insure the discharge of this responsibility and the consequent dignity of the entomological profession, the departments of entomology might very well arrange these cultural subjects into logical groups and require each student to satisfy certain minimum requirements in each group. Admittedly such a schedule would curtail the stu- dents’ usual freedom of choice in the matter of electives, but is such a restriction undesirable? It can be strongly argued that closer direction of the undergraduate’s selection of elective sub- jects is highly desirable because of his own necessarily limited ability to evaluate courses and to appreciate problems of subject correlations and the necessity of broad professional and cultural perspectives. Furthermore, closer regulation of electives will re- sult in the student profiting more from the considered judgment of the mature scholar. Some will wonder, and even challenge, why courses in agri- culture per se are omitted from the general consideration of an entomological curriculum as presented above. The most impor- tant reason for this omission is that an entirely adequate pro- gram for the training of students in entomology up to the truly professional level does not permit, in the space of seven or eight years of college study, the inclusion of much in the way of strictly agricultural subjects without sacrificing other courses of urgent and greater importance to entomology as a distinct profession. Another reason for this point of view is that agricultural prac- tices are constantly developing and changing and what the stu- dent learns in college of these things is frequently out-dated within a period of very few years; such a condition does not justify overcrowding or infringing upon an already heavily bur- dened and exacting curriculum. Finally, the actual need of courses in agriculture is questionable since experience has shown that the fundamentals and the practical details necessary to the entomologist in his investigations in agricultural entomology and his recommendations for insect control are easily and quickly acquired in the course of early professional duties through con- ferences with and advice of cooperating agricultural specialists. Thus far no mention has been made of the graduate student’s 10 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 research and dissertation. It is sufficient here to point out that the fundamental purpose of this aspect of graduate requirements is to acquaint the student, on a broad plane, with research meth- ods and to afford him an opportunity to demonstrate his ability to organize and conduct research and to properly and adequately handle the results obtained from such investigations. If the teacher recognizes the implications contained in such a concept of the dissertation, he will immediately appreciate the serious thought that must be given to the selection of a research problem for the graduate student and the careful and discreet guidance that he must give to the student. Too frequently, the research problem is either carelessly or thoughtlessly chosen or is selected to further the professor’s own research, either of which should disqualify the professor for the privilege and responsibility of directing graduate students. The problems presented in this discussion are urgent and of major importance if the scholarly and scientific heritage of the field of entomology is to be preserved and is to serve as a source of inspiration to future entomologists as it has been to those of the recent past and if entomology is to deserve the dignity of a professional status. TWO COLEOPTERA RECENTLY ESTABLISHED IN SOUTHERN CALIFORNIA C onoderus laurentii (Guer.) This West Indian elater was ac- cidentally introduced into Florida and Alabama at least forty years ago and is now well established there. On August 2, 1938, I received a specimen of the same from E. Herald, taken on his lawn in Los Angeles and on October 15, 1944, another specimen collected by Mrs. Barbara Prendergast, at Hollywood. Accord- ing to Prof. Ralph H. Smith, this species is now fairly well es- tablished in lawns in various places in southern California. Staphylinus ( Goerius ) olens Mull. A common European spe- cies, generally listed as Ocypus olens Mull, in most insect works, was first noticed at Hollywood, April 16, 1936, and West Los Angeles in November, 1940, and more recently found in abund- ance in various places near the Campus of the University of California at Westwood, Los Angeles, according to Prof. R. H. Smith. These are, I believe, the first records for this species in this country. Fortunately it is a beneficial insect. — Edwin C. Van Dyke. JANUARY 1945] MINHARD — NEW MUSCOID PARASITE 11 A NEW MUSCOID PARASITE REARED FROM BEETLES IN CALIFORNIA 1 (Diptera) BY H. J. REINHARD College Station, Texas The species described below is an interesting addition to the list of Sarcophaga forms whose biologic relationships with beetle hosts have been definitely established through rearings. I am indebted to Dr. E Gorton Linsley for the privilege of study- ing the present material, all reared from Thyce sanfordi Casey. Types of the new species are deposited in the California Academy of Sciences collection. Sarcophaga thyceae Reinhard, new species Related to S. ( Acanthodotheca ) prohibita Aldrich, but at once distinguished by the much wider front, larger palpi, pres- ence of orbitals and outer verticals in the female ; also, there are well marked genitalic differences in both sexes. Female. Front at vertex 0.32 of head width (average of four specimens, 0.33; 0.31; 0.30; 0.32), widening but slightly toward antennal base; parafrontals and parafacials usually silvery gray, latter with one or more rows of black hairs on outer margin ex- tending to lower extremity; frontal vitta black, much wider than parafrontal on entire length; inner and outer verticals well de- veloped, erect; proclinate orbitals two pairs; ocellars moderately large; frontal rows strongly divergent beneath base of antennae and extending to or below middle of second segment; epistoma short, equal clypeal width and slightly bowed forward from plane of same; vibrissae stout, on oral margin; facial ridges bearing a few bristly hairs on lower extremity; antennae mostly black, third segment barely twice length of second and reaching almost to oral margin; arista longer than antenna, long plumose to middle or slightly beyond; cheek gray pollinose, nearly two-fifths eye height; palpi yellow, slender nearly to middle thence strongly swollen and tapering apically to pointed tip; proboscis short; back of head gray pollinose, moderately clothed with pale pile and two rows of black bristly hairs above. Thorax gray pollinose with the usual 3-5 black dorsal vittae. Chaetotaxy: acrostical 3,1 (rather weak except prescutellar pair) ; 1 Contribution No. 873, Division of Entomology, Texas Agricultural Experi- ment Station. 12 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 dorsocentral 3,3; intraalar 3 (front small); posthumeral 1; hu- meral 3; notopleural 4; postalar 2; sternopleural 3; scutellum with 2 lateral, 0 apical and 1 preapical pair; prosternum bare; sides of postnotum beneath calypters. setose; propleura usually bare but sometimes with a few setae on anterior edge; calypters opaque, white. Abdomen slightly elongated, black, gray pollinose and strongly tessellated above with a constant median black vitta extending almost to hind margin of fourth segment, which is reddish in ground color; all dorsal bristles reduced in size to weak or barely differentiated bristly hairs; one median marginal pair on third segment and a marginal row on fourth; genitalia red; first seg- ment bare and shiny above, transversely grooved shortly before hind margin and more deeply so at sides, the latter somewhat swollen or inflated between groove and basal margin, hind edge of segment with a fringe of fine black hairs; anal orifice rather large and strongly arched above; larvipositor retracted, blunt-tipped, with the lateral apical lobes clothed with short black hairs. Legs black, moderately stout; mid tibia with two bristles on outer front side near middle; claws and pulvilli normal in size. Wings gray hyaline; first vein bare, third setulose halfway or more to small cross vein; first posterior cell open well before wing tip; costal spine nearly one-half length of small cross vein; epau- let black, subepaulet pale yellow. Male. Front at vertex 0.22 of head width (average of four specimens, 0.21; 0.22; 0.23; 0.23), narrowed before triangle thence widening rapidly to antennae; parafrontals and parafacials silvery with a decided yellow tinge; orbitals and outer verticals absent; palpi ordinary in size and but slightly thickened apically; cheek about one-third eye height. Thoracic chaetotaxy as in female but good-sized decussate apical scutellars present and the bristles on abdomen normal in size; third segment bearing a median marginal pair and a marginal row of 8 to 10 on anal segment. Hypopygium reddish yellow; first segment dusted with pollen and slightly in- fuscated dorsally, with about 8 slender bristles on hind margin; second segment subglobose, clothed with longish erect black hairs on entire shiny surface above; forceps moderately long, dark brown, in profile rather thin and gently bowed, beset with minute stubby spines apically on hind side; in rear view the forceps are flat and rather broad, divided except at base but not divergent, with apex of each prong obliquely narrowed outwardly; penis with a rather short yellowish basal segment; second segment longer, shiny brown, convex behind and widened distally with each lateral extremity terminating in a minute bowed hook, the apex between latter broadly and deeply emarginate bearing a pair of recurved divergent hooks on hind side and a rather large subquadrate lobe in front, latter flattened or slightly concave on apical surface with the ventral edge terminating in a curved lip, which bears a small roundish transparent flap on either side; claspers tapered to January, 1045] LANGE — AUTOGRAPH A EGENA 13 pointed curved tips, hind pair moderately long, front ones short with broad base bearing several long hairs on hind side; acces- sory plate longer than wide, narrowed tip with sparse long hairs; lobes of fifth sternite thickly covered with black spiny hairs and each bearing a shiny concave pad on inner margin near base. Middle femur with comb; hind tibiae not villous; claws and pul- villi longer than last tarsal segment. Length, 8.5 - 11 mm. Holotype female (No. 5443, Mus. Calif. Acad. Sci., Ent.), and allotype male (No. 5444), San Jose, California, July 25, 1941, and August 1, 1942, reared from Thyce sanfordi Csy. (E. G. Linsley and L. M. Smith). Paratypes: 4 males and 8 females, same data as type. AuTOGRAPHA EGENA (GUEN.) A PERIODIC PEST OF BEANS IN California Autographa egena (Guen.) (Lepidoptera: Phalaenidae) was observed during October, 1943, at Salinas, Monterey County, California, where the caterpillars fed on the leaves and green pods and seeds of beans, especially the pole types. In certain instances the damage was so severe that almost complete defoli- ation of the plants resulted. During July, 1936, a previous out- break of this insect was noted at Half Moon Bay, California, at which time the caterpillars damaged a white Kentucky Wonder pole bean. At Salinas the larvae pupated during November, rolling the leaves and transforming within a silken cocoon. Adults emerged in December, 1943, and again in May, 1944. Several generations occur during a single year. Four parasites of the larvae were found. A count made of caterpillars collected during August, 1943, indicated the relative per cent of parasit- ism as follows: Copidosoma probably truncatellum (Dalm.) (det. A. B. Gahan), 14 per cent; “Amblyteles” montarms (Cr.) (det. H. K. Townes), 1 per cent; “Ephialtes” sanguineipes (Cr.) (det. H. K. Townes), 1 per cent; and Chaetogaedia monticola (Big.) (det. M. T. James), 3 per cent. In addition to these para- sites a fungus killed 2 per cent of the larvae and 2 per cent failed to emerge for unknown reasons. The adult moth was kindly determined by Carl Heinrich. — W. Harry Lange, Jr. 14 THE PAN-PACIFIC ENTOMOLOGIST [yOL. XXI, NO. 1 NOTES ON THE GENUS THAUMAINA (Lepidoptera: Lycaenidae) BY R. G. WIND 1 AND H. K. CLENCH 2 t . 1 | The monotypic genus Thaumaina was erected in 1908 by G. T. Bethune -Baker for the new species described under the name uranothauma. It is a very distinct genus, bearing a pat- tern relationship to the genus Uranothauma Butler (P. Z. S. 1895, p. 631), hence the specific name. It remains one of the peculiar developments of the vast island of New Guinea. Genus Thaumaina Bethune-Baker Bethune-Baker, 1908, P. Z. S. 1908, p. 116. Genotype. Thaumaina uranothauma B.-B. The single species thus far known appears to be restricted to eastern New Guinea, where it is broken up into two races, one of which is described herein as new. It is evidently a highland butterfly, and does not appear to be very common. The typical form was described ( loc . cit. and pi. 9, figs. 8, 9) from the Angabunga River, a tributary of the St. Joseph River, which empties on the south coast of eastern New Guinea. On the opposite side of the Owen Stanley Mountains occurs a race of this species. Karl Jordan (1930, Proc. Ent. Soc. London, 5:60, pi. 3, f. 10) has figured a female of this subspecies that agrees well with the allotype described below. This specimen originated on the Edie River, west side of Herzog Mountains, eastern New Guinea. Two males were taken with it, but were not figured. Thaumaina uranothauma deliciosa Wind and Clench, new subspecies Thaumaina uranothauma : Jordan, loc. cit. Upper side: Male. Fore wing blackish brown with a bright purplish blue patch in the base, from inner margin up to include the lower half of the cell, and extending two-thirds outwards on inner margin. Hind wing with the outer half (nearly two-thirds the area) of the wing brownish black. Costa inside white, darker outwardly. Re- 1 Berkeley, California. 2 Cambridge, Massachusetts. JANUARY, 1945] WIND AND CLENCH — THAUMAINA 15 maining portion of the wing (save for a narrow inner marginal border) purplish blue. Fringe of both wings black and white checked. Female. Fore wing similar to that of the male, but with the blue changed to white and a little more extensive, and with a dark bar extending down over the cell-end from the costa. Hind wing with a broad (outer third of the wing) black-brown border. The remaining area is white with pale blue scaling over the inner marginal part. Extreme base black-brown. Veins in the white area lightly scaled with black-brown. Fringe as in the male. Underside : Male. Fore wing with the ground color white. A dark ban scal- loped marginal border, behind which is a row of alternately dis- located hollow quadrate spots. This row extends from costa to Cu 2 , while the marginal border proceeds all the way to the inner margin. In the M 3 -Cui and Cui-Cu 2 interspaces the border and row of spots touch. On the costa is a triangular, black-brown spot, its apex narrowly produced to cover the cell-end. In the base is a long bar, parallel to the costa, and with a connection to it at its outer extremity. Hind wing with the dark tan scalloped border as in the fore wing, but with the Cui-Cu 2 lunule enclosing a black spot. In the Mi-Cm interspace is a series of connected, jet-black spots, touching the marginal border. In the interspaces from Cu a to the inner margin are three more heavy spots, decreasing to- wards the latter in depth. Base of wing with an irregular black spot. A black, heavy dash, faintly white within, closes the cell. On the costa, almost on the outer angle, is a hollow, nearly circu- lar spot, and one-third from the base is a couplet of similar, though smaller, spots. These markings are all crowded, and almost all appear quite confluent. Female. Similar to the male, save that the post-discal row of spots on the fore wing is larger and more confluent, and as a consequence, less dislocated. Length of fore wing : Male and female, 11.5 mm. Holotype male, Wau, Morobe District, New Guinea, Janu- ary 30, 1933 (H. Stevens). Allotype, female, Mt. Misin, 6400 feet, Morobe District, New Guinea, May 2, 1932 (H. Stevens) . Paratypes, two males, same locality and date. Holotype and allotype in the Museum of Comparative Zoology. One paratype in collection of each author. Remarks. This subspecies appears to differ in a number of respects from the description and figure of Bethune -Baker. The black border of the male appears a little heavier on the fore wing, and even more so on the hind wing. On the latter there is no indication of the white spot mentioned and illustrated by him. In the female there are no white spots in the dark border 16 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 of the fore wing (two were described, and both show up well in the figure), and the cell is closed by a dark streak running from the costa, absent in the description and figure of the typical sub- species. In the hind wing the pale blue scaling of deliciosa is not mentioned by Bethune-Baker, or depicted in his figure. The underside appears to be similar, but perhaps with the spots slightly larger. ON THREE SPECIES OF AGABUS RECORDED FROM THE STATE OF MONTANA 1 (Coleoptera, Dytiscidae) BY HUGH B. LEECH Vernon, British Columbia The inclusion of Agabus confertus Le Conte (det. H. C. Fall) in Mank’s list of the Coleoptera of Glacier Park (1934, p. 75) was for some years a puzzle to me, as all specimens I had seen were from much nearer the coast. Through the kindness of Miss Mank I examined both Montana specimens on May 3, 1939, and found them to be Agabus erichsonii G. & H., a species of similar facies. A. confertus may yet be found in Montana for I have seen one taken at Boise, Idaho, June 15, 1941, by Borys Malkin. In September 1941, Dr. Harlow B. Mills was so kind as to allow me to examine certain of the Agabus reported upon by Hatch (1933, p. 10). The A. seriatus (Say) of Hatch are all the subspecies inter sectus (Crotch) of Leech 1942. The series of “obliteratus Lee.” proved to be composite; two of the specimens from Bozeman are strigulosus (Crotch) ; the others, as well as those from Shields River and Bitter Root Valley are A . nectris Leech. References Hatch, Melville H.,. 1933, Records of Coleoptera from Montana, Canad. Ent. 65(1): 5-15. Leech, Hugh B„ 1942, New or insufficiently known Nearctic species and subspecies of Agabus (Coleoptera, Dytiscidae), Canad. Ent. 74(7) :125-136, 1 pi. (= p. 127). Mank, Edith W., 1934, The Coleoptera of Glacier Park, Montana, Canad. Ent., 66(4):73-81. 1 Contribution No. 2322, Division of Entomology, Science Service Department of Agriculture, Ottawa, Ontario. JANUARY 1945] ZIMMERMAN — OROCHLESIS 17 A NEW JAVANESE OROCHLESIS AND A CHECKLIST OF THE GENUS (Coleoptera, Curculionidae) BY ELWOOD C. ZIMMERMAN Bernice P. Bishop Museum, Honolulu Among some specimens of insects collected in Java by Mrs. M. E. Walsh, there is a pair of weevils which represent a distinct new species of the cryptorhynchine genus Orochlesis Pascoe, 1871. There have been no Orochlesis reported from Java here- tofore, and this paper is written principally to record the addi- tional geographical data supplied by the new species. With the description of another new species, the number of known Orochlesis is raised to 24. A new checklist of the de- scribed species of the genus, arranged by locality from east to west, follows: 1. Orochlesis lunata Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :5, figs. 1, a, c; 2, a; 3, f. 1936, same journal, 12(23) :47. Tahiti, Society Islands. 2. Orochlesis gibbera Zimmerman, 1936, same journal, 12(1) :7, figs. 1, b (1 ) ; 2, b; 3, e. 1936, same journal, 12(23) : 47. Raiatea, Society Islands. 3. Orochlesis nigrofasciata Marshall, 1921, Proc. Hawaiian Ent. Soc., 4(3) :593. Samoa. 4. Orochlesis vitticollis Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :9, figs. 2, d; 3, c. 1936, same journal, 12 ( 22 ) : 6 . Viti Levu, Fiji. 5. Orochlesis bryani Zimmerman, 1936, same journal, 12(1) : 11, figs. 2, e; 3, b. 1936, same journal, 12(22) :6. Viti Levu; Taveuni, Fiji. 6. Orochlesis nigra Zimmerman, 1936, same journal, 12(1) :12, figs. 2, f; 3, a. 1936, same journal, 12(22) :8, fig. 1, d. Viti Levu, Fiji. 7. Orochlesis angulata Zimmerman, 1936, same journal, 12(22) :4, fig*. 1, b. Viti Levu, Fiji. 8. Orochlesis bella Zimmerman, 1936, same reference, p. 5, fig. 1, a. Vanua Levu, Fiji. 18 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 9. Orochlesis eluta Zimmerman, 1936, same reference, p. 7, fig. 1, e. “Fiji”. 10. Orochlesis tessellata Zimmerman, 1936, same reference, p. 8, fig. 1 , c. Ovalau, Fiji. 11. Orochlesis ater Zimmerman, 1939, Pan-Pac. Ent., 15(2) : 57. Viti Levu; Taveuni, Fiji. 12. Orochlesis conspersa Zimmerman, 1938, Proc. Hawaiian Ent. Soc., 10(1) :165. “Solomon Islands”. 13. Orochlesis posticalis (Lea) Lea, 1913, Trans. Royal Soc. South Austr., 37:327. Queenslandica posticalis Lea, 1903, Proc. Linn. Soc. New South Wales, 28:665. Zimmerman, 1936, Occasional Papers Bishop Mu- seum, 12(1) :13. Queensland, Australia. 14. Orochlesis delta Lea, 1913, Trans. Royal Soc. South Austr., 37:328. Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :13. Queensland, Australia. 15. Orochlesis personata (Pascoe) Lea, 1913, Trans. Royal Soc. South Austr., 37:328. Acacallis personata Pascoe, 1883, Ann. Mag. Nat. Hist., (5)12:96. Queenslandica munda Lea, 1903, Proc. Linn. Soc. New South Wales, 28:666. Zimmerman, 1936, Occasional Papers Bishop Mu- seum, 12(1) :14. Queensland, Australia. 16. Orochlesis cornuta Zimmerman, 1936, same reference, p. 14, figs. 1, b; 2, c; 2, d. Queensland, Australia. 17. Orochlesis flesina Pascoe, 1871, Jour. Linn. Soc. London, Zool., 11:195. Zimmerman, 1936, Occasional Papers Bishop Museum, 12:17. Aru Islands (south of Papua). 18. Orochlesis maculosa Pascoe, 1874, Jour. Linn. Soc. London, Zool., 12:40. Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :17. Salwatty Island (off the western tip of New Guinea). 19. Orochlesis solea Pascoe, 1871, Jour. Linn. Soc. London, Zool., 11:195. Marshall, 1921, Proc. Hawaiian Ent. Soc., 4(3) :593- 594. Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :17. Batchian, Moluccas. 20. Orochlesis annularis Pascoe, 1871, Jour. Linn. Soc. London, Zool., 11:194, pi. 8, figs. 2, 2a. Lea, 1913, Trans. Royal Soc. South Austr., 37:327. Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :17. JANUARY, 1045] ZIMMERMAN— OROCHLESIS 10 New Guinea; Yule Island (Gulf of Papua) ; Dorey and Batch- ian Islands, Moluccas; Makassar, Celebes; Luzon, Philippines; Penang Island, Malacca Straits. 21. Orochlesis picticollis Zimmerman, new species. Java. 22. Orochlesis anteplagiata Heller, 1934, Wiener Ent. Zeit., 48:104. Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) :18. Formosa. 23. Orochlesis takaosanus Kono, 1932, Insecta Matsumurana, 6(4):178, pi. 6, fig. 8. Zimmerman, 1936, Occasional Papers Bishop Museum, 12(1) : 18. Honshu, Japan. 24. Orochlesis meshimensis Kono, 1937, Insecta Matsumurana, 11:129. Meshima (Danjo), Japan. Orochlesis picticollis Zimmerman, new species (figs. 1-3) Color', derm piceous to shiny black; scaling very dense, mostly completely or almost completely concealing derm, ground color basically mouse^gray, the scales mostly with a slight, but distinct, iridescence; head and base of rostrum with brown scales with paler patches on either side of median line at base and at inner dorsal parts of eyes; pronotum with disk largely occupied by a large, conspicuous, subcircular, variable patch of dark brown or velvety black scales extending from base to beyond sub apical con- striction, in its emphasized form very prominent and strongly con- trasting with the paler background scaling, scaling on sides from above coxae to dorso-lateral margins more brownish than on dorsum; elytra almost uniformly mouse-gray with a yellowish brown cast without any distinct maculae, setae darker than back- ground; leg scaling similar in color to that of sides of pronotum and elytra, not spotted nor banded; scales on sternum and first two abdominal segments pale yellowish brown, those on ventrite 2 mostly slightly darker than those on metasternum; ventrites 3, 4 and 5 with a conspicuous patch of dense pale yellowish brown scales on either side, but with dark scales elsewhere. Head with derm completely concealed by squamae, the scales large, mostly directed dorsad; with stout, erect, clavate setae along inner margins of eyes and on either side of median line of crown; most scales on interocular area and anterior part of crown slant- ing, slightly sub-erect; narrowest part of interocular area slightly narrower than base of rostrum; crown slightly flattened (best seen when viewed from side). Rostrum only slightly arcuate, almost straight in female; densely squamose at base in female, to middle in male; closely punctate and finely reticulate to beyond basal scaling in female, but with denser punctures and coarsely reticulate in male. 20 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 Antennae (described from left antenna removed from female) with the sinuous, clavate scape about as long as funicular seg- ments 1-4 inclusive, about as broad at its widest part as funicular segment 7; funiculus with segment 1 nearly as. long as 2 plus 3, segment 2 not quite as long as three following segments together, segments 3 to 7 successively broader; club almost as long as funi- cular segments 3 to 7 inclusive. Pronotum broadest near base, about two-fifths or one-third broader than long (measurements of specimens described as fol- lows: male, 48 units wide to 33 long; female, 57 units wide to 37 long) ; base sinuate; strongly arcuate on sides from base to beyond middle and then strongly constricted, thence pointedly narrowed to apex; the constriction broadly and deeply continued across dorsum; distance across dorsum at transverse constriction about one-half basal breadth; longitudinal dorsal contour with area be- hind transverse depression on a higher plane than area in front of depression; extreme apex (viewed from side) thick, about one- half as thick as breadth of a fore tibia; the closely punctate derm completely concealed by very dense, unusually large, broad, fan-shaped, strongly imbricated, anteriorly directed scales; most scales in dark discal macula erect or sub-erect; with stout, erect, clavate setae in the dark discal macula, along either side of median line beyond transverse depression to apex, more numerous on either side of apex where the scales and setae produce the margin into a blunt point on either side of apex, scattered along latero- apical margin back to lateral constriction, and with a slightly condensed group of setae tending to form a feeble fascicle mesad of the true lateral margin at hind margin of transverse constric- tion, and with scattered setae from there to base. Scutellum subquadrate or subrectangular, bare, coarsely reticu- late, dull. Elytra about two-thirds as broad as long, slightly more than two and one-half times as long as pronotum (measured from side from humeri to apex) ; base distinctly sinuate, only as broad at humeri as base of prothorax, broadest behind middle, and there but hardly broader than base, almost straight on sides to beyond middle; longitudinal dorsal contour rising abruptly from shortly behind base to reach a distinctly higher elevation thaji that of base of pronotum; derm completely concealed by dense scaling similar to that on pronotum, but with a few polished, setiferous granules showing through in basal third of interval 1 or less dis- tinctly on intervals 3 and 5 also; alternate intervals slightly more convex than even-numbered ones, and each odd-numbered interval bearing a row of slanting, stout, clavate setae; interval 1 with a low subbasal callosity on which the setae and granules are more abundant, intervals 3 and 5 with a tendency toward having less conspicuous subbasal callosities (none of the callosities are out- standing and those on the fifth intervals may be indistinct or ob- JANUARY, 1045] ZIMMERMAN— OROCIILESIS 21 solete) ; striae showing narrowly through the scaling, punctures indicated through the scaling, but none completely exposed. Legs all densely clothed with large, imbricated scales which conceal derm ; femora and tibiae with stout, clavate, scattered setae which are most abundant along dorsal edges; anterior femora with a sharp carina extending almost entire length of ventral sulcus thus dividing it into subequal parts, with a few scales on outer side of carina, other femora deeply sulcate from base to apex but with- out any such carinae; tibiae broad, greatest breadth of hind pair one-third of greatest length excluding uncus, greatly compressed, outer margins knife-edged but squamose, carinate only along either side of inner edge, inner edge straight, outer edge arcuate, that of hind pair subangulate, with a patch of black setae on outer side at base of the strong unci, conspicuous on two posterior pairs Explanation of Figures Fig. 1, lateral outlines of Orochlesis jncticollis Zimmerman with dark prothoracic macula and type of squamae indicated. Fig. 2, contours of head, prothorax and elytra from side. Fig. 3, outlines of a hind tibia. (Drawings from female allotype.) of tibiae but less conspicuous on anterior pair, the long yellow setae arising from inner apical angle extending to apex of' uncus; tarsi with numerous, slender setae and setiform squamae, anterior pair with segment 1 as long as 2 plus one-half of 3, 2 about as long as median length of 3, 3 about one-third broader than long and as broad as 1, about as long as 1. Sternum , with mesosternal receptacle strongly protuberant, ex- tended to a level slightly ventrad of that of mesocoxae, its outer walls densely clothed with large squamae, hind wall from meta- sternum to aperture about one-half as long as median line of meta- sternum, aperture about on a line with anterior edges of meso- 22 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 coxae; all coxae densely squamose; metastemum flattened in fe- male, concave in male, densely clothed with very large, broad, partially imbricated, ovate scales, which almost entirely conceal the derm, with large, deep, angular, bare fovea situated on caudal one-third of median line, posterior margin broadly emarginate, shortest distance between mid and hind coxae about seven-tenths as long a& longitudinal chord of a mesocoxa or about as long as ventrite 5; pleura densely squamose. Abdomen with ventrite 1 broadly concave in both sexes, but with longitudinal contour less even in female, coarsely reticulate, the punctures on disk bearing very large, rounded or subcordate scales which conceal most of the derm but are mostly not imbri- cated, most scales just) touching or narrowly separated from their neighbors, scales much smaller at sides where femora contact the ventrite, length along median line about as long as ventrites 2 plus 3, hind margin broadly emarginate from sides to middle; ventrite 2 as long as ventrite 3 plus 4 plus about one-half of 5, clothed with large scales similar to those on ventrite 1, but denser and with more scales overlapping; ventrites 3 and 4 with slender, anteriorly directed setae along anterior edge, with a very dense patch of large, erect or sub-erect, imbricated, pale scales at each end and the space between with erect but strongly and conspicuously re- curved dark scales in one or partially two rows; ventrite 5 with vestiture similar to that on 3 and 4 but with entire disk filled with the dark erect squamae. Length: 5.5-6.25 mm.; breadth: 2.75-3.5 mm. Holotype male and allotype female collected by Mrs. M. E. Walsh at Manddalawangi, Mt. Geda, West Java, elevation 4,000 feet, May, 1939; in the type collection of Bishop Museum. This species is not closely allied to any of the other species of the genus known to me. The large black prothoracic macula is broken down in the male holotype, but it is very conspicuous in the female allotype on which it somewhat resembles a broad black tear-drop. It is almost circular in form, but the anterior part is extended forward to make a tear-drop or inverted sub- heart-shaped macula. The setae on the alternate elytral intervals appear as rows of small black dots to the unaided eyes. The scales are unusually large and dense overall. January, 1045] BLAISDELL— CRYPTOGLOSSA 23 SYNOPTIC REVIEW OF THE KNOWN SPECIES OF CRYP- TOGLOSSA SOLIER, WITH DESCRIPTION OF A NEW SUBSPECIES (Coleoptera: Tenebrionidae) BY FRANK E. BLAISDELL, SR. Associate in Research, California Academy of Sciences, San Francisco The species under consideration, inhabit the arid areas of the Sonoran Region of the south-western United States, northern Mexico and Lower California. They are as follows: Genus Cryptoglossa Sober Asbolus LeConte, 1851, Annals Lyc., N. Y., p. 129. Cryptoglossa Sober, 1836, Soc. Ent. Fr., 5, p. 680; Lacordaire, 1859, Genera Coleopt., 5, p. 135; Horn, 1870, Revis. Tenebr., Amer. Philos. Soc., 14, p. 278 and 280; LeConte and Horn, 1883, Class. Coleopt. N. Amer. (Smiths. Miscel. Coll. 507), p. 368. Head large and deflexed, epistomal apex scarcely truncate to feebly arcuate Mentum large and rounded, apex slightly emargi- nate at middle; buccal fissure wide, palpi not dilated. Antennae strongly compressed, eleventh segment short and transverse, slightly received into the tenth. Prosternum produced posteriorly, broad and rounded at apex. Legs stout, tarsi clothed with long ferruginous setae beneath; first segment of the posterior tarsi longest. Cryptoglossa bicostata Solier Zopherus bicostatus Sober, Dupont collection (PI. 24, figs. 11-13). Cryptoglossa bicostata Solier, 1836, Ann. Soc. Ent. Fr., 5, p. 681, t. 24, f. 11^13; Cast. Hist. Nat. II, 1840, p. 191. A Mexican species described from a unique specimen, resem- bling the common Sonoran species ( verrucosa Lee.) in form and tuberculate elytra, except that the fifth interval of each elytron is convex, more or less prominent and costate from the elytral base to about posterior third of the length (fig. 13), and there changing to tubercles. In the type and only known specimen, the distal segments of both antennae are missing, the character of the eleventh or terminal segment being unknown. This fact leaves the correctness of the determination open to doubt. 24 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXI, NO, 1 In Cryptoglossa the eleventh antennal segment is short, trans- verse and more or less sunken into the tenth segment. The author considers it absolutely necessary to present facts and to leave the final decision to future students, when other specimens shall have been collected. Habitat. Mexico. Type a unique, length 27 mm. ; width 11 mm. Cryptoglossa verrucosa LeConte Cryptoglossa verrucosa LeConte, 1851, Ann. Lyc. Nat. Hist., N. Y., 5; p. 129; Lacordaire, 1859, Genera des Coleopt., 5, 1st. pt., p. 138; Horn, 1870, Revis. Tenebr., Trans. Amer. Philos. Soc., 14: p. 280; Blaisdell, 1943, Proc. Calif. Acad. Sci., (4), 24, p. 223, pi. 11, figs. 10 and 17. A common and moderately large, black, opaque and more or less pruinose species. Pronotum narrower posteriorly than at apex, the latter arcuate and sinuate within the rather large and dis- tinct angles; sides arcuate anteriorly, moderately convergent pos- teriorly before the basal angles, the latter distinct, scarcely promi- nent; base truncate to feebly emarginate. Disk extremely and densely, finely granulate, strongly convex, especially anteriorly; impressions well marked, more or less finely canaliculate on the median line, sublateral strong; base transversely impressed. Scutellum short, triangular and not entering between the elytra. Elytral base applied to the pronotal base; sides arcuate, surface declivous apically, apex subacute. Each elytron has nine series of rather large subarcuate tubercles, the latter obsolete before the apex; surface viewed vertically the tubercles appear irregular and not serial, viewed obliquely and longitudinally from behind they appear in distinct series; more or less variable in size, showing a tendency to become slightly longer than wide at base, toward elytral base they may become smaller, laterally they become rather subacute and the inner or discal appear obliquely elongate to almost subcarinate and most prominent at their apex. The first or sutural interval plane, slightly irregular on surface with scat- tered very small points. Measurements: Length 19-20 mm., width 8-10 mm. Males: Usually smaller and narrower, abdomen moderately convex. Females: Larger, wider and rather more robust, abdomen more convex. Type locality : “In desertis fluminis Colorado.” Distribution : California. San Diego County, May 15, 1911 E. L. Ricksecker) ; Mohave and Colorado Deserts (H. C. Fall) ; Imperial County: La Puerta, August 12; Coachella, May 7, 1917; Salton Sea, April 19, 1916; Indio, March 29, 1924 (L. S. Slevin) ; JANUARY, 1045] BLAISDELL— CRYPTOGLOSSA 25 Los Angeles County (Albert Koebele) ; San Bernardino County: Needles, March 16, 1922 (J. A. Kusche) ; Barstow, April 13 (J. R. Slevin) ; Riverside County: Blythe, Nov. 10, 1924 (F. C. Hadden) ; Palm Springs, May 28, 1916 (J. 0. Martin) ; Kern County: Kings River Canyon (F. Daggett). Arizona. Yuma County: Papago Wells, April 16, 1912; Mohave County: King- man; Pima County: Tucson, Nov., 1921; Santa Catalina Mts., Feb. 5, 1935; N. E. Pima County; S. Pinal County: Picacho, Nov. 10, 1938; S. Arizona. Ajo Mts., Oct. 16, 1935 (Owen Bry- ant). Nevada. Charleston Mts. near Las Vegas, May 24, 1935. Three living specimens were received by the author, April 21, 1933, from a collector in Arizona, two females and a smaller male. The author decided to keep them under observation and on a very restricted diet, rolled oats without water. A glass jar was prepared, by partly filling with sand, covered by a layer of oats. The smaller female died about the sixth year, without any special record. The male died July, 1939, after having lived in the jar for six and one-half years. For diversion and exercise the specimens spent part of their time, clawing and digging into the oats and sand, evidently trying to develop a burrow. The larger female began to show signs of senility at about the sixth year of its confinement; this was noticeable in its dimin- ished activity, with loss of tarsal segments and the two or three terminal segments of the antennae. For the last weeks it scarcely showed signs of life, and died July 10, 1940. During the last weeks a drop of water was placed before it on the table. It would approach the water and sip it up entirely, without any bad effects. The two specimens are preserved in the collection of the Entomological Laboratory of the California Academy of Sciences. Cryptoglossa verrucosa carinulatus Blaisdell, new subspecies Form as in verrucosa LeConte. Frons convex, very sparsely punctate, punctures small in central area, becoming larger and denser apically and laterally. Sides of head broadly and rather feebly emarginate across the position of the oblique sutures, the latter feebly evident or obsolete; epistoma truncate at apex. Men- tum broadly emarginate at apex and somewhat widely margined, surface moderately convex, not sharply nor densely punctate, im- punctate at base; gula transversely rugose. Pronotal disk very densely and finely granulate, a feebly and 26 THE PAN-PACIFIC ENTOMOLOGIST [ VOL. XXI, NO. 1 slightly impressed median line is present, other impressions quite feeble, except a distinct basal sulcus which does not attain the sides. Prothoracic sides slightly irregular, impunctate or very feebly subpunctate, especially anteriorly. Prosternal process broadly margined at apex, surface impunctate or irregularly punctate with intervals rather wide. Elytral intervals in the central area carinulate, each carinula not strong, each divided into carinules by fine transverse fissures, each represents a modified tubercle, which can be seen in speci- mens of verrucosa as subcarinal tubercles; these at the begin- ning of the lateral declivity gradually develop into verrucae, which at first are oblique and angulate posteriorly to form the usual obtuse prominences; sutural intervals plane, finely and sparsely granulate; striae of punctures not distinct; tubercles not sharply defined and broader at base, irregularly involving the intervals. Sternal and parasternal punctures large, well separated and not sharply defined. Abdominal punctures moderate in size; and sparseness, larger and denser laterally especially on first segment; fifth segment with denser and smaller punctures. Male. Usually smaller and narrower, elytra less arcuate at the sides. Female : Broader and subovate, ielytra more arcuate at the sides. Holotype male (No. 5408), and allotype (No. 5409), Mus. Calif. Acad. Sci. Ent., collected by J. R. Slevin, two miles west of Stovepipe Wells, Death Valley, Inyo County, California, May 15, 1931. Paratypes, sixteen, from Furnace Creek, Death Valley, California, collected April 3, 1939, by K. S. Hagen. Albert Koebele secured specimens in Death Valley, April, 1891. J. R. Slevin obtained the species in Panamint Valley, April 29, and also at Balarat, Inyo County, May 13, 1931. Cryptoglossa laevis LeConte Asbolus laevis LeConte, Annals Lyc., N. Y., V, 1851, p. 130. Cryptoglossa laevis LeConte, Revis. Tenebr., Amer. Philos. Soc., XIV, 1870, p. 280. Form similar to that of verrucosa Lee., smaller. Black, some- what shining. Pronotum moderately convex, obscurely punctulate, discal impressions obsolete; base transversely impressed, without marginal bead; lateral marginal bead very fine. Elytra about twice as long as the pronotum, base transverse and slightly wider than the pronotal base; arcuately and rather abruptly declivous at apex; surface obscurely and finely punctulate laterally. Horn states that laevis is smooth and shining, elytra entirely so. Eight specimens studied. Measurements: length 15-20 mm., width 8-10 mm. JANUARY, 104.5] RLAISDELL — CRYPTOGLOSS A 27 Type in the LeConte collection, “long. 65.” Distribution : California: Gray’s Well, Colorado Desert, Im- perial County, Dec. 3, 1927; Westmoreland, Imperial County, May 6, 1933 (E. C. Van Dyke). Arizona: Yuma, May, 1905 (Brown Coll.) ; May 12, 1912 (J. R. Slevin) . Cryptoglossa laevis subsimilis Casey Casey, Memoirs on the Coleoptera, XI, 1924, p. 308. Similar to laevis in form and in the absence of sculpture, but considerably larger and rather more elongate. Color deep black, surface shining, smooth and glabrous. Antennae and legs are somewhat longer than in laevis. In subsimilis the elytra are less smooth, having more numerous feeble striiform lines and stronger punctures toward the sides. Measurements: length 16.5-18.5 mm., width 8. 5-9.0 mm. Type in the Casey collection. Distribution : California: Gray’s Well, Imperial County, July 31, 1940; June, 1911 (E. C. Van Dyke) ; Westmoreland, Imperial County, May, 1933. Arizona: Yuma, March 12, 1912 (J. R. Slevin) ; May, 1910. Number of specimens studied, 8; Col. Casey had two speci- mens when he studied the species. There is some confusion as to which form Casey’s description applies. The author considers it best to give Col. Casey the benefit of the doubt as it is merely a subspecies. Cryptoglossa granulifera Champion Cryptoglossa granulifera Champion, Biol. Centr.-Amer., Col., IV, 1, 1892; Blaisdell, Proc. Calif. Acad. Sci., Vol. XII, No. 12, July 10, 1923, pp. 252-253; Proc. Calif. Acad. Sci. (4) Vol. XXIV, No. 7, February 4, 1943, pp. 223-224. Color black, more, or less dull to slightly shining. Head widest before the eyes, sides more or less arcuately con- vergent anteriorly; epistomal sutures obliterated, apex feebly arcuate in middle two-thirds, thence obtusely continuous with the sides; frontal surface slightly convex, punctures more abundant apically, more or less impunctate centrally and toward base. An- tennae compressed distally, eleventh segment short and truncate. Mentum rounded in form, closely punctate apically, more or less impunctate before the base; apex feebly emarginate and slightly impressed. PTonotum slightly wider at base than at apex, about one-third 28 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 wider than long; disk moderately and rather evenly convex, feebly transversely impressed at base, surface finely and rather evenly punctulate; sides broadly arcuate anteriorly, becoming slightly sinuate in basal third; apical angles prominent and subacute, the basal rather prominent posteriorly but not laterally and slightly less than rectangular. Elytra somewhat oval, about a third longer than wide; base equal to width of pronotal base, more or less abruptly and arcu- ately declivous in apical third; surface with series of moderately small and unimpressed punctures, which become obsolete on the smooth apical declivity, each interval with a series of distantly placed granular elevations, becoming slightly coarser toward the sides, absent apically. Under surface of body opaque and almost impunctate. Pro- sternum broadly and horizontally produced between the procoxae, broadly rounded at apex. Mesosternum sharply raised on either side, and excavated at middle for reception of the apex of the intercoxal process. Measurements: length 18-20 mm., width 8-10 mm. Type locality : Villa Lerdo in Durango, Mexico (Doge.). Five specimens studied. Allied to C. mexicana Champion and C. laevis LeConte, differing from both in having a row of dis- tantly placed granular elevations on each of the elytral intervals, the sutural interval smooth and plane. The elytral sculpture is variable, but the granular elevations are always distinct, becom- ing a little coarser toward the sides. Distribution: Gulf of California: Mejia Island, April 30, 1921; Isle Partida, May 3, and June 26, 1921 (Virgil Owen Coll.). Mexico: Sierra de los Burros, Coahuila, June 18, 1938 (Rollin H. Baker). California: Borrego Canyon, San Diego County, March 22, 1930. Texas: El Paso, June, 1884, and San Antonio. Cryptoglossa angularis Horn Centrioptera angularis Horn, Proc. Calif. Acad. Sci. (2), Vol. IV, 1894, pp. 414-415, pi. VII, Fig. 4; Blaisdell, Proc. Calif. Acad. Sci. (4) , Vol. XXIV, No. 7, February 4, 1943, pp. 223. From all of the known species angularis differs in having the hind angles of the pronotum distinctly everted and the lateral margin in front of them slightly reflexed. Head similar to that of granulifera Champion, but with the frontal margin more evenly arcuate from side to side. Pronotum trapezoidal, broader than long; apical angles acutely prominent anteriorly; sides arcuate, sinuate behind the middle; basal angles acute and moderately everted; disk moderately convex, slightly January, 104.5] BLAISDELL— CRYPTOGLOSSA 20 impressed along 1 the base, surface very finely and sparsely punc- tate. Prothorax beneath slightly rugose. Elytra oval, disk slightly convex to plane, becoming arcuately to somewhat abruptly declivous laterally, obliquely so apically; surface subsulcate, with small distinct murications along the striae, intervals more or less convex, more evidently and coarsely muri- cate laterally, apical declivity smooth before the apex. Abdomen very sparsely punctate. Metasternum with few coarse punctures. Legs densely and coarsely punctate. Measurements: length 20-38 mm., width 10-11.5 mm. Type (No. 109), Museum of the California Academy of Scien- ces; collected at El Paraiso, Lower California. Distribution: Lower California: Las Paz, July 3, 1919, and Santiago, July 22, 1919 (J. R. Slevin) ; Catavina, June 19, 1938 (Michelbacher and Ross). The head is missing in the type. Three specimens at hand show that the eleventh antennal segment is short and transverse, and therefore not a member of the genus Centrioptera Mann. Cryptoglossa mexicana Champion Cryptoglossa mexicana* Champion, 1884, Biol. Centr.-Amer., Vol. IV, Pt. 1, p. 73, Tab. Ill, fig. 21. Opaque, black. Head with a few fine scattered punctures along the anterior margin; men turn coarsely and rather closely punc- tate. Pronotum moderately convex, widened toward the front; apical angles very prominent and triangular; basal angles a little pro- duced, impunctate. Elytra a little broader than the pronotum at base moderately convex, with rows of shallow rounded impres- sions which become obsolete behind the middle, a few scattered raised points at base. Measurements: length 17-19 mm. Habitat. Monclova in Coahuila, Mexico. Champion stated that he had six specimens when he de- scribed the species and according to him it is near laevis Le- Conte: opaque, broader and less convex; thorax broader, wider in front, flatter and less convex, apical angles more produced. Elytra less convex, broader at the base and less rounded at the sides, and with rows of shallow punctures toward base. 30 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 NOTES ON REDWOOD CERAMBYCIDS (COLEOPTERA) BY J. W. TILDEN Santa Cruz, California In the winter of 1932-33 I reared a few specimens of ceram- bycids from Coast Redwood at Santa Cruz, California. Dr. E. C. Van Dyke kindly determined them as his species, Semanotus ligneus sequoiae Van Dyke and Callidium pallidum Van Dyke. There was also one specimen of Opsimus quadrilineatus Mann., a species normally associated with Pseudotsuga taxi folia (Lamb.) Dr. Van Dyke urged me to secure more of these insects, and suggested further rearing. Redwood second growth that had been attacked in the forest by Cerambycidae was stored in wooden boxes indoors in the winter of 1933-34, but with poor results, as only a few specimens were obtained. It was found that mortality at emergence was very high. This may have been due to greater dryness since these in- sects are normally exposed to very damp weather. In March, 1935, a second growth redwood about ten inches in diameter was cut down in the woods. It remained exposed to attack all summer, and in the fall was found to be heavily in- fested with beetle larvae. In March, 1936, an examination of the tree showed that the beetles had transformed from pupae to adults and were ready to emerge. To prevent normal emergence and loss, they were re- moved from the tree, so that the normal date of emergence was not obtained. Collection dates of free specimens taken in the same locality range from late February to the middle of April in these same species. The number of adults removed from this one tree was large: upwards of 70 specimens of Semanotus ligneus sequoiae, about 150 of Callidium pallidum, and in the upper small branches, a number of specimens of Phymatodes nitidus Lee. In addition to these, a few specimens of Callidium sempervirens Linsley were taken from the twigs at the tip of the tree. Larvae of T emnocihila virescens (Fab.) and a single raphidid larva were found in the burrows of Semanotus, while an unidenti- fied fungus killed some pupae; but on the whole these beetles seemed remarkably free from both parasites and predators. JANUARY, 19451 CAMRAS— ZODION 31 From the available data, the following conclusions are drawn: 1) These cerambycids attack the Coast Redwood and develop in freshly cut or injured wood (especially in second-growth timber or in limbs?). The larvae first feed in the drying cambium and later in the sapwood, but eventually may bore deeply into the wood. They usually return nearly to the surface, just below the bark, to pupate. The species observed develop from egg to adult in one year. 2) They show specific preference for certain parts of the tree. Semanotus is found in the main trunk of second-growth trees, Callidium pallidum Van Dyke occurs in the branch- bearing part of the trunk and in the larger branches, while sempervirens and Phymatodes nitidus prefer the smaller branches and trees. 3) These species are less rare than previously supposed, and proved able to build up large populations under optimum conditions such as those afforded by the presence of a freshly cut tree at the time of oviposition. 4) Opsimus quadrilineatus Mann., previously associated only with Pseudotsuga taxi folia (Lamb.) seems able to utilize Sequoia sempervirens (Lamb.) as a food supply. FURTHER NOTES ON SOME SPECIES OF ZODION (Diptera, Conopidae) Since the publication of notes on the Zodion fulvifrons group, the author has visited the museums in the East and has examined many types. As a result, the following changes must be made: Zodion reclusum Banks. The type has some reddish on the sides of the second abdominal segment not mentioned in the original description. There is also much yellowish on the other segments and therefore belongs under fulvifrons rather than as a synonym of intermedium. Sicus brevirostris Coquillett (1902, Canad. Ent. 34:198 — Mexico: Chihuahua: Sierra Madre). This species is a Zodion, the second segment of the proboscis noted by the describer be- ing the labellae. The palpi are clubbed, two to two and one- half times the width of the proboscis; and the species does not seem to differ from palpale. Zodion bimacula Curran. The type is an individual in which the distal portion of the proboscis is broken off. It is a speci- men of Occemyia loraria Loew. — Sidney Camras. 32 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 NOTES ON SOME MOTHS OF THE FAMILY SATURNIIDAE (Lepidoptera) BY J. W. TILDEN Santa Cruz, California While collecting in the Pozo Mountains in the general region of La Panza, San Luis Obispo County, on March 23, 1940, George Mansfield and the author took three male specimens of a Calo- saturnia sp. This area is a typical chaparral association of Ceanothus, Arc- tostaphylos, Cercocarpus, Adenostoma, Photinia, Dendromecon, with Quercus spp. in the canyons. The specimens were taken flying in typical undulating fashion over the chaparral on the west side of the divide. I have been informed by Mr. J. W. Johnson (personal com- munication) that there exist to his knowledge no previous records of this genus from San Luis Obispo County. Inasmuch as this area is outside of the habitats of his two recently described spe- cies of Calosaturnia, C. albofasciatus Johnson and C. meridion- alis Johnson, it appears probable that the specimens from the Pozo Mountains are referable to Calosaturnia mendocino (Beh- rens), the type species of the genus, thus extending the already wide known range of the species. In July, 1941, six larvae of C. mendocino were taken in the Santa Cruz Mountains. All were of the pink or orange color phase, none being of the dark or green phase. Of these, three pupated in typical satumiid cocoons in a few days. Two others succumbed to A panteles parasites, and a sixth disintegrated, pos- sibly from a bacterial disease. Of the three pupae, one emerged in an injured condition on January 17, 1942. About the same time, a second pupa produced a tachinid. The third pupa did not develop either adult or parasite. The food plant of the larvae taken was Arbutus menziesii Pursh. Several of our party com- plained of the stinging setae of these larvae, and I personally discovered that the setae are indeed quite painful, however, the effect does not last long. In late July, 1941, a few days after the mendocino larvae were taken, over 50 larvae of P seudohazis eglanterina were obtained from Ceanothus thyrsiflorus Esch. These larvae were almost ma- JANUARY, 1045] NOMENCLATURE COMMITTEE 22 ture when taken, and after feeding for from one to eight days, either succumbed to parasites or attempted to pupate. Thirty- one died from Apanteles parasites. Others formed cells even when covered with Apanteles cocoons, but failed to pupate. Only six pupae formed from the total number, and of these six, five emerged tachinids during the winter. Only a single adult was obtained from more than fifty larvae. I do not believe this to be an extreme case of parasitism. An almost similar result was ob- tained from larvae of Papilio philenor hirsuta Skin., in 1938, from Putah Canyon, Yolo County, California. Where larvae are taken nearly full grown, parasitism is far more marked than in larvae taken in the early instars. While collecting in the White Mountains of California, near Benton Station, Mono County, C. W. Bowles and the author took a large number of satumiid larvae on Salix sp., along a small watercourse. In view of the location and the food plant, these are circumstantially considered to be the larvae of Platysamia gloveri Stkr. Attempts to rear these larvae resulted in complete failure, all specimens falling victims to Apanteles previous to pupation. I have been informed by Mr. J. W. Johnson that this is the first record of larvae of this species from a California locality, although the adults have been taken within the state on several occasions. Mr. Johnson agreed that the larvae were most likely to be gloveri, and suggested the inclusion of their occurrence, in these notes. It seems logical that gloveri should include in its range that part of California which falls within the Great Basin region. AMERICAN COMMITTEE ON ENTOMOLOGICAL NOMENCLATURE The name of the American Commission on Scientific Nomen- clature in Entomology has recently been changed to American Committee on Entomological Nomenclature. The present officers are C. F. W. Muesebeck, Bureau of Entomology and Plant Quar- antine, Washington 25, D. C., Chairman, and E. G. Linsley, Uni- versity of California, Berkeley 4, California, Secretary. Commu- nications may be addressed to either of the above officers. 34 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 PACIFIC COAST ENTOMOLOGICAL SOCIETY M. A. Stewart, President F. P. Keen, Vice-President E. G. Linsley, Secretary R. C. Miller, Treasurer Proceedings One Hundred and Eighty-first Meeting The one hundred and eighty-first meeting of the Pacific Coast Entomological Society was held at 2:30 p.m. on March 25, 1944, in the entomological laboratories of the California Academy of Sci- ences, San Francisco. President Stewart in the chair. The follow- ing members were present: M. A. Stewart, E. G. Linsley, F. M. Prince, E. C. Van Dyke, D. N. Murphy, A. E. Michelbacher, C. D. Duncan, W. C. Reeves, P. Moorhead, F. N. Driver, R. F. Smith, R. W. L. Potts, J. L. Gressitt, E. R. Leach, R. C. Miller. Visitors were present as follows: Mr. Pedro Galindo, Mr. M. W. Allen, Mr. M. Reed, Miss B. Patterson, Miss B. J. Franseen, Mr. G. L. Brown, Mr. T. Hutchins, Mr. A. Branngan, Mr. J. E. Ryus, Mr. W. J. Chamberlain, Mr. M. Marquis, Mr. M. Garcia, Mr. J. McCarty, and Mr. R. Schuster. The minutes of the previous meeting were read and approved. The Membership Committee proposed the following names for membership : Mr. Paul R. Jones, Mr. A. L. Deaver, Mr. Pedro Galindo, and Mr. M. W. Allen. The motion was made and passed that the Secretary cast a unanimous ballot for their election. President Stewart raised the question of the desirability of holding an annual field trip in 1944. After some discussion, Mr. R. F. Smith moved that in view of transportation difficulties no attempt be made to hold a field trip this year. The motion was seconded and passed. Dr. Van Dyke moved that a meeting be held at the Academy in the latter part of June in place of the annual field trip. The motion was seconded and passed. Dr. Duncan, Dr. Van Dyke, and others reported the where- abouts and present assignments of various Society members now serving in the armed forces. Mr. R. F. Smith reported that he was anxious to learn the effect of the current abnormally dry season upon the populations of Colias eurytheme. He requested members to be on the look-out for information on the subject whenever the opportunity arose. Dr. Duncan recorded finding unusually long Gordian hair worms in Jerusalem crickets in San Jose, one thirteen inches long, an- other twenty-eight inches long. He mentioned that the worms had emerged in a dry environment in the absence of water. Mr. Allen JANUARY, 104.5] PACIFIC COAST ENT. SOCIETY 35 commented that specimens 36 and 42 inches long" had been re- corded from the Mormon cricket. President Stewart then presented Mr. J. Linsley Gressitt, a Society member recently repatriated from occupied China, who addressed the Society upon “Entomological Experiences in China.” Mr. Gressitt stated that the experiences of an entomologist sta- tioned in China are apt to be very different from those of one in this country. For entomology is practically undeveloped in China, as compared with the United States. Entomology has been largely fostered in China by Americans and French, particularly as far as education in entomology within China is concerned. The Japanese have also played a part. Much of the early insect collecting in China was done by French, British, Russians and Germans. Edu- cational institutions playing the main role in China in recent years include the American Christian Colleges in China, among them Lingnan University of Canton where the speaker was stationed for four years or so, the French Catholic universities in Teint- sin and Shanghai, and several of the Chinese national universities, such as Sun Yat-sen, Kwangsi, Szechuan, Central, and others. Research institutions in China dealing with entomology include the Academia Sinica and the National Agriculture Research Insti- tute, both to some extent subsidized by American money, and the Shanghai Science Institute, a Japanese institution. Other organ- izations such as the Science Society of China have fostered re- search and publication. Among entomologists prominent in China Mr. Gressitt men- tioned Sicien Chen and his wife Yon-yon Zia of the Academia Sinica, C. F. Wu of Yenching University, F. C. Wu and Gaines Liu of the National Agriculture Research Institute, C. L. Liu of Tsing-hua University, C. Y. Liu of Kwangsi University, Prof. W. E. Hoffmann of Lingnan University, Prof. C. R. Kellogg of Fukien Christian University, Prof. B. A. Slocum of the University of Nanking, Prof. A. W. March of Hangchow Christian College and Fathers 0. Piel and B. Becquart of Universite l’Aurore in Shanghai. Several American entomologists have in the past spent one or more years teaching or helping to organize entomology in China. These include J. G. Needham, C. W. Woodworth, E. C. Van Dyke, W. A. Riley and C. W 1 . Howard. The latter two were at Lingnan University, where also Dr. R. C. Miller, director of the California Academy of Sciences, was in charge of zoology for a time. Prominent works on Chinese insects or entomology referred to by Mr. Gressitt included G. F. Wu’s “Catalog of Chinese Insects” and works on aquatic insects, Needham’s “Dragonflies of China,” Hoffmann’s “Catalog of Scutelleroidea . . . ,” Ouchi’s “Bibliography of Chinese Insects,” Yang’s work on Heteroptera, work on Orthop- tera by Chang and Tinkham, on Homoptera by Metcalf, Funk- hauser and Gaines Liu, on Siphonaptera by C. Y. Liu, Vespidae by C. L. Liu and Coleoptera by Sicien Chen and the speaker. Some 36 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 groups, such as Diptera, Hymonoptera, Lepidoptera and others, have hardly been studied except for scattered descriptions of species published in Europe. Economic entomology is even less developed than systematic entomology in China. This is partly for economic reasons since the low living standards of Chinese farmers prevents their utiliz- ing chemical control of insect pests on their own account, and also may be partly due to the difficulty of changing long-estab- lished agricultural practices. The lag is also in part attributable to lack of government funds for agricultural research and a scarcity of well-trained entomologists. With the help of the insti- tutions mentioned above, and the impetus of the war, rapid prog- ress is being made in certain lines, in spite of the difficult condi- tions that prevail at present. At present about the only general types of control that can be recommended are cultural and mechanical methods, since chemicals are practically unavailable, even if the farmers had the means to buy them. Before agricultural entomology can be brought to com- pare in any degree with that in the United States, the living standards of the farmers, who form a large part of the population of China, must be improved or the government must furnish mate- rials and machinery for cooperative use. Biological control offers an undeveloped field in China, but may not play as great a part as it does in this country since many of China’s serious pests are native, and a lesser proportion introduced from foreign countries than is the case here. Among prominent pests the speaker encountered in South China were the Laichee Stink-bug, rice borers, rice beetles (criocerids and hispids), roundheaded borers, scales, bugs, and leaf -hoppers on Citrus, lantern flies and other fulgorids on various fruit trees or shrubs, mulberry and fig borers (cerambycids) , flea-beetles and galerucids on vegetables, Citrus and other plants, the banana weevil and banana leaf -roller (a large hesperiid), the Laichee and Lung- ngan (Longan) cerambycid borer, wax-moth, cabbage butterfly and grain weevils and moths. Mr. Gressitt reported that his work at Lingnan University largely concerned the care of the collections in the Lingnan Natu- ral History Museum and the development of the insectary of the Natural History Survey where the life-histories of many of the local insect pests were being studied. Complete preserved mate- rial of the immature stages of these pests or local insects was being assembled, as well as data. The speaker also had the oppor- tunity of making three trips into Free China, two in northern Kwantung and the other through Indo-China into Yunnan, Kwei- chow and Szechuan provinces in West China, as well as collecting in Hong Kong from time to time. Because of the Japanese occu- pation of Canton, Lingnan University was divided in several places: Canton, Hong Kong and later Free China. Thus the edu- cational as well as research and travel facilities were consider- JANUARY, 1945] PACIFIC COAST ENT. SOCIETY 37 ably hampered. In addition to work for Lingnan University, the speaker spent a few months collecting parasites of the red scale in Hong Kong and Canton for shipment by clipper to California, for the Citrus Experiment Station of the University of California. After the United States entered the war Prof. Hoffmann and the speaker were allowed to continue research on the Lingnan campus for about a year and were even able to publish several papers, called Special Publications of the Lingnan Natural History Survey and Museum. Following this period came internment and then repatriation to this country via the “Gripsholm” in December, 1943. Mr. Gressitt’s talk was accompanied by movies and slides taken at Canton, Hong Kong and in Free China. Following a discussion of Mr. Gressitt’s paper the meeting ad- journed. — E. G. Linsley, Secretary. One Hundred and Eighty-second Meeting The one hundred and eighty-second meeting of the Pacific Coast Entomological Society was held at 2 p.m. on June 24, 1944, in the entomological laboratories of the California Academy of Sciences, San Francisco. President Stewart in the chair. The following members were present: M. A. Stewart, E. G. Linsley, R. C. Miller, J. L. Gressitt, R. F. Smith, E. C. Van Dyke and E. 0. Essig. Visitors were present as follows: Prof. Herman A. Scullen, Mr. Joseph E. Ryus, and Mr. William Russell. The minutes of the previous meeting were read and accepted. The Membership Committee proposed the following names, Dr. Heber C. Donohoe, Mr. D. A. Zanette, and Mr. Charles Parsell, Jr. They were duly elected to membership. Dr. Van Dyke exhibited a new species of dobson fly, Neohermes nigrinus Van Dyke, calling attention to the fact that much work in neuropteroids remains to be done in the west. He also exhibited two boxes of Coleoptera sent by Dr. Ross from New Guinea. He noted especially a species of Pachyrhynchus, a group formerly thought to be restricted to the Philippine fauna. Dr. Van Dyke reported the capture in the spring of 1944 of a mating pair of Bombus vosnesenskii. The female was freshly emerged. The male appeared worn. He stated that it was gener- ally believed that bumblebees mated in the autumn only, but this observation suggested that there were two broods. Dr. Linsley re- marked that in 1942 he had captured large numbers of males of B. edwardsii and a few of B. vosneseskii and B. sitkensis in early spring in Madera and Mariposa counties and in the previous year had taken a few males of edwardsii in Shasta County. He sug- gested that the production of vernal males might be characteristic of certain western bumblebees and expressed the opinion that it did not necessarily imply two broods. President Stewart then presented Dr. R. C. Miller who ad- dressed the Society on the subject “What is a species?” Dr. Miller stated that as soon as the Linnean concept of a species as a sep- 38 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 arate, permanent, and more or less easily recognizable, entity began to prove untenable, the whole problem of what constitutes a species fell into a state of confusion from which it has not emerged. Thus one finds views of working taxonomists ranging all the way from those who believe that positive (e„g. genetic) criteria can be found for segregating species to those who frankly consider species to be arbitrary groupings of individuals for the convenience of biologists in arranging or discussing them. As a matter of fact, even taxonomists who adhere to the former of these ideas in theory, often follow the latter in practise. Accord- ingly, as a working definition Dr. Miller proposed consideration of the following: “A species is a group of closely similar organisms segregated on the basis of characters that can be recognized by the average trained biologist.” Many will object that “specialist” should be substituted for “average trained biologist.” But if we grant this, we drift dan- gerously toward taxonomic authoritarianism, under which a spe- cies becomes whatever Dr. X or Professor Y says is a species. The lack of agreement as to what constitutes a species empha- sizes the importance of the type, and of promptly depositing type material in a recognized museum where it will be permanently available for study by present and future investigators. After a discussion of Dr. Miller’s paper the meeting adjourned. — E. G. Linsley, Secretary. One Hundred and Eighty-third Meeting The one hundred and eighty-third meeting of the Pacific Coast Entomological Society was held at 2:30 p.m. on October 7, 1944, in the entomological laboratories of the California Academy of Sciences. The following members were present: F. P. Keen, E. G. Linsley, R. F. Smith, J. L. Gressitt, N. F. Olson, A. E. Michel- bacher, C. D. Duncan, E. C. Van Dyke, P. Moorhead, and R. W. L. Potts. Visitors were present as follows: E. A. Steinhaus, A. L. Burroughs, P. H. Arnand. The minutes of the previous meeting were read and approved. The Membership Committee proposed Prof. H. A. Scullen for membership in the Society. He was duly elected. Dr. E. C. Van Dyke exhibited six boxes of mounted insects from the more than fifty thousand specimens sent back by Dr. E. S. Ross from New Guinea. Dr. C. D. Duncan exhibited an extremely interesting collection of unusually grotesque neotropical Membracidae. Pie also called attention to the discovery at Mt. Hermon in Santa Cruz County, California, of a large colony of Vermelio, a genus which had been previously regarded as restricted to higher elevations in the state. Mr. R. F. Smith reported a large migration of Aglais calif or- nica late in the summer of 1944 and called attention to the fact that he was preparing a summary of the literature pertaining to January, 104 . 5 ] PACIFIC COAST ENT. SOCIETY 30 migrations of this species and would welcome any first-hand ob- servations on the subject. Mr. F. P. Keen remarked that early in the season there was a serious outbreak of the caterpillar on Ceanothus in the Shasta region. Mr. Keen also commented that in general this had been a year of minor barkbeetle activity along the Pacific Coast but that de- foliators had been serious in certain local areas. He mentioned particularly outbreaks of Perionia variana, and a lodgepole pine sawfly {Neodiprion sp.). The latter species was responsible for the defoliation of about 25 square miles of lodgepole pine in Ore- gon, as a result of an infestation which had apparently been building up for at least three years. In response to a question by Dr. Linsley, Mr. Keen commented on an outbreak of the Englemann spruce beetle in the Grand Mesa and White Mesa, Colorado. The species had not previously been observed in epidemic numbers for a great many years. Mr. Keen then presented Prof. Edward A. Steinhaus of the Department of Bacteriology, University of California, who deliv- ered an illustrated lecture on Intracellular Organisms in Insects. Prof. Steinhaus pointed out that some of the most interesting of all biologic relationships between microorganisms and insects are those of intracellular parasites and symbiosis. Within the tissue cells of many arthropods may be found apparently living, non- pathogenic organisms. These intracellular organisms frequently live in specialized cells or structure called mycetocytes and myce- tomes. Various types of these were discussed and illustrated by lantern slides. These organisms are not only transmitted directly from one generation to the next but they are also present in every representative of the species. In the case of the aphids the path of transmission of the symbiotes was traced from the follicular epithelium of the parent to the definitely formed mycetome of the offspring. In certain bostrychid beetles, the organisms from the mycetomes invade the lobes of the testes, multiply, and mix with the sperm. They then pass through the micropyle of the fully formed egg during its passage to the outside, and thus the infec- tion is accomplished. Transmission of the symbiotes via the out- side of the egg shell was shown in the case of Stegobium paniceum. Other intimate and little understood relationships were discussed and illustrated. For the most part these intracellular organisms are of the nature of bacteria or yeasts, and occasionally fungi. As to the role of these symbiotic microorganisms in the life processes of the host very little definite information is at hand. In some cases, at least, the symbiotes apparently supply vitamins necessary for normal insect development. After a discussion of Dr. Steinhaus’ paper, the meeting was adjourned. — E. G. Linsley, Secretary. One Hundred and Eighty-fourth Meeting The one hundred and eighty-fourth meeting of the Pacific Coast 40 THE PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 1 Entomological Society was held at 2:30 p.m. on January 6, 1945, in the entomological laboratories of the California Academy of Sciences. The following members were present: M. A. Stewart, E. G. Linsley, F. P. Keen, E. C. Van Dyke, P. Moorhead, A. E. Michelbacher, W. M. Pearce, R. W. L. Potts, R. F. Smith, M. W. Allen, J. L. Gressitt, R. C. Miller, and C. D. Duncan. Visitors were present as follows: Mr. L. R. Brown, Mr. R. P. Allen, Mr. J. Gomez. Dr. E. A. Steinhaus, Miss R. Noakes, Mr. A. L. Burroughs, Mrs. B. Prendergast, and Miss H. L. Pehrson. The minutes of the previous meeting were read and approved. The Membership Committee proposed Prof. Carl J. Drake, Dr. E. A. Steinhaus, Mr. Robert P. Allen, and William Peterman, Inc., for membership in the Society. They were duly elected. President Stewart asked for the annual report from the Treas- urer. Dr. Miller presented the report and Dr. Van Dyke moved that the report be accepted and that the Society extend its thanks to Dr. Miller for the excellent work wihch he had performed in connection with this office. The motion was seconded and unani- mously passed. The Nominating Committee proposed the following officers for 1945: F. P. Keen, President; C. D. Duncan, Vice-president; E. G. Linsley, Secretary, and R. C. Miller, Treasurer. The motion was made, seconded and passed that the Secretary cast a unanimous ballot for their election. Dr. Stewart turned the chair over to the new president, Mr. Keen, after expressing appreciation to the officers and members for support which had been extended to him during his term of office and after calling attention to the great responsibility which scientific societies must assume at present in order to maintain standards and culture in the face of strong pressures to the con- trary. Dr. Van Dyke exhibited a copy of G. V. Hudson’s “The Butter- flies and Moths of New Zealand” which the Academy had recently received as a gift from the New Zealand legation in Washington. Dr. Steinhaus mentioned his interest in bacterial, protozoal and viral diseases of insects and expressed the hope that members would assist him in the collection of material for study. Mr. Keen then presented Dr. Stewart who delivered a most thought-provoking address entitled “Professional Training in En- tomology” (seep. 1). Following Dr. Stewart’s address, the meeting adjourned. — E. G. Linsley, Secretary. REVISTA DE ENTOMOLOGIA An International Review of Entomology An illustrated magazine published four times a year by THOMAZ BORGMEIER, O.F.M.. devoted to entomology, mainly of the neo- tropical fauna. The volumes already published since 1931 comprise thousands of pages and contain articles by leading entomologists such as F. W. Edwards, W. Horn, E. Lindner, J. W. S. Macfie, E. Martini, A. da Costa Lima, F. Silvestri, C. Menozzi, A. Reichensperger, F. Santschi, J. D. Hood, etc., with a bibliography of the current literature (economic and non-economic) of the neotropical fauna. Annual subscription $4.00 U. S. ($5.00 U. S. through booksellers). All payments are in advance. The back volumes are still on sale; price of each volume 4 U. S. dollars; through booksellers 5 U. S. dollars. Subscriptions should be sent to the Editor: Thomaz Borgmeier, O.F.M., Convento 3. Antonio, Largo da Carioca, Rio de Janeiro, Brazil. ARCTIC LEPIDOPTERA A large collection of Arctic Lepidoptera, especially Erebia, Oeneis, and Noctuidae, has been accumulated. Collectors who desire such material please communicate with me as follows: R J. Fitch, Lloydminster. Saskatchewan, Canaaa. ENTOMOLOGICAL NEWS An illustrated magazine, published monthly — except August and September — devoted to the study of INSECT LIFE. It contains a list of the titles of the current Literature on American Entomology, articles by the leading authorities in the United States and Canada. It is a nee* essary journal of reference for working entomologists, and contains valu- able information for economic and systematic students. Annual subscription price $3.00. Foreign (except Canadian $3.15) subscriptions S3. 30. Single copies 35 cents. Address ENTOMOLOGICAL NEWS, 1Q00 Race Street, Philadelphia, Pa. Vol. XXI April, 1945 No. 2 THE Pan -Pacific Entomologist Published by the Pacific Coast Entomological Society in co-operation with The California Academy of Sciences CONTENTS GOLDSCHMIDT, EVOLUTION OF MOUTH PARTS IN DIPTERA— A COUNTER CRITIQUE 41 HARE, FLYING STAGE OF THE DEER LOUSEFLY, LIPOPTENA DEPRESSA (SAY), IN CALIFORNIA 48 SAMPSON, FIVE NEW SPECIES OF ALEYRODIDAE FROM CALIFORNIA 68 SEEVERS, NEW GENERA AND SPECIES OF TRICHOPSENIINAE FROM AMERICAN AND AUSTRALIAN TERMITE NESTS 63 FENDER, OREGON CHRYSOMELIDAE 72 JENSEN, NOTES ON THE SYNONYMY, NYMPHS AND DISTRIBUTION OF HETEROPSYLLA TEXANA CRAWFORD 74 FENDER, NOTES ON THE SPECIES OF PODABRUS OF OREGON AND WASHINGTON 77 San Francisco, California 1945 THE PAN-PACIFIC ENTOMOLOGIST EDITORIAL BOARD E. C. Van Dyke E. G. Linsley R. W. L. Potts Associate Editor Editor Assistant Editor R. L. Usinger* G. F. Ferris E. S. Ross* R. C. Miller, Treasurer • On military leave Published quarterly in January, April, July, and October with Society Proceedings appearing in the January number. Papers on the systematic and biological phases of entomology are favored, including articles up to ten printed pages on insect taxonomy, morphology, life history, and distribution. Manuscripts for publication, proof, and all editorial matters should be addressed to the editor, E. G. Linsley, 112 Agriculture Hall, Uni- versity of California, Berkeley, California. All communications regard- ing non-receipt of numbers, changes of address, requests for sample copies, and all financial communications should be addressed to the treasurer, R. C. Miller, at the California Academy of Sciences, San Francisco, California. At least twenty-five “author’s extras” will be supplied free of charge. Additional copies will be reprinted at cost of publication, if a request is received when proof is returned. Domestic and foreign subscriptions $2.50 per year in advance. Price for single copies 75 cents. Make checks payable to “Pan -Pacific Ento- mologist.” INSECT BOXES Standard size black insect box with sides of box and cover made of l/t" redwood. The top, bottom and shoulders are of heavy cardboard. Inside dimensions: I2%x8%x2% inches. Prices: 60 cents each. Lots of one dozen, 50 cent* each. With Masonite bottom, 15 cents extra. With glass top, 50 cents extra. Prices for larger quantities on request. Unit boxes also manufactured Prices on application RAISIN AND THIEBAUT BROS., LTD. 346 First Street, San Francisco, Calif. Entered as second class matter, February 10, 1925, at the postoffice at San Francisco, California, under Act of August 24, 1912. Tli e Pan-Pacific Entomologist Vol. XXI, No. 2 April, 1945 EVOLUTION OF MOUTH PARTS IN DIPTERA A COUNTER CRITIQUE BY RICHARD B. GOLDSCHMIDT University of California, Berkeley In a recent review of that homoeotic mutants of Drosophila my former student, C. Villee, made some statements on homologies of Dipteran mouth parts (taken over from Bridges and Dobzhan- sky’s paper on the Drosophila mutant proboscidea ) . Later he commented briefly, though rather dogmatically, on the evolu- tionary significance of those mutants, following the present au- thor’s viewpoints as developed in a recent book (1940). Villee’s remarks on both these topics have been strongly criticised by the excellent entomologist, G. F. Ferris. As this criticism does not involve questions of entomological detail unknown to the out- sider, but broad and general problems of evolution it ought to be considered carefully and discussed by non-entomologists. Ferris’ first, rather acid critique was directed against the geneticist’s claim to have established some decisive arguments in controversial problems of homology. The organ under discussion is the oral lobe or labellum in the proboscis of Diptera. Old authors (Lowne) homologized it to the maxillae, but this had been given up long' ago by dipterologists, some of whom consid- ered the oral lobes as derived from the paraglossae while the more modern view derives them from the labial palpi. Villee, repeating remarks made by Bridges and Dobzhansky, pointed out that the mutant proboscipedia with antennae or tarsi instead of the oral lobes proves definitely that Lowne was wrong. He did not further discuss the development of the problem subsequent to Lowne’s paper because part of the literature had been quoted by Bridges-Dobzhansky whom he followed in his discussion. Ferris rebuked rather strongly the geneticist who assumes the right to decide upon a problem of comparative morphology. He wrote: “So far, so good. This is merely a fact which is well enough known to any morphologist of the present day and the contribution of genetics is not necessary to confirm it.” Further, after quoting Villee’s remark that the mutant shows that the oral 42 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 lobes are homologous to labial palpi, he said: “Villee seems to have been unaware of any work that has been done in the mor- phology of insects since the date of Lowne (1890), for evidence has been presented on morphological grounds alone, by at least three authors, which demonstrates beyond any reasonable doubt that the ‘oral lobes’ of flies are in fact nothing more than the labial palpi. We should not object to such confirmation of our morphological ideas as we can gain from geneticists . . . . ” This discussion, I think, has a significance beyond the present bone of contention. The present writer, who had passed the in- criminated sentences for publication though overlooking the lack of reference to the modern interpretation, cannot be accused of lack of understanding for the morphologist’s point of view, having spent many years of his life in work on comparative mor- phology and having been guilty of many more or less good phylogenetic homologisations on the basis of such work. But, I think, everybody ought to realize that problems of homology can, in many cases, be settled only by experimental, embryological, or genetical work. By comparing many different types the mor- phologist comes to definite conclusions the correctness of which increases with the quantity of the material available. Sometimes there will be no reasonable doubt for a homologisation and the actual proof furnished by the experimental work might amount to carrying owls into Athens. To take an example: The homo- logisation of the halteres of flies with wings is beyond any rea- sonable doubt. Thus the fact that a haltere may be transformed into a wing ( Drosophila mutant tetraptera ) or a wing into a haltere (mutant telraltera) is not needed to establish the homol- ogy. But there are many homologies for which the situation is different and different schools draw different conclusions. To take again an example: There has been much discussion and di- vergence of opinion regarding the homologies between female and male genital armature and ducts in Lepidoptera. Some points could be settled by the study of development, but other homol- ogies could only be finally established (by Goldschmidt and Kosminsky) when the geneticist produced all grades of inter- sexes in which the transformation of one part into the other (or the impossibility of it) could be seen. The supreme criterion of homology is experimentally transforming one member into the other. APRIL, 1 945 ] GOLDSCHMIDT — MOUTH PARTS IN DIPTERA 43 In spite of Ferris’ claims to the contrary and the condescend- ence apparent in the above quotation, I hold that the situation is not much different in the material under discussion. Though, no doubt, the present trend among dipterologists is to assume that the labella are the homologues of labial palpi, it cannot be over- looked that very good entomologists have held (and might still hold) that the proper homologues are the paraglossae. In the most recent general presentation of the subject known to me, the Dipterologist Hendel writes (1936) : “ A generally accepted homologisation does not yet exist. 1 According to Peterson sub- mentum and mentum are united more or less closely with the membrane of the sixth head sternite. He calls the boatshaped chitinous plate located ventrally in the labial proboscis the theca; he homologises the labella with the paraglossae as do Newport and Gershfield. I follow in the homologisation of the labial parts those authors who interpret the just mentioned ven- tral chitin plate of the trunk as the mentum, and the labella as labial palpi (Burmeister, Becher, Hewitt, Frey) Almost at the same time Snodgrass (1935) writes in his well-known text: “The labella . . . have been generally regarded as the paraglossae, apparent rudiments of the glossae being sometimes present be- tween them; but Crampton . . . has given reasons for believing that the labellar lobes are the labial palpi. Palpi, however, are typically provided with antagonistic muscles. The lobes of the fly labrum have usually only one muscle inserted directly upon it.” Thus the standard entomological text does hardly consider Crampton’s (and others) homologisation established “beyond reasonable doubt” and actually is leaning toward the other side. To these statements I may add that among the old and new authors who agree with Frey are Erickson (1840), Kraepelin (1880), Griinberg (1907), Crampton (1923-25), Jobling (1927). Among those who are opposed to the homology of the labella with labial palpi are Wesche (1904), McGillivray (1924), Otanes (1922). The detailed and animated polemic on the sub- ject between Crampton and McGillivray proves sufficiently that a final decision satisfying everybody cannot be reached by mor- phological comparison alone. (Professor E. G. Linsley has kindly drawn my attention to Crampton’s most recent paper, 1 Translated from the German ; italics mine. 44 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 1942, in which he summarizes the data in favor of his interpreta- tion and gives clearer drawings of mouth parts of Mecoptera and Diptera than contained in former publications.) Thus to me these statements and facts convey the idea that the problem is still controversial and not solved “beyond any rea- sonable doubt” by comparative morphology. The genetical facts reported above furnish a complete proof of the interpretation. The geneticists who claim this (following Bridges and Dobzhan- sky, the latter himself trained as an entomologist) do not want to parade any superiority but just make the proper use of a superior tool, which they happen to wield. There is a second part to Ferris’ criticism. Villee had stated, following certain of the present author’s views (1940) that the homoetic mutants demonstrate that it is not necessary for ex- ample, to assume that the oral lobe has been developed from the biting parts of lower insects by accumulation of small steps. Rather a single mutation affecting early embryonic processes may have effected this in one step. He adds, somewhat overshooting his mark, that animals with intermediate mouth parts would not have been able to feed. 2 To this Ferris remarks: “All of which can but wring an agonized scream from the depths of a mor- phologist’s soul. The writer of that statement, like most non- entomologists, seems to be quite unaware of the fact that there are thousands upon thousands of species of flies other than Drosophila melanogaster and that these flies present probably hundreds of those various ‘intermediate types of mouth parts’ condemned by him, with which they get along very nicely. These degrees of development range from the perfectly normal, although but two-segmented palpus in the closely related and possibly even antecedent order Mecoptera through various modifications up to the highly bulbous palpi of the most specialized flies ...” This statement clearly characterises my viewpoint, as repeated by my student, as based upon ignorance. But it may be assumed that a former, though rather amateurish collector of insects, including Diptera and Mecoptera, is familiar with the existence of flies other than Drosophila. Recollecting the structure of the many mouth parts of Diptera which I had once dissected in entomol- ogical classwork, I was unable to remember having seen all these transitions. Therefore, I asked Ferris by letter to name a few of 2 My own statement (1940) of which this is a paraphrase says that gradations between generalized and specialized types would have died of starvation. APRIL, 1945 ] GOLDSCHMIDT MOUTII rARTS MrTEIfcA 45 the hundreds of transitional stages which he had in mind and to help me to collect information on them. As no answer was re- ceived, I took the trouble to search for these transitions, believing that there might be an alternative to ignorance so complete that it makes souls scream: namely a different evaluation of what might be considered a transitional stage. Again I consulted first the most recent monograph on Diptera by Hendel and found the following statement: “The labella or labial palpi are separate externally in primitive forms, inde- pendent but connected basally by a hyaline middle part which may be swelled. This connection has become more close in the course of evolution, especially in the Calyptrata.” This statement, in my opinion, covers the crux of the matter. In the papers of Peterson, Frey, Crampton and Jobling descriptions can be found of the mouth parts and their comparative interpretation and in some of them detailed, in others only semi-diagrammatic figures. The interest centers upon the forms which are considered primi- tive by dipterologists. Crampton studied what he calls the most primitive living representative of the order Diptera, Tanyderus. Frey (1913) analysed a series of primitive types as Bolitophila, Gnoriste, Sciara, etc. Jobling (1927) discussed Culicoides. In all these cases we have the typical elongated labium whatever the homologisations of the parts with the mentum, submentum and palpiger of lower forms may be, much of which is controversial. The labella may still show traces of two segments, but they are bulbous, connected by a hyaline membranous middle part which can be swelled by blood pressure. The outer part is better chit- inized and supported by chitinous arcs. Altogether the labella and their supports are incorporated into the functions of the proboscis into which the mouth parts combine. There are cer- tainly many variations in detail but as a whole the principle of a dipteran labium is present from the beginning as far as I am able to find out. The dipterologists agree that these mouth parts are derived from those of the Mecoptera. But the only condition of transition which I can find in Diptera is the rudimentary seg- mentation of the primitive labellum. Thus it looks to me as if the decisive step to “dipterisation” was a single one, whether derived from a Mecopteran type, or if this is a blind side alley, from a more primitive one. It is possible that Ferris laid less stress upon the first establishment of the Dipteran type in his 46 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 “hundreds of transitional stages,” though he starts his series with the Mecoptera as first transitional types. Villee had only spoken of the change of the primitive biting mouth parts (esp. labrum) into the Dipteran type. Probably Ferris alluded to the develop- ment of the specialized types, e.g., in Drosophila, from the prim- itive dipteran type. If one arranges the labella of many types of flies according to e.g., the number of pseudotracheae or the sense organs or the shape, one can certainly put them into a series, though not one of hundreds of steps, and certainly not a phylo- genetic one. It has frequently been pointed out in evolutionary discussions that variable objects may be arranged in a series whenever quantitative variants are involved, but without any meaning in regard to the derivation of one from the other. If we take a crude example; we might arrange all brass instruments into an evolutionary series according to the number of valves or the bending of the tube or the size or all of them together. Is this an evolutionary series? There is certainly no transition between a tuba and a valve instrument. The last phylogenetic step, the saxophone, has probably not been derived from a horn or cornet, but from the constructive principles of some wood wind without any transitions. In the same way the existence of a labellum with one, two, four, many pseudotracheae in different Diptera, specialized for different ways of feeding does not imply that this represents an evolutionary series. Just as some mutation must have once produced the primitive two pseudotracheae from a form without them, also four of them may have originated at once by a different mutation. The same argument applies to all other specializations. Genetics has taught us that in series of multiple alleles of one character showing all transitions, e.g., from large wings to absence of wings, one mutational step may produce the extreme as well as any intermediate. In the case under discussion it has been shown that one mutational step transforms a highly specialized labellum into a segmented ap- pendage. This makes us suspicious of graded series of evolution assembled from numerous variants going in all directions. But these are details. The decisive point is the first step from a biting labium to a sucking one, from a palpus to a labellum. For this I have, thus far, failed to find the numerous transitional steps, though one might say, comparing as types, Periplaneta, Panorpa and primitive fly, that the Mecoptera have gone in the direction APRIL, 1945] GOLDSCHMIDT MOUTH PARTS IN DIPTERA 47 of Diptera in some respects but failed to take the decisive step which I can consider only as a single one. But even if the Mecoptera were the actual ancestors of the Diptera and the two- jointed palpus and rudimentation of glossae and paraglossae and the occasional presence of pseudotracheae (if true) were one of the proofs of this, the flat, biting type of mouth parts, though soft and reduced, is not yet a beginning of a dipteran type which involves the tubular, connected, swellable organ into which men- turn, submentum, as well as the palpi enter by a proper trans- formation (which includes also muscles, sense organs, etc.) which it is not easy to imagine as having occurred in small steps. Literature All papers mentioned in the text but not here cited, are quoted in one of the following papers; the most complete list is found in Crampton (1942). Bridges, C. B. and Th. Dobzhansky 1932. Arch. f. Entwckl. Mech. der Organ. 127:575-590. Crampton, G. C. 1923. Proc. Ent. Soc. Wash. 25:171-180. 1925. Ibid. 27:68-90. 1942. Guide to the Insects of Connecticut, State Geol. Nat. Hist. Surv. Bull. 64(6) :10-131. Ferris, G. F. 1943. Microentomology. 8(l):2-7. Frey, R. 1913. Acta Soc. pro Fauna et Flora Fenn. 37:1-50. 1921. Ibid. 48:1-247. Goldschmidt, R. 1934. Lymantria. Bibl. Gen. 11:1-180. 1940. The material basis of evolution. Yale Press, New Haven. Hendel, F. 1936-37. Diptera, in Handbuch d. Zool. 42:1729-1998. Jobling, B. 1927-28. Bull. Ent. Res. 18:211-236. Peterson, A. 1916. Illinois Biol. Monogr. 3:1-61. Snodgrass, R. C. 1935. Principles of insect morphology. New York. Villee, C. 1942. Amer. Nat. 76:494-506. 48 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 FLYING STAGE OF THE DEER LOUSEFLY, LIPOPTENA DEPRESSA (SAY), IN CALIFORNIA (Diptera, Hippoboscidae) BY JOHN EDWARD HARE University of California, Berkeley Lipoptena depressa (Say) is a common bloodsucking ecto- parasite of deer (genus Odocoileus ) in western North America. As in other Hippoboscidae the females are larviparous, deposit- ing at short intervals single full-grown larvae which immediately pupate. 1 The pupating larvae are smooth and clean, dropping from among the host hairs to the ground where the entire pupal period is passed. At emergence the imago possesses fully devel- oped though fragile wings and flies among the trees in the wood- land haunts of the host. This stage of the parasite, here called the volant, survives but a few days in the absence of the normal host. Upon reaching a deer, the volants immediately crawl be- tween the hairs and begin to suck blood. Here they remain as permanent parasites for the rest of their lives, soon losing the wings by a simple process of wear. In the course of a detailed study of the complete life history of this species over a period of six years, numerous observations have been made of the occurrence and behavior of the volants in California. The present paper is concerned only with the volant phase, i.e., that portion of the life cycle beginning at emergence from the puparium, and the subsequent events which lead to the finding of a host. Little published information exists on the biology of L. dep- ressa, and this almost exclusively concerns the parasitic stage on the deer. Spencer (1939) believed that young flies probably emerge at intervals throughout the spring in British Columbia, basing his conclusions on a study of mature parasites taken from deer carcasses in November. Bequaert (1942) mentions that flights of many winged, newly emerged individuals of both sexes are often observed in the fall, when they frequently alight on people and are said to bite readily. Cowan (1943) states that 1 The gestation period of L. depressa is three to four days as found by expe- riments with captive deer, soon to be reported. Cowan (1943) estimated a two months period; Hei-man ( Calif . Fish & Game, 31 (1),1945) has repeated this figure. APRIL, 1Q4£] HATtE— T.TPOPTENA nEPPlilflRA 49 volants often alighted on his clothing, and from rearing experi- ments on puparia deposited by females removed from dead deer, he concluded that emergence in the wild occurs from June to November in British Columbia. Herman (1945) includes photo- graphs of the volant, puparium and parasitic female of L. dep- ressa, as Neolipoptena ferrisi (Beq.) I have observed and collected free flying volants in California at the following localities : Binkley Ranch, near Kelseyville, Lake County; 17-mile Drive, Carmel, Monterey County; Sespe Gorge, near Ojai, Ventura County; Mt. Diablo, Contra Costa County; Redwood Canyon and Strawberry Canyon, Alameda County. No attempt was made to survey the entire state to establish the geo- graphic limits of distribution, but in general it may be said to coexist with that of the deer hosts. Volants of Neolipoptena ferrisi (Bequaert) ( Lipoptena subu- lata Ferris and Cole) have been collected along with L. depressa on only two occasions (Lake County, Ventura County) and then in very small numbers. N. ferrisi, although it accompanies L. depressa infestations on deer in many parts of California, ap- pears to be more limited in distribution, at least with respect to coastal California. Bequaert (1937, 1942) lists specimens of L. depressa from 29 of the 58 counties of California, from Humboldt, Trinity and Lassen in the north, to Orange, Riverside and San Diego in the south, and from the Pacific Coast to the Sierra Nevada Mountains. The races of Odocoileus hemionus (Mule and Blacktail deer) are widely distributed in California, according to Dixon (1934) and Cowan (1936), and are absent only from the hot interior valleys and from the Great Basin Desert region of southeastern Califor- nia. The presence of infested deer in a given area, as determined by examination of carcasses during the hunting season, would indicate the occurrence of the volant stage in the same general area. Wherever intensive search was made in localities known to be frequented by deer, volants have sooner or later been found. In certain cases, notably Carmel, Mt. Diablo and Strawberry Canyon (Berkeley) , many hundreds of volants have been ob- served and collected at frequent intervals during the warmer months of the year. The conclusions here presented are based on a total of over 70 daily field trips, of which approximately 50 refer to the 50 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 Strawberry Canyon, Alameda County, locality, which served as the primary field station for the observation of wild volants. Seasonal Occurrence My earliest records for the year for the appearance of L. dep - ressa volants are: March 26, 1941, 35 flies, Mt. Diablo; March 28, 1942, 24 flies, Mt. Diablo; March 18, 1944, 3 flies, Berkeley hills. Trips made to these localities during January and Febru- ary of several years were negative. From March onward the volants appear in ever-increasing numbers as the weather grows warmer, until a peak is reached in the latter part of July, at which time as many as 200 flies have been caught in one hour, in an area of one acre. In the Berkeley station, for which I have the most complete records, the volant population appears to diminish during the months of August and September. Volants continue to occur in fairly good numbers on warm days in October and November, and four flies were caught flying as late as December 8, 1943. Volants have also been collected in August in Ventura County, September in Lake County, and October in Monterey County. On October 5, 1938, the flies were exceedingly numerous along 17-Mile Drive, Monterey County, and over 500 specimens were collected by three collectors in less than two hours. This indicates that the seasonal peak may extend into late fall in some localities. Volant and Host Ecology It is to be expected that the ecological niche of the volant stage of L. depressa integrates with that of the host, since this stage of the cycle is devoted entirely to bringing it, fresh from emergence from the puparium in the forest floor, into contact with its host. Bequaert (1942) gives the following as the normal, breeding hosts of Lipoptena depressa: Odocoileus hemionus hemionus (Rafinesque) — Rocky Mountain Mule Deer; O. h. columbianus (Richardson) — Columbian Blacktail Deer; Odocoileus virgini- anus leucurus (Douglas) — Western White-tailed Deer; Cervus canadensis (Erxleben) — the Wapiti or American Elk. The nor- mal ecological pattern in California concerns races of Odocoileus hemionus only. Bequaert’s list of specimens examined includes a record from Odocoileus hemionus calif ornicus (Caton), and APRIL, 1945 ] HAKK — LIFOrTKHA UEritESBA 51 in the absence of host identification of many other series of specimens, the localities given would indicate that 0. h. inyoensis Cowan and 0. h. fuligirmtus Cowan may also be normal hosts of L. depressa (based on Cowan’s study of the distribution of Pacific Coast Deer, 1936) . The only California race of Odocoileus hemionus for which there seems to be no evidence, direct or in- direct, of infestation by L. depressa, is 0. h. eremicus (Mearns) , the Burro Deer. According to Cowan, this race is found in Cali- fornia only in the extreme southeastern corner of the state, in the Lower Sonoran life-zone, chiefly below 1500 feet. This race of deer is isolated from the coastal races by the Colorado Desert, and has habits which are different from the hemionus Rassenkreis as a whole. Blacktail deer in California inhabit mainly the Transition and Boreal zones, but are also abundant in the Upper Sonoran chaparral belt of the coastal region, from Mendocino County southward. Cowan states that in the coastal regions the habitats favored are Redwood, Scrub Oak, and chaparral, while in the Sierran region the foothill chaparral belt and the Yellow Pine-chaparral association support the bulk of the population. Dixon (1934) considers California Mule Deer to be characteristic inhabitants of the Yellow Pine and White Fir forests in the cen- tral Sierran region, and has observed herds at elevations up to 11,000 feet. From the above account it may be concluded that deer are to be found under a wide variety of floristic conditions, at all ele- vations up to at least 10,000 feet, and absent only from the most arid portions of the Lower Sonoran zone (cf. Grinnell, 1939). At the collecting localities mentioned above, volants of L. depressa were collected in a number of different plant associa- tions: Digger Pine, Pinus sabiniana, Lake County; Monterey Pine, Pinus radiata, mature growth — Monterey County, young growth — Alameda and Contra Costa counties; Cedar, Chamae- cy paris thyoides, young plantings, Strawberry Canyon, Alameda County; Redwood, Sequoia sempervirens, Redwood Canyon, Ala- meda County; Pine-Oak-Juniper association ( Pinus sabiniana- Quercus douglasii-Juniperus californica ) Mt. Diablo, Juniper Camp, Contra Costa County; Laurel-Oak association ( Umbellu - laria calif ornica-Quercus agrifolia ) Redwood Canyon; Willow- wild rose thicket (Riparian mountain meadow) Ventura County. The volant habitats are all mesophytic in nature, when con- 52 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 trasted with the adjoining grassland and chaparral formations usually present at the same localities, but which are almost uni- versally negative with respect to volants. Among the factors which appear to be important are, 1) moderate to dense shade (which directly modifies the temperature relations and the evap- oration rate) and 2) shelter from wind. The shade factor is also involved in the production of a light-shade edge pattern which is commonly present in the volant habitats. The ecological rela- tions of the light-shade edge will be discussed later. Deer beds and other fresh sign were commonly present in the same vicinities as the highest volant densities. The highly local- ized occurrence of volants in these areas suggests that the flight range is quite limited. In localities where the volants are habitually present, and during the warmer hours of the day, considerably more flies can be caught on the body of the collector than in a net. It is more accurate to say that the flies seek out the collector than the reverse. The volants have the habit of alighting suddenly on almost any part of the body, clothed or exposed. Here they pause for a fraction to several seconds, and then just as suddenly fly off again. By acting quickly, it is possible to capture the flies while they remain on the skin or clothing, by grasping them lightly between the fingers, or by inverting a collecting tube over them. The volants are small (3 mm.) flat, brown flies, with tough leathery bodies which can withstand considerable pressure and handling without injury, other than occasional tearing of the delicate wings. Localities were surveyed simply by traversing, meanwhile be- ing on the alert for any volants which might alight on the body. Specimens were obtained in this way even when the population density was so low that continuous beating for long periods did not yield a single fly by the conventional method. Sweeping and beating were useful during cold or wet weather or in the very early morning hours, when inactive or sluggish volants could be swept from edge foliage of trees, shrubs or grass in the same localities. Of a total of over 600 individually recorded observations on volant behavior, approximately 17 per cent alighted on my body while I stood or moved in direct sunlight, another 17 per cent while in deep shade, and the balance, 66 per cent, occurred in or APKIL., I^45J IIAR LirOl’TIiNA Uizrn ESSA 53 close to the interzone produced at the edge of the distinct shadow cast by the trees which border the woodland formations. The occurrence of volants at this light-shade edge was very character- istic, and the highest frequencies of landings always took place here. Landings were most numerous when moving from shad- ows outward to bright sunlight, less when moving along the shadow edge, and least when moving from sunlight into shadow at right angles to shadow edge. A similar behavior has been reported for the volants of Lipoptena cervi in Germany, by Schroeder (1911) who describes how over 100 specimens were caught as they alighted on several people crossing a clearing in a forest in Pomerania, in October. No details were given by Schroeder, but to collect that number of volants by hand requires time and care, and one may assume that the members of his party moved about the clearing while awaiting the flies. The behavior of L. depressa volants may be attributed to the interaction of a number of responses, which probably include a phototaxis, form vision and light adaptation, and perhaps also detection of moving objects. Experiments have been conducted on the photic responses and other orientations of the volants, as well as on newly established and old feeding flies, and these will be reported in a later paper. It is interesting to note that the behavior of tsetse flies, which in many ways are ecologically equivalent to the volant L. dep- ressa, resembles closely that described above. Schwetz (1919) states that Glossina fusca Walker occurred almost exclusively along paths and roads bordering forests. G. palpalis R.-D. ac- cording to Fiske (1920), when in search of a host, follows game trails, lake shores and stream banks, and in general follows the line between shadow and sunlight, being averse to penetrating shadow where light is not evident beyond, and vice versa. Swynnerton (1936) describes the “vegetational concurrence” required by G. morsitans Westw. for example, which requires both a savannah of sufficient shade value, and open glades in which to hunt prey. The feeding grounds are on sections of paths or glades and passes between thickets. Jackson speaks of the same species (1941) living in restricted “ambits”, congregating along the “contact line of woodland and swamp, often in a special interzone including trees not found in either of the other types”. 54 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 He states that the interzone provides good visibility and attractive conditions for the hosts, while the shadier woodland offers breed- ing and resting haunts. The habits of the hosts of L. depressa, so far as they are known, fit into the volant pattern very well. Dixon (1934) states that mule deer in California spend the middle of the day bedded down in cool secluded nooks, such as groves of pines provide. Other bedding places are wild plum thickets, rocky ridges and hemlock thickets. To reach these spots, the deer must travel from the early morning feeding grounds in meadows and chaparral- covered hillsides, traversing patches of woodlands and the forest edges on the way. Here the volants have adequate opportunity to alight on the slowly moving or even momentarily stationary deer still browsing as they go. The bedding-down places are usually close to the forest edge, as the wary animals prefer a spot with an unobstructed view on one or two sides. In late fall and winter sunny nooks are sought for sun baths (Dixon, 1934, p. 35). As the shadows shift, the deer change their position, and move to other sun-bathed spots. This is precisely where volants habitually occur. The responses to temperature are also condu- cive to the rendezvous. Volants tend to retire into the deeper shadows on the warmest summer days, but on cool spring and fall days, the flies congregate in the warm sunny glades bounded by dense shadows. I have found by personal experience with cap- tive blacktail deer that these animals are extremely light-shy on hot summer days, and seek the cool shadows whenever permitted. The reverse is true in cool weather. Diurnal Cycle During the night and in the first hours after dawn, volants may be recovered from foliage in the same localities where flights are made during the day. Crawling activity evidently be- gins as soon as light is present, when the temperature permits sluggish movement. Sluggish volants, their bodies wet with dew, have been observed dropping from branches of trees overhead as early as 5 A.M., just before dawn, on a cool foggy morning (13° C.). Volants kept at 10° C. overnight, move the legs and attempt to crawl almost immediately when brought into light. Flights have been observed as early as 6:30 A.M. (still air temperature in this particular case was 18.0° C.) when the sun APRIT., 1Q4.E] HARE— LTPOPTENA DEPRESfiA 55 was one hour above the horizon. The volants are also active on days with low fog, temperature permitting. The coolest condi- tions under which volants were seen flying, were recorded on December 1, 1943. From 1:20 P.M. to 2:30 P.M. the shade air temperature was 12.7—13.0° C. while the sunny air temperature was 18.5-23.0° C. Six volants were caught alighting on my body during this time. On another occasion, flight was slow and clumsy at 14-17° C., on a day with a low fog, which excluded the possibility of a warming effect by direct sunlight. The flies were seen to vibrate their wings several times before taking off in flight. This does not happen on warmer days, and suggests that under the cooler conditions, it is necessary for the volants to raise the internal temperature for proper function of the flight muscles, as pointed out by Wigglesworth (1939, p. 90) for other insects. Optimum range of temperature for flight under field condi- tions appears to be 18-24° C. When the shade air temperature exceeds 25° C. the number of flies appearing at the forest edge decreases, as compared with average numbers caught on cooler days. The few flies present tend to remain in the deep shade, where they continue flying and resting activities. A similar type of reaction has been described for Glossina morsitans by Jack and Williams (1937) who found that as the temperature rises above 32° C. the response to light changes from photopositive to photonegative. They also showed that lowering the humidity lowers the threshold for this change in photic response. Volants continue to make short flights throughout the day, frequently alighting on trunks and branches of trees, foliage and grass, where they rest briefly, and fly off again. One receives the impression of almost constant activity on the part of the flies. This restless behavior continues when the volants are put into dry collecting vials, where rapid crawling and flying still occur. Only with the coming of darkness and a drop in temperature does volant activity cease. Those flies surviving a longer period of starvation remain inactive on vegetation for the night and resume the search for a host the following day. Cowan (1943) kept seven newly emerged volants of L. dep- ressa over damp sand at room temperature. The maximum period of survival was 72 hours, average 57 hours. I have conducted 56 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 numerous survival experiments with reared as well as wild volants, and a brief summary of results will be given. Volants of L. depressa lived from one to eight days after emergence from the puparium. The maximum survival was ob- tained Avith a group of reared flies emerging from normal puparia collected from captive deer. A total of twenty emergents were kept in small (20x6 mm.) vials plugged with cotton, in normal laboratory daylight, at room temperature and humidity: 50 per cent mortality at 4% days, maximum survival, 1 fly 8 days. Wild caught volants, kept at 84 per cent relative humidity and 22.0-22.8° C. lived up to 3 Yz days, 50 per cent mortality at 1% days, when kept under daylight conditions; when kept in dark cabinet, other conditions same, wild volants lived up to 6 days, 50 per cent mortality at 3% days. At 98 per cent R. H. and 16-19° C. wild volants lived up to 6 days, 50 per cent mortality at 4 days, when kept in dark cabinet. Lowering the humidity in- creases the mortality rate and shortens the maximum survival time. At room temperature and humidity, 75 per cent of wild volants kept in large glass jars die the first day. Factors which decrease the activities of the flies, hence the energy expended, tend to increase the maximum survival time and to lower the mortality rate. Such factors include: limiting the space for walk- ing and flying, cutting down or excluding light, and lowering the temperature. A similar relationship was found for Pseudo- lynchia canariensis (Macq.) [ P . maura (Bigot) ] by Prouty and Coatney (1934), where longevity without food was 77-109 hours in direct proportion to the energy used up in activity. Under natural conditions, the volant L. depressa may be ex- pected to live and remain active for one to four days. Rearing experiments with captive deer indicate that 50 per cent of those volants still fairly active 4 days after emergence, can successfully establish on the host. One-day-old flies are 75 per cent successful. Literature Cited Bequaert, J. 1937. Notes on Hippoboscidae. 5. The American species of Lipoptena. Bull. Brooklyn Ent. Soc. 32:91-101. 1942. A Monograph of the Melophaginae or Kedflies of sheep, goats, deer and antelopes. Ent. Amer. 22:1-220. APRIL, 1945 ] II A It LIPOrTENA DI^PRESSA 57 Cowan, I. McT. 1936. Distribution and Variation in Deer ( Odocoileus ) of the Pacific Coastal Region of North America. Calif. Fish and Game, 22:155-246. 1943. Notes on the Life History and Morphology of Cephen- omyia jellisoni Townsend and Lipoptena depressa Say. Canad. Journ. Res. 21:171-187. Dixon, J. S. 1934. A study of the life history and food habits of Mule Deer in California. Calif. Fish and Game, 20:181-282, 315-354. Fiske, W. F. 1920. Investigations into the Bionomics of Glossina palpalis. Bull. Ent. Res. 10:347-463. Grinnell, J. 1935. A revised life-zone map of California. Univ. Calif. Publ. Zool. 40:327-330. Jack, R. W. and W. L, Williams 1937. The effect of temperature on the reaction of Glossina morsitans Westw. to light. Bull. Ent. Res. 28:499-503. Jackson, C. H. N. 1941. Economy of a tsetse fly ( G . morsitans ) population. Bull. Ent. Res. 32:53-55. Kinghorn, A. 1911. Report on Human Trypanosomiasis in Ashanti (ms.). Bull. Sleeping Sickness Bur. 3:133. quoted in Newstead, 1924. Newstead, R., A. Evans and W. H. Potts 1924. Guide to the study of Tsetse flies. Memoir (N.S.) no. 1, Liverpool School of Tropical Medicine, 332 pp. Prouty, M. J. and G. R. Coatney 1934. Further studies on the biology of Pseudolynchia maura (Bigot). Parasitology, 26:249-258. SCHROEDER, G. 1911. Beitrage zur Dipteren-Fauna Pommerns. Stett. Ent. Ztg., 72:367. SCHWETZ, J. 1918. A comparative study of the habits of Glossina brevi- palpis Newstead, G. fusca Westw., and G. pallidipes Austen, in the Belgian Congo. Ann. Trop. Med. Paras. 11:365-398. Spencer, G. J. 1939. Ectoparasites of Deer in British Columbia. Proc. Ent. Soc. Brit. Columbia. 35:15-19. SWYNNERTON, C. F. M. 1936. The Tsetse Flies of East Africa. Trans. Roy. Ent. Soc. London, 84:1-579. WlGGLESWORTH, V. B. 1939. Principles of Insect Physiology. E. P. Dutton and Co., New York. 58 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 FIVE NEW SPECIES OF ALEYRODIDAE FROM CALIFORNIA (Homoptera) BY W. W. SAMPSON University of California, Berkeley Among the Aleyrodidae collected by the writer in California are five species whose characters do not resemble those of other described forms. These apparently new species are described herein. Holotypes and certain paratypes will be deposited in the California Academy of Sciences. Fig. 1. Aleyrodes osmaroniae Sampson. A, pupal case. B, vasi- form orifice. C, margin of case. Genus Aleyrodes Latreille, 1810 Aleyrodes osmaroniae Sampson, new species (Fig. 1) Pupal case. Size 1.28 mm. long by 0.97 mm. wide; shape broadly elliptical; margin slightly irregular, chitinized for a width of 0.35 mm.; behind the chitinized margin there occurs for some distance groups of dotted areas; vasiform orifice subcordate and striated, the posterior margin pointed, operculum roundly trape- AI-KIL, 1945] SAMrSON ALEYEODIDAE 59 zoidal, setose, lingular three-quarters the length of orifice, the two setae projecting beyond the margin of the orifice; caudal margin of body slightly indented and bearing two setae. Color of case bright lemon yellow; without wax secretion. Adults. N ot known. Collected by the writer from Osmaronia cerasiformia in Strawberry Creek Canyon, on the Campus of the University of California, Berkeley, California, June 14, 1941, along with A. spiraeoides (Q.) from the underside of the leaf. This species differs essentially from Aleyrodes spiraeoides (Quaintance) by having the chitinized margin. Fig. 2. Tetralicia ceanothi Sampson. A, pupal case. B, vasi- form orifice. C, margin of case. D, apparent margin of case. Genus Tetralicia Harrison, 1917 Tetralicia ceanothi Sampson, new species (Fig. 2) Pupal case. Size 0.623 mm. long by 0.540 mm. wide; shape broadly ovate, narrowing posteriorly; margin toothed, eight teeth in 0.0783 mm. wax tubes well developed; deflexed portion of case about one-fourth the width of case, 0.0703 mm. wide; apparent margin bears bidentate projections, which are the two rows of imbrications running over the edge to the deflexed portion; there are about 88 of these double rows of imbrications, which extend from the edges of the faintly indicated body segments to the margin; a few single imbrications are scattered over the dorsum; thoracic transverse slit not reaching apparent edge of body; vasi- form orifice subcordate, set in a roundly rectangular, chitinized area; operculum subcordate, nearly filling orifices; lingula hidden; 60 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 posterior prolongation slightly developed, bearing two long setae. Case black, resting on a small amorphous mass of wax. Adults. Not known. Collected by Nathan Stahler and Thomas Kelly from Cean- othus cuniatus near Bishop, California, March 29, 1940. This species is related to Tetralicia nigrans (Bemis), but dif- fers essentially from it by having the wide chitinized area around the vasiform orifice and by having imbrications on the dorsum. Fig. 3. Tetralicia sierrae Sampson. A, pupal case. B, vasi- form orifice. C, margin of case. D, apparent margin of case. Tetralicia sierrae Sampson, new species (Fig. 3) Pupal case. Size 0.820 mm. long by 0.450 mm. wide; shape elliptical; margin toothed, four teeth in 0.117 mm.; deflexed por- tion of case about one-third the width of case, 0.0783 mm. wide; apparent margin bearing bidentate projections with a smaller one in between each, the projections being the appearance of double rows of granules on the edge of the deflexed portion; the granules are lacking in the medium line of the dorsum; thoracic transverse slit reaching edge of apparent margin; vasiform orifice cordate, raised, slightly longer than wide; operculum, cordate, filling ori- fice; lingula hidden; posterior prolongation well developed, bearing two long setae. Gase black, with a thin fringe of wax. Adults. Not known. Collected by the writer from an undetermined, low spreading shrub at Truckee, California, June 25, 1940. This species is related to T . ceanothi, but differs essentially from it by having the case granulate and by not having the wide chitinized area around the vasiform orifice. Ai'iUL, 1945] SAMrSON ALEYRODIDAE 61 Genus Trialeurodes Cockerell, 1902 Trialeurodes califomiensis Sampson, new species (Fig. 4) Pupal case. Size 1.07 mm. long by 0.74 mm. wide; shape broadly elliptical; margin entire, slightly irregular, with a few faint folds behind it; a single row of long pointed papillae lie behind the margin, nine in 0.16 mm.; behind the papillae are one or two rows of tiny clear pores, some of which are doubled, the same type of pores occur along each side of the abdominal ridge, one to each segment, and another row further out, as well as a few on the Fig. 4. Trialeurodes califomiensis Sampson. A, pupal case. B, vasiform orifice. C, margin of case. thorax; vasiform orifice subcordate; operculum rounded, filling about half of the orifice; lingula trilobed on each side, without setae nearly reaching to posterior margin of orifice; caudal furrow indicated; two pairs of hairs are located on the posterior margin. Case black, with a fringe of wax up to one-half the width of case, dorsum without wax; case slightly elevated above wax fringe. Appears very much like immature forms of Tetraleurodes stanfordi ( B emis ) . Adults. Not known. Collected by Dr. M. A. Cazier at Guerneville, California, March 15, 1939, and at Antioch, California, by E. A. Drews and by W. W. Sampson, April 8, 1940, from Quercus sp. This species differs essentially from Trialeurodes wellmanae 62 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 (Bemis) by being black and lacking the large semi-transparent areas on the cephalo -thorax. Trialeurodes drewsi Sampson, new species (Fig. 5) Pupal case. Size 0.78 mm. long by 0.48 mm. wide; shape nar- rowly elliptical; margin regularly crenulate, five crenulations in 0.157 mm.; an irregular row of small papillae occurs behind the margin, along with a few larger in size but fewer in number; dorsum bearing about nine pairs of stomata-like pores on the central portion, and two pairs of small papillae toward the lateral ends of the transverse thoracic slit and a larger pair on the cephalo-thorax ; vasiform orifice subcordate, ribbed; operculum Fig. 5. Trialeurodes drewsi Sampson. A, pupal case. B, vasi- form orifice. C, margin of case. D, stomata-like pore. elongately trapezoidal, narrowing posteriorly, filling slightly more than half of the orifice; lingula nearly reaching the edge of orifice, trilobed on each side, and without setae; two setae much longer than the vasiform orifice occur near the orifice, and two near the caudal margin of the case. Case black, greatly elevated on a palisade of white wax; dorsum covered with a layer of clear wax bearing numerous spines of clear wax. Adults. Not known. Collected by the writer from Quercus sp. at Mt. Tamalpais, Marin County, California, March 16, 1941. This species is related to Trialeurodes tentaculatus (Bemis), from which it differs by being black in color and having the stomata-like pores. APRIL,, 1945 ] SEBV£RS TKIC.HOrS.E.NIINAIS 63 NEW GENERA AND SPECIES OF TRICHOPSENIINAE FROM AMERICAN AND AUSTRALIAN TERMITE NESTS (Coleoptera, Staphylinidae) BY CHARLES H. SEEVERS Research Associate, Chicago Natural History Museum The staphylinid beetles of the subfamily Trichopseniinae con- stitute a small but very interesting element of the alien insect fauna inhabiting termite ' colonies. Among the termitophilus beetles they are notable chiefly because of their association with the more primitive termites, and for their wide geographic range which includes both hemispheres. The great majority of groups of termitophilous insects are restricted to one hemisphere or the other, but the thirteen known Trichopseniine species were found in Argentina, British Guiana, the United States, Java, Sumatra, and Australia. The intent of this paper is to describe the new forms which have been acquired since an earlier report 1 in which I proposed that the Trichopseniinae be given subfamily status because of their distinctive metasternal structure, hind-leg articulation, and male genitalia. The most noteworthy addition to the subfamily is its first Australian representative, the bizarre genus, Mastopsenius. The peculiar facies of Mastopsenius scarcely indicates relationship to Trichopsenius, but this is in line with the subfamily tendency for each genus to develop its own distinctive habitus. The diversity within the group is more apparent than real for in most respects the basic morphological features are rather similar. The host relationship of Mastopsenius is especially interesting, for its host, Mastotermes darwiniensis Froggatt, is the most primitive of present-day termites, and sole living representative of the family Mastotermitidae, while the other Trichopseniinae are guests of the Rhinotermitidae. With more material available for study, it is now evident that the North American genus Trichopsenius is comprised of at least 1 Seevers, C. H. 1941. Taxonomic investigations of some termitophilous Sta- phylinidae of the subfamilies Aleocharinae and Trichopseniinae (new subfamily). Ann. Ent. Soc, Amer., 34 :318-349, 3 pi. 54 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 2 four species instead of one. The literature records Trichopsenius depressus Leconte as ranging from Massachusetts to California, but closer study shows that all of the specimens are not con- specific. It is clear, also, that some degree of host specificity exists, and that each species of Trichopsenius is restricted to one or a few species of Reticulitermes. The staphylinid beetle, Schizelythron javanicum Kemner * 2 , collected from the nest of Schedorhinotermes javanicus Kemner, at Buitenzorg, Java, should be included in the Trichop seniinae rather than in the Aleocharinae where placed by Scheerpeltz 3 . Although I have not seen this species, I have no doubt of its re- lationships; the distinctive Trichopseniine metasternal and hind- leg characters are plainly evident in Kemner’s illustrations. Schizelythron derives its name from a remarkable character ; each elytron is split lengthwise from near the base to the apex, and the lateral half diverges strongly from the medial part. I am very grateful to Dr. A. E. Emerson for determining the host termites cited in the paper, and to the following men for the gift of specimens or for arranging loans: Dr. R. E. Blackwelder of the United States National Museum, Dr. M. F. Day, Dr. Emer- son, Mr. C. A. Frost, and Dr. M. W. Sanderson of the Illinois Natural History Survey. Mastopsenius Seevers, new genus Body robust, fusiform; sparsely setose; head moderately de- flexed, compressed; clypeus very short; antennae elongated, an- tennomeres 3-9 campanulate; eyes large; gula sclerotized; mentum strongly transverse, sides rounded, apex emarginate; ligula bifid; labial palpi 3-segmented (third segment bearing a tiny spicule), its second segment elongated and with sides subparallel, the slen- der third segment articulating with its apex; maxillary palpi 4- segmented, the slender second segment increasing uniformly in width distally, the fourth segment narrowly conical, without a terminal spicule. Pronotum robust, strongly transverse, anterior and lateral bor- ders margined, basal border margined only along outer one-fourth; surface of pronotum strongly deflexed at base (medially) forming a conspicuous posterior “face” of the pronotum; elytra narrower than pronotum, sides and apical margin uniformly rounded, apical - Kemner, N. A. 1925. Javanische termitophilen I : Schizelythron javanicus n. g., n. sp., eine neue physogastric Staphylinide von einem neuen, nicht zu den Aleochariden gehorigen Typus, nebst biologischen Bemerkungen uber Jacobsonella termitobia Silv. Ent. Tidskr., 46:107-126, 1 pi. 3 Scheerpeltz, O. 1934. Staphylinidae VIII. Coleopt. Cat. 130 : 1501-1881. APRIL, 1S>45 J SEEVEBS 'i'«X the first segment with nine short, stout spurs along anterior and basal margins and with longer bristles distally. Pronotum half again as broad as long and about one-fourth broader than head. Mesonotal pads as long as pronotum, each pad about one-fifth narrower than length of pronotum or mesonotal pad. Elevated area of prosternum a little longer than broad at base, the anterior margin with seven very stout bristles laterally. Elsewhere on anterior half with longer, more slender bristles and with shorter bristles posteriorly on the disk, especially laterally (a few of the central ones apparently broken off). Metasternum with numerous very fine bristles near posterior and lateral mar- gins. Metapleurites with eight or nine irregularly directed, stout bristles arranged in two or three ill-defined rows. Size: male 3.44 mm., female 3.86 mm. Holotype, female, Lassance, Brazil, April 13, 1935, Em- manuel Dias, collector, C. L. prep. Allotype, male, Sitin DU Matto, Bahia, Brazil, April 13, 1935, Emmanuel Dias, collec- tor, C. L. prep. Nearest to longiceps with which it agrees in absence of gular bristles, in its exceedingly long labrum, its relatively long, nar- row head and dense bristles posteriorly on metasternum. It differs from longiceps in its smaller size, its more numerous and differently arranged metapleural bristles and the narrower head anteriorly with larger labrum. Hesperoctenes parvulus Ferris and Usinger, new species Head (including labrum) as long as broad; labrum less than three times as broad as length on median line, 8::3 (almost 4 times as broad as long in cartus, 21%::5%, and over four times as broad, 19M>::4, in vicinus ) . Genal ctenidia as seen from above rather strongly rounded immediately behind first antennal seg- ment, following lateral margins of head posteriorly and laterally, the teeth scarcely exceeding sides of head. Gular bristles seven or eight in number, with two of these near the center set slightly forward. Proportion of antennal segments one to four as 2% :4:3% :3%, with seven stout spurs on outer anterior side of first segment beneath. 124 PAN-PACIFIC ENTOMOLOGIST [vOL. XXI, NO. 4 Pronotum slightly more than half again as broad as long, 3::2 a /4, much as in cartus. Mesonotal lobes scarcely shorter than pronotum, a single lobe being one-fifth longer than broad. Elevated portion of prosternum about as long as broad, the disk with five very stout bristles laterally on anterior margin and twenty-six more slender bristles arranged roughly into three rows anteriorly. Behind these the disk is almost entirely naked except for about one dozen small bristles laterally on apical half. Metasternal bristles confined to the areas immediately adjacent to posterior and lateral margins. Metapleurites with only six or eight very stout bristles irregularly arranged into two rows. Chaetotaxy of upper surface of entire body much as in cartus. Size: female 2.28 mm. Holotype, female, Sta. Maria de Epire, Guarico, Venezuela, September, 1937, Pablo J. Anduze, received from Dr. J. Bequaert. The specimen was taken from Glossophaga longirostris Miller, a bat belonging to the family Phyllostomidae. A second female from the same locality on “Vampire bat,” 1936, appears to be slightly teneral. It differs in its slightly larger size, 2.4 mm., and in possessing only 5 gular bristles arranged in an irregular row. Closest to cartus and clearly a member of the compact cartus- vicinus group, having bristles at middle of hind margin of head beneath and very sparsely placed bristles over the entire dorsal surface. The head is as long as broad and the gular bristles are 8 in number arranged in an irregular, almost double row, thus resembling cartus. Vicinus has a shorter, broader head and fewer bristles arranged in a single row. The elevated portion of pros- ternum is naked at middle with only a few bristles posteriorly and laterally, thus still more closely resembling cartus with which it likewise agrees in chaetotaxy of metapleurites. The most distinctive feature of parvulus is the relatively longer and nar- rower labrum. In addition, parvulus is about two-thirds of a millimeter smaller than cartus, the female holotype being the smallest Hesperoctenes as yet described. THE CHAMBERLIN COLLECTION OF BUPRESTIDAE The California Academy of Sciences has acquired the Collec- tion of Buprestidae of Dr. W. J. Chamberlin, of Corvalis, Ore- gon. — Edwin C. Van Dyke. OCT. 1945] MAO— CARDIOCHILES 125 SYNOPSIS OF THE MEXICAN SPECIES OF CARDIOCHILES NEES (Hymenoptera, Braconidae) BY YING-TOU MAO University of California, Berkeley The Mexican species of Cardiochiles were first treated by Cresson in 1873, five species being described; and Szepligeti in 1902 described another species from Mexico. Including the two new species here described there are, therefore, eight Mexican species known to science. They may be separated by the follow- ing table: 1. Eyes bare 2 - Eyes hairy 3 2. Head, thorax, abdomen and legs entirely black ....noctis, new sp. - Thorax in part, abdomen entirely, and legs more or less red bicolor (Szepligeti) 3. Head and thorax more or less yellowish or ferruginous 4 - Head and thorax entirely black 5 4. Stigma brownish-yellow; wings yellowish; coxae yellow, poste- rior parts with black markings; scape lemon-yellow; face punc- tate ornatus (Cresson) - Stigma blackish; wings dark fuliginous; coxae black; scape black; face smooth and polished thoracicus (Cresson) 5. Wings hyaline on basal half, fuliginous on apical half mexicanus (Cresson) - Wings entirely fuliginous 6 6. Malar furrow about as long as the basal width of the mandi- ble; hind femora and tibiae red longimala, new species - Malar furrow not nearly as long as the basal width of the mandible; hind femora and tibiae black 7 7. Fore tarsus and middle tarsus with fifth segment longer and thicker than the second; fore femur and tibia largely black aethiops ( Cresson) - Fore tarsus with second and fifth segments about equal; mid- dle tarsus with second segment longer than the fifth; fore femur and tibia largely brownish-yellow orizabae (Cresson) Cardiochiles aethiops (Cresson), new combination Toxoneuron aethiops Cresson, 1873, Canad. Ent., 5:66-67, $. The following redescription is from the type. 126 PAN-PACIFIC ENTOMOLOGIST [ VOL. XXI, NO. 4 Female. Length 5.5 mm. Black; pedicel, fore femur and fore tibia apically, and last four segments of fore tarsus yellowish brown; wings fuliginous. Head. Antennae incomplete; scape and pedicel with slightly longer pubescence than the flagellum; eyes hairy; ocelli elevated, the distance between the two posterior ocelli slightly longer than that between either of these and the anterior ocellus, and the area around them depressed; vertex smooth and shining; frons impressed, smooth, shining and with a low median longitudinal carina; face smooth, shining and with a short median tubercle above; clypeus smooth, shining and notched on the apical margin medially; temple narrower than the eye in dorsal view; galea short. Thorax. Lateral face of pronotum wrinkled medially; notaulices foveolate; mesoplauron smooth and shining, upper groove rugose in middle portion, lower groove weakly foveolate, the posterior groove foveolate with a smooth impression from the middle leading anteriorly to the lower groove; metapleuron rugose, median ventral part of its anterior portion plain; propodeum rugose, carinae distinct and high, areola dia- mond-shaped, spiracle ovate and situated before the middle of the spiracular area. First abscissa of radius thicker and longer than that of basal vein; third and fourth abscissae of cubitus about equal; second abscissa of cubitus and recurrent vein about equal; interanal vein represented by a pigmented line. Fifth segment of fore leg longer and thicker than second or third; middle leg also with the fifth tarsal segment longer and thicker than the second or third, and tibial spur about as long as the basitarsus; apex of hind tibia not thickened, tibial spur about three-fourths as long as the basitarsus which is shorter than the remaining four segments combined, second tarsal segment slightly longer than the fifth and the third shorter than the fifth, hind claws pectinate basally. Abdomen. First abdominal suture extending obliquely forward laterally; second tergite slightly shorter than the third medially; hypopygium about as long as the second and third tergites com- bined, plowshare-shaped; ovipositor sheath about as long as the first two segments of hind tarsus combined, pubescent. The type female, the only known specimen, is from Cordova, Mexico (Academy of Natural Sciences of Philadelphia). Cardiochiles bicolor (Szepligeti), new combination Toxoneuron bicolor Szepligeti, 1902. Term. Fiizet., 25:78, $. The following is simply a translation of the original descrip- tion. Smooth; head transverse, maxillary palpi 5-, labial palpi 4- segmented; ocelli not located on summit of vertex; eyes bare, occi- put not margined and only slightly excavated. Antenna 42-seg- mented, third segment as long as the obovate scape. Mesonotum oct. 1945] MAO— CARDIOCHILES 127 divided; median lobe broad, not prominent. Propodeum pubescent, areolate. First intercub itus angled, without stump of a vein; third abscissa of radius weakly marked, transparent and arching almost bowlike to the wing tip; anal cell divided; radial cell of hind wing not divided. The longer spur of hind tibia half as long as the metatarsus ; tarsal segments 2-5 much more slender than the the first. First abdominal segment shorter than its apical width, almost triangular, strongly narrowed anteriorly, with two longi- tudinal furrows defining a triangular area; following segments transverse and of about equal length; hypopygium large. Black; mesothorax (except median lobe), scutellum, femur of hind leg, the tibiae (tip of posterior tibia brown), tarsi of fore and middle legs and abdomen, red. Wings brown, stigma dark. Length 9 mm., ovipositor sheath short, wedge-shaped. Mexico. Type in the Hungarian National Museum, Budapest. Cardiochiles longimala, new species Male. Length 5.5 mm. Black; fore femur except base, apical half of middle femur, hind femur, and tibiae except inner apex of hind tibia, ferruginous; tibial spurs dark and those of hind leg dark ferruginous. Head. Antenna 35-segmented; scape and pedi- cel with longer pubescence than the flagellum; eye hairy; ocelli slightly elevated and the distance between two posterior ocelli longer than that between either one of these and the anterior ocellus; vertex smooth, shining, and slightly sloping toward frons; frons impressed, smooth, shining, and with a low median longi- tudinal carina; face smooth, shining, with a low median tubercle above and the median line below slightly elevated; clypeus smooth, slightly shorter than the face, its apical margin notched medi- ally; malar furrow slightly shorter than the basal width of the mandible; temple and eye of about equal width in dorsal view; galea moderate, not conspicuously long. Thorax. Lateral face of pronotum medially rugose; notaulices distinct, smooth; mesopleu- ron smooth and shining, upper groove finely rugose, lower groove finely foveolate, posterior groove foveolate with a smooth curved groove from the middle leading anteriorly to the lower groove; metapleuron rugose, median ventral part of its anterior portion smooth and shining; propodeum rugose, transverse carina low, the other carinae moderately high, spiracle ovate. First abscissa of radius longer and thicker than that of basal vein; fourth abscissa of cubitus slightly less than twice as long as the third; second abscissa of cubitus and recurrent vein about equal; inter- anal vein represented by a pigmented line. Fifth segment of fore tarsus longer than the second; inner spur of middle tibia about three-fourths as long as the basitarsus, second segment of middle tarsus longer than the fifth which is about equal to the third; apex of hind tibia not thickened, inner spur slightly over half as long as the basitarsus, basitarsus about as long as the next three 128 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 tarsal segemnts combined, second tarsal segment longer than the third and third longer than the fifth, hind tarsal claws pectinate basally. Abdomen. First abdominal suture extending obliquely forward laterally; an oblique groove on each side of the second tergite halfway between median line and the margin; third tergite about 1.50 times as long as the second. Type. Male, Guadalajara, Mexico, August 2, 1914 (U. S. National Museum, No. 57295). This species is very similar to C. floridanus (Ashmead) except for the longer malar space. Cardiochiles mexicanus (Cresson), new combination Toxoneuron mexicanum Cresson, 1873. Canad. Ent., 5:66-67, $ $. The following redescription is from the type. Female. Length 7 mm. Black, a spot on outer upper orbit yellowish-brown; about apical 0.40 of fore wing and tip of hind wing fuliginous. Head. Antennae incomplete; scape and pedicel with longer pubescence than the flagellum; eye hairy; ocelli slightly elevated, the distance between the two posterior ocelli longer than that between one of these and the anterior ocellus; vertex slightly sloping toward frons, smooth, shining, and about as long as frons; frons impressed, smooth, shining, and with a low median longitudinal carina; face shining, with a short median tubercle above, and the median line slightly elevated; clypeus shining, plain, notched on apical margin medially; temple and eye of about equal width in dorsal view; galea short. Thorax. Lateral face of pronotum weakly rugose medially; notaulices f oveolate, distinct and deep ; mesopleuron smooth and shining, upper groove flat, weakly rugose, lower groove foveolate, and posterior groove foveolate with a smooth groove from the middle leading anteriorly to the lower groove; metapleuron rugose, median ventral part of its anterior portion shining and plain; prop odeum rugose, carinae moderately high, spiracle transverse. First abscissa of radius slightly longer than that of basal vein; fourth abscissa of cubitus about 1.30 times as long as third; second abscissa of cubitus longer than recurrent vein; interanal vein absent. Fifth segment of fore tarsus longer than the second or third; inner spur of middle tibia slightly shorter than basitarsus, second and fifth segments of middle tarsus about equal, the third shorter than the fifth; apex of hind tibia not thickened, tibial spur about 0.60 as long as the basitarsus, basitarsus shorter than the remaining tarsal segments combined, second segment longer than the fifth, and third and fifth about equal; hind tarsal claws pectinate basally. Abdomen. First abdominal suture extending ob- liquely forward laterally; second tergite slightly shorter than the third medially; hypopygium about as long as the second to fourth oct. 1945] MAO— CARDIOCHILES 129 segments of hind tarsus combined, and plowshare-shaped; oviposi- tor sheath (fig. 1A) about as long as the first two segments of hind tarsus combined, pubescent. Male. Essentially similar to the female. The type female, Cordova, Mexico; and two paratypes, one female and one male, Mexico (Academy of Natural Sciences of Philadelphia) ; the paratype female has second abscissa of cubitus and recurrent about equal. One male, Mexico (U. S. National Museum). Cardiochiles noctis, new species Female. Length 7 mm. Black, outer and upper parts of inner orbit ferruginous; apical half of mandible dark reddish; spur of fore tarsus dark ferruginous; eye grayish-black. Head. Antenna 35-segmented; scape and pedicel shining, with longer pubescence than the flagellum; eye bare; ocelli slightly elevated; vertex shin- ing, and slightly sloping toward frons; frons shining, impressed, and with a median longitudinal carina; face with a short median ridge above, below which there is a more or less triangular eleva- tion; clypeus with its basal margin slightly elevated medially, its aipcal margin truncate and slightly arched inward and not notched; temple and eye about equal in dorsal view; galea short. Thorax. Lateral face of pronotum rugose medially; median lobe of mesonotum with a slight depression along each side of the low median longitudinal elevation; notaulices distinct and foveolate; mesopleuron with upper and lower grooves foveolate, and poste- rior groove rather coarsely foveolate with a smooth depression at the middle anterior to the groove; metapleuron rugose with the median lower part of its anterior portion smooth; propodeum rugose, its carinae high and distinct, and propodeal spiracle ovate and elevated. First abscissa of radius longer and thicker than that of basal vein; third abscissa of radius slightly shorter than fourth; second abscissa of cubitus shorter than recurrent vein; second abscissa of submedius slightly longer than first; interanal vein represented by a short stump continued by a pigmented line. Fifth segment of fore tarsus longer than the second; inner spur of middle tibia about two-thirds as long as basitarsus, second tarsal segment slightly shorter than fifth; outer apical margin of hind tibia thickened, slightly flaring, but not forming a strong proc- ess; inner spur of hind tibia about half as long as basitarsus; basi- tarsus shorter than the next four tarsal segments combined, second tarsal segment longer than the fifth; taral claws pectinate basally. Abdomen. First abdominal suture slightly curved cephalad to the margin; second tergite shorter than the third; hypopygium plow- share-shaped, about as long as the first three tergites combined; ovipositor sheath (fig. IB) with short pubescence except at base, about three-fourths as long as the hypopygium. 130 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 Male. Essentially similar to the female, but the propodeal carinae low or not distinct. Type. Female, Meadow Valley, Mexico. C. H. T. Townsend (U. S. National Museum, No. 57296). Paratypes. Four females and three males apparently collected at the same locality by the same collector. Cardiochiles ornatus (Cresson), new combination Toxoneuron ornatum Cresson, 1873. Canad. Ent., 5:66, 69, $. The following redescription is from the type. Male. Length 6 mm. Head lemon-yellow; thorax and abdomen light brownish-yellow; eye grayish-black; flagellum brown; the following parts black: tubercle on the medium upper part of face; a spot on frons including ocelli, and from this a narrow band ex- tending to summit of each eye and then to occiput; lower part of proepistemum; posterior median margin of lateral face of prono- tum; two broad vittae on median lobe of mesoscutum separated by a narrow median line, and one broad vitta on each lateral lobe of mesoscutum; tegula; mesoscutellum except lateral and posterior margins; a u-shaped band between lower and posterior grooves on upper half of mesopleuron; mesosternum; a large spot and a small one laterally, and a large spot ventrally, on hind coxa; a spot on each side of first tergite posteriorly; tergites 3 to 7 except for narrow apical margins; inner side of hind femur and tibia. Wings yellowish, veins and stigma pale brown, or brownish-yellow. Head. Antennae incomplete; scape and pedicel with longer pubes- cence than the flagellum; eye hairy; ocelli slightly elevated, the distance between the two posterior ocelli longer than that between either one of them and the anterior ocellus; frons impressed, smooth, shining, with a median longitudinal carina; face punctate, slightly depressed medially, and with a short median tubercle above; clypeus punctate, its apical margin notched at the middle; temple broader than the eye in dorsal view; galea short. Thorax. Lateral face of pronotum smooth and shining; notaulices moder- ately foveolate, deep ; mesopleuron shining, upper groove punctate, lower groove weakly foveolate, and posterior groove shallowly foveolate; metapleuron rugose, median ventral part of its anterior portion and anterior part of its posterior portion smooth and shin- ing; prop odeum somewhat plain, all carinae high and distinct and spiracle transverse. First abscissae of radius and basal vein about equal, but the former thicker than the latter; third abscissa of cubitus slightly shorter than the fourth; second abscissa of cubitus and the recurrent vein about equal; inter anal vein absent. First segment of fore tarsus longer than the second; inner spur of middle tibia slightly shorter than basitarsus and fifth tarsal seg- Apex of abdomen and ovipositor sheath of C. mexicanus (A), C. noctis (B), C. orizabae (C). Ovipositor sheath of C. thoraci- cus (D). 132 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 ment longer than second; apex of hind tibia not thickened, its inner spur about three-fourths as long as basitarsus; posterior basitarsus about as long as the other four tarsal segments com- bined, second tarsal segment longer than the fifth, third and fifth about equal; hind tarsal claws pectinate basally. Abdomen. First abdominal suture extending obliquely forward laterally; second tergite about half as long as third. Type male, Cordova, Mexico. The type of this species was not recorded by Cresson, 1916, in “The Cresson Types of Hymenoptera” (Mem. Amer. Ent. Soc., No. 1), but the author found a specimen in the collection of the Academy of Natural Sciences of Philadelphia labeled Toxo neuron ornatum. It fits the description and is considered to be the type. Cardiochiles orizabae (Cresson), new combination Toxoneuron orizabae Cresson, 1873. Canad. Ent., 5:66-67, $. The following redescription is from the type. Male. Length 4.2 mm. Black; fore leg yellowish-brown, coxa trochanters and base of femur black, apex of tibia, tibial spurs and tarsus dark yellowish-brown; knee of middle leg yellowish- brown; wings light fuliginous. Head. Antenna 30-segmented; eye hairy; ocelli slightly elevated; vertex about as long as frons, smooth, shining; frons impressed, smooth, shining, and with a low median longitudinal carina; face smooth, shining, and with a short median tubercle above; clypeus smooth, shining and with its apical margin notched at the middle; temple and eye about equal in dorsal view; galea short. Thorax. Lateral face of pro- notum wrinkled medially on anterior half; notaulices finely foveolate; mesopleuron smooth, shining, upper anil lower grooves finely foveolate, posterior groove coarsely foveolate, with a smooth, curved groove from the middle leading anteriorly to the lower groove; metapleuron rugose, median ventral part of its anterior portion smooth and shining; propodeum rugose, carina moderately distinct and high, spiracle ovate and situated before the middle of the spiracular area. First abscissa of radius longer and thicker than that of basal vein; fourth abscissa of cubitus about 1.50 times as long as the third; second abscissa of cubitus and recur- rent vein about equal; interanal vein represented by a pigmented line. Fifth and second segments of fore tarsus about equal; inner tibial spur of middle leg about as long as basitarsus, second tarsal segment longer than fifth, and third and fifth about equal; apex of hind tibia not thickened, inner tibial spur about two-thirds as long as basitarsus, which is about as long as the next three tarsal segments combined, second tarsal segment longer than the third, and third longer than the fifth; hind tarsal claws pectinate basally. OCT. 1945] MAO — CAEDIOCHILES 133 Abdomen. First abdominal suture extending obliquely forward lat- erally; third tergite slightly over 1.50 times as long as the second. Female. Essentially similar to the male. Hypopygium about as long as the hind basitarsus, plowshare-shaped and its median ventral line folded longitudinally ; ovipositor sheath (fig. 1C) about as long as the first three segments of hind tarsus combined, and pubescent. Type male, Orizaba, Mexico (Academy of Natural Sciences of Philadelphia) ; one female, Cordova, Mexico, F. Knab (U. S. National Museum). Cardiochiles thoracicus (Cresson), new combination Toxoneuron thoracicum Cresson, 1873. Canad. Ent., 5:68, $. Toxoneura thoracica Ashmead, 1894. Proc. Ent. Soc., Wash., 3:49, 51, 2 S. The following redescription is from the type. Female. Length 4.5 mm. Head ferruginous; antenna, lower end of the cheek, and lower end of face between cheek and clypeus black; eye grayish-black; apical margin of clypeus dark ferru- ginous; thorax, abdomen and legs black; pronotum, proepister- num, mesonotum, tegulae, upper part of mesopleuron, apical third of fore femur, and fore tibia and tarsus, ferruginous; wings fuli- ginous. Head. Antennae incomplete, scape and pedicel with longer pubescence than the flagellum; eye hairy, ocelli elevated; vertex smooth, polished, and flat; frons smooth, polished, distinctly im- pressed, and with a median longitudinal carina; face slightly less than twice as wide as long, smooth, polished, its median line slightly elevated, and with a very indistinct short median ridge above; clypeus about 1.50 times as wide as long, smooth, polished, and notched on apical margin at the middle; temple broader than the eye in dorsal view; malar furrow about 0.75 as long as the basal width of mandible; galea short. Thorax. Median portion of the lateral face of pronotum rugose; median lobe of mesoscutum without a longitudinal impression on each side of the median line; notaulices foveolate; mesopleuron smooth, polished, its upper and lower grooves foveolate and its posterior groove rather coarsely foveolate with a short smooth impression from the middle leading to the lower groove; anterior portion of metapleuron smooth and polished and posterior portion rugose, anterior half plain; pro- podeum rugose, carinae high and distinct, and spiracle ovate, situated before the middle of the spiracular area. First abscissa of radius 1.50 times as long as that of basal vein; third abscissa of cubitus shorter than the fourth; recurrent vein slightly longer than the second abscissa of cubitus and about one-half as long as the second abscissa of basal vein; nervulus postf ureal by about 0.33 its own length; interanal vein absent. Second and fifth seg- ments of fore tarsus about equal; apex of hind tibia not thickened 134 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 and expanded into a flaring process; inner spur of middle tibia longer than the basitarsus, second and fifth tarsal segment about equal; inner spur of hind tibia about 0.80 as long as the basi- tarsus, basitarsus shorter than the last four tarsal segments com- bined, and second and third tarsal segments longer than the fifth; hind claws pectinate basally. Abdomen, First abdominal suture extending obliquely forward laterally; second tergite slightly shorter than the third medially; ovipositor sheath (fig. ID) about 0.67 as long as the abdomen. Male. Essentially similar to the female; a transverse black band on vertex between eyes; clypeus notched rather strongly. Type female, Cordova, Mexico, and a male labeled Mexico (Academy of Natural Sciences of Philadelphia). One male from Arizona recorded by Ashmead is not in the U. S. National Museum collection. NESTING HABITS OF ANDRENA RHODOTRICHA LINSLEY (Hymenoptera-Andrenidae) Andrena rhodotricha was originally described from specimens collected by G. E. Bohart and the writer at Berkeley, California 1 . It has subsequently been taken by C. D. Michener on Salix. On March 14, 1939, this species was found nesting in a perpendicu- lar five foot bank on the south side of Dwight Way Hill, Berke- ley. The burrows were constructed among the large basal roots of a California laurel growing on the top of the bank. The bur- row entrances were all within four to five inches of each other and were frequently hidden by roots or cracks in the ground. They were 5 mm. in diameter and penetrated the moist clay soil as a smooth circular hole for from three to six inches. Numerous cells were constructed along each burrow and were seldom more than an inch away from those in the same or adjacent series. All of the bees had emerged and several females had constructed fresh burrows, the cells of which were waxed, and provisioned with a spherical ball of pollen measuring 5 mm. in diameter. The eggs were white, slightly bowed, and 3 mm. long by less than 1 mm. wide. This species was also found nesting at the Orinda Crossroads, Contra Costa County, in February, 1940. The mature bees were unemerged and were taken from cells among the roots of a California buckeye at the top of a six foot bank. — J. W. MacSwain. 1 Linsley, E. G. 1939. New species of andrenid bees from California. Pan- Pac. Ent., 15:155-162. oct. 1945] Delong— retusanus 135 A NEW GENUS— RETUSANUS— AND FIVE NEW SPECIES OF MEXICAN LEAFHOPPERS (Homoptera, Cicadellidae) BY DWIGHT M. DeLONG Department of Zoology and Entomology, Ohio State University The members of the Genus Retusanus are characterized by being densely covered by minute brown spots. They are appar- ently Deltacephaloid in type, the elytron resembling the vena- tion of this group. There are many costal veinlets, the central anteapical cell is long, the outer anteapical cell is shorter and it is often divided into two or more cells. The vertex is flat or concave between the eyes and forms a definite margin with the front. The vertex is rather short and broadly rounded on the margin. The long ovipositor exceeding the long narrow p3^gofer indicates a definite relationship to the Aconuran group. Type of genus Retusanus punctatus DeLong. The species of this genus are very similar in coloration and appearance and can be separated by the male genital structures. The styles and pygofer spines are quite different in the different species while the aedeagus in lateral view shows some differences in certain species. Retusanus punctatus DeLong, new species A broad headed species marked with minute brown peppered spots. Length male 4 mm. Vertex broadly rounded, appearing almost parallel margined, less than two-thirds as long at middle as basal width between eyes. Color: Vertex pale with ocelli and two spots between them just above margin, brown. These four brown spots are about equidistant from eyes and from each other. Remainder of vertex sparsely marked with minute brown spots. Pronotum and scutellum brown, densely marked with minute brown spots. Anterior margin of pronotum behind eyes and basal angles of scutellum, rusty brown. Elytra pale subhyaline, veins dark brown, a few minute brown spots on clavus and basal portion. Face pale, rather evenly and densely marked with minute brown spots. Genitalia: Male aedeagus rather short, erect, apical third with a broad notch dividing it into two portions, an anterior narrow portion, blunt at apex, and a posterior broader portion with a pointed apex. Plates about twice as long as basal width, tapered 136 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 to blunt, rounded apices. Style long, rather narrow, deeply round- edly notched on outer margin just before apex, forming a slender, outwardly curved apical portion which is narrow but truncate at tip. Pygofer with a long basal spine which extends to apex of pygofer and a short black plate with several teeth arising just before apex of plate. Holotype male and paratype males collected at Iguala, Guerrero (elevation 2400 ft.), October 25, 1941, by Good and DeLong. Retusanus pulverus DeLong, new species Resembling pwnctatus in general appearance but with vertex more produced, and distinct genitalia. Length, male, 4 mm. Vertex roundedly rather broadly produced, less than two-thirds as long at middle as basal width between the eyes. Color: Vertex white, ocelli brown. A pair of proximal oblique spots just above margin at middle. The portion of the pronotum basal to the anterior margins of the eyes densely marked with minute brown spots. Pronotum and scutellum brown, densely marked with minute brown spots, a white spot on each margin of scutellum half way between base and apex. Elytra pale subhyaline with dark brown veins, claval area and central portion of cells of corium densely marked with minute brown spots. Face pale, a band just below margin unmarked, the other portions of face densely marked with minute brown spots. Genitalia: Male plates rather short, broad at base tapered to bluntly pointed apices. Adeagus short, erect, broadened on apical half, broadly notched at apex forming a blunt anterior portion and a posterior portion which is pointed on apical caudal margin. Styles long, rather narrow, broadly shallowly excavated on outer margin just before apex. The apical third is curved outwardly narrowed to apex which is pointed on outer apical margin. The pygofer has a short basal spine which is not as long as plate and a black plate with several teeth which is just at apex of plate. Holotype male and paratype males collected at Iguala, Guerrero (elevation 2400 ft. , October 25, 1944, by Good and DeLong. Retusanus luteus DeLong, new species Resembling punctatu-s in general appearance and coloration but with distinct genitalia. Length — male 5 mm., female 5.5 mm. Vertex broadly rounded, two-thirds as long at middle as basal width between the eyes. oct. 1945] DeLONG— RETUSANUS 137 PLATE I Retusanus luteus DeLong. Fig. 1. Dorsal view of head, pro- notum and scutellum. Fig. 2. Lateral view of head, pronotum and scutellum. Fig. 3. Female genitalia, ventral view. Fig. 4. Ante- rior wing showing venation. 138 PAN-PACIFIC ENTOMOLOGIST [vOL. XXI, NO. 4 Color: Vertex pale, sparsely clothed with minute brown spots, a pair of brown spots next ocelli and a pair of rather large brown spots just above margin at apex. Face pale just below margin of vertex, most of face densely marked with minute brown spots. Pronotum and scutellum densely clothed with minute brown spots. Elytra pale subhyaline, veins dark brown, clavus and cells on corium sparsely clothed with minute brown spots. Genitalia: Female last ventral segment deeply, broadly notched from lateral angles to near base, apex of notch narrow, entire margin embrowned. Pygofer long, narrow, ovipositor rather large, decidedly longer than pygofer. Male plates rather long, almost as long as pygofer and broadly rounded at apex. Aedeagus resembling that of punctatus but broader. The V-shaped notch at apex rather broad and reaching about one-third the distance to base. The anterior process formed by the notch rounded at apex, the posterior portion bears a short tooth on inner margin of blunt apex. Styles long, concavely narrowed on outer margins at two-thirds their length to form rather broad apical portions which are slightly notched on outer margin just before apex and bear a short tooth on outer margin of blunt apex. Pygofer with a basal spine reaching only about two- thirds the length of plate. The black plates with conspicuous teeth are rather large and are on the margin of pygofer at about the apices of the plates. Holotype male and paratype males collected at Iguala, Guerrero (elevation 2400 ft.), October 25, 1941. Allotype fe- male collected at Taxco, Guerrero, at K. 150 (elevation 5700 ft.), October 26, 1941. Paratype males also taken at Iguala, Guerrero, September 9, 1939. All specimens were collected by Plummer, Good and DeLong. Male paratype collected at Paso de Vaca, Guerrero, September 3, 1930, by Dr. Dampf. Retusanus apicatus DeLong, new species Resembling punctatus in general appearance and coloration but with distinct male genitalia. Length — male 4.5 mm. Vertex broadly rounded almost two-thirds as long at middle as basal width between eyes. Color: Vertex pale, ocelli brown and with two rather large proximal brown spots just above margin at apex. Entire vertex except anterior margin sparsely clothed with minute brown spots. Pronotum, scutellum and face densely marked with minute brown spots. Elytra white, subhyaline, veins dark brown, clavus sparsely marked with minute brown spots. Genitalia: Male plates not quite as long as pygofer, straight on inner margins, strongly curved on outer margins to form rather blunt apices. Aedeagus with a broad V-shaped apical notch almost oct. 1945] delong— retusanus 139 halfway to base forming an anterior tapered portion with a narrow apex, and a rather narrow posterior portion with a tooth on inner margin just before narrow rounded apex and a conspicious spine PLATE II Retusanus spp. Ventral and lateral views of apical portions of abdomen of males showing genital structures. just basad to tooth. The styles are abruptly narrowed at about two-thirds their length by being deeply concavely excavated on outer margins to form long slender outwardly curved apical portions. Pygofer with basal spines as long as pygofer and a small inconspicious black plate with several small teeth just before apex of plate. 140 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 Holotype male and paratype males collected at Iguala, Guerrero (elevation 2400 ft.), October 25, 1941, and Septem- ber 11, 1939, by Plummer, Good and Delong. Paratype males collected at San Geromimo, Guerrero, August 30, 1930 (M.F. 1787) and at Zincauro, Guerrero, September 2, 1930 (M.F. 1789) , by J. Parri. Retusanus irroratus DeLong, new species Resembling punctatus in general form and appearance but with distinct male genitalia. Length — male 4.5 mm. Vertex broadly, roundedly produced a little more than half as long at middle as basal width between the eyes. Color similar to punctatus. The face, pronotum and scutellum heavily marked with minute brown spots. Vertex with a pale spot around each brown ocellus, the remainder, including the median anterior portion densely clothed with minute brown spots. Elytra white, subhyaline, the veins dark brown, the claval and discal areas marked with many minute brown spots. Genitalia: Male plates short and broad, about twice as long as basal width, convexly rounded on outer margin to blunt, rounded apices. Aedeagus short, broad on apical half, notch at middle of apex forming a blunt anterior portion and a pointed apical portion. Style rather long, broadly and rather deeply excavated on outer margin just before apex; apical third curved outwardly, apex nar- rowed and truncate. Pygofer with a basal spine reaching beyond apex of plates and a rather long black plate with several teeth which arise just before apex of plate. Holotype male and paratype males collected at Iguala, Guerrero (elevation 2400 ft.), October 25, 1941, by Good and DeLong. A STAPHYLINID BEETLE NEW TO CALIFORNIA Ocypus ater (Grav.), a European Staphylinid beetle, long recorded from the Atlantic States and for many years from the seaboard areas of Washington and Oregon, has recently been found on the sea beaches to the west of San Francisco. In former years both Dr. Blaisdell and I collected along this beach without ever seeing it. This species has evidently followed the role taken by numer- ous Eurpoean species, first establishing itself in our Northwest, then working down the coast. — Edwin C. Van Dyke. OCT. 1945] POTTS— COENONYCHA 141 A NEW COENONYCHA FROM CALIFORNIA (Coleoptera, Scarabaeidae) BY ROBERT W. L. POTTS University of California, Berkeley Heretofore the members of this genus have been primarily associated with chaparal. The discovery of this apparently new species in an area of grass pastureland adds a new habitat to those previously known. Fragmentary biological notes are there- fore included as being of probable interest. Coenonycha pascuensis Potts, new species Medium-sized, narrow; pale testaceous with elytral suture, margin and base, pronotal margin and two lateral spots, and head slightly to considerably darker (in life with a reddish cast, lost in dried specimens) ; metathoracic wings fully developed in both sexes. Male: Head largely punctate, vertex with small, irregular largely impunctate area and front with largely clear short mesal line above suture; front with punctures often contiguous or sub- continguous in irregular short rows sometimes separated by one- third to one-half the width of a puncture, punctures less dense over vertex, again crowded over eyes; clypeus densely punctate and punctures larger, contiguous or subcontiguous; lateral margin of clypeus narrowly, slightly reflexed at base to strongly so at apex and anterior margin, only slightly less elevated at middle than at angles, not smooth on reflexed surface; clypeal suture distinct throughout, strongly, evenly arched toward base at middle, in shape of a bow; antennae 10-segmented. Pronotum widest at strongly rounded hind angles which are at about middle, margin evenly rounded behind, slightly sinuate before to the barely pro- duced, slightly acute anterior angles; surface smooth, shining, punctures very irregularly placed, thickest at or behind middle toward sides (about one puncture width between), sparse anteriorly and mesally (two to five puncture widths between), nearly absent at base, each with a short seta. Elytra with side margins sub- parallel; humeral umbones prominent; costae barely evident as partial, paired rows of punctures, fourth or outer pair most distinct; surface nearly smooth and shining, translucent, so veins and folding of wing beneath apparent; punctures irregular in size and placement, deep, but without distinct edges, larger ones each with a short seta. Venter with punctures less dense than above, small to large, metasternum longer than width of hind 142 PAN-PACIFIC ENTOMOLOGIST [yOL. XXI, NO. 4 coxal plates; foretarsi with first segment extending well beyond apical tibial claw; all tarsal claws cleft apically, outer tooth largest and longest. Length 8.5 mm., width 3.75 mm. Female : Similar to male but more robust, more rounded; clypeal margin more strongly reflexed, especially at outer angles, nearly smooth on reflexed surface; head and pronotum not so densely punctate, punctures more evenly spaced, setas much shorter above; foretarsi with first segment not extending beyond apical tooth of tibia; tarsal claws cleft subapically with inner tooth very fine. Length 9 mm., width 4.25 mm. Type material: Holotype male and allotype female taken in copulation 4-2-45, two and one-half miles west of Byron, Contra Costa County, California, in the collection of the California Academy of Sciences (Nos. 5468 and 5469) . Eight hundred and twenty-eight paratypes 1 from the same locality, one collected 3-8-45 by Ray F. Smith, eleven collected 3-19-45 by Ray F. Smith, seven hundred and ninety-six collected 4-2-45 by Ray F. Smith and the author, twenty-two collected 4-9-45 by the author, in the collections of the author, the University of California, California Academy of Sciences, and others. Those collected on the first two dates and on the last date, as well as thirty-nine of the total on 4-2-45 were taken at roots, while the remainder were taken after dark in sweeping. The relationships of the species are apparently with C. pallida and C. lurida, both of which are southern California species found on shrubs. It is closest to pallida in appearance, and keys out with it in the Cazier and McClay key. It may be separated from pallida by a -number of characters, the somewhat produced and slightly acute anterior pronotal angles and slightly sinuate margins before the hind angle, the rather inevident costae, the presence of large punctures on the venter, the different charac- ter of the clypeal margin apparently being the best. Unfortu- nately all known specimens of pallida are unavailable for com- parison at present due to war conditions. It is probable that better characters for differentiation will be found to exist when these specimens are again available. This species was discovered by Mr. Smith while searching for hibernating Diabrotica. The area where it is now known is in 1 In a Revision of the genus Coenonycha by Cazier and McClay (Amer. Mus. Novitates 1239, July 19, 1943) paratypes from the type locality are referred to as paratopotypes, a term which appears unfortunate, although the intended signifi- cance is valid. Topoparatype, while lacking the euphony of the other, seems to this author to more clearly convey the intended meaning. oct. 1945] POTTS— COENONYCHA 143 the open, grassy foothills to the east of Mount Diablo, in the range which forms the western boundary of the San Joaquin Valley. The general aspect is of pastureland. The site from which all the specimens were taken is less than an acre in extent, on a northeast exposure which varies in slope from about five to thirty per cent. The plants are primarily annuals, and a majority are not native: Er odium botrys, Avena, Hordeum murinum, Lupinus, Medicago hispida, Brodiaea capitata, and Echinocystis fabacea. A few native grasses may be present in small numbers. Trees and shrubs are absent from the area, although an occasional oak tree occurs on the same hillside. The soil type, according to Carpenter and Cosby 2 is Contra Costa sandy loam. Scarab larvae, of two sizes, were found in soil samples but have not been identi- fied as this species as yet, nor was their association with any one plant possible. The adults apparently spend the day partially or completely but not deeply buried in the soil near the roots of the various plants. Observation at the site, and soil samples brought into the laboratory and sifted confirmed the fact that specimens were most common in portions of the area where the soil was some- what moist and plants were of medium height, about 6 to 8 inches. They were less common in tall grass and manroot clumps where the soil was more moist, nor were they common in portions of the area where the soil was dryer and the plants short. In sweep- ing, the specimens appeared to be most common in areas of medium plants. Less than six per cent of the specimens taken in sweeping were females, whereas approximately fifty per cent of the speci- mens taken at roots were females. The species, so far as is known, is quite localized, not being found in similar areas to the north a distance of only a few miles. This absence from these areas is not positively proven as a night search was not possible, however, a thorough day search was completely unfruitful. It would nevertheless be the opinion of the author that further investigation will prove the species wide- spread in the sandy loam pastureland along the foothills border- ing the San Joaquin Valley. 2 Carpenter, E. J. and S. W. Cosby, 1939. Soil Survey of Contra Costa County, California, U.S.D.A. Soil Survey Series 1933 (26) :26 and map. 144 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 IXODES TOVARI, A NEW SPECIES FROM MEXICO 1 (Ixodidae) \ BY R. A. COOLEY Senior Entomolgist, TJ. S. Public Health Service Ticks received for identification on March 14, 1945, from Dr. Raul M. Tovar, Departamento de Investigaciones Medicas, Hos- pital General, Mexico D. F., Mexcio, included seven lots of an Ixodes which is new to science and is here described and figured. Accession records, all from “hares,” are as follows: 21618, Bravo, Nuevo Leon, Mexico, 19 adults, 4 nymphs, 2 larvae ; 21620, Torrecilla, Guanajuato, Mexico, 1 male, 1 female; 21621, Comontoso, Guanajuato, Mexico, 1 male, 1 female; 21623, Bravo, Neuvo Leon, Mexico, 6 males, 1 nymph; 21624, Bravo, Nuevo Leon, Mexico, 1 male; 21625, Bravo, Nuevo Leon, Mexico, 2 males, 1 nymph; 21628, Bravo, Nuevo Leon, Mexico, 1 nymph. Ixodes tovari Cooley, new species FEMALE Figures 1 and 2 Body. Length (unfed), tip of hypostome to posterior margin, 2.27; width, 1.15. 2 Oval, widest back of the middle, scutum occu- pying two-thirds the length of the body not including the capitu- lum. No fully engorged specimens available, but one specimen well advanced in feeding measures 6.5 in length and is slightly wider behind. Capitulum. Length, tip of hypostome to tips of cornua, 0.72; width of base, 0.375. Dorsal surface of basis with sides converging posteriorly. Profile lines of anterior side of basis showing a shoulder each side of the insertion of the chelicerae. Posterior margin concave, salient. Cornua about as long as wide, termi- nally rounded. Porose areas small, often difficult to see; either oval or reniform, placed far apart near the posterior side near the cornua. Palpi long, article 2 a little longer than 3. Outer profile line straight or mildly convex; inner profile line convex. Stalks of the chelicerae very long. 1 From the Rocky Mountain Laboratory (Hamilton, tute of Health. 2 All measurements in this paper are in millimeters. Mont. ) , National Insti- oct. 1945] COOLEY— IXODES TOVARI 145 Figure 1 Ixodes tovari, n. sp. A. Female capitulum and scutum, dorsum. B. Female capitulum and coxae, venter. C. Female hypostome. D. Spiracular plate. E. Female metatarsus and tarsus, leg I. F. Female metatarsus and tarsus, leg IV. G. Nymph capitulum and scutum, dorsum. H. Nymph capitulum and coxae, venter. I. Nymph hypostome. J. Nymph spiracular plate. 146 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 In ventral view, basis is mildly constricted back of the auri- culae; posterior margin very broadly rounded, salient. Trans- verse sutural line visible. Auriculae as long, thin horns directed downward and backward. Palpi with a few long and a few short hairs. Hypostome. Long, narrow, bluntly pointed. Denticles 4/4 on the distal end, then 3/3 for about three-fourths the length, then 2/2 to the base. Lateral denticles much larger than the medians. Length, 0.45. Scutum. Length from 0.99 to 1.11; width, 0.78 to 0.84. Oval, wider anterior to the middle. Lateral carinae present as moderate, nearly parallel elevations extending from the scapulae to near the postero-lateral margins, with top rounded. Cervical grooves as faint lineal depressions, first convergent, then divergent. Surface smooth, shining, Hairs few, of moderate length and each in a pit which is larger than the fine punctations. Legs. Moderate in length and size. Tarsi long, tapering. Length of tarsus I, 0.54; metatarsus, 0.27. Length of tarsus IV, 0.42; metatarsus, 0.30. Coxae. All coxae mildly convex. Internal spur long on coxa I, absent on II, III, and IV. External spurs short on all coxae and progressively smaller from I to IV. Spiracular plate. Broad oval with the longer axis transverse. Length, 0.27; width, 0.24. Genital aperture. Opposite the intervals between coxae III and IV. MALE Body. Oval, a little wider behind. Total length, tip of palps to posterior margin, 1.59 to 1.86; width, 0.84 to 1.02. Capitulum. Length, tips of palpi to tips of cornua, 0,45; great- est width of basis, 0.27. Dorsum of basis broad, mildly convex, with lateral margins converging posteriorly; surface punctate. Cornua distinct, pointed, about as wide as long. Palpi long, wide; combined length of 2 and 3, 0.30; width of palpus, 0.12. In ventral view, basis rounded and salient behind and with the short, rounded auriculae in the same plate as the posterior salience. Palpal article I with a ventral edge continuing the ven- tral edge on 2 and 3. Ventral edge of 2 with several long hairs. Other short hairs numerous on the palpi. Hypostome. Long, bluntly pointed apically. A few long lateral denticles near the middle. Ventral surface longitudinally grooved with about 17 diagonal crenulations on each half. Length, 0.30. Scutum. Evenly convex excepting the antero -lateral areas which are mildly concave. Lateral carinae absent. Cervical grooves faint or absent. Pseudoscutal areas faintly diffentiated by color or by having fewer punctations. Numerous long hairs present, each in a pit. Punctations moderate in size, deep. oct. 1945] COOLEY— IXODES TOVARI 147 Ventral plates. Median plate more than twice as long: as the anal plate. Adanals wider in front. Long:, fine hairs and large punctations numerous on the median plate. Long,, fine hairs also on anal and adanals but true punctations are absent. Legs. Essentially as in the female. Length of tarsus I, 0.42; metatarsus, 0.21. Length of tarsus IV, 0.36; metatarsus, 0.225. Figure 2 Ixodes tovari, n. sp. Male. A. Capitulum and scutum, dorsum. B. Capitulum, coxae and ventral plates, venter. C. Hypostome. D. Spiracular plate. Coxae. Essentially as in the female but internal spur on I longer. Spiracular plate. Oval, large and with the longer axis longitu- dinal. Length, 0.36; width, 0.105. Genital aperture. With its large flap between coxae III. NYMPH Capitulum. Length, tip of hypostome to tips of cornua, 0,33; greatest width of basis, 0.21. Posterior margin of basis nearly straight, salient. Lateral margins divergent posteriorly. Punc- tations and hairs absent. Cornua distinct, divergent, a little longer than the width at the base. In ventral view, basis narrower back 148 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 of the auriculae. Transverse sutural line visible. Auriculae as short, rounded retrograde spurs. Hypostome. Long and narrow, Dentition 3/3 for the apical half, then 2/2 to the base. Lateral denticles much larger than the medians. Length, 0.23. Scutum. Oval, short, widest at about the middle, broadly rounded behind. Lateral carinae faintly indicated near the antero- lateral margins. Cervical grooves as shallow, lineal, divergent depressions. Surface smooth, impunctate; hairs short, few, scat- tered. Coxae. Essentially as in the adults. Spiracular plate. Large, circular, diameter about 0.10. Holotype, female from 21621. Allotype , male from 21621. Paratypes, females, males, and nymphs from 21618, 21623, 21624, and 21625. The type materials have been deposited as follows: holotype, allotype, 21621, and some paratypes, in the Rocky Mountain Laboratory; paratypes, 2 females, 1 male, 1 nymph, 21618, U. S. National Museum, Washington, D. C. ; paratypes, 1 female 21618, 1 male 21623, 1 nymph 21623, Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts; paratypes, 1 fe- male 21618, 1 male 21625, Department of Entomology, Univer- sity of California, Berkeley, California; paratypes, 1 female 21618, 1 male 21624, Dr. Raul M. Tovar, Mexico D. F., Mexico. In a general way, this species resembles scapularis, affinis, and ozarkus, but the female of tovari is easily distinguished by its long, horn-shaped auriculae. The male of tovari has the hypostome of unique appearance which separates it from all known American species of this genus. This tick is named in honor of the collector. JAN OBENBERGER Through the courtesy of a soldier of the Fifth Army Corps, recently returned from Prague, I have been notified that my friend, Dr. Jan Obenberger, the Director of the Czecho-Slovakian National Museum and a world specialist in the family Bupresti- dae of the Order Coleoptera, is alive and well. — Edwin C. Van Dyke. oct. 1945] SCHUSTER— PHOTOPSIS 149 AN INTERESTING NEW BRACHYPTEROUS SPECIES OF PHOTOPSIS (Hymenoptera, Mutillidae) BY R. M. SCHUSTER Cornell University, Ithaca, N. Y. Brachypterous Mutillidae are not often encountered; in North America Myrmilloides grandiceps (Blake) is constantly brachy- pterous, Dasymutilla waco (Blake) occasionally brachypterous, rarely apterous, Dasymutilla hector (Blake) very rarely brachypt- erous, and Morsyma ashmeadii Fox, as far as is known, is apter- ous. These are the only previous records of brachypterous and apterous male Mutillidae from North America; therefore, the discovery of a new short-winged form is of some interest. As far as can be judged, the specimen is a fully developed, not teneral, and the wings are fully developed and hardened. Photopsis brachyptera Schuster, new species Male. Length 4.7 mm. Rufo-ferruginous, the legs and antennae considerably lighter, more yellowish ; very weakly setigerously punctured, except for the alitrunk, which is largely areolate- reticulate, the pubescence sparse, silvery, erect, pilose; wings greatly abbreviated, not reaching beyond petiole. Head, including eyes, 1.05 mm. wide (1.1 as wide as thorax in front of tegulae), rather moderately extended behind the eyes, the length behind the eyes 0.30 mm. (three-fourths the length of the eyes). Ocelli rather small, the posterior behind the supraorbital line; length of the posterior 0.12 mm.; their distance apart, 0.22 mm. (1.83 their maximum diameter) ; their distance from the front ocellus 0.13 mm. (slightly greater than the length of the posterior ocelli) ; their distance from the nearest eye-margins, 0.30 mm. (2.5 their length) ; the ocellar area more deeply pig- mented than the rest of the head. Eyes somewhat silvery, dis- tinctly facetted, 0.40 mm. long, 0.36 mm. wide. Pubescence very moderate, of long, nearly silvery pilose hairs arising from scat- tered, very small punctures (somewhat closer on the occiput) ; ex- cept for these punctures the head is smooth, polished, shining. Posterior and posterolateral angles evenly rounded into the occipi- tal region. Antennal tubercles separated from each other by the length of the posterior ocelli, evenly concave between and below them, not carinate; clypeal region only moderately developed, the distance from the anterior margin to a line drawn through the dorsal margins of the antennal tubercles one-half of the length 150 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 between the eyes on the frons; the anterior clypeal margin not reflexed, not produced, medially rather strongly, evenly convex, with scattered, long-setigerous, rather strong punctures. Mandi- bles moderate in size, evenly curved, not elbowed, apically bluntly bidentate, a smaller tooth within; ventrally very strongly incised and dentate about half way from apex to base of mandible, basal half of mandible with rather long, coarse hairs. Scape about 0.42 mm. long (as long as the first two flagellar segments), strongly curved, moderately setigerously punctured dorsally, the hairs rather coarse, moderately long, chiefly erect; pedicel over 1.5 times as long as wide, two-thirds the length of the first flagellar segment; flagellum slender, the first article twice as long as wide, the second and third subequal in length and scarcely a fourth longer than the first; entire flagellum silvery puberulent, the pedicel with longer silvery hairs. Alitrunk 0.97 mm. wide at tegulae (less than width of head) ; humeral angles absent, but the prothorax rather square in front; pronotum characteristically, coarsely but shallowly hexagonally areolate-reticulate, the ridges between the areolations thin and sharply defined; pubescence of pronotum denser than that of head, erect, pilose, argenteous. Mesonotum similarly, but very shallowly, obsoletely areolate, the lateral areas of it nearly smooth, except for sparse, long-setigerous punctures, the hairs slightly ferru- ginous-tinged ; parapsidal furrows obsolete, scarcely distinct. Scutellum similarly, but quite deeply sculptured, not at all strongly inflated, nearly on the same plane as the mesonotum and propo- deum. Mesopleura and mesosternum also areolate-reticulate, the mesosternum entirely lacking any carinae or dentate processes. Propodeum dorsally similarly reticulate, but the reticulations much larger; the lateral faces and the upper part of the posterior face similarly sculptured, but the posterior face is smooth medially and apically, except for sparse punctures that bear prominent, upward- pointing, silvery plumose hairs; the lateral and posterior faces of the propodeum are separated from each other at a sharp angle. Forewings short, scarcely reaching beyond propodeum, with the venation strongly reduced; C, R-M, CU+Cui and 1st A are present and infuscated on the basal two-thirds of the wing; the stigma is also distinct and infuscated; cell M is enclosed, and slightly longer than cell Cu+Cui, which is also distinct; cell M 3 is enclosed, except near apex; cell M 4 is entirely open on the outer side; all other cells apicad of these are entirely absent. The hind wings are even more reduced, and the infuscated stubbs of the veins are limited to the basal third of the wing. Legs lighter than the rest of the thorax, the coxae, trochanters, femora and tibia with sparse, long, erect pilose pubescence; the tarsi with dense, more or less appressed, fine silvery hairs; the serrate calcars of the hind tibiae are of the same color as the legs, the longer is three-fourths as long as the metatarsus. Abdomen sparsely punctate and pubescent; the petiole, meas- ured dorsally, wider at apex than its maximum dorsal length, its oct. 1945] SCHUSTER— PHOTOPSIS 151 basal width scarcely over a third that of the apex, gradually dilated toward the apex, which is evenly rounded into the second tergite, from which it is scarcely separated, even laterally; viewed laterally, it is very weakly convex above, not at all nodose, the anterior two-thirds are nearly plane, while the apical part is rounded into the second tergite; ventrally it is strongly separated from the second tergite; the flat dorsal plane moderately coarsely, sparsely punctate, bearing long erect, silvery hairs, Second ter- gite smooth, polished, shining, except for very few, scattered seti- gerous punctures bearing long silvery pilose hairs; the apical margin, in addition, with a few inconspicuous long-plumose hairs; pigmentation of second tergite rather deeper than that of rest of body, except ocellar region. Apical tergites similarly pubescent, also with some scattered, sparse, small plumose hairs, nearly im- punctate; the pygidium not margined laterally or apically. Felt lines of second tergite less than a third the length of the tergite, situated medially between the base and apex of the tergite; those of the second sternite similar, but much shorter, situated behind the median line of the sternite. Second sternite sparsely punctate, bearing long, simple, or shortly plumose hairs, and a band of somewhat shorter, longer-plumose hairs at apex; apical sternites similarly, but much more sparsely pubescent, except the third sternite, which also has a rather conspicuous band of plumose hairs at its apex. Holotype: Berkeley, California, October 4, 1919, in the collection of Cornell University (Type No. 2196). This species is the first known brachypterous Photopsidine wasp. At first it was felt that the specimen might conceivably be an immature specimen, in which the wings were not yet mature, but there seems to be no evidence to support such a thesis. It seems to be somewhat allied to Photopsis hyalina (Blake) and Photopsis mesillensis Ckll. The absence of processes of any kind on the mesosterna throws this species into the group Photopsis, as distinguished from the group Odontophotopsis, which was unfortunately founded on a generic basis. It differs from all known species of Photopsis by the following combination of characters: brachypterous wings, hexagonally-areolate thorax, gradually dilated petiole sessile dorsally with the second tergite and not at all nodose, and the mesally convex, poorly developed clypeal area. The rather quadrate head, with small ocelli and rather small eyes, with the head scarcely less long behind the eyes than the length of the eyes, and the strongly ventrally incised and dentate mandibles distinguish this species from P. hyalina and mesillensis; hyalina furthermore differs in that the parapsidal furrows are more distinct. 152 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 A NEW LARICOBIUS FROM OREGON (Coleoptera, Derodontidae) BY KENNETH M. FENDER McMinnville, Oregon Laricobius nigrinus Fender, new species Males, Black and shining above, antennae brunneous, legs and ventral surface piceous, pubescence piceous to ashy. Head wider than long, rather finely closely punctured. Behind the antennae and between the eyes is a rough oval of very coarse punctures. Pronotum wider than long, widest at the middle, base slightly wider at the angles than the apex, sides strongly sinuate, basal and apical angles nearly equally prominent; closely punctate and with larger coarse punctures scattered throughout. Elytra wider than thorax at the humeri, sides faintly, arcuately divergent to the apical third, then rapidly rounded to the suture; elytral striae composed of large subquadrate punctures, interstriae finely, sparsely punctate. Dorsal pubescence composed of fine erect hairs. Legs and under- surface finely punctured and with a fine ashy pubescence which is recumbent and sparse. Lateral lobes of the asdeagus obliquely truncate as in L. rubidus Lee. 1 Length 2 to 2.3 mm. Female. Piceous and with ashy pubescence, otherwise similar to the male. Length 2.5 mm. Holotype male, allotype female, and five paratypes, June 20, 1904, Bear Springs, Wapinitia cut-off, Oregon. One paratype, October 29, 1933, Creston, British Columbia, collected by G. Stace Smith. Laricobius nigrinus can be separated from the other two North American species by its color and the shape of the pronotum. The color is black to piceous in nigrinus, uniformly testaceous to dark reddish brown in L. laticollis Fall and black with a wide red median vitta on each elytron in L. rubidus Lee. In nigrinus the pronotum is widest at the middle and the basal margin is wider at the angles than is the apical margin. In both rubidus and laticollis the pronotum is widest in front of the middle and the basal margin is narrower at the hind angles than is the apical margin. The author is indebted to Mr. C. A. Frost for calling his attention to this new species. 1 Brown, W. J., 1944, Canad. Ent„ 76:8. oct. 1945] ROSS— NEMATINE SAWFLY 153 A NEW TRIBE AND GENUS OF NEMATINE SAWFLY ( Hymenoptera, Tenthredinidae) BY HERBERT H. ROSS Illinois Natural History Survey, Urbana, Illinois The following new genus, Pristola, combines many character- istics which are unlike any known genera of Nematinae. The venation of both wings is characterized by the atrophy of vein 2A & 3A, which would place the genus in the tribe Pseudodi- neurini. From this tribe the genus Pristola differs in the striking characters of the mesonotum, fig. 3. Most conspicuous of these are the semi-obliterated praescutal structures and the long, ex- posed postnotum of the mesothorax; the male and female geni- talia are also of very unusual shape. In the Pseudodineurini the praescutum is well defined, and the exposed portion of the post- notum is short and almost hidden under the large and projecting post-tergite. On the basis of these and other differences a new tribe is proposed for the reception of Pristola. Pristolini new tribe Characteristics. Venation typical of the specialized Nematinae, the front wings with both 2 r and the basal lobe of 2 A & 3A absent; general proportion of wings resembling in other respects those of Nematus. Mesopleurae with a well-defined, linear prepectal suture. Mesonotum, fig. 3, with praescutal sutures only faintly indicated, becoming obsolete some distance from meson; mesoscutellum with only a narrow post-tergite which is on a level with the postnotum. Visible portion of postnotum long and flat, so that the post-tergite and metascutellum are far apart; metascutellum arcuate. First abdominal tergite with its acrotergite also flat and long. Erected for the single genus Pristola. Pristola new genus Characteristics. Body elongate and slender. Head wide, fig. 2, somewhat short and stocky from lateral view; clypeus very shallow and extending scarcely beyond the base of the mandibles. Labrum semi-circular and of only moderate size. Antennae 9-segmented, long and filiform, the last four segments gradually diminishing in length, the apical segment four times as long as wide and pointed at tip. Mandibles with lateral aspect narrow and blade-like; with anterior aspect as in fig. 2, each mandible possessing a long curved apical tooth and a small sharp subapical tooth. Legs slender, 154 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 tarsal claw also slender and long, without any trace of a sub- apical tooth. Genotype. Pristola macnabi new species. In the key to the genera of the Nematinae (Ross 1937: p. 75) , Pristola will run to couplet 9 on the basis of the atrophy of 2A & 3A in both front and hind wings. Couplet 9 can be emended as follows to accommodate Pristola: 9. Clypeus shallow, not extending over base of mandibles, fig. 2; post-tergite very narrow, postnotum flat and exposed, fig. 3; mandibles with only a minute inner tooth Pristola Ross — . Clypeus extending as a broad shelf over the basal half of the mandibles, fig. 1 ; post-tergite large and triangular, with exposed part of the postnotum short and declivous (similar to Ross 1937, fig. 124) ; mandibles tridentate (Ross 1937, fig. 318) , the subapical teeth large and prominent 9a 9a. Ocelli forming a wide triangle (Ross 1937, fig. 294) P seudodirveura Konow — . Ocelli forming a flatter triangle (Ross 1937, fig. 295) Kerita Ross Pristola macnabi new species Male\. Length 6 mm. Body straw color, with the antennae, ocellar region, middle portion of the mesonotum, most of the ab- dominal dorsum, sutures of mesopleurae and varying lines on dorsal border of legs, dark brown to black. Wings hyaline, vena- tion dark brown. Body and appendages moderately hairy. Head shining, ocellar area prominently raised, with rounded margins; antennae very long and filiform ; mesonotum and mesopleurae highly polished with only extremely fine punctation. Wings very List of Abbreviations for Figures ap — apiceps atg — acrotergite ba — basiura bv — basivolsella cn — cenchri dv — distivolsella gc — gonocardo gl — gonolacinia gs — gonostipes h — harpes pn — postnotum pp — praeputium so — sclerora ta — tangium oct. 1945] ROBB — NEMAT1HE SAWFLY 155 Explanation of Figures Fig. 1. Kerita fidala Ross: Clypeal region of head. Figs. 2- 12. Pristola macnabi Ross: fig. 2, front of head; fig. 3, dorsum of thorax; fig. 4, apical sternite; fig. 5, eighth sternite; fig. 6, male genitalia, abossicular aspect; fig. 7, penis valve; fig. 8, volsella, dorsal aspect; fig. 9, volsella, meso-dorsal aspect; fig. 10, sheath, ventral and lateral aspect; fig. 11, lance; fig. 12, lancet. 156 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 long. Apical eighth tergite produced into a slightly convex, trun- cate process, fig. 5. Apical sternite elongate, tapering at apex, the tip fairly narrow and truncate, fig. 4. Male genitalia, fig. 6, with large, submembranous gonocardo, moderately wide gonostipes and long harpes. Parapenes declivous, moderately long, and angled laterad near apex. Volsella, fig. 8, with distivolsella short and ovate; gonolacinia with body plate- like and held at right angles to basivolsella, fig. 9, so that from the dorsal aspect, fig. 8, it appears as a thickening along the top of the volsellae. Apiceps thin and platelike, but fairly long, moderately wide, and round at apex, at its base partially fused with the distivolsella. Penis valves elongate, with a sclerotized band along the abossicular side of the valviceps, whose tip is at- tenuated into a long, slender, whiplike process. Female. Length 7 mm. Color almost entirely reddish brown with dark areas similar to those of male but much less extensive. General structure similar to male. Sheath, fig. 10, with lateral aspect blunt and rounded at apex, dorsal aspect gradually narrow- ing to a semipointed apex; cerci short. Saw extremely long and slender. Lance, fig. 11, with a long, slender radix twice as long as lamnium; lamnium divided into about eight segments, the apical one minutely serrate on its dorsal margin. Lancet, fig. 12, with ventral margin neither lobed nor toothed, but forming a sclerora which occupies half the width of the radix and gradually tapers to a narrow marginal ribbon toward the apex of the lamnium; lamnium divided into twelve irregular segments; the first six sutures do not reach the ventral margin but the apical six reach the margin and have a very small spiculella near the sclerora. Holotype, male. Boyer, Oregon, April 25, 1936 (INHS). Allotype, female. Same data but April 11. (INHS). Paratype. Oregon: Same data, April 11, 4S, 2$ ; April 18, 1 $ ; April 25, IS ; May 2, 1937, 1 5 ; May 5, 1935, 2 S, 1 $ ; May 15, 1937, 1 S ; May 22, 1937, 1 S . New Hampshire: Mt. Washington, 6000 ft., August 6, 1939, B. Arenburg, 1 S . (Mass. Agr. Coll.) . It is unusual that this species should be found in two places so far apart. This situation is reminiscent of certain species of Pristiphora, many of which have few known records but these are scattered from coast to coast. oct. 1945 ] KAPP AND SNOW — APIOCBBIDAE 157 CATALOGUE OF APIOCERIDAE OF THE WORLD BY WILLIAM F. RAPP, JR. AND WILLIS E. SNOW The family Apioceridae is composed of large flies which are restricted to arid or semi-arid regions. Very little work has been done in this family until recently when Cazier 1 revised the North American species and Hardy 2 revised the Australian species. Since the publication of the Kertesz catalogue in 1906 so many new species have been described that it has been thought advisa- ble to bring it up to date. The following is a comparison of the Kertesz catalogue and the present paper. Kertesz 1906 Apiocera 9 Apomidas 1 Megascelus — Neorhaphiomidas — Rhaphiomidas 4 Rapp & Snow 1945 35 1 2 12 14 50 Genus Apiocera Westwood aldrichi Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 193-194. alleni Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 606. augur Osten Sacken, Biol. Cen. Amer. Dipera, vol. 1, p. 212 (1887) ; Painter, Ann. Ent. Soc. Amer., vol. 25 (1932), pp. 354-355; Painter, Bui. Univ. Kans., vol. 37 (1936), p. 192. beameri Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 198-199. bilineata Painter, Ann. Ent. Soc. Amer., vol. 25 (1932), p. 351. braunsi Melander, Milwaukee Bui. Wis. Soc., vol. 5 (1907), p. 125. Arizona California California Mexico New Mexico Texas California New Mexico Cape Colony, South Africa 1 Cazier, M. 1941. Revision of North American Apioceridae. Amer. Midi. Nat., 25:589-631. 2 Hardy, G. H. 1940. Miscellaneous Notes on Australian Diptera, VII Proc. Linn. Soc. N. S. W., 65:484-493. 158 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 caloris Painter, Bui. Univ. Kans., Vol. 37 (1936), pp. 194-195. Arizona clavator Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 196-197. Mexico convergens Painter, Bui. Univ. Kans., vol. 37 (1936), p. 196. California deforma Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 52. Western Australia exta Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 609. California fuscicollis Westwood, London and Edinb. phil. Mag 1 , and Journ. of Sci., vol. 6 (1835), p. 449; brevicornis Wied., Aussereurop. zweifl. Ins., vol. 2 (1830), p. 646; asilica Westwood, Lon- don and Edinb. phil Mag. and Jour, of Sci., vol. 6 (1835), p. 449; bigotii Macq., Dipt, exot., suppl. 2, p. 49 (1847). Australia Queensland New So. Wales Victoria Tasmania haruspex Osten Sacken, Bui. U. S. Geol. Surv., vol. 3 (1877), p. 287; Painter, Ann. Ent. Soc. Amer., vol. 25 (1932), pp. 352-353; Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 191-192. Arizona Brit. Columbia California Idaho Oregon Wyoming hispida, Cazier, Amer. Midland Naturalist, vol. 25 (1941), p, 605. California immedia Hardy, Proc. Linn. Soc. N. S. W., vol. 65 (1940), p. 488. Australia New So. Wales imminwta Hardy, Proc. Linn. Soc. N. S. W., vol. 65 (1940), p. 489. Australia New So. Wales Queensland infinita Cazier, Amer. Mid. Naturalist, vol. 25 (1941), p. 613. California interrupta Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 192-193. California intonsa Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 610. Arizona California maerens Westwood, Areana Entomol., vol. 1 (48) (1841), p. 551. Australia maritima Hardy, Proc. Linn. Soc. N. S. W., vol. 58 (1933), p. 416. Australia Queensland New So. Wales oct. 1945] RAPP AND SNOW— APIOCERIDAE 159 martinorum Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 197-198. melanura Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 611. minor Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 52. newmani Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 53. norrisi Hardy, Proc. Linn. Soc. N. S. W., vol. 65 (1940), p. 489. notata Painter, Bui. Univ. Kans., Vol. 37 (1936), pp. 199-200. obscura Phil., Verh. zool. bot. Ges. Wien., vol. 15 (1865), p. 703. parkeri Cazier, Amer, Midland Naturalist, vol. 26 (1941), p. 607. pallida, Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 50. pearcei, Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 603. philippii Brethes, Rev. Chil. Hist. Nat., vol. 28 (1924), p. 104; brevicornis Phil., Verh. zool. bot. Ges. Wien., vol. 15 (1865), p. 702. pica Norris, J. Roy, Soc. W. Aust., vol. 22 (1930), p. 54. tonnoiri Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 52. trimaculata Painter, Bui. Univ. Kans., vol. 37 (1936), pp. 195-196. Genus Megascelus Philippi nigricornis (Phil.), Verh. zool. bot. Ges. Wien., vol. 15 (1865), p. 683. Genus Neorhaphiomidas Norris hardyi Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p, 64. pinguis Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 64. Idaho Oregon Arizona West Australia West Australia Australia Queensland California Chile Arizona California West Australia California Chile West Australia West Australia California Chile WestAustralia WestAustralia 160 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 Genus Rhaphiomidas Osten Sacken abdominalis Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 624. acton Coquillett, West Amer. Scientist, vol. 7 (1891), p. 84; Townsend, Proc. Cal. Acad. Sci., vol. 4 (1895), p. 602; Painter, Bui. Univ. Kans., vol. 37 (1936), p. 188. aitkeni Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 623. episcopus Osten Sacken, U. S. Geol. and Geog. Survey of the Terr., vol. 3 (1887), p. 281; Coquillett, West. Amer. Sci., vol. 7 (1891), p. 85; Townsend, Proc. Cal. Acad. Sci., vol. 4 (1895), p. 603; Painter, Bui. Univ. Kans., vol. 37 (1936), p. 188. maculatus Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 628. maehleri Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 627. mellifex Townsend, Proc. Cal. Acad. Sci., vol. 4 (1895), p. 604. painteri Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 622; xanthos Townsend, Trans. Amer. Ent. Soc., vol. 27 (1901), p. 163; xanthos Painter, Bui. Univ. Kans., vol. 37 (1935), p. 189. parkeri Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 625. terminatus Cazier, Amer. Midland Naturalist, vol. 25 (1941), p. 622; Coquillett, West. Amer. Sci., vol. 7 (1891), p. 85 (episcopus O. S.) ; Townsend, Proc. Calif. Acad. Sci., vol. 4 (1895), pp. 603-604 (mellifex Towns.) trochilus (Coquillett), Can. Ent., vol. 24 (1892), p. 315 (Apomydas) ; Norris, J. Roy, Soc. W. Aust., vol. 22 (1936), p. 50; Painter, Bui. Univ. Kans., vol. 37 (1936), p. 188. xanthos Townsend, Proc. Cal. Acad. Sci., vol. 4 (1895), p. 605; mellifex, Townsend, Proc. Cal. Acad. Sci., vol. 4 (1895), p. 604; Painter, Bui. Univ. Kans., vol. 39 (1936), p. 189. California California California Lower California California California California Lower California New Mexico California California California Mexico oct. 19A5] INDEX TO VOLUME XXI* 101 Acmaeodera clausa, 108 flavomarginata, 108 gibbula, 108 lagunae, 104 nautica, 106 opinabilis, 108 scapularis, 108 trans versa, 105 Agabus confertus, 16 erichsonii, 16 obliteratus, 16 seriatus intersectus, 16 strigulosus, 16 Agaeocera gentilis peninsu- laris, 107 Aglais califomica, 38 Aleyrodes osmaroniae, 58 Aleyrodidae, 48 Alexander, C. P., Tipulidae, 91 Amblyteles montanus, 13 American Committee on Ento- mological Nomenclature, 33 Ammoplanus, 81 Ammoplanus (Ammoplanus), 86 vanyumi Pate, 87 Ammoplanus (Ammoplanel- lus), 81 umatilla Pate, 82 xila Pate, 84 Andrena rhodotricha, 134 Aphalara vtera Van Duzee, 74 Aphididae, 119 Apiocera, 157 Apioceridae, 157 catalogue, 157 Autographa egena, 13 Badister mexicanus, 102 Baker, E. W., personal, 80 Beans, pest of, 13 Blaisdell, F. E., Cryptoglossa, 23 personal, 114 Bombus edwardsii, 37 sitkensis, 37 vosnesenskii, 37 Braconidae, 125 Buprestidae, 104 Chamberlin collection, 124 Callidium pallidum, 30, 31 sempervirens, 30, 31 Calosaturnia mendocino, 32 Camras, S., Zodion, 31 Carabidae, 101 Cardiochiles, 125 aethiops, 125 bicolor, 125, 126 longimala, 127 mexicanus, 125, 128 noctis, 129 orizabae, 125, 132 ornatus, 125, 130 thoracicus, 125, 133 * New names in bold face, s] Cephenemyia jellisoni, 120 Cerambycidae, 30 Chaetogaedia monticola, 13 China, entomology in, 35 Chrysomelidae, Oregon spp., 72 Chyphotes, 89 bicolor, 89 Cicadellidae, 135 Clench, H. K., Thaumaina, 14 Cleridae, 97 Coenonycha pascuensis, 141 Coleoptera, 10, 16, 17, 23, 63, 72, 77, 88, 97, 101, 110, 115, 118, 140, 141, 152 Colias eurytheme, 34 Conoderus laurentii, 10 Conopidae, 31 Cooley, R. A., Ixodes tovari, 144 Copodisoma truncatellum, 13 Cryptoglossa, 23 angularis, 28 bicostata, 23 granulifera, 27 laevis, 26 laevis subsimilis, 27 mexicana, 29 verrucosa, 24 verrucosa carinulatus, 25 Curculionidae, 17, 118 Cuterebridae, 120 Cymatodera ovipennis, 91 Dactylolabis imitata, 91 DeLong, D. M., Retusanus, 135 Derodontidae, 152 Diptera, 11, 31, 41, 48, 91, 120, 157 mouth parts, 41 Duncan, C. D., Gordian hair- worms, 34 Dytiscidae, 16 Elateridae, 10 Entomology, professional train- ing in, 1 in China, 35 Ephialtes sanguinipes, 13 Essig, E. O., Hyalopteroides, 119 Fender, K. M., Chrysomelidae, 72 Podabrus, 77 Laricobius, 152 Ferris, G. F., Polyctenidae, 101 Goldschmidt, R. B., Mouth parts in Diptera, 41 Hare, J. E. Lipoptena depressa, 48 Hemiptera, 121 Herman, C. M., Cephenemyia, 120 Hesperobaenus feneysi, 102 Hesperoctenes eumops, 122 fumarius, 122 Dnyms in italic. 162 PAN-PACIFIC ENTOMOLOGIST [VOL. XXI, NO. 4 Hesperoctenes ( Cont. ) limai, 123 parvulus, 123 Heteropsylla mera, 74 texana, 74 Hippoboscidae, 48 Homoptera, 58, 74, 119, 135 Hornia boharti, 88 Hyalopteroides pallida, 119 Hylus arizonicus, 103 Hymenoptera, 81, 89, 125, 134, 149, 153 Hypera punctata, 118 Intracellular organisms, 39 Ixodes tovari, 144 Ixodidae, 144 Jensen, D. D., Heteropsylla, 74 Keen, F. P., forest insects, 39 Kerita, 154 Lange, W. H., Autographa, 13 Laricobius nigrinus, 152 Leech, H. B., Agabus, 16 Lepidoptera, 13, 14, 32, 109 Limnophila gruiformis, 93 sciara, 92 snoqualmiensis, 94 Linsley, E. G., Bombus spp., 37 Hornia boharti, 88 Migration of Vanessa, 109 Notes on Pleocoma, 110 Lipoptena depressa, 48 Lycaenidae, 14 MacSwain, J. W., Hornia, 88 Cymatodera ovipennis, 97 Andrena rhodotricha, 134 Mao, Ying-Tou, Cardiochiles, 125 Mastopsenius, 64 australis, 65 Megascelus, 159 Megaxenistusa, 66 rhinotermitis, 68 Melasidae, 103 Meloidae, 88 Michelbacher, A. E., Hypera, abundance of, 118 Migration, Vanessa cardui, 109 Monotomidae, 102 Mouth parts, Diptera, 41 Mutillidae, 89, 149 Neodipriqn sp., 39 Neohermes nigrinus, 37 Neolipoptena ferrisi, 49 Neorhaphiomidas, 159 Nomenclature, American Com- mittee, 33 American Commission, 33 Obenberger, J., personal, 148 Occemyia loraria, 31 Ocypus, ater, 140 Opsimus quadrilineatus, 30, 31 Orochlesis, 17 picticollis, 19 Pacific Coast Entomological So- ciety, Proceedings, 34 Papilio philenor hirsuta, 33 Paratyndaris albofasciata, 109 olneya, 109 schaefferi, 109 Pate, V. S. L., Ammoplanus, 81 Paurocephala mera, 74 Perionia variana, 39 Phalaenidae, 13 Photopsis brachyptera, 149 Phymatodes nitidus, 30, 31 Platysamia gloveri, 33 Pleocoma australis, 111 badia, 112 behrensi, 112 dubitalis, 113 fimbriata, 112 hirticollis vandykei, 112, 115 rickseckeri, 112 spp., 113, 114 tularensis, 112 venturae, 110 Podabrus bolter i, 79 cascadensis, 77 cavicollis, 80 comes, 77 conspiratus, 77 danielsi, 80 extremus, 79 extricatus, 79 falli, 77 fissilis, 79 fulvus, 78 instabilis, 80 lanei, 78 latimanus, 77 macer, 79 piniphilus, 79 pruinosus, 77 scaber, 79 Polyctenidae, 121 Potts, R. W. L., Pleocoma, 115 Coenonycha, 141 Pristolini, 153 Pristola, 153 macnabi, 154 Pseudodineura, 154 Pseudohazis eglanterina, 32 Psyllidae, 74 Rapp, W. F., Apioceridae, 157 Reinhard, H. J., new muscoid parasite, 11 Retusanus, 135 apicatus, 138 irroratus, 140 luteus, 136 pulverus, 136 punctatus, 135 Rhaphiomidas, 160 oct. 1945] 163 Ross, H. H., Nematine sawfly, 153 Sampson, W. W., Aleyrodidae, 58 Sarcophaga thyceae, 11 Saturniidae, 32 Scarabaeidae, 110, 115, 141 Schuster, R. M., Chyphotes, 89 Photopsis, 149 Seevers, C. H., Trichop seniinae, 63 Semanotus ligneus sequoiae, 30, 31 Shannonomyia albomanicata, 96 Sicus brevirostris, 31 Smith, R. F., Migration of Aglais, 38 migration of Vanessa, 109 habits of Pleocoma, 115 abundance of Hypera, 118 Snow, W. E., Apioceridae, 157 Species concept, 37 Sphecidae, 81 Staphylinidae, 10, 63, 140 Staphylinus olens, 10 Stewart, M. A., Professional training in Entomology, 1 Temnochila virescens, 30 Tenebrionidae, 23 Tenthredinidae, 153 Tetralicia ceanothi, 59 sierrae, 60 termite nests, staphylinids from, 63 Thaumaina, 14 uranothauma deliciosa, 14 Thyce sanfordi, 13 Tilden, J. W., cerambycids, 30 Saturniidae, 32 Tipulidae, 91 Trechus humboldti, 101 Trialeurodes calif orniensis, 61 drewsi, 62 Trichopsenius, 68 depressus, 69 frosti, 70 longipes, 71 xenoflavipes, 70 Usinger, R. L., Polyctenidae, 101 Van Dyke, E. C., recently es- tablished Coleoptera, 10 Bombus vosnesenskii, 37 new Coleoptera, 101 Jan Obenberger, 148 Chamberlin collection, 124 Vanessa cardui, migration, 109 Vermelio, 38 Wind, R. G., Thaumaina, 14 Xysma ceanothi, 88 Zimmerman, E. C., Orochlesis, 17 Zodion bimacula, 31 brevirostris, 31 reclusum, 31 THE Pan -Pacific Entomologist Published by the Pacific Coast Entomological Society in co-operation with The California Academy of Sciences VOLUME TWENTY-ONE 1945 EDITORIAL BOARD E. G. LINSLEY, Editor E. C. VAN DYKE, Associate Editor R. W. L. POTTS, Assistant Editor G. F. FERRIS, E. S. ROSS, R. L. USINGER R. C. MILLER, Treasurer PUBLICATION COMMITTEE E. O. Essig, Chairman 1945 M. A. Stewart F. E. Blaiadell 1946 C. D. Duncan H. H. Keifer 1947 G. F. Ferris E. O. Essig San Francisco, California 1945 11 CONTENTS FOR VOLUME XXI Alexander, C. P. Undescribed species of Tipulidae from the western United States. Part II 91 Anonymous American Committee on Entomological Nomenclature 33 Edward W. Baker 80 Frank E. Blaisdell, Sr 114 Blaisdell, F. E. Synoptic review of the known species of Cryptoglossa Solier, with description of a new subspecies 23 Camras, S. Further notes on some species of Zodion 31 Cooley, R. A. Ixodes tovari, a new species from Mexico 144 DeLong, D. W. A new genus — Retusanus — and five new species of Mexi- can leafhoppers 135 Essig, E. 0. Hyalopteroides pallida Theobald, an aphid new to North America 119 Fender, K. M. Oregon Chrysomelidae 72 Notes on the species of Podabrus of Oregon and Washing- ton 77 A new Laricobius from Oregon '.... 152 Ferris, G. F. and R. L. Usinger Notes and descriptions of American Polyctenidae 121 Goldschmidt, R. B. Evolution of mouthparts in Diptera. A counter critique.... 41 Hare, J. E. Flying stage of the deer lousefly, Lipoptena depressa (Say), in California 48 Herman, C. M. Cephenemyia jellisoni Townsend reared from nasal bot of blacktailed deer 120 Jensen, D. D. Notes on the synonymy, nymphs and distribution of Heter- opsylla texana Crawford 74 Ill Lange, W. H. Jr. Autographa egena (Guen.) a periodic pest of beans in California. 13 Leech, H. B. On three species of Agabus recorded from the state of Montana 16 Linsley, E. G. Further notes on some species of Pleocoma 110 Linsley, E. G. and J. W. MacSwain Longevity of fifth instar larvae of Hornia boharti Linsley 88 Mao, Ying-Tou Synopsis of the Mexican species of Cardiochiles Nees... 125 MacSwain, J. W. Notes on the habits of the predator Cymatodera ovipennis Say with a description of the pupa 97 Nesting habits of Andrena rhodotricha Linsley 134 Pacific Coast Entomological Society Proceedings for 1944 34 Pate, V. S. L. Notes on Ammoplanus 81 Potts, R. W. L. A new Coenonycha from California 141 Rapp, W. F. and W. E. Snow Catalogue of the Apioceridae of the world 157 Reinhard, H. J. A new muscoid parasite reared from beetles in California 11 Ross, H. H. A new tribe and genus of nematine sawfly 153 Sampson, W. W. Five new species of Aleyrodidae from California 58 Schuster, R. M. A new species of Chyphotes from California 89 An interesting new brachypterous species of Photopsis.... 149 Seevers, C. New genera and species of Trichopseniinae from Ameri- can and Australian termite nests 63 Smith, R. F. and E. G. Linsley Migration of Vanessa cardui (Linn.) 109 Smith, R. F. and A. E. Michelbacher Abundance of Hypera punctata (Fabr.) in 1945 118 IV Smith, R. F. and R. W. L. Potts Biological notes on Pleocoma hirticollis vandykei Linsley 115 Stewart, M. A. Professional training in Entomology 1 Tilden, J. W. Notes on redwood cerambycids. 30 Notes on some moths of the Family Saturniidae 32 Van Dyke, E. C. Two Coleoptera recently established in California 10 New species of North American Coleoptera 101 The Chamberlin collection of Buprestidae 124 A staphylinid beetle new to California 140 Jan Obenberger 148 Wind, R. W. and H. K. Clench Notes on the genus Thaumaina 14 Zimmerman, E. C. A new Javanese Orochlesis and a checklist of the genus.... 17 MAILING DATES FOR VOLUME XXI No. 1. February 23, 1945. No. 2. April 30, 1945. No. 3. July 30, 1945. No. 4. November 26, 1945. # ; REVISTA DE ENTOMOLOGIA An International Review of Entomology An illustrated magazine published four times a year by THOMAZ BORGMEIER, O.F.M., devoted to entomology, mainly of the neo- tropical fauna. The volumes already published since 1931 comprise thousands of pages and contain articles by leading entomologists such as F. W. Edwards, W. Horn, E. Lindner, J. W. S. Macfie, E. Martini, A. da Costa Lima, F. Silvestri, C. Menozzi, A. Reichensperger, F. Santschi, J. D. Hood, etc., with a bibliography of the current literature (economic and non-economic) of the neotropical fauna. Annual subscription $4.00 U. S. ($5.00 U. S. through booksellers). All payments are in advance. The back volumes are still on sale; price of each volume 4 U. 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