ee aad = ; Ee ea eT ieee — SS SS ee = Soe Se RES ROSES IOS : : Te LEE : ~ = a hn eg ee Ms = . bs , = Se CA aes = = Sore = . : es 7 : — ————— - — —— 7 ~ x Sa a - = : PReS > ae - aes * eee a . ~~ z = 2 : ‘ ———* accel ’ : be ase ~ ¥ - - > 3 w - ~ ‘ ~ ~ by = cox “~~ Sa ied ~ * aw sents —o= = : en SY : pea, aaa ert pa cas SE SEES a ere ToS SE ae Sooo —— Ot at pen Pe en Saye, pK pike Sire se RASA GRAS ; rs > eae “ on.) ie f : ye PROCEEDINGS OF THE ACADEMY OF NATURAL SCIENCES OF PHILADELPHIA. 1898. COMMITTEE ON PUBLICATION: Tuomas MEEHAN, CHARLES E, Smirn, Epwarp J. Nouan, M. D., Henry SKINNER, M. D., Henry A. PItspry. Epiror: EDWARD. J. NOLAN, M. D. 0 4 MS “nA \- - ) ey Vv PHILADELPHIA: ACADEMY OF NATURAL SCIENCES, LOGAN SQUARE. 1899. ACADEMY OF NATURAL SCIENCES OF PHILADELPHIA, January 31, 1899. I hereby certify that printed copies of the ProceEp1ncs for 1898 have been presented to the meetings of the Academy and mailed as follows :— Pages 9 to 152 mailed April 5, 1898, presented April 5, 1898. “* 153 to 200 ‘* May 3, 1898, . May 3, 1898. “« 201 to 248 4=‘* June 13, 1898, i June 14, 1898. “¢ 249t0328 “ July 12, 1898, sé July 12, 1898. ‘¢ 329to344 “ August 2, 1898, ts August 2, 1898. © 345 to 360 ‘ October 4, 1898, es October 4, 1898. *« 361 to424 ‘* October 15, 1898, October 18, 1898. *« 425to456 “ October 29, 1898, A November 1, 1898. ** 457 to 472 ‘* December 12, 1898, « —. December 13, 1898. ‘“* 473to488 ‘* January 13, 1899, a January 17, 1899. “© 489to504 ‘* January 26, 1899, A: January 31, 1899. EDWARD J. NOLAN, Recording Secretary. DOCKER-FOSTER CO., PRINTERS, PHILA. LIST OF CONTRIBUTORS. With reference to the several articles contributed by each. For Verbal Se at Announcements, etc., see General Index. BaxBeER, C. M. and T. D. ie CocKERELL: A new Wessel. from New Mexico : Boyer, CHARLES S. New Species of Diatoms (Plate XXIV) CaLveERT, Puitie P. Odonata (Dragonflies) from the Indian Ocean, and from Kashmir, collected by Dr. W. L, Abbott E CocKERELL, T. D. A. New and little-known Bees from Wash- ington State ‘ ConkLin, Epwin G., Pu. D. Environmental nae Sexual Dimorphism in Crepidula (Plate XXI, XXII, XXITL) Corr, Francis R. The Summer Birds of Susequehanna County, Pennsylvania Coves, Dr. Extiorr. Notes on Mr. Thomas Meehan’ s Paper on the Plants of Lewis and Clark’s Expedition across the Continent, 1804506 Dati, WittiAM H. Synopsis of the Recent and Tertiz ary Psammobiide of North America F . On the Genus Halia of Risso : Fox, Witi1am J. Contributions to a Knowledge of the eee of Brazil, No. 4—Thynninzw ‘and addi- tions . Contributions to a Knowledge of the Hy menoptera of Brazil, No. 5.—Vespide HAMILTON, S.Harsert. The Occurrence of Marcasite in the Raritan Formation HARSHBERGER, JouHn W., M.D. Botanical ‘Observations on the Mexican Flora, especially on the Flora of the Valley of Mexico . Hoveu, Garry DE N., ‘M.D. The Muscide collected by Dr. A. Donaldson Smith in Somaliland GotpsmitH, Epwarp. Volcanic Rocks of Mesozoic Age i in Pennsylvania (Plates II, I1I, IV, V) The Petrifaction of Fossil Bones . Von Ineninc, H. Contributions to the Herpetology of Sao Paulo, Brazil.—I JOHNSON, Cras. W. Diptera collected by Dr. A. Donaldson Smith in Somalil: and, Eastern Africa . New Cretaceous Fossils from an Artesian Well- -boring at Mount Laurel, N. J. ‘ JoRDAN, Davip Starr and JAmMEs ALEXANDER GuNN, JR. List of Fishes collected at the Canary Islands by Mr. O. F. Cook, with descriptions of four new Species Keer, Ina A. The Growth of Viburnum lantanoides Miehx. (Plate XXV) NETO TT) Description of a new Tethys (Aply sia) (Plate MEEHAN, Tomas. The Plants of Lewis and Clark’s Expedi- tion across the Continent, 1804-1806 . , Merriam, C. Harr. Descriptions of three new Rodents from the Olympic Mountains, Washington Mitter, GerritsS., Jr. List of Bats collected by Dr. W. i Abbott in Siam . : Descriptions of five new Phyllostome Bats A new Chipmunk from Northeastern China Notes on the Arctic Red-backed Mice ; Description of a new Genus and Species of Microtine Rodent from Siberia . Moors, J. Percy. Hyalodendron navalium, a new Genus and Species of Euplectellid Sponge (Plates XIX, XX) PALMER, T. CHALKLEY, Observations on Errant Frustules of Eunotia major (Plates VI, VII) . Pirsspry, H. A. Chitons collected by Dr. Harold Heath at Pacific Grove, near Monterey, California : A new Land Shell from Clarion Island New Species of Odontostomus from Brazil aud Argentina. Margarita Sharpii, a new Alaskan Gastropod 4 PILSBRY, H. A. and E.G. Vanarra. Anatomical Notes on certain West American Helices (Plate I) Revision of the North American Slugs: Binneya, Hem- phillia, Hesperarion, Prophysaon and Anadenulus. (Plate [X, X, XT-XIT, XU XIV, XV, AVI). : Materials toward a Natural Classification of the Cylin- drelloid Snails (Plates X VII, X VIII) , Some Cuban Species of Cerion : Ruoaps, SamueL N. A small Collection of Mammals from North Eastern China ; ’ A new Grasshopper Mouse from New Mexico. : Notes on the Fossil Walrus of Eastern North America . Seaver, Atyry. Notes on Alaskan Water Birds . SHurELDT, R. W., M. D. Observations on the Classification of Birds. Van DeENBURGH, Joun. The Gherrhonotus of the San Lucan Fauna, Lower California, with Diagnosis of other West American Species Birds observed in Central California in the Summer of 1893 . Woorman, Lewis and Guartes 8.Boyer. Fossil Mollusks and Diatoms from the Dismal Swamp, Virginia and North Carolina; Indication of the Geological Age of the Deposit. With Notes on the Diatoms . 339 482 193 12 352 316 326 348 358 368 430 110 287 354 471 486 67 219 264 475 120 194 196 126 489 63 206 414 PROCEEDINGS OF THE ACADEMY OF NATURAL SCIENCES OF PHILADELPHIA. 1898. JANUARY 4. Mr. Cuar_es Morris in the Chair. Twenty-five persons present. Papers under the following titles were presented for publication :-— “Contributions to a Knowledge of the Hymenoptera of Brazil, No. 4, Thynninae and additions,” by William J. Fox. “ The Summer Birds of Susquehanna Co., Penna.,” by Francis R. Cope, Jr. The Council reported that the following Standing Committees had been appointed to serve during the ensuing year :— On Liprary.—Charles P. Perot, Arthur Erwin Brown, Thomas A. Robinson, Henry C. Chapman, M. D., Dr. C. Newlin Peirce. Ow Pustications.—Thomas Meehan, Charles E. Smith, Henry “1 A. Pilsbry, Henry Skinner, M. D., Edward J. Nolan, M. D, 2 10 PROCEEDINGS OF THE ACADEMY OF [1898, Ow Instruction AND Lecrurrs.—Uselma C. Smith, Benjamin “Smith Lyman, Samuel G. Dixon, M. D., Philip P Calvert and Samuel N. Rhoads. STANDING COMMITTEE OF CouNCIL oN By-Laws.—Isaac J. Wistar, Theodore D. Rand, Arthur Erwin Brown, Benjamin Sharp, M. D. The Birdsboro Trap Quarries.—Mr. Turopore D. RAnp re- marked that the increasing demand for good roads has caused search to be made for the best material conveniently available. Not long ago Mr. John T. Dyer who has long wrought the extensive lime- stone quarries near Howellville, Chester Co., undertook the quarry- ing of trap rock on Hay Creek, a little over a mile southwest of Birdsboro, near Reading, Pa. The trap, probably a diabase, has come up through the Red Rocks, forming high hills on both sides of the creek, the valley of which has enabled the Wilmington and Northern R. R. to descend into the Schuylkill Valley. The re- markable feature of this trap is the evidence of intense dynamic ac- tion more recent than the rock itself. There are three quarries, two on the right and one on the left bank of the creek. The lower quarries show breasts of about a hundred feet in height, increasing as the quarrying proceeds further into the steep and high hills. Everywhere, except some portions of the upper quarry, the rock is very full of joints, the major striking N. 65° E., the others seemingly in almost every direction, as if the rock had been crushed by a very sudden pressure. The joints show, usually, slickensides on their surfaces, but there is strong cohesion through the joints, but much less than through the rock itself. These joints, of course, greatly facilitate the quarrying and crushing, though sometimes in- terfering with the drilling. At the upper quarry some rock was seen much resembling that of French Creek, and capable, like it, of being quarried in large and regular masses. in this quarry, also, were found some specimens of heulandite and probably laumontite, giving promise of fine specimens. The present output of the quarries is eleven hundred tons of crushed stone per day. The consumption of this large amount shows the remarkable increase in the use of this material. A striking feature was the cleanliness of these quarries. The blasting is done usually twice a day, but after each blast some of the quarrymen are detailed to fork up the fragments, so that the horses and carts travel over a smooth and level surface. The horses were of a quality rarely seen in quarry work, and evidently were well cared for and well treated, while the men worked industriously, without the vigorous language too often heard in quarrying opera- tions. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 11 JANUARY 11. The President, SamuEL G. Drxon, M. D., in the Chair. Twenty-seven persons present. Papers under the following titles were presented for publication :— “Proceedings of a Meeting held in Commemoration of Doctor Harrison Allen and Doctor George Henry Horn.”? “Fossil Mollusks and Diatoms beneath the Dismal Swamp, Virginia and North Carolina,” by Louis Woolman, with Notes on the Diatoms, by Charles S. Boyer. JANUARY 18. The President, Samuet G. Dixon, M. D., in the Chair. One hundred and thirty-five persons present. The deaths of Crawford Arnold and John K. Valentine, mem- bers, were announced. Dr. Persifor Frazer made a communication, illustrated with lantern slides, on “Glimpses of Russia in Europe, Asia, and Asia Minor.” (No abstract. See Proceedings, 1897, p. 405.) JANUARY 25. CHARLES ScHAEFFER, M. D., in the Chair. ‘Fourteen persons present. Papers under the following titles were presented for publication :— “On a small Collection of Mammals from Northeastern China,” by Samuel N. Rhoads. “Notes on Alaskan Water Birds,” by Alvin Seale. Israel W. Morris, Charles G. Sower, D. M. Castle and Caroline A. Burgin were elected members. The following was ordered to be printed :— ———_ — ——_— — — ' Ordered to be printed in the Proceedings for 1897. See page 505 et seq.. 12 PROCEEDINGS OF THE ACADEMY OF [1898. THE PLANTS OF LEWIS AND CLARK’S EXPEDITION ACROSS THE CON- TINENT, 1804-1806. BY THOMAS MEEHAN, The expedition of Captains Merewether Lewis and William Clark, from what was then the village of St. Louis, to the sources of the Mississippi and across to the Pacific Coast, was one of the marvels in the early history of the American Republic. The inte- rior of the continent was utterly unknown. That it was surely in- habited by wild races of men, and that wild beasts roamed through its trackless forests, comprised almost all that could be told about it. shaped marking below, near the tip of the third longitudinal vein as shown in Fig. 3. Two specimens, near Lake Abaya, May 9, 1895. OSCINIDA. Elachiptera femorata n. sp. Length 3mm. Head brownish, lower portion of the face and front more or less yellowish, orbits in certain lights are silvery, the ocellar triangle shining, the lower portion greatly attenuate and almost reaching the base of the antenne, under side of the antennze red, upper side and sete dark brown. Thorax brown, with three black stripes and covered with a grayish pubescence, which also forms a short prominent line in the center of the anterior portion of the black dorsal stripe, pleurse brownish, scutellum blackish. Abdomen black, with a narrow yellowish-white posterior margin to all the segments, venter brownish. Femora and tibie reddish, tarsi yellow, posterior femora somewhat thickened. Wings hyaline, veins dark-brown. Three specimens, Ginea, November 14th, and Sheikh Mahomed, October 11, 1894. Chlorops sp. One specimen, Sheikh Husein, October 3, 1894. HIPPOBOSCID. Hippobosca camelina (Savg.) Leach. Lipposca camelina Savigny mss. Leach, Eprob. Ins., Wern. Mem., II, 556. Tab. XXVII, figs. 11-14, 1817; Rondani, Ann. Mus. Civ. Storia Nat. Gen- ova, XII, 165, 1878. One specimen, Berbera, July 5, 1894. Ornithomyia nigricans Leach. Ornithomyia nigricans Leach. Eprob. Ins. Wern. Mem., II, 10. Tab. XXVII, figs. 7-10, 1817; Wied. Auss. Zw., 11, 609, 3; v. d. Wulp, Dipt. Sum. Exp. 57,1; v Réder, Entom. Nachr., XIX, 236, 29. Two specimens, Dada, November 21, 1894. These specimens agree with the description. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 165 THE MUSCIDZ COLLECTED BY DR. A. DONALDSON SMITH IN SOMALI LAND. BY GARRY DE N. HOUGH, M. D. One cannot offer for publication « paper on Muscide in which species are described as new without a certain amount of misgiving. So many descriptions of Muscids have been published that I fear I may have overlooked some, and that I may have added to the already too long list of synonyms. I can only say that I have con- scientiously tried to avoid this. My descriptions are Jong, but the resemblances between the Muscide are so close, that it is essential to describe new species at length if they are ever to be recognized by subsequent students. If any of the species described as new are already known, I shall be very glad to be informed of it and to publish the synonymy. Considerable space has been given to the bristles of the head, and, as I have felt obliged to introduce some new names, my de- scriptions must be prefaced by a few remarks on these bristles. Bristles of the Head.—The central feature of the muscid face is the frontal suture, which, taken as a whole, has the shape of an in- verted U,the arms making with one another more or less of an angle. If we draw a line across the face tangent to the convexity of this suture, then the part of the face dorsad of this line and between the eyes is the front. The front is distinetly divided into three parts, a median (the frontal vitta), and two lateral (the geno vertical plates). The boundary lines between the vitta and the geno-verti- cal plates are marked by rows of bristles (usually one row on each side of the vitta), which are inserted in a dorso-ventral line from a point on a level with the anterior ocellus to the ventral border of the front. These are the frontal bristles. They are in two groups which I call the ascending frontal and the trans-frontal. The ascending frontal, from one to four in number, are the most dorsad of the frontal bristles. If more than one is present, the most dor- sad is the largest, and each succeeding one is smaller (usually much smaller) than its dorsal neighbor. They are curved dorsad, caudad and more or less laterad, and are parallel to one another. 166 PROCEEDINGS OF THE ACADEMY OF [1898. The trans-frontal vary in number in different species, in the two sexes of the same species and even in different individuals of the same sex. In the female they are directed mesad and cephalad across the frontal vitta and more or less of them may decussate with their fellows of the opposite side. In the male they are generally more numerous than in the corresponding female, and they are directed cephalad with (usually) a curve dorsad or ventrad. As in the female they may decussate, but as a rule they do not. Each geno-vertical plate is continued over the vertex to the occi- pital surface in the form of a little ridge. This ridge is bounded laterad by a suture which begins at the dorso-mesal angle of the eye, runs to the vertex, over the vertex to the occipital surface of the head, and then in a ventro-mesal direction as far as the great cen- tral foramen. About half way between the vertex and the great foramen the little ridge bifurcates. The lateral branch continues in about the same direction as the main ridge, while the mesal branch runs more or less directly mesad and joins its fellow of the opposite side; thus by these two little ridges and their mesal branches a tri- angular area is marked out at the dorso-central part of the occiput. At the very beginning of each of these little ridges just mentioned, right on the vertex, stands a bristle which is called the inner verti- cal, and down a little way on each ridge just before it bifurcates stands another which I propose to call the occipito-central. Both of these bristles are present in every species that I have so far had the opportunity of examining. They vary in size in different spe- cies and in the two sexes of the same species. The inner vertical project dorsad with more or less of a curve caudad and mesad, so that they sometimes decussate a little and are almost always con- vergent. The amount of convergence varies even in individuals of the same species and sex. The occipito-central project dorsad and mesad sometimes with a curve, sometimes without a curve, some- times decussating a little with one another, sometimes apparently decussating with a bristle called the post-vertical, which will be de- scribed later. On the vertex, just laterad the beginning of the little ridge and the inner vertical bristle, stands a bristle which is called the outer vertical. This bristle varies much in size in different species and in the two sexes of the samespecies. Itis larger in the female than in the male, and is absent in the males of some species although pres- ent in their females. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 167 A little caudad, ventrad and laterad of the outer vertical, on the occipital surface of the head, there is sometimes a small bristle which curves dorsad, mesad and a trifle cephalad, apparently decus- sating with the outer vertical. I call this the occipito-lateral. Parallel to and at a variable distance caudad from the occipital margin of the eye, is a row of bristles called the cilia of the posterior orbit. They begin dorsad very near the outer vertical bristle but distinctly caudad of it and also very near but cephalad of the occi- pito-lateral. The members of the dorsal part of this row are com- monly larger and more perfectly aligned than the members of the members of the ventral portion, and there is much difference in their size and correctness of alignment in different species as well as in the distance to which they can be traced ventrad as a distinct row. Frequently there are one or more rows of exceedingly small bristles intercalated between the cilia of the posterior orbit and the occi- pital margin of the eye. The posterior orbit is the space between the cilia of the posterior orbit and the occipital margin of the eye ; it is usually narrower in the male than in the female, and may be absent. I spoke above of a triangular area marked out at the dorso-cen- tral part of the occipital surface of the head by the two little ridges and their mesal branches. This triangle and the more or less dis- tinct eminence on which the ocelli are situated, are continuous with one another over the vertex and form a differentiated portion which is occupied by a group of bristles which may be called the ocellar group. Among them we must distinguish the greater ocellar (ocel- lar pair of Baron Osten-Sacken), and the lesser ocellar. The greater ocellar is a pair of bristles usually easily distinguish- able by their larger size, which are inserted between the anterior - and posterior ocelli. They vary in size, direction and curvature in different species and in the two sexes of the same species, and in different individuals (especially males) of the same species. They are generally parallel to the lesser ocellar bristles and sometimes differ from the latter in size by a very small amount. The lesser ocellar are more numerous, from three to twelve pairs, and are usually inserted in two parallel lines (sometimes in four) which begin very close to the insertion of the greater ocellar and extend caudad a variable distance, sometimes about half way to an imaginary line joining the insertions of the inner vertical bristles, sometimes beyond this line to the occipital surface of the head. 168 PROCEEDINGS OF THE ACADEMY OF [1898. Usually the most caudal pair of lesser ocellar is somewhat larger than the rest, sometimes much larger, and it has received the spe- cial name post-vertical pair. When it is much larger and at the same time is separated by quite a space from the next pair (as im the females of Myospila, Muscina and Graphomyia) the post-verti- cal really seem to be an independent pair of bristles, but when (as. in Musca and Morellia) they are hardly distinguishable in size, are as near the next pair as that pair is to the next in the series, and still more when we find similar bristles even caudad of the post- verticals themselves it is clear that they belong to the lesser ocellar series. In some species we can see, in the middle of the frontal vitta, a more or less distinctly differentiated dorso-ventral stripe. The ven- tral end of this stripe is not much above the ventral end of the frontal vitta itself. Dorsad it broadens out and then divides inte two branches, one of which passes on each side of the ocellar emi- nence to the vertex. Inserted on the vitta some little distance below the anterior ocellus and close to this stripe (over which they decussate) we find in some species a pair of rather small bristles which I call the preocellar. Bristles which are inserted on the geno-vertical plate are called orbital. On each side of the face at the ventral end of the arm of the frontal suture, begins what is called the transverse impression of the face. This is at first a rather broad shallow depression. It passes almost horizontally laterad (becoming narrower as it proceeds) ven- trad of the eye, and can be readily traced as far as the ventro-cau- dal angle of the eye where it usually seems to end. Sometimes, however, it can be seen to be continuous with a suture of the oeci- put which runs from the latero-ventral angle of the great foramen toward and sometimes to the ventro-caudal angle of the eye. That part of the side of the face which is dorsad the transverse impression, laterad of the arm of the frontal suture and mesad of the eye is called by the German authors the wange. For this, I suggest the word gena, for reasons which will appear later. The gena is continuous dorsad with the geno-vertical plate. Ventrad of the transverse impression and ventrad of the eye, ex- tending ventrad to the edge of the mouth opening, cephalad to the — vibrissal ridge, and continuing caudad on the occiput to the great foramen, is the part which the German authors call the Backe- For this I suggest the word bucca. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 169 In English we have but one word “ cheek” for the two German words Wange aud Backe. The Wange is dorsad of the Backe, In Latin the word “ gena”’ refers rather to the upper part of the cheek, the word “bucca” to the lower part. For these reasons and be- cause the words bucca and Backe are so nearly alike, it has seemed to me wise to translate Wange by gena and Backe by bucca. The bucca is sometimes clearly defined, cephalad, from the vibrissal ridge by a distinct steep edge (I have never been able to see a suture here), at other times it is not so defined and the line of sepa- ration is an imaginary one, more or less clearly indicated by dif- ferences in the characters of the hairs and bristles of the bueca and the vibrissal ridge. That portion of the bucca which is on the occi- pital surface is bounded by distinct sutures. The whole bucca is hairy or bristly, the hairs and bristles varying in number and size in different species. Mesad of the arms of the frontal suture, constituting the lateral boundaries of the facial fossa, are two distinct ridges, one on each side of the face. These are the vibrissal ridges, so-called because on them the stout bristles called vibrissae are inserted. They were called the facialia by Desvoidy, by Walker and by Baron Osten- Sacken, but the term used by Professor Brauer, “ Vibrissenleisten,” meaning vibrissal ridges, is so much more appropriate, that I prefer to sacrifice priority to good sense. If we follow the vibrissal ridge dorsad we find that it diminishes in width and gradually disappears- from view under the gena. If we follow it ventrad we find that it gradually increases in width, being largest at a point called the vibrissal angle, where the largest of the vibrisse is inserted. The position of the vibrissal angle with relation to the edge of the mouth- opening is not the same in all genera, being sometimes very close to it and sometimes rather remote. In all the genera to be considered in this paper, however, except Pol/enia and Paracompsomyia, the two are very close together. Dorsad of the vibrissal angle we usually find one or more vibrissee which are much smaller than the one inserted at the angle. Dorsad of the smaller vibrisse the ridge is usually more or less thickly beset with minute bristles as far as or beyond the ventral end of the arm of the frontal suture. Ven- trad of the angle there are usually a few vibrisse. The bristles of the legs require also a few words of introduction. These bristles have not as yet received the study that they deserve in the Muscidw. I believe there is a typical arrangement of these 12 PROCEEDINGS OF THE ACADEMY OF -. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 171 bristles subject, of course, to great variation but easily recognizable. When the limbs of a Muscid are in their natural position it will at once be seen that so far as the fore and hind Jegs are concerned, one surface is turned toward the median line of the body and one away from it; these are the mesal and lateral surfaces respectively. The lateral surfaces are provided with stouter and more numerous bristles as would be expected if, as is supposed, the function of the bristles is a protective one. The terms flexor and extensor need no explanation. The anterior femur in cross section has the shape I, 1, and its bristles (at least the prominent ones) are in three rows, each of which extends from base to apex. ‘Two of these rows are near the extensor border, the one nearest that border being made up of larger bristles than the other; the third row is very near the flexor border; all three are on the lateral surface. The hind femur is shaped very like the fore femur, and has on its lateral surface an extensor row and a flexor row of bristles, corresponding to the row nearest the extensor border and the flexor row of the lateral surface of the fore femur; the mesal surface has also a flexor row, but its members are smaller and less numerous than those of the flexor row of the lateral surface. The middle femur is much less flattened than the others, and in its natural position its surfaces are anterior and posterior flexor and extensor; it has an anterior flexor and posterior flexor row of bristles and also an anterior median and a posterior median row. Asa rule the median rows are incomplete, i.e., do not extend all the way from base to apex. The anterior commonly ends half way from base to apex, the most apical mem- bers of the row being the largest, the posterior often begins about half way from base to apex, and extends thence to the apex, its apical members being also the largest, and usually the apical three or four form a transverse group of considerable prominence. The tibize are, in cross section, almost triangular with a very well marked extensor border and with flexor, mesal and lateral (middle tibia with flexor, anterior and posterior) surfaces. The same difference in size and number of bristles that was noted in the case of the mesal and lateral surfaces of the fore and hind femora is noticeable in the corresponding tibis, but is not so pronounced. Each of these surfaces has, ordinarily, a flexor and extensor row of bristles. The middle tibia has also flexor and extensor rows of bristles on its anterior and posterior surfaces, and it has, in some genera, a prom- inent bristle on the flexor surface which does not occur (as far as 172 PROCEEDINGS OF THE ACADEMY OF [1898.. my observation extends) on either of the other tibie, Very often the surfaces of the tibize have other rows besides the flexor and ex- tensor, such are usually made up of minute bristles, except for the terminal subapical member, but sometimes one or more of the mem- bers are largely developed and in consequence an oblique row of large bristles may appear on the tibia as in I, 2. The apical bristles of the tibiae are remarkably constant in num- ber, arrangement and relative size. Although the number of specimens collected by Dr. Smith in the group Muscidee (sens. strict.) is quite small, only thirty-eight, never- theless the collection is very interesting, including eleven genera, of which three are new, and thirteen species of which seven are new. Genus GLOSSINA. Glossina longipennis Corti. Two females taken August 19, 1894, and August 24, 1894. They agree perfectly with Corti’s description, except that there are no brown spots on the abdomen. Genus IDIA. Idia lunata Wied. Three females taken September 29, 1894, October 2, 1894, and November 10, 1894. Genus COSMINA. Cosmina sp. ? Female, taken November 10, 1894. Too imperfect to identify or describe. Genus MUSCA. Musca domestica L. Female specimen, taken October 11,1894. This is a variety with color and markings of abdomen somewhat like the male. The ground color is a dull reddish-brown, on each of the first three seg- ments there is a narrow, median, cephalo-caudal black stripe; the whole of the ventral surface of all segments and the cephalic half of the dorsal surface of the first segment are rather more yellow than the remainder of the dorsal surface. In color of abdomen the specimen reminds-me of a female specimen sent me by Dr. Wm. A. Nason, in which the abdomen had the color and markings of the male, Structurally the specimen is identical with domestica although it has, to be sure, five dorso-central bristles behind the suture, but 1898.] NATURAL SCIENCES OF PHILADELPHIA. 173 this number occurs occasionally in otherwise normal specimens both of domestica and corvina. ‘Musca corvina Fabr. One male taken September 10, 1894. Musca biseta nov. sp. One male and four females, all taken March 10,1894. Very much like domestica, from which it differs as follows: Male.—Front about one-half as wide as in specimens of domestica with the same width of head. Dorsum of first abdominal segment entirely black. Female.——Front of same width as that of specimens of domestica with same width of head, but the frontal vitta is decidedly narrower and its lateral borders less curved. Both Sexes.—Smaller than the average sized domestica. (Geno- vertical plates, gense, buccz and vibrissal ridges silvery white, with scarcely a trace of the yellowish tinge which so often predominates in domestica. Only two dorso-central bristles in front of the suture. Bristles of the extenso-lateral row of the hind tibia equal or almost equal. No prominent bristle in the extenso-mesal row of the hind tibia. Genus MORELLIA. Morellia podagrica Loew. Two males and one female taken March 10, 1894, and April 10, 1894. Agree perfectly with, but are smaller than, my European specimens of this species. Genus PSEUDOPYRELLIA. Pseudopyrellia «p. ” One male and one female taken March 10, 1894. This is a new species. The specimens are too imperfect to describe fully. The antennal arista has longer, more numerous and more delicate hairs than cornicina (American and European specimens), and the female has on the thorax, in front of the suture, a broad, median, cephalo-caudal hoary stripe which fades out before the suture is reached. The distinctness and brilliancy of this stripe vary with the incidence of light. Of 100 American female specimens of corn- icina examined not one has this stripe. The front of the male is much narrower than in cornicina. ‘Pseudopyrellia nuda nov. sp. Four females taken March 10, 1894, and September 29, 1894. Length about 8 mm., of a brilliant metallic violet color, varying to bronzy-green. Remarkably few and delicate macrochets. 174 PROCEEDINGS OF THE ACADEMY OF [1898. Width of head about 2.4 mm., of front about0.7 mm. Vitta occu- pies about one-third of the front. The genze and the ventral quarter or fifth of the geno-vertical plates are silvery-white or dead black, according to the incidence of the light, the remainder of the geno- vertical plates, the ocellar prominence and the dorsal half of the posterior orbit are metallic violet or green ; the ventral half of the posterior orbit is silvery white, dead black or with metallic reflect- ions according to the incidence of the light; the buccze are dead black or metallic violet according to the incidence of the light; the vibrissal ridges are black with slight metallic reflections ; the frontal vitta is dead black. The bristles of the vertex are as in cornicina ; the hairs of the geno-vertical plates (there are no orbital bristles). are as in cornicina, but much Jess numerous; the bristles of the vibrissal ridges are yellowish-brown and arranged as in cornicina ; the bucez are sparsely beset with delicate yellowish-brown hairs. Palpi black or dark brown, dilated at the apices; proboscis black or dark brown, with some metallic reflections. Antenna, 2d joint 0.2 mm., 3d joint 0.6 mm.; color brown, 3d joint lighter than 2d. The whole thorax and abdomen has a finely punctate appearance and is remarkably free from macrocheete, although quite as thickly clothed with fine hairs as is usual in the Muscide. Bristles of thorax.—I, 3a, 3b, 3c. Humeral, 1. Dorso-central, 4, 2 in front and 2 behind the suture, the posterior is of good size, the rest are minute. Jntra-alar,1, very small. Supra-alar, 1, very small. Post alar, 2, as usual, of good size. Notopleural, 2, as usual, of good size. Sceutellar, apical and two marginal, of good size. Tegule hyaline; Halteres pale yellow. Legs—Femora black or very dark brown, with some metallic reflections.. Tibise and tarsi black or very dark brown ; bristles of legs much smaller and less numerous than usual in the Muscide. Fore Leg.—Femur.—Only one extenso-lateral row of bristles, and this is made up of fewer and smaller bristles than usual. Bristles. of flexo-lateral row smaller and much fewer than usual. — Tibia.— No prominent bristles except the preapical of extensor border. Middle Leg—Femur.—The usual rows are present, but the indi- vidual bristles are small, and there are but few of them. The only respectable sized bristle of the femur is the preapical of the poste- rior surface. Tibia.—Anterior surface no bristles at all. Posterior surface.—One prominent bristle at the middle of the tibia and a varying number of other much smaller bristles. Flexor surface— 1898.] NATURAL SCIENCES OF PHILADELPHIA. 175 One large bristle, about twice as large as the largest of the posterior surface, at the junction of the third and apical fourths, inserted close to the edge of the posterior surface. Hind Leg.—Femur.—The usual rows present but of fewer and smaller bristles than usual. Tibia—No prominent bristles save one very delicate flexo-lateral. Genus POLLENIA. I might consider the species to be here described as the type of a new genus in deference to the views of Professor Brauer as ] under- stand them. He gives as one of the characters of Pollenia: ‘ two orbital bristles in the female.” These specimens have from four to six orbital bristles of large size inserted in a dorso-ventral line roughly parallel to the insertions of the trans-frontal bristles and laterad these large orbitals and parallel to them another row of very small bristles. I am sure that the number of large orbital bristles may vary in individuals of the same species and, therefore, am per- sonally of the opinion that their number is not always a character of generic value, e. g., in our common species of Morellia the num- ber of large orbital bristles varies from two to seven, frequently dif- fering on the two sides of the same specimen, Such being the case, it seems to me that I must include this species in Pollenia since it presents all the characters of that genus except the one mentioned. The woolly hair is present only on the caudal border of the meso- pleura, caudad the row of bristles which protect the root of the wing, a condition often met with in our common P. rudis if the specimen is not fresh. ‘The specimens look asif they had been wet. Pollenia virido-cana nov. sp. Three females taken September 5, 1895. Length about 7.5 mm. ; width of head about 2.2 mm., of front about 0.75, of frontal vitta about 0.25 mm. Looking at the head directly from in front, the height of the eye is 1.3 mm., of the bucca 0.4mm. The highest point of the vertex is a little higher (about 0.1 mm) than the high- est point of the eye. The third antennal joint is twice as long as the second. The general color of the fly is a dirty greenish-white or gray. On close examination it is seen that the ground color of the thorax and abdomen is a metallic green, but that this is more or less concealed by a thick, whitish, hoary coating. In some lights there seem to be two dorso-central bands on the thorax which are free from this 176 PROCEEDINGS OF THE ACADEMY OF [1898. coating. The anterior femora are of the same colors as the thorax, the middle and posterior femora are dark brown, with here and there suggestions of the green color and hoary coating. The tibize and tarsi are a very dark brown. Tegule milky white. Halteres brownish. The gens, geno-vertical plates, ocellar triangle, poste- rior orbits, buccz and vibrissal ridges are dirty white with the usual silky lustre, varying according to the incidence of the light to a pale brown. Frontal vitta pale brown. Antenne: second joint pale brown, third joint darker brown with hoary coating. Bristles of Head.—Inner vertical, outer vertical, greater ocellar, and ciliz of posterior orbit as in P. rudis. Lesser ocellar less numerous than in rudis, only three or two pairs. Ascending frontal, one, large. Transfrontal six to eight, mostly decussate over the nar- row vitta. Orbital: a row of four to six large bristles, the inser- tions of which are roughly parallel to the insertions of the trans- frontals; a second row laterad the large ones and parallel to them composed of very small bristles. Genz bare. Buccz with a series of stout bristles along the edge of the mouth opening and with the remainder of their surface sparsely beset with very fine hairs. Vi- brissal ridges with a very few hairs dorsad the principal vibrissa extending little or not at all dorsad the ventral end of the arm of the frontal suture. Bristles of Thorax, I, 5a, 5b, 5c. Humeral,3. Post-humeral, 2. Dorso central, 6, two in front of and four behind the suture. Acrostichals very small, one anterior and two posterior to the suture. Jntra-alar, 4, one in front of and three behind the suture; the most posterior is very small and a little mesad the line of the others. Supra-alar, 3, of which, as usual, the middle one is much the largest. Post-alar, 2, as usual. Notopleural, 2, as usual. Seutellar.—A. small bristle of the jugum, an apical, two marginal and a rather small discal. Bristles of Abdomen.—As usual in Muscidee (sens. strict.). The macrochaetz of the head and thorax and nearly all the minute bristles and hairs of the thorax and abdomen appear to be inserted at the centres of little black disc-shaped spots. Bristles of the Legs.—Too imperfect to be described. The only especially noteworthy feature that can be made out is a long, stout bristle at the middle of the anterior surface of the middle femur. This represents, apparently, the anterior median row of bristles of the middle femur that is so universally present in the Muscidz (sens. _ strict.) and is so well developed in P. rudis. oo) tp 3 oS +e eee eS gage = 16 1898.] NATURAL SCIENCES OF PHILADELPHIA. 177 Genus LUCILIA. Lucilia spinicosta nov. sp. One male and one female, taken March 10, 1894. Length: about 5.5 mm. (male) and 6.0 mm. (female). Width of head: male 2.0 mm. female 2.2 mm. Width of front: male 0.1 mm. at narrow- est part, females 0.8 mm., vitta of female 0.5 mm. Third antennal joint twice as long as the second. Color—The usual metallic green of Lucilize with some hoary re- flections. Legs yellowish-brown, femora much darker than tibize and tarsi. Tegule: inferior dark smoky brown almost black, supe- rior hyaline. Halteres yellowish. Genz, geno-vertical plate, pos- terior orbit, bucce and vibrissal ridges silvery-white. Antenne: second joint and base of third yellowish-brown, remainder of third chestnut-brown. Palpi yellowish-brown. Wings hyaline, slightly stained with yellowish-brown toward the costal border. On the costal border of the wing, basad of but very close to the end of the auxiliary vein, is a good sized spine. On both the upper and under surfaces of the wing the third longitudinal vein bears a number of minute spines, those beneath are four or five in number and much more delicate than those above, those above are ten or twelve in number and extend nearly to the small cross vein. Bristles of the Head.—As usual in Luciliz. Bristles of the Thorax.—l, 7a, 7b, 7c. Humeral,3. Post humeral, 2. Dorso-central, 5, 2 in front and 3 behind the suture. Intra alar, 4, one in front and 3 behind the suture. Acrostichal, 5, 2 in front and 3 behind the suture. Presutural, notopleural, supra alar and post alar as usual. Sceutellar, apical, 3 marginal and one discal. Sternopleura and mesopleura as usual in Luciliz. Bristles of Abdomen.—On hind border of second segment a num- ber of small appressed bristles. On hind border of third segment about twelve to fourteen larger and less appressed bristles. On the fourth segment about twelve not at all appressed quite good sized bristles both marginal and discal. In the male these bristles are larger than in the female. Bristles of the Legs—Fore Leg—Femur: as usual but dorsal lateral extensor row has only about six members. ‘Tibia: in the lateral extensor row there is in the male, but not in the female, a little basad the junction of middle and apical thirds one rather prominent bristle; in the lateral flexor row there is one large bristle at the junction of the apical and middle thirds ; in the mesal extensor row 178 PROCEEDINGS OF THE ACADEMY OF [1898. there are no prominent bristles; in the mesal flexor row there are about four prominent bristles and these are larger in female than in the male. Middle Leg.—Femur: as usual. Tibia: the anterior surface, a little apicad the middle, has one large bristle ; the posterior surface has two rather smaller, one at the middle and one near the apical end of the basal third ; flexor surface has one at about the junction. of the middle and apical thirds. Hind Leg.—Femur: as usual. Tibia: the lateral extensor row has from three to five prominent bristles and the mesal extensor row two, of which one is very near the middle and the other in the basal quarter; no prominent bristles in either flexor row. Genus PAROCHROMYIA. The species to be here described would find its place in the table of Brauer and Bergenstamm! between Ochromyia and Zonochroa. The eyes of the male are very close together but not in contact. and the male has no transfrontal bristles above the middle point be- tween the base of the antenne and the vertex. Both sexes have ocellar bristles. Both sexes have abdominal marochete at the sides of each segment, on the hind margin of the third segment (appressed and delicate), and on the fourth; the male also has some on the hind margin of the second but they are more delicate than those of the third. The female has one fair sized orbital bristle at the upper part of the geno-vertical plate and, extending ventrad from this, a series of very delicate, minute bristles or hairs which extend along the whole of the geno-vertical plate and on the gena about half way to the end of the arm of the frontal suture. In Girschner’s system I should place this species among the Cal- liphorinz with the description of which it agrees’ except that it has three posterior intra-alar bristles. The sterno-pleural bristles have the arrangement J-1. I can not make out the arrangement of the second ventral segment. Parochromyia varia nov. sp. Three males and three females, taken March 10, 1894, Nov. 17, 1894, Sept. 3, 1895. A pale yellowish-brown fly about 6.5 to 7.5 mm. long. The wings are notably broad and extend a little bey ond the apex of the abdomen. 1y orarbeiten zu einer Monogr., ete., Pars III, p. 90, (178). ? Separat-Abdruck aus der Pivetcdtcen Wochenschrift fiir Entomologie, Vol. I, 1896, p. 14. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 179 Head.—The antennz, bucesx, gene, vibrissal ridges, facial fossa and ventral third to half of the geno-vertical plate are all pale yellowish-brown. The remainder of the geno-vertical plate is bluish gray. The frontal vitta is brown with a slight reddish tinge. The posterior orbit differs in the two sexes. In the female it is about 0.1 mm. wide, bluish-gray dorsally and shading off ventrally to pale yellow; in the male it is narrower, entirely absent along the dorsal third or half of the eye and entirely yellow. In the female the front occupies about one-third of the width of the head and is mostly made up of the frontal vitta the geno-vertical plate being very narrow. Bristles of the head.—Female :—Seven to nine transfrontal of good size and a few small intercalary, sometimes the larger ones decussate and sometimes not, they extend a little ventrad the insertion of the antenne. Ascending frontal, one. Orbital as mentioned in the generic description. Greater ocellar, of good size, divergent. Lesser ocellar, several pairs all parallel to the greater; one very small pair is situated ventrad the greater, there are several sinall pairs dorsad the greater and one pair at the dorsal border of the ocellar triangle is half to three quarters the size of the greater. Inner vertical and outer vertical, inserted as usual, equal ; only a little larger than the ascending frontal, larger than the greater ocellar. Post vertical small, erect, parallel to one another, inserted on the occipito-vertical border a trifle caudad the line of the inner verticals. Occipito- central, very small and delicate, inserted very close to the occipito- vertical edge. Occipito-lateral not present. Cilise of posterior orbit rather sparse but well aligned, extending ventrad to the caudo- ventral angle of the eye. Bueca: vertical diameter as seen from in front nearly one half that of eye; along edge: of mouth-opening a series of large stout bristles, the remainder sparsely beset with min- ute hairs. Vibrissal ridges: a few minute bristles dorsad the prin- cipal vibrissa extending to a point a very little dorsad the ventral end of the arm of the frontal suture. Male:—Transfrontal, as mentioned in the generic description, about seven in number. Inner vertical good sized. Outer vertical absent as is usual in male Muscide. Greater ocellar much smaller than in the female (the usual thing in Muscide). Lesser ocellar, quite numerous, some of them almost equal to the greater. Post vertical as in the female. Occipito-central (doubled in one speci- men), ciliz of posterior orbit, bucca and vibrissal ridges as in female. Antenna.—Third joint about twice as long as thesecond. Arista 180 PROCEEDINGS OF THE ACADEMY OF [1898. longer than second and third joints together, its hairs rather few (about eight above and six below). The exact shade of color varies in different specimens, being sometimes darker and sometimes lighter; in one female the third joint is almost a chestnut-brown. Proboscis and palpi yellowish-brown. Thorax.—Color, varying shades of yellowish-brown, darker on the dorsum. On the dorsum, bands of dark brown or bluish-gray, vary- ing much in width in different specimens (in one male none at all). A dark spot on the middle of the scutellum in all the females and in one male. Bristles of the Thorax, 1, 9a, 9b, 9c. Humeral, 3. Posthumeral, 3, outermost on a level ventrad the presutural. Dorso-central, 6, two in front and four behind the suture. Jntra-alar, 4, one in front and three behind the suture. Acrostichal, 6, three in front and three behind the suture. Presutura/, notopleural, supra-alar and post-alar as usual. Post-sutwral, I venture to apply this name to a bristle, present in all the specimens of this species, which I have not been able to find in any other Muscids that I have seen. It is situated caudad the transverse suture of the thorax, a little mesad and cau- dad the anterior supra-alar, and laterad the intra-alar No. 3 (1 num- ber the intra-alars, dorso-centrals and acrostichals from the caudal end of the thorax cephalad, thus the intra-alar nearest the scutellum_ is No.1). Scutellar—Apical, three marginal, jugal, two discal of which the anterior is considerably the larger. Abdomen.—Color: Principally yellowish-brown; of varying shale in different specimens. There are also some very dark brown, al- most black, markings as follows: on the first segment a very nar- row band on the hind margin; on second segment a broader band and a median mark, (I, 11) the width of the band and the size of the mark varying considerably ; third segment like second, but the band broader and the mark larger, so that in some specimens almost the whole segment is dark brown or black: fourth segment entirely black or dark brown. Bristles—There are bristles on the hind borders of the first three segments. Toward and at the sides of the segments the bristles are larger than toward the middle. All are more or less appressed. Those toward the middle can hardly be called macrochaetae until we reach the third segment. On the fourth there are some discal as well as marginal macrochaetae, and they are none of them ap- pressed. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 181 Legs.—Color: Yellowish-brown. Bristles: Fore-leg, femur, as usual. Tibia, lateral flexor row has one large bristle at the junction of the middle and apical thirds, mesal extensor row has from four to six rather small bristles about equal and equi-distant, extending from very near the base to very neartheapex. Middle leg: Femur, as usual, but the anterior median row is represented by only one bristle of good size which is situated just at the middle of the femur. On the whole, the bristles of this femur are rather few. Tibia: An- terior surface, one large bristle at junction of apical and middle thirds ; posterior surface two, rather smaller at junction of basal and middle, and middle and apical thirds respectively; flexor surface one, rather small at junction of apical and middle thirds. Hind leg = Femur, as usual. Tibia, mesal extensor row has usually two promi- nent but not very large bristles situated respectively at the junction of the basal and middle, and middle and apical thirds (sometimes the former is absent); lateral extensor row has a considerable but varying number of unequal but almost equidistant bristles extend- ing from base to apex; lateral flexor row is represented by only one bristle situated at the junction of the apical and middle thirds. Genus SOMALIA. There is but a single specimen, and that a female of the species on which I found this new genus, but the characters are so pro- nounced that I have no hesitation in so doing. In the table of Brauer & Bergenstamm’ this genus would fall in the group with Dasyphora, except that it has but one large orbital bristle. It dif- fers, however, from Dasyphora in several points: (1) the sterno- pleural bristles have the arrangement 2-1, instead of 1-3; (2) there is a row of bristles on the hypo-pleura; (3) the third joint of the antenna is much shorter as compared with the second; (4) the out- line of the arista as a whole is much narrower, and its hairs are less closely set; (5) the eyes are only minutely hairy with a magnifica- tion of twenty diameters; (6) the post-vertical bristles are very small, while in Dasyphora they are large. In Girschner’s classification the new genus stands far away from Dasyphora in the 6th or 7th group of his Tachinide. Somalia enigmatica nov. «p. One female, taken October 11, 1894. * Vorarb. zu Monog. Muse, Schiz., Part 11], p. 90 et seq. 182 PROCEEDINGS OF THE ACADEMY OF [1898. Length about 8.0 mm. Width of head 2.5 mm., of front 0.9mm. (vitta 0.5 mm., geno-vertical plates each 0.2 mm.). Looked at squarely from in front the dorso-ventral diameter of the head is 2.3 mm., the vertex extends 0.1 mm. dorsad the eyes, the dorso-ventral diameter of the eye is 1.5 mm., of the bucca 0.7 mm. Third anten- nal joint about 14 times as long as the second. General color pale olive-green with a hoary coating, legs a yellowish-brown, except that the third, fourth and fifth tarsal joints and the apical part of the second are black. On the thorax, in front of the suture, are two narrow bands, one on each side, between the acrostichal and dorso- central bristles, which have no hoary coating ; these bands broaden cephalad and unite at the cephalic border of the thorax. On the second, third and fourth abdominal segments there is a narrow, median, cephalo-caudal dark brown stripe not represented in the diagram, I, 15, which shows also the arrangement of the abdominal bristles. Head.—Color: Genae, geno-vertical plate, facial fossa, vibrissal ridges, posterior orbits and ocellar prominence silvery; vitta dark brown; bucea olive; transverse impression of the face yellowish- brown with silvery coating. Second joint of antennz yellowish- brown, third joint darker with a hoary coating. Palpi yellowish- brown. Proboscis black. Bristles: Trans-frontal, about eight, of which the ventral four or five are of good size and inserted close together, the rest small and scattered. Ascending frontal, one, large. Orbitals, one large at about the junction of the dorsal and middle thirds of the front and one exceedingly minute a little dorsad the large one, no others at all. The bristles at the vertex are somewhat injured, and I can only say that the inner vertical, outer vertical, greater and lesser ocellar, post-vertical (very small), and ciliae of the posterior orbit are present ; nothing unusual can be made out in regard to them in this specimen. Genz naked. Bucce distinctly separated from the vibrissal ridges; parallel to the edge of the mouth-opening and a little distance from it is a row of coarse bristles; near the cephalic end of the bucca about as far dorsad the large bristles of the mouth- edge as they are from the mouth edge itself, are two stout bristles about equal in size to those of the mouth edge; the rest of the bucca is rather sparsely beset with minute bristles and hairs. Vibrissal ridges: The principal vibrissa and the vibrissal angle are close to the edge of the mouth opening; dorsad the principal vibrissa there 3 es 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 183 are only a few minute bristles not extending as far as the ventral end of the arm of the frontal suture; ventrad the principal vibrissa are four lesser vibrissz inserted along the edge of the mouth opening as far as the cephalic end of the bucca. Thorax.—Color, as mentioned above. Halteres yellow. Tegule hyaline, milky white toward the edges. Bristles, I, 15a, 15b, 15c. Humeral,2. Posthumeral,1, on a level dorsad the presutural. Dorso-central, 5, two in front and three be- hind the suture. Jntra-alar, 3, none in front of the suture. Acros- #ichal, 2, one in front and one behind the suture, both small. Presu- tural, notopleural, supraalar and postalar as usual. Seutel/ar: apical, two submarginal and one small discal or subapical. Mesopleural. At the dorso-cephalic angle is a group of little hairs, among which two are more prominent than the rest, and per- haps deserve to be called bristles, an arrangement recalling the prominent bristle in this situation which is so constant in the genera Morellia, Muscinia, Musca, Myospila and their allies. As usual, there is a large bristle just ventrad the prostigma, a little ventrad and caudad this bristle is another, much smaller but decidedly promi- nent, which I have not found in any other Muscid. Sternopleural. Two in front and one behind. Pteropleural and Aypopleural present. Wing. Venation shown in the figure. On the third longitudi- nal vein are about ten little spines quite regularly distrlbuted from the base to near the small cross vein. There is a costal spine just basad the end of the auxiliary vein. Ventral surface of abdomen. Nb ventral membrane; second ventral segment overlaps the edges of the corresponding dorsal, all the other ventral segments are overlapped by the corresponding dorsal. fox, C71 C9 tel “CS paw IE ta ES Il. Bristles of the Legs.—Anterior femur as usual. Anterior tibia: lateral flexor row has one large bristle at the junction of the middle 184 PROCEEDINGS OF THE ACADEMY OF (1898. and apical thirds; mesal extensor row has three prominent bristles as arranged in II, 1. Middle femur has one large bristle at the middle of the anterior surface, a few bristles in the flexor row of each surface, and on the posterior surface a subapical transverse group of three. Middle tibia has one on the anterior, II, 2, three on the posterior, II, 3, and one on the flexor, II, 4, surface. Poste- rior femur as usual. Posterior tibia has four on the lateral surface (two flexor and two extensor, IL, 5), and two on the mesal surface II, 6. Genus PARACOMPSOMYIA. Very close to Compsomyia. In the table of genera of Brauer and Bergenstamm it would fall with Compsomyia from which it differs as follows: wings not hyaline but, toward base and costa, black or very dark brown ; thorax without longitudinal black stripes ; the vibrissal angles are not as far dorsad the mouth edge as in Compsomyia; there are no vibrissee ventrad the principal vibrissa; the orbital bristles are much smaller than in Compsomyia and are directed laterad instead of ventrad ; the sterno pleural bristles are 1-1 instead of 2-1. Paracompsomyia nigripennis nov. sp. Four females, taken August 23,1894. Large metallic blue, violet or green flies with yellow heads, black legs and with the costal border and basal half of the wings black or very dark brown. Length of body 11 to 12 mm., of wing 10 mm. Width of head 5 mm.; of front 1.7 mm. at base of antennz, 1.8 mm. at vertex ; fron- tal vitta 1 mm. at widest point, 0.7 mm. at base of antenne. Looked at squarely from in front the dorso-ventral diameter of the head (height) is 4.2 mm., the vertex extends 0.2 mm. dorsad the dorsal border of the eyes, the dorso-ventral diameter of the eye is 2.5 mm., of the bucca 1.5 mm. The second antennal joint is 0.8 mm. long, the third is 1.1 mm. Head.—Color :—dorsal two-thirds of geno-vertical plate is polished ferruginous, the ventral third as also the genz, bucce, vibrissal ridges and facial fossa are a paler, yellowish-brown with a thin hoary coating. Vitta ferruginous. Antenne yellowish-brown. Ocellar prominence and an adjoining triangular area of varying size at the dorsal part of the occiput ferruginous to yellowish-brown varying in different specimens. Posterior orbit silvery. Palpi yellow. Proboscis dark brown to black. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 185 Bristles.—Inner vertical and outer vertical of good size, inserted as usual. Post vertical very small, inserted a little caudad the line of the inner verticals. Occipito-central replaced by a number of minute bristles. Cilize of posterior orbit as usual, well aligned, rather small. Greater ocellar very small, divergent, pointing almost directly laterad. Lesser ocellar exceedingly minute, numerous, in four to six rows, occupying nearly the whole of the ocellar promin- ence and extending caudad to or nearly to the line of the inner ver- ticals. Ascending frontal, one, parallel to the outer vertical, in- serted on a level with the greater ocellar some distance laterad the line of insertion of the transfrontals half way between that line and the lateral border of the geno-vertical plate. Transfrontals ten to twelve, sma!l, non deccusate. Orbitals two, very small (0.2 to 0.3 mm. long), curved laterad instead of ventrad as usual, inserted III. Humeral, 3. Dorso-central, 5, 2 in front of and 3 behind the suture. Intra-alar, 1. Supra-alar, 2. Acrostichal, 1, posterior. Presutural, notopleural and postalar as usual. Seutellar : Apical, four marginal and two discal as figured. about at the middle (dorso-ventrally) of the geno-vertical plate and 0.3 or 0.4 mm. (dorso-ventrally) from each other; besides these two orbitals the geno-vertical plate is quite thickly clothed with very minute hairs or bristles which toward the vertex are black and toward the gen are whitish or colorless. Gen, clothed like the geno-vertical plates with exceedingly delicate and minute whitish hairs. Bucew clothed like the gene, but toward the occiput the hairs are much longer than elsewhere (as much as 0.2 mm.). Vi- brissal ridges almost straight, only very slightly convex laterad; 13 186 PROCEEDINGS OF THE ACADEMY OF [1898. vibrissal angle and principal vibrissa a little above the mouth edge but not as high as in Compsomyia macellaria or in Pollenia; the principal vibrissa is very small for the size of the fly; there are no other vibrisse but the ridges are clothed nearly their whole length with exceedingly minute whitish hairs. The arista is about as long as the third antennal joint and is densely plumose with fine hairs. Its rhachis is yellow toward the base while its apical part and the hairs appear black. Thorax.—Color.—Metallic blue, violet or green with hoary coat- ing. The hoary coating is much thicker in front of than behind the suture. The prostigma is very large and is white. Halteres yellow- ish. Tegule white with smoky brown or black border of very vary- ing width. Bristles—There is a row of bristles on the hypopleura and some bristles on the pteropleura. Abdomen.—Color.—Metallic blue, violet or green with a hoary coating which is thickest toward the sides and on the ventral sur- face. The first segment and the caudal borders of the second and third are not hoary. The fourth segment is quite thickly covered with whitish hairs. There are no abdominal macrochete. The second yentral plate overlaps the corresponding dorsal plates a very little, the other ventral plates are overlapped by the corresponding dorsal plates. Bristles of the Legs.--Femora as usual in the Muscide. Tibiz: anterior tibia has on the mesal surface in the extensor row three prominent bristles III, 4, and on the lateral surface in the flexor row one III, 5; middle tibia has on the anterior surface one III, 6 on the posterior surface three III, 7, and on the flexor surface one III, 8; hind tibia has on the lateral surface in the flexor row two III, 9, and on the mesal surface, in the extensor row, one III, 10. EXPLANATION OF FIGURES. 1. Cross section of anterior femur of a Muscid. 2. Formation of an oblique row of bristles on the tibia. 3a. Bristles of thorax of Pseudopyrellia nuda nov. sp. 3b. Bristles of sternopleura of Pseudopyrellia nuda nov. sp. 3c. Bristles of mesopleura of Pseudopyrellia nuda nov. sp. 4. Wing of Pseudopyrellia nuda nov. sp. 5a. Bristles of thorax of Pollenia virido-cana nov. sp. 5b. Sternopleura of Pollenia virido-cana nov. sp. 5c. Mesopleura of Pollenia virido-eana nov. sp. det i @ 1898.] NATURAL SCIENCES OF PHILADELPHIA. 187 6. Wing of Pollenia virido-cana nov. sp. 7a. Bristles of thorax of Lucilia spinicosta nov. sp. 7b. Sternopleura of Lucilia spinicosta nov. sp. 7c. Mesopleura of Lucilia spinicosta nov. sp. 8. Wing of Lucilia spinicosta nov. sp. Ya. Bristles of thorax of Parochromyia varia nov. sp. 9b. Sternopleura of Parochromyia varia nov. sp. 9c. Mesopleura of Parochromyia varia nov. sp. 10. Wing of Parochromyia varia nov. sp. 11. Marking of abdominal segment of Parochromyia varia. 12. Arista of Somalia enigmatica nov. sp. 13. Abdomen of Somalia enigmatica nov. sp. 14. Wing of Somalia enigmatica nov. sp. 15a. Bristles of thorax of Somalia enigmatica nov. sp. 15b. Mesopleura of Somalia enigmatica nov. sp. ; 15c. Sternopleura of Somalia enigmatica nov. sp. L Diagrams of positions of bristles of tibise of Somalia enigmatica. 1. Anterior tibia; mesal surface, extensor row. 2. Middle tibia; anterior surface. 3. Middle tibia; posterior surface. 4. Middle tibia; flexor surface. 5. Posterior tibia; lateral surface. 6. Posterior tibia; mesal surface. II. 1. Antenna of Paracompsomyia nigripennis nov. sp. 2a, 2b, 2c. Thorax, mesopleura and sternopleura of same. 3. Wing of same. 4 to 10 positions of bristles of tibize of same. 188 PROCEEDINGS OF THE ACADEMY OF [1898. A NEW WEASEL FROM NEW MEXICO. BY C. M. BARBER AND T, D. A. COCKERELL. Putorius frenatus subsp. neomexicanus n. subsp. Similar to P. frenatus, but paler in color; white markings on head more extensive, the white patch between the eyes large, quad- rangular, and confluent with the stripes between eye and ear. Color—Upper parts, including legs and body from shoulders to tail, entirely of a uniform pale yellowish ochre, a sort of dilute coffee color, but warmer; feet decidedly pallid, but not white. Tail the color of the back, but rather more tinged with reddish, the apical 50 mm. black. Under parts, including breast and throat, uniform light yellowish-ochreous, a tint like that of the back but somewhat paler. Head brownish-black; a large quadrangular creamy-white patch between the eyes, slightly broadest behind, about one-fifth longer than its greatest breadth, narrowly confluent with broad white bands between the eye and ear, which latter ex- tend downward and backward, fading gradually into the ochreous color of the under parts. Face in front of median white patch slightly speckled with whitish. Long bristles of upper lip, some black and some white ; a variable amount of white on upper lip; no black behind angles of mouth. Hair of ears brown-black, but white hairs from the lateral bands invade the lower anterior parts, over- lapping the aperture. The black of the head fades into brown be- hind the plane of the ears, and shows here a small whitish mark; the area behind the lower part of the ears is strongly suffused with blackish, contrasting with the yellowish-white immediately below. Cranial characters.—Compared with Merriam’s figure of the skull of frenatus (N. A. Weasels, Pl. III, f. 1), the skull of neomexicanus is similar, but the frontal region is less narrowed anteriorly and slightly more convex ; and the zyomatic processes seem less produced in a lateral direction ; the occipital condyles are more produced be- hind. Total length of skull 54 mm.; greatest breadth 32; interorbital breadth 14} ; foramen magnum to plane of last molars 34 mm. Measurements (of type specimen in flesh)—Length 500 mm., tail 205, hind feet 50. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 189 Hab.—The Mesilla Valley of New Mexico, near the Rio Grande, alt. about 3,800 ft. The type specimen was shot in the grass on the shore of Arm- strong’s Lake, Mesilla, Feb. 1, 1898, by Mr. A. C. Tyson. It is an old male; the teeth are somewhat worn and one or two are gone. It had eaten some small rodent, which from the foot found in the stomach seems to be Onychomys arcticeps Rhoads. A second speci- men, also a male, was given to us by Mr. C. Barnes, who obtained it from Mr. J. J. Roese. It was killed by a dog in Mesilla Park, and was, unfortunately, much decomposed when it reached our hands. It agrees with the typical specimen, except that the throat is whiter and there is a little more white on the upper lip. Mr. Roese reports that he recently saw four specimens together in a road, early in the morning; this, with the development of the sex- ual organs, leads us to believe that this (beginning of February and end of January) is the mating season. A specimen without any history, in alcohol, is in the collection of the New Mexico Agricultural College. It approaches true frenatus more than our examples, having a spot behind the angle of the mouth, and the white median patch of the head confluent only on one side with the lateral band. The discovery of P. frenatus neomexi- canus extends the range of the frenatus series many hundreds of miles to the north, and into the Upper Sonoran Zone. One of us, after reading Dr. Merriam’s account of the North American weasels, prophesied that there would be a new type found in the Mesilla Valley, and such proves to be the case, the characters of our ani- mal, while surely of no more than subspecific value, being quite distinct. 190 PROCEEDINGS OF THE ACADEMY OF [1898. ON THE GENUS HALIA OF RISSO. BY WM. H. DALL. The systematic position of the genus Halia, a curious deep water gastropod discovered in the last century, has long been contested. Lamarck (who knew it only by the shell) put it among the land- shells like Achatina, Martyn referred it to the whelks (Buccinide), Jay and Sacco classified it in the vicinity of Struthiolaria, and Sowerby near Purpura. Fischer, in 1858, was the first to examine it anatomically and concluded that it was one of the Towifera, related to Pleurotoma. The paper was one of his earliest and rather crude; though it added materially to our knowledge, the conclu- sions were not altogether satisfactory to students of molluscan anatomy. Nevertheless his view has been accepted so late as 1896 by M. Cossmann, one of the leading paleontologists of France. In 1885 Poirier, of the Paris Museum, was lucky enough to obtain a specimen, a female, like that of Fischer, dredged in fifty fathoms at the mouth of the Gambia River. His discussion of the dis- section’ added very considerably to our acquaintance with the macroscopic anatomy and that of the nervous system, He was, however, little less unfortunate than Fischer in his examination of the most important systematic character, the radula, and reported an extraordinary duplication of the cesophagus, such as is quite un- known elsewhere in mollusks, and which would require the most conclusive confirmation to receive credence from anatomists. Poi- rier reverted to the opinion of Martyn that Haldia is Buccinoid, which being interpreted into systematic language, means that he recognized in it the characteristics of a rhachiglossate Prosobranch, which is essentially correct. The true relations of this remarkable form were first recognized by Kobelt in a later publication? which has unfortunately remained unfinished and has attracted no atten- tion from anatomists. In view of the fact that the early errors have obtained such a wide currency and that, even in Fischer’s Manual, the characters of the nearest allied form are incorrectly 1 Bull. Malac. Soc. de France, July, 1885, pp. 17-50, pl. II-IV. 2 Inconographie der schalentragenden europ. Meeresconchylien, II, p. 6. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 191 given, it seems worth while to restate the latest and most trust- worthy conclusions. Each tooth of Halia is shaped much like a “wish-bone,” the prongs forming an arched divergent base and the central projecting portion at the junction, the cusp. The attached bases of the arch are turned up a little and indistinctly notched on the edges; the main part of the arch is free and very prominent. When the cover glass of the microscopic slide is pressed down upon the radula the pillars of the arch break away from the cusp at their junction, which led Poirier to regard them as a separate series of lateral teeth on each side, and Fischer, not noticing Troschel’s explanation of this part of one of his figures, has been led into the same error in regard to the analogous radula of Volutomitra. Poirier took the notched bases of the broken off lateral portions of the single tooth as the distal ends or cusps of his supposed laterals, directly revers- ing their true position. There is only a single row of teeth. The position of Halia is unquestionably among the Volutacea. The radula of Scaphella Turneri as figured by Gray, is almost iden- tical, and that of Volutomitra gronlandica is closely similar. Halia wants the siphonal appendage of the typical Volutes and so does Volutomitra. Both Scaphella and Volutomitra are without oper- cula, like Halia. The external form of the foot and head is essen- tially similar in all three. The texture of the shell of Halia, and also its color and color-pattern, are essentially identical with those of Seaphella (Aurinia) dubia Brod., which has the pillar and plaits degenerate. The process of degeneration, aided by the more ample whorls of Halia, has completed the effacement of the plaits and the enfeeblement of the pillar or central axis of the shell. The speci- men of Halia at my disposal for study is somewhat worn at the apex, but the form of the nucleus indicates that, like Seaphell/a and Volutomitra, its nepionic shell was membranous, and has left a rough scar on the surface of the initial shelly coil, a view confirmed by Cossmann’s figure of the nucleus of a fossil species. In Aurinia the degenerate radula is edentulous, but the type, which began in the Eocene, and has retained its color pattern and general charac- ters ever since, is abundant in the Pliocene, and may readily have thrown off the aberrant Halia at that period from which it is known to date. Halia was erected into a family by Kobelt, but it can hardly be said to possess family characteristics, its essential features being 192 PROCEEDINGS OF THE ACADEMY OF [1898. negative and due to degeneration from the normal type of the group to which it belongs. The characters of the latter, however, fully justify us in separating, from the operculate Volutide with their calcareous nepionic shell and Buccinoid dentition, the family Scaphellide, destitute of an operculum, with a membranous nepionic shell and the peculiar dentition above described. This latter group will include Caricella, Scaphella, Cymbiola, Eopsephea, Aurinia, Halia, Volutomitra and their allies. The recent Halia has been dredged along the eastern margin of the Atlantic from the Bay of Biscay to Senegal. The genus is re- presented in the Pliocene of Italy by one or two forms which have received distinct specific names, The type was first named by Meuschen in the Museum Gronovianum in 1778, and was erected into a separate genus by Risso in 1826, 1898.] NATURAL SCIENCES OF PHILADELPHIA. 193 DESCRIPTION OF A NEW TETHYS (APLYSIA). BY E. J. LETSON. Tethys Pilsbryin.sp. Plate VIII. _ Length 114 em., body elongated, flabby, plump, enlarged behind. Mouth encircled by wide lips and large buccal appendages. Rhino- phores (posterior tentacles, ) stout, short conic, slit at the extremities ; eyes small, black, placed before the rhinophores. Anterior ends of pleuropodial lobes well separated, posterior ends joined behind, mantle large, median perforation very small, surrounded by radial strize (visible only under a lens). Right margin of manile, folded over about half its width, and largely adnate; posteriorly not forming an excurrent siphon; gill considerably exposed. Genital opening under forward right border of mantle, surmounted by a fleshy prominence. Opening of opaline gland large, single, about 13 mill. back of the genital pore, and well under the gill. Gills foliated in regular branches. External integument smooth; with a few inconspicuous scattered warts; olive colored, with some cloud- ing of black on the reflexed mantle and sometimes also near the tail; shell normal. Silam, North Coast of Yucatan, (Heilprin). This differs from all other known species in having the mantle folded back upon itself and adnate except near the edge. 194 PROCEEDINGS OF THE ACADEMY OF [1898.. A NEW GRASSHOPPER MOUSE FROM NEW MEXICO. BY SAMUEL N. RHOADS. Among the ten species and races of short-tailed mice of the genus. Onychomys known to inhabit the United States we find a surpris-- ingly small amount of color variation, or of difference in size aemdb external proportions, from the type of the genus, O. leucogaster, from Dakota. The short, nearly unicolor, blunt tail, rounded, miervetime-. ears, dense, silky pelage and buffy gray colors are more or less ebsur- acteristic of all the species ranging from the Saskatchewan te the Mexican boundary. A careful study of their cranial characters is thus necessary im determining their relationships. A specimen of Onychomys in superficial appearance almost identa-. eal with /eucogaster, was recently forwarded to the writer from Me- silla, Dona Ana Co., New Mexico, by Mr. T. D. A. Cockerel), far- identification. Four specimens of Onychomys from Clapham, Unaem. Co., New Mexico, prove to be identical with the Mesilla specimem. and on comparison with their nearest geographical allies, /eweogas- ter, brevicaudus and longipes prove to belong to a distinct and wm. described species. It may be known by the following diagnosis :—- Onychomys arcticeps sp. nov. Long-Nosed Grasshopper Mouse, “Onychomys leucogaster subsp.?”” ; Allen, Bull. Amer. Mus, N. H., 1858. p. 74. “Onychomys leucogaster brevicauda’’; Allen, ibid, 1896, p. 25% Type No. 1,529, ad. 3, col. of S. N. Rhoads, taken by E. E.. Thompson at Clapham, Union Co., New Mexico, Nov. 7th, 1893 General characters.—About the size of leucogaster, with shighthy longer tail and ears, deeper fulvous (less gray) coloration abowe,. narrower cranium, and long, slender rostrum. Color—Above uniform ochraceous buff,’ heavily lined with black- ish, lightest along sides, blackest on top of head and around eyes. A blackish oval spot on upper, outer margins of ears. Tail white, with an ill-defined, narrow stripe of blackish-buff on superior prom imal two-thirds. Color of sides at the white margin and on lower rump and thighs deeper ochraceous buff. ‘Lower parts tawny white- as contrasted with the clear, pure white of leucogaster. 1 Ridgway’s Nomen. of Colors, Pl. V, No. 10. « @ % 4 © @ eek he dite 22s a 1898.] NATURAL SCIENCES OF PHILADELPHIA. 195 Cranial characters—Skull viewed from above (contrasted with leucogaster), long and narrow, the brain case high, compressed, elongate, ovate; the rostrum much narrowed and the nasals slender and projecting decidedly beyond the anterior tips of the premaxil- laries. No distinct supraorbital bead as contrasted with longipes from Texas. Palate ending posteriorly with a convex edge as in torridus, as contrasted with the strongly developed median spine of leucogaster. Measurements (of type).—Total length 150 mm.; tail vertebre, 45; hind foot, 21; ear, from crown (dry), 11. Average of four topotypes, in same order as above: 152—46—22. Skull: total length, 28.6; nasal length, 11.5; zygomatic expansion; 14.7; mas- toid expansion, 12; interorbital constriction, 4.7 ; length of mandi- ble 15.3. 196 PROCEEDINGS OF THE ACADEMY OF [1898. NOTES ON THE FOSSIL WALRUS OF EASTERN NORTH AMERICA. BY SAMUEL N. RHOADS. In the eleventh volume of the Transactions of the American Philosophical Society,’ Dr. Joseph Leidy describes and figures two specimens of fossil walrus obtained on the coast of New Jersey, and discusses the relationships of the recent and fossil forms of Atlantic walrus. In his opinion there is no foundation for a distinction be- tween the existing species and the so-called Trichechus virginianus of DeKay,’ based on a fossil walrus skull from Accomac County, Virginia. Iu the eighth volume of the Journal of the Academy of Natural Sciences of Philadelphia, published twenty years subsequent to his paper in the Transactions of the Philosophical Society above re- ferred to, Dr. Leidy describes a walrus tusk from the phosphate beds of Ashley River, South Carolina. This specimen he compares with the tusks of a large skull in the museum of the Academy from Nova Seotia, and concludes that the characters of the South Caro- lina specimen are not of sufficient value to determine whether it per- tained to a species distinct from the living one. The specimen from Nova Scotia, thus casually referred to by Dr. Leidy, is yet in the museum of the Academy, and is by far the most complete fossilized cranium of an adult animal of which we have any record. Before passing to a further consideration of the specimens de- scribed by Leidy, it should be stated that Dr. J. A. Allen, in his Me- moir of the Pinnipeds® also records‘ a skeleton of a fossil walrus “with tusks over five inches long” in the quaternary clays of Port- land, Maine. Dr. Allen does not seem to have examined any fossil specimens of walrus, nor does he venture an opinion as to the specific value of the so-called fossil species. From his full quota- tions of Leidy, however, it is evident that Dr. Allen was inclined to coincide with the determinations of so eminent an authority. ' New Series, pp. 83-86, pl. 4, and 5. * Nat. Hist. N.- York, Zool., I, p. 56, pl. 19, ftg. 1, a, b. ?7U. 8. Geol. Surv., Misc. Pub , XII, 1880. *See also Amer. Nat., Sept., 1878, p. 633. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 197 With the specimen from Nova Scotia above alluded to is a mem- orandum, evidently penned by the sender and donor of the specimen. It reads :—“ Office of School Commissioners, 48 George Street [ Hal- ifax], 187[1]. Skull of a walrus (Trichecus rosmarus) Sable Island, Nova Scotia. The walrus is now extinct in Nova Scotia. It was last seen alive on Sable Island sand beaches. There must have been a considerable number on the island, as a great many of their skulls have been thrown up on the beaches at intervals after heavy gales. The specimen sent was found some two years since, and as none have been found since then, I am inclined to think it the last of the series. You will observe that the tusks are partly fossilized.— J. R. W[illis].” This specimen is recorded in the Pro- ceedings of the Academy for 1871, and classified among recent ver- tebrate material. ‘This fact and the tenor of Dr. Leidy’s remarks regarding it show that he did not consider it a fossil. This is re markable, as the specimen is of precisely the same nature in color, texture and specific gravity as the larger fossil specimen which Leidy described and figured in the Philosophical Transactions, and which came from the beach at Long Branch, New Jersey. Un- doubtedly the Sable Island specimen is of the same age and deriva- tion from an ancient raised sea beach stratum as were the two speci- mens obtained on the shores of New Jersey, the skeleton from the quaternary clays of Portland, Maine, and the type of DeKay’s Trichechus virginianus from the sea beach of Accomac County, Vir- ginia. For this reason all of these fossil specimens are taken in the following study as typical of the supposed fossil species of Atlantic walrus as compared with the animal now existing on our North Atlantie Coasts of America. Of the four fossil specimens mentioned, three are now in the cus- tody of the Academy of Natural Sciences, the one from Sable Island and the more perfect of the two New Jersey specimens figured by Dr. Leidy, being the property of the Academy. The third specimen is the anterior half of the cranium from Long Branch, loaned to Dr. Leidy by Prof. Geo. Cook, and figured in the T'ransactions of the Philosophical Society. It was recently purchased from Prof. Ward of Rochester, N. Y., by the New Jersey Geological Survey for its museum at Trenton, and through the courtesy of Prof. J.C. Smock, was loaned to Mr. Lewis Woolman, of Philadelphia, for use in this connection. It is to the efforts of Mr. Woolman and his scientific interest in the work of the Survey, as well as his devotion to original 198 PROCEEDINGS OF THE ACADEMY OF [1898. research in the Academy of Natural Sciences that the facts con- tained in this paper are now made accessible. Mr. Woolman’s at- tempt to locate DeKay’s type of 7. virginianus resulted in the dis- covery that this specimen was destroyed by fire with the other ob- jects of natural history in the museum of the old New York Lyceum of Natural History, now known as the New York Academy of Sci- ences. The loss of this specimen, together with the inadequate descrip- tion of its characters and the crude nature of DeKay’s figure of it make the use of the name virginianus for an extinct species of wal- rus questionable, even in the event of proof that the other fossil speci- mens represent a different species from that now existing. However, if the characters of these latter can be shown to indicate such a state of affairs and at the same time show no radical differences from what we know of the type of virginianus, it is eminently proper that that name should be applied to them, and the extinct walrus of the glacial period be so distinguished from Rosmarus rosmarus. As Leidy has already shown, DeKay’s brief diagnosis of virgin- ianus’ is equally applicable to Rosmarus rosmarus, and had he not figured the specimen, we would now, on account of the loss of the type, be forced to make virginianas a probable synonym of rosmarus, The fact, however, that the type was a fossil and was figured, and that it, in all probability, represented the same species as the fossil skulls from New Jersey and Sable Island, makes the name as tena- ble as ever for a possible species of fossil walrus. The characters of all the fossil specimens show conclusively their closer affinity to rosmarus than to obesus of the Pacific Ocean, ex- cept in the relative size of the molars, In this respect they ap- proach more nearly the Pacific species as represented in the skull of an old male from Alaska, in which the molars are very large and rounded. ‘The canine tusks of the fossil specimens are characteris- tic of the rather short, heavy, decurved and spreading form seen in rosmarus. In respect of the ratio of the extreme facial width across the maxillaries to the greatest occipital width, it is noticeable that the fossil specimens come much nearer to obesus, in which the differ- ences between these dimensions are much less than in rosmarus. In the fossil specimen from Nova Scotia the maxillary expansion is 203 mm., and the paroccipital expansion (adding 10 mm. for wear) 5It reads: ‘ Cheek teeth with obliquely truncate crowns, not ridged; the second smaller than the first.” 15898.] NATURAL SCIENCES OF PHILADELPHIA. 199 @s278 mm. Ina very old male specimen of obesus from Alaska Giese measurements are respectively 220 mm. and 295 mm. In a somewhat younger but adult west Greenland specimen of rosmarus these dimensions are 195 mm. and 295 mm. Viewed anteriorly, the facial outline of the fossil specimens, especially in the oldest New Jersey example, shows affinity with the rosmurus type in the amelatively greater ratio of width to height, and in the Sable Island skull the median projection of the premaxillaries extends consider- ably beyond the anterior plane of the maxillaries into a blunt, beak- Ske process. [nm the very old recent Alaskan specimen the premaxillaries are -em a plane with the maxillaries at this point, and their median su- were recedes behind them at its antero-inferior border in a sort of baretip conformation. The three fossil specimens are remarkable for the great relative sme of the nasal bones. The New Jersey specimen now belonging te the Geological Survey of that State is much wider across the meaxillaries than the widest recent or fossil] walrus skull in the cus- ‘Gady of the Academy, and is from a very old individual. While we would expect a corresponding width of the nasal bones, these ame, wevertheless, correspondingly long, also, presenting an area mearly twice as great as in the largest recent walrus skulls in the -eatiection. The smaller New Jersey specimen, belonging to the Aeademy, also has a correspondingly large nasal area. The nasal gatures in the process of fossilization become sufficiently well-defined, even in the oldest specimens, to determine their area. In the larger Mew Jersey specimen the greatest nasal length is 98 mm., and the greatest width 80 mm. In thesmaller one these dimensions are 96 omm.and 81 mm. In the largest Greenland specimen they are 72 arm. and 65 mm., and in the largest Alaskan specimen 72 mm. and GE am. Turning now to the upper maxillary dentition, a comparison be- ‘Gweea the fossil and recent specimens of aged individuals shows the failowing marked differences in the permanent teeth.’ Em recent rosmarus of nearly the same size as the smaller New Sersey fossil specimen and 25 mm. shorter in basilar length than the Mewa Scotia fossil, all the grinding teeth average about one-half te dimensions of the fossil specimens, and making allowance for *K ade; the dental formula of Dr. Allen's Monograph of the Pinnipeds, wer 57. 200 PROCEEDINGS OF THE ACADEMY OF [1898. the difference in age they are more than one-third smaller. In the fossil specimens the permanent incisor exceeds the grinders both in triturating area and in alveolar depth and calibre. In rosmarus and obesus this tooth is much smallerthan ™*. The posterior molar (™*) in the fossil skulls (excepting the one belonging to the New Jersey Geological Survey),’ is a deeply rooted tooth of nearly the same calibre and triturating area as ™*. In both rosmarus and obesus it is the smallest and shallowest rooted of the permanent “_ tition and is sometimes wanting in aged specimens. Another marked character which is peculiar to the two fossil specimens belonging to the collection of the Academy, and in some degree to the specimen of the Geological Survey, is the remarkable median depression of the maxille at the incisive foramina, and the constriction of the inter-incisor space. In the Sable Island example the depth of the incisive foramina below the crown of ™? is 64 mm, and the distance between the alveoli of the permanent incisors is only 17 mm. In the Long Branch skull it is about the same. In the recent Greenland specimen these measurements are 41 mm. and 30 mm., and in the Alaskan specimen 50 mm. and 30 mm. While the foregoing comparisons were made with an amount of material far more comprehensive than that accessible td Dr. Leidy, and supplemented by the valuable diagnoses, figures and tables of measurements given by Dr. J. A. Allen, the author regrets that: a larger series of adult crania of our living species of walrus was not available. Premising, however, that the recent skulls used in this comparison are typical in essential characters of rosmarus and obesus, and that the fossil skulls, including the type of virginianus, all represent a period of Pleistocene Age, the writer concludes that the weight of evidence favors the separation of the fossil and recent species of Atlantic walrus under the following diagnoses: Rosmarus rosmarus (Linnus). Recent Atlantic Walrus. Phoca rosmarus Linneus ; Syst. Nat., 1758, p. 38. Rosmarus rosmarus Rhoads; Amer. Nat., 1894, p. 523. Characters.—Ratio of greatest anterior maxillary width to the paroccipital expansion, as 2 to 3; permanent upper incisor much smaller than ™?; ™* smallest, shallow-rooted, in old adults some times absent; superior grinders relatively weak, the opposing rows. rea by a wide incisive diastema twice the width of the largest 7In this the posterior molars have fallen out, the alveoli showing them to. have been of large calibre but quite shallow. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 201 molar; roof of mouth gently, evenly rounded, shallow between the grinders; incisive foramina small, not indented, their distance be- low the alveolus of "1 only equalling the distance between the two opposing permanent incisors; nasals small, short, rectangular. Rosmarus virginianus (DeKay). Fossil Atlantie Walrus. Satta virginianus DeKay ; Nat. Hist. N. York, I, p. 56, pl.19, fig. 1, a, b. Characters.—Ratio of greatest anterior maxillary width to par- occipital expansion, as 2 to 2}; permanent upper incisor as large as m?, ™% larger than ™!, nearly as large as permanent incisor, deeply rooted, persistent ; superior grinders massive, crowded, the opposing rows separated by a narrow incisive diastema about as wide as the largest molar: root of mouth deeply furrowed between the grinders ; incisive foramina large, acutely indented; their depth below the alveolus of ™! being twice as great as the space between the two opposing permanent incisors; nasals large, relatively long, becom- ing much wider anteriorly. It should be understood that the above diagnosis of the fossil wal- rus rests chiefly on the Sable Island specimen, and the finer skull belonging to the Academy from New Jersey which Leidy figured on plates 4 and 5 of volume XI of ‘the Philosophical Transactions. Both these skulls evidently belonged to very old males. In some respects, as in the relative sizes of the teeth to each other, the other New Jersey specimen and the plate of DeKay’s virginianus agree im their closer approach to the existing walrus. Owing to their frag- mentary condition, as compared with the Sable Island and Long Branch specimen, and the fact that the latter two agree exactly in all the characters enumerated, it is best to consider these as typical of the fossil animal. As DeKay’s type is destroyed and his diagno- sis and plate of little value, I would recommend that if the charac- ters pointed out in this paper as distinguishing the fossil from the recent Atlantic walrus are sufficiently confirmed by other speci- mens to warrant their separation, that DeKay’s name be retained. The evidence in favor of DeKay’s fossil being the same as roemarus and the other fossil specimens a distinct species, to which the name virginianus cannot apply, is too flimsy to merit attention. 14 202 PROCEEDINGS OF THE ACADEMY OF [1898. APRIL 5, The President, Samuret G. Drxon, M. D., in the Chair. Seventeen persons present. The death of Oliver A. Judson, M. D., a member, was announced. APRIL 12. The President, SAamMuEL G. Dixon, M. D., in the Chair. Twenty-six persons present. Pror. Prmspry made a communication on the natural history of slugs. (No abstract.) APRIL 19. The President, SamurEL G. Drxon, M. D., in the Chair. Nineteen persons present. The Function of the Radula—Mr. H. A. Pivspry spoke of a radula of the gastropod Nerita peloronta exhibited by Mr. Keely, mentioning its great length compared to that of the animal, and the large number of similar teeth at the margins. The modifications found by Fischer in the radula of Neritopsis and by the speaker in that of Orthomesus and the Helicide indicate that specialization in the Rhipidoglossa and Pulmonata has proceded from the median line of the radula outward, the outer teeth being the last to be modified, and therefore of value as indicating the ancestral con- dition; this mode of modification being probably the result of the greater functional activity of the median portion in feeding, due to the rounded shape of the subradular cartilage. Mr. CAuvert stated that the position of the radula in squids recently dissected by him seemed to preclude the use of that organ as a rasp, as described for snails. Mr. Pitspry replied that he had not observed any cephalopod feeding, but supposed that the radula here acted as an aid to deglutition, crowding the fragments, taken in the beak, down the cesophagus. Dr. CuAapMAN observed that he had often observed squids eating fish, and the beaks alone were used to bite the prey. He further alluded to the impossibility of keeping squids in aquaria owing to their incessant activity. They constantly dart against the glass and soon die from the mutilation ensuing. ———_ aS OOo 1898.] NATURAL SCIENCES OF PHILADELPHIA. 203 APRIL 26. The President, SamuEeL G. Drxon, M. D., in the Chair. Twenty-six persons present. A paper entitled “Materials toward a Natural Classification of the Cylindrelloid Snails,” by Henry A. Pilsbry and E. G. Vanatta, was presented for publication. Rock Inseriptions in Kauai, Hawaiian Islands—Dr. Bensa- MIN SHARP exhibited a specimen of coquina received from Mr. J. K. Farley of Kauai. He had visited Mr. Farley in 1893 with the hope of seeing some rock inscriptions usually covered with sand. An effort to uncover the rocks and expose the inscriptions had then been unsuccessful, although the bed rock had been reached at a depth of six feet. The following letter, accompanied by draw- ings of the inscriptions, has recently been received :— Ko.oa, Kauat, Hawarran Isuanps, July 18th, 1897. Dr. Benj. Sharp, Dear Srr:—When you were here in October, 1893, I promised you that 1 would send you any new information that I might obtain regarding the figures cut into the sandstone’ ledge at Keoneloa, also diagrams of them if I ever saw them again. On June 15th a native fisherman told me that the drawings were exposed to view at Jow tide. I went to Keoneloa June 16th, 17th, 18th, 19th and 21st, and send you herewith, in another package, the result of the visits. On the last date I could do nothing but try cutting the rock with a hatchet and an old native stone adze, as a high surf was fast covering the ledge again with sand. With a hatchet one could, I think, make a four foot figure in about two hours, steady work; with the adze it would take at least six times as long, and use up a number of such tools. Most of the figures look as if they had been cut with a semi-pointed implement like a rounded cold chisel. With the corner of the stone adze I was able to make about the same kind of a cut. A whirling motion that I noticed the waves as they ran off the rock gave to the sand, lodged it in the cuts and this may have worn the cutting into the sort of rounded pockets noticed. I had a talk, June 17th, with an old native woman named Kauila, who has lived near Keoneloa for many years. She said :— “T first saw the pictures when I was about thirteen years old (that was in 1848). I went to see them with my school-teacher and his other scholars and two Roman Catholic priests. My teacher's name was Alexandro, a Frenchman. He was the first Roman 1The rock is coquina, not sandstone. 204 PROCEEDINGS OF THE ACADEMY OF [1898. Catholic priest in Koloa and built the Roman Catholic Mission buildings. We saw a// the picture rocks exposed; you have only seen a part of them to-day. The priest went home with me from Keoneloa and talked with my father, Walewale, and with my grand- father, and also with a number of other old natives (in those days there were many old people in the land) about the drawings. They had all seen the pictures but had never heard who cut them, or why they were done. The oldest folks said that their fathers and grand- fathers had told them that the pictures had always been there.” The sand-hills to the west of Keoneloa are said to have been old battle-fields. They were certainly used as burial grounds as we know.’ Fugitives from the Oahu wars are said to have landed at Keone- loa and to have been killed and buried in these sand-hills by Koloa natives. Alexander, in his “ Brief History of the Hawaiian People,” Chap. 15, says “About the end of the 13th century, Kalaunuiohua, a war- like and ambitious Moi (King) of Hawaii, undertook to subdue the whole group ... he defeated the leading chiefs of Maui, Molo- kai and Oahu. ... he set sail for Kauai ... and landed near Koloa, where he was met by Kukona, at the head of the warriors of Kauai, and was totally defeated, his fleet being taken, his army de- stroyed. It was about this time that a vessel called ‘Mamala’ in the tradition, arrived at Kahului, in Maui. The captain and crew are said to have been foreigners of light complexion, with bright eyes, who intermarried with the natives and became progenitors of a light colored stock. As there were no Europeans in the Pacific Ocean in the 13th century, it is most probable, as Judge Fornander has suggested, that these foreigners were the crew of some Japanese junk, driven out of its course by a typhoon, and drifted to these shores, as has twice happened in recent times. Also, about the year 1527-28, Spaniards, a man and his sister, were saved from a wreck on Hawaii . . . they intermarried with the natives and became the progenitors of certain well-known families of chiefs, such as that of Kaikeowa, former Governor of Kauai.” Jarvis, in his history of the islands, says, “ Cook found in the possession of the natives of Kauai two pieces of iron, one a portion of a hoop, and the other appeared to be part of the blade of a broad- sword.” “The knowledge and use of iron was generally known.” Kauila’s story would take us back to the early part of the 17th century, without a tradition of the workers. The cross and the flag (?)* make me think that foreigners may have had a hand in the work, or may have given the natives, if they did the work, a knowledge of those emblems. Were it not for them one might think that the pictures were done by a party of ? We obtained, when with Mr. Farley, a number of bones and one complete skeleton. ’ Referring to the drawing sent with the letter. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 205 North-west Indians, who could, I believe, easily, in their large canoes, sail or drift down to the islands with the currents, in a shorter time than a Japanese junk could. One can usually see half a dozen N. W. drift logs on the beach at Keoneloa. On the beaches of Niihau, some fifty miles away, hundreds of logs and Red Wood posts have been picked up a few months after freshets on the Pacific coast of the U. S. and B. C., had washed out the logging dams of the saw mills. The last figure on my diagram, I take it, was made to represent a woman in parturition. P.S. Since writing the foregoing, I have seen Dr. Emerson of this place. He tells me that eight or nine years ago, he saw on the beach at Honaunau, Kona, Hawaii, somewhat similar drawings, cut into lava rock. Honaunau is not far from Keei, the place at which the Spanish man and woman are said to have landed in about 1527-28. The natives of Hawaii know nothing of the workers. Dr. Emerson says: Kackeoewa came from a Hawaiian family. My “cross” may be a totem. Mr. Wm. W. Jefferis was appointed Curator of the William S. Vaux Collections for the current year. The following were appointed the Committee on the Hayden Memorial Award for 1898:—Messrs Persifor Frazer, Angelo Heilprin, Theodore D. Rand, Benjamin Smith Lyman, and Jos. P. Lesley. The following were ordered to be printed :— 206 PROCEEDINGS OF THE ACADEMY OF [1898. BIRDS OBSERVED IN CENTRAL CALIFORNIA IN THE SUMMER OF 1898. BY JOHN VANDENBURGH. it was my good fortune in the summer of 1893 to be one of a party of five who, during the weeks from June 21st to July 27th, fairly lived in the saddle, riding nearly eight hundred miles through the Coast Range, interior valleys and Sierra Nevada of California. The other members of the party were Dr. Charles H. Gilbert, Dr. W. W. Thoburn and Professor C. B. Wing of Leland Stanford Junior University, and the Rev. Mr. Briggs, then of San Francisco. The main object of the expedition was the gathering of material which would throw light upon certain problems connected with the fish fauna of the streams in the vicinity of Mt. Whitney, but all forms of vertebrate life received more or less attention. My time was devoted chiefly to the birds and reptiles, the latter, perhaps, receiving the major share. Owing to the rapid rate at which it was necessary to travel, opportunities for collecting were not of the best, but the ornithological observations made, are presented in the hope © that they may be of interest from the fact that most of the birds were in their breeding ranges and, in many instances, in localities seldom visited by the ornithologist. Our route lay in Santa Clara County from Los Gatos and Palo Alto to Saratoga, and thence to Boulder Creek in Santa Cruz County ; June 21st, Santa Cruz; June 22d, Soquel, Aptos and Wat- sonville; June 23d, San Juan, Hollister and Tres Pinos; June 24th, up the valley of the San Benito River to San Benito, Hernandez, Hepsadan Mountain and Erie; June 26-29, across a divide to the Los Gatos Creek, June 29th, and then down this stream and through Pleasant Valley to Huron, June 30th. From: Huron we crossed the San Joaquin Valley, by way of Lemoore, Armona and Hanford, to Visalia, July 1-3d. From Visalia we went to Three Rivers and then up the east fork of the Kaweak River to Cain’s Flat, Weishar Mill and Mineral King, July 4-6th. Crossing Farewell Gap, we spent a day in Shotgun Cajion close to Little Kern River, and then went on to Trout Meadows and the south fork of Kern River, reach- ing Little Kern River Lake July 12th and Soda Springs or Big 1898.] NATURAL SCIENCES OF PHILADELPHIA. 207 Kern River Lake one day later. Our trail then lead us up Whitney Creek to its headwaters, across to Cottonwood Creek and thus down to Owen’s Lake and Lone Pine, July 14-16th. From Lone Pine we returned to San Francisco by way of Independence (July 17th), Big Pine (July 18th), Round Valley (July 19th), McGee’s (July 20th), Troy’s near Mono Lake (July 21st), Mono Pass and Dana Creek (July 22d), Yosemite Valley (July 23d), Crocker’s (July 24th), Buena Vista (July 25th), and Stockton (July 26th). 1. Colymbus nigricollis californicus. Eared Grebe. The Eared Grebe was seen only in Owen’s Valley, where a single pair were feeding in a small lake near Lone Pine, July 16, 1893. 2. Podilymbus podiceps. Pied-billed Grebe. A pair of this species inhabited a pond near Watsonville, where we camped, June 23d. 3. Ardea herodias. (reat Blue Heron. This heron was observed at Watsonville, June 23d. It was com- mon along the San Benito River, June 29th, and several were hunt- ing in the alfalfa fields of Pleasant Valley, June 30th. 4. Ardea virescens. (ireen Heron. The Green Heron was not uncommon along the San Benito River from Tres Pinos to San Benito, June 24-27th. One was observed on the east fork of the Kaweah River, July 5th. 5. Fulica americana. American Coot. Two Coots were playing in Little Kern River Lake early in the morning of July 15th. In Owen’s Valley a number were seen on a small lake near Lone Pine, July 16th. 6. Actitis macularia. Spotted Sandpiper. This loud voiced wader was seen at Kern River Lake, July 13th and 14th. 7. ZEgialitis vocifera. Killdeer. The Killdeer was observed near Watsonville, June 24th; at Tres Pinos, where it was very abundant along the San Benito Creek, June 25th, and along the Los Gatos Creek and in Pleasant Valley, June 30th. In the San Joaquin Valley, this bird was the almost constant accompaniment of water, July 1-4th. In Owen's Valley, many were seen along the streams and irrigation ditches between Lone Pine and Bishop, July 16-19th. 208 PROCEEDINGS OF THE ACADEMY OF [1898. 8. Oreortyx pictus plumiferus. Plumed Partridge. A large covey was observed near Mineral King, July 7th. Sev- eral were seen near Shotgun Cafion, July 11th, and a pair with half grown young were flushed between Trout Meadows and Kern River Lakes, July 12th. A single adult male was seen at Crock- er’s, July 25th. 9. Callipepla californica. California Quail. This quail was heard constantly between Saratoga and Boulder, June 21st. 10. Callipepla californica vallicola. Valley Quail. Valley Quail were very abundant along the east fork of the Kaweak River, July 4-5th, | 11. Dendragapus obscurus fuliginosus. Sooty Grouse. The Sooty Grouse was well represented at an altitude of about 8,000 feet near Mineral King. Here they were heard at all times of the day, and a female was seen with her covey of young, then about the size of Valley Quail, July 7th. Several were observed by Dr. Gilbert at the head of Shotgun Cajion, July 10th. 12. Zenaidura macroura. Mourning Dove. This species was first observed at Watsonville, where it was com- mon in the grain fields. After leaving Watsonville, it was with us constantly to San Juan, Hollister, Tres Pinos, up the valley of San Benito Creek, across into that of the Los Gatos, thence down Pleas- ant Valley to Huron, across the San Joaquin Valley to Visalia, and up the east fork of the Kaweak River to Cain’s Flat, at the lower limit of pines, June 24th, July 5th. Doves were very abund- ant in Owen’s Valley, from Lone Pine to Bishop, July 16th—-19th. 18. Pseudogryphus californianus. California Vulture. A single individual of this species was seen sitting on a fence- post near the road between Big Pine and Bishop Creek in Owen’s Valley, July 19th. 14. Cathartes aura. Turkey Vulture. ‘Buzzards were noted at Aptos, Watsonville, San Juan, Hollister, Tres Pinos, San Benito, Hernandez, Visalia, Three Rivers and Cain’s Flat. East of the Sierra Nevada several were seen in Owen’s Valley, and a dead one was found in Long Valley. 15. Circus hudsonius. Marsh Hawk. A hawk of this species was seen near Big Pine, Owen’s Valley, July 19th. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 209 16. Accipiter velox. Sharp-shinned Hawk (?). A bird thought to be of this species was seen near San Benito, June 27th. 17. Buteo borealis calurus. Western Red-tailed Hawk. Several Western Red-tails were sailing high in the air near Aptos, June 23d. The species was next seen at Tres Pinos, June 26th, but was not again observed until the party reached Dana Creek, above the Yosemite Valley, where one was shot July 23d. 18. Aquila chrysaetos. Golden Eagle. The only eagle seen flew from the ground near an irrigation ditch to a large oak, near Visalia, July 3d. 19. Falco sparverius deserticolus. Desert Sparrow Hawk, This species was first met at Soquel, where a single individual was seen June 23d. Others were observed near San Juan and Tres Pinos, June 24th. On June 27th one was seen near San Benito, feeding four young which had recently left the nest. 20. Glaucidum gnoma californicum. California Pigmy Owl. A Pigmy Owl was brought to me at Boulder by some boys who had shot it as it flew about their camp among the redwoods at noon June 22d. 21. Speotyto cunicularia hypogea. Burrowing Owl. A number of Burrowing Owls were seen near San Juan, June 24th. In Pleasant Valley and between there and Huron this spe- cies was very common, and often whole families of them could be seen on or near the mounds which contained their nesting burrows. June 30th, several were seen at various points in the San Joaquin Valley. 22. Geococcyx californianus. Road-runner. A Road-runner shot by Dr. Thoburn near Big Pine, July 18th, was the only one observed. 23. Ceryle alcyon. Belted Kingfisher. One Kingfisher was seen near Tres Pinos, June 26th. 24. Dryobates pubescens gairdnerii. Gairdner’s Woodpecker. This Woodpecker was very abundant along the San Benito Creek, June 25th to 28th. 25. Dryobates nuttallii. Nuttall’s Woodpecker. Nuttall’s Woodpecker was observed only on the east fork of the Kaweah River near Cain’s Flat, July 5th. 210 PROCEEDINGS OF THE ACADEMY OF [1898. 26. Xenopicus albolarvatus. White-headed Woodpecker. The White-headed Woodpecker was very common among the pines between Weishar Mill and Mineral King, July 7th. 27. Sphyrapicus ruber. Red-breasted Sapsucker. Several “ Red-headed Woodpeckers” were busy in the pines at Kern River Lakes, July 13th. 28. Sphyrapicus thyroideus. Williamson’s Sapsucker. This bird was quite common among the pines and sequoias near Weishar Mill, July 7th. Several were seen near Kern River Lakes, July 12th to 14th. 29. Ceophleus pileatus. Pileated Woodpecker. A bird of this species was noted at Weishar Mill, July 6th. 30. Melanerpes formicivorus bairdi. California Woodpecker. This showy bird was usually seen in flocks of from three to a dozen individuals. It was noted among the redwoods at Boulder, June 21st, and in the oaks near Watsonville, San Juan, Tres Pinos and San Benito, June 23d to 27th. In the San Joaquin Valley it was common—particularly so near Visalia, July 3d—but ascended the east fork of the Kaweah only to Cain’s Flat. 81. Melanerpes torquatus. Lewis’ Woodpecker. Many Lewis’ Woodpeckers were circling in the air along San Benito Creek between Tres Pinos and Hepsadan Mt., June 25th— 29th. 32. Colaptes cafer. Red-shafted Flicker. A Flicker was noted at Watsonville, June 23d; another was seen near San Juan, June 24th, and several were observed in San Benito Valley, June 27th-29th. In the high Sierras three were seen in Shotgun Cajion, July 10th. 33. Phalaenoptilus nuttallii californicus. California Poorwill. Several Poorwills were heard in the foot hills near Tres Pinos throughout the moonlit night of June 25th. 34. Chordeiles virginianus henryi? Western Night Hawk. While all Night Hawks seen were flying so high as to prevent their capture, it seems probable that two, seen near Tres Pinos, June 25th, and also several observed at Kern River Lakes, July 13th, were of this form. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 211 35. Chordeiles texensis ? Texan Night Hawk. A number of Night Hawks seen at Big Pine, Owen’s Valley, July 18th, were referred to this species. 36. Chetura vauxii. Vaux’s Swift. Five Vaux’s Swifts were seen with a flock of Violet-green Swal- lows near Boulder, June 21st. It is probable that they were breed- ingin hollow redwoods. 37. Trochilus alexandri, Black-chinned Humming-bird. This Humming-bird was noted only near Lone Pine, where sey- eral were observed July 16th. 88. Calypte anna. Anna’s Humming-bird. Near Watsonville this fine bird frequented the blossoms of the buckeye, June 24th. Several were seen near San Benito, June 26th-27th. 39. Selasphorus rufus. Rufous Humming-bird. Two individuals of this little species were observed near Mineral King, July 7th. They were flying about a clump of low bushes at an altitude of about 7,500 feet. 40. Tyrannus verticalis. Arkansas Kingbird. The western Kingbird was very common in the vicinity of San Juan, Hollister and Tres Pinos, June 25th. At Tres Pinos a pair had a nest which contained four young nearly ready to fly. The species was observed in the valley of the San Benito as far up as Erie. In the San Joaquin Valley this bird was very abundant, and several nests had been built upon the crossbars of telegraph poles. It was noted near the east fork of the Kaweah, but disappeared a short distance above Cain’s Flat, July 6th. In Owen’s Valley several were noted near Lone Pine and Inde- pendence, July 16th-17th. 41. Myiarchus cinerascens, Ash-throated Flycatcher. The Ash-throat was quite common in the Coast Range between Saratoga and Boulder, June 21st. It was observed in the hills near Watsonville, June 23d, and at the headwaters of the San Benito Creek, June 29th. 42. Sayornis saya. Say’s Phoebe. A pair of Say’s Phoebes had a nest in a barn in Round Valley, which contained two large young, July 19th. 212 PROCEEDINGS OF THE ACADEMY OF [1898. 43. Sayornis nigricans. Black Phoebe. The Black Phoebe was not uncommon at Boulder, June 2\1st, Watsonville, San Juan and Hollister, June 24th, Tres Pinos June 25th, and San Benito, June 27th. Several were observed along the east fork of the Kaweah, July 4th. 44. Contopus richardsonii. Western Wood Pewee. The Western Wood Pewee was common along the streams near Saratoga and Congress Springs, June 21st, but was not again met except on the east fork of the Kaweah River, where several were observed July 5th. 45. Pica nuttallii. Yellow-billed Magpie. The Yellow-billed Magpie was common at Visalia, July 3d. . 46. Cyanocitta stelleri frontalis. Blue-fronted Jay. This Jay was very common in the Coast Range between Saratoga and Boulder, June 21st. It was again noted shortly after entering the coniferous woods on the east fork of the Kaweah, July 6th; was very common at Weishar Mill, and ranged up almost to Min- eral King, July 7th. 47. Aphelocoma californica. California Jay. The California Jay was found in the Coast Range between Sara- toga and Boulder, June 21st. It was common along the San Benito Creek from Tres Pinos to its source, June 15th-29th, and was again observed at Visalia and along the east fork of the Ka- weah to the lower limit of pines. 48. Corvusamericanus. Crow. Crows were abundant near San Benito, June 27th, and several small flocks were seen in Pleasant Valley, June 30th. They were very numerous between Visalia and Three Rivers, July 3d. 49. Nucifraga columbiana. Clark’s Nutcracker, A noisy troop of Clark’s Crows was observed almost at the top of Farewell Gap, July 8th. The species was again seen near the head waters of the south fork of the Kern River, July 15th. 50. Agelaius pheniceus. Red-winged Blackbird. Red-wings were many near Watsonville, June 24th. A few were seen at Trout Meadows, July 12th, and several near Lone Pine, July 17th. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 213 51. Sturnella magna neglecta. Western Meadow Lark. This Meadow Lark was abundant in the fields near Watsonville, San Juan, Hollister and Tres Pinos, June 23d to 26th, and in al- most all parts of the San Joaquin Valley where any low vegetation grew July Ist to 4th. 52. Icterus bullocki. Bullock’s Oriole. Bullock’s Oriole was observed near the following places: San Juan and Hollister, June 24th; Tres Pinos, where a pair had a nest which contained large young, June 25th; San Benito, June 27th; Erie, June 29th; Los Gatos Creek, June 30th; Lemoore, July 1st; Visalia, July 4th; east fork of the Kaweah River, July 5th ; and Yosemite Valley, July 24th. 53. Scolecophagus cyanocephalus. Brewer’s Blackbird. Brewer’s Blackbird was noted near the following places: Sara- toga, June 21st; Watsonville, June 23d; San Juan, June 24th; Hollister, June 24th; Tres Pinos, June 26th; San Benito, June 27th ; Lemoore, July 1st ; and Trout Meadows, July 12th. 54. Carpodacus purpureus californicus. California Purple Finch. The California Purple Finch was not uncommon in the Coast Range near Boulder, June 21st. Three were seen near Watson- ville, June 23d. 55. Carpodacus cassini. Cassin’s Purple Finch. Cassin’s Finch was first seen a mile or two below Mineral King, on the east fork of the Kaweah, July 7th. They were much more numerous in Shotgun Cajon, July 8th to 10th. 56. Carpodacus mexicanus frontalis. House Finch. The “ Redhead” was found near Watsonville, San Juan, and Hollister, June 24. It was plentifully distributed in San Benito Valley from Tres Pinos up to the divide. A pair had a nest in a tin can hung in the porch of a farm house on the east fork of the Kaweah River, which contained two young birds, July 4th. 57. Leucosticte tephrocotis.. Gray-crowned Leucosticte. Farewell Gap was filled with snow on July 8th, and here several small flocks of Gray-crowned Finches were busily feeding on smal] flies and grubs. A single bird of this species was seen in Mono Pass, July 22d. 58. Spinus tristis. American Goldfinch. The American Goldfinch was observed only near Watsonville, June 23. It is abundant near Monterey in May and June, where 214 PROCEEDINGS OF THE ACADEMY OF [1898. it is associated with S. psaltria, S. lawrencei, 8S. pinus, Carpodacus purpureus californicus and C. mexicanus frontalis. 59. Spinus psaltria. Green-backed Goldfinch. “ Wild Canaries” were many between Santa Cruz and San Ben- ito, June 22d to 27th. Others were noted at the headwaters of the San Benito Creek, June 29th. 60. Spinus lawrencei. Lawrence’s Goldfinch. Several Lawrence’s Goldfinches were seen near San Benito, June 26th. The species was not observed elsewhere. 61. Chondestes grammacus strigatus. Western Lark Finch. The “ Field Sparrow ” was very common in the grain fields near Watsonville, San Juan, Tres Pinos and San Benito, June 23d to 27th. It was seen also at Armona, in the San Joaquin Valley, July 1st. 62. Zonotrichia leucophrys. White-crowned Sparrow. The White-crowned Sparrow breeds commonly near Weishar Mill and extends its range up the east fork of the Kaweah to an altitude of about 10,500 feet. Here several were heard singing where more than half the ground was covered with snow, July 8th. A nest, found near the source of Owen’s River, contained four young, apparently just hatched, July 21st. 63. Spizella socialis arizone. Western Chipping Sparrow. Chipping Sparrows were quite common in San Benito Valley, June 26th to 29th. 64. Junco hyemalis thurberi. Thurber’s Junco. Thurber’s Junco was everywhere throughout the timbered regions near Mineral King, July 7th, Shotgun Caiion, July 9th-11th, Kern River Lakes, July 13-14th, and Little Yosemite, July 23d. Near Weishar Mill a nest was found which contained three small, young, July 7th, while one near Kern River Lakes contained four nearly fresh eggs, July 14th. 65. Junco hyemalis pinosus. Point Pinos Junco. This Junco, described from Monterey, was found breeding abund- antly in the Coast Range from the vicinity of Saratoga to Boulder, June 21st. At Boulder it was even more common than at Monterey in May. 66. Amphispiza belli nevadensis. Sage Sparrow. Several birds of this species were shot near Big Pine, Owen’s Valley, July 18th. 1898.] © NATURAL SCIENCES OF PHILADELPHIA. 215 67. Melospiza fasciata samuelis. Samuel’s Song Sparrow. This bird was common near Saratoga, June 21st. 68. Melospiza fasciata heermanni. Heermann’s Song Sparrow. A few were found at Lone Pine, July 17th. 69. Passerella iliaca megarhyncha. Thick-billed Sparrow. The Thick-billed Sparrow was observed only between Shotgun Cafion and Trout Meadows, July 11th. 70. Pipilo maculatus oregonus. Oregon Towhee. This species was constantly present in the Coast Range between Saratoga and Boulder. Many of the specimens approach P. m. meg- alonyz. 71. Pipilo fuscus crissalis. Californian Towhee. The California Towhee was rarely out of sight between Saratoga and Santa Cruz, June 21st-22d. Several were seen near Watson- ville, June 23d, Hollister, June 24th, San Benito, June 26th, and Erie, June 29th. 72. Habia melanocephala. Black-headed Grosbeak. This Grosbeak enlivened the woods between Saratoga and Boul- der, June 21st. It was again observed at Aptos, June 23d, and was abundant in San Benito Valley, June 25th-29th. One was seen in Yosemite Valley, July 24th. 73. Guiraca c#ruiea eurhyncha. Western Blue Grosbeak. The Western Blue Grosbeak was first observed near Lemoore in the San Joaquin Valley, July 1st. In Owen’s Valley it was com- mon near Independence, July 18th. 74. Passerina amena. Lazuli Bunting. The Lazuli Buntings were singing along the road between Sara- toga and Boulder, June 21st. Several were observed near Watson- ville, June 24th, between San Juan and Hollister, June 24th, and in San Benito Valley, June 26th-29th. In Owen’s Valley the species was seen a number of times near Lone Pine, July 16th-17th. One was found in Yosemite Valley, July 24th. 75. Piranga ludoviciana. Western Tanager. The Western Tanager was observed on the east fork of the Kaweah River from Cain’s Flat to near Mineral King, July 6th- 7th. It was common in Shotgun Cafion, July 9th-11th. 216 PROCEEDINGS OF THE ACADEMY OF [1898. 76. Petrochelidon lunifrons. Cliff Swallow. Cliff Swallows were plentiful in the region around Soquel, Aptos, Watsonville, San Juan, Hollister, Tres Pinos, San Benito and Erie, June 23d-29th. A colony had about a hundred nests fastened to the side of a cliffnear San Benito, Ten of these nests were exam- ined June 26th. One held three fresh eggs, two each contained three adult birds, the others were empty. In Owen’s Valley this species was very abundant at Lone Pine, July 17th, at Independence, July 18th, at Big Pine, July 19th, and near Bishop, July 20th. 77. Chelidon erythrogaster. Barn Swallow, The Barn Swallow was rare near Tres Pinos, June 26th. It was. not again met until Owen’s Valley was reached, where it was found associated with P. lunifrons at all points visited. Two young, which had just left the uest, were sitting on a rafter ina barn at Big Pine, July 18th. A nest near Bishop contained fresh eggs, July 19th. 78. Tachycineta thalassina. Violet-green Swallow. Several Violet-green Swallows were flying with the swifts at Boulder, June 21st, and a few were seen in San Benito Valley, June 26th-28th. 79. Phainopepla nitens. Phainopepla. A bird of this species was seen in the Valley of the Los Gatos Creek, June 30th. Several “ White-winged Blackbirds” were ob- served on the east fork of the Kaweah, a short distance above Three Rivers, July 4th. 80. Lanius ludovicianus gambeli. California Shrike. (7) A Shrike was seen at Watsonville, June 23d, and others at Hol- lister and Tres Pinos, June 24th. A number were in the lower part of San Benito Valley, June 26th-27th, and in the San Joaquin Valley near Huron and Armona, July Ist. 81. Vireo gilvus. Warbling Vireo. The Warbling Vireo was encountered only in San Benito Valley, where it was not uncommon, June 27th—28th. 82. Helminthophila celata lutescens. Lutescent Warbler. This warbler was singing everywhere in the Coast Range near Boulder, June 21st, but was not again observed until near Mineral King, where several were feeding at an altitude of 7,400 feet, July 7th. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 21 J 83. Dendroica aestiva. Yellow Warbler. Several Yellow Warblers were playing in the bushes near Sara- toga, June 21st. One was noted at Watsonville, June 23d, and the species was well represented in the San Benito Valley, June 26th— 28th. 84. Dendroica occidentalis. Hermit Warbler. A single male of this species was seen among the willows at Min- eral King, July 8th. 85. Clinclus mexicanus. Ousel. Two Ousels were flirting on a raft of logs under a bridge in the town of Boulder, June 22d. One was observed near Mineral King, July 7th, standing upon a rock in the middle of the east fork of the Kaweah River, which at this point is a mass of foaming rapids. Soon it started up the stream but quickly dived under the water to reappear a few moments later some distance below its starting point. This performance was repeated several times. An adult and two full grown young were secured on the Little Kern River at the foot. of Shotgun Cajion, July 10th. 86. Oroscoptes montanus, Sage Thrasher. The only Sage Thrasher observed was hanging with its neck pierced by a barb of a wire fence in Round Valley, July 19th. 87. Mimus polyglottos. Mockingbird. Mockingbirds were living in the gardens at Lemoore, July Ist. Several were heard near Visalia, July 3d. 88. Harporhynchus redivivus. California Thrasher. , The “ Mountain Mockingbird ” was numerous in the Coast Range between Saratoga and Boulder, June 21st. Several were observed in the foothills near Watsonville, June 23d. 89. Harporhynchus lecontei. LeConte’s Thrasher. One was noted between Independence and Big Pine, July 18th. 90. Thryothorus bewickii spilurus. Vigor’s Wren. This Wren was frequently heard in the Coast Range north of Boulder, June 21st. 91. Certhia familiaris occidentalis. California Creeper. Two Creepers were busily examining the trunk of a redwood near Boulder, June 22d. Several were seen at Weishar Mill (altitude 6,720 feet), July 7th. One was shot at Kern River Lakes, July 14th. 15 218 PROCEEDINGS OF THE ACADEMY OF [1898. 92. Parus inornatus. Plain Tit. This bird was seen only in the Coast Range north of Boulder, where it was generally distributed, June 21st. 93. Parus rufescens neglectus. California Chickadee. Troops of Chickadees scolded as I rode through the Coast Range between Saratoga and Boulder. One was seen near Watsonville, June 23d. 94. Chamea fasciata. Wren Tit. This little bird was rarely silent in the chaparral of the Coast Range north of Boulder, June 21st. Others heard near Watson- ville and San Benito were probably of this form. 95. Chamea fasciata henshawi. Pallid Wren Tit. Wren Tits, which were heard, but not obtained, at Cain’s Flat on the east fork of the Kaweah, July 5th, were doubtless of this pale race. 96. Psaltriparus minimus californicus. California Bush Tit. This Bush Tit was very abundant in the Coast Range near Boul- der, June 21st, and also near San Benito, June 27th-28th. Several flocks were seen near the east fork of the Kaweah a few miles above Three Rivers, July 4th. 97. Regulus satrapa olivaceus. Western Golden-crowned Kinglet. A Golden-crowned Kinglet flitted about in the pines near the trail between Shotgun Cafion and Trout Meadows, July 11th. 98. Turdus ustulatus. Russet-backed Thrush. This species was in full song near Boulder, June 21st. Several were noted near Aptos, June 23d. > 99. Merula migratoria propinqua. Western Robin. Robins were first met among the pines along the east fork of the Kaweah, at an altitude of about 6,000 feet, July 6th. They were common in Shotgun Cajon and at Trout Meadows, July 10th-11th. Several were observed at Kern River Lakes, July 12th-14th. 100. Sialia mexicana occidentalis. Western Bluebird. A few birds of this species were observed near Boulder, June 21st, one at Watsonville, June 23d, and others in San Benito Valley, June 26th-29th. 101. Sialia arctica. Mountain Bluebird. Mountain Bluebirds were often seen in Shotgun Cajion, July 10th, but were not observed elsewhere. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 219 REVISION OF THE NORTH AMERICAN SLUGS: BINNEYA, HEMPHILLIA, HESPERARION, PROPHYSAON AND ANADENULUS. BY HENRY A. PILSBRY AND E. G. VANATTA. In a former essay’ we undertook a revision of the Arionid genera Ariolimax and Aphallarion. In the present paper the remaining American genera of Arionide are similarly treated. Profiting by a criticism from one’ whom all limacologists acknowl- edge as master, we have extended our anatomical observations to the pallial organs, muscle system, ete., with interesting and we believe important results. The genera of Arionidee, often scattered even by the great malacol- ogists among Helicid or Limacid groups, now fall into orderly se- quence ; and in the flood of light disclosed by comparative study of the myology, the phylogeny and approximately final classification of the various groups is seen clearly outlined before us. Trivial and unsatisfactory as are the external features of slugs, the details of their internal morphology are wonderfully varied. Everywhere there are important characters; and those who starve their souls on a mere study of the genitalia and oral armature miss the best part of the feast. Believing with Cope that all the facts of morphology should be taken into account in systematic classification—that “ system ” is, in fact, an epitome of the total structure, as well as, with certain dis- tortions, a phylogeny of organisms, we have freely used characters from all organs in which we found differentiation, in the construe- tion of our scheme of family, subfamily and generic classification. We must again gratefully acknowledge our indebtedness to vari- ous friends and correspondents for material received, and especially to Messrs. P. B. Randolph, J. G. Malone and Fred. L. Button, Slugs have also been received from J. G. Cooper, 'l. D, A. Cockerell, E. H. Ashmun, Wm. H. Dall, W. G. Binney and others; and the series in our collection from Henry Hemphill has also been of great service. 'Proc. Acad. Nat. Sci. Phila., 1896, pp. 359-350, pl. xii-xiv. ? Dr. H. Simroth, in Zoologisches Centralblatt, [V, No. 6, March, 1897. 220 PROCEEDINGS OF THE ACADEMY OF [1898. Our observations may be grouped under four captions: I, Notes - on the comparative anatomy of Arionide ;* II, Classification ; III, Descriptions of the genera and species, and IV, Brief directions for collecting and preparing slugs. I, ANATOMY OF ARIONIDA. General external features—Slugs of the family Arionids vary in external form from the typical Limax shape, to forms with a con- spicuous dorsal hump. The mantle is generally oval, situated anter- iorly on the body, and completely closed over the shell, but in the humped forms it is more posterior and larger, extending some dis- tance in front of the shell, which is more or less exposed. The breathing pore is in its right side near the edge, connected therewith by a gutter. The mantle is adnate at the sides and behind, but free for some distance in front. The foot always has longitudinal “ pedal furrows ” above its lateral edges, defining a vertically grooved band or “foot margin.” The pedal furrows meet at the tail, at which point there is often a “caudal gland,” pit or slit developed. The surface sculpture of the integument of the foot is varied in the several genera and species. In Ariolimax there are close parallel grooves aboye, becoming oblique and more spaced at the sides, and with less conspicuous grooves at right angles to these, uniting them. In Hemphillia, Binneya and Anadenus there is a dorsal groove run- ning back from the mantle, with oblique grooves branching from it on each side. In Prophysaon the surface is divided into a reticula- tion of long diamond shaped meshes by pigmented grooves, each mesh being further subdivided. One species, P. caruleum, is an exception, having longitudinal grooves as in Ariolimaa or Arion. The sole is distinctly divided into three longitudinal tracts separ- ated by grooves in Anadenulus. In some other genera (Ariolima- cine) there is an indistinct tripartite division, while in others (Pro- physaon, Hemp hillia, ete.), this is not recognizable. Shell—The shell varies in form from a moderately well developed spiral (Binneya) or a convex plate (Hemphillia) exposed entirely or in part by an orifice in the mantle, to a nearly flat, wholly inter- nal plate as in most of the other genera. In some forms of Prophy- * The elementary character of a portion of this paper scarcely calls for apol- ogy in view of the fact that the study of slugs in America is still in an em- bryonic condition. While in Europe there are many expert observers, we have probably not more than four or five men in America who have given especial attention to them. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 221 saon and Arion this plate is largely cuticular, the calcareous layer being represented only by scattered, angular, granules. In all cases the shell-cavity in the mantle is small, not much larger than the en- closed shell. This contrasts strongly with the allied family Philo- mycide, which has an enormously extended, empty shell sack. General internal topography.—In most genera of completely limaciform external contour, the body from head to tail is excava- ted into one general body cavity (see these Proceedings for 1896, Pl. XIU, fig. 1), in which the digestive system lies extended, with the genitalia lying parallel with or across it, the liver or liver and ovo- testis extending into the tail. In genera with a dorsal hump (Bin- neya and Hemphillia) that portion of the foot behind the posterior end of the hump is not excavated, but solid as in Helix and other spiral-shelled genera. The liver and ovotestis lie in the posterior portion of the cavity of the hump, into which the viscera are crowded upward and forward. Along the floor of the body cavity, extending from below the mouth a variable distance backward, lies the suboral gland (P. A. N.S., 1896, Pl. XIII, f. 1), which in some genera is deeply imbedded in the muscular tissue of the sole, in others lies lightly attached thereto. In Ariolimax and its immedi- ate allies the genital system including the ovotestis, is crowded for- ward into the anterior half of the animal’s length; in Prophysaon and most other genera it lies stretched out at greater length, and the albumen gland and ovotestis are decidedly posterior. Other peculiarities in the arrangement of the organs are noticed below. Alimentary tract.—The buccal body in Arionide is short, as in allied families of snails. The jaw varies from thin and flexible to strong, is of the ordinary arched form, and is always sculptured an- teriorly. The usual sculpture consists of numerous flattened ribs denticulating the cutting margin; but in Prophysaon fasciatum: the structure is rather a series of narrow, hardly overlapping or imbri- cating plaits, much as in some species of the genus //ammulina of the Endodontide. In P. humile the plaits seem quite lost in a general, close, vertical striation, as in Pyramidu/a, also a genus of Endodontide. The radula resembles that of the Endodontide. The central teeth are tricuspid, ectocones small. Lateral] teeth bicuspid, passing *This gland, the function of which is to secrete mucus to lubricate the sole in crawling, was erroneously interpreted as a buccal retractor muscle by Binney, Man. Amer. Land Shells, p. 98, second paragraph from tup. 222 PROCEEDINGS OF THE ACADEMY OF [1898. gradually into the marginal series by shortening of the basal-plates. Marginals bicuspid, with occasionally a tooth with the ectocone bifid. In the Ariolimacine the inner cusps of the outer lateral and inner marginal teeth are much lengthened and oblique, the ectocones much reduced, simulating the pseudo-zonitoid teeth of Flammulina. Arion also shows this tendency to a much less degree. In the other genera the cusps of these teeth are short or of moderate length. All Arionide have four longitudinal folds of the intestine,’ as usual in slugs generally ; the main divergence being in the compar- ative length of the folds and the degree of their torsion. The folds are designated by the initial G with exponents 1, 2, 3, 4, as in PI. XI, fig. 29. The anterior loop between G’ and G° is caught up by the cephalic artery immediately upon its emergence from the di- aphragm (PI. XIV, figs. 66,70,72). In Arion the posterior loop between G! and G’, forming the lower end of the stomach, lies pos- terior to all other intestine folds;® but in all the other American genera the loop formed by G* and G* lies behind the stomach. In Ariolimax, Aphallarion and Hespearion (Pl. XI, fig. 33) the gut is long and spirally wound. In Prophysaon (Pl. XI, figs. 28— 30, 32, 34), Anadenulus (fig. 35), Hemphillia (fig. 36) and Binneya (fig. 31) it is much less twisted spirally. In the latter two genera the posterior loop formed by G* and G+ is very short, on account of the crowding forward of the viscera into the dorsal hump. In Prophysaon, Anadenulus, Hemphillia and Binneya there is no differentiation of the first fold into crop and stomach, such as occurs in Ariolimaa, ete. Reproductive organs.—In the Arionide there are two main types of genital organs. In the more primitive and normal type there is a well developed penis provided with a retractor muscle, and in every way homologous with the same organ in the Helices and pul- monate snails generally. This may be seen in Aviolimax, Hesper- arion (Pl. XII, figs. 44,47), Binneya, Hemphillia, and the Himal- ayan genus Anadenus. In the slugs, as well as in many other snails, the terminal portion of the vas deferens is noticeably enlarged, often considerably swollen for a distance above its insertion in the penis (see Pl. XII, fig. 49, epi., Hemphillia ; and these Proceedings, 1896, Pl. XIV, fig. 14, epi., Ariolimax). This enlarged tract has 5In Afhallarion there is a short loop interposed between the second and third long folds, making six folds. See P. A. N.S., 1896. pl. 18, f. 4. 6p. A. N.S., 1896, Pl. 13, f. 3. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 225 been called the “epiphallus.” In the other type, to which Arion, Geomalacus, Prophysaon and Aphallarion belong, the penis has been lost through degeneration, and the vas deferens enters the atrium directly, its lower course being enlarged or modified in various ways (Pl. XIII, all figs.) as described above, into an epiphallus.’ The epi- phallus is not evertible, has no retractor, and does not have the function of a penis. Init the sperm is lodged in packets or “ sperm- atophores.” These, in Hesperarion and Prophysaon, are oblong, narrow capsules of chitinous texture, with a long, slender filament at one end (PI. XII, fig. 43). They may occasionally be found in the spermatheca (Pl. XII, fig. 48, where the outlines of several are faintly visible through the wall). In genera with this type of geni- talia the vagina and lower portion of the free oviduct are introvert- ible, and assume the function of the penis, being provided with a retractor or retractors; and in some genera, such as Avion, the spermatheca duct also has a retractor muscle. In forms having the spermatheca duct inserted directly upon the atrium, there is, of course, no vagina, and the free lower portion of oviduct alone acts as penis... The peculiar enlargement of the epiphallus in Prophy- 7The term epiphallus was originally proposed some years ago by the senior author of this paper for the structure as commonly found in such Ae/icide as the West Indian Caraco/us and Pleurodon/e species, and in most of the larger Kast Indian and Australian forms, in which it occurs associated with a well- developed penis. as in Hesferarion, etc. It is strictly synonymous with Sim- roth’s term ‘‘Patronenstrecke.”’ Mr. Collinge (Proc. Zool Soc. Lond., 1897, p. 447) proposes to substitute ‘‘sperm-duct’’ for what we term epiphallus, and restrict the latter name to ‘‘ the terminal portion of the vas deferens above the sperm-duct.” There is, of course, no objection to the substitution of an English name for the Greek compound, but since the term epiphallus has already been used in extensive and numerous works in America, England and Germany, it seems a little revolutionary to completely alter its significance. If Mr. Collinge wants a term for the vas deferens above the epiphallus, he had better, to avoid confusion, invent a new one; though what he wants it for is not quite apparent * Arion is a case in point, ¢/, Collinge, Proc. Zool. Soc. Lond., 1897, p. 447. Geomalacus also is similar. In Prophysaon and Ap/allarion however, it is the vagina proper which performs both its usual function and that of an evertible penis. We consider Mr. Collinge’s statement (/. c.) that ‘‘ Messrs. Pilsbry and Vanatta have suggested the term * * * vagina for what I term free- oviduct’’ as an inadequate representation of our position, due, no donbt. to our inadvertent enumeration of Arion as one of the genera in which the vagina functions as a penis. We use the term “ vagina’ for the passage below the union of the spermatheca duct with the free oviduct proper (see Pl. XIII, fig. 57, vag.), considering such usage justified by its functions. The term “ free oviduct’ will naturally be retained for the passage from the apex of the va- gina (when present) to the point of approximation of the vas deferens. Mor- phologically, the vagina may be regarded as an elongated portion of the atrium. 224 PROCERDINGS OF THE ACADEMY OF [1898. saon is not hollow like a penis, but has a small duct only, the walls being solid and muscular. The remaining organs do not differ from their usual structure in Aulacopod pulmonates, although the position of the ovotestis is varied in the several genera. Muscles—Only the muscles lying free in the body cavity, not those composing the external walls or sole, will be considered herein, the latter being morphologically similar in Arionide to the other land snails. The free muscles belong to two groups: (1) retractors of the bue- cal mass, eye-peduncles and tentacles, and (2) retractors of the generative organs. The buccal and tentacle retractors, with the foot retractor or re- tractors in ordinary spiral-shelled snails converge and are attached posteriorly or proximally to the columella of the shell. In Limacid or Arionid slugs the degenerate shell no longer serves as a support for these muscles, which are inserted at or near the posterior margin of the diaphragm, or floor of the lung; this position approximating pretty closely to the posterior or former columellar margin of the vestigial shell. In the more primitive genera, Binneya, Hemphillia, Ariolimaz, ete., the retractors still converge to a point near the middle of the back margin of the lung, under the posterior edge of the shell (Pl. XIV, figs. 65, 66, 67, 69, 71). In the more divergent genera Arion (PI. XIV, fig. 72) and Prophysaon (PI. XIV, fig. 70), the eye and tentacle retractors have moved from the middle to the outer posterior angles of the diaphragm. The convergent retractors of Ariolimaz and its allies are a heritage from the spiral-shelled an- cestors of the family, although the utility of the convergence is no longer present; while the parallel retractors of Arion, ete., are a later modification which resulted in a straight backward pull of each retractor, independent of the others, and possibly brought about mechanically by the tendency toward separation of the grouped proximal insertions by strains on the converging muscles from their separated distal terminations. Another muscle more or less closely associated with the buccal and tentacle retractor system, is found in Ariolimax, Hemplhillia and allied genera (PI. XTV, figs. 65, 66, 69). This is a band passing from near the proximal insertions of buccal and eye retractors forward across the diaphragm to an insertion in the top or right side of the head. It has been termed the “ reten- sor” by Simroth, who observed it in Ariolimax Californicus, and — 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 225 supposed it to be an aid to the extension of the penis. We scarcely endorse this view of its function, after observing it in several other genera in which it is not inserted near the atrium, but in the integ- ument of the head or back above. It may aid in withdrawing the head beneath the mantle. Morphologically this muscle is regarded by Simroth asa slip detached from the body-wall. In this, again, we are compelled to dissent. We regard it as a retractor pedis, the anterior insertion of which has moved from the sole to the side or upperintegument. Pending further investigation into its physiolo- gic function and morphologic equivalency, we continue to use Sim- roth’s name “ retensor” for this muscle. The retractors of the genitalia are far less constant in form, num- ber and position than those of the buccal mass and eyes. ‘Their proximal insertions here, as in the spiral snails, are on the diaphragm or lung floor. The chief muscles of this system are the penis retrac- tor (PI. XIV, figs. 66,71 r.p.), which is almost invariably inserted ou the left side of the diaphragm, and the oviduct retractors (PI. XIV, fig. 67, vag. r.), which may be inserted either upon the diaphragm or at its posterior border. The latter are well developed only in those genera in which the oviduct or vagina has assumed the function of a penis. In Arion and Geomalacus the spermatheca duct also has a retractor. The several retractors of the female or- gans are quite inconstant in position and number (being often in- creased by splitting). They are not homologous with the penis re- tractor, but have been developed de novo in the genera requiring them. Another muscle deserving mention is a short band uniting the swollen epiphallus to its peduncle, in the genus Prophysaon (PI. XIU, fig. 57, muse.). ‘This muscle.so conceals the true structure of base of the epiphallus that no former authors with the exception of Simroth, have correctly described or represented it. Pallial region — Underlying’ the retractor muscle system is seen a thin but dense membrane perforated only by the aorta and the rectum. ‘This is the “diaphragm” separating the body cavity from that of the lung (indicated in outline in the figures on Pl. XV). Removing the diaphragm, the inner surface of the lung is exposed, densely reticulated with blood vessels (P|. XV, fig. 73). The breath- ing pore or pulmonary aperture (PI. XV, fig. 77, p. a.) is situated at *The slug being pinned back downward in the dissecting pan. In the natural position of the animal it overlies the muscles. 226 PROCEEDINGS OF THE ACADEMY OF [1898. the middle of the right margin of the lung cavity in some genera (Ariolimax, Aphallarion, Hesperarion), at the right anterior angle in others (Arion, Prophysaon). The rectum lies along the right side, posteriorly, and opens at the breathing pore (Pl. XV, figs. 73, ete., r). Lying in the lung cavity, and often almost filling it, is the kid- ney (PI. XV, figs. 76, 77, 80, ete., &). It is rounded or squarish in shape, thick, and attached by its upper side’ to the roof of the lung cavity around the heart and toward its posterior side. The kidney appears variously striated or shows branching ducts (as in Pl. XV, fig. 74). Its secretion is voided through a slender duct the (second- ary ureter, Pl. XV, wu. 7) emerging posteriorly toward the right side, running parallel to the rectum, and opening near the edge of the breathing pore. The characters of the ureter are insufficiently shown in the figures. Behind the middle of the kidney there is an excavation perforating it, occupied by the heart (PI. XV, a.v.). In some genera both chambers of the heart are exposed below; in others only the ventricle. Only in Aphallarion are both auricle and ventricle concealed by a thin outer layer of the kidney. We have occasionally observed a portion of the kidney protruded tongue-like from the breathing pore in drowned specimens of large species. The morphology of these organs is not greatly varied among the genera of Arionide, and need not be farther considered here. In defining the families of Pulmonata, these organs give characters of great value. II. CLASSIFICATION. The generic characters of slugs in general, and of Arionide in particular, as given in the standard manuals and faunal monographs, are of the most superficial character. With a single conspicuous, exception," we do not know of any writer who has given evidence of much insight into or comprehension of the meaning of the varied internal structure of slugs, or who has even suggested a phylogenetic arrangement ot the genera of Arionide. The complete classification of this and related families cannot be presented here without unduly extending the limits of this paper by including information upon the Old World genera; but so far as the Arionide are concerned, the essential outlines may be gathered © Or, as the preparation lies, its lower side. 1! Need we mention the brilliant author of Die Nachtschnecken der Portu- gesisch-Azorischen Fauna? 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 227 from the table below, as all of the subfamilies are represented by American genera. Analytical key to subfamilies and genera. I. Retractor muscles of pharynx and tentacles converging back- ward, their posterior insertions contiguous, inserted at the pos- terior edge of the diaphragm. a. Tail solid, the viscera crowded forward and elevated into a dorsal hump or visceral dome; shell partly or wholly ex- posed ; penis present, with retractor muscle; ovo-testis posterior in the body-cavity; intestine short and simply folded ; an accessory “retensor ” muscle developed. Subfamily BINNEYINE. b. Shell exposed, spiral, Vitrina-shaped, with differen- tiated, lirate or costulate nepionic whorl; mantle with small lobes on each side of the breathing orifice ; sole distinctly tripartite; genitalia with accessory organs, the penis retractor inserted on the diaphragm ; retensor muscle short, slender, toward the right side ; buccal retractor shortly bifurcate anteriorly. BINNEYA. b’. Shell partially exposed, a flat or convex, non-spiral plate; no lobes on the large mantle; sole not in the least tripartite; genitalia without accessory organs, the penis retractor muscle inserted on the “ retensor,” which is strong, wide, and to the left of the buccal retractor, the latter not bifurcate anteriorly, HeMPHiLuiia. a’, True slugs, the foot excavated throughout, the body-cavity (and viscera) extending to the tail; shell small, flat, not spiral, wholly buried ; ovo-testis anterior to the posterior loop of intestine; intestine long, spirally twisted; inner cusps of outer lateral and inner marginal teeth much lengthened ; pharynx retractor deeply bifurcate anteriorly. Subfamily ARLOLIMACINE. ” b. A well-developed “ retensor” muscle present ; geni- talia with no appendicula, the ovo-testis anterior in position; tail with a “plug” in the caudal pore. Large slugs. 228 PROCEEDINGS OF THE ACADEMY OF [1898. c. No penis nor penis retractor muscle, the vagina assuming its function; a small epiphallus ; right eye retractor not passing between male and fe- male branches of genitalia, APHALLARION. ec’. Penis large, introverted apically, with well-de- veloped retractor muscle; right eye retractor involved between male and female branches of genitalia, ARIOLIMAX, b’. No retensor muscle; an appendicula on the atrium; penis simple, with apical papilla and a well-devel- oped retractor muscle; caudal pore an open pit; foot-margin wide. Slugs of moderate size, HEsSPERARION, II. Retractor muscles of pharynx and tentacles running parallel, the latter inserted proximally at the outer posterior angles of the diaphragm; (in American genera the penis and its retractor muscle wanting, the free oviduct or the vagina assuming its function) ; epiphallus variously modified. True slugs, with com- pletely buried shell plate or vestige, and visceral cavity extend- ing into the tail. Subfamily ARIONIN EE. a. Retractor muscle of the pharynx inserted proximally de- cidedly behind the posterior edge of the diaphragm ; intes- tine long and strongly twisted spirally, the stomach, or posterior loop formed by G' and G’, lying behind the loop formed by G* and G‘; kidney ring-like, exposing both chambers of the heart from below. b. Epiphallus slender, tapering distally, not abruptly bent or constricted near the atrium; spermatheca duct inserted upon the atrium; free oviduct fune- tional as a penis; ovyo-testis extending behind the intestine ; external integument longitudinally rugose ; sole more or less visibly tripartite; a mucous gland at the tail; breathing pore decidedly anterior to mid- dle of mantle, the genital orifice below it, ARION. — a’. Retractor of the pharynx inserted at the posterior edge of the diaphragm ; intestine shorter, not much twisted spir- ally, the stomach, or posterior loop formed by G' and G’, lying far anterior to the posterior loop formed by G* and G*; external genital orifice anterior, near right tentacle. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 229 b. Sole not in the least tripartite; posterior portion of the tail peculiarly modified and capable of self-ampu- tation; kidney with a large excavation exposing both chambers of the heart ; epiphallus more or less swol- len, suddenly constricted and bent near its insertion in the atrium, with which it communicates by ashort pedicel which is bound to the swollen portion of epi- phallus by a muscular band; vagina functional as a penis ; ovo-testis lying in front of the posterior loop of the gut, PROPHYSAON. b’. Sole tripartite, the narrow median field defined by longitudinal grooves; tail normal; kidney covering the auricle (seen from below); genitalia unknown, ANADENULUS. III. DESCRIPTIONS OF GENERA AND SPECIES. Genus BINNEYA J. G. Cooper, 1863, Binneya Cooper, Proc. Cal. Acad. Sci., III, p. 62. Xanthonyx Crosse & Fischer, Journ. de Conchyl.. XV, 1867, p. 223; Moll. Terr. et Fluv. Mex., I, p. 192. Strebel & Pfeffer, Beitrag zur Kenntniss der Gant Mexikanischer Land- und Siisswasser Conchylien, Theil IV, p. 26 1880). Somewhat slug-like, with elevated, subspiral visceral hump and external shell, subcentral on the back; mantle broadly produced beyond the shell, not reflexed over it at edges; breathing pore sub- median or behind middle of right margin of mantle, a small rounded left and somewhat larger right cervical mantle lobe on each side of it; genital orifice behind the right tentacle; foot radially grooved and reticulate above, the foot-margin narrow; pedal grooves deep, without a tail pore; sole tripartite, the areas separated by longitudi- nal grooves; shell Vitrina-shaped, with the first (nepionic) whorl distinctly demarked from the following, and strongly sculptured. Viscera elevated into the dorsal hump, the body cavity not ex- tending back of it into the tail, which is solid. Jaw arcuate, with numerous ribs denticulating the basal margin. Radula with 28-1-28 to 31-1-31 teeth (in B. notabilis), 32- 1-32 (in B. cordovanus), the rachidian teeth tricuspid, laterals bi- cuspid, the ectocones small; marginal teeth bicuspid, the inner cusps moderately long, sometimes bifid. Intestinal tract (PI. XI, fig. 81) short; anterior loop formed by G’ and G* somewhat twisted, posterior loop of G* and G* straight 230 PROCEEDINGS OF THE ACADEMY OF [1898. and very short. Liver occupying posterior portion of dorsal hump and spire of shell. Genital system with well-developed penis continued beyond inser- tion of retractor in a short epiphallus. Spermatheca with a long duct or one of quite moderate length; an appendicula near the base of vagina or penis, and, according to Pfeffer, two long-stalked, globose, netted vaginal accessory appendages. Muscle system (PI. XIV, fig. 65) Ariolimacine. Buccal and eye’ retractors converging posteriorly, contiguous at their proximal in- sertions. A “retensor” arises from the roof of visceral cavity slightly anterior to proximal insertion of retractors, and extends anteriorly to the right side near the lower edge of mantle, where it is inserted in the integument. Penis retractor inserted in the left posterior region of the visceral dome. Distribution, Santa Barbara Island, off California, Guadalupe Is- land, off Lower California (B. notabilis), and States of Vera Cruz and Chiapas, Mexico (B. Salleana, Cordovana, Sumichrasti, Chia- pensis). The chief differences between Binneya and Xanthonyx seem to be that in Binneya the nepionic shell is spirally lirate, in Xanthonya radially plicate; in Xanthonyx there is a small caudal horn, in Binneya none; and there are certain discrepancies in the details of genitalia as described by Binney, Crosse and Fischer, and Strebel and Pfeffer. These may, perhaps, be in part merely specific varia- tions, and in part errors of observation. On account of the sexually immature condition of our specimens we unfortunately cannot verify the published accounts. The description of the anatomy of Xan- thonyx Salleanus given by Strebel and Pfeffer seems to be worthy of confidence. Binneya agrees with Hemphillia in the solid tail, the viscera being crowded forward into the dorsal hump; in the exposed shell, short and simple gut; the general arrangement of muscles, especially the possession of a “ retensor”’ ; in the well developed penis, and general system of external reticulation. It differs from Hemphillia mainly in the better developed spiral shell, the differently placed retensor — muscle and penis retractor, the presence of an appendicula, and the — distinctly tripartite sole. That the two genera are closely allied is — so obvious as to justify the supposition that Hemphillia descended from a slug very similar to the existing Binneya. Cryptostrakon W. G. B. is probably allied to Binneya, but the 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 231 muscles, genitalia and alimentary canal are unknown, and the types though in alcohol, have been dried. B. notabilis J. G. Cooper. Pl. XIV, figs. 63, 64, 65; Pl. XVI, figs. 87, 88. Binneya notabilis J. G. Coop., Proce. Cal. Acad. Sci., III, p. 62, figs. 15, in text. Tryon, Amer. Journ. Conch., II, p. 244, pl. 3, f. 4 (copied from Cooper). W. G. Binney, Land and Fresh-water Shells of N. A., I, p. 68, f. 112. Terr. Moll., V, p. 245, f. 141-143; pl. V, f. K (teeth), pl. xi, f. B (genitalia). Man. Amer. Land Shells, p. 108, f. 71-74. Fourth Supplement to Terr. Moll. V, p. 184, pl. 1, f. 9 (shell). Alcoholic specimens measure about 10 mm. long to double that length; color buff-gray with rather large black dots mainly scattered along the radial grooves of the foot and in a line above the pedal grooves, the mantle maculated with black. Surface with rather coarse radial grooves and sparse reticulation ; a fine groove median on tail above, not extending to the end ; foot margin narrow, closely and evenly crenate ; sole unicolored grayish, rugose and distinetly tripartite. Jaw (Pl. XVI, fig. 87) and dentition (Pl. X VI, fig. 88) described above. Digestive and muscular anatomy described above.» Our spec- imens were sexually immature, so that the description of genitalia is taken from Binney, Crosse, Fischer, Strebel and Pfeffer. Distribution : Santa Barbara Island, off California; Guadalupe Island, off Lower California. Genus HEMPHILLIA Bland & Binney, 1872. Hemphillia Bland & Binney, Ann, Lye. N. H. of N. Y., X, p. 208 (1872), type H. glandulosa B. & B. Slug-like, with the mantle conspicuously elevated (in alcoholic specimens) into a nonspiral visceral hump; the shell a slightly convex, non-spiral plate partially exposed, its edges buried in the mantle, which is very broadly produced beyond the shell on all sides. Breathing pore behind the middle of right margin of mantle. Genital orifice behind the right tentacle. Foot radially grooved and reticulate above, the foot margin wide, conspicuous ; pedal furrows deep, meeting in a mucous pore at the tail, or without tail gland. Sole not in the least tripartite. Viscera elevated into the dorsal hump, the body-cavity not extend- ing back of it into the tail, which is solid. Jaw low, wide, with about 14 low wide ribs with shallow intervals, Radula with tricuspid central, bicuspid lateral and marginal teeth, the inner cusp (mesocone) of the latter long. 232 PROCEEDINGS OF THE ACADEMY OF [1898. Intestinal tract short, crowded forward, but little twisted ; G* angularly bent, forming a sort of fifth fold (Pl. XI, fig. 36). Genital system with well developed penis containing penis-papilla, the retractor terminal; passing intoanepiphallus. Spermatheca on a short duct, inserted in atrium; ovotestis at posterior end of vis- ceral cavity, immediately under hind end of shell. Muscle system Ariolimacine, the eye and buccal retractors con- verging posteriorly, contiguous at their proximal insertions; buceal retractor spreading where it enters buccal mass, not bifurcate. A broad “ retensor” muscle arises at the posterior margin of diaphragm just left of the retractor insertions, and runs forward as far as the front insertion of the mantle (Pl. XIV, fig. 69, ret.). Penis retrac- tor inserted proximally on the ventral face of the retensor. Right eye retractor passing between male and female branches of the genitalia. Lung radially striate rather than reticulate. Kidney a broad squarish leaf, free for the greater part, adnate dorsally around the heart, (Pl. XV, fig. 78). Distribution ; Oregon, Washington and western Idaho. Hemphillia shares with all Ariolimacine the primitive arrange- ment of the retractor system. Like all of this subfamily except Hesperarion it possesses that anomalous muscle called by Simroth the “retensor,” which we hold to be a modified retractor pedis. Apart from these important characteristics of the musculature, there are profound differences from Ariolimaz and its allies: the viscera are crowded forward and upward into a visceral hump under the mantle, behind which the foot is solid, as in the spiral-shelled snails; the shell is comparatively large and imbedded only at the edges in the mantle, which exposes a considerable part of it; and the intestinal tract, while fundamentally of the same type, is con- siderably shortened and simplified. In all of these departures from the normal slug structure, Hemp- hillia is akin to Binneya; but it is a more advanced evolution-pro- duct, in that it has lost the spiral torsion of the visceral mass and shell, still retained by Binneya as a reminiscence of long past ances- tors. Among the secondary characters separating Hemphillia from Binneya may be mentioned the tripartite sole, narrow foot margin, and small mantle lobes of Binneya, the other genus having no divis- ion of the sole, no mantle lobes and a wide foot margin. Internally, 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 233 Binneya has an appendicula, the penis retractor is inserted on the lung floor, and the retensor muscle is weak, while in Hemphillia there is no appendicula and the penis retractor is inserted on the surface of the very broad and strong retensor. The digestive tract is considerably alike in the two genera. Key to species of Hemphillia. a. Mantle papillose; tail acutely keeled above, terminating in a fleshy horn which overhangs the caudal pore; pedal furrows scarcely rising at their union behind. Penis with a bifid inter- nal process inserted at the apex of the cavity ; spermatheca glob- ular, on a comparatively slender duct; penis retractor muscle inserted upon the epiphallus, . . . . . . . . H. glandulosa. a’. Mantle slightly rugose, not papillose; no horn at tail; pedal grooves abruptly rising behind, meeting over the tail. Penis with a simple fleshy process inserted at the base of the cavity ; spermatheca small with a very stout duct ; penis retractor muscle SEENON i ws Nanay gf bp nn: « + J, Comtelue, H. glandulosa Biand & Binney. PI. IX, figs. 1,2; Pl. XII, figs. 49, 50. Hemphillia glandu/osa Bland & Binney, Ann, Lyc. Nat. Hist. of N. Y., X, p- 209, pl. ix, f. 1, 3 (exterior), 5 (shell), 15-17 (teeth), Terr. Moll., V, p. 248, f. 144-146, pl. v, f. J (teeth), pl. xii, f. J, K (genitalia) ?. Man Amer. Land Shells, p. 111, f. 75-77 (78?)._ Supplement to T. M., V, pl. iii, f. Hi (?). Third Supplement, p. 211, pl. iv, f. D. Pilsbry & Vanatta, Nautilus XI, p, 44. Color in alcohol blackish above, or yellowish with black spots; the edge of mantle, sides of foot below mantle, foot-margin and sole yellowish; shell yellow. Mantle extension densely papillose in front of the shell and at sides. Breathing pore median on the right side. Genital orifice near right tentacle, a groove running from it toward the breathing pore. Foot obliquely grooved and rather coarsely reticulated, pinched up into a high, acute keel posteriorly, this keel declining and terminating in a prominent horn-like process atthe end, Foot-margin rather wide, vertically grooved as usual. Pedal furrows scarcely rising at the tail, meeting in a caudal pore immediately below the “horn.” Sole transversely wrinkled, the wrinkles bent backward mesially, as in Prophysaon. Length 10 to 13 mm. Shell convex, with yellow cuticle, thin calcareous layer and pos- terior nucleus. Genitalia (P|. XII, figs. 49, 50) with the penis enormously swollen, its lumen filled by a bifid, fleshy, imperforate, corrugated body 16 . 234 PROCEEDINGS OF THE ACADEMY OF [1898. attached to one side above; epiphallus moderately stout, longer than the penis, bearing the retractor muscle near its base. Sperm- atheca globular, large, borne on a duct of its own length, inserted upon the atrium. Type locality, Astoria, Oregon (Hemphill); also in Washington — at Chehalis; and according to Binney, Olympia and Gray’s Har- bor. Part of several of the references given above apply to H. came- lus, Mr. Binney having included that species in glandulosa. The latter is herein restricted to slugs with papillose mantle and caudal horn, as originally indicated by Bland and Binney. Besides the conpsicuous external differences noticed under H. camelus, the two species differ markedly in the genitalia. In H., glandulosa the fleshy process in the penis is bifid and attached to the side at the apex of the cavity. In H. camelus the process is simple and attached basally. The position of the penis-retractor and the shape of the spermatheca and its duct differ in the two forms. H. camelus Pilsbry & Vanatta, Pl. IX, figs. 3,4; Pl. XII, figs. 41, 42; Pl. XVI, fig. 85. Hemphillia camelus Pilsbry & Vanatta, Nautilus, XT, p. 44 (August, 1897). Color in alcohol pale grayish-buff, closely speckled and maculated with blackish on the mantle and tail, more sparsely and lightly so on the anterior half of the foot, the sole without dark markings. On the mantle the spots form two more or less distinct longitudinal bands. Surface of the mantle somewhat rugose, not papillate ; breathing pore behind the middle. Genital opening near right tentacle. Foot with a short dorsal groove behind mantle, obliquely descending grooves with sparse reticulation on the sides of tail, and coarse reticulation below mantle laterally ; the head longitudinally closely grooved and reticulate ; sole as in H. glandulosa; tail some- what keeled above near the end, without any appearance of a cau- dal “horn.” Foot-margin wide, grooved vertically ; pedal furrows abruptly and conspicuously rising at the tail, with no noticeable caudal pore at their union, at least in alcoholic examples, but in one specimen there seems to be a transverse slit under the pedal groove, with a vertical gutter below it, T-shaped. In another, nothing of this appears. Length about 28 mm. Genitalia (Pl. XII, fig. 41, 42) with a very large penis, its cavity filled by a large, transversely corrugated, solid, fleshy body attached at the base of the penis, and a small tongue-like body arising close 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 235 to the entrance of the epiphallus (fig. 42). The latter is longer than in H. glandulosa, and the retractor muscle is inserted at its root. Spermatheca small, its duct very stout, inserted upon the atrium. Shell slightly convex, long-oval, with clear yellow cuticle, thin calcareous layer, and posterior nucleus; thesurface lightly marked with growth lines. Length 8, width 5 mm. Jaw low, wide, with about 14 low, broad ribs separated by nar- row intervals. Radula: Marginals with rather long inner cusps (Pl. XVI, fig. 85). Old Mission, Idaho (Henry Hemphill). This species has a proportionally smaller shell than H. glandulosa, a longer, less compressed and less carinated tail, with no trace of a caudal horn and no perceptible caudal gland; the mantle is not papillose, the pedal furrows rise abruptly at the tail, uniting over it, and the genitalia differ in important respects, as noticed under the description of H. glandulosa. Genus ARIOLIMAX Morch, 1860, Ariolimax Mérch, Malak. Blatter, VI, p. 110. Pilsbry & Vanatta, Proc. Acad. N. 8. Phila., 1896, p. 342. To the generic characters described and implied in our former paper, the following may be added : Tail gland (P]. XV, fig. 81) a peculiar triangular mass of tissue, in aleoholic specimens deeply fissured transversely. Muscle system (PI. XIV, fig. 66, A. columbianus) having the buccal and eye retractors converging posteriorly, their proximal in- sertions contiguous at the posterior edge of the diaphragm. Bue- cal retractor very deeply bifurcate. An accessory muscle, the “ retensor,” arises with the retractor group, to the left of the median _line, and passing forward is inserted. i in the integument of the neck, on the right side or above. Lung (PI. XV, fig. 73, A. columbianus, the kidney removed) and kidney (Pl. XV, fig. 74, A. columbianus) as usual in Arionida, Auricle concealed by kidney, ventricle (fig. 78, 74, v) exposed. Subsequent studies support the conclusion reached in our former paper, that Ariolimaz is more closely allied to Aphadlarion than to any other known genus. Genus APHALLARION Pilsbry & Vanatta, 1896. Aphallarion P. & V., Proc. Acad. N. 8. Phila., 1896, p. 348. Tail pore as in Ariolimaz. Muscle system (PI. XIV, fig. 67) substantially like Ariolimaz in arrangement of the buccal and eye retractors, except that the right 236 PROCEEDINGS OF THE ACADEMY OF [1898. eye retractor is not involved between the ¢ and @ branches of genitalia; ‘“‘retensor” inserted nearer the median line anteriorly. Penis retractor wanting, but several vaginal retractors (fig. 67, vag. 7.) arise from the diaphragm. Pallial region as in Ariolimax, except that the kidney is larger, and both auricle and ventricle are concealed therein (Pl. XV, fig. 76). Aphallarion is intimately related to Ariolimax, from which it dif- fers in the absence of a penis and its retractor, in having the right eye retractor free from and to the left of the genitalia, and in havy- ing both chambers of the heart embedded in the kidney. No other genus is nearly allied. To our former account it may be added that Mr. Wetherby in- forms us that his Ariolimax Hecowxi from Santa Cruz is specifically the same as our A. Buttoni. As he remembers the genital system, it corresponded with that of our species. Since A. Hecowi was not described, this will in no way affect nomenclature, but is of interest as removing a doubtful species from slug literature, and extending the geographic range of Aphallarion. Genus HESPERARION Simroth, 1891. Hesperarton Simroth, Malak. Blitter (n. F.) XI, Heft 2, p. 109. Type Ariolimax niger Coop. Slugs with the usual small, anterior, shield-like mantle, completely buried, non-spiral shell plate, and long body-cavity excavated to end of tail. Breathing pore somewhat behind middle of right mantle edge. Genital orifice distant from tentacle, below the ante- rior margin of mantle. Foot with longitudinal grooves, becoming oblique on the sides, the foot margin moderate, pedal furrows deep, meeting in a very conspicuous, subtriangular, posteriorly guttered tail pit. Sole rather indistinctly tripartite, the areas not defined by longitudinal grooves. Jaw with coarse ribs. Radula with the usual tricuspid central and bicuspid lateral teeth, ectocones small; marginals with very long, oblique cusps, the ectocone minute or vestigial. Intestinal tract (Pl. XI, fig. 33) muchas in Ariolimaxz. G" in- distinctly divided into crop and stomach, making a half revolution ; G describing a complete revolution in the opposite direction, G° another, reversed, and G* still another revolution parallel to G’. Posterior loop formed by G* and G‘ lying behind that formed by G' and G’, as in Ariolimacine generally. —— |" — | 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 257 Genital system (Pl. XII, figs. 44-48) having a well developed penis with terminal retractor and epiphallus, lumen with plicate walls (fig. 45), and a large apical penis papilla (figs. 45, 46). Atrium bearing a vermiform appendicula with swollen base (fig. 44 ap ; fig. 47,ap). Spermatheca borne on ashort, basally swollen duct. Spermatophores (fig. 43, x 13) cbitinous, elongate, with flagellum- like extension at oneend. Ovotestis separated from albumen gland, lying on the right side under G’*, to the right of posterior end of stomach (Pl. XI, fig. 33, ot.). Muscle system (PI. XIV, fig. 71) Ariolimacine in having the re- tractors converging posteriorly, their proximal insertions contigu- ous; buccal retractor deeply bifurcate. No “retensor.” Penis retractor short, broad, inserted in the left anterior portion of the lung floor or diaphragm (fig. 71, r. p.). Lung as usual; kidney very large (Pl. XV, fig. 77, &). Only the ventricle exposed. Distribution : Middle portion of California, in the counties lying near and below San Francisco Bay, west of the Sierra Nevada. Externally Hesperarion is like Ariolimax and Aphallarion except in the structure of the caudal pore, which is a deep, open pit in this genus, while in the others it is filled by a mass of spongy tissue. The jaw, teeth, intestine, pallial region and musculature of the three genera are practically identical in their main features, except that Hesperarion totally lacks a “ retensor” muscle. In the genitalia are found further important differences. The ovotestis is not packed adjacent to the albumen gland anteriorly, as in Ariolimaz and Aphallarion, but is carried back to a more pos- terior position among the hind loops of the intestine, and surrounded by the liver (PI. XI, fig. 33, of.). The penis, externally similiar to that of Ariolimaz, is of the usual simple structure, not invagi- nated, and the atrium bears an enigmatic organ of unknown fune- tion, our ignorance of which is veiled behind the term “ appendic- ula.” This is wanting in other Arionide with the exception of Binneya, the most primitive genus of the family. The species of Hesperarion are dimorphic, like Ario/imax colum- _ bianus, having a spotted and an immaculate form, This convenient term was first used by Dr. von Ihering in his “ Morpholo- gie und Systematik des Genitalapparates von Helix.’’ The appendicula in- serted low on the vagina or on the atrium is not homologous with the elon- ted sack found in Panda, Strophocheilus, ete., associated with the spermatheca. he latter probably serves the purpose of an accessory spermatheca, 238 PROCEEDINGS OF THE ACADEMY OF [1898. H. niger (J. G. Cooper). Pl. IX, figs. 5,6; Pl. XI, fig. 33; Pl. XII, figs. 43-48; Pl. XIV, fig. 71. Ariolimax niger J. G. Cooper, Proc. Acad. Nat. Sci. Phila., 1872, p. 147, pl. 3, f. B, 1-4. W.G. Binney, Terr. Moll. V, p. 234, f. 183 (caudal pore) ; pl. v, f. D, F, (teeth) ; pl. xii, f. F (genitalia); Man. Amer. Land Shells, p. 100, f. 64; Terr. Moll. v, Third Supplement, Bull. M. C. Z., XIX, no. 4, p. 212, pl. v, f. A, I, C, D (external aspect and caudal pore). Cockerell, Ann. Mag. N. H. (6), vi, p. 278, 279. Wigal niger Simroth, Malak. Blitter (n. F.), xi, p. 109-119, pl. 1, f. 7-14. Ariolimax Andersoni J. G. Coop.?, W. G. Binney, Ann. Lyc. Nat. Hist. N. Y., xi, p. 182, pl. xii, f. 9 (genitalia), pl. xviii, f. G (teeth); Terrestr. Moll. V, p. 235, f. 135, 136, pl. xii, f. E (genitalia), pl. v, f. G (teeth). Man. Amer. Land Shells, p. 132, f. 66, 67. Second Suppl. T. M. V, p. 43. Third Suppl. p- 212, pl. v, f. F. Not Arion Andersoni J. G. Cooper. Exterior: Upper surface (in alcoholic specimens) smoky brown- black above, slightly lighter gray-black laterally, unicolored or dappled with black ragged spots; sole gray-black, with black spots scattered along the inner edge of the lateral areas. Integument obliquely longitudinally grooved, not much reticulated. Mantle with the lung pore submedian ; genital orifice some distance behind the right tentacle, caudal pore conspicuously large and deep, witha cleft extending to the tail ; sole indistinctly tripartite. Length (in aleohol) 30-45 mm. The genitalia in two individuals dissected show considerable variation. In one, (Pl. XII, fig. 44), the penis is large nearly its entire length, constricted at base; this being from a maculated indi- vidual like Pl. IX, figs. 5, 6, from Santa Clara, Cal. In the other, a typical niger in coloring, the penis is slender below, swollen above (Pl. XII, fig. 47). We hope to receive further specimens and ascertain the limits and significance of variation in these organs. In one specimen (Mus. no. 71,078) there were thirteen spermato- phores (P]. XII, fig. 45) in the spermatheca. Jaw with eleven wide ribs. tadula agreeing with Ariolimaz in the long, oblique cusps of the marginal teeth. Cooper’s types were from the neighborhood of San Francisco Bay. Specimens are before us from Bolinas, Haywards, Santa Clara, Stevens’ Creek Canyon, Santa Cruz range, 900 feet altitude, and near San José. Binney gives the localities Santa Rosa, Healds- burg, Sonoma Co.; and for the synonymous Ariolimaxz Anderson, mountains of Alameda Co. The general range, therefore, covers the Coast and Bay counties from Sonoma to Santa Cruz. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 239 Professor Cockerell defines a color-form maculatus as follows: “This much resembles A. hemphilli var. maculatus, but is larger and stouter, and has the lateral areas of the sole marbled as in niger. Two specimens were received from Dr. Cooper, who found them at Haywards, Cal.” The maculated form is shown in our figures. It seems more abundant than the spotless slug, but in our series it is difficult to separate the two, as some which appear spot- less often show a few macul on close examination. H. Hemphilli (W. G. Binney). Ariolimax HemphilliW.G. Binney, Ann. Lyc. Nat. Hist. N. Y., XI, p. 181, pl. xii, f. 7 (genitalia), pl. xviii, f. H (teeth) (1875); Terrestr. Moll., V, p. 235, f. 134, pl. v, f. H (teeth), pl. xii, f. G (genitalia) ; Man. Amer. Land Shells, p. 102, f. 65. Third Suppl. Terr. Moll., v, p. 212, pl. v, f. G. Cock- erell, Ann. Mag. N. H. (6), vi, p. 278. Ariolimax Hemphilli yar, maculatus Ckll. in Binney, Third Supplement to Terr. Moll., V, p. 212, pl. v, f. B. Since its first publication in 1875, nothing material has been added to our knowledge of this species. Its generic position is un- certain. The desirability of procuring additional specimens in order to place the form upon a better basis will be evident. The type locality is Niles Station, Alameda Co., California. Professor Cockerell’s color-form maculatus has been figured in Binney’s Third Supplement, but not before described. “Small spotted hemphilli found by Dr. Cooper at Haywards. When alive, as I learn from Dr. Cooper, they are reddish, the spotted variety of niger being gray; in alcohol, both appear gray. They agree with hemphilli W.G. B. in the genitalia, and differ also from niger in their more slender form and immaculate sole of foot. Indeed, com- paring them with typical niger, they appear fundamentally distinct in every way, but the var. maculatus of niger is strangely interme- diate—just what one might expect a niger * hemphilli hybrid to be.” (CkIl. ma.). Genus ARION Ferussac. Conspicuous in the European fauna for the number of species and individuals, and forthe large size and frequently brilliant col- oring of some forms, this genus is represented in America by one or two species introduced from Europe and still very local in distribu- tion. They have not yet exhibited the tendency to spread charac- teristic of the introduced Limaces. Arion hortensis Fér. Pl. XV, figs. 79, 82, 83; Pl. XIV, fig. 72. Numerous specimens of this species were collected in March and April, 1896 near or in a greenhouse in Seattle, Washington, by Mr. 240 PROCEEDINGS OF THE ACADEMY OF [1898. P. B. Randolph. A specimen much contracted in alcohol is here figured, with the retractor system and pallial organs. As preserved they measure 15 to 20 mm. in length; ground-color above dirty whitish, with a.conspicuous blackish stripe along each side of mantle and of the foot behind it, the back with a broad median bluish or slate-black band, tapering posteriorly, often only faintly indicated ; sole light yellow. In other specimens from Poughkeepsie, N. Y., the region between the longitudinal black bands on mantle and sides is speckled and maculated with black. As this species is an immigrant from Europe, where it is well known and has been repeatedly investigated anatomically, we omit a detailed description and synonymy. The coarsely, longitudinally rugose integument, anterior position of the breathing orifice, and posterior position of the genital orifice, below the other, readily dis- tinguish Arion from all native American slugs. Arion sp. W. G. Binney describes a slug referred by him to Arion fuscus Miller, from Boston, Mass. Mr. Cockerell considers it likely that the figure in Terrestrial Mollusks, Pl. LXIV, fig. 1, (copied in Man. Amer. L. Shells, fig. 502) represents A. subfuscus. Whether more than one species of Arion occurs in America will remain doubtful until further examination of the Bostonian slug can be made. Genus PROPHYSAON Biand & Binney, 1873. Prophysaon Bland & Binney, Ann. Lyc. Nat. Hist. N. Y., X, 1873, p. 293; type P. hemphilli B. & B. Cockerell, Ann. Mag. N. H. (6), VI, p. 277-279, and Nautilus XI, p. 77 (key to species).—W. J. Raymond, Nautilus, IV, p.6 (mutilation of tail). Phenacarion Cockerell, Nautilus III, p. 127 (March, 1890), type Arion foliolatus Gld. The Conchologist II, p. 118. Siugs with anterior shield-like mantle in which the flat, non-spiral shell is completely buried, the breathing pore in front of the middle of its right margin ; genital orifice behind and near right tentacle. Foot reticulated, the areole subdivided (except in cwruleum) ; the coloration in two or three longitudinal bands on mantle or mantle and foot, or monochromatic. Foot-margin wide, pedal furrows deep, with no noticeable caudal pore (or only a small slit, in P. foliolatum, hardly or not visible in alcoholic specimens). Sole not in the least tripartite. Tail usually showing an oblique constriction at from the posterior third to sixth of the animal’s length, marking the place where self-amputation takes place. eS a ee ee ————E—————«oxo - es a oe 1898.] NATURAL SCIENCES OF PHILADELPHIA. 241 Body cavity extending into the foot, but frequently not to its end ; genital system and gut lying side by side and extending about the same distance backward (Pl. XI, fig. 34, P. fasciatum). Jaw weak, flexible; flatly ribbed, plaited or striate. Rachidian teeth tricuspid, laterals bicuspid, the ectocones small; marginals formed by shortening of the basal-plates, bicuspid, the mesocone moderate or short, ectocone small, occasionally bifid. Intestinal tract (PI. XI, figs. 28, P. Andersoni ; fig. 30, P. ceruleum, fig. 32, P. foliolatum, and fig. 34, P. faseiatum) with four well devel- oped sigmoid folds; no division of G' into crop and stomach ; ante- rior loop formed by G’* and G* twisted one-half revolution ; poste- -rior loop of G* and G* long, extending far behind stomach, and twisted less than a complete revolution. Genital system (Pl. XII, figs. 37-40, and Pl. XIII, all figs.) not crowded forward; no penis nor retractor; epiphallus either very stout, cylindrical and fleshy, with minute perforation, or more slender, long and tapering distally ; in either case suddenly narrow- ing near the atrium to a minute duct, which enters the atrium by a short tapering peduncle, in close contact with which the enlarged epiphallus is held by a muscle (seen in fig. 57 of Pl. XIII, muse., and fig. 39 of Pl. XII). Duct of spermatheca short ; spermatophores as in Hesperarion. Ovotestis (Pl. XI, fig. 34) lying anterior to the posterior loop of gut, between its upper and lower folds, adjacent to the albumen gland. Muscle system (PI. XIV, fig. 70) with the eye retractors inserted at the outer posterior angles of the diaphragm, as in Arion; buecal retractor inserted at the posterior edge of diaphragm to the right of the middle, bifurcate distally. Right eye retractor passing between branches of genitalia. Pallial region (PI. XV, fig. 80) much as in Arion; breathing pore, anus and nephridial orifice at the right anterior angle of the pallial cavity ; kidney ring-like, excavated to show both chambers of the heart; other features as usual in the family. Distribution: Middle California to British Columbia, eastward in Idaho to the Cour d’Aléne Mts. Prophysaon stands rather isolated in the Arionine. The only native American genus approaching it is Anadenulus, but this differs in several important particulars to be mentioned below. The Pale- arctic Arion is like Prophysaon in the pallial region, but differs markedly in (1) the removal of the buccal retractor insertion back- 242 PROCEEDINGS OF THE ACADEMY OF [1898. ward from the diaphragm edge, (2) the complex twisting of the gut and the posterior position of the stomach (see these Proceedings, 1896, pl. 18, f. 3) ; (8) the simpler form of the epiphallus, and well developed retractor muscles of vagina and spermatheca, and (4) the normally constructed tail. There are various other minor differences; but upon the whole, the American genus is less divergent than the European from the primitive forms of the family in its musculature, more diver- gent in the tail structure and epiphallus. In Arion, shell reduction has progressed rather further, at least in thetypical forms. Geoma- lacus, a lateral branch from the Arion stem, is even more remote from the American genus. The Himalayan genus Anadenus (with which Fischer unites Prophysaon as a subgenus), differs conspicuously in possessing a well developed penis with retractor, and externally in the extreme narrowness of the foot margin and the tripartite sole. The self-amputation of the tail in Prophysaon has been described by Henry Hemphill® and W. J. Raymond ;* while Simroth has noticed and figured the appearance of the tail in alcoholic specimens before amputation. Mr. Raymond writes as follows: “In August, 1888, I collected on one occasion about a dozen examples of Prophysaon Andersoni J. G. Cp., near the San José reservoir, above Lexington, Santa Clara County. While taking measurements of the living specimens, before putting them into alcohol, I noticed in several a contraction about two-thirds of the length from the head. This appeared as an indented line completely encircling the body. Upon handling the slugs to examine this phenomenon more closely, the line became deeper and in the case of two of the specimens the tail dropped off, almost as readily as the ray of the so-called ‘ brittle’ starfish.” Nearly all full grown alcoholic specimens of P. Andersoni, folio- latum and ceruleum show a well defined impressed line around the tail, or occasionally the tail has actually been amputated, as in the specimen of the last-named species figured on Plate IX, figs. 7 to 11. Dissection shows that the body cavity does not extend beyond the point of excision, or but little beyond; the remainder of the tail being occupied by very spongy vesicular connective tissue. We have not seen Prophysaon alive, and observations are still lacking ao some ier points which slots pee uaEny be sup- 3 Nautilus II, p- 126, Eprnnie: Fourth Buuclemana to Terr. Moll. V, p. 182. 14 Nautilus LV, p. 7. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 243 plied by keeping slugs in captivity. Does regeneration of the lost member take place, and if so, is the renewed tail structurally like the amputated one, or does loss of the tail result eventually in death? What animals persecute Prophysaon? Observations upon these questions might go a long way toward explaining the present utility of tail amputation, though they may not indicate the mode of its origin. Without knowledge of the final consquences of am- putation to the slug, or what its natural enemies are, speculation upon tail excision is idle. In an analogous case now well known, that of Helicarion in the Philippine Islands, Semper” states that every species he examined “ possessed the singular property, which many lizards hayve—particularly the Geckos—of shedding their tail when they are seized somewhat roughly at a little way behind the shell. This they do by whisking the tail up and down with extra- ordinary rapidity, almost convulsively, till it drops off; if the creat- ure is held by the tail, it immediately falls to the ground, where it easily hides among the leaves. If it is laid flat on the hand, the rapid wagging movement is strong enough to raise the body with a spring into the air, so that it falls over on to the ground. These snails at first constantly escaped me and my collectors in this way, and not unfrequently we had nothing but the tail left in our hands. According to Guilding’s observations the same peculiarity of part- ing with the hinder prolongation of the foot characterizes the West Indian snail Stenopus. I ascertained by further investigation that in a free state of nature such self-mutilation not unfrequently occurs, for about a hundred specimens of Helicarion gutta, which is ex- tremely common in the north-east of Luzon, I found, perhaps, ten in- dividuals that had shed their tails, or, to speak more accurately, the hinder end of the foot, and had the stumps partly healed, or the foot to some extent grown again. Now, this hinder portion of the foot is the most conspicuous part of the snail’s body, and it may be sup- posed that it is, in most cases, the part first seized by the reptiles or birds that prey upon them ; but, startled by the escape of the body, they would soon learn to recognize, by the form of the tail, those species which were capable, by this self-amputation, of depriving them of the larger and probably the only valuable portion of the prey. In this way the species of the genus Helicarion can escape the pursuit of their enemies better than they otherwise could on account of their exposed mode of life.” % Animal Life, Chapter XII. 244 PROCEEDINGS OF THE ACADEMY OF [1898. Whether Semper’s plausible supposition be held to sufficiently ex- plain the self-mutilation of Helicarion or not, it seems to us that the slowness of the process of amputation in Prophysaon precludes the idea that it is a means of escape from birds, which, in any case, are as likely to seize the slug by the head or middle as by the tail. IEf molluscan foes are in question, the time consumed in amputation is of less moment; and it might be worth while to imprison Prophys- aon with Cireinaria (alias Selenites and Macrocyclis), which is the most rapacious snail of the West Coast. The suggestion is offered for what it may be worth; and the whole subject referred to the enterprising and enthusiastic naturalists of the West for observation and experiment. The species of Prophysaon fall into three very distinct groups, two of them containing but one species each, the other including P. Andersoni Coop. (plus Hemphilli B. & B., Pacifiewn and flavum Ckll.), and P. foliolatum Gld. (including Piccarlan Hemphilli W. G. B.). As the synonymy indicates, these two species are excessively variable. In the case of Andersoni a great extent of territory is in- habited by the several forms and typical form of the species, and much more extensive series than we have yet seen must be brought together before a final decision upon the limits of variation, and the definable subspecies if any exist, can be made. Our study of them is based wholly upon alcoholic slugs, gathered from localities hun- dreds of miles apart; and it is to be expected that richer collections may modify, and certainly will amplify, the conclusions reached. Our general results so far as synonymy is concerned, do not differ radically from those attained by Professor Cockerell, whose synopsis of the species is given below.” 46“ (1), Epiphallus stout, sausage-shaped. A pale dorsal stripe. a. Ochreous species, . . . . . P. Pacificum (incl. favum), b. Grayish species, . . . P&P. Andersoni (incl. Hemphill). “ (2). Epiphallus banana shaped, ‘but tapering attheend. No pale dorsal stripe, . . /P. ceruleum ( Epiphallus rather slender, flattish, tapering, somewhat curved. Shell 2 mm. long, narrow, white, shiny). * (3). Epiphallus slender, gradually tapering to a point. Body with a blackish dorsal band. B/ ORW SiNUed, Peete ss. «5, ake . LP. fasciatum, b. Jaw only striate, . . . LP. Aumile. (Until more material of Aumile is seen, it cannot be made sure that the jaw-character is a specific one. \ For some further details of i peer Cockerell’s views, see Mautilus, Nov. 1897, pp. 77-79. The “banana” or “sausage” shape of the epiphallus we find to be a variable character, not ‘cotidaane specifically. y= SS 1898.] NATURAL SCIENCES OF PHILADELPHIA. 245 Key to species of Prophysaon (aleoholic specimens). a. Surface with coarse diamond-meshed reticulation, the meshes finely subdivided; mantle banded or spotted; foot-margin moderate or wide. b. Mantle free about two-thirds of the distance back to breathing orifice (Pl. X, fig. 17). Epiphallus stout, eylindrical, bluntly rounded at both ends; vas deferens extremely long, convoluted in a snarl; usually a pale dorsal line on the tail ; jaw coarsely ribbed. e. Outer lateral and inner marginal teeth with blunt and rather short cusps. Length 50-80 mm. (in alcohol), the posterior third or more being marked off by an oblique constriction and subject to self- ampieAtion, is) 4 4 6.) ys P. foliolatum. ce’, Outer lateral and inner marginal teeeth with long, acutely pointed cusps. Length 25-35 mm. (in alcohol), the posterior part subject to amputation RMteE Sy nee el ee a a a i Be Aandernons, b’. Mantle free as far back as the breathing orifice (Pl. X, fig.27). Epiphallus slender, gradually tapering distally ; vas deferens not elongated; back with a wide red or pale area enclosing a darker median band, and bounded on each side by dark lateral bands, or entire slug dusky ; jaw closely, finely plaited or striated, P. humile and var. fasciatum. a’, Surface longitudinally closely grooved above, obliquely and less closely so at the sides, the grooves occasionally joined by short transverse lives ; foot-margin very narrow, 1. cwruleum. P. Andersoni (J. G. Cooper). PI. X, figs. 18-22; PI. XI, fig. 28, 29, Pl. XIII, figs. 59-62; Pl. XVI, figs. 92, 93. Arion ? Andersonii J. G. Cooper, Proc. Acad. Nat. Sci., Phila., 1872, p. 148, pl. 3, f. F, 1-5. Not ‘‘Prophysaon Andersoni J, G. Cooper,” W. G. Binney, Second Supple- ment to T. M., V, p. 42 (=. fasciatum), Prophysaon Andersoni J. G. Cooper, W. G. Binney, Third Supplement to Terr. Moll., V, p. 208, pl. iii, f. 1, pl. vii, f. C; pl. i, f. 3 (dentition), pl. ix, f. 1, J (surface reticulation). Fourth Supplement, p. 179. : Prophysaon Andersoni J. G. Cooper, Proc. Amer. Philos. Soc., 1879, p. 288. Cockerell, Ann, Mag. N. H. (6), VI, R. 278; Nautilus XI, p. 77,78 (includes P, Hemphilli). Raymond, Nautilus LV, p. 6. : Prophysaon Andersoni yar. marmoratum Ckll., The Conchologist II, p, 72. P. Andersoni var, suffusum Ck\l., The Conchologist LI, p. 118. Prophysaon Hemphilli Bland & Binn., Ann. Lyc. N. H, of N. Y., X, p. 295, pl. xiii, exclusive of fig. 5 (external view, shell, jaw, teeth, digestive system and 246 PROCEEDINGS OF THE ACADEMY OF [1898. genitalia). W.G. Binney, Terrestr. Moll., V, p. 238, f. 137, 188, 139, pl. v f. 1 (teeth), = xii, f. H_ (genitalia), ‘‘specimens from Mendocino County’ excluded. Man. Amer. Land Shells, p. 105, f. 68, 69, 70. Third Supplement to T. M., V, p. 208, pl vii, f. D. Simroth, Nova Acta Acad. Cees. Leop.- Carol. Germ. Nat. Cur., LVI, 1891, p. 362, pl. 7, f. 5-8 (full account of anat- omy). Taylor, The Ottawa Naturalist ITI, p. 90. Prophysaon pacificum Cockerell, Nautilus III, p. 111 (Feb., 1890); V, p. 31; XI, p. 77 (includes favum). W. G. Binney, Third Supplement to T. Ne V, p- 210, pl. vii, f. B. F. H. Prophysaon flavum Cockerell, Nautilus ITI, p. 111. Ann. Mag. N. H. (6), at Pp: een as var. of pacificum. W.G. Binney, Third Suppl., p. 210, E Scabbiean Andersonii var. pallidum Ck\l., Nautilus V, p. 31. Length in alcohol 25-35 mm. Upper surface buff-gray or whit- ish flesh colored, with irregular blackish diamond venation and sometimes suffused with purplish-black, showing a pale dorsal line; the mantle yellowish, with two curved lateral black stripes, with or without scattered marbling; sole pale buff or dirty white ; foot-mar- gin pale; below and anterior to mantle whitish. Integument with rather coarse diamond venation, the areole subdivided into minute polygonal granules. Shel] oval, with moderately consistent calcareous layer. Genitalia (Pl. XIII, figs. 59, 60, 61): Epiphallus cylindric, straight or sometimes curved, with an abrupt basal constriction, kink and peduncle secured by a short muscle, as described above. Vas deferens very long, its length measured from end to the abrupt bend at the atrium being about 7 times the length of the epiphallus; thrown into a complicated snarl. Spermatheca globose or oval, on a rather slender duct. Vaginalong. Free oviduct short. Ovotestis showing externally a compact mass of rounded follicles. Right eye retractor passing between branches of genitalia. Measurements of several specimens are as follows: a (Mus. no. 69,010, Oakland, Cal.), length of swollen epiphallus 9 mm.; length of extended vas deferens, from apex of the epiphallus to base of same 64 mm.; b (same locality), epipballus 5, v. d. 36 mm.; ¢ (Port- land, Ore.) epiphallus 5.5, v. d. 37 mm. Jaw (Pl. XVI, fig. 92, specimen from San Juan I.) arcuate with about 15 well-defined ribs, denticulating the basal margin. Radula with 44-1-44 teeth; rachidian tricuspid, laterals bicuspid, the ectocones quite small; marginals with moderately long, pointed mesocones and minute ectocones (Pl. XVI, fig. 93, two outer lateral, and a group of marginal teeth). Alcoholic P. Andersoni varies in general tone from a smoky lead color above to reddish with black marbling or suffusion, mantle light 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 247 dirty buff, or yellow, variously marked. Very rarely the two curved black stripes on the mantle are wanting, and occasional specimens fail to show the pale dorsal line, which in others is very conspicuous. We fail, however, to find internal characters permit- ting the division of our series into several species; and while it is possible that some of the named forms may be geographic subspecies, we are disposed to regard them rather as local variations of but slight rank and uncertain diagnosis. Large series from many local- ities must be collected and compared to define the subspecies, if any exist. It differs chiefly from P. foliolatum in being smaller, with very ouch shorter “ amputateable ” tail segment, and in dentition. Simroth found a very long, smooth, vermiform spermatophore in P. Andersoni. Santa Clara Co. (Ebrhorn, Raymond) around San Francisco Bay (Cooper, Button, et a/.), California; Portland (Malone), Forest Grove and Astoria (Hemphill), Oregon; Kalama, Chehalis, Port Townsend and San Juan Island (Hemphill), Washington; Van- couver Island (Wickham, Taylor); Old Mission, Lake Ceeur d’Aléne, Idaho (Hemphill). There is considerable variation in the shape and size of the epi- phallus, even among specimens of similar size and external appear- ance, collected at the same time at one locality. Thus, in one spec- imen of a small series from San Juan Island, the epiphallus is 44 mm. long, and straight (fig. 61); while in another it measures 7 mm. and is curved (fig. 59). The extremes in a larger series from Oak- land, Cal., are: shortest, 5 mm. long, straight; longest 8 mm. long, curved. After vainly trying to correlate the variations of the epiphallus with other characters, with a view to defining two or more species, we are compelled to conclude that they are largely individ- ual, possibly to some extent functional, but that these variations are not in any sense characteristic of races or species. Of course the observations were made upon sexually mature individuals.” Of the several forms included in the above synonymy, it is now generally admitted that P. Hemphilli isa synonym of P. Andersoni. Professor Cockerell" has stated his opinion that P. flavum, described ‘TMr. Cockerell’s division of Propfhysaon into forms with the epiphallus “sausage-shaped”’ and those with it “ banana-shaped”’ is therefore not a spe- cific criterion according to our observations. * Nautilus, XI, p. 77, Nov., 1897. 248 PROCEEDINGS OF THE ACADEMY OF [1898. from Gray’s Harbor, Washington, is to be included in P. pacificum, There are all possible intergradations between the ochreous and grayish forms in P. Andersoni and P. foliolatum. In P. pacificum we fail to see any specific characters. The color- ation agrees well with specimens of undoubted P. Andersoni from Washington, and neither the measurements nor the dentition offer differential characters, so far as we can see. The types were col- lected by Mr. Wickham, near Victoria, Vancouver Island. P. foliolatum (Gould). PI. X, figs. 15, 16, 17; Pl. XI, fig. 32; Pl. XIII, figs. 55, 56, 57, 58; Pl. XIV, fig. 70; Pl. XV, fig. 80; Pl. XVI, figs. 90, 98. Arion foliolatus Gould, Moll. U. 8S. Expl. Exped., p. 2, Pl. I, f. 2a, b (1852); Binney, Terr. Moll, II, p. 30, Pl. 66, f. 2 (1851). Copied by subsequent writ- ers. W. G. Binney, Second Supplement to Terr. Moll., V, p. 206, PI. viii, ff AUB OPM ix ££ 8,O;.D. Phenacarion foliolatus Ckll., Nautilus., iii, p. 127 (March, 1890); Ann. Mag. N. H. (6), VI, pp. 278, 279; W. G. Binney, Fourth Supplement, p. 181. Arion foliatus W. G. Binney, Proc. Acad. Nat. Sci. Phila., 1858, p. 197. Arion foliolatus var. Hemphilli W. G. Binney, Third Supplement, T. M. V, p. 208, Pl. viii, f. C; ix, f. H (genitalia). Cockerell, Nautilus, III, p. 126 (March, 1890). Phenacarion Hemphilli W. G. Binney, Fourth Supplement to T. M. V, p. 183 (not Prophysaon Hemphilli Bld. & Binn.). Length (in alcohol) 50-80 mm. Rather slender, the posterior third (or more) often distinctly more attenuated, defined by an ob- lique groove. Mantle oblong, its length contained 23 to 3g times in the total length of body, the breathing orifice decidedly in front of the middle. Foot margin rather wide; wrinkles of the sole corres- ponding to vertical grooves of the foot margin, bending backward and meeting in the middle; pedal groove deep, with no noticeable caudal pore. Colors variable: (1) Back clear reddish-fawn with a lighter dor- sal band, sometimes obsolete, the mantle with the usual two curved black lateral stripes, with or without scattered maculz; becoming paler, light yellowish on the sides and sole; or (2) back reddish, suffused with black, mantle bands long, often with a third median band and scattered macule, foot with the principal veins of the reticulation black-pigmented, as are alternate grooves of the foot margin; sides paler, gray; sole yellowish. Surface with deeper oblique grooves connected by short longi- tudinal grooves to form a roughly diamond-shaped reticulation, the meshes of which are minutely subdivided. Shell very delicate, membranous, with a thin and incoherent. layer of calcareous granules. , = 6: Wiles: | sea nl J pwrenn 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 249 Jaw (Pl. XVI, fig. 98) strong, opaque, with 8-14 wide flattened ribs. Radula with 44-1-44 teeth. Centrals tricuspid, laterals bicus- pid, the ectocones small. Marginals formed by shortening of the basal-plates, having the mesocone short, ectocone simple or on some teeth bifid (Pl. XVI, fig. 90). Epiphallus stout, cylindric, curved, with the usual constriction, peduncle and muscle at base. Vas deferens extremely long, elabor- ately twisted and tangled. Vagina long, the spermatheca duct about as long as the spermatheca. Albumen gland very large, long and tongue-shaped. Ovo-testis a very compact mass showing exter- nally only the rounded-polygonal ends of the closely packed folli- cles. In two typical individuals from Seattle (Mus. no. 71,072) the measurements are: a (fig. 55), length of swollen epiphallus 12.5 mm., of extended vas deferens from summit of epiphallus to base of same 92 mm.; of albumen gland 28 mm.; length of animal 80 mm. b (fig. 57), length of epiphallus 14 mm.; of vas deferens 114 mm. The ratio of length of epiphallus to that of vas deferens as measured above is about 1:73 or 8. The original of fig. 58 is a small speci- men, perhaps not fully adult. Type locality, Discovery Harbor, Puget Sound (Pickering). Also occurs at Olympia (Hemphill), Seattle (Hemphill, Randolph), and doubtless throughout the Puget Sound region generally. P. foliolatum is very closely allied to P. Andersoni Coop. It is larger, more elongated, with the solid portion of the tail, or that sub- ject to amputation, longer in proportion than in Andersoni. In living specimens a mucous pore is visible at the tail, but this is not noticeable externally in alcoholic examples. The light dorsal line is occasionally indistinguishable. The jaw forms probably intergrade with P. Andersoni; but the teeth differ quite perceptibly in the shorter, blunter cusps of the outer laterals and inner marginals. This is one of the best specific characters. The form described by Binney as Phenacarion Hemphilli does not seem to offer sufficiently tangible points of difference from folio- latum to stand as a species,even were the name not preoccupied. It is said to be “more slender and more pointed at the tail than foliolatus. The body is a bright yellow with bluish-black reticula- tions. The edge of the foot and the foot itself are almost black. Shield irregularly mottled with fuscous. The body also is irregu- 17 250 PROCEEDINGS OF THE ACADEMY OF [1898. larly mottled with fuscous, and has one broad fuscous band down the center of the back, spreading as it joins the mantle, with a nar- rower band on each side of the body. It loses its color on being placed in spirits, becoming a uniform dull slate color. Mantle lengthened oval. Shell-plate represented by a group of calcareous grains concealed in the mantle ; it is impossible to remove it as one shell-plate. A decided caudal pore.” The jaw and dentition are as in foliolatum. Genitalia much as in foliolatum, but Binney found the albumen gland to be much shorter, less tongue-shaped and brown-tipped. The epiphallus tapers distally, instead of contract- ing abruptly. Localities: Gray’s Harbor and Chehalis, Washington. The only characters of importance are the dorsal band, which seems to be similar to P. fasciatum, and the tapering epiphallus, also a character of that species, if not, in this case, an indication of sex- ual immaturity. Mr. Cockerell considers it asynonym of foliolatum ; and, as we have seen no authentic specimen, and the name is, in any case, preoccupied, we consider it best to leave the form as a syno- nym of foliolatum, pending further information. In aseries from Cascade Springs, on the Columbia River near the Government locks, collected in October, 1897 by Mr. J. G. Malone, (P1. XIII, fig. 54) the epiphallus is shorter, not curved, the vas deferens also much shorter. The spermatheca is subglobular. Measurements: length of epiphallus 8.6 mm.; of extended vas deferens from apex of the epiphallus to the abrupt curve at base of same, 42 mm.; of albumen gland 13 mm.; length of animal 50 mm. As measured above, the epiphallus is about one-fifth the length of the vas deferens. In typical foliolatum it is about one-eighth, in Andersoni one-seventh. These specimens are (in alcohol) less ver- miform than typical foliolatum, with paler color, back including shield, reddish, fading on the sides; mantle striped as usual, but blackish stripes defining the dorsal pale stripe either very faint or lacking, so that in some individuals no pale dorsal line is visible. The jaw in this form (P]. XVI, fig. 89) resembles that of P. Ander- soni in the numerous ribs. Radula with long, pointed mesocones on outer lateral and inner marginal teeth, as in P. Andersoni. In typical P. foliolatus the corresponding teeth are shorter and blunter. This will probably prove to be a distinct subspecies, and re- ferable to P. Andersoni rather than to foliolatum. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 251 P. humile Cockerell. Pl. XVI, fig. 97. Prophysaon humile Cockerell, Nautilus, iii, p. 112 (February 1890), Ann. Mag. N. H. (6), VI, p. 277, 279. W.G. Binney, Third Suppi., p. 211, Pl. VU, figs. E, G, L, M. We do not consider P. humile” specifically distinct from fasciatum. The coloration, genitalia and teeth are practically identical, and the character of the jaw (PI. XVI, fig. 97) does not seem to be constant. Several specimens selected at random from our series of fasciatum from Seattle have a jaw neither plaited ur ribbed, but densely, irregularly striated. Wecannot find any other differences between these specimens and the ordinary fasciatum with flat-ribbed or plaited jaw. The name humile has precedence over fasciatum and if the two forms prove to be, as we think, specifically identical, fasciatum will be reduced to varietal rank. P. fasciatum Cockerell. PI. X, figs. 23-27; Pl. XI, fig. 34; Pl. XII, figs. 37-40; Pl. XVI, figs. 91, 94-96. Prophysaon fasciatum Cockerell in Binney, Third Supplement to Terr. Moll., V, p- 209, pl. vii, f. A (May, 1890). W. G. Binney, Fourth Supplement, p. 180, Cockerell, Ann. Mag. N. H. (6), VI; p. 278, 279. Prophysaon Hemphilli,** specimen from Mendocino County,” W. G. Binney, Terr. Moll., V, p. 239, pl. xii, f. I. Prophysaon Anderson J. G, C., W. G. Binney, Second Supplement, p. 42. Prophysaon fasciatum yar. obscurum Ck\l. The Conchologist II, p. 119 (Chehalis, Wash.) Length (in aleohol) 25-35 mm., rarely as much.as 50 mm. Gen- eral form and surface reticulation as in P. Andersoni. Color ex- tremely variable: (1) Whitish-buff, (2) bluish-gray, or (3) red on the back, gray-buff at the sides, always with two conspicuous black stripes (well- or ill-developed) along the sides behind the mantle, defining a wide, wedge-shaped light dorsal area, which encloses a 1° The original description is as follows: “ Prophysaon humile Cockerell— Length (in alcohol) 164 mill. Body above and mantle smoke-color, obscured by bands. Mantle wrinkled, and having a broad dorsal and two lateral black- ish bands, reducing the ground-color to two obscure pale subdorsal bands. Length of mantle 7 mill., breadth 5} mill. Respiratory orifice 2} mill. from anterior border. Body subcylindrical, somewhat tapering, rather blunt at end. Distance from posterior end of mantle to end of body 8 mill. Back with a blackish band reaching a little more than half its length, and lateral darker blackish bands reaching its whole length. Keticulations distinct “foliated.” Sole strongly transversely striate-grooved, but not differentiated into tracts. Jaw pale, strongly striate, moderately curved, not ribbed, Lin- om membrane long and narrow. Teeth about 35-1-35. Centrals tricuspid, aterals bicuspid, marginals with a large point, and one (sometimes two) small outer points. Liver pale chocolate. Found by Mr, A. F. Wickham under the bark of rotten logs in the woods around Lake Coeur d’Alene, Idaho, 1889. In its reticulations and general characters this species resembles P. Ander- soni, of which it is possibly a variety.” 252 PROCEEDINGS OF THE ACADEMY OF [1898. similarly shaped dark stripe running backward from the mantle, sometimes well-defined, sometimes faint. Mantle buff or red, with two curved lateral black bands (sometimes obsolete) and scattered black maculation or marbling. Shell rectangularly oblong, 2 or 3 mm. long. Epiphallus slender, long, and tapering distally, having an abrupt kink at base, secured by a short muscle, as usual in the genus. Vas deferens neither lengthened nor convoluted. Vagina apparently functional asa penis. Spermatheca globose or oval, on a short, stout duct which is directly continued into the vagina. Free oviduct short and slender. Ovo-testis a rather loose bunch of oval follicles (fig. 38).. Albumen gland unusually hard and brittle. The right eye retractor passes between the branches of genitalia. In one specimen (Pl. XII, fig. 57) there seems to be a glandular enlargement of one side of the base of the epiphallus with a small tubercle on the other side. This may be pathologic. Jaw (Pl. XVI, figs. 94-96) arcuate with a slight median projec- tion below, covered with flat, narrow, crowded ribs separated by very narrow, shallow intervals, or with flat, slightly imbricated plaits (or merely densely, irregularly striated vertically in form humile, see above.) Radula with 35-1-35 teeth. Centrals tricuspid; laterals lacking the entocone; marginals formed by union of ectocone with mesocone and shortening of the basal-plate. The cusps are short throughout. The change from laterals to marginals is so gradual that it is prac- tically impossible to draw a line between them. On some outer marginals the ectocone is bifid. The figure shows a central with one lateral and a group of three inner marginals. Well and constantly distinguished from P. Andersoni ian folio- latum externally by the wide, light dorsal area enclosing a darker median stripe, and bounded laterally by blackish bands. Inter- nally, the slender, tapering epiphallus and short vas deferens are even more characteristic. The scarlet color of the back, noticed by Cockerell in some specimens, is not accidental, but of common occur- rence. In form the species varies (in alcohol) from a long, vermiform shape to about the contour of P. Andersont. The body-cavity extends nearly to the end of the tail. Self- excision of the tail occurs, but the amputated portion is short, as in P. Andersoni, and the great majority of individuals we have seen show no oblique constriction of the tail. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 253 P. coeruleum Cockerell. Pl. IX, figs. 7-11; Pl. XI, fig. 30; Pl. XIII, figs. 51-53 ; PI. XVI, fig. 86. Prophysaon coeruleum Cockerell, Nautilus, iii, p. 112, Ann. Mag. N. H. re VI, p. 278. -W. G. Binney, Third Suppl. T. M. V, p. 209, Pl. vii, f. bis P. coeruleum var. dubium Ckll., 7. c.; W.G. Binney, Z. c. Length (in alcohol) about 15 mm.; color blue or slate-blue (some- times brown), somewhat paler at the sides. Back with close, deep longitudinal grooves, which, on the sides, become oblique and more spaced, and more anteriorly they radiate vertically below the man- tle ; transverse grooves uniting the longitudinals comparatively few and shallow. Foot-margin very narrow, a second narrow well- defined sub-margin above it. Tail without caudal pore, frequently self-amputated and leaving a conspicuous longitudinal slit (Pl. LX, fig. 7, and figs. 9-11, the excised portion).” Genitalia (Pl. XIII, fig. 51-53) somewhat as in P. Andersoni. The epiphallus is short ; in one of the original specimens from Olym- pia (Pl. XIII, figs. 52, 53) very short, truncated at the ends; in another specimen from Seattle (Pl. XIII, fig. 51) itis oblong; vas deferens tangled, but shorter than in Andersoni. Spermatheca globular, on a rather slender duct, which is short in the Olympian specimen, longer in that from Seattle. Radula about as in P. fasciatum; the cusps of outer lateral and inner marginal teeth rather short; marginals quite wide (Pl. XVI, fig. 86). Type locality, Olympia, Washington (Hemphill). In addition to part of Hemphill’s original lot, we have received it from Seattle (P. B. Randolph) and Portland, Oregon (J.G. Malone). Mr. Ran- dolph writes that “it occurs solitary in dark fir woods under damp logs. Color in life a brighter shade of blue. They do not bear handling.” “P. ceruleum is an exceedingly distinct species, distinguished at once by its color and the character of its reticulations.” In the lat- ter respect, the species differs from all others of the genus, and re- - ©The original description from larger specimens than we have seen, is as fol- lows: ‘“‘ Length in (alcohol) 224 mill., in motion 43 mill. Body and mantle clear blue-gray, paler at sides, sole white. Mantle finely granulated, broad, without markings. Length of mantle 7 mill., breadth 5 mill. Respirator orifice 2} mill. from anterior border. Body subcylindrical, tapering, tps | (In one specimen eaten off at the end.) Distance from posterior end of man- tle to end of body 10} mill. The reticulations take the form of longitudinal equidistant lines, occasionally joined by transverse lines, or coalescing. Sole not differentiated into tracts. Jaw pale, strongly ribbed. Liver white. Mr. Binney sends me colored drawings of the living animal; the neck is long and white, or very pale.” 254 PROCEEDINGS OF THE ACADEMY OF [1898. sembles Ariolimax. The very narrow foot-margin, with an unusu- ally distinct border above, is another distinguishing feature. Most of the specimens we have seen have lost the end of the tail by self-amputation, as shown in the figures. When perfect the tail is pointed, with no perceptible mucous pore; the longitudinal grooves of the back become irregular near the end of the tail. The color of Portland and Seattle specimens is distinctly blue, but some of the original lot from Olympia, collected about eight years ago, have become brown. Mr. Cockerell thus describes a variegated form which he refers to cerulewm as a variety :— “Prophysaon ceruleum var. dubium. Length (in alcohol) 8 mill. Length of mantle, 4 mill. Distance from posterior end of mantle to end of body 34 mill. Mantle broad, with four bands composed of coalesced black marbling, very irregular in shape, and running together anteriorly. Body dark, tapering. Sole pale, its edges gray. Liverwhite. With the P. ceruleum isa small dark slug, prob- ably a variety of it, but differing as described above. It will easily be distinguished by its blackish color and the peculiar markings on the mantle.” There are, in some specimens, very close, fine, superficial im- pressed vertical lines crossing the deeper oblique grooves. Genus ANADENULUS Cockerell, 1890. Anadenulus Ckll., Ann. Mag. N. H. (6), VI, p. 279 (Oct., 1890). Slugs with the minute, non-spiral shell plate wholly buried; the mantle small, rounded and anterior, with breathing pore median on the right side. Genital orifice below right tentacle. Foot reticu- late, somewhat keeled posteriorly, the foot-margin moderate, pedal grooves rising slightly at tail, with no caudal pore there; sole dis- tinctly tripartite, the areas separated by longitudinal grooves, mid- dle field narrower than side fields (P]. IX, fig. 12). Body-cavity extending the entire length. Jaw with about 20 wide, flat ribs (Binney). Radula with 20-1-20 teeth, about as in -rophysaon in form. Intestinal tract (Pl. XI, fig. 35) much as in Prophysaon ; posterior loop formed by G* and G* extending far behind that formed by G' and G’, slightly twisted posteriorly, the folds elsewhere hardly twisted. Genital system unknown. Muscle system (Pl. XIV, fig. 68) as in Prophysaon. Eye retract- ors inserted at the two posterior angles of the diaphragm, the buc- 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 255 cal retractor at the posterior margin somewhat to the right of the median line, shortly bifurcate distally. Pallial region (PI. XV, fig. 75). Kidney large, rounded nearly filling the lung cavity. Ventricle exposed. Distribution: San Diego Co., California. No adequate discussion of the affinities of Anadenulus can be en- tered upon until well-preserved specimens are collected permit- ting an examination of the genitalia. Present information indicates its proximity to Prophysaon, with which Anadenulus agrees in the di- gestive tract and musculature. But the voluminous kidney, exposing only the ventricle, the conspicuously tripartite sole, and the appar- ent absence of that peculiar structure of the tail which distinguishes Prophysaon, are all important characters indicating the distinctness of the two genera. Turning to Old World genera, we find Arion differing in its tail gland, posteriorly prolonged buccal retractor and complexly twisted intestine. Geomalacus shows the same with still other differences ; and in Anadenus the foot margin is very much narrower, the sole not divided by longitudinal grooves, and the intestine is long and spirally twisted. A. Cockerelli (Hemphill). Pl. IX, figs. 12, 13, 14; Pi. XI, fig. 35; Pl. XIV, fig. 68; PI. XV, fig. 75. Anadenus Cockerelli Hemphill, Nautilus, [V, p. 2 (May, 1890), W.G. Bin- ney, Fourth Supplement to Terr. Moll.,V, p. 178, Pl. i, f. 1; Pl, iii, f. 5 (den- gaia has Cockerelli Cockerell, Ann. Mag. N. H. (6), VI, p. 278, 279 (Oct., 1890). Alcoholic specimens have the foot blackish, with a short, light stripe behind the mantle above, the sides below mantle and the head pale; mantle small, short, black with two festooned longitudinal yellowish stripes. Length 9-134 mm. Cuyamaca Mts., San Diego Co., California (Hemphill). IV. BRIEF DIRECTIONS FOR COLLECTING, PRESERVING AND EXAMINING SLUGS.” In the Northern States the best time for collecting slugs 1s in early spring. From February to July, most well grown specimens As many of our American conchologists have not ‘collected or studied slugs especially, we have thought it not superfluous to append the following notes on collecting slugs, with rough directions for their examination. It will readily be understood that if the slug to be examined is of very small size, or it is necessary to obtain all the data from one or two specimens, more or less radical] modifications of these instructions must be made. 256 PROCEEDINGS OF THE ACADEMY OF [1898. taken will prove to have the reproductive organs fully developed. Autumn and late summer are a somewhat less favorable time, be- cause the young of the year have then attained the full growth of the species, while upon opening them the genitalia are found un- developed. Still, autumn specimens should be collected. Always date each “catch” and keep it separate.” The best preservative for slugs (and other land mollusks) is alco- hol. Of other preservatives, formalin (formaldehyde) is perhaps the best; but it is, on the whole, a very unsatisfactory substitute, ren- dering the tissues tough and slippery, difficult to dissect, and gener- ally destroying calcareous organs in time. Formalin specimens are, moreover, inferior to alcoholic for histological study. Upon the whole, then, formalin should only be used as a permanent preserva- tive for large slugs, if at all, and then in a three or four p. ec. solu- tion. It should be added, however, that when travelling with limited. means of conveyance, it is often convenient to use formalin on ac- count of the economy of carrying it in the commercial strength, to be diluted as occasion arises. Never crowd snails in formalin; the bulk of the solution should exceed that of the snails six or eight times. After collecting slugs they should be drowned by placing in a vessel of water with a lid laid on (not a cork pushed in) to exclude air. Generally twelve hours is a sufficient time, but this depends upon the slugs and the temperature. In hot weather less time is required. Test them by taking one out, touching it with alcohol, and if no retraction takes place they are ready to be transferred to 25% alcohol; leave in this about twelve hours, then transfer to 50%, and after twenty-four hours or more to about 75%, in which they may be permanently kept. If formalin is used, the slugs may be placed in the 3 or 4% solu- tion when drowned, and changed to fresh solution after a few days, the first being thrown away. Formalin specimens may at any time be transferred to alcohol, or it may be used with asmall per cent. of alcohol. 22 Of course, for economy of space and alcohol, all the lots of one species may be kept in one jar, each in a separate vial or piece of cheese-cloth. 2 Of course, in field work the exact proportion is not vital. In general, it is best to use a mixture of three parts of water to one of alcohol at first, then a half and half mixture, and then the permanent strength. ‘The first and second mixtures may be kept and used repeatedly, occasionally adding a little alcohol to keep up the strength. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 257 To dissect slugs use a small pan, say 4x6x1} inches, with a layer of blackened wax on the bottom. Only a pair of fine scissors, a pair of fine-pointed tweezers, a small scalpel and a supply of fine pins, with, of course, the small lens usually carried by naturalists, is necessary. Cut the outer integument across the head and along the left side, pin sole down in the pan, with water enough to cover, open by turning the dorsal integument to the right, and cut the rectum where it enters the back. The digestive tract may then be studied by picking away the liver, and, with ordinary care, the genitalia may be removed and isolated by cutting out a small area around the genital orifice. After observing its insertion, the penis retractor may be cut. If specimens are abundant, use another for the examination of the muscles and pallial organs. Open by cutting just above the foot groove all around the body; remove the sole, pin back downward in the dissecting pan and remove the digestive and genital systems, care being taken to break no muscles. The whole retractor system will then be seen, and after study the muscles may be cut and the diaphragm carefully removed, disclosing the kidney, heart and lung, as seen in the figures on Plate XV. Use a large slug to begin with,such as Limax maximus, the Ario- limaces or Aphallarion, and no difficulty not readily overcome will be encountered. BIBLIOGRAPHY. References cited under the several genera and species comprise all or nearly all writings upon American Arionidz, A catalogue of the foreign papers con- sulted in our studies would unnecessarily extend this article, as the literature is given almost in full in one or other of the following papers, which we have found of especial use. Gopwin-AusTeNn, H. H. Land and Freshwater Mollusca of India, Pt. I, pp. 46-65 (1882). SimrotH, H. Versuch einer Naturgeschichte der deutschen Nacht- schnecken und ihrer europiiischen Verwandten. Zeitschr. f. wissensch. Zool., 1885, pp. 203-366. Bibliography on pp. 359-361. SmmrortuH, i Beitriige zur Kenntniss der Nachtschnecken. Nova Acta k. Leop.-Carol. deutschen Akad. Wissensch., LIV, No. 1, pp. 1-91 (1889). Scuarre, R. F. The slugs of Ireland. Sci. Trans. Roy. Dublin Society, IV, Ser. 2, pp. 513-562. Bibliography, pp. 557, 558 (1891). SmmrotH, H, Die Nachtschnecken der portugesisch-azorischen Fauna, Nova Acta, ete., LVI, pp. 201-424 (1891). Bibliography on pp. 416-419. CocKERELL, T. D, A. Check-List of Slugs. The Conchologist II, p. 158. Cotitince, W. E. On some European Slugs of the Genus Avion. Proce. Zool. Soc. London, 1897, p. 439. 258 PROCEEDINGS OF THE ACADEMY OF [1898. DESCRIPTION OF PLATES. Prats IX, Figs. 1,2. Hemphillia glandulosa Bld. & Binn. Dorsal outline and lateral aspect of a specimen from Astoria, Oregon (Hemp- 0 Ra Mus. no, 71,161. m, mantle; sh, exposed surface of shell. Figs. 3,4. Hemphillia camelus Pils. & Van. Lateral and dorsal aspects of the type specimen. Old Mission, Idaho. Mus. no, 63,926. Figs. 5,6. Hesperarion niger (J. G.Coop.). Ventral and lateral aspects of a maculated individual. Santa Clara, Cal. Mus. no. 71,198. Figs. 7, 8. Prophysaon ceruleum Ckll. Dorsal and lateral aspects of a specimen which has lost its tail by self-amputation. Olym- pia, Washington. Mus. no. 63,913. Figs. 9,10, 11. Prophysaon ceruleum Ckll. Lateral, anterior and dorsal aspects of the self-amputated tail of a specimen from Seattle, Washington. No. 71,074. Figs. 12, 13,14. Anadenulus Cockerelli (Hemph.). Ventral, lat- eral and dorsal aspects of one of the original specimens, from Julian City, San Diego Co., California. Mus. no. 63,895. PLATE X. Figs. 15,16. Prophysaon foliolatus (Gld.). Lateral and dorsal views of a typical specimen from Seattle, Washington. Mus. no. 71,072. Fig. 17. Prophysaon foliolatus (Gld.) Same specimen, the mantle turned backward to show position of its anterior insertion. Figs. 18, 19. Prophysaon Andersoni (J. G. Coop.). Oakland, California. Mus. no. 69,010a. Figs. 20, 21,22. Prophysaon Andersoni (J. G. Coop.), San Juan Island, Washington. Mus. no. 63,912. Figs. 23, 24. Prophysaon fasciatum Ckll. Seattle, Washington. Collected in March or April, 1896. Mus. no. 68,025. Figs. 25,26. Prophysaon fasciatum Ckll. Lateral views of two individuals from Seattle, Washington. Fig. 27. Prophysaon fasciatum Ckll. Same individual as fig. 26, with mantle turned backward to show position of its anterior insertion. Pratze XI. [All figures represent the digestive tract viewed from above. A. gl., albumen gland; B. d., bile duct; B. m., buccal mass; G', first, second, third and fourth folds of the gut; Gen. or., exter- ‘nal genital orifice; ZL, liver; 0. t., ovo-testis ; sp., spermatheca ; T, tail; wt., uterus; vag. vagina. | 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 259 Fig. i Prophysaon Andersoni (Coop.). Oakland, Cal. Mus. no. 9,010a. Fig. 29. Prophysaon Andersoni (Coop.). California. Mus -no, 71,071. Received from W. G. Binney as P. Hemphilli B. & B Fig. 30. Prophysaon eeruleum Ckll. Fig. 31. Binneya notabilis Cooper. Guadalupe Island. Mus. no. » . 71,923. Fig. 32. Prophysaon foliolatum (Gld.). Seattle, Wash. Fig. 33. Hesperarion niger (Cooper). California. Mus. no. 71,- O78. o.t., ovo-testis; L, liver, 7, tail. Fig. 34. Prophysaon fasciatum Ckll. Seattle, Wash. Mus. no. 68,026. Salivary glands and anterior portion of liver removed, genitalia and digestive tract in situ. Fig. 35. Anadenulus Cockerelli (Hemphill). One of the original lot. Fig. 36. Hemphillia camelus Pils. & Van. Old Mission, Idaho. Mus. no. 63,926. 0. t., ovo-testis. PuaTeE XII. [Epi., epiphallus; p. p., penis papilla; r. p. penis retractor; v. d., vas deferens ]. Fig. 37. Prophysaon fasciatum Ckll. Seattle, Wash. Mus. no. 68,026a. Perhaps abnormal. Fig. 38. Prophysaon fasciatum Ckll. Same locality. Ovo-testis. Fig. 39. Prophysaon fasciatum Ckll. Same locality. Mus. no. 68,025, Fig. 40. Same specimen, atrium and base of the epiphallus, the binding muscle removed. Fig. 41. Hemphillia camelus Pils. & Van. Type specimen. Maus. no. 63,926, Fig. 42. The same, penis opened. Fig. 43. Hesperarion niger (Cooper). Spermatophore. Fig. 44. Hesperarion niger (Cooper). Santa Clara, Cal., collected Nov. or Dec., 1896. Fig. 45. Hesperarion niger (Cooper). Mus. no, 71,078. Apex of penis opened. Fig. 46. The same, side view of penis-papilla. Fig. 47. Hesperarion niger (Cooper). Mus. no, 71,077. Fig. 48. The same. Spermatheca. Fig. 49. Hemphillia grandulosa B. & B. Apex of penis opened, showing papilla. Fig. 50. Hemphillia glandulosa B. & B. Lower portion of genital system. Astoria, Oregon. Piate XIII. [f. ov., free oviduct ; muse., muscle connecting atrium and epiphal- lus ; sp., sp. d., spermatheca and its duct; vag., vagina; ped., peduncle of the epiphallus. } 260 PROCEEDINGS OF THE ACADEMY OF [1898. Fig. 51. Prophysaon eoeruleum Ckll. Seattle, Washington. Figs. 52, 538. Prophysaon coeruleum Ckll. Olympia, Washington. The pedicel of epiphallus is seen in fig. 53. Fig. 54. Prophysaon Andersoni (?) var. Cascade Springs, Wash- ington. Mus. no. 71,647. Fig. 55. Prophysaon foliolatum (Gld.). Seattle, Washington. Mus. no. 71,072. Typical form. Fig. 56. Thesame. Median transverse section of the epiphallus. Fig. 57. Prophysaon foliolatum (Gld.). Another specimen from the same locality. Fig. 58. The same, a smaller specimen not mature. Fig. 59. Prophysaon Andersoni (Cooper). Oakland, Cal. Mus. no. 69,010. Fig. 60. Prophysaon Andersoni (Cooper). California. Mus. No. 71,071. Received from W.G. Binney as P. Hemphilli B. & B. Fig. 61. Prophysaon Andersoni (Cooper). Oakland, Cal. Mus. no. 69,010. Fig. 62. Prophysaon Andersoni (Cooper). Spermatophore. PuaTE XIV. [The retractor muscle systems are all represented as seen from be- neath. ao, aorta; ¢. a., cephalic artery ; e. r., eye retractor; G, intestine; J. t. r., left tentacle and eye retractor; ovid. r., re- tractor of the oviduct; p, penis; ph.r, pharynx or buccal re- tractor ; ret., retensor muscle; 7. p., penis retractor; r. s., rad- ula sack ; r.¢. 7., right tentacle retractor ; sp.r, retractor of the spermatheca; t.r, tentacle retractor; vag., vagina; vag. 7., va- ginal retractor; v.a, visceral artery. | Figs. 63, 64,65. Binneya notabilis Cooper. Guadalupe Island. Ventral and lateral aspects of an alcoholic specimen, and the retractor system. Fig. 66. Arivlimax Columbianus (Gld.). Fig. 67. Aphallarion Buttoni Pils. & Van. Fig. 68. Anadenulus Cockerelli (Hemph.). Fig. 69. Hemphillia camelus Pils. & Van. Mus. no. 63,926. Fig. 70. Prophysaon foliolatum (Gld.). Mus. no. 71,073. Fig. 71. Hesperarion niger (Cooper). Mus. no. 71,078. Fig. 72. Arion hortensis Fér. Seattle, Wash. Mus. no. 68,023. PLatTE XV. [Pallial organs, seen from below, the diaphragm removed. a, auri- cle; ao, aorta; k, kidney; 7, lung; p.a., pulmonary or breath- ing aperture; ph.7., pharynx or buccal retractor muscle; p. v, pulmonary vein; 7, G*, rectum ; 7. t. 7, right tentacle retractor ; ur, secondary ureter; v, ventricle. | Fig. 73. Ariolimax Columbianus (Gld.). Maculated specimen from near Oakland, California. Pallial region from below, with pulmonary net work of the lung roof. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 261 Fig. 74. The same, showing main ramifications of excretory canals in kidney. Fig. 75. Anadenulus Cockerellii (Hemp.). Fig. 76. Aphallarion Buttoni Pils. & Van. Fig. 77. Hesperarion niger (J. G. Coop.). Mus. no. 71,078. Fig. 78. Hemphillia camelus Pils. & Van. Fig. 79. Arion hortensis Fér. Specimen from Seattle, Wash. Mus. no. 68,023. Fig. 80. Prophysaon foliolatum (Gld.). Specimen from Seattle. Wash. Mus. no. 71,073. Fig. 81. Ariolimax columbianus (Gld.) End of tail, lateral view. Figs. 82, 83. Arion hortensis Fér. Seattle, Washington. Fig. 84. Hesperarion niger (Coop.). Oblique view of end of tail, showing pore. PLATE XVI. Fig. 85. Hemphillia camelus Pils. & Van. Central, first lateral, and three marginal teeth. Fig. 86. so Si oy ceruleum Ckll. Group of outermost marginal teeth. Fig. 87. Binneya notabilis Coop. Jaw. Fig. 88. Binneya notabilis Coop. Teeth. Fig. 89. Prophysaon Andersoni (Coop.), var.? Mus. no. 71,647. Cascade Springs, Washington. Fig. 90. Prophysaon foliolatum (Gld.). Typical form. Central, first lateral, and group of marginal teeth. Fig. 91. Prophysaon fasciatum Ckll. Central, first lateral and group of marginal teeth. Fig. 92. Prophysaon Andersoni (Coop.). Jaw. San Juan Island. Mus. no. 63,912. Fig. 93. Outer marginal and lateral teeth of same individual. Fig. 94. Prophysaon fasciatum Ckll. Jaw. Mus. no. 68,026. Seattle, Washington. Fig. 95. Much magnified portion from median part of another similar jaw of the same species. Fig. 96. More enlarged basal margin of same. Fig. 97. Prophysaon humile Ckll. Much magnified portion of the basal margin of a striated jaw. Seattle, Washington. Fig. 98. Prophysaon foliolatum (Gld.). Jaw. Mus. no. 71,072. Seattle, Washington. 262 PROCEEDINGS OF THE ACADEMY OF [1898. May 3. The President, SAmuEL G. Drxon, M. D., in the Chair. Fifty-three persons present. Papers under the following titles were presented for publication :— “Notes on Mr. Meehan’s paper on the Plants of Lewis and Clark’s Expedition across the Continent, 1804-06.” By Dr. Elliott Coues. “List of Bats collected by Dr. W. S. Abbott in Siam.” By Gerrit S. Miller, Jr. May 10. The President, SAmMuEL G. Drxon, M. D., in the Chair. Twenty-six persons present. ; Papers under the following titles were presented for publication :— “Certain Aboriginal Mounds of the South Carolina Coast.” By Clarence B. Moore. “Certain Aboriginal Mounds of the Savannah River.” By Clarence B. Moore. “Certain Aboriginal Mounds of the Altamaha River.” By Clarence B. Moore. “Recent Acquisitions.” By Clarence B. Moore. “ Environmental and Sexual Dimorphism in Crepidula.” By E. G. Conklin. , May 17. Mr. Caarves P. Peror in the Chair. Thirty-six persons present. Papers under the following titles were presented for publication :— “Descriptions of five New Phyllostome Bats.” By Gerritt S. Miller, Jr. “Chitons collected by Dr. Harold Heath at Pacific Grove, near Monterey, Cal.” By H. A. Pilsbry. “Some New Species of Diatoms.” By C. S. Boyer. The deaths of Theodore Wernwag, May ist, and of J. Waln Vaux, May 16th, members were announced. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 263 May 24. The President, SAmvuEL G. Drxon, M. D., in the Chair. Forty persons present. Mr. CHAarLes Morris read a paper on the antiquity of Man from the standpoint of evolution. (No abstract). May 31. The President, SAamueL G. Drxon, M. D., in the Chair. Twenty-one persons present. A paper entitled “ Botanical Observations on the Mexican Flora, especially on the Flora of the Valley of Mexico.” By J. W. Harshberger, M. D., was presented for publication. Papers under the following titles were accepted for publication in the Journal :— ~ “Certain Aboriginal Mounds of the South Carolina Coast.” By Clarence B. Moore. “Certain Aboriginal Mounds of the Savannah River.” By Clarence B. Moore. “Certain Aboriginal Mounds of the Altamaha River.’ By Clarence B. Moore. “ Recent Acquisitions.” By Clarence B. Moore. The following were ordered to be printed :— 264 PROCEEDINGS OF THE ACADEMY OF [1898. MATERIALS TOWARD A NATURAL CLASSIFICATION OF THE CYLIN- DRELLOID SNAILS. BY HENRY A. PIISBRY AND E. G. VANATTA., While recording some recent additions to the North American landsnail fauna with the intention of revising the ‘‘ Check List ” of United States land mollusks published in these Proceedings for 1889, the attention of the senior author was recalled to the rejection of the generic name Cylindrella by Messrs. Harris and Burrows in 1891, and their substitution of a new name for the group. Upon compiling a list of the generic and subgeneric names which have been applied to species of “Cylindrella,” it became obvious that a thorough taxonomic revision was urgently needed. In order to as-, certain which of the numerous names should be retained as valid, to place these upon a solid basis, and to reduce the remainder to synonyms, it was found necessary to supplement a review of the lit- erature of the group by an examination of the snails themselves, especially with reference to the radulz, and the internal characters of the shells, revealed by a study of sections cut to expose the inter- nal columella or axis. This detailed examination has been made chiefly by the junior author of this paper. The characters of the radula have been utilized as a basis for classification by Crosse and Fischer in 1870, their paper marking an epoch in the taxonomic history of this family. W.G. Binney has added to our knowledge of this subject upon the lines laid down by the French writers ; and later, Strebel and Pfeffer, in their sug- gestive and original series of papers upon the Mexican fauna, have made important contributions toward a rational classification of the group. There are many other writings bearing upon the nomen- clature of the Cylindrellas, but no others of importance for original facts or views concerning their phylogeny or structure, aside from mere species work. The external conchologic characters of the Cylindrellas are well known by the writings of Pfeiffer, Poey and others, but the modifi- cations of the internal armature have been far less fully elucidated. A portion of Pfeiffer’s descriptions mention briefly the internal structure, and some ef the plates of the Novitates Conchologice 1898.] NATURAL SCIENCES OF PHILADELPHIA. 265 and Malakozoologische Blitter represent it; and Arango, in his Contribucion a la Fauna Malacologiea Cubana, notes the internal structure of the Cuban species. Most of these observations, how- ever, are not sufficiently detailed or exact to meet the requirements of the case, now that a classification is based largely upon internal structure ; and our own work is therefore founded wholly upon the study of a series of sections including nearly every species in the collection of the Academy. Without entering into any elaborate exposé or criticism of the work of former authors upon the Cylindrellas, attention should be directed to the contention of Crosse & Fischer’ and later of Fischer? that the series should be distributed between two family groups, the Cylindrellide and the Pupide, a conclusion based wholly upon the structure of the teeth and jaws; the first family having greatly mod- ified teeth and plaited jaw, the second having normal dentition and solid jaw. That this splitting of the Cylindrellas into two is an unnatural division, seems to us to be proven by the following considerations: (1) The discovery of completely Cylindrelloid shells (Epirobia) with the “‘normal” type of teeth. (2) The presence of transition stages in the teeth in the genus Holospira, and (3) the recent dem- onstration by the senior author of this paper’ of the rapid changes undergone by the teeth of some genera under the stress of changed habits, without corresponding changes in the rest of the anatomy, as seen in Papuina, Polymita, etc. (4) The general law of change in the structure of the jaw, as illustrated in the families Endodon- tide and Helicide, must now be recognized as largely discounting the old value placed upon that organ as a factor in systematic mal- acology ; and in any family of snails we may expect to find both the more primitive plaited and the later solid type of jaw. The final reason for rejecting the idea that any of the group under con- sideration are Pupida, is that none of them, so far as known, possess the extremely characteristic complication of the male genital organs found in Pupa, Buliminus, Clausilia, and their immediate allies, and which constitute one of the most important characters of the family Pupide. 1 Journ. de Conchyl., 1870. ? Manuel de Conchyliologie. * Manual of Conchology (2), LX, introduction and portions relating to ar- boreal Helices. 18 266 PROCEEDINGS OF THE ACADEMY OF [1898. Our further observations upon the family may be grouped under five heads :— I. Names applied to generic and minor groups of Cylindrelloid snails, II. Key to the genera and subgenera. III. Classified lists of the species with zoo-geographic and other notes. IV. Brief sketch of other genera of the family. V. Provisional phylogenetic diagram and table of geographic dis- tribution. I. CHRONOLOGICAL LIST OF NAMES APPLIED TO CYLINDRELLOID SNAILS. (Exclusive of those pertaining to Lia, Macroceramus, Holospira, and other generally recognized genera). 1822 (or earlier). CocuLopina Férussac, Tableau Systematique, etc., p. 24, 61. Under Helix, Férussac establishes a “ Quatorziéme sous-genre. Cochlodine, Cochlodina nobis.” The subgeneric definition applies better to Clausilia than to the other forms included by Férussac in the group; and, indeed, seems to be based wholly upon that genus. The species of Coehlodina are classified as follows :— * Shell dextral. + Aperture without teeth or lamin. 1. Peristome not continuous. Premier groupe. Les Pupoides, Pupoides. 493 carinata Gmel. [==Macroceramus lineatus Brug.]. 494 nebulosa nobis. [nomen nudum]. 495 ignifera nobis, [nomen nudum]. 2. Peristome continuous. Deuxiéme groupe. Les Trachéloides, Tracheloides. 496 sloanii nobis. [nomen nudum]. 497 draparnaldi nobis. [nomen nudum]. 498 petiveriana nobis. [probably—=C. eximia Pfr. ]. 499 blainvilliana nobis. [nomen nudum]. 500 cylindrus Chemn. [= Cylindrella]. 501 rosata nobis. [nomen nudum]. 502 truncata Dillw. [Undeterminable ?—=Megalomastoma]. 503 fasciata Lam. [ Undeterminable ?—=Megalomastoma]. Gar 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 267 504 tortuosa Chemn. [= Tortulosa tortuosa, an oriental operculate). 505 gracilicollis nobis. [nomen nudum]. 506 perplicata nobis. [nomen nudum]. 507 collaris nobis. [= Cylindrella]. 508 subula nobis. [nomen nudum]. 509 antiperversa nobis. [nomen nudum]. s +t Aperture armed with large folds or long teeth. 510 gargantua nobis [nomen nudum= Odontostomus]. ** Shell sinistral. 1. Aperture without lamine. Troisiéme groupe. Les Anomales, Anomales; Pupa Drap. 511 perversa L. [=Balea]. 512 chemnitziana nobis. [ Cylindrella elongata Chemn. ]. 2. Aperture armed (with laminz or an elastic operculum). Quatriéme groupe. Les Clausilies, Clausiliv ; genre clausilie Drap. [Includes the species of Clausilia, with some nomina nuda per- haps pertaining to other groups]. It will be seen that Cochlodina is a miscellaneous group, including species of at least six modern genera, all of which have since been named. Under these circumstances it had better be left as a synonym of Clausilia, as the diagnosis precludes its use for any of the other groups included. 1828. Bracuyrus Guilding, Zool. Journal, III, p. 167. Pro- posed for B. costatus Gldg. Preoecupied in Aves by Swainson, 1824, and in Diptera by Meigen in the same year. 1837. Urocortis Beck, Index Moll., p. 83. Species, petiverana Fér., blainvilliana Fér., eylindrus Ch., Dw. and Wood; rosata Fér., glandula B., abbreviata B., coarctata B., List H., XX1,17; trunea- tula Lam. (Clausilia), gracilicollis Fér. J. E. Gray, in Proce. Zool. Soc. Lond., 1847, p- 177, selects “Turbo” cylindrus as type. This would make the group equivalent to Thaumasia Alb. a later name. Von Martens, in Die Heliceen, 1860, names decollata Nyst as type. This species belongs to Crosse and Fischer’s later group Eucalodium ; and as it does not appear in Beck’s original list of species, must be rejected from the group. + Urocoptis is the earliest tenable name for any genus of the family. 1837. BracnyropeLia Beck, Index Moll., p. 89. Proposed for perplicata Fér., collaris Lam., subula Fér., antiperversa Fér. 268 PROCEEDINGS OF THE ACADEMY OF [18)8. 1837. Aroma Beck, Index Moll. p. 89. For elongata Chetan. (chemnitziana Fér.). Gray, 1847, and Morch, 1852, retain the name for this species. 1840. CyLInDRELLA Pfeiffer, Archiv fiir Naturg., p. 41. For the following species: Gracilicollis Fér. [a Brachypodella] collaris Lam, [a Brachypo- della] antiperversa Desh. [a Brachypodella], subula Desh. [type of the later group Mychostoma Alb.], perplicata Fér. [a Brachypo- della], chemnitziana Desh. [type species of the earlier group Apoma Beck], elegans Pfr. [type of the later group Gongylostoma Alb.], crispula Pfr. [a species of the later group Gongylostoma], ? torticol- lis (Oliv.) Lam. [= Clausilia of the section Bitorquata Bttg.]. Another Cylindrella, in Conide, was proposed in 1840 by Swain- son (Malacology, p. 311), and still again, for the group now gener- ally known as Cylichna (t.c. p. 326. See Man. of Conch., XV, p. 287). It is now, so faras we know, impossible to decide whether Pfeiffer’s group was published prior to Swainson’s or vice versa. Cossmann has proposed to substitute the term Disteectria (q. v.) for Cylindrella Pfr. As Cylindrella is later than both Urocoptis and Brachypodella, and the same name was used in the same year for two other groups, we reject it from the nomenclature of this family. 1840. StpHonostoMA Swainson, Treatise on Malacol., pp. 168, 333. For costata Gldg. and fasciata (Encycl. Meth., pl. 461, f. 17). Name preoccupied by Voigt in Vermes, 1836 ; also used in Rotifera, 1832. 1847. Bracnypopisca Agassiz, Nomentlator Zool., Index Uni- versalis, p. 51. An emendation, upon etymological grounds, of Brachypodella Beck. 1850. THaumasta Albers, Die Heliceen, p. 207. Proposed for decollata Nyst, liebmanni Pfr., gruneri Dkr., eylindrus Chemn., san- guinea Pfr., brevis Pfr., binneyana Pfr. The two first species belong to Lucalotlium, the rest to the Jamai- can and Haytien group of large Cylindrellas. Name preoccupied by Perty in Arachnida, 1830. Spartina (q.v.) has been proposed as a substitute, but it is superfluous, as the group is a synonym of Uro- coptis Beck, 1837. 1850. Mycuostoma Albers, Die Heliceen, p. 207. Prsposaee for subula Fér., collaris Fér., gracilicollis Pfr., hanleyana Pfr., pallida Guild., seminuda Adams. In the second edition of Die Heliceen, 1860, p. 37, von Martens selects C. subula as type. — | 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 269 1850. GoncyLosroma Albers, Die Hel., p. 208. Proposed for sowerbyana Pfr., humboldtiana Pfr., rosea Pfr., variegata Pfr., ele- gans Pfr., crispula Pfr., sagraiana Pfr., porrecta Gould, philippiana Pfr. From this list of species, von Martens selected elegans as the type, in Die Heliceen, 1860, p. 38. 1850. Casra Albers, Die Heliceen, p. 208, proposed for elongata Ch. and gracilis Wood, the former selected as type by von Martens, 1860. This group is absolutely equivalent to Apoma Beck, 1837. 1852. SrropHina Morch., Catal. Yoldi, p. 35. Proposed for laterradii Grat. only. 1853. TracHe tia Pfr., Monogr. Hel. Viv., III, p. 564. Proposed for marmorata Shutt., volubilis Morel., porrecta Gld., gracillima Poey, spelunce Pfr., subtilis Morel., gouldiana Pfr., rugeli, Shutt., riisei Pfr., cinerea Pfr., morini Morel., philippiana Pfr., sealarina Shutt. These are mainly slender Brachypodella species. Name preoc- cupied by Scopoli in Aves, 1777, by Serv. in Coleoptera, 1834, and by Westwood in Coleoptera, 1839. It is, therefore, rejected from molluscan nomenclature. 1870. CaLLtonta Crosse & Fischer, Journal de Conch., 1870, p. 18. Based upon one species, Cyl. elliotti Poey. 1880. Eprropra Strebel & Pfeiffer, Beitr. zur Kenntniss der Fauna Mex. Land- und Siisswasser-Conch., Theil IV, pp. 77, 85. Proposed for Cylindrella berendti, polygyra, morini (not of Morelet), apiostoma. This is a valid genus, well distinguished by the dentition and hollow axis. 1891. DisracrrrA Cossmann in Harris and Burrows, Eoc. and Oligoc. Beds Paris Basin, pp. 100, 114. Proposed as a substitute for Cylindrella Pfr. no reason being given for the change. By reference to the list of species originally assigned to Cylindrella, it will be seen that long before the year 1891, every one was amply provided with generic names, Gongylostoma Alb. and Brachypodella Beck including all of them. The name Distectria, therefore, falls asasynonym. Being of even date with Spartina Harr. & Burr. (q.v.), it might possibly dispute supremacy with that term as a generic name for “COylindrella” parisiensis Desh. ; but it is obvious that that species (which, in our opinion, is not a Cylindrella nor a member of the same family), does not require both a generic and subgeneric name. 270 PROCEEDINGS OF THE ACADEMY OF [1898. 189L. Spartina Harris & Burrows, The Eocene and Oligocene Beds of the Paris Basin, pp. 100, 113 (Sept. 28, 1891). Proposed as a substitute for Thawmasia Alb., 1850 (not Perty, 1830-1834). As Thaumasia is based partly on species of Eucalodium (Crosse & Fischer, 1868), and partly on species of Urocoptis (Beck, 18387), the name Spartina falls as a synonym under these groups, unless, indeed, it be retained for the Paris Basin Eocene species described by Deshayes as “Cylindrella” parisiensis, which is the only species mentioned under Spartina by Harris and Burrows. See under Dis- tectria. II. ANALYTICAL KEY TO CYLINDRELLOID GENERA AND THEIR SUBDIVISIONS. (Exclusive of the generally recognized genera Lia, Macroceramus, Eucalo- dium, ete. ). I. Axis of the shell a solid, not perforated, column; teeth of the radula very peculiar, the centrals very narrow, laterals with gouge-shaped cusps. a. Radula with large posterior cusps (ectocones) upon all of the side teeth, which are of similar form, gradually becom- ing smaller from the inner to the outer edge of radula, generally with no abrupt break in size between lateral and marginal teeth; rows slanting, “ en chevron” (Pl. XVII, fig. 5). Genus UROCOPTIS Beck. b. Axis slender and simple, without spiral laminz or other processes. Subgenus Urocoptis. c. Shell large, stout and fusiform ; axis straight. Section Urocoptis s.s. ce’, Shell small, thin and fusiform ; axis straight. Section Cochlodinella P. & V. ce’. Shell small, pillar-shaped ; axis sigmoid below. Section Spirostemma P. & V. _6'. Axis with a single, strong, smooth spiral lamina, median in each whorl. Subgenus ARANGrA P. & V. b’. Axis with two series of hooks curving toward each other, or with a series of oblique nodes or ribs. Subgenus Iprosremma P. & V. b°. Axis with a single stout spiral fold crenulated at the edge, Section Maceo P. & V. b'. Axis with one or several spiral laminz, the lower of 1898.] NATURAL SCIENCES OF PHILADELPHIA. 271 which is cut into teeth or crenulated, at least in the earlier whorls. Subgenus GonGyLosroma Alb. Cc. Three to seven spiral laminze developed, increas- ing in size from the upper to the lowest one, which is largest. Section Pycnoptychia P. & V. . Three laminz, the lowest smallest, upper largest. Section Callonia C. & F. . Two subequal spirals; a median whorl with ’ accessory laminz upon the upper and _ basal walls. Section Sectilumen P. & V. . Two spirals, the lower dentate in upper whorls, and in an intermediate whorl expanding into a very broad, flat or cup-like plate. Section Esochara P. & V. . Two gradually increasing spirals, the lower cren- ulate or denticulate; sometimes a short, low, third spiral interposed in an intermediate whorl. Section Gongylostoma s. str. . Two strong, subequal spirals, both crenulated or denticulate (Haiti). Section Amphicosmia P. & V. . One incised or denticulate lower lamina with sometimes a smaller one above it. Section Tomelasmus P. & V. a’. Radula with the posterior cusp (ectocone) sub-obsolete or wanting on the first or both lateral teeth ; two laterals on each side enormously developed, the marginals abruptly smaller, narrow, probably functionless, with vestigial cusps ; arranged in horizontal lines (Pl. XVII fig. 4). Axis of the shell without lamine. Genus BRACHYPODELLA Beck. b. Inner lateral tooth with a vestigial posterior cusp (ecto- cone) without cutting point; outer lateral with cut- ting point developed on the ectocone. c. c. Subgenus BRACHYPODELLA. Axis slender throughout, rarely with a small spiral fold ; shell slender and elongate. Section Brachypodella s, str. Axis strong, heavily calloused ; shell obese. Section Strophina Mérch. 272 PROCEEDINGS OF THE ACADEMY OF [1898. b'. Inner lateral tooth with no ectocone; that of the outer lateral without cutting point. Species all Ja- maican, c. Axis slender, straight; last whorl of shell be- coming free, and keeled below; aperture subcir- cular, angular below, as wide as high. d. Shell small, narrowly fusiform, with strong- ly ribbed whorls. Section Geoscala P. & V. d', Shell slender, pillar-like, white and smooth, of many narrow whorls. Section Mychostoma Alb. c'. Axis a mere edge of contact between whorls ; shell white, sinistral, slender, of many oblique whorls, the last not free; aperture oval, longer than wide. Section Apoma Beck. II. Axis of the shell a hollow column; radula of normal form and arrangement; central teeth tricuspid, short and wide; laterals numerous, similar, bicuspid ; marginals wide, very short, multi- cuspid (Pl. XVII, fig. 2). a. Shell very slender and elongate, thin, not conspicuously calcareous, the axis subcylindrical or bulging in each whorl, usually rugose. Genus EPIROBIA S. & P. a‘, Shell stout, pupiform, with entire spire, conspicuously cal- careous, ete., ete. Genus HOLOSPIRA Mart. III. CLASSIFIED LISTS OF SPECIES. As the groups defined by us in the preceding table of classification differ radically in limits from those hitherto accepted, it is necessary to supplement the characterization of the genera and subgenera by detailed lists of species. These lists contain only species whose characters we have ascertained by the examination of sections. Those we have not been able to examine are omitted,’ although a large part of them could doubtless be approximately grouped by the published information. The names of species of which the radula is known are distin- guished by the following symbols: “(CF)” after the name of a species indicates that the dentition has been examined by Crosse & ‘ The lists are, therefore, a catalogue of the species in the collection of the Academy, excluding a considerable number of doubtful, unidentified or new species. Any forms not mentioned herein we will be glad to receive and offer an exchange for. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 273 Fischer ;> “‘(B.)” that it has been examined by W. G. Binney ; “(S P.)” by Strebel & Pfeffer ;’ “(P V.)” by ourselves. Genus UROCOPTIS Beck. This genus is restricted to Cuba, Jamaica and Haiti, with a few stragglers from the Cuban fauna in south Florida. It is practi- cally a group of the Greater Antilles. The typical forms, with the axis simple, are the most widely spread and probably the oldest type. The large, stout forms being a local development common to Jamaica and Haiti. The forms with spiral folds or other ornamentation of the axis are confined to Cuba and the adjacent portion of Haiti. There is every reason to believe them autochthonous to Cuban soil, a few species recently spreading eastward. This genus shows the bond between Jamaica and Haiti to be rather stronger than between Cuba and Haiti, the Cuban groups occurring in Haiti being represented by very few species, and these restricted to the extreme western end of the island. The elements common to Jamaica and Cuba are the more general- ized and presumably older sectional groups of the genus. Respecting the habits and environment of the Jamaican Cylin- drellas of both the genera Urocoptis and Brachypodella, Mr. Charles T. Simpson writes of the experiences of Mr. J. B. Henderson and himself, as follows: “CO. sanguinea, rosea, obesa, cylindrus, aspera, brevis and allied forms live on the ground among the serub and dead leaves, and are of just about the color of their surroundings. We found C. nobilior abundant in a talus of decomposed shaly rock at Bogwalk, of which it was almost exactly the color. C. seminuda, alba and robertsi are found in the crevices of craggy limestone rocks, among cliffs. C. rubra and tenella live in the ground in thickets where there is abundance of dead and decaying wood. The shells, in form and color, always look exactly like pieces of broken twigs, which are found abundantly with them, and it was a long time before Henderson and I found a single specimen, They are very abundant though in proper localities. C. gracilis Wood grows invariably on the trunks and stems of trees in thick scrub. These trees have grayish or whitish spotted bark; the little rascals attach themselves to it by the foot and stand out with the shell nearly at 5 Journal de Conchyliologie, 1870. ® Ann. N. Y. Acad. Sci., IL. 7 Beitr. Mex. Moll. 274 PROCEEDINGS OF THE ACADEMY OF [1898. right angles to the trunk or limb, and as the shell is always more or less dirty, the resemblance to a thorn is so astonishing that we doubtless passed by thousands of them, never dreaming for a mo- ment that they were Cylindrellas.” Mr. Uselma C. Smith found B. elongata living on limestone cliffs, upon which the white shells hung like stalactites, for which he at first mistook them. Subgenus Urocoptis Beck. Type U. eylindrus (Chemn.), P}]. XVIII, fig. 11 (axis) and Pl. XVII, fig. 5 (dentition). Section Urocoptis, s. s. Species of Jamaica. U. amethystina (Chitty). U. megacheila (Chitty). U. aspera (Ad.). U. nobilior (Ad.). U. baquieana (Chitty). U. procera (Ad.). U. brevis (Pfr.) [C F.]. | U. rosea (C. B. Ad. not Pfr.) U. carnea (Ad.). | (CF Bs, Pos eae U. eylindrus (Chemn.). U. sanguinea (Pfr.) [C F.]. U. gravesii (Ad.). U. zonata (Ad.). U. lata (Ad.). Species of Hayti. U. adamsiana (Pfr.). U. gruneri (Pfr.). U. areuata (W. & M.). U. guigouana (Petit). U. crenata (W. & M.). U. mabuja (Weinl.). U. eugenii (Dohrn). U. malleata (Pfr.). U. eximia (Pfr.). U. menkeana (Pfr.). U. flammulata (Pfr.). U. puncturata (Pfr.). Section CocHLODINELLA Pils. & Van. Type U. poeyana (Orb.). Radula with 12.1.12 teeth, which are typical for the genus in form, but decrease rather rapjdly. Species of Cuba and Florida. U. angulifera (Gundl.). U. mamillata (Wright). U. atropurpurea (Arango). U. mixta (Wright). U. goniostoma (Gundl.). U. paradoxa (Arango). U. illamellata (Wright). U. poeyana (Orb.) [B., P V.J. U. jejuna (Gld.). U. presasiana (Pfr.). U. lactaria (Gld.). U. variegata (Pfr.). 1898.} NATURAL SCIENCES OF PHILADELPHIA. 275 Species of Jamaica. U. auguste (C. B. Ad.). U. pupeformis (C. B. Ad.). U. hollandi (C. B. Ad.). | U. striata (Chitty). U. hydrophana (Chitty). | Section SprrosTemMA Pils. & Van. Type U. rubra (C. B. Ad.), Pl. XVIII, fig. 12. The species are all Jamaican. U. dunkeriana (Pfr.). U. rubra (C. B. Ad.). U. montana (C. B. Ad.). | U. similis (C. B. Ad.). U. princeps (C. B. Ad.). U. tenella (C. B. Ad.). U. pusilla (C. B. Ad.). | U. tenera (C.B. Ad.). Subgenus Arangia Pils. & Van. Type C. sowerbiana Pfr., Pl. XVIII, fig. 20. Subgeneric name in memory of the Cuban naturalist, Rafeal Arango. U. sowerbiana Pfr., Cuba. | U. monticola Wein]. Gonave I. Subgenus Idiostemma Pils. & Van. Type C. uncata Gundl., Pl. XVII, fig. 10. A Cuban group, containing some of the most peculiar species of the genus. There is a series of species leading by gradual stages from the axial pairs of hooks of the typical forms to the oblique nodes or ribs of U. lateralis, ete. U. uneata (Gundl.). U. geminata (Pfr.). U. perlata (Gundl.) (C F., P.V.] | U. fastigata (Gundl.). U. levigata (Gundl.). U. lineata (Gundl.). U. intusmalleata (Gundl.). | U. lateralis (Paz.) [P V.]. Section Macro Pils. & Van. Radula with the teeth very rapidly decreasing, the third decidedly smaller than second, formula about 8.1.8. Subgeneric name in honor of a Cuban patriot. U. interrupta (Gundl.) [P V.], Cuba. Pl. XVII, fig. 7. Subgenus Gongylostoma Albers. Section Pycnoptycuia Pils. & Van. Type U. humboldtiana (Pfr.), Pl. XVIII, fig. 14. Species all Cuban. : U. humboldtiana (Pfr.) [B.]. U. striatella (Wright). U. oviediana (D. Orb.). U. trilamellata (Pfr.). U. sceeva (Gundl.) [C F.}. _| U. vignalensis (Wright) [C F). U. shuttleworthiana (Poey). 276 PROCEEDINGS OF THE ACADEMY OF [1898. Section CALLONIA Crosse & Fischer. Type C. elliottii Poey. Radula typical. See Pl. X VIII, fig. 18, U. dautzenbergiana (Crosse). Species all Cuban. We have enlarged the group of Crosse and Fischer to include other Cuban species having the same internal structure and denti- tion. Species elaborately sculptured with hollow ribs :— U. elliottii (Poey) [C F.]. U. dautzenbergiana (Crosse) Pav Somewhat smooth species :— U. brunnescens (Gundl.). U. notata (Gundl.). U. clara (Wright). U. vineta (Gundl.). U. guirensis (Gundl.). U. saxosa (Poey). U. infortunata (Arango). Species with beaded suture :— U. albocrenata (Gundl.) Section SECTILUMEN Pils. & Van. U. ornata (Gundl.) [B., P V.]. Cuba. Pl. XVII, fig. 9. Section EsocHara Pils. & Van. Type U. strangulata (Poey), Pl. XVIII, fig. 15. Distribution, Cuba. U. fabreana (Poey) [P V.]. | U. teneriensis (Wright). U. strangulata (Poey). | Section GONGYLOSTOMA Albers (restricted ). Type U. elegans (Pfr.), Pl. XVIII, fig. 17 (variety). Also Pl. XVIIL, fig. 16, U. pruinosa. Distribution, Cuba. U. artemesie (Gundl.). U. fortis (Gundl.). U. auberiana (D. Orb.). U. gutierezi (Arango). U. conereta (Gundl.). U. lavalleana (Orb.). U. coronadoi (Arang). U. obliqua (Pfr.). U. crispula (Pfr.). U. planospira (Pfr.). U. elegans (Pfr.) [B., P V.]. | U. pruinosa (Morel.) [P V.]. Section ToMELAsMus Pils. & Van. Type U. torquata (Morel.), Pl. XVII, fig. 8; also Pl. XVIII, fig. 13, U. wrighti var. Radula typical. Species all Cuban. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 277 U. aculeus (Morel.). U. heynemani (Pfr.). U. acus (Pfr.). U. hidalgoi (Arango). U. adnata (Pfr.). U. hilleri (Pfr.) [P V.]. U. afinis (Pfr.) [P V.]. | U. incerta (Arango). U. angustior (Wright). U. integra (Pfr.). U. arcustriata (Wr.). U. irrorata (Gundl.). U. assimilis (Arango). U. macra (Wright). U. eapillacea (Pfr.). U. plumbea (Wright). U. coerulans (Poey). U. producta (Gundl.). U. colorata (Arango). | U. sawvalleana (Gundl.) [P V.]. U. crenulata (Gdl.). | U. seabrosa (Gundl.). U. erystallina (Wright). U. thomsoni (Arango). U. decolorata (Gundl.). | U. torquata (Morel.). U. diaphana (Wright). _ *U. unguiculata (Arango). U. discors (Poey). U. ventricosa (Gundl.) [P V.] U. fibrosa (Gundl.). | U. violacea (Wright). U. fusiformis (Wr.). U. wrighti (Pfr.). U. gareiana (Wright). Section AMPHICOSMIA Pils. & Van. Type C. salleana Pfr., Pl. XVIII, fig. 22. Proposed for three San Domingo species in which the columella bears two spiral laminz, both finely denticulate. U. salleana (Pfr.). U. gracilicollis (Auct.). U. hjalmarsoni (Pfr.). Genus BRACHYPODELLA Beck, 1838. In this genus the radula is more highly specialized than in Uro- coptis and the shell generally less so, internal armature of the axis being entirely absent, or limited to a weak, scarcely noticeable, spiral fold above. The geographic range of Brachypodella includes not only the ter- ritory occupied by Urocoptis, but surpasses it on all sides: in the Bahamas on the north, the Virgin group on the east, the whole Caribbean chain and northern border of South America on the south, and west and southwest is sparsely distributed over Central America and southeastern Mexico. The distribution of the minor groups is suggestive. The Jamai- ean sections form a group by themselves characterized by the ex- tremely aberrant dentition as well as the modified shells. The spe- cies of other islands and the mainland are decidedly less specialized, 278 PROCEEDINGS OF THE ACADEMY OF [1898. and show but a small amount of variation in general appearance. The section Strophina has the dentition of typical Brachypodella. Section BRACHYPODELLA s. 8. Type B. antiperversa Fér. This subgenus has a less specialized radula and wider geographic range than the others. The species are all small, mainly quite slen- der forms, for the most part not exhibiting great variety of form ; but two exceptions may be noticed: B. brooksiana of Cuba, and some related species, have the neck enormously drawn out; while in some of the continental forms there is a weak spiral lamina upon the pillar. Continental Species: Tabasco and Yucatan to Venezuela. B. bourguignatiana (Ancey). B. spelunce (Morel.). B. hanleyana (Pfr.). B. spelunce var. dubia (Pils.). B. morini (Morel.). B. subtilis (Morel.). Insular species: Curacao and Trinidad to Porto Rico. B. raveni (Bld.). Curacao. BL. pallida (Gldg.). St. John, B. trinitaria oe )[P V.]. Trin- Tortola, St. Thomas, Porto idad. Rico. B. costata (Gldg.) [C F.]. Bar- | B. chordata (Pfr.). St. Croix. bados. B. portoricensis (Pfr.). Porto B. antiperversa (Fér.) [P V.]. Rico. . | Guadeloupe. B. riisei (Pfr.) [P V.]. Porto B. collaris (Auct.) [P V.]. Gua- Rico. deloupe, Martinique. Greater Antilles— Haiti. B. dominicensis (Pfr.). B. smithiana (Pfr.). B. gouldiana (Pfr.). B. weinlandi (Pfr.). B. obesa (Weinl. & Mts.). Greater Antilles— Cuba. B. blainiana (Gundl.). B. modesta (Poey). B. brooksiana (Gdl.) [C F., P. | B. philippiana (Pfr.). WJ: B. plicata (Poey) [P V.]. B. camoensis (Pfr.). B. porrecta (Gld.). B. capillacea (Pfr.). | B. rugeli (Shutt.). B. cyclostoma (Pfr.) [B., P V.]. | B. sealarina (Shutt.). 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 279 B. gracillima (Poey). | B. seopulosa (Gundl.). B. gundlachiana (Poey). B. sexdecimalis (Jien.). B. marmorata (Shutt. ). | B. soluta (Pfr.). B. minuta (Gundl.). |B. turcasiana (Gundl.). Bahamas. B. bahamensis (Pfr.). New Providence, [C F., P V.]. Section SrroPpHINA Morch. B. laterradii (Grat.) [P V.]. San Domingo. Section Groscata Pils. & Van. Type B. seminuda (C. B. Ads.). A Jamaican group similar to some Brachypodellas except in the dentition, which is of the highly evolved type seen in Mychostoma. The shell differs from this last group in being fusiform, fewer whorled and strongly costate. B. seminuda (C. B. Ad.) [B., P | B. inornata (C. B. Ad.). V.j. | B. robertsi (C. B. Ad.). B. costulata (C. B. Ad.). | Subgenus Mychostoma Albers. Mychostoma Alb., Die Hel. (edit. 1), p. 207. All species are Jamaican. B. agnesiana (C. B. Ad.) [C F., | B. alabastrina (Pfr.). i Val _ B. pearmaniana (Chitty). B. alba (Ad.). B. subula (Fér.) [B.]. Subgenus Apoma Beck. Apoma Beck, Index Moll., p. 89. Casta Alb., Die Hel., p. 208. A very distinct group, containing two sinistral Jamaican species. Type Turbo elongatus (Wood), Pl. XVIII, fig. 21. Von Martens objects to the name Apoma because of its inapplica- bility as implying that other allied groups should be operculated ; but it was obviously given to direct attention to the most conspicu- ous difference between this group and Clausilia, and from this point of view is eminently appropriate. B. gracilis (Wood) [C F., 8 P.]. | B. elongata (Chemn.) [B., P V.]. g g Genus ANOMA Albers. 1850. Anoma Alb., Die Heliceen, p. 209, for acus Pfr., gossei Pfr., tricolor Pfr. (the last selected as type by von Martens, Die Hel. 2d edit., 1860, p. 269). Not Anomus Fairm. Hemiptera 1846. 280 PROCEEDINGS OF THE ACADEMY OF [1898. 1850. Leia Albers, Die Hel., p. 207. Sole species LZ. maugert Wood. Not Leia Meigen in Diptera, 1818, nor Meg., Coleoptera, 1821. 1852. Lia Moreh, Catal. Yoldi, p. 35. Sole species LD. maugeri. Not Lia Esch., in Coleoptera, 1829. 1869. Inliaculus Schaufuss, in Paetel’s Moll. Syst. et Catal., p. 15. 1894. Vendrysia Simpson, Proc. U. 8. Nat. Mus., xvii, p. 480. Substitute for Leia. Distribution, Jamaica; mountains of the interior. Of the several names proposed for this group, Anoma has priority. It has the disadvantage of being preceded by Anomus, which some writers would hold to be identical. Those adhering to this view will adopt the name Jnliaculus of Schaufuss ; but pending some con- certed action upon this point in “nymology” the oldest name may be allowed to stand. The dentition (Pl. XVII, figs. 8 and 6, A. maugeri) is extremely peculiar, differing from that of Urocoptis in having the cusps of the teeth serrate. A. maugert (Wood). A, zebrina (Pfr.). A. blandiana (Pfr.). A. tricolor (Pfr.). A. macrostoma (Pfr.). A. gossei (Pfr.). Genus MACROCERAMUS Guilding. 1822. Cochlodina, Lre groupe, Pupoides Fér., Tabl. Systematique, p. 24, 61. 1828. Macroceramus Guilding, Zool. Journ., IV, p. 168. M. signatus. 1850. Colobus Alb., Die Heliceen p.177. Not of Illiger, 1811, Merrian, 1820 (Rept.), or Serv., 1833 (Coleopt.). For anatomy see Crosse & Fischer, Journ. de Conchyl., 1870, p. 20; Moll. Terr. Mex., I, p.419. Binney, Terr. Moll., V, p. 384; Ann. N. Y. Acad., III, p. 126. Strebel & Pfeffer, Beitr. Mex. L. u. S.-W. Conch., IV, p. 89. Preponderantly Antillean, this genus has representatives upon the mainland bordering the Gulf of Mexico from Venezuela to Florida. These peripheral species are apparently all members of the section Microceramus. In the West Indies the genus is present on nearly every island, but is especially developed in Cuba, to which Spiro- ceramus is confined. It is poorly represented in Jamaica by a few species of the group Microceramus, to which the species of the Bahamas likewise belong. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 281 Synopsis of subgenera. I. Axis slender, straight and simple. a. Macroceramus. Shell comparatively solid and large. Type M. signatus Gldg. a’. Microceramus Pils. & Van., (n. s.-g.). Shell smaller, thin. Type W. floridanus Pils. Il. Axis with a strong spiral lamina. Spiroceramus Pils. & Van., (n. s.-g.). Dentition unknown. Type M. amplus Gundl. Genus PINERIA Poey. This small group, originally described from the Isle of Pines, but also occurring in several of the Caribbean Islands, is probably an offshoot of the genus Macroceramus. The peculiar features of the external anatomy described by Poey should be re-examined. Genus EPIROBIA Strebel & Pfeffer, 1880. Epirobia 8. & P., Beitrag zur Kenntniss der Fauna mexikanischer Land- u. Siisswasser-Conchylien, Theil LV, pp. 77, 85. Type E. polygyra Pfr. Pl. XVII, fig. 2 (dentition). For figure of the axis, see Strebel, /. c., pl. 14, f. 14. Many-whorled, slender species of Eastern Mexico, usually retain- ing the spire intact, differing from Urocoptis and Brachypodella in dentition and in the hollow axis. Notwithstanding the entirely “ Cylindrella”’-like aspect of the shell externally, these features un- questionably locate the group near Holospira and Celocentrum. Strebel and Pfeffer referred all of the Mexican Cylindrellas to their group; but it must be restricted by removal of the forms with solid axis, which apparently belong to Brachypodella. In addition to the two species mentioned below, FE. berendti Pfr. [S P.] belongs here, and probably gassiesi Pfr. and swiftiana Crosse also. The * E. morini Morelet,” of Strebel & Pfeffer was incorrectly identified,and probably a form of E. polygyra.’ The true C. morini is a Brachy- podella with acutely keeled base. E. polygyra Pfr. [S P., P V.]. E. apiostoma Pfr. SSince this paper was written, this form has been referred by Dr. yon Martens to C. folygyrel/a Mts. It is a true Z/irodia. 19 282 PROCEEDINGS OF THE ACADEMY OF [1898. Genus HOLOSPIRA von Martens. This genus, which is confined to the mainland of Mexico and the adjacent States of the Union, offers an interesting series of structures in the internal lamelle, parallel to those of Urocoptis. The prin- cipal divergence from that genus is in the frequent development of parietal and basal lamellz, which are of rare occurrence in the Antillean genera. Professor Dall,? who has ably investigated the subject, gives the following classification, which seems worthy of unqualified ap- proval :— Subgenus Hotosprra s. s., type WN. pilocerei Pfr., with section Bostrichocentrum Strebel & Pfeffer, Haplostemma, Eudistemma and Distomospira Dall. Subgenus Merasroma Strebel & Pfeffer, type H. roemeri Pfr. Subgenus CazLosteMMA Dall, type H. elizabethe Pilsbry. The first group includes species with an axial plait and usually various other armature. More or less similar structures occur in Gongylostoma. Metastoma has the axis simple, as in typical Urocop- tis and Brachypodella. In Celostemma a swollen, vertically cost- ulate axis is found, unlike any Antillean type, although there is some analogy with the subgenus Jdiostemma Pils. & Van. Genus EUCALODIUM Crosse & Fischer. In this Mexican genus the large, solid shell resembles typical Uro- coptis; the axis is solid and sinuous, with a continuous spiral plait, as in the subgenus Arangia P. & V., of Urocoptis. The subgenus Oligostylus Pils.” has the axis straight and smooth, as in typical Urocoptis. These two types of pillar are exactly paralleled also in the genus Macroceramus Gldg. and its subgenus Spiroceramus Pils. & Van. Subgenus Anisospira Strebel & Pfeffer. An eastern Mexican group, of few species. The soft anatomy is still unknown. It seems to be a subgenus subordinate to Hucalo- dium. Genus BERENDTIA Crosse & Fischer. Like Spurtocentrum, to which it is closely allied ; but with the axis solid, slender and smooth, and the spire tapering, with fewer, more % Proc. U. S. National Museum, xix, p. 344, 1896. 19See Dall, The Nautilus 1X, p. 51; Proc. U. 8. Nat. Mus. XIX, p. 348. 1898.] NATURAL SCIENCES OF PHILADELPHIA. 283 rapidly widening whorls. ‘The only species, B. taylori Pfr., inhabits the table land of Lower California. Genus CHLOCENTRUM Crosse & Fischer. The hollow and usually vertically ribbed axis is unlike any of the Antillean types, although radiating spines, such as Dall describes in C. astrophorea, recall certain forms of Gongylostoma. In the section Spartocentrum Dall” there is a spiral inflation and no vertical rib- lets. . Genus CERION (Bolt.) Mérch. See Proc. Acad. Nat. Sci. Phila., 1896, p. 315. This genus has generally been placed in the neighborhood of Pupa, but it is not closely allied to that group in shell characters and is entirely diverse in genitalia. It may possibly belong to the Odontostomine ( Odontostomus, Tomigerus, Anastoma) of South A mer- ica; but we prefer to associate Cerion with the Holospira and Euca- lodium groups of Urocoptide.” As this genus has been made the subject of special papers by Dr. W. H. Dall and by the present writers, it need only be said here that it differs from the other genera in being strictly littoral in dis- tribution, never straying far from the seashore. The Miocene forms ( Eostrophia) are probably aberrant rather than primitive, in lack- ing parietal and axial lamine. Genus MEGASPIRA Lea. A Brazilian group very peculiar in its polygyrate shell with large, rounded nuclear whorls, plicate columella and peculiar internal arma- ture, somewhat recalling Gongylostoma, Idiostemma, etc. This has been described and figured by Gabb.” The dentition we have now examined (Pl. XVII, fig. 1), the radula having been found in a dry shell. There are 28°1°28 teeth, arranged in slightly sinuous trans- verse rows, and of the type usual in ground snails, much like those of Eucalodium, Berendtia, ete. ™ See Nautilus IX, p. 51 (Sept., 1895), type Calocentrum irregulare Gabb. The genus Teneritia Mabille, Bull. Soc. Philomathique de Paris, (Ser. 8), Vol. IX, p. 79( 1897 or 1898) isa synonym of Spartocentrum. Types Berendtia digueti and B. minorina Mabille. M. Mabille is perfectly right in separating his group from Berendtia, but he overlooks the only really important differential character, viz., the hollow axis. 1? Dall has hinted at the same relationship. See Proc. U. 8. Nat. Mus., XIX, p. 347, 348, 1897. 1° American Journal of Conchology LI, p. 64. 284 PROCEEDINGS OF THE ACADEMY OF [1898. Megaspira was placed in the vicinity of Clausilia by Deshayes, who thought the internal structure indicated the presence of a clausi- lium. This inference does not seem justified by the facts of the case, though we are far from denying its possibility; our specimen with the soft parts dried in shows no trace of a clausilium. Upon the whole, it would appear that Megaspira is an aberrant member of the Urocoptide, nearest perhaps to Eucalodium among existing genera. The South African genus Celazis and the Papuan and Australian Perrieria are somewhat similar to the foregoing American genera, but are doubtless correctly referred to Pupida, near Clausilia. Per- rieria has a complicated internal armature, only partially worked out by Fischer. The Colombian Rhodea is probably referable to the Achatinide, grouping near Subulina Beck (type S. octona). TABLE SHOWING GEOGRAPHIC DISTRIBUTION OF THE UROCOPTIDA. Genus UROCOPRTIAN. <.c.cecccsccsscsesrnn Section Urocoftis (restricted)... Section Cochlodinella......ccccs0e Section SPirostemmMa.....ce creer Subgenus Arangia.....0. v0 Subgenus /diostesti1....ccccseeveee Section Maceo. ......c.cssc00 Subgenus Gongylostoma..... eas Section Pycnoptychia...ecee.e+++ Section Calonia............ccesessee Section Sectz/umen ... Section Lsochara. ..sccccscsscersese Section Gongylostoma (Ss. 5.).+.+ Section AmPAiCOSMIG .0000 veceeeees Section Torelasmus....c.cccccesses Genus BRACHYPODELLA ........000000 Section Brachypodella (s.5.)... Section StropAind.......cssccccseeee Section Goscala.ccece..-scoscecerses Section Mychostoma......cseo Section Afoma Genus EPIROBIA F Genus HOLOSPEEAS. «0. < Geo. Farnum and J. Epw. Farnum. Human Cranium, Mon- golia. q Miss J. A. Fuaniaan. Indian Tanned deer skin, Western, N. A. Esrate or Geo. H. Horn. Various specimens, Arrow points, ete. Epw. Lonesrreru. Several miscellaneous specimens. ; CLARENCE B. Moore. Various important additions to the Moore collection of mound implements, ete. PLANTS. SrewARDsON Brown. Four hundred species, Pennsylvania plants; two hundred and fifty species plants from the Northwest coast; one hundred and fifty species plants herbarium of Wm. Boo JoserH Crawrorp. ‘Two hundred and fifty species of No rh American plants. si Anna C. Hortsnorne. Six hundred and seventy species of Japan ese plants. Tsomas Meewan. Eight hundred species of South African plants. ‘ C. F.Saunpers. Two hundred and fifty species of Pennsylvania — plants. J. W. Eckretpt, M.D. The entire Eckfeldt Collection of Lichens. 1898. ] NATURAL SCIENCES OF PHILADELPHIA. 531 INDEX TO GENERA, ETC., 1898. By en A ee 378 | Ammospermophilus . . . 123 i oe Rly sk hice 419 | Amorpha ere eaten 21, 297 ONG. ees | RMA cn et cae 84 Acalypha 389 Amphichena . ee Acanthacee . 391 | Amphicosmia . 271, 277 Acanthochitide. . .. . 288 | Amphiprora ....« «. 112 mecpitey....... 80, 209 | Amphisbeena . 103-105 Cas 5i ve. ca: 21, 297 | Amphisbenide . 103 a 190 | Amphispiza 214 NO ss 30, 304 | Ampullaria. ...... 106 Acroceride....... 161 | Anacardiaceze 381 See Get | RRB) By fw a 419 Actinocyclus . . . 423) Anadenulus 220, 222, 229, 254 Actinoptychus 423, 424 Anadenus ....... 220 meee TG, 200 | ARORRINS oo oh ck ee 381 Adiantum . 409 | Anaphalantus 162 Egialitis. . . . 207 | Anastoma 283 Se ee (2 | Anatidye . . 606s ee 137 Aschninw ..... PS OTS er eee , 148 Ae 395, 412 | Anemone . 16, 17, 293 Agelaius. .... 82, 212 | Angelica . . 302, 405 Agrionine . 142, 147 Anguidse 4 1a Agropyron. . 45, 314 | Anisolepis . ... . 102, 104 [ae 45, 313 | Anisospira . Ls See atts kc a a “wate 78 | Anoma . . 279 Alactaga. .... . . 121 | Anomia . 462 Alaria . . . 462) Anona . . 410 Alcide 127, 495 | Anonacer . 410 ee Ee 383 Anthericum 397 Allionia . . . 89 | Anthomyia 162 0 SS ee 42, 312 | Anthomyide . 162 See a Qk | Anthraxm. . «6 3): 158 Anochura...... 462, 463 | Antirrhinum...... 38 Amaryllidacew ..... 895 | Antrostomus .... . 81 ee ae 103 | Aphallarion 219, 222, 228, Amelanchior . . . . 24, 299 | 226, 228, 235 UO. Sw pie 30 | Aphelocooma ...... 212 Ammodramus 83, 139 Aplopappus. . . . 30,31, 304 532 PROCEEDINGS OF THE ACADEMY OF [1898 MORN Gee gree 193 | Berbers... eee 48 mee he os Ga 445 | Berendtia ..... 282, 283 ReCMS .- 268,272; 279 :| Betwla ysl yo. san 41, 311 SC RC ae 492 Biddulphia. . . 423, 468-470 EUR. Peon ie ond ine say 209 | Bidens ns). «2 ee 385 Ayalinces ~ | 23's)... tas 4 411 Bigelowia. . 32, 33, 305 ei eet fel 498 | Bignoniacee ...... 386 i 270, 275 | Binneya 220, 222, 224, 227, Arbutus . . . . 35, 307 229, 232 ct a ae ae 418, 419, 421 | Binmneyine ....... 227 Brctomya 6) J iscsi 123, 352) Blechnum . . 2. agen 47 miretometta . . .. « «8s 4s 137 | Blenniids . ...-. soe 346 Arctostaphylos . . 30, 306 | Blennius. .-. .-. 37m 346 Mnteg t eC ORRG 78, 207 eA oS Ae eee 105, 106 Arenaria. 0. A 319, 402 | Boide . ... 5 48s 105, 108 AS POMIGNG Ss: (2) 0s, en 4 379 | Bombycide ...... 158 Ariolimacine . . 220, 222, 227 | Bombylius....... 159 Ariolimax 219-222, 224, Bonasa . . . . <7 79 226, 228, 232, 235-237 | Boraginacee ...... 399 Mad fe? se 220-226, 239 | Borus:. . |. . < . 2 ae 106 Arionide ... . .. 220-222 | Boutelona . . . ~ mamas 387 Arionms . oi. loge 226: | Box . 20s, 6 oss Sean 342 Artemisia . 31, 32, 304, 305 | Brachyphylla..... . 333 POEUN a os ae 358 | Brachypodella . 267, 269, IIE 5 ig haut oe are, (ot 59-61 271, 277, 281 mesa rine s.r Mais. 159 | Brachypodisca .... . 268 BCHOMIYS . 368-370 | Brachypodium .... . 401 Asclepiadacee . 390,405, 411 | Brachypus....... 267 i CT a ne 90, 405 | Branta ... .. . = 138 ANT | i Se ae 158 | Brebissonia . . . «am 112 Aspiimim . 9. 4°: . 47, 314 | Brodiza . .... 29 42, 312 ae are 32,:305;.378 | Babo’. . | # > (eae 80 Astragalus . . . 21, 297, 404 | Buccinids . . . . Gay 190 POR a ss es Ber 418 | ‘Buddleia. « . :. ge 405 PARED ee ace 340 | Buliminus : .. . 73 265 Peer ae KES $40'| Balimog . .. . > 2am 106 Atriplex. . 39, 310, 375 | Buphthalmum .... . 32 Aulacodiscus ...... AZ) ‘Bates... o.e < veaee 80, 209 penne 3. Ss 423 | Cactacee. . . . 386, 389, £10 Th ee 101,/192'| Cadalus ... ...+ i) ae 419 8 i) ee eee ee es) 140'| Caecum .. < . +305 418 BACWISeIA».. S- ss) 2 BMY 113 | Celocentrum .... «5 281 Balan. os) oa A19 | Cusalpinia. - «...%% 354 Balsamorrhiza 32;:805 |(Caiman. . .. 27 101 arieeng 5 |! ube ie 79 | Calandrinia. . . . = 2% 393 a 38, 49 | Calcatius... . . Ae 139 Dazania. <5. «4 47, 315 | Calligonum. ...... 39 Belogona ...... 67, 68 | Callipepla....... 208 1898.] NATURAL SCIENCES OF PHILADELPHIA. 533 SS See 419 | Chetopleura ...... 288 Callistochiton. ..... 288 | Chetura ...... 81, 211 mmm .. . . 269,271, 276 | Chamea ......°.. 218 Callospermophilus. . . . 123 | Charterginus. . . . 458-460 Calochortus 43, 312, 388 | Chartergus. .. . . 457, 458 Calophanes. ...... 391 | Cheilanthes ...... 387 OS ee 42, 312 | Chelidon® ..... 84, 216 ere 211 |} Ohalydids.... . 2). ; 101 ss 8°. = 2 WAS, GAs | ONO. Gh oa 138 Campylodiscus 429, 423, 425 | Chenopodium. . ... . 375 Camptonectes. ..... 462 | Chilonatalus ...... 326 Seta... . . 87 | Chilonycteris. ..... 326 IS ao, en Lemone” 2. Ae 419 A 124 | Cheronycteris ..... 333 Caprifoliacee. ..... 400 | Chondestes....... 214 Caprifolium ...... 30 | Chordeiles . . 81, 210, 211 SN show ow’ we GO| Darema. es oa ee 343 Sg ws es 223 | Chrysocoma ...... 32 ee Gas | Camynone: 3 uh ae eke fs 157 Cardiospermum .... . Soe | CaRuia. ew. ale ee 462 Mergiam...... 419; 462 | Circinaria’ . . . / ... 244 ee ae See: | SeOld 2° Sede 80, 208 | Se oe Ree } Cleese > ee 21, 297 | CE Per oot teenie” V4 dee ete 137 Carpodacus.... . on, vie | Olarkia . . . £73" % 28, 302 SS eg Se 303 | Clausilia . 265-267, 284 Caryophyllacee 379, 388, Claytonia. . 19, 20, 295, 402 402,410 | Clematis 15, 17, 293, 388 IN 4) "52 os a 393 | Cleome. .... 16,18, 294 IS er Wee |} Chae ae el es 217 SE 400, 407 | Clupanodon ...... 340 OS eee el ee a Pg 340 Ceanothus. . 20, 48, 296, 395 | Cnemiornis. ..... . 496 Cecomorphe ...... 495 | Cincus. . . . . 33, 305, 385 Centrolabrus ...... Sas | Cees (S54, are ees 382 Centrophorus. .... . 889 | Coccyzus ......-. 80 Semtropyxs .... . 103, 104 | Cochlodina. . . 266, 267, 280 Ceophleus 81, 210 | Cochlodinella. . . . 270, 274 ee 68 | Colaxis ..... ‘vce a 129 | Celocentrum...... 283 Cerastium . 18, 294, 402 | Celostemma ...... 282 Cerataulus . 423, 425 | Colaptes...... 81, 210 Cercosaura....... ee Re ee oad ee 79 ae ee ae 496 | Colletes....... 51-53 Cereus . 373,889, 410 | Collinsia. ....... 38 Cerion . . 283,475-478 | Collomia. . ... . 36, 308 DLE) ac, 6. Son Pea A” ee oe 280 ee 80, 209 | Columbella. ...... 419 534 PROCEEDINGS OF THE ACADEMY OF [1898 Galvmbids ... . suse 495 | Cylindrellide. ..... RNIN a's SS cee 207, | Gymbiola . ...._ auiaig Commelina. . .. . 387, 402 | Cymopterus ... . 29, 308 Commelinacee . 387, 393, 402 | Cynopterus. ... . 316-319 Composite 378, 383, 385, Cyperacee ..... 383, 387 391, 394, 396, 400, 408, 412 | Cyperus ...... 383, 387 Compsomyia ...... 186 | Cypripedium ...... Compsothlypis .... . SD |, Cyrena |...) eee CASI ws ey 395, 397 | Cytherea. ..... 418, 420 Conophelis: .. . 5° s jsiikae 395 | Dahlia . . 391, 394, 396, 400 Centopus. . 6 3. .'. $1, 212 | Dasyatids .- . =e 33 Convolvulacee ..... 390 |. Dasyatig’. i... sp eee ORE: «es ee 418, 462 | Dasyphora . ..: 5 Sone Cordulegaster. . .... 152 | Delphinium .... 18,286 Cordulegasterine . ... 152} Dendragapus...... Gormarem® i¢ .. 5 32's 398 | Dendrocygna. . . . 497, 498 OO ea ee ee oe 433 | Dendroica «_<,- ae 85, 217 Cartimigia © 2." 2 oie ws 379 | Dendropanax. ..... Corvus . 30, 82, 140, 212, 303 | Dentalium .. . . . 2% Coscinodiscus. . . 422. 423° Dentatia...« See 18, 293 rem as OS ae Boe a eee 172 | Diastodon . >. . Seam 22g pe en 296 | Distoma . = .... acne Craspedodiscus . ... . 423 | Dicrostonyx .-. - =n Cramatelia’. ..5.4 5 oe 419 | Diomedea .’. . = gam eT a ee 403 | Diomedeide ...... RSBEROOUR .tristian a5 24,299 | Diopside . ... .)\ceeee Crepidula . 418, 419, 435-444 | Diopsis . ....... Or) rd og eee ee ‘498 | Dioscorea ... . MEE Fs. ke sa os 19 | Dioscoreacew . . . .. ; Crocodilide ...... 101, | Diotia .: <5, +, ee CromOguerde cn tas 104 | Diplacodes. . . 3am Crocothemis ...... 153 | Diplodonta. . ... cam RpwatATIR ts. Pee 389 | Diplodus . i>... cae Crymophilus...... 138 | Diploglossus . . . . 1038, 105 Cryptochiton...... 288 | Distectria’..: -° s oumiee RC TTE = Sense ssh i 380 | Divaricella. ..: +. d,c0m Crise ys aban or Ah 396 | Dodecatheon . ... 386, 307 Gwenrnibaces.: 2 4 ik iG. 412.| Dodonwea -. +. >::) gee 9 Cee ot ne ea ak 157 | Dolichonyx « «3 foe NO sk EN eo . 157 Donita. +... .. 3. .5eee SOMME LIS ox at. ao ie 59, 60 Dosis: ce ches 419, 421 en ee eee 681 | Drymaria < . -.% Sone CDRICER cs. ge 388 | Dryobates ..... 80, 209 Cupulifers. ... . «» 395'| Duranta. . . .. + as 11 Cyanocitta. .... 82, 212 | Ectopistes ...... -» LVONODIAS 62 3) 5. ae 287 | Egregia ... . 17,47, 816 Cyclorrhynchus. ... . 128 | Eichornia. . >. 4 3 Jom 384 Cylindrella . . . 264, 267-270 | Elachiptera ......, 1898.] Eleagnus A . 40, 310 Elaphroptera . . 72-74) Emballonura . 323-325 Empidonax . 81 Endodontine . . . 221, 265 | Enyalius ... . 102, 104 Eopsepheea . ste cur ee Eostrophia . . 283 Epicrates ; . 105 Epidendrum . . 410 Epilobium . . . 405 Epinephelus : . 341 Epiphragmophora . 67-71 Epirobia. 265, 269, 272, 281 Equisetum . . 47, 314 Eretopodes acter Se Ericacez . 399, 405 Erigeron . 49, 379 Eriocaulon . . 384, 401 Eriocaulones . . 384, 401 Eriophyllum . 33, 306 Erodium . . 380, 404 Eryngium . 390, 398, 405 Eryphyla . - . 419 Erysimum . 18, 294 Erythronium . 43, 313 Esobedea . x. wl ee OOO Esochara ~ Bide IG Esocidee 340 Esox . 340 Ethalia. . 419 Eucalodium 267, 268, 270, 282-285 Euchlena . . 413 Eulima . . 419 Eulota . . 68 Eunectes . 105 Eunotia 110-118 Eupagurus = re Son Eupatorium . . 883, 408 Euphorbia 40, 311, 354, 389, 404 Euphorbiacese 389, 404 Euplectella . 430 Eupleura 418 Eupodiscus 423 Eurycarenus . 159 Eutamias 122, 123, 348- a 350, 352 | Gnathodon NATURAL SCIENCES OF PHILADELPHIA. 535 Evotomys 358-371 Exogyra 462 Exoprosopa : 158 Eysenhardtia . i 389, 393 Faleo . 80, 209 Farrea . - - 480 Festuca. ‘ 45, 314 WTOONAOIS C08 5) “a, mnt be Filices 887, 393, 400, 409 Flammulina . 221,. 222 Fragaria 403 Fragilaria . = rct elas Frasera . 36, 308 | Fratercula ee bey | Fritillaria . 44, 313 Pacis. «... % 4-20 a Fulgur . 415, 417, 418, 420 Fulica «: sa =: a eae | Fulmarus . a Gadide. . . i ee Gaillardia . 38, 306 Galeide . » « ooo Galeoscoptes . 86 Gallinula 498 Garrya . - dah AC 536 Gobiid 346 Gobius . «99, o to CUS a” at EG? Oe Gomphine. . . 20 Oe Gongylostoma 269, 271 ; 275, 276, 283 Goniothecium .* |, ae Gonolobus 411 Gouldia is , ats Gramine . . eT, a0 Grammatomya ... . 957 Graphomyia . 168 Gratiola > Fae Grindelia 33, 3806 Grus : 498 Guiraca tig 215 Gutierrezia . . . 384, 306 Habenaria . 388 Habia fg od de Eiapropoda. .: |.4%. 2) 5 bt Heematopota . 158 Halenia .' en eoe Hislia: . . . 2 RBO-192 Halizetus . fake Balictns «>... 25 BO Hamulus Hid. ads ek ee GD Harporhynchus . 86, 217 Helicarion . ; 243 Helicidz i ths, Oe Pee Helix 68,70; 107; 221 Heliornithide . .. . 495 Helminthoglypta . . . 68 Helminthophila . 216 Beploniad~ 00-35-58 a4 Hemicnemis eee Hemidactylus . 102, 105 Hemphillia 220-222, 224, 227, 230-235 Herodiones . . . 497 Hesperarion 222, 223, 226, 228, 232, 236-239 Hesperornithidee 495 Hesperornis 495 Heteractites . . . 139 Heterodactylus 101, 103, 105 Heterodonax . . 59-62 Heteroglypta. . . . . 459 Heterospermum . 383 PROCEEDINGS OF THE ACADEMY OF [1898 Heterotheca 383 Hippobosca 164 Hippoboscidee an Hippophe . . ... . Hipposideros. . . 319 Holospira. 265, 266, 272, 281-283 Hoplistomera . .- . Hoplocercus 104 Hordeum 45, 314 Houstonia uum Hyalodendron . 430-443 Hyalodiscus 423 Hyalonema 430 Hydraspis . 101 Hydromedusa . . . = ee ee . | Hyla. . : 2 Hypnum 47, 315 Hypodis . . . om Icterus . 82, 213 Rene, as! a 5 Idiostemma 270, 275, 283 Iguanide . . . . 102, 108 Hex . . . » » «nn Illecebracese . 1.) on Illyonassa . . 435, 437 Inliaculus . . . ae Tonornis me Ipomea . . 354, 390 Iridacese . 398, 402 frig... 4 eo Isarcha . . . >. « Soe Ischnochiton . . 287, 288 Ischnochitonide . .° 26% Ischnura ae 147 Stace. 2 : 83, 214 Juniperus . 46, 314, 397 JUssISA ss 4 49 Katharina . 288 Kerivoula . 321-323 Koeleria. . . . . 45, 314 Krynitskia. . . . 37, 309 Kyphoside .... . 342 Labiate . 382, 390,399, 405 Labridz ee Labrisomus ii: 5 Lagopus . 139, 140 407 «a 1898.] NATURAL SCIENCES OF PHILADELPHIA. 537 Lamourouxia . 391 | Luceilia . AO) cactat hts Rte Lanius . 216 | Lucina . 418-420, 462 Lantana 411 Lunda « L2ly «240 Laphria . . » 158 | Lunatia. 462 Laride . 131, 495 | Lupinaster . > oa ysis aloe Larus . 181, 1382 | Lupinus . 21,298, 395 Laxenecera . . » 158 | Lycodontis siti ate eee Leda. . . 419, 462 | Lynx ears.” | Legumen . . 462 | Lysine . SPE 5 Leguminaria. . 60 Lythracez . - 3, oot Leguminose 380, 388, 393, _ Lythrum * ay BOE 395, 403, 410 Mabuia. . 104-106 Leia. . . ». « + 280 | Maceo 270, 275 Leipomeles_ is . . 448 | Macha . when 1 ae Lepidopleuride . bind ae Machzerhamphus . 321 Lepidopleurus . . 287 | Maclura 41, 311 Lepidopodide - * 341 | Macoma ia eee Lepidopus . . . 341) Macroceramus 266, 280 282 Leptarionta , . . 68) Macrodontes . . 471, 472 Leptocephalide . . + 839 | Macrorhamphoside . 340 Leptocephalus . « 039 Macrorhamphosus 340 Leptocnemis . . » 142 | Mactra.. 0”. + a Leptosolen . 462 Malvacer . 381, 389, 410 Lepus . . 124) Malvastrum . 19, 294, 389 Lestes . . 147. Malvaviscus i! * 5 een Leucosticte . . 139, 213 | Mammillaria . 386 Lewisia. . . . 16,19, 295 Marcasite . 485 Lia... =... . 266, 280) Margarita . 4&6 Liatris . . 34, 306 Marsilia 383 Libellula . 143, 145, 146, 152 Marsiliacer » +, OOe Libelluline . . . 143 152 | Matricaria. 34, 306 oe adage ‘ 333 Maynardia. » . 475 Liliacer 385, 388, 397, 409 Mevachile . 55 Lilium . : 44, 49 | Megaderma 320 Limneea . . . 439 | Megascops 80 Linacez . . + » « « 404] Megaspira . 83, 284 Linum . . 19, 294, 404 Megatrigon 159, 160 Liomesus - « » + 419 Melanerpes .. . 81, 210 Lipidosternon . 104 Melanostoma . 159 Lithospermum . + 399 | Melosira 422, 423 Littorina . . . . 495, 437 | Melospiza . 84, 139, 215 kama. . . . 340 | Mentha. 390 Lobelia. . . 385, 407 | Menziesia . . 49 Lobeliacee . , . 385, 407 Merganser . * », 140 Loganiaces - » 405 | Merula . ie! 9 Claes Lomaria 47, 315 | Mesoplura . . . 59, 60,, Lonicera . 30, 303, 304 | Metastoma 282 35 PROCEEDINGS OF THE ACADEMY OF 538 Micrarionta 68 Microchloa <2 ae e foe Micronycteris . 328-330 Microseris . . 84, 306 Microsty lis pay lore eee Microtus . . 120,358 368 Middendorffa. . . . . 290 Milla : . 3885, 388 Mimosa . oY aes Se eee ee Mimulus 38, 49, 309, 407 Mimus . Oe he ae Mirabilis 379 Mischocyttarus 445 Mniotilta 85 Molothrus . 82 Monadenia. ee Sa Montia . 3. 20) "286 Mopalia . . 287, 288 Mopalliidze pee ee Morellia. 178, 175, 188 Mugilidse oy ee Mulinia 418 Mullide 341 Mullus . 341 Mureena 340 Mureenide . ; 340 Mus . : 121, 358 Musca 172, 173, 183 Muscidze 172 Muscinia = 168, 183 Mustelus Co see Bee Mychostoma . 268,272, 279 Myiarchus . ee ey ee Myodes . eh ae slite, Myospila . 168, 183 Myotis . . ; oe toed Myrtacez . i a Nassa Love 4138 Natalinse SS “Bue Natalus . . 026-328 Navicula . 110, 422, 423 Nectarina . yo ae Nectouxia . 390, 399 Nephrolepis . . 409 Nerita 202 Neritopsis . 202 Neusticurus 104 Nucifraga . 212 Nicotiana: 37, 309, 382 Nitzschia 110, 113, 114 Notholiena . a 387 Nyctaginacez . 379 Nycticeius . 321 Nycticorax . Nymphea . . 384,. 412 Nympheacee . : 384 Oceanodroma . 136 Ochromyia . ——: Odontostomus. 267, 2838, 471 (Enothera 28, 302, 378, 381, 398 Oidemia Aye 138 Oligostylus 282 Olivella . 418 Olor , 498 Onagracese 376, 381, 398, 405 Onychomys : 194 . | Ophiodes : 103, 104 | Ophiogomphus . 150-152 Orchidacese 388, 398, 409 Oreortyx . » 20s Ornithomyia - 164 Ornithorhynchus 492 Orobanchaceze 395 Oroscoptes . ae Orthetrum . . 145, 166 Orthocarpus 38, 309 Orthomesus ‘ . 202 Oryzomys . : 480, 481 Ostrea 418-420, 462 Oscinidse ; 164 Otocoris 82 Oxalis . 380, 386, 404 Oxybaphus . . | Oo, eee Oxytropis - . 16,21, 298 Pachystima 20, 296 | Pagellus . . 3842 Pagrus . 341 Palzlodus . 2) Palamedea . . 496, 497 Palamedeide . ; 497 | Pangonia . 3 ee 142,143, 152 Nucula . Nuttallia Nuttallina . Pantala . 418,419, 402 (1898. 58 288-290 1898.] NATURAL SCIENCES OF PHILADELPHIA. 539 Pantodactylus . 108, 104 | Phytolacca . . 3894 Papaveraceee . . . 379 | Phytolaccaceze a) ae ee Papuina i ee eee | Lica . 140, 212 Paracompsomyia . 169, 184 | Pineria . «oe ee Parochromyia . . 178 | Pipilo 84, 216 Parus 87, 218 | Pinna pete Ae Passer . . . 83 | Pinnulacea 381 Passerella . 139, 215 | Pinnularia ... - 110-1 18 Passeres . 489, 493 | Pinus . 46, 49, 314, 395, 397 Passerina 84, 215 | Piper . é 410 Paulicea 101, 108 | Piperacee . . 398, 410 Pecten 419, 421 | Piranga. 84, 215 Pectis : . . 9392 | Placentaceras . . . 462 Pectunculus . 462 | Placiphorella . ry pit ih joan Pedicularis 16, 38, 309, 391, 400 | Placosoma . . 108, 105 Pellea . . 393 Placuanomia . A Pentstemon . 39, 49, 309, _ Plagiobothrys 37, 3809 400, 407 Plagiogramma ot gp Peperomia . . . 398 | Plantaginacese . 383, 407 Pepsis 75 | Plantago . 383, 407 Pernettya . 399 | Platemys oi, (iy ce Perrieria . . 254 | Platophrys 347 Petalostemon . 21, 298 | Platyceras . 436 Petricola . « » « 60) Plagiodontes . 473 Petrochelidon. . . 84, 216 | Platystoma. 108 Peucedanum . . 28,302, 303 Platytrochus . 462 Phacelia . 37, 308, 309 | Plectrophenax of an Phainopepla . . 216 Pleurotoma . 190, 347 Phalacrocoracide 137 | Pliorhytis . is Sea ie oe Phalacrocorax 137 | Plumbaginacerw . . . . 390 Phalnoptilus 210 | Plumbago ; ee, Phalangium 43 | Podalirius . ~ ee, Phalaropus. . 139 Podilymbus thie, ee Phaseolus 354, 380, 388, 389 | Polemoniacee . : 382 Phellandrium . 29 Polemonium . of, 308 Phenacarion 249 Polistes . . 446-448 Philaete. . . . . . . 498. Pollenia . 169, 175 Philadelphus . . . 27, 301 | Polybia . 448-456, 458 Philibertia . - + « 890 Polychrus . - 108, 106 Philohela . 79 Polygala » 21, 297 Philomycide . . . 221 | Polygonacee . oh vy Ss, Phlox 48, 315 Polygonum 40,310, 384 Phoca ; . 200 | Polymita 68, 265 Pheenicopteride , 497 Polymyxus Marae rs Phorbia. 162 Polynices Mee toe Phyllocactus . 411 | Polypodium. . 387,400, 409° Phyllonycteris ; 333-3387 | Pomacentride .. . . 343 Physalis . 394, 406 | Pontederiacese 384 540 Toormies fo. 3. ge Popa. ce 1 0S MAR Portulacacee . 386, 388, 398, 402 Porzana ee Potentilla . . 25, 300. 403 Page. i. a) a ee Prionodactylus 101, rite 104 Procellariide . . . 135, 495 Prometheichthys . 341 Prophysaon 59)-228, 240-254 Prunella 405 tines. ~ « |.) 320; s00 Psaltriparus - RLS Psammobia . . . 957, 59-62 Psammobiide. . *° . . 57 Psammocola 59-61 Paammosolen.< 2". rr 69 Psammotella . .. .-. 58 Pseudauliscus . : 423 Pseudogryphus 208 Pseudoplatystoma 108 Pseudopyrellia ee hie Pseudo-Tsuga. . . . . 49 Psidium . Oe era Psoralea , 23; 48, 298 Pteria PA abe Pterodontia 161 Pteropus ee ae ee ei Pumas: 7’. .*..*2° ee Pugnellus . 462 Pupa. . . se Paibo Pupide . . 265, 284 Purpura ,. |e a LO Purshia. . . . » 26; 800 Putorius a a, SUL Pycnoptychia | : « BGr Bio Pygopodes. 489, 495, 497 Pyramidula eRe aa Pyrifusus 462 Pyrola . pe CD Pyrus 24,47, 299 OUCMBOUS 4. 3. ss “UN aT Quercus. . 41, 311, 388, 395 Onisonivigehs °s ws 2. ee ee Raja. . , 339 Rajide . 339 Rallus 498 PROCEEDINGS OF THE ACADEMY OF [1898. Ranunculacee 879, 885, 403 Ranunculus 379, 385, 403 Raphanus . ‘ 380 Regulus . ; 218 Reithronycteris 333-337 Reseda . : 880 Resedaceze . 3880 Rhabdonema . 468 Rhamnacee . + -SRe Rhamnus 21,266 Rhingia. : Js! Mie Rhinolophus . 319 Rhodea . 284 Rhogeéssa . 321 Rebus: ct eae ‘21, 296 Ribes «. . 27,001; 302, 398 Rissa : 131 Rosa . 26, 301 Rosacee . 408 Rosmarus . -198- 201 Rubiacese 396, 407 Rubus 26, 301 Ruellia . 391 Ruvettus . 341 Sagittaria . 383 Salicaceze 379 Salix 379 Salsola .. 875 Salvia 39, 310, 382, 399, 405 Sanguinolaria . 58-62 Santolina 3 See Sapindaceee . 389, 394 Sarcobatus . 40, 310 Saxicola . 139, 436 Saxifragacee . me | 398 Sayornis 81, 2145. 212 Scala ? 418 Scalaria . 419, 462 Scaphella 191, 192 Scaphellidze poe Schinus . 381 Schizonyx . 146 Schkubhria . 383 Scheenocaulon 409 Scienidse 342 Scincidee 104 Sciurus . ; 348 Scolecophagus 213 | . Fi 1898.] NATURAL SCIENCES OF PHILADELPHIA. 541 Scomber 341 | Sparisoma . 9 Tee mg Seat Scombride . 341 | Spartina . 46, 270, 314 Scopus . . - 497 | Spartocentrum. . ... . 282 Scorpena . . 344-346 | Spatula. ey A ee Scorpeenidse 344 | Speotyto . . . . 209, 354 Seotophilus . . 321 | Spheeralcea i a eee Scrophulariace 385, 391, Spheeroides . 344 400, 406 | Sphecodes . 56 Seutellaria . . . 39, 310) Sphyrena . 340 Sechium ~ « «+ « 412 | Sphyrenide 340 Sectilumen. . . . 271, 276 | Sphyrapicus jin Jee ee Selurus. . .. . 85, 86 -Spinus . . 83, 2138, 214 Sedum . . . . 28,302, 403 | Spirea . 26, 49, 301 Selaginella . . . . 886 | Spiranthes . += letheeiee Selasphorus . . . . . 211 | Spiroceramus. 281 Senecio 373, 392, 400, Spirostemma . 270 408, 412 | Spisula . ‘+ hae ee Sepside . . » 168.) Spizella ... . . S83e8i Sepsis . . 163 | Spondyliosoma . 342 Serranide . 341 | Squalide . 339 Serranus 341 | Stachys. 405 Sesuvium . . . « 9878 | Stauroneis . 422-497 Shepherdia . . . 40, 310 | Steganopodes . ‘ 497 Sialia . .. . . 88, 218 | Stegastes 343 Sibthorpia . . .« 406 | Stenanthium . 397 Silene 410 | Stenodermata . 333 Siliquaria . 9-61 | Stephanopyxis 423 Siphonostoma . . + « 268 | Stercorariide . . . . 130 Simorhynchus . . 128, 129 | Stercorarius . . . 130, 131 Sisymbrium Tae ey ee 133 Sisyrinchium . . . 398, 402 | Sternobrithes. . 157 Sitta . afk 86 | Stevia 392, 396, 397, 400 Smyrnium . Nh: ee ge ee ff | Solanacew 382, 390, 394, Stratiomyide . ay LOT 399, 406 Strigilla penal atiet e Solanum 382, 391, 394, Strophina 269, 271, 279 399, 400, 406 | Struthiolaria. . . . . 190 Solea 347 | Sturnella ... . 82, 218 Solecurtus . 59-61 Gubaling. «Gs 4 in, w BBA Soleide . ; 347 | Succinea 354 Solen . 59, 61, 62, 418 | Surirella 110 Solenoglyphe . 108 | Swertia . 36 Solidago . 34, 1, 306, 385 | Sylvania 86 Somalia . 181 Sympetrum eer eee Somateria . 138 | Symphoricarpos . . 49, 400 Sophora . » « « 854 | Synodontide . . .. . 840° Sorbus - + « « « 47, 315 | Synodus 340 Sparide .... . . 3841 | Syneca. 446 542 oo 39, 310 Syrians hw es 80 Byrne: ox... . Sayer 159 PIS sg! x owe nee 159 sy NE Se eae 157 MBDBRUS so gee PS . 168 SS es Dart 470 Tachycineta ... . 84, 216 MABON ng as ye te 59-62 Tagetes . 391, 392 Talinum . 386, 388, 412 RINGS sb ie 123,436 A sd Sy 8 a te, 28 457 Pawodinm 56.0 5 AMO 413 Tesenid 4o.3. ote 386 to a 103, 108 Telephoromyia .... . 74 Soming cS xy 62, 418, 429 Testudinids : 101 CMOS. Gh) a Ge 101 SGN teak iyié 195 Tetraodontide . 344 Thalossoma. . 343 Thalia! .: ia Thalictrum. .. a) “403 Thanmass «i... 268, 270 Turyothoras 3027. 2 ).°% 217 BB BOR as. . SSG 12 oe a ce hr eG Tomelasmus 271, 276 $0 eS as 283 TOrmGUnh «sic <. . 418 Tonicella 287 (Te cs 139 Toxifera . 190 Preacher. 0% i Se 269 Trachinide . 346 Trachinus 346 Traenere: sss cys Sb 341 Trachydermon 287, 290 Tradescantia .. . 393, 402 Ji ee en 143, 144 Triceratium ...... 423 Trichechus. ... . 196, 197 ‘Prichotropia . 25 G'6 462 Trifolium 24, 299, 380, 403, 404 Bgl! ee a ree 347 Triglide ‘ee ee 347 [1898 TEMPOWIA > és

; = <2e8 321 |) PyTaNNUs: 2) Seas 81, 211 | Umbellifere . . 390, 398, 405 Umbrina 5... 5 .. e 342 Cot ee ese 129, 140 Urinator. .. . =) .i.)ee 126 Urinatores.. . .... 2m 495 | Urinatoridss, .... a: ae 126 Urocoptids. . ... am 476 Urocoptis 267, 270, 273, 281, 282 Urophycis. 4...) |e 347 Vrosalpins: 4) 417, 418 Urostrophus 102, 104 Urticacese ; ») ae Vaccinium . . 36, 307 Veleda; 4. os. «1%, Gea 462 Vendrysia . 280 Veniolla..a7 +. Jasco 462 VWoonus 0) >. f a5' 8 418 Veratrum 44, 313 Verbenaceze . . 890, 411 Vespertilio. . : . 27 321 Veaperus .) 6 .(4.. 5) ae 321 | Viburnum . 482-484 Viola ..a +. oe 405. Violseew ji 6. 5 eee 405 VaRees sce pepwe « 84, 85, 216 Volutacea® » s<'s+ Ae 191 Volutide...... +.4 .. +98 192 Volutomitra . . . . 191, 192 Fae on Le » » 402 Weldenia 1898.] NATURAL SCIENCES OF PHILADELPHIA. 543 jp Ct a ar as aio: |. Zeoxmenia. 290) 6. tg 392 PRONE) i 2, saad, cao | Bindla ou fe as 392 NE 68! Pe ag, oh UY 132 | Zizania ...... 46, 314 seononiens 2°) is. a Set Zomabes: 9s 5-515. es Oe 67 Xerophyllum. . . . 44, 313 | Zonochroa. ...... 178 Pees See Sh A Te 419 | Zonotrichia. ... . 139, 214 Mamelodia . <°.+. 9... Oa ee 388, 393 a?) ah i eae he 413 | Zygadenus.... . 45, 313 Zenaidura . . . 79, 208, 354 | yo a aa Rae 146 544 PROCEEDINGS OF THE ACADEMY OF (1898. GENERAL INDEX. Allen, Harrison M. D. and George H. Horn, M. D., pro- ceedings of a meeting held in commemoration of, 11. Arnold, Crawford, ment of death of, 11. Barber, C. M. and T. D. A. Cock- | from | 9; _ Conchological Section, report of erell. A new weasel New Mexico, 89, 188. Barr, Martin W., M.D. Idiocy, educationally, 89. Bascom, Florence. Petrographic methods of rock determination, 488. Biological and Microscopical Sec- tion, report of the, 512. Botanical Section, report of the | 515. Boyer, C.S. Some new species of diatoms (Plate XXIV), 262, 468. Report of the Bio- | logical and Microscopical] Sec- tion, 512. Brinton, Daniel G., M.D. The | ethnology of the Philippines, 467. Report of Professor of Ethnology, 519. Brown, Stewardson. the Botanical Section, 515. Calvert, Philip P. Odonata (Dragonflies) from the Indian | Ocean and from Kashmir, col- lected by Dr. W. L. Abbott, | 141. The radula in the squid, 202. Chapman, Henry ©. M. D. Notes on the squid, 202. Re- port of Curators, 509. announce- | Report of 1898. Cockerell, T. D. A. New and little-known bees from Wash- ington State, 50. Committee on Hayden Memorial Award, appointment of, 205. Report of, 338. ree a Standing, for 1898, the, 513. Conklin, E. G. Environmental and sexual dimorphism in Crepidula(Plates X XI, XXII, | XXITT), 262, 435. Cope, Francis R. The summer _ birds of Susquehanna Co., Penna., 9, 76. _ Corresponding Secretary, report of, 504. Coues, Elliott, M.D. Notes on Mr. Meehan’s paper on the plants of Lewis and Clark’s Expedition across the conti- nent, 1804-06, 262, 291. Council and Standing Commit- tees for 1899, 520. Crosse, J. C. H., announcement of death of, 429. Curators, report of, 509. Dall, William H. Synopsis of recent and tertiary Psammobi- idee of North America, 57. On the genus Halia of Risso, 89, 190. DeCamp, Wm. H., announce- ment of death of, 429. _ Elections during 1898, 521. =. on i eee as 1898.] Entomological Section, report of the, 514. Fox, William, J. Contributions to a knowledge of the Hymen- optera of Brazil, No.4. Thyn- nine and additions, 9, 72. Contributions to a knowledge of the Hymeneptera of Brazil, No. 5. Vespide, 429, 445. Synopsis of the United States species of the hymenopterous genus Centris Fabr., 488. Frazer, Dr. Persifor. Glimpses of Russia in Europe, Asia and Asia Minor, 11. General Index, 544. Goldsmith, E. Volcanic rocks of Mesozoic age in Pennsyl- vania, (Plates II, III, 1V, V), 90. The petrifaction of fossil bones, 98. Hall, James, announcement of death of, 357. Hamilton, S. Harbert. The occurrence of Marcasite in the Raritan formation of N. J., 479, 485. Harshberger, J. W., M. D, Bo- tanical observations on the Mexican flora a on the flora of the Valley of Mex- ico, 263, 372. Heilprin, Angelo. Geology and physical geography of the Klondike Gold Mining Region, 488. Hough, Garry de N.,M. D. The Muscide collected by Dr. Donaldson Smith in Somali- land, 155, 165. Index to Genera, etc., 531. James, J. Wharton. Enchanted Mesa, 467. Jefferis, Wm. W., a as Curator of the \ Vaux collections, 205. Report on William 8. Vaux collee- tions, 512. The NATURAL SCIENCES OF PHILADELPHIA. —— — 545 Johnson, Charles W. Diptera collected by Dr. A. Donald- son Smith in Somaliland, East- ern Africa, 157. New cretace- ous fossils from an artesian well-boring at Mount Laurel, N. J., 429, 461. Jordan, David Starr and James Alexander Gunn, Jr. List of fishes collected at the Canary Islands by Mr. O. F. Cook, with descriptions of four new species, 338, 339. Judson, Oliver A., M. D., an- nouncement of death of, 202. Keller, Ida A. Notes on the growth of Viburnum lantan- oides (Plate X XV), 479, 482. Letson, E. J. Description of a new Tethys (Aplesia), (Plate VIII), 89, 193. Libbey, William, Jr. The En- chanted Mesa, 467. Librarian, report of, 505. McKean, Thomas, announcement of death of, 155. ‘ Marcou, Jules, announcement of death of, 338. Meehan, Thomas. The plants of Lewis and Clark’s expedition across the continent, 1804— 1806,12. Report of the Botan- ical Section, 515. Mercer, Henry C. The bone cave at Port Kennedy and its par- tial examination in 1894, 1895 and 1896, 479. Merriam, C. Hart. Description of three new rodents from the Olympic Mountains, Washing- ton, 351, 352. | Miller, Gerrit S., Jr. List of bats intment | “illlam 8. | collected by Dr. W.S. Abbott in Siam, 262,316. Descriptions of five new Phyllostome bats 262, 326. A new Chipmunk from Northeastern China, 338, 348. Descriptions of a new 546 PROCEEDINGS OF THE ACADEMY OF genus and species of Microtine | rodent from Siberia, 357, 368. Notes on the Arctic Red- backed mice, 357, 358. Mills, Chas. K., M. D. physiologically, 89. Mineralogical and Geological Section, report of the, 517. Moore, Clarence B. Certain ab- original mounds of the South Carolina coast, 262, 263. Cer- tain aborignal mounds of the Savannah River, 262, 268. Certain aboriginal mounds of the Altamaha River, 262, 263. Recent acquisitions, 262, 263. Moore, J. Perey. Hyalodendron navalium, a new genus and species of Euplectillid sponge (Plate XIX, XX), 338, 430. Morris, Charles. On the antiquity of man from the standpoint of evolution, 263. Nolan, Edw. J., M.D. A memo- rial of Dr. Joseph Leidy, 465. Report of RecordingSecretary, 500. Report of Librarian, 505. Officers, Councillors and Finance Committee for 1899, 520. Ornithological Section, report of the, 518. Palmer, T. Chalkley. Errant frustules of Eunotia major, (Plates VI, VII), 89, 110. Perot, Charles P., announcement of death of, and memorial min- ute, 479. Pilsbry, Henry A. The function of the radula, 202. Chitons collected by Dr. Harold Heath at Pacific Grove, near Mon- terey, Cal., 262, 287. A new land snail from Clarion Island, 351, 354. New species of Odon- tostomus from Brazil and Argentina, 429, 471. Margar- ita Sharpii, a new Alaskan gastropod, 479, 486. Report Idiocy, [1898. of the Conchological Section, 513. Report of Professor in Department of Mollusea, 519. Pilsbry, H. A. andE. G. Vanatta. Anatomical notes on certain West American Helices, (Plate I), 67. Revision of the North American slugs: Bin- neya, Hemphillia, Hespera- rion, Prophysaon and Anaden- ulus. (Plates IX, X, XI, XI1, XIII, XIV, XV, XVI), 156, 219. Material toward a natural classification of the Cylindrelloid snails (Plates XVII, XVIII), 203, 264. Some Cuban species of Cerion, 465, 475. Rand, Theodore D. The Birds- boro trap quarries, 10. Report of the Mineralogical and Geo- logical Section, 517. Recording Secretary, report of, 500. Report of Biological and Micro- scopical Section, 512. Report of the Botanical Section, 515. Report of the Conchological Sec- tion, 513. Report of Corresponding Secre- tary, 504 Report of Curators, 509. Report of the Entomological See- tion, 514. Report of Librarian, 505. Report of the Mineralogical and Geological Section, 517. Report of the Ornithological Sec- . tion, 518. Report of Recording Secretary, 500. | Report on William S. Vaux Collections, 512. Reports of the Professors, 519. Rhoads, Samuel N. On a small collection of mammals from Northeastern China, 11, 120. 1898.] A new grasshopper mouse from New Mexico, 155, 194. Notes on the fossil walrus of Eastern North America, 155, 196. Sandberger, Fridolin, announce- ment of death of, 338. NATURAL SCIENCES OF PHILADELPHIA. 547 Southern New Jersey, 480. Report of the Ornithological Section, 518. Torell, Otto Martin, reception of Hayden Memorial Award, 338. Biographical notice of, 355. Seale, Alvin. Notes on Alaskan | Valentine, John K., announce- Water Birds, 11, 126. Shallcross, John, announcement of death of, 479. Sharp, Benjamin, M. D. Rock inscriptions in Kauai, Hawai- | ian Islands, 203. Report of Corresponding Secretary, 504. Shufeldt, R. W., M. D. Some observations on the classifica- tion of birds, 480, 489. Singerly, Wm. M., announcement of death of, 155. Skinner, Henry, M.D. Report of the Entomological Section, | 514. Report of Professor in Department of Insecta, 519. Spiller, Wm. G., M. D. Idiocy, anatomically, 89. Stone, Witmer. On the breeding | habits of birds of Eastern Pennsylvania, 155. A study of the type specimens of birds in the collection of the Academy | of Natural Sciences of Phila- delphia, with a brief history of | the collection, 480. Occur- rence of Oryzomys palustris in ment of death of, 11. Van Denburgh, John. The Ger- rhonotus of the San Lucan fauna, Lower California, with diagnosis of other West Amer- ican species, 63. Birds ob- served in Central California in the summer of 1893, 156, 206. Vaux, J. Waln, announcement of death of, 262. Von Ihering, Dr. H. Contribu- tions to the herpetology of Sao Paulo, Brazil.—I, 101. Warner, Redwood F., announce- ment of death of, 488. _ Wernwag, Theodore, announce- ment of death of, 262. | William S. Vaux Collections, report on, 512. Witmer, Lightner. physiologically, 89. Woolman, Lewis and Charles S. Boyer. Fossil mollusks and diatoms beneath the Dismal Swamp, Virginia and North Carolina. With notes on the diatoms, 11, 414. Idiocy, ** ” PROC. ACAD. NAT. SCI. PHILA. 1898. PLATE I. PILSBRY AND VANATTA. ANATOMY OF HELICIDA. we Thy a SEAS Ff 4 tw, » og PALMER Ss MOVEMENTS OF PLATE VI. rm PROC. ACAD. NAT. SCI. PHILA. 1898. PLATE Vil. <2; = + 4 PALMER. MOVEMENTS OF EUNOTIA PLATE VIII PROC. ACAD. NAT. SCI. PHILA. 1898. ne 2 TETHYS PILSBRYI terson. nm e « \ Les VG Z- PROC. ACAD. NAT. SCI. PHILA. 1895. PLATE IX. + Sia Seo stn fis Ws © loss Ps Pilsbry and Vanatta del. PILSBRY AND VANATTA. NORTH AMERICAN SLUGS, Pilshbry and Vanatta del. PROC. ACAD. NAT. SCI. PHILA. 1898. PLATE SSE ; Mu paw eT TD ° ~ i a) . mi “* PROC. ACAD. NAT. SCI. PHILA. 1898. PLATE XXIV. BOYER ON DIATOMS PROC. ACAD. NAT. SCI. PHILA. 1898. PLATE XXV. KELLER ON VIBURNUM LANTANOIDES. QH Aeademy of Natural Sciences 1 of Philadelphia A2 Proceedings v.50 Biological & Medical Serials PLEASE DO NOT REMOVE CARDS OR SLIPS FROM THIS POCKET UNIVERSITY OF TORONTO LIBRARY HOPNONQOH ARNO NAAN AAAS SAS RAN OAD DIMNY