PROCEEDINGS ACADEMY OF NATURAL SCIENCES PHILADELPHIA. 1893. COMMITTEE ON PUBLICATION. John H. Redfield, Edward J. Nolan, M. D. , Thomas Meehan, Charles E. Smith, George H, Horn, M. D. Editor: EinVARD J. NOLAN, M. D. *-" ''^'' PHILADELPHIA : ACADEMY OF NATURAL SCIENCE.^, LOGAN SQUARE, 1894. 39 Academy of Natural Sciences ok Philadelphia, March 29, 1894 I hereby certify that copies of the Proceedings for 1893 have been presented at the meetings of the Academy as follows : — ^es 9 to 56 " 57 to 72 " 73 to 120 " 121 to 168 " 169 to 200 " 201 to 216 " 217 to 232 " 233 to 312 '■ 313 to 344 " 345 to 360 " 361 to 376 " 377 to 424 " 425 to 456 " 457 to 520 " 521 to 552 March :SIarch March April April May July September October October December January February' ISIarch March 1893. 1893. 1893. 1893. 1893. 1893. 1893. 1893. 1893. 1893. 1893. 1894. 1894. 1894. 1894. I f}SL K U6 EDWARD J. NOLAN, Recording Secretary. I'RI\T(;l?^ AMI FNCiRAVERS, PHILA. LIST OF CONTRIBUTORS. With reference to ttie several articles contributed by each. For Verbal Comniunicatious see General Index. Brown, Arthur Erwiu. Notes on some Snakes from Tropical America lately living in the Collection of the Zoological Society of Philadelphia 429 Calvert, Philip P. The Odonate genus Ortholestes 377 Chapman, Henry C, JM. D. The interpretation of certain verses of the First Chapter of Genesis in the light of paleontology 68 Notes on Choeropsis liberiensis (Morton) (Plate IV) . . ; . . 185 Observations on the Japanese Salamander, Cryptobranchus maximus (Schlegel) (Plates V, VI and VII) 227 Chapman, Henry C, M. D. and Albert?. Brubaker, M. D. The radius of curvatures of the Cornea 349 Cope, Edward I). A new extinct species of Cyprinidae 19 A contribution to the herpetology of British Columbia . . . 181 Description of a lower jaw of Tetrabelodon Shepardii Leid^-. 202 On a collection of Batrachia and Eeptilia from southwest Missouri 383 On the Batrachia and Reptilia of the Plains at Latitude 36° 30' 386 Geographic variations in Bassariscus astutus, with descrip- tion of a new subspecies 413 Dall, W. H. The phj'logeny of the Doeoglossa 285 Dixon, Samuel G., M. D. Involution form of the Tubercle Bacil- lus and the eflect of subcutaneous injection of organic sub- stances on inflammations 100 Ellis, J. B. and B. il. Everhart. New species of North Ameri- can Fungi from various localities 128 New species of Fungi from various localities 440 Fox, "William J, The North American Larrida? 467 Goldsmith, E. Notes on some minerals and rocks (Plates I and II) 174 A tempered steel meteorite (Plate IX) 373 Keller, Ida A. The glandular hairs of Brasenia peltata Pursh (Plate III) 188 Meehan, Thomas. Contributions to the life histories of plants. No. 9 289 Meehan, William E. A contribution to the flora of Greenland . 205 Meyer, Abraham. Notes on the occurrence of quartz and other minerals in the Chemung Measures, near the line of Ly- coming and Tioga Counties, Pennsylvania 194 Pyrophyllite slate in Northern Pennsylvania 197 Moore, J. Percy. On some Leech-like parasites of American Crayfishes (Plate XII) 419 Kex, George A., M. D. New North American Myxomycetes . . 364 Khoads, Samuel R. The birds observed in British Columbia and Washington during the spring and summer, 1892 21 Description of new species of North American .Mammals with remarks on species of the genus Perognathus 404 Ryder, John A. The inheritance of modifications due to distur- bances of the earlj' stage of development, especially in the Japanese domesticated races of Gold-Carp 75 The vascular respiratory mechanism of the vertical fins of the viviparous Embiotocidpe 95 Sharp, Benjamin, M. D. Catalogue of the Crustaceans in the Museum of the Academy of Natural Sciences of Philadel- phia 104 Sterki, V. Observations on Vallouia (Plate VIII) 234 Growth changes in the radula in Laud Mollusks (Plates X, XI) 388 Stone, Witmer. Description of a new species of Neotoma from Pennsylvania 16 Strecker, Herman. Descriptions of two new species of North American Bombycid^e 282 Tarr, Ralphs. Notes on the physical geography t>f Texas . . . 313 PROCEEDINGS ACADEMY OF NATURAL SCIENCES PHILADELPHIA. 189: January 3. The President, General Isaac J. Wistar, in the chair. Sixty-three persons present. A paper entitled " The Interpretation of Certain Verses of the First Chapter of Genesis in the Light of Paleontology," by Henry C. Chapman, M. D., was presented for publication. The Council reported that the following Standing Committees had been appointed to serve during the ensuing year: — On Library. — W. S. W. Ruschenberger, M. D., Henry C. Chapman, M. D., Gavin W. Hart, Charles P. Perot and J. Bernard Brinton, M. D. On Publications. — John H. Redfield, Charles E. Smith, Thomas Meehan, George H. Horn, M. D., and Edward J. Nolan, M. D. On Instruction and Lectures. — Charles Morris, Isaac C. Martindale, Harold Wingate, George A. Rex, M. D., and J. Bernard Brinton, M. D. Standing Committee of Council on By-Laws. — W. S. W. Ruschenberger, M. D., Theo. D. Rand, William Sellers and Isaac J. Wistar. 2 10 PROCEEDINGS OF THE ACADEMY OF [1893. The deaths of AVm. S. Pine, a member and P. R. Hoy, a cor- respondent, were announced. The death on the .3rd inst. of Isaac C. Martindale, the Treasurer of the Academy, having been announced the following minute was adopted : — The Academy of Natural Sciences of Philadelphia, in view of the sudden death of Mr. Isaac C. Martindale, its late Treasurer, expresses its profound regret thereat, and records its sense of the great service rendered by him in the faithful, laborious and efficient discharge of his duties as custodian of the Academy's funds. As a naturalist Mr. Martindale won the confidence and respect of his fellow Academicians. He was regarded as one of the best analytical botanists in the United States. His knowledge of special American, European and Australian floras was very exact and wide. His herbarium was one of the standard collections of the country, frequently consulted by students of plants and always generously placed at the service of his fellow botanists. As an entomologist he had acquired a good knowledge and a valuable collection of Lepidoptera. At his death he was the Vice? President of the American Entomological Society and Ento- mological Section of the Academy. Mr. Martindale's relations to his associates were always most pleasant and helpful. His invariable courtesy, willingness to aid his fellow naturalists and his unselfish interest in the advancement of science and especially the prosperity of the Academy are here most cordially recognized and recorded. Metumorplmm of Sedimentary Rock.^. — Mr. Jos. Willcox stated that he had observed an example of the metamorphism of sedi- mentary deposits into crystalline rocks on an island in Rideau Lake, Canada, about 40 miles north of Alexandria Bay. At this locality the Laurentian granite is covered by gneiss rocks which in some cases appear like a coarse granite containing cleavable feldspar as large as an egg. The sedimentary origin of these gneiss rocks is indicated by many enclosed, smooth, round quartz pebbles some of which are more than two inches in diameter. January 10. The President, General Isaac J. Wistar, in the chair. Forty persons present. Papers under the following titles were presented for publication : — 1893.] NATURAL SCIENCES OF PHILADELPHIA. 11 " On a now extinct species of Cyprinid?e," by Edw. D. Cope. "On the Inheritance of ^lodifications due to the Disturbance of the Early Stage of Development in the Japanese Domesticated Races of Gold Carp," by John A. Ryder. " The Vascular Respiratory ]\Iechanisni of the Vertical Fins in the Viviparous Embiotocidse," by John A. Ryder. January 17. The President, General Isaac J. AVistar, in the chair. Fifty-three persons present. Papers under the following titles were presented for publication : — " Catalogue of the Crustaceans in the Museum of the Academy of Natural Sciences of Philadelphia," by Benjamin Sharp, M. D. " Description of a New Species of Neotonia," by Witmer Stone. Mr. Chas. p. Perot was elected Treasurer to fill the vacancy caused by the death of Mr. Isaac C. Martindale. January- 24. The President, General Isaac J. Wistar, in the chair. Fifty-nine persons present. A paper entitled " New Species of North American Fungi from various localities," by J. B. Ellis and B. i\I. Everhart, was presented for publication. The deaths of Dr. J. S. Newberry and Sir Richard Owen, corres- pondents, were announced. The Forms of Edentulous Jmvs in the Human Subject. — Dr. Har- rison Allen demonstrated the peculiarities of the edentulous upper and lower jaws of the human subject. He held that the statement made that the jaws exhibit the result of uniform absorp- tion of the alveolar processes was not true. The bone tissue which held the teeth in place being a complemental structure is indeed rapidly absorbed after the teeth are lost. But when the alveolar processes have disappeared, a secondary process of adaptive hyperos- tosis takes place. These statements relate in the main to the upper jaw, but the conclusions can be applied also to the lower jaw. This adaptive process occurs in three regions, namely, that for the incisor teeth, that for the canine tooth and the first bicuspid tooth, and that for the second bicuspid tooth and the molar teeth. These 12 PROCEEDINGS OF THE ACADEMY OF [1893. regions answer roughly to those occupied by various kinds of teeth, and differ in much the same way as the incisiform, caniniform and molariform teeth differ from one another. The region of the incisor teeth is compressed and beaked, that of the canine tooth and the first bicuspid tooth is coarsely conical or tubercular, while that of the second bicuspid and molar teeth is either broad and massive, or compressed. It is rare to find an edentulous dental arch uni- formly hyperostosed or uniformly atrophied, but one or more of the regions above named assume the form described, or at least exhibit indications of changes different in character from the mere loss of the alveolar processes. The lower jaw passes up in front of the upper jaw in aged individ- uals who have lost teeth. As a result, the attrition of the incisorial region of the lower jaw is secured against the front of the upper jaw. The result attained by such attrition Dr. Allen called "shearing." Shearing takes place in proportion as the upper jaw at its anterior arc is beaked. It is interesting to find that when "shearing "is present the articular surface of the condyloid process is invariably at the anterior part. The loss of the alveolar process in the incisorial region of the upper jaw causes the incisive foramen to assume an absolutely new position in relation to the line of mastication. It exhibits a dispo- sition to lie in the dental arch instead of back of it. The attri- tion by "shearing" however, protects the contents of the foramen from pressure. The region in the upper alveolar arch directly back of the last molar is apt to become symmetrically hyperostosed. These masses appear to be dominated by the pyramidal process of the palatal bones and the pterygoid process of the sphenoid bone. At least they are not used for mastication. The subdivision of the teeth into kinds, which answer to the incisors, canines, bicuspids and molars, correlates to the strongest suture lines in the face, that is to say, the incisors correspond to the premaxillo-vomerine junction, the canine and first bicuspid to the fronto-maxillaryjunction, and the remaining teeth to the fronto-raalar junction. The edentulous skulls examined were 14 in number, distributed as follows; Ancient Egyptian, 3; Arabian, 2; Hindu, 2; Peru- vian, 2 ; Negro, 1 ; X. A. Indian, 2 ; Anglo-American, 2. Of this number the Anglo-Americans alone could by any possibility repre- sent the teeth of persons who could have worn artifical teeth, and in this way modify^ the act of mastication in the aged. Since one of the Anglo-American crania was that of an idiot, the probability is reduced to a minimum that an artificial denture had been used during life in any of the specimens examined. 1893.] NATURAL SCIENCKS OF PHILADELPHIA. 13 f Entire arch hyperostosed, 3. \ Enlire arch absorbed, 4. ( Left side arch hj'perostosed, ]. { Right side arch liyperos'osed, 0. ( Left side arch absorbed, 2. \ Right side arch absorbed, 4. Region of incisors hyperostosed (" beaked "), 6. Region of incisors " sheared, 5. f r Right and Left, 2 I Region of canine and first bi-cuspid hyperostosed-^ Left, 1 J ' (Right, 1 1 r Right and Left, 2 I Region of canine and first bi-cuspid absorbed < Left, 0 L i Right, 0 r> • r J u- -J J r Riijht and Left, 2. Region of second bicuspid and 1 t 7. i molars h)perostosed J ,^ / -.' T> • r J 1 • • 1 J ( Riijlit and Left, 0- Region of second bicuspid and 1 i r, i molars absorbed 1 ,,. ,' ,," I Right, 2. 13 • r J u- J J f Right and Left, Region of second bicuspid and 1 , ^^ molars " beaked " J „. ,' ,,' (^ Right, (). Symmetrical hyperostoses in alveolar arch in front of pterygoid process 8. Incisive foramen in hne of dental arch 8. It is noteworthy that from the entire series only four showed com- plete absence of any secondary bone adaptation consequent upon the loss of alveolar processes, and that all of these were from civil- ized races, two ancient Egyptian and two Anglo-American. The want of harmony between the secondary adaptations probably cor- relates with the irregular rate at which the teeth are lost. Individ- ual peculiarities in this regard are doubtless numerous. Dr. Allen assumed that the coarse food of savage and semi-savage people caused the jaws even in an edentulous condition to be used actively in the act of mastication, while the more carefully prepared food suitable to the aged of civilized people enabled the jaws to have comparative rest, and hence the mechanical conditions which pre- determined the localization of new structures were not active. The speaker concluded that the series of observations strengthens the position taken that the same forces which differentiate the kind of teeth operate in fashioning the shape of the jaws, even after the loss of the teeth. Dr. C. N. Pierce remarked that the four superior arches, which Doctor Allen has presented as being representatives of civilized races, could not be accepted as indicating a uniform condition of edentulous jaws at the present time. The crania collected from civilized communities in the ftiture will, in their edentulous jaws, certainly show less irregularity in the individual alveolar ridges than was present in the several specimens exhibited by Dr. Allen, and in the absence or ))resence of a ridge would not 14 PROCKEDINGS OF THE ACADEMY OF [1893. display the iinitbrmity seen in the four exhibited. In the future, the greatest variations will certainly be exhibited. In some a prom- inence will be present, which in life amounted to almost a monstros- ity, while in others there will be found a complete atrophy or absorption of the entire ridge in both the superior and inferior maxilla. The symmetry of the ridge will in a measure be due to the uniformity of pressure from an artificial denture, and an absence of the forces alluded to by Dr. Allen, which doubtless had had in some cases an influence in the secondary development of bony structure, while those parts were forced to perform the function of the teeth which had been prematurely lost, though some of the prominences to which attention had been drawn, were, in the estimation of Dr. Pierce, due to the diflTerence in the time of the loss of the teeth. Why some maxillaries should show such complete atrophy, while others had secondary development, Dr. Pierce could not explain, but he believed it was associated with temperamental and nutritional conditions. The development certainly indicated a healthy recupera- tive power on the part of the individual. With reference to the protrusion of the lower jaw and chin, and the change in adaptation of condyle to glenoid cavity, which Dr. Allen had so aptly illustrated. Dr. Pierce thought they could be explained upon the principle of use and disuse, with adaptation of structures. In infancy, the angle resulting from the relation of the ramus to the body of the bone was much greater than a right angle, indeed the ramus was but little above the same horizontal plane occupied by the body of the bone, and the jaw was capable only of vertical and antero- posterior motion, such as is essential to sucking or nursing. As the three true or permanent molars are developed, the ramus assumes its vertical position, forming almost a right angle with the body of the bone, and at the same time making lateral or horizontal movement possible while establishing the concomitant relation between the condyles and glenoid cavities. As these permanent molars later in life are lost, the force upon the jaw in occlusion is confined to the anterior part or incisive locality, which would necessarily tend to increase the angle and protrude the chin. This occurs sometimes quite early in life and while all the anterior teeth are in position. At the same time that the vertical motion is exerting this influence the necessity for lateral motion has ceased, by the loss of the grinders; hence the change in the relative position of the condyle, which was so well shown by the previous speaker, and which has been necessitated by a return to the vertical and anteroposterior motion common to infancy, with the loss of the horizontal or lateral motion of maturity. In consequence of his election to the office of Treasurer, Mr. Chas. P. Perot resigned from the Finance Committee. Dr. Geo. H. Horn was elected to fill the vacancy. 1893.] natural sciences of philadelphia. 15 January 31. The President, General Isaac J. AVistar, in the chair. One hundred and one persons present. The deaths of Nicholas Koksharow and Axel Gadoliu, corre- spondents, were announced. Mr. Thomas A. Robinson was elected to fill a vacancy in the Council caused by the ex-officio membership therein of Mr. Chas. P. Perot. The following were elected members : — Geo. M. Warren, Nelson H. Strong, Norris J. Scott, Thomas Say Speakman, Clarence B. Moore, Mary K. Gibson, Jr., J. Howard Gibson, Thomas Bradley, Edwin Greble Dreer, Richard C. Schiedt, Charles N. B. Camac, Wm. Evans Wood, John C. Sims, William D. Winsor, Clarence B. Newbold, Wm. H. Joyce, Alexander J. Cassatt, Samuel F. Houston, Alexander E. Harvey, Charles Hacker, Edw. A. Buckley, Jr., Mark T. Patterson, Geo. B. Heckel, Benjamin W. Richards, Eugene Delano, Malcolm Lloyd, Charles H. Banes, Theodore C. Search, William H. Ingham and Algernon Sydney Logan. The following were elected correspondents : — William Libbey, Jr. of Princeton, N. J., Alfred Russell Wallace of London, G. B., and G. H. Theodor Eimer of Tubingen, Germany. The following were ordered to be printed : — 16 proceedings of the academy of [1893. description of a new species of neotoma from pennsylvania. By Witmer Stone. I have recently obtained through the kindness of Mr. J. G. Dillin two specimens of a Avood rat which were secured near the top of South Mountain (2,000 ft.), Cumberland County, Penna., some six miles from Pine Grove, at u point known as Lewis's Cave, which constitute the first record of the occurrence of the genus Neotoma in this State. The first specimen of this rat secured by Mr. Dillin was a male, and was taken in a trap set for raccoons. It was at once rec- ognized as different from the common brown rat, and was preserved with a view to having its identity settled, but was afterward unfor- tunately lost. The next day, Dec. 2, 1892, a female specimen was secured and was brought to me in the flesh. At my request INIr. Dillin wrote to friends who were hunting on South Mountain and secured one more specimen. After comparing these two specimens with a series of Neotomas from the collection of the American Museum of Natural History kindly loaned me by Mr. F. M. Chapman and some specimens loaned by Dr. C. Hart Merriam, of the U. S. Department of Agri- culture, I am convinced that they represent an undescribed species, for which I propose the name of Neotoma pennsylvanica. This species may be distinguished from N. floridana of the South Atlantic and Gulf States by its larger size, its densely hairy and distinctly bicolored tail and by certain well marked cranial charac- ters. The specimens here described are both females, and are perhaps not quite full sized, though evidently adult. The male specimen, according to Mr. Dillin's account, must have been at least twenty inches (508 mm.) long, and had the tail more hairy than the two in my possession. The detailed description follows : Neotoma pennsylvanica sp. iiov. Pennsylvania Wood Rat. Type No. 156 Collection of Witmer Stone, 9 South Mountain, Cumberland County, Penna., Dec. 2, 1892. J. G. Dillin. General color similar to that of N. floridana, plumbeous above with a number of black hairs interspersed and a yellowish brown Tail (Vert). Hind Foot. mm. mm. 185 41 190 43 1898.] NATURAL SCIENCES OF PHILADELPHIA. 17 undertone which is pure and bright on the sides of the head and body, becoming almost a pinkish tint on the flanks. Feet and lower surface pure white. Tail densely hairy, surpassing in this respect any specimens of either N. floridana or N. mexieana that I have seen. The color of the tail is black above and pure white beneath, the line of demarc- ation being very sharp ; viewed from directly above, the scales are completely hidden by the hairs. The two females in my possession measure as follows : Length, mm. No. 1.56, Collection W. S 403 No. 1.57, " " 416 Comparing the skull of N. pennsylvanica with that of N. floridana we find it larger and proportionately longer and narrower. The upper surface is more nearly horizontal {i. e. not so much curved), the frontal bones are much depressed along the frontal suture, the outer edges next to the orbits forming decided ridges. The ptery- goid processes are larger and converge more than in N. floridana, so that the meso-pterygoid fossa is longer and narrower. The upper margin of the infra-orbital foramen as viewed from above is also much narrower in N. pennsylvanica. The teeth are rather heavier than in N. floridana, and the distance between the anterior molar and the incisor (from the alveolse) is relatively greater. A table of cranial measurements follows, the measurements of a male (No. 1,129) and female (No. 1,127) N. floridana from Gaines- ville, Florida, Amer. Mas. Nat. Hist, collection, being given for comparison : — 18 PROCEEDINGS OF THE ACADEMY OF N. pennsyl- vanica. Coll. W. Stone No. 157. No. 1.56 Occipito-nasal length 53 — Basilar length (from foramen magnum to incisor). 449 54 Zygomatic breadth 27 27 Mastoid breadth 20 6 20 Interorbital constriction 7 66 Length of nasals 20 21 Foramen magnum to incisive foramen 31 — Foramen magnum to palate 20"6 i — Length of upper molar series (on alveolcc) 9*8 10 Length of incisive foramen 10 106 Length of mandible (symphysis to angle) 30'5 30 I << " " (symphysis to condyle) ' 322' 31 Coronoid process from angle 153 14'5 Ratios to Basilar Length. Zygomatic breadth 60*1 j Mastoid breadth 45*9 j Nasals 44-5 Upper molar series (on alveolae) 2r8 Incisive foramen 22'2 Foramen magnum to incisive foramen 69 ! Foramen magnum to palate | 45"8 ' [1893. N. floridana. | Am.M IS. Nat. Hist. No. 1127 No.1129 49-8 1 60 40-5 40 25-2 25 19 19-2 61 7-3 18-5 18-9 27-2 27 20 19-5 9-2 9 10-2 10-5 28-5 27-5 31 29-6 13-8 12-2 62-2 46-9 45-6 22-7 25-1 671 49-4 1893.] NATURAL SCIENCES OF PHILADELPHIA. 19 A NEW EXTINCT SPECIES OF CYPRINID^. By E. D. Cope. Dr. J. Lindalil, Geologist of Illinois, recently sent me some spec- imens of fossil fishes which were found in Pulaski County, in the southern part of that State. They are indifferently preserved on lamina? of a papier kohl of lacustrine origin, which is frequently impregnated with pyrite. Five specimens present characters of value, but no one of them is sufficiently well preserved to furnish all the necessary definitions. However, the specimens agree in all points where comparisons can be made, so that I believe them to pertain to a single species. The characters displayed by this fish refer it to the Cyprinidae, and to the neighborhood of the genus Leuciscus. In specimen No. 8,402 a cast of one of the inferior pharyngeal bones is preserved, and this displacj's three obtusely conical teeth of an external row, and a trace of a single smaller tooth of the internal row. There was apparently another tooth of the external row inferior to and larger than the others ; the four forming a series on a curved line corresponding with the axis of the bone. The ajjices of these teeth are not perfect. The fins do not present any conspicuous spines; and the front of the dorsal fin is above the ventral ; mouth terminal. These characters would refer this fish to Minnilus or Cliola, but another character appears to distinguish it from these. This is the absence of scales. In none of the dozen specimens sent is any trace of scales to be found. As compared with the scaleless genera, the American Meda, and the Old World Aulopyrie, the present fish differs in the absence of conspicuous spines at the front of the dorsal and anal fins. Supposing the absence of scales to be normal, I refer the Illinois species to a new genus under the name of AphelichtJiys. The species I describe as Aphelichthys lindahlii sp. nov. The specific characters are derived from four specimens. These I tabulate as follows: Fin rays. Dorsal Vert. Caudal Vert. D. A. V. C. No. 8,4(i2 1-5 12 11 No. 8,404 -^ 2] 13 No. 8,397 15 , 20 20 PROCEEDINGS OF THE ACADEMY OF [1893. The caudal fin is emargiuate. The general form is moderately slender, much as in our chubs of the genus Semotilus. The length of the head measured above, enters the length to the caudal notch about five times ; and when measured on the side about four times ; and the depth at the front of the dorsal fin enters the same about four times. The mouth is directed obliquely upward, and its rictus appears to be nearly in the line of the anterior border of the orbit. The paired fins are rather short, the pectorals not reaching the ven- trals, nor the ventrals the anal (No. 8,404). The borders of the dorsal and anal are straight (8,402, 8,404). The ribs and vertebral spines are slender. The vertebx-al bodies have on each side a lon- gitudinal median keel, which is bounded above and below by a fossa. Dimensions. MM. Length of superior surface of head of No. 8,402 15"5 Length of No. 8,404a to no|,ch of caudal fin 39*5 Length of head of No. 8,404a on side 9 Total length of No. 8,397 160 Length of head of No. 8,397 on side 41 Length from end of muzzle-to origin of dorsal fin (No. 8,397) 77 The earliest Cyprinidce in North America whose horizon is posi- tively known are from the Idaho beds of Idaho and eastern Oregon, which are of Pliocene age. It is likely that the lake deposit in which the Aphelichthys lindahlii is found is not of an earlier age than the Idaho beds. Species of existing genera of the family occur, however, in the middle Miocene of Eurojie. I dedicate the species to my friend Dr. Josua Lindahl, State Geologist of Illinois. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 21 THE BIRDS OBSERVED IN BRITISH COLUMBIA AND WASHINGTON DURING SPRING AND SUMMER, 1892. . BY SAMUEL N. RHOADS. It is proposed to present in the following pages an ornithologi- cal resume of a collecting trip made in Washington and British Columbia, from March 24 to September 8, 1892, together with an annotated list of the birds observed in those regions. While ornithology claimed the greater part of my time, collec- tions were also made of the mammals, reptiles, shells and plants of the districts visited, concerning which further publications will prob- ably appear in the " Proceedings." The bibliography of Washington and British Columbian ornithol- ogy is very meagre. Since the Cooper-Suckley Pacific Railroad Reports, nothing of much value relating to Washiugton birds has been published except the local lists of Mr. R. N. Lawrence.^ Publications relating especially to British Columbia birds may be included under three titles: " The Naturalist in British Columbia," J. K. Lord, 1866 ; " On a Collection of Birds made by Mr. C. P. Streator in British Columbia," etc., 1890, F. M. Chapman; and "Check List of British Columbia Birds," John Fannin, 1891. Of these the second is authoritative, and based on authentic specimens a remark which in the end equally applies to Mr. Fannin's list, some of his most questionable statements being given on the authority of other persons and his mistakes the evident result of not having con- sulted series of specimens from different localities. Lord's list, given in the appendix to volume second of his work, if judged by the strictest standard of the modern faunal list is nearly worthless in the present connection. It is based on many observations and a few specimens taken on both sides of the forty-ninth parallel, between British Columbia and Washington. On this account I am forced to ignore it. Mr. Chapman's list includes 160 species, while that of Mr. Fannin enumerates 308. To their combined lists I am enabled to add twenty-one species coming under my own observation, seven- teen of which are in the collection. With these additions, the British Columbia list, after throwing out two synonyms (jj^chmophonis I ^ — — lAuk, Jan. and Oct., 1892. 22 PROCEEDINGS OF THE ACADEMY OF [1893. clarkiKJ) and Dendrioca uestiva morcomi) and excluding Drijohates puhescem from Fannin's list, numbers 326. The additional species are : SimorJnjnch ».s puxillus. Charadriws dominieus fulvus. CaUipepla californica vallicola. Buho virf/iiiiaiim. Bubo rin/'nn(i)im subarcticiis. GhtKCuUiiin f/iioma. Perisoreus canadensis capitalis. Chondestes grammacus strigatus. Zonotrichia quenila. Spizella socialis. PassereUa iliaca schidacea. Clivicola ripavia. Vireo huttoni obscurus. Helviinthophila ruficapilla gid- turalis. Dendroica maculosa. Sylvania pusilla. Icteria virens longicauda. Certhia familiaris montana, Parus hudsonicus Columbia nus. Turdus ustulatus suminsonii. Turdus aonalaschkoe pallasii. One of these, Parus Imdsonicus columbianus, is described as new, a detailed notice of which, together with that of ten other species given in this paper, appears in the Auk for January, 1893. To the combined lists of Cooper, Suckley and Lawrence, twenty-five species of Washington birds are added. These, with those not included in Mr. Lawence's Gray's Harbor lists, are: Cohjmbns holb(ellii. Urinator arcticus. Swiorhynchus pusiUus. Synth/iboramphus antiquus. Brachijramph as marmoratiis.'^ Cepphns coliimba.^ Uria troile californica. Lams aryentatiis smithsonianus. La /-UN cu lifornieus.^ Larn.-< delawarensls^ Larus brae hyrhynclms. Phalacrocorax dilophus cincin- atas. Merga nser serrator.^ Lop h odi/tes cucullatus.^ Anas di.'iilil|i;ito. \'ery jibuiulant on PaciHc* Coast ami Paget Sound in spring. Hivedinu' in the iiitoi-ioi- lako districts. Aslioroft, Clinton, T>ac La Iladu'. 34. Anas oarolineiisis. (iici'n-wiiif; 'I'oal. Assonihlini:- in inoredible numbers on the Hats of Nisqually River. Kosortiuii- with others to the interior in summer. 35. Anas discors. I'luc wins; Teal. Mr. Fannin calls this a " very rare bird " in British Columbia. I found it breeding about several of the small lakes in the vicinity of Tjac La Hache. A nuile, female and three young were secured. 36. Anas cyauopteia. ('imiiimoii 'I'omI. To Mr. I'^annin's two records of this species I can add several. Ill the smaller, more retired, woodlaml lakes along the Cariboo Road above Clinton, I frequently Unshed the Cinnamon Teal. Only one specimen was secured. ^Ir. I). ^LcKinley, Lac La Hache, says the " red teal " breeds sparingly in that neighborhood every year. 37. Spatula clypeata. Shoveller. Numerous on Puget Sound in s|)ring. A few found breeding along the Cariboo Road. 38. Dafila acuta, rintail. Abundant in all coast waters during migrations; breeding throughout the interior. *39. Aix sponsa. Woinl IMu-K. Karely met with. Pugel Simnd specimens in Ivlwards Pros, museum. 40. Aythya americana. lUvI lu-ml. Reported as a rare duck in the vicinity of Tacoma, by Edwards Bros. A few were found breeding with .1. ralli!uck. Rare in Puget Sound, P^dwards 15ros. Rare at Lac La Hache, Duncan McKinley. 49. Oidemia amerioaua. American Scoter. A few noted at Nisqually among flocks of 0. deglandi. *.50. Oidemia deglandi. White-winged Scoter. j\[ost abundant of the genus, both on the coast and mainland interior. I am convinced it breeds as far south as 150-Mile House, Cariboo Road, individuals being .seen at Lac I>a Hache July 4. *51. Oidemia perspicillata. Surf Scoter. Fairly abundant on coast sounds and harbors during my stay. "'52. Erismatura rubida. Kuddy Duck. Sparingly represented on the interior lakes during sunnner. Not met with on coast. Puget Sound, I{!dwards Bros. ■••53. Anser albifrons gambeli. American White-fronte Zoe, Dec, 1890, p. 307. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 55 224. Dendroica townsendi. Townsend's Warbler. Rare east of Cascades, but abundant in Washington and on Van- couver Island. 225. Seiuras noveboracensis notabilis. Grinnel's AVater Thrush. Found breeding along interior streams. Lac La Hache and Bonaparte. 226. Geothlypis macgillivrayi. Macgillivray's Warbler. Found breeding at all localities and elevations. 227. Geothlypis trichas occidentalis. Western Yellow-throat. Rare on Vancouver Island. Abundant at Lulu Island and about the shores of reedy lakes in the interior of British Columbia. 228. Icteria virens longicauda. Long-tailed Chat. In the bushes which line the banks of the Thompson River below Ashcroft I secured two males of this species. Another was heard singing on a ranch above the town. Fort Lapwai, Idaho, was here- tofore the most northern record for this Chat. 229. Sylvania pusilla. Wilson's AVarbler. Sylvania pusilla pileolata. Pileolated Warbler. The series of Wilson's Warblers taken in eastern and western British Columbia, compared among themselves and with specimens from the Atlantic States, are devoid of any differences which would justify their separation. There is a singular uniformity in the aver- age measurements of specimens from all localities and, saving two specimens from Vancouver Island which show deeper yellow on the forehead, their coloration is remarkably uniform. Judged by the specimens examined, there is not, when we consider its transconti- nental range, a more "hard and fast" species than Sylvania pusilla. North of the United States S. pusilla pileolata has no better claim to recognition than Dendroica aestiva morcomi. 230. Setophaga ruticilla. Redstart. Well represented all over interior British Columbia. 231. Anthus pensilvanicus. American Pipit. Washington and the Province of British Columbia at large. Breeding sparsely on the plateaus and' mesas of the interior, up to 4,000 feet. 232. Cinclus mexicanus. American Dipper. Associated with all dashing streams, from the mountains to the sea. 56 PROCEEDINGS OF THE ACADEMY OF [1893. 233. Galeoscoptes carolinensis. Cat Bird. Not abundant anywhere and very local in its distribution. It does not appear to get farther north than Clinton. The brownish cast of upper parts, especially on the crown, rarely seen in eastern skins, is very marked in some British Columbia examples and is present in nearly all of them. Western birds average darker beneath than specimens from the Atlantic coast. Measurements of thirteen specimens (including the Streator series) from British Col- umbia, give the following averages as compared with those of a series of ten from the eastern United States. Wing. Tail. Exposed Culmen. Tarsus. British Columbia 2-58 3-78 -62 MO Atlantic States 3-54 3-75 '63 1-12 Both of these differences and those of coloration are too slight and variable to warrant any subdivision of the species. ■234. Salpinctes obsoletus. Rock Wren. Found about Ashcroft and northward to Cache Creek; also at Kamloops where one was nesting in a " section house," ten feet from the railroad tracks. Five specimens from Ashcroft do not materially differ from Arizona and Utah skins. 235. Thryothorus bewickii spilurus-. Vigor's Wren. Abundant in the west Cascade region of Washington and Brit- ish Columbia. It is doubtful whether this species ever crosses the coast mountains to the interior, it being essentially a lover of lower levels. 236. Troglodytes aedon parkmanii. Parkman's Wren. I never found Farkman's Wren above the 2,000-foot limit. It is not as abundant or evenly distributed in the interior as coastwise. 237. Troglodytes hiemalis pacificus. Western Winter Wren. Abounding on the coast. Two moulting birds from the Selkirk Mountains near Nelson are even darker than skins from Puget Sound. I did not find any Winter Wrens in the arid interior of British Columbia west of the Gold Range, nor at Lac La Hache. The reappearance in the Selkirks of typical pacificus and its absence again from the Rockies at Field tallies perfectly with the alterna- ting climatic conditions already pointed out as occurring across this vast area. Dr. jNIerriam calls the Winter Wren foimd by him in the Saw Tooth Mountains, Idaho, hiemalis. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 57 238. Cistothoms palustris paludicola. Tule Wren. Breeding over the lake country east of Cascades. I found it abundant at Lac La Hache. It must range much farther north than this, probably (G. Hamilton) to Stewart's Lake, British Col- umbia, latitude 54°. 239. Certhia familiaris montana. Kocky Mountain Creeper. Rare in British Columbia. A male Creeper from Nelson appears to be montana. 240. Certhia familiaris occidentalis. California Creeper. Neither rare nor common on the Pacific slope. Rare at Nis- qually. Probably reappears on interior mountain peaks. 241. Sitta carolinensis aculeata. Slender-billed Nuthatch. One specimen was taken at Tacoma. It is rare on the coast but abounds in the wooded hills of the interior of British Columbia. 242. Sitta canadensis. Red-bellied Nuthatch. East and West of Cascades ; also in the Rocky Mountains. 243. Sitta pygmaea. Pygmy Nuthatch. Only found, and that sparingly, at Vernon. 244. Par us atricapillus septentrionalis. Long-tailed Chickadee. Abound in the inter-mountainous region of British Columbia, up to 3,000 feet. 245. Paras atricapillus occidentalis. Oregon Chickadee. Abound in the coast region. 246. Parus gambeli. Mountain Chickadee. Found in the interior mountains of British Columbia but not in the Rockies. 247. Parus hudsonicus columbianus, subsp. nov. Columbian Chickadee. Four specimens of this strongly differentiated ally of hudsonicus were secured in the high mountains surrounding Field, British Col- umbia. They were abundant in the deepest and darkest recesses of the coniferous forest, associating in flocks of ten to twenty individ- uals after the familiar manner of the genus. A description of this new form having already appeared in the Auk, it is useless to refer to it further here except to say that it is larger and darker than hudsonicus, with a much larger bill and with the throat patch jet black instead of brownish-black. 5 58 PKOCEEDINGS OF THE ACADEMY OF [1893. 248. Parus rufescens. Ch«stnut-backed Chickadee. Very couimoa ou the coast aud Islands but never found east of the Cascades. 249. Begulas satrapa olivaoeas. Western Golden-crown«d Kinglet. I can tiud uo color diHereuce between the east and west Cascade Kinglets. In this respect they agree with the British Columbia "Winter Wrens, 250. Eegulus calendula. Ruby -crowned Kinglet. Numerous ou the coast in spring. Breeding in the interior. The nuptial song of this tiny bird is a truly marvellous production. Perched in the top of a giant tir it will remain motionless for thirty minutes at a stretch, singing an incessant hurly-burly loud enough to be heard half a mile away. 251. Mjadestes townsendii. Townsend's Solitaire. I secured a Solitaire on Vancouver Island in May. They were met with at high altitudes on both slopes of the Cascades, Selkirks and Rockies, as far north as the 52nd parallel, increasing in abun- dance eastward ly. 252. Turdus fasoesens salicicolas. Willow Thrush. In all visited localities of the interior. Breeding at Lac La Hache. This extends Mr. Streator's nesting record of the species 150 miles farther north. 253. Ttirdas ustulatus. Russet-back Thrash. Abundant coastwise. 254. Turdus ustulatus swainsonii. Swainson'is Thrush. A female and young male in nesting plumage shot at Nelson where they were tairly abundant. 255. Turdus aonalaschkae. Dwarf Hermit Thrush. On the coast in migrations. Probably breed in the Cascades and mountains of Vancouver Island. I was surprised to again meet this species at Field, where I saw many aud secured three birds. One of these in spotted nesting plumage proves that the summer habitat of the Dwarf Thrush is far more extended than formerly supposed and accounts for the appearance of this form in Utah aud Nevada in fall migrations. 256. Turdus aonalaschkae pallasii. llermit Thrush. That j)allasii aud not auduboni breed in the region around Lac La Hache is attested by certain skins in the collection. Neither 1893.] NATURAL SCIENCES OF PHILADELPHIA. 59 form wa3 found iu any other part of British Columbia, If it be found that aonalaschkce and paUasii breed indifferently across com- mon ground in the interior and Rocky Mountain regions of British •Columbia, without the intervention of intermediates, a more com- plete separation of the two than is now recognized must be made. At least two points are established by skins in the collection — 1st the breeding of aotudaschkae in the Rocky Mountains of British ■Columbia ; 2nd, the breeding of pallasii west of the Rockies and south of the 52nd parallel. 257. Merulamigratoria propinqua. Weeteru Robin. Uniformly abundant everywhere. 258. Hesperooichla naevia. Varied Thrush. Abundant on the coast, but by no means confined thereto, being found at high altitudes on all the mountains of the interior to the Rocky Mountain summits. 259. Sialia mexicana. AVestern Bluebird. Not common anywhere but less so in the east Cascade districts where it does not range beyond the Transition Zone. 260. Sialia arotica. Arctic Bluebird. Abundant in northern and western interior portions of British Columbia. A tabulated list of all the specimens forming the author's collec- tion of British Columbia and Washington birds, including those collected by Messrs Morris and Evans in the same region, is appen- ded. The collection has been recently purchased by the Academy of Natural Sciences. 60 PROCEEDINGS OF THE ACADEMY OF [1893. m u 0 P3 tT L) CJ a. U c oi o ^ B o a hJ 1 O c 0 ^ (4 ^ Colymbus auritus Podilymbus podiceps Urinator imber Urinator arcticus Synthliboramphus antiquus Brachyramphus marmoratus Lams glaucescens Larus occidentalis Larus californicus Larus delawarensis Larus brachyrhynchus Larus Philadelphia Merganser americanus Merganser serrator Anas boschas Anas americana Anas carolinensis Anas discors Anas cyanoptera Spatula clypeata Dafila acuta Aythya vallisneria Glaucionetta clangula americana Glaucionetta islandica Charitonetta albeola Oidemia deglandi Branta canadensis Branta canadensis hutchinsii Branta canadensis occidentalis Ardea herodias Forzana Carolina 1893.] NATURAL SCIENCES OF PHILADELPHIA. 61 .c u d ►2 n pq ^ (J (j u « cJ 0 s s 4J ■3 1— 1 la i 0 u pq "in 0 •a 2 0 pg J" 1 d c 0 a. 0 0 1 pq 3 0 s 0 0 u pq a 0 pq cuo a JS s c u CS w^ s rt "3 in 0 •■^ ns c« 0 J < CQ U h-l i4 W > ^ £ Crymophilus fulicarius 1 Tringa minutilla 1 Tringa alpina pacifica 3 2 Ereunetes occidentalis 3 8 Totanus melanoleucus 1 2 1 Actitis macularia 1 3 Numenius longirostris 1 1 ■Charadrius dominicus fulvus(?) 1 Aegialitis vocifera 3 •Callipepla californica 1 2 ■Callipepla californica vallicola 1 Dendragapus obscurus fuligi- nosus 2 5 JDendragapus obscurus richard- sonii 1 2 Dendragapus franklinii 1 iBonasa umbellus togata 2 2 4 Bonasa umbellus sabini 3 1 Pediocaetes phasianellus colum- bianus 3 1 Columba fasciata 2 Zenaidura macroura 1 2 •Circus hudsonicus 1 1 1 Accipiter velox 1 1 1 1 Accipiter cooperi 2 Buteo swainsoni 3 Falco columbarius 2 Falco columbarius suckleyi 1 Falco richardsonii 1 Falco sparverius 7 1 2 2 I 2 • Asio accipitrinus 1 Symium occidentale 2 Nyctala acadica 1 Megascops asio kennicottii 1 62 PROCEEDINGS OF THE ACADEMY OP [1893. u pa 'ji 0 u i-i m P9 1) o 1— 1 o u u B ^ pa > ihJ i ^; u. Bubo virginianus Bubo virginianus subarcticus Bubo virginianus saturatus Glaucidium gnoma Glaucidium gnoma californicum Ceryle alcyon Dryobates villosus leucomelas Dryobates villosus harrisii Dryobates pubescens gairdneri Dryobates pubescens oreoecus Sphyrapicus varius nuchalis Sphjrapicus ruber Ceophlocus pileatus Melanerpes torquatus Colaptes cafer Colaptes cafer saturatior Chordeiles virginianus Cypseloides niger Trochilus rufus Tyrannus tyrannus Tyrannus verticalis Sayornis saya Contopus borealis Contopus richardsonii Empidonax difficilis Empidonax pusillus Empidonax pusillus traillii Empidonax hammondi Otocoris alpe&tris merrilli Pica pica hudsonica Cyanocitta stelleri 11 12 11 1893.] NATURAL SCIENCES OF PHILADELPHIA. 65 ^ (J u J* m m •V a "m (J U U § V > a o o a 1— 1 3 2 o C9 c o a o ifl 3 O a 05 3 O '^ ti CU > J < M U U t4 OJ Cyanocitta stelleri annectens Perisoreus canadensis capitalis Perisoreus obscurus Gsrvus corax sinuatus Corvus americanus caurinus Picicorvus columbianus Molothrus ater Agelaius phoeniceus Sturnella magna neglecta Icterus bullockii Scolecophagus cyanocephalus Pinicola enucleator Carpodacus purpureas califomi- cus Loxia curvirostra minor Acanthis ? Spinus pinus Poocaetes gramineus Ammodramus sandwichensis Ammodramus sandwichensis al- audinus 2^notrichia leucophrys interme- dia Zonotrichia leucophrys gambeli Zonotrichia coronata Spizella socialis Spizella socialis arizonae Spizella breweri Junco hiemalis oregonus Junco hiemalis shufeldtii ? Melospiza fasciata guttata Melospiza lincolni Passerella iliaca unalaschensis 1 1 1 1 8 3 2 1 2 2 6 6 3 3 3 2 3 5 1 1 1 8 11 2 1 1 8 4 6 1 3 2 1 5 12 2 6 2 3 5 4 5 17 8 2 3 1 4 12 4 2 1 3 3 U 5 1 1 6 3 1 1 64 PROCEEDINGS OF THE ACADEMY OF [1893. U n 0 u u u U M n c 12; 2 Passerella iliaca schistacea Piplio maculatus megalonyx Pipilo maculatus oregonus Habia melanocephala Passerina amoena Piranga ludoviciana Progne ? Petrochelidon lunifrons Chelidon erythrogaster Tachycineta bicolor Tachycineta thalassina Clivicola riparia Stelgidopteryx serripennis Ampelis cedrorum Lanius borealis Vireo olivaceus Vireo gilvus swainsonii Vireo solitarius cassinii Vireo huttoni ( obscurus) Helminthophila ruficapilla gut turalis Helminthophila celata Helminthophila celata lutescens Dendroica aestiva Dendroica coronata Dendroica auduboni Dendroica maculosa Dendroica townsendii Seiurus noveboracensis notabilis Geothlypis macgillivrayi Geothlypis trichas occidentalis Icteria virens longicauda 1893.] NATURAL SCIENCES OF PHILADELPHIA. 65 JS o cJ f i 3 o w 'v CJQ . 3 : Oh 'in \ 1—1 4) % \ 8 c > 0 3 :3 2 o ! JS ! < 1 PQ i- s o CQ oq 1 0 V U o o en 3 O i u M c o □ > u pg c o J2 V 0 ^ylvania pusilla 8 1 1 1 Selophaga ruticilla Anthus pensilvanicus 8 1 Cinclus mexicana 6 •Galoescoptes carolinensis 2 5 1 Thryothorus bewicki spilurus 4 1 1 Troglodytes aedon parkmani 3 4 1 Troglodytes hiemalis pacificus 3 3 2 Cistothorus palustris paludicola 2 7 Certhia familiaris montana 1 Certhia familiaris occidentalis 3 Sitta carolinensis aculeata 1 2 2 Sitta canadensis 4 Sitta pygmaea 3 Parus atricapillus septentrionalis 1 1 1 1 1 Parus atricapillus occidentalis 8 5 Parus gambeli 2 2 1 3 Parus hudsonicus columbianus 4 Parus rufescens 10 6 Regulus satrapa olivaceus 4 6 1 1 2 2 Regulus calendulus 2 1 Myadestes townsendi J 1 Turdus fuscescens salicicolus 1 1 2 2 Turdus ustulatus 9 2 Turdus ustulatus swainsonii 2 Turdus aonalaschkse 3 Turdus aonalaschkse pallasii 2 Manila migratoria propinqua 4 5 2 1 1 3 1 Hesperocichla naevia 9 4 1 Sialia mexicana 2 2 Sialia arctica 1 1 1 5 66 PROCEEDINGS OF THE ACADEMY OF [1893. February 7. The President, General Isaac J. Wistae, in the chair. Fifty-nine persons present. The deaths of the following members were announced : — John Markoe, February 1, 1893 ; F. A. Genth, M. D., February 2, 1893. Papers under the following titles were presented for publication: — " Notes on some Minerals and Rocks," by Edw. Goldsmith. " A Contribution to the Herpetology of British Columbia," by Edw. D. Cope. " Pyrophyllite Slate in Northern Pennsylvania," by Abraham Meyer. " Notes on the Occurrence of Quartz and other Minerals in the Chemung Measures near the Line of Wyoming and Tioga Counties," by Abraham Meyer. February 14. The President, General Isaac J. Wistar, in the chair. Forty-two persons present. The death of Joseph C. Turnpenny, a member, July, 1892, was announced. February 21. The President, General Isaac J. Wistar, in the chair. Forty-seven persons present. A paper entitled " Involution Form of the Tubercle Bacillus and the Effect of Subcutaneous Injection of Organic Substances on Inflammations," by S. G. Dixon, M. D., was presented for publication. February 28. The President, General Isaac J. Wistar, in the chair. Twenty-eight persons present. The death on the 26th inst of Mr. Jacob Binder, Curator of the William S. Vaux Collections, was announced, whereupon the follow- ing minute was adopted : — 1893.] NATURAL SCIENCES OF PHILADELPHIA. 6T The Academy having heard with sincere regret of the death, the 26th inst., of Mr. Jacob Binder, the Curator of the William S. Vaux Collections, it is fitting that a record be made of the society's- appreciation of the loss which it has thereby sustained. During the latter years of Mr. Binder's life, from his election to- membership in January 1879 until incapacitated by the lingering illness which has just terminated fatally, his best energies have been devoted to farthering the interests of the Academy. He performed his duties as Curator from January 1883 tO' January 1892, as member of the Board of Trustees of the Build- ing Fund from January 1884 to February 1890 and as Curator of the William S. Vaux Collections since 1883, with energy, discretion and liberality. His knowledge of business details was of the utmost value in the financial administration of the society, while his^ personal qualities were such as to endear him to his associates. The Academy desires to convey to Mr. Binder's wife and children? the assurance of its profound sympathy in their bereavement. On the recommendation of the Council the following were elected to constitute the Committee on the Hayden Memorial Geological Award : — Angelo Heilpriu, J. P. Lesley, Persifor Frazer, Benjamin Smith Lyman and William B. Scott. The Council reported the election of Benjamin Sharp, M. D., to fill the vacancy in the Committee on Instruction and Lecturer caused by the death of Mr. Isaac C. Martindale. The following were elected members : — Joseph Sailor, M. D., Henry Erben, Warner J. Banes, Walter Erben, Charles M. Thomas, M. D., Harold H. Kynett, M. D., Ernest La Place, M. D., Edw. C. Kirk, M. D., Henry L. Taggart,, William B. Scott and H. Frank Moore. The following were elected correspondents : — The Rt. Hon. Lord Kelvin, Leonard Stejneger of Washington, D. C, Charles B. Cory of Boston, Mass., Arnold Lang of Jena, Germany, Robert Ridgway of New York, William Brewster of Boston, Mass. and J. A. Allen of Cambridge, Mass. The following were ordered to be printed : — 68 PROCEEDINGS OF THE ACADEMY OF [1893. THE INTERPRETATION OF CERTAIN VERSES OF THE FIRST CHAPTER OF GENESIS IN THE LIGHT OF PALEONTOLOGY. BY HENRY C. CHAPMAN, M. D. To those unfamiliar with the fact that the text of Genesis has Ijefore now constituted a subject of discussion before the Academy,^ some apology on the part of the author might be thought appropri- ate for the introduction of such a subject for its consideration. It might naturally be supposed also that there could be but little left to say as to the interpretation of the first chapter of Genesis in the light of paleontological research, especially in view of the consid- eration recently given to that subject by such distinguished contro- versialists as Mr. Gladstone^ and Prof. Huxley.^ As the latter dis- cussion, as well as many other similar ones, appears to have been based almost entirely upon the text of the English version of the Old Testament, revised or otherwise, it may not be regarded as superfluous if the order of the creation of life as given in the original Hebrew and literally translated, be compared with the order in which life appeared according to the testimony of the rocks. To those having no knowledge of Hebrew it should be mentioned that the language is an exceedingly elastic one, especially in the hands of those skilled in Hebrew exegesis — the same word having undoubtedly very many different meanings, according to the context, etc. By far the greater number of the stem words in Hebrew consist of three consonants and the system of " pointing," or the vocalization of such stem words by the addition of points, was introduced by the Jews with the view of fixing definitely the mean- ing of the stem words. Thus, for example, the word CIS Adm, read in Hebrew from right to left, will mean either " he was red," ^' red," or " man," according as DIJ^ is written with the points, as DlX, DIX, DIK. The system of pointing or the vocalization of the stem words was, however, only introduced in comparatively recent times (in the interval between the composition of the Targum from the third to the sixth centuries and the making of gram- mars by the Jews in the Arabic language in the beginning of the tenth century) and therefore long after the original Manuscript 1 Proc. Acad. Nat. Sciences, 1854. 2 Nineteenth Century, 188.5, 1886. ^ Nineteenth Century, 188 ), 1886 — Essays upon some Controverted Questions, 1892. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 69^ Bibles were written. The Hebrew Bible used to-day by students is usually that in which the words are " pointed," the translation of such words as given in the Hebrew- English Dictionary being that determined upon by Jews living about 1,200 years ago. No doubt such Jews, in the pointing of stem words, as well as the translators of the Bible into English in modern times, were influenced by the interpretation of the Hebrew as given in the Greek translation made by the Seventy at Alexandria in the reign of Ptolemy Philadelphus, and by Aquila, Theodotion and Symmachus, and in the Latin Vulgate of St. Jerome, all six of which versions, it may be mentioned, were incorporated by Origen in his famous Hexapla Bible. The authority, therefore, for the accepted pointed Hebrew text and for the old and revised versions of the English Bible is weighty indeed. It is with great diffidence, therefore, that the author presumes to offer any other interpretation than that usually accepted of those verses in the first chapter of Genesis relating to the creation of animal life. The account of the creation of animal life as given in the first chapter of Genesis begins with the 20th Verse, which we give in the original unpointed Hebrew, together with a literal translation of the same : n^n tys] Y^'Z* c^d- i^-id*^ d'^-^s* n!2«^i living creature reptile waters the abundantly produce shall Aleim said and but which, according to the English version, old or revised, is trans- lated, " And God said let the waters bring forth abundantly the moving creature that hath life." heavens the of expanse the of faces the above earth the above flutter shall birds rendered according to the authorized version, " and fowl that may fly above the earth in the open firmament of heaven." Admit- ting that, while our translation of the Hebrew' is far less beautiful and elegant than the language of the old or revised version, it is nevertheless correct, it will be observed that the Hebrew word j*"itt^, shrtz, is translated by us "reptile" instead of "moving creature," and Diy, ouph, "bird "instead of "fowl." The translation of the word shrtz " reptile " instead of " moving creature " or " creeping creature " as given in the marginal reading of the English versions is justified first by its etymology, it being derived from the verb shrtz, " to creep or crawl or to produce abundantly," and second, from the fact of it being translated by the Seventy, Aquila and Theodotion tp-sra^ 70 PROCEEDINGS OF THE ACADEMY OF [1893. by Syramachus tp-sr6v, and by St. Jerome in the Vulgate, reptile. Now while it may be urged by those who favor the text of the English versions that as a reptile is a moving or creeping creature the word shrtz may be so translated it does not necessarily follow that all moving creatures are reptiles. It is obvious, therefore, that if the order of creation according to Genesis is to be compared at all with the order of evolution according to the testimony of the ^ocks, precise rather than general interpretations, as far as possible, must be offered of the Hebrew words in question. The Hebrew ■word ouph, derived from the stem word meaning to vibrate, to flutter, 40 fly, we have translated "birds" rather than "fowl," as there is nothing in the context to indicate that fowl especially were the first birds created. According then to the 20th verse of the first chapter ■of Genesis reptiles were created first and birds of some kind afterward. It is admitted by paleontologists that the earliest formations in which the remains of reptiles have been found are of Permian age, the remains found in the earlier carboniferous strata being rather Amphibian than Reptilian in character. It is also admitted that the earliest formations in which the remains of birds have been found are of Jurassic age, a much later formation than the Per- mian. According to the testimony of the rocks, then, reptiles appeared first and birds of some kind afterward, and this is true •even if the supposed footprints found in Triassic rocks should have been made by bird-like animals, since the Triassic as well as the Jurassic formations are of later date than the Permian. Such Iseing the case, the sequence of life as given in the 20th verse of Genesis is the same sequence as that of the rocks. Continuing now the exposition in the 21st verse, according to the original Hebrew, living creature every the and great reptiles the Aleim created and wing of bird every the and kind their for waters the abundantly produced which moving ■or according to the old and new versions " And God created great whales (0. V.), the great sea-monsters (N. V.), and every living creature that moveth which the waters brought forth abundantly .after their kind and every winged fowl. " The only two words in the above verse the interpretation of which ■demands especial consideration are tninm and rmsh. The word tuinm is translated in the Vulgate cete, and in the old English ver- sion " whales," in the Septuagint jf^yVij, and in the new version " sea- 1893.] NATURAL SCIENCES OF PHILADELPHIA. 71 monster," the word used in the old English version being apparently based upon the Latin, that in the new upon the Greek translations of the Hebrew Bible. The word tninm is derived, according to some Hebrew grammarians from tne, to shriek or wail, and denotes in the form of a noun some kind of serpent, on account of the hiss- ing noise made by such animals. By others, however, the root is supposed to be tnn, to extend, the noun derived from the latter indicating an elongated kind of reptile, such as a great serpent or sea monster of some kind. That the word tninm, however derived, refers to some kind of reptile is shown by it being rendered in the 148th Psalm, 7 verse, in the Septuagint, dpaxwrs?, in the Vulgate dracones, and in the English versions " dragons." While the word tninm might be translated " sea monsters," since reptiles like the Dinosauria, etc., are regarded as sea dragons in a popular sense, it is •difficult to justify the rendering of the word by " whales." Further, if the latter interpretation of the word be accepted the difficulty will then present itself of reconciling the statement of Genesis that whales were created before mammals with the evidence of the rocks that goes far to prove that the whales have descended from carnivorous mammals like the seals, the Zieuglodon, an extinct cetacean form combining in many respects the characters of both these orders. On the supposition, however, that by tninm is meant rep- tiles of some kind there is no difficulty in reconciling the statements in Genesis with the facts of paleontology, the reptiles (schrtz) appearing in Permian and Triassic times, such as Proterosaurus, Nothosaurus, Khynchosaurus, etc., being followed by very different kinds of reptiles (tninm) in Jurassic and Cretaceous eras. Marine monsters like the Plesiosaurus, Ichthyosaurus, Elasmosaurus, Edestosaurus and land monsters of which Hadrosaurus, Lselaps, Iguanodon and Megalosaurus are examples. The Hebrew word rmsht being derived from the stem word rmsh, to move, is rendered both in the old and in the revised versions by " moveth," and in the Vulgate by " motabilem." As rmsh secondarily, how- ever, means to creep or to crawl it was translated by the Seventy kpiteroiv. All aquatic animals that moveth, creepeth or crawleth are not, however, necessarily reptiles since there are mammals that " moveth " in the water and " creepeth " or " crawleth " out of it. Indeed, in the reference made in Gen., c. 7 : v. 21, to the death of all flesh " that moveth upon the earth, both of fowl and of cattle and of beast," and in Psalm 104, v. 21, " wherein all of the beasts 72 PROCEEDINGS OF THE ACADEMY OF [1893. of the forest do creep," the word used in the original Hebrew to express the idea of beasts moving or creeping is rmsh. The word rrash being so associated with beasts it is as justifiable to suppose that the moving or crawling animals that the waters so abundantly pro- duced at this period of the earth's history, "day the fifth " so-called, were aquatic mammals as that they were aquatic reptiles. Such an interpretation is consistent with the facts of paleontology, the earliest mammal yet discovered, Dromatherium, obtained from rocks of Triassic age and probably of monotrematous nature, being preceded by reptile-like animals, such as the theromorphric Pelycosauria of the Permian, described by Cope. Returning to the exposition of the 21st verse it will be observed that while in the 20th verse, in referring to the creation of birds, the Hebrew word ouph alone is used, in the 21st verse the same word is coupled with another word, kup. The word knp, being derived from the stem word knp, to cover, when used as a S ^ y a a un noun should be translated " wing," the Arabic word v_fl,X> ^°f having that meaning. The birds with wings, ouph, knp, were created then, according to Genesis, after the birds ouph, presumably without wings. The order of creation, however, is that of evolu- tion, since the reptiles appeared first, being followed by reptile-like birds, Compsognathus, and bird-like reptiles, Archeopteryx, Hes- perornis (Marsh.) Passing now to the consideration of the 24th verse, containing the account of the creation of beasts, and translating the original Hebrew literally we would read as follows : nrj:^ -•'n a^'s: '^-^'^Tx s:tin d^-^« nos"''! kind its for living creature the earth the forth bring shall Aleim said and p« in^m tt'ani -Dna earth the of beasts wild and thing moving and cattle or as rendered in the old and new Versions " And God said let the earth bring forth the living creature after his kind, cattle and creep- ing thing and beast of the earth." The HebrcAV word bhm is probably derived from a stem word, bhm, though as a matter of fact there is no such verb in use at the present day. As the kindred words in the Arabic and the Ethio- pmn languages signify, however, "dumbness," the word used in Hebrew as a noun has come to be accepted as meaning "dumb beasts." According to this interpretation it was rendered by the Seventy,. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 73 T£zpd7:oda, four footed and in the Vulgate, Jumenta, draught cattle. The word rmsh we have translated " moving thing," consistently with the interpretation already given of that word in verse 21. The word was translated ifj-sra iu the Septuagint and reptilia in the Vulgate ; inconsistently in the latter case, however, as essentially the same Avord was previously rendered motabilem. It is difficult to understand why the word " reptile" should be associa- ted with cattle and wild beasts as the context would lead one to suppose that at this late period in the creation of animal life beasts were more particularly created. It is immaterial, however, to the argument whether rmsh be translated in this verse "reptiles" or " moving, creeping or crawling creatures," since it is not to be sup- posed that reptiles at once ceased to appear upon the earth. The translation of the Hebrew word hitu admits of no discussion, being translated in the Septuagint 'fr^pta, in the Vulgate bestias and in the English versions " beasts." It will be remembered that the first mammalia appearing upon the earth, the descendants of reptiles, were probably INIonotremata, resembling the Ornithorynchus and Echidna of the present day. From such lowly organized mamma- lian forms descended the mammalia of the early Tertiary which in turn gave place to the mammalia of the later Tertiary and present geologic epochs. As the " beasts," " mammalia," the bhm of the Hebrews were created on "day the sixth," that is after the rmsh or promammalia, the account of the creation of the mammalia as given in Genesis is therefore consistent with the order of the evolution of the mammalia as based upon the testimony of the rocks. Resuming what Genesis states as to the creation of life, it appears, if the trans- lation just submitted be accepted as correct, that during "day the fifth " the ancestors of the reptiles, the proreptilia, appeared upon the earth, being succeeded during that period successively by the ances- tors of the birds, the pro-aves, reptiles, the pro-mammalia and birds, and that during the following period, " day the sixth," the mammalia appeared. The accompanying diagram will illustrate succintly and genealogically the oi'der of creation as just given. The order of creation then, as given in the verses of the first chapter of Genesis just translated, is essentially the same order as that based upon the remains of animal life preserved in the rocks. It may be argued, however, that the account of the creation of ani- mal life as given in Genesis is very meagre, nothing being said as to the creation or appearance of the lower forms of life, fishes even being 6 74 PROCEEDINGS OF THE ACADEMY OF [1893. only incidentally alluded to in verses 26 and 28 as among the ani- mals given to man to rule over. The prescribed limits of this essay Mammalia bhm Aves ouph knp Pro-mammalia rmsh Reptilia tninm Pro-aves ouph Pro-reptilia shrtz do not permit of the consideration of such meagreness, its object being simply to show that the order of creation according to the first chapter of Genesis so far as it is given, is consistent with the well established facts of paleontology. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 75 THE INHERITANCE OF MODIFICATIONS DUE TO DISTURBANCES OF THE EARLY STAGES OF DEVELOPMENT, ESPECIALLY IN THE JAPANESE DOMESTICATED RACES OF GOLD-CARP. BY JOHN A. RYDER. The recent experiments in shaking apart the cells produced by the first cleavage in the eggs of Echinoderms by Driesch, and of Amphioxiis by Wilson, as well as the experiments of Roux, in the same direction, with frogs' egga, show that it is possible for a single one of the two blastomeres resulting from the first segmentation to produce at once a complete embryo, or at any rate to finally recon- stitute the missing half by means of what Roux has called post- generation as in the case of the frogs' eggs. These experiments, leading to the development of two separate embryos from the same single egg, have been regarded as so remark- able that they have caused a good deal of discussion. They are, however, it seems to me, to be regarded as having much in common with phenomena that at first thought seem to be widely distinct from them, namely, the production of monstrosities in invertebrates and vertebrates. The occasional duplication of peripheral parts also, such as the tail in lizards when broken off", and an excess of toes or fin-rays, perhaps, may be regarded as belonging ulti- mately to the same category of phenomena, with a similar set of causes operating to produce them, namely, profound disturbances of the normal processes of karyokinesis during development or at the moment of the beginning of the regeneration of lost parts. Weber's experiment, reported many years ago, proving that the eggs of the common pike, Emx lucius, could be caused to produce double monstrosities if the recently fertilized ova were violently shaken, is well known. The experience of fish-culturists in hand- ling the eggs of Salmonoids is also well known. A man of very great experience in the fish-cultural establishments of Austro- Hungary informed me some years since that so great was the danger in roughly handling or shaking the ova of the Salmonoids, during the very early stages of their development, that carelessness in this respect would result in producing monstrosities almost exclusively. I have myself, while employed as an assistant by the U. S. Fish Com- mission, seen batches of salmon brood, which were almost entirely composed of fry that had developed as double or triple monsters, «ach with but a single yolk. 76 PROCEEDINGS OF THE ACADEMY OF [1893. The well-known experiments of Dare^te in artificially producing monstrosities during the incubation of bird's eggs, are also well known, as well as his methods of experiment, which consisted in shaking the eggs, varnishing a portion of the shell or placing them in an abnormal position, upon one end, for example, during the early days of incubation. Similar experiments have also been made by others, that abundantly confirm the conclusion that abnormal conditions or absolute mechanical disturbances during segmentation are the causes of such duplication of the embryo. Rauber attacked the problem from a morphological standpoint and indicated in some measure the method according to which the doubling occurred in the germinal disk of the eggs of fishes, working upon the blasto- derm of the eggs of the Pike, Esox. He showed that the embry- onic axis was duplicated or triplicated, as the case might be, at the border of the blastoderm. That the distance apart of the two con- temporaneously developed embryos along the rim of the blastoderm, determined the degree to which their axes would be ultimately fused or distinct when the larval development had been completed. In the study of a series of double monsters of the common lobster, Homarus Americamcs, I found that some similar law applied in some way, but unfortunately the very early stages were not seen, so that it could not be formulated with precision. The evidence for the existence of such a law was, however, sufficiently complete to war- rant certain general deductions, since various degrees of fusion were seen which were perfectly parallel to those of fishes, except that instead of the ventral aspects being fused where the rudiments of the embryo had been first formed at 180° apart on the blastoderm,, it was here the dorsal aspects that were fused, a fact which is as strictly in conformity with the morphology of the Arthropod series, to which the lobster belongs, as the fusion of the ventral aspect of the embryo of vertebrates is in conformity with the morphology of the adult vertebrate body. The discovery of Kleinenberg that the embryos of certain earth- worms studied by him, were sometimes double and coherent, shows that such a method of double development is widely distributed within the series of Bilateralia or bilaterally symmetrical animals. Such a budding or division in the embryo may indeed be looked upon as somewhat akin to the development of buds or gemmae in the Porifera or the statoblasts of certain fresh-water Bryozoa which normally develop double embryos directly from a germinal body. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 77 There may also be a kinship detected in the tendency of Hydrozoa and Scyphozoa to reproduce themselves in this way, especially the sedentary or colonial forms. The tendency of star-fishes to bud out branches from their arms is another illustration of the same thing, and it has been recently shown that under exceptional conditions the point where an arm of a star-fish is budded oflT may mark the point near where a new mouth and a full complement of arms will appear so as to develop a complete new individual. As we rise in the scale of organization, this tendency to regener- ate lost parts becomes more and more restricted to the reproduction of peripheral parts only, but the tendency to produce monstrosities in the shape of more or less completely fused embryos, due to dis- turbances of development, remains in full force. Not only is this the fact, but I also believe that I have indisputable evidence that an embryo may undergo partial development within the uterus of a mammal, when it will be arrested and actual histolysis with conse- quent destruction and absorption of the embryo takes place. More remarkable still is the conclusion reached by von Jhering that certain Armadilloes normally produce several young from a single fertilized ovum. His view being that in no other way can we explain the envelopment of the entire litter of young of some of the species of these animals in a common chorion. In this opinion, I take it, von Jhering has the support of the opinion of authorities as eminent as von KoUiker and H. Milne-Edwards. When certain of the vertebrates such as fishes, batrachians and reptiles are injured after adolescence is reached, they retain to a limited degree the power to reproduce lost parts. Not only do they possess this power, but they tend to reproduce such parts in dupli- cate, that is, the peripheral part is reproduced double, and as if diverging from the point of mutilation. An instance of this that I recall is the case of a fine Amieva^ in the collection of the Academy of Natural Sciences of Philadelphia, had its tail torn oflT, and from the point where the tail was removed two new tails were being produced. Other equally striking instances are the toes of Salamanders that have been injured. The Axolotl and its kindred, the species of Amblydorna, do the sarae thing when the toes are injured or nibbled oflT by fishes ; the tendency is to reproduce them in duplicate, or even in triplicate. The same thing liappens when a fin-ray is injured or torn out in the fins of a Malacopterygian fish : the actinotrichia tend to be reproduced in manifold and radiate 78 PROCEEDINGS OF THE ACADEMY OF [1893. from the stump of the old ray in a divergent fashion. This fact I have repeatedly observed, as well as the regeneration, i?i situ, of the scales, where they have been forcibly removed from the fish by accident. A case of this kind I traced and described some years ago, the subject being a fine specimen of the mirror-carp that had lost one of the large scales of the lateral line. In this case, how- ever, there is no duplication of the scale during its regeneration. It is also a notorious fact that when extra toes or fingers are developed in the human subject, or in a mammal, they tend to become hereditary. And the same seems to be the case with birds,, in the instance of the Dorking fowl amongst domestic breeds. It is my belief from the evidence presented above that such supernumerary digits have been in the first place produced by disturbances during segmentation or karyokinesis. While the embryo was developing its digits in such higher forms and that such disturbances have been registered, so to speak, as part of the hereditary tendencies of the organism, and have thus been handed on to offspring as develop- mental tendencies. The tendency to reproduce supernumerary toes in the cat is well-known. The same tendency is shown in the dispo- sition to reproduce extra thumbs or toes in certain human families. The most extraordinary of these duplications is however presented by the double or fan-tailed races of Japanese Gold-fishes, where the duplication sometimes extends even to the anal fin, so that I have elsewhere been tempted, upon the evidence presented by Dr. Watase as to the development of these fishes, to put in a plea for the actual realization of an eight-limbed vertebrate, a thing against which the learned Professor Haughton, of Dublin, has argued with his wonted acumen, in a still earlier paper touching the utility of the four- limbed condition of the higher vertebrates. I believe, however, noAV that the key to the mystery of the pro- duction of the double-tailed gold-fishes is within our reach in the light of the evidence presented above, that we can guess how the Japanese went to work to produce their singular breeds of Cco'assiitf' aurafiis. I believe, in short, that their practice was very simple, and that they have probably antedated the practical appli- cation of the facts of experimental embryology, as known in Europe and our still more western civilization, by several centuries. Since the Japanese records of some of these breeds are very old, as well as the fact that the work of the Marquis de la Savigny, figuring the breeds of these fishes, was published in 1790, we can infer for them an antiquity of, at the very least, a couple of centuries. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 79 Now as to how the Orientals accomplished the production of double-tailed forms of fishes. I believe they did this by taking the eggs of the normal species of gold-fishes and shaking them, or dis- turbing them in some way, as did Professor Weber with the eggs of the pike. They would thus get some complete double monsters, some with two heads and a single tail, and some with double tails. Mani- festly the complete double monsters would be unlikely to survive. Those most likely to survive would be those with only a duplication of the tail. These being selected and bred would in all probability hand onward the tendency to reproduce the double tail, a tendency which could become very fixed and characteristic if judicious selection were maintained by interested fanciers and breeders, such as are said to exist in Japan, where these fishes of the finest double- tailed races command high prices amongst the wealthy and culti- vated classes. If the remarkable peculiarities of the Japanese Gold-fishes were produced as suggested above, and there seems to be no more likely method of their origination, the whole question of the inheritance of mutilations is reopened from a totally new point of view, and one that cannot be assailed by Weismann and his following with much show of success from their present attitude toward these questions. It is clear, however, that we have here a most promising field for experimental inquiry and one that should be at once cultivated in a practical way. That the direction of the regeneration of lost parts may be affected by the plane of mutilation is sufliciently well attested by the exper- iments of Barfurth on the tails of tad-poles, some of which I have successfully repeated. If the tip of the tail were snipped ofl^ exactly at right angles to the axis of the body, the tail w^as regenerated of the normal form and straight backward. If at an acute angle, regeneration took place so that the new tip was directed either upward or downward, according as the inclined, regenerating cut surface looked upward or downward. Such facts cannot be dis- missed as useless in connection with the problem of inheritance in general, if they have any bearing upon the questions raised in con- nection with the inheritance of mutilations as viewed in the preced- ing discussion. It is not unlikely that Barfurth's results do have some bearing upon these questions as here viewed. If the plane of mutilation or line of removal of digits affects their direction of growth, as seems likely from Barfurth's and my own experiments, 80 PROCEEDINGS OF THE ACADEMY OF [1893. we know to a certainty that there is only one avenue for the access of new material during the process of regeneration of a digit for example, and that is its proximal or basal portion. Through this basal portion alone can new material reach the digit to build up its distal parts. If growth and its accompanying karyokineses were interfered with in any way across a narrow line over the stump, the regenerative energies would be caused to manifest themselves on either side of that line, and the result would be a tendency to repro- duce the digits in duplicate beyond the point of mutilation, and in a divergent fashion from the basal area through which alone new material could find access by intussusception during the process of regeneration. We consequently get a mechano-physiological expla- nation of why it is that doubly reproduced distal parts tend to diverge from each other radially. The same principle, together with concrescence, may be invoked, as it has been in another form, by Rauber," to explain the degree of fusion of double or triple monsters produced by shaking mesoblastic ova during their early blastodermic stages of development. But Rauber's explanation must in this case be supplemented by a consideration of the physical laws of the interfacial and free surface- tensions which condition growth during the development of a thin blastoderm in a meroblastic egg, making, for self-evident physical reasons, the production of completely separate embryos well nigh an impossibility, even by shaking or otherwise interfering with development. Even if separate germinal disks were developed on a telolecithal egg, there is every reason to believe that, as segmenta- tion proceeded, the two resulting blastoderms would become fused by their edges as the latter advanced over the yolk and approached each other as they necessarily must in order to increase, as they do, in a geometrical ratio, their power of appropriating the stored nutri- tive mass of yolk. On a priori grounds, and for mechanical reasons, therefore, the complete separation of the germinal matter of a large-yolked meroblastic egg is impossible. The total separation of the two first blastomeres of the equally segmenting, holoblastic eggs of echinoderms and Ampkioxus, on the other hand, is easily accom- plished by mere violent mechanical interference, so that completely distinct and separate, but smaller, embryos are easily obtainable if such separated blastomeres are allowed to develop under favorable conditions. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 81 As stated in the earlier part of this paper, the regenerative power seems, in low and primitive forms, and also in the very early stages of the highest, as shown by von Jhering in the development of Armadilloes, by what he calls temnogeny, or normal division and complete separation of the cells of the fertilized egg, to be most completely represented in the early blastomeres or the products of the early segmentations. In the next grade of organic types, Porifera and Coelenterata, there appears to be a wider exten- sion upon the whole organism and its parts of this regenerative power. In bryozoa and echinoderms there is still in many forms more or less of this regenerative power distributed throughout the organism, but as specialization proceeds it seems to become less marked, and if there is disturbance of the mode of development of the Bilateralia, besides the apparently normal consecutive or linear gemmation as in Monotus, Mijrianida and Aidolytus, there is devel. oped a tendency to double the axis so that branched or coherent double individuals arise. This reaches a most remarkable expres- sion amongst Syllid worms, as worked out by Professor Mcintosh, and may even extend to an early stage, as in the case of the produc- tion of double embryos in Lumbriciis, according to Kleinenberg. In both the arthropod and vertebrate series disturbances of early embryonic development, affecting the order and relations of the karyokinetic processes in the blastoderm, are productive of double monstrosities variously fused, according to a law which has been to some extent defined by Rauber. As we proceed in our review of the successively higher groups we find that this purely regenerative power becomes less and less marked. In some worms, for example, the head may be regenerated if cut off. It is doubtful whether this would be possible with even the lowest vertebrate. In the vertebrates and arthropods or highest Bilateralia, the regenerative power is reduced to the power of repro- ■ducing lost digits or entire appendages, as in Crustacea. In verte- brates it is finally restricted in fishes, batrachians and reptiles to* the regeneration of the tail or the distal parts of the extremities in the adult, and in the highest of these series, namely, birds and mam- mals, the power of the adult to regenerate lost distal parts of the extremities is also lost. Nevertheless, there remains in the tolerably advanced embryos of these forms the power to respond in a remark- able way to disturbances of the normal hereditary or regenerative processes involving the distal parts of the extremities, such as the 82 PROCEEDINGS OP THE ACADEMY OF [1893. digits. The regenerative powers therefore seem to become dimin- ished with the specialization of a type, and to be manifested last of all in the distal ends of the extremities. The most marked changes may occur in the way of duplication, triplicatiou, etc., of the axis, even in the highest types, provided the development or processes of segmentation are disturbed early enough, and in some definite way. The conclusion which is warranted from the whole of the foregoing is that the regenerative power of organisms disappears as we rise in the scale of organization, last oj all in the peripheral extremital parts. A further observation is justified, which is, that the power to produce monstrosities or congenital aberrations of development due to external disturbances of segmentation, during growth, diminishes in the higher forms pari passu with the advance in development. Finally, it may be affirmed with much show of probability that aberrations of development produced by disturbances of the processes of segmen- tation during growth, may become hereditary, as illustrated by the probable inheritance of partially duplicated axes in the tails of Japanese gold-fishes, or of supernumerary digits in many mammals and in Man. How such new parts, originated as here supposed, can transmit to the ova of the parent body, of which they form a part, a tendency to cause them ( the new characters ) to reappear in the off^spring developed from such ova or germs, cannot be explained without supposing that the new part of the body of the parent influences at a distance the characters and potentialities of the germinal matter produced by it in its gonads. The difiiculties in the case of the partly double body of the Japanese Gold-fishes are peculiar, in that we have to assume that hereditary tendencies are transmitted from a parent body and part of another of each sex, making in all, ten- dencies transmitted from two bodies and parts of two others, in the course of the ordinary sexual reproduction of the double-tailed species, since there cannot be the slightest doubt that, in this case, we have to deal with partially double monsters (as is proved by their morphology), with normally developed reproductive powers. I confess to an utter inability to see how this can be done by means of gemmules, the oldest hypothesis of heredity, first formulated by Democritus, then restated in a more modern form by BuflTon, then by Erasmus Darwin in the Zoonomia, and lastly by Charles Darwin. This doctrine therefore has a very respectable pedigree, but it is strange that none of the later writers credit their predecessors with. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 83 having entertained similar opinions. But to recur to my point, it is clearly certain that the partially double body of the parent in this case must have influenced the germs it inclosed at some time in the history of the race, or at the time the latter was originated by the Orientals. The first partially double, monstrous pair of gold-fishes to have offspring must have been reared somewhere in the East ; whether in Corea, China or Japan does not matter. The fact that they reproduced themselves is indisputable. That they were first produced by artificial interference with, or mutilation of the normal processes of their early development becomes, in the light of what has been said above, a conclusion of the utmost probability. Weis- mann and his followers can take either horn of this dilemma. The inevitable conclusions are : first, that new parts of the parent body at a distance do at once, in the first generation, influence the germ- cells inclosed by such a parent body ; secondly, the i^robability of the inheritance of the effects of certain mutilations, injuries, interfer- ences or displacement of parts, during the early stages of develop- ment, amounts almost to a certainty. Moreover, whereas the separation of the early cells or blastonieres in certain eggs, such as those of Armadilloes, Sea-Urchins and the Lancelet and Frog is possible, the egg in these cases being essen- tially holoblastic at the time of the first two cleavages, two or more completely separate embryos can be developed. The conditions of development, it must be borne in mind, in the higher series, where a blastoderm is developed, closely and firmly adherent to the very large, nutritive yolk, are very different from the foregoing. So dif- ferent indeed, are the conditions of development in these latter mer- oblastic forms that it would be extremely improbable that entirely separate and multiple embryos could be developed from their ova. At most only such mechanical disturbances would be possible as would lead to a more or less complete duplication, triplication, etc. of embryos. That the effects of such embr3'onic mutilations or interferences may be hereditarily transmitted will hardly be admit- ted by the anti-niutilationists, but to evade the force of these facts is impossible. The coherence of the embryos together in meroblastic eggs, con- ditioned as it is by the interfacial and free surface-tensions between the blastoderm and yolk, is, it seems to me, plainly indicative of the indisputable conclusion that mutilational influences operating upon meroblastic ova are themselves influenced by mere physical condi- ^4 PROCEEDINGS OF THE ACADEMY OF [1893. tions and. forces, and that even these leave a reminiscence of tlieir effects upon the germs, the development of which they thus indi- rectly affect. What again shall be said in such cases of the effect of such external or physical agencies or conditions in modifying the development of future generations, as seems to be proved by the history of the domesticated races of Japanese Gold-fishes? Weis- mann must now own, if the preceding views can be sustained, that lie is beaten upon his own ground, and also admit that he has been in error from the beginning as to the non-transmission to the germs of characters that have been acquired by the body of the parent. The domesticated races of Japanese Gold-fishes outstrip every known form of domesticated animal in the extent to which they have been modified, and it is therefore strange that Mr, Darwin should have devoted so little consideration to them in his works. In one of his botanical works Mr. Darwin makes the suggestion that the bilateral halves of the Bilateralia may have arisen by longitudinal concrescence of two similar individuals of opposite sex. This suggestion of his, as to the origin of the bilaterally sym- metrical condition, may be dismissed as exceedingly improbable and unfortunate, and as in direct conflict, moreover, with the known mode of the development of monsters with double axes. Such mon- strous races, as is proved by the morphology of the adult Japanese Gold-fishes, their known analogies to the development of double vertebrate monsters, have been produced almost beyond a shadow of doubt by mutilational interference with the early processes of nor- mal development, and this monstrous mode of development has become hereditary. The procedure by means of which the Orientals originated their peculiar races of Gold-fishes I believe was more exactly as follows: After the blastoderm had spread over about one-third or more of the surface of the yolk, the eggs were shaken or violently disturbed. This proceeding would cause the production of one or more new embryonic axes at the rim of the blastoderm near the original axis, but the new axes would not develop a head, but would, as a result of the operation of the principle of concrescence, soon fuse with the caudal end of the original or first-formed embry- onic axis. This would cause a doubling, more or less complete, of the caudal end or urosome of the embryo. In this way it may be siipposed that the partially double urosome of these singular fishes 1893.] NATURAL, SCIENCES OF PHILADELPHIA. 85^ was developed, so far at least as to duplicate the hypural system of bones of the tail, and consequently the tail itself, while this doubling would also manifest itself farther forward so as to sometimes double the anal fins as well. The caudal part of the notochordal axis i& rarely doubled, though there is an evident tendency to do so in some individuals. The great exaggeration in the development of the fins in Japanese Gold-fishes, especially the caudal, is, however, not wholly accounted for by the theory of the inheritance of tendencies toward monstrous development. Nor is the obvious degeneration of certain parts of the muscular system in some of the races thus accounted for. Nor can we again account for the differences in the relative lengths of the intestine in the different races on such a hypothesis. Only one structure, the squamation and the number of myotomes, seems to have remained constant in the course of the great modifications which these fishes have undergone. I find that the number of rows of scales in the lateral line in all the races I have studied, presents practically no variation ; that is, the number of scales in the lateral line varies only from 25 to 26. The number of myotomes is also constant in all the races, and corresponds to the number of transverse rows of scales. In order to make the facts stated above somewhat more easy of apprehension, I have tabulated the result 'of a series of careful measurements, based upon tliree races, viz : (1) the normal or common gold-fish, Carassius auratus ; (2) a long- bodied double-tailed variety of great beauty, which has been reared in the aquaria of Dr. W. H. Wahl, who has kindly let me have some dead individuals, for study; (3) a short-bodied double- tailed race with a very protuberant abdomen, which were imported from Japan, and of which dead examples were furnished me by Mr. W. P. Seal. I found that the head in all cases was the least variable part of the animal. I have accordingly regarded it as a standard of com- parison in a general final table. The following tables will explain themselves, and give absolute measurements in millimetres of the same parts of the three races in parallel columns. By urosome is meant the part of the trunk behind the body cav- ity, and between the latter and the base of the caudal fin. 1 have compared the musculature of the abdomen and urosome to a frus- tum of a cone with an elliptical cross section. In this way it is possible to show, taking the absolute measurements in connection -86 PEOCEEDINGS OF THE ACADEMY OF I. [1893. Total length of head, body and urosome. Length of body. Length of head. Length of intestine. Width of end of uro- some. 1 Common race. 90 mm. 62 mm. 28 mm. 364 mm. 15 mm. 2 Long-bodied Japanese double - tailed 74 mm. 51 mm. 23 mm. 213 mm. 10 mm. race. 3 Short-bodied Japanese double - tailed 47 mm. 28 mm. 19 mm. 226 mm. 7 mm. race. ^th other facts, that there has been a process of degeneration at work in reducing the proportional volume of the musculature of the body and urosome in the double-tailed races. Table II gives the height of this frustum of a cone to which I have compared the musculature of the body, as well as the major diameters of the base and apex of the frustum in millimetres, for each race in absolute measurement, II. Length of caudal fin. Distance from vent to caudal. Width of base of muscular frustum of a cone. Height of Width of muscular a p e x of frustum, muscular frustum of a cone. Common race. 36 mm. 25 mm. 37 mm. 62 mm. 15 mm. Long-bodied •Japanese doub- le-tailed race. 80 mm. 19 mm. 28 mm. 51 mm. 10 mm. Short-bodied Japanese doub- le-tailed race. 36 mm. 10 mm. 23 mm. 28 mm. 7 mm. In a third table I have attempted to represent the proportions of the several parts to each other, but from tables I and II, I obtain •data for a more general and final fourth table in which the individ- uals are supposed to be of the same age, and more nearly of the «ame size and weight than was the material at my disposal. 1893.] NATURAL SCIENCES OF PHILADELPHIA. III. 87 Ratio of he a d to length o f intestine. Ratio of total length to length of intestine. Ratio of length of the body to the length o f the intestine. Ratio of width of urosome to total length of head, body and urosome. Ratio of total length of the head, body and urosome to the length of the tail. Common race. 1:13 1:4-45 1 : 5-85. 1:6 2-5:1 Long-bodied Japanese race. 1 : 9-25 1:2-85 1:4-2 1:7-4 1:8:3 Short-bodied Japanese race. 1 : 11-75 1:4-6 1:8 1 : 6-71 1-33 : 1 Taking the head as the least variable portion of the three races, and assigning to it an arbitrary value of 50 mm. in a hypothetical individual by dividing the actual lengths of the other parts in mil- limetres by their own length of head in millimetres, then multiply- ing this product by 50, I get a new set of values in which the parts are in the proportion of the preceding table, but in which the indi- viduals are, in the case of each race, of about the same size, age and condition of volume, and consonant with the modifications that have been suffered by each one. This table is given below, and from it it is possible to plot the outlines of the three hypothetical frustums of cones that will represent approximately the condition of development of the musculature of the body and tail of the three races as seen from the side. IV. Common race. Long-bodied Japanese race. Short-bodied Japanese race. Length of intestine. 650 mm. 4625 mm. 587'5 mm. Length ofhead. 50 50 50 Height o f frustum. 110-7 mm. 110-8 ram. 73-65 mm. D i a m eter of major axis of base of frustum. 66-2 mm. 65 mm. 61-3 mm. D i a m eter D i s t a n c e of maj o r of anus from ax is of apex base of cau- of frustum, dal. 24-3 mm. 21-7 mm; 18-4 mm. 42 mm. 41 mm. 26-3 mm. PROCEEDINGS OF THE ACADEMY OF [1893. These tables aud the appended dia- gram based upon them, it seems to me, make it tolera- bly certain that there has actually^ be e u a marked degeneration in the relative p r o p o r - tional development of the volumes of" the musculature of the body and uro- some or tail in two of the three races examined. 0th e r facts, however, for- tify this conclusion very strongly. The most important being the fact that the vertical rows of scales just behind the abdomen, on the sides of the urosome of the short-bodied race, overlap each A. Outline of frustum of cone representing the mus- O^ner I a r more culature of body and urosome of common race of Gold- extensively than do carp. B. Same of long-bodied Japanese race, reared those in the other byDr. Wahl. C. Same of short-bodied Japanese race. two. When we come to examine the muscular somites underlying these rows of greatly overlapping scales in the short-bodied race, we actually find them markedly shorter than those some distance behind, or those some distance in front of them. This seems to me to prove conclu- sively that there has been actual degeneration of the muscular sys- tem of the body or trunk, and that this degeneration is especially well marked in the short-bodied race. The intestine in the latter is also found to be proportionally longer than in the normal, common,. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 89 or in the long-bodied, double-tailed races. This increase in the length of the intestine is also indicated by the very protuberant abdomen of the short-bodied race. This short-bodied race, with a protuberant abdomen, I am informed by breeders, is a very vora- cious feeder, thus not belying the indications of its large abdomen and proportionally long intestine. It is also probable that the bodies of the vertebr;* are shorter in the short-bodied than in the long-bodied races. This point I have, however, neglected to determine, I believe, in short, that the degenerative changes in the muscular system of the Japanese Gold-fishes is connected with their continued restraint to small aquaria for many generations, and that their mus- cular system has degenerated through disuse. That, on the other hand, the failure to be able to expend energy in the production of motion of the body in the water has reacted in other ways upon their organization, and especially upon the growth of the fins. This has gone on until, in some of the races, it would actually be possible to envelop almost the entire head and body in the enormous double caudal. In fact, these members grow so long that they become an actual hindrance to rapid swimming, and are of less use in pro- pelling the fish in the water, so that their swimming becomes very slow, and seemingly performed with some difficulty as compared with the normal form. All the fins partake of this tendency to become extended ; the pectorals enlarge and lengthen, and the dorsal, in some races, becomes so long that it falls over and over- hangs one side of the body. Fish-culturists also tell me that it is useless to try to keep these races with other species of fishes in ponds, because the more active carnivorous forms will soon bite off and destroy the long, graceful, and lace-like caudals of these help- lessly modified Japanese races. These races have been so modified by man's agency, that they have become absolutely unfitted to suc- cessfully battle for existence, if left to themselves. Their sluggish habits have been purposely cultivated by Oriental fish-fanciers. To such an extreme of sluggishness have they been brought, that, owing to their monstrous development, they are some- times no longer able to maintain their equilibrium in the water, but stand on the head or tail in the very small aquaria, in which they are kept, and in which they would become asphyxiated were it not for the precaution taken by the Japanese to introduce into the same 7 so PROCEEDI>'^GS OF THE ACADEMY OF [1893. aquarium small, harmless, but very active fishes of other species, in -order that the water be kept circulating, and thus aerated for the Jbenefit of the helplessly modified, but most valued tenant. These circumstances give, it seems to me, a clew to the explana- tion, not only of the degeneration of the musculature under domes- tication, owing to its enforced disuse, but also some indication of what are the causes of the extension of the fins. The material saved from expenditure in muscular effort may be expended in growth iu another direction, and the most advantageous would be that which would increase the surface of the fins, and thus render them useful in dermal respiration. The large vessels and numerous capillaries in the huge tails of very fine specimens of the Kinyiko race, that I have seen, indicate that the caudal fin may possibly 5erve in a very important way as an adjunct to branchial respira- tion. The question therefore arises, have not the immense fins of the Japanese double-tailed gold-fishes been developed partially in physiological response to artificial conditions of respiration, that were not as favorable as those enjoyed by their wild congeners? That the dorsal, anal and caudal fins may be so modified as to min- ister in an important way to the needs of respiration, is proved by the development of the richly vascular and exaggerated vertical £ns of the embryos of fcetal Embiotocoid fishes, as long ago shown bv Blake, and fully confirmed and elaborated in greater detail by the writer. It is also a remarkable fact that the fins and tail of the larvie of the •double long-tailed races do not show such characters at once, but it is not until long after thelarval stages-are passed, that the breeder can be certain of rearing a specimen with a fine long tail, from any given young fish. The fishes are usually upward of two inches iu length before the breeder can be pretty sure that the young or half-grown individuals will develop a great length of tail. This fact shows that the long tail was originally acquired very late in ontogenetic development, and is not a larvally apparent differentiation. This circumstance is also unique amongst fishes, and for that matter, almost the exact reverse of what usually takes place, since the young of many marine fishes have certain parts of the fins very greatly produced, only to be absorbed before adolescence is reached. This is the case with the larvie of Lophim and Fierasfer. Only amongst higher animals do we find secondary sexual characters produced at a late period of growth, such as the deciduous horns of the Deer 1893.] NATURAL SCIENCES OF PHILADELPHIA. 91 family, or defensive organs, such as the horns of the ox and ante- lope families, which are produced at a relatively late period. The fact that the very long fins of the full grown individuals of the double-tailed races of Gold-carp are only fully developed at a very late period of the growth of the animal, is in harmony with the view that the hypertrophy of those organs is associated with a correlative degeneration of the muscular system of the trunk, and a possible use of these structures with their great amount of surface as respiratory organs, in the restricted and badly aerated tanks and aquaria in which they have been bred for centuries. Since the above was written, Mr. W. P. Seal has sent me a series of the "telescope-eyed" double-tailed race of Gold-carp. This, together with the materials previously supplied by the same gentle- man and Dr. Wahl, enables me to greatly extend my comparisons and also, as will be seen below, to add some very remarkable facts to our knowledge of these singular domesticated races of fishes as com- pared with their wild congeners, long since introduced into the Schuylkill, and now native to that river. The most astonishing peculiarity of the " telescope-eyed " race is the development of the eyes. The latter are very much larger pro- portionally than in the common or in any other races, so that the eyes actually protrude from the orbits in a most grotesque manner. The size of the eyes on opposite sides of the head even seem to vary somewhat, and in the extent to which they protrude from the orbit. In some specimens the eye-balls are a third more in diam- eter across the equator than in either the common or the other double-tailed races. A broad band or ring of integument passes all round the equator of the eye-ball joining the cornea distally and the margin of the orbit proximally. The most surprising tact of all, however, is the shape of the eye- ball in the telescope-eyed race, in that the eye-ball tends to become greatly elongated in the direction of its optic axis. Sometimes the diflTerence between the axial and equatorial diameter is as much as three millimetres, constituting an extremely myopic form of eye-ball. The form of the eyeball in the common race is flat or hypermetropic in character. A gradual passage from the hypermetropic form of eye-ball to the myopic is shown in the following table, as based upon actual approximate measurements of the eye-balls of indi- viduals of the three races. 92 PROCEEDINGS OF THE ACADEMY OF V. [1893. Races. Total length of specimen. Equatorial diame- ter of eye-ball. Axial diameter of eye-ball. Common. 130 mm. 7 mm. 5 mm. Short -bodied. 55 mm. 5 mm. 4 mm. " Telescope-eyed." No. 1. 63 mm. 6 mm. 6 mm. No. 2. 70 mm. 6 mm. 9 mm. The size and shape of the globular lens in the "telescope-eyed" race is not appreciably different from that of the other races with, smaller eye-balls. It would therefore, seem impossible for the image formed by the lens of a distant object in the " telescope eyed " race, to be thrown upon the retina at all, consequently the condition is one of near-sightedness, or of an optical adjustment for very near objects. The conditions of life of these races, in small tanks or aquaria, where they are bred under conditions of the great- est protection from man, would in their restricted quarters actually foster the development of near-sightedness, and any variations in that direction would actually tend to be preserved. There is a con- dition of disuse also to be taken into account in this process, since these fishes no longer need their eyes with which to watch the approach of their enemies, but only to look out for their food, which is supplied to them by their human friends and protectors.- To what extent this factor has been of service in altering the shape of the eye-balls, it is of course, as yet, impossible to state. The pre- ceding table V, however, makes the gradual passage from the hyper- metropic or flat eye of the normal race to that of the myopic or long eye of the " telescope-eyed " race sufficiently obvious as the series of measurements given of the eye-balls of the different races proves. The fact that a race of fishes may become myopic, as would seem to be indicated by the foregoing data, is most surprising, aud affords a case parallel in some respects with that of the human race itself; but in the case of these fishes the myopic tendency has probably been further developed by the intentional selection of myopic indi- 1893.] NATURAL SCIENCES OF PHILADELPHIA. 93 vidiials by breeders and fanciers for breeding purposes. A near- sighted fish is certainly au anomaly, and the name " telescope " fish, in allusion to the protruding eye-balls, becomes a misnomer, since the form of the eye is distinctly myopic .and short-sighted, and not hypermetropic or far-sighted as required of an optical organ having telescopic capabilities. These facts go still further to support my assertion that these races of Gold-carp are the most profoundly modified of any known race of domesticated animal organisms. No •other domesticated animal, as far as I am aware, shows such pro- nounced evidence of becoming myopic. These " telescope eyed " fishes also show evidences of mal-develop- ment of the dorsal fins, and a tendency to have the vertebral col- umn curved downward behind in an abnormal way, producing the appearance of a " hunch-backed condition." Such defective devel- opment of the dorsal together with a hunched back is also not infrequent amongst the other short-bodied and long-bodied double- tailed-races. Such defective development of the dorsal, accom- panied by a hunched back, is also found in partially monstrous trout, some of which have been recently figured by a writer in Forest and Stream (vol. xxxix, p. 562, 1892), from specimens sup- plied by Mr. Creveling, which measured from 6? to 8 inches in length. Since these changes in the development of trout are well known to be associated with injuries inflicted during the early stages of development, the case that I have made out for the origin of the double-tailed races of Gold-fish is thus markedly strengthened by similar facts derived from an entirely distinct family, the Sal- monidse. All of the foregoing evidence consequently compels me to abandon the view entertained by me in an earlier paper^ respecting the origin of the double-tailed races of Gold-carp, in which it was suggested that the doubling of the anal and caudal was a reversion to a remote ancestral condition in fishes, in which paired lateral-fin folds extended for the whole length of the body. This view involves the conception that the single caudal of existing fishes was primi- tively a double organ, which has been produced by the concrescence of a pair of lateral caudals, a doctrine which it is quite impossible to reconcile with the morphology of the tails of normal fishes, or that of the tails of the double-tailed races of Gold-carp. What to my mind makes this view still more improbable is the fact that I find the double tails of these " telescope-eyed " forms completely divided ^An eight-limbed Vertebrate. American Naturalist, September, 1887, pp. 862- 863. 94 PROCEEDINGS OF THE ACADEMY OP [1893. up to the vertebral axis, so that, morphologically speaking, there are parts of two distinct axes, or individuals, present in each speci- men. This evidence, together with that respecting the defective development of the dorsal, and the tendency toward a hunch- backed and deformed condition, perfectly parallel to the conditions seen in traumatically deformed trout, seems to me to almost conclu- sively prove that the double-tailed races of Gold-carp have arisen in the first place as a consequence of injuries inflicted during the early development of the eggs and embryos, and that the effects of these embryonic traumatisms have become hereditarily transmissible, as the facts seem to indicate. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 95 THE VASCULAR RESPIRATORY MECHANISM OF THE VERTICAL FINS OF THE VIVIPAROUS EMBIOTOCID^. BY JOHN A. RYDER. The young surf-perch, Ditrema laterale, from which this figure i& drawn, measured about twenty-three millimetres in length. It was one of several which were removed from the saccular ovary of the parent, each young fish lying lengthwise and disposed so as to bring the enormously expanded vertical fins into contact with the wide ovarian folds and the sides of the ovarian walls. As can be seen from the figure, the lateral area of the vertical fins quite equals,. if it does not exceed, the lateral areas of the body. In fact, the dorsal is as high as the body is deep. In the same way the caudal fin is as wide at its widest part as the body's greatest width. The total length of the caudal is not far from a third of the total length of this larval stage. Another feature which distinguishes this young fish from the young of all other species is the highly vascu- lar condition of the inter-radial membranes of the vertical fins. This vascularity is not only obvious when the object is viewed with a transmitted light, but also in sections. The most marked devel- opment of capillary vessels is found in the flattened lobes with which the fins are bordered. Fourteen very distinct lobes with deep notches between them are found along the margin of the tail ; about 96 PROCEEDINGS OF THE ACADEMY OP [1893. twenty-eight smaller lobes can be counted on the margin of the anal fin. About eighteen well-marked lobes presenting the highly vas- cular character of the others, already mentioned, are found to bor- der the dorsal fin, the spaces between the anterior nine rays of which, unlike the others of the same fins, are non-vascular. In cor- respondence with this highly vascular condition of the marginal lobes and the inter-radial spaces in these three sets of fins, there is found to be developed a system of three sets of large arterial and venous trunks which send the blood to and carry it away from the vertical fins. The caudal termination of the caudal vein and aorta supply the caudal fin. In the figure it is mainly the venous trunks which are represented. It is seen that at the point where the caudal vein enters the caudal fin it divides into two very large trunks, such as are not met with in any other known type of fish of the same age. One of these trunks passes in a dorsal and another in a ventral direction, carrying away the blood from the dorsal and ventral halves respectively of the caudal fin. The number of branches which pass from the two trunks mentioned correspond very closely to the number of inter-radial spaces. A second system of vessels, much slighter in caliber after death than they probably were during life, is seen just a little way anterior to the two large venous trunks already described. These are probably the dorsal and ven- tral branches of the arterial system into which the posterior termi- nation of the caudal portion of the aorta divides in order to supply the caudal fin-membranes with arterial blood. The radiating venous and arterial inter-radial vessels pass quite to the margin of the caudal, where they form vascular arcs around the edges of the flat vascular lobes already described. From within this vascular arc to the point of insertion of the caudal rays the inter-radial membrane is found to be traversed by a close plexus of capillary vessels. This plexus is excavated in a connective tissue which lies between the epidermis of the opposite sides of the fin. Four sets of vascular trunks pass from the dorsal ; of these the three posterior are the most strongly dev^eloped. They take their rise directly from the caudal vein and caudal portion of the aorta on the dorsal aspect of these vessels. Each of these vessels upon reaching the base of the dorsal divides into an anterior and poste- rior trunk. Each of these trunks gives off" in a vertical direction nearly at right angles to themselves a series of inter-radial vessels. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 97 The posterior trunk gives off the greatest number of these inter- radial vessels. The anterior main trunk gives oft' four inter-radial "vessels. The marginal lobes are highly vascular, although not so wide nor so long as those of the caudal fin. The aual fin receives its vascular, supply through four sets of large trunks coming off from the inferior aspect of the caudal vein and aorta. These trunks pass nearly straight downward toward the margin of the anal, their distal portions only being slightly tor- tuous. The posterior or fourth trunk, as are all the others, is bifur- cated at the base of the anal into an anterior and posterior branch much in the same way as the similar vessels divide in the dorsal. The fourth trunk gives oft" the greatest number of inter-radial ves- sels. The second and third give oft' a smaller number of such inter-radial branches. The first anal trunk appears to supply a portion of the inter-radial spaces at the anterior edge of the anal fin while branches moi'e or less intimately associated with it, or derived from it, pass to the greatly hypertrophied hind-gut. At any rate the vascular supply of this curiously hypertrophied part of the alimentary tract is given oft" close to this vessel. In whatever way the blood passes through the walls of the hind gut H. G. ; it finds its way at last to a large vascular trunk marked S, lying on the ventro-anterior face of H. G. This large vessel S is evidently the homologue of the sub-intestinal vein in other fishes. At the anterior end of S large trunks diverge from it, pass around the mid gut and find their way into the liver. These trunks repre- sent the portal system. Little that is noteworthy can be made out from a transparent view in regard to the way in which the blood reaches the heart from the jugulars. Sections indicate that the Cuvierian ducts are very spacious, more so than is represented in the diagram. The ventricle of the heart H is well developed with thick muscu- lar walls. The bulbus arteriosus is a simple thickened muscular tube extending forward from H. The homologies and relations of a large trunk ascending obliquely forward and upward, then bend- ing downward and forward, probably meeting its fellow of the opposite side before it traverses the median face of the mid brain is diflacult to determine. A smaller trunk descends from the region over the body toward the eye and prol)ably joins the ophthalmic vessels in that region to finally empty into the basilars and jugulars which pass backward toward the origin of the Cuvierian ducts. 98 PROCEEDINGS OF THE ACADEMY OF [1893^ The membrane bones of the skull are already fairly well developed, as are, in fact, the membrane bones throughout the body generally. The vertebral rings of the vertebral column are already defined, and are separated from each other by considerable inter-vertebral spaces. Their dorsal and vertical outer margins are gently concave. The ribs, the neural and haemal arches are developed and the com- plicated musculature of the caudal fin is already well marked. The hypural pieces of the caudal are well-developed in cartilage and a partly membranous matrix. The pectoral fins are already well- developed but present as far as I have been able to make out no such vascularization as the others. The ventrals are still small and undeveloped. The lateral line system does not seem to be strongly marked at this stage ; the small round pore behind the eye repre- sents its connection with the exterior. The air bladder is devel- oped and occupies considerable space at the point P in the body cavity. Just in front of the air bladder is a large highly vascular mass representing the Wolffian body or kidney. The glandular portion of the Wolffian body is thus seen to be quite anterior in position. Cross-sections show that Wolffian ducts are present behind the region of the Wolffian body as a pair of simple longitudinal canals. These ducts pass backward parallel with each other as far as the downward flexure of the hind gut H G. At this point they suddenly bend downward and gradually converge so as to meet just before opening to the exterior between the hernia-like protrusion of the lower portion of the hind gut and the anterior margin of the anal fin. As already stated the hind gut is very much enlarged in trans- verse diameter, as may be seen from the accompanying figure. Upon being cut open it is found to be filled up with villous or fila- mentous productions of its lining mucous membrane. These villi tend to be flattened, and with the widest portion of their bases extending parallel with respect to each other and in conformity with the length of the intestine. The anal opening A is found on the posterior face of the hernia-like protrusion of the abdominal wall caused by the hypertrophied hind-gut. The mid-gut is separated sharply from the hind-gut by a pyloric constriction just a little below and behind P as shown in the diagram. The mid-gut or gastric portion of the intestinal canal presents no very unusual fea- tures except that its internal face is thrown into parallel longitudi- 1893.] NATURAL SCIENCES OP PHILADELPHIA. 99 nal folds, which curve in the direction of the flexure of this part of the intestine which appears to form a loop upon itself. The function of the inter-radial and marginal plexuses of capilla- ries of the young of these fishes, as the accompanying figure shows must be in large measure respiratory. The figure shows the maxi- mum proportional development of the vertical fins, but at a stage about twice the length of the one here figured, the vertical fins begin to become reduced in size so as to approximate their rela- tively reduced proportions in the adult. The integuments of the sides of the body now also become highly vascular, which dermal vascularity also seems to disappear before the birth of the young. The great vascular trunks that especially supply the vertical fins with blood, as shown in the figure, also now atrophy in a measure and become subservient only to the nourishment and metabolism of the tissues of the fins. The histological changes in the fins of these young viviparously developed fishes are therefore very great in the course of their sojourn in the ovary of the parent. That the highly vascular fins and the great vascular trunks which supply them, must in a measure subserve a function in such foetal fishes very sim- ilar to that of a placenta in a non-deciduate foetal mammal, there can scarcely be any doubt. 100 PROCEEDINGS OF THE ACADEMY OF [1898. INVOLUTION FORM OF THE TUBERCLE BACILLUS AND THE EFFECT OF SUBCUTANEOUS INJECTIONS OF ORGANIC SUB- STANCES ON INFLAMMATIONS. By Samuel G. Dixon, M. D. Prof. Robert Koch announced in 1882 the discovery of the cause of Tuberculosis. He claimed that consumption was produced by a peculiar hacillus of a special shape. This he described as a rod- shaped micro-organism with rounded ends, either straight or curved, and frequently beaded. This simple form was accejited as a con- stant character until the summer of 1889, when I first observed, in an artificial culture on an Agar Agar glycerin nidus, a slight incli- nation to bud in one or more places along the rod, without the pro- duction of any particular angle, some relations forming an acute while others formed a right or possibly an obtuse angle. A single bud could only be recognized with a high power objective focused and illuminated with particular nicety. The indications, however, were so often repeated in each field as the slide was moved upon the stage of the microscope that I was sufficiently convinced of the presence of branches to review the life-history of the tube in which they were found and to speculate upon the factors likely to have brought about the evident volution. The result was the production of germs with decided branches, some of which were quite as long as the parent rods or stems. This result was jjublished in the Medical News of October 19th, 1889. In 1891, Prof. Allen J. Smith observed branched forms of tubercle bacilli in human sputum. Since then Prof. Klein, Herren Fischel, Mafucci et al., have described the branching of this germ. In the summer of 1892 I observed the bacillus in this cycle of life in the liver of the Green Jay of Mexico, Xanthoura liixosa. This discovery, coupled with my observations of 1889, and corroborated by the statements of other scientists, must now compel the bacteriological world to recognize a more complex form of the tubercle bacillus than that observed by the great German bacteriologist in 1882. Since the discovery of the branched form of the tubercle germs in 1889, I have been able to continuously reproduce them on artificial mediums. While the young germs seem to be quite simple in form, appearing in straight rods and rods bent upon themselves, those which have arrived at the age of four weeks, particularly in the 1893.] NATURAL SCIENCES OF PHILADELPHIA. 101 presence of an excess of glycerin and in a temperature of 40° C.» become branched. The young bacilli, when introduced into the animal tissues, produce tuberculosis, while the older cultures grad- ually lose their virulence, in all probability owing to their inability to reproduce themselves. This fact indicates that the branched form represents an involution life-cycle of the germ. Notwith- standing the fact, however, that the devitalized, dying or dead ba- cilli cannot produce consumption, they, with their products, effect a decided increase in tubercular inflammation, which inflammatory process even results in necrosis of the tissues. These phenomena led to investigations proving the correctness of the hypothesis first published in my Monograph on Immunity (JNIedical News of Oct. 19, 1889) to wit : " It is possible that, by a thorough filtering out of bacilli from tuberculous material, a filtrate might be obtained and attenuated so that by systematic inoculations a change might be produced on living tissues that would enable them to resist viru- lent tubercle bacilli. In this line of experimentation I proved that the presence of the germs was not necessary to produce the hyper-inflammatory condition of the tuberculous tissue but that it was a product of the bacillus that caused the reaction upon the tuberculous animal tissues. .This, since called Tuberculin and introduced into the human economy for the purpose of curing tuberculosis when introduced into animals suffering with artifi- cially produced tuberculosis, often destroyed the condition called consumption and in many cases appeared to produce immunity to the poison of tuberculosis." The process, however, was not quite so successful in animals Avhich had contracted tuberculosis through one of the natural channels. In these cases, tissues surrounding that which was recognized as tuberculous afterward became infected with consumption. While this was and still is discouraging we have good reason to believe that Tuberculin will be permanently established as a remedy for this pathological condition. The toxic albumose causing inflammation of tissues markedly tuberculous, coupled with the fact that it is found in such tissues, led me to inquire whether or not some other constituents of animal tissues, patho- logical or normal, would produce reaction if introduced in excess into the general circulation. This line of experimentation was begun by first using an albumose of the goat, a comparatively immune animal. This material, however, if at all active as a remedial agent in tuberculosis, is so slow in its effects that I have 102 PROCEEDINGS OF THE ACADEMY OF [1893. heretofore failed to produce any marked changes. When, however, in the course of my investigations I overloaded the animal system with some of its waste products, Dr. William L. Zuill, M. D., D. V. S., who has kindly carried on the clinical work on animals for our Bacteriological Laboratory, reported in the Times and Register of Sept. 26th, 1891, a reaction by the Amide group on inflamma- tory tissues, the animals experimented on being tuberculous. As this group included that which we believe to produce the inflamma- tion of gout, I was led to review my experience with tuberculosis in relation to lithemia. Studying this field with the lithemic and tuberculous habits in view I was soon impressed with the fact that when these diseased conditions were present at the same time in any individual we could claim it to be an exception to the rule. To determine the special action of the Amide group upon inflamed tissues when introduced into the circulation, a case of Lupus vulgaris was selected and first treated by the subcutaneous introduction of .03240 Gm. of Kreatinin, alternated twice weekly with .130 Gm. of Taurin, Urea and Uric acid. The average tem- perature during treatment was slightly raised, though not to any very marked degree, under the influence of such small doses. The more recent patches of Lupus, however, became markedly inflamed, being accompanied with a burning sensation. On the third day after the first injection, a marked granulation could be detected around the outer edge by the aid of a strong amplifying pocket glass. This apparently healthy granulation has continued for ten days, in which time the patch has one half of its original area healed. The result shown at this early stage of the experiment is sufficiently encouraging to warrant not only a continuation of the treatment in this case but in other forms of Tuberculosis. The only other subjects upon which these injections have been tried have been cases of pulmonary tuberculosis in a very advanced stage, where there was too much lung-tissue already destroyed to warrant the expectation of a favorable result. The fact that we apparently have an action on the Lupus and no marked result with small doses on advanced cases of pulmonary tuberculosis causes me to realize that the line of experimentation must not be confined to tuberculous inflammation but extended to the action of these organic substances on the entire group of inflammatory growths, the effect being produced, possibly, by supplying that in which the pathological tissues are deficient. This line of inquiry, which had 1893.] NATURAL SCIENCES OF PHILADELPHIA. 103 its origin in the Bacteriological Laboratory of the Academy, has opened up a new and wide field of important scientific medical investigation. The main object of this communication, at this time, is to confirm the original discovery of the branched form of the tubercle bacillus by recording the observations of the same life- cycle of that micro-organism found in animal tissues. I have, how- ever, ventured to advance theories and results regarding the action of substances far removed from the bacillus, because they were suggested during my studies of the branched form of that organism. 104 PROCEEDINGS OF THE ACADEMY OF [1893. CATALOGUE OF THE CRUSTACEANS IN THE MUSEUM OF THE ACAD- EMY OF NATURAL SCIENCES OF PHILADELPHIA. BY DR. BEXJ. SHARP. According to the catalogue of Professor Lewis R. Gibbes, of Charleston, S. C, published in the Proceedings of the Academy for 1850 (p. 22 to 30), the collection of Crustacea contained one hundred and seventy-five (175) species. In 1851, additions were made by Mr. McAndrews and Messrs E. & C. Wilson. In this year Dr. T. B. Wilson presented the col- lection of Guerin-Meneville, consisting of 413 species (1,482 speci- mens). Thev were classified and catalogued by Dr. R. Bridges, and the collection now contained 980 species (2,054 specimens). In 1852, Edward Wilson, Esq., presented 54 species from Great Britain, and Dr. T. B. Wilson presented 282 species of the Guerin Collection. About 64 species were presented during the year from M. J. Verreaux, of Paris, and Messrs E. Wilson, S. Ashmead, J. Le Conte and others. In 1855, Mr. S. Ashmead presented 34 species. In 1856, 65 species (358 specimens) were received from Messrs W. S. Wilson, S. Ashmead, Davidson and others. In 1857, 15 species were received from Dr. W. Stimpson from the West Coast of America, and 30 species from Drs. W. S. W. Ruschenberger and Hammond and Mr. Pease. In 1858, Mr. W. J. Taylor, Dr, J. L. Le Conte and others, pre- sented 15 species, and Mr. Slack 22 species. In the beginning of the year 1860 the collection contained about 1,000 species. In 1861, the Smithsonian Institution presented 55 species, and G. Davidson 12. In 1864, the Smithsonian Institution presented 62 species, mostly collected by Dr. Wm. Stimpson of the North Pacific Exploring Expedition. In 1872, a collection was presented by Wm. ]\[. Gabb, from San Domingo. In 1873, a fine collection in alcohol from the Fiji Islands was presented by Mr. A. J. Garrett. In 1875, many species were presented by Dr. Wm. H. Jones, of the United States Navy, and during this year the collection was 1893.] NATURAL SCIENCES OF PHILADELPHIA. 1 OS- relabeled and mounted by Messrs C. F. Parker and G. W. Tryon, Jr. Since 1875 but little has been done to the Carcinological Collec- tion of the Academy and many specimens from want of care have been damaged. In 1878, Mr. J. S. Kingsley worked over the Crangonidae and some of the families of the Brachyura, and later Mr. Walter Faxon renamed the Astacidae of the collection. A few species were added to the collection by the Bermuda and Mexican expeditions of the Academy. During the last three or four years Mr. Frederick E. Stearns has added a number of specimens from the Bahamas and West Coast of the United States. In the following catalogue the first number under a species refers to the tray or jar in which the specimen or specimens are placed ;. the second number, in brackets, to the number of specimens cata- logued under the first number : a, meaning alcoholic and d, dried ; thus (2d) means two dried specimens, and (xa) more than ter> alcoholic specimens. STOMATOPODA. SQUILLIDAE Latreille. GONODACTYLUS Latreille, 1825. G. EDWARDsii Berthold, 1847. O. japoniciis DeHaan, 1849. Habitat. Pacific coasts. 23. (Id) China. Dr. T. B. Wilson. 24. (Id) Chili. Dr. T. B. Wilson. G. FALCATUS (Forskael, 1775). Cancer falcatus Forskael, 1775. Squilla chiragra Fabricius, 1793. G. chiragra Latreille, 1825, and authors. Habitat. All seas. 25. (3d) Bahamas. Dr. H. C. Wood, Jr. 26. (Id) Key West, Florida. S. Ashmead. 27. (2d) West Indies. Dr. Morton. 50. (8a) Garden Key, Florida. Smithsonian Institution; 51 & 52. (3a & la). No locality. Smithsonian InstitutioniL 53. (la) Bermuda. Heilprin Collection, 1888. 54. (xa) Tahiti. A. J. Garrett. 57. (5a) Lower California. W. N. Lockington. 111. (3d) Mauritius. Dr. T. B. Wilson. 106 PROCEEDINGS OF THE ACADEMY OP [1893. . LTSIOSQUILLA Dana, 1852. Coronis Latreille, 1825 (name pre-occupied). L. GLABRIU8CULA (Lamarck, 1818). Squilla glabriuscula Lamarck, 1818. Squilla viltata H. Milne-Edwards, 1837. Habitat. Eastern coast of North America. 18. (Id) Key West, Florida. S. Ashmead. 37. (la) Hilton Head, South Carolina. J. J. Craven. 49. (la) No locality. Smithsonian Institution. L. MACULATA (Fabricius, 1793). Squilla maculata Fabricius, 1793. Cancer arenarius Herbst, 1796. Habitat. Indo-Pacific region. 19. (2d) Sandwich Islands. J. K. Townsend. 46. (la) Oahu, Sandwich Islands. Dr. W. H. Jones. L. scABRiCAUDA (Lamarck, 1818). Squilla scabrieauda Lamarck, 1818. Squilla hoeveni Herklots, 1851. L. inornata Dana, 1852. Habitat. Eastern coast of America. 20 & 21. (Id & 2d) Key West, Florida. S. Ashmead. 22. (Id) Brazil. Dr. T. B. Wilson. 44. (2a) No locality. No donor's name. 45. (la) West Indies. Dr. T. B. Wilson. 47. (la) No locality. Dr. T. B. AVilson. PSETJDOSQUILLA Dana, 1852. P. cERisii (Roux, 1828). Squilla eerisii Roux, 1828. Squilla hroadbenti Coco, 1833. Habitat. Mediterranean. 30. (la) Algiers. Guerin Collection. P. ciLiATA (Fabricius, 1793). Squilla ciliata Fabricius, 1793. Squilla stylifera Lamarck, 1818. P. stylifera Dana, 1 852. Squilla quadrispino.^a, Miers, 1880. Habitat. Indo-Pacific region. 15. (5d) Sandwich Islands. Nuttall & Townsend. 16. (Id) Peru. Dr. W. S. W. Ruschenberger. 28. (la) Mauritius. Guerin Collection. 29. (6a) Oahu, Sandwich Islands. Dr. W. H. Jones. 1893.] NATURAL SCIENCKS OF PHILADELPHIA. 107 36. (2a) No locality. Smithsonian Institution. 55. (2a) Tahiti. A. J. Garrett. P. LESSONii (Guerin, 1830), (type No. 4). Squilla cerisii Gueriu, 1830. Squilla lessonii, Guerin, 1830. Squilla spinifrons Owen, 1832. Squilla monoceros H. Milne-Edwards, 1837. P. marmorata Lockington, 1877. Habitat. Indo-Pacific region. 4. (Id) Mauritius. Guerin Collection (Guerin's type). 10, 11 & 12 (Id, la. Id) Chili. Gueriu Collection. 17. (Id) Peru. Dr. W. S. W. Ruschenberger. P. MONODACTYLA (A. Milne-Edwards, 1878.) Squilla monodactyla A. Milne-Edwards, 1878. Habitat. Pacific region. 56. (la) Lat. 6° North ; Long. 166° West. Dr. W. H. Jones. P. STYLiFERA (H. Milue-Edwards, 1837). Gonodadylus sty lifer us H, Milne-Edwards, 1837. Habitat. Pacific region. 13. (Id) Chili. Guerin Collection, 14. (Id) Sandwich Islands. J. K. Townsend. 58, (la) Valpariso, Chili. Dr. W. S. W. Ruschenberger. SQUILLA Fabricius, 1798. including Chlorida Edyoux & Souleyet, 1841 (name pre-occupied). Chloridella Miers, 1880. S. DESMARESTII RisSO, 1816. Habitat. Seas of Europe. 1. (4d) Mediterranean. Guerin Collection. S. DUBiA. H. Milne-Edwards, 1837. S. mantis Desmarest, 1825. S. ruhrolineala Dana, 1852. Habitat. Eastern coast of America. 9. (Id) Trinidad, B. W. I. Dr. Samuel Lewis. S. EMPUSA Say, 1818 (? No. 2 type). Habitat. Atlantic region. 2. (3d) Rhode Island. W. E. Halloway (probably Say's type). 8. (Id) Gulf of Mexico. C.Bryan. 31. (la) New Bedford, Mass. J. H. Thompson. 108 PROCEEDINGS OF THE ACADEMY OF [1893^ 32. (la) No locality. Smithsonian Institution. 33. (la) Hilton Head, South Carolina. J. J. Craven. 34. (la) Beaufort, North ('arolina. E. D. Cope. 35. (la) No locality. J. Walton. 39. ('ia) South America. No donor's name. S. MANTIS Latreille, 1802. Habitat. European Seas. 6. (3d) Mediterranean. Guerin Collection. S. NEPA Latreille, 1825. S. affinis Berthold, 1847. S. oratoria DeHaan, 1849. S. laevis Hess, 1865. Habitat. Indo-Pacific region. 3. (2d) No locality. No donor's name. 7. (3d) China. Dr. T. B. Wilson. 40 & 43. (3a & 2a) No locality. Smithsonian Institution. 41. (2a) Oahu, Sandwich Islands. Dr. W. H. Jones. 42. (la) Malacca. Guerin Collection. S. PRASiNOLiNEATA Dana, 1852. S. dufres7iii Miers, 1880. Habitat. East coast of tropical America. 48. (la) Silam, Yucatan. Mexican Expedition (^(Ze Ives, 1891)^ S. RAPHiDEA Fabricius, 1798. S. mantis var. B major Lamarck, 1818. S. harpax DeHaan, 1849. Habitat. Indo-Pacific region. 5. (Id) India. Guerin Collection. 38. (la) Malacca. Guerin Collection. Numbers 101 to 110 inclusive, are alcoholic specimens of Stoma- topod larvae collected by Dr. W. H. Jones in Central and Eastern Pacific, as far North as Latitude 50°. PENAEIDEA. PENAEIDAE Sp. Bate, 1886. PENAEUS Fabricius, 1798. P. BRASiLiENSis Latreille, 1817. P. brevirostris Kingsley, 1878. Habitat. Atlantic region. 59. (xa) West coast of Florida. Heilprin Collection, 1886 (^de^ Ives, 1891). 1893.] NATURAL SCIENCES OF PHILADELPHIA. 109 60. (2a) St. Martin, D. W. I. Dr. J. van Rijgersma. 63. (5a) San Domingo, West Indies. W. M. Gabb. 64. (2a) Anclote Bay, Florida. Heilprin Collection, 1886 (fide Ives, 1891.) 65. (la) Sand Key, Florida. Heilprin Collection, 1886. 66. (2a) Cat Island, Bahamas. Smithsonian Institution. 69. (3a) Rio Janiero, Brazil. Dr. W. S. W. Ruschenberger. 78. (2a) San Domingo, West Indies. No donor's name. P. BRAsiLiENSis AZTECUs Ives, 1891. (No. 61 types.) Habitat, East coast of Mexico. 61. (xa) Vera Cruz, Mexico. Mexican Expedition, 1890 (Ives* type). 62. (la) Vera Cruz, Mexico. Mexican Expedition, 1890. P. BREVicoRNis H. Milne-Edwards, 1837 (No. 365 type). Habitat. Indo-Pacific region. 365. (Id) Bombay, India. Guerin Collection (H. Milne-Edwards' type). P. cANALicuLATUs (Olivier, 1811). Palaemon canaliculatus Olivier, 1811. P. marginaius Randall, 1839. P.plebejus Hess, 1865. Habitat. Indo-Pacific region and Red Sea. 70. (la) Sandwich Islands. Nuttall & Townsend. 71. (4a) Mauritius. Guerin Collection. P. CRASsicoRNis H. Milne-Edwards, 1837 (? No. 366 type.) Habitat. Indian Region. 366, (Id) Bombay, India. Guerin Collection. P. iNDicus H. Milne-Edwards, 1837. Habitat. Indian region. 77. (la) No locality. Smithsonian Institution. P. KERATHURUS (Forskael, 1775). Cancer kerathurus Forskael, 1775. Palaemon sulcatus Olivier, 1811. P. trisulcatus Leach, 1815. Alpheus caramote Risso, 1816. P. caramote Desmarest 1825, and authors. Habitat. Seas of Europe. 72. (2a) Greece. Dr. T. B, Wilson, 863. (Id) Algiers. Guerin Collection. 110 PROCEEDINGS OF THE ACADEMY OF [1893. P, MEMBRANACEUS RlsSO, 1816. P. longirostris Lucas, 1849 (No. 145, probably type). P. bocagei Johnson, 1863. Habitat. Mediterranean. 145. (la) Algiers. Guerin Collection (? Lucas' type of P. long- irodi-is). P. MONOCEROS Fabricius, 1798. Habitat. Indian region. 360. (Id) Bombay, India. Guerin Collection. P. MONODOv Fabricius, 1798. Habitat. Indo-Pacific region. 74. (la) Mauritius. Guerin Collection. P. SETiFERus (Linnaeus, 1766). Cancer setiferus Linnaeus, 1766. Palaemon setiferus Olivier, 1811. P. orbignyainis Latreille, 1817. P. Jiuviatilis Say, 1817. Habitat. East coast of America. 67. (2a) Hilton Head, South Carolina. J. J. Craven. 68. (2a) New Orleans, Louisiana. Dr. Walker. 75 & 76. (la & 2a) No locality. Smithsonian Institution. 361. (Id) Cuba, West Indies. Gu6rin Collection. 362. (2d) Charleston, South Carolina. Dr. W. Blanding. P. sTYLiROSTRis Stimpson, 1871. P. occidentalis Streets, 1871 (No. 73 type). Habitat. East Coast of Central America. 73. (xa) Panama. McNeil Expedition (Streets' type). P. viLLOSUS Guerin, 1830 (No. 79 type). Habitat. Pacific region. 79. (la) New Ireland. Guerin Collection (Guerin's type). SICYONIA H. Milne-Edwards, 1830. S. SCDLPTA H. Milne-Edwards, 1830. Habitat. Atlantic region and Mediterranean. 100. (la) Hilton Head, South Carolina. J. J. Craven. SERGESTIDAE Sp. Bate, 1886. SERGESTES H. Milne-Edwards 1830. S. ARCTicus Kroeyer, 1855. Habitat. North Atlantic. 112. (la) Lat. 40° 16' 30" North ; Long. 67° 26' 15" West— 828 fathoms. Smithsonian Institution. 1893.] NATURAL SCIENCES OF PHILADELPHIA. Ill EUCYPHIDEA. PASIPHAEIDAE Sp. Bate, 1886. PASIPHaiA Savigny, 1818. P. sivADO (Risso, 1816). Alpheus sivado Risso, 1816. P. savignyi H. Milne-Edwards, 1837. P. brevirostris H. Milne-Edwards, 1837. Habitat. West coast of Europe and Mediterranean, 364. (Id) Nice, France. Guerin Collection. ATYIDAE Kingsley, 1878. ATYA Leach, 1817. Atys Leach, 1815 (name pre-occupied). including Atyoida Randall, 1839. A. BisuLCATA (Randall, 1839) (No. 231 type). Atyoida bisulcata Randall, 1839. Habitat. Sandwich Islands. 162. (xa) Oahu, Sandwich Islands. Dr. W. H. Jones. 231. (Id) Sandwich Islands. T. Nuttall (Randall's type, dam- aged). A. SCABRA Leach, 1815. Habitat. East coast of tropical America. 229. (Id) Mexico. W. Stirapson. 230. (Id) Martinique, Fr. W. I. Guerin Collection. CAEIDINA H. Milne -Edwards, 1837. Caradina Kingsley, 1879. C. AFRiCANA Kingsley, 1882 (No. 163 type). Habitat. Zulu-land, South Africa. 163. (xa) Zulu-land, South Africa. S. A. Grout (Kingsley's types). C. LONGiROSTRis H. Milnc-Edwards, 1837. Habitat. Mediterranean. 233. (Id) Algiers. Guerin Collection. C. TYPUS H. Milne-Ed^vards, 1837. Caradina typus Kingsley, 1879. Habitat. Indo-Pacific Region. 232. (Id) Mauritius. Guerin Collection. 112 PROCEEDINGS OF THE ACADEMY OF [1893. ALPHEIDAE Sp. Bate, 1886. ALOPE White, 1847. A. PALPiPES White, 1847. Habitat. New Zealand and Australia. 234 (Id) New Zealand. Dr. T. B. Wilson. ALPHEUS Fabricius, 1878. including, €ryptophthalmus Rafinesque, 1814. Asphalius Roux, 1831. Dienecia Westwood, 1835. Haplopsyche Saussure, 1857. Alpheoides Paulson, 1880. A. BELLiMANUS Lockington, 1876. Habitat. Coast of California. 118. (3a) San Diego, California. Joseph Jeans. A. BREViROSTRis (Olivier, 1811). Palaemon brevirostris Olivier, 1811. Asphalius brevirostris Roux, 1831. A. malabaricus Hilgendorf, 1878. Habitat. Indo-Pacific region. 245. (3d) Yanaon, French India. Guerin Collection. •246. (Id) Manilla. Dr. Burrough. A. DENTiPES Guerin, 1832 (No. 239 type). Habitat. Mediterranean. 239. (Id) Nice, France. Guerin Collection (Guerin's type). A. DOTO Miers, 1878. Habitat. Australia. 237. (Id) Australia. Dr. T. B. Wilson. A. EDWARDSii Audouin, 1810 (?). ? A. monodon Bosc. 1801. A. pacificus Dana, 1852. A. edivardsii var leviusculus Dana, 1852. A. avariis Sp. Bate, 1887. A. leviusculus (Dana, 1852) Sp. Bate, 1887. Habitat. Tropical seas. 129. (xa) Bermuda. Heilprin Collection, 1888. 135. (la) No locality. W. N. Lockington. 250. (Id) Australia. Dr. T. B. Wilson. A. HETEROCHELES Say, 1818 (? No. 240 type). A.armillatus H. Milne-Edwards, 1837. Haplopsyche lutaria Saussure, 1857. 11893.] NATURAL SCIENCES OF PHILADELPHIA. 113 A. lutaria Saussure, 1858. A. hispinosus Streets, 1872 (No. 134 type). A. equidactijlns Lockington, 1877. Habitat. East coast of America. 133. (2a) Silam, Yucatan. Mexican Expedition, 1890 {fide Ives, 1891). 134. (4a) Panama. McNeill Expedition (Streets' types, A. hispinosus.'). 240. (Id) No locality. Thomas Say (probably Say's type — damaged). 241. (2d) No locality. Smithsonian Institution. 242. (2d) No locality. No donor's name. -A. LAEviGATUs Guerin, 1830 (No. 251 type). Habitat. Pacific region. 251. (5d) Timor. Gueria Collection (Guerin's type — damaged). A. LOTTiNii Guerin, 1830 (No. 249 type)\ A. ventrosus, H. Milne-Edwards, 1837. A. laevis Randall, 1839 (No. 247 type). Aljj/ieoides laevis Kossmann, 1880. Habitat. Indo-Pacific. 115. (xa) No locality (probably from S. Pacific). No donor's name. 131. (2a) ? Japan. Smithsonian Institution. 247. (Id) Sandwich Islands. T. Nuttall (Randall's type of A, laevis). 249. (Id) Mauritius. Guerin Collection (Guerin's type). .A. MALLEATOR Dana, 1852. Habitat. Brazil. 116 & 243. (la & 2d). No locality. Smithsonian Institution. 244. (Id) Brazil. Wilkes' Expedition. A. MEGACHELES (Hailstone, 1835). Hippolyte rubra Westwood, 1835 (not A. ruber H. Milne- Edwards, 1837. Hippolifte megacheles Hailstone, 1835. Dienecia rubra Westwood, 1835. A. edivardsii H. Milne-Edwards, 1837 (not A. edwardsii of Audouin). A. affijiis Guise, 1854. A. milnei Guerin, 1857. A. platyrhynchus Heller, 1862. Cryptophthahnus ruber Costa, 1846. 'See J. S. Kingsley. Bull. Essex. Inst. Vol. XIV. 1882, p. 113. 114 PROCEEDINGS OF THE ACADEMY OF [1893. Habitat. Seas of Europe. 130. (3a) Villa Franca, France. Dr. B. Sharp, 1882. A. MINUS Say, 1818. A.formosus Gibbes, 1851. A. tridentulatns Dana, 1852. A. saulcyi Guerin, 1857 (No. 236 type). A. minor Lockiugton, 1878. Habitat. East coast of America. 117. (xa) Bermuda. Heilprin Collection, 1888. 236. (Id) Martinique. Guerin Collection (Guerin's type, A. saulcyi). 248. (5d) No locality. Smithsonian Institution. 1006. (la) Port Antonio, Jamaica. W. J. Fox. ? A. NOVAE-zELANDiAE Micrs, 1876. Habitat. New Zealand. 252. (2d) New Zealand. No donor's name. A. POEYI Guerin, 1857 (No. 235 type). A. floridianus Kingsley, 1878. Habitat. West Indian region. 235. (Id) Cuba. Guerin Collection (Guerin's type). A. siNuosus Guerin, 1857 (No. 388 type). Habitat. West coast of South America. 388. (Id) Callao, Peru. Guerin Collection (Guerin's type). A. THETIS Miers, 1875. Habitat. Pacific region. 238. (2d) New Zealand. Dr. T. B. Wilson {iide Kingsley, 1882). ATHANAS Leach, 1815. A. NiTESCENs Leach, 1815. Palaemon nitescens Leach, 1815. Arete diocletiana Heller, 1862. Arete nitescens Heller, 1863. Habitat. Seas of Europe. 253. (id) Coast of France. Guerin Collection. PANDALIDAB Sp. Bate, 1886. PANDALTJS Leach, 1815. P. ANNULicoRNis Leach, 1815. p. leavigatus Stimpson, 1854. P. montagui Smith, 1879. Habitat. Circumpolar and North Atlantic. 139. (3a) Lat. 46°, 23' N. ; Long. 52°, 45' W. U. S. Fish Com- mission, 1885. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 115 140. (xa) Massachusetts Bay. U. S. Fish Commission. 141. (xa) Salem, Massachusetts. Dr. T. H. Streets. 142. (4a) Halifax, Nova Scotia. Dr. T. H. Streets. 255. (2d) Belfast Bay, Ireland. W. Thompson (in exchange). P. BOREALis Kroeyer, 1838. Habitat. Circumpolar and North Atlantic. 137. (3a) Salem, Massachusetts, 50 fathoms. Dr. T. H. Streets. 138. (4a) Massachusetts Bay, 40-55 fathoms. U. S. Fish Com- mission. P. DANAE Stimpson, 1854. Habitat. Northwest coast of America. 144. (3a) Marmot Isle, Alaska (45 fathoms). Dr. W. H. Jones. 254. (Id) Coast of Oregon. AV. Stimpson. P. LEPTOCERUS Smith, 1881. Habitat. North Atlantic. 143. (4a) Lat. 41°, 48', 45" N., Long. 65°, 47', 00" W. 85 fathoms; U. S. Fish Commission, 1885. P. PROPiNQuus G. O. Sars, 1869. Habitat, North Atlantic. 136. (2a) Off Martha's Vineyard, 390 fathoms. U. S. Fish Commission. HIPPOLYTIDAE Sp. Bate, 1886. HIPPOLYSMATA Stimpson, 1860. H. WURDEMANNI (Gibbes, 1850). Hippolyte umrdemanni Gibbes, 1850. Habitat. Coasts of Florida. 164. (3a) Pt. Pinellas, Tampa Bay, Florida. Heiiprin Collec- tion, 1886 (fide Ives, 1891). HIPPOLYTE Leach, 1815. H. CRANCHii Leach, 1815. Palaemon viicroramphos Risso, 1816. ff. erasdcornis H. Milne-Edwards, 1837. H. yarelli Thompson, 1853. Habitat. European seas. 258. (2d) Rochelle, France. Guerin Collection. 259. (xd) Pembrokeshire, Wales. E. Wilson. H. FABRicii Kroeyer, 1842. Habitat. North Atlantic. 166. (4a) Salem, Massachusetts. Dr. T. H. Streets. 116 PROCEEDINGS OF THE ACADEMY OF [1893. 167 & 264. (4a & 3d) No locality. Smithsonian Institution. 265. (Id) Coast of Massachusetts. Dr. T, H, Streets. H. GAiMARDii H. Milne-Edwards, 1837. H. gibba Kroeyer, 1842. Habitat. Circumpolar. 150. (la) Lat. 46°, 09', 30" N., Long. 49°, 48', 30" W. 39 fathoms; U. S. Fish Commission, 1885. 155. (4a) Spitzenbergen. Guerin Collection (Guerin mss. type, H. Roberta) . 257. (Id) Maine coast. Dr. J. H. Slack. H. GiBBEROSus H. Milnc-Edwards, 1837. H. gibbosus Dana, 1852. Habitat. Pacific region. 165. (la) Oahu, Sandwich Islands. Dr. W. H. Jones, 1874. 175. (2a) ? South Pacific. No donor's name. H. GROENLANDicA (J. C. Fabricius, 1775). Astacus groenlandica J. C. Fabricius, 1775. Cancer aculeatus O. Fabricius, 1780. Aljyhens aculeatus Sabine, 1821. H. aeuleata Owen, 1835. H. ai-niata Owen, 1839. If. cornuta Owen, 1839. Habitat. Circumpolar. 151. (3a) Marmot Isles, Alaska, 45 fathoms. Dr. W. H. Jones. 152. (la) No locality. No donor's name. 153. (la) Godhaab, Greenland. Dr. Hayes' Expedition. H. LiLLjEBORGii Danielssen, 1861. H. securifrons Norman, 1863. Habitat. North Atlantic. 146. (la) Lat. 42°, 41', 00" N., Long. 64°, 55', 30" W. 62 fathoms ; U. S. Fish Commission, 1885. H. LiNEATA Lockington, 1876. Habitat. Coast of California. 174. (3a) San Diego, California. Joseph Jeans. H. MARMORATA (Olivier, 1811). Palaemon marmoratus Olivier, 1811. Alpheus marmoratus Lamarck, 1818. Habitat. Pacific region. 148. (la) Samoan Islands. J. S. Kingsley (in exchange). 161. (2a) ? South Pacific. No donor's name. 1893.] NATURAL SCIENCES OF PHILADELPHIA. IIT 263. (3d) Sandwich Islands. T. Nuttall. H. MACiLENTA Ktoeyer, 1840. Habitat. North Atlantic. 171. (la) Lat. 47°, 21', 00" N., Long. 51°, 38', 30" W. 81 fathoms r U. S. Fish Commissiou, 1885. 172. (2a) No locality. Dr. T. H. Streets. 256. (3d) Halifax, Nova Scotia. Dr. T. H. Streets. H. PHipPsii Kroeyer, 1840. H. turgida Kroeyer, 1840. H. ochotensis Brandt, 1849. H. vibrans Stimpson, 1871. Habitat. Circumpolar and North Atlantic. 147. (la) Cape Cod, Mass, 90 fathoms. U. S. Fish Commission.. 266. (2d) Salem, Mass. Dr. T. H. Streets. H. POLARIS (Sabine, 1821). Alpheiis polaris Sabine, 1821. Habitat. Circumpolar and North Atlantic. 154. (3a) Salem, Mass. Dr. T. H. Streets. 260. (Id) Arctic Ocean. No donor's name. H. PRiONOTA Stimpson, 1864. Habitat. North Pacific. 393. (2a) Marmot Isles, Alaska, 45 fathoms. Dr. W. H. Jones.- H. PUSiOLA Kroeyer, 1842. Habitat. North Atlantic. 149 & 262. (2a & 4d) No locality. Smithsonian Institution. 261. (Id) Halifax, Nova Scotia. Dr. T. H. Streets. H. TAYLORi Stimpson, ] 857. Habitat. Pacific coast of United States. 173. (3a) Santa Cruz, California. J. S. Kingsley (in exchange)^ LYSMATA Risso, 1826. Melicerta Risso, 1816 (name preoccupied). L. SETiCAUDA (Risso, 1816). Melicerta seticauda Risso, 1816. Habitat. Mediterranean, Japan, Amboina. 271. (2d) Nice, France. Guerin Collection. SPIRONTOCARIS Sp. Bate, 1887. S. SPiNUS (Sowerby, 1806). Cancer sjnnus Sowerby, 1806. 118 PROCEEDIXGS OF THE ACADEMY OF [1893. Alpheiis spiniis Leach, 1815. Hippolyte son-erbaei Leach, 1815. Hippolyte spinu-s Owen, 1835. Habitat. North Atlantic. 156 & 267. (6a & Id) No locality. Smithsonian Institution. 157. (8a) Salem, Mass. Dr. T. H. Streets. 158. (7a) Coast of Maine, Dr. J. H. Slack. 159. (la) Bay of Fundy, 10-20 fathoms. U.S. Fish Commission. 160. (8a) Marmot Isle, Alaska, 45 fathoms. Dr. "NV. H. Jones. VIEBIUS Stimpson, 1860. V. TARiANS (Leach, 1815). Sippolyte varian-s Leach, 1815. Hippolyte smaragdina Kroeyer, 1842. Habitat. European seas. 268. (7d) France. Guerin Collection. V. viRiDis (Otto, 1828). Alpheus viridi-s Otto, 1828. Hippolyte hrullei Guerin (Xo. 269 type). Hippolyte viridi-s H. Milne-Edwards, 1837. Hippolyte m. &Yi.),'\\ith oblong- cylindrical, brownish, 3-septate sporules, 10-12 x S/j.. Anthostomella mammoides E. & E. On dead limbs of Ostrya virginica, London, Canada. June, 1892. (Dearness, No. 1,801.) Perithecia gregarious, about V mm. diam., with thick, coriaceous walls, about half sunk in the inner bark, the upper half raising the closely adherent epidermis into strong, dome-like, hemispherical pustules about 1 mm. across, the prominent, large, papilliform ostiola erumpent. Asci cylindrical, paraphysate, 110-120 x 12-15//, 8-spored, p. sp. 90-110//, long. Sporidia uniseriate, elliptical, brown, 15-22 X 10-13//. 140 PROCEEDINGS OF THE ACADEMY OF [1893. Eutypella amorphae E. & E. On dead stems of Araorpha fruticosa, Rockport, Kansas. Dec, 1892. (Bartholomew, No. 822.) Stromata scattered, numerous and lying close together, but mostly not confluent, conic-convex, about 2 mm. diam., formed above from the scarcely altered but slightly paler substance of the bark, and closely circumscribed by a narrow, black line which does not penetrate the wood. Perithecia 6-8 in a stroma, rather less than I mm. in diameter, globose, with rather thick walls, partly sunk in the surface of the wood, lying closely crowded together, their slender necks rising close together and the rather large subtubercular, sul- cate-clefi, fasciculate ostiola piercing, but not rupturing the closely adherent epidermis, which is not perceptibly raised. Asci clavate, 36-40 X S-Si/j'. (p. sp. 15-20,^ long), 8-spored. Sporidia subbiseri- ate, allantoid, slightly curved, hyaline, with a nucleus in each end, 5-6 xU/'.. Diaporthe albocarnis E. & E. On the smaller dead limbs of Cornus sp, and on Staphylea trifolia and Ostrya virginica, London, Canada. May, 1891. (J. Dear- ness.) Perithecia 2-4 together in a minute, cortical stroma, small {I mm,), solid and white inside, ovate-globose, attenuated above into very short necks with their obscure, scarcely prominent, perforated ostiola united in a flat, black disk, erumpent through the ruptured epidermis which is raised into little pustules thickly scattered over the limbs. Asci clavate, p. sp. about 75 x 7-8//. Paraphyses simple filiform, rather stout, longer than the asci. Sporidia subbiseriate, fusoid 4-nucleate at first, becoming uniseptate (seldom 3-septate) and constricted and slightly swollen on each side of the septum, some- times brownish, 12-20 x 3j-5//. There is no circumscribing line around the stroma but the wood to the depth of about 2 mm. is slightly discolored, presenting a clouded or marbled appearance. The margin of the ruptured epidermis is at first stained yellowish. Sometimes there is only a single perithecium in a stroma. This can hardly be Viaporthe sphingiophora Ouds. On the same limbs occurs Myxosporium niti- dum B. & C, which may be the spermogonial stage. Diaporthe apiospora E. & E. On bark of dead Ulmus, London, Canada. (Dearness), Iowa (Holway.) 1893.] NATURAL SCIENCES OF PHILADELPHIA. 141 Perithecia lying in compact, circinate groups on the surface of the inner bark or slightly buried in it, ovate-globose, black, membrana- ceous, I mm. diam., necks converging with their obtuse smooth ostiola in a small fascicle slightly raising and piercing the thick epidermis, but scarcely rising above it. Asci clavate-cylindrical, 75-80 X 8-10//, pseudoparaphysate, 8-spored. Sporidia obliquely uniseriate or subbiseriate, obovate, 2-celled, the lower cell very small, the upper one much larger and elliptical, each with a single nucleus, hyaline, 11-15 x 6-10,a. This has the habit of Diaporthe with the sporidia of Ajyiospora. Diaporthe ulmicola E. & E. On dead limbs of Ulmus, London, Canada. June, 1892. (Dear- ness. No. 1,869.) Perithecia 8-12 in a pustule, globose, about J mm. diam. slate- color inside, subcircinate, buried in the substance of the inner bark which is unchanged except in being slightly blackened on the sur- face. Ostiola cylindrical, about •' mm. long, erect, straight, rising in close fascicles through cracks in the rough outer bark, often, from the close proximity of the pustules from which they rise, forming an almost continuous series for a centimeter or more. Smooth or some- what quadrisulcate at the apex. Asci (p. sp.) oblong-fusoid, about 40 X 7,"; 8 spored. Sporidia biseriate, oblong-elliptical, 3-4-nucleate , not at all or only slightly constricted in the middle, 8-11 x 3-4/j'.. Diaporthe pruni E. & E. On dead limbs of Prumis virginiana, London, Canada. April, 1892 (Dearness, No. 1,695.) and Iowa (Holway). Stroma cortical, orbicular or elliptical, convex, 3-4 mm. diam., formed from the slightly altered and somewhat paler substance of the bark. Perithecia 8-12, circinate, ovate-globose, 3-5 mm. diam., black, finally subcollapsing, partly sunk in the surface of the wood, contracted above into short necks with their hemispheric-conical ostiola erumpent in a whitish disk which is soon obliterated. Asci clavate-fusoid, 60-65 x 8-10//. (p. sp.). Sporidia biseriate, oblong- fusoid, hyaline, 4-nucleate, slightly constricted in the middle, with a short, cornute appendage at each end, straight, 15-20 x 32-5//.. Differs from Cryptospora pemisylvauica, in its larger, appeudiculate sporidia. The stroma is mostly limited (in the bark) by a black, circumscribing line which, however, does not (usually) penetrate the wood. The appendages are mostly a little bent at the tips ; spores with appendages 18-22// long. 142 PROCEEDINGS OF THE ACADEMY OF [1893. The spermogonia (Cytispm^a pruni Ell. and Dearness), contain an abundance of oblong-fusoid sporules, 2-4-nucleate, hyaline, 10-12 x S/J-. The perithecia appear in the bark, directly beneath the sper- mogonia. Diaporthe calosphaerioides E. & E. On dead stems of Sambucus, London, Canada. April, 1892. (Dearness, No. 1,744.) Stroma cortical, convex, 2-4 ram. diam., raising the bark into broad pustules, sunk to the wood but not penetrating it or sur- rounded by any black circumscribing line, thin, brownish-black, mostly coming off with the bark. Perithecia 6-12, circinate, thin membranaceous and collapsing when dry, about 2 mm. diam., necks slender, decumbent, converging with their brjad-papilliform, finally subumbilicate ostiola joined in a flat, brown disk erurapent through the epidermis and closely surrounded by it. Asci fusoid-clavate, p. sp. 50-60 X 8-10//, with a fugacious stipe 15-20,a. long, and long, lanceolate but very evanescent paraphyses. Sporidia biseriate, allantoid, hyaline, 3-4-nucleate, rounded at the ends, finally uni- septate, about ] 5 x 3-3?//. This has an outward resemblance to Pseudovalsa sambucina Pk., but differs in its sporidia. The long paraphyses and circinate peri- thecia barely covered by the thin stroma indicate a relationship with Culosphceria. Siaporthe aliena E. & E. On Cratcegus (hawthorn), London, Canada. March, 1892* (Dearness, No. 1,793.) Perithecia 4-6 in a pustule, buried in the scarcely altered bark, not sunk in the wood, black, subcom pressed, 2-I mm. diam., with short necks and black, obtuse, coarse ostiola erumpent in a brown, convex disk which is soon obliterated. Asci cylindrical, 75-80 x 7-8/j'.. Sporidia uniseriate, 8 in an ascus, short and obiusely-ellip- tical, hyaline, uniseptate and constricted, with a large nucleus in each cell, 10-13 x l-S.a. According to the specc. of D. crataegi (Curr.) in Cke. F. Brit. ser. 1st, No. 380, this cannot be that species, which in the specc. cited, has smaller perithecia and smaller asci with biseriate, oblong- fusoid sporidia about 15 x Sip-, 4-nucleate, becoming uniseptate. There is some confusion in Currey's figures. The ascus he figures on PI. 48, fig. 135, has uniseriate, elliptical, uniseptate sporidia,. while the sporidia figured at 135 (a), are oblong-cylindrical. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 143^^ Diaportlie spicata E. & E. On dead limbs of Acer spicattim, London, Canada. April, 1892, (Dearness, No. 1,784.) Perithecia few in a pustule (4-8), small (250-300//), black, buried in the bark and not penetrating the wood. Ostiola short- cylindrical or conic-cylindrical, raising the epidermis into little pustules and rupturing or piercing it, but mostly remaining partly covered by it. Asci oblong-fusoid, p. sp. 40 x 7,a. Sporidia biseri- ate, oblong or fusoid-oblong, slightly curved, subacute, about 4- nucleate, becoming 1-septate, hyaline, 12-13 x 3-3?/^. Differ? from D. acerina (Pk.) in its smaller perithecia not sunk ia the wood, and its curved sporidia. Eutypella coryli E. & E. - On dead Cor?//tfs, London, Canada. June, 1892. (Dearness, No^ 1,872.) Perithecia 8-15 in a pustule, globose, coriaceous, about } mm. diam., circinately buried in the unchanged substance of the inner bark, their 4-cleft ostiola erumpent in a convex, black disk 1-2 mm. diam., which is soon obliterated. Asci clavate, 20-30. x 4//, 8-spored. Sporidia biseriate, allantoid, yellowish, moderately curved, 5-6 x The tufts of erumpent ostiola are distinctly prominent. This seems quite distinct from any of the other described species on Coryhis. Fenestella ulmicola E. <& E. On dead limbs of Ulmiis americana, London, Canada. August, 1892. (J. Dearness.) Stroma orbicular, convex, about A cm. diam., closely covered by the epidermis, which is raised into a broad pustule pierced by the minute, black disk but not laciniately torn. Perithecia 6-12, circin- ate in the dull yellowish, light colored substance of the stroma, i-f mm. diam., ovate-globose, their necks converging and their conic- papilliform or convex, black ostiola erumpent and united in the small disk, which rises slightly above the epidermis. Asci cylindri- cal, short-stipitate, paraph y sate ; 110-120x12//. Sporidia uni- seriate, oblong-elliptical, 5-septate, with a longitudinal septum run- ning through, brown, 12-16 x 7-8//. The substance of the stroma is similar to that of i^. vedita, but the asci and sporidia are smaller. 144 PROCEEDINGS OF THE ACADEMY OF [1893. Valsaria staphylina E. & E. On dead limbs of Staphylea trifolia, Loudon, Canada. May, 1892. (Dearness, No. 1.848.) Stromata orbicular or elliptical, 2-3 mm. diam., convex-hemi- spherical, buried in the inner bark which is uniformly blackened on the surface but remains unaltered within, often seriately arranged. Perithecia subcircinate 6-12 in a stroma, 300-350/^. diam., with short, slender necks, the papilliform ostiola erumpent in a small, black, mostly acutely-elliptical disk visible in longitudinal clefts of the slightly raised epidermis. Asci cylindrical, p. sp. 80-90 x 7/j., paraphysate, 8-spored. Sporidia uniseriate, oblong-elliptical, obtuse, dark brown, constricted, 12-15x7-8/^, each cell with a single nucleus. Of less robust growth than V. insHiva not blackening the wood, and only blackening the surface of the inner bark. Diatrypella pulcherrima E. & E. On dead twigs of A^a/ta;, London, Canada. May, 1892. (Dear- ness, No. 1,875.) Stromata minute, gregarious, cortical, raising the smooth epider- mis into convex-hemispherical pustules about 1 mm. diam., and crowned with a minute, white, orbicular disk which is soon obliter- ated in the center by the tips of the crowded, black, smooth, minute ostiola, which do not however rise quite up to the surface of the disk. Perithecia 8-12, minute (1 mm. or less), lying in a subcircin- ate manner in the stroma. Asci (p. sp.) oblong 30-35 x 8-10//., polysporous. Sporidia inordinate, allautoid, hyaline, moderately curved, 8-12 x li/i. H'mnmularia lateritia E. lic E. On bark of dead Fraximis sambiicifolia, London, Canada. March, 1892. (Dearness, No. 1,283.) Stroma carnose-carbonaceous, orbicular, discoid, 2-lcm. across, and about 1 mm. thick, dark reddish-brown, bordered by the mar- gin of the ruptured epidermis, seated on the surface of the inner bark and circumscribed by a black line which penetrates to the ■wood. Ostiola papilliform, becoming umbilicate, scarcely jirom- inent. Perithecia peripherical, ovate 2 mm., or a little more high, and about i mm. broad, forming a closely compacted stratum. Asci clavate, paraphysate, long-stipitate, 100-120 x 8/7., p. sp. 55- j60x8//. Sporidia obliquely uniseriate, navicular, 10-12x4-5/^, 1893.] NATURAL SCIENCES OF PHILADELPHIA. 145 (exceptionally 12-15 x 5-6/j.), nearly hyaline and 2-nucleate at first, becoming opaque and nearly black. Has the habit of Nuni- rmilaria rumpens Ck., but distinguished by its dark red, subcarnose stroma, inconspicuous ostiola and navicular sporidia. * * DISCOMYCETES. Lachnea cervicolor E. & E. On rotten wood, Canada, (Macoun.) Ascomata, suborbicular, sessile, 4-10 cm. diam., flattened (shallow cup-shaped), with the margin entire and incurved when dry ; out- side clothed with a dense coat of short, dark ferruginous hairs, the margin with louger, paler, septate hairs 400-600/^. long and decum- bent or appressed ; disk when dry liver color. Asci cylindrical, 150-200 X 15,a, p. sp. 120-150//, long. Paraphyses abruptly thick- ened at the apex which is about 5//, thick and hyaline. Sporidia uniseriate oblong-elliptical, with one large, oblong nucleus or with two smaller ones, hyaline, 18-22 x 11-12//, epispore smooth or some- limes very faintly granular-roughened. Allied to L. lanuginosa (Bull.), L. hainsei and L. anraiittopsis Ell., but apparently distinct. Orbilia caulophylli E. & E. On dead stems of Caulophjihnn thalietroides, London, Canada. May, 1892. (Dearness, No. 1,825.) Ascomata scattered or gregarious, sessile, gelatinous, pale rose color when fresh, orange when dry, about h mm. diam., disk plane or slightly concave when fresh, more strongly concave when dry, margin thin, spreading and imperfectly laciniate-toothed when fresh, outside clothed with short, pale glandular hairs. Asci clavate-cylin- drical, 40-50 x 5-6//, 8-spored ; paraphyses filiform, not distinctly thickened at the tips. Sporidia biseriate, clavate-oblong, hyaline, continuous, 5-6 x li// (at the thick end.) Helotinm lacteum E. & E. On decorticated wood, Cazenovia, N. Y. Oct., 1887. O. F. Cook, No. 201, and Marcellus, N. Y. Nov., 1889. (Underwood, No. %Q.) Gregarious and subconfluent. Ascomata stipitate, hemispherical, \-\ mm. across, outside and the slightly concave disk with a thin margin, glandular-pruinose, white with a tinge of yellow, the yellow becoming more distinct when dry. Stipe cylindrical, stout, less in length than the diameter of the disk, pale and pruinose. Asci 146 PROCEEDINGS OF THE ACADEMY OF [1893. clavate-cylindrical, 75-80x5//, with a slender stipe-like base* mostly curved, with filiform paraphyses. Sporidia overlappiug uni- seriate or biseriate, fusoid-oblong, curved, becoming 1-3-septate, 10- 15 (exceptionally 20) x 2.i-3,a. This agrees well with the description of H. pallescens, but its smaller size, acutely margined, more distinctly stipitate pruinose cups, and its sporidia often 3-septate seem to separate it from that species. Phialea dearnessii I^. & E. On dead stems of Monarda, London, Canada. May, 1890. (Dear- ness, No. 1,713.) Erumpent, scattered, substipitate, nearly sulphur yellow. Ascom- ata about f mm. diam., subolivaceous at first, becoming yellow, sub- striate, margin subfimbriate, at first incurved then erect, stipe short, less than diameter of the disk, stout. Asci clavate-cylindrical, sub- sessile, 75-80 X 10/j'-, with stout paraphyses scarcely thickened above. Sporidia biseriate, fusoid, slightly curved, with two large nuclei, 30— 35 X 3/i, gradually attenuated to the slender subulate-pointed ends. Chlorosplenium salviicolor E. & E. On dead stems of Vitis vulpina, St. Martinville, La. March, 1889. (Langlois, No. 1,679.) Scattered, subhemispherical at first with the margin incurved, soon expanding to nearly plane, l2-2 mm. across, dark sage-green, pruinose outside contracted below into a short stipitate base. Mar- gin subincurved and subundulate when dry. Asci clavate-cylin- drical, slender, sessile, 30 x 22-3/-'.. Paraphyses branched above and conidiiferous. Sporidia biseriate, oblong, minute, hyaline 3-4 x 1- 1?//.. Smaller throughout and of a duller shade of green than C. ceruginescens Rehm, and does not stain the subjacent wood. Chlorosplenium canadense E. & E. In depressions in the rough bark of Tilia, and on the bare wood, London, Canada. Oct., 1892. (Dearness, No. 2,032.) Ascomata cespitose or solitary, stipitate, 1-2 mm. diam., closed at first, then open and umbilicate or concave, hymenium olive-black, margin grayish and often subrepand orlobed. Stem 2-4 mm. long, olivaceous, roughish under the leus, becoming black, clothed at base with a light-olive tomentum composed of sparingly branched hairs, and finally becoming black. Asci slender clavate, 130-150 x 8-10//, 1893,] NATURAL SCIENCES OF PHILADELPHIA. 147 8-spored, with filiform paraphyses. Sporidia subbiseriate, cylin- drical, nearly straight, multi-nucleate, hyaline, 30-60 x S;j.. Goryne ellUii Berk, Stllhum magnum Pk., is probably the conidial stage. Niptera lithospermi E. & E. On dead stems of Lithospermum canescens, Mount Helena, Mon- tana. Oct., 1889. (Anderson & Kelsey, No. 4.) Erumpent-superficial, scattered, sessile, about I mm. diam., closed at first and opening tardily, black-brown outside and granular from the projecting cells of the external layer, margin whitish. Disk livid white becoming darker, cup-shaped. Asci oblong-cylindrical, sessile, 45-55 x 8-1 O/j-., with obscure paraphyses. Sporidia biseriate, oblong-cylindrical, 1 -septate and mostly broadly constricted in the middle, hyaline, 12-20 (mostly 12-15) x 3-32y. ends, rounded or sometimes obtusely pointed. Hardly distinguishable from Pyreno- peziza nigrella Fckl. outwardly, but the sporidia are very different. MoUisia trametis E. Si, E. Parasitic on Polyporns stevendi Berk. On a decaying oak chip, Newfield, N. J. Dec, 1888. Growing on the margin and .inner surface of the pores. Cups obconic, 114-150// diam. honey colored, of fibrous structure, the ends of the fibers projecting so that the outer surface and the mar- gin appear granulose-pubescent or as if covered with sharp pointed granules, convex-hemispherical at first and imniarginate, so as to resemble Nectria, but soon, becoming concave with a distinct sub- fimbriate margin. Asci clavate-oblong, 20-23 x 4-5,a, sessile and without paraphyses. Sporidia biseriate or obliquely uniseriate, nar- row-elliptical or clavate oblong, hyaline, continuous, 3^-4? x li-2/JL. The cups are so near the color of the pores of the fungus on which they grow as to be easily overlooked. MoUisia nipteroides E. & E. On dead stems of Smila.r, St. Martin ville. La. March, 1889. (Langlois, No. 1,674.) Shallow cup-shaped, 1-1 j mm., across contracted below into a very short stem (almost sessile). Umber color but whitened outside by a pruinose coat and a short erect glandular pubescence which is more abundant toward the margin. Asci oblong-cylindrical, 35-40 X 5-6//, sessile. Paraphyses branched above and bearing minute globose conidia. Sporidia biseriate, hyaline, 2-3-nucleate, oblongs 148 PROCEEDINGS OF THE ACADEMY OF [1893. straight or slightly curved, 4-5 x 11-1?//. More or less contracted with the margin incurved when dry. Dermatea fusispora E. & E. On dead birch limbs, Orono, Maine. (F. L. Harvey.) Ascomata gregarious, obconical, erumpent-superficial, about 1 mm. diam., subolivaceous outside, the subundulate margin and dull reddish disk white-pruinose ; texture loose and soft. Asci narrow- clavate, paraphysate, 70-75 x Q;j.. Sporidia biseriate, fusoid, hyaline, continuous, 15-20 x 2,'j., slightly curved, continuous. Recognized by its reddish disk and fusoid sporidia. Dermatea ohionanthi E. & E. On dead limbs of CMonanthus virginica, Wilmington, Del. May, 1890. (Commons, 1,449.) Sessile, solitary or oftener cespitose in compact fascicles of 2-4, dark chestnut-color, obconic, with a narrow margin, 5-I mm. diam., disk when dry often subrugose, substance firm and dry. Asci 100- 11 0 X 18-20/j'-. Sporidia biseriate, oblong, continuous, obtuse, slightly curved, granular, hyaline or nearly so, 18-22 x T-S/Jt. Dermatella montanensis E. & E. On small, dead limbs, among driftwood, Sheridan, Montana. May, 1892. (Mr. and :Mrs. H. M. Fitch.) Erumpent-superficial, orbicular, discoid immarginate, l-l mm. diam., livid and subgelatinous when fresh, concave and black with a thin erect margin when dry. Asci oblong-obovate, short-stipitate, p. sp. 72-80 X 18-22//, 8-spored. Paraphyses stout, (2-2^// thick), branched and septate, united above in a dark brown epithecium. Sporidia crowded-biseriate, oblong or clavate-oblong, obtuse, 3-septate slightly constricted at the septa, hyaline, becoming yellow-brown, 20-24 X 7-8//. Dermatella caryigena E. & E. On dead limbs of Carya, West Chester, Pa. July, 1889. Cespitose in clusters of 4-8, nearly black, disk slightly convex when fresh, J-l mm. across with a narrow margin. Asci clavate- cylindrical, 75-80 x 10//, with abundant subolivaceous paraphyses slightly thickened above. Sporidia obovate-oblong, subinequilateral, 3-septate, greenish-yellow, 12-14 x 42-6//. The clusters of peri- thecia which are 1-2 mm. across are erumpent through the epider- mis but are attached to it and readily peel off with it. 1893.] NATURAL SCIENCES OF PHILADELPHIA. 149 Dermatella fraxini E. & E. On bark of i^rfmnws, London, Canada. Feb., 1890. (Dearness, No. 1,454.) Gregarious and subcespitose, flesh colored, convex, immarginate f-1 mm. diam., contracted below and slightly obconic. Asci clavate- cylindrical, 125-150 x 12-1 5,a. Sporidia subbiseriate, oblong-cylin- drical, subhyaline and uniseptate at first, then brown and 3-5- septate, 25-35 x 10-12/i. Dermatella hamamelidis E. & E, On dead stems of Hamamelis virginiana, West Chester, Pa. June, 1889. Subcespitose, subsessile, about h. mm. diam., convex becoming concave, immarginate, dark reddish-brown, Asci clavate-cylin- drical, narrowed below into a stout substipitate base, 75-80x12- 15,a, with linear paraphyses. Sporidia biseriate, oblong, subinequi- lateral, yellowish, crowded with nuclei, 12-15 x 5-6,a. Some of the sporidia were faintly, 3-septate and it is probable that at maturity they all become so. In the same locality and at the same time were found specimens of D. purpurescens (on dead chestnut limbs as before) with the sporidia distinctly 3-septate. Cenangella violacea E. & E. On an old cottonwood board, Rockport, Kansas. Dec, 1892. (Bartholomew, No. 833.) Ascomata gregarious, slaty black, sessile with a thick but narrow base, about J mm. diam., disk convex when fresh and deeply rugose, with a narrow obtuse margin, when dry hysteriiform from the rolling together of the opposite sides. Asci obovate, sessile, 35-50 x 15-20,u, 8-spored. Sporidia inordinate, obovate, hyaline, uniseptate and con- stricted at the septum, obtuse at the ends, variable in size 12-20 x 5-10//, almost exactly the same as those of Glonium llneare. Para- physes stout, jointed, swollen above and violet color (under the microscope), bearing hyaline elliptical, continuous conidia, 5-7 x 3-4,a. Belonidiam tympanoides E. & E. On rotten wood, London, Canada. Sept., 1889. (Dearness, No. 948.) Gregarious, carnose, sessile, black and closed when dry, hemis- pherical when fresh and i-i mm. diam., disk concave, pallid, with a 150 PROCEEDINGS OF THE ACADEMY OF [1893. narrow, obtuse margin. Asci clavate-cylindrical, 80-100 xl2,a, with filiform paraphyses curved at the tips. Sporidia cylindrical, hyaline, multiseptate nearly straight, 40-60 x 2ia. The perithecia are at first nearly globose but as the hymenium develops they become excavated above and finally concave. Blitrydium sabalidis E. & E.^ On partly living leaves of Sabal palmetto, Bayou Chene. La. Oct., 1888. (Langlois, No. 1,772.) Perithecia scattered or gregarious, black, conical and closed at first, then open exposing the smoky-gray disk which becomes dirty white, margin sublacerate toothed and subincurved, about 1 mm. diam. All the upper part finally falls away leaving only a black circle with a white center. Asci clavate, 40-50 x 15-20//. Para- physes none ? Sporidia crowded brownish-yellow, oblong, 4-septate with the next to the upper cell divided by a longitudinal septum, 15-20 X 6-7 p.. This is very distinct from Dermatea sabalidis E. & M. ( Cenangium sabalidis in Sacc. Syll. vol. VIII, p. 562.) Diplonaevia melaleuca E. & E. On decorticated Poplar, Sand Coulee, Montana. Oct., 1889. (F. W. Anderson, No. 645.) Perithecia at first closed and buried in the wood, about 1 mm. diam. carnose-membranaceous, thin and black, soon partly erumpent with a round opening at the apex, the margin narrowly white lacer- ate-fimbriate. Disk livid, concave. Asci subcylindrical, subsessile, 75-85 X 6-8,'Ji, surrounded by abundant filiform paraphyses slightly longer than the asci, their tips bent or curved but not distinctly thickened. Sporidia 6-8 in an ascus, biseriate, cylindrical, hyaline, curved, obtuse, 1-septate, 12-15 x 3//. Stictis schizoxyloides E. . BigelovicB, E. k E., N. A. F. 2,248.) On leaves of Gutierrezia euthamia, Digway, Utah. June, 1892. (M. E. Jones, No. 23.) 1893.] NATURAL SCIENCES OF PHILADELPHIA. 155 III. Sori amphigenous, 5-I mm. diam., slaty black, hemispherical^ erumpent and soon naked, crowded or confluent, often surrounding and deforming the leaf. Teleutospores oblong, rather palp, brown, constricted, the upper cell mostly narrowed into a bluntly pointed apex, the lower cell rounded at base or narrowed into the stout, slightly colored pedicel, which is 75-100/-t long. Epispore smooth, thickened at the apex. Fucoinia ludibunda E. & E. On leaves of Car ex sparganioides, Rockport, Kansas. Oct., 1892. (Bartholomew, No. 764.) III. Sori epiphyllous, dark chestnut-brown or nearh^ black, soon naked and prominent, l-3xf-lj mm. Teleutospores clavate or cliivate-elliptical, 40-55 x 12-16/v., constricted at the septum, upper cell more deeply colored and subelliptical, lower cell mostly nar- rower and paler, epispore smooth, distinctly thickened at the apex which is either regularly rounded or prolonged and obtusely pointed or sometimes truncate and in this case, occasionally crowned with 2-3 short horn-like processes as in P. coronata. Pedicel hyaline^ stout, about as long as the spore. Besides the uuiseptate spores, quite an appreciable number of spores are found with two septa. Puccinia tuberculans E. & E. On leaves of ^p/oj9app»s, Muncy, Nevada. July, 1891. (M. E. Jones, No. 21.) III. Amphigenous. Sori scattered or confluent, about 1 mm. diam., covered by the thick epidermis which is raised into rather flat tubercles and finally ruptured, color dark chestnut. Teleuto- spores elliptical or oblong-elliptical, 25-40 x 18-22,^, slightly con- stricted, epispore smooth, light chestnut-brown, thickened at the- apex of the spore and generally raised into a subacute papilla.- Pedicels hyaline, 40-60,^ long. Seems to be a well marked species on account of the tuberculiforna: sori. Puccinia columbiensis E. & E. On (Etiotliera biennis, Banfi*, British Columbia. July, 1891. (J. Macoun.) III. Amphigenous, on yellowish, slightly thickened spots. Sori minute, not over \ mm. diam., nearly black, erumpent, subconcentric- ally arranged and crowded in dense, orbicular patches 1 2-4 mm. across and whitened by the fragments of the ruptured epidermis. 11 154 PROCEEDINGS OF THE ACADEMY OF [1893. Teleutospores clavate, 40-50x18-20/^-, constricted at the septum, upper cell broader and darker, lower cell, attenuated below and paler (subhyaline), epispore smooth, strongly thickened at the rounded or subacute apex. Pedicels as long as or a little longer than the spores. Very distinct from P. ceyiotherce Vize. Puccinia virgata E, & E. On dead leaves of Panicum virgahim, Rockport, Kansas. March, 1892. (E. Bartholomew, No. 496.) III. Sori amphigenous but more fully developed on the lower side of the leaf, linear, often 1 cm. or more long, erumpent and margined laterally by the ruptured epidermis, dark chestnut-brown, almost black. Teleutospores mostly wedge-shaped or clavate but also, some of them oblong, 40-70 x 18-22//, the upper cell shorter and elliptical or subglobose and dark, the lower cell longer, narrower and lighter colored, apex rounded and obtuse or subtruncate, and sometimes a little roughened. Epispore thickened at the apex but without any distinct papilla. Has a general resemblance to P. graminis but the spores are different. Fuocinia lygodesmiae E. & E. (P. variolans Hark? var. caulicola in Ell. and Ev., N. A. F. 2,237.) (I.) ? and III. On stenis of Lygodesmia juiicea, Cheyenne Wells, Colorado. July, 1887. (C. H. Demetrio.) III. Sori about ^ or f mm. diam., densely cespitose in elongated patches partly or entirely surrounding the stems, and sometimes covered by the whitened cuticle, but finally bare and dark chestnut color. Teleutospores oblong-elliptical, constricted at the septum, mostly rounded at each end, epispore smooth, thickened at the apex and often with a broad, sometimes oblique papilla, 35-45 x 20-23//, on stout, persistent pedicels, 100-120// long. The mode of growth is similar to that of P. enormis Fckl., the stems being more or less swollen where occupied by the clusters of sori. This is very distinct from P. harknessii Vize (on Lygodesmia spinosa) but closely allied to P. variolans Harkness, from which, however, it differs in habit and in the epispore being much thinner in the middle of the spore. An jEcidium which may belong here, was found on the same host in Montana, by Mr. Anderson. The secidia arising from yellow 1893.] NATURAL SCIENCES OF PHILADELPHIA, 155 swellings on the stems and leaves, are about J or f mm. high, erect and deeply fimbriate-laeerate above, the membrane thin and white. Aecidiospores, globose, oblong or irregular in shape, smooth or nearly so, 18-22,'j. in the longer diameter. Uromyces macounianus E. & E, On Euphorbia sp. (E. maculata affinis), Vancouver Island, British Columbia. Aug., 1887. (Macoun, No. 322.) II. III. Sori amphigenous, convex or subhemispherical, surrounded by the ruptured epidermis, mostly crowded, light chestnut color, becoming darker, about 1 mm. diam. Uredospores globose or ovate, echinulate, about 15// diam. Teleutospores globose or ovate- elliptical, pale brown, slightly tuberculo-echinulate especially at the apex which is not thickened and is mostly without any distinct papilla, 14-16,a diam. Pedicels shorter than the spores, hyaline and deciduous. Differs from U. euphorbia C. & P., in its smaller, less distinctly roughened spores and crowded, lighter colored sori which often nearly cover one or both sides of the leaf but are not confluent. Uromyces sporoboli E. & E. On Sporobohis asper Rockport, Kansas. Sept., 1892. (Bartholo- mew, No. 783.) III. Sori mostly hypophyllous, black or nearly so, elongated or linear, 1-4 mm. long, soon naked. Teleutospores of variable shape, subglobose, about 20,«. diam., or obovate, 25-30 x 20-22//, or elon- gated-piriform or oblong, 30-40x20-22//, evenly rounded at the apex or oftener with a distinct papilla, epispore smooth, distinctly thickened at the apex, chestnut-brown ; pedicels 70-100// long mostly colored. Differs from U. dactylidis Otth. U. peckianus Fa,r\o\y smd JJ. gram- inicola Burrill in its more robust growth and larger spores, and from the two first mentioned in the absence of paraph yses. ^cidium ludwigiae E. & E. On leaves of lAidivigia sphcerocarpa, Ellendale, Sussex Co., Del, Sept., 1892. (Commons, No. 1,983.) Spots amphigenous, purplish-red above, more obscure below, scattered or subconfluent, suborbicular, 1-3 mm. diam. Aecidia amphigenous, but more abundant below, either standing singly or oftener collected in a compact cluster forming a little tubercle 1-2 mm, diam., as in JSj. myricatum Schw. ; single cups minute (i mm.), 156 PROCEEDINGS OF THE ACADEMY OF [1893. margin sublacerate-toothed, erect or nearly so, component cells sub- quadrate or pentagonal, about 15/j- diam., the marginal ones more elongated (20/./.). Spores orange-yellow, subglobose or subangular,. 12-15//- diam. Berkeley in Grevillea, reports u^eid. epilobii on Ludidgia, but the Delaware specc. on account of their smaller clustered cups and smaller spores, can not be referred to that species. Cerebella spartinae E.