PROCEEDINGS OF THE California Academy of Sciences FOURTH SERIES Vol. XIX SAN FRANCISCO Published by the Academy 1930-1931 COMMITTEE ON PUBLICATION Dr. William E. Ritter, Chairman Dr. C. E. Grunsky J'^Y Dr. F. iM. MacFarland CONTENTS OF VOLUME XIX Pages No. 1. Strong, A. M., and Hanna, G. D. Marine Mollusca of Guadalupe Island, Mexico. Published June 4, 1930. . . . 1-6 No. 2. Strong, A. M., and Hanna, G. D. Marine Mollusca of the Revillagigedo Islands, Mexico. Published June 4-, 1930. 7-12 No. 3. Strong, A. M., and Hanna, G. D. Marine Mollusca of the Tres Marias Islands, Mexico. Published June 4, 1930. . 13-22 No. 4. Baker, Fred, Hanna, G. D., and Strong, A. M. Some Rissoid Mollusca from the Gulf of California. (Plate 1, 4 Text figures). Published July 15, 1930 23-40 No. 5. Baker, Fred, Hanna, G. D., and Strong, A. M. Some Mollusca of the Family Epitoniidae from the Gulf of Cali- fornia. (Plates 2, 3). Published July 15, 1930 41-56 No. 6. Woodring, W. P. Pliocene Deposits north of Simi Valley, California. Published July 15, 1930 57-64 No. 7. Hanna, G. Dallas. Geology of Sharktooth Hill, Kern County, California. (3 Text figures). Published July 15, 1930 65-83 No. 8. Wetmore, Alexander. Fossil Bird Remains from the Temblor Formation near Bakersfield, California. (7 Text figures). Published July 15, 1930 85-93 No. 9. Myers, George Sprague. The Killifish of San Ignacio and the Stickleback of San Ramon, Lower California. (1 Text figure). Published July 15, 1930 95-104 No. 10. Slevin, Joseph R. Contributions to Oriental Herpetology. IV. Hokushu or Yezo. Published July 15, 1930 105-108 No. 11. Setchell, William Albert, and Gardner, Nathaniel Lyon. Marine Algae of the Revillagigedo Islands Expedi- tion in 1925. (Plates 4-15). Published December 30, 1930 109-215 No. 12. Kellogg, Remington. Pelagic Mammals from the Temblor Formation of the Kern River Region, California. (134 Text figures). Published January- 30. 1931 217-397 No. 13. Grunsky, C. E. Report of the President of the Academy for the Year 1930. Published May 29, 1931 399-410 No. 14. Evermann, Barton Warren. Report of the Director of the Museum and of the Aquarium for the Year 1930. Pub- lished May 29, 1931 411-475 Bradley, F. W. Report of the Treasurer of the Academy for the Year 1930. Published May 29, 1931 476-482 Index. Published May 16, 1938 483-496 49767 PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES Fourth Series Vol. XIX, No. 1, pp. 1-6 June 4, 1930 MARINE MOLLUSCA OF GUADALUPE ISLAND, MEXICO^ BY A. M. STRONG AND G. D. HANNA While weathering a storm in tlie shelter of Guadalupe Island on April 20, 1925, the members of the expedition of the California Academy of Sciences to the Revillagigedo Islands made such use of their time as the conditions would permit. Among other activities some dredging was done in the semi-sheltered cove at the south end of the island. The work was done chiefly by G. D. Hanna, E. K. Jordan, and J. R. Slevin.- After some search a small patch of sandy bot- tom was located and by dragging back and forth across this area several times, a fair sample was secured. As might be 'Editor's Note. Since 1921 the California Academy of Sciences has sent three expeditions to various west Mexican localities, and a considerable number of reports has been issued and numbered serially under each. The three series have the following headings: Expedition to the Gulf of California in 1921; Expedition to Guadalupe Island in 1922; and Expedition to the Revillagigedo Islands in 1925. Since it is impossible to foresee when the final papers may be expected from these expeditions, it has been decided to discontinue the use of the headings and serial numbers. As succeeding papers are received they will be issued in the regular publications of the Academy, with sufficient explanation, however, to indicate which of the expeditions con- cerned contributed the material upon which the work is based. In accordance with this plan the present contribution is a direct result of the Expedition to the Revillagigedo Islands in 1925, although a minor amount of data from the Expedition to Guadalupe Island in 1922 is incor- porated.— Barton Warren Evermann, Editor. "See Hanna, Proc. Calif. Acad. Sci., ser. 4, vol. 15, no. 1, pp. 1-113, pis. 1-10, 7 text figs., March 30, 1926, for a general account of the expedition. June 4. 1930 2 CALIFORXIA ACADEMY OF SCIEIVCES [Proc. 4th Ser. expected on such bold shores, much of the sample consisted of volcanic sand and pebbles, worn fragments of shells and other detritus. However, there was a considerable number of species of mollusca, either living or excellently preserved. These are enumerated in the present list which is believed to be justified by the meager knowledge we have heretofore pos- sessed as to the marine life of this remarkable island. In addi- tion, we have included a few other species collected on the shores of the island in 1922 and 1925. Much has been written about Guadalupe, particularly in relation to the vertebrate fauna and the flora.^ The island is surrounded by water approximately 2000 fathoms in depth and is entirely volcanic, although no activity has been recorded in modern times. The surface indicates that the present form is geologically not very old. Nevertheless, many of the birds, insects, land shells and plants have been isolated so long that they have become specifically differentiated from their nearest congeners. They form a typical waif fauna and flora. No definite evidence has been brought forward to indicate that the island has ever been connected, or nearly connected, to the mainland. It is situated about 180 miles south-southwest of San Diego, California. Not much is known of the marine life of Guadalupe other than the seals, sea lions and sea elephants. There are scattered references to the fishes and crustaceans in the literature, and probably the same is true of the algcie. The known mollusca of the island, as represented by the Academy's collection, consists of 87 species, of which nine appear to be undescribed and 24 were previously known only from a few localities in southern California or the northern portion of the coast of Lower California. Twenty-four species show a considerable extension of the known ranges, 22 not having previously been reported south of San Diego or the Coronado Islands, and two not having previously been 'For references to the principal literature, see Hanna, Proc. Calif. Acad. Sci., ser. 4, vol. 14, no. 2, pp. 217-275, pis. 15-19, 2 text figs., Sept.mber 5, 1925. An account of the land shells has been published by H. A. Pilsbry, op. cit., vol. 16, no. 7, pp. 159-203, pis. 6-12, 3 te.'tt figs., April 22, 1927. Vol. XIX] STRONG & HANNA—MOLLUSCA OF GUADALUPE ISLAND 3 reported north of the Gulf of Cahfornia. Sixteen of the species are known to have a wide range extending from ]\Ion- terey or further north to the Gulf of California or further south. Of the 40 species known to reach as far north as Monterey only 16 are reported from the Gulf of California, while of the 23 species which include the Gulf of California in their known range, 20 are known to reach as far north as Catalina Island and 10 as far north as Puget Sound. The fauna, as represented by the collection, is very similar to that of Catalina Island and the Coronado Islands since all but four of the known species have been reported from those localities. The species in the collection are almost entirely shore or shallow water forms which either live on marine algae or on or among the rocks to which kelp is attached. Floating masses of kelp are always present along the southern California coast and the presence of most of the species on the shores of Guadalupe Island can be accounted for most satisfactorily by the supposition that the spawn or fry has been transported by this means. This indicates a current at some time running southerly along the southern California coast and turning out to sea at an angle which carried it past Guadalupe Island. The almost complete absence of species which are characteristic of the Gulf of California or the coast of the southern portion of Lower California, indicates that there has been no similar current from the south since the time when the shores of Guadalupe Island were first able to support marine life. It is well recognized that the fauna of the coast of southern Cali- fornia and the neighborhood islands, containing over 1000 species, is distinctly southern in its affiliations with many species at the extreme northern end of their geographic range. This fact, taken in connection with the indicated current drift to the south, offers some proof that the prevailing ocean cur- rents and climatic conditions along the southern California coast have changed but little during recent geological times. »f»<>-"«*p' 4 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. LIST OF SPECIES FOUND ON GUADALUPE ISLAND 1. Acmcea digitalis Escholtz; Alaska to San Digo. 2. Acmcea paleacea Carpenter; Trinidad to Lower California. 3. Acmaa persona Escholtz; Aleutians to Soccoro Island. 4. Acteocina angusHor Baker & Hanna; Gulf of California. 5. ^sopus arestus Dall; Magdalena Bay. 6. Alaba jeaneltce. Bartsch; San Pedro to Gulf of California. 7. Alabina sp. 8. Alvania aquisculpta Keep; Catalina to Todos Santos Bay. 9. Alvania cosmia Bartsch; San Pedro to San Martin Island. 10. Alvania oldroydcB Bartsch; San Pedro to Coronado Island. This species is present in large numbers. IL Alvania purpurea Dall; Monterey to San Martin Island. 12. Amphithalamus inclusus Carpenter; Monterey to San Martin Island. 13. Amphithalamus tenuis Bartsch; Monterey to Magdalena Bay. 14. Anachis subturrita Carpenter; San Pedro to Todos Santos Bay. 15. Area solida Broderip & Sowerby; San Pedro to Peru. This rock loving species is represented by a single valve and belongs to the dwarfed form of the southern California coast. 16. Astrcea undosus Wood; San Pedro to Cedros Island. 17. Barleeia calif arnica Bartsch; San Pedro to Abreojos Point. 18. Bittium interfossa Carpenter; Monterey to San Diego. 19. Bursa californica Hinds; Monterey to Cedros Island. 20. Ccecum californicum Dall; Monterey to Lower California. 21. Cadulus fusiformis Pilsbrj' & Sharp; Monterey to Cape San Lucas. 22. Calliostoma splendens Carpenter; Monterey to San Diego. 23. Capulus californicus Dall; San Pedro to San Diego. 24. Cerithiopsis sp. 25. Cerithiopsis oxys Bartsch; San Pedro to Abreojos Point. 26. Chama pellucida Sowerby; Oregon to Chile. 27. Circulus rossellinus Dall; San Diego. 28. Crenella divaricata d'Orbigny; Santa Barbara Islands to Panama. This species was described from Cuba. Numerous valves and a few pairs seem to be the same as the west coast form said by Dall to be identical. 29. Crepidula lingulata Gould; Bering Sea to Panama. 30. Cysticus politulus Dall; Santa Barbara to Cape San Lucas. 31. CyprcBolina pyriformis Carpenter; Sitka to Mazatlan. 32. Diastema sp. 33. Fartulum hemphilli Bartsch; San Pedro to Abreojos Point. 34. Fissurella volcano Reeve; Crescent City to Panama. Vol. XIX] STRONG & HANNA—MOLLUSCA OF GUADALUPE ISLAND 5 35. Glycymeris sp. 36. Crippina calif ornica Dall ; San Diego. This species, previously known from the type locality only, is represented by a dozen pairs and several odd valves. 37. Haliotis californiensis Steams; Santa Barbara to Guadalupe Island. 38. Haliotis corrugata Gray; Monterey to San Quentin Bay. 39. Haliotis cracherodii Leach; Coos Bay to Santa Rosalia. 40. Haliotis fulgens Philippi; Farallons to Gulf of California. 41. Hipponix antiquatus Linnseus; Crescent City to Panama. 42. Hipponix tumens Carpenter; Crescent City to San Diego. 43. Hyalina calif ornica Tomlin; San Pedro to Puerto Libertad. 44. I selica fenestrata Carpenter; Puget Sound to Gulf of California. 45. Leptothyra paucicostatu Dall; Monterey to Coronado Islands. 46. Lioiia acuticostata Carpenter; Catalina to Magdalena Bay. 47. Liotia cookeana Dall; Coronado Islands to Gulf of California. 48. Littorina planaxis Philippi; Puget Sound to Magdalena Bay. 49. Lottia gigantea Gray; Crescent City to Cedros Island. 50. Macrocallista pannosa Sowerby; Gulf of California to Chile. This species is represented by many valves, mostly young. 51. Mangilia beta Dall; Point Afio Nuevo to Coronado Islands. 52. Margarites acuticostata Carpenter; Bodega Bay to Coronado Islands. 53. Margarites parcipicta Carpenter; Sitka to San Diego. Specimens of this species are the most mmierous in the collection. 54. Marginella jewettii Carpenter; Monterey to San Diego. 55. Melaxia diadema Bartsch; Monterey to Point Loma. 56. Milneria kelseyi Dall; Monterey to Abreojos Point. 57. Nodulus kelseyi Bartsch; San Pedro to South Coronado Island. 58. Norrisia norrisii Sowerby; California to Cedros Island. 59. Odostomia cepynota Dall & Bartsch; San Pedro to Cape San Lucas. This is one of the few abundant species found; about 300 specimens were taken. 60. Odostamia Clementina Dall & Bartsch; San Clemente and Santa Catalina Islands. 61. Odostomia deceptrix Dall & Bartsch; San Hipolito and Abreojos points. 62. Odostomia eucosmia Dall & Bartsch; San Pedro to Abreojos Point. 63. Odostomia navisa Dall & Bartsch; San Pedro to Scammon Lagoon. 64. Odostomia turricula Dall & Bartsch; Monterey to Abreojos Point. 65. Odostomia virginalis Dall & Bartsch; San Pedro to Abreojos Point. 66. Phacoides calif ornica Conrad; Crescent City to San Ignacio. 67. Phasianella pulloidea Carpenter; Puget Sotmd to Gulf of California. 68. Phasianella rubrilineata Strong; San Pedro to Todos Santos Bay. 69. Philobrya setosa Carpenter; Forrester Island to Gulf of California. 5 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. 70. Psephidia cymata Dall; Santa Barbara Island to Gulf of California. This species is the most numerous of the bivalves. 71. Puncturella cooperi Carpenter; Alaska to Santa Rosa Island. 72. Retusa harpa Dall; British Columbia to San Martin Island. 73. ? Rissoella sp. 74. Rissoina sp. 75. Rissoina sp. 76. Rissoina sp. 77. Rissoina calif arnica Bartsch; Catalina to South Coronado Island. 78. Rissoina cleo Bartsch; Catalina to South Coronado Island. 79. Seila montereyensis Bartsch; Monterey to Todos Santos Bay. 80. Siphonodentalium quadrifissatum Carpenter; San Pedro to San Diego. 81. Tegula gallina Forbes; San Francisco to Gulf of California. 82. Tegula regina Steams; San Clemente Island to Gulf of California. 83. Teinosloma invallata Carpenter; Monterey to Gulf of California. 84. Teinosloma supravallata Carpenter; Monterey to Gulf of California. 85. Triphora pedroana Bartsch; San Pedro to South Coronado Island. 86. Vermiculum anellum Morch; Monterey to Todos Santos Bay. 87. Williamia peltoides Carpenter; Catalina to Gulf of California. PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES Fourth Series Vol. XIX, No. 2, pp. 7-12 June 4, 1930 II MARINE MOLLUSCA OF THE REVILLAGIGEDO ISLANDS, MEXICO BY A. M. STRONG AND G. D. HANNA This report properly constitutes a part of the records of the expedition of the California Academy of Sciences of 1925 to various west Mexican islands.^ The collecting of marine mol- lusca was placed in the hands of Eric K. Jordan and G. D. Hanna who had a special request from Dr. W. H. Dall to do the task as thoroughly as possible at Clarion and Socorro islands. It appears that no previous visitors to these little- frequented places had brought back more than a scattering of shells and these were not sufficient to permit the detennination of the relationships of the group. Indeed, Dr. Dall was led to suppose from the few he had seen from Clarion Island' that an Indo- Pacific fauna was dominant there. Stearns^ in 1894 stated that: "Of Socorro, the principal island of the more distant Revillagigedo group, we know but little or nothing. It was visited several years ago by Grayson, the ornithologist. 'For a general account of this expedition, see Proc. Calif. Acad. Sci., ser. 4, vol. 15, no. I, pp. 1-113, pis. 1-10, text figs. 1-7, March 30, 1926. Various technical reports based upon the collections obtained have appeared subsequently. 'Dall & Ochsner, Proc. Calif. Acad. Sci., ser. 4, vol. 17, r.o. 5, 141-18S, June 22, 1929. 'Steams, Proc. U. S. Nat. Mus., vol. 17, 1894, p. 143. June 4, 1930 8 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. The few marine shells that have been brought from there are, as would be supposed, familiar Gulf [of California] forms." The collection enumerated herein came from Socorro and Clarion islands. The smaller San Benedicto and Roca Par- tida were visited but it was found impracticable to secure any shells. The two larger islands are volcanic with extremely steep submarine slopes. Coral grows in some places but sandy beaches are practically wanting. On the south side of Clarion Island there is a broken coral beach with spots of sand off shore where a limited amount of dredging was practicable ; results were rather indifferent. The chart shows a small sand beach near the west end of Socorro Island but rough weather prevented the investigation of it. As a consequence of these physical barriers, collecting had to be confined almost exclu- sively to shallow waters close in shore. A few beach shells were picked up but most of the collection came from between tides or within reach of a bather below low water. A few species, not otherwise collected, were brought up in the dredge from about 30 fathoms on the south side of Clarion Island. The bottom consisted of rounded chunks of coral and coraline algae. Had a good patch of shell sand been found this list would undoubtedly be greatly lengthened. As it is, the list contains the records of 61 species and they do not bear out the suppositions of either Stearns or Dall. Only two species can be said to belong to the Indo-Pacific region. Many of the species are widely distributed along west American shores. Eighteen are known from the southern California coast or islands, and four of these have not previ- ously been recorded from as far south as the Gulf of Cali- fornia. (The Revillagigedos are about 240 miles south of Cape San Lucas.) The remainder, 41 species, would seem more properly to belong with the Galapagos Islands or Pana- manian faunas than with that of the Gulf of California. The nearest places from which lists of shells have heretofore been published are the Tres Marias Islands, 300 miles east northeast, and Cape San Lucas 240 miles north. From the first locality Stearns* recorded 89 species of which 22 were 'n. Maria Magdalena, five valves. If the Pacific shell is considered as distinct from the West Indian it will take the name of A. isocardia Verrill, 1870. 2. Area Jormosa Sowerby. Maria Magdalena, one valve. 3. Area multicostata Sowerby. Maria Madre; very common. 4. Area mulabilis Sowerby. (vS.) Maria Madre, one specimen; Maria Magdalena, five specimens. 5. Area pacifieaSo-Kerhy. Maria Madre, two valves. 6. Area reticulata GmeVm. Maria Madre, three valves. 7. ^ rcc 5o/i-, punctate outer layer Varices faint over whorls, pointed in the sutures Nodiscala Varices strong over entire surface of whorls Cirsotrema Surface with a thin, chalky outer layer Varices partly obsolete ; sutures pitted Dentiscala Surface without a distinct outer layer Spiral sculpture distinct Shell white Varices terminating at basal keel Punctiscala Varices extending to umbilical region Boreoscala Shell yellow or brown Sculpture evenly reticulated Ferminoscala Occasional ribs strongly varicose Pictoscala Spiral sculpture very fine or wanting Axial ribs strong and thick Opalia Shell Without a Basal Disk Spiral sculpture distinct Varices forming a ridged fold bounding the umbilicus . . . Crisposcala Varices rounding into umbilical region Asperiscala Spiral sculpture very fine or wanting Shell distinctly banded with brown Hirtoscala Shell white Shell slender, turrited Nitidiscala Shell short and broad Varices thin and erect Globoscala Varices thick and reflexed Sthenorytis Vol. XIX] BAKER, HANNA &■ STRONG— THE FAMILY EPITONIID.E 43 We have used the term "varix" with full knowledg-e that the axial ribs in the members of the family are not equivalent to true rest stages in some other genera. However, the word has been so generally applied to these structures in con- chological literature that we believe no good purpose would here be served in abandoning it. Very few of the west American species have been adequately illustrated and this omission has added enormously to the labor of identification. In order to correct matters as best we can we have illustrated all of the species identified in the present collection. In many cases the only information the student has available is a very generalized description in which actual diagnostic characters are not mentioned or if mentioned are not emphasized. Naturally, working from such literature, errors may be made which cannot be corrected until type material is consulted, redescribed or illustrated. Of the 12 species treated in the following pages three are believed to be new ; the other nine seem to fall into described species which have not heretofore been illustrated. In using the obscure name Epitoniutn "Bolten" Roding for the genus we have followed current west American usage without, however, subscribing to the propriety or legality of the adoption of Boltenian names in general. Genus Epitonium "Bolten" Roding, 1798 Epitoniutn "Bolten" Roding, Mus. Boltenianum, 1798, p. 91. Subgenus Nodiscala de Boury, 1889 The species from the west coast which are placed in the sub- genus Nodiscala form a distinct group, very different from the remainder of the Epitoniums. Dall'' described the subgenus as follows : "These are small, slender imperforate shells with ill-defined axial nodes or ribs but only one true varix, which is terminal and much thickened. The shells when in good condi- tion have a soft calcareous outer coat which is punctate or minutely sculptured." To this it can be added that the more »Proc. U. S. Nat. Mus. vol. 53, 1917, p. 474. 44 CALIFORNIA ACADEMY OF SCIENCES fPRoc. 4th Ser. or less ill-defined ribs end in prominent points which coronate the sutures. In addition to the species described below the suboenus con- tains the following from the west coast : Epitonintn spoui^i- osum (Carpenter).* described from Monterey with eig'ht undulated ribs; Ep'itoimim vnazatlanicnm (Dall)," described from Mazatlan. with 20 faint ribs ; and Epitonhim nicxicanum (Dall)," from Acapulco, with nine wide ribs. All three are known only from the type localities. 1. Epitonium (Nodiscala) golischi Baker, 1 1 anna >S: Strt)ng, new species Plate 2 , figures 1 , 2 Shell rather large for the subgenus, with the characteristic calcareous outer coat, dull cream-white : nuclear whorls very small, depressed helicoid. about one antl a half, the first nearly smooth, the second showing the faint beginnings of varices, not sharply differentiated from the succeeding turn; post- nuclear whorls about eight, high between the sutures, very moderately and evenly rounded, with ten broad, low^-rounded. slightly retractive varices, obsolete on the lower whorls, more distinct on the upper turns, terminating posteriorly in broad, rounded points coronating the whorls, appressed to the pre- ceding whorls and separated by rather deep depressions extending into the sutures ; interspaces about as wide as the varices on the lower whorls, proportionally wider above; all postnuclear whorls markcfl by very indistinct, low rounded axial riblets. parallel to. and extending over the varices, crossed by equally indistinct spiral cords, both groups being further marked throughout by quite distinct, irregular and irregularly spaced, microscopic vertical riblets crossed by equally fine spiral cords separated by minute, inci.sed. punctate spiral lines, the punctations unequal, generally circular, rather deep, and placed at the intersections of the interspaces of the vertical riblets ; sutures rather deep, obscured by the coronat- ing varices; base rounded above, concave below a basal disk *Proc. Calif. Acad. Sci., ser. 1, vol. 3, 186.S, p. 222. sProc. U. S. Nat. Mus., vol. 34, 1908. p. 250. •Op. cit., p. 251. Vol. XIX] BAKER, HANNA & STRONG— THE FAMILY EPITONUDM 45 defined by an extension of the last suture as a depressed line with a series of broad holes corresponding- to those on the upper sutures and a second series of holes half way from the basal disk to the anterior extremity of the shell; aperture broadly subpyriform, distinctly effuse below ; outer lip rather thin; basal lip and parietal wall heavily calloused. Length. 13 mm. ; diameter, 5.8 mm. Holotypc: No. 4770, Mus. Calif. Acad. Sci., from San Francisco Island, Gulf of California, and a half-grown para- type (No. 4771). from Puerto Escondido, Lower California, both collected by Fred Baker in 192L The holotype is prob- ably not quite mature as it lacks the "much thickened" termi- nal varix noted by DalF as characteristic of the subgenus. Besides other distinguishing criteria, this species differs from all others of the subgenus described from this coast in being much more obese. It is named for the late W. H. Golisch, one of our most enthusiastic west coast conchologists. 2. Epitonium (Nodiscala) retiporosum (Carpenter) Plate 2, figure 3 Opalia rctiporom Carpenter, Siippl. Rep. Brit. Assoc. Adv. Sci., 1864, p. 660 Proc. Calif. Acad. Sci., vol. 3, 1865, p. 222. One immature example was taken at Cape San Lucas. A free translation of Carpenter's description is as follows : ''Shell similar in shape to O. biiUata. but with entirely different sculpture; nuclear whorls ? (decollated) ; normal whorls seven, slightly rounded, sutures impressed ; with about 14 subacute radiating ribs, rounded, not varicose, the continu- ation above the sutures flattened; last whorl with a riblike, irregularly arranged spiral row of tubercles on the periphery ; entire surface reticulate, with the interstices deeply, irregularly punctate, punctures, minute, close; base angulated by a nodulous rib; aperture rounded, lip continuous, varicose, not sinuated; operculum (?) pauci-spiral. Length 7. length of spire 5, diameter 2.5 mm." To this it can be added that the 'Proc. U. S. Nat. Mus., vol. 53, 1917, p. 474. 45 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. ribs end in rounded knobs in the suture, and that the nucleus consists of four well rounded, glassy whorls of which only the last shows signs of sculpture. An adult specimen from Catalina Island has been chosen for illustration. 3. Epitonium (Nodiscala) espiritum Baker, Hanna & Strong, new species Plate 2, figure 4 Shell of moderate size, elongate-conic, everywhere marked by heavy growth lines, milk-white; nuclear whorls decollated; remaining postnuclear whorls seven and a half, strongly exserted, the first three very convex, the rest strongly angulate in the middle, producing a broad, slightly concave, sloping shoulder on the upper half and a flattening of the lower part ; all whorls marked by low, rounded, irregular, irregularly spaced, slightly retractive axial ribs, about fifteen appearing on all whorls, these ribs terminating superiorly on the lower whorls, and indistinctly on the upper, in rounded, appressed tubercles in the deeply impressed sutures, thus rendering the sutures strongly crenulate, and by from 10 to 20 narrow, rounded spiral cords crossing the axial ribs, separated by well defined sulci which are rendered markedly i)unctate by the heavy growth lines ; base rather long, marked by the same sculpture as the preceding whorls; aperture broadly oval with some flattening on the peripheral side, rendered entire bv a heavy continuous callus and showing the external sculpture within. Length, 6 mm. : diameter, 2.3 mm. Holotype: No. 4778, Mus. Calif. Acad. Sci., and two imma- ture paratypes (Nos. 4779. 4780) collected by Fred Baker at Isthmus Bay, Espiritu Santo Island, Gulf of California. A paratype in the Baker collection was taken by Capt. Geo. D. Porter in the "Gulf of CaHfornia." The species differs radically from any other described from this coast. Vol. XIX] BAKER, HANNA & STRONG— THE FAMILY EPITONIWJE 47 Subgenus Dentiscala de Boury, 1886 This subgenus contains those species with a spiral rib bounding- the basal disk; the more or less obsolete ribs coro- nate the suture and have deep pits between them on the tabu- lated shoulder of the whorl. 4. Epitonium (Dentiscala) crenatoides (Carpenter) Plate 2, figure 5 Opalia crenataides Carpenter, Ann. Mag. Nat. Hist., ser. 3, vol. 14, 1864, p. 47. One immature specimen was taken at the West Anchorage. San Jose Island, Gulf of California and one at Cape San Lucas, Lower California. A free translation of Carpenter's description of this sj^ecies is as follows: "Shell white, margin of spire straight, nuclear whorls?, normal whorls six, compact, in close contact; axial ribs 10, nearly obsolete on the spire, strong on the last whorl, broad, not elevated, ascending the spire in close, almost straight lines; suture deeply punctured between the ribs, suture continued as a broad basal keel ; spaces between the ribs deep, particularly in the sutures, showing subobsolete, sub- nodose spiral threads; not umbilicated; base smooth. Length 13.5. length of spire 9.5, diameter 5.75 mm." 5. Epitonium (Dentiscala) crenimarginatum (Dall) Plate 2, figure 6 Dentiscala crenimarginala Dull, Proc. U. vS. Xat. Mus., vol. 5.>, 1917, p. 473. Thirty- three specime"ns were taken at Smith Island, two at Balandra Bay, Carmen Island, three at the West Anchorage. San Jose Island, one at San Marcos Island, three at Georges Island, fourteen at Sal si Puedes Island, three at Isla Partida. all in the Gulf of California ; one at Las Animas Bay and three at San Antonio Point, Lower California. In the original description of Epitonium creniiiiarginatiim it was stated that the species had been confused with Epitonium crenatoides (Carpenter). The latter is a rare and little known 4g CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Gulf shell but the name has been commonly applied to the former species which rang^es as far north as Monterey. Cali- fornia, as shown by the various published lists. Epitonium crcnhnarginotum (Dall) is characterised by having about 12 axial ribs, strong on the spire, obsolete on the last two whorls, the whorls finely spirally striated, the base smooth. Carpenter described under the name of "Opalia { 'icrciia- toides, var. ) insculpta,'*" a Pleistocene fossil from Santa Bar- bara with 13 or 14 ribs, strong on the spire, obsolete on the last whorl, spiral sculpture none. Dall stated of this that it is somewhat intermediate between the two above noted but with- out the fine spiral surface sculpture. As the spiral striations on the living shells is on a surface coating whicli is easily eroded, leaving a smooth underlayer. this character is not of specific value Tt is not improbable that a study of well pre- served material from the Pleistocene will show that visculptiim (Carpenter) and cren'unarginatnui (Dall) are identical. One other species, Epifoniuiii ncsioticum (Dall)," from Catalina Island, California, is placed in the subgenus. It is smaller, with 12 ribs and sharp spiral sculpture. Subgenus Asperiscala de Boury, 1909 This subgenus contains those species without a basal disk in which the surface between the varicose ribs is marked with spiral sculpture. To the single species described by Carpenter, Dall added 13 more from the west coast. Three of these were found in the Academy's material and a single specimen of another seems to represent a new species. 6. Epitonium (Asperiscala) kelseyi Baker, Hanna & Strong, new species Plate 2, figure 7 Shell of medium size, rather obese, with straight sides, shining white ; nuclear whorls about two, high and prominent, the first somewhat eroded, the second showing a minute thim- •Ann. Mag. Nat. Hist., ser. 3, vol. 17, 1866, p. 277. 'Proc. U. S. Xat. Mus., vol. S3, 1017, p. 473. Vol. XIX) BAKER. HAiVNA & STRONG— THE FAMILY EPITONIID.E 49 ble-pitting in spots ; transition to postnuclear sculpture not well defined; postnuclear whorls nearly eight and a half, slopingly shouldered above, strongly and evenly rounded below the shoulder, marked by eighteen thin, slightly reflected, irregular and irregularly placed, varices, which are depressed at the sutures, but raised at the shoulder to rounded tubercles which occasionally become spinose; varices not continuous up the spire which they encircle about ;>4 : interspaces wider than the varices, everywhere marked by irregular and irregularly spaced, incised spiral lines quite generally showing faintly on the varices; postnuclear whorls marked throughout by minute pfrowth lines reaching the anterior surfaces of the varices ; sutures deep and w ell defined between the varices ; base well rounded, without a basal disk; aperture ovate, slightly effuse below ; outer lip somewhat fractured but thin, indicating prob- able immaturity; basal lip and parietal wall with a broad callus reflected above, and free from the ends of the varices in such a manner as scarcely to hide the umbilicus. Length. 11.9 mm. : diameter, 5.5 mm. Holoiypc: No. 4766, Mus. Calif. Acad. Sci., collected by Fred Baker at San Francisco Island, Gulf of California, 1921. This species probably resembles E. imperforatum Dall^" more closely than any other from this coast, but it is larger, has fewer varices, a thimble-pitted nucleus and. apparently, a greater tendency to become spinose at the shoulder, besides being perforate. It appears to us that this last criterion is not of great taxonomic importance in Epifonium because the usual broad callus of the columellar region may easily obscure a quite large umbilicus. However, the very free reflection of the callus in this species makes obscuration very improbable at any stage of growth. We are inclined to agree with DalP^ rather than with de Boury.^- that the number of varies, at least in the '"Ppjc. U. S. Xat. Mu3., vol. .S.5, 1917, p. 476. ""The number of varices is, on the whole, very constant in most of the groups, following the rule that the greatest variation will be found where the normal number of varices is greatest." Proc. U. S. Nat. Mus., vol. 53, 1917, p. 471. '""Bien que le nombre des cotes axiales soit une indication relativement tr6s utile dans nombre de cas, il est souvent si variable, nieme chez les especes a cfites peu nombreuse, qu'il faut n'en tenir compte qu'avec une extreme prudence et ne pas y attacher la meme importance que notre savant coUcguc, qui attribue a ce caractferc une Constance en realite tr&s relative." Jour, de Conch., vol. 64, 1918, p. 34. SO C" 50 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. majority of our west coast species, is generally a dependable criterion. The species is named for Mr. F. W. Kelsey of San Diego, California. 7. Epitonium (Asperiscala) acapulcanum Dall Plate 2, figure 8 Epitonium acapulcanum Dall, Proc. U. S. Nat. Ahis., vol. 53, 1917, p. 475. A single specimen was taken at Isthmus Bay, Espiritu Santo Island, Gulf of California. This species is characterized by Dall as having 11 varices, without spinosity at the shoulder, the whorls covered with closely adjacent flattish threads; the three nuclear and five sub- sequent whorls measuring 5 mm. in length by 2.5 mm. in diam- eter. Our specimen has six whorls and is slightly larger than the type in all dimensions. It seems to agree in most particulars but the varices are slightly less retractive. The number of threads in the intercostal spaces of the penultimate whorl is about twenty. 8. Epitonium (Asperiscala) xantusi Dall Plate 3, figures 1, 2 Epitonium xanlusi Dall, Proc. U. S. Nat. Mus., vol. 53, 1917, p. 475. A single specimen taken at Isthmus Bay, Espiritu Santo Island, Gulf of California, and about two dozen specimens at Cape San Lucas, Lower California, seem to fall here. The species is characterized b}' Dall as having 12 low, con- tinuous varies, not spinose or expanded over the suture, the interspaces on the whorls with flattish adjacent threads; the seven decollated whorls measuring 5.5 mm. in length by 3 mm. in diameter. None of our specimens reach quite the seven whorls of the type and the measurements are proportionally smaller. The nuclear whorls are nearlv three, axiallv rctrac- Vol. XIX] BAKER, HANNA & STRONG— THE FAMILY EPITONIID^ 5 J lively, very minutely striated, the direction agreeing with that of the varices. The intercostal spiral cords number from eight to twelve, nearly equal, equally spaced and very distinctly marked. 9. Epitonium (Asperiscala) cookeanum Dall Plate 3, figure 3 Epitonium cookeanum Dall, Proc. U. S. Nat. Mus., vol. 53, 1917, p. 475. A single beach worn specimen from Isthmus Cove, Espiritu Santo Island, Gulf of California, agrees with Ball's descrip- tion and with a specimen from Ocean Beach, near San Diego, in Dr. Baker's collection. No type locality was designated in the original description but the range was stated to be from San Diego to Gulf of California. Dr. Baker's specimen is marked "co-type" and is believed to have been received from Miss Cooke; it is very probably part of the type lot and has been chosen for figuring here. Subgenus Nitidoscala, de Boury, 1909 This subgenus contains those species without a basal disk in which the surface of the whorls between the varices is without spiral sculpture. The majority of the species from the west coast belong- in this subgenus, the total number being nearly 50. Many of these are only known from type si>ecimens and there has been much confusion in the application of the older names. Only four species falling in the subgenus were found in the Academy's Gulf material. 10. Epitonium (Nitidoscala) apiculatum Dall Plate 3, figures 4, 5, 6 Epitonium apiculatum Dall, Proc. U. S. Nat. Mus., vol. 53, 1917, p. 480. Two specimens were taken at the Salt Works, Carmen Island, two at Amortajada Bay, San Jose Island, one at Isth- mus Bay, Espiritu Santo Island, all in the Gulf of California ; 52 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. three at La Paz, one at San Evaristo Bay and two at Coyote Bay, Conception Bay, Lower California. This species is characterized by Dall as having eight sharp varices, acutely angled at the shoulder and becoming spinose on the last whorl ; the 2^ nuclear and five subsequent whorls measuring A mm. in length by 2 mm. in diameter. The species was evidently described from an immature individual. We figure an immature specimen which agrees very closely with the type-description and another with seven and a half post- nuclear whorls; this last is 9.2 mm. in length and 3.3 mm. in diameter ; the varices are continuous and make nearly a whole turn of the spire. 11. Epitonium (Nitidoscala) propehexagonum Dali Plate 3, figure 7 Epitonium propehexagonum Dall, Proc. U. S. Nat. Mu.s., vol. 5.i, 1017, p. 479 One specimen from Puerto Escondido, Lower California, one from Sal si Puedes Island and one from San Luis Island, Gulf of California, seem to fall here. Dall separated this species from the wider ranging Epi- toniiun hexagonum (Sowerby), the only other species from the west coast with six varices, by the larger size, broader pro- portions and greater tendency to spinosity on the varices at the shoulder of the whorls. Judging from the description alone our specimens possess these characters. 12. Epitonium (Nitidoscala) hexagonum (Sowerby) Plate 3, figure 8 Scala hexagona Sowerby, Proc. Zool. Soc, London, 1844, p. 29. Epitonium hexagonum (Sowerby), Dall, Proc. U. S. Nat. Mus., vol. 53, 1917, p. 479. A single specimen from Isla Danzante, Gulf of California, seems to fall in Sowerby's species as restricted by Dall. Vol. XIX] BAKER, HANNA & STRONG— THE FAMILY EPITONIIDM 53 13. Epitonium (Nitidoscala) colpoicum Dall Plate 3, figure 9 Epitonium colpoicum Dall, Proc. U. S. Nat. Mus., vol. 53, 1917, p. 478. A single specimen from Ballandra Ba3^ Carmen Island, Gulf of California, has one more whorl than the original description calls for and it is accordingly larger. The lack of any indication of coronation to the varices and the "pit-like cavities" in the suture between the varices make this species quite distinct from any other described form. 54 CALIFORNIA ACADEMY OF SCIENCES [Pkoc. 4th Sbr. Plate 2 Fig. 1. Epitonium golischi B. H. & S., n. sp. Holotype No. 4770 (C. A. S.); San Francisco Island, Gulf of California; length 13.0 mm.; diameter 5.8 mm.; p. 44. Fig. 2. Epitonium golischi B. H. & S., n. sp. Paratype No. 4771 (C. A. S.); Puerto Escondido, Gulf of California; length 7.6 mm.; diameter 3.5 mm.; p. 44. Fig. 3. Epitonium retiporosum (Carpenter). Plesiotype No. 4777 (C. A. S.); White's Landing, Catalina Island, California, 30 fms.; length 9.5 mm.; diameter 3.2> mm.; p. 45. Fig. 4. Epitonium espiritum B. H. & S., n. sp. Holotype No. 4778 (C. A. S.); Isthmus Bay, Espiritu Santo Island, Gulf of California; length 6.0 mm.; diameter 2.1 mm.; p. 46. Fig. 5. Epitonium crenatoides (Carpenter). Plesiotype No. 4768 (C. A. S.); west side San Jose Island, Gulf of California; length 9.8 mm.; diameter 4.2 mm.; p. 47. Fig. 6. Epitoniujti crenimarginatum (Dall). Plesiotype No. 4774 (C. A. S.); San Marcos Island, Gulf of California; length 18.8 mm.; dia- meter 7.3 mm.; p. 47. Fig. 7. Epitonium kelseyi B. H. & S., n. sp. Holotype No. 4766 (C. A. S.); San Francisco Island, Gulf of California; length 11.9 mm.; dia- meter 5.5 mm.; p. 48. Fig. 8. EpitoniuTH acapulcanum Dall. Plesiotype No. 4769 (C. A. S.); Isthmus Bay, Espiritu Santo Island, Gulf of California; length 6.2 mm.; diameter 2.9 mm.; p. 50. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 5 BAKER, HANNA & STRONG] Plate 2 » 55 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Skr. Plate 3 Fig. 1. Epitoniiim xavtusi Dall. Plesiotypc No. 4775 (C. A. S.); Isthmus Bay, Espiritu Santo Island, Gulf of California; length 4 mm.; diameter 1.0 mm.; j). 50. Fig. 2. Epitonium xantusi Dall. Plesiotype No. 4776 (C. A. S.); Cape San Lucas, Lower California; length 5.5 mm.; diameter 2.8 mm.; p. 50. Fig. 3. Epitonium cookeanum Dall. Plesiotype in the collection of Dr. Fred Baker; Ocean Beach, San Diego, California; length 7.1 mm.; diameter 3.2 mm.; p. 51. This specimen is probably from the type lot returned by Dr. Dall; it is more important than an ordi- nary plesiotype. Fig. 4. Epitonium apiculatum Dall. Plesiotype No. 4763 (C. A. S.); Salt Works, Carmen Island, Gulf of California; length 9.2 mm.; diameter 3.3 mm.; p. 51. Fig. 5. Epitonium apiculatum Dall. Plesiotype No. 4764 (C. A. S.); La Paz, Lower California; length 3.8 mm.; diameter 1.7 mm.; p. 51. Fig. 6. Epitonium apiculatum Dall. Plesiotype No. 4765 (C. A. S.); Isthmus Bay, Espiritu Santo Island, Gulf of California; length 4 mm.; diameter 1.7 mm.; ]>. 51. Fig. 7. Epitonium propehexagonum Dall. Plesiotype No. 4772 (C. A. S.); Inner Lagoon, San Luis Island, Gulf of CaHfornia; length 18.7 mm.; diameter 7.7 mm.; p. 52. Fig. 8. Epitonium hexagotium (Sowerby). Plesiotype No. 4767 (C. A. S.); Isla Danzante, Gulf of California; length 14.1 mm.; tliameter 5.7 mm.; p. 52. Fig. 0. Epitonium colpoicum Dall. Plesiotype No. 4773 (C. A. S.); Ballandra Bay, Carmen Island, Gulf of California; length 13.2 mm.; dia- meter 6.9 mm.; p. 53. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 5 1 BAKER, HANNA & STRONG ] Plate 3 8 PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES Fourth Series Vol. XIX, No. 6, pp. 57-64 July 15, 1930 VI PLIOCENE DEPOSITS NORTH OF SIMI VALLEY, CALIFORNIA <*-^ BY W. P. WOODRING Batch Graduate School of the Geological Sciences, California Institute of Technology, Pasadena The youngest Tertiary rocks on the south slope of the Santa Susana Mountains north of Simi Valley, in eastern Ventura and western Los Angeles counties, consist of sand- stones and conglomerates that lie unconformably on beds ranging in age from upper Miocene to Eocene. Though they are the youngest consolidated deposits in this region, they embrace rocks that are far harder than any of the other Ter- tiary rocks; they cap high ridges and supply the most dur- able rock waste to the streams. These beds, which are several hundred feet thick in tlie eastern part of the area described and thicken westward, were described by Kew,^ who referred them to the Fernando forma- tion and on the basis of a collection of fossils from "Browns Canyon below the abandoned wells" recognized their Pliocene 'Kew, W. S. W., Structure and oil resources of the Sinii Valley, southern California: U. S. Geol. Survey Bull. 691, pp. 333-334, 1919. July 15, 1930 58 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Ser. age and that they are younger than the Pliocene beds of Els- mere Canyon near Newhall. Later Kew^ referred these de- posits to the Saiigus formation and listed a few fossils from additional localities in this region. These Pliocene beds were examined during the course of work carried on by the 1929 summer field camp of the Cali- fornia Institute of Technology by parties headed by F. D. Bode, J. W. Daly, W. A. Findlay, K. E. Lohman, and G. F. Taylor. Any credit for the additional information discovered belongs to these students and their collaborators, who per- formed the arduous work of mapping and fossil-collecting. Not enough time was spent on this part of the Tertiary sec- tion to yield precise stratigraphic results in the way of measurements and possible subdivisions. These matters are now being investigated by G. H. Anderson, of the California Institute of Technology. The fossils collected during the work of the summer field camp confirm Kew's original age assignment and show that at least the lower part of these beds falls within a division of the Pliocene series that furnishes a readily recognized datum horizon in southern California. The fossils and the localities where they were collected are as follows : *Kew, W. S. W., Geology and oil resources of a part of Los Angeles and Ventura counties California: U. S. Geol. Survey Bull. 753, pp. 69-70, 81-89, 1924. Vol. XIX] WOODRING— PLIOCENE DEPOSITS NORTH OF SIMI VALLEY 59 5 .0 «3 CO o 00 »0 ON vo 10 o X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X O (J d, CM 000000 O O O O O !> pL| Oh Cl, PL, Oi Cm l/J U) t/3 6 S S c3 cd cd 2 2 2 u o o X X X X .2 '55 a < c o CS O w Ol o o i5 U * * ctJ o 2 o W ^ iS C £ G V 3 4) w ■^00 ^ .2 -g O (-1 Ih o +^ p C G tH Ql o 9> .0 o J3 a o BO O O. O X u Q o •o u -♦J •§ .g i (It 2 ■3 eg- 60 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Ser. 00 O m 00 1^ X X XX XX X X X X X X 8 S c3 CO O < to "to X X X A A X X i: vO j •* 1 in 5 a £ c5 1- .s .. ,2 •'^ o ca S g O w C3 Q en 'o o o o .S O rt 2 Q o ns ii PQ e o o g-2 o wi rt i < O U3 * * o E o -4-) o -a O c o "5. w e -4-> a o a •c > 73 >> Q c C3 C 0) 7i o .2? > i 9 .2 S « <« a O c > 2 m C i^ -"S o en 3 'S o 3 3 rt o o fc S 2 2 O < 2 S >. •a a o O. 'Ji Vol. XIX] WOODRING— PLIOCENE DEPOSITS NORTH OF SIMI VALLEY ^\ California Institute of Technology locality numbers 433. East of Aliso Canyon, cliff at end of road near center of sec. 36, T. 3 N., R. 17 W.; 7400 feet N. 58° E. from Rocky Peak. G. F. Taylor. 435. East of Aliso Canyon, south line of sec. 25, T. 3 N., R. 17 W. ; on north- ward-facing cliff in burned-over area, 7650 feet N. 45J^° E-. from Rocky Peak. J. W. Daly. 434. Spur east of Aliso Canyon, western part of sec. 36, T. 3 N., R. 17 W.; 30 feet above fault contact with Eocene, 6800 feet N. 64J^° E. from Roclcj' Peak. J. W. Daly. 457. West of Aliso Canyon, east slope of ridge near center of sec. 26, T. 3 N. R. 17 W., 8800 feet N. 12J^° E. from Rock^ Peak. G. F. Taylor. 436. West side of Las Llajas Canyon, about 100 feet below top of cliff section, 2750 feet N. 68° E. from 2205-Hill. W. A. Findlay and J. Reilly. 440. Same locality as 436, but about 75 feet below top of cliff section. W. A. Findlay and J. Reilly. 445. Same locality as 436, immediately below lowermost conglomerate in cliff section. W. A. Findlay and W. P. Woodring. 437. On ridge between forks of first canyon west of Las Llajas Canyon, 5950 feet N. 273^° E. from 2205-Hill. W. A. Findlay and J. Reilly. 441. East of Dry Canyon, 5500 feet N. 36° W. from 2205-Hill. W. A. Findlay. 446. East of Dry Canyon, 4550 feet N. 36M° W. from 2205-Hill. J. Reilly. 439. East of Dry Canyon, 5200 feet N. 39° W. from 2205-Hill. J. Reilly. 442. East side of Dry Canyon near top of ridge, 7000 feet N. 45° W. from 2205-Hill. W. A. Findlay and J. Reilly. 451. East of Dry Canyon, south slope of 2075-Hill, peak of which is 1650 feet N. 79° W. K. E. Lohman and W. B. Maitland. 447. East of Dr>' Canyon, south slope of 2075-Hill, peak of which is 950 feet S. 54° E. K. E. Lohman and W. B. Alaitland. 438. West side of main branch of Dry Canyon. 2000 feet N. 583^° W. from 2075-Hill. K. E. Lohman and W. B. Maitland. 450. West side of main branch of Dry Can>on, 2100 feet X. 54^° W. from 2075-Hill. K. E. Lohman and W. B. Maitland. 448. Main branch of Tapo Canyon, road cut about 30 feet north of pumping plant, 450 feet S. 40^° W. from 1794-Hill. K. E. Lohman and W. B. Maitland. It is apparent from the preceding list that these fossils rep- resent a warm-water Pliocene fauna, which has been found at localities from Lower California northward to the Ventura Basin and which is best known as the fauna of the San Diego formation. "Pecten" veatchii Gabb, a tropical Nodipccten described from Cedros ("Cerros") Island, Lower California, heretofore has not been recorded so far north. Manv other ^7 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Species in this list are found in the Pliocene deposits of Cedros Island* and at San Diego. So far as I know the only locality around the borders of the Los Angeles Basin where this fauna is found is near the mouth of Temescal Canyon northwest of Santa Monica where the following fossils were collected : Pliocene fossils from Temescal Canyon 55. West side of Temescal Canyon, 200 yards above mouth, massive gray sandstone. H. W. Hoots and W. P, Woodring. Brachiopod: Dallinella occidentalis (Dall) Gastropod : Opalia varicostata Steams Lamellibranchs : Ostrea vespertina Conrad Pecten bellus hemphilli Dall? Pecten steamsii Dall "Pecten" healeyi Arnold "Pecten" cerrosensis Gabb "Pecten" purpuratus Lamarck var. Chlamys hastatus (Sowerby) Chlamys opuntia (Dall) Chlamys swiftii parmeleei (Dall) *Phacoides annulatus (Reeve)? *Miltha cf. xantusi (Dall) ♦Specimens represented by molds. The San Diego affinities of the fossils from this locality were recognized by Arnold.^ The similarity of this small fauna to that found at many localities north of SimiValley is striking, and it is quite clear that the same faunal zone is represented. There are not many Pliocene faunal zones in southern California that can be so definitely recognized at such widely separated localities and the beds constituting this zone should have a uniform stratigraphic nomenclature. The deposits north of Simi Valley certainly should not be called the Saugus formation, at least not until it is conclusively shown that the tyi)e nonmarine Saugus formation grades laterally into this zone. The name Saugus formation has been used as a catch-all for almost any Pliocene and Pleistocene beds in the *See Jordan, E. K., and Hertlein, L. G., Proc. Calif. Acad. Sci., 4th ser., vol. 15, no. 14, 1926, pp. 409-464. 'Arnold, Ralph, New and characteristic species of fossil moUusks from the oil-bearing Ter- tiary formations of Southern California: Proc. U. S. Nat. Mus., vol. 32, p. 527, 1907. Vol. XIX] WOODRING— PLIOCENE DEPOSITS NORTH OF SIMI VALLEY 53 Ventura and Los Ang-eles basins. In the Las Posas Hills, not more than 15 miles southwest of Simi Valley, the so-called Saugus formation consists of a lower part carrying a cool- water upper Pliocene fauna and an upper part carrying a warm-water, presumably interglacial. Pleistocene fauna, according to Pressler's account." For the Pleistocene beds Pressler proposed the name Las Posas formation. As Pressler surmised, the beds referred to the Saugus fonnation north of Simi Valley are older than any part of the Las Posas Hills section. The cross-bedded sands and gravels that are well exposed on the Grimes Canyon road, northwest of Simi Val- ley, probably represent the landward edge of the Las Posas formation.'^ These beds constitute the upper division of the Saugus formation of this region as described by Kew.* By tracing westward from the region north of Simi Valley the beds carrying the fauna of the San Diego formation it should be possible to determine the relations of the Pliocene and Pleistocene parts of the so-called Saugus formation. Beds carrying a San Diego fauna could be given a new name in each basin, which would complicate an already cum- bersome nomenclature; they could be called the San Diego formation regardless of where they are found, just as deposits of Paleocene age in California are referred to the Martinez formation wherever they are found : or a zonal nomenclature could be adopted and they could be referred to as the healeyi- zone (after "Pectcn" healeyi), or by some other fossil name that would instantly bring to mind the San Diego fauna. The latter course seems to be the preferable one, for it would yield a definite meaning. Whether the San Diego formation and equivalent deposits elsewhere are called middle Pliocene or upper Pliocene depends on where the Pliocene-Pleistocene boundary is placed. ¥[. R. Gale and U. S. Grant IV, of Stan- ford University, who are completing a study of the Pliocene and Pleistocene of southern California, consider these deposits middle Pliocene. The fossils collected north of Simi Valley and in Temescal Canyon represent only a small fraction of the fauna living •Pressler, E. D., The Fernando group in the Las Posas-South Mountain District, Ventura County, California: Univ. Calif. Bull. Dept. Geol. Sci.. vol. 18, No. 13, pp. 325-345, 4 figs.. 1929. 'Idem, p. 344. »U. S. Geol. Survey Bull. 753, p. 85, 1924. ^ CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. when tliese beds were laid down and the question arises as to the significance of the presence of a few things and the absence of many. The sokition seems to be relatively simple and to involve nothing more subtle than the composition of the fossil remains. Virtually the only shells and tests that are preserved intact are those that are composed of calcite; that is, brachi- opods, echinoids, oysters and Pectens among the lamelli- branchs. and Epitonids among the gastropods. One of the Epitonids (locality 445) is badly leached, but the Opalias are perfectly preserved. The host of mollusks with less durable aragonite shells are not represented at all or are sparsely represented at a few places by impressions and molds, to which some of the shell may still be attached, with the exception of the Forrcria, which consists of a shell fragment, and the Monia. which is perfectly preserved aside from the loss of the inner nacreous layer. The collections consist principally of a monotonous repetition of oysters, which are the most abun- dant fossils, and Pectens, of which there is a surprising num- ber of species, with an addition of brachiopods and echinoids here and there. In Temescal Canyon brachiopods are extra- ordinarily abundant and present an amazing range of vari- ation, but at this locality echinoids are represented by only a few small spines. The fossil-bearing bed in Temescal Canyon consists of coarse sandstone and north of Simi Valley the beds are coarse sandstones and conglomerates. The water that readily percolated through these porous beds quickly dissolved the aragonite shells. Furthermore, the absence of even molds of aragonite-shelled mollusks at most localities indicates that the shells generally were dissolved before the sediments were cemented. Unless some fine-grained sediments are found, there seems to be little hope of obtaining a representative col- lection from these deposits. PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES Fourth Series Vol. XIX, No. 7, pp. 65-83, 3 text figs. July 15, 1930 VII GEOLOGY OF SHARKTOOTH HILL, KERN COUNTY, CALIFORNIA BY G. DALLAS HANNA Curator, Department of Paleontology Introduction In order to explain the geology of Sharktooth Hill and the strata from which were obtained the fossils which are to be described in the Academy's Proceedings, it has been necessary to give consideration to some of the surrounding area. The information has been accumulating through a period of years but even yet, it is believed, insufficient work has been done to warrant more than a general statement regarding some of the points discussed. Undoubtedly this will be looked upon as a deficiency by those who have pursued much more detailed studies in certain cases, but it is felt that the course followed has obviated any very serious errors. So many people have contributed to make this report pos- sible that it is impracticable to mention all. However the friendly spirit of cooperation which has been invariably shown is most deeply appreciated. July IS, 1930 56 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Location Sharktooth Hill is located on the north side of Kern River in Sec. 25, T. 28 S., R. 28 E., M. D. M., Kern County, Cali- fornia. This is about seven miles northeast of Bakersfield. The hill is a somewhat isolated prominence set back from the river about one-fourth mile. The elevation is given as 643 feet on the Caliente sheet of the U. S. Geological Survey's topographic map, but the hill is not named thereon. The road to the Round Mountain oil field passes to the south. The section on which Sharktooth Hill is located belongs to the Southern Pacific Land Company. History The locality has long been known for the great numbers of teeth of sharks which might be picked up from the surface of the slopes of the hill. Large collections of these are in numer- ous museums. Several species of sharks are represented and the size of the teeth varies from a length of 10 millimeters in Gyrace to over 100 millimeters in the giant Carcharodon. Much study has been devoted to these teeth in the past by Louis Agassiz, David Starr Jordan and his associates; a list of important publications is given below/ ' Agassiz, L. Notice of fossil fishes found in California by W. P. Blake. Amer. Jour. ScL & Arts, ser. 2, vol. 21, 1856, pp. 272-275. Notice of the fossil fishes. Explorations and surveys for a railroad from the Mississippi River to the Pacific Ocean, vol. 5, 1857; Geological Report by William P. Blake, Appen- dix, Article 1, pp. 313-316, pi. 1. Jordan, D. S. The fossil fishes of California with supplementary notes on other species of extinct fishes. Univ. Calif. Publ. Bull. Dept. Geol. vol. 5, no. 7, 1907, pp. 95-144, pis. 11, 12, 33 text figs. Leriche, Maurice. Observations sur les Squales Neogenes de la Californie. Annal. Soc. Geol. du Nord, vol. 36, 1908, pp. 302-306. Jordan, D. S. & C. H. Beal. Supplementary notes on fossil sharks. Univ. Calif. Publ. Bull. Dept. Geol. vol. 7, no. 11, 1913, pp. 243-256, 8 te.xt figs. Jordan, D. S. & J. Z. Gilbert. Fossil fishes of the (Miocene) Monterey formations of Southern California. Leland Stanford, Jr. Univ. Publ. Univ. Ser., in 'Fossil fishes of southern California," art. 2, 1919, pp. 13-60, pis. 1-31. Jordan, D. S. Some sharks' teeth from the California Pliocene. Amer. Jour. Sci. ser. 5, vol. 3, 1922, pp. 338-342, 9 text figs. Jordan, D. S. & H. Hannibal. Fossil sharks and rays of the Pacific Slope of North America. Bull. Southern Calif. Acad. Sci. vol. 22, pt. 2, 1923, pp. 27-63, pis. 1-14. Leriche, M. Les Poissons Neogenes de la Belgique. Mem. Mus. Roy. d'Hist. Nat. Belgique, no. 32, 1926, pp. 365-472, pi. 28-41. Vol. XIX] HANN A— GEOLOGY OF SHARKTOOTH HILL 67 Fig. 1. Part of U. S. Geological Survey, Topographic Map, Caliente Sheet, Kern County, California, showing Sharktooth Hill and other prominent points. 68 CALIFORNIA ACADEMY OF SCIENCES [ Proc. 4th Se«. No record has been kept of the many visitors who have gone to the hill for the purpose of collecting teeth, but the number is very large. One of the first to make a fairly repre- sentative scientific collection, however, was Mr. Frank M. Anderson, long associated with the Department of Paleon- tology of the California Academy of Sciences. His material was studied by Jordan & Beal in their report on fossil fishes of California. Before that, that is in November 1909, Mr. Charles Morrice was attracted to the locality because of its fossils. He was employed by the Pacific Oil Company and stationed at Oil Center near the eastern margin of the Kern River Oil Field. This was sufficiently near to Sharktooth Hill so that he could spend his leisure hours there collecting. He soon located the stratum which had produced the teeth found weathered out on the surface and a vast number, beautifully preserved, came into his collection. Always generous and considerate of others' wishes, Mr. Morrice distributed his finds widely and they formed the very foundation of some studies of fossil sharks subsequently undertaken. Fortunately, through the kindness of Mr. Morrice, I am able to give his own account of his many years as a collector of marine vertebrates at this locality. Under date of December 10, 1929, he wrote as follows: "I first became interested in collecting fossils about November, 1909. Some of my acquaintances, observing that I took long excursions on Sun- days asked me if I had ever visited Sharktooth Hill. I had not and it took me several weeks to locate it. Once found, my hobby became col- lecting sharks' teeth. "All of the teeth which had been gathered at the place up to this time, as well as those in the collection which had been made by Mr. Barker on his ranch on the south side of the river had been more or less leached by exposure to the weather. This is evident from the illustrations in the paper on fossil fishes of California by Dr. David Starr Jordan, pub- lished in 1907.2 "I carried, first a pick and then a shovel to the hill, which was about five miles east of my residence, and made an excavation about four or five feet deep. This resulted in securing many beautifully preserved = Jordan, D. S. Univ. Calif. Publ. Bull. Dept. Ckol. vol. S, no. 7, 1907, pp. 95-144, pU. 11, 12. Vol. XIX] HASfNA— GEOLOGY OF SHARKTOOTH HILL 59 Specimens in a fine, hard silt or mud which eflfectively protected the enamel of the teeth. "In about six months I had gathered several hundred specimens and! having become acquainted with Mr. F. M. Anderson I showed them to him. He suggested that I write to Dr. Jordan for a copy of his paper referred to above, in order that I might be able to classify the collec- tion. This I did but my letter was lost, much to my chagrin. Some months later I told Mr. Anderson of my failure to receive the copy of the paper and he promised to send me his own, which he did. When Dr. Jordan finally learned of my eflforts and desire for literature on the subject he very courteously sent me an autographed copy. "By early 1912 my collection amounted to about 2,000 specimens, in- cluding bones and teeth of the sea lion, later named Allodesmis kemensis by Dr. Kellogg. Upon consulting Mr. Anderson as to the disposition of the material, he suggested three institutions worthy of receiving it, namely: Stanford University, University of California and California Academy of Sciences. "After due consideration I sent the entire collection to Mr. Anderson for the California Academy of Sciences for such disposition as might seem best. It was suggested that only duplicates be given to other institutions. "In about six months more I had g^athered together about 1,500 addi- tional specimens. These I sent to Dr. Jordan for Stanford University and they, with the collection already presented to the Academy, formed the basis of the good Doctors' 'Supplementary notes on fossil sharks' published in 1913.8 "My next collection of over 1,000 specimens was sent to Dr. J. C Merriam for the University of California. Other collections made later were sent to: University of Neveda; University of Wisconsin; Southern California Academy of Sciences ; Universities of Lille, France ; Brussels, Belgium; Aberdeen, Scotland; and to the High School and Chamber of Commerce of Bakersfield, California. "During the summer of 1922 Dr. Remington Kellogg and Dr. Bruce L. Qark of the University of California, accompanied by several other gen- tlemen, visited me and we made an excursion to the Sharktooth Hill deposit. In a short time we uncovered enough bones to arouse their interest. At Dr. Kelloggfs request I began sending fossil bones to him at the U. S. National Museudi and this continued imtil 1924 when the skull of Aulophyseter morricei was shipped. "In the fall of 1924 through the interest of the California Academy of Sciences, Mr. Tom Harbert was employed during October, November and December and the large collection being described by Dr. Kellogg was then obtained. "Dr. Jordan visited me in 1923 and again in 1924; large collections were given him on each occasion. Some of these specimens were used •Jordan, D. S. 4 C. H. Bcal. Univ. Calif. Publ. Dept. G«ol. voL 7, n©. 11, 1913, pp. 243-256, 8 text figs. 70 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Sf.r. in the paper published by the Southern California Academy of Sciences in 1923 by him and Harold Hannibal.* "Along with the teeth of sharks there were many ear bones of dolphins and bones of seals and sea lions which Dr. Jordan transmitted to Dr. Kellogg. "After every shipment of bones to Dr. Kellogg he wrote very interest- ing accounts of the 'finds'. These consisted of bones of dophins, por- poises, seals, sea lions, whales and sea cows. His letters were so inspiring that it was indeed a pleasure to have worked with him. My greatest regret is that I did not make his acquaintance at an earlier date so that many specimens of bones, cast aside in the search for sharks' teeth, might have been preserved." Previous to Dr. Kellogg's visit in 1922, Mr. Morrice had already saved a considerable number of bones and teeth of what appeared to him to have belonged to one species of animal. These, together with material obtained by the two collectors together formed the basis for Kellogg's description of the sea lion, Allodesmis kernensis.^ 3t became evident from the work done up to 1924 that the stratum exposed on Sharktooth Hill contained an enormous number of bones and teeth of marine vertebrate animals. Remains of whales and sharks were particularly abundant and the sperm whale Aiilophyscter morricei was described from the collection sent to the National Museum.^' Up to that time no reasonable hypothesis had been evolved to account for the anomalous disassociation of all skeletal ele- ments of the animals and the fragmentary nature of many of the bones. The California Academy of Sciences entered into correspondence with Dr. Kellogg and Dr. John C. Merriam of the Carnegie Institution of Washington on the subject and conferences were had with Mr. Morrice, Mr. M. E. Lombardi, then Vice President of the Pacific Oil Company and with Messrs. J. E. Taff and E. G. Gaylord, Geologists for the com- pany. After due consideration of all interests and factors it ♦Jordan. D. S. & H. Hannibal. Bull. Southern Calif. Acad. Sci. vol. 22, pt. 2, 1923, pp. 27-63, pis. 1-14. •Kellogg, R. Univ. Calif. Publ. Geol. Sci. vol. 13, no. 4, 1922, pp. 26-114, 19 text figs. ^ Kellogg, R. Study of the skull of a fossil spverm-whale from the Temblor Miocene of southern California. Carnegie Inst. Washington, Publ. no. 346, 1927, pp. 1-24, pis. 1-9. Vol. XIX] HANt/A— GEOLOGY OF SHARKTOOTH HILL /J was decided early in 1924 that the Academy should undertake some more extensive excavations than had theretofore i)een attempted. The field work was under the immediate supervision of Mr. Morrice whose services were gratituous. Mr. Tom Harbert was employed as assistant continuously for the last three months of 1924, and it was during- this period that the greater part of the collection to be reported upon by Dr. Kellogg was obtained. This report amply illustrates the wealth of material in the Sharktooth Hill deposit. The author has commented at times on the unfortunxite disassociation of the skeletons and the fragmental nature of many of the bones. The preserva- tion is normally very good, but how to account for broken pieces of limb bones and ribs in close proximity to vertebra and other delicate bones is a problem for which no satisfactory solution has yet been suggested. Geologic Section The total thickness of sediment exposed on Sharktooth Hill is about 200 feet. The strata dip to the southwest at low angles, the maximum being about 6°. The top of the hill is composed of unconsolidated sands and gravels belonging to the Kern River Series with an important unconformity at the base. This unconformity is not characterized by any very noticeable discordance in dip or strike of the strata, but it is known that it marks the absence of several thousand feet of sediment. On Sharktooth Hill the contact is not well exposed but the upper layer of the Temblor outcrops as a consolidated sandstone containing many fossil mollusca. This outcrop is within 50 feet of the top of the hill on the southeast side. Between the shell layer and the bone bed there is a zone of 30 feet of loosely consolidated sands and sandy shales not well exposed. The bone bearing layer itself is about four feet thick with the bones and teeth most abundant near the bottom. The matrix is loosely consolidated and poorly sorted sand with occasional small pebbles. The bone and shell beds 72 CALIFORNIA ACADEMY OF SCIENCES [Pnoc. 4th Ser. together constitute the type locality of zone "C" of F. M. Anderson.* Below the bone bearing stratum there is a zone of brown sandy shales about 30 feet thick which have contained abun- dant foraminifera, but on this outcrop the tests have been dis- solved away leaving poor impressions. The presence of the large, characteristic Valvidineria of this part of the Miocene is easily determined, however, with a hand lens. The diatomite from which the flora to be described in a suc- ceeding paper was obtained, outcrops immediately below these sandy shales and extends downward to the base of the hill. All of the diatom bearing material is somewhat impure, acidic ash being the chief mineral constituent. Some of the layers are light and "punky" and all of them weather to a pxale brown color. The total thickness exposed is 75 to 100 feet. The identification of this horizon over wide areas has been dealt with in the paper describing the flora. The total exposure of strata on Sharktooth Hill is not suf- ficient to permit a general statement pertaining to the entire Miocene section of this area, but it so happens that several wells have been drilled nearby. These have been cored almost continuously and furnish extremely reliable sectional data. This will be presented in some detail, but before doing so it will be desirable to comment on the geographic extent of the outcropping and related beds. The shell layer mentioned as occurring at the top of the section is of exceedingly limited distribution. It has not cer- tainly been identified elsewhere by me except on a hill south of Kern River and just west of the lower portion of Cotton- wood Creek. The presence of Turritella ocoyana Conrad is sufficient evidence to indicate the Temblor age of the material. In contrast to this the bone bearing stratum is of very wide distribution on the east side of the valley and has been identi- fied in many outcrops. The southernmost exposure lies far to the south of Sharktooth Hill on the divide between the Caliente Creek and Kern River drainage. Sharks' teeth col- lected there by F. M. Anderson and Harold Hannibal were • Anderson, F. M. The Neocene deposits of Kern River, California, and the TemWor Basin. Proc. Calif. Acad. Sci. ser. 4, vol. 3, 1911, p. 85. Vol. XIX] HANNA— GEOLOGY OF SHARKTOOTH HILL 73 described by Jordan & Hannibal, the locality being usually indicated as "Bena," a station on the Southern Pacific Rail- road nearby." Traces of bones and teeth may also be found on the old Barker Ranch on the south side of Kern River in Sees. 5, 6, T. 29 S,, R. 28 E. The diatom horizon outcrops at the river and the structure is so complicated by faulting that the thick- ness between it and the bone layer could not be determined although it seemed to be greater than on Sharktooth Hill. In a northwesterly direction from the hill the bone layer can be traced by outcrops far to the north, to the old "Fullers Earth Mine" on Granite Creek three miles north of Poso Creek. The matrix at this point is more ashy and less sandy than at Sharktooth Hill and the bones and teeth are found through a vertical thickness of at least 30 feet. However, they are much more abundant in the lower portion of the exposure. Another outcrop has been brought to the surface by faulting in a branch of Granite Creek coming from the northwest. This is in the northeast corner of Sec. 28, T. 27 S., R. 28 E., M. D. M., and probably is the locality from which Blake made a collection of sharks' teeth during the progress of the Pacific Railroad Survey.^ The sandy shales mentioned as lying between the bones and diatomite in the Sharktooth Hill exposure form a part of what has come to be recognized by all working geologists of the region as the " V alvulineria zone." Outcrops are numerous and usually unmistakable although the fossil from which the zone takes its name has a vertical range of probably 500 feet. In fact it extends upward into the base of the Montery at the type locality near the town of that name. The association of foraminifera found at the two localities has been the means of determining that the top of the Temblor in this Kern River section is very nearly the stratigraphic equivalent of the base of the type Monterey. The difference, if any, cannot amount to more than a few hundred feet of strata. It is extremely probable that the diastrophism which caused the termination 'Jordan, D. S. & H. Hannibal. Bull. So. Calif. Acad. Sci. vol. 22, pt. 2, 1923, pp. 27-63. •This collection was described by Louis Agassiz in 1856 and 1857; see footnote BO. 1. 74 CALIFORNIA ACADEMY OF SCIESfCES [Proc. 4th Se«. of marine sediineiitation on the east side of the San Joaquin Valley initiated the same in the Monterey area. In many localities where sedimentation was continuous throug-h the period it becomes impossible to draw a sharp line of contact between the Temblor and Monterey. This unfortunate cir- cumstance has resulted in the identification of a group of strata as the older formation by some paleontologists while others have referred the same beds to the younger. The situ- ation is complicated in other ways and requires very careful analysis. In the immediate vicinity of Sharktooth Hill, exix)sures are lacking which furnish information on the strata directly below the zone of diatomite at the base of the hill. East of the hill, which normally would be down deeper in the section there is a major fault, striking in a general north-south direc- tion. The west side of this fault is upthrown several hundred feet ; to the east, therefore, for a considerable distance, the formations are marked by Kern River Series and terrace deposits. At the point shown on the map near the letter "K" of "Kern" in the northeast corner of Sec. 5. T. 29 S., R. 28 E.. there is a prominent exposure of gray, loosely consolidated sandstone charged with beautifully preserved molluscan fossils. The locality has furnished many striking new species, described chiefly by Anderson & Martin." The bed became "zone B" of the first author.'" The fauna of this zone has become very well known because of the excellent preservation of the fossils and it is often referred to as the Agasonm barkcrianum zone of the Temblor. Conrad'* described the first fossils from it in 1855 chiefly from sketches of casts and molds made by W. P. Blake at an unknown locality probably on Poso Creek a few miles to the north. Cooper'- in 1894 added to the list of species, from • Andei-son, F. M. & B. Martin. Proc. Calif. Acad. Sci. ser. 4. vol. 4, 1914, pp. 15-112. pis. 1-10. "Anderson. F. M. Proc. Calif. Acad. Sci. s«r. 4. vol. 3, 1911, p. 85. " Conrad, T. A. Pacific U. R. Repts. House Doc. 129, 33rd Cong. 1855, pp. 18-20; Quarto Rept. vol. S, 1857, pp. 328-329, pis. 7-9. " Cooper, J. G. Catalogue of California Fossilii. Calif. State Mining Bureau, Bull. 4, 1894, pp. 53-54. Vol. XIX] HANNA— GEOLOGY OF SHARKTOOTH HILL 75 material collected across the river to the south of the zone B locality, on the old Barker Ranch. The zone B locality is far enough to the east of Sharktooth Hill so that if the horizontal distance be projected with the dip of the beds there is an apparent vertical distance of approximately 500 feet between it and zone C ; this figure was computed by F. M. Anderson in defining the zones, but the intervening faulting was not noted. Actually the two zones are not widely separated vertically. They are really sandy phases of the upper part of the Temblor of this area, and in no cases are they of wide areal extent in the region. (Refer- ence is made only to that part of "zone C" at the top which contains the fossil mollusca.) The zones are too indefinite and inconstant in lateral distribution to answer the needs of present day stratigraphy and have been practically replaced for map making purposes by the much more persistent zones of micro-fossils. Identifiable molluscan fossils are rarely found in the collections made in drilling wells and it is these which have furnished the most complete and reliable information on the geology of region. Below these molluscan bearing sands of the upper Temblor there is a succession of sandy shales carrying an abundance of foraminifera. They might all be classed in the general term "Valvulineria zone" but differences in the succession of strata show changes in the assemblage of species and the abundance or rarity of particular species ; for this reason more or less subdivision is practicable but the details vary among the dif- ferent workers. This subdivision will not here be discussed because it should accompany a detailed discussion of the foraminifera which is yet to be made. This zone of foraminif era-bearing shales is followed by several hundred feet of light gray ashy shales, practically barren of fossils except fish scales and bones. The thickness probably varies between 1000 and 1500 feet in most cases. Occasional shells are scattered through and foraminifera are found sparingly at several places, thus affording a means for zonal subdivision in some of the most detailed work which has been undertaken. Lithologically there are changes embodying clay, silt, fine sandy shale, fine sand, ashy shale and July IS, 1939 75 CALIFORNIA ACADEMY OF SCIENCES [Puoc. 4th Skr. occasionally hard calcareous lenses. These variations are inconstant in distribution, and it is not believed that any of them, taken alone are now used for correlation purposes. Toward the base of the ashy shale series, however, this material takes on a peculiar form which can often be recoj^- nized. The background is pale pearl-gray ashy shale and dis- seminated throughout there are irregular thin black or dark gray lines, extending in every direction, abundantly but not crowded. The appearance has suggested the name "hair shale zone." The layers of material having this character are limited in thickness and seem to be absent in some cases. How- ever, the zone is accompanied by a very striking assemblage of foraminifera found widely distributed in this region and in many other places in California, Oregon and Washington. The zone is approximately 250 to 275 feet thick. It outcrops on Adobe Creek (a north branch of Poso Creek) where a major fault has lifted the strata on the east several hundred feet. Immediately below this hair shale zone about 250 to 300 feet of ashy and sandy shales carry a fauna of foraminfera in which Siphogenerma is dominant. This, likewise, is widely distributed in the west although I do not know that it outcrops in the Kern River Region. From this point on down to the base of the Temblor the sediments are predominantly sandy with some strata of gravel and conglomerate. The thickness is extremely variable, as might be expected, but an average of 600 feet suggested for the area may not be far wrong. Fossils are notably scarce in the cores taken from wells; enough moUusca have been found, however, to identify the zone definitely with the sandstone strata which outcrop on Pyramid Hill along the granite contact at the east side of the valley. The hill is in Sec. 14, T. 28 S., R. 29 E. and about five miles east northeast of Sharktooth Hill. A large and striking assemblage of fossil mollusca has been obtained on Pyramid Hill and, being near the base of the Temblor section, the locality was designated "zone A" by F. M. Anderson. ^^ Anderson, F. M. Proc. Calif. Acad. Sci. »er. 4, vol. 3, 1911, p. 85. Voi_ XIX] HANNA— GEOLOGY OF SHARKTOOTH HILL jy The same zone is found at Comanche Point at the south end of the valley and has been tentatively identified at some places on the west side. The Temblor rests on an uneven surface of a series of green, red and blue, often mottled, clays, sandy shales, sands and gravels. These have much the appearance of being of continental origin. They are pratically non-fossil bearing and have come to bear the name "Walker formation" because there is a limited exposure in Walker Basin Creek in the southeast corner of the valley. At that point the shales contain sparingly, fossil land shells but these have not yet helped in determining the age of the formation. Some have thought them to be the equivalent of the Sespe formation, but they may be a phase of the Vaqueros Miocene. There are limited outcrops of the material on Pyramid Hill and to the north as far as the point where Granite Creek issues upon the valley plain. Excellent exposures are found at Comanche Point beneath the Temblor. At none of these places can an adequate conception of thickness be obtained and data derived from the few wells which have penetrated the formation are equally misleading. For the sake of record, however, it should be stated that in Sec. 4, T. 26 S., R. 27 E., M. D. M., the thickness of the Walker was 172 feet. In most of the wells which have gone through the Walker clays and sands, granite has been encountered. But in one limited area which includes Sees. 16 and 22, T. 26 S., R. 28 E., M. D. M., the basement rock was slate or shistose rock which possessed all the physical characters of the Mariposa, found outcropping far to the north. The areal geology of the Kern River Region is now known to be characterized by an extremely complicated system of faults. These have probably resulted from major and minor fractures in the underlying granite. An idea of their extent and general character can probably best be obtained from a study of the granite itself as exposed a few miles to the east- ward where joint planes and faults of some significance are extremely numerous and highly irregular in trend. And the locations where some of the more obvious breaks occur in the 78 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Sek. valley sediments are very well described and shown on a map in a late report by Mr. Leo S. Fox." The following sections of two representative and thoroughly sampled wells drilled in the vicinity of Sharktooth Hill are offered to support the statements already made. I am deeply indebted to my associate, Mr. C. C. Church, for the prepara- tion of these sections and much other assistance through a period of years. Two formation names have been omitted from these sec- tions which some geologists would indicate. These are Chanac and Santa Margarita. The first has been applied to a certain zone of material which is lithologically very much like parts of the Kern River series but it lies below some marine shales and sands which appear to be Etchegoin Pliocene. The name was originally given to a certain landlaid deposit at the south end of the valley from which imperfectly preser\^ed vertebrate fossils have been collected. The evidence to support the theory that the sediments found in the wells about Bakersfield are equivalent in age to the type locality is very meager and is too insecure at this time, it seems to me, to justify the trans- plantation of the name so far. The basis for recognizing Santa Margarita (upper Mio- cene) in the wells of the Kern River District is likewise extremely unsafe. Below the clays and sands called Chanac there is found a marine zone of sediments containing some f Oram inif era which are different from typical upper Temblor and upper Etchegoin and it is to this zone that the name has been applied. Some competent geologists believe that the evidence indicates an interfingering or overlapping of marine and landlaid material early in the Pliocene because the dis- tinctions have been proved to disappear farther out in the valley from the eastern shore line. The fossils found in the so-called Santa Margarita of the wells are not sufficient for this determination because no foraminifera have been found at the type locality of that formation ; at least none have been reported. " Fox, Leo S. Structural features of the east side of the San Joaquin Valley, Cali- fornia. Bull. Araer. Assoc. Petrol. Geo!, vol. 13, no. 2, 1939, pp. 101-108. map fig. 1. Vol. XIX] HANNA— GEOLOGY OF SHARKTOOTH HILL 79 "^cnes/n Mef /ooo Zones J.Sff*. IC£ c; /eso /osa , sooo so C 2oao. es 16? * ^CS3 J .■^£<)S A(?r/7 /v'/t^e'r4r ^one *Stf>^o^f7er/f^ J^Cne ^ec^i^r Scftt/ /r/c/7/7e/d'0//Co. j^osronA/o./ j^em Co.. Cc?///b/7r7/a. ■-< Ms/Zrer ' rejon r^j Fig, 2. Section shown in drilling Richfield Oil Company Well, Boston No. 1, near Sharktooth Hill. gQ CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Se«. Part of the difficulty has arisen from the supposed existence of Santa Margarita at Comanche Point at the south end of the valley. A very considerable collection of moUusca has been made there for the Academy and this has been critically exam- ined by Messrs. F. M. Anderson and L. G. Hertlein. They advise that the large oyster found in the collection is not Ostrea titan and the pecten is not Pecten crassicardo. The original determination was based on the supposed presence of these two species. The collection contains several species not yet known from upper Miocene or later deposits any place in California. General Correlations An attempt will not be made here to give a chronological account of the various efforts which have been made to cor- relate this part of the Temblor with sediments widely distrib- uted elsewhere. It is believed the needs of the present study will be fulfilled by presenting the conclusions reached by those who have most recently taken up the subject. Dr. W. P. Woodring^® in 1928 in a comprehensive study of the Mollusca of Bowden, Jamaica gave a large number of Miocene correlations and these have much wider application than can be inferred from the title of the paper. Regarding the Temblor he stated (p. 98) : "By means of this indirect comparison and relying for the most part on the admittedly slender evidence of one phylum of Turritellas it is con- cluded that the Bowden formation is about the same age as the Temblor formation, or as the upper part of the Temblor formation." He placed the Bowden in the upper Middle Miocene, the equivalent of the Tortonian of the European standard time scale (p. 39). On another page (p. 94) the Calvert formation of the Chespeake Bay area is likewise correlated with the Tor- tonian, chiefly on the basis of studies of the plants and marine mammals by Berry^* and Kellogg^'' respectively. " Woodring, W. P. Miocene mollusks from Bowden, Jamaica. Pt. 2. Gastropoda and discussion of results. Carnegie Inst. Washington, Publ. 385, 1928, pp. 1-S64, pis. 1-40, 2 text figs. "Berry, E. W. U. S. Geol. Surv. Prof. Ppr. 98-F. 1916, pp. 61-70. "Kellogg, R. Bull. Geol. S«c. America, vol. 35. 1924, pp. 763-764. Vol. XIX] HANNA— GEOLOGY OF SHARKTOOTH HILL 81 ^o^Sis /h Zee/- -£fe«i^ JS^a"^ ^^fyoyerrery'frir ^of^ l^eZ 10.5 .31 II I 12 I 9 30 VI. 27 8 .30 II I 12 I 8 * VII. 27 8.5 .31 II I 11 I 9 — VIII. 29 10 .34 II I 12 I 9 — IX. 37.5 12 .32 II I 12 I 8 — ♦Not examined in last four specimens. Vol. XIX] MYERS— THE KILLIFISH OF SAN IGNACIO IQ3 LITERATURE CITED* ElGENMANN, C. H. 1892. The fishes of San Diego, California. p- high, and a gradually attenuated tip which is both capitate and calyptrate. They seem clearly to belong to this widespread species. Family Nostochace.e HORMOTHAMNION Grunow, Reise der Novara, Algen, 1867, p. 31, pi. 1, fig. 2 16. Hormothamnion enteromorphoides f. gracilis, f. nov. Filaments parallel, agglutinated into strands; sheaths thin, hyaline, often confluent; trichomes 4.5-5.5 /u. diam., apex slightly attenuated; cells broadly dolioform to compressed- spherical, apical cell blunt-conical ; heterocysts the same shape as the cells, slightly larger. In strand-like, gelatinous masses intermingled with other algse. Mason, Nos. 61a, 62, 105, 113a, 117, and 138. Guada- lupe Island. 124 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Type: No. 173643, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 117), in April, at Guadalupe Island. A species seeming to belong to this genus occurred in fre- quent admixture in the Guadalupe collections. It was per- sistently sterile, but its short, compressed cells, its more or less compressed heterocysts, its distinct gelatinous sheath, seemed to separate it from Anabcuna, and the strikingly paral- lel arrangement of the trichomes seems to point towards Hovmothamnion. Its trichomes 4.5-5.5 /* in diameter and attenuate at both ends seem to indicate possible closeness to H. enteromorphoides Grunow, but it is somewhat more slender than the plant described by Grunow (Alg. Novara) from Ton- gatabu. The parallel arrangement of the trichomes much like those of a Phormidium is definite, but the gross habit and original color could not clearly be determined from the admix- tures of algae preserved in alcohol. It has shorter cells than those described for H. convolutiim Collins and Hervey (1917, p. 24), and while we refer it provisionally as a slender form to H. enteromorphoides we also feel that it may prove to be a distinct species. Family Rivulariace^ CALOTHRIX AG.\RDn, Syst. Alg., 1824, p. XXIV 17. Calothrix codicola sp. nov. Plate 4, fig. 4 Filaments 14-16 /* diam. at the slightly enlarged base, almost cylindrical to the short-tapering apex, 400-600 n. long; trichomes 10-12 /* diam. at the base, tapering very gradually toward apices terminating in a short hair when young, in the lower parts slightly constricted at the cross walls ; cells bright blue-green, quadrate to slightly longer or shorter, contents homogeneous; heterocysts basal and intercalary, 1-3 at the base, when single slightly narrower than the trichome and subspherical, when more than one, the others in the series 1.5-3 times as long as the diameter ; sheath close fitting throughout, thin, smooth, homogeneous, hyaline. Growing among the utricles of C odium fragile (Suringar) Hariot, in company with Brachytrichia codii Setchell. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALG£ 125' Type: No. 173636, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 39), in April, at Guadalupe Island. Codiuni species seem to be favorable hosts for various minute members of Myxophycese, as well as of other groups of marine algae. It is to be questioned as to whether the peculiarities of the Codium exercise such an influence on these various epiphytes (or endophytes) as to modify their struc- ture and particularly their habit, from what they might assume upon hosts of other consistencies, owing to possibly peculiar ease of penetration. The Calothrix described above seems to' differ so much from any of the epiphytic species described and to come so much closer, perhaps, to some of the rupicolous species, that we hesitate to assign it definitely. It differs from both C. coruginea Thuret and C. parasitica Thuret, in diameter of filament and trichome sufficiently to be regarded as distinct, and it differs also in cell proportions from both of the cited species. It is not bulbous at the base as is C. parasitica. Our plants seem to branch, but possibly the branches may represent epiphytic plants of hormogonial origin, at least the branches resemble the similar structures of C. Crustacea Thuret (cf. Notes Algol., Fasc. 1, pi. IV). The cell proportions in our specimens differ from those of C. Crustacea. 18. Calothrix Crustacea Thur. Growing on rocks in company with other Myxophyceae. Mason, Nos. 42, 107, 115. Guadalupe Island. Thuret, in Bornet and Thuret, Notes Algol, fascicle 1, 1876, pp. 13-16, pi. 4. Calothrix Crustacea Thuret is a variable species, usually characterized by its size, intercalary as well as basal hetero- cysts, and its distinct hyaline sheath, occasionally yellow below. Typically it forms an seruginous layer on rocks, but often occurs also epiphytic on broader or more slender algse. It is unbranched, but very commonly is infested more or less with epiphytic filaments of the same species which have arisen from the usually abundant hormogonia (cf. Bornet et Thuret, Notes Algologiques, pi. 4). This gives such plants the superficial appearance of being branched. Our specimens seem to agree December 30, 1930 125 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Skr. in all details with typical C. cntstacea Thuret. but exceed the published measurements as to diameter of trichome (10-20 /*). 19. Calothrix confervicola (Roth.) Ag-. Growing on Laurencia. Mason. No. 46. Guadalupe Island. Agardh, Syst., Alg., 1824, p. 70. Conferva confervicola Roth, Cat. Bot, fascicle 3. 1806, p. 193. This occurs in stellate clusters on the host and seems typical, although the natural color has been changed by being pre- served in alcohol. The sheaths are homogeneous and hyaline, thus distinguishing it from C. consociafa Born, and Thur. 20. Calothrix clausa sp. nov. Plate 4, fig. 5 iMlaments 30-34 /x diam., 500-600 /i up to 1 mm. long, tor- tuous ; trichomes 24-28 /i diam., cylindrical except at the short, tapering apices, ending in a short, narrow hair, constricted prominently at the cross walls, bright blue-green; cells 3-4 /* long, with homogeneous contents uniform throughout the filament; heterocysts basal and intercalary, solitary, same diameter as the trichome, hemispherical to elongated-cylindri- cal ; sheath hyaline, homogeneous, smooth, close fitting, for the most part closed at the apices. Growing in association with other Myxophyce^e on rock. Type: No. 173629, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 59), in April, at Guadalupe Island. The species, proposed as new, is a member of the Calothrix confervicola group, with trichomes thicker than any of its other members, and showing, at least so far as the type speci- men is concerned, a sheath normally contracted even to cloture at the apex. It seems desirable to describe it as new. 21. Calothrix aeruginea var. abbreviata var. nov. Filaments 9-11 ^ diam. at the base, 130-150 /i long, decum- bent for considerable distance at the base or in the middle and turning upward at both ends; trichomes 7-8 m diameter at the Vol. XIX] SETCHELL AMD GARDNER— THE MARINE ALGAI 127 base, not bulbose, tapering gradually from the base to the apex, ending in a short, slender hair ; cells quadrate or shorter, very slightly constricted at the cross walls; heterocysts basal, hemispherical, of the same diameter as the trichomes, single, or rarely two, at the base ; sheath very thin, smooth, homogene- ous, hyaline, not ocreate. Growing on Ectocarpus Duchassaingianus. Type: No. 173617, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 113), in April, at Guadalupe Island. u-i i L I B f< A R Y I 22. Calothrix sp. A single tuft of a very slender Calothrix seems nearest to the plant described under C. epiphytica W. and G. S. West (in S. and G., Mar. Alg. Pacific Coast N. A.) or Gardner's C. linearis from Porto Rico. The trichomes show bulbous en- largements at the base and are very slender. They measure 4-5 /t diam. at the base, 2.5-3 /* above, and 175-225 /x. long. Mason, No. 33a. Clarion Island. DICHOTHRIX Zanardini, Plant Mar. Rubri Enumer., 1858. p. 89 23. Dichothrix sp. (Growing among other minute algae on rocks. Mason, No. 149. Guadalupe Island. A few fragments of a very slender species, seemingly of Dichothrix have been noted in one of our preparations. The trichomes are slender (6-8 fx. diam), somewhat swollen at the base, with heterocysts exceeding the diameter of the trichomes and with hyaline, gelatinous sheaths. The material is insuf- ficient for description of a new species and it does not seem to agree with any that are described. It is noted for the informa- tion of future explorers. SCYTONEMATACE.^ MICROCHJETE Thuket, Essai, 1875, p. 7 24. Microchaete vitiensis Askenasy Associated with other species of Myxophyceae. sparse. Mason, No. 137. Guadalupe Island. Very 128 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Seb. Askenasy, in Bornet and Flahault, Tab. Syn. Nostochacees, 1885, p. 22. A minute alga, clothing other slender, filamentous algae, looking like a small Calothrix, with curved base, but the apex of trichome blunt and not at all attenuate. It has been detected on the coasts of Fiji (type), Samoa, and Tahiti. In the Guadalupe specimens, the cells are shorter than in the type. STIGONEMATACEA^: BRACHYTRICHIA Zanardini, Phyc. Ind. Pug., 1872, p. 24 25. Brachytrichia Codii Setchell Among the utricles of C odium fragile. Mason, No. 143, Guadalupe Island. Setchell, Tahitian Alg., 1926, p. 66. This pholadophyte (or snuggling) species of Brachytrichia, described from Tahiti, but also noted from Hawaii, may now be reported from Guadalupe Island. CHLOROPHYCE,^ Family Caulerpace^ CAULERPA Lamouroux, Mem. sur la Caulerpes, 1809, p. 141 26. Caulerpa racemosa var. clavifera f. macrophysa (Kuetz.) Weber-van Bosse Mason, No. 58. Guadalupe Island. Weber-van Bosse, Monogr. des Caulerpes, 1898, p. 361, pi. 33, fig. 4. Chauvinia macrophysa Kuetzing, Tab. Phyc, vol. 7, 1857, p. 6, pi. 15, fig. 2. The plants collected were close to this form except that the swollen ramuli were only slightly over 2 mm. in diameter. Our plants therefore incline towards f. microphysa W.-v. B. The type is from Central America. 27. Caulerpa racemosa laetevirens f. cylindracea (Send.) Weber-van Bosse Mason, No. 98. Guadalupe Island. Weber-van Bosse (loc. cit.), p. 366. Caulerpa cylindracea Sonders, Alg. Preiss, Botan. Zeit., 1845, p. 49. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALG£ ^29 These were robust plants, whose branches were well clothed with cylindrical ramelli, blunt, but barely swollen at the sum- mit. The type is from western Australia. 28. Caulerpa racemosa var. laetevirens f. typica Weber-van Bosse Mason, No. 122. Guadalupe Island. Weber- van Bosse (loc. cit.). Our plants are robust specimens with fairly closely placed, well inflated ramelli, on long tapering pedicels. The type is from Toud Island, north of Australia. I'^amily Cqdiace.^ CHLORODESMIS H.\rvey and Bailey, Proc. Boston Soc. Nat. Hist., vol. 3, 1851, p. Z7i 29. Chlorodesmis comosa Bailey and Harvey Mason, No. 97, Guadalupe Island, and No. 17, Clarion Island. There was only a single young example in the collec- tion from the lattter localitv. Bailey and Harvey (loc. cit.). The Clarion Island plant was a young example and typical, but the Guadalupe plant seems to represent only a scrappy basal portion. The latter is referred to this species without absolute certainty since the upper portions with typical dicho- tomies are lacking. The type came from Fiji but the plant is abundant in the tropical Pacific, growing usually as a cuma- tophyte, or surge plant. CODIUM Stackhouse, Nereis Brit, Fasc. 2, 1797, p. XVI 30. Codium fragile (Suring.) Hariot Growing on rocks. Mason, No. 7, Guadalupe Island. Hariot, Algues du Cap Horn, 1889, p. 32. Acanthocodium fragile Suringar, Alg. Japon., Index, 1867. No. 7 represents a slender form (or state) of this wide- spread species, \^"e did not detect it in the Gulf of California specimens collected by the California Academy Expedition of 1921 (cf. Proc. Calif. Acad. Sci.. 4 ser.. vol. 12, No. 29, J30 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. 1924). It is of decided interest therefore to find it among the subtropical Guadalupe collections, and not among the tropical collections of the Gulf of California and of Clarion Island. The temperature control of this species as well as of the rela- tions between Guadalupe Island, the ocean coasts of the main- land, and the coasts of the Gulf of California are not at all clear. 31. Codium decorticatum (Woodw.) Howe? Mason, No. 16, Clarion Island. Howe, Phyc. Studies, V, 1911, p. 494. Ulva decorticata Woodward, Trans. Linn. Soc, vol. 3, 1797, p. 55? We refer to this species specimens similar to those we re- ferred under it in our Marine Algae of the Pacific Coast of North America (Part II, 1920, pp. 172-175) and with the same mental reservations. The original plant of Woodward is described as being destitute of a base, terete, branched toward the base, six feet and over in length, and four lines in breadth. The branches were long, once but not over twice branched and compressed at the base of the dichotomies, the apices being attenuate-obtuse. The base of the specimen, being expanded, was probably at or very near the attachment. Near the base it was branched into three or more parts, one of which was very short, two were dichotomously branched about six inches above their origin, continuing simple to their tips, and the fourth or longest, after being divided once near the base, con- tinues simple for three feet, then divides dichotomously, the branches continuing simple to the end. The type presumably came from some one of the Mediterranean coasts, but the exact locality is not definitely known. No type specimen is known, so that the characteristics of the utricle remain in doubt. C. A. Agardh (Spec. Alg., 1822, p. 454) presumed that the Ulva decorticata of Woodward was the same as his Codium elongatum, described as compressed, with the type locality at Cadiz. Montague (Fl. Alger., vol. 1, 1846, p. 49, pi. 13, fig. 1) also describes it as compressed. Of later de- scribed species, two have a nearer approach to the habit of that of Ulva decorticata Woodw. than to the Codium elongatum Ag. One is Codium Chasaliei Weber-van Bosse (Journ. de Bot, vol. 13, 1899, p. 134) from the Cape Verde Islands, over Vol. XIX] SETCHELL AND GARDNER—THE MARINE ALGJE J3J a meter in length, cylindrical, rarely branched, with utricles 3 mm. long, 80 /^ in diameter at the base, enlarging to 250 /* (even to 525 /* in portion of type material kindly sent by Dr. Anna Weber- van Bosse) at the summit, and with a number of sporangia spirally arranged on each. The other is Codiiim Jongiramosiim of Setchell and Gardner (Proc. Calif. Acad. Sci.. vol. 12, 1924, p. 710, pi. 15, f. 27, and pi. 37), from the Gulf of California, over a meter in length, cylindrical, branched chiefly at the base, with the utricles 1-1.8 mm. long, up to 1.2 mm. broad, and sporangia unknown. The latter species seems to be slightly dilated below the axils but no men- tion is made of this in the former. Bornet (Les Algues de P. K.-A. Schousboe, 1892, pp. 216, 217), has described the puz- zling variations of the forms ascribed to Codiunt elongatum in Schousboe's collection, both as to habit and as to character of the utricles and subordinates the degree of infra axillary dilation to the relative size of the utricles, dividing them into (1) those with larger utricles and (2) those with smaller utricles. M. A. Howe, who places all the variants under C odium decorticatum (Woodw.) Howe (Phyc. Studies, V, 1911, pp. 494, 495), states that the utricles of Agardh's type specimen of Codiiiui elongatum are from 110-225 /x in greatest diameter, while the La Paz plants he refers to his C. decorti- catum have utricles up to 520 /x in greatest diameter, reach a length of decidedly over a meter, and are flattened now and then under the dichotomies. Mason's No. 16, from Clarion Island, is a small plant, only 13-14 cm., branched somewhat above the base, with compara- tively long branches for its length. It is cylindrical, but some- what flattened and dilated under the axils. The utricles are 1-1.5 mm. long and up to 650 /a in greatest diameter, tapering from rounded apex to narrow base and thin-walled through- out. The hairs are situated in a circle just below the broad summit and are constricted at the point of connection, sud- denly swollen above this and tapering off above as in C. bul- hopilum Setchell. We are inclined to regard No. 16 as a young sterile plant. Hanna, in his journal of the voyage (Proc. Calif. Acad. Sci., Ser. 4, vol. 15, 1926, p. 37), in speaking of the dredging operations off Sulphur Bay on Clarion Island, says : "These pieces of apparatus brought up enormous quan- 132 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. tides of broken coral, coral sands, and seaweeds. The latter belong chiefly to one species which grows as long slender stalks, round in cross section and bright green in color. The sailors called it 'Spaghetti.' " Mr. Mason informs us that this was a Codiuni and that the material thus dredged in fair depth of water was wrapped with other coarse species, such as Sar- gassums, etc., in a piece of cheesecloth and placed in one of the kegs of alcohol with fish specimens. Unfortunately, this parcel has not been located among the collections of the trip. We suspect that these "Spaghetti" represent older and better developed states of No. 16. which we place under C odium decorticatnni (Woodw.) Howe, with the suspicion that they may possibly be related rather to C. longirmnosiim S. and G. or to C. ainfylk'csicidafuni S. and G. 32. Codium latum Suringar? Dr. A. Palmer, in 1875. collected a broad, flattened Codium on Guadalupe Island which we have referred (Mar. Alg. Pac. Coast N. A., Part 2, 1920, p. 175, pi. 15, f. 6) under the Codium latum of Suringar, being led thereto by the resem- blance of our plant, both in habit and in utricle, to the illus- tration of that species by Okamura (Icones of Japanese Alg;e, vol. 3. 1915. pi. 142, f. 4 and 6). These figures, however, are not entirely in accord with those of Suringar (Algae Jap. Mus. Bot. Lugd. Bot.. 1870. p. 22. pi. 7). especially as to the details of the structure of the utricle. An examination of utricles from the type specimen, for which privilege we are indebted to Dr. Anna Weber-van Bosse, shows the type agreeing with the figures of Suringar rather than with those of Okamura. Sur- ingar does not figure any utricles with the peculiar hair struc- tures shown by Okamura, but his specimen may have been young, or possibly also, he may have selected a specimen where they were not abundant. It may be, although this seems less probable, that there are two or more broad species in Japan. In fact Okamura (Icones of Japanese Algae, vol. 3, 1915, pi. 136, figs. 1, 3, 4. and 7) has figured a broad plant under Codi- um divaricatum Holmes. This plant differs so much from the type as figured by Holmes, and as also figured by Okamura (loc. cit.. fig. 2) as to lead one to suspect that they may be Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALG.^ \^^ specifically distinct. The broad specimen of Okamura (loc. cit., fig. 1) resembles in habit the C. damcBcorne of Kuetzing (Tab. Phyc, vol. 6, 1856, pi. 98), but the utricles are different in shape. The utricles of Okamura's broad C. divaricatum resemble those of Suringar's type of C. laUim in every way except that the apical membrane of Okamura's plant is de- cidedly thickened. The question as to whether there is more than one broad Codium of the general habit of C. latum in Japan is still to be decided. The habit of the Guadalupe plant agrees in general with that of those figured by both Suringar and Okamura for Codium latum but has a greater number of dichotomies and has the lower dichotomies extended to the very bases. The basal branches are also very much more slender below than is repre- sented for the Japanese plant. The utricles of the Guadalupe plant resemble fairly closely those given by Okamura but not so closely those given by Suringar and those examined from Suringar's type specimen. We feel inclined to separate the Guadalupe plant and dedicate it to its collector, but in view of the uncertainty as to the situation among the Japanese species. we retain our previous disposition of it, calling attention to the fact that there is very little in common between the Japa- nese algal flora of warmer waters and those of the similar waters of the west coast of North America. 33. Codium simulans S. and G. Mason, No. 15, Clarion Island, and No. 41, Guadalupe Island (scrap). Setchell and Gardner, Mar. Alg., 1924, p. 706. plate 14, figs. 21, 22, and plate 31. Mason's No. 15 from Clarion Island agrees fairly well with the Gulf of California plants upon which we founded Codium simulans, except that the dimorphism of the utricles seems more pronounced and the larger (balloon-type) of utricle reaches a much greater diameter (up to 325 m) and has the apical wall thin, while the larger utricle of the type is not so strongly set off from the narrower type (very similar in both type and Clarion Island plants) and has its apical wall slightly to decidedly thickened. The Guadalupe plant agrees closely 134 CALIFORNIA ACADEMY OF SCIENCES [Pboc. 4th Seb. with the Clarion Island plant as to utricle characters. The Guadalupe plant is fertile. HALIMEDA Lamouroux, Nouv. Bull. Sci. Soc. Philom., vol. 3, 1812, p. 186 34. Halimeda Opuntia (L.) Lamour. Mason, No. 28, Guadalupe Island. Lamour., Hist. Polyp.. 1816, p. 308. CoraUina Opuntia Linnaeus, Syst. Nat., 1758, p. 805, Sol., Nat. Hist. Zoophyt., 1786, p. 110, pi. 20, fig. 6. The Guadalupe plants seem to belont^ to the typical form of this widely distributed tropical species. Family Phyllosipiionace^ OSTREOBIUM Bornet and Flahault, Sur quelq. pi. viv, dans le teste calc. des. mollusques, 1889, p. 15 35. Ostreobium Reineckei Bornet Abundant in shells and Melobesice. H. L. Mason, Nos. 209, Guadalupe Island, and 217, Clarion Island, etc. Bornet, Engler's Jahrb., vol. 23, 1897, p. 269. The specimens agree very well with the original description and with specimens from Samoa. Although searched for in our decalcifications, nothing pertaining with certainty as to the presence of other tranophytes was discovered. Family Valo.niace-E DICTYOSPHJERIA Decaisne, Essais Class. Alg., 1842, p. 328 36. Dictyosphaeria Versluysi Weber-van Bosse Mason, No. 79, Guadalupe Island. Weber- van Bosse, La Nuova Not., Ser. 16, 1905, p. 142. Our specimens are solid, .<^how segments up to 2 mm. in diameter, with frequent intracellular "cellulose'' spines (or hairs) up to 320 fi in length. They agree with Weber-van Bosse's description, except that both segments and **hairs" have somewhat greater dimensions. "J'he species occurs in the East Indies and in Hawaii. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE 135 SIPHONOCLADUS Schmitz, Ueber griine Algen, 1878 37. Siphonocladus pusilloides sp. nov. Plate 4, figs. 6 and 7 Fronds fasciculate, clavate, 7-10 mm. high, 400-500 /x diam. at the outer end, 90-125 /* diam. at the base; straight or slightly arcuate ; wall very thick and lamellose, smooth, h}-a- line; rhizoids several times branched. Type: No. 173644, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 110), in May, at Guadalupe Island. The specimens under No. 110 are difficult to place and we. at first, assigned them provisionally under Valonia, since they resemble very closely the V. pusilla of Kuetzing's figures (Tab. Phyc, vol. 6, 1856, p. 30, pi. 86, b-e) from the Adriatic. Hauck refers this under Siphonocladus and it may be that our plant is a juvenile condition of some such species as S. tropi- cus, a species of the West Indian region (Lesser Antilles at least), Canary Islands, and the neighborhood of Honolulu. The very early stages of Siphonocladus tropicus, e.g., are claviform and simple (of. Borgesen, Contr. a la conn, du genre Siphonocladus Schmitz, 1905, pp. 260, 261, fig. l,a), and the early stages of 5". pusillus are presumably represented by Kuetzing's figures already cited. In the uncertainty of rela- tionships, it seems best to call attention to this interesting little plant and to assign it a name under the genus Siphonocladus, since its shape and an occasional partition seem to indicate its possible affinities. Family Dasycladace^ ACETABULARIA Lamouroux, Polyp. Flex., 1816, p. 244 38. Acetabularia parvula Solms-Laubach Mason, No. 174, Clarion Island. Solms-Laubach, Monogr. Acetab., 1895, p. 29, pi. 2, figs. 3, 5. A few specimens of a small Acetabularia were detected in the Clarion Island material. The stalk is stout, about 3-4 mm. long, and the disk about 3-4 mm. in diameter. The ray cells number from 14 to 18, are broadly wedge-shaped, gently 136 CALIFORNIA ACADEMY OF SCIENCES [Peoc. 4th Se«. rounded on the outer end or with trace of apiculum, and slightly indented at the partitions. Coronal processes reach 52-65 fi in diameter, each with 3-4 hair scars. There are no aplanospores present. The calcification of the disks is strong only on the contact faces of the rays. This plant agrees fairly closely with the description and figures of Solms for his Acetabtilaria parvula from Macassar in the East Indies. Family Cladophorace.e CHJETOMORPHA Kuetzing, Phyc. Germ., 1845, p. 203 39. Chaetomorpha antennina (Bory) Kuetz. Growing on rocks. Mason, No. 20, Guadalupe Island. Kuetzing, Sp. Alg., 1849, p. 379. Confen'a antennina Bory, Ouatre lies d'Afr., vol. 2, 1804, p. 161. It is difficult to be certain of the habit of this form of ChcB- tomorpha, but it is certainly entangled above, though it appears to be erect below. While we have found filaments tapering to a small fraction of the ordinary diameter above, we have not been able to detect a strictly basal cell. The lowest cell found was 75 /i in diameter and 500 /* long, while the upper cells are 500-550 fi in diameter and up to 2 or even 3 times as long as broad. It may be a form of Ch. antennina of our Pacific Coast of North America and probably widespread in the Pacific Ocean. It approaches also M. A. Howe's Ch. carti- laginea from the Chincha Islands in some of its characters. Until the base is known, the exact determination must remain in doubt. Such characters as are determinable in our specimens indicate possible intermediate position between Bory's species and that of Howe. MICKODICTYON Decasne, PI. de I'Arab. in Arch, du Mus. II, 1841, p. 115 40. Microdictyon Palmeri Setchell. Guadalupe Island. Setchell. Univ. Calif. Pub., Bot., vol. 13. p. 106, 1925. We have seen a single specimen in Herb. Farlow, collected by Dr. E. Palmer in 1875. It belongs to the Virescentes sec- tion of the Calodictyon group and has elongated cells in the primary filaments. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE i;^y Family Ulvace^ ENTEROMORPHA Link, Epistola, 1820, p. 5 41. Enteromorpha plumosa Kuetz. Growing on rocks among other alg?e. Mason, No. 31, Clarion Island. Kuetzing, Phyc. Gen., 1843, p. 300, pi. 20, fig. 1. The plants referred here from Clarion Island are in agree- ment with our idea of this species as expressed in part II of our Marine Algae of the Pacific Coast of North America (1920, p. 259). 42. Enteromorpha lingulata J. Ag. Mason, No. 81, Guadalupe Island. J. G. Agardh, Till. Alg. Syst, 1885, VI. It seems best to refer to this species, specimens which occur having much the habit of Enteromorpha compressa, but with the cells more regularly arranged in vertical rows than is cus- tomary in that species. ULVA LiNN^us, Gen. Plant, 1737, p. 326 43. Ulva angusta S. and G. var. ? A single narrow frond. Mason, No. 45. Guadalupe Island. The absence of a base makes the reference of this Ulva un- certain, but its cell structure recalls that of U. angtista rathei than that of U. Linsa. The cells are rounded quadrate to polygonal in surface view, sections through the fronds are 60 /a and more thick, and the cells 25-30 /* in every diameter, the cells being practically square in cross section. It may possibly be a form of U. Lactuca but it differs decidedly in habit as well as in thickness from that species. It may be only a robust form of our U. angusta known hitherto only from central California. 44. Ulva rigida Ag. Cast ashore ? Mason, No. 99, Maria Madre Island. Agardh, Sp. Alg., vol. 1, part 2, 1822, p. 410. 138 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. The fronds are broader than long and without finger-like lobes. The fronds are 80-85 /* thick, with the cells of each layer higher than broad. 45. Ulva Lactuca L. Mason, No. 120, Clarion Island. Linnaeus. Sp. Plant., vol. 2, 1753. p. 1163. The membranes of our plants are somewhat perforated, but otherwise they resemble closely the Ulva Lactuca of Vickers's Algae Barbadenses (Plate 1), which is Ulva Lactuca in the sense of Thuret and a widespread tropical type. Family Ch.etophorace;e ULVELLA Crouan, Notes sur qiielq. nouv. algiies mar., 1859, p. 288, pi. 22, fig, E 46. Ulvella Lens Crouan Growing on various species of algae. Mason, Nos. 180, 181, Guadalupe Island. Crouan (loc. cit.). This seems close to the plant we have credited to the Cali- fornia coast in our Marine Algae of the Pacific Coast of North America (part II, 1920. p. 295, pi. 33). The central cells are empty, having presumably discharged their zoospores. MELANOPHYCE^ Family Sphacelariace;e SPHACELARIA Lyngbye, Hydrophyt. Dan., 1819, p. 103 47. Sphacelaria furcigera Kuetz. Growing on Sargassum Palmeri. Mason, No. 90. South Anchorage, Guadalupe Island. Kuetzing, Tab. Phyc, vol. 5, 1855, p. 27, pi. 90, fig. II. The base is more or less endophytic, penetrating the host. The main filament is 45 /* in diameter and the propagula are slender and bifurcate. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALG^ \y^ 4?>. Eisenia (?) Masonii sp. nov. Plate 14, fig. 44 Stipe and holdfast unknown; blade (?) bearing numerous, complanate, bipinnately branched sporophylls 3-5 dm. long, with considerably thickened rhachis and membranaceous pin- nae and pinnules beset along the margins with numerous sharp teeth with broad bases; pinn?e stipitate in the lower parts of the rhachis, pinnules mostly not stipitate ; sori on the rhachis 146 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4Tn Ser. and at the base of the stipitate pinnules, not extensive ; unilo- cular sporangia intermingled with unicellular paraphyses pro- vided with hyaline appendages at their tips. Brought up from deep water with the ship's anchor. Type: No. 173700, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 5), in April, at Guadalupe Island. There were two sets of fragments, this number and the next, which came to the surface during the hoisting of the anchor. This species was provided with scanty sori whose sporangia and paraphyses were clearly of a Laminar ioid type. We can only suspect that these fragments may repre- sent portions of the lateral sporophylls of some Alarioid genus similar to Eiscnia. 64. Eisenia (?) desmarestioides sp. nov. Plate 15, fig. 45 Stipe and holdfast unknown; blade (?) giving rise to nu- merous complanate, bipinnately branched sporophylls up to 4 dm. long, with much thickened rhachis and numerous alter- nate pinnx and pinnules with deeply serrated margins ; pinnae and pinnules linear, stipitate finely bullate over their entire surface ; reproduction unknown. Brought up from deep water on the ship's anchor. Type: No. 173701, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 6), in May, at Guadalupe Island. Very similar to the last in general characters and obtained in the same way. The single specimen is narrow and the sur- face bullate. It recalls Carpoglossum qucrcifoJhim (Turn.) J. Ag. (cf. Harvey, Phyc. Austr., vol. 1, pi. 43, 1858) in outline but is thinner and Laminarioid rather than Fucoid. We sus- pect it to be part of a sporophyll of some such genus as Eisenia, although the specimen is sterile. No such degree of branching is known among the sporophylls of any Eisenia, but a suggestion is to be found in those of Eisenia bicyclis (Kjellm.) Setchell and E. cava (Kjellm.) Okam. (cf. Kjell- man, in Engler and Prantl, Die Naturl. Pfl.-fam., I Teil. Abth. 2, p. 245, p. 166, B, and Vega. Exp. Vetensk. Jakt.. Bd. IV, Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE J 47 pi. 10. 1885). Eisenia arborea Aresch., the only species on the west coast of North America has usually simple sporophylls as has also E. Cokcri Howe from the coast of Peru. The Japa- nese species of Eisenia and Eclclonio are to be considered, but no one of them has such extremely compound sporophylls as the two sets of specimens before us. Family Cutleriace^ AGLAOZONIA Zanardini Saggio, 1843, p. 10 65. Aglaozonia canariensis Sau\ . Mason, No. 176. Clarion Island. Sauvageau, Observ. sur quelq. Dictyotace^, 1905. Resembling sterile plants of Zonaria variegata (Lamour. ) Ag., but the differences between the dorsal and ventral epi- demis and the scattered moniliform rhizoids lead us to suggest the possibility of being near to, if not identical with, the Aglaononia canariensis of Sauvageau, a species originally de- scribed from the Canary Islands but apparently occurring throughout the West Indies. It is a very different plant from the A. pacifica Setchell. from 1'ahiti. Family Dictyotace^ DICTYOTA Lamouroux, Nouv. Bull. Soc. Philom., vol. 1, 1809, p. 331 66. Dictyota cribrosa sp. nov. Plate 11, fig. 40 Fronds light brown, perforated irregularly, narrow below, expanding upwards, flabellately divided above the middle, the branches appearing as lobes at the summit, over 8 cm. long (basal portions wanting). 4-5 mm. broad below. 2-5 cm. across the llabellate expansions, 6-7 mm. diam. in upper divi- sions; all divisions cuneate, thin and fragile, 85-110 /j- thick, middle cells clear; margins ciliate-dentate, teeth 1 mm. long, slender, scattered, more or less re^rularlv. with scattered hair clusters and broadly oblong oogonia in subcircular sori ; an- theridia and aplanospores unknown; surface cells elongated. 4-5 to each central cell. Cast ashore. J48 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Type: No. 173683, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 3), in May, at Guadalupe Island. The present species resembles most nearly Dictyota creniilata J. \g., but differs from that species as we have interpreted it (Mar. Alg. C/ulf. Calif., 1925, p. 730, pi. 18, figs. 50. 51) in being somewhat taller and broader, more flabellately branched above, in being somewhat thinner (D. crcnulata is 130 /a and over thick) and having the central layer of cells clear instead of colored. 67. Dictyota Masonii sp. nov. Fronds 4-7 cm. high, 2-3 mm. wide, dichotomo-pinnate, slightly stupose at the base; segments linear, with smooth mar- gins below and rounded but narrow angles; distance between main branches 4-6 mm. ; apices mostly blunt ; surface cells 10-14 /* diam., 2-2> times as long as the diam. : central layer of cells 45-55 /* diam. and about twice as long, with a single group of chromatophores in the center ; marginal cells thickened and meristematic, giving rise to numerous prolifera- tions above but soon falling off and producing new plants ; reproduction unknown. Cast ashore. Type: No. 173614, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 22), in June, at Clarion Island. No. 22 differs from D. dcntata of the West Indies by being broader in habit and lacking acute tips. It lacks the dichoto- mies of D. Bartayresii and P. I'k'csii Howe. The callose margins seem to distinguish it. 68. Dictyota sp. ? Cast ashore. Mason. No. 14, Clarion Island. No. 14 recalls both D. Bartayresii Lamour. and D. pardalis Kuetz., but does not agree with either. The plants are low and sterile, possibly they are )oung. .\ basal transverse sec- tion is aliout 260 ^ thick, the large cells are higher than wide Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE 149 and the outer cells are nearly quadrate. The marginal cells are conspicuous for their deep brown contents. NEUROCARPUS Web. and Mohr, Beitrage zur Naturkunde, vol. 1, 1805, p. 300 69. Neurocarpus dehcatulus (Lamour.) O. Kuntze. Cast ashore. Mason, No. 158. Clarion Island. O. Kuntze, Rev. Gener. plant., 1891, p. 907. Dictyopteris delicatiila Lamouroux. in Nouv. Bull. Philom., 1809, n. 20, pi. 6, fig. B. A small, delicate, sterile plant, seemingly referable here, occurred in small quantity among the Clarion Island collec- tions. It is found in the Atlantic and in the Indian oceans. ZONARIA Ac. (Ihn. mut.), Syn. Alg. Scand., 1817, p. XX 70. Zonaria Farlowii S. and G. Cast ashore at Guadalupe Island, Mason, No. 4. Setchell and Gardner, Mar. Alg. Pac. Coast, Part III, 1925, p. 660, pi. 34, fig. 5, pi. 36, fig. 20, pi. 43, fig. 63, and pi. 97. The plants referred to this species are slender and ragged, even naked below. They bear oogonia and their attendant paraphy.ses. PA DIN A Adanson, Fam. II, 1763, p. 30 71. Padina tetrastromatica Ilauck? Piate 8, fig. 41 Cast ashore. Mason, No. 100, Maria Madre Island, Mexico. Hauck, in Hedwigia. 1887, p. 43. Our specimens bear antheridia which occur in a zone on each side of a zone of hairs. About the middle, the frond consists of 6 layers of cells. As to indusium, there seems to be none, but none of the antheridia is as yet sufficiently mature to show dehiscence. Seemingly a somewhat thicker plant than those of either Hauck or \\"eber-van Bosse. It is a species of the Indian Ocean. J !^Q CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. 72. Padina Durvillei Bory. Cast ashore. Mason. No. 101. Maria Madre Island, Mexico. Bory, in Diet. Class. Hist. Nat, vol. 12, 1827, p. 591. Our specimens are thick and dark-colored even in alcoholic specimens. The inner layers of cells number 6 to 8, with the colored surface lavers. Thev are sterile, with irreerular con- centric zones of dark hairs. The type is from Chile. Family Sargassace^ BLASSEVILLEA Decaisne, Sur Thallas., 1840, p. 409 73. Blossevillea Brandegeei S. and G. A sinj^le fragment, cast ashore. Mason, No. 2. Guada- lupe Island. Setchell and Gardner, in Gardner. Nuclear Ex- trusion, 1910, p. 127, pi. 16, figs. 8-10. Only a fragment of this species, described from and limited, so far as is known, to Guadalupe Island, was found in the col- lections. There are a few conceptacles but nothing of a basal portion. SARGASSUM Agardh, Sp. Alg., vol. 1, 1820, p. 1 74. Sargassum Palmeri Grunow Cast ashore. Mason, Nos. 1, 25, 85, and 92. Guadalupe Island. Grunow. Add. cog. Sargass., 1915, p. 338. Typical plants of this Guadalupe species were collected. Thev show both oosronia and antheridia. It was first collected by Dr. Edward Palmer in 1875 and later by T. S. Brandegee. It occurs floating and possibly attached as far north as Santa Cruz (A. Grunow!). 75. Sargassum paniculatum J, Ag. Guadalupe Island. Dr. Edward Palmer, 1875. J. G. Agardh. Sp. Alg.. I, 1848, p. 315. There are specimens in Herb. Univ. California and Herb. Farlow, determined by Major Th. Reinbold. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGM \C^\ RHODOPHYCE.-E Family Bangiace^ GONIOTRICHUM Kuetzing, Phyc. Gen., 1843, p. 244 76. Goniotrichum Alsidii (Zan.) Howe Epj phytic on various algcC. Guadalupe Island, Mason, No. 154, and scattered specimens in various other collections. Howe, Mar. Alg. Peru, 1914, p. 75. Bangia Alsidii Zanar- dini, Bibl. Ital., vol. 96, 1839, p. 136. Filaments forking at an angle of about 45°, 10-12 /jl in diameter, with cells in a single row, occurred in various prepa- rations. They seem to belong to this species as usually under- stood. Family Gelidiace^ GELIDJUM Lamouroux, Essai, 1813, p. 41 (Repr.) 77. Gelidium microphysa sp. nov. Plate 9, fig. 31 Fronds compressed throughout, 1-1.5 cm. high, main axis up to 1.25 mm. diam., flabellately branched, with branches numer- ous and short ; apical cell in a conspicuous notch ; cystocarpic ramuli spatulate, constricted at the base ; surface cells spherical. 4-5 ft diam. ; rhizoidal filaments abundant, fairly evenly dis- tributed in the subcortex and medulla ; tetraspores and antheri- dia unknown. Growing on rocks. Type: No. 173635, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 121), in April, at Guadalupe Island. The specimens are short and broad, resembling most nearly Gelidium microptenun Kuetz. (Tab. Phyc, vol. 18, p. 21, pi. 59, figs, e-g, 1868) in habit, terminal cell sunk in a broad shallow notch, and the position of the cystocarp. G. microp- terum is credited to Cape Colony and has been referred to G. cartilagineiim by J. G. Agardh with a query. We have not seen a specimen of Kuetzing's species and since ours is shorter, broader, and far removed in locality, feel inclined to bestow upon it a provisional name until its identity may be more clearlv established. It is difficult for us to associate either our 152 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. specimens or those of Kuetzing with the very different G. car- tilagineum. The species is named inicrophysa because of the minuteness of the superficial cells. Family Gigartinace^je AHNFELDTIA Fries, F1. Scan., 1835, p. 310 ' 78. Ahnfeldtia gigartinoides J. Ag. Growing on rocks, Clarion Island, Mason, No. ?>2). J. Agardh. Nya Alg., 1847, p. 12. The Clarion Island plants are the low, scrubby, irregularly branched plants of the type illustrated by Kuetzing (Tab. Phyc, vol. 19, 1869, p. 26, pi. 71a-e) rather than the sym- metrically branched dichotomous plants of the Hawaiian A. concinna J. Ag. We suspect, however, that the two species may be identical. The type locality is St. Augustine, western coast of Mexico, where it was collected by Liebman. Kuetzing's figures are of Liebman's plants. MYCHODEA Hooker and Har\-ey. in London Journ., vol. 6, 1847, p. 407 79. Mychodea episcopalis J. Ag. (?) A few fragments among other algce, cast ashore at Guada- lupe Island. Mason, No. 167. J. Agardh. Till. Alg. Syst., VII, 1885, p. 82. The only complete specimen is a dwarf (or dwarfed) plant about 3 cm. long. It has the same structure as the type speci- men and the cystocarp of the Gigartinace.ne. It is not only smaller than the type of Mychodea episcopalis J. Ag., but it shows no coiled tips. It may be an undescribed species related to M. pnsilla (Harv. ) J. Ag., but in that species the cysto- carps are subterminal, while in ours they are well below the terminal region. Family Sph.erococcace^ GRACILARIA Greville. Alg. Brit., 1830, p. 121 80. Gracilaria crispata S. and (i. f. ( ?) Growing on rocks. Mason, No. 178. Clarion Island. Setchell and Gardner. New. Mar. Alg., 1924. p. 7^2-^, pi. 22. figs. 7-10. and pi. 44. a. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE J 53 The fronds are clustered, very little over 1 cm. high, attenu- ated into a flattened stipe below, expanding into a flabellate, palmate expansion above, whose divisions are irregularly crisped or lacerate. The structure, as well as the habit in miniature, suggests close relationship to the Gulf of California species. Family Rhodymeniace.^ CHAMPIA Desveaux, Journ. Bot., vol. 1, 1808, p. 245 81. Champia parvula (Ag.) Harv. A few fragments cast ashore among minute algse. Clarion Island. Mason, No. 74. Harvey, Ner. Bor. Amer., part 2, 1853. p. 76. Chondria parvula Agardh, Syst. Alg., 1824, p. 207. Only fragments occur in the Clarion Island collection. The filaments are up to 600 /* in diameter. The tetrasporangia are tripartite and scattered. It seems to belong to this species attributed to the Atlantic Ocean, the Mediterranean Sea, the East Indies, and Japan. HOOPERIA J. Agardh, Anal. Algol., cont. 3, 1896, p. 89 82. Hooperia Baileyana (Harv.) J. Ag. A few small specimens, on Eel Grass. Mason, No. 72, and on Sargassum sp., No. 91, South Anchorage, Guadalupe Island. J. G. Agardh (loc. cit), p. 90. Chylodadia Baileyana Harvey, Ner. Bor. Amer., part 2, 1853, p. 185, pi. XX, C. What seems to be this fairly common species of East Atlan- tic United States and the West Indies, occurs in the Clarion Island material. No. 72 is typically tetrasporic while No. 91 shows antheridia covering the entire surface of the large por- tion of the upper part of the branchlets. Family Hypneace.e HYPNEA Lamouroux, Essai, 1813, p. 43 83. Hypnea Evermannii sp. nov. Fronds densely branched, having 3-5 orders of branches, rigid and somewhat cartilaginous; primary branches mainly J 54 CALIFORNIA ACADEMY OF SCIENCES [Peoc. 4th Ser. Standing at right angles to the more or less contorted main axis, 3-4 cm. long, these in turn branching subdichotomously ; main axis and ramuli densely clothed with perpendicular, ulti- mate fructiferous ramuli, these occasionally forked, with acute apices and not constricted at the base; antheridia in rather extensive, somewhat swollen sori at or near the base of the fructiferous ramuli; cystocarps and tetraspores unknown. Cast ashore. Type: No. 173625, Herb. Calif. Acad. Sci., collected by H. L. Mason (no. 21), in April, at South Anchorage, Guada- lupe Island. Unfortunately only a fragment of an antheridial plant of this seemingly distinct species of Hypnea was collected, hence a complete diagnosis of the species is not possible at this time. It seems close to H. MarchantcB S. and G. and H. Johnstoni S. and G., both from the Gulf of California, and to the Red Sea H. Valentice (Turn.) Mont., but the spinulose ramellae are mostly simple in H. Evermannii and only occasionally forked. Family BONNEMAISONIACE.q£ ASPARAGOPSIS Montagne, in Webb and Berthelot, Phyt. Caiiar., vol. 3, part 3, 1840, p. XV 84. Asparagopsis Sanfordiana Harv. Cast ashore. Clarion Island, Mason, No. 13. Harvey, in Trans. Royal Irish Acad., vol. 22, part 5, 1855, p. 544. Our plants seem to be closer to the typical form than to the f. amplissinui S. and G. of the Gulf of California. P'amily Rhouomelace/E RICARDIA Derb. et Sol., in Derbes, Ann. Sci. Nat. Bot., 4 Ser.. vol. 5, 1856, p. 211, pi. 14 85. Ricardia Montagnei f. gigantea Farlow Growing on Laurencia Masonii. Guadalupe Island, Mason, No. 132. Farlow, in Farlow, Anderson, and Eaton, Alg. Exsicc. Am.-Bor., No. 58, 1878 (nomcn nudum ). Vol. XIX] SETCHELL AND GARDNER—THE MARINE ALG^ 155 Only a few small specimens were encountered, growing on the tips of Laurencia Masonii. The smallest plants bearing tetrasporangia reached only 0.5 mm. in height, while the Cali- fornian plants, as a rule, are much larger than those described for the type of the species. The variety is therefore of doubt- ful status. Kylin (Entwick. Florid., 1928, p. 94-102) has recently resurrected for this species the specific name saccata of J, G. Agardh (Oefvers. Act. Holm, 1849, p. 89), which, however, is a manuscript name applied by Greville to a Calif ornian plant seemingly under the impression that the plant in question belonged to the Dumontia saccata of his synopsis (Alg. Britt. Syn., p. Ixii, 1830), which in turn was founded on the Fuciis saccatus Turn. (Fuci, pi. 241). Greville, seemingly, intended to refer the plant described by J. G. Agardh to what we now call Halosaccion fncicola (or H. glandif orme ) , but J. G. Agardh, while taking Greville's name, recognized the generic difference between Greville's plant and Turner's. J. G. Agardh also, seemingly confirming Greville's use of the name, later (1876, p. 369) renamed the species Erythrocystis Grevillei, thus disposing of any suspicion that he considered himself responsible for the specific name "saccata." It is, in our esti- mation, a questionable application of the priority rule to select the specific name "saccata" in preference to the long established "Montagnei" conferrerl by Derbes and Sober in 1856 (!oc. cit.). LAURENCIA Lamouroux, Essai, 1813, p. 43 86. Laurencia Masonii sp. nov. Fronds 12-20 cm. high, repeatedly and profusely branched, with branches of 6-8 orders, widely divaricate and each re- duced in size; main axes up to 3.5 mm. diam. ; fructiferous ramuli very abundant, clavate, constricted slightly at the base, more or less fasciculately branched ; superficial cells thin- walled, pentagonal or hexagonal, 25-30 /x diam.. sliglitly longer than broad in the main branches, shorter than broad at the apices of the ramuli; large medullary cells with much thickened walls on one-half of the cell, the thickening crescent- shaped in cross section; fascicles of hair filaments included 156 CALIFORNIA ACADEMY OF SCIENCES [Pkoc. 4th Ser. within the apical pits; tetrasporangia 90-120 ft diam. ; antheri- clia and carpogonia unknown. Cast ashore and growing on Sargassiim Palmeri. Type: No. 173698, Herb. Calif. Acad. Sci., collected by H. L. Mason (no. 8), in April, at South Anchorage, Guada- lupe Island. The proposed new species described above seems to come nearest to Laurencia heteroclada Harvey of West Australia. It belongs to the Filiformes section of the genus but does not show the heteromorphy of Harvey's plant. It resembles the more prominently branched forms of L. Forsteri (Mert.) Grev., but is even more frequently branched, with branchlets more attenuate at their bases. 87. Laurencia humilis sp. nov. Plate 9, figs. 32 and 33 Fronds diminutive, 8-15 mm. high, 1-2 mm. diam., very sparsely branched ; medullary cell without crescent-shaped thickenings of the walls ; surface cells quite variable in shape and size, mainly subcircular in surface view, up to 30 yu, diam. ; subcortical cells very much larger; chromatophores parietal, forming a network of crooked rods; tetrasporangia crowded at the outer ends of the filaments ; cystocarps unknown ; antheridia in dense, grapelike, much branched clusters, each branchlet terminated by a large spherical cell. Growing on rocks. Type: No. 173627, Herb. Calif. Acad. Sci., collected by H. J. Mason (No. 175), in April, at Clarion Island. This dwarf (or dwarfed) species seems distinct from any described, being nearest, perhaps, to L. nana M. A. Howe of the West Indies. It is stouter than that species and its branch- lets are shorter and more stubby and it has the epidermal cells more circular to elliptical in surface view than in L. nana. The chromatophores are parietal, slender and crooked, forming a regular but labyrinthine figure lining the cell wall (see plate 9, fig. 33). While it may be only a low form or state of some other species, it seems mature, since the specimens show both tetraspores and antheridia. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE 157 88. Laurencia papillosa var. pacifica S. and G. Growing on rocks. Guadalupe Island, Mason, No. 1 19. Setchell and Gardner, Mar. Alg. Gulf Calif., 1924, p. 765, pi. 23, Hg. 18 ; pi. 24, fig. 33 ; pi. 43a-b, and pi. 54. The specimens referred under this tropical species agree with the varietal type in all essential characters. The cortical cells are more rounded, 12-25 /* in greatest diameter (often the horizontal diameter) and the tetrasporangial ramelli are broad turbinate with a single ring (constant?) of tetrasporan- gia at the top. 89. Laurencia sp. nov.? Plate 8, fig. 30 Fronds prostrate, attached by short, broad disks, giving rise on the opposite side to numerous short, unbranched, clavate filaments; erect filaments similar to fructiferous ramuli in other species of Laurencia and with the surface cells sub- spherical, 25-30 /I diam., projecting, giving the surface a finely tuberculate appearance ; prostrate filaments and apices of the erect filaments 230-300 fi diam. : erect filaments up to 2 mm. diam. ; reproduction unknown. Cast ashore, probably growing on rocks among various other small algae. Mason, No. 165, Guadalupe Island. Only a small fragment of this most interesting and, so far as the incomplete fragment shows, most distinct plant is avail- able. The prostrate stem is 7.5 mm. long, cylindrical, about 230 /x thick, with smooth epidermis and with the walls of the intermediate cells strongly thickened, the thickenings often locally placed and often just below an erect branch or near a fascicle of rhizoids. It is attached to the substratum by fas- cicles of rhizoids. The erect branches are cylindrical, about 1.5 mm. long, slightly and gradually attenuate at the base. The cortical cells of the erect branches project, giving them a distinctly papillose appearance. The fragment is sterile. Several species, seemingly of the same general habit, have been described and figured by Kuetzing in the fifteenth volume of the Tabulae Phycologicse. They are Laurencia perforata Mont. (pi. 49, e-g), from the Canary Islands, L. radicans Kuetz. (pi. 50, d-e) from the Adriatic Sea, and L. vaga Kuetz. December 30, 1930 158 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. (pi. 50, a-c), and L. decitmbens Kuetz. (pi. 51, a, b) from New Caledonia. L. microcladia Kuetz. has a creeping base and thickenings of the walls of the intermediate cells, but is not papillose, while L. gemmifcra has papillose cortical cells but no thickenings of the walls of the intermediate cells. It seems unwise to name and attempt to describe our plant from a fragment showing so little of the habit, but we call attention to its peculiarities in the hope that it may occur again in more complete form. JANCZ'EWSKIA Solms-Laubach, Note sur le Jancsewskia, etc., 1877 90. Janczewskia Solmsii Setch. and Guern. Parasitic on Laurencia Masonii. Guadalupe Island, Mason. No. 93. Setchell and Guernsey, in Setchell, Parasitic Floride.ie, I. 1914, p. 9, pi. 2, figs. 7, 8; pi. 3, figs. 17-19, pi. 5, figs. 26, 27. While our plant agrees too closely with Jancsewskia Solmsii to be separated from it and shows tetrasporangia, antheridia. and cystocarps, the cystocarpic conceptacles are broad and there are sterile tips. These last, perhaps, show that the speci- mens are young. CHONDRIA Agardh, Syn. Alg. Scand., 1817, p. XVIII 91. Chondria clarionensis sp. nov. Fronds 2-3 cm. high, nearly 1 mm. diam. at the base, taper- ing to acute apices, rigid ; branches of at least three orders, arising on all sides, widely divaricate; trichoblasts numerous, profusely branched, growing on the acute tip of the branch as well as on the tips of short secondary branchlets, in pits or depressions for some distance back of the apices, then becom- ing decidious; ultimate ramuli constricted at the bases, abruptly tapering to acute apices ; cortical cells in surface view 8-15 /I diam., 2-4 times as long, subcortical layer composed mostly of two layers, larger than the surface cells; medullary cells subspherical, up to 125 /u- diam., colorless, with lenticular thickenings on the walls; antheridia thin, circular disks, 300- 350 M diam. ; cystocarps short stipitate, 0.5-0.75 mm. diam., with broadly pyriform carpospores 200-230 /x long. Cast ashore. Vol. XIX] SETCHELL AND GARDNER—THE MARINE ALGM ^59 Type: No. 173631, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 18) at Clarion Island. The plants referred to this species are very low, yet they bear well developed tetrasporangia, antheridia, and cystocarps. The trichoblasts are on an emergent conical tip, not sunk in a depression. The branchlets are few, inclined towards dis- tichous in arrangement, but all the axes are cylindrical. It is a member of the Euchondria section. It has lenticular thicken- ings of the walls of the medullary cells, short stipitate cysto- carps, straight tips to the branches and branchlets, with cor- tical cells 8-15 jtt by 30-45 /* as to prostoplast and with walls 3-4 fi thick in the antheridial plant. Our species comes nearest to Ch. acrorhisophora S. and G. of the Gulf of California, but has very different cortical cells and shows no tendency towards cirrhate tips. 92. Chondria sp. Growing among other algse. Mason, No. 168. Guadalupe Island. Our plant comes nearest to Chondria tcmiissima, credited with wide range. The habit and tetrasporangia agree with English specimens. The cortical cells agree closely in shape and measurements, the protoplasts averaging 1.5 times as long as broad. There are no lenticular thickenings in the walls of the intermediate cells nor any rhizoidal or circinate appendages at the tips of either branches or branchlets. The chromato- phores appear discoid below and in the form of a broken band near the apex. It comes near to the var. calif ornica Collins but does not agree exactly. It is acute at the tips, resembling Ch. lance olata Harv., is low, generally naked or with few tri- choblasts, and has some tendency toward distichous arrange- ment of branchlets. The bases of the branchlets are not so extremely attenuated as is represented for Ch. lanceolata and we have no exact information concerning the cortical cells or possibility of internal thickenings of walls in that species. It arises from a prostrate rooting basal portion. 160 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th See. POLYSIPHONIA Greville, FI. Edin., 1824, p. 308 93. Polysiphonia tongatensis Harv. var. ( ?) Fronds at least 2.5 cm. high and 130-145 /* diam., flaccid, sparsely branched, with 4 pericentral cells; branches strict, very gradually attenuated upwards, crowned by a group of long, dichotomously branched hairs remaining attached to 20-30 segments back of the apices ; segments about 2 times as long as broad below ; chromatophores discoid ; long unicellu- lar rhizoids arising from the pericentral cells at various levels along the frond ; tetrasporangia more or less discontinuous, arising in the subultimate ramuli, nearly filling the segments, spirally arranged ; cystocarps and antheridia unknown. Cast ashore, entangled among other small algae. Mason (No. 130), South Anchorage, Guadalupe Island. Harvey, in Kuetzing, Tab. Phyc, vol. 14, 1864, p. 14, pi. 41, fig. a-d. We have only a fragment of a tetrasporangial tip, but this agrees well with plants of the central Pacific referred to this species and particularly to var. upoluensis Grun. The base, critical in determination for species of this group of Polysiphonia, is unfortunately lacking. Our frag- ments recall also the figure of Polysiphonia siamensis Martens (Tange, Preuss. Exp. n. Ost. As., 1866, p. 31, pi. 7, fig. 1). In case P. tongatensis Harv. and P. siamensis prove identical, Harvey's name as published by Kuetzing (Tab. Phyc, vol. 14, 1864, p. 14, pi. 41, figs, a-d) has priority. Martens' species, however, is rooting above and is said to have 4-6 pericentral cells. 94. Polysiphonia Masonii sp. nov. Fronds flaccid, attached by a dense fascicle of short, rhizoi- dal filaments terminating in discs, of a reddish-brown color, 2-3 cm. high, 350-400 fi diam. at the base of the main axis, repeatedly and regularly dichotomously branched, with the branches gradually reduced in diameter toward the apices; pericentral cells 4, surrounding a relatively large central fila- ment ; segments less than quadrate below, slightly more than quadrate in the median parts, reduced to one-half or one-third at the apices; ultimate ramuli 140-150 ix diam., abruptly at- Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE \(,\ tenuated at the apices, crowned with fairly numerous, long, dichotomously or trichotomously branched hairs ; tetrasporan- gia spherical, spirally arranged in the ultimate and subulti- mate segments, 85-95 fi diam. ; antheridial clusters moderately abundant, arising on the basal cell of the hairs, broadly and irregularly fusiform, 80-95 /^ diam., terminated by a single small sterile cell ; cystocarps spherical to subspherical, almost sessile, 300-325 ^^■ diam. ; carpospores narrowly pyriform, 100- 125 /x long. Growing on Zostera marina. Type: No. 173618, Herb. CaHf. Acad. Sci., collected by H. L. Mason (No. 86), in April, at Guadalupe Island. P olysiphonia Masonii seems to answer most nearly to the description and figures of P. Blandi Harv. (Phyc. Austr., vol. 4, pi. 184, 1862) as to regularity and dichotomy of frond, but the joints are longer and the ultimate ramelli more slender and gradually attenuate in that species, while in our plant they are more blunt above (when mature) and abruptly contracted below the trichoblast covered short tip. The stichidia in P. Blandi are zig-zag with the tetrasporangia projecting while in our plant they are submerged and the ramuli are smooth. 95. Polysiphonia Eastwoodae sp. nov. Fronds attached by a disk, relatively rigid, moderately branched, 8-11. cm. high, 350-400 fi diam. at the base, with 4 very large pericentral cells surrounding a relatively small cen- tral filament, not corticated, of a dark brownish-red color; branches strict, relatively long, gradually tapering upwards; segments up to 1 mm. long in the lower parts of the main axes, gradually diminishing in length to the apices ; tricho- blasts in small, relatively short tufts at the apices, subdichoto- mously branched; tetrasporangia spherical, arranged spirally in much swollen segments of the ultimate ramuli; 90-110 h- diam. Cystocarps and antheridia unknown. Growing on rocks. Type: No. 173674, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 55), in April, at South Anchorage, Guada- lupe Island. 152 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Named for Miss Alice Eastwood, curator. Department of Botany, California Academy of Sciences. Polysiphonia Eastivoodce belongs to the j^roup of uncorti- cated, 4-siphoned species, with a discoid holdfast and "leaves." In these characters, sinj^ly or in combination, it is excluded from P. tongatensis, P. Olneyi, and P. subtilissinia, and is to be distinguished from P. havanensis, P. mollis, etc., by its not being monopodial in its branching and by the basal attachment. It differs from P. gorgonice Harv. in its shorter segments. %. Polysiphonia homoia sp. no v. Fronds soft and flaccid, sparsely branched, attached to the host by numerous long, contorted, unbranched, monosi- phonous, nonseptate, thick-walled, rhizoidal filaments, 3-6 cm. high, 350-370 ju diam. at the base, with 5 relatively large peri- central cells, but usually 3 at the base of the ramuli ; segments 1.5-2 times as long as broad; primary branches apparently dichotomous below, giving rise to secondary and tertiary branches above; ultimate ramuli very much reduced in length and diameter and usually constricted perceptibly at the base : trichoblasts absent or very sparse, when present very slender and sparsely branched ; tetrasporangia elongated, arranged in a straight series, 110-120 /* diam., nearly occupying the entire length of the segments; antheridia in small conical clusters terminated by 2-3 sterile cells, remaining attached for 20-30 segments back of the apices; 50-60 /* diam., 170-190 /i long; cystocarps immature. Growing on C odium sp. Type: No. 173641, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 35), in April, at Guadalupe Island. Polysiphonia homoia approaches P. variegata (Ag.) Z;i- nard., but is low, uncorticated, more slender, and constantly 5-siphonous. Its habit of being epiphytic on C odium may also be characteristic. 97. Polysiphonia guadalupensis sp. nov. Fronds 3-6 cm. high, 1-1.25 mm. diam. at the base of the largest axes, branching dichotomous, moderately abundant. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGjE 153 with branches widely divaricate, even at times recurved, cor- ticated below ; branches gradually attenuated upAvard, termi- nating in a dense cluster of long, repeatedly and dichotomously branched, very slender trichoblasts ; pericentral cells 5, very large, surrounding the very small central filament one-third to one-half as long as the diam. of the filament; tetrasporangia spirally arranged, extending through two or more orders of ultimate and subultimate ramuli, 75-85 fi diam. ; antheridia in typical clusters at the apices of the fronds, subconical to cylin- drical, 280-320 /A long; cystocarps ovoid, relatively large, on short pedicels, standing almost erect; carpospores relatively large and sparse. Growing on Sargassuin Palmeri. Type: No. 173639, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 24), in April, at Guadalupe Island. The present species is another 5-siphonous plant, more or less corticated towards the robust base, displaying much of the habit of Polysiphonia violacea (Roth.) Grev., but constantly showing 5 instead of 4 pericentral cells. It is more definitely corticated than is usual in P. variegata (Ag.) Zanard, and more rigid and bushy in appearance. FALKENBERGIA Schmitz, in Schmitz and Falkenberg, Rhodomelaceae, in Engler and Prantl., Naturl. Pflanzenfam,, 1897, p. 479 98. Falkenbergia Hillebrandtii (Bornet) Falkenb. Growing on Codium sp. Guadalupe Island, Mason, No. 128. Falkenberg, Rhodomelacese, 1901, p. 689. Polysiphonia Hillebrandtii Bornet, in Ardissone, Phyc. Med., vol. 1, 1883, p. 376. Our specimens are sterile. The diameters of the main fila- ments are about 50 /a. The Guadalupe plants resemble those from the Bermuda and Bahama Islands. As to how distinct F. vagabitnda (Harv.) Falk. and F. rufo-lanosa (Harv.) Schmitz are from each other and from F. Hillebrandtii must remain a question not to be satisfactorily decided apart from abundance of material of the Tasmanian and southwest Aus- tralian plants. 154 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. HERPOSIPHONIA Naegli, in Schleid. und Naeg., Zeits. Wiss. Bot., vol. 3, 1846, p. 238 99. Herposiphonia tenella (Ag.) Ambronn Cast ashore among other algse. Clarion Island, Mason, No. 159. Ambronn, Botan. Zeit., vol. 38, 1880, p. 197, pi. 4, figs. 9, 11, 13, 16. Our single specimen is a fragment which agrees so far as it goes with M. A. Howe's specimens from the Bahama Islands. There is also a slender filament accompanying the one we have assigned to this species which has fewer siphons, which may be a variant or may belong to another species. 100. Herposiphonia rigida var. laxa var. nov. Plants more slender in all their diameters and less rigid than in the species and with the branches of unlimited growth developing only slightly except at irregular intervals. Only tetrasporic plants were found, cast ashore among other small alg?e. Type: No. 173623, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 126), in April, at Guadalupe Island. This seems to be onlv a lax and more slender form than the type of the species. HETEROSIPHONIA Montagne, Prod. Phyc. Pol. Antarct., 1842, p. 4 101. Heterosiphonia subsecundata (Suhr) Falkenberg South Anchorage, Guadalupe Island. Mason, No. 49. Falkenberg, Rhodomelaccc-e, 1901, p. 643, pi. 18, fig. 20. Dasya subseaindata Suhr, in Flora. 1840, p. 280. Both antheridial and sterile plants were collected. They seem to be typical of this species of the western coasts of both North and South America. DASYA Agardh, Syst. Alg., 1824, p. XXXIV 102. Dasya Stanfordiana Farlow A fragment cast ashore among other algc-e, Guadalupe Island, Mason, No. 151. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE J55 Farlow, Algae, hi Robinson, Flora of the Galapagos Islands, 1902, p. 94. Fragments, corticated to the extreme apex, seem to agree with Farlow's description and show a much more compact and corticated plant than Dasya pacifica Harv. when compared with a paratype of Harvey's species. It is a much denser plant than D. arhuscula (Dillw.) Ag. Our scanty specimens show both tetrasporangia and antheridia. 103. Dasya Eastwoodae sp. nov. Main axis alternately branched, both axes and branchlets densely corticated, the axes and especially the branchlets giving rise to numerous, alternately arranged ramuli ; the ramuli monosiphonous, dichotomously branched in all directions, with branches widely divaricate and gently incurved, the older cylindrical throughout, the younger slightly tapering to blunt apices; cells of the mature ramuli 55-60 /u, diam., 1.5-2.5 times as long, with numerous, parietal, more or less crooked and elongated, discoid chromatophores and thick cell walls; stichi- dia ovate-lanceolate in outline, truncate below, gradually taper- ing above, on 2-3 celled pedicels arising as one of the dicho- tomies of the third or fourth order, forming a zone in the middle third of the branchlet region ; antheridia and cystocarps unknown. Cast ashore. Type: No. 173638, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 27), in April, at Guadalupe Island. We possess a fragment only about 2 cm. long but showing the branching and the stichidia. It resembles most closely D. arhuscula (Dillw.) Ag.,. but the ramelli are much more slender. 104. Dasya sp. A sterile fragment of much more slender and less corti- cated species than either of the preceding, was collected at Guadalupe Island. Mason. No. 170. We mention this fragment of an unidentifiable Dasya, simply to call attention to the undoubted existence of a third species of this genus on Guadalupe Island. ]56 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. COLACODASYA Schmitz, in Engler und PrantI, Natiirl. Pflanzenfam., 1897, p. 473 105. Colacodasya sinicola S. and G. Growing parasitically on Chondria clarionetisis sp. nov. Clarion Island, Mason, No. 162. Setchell and Gardner, Mar. Alg. Gulf. Calif., 1924, p. 770. pi. 28, fig. 63. Tetrasporangial, antheridial, and cystocarpic plants were detected on Chondria clarionensis. They agree better with C. sinicola S. and G., on Chondria acrorhi::ophora in the Gulf of California, than C. verruccpfonnis Setchell and McFadden on the coast of California proper. Family Ceramiace^e RHODOCHORTON (Naeg.) Emend K. M. Drew, Rev. Gen. Chantrausia, Rhodochorton, and Acrochcetium, 1928. Nsegli, Ceram., 1861, ]>. 121 106. Rhodochorton Eastwoodae sp. nov. Plate 4, fig. 8 Fronds attached to the host by a single cell, epiphytic, 100- 130 fji high, 1-3 (mostly 2) branches arising from the basal cell ; erect branches sparsely and alternately branched, usually dichotomous at the top of the first cell, 5-7 fi diam. at the base, tapering very gradually to the apex, terminating in a very slender hair; cells 2-4 times as long as broad, with band- shaped chromatophore without pyrenoids; basal cell 8.5-9.5 m diam. ; monosporangia sessile on the lower cells of the frond. 6-7 fi wide. 9-10 fi long; other forms of reproduction unknown. Growing on Dictyota Masonii sp. nov. Type: No. 173637, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 23), in June, at Clarion Island. 107. Rhodochorton Daviesii (Dilhv.) Drew Growing on various species of algie, e. g.. Mason, Nos. 82, 83. 84, 88, 154, 191, etc., Guadalupe Island. Drew (loc. cit.), p. 172. Confcrva-Daviesii Dillwyn, Brit. Confervse. Introduction 1809, p. 72>, Supplement, pi. F. Vol. XIX] S ETC HELL AND GARDNER— THE MARINE ALGJE J 57 SPYRIDIA Harvev, in Hooker, Br. Fl., vol. 2, 1833, p. 336 108. Spyridia filamentosa (Wulf.) Harv. Floating among other algse. Guadalupe Island, Mason, No. 80. Harvey (loc. cit.), p. 337. Fucus filament osus Wulfen, Crypt. Aquat., 1803, p. 64. A sterile plant belonging to this species, at least in the broader sense. CROUANIA J. Agardh, Alg. Med., 1842, p. 83 109. Crouania attenuata (Bonn.) J. Ag. ( ?) A fragment cast up among other algae, South Anchorage. Guadalupe Island. Mason, No. 127. J. Agardh (loc. cit.). Batrachospermum attenuatum Bonne- maison, in Agardh, Syst. Alg., 1824, p. 51, as a synonym under Mesogloia attenuata. The plant referred to this species is a mere scrap, together with an occasional young plant, but they seem to indicate the presence of this species in the eastern Pacific, completing, as it were, its circuit of the warmer seas of the globe. CALLITHAMNION Lyngbye, Hydr. Dan., 1819, p. 123 110. Callithamnion byssoides Arn. Growing on Eel Grass, Guadalupe Island, Mason, No. 89. Arnott, in Hooker, Brit. Flora, vol. 2, part 1, 1833, p. 342. Tetrasporangial, antheridial, and cystocarpic fragments occur in our collections, but no traces of "seirospores." Our plants seem to agree in all essential respects with those described by Borgesen (Algae Dan. W. I., vol. 2, pp. 218-220, figs. 205-207, 1917) from the West Incjies. It has not been reported previ- ously for the Pacific so far as we are aware. GYMNOTHAMNION J. Agardh, Analecta Algol., 1892, p. 27 111. Gymnothamnion elegans (Schousb.) J. Ag. Growing on rocks among other minute algae. Mason, No. 32, Clarion Island. J. Agardh (loc. cit.). CaUithamnion elegans Schousboe, in Agardh, Sp. Alg., vol. 2. 1828, p. 162. 1^ CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. We have only tetrasporanji^ial material, but that seems characteristic, althoiij^h confusion with Ptilothamnion Phima (Dillw.) Thuret is possible. The species has been known hitherto from the Mediterranean and the West Indian areas. ANTITHAMNION N^geli. Neue Algcnsyst., 1847, p. 200 112. Antithamnion sp. A few frajj^ments among other diminutive alga;. Mason. No. 153. Guadalupe Island. Our fragments appear to belong to the "repentes" section, with, however, only a few rhizoidal outgrowths to show this. They seem to belong to low plants, with opposite ramelli, whose basal cell is spherical and conspicuous for both its shape and its deep color. The ramelli are branched, the branchlets being long and nearly second, giving the appearance of a nearly flat-topped (pseudo-) dichotomy. Bladder cells are adaxial from the basal cell of a 2-celled branchlet. It seems nearest to Antithainnion antUlanim Borg., but the branching of the ramelli is not clearly alternately bipinnate. These notes will serve to call attention to it. GRIFFITHSIA Agardh, Syn. Alg. Scand., 1817, p. 281 113. Griffithsia sp. A few fragments cast ashore among other small algse. Mason, No. 53, South Anchorage. Guadalupe Island. We mention the existence of the indeterminable fragments of a member of this genus merely to call attention to its occur- rence on Guadalupe Island. PLEONOSPORIUM N^geli, Ceram., 1861, p. (105) 342 114. Pleonosporium sacchoriza sp. nov. Plate 10, fig. 39 Fronds monosiphonous. uncorticated. consisting of an ex- tensive, branched, creeping portion attached by numerous rhi- zoids from below penetrating the host, and of erect fronds arising from the creeping portion : erect fronds 2-3 mm. high, subdichotomously branched, 26-30 /x diam. at the ba.se, taper- Vol. XIX] S ETC HELL AND GARDNER— THE MARINE ALGM J 59 ing but very slightly to the blunt apices; cells 8-12 times as long as the diam. rhizoids prolonged, single cells 300-500 m long, very much swollen in the middle, terminating in an irregularly saccate swelling; polysporangia sparse, 2-3 arising on short branches in the lower parts of the frond, single above, spherical to slightly elongated, on 1 -celled pedicels, 75-85 H- diam., with approximately 32 spores, and with thick cell-walls; cystocarps and antheridia unknown. Growing on C odium sp. Type: No. 173630, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 37), in April, at Guadalupe Island. We place this plant under Pleonosporiiim because of the general habit and the occurrence of polyspores in the tetra- sporangium. It is distinguished because of its saccate rhizoids penetrating among the utricles of its host. CERAMIUM Ac, Syn. Alg. Scand., 1817, pp. XXVI and 60 115, Ceramium Evermannii sp. nov. Plate 8, figs. 28 and 29 Fronds 4-6 cm. high, flaccid, 390-410 /i diam. in the basal region ; main branches dichotomous, arising by longitudinal splitting of the apical cell, with numerous proliferous branches of limited growth arising from the large nodal cells ; apices forcipate and much incurved; cells of the axial filament 1.5-2 times as long as broad below, slightly swollen at the lower end; corticating bands at the nodes wide, covering about three-fourths of the internode below, almost completely cover- ing them in the ultimate ramuli ; the corticating bands asym- metrical with respect to the nodes, considerably more than half being below and composed of close-fitting, approximately isodiametric cells, forming about four fairly well defined whorls, while the upper part of the band is composed of cells much elongated vertically and without definite arrangement into whorls ; trichoblasts long, numerous, bulbose at the apices when young; tetrasporangia immersed within the band, aris- ing on all sides, 55-65 /x diam. ; cystocarps and antheridia unknown. Among other small alg?e. 170 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Type: No. 173621, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 82), in April, at Guadalupe Island. This seems to be a very distinct species of the group, having the corticating band limited and truncate below and less defi- nite in extending well over the internode above and with the lower internodes lageniform. It is related to C. fruticiilosum Kuetz. and to C. corticiilatum Kylin. 116. Ceramium transversale Collins and Hervey Plate 7, figs. 23 and 24 Growing on Eel Grass, Guadalupe Island, Mason, No. 155. Collins and Hervey, Algse Bermuda, 1917, p. 145. Our plant is somewhat more slender than the plant of Col- lins and Hervey, with the corticating band more delicate, but the details of cell arrangement at the nodes and the tetra- sporangia associate it with this species. The type is from Bermuda (Phyc. Bor.-Am., No. 2049). It occurs also in the West Indies and has been collected on the coast of southern California (Phyc. Bor.-Am., No. 2150). Our plant resembles more closely the Bermuda plants than those of southern Cali- fornia. 117. Ceramium clarionensis sp. nov. Plate 7, figs. 26 and 27 Creeping fronds attached by long, slender, more or less branched, multicellular rhizoids; erect fronds short, 2-4 mm. high, 175-190 /n diam. at the base, regularly and dichoto- mously branched, with circinate-forcipate apices; cells of central filament slightly longer than broad at the base, dimin- ishing in length gradually upward; nodal cells composed of a single band of large cells in the center of the band, cutting off above and below a single band of smaller cells, each of these in part and in turn giving rise to a small angular cell from the side, upper cells of the band giving rise to a whorl of stiff trichoblasts 30-35 /i. long, terminated by a spherical cell : chromatophores in the nodal cells parietal and discoid, those in the axial filament very slender, 2-3.5 /u. diam., mostly simple, extending from the ends and meeting in the equatorial region : Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGM \yi tetrasporangia 65-75 m diam., protruding, usually three at each node on the abaxial side of the filament, the tetraspores in each sporangium subtended by one or two short bracteate fila- ments growing within the sporangial wall; antheridia numer- ous, surrounding the nodes, 1.5 /* diam.; cystocarps borne in the axils of the dichotomies, naked, variously lobed. Growing on Codium simulans. Type: No. 173620, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 75), in June, at Clarion Island. This is a species of the Stenogonia section of Ceramium, apparently approaching C. australe Sonder, but the tetra- sporangia in our plant are not on the older " genicida," are 65-75 /i in diameter, and the geniculum at bearing is about 200 /*, whereas J. G. Agardh states (Anal. Algol., Cont. II, 1894, p. 16) that the tetrasporangia nearly equal the diameter of the geniculum in C. australe. 118. Ceramium personatum sp. nov. Plate 6, figs. 21 and 22 Fronds 8-15 mm. high, attached by a small base, 110-120 m diam. in the lower parts ; segments two times as long as broad in the lower parts, diminishing gradually toward the apices ; branching dichotomous, with only slightly incurved apices ; nodal bands narrow, slightly wider in the lower segment than in the upper, very slightly projecting beyond the internodal cells, with smooth, even margins above and below, larger cells below and smaller cells above the center, some of the large cells of the nodal bands in the lower, older parts of the frond giving rise to descending appendages within the internodal cells; tetrasporangia projecting on the abaxial side of the several dichotomies, 1-2 at a node, without bracteate fila- ments, elongated, somewhat stipitate. and asymmetrical, 75- 85 Ai long ; cystocarps and antheridia unknown. Growing on other algae. Type: No. 173622, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 83), in April, at Guadalupe Island. The primary tetraspores in our specimen are about one quarter to one half immersed, but the secondary are fully J 72 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. naked and short pedicellate. There is some agreement be- tween the Guadalupe specimens and those we described from the Gulf of California under the name of C. caudatuin, but the shape of the internodal cells, the more simple type of cor- ticating band, and the somewhat less "caudate" tetrasporangia seem to indicate the necessity of keeping them distinct from one another. 119., Ceramium afiine sp. nov. Fronds 8-12 mm. high. 30-38 /* diam. at the base, not taper- ing perceptibly except 2-3 nodes at the apices, dichotomously branched throughout, free from proliferating branches, at- tached by penetrating, unbranched rhizoids from the lower prostrate portion, forked apices straight to slightly incurved ; internodal cells cylindrical, with short-conical ends, 30-38 /^ diam. below, 24-28 /a above, 4-6 times as long as broad ; cor- ticating bands narrow, composed of 2-3 rows of rounded cells. the larger cells below the upper smaller ones cut off from these; antheridia in whorls on the terminal and subterminal ramuli, arising from all of the nodal cells; cystocarps and tetraspores unknown. Growing on Codiiim simulans S. and G. Type: No. 173642, Herb. Calif. Acad. Sci., collected by H. L. Mason (No. 36), in April, at Guadalupe Island. At first sight, this species seems to resemble Ceramium fas- tigiatitm var. flaccidiim H. E. Petersen of the West Indies, but the lower cells of the Guadalupe plant are neither so long nor so wide as in the West Indian and the tetrasporangia are com- pletely naked with bracteoid filaments below them. The corti- cating bands in ours are more regular. It seems best to sepa- rate it from the West Indian variety and also from the type of C. fastigiatum as now generally limited. 120. Ceramium ornatum sp. nov. Fronds approximately 4 cm. high, the main axes approxi- mately 130 /A diam., sparsely and dichotomously branched, with occasional proliferous ramuli and all tapering gradually toward the apices, slightly swollen at the nodes; cells of the Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALG^ J 73 axial filament cylindrical, 1-1.5 times as long as broad; nodal band extending beyond the surface of the axial filament, rela- tively narrow, equally distributed above and below the node, composed of one whorl of deep-seated, large cells cutting off above and below usually one whorl each of smaller, more or less globular cells, these in turn giving rise to numerous, small, angular, surface cells, irregularly placed and giving rise to numerous, long, narrow, 4-5 fi diam., trichoblasts ; tetrasporan- gia beginning to form near the base of the main filament and extending throughout the entire system of branches to the ulti- mate ramuli, scattered more or less all the way around the fila- ment at the nodes but mostly in two groups on opposite sides of the filament, naked, projecting upward from the upper half of the band, not subtended by bracteate filaments, 60-65 m wide, 80-90 fj. long; cystocarps and antheridia unknown. Growing on Eel Grass, cast ashore. Type: No. 173632, Herb. CaHf. Acad. Sci., collected by H. L. Mason (No. 191), in April, at Guadalupe Island. A much more robust plant than either C. caudatiim S. and G. from the Gulf of California or C. personatum described in this account. The cortical bands are much more complex and the three species form a small group of the Acrogonia closely related to C. gracillimum Harv. and C. penicillatum Aresch. but differ from them essentially in their completely naked and more or less pedicellate tetrasporangia. 121. Ceramium sp. nov. ? Plate 7, fig. 25 A Ceramium, apparently of the C. strictum assemblage, but lacking cystocarps, antheridia, and tetrasporangia, occurred in an admixture from Guadalupe Island (Mason, no. 127). The drawing (plate 7, fig. 25) shows well the structure, except that the abundant long hairs of the upper nodes are not represented. The older internodes are 230-239 /* in diameter and are slightly longer than broad. The corticating bands are soon narrow and well separated from one another, showing a me- dian, but irregular row of large cells with 2 to 3 layers of outer smaller cells. There are present in each corticating band December 30, 1930 174 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th See. a number of deeply colored cells which grow outward through the cuticular covering. They may be suspected of being mono- spores, since their contents are granular, but possibly they may be trichome structures, either young or of arrested devel- opment. We have not previously observed any such structures in any species of Ceramium. Since the material is scanty and sterile, it does not seem desirable to give the plant a name, but content ourselves with calling attention to its peculiarities. Intermingled with other filamentous algae under no. 127. Mason, no. 169. Guadalupe Island. Family Nemastomace^ 122. Clarionea gen. nov. Fronds very soft, gelatinous, difTorm, of seemingly central mass approaching globular or obpyriform with cylindrical, possibly once or twice dichotomously lobed projections; cen- tral jell}^ traversed loosely by slender branched filaments giving rise toward the surface to an anticlinal layer of loosely placed, short, dichotomously branched, moniliform filaments; cystocarps in the cortical layer occupying a pyriform jelly- lined cavity, consisting of gonimolobes arising from a central group of small cells and surrounded by bracteoid filaments ; carpogonia not seen ; auxiliary cells intercalary dolioform, be- tween two or three cells, each of which gives rise to crowded short bracteoid filaments; conjugating tubes (?) slender, seemingly fusing with the auxiliary cells, after which the auxiliary cell buds off a short rounded cell giving rise to the compact gonimolobes ; antheridia and tetrasporangia unknown. 123. Clarionea Masonii sp. nov. Plate 9, figs. 34 to 38 Cystocarps about 85 /a in diameter, compact, rounded angu- lar, indistinctly 4 or 5 lobed. Pinkish, softly gelatinous algae growing on a crustaceous coralline. Type: No. 173640, Herb. Calif. Acad. Sci., collected by H. L, Mason (No. 30), in June, at Clarion Island. \'0L. XIX] SETCHELL AND GARDNER— THE MARINE ALG^ J75 Clarionea occurred to us in the form of a single rather shapeless mass of jelly, originally of a light red color (teste Mr. Mason), extremely and softly gelatinous, in fact almost mucilaginous. The details of structure were difficult of de- termination and an exact idea of the habit (specimens pre- served in dilute alcohol) was impossible. It seems to belong to an undescribed genus of the Nemastomaceae, near to Plato ma, but the bracteoid filaments of the cystocarps separate it from that genus as well as from any other of the family. The thallus also seems to be different in habit. Family Squamariace^ PEYSSONELLIA Decaisne, PI. Arab., 1841, p. 168 124. Peyssonellia rubra (Grev.) J. Ag, Covering coralline nodules. Mason. Nos. 210, 232, North- east Anchorage, Guadalupe Island. J. Agardh, Sp. Alg., vol. 2, 1851, p. 502. Zonaria rubra Greville, in Linn. Trans., vol. 15, 1827, p. 340, pi. 3, fig. 3. The material, while abundant, is mostly sterile but the tetra- sporangial specimens show it to be of this widespread species. While the plants of the East Indies lack rhizoids (cf. Weber- van Bosse, Siboga Exp., Mon. 59b, 1921, p. 271, fig. 89) and differ in this way from the plant of Europe, our specimens and those we have collected elsewhere in the Pacific Ocean show abundance of them. Family Corallinace^ CHOREONEMA Schmitz, Syst. ueber Florid, 1889, p. 455 125. Choreonema Thureti (Born.) Schmitz Growing parasitically on Corallina cubcnsis (?). Mason, No. 184, Guadalupe Island, April. Schmitz (loc. cit.). Melohesia Thureti Bornet, in Thuret and Bornet, Etud. Phyc, 1878, p. 96, pi. 50, figs. 1-8. Testrasporangial, antheridial, and cystocarpic specimens were found in this interesting parasite, first detected in the Atlantic-Mediterranean region, but now known to extend well over the Pacific Ocean (Australia, Polynesia, Japan). 176 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. FOSLIELLA M. A. Howe, in Britton and Millspaugh, Bahaman Fl., 1920, p. 587 126. Fosliella paschalis (Lemoine) comb. nov. Forming whitish or pinkish circular or irregular thin crusts on leaves of Zostera ( ?) and of larger algae. H. L. Mason, No. 50, on the sporophylls of Eisenia (?), Guadalupe Island; No. 93, on Laiirencia Masonii, Guadalupe Island; No. 192, on Zostera ( ?). Melohesia paschalis Lemoine, Corallinaceae in Borgesen Mar. Alg. Easter Island, 1920. p. 289, fig. 32, f, g. M. A. Howe (1920, p. 587) has called attention to the fact, hitherto overlooked or disregarded, that Lamouroux first de- scribed the genus Melohesia in 1812 (p. 186) and selected as species belonging to it the Corallina memhranacea Esper, Melohesia verritcata, and M. orbicularis Lamouroux. So far as we are aware, the last species was never described and the first two are identical. The genus Melohesia, therefore, was founded on M. memhranacea Lamour. and has soriform con- ceptacles. It is identical as to type species with the genus Epilithon Heydrich. For the species with true conceptacles with a single large central and one-layered thallus. Howe established a new generic name, Fosliella. It seems best to adopt this name, although it may at some time seem desirable, since the type species is Melohesia farinosa Lamour., to restrict it to those having heterocysted thalli. Of such, there are at present only two described species, Fosliella farinosa (La- mour.) M. A. Howe and F. paschalis (Lemoine) comb. nov. The latter is to be distinguished from the former by its smaller tetrasporangial conceptacles (112-160 fi in horizontal diame- ter). The plants of Melohesia farinosa of the Pacific Ocean, including the f. maurifiaiia Foslie, are probably to be referred to F. paschalis. LITHOLEPIS Foslie, New Lithe. 1905, p. 5 127. Litholepis accola Foslie Forming superposed crusts with Peyssonellia rnhra over Lithothanmion validmn Foslie and f. crassiusciihim Foslie. H. L. Mason, No. 28A, Guadalupe Island; No. 210, Clarion Island. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE lyj Foslie, Algol. Notiser, III, 1907, p. 22. ^^ We have quoted only two numbers, although superposed /Ov^^Q'ol^;vX<^ crusts are frequent in our material, because in each of these /Q: j^ ^^ two numbers conceptacles (empty) are present. Our speci-f *^' mens agree with the conception of Lemoine (in Borgesen, ^^,\ Marine Algae of Easter Island, p. 289). The species is proba- bly widespread in the tropical Pacific area. LITHOPORELLA Foslie, Algol. Notiser, VI, 1909, p. 58 128. Lithoporella pacifica (Heydr.) Foslie Forming superposed thin crusts with Peyssonellia rubra over Lithothamnium validum f. crassiusculum Foslie. H. L. Mason, Nos. 219, 225, 229, Clarion Island. Foslie, (loc. cit.), p. 59; Melobesia paciUca Heydrich, Lith. Mus. Paris, 1901, p. 529. This species resembles the last in having its thin crusts superposed, but differs in having vertically elongated cells and huge conceptacles. It is a question as to whether Lithoporella, which resembles more closely Mastophora and Litholepis, which resembles more closely the non-heterocysted species of Fosliella, may be kept separate or may better be united. Un- fortunately, our specimens are sterile and are assigned only provisionally to L. pacifica. LITHOTHAMNIUM Phil., in Wiegm., Arch., vol. 1, 1837, p. 387 (^lim. mtit.) 129. Lithothamnium validum Foslie Very abundant in collections from a few fathoms in the form of nodular calcareous pebbles. H. L. Mason, Nos. 201, 202, 205, 208, Guadalupe Island; Nos. 210 to 232, Clarion Island. Foslie, Algol. Notiser, II, 1906, p. 10. Forming thinner or thicker expansions, either flat or building up nodules up to 3-5 cm. in longer diameter. There is great variation in thickness, character of surface, branching, etc., indicating either great variety in age or development or pos- sibly in specific or varietal segregation. The thinnest crusts resemble Lithothamnium simulans Foslie, the thicker ones usually have short knob-like projections and these pass over oa*/ «»-^h- Ji \yg CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. into erect branching forms. When growing in nodular free thalli, the crusts are often rugose-nodose. Possibly there are two species awaiting detection and segregation, the type of L. validum, restricted to the branching form, and the f. cras- siusculum (Foslie), restricted to the rugose-nodose form. We hope later to be able to throw more light on these variants through a study of the forms of the Calif ornian coast. AMPHIROA Lamouroux, Nouv. Bull. Sci. Soc. Philom., vol. 3, 1812, p. 186 130. Amphiroa fragilissima (L.) Lamour. A few slender fronds with lateral conceptacles, seemingly cystocarpic. H. L. Mason, No. 67, Guadalupe Island. Lamouroux, Hist, polyp, coral, flex., 1816, p. 298. Corallina fragilissima Linn?eus, Syst. Nat., Ed. 12, vol. 1, 1767, p. 1305. A slender variety, 286-428 yu. in thickness, with joints very slightly swollen and with truncate, barely convex tips. It is not typical of the species but seems nearest to it of any described. Since the preceding paragraph was written Mme. Lemoine (Arch, du Mus. d'hist. nat., ser. 6, vol. 4, pp. 78, 79, pi. 4, f. 1, 1929) has described an Amphiroa onuulata from the Gala- pagos Islands. In microscopic structure, particularly in the fairly regular alternation of 3 transverse rows of long cells with 1 row of short cells, in the central axis, and in the very slightly, if at all, swollen extremities of the internodes, the Guadalupe plant is in agreement with A. annulata, but it does not show annulation nor branching so irregular as Lemoine's species which resembles A. anastomosans W.-v. Bosse in these respects. We feel it wise to retain our speci- mens under A. fragilissima, using the name in broad sense, until careful study may indicate the extent of influence of ex- ternal changes of environment on modifying the characters brought forward for separation. CORALLINA Linn;ens, Syst. Nat, 1758 (ed. 10), p. 805 131. Corallina cubensis (Mont.) Kuetz. In tufts, on other algae. H. L. Mason, No. 12, Guadalupe Island. Kuetzing, Tab. Phyc, VIII, 1858, p. 37, pi. 77 ; Jania cubensis Mont, in Kuetzing, Spec. Alg., 1849. p. 709. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGJE J 79 Our plants very closely resemble Kuetzing's figures c, e, and f of plate 77 oi volume 8 of the Tabulae Phycologicse. They differ decidedly in detail from the figures of Borgesen (1917, figs. 174-178) and from the plants distributed by M. A. Howe from the Bahama Islands, but may represent a more sparsely pinnulated form. Mason's plants do not decrease so suddenly in passing from the main axes to the pinnules as do the plants of Borgesen and Howe. Borgesen (Ibid, p. 187 et seq.) has discussed the type specimen and the admixture with JoJiia adhccrens. 132. Corallina subulata Solander On BlosseviUea Brandegcci. Guadalupe Island, T. S. Brau- degee. Solander, Nat. Hist. Zooph., 1786, p. 119, pi. 21, fig. B, b. There are so many difiiculties in the way of determining exactly the specimens collected by Mr. Brandegee that they must be left in considerable doubt. They resemble closely the Solander figures of Corallina subulata. On the other hand, our specimens approach forms usually referred to C. Ciivieri, especially the form figured by Kuetzing (1858, pi. 74) under C. pilifera. JANIA Lamour., Nouv. Bull, des Sci., Soc. Philomat, vol. 3, 1812, p. 186 133. Jania rubens (L.) Lamour. Epiphytic on various algcC. H. L. Mason, No. 182. Guada- lupe Island. Lamouroux (loc. cit. p. 186). Corallina rubens Linnaeus, Syst. Nat, Ed. 10, vol. 1. 1758, p. 806. The main joints are 36^40 n* in diameter, cylindrical. 4-5 times as long as broad, with several nodes and internodes between branches. Our plants seem to be a variety of this widespread species. 134. Jania adhaerens Lamour. On various alg?e. H. L. Mason. No. 185. Guadalupe Island. Lamouroux, Hist, des Polyp. Coral, flex.. 1816, p. 270. The main joints are about 135 /x broad, tapering towards the base, 1 or 2 to an internode, up to about 10 times as long as broad. The axils are broad and the braiKhes divaricate. A very common species in the warmer oceans. ]gQ CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. BIBLIOGRAPHY Adanson, M. 1763. Families des plantes. Paris. Agardh, C A. 1817. Synopsis algarum Scandinaviae, adjecta dispositione universalis algarum. Lund. 1822. Species Algarum rite cognitse cum synonymis, difFerentiis specificis et descriptionibus succinctis. Vol. 1, part II, pp. 169-531. 1828. Ibid., vol. II, part I, pp. I-LXXVI and 1-189. 1824. Systema Algarum. Lund. Agardh, J. G. 1842. Algae maris Mediterranei et Adriatici, observationes in diag- nosin specierum et dispositionem generum. Paris. 1847. Nya Alger fran Mexico. Qifversigt af Kongl. Vet.-Akad. Forh. Arg. 4, no. 1. Stockholm. (Often quoted as "Alg. Lieb."). 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Gomont, M. 1890. Essai de classification des Nostocacees homocystees. Journ. de Hot., vol. 4, p. 349-357. 1892. Monographic des Oscillariees. (Nostocacees Homocystees). Ann. des Sci. Nat., 7 ser., Bot., vol. 15, pt. 1, p. 263-368, pi. 6-14; vol. 16, pt. 2, p. 91-264, pi. 1-7. 1893. Ibid. Reprint p. 1-302, plates and figures same as original. Goodenough, S., and T. J. Woodward. 1797. Observations on the British Fuci, with particular descriptions of each species. Trans. Linn. Soc, vol. 3, pp. 84-235, pis. 16-19. London. Greville, R. K. 1824. Flora Edinensis. Edinburg. 1827. Some account of a collection of cryptogamic plants from the Ionian Islands. Trajis. Linn. Soc, vol. 15, pp. 335-348, pi. 3. 1830. Algae Brittanicae, or descriptions of the marine and other inar- ticulated plants of the British Islands, belonging to the order Algae, with plates illustrative of the genera. Edinburg. Grunow, A. 1867. Reise der ostreichischen Fregatte Novara. Botanischer Theil, vol. 1, Die Algen. Vienna. (The botany of the expedition was published in parts by different people at different times. The whole volume bears the imprint "1870." The first edition of the algae was published in 1867. Hence the discrepancies in citations.) 1915. Additamenta ad cognitionem Sargassorum. K. K. Zoolog.- Botan. Gesell. Verhandl., vol. 66, pp. 1-48, 136-185. Vienna. 234 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Hanna, G. D. 1926. General Report. Expedition to the Revillagigcdo Islands, Mexico, in 1925. Proc. Calif. Acad. Sci., Ser. 4, vol. 15, no. 1, pp. 1-113, text figs. 1-7, pi. 1-10. Hariot, P. 1889. Algues, in Mission scientifique du Cap Horn, 1882, 1883, vol. 5, Botanique, pp. 1-109, pi. 1-9. Paris. Harvey, W. H. 1833. In Hooker, English Flora, vol. 5, part 1. London. 1852-1858. Nereis Boreali-Americana. 1852. Part 1, Melanospermeae. 1853. Part 2, Rhodospermeae. 1858. Part 3, Chlorospermeae. 1855. Some account of the marine botany of the colony of western Australia. Trans. R. I. Acad., vol. 22, part 1, pp. 525-566. 1858-1863. Phycologia Australica. London. 1858. Vol. 1, 1859, vol. 2, 1860 vol. 3, 1862 vol. 4, 1863 vol. 5. Harvey, W. H., and J. W. Bailey. 1851. Descriptions of seventeen new species of alga;, collected by the United States Exploring Expeditions. Proc. Boston Soc. Nat. Hist., vol. 3, pp. 370-373. Hauck, F. 1887. Ueber einige von J. M. Hildebrandt im Rothen Meere und Indischen Ocean gesamelte Algen. Hedwigia, vol. 26, pp. 41-45. Heydrich, F. 1901. Die Lithothamnien des Museum d'histoire Naturelle in Paris, Engler's Jahrb., vol. 28, 1901, pp. 529-545, pi. 11. Hooker, J. D., and W. H. Harvey. 1847. Algae Tasmanicae : being a catalogue of species of algae col- lected by Ronald Gunn, Esq., Dr. Jeannerett, Mrs. Smith, Dr. Lyall, and Dr. J. D. Hooker. Lond. Journ. Bot., vol. 6, pp. 397-417. Howe, M. A. 1911. Phycological Studies, V. Some marine algae of Lower Cali- fornia, Mexico. Bull. Torr. Bot. Club, vol. 38, pp. 489-514, pis. 27-34. 1914. The marine algae of Peru. Mem. Torr. Bot. Qub, vol. 15, pp. 1-185, pi. 1-66. 1920. Algae in Britton and Millspaugh, The Bahaman Flora, pp. 553-618. Hudson, William. 1778. Flora Auglica (ed. 2). London. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALGM J §5 Jurgens, G. H. B. 1816-1822. Algae aquaticae quas in littore maris dynastiam Javeranam et Friseam orientale alluentis rejectas et in harum terrarum aquis habitantes collegit etc. Decades I-XX. Jever. Kirchner, O. 1898. Schizophyceae, m Engler and Prantl, Die NatiJrl. Pflanzenfam., 1 Th., 1 Abt., 177 Lief. Kjellman, F. R. 1893. Laminariacese, in Engler und Prantl, Die Natiirl. Pflanzenfam., I Teil, Abt. 2. Kuetzing, F. T. 1843. Phycologia generalis, oder Anatomic, Physiologic und Sjstem- kunde der Tange. Leipzig. 1845. Phycologia germanica d. i. Deutschlands Algen in biindigen Beschreibungen, nebst einer Anleitung zum Untcrsuchen und Bestimmen dieser Gewachse fiir Anfanger. Nordhausen. 1849. Species Algarum. 1845-1871. Tabulae Phycologicae. Vols. 1-20 and index. Kuntzc, O. 1891-1898. Revisio generum plantarum vascularium omnium atquc cellularium multarum secundum leges nomenclatur?e intcr- nationales cum cnumeratione plantarum exoticarum in itinere mundi collectarum. Wurzburg. 1891, parts 1 and 2, Algae, part 2, pp. 877-930. 1898, part 3 :2. Kylin, H. 1928. Entwickelungsgeschichtliche Florideenstudieii. Lunds Univ. Arssk., N. F., afd. 2, vol. 24, no. 4. Lamouroux, J. V. F. 1809. Observationes sur la physiologic des algues marines et de- scription de cinq nouveau genres de cette famille. Nouv. Bull. Sci. Soc. Philom., vol. 1, pp. ZZO-ZZZ, pi. 6, fig. 2, A, B, C, D. 1809. Memoire sur la Caulerpes, nouveau genre de la famille des algues marines. Journ. de Bot., vol. 2, pp. 136-146, pi. 6, 7. 1812. Extrait d'un memoire sur la classification des polypiers coral- ligenes non entierement pierreux. Nouv. Bull, des Sci. Soc. Philom., vol. 3, pp. 181-188. (Dec.) 1813. Essai sur les genres de la famille des thalassiophytes non arti- culees. Ann. du Mus. d'hist. Nat. par les professeurs de cet etablisscment, vol. 20, pp. 21-47, 115-139, 267-293, pi. 7-13. Paris. (Usually quoted from the reprint, which is paged successively from 1-84. Plates are numbered the same in both.) 1816. Histoire des Polypiers coralligcnes flexibles, vulgairemenl nom- mcs zoophytes. Caen. 135 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Lemoine, Mme. Paul. 1920. Corallinacea;, in F. Borgesen, Marine Algae of Easter Island, in Carl Skottsberg, The Natural History of Juan Fernandez and Easter Island, vol. 2, pp. 285-293. Liebman, F. "1841. Bemarkninger og Tillag til den danskc Algeflora. Kroyers Tidskrift, p. 492. Copenhagen." Link, H. F. 1820. Epistola de algis aquaticis in genera disponendis. Nees, Horae Physicae, p. 1. Linnaeus, C. 1737. Genera plantarum, eorumque characteres naturales secundum numerum, figuram, situm et proportionem omnium fructifica- tonis partium. 1753. Species plantarum, exhibentes plantas rite cognitas, ad genera relatas, cum diflferentiis specificis, nominibus trivialibus, syn- onymis selectis, locis natalibus secundum systema sexuale di- gestas. Vol. 2, Ed. 1. Stockholm. 1755. Flora suecica, exhibens plantas per regnum Suecias crescentes, systematice cum differentiis specierum, synonymis autorum, nominibus incolarum, solo locorum, usu oeconorum, officinalibus pharmacopceorum. Ed. II. Stockholm. 1758. Systema naturae. Ed. 10, vol. 1. 1767. Systema naturae. Ed. 12, vol. I, pars II. Lyngbye, H. C. 1819. Tentamen hyrophytologiae Danicae, contiiiens omnia hydro- phyta cryptogamia Daniae, Holsatiae, Faeroae, Islandiae, Groen- landicC hucusque cognita, systematice disposita, descripta et iconibus illustrata, adjectis simul speciebus Norvegicis. Copenhagen. Martens, G. v. 1866. Die Tange, in Die Preussische Expedition nach Ost-Asien, Bot. Th. Berlin. Meneghini, G. "1837. Conspectus Algologiae Euganeae, germanicis naturatium rerum scrutatoribus Prague anno 1837 convenientibus oblatus. Patavii typ. Minervae. Serorsim imprim. ex Comment di mcnicina del Dr. Spongia, fasc. Sept. 1837." (cf. Pritzel, 1872, p. 212.) 1844. Algarum species novae vel minus notae a Prof. J. Meneghini propositi. Giorn. Bot. Ital. da Filipo Parlatorc, vol. 1, p. 296. Firenze. Vol. XIX] SETCHELL AND GARDNER— THE MARINE ALG.E Jg7 Montagne, J. F. C. 1840. Plantes Cellulaires, in Webb and Berthelot, Histoire naturelle des iles Canaries, phytographia canariensis, plantes cellulaires, vol. 3, part 3. 1842. Prodromus generum specierumque phycearum novarum in itinere ad polum antarcticum. Paris. 1846. Exploration scientifique de I'AIgerie. Algues, vol. 1. Naegeli, C. "1846. Ueber Polysiphonia und Herposiphonia. Zeitschr. f. wiss. Bot., Heft 4, pp. 206-256." 1847. Die neue Algensysteme und versuch zur Begriindung eines eigenen Systems der Algen und Florideen. Zurich. 1861. Beitrage zur Morphologie und Systematik der Ceramiacee. Sitzungsb. der k. b. Akad. Eissen., II, heft III. Munich. Okamura, K. 1915. Icones of Japanese Algae, vol. 3, No. 7, and No. 8. Tokyo. Philippi, Dr. 1837. Beweis dass die Nulliporen Pflanzen sind. Wiegmann's Archiv fiir Naturgeschichte. Jahrg. Ill, vol. 1, pp. 387-393, pi. 9, fig. 2-6. Rabenhorst, L. 1864-1868. Flora Europaea algarum aquae dulcis et submarinae. 1865. Vol. 2. Leipzig. Reinke, J. 1888. Die braunen Algen (Fucaceen und Phaeosporeen) der Kieler Bucht. Bericht. d. Deut. Bot. Gesells, vol. 6, pp. 14-20. 1889-1892. Atlas deutscher Meeresalgen. Berlin. 1889. Part 1. 1892. Part 2. Robinson, B. L. 1902. Flora of the Galapagos Islands. Proc. Amer. Acad. Arts & Sci., vol. 38, pp. 77-269. Washington. Roth, A. G. 1797-1806. Catalecta botanica quibus plantae novae et minus cognitae describuntur atque illustrantur. Leipzig. 1806. Fasc. 3. Sauvageau, C. 1927. Sur la Colpovicnia sinuosa Derb. et Sol. Bull, de la Stat. Biol. D'Arc, vol. 24, pp. 309-353. 188 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Schmitz, F. 1878. Ueher griine Algen aus dem Golf von Athens. Sitzungs. d. Naturf. Gesell. zu Halle, (cf. also Botan. Zeit., 1879, p. 167.) 1889. Systematische Uebersicht der bisher bekannten Gattungen der Florideen. Flora, vol. 72, pp. 435-456, pi. 21. /897. Palkenbergia and Colacodasya, in Schmitz and Falkenberg, Rhodomelaceae, in Engler und Prantl., Die Natiirl. Pflanzen- fam.. 1 Theil, abt. 2, pp. 421-480. Setchcll, W. A. 1914. Parasitic Florideae, I. Univ. Calif. Publ. Bot., vol. 6, no. 1, pp. 1-34. 1923. Ibid, II, vol. 10, no. 6, pp. 393-396. 1924. American Samoa, part 1, The Vegetation of Tutuila Island. Dept. of Marine Biology of the Carnegie Inst, of Wash., vol. 22. Washington, D. C. 1925. Notes on Microdictyon. Univ. Calif. Pub. Bot., vol. 13, pp. 101-107. 1926. Tahitian algae collected by W. A. Setchell, C B. Setchell, and H. E. Parks. Univ. Calif. Publ. Bot., vol. 12, no. 5, pp. 61- 142, pi. 7-22. Setchell, W. A., and N. L. Gardner. 1920. The marine algae of the Pacific Coast of North America. Part II, Chlorophyceae. Univ. Calif. Publ. Bot., vol. 8, pp. 139- 374, pi. 9-33. 1925. Part III, Melanophyce£e. Ibid, pp. 383-898, pi. 34-107. 1924. Phycological Contributions VII. Univ. Calif. Publ. Bot., vol. 13, no. 1, pp. 1-13. 1924. The Marine Algae, in Expedition of the California Academy of Sciences to the Gulf of California in 1921. Proc. Calif. Acad. Sci., Ser. 4, vol. 12, no. 29, pp. 695-949, pis. 12-88. Solandcr, D. 1786. The natural history of many curious and uncommon zoophytes, collected from various parts of the globe by the late John Ellis, etc. Solms-Laubach, le Comte H. de. 1877. Note sur le Jancsewskia, nouvelle floridee parasite du Chondria obtusa. Mem. Soc. Nat. Sci. Natur. de Cherbourg, vol. 21, pp. 209-224, pi. 13. 1895. Monograph of the Acetabulariae. Trans. Linn. Soc, vol. 5, part 1. Sonder, G. 1845. Nova algarum genera et species, quas in itinere ad oras occi- dentalis Novae HoUandiae, collegit L. Preiss, Ph. Dr. Bot. Zeit., pp. 49-57. Vol. XIX] SETCHELL AND GARDNER—THE MARINE ALG^ 139 Stackhouse, J. 1795-1801. Nereis Britannica; continens species omnes Fucorum in insulis Britannicis crescentium. Bath. 1797, fasc. 2, pp. ix-xviii. Suhr, J. N. 1840. Beitrjige zur Algenkunde. Flora, vol. 23, pp. 257-304. Suringar, W. F. R. 1867. Algarum Japonicarum Musei Botanici Lugdimo-Batavi Index prsecursorius. Annales Bot. Musei Bot. L. B. (Sept.) 1868. Ibid. Hedwigia, vol. 7, p. 53. 1870. Algae Japonicae Musei Lugduno-Batavi (edidit societas scienti- arum Hollandica quae Harlemi est). (Cf. also Hedwigia, vol. 9, p. 129.) Thuret, G. 1875. Essai de classification des Nostochinees. Ann. Sci. Nat, 6 Ser. Bot., vol. 1, p. 372. Paris. Thuret, G., and E. Bornet. 1878. Etudes phycologiques. Paris. Turner, D. 1808-1819. Fuci sive plantarum fucorum generi a botanicis ascrip- tarum icones descriptiones et historia. London, 1808, vol. 1 ; 1809, vol. 2; 1811, vol. 3; 1819, vol. 4. Turpin, P. J. F. 1827. Spiruline oscillarioide. In Dictionnaire des sciences naturelles (de Levrault). vol. 50, p. 309. Vickers, Anna. 1908. Phycologia Barbadensis Iconographie des algues marines recoltees a I'ile Barbade (Antilles). (Chlorophycees et Pheo- phycees.) Paris. Watson, S. 1876. On the flora of Guadalupe Island. Proc. Amer. Acad., vol. 11, pp. 105-112. 1876. List of a collection of plants from Guadalupe Island, made by Dr. Edward Palmer, with his notes upon them. Ibid, pp. 112-121. Weber-van Bosse, Anna. 1898. Monographic des Caulerpes. Ann. du Jard. Bot. de Buiten- zorg, vol. 15, pp. 243-401, pi. 20-34. 1899. Note sur quelques algues rapportees par la yacht "Chazalie." Journ. de Bot., vol. 13, pp. 133-135. 1905. Note sur le genre Dictyosphceria Dec. La Nuov. Not., Ser. 16, pp. 142-144. 1913. Liste des Algues du Siboga. I. Myxophycese, Chlorophyceae, Phaeophyceae aves le concours de M. Th. Reinbold. 1921. Ibid, II. Rhodophyceae. Siboga Exp. Monographic LIX b. 190 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser, Weber, R, and D. M. H. Mohr. 1805. Beitriige zur Naturkunde. In Verbindung mit Ihren Freunden verfasst und herausgegeben. Kiel, Akademische Buchhandlung. 1805, vol. 1. Wille, N. 1900. Algologische Notizen, I-VI. Nyt Magazin for Naturvidensk, vol. 38, I. Woodward, T. J. 1797. Observations upon the generic character of Uha, with the descriptions of some new species. Trans. Linn. Soc, vol. 3, pp. 46-58. London. Wulfen, F. X. 1803. Cryptogama aquatica. Roemer's Archiv fiir Botanik, vol. Ill, pp. 1-64. Yamada, Yukio. 1928. Marine Algae of Mutsu Bay and adjacent waters. Sci. Rept. Tohuku Imp. Univ., 4 ser., Biol., vol. 3, pp. 497-534 (with 25 text fig.) Zanardini, G. 1839. Sulle Alghe. Bibliotheca Italiano, vol. 96, p. 131. 1843. Saggio di classificazione naturale delle ficee. Venice. 1858. Plantarum in mari rubro hucuscue collectarum enumeratio. Mem. Roy. Inst. Veneta, part II, vol. 7, p. 297. 1872. Phycearum indicarum pugillus. Mem. Roy. Inst. Venet., vol. 17. jq9 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Sef. Plate 4 Chamcesiphon clavatus sp. nov. Fig. 1. Group of plants, X 250. Phormidium monile sp. nov. Fig. 2. Group of filaments, X 300. Symploca microdonta sp. nov. Fig. 3. Group of filaments, X 250. Calothrix codicola sp. nov. Fig. 4. Group of filaments, X 250. Calothrix clausa sp. nov. Fig. 5. Group of filaments, X 200. Siphonocladus pusilloides sp. nov. Fig. 6. Group of filaments, X 10. Fig. 7. Enlarged tip of filament, X 30. Rhodochorton Eastivooda sp. nov. Fig. 8. Three plants, X 400. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SETCHELL & GARDNER] Plate 4 December 30, 1930 194 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Skr. Plate 5 Sphaci'laria Mason it sp. nov. Fig. y. Filaments and gainetangia, X 300. Strchloiiciiia codicola sp. iiov. Fig. 10. Filaments and gamctangia, X 200. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SETCHELL& GARDNER] Plate 5 J96 CALIFORNIA ACADEMY OF SCIENCES [Proc. -1th Ser. Fig Fig Fig Fig Fig Fig Fig Fig Fig Fig Plate 6 Masoiiopliyciis paradoxa gen. et sp. iu>v. 11. Filament with tctrasporangia, X 250. 12. Filament with gametangia, X 250. 13. Basal filament with erect brancli, X 250. 14. Gamelangium, X 250. 15. Gametangia, the left-hand one empty, X 250. 16. Gametangia, the right-hand one hypertrophicd (?), X 250. 17. Similar to No. 16, X 250. 18. Filament with progula? (or hypertroiihied gametangia?), X 250. 19. Propagulnm (?), X 250. 20. Propagulnm (?), X 250. Ccrainiuiii prrsdiiatii))! sp. nov. Fig. 21. Tip of filament, X 125. Fig. 22. Portion of filament witli tetra.sporangia, X 125. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [ SETCHELL & GARDNER] Plate 6 198 C.ILIFOh'XI.l ACAIU-.MY OF SCIliXCES f Pkdc. 4th Si£R. Plate 7 Ccnuiiutiii Irdiisvrrsalc Collins and liei'vcy Fig. 23. Tip of rtlamcnt, X 250. Fig. 24. Portion of filament with IclrasporanKia, X 250. Crrtiiiiiinn sp. no v.? Fig. 25. Portion of tip of I'llaini'nl showing .yland (?) colls in cortex, X 150. C'l-rdiiiiiiiii clarioiii'iisis sp. nov. Fig. 26. Tip of filament, X 125. Fig. 27. Portion of tilamcnt with tctrasporangia, X 125. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SETCHELL & GARDNER I Plate 7 200 CALIFORNIA ACADEMY OF SCIEXCES IProc. 4th Ser. Plate 8 Ccraiiiiiim Evcrmanuii sp. nov. Fig. 28. Part of upper portion of filament showing hairs and tetraspor- angia, X 125. Fig. 29. Part of lower portion of filament showing swollen nodes and arrangement of cells in cortical hands, X 125. Laurciicia sp. nov.? Fig. 30. Portion of rhizome and branch to show papillate epidermal layer, X 200. PROG. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SETCHELL& GARDNER] Plate 8 K)HftbD 90-) CALIFORXIA AC.IDEMY OF SCII-XCES f Proc. ■< rii Si:r. Pl.ATK 9 (^(•11(1 ill III iiiicnif^liysii sji. iiov. Fig. .11. TTaliil .skelcli. X 3. Laurnicui liiiiiiilis sp. now Fig. 32. ilabil sketcli. X 3. Fig. 33. Cortical cell showing chroniatoi)hores, X 400. Clarioiicd Masaiiii gen. ct sp. nov. Fig. 34. Portion of hranciilct with auxiliary cell, a, and hracctoid fila- ments starting, bl, 1)2, 1)3, X 500. Fig. 35. Similar l)racteoid filaments more advanced. X 500. Fig. 36. Auxiliary cells, a, and glomernles of bracleoid filanunts. I- S^)^). Fig. 37. Auxiliary cell pnlting forth the jirimary oolilastcnia tulie, g, X 500. Fig. 38. Similar to figure 37, with mature cystocarp, c, X 500. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 1 1 |SETCHELL & GARDNER j Plate 9 204 CALIFORXIA ACADEMY OF SCIEXCES [Pkoc. -trn Ser. Plate 10 Plconosl^oriiDii saccurliica sp. nov. Fig. 39. Portion of plant showing creeping tilaniont, saccate rhizoids, branches, and polyspores, X 75. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 1 1 [ SETCHELL & GARDNER] Plate 10 V December 30. 1930 OQ/: CALIFORXI.l ACADEMY OF SCIEXCES [Proc. 4th Skr. Tlatk 11 Dictyota crihrosn sp. nov. Fig. 40. 1 Inlnt <>\ lypo spcciiiK'n. X 1. I'mlina Irtrdslroiittitica Hauck? Fig. 41. Haltit pholof^raph, X 1- PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SETCHELL & GARDNER] Plate 11 Fig. 40 r.g.4l 208 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Plate 12 Desviarestia pacifica S. and G. (?) Fig. 42. Habit photograph, X 1. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 | SETCHELL & GARDNER] Plate 12 210 C.lLIFORM.l ACIDEMY OF SCIHXCES | Pk"C. 4th Sks. Platk 13 Sf'iirdcliiiiis pcdiiiiciilattis (lluds.) Ag. Fig. 4,?. Habit pliotograph, X 1. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 SETCHELL & GARDNER] Plate 13 212 CALIFORNIA .-ACADEMY OF SCIENCES [ I'imc. 4ti. Si k Plate 14 Eisenia (f) Masoiiii sp. nov. Fig. 44. Habit photograph of sporophyll (?), X 1. I PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SETCHELL& GARDNER] Plate 14 Fig. 44 214 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4rH Skr. Plate 15 Eisema (?) dcsmarcslioidcs sp. iiov, Fig. 45. Habit photdt^raph of a .sporopliyll (?), X 1. PROC. CAL. ACAD. SCI., 4th Series, Vol. XIX, No. 11 [SEyCHELL& GARDNER] Plate 15 Fig. 45 PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES ^ ^ ^ Fourth Series /c-S^ t-^oB Lx< A A^ < Vol. XIX, No. 12, pp. 217-397, 134 text figs. January 30, 1931 r^i -^ ^*^ t Lul L I 8 t^ A R \ \^\ -^ XII N'^i^v/^JASS^ PELAGIC MAMMALS FROM THE TEMBLOR FOR- 'JLJ^" MATION OF THE KERN RIVER REGION. CALIFORNIA BY REMINGTON KELLOGG Division of Mammals, United States National Museum This paper presents the results of studies on fossil pelagic mammals from the Temblor formation which outcrops on a hill southwest of Round Mountain, locally known as Shark- tooth Hill, and about seven miles northeast of Bakersfield. four miles east of the Kern River Oil Field, and a quarter of a mile north of Kern River, Kern Countv. California. This hill is located in Sec. 25, T. 28 S., R. 28 E., M. D. M., and is shown but not named on the Caliente sheet of the United States Geological Survey's topographic map. The greater part of the material studied belongs to the California Academy of Sciences and was assembled largely through the active inter- est of Messrs. Paul Shoup and M. E. Lombardi. To. Dr. Barton Warren Exermann and Dr. G. Dallas Hanna, the writer is indebted for permission to study the collection. Prior to the assembling of this collection, several smaller lots, obtained by Mr. Charles Morrice, were presented to the United States National Museum. Detailed descriptions of specimens in both of these collections are herewith given. Through the cooperation of the Carnegie Institution of Wash- ington, arrangements were made for transporting the Academy's collection to Washington, D. C, and that organiza- tion provided additional funds for illustrating the more im- January 30, 1931 218 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. portant specimens. For carrying out the latter purpose, the services of Mr. Sydney Prentice were secured, and he has pre- pared the Hne drawings that accompany this report. Excavations made on Sharktooth Hill in 1924 under the direction of Doctor Hanna and Mr. Morrice, yielded some- thing like a thousand bones, the majority of which were so damaged and imperfectly preserved that they were discarded. Most of the bones are more or less incrusted with a psilomelate of manganese. They occur in a fairly coarse, light gray, firm sandstone, and it is rather surprising that so many of them were broken prior to excavation. No associated skeletons were found, and it would seem that the skeletal elements were disassociated prior to their being covered with the sediments in which they are now found. No satisfactory explanation of the conditions that led to the accumulation of these bones has as yet been set forth. According to Doctor Hanna^ "the bones occupy a stratum not over three feet thick so that the extinction of the excessively abundant species must have occurred in a very short time. The wide extent of the deposit does not indicate that the animals were trapped in a narrow bay as sometimes happens today with whales and sharks." Dr. F. M. Anderson" has suggested that an epoch of violent volcanic activity and fall of ash may have been responsible for the death of large numbers of pelagic animals in the Temblor Sea, but such an explanation does not satisfactorily account for the scattering and mingling of bones of many species of animals. Under such conditions one would expect to find complete, associated skeletons buried in ash and other sediments in the positions in which they perished. Poisonous volcanic gases and inorganic materials may have caused the death of the Temblor animals, but some agency other than volcanic activity must have been responsible for scattering the remains. It is possible that the conditions of deposition at the Sharktooth Hill locality may have paralleled present conditions near Surf, California. The rush of the water at that locality would tear any skeleton apart. Critical study of this collection has led the writer to believe that some of the bones may have decayed before fos- ' G. D. Hanna, Miocene marine vertebrates in Kern County, California. 4 inches and the height as 3 inches. The greatest length of the incomplete Temblor tooth is 72 mm. ; maximum width, 59.5 mm.; height of tooth at level of posterior pillar, 68.5 mm.: and greatest height at level of anterior pair of pillars. 81.3 mm. It is thus apparent that teeth of large size and similar configuration are found in formations varying in age from lower to upper Miocene. The proportions of the adult teeth of the Oregon Desmostylus cymatias are unknown, and. for the present, it seems advisable to refer the Temblor tooth ten- tatively to Desmostylus lies perns. That this tooth (fig. 3) originally consisted of more than five high columns or pillars is shown by the broken border at one end of the base. When the tooth was complete there were at least three pairs of pillars in addition to the single posterior pillar, and one or more at the anterior end. The root is miss- ing, and the exposed smooth surface of the dentine at the base of the crown, as viewed from below, exhibits a general resem- blance to that of a mastodon. Beneath the core of each pillar is a deep conical pulp cavity, and these cavities are separated by a median longitudinal ridge. The end pillar (fig. 2) is somewhat shorter than the others and is closely appressed to the succeeding pair, but all five of these columns are nearly- circular in cross section. The paired pillars curve upward and inward to the median longitudinal axis and have their apices in contact with their opposites. Each of these pillars is covered with a rather thick outer enamel laver which is with difficultv distintjuished from the Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 227 thicker concentric layers of dentine. This tooth is relatively unworn, and hence the crowns of the pillars have a thick enamel rim inclosing a small central pit whose floor is the tip of the central dentine core. The outer surface of the enamel layer is quite rugose. This tooth does not have a distinct cingulum at the base of the crown, but, nevertheless, a small irregular nodosity covered with rugose enamel projects up- ward from the base between each of the pillars. With wear, the circumference of the central pulp cavity increases until in a badly worn tooth the diameter may be thrice the combined thickness of the outer enamel and dentine rings. Order PINNIPEDIA Family ALLODESMID^ Kellogg, new family : Extinct Eared Seals 6. Allodesmus kernensis Kellogg^ Skeletal elements of several individuals, and representing old and young, and possibly both sexes, of this fossil Temblor otariid, are included in the collections made by Charles Mor- rice. The major portion of the material which has been put at the writer's disposal belongs to the California Academy of Sciences, but additional specimens were found in a small col- lection presented several years ago to the United States National Museum by Mr. Morrice. This material adds con- siderably to our knowledge of the morphological history of the Otariidje and especially of the limb structure. After carefully considering all the evidence, the writer is unwilling to propose one or more new names based on doubt- fully distinct bones, yet this disposition of the material is not, however, made without grave misgivings that the reasons for allocating some of the skeletal elements to this fossil pinniped are unsound. There are obvious dififerences in some of the carpal and tarsal elements, particularly in the scapho-lunar, calcaneum, and cuboid bones. In reviewing the skeletal ele- ments it will be observed that the fore and hind limbs do not differ materially from those of living otariids, either in the ' R. Kellogg, Pinnipeds from Miocene and Pleistocene deposits of California. Univ. Calif. Publ., Bull. Dept. Geol. Sci., vol. 13, no. 4, 1922, pp. 26-44. 228 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. proportions of their component parts or in their articular rela- tions. There are minor differences in the vertebral column, but the sternum and pehds exhibit the typical otariid charac- teristics. The mandible is not materially unlike that of the living otariids. but the skull possesses some anomalous fea- tures, of which the backward and outward extension of the premolar-molar series toward the anterior end of the zygoma is probably the most striking. The present material tends to confirm the geological antiquity of the otariid stock, but the source and time of its divergence from terrestrial relatives remain unsettled. The various skeletal elements, which are referred to this pinniped, are herewith listed. Large Individuals — (?) Old Males Left scapula (No. 11857, U. S. N. M.), incomplete. Left humerus (No. 11858, U. S. N. M.), distal end only. Left radius (No. 4292, C. A. S.), distal end missing. Right ulna (No. 4336, C. A. S.), distal epiphysis only. Left ulna (No. 4335, C. A. S.), distal epiphysis missing. Right scapho-lunar (No. 11859, U. S. N. M.), eroded. Right scapho-lunar (No. 4332, C. A. S.), eroded. Left magnum (No. 11860, U. S. N. M.), complete. Left metacarpal I (No. 4466, C. A. S.), proximal end only. Left metacarpal II (No. 4478, C. A. S.), eroded. Right metacarpal II (No. 4481, C A. S.), proximal end only. Left metacarpal V (No. 4480, C. A. S.), proximal end only. Phalanx (No. 4476, C. A. S.), proximal end slightly eroded. Phalanx (No. 4477, C. A. S.), proximal end slightly eroded. Phalanx (No. 4479, C. A. S.), proximal end slightly eroded. Right femur (No. 4294, C. A. S.), complete. Left femur (No. 4295, C. A. S.), internal condyle damaged. Right tibia (No. 4302, C A. S.), both epiphyses missing. Left tibia (No. 4303, C. A. S.), distal epiphysis missing. Left tibia (No. 4494, C. A. S.), distal epiphysis only. Left fibula (No. 4305, C. A. S.), complete. Left patella (No. 4328, C. A. S.), complete. Right patella (No. 4329, C. A. S.), complete. Left patella (No. 11655, U. S. N. M.), complete. Left patella (No. 4326, C. A. S.), complete. Left calcaneum (No. 4309, C. A. S.), complete. Right calcaneum (No. 4310, C. A. S.), tuberosity damaged. Left astragalus (No. 4308, C. A. S.), complete. Left navicular (No. 4321, C A. S.), complete. Left cuboid (No. 4319, C. A. S.), complete. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 229 Right cuboid (No. 4318, C. A. S.), postero-internal angle of distal face missing. Left entocuneiform (No. 4323, C. A. S.), complete. Right entocuneiform (No. 4324, C. A. S.), complete. Left entocuneiform (No. 4322, C. A. S.), complete. Right metatarsal V (No. 11861, U. S. N. M.), proximal end only. Right innominate bone (No. 4360, C. A. S.), distal half missing. Atlas (No. 4398, C. A. S.), nearly complete. Atlas (No. 4414, C. A. S.), incomplete. Fifth cervical (No. 4407, C. A. S.), incomplete. Sixth cervical (No. 4399, C. A. S.), nearly complete. Sixth cervical (No. 4408, C. A. S.), incomplete. First dorsal (No. 4412, C. A. S.), incomplete. Fourth (?) dorsal (No. 4417, C A. S.), incomplete. Fifth (?) dorsal (No. 4416, C. A. S.), incomplete. Posterior dorsal (No. 4421, C. A. S.), incomplete. Sternal segments (Nos. 4403, 4405, 4430, 4404, 4429, 4402, 4428, C. A. S.). Left mandible (No. 4395, C. A. S.), posterior end missing. Right mandible (No. 4426, C. A. S.), incomplete. Left mandible (No. 4486, C. A. S.), both ends missing. ^ Left maxillary fragment with canine (No. 4396, C. A. S.). Right maxillary fragment with canine (No. 4397, C. A. S.). Many teeth (Nos. 4580 to 4596, C A. S.). Individuals of Medium Size — Females or Young Males Right humerus (No. 4337, C. A. S.), proximal epiphysis and distal end missing. Right humerus (No. 4338, C. A. S.), distal end only. Left radius (No. 4293, C. A. S.), proximal end only. Right radius (No. 4291, C. A. S ), proximal end only. Right radius (No. 11863, U. S. N. M.), proximal end only. Right radius (No. 4292, C. A. S.), fairly complete. Right radius (No. 11866, U. S. N. M.), distal end only. Right scapho-lunar (No. 4369, C. A. S.), angle eroded. ^ Right scapho-lunar (No. 4334, C. A. S.), eroded. Right unciform (No. 11862, l). S. N. M.), slightly eroded. Left trapezium (No 4331, C A. S.), complete. Left metacarpal I (No. 4465, C. A. S.), proximal end only. Left metacarpal I (No. 11864, U. S. N. M.), proximal end only Right metacarpal III (No. 4463, C. A. S.), complete. Left metacarpal III (No. 4462, C. A. S.), proximal end only. Left metacarpal III (No. 4459, C. A. S.), complete. Left metacarpal III (No. 4460, C. A. S.), complete. Left metacarpal III (No. 4461, C. A. S.), complete. Right metacarpal IV (No. 4458, C. A. S.), distal end damaged. Right metacarpal V (No. 4451, C. A. S.), slightly eroded. Right metacarpal V (No. 4467, C. A. S.), slightly eroded. 230 CALIFORXIA ACADEMY OF SCIENCES [Proc. 4th Seb. Phalanx (No. 4468, C. A. S.), distal end missing. Phalanx (No. 4469, C A. S.), complete. Phalanx (No. 4470, C. A. S.), slightly eroded. Phalanx (No. 4471, C. A. S.), distal end missing. Phalanx (No. 4472, C. A. S.), complete. Phalanx (No. 4473, C. A. S.), complete. Phalanx (No. 4474, C. A. S.), complete. Phalanx (No. 4475, C. A. S.), complete. Phalanx (No. 4482, C. A. S.), complete. Right femur (No. 4299, C. A. S.), proximal end only. Left femur (No. 4301, C. A. S.), distal end only. Right femur (No. 4298, C. A. S.), distal end only. Right femur (No. 4491, C. A. S.), distal end only. Right femur (No. 4296, C. A. S.), both epiphyses missing. Left femur (No. 4297, C. A. S.), both epiphyses missing. Left tibia (No. 4304, C. A. S.), complete. Right tibia (No. 4492, C. A. S.), proximal end only. Right tibia (No. 4493, C. A. S.), proximal epiphysis only. Right patella (No. 11545, U. S. N. M.). Left patella (No. 4327, C. A. S.). Right patella (No. 4330, C. A. S.). Right patella (No. 4325, C. A. S.). . Right calcaneum (No. 11540. U. S. N. M.), complete. Right calcaneum (No. 11589, U. S. N. M.), complete Right calcaneum (No. 4312, C A. S.), eroded Right calcaneum (No. 4314, C. A. S.), eroded. Left calcaneum (No. 4313, C. A. S.), distal extremity damaged. Left calcaneum (No. 4315, C. A. S.), eroded. Right astragalus (No. 4306, C. A. S.), complete. Left astragalus (No. 4307, C. A. S.), tibial face damaged. Left astragalus (No. 11541, U. S. N. M.), complete. Left astragalus (No. 4311, C A. S.), damaged. Left navicular (No. 11551, U. S. N. M.), complete. Left navicular (No. 11550, U. S. N. M.), complete. Right entocuneiform (No. 11546, U. S. N. ^L), complete. Left cuboid (No. 4317, C. A. S.), eroded. Right cuboid (No. 4316, C. A. S.), complete. Right cuboid (No. 4320, C A. S.), eroded. Left metatarsal II (No. 4452, C. A. S.), proximal end only. Left metatarsal II (No. 4454, C. A. S.), proximal end damaged. Left metatarsal II (No. 4453, C. A. S.), eroded. Right metatarsal II (No. 4456, C. A. S.), incomplete proximal end only. Right metatarsal II (No. 4457, C. A. S.), incomplete proximal end only. Right metatarsal II (No. 4455, C. A. S.), eroded. Left metatarsal III (No. 4450, C. A. S.), distal end missing. Right metatarsal IV (No. 4448, C. A. S.), complete. Left metatarsal IV (No. 4449, C. A. S.), distal end missing. Right metatarsal V (No. 11870, U. S. N. M.), proximal end only. Vol. XIX] KELLOGG— PELAGIC ^L4^L^L-^LS OF KERX RIVER REGION 231 Right metatarsal V (No. 4446, C. A. S.), eroded. Right metatarsal V (No. 4447, C. A. S.), eroded. Atlas (No. 4484, C. A. S.), right and left halves. Third cervical (No. 4409, C. A. S.), incomplete. Fourth cervical (No. 4410, C. A. S.), incomplete. Fifth cervical (No. 4411, C. A. S.), incomplete. First dorsal (No. 4418, C. A. S.), incomplete. Second dorsal (No. 4419, C. A. S.), incomplete. Anterior caudal (No. 4557, C. A. S.), incomplete. Anterior caudal (No. 4558, C. A. S.), incomplete. Anterior caudal (No. 4556, C. A. S.), incomplete. Median caudal (No. 4554, C. A. S.), incomplete. Median caudal (No. 4552, C. A. S.), incomplete. Posterior caudal (No. 4550, C. A S.), incomplete. Posterior caudal (No. 4551, C. A. S.), incomplete. Posterior caudal (No. 4553, C. A. S.), incomplete. Sternal segments (Nos. 4431, 4433, 4434, C A. S.). Right mandible (No. 4487, C. A. S.), posterior end missing. L^ft mandible (No. 4488, C. A. S.), posterior end missing. Right mandible (No. 4489, C. A. S.), anterior extremitj' only. Left mandible (No. 4490, C. A. S.), anterior extremity only. Extremity of left premaxilla with canine (No. 4427, C. A. S.). Aside from it.s much larger size and the tooth modifications, the general aspect of the skull of AJlodesmus kernensis may have resembled somewhat those of the White River Oligocene cats, Hoplophoneus priincevus and Dinictis felinus. with a shortened face, short and heavy rostrum, massive mandibles, backward prolongation of superior portion of the supraoc- cipital, and expanded zygomatic arches. The backward pro- longation of the median apical portion of the supraoccipital considerably beyond the level of the condyles, and the presence of a strong vertical median ridge, which acts as a brace for the lambdoid crest, are qyite unlike the retreating curvature of the vertex of the supraoccipital in living otariids. Both Dinictis and Hoplophoneus have mandibles with a pronounced genial tuberosity, but this tuberosity is much reduced in AUo- desnius. It is possible that Allodesnuis may have been derived from a progenitor whose mandible had a somewhat larger genial tuberosity, but it is equally probable that the dexelop- ment of a genial tuberosity in Dinictis and Hoplophoneus accompanied the elongation of the canines, and that it bears some relation to the functional use of these teeth. Further- more, in case of Dinictis and Hoplophoneus, not more than 23? CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. two or three of the upper and lower premolars are present, but one upper molar remains, and the lower molars are reduced to one or two. In both of these felids, the fourth upper premolar is the carnassial, while in AllodestJius the upper cheek teeth appear to proii^ressively diminish in size from the anterior to the posterior end of the series. In the mandible, the fourth premolar is the largest cheek tooth. The carnassial teeth are not differentiated in either the upper or the lower premolar- molar series. Furthermore the large canines are equally devel- oped in the upper and lower jaws of AUodesmns. As with Allodesmus, these Oligocene cats have a consolidated scapho- lunar-centrale. Patriofclis* from the middle Eocene of the Bridger Basin, Wyoming, has an outwardly curved premolar-molar series, so it would appear that Allodesmus retains some of the creodont heritage, especially in the curvature of the upper cheek teeth, the persistence of two small upper molars, and the location of the antorbital foramen at the level of Pm*. But Patriofelis with its large, massive skull, shortened face, broadly and abruptly truncated rostrum, and shearing M^ and M, does not seem to possess any close phylogenetic relationship with Allo- desmus. The enlarged and powerful second lower molar, according to the general rules of probability, would not be expected to disappear in dental reduction. Furthermore, the scaphoid, lunar, and centrale are separate bones in the carpus of Patriofelis. The pelvis also presents a number of anatomi- cal characters not found in Allodesmus. Some of the MiacidcT^ have an outward bowed upper molar- premolar series, especially Miacis and J'assacyon. Matthew** has shown that the scaphoid, lunar, and centrale are consoli- dated in Vulpavus profectus, and it is possible that the fusion of these elements may have taken place in other members of this family of creodonts. There is no available evidence to show that the consolidation of the scaphoid, lunar, and centrale has taken place since entering an aquatic environment, and, in < T. L. Wortman. Bull. Amer. Mus. Nat. Hist., vol. 6, art. 5. 1894, pp. 129-164, pi. 1, figs. 1-5. — W. D. Matthew, Mem. Amer. Mus. Nat. Hist., vol. 9, pt. 6, 1909, pp. 420-432, figs 50-52. " W. D. Matthew & W. Granger. A revision of the Lower Eocene Wasatch and Wind River Faunas. Bull. Amer. Mus. Nat. Hist., vol. 34, art. 1, 1915, pp. 33-34, 41-42. • W. D. Matthew, Mem. Amer. Mus. Nat. Hist., vol. 9, pt. 6, 1909, p. 388, fig. 29. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 233 the absence of such confirmatory evidence, it would seem that the otariids were descended from terrestrial creodonts in which these carpal elements were consolidated. Inasmuch as the carefully considered evidence assembled by Matthew^ and Gidley* seemed to indicate that the clsenodonts were progressing toward the Ursidae in the distinctive charac- ters of the teeth and feet, it was necessary to examine their possible relationships to the Otariidae. In a more recent com- munication." however. Doctor Matthew questions the sup- posed relationship between the Arctocyonidse and the Ursidae. In the carpus of Cla^nodon and Neoclcenodon the scaphoid and centrale are fused, and, although the lunar-centrale facet per- sists, the lunar-scaphoid facet has disappeared and is replaced by a roughened bony surface. These details seem to point to the imminent union of the scaphoid and lunar. The tarsal bones exhibit a number of distinctive features not found in any of the Otariidae. The astragalus of Allodesmus kernensis differs from that of Neoclcrnodon montanus (No. 9779, U. S. N. M.) in having (1) the trochlea continued farther proximally in a plantar direction; (2) the astragalar foramen open or closed; (3) a narrow oblique groove for the flexor digitorum on the tibial border of plantar prolongation of the body, in contrast to the unusually broad groove which occupies most of the plantar prolongation of the body in Neoclcenodoii ; and (4) the head less flattened and narrower from side to side. Although the calcaneum of Allodesnius is quite similar in general shape to that of NcoclcEiwdon (No. 8362, U. S. N. M.) it differs in having (1) a shorter stouter shaft, (2) a less proximally extended sustentacular facet, (3) a narrower distal facet for the cuboid, (4) a shallower interosse- ous groove between ectal and sustentacular facets, and (5) a less protuberant peroneal tubercle. The cuboid of Allodesmus differs from that of Neoclcenodon (No. 8362, U. S. N. M.) in having (1) a relatively smaller ' W. D. Matthew, Additional observations on the Creodonta. Bull. Amer. Mus. Nat. Hist., vol. 14, art 1, 1901. pp. 14-15. ' J. W. Gidley, New species of Claenodonts from the Fort Union (Basal Eocene) of Montana. Bull. Amer. Mus. Nat. Hist., vol. 41, art. 14. 1919, pp. 541-55, text fig. 10, pi. 28. * W. D. Matthew, The evolution of the mammals in the Eocene. Proc. Zool. See. London, 1928, p. 971. January 30, 1931 234 CALIFORNIA ACADEMY OF SCIENCES [Phoc. 4th Seb. and more convex facet for calcaneum; (2) a more oblique curvature of astragalar facet and a more reduced navicular facet: (3) a reduced proximal facet for ectocuneiform ; and (4) the presence of facets on distal en(i for metatarsals IV and V, whereas there is but a sinijle facet on the cuboid of Xeoclcunodon. ]\Iatthew has called attention to ( 1 ) the slender, serrate, and unworn canines: (2) the reduction of the premolars; and (3) the presence of low-cusped quadrate molars, with lower M^ somewhat reduced. The derivation of the Otariidre from the clrenodonts is beset with several obstacles, inasmuch as the clrenodonts are characterized by, (1) the presence of a protu- berant, outwardly curved, lesser trochanter below the head of the femur: (2) the presence of a distinct third trochanter at a lower level on the external border of the shaft: (3) the pres- ence of an entepicondylar foramen in the humerus: (4) the fact that the upper M" and the lower Mg are the largest of the cheek teeth and hence would not be expected to be reduced in the course of dental reduction: and (5) the presence of keeled, fissured, ungual phalanges, with no trace of a basal sheath. In view of the debatable nature of the evidence which has been brought forth to support the theory of the derivation of the otariids from members of several families of creodonts, it would appear that they can not be derived from any known genus, and, in so far as some osteological characters are con- cerned, the Otariidce may retain as much of the felid heritage as they do of the ursid heritage. The dentition of the Otariid?e is quite unlike either of the last mentioned groups. The foregoing remarks are intended to supplement the sum- mary^" published in 1922. Xexertheless it would appear that in the progressive evolution of the otariids, (1) the facial region was deepened: (2) the spreading or outbowing of the zygomatic arches was reduced: (3) the antorbital foramen was moved backward: (4) one lower incisor was lost: (5) the first upper premolar was lost: (6) the upper and lower molars were reduced in size; (7) the premolar-molar .series were moved inward with the side to side compression of the rostrum and the opposite row^s became nearly parallel: (8) the notch '» R. Kellogg. Univ. Calif. Piibl., Bull. Dept. C.eol. Sci., vol. U. no. 4. 192J. pp. 94-9;. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 235 between the palatal portion of the maxillary and the jugal was widened; and (9) the posterior narial gutter was closed in by the narrowing and backward prolongation of the palatal region. Rostral fragments of the skull of Allodestnus kernensis, X 0.5. Fig 4. Palatal view of right and left rostral fragments, Nos. 4397 and 4396, C. A. S. Fig. 5. Lateral view of left rostral fragment, No. 4396, C. A. S. 236 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Skull Portions of the rostrum of at least two and possibly three individuals are represented in this collection. Of these, a por- tion of the left maxillary (No. 4396, C. A. S.). with large canine, roots of Pm- and Pm^, as well as the alveoli for Pm*, M^ and M", is the most nearly complete. A portion of the right maxillary (No. 4397. C. A. S.) with alveolus for canine, the root of Pm*, and the alveolus of Pm'^ seems to belong with specimen No. 4396, C. A. S., but there is no certainty that this association is correct, since the two portions of the rostrum were in separate packages when received. There is in addition to the above, a fragment of another right maxillary (No. 4426, C. A. S.) bearing a large canine tooth and alveoli for a small Pm\ a rather large Pm", and smaller Pm^ and Pm*. The occipital region of the skull" of this fossil pinniped was described in 1922. By referring to text fig. 4. it will be seen that the rostrum of this pinniped differs from all living otariids in having an outwardly curved premolar-molar series, with Pm*, M\ and M" actually outside of the level of the antorbital foramen, whereas in the living Eumetopias. Zalophus, and Arctoce- phahis, the two series are nearly parallel and lie within the level of the antorbital foramina. That portion of the maxil- lary which forms the roof for the antorbital foramen is miss- ing, but the anterior orifice of the latter lies at the level of Pm*. Although the peculiar outward curvature of the pre- molar-molar series is quite unlike any living pinniped, it is obvious that the cheek teeth were not carried backward upon the anterior end of the zygomatic arch, for the small second upper molar is placed within, and anterior to, the narrow notch between the antero-inferior process of the jugal and the palatal portions of the maxillary. The number of upper incisors is unknown. The canine is a large recurved tooth, with crown covered with a thin coat of enamel. The alveolus of a small Pm' is present on one specimen (No. 4427, C. A. S.), but no trace of it can be found on the larger rostral fragment (No. 4396, C. A. S.). It is barely possible that this tooth may belong with the milk dentition, since it lies slightly internal to » R. Kellogg, Univ. Calif. Publ., Bull. Dept. Geol. Sci.. vol. 13, no. 4, 1922, pp. 29-32, text figs. 2a-2b. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 237 the much larger succeeding premolar. Assuming that this represents the alveolus of the first upper premolar, then the second upper premolar has the largest root of the premolar series and may have had a larger crown than the others. The alveoli of the cheek teeth progressively decrease in size from the anterior to the posterior end of the series. The roots of all the cheek teeth were implanted obliquely, and, with the exception of the molars, all were implanted on the outer edge of the maxillary. The almost horizontal direction of the ah^eolus for the small second upper molar seems to offer an explanation for the loss of this tooth by the living genus Eumetopias. The direction of this alveolus indicates that the tooth could hardly function in any normal manner, and hence would tend to be reduced in the course of time. The upper cheek teeth appear to consist of four premolars of which Pm^ is usually missing, and at least two small molars. It is impos- sible to determine from the material at hand whether or not this form has a third upper molar. Viewed from the side (fig. 5), the depth of the maxillary (54 mm., No. 4396, C. A. S.) at the level of the antorbital foramen is about one-half of that (98 mm.. No. 7140, U. S. N. M.) of an old adult Eumetopias juhata. The sinuous curvature of the superior margin of the maxillary of Eume- topias also is quite unlike the sloping margin of the maxillary of this fossil pinniped. The premaxillary and the incisors are missing. The external narial orifice is narrower and the infra- orbital portion of the maxillary is prolonged farther backward than in any living otariid. The skull of Allodesmus differs from that of Eumetopias in having ( 1 ) the premolar-molar series curving outward and ending near level of anterior end of zygomatic arch; (2) at least five functional upper cheek teeth which decrease in size from anterior to posterior end of the series; (3) a rather large second upper premolar; (4) no indication of a basi- rostral constriction; (5) an obvious backward prolongation of infraorbital portion of maxillary; (6) antero-inferior process of jugal extending forward to level of first upper molar; (7) a wider palate; and (8) a conspicuous lambdoid crest, with median apical portion prolonged backward. 238 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Amoni,' the fragmentary and more or less complete teeth referred to Allodesmus kernensis are two molars, nine pre- molars, and three canines. The molars have small crowns and unusually short roots. All of the premolars have rather long roots, and many of them have a pronounced longitudinal external groove. The crowns of all these cheek teeth have the appearance of being covered with fairly smooth enamel, although on closer inspection it will be seen that it is finely pitted. With the exception of the larger premolars, all of the cheek teeth have rather low crowns, with the apical portion curving inward. The base of the crown is swollen and its cir- cumference is greater than that of the root. Two of the larger premolars exhibit rudiments of basal nodosities at the postero- internal angle. The roots of the cheek teeth are often asym- metrical and taper irregularly, but the pulp cavity is closed. The large canines, with recurved crowns which often pass im- perceptibly into the neck, have an open pulp cavity. Three teeth, with strongly recurved apices and pronounced basal rugosities on the internal face, agree sufficientlv with the incisors of Eumetopias to be considered such. The crown is but slightly swollen at the base, and the root has a distinct neck, below which is a pronounced enlargement. The pulp cavity in the roots of these teeth is closed and the roots are asymmetrical. Mandible Portions of seven mandibles belonging to individuals of dif- ferent sizes agree with the type mandible of Allodesmus ker- nensis^"^ in all their essential details. Three of these belong to large individuals and they are, respectively, a nearly complete left mandible (No. 4395, C. A. S.) : an incomplete right man- dible (No. 4426, C. A. S.) ; and a section of a left mandibular ramus (No. 4486, C. A. S.), having both ends missing. Four belong to considerably smaller individuals, possibly females or voung males, and are apparentlv the anterior halves of the right (No. 4487, C. A. S.) and the left (No. 4488. C. A. S.) mandibles of one individual; the anterior extremity of a right ^ R. Kellogg, Univ. Calif. Publ. Bull. Dept. Geol. Sci., vol. 13, no. 4. 1922, pp. 26-28, figs, la, lb. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KEKX RU'ER REGIOS 239 Incomplete left mandible of AUodcsmiis kernensis, No. 4395, C A. S., X 0.5. Fig. 6. "Internal view. Fig. 7. Dorsal view. Fig. 8. External view. mandible (No. 4489, C. A. S), and the corresponding portion of another right mandible (No. 4490, C. A. S.). The largest of these mandibles lacks the coronoid process, the condyle, and the angular process. This left mandible (tig. 8) is approximately the same size as the type right mandible and is much more nearly complete. The canine and the tirst premolar are in place, and there are, in addition, alveoli for two incisors, three premolars, and two molars. As compared 240 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. with the corresponding mandible of a large adult Euiuetopias jnhata (No. 7140, U. S. N. M.) this fossil mandible is charac- terized by a longer and more oblique symphysis, a somewhat deeper ramus, a more posterior and shallower masseteric fossa, and a more pronounced genial tuberosity. The number and position of the mental foramina agree with Eumetopias, but the cheek teeth are larger, and the outer incisor is considerably larger. The external face of the mandibular ramus (fig. 9) is flat- tened superiorly, but, taken as a whole, the external surface exhibits a convex curvature and the internal a concave curva- ture. The ramus is about as thin as in Eumetopias. The sym- physial surface (fig. 6) is deeply pitted and corrugated as in Eumetopias, indicating that the opposing mandibles were appressed very closely and bound together by ligaments. The alveoli of the cheek teeth (fig. 7) are very closely spaced, the length of the lower series measuring 141 mm. from the anterior margin of the canine to the posterior border of the alveolus of the second lower molar in the largest mandible (No. 4395, C. A. S.). The antero-posterior diameter of the crown of the first lower premolar is 11.7 mm. (No. 4395, C. A. S.). The corresponding measurement of the third lower premolar is 13.6 mm. and that of the first lower molar, 11.5 mm., in another left mandible (No. 4486, C. A. S.) of approximately the same size. The curvature of the superior border of the last mentioned mandible indicates that the coronoid process slopes more gradually upward than in Eumetopias. The rounded crowns of the first lower premolar, the third lower premolar, and the first lower molar are covered with fairly smooth enamel. The enamel crowns of less worn cheek teeth are often finely pitted. The available evidence indicates that AUodesmus is not ancestral to Dusignathus^'^ and that the living Eumetopias may be a derivative of AUodesmus. Dusignafhus differs from AUodesmus in having ( 1 ) a shorter and lighter mandibular ramus; (2) cheek teeth with larger roots, without pronounced longitudinal external groove; (3) crowns of cheek teeth with smooth, highly polished enamel in contrast to finely pitted enamel of AUodesmus cheek teeth; (4) loss of second lower " R. Kellogg, Fossil Pinnipeds from California. Publ. 346, Carnegie Inst., Wash- ington, 1927, pp. 27-33, text figs. 1-6. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERX RIVER REGIO!^ 241 molar; (5) more oblique slope of anterior margin of coro- noid ; and (6) strong convexity of lower mandibular border between genial tuberosity and lower angular process. Measurements of Left Mandible (No. 4395, C. A. S.) Greatest length of symphysis 106.0 mm. Depth of ramus between fourth premolar and first molar.. 62.0 mm. Antero-posterior diameter of alveolus, first incisor 12.0 mm. Antero-posterior diameter of alveolus, second incisor 8.5 mm. Antero-posterior diameter of alveolus, canine 32.0 mm. Antero-posterior diameter of alveolus, first premolar 13.2 mm. Antero-posterior diameter of alveolus, second premolar... 16.4 mm. Antero-posterior diameter of alveolus, third premolar 17.0 mm. Antero-posterior diameter of alveolus, fourth premolar.... 17.8 mm. Antero-posterior diameter of alveolus, first molar 12.2 mm. Antero-posterior diameter of alveolus, second molar 8.0 mm. As compared with the mandible of an old adult Eiimetopias jiihata (No. 7140, U. S. N. M.) this fossil mandible (No. 4395, C. A. S.) has: (1) a canine with a narrower root; (2) larger and more crowded cheek teeth; (3) considerably longer premolar-molar series; (4) a small second lower molar; (5) a distinct interval between the fourth premolar and the first molar; (6) cheek teeth with no in'dication of a cingulum or fringe of basal rugosities; (7) a more posteriorly situated inner incisor; and (8) a much larger outer incisor. The mandibles of the smaller individuals agree in all essen- tial details with the larger mandibular rami, but are lighter and have smaller teeth. The left mandible (No. 4487, C. A. S.) of one of these has a canine with a complete crown, which is recurved and somewhat compressed from side to side, but without any indication of anterior or posterior carinae. The symphysis of this mandible is less pitted and less rugose than in those belonging to larger individuals. Vertebra The vertebral column of an old male sea lion (Euinetopias jubata) is considerably larger than that of young males and old females, and it would appear from the present material that sexual dimorphism was equally well marked in Allo- desmus. Seven cervical vertebrae belonging to a very large 242 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Atlas of AUodesmus kerncnsis. No. 4398, C A. S., X 0.5. Fig. 9. Ven- tral view. Fig. 10. Dorsal view. individual are referred to an old male. Unfortuntely most of these vertebrae are badly damaged. One nearly complete atlas (No. 4398, C. A. S.) and another damaged one (No. 4414, C. A. S.) show that this vertebra in Allodesuius differs very little from the corresponding bone in Eumctopias jubata. The antero-posterior diameter of the neural arch (fig. 10) is rela- tively greater, and the transverse processes are less incurved. The neural arch is perforated on each side by a large vertebrar- terial foramen, and postero-internally on each side is the orifice of the canal that passes through the transverse process and Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 243 emerges on its internal face at a point more than half way to the extremity. The articular surface for the odontoid, as well as those for the facets on the anterior face of the centrum of axis, corresponds with that of Eumetopias. Not even a vestige of the neural spine is retained. The anterior articular surfaces (fig. 11) for the condyles of the skull are deep and strongly concave. The curvature of these facets is likewise similar to that in Eumetopias. As seen from the ventral side (fig. 9), this fossil atlas differs from that of Eumetopias in having transverse processes with larger fossae through which the vertebrarterial canals pass. The fifth cervical (No. 4407, C. A. S.) is incomplete, with both epiphyses, neural spine, and transverse processes missing. The neural arch is lower and less vaulted, but the size, shape, and direction of the pre- and post-zygapophyses agree with those in the corresponding cervical of Eumetopias. Further- Atlas of Altodesmus kernensis, No. 4398, C. A. S., X 0.5. Fig. 11. An- terior view. Fig. 12. Lateral view. 244 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. more, the lateral vertebrarterial canal is slightly larger, the neural arch is much wider, and the transverse process is about three- fourths as broad at the base. ? Sixth cervical vertebra of Allodesmus kernensis, restored, No. 4399, C A. S., X 0.5. Fig. 13. Anterior view. Fig. 14. Lateral view. Two vertebrae, which have the same structural characters as the sixth cervical of Eumetopias, are included in this collec- tion. The larger of the two lacks most of its processes, but the other one is fairly complete. The latter lacks, however, both epiphyses and both diapophyses ; the right postzygapo- physis is missing and the left transverse process is incomplete. In general shape this fossil cervical exhibits a surprising resem- blance to the sixth cervical of Eumetopias, but the forward inclination of the neural spine is less pronounced, the prezyga- pophyses are wider apart, and the postzygapophyses have more oblique articular facets. Viewed from the front (fig. 13) the neural canal is broader, the lateral vertebrarterial canals are larger, and the centrum is broader. The lateral aspect (fig. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 245 52 s s "r; is, « o M 5 O 1/1 rt r^ OC 00 CN OC ON r<^ I •* NO ir- r^ f-» .-^ t-- NC d NO H u. o 0 0 0 O 00 C OC c Ov OC c On 00 v-H aa-^ g.a nee een ide ins ga- yses o o XT' \r «N CNi r<- c OO >0 .^ P ^ l_i O N ^ o- o ir- ^- vC CN C c O fO « t^ a "! " S* 00 1- O t^ o> O OC c —■ 00 5^5E ^a ■'^ »-H -i.S^g^ IT" c IT" r<- C OC lO 't t- f^. c lo o ■2 t C oj 5-? «J (U (U J=- fl^ o (u ^ is E ^ t, J C w rt ■= rt r*; ir rr 't r— c t^ ^M \n CN CN ^ d rr. CN ■<* r<- r<; rr: ^- -+ PO fr ■>* « " ft-d o ngth trum lO I'' CM c r<- tN tN u- rs c «o OO ir I/- 00 fN r<" f' Tf NC OC o- 1^ c t^ ": NO CN c «— 1 a C r<^ f C t-- r-- XT •i 1^ vC Tt 00 NO u- OC t^ Least intero- osterior iameter of uperior surface f neural arch II a-d w -- o Distance across vertebra between outside margins of anterior articular facets CM ir- Ov C C OC o C m5 g o o « OO c c^ CN CN rt o 0) g „ a^ ,-« ■* 0^ r^ vO CN ^ ^H s ^H 2«i«_g^-0ft *-H *-N '-" T-( nee >ss bra een of •erse sses ^-f lO •* O t~-. ^ 00 Tt< o Z Z <-) Z Z to Z -o -G -o -o J,^ -a 5^ 2: .s a Scapula An incomplete left scapula (No. 11857, U. S. N. M.) is referred to this fossil otariid. The superior border, the pos- terior half of the blade, and the spine are missing. None of the living Otariid?e possess a scapula of this type. One of the most unusual peculiarities of the bone is the outward curva- ture of the prescapular portion of the blade. A prominent broad ridge extending upward from the neck toward the verte- bral border separates the deep prescapular fossa from an obvi- ously similar postscapular fossa. The neck of this scapula (fig. 19) is unusually long. The glenoid cavity is large, strongly concave, with its posterior diameter more than twice the width of the anterior diameter. Neither the acromion nor the coracoid process are present. Measurements of the Scapula Antero-posterior diameter of glenoid cavity 61.0 mm. Greatest transverse diameter of glenoid cavity 49.-l-mm. Posterior margin of broad subvertical ridge to antero- inferior angle of blade (measured at the same level) 110.0 mm. January 30, 1931 250 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Ser. Fig. 19. Incomplete left scapula of Allodesmus kerncnsis, No. 11857, U. S. N. M., X 0.5. Humerus Distal and proximal fra<^ments of a rii^ht humerus (Nos. 4337, 4338, C. A. S.), which may he portions of one bone, and the distal epiphyses of a very large left humerus (No. 11858. U. S. N. M.) are all that are known at present. The dis- tinguishing characteristics of this fossil humerus may be summed up as follows : ( 1 ) the inner condyle is placed very low, judging from its proximity to the distal margin of the inner trochlea; (2) the anterior border of the deltoid crest does not overhang the shaft to any appreciable extent on the outer side; (3) the longitudinal ridge below the lesser tuberosity is feebly developed; (4) the transverse diameter of the posterior face at the proximal end of the shaft exceeds by one-sixth the antero-posterior diameter of the shaft below the deltoid crest; and (5) the upper portion of the shaft is rather slender in comparison to that of Eumetopias. The proportions of these fragments suggest a humerus of approximately the same size as that of a female or young male Eitinetopias juhata. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 251 Viewed from the front the shaft tapers gradually toward the distal extremity, and the proximal end is unusually narrow as compared to its length. The entire proximal epiphysis, in- cluding the head and the greater and lesser tuberosities, is missing. The deltoid ridge (fig. 20) is rather high, and, although its anterior border is somewhat eroded, there is nothing to indicate that the external margin was produced outward as in Enmetopias. At the distal end, the deltoid crest rises rather abruptly, and the anterior margin for most of its length is straight as viewed from the side. The posterior face of the proximal one-third curves strongly backward. The trochlear surface (fig. 21) for articulation with the bones of the forearm is divided as usual into two main areas. The outer convex capitulum which articulates on the head of the radius, and the inner trochlea which rests in the greater Fragments of humeri of Allodesmus kerncnsis, X 0.5. Fig. 20. External view proximal end of shaft of a right humerus, No. 4337, C. A. S. Fig. 21. Distal view of a right humerus, No. 4338, C A. S. Fig. 22. Distal view of a left humerus, No. 11858, U. S. N. M. 252 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. sigmoid cavity of the ulna, do not differ in any essential fea- ture, when viewed from the front, from the corresponding sur- faces of the humerus of Eiimetopias. On the posterior face, however, the trochlea is considerably narrower. The width of the trochlear surface on the large left humerus (fig. 22) exceeds 98 mm., and thus exceeds the width of a very large old male Eumetopis jiihata. Measurements of Humeri (in millimeters) No. 11858, U.S.N.M. Left, Allodesmus kernensis No. 4338, C. A. S. Right, Allodesmus kernensis No. 4337, C. A. S. Right, Allodesmus kernensis No. 21537, U.S.N.M. Left. Eumelopias jubala Width of trochlear surface on the an- terior face 97.+ 73.0 51.0 55,5 68.5 73 5 Width of trochlear surface on the pos- terior face 70 8 Transverse diameter of shaft below head 91.0 Antero-posterior diameter of shaft near the micldle (through deltoid crest) . . . 74.5 Radius In spite of their weathered and eroded condition, certain peculiarities, in addition to size which may or may not be of importance, appear to differentiate into two categories the radii represented in the material submitted for study. The writer, nevertheless, is not disposed to stress the importance of characters observed on the proximal ends of the two radii belonging to large individuals (Nos. 4293, 4406, C. A. S.) and the corresponding portions of radii of three smaller indi- viduals (Nos. 4291, 4292, C. A. S., and No. 11863, U. S. N. M.). The heads of all these radii are more or less eroded and consequently the original contour of the proximal surface can not be determined with any degree of certainty. At the level of the bicipital tuberosity, the necks of the radii would appear subtriangular in cross section. The upper ulnar facet of one of the smaller radii (No. 4292, C. A. S.) measures 17 mm. in depth and the same measurement for one of the larger radii (No. 4406, C. A. S.) is 26.6 mm. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 253 Radii of Allodesmtis kerncnsis, X 0.5. Fig. 23. Posterior view of right radius, No. 4406, C. A. S. Fig. 24. Internal view of right radius, No. 4292, C. A. S. Fig. 25. Distal view of right radius, No. 4292, C. A. S. Fig. 26. External view of right radius, No. 11866, U. S. N. M. Fig. 27. Distal view of right radius. No. 11866, U. S. N. M. 254 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Skr. Compared with the radii of Eiimetopias juhata, these fossil radii are much longer and slenderer, less expanded at the level of insertion of pronator radii teres, and have a larger facet for distal end of ulna, a more squarely truncated anterior border of facet for scapho-lunar, and a more distal position for the bicipital tuberosity. The right radius (fig. 24) of a smaller individual is fairly complete, but the distal extremity is some- what eroded. The distal one-third of a right radius (fig. 25) is better preserved. In addition to these two there are por- tions of the proximal ends of three right radii of animals of approximately the same size. The following features seem to characterize the radius in smaller individuals: (1) the narrowness of the shaft at the level of the insertion of the pronator radii teres; (2) the long neck; (3) the presence of a broad depression on the posterior face of the shaft for the insertion of the interosseous liga- ment; and (4) the low position of the bicipital tuberosity. On the other hand, the radius in larger individuals has : (1) a much thicker neck; (2) the large facet for the capitu- lum of the humerus occupying practically the entire proximal surface of the head, and the trochlear facet limited to a narrow border on the internal side; and (3) a less distinct bicipital tuberosity. Measure inents of Radii (in millimeters) wi in S .2 i. .2 tn i •rt"- ^ oo' ■r}< •.-( VO .-Hio '^ CO '-I (N .^ ^ c c < \ ( ! ! < ■♦ ■4 c y s ■^ X " SI 3 a i - ^ c 2 o c - "^ -^ 2 '^ * " S2 z > (. S +-> ( /I uj J; hi ii ' 1 . u . ri . G • -(-> ■> +j J ^+-1 : a :! ^ D O D O ^ § Ml : '=5 : .22 c ■ -« 1 • D c ■ si : '-S 5 ■ ^ c J I/) •- ■> QJ o »-> 3 J 2 c n - c 2 { c ; '3 . c o • +J : S • fe ' i 3 .2 3 '^ H t« > *-* J 0) u > - 4- ^ J ■(-> ^ 3 O ■ e ■ w :.S :"^ : S3 • +j • • G : 2 t a; i O ; »ii . rt . c • +j ; rt . w :- ■ s • '>. : T} . c . o . o I-I • 4^ • c c ;^ t • -4- . S- . c . j: 0 . c : -c . : . a ! c i t ■J J +■ £ '^ P - c '' C 5 f i C ^ £ 3 4- j c H 4- Z <4 ■^ c :! -^ -> + 3 "^ a c J J 3 a 3 3 < :> -> ■H d -< 0 H .J 3 a 3 o 272 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. mm. in length, respectively. Before taking up in detail a con- sideration of these smaller femora, it seems advisable to dis- cuss their relationship to another femur^" described from the same deposits in a previous paper. It is now apparent that the left femur associated with the type mandible of Allodcsrnns kernensis belongs to a young individual and that in all proba- bility it does not belong to the same individual as the jaw. This femur, unlike the two hereinafter described, has a fairly distinct intertrochanteric crest. These smaller femora present all the salient features of the larger femora described above. Anteriorly the shaft is more or less flattened at the distal end and proximally the surface slopes to the outer border, giving the shaft a twisted appearance. Turning to the posterior face we find that there is no indication of an intertrochanteric crest and that the lesser trochanter is represented by a low elevation. The trochanteric fossa is well defined, but the internal crest, or tubercle, which is developed on the larger femora, is miss- ing. The depression at the distal end of the anterior cruciate ligament is well defined. In comparison with those of the larger femora, the neck, which supports the head, appears to be proportionately thicker than the portion of the shaft which bears the greater trochanter. Patella The knee joint of this fossil pinniped was protected by a large patella. The base of this sesamoid bone is more or less quadrangular in outline and is furnished with a large, oval, concave, articular surface whose main axis is oblique to the proximo-distal axis of the patella itself. The distal angle of this bone is drawn out into a rounded peak, and the major portion of the anterior surface slopes to the proximal margin. Beginning near the middle of the external border and curving around the distal face is a broad groove for some ligament. A similar groove, with less sharply defined margins, is present on the internal border. Nine patellae ranging in size from one with a proximo-distal diameter of 62.5 mm. to one measuring not more than 45 mm. were sorted out of this collection. At the distal end, the largest of these sesamoids has a depth of " R. Kellogg, Univ. Calif. Publ. Geol. Sci., vol. 13, No. 4, 1922, pp. 39-40, text figs. 14a-14b. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN' RIVER REGIOS 273 45 Fig. 45. Patella of Allodcsmus kernensis, No. 11544, U. S. N. M., X 0.5. 41.2 mm. and the corresponding measurement for the smallest is 30.4 mm. Most of these sesamoids are more eroded than the one here figured (fig. 45). Tibia Comparison with the tibiae of living otariids indicates that the tibia (No. 4304, C. A. S.) of young males or females of Allodesnius kernensis may be distinguished by the following combination of characters: (1) shaft irregularly three-sided, but without distinct anterior longitudinal crest; (2) proximal end of shaft not fused with head of fibula; (3) posterior sur- face of shaft distinctly flattened; (4) posterior intercondyloid fossa relatively small and anterior intercondyloid fossa almost obliterated; (5) intercondyloid eminence relatively low; and (6) a single groove for tendons of tibialis posticus and flexor muscles of the foot on internal border of posterior surface of distal end of shaft. The left tibia (fig. 46) of this fossil pinniped has about the same proportions as the corresponding bone of the living sea lion (Eumctopias jnhata), but differs from the latter in that it was not united with its neighbor, the fibula, at the proximal end. This fossil tibia is, nevertheless, slightly shorter than that of an adult Eumetopios jnhata (Xo. 21537, U. S. N. M.). 274 CALIFORNIA ACADEMY OF SCIENCES [Pboc. 4th Ser. Left tibia of Alodcswus kcrnensis, No. 4304, C. A. S., X 0.5. Fig. 46. External view. Fig. 47. Proximal view. Fig. 48. Distal view. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 275 Inasmuch as the condyles of the femur articulate with the proximal expanded extremity of the tibia, condylar facets of corresponding proportions are developed on this surface (fig. 47), the external articular facet being somewhat larger than the internal. Both condylar facets are more or less flattened in comparison to those on the tibia of Enmetopias juhata and the intercondyloid eminence is not as prominent. The posterior intercondyloid fossa is much shallower and slightly narrower than in Enmetopias. Whereas, the anterior intercondyloid fossa is rather broad and deep on the tibia of the recent sea lion, it is almost obliterated on this fossil bone and is limited to a small pit whose area is even less than the rounded inter- condyloid eminence. The external condyle overhangs the shaft to a greater extent than the internal, a modification correlated with the position of the fibula. The roughened surface for the head of the fibula is placed postero-externally on the distal sur- face of the overhang produced by the lateral expansion of the condylar facet. A shallow facet for the patella is present on the anterior face of the proximal end of the tibia, and this sur- face terminates on each side at the internal margin of the con- dylar facet. The shaft of the tibia is irregularly three-sided, possessing an anterior, an external, and a posterior surface. The expanded extremities of the shaft support the epiphyses which bear the articular facets. The longitudinal anterior crest, which defines the limits of the anterior and external surface, is not as dis- tinct as in Enmetopias jubata, but the interosseous crest, which separates the external from the posterior surface, is as sharp- edged as in the living animal. The shaft itself is bowed for- ward and inward, and- is narrowest near the middle. The posterior surface of the shaft is distinctly flattened in com- parison to that of Eumetopias, there being only a slight indica- tion of the longitudinal depression for the tibialis posticus on the proximal third, but there is no trace of an oblique crest such as extends across the distal half of the tibia of the sea lion. The interosseous crest terminates about 28 mm. above the distal epiphysis, and below this the shaft expands to pro- vide an area for articulation with the distal end of the fibula. This fibular articulation facet is limited to the epiphysis of the tibia, and measures 26 mm. in width and 10 mm. in depth. 276 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Si;r. The posterior face of the distal extremity of the tibia of Eumetopias jubata displays two deep grooves, of which the mesial or tibial groove is the narrowest. The groove on the internal border is quite broad and is bordered by high crests. Over these grooves pass the tendons of the tibialis posticus and the flexor muscles of the foot. On this fossil tibia there is a single broad groove, bordered by low crests, which is placed on the internal border of the posterior face of the distal epiphysis. The distal end of the fossil tibia (fig. 48) is furnished with a saddle-like articular surface, which rests upon the trochlea of the astragalus. This articular surface is similar in contour to that on the tibia of Eumetopias, but the antero-posterior con- vexity is less pronounced. In front of and internal to this articular surface is the usual knob-like malleolus. There are, in addition to this specimen, the proximal end of a left tibia (No. 4492, C. A. S.), without the epiphysis, of a somewhat smaller individual, and the epiphysis of a right tibia (No. 4493, C. A. S.) from an individual about the same size as the one whose tibia is described above. Some idea of the size of a large individual of this fossil pin- niped is afforded by the proportions of this tibia (No. 4303, C. A. S.). By referring to the measurements given below, it will be seen that this tibia is considerably shorter than that of an old male sea lion (Eumetopias jubata) or of a walrus (Odobenus divergens). The shaft of the tibia of the walrus forms a sinuate curve, but that of the sea lion is bowed for- ward. This fossil tibia (fig. 49), however, has: (1) a shaft with a nearly straight anterior profile; (2) a very limited development of the proximal depression for the popliteus; (3) a single groove for tendons of the tibialis posticus and flexor muscles of the foot; (4) a narrow posterior intercondyloid fossa; and (5) a pit-like anterior intercondyloid fossa. The shafts of the right (No. 4302, C. A. S.) and left (No. 4303, C. A. S.) tibia are fractured transversely in two or more places, but are otherwise in a fair state of preservation. The epiphyses of these bones are not attached to the shafts. A proximal epiphysis for the tibia was included in the collection, but the remaining epiphyses were not found. The distal epi- Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 277 Left tibia and fibula of Allodesmus kernensis, Nos. 4303, 4305, C A. S., X 0.5. Fig. 49. Internal view. Fig. 50. Proximal view. 278 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Measurements of Tibiae (in millimeters) Greatest length of tibia .... Greatest diameter of shaft at distal end Greatest diameter of shaft at proximal end Transverse diameter of shaft at narrowest point Greatest diameter of proxi- mal epiphysis No. 4304, No. 4302, No. 4303, No. 7U0, C. A. S. C. A. S. C. A. S. U.S.N. M. Left, Right, Left, Left, Allodcsmus Allodcsmus Allodesmtis Eumelopias kernensis kernensis kernensis jubala 280.6 281.0' 296.5- 357.0 58.6 62.0 61.0 63.0 66.0 73.8 75.0 78.0 35.2 33.0 33.5 29.5 78.8 ' 91.0 98.5 No. 21331, U.S.N. M. Left, Odobenus divergens 374.0 71.0 98.0 37.8 103.7 ' Both epiphyses missing. - Distal epiphysis missing. physis (No. 4494. C. A. S.) of another large individual was secured. The proximal epiphysis of this fossil pinniped is very simi- lar to that of the smaller individual (No. 4304, C. A. S.). The articular surface of this proximal epiphysis (fig. 50) is furnished with a large external condylar facet and a consider- ably smaller internal one. The external condylar facet is slightly convex and the internal is shallowly concave, and the whole proximal surface is distinctly flattened, paralleling in this respect the head of the walrus tibia. The intercondyloid eminence is low, but the posterior intercondyloid fossa is reduced to a narrow re-entrant angle and the anterior inter- condyloid fossa is restricted to a small pit-like depression. In position and extent, the facet for the patella is similar to that of the smaller individual (No. 4304, C. A. S.). There is a pronounced overhang to the external condyle, notwithstanding the loss of a portion of the external border. On the proximal end of the shaft and below the overhanging external condyle is a roughened surface for the head of the fibula. When viewed from the side, attention is at once directed to the expansion of the extremities and to the mesial constriction of the shaft. The anterior profile of the shaft is nearly straight Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 279 and the external is strongly curved. While the shaft is roughly three-sided, the surfaces pass into one another so gradually that the anterior longitudinal crest is not developed and the external interosseous crest is visible only at the distal end. The tibia of the walrus is furnished with a well defined longitudi- nal depression on the proximal half of the posterior face of the shaft for the attachment of the popliteus. These fossil tibiae, however, are not similarly modified for this muscle. Two short crests below the posterior intercondyloid fossa indicate the position of this muscle. A single groove is present on the internal border of the posterior surface of the distal end of the shaft for the tendons of the tibialis posticus and the flexor muscles of the foot. Fibula Unfortunately, the head of the left fibula (fig. 49) is lost and the distal epiphysis is separated from the shaft. In the details of shape and of form the fibula of this fossil pinniped presents some variations from the usual otariid type. The shaft is slender and the extremities, especially the distal one, are enlarged. It has three lateral surfaces, the anterior, the posterior, and the internal or medial. The anterior surface of the shaft of the fibula increases in width from the proximal to the distal end. This surface is distinctly flattened and in this respect it is more like the fibula of Eumetopias than that of Odobeniis. There is no trace of an interosseous crest. This fossil fibula does agree with those of Eumetopias and Odohenus, however, in that the external border of the distal end of the shaft is fur- nished with a short crest, not more than 27 mm. in length. The posterior surface is convex and is continuous with the medial or internal surface except on the proximal fourth where they are separated by a sharp-edged, longitudinal crest. The proximal half of the shaft of the fibula of Odohenus is dis- tinctly flattened in a postero-internal direction, and in Eume- topias this flattening of the shaft is even more pronounced, but is limited to the proximal fifth. The corresponding portion of the shaft of this fossil fibula would appear triangular in cross section. 280 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Skr. The distal epiphysis is roughly pyramidal in form and is furnished with articular surfaces for the astragalus and the tibia. The articular surface for the lateral side of the astragalus resembles that of the walrus, and its general shape is quite unlike the corresponding facet on the fibula of the sea lion. This facet is constricted mesially, and may be described as consisting of a basal articular surface, which extends the full length of the tibial border, and a distal spatulate articular surface with crest-like margins. There is one feature, however, which is quite remarkable and that is the presence of a broad groove bordered by high crests on the posterior face of the distal epiphysis. There is an indistinct groove for a similar tendon on the fibula of Eiimetopias, but it seems to be undeveloped on the fibula of Odohenits. The facet for articulation with the tibia resembles that on the fibula of the walrus. Measurements of Fibulce (in millimeters) t No. 4305, C. A. S. Left, AUodesmus kernensis No. 21537, U. S. N. M. Left, Eumelofiias jubata No. 21331, U. S. N. M. Left. Odobenus divergcns Greatest length of fibula 280.5 30.0 43.8 15.8 252.4 37.4 30.7 6.7 367.0 Greatest diameter of shaft at proximal end Greatest diameter of shaft at distal end Least postero-internal diameter of shaft 41.0 54.2 14.0 Tarsus The tarsus of this fossil pinniped is quite similar in many respects to that of the living Eiimetopias jubata. There are. of course, important modifications in the individual tarsal bones. The calcaneum, for instance, is characterized by its thicker shaft and more expanded distal extremity, by the curvature and outlines of the sustentacular facet, and by the presence of a broad longitudinal groove on the internal face of Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 281 the greater process. The astragakis has a short neck and the postero-superior portion of the body is raised above the trochlea. It has in addition a distinct facet for the cuboid and a deep pit for the attachment of a tendon on the anterior bor- der of the articular surface for the navicular. The navicular does not have a facet for a sesamoid and the facet for the cuboid is rather narrow. The cuboid is characterized in part by the shallowness of the groove for the peroneal tendon. The entocuneiform, however, resembles that of Odobenits in having the proximal facet for the mesocuneiform extended across the fibular face. The other tarsal bones are unknown. Left calcaneum of Allodesmus kernensis, No. 4309, C. A. S., X 0.5. Fig. 51. Plantar or posterior view. Fig. 52. Dorsal or an- terior view. C\LCANEUM A very strong reason for considering that both sexes are represented among these eight calcaneal bones is the cor- responding disparity in size between the bones of male and female otariids. The five calcaneal bones (Nos. 4309, 4310. 4312. 4313. 4315, C. A. S.) referred to males of this species may be conveniently grouped according to size, the larger pair probably belonging to an old male and the smaller ones to young males. Size alone distinguishes the two larger cal- caneal bones (Nos. 4309, 4310, C. A. S.) from the three smaller ones. All of these tarsals are quite robust and the two January 30, 1931 282 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. larger ones are exceptionally well preserved. The three smaller calcaneal bones (Nos. 4312. 4313. and 4315, C. A. S.) are eroded and broken. The two larger calcaneal bones may have belonged to the same individual, inasmuch as they agree in size and appearance. The left calcaneum (No. 4309, C. A. S.) is the best preserved, and the following description is based largely upon this bone. Aside from its thicker shaft and more expanded distal extremity, the calcaneum (fig. 51) of this fossil pinniped bears a close resemblance to the corresponding tarsal of an old male Euinetopios juhata. As compared with the calcaneum of Odohenus divergens, this fossil tarsal is distinguished by the great side-to-side expansion of the distal extremity and by the twisting of the shaft toward the inside of the foot. The distal extremity of the calcaneum of Odobcnus is not disproportion- ate to the size of the head and the shaft is not noticeably con- stricted near the middle. The calcaneum of Eumetopias, how- ever, has the distal extremity expanded in the same direction as in this fossil tarsal. On the plantar face of this fossil cal- caneum and in the area corresponding to the heel, the distal extremity is provided with a smooth surface, and its proximal extremity is furnished with a broad groove for the accommo- dation of the tendon of Achilles. The anterior or dorsal surface of the calcaneum (fig. 52) is furnished with two large facets for articulation with the astragalus. Crossing the calcaneum near the middle is the greater facet on which the ectal facet of the astragalus articu- lates. This facet is constricted mesially and has raised mar- gins. Below this facet is the rugose sinuate groove for the interosseous ligament. To the inside of this groove is an elongated facet which extends across the internal half of the distal border of the calcaneum and is deeply concave in the direction of its long axis. Upon this articular surface rests the sustentacular facet of the astragalus. This facet differs in shape and direction from the corresponding facet on the cal- caneum of Eumetopias and Odohenus. In case of Emnetopias, this facet does not extend laterally to inner margin of the greater process but it does in case of Odohenus. No vestige of the broad longitudinal groove which traverses the internal face of the greater process of this fossil calcaneum was found Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 283 a o a V) a •S "V "O 'I- Iff' 'ON u^- ~r tN Lo o + LO tN lO Ol rr> iri rn rn o "5 "WN'S'n 'OtSll -ON COOOUllOl/^l/^lOOO vjvqnC soKfojiuin^ 000-*'-<'-iCN'.-lOO 'S 'V '3 'fiet 'ON ■;q3!>£ 'S 'V D '£lfi' 'ON SISU3UX311 snuisjpojlY 'S 'V 'O '01 et -ON o lO O 00 o O + LO to O ro O O O On '-' 00 O O t-— ■^ -^ -rf fO C-l 0\ sisu3UA3^ snuisipojiY 'S 'V "3 '6oet -ox O 00 -O O 1— LT. O ~", ■^ tN Ov O 00 'O I^ l^ vjvqnf svt(foi3mn^ •■p -pv 'WN'STl 'OflL 'ON lOlOOOl^OOOOOCN o 03 O ty ^ O o o "13 OJ U ^ "^^ •x} .^ ™ .S oJ ca O ft .2 P 6 xJ 'O OJ O +5 2 X o u 01 ■J) c« M tn cfl t/j CD a; 4-> +J +J -♦-> 4-> CTJ cd ca cd cd OJ Ih I. t-. U l-l o c o o o Ol S CS u-( CT3 73 ° ^ --g '-' . I (U Vh o ■M O c 6 « 111 ?* ■!-> +J rj u3 [« *J ■!-> -U 7) cij nl Cij 4) 4> OJ ^ u -) O CJ Og4 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. on the calcaneum of either Eumctopias or Odobenits. The peroneal tubercle on the other hand bears a close resemblance to that on the calcaneum of Eidmetopias. The external border of the distal extremity is traversed by a rather broad groove, over which probably passed the ligament for the extensor muscles of the digits. The distal surface of the calcaneum is furnished with a large facet for articulation with the cuboid. This facet is shallowly concave, with its transverse diameter approximately equal to its antero-posterior diameter. The anterior margin of the facet for the cuboid is co-extensive with the corresponding margin of the facet which articulates with the sustentacular facet of the astragalus, paralleling conditions in the calcaneum of Eiimetopias and differing in this respect from the cal- caneum of Odobenits on which these facets are united by a narrow isthmus. The proper allocation of disassociated skeletal elements is often puzzling, and occasionally uncertain, in case of closely related animals. The three calcaneal bones (Nos. 11589 and 11540, U. S. N. M. and 4314, C. A. S.) referred to females are lighter and less robust than those assumed to belong to males of Allodesmiis kernensis, but are otherwise quite similar. As compared with the calcaneum of larger individuals these tarsal bones are distinguished by having a more slender shaft, a narrower peroneal tubercle, and a less robust and more rounded greater process. The facets for articulation with other tarsal bones agree in all essential features with those on the calcaneum of larger individuals. Astragalus Inasmuch as the astragalus is the bone upon which the tibia and fibula rest, it transmits the weight of the body to the foot. The shape and relations of the astragalus with the tibia and fibula in turn indicate the extent to which the hind limbs may be used for progression on land. Corollary, and perhaps con- tributory, to the amount of rotation permissible, is the relative position of the fibular articular surface. The otariid type of astragalus permits the foot to be used for walking, while the phocid type of astragalus in conjunction with certain muscular Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 285 Left astragalus of Allodesmus kernensis, No. 4308, C. A. S., X 0.5. Fig. 53. Dorsal or anterior view. Fig. 54. Plantar or posterior view. relations restrict rotation and prevent the foot from being turned forward for progression on land. In many of its essential features, the astragalus of this fossil pinniped agrees with the odobenid type and it is there- fore not unlikely that this Miocene animal made use of its hind feet in progression on land. The neck is distinctly shorter than in Eumetopias jnbato. and the extero-lateral process of the body is less twisted. The dorsal surface of the body of this fossil astragalus (fig. 53) is provided with a saddle-shaped trochlea, as wide in front as behind, for articulation with the distal end of the tibia. The lateral borders of the trochlea are rounded and the posterior margin of the latter terminates at the level of the anterior margin of the astragalar foramen. The postero-superior border of the body is raised above the trochlea. In case of Odobenus divergens, the astragalus is furnished with a rather large astragalar foramen, but, in Eumetopias jubata. the foramen is rather variable in its occur- rence, and, when present, it is vestigial or incomplete. The astragalus of Odobenus differs from those of Eumetopias and this fossil pinniped in another feature, for it is furnished behind the outer half of the trochlea with a deep transverse groove for the flexor digit orum, which extends half way across the body and terminates on the posterior border of the external face about mid- way between the upper and lower margins of the lateral facet for the fibula. A very strong tendon would be required to produce a modification of this sort. 285 CALIFORNIA ACADEMY OF SCIENCES [Pnoc. 4th Sea. Over the external face of the body of the astragalus extends a large articular surface, which is convex above and concave below, for the distal end of the fibula. Distally, a crest-like margin defines the limits of this articular surface, and. anteriorly, it is continuous with the outer border of the trochlea. The distal or extero-lateral process of the body of the astragalus is somewhat everted. The internal face of the astragalus is excavated for the attachment of a ligament. On the posterior or plantar surface of the body (fig. 53) is an elongated concave ectal facet, which rests upon a cor- responding surface on the dorsal or anterior surface of the calcaneum. This articular surface resembles a boot in general outline, with the heel at the extero-superior angle of the body and the toe behind the astragalar foramen. In length and shape this ectal facet is more like that on the astragalus of Odohenus than on that of Eiimetopias. Internal to this ectal articular facet and crossing the bone from the external border of the neck to the inferior opening of the astragalar foramen is a deep furrow for the attachment of the interosseous liga- ment. This furrow also extends upward between the external prolongation of the body and the head, ending in a depression on the lower border of the trochlea. This astragalus is thus attached to the calcaneum in the same manner as in the living Odobenid?e and OtariidcT. The smaller elliptical sustentacular facet has a slightly convex curvature and its disto-internal margin is separated from the navicular articular surface of the head by a much narrower groove than is present in either Ennietopias or Odohenus. The astragali of Odohenus and of this fossil pinniped each ha\e a broad furrow, continuous mesially with that for the interosseous ligament, which crosses the neck between the sus- tentacular facet and the medial or internal tubercle. On the astragalus of Eiimetopias, however, the sustentacular facet is not separated from the medial or internal tubercle by a furrow. In proportion to the size of the body of the astragalus, the head is smaller than in Odohenus, but is not as noticeably flat- tened antero-posteriorly. Curiously enough the astragali of Eiimetopias and of this fossil pinniped have a deep pit for the attachment of a tendon on the anterior border of the articular surface for the navicular and the resulting indentation of this Vol.. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 287 s « e Mi.* 8 vjvqnf svttfopiun^ ■WN'STl 'L£SIZ -ON S1SU3UM1I snuis3pojjy •S "V O '90if -OK S1SU3UM2I snius^pojiY "S 'V 'O 'lift' 'ON sisu9UJ3if sntusgpojjy ■Q Tl '99iet -ON sisu3uj3i( sntusipoijY "S V "0 'ZOft' OM stsu3ui3i( snuisipojiY "S 'V '3 '80ft' -ON 'IPT CS) lO \0 "0 00 «— I r-i On O f> \0 O ro r*^ fO vjBqnC sm^ojaiun-^ ■IM-.M-S'A 'ZfSlZ -ON 00 On t^ "^ lO eg •* rq (N \0 \0 vO ■* ro <~0 vtvqnf svt^opum-g

* ■* su3Sx9nfp snu)qopQ 'Ijaq •WN-s'n'z^fsuoN O ^ O O t- u^ •^ PD OO CN On 00 vO lO vO (N O NO lO lO lO Tt< pNj (y^ \0 NO NO ■^ f^ NO ■* «0 lO NO O O O lO tN T* ■* CV) ■>* NO "0 4J C 4) c .2 ^ « SS TJ «M '^ rt • -; 1 ^ o s c3 g e o c "a o -l-a (A U] U3 S oS (U -t-> 4^ -^ rt rt c5 -t-> -*J CO nj -< O 00 •* CN vO rc l-~ O rc ro ■>* cvi r^i \C in O "* On >0 Cv r*^ r-1 >+ --' so i-~- 10 00 On •* '^ '-I rc ro •'l f~Ni On 00 l~^ J^ On t^ "^ -^ f<5 fO lO CnJ >* o. o o On 00 t^ fN rO "^v uo Cn) c H I/; Qi ■-o S O 05 c o 'S c :3 o o +J o ID it 0) T) 4-> ■i-' I/) IS; oJ rt fr, »-H cS -2 2 •'b^5 >* 00 oc VO rt< 0 No. ■ U.S. Ad. Eume Jul) 00 't tN 't Ov 'f -* ^ f^ rf (*> fN . -rf ir. fc t^ t^ 00 -* f^I 0 Ov fC 00 -+ 0 00 *-H 0 0 0 r^ 't<_-|.v ^ l^ t-- ^ rsj -H t- lO •* Tt* CN ro •>* *-H ,-H + OS rO 10 ■* 00 IT) »-i No. 4 C. A Lef Allode kerne vO t>- r^ J, d vO r^ -* -* r^i ro ^ ^-H ^H tn . >> ft a (T) vO 00 OC -rf fv) rf No. 4 C. A Lef Allode kerne oc c C^ d «-i U-l «+-i M-i ?i +J 4^ -kJ 4-) 0) <0 U Ol T^ 0 0 0 +J 1 (U a> 0) lU 'P. c I 6 S S £ 2;? C .2 2 .2 .2 c, -:: "C ■3 -S ■-o '-c .(-> -4- > -1- *-> +j -I-) 4-> cn y •/ t/3 (/) -y) r/; 0 4 ; i D D HJ HJ 4^ .^ > -^ ■*^ 4-> .^ -,-> cj c 1 c^ I rt oJ c3 ,-S 4J 1 * a a> K 41 0; in 1- . ;- :-i ii 1-. I- c c c C 0 a c 1 294 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. fer in that the slope of the proximal facet is more oblique and that of the distal facet is less oblique. The proximal concave articular surface for the mesocuneiform extends across the fibular face below the facet for the navicular and terminates at the proximo-plantar angle. This detail seems to charac- terize the entocunei forms of Odohcnus, Pontolis cf. niagnus,^^ and this fossil pinniped. Right entocuneiform of Allodesmtis kcniensis, No. 11546, U. S. N. M., X 0.5. Fig. 62. Dorsal or anterior view. Fig. 63. Internal view. The proximal end of the tibial or internal face (fig. 61) is furnished with a large oval-shaped facet for a sesamoid. Behind this facet the internal surface curves toward the plantar face. A club-shaped and saddle-like articular surface for the first metatarsal occupies the distal end of this tarsal bone. The facet on the proximal end for articulation with the navicular is more or less elliptical in outline and is shallowly concave. The dorsal surface is depressed and pitted as in Odohenus, but the plantar surface is more irregular and is furnished with a broad deep groove w^hich terminates at the disto-internal angle. The plantar face of this fossil entocuneiform bears a closer resemblance to the corresponding tarsal of Eitmetopias jiihata than to that of Odohenus dk'crgcns. Metatarsals 'I'he fifth metatarsal is represented by four bones of differ- ent sizes, ranging from medium to large, and all belonging to a right pes. They exhibit a surprising resemblance to the cor- responding metatarsal bone of Eumctopias juhata. The size, shape, and extent of the facets on the proximal end are essen- " R. Kellogg, Publ. 348, Carnegie Inst. Washington, 1925, pp. 107-108, text figs. 1314. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGIOyf 295 tially the same in both pinnipeds, but the fossil bones have a relatively wider, flattened shaft. As compared with the fifth metatarsal of Eitmetopias, the curvature of the proximal facet for the fourth metatarsal is much less concave, the facet for articulation with the cuboid has a much lower heel, and the enlarged proximo-plantar angle forms a rounded, inwardly directed protuberance. Fourth metatarsal bones from the right and left pes likewise agree in essential details with corresponding bones of Eume- topias juhata. The proximal end of the shaft is somewhat deeper and there is no constriction between the anterior and proximal facets for articulation with the fifth metatarsal. The shape of the proximal end of this metatarsal is similar to that of Eumetopias, but the articular surface is more convex and is continuous internally with facets for the head of the third metatarsal. A single third left metatarsal is included in the collection, and although the general contour of the proximal end is simi- lar to that of the same bone in Eumetopias juhata, it differs from the living sea lion in having an anterior, circular, concave facet and a relatively small posterior facet for articulation with the fourth metatarsal. The internal surfaces for articula- tion with the second metatarsal agree very closely with that of Eumetopias. Second metatarsal bones of at least three individuals are included in this lot of bones, three of which are from a right pes and a like number from a left pes. The anterior and posterior facets on the proximal end for articulation with the third metatarsal are separated by a rather deep groove. There is nothing to indicate that the second metatarsal articulated with the entocuneiform as in Eumetopias. The second meta- tarsal of Eumetopias has a large convex oval facet for articu- lation with a corresponding articular surface on the ento- cuneiform. These fossil metatarsals have anterior and pos- terior facets separated by a broad groove on the internal face of the head, but there is no indication of a corresponding sur- face on the entocuneiform. There is also a large, oval, con- cave surface below the posterior facet on the internal surface of the proximal end of the shaft. It would appear that these 296 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Seb. facets articulated with the first metatarsal which is not repre- sented in this collection. Measurements of Metatarsals (in millwveters) II C. A. 8. No. 4453 III C. A. S. No. 4450 IV C. A. S. No. 4448 V C. A. S. No. 4446 V U.S.N. M. No. 11861 Greatest length 89.0 30.4 16.7 12.5 22.0 87.+ 35.+ 21.0 16.9 98.0 41.5 21.8 15.7 22.8 93.+ 41.+ 25.8 14.8 Dorso-plantar diameter of head Transverse diameter of head. Narrowest transverse diame- ter of shaft 46.0 27.5 16.8 Transverse diameter of distal 7. Neotherium mirum-° Kellogg, new genus and species Type material: Right calcaneum, No. 11542, U. S. N. M. ; right astragalus, No. 11543, U. S. N. M. ; right cuboid. No. 11552, U. S. N. M.; left navicular. No. 11548, U. S. N. M. Referred speeimens: Right femur, No. 4300, C. A. S. ; left femur, No. 4549, C. A. S. ; right humerus, No. 4548, C. A. S. ; third metatarsal. No. 4464, C. A. S. ; phalanges, Nos. 4573, 4574, C. A. S. ; all from Sharktooth Hill, Kern County, Cali- fornia; Temblor; Miocene; Charles Morrice, Coll., 1924. Careful study of the pinniped material collected by Mr. Morrice has led the writer to conclude that at least two distinct types of otariids are present in the middle Miocene, Temblor fauna. This conclusion is based largely upon the structural peculiarities of the tarsal bones. The characters of the tarsal bones are quite constant in living pinnipeds and afford a means for identifying skeletal material. The differences observed between these bones and those referred to Allodesmus kernen- sis seem of generic value. Judging from the proportions of the skeletal elements that are known, this fossil pinniped was no larger and probably smaller than a female Zalophus cali- forniamis. " vtw, to swim; dtjpiop, wild beast. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGIOK 297 Humerus The fragment of the right humerus (No. 4548, C. A. S.) referred to this pinniped consists of the proximal half of the shaft, but the epiphysis, head, and portions of the deltoid crest are missing. The shaft is narrowed near the middle, arcuate in outline internally, and exhibits a very slight external curva- ture. The deltoid crest is quite thin and the anterior border does not fold over the external face of the crest as in Zalophus. Femur It is unfortunate that the right femur (No. 4300, C. A. S.) referred to this pinniped is badly damaged. The extremities are eroded, the shaft is fractured, and both condyles are miss- ing. A fragment of the distal extremity of a left femur (No. 4549, C. A. S.) of about the same size furnishes some addi- tional information concerning the external condyle and the patellar surface. The shaft of the femur (fig. 64) is rather slender, resembling that of Zalophus calif ornicus, but it is fractured traversely at the level of the lesser trochanter, and a section of bone in the region of the latter is missing. The curvature of the broken edges in this region indicates that the lesser trochanter was present. The greater trochanter is large and broad, and the intertrochanteric crest is not developed. The trochanteric fossa is large and quite deep, as is that of Allodcsmus, whereas in Zalophus the fossa is almost obliter- ated. It is obvious that the neck is rather long as compared with that of Zalophus, but most of the head is missing. The intercondyloid fossa is much longer than on the femur of Zalophus, but the patellar^ surface is quite similar. This fossil femur differs from those of Zalophus and Euine- topias in ( 1 ) the markedly greater transverse diameter of the proximal extremity; (2) the longer neck; and (3) the deeper trochanteric fossa. Measurements of the Femur Greatest length of shaft as preserved 136.5 mm. Greatest transverse diameter of proximal end (head to greater trochanter) 73.-|-mm. Least transverse breadth of shaft 31.8 mm. January 30, 1931 298 CALIFORNIA ACADEMY OF SCIEXCES [Proc. 4th Sea. 64 Fig. 64. Posterior view of right femur of Neotherium miruiii, No. 4300, C. A. S., X 1.0. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 299 Calcaneum In its general features this right calcaneum (No. 11542, U. S. N. M.) is somewhat similar to those of Arctocephalus australis (No. 217 ZS, U. S. N. M.) and Zalophus calif ornianus (No. 23332, U. S. N. M.). It differs from both, however, in having a more slender shaft, no groove on internal angle of proximal end of shaft, less expanded distal extremity, and no 65 Right calcaneum of Neotherium mirum, No. 11542, U. S. N. M., X 1.0. Fig. 65. Plantar or posterior view. Fig. 66. Dorsal or an- terior view. shelf below the sustentacular facet. The ectal facet (fig. 66) is narrow, curved from end to end, and distinctly raised above the shaft. The groove for the interosseous ligament is not sharply defined, but it is quite rugose. The sustentacular facet covers the dorsal face of the greater or internal process. The peroneal tubercle appears to be eroded and the question arises as to whether or not it was traversed by a vertical groove as in Arctocephalus or flattened as in Zalophus. The concave distal facet for the cuboid is rather small, but occupies most of the distal face of the shaft. Measurements of the Calcaneum Greatest length of shaft 52.8 mm. Greatest dorso-plantar diameter of distal end 16.8 mm. Greatest tibio-fibular diameter of distal end 28.2 mm. Greatest diameter of ectal facet 21.0 mm. 300 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Seb. Astragalus This right astragalus (No. 11543, U. S. N. M.) differs from the corresponding tarsal of Arctocephalus australis and Zalophus calif ornianus in having: (1) a deeper and more saddle-shaped trochlea; (2) a much shorter and less everted external prolongation of the body and consequently a less con- cave curvature of the fibular facet; (3) postero-superior por- tion of the body prolonged backward and raised above trans- verse groove between it and trochlea; (4) a relatively shorter neck; (5) a more convex distal facet for navicular; (6) a nar- row crescentic ectal facet; and (7) a shallower groove for interosseous ligament. Right astragalus of Neotherium minim, No. 11543, U. S. N. M., X 1.0. Fig. 67. Plantar or posterior view. Fig. 68. Dorsal or an- terior view. The lateral borders of the trochlea (fig. 68) are rounded and its posterior limits are sharply defined. Although the astragalar foramen is closed, its former position is marked by an irregular depression with numerous minute vascular fora- mina. The flattened fibular facet is somewhat longer than in either Arctocephalus or Zalophus. The crescentic ectal facet (fig. 67) is strongly concave and its lower edge is raised above the shallow groove for the interosseous ligament. In the mid- dle of this groove is the closed plantar orifice of the astragalar foramen. The sustentacular facet is slightly convex and its distal margin is cut off from the navicular facet by a .shallow tongue-like groove. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 39 1 Measurements of the Astragalus Greatest vertical diameter 39.0 mm. Greatest transverse diameter 32.0 mm. Greatest diameter of head 22.2 mm. Greatest diameter of ectal facet 21.8 mm. Greatest dorso-plantar diameter of body 26.6 mm. Navicular The small left navicular (No. 11548, U. S. N. M.) is rather long, relatively narrow, and quite thin. Differences in relative depth and in curvature of the articular surface for the astragalus distinguish this tarsal from those of Arctocephalus australis and Zalophus calif oniianus. A rather prominent tuberosity directed toward the fibular side arises from the plantar face. The elliptical facet for the astragalus (fig. 69) is strongly concave in all directions. This navicular lacks a distinct facet for articulation with the cuboid. The facets on the distal face (fig. 70) for the three cuneiforms correspond with those on the navicular of Arctocephalus australis. The larger one of these facets rests upon the entocuneiform and is separated from the smaller medial facet for the mesocuneiform by a raised ridge, and the latter in turn merges with the 69 70 Left navicular of Neothermm mirum, No. 11548, U. S. N. M., X 1.0. Fig. 69. Proximal view. Fig. 70. Distal view. obliquely placed facet for the ectocuneiform. Between the plantar tuberosity and the above mentioned facets is a rough- ened area for the interosseous lig^ament. Measurements of the Navicular Dorso-plantar diameter 18.9 mm. Tibio-fibular diameter 24.6 mm. Greatest vertical diameter 11.2 mm. 302 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Cuboid The right cuboid (No. 11552, U. S. N. M.) is relatively large and its configuration is more like that of Pontolis cf. niagmis-^ than that of any living otariid. On the proximal end of the cuboid is a large articular facet, curving obliquely for- ward and outward from the interno-plantar angle, which sup- ports the calcaneum. The extero-plantar angle of this facet Right cuboid of Neotherium mirum, No. 11552, U. S. N. M., X 10. Fig. 71. Dorsal or anterior view. Fig. 72. Plantar or pos- terior view. Fig. 7Z. Tibial view. is extended over upon the base of the prominent plantar tuber- osity. This facet is continuous internally with the sub-vertical concave facet for the astragalus. The postero-external tuber- osity is greatl}^ produced and its distal face is traversed by the sharply defined broad groove for the peroneus longus. A ridge-like internal continuation of this tuberosity (fig. 72) extends across the plantar face, but it diminishes rapidly in height. On the internal or tibial face (fig. 73) is a large proximal articular surface for the astragalus, navicular, and ectocunei- form. Two small facets for the ectocuneiform separated by a deep notch are likewise present on the distal border of the internal face. Distally there is a curved articular surface for the proximal ends of the fourth and fifth metatarsals, the facet for the fifth metatarsal being situated on the extero-plantar angle. " R. Kellogg. Structure of the flipper of a Pliocene pinniped from San Diego County, California. Publ. 348, Carnegie Inst. Washington, 1925, pp. 106-107, fig. 12. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGIO!^ 303 Measurements of the Cuboid Greatest proximo-distal diameter 34.3 mm. Greatest median dorso-plantar diameter 25.4 mm. Greatest tibio-fibular diameter 23.3 mm. Metatarsal The proximal end of a third right metatarsal (No. 4464, C. A. S.) is referred to this pinniped. It has a rather narrow facet for articulation with the ectocuneiform. On the extero- anterior ang^le of the head is a circular concave facet for arti- culation with the fourth metatarsal. The shaft is deeply exca- vated between the outwardly turned posterior angle of the head and the above described facet. There is a prominent convex articular surface for the second metatarsal on the anterior angle of the head. The shaft is rather slender and almost cylindrical below the head. Phalanges Two slender phalanges (Nos. 4573, 4574, C. A. S.) are thought to belong to this pinniped. The metatarsal and these two phalanges are similar in their proportions to the cor- responding bones of Callorhinus alascanus. The shorter of these two phalanges has an expanded distal extremity and may have been the middle phalanx of the first digit, while the other one tapers from the base to the extremity and corresponds in its proportions to the proximal phalanx of the fifth digit. One measures 50 mm. and the other 41 mm. in length. Order CETACEA Three species of cetotheres, a sperm whale, a shark-toothed porpoise, and nine other species of porpoises are recognized in the cetacean remains from the Temblor formation. This is the largest fauna of cetaceans thus far known for any forma- tion on the Pacific Coast of North America. One incomplete skull and the fragments of another skull show the stage of telescoping present in one of the cetotheres. Fragments of the cranium in addition to the ear bones indicate the presence of a second species. The third cetothere is known only from a single periotic bone. Other skeletal elements belonging to 304 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser, cetotheres are included in the collection. There are a number of incomplete bullae, in most cases the involucrum alone, which are not referred to any particular cetothere. Some of the limb bones are referred tentatively to these cetotheres, but no attempt has been made to allocate the incomplete and eroded vertebrae which unquestionably belong to one or another of these archaic whalebone whales. It is recognized that adequate material is not available to settle the relationships of many of the porpoises. It is suf- ficient, however, to indicate the presence of a number of dis- tinct species. The sperm whale is fairly well represented by skeletal elements, for we have the skull of an adult, portions of the skull of a young individual, and a number of ear bones. The new species of porpoises hereinafter described are based solely upon the periotics. since the writer has found that these ear bones are quite diagnostic. Mention is made of other skeletal elements belonging to odontocetes, and some of these bones are figured and described, although in most instances they are not referred to any particular porpoise. They are described merely as a matter of record and it is hoped that future collecting will provide the material for an adequate dis- cussion of the characters of the several species of porpoises represented in the Temblor fauna. Suborder Mysticeti Family CETOTHERIID-'E: Cetotheres At least three different kinds of cetotheres are included among the cetacean bones collected by Mr. Morrice at Shark- tooth Hill. A considerable portion of the skull, with the ear bones of the right side attached to it, forms the basis for one of these species; fragments of the hinder portion of the skull and the right periotic represent a second species ; and an im- perfect left periotic bone indicates the presence of a third species. Complete, as well as fragmentary cetothere limb bones of various sizes were sorted out of this collection. The bones of many kinds of fossil pelagic mammals were found scattered about in this bone bed, and it is unfortunate that none of the skeletal elements of the cetotheres were associated with skulls. Hence the allocation of these limb bones to any Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 3Q5 one of the above mentioned cetotheres may appear more or less arbitrary, but nevertheless they were critically compared with the corresponding bones of cetotheres found elsewhere and it is believed that the present disposition is as nearly accurate as one can hope to accomplish by using comparative measurements and other available data. Vertebrae of several sizes, and from different parts of the column, which undoubt- edly belong to cetotheres, were also obtained by Mr. Morrice. After some study it was decided to omit any discussion of these vertebrae because of the difficulty of allocating these bones with any degree of certainty to any particular species. Not one of the atlases fitted the condyles of the cetotheres herein- after described. Vertebrae, especially those from the cervical and caudal regions, of fossil porpoises exhibit a considerable range of variation, and it is not unlikely that those of the larger whales are equally, if not more, variable. The criteria employed for the classification of the mysticetes depend upon the relations of the bones which comprise the skull and before entering into a detailed discussion of these Temblor cetotheres it is desirable to summarize the diagnostic characters of the families Cetotheriidae and Balsenopteridae. Miller's opinions"- in regard to the diagnostic characters of the families Cetotheriidae and Balaenopteridae are in so close accord with my own that they are repeated to clarify the dis- cussion of the various genera, which are referred to these families. In both families the telescoping of skull is accomplished by a combined forward movement of posterior elements and a backward movement of anterior elements, which at least pro- duces some interdigitation of rostral and cranial elements. The nasals and ascending processes of premaxillaries are not situated entirely anterior to the level of the orbital wings of the f rontals ; and a definite ascending process of the maxillary is always present. In the Cetotheriidae the parietal is entirely behind the pos- terior level attained by nasals and ascending processes of maxillaries and premaxillaries; the occipital shield does not extend forward over level of orbit, or beyond anterior level attained by articular portion of squamosal; the frontal is 2=0. S. Miller, Jr.. Smithson. Misc. Coll.. vol. 76, publ. 2720, 1923, pp. 21-22. 305 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. broadly exposed on interorbital region : the expanded lateral (articular) portion of squamosal is relatively small, and its under surface is not deeply concave. The supraorbital process of frontal slopes gradually downward and outward from the level of the dorsal surface of interorbital region ; the parietals come in contact, or nearly so, on the vertex between the occi- pital shield and the frontal; the nasals are small (normal), their combined dorsal area equaling much less than half that of supraorbital portion of frontal : the rostrum tends toward breadth rather than depth ; the mandible is slender and con- spicuously bowed outward. In the Bal^enopteridas the parietal extends forward laterally beyond posterior level attained by nasals and ascending pro- cesses of maxillaries and premaxillaries ; the occipital shield extends forward over level of orbit and beyond the anterior level attained by the articular portion of squamosal ; the frontal is scarcely or not exposed on interorbital region ; the expanded lateral (articular) portion of squamosal is relatively large, its under surface being deeply concave ; the supraorbital process of frontal is abruptly depressed at base to a level noticeably below that of dorsal surface of interorbital region ; the rostrum tends toward breadth rather than depth : the man- dible is conspicuously bowed outward. In view of the present confusion prevailing in the applica- tion of generic names to fossil whalebone whales, it seemed desirable to fix the genotypes of those that include several species. In each instance, where it was necessary to fix the genotype from several species listed by the author when the generic name was propo.sed, a species founded upon a skull was chosen, if possible. Genotypes of Genera of Fossil Whalebone Whales Be- longing TO THE Families Cetotheriid.e and Bal^nopterid^ Middle Oligocene Pachycetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (3), vol. 6, No. 7, 1883, pp. 31-32. [Genotype, here designated as Pachycetus rohustus, Van Beneden, 1883 ; Rupelian stage ; "dans le couches phosphatees tres connues de Helmstedt (Bas Brunswick). — entre I'Elbe et le Weser. — un sable vert glauconifere" ; Museum fiir Mineralogie, Geologic und Vorgeschichte, Dresden, Germany.] Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION T^QJ Upper Oligocene Cetotheriopsis, Brandt, Bull. Acad. Imp. Sci. St. Petersbourg, vol. 16, 1871, p. 566. [Genotype, Balcenodon lintianus, Meyer, 1849; Aqui- tanian or I. Mediterranean stage; white marine sands in the vicinity of Linz, Austria. Stenodon, Van Beneden, 1865 (preoccupied), and Aulocetus, Van Beneden, 1875, have the same genotype as Cetotheriopsis; Museum Francisco-Carolinum, Linz, Upper Austria.] Lower Miocene Palceobalcena, Moreno, Rev. Mas. La Plata, vol. 3, 1892, p. 394. [Geno- type, Palceohalcena hcrgi, Moreno, 1892; Langhian Stage; Santa Cruz beds at Misioneros, Patagonia, Argentine Republic; Museum at La Plata.] Upper Miocene Cephalotropis, Cope, Science, n. s., vol. 3, 1896, p. 880; idem, Proc. x\mer. Philos. Soc, vol. 35, no. 151, 1896, pp. 141, 143-145. [Genotype, Cephalotropis coronatus, Cope, 1896; Yorktown formation (= St. Marys) ; probably from Chesapeake region, eastern United States ; United States National Museum.] Cetotheriomorphus, Brandt, Mem. Acad. Imp. Sci. St. Petersbourg (7), vol. 20, no. 1, 1873, pp. ii, 161-162, pi. 23, figs. 4-8. [Genotype, Cetotheriomorphus dubius, Brandt, 1873; locality unknown, possibly southern Russia; Museum of the Imperial Institute of Mines, St. Petersbourg.] Cetotherium, Brandt, L'Institut, Paris, vol. 11, no. 499, 1843, p. 241, and no. 502, p. 270. [Genotype, Cetotherium rathkii, Brandt, 1843; Sarmatian stage; Steppe limestone; Kertsch near promontory Takali, southern Russia; Museum of the Imperial Academy of Sciences, St. Petersbourg.] Eucetotherium, Brandt, Mem. Acad. Imp. Sci. de St. Petersbourg (7), vol. 20, no. 1, 1873, p. 143. [Genotype, here designated as Ceto- therium helmersenii, Brandt, 1873, op. cit., p. 95, pi. 6; Sarmatian stage ; limestone ; near^ the promontory Pekla on the coast of the Black Sea, Crimea, Russia; Museum of Imperial Institute of Mines, St. Petersbourg.] Herpetocetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 34, no. 7, 1872, p. 247. [Genotype, Herpetocetus scaldiensis, Van Beneden, 1872; Bolderien stage; sables inferieurs d'Anvers ; du nouveau canal d'Herenthals, troisieme section, partie de Stuyven- berg, environs of Antwerp, Belgium; Musee Royal d'Histoire Naturelle de Belgique, Bruxelles.] Isocetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 50, 1880, pp. 24-25. [Genotype, Isocetus De Pauwii, Van Beneden, 1880; Bolderien stage; sables; environs of Antwerp, Belgium; Musee Royal d'Histoire Naturelle de Belgique, Bruxelles.] 30g CALIFORNIA ACADEMY OF SCIENCES [Phoc. 4th Ser. Mesocetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 50, no. 7, 1880, pp. 22-23. [Genotype, Mesocetus longirostris, Van Beneden, 1880; Bolderien stage; sables; environs of Antwerp, Belgium ; Musee Royal d'Histoire Naturelle de Belgique, Brux- elles.] Mesoteras, Cope, Amer. Nat. vol. 4, 1870, p. 128. [Genotype, Mesoteras kerrianus. Cope, 1870; (?) Yorktown formation; marl, Quanky Creek, Roanoke River, Halifax County, North Carolina (possibly near town of Halifax, about 30 miles south of northern boundary of North Carolina, and south of towns of Roanoke Falls & Weldon) ; United States National Museum and the State Museum, Raleigh, North Carolina.] Metopocetus, Cope, Proc. Amer. Philos. Soc, vol. 35, no. 151, 1896, p. 141. [Genotype, Metopocetus durinasus, Cope, 1896; Calvert for- mation; marl near the mouth of the Potomac River, Maryland; United States National Museum.] Pachyacanthus, Brandt, Bull. Acad. Imp. Sci. St. Petersbourg, vol. 16, 1871, pp. 564-565 ; and idem, Mem. Acad. Imp. Sci. St. Petersbourg (7), vol. 20, no. 1, 1873, pp. 166-169, pis. 14-17. [Genotype, here designated as, Pachyacanthus suessii, Brandt, 1871 ; Sarmatian stage; Tegel von Nussdorf, Vienna basin, Austria; Naturhistori- schen Staatsmuseum, Wien, Austria.] Parietobalcena, Kellogg, Proc. U. S. Nat. Mus., vol. 63, publ. 2483, 1924, p. 1. [Genotype, Parietobalcena palmeri, Kellogg, 1924; Calvert formation ; greenish sandy clay ; 1 mile north Dare's wharf, Cal- vert County, Maryland; United States National Museum.] Rhegnopsis, Cope, Proc. Amer. Philos. Soc, vol. 35, no. 151, 1896, p. 145. [Genotype, Balana palceatlantica, Leidy, 1851 ; St. Marys forma- tion; City Point, Prince George County, Virginia. ProtohalcBna, Leidy, 1869 (preoccupied), has the same genotype; Academy of Natural Sciences of Philadelphia.] Siphonocetus, Cope, Proc. Amer. Philos. Soc, vol. 34, no. 147, 1895, pp. 140-141, pi. 6, figs. 3-5. [Genotype, Balcena prisca, Leidy, 1851 ; St. Marys formation; Westmoreland County, Virginia; Academy of Natural Sciences of Philadelphia.] Tretulias, Cope, Proc Amer. Philos. Soc, vol. 34, no. 147, 1895, pp. 143- 145, pi. 6, fig. 2. [Genotype, Tretulias buccaius, Cope, 1895: "York- town" ; possibly Maryland or Virginia ; United States National Museum.] VUas, Cope, Proc. Amer. Philos. Soc, vol. 34, no. 147, 1895, pp. 141-143, pi. 6, fig. 1. [Genotype, Ulias moratus. Cope, 1895; "Yorktown"; possibly Maryland or Virginia; United States National Museum.] Lower Pliocene Amphicetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 50, no. 7, 1880, pp. 20-21. [Genotype, here designated as, Amphicetus later, Van Beneden, 1880; Diestien stage; sables; environs of Ant- werp, Belgium; Musee Royal d'Histoire Naturelle de Belgique, Bruxelles.] Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGIOX 309 Cetotheriophanes, Brandt, Mem. Acad. Imp. Sci. de St. Petersbourg (7), vol. 20, no. 1, 1873, pp. 148-149, 156-157, pi. 20, figs. 13-16. [Geno- type, here designated as, Cetotherium (Cetotheriophanes) cuvieri, Brandt, 1873 = Balcena cuvieri, Fischer, 1829, Synopsis Mam- malium, p. 527; Plaisancian stage; mama argillosa cerulea; Monte Pulgnasco, Italy; Museo civico di Milano, Italy.] Heterocetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique (2), vol. 50, no. 7, 1880, pp. 21-22. [Genotype, here designated as, Cetotherium brevifrons, Van Beneden, 1872; Diestien stage; sables moyens d'Anvers, Belgium; Musee Royal d'Histoire Naturelle de Belgique, Bruxelles.] Megapteropsis, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 34, no. 7, 1872, p. 242. [Genotype, Megapteropsis robusta, Van Beneden, 1872; Diestien stage; sables moyens d'Anvers; Ecckeren and Wyneghem, near Antwerp, Belgium; Musee Royal d'Histoire Naturelle de Belgique, Bruxelles.] Notiocetus, Ameghino, Revista Argentina Hist. Nat., vol. 1, entrega 3a, 1891, p. 167, fig. 75. [Genotype, Notiocetus romerianus, Ameghino, 1891; Pontian; Pampean formation, Bahia Blanca, Argentine Republic] Plesiocetopsis, Brandt, Mem. Acad. Imp. Sci. St. Petersbourg (7), vol. 20, no. 1, 1873, pp. 143-146. [Genotype, here designated as, Ple- siocetus hupschii. Van Beneden, 1859; Diestien stage; sables; Saint Nicolas, environs of Antwerp, Belgium; Musee de I'Universite Catholique, Louvain.] Plesiocetus, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 8, no. 11, 1859, p. 139. [Genotype fixed as, Plesiocetus garopii by Van Beneden, 1872, Bull. Acad. Roy. Sci. Belgique (2), vol. 34, p. 242; Diestien stage; sables; Saint Nicolas, environs of Antwerp, Bel- gium; Musee de I'Universite Catholique, Louvain.] Middle Puocene Burtinopsis, Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. 34, no. 7, 1872, p. 246. [Genotype, Burtinopsis similis. Van Beneden, 1872; Scaldisien stage; sables; environs of Antwerp, Belgium; Musee Royal d'Histoire Naturelle de Belgique, Bruxelles.] Idiocetus, Capellini, Atti R. Accad. dei Lincei, Roma (2), vol. 3, pt. 2, 1876, pp. 12-13; idem, Mem. R. Accad. Sci. Bologna, (6) vol. 2, 1905, pp. 71-80, pis. 1-2. [Genotype, Idiocetus guicciardinii, Capel- lini, 1876; Astian stage; argilla turchina; Montopoli nel Valdarno inferiore, Tuscany, Italy; Museo di Geologia e di Paleontologia, Firenze, Italy.] Upper Pliocene Polaocetus, Seeley Geol. Mag., London, vol. 2, no. 8, 1865, pp. 54-57, pi. 3. [Genotype, Palaocetus sedgzvickii, Seeley, 1865; (?) Red Crag; Roswell Pit, in boulder clay of Ely, near Cambridge, England. (See Lydekker, Cat. Foss. Mamm. Brit. Mus., pt. 5, 1887, p. 31.) ] 310 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Something like 15 generic names have been proposed for fossil cetotheres from the upper Miocene, whereas but one species of lower Miocene age has been honored with a dis- tinct generic name. Turning to the Pliocene we find that the two families, Cetotheriidse and BaLnenopteridae, are represented by seven genera in the lower Pliocene, one in the middle Plio- cene, and two in the upper Pliocene, excepting of course those genera which have living representatives. The skull of the upper Oligocene Cefotheriopsis-^ is charac- terized in part by a high, narrow supraoccipital shield curving more forward than upward and divided mesially by a long vertical carina, elongate zygomatic processes not reaching for- ward to the level of the apex of the supraoccipital shield, and the vertex of the braincase, viewed from behind, being strongly depressed below the arching lambdoid crests. Of the 15 upper Miocene genera, the genotypes of six (Herpctocctus, Isocetiis, Rhec/iwpsis, Siphonocetus, Tretiilias, and Ulias) were based wholly or in part upon mandibles, the remainder of the skulls being unknown. Critical comments on the validity of tho.se that were founded on mandibles are given by Winge-* and True.-^ Vertebrae constitute the basis for the Austrian genus Pachyacanthits. The status of the Russian genus Cetotheriomorphiis is as doubtful as its specific name implies, for it was founded upon a single small lumbar verte- bra without epiphyses or neural spine. For the remaining genotypes portions at least of skulls were available to the original describer. Five species, rathkii, klindcri, helmersenii, priscuin, and mayeri were originally included in the subgenus Euceto- theriiim. Since rathkii is the genotype of Cetotheriuni, the species helmersenii may be selected as the genotype of Euceto- therimn, for it is the only one of the four remaining species which is based in part upon a braincase. The architecture of the skull, in so far as it is preserved, is not materially different from that of Cetotherium rathkii. In reviewing the literature, we find that the generic names Cetotherium and Plesiocetus »J. F. Brandt. Mem. Acad. Imp. Sci. St. Petersbourg, (7), vol. 20, no. 1, 1873, pi. 19, figs. 1-4. ** H. Winge, Vidensk, Meddel. naturhist. Foren. i. Kjobenhavn, 1909, pp. 1-37, pis. 1-2. =»F. W. True. Smithson. Misc. Coll., vol. 59. publ. 2081, 1912, pp. 1-8. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION ^\\ have been used rather indiscriminately for fossil whalebone whales of Miocene and Pliocene age, some of which unques- tionably belong in the family Balsenopteridse. Skulls of the Miocene genera Cetotheriiim, Cephalotropis, Mesocetus, Metopocetiis, and the Pliocene Amphicetus have a rather short intertemporal region, and the lateral lambdoid crests are continued through a short sagittal crest with anterior temporal crests which diverge anteriorly and gradually disap- pear on the base of the corresponding supraorbital process. The anterior limits of the temporal muscles on these skulls were sharply defined by these strong temporal crests. Winge^® obviously was mistaken in concluding that the skulls of all extinct finbacks have a temporal crest similar to that of Cepha- lotropis coronatus Cope, for there are quite a number, includ- ing Plesiocetopsis megalophysuni and ParietohalcBna palmeri, which either lack sharply defined temporal crests or do not exhibit any trace of them. In all of these fossil cetotheres the backward thrust of the mesial portion of the rostrum has car- ried the ascending processes of the maxillae and premaxillae, as well as the nasals, beyond the level of the preorbital angles of the supraorbital processes. Van Beneden^^ has already pointed out that the genus Ceto- thcriophanes was founded on an error in observation on the part of Brandt, for the scapula of the species cuvieri is muti- lated. The skull of the genotype, Balcena cuvieri, is exception- ally well preserved and presents all the diagnostic features of the family Balaenopteridae. The structural peculiarities of the skull do not warrant the retention of Brandt's generic name. Balsamo Crivelli^* apparently was the first author to place this species in its proper genus and it appears in his memoir as Baleen optera cuvieri. The genotypes of Megapteropsis and Burtinopsis are large species and appear to be related to the living humpback whale (Megaptera). The mandibular and cranial fragments, which formed the basis for Mesoteras kerrianus, are equal in size to the corresponding portions of the largest of the living fin- s' H. Winge, op. cit., p. 28. "P. J. Van Beneden. Bull. Acad. Roy. Sci. Belgique, (2), vol. 20. no. 12, 1875, r. i. =* G. Balsamo Crivelli, Gior. d' I. R. Inst. Lombardo Sci., Let. ed Arti, vol. 2, no. 9. 1842, pp. 133-138. 312 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. backs. Unfortunately a few fragments constitute all that is known of the skull of Idiocetiis guicciardinii, but the earbones are sufficiently diagnostic to show that this genus belongs in the family BalcTnopteridie. By employing this method of elimination in conjunction with diagnostic criteria, we find that there are three genera which should be critically examined to determine their relation- ships to the Temblor cetothere. These genera, so far as can be judged by the illustrations of skulls representing them, exhibit affinities, more or less close, with the Temblor ceto- there. The genotypes of two of these cetotheres, Heterocetus and Plesiocefopsis, belong to the lower Pliocene, but that of Pariefobalceiia comes from the middle Miocene. Bones found during the excavations for the gas reservoir north of the village of Saint-Nicolas. Belgium, in separate groups at a depth of 4 meters and almost at the level of the clay in the lower zone of the super-clayey quick sand, formed the basis for the three species, hupschii, burtinii, and garopii, which Van Beneden proposed to include in his new genus Plesiocetus. Some of these specimens were found on July 30. 1859, and the remainder a few days later. These specimens apparently were deposited in the museum of the Catholic Uni- versity at Louvain. Van Beneden stated that the species of Plesiocetus are distinguished from other whalebone whales by their free vertebras, by their having a scapula with a rudimen- tary coracoid process and well developed acromion situated high up and directed obliquely, and by a pyruliform tympanic bulla with an angular external surface. He also concluded that the skull suggests a whale with a more robust and less tapering head. This diagnosis, however, is based chiefly on species which were later excluded from the genus Plesiocetus. In 1872, Van Beneden-'' explicity stated that the generic name Plesio- cetus is retained solely for Plesiocetus garopii, a whale of large size and very close to the living Balcenoptera, and that the other originally included species are allocated to Ceto- therium. By this action. Van Beneden definitely fixed the species garopii as the genotype of Plesiocetus and all subse- "P. J. Van Beneden. Bull. Acad. Roy. Sci. Belgique, (2), vol. 34, no. 7, 1872, p. 242. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION T^\^ quent opinions of Van Beneden and others do not alter the status of Plesiocetns garopii. The present writer^*^ overlooked this action by Van Beneden and designated the type of Plesio- cetns as Plesiocetns hiipschii. It is interesting to note, however, that Van Beneden^^ in October, 1877, stated that the illustrations for the three species of Plesiocetns (garopii, hiirtinii, and hupschii) were prepared before the specimens in the museum at Brussels were put at his disposal, and that the study of this material had caused him to change some of his previous determinations. The volume dealing with the genus Plesiocetns^- appeared in 1885, and in it Van Beneden apparently reconsidered his previously published opinion and returned the species excluded in 1872 to the genus Plesiocetns, but he failed to mention what disposition was made of Plesiocetns garopii. It is apparent that the generic name Plesiocetns is not available for the group of cetotheres formerly associated together under this name. A year later when Brandt^^ published his memoir on the cetaceans of Europe, he concurred with the action of Van Beneden in 1872 and excluded all but Plesiocetns garopii from the genus Plesiocetns. In this memoir Brandt proposed a new subgenus, Plcsiocetopsis, for Cctotheriiim, and included in this new group Plesiocetns hnpschii, Cetotherinm hrevifrons, Ceto- theriuni dnbimn, Plesiocetns bnrtinii, and Plesiocetns gervaisii. One (Cetotherium brevifrons) of these five species was referred by Van Beneden"* in 1880 to the genus Heterocetus, and the present writer has selected this species for the type of that genus. Of the four species which remain, two alone (hnpschii and burtiiiii) are represented by adequate cranial material. The second (P. bnrtinii), orginally included in Van Beneden's genus Plesiocetns, is somewhat larger than P. hnpschii, having an estimated length of 5 meters. Van Bene- den states that he recognized portions of 4 individuals (axes) among the remains which formed the basis for Plesiocetns "0 R. Kellogg, Publ. 348, Carnegie Inst. Washington, 1925, p. 51. =' P. J. Van Beneden and P. Gervais, Osteographie des Cetaces, Paris, text, 1877, p. 612, footnote. '"P. J. Van Beneden, Description des Ossements Fossiles des environs d'Anvers. Pt. 4. Cetaces. Genre: Plesiocetus. Ann. du Mus. Roy. d'Hist. Nat. de Belgique, vol. 9, 1885, pp. 1-40, pis. 1-30. "J. F. Brandt, Mem. Acad. Imp. Sci. St. Petersbourg (7), vol. 20, no. 1, 1873, pp. iii, 165. "P. J. Van Beneden, Bull. Acad. Roy. Sci. Belgique, (2), vol. SO, 1880, p. 22. January 30, 1931 314 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4rH Skr. bnrtinii. No braincase was included among the co-types, and the complete list of specimens as given by Van Beneden is as follows : 2 squamosal bones, a nearly complete mandible, 2 tympanic bullae, atlas and axis (nearly complete) and 3 other cervicals. the first 3 dorsals, many lumbars, 3 caudals, many ribs, 2 incomplete scapulae, a humerus, and a radius. About 12 years later. Van Beneden^^ figured some of these specimens. Whatever disposition may ultimately be made of this species, much depends upon its relationships to specimens subsequently referred to it. Among the specimens described and figured in 1885 is the braincase*'' of a cetothere (Cat. No. 127) in the Royal Museum at Brussels. Van Beneden considered it to be an example of Plesiocetiis burtinii. This cranium is, therefore, a referred specimen and may or may not be identical with the original type material. It seems advisable, therefore, to select one of the other originally included species as the genotype of Plesio- cetopsis. Upon comparing the illustrations of the braincase of P. biirfinii with those of other cetotheres, it became apparent that the Belgian species is surprisingly like that of Parietobalcena pabneri in some respects. This resemblance is especially striking when the skulls are viewed from behind. Both skulls are characterized by the regular curvature of the lambdoid crests, by large postglenoid processes, and by small, wing-like exoccipitals. The periotic bones are quite unlike those of Parietobalccna. The precise relationships of Plesio- cetopsis burtinii will remain uncertain until the characters of the dorsal and ventral surfaces are determined. In so far as one can judge from available illustrations, this braincase dif- fers from the Temblor skull in the shape of the supraoccipital shield. In view of these facts, Plcsiocefus hupschii may be desig- nated as the type of Brandt's subgenus Plesiocetopsis, which is hereinafter raised to full generic rank. Portions of two skele- tons of a cetothere, whose length was estimated as being from 3 to 3_^ meters, formed the basis for Plesiocetopsis hupschii. Van Beneden specifically mentions a basicranium intact as far ^ p. J. Van Beneden and P. Gervais, Osteographie des Cetaces, Paris. Text, 1872, p. 284; Atlas. 1872. pi. 16, figs. 10-16. "P. J. Van Beneden, .\nn. Mus. Roy. d'Hist. Nat. Belgique, vol. 9, 1885, pi. 28, fig. 1; pi. 29, fig. 1. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGIOS 315 as the sphenoid, both condyles nearly complete, and a squamo- sal with a well preserved zygomatic process. The second speci- men consists of the occipital portion of the skull with con- dyles, and the corresponding portion of an atlas. This speci- men is said to belong to a slightly larger individual. Four or five vertebrae and fragments of ribs, belonging to an animal of the same size, are also mentioned. The basicranium was figured by Van Beneden,^^ and reference is made to this illus- tration by Brandt^* in 1873. The skull figured by Van Bene- den^® in 1885 is deposited in the Royal Museum at Brussels and bears the catalogue number 1239. The basicranium men- tioned in 1859, and figured in 1872. by Van Beneden is one of the co-types, and should not be confused with the Brussels museum skull, referred in 1885 to Plesiocetus hupschii. All comparisons hereinafter made are based on the co-type figured in the Osteographie des Cetaces. An outstanding peculiarity of the basicranium of Plesioce- topsis hupschii is the presence of a robust process with a large concavity in the area corresponding to the paroccipital process. Muscles arising from the atlas and thorax in recent balienop- terine whales are inserted upon the paroccipital process and adjoining surface of exoccipital bone. One might infer from analogous conditions in living mammals that these muscles had had tendinous insertions on this fossil skull. This, in turn, would seem to indicate that more freedom of movement was permitted to the head of this fossil whale than is the case in recent balaenopterine whales. Assuming that the basicranium of Plesiocetopsis hupschii, the exact dimensions of which were not published, was carefully depicted by the artist, there is no reason to suppose that it differed in any fundamental respect from the skull which Cope named Cetotherium megalophysum, for the relative proportions of the component parts are essen- tially the same in both species. These two skulls, however, differ from one another sufficiently to warrant their being referred to distinct species of the genus Plesiocetopsis. *' p. J. Van Beneden and P. Gervais, Osteographie des Cetaces, Paris, Atlaa, 1872, pi. 16, fig. 17. »J. F. Brandt, Mem. Acad. Imp. Sci. St. Petersbourg (7), vol. 20, no. 1, 1873, p. 144. ""P. J. Van Beneden, Ann. >lus. Roy. d'Hist. Nat. Belgiaue, vol. 9, 1885, pi. 21. fig. 1. 316 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. In the matter of relative proportions, the antero-posterior diameter of the temporal portion of each of these basicrania, as measured from the anterior mari^in of the squamosal in the temporal fossa to the posterior mar<;^in of the exoccipital, is nearly one-third greater than that of the Temblor skull. The skulls of the St. Marys and Belgian cetotheres have large con- dyles, the exoccipitals are extremely thick bones, and the posi- tion of the foramen ovale with respect to the temporal margin of the squamosal is approximately the same in both. Further- more, the periotic bones of these two fossil skulls have the same general type, and they exhibit a striking resemblance to the periotic of the Temblor cetothere. One analogous feature of the l)raincase of Heterocetus hrcvi- frons*" and the Temblor skull, is the height and extent of the forward thrust of the supraoccipital shield. If the restoration suggested by Van Beneden is correct, the apex of the supra- occipital shield projects forward beyond the level of the extremities of the zygomatic processes. The apical portion of this shield is smooth, apparently slightly depressed, and there is no indication of a vertical carina such as is found on the Tem- blor skull. I have been informed by A. Brazier Howell that this carina may suggest more differentiation of the muscles attached to the supraoccipital shield and possibly allow them more independent movement. The condyles of the Belgian skull are relatively large, the distance between their outside margins being equivalent to about one-fourth of the breadth of the skull across the zygomatic processes. The intertem- poral region is short and the sagittal crest appears to be some- what worn. The lateral extension of the exoccipital. the down- ward prolongation of the postglenoid process, and the curva- ture and development of a crest on the posterior margin of the squamosal are in close agreement with similar portions of the Temblor skull. One of the most obvious structural peculiari- ties of the Heterocetus hrevifrons braincase seems to have been overlooked by previous investigators, if the illustration used by Van Beneden has been correctly interpreted. There seems to be a deep fossa in the squamosal on the internal face of the zygomatic process above the glenoid articular surface. This «"?. J. Van Beneden, Ann. Mus. Roy. d'Hist. Nat. Belgique, vol. 13, 1886, pi. 2.S. fig. 1; pi. 26, fig. 1; pi. 27, fig. 1. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 3^7 fossa will be discussed more fully in a forthcoming paper on a cetothere skull from the Calvert formation of Maryland. This feature alone would remove any possibility of generic relationship with the Temblor cetothere. Parietohakena is the only Miocene genus, for which a skull is known, that is anywhere nearly contemporaneous with the cetothere from the Temblor formation hereinafter described, and both of these skulls lack shaply defined anterior temporal crests. In so far as our present knowledge goes, the Temblor skull is separable from Pavictohalcena by a combination of characters which may have no great importance. Aside from differences observable in the periotic bones of these two fossil cetotheres, the skull of Parietobalcena differs from the Temblor cetothere in having much more slender and more incurved zygomatic processes, a more triangular supraoccipital shield, prominent subhemispherical protuberances with obliquely placed concavity on lateral margins of the basioccipital, and exoccipitals with much thinner extremities. Our present knowledge of these small Miocene whalebone whales would seem to indicate that no generic name is avail- able for the Temblor cetothere which in some respects resem- bles Plesiocctopsis and in others Parietobalcena. 8. Tiphyocetus temblorensis''^ Kellogg, new genus and species Holotypc: No. 4355, ]\Ius. Calif. Acad. Sci. from Shark- tooth Hill, Kern County, Cal. ; Temblor, Miocene ; Charles Morricc, Coll., 1924. The type skull consists of an incomplete braincase in a fair state of preservation. The left side of the cranium, with its zygomatic process and the supraorbital processes of both frontals, is missing. Portions of the ros- trum were found associated with this braincase. The right tympanic bulla and periotic are attached to the skull. Referred specimens: No. 4357, C. A. S., portions of a dis- articulated skull in a fair state of preservation, the most im- portant pieces of this skull being the basicranium, the presphe- noid and posterior end of the vomerine trough, and the right squamosal region; No. 4425, C. A. S., condyles and basi- " Tivs, pilot of the Argo; kijtos, whale. 318 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. cronium; No. 4440, C. A. S., vertex of supraoccipital and sagittal portion of parietals ; No. 4439, C. A. S., both exocci- pitals, and fragment of basicranium with left pterygoid fossa ; No. 4353, C. A. S., right periotic; No. 4354, C. A. S., left periotic; No. 4356, C. A. S., right periotic; No. 11865, U. S. N. M., right periotic; No. 4438, C. A. S., incomplete left radius; No. 4388, C. A. S., proximal end of right ulna; No. 4436, C. A. S., proximal end of left ulna; No. 4442. C. A. S., incomplete sternum; No. 4373, C. A. S., incomplete left scapula; No. 4374, C. A. S., neck of right scapula; No. 4375, C. A. S., neck of right scapula; No. 4443, C. A. S., neck of right scapula; Nos. 4390, 4391, 4393, C. A. S., phalanges; Nos. 4376, 4378, C. A. S.. humeri. Skull In so far as the skull is concerned, this genus differs from Plesiocetopsis not only in the matter of the proportions of its component parts, such as wider temporal fossse and a shortened antero-posterior diameter of the squamoso-exoccipital region between the level of the bulla and the zygomatic process, but also in having a more externally placed foramen ovale and the extremity of the alisphenoid reduced in the outer wall of the braincase in the temporal fossa. In general form this braincase appears to be intermediate in some respects between Plesiocetopsis occidentalis (Kel- logg)*" and "Idiocetus" longifrons Van Beneden.*^ Of all the Belgian Miocene cetotheres, for which skulls are known, "Idiocetus" longifrons seems to exhibit the closest resemblance to the Temblor cetothere in the general conformation of the braincase. This upper Miocene species, however, exhibits no close relationship to the genotype, Idiocetus guicciardinii, from the upper Pliocene of Italy. The correct generic allocation of "Idiocetus'' longifrons is somewhat doubtful and may be held in abeyance until a general revision of related species is attempted. The parietals of this skull meet in the intertem- poral region to form a short sagittal crest, overspread the frontals in the interorbital region, and extend forward con- " R. Kellogg, Publ. 348, Carnegie Inst. Washington. 1925, pp. S0-S6, text figs. 7-10. "P. J. Van Beneden, Ann. Mus. Roy. d'Hist. Nat. Belgique, vol. 13, 1886, pp. 72-76, pi. 6.S; pi. 66, fig. 1; pi. 67, fig. 1; pi. 68. figs. 1-3. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 3^9 r"A \ \ \ \ Fig. 74. Dorsal view of incomplete skull of Tiphyocetus temhlorensis. No. 4355, C. A. S., X 0.25. siderably beyond the level of the posterior margins of the supraorbital processes. The frontals are narrowly exposed in the interorbital region between the anterior extremities of the parietals and the posterior extremities of the nasals, pre- maxillas, and maxillae. The anterior temporal crests, which in some species mark the anterior limits of the areas from which the temporal muscles arise, are either weak or absent entirely. When the skull is viewed from above the curvature of the posterior margin of the squamosal, the depression of the sur- face adjoining the zygomatic process, and the relative antero- posterior diameter of the body of the squamosal appear to agree with the corresponding portion of the Temblor skull, but the curvature of the anterior margin of the squamosal in the temporal fossa is quite different. On the basis of the illustra- tions which accompany Van Beneden's memoir it would appear also that the skull of "Idiocetus" longifrons differs from that of the Temblor cetothere in that the supraoccipital shield has a more constricted apex, the vertical carina is longer, the extero-inferior angle of the postglenoid process is acute and 320 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. not rounded, and the lateral protuberances of the basioccipital are ovoidal and not elongated. Dorsal viezc: The differential features of the Temblor skull are found in the architecture of the braincase (fig. 74). In contrast to the skull of Plcsiocctopsis megalophysnm (Cope), the extremity of the alisphenoid is reduced to a very small and narrow surface, the foramen ovale is placed nearer to the tem- poral edge of the squamosal, the temporal fossa as viewed from above is somewhat wider, the squamosal is shortened antero-posteriorly between the level of the bulla and the zygo- matic process, and the width of the skull across the exoccipitals and zygomatic processes is greater. Four skulls of a Calvert Miocene species of Pariefobalcuna, not designated at present by name because of our imperfect knowledge of a previously described cetothere from the same formation in Maryland, were available for comparison with the Temblor skull. They represent a species with a skull almost twice the dimensions of Parietohalccna palmeri. This cetothere had a wide temporal fossa, a broad basicranium, a squamosal shortened antero-posteriorly between the level of the bulla and the zygomatic process, a foramen ovale placed very close to the temporal margin of the squamosal, a basi- occipital with wing-like descending processes, and exoccipitals with very thin extremities. It differs from the ^femblor cetothere in having a different type of periotic, a basioccipital with wing-like processes instead of elongated lateral protuber- ances, a wider interval between the internal margins of the lateral processes of the basioccipital, slender, incurved zygo- matic processes, an exoccipital with a much thimier extremit)^ which is produced far below the level of the condyles, and much smaller condyles. The curvature of the postglenoid processes, on the other hand, is quite similar to that on the Temblor skull. The loss of the orbital portions of the supraorbital processes of the frontals of the Temblor skull prevents detailed com- parisons with some well known species, for their shape and direction, in addition to the contour of the temporal fossa, enable one to distinguish some species at a glance. At the base, each supraorbital process slopes gradually downward and outward from the median line of the post-narial region. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 32I but, in case of the living whalebone whales, these processes are abruptly depressed at the base. The frontals are excluded from the vertex of the intertemporal region, and their posterior bor- ders are overspread by thin plates of the parietals, although the latter terminate behind the level of the sutures which mark the position of the nasals and the ascending processes of the maxillae and premaxillae. These sutures also show that the basal portions of the nasal bones, as well as the ascending processes of the maxillae and premaxillae, were situated posterior to the rostral margin of the supraorbital processes. There is an emargination on each frontal for the reception of a nasal bone. The size and contour of the area occupied by the paired nasals shows that each of these bones was attenu- ated posteriorly. The parietals come in contact with each other on the vertex of the intertemporal region between the apex of the supra- occipital shield and the frontals, and are suturally united with the supraoccipital bone posteriorly and the squamosal inferi- orly. The sagittal crest is not as sharply defined on the type skull as on two other vertices referred to this species. Compared with Plesiocetopsis megalophysum, the supra- occipital shield of the Temblor skull is broader at the base and not quite so high. The lateral or lambdoid crests of the tri- angular supraoccipital shield are well developed. There is a well defined carina on the apical portion of this shield, on either side of which the surface is slightly depressed. The condyles project beyond the level of the exoccipitals. The squamosals and their zygomatic processes form the posterior and outer margins of the temporal fossae. The extremity of the right zygomatic process is missing and the external sur- face is eroded. The lambdoid crest is continuous inferiorly with a crest that curves forward and outward on the posterior margin of the squamosal. As in Plesiocetopsis mcgalophysum, the squamosal is strongly excavated below this carina. The fragments of the maxillas associated with this cranium do not exhibit any unusual peculiarities. Posterior viezv: From this aspect, the supraoccipital shield is seen to curve forward and upward : it is somewhat depressed in the center below the median carina on the apex. The exoccipitals are relatively small, coalesce with the supraoccipi- 322 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. tal above, and project outward and backward. Each exoccipi- tal is suturally united in front with the corresponding squa- mosal, and inferiorly it is fused with the basioccipital. The shape of the foramen magnum appears to be similar to that of Plesiocetopsis megalophysum, judging from the curvature of the internal margin of the right condyle. This condyle, how- ever, is quite different in general shape from that of the last mentioned cetothere. It is considerably narrower at the apex than at the base, convex from side to side and end to end, and is set off from the exoccipital by a shallow excavation. / ,/ Fig. 75. Ventral view of incomplete skull of Tifhyocetus temblorcnsis, No. 4355, C. A. S., X 0.25. Ventral vieiv: The median region of the basicranium (hg. 75), which is concave from side to side, is formed as usual by the basioccipital and basisphenoid. The posterior hori- zontally expanded plate of the vomer, which overspreads the basisphenoid, is destroyed on both specimens. The anterior margin of the basisphenoid is concave and it is separated from the presphenoid by an open transverse suture. Portions of the pterygoids remain attached to the lateral margins of the basi- sphenoid on the type skull, but their posterior extensions are Vol. XIX] KELLOGG— PELAGI C MAMMALS OF KERN RIVER REGION 333 destroyed. The latter contribute the internal walls of the pterygoid fossae and abut against the lateral protuberances of the basioccipital. These lateral protuberances are relatively smaller than those on the skull of Plesiocetopsis occidentalis. W'hen complete, these pterygoid bones bound the median 76 Fragment of skull of Tiphyocettis temblor ensis, No. 4357, C. A. S., X 0.5. Fig. 76. Ventral view of basicranium. 324 CALIFORNIA ACADEMY OF SCIENCES [Pboc. 4th See. 77 78 Fragments of skull of Tiphyocetus temblorensis, No. 4357, C. A. S., X 0.5. Fig. 77. Ventral view of vomer and presphenoid. Fig. 78. Proximal fragment of left maxillary. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 335 region of the basicranium and take part in the formation of the lower borders of the choanse. On the type skull, the right pterygoid is in contact with the supraorbital process of the frontal, meeting the descending wall of the optic canal near its orifice. The alisphenoid is hidden by the pterygoid, and its extremity is reduced to a nar- row strip in the temporal fossa. The roof of the pterygoid fossa is formed by the pterygoid. Behind this fossa is the large tympano-periotic recess. This recess is bounded by the squamosal externally, the exoccipital posteriorly, the basi- occipital internally, and by the alisphenoid and overlying pterygoid anteriorly. In the temporal fossa, the pterygoid is suturally united with the frontal and squamosal, and anteriorly it forms the posterior wall of the optic canal. The outer projection or zygomatic process of the squamosal is rather slender and flattened on its internal and external faces; the antero-internal portion of the squamosal is bifur- cated to provide an orifice for the large foramen ovale. The narrow lower branch or falciform process is suturally united Fragment of skull of Tiphyocetxis tcmhlorensis, No. 4357, C. A. S., X 0.5. Fig. 79. Posterior view of right exoccipital. 326 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Sf.r. with the pterygoid on the outer wall of the pterygoid fossa. The broad upper portion is likewise sutured with the ptery- goid. The curvature of the anterior or temporal margin of the squamosal is most pronounced in front of the glenoid region and corresponds in this respect to the skull of Plesio- cetopsis megalophysum. Behind the falciform process there is a distinct emargination for lodging Ihe anterior process of the periotic. The glenoid articular surface is rather wide and is concave antero-posteriorly. Behind this broad and rather Measurements of Skulls (in millimeters) Greatest breadth of skull across zygomatic processes, estimated Distance across skull between outside margins of exoccipitals, estimated Vertical height of skull (basisphenoid to apex of supraoccipital) Apex of supraoccipital shield to extero-inferior angle of exoccipital Outside margin of extremity of zygomatic process to apex of supraoccipital shield Antero-inferior margin oi foramen magnum to apex of supraoccipital shield Antero-inferior margin oi foramen magnum to notch between frontals at base of nasals Least breadth of cranium between temporal fossae . Breadth oi foramen magnum Greatest distance between outer margins of occipital condyles Greatest vertical diameter of right condyle Distance from antero-inferior margin of foramen magnum to anterior margin of basisphenoid Greatest distance across basioccipital between out- side margins of lateral protuberances Greatest depth of vomerine trough at anterior end of presphenoid Distance between tip of postglenoid process and tip of zygomatic process of right squamosal Apex of supraoccipital shield to notch betw-een fron- tals at base of nasals No. 43S7, C. A. S. ' As preserved. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 2)17 robust postglenoid process is a wide shallow channel for the external auditory meatus which commences at the postero- internal angle of the squamosal and curves outward. The apophysis or posterior process of the periotic is wedged in between the posterior face of the squamosal and the flattened exoccipital. The narrowing of the inferior edge of the ex- occipital resulted in a corresponding decrease in the area avail- able for the attachment of neck muscles. The posterior or lacerated foramen is continuous externally with the tympano- periotic recess and is continued backward across the exoccipital as a broad groove between the poorly defined paroccipital process and the corresponding lateral protuberance of the basioccipital. Periotic The periotic of this cetothere exhibits a surprisingly close resemblance to those of the St. Marys Plesiocetopsis niegalo- physmn (Cope), and the Scaldisian (middle Pliocene) Balcemila balcunopsis.** The periotics of these fossil whales exhibit the same side to side compression of the anterior process, but the periotic of Balcenula halccnopsis is distin- guished by its larger size, by the greater antero-posteriof diameter of the pars cochlearis and a larger cerebral orifice for the aqueduct of the cochlea. The bullae of both of these fossil whales are compressed from side to side and have a median longitudinal ventral ridge. It would probably be difficult, if not impossible today, to explain the association of the periotic figured by Van Beneden with the other skeletal remains of Balconiila balcFiiopsis. This right periotic lacks the posterior process, but the body is not much larger than that of the Temblor cetothere. As a whole this Belgian periotic is quite unlike any known member of the familv Balsenidae and the writer is inclined to suspect that it does not belong to balcsnop- sis. In so far as it is possible to make comparisons with the periotic of Plesiocetopsis megalophysum, it is practically iden- tical with that of the Temblor cetothere. In the Antwerp Basin during the Miocene and early Plio- cene there were at least three other species of fossil whales ** p. J. Van Beneden, Ann. Mus. Roy. d'Hist. Nat. Belgique, vol. 4, pi. 3, figs. 25-26, 1878. 328 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. \ \ Incomplete right periotic of Tiphyocetus temblorensis, No. 4353, C. A S., X 1.0. Fig. 80. Cerebral view. Fig. 81. Inferior view. with periotics similar to those of the Temblor cetothere, but the bulUe referred to these species are quite different. The periotic of the Diestian (lower Pliocene) "Idiocetiis" longi- frons*^ has a posterior process that closely resembles the cor- responding process of the Temblor periotic, and the relative size and position of the aqueducts of the cochlea and vestibule also agree, but a comparison of the cerebral views shows that the body of the former is deeper and more rounded, the anterior process is shorter, and there are differences in the relative positions of the entrance to the aqiiccductus Fallopii and the internal acoustic meatus. It is desirable to point out " p. J. Van Beneden, of. cit., pt. 5, vol. 13, 1886, pi. 67, figs. 2, 3, 4. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 329 46 here that the periotic of the genotype, Idiocetits guicciardinii, which belongs to the Astian (middle Pliocene) fauna of Italy, is so unlike the Belgian species that one might infer that the periotic of the latter either is erroneously associated with the other skeletal remains or else the generic allocation is incor- rect. The periotic of the Diestian Amphicetus later*'' has an exceedingly long and slender posterior process, a rather large pars cochlearis, and the cerebral orifice of the aqucediictus vestihuli opens into a groove. The periotic of the Diestien (lower Pliocene) Plesiocetopsis hupschii*^ has a much larger body, the outline of the combined anterior process and the body being distinctly triangular, and the cerebral orifice of the aqiiccduchis cochlece is larger, but the posterior process is not unlike that of the Temblor ceto there. The periotic (figs. 80, 81 ) of the Temblor cetothere possesses features which allocate the species in the group of small whalebone whales allied to Plesiocetopsis hupschii. The limits and diagnostic criteria for this group are rather indefinite at present and are likely to remain so until all known material is critically studied. It is unfortunate that so little attention was given to accurate methods of curatorial procedure at the time the specimens from the basin were passing through the hands of Du Bus, Van Beneden, their artists, and assistants. Portions of four periotics belonging to at least three dif- ferent individuals are the basis for the following diognosis. The posterior process (fig. 75) is elongate, attenuated at both ends, and relatively narrow. It is wedged between the ex- occipital and the squamosal, while the body and the pars cochlearis project into the large recess behind the pterygoid fossa. The posterior pedicle of the bulla is fused with the posterior process on the proximal end of the ridge which fol- lows the anterior border. Behind this ridge is the deep groove which marks the position of the facial nerve on its outward course. The external denser portion or body of the periotic is compressed from side to side, and its depth is fully one- fourth greater than its width. The external surface of the body is strongly convex and the internal surface is irregularly *' G. CapelHni, Balene Fossili Toscane, III. Idiocetus Guicciardinii. Mem. R. Accad. Sci. Bologna, (6), 1905, vol. 2, pi. 1, figs. 2, 3, 4. "P. J. Van Beneden, op. cit., pt. 5, vol. 13, 1886, pi. 1, figs. 1, 2, 3. *«P. J. Van Beneden, op. cit., pt. 4, vol. 9, 1885, pi. 21, figs. 2-7. January 30, 1931 330 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. excavated. The external surfaces of the body and anterior process are relatively smooth on two of these periotics, but are strongly rugose on the third. The pars cochlearis is small and not quite twice as long as broad; the ventral surface is convex and the external surface rises almost vertically from the inner margin of the fenestra ovalis. The internal outline of the pars cochlearis of the periotic here figured (fig. 80), viewed from the ventral side, is more strongly arched than on a second periotic (No. 11865, U. S. N. M.). The posterior face of the periotic is abruptly truncated above the circular fenestra rotunda. The fenestra ovalis is partially encircled by a very narrow rim and is sunk below the level of the channel for the facial nerve. A carina more distinct on one (No. 11865. U. S. N. M.), than on another (No. 4353. C. A. S.) separates the channel for the facial nerve from the fenestra ovalis. Small orifices of the semicircular canals can be seen at the bottom and on the outer wall of the vestibule. On one of these periotics (No. 11865, U. S. N. M.) there is a deep and narrow groove leading forward from the external rim of the fenestra ovalis to the notch between the pars cochlearis and the anterior process. This groove is much less distinct on the periotic here figured and does not extend backward beyond the level of the anterior pedicle of the bulla. The fossa for the stapedial muscle is broader than long and extends downward upon the internal face of the posterior process and the external face of the pars cochlearis. Bordering on the external margin of the epitympanic orifice of the aquceductns Fallopii (fig. 81) is a large shallow con- cavity for lodging the head of the malleus. The exact limits of this articular surface are not sharply defined and it appears to be continuous externally with the depression on the outer denser portion of the periotic. In front of this facet is the base of the slender anterior pedicle which supports the bulla. The fossa incudis appears to have been destroyed on all of these periotics. The anterior process is compressed from side to side and rather deep ; the extremity is emarginate on the periotic here figured and is straight on the others. Some of the most important features of this periotic are found on the cerebral face. Below the apex of the pars cochlearis is the internal accoustic meatus, at the bottom of Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 331 which is the spiral tract and a minute foramen singiilare. Because of its oblique position and the funnel-like shape of the meatus, the tractus spiralis foraminosus is largely hidden from a cerebral view. A high thick transverse crest separates the large entrance to the aqueduct of Fallopius from the more central!}' placed internal acoustic meatus. Posterior to the meatus is the small orifice of the aqueduct of the cochlea and above the latter is the large deep fossa into which the aqueduct of the vestibule opens. Between this fossa and the entrance to the aqueduct of Fallopius is a rather prominent projection. A large excavation is present on the cerebral face of the body above the entrance to the aqueduct of Fallopius. There is a broad deep groove on the posterior face, bordered on each side by distinct crests, which commences at the posterior mar- gin of the stapedial fossa and extends to the cerebral angle. The smooth convex surface of the pars cochlearis does not extend as far as the rim of the internal acoustic meatus and the irregular margin thus formed accentuates the jagged appearance of the cerebral face. Measurements of Periotics (in millimeters) Breadth of periotic at level of fenestra ovalis (from external face above ex- cavation to internal face of pars cochlearis) Greatest dorso- ventral depth of periotic (from most inflated portion of tym- panic face of pars cochlearis and ex- ternal excavation to most projecting point on cerebral face) Distance between epitympanic orifice of aquceductus Fallopii and tip of an- terior process No. 11865, U.S.N. M. Right 31.3 28.4 (1) No. 4353, C. A. S. Right 31.2 33.5 50.0 No. 4354, C. A. S. Left 51.0 No. 4356, C. A. S. Right 34.4 28.0 40.5 'Extremity of anterior process missing. 332 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Bulla The right tympanic bulla (fig. 75) attached to the skull is complete, and is characterized by the narrowness of the pos- terior end. The involuted portion of the bulla is depressed below the level of the overarching, thin, outer lip and decreases in thickness anteriorly. The dorsal surface of the involucrum is transversely creased and exhibits the usual convex undu- lation. The anterior pedicle is rather slender, and the posterior pedicle in cross section would appear "V"-shaped, with the apex behind. A narrow groove separates the posterior conical apophysis from the sigmoid process, and, in front of the latter, the thin outer lip is traversed in a vertical direction by a rather broad groove. The ventral profile shows that the bulla is depressed mesially. The ventral and external faces of the bulla form a continuous curved surface, but a fairly sharp angular crest separates the ventral and internal faces. The posterior end of the bulla is strongly attenuated. In contrast to the bulla of Plesiocetopsis megalophysiim, where the eustachian angle corresponds to the antero-internal angle, the eustachian angle of the bulla of the Temblor cetothere is placed mesially on the anterior border. The greatest length of this bulla is 87.8 mm., and that of the bulla of Plesiocetopsis megalophysiim is 94 mm. The bulla of the Calvert Miocene cetothere is considerably smaller, pleasuring less than 65 mm. in length. The greatest width of the Temblor bulla is 48.7 mm. and its depth at the level of the posterior apophysis is 52 mm. Scapula It is not improbable that the differences observed in the four incomplete scapulae (Nos. 4373, 4374, 4375, and 4443, C. A. S.) referred to this species are due to individual vari- ation. One (No. 4373, C. A. S.) of these is sufficiently com- plete to show the size and proportions of its component parts. The fan shaped blade (fig. 85) is rather high, with a regularly convex vertebral margin and an essentially straight posterior margin above the neck. The prescapular fossa is certainly very much reduced and may have been limited to the rather Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 333 82 83 Cervical vertebra of (?) Tiphyocetus temblorensis, No. 4400, C. A. S., about X 0.5. Fig. 82. Posterior view. Fig. 83. Lateral view. Scapulae of Tiphyocetus temblorensis, X 0.5. Fig. 84. Distal view of right scapula, No. 4375, C. A. S. Fig. 85. External view of left scapula, No. 4373, C. A. S. 334 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Sf.r. broad anterior face. The young of some species of recent fin- back whales have a scapula shaped like this fossil one, but in older individuals the vertebral margin is much less convex. The base of the acromion process is quite broad, but its length is uncertain. On this scapula most of the coracoid process is missing, but on one of the others (No. 4375, C. A. S.) the basal half of the long attenuated coracoid process, which arises close to the margin of the glenoid cavity is retained, and it is directed obliquely inward and downward. The glenoid articu- lar surface (fig. 84) on one of these scapulae (No. 4375, C. A. S.) is considerably expanded, the maximum diameters in the two directions being 101 mm. and 80 mm. The glenoid surface of the best preserved scapula measures 98 mm. and 66 mm. The greatest depth of the left scapula (No. 4373, C. A. S.) is about 240 mm., and the greatest width is esti- mated to be about 330 mm. It is difficult to make proper allowances for age without having a large series for com- parison, and, for the present, all four of these scapulae may be referred tentatively to this species. Fore Limb The remaining parts of the fore limbs of the Temblor ceto- there are not readily distinguishable from those of a number of Pliocene and Miocene cetotheres found elsewhere. In case of living whalebone whales, age differences are reflected in the bones of the fore limb, and limb bones without definite data are allocated correctly only with considerable difficulty. A corresponding amount of age and individual variation may be expected in these fossil cetotheres. The forearm of the Temblor cetothere is considerably longer than the humerus, and the ulna is longer than the radius. No carpal bones were noted, but a number of phalanges of various sizes which belong either to this species or to one of the other cetotheres hereinafter described were sorted out for comparison. The largest of these phalanges (No. 4390, C. A. S.) has a maxi- mum length of 81 mm. and a width of 56 mm. The smallest (No. 4393, C. A. S.) measures 57.5 mm. by 42.5 mm. There is nothing peculiar about any of these phalanges as they are all expanded transversely at their extremities and flattened in a dorso-plantar direction. \0l. xix] kellogg— pelagic mammals of kern river region 335 Humerus The general shape of the humerus of this cetothere is quite similar to the right humerus referred by Van Benedeh*" to Amphicctus rofimdus. The head and tuberosities on the proxi- mal end of the left humerus (No. 4376, C. A. S.) are eroded away, but the right humerus (No. 4378) is fairly well pre- served, with the exception of the greater tuberosity. The humerus of this cetothere has a large globular head and a prominent greater tuberosity, but the lesser tuber- osity is not as distinct as on a Calvert Miocene cetothere humerus. The large head is not set ofif from the shaft by a well marked neck, and the groove between it and the greater tuberosity is rather broad. Below this grove on the outer face of the humerus is a shallow and slightly roughened area for the infraspinatus muscle. The lower portion of the shaft is rather broad and is flattened in an extero-internal direction. The distal end is divided into two articular surfaces divided by a median crest. The upper surfaces of the radius and ulna are applied to these facets. The posterior profile of the humerus is strongly convex. A low protuberance on the antero-external angle of the shaft below the greater tuberosity modifies the anterior profile. The humerus of the Calvert Miocene cetothere has a large elongated fossa on the posterior face of the shaft about 18 mm. above the ulna face, but the Temblor humeri lack this fossa. It is possible that this fossa may mark the origin of one of the divisions of the triceps muscle, possibly the short head. Mra.-nirriiu'itfs of Ilmiicri (in »iilli)neters) Greatest length Extero-intemal diameter of distal end. . Antero-posterior diameter of distal end . Greatest diameter of head No. 4378, C. A. S. Right 243.8 61.0 109.5 96.0 "P. J. Van Beneden, Ann. :Mus. Roy. d'Hist. Nat. Belgique, vol. 13, 1886, pi. 17, figs. 4. 5. 336 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Radius The left radius (fig. 86) referred to this cetothere lacks the distal extremity. As is usual with these cetaceans, it has a rather simple form, and its curvature conforms to that of the shaft of the ulna. The shaft of the radius averages wider than that of the ulna. The external and internal surfaces of the shaft are convex, forming crest-like anterior and posterior margins. The maximum antero-posterior diameter of the shaft is 69.5 mm. and the maximum extero-internal diameter is 41.5 mm. The facet (fig. 87) on the proximal end for articulation with the humerus is flattened. There is also a well defined ulnar facet. 86 Incomplete left radius of Tiphyocetus temblorensis, No. 4438, C. A. S., X 0.5. Fig. 86. Internal view of shaft. Fig. 87. Proximal view. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 337 Ulna The proximal end of a right ulna (No. 4388, C. A. S.), and the proximal and distal ends of a left ulna (No. 4436, C. A. S.) are ascribed to this species. Their articular surfaces and proportions agree with the humeri described above. In general proportions, the shaft of the ulna (fig. 88) is not quite as slender as that of Heterocetns aflinis.^'^ Both of these ceto- theres have a well developed olecranon process projecting back- ward from the shaft of the ulna. The lower portion of the greater sigmoid cavity is considerably broader than the upper, and the articular surface of the former extends over upon the external face. The facet for the radius is broad and rather deep. The distal end of the shaft is expanded in an antero- posterior direction and flattened from side to side. The total length of the ulna when complete is estimated to be about 375 ■ S.V* f- Fig. 88. Internal view of right ulna of Tiphyocetus temblorensis, No. 4388, C. A. S., X 0.5. »» P. J. Van Beneden, Ann. Mus. Roy. d'Hist. Nat. Belgique, vol. 13, 1886, pi. 24, fig. 3. ^^g CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Skr. mm. ; the j^reatest diameter of the distal end is 87 mm., and the maximum extero-internal diameter of the lower portion of the irreater si<:moid cavity is 46.5 mm. Sterxu.m In view of the extraordinary variation which may be observed in sterna of recent whalebone whales, one should not attribute much importance to differences in general shape of these bones. True"'^ has figured 25 sterna of Balwnoptera physalits, many of which have quite unusual shapes. One or two bear a general resemblance to the sternum referred to the Temblor cetothere. particularly True's text figure 14. The sternum (No. 4442, C. A.'s.) of the Temblor cetothere is wider than long, with rather broad posterior arm or stem. The right wing of the broad anterior portion was broken off and no contact can be found between two pieces included in the collection. Nevertheless this sternum appears to have had the anterior border entire, with a medial vacuity or perforation below it, and with the wings scarcely S mm. long and 26.5 mm. wide at the base. A third phalanx (No. 4564, C. A. S.) is very slightly constricted, and it measures 55 mm. in length and 31 mm. in width at the ba.se. The other phalanges are broken and worn, and present no special peculiarities. " F. W. True, Description of a new fossil porpoise of the genus Delphinodon from the Miocene formation of Maryland. Journ. Acad. Nat. Sci. Philadelphia, (2), vol. 15, 1912, p. 184, pi. 25. tig. 4. Vol. XIX] KELLOGG—PELAGIC MAMMALS OF KERN RIVER REGION 357 Vertebr.^ Quite a number of odontocete vertebrae were collected by Mr. Morrice, but most of them are imperfect. The neural spines, transverse processes, and, in many cases, the neural arches as well are either tlamaged or missing. One series of 15 vertebrse consists of two dorsals (Nos. 4495, 4496, C. A. S.), one lumbar (No. 4497, C. A. S.). and twelve caudals (Nos. 4498 to 4509. C. A. S.). These verte- brae are considerably smaller than the corresponding vertebrae of Priscodelphinus at ro pins, and the centra are relatively longer. The dorsal vertebrae have the centra strongly con- stricted near the middle and the dorsal margins of both epi- physes are nearly straight. The largest dorsal (No. 4496, C. A. S.) measures 56 mm. in length and the height of the centrum posteriorly is 35 mm. The lumbar vertebra (No. 4497, C. A. S.) has broad transverse processes and an indis- tinct longitudinal keel on the inferior face. It is 68.5 mm. long and the height of the posterior face of the centrum is 41 mm. The five anterior caudals (Nos. 4498 to 4502, C. A. S.) have the transverse processes pierced basally by a foramen. Their neural canals are narrow and high, and progressively diminish in height. Large descending processes for articula- tion with the chevron bones are developed on the inferior sur- face at the posterior end of the centrum. The largest of these caudals (No. 4499, C. A. S.) measures 55.5 mm. in length, and the greatest height of the centrum posteriorly is 40.5 mm. Two smaller caudals (Nos. 4503 and 4504, C. A. S.) retain vestiges of the neural arches and possess a pair of longitudinal plate-like descending processes on the inferior surface of the centrum, but lack transverse processes. Five terminal caudals (Nos. 4505 to 4509. C. A. S.), varying in length from 28.5 mm. to 25.5 mm., lack a neural canal. The centrum of each of these caudals is pierced dorso-ventrally by paired verte- brarterial canals that open inferiorly into a deep longitudinal groove. Another series of five vertebrae (Nos. 4530, 4531, 4546, 4532, 4533, C. A. S.) have rather slender centra. This series includes four lumbars and one caudal. All of the lumbars have a prominent longitudinal inferior carina, on each side of which is a broad diagonal groove that extends from the 358 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. middle of the centrum to the posterior basal angle of the transverse process. Although none of these vertebrae has a complete neural arch, there is sufficient evidence to show that the neural canal was very narrow. The neural arches and transverse processes approximate the anterior margins of the centra. The single caudal vertebra (Xo. 4533, C. A. S.) has rather high neural arches, a low neural spine, and a very small neural canal. The transverse processes are largely destroyed, but were pierced basally by a foramen. The ventral surface of the centrum is eroded. The largest lumbar (No. 4546, C. A. S.) measures 58.2 mm. in length. Fifteen caudal vertebrje (Nos. 4510 to 4522, 4527, 4528, C. A. S.) are thought to represent still another type of por- poise. These caudals do not represent a continuous series and may have belonged to several individuals. The largest caudal (No. 4511, C. A. S.) measures 59 mm. in length and the smallest (No. 4522, C. A. S.) 25 mm. The larger caudals have their transverse processes pierced at the base by a fora- men. They possess large descending processes for the chevrons and have narrow neural canals. The caudals near the posterior end of the series have very low neural arches, the neural canal is nearly closed, and the neural spine is very low. With one exception, all of these caudals lack vestiges of the transverse processes. These caudals possess a pair of longitudinal plate-like descending processes on the inferior sur- face of the centrum. The three small terminal caudals (Nos. 4520 to 4522, C. A. S.) have a pair of thick longitudinal ridges on the inferior surface of the centrum. Four badly eroded lumbar vertebrae (Nos. 4523 to 4526, C. A. S.) differ from those heretofore described in having more robust centra, although the largest of these vertebras hardly measured more than 65 mm. in length when complete. Among the remaining miscellaneous vertebrae are six which belong to a much smaller porpoise than any of those heretofore mentioned. A small dorsal vertebra (No. 4534, C. A. S.), about 30 mm. in length, has the centrum contricted mesially. It lacks all of its processes. A posterior dorsal (No. 4539. C. A. S.) referred to the same porpoise is likewise incomplete. It measures 43.5 mm. in length. On the four lumbars (Nos. 4538, 4537. 4536, and 4540, C. A. S.), the longitudinal Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 359. inferior carina progressively increases in depth. The length of the largest No. 4538. C. A. S.) of these lumbars is 48 mm. and the smallest (No. 4540, C. A. S.) is 41 mm. All of these vertebrae have rather slehder centra. A single small caudal vertebra (No. 4541, C. A. S.) has a high neural spine, small neural canal, and short transverse pro- cesses. The centrum has deep concavities above and below the transverse processes. It measures 35.5 mm. in length, and the distance from the tip of the neural spine to the inferior surface of the centrum is 51.5 mm. Fragments of an atlas (No. 4543, C. A. S.), two axes (Nos. 4544, 4545, C. A. S.), and the centrum of a cervical vertebra (No. 4542, C. A. S.) belong to some small porpoise. In addic- tion to the foregoing vertebrae, there is a rather large caudal vertebra (No. 4529, C. A. S.) which indicates the presence of a porpoise of about the same proportions as Priscodelphinus atropius. Key to Periotic Bones of Porpoises From the Temblor Formation, Sharktooth Hill, Near Bakersfield, California 1. Extremity of anterior process resembles the handle-end of a crutcli, when viewed from in front; between the fenestra ovalis and the deep concave fossa for the head of the malleus is a narrow cres- centric excavation which commences near the epitympanic orifice of the aqumductus Fallopii and extends downward upon the external face of the pars cochlearis; the large egg-like accessory ossicle is firmly ankylosed to the ventral face of the anterior process; postero-intemal angle of ventral facet on posterior process, when complete, reaches to the level of internal margin of stapedial fossa; cerebral face of outer denser portion of periotic nodular; greatest antero-posterior diameter of pars cochtearis 20 mm. or more Aulophyseter morricei (p. 361) Extremity of anterior process either pointed, rounded, or abruptly truncated; greatest antero-posterior diameter of pars cochlearis less than 20 mm 2 2. Extremity of anterior process (an tero- ventral angle) attenuated and pointed ,.'.... 3 Extremity of anterior process rounded, or abruptly' truncated and compressed from side to side 4 3. No incisure on posterior face above and internal to stapedial fossa; anterior process swollen; entrance to aqueduct of Fallopius con- stricted; cerebral and external faces of outer denser portion of periotic form a continuous smooth convex surface; internal acous- 360 CALIFORMA ACADEMY OF SCIENCES [Proc. 4th Ser. tic meatus cucurbital in outline; transverse diameter, excluding posterior process, 24-26 mm Squalodon errahundus (p. 373) A deep incisure on posterior face above and internal to stapedial fossa; apical portion of anterior process on ventral face grooved longi- tudinally to support outer lip of bulla; groove for facial nerve sinks below level of external rim of fenestra ovalis; entrance to aqueduct of Fallopius constricted; transverse diameter, excluding posterior process, less than 21 mm Liolithax kernensis (p. 375) 4. A subtriangular flattened or depressed area on cerebral face behind internal acoustic meatus, the apex of which is occupied by the fossa inclosing the cerebral orifice of the aqueduct of the vesti- bule; a pit is usually present on the posterior face above the stapedial fossa 5 Not as in preceding, and with orifice of aqueduct of vestibule in closer proximity to rim of internal acoustic meatus 7 5. Anterior process with longitudinal carina on cerebral face; groove for facial nerve does not sink below level of external rim of fenestra ovalis; posterior face of posterior process concave above ventral facet; a low crest is present on antero-external border of ventral face of pars cochlearis opposite to the facet for the accessory ossicle 6 Anterior process without longitudinal carina on cerebral face: pars cochlearis strongly inflated posterior to aqueduct of cochlea; a deep pit on posterior face above stapedial fossa; stapedial fossa bounded internally by a thin-edged crest; a well defined crest is present on antero-external border of ventral face of pars cochlearis opposite to the facet for the accessory ossicle. CE(fo/;7/ia4r mira (p. 378) 6. Triangular depressed area behind internal acoustic meatus sharply defined, with apex produced beyond fossa inclosing cerebral orifice of aqueduct of vestibule Lamprolithax simulans (p. 381) Triangular depressed area behind internal acoustic meatus less sharply defined and with apex not produced beyond fossa inclosing cere- bral orifice of aqueduct of vestibule. La w/^r«///Aa.Y annectens (p. 383) 7. Greatest diameter of periotic (tip of anterior process to apex of ventral facet on posterior process) more than 25 mm 8 Greatest diameter of periotic (tip of anterior process to apex of ventral facet on posterior process) less than 25 mm.; cerebral face of outer denser portion of periotic flattened ; entrance to aquceductus Fallopii constricted; no pit is present on pcisterior face above stapedial fossa Nannolithax gracilis (p. 386) 8. Cerebral face of outer denser portion of periotic broad, distinctly flattened and depressed external to internal acoustic meatus, and general plant of this surface forms a right angle with the external surface; a subcorneal swelling posterior to cerebral orifice of aqueduct of cochlea; no pit is present on posterior face above stapedial fossa; facial canal sinks below level of external rim oi fenestra ovalis Platylithax robusta (p. 388) Cerebral face of outer denser portion of periotic convex, with the outer two-thirds more or less flattened 9 Vol. XIX] KELLOGG^PELAGIC MAMMALS OF KERN RIVER REGION 35^ 9. Outline of internal face of anterior process as viewed from the cerebral side distinctly convex ; posterior face of posterior process rounded or flattened above ventral articular facet 10 Outline of internal face of anterior process as viewed from the cerebral side nearly straight; a pit on posterior face above stapedial fossa; posterior face of posterior process excavated and concave above ventral articular facet Loxolithax sinuosa (p. 390) 10. Antero-extemal border of ventral face of pars cochlearis traversed by a low crest; a pit or slit-like depression is present on posterior face above stapedial fossa Grypolithax pavida (p. 396) Antero-extemal border of ventral face of pars cochlearis smooth, without any trace of a crest; posterior face deprvissed above stapedial fossa, but no pit is present .... Grypolithax obscura (p. 393) Family PH YSETERID^ : Sperm Whales 1 1 . Aulophyseter morricei Kellogg'® Type specimen: No. 11230, Division of Vertebrate Paleon- tolog}', U. S. Nat. Mus. The type consists of a skull in a fair state of preservation. The supraorbital process of the left frontal and overlying maxilla, the left lachrymal and jugal, and the extremity of the rostrum are missing. Four enamel- crowned teeth and a right periotic were found near this skull. Paratype: Portions of the skull (No. 11313, U. S. N. M.) of a young whale or embryo were found about 20 feet from that of the adult. Referred specimens: Right periotic. No. 10853, U. S. N. M. ; right periotic, No. 2794, C. A. S. ; right periotic. No. 2795, C. A. S. : left periotic. No. 2796, C. A. S. ; right periotic, No. 2797, C. A. S. ; right periotic, No. 2798, C. A. S. ; left periotic. No. 2799, C. A. S. ; right periotic. No. 2800, C. A. S. ; right periotic. No. 2801, C. A. S. ; (?) mandibular teeth, Nos. 2802, 2803, 2804, 2805, 2806, 4575, 4576, C. A. S. The skull (fig. 106) is especially interesting, for it demon- strates that the reduction of the maxillary dentition had com- menced as early as the Middle Miocene. The top of the skull has been adjusted to lodge a fat or spermaceti cushion, and, in correlation with this peculiar structure, the relative proportions and relations of the bones forming the dorsal surface have " R. Kellogg, Study of the skull of a fossil sperm whale from the Temblor Miocene of southern California. Publ. 346, Carnegie Inst. Washington, 1927, pp. 1-23, pi. 1-9. January 30, 1931 362 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ssr. been altered to form a large supracranial basin. The dorsal cranial elements are markedly asymmetrical and the left narial passage is much larger than the right. Skull About four feet in length ; distal constriction of rostrum coextensive with the shallow, closely approximated, alveolar grooves; no trace of distinct or vestigial alveoli for lodging- teeth in the upper jaw ; a large maxillary incisure and a smaller posterior maxillary foramen ; more or less flattened, broad, pre- maxillaries forming the dorsal surface of median portion of rostrum and shallow supracranial basin; right premaxillary expanding behind narial passages into a broad thin plate which is applied to upper surface of frontal and overlaps the maxillary along its internal margin ; left premaxillary turned out of its course by enlargement of the corresponding narial passage and apparently terminated near posterior margin of this passage; premaxillaries forming extremity of rostrum; maxillary relatively thick posterior to antorbital notch and forming lateral wall of supracranial basin; supracranial basin limited posteriorly by transverse crest of supraoccipital and continued laterally to elevated portion of maxillaries ; post- narial portion of right maxillary not meeting the left in the middle line; left narial passage much larger than the right; tapering zygomatic processes placed rather far forward ; short temporal fossa ; parietal excluded from vertex of skull ; two orifices for infraorbital system on ventral face of maxillary; lachrymal narrow, firmly lodged between maxillary and supra- orbital process of frontal, and fused with broad jugal which does not project much more than half way across orbit; palatine bones large, broad, and not projecting forward beyond anterior margins of anterior infraorbital orifices; pterygoids with large hamular processes ; falcate processes of basioccipital projecting beyond level of condyles; a deep jugular incisure; alisphenoid thin, large, expanded horizontally, bounded anteriorly by supraorbital process of frontal, suturally united posteriorly with squamosal, and in contact with anterior sur- face of exoccipital : no tympano-periotic recess ; optic canal confluent with sphenoidal fissure; foramen ovale pierces basal portion of alisphenoid; large jugulo-acoustic canal. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 353 Max. Inc. \Ap.max. ^S.or.pr, p. max.f. Ex. oc. Fig. 106. Dorsal view of skull of Aulophyseter morricei, restored, No. 11230, U. S. N. M., X H- 364 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Measurements of Skull (in millimeters) Total length, as preserved (condyles to tips of pre- maxilla>) Total length, as estimated (condyles to tips of pre- maxilla;) Length of rostrum, as preserved (antorbital notches to extremity) Total length of rostrum, as estimated (antorbital notches to extremity) Breadth of rostrum at antorbital notches, as restored. . Breadth of rostrum at swelling in front of antorbital notches, as restored Greatest breadth of skull across supraorbital processes, as restored Greatest breadth of skull across zygomatic processes of squamosals Vertical height of skull (basioccipital to transverse crest) Vertical height of skull (hamular process of pterygoid to transverse crest) Vertical height of rostrum at base (at level of antor- bital notches) Greatest width of right maxilla from a ventral view (inside margin to apophysis) Greatest length of right premaxilla, as preserved .... Greatest breadth of right premaxilla at level of nares . . Greatest breadth of right premaxilla posterior to nares. Least breadth of right premaxilla in front of antorbital notches Greatest antero-posterior diameter of supraorbital process of right frontal at extremity Greatest thickness of preorbital portion of supraorbital process of right frontal Elevation of lateral crest of supracranial basin above orbit Least breadth of supraoccipital between temporal fossie Distance from summit of transverse crest to upper margin oi foramen magnum Height oi foramen magnum Breadth oi foramen magnum No. 11230, U. S. N. M. Adult No. 11313. U. S. N. M. Young 1114.0 1210.0 712.0 800.0 558.0' 595.0' (725.0^ 748. 0» 354.0 360.0 490.0 718 0 298.0 + 443.0 + 177 0 363.0 988.0 210.0 121.0 197 0 82.0 113.0 137.0 40.0 74.+* 100.0* 250.0 480.0 133. + 78.0 95.0 ' Estimated. • Anteriorly. « Posteriorly. ' Inner border missing. ' Left. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERM RIVER REGION 355 Measurements of Skull (in milUmeters) No. 11230, U. S. N. M. Adult No. 11313. U. S. N. M. Young Greatest distance between outside margins of occipital condyles 248.0 158.0 96.0 700.0 493.0 204.0 780.0 238.0 135.0 293.0 185.0 198.0 75.0 107.0 198.0 110.0 30.0 86.0 162.0 48.0 85.0 Greatest vertical diameter of left condyle Greatest transverse diameter of left condyle Distance across skull between outer margins of exoc- cipitals Distance between anterior margin of apophysis of supraorbital process of right frontal and posterior margin of right condyle Distance across basicranium between foramina ovale . . Total length of vomer Greatest length of left palatine Greatest breadth of left palatine Greatest length of left pterygoid Greatest length of hamular process of right ptervgoid. Greatest transverse diameter of right lachr>'mal Greatest antero-posterior diameter of right lachrymal. Greatest length of right jugal 151.0^ 68.55 62 4- Greatest length of right zygomatic process Greatest breadth of right alisphenoid at extremity. . . Greatest depth of right alisphenoid at extremity Least distance between optic canal and foramen ovale . . Least distance between optic canal and jugulo-acoustic canal Greatest diameter of left respiratory passage 24.0 49.0 ' Left. Teeth Crown covered with smooth enamel in front and on one side, but wrinkled on opposite side; enamel of crown passes into cement without any perceptible increase or decrease in diameter or neck ; root long, backwardly curved, and broadly oval in cross section ; pulp cavity closed. Periotic None of the periotic bones here discussed was attached to a skull, and were it not for the fact that only one type of physe- teroid periotic was represented among the many specimens 366 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. obtained from a short trench dug in the uppermost horizon of the Temblor formation, there might be some question as to their allocation. Eight right and three left periotic bones of this physeteroid were obtained at the one locality. It is remarkable how closely, except for minor modifications in the anterior process, these periotics resemble those of recent sperm whales, for the relative proportions and peculiarities of the various structures are essentially the same. As in other Right periotic of Aulophyseter morricei, No. 2795, C. A. S., X 0.75. Fig. 107. Cerebral view. Fig. 108. Inferior view. sperm whales, the periotic may be dixided for purposes of description into a very dense external portion, the combined anterior and posterior processes, a lighter internal sub- hemispherical pars cochlearis and the pars vestibularis. Minor variations in the contour of the articular facet on the posterior process are observable in the eleven periotics under considera- tion, but most of them may be attributed to the effects of erosion. There are fine osseous crests on the tympanic face of the posterior process which are arranged like rays radiating from a common center on the internal margin. This articular facet is irregular in outline, the posterior margin rather evenly curved, and the external and anterior margins more or less sinuous. The major portion of the posterior facet is concave, but the anterior border slopes obliquely to the groove for the external auditory tube. The ventro-internal border of this process projects inward and the free edge contributes the floor of the facial canal for approximately one-half of its length. The external face of this process is flattened and more or less Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGIOX 357 rugose. According to the text figure and photographs the right and left periotics reproduced in the memoir by Abel,^^ and which are unfortunately allocated to Eurhinodelphis longirostris, it is evident that the distal or external portion of the posterior process is distinctly emarginate and rugose. There is very little variation in the general outlines of the pars cochlcaris (fig. 108). as seen from a ventral view, in these eight periotics. Whatever differences are observable are of a minor nature. There is a low, short crest or nodosity near the middle and on the internal border of the pars cochlearis on nine of these periotics. which may have resulted from contact with the involucrum of the tympanic. The major portion of the ventral face of the pars cochlearis is more or less flattened and slopes toward the anterior margin, with the most inflated point opposite to the fenestra oralis. The external face is flat- tened and nearly vertical. From a tympanic view, three aper- tures are visible, and. of these, the largest is the fenestra rotunda on tlie posterior face of the labyrinthic region. This fenestra is crescentic in outline, with a rounded nodosity above which partially closes the opening. The fenestra ovalis is ovoidal in outline and is situated near the center of the tym- panic face of the periotic. A narrow rim which is raised above the canal for the facial nerve and the fossa for the stapedial muscle encircles the fenestra on the outside. The foot plate of the stapes completely fills the fenestra. A medium sized interna] passage, which leads from the vestibule, and a pair of minute antero-external foramina, leading to the semi- circular canals, also open into the vestibule. The minute aque- duct leading from the foramen singulare opens near the bot- tom of the vestibule on the internal wall and near the anterior angle. The epitympanic orifice of the aquceductus Fallopii and the fenestra ovalis lie in a depression, although the former is largely concealed from a ventral view by the projecting ledge of the fossa inciidis. Posterior to this orifice, the facial canal is open along its whole length, sloping obliquely down- ward and curving around the posterior face of the posterior process. Posteriorly, the facial canal borders on a large semi- enclosed fossa for the stapedial muscle. The fossa for 'the " O. Abel, Les dauphins longirostres du Bolderien (Miocene superieur) des en- virons d'Anvers. Mem. Mus. Roy. d'Hist. Nat. Belgique, vol. 3, 1902, pj). 121-12J, text fig. 19; pi. 17, figs. 11-12. 358 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Stapedial muscle is a deep concavity and the surface for the attachment of the muscle extends downward upon the external face of the pars cochlearis. A thin-edged crest is developed on the ventro-external angle of the labyrinthic region by the encroachment of the fossa for the stapedial muscle. This thin curved crest, which rises behind the sta- ])edial fossa, has been destroyed on eight of these periotics, including that associated with the type skull, but is well pre- served on three. Between the fenestra ovalis and the deep concave fossa for the head of the malleus, there is a narrow crescentic excavation which commences near the epitympanic orifice of the aqiiceductus Fallopii and extends downward on the external face of the pars cochlearis to its tympanic face. Between the rounded tuberosity or swelling on the anterior process and the anterior border of the articular facet on the posterior process, the ventral surface of the external denser portion of the periotic is hollowed out. becoming distinctly grooved as it approaches the fossa incudis. On seven of these periotics the fossa incudis is preserved in its entirety, but it has been damaged on the periotic associated with the type skull. This small shallow elliptical fossa is situated at the extremity of the thin ledge which projects inward below the facial canal. The fossa incudis receives the cms hreve of the incus. The extremity of the anterior process resembles the handle end of a crutch when viewed from in front. This peculiarity is produced by two projecting points, the external and internal angles. There is a crease, more distinct on some than on others, on the posterior face of the tuberosity external to the epitympanic orifice of the aquccductus Fallopii. The external face of the anterior process is rounded off between this tuberosity and the apex of the process. Anterior to the fossa for the head of the malleus, the ventral surface of the anterior process is deeply concave from end to end and more or less flattened from side to side. The relatively large accessory ossicle or unciform process of the tympanic is lodged in this fossa. Accessory ossicles were present on all eleven of these periotics. The accessory ossicle is relatively large, almost egg- shaped, with a longitudinal groove marking the line of anky- losis with the external lip of the tympanic, and fusing with the anterior process of the periotic along its posterior and Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERS' RIVER REGION 359 external margins. If this ossicle is forcibly removed, small portions of the corresponding surface of the anterior process break away with it. \Mien the accessory ossicle is in position, it contributes the outer wall of the deep notch between it and the pars cochlearis. Most of the depressions and nodosities observed on the denser external portion of the cerebral face of the periotic do not appear to have any deep seated significance. Four of these periotics have a rather prominent pyramidal tuberosity arising external to the orifice of the aquceductus vestihuli and three do not exhibit any trace of this nodosity. On two there is a large nodosity external to the entrance to the aquwductus Fallopii. On all of these periotics a broad groove, irregular in appear- ance because of the presence of small nodosities, traverses the anterior process in front of the pars cochlearis. From a cere- bral view the posterior process appears rather slender and the anterior process very robust ; the pars cochlearis is inclined forward. An irregular crease defines the limits of the pars vestibularis and the posterior process on the cerebral face of the periotic. The pars vestibularis is relatively small ; its external surface is concealed by the anterior and posterior pro- cesses, and internally it is continuous with the pars cochlearis. A rather instructive example of how slight changes in the growth of a bony partition between the entrance to the aquce- ductus Fallopii and the more centrally placed tractus spiralis foraininosus can modify the contour of the internal acoustic meatus is shown in these eleven periotics. The internal acous- tic meatus of the periotic (fig. 107) used for illustration repre- sents the average type. In the majority of these periotics the rim of the internal acoustic meatus is pyriform in outline. In others a thin partition or transverse crest is interposed between the entrance to the aquceductus Fallopii and the fossa bounding the spiral tract. The outer edge of this transverse crest is almost continuous with the rim of the meatus and imparts a distinctly ovoidal outline to the latter. The largest and most external of the orifices which appear on the cerebral face is that of the aquceductus Fallopii, which pierces the substance of the periotic and through which passes the facial nerve to emerge on the tympanic face slightly anterior to the fenestra ovalis. Internal to the entrance to the aquceductus Fallopii is 370 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. + 1 ^M^ra •-< t~~ CN o o j^ •S "V "3 '1082 -ON fO o t^ lO 00 00 e^ rr) »-< C^ »-H ^^ + ^H^l'S. o lo r^- O >0 t^ S V 3 '0082 -ON t^ r^i — i 00 — " d r^ •* r-i tN tN r^ ^^ «-H lO vo -+ S V 3 '66U ON o> 5M3ra 00 t^ r~ <>I S 'V '3 '16U -ON Ov 00 t^l *M3i^ o fN 00 O r^ -; S V "3 'f6tZ oM lO o vO \0 1^ C^ r-1 'T) ^ (N -^ '"' n^m »0 o O f^ fN LO "S V 3 'S6i2 OM 00 r-i t— 00 O ,— I tN •+ ■^ rs r^ f^l + 'M^i-a — O O -^ fO c ■S "V '3 'SbLZ ox >o t^ 0-. vO 00 d cs "^^ ^ fV) — ' rs WSiX o + + lO ^ o "-J •JVNSn 'fSSOl ON vO ^ 0> 0^ C~l „ fN •* -H fV) fN r^ (adXi) iiiSi-y CN - O 00 + 00 n NSn 'OlTll OM ID 00 -< vO Os 00 fN t3 T3 o "^-^^ a o 'c re .5 ^--^ o tj c c c y, (u , a. -4^ o ^ ^ X2 XI y2 aj rtj ii; o o ii u2 tn w ff) o O Q Q a 1 Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERW RIVER REGION 2,7\ the deep internal acoustic meatus, on the bottom of which is the tractus spiralis foraniinosus and the minute foramen cen- trale. On the external wall of this meatus and about half-way between the rim and the bottom is a small compressed foramen singnlare. A relatively thin partition or transverse crest, whose outer margin may or may not be depressed below the level of the rim of the internal acoustic meatus, places the ori- fice of the aqiiceductus vestihiili outside of and posterior to the meatus. This orifice is compressed and opens into a slit-like fossa. The cerebral orifice of the aqiiceductus cochlecc is con- siderably larger than that for the aqiiceductus vestihuli, and the interval between these orifices varies from 2 to 3.8 mm. Radius Two radii that lack the distal end of the shaft are referred to this fossil sperm whale. They correspond in shape with those of Physeter catodon and differ from those of all known cetotheres. Each radius has a thin proximal epiphysis com- prising the articular surface for the humerus. This articular surface is rugged and is flush with the external or lateral margin, but slopes abruptly to the internal margin. The hemi- Proximal end of right radius of (?) Aulophyseter morricei, No. 4444, C. A. S., X 1.0. Fig. 109. External view. Fig. 110. Proximal view. in CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. circular facet for the ulna at the proximal end of the posterior face is depressed mesially. The shaft is flattened from side to side. The facet for the humerus on the largest radius (No. 4445, C. A. S.) measures 74.4 mm. antero-posteriorly and 54 mm. transversely. The same measurements for the smaller radius (No. 4444, C. A. S.) are 68 mm. and 48.5 mm., respectively. Proximal end of right radius of (?) Aulophysctcr morricei, No. 4445, C A. S., X 1.0. Fig. 111. External view. Fig. 112, Proxi- mal view. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 373 Family SOUALODONTID^ : Shark-toothed Porpoises The two ear bones hereinafter described are referred to the genus Sqitalodon, for reasons which are almost indefinable, and yet all known squalodonts have similar peculiarly shaped periotics. The subtile characters that distinguish the periotics of squalodonts from those of other porpoises are apparent to Left periotic of Sqitalodon errabundus. No. 11573, U. S. N. M., X 1.0. Fig. 113. Inferior view. Fig. 114. Cerebral view. anyone who has studied these bones, although it is difficult to point out any tangible feature which will invariably identify them. This appears to be the first published occurrence of a representative of this family in Tertiary deposits on the Pacific Coast of North America. Remains of squalodonts have been found in Australia and New Zealand. 12. Squalodon errabundus^^ Kellogg, new species Holotype: Left periotic, No. 11573, Division of Vertebrate Paleontology, U. S. Nat. Mus. from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Morrice, Coll., 1924. Aside from the loss of the posterior process, the type peri- otic is exceptionally well preserved. Both processes are broken off on a second left periotic (No. 11574, U. S. N. M.) referred to this species. Very little variation can be observed in corresponding parts of these two periotics. Diagnosis: Viewed from the ventral side (fig. 113) the pars cochlearis is convex, although it is depressed opposite the fenestra ovalis, and the posterior face slopes abruptly to the cerebral margin above the large fenestra rotunda. The narrow ** Errabundus, wanderer. 374 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. external rim of the fenestra oralis is not complete and is depressed below the chaimel for the facial nerve. The epi- tympanic orifice of the aquetluct of Fallopius is relatively small. A portion of the stapedial fossa and most of the g-roove for the facial nerve extend over upon the missing pos- terior process of the type periotic. The fossa for the stapedial muscle is deep, rather small, and extends downward upon the outer wall of the pars cochlearis; it stops anteriorly at the nar- row external rim of the fenestra oTalis. A sharp-edged crest is developed on its internal margin. It is possible that the second periotic may be abnormal in one respect, for the abo\e mentioned sharp-edged crest, which forms the inner border of the stapedial fossa, is appressed posteriorly to the posterior process, forming an aqueduct through which the facial nerve passed in its outward course. No recent or fossil porpoise, known to the writer, has a periotic modified in this manner. The excavation on the outer denser portion of the periotic between the posterior process and the tuberosity is very narrow and deep. The narrow projecting ledge, on which the fossa incudis is situated, is damaged on both periotics. Between the pointed extremity and the constriction in front of the tuber- osity, the anterior process swells out on the cerebral side, forming a large protuberance. On the internal side of the narrow tuberosity is a large concavity for lodging the head of the malleus. Some of the distinguishing features of the periotic of this porpoise, as compared with that of Squalodon calve rtensis,^^ are the position of the fossa inclosing the orifice of the aqua;- ductus z'estibitli, the shape of the anterior process, the relative size of the pars cochlearis, and the cucurbital outline of the internal acoustic meatus. A low broad transverse crest (fig. 114) separates the large entrance to the aqueduct of Fallopius. from the more centrally placed fossa for the tractus spiralis foraminosiis. The foramen centrale pierces the transverse crest at its external angle. Outside and external to the internal acoustic meatus is a deep fossa into which the aqueduct of the vestibule opens. The small circular orifice of the cochlea is equally distant from the rim of the meatus. The cerebral and external faces of the outer denser portion of the periotic form " R. Kellogg, Proc. U. S. Nat. Mus.. vol. 62, publ. 2462, 1923, text fig. 3, and pi. 8, fig. 6. •Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 375 a continuous smooth convex surface, imparting the charac- teristic shape to this ear bone. Measurements of Periotics (in viillimeters) No. 11573, U. 8. N. M. Left (type) No. 11574, U. S. N. M. Left Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) Greatest dorso- ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between epitympanic orifice of aquceductus Fallopii and tip of anterior process 24.0 15.0 Family DELPHINID^ : Porpoises 13. Liolithax kernensis"" Kellogg, new genus and species Holotype: Left periotic, No. 4340, Mus. Calif. Acad. Sci., from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Morrice, Coll., 1924. Paratype: No. 11565, Division of Vertebrate Paleontology, U. S. Nat. Mus. Left periotic of Liolithax kernensis. No. 4340, C. A. S., X 1.0. Fig. 115. Cerebral view. Fig. 116. Inferior view. •" Xtioj, smooth; Ai&a^, diminutive of Xt^os, a small stone, in allusion to the dense periotic bone; kernensis, the Kern River region. T^y(^ CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Diagnosis: Four left periotics are known for this species, two of which belong to the CaHfornia Academy of Sciences and two to the United States National Museum. One of the specimens in the California Academy of Sciences is imperfect and somewhat worn. In general, the periotic of this porpoise seems to be characterized by the direction of the facet on the ventral face of the posterior process, by the pro- longation of the antero-ventral angle of the anterior pro- cess to support the outer lip of the bulla, by the transverse crease on the ventral surface of the anterior process which marks the anterior limit of the tuberosity, by the presence of a deep incisure on the posterior face above and internal to the stapedial fossa, and by the constriction of the entrance to the aqnccductus Fallopii. The ventral facet of the posterior process is badly worn on all four of these periotics, but it is most nearly complete on the one here figured (fig. 116). This facet slopes from the apex to the base and is shallowly concave ; the ventro-internal mar- gin is raised and the postero-internal angle overhangs the groove for the facial nerve. The posterior and external faces of the posterior process form a continuous curve. The lyars cochlearis is relatively smaller than in Platylithax rohusta, and externally it rises more abruptly from the fenestra ovalis. The fenestra rotunda is circular in outline and produces a slight indentation, although the pars cochlearis is not noticeably inflated in the region of the aqueduct of the cochlea. The rim of the fenestra ovalis is very narrow, but the raised border which separates it from the channel for the facial nerve, and the fossa for the stapedial muscle is rather broad. Within the vestibule can be seen the small orifices of the semicircular canals and the terminal opening of the foramen singulare. The epitympanic orifice of the aquceductiis Fallopii is placed above the antero-internal angle of the fossa for the head of the mal- leus, and the channel for the facial nerve leading backward from it is sharply defined anteriorly, but posteriorly its mar- gins become rather indistinct. The fossa for the stapedial muscle encroaches internally upon the pars cochlearis, resulting in the formation of a crest posterior and external to the fenestra rotunda. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 377 The fossa incudis (fig. 116) for the cms breve of the incus is very narrow and occupies a thin ledge. Externally a thin carina separates this fossa from the excavation on the outer denser portion of the periotic between the posterior process and the tuberosity. The anterior process is furnished with a pointed tongue-like process which projects inferiorly beyond the rounded extremity. On three of these periotics the ventral surface of this pointed process is grooved longitudinally to provide additional support for the outer lip of the bulla. The accessory ossicle of the bulla rests on the ventral surface of the anterior process between the pointed extremity and the tuber- osity at the base. The concavity for lodging the head of the malleus has a slight indentation on its external border which is associated with the crease which marks the posterior limit of the tuberosity. The elongate internal acoustic meatus (fig. 115) is the most prominent structure on the cerebral face. This meatus is Measurements of Periotics (in millimeters) No. 10854, U.S.N. M. Left No. 4340, C. A. S. Left (Holotype) No. 4341, C. A. S. Left No. 11S6S, U.S.N. M. Left Breadth of periotic at level of fenestra ovalis (from external face above ex- cavation to internal face of pars cochlearis) 18.2 20.2 19 7 Greatest length of periotic (tip of ante- rior process to tip of posterior process) 29.5 + 31.8 + 30.+ 30.8 + Greatest dorso- ventral depth of peliotic (from most inflated portion of tym- panic face of pars cochlearis and ex- ternal excavation to most projecting point on cerebral face) 13.3 12.8 12.0 12.8 Distance between fenestra rotunda and tip of anterior process 20.5 22.0 21.8 Distance between fenestra rotunda and tip of posterior process 12.5-f 14.7 + 14.2 + Distance between epitympanic orifice of agticeductus Fallopii and tip of an- terior process 17.2 18.5 16.8 18.0 January 30, 1931 378 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. strongly constricted along the entrance to the aquceductits Fal- lopii, and behind this constriction its walls descend obliquely to the kidney shaped fossa which is occupied by the tractus spiralis foraininosus. A low partition separates this fossa from the entrance to the aqueduct of Fallopius. On three of these periotics, the slit-like foramen singulare is situated on this transverse bony crest, but on the fourth (No. 10854 U. S. N. M.) it is placed near the level of the spiral tract. The cerebral orifice of the aquccductus vcstibiili opens into a deep triangular fossa and the small circular orifice of the aqueduct of the cochlea is placed much closer to the rim of the internal acoustic meatus. The cerebral and external faces of the outer denser portion of the periotic form a continuously curved sur- face, without any irregularities. The anterior process, as viewed from the cerebral side, is rather robust and convex. 14. CEdolithax mira*'^ Kellogg, new genus and species Holotype: Right periotic, No. 11572, Division of Verte- brate Paleontology, U. S. Nat. Mus. from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Mor- rice. Coll., 1924. Paratypc: Left periotic, No. 11571, Division of Vertebrate Paleontology, U. S. Nat. Mus. Right periotic of CEdolitlwx mira. No. 11572, U. S. N. M., X 1.0. 117. Cerebral view. Fig. 118. Inferior view. Fif Diagnosis: The periotics referred to this porpoise are in some respects larger replicas of those referred to Laniprolithax siniulans. Attention is directed to the pronounced inflation of the pars cochlearis posterior to the aqueduct of the cochlea, to the depression whose apex is formed by the fossa inclosing the orifice of the aqueduct of the vestibule and wdiose base is the "otSew, to swell, to become swollen; Ai0a^, dimunitive of XiOos, a small stone in allusion to the dense periotic bone; mira, strange, wonderful. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 379 outer rim of the internal acoustic meatus, to the rather deep pit on the posterior face above the stapedial fossa, and to the antero-posterior diameter of the pars cochlearis. The margins of the ventral facet on the posterior process (fig. 118) of the type periotic are worn and the posterior half, at least, of this process is missing on the paratype periotic. In so far as can be determined from these two specimens, this facet is concave on the basal half, rather wide, and is furnished with a few grooves radiating outward from the raised ventro- internal margin. Viewed from the ventral side, the pars cochlearis is most strongly inflated in front of the fenestra rotunda, slightly depressed opposite the fenestra oralis, and slopes toward the anterior and inner margins. A low crest is also present on its antero-external border. The fenestra rotunda is crescentic in outline and the surface is depressed behind it. The outer narrow rim of the fenestra ovalis is im- complete and no carina intervenes between it and the more elevated channel for the facial nerve. In the narrow vestibule are the usual orifices of the small semicircular canals. The channel for the facial nerve, which leads backward from the epitympanic orifice of the aquceductus Fallopii, is rather broad and appears to terminate at the postero-internal angle of the posterior process. The deep elongate fossa for the stapedial muscle extends forward to the narrow external rim of the fenestra ovalis and is bordered on the internal side by a sharp- edged crest. The fossa incudis is destroyed on the type periotic. On the parat}^pe periotic, the fossa incudis is rather small, elliptical in outline, and is raised above the rather narrow and deep exca- vation on the outer denserportion of the periotic. The anterior process is robust and is bluntly truncated at the extremity. On its ventral surface is the usual mesially elevated cordiform facet for the accessory ossicle of the bulla. The posterior out- line of the tuberosity is convex on both periotics, but the type differs from the paratype in having a deep transverse crease on the posterior face of the tuberosity and a corresponding notch in the fossa for the head of the malleus. Direct comparison of these two periotics with the six peri- otics referred to Lamprolithax simidans revealed some minor differences. The shape of the internal acoustic meatus varies 380 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. in both species. On the type periotic of CEdolithax mira (fig. 117), the entrance to the aqueduct of Fallopius is constricted anteriorly, and, on the paratype, the opposing walls have grown together, but the minute aqueduct leading to the original entrance is still open. The transverse crest extends more than half way to the outer rim of the meatus and pos- terior to it, but above the deep fossa for the tractus spiralis foraminosus, is the foramen singulare. Behind the posterior angle of the internal acoustic meatus and on the posterior face of the pars cochlearis is the small cerebral orifice of the aque- duct of the cochlea. The fossa inclosing the cerebral orifice of the aqueduct of the vestibule forms the apex of a triangular area which terminates at the outer rim of the internal acoustic meatus. This area is more noticeably depressed on the para- type than on the type periotic. The cerebral and external sur- faces of the outer denser portion of the periotic are convex and the extero-ventral border of the anterior process over-rolls the external face. Measurements of Periotics (in millimeters) No. 11572, U. S. N. M. Right, Type No. 11571, U. S. N. M. Left, Paratype Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) Greatest length of periotic (tip of anterior process to tip of posterior process) Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between fenestra rotunda and tip of posterior process Distance between epitympanic orifice of aquceductus Fallopii and tip of anterior process 17.2 26.4 + 11.1 18.0 14.7-f- 14.0 Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION ^gl 15. Lamprolithax simulans''^ Kellogg, new genus and species Holotype: Right periotic, No. 11566, Division of Verte- brate Paleontology, U. S. Nat. Mus., from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Mor- rice. Coll., 1924. Paratype: No. 11568, U. S. N. M. Referred specimens, No. 11567, U. S. N. M., and Nos. 4344, 4345, 4346, Mus. Calif. Acad. Sci. Right periotic of Lamprolithax simiilans, No. 11566, U. S. N. M., X 1.0. Fig. 119. Cerebral view. Fig. 120. Inferior view. Diagnosis: Of the six periotics herewith listed, three are in the collection of the California Academy of Sciences and three in the United States National Museum. Four of these periotics are from the right side and two from the left side. Two of these six periotics have the apex of the depressed sub- triangular area behind the internal acoustic meatus produced considerably beyond the fossa inclosing the cerebral orifice of the aqueduct of the vestibule. This apex is foreshortened on the four remaining periotics. From Lamprolithax annectens the periotic of this porpoise differs in having the apex of the triangular depressed area behind the internal acoustic meatus produced beyond the fossa jvhich incloses the aqueduct of the vestibule, a smaller pars cochlearis, and a more sharply defined crest on the cerebral face of the anterior process. None of these periotics have the facet on the ventral face of the posterior process complete. This series does show that the ventral facet is traversed by ridges radiating from the raised ventro-internal margin. The posterior face of the posterior process is excavated and the external is obliquely truncated. The femainder of the periotic, viewed from the ventral side (fig. 120), resembles that of Lampolithax annectens. '2 Xa/jiTrpos, splendid; At0a^, diminutive of Xidos, a small stone, in allusion to the dense periotic hone; simtilans, imitating. 382 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Considerable variation in the contour of the internal acoustic meatus may be expected in the periotics of this porpoise, judg- ing from the differences observed in this small series. One (No. 11567, U. S. N. M.) has a very narrow meatus and another (No. 11568, U. S. N. M.) has the outer edge of the transverse bony crest separating the entrance to the aqueduct of Fallopius from the fossa for the spiral tract flush with the level of the rim of the meatus. Four, including the type peri- otic (fig. 119), have a meatus with essentially the same out- Measuremeiits of Periotics (in millimeters) No. 11566, U.S.N.M. Right, Type No. 11567, U.S.N.M. Right, Paratype No. 11568, U.S.N.M. Left, No. 4344, C. A. S. Right, No. 4345. C. A. S. Right, No. 4346, C. A. S. Left Breadth of periotic at level oi fenestra avails (from ex- ternal face above excava- tion to internal face of pars cochlearis 16.4 16.1 16.5 16.3 15.9 (') Greatest length of periotic (tip of anterior process to tip of posterior process) . . 26.3-f 26.3-f (') 25.5-1- 26.7-f (') Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most pro- jecting point on cerebral face) 9.6 9.6 9.3 10.0 8.9 Distance between fenestra rotunda and tip of an- terior process 17.2 17.4 17.8 17.3 17.0 17.8 Distance between fenestra rotunda and tip of pos- terior process 13.2-f 13.2-t- (') 14.4- 14.4- (') Distance between epitym- panic orifice of aquceduc- ductus Fallopii and tip of anterior process 13.3 13.5 14.6 13.8 13.3 13.9 ' Posterior process missing. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 333 line. The aqueduct of Fallopius and the foramen singular e . also vary in size, and on two of these periotics they show an increase of two diameters over the smallest. The vestigial original entrance to the aqueduct of Fallopius in the notch between the anterior process and the pars cochlearis is open on two of these periotics. In the others this small aqueduct has lost its connection with the functional aqueduct. On five of these periotics the transverse bony crest rises about half way to the outer rim of the internal acoustic meatus and on the sixth, as mentioned above, it is flush with the outer rim. On the last mentioned periotic, the foramen singulare is placed on the posterior face of the transverse crest about half way between the bottom of the fossa occupied by the spiral tract and the rim of the meatus. The five remaining periotics have the foramen singulare on the outer edge of the transverse crest at the same level and in approximately the same position as on the abnormal periotic. The fossa into which the aqueduct of the vestibule opens is rather large on five of these periotics and on the sixth it is nearly closed. The cerebral orifice of the aqueduct of the vestibule is situated on the posterior face of the pars cochlearis. The cerebral face rolls over upon the external face of the outer denser portion of the periotic. A small pit is present on the posterior face above the stapedial fossa. 16. Lamprolithax annectens®^ Kellogg, new species Holotype: Left periotic, No. 4343, Mus. Calif. Acad. Sci., from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Morrice, Coll., 1924. Paratype: Left peri- otic. No. 4342, Mus. Calif. Acad. Sci. Left periotic of Lamt^rolithax annecteus, No. 4343, C. A. S., X 1. Fig. 121. Cerebral view. Fig. 122. Inferior view. ' annectens, connecting. 384 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th 6er. Diagnosis: One of the two periotics referred to this species lacks most of the posterior process. The periotic of this dol- phin has a rather broad internal acoustic meatus, a deep pit on the posterior face above the stapedial fossa, a low crest on the external margin of the ventral or tympanic face of the pars cochlearis opposite to the facet for the accessory ossicle, a raised crest on the internal margin of the deep stapedial fossa which projects backward beyond the fenestra rotunda, and a flattened area between the orifice of the equceductus vestibuli and the posterior rim of the internal acoustic meatus. The margins of the facet on the ventral face of the posterior process (fig. 122) are eroded on the type periotic and the corresponding portion of the paratype periotic is lost. Ridges radiating outward from the ventro-internal margin traverse this facet. The posterior face of the posterior process is excavated above this articular surface and the external face is flattened. The ventral or tympanic face of the pars cochlearis is more or less flattened and is most strongly inflated imme- diately in front of the fenestra rotunda. The pars cochlearis swells out for a distance of 3 mm. behind the kidney-shaped fenestra rotunda, but is depressed below the crest which bounds the stapedial fossa on the inter- nal side. The fenestra ovalis does not have a complete external rim and the groove for the facial nerve does not sink below the level of the latter as it does on the periotic of Liolithax kernensis. The minute orifices of the semicircular canals are located within the vestibule in their usual position. The groove for the facial nerve leading backward from the epitympanic orifice of the aquceductiis Fallopii terminates at the postero-internal angle of the posterior process. The fossa for the stapedial muscle is deep and elongate. The narrow fossa incudis is placed on a thin projecting ledge which lies below the level of the triangular excavation on the outer denser portion of the periotic between the pos- terior process and the tuberosity. The anterior process is directed obiquely forward and in- ward, compressed from side to side, and bluntly truncated or rounded at the extremity. The cordiform articular surface for the accessory ossicle is bisected by a longitudinal elevation which follows the angle formed by the ventral and internal Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 335 faces of the anterior process. On the internal face of the tuberosity is the deep concavity for lodging the head of the malleus. The cerebral face of this periotic (fig. 121) is characterized by some well marked features. The external margin of the large internal acoustic meatus is nearly straight and the inter- nal margin is curved. Within this meatus are located the relatively large entrance to the aquceductus FaUopii and the deep fossa for the spiral tract. Some 3 mm. in front of the internal acoustic meatus is a small pit which is a remnant of a former entrance to the aqueduct of Fallopius. A broad trans- verse crest, which rises about half way to the outer rim of the meatus, separates the entrance to the aqueduct of Fallopius from the tractiis spiralis foraminosus. The small foramen singular e is situated on the outer edge of this bony partition. Behind the rim of the internal acoustic meatus is a rather large flattened triangular area having its apex formed by the fossa which surrounds the cerebral orifice of the aqueduct of the vestibule. The small aqueduct of the cochlea has its cere- Measurenients of Periotics (in millimeters) Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) Greatest length of periotic (tip of anterior process to tip of posterior process) Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between /ene^^ra rotunda and tip of posterior process Distance between epitympanic orifice of aquceductus FaUopii and tip of anterior process No. 4343, C. A. S. Left, Type No. 4342, C. A. S. Left 17.5 (•) 10.7 18.9 (•) 14.5 ' Posterior process missing. 386 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. bral orifice on the posterior face of the pars cochlearis behind the postero-internal angle of the internal acoustic meatus. The external face is considerably broader than the cerebral face of the outer denser portion of the periotic. On the cerebral face of the anterior process is a longitudinal crest. 17. Nannolithax gracilis"* Kellogg, new genus and species Holotype: Right periotic, No. 11569, Division of Vertebrate Paleontology, U. S. Nat. Mus. Diagnosis: Two periotics of this porpoise have been col- lected, one of which lacks most of the pars cochlearis, and the exact relationships of the species to those heretofore described remains to be determined. They do resemble some small peri- otics from the "molasse" of Baltringen near Biberach, in W'iirttemberg, described and figured by Probst."" Right periotic of Nannolithax gracilis, No. 11569, U. S. N. M., X 1. Fig. 123. Cerebral view. Fig. 124. Inferior view. Unlike the periotic of Grypolithax ohscurus, which bears a general resemblance to it, this diminutive ear bone is decidedly angular and the anterior process is strongly compressed from side to side distally. Some of the more important characters of this periotic are the compressed outline of the internal acoustic meatus, the attenuation of the anterior process, the relatively large size of the epitympanic orifice of the aqiicc- ductus Fall o pa, and the absence of a pit on the posterior face above the stapedial fossa. The ventral facet on the posterior process of the type peri- otic (fig. 124) is worn smooth, but fortunately that area is •* vavvos, dwarf; Ai6a^, diminutive of Xi^os, a small stone, in allusion to the dense periotic bone; gracilis, slender. "J. Probst, Ucber die Ohrenknochen fossiler Cetodonten aus der Molasse von Baltringen O. A. Laupheim. Jahreshefte d. Ver. f. vaterl. Naturk. Wiirtt., 1888, pp. 51-S2, pi. 2, figs. 12-15. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 337 fairly well preserved on the second periotic. This articular surface is subtriang^ular in outline, concave in a fore and aft direction, and its raised ventro-internal marj^in overhangs the channel for the facial nerve. The posterior face of the pos- terior process is flattened and the external is convex. The ventral surface of the pars cochlearis is convex and slopes in an antero-internal direction. The fenestra rotunda is large, circular in outline, and does not modify the posterior outline of the pars cochlearis to any appreciable extent. The external narrow rim of the fenestra oz'alis is indistinct. The deep vesti- bule is provided with the usual orifices for the small semicircu- lar canals. A low carina separates the groove for the facial nerve from the fenestra ovalis anteriorly and the stapedial fossa posteriorly. The groove for the facial nerve is rather broad and terminates at the postero-internal angle of the pos- terior process. The elongate fossa for the stapedial muscle ends anteriorly at the outer rim of the fenestra ovalis, laterally it extends downward upon the external face of the pars cochlearis and the internal face of the posterior process, and is also bounded on the internal side by a low crest. The anterior and posterior halves of the fossa incitdis meet at an obtuse angle mesially. Anteriorly this fossa occupies a narrow projecting ledge, and, posteriorly, on the antero- internal margin of the posterior process, it expands into a somewhat broader and deeper pit. In front of the abruptly truncated anterior face of the posterior process, the surface of the excavation on the outer denser portion of the periotic rises gradually to the crest of the tuberosity and is shut off inter- nally from the epitympanic recess by the raised margin of the fossa inciidis. The anterior process is attenuated, strongly compressed from side to side distally, and its ventral surface is furnished with a mesially elevated cordiform articular sur- face for the accessory ossicle of the bulla. On the internal face of the crest-like tuberosity is a rather large concavity for lodging the head of the malleus. Within the narrow internal acoustic meatus (fig. 123) is a low transverse crest which separates the compressed entrance to the aqueduct of Fallopius from the fossa occupied by the tractns spiralis forominosus. On the outer edge of the trans- verse crest and at the postero-external angle is the rather large 388 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th See. foramen singulare. The external denser portion of the peri- otic presents a two-sided, flattened cerebral surface, the inner one of which borders the internal acoustic meatus and the outer overrolls the external face. The aqueduct of the vesti- bule opens into a deep fossa and the aqueduct of the cochlea terminates below the level of the cerebral face. The external face of the anterior process is flattened and the cerebral face is rounded. Measurements of Periotics (in millimeters) Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) Greatest length of periotic (tip of anterior process to tip of posterior process) Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between /c?7e../ra rotunda and tip of posterior process Distance between epitympanic orifice of aquaductus Fallopii and tip of anterior process No. 1156Q, U. S. N. M. Right, Type U.2 23.8-h 8.8 16.8 11.7 + 12.5 No. 11570. U. S. N. M. Left (') 22.+ 16.3 10.4 + 12.8 1 Pars cochlearis damaged. 18. Platylithax robusta"'" Kellogg, new genus and species Holotype: Right periotic, No. 4339, Mus. Calif. Acad. Sci., from Sharktooth Hill, Kern County, California; Temblor Mio- cene; Charles Morrice, Coll., 1924. Diagnosis: Upon comparing this fossil periotic with those of living porpoises it was found that the periotic of Delphinus dclphis exhibits the closest approach in general size and shape. This fossil periotic is characterized by a flattened and de- '"' irXarus, broad, flat; Atflof, diminutive of \i.dos, a small stone, in allusion to the dense periotic bone; rubusla, robust. Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 339 pressed area external to the internal acoustic meatus, by having the cerebral and external faces nearly at right angles to each other, and by the swelling behind the cerebral orifice of the cochlea. The margins of the facet on the ventral face of the posterior process (fig. 126) for the corresponding process on the bulla are eroded, but it is apparent that it was originally smaller Right periotic of Flatylithax robusta, No. 4339, C. A. S., X 1.0. Fig. 125. Cerebral view. Fig. 126. Inferior view. than the corresponding facet on the periotic of Dclphinus del- phis. The ventro-internal margin of the posterior process is raised, the posterior face is flattened, and the external face is rounded. The pars cochlearis is rather large, convex, slightly inflated, and externally the surface slopes gradually to the fenestra ovalis. The fenestra rotunda is relatively small, hemi-circular in outline, and is placed on a line with the anterior margin of the stapedial fossa. The fenestra ovalis is encircled by a narrow rim which is depressed below the raised margins of the facial canal and the stapedial fossa. Within the vestibule are the usual openings of the semicircular canals. The epitympanic orifice of the aquceductus Fallopii is placed on a line with the anterior margin of the fenestra ovalis, and the canal for the facial nerve leading backward from it is par- tially concealed by the fossa incudis and the ventro-internal margin of the posterior process. The fossa for the stapedial muscle is about as wide as the fenestra rotunda and extends downward upon the external face of the pars cochlearis. The fossa incudis occupies the narrow ledge between the antero-internal angle of the posterior process and the epitym- panic orifice of the aqitceditctus Fallopii. The robust anterior process is flattened externally and rounded at the extremity. The ventral face of the anterior process is furnished with a J90 CALIFORNIA ACADEMY OF SCIENCES {Proc. 4th Ser. large articular surface for the accessory ossicle of the bulla as well as the usual concavity for lodging the head of the malleus. The excavation between the posterior process and the tuber- osity at the base of the anterior process is shut off from the epitympanic recess by the fossa incudis. Viewed from the cerebral side (fig. 125), this periotic presents a compressed internal acoustic meatus, a robust anterior process, and a flattened surface external to the acoustic meatus. The spiral tract and the foramen singulare are placed at the bottom of the internal acoustic meatus, and they are separated from the entrance to the aqucuductus Fal- lopii by a low transverse crest. The cerebral orifice of the aqiiceductus vcstihuli is compressed and is separated by an interval of 3.6 mm. from the rim of the internal acoustic meatus. Behind the minute cerebral orifice of the aqueduct of the cochlea is a sub-conical swelling. Measurements of the right periotic Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) 18.9 mm. Greatest length of periotic (tip of anterior process to tip of posterior process) 30.-f-mm. Greatest dorso-ventral depth of periotic (from most in- flated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) 12.6 mm. Distance between fenestra rotunda and tip of anterior process 20.0 mm. Distance between fenestra rotunda and tip of posterior process 15.5-|-mm. Distance between epitympanic orifice of aquccductus Fallopii and tip of anterior process , 16.3 mm. 19. Loxolithax sinuosa"" Kellogg, new genus and species Holotype: Left periotic, No. 4352. Paratype: Left periotic, No. 4351, Mus. Calif. Acad. Sci. from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Morrice, Coll., 1924. " Xo^os, slanting; \i.Oa^, diminutive of Xi^os, a small stone, in allusion to the dense periotic bone; sinuosa, sinuous. Vol. XIX] KELLOGG—PELAGIC MAMMALS OF KERN RIVER REGION 391 Diagnosis: Superficially these periotics bear a rather close resemblance to the periotic of Grypolithax pavida. They are remarkable for the angularity of their processes. The periotic of this porpoise has a broad facet on the ventral face of the posterior process, a relatively wide fossa incudis, an elongated internal acoustic meatus, a large fossa surrounding the cere- bral orifice of the aqueduct of the vestibule, and an anterior process with a laterally compressed extremity. Left periotic of Loxolithax sinuosa, No. 4352, C. A. S., X 1.0. Fig. 127. Cerebral view. Fig. 128. Inferior view. Left periotic of Loxolithax sinuosa, No. 4351, C. A. S. Cerebral view. Fig. 130. Inferior view. X 1.0. Fig. 129. Since the posterior process of the paratype periotic (fig. 130) has a much eroded ventral articular facet, the description of this structure will be based upon the type periotic (fig. 128). The ventral facet of the latter is exceptionally well preserved, the internal and posterior margins are nearly straight, but the anterior and external margins form a continuous curve. The articular surface slopes toward the diagonal depression extend- ing from the apex to the antero-internal angle. The ventro- internal margin of the posterior process is raised and con- tributes the floor for the groove which lodges the facial nerve in that region. The posterior face of the posterior process is concave and the external is convex. The pars cochlearis, viewed from the ventral side, is convex with a shallow depres- 39? CALIFORNIA ACADEMY OF SCIENCES [Pboc. 4th Ser. sion opposite the fenestra ovalis. Behind the fenestra rotunda the posterior surface of the pars cochlearis slopes to the cere- bral margin. The elHptical fenestra ovalis is completely encir- cled by a narrow rim, and the whole structure is depressed below the groove for the facial nerve. The vestibule is deep- est between the minute orifices of the semicircular canals. The fossa for the stapedial muscle is relatively deep and is bor- dered on the internal side by a sharp-edged crest. A slit-like depression is present on the posterior face above the stapedial fossa. The rather large fossa incudis occupies the thin ledge forming the lower boundary of the channel for the facial nerve in the region between the antero-internal angle of the ventral facet of the posterior process and the epitympanic orifice of the aqiiceductus Fallopii. The inner and outer margins of the fossa incudis are raised. The excavation between the posterior process and the tuberosity on the outer denser portion of the periotic is rather narrow and deep. The accessory ossicle of the bulla articulates with the anterior process on a cordiform facet, unevenly bisected by a longitudinal elevation. The distal end of the anterior process is compressed from side to side and the extremity is irregularly rounded. The tuberosity has a rounded posterior face, and the internal face bears the usual concavity for lodging the head of the malleus. Viewed from the cerebral side (figs. 127, 129), the most obvious peculiarities are the side to side compression of the anterior process, the degree of concavity of the posterior face of the posterior process, the inflation of the pars cochlearis posterior to the aqueduct of the cochlea, and the shape of the internal acoustic meatus. The internal outline of the pars cochlearis is regularly curved. On the para type periotic (fig. 129) the transverse crest separating the ejitrance to the aque- duct of Fallopius from the fossa occupied by the tr actus spiralis foraminosus attains the level of the inner rim of the internal acoustic meatus, but it is depressed below the level of the latter externally. The foramen singulare pierces the exter- nal wall of the acoustic meatus above the level of the spiral tract. The type periotic has a much lower transverse crest, and the foramen singulare is placed on the outer edge of the latter. The entrance to the aqueduct of Fallopius is large and retains its connection with the groove which marks its original Vol. XTX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 393 course, although the latter is much reduced in size. A rela- tivel)'^ broad interval separates the triangular fossa into which the aqueduct of the vestibule opens from the rim of the inter- nal acoustic meatus. The small cerebral orifice of the aque- duct of the cochlea is placed on the posterior face of the pars cochlearis behind a tuberosity which has been developed at the posterior angle of the rim of the internal acoustic meatus. Measurements of Periotics (in millimeters) Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) Greatest length of periotic (tip of anterior process to tip of posterior process) Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis, and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between fenestra rotunda and tip of posterior process Distance between epitympanic orifice of aquceductus Fallopii and tip of anterior process No. 4352, C. A. S. Left Type No. 4351 C. A. S. Left Paratype 16.3 i2S,0 !28.+ 10.5 17.8 14.9 + 14.2 20. Grypolithax obscura*^^ Kellogg, new genus and species Holotypc: Right periotic, No. 4349. Paratype: Left peri- otic, No. 4347, Mus. Calif. Acad. Sci. from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Morrice, Coll., 1924. Diagnosis: Five periotics are referred to this genus, four of which are from the left side and one from the right side. It is not improbable that future discoveries will show that two genera are included in this small series of periotics, for the ypVTTOS, curved; AtOa^, diminutive of \i0os, a small -stone, in allusion to the dense periotic bone; obscura, obscure or unknown. January 30, 1931 394 CALIFORNIA ACADEMY OF SCIE^fCES [Proc. 4th Ser. two referred to Grypolithax obscura present a quite different contour from the three referred to Grypolithax pavida. For the present and in the absence of specific information in res^ard to cranial pecuHarities, all of these periotic bones will be referred tentatively to this genus. The contours of the two periotics referred to this species are more rounded and less angular than those heretofore or hereinafter described, the pyriform internal acoustic meatus is strongly constricted anteriorly, the excavation on the outer denser portion of the periotic between the posterior process and the tuberosity is very narrow internally where it is shut off from the epitym- panic recess by the fossa incudis, and the pars cochlearis is expanded behind the level of the aqueduct of the cochlea. Right periotic of Grypolithax obscura, No. 4349, C. A. S., X 1.0. Fig. 131. Cerebral view. Fig. 132. Inferior view. The postero-external angle or apex of the posterior process (fig. 132) is missing on the type periotic. Most of the out- wardly projecting apex of this process is preserved on the paratype periotic (No. 4347. C. A. S.). In its original condi- tion the ventral facet on the posterior process was no doubt longer than wide, shallowly concave at the base, and bounded by raised ventro-internal and anterior margins. The posterior and external faces of the posterior process above this facet are convex. The ventral or tympanic face of the pars cochlearis is convex and rises rather abruptly from the fenestra ovalis. The fenestra rotunda is larger than the fenestra ovalis and produces an indentation on the posterior face of the pars cochlearis. The narrow external rim of the fenestra ovalis is complete. Within the shallow vestibule can be seen the minute orifices of the semicircular canals. The epitympanic orifice of the aqueduct of Fallopius is small, and the groove leading backward from it for the facial nerve does not sink below the level of the rim of the fenestra oz'alis and is separated from Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 395 the latter by a low carina. The fossa for the stapedial muscle is elongate and encroaches anteriorly upon the rim of the fenestra ovalis, and internally upon the outer wall of the pars cochlearis. A sharp-edged crest bounds this fossa internally. There is a depression but no pit on the posterior face above the stapedial fossa as in Grypolithax pavida. The fossa incudis is small and is bounded externally by a short carina. The posterior wall of the excavation on the outer denser portion of the periotic between the posterior pro- cess and the tuberosity rises more abruptly than the anterior wall. The anterior process is rather robust, attenuated, and roughly three-sided on the distal third, and is furnished with a nipple-like tuberosity on the extremity. The articular surface for the accessory ossicle of the bulla is elongated and rather deeply impressed. From a cerebral view the pars cochlearis (fig. 131) is seen to be not as strongly arched as in Lamprolithax simulans, the surfaces of the outer denser portion of the periotic are more rounded, the entrance to the aqueduct of Fallopius is strongly Measurements of Pcriolics (in millimeters) Breadth of periotic at level of fenestra ovalis (from external face above excavation to internal face of pars cochlearis) Greatest length of periotic (tip of anterior process to tip of posterior process) Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between fenestra rotunda and tip of posterior process Distance between epitympanic orifice of aquaductus Fallopii and tip of anterior process No. 4349, C. A. S. Right Type No. 4347, C. A. S. Left Paratype 17.2 28.7-1- 11.9 19.0 15.4-1- 15.2 396 CALIFORNIA ACADEMY OF SCIENCES [Pkoc. 4Tn Sek. compressed, and the internal face of the anterior process is creased. The internal acoustic meatus is narrowly pyriform in outline, rather deep, and incloses a reniform fossa which is occupied by the spiral tract. The transverse crest is low, rather broad, and is pierced at the postero-external angle by the small foramen singulare. The fossa which incloses the cerebral ori- fice of the aqueduct of the vestibule is narrow and rather deep. and near it in the usual position is the corresponding orifice of the aqueduct of the cochlea. The pars cochlearis swells out behind the level of these orifices. 21. Grypolithax pavida Kellogg, new species Holotype: Left periotic, No. 4348. Paratypes: No. 4350, Mus, Calif. Acad. Sci., and No. 11575, Division of Vertebrate Paleontology, U. S. Nat. Mus., from Sharktooth Hill, Kern County, California; Temblor Miocene; Charles Morricc, Coll., 1924. Left periotic of Grypolithax pavida, No. 4348, C. A. S., X 1.0. Fig. 133. Cerebral view. Fig. 134. Inferior view. ' Diagnosis: On direct comparison, the periotics of this por- poise as a rule are separable from those of Grypolithax obscura by the presence of an irregularly flattened area on the cerebral face of the outer denser portion of the periotic, a broader excavation between the posterior process and the tuberosity, a low crest on the antero-external border of the ventral face of the pars cochlearis, and a more rounded extremity of the anterior process. It seems unnecessary to give a detailed description of the periotic of this porpoise inasmuch as most of it would be merely a repetition of the preceding description. Attention is directed to the presence of a slit-like pit on the posterior face above the stapedial fossa on two of these periotics (Nos. 4348, Vol. XIX] KELLOGG— PELAGIC MAMMALS OF KERN RIVER REGION 397 4350, C. A. S.), but on the third (No. 11575, U. S. N. M.) it is barely discernible. The posterior and external faces of the posterior process immediately above the ventral facet are shelving. The inflation of the pars cochlearis posteriorly is accentuated by a short crease which commences at the inner angle of the crescentic fenestra rotunda and proceeds inward in the general direction of the aqueduct of the cochlea. The articular surface (fig. 134) for the accessory ossicle of the bulla is subcordiform in outline, with a medial longitudinal elevation. Opposite this facet and on the ventral face of the pars cochlearis is a low crest which is quite distinct on two of these periotics (Nos. 4348, C. A. S., and 11575, U. S. N. M.), but is rather indistinct on the third (No. 4350, C. A. S.). On the type periotic (fig. 133), the closure of the opposing walls of the original entrance to the aqueduct of Fallopius has been completed, leaving a minute orifice on the anterior margin of the pars cochlearis. The two remaining periotics illustrate the manner in which this closure has been accomplished. Measurements of Periotics (in millimeters) Breadth of periotic at level of fenestra ovalis (from external face above excavation to inter- nal face of pars cochlearis) Greatest length of periotic (tip of anterior pro- cess to tip of posterior process) . . 7 Greatest dorso-ventral depth of periotic (from most inflated portion of tympanic face of pars cochlearis and external excavation to most projecting point on cerebral face) Distance between fenestra rotunda and tip of anterior process Distance between fenestra rotunda and tip of posterior process Distance between epitympanic orifice of aqucB- ductus Fallopii and tip of anterior process. . . No. 4348, C. A. S. Left Type No. 4350, C. A. S. Left Paratype 16.2 16.4 26.9 26.5 9.7 9.9 17.9 16.9 13.9 + 14.6 + 14.5 13.7 No. 11575 U. S. N. M. Left Paratype 16.5 26.6 10.4 17.3 13.9 + 13.1 PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES Fourth Series Vol. XIX, No. 13, pp. 399-410 May 29, 1931 XIII REPORT OF THE PRESIDENT OF THE ACADEMY FOR THE YEAR 1930 BY C. E. GRUNSKY President of the A cademy Following the usual practice, attention will first be directed in this report to the Academy's membership. There has been but little change in the total, despite the fact that a special effort brought in about 150 new members. The members are classified as follows : Patrons 19 Honorary Members 15 Life Members 94 Fellows 63 Members 923 Junior Members 10 Total ^ 1124 Of these: 7 Life Members are also Fellows 7 4 Patrons are also Life Members 4 1 Fellow is also an Honorary Member 1 3 Fellows are also Patrons 3 1 Patron is not a member 1 Total 16 Actual Membership 1 108 May 29, 1931 400 CALIFORNIA ACADEMY OF SCIENCES [Pnoc. 4th Ser. On January 1, 1930, the number of members stood at 1086 New Membeis were added during the year 150 Members lost by death 27 Members resigned 43 Members dropped (non-payment of dues) 58 128 Net gain during year 22 Leaving the membership on January 1, 1931, at 1108 The Academy carries on its list of benefactors the following names : Mr. James Lick Deceased Mr. Ignatz Steinhart The Academy carries on its list of patrons the following names : Mr. George C. Beckley Dr. Frank E. Blaisdell Mr. William B. Bourn Hon. William H. Crocker Mr. Peter F. Dunne Miss Alice Eastwood Dr. Barton Warren Evermann Mr. Herbert Fleishhacker Hon. Joseph D. Grant Mr. Edward Hohfeld Living Mrs. Albert Koebele Mr. A. Kingsley Macomber Mr. John W. MaiUiard Mr. Joseph MaiUiard Mr. M. Hall McAllister Mr. G. Frean Morcom Mr. William C. Van Antwerp Mr. Edward P. Van Duzee Dr. E. C. Van Dyke Mr. William Alvord Mr. Charles Crocker Mr. W. M. Giffard Mr. John W. Hendrie Mr. William F. Herrin Mr. Henry M. Holbrook Deceased Mrs. Charlotte Hosmer Mr. Ogden Mills Mr. Alexander F. Morrison Mr. Amariah Pierce Dr. John Van Denburgh Vol. XIX] GRUNSKY— PRESIDENT'S REPORT FOR 1930 401 Academy members who were called by death in 1930 are as follows : Dr. Thomas Addison Member April 5 Mr. Harry Babcock Member February 24 Mr. Robert C. Bolton Member August 25 Mr. Elisha Brooks Life Member May 1 1 Mr. James F. Campbell Member Janviary 3 Mr. Warren D. Clark Member May 9 Prof. John N. Cobb Member January 13 Dr. Lawrence A. Draper Member January 3 Mr. A. L. Duncan Member August 19 Col. George C. Edwards Life Member November 19 Mr. A. W. Foster Member October 14 Mr. Wm. J. Gilliland Member November 30 Mr. William Herrmann Member September 30 Mr. Leonard Howarth Member May 12 Mr. W. B. Lewis Member August 26 Mr. A. S. Mangrum Member September 3 Mr. Stephen T. Mather Member January 22 Dr. William D. Matthew. . . .Member September 24 Mr. Robert S. Moore Member February 16 Mr. John Partridge Member August 14 Capt. Albert H. Payson Member January 25 Hon. James D. Phelan Life Member. August 7 Mr. G. P. Rixford Life Member October 27 Mr. J. H. Skinner Member June 12 Mr. William H. Talbot Member November 5 Mr. John L Walter Member March 5 Dr. Lucy M. F. Wanzer Life Member October 20 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1929 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 1930 In the year 1930, eleven free lectures were delivered at the stated meetings of the Academy, as follows: January 2. "The Horsetown Formation of California." By Mr. Frank M. Anderson, Honorary Curator, Department of Paleontology, California Academy of Sciences. March 5. "A Sub-arctic Summer." Illustrated. By Mr. Harry S. Swarth, Curator, Department of Ornithology and Mammalogy, California Academy of Sciences. April 2. "A Visit to the Desert and Forests of Australia." Illus- trated with motion pictures. By Mr. Joseph R. Slevin, Curator, Department of Herpetolog}^ California Acad- emy of Sciences. 402 May 7. CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. June 4. July 2. August 6. September 3. October 1. November 5. December 3. "A Panamanian Pasear." Illustrated. By Mrs. M. E. McLellan Davidson, Assistant Curator, Department of Ornithology and Mammalogy, California Academy of Sciences. "Bird Banding." By Mr. Joseph Mailliard, Curator Emeri- tus, Department of Ornithology and Mammalogy, Cali- fornia Academy of Sciences. "Flags." Illustrated. By Mr. C. B. Lastreto, San Francisco. "The Proposed Salt Water Barrier in the Upper Bay Waters." By Dr. C. E. Grunsky, President, Cali- fornia Academy of Sciences. "Floral Zones of the California Deserts." Illustrated. By Mr. John Thomas Howell, Assistant, Department of Botany, California Academy of Sciences. "Seventh International Ornithological Congress, Amster- dam." B}^ Mr. Harry S. Swarth, Curator, Department of Ornithology and Mammalogy, California Academy of Sciences. "Our South Sea Islands." Illustrated b}' motion pictures and stereopticon slides. By Mr. Alvin Scale, Superin- tendent of the Steinhart Aquarium of the California Academy of Sciences. "A Report on My Trip to the International Botanical Con- gress." Illustrated. By Miss Alice Eastwood, Curator, Department of Botany, California Academy of Sciences. The Sunday afternoon lectures at the Museum building were continued throughout the year except during the vaca- tion months of summer. Despite the inadequacy of the tem- porary lecture room, the attendance at these lectures has been satisfactory. These lectures have included the following: January 5. "With a Moving Picture Camera in Africa." Illustrated. By Dr. E. C. Franklin, Professor of Organic Chemistry, Stanford University. January 12. "East Winds." By Mr. E. A. Beals, Consulting Meteor- ologist, Alameda, California. January 19. "Aviation and Meteorology." Illustrated. By Mr. D. R. Reed, Assistant Forecaster, United States Weather Bureau, San Francisco. Vol. XIX] GRUNSKY— PRESIDENT'S REPORT FOR 1930 403 January 26. "The Climate of the Pacific Northwest." By Mr. Melvin B. Summers, in charge of the Seattle Weather Bureau and Climatological Service of the State of Washington. At present with the San Francisco office. February 2. "Indians of Yosemite and Their Legends." Illustrated. By Mr. Ansel F. Hall, Chief Naturalist, National Park Service. February 9. "Geolog>' of the Lassen Region." Illustrated. By Mr. Harold Stein, Field Executive, Boy Scouts of America, San Francisco. February 16. February 23. "Personal Experiences with Black and Grizzly Bears." Illus- trated. By Mr. Joseph Dixon, Economic Mammalo- gist, Univeristy of California, Berkeley. "Prehistoric Peoples of the Southwest." Illustrated. By Mr. Ansel F. Hall, Chief Naturalist, National Park Service. March 2. March 9. "An Engineer's Trip to Japan and Adjacent Countries." By Dr. C. E. Grunsky, President of the California Academy of Sciences. "Desert Insects." Illustrated. By Dr. E. C. Van Dyke, Curator Emeritus, Department of Entomology, Cali- fornia Academy of Sciences. March 16. "Some Problems in Game Conservation." Illustrated with motion pictures. By Dr. H. C. Bryant, Director, Bureau of Education, California Division of Fish and Game. March 23. "The Amphibians of California." Illustrated. By Dr. Tracy I. Storer, Associate Professor of Zoology, Uni- versity of CaHfomia, College of Agriculture, Davis, California. March 30. "Game Trails; Steelhead Fishing on the Klamath." Illus- trated. By Mr. Paul Fair, in Charge of Exhibits, United States Forest Service, San Francisco. April 6. "Tumors." By Dr. William Ophuls, Dean of the School of Medicine and Professor of Pathology, Stanford Uni- versity School of Medicine. April 13. "Recent Advances in Public Health." By Dr. Herbert F. True, Assistant Health Officer, City and County of San Francisco. 404 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. April 20. April 27. May 4. May U. May 18. October 5. October 12. October 19. October 26. November 2. November 9. November 16. November 23. "Trichinosis and Its Prevention." By Dr. Karl F. Meyer, Director of the Hooper Foundation, University of Cali- fornia Medical School. "The High Cost of Quackery." By Dr. E. L. Gilcreest, Instructor in Surgery, University of California Medical School. "General Aspects of Tuberculosis." By Dr. Robert A. Peers, Member of the California Department of Public Health. "Pain." By Dr. John Homer Woolsey, Assistant CHnical Professor of Surgery, University of California Medical School. "The Cost of Being Sick." By Dr. Morton R. Gibbons, Lecturer on Medical Aspects of Insurance, University of California Medical School. "Fur Seals: A Million Dollar Business." Illustrated. By Dr. George Haley, Professor of Biology, St. Ignatius College, San Francisco. "Control of Predatory Mammals." Illustrated. By Dr. E. Raymond Hall, Curator of Mammals, California Museum of Vertebrate Zoology, University of Cali- fornia. "George Washington's First Wish." By Mr. Edward Ber- wick, Pacific Grove, California. "The Way Wild Animals Do Things." Illustrated. By Dr. W. E. Ritter, Professor of Zoology, Emeritus, Scripps Institution of Oceanography, La Jolla, California. "Cahfornia Floral Zones." Illustrated. By Mr. John Thomas Howell, Assistant, Department of Botany, California Academy of Sciences. "Game Birds of Cahfornia." Illustrated. By Mr. Donald McLean, Field Naturalist, Cahfornia Fish and Game Commission. "African Big Game." Illustrated. By Mr. N. B. Liver- more. Member Board of Trustees, California Academy of Sciences, San Francisco. "Our National Parks." Illustrated. By Colonel John R. White, Superintendent, Sequoia National Park, Cali- fornia. \'0L. XIX] GRUNSKY— PRESIDENT'S REPORT FOR 1930 405 November 30. December 7. December 14. December 21. December 2S. "Reptiles and Amphibians, with especial Reference to the Rattlesnakes of California." Illustrated with motion pictures and stereopticon slides. By Mr. Joseph R. Slevin, Curator, Department of Herpetolog>', Cali- fornia Academy of Sciences. "A New Conception of Health Insurance as it vitally con- cerns the general public." Illustrated. By Dr. Ralph A. Reynolds, San Francisco. "The Mountains and Canyons of the Sequoia National Park." Illustrated. By Mr. Francis P. Farquhar, Secretary Commonwealth Club, San Francisco. "The Animal Kingdom: The Reservoir of Disease." Illus- trated. By Dr. Karl F. Meyer, Director of the Hooper Foundation, University of California Medical School. "The Natural History of Magpies." Illustrated. By Dr. J. M. Linsdale, Research Associate in the Museum of Vertebrate Zoology, University of California. Li.ST OF Academy Publications in 1930 Proceedings, Fourth Series Vol. XVIII, Nos. 17 and 18, pp. 531-586. No. 17^Report of the President OF the Academy for the Year 1929, by C. E. Grunsky. No. 18 — Report OF the Director of the Museum and of the Aquarium for the Year 1929, by Barton Warren Evermann. (Issued April 8, 1930.) Vol. XIX, Nos. 1, 2 and 3, pp. 1-22. No. 1, pp. 1-6 — Marine Mollusca of Guadalupe Island, Mexico, by A. M. Strong and G. D. Hanna. No. 2, pp. 7-12 — M.\RINE MOLLUSKA OF THE ReVILLAGIGEDO ISLANDS, MEXICO, by A. M. Strong and G. D. Hanna. No. 3, pp. 13-22 — Marine Mollusca OF THE Tres Marias Islands, Mexico, by A. M. Strong and G. D. Hanna. (Issued June 4, 1930.) ■• Vol. XIX, Nos. 4 and 5, pp. 23-56, plates 1-3, 4 text figs. No. 4, pp. 23-40, plate 1, 4 text figures — Some Rissoid Mollusca from the Gulf of Cali- fornia, by Fred Baker, G. D. Hanna and A. M. Strong. No. 5, pp. 41-56, plates 2-3 — Some Mollusca of the Family Epitoniidae from the Gulf of California, by Fred Baker, G. D. Hanna and A. M. Strong. (Issued July 15, 1930.) Vol. XIX, No. 6, pp. 57-64 — Pliocene Deposits North of Simi V.vllev, C.\LiFORNiA, by W. P. Woodring. (Issued July 15, 1930.) Vol. XIX, No. 7, pp. 65-83, 3 text figs. — Geology of Sharktooth Hill, Kern County, C.\lifornia, by G. Dallas Hanna. (Issued July 15, 1930.) 405 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Vol. XIX, No. 8, pp. 85-93, 7 text figures — Fossil Bird Remains from the Temblor Formation Near Bakersfield, California, by Alexander Wetmore. (Issued July 15, 1930.) Vol. XIX, No. 9, pp. 95-104, 1 text figure — The Killifish of San Ignacio AND the Stickleb.vck OF San Ramon, Lower C/Vlifornia, by George Sprague Myers. (Issued July 15, 1930.) Vol. XIX, No. 10, pp. 105-108 — Contributions to Oriental Herpetology IV. Hokushu or Yezo, by Joseph R. Slevin. (Issued July 15, 1930.) Vol. XIX, No. 11, pp. 109-215, plates 4-15^Marine Algae of the Revilla- GiGEDO Islands Expedition in 1925, by William Albert Setchell and Nathaniel Lyon Gardner. (Issued December 30, 1930.) Handbook of the Birds of Golden Gate Park, San Francisco, by Joseph Mailliard. Items of Interest Some notable changes have occurred in the personnel of the Officers of the Academy. Mr. M. Hall McAllister resigned as Treasurer on July 1, 1930. In accepting his resignation, the Board of Trustees passed the following resolution : "In accepting the resignation of Mr. M. Hall McAllister as a Trustee of the California Academy of Sciences, the Board does so with very great regret and feelings of real loss. During Mr. McAllis- ter's many years of service as a member of the Board, he was ever watchful of the best interests of the Academy. His services as Trustee and Treasurer were of the greatest help to the institu- tion and the Board wishes to express its high appreciation of his deep interest in the welfare of the Academy." Mr. F. W. Bradley was appointed to fill the unexpired term. It is also to be noted that after long and faithful service beginning January 6, 1902, ]\Ir. J. W. Hobson retired at his own request from the office of Recording Secretary. His services in this capacity terminated on February 19, 1930. It was with sincere res:ret that his associates on the Council saw his relinquishment, owing to physical disability, of the duties he had so long performed. His place has been filled by Mrs. J. W. Hobson. who had for some time been assisting Mr. Hobson in the keeping of records and other work connected with the office. Vol. XIX] GRUNSKY— PRESIDENT'S REPORT FOR 1930 49/ On October 27, 1930, the Academy lost, by death, Gulian Pickering Rixford, for many years a member of the Academy, one time its Recording Secretary, and at the time of his death. Librarian since December 24, 1924. The vacancy caused by Mr. Rixford's death was filled by his son, Dr. Emmet Rixford. On November 19, the Academy lost, by death. Colonel George Cunningham Edwards, also for many years a member and First Vice-President since January 21, 1907. Second Vice-President, Otto von Geldern, was appointed to fill the vacancy in the office of First Vice-President, and Dr. Wm. E. Ritter was appointed Second Vice-President. Donations to the publication fund to be used in the publica- tion of a handbook on the Birds of Golden Gate Park, by Joseph Mailliard, have been made during the year as follows : Mrs. F. W. Bradley (Mary Parks Bradley) $200 Mr. Selah Chamberlain 200 Mr. William H. Crocker 200 Mr. Herbert Fleishhacker 200 Mr. J. D. Grant 200 Mr. Chas. Kendrick 200 Mr. Edward J. McCutcheon 250 • Mr. Louis F. Monteagle 200 A donation of $1,200 to the Department of Botany was made by Miss Alice Eastwood, Curator of that Department. By reason of this donation. Miss Eastwood became a Patron of the Academy. Mr. McAllister has again contributed the sum of $100 to the Committee on the Conservation of Wild Life, of which he is Chairman. For some years past he has made a like annual contribution. The Academy, some time ago, expressed its willingness to cooperate with the Seismological Society of America and has now allotted definite space in the basement of the museum building for the installation of a seismograph. When this is installed the Academy will provide the necessary observer. The installation is being made without cost to the Academy. Several months ago a representative of Karl Zeiss and Company was in San Francisco to awaken interest in the erec- tion of a Planetarium. The apparatus for a planetarium such 40g CALIFORNIA ACADEMY OF SCIENCES [Proc. 4tii Ser. as the Adler Zeiss Planetarium of Chicaij^o. the Veh Zeiss Planetarium of Philadelphia and the Griffith Zeiss Plane- tarium of Los Anc^eles, the latter about to be erected, is manu- factured and furnished by the Zeiss Company. While no progress appears to have been made in enlisting financial sup- port for this project, opportunity was nevertheless afforded to the Academy to express its interest in the matter and to offer to accept the management of the planetarium if the same be located on some site convenient to the buildings of the Acade- my in Golden Gate Park. The popularity of the Steinhart Aquarium has not waned. On Saturdays, Sundays, and holidays, the Aquarium is fre- quently over-crowded. More floor space is needed for the convenience of visitors and much more tank space is needed for additional material. The aquarium at San Francisco should be second to no other aquarium in this country. Ap- preciating this fact, an appeal was made to the city authorities several months ago for funds, in the amount of $750,000, for an extension to the aquarium. This sum would suffice to treble the floor and tank space. It would be a gracious act on the part of the City either out of current funds or by means of a bond issue to provide the money now needed for the en- largement of the Steinhart Acjuarium. It is hoped that this view will prevail. The Academy is about to begin the erection of the first unit of an East Wing in which the Leslie Simson African Mammal collection is to be installed. Material for the exhibits sent from Africa by Mr. Simson is arriving from time to time. Our Curator of Exhibits, Mr. Tose, has recently returned from Africa where he collected material for accessories and made color sketches of the habitats of the wild life which is to be put on display. But here, as in the case of so many of the Academy's activities, not all can be done which should be done. There is a sore lack of funds with which to erect ade- quate buildings. In the circumstances the Academy has felt impelled to have recourse to its credit and has borrowed some $255,000 with which to begin the erection of its East ^^ ing. While this entails a large annual outgo for interest, yet it appears fully justified in view of the fact that Mr. Simson has him.self turned over to the Academy, or rather has placed Vol. XIX] GRUNSKV—PRESIDEXT'S REPORT FOR 1930 409 in escrow, property having an aggregate value of about $150,000, which will offset in some measure the Academy's proximate outlay of capital. While this sum stands as the property of the Academy, the income therefrom must go to Mr. Simson during his lifetime. In its present quarters the Academy has insufficient space. The collections are expanding in its various departments and even passageways are being over-stocked with cases of re- search material. In view of this fact and because of the urgent need of extending research activities, the officers of the Academy made an appeal to the Rockefeller Foundation for funds with which to erect all of the proposed East Wing except only the Auditorium. This application has quite re- cently been denied. Building activities will, therefore, have to be restricted to the first unit, for a time at least, until some one comes to the Academy's aid with an adequate endowment or bequest. Plans for the East Wing of the Academy have been pre- pared by Architect Lewis P. Hobart. These had been suf- ficiently advanced a few weeks ago to permit calling for bids to construct the first unit thereof, which is urgently needed both for the housing of the African mammal exhibits as ex- plained, and for the expansion of the Academy's research activities. Satisfactory proposals having now been received, it is ex- pected that before the end of this year the building will be available for occupancy. In this connection a word relating to the finances of the Academy will not be out of place. The book value of the ^assets of the Academy appears at $2,143,629. At the time of the completion of the West Wing of its buildings in Golden Gate Park in 1916, the Academy was in debt about $350,000. This indebtedness was gradually reduced to $195,000 at which amount it stood when the new loan was made a short time ago for present building purposes, which, in the course of the current year, will bring the total indebtedness to $450,000. But as already explained, the in- creased indebtedness is in part offset by the property received from Mr. Simson and now in escrow for the Academv. 410 CALIFORNIA ACADEMY OF SCIENCES [Pnoc. 4th Ser. The valuable work being clone in the Academy's depart- ments will appear from the several reports of the Director of the Museum, of the Curators of the various departments, and of the Superintendent of the Aquarium. To all of those who have in any way contributed to the Academy's activities, I desire on behalf of our membership for whom I am speaking, to express sincere appreciation. This extends, too, to the services of Attorney Edward Hohfeld who has ever been ready to assist with advice when called upon. In looking back over the year's activities, some progress is to be noted, but the Academy is still waiting and hoping for an endowment of sufficient magnitude to place it where it belongs, — well up in the front rank of like institutions else- where in the world. PROCEEDINGS OF THE CALIFORNIA ACADEMY OF SCIENCES Fourth Series Vol. XIX, No. 14, pp. 41 1-482 May 29, 1931 XIV REPORT OF THE DIRECTOR OF THE MUSEUM AND OF THE AQUARIUM FOR THE YEAR 1930 BY BARTON WARREN EVERMANN Director of the Museum and of the A quarium The Annual Report of the Director for the year 1929 was presented to the Academy at the Annual Meeting, February 19, 1930. The present report, submitted at this Annual Meet- ing, February 19, 1931, sets forth briefly the scientific and educational activities of the Academy for the calendar year 1930. Personnel The employees of the Museum as of January 1, 1931, were as follows : Dr. Barton Warren Evermann, Director and Executive Curator of the Museum and of the Aquarium, and Editor of the Academy publications ; Susie M. Peers, Secre- tary to the Board of Trustees; Annie G. Hobson, Recording Secretary of the Academy; Alice Eastwood, Curator. John Thomas Howell, Assistant Curator, and Kate E. Phelps, as- sistant. Department of Botany ; Edward P. Van Duzee, Cura- tor, J. O. Martin and Amy Williamson, assistants, Dr. Edwin C. Van Dyke, Honorary Curator, Dr. Frank E. Blaisdell, Re- search Associate, and Dr. Frank R. Cole, Associate Curator 412 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. in Dipterology, Department of Entomology ; Frank Tose, Chief, and Richard Cayzer and Cecil Tose, assistants, Depart- ment of Exhibits ; Dr. Barton Warren Evermann, Curator, and H. Walton Clark, Assistant Curator, Department of Fishes ; Joseph R. Slevin, Curator, Department of Herpetology ; Dr. Walter Kenrick Fisher, Curator, Department of Inver- tebrate Zoology ; Thomas Cowles, Assistant Librarian, and Veronica J. Sexton, Library assistant; Harry S. Swarth, Cura- tor, Mary E. McLellan Davidson, Assistant Curator, and Joseph Mailliard, Curator Emeritus, Department of Orni- thology and Mammalogy ; Dr. (j. Dallas Hanna, Curator, Dr. Leo George Hertlein, Assistant Curator, Winifred Morrison, and John L. Nicholson, Jr., assistants. Dr. Frank M. Anderson, Honorary Curator, and Dr. Roy E. Dickerson, Research As- sociate, Department of Paleontology ; Constance W. Camp- bell, stenographer, part time ; Evelyn Larsen. office assistant, part time : Raymond L. Smith, general assistant ; Mabel E. Phillips, check-room attendant; William C. Lewis, janitor; Hugh Jones, assistant janitor; Allen Weatherwax, lecture at- tendant; Patrick O'Brien, day watch; Archie McCarte, night watch; Nellie Marshall, attendant, part time; Fred Tanaka, janitor, part time. The Aquarium staff and employees as of January 1, 1931, were as follows : Dr. Barton Warren Evermann, Director ; Susie M. Peers, Secretary, part time ; Constance W. Campbell, stenographer, part time ; Evelyn Larsen. office assistant, part time ; Alvin Scale. Superintendent ; Robert J. Lanier. Assis- tant Superintendent ; Phyllis Beardslee. doorkeeper ; Clynt S. Martin, chief engineer; B. T. Culleton, first assistant engi- neer ; John A. Dwyer, second assistant engineer ; Clyde E. Guidry, chief attendant; Jack Solini, first assistant attendant; L. R. Solini, second assistant attendant ; Leon Maxwell, third assistant attendant; Frank J. Maxwell, relief engineer and at- tendant ; S. J. Shenefield, carpenter and general utility man ; Patrick O'Neill, janitor; Patrick McArdle, assistant janitor; Frank Haley, day watch. May Peffer, library assistant, resigned January 11, 1930. Her place was taken by Veronica J. Sexton, February 7. Barbara Cowles was employed as temporary library assistant from December 8, 1930, to January 1, 1931. Robert Thfinip- Vol. XIX] EVERMAXS— DIRECTOR'S REPORT FOR 1930 4^3 son. Jr.. lecture attendant and library assistant, resigned June 10. 1930. Allen W'eatherwax took his place as lecture atten- dant October 5, 1930. Russell Hendrick, assistant, Depart- ment of Exhibits, resigned May 16, 1930. Winifred Mor- rison began work as assistant in the Department of Paleon- tology. March 12, 1930. James Campbell was employed as tem- porary assistant in the Department of Fishes part time in 1930. Harold Thayer was employed as temporary assistant in the Department of Fishes from April 26 to June 12, 1930. Mrs. Nellie Marshall began work as part time attendant February 9. 1930. Enid A. Larson began work June 16 as temporary check-room attendant in the absence of Mabel Eleanor Phillips. She was employed in this position up to October 15. She worked in the Department of Fishes from October 15 to November 15, and in the Department of Herpe- tology from December 1 to 6, 1930. Gust Anderson was em- ployed as temporary night watchman in the absence of Hugh R. Jones from September 1 to 20, 1930. J. N. Angelucci, third assistant attendant, resigned August 31, 1930. Leon Maxwell took his place September 1, 1930. Peter Busalacchi was employed as temporary help, November 12, 1930. in place of Leon Maxwell who was injured and temporarily unable to work. Robert J. Lanier was appointed Assistant Superinten- dent of the Steinhart Aquarium February 1. 1930. Charles W. Hibbard, assistant collector, resigned November 16, 1930. Elsie von Larisch was employed as temporary typist from August 4 to October 31. Frank Haley took the place of James Cavanaugh as day watch. Cooperation with Publjc and Private Schools, with Other Institutions, and with Individuals The Museum continues to be of service to the schools, other institutions, and individuals in their educational and scientific work. All available space for public exhibits has long since been utilized ; nevertheless, our Department of Exhibits continues, as material and time permit, to prepare new educational ex- hibits to put on display so soon as suitable exhibition rooms become available. 414 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. During the year the research collections in the various de- partments increased greatly, particularly in the departments of Botany, Entomology and Paleontology, as is shown in the reports of the respective curators. Twelve portable habitat groups of animals were loaned to the Berkeley public schools where they were kept in circulation throughout the school year. At the end of the school year these portable exhibits are returned to the Academy for in- spection and storing during the summer vacation. The Academy continues to loan to schools and investigators speci- mens of birds, mammals and other objects requested. And quite a number of investigators and special students come to our laboratories, particularly in botany, ornitholog}^ herpe- tology and paleontology, for the purpose of special study. The Academy receives many letters from the general public, asking for information on many and diverse subjects, not all of a scientific nature. These are usually referred to the appropriate department and the information requested is supplied, whenever possible, by the Director or the Curator of the department concerned. This frequently requires a considerable amount of time in re- search or consultation of literature. /OL. XIX] £F£ RM/ INl ON fo 1^ ON CN ^— ( ■* NO i-H T— ( ON t^ Oi On lo ii-H o i-H o t-- ^ NO ON *— ( o S t^ •* On_^ CN On_ o NO ■* NO O 00 CO CO O t-^T o OO CN On CO cn" t^ o" o r^ T-H CO >-^ rn rn '^ CO •* ■ri< NO NO CO CO CO CN ON ^ o_ t~~ O. o On 00 00 00 o m o ID t^ NO NO "^ vO OO ^— » *-H ON m 00 y~i CN -* CO On 1^ c^ t^ t^ NO "* CO On_ NO 00 o^ T-H lO 00 On_ Tf 0\ vO On o* ^— 1 "1 00 CN """ o '^ On in o *-i P^ fN '^ CO 5^ NO NO NO m CO CO c^ CN ID OS o ^ "-> On o NO CN rq ^ m t^ r-1 lO o nO CN o o OO 00 On 00 T— 1 O oo 00 vO_ "*. 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J2 O 'rt ■tj o E- Vol. XIX] EVERMANN— DIRECTOR'S REPORT FOR 1930 417 Schools Visiting the Museum in 1930 Following is a list of the schools, the grades, teachers, num- ber of pupils, and dates of visits in 1930 : San Francisco Schools Visiting the Museum in 1930 Date 1930 Jan. 25 " 31 " 31 4 Grade Feb. 6 6 6 7 7 8 " 13 " 14 " 14 " 17 " 18 " 18 " 25 " 26 " 26 " 28 " 28 Mar. 5 6 6 " 16 " 10 " II " U " 11 " 14 " 14 " 14 " 15 " 19 " 20 " 20 " 21 " 22 " 23 " 23 " 25 " 25 " 26 " 26 " 27 " 27 " 27 " 28 " 31 " 31 38 36 27 66 43 74 3i 46 27 34 19 40 33 28 35 33 32 72 25 40 32 School Everett Jr H9. . . Commodore Sloat 5th . . . Hawthorne 6B . . . Sherman 6B .... Sherman 2-3B . . Le Conte 4A-4B Sarah B. Cooper 3A-3B Sherman SB . . . John Muir Ungraded 14 Everett Jr. High G9-H9 15 Hawthorne 6H .... Golden Gate 4A . . . . Columbus 6B .... Poly. H. S L2-Biol Jean Parker 4A .... Patrick Henry 5A Le Conte 3B . . . . Hawthorne 5A-5B . Commodore Stockton 5 A E. R. Taylor 3B . . . . Jean Parker 5B-6A . E. R. Taylor 3B Grant 4B . . . . Columbus 3A-B . . Everett Jr. High Junior H 16 Crocker Jr. High H9 30 Argonne 6A 34 Poly. H. School 10 18 Francis Scott Key 4A 38 Sarah B. Cooper Ungraded 14 Guadalupe 5A 38 Adams 3A-2B 24 State Teacher's College 17 Outdoor School .^. Kindergarten .... 15 Franklin Jr. Primary 22 Galileo High School 17 Bret Harte Ungraded 11 Everett Jr. High H9 10 ... 46 ... 24 ... 31 ... 10 ... 30 ... 100 ... 58 ... 36 ... 37 ... 36 ... 33 ... 40 Portola l-7th .... Commodore Stockton 4A Sheridan 4A Lincoln Ungraded . Monroe 5 A Presentation 8B-7B ... Com. Stockton 4A-4B ... Burnett 3 A Sunnyside 5 A Argonne 2A Lafayette 7th-8th . . . Junipero Serra 5 A Number Pupils Teacher 15 E. Browne M. d'E'-lach F. C. Muller M. Doran C. R. Murray, A. Turner Jeannie Strassner C. MacCurra.T. Meachum M. Denny M. L. Kennedy Elsie Browne C. Hackman, M. Gallagher M. Maughan Isabel Elkins J. Koehler C. Seidker E. MacLean Miss Michel M. E. Doherty H. F. Jamieson K. M. Brazell M. Valsangiacomo O. Wilcox E. Johnson M. K. Schnittger E. Browne M. Hibbard J. A. Plevin Koehler O. Schell R. Stauer M. Johnson A. McVeigh Lea Reid Marie Brown Marie A. Reilly E. Kluegel C. W. Sullivan E. Browne M. Crosby H. Jacobs M. A. Lentz F. A. Brierly N. P. Hockley S. Xaveria M. Richter, M. Holl A. Gibson F. Kelly F. Stockton M. Copeland Miss Akers 418 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. San Francisco Schools Visiting the Museum in 1950— Continued Date 1930 April 2 2 3 " 3 " 4 " 4 " 5 " 5 " 5 8 " 8 9 9 " 10 " 10 " 11 " 11 " 17 " 18 " 19 " 21 " 23 " 23 " 23 " 28 " 29 •' 29 May 8 9 9 " 13 " 13 " 13 " 13 " 13 " 14 " 14 " 14 " IS " IS " 16 " 16 " 16 " 19 " 21 ' 21 ' 21 ' 21 ' 22 ' 22 ' 22 ' 23 ' 23 ' 23 " 23 " 26 " 26 34 35 37 76 School Grade Twin Peaks lA-lB Bernal 7B Bernal 7A Paul Revere SA Washington Irving 5B-6A Sherman Ungraded 11 Jefierson Union 8th 12 Prescott 6th 34 Everett Jr. High Mixed 14 Fremont High 6th 37 Galileo High School 20 Poly. High School H9 13 Dudley Stone Special 33 Guadalupe 6-7-8-Girls 43 Bryant 4-5 27 E. R. Taylor 4B Grade 26 Marshall 3A 28 Knightsen 2-3-4-5 30 Daniel Webster Tumbling CI 17 Everett Jr. High Mixed 12 Emerson 2A 25 Jean Parker Sight Con 12 Hamlin School 3 12 Number Pupils Teacher . 21 Florence McNeill Olive A. Perry B. Kelly M. J. Ludwig Edna Murphy C. Middleton M. Miller M. Campanari W. Browne S. A. Perry Miss Kautz Koehler G. Mosby, M. Jones K. Growney L. Moncrieff E. M. Roth M. Mack A. Frey, E. Moody D. Husing E. Browne M. H. Leibel U. Duane Sunnyside 6B . . . . Burnett 4A . . . . St. Agnes Second. St. Agnes 5 Longfellow 4B .... Mt. Eden Mixed . Raphael Weill 2A . . . . Sunnyside 6A -Bot. 37 39 31 SO 39 50 31 27 Poly. High School L2 18 Grant 7A . Hamlin Jr.-Sr.- Lincoln 5 A Parkside 4B Geary 3B Poly. High School L2 Guadalupe 6A Paul Revere 3B Paul Revere 4A Knightsen 7-8 Cabrillo Kindergarten . Corpus Christi 6-7 Notre Dame H. S Secretarial ... Fremont H2 Lowell High 10th Redding 4A-4B St. Joan of Arc 6-7-8th Central S-6th Lincoln 2-3d Bryant 4B Bryant 3A Hawthorne 5B Commodore Stockton 4B Burbank H8 St. Peter's 3d-4th 46 12 26 28 31 19 32 39 38 31 46 60 41 30 5 78 101 46 54 29 40 33 35 28 100 C. Benelisba L. Sweeney Sister Victorine Sister Benegne J. Kane Misses Oliver, Good A. J. Johnson Mrs. V. Kellcy Koehler R. N. Wilson S. Davis D. Rich C. T. Bothe H. Ekoos Koehler T. B. Cummings Evelyn Elster D. Christie A. McKinnon M. Springer Sister St. Joseph Sisters M. Donclson A. Schwartz Misses Gardiner Sister St. Joseph Adeline Field A. Hardy, B. Steel E. Leary M. Koenecke F. E. Nippert A. Barter H. M. Williams M. Roberta Vol. XIX] EVERM ANN— DIRECTOR'S REPORT FOR 1930 419 San Francisco Schools Visiting the Museum in 1930 — Continued Date 1930 May 27 u 27 u 27 u 27 u 28 u 28 u 29 u 29 June 4 " 5 " 9 « 9 " 9 " 9 (( 10 u 12 July 16 tl 22 » 25 Aug. 1 " 19 li 27 Sept. , 10 " 10 u 10 tt 14 u 16 u 17 u 19 u 19 u 20 u 23 a 25 H 25 u 26 « 26 Oct. 2 it 2 u 3 ti 3 u 6 tl 8 it 9 u 10 u 11 u 13 a 14 u 15 11 16 tt 16 11 16 tt 16 II 16 *' 17 « 17 « 17 n 17 Grade School E. R. Taylor 6A St. Agnes 7th, Commercial. Poly. High School L2 Polytechnic L2-Biology Garfield 4th Emerson 4B S. San Francisco 6th Junipero Serra 4B Crocker Jr. High H8 Sarah B. Cooper 6A S. F. S. T. College V. Zoology Woodrow Wilson Jr. H L9 Commodore Stockton 6B Commodore Stockton 6B Pacific Heights SB Jefferson 3B Teacher's College College 17 Teacher's College College 11 Number Pupils . 36 H . 74 20 . 40 . 50 . 38 . 35 . 60 . 20 . 31 . 30 . 15 . 37 . 30 . 33 . 33 Teacher's College Zoology Teacher's College Zoology Columbus 4A-B Raphael Weill 6A-6B Edison 4B Edison 4B Jefferson Eighth Raphael Weill IB Lafayette 3B Junipero Serra 2-4A, 5A . . . . Bernal 8B Lafayette 3B Emerson 6A Franklin 3A-2B Golden Gate 3A-3B-4A . . . Bay View Low Seventh. E. R. Taylor SB Grant 4A 19 17 29 33 30 36 34 26 36 86 37 38 32 38 75 35 34 44 Miss Ransom's 8th 11 U. of California Landscape Design 8 Parkside 2B 29 Emerson 6B 38 Girls High H8 Science 26 Central "! 3-4 44 Sherman 4A 31 Franklin L4th 40 Emerson 5A 13 E. R. Taylor 3B 29 Cabrillo 5B-6A 24 Sunnyside 6th 34 Laguna Honda 5B 32 Commodore Stockton 6A-6B 34 St. Ignatius College College 16 Presidio Jr. High 7th Grade 26 Laguna Honda 5A 37 Bay View 8B 27 Emerson 6A 38 Franklin Low 4th 29 Girls High HlO 28 Teacher Teping Sr. M. Martin M. S. Jussel M. S. Jussel C. McKeon H. Bain G. B. Gavin D. L. Baird M. Hibbard W. J. Karnes B. Kauntz M. D. Innes G. Morton M. Behn R. E. Dreyfus L. Nolan B. Kauntz B. Kauntz B. Kauntz B. Kauntz H. B. Grant H. Baxter C. Reed R. S. Miller M. H. Tray nor D. Thompson M. Harrington Ahlgren, Baird M. C. Beale L. C. Webb Miss Currid S. Hagerty L. King, M. Laug I. E. Loughlin L. E. Kamuff E. Johnson Regula Bernays H. W. Shepherd A. H. Ercolini A. E. Sharpe M. Pettit R. Grayson E. A. Shipaugh E. Callahan, G. Hill B. Fortune Olive Parker A. B. Green C. Benelisha B. Meyers L. Brovelli Geo. Haley O. C. Neimarkel E. Ohea R. I. Morrow D. Le Jeune Jessymae Dodge S. Ward 420 CALIFORNIA ACADEMY OF SCIENCES LProc. 4th Ser. San Francisco Schools Visiting the Museum in 1930 — Continued Date 1930 Oct. 17 II 20 II 20 " 21 " 21 (1 21 " 23 " 24 " 24 " 24 " 24 II 27 II 29 II 29 II 29 II 30 « 31 Nov, 3 " 5 " 5 " 8 II 8 " 10 " 13 " 14 II 14 11 19 " 20 Dec. 3 " 12 II 11 II 11 " 11 " 11 " 11 " 17 School Grade E. R. Taylor 6A Hawthorne 4th Hawthorne 2B-3A Frederic Burk 3d-4th Francis Scott Key 8th Girls High HlO . 35 . 39 17 . 31 . 36 All Schools Camp Fire 12 . 38 . 30 . 30 . 37 . 36 . 39 . 28 17 38 41 . 34 . 30 . 33 8 3 29 St. John School High School . Garfield 43 Garfield 4A Lafayette 4B Sarah B. Cooper 5th Guadalupe 5 A Monroe 7A Garfield Ungraded . . , Emerson 4A Hawthorne 5 A Frank M. McCoppin 3A-3B Bay View 7 A Jean Parker 6A Fairmont 6th Westlake Jr. High H9 Argonne 2d Galileo 19 30 27 13 30 30 Garfield 4A-4B Monroe 8A Roosevelt 18 Jean Parker 3d E. R. Taylor 4A State Teacher's College 21 Howard Avenue H8 24 State Teacher's College 24 State Teacher's College Freshmen 60 State Teacher's College Zoology 24 Laureau School H8 14 State Teacher's College Freshmen 20 Number Pupils Teacher 31 A. Simonetta Gertrude Flanagan M. Coen M. Gold A. Dowling S. Ward E. E. Boyes Sister Pauline C. McKeon A. McDonald T. L. Williams I. Brown S. Freer P. L. Plevin D. L. Darvill H. Bain M. Lahaney A. L. Barrett Ethel Maddocks May Casey I. Garwood M. Carmichael L. E. Andersen A. Kluegel C. McKeon E. H. Stern A. G. Soares M. Wramp Gwen Sellman M. Guernes W. E. Brown M. Guerrerd E. Pickard E. Pickard W. Naturik E. M. Fisher Schools Outside of San Francisco Visiting the Museum Date 1930 Jan. 10 tt 31 Feb. 1 " 4 " 28 Mar. 6 " 8 " 8 " 15 " 22 II 28 April 1 3 " 11 " 28 School Grade Menlo Park 3d-4th Washington, Alameda 8th 34 North Brae, San Bruno Nature Study. . Le Conte, Berkeley 6th Elem. School, Berkeley 3d Katherine Branson 2d Crocker, Daly City Sth Roseville, U. High Jrs.-Srs U. C. Berkeley Zool. 113 San Mateo, Jr. C Biology 32 Pleasanton 8th 25 Central, Redwood City 6th 30 Pittsburg 4-8th 1 70 Felton, S. Cruz Co 6-7-8 32 Number Pupils Teacher 34 Ivy Laughlin M. Snyder Grace Seeney S. Hamilton E. Norton Isabel Chesnut M. Packwood S. B. Fleming J. Grinnell Dr. Shepherd M. G. Noble Irene Crosby M. Ellis, Youngberg M. M. Oliver 12 21 26 6 a 13 27 Vol. XIX] EVERMANN— DIRECTOR'S REPORT FOR 1930 421 Schools Outside of San Francisco Visiting the Museum — Continued Date 1930 May 2 u 2 u 3 U 15 " 16 " 16 " 18 " 21 " 24 u 24 " 24 June 5 " 7 " 24 Aug. 14 " 4 Oct. 22 (1 30 " 30 u 31 Nov. 3 ii 14 " 14 " 21 " 21 Dec. 3 " 4 Ii 8 " 18 Number School Grade Pupils West Park, Tracy 44 Amer. Canyon, Napa Co l-8th. . Tech. High, Oakland Latin . . Jefferson, Colma 8th .... Irvington Grammar 8th .... Columbus, Berkeley 4th-Sth. Melrose, Oakland High 6th 19 Columbus 4th-5th-6th 65 Tamalpais Park 4th 30 Belvedere 7th-8th 10 Burbank, Berkeley H-7th 16 Jefferson, Colma 4th 32 Walnut Creek 6-7-8th 114 Laurel, Oakland Low 6th 52 Intermediate, Lodi 23 U. C. Berkeley 4A-4B 33 Edgemont, San Bruno 8th 37 Franklin, Berkeley High 4th 35 Franklin, Berkeley High 6th 45 Franklin, Berkeley Special 18 U. C. Davis Zoology 19 S. T. College, San Jose 2d 52 University High, Oakland 10th i 68 University High, Oakland L6th Visitacion Valley 5B-6A Weber College Jr. College .... Turnbull, San Mateo 6th-7th Lomita Park 7th-8th Burlingame, Y. M. C. A Teacher W. R. Hoar 45 V. Schebler, B. O'Hagan 60 H. B. Garrison 27 M. H. Tray nor 23 D. G. Scale 90 S. J. Irwin L. Bronner M. Wilson, Shapero Edna Maguire Myrtl;; D. Ensign C. McKinnon H. A. Madonna M. Parsons, C. Laggan S. Davidson E. F. Van Vlear E. W. Gifford Jane E. Trigg C. McEnerny E. J. Seabury G. Hillyard Tracy Storer E. C. Walsh Jean M. Nelson 86 E. Lucas 38 Helen Griswold 28 Eva Browning 33 H. J. Neuling 37 B. MacKenzie 22 R. Simrock Summary Schools of San Francisco: Total Number of Pupils 6526 Total Number of Teachers 208 Total Number of Classes . . ? 216 6526 Schools Outside of Sati Francisco: Total Number of Pupils 1676 Total Number of Teachers 47 Total Number of Classes 56 1676 8202 422 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Schools Visiting Steinhart Aquarium in 1930 Following is a list of the schools, the grades, teachers, num- ber of pupils, and dates of visits in 1930 : Schools of the City and County of San Francisco Date 1930 School Jan. 2 1 Geo. Peabody " 23 Pacific Heights " 31 Hawthorne Feb. 4 Sherman " 6 Le Conte " 6 Sarah B. Cooper ... 7 Sherman " 7 John Muir Grade Number Pupils Teacher 1 1 Alvarado . Mar. 1 3 Hawthorne 14 Columbus 14 Grant 14 Golden Gate 18 Jean Parker > 18 Jefferson 26 Hawthorne 28 Jean Parker 28 E.R.Taylor 1 Calvary Baptist Church 1 S. F. Sutro S C.R.Taylor 5 Columbus 6 Grant 8 Crocker School 10 Crocker Jr. High 1 1 Sarah B. Cooper 11 F. S. Key 1 1 Rincon 1 1 Polytechnic High 1 1 Polytechnic High 12 Parkside 12 Adams 12 Argonne 15 State Teacher's College 17 Immaculate Conception Acad. 18 Lincoln 18 Polytechnic 19 Polytechnic 20 Franklin 24 Commodore Stockton. 25 Sheridan 25 Lincoln 26 Edison 26 Edison 26 Edison 26 Raphael Weill 26 Presentation 2A-2B 34 3A 14 6B 36 6B 27 4A-4B 39 3A-3B 72 5B 33 Ungraded 14 5B 60 6A 46 6B 33 6A-6B 35 4A 27 4A 40 Kindergarten .... 39 5A-4B 35 5B-6A 36 3B 32 Juniors 9 Mixed 27 3A 27 3A-B 32 4B 38 High 5th 33 High 9th 30 Ungraded 14 4A 36 1B-2A-2B 24 L2 21 L2 27 2 A 25 2B-3A 24 8B 30 17 Ungraded 12 1B-2A-3B 62 L2 21 L2 15 Jun. Prim 22 4A 24 4A 29 Ungraded 10 6B 35 6A 25 6A 19 IB 24 7th & 8th 97 L. Roach Miss Greenwood F. C. Muller M. Doran J. Strassner C. MacCarra, F. Meachum M. Denny M. L. Kennedy G. P. Garety, R. Penn- feather C. Hackman J. W. Elkins Mrs. R. N. Wilson M. Maughan C. Seidkin D. Dacatur M. E. Doherty Norma Valsangiacomo K. M. Brazill Mrs. K. R. Camp Florence Wiggins A. Wilcox M. K. Schiullger E. Johnson Mrs. Peck wood Miss M. E. Hibbard P. Stauer C. Schell M. Quinn M. S. Jussel M. S. Jussel A. H. Ercolini Alma McVeigh D. Boyisen L. Reid Sister Margaret Mary Mrs. R. D. Love. Miss Jane Redmond E. Koehler E. Koehler Marie A. Reilly Mrs. H. Jacobs M. A. Lentz Mrs. F. A. Buerly M. Kelly J. O. O'Brien A. Wilson M. Villalon Sister M. Genevieve Vol. XIX] EVERMANN— DIRECTOR'S REPORT FOR 19 SO 423 San Francisco Schools Visiting Steinhart Aquarium in 1930 — Continued Date 1930 Mar. 26 U 26 it 27 u 27 - 28 u 28 u 31 u 31 April 2 u 2 " 3 " 3 " 3 " 4 u 4 u 7 il 8 u 8 u 9 u 9 u 10 u 10 « 10 " 11 " 12 t( 23 u 25 It 25 u 29 u 29 u 29 " 30 May 6 " 8 a 9 u 13 u 14 It 14 It 16 u 16 11 19 u 19 u 21 u 22 u 22 School Grade Lowell H2 Edison 6B Sunnyside 5 A Com. Stockton 4B-4A Nlthber Pupils . . 10 L . 35 . 36 . 58 Teacher Elskamp Presentation 3-4-5-6 . Argonne 2A .... Lafayette 7-8 . . . . Com. Stockton SB . . . Bemal 7B . . . . Madison 2B . . . . Bemal ; 7A . . . . Paul Revere 5 A ... . George Peabody 3A . . . . John Muir 3B-4A. Washington Irving 6A .... Monroe .-. 5 Fremont H6 . . . . Polytechnic L2-H2 . Dudley Stone Special. Frank McCoppin 8B Sarah B. Cooper 6B . . . . Guadalupe 3A . . . . Bryant 4-5 . . . . Marshall 3 A 85 36 10 38 34 32 35 37 32 54 40 36 37 19 ii 21 20 28 27 28 Jean Parker 12 Sunnyside 6B . Sarah B. Cooper 2 . . Emerson 3A . Jefferson 2B . Golden Gate 2 A . St. Agnes School 5 . . 37 25 28 27 25 50 Polytechnic High H2 Biol 21 50 39 65 44 28 26 45 38 9 60 50 54 57 E. R. Taylor 1 Longfellow 4B Washington Irving 6B-5B Grant 7 A Parkside 4B Lincoln 5 A Cabrillo Kindergarten . Paul Revere 4A St. Pauls :. . . 6-7 Corpus Christi 6-7 Lowell High 10 Lincoln 2-3 Alvarado 4 A 22 Redding 4A-4B . 22 Washington Irving 3B 23 Bryant 3A 23 Bryant 4B 23 Commodore Stockton 4B 23 Hawthorne 5B 26 St. Peters 3-4 ... . 27 Polytechnic L2-Biol . 29 So. San Francisco 6 76 40 40 29 35 33 100 40 35 M. M. Hardiman F. Kelly Mrs. Richter, Miss Hol- land Sr. M. Gabrielle F. Stockton M. Copeland L. Mitchell Olive Alida Perry M. Kilgariff B. Kelly M. J. Luding E. D. Ruff Z. Meyer, F. Bleuler Florence R. Mclnerney M. Cunningham S. A. Perry H. J. Wilcox Mrs. Jones, Miss Mosby H. Davis M. D. Roache B. Cole L. Moncrieff N. Mack V. Duane Mrs. C. Benelisha J. Antipa I. McCauley E. K. Hills Elva La Rue Sr. M. Benigna L. M. Gladstone H. Downey, F. Geistofson J. Kane Miss Doyle, Mrs. Dolan R. N. Wilson C. T. Bothe Dorothy Rich M. Springer D. Christie Sr. M. Alphonsus Sisters of St. Joseph A. Schwartz D. B. Steel, Alice Hardy M. O'Shaughnessy, E. Crawley S. M. McMackin, G. Gardner E. Cummings M. Koenecke E. Leary A. Barter Florence E. Neppert Srs. M. Roberta & Edward M. S. Jussel G. B. Gavin 424 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. San Francisco Schools Visiting Steinhart Aquarium in 1930 — Coniinued Date 1930 May 29 " 29 " 29 " 29 June 2 2 3 3 " 4 5 5 6 " 9 " 10 " 12 July 25 Sept. 5 " 10 " 12 " 17 18 18 19 19 20 25 26 26 27 3 3 6 10 14 17 17 17 20 20 20 21 21 24 24 24 27 27 29 29 29 30 30 30 31 Oct. School St. Agnes 7. Grade Number Pupils . 50 Garfield Emerson Junipero Serra. Monroe Fairmount . . . . 4A-4B . 4B. . . 4B.... 8A. . . 7A. . . Laguna Honda Monroe Monroe Laguna Honda Sarah B. Cooper Park Boulevard Private School Commodore Stockton Pacific Heights John Muir McKinley Orphanage Cabrillo Edison Grant Junipero Serra Frederick Burke Lafayette F. S. Key Lafayette Emerson Bay View Grant E. R. Taylor So. San Francisco Grammar. Frederick Burke Emerson Daniel Webster Hancock V'isitacion Valley E. R. Taylor Bernal Bay View Jefferson Hawthorne Bernal Francis Scott Key Hawthorne Girls High Garfield Garfield Sarah B. Cooper Girls High Monroe Guadalupe Garfield John Swett Junior High Alamo Emerson Hawthorne 8A 7A 8A 7B 6A 1 A- Kindergarten . 63 SB 2A 4B. . 4B. . IB. . 2-4 A. 50 38 59 30 57 19 41 31 14 31 20 66 33 40 38 34 65 28 86 L5 37 IB 32 6B 29 3B 38 6A 32 L7 35 4A 44 5B 34 H4 10 HS-L6 16 6B 38 Ungraded 13 5A-5B 62 4A-B 25 6A. 7A. 8B. 6B. 4.. 73. 8. . 31 32 25 38 35 35 31 2B-3A 37 HIO 25 4A 30 43 .?0 5 36 HlO 27 7A 28 SA 39 Ungraded 16 L8 30 5A-5B 33 4A 38 5A 39 Teacher Srs. Margaret Mary and Martina M. Ivancovich H. Bain M. Ahlgren, D. L. Baird C. A. Davis Mrs. Holden, Miss Corp- stein Mrs. Rae, Miss Lynch D. Greenwood E. E. Meline Miss Feehan, Mrs. Rae W. J. Karnes Blanche R. Miller G. Morton, M. Behm R. E. Dreyfus Z. Coyle. M. La Gomarsin Marion Sommerin J. Hampton R. Miller, C. M. Reed A. Tiling M. Ahlgren, D. L. Baird and G. E. Bell Miss Denhard Mrs. Williams E. M. Holchester L. Webb Miss Currid Ida E. Loughlin E. Johnson L. E. Kamuff Miss Broncr Miss Raemsch A. E. Sharpe Miss C. Cuneo Mrs. AUmon, Mrs. English F. Flinn A. Simonetta E. L. Murray Rose I. Morrow M. Shepston Gertrude Flanagan Mildred Cavanagh A. Dowling Mrs. M. Coen S. Ward Alice McDonald C. McKeon L Brown S. Ward P. L. Plevin S. Frees D. Dorsill Miss Woodward H. Searight H. Bain M. Lahaney Vol. XIX] EVERM ANN— DIRECTOR'S REPORT FOR 1930 425 San Francisco Schools Visiting Steinhart Aquarium in 1930 — Continued Date 1930 Nov. 5 u 5 u 6 u 7 « 10 u 13 a 13 11 13 " 14 " 14 " 14 « 14 11 18 it 18 (( 18 ii 19 (I 19 u 20 » 21 '* 28 Dec. 4 " 6 " 10 11 11 11 12 K 17 School Grade Jean Parker 6A Bay View 7A Argonne 3A Bemal 8A Argonne 2 Garfield 6B Monroe 7A-B Number Pupils Teacher 3i 28 27 34 29 25 86 Garfield 6A 29 Monroe 8A 26 Garfield 4A-4B 52 Irving M. Scott 2A-2B 28 I.M.Scott 4B-5A 29 Roosevelt L8 43 Polytechnic High School L2 28 Roosevelt L8 40 Roosevelt L8 42 Polytechnic High H2 21 Jean Parker 3A-3B 30 Visitacion Valley 5B-6A 36 Woodrow Wilson 7 25 St. Joan of Arc 5 22 South San Francisco 6 40 State Teacher's College 1 20 State Teacher's College . State Teacher's College Immaculate Conception Acad. Sunnyside lA-Zool 75 Freshmen 20 11 30 7B 20 May Casey Ethel Maddocks O. On- Silvia Kresteller L. E. Andersen Mrs. Scott Misses Greenwood and Davini J. A. Boyle E. H. Stern C. McKeon, B. Kagel Mrs. H. McCourt Lucille Koenig A. G. Soares M. S. Jussel A. G. Soares A. G. Soares Wilcox Mrs. P. A. Wramp Helen Griswold Mrs. Nellie L. Raper Sisters of St. Joseph G. B. Gavin Mrs. Gueseno Edith A. Pickard, Edna Fisher and Mrs. Gueseno M. Fisher Sister M. Celestine M. Hoeft ,'^>^^008~^^X<^ Date 1930 Jan. Feb. Mar. 10 23 31 1 1 4 4 6 7 8 8 15 21 21 21 23 28 Schools Outside of San Francisco Visiting Steinhart Aquarium in 1930 School Grade Number Pupils Teacher Menlo Park School 3-4 34 North Brae, San Bruno 6-7 41 Washington, Alameda 8 34 Edinvale, Hayward .^. . 5-6 5 Boy Scouts, Mill Valley Troop 2 17 Le Conte, Berkeley 6 21 Livermore High School 23 Katharine Branson School, Ross 2 6 University Elementary School, Berkeley 5 32 Stanford University, Palo Alto. Medical 12 Roseville Union High 3-4 13 U. C, Berkeley Zool. 113 27 Walnut Creek, Walnut Creek. . 6-7-8 82 Lafayette, Lafayette 7-8 27 Columbus, Berkeley 6 45 Portola School, Portola 1-8 40 Pleasanton Gram., Pleasanton . 8 25 Ivy M. Loughlin Miss D. Jones M. Snyder Mrs. R. N. Dwinell R. C. Sproleder S. Hamilton O. Murphy Isabel Chesnut Mrs. A. S. Gist Dr. Starks Mrs. Sana, B. Fleming J. Grinnell Mabel E. McLoggan Mrs. Clara Christian Miss Hogan, Miss Almy Miss Crosby Mrs. Gertrude Noble, V. Bernard Johnson 426 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. Date 1930 April 8 " 11 " 12 " 17 May 2 " 2 5 " 9 10 IS 15 16 16 17 21 21 22 22 23 24 24 25 4 5 6 7 9 June " 10 " 20 " 24 Aug. 23 " 28 " 28 Oct. 8 10 16 17 22 30 31 Schools Outside of S.-^n Francisco Visiting Steinhart Aquarium in 1930 — Continued School Daniel Webster, Oakland . . Pittsburg Grammar School . E. Morris Cox, Oakland. Knightsen Grade 7-8. Number Pupils 16 D . 175 H6 2-3-4-5 . American Canyon, Napa Jet. . . 1 to 8 43 West Park, Tracy. Prescott, Oakland. Mt. Eden Sept. 11 " 13 " 26 " 27 Adv. Orchestra . . 6 4-5-6-7-8 Westlake Junior High, Oakland Scotts Valley, Santa Cruz Jefferson, Colma Knightsen, Knightsen Columbus, Berkeley Melrose, Oakland Columbus, Berkeley Notre Dame, San Jose Central, San Mateo Emerson, Berkeley Mt. Eden, Mt. Eden Tamalpais Park, Mill Valley. . . Craginont, Berkeley Jefferson School, Colma St. Mary of the Palms, San Jose Jefferson, Colma San Rafael Grammar Mission Grammar, San Jose. . . Woodrow Wilson, Jr. High, Oakland St. Vincents, Vallejo Jefferson, Oakland Laurel, Oakland Calvin Coolidge School, Burlingame Wildwood, Piedmont Calvin Coolidge School, Burlingame H7, . 5-8. . 8 7-8.. 4-5 .. , H6. . 4-5-6. Secretarial 37 5-6 6B 1-2-3 4 4-5 4-5 7-8 4 L8 8 Teacher Husing A. Huganey, W. Yoren- berg, W. Ellis 17 M. E. Geary 30 Mrs. E. Moody, Miss Agnes Prey Virginia Schebles, Berna- dette Hays 43 Ernest Dobney 34 Miss Campanari 50 Mrs. Overacker, Mrs. Good, Misses Oliver and Garsberger 10 Grace M. Taylor 20 Ruby Owens 26 M. H. Traynor 31 Anne McKinnon 90 S. J. Irwin 19 Lydia Bronne 66 Mrs. Wilson and Shapero Sister M. Reginald 44 A. G. Field 42 A. M. Meginnes 48 Edna S. Overacker 30 Edna Maguire 15 Harry H. Stoops 26 Miss Doolin 30 Marion Burton 32 Hazel A. Madonna 22 C. F. Timony 16 J. B. Vasconcellos L9 15 8 28 Mixed 23 L6 22 H3. 42 Jefferson, Colma Highland School, Oakland. . . . Corralitos Union, Watsonville. Presbyterian Sunday School. Mountain View Central, San Mateo Franklin School, Berkeley. . . . 8 34 6A-6B 32 7-8 22 Lincoln School, Berkeley. Franklin, Berkeley Edgemont, San Bruno . . . Franklin, Berkeley Franklin, Berkeley 3-4. L4. 23 44 40 Special 17 L4 29 8 34 H6-H4 80 Special 18 M. D. Innes Sr. Beockmans Grace W. Janoschik S. H. David.son 42 Elinor H. Statler 18 Agnes Rathbone Mrs. C. C. Kerson, Elinor H. Statler Marie H. Traynor Marie L. Spenser Elma G. Bradley Miss Center Reinecke and Grayson Edna M. Callahan, Grace Hillyard Charlotte Hayford Mrs. Dodge Jane E. Trigg Mrs. vSeabury Cianciarulo and Hillyard Vol. XIX] EVERM ANN— DIRECTOR'S REPORT FOR 1930 427 t Schools Outside of San Francisco Visiting Steinhart Aquarium in 1930 — Continued Date Number 1930 School Grade Pupils Teacher Nov. 3 Univ. Calif., Davis lA-Zoology 25 Tracy I. Storer " 14 State Teacher's College, San Jose 2 52 Elizabeth Cameron Wilde " 21 University High, Oakland LIO 86 E.Lucas Dec. 3 Weber College, Ogden, Utah. . . Jun. College 28 Eva Browning 4 Turnbull, San Mateo . 7-H6 33 Harry J. Neuling " 9 Lazear School, Oakland 5-6 14 Rena Lesser " 1 1 Lawrence School H8 14 Warren Naturich " 1 1 Howard, Burlingame 8 24 William E. Brown " 15 Girl Scouts, Burlingame 18 Mrs. W. H. Cortelyou Summary Schools of San Francisco: Number of Visiting Pupils 6320 Number of Visiting Teachers 218 Number of Visiting Classes 221 Schools Outside of San Francisco: Number of Visiting Pupils 2353 Number of Visiting Teachers 85 Number of Visiting Classes 101 Department Activities The year has been marked by commendable activity in the respective departments, as is evidenced by the annual reports of the several curators. In the Department of Botany the growth has been up to the normal; the number of herbarium sheets increased from slightly in excess of 171,000 in 1929 to more than 180,000 at the end of 1930. The various additions to the Herbarium will be found listed by the Curator in her departmental report. Collections were made by, or received from, members of the staff and from friends of the department from many different localities; all of which are fully recorded in the Curator's report. The California Academy of Sciences was represented at the Fifth International Botanical Congress which met in Cam- bridge, England, in August, 1930, by regularly appointed dele- gates as follows : Miss Alice Eastwood, Curator of Botany, California Academy of Sciences, voting delegate; Dr. Willis 428 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. L. Jepson, Professor of Botany, University of California; Dr. Douglas Houghton Campbell, Emeritus Professor of Botany. Stanford University; and Miss Susie M. Peers, Secretary. Board of Trustees, California Academy of Sciences. Besides attending the Botanical Congress, Miss Eastwood also attended the sessions of the International Horticultural Congress which met in London ; she also took advantage of the opportunity to spend considerable time in the Herbarium of the British Museum and in the Royal Herbarium at Kew. where she examined certain collections of plants obtained in America. She visited several botanic gardens for the purpose of studying the fuchsias, a group in which she is now espe- cially interested. The Department of Entomology continues to grow under Mr. Van Duzee's wise and enthusiastic supervision. During the year the research collections increased by 20,694 speci- mens, a detailed statement of which is given by the Curator in his report. The laboratory of this department continues to be a popular meeting place for the local entomologists for the examination and study of species in which different ones are interested, for exchange of views, and for discussion of special problems in the field of entomology. Among prominent entomologists who have devoted considerable time each week to research work in the department's laboratories are Dr. F. E. Blaisdell, Dr. E. C. Van Dyke, Mr. E. R. Leach, Mr. L. S. Slevin. and Dr. Vasco M. Tanner. Among young entomologists who come quite regularly to the department for special research may be named Gorton Linsley, Graham Pleid, Jas. E. Coute, Rev. Edward Guedet, Eric Walther, Geo. R. Wilson, R. Blackwalder. Carl D. Duncan, H. H. Keifer, Robert Usinger, Dr. Paul W ilbur, E. C. Zimmermann, and T. O. Zschokke. For the Department of Exhibits the year was a very active one. All of the habitat groups and other public exhibits were gone over carefully to see that they were not suffering in any way. Early in the spring (May 27), Mr. Tose, the chief of this department, left San Francisco to join Mr. Leslie Simson in Africa for the purpose of collecting accessory materials and making sketches for the use of the artists who will jiaint the Vol. XIX] EVERMANN— DIRECTOR'S REPORT FOR 1930 429 backgrounds for the habitat groups of African game animals which Mr. Simson is now collecting for the Simson African Hall that will form the principal unit in the Academy's new building, construction work on which is just now beginning and which, it is hoped, will be completed next October. The Library, under the supervision of the Assistant Li- brarian, Mr. Thomas Cowles, has made satisfactory growth. Mr. Cowles has been active in completing the Academy's file of important serial publications of learned societies and scien- tific institutions. With the cooperation of the curators of the respective departments the growth of the Library has been as rapid as our funds would permit. It is a matter for deep regret that the income of the Academy does not permit a larger allotment for library pur- poses, a condition which obtains in an equally great degree with the other departments. Mr. H. Walton Clark, Assistant Curator, Department of Fishes, devoted much of his time to curatorial work such as transferring the Jordan-Eigenmann Indiana University collec- tion to permanent containers, re-bottling, labeling, arranging, and supplying with fresh alcohol and new labels where necessary. Similar attention has been given also to the general collec- tion. Arrangements ha\'e been made with Mr. George S. Myers whereby he will study and report upon certain portions of the Ternetz collection. Mr. Myers has already begun that study and will probably have his report completed within a year from now. It is expected that the East Wing of the Museum will be completed by the end of 1931, when the Department of Fishes will be moved into the basement under the Simson African Mammal Hall of that building, where commodious and excel- lent quarters will be found. The Department of Herpetology has had a successful year, as is shown by the report of the Curator, Mr. Slevin. At the beginning of the year Mr. Slevin was still in Australia. He left Australia February 22, 1930, and returned to America March 13. The expedition resulted in the addition of speci- 430 CALIFORNIA ACADEMY OF SCIENCES [Pkoc. 4th Ser. mens to the Academy's herpetological collections, which now number by actual count 66,722. The Department of Ornithology and Mammalogy, as may be seen from the Curator's report, has had a satisfactory year. The accessions have been many, considerable field work was done, and much important research work was accomplished. The outstanding event of the year was the visit of Curator Swarth to London and Tring to study Galapagos finches in the British Museum and the Rothschild Museum, and to Am- sterdam where he attended the Seventh International Orni- thological Congress, June 1-8. Another matter of general interest was the completion by Curator Emeritus Mailliard, and the publication bv the Academy, of an attractive and very useful handbook on The Birds of Golden Gate Park. This publication supplies a long- felt want for a handbook of the birds of the Park. Mr. Mail- liard's book meets this need admirably. The Aquarium has not lost any of its popularity with the public, as may be seen from the record of the number of visitors, and the comments wdiich are heard and the letters received. The report of Superintendent Seale shows that the number and kinds of fishes and other animals on exhibition compare favorably with those of the previous year. The Matson Navigation Company continues to cooperate with the Academy by bringing fishes to the Aquarium from the Hawaiian Islands, from Samoa, and from Australia. The specimens from Samoa are particularly beautiful. There are so many more species of fishes and other aquatic animals that would make very attractive and instructive ex- hibits, and which we can not now display because of lack of sufficient space, that the Aquarium should be enlarged. Presi- dent Grunsky has presented the matter to the City Supervisors and it is hoped that favorable consideration may be given to the recommendation. The Department of Paleontology had a satisfactory year. Because of lack of space for housing collections, field activi- ties primarily for the purpose of securing research material were confined to tho.se necessary in connection with work already begun for which additional material was needed. Vol. XIX] EVERMANN— DIRECTOR'S REPORT FOR 1930 43 J With the construction of our new building and the transfer of the Department of Entomology to it, the rooms now occupied by that department will be assigned to the Department of Paleontology, which will give Paleontology quarters which will prove very satisfactory and ample for several years to come. The members of the stafif of this department continue to be in demand by oil companies who wish their assistance in field investigation. Assistant Curator Hertlein was loaned for sev- eral months to the Hudson's Bay Oil and Gas Company to carry on geological explorations in Alberta, which afforded Dr. Hertlein opportunity to obtain considerable collections of Cretaceous fossils from that region. Many students from various parts of the country visited the department during the year and made use of the collections in connection with studies on which they were engaged. The department continues to help specialists by loaning cer- tain specimens or collections which they need to examine in their special studies. The acquisition of the large Baldwin collection of mollusks by the Department of Paleontology in 1928 has been briefly noticed in preceding reports. The full value of it could not be realized until some progress had been made in unpacking and installing it in the Academy's research series. This work has now been practically completed and the collection will stand as an indelible monument to the industry of this early Hawaiian collector. In connection with the checking of records pertain- ing to the collection some very interesting biographical notes were compiled by Messrs. Hanna and Church. These are repro- duced in full below. David Dwight Baldwin, 1831-1912 By G. D. Hanna and C. C. Church In 1928, the California Academy of Sciences received as a gift from his heirs, the large and varied collection of shells of the late D. D. Baldwin. The collection consists of land and fresh water shells from various parts of the world and especially marine, fresh water and land shells of the Hawaiian Islands. One large case of May 29. 1931 432 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. marine shells was exhibited at the Alaska- Yukon-Pacific expo- sition at Seattle, Washington, in 1909 and was awarded a gold medal. The Hawaiian land shells are represented by a con- siderable number of the beautifully varied tree and ground snails famous among conchologists the world over, for their bright colors and intricate design. During all the years in which he was collecting shells on the islands, Mr. Baldwin's own family was only mildly interested in his work, but sometimes they did help him collect, and his oldest son E. D. Baldwin, a surveyor, was sufficiently interested to do some good collecting on his own account. However, in his will, Mr. Baldwin made it known that he wished his ovvU family to have the collection which they had made together. To each member he willed the part in which he or she had been most interested. To Mr. E. D. Baldwin he gave the bulk of the Hawaiian land shells; to Mrs. Lilian B. Atwater and Mrs. Duncan B. Murdoch he gave the marine shells, and the land and freshwater shells from other parts of the world he gave to Mrs. Winifred B. Weddick. Soon after this disposition was made the Bishop Museum of Honolulu acquired the collection of land shells received by E. D. Baldwin, but the remainder of the collection, left at the Haiku home after the break-up of the family, was passed un- noticed and forgotten. It was not until 1928 that the junior author, in a chance conversation with Mrs. W^inifred Brewster (now Mrs. Morrison), a granddaughter of D. D. Baldwin, learned of the collection. An effort was then made to bring it to light and through the hearty co-operation of Mrs. Morrison and the heirs mentioned above, the collection (with the excep- tion of the part secured by the Bishop Museum), was recovered from the old deserted Haiku house, packed and sent to the Cali- fornia Academy of Sciences. Miss Lucie Hicks acted as repre- sentative for the Academy in going to Maui, meeting the donors and in arranging for packing and shipping. Mr. Dun- can Murdoch did the greater part of the hard work of crating the cases and assisted Miss Hicks in the packing. Mr. and Mrs. Murdoch and Mrs. Weddick are to be especially commended for the kindly reception given Miss Hicks. Dr. H. A. Pilsbry has assisted us in compiling the bibliography given below. Vol. XIX] EVERMANN— DIRECTOR'S REPORT FOR 1930 433 In view of Mr. Baldwin's work in the Hawaiian Islands, not only as a collector in the field of Botany and Zoology, but as a pioneer in education and agricultural development, we believe it to be of timely interest to set forth the salient features of his long and varied career. David Dwight Baldwin was born at Honolulu, November 26, 1831. His father, Rev. Dwight Baldwin, M. D., was originally from Durham, Conn., and came to the islands with the fourth band of missionaries which left New Bedford, Mass., Decem- ber 28, 1830, and sailing around Cape Horn, arrived at Hono- lulu June 7, 1831. Rev. Dwight Baldwin had graduated from Yale College in 1821 and Auburn Seminary in 1829 and it was only natural that when his son had completed his work at Punahou School, Honolulu, he should go on to Yale. In 1852, he sailed east around Cape Horn and, arriving at New Haven, was admitted to Yale the next year. He graduated from that institution in 1857 with the A. B. degree and the honor of having won the De Forrest astronomical prize. The winning of this distinction in astronomy is the first indication we have of his scientific inclinations. On October 7, 1857, he was married to Lois Gregory Morris, a descendant of Robert Morris, famous financier of the Ameri- can Revolution, and shortly afterwards the couple set sail for the Hawaiian Islands. The young huband's knowledge of astronomy was to be of invaluable service to the party on this trip, for soon after embarking he discovered that the captain of the ship sailed only by "dead reckoning." From then on to the end of the long cruise he navigated the ship and delivered the party safely into the harbor of Honolulu. This date marks the beginning of Mr, Baldwin's active life on the islands. From 1857-1864 he was a cane planter at Lahaina, Maui, and two of these years (1861-1862) he was a member of the Hawaiian legislature. From 1865 to 1872, he was manager of the Kohala Sugar Company, from which he resigned to go back and spend another year at Yale. While attending school he worked as librarian of the law school and received his M. A. degree in 1874. On his return to the islands in 1874 he was made vice- principal of Lahaina School. His work there must have been very satisfactory, for in 1877 he was appointed Inspector- 434 CALIFORNIA ACADEMY OF SCIENCES [Proc. 4th Ser. General of Schools under the monarchy, a position which he held for eight years. His work earned for him the title of "Father of English Education in Hawaii." He was first to introduce English as a basis of education in the schools of Hawaii. In 1885 he was made vice-principal of Lahainaluna School and held the position until 1890, when he moved to Haiku, Maui, to become principal of Hamakuapoko School and pioneer pineapple planter of Maui. From 1903 to 1912 he was vice- president of the Haiku Pineapple Company. He died June 16, 1912, at Honolulu. Notice of his death was published in The Nautilus, vol. 26, August, 1912, and a brief account of his life with a portrait was published the following November in the same journal, vol. 26, 1912, pp. 82-83. About the year 1850, when Mr. Baldwin was a very young man, an active interest in the collection of land shells was awakened in the islands. Many collectors entered the field and it is quite probable that at this time he did his first systematic work. This period of land shell excitement is still known in the . islands as the period of "the land shell fever." It lasted for several years and we know that by 1852 when the young man left Oahu to go to Yale, he had made a considerable collection of shells. While in school at New Haven he must have studied and developed an interest in botany, for on returning to the islands in 1851 he devoted much of his spare time to the study and collection of the native ferns and mosses ; however, he did not ne