PEABODY MUSEUM OF NATURAL HISTORY, YALE UNIVERSITY NEW HAVEN, CONNECTICUT, U.S.A. A NEW OREODONT FROM THE CABBAGE PATCH LOCAL FAUNA, WESTERN MONTANA

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Postilla PEABODY MUSEUM OF NATURAL HISTORY YALE UNIVERSITY NEW HAVEN, CONNECTICUT, U.S.A. Number 85 September 21, 1964 A NEW OREODONT FROM THE CABBAGE PATCH LOCAL FAUNA, WESTERN MONTANA STANLEY J. RIEL PEABODY MUSEUM OF NATURAL HISTORY, YALE UNIVERSITY INTRODUCTION Mammal-bearing beds on the north side of the Clark Fork River east of Drummond, Montana, were first noted by Earl Douglass in 1901. In his discussion of the fossils collected from this site, Douglass (1903, p. 151) called these beds "doubtfully Oligocene" and wrote, "Only three good specimens were obtained here and none of these can I identify with species found elsewhere." Little more was said of the locality until the late 1950's when three more fossils were found. The formal designation of "Cabbage Patch Local Fauna" was made by Konizeski and Donohoe (1958) after "the only, but adequate, neighborhood bar." The Cabbage Patch locality is three miles east of Drummond, Montana, on the north side of the Clark Fork River (figure 1). The beds extend for at least two miles east and north of U.S. route 10 but are largely covered by gravels and vegetation. The specimen of Desmatochoerus described in this paper was found by the author in Sec. 10, T. 10 N., R. 12 W. I wish to thank Robert W. Fields for permission to borrow the specimen from Montana State University and for his aid in field

2 Postilla Yale Peabody Museum No. 85 Figure 1. Index map of Cabbage Patch vertebrate fossil locality. recovery. I would also like to thank Elwyn L. Simons and James A. Hopson of Yale for helpful comments and criticism. The tooth nomenclature is that used by Schultz and Falkenbach

Sept. 21, 1964 A new oreodont from Montana 3 (1941, figure 17 and 1956, figure 4). The following is a list of the abbreviations used in this paper: CNHM Chicago Natural History Museum F:AM Frick collection, American Museum of Natural History MSU Montana State University YPM Yale University, Peabody Museum of Natural History DESCRIPTION AND DISCUSSION OF AFFINITIES FAMILY MERYCOIDODONTIDAE Thorpe, 1923 SUBFAMILY DESMATOCHOERINAE Schultz and Falkenbach, 1954 GENUS DESMATOCHOERUS Thorpe, 1937 Desmatochoerus macrosynaphus*, sp. nov. (text-fig. no. 2; plates I, II) Holotype: MSU 0940; a mandible with I 2 -M 3 ; partial upper dentition including right P 3 -M 3, left C, P 2, P 3, M 3. Hypodigm: Type only. Plastotype: YPM 20957. Diagnosis: Medium size; alveolar length of lower dental series approximately 135 mm; mandible very long and narrow; elongate symphysis extending to beneath Mi; ramus very shallow anterior to M 3, increasing in depth posteriorly with abrupt downward curve of inferior border beneath M 3 ; dentition light as in D. (Paradesmatochoerus); superior premolars narrow; M 3 with prominent metastyle; lower premolars not crowded; posterior accessory blade present on P 3 ; anterior and posterior fossettes of P 4 open lingually. Discussion: In their Revision of the Oreodonts, Schultz and Falkenbach (1954) divide species of Desmatochoerus into two groups. One of these groups is assigned to a new subgenus; the * From the Greek macros (long) and synaphe (connection) in reference to the symphysis of the mandible.

4 Postilla Yale Peabody Museum No. 85 other group is without subgeneric designation and is referred to as Desmatochoerus. The subgenus, D. (Paradesmatochoerus), includes small species with dentition more brachyodont and lighter than in Desmatochoerus. In these characters the present specimen is similar to species of that subgenus. In tooth pattern, length of symphysis and shape of the lower jaw, however, D. macrosynaphus is considerably different. In the author's opinion, these differences are great enough to warrant its assignment to at least a new subgenus. However, because the species is based on a single specimen, such an assignment would be more or less equivocal and would be of dubious taxonomic value. Thus, no subgeneric designation has been made. The teeth of the type specimen of D. macrosynaphus are considerably worn but, in most, the dental patterns have not been obliterated. The pattern of the superior dentition, insofar as can be determined, is similar to that of YPM 13957, the type of D. hatched grinnelli (see Schultz and Falkenbach, 1956, figure 7, and this report, plate II). P 2 and P 3 are more square in D. hatched grinnelli, however, than in the type of D. macrosynaphus where these teeth are considerably longer than wide. The species also differ in cingula development. Cingula are especially well developed on the lingual sides of P 4 -M 3 of D. hatched grinnelli. On D. macrosynaphus, cingula are present only on the anterior sides of M 2 and M 3. The lower molars do not differ greatly in members of the genus except in size and minor differences in cingula. Premolars 3 and 4, however, show considerable variation. Comparative patterns of D. macrosynaphus, D. hatched grinnelli, and D. (Paradesmatochoerus) wyomingensis are shown in figure 2. As can be seen in this figure, the posterior accessory blade on P 3 of D. macrosynaphus is blade-like and directed toward the median crest. In D. hatched grinnelli, this structure is short, more cuspate and connects with the posterior crest. On P 4 of D. macrosynaphus, the anterior and posterior fossettes are open lingually even though the tooth is considerably worn. On three relatively unworn YPM specimens of D. hatched grinnelli, these fossettes are completely closed. Judging from the worn teeth of the figured specimen of D.(P.) wyomingensis, the posterior fossette opened lingually in an unworn tooth. Division into anterior and posterior crescents,

Sept. 21, 1964 A new oreodont from Montana 5 which represents molarization of P 4, is much more distinct in D. hatched grinnelli and D. (P.) wyomingensis than in D. macrosynaphus. The coronoid processes of both sides of the mandible, the mental tubercle, and the right condyle are missing on MSU 0940. Enough of the jaw is present, however, to demonstrate that it is considerably different from other members of the Desmatochoeleft YPM 13957 MSU 0940 F:AM 33312 Figure 2. Comparative lower premolar patterns of Desmatochoerus. A) D. hatcheri grinnelli B) D. macrosynaphus C) D. (Paradesmatochoerus) wyomingensis (redrawn from Schultz and Falkenbach, 1954, figure 11.) rinae. According to Schultz and Falkenbach (1954, p. 177), species of Desmatochoerus are characterized by an elongate symphysis extending to below P 2 -P 4. The symphysis in the specimen described here is more elongate than in any other known oreodont, extending to below Mi. In Desmatochoerus, the inferior border of the ramus is more or less parallel to the tooth row anterior to P 4. In D. (Paradesmatochoerus), the ramus increases in

6 Postilla Yale Peabody Museum No. 85 depth between P 2 -P 4. In this character, D. macrosynaphus is similar to species of D. (Paradesmatochoerus). The inferior border is shallow anterior to M 3 with the depth of the jaw increasing only moderately. Below M 3, there is an abrupt downward curve of the inferior border. The angular region of the ramus is deep and prominent (see plate I). A mental tubercle appears to have been present below P 3 -P 4 but has broken off. The condyle is light and is not positioned horizontally, the external border being slightly higher than the internal border. TABLE 1 Measurements in mm Desmatochoerus macrosynaphus Upper right P 3 M 3 incl 81 P 3 P 4 M 1 M 2 M 3 Length 13.2 12 14.2 17 25.5 Width 11.4 13.8 17 19.5 22.4 Greatest depth of ramus below plane horizontal with alveoli... 71 Length of mandible at alveoli 225 Length of symphysis 85 Pi P 4 approx. 59 Pi M 3 approx. 134 P 2 P 3 P4 Mi Mo Ma Length 13 15.9 16.8 14 18 29 Width 5.7 8.6 12 11.5 14.5 15.5 NOTE ON STRATIGRAPHIC RELATIONSHIPS Little systematic collecting has been done from the Cabbage Patch locality. Several brief visits to the area by the author produced, in addition to the specimen described herein, only a few bone fragments and broken teeth. The faunal list known at present is given below (in part from Konizeski and Donohoe, 1958). Only single specimens of each have thus far been found.

Sept. 21, 1964 A new oreodont from Montana 7 Meniscomys sp.* Faunal list Cabbage Patch locality IMesocyon drummondensis Douglass, 1903 Kukusepasutanka schultzi McDonald, 1956 Diceratherium cf. armatum Marsh, 1875 Promerycochoerus (Pseudopromerycochoerus) minor Douglass, 1903 Leptomeryx transmontanus Douglass, 1903 Desmatochoerus macrosynaphus, new species These species known only from their types. * This specimen, CNHM Umll25, is listed as M. grassicarum by Konizeski and Donohoe (1958), but a description of the species has not yet been published. Douglass (1901, p. 2, 3) considered the Cabbage Patch beds as probable John Day equivalents. Schultz and Falkenbach (1949, p. 124) considered these beds as "approximately equal to the Harrison of the Great Plains." McDonald (1956, p. 642) quotes Schultz and Falkenbach's designation of a Harrison equivalent. Konizeski and Donohoe (1958) summarized the stratigraphic significance of the first six species of table 2 and tentatively correlated the Cabbage Patch Local Fauna with Wood's (1933, p. 2, 3) lower Madison Valley deposits as Rocky Mountain province equivalents of the Oregon lower to middle John Day. The specimen described in this paper apparently represents an aberrant species of the Desmatochoerus line and does little to clarify the age relationships of this fauna. According to the classification of oreodonts proposed by Schultz and Falkenbach (1954, chart 1), the range of the genus Desmatochoerus including D. (Paradesmatochoerus) is from late Oligocene to possibly late Miocene. Thus, an age assignment more precise than Arikareean for the Cabbage Patch beds must remain somewhat speculative.

No. 85 Postilla Yale Peabody Museum, PLATE I 1* V * \ v. I f. ' \ Right: Desmatochoeriis macrosynaphus. Holotype, 0940. Mandible, crown view, X 3 / 5. Left: Ventral view of the same, X 3/5. new species. MSU

Sept. 21, 1964 A new oreodont from Montana PLATE II S*fi Top: External view of left side of the same, X 4/9. Bottom: Crown view of the opper dentition, X 2/3, 9

10 Postilla Yale Peabody Museum No. 85 REFERENCES CITED Douglass, Earl, 1901. Fossil Mammalia of the White River beds of Montana: Trans. Amer. Philos. Soc, new ser., vol. 20, p. 237-279., 1903. New vertebrates from the Montana Tertiary: Ann. Carnegie Mus., vol. II, no. 2, p. 145-200. Fields, R. W., 1958. (Editor) Society of Vertebrate Paleontology, Guidebook, Eighth Field Conference, Western Montana: Mont. State Univ. Press, 50-f p. Konizeski, R. and Donohoe, J. C, 1958. Faunal and stratigraphic relationships of the Cabbage Patch beds, Granite County, Montana: In Fields, R. W., Editor, 1958, Guidebook, p. 45-49. McDonald, J. R., 1956. The North American anthracotheres: Jour. Paleo., vol. 30, no. 3, p. 615-645. Schultz, C. B. and Falkenbach, C. H., 1941. Ticholeptinae, A new subfamily of oreodonts: Bull. Amer. Mus. Nat. Hist., vol. 79, p. 1-105., 1949. Promerycochoerinae, A new subfamily of oreodonts: Bull. Amer. Mus. Nat. Hist, vol. 93, p. 73-198., 1954. Desmatochoerinae, A new subfamily of oreodonts: Bull. Amer. Mus. Nat. Hist., vol. 105, p. 147-256., 1956. Miniochoerinae and Oreonetinae, two new subfamilies of oreodonts: Bull. Amer. Mus. Nat. Hist., vol. 109, p. 373-482. Wood, H. E., 1933. A fossil rhinoceros {Diceratherium armatum Marsh) from Gallatin County, Montana: U.S. Nat. Mus. Proc, vol. 82, no. 7, p. 1-4.