Phyletic diversification of the Cormohipparion occidentale complex (Mammalia, Perissodactyla, Equidae), late Miocene, North America, and the origin of the Old World Hippotherium datum ; Bulletin of the American Museum of Natural History, no. 306
New York, NY : American Museum of Natural History
Study of the materials in the American Museum of Natural History that pertain to the taxon Cormohipparion occidentale Skinner and MacFadden (1977) reveals that at least six species are represented. This is based on data from the cranium, upper dentition, lower dentition, and mandible. The taxa embrace a period of time from about 12.5 Ma to 10 Ma. Major sites or faunas include the Dove Spring Formation (medial Clarendonian, California; Burge Local Fauna (early Clarendonian, Nebraska); Minnechaduza Fauna, Nebraska; MacAdams Quarry, Texas (early medial Clarendonian); Gidley Horse Quarry (late medial Clarendonian, Texas); XMas-Kat, Hans Johnson, and Machaerodus quarries (late medial Clarendonian, Nebraska); and Ash Hollow Formation (late medial Clarendonian, South Dakota). The name Cormohipparion occidentale is restricted to the larger of two species that occur contemporaneously in medial Clarendonian sites in Nebraska and, alone, at the Ed Ross Ranch Quarry, South Dakota. The second species in the XMas-Kat and related quarries is assigned to Cormohipparion matthewi, n.sp. A taxon from the Burge Local Fauna is assigned to Cormohipparion merriami, n.sp. Another taxon from the Burge Local Fauna is assigned to Cormohipparion johnsoni, n.sp. Materials from the Texas sites are allocated as Cormohipparion fricki, n.sp., and Cormohipparion skinneri, n.sp., from the MacAdams Quarry and Gidley Horse Quarry, respectively. Cormohipparion fricki, n.sp., also is represented in the Minnechaduza Fauna, Nebraska. Cormohipparion is restricted geographically to North America. Based on this review, Cormohipparion johnsoni, n.sp., is the most plesiomorphic species of the C. occidentale group of taxa. Cormohipparion quinni is a plausible ancestor (sister-taxon) for the C. occidentale group, but also persisted with it until about 12 Ma. During their radiation, elements of the C. occidentale group demonstrate an increase in upper cheek tooth crown height and complexity of the enamel pattern, as well as an increase in overall cranial size, with each species showing its own mosaic of parameters. The interval of 12.5-10 m.y. witnessed the initiation of a period of climatic cooling and an eventual expansion of vegetation communities toward more open associations, in part showing an increase in grassy areas. Apparently, the C. occidentale group developed and maintained a mixed-feeding adaptation to these conditions, even though it had evolved very hypsodont cheek teeth by about 10 Ma (C. occidentale, s.s.; C. skinneri, n.sp.). Cormohipparion johnsoni, n.sp., and C. merriami, n.sp., are followed by C. fricki, n.sp., at about 12-11.5 Ma, which demonstrates an increased crown height and complexity of the upper cheek teeth along with the persistence of a functional dP1 into the adult condition. At least in C. fricki, n.sp., and likely also C. merriami, n.sp., the pre- and postfossettes of P2 commonly were confluent. All of these features are to be found in early Pannonian C members of Hippotherium of the Old World, and it is likely that a taxon such as C. fricki, n.sp., was associated with the Old World dispersal event that resulted in the presence of H. primigenium. A specimen of Cormohipparion sp. from deposits about 12 Ma old in California shows the proper morphology (enhanced by a significant increase in fossette complexity) to be a possible member of the dispersal population prior to its exit to the Old World at about 11 Ma. Subsequent North American species of the Cormohipparion occidentale group lived from about 11 Ma to 10 Ma and convergently approach (but do not equal) the enamel pattern complexity found in Hippotherium primigenium but surpass it in upper cheek tooth crown height, in the almost complete loss of dP1, and in a diminished frequency of confluence of the pre- and postfossetttes in P2. Two of these species, C. occidentale, s.s., and C. skinneri, n.sp., apparently populated a more northern (Great Plains) versus a southern (Texan) district, with C. occidentale, s.s., being sympatric with the (?secondarily) smaller C. matthewi, n.sp. The sample of C. occidentale, s.s., from the XMas-Kat quarries of Nebraska differs somewhat in a few cranial and dental parameters from samples from the Machaerodus and Hans Johnson quarries. Whereas the material from the XMas-Kat and Machaerodus quarries seems contemporaneous on geological grounds, the age of the sample from the Hans Johnson Quarry is not as securely dated. It is possible that the cranial differences (mainly the size of the preorbital fossa) and dental parameters (the persistence of a small and apparently functionally insignificant dP1 in adult female, but not male, crania) are variations in a contemporaneous but somewhat polymorphic population. Alternatively, it is possible that the Hans Johnson sample, at least, may be chronologically somewhat older than that from the Xmas-Kat quarries and that the morphological differences represent in part a more plesiomorphic condition for its specimens.
138 p. : ill., map ; 26 cm.
Includes bibliographical references (p. 134-138).
Includes bibliographical references (p. 134-138).