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Mexican Pliocene cervids are very poorly known. We report on new fossil material of the roe deer Capreolus constantini recovered from the Pliocene Atotonilco El Grande Formation of Santa Maria Amajac, Hidalgo (central Mexico). The specimens were collected from a series of layers of friable to moderately indurated polymictic conglomerate supported by a sandstone-tuffaceous-calcareous matrix. This species was formerly known only from the late Pliocene of Udunga, Russia, thus implying a dispersal event to North America around 4.0 Ma. This cervid is one of the very small number of mammals recorded from the poorly sampled Pliocene temperate deposits of Mexico.
The backward chewing stroke in multituberculates (unique for mammals) resulted in a more anterior insertion of the masticatory muscles than in any other mammal group, including rodents. Multituberculates differ from tritylodontids in details of the masticatory musculature, but share with them the backward masticatory power stroke and retractory horizontal components of the resultant force of all the masticatory muscles (protractory in Theria). The Taeniolabididae differ from the Eucosmodontidae in having a more powerful masticatory musculature, expressed by the higher zygomatic arch with relatively larger anterior and middle zygomaticridges and higher coronoid process. It is speculated that the bicuspid, or pointed upper incisors, and semi-procumbent, pointed lower ones, characteristic of nontaeniolabidoid multitliberculates were used for picking-up and killing insects or other prey. In relation to the backward power stroke the low position of the condylar process was advantageous for most multituberculates. In extreme cases (Sloanbaataridae and Taeniolabididae), the adaptation for crushing hard seeds, worked against the benefit of the low position of the condylar process and a high condylar process developed. Five new multituberculate autapomorphies are recognized: anterior and intermediate zygomatic ridges: glenoid fossa large, flat and sloping backwards (forwards in rodents), arranged anterolateral and standing out from the braincase; semicircular posterior margin of the dentary with condylar process forming at least a part of it; anterior position of the coronoid process; and anterior position of the masseteric fossa. The postorbital process in those multituberculates studied is situated on the parietal and the orbit is very large.
Systematics of fossil octodontoids (Rodentia, Caviomorpha) is in great part based on insights into the knowledge of teeth, making the step of dental characterization certainly relevant for the evolutionary reconstruction of these rodents. Different homology hypotheses were proposed for the same tooth structures, a fact that indicates the importance of knowing on which criteria the dental characters supporting the classifications were based. In this line, I evaluate the step of characterization of certain conflictive molar characters previously used, and their impact on phylogeny of octodontoids. I explore which the criteria followed to propose the hypotheses of correspondences for these characters are in light of the anatomical evidence. Based on the outcome of phylogenetic trees obtained previously, I analyze if the evolutionary transformations are compatible with character states observed in the terminals. New cladistic analyses based on recoded molar characters indicate that, unlike results recently obtained, the unorthodox position of Sallamys, Protadelphomys, and Willidewu as basal ctenomyines is not recovered. The position of Caviocricetus, Acarechimys–Neophanomysas as Octodontinae is not maintained. These results indicate that reanalyses of conflictive dental characters, scrutinizing data matrices, are particularly necessary to evaluate the current controversy on the phylogeny of octodontoids. Lower molar character definition and character states delimitation in octodontoids, being relevant to phylogenetic reconstruction, should be founded on anatomical examination, following explicit criteria of homology. Alternative hypotheses of “primary homology” proposed for the same molar traits in octodontoids indicate that each main group of caviomorphs requires its own anatomical study.
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