Fossoriality evolved early in snakes, and has left its signature on the cranial morphology of many extinct Mesozoic and early Caenozoic forms. Knowledge of the cranial osteology of extant snakes is indispensable for associating the crania of extinct lineages with a particular mode of life; this applies to fossorial taxa as well. In the present work, we provide a detailed description of the cranium of Hypoptophis wilsonii, a member of the subfamily Aparallactinae, using micro-computed tomography (CT). This is also the first thorough micro-CT-based description of any snake assigned to this African subfamily of predominantly mildly venomous, fossorial, and elusive snakes. The cranium of Hypoptophis is adapted for a fossorial lifestyle, with increased consolidation of skull bones. Aparallactines show a tendency toward reduction of maxillary length by bringing the rear fangs forward. This development attains its pinnacle in the sister subfamily Atractaspidinae, in which the rear fang has become the “front fang” by a loss of the part of the maxilla lying ahead of the fang. These dentitional changes likely reflect adaptation to subdue prey in snug burrows. An endocast of the inner ear of Hypoptophis shows that this genus has the inner ear typical of fossorial snakes, with a large, globular sacculus. A phylogenetic analysis based on morphology recovers Hypoptophis as a sister taxon to Aparallactus. We also discuss the implications of our observations on the burrowing origin hypothesis of snakes.
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RBINS Staff Publications 2022
New remains of the early Eocene hyaenodontid Indohyaenodon raoi are described from the Vastan Lignite Mine in Gujarat, western India, including the first known rostrum, upper dentition, and postcrania, substantially expanding our knowledge of the species and providing insights into its functional morphology and relationships. Craniodental morphology suggests that I. raoi had a broad diet, including non-vertebrate material as well as flesh of a diversity of prey species. Postcranial morphology is broadly similar to that of other early hyaenodontids and suggests a scansorial locomotor repertoire. Dental morphology indicates that I. raoi is closely related to other South Asian hyaenodontids, with shared features including strong cingula, narrow premolars, and a reduced P4 protocone. We present the most comprehensive phylogenetic analysis of Hyaenodontidae to date, which corroborates this relationship but finds South Asian hyaenodontids to be the stem of a group that includes most African hyaenodontids. This and other higher-level relationships within Hyaenodontidae are, however, weakly supported, and substantially different alternative hypotheses of relationships are not significantly less parsimonious, reflecting strong character conflict. Factors contributing to this conflict include the isolation of hyaenodontid faunas on different continents during much of the Eocene, canalization and simplification of carnivorous dentitions, and a lack of non-dental material for critical hyaenodontid groups. The new phylogeny is consistent with either an African or an Asian origin for the group.
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