Rise of present-day tetrapods in the paleotropics of Late Triassic equatorial Pangaea: new insights from microvertebrate data

The Triassic Period (~252–201.5 Ma) saw a transformative radiation and reorganization of continental tetrapod diversity following the end-Permian Extinction, including an assemblage of diverse forms that do not survive the end-Triassic (herein termed the 'endemic Triassic fauna', =ETF), as well as the earliest fossil representatives of all major modern tetrapod groups (herein termed the 'Living [Triassic to Recent] Fauna', =LTF; i.e. Salientia, Caudata, Gymnophiona, Mammaliaformes, Squamata, Rhynchocephalia, Testudinata, Crocodylomorpha, and Dinosauria). With few exceptions, only the LTF assemblage survives the end-Triassic Extinction (~201.5 Ma), highlighting the Late Triassic (~227–201.5 Ma) record as essential for understanding this pivotal transition and the evolutionary and ecological origins of post-Triassic non-marine tetrapod faunas, including those of present day. Micro-microvertebrate bonebeds are arguably the best proxy for tracking continental vertebrate biodiversity, however gaps in their Late Triassic record obscure patterns and drivers of evolutionary, ecological, and environmental change during the rise of LTF communities. In my dissertation, I use new data collected from Upper Triassic microvertebrate bonebeds from North America, and particularly the Thunderstorm Ridge site (PFV 456) in Petrified Forest National Park, Arizona, U.S.A, to fill gaps in the evolutionary record of specific groups (e.g., lissamphibians and lepidosaurs), as well as the vertebrate paleocommunity record of Triassic equatorial Pangaea. My first chapter describes and analyzes an assemblage of gymnophionomorph (stem caecilian) bones from PFV 456 which represent the oldest-known caecilian fossils globally. As the oldest caecilian fossils, they provide new support for the dissorophoid temnospondyl affinities of caecilians and other living amphibians, evidence of a step-wise acquisition of caecilian anatomies associated with fossoriality, and evidence of an ancient pattern of equatorial biogeographic restriction in caecilians from the Triassic to the present day. My second chapter describes and analyzes an assemblage of lepidosauromorphs from the Late Triassic of Equatorial Pangaea, providing new insights into the step-wise evolution tooth and jaw morphologies near the divergence of living lepidosaur clades (Squamata and Rhynchocephalia), and showing evidence for the Triassic acquisition in stem squamates and non-squamate lepidosaurs of dental features conserved in living squamates. The third chapter uses apomorphy-based identifications to describe the vertebrate diversity of the Thunderstorm Ridge site (PFV 456), providing evidence for the most species rich continental vertebrate community yet-known from the Triassic, with 55 vertebrate taxa. Nearly all LTF clades are present, predating similar assemblages from the early Jurassic by over 20 million years, and indicating that the assembly of the first LTF communities by at least 220 million years ago, long before the Triassic-Jurassic Extinction event (~201.5). The presence of this exceptional diversity may be linked to the climatic and environmental settings of equatorial Pangaea during the Triassic.