Abstract
In a previous study, we estimated the cranial disparity of turtles (Testudinata) through time using geometric morphometric data from both terminal taxa and hypothetical ancestors to compensate for temporal gaps in the fossil record. While this method yielded reasonable results for the Mesozoic and the early Cenozoic, we found a large drop in cranial disparity for the Miocene, for which we found no correlation with known environmental changes or extinction events. Instead, we speculated that the Miocene dip was a result of poor sampling of fossils or ancestors in this time bin. To countervail this problem, we here updated our original dataset and interpolated changes of shape along the branch lengths and compared them with the previous data. We furthermore explored the impact of topological and temporal uncertainty, demonstrating that the Miocene dip, indeed, is a sampling artefact. All remaining conclusions of the previous study could be more or less supported, nevertheless, including an apparent correlation with global biogeographic events, a minor correlation between cranial disparity and global temperature, and resilience across the K/T extinction event.
Highlights
Over the course of the last decades, the combination of geometric morphometrics with phylogenetic comparative methods has become a promising resource for the study of macroevolutionary dynamics, including the evolution of disparity, which quantifies morphological diversity as opposed to taxonomic, functional or phylogenetic diversity [1,2,3,4,5]
As in the original analyses, only a minor perturbation is apparent at the K/T extinction event, but the peak of cranial disparity is much lessened, and shifted from early Eocene to the Maastrichtian
In contrast to our initial analysis, our revised analysis reveals that turtles maintained a high level of disparity in skull shape throughout the Cenozoic, instead of showing a strong decline towards the Miocene, followed by a recovery towards the Recent
Summary
Over the course of the last decades, the combination of geometric morphometrics with phylogenetic comparative methods has become a promising resource for the study of macroevolutionary dynamics, including the evolution of disparity, which quantifies morphological diversity as opposed to taxonomic, functional or phylogenetic diversity [1,2,3,4,5].
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