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Chatterji, R. M.

Publications and source records attributed to Chatterji, R. M..

2 recordsLinked to original sources

Geometric morphometrics enables accurate predictions of paleoecology and reveals unique adaptations to an expanded niche space in extinct waterfowl

Establishing the relationships between organismal phenotypes and their environment is a key component to understanding evolutionary history. Comparative evaluations of extant and extinct species can reveal how lineages have adapted to changing environmental conditions over time. However, the understanding of paleoecologies is predicated on a robust understanding of how modern species have been shaped by adaptation. Waterfowl may present an ideal group to study adaptive evolution as much of their morphology is apparently shaped by their dietary ecology. Here we use a large geometric morphometric dataset of waterfowl combined with random forest, a supervised machine learning algorithm, and linear discriminate analysis, to predict the dietary ecologies of nine extinct waterfowl species. We find that both model types reliably predict ecology for extinct species with well-established diets. Interestingly, we also found that the Hawaiian moa-nalo and the New Zealand Cnemiornis calcitrans likely occupied ecological niches no longer present in modern waterfowl as they were not morphologically or ecologically convergent with modern geese as previously asserted. Our study demonstrates that waterfowl are an excellent model group for the study of adaptive evolution, and underscores the utility of predictive modelling for paleontological studies.

evolutionary biology↗

Dietary specialization drives adaptation, convergence, and integration across the cranial and appendicular skeleton in Waterfowl (Anseriformes).

Convergence provides strong evidence for adaptive evolution as it reflects shared adaptive responses to the same selection pressures. The waterfowl (order Anseriformes) are an ideal group in which to study convergent evolution as they have repeatedly evolved morphotypes putatively correlated with diet (i.e., dabbler, grazer, diver). Here, we construct the most robust evolutionary hypothesis to date for waterfowl and reveal widespread morphological convergence across the order. We quantified the shape of the skull and hindlimb elements (femur, tibiotarsus, and tarsometatarsus) of 118 species of extant waterfowl using geometric morphometrics. Multivariate generalized evolutionary models provide strong support for a relationship between dietary ecology and skull shape, and evidence for convergent evolution across lineages that share dietary niches. Foraging behavior better explained the evolution of hindlimb shape, but diet still contributed significantly. We also find preliminary evidence for integration across all three measured hindlimb elements with each other and with the skull. We demonstrate that dietary ecology drives morphological convergence within waterfowl, that this convergent evolution involves multiple integrated skeletal structures, and that morphological changes are associated with shifts in the rate of phenotypic evolution.

evolutionary biology↗