Abstract

BackgroundThe vast majority of all life that ever existed on earth is now extinct and several aspects of their evolutionary history can only be assessed by using morphological data from the fossil record. Sphenodontian reptiles are a classic example, having an evolutionary history of at least 230 million years, but currently represented by a single living species (Sphenodon punctatus). Hence, it is imperative to improve the development and implementation of probabilistic models to estimate evolutionary trees from morphological data (e.g., morphological clocks), which has direct benefits to understanding relationships and evolutionary patterns for both fossil and living species. However, the impact of model choice on morphology-only datasets has been poorly explored.ResultsHere, we investigate the impact of a wide array of model choices on the inference of evolutionary trees and macroevolutionary parameters (divergence times and evolutionary rates) using a new data matrix on sphenodontian reptiles. Specifically, we tested different clock models, clock partitioning, taxon sampling strategies, sampling for ancestors, and variations on the fossilized birth-death (FBD) tree model parameters through time. We find a strong impact on divergence times and background evolutionary rates when applying widely utilized approaches, such as allowing for ancestors in the tree and the inappropriate assumption of diversification parameters being constant through time. We compare those results with previous studies on the impact of model choice to molecular data analysis and provide suggestions for improving the implementation of morphological clocks. Optimal model combinations find the radiation of most major lineages of sphenodontians to be in the Triassic and a gradual but continuous drop in morphological rates of evolution across distinct regions of the phenotype throughout the history of the group.ConclusionsWe provide a new hypothesis of sphenodontian classification, along with detailed macroevolutionary patterns in the evolutionary history of the group. Importantly, we provide suggestions to avoid overestimated divergence times and biased parameter estimates using morphological clocks. Partitioning relaxed clocks offers methodological limitations, but those can be at least partially circumvented to reveal a detailed assessment of rates of evolution across the phenotype and tests of evolutionary mosaicism.

Highlights

  • The vast majority of all life that ever existed on earth is extinct and several aspects of their evolutionary history can only be assessed by using morphological data from the fossil record

  • Results obtained under the fossilized birth-death (FBD) and the skyline FBD (SFBD) tree model with distinct taxon sampling strategies and relaxed clock models

  • Results obtained under the FBD and SFBD tree models with a NoSA diversity taxon sampling strategy and the autocorrelated relaxed clock model

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Summary

Introduction

The vast majority of all life that ever existed on earth is extinct and several aspects of their evolutionary history can only be assessed by using morphological data from the fossil record. It is imperative to improve the development and implementation of probabilistic models to estimate evolutionary trees from morphological data (e.g., morphological clocks), which has direct benefits to understanding relationships and evolutionary patterns for both fossil and living species. Morphological characters and fossil data (both specimens and their ages) contribute to improved divergence time estimates in total-evidence phylogenies of extant organisms [2, 3], providing a more holistic reconstruction of the tree of life. It constitutes the sole source of data to investigate the phylogeny and macroevolution of most extinct lineages. Morphological clocks have been used to estimate divergence times for entirely extinct lineages [e.g., [8,9,10]], or in combination with molecular data (“morpho-molecular clocks” in total-evidence dating) to estimate evolutionary trees and divergence times for clades with extant representatives [e.g., [11,12,13,14,15]]

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