Abstract

The incongruence of character states with phylogenetic relationships is often interpreted as evidence of convergent evolution. However, trait evolution along discordant gene trees can also generate these incongruences - a phenomenon known as hemiplasy. Classic comparative methods do not account for discordance, resulting in incorrect inferences about the number, timing, and direction of trait transitions. Biological sources of discordance include incomplete lineage sorting (ILS) and introgression, but only ILS has received theoretical consideration in the context of hemiplasy. Here, we present a model that shows introgression makes hemiplasy more likely, such that methods that account for ILS alone will be conservative. We also present a method and software (HeIST) for making statistical inferences about the probability of hemiplasy and homoplasy in large datasets that contain both ILS and introgression. We apply our methods to two empirical datasets, finding that hemiplasy is likely to contribute to the observed trait incongruences in both.

Highlights

  • Convergent evolution of the same phenotype in distantly related species provides some of the most compelling evidence for natural selection

  • We define the total probability of a locus following an introgressed history as d, with d2 denoting the probability of C ! B introgression, and d3 the probability of B ! C introgression

  • Introgression makes hemiplasy more likely than incomplete lineage sorting alone Using our model for the probability of hemiplasy and of homoplasy, we examined the ratio Pe/Po over a range of different introgression scenarios

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Summary

Introduction

Convergent evolution of the same phenotype in distantly related species provides some of the most compelling evidence for natural selection. The classic multispecies coalescent model has been extended to include introgression (a term we use to encompass hybridization and subsequent gene flow), in a framework called the ‘multispecies network coalescent’ (Yu et al, 2012; Yu et al, 2014; Wen et al, 2016). In this model, species relationships are modeled as a network, with introgression represented by horizontal reticulation edges.

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