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Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees
A number of methods have been developed to infer differential rates of species diversification through time and among clades using time-calibrated phylogenetic trees. However, we lack a general framework that can delineate and quantify heterogeneous mixtures of dynamic processes within single phylog...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935878/ https://www.ncbi.nlm.nih.gov/pubmed/24586858 http://dx.doi.org/10.1371/journal.pone.0089543 |
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author | Rabosky, Daniel L. |
author_facet | Rabosky, Daniel L. |
author_sort | Rabosky, Daniel L. |
collection | PubMed |
description | A number of methods have been developed to infer differential rates of species diversification through time and among clades using time-calibrated phylogenetic trees. However, we lack a general framework that can delineate and quantify heterogeneous mixtures of dynamic processes within single phylogenies. I developed a method that can identify arbitrary numbers of time-varying diversification processes on phylogenies without specifying their locations in advance. The method uses reversible-jump Markov Chain Monte Carlo to move between model subspaces that vary in the number of distinct diversification regimes. The model assumes that changes in evolutionary regimes occur across the branches of phylogenetic trees under a compound Poisson process and explicitly accounts for rate variation through time and among lineages. Using simulated datasets, I demonstrate that the method can be used to quantify complex mixtures of time-dependent, diversity-dependent, and constant-rate diversification processes. I compared the performance of the method to the MEDUSA model of rate variation among lineages. As an empirical example, I analyzed the history of speciation and extinction during the radiation of modern whales. The method described here will greatly facilitate the exploration of macroevolutionary dynamics across large phylogenetic trees, which may have been shaped by heterogeneous mixtures of distinct evolutionary processes. |
format | Online Article Text |
id | pubmed-3935878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39358782014-03-04 Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees Rabosky, Daniel L. PLoS One Research Article A number of methods have been developed to infer differential rates of species diversification through time and among clades using time-calibrated phylogenetic trees. However, we lack a general framework that can delineate and quantify heterogeneous mixtures of dynamic processes within single phylogenies. I developed a method that can identify arbitrary numbers of time-varying diversification processes on phylogenies without specifying their locations in advance. The method uses reversible-jump Markov Chain Monte Carlo to move between model subspaces that vary in the number of distinct diversification regimes. The model assumes that changes in evolutionary regimes occur across the branches of phylogenetic trees under a compound Poisson process and explicitly accounts for rate variation through time and among lineages. Using simulated datasets, I demonstrate that the method can be used to quantify complex mixtures of time-dependent, diversity-dependent, and constant-rate diversification processes. I compared the performance of the method to the MEDUSA model of rate variation among lineages. As an empirical example, I analyzed the history of speciation and extinction during the radiation of modern whales. The method described here will greatly facilitate the exploration of macroevolutionary dynamics across large phylogenetic trees, which may have been shaped by heterogeneous mixtures of distinct evolutionary processes. Public Library of Science 2014-02-26 /pmc/articles/PMC3935878/ /pubmed/24586858 http://dx.doi.org/10.1371/journal.pone.0089543 Text en © 2014 Daniel L http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rabosky, Daniel L. Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees |
title | Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees |
title_full | Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees |
title_fullStr | Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees |
title_full_unstemmed | Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees |
title_short | Automatic Detection of Key Innovations, Rate Shifts, and Diversity-Dependence on Phylogenetic Trees |
title_sort | automatic detection of key innovations, rate shifts, and diversity-dependence on phylogenetic trees |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935878/ https://www.ncbi.nlm.nih.gov/pubmed/24586858 http://dx.doi.org/10.1371/journal.pone.0089543 |
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