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A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex
Determining the processes responsible for phenotypic variation is one of the central tasks of evolutionary biology. While the importance of acoustic traits for foraging and communication in echolocating mammals suggests adaptation, the seldom-tested null hypothesis to explain trait divergence is gen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460761/ https://www.ncbi.nlm.nih.gov/pubmed/30120366 http://dx.doi.org/10.1038/s41437-018-0129-3 |
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author | Dávalos, Liliana M. Lancaster, Winston C. Núñez-Novas, Miguel S. León, Yolanda M. Lei, Bonnie Flanders, Jon Russell, Amy L. |
author_facet | Dávalos, Liliana M. Lancaster, Winston C. Núñez-Novas, Miguel S. León, Yolanda M. Lei, Bonnie Flanders, Jon Russell, Amy L. |
author_sort | Dávalos, Liliana M. |
collection | PubMed |
description | Determining the processes responsible for phenotypic variation is one of the central tasks of evolutionary biology. While the importance of acoustic traits for foraging and communication in echolocating mammals suggests adaptation, the seldom-tested null hypothesis to explain trait divergence is genetic drift. Here we derive F(ST) values from multi-locus coalescent isolation-with-migration models, and couple them with estimates of quantitative trait divergence, or P(ST), to test drift as the evolutionary process responsible for phenotypic divergence in island populations of the Pteronotus parnellii species complex. Compared to traditional comparisons of P(ST) to F(ST), the migration-based estimates of F(ST) are unidirectional instead of bidirectional, simultaneously integrate variation among loci and individuals, and posterior densities of P(ST) and F(ST) can be compared directly. We found the evolution of higher call frequencies is inconsistent with genetic drift for the Hispaniolan population, despite many generations of isolation from its Puerto Rican counterpart. While the Hispaniolan population displays dimorphism in call frequencies, the higher frequency of the females is incompatible with sexual selection. Instead, cultural drift toward higher frequencies among Hispaniolan females might explain the divergence. By integrating Bayesian coalescent and trait analyses, this study demonstrates a powerful approach to testing genetic drift as the default evolutionary mechanism of trait differentiation between populations. |
format | Online Article Text |
id | pubmed-6460761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-64607612019-10-09 A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex Dávalos, Liliana M. Lancaster, Winston C. Núñez-Novas, Miguel S. León, Yolanda M. Lei, Bonnie Flanders, Jon Russell, Amy L. Heredity (Edinb) Article Determining the processes responsible for phenotypic variation is one of the central tasks of evolutionary biology. While the importance of acoustic traits for foraging and communication in echolocating mammals suggests adaptation, the seldom-tested null hypothesis to explain trait divergence is genetic drift. Here we derive F(ST) values from multi-locus coalescent isolation-with-migration models, and couple them with estimates of quantitative trait divergence, or P(ST), to test drift as the evolutionary process responsible for phenotypic divergence in island populations of the Pteronotus parnellii species complex. Compared to traditional comparisons of P(ST) to F(ST), the migration-based estimates of F(ST) are unidirectional instead of bidirectional, simultaneously integrate variation among loci and individuals, and posterior densities of P(ST) and F(ST) can be compared directly. We found the evolution of higher call frequencies is inconsistent with genetic drift for the Hispaniolan population, despite many generations of isolation from its Puerto Rican counterpart. While the Hispaniolan population displays dimorphism in call frequencies, the higher frequency of the females is incompatible with sexual selection. Instead, cultural drift toward higher frequencies among Hispaniolan females might explain the divergence. By integrating Bayesian coalescent and trait analyses, this study demonstrates a powerful approach to testing genetic drift as the default evolutionary mechanism of trait differentiation between populations. Springer International Publishing 2018-08-17 2019-04 /pmc/articles/PMC6460761/ /pubmed/30120366 http://dx.doi.org/10.1038/s41437-018-0129-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dávalos, Liliana M. Lancaster, Winston C. Núñez-Novas, Miguel S. León, Yolanda M. Lei, Bonnie Flanders, Jon Russell, Amy L. A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
title | A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
title_full | A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
title_fullStr | A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
title_full_unstemmed | A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
title_short | A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
title_sort | coalescent-based estimator of genetic drift, and acoustic divergence in the pteronotus parnellii species complex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460761/ https://www.ncbi.nlm.nih.gov/pubmed/30120366 http://dx.doi.org/10.1038/s41437-018-0129-3 |
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