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Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
Male and female genital morphology varies widely across many taxa, and even among populations. Disentangling potential sources of selection on genital morphology is problematic because each sex is predicted to respond to adaptations in the other due to reproductive conflicts of interest. To test how...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089618/ https://www.ncbi.nlm.nih.gov/pubmed/27144373 http://dx.doi.org/10.1111/evo.12938 |
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author | Hopwood, Paul E. Head, Megan L. Jordan, Eleanor J. Carter, Mauricio J. Davey, Emma Moore, Allen J. Royle, Nick J. |
author_facet | Hopwood, Paul E. Head, Megan L. Jordan, Eleanor J. Carter, Mauricio J. Davey, Emma Moore, Allen J. Royle, Nick J. |
author_sort | Hopwood, Paul E. |
collection | PubMed |
description | Male and female genital morphology varies widely across many taxa, and even among populations. Disentangling potential sources of selection on genital morphology is problematic because each sex is predicted to respond to adaptations in the other due to reproductive conflicts of interest. To test how variation in this sexual conflict trait relates to variation in genital morphology we used our previously developed artificial selection lines for high and low repeated mating rates. We selected for high and low repeated mating rates using monogamous pairings to eliminate contemporaneous female choice and male–male competition. Male and female genital shape responded rapidly to selection on repeated mating rate. High and low mating rate lines diverged from control lines after only 10 generations of selection. We also detected significant patterns of male and female genital shape coevolution among selection regimes. We argue that because our selection lines differ in sexual conflict, these results support the hypothesis that sexually antagonistic coevolution can drive the rapid divergence of genital morphology. The greatest divergence in morphology corresponded with lines in which the resolution of sexual conflict over mating rate was biased in favor of male interests. |
format | Online Article Text |
id | pubmed-5089618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50896182016-11-09 Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides Hopwood, Paul E. Head, Megan L. Jordan, Eleanor J. Carter, Mauricio J. Davey, Emma Moore, Allen J. Royle, Nick J. Evolution Original Articles Male and female genital morphology varies widely across many taxa, and even among populations. Disentangling potential sources of selection on genital morphology is problematic because each sex is predicted to respond to adaptations in the other due to reproductive conflicts of interest. To test how variation in this sexual conflict trait relates to variation in genital morphology we used our previously developed artificial selection lines for high and low repeated mating rates. We selected for high and low repeated mating rates using monogamous pairings to eliminate contemporaneous female choice and male–male competition. Male and female genital shape responded rapidly to selection on repeated mating rate. High and low mating rate lines diverged from control lines after only 10 generations of selection. We also detected significant patterns of male and female genital shape coevolution among selection regimes. We argue that because our selection lines differ in sexual conflict, these results support the hypothesis that sexually antagonistic coevolution can drive the rapid divergence of genital morphology. The greatest divergence in morphology corresponded with lines in which the resolution of sexual conflict over mating rate was biased in favor of male interests. John Wiley and Sons Inc. 2016-05-24 2016-06 /pmc/articles/PMC5089618/ /pubmed/27144373 http://dx.doi.org/10.1111/evo.12938 Text en © 2016 The Author(s). Evolution published by Wiley Periodicals, Inc. on behalf of The Society for the Study of Evolution. This is an open access article under the terms of the Creative Commons (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hopwood, Paul E. Head, Megan L. Jordan, Eleanor J. Carter, Mauricio J. Davey, Emma Moore, Allen J. Royle, Nick J. Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides |
title | Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
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title_full | Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
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title_fullStr | Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
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title_full_unstemmed | Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
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title_short | Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
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title_sort | selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, nicrophorus vespilloides |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089618/ https://www.ncbi.nlm.nih.gov/pubmed/27144373 http://dx.doi.org/10.1111/evo.12938 |
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