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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...

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Autores principales: Hopwood, Paul E., Head, Megan L., Jordan, Eleanor J., Carter, Mauricio J., Davey, Emma, Moore, Allen J., Royle, Nick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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
title_full Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
title_fullStr Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
title_full_unstemmed Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
title_short Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides
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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