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Metapopulation structure modulates sexual antagonism
Despite the far‐reaching evolutionary implications of sexual conflict, the effects of metapopulation structure, when populations are subdivided into several demes connected to some degree by migration, on sexual conflict dynamics are unknown. Here, we used experimental evolution in an insect model s...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327942/ https://www.ncbi.nlm.nih.gov/pubmed/34367660 http://dx.doi.org/10.1002/evl3.244 |
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author | Rodriguez‐Exposito, E. Garcia‐Gonzalez, F. |
author_facet | Rodriguez‐Exposito, E. Garcia‐Gonzalez, F. |
author_sort | Rodriguez‐Exposito, E. |
collection | PubMed |
description | Despite the far‐reaching evolutionary implications of sexual conflict, the effects of metapopulation structure, when populations are subdivided into several demes connected to some degree by migration, on sexual conflict dynamics are unknown. Here, we used experimental evolution in an insect model system, the seed beetle Callosobruchus maculatus, to assess the independent and interacting effects of selection histories associated with mating system (monogamy vs. polygamy) and population subdivision on sexual conflict evolution. We confirm traditional predictions from sexual conflict theory by revealing increased resistance to male harm in females from populations with a history of intense sexual selection (polygamous populations) compared to females from populations with a history of relaxed sexual selection (monogamous populations). However, selection arising from metapopulation structure reversed the classic pattern of sexually antagonistic coevolution and led to reduced resistance in females from polygamous populations. These results underscore that population spatial structure moderates sexual selection and sexual conflict, and more broadly, that the evolution of sexual conflict is contingent on ecological context. The findings also have implications for population dynamics, conservation biology, and biological control. |
format | Online Article Text |
id | pubmed-8327942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83279422021-08-06 Metapopulation structure modulates sexual antagonism Rodriguez‐Exposito, E. Garcia‐Gonzalez, F. Evol Lett Letters Despite the far‐reaching evolutionary implications of sexual conflict, the effects of metapopulation structure, when populations are subdivided into several demes connected to some degree by migration, on sexual conflict dynamics are unknown. Here, we used experimental evolution in an insect model system, the seed beetle Callosobruchus maculatus, to assess the independent and interacting effects of selection histories associated with mating system (monogamy vs. polygamy) and population subdivision on sexual conflict evolution. We confirm traditional predictions from sexual conflict theory by revealing increased resistance to male harm in females from populations with a history of intense sexual selection (polygamous populations) compared to females from populations with a history of relaxed sexual selection (monogamous populations). However, selection arising from metapopulation structure reversed the classic pattern of sexually antagonistic coevolution and led to reduced resistance in females from polygamous populations. These results underscore that population spatial structure moderates sexual selection and sexual conflict, and more broadly, that the evolution of sexual conflict is contingent on ecological context. The findings also have implications for population dynamics, conservation biology, and biological control. John Wiley and Sons Inc. 2021-06-30 /pmc/articles/PMC8327942/ /pubmed/34367660 http://dx.doi.org/10.1002/evl3.244 Text en © 2021 The Authors. Evolution Letters published by Wiley Periodicals LLC on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters Rodriguez‐Exposito, E. Garcia‐Gonzalez, F. Metapopulation structure modulates sexual antagonism |
title | Metapopulation structure modulates sexual antagonism |
title_full | Metapopulation structure modulates sexual antagonism |
title_fullStr | Metapopulation structure modulates sexual antagonism |
title_full_unstemmed | Metapopulation structure modulates sexual antagonism |
title_short | Metapopulation structure modulates sexual antagonism |
title_sort | metapopulation structure modulates sexual antagonism |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327942/ https://www.ncbi.nlm.nih.gov/pubmed/34367660 http://dx.doi.org/10.1002/evl3.244 |
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