Metapopulation structure modulates sexual antagonism

Abstract 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 insec...

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Main Authors: E. Rodriguez‐Exposito, F. Garcia‐Gonzalez
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:Evolution Letters
Subjects:
Online Access:https://doi.org/10.1002/evl3.244
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spelling doaj-b77f4262318f48dcb232de7fb5be1d402021-08-02T14:22:29ZengWileyEvolution Letters2056-37442021-08-015434435810.1002/evl3.244Metapopulation structure modulates sexual antagonismE. Rodriguez‐Exposito0F. Garcia‐Gonzalez1Doñana Biological Station (EBD‐CSIC) Isla de la Cartuja Sevilla SpainDoñana Biological Station (EBD‐CSIC) Isla de la Cartuja Sevilla SpainAbstract 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.https://doi.org/10.1002/evl3.244Callosobruchus maculatusecological contextevolutionary ecologyexperimental evolutionfemale resistance to male harmmetapopulation structure
collection DOAJ
language English
format Article
sources DOAJ
author E. Rodriguez‐Exposito
F. Garcia‐Gonzalez
spellingShingle E. Rodriguez‐Exposito
F. Garcia‐Gonzalez
Metapopulation structure modulates sexual antagonism
Evolution Letters
Callosobruchus maculatus
ecological context
evolutionary ecology
experimental evolution
female resistance to male harm
metapopulation structure
author_facet E. Rodriguez‐Exposito
F. Garcia‐Gonzalez
author_sort E. Rodriguez‐Exposito
title Metapopulation structure modulates sexual antagonism
title_short 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_sort metapopulation structure modulates sexual antagonism
publisher Wiley
series Evolution Letters
issn 2056-3744
publishDate 2021-08-01
description Abstract 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.
topic Callosobruchus maculatus
ecological context
evolutionary ecology
experimental evolution
female resistance to male harm
metapopulation structure
url https://doi.org/10.1002/evl3.244
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AT fgarciagonzalez metapopulationstructuremodulatessexualantagonism
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