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Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display
Female mating preferences for exaggerated male display traits are commonplace. Yet, comprehensive understanding of the evolution and persistence of costly female preference through indirect (Fisherian) selection in finite populations requires some explanation for the persistence of additive genetic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302702/ https://www.ncbi.nlm.nih.gov/pubmed/34964487 http://dx.doi.org/10.1111/evo.14426 |
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author | Tschol, Maximilian Reid, Jane M. Bocedi, Greta |
author_facet | Tschol, Maximilian Reid, Jane M. Bocedi, Greta |
author_sort | Tschol, Maximilian |
collection | PubMed |
description | Female mating preferences for exaggerated male display traits are commonplace. Yet, comprehensive understanding of the evolution and persistence of costly female preference through indirect (Fisherian) selection in finite populations requires some explanation for the persistence of additive genetic variance (V (a)) underlying sexual traits, given that directional preference is expected to deplete V (a) in display and hence halt preference evolution. However, the degree to which V (a), and hence preference‐display coevolution, may be prolonged by spatially variable sexual selection arising solely from limited gene flow and genetic drift within spatially structured populations has not been examined. Our genetically and spatially explicit model shows that spatial population structure arising in an ecologically homogeneous environment can facilitate evolution and long‐term persistence of costly preference given small subpopulations and low dispersal probabilities. Here, genetic drift initially creates spatial variation in female preference, leading to persistence of V (a) in display through “migration‐bias” of genotypes maladapted to emerging local sexual selection, thus fueling coevolution of costly preference and display. However, costs of sexual selection increased the probability of subpopulation extinction, limiting persistence of high preference‐display genotypes. Understanding long‐term dynamics of sexual selection systems therefore requires joint consideration of coevolution of sexual traits and metapopulation dynamics. |
format | Online Article Text |
id | pubmed-9302702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93027022022-07-22 Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display Tschol, Maximilian Reid, Jane M. Bocedi, Greta Evolution Brief Communications Female mating preferences for exaggerated male display traits are commonplace. Yet, comprehensive understanding of the evolution and persistence of costly female preference through indirect (Fisherian) selection in finite populations requires some explanation for the persistence of additive genetic variance (V (a)) underlying sexual traits, given that directional preference is expected to deplete V (a) in display and hence halt preference evolution. However, the degree to which V (a), and hence preference‐display coevolution, may be prolonged by spatially variable sexual selection arising solely from limited gene flow and genetic drift within spatially structured populations has not been examined. Our genetically and spatially explicit model shows that spatial population structure arising in an ecologically homogeneous environment can facilitate evolution and long‐term persistence of costly preference given small subpopulations and low dispersal probabilities. Here, genetic drift initially creates spatial variation in female preference, leading to persistence of V (a) in display through “migration‐bias” of genotypes maladapted to emerging local sexual selection, thus fueling coevolution of costly preference and display. However, costs of sexual selection increased the probability of subpopulation extinction, limiting persistence of high preference‐display genotypes. Understanding long‐term dynamics of sexual selection systems therefore requires joint consideration of coevolution of sexual traits and metapopulation dynamics. John Wiley and Sons Inc. 2022-01-19 2022-03 /pmc/articles/PMC9302702/ /pubmed/34964487 http://dx.doi.org/10.1111/evo.14426 Text en © 2021 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Brief Communications Tschol, Maximilian Reid, Jane M. Bocedi, Greta Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
title | Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
title_full | Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
title_fullStr | Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
title_full_unstemmed | Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
title_short | Strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
title_sort | strong spatial population structure shapes the temporal coevolutionary dynamics of costly female preference and male display |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302702/ https://www.ncbi.nlm.nih.gov/pubmed/34964487 http://dx.doi.org/10.1111/evo.14426 |
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