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Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait
Theory shows how sexual selection can exaggerate male traits beyond naturally selected optima and also how natural selection can ultimately halt trait elaboration. Empirical evidence supports this theory, but to our knowledge, there have been no experimental evolution studies directly testing this l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187464/ https://www.ncbi.nlm.nih.gov/pubmed/34103535 http://dx.doi.org/10.1038/s41467-021-23804-7 |
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author | Okada, Kensuke Katsuki, Masako Sharma, Manmohan D. Kiyose, Katsuya Seko, Tomokazu Okada, Yasukazu Wilson, Alastair J. Hosken, David J. |
author_facet | Okada, Kensuke Katsuki, Masako Sharma, Manmohan D. Kiyose, Katsuya Seko, Tomokazu Okada, Yasukazu Wilson, Alastair J. Hosken, David J. |
author_sort | Okada, Kensuke |
collection | PubMed |
description | Theory shows how sexual selection can exaggerate male traits beyond naturally selected optima and also how natural selection can ultimately halt trait elaboration. Empirical evidence supports this theory, but to our knowledge, there have been no experimental evolution studies directly testing this logic, and little examination of possible associated effects on female fitness. Here we use experimental evolution of replicate populations of broad-horned flour beetles to test for effects of sex-specific predation on an exaggerated sexually selected male trait (the mandibles), while also testing for effects on female lifetime reproductive success. We find that populations subjected to male-specific predation evolve smaller sexually selected mandibles and this indirectly increases female fitness, seemingly through intersexual genetic correlations we document. Predation solely on females has no effects. Our findings support fundamental theory, but also reveal unforseen outcomes—the indirect effect on females—when natural selection targets sex-limited sexually selected characters. |
format | Online Article Text |
id | pubmed-8187464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81874642021-07-01 Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait Okada, Kensuke Katsuki, Masako Sharma, Manmohan D. Kiyose, Katsuya Seko, Tomokazu Okada, Yasukazu Wilson, Alastair J. Hosken, David J. Nat Commun Article Theory shows how sexual selection can exaggerate male traits beyond naturally selected optima and also how natural selection can ultimately halt trait elaboration. Empirical evidence supports this theory, but to our knowledge, there have been no experimental evolution studies directly testing this logic, and little examination of possible associated effects on female fitness. Here we use experimental evolution of replicate populations of broad-horned flour beetles to test for effects of sex-specific predation on an exaggerated sexually selected male trait (the mandibles), while also testing for effects on female lifetime reproductive success. We find that populations subjected to male-specific predation evolve smaller sexually selected mandibles and this indirectly increases female fitness, seemingly through intersexual genetic correlations we document. Predation solely on females has no effects. Our findings support fundamental theory, but also reveal unforseen outcomes—the indirect effect on females—when natural selection targets sex-limited sexually selected characters. Nature Publishing Group UK 2021-06-08 /pmc/articles/PMC8187464/ /pubmed/34103535 http://dx.doi.org/10.1038/s41467-021-23804-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Okada, Kensuke Katsuki, Masako Sharma, Manmohan D. Kiyose, Katsuya Seko, Tomokazu Okada, Yasukazu Wilson, Alastair J. Hosken, David J. Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
title | Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
title_full | Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
title_fullStr | Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
title_full_unstemmed | Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
title_short | Natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
title_sort | natural selection increases female fitness by reversing the exaggeration of a male sexually selected trait |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187464/ https://www.ncbi.nlm.nih.gov/pubmed/34103535 http://dx.doi.org/10.1038/s41467-021-23804-7 |
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