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Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it?
1. Sexes often differ more obviously in secondary sexual characteristics than in traits that appear naturally selected, despite conceivable benefits to intersexual niche partitioning. Genetic constraints may play a role in limiting sex‐specific niche evolution; however, it is not clear why this limi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453853/ https://www.ncbi.nlm.nih.gov/pubmed/33759459 http://dx.doi.org/10.1111/1365-2656.13487 |
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author | Li, Xiang‐Yi Kokko, Hanna |
author_facet | Li, Xiang‐Yi Kokko, Hanna |
author_sort | Li, Xiang‐Yi |
collection | PubMed |
description | 1. Sexes often differ more obviously in secondary sexual characteristics than in traits that appear naturally selected, despite conceivable benefits to intersexual niche partitioning. Genetic constraints may play a role in limiting sex‐specific niche evolution; however, it is not clear why this limit should apply to naturally selected traits more than those under sexual selection; the latter routinely produces dimorphism. We ask whether ecological factors and/or features of the mating system limit dimorphism in resource use, or conversely, what conditions are the most permissible ones for sexual niche differences. 2. The scale of mating competition and spatial variation in resource availability can help predict sexually dimorphic niches or the lack thereof. We investigate why and when dimorphism might fail to evolve even if genetic covariation between the sexes posed no constraint. 3. Our analytical model incorporates the first aspect of spatial interactions (scale of mating competition). It is followed by simulations that explore broader conditions, including multiple resources with habitat heterogeneity, genetic correlations and non‐Gaussian resource‐use efficiency functions. 4. We recover earlier known conditions for favourable conditions for the evolution of niche partitioning between sexes, such as narrow individual niche and low degrees of genetic constraint. We also show spatial considerations to alter this picture. Sexual niche divergence occurs more readily when local mating groups are small and different resources occur reliably across habitats. Polygyny (medium‐sized or large mating groups) can diminish the prospects for dimorphism even if no genetic constraints are present. Habitat heterogeneity typically also disfavours niche dimorphism but can also lead to polymorphism within a sex, if it is beneficial to specialize to be very competitive in one habitat, even at a cost to performance in the other. 5. Sexual conflict is usually used to explain dimorphic traits or behaviours. Our models highlight that introducing conflict (achieved by switching from monogamy to polygamy) can also be responsible for sexual monomorphism. Under monogamy, males benefit from specializing to consume other resources than what feeds the female best. Polygyny makes males disregard this female benefit, and both sexes compete for the most profitable resource, leading to overlapping niches. |
format | Online Article Text |
id | pubmed-8453853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84538532021-09-27 Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? Li, Xiang‐Yi Kokko, Hanna J Anim Ecol Research Articles 1. Sexes often differ more obviously in secondary sexual characteristics than in traits that appear naturally selected, despite conceivable benefits to intersexual niche partitioning. Genetic constraints may play a role in limiting sex‐specific niche evolution; however, it is not clear why this limit should apply to naturally selected traits more than those under sexual selection; the latter routinely produces dimorphism. We ask whether ecological factors and/or features of the mating system limit dimorphism in resource use, or conversely, what conditions are the most permissible ones for sexual niche differences. 2. The scale of mating competition and spatial variation in resource availability can help predict sexually dimorphic niches or the lack thereof. We investigate why and when dimorphism might fail to evolve even if genetic covariation between the sexes posed no constraint. 3. Our analytical model incorporates the first aspect of spatial interactions (scale of mating competition). It is followed by simulations that explore broader conditions, including multiple resources with habitat heterogeneity, genetic correlations and non‐Gaussian resource‐use efficiency functions. 4. We recover earlier known conditions for favourable conditions for the evolution of niche partitioning between sexes, such as narrow individual niche and low degrees of genetic constraint. We also show spatial considerations to alter this picture. Sexual niche divergence occurs more readily when local mating groups are small and different resources occur reliably across habitats. Polygyny (medium‐sized or large mating groups) can diminish the prospects for dimorphism even if no genetic constraints are present. Habitat heterogeneity typically also disfavours niche dimorphism but can also lead to polymorphism within a sex, if it is beneficial to specialize to be very competitive in one habitat, even at a cost to performance in the other. 5. Sexual conflict is usually used to explain dimorphic traits or behaviours. Our models highlight that introducing conflict (achieved by switching from monogamy to polygamy) can also be responsible for sexual monomorphism. Under monogamy, males benefit from specializing to consume other resources than what feeds the female best. Polygyny makes males disregard this female benefit, and both sexes compete for the most profitable resource, leading to overlapping niches. John Wiley and Sons Inc. 2021-05-04 2021-08 /pmc/articles/PMC8453853/ /pubmed/33759459 http://dx.doi.org/10.1111/1365-2656.13487 Text en © 2021 The Authors. Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Li, Xiang‐Yi Kokko, Hanna Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? |
title | Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? |
title_full | Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? |
title_fullStr | Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? |
title_full_unstemmed | Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? |
title_short | Sexual dimorphism driven by intersexual resource competition: Why is it rare, and where to look for it? |
title_sort | sexual dimorphism driven by intersexual resource competition: why is it rare, and where to look for it? |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453853/ https://www.ncbi.nlm.nih.gov/pubmed/33759459 http://dx.doi.org/10.1111/1365-2656.13487 |
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