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Annual egg productivity predicts female‐biased mortality in avian species
Among avian species, the differential cost entailed by either sex in competition for mates has been regarded as the main evolutionary influence on sex differences in mortality rates. However, empirical evidence suggests that sex‐biased adult mortality is mainly related to differential energy investm...
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/PMC9828124/ https://www.ncbi.nlm.nih.gov/pubmed/36117282 http://dx.doi.org/10.1111/evo.14623 |
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author | Romano, Andrea Liker, András Bazzi, Gaia Ambrosini, Roberto Møller, Anders P. Rubolini, Diego |
author_facet | Romano, Andrea Liker, András Bazzi, Gaia Ambrosini, Roberto Møller, Anders P. Rubolini, Diego |
author_sort | Romano, Andrea |
collection | PubMed |
description | Among avian species, the differential cost entailed by either sex in competition for mates has been regarded as the main evolutionary influence on sex differences in mortality rates. However, empirical evidence suggests that sex‐biased adult mortality is mainly related to differential energy investment in gamete production, with a greater annual mass devoted to egg production leading to higher female mortality. We explicitly tested the generality of this pattern in a comparative framework. Annual egg production can be relatively large in some species (up to 200% of female body mass) and annual mortality is generally biased toward females. We showed that greater annual egg productivity resulted in higher mortality rates of females relative to males. Mating system was secondarily important, with species in which males were more involved in mating competition having more equal mortality rates between the sexes. However, both traits explained only a limited fraction of the interspecific variation in female‐biased mortality. Other traits, such as sexual size dimorphism and parental care, had much weaker influences on female‐biased mortality. Our results suggest that both annual mass devoted to gamete production by females and mating system contribute to the evolution of the fundamental life‐history trade‐off between reproduction and survival in avian taxa. |
format | Online Article Text |
id | pubmed-9828124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98281242023-01-10 Annual egg productivity predicts female‐biased mortality in avian species Romano, Andrea Liker, András Bazzi, Gaia Ambrosini, Roberto Møller, Anders P. Rubolini, Diego Evolution Original Articles Among avian species, the differential cost entailed by either sex in competition for mates has been regarded as the main evolutionary influence on sex differences in mortality rates. However, empirical evidence suggests that sex‐biased adult mortality is mainly related to differential energy investment in gamete production, with a greater annual mass devoted to egg production leading to higher female mortality. We explicitly tested the generality of this pattern in a comparative framework. Annual egg production can be relatively large in some species (up to 200% of female body mass) and annual mortality is generally biased toward females. We showed that greater annual egg productivity resulted in higher mortality rates of females relative to males. Mating system was secondarily important, with species in which males were more involved in mating competition having more equal mortality rates between the sexes. However, both traits explained only a limited fraction of the interspecific variation in female‐biased mortality. Other traits, such as sexual size dimorphism and parental care, had much weaker influences on female‐biased mortality. Our results suggest that both annual mass devoted to gamete production by females and mating system contribute to the evolution of the fundamental life‐history trade‐off between reproduction and survival in avian taxa. John Wiley and Sons Inc. 2022-10-03 2022-11 /pmc/articles/PMC9828124/ /pubmed/36117282 http://dx.doi.org/10.1111/evo.14623 Text en © 2022 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 | Original Articles Romano, Andrea Liker, András Bazzi, Gaia Ambrosini, Roberto Møller, Anders P. Rubolini, Diego Annual egg productivity predicts female‐biased mortality in avian species |
title | Annual egg productivity predicts female‐biased mortality in avian species |
title_full | Annual egg productivity predicts female‐biased mortality in avian species |
title_fullStr | Annual egg productivity predicts female‐biased mortality in avian species |
title_full_unstemmed | Annual egg productivity predicts female‐biased mortality in avian species |
title_short | Annual egg productivity predicts female‐biased mortality in avian species |
title_sort | annual egg productivity predicts female‐biased mortality in avian species |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828124/ https://www.ncbi.nlm.nih.gov/pubmed/36117282 http://dx.doi.org/10.1111/evo.14623 |
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