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Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish
Paternal age and past mating effort by males are often confounded, which can affect our understanding of a father's age effects. To our knowledge, only a few studies have standardized mating history when testing for effects of paternal age, and none has simultaneously disentangled how paternal...
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/PMC9543789/ https://www.ncbi.nlm.nih.gov/pubmed/35544673 http://dx.doi.org/10.1111/evo.14498 |
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author | Aich, Upama Chowdhury, Shawan Jennions, Michael D. |
author_facet | Aich, Upama Chowdhury, Shawan Jennions, Michael D. |
author_sort | Aich, Upama |
collection | PubMed |
description | Paternal age and past mating effort by males are often confounded, which can affect our understanding of a father's age effects. To our knowledge, only a few studies have standardized mating history when testing for effects of paternal age, and none has simultaneously disentangled how paternal age and mating history might jointly influence offspring traits. Here, we experimentally manipulated male mating history to tease apart its effects from those of paternal age on female fertility and offspring traits in the eastern mosquitofish (Gambusia holbrooki). Male age did not affect female fertility. However, males with greater past mating effort produced significantly larger broods. Paternal age and mating history interacted to affect sons' body size: sons sired by old‐virgin males were larger than those sired by old‐mated males, but this was not the case for younger fathers. Intriguingly, however, sons sired by old‐virgin males tended to produce fewer sperms than those sired by old‐mated males, indicating a potential trade‐off in beneficial paternal effects. Finally, neither paternal age nor mating history affected daughter's fitness. Our results highlight that variation in offspring traits attributed to paternal age effect could partly arise due to a father's mating history, and not simply to his chronological age. |
format | Online Article Text |
id | pubmed-9543789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95437892022-10-14 Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish Aich, Upama Chowdhury, Shawan Jennions, Michael D. Evolution Original Articles Paternal age and past mating effort by males are often confounded, which can affect our understanding of a father's age effects. To our knowledge, only a few studies have standardized mating history when testing for effects of paternal age, and none has simultaneously disentangled how paternal age and mating history might jointly influence offspring traits. Here, we experimentally manipulated male mating history to tease apart its effects from those of paternal age on female fertility and offspring traits in the eastern mosquitofish (Gambusia holbrooki). Male age did not affect female fertility. However, males with greater past mating effort produced significantly larger broods. Paternal age and mating history interacted to affect sons' body size: sons sired by old‐virgin males were larger than those sired by old‐mated males, but this was not the case for younger fathers. Intriguingly, however, sons sired by old‐virgin males tended to produce fewer sperms than those sired by old‐mated males, indicating a potential trade‐off in beneficial paternal effects. Finally, neither paternal age nor mating history affected daughter's fitness. Our results highlight that variation in offspring traits attributed to paternal age effect could partly arise due to a father's mating history, and not simply to his chronological age. John Wiley and Sons Inc. 2022-05-18 2022-07 /pmc/articles/PMC9543789/ /pubmed/35544673 http://dx.doi.org/10.1111/evo.14498 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-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 | Original Articles Aich, Upama Chowdhury, Shawan Jennions, Michael D. Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish |
title | Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish |
title_full | Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish |
title_fullStr | Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish |
title_full_unstemmed | Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish |
title_short | Separating the effects of paternal age and mating history: Evidence for sex‐specific paternal effect in eastern mosquitofish |
title_sort | separating the effects of paternal age and mating history: evidence for sex‐specific paternal effect in eastern mosquitofish |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543789/ https://www.ncbi.nlm.nih.gov/pubmed/35544673 http://dx.doi.org/10.1111/evo.14498 |
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