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Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort

BACKGROUND: The disposable soma theory of ageing assumes that organisms optimally trade-off limited resources between reproduction and longevity to maximize fitness. Early reproduction should especially trade-off against late reproduction and longevity because of reduced investment into somatic prot...

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Autores principales: Jehan, Charly, Chogne, Manon, Rigaud, Thierry, Moret, Yannick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998128/
https://www.ncbi.nlm.nih.gov/pubmed/32013878
http://dx.doi.org/10.1186/s12862-020-1586-x
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author Jehan, Charly
Chogne, Manon
Rigaud, Thierry
Moret, Yannick
author_facet Jehan, Charly
Chogne, Manon
Rigaud, Thierry
Moret, Yannick
author_sort Jehan, Charly
collection PubMed
description BACKGROUND: The disposable soma theory of ageing assumes that organisms optimally trade-off limited resources between reproduction and longevity to maximize fitness. Early reproduction should especially trade-off against late reproduction and longevity because of reduced investment into somatic protection, including immunity. Moreover, as optimal reproductive strategies of males and females differ, sexually dimorphic patterns of senescence may evolve. In particular, as males gain fitness through mating success, sexual competition should be a major factor accelerating male senescence. In a single experiment, we examined these possibilities by establishing artificial populations of the mealworm beetle, Tenebrio molitor, in which we manipulated the sex-ratio to generate variable levels of investment into reproductive effort and sexual competition in males and females. RESULTS: As predicted, variation in sex-ratio affected male and female reproductive efforts, with contrasted sex-specific trade-offs between lifetime reproduction, survival and immunity. High effort of reproduction accelerated mortality in females, without affecting immunity, but high early reproductive success was observed only in balanced sex-ratio condition. Male reproduction was costly on longevity and immunity, mainly because of their investment into copulations rather than in sexual competition. CONCLUSIONS: Our results suggest that T. molitor males, like females, maximize fitness through enhanced longevity, partly explaining their comparable longevity.
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spelling pubmed-69981282020-02-05 Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort Jehan, Charly Chogne, Manon Rigaud, Thierry Moret, Yannick BMC Evol Biol Research Article BACKGROUND: The disposable soma theory of ageing assumes that organisms optimally trade-off limited resources between reproduction and longevity to maximize fitness. Early reproduction should especially trade-off against late reproduction and longevity because of reduced investment into somatic protection, including immunity. Moreover, as optimal reproductive strategies of males and females differ, sexually dimorphic patterns of senescence may evolve. In particular, as males gain fitness through mating success, sexual competition should be a major factor accelerating male senescence. In a single experiment, we examined these possibilities by establishing artificial populations of the mealworm beetle, Tenebrio molitor, in which we manipulated the sex-ratio to generate variable levels of investment into reproductive effort and sexual competition in males and females. RESULTS: As predicted, variation in sex-ratio affected male and female reproductive efforts, with contrasted sex-specific trade-offs between lifetime reproduction, survival and immunity. High effort of reproduction accelerated mortality in females, without affecting immunity, but high early reproductive success was observed only in balanced sex-ratio condition. Male reproduction was costly on longevity and immunity, mainly because of their investment into copulations rather than in sexual competition. CONCLUSIONS: Our results suggest that T. molitor males, like females, maximize fitness through enhanced longevity, partly explaining their comparable longevity. BioMed Central 2020-02-03 /pmc/articles/PMC6998128/ /pubmed/32013878 http://dx.doi.org/10.1186/s12862-020-1586-x Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Jehan, Charly
Chogne, Manon
Rigaud, Thierry
Moret, Yannick
Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
title Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
title_full Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
title_fullStr Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
title_full_unstemmed Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
title_short Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
title_sort sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6998128/
https://www.ncbi.nlm.nih.gov/pubmed/32013878
http://dx.doi.org/10.1186/s12862-020-1586-x
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