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Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects

Eusocial insects provide special opportunities to elucidate the evolution of ageing as queens have apparently evaded costs of reproduction and reversed the fecundity–longevity trade-off generally observed in non-social organisms. But how reproduction affects longevity in eusocial insects has rarely...

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Detalles Bibliográficos
Autores principales: Blacher, Pierre, Huggins, Timothy J., Bourke, Andrew F. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524490/
https://www.ncbi.nlm.nih.gov/pubmed/28701554
http://dx.doi.org/10.1098/rspb.2017.0380
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author Blacher, Pierre
Huggins, Timothy J.
Bourke, Andrew F. G.
author_facet Blacher, Pierre
Huggins, Timothy J.
Bourke, Andrew F. G.
author_sort Blacher, Pierre
collection PubMed
description Eusocial insects provide special opportunities to elucidate the evolution of ageing as queens have apparently evaded costs of reproduction and reversed the fecundity–longevity trade-off generally observed in non-social organisms. But how reproduction affects longevity in eusocial insects has rarely been tested experimentally. In this study, we took advantage of the reproductive plasticity of workers to test the causal role of reproduction in determining longevity in eusocial insects. Using the eusocial bumblebee Bombus terrestris, we found that, in whole colonies, in which workers could freely ‘choose’ whether to become reproductive, workers' level of ovarian activation was significantly positively associated with longevity and ovary-active workers significantly outlived ovary-inactive workers. By contrast, when reproductivity was experimentally induced in randomly selected workers, thereby decoupling it from other traits, workers' level of ovarian activation was significantly negatively associated with longevity and ovary-active workers were significantly less long-lived than ovary-inactive workers. These findings show that workers experience costs of reproduction and suggest that intrinsically high-quality individuals can overcome these costs. They also raise the possibility that eusocial insect queens exhibit condition-dependent longevity and hence call into question whether eusociality entails a truly reversed fecundity–longevity trade-off involving a fundamental remodelling of conserved genetic and endocrine networks underpinning ageing.
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spelling pubmed-55244902017-08-03 Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects Blacher, Pierre Huggins, Timothy J. Bourke, Andrew F. G. Proc Biol Sci Evolution Eusocial insects provide special opportunities to elucidate the evolution of ageing as queens have apparently evaded costs of reproduction and reversed the fecundity–longevity trade-off generally observed in non-social organisms. But how reproduction affects longevity in eusocial insects has rarely been tested experimentally. In this study, we took advantage of the reproductive plasticity of workers to test the causal role of reproduction in determining longevity in eusocial insects. Using the eusocial bumblebee Bombus terrestris, we found that, in whole colonies, in which workers could freely ‘choose’ whether to become reproductive, workers' level of ovarian activation was significantly positively associated with longevity and ovary-active workers significantly outlived ovary-inactive workers. By contrast, when reproductivity was experimentally induced in randomly selected workers, thereby decoupling it from other traits, workers' level of ovarian activation was significantly negatively associated with longevity and ovary-active workers were significantly less long-lived than ovary-inactive workers. These findings show that workers experience costs of reproduction and suggest that intrinsically high-quality individuals can overcome these costs. They also raise the possibility that eusocial insect queens exhibit condition-dependent longevity and hence call into question whether eusociality entails a truly reversed fecundity–longevity trade-off involving a fundamental remodelling of conserved genetic and endocrine networks underpinning ageing. The Royal Society 2017-07-12 2017-07-12 /pmc/articles/PMC5524490/ /pubmed/28701554 http://dx.doi.org/10.1098/rspb.2017.0380 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Blacher, Pierre
Huggins, Timothy J.
Bourke, Andrew F. G.
Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
title Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
title_full Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
title_fullStr Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
title_full_unstemmed Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
title_short Evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
title_sort evolution of ageing, costs of reproduction and the fecundity–longevity trade-off in eusocial insects
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524490/
https://www.ncbi.nlm.nih.gov/pubmed/28701554
http://dx.doi.org/10.1098/rspb.2017.0380
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