Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783252476498018304 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5524490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT blacherpierre evolutionofageingcostsofreproductionandthefecunditylongevitytradeoffineusocialinsects AT hugginstimothyj evolutionofageingcostsofreproductionandthefecunditylongevitytradeoffineusocialinsects AT bourkeandrewfg evolutionofageingcostsofreproductionandthefecunditylongevitytradeoffineusocialinsects |