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Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect

The disposable soma theory of ageing predicts that when organisms invest in reproduction they do so by reducing their investment in body maintenance, inducing a trade‐off between reproduction and survival. Experiments on invertebrates in the lab provide support for the theory by demonstrating the pr...

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Autores principales: Rodríguez‐Muñoz, Rolando, Boonekamp, Jelle J., Liu, Xing P., Skicko, Ian, Fisher, David N., Hopwood, Paul, Tregenza, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590129/
https://www.ncbi.nlm.nih.gov/pubmed/30597559
http://dx.doi.org/10.1111/evo.13679
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author Rodríguez‐Muñoz, Rolando
Boonekamp, Jelle J.
Liu, Xing P.
Skicko, Ian
Fisher, David N.
Hopwood, Paul
Tregenza, Tom
author_facet Rodríguez‐Muñoz, Rolando
Boonekamp, Jelle J.
Liu, Xing P.
Skicko, Ian
Fisher, David N.
Hopwood, Paul
Tregenza, Tom
author_sort Rodríguez‐Muñoz, Rolando
collection PubMed
description The disposable soma theory of ageing predicts that when organisms invest in reproduction they do so by reducing their investment in body maintenance, inducing a trade‐off between reproduction and survival. Experiments on invertebrates in the lab provide support for the theory by demonstrating the predicted responses to manipulation of reproductive effort or lifespan. However, experimental studies in birds and evidence from observational (nonmanipulative) studies in nature do not consistently reveal trade‐offs. Most species studied previously in the wild are mammals and birds that reproduce over multiple discrete seasons. This contrasts with temperate invertebrates, which typically have annual generations and reproduce over a single season. We expand the taxonomic range of senescence study systems to include life histories typical of most temperate invertebrates. We monitored reproductive effort, ageing, and survival in a natural field cricket population over ten years to test the prediction that individuals investing more in early‐reproduction senesce faster and die younger. We found no evidence of a trade‐off between early‐life reproductive effort and survival, and only weak evidence for a trade‐off with phenotypic senescence. We discuss the possibility that organisms with multiple discrete breeding seasons may have greater opportunities to express trade‐offs between reproduction and senescence.
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spelling pubmed-65901292019-07-08 Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect Rodríguez‐Muñoz, Rolando Boonekamp, Jelle J. Liu, Xing P. Skicko, Ian Fisher, David N. Hopwood, Paul Tregenza, Tom Evolution Original Articles The disposable soma theory of ageing predicts that when organisms invest in reproduction they do so by reducing their investment in body maintenance, inducing a trade‐off between reproduction and survival. Experiments on invertebrates in the lab provide support for the theory by demonstrating the predicted responses to manipulation of reproductive effort or lifespan. However, experimental studies in birds and evidence from observational (nonmanipulative) studies in nature do not consistently reveal trade‐offs. Most species studied previously in the wild are mammals and birds that reproduce over multiple discrete seasons. This contrasts with temperate invertebrates, which typically have annual generations and reproduce over a single season. We expand the taxonomic range of senescence study systems to include life histories typical of most temperate invertebrates. We monitored reproductive effort, ageing, and survival in a natural field cricket population over ten years to test the prediction that individuals investing more in early‐reproduction senesce faster and die younger. We found no evidence of a trade‐off between early‐life reproductive effort and survival, and only weak evidence for a trade‐off with phenotypic senescence. We discuss the possibility that organisms with multiple discrete breeding seasons may have greater opportunities to express trade‐offs between reproduction and senescence. John Wiley and Sons Inc. 2019-01-10 2019-02 /pmc/articles/PMC6590129/ /pubmed/30597559 http://dx.doi.org/10.1111/evo.13679 Text en © 2018 The Author(s). Evolution published by Wiley Periodicals, Inc. on behalf of The Society for the Study of Evolution. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rodríguez‐Muñoz, Rolando
Boonekamp, Jelle J.
Liu, Xing P.
Skicko, Ian
Fisher, David N.
Hopwood, Paul
Tregenza, Tom
Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
title Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
title_full Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
title_fullStr Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
title_full_unstemmed Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
title_short Testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
title_sort testing the effect of early‐life reproductive effort on age‐related decline in a wild insect
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590129/
https://www.ncbi.nlm.nih.gov/pubmed/30597559
http://dx.doi.org/10.1111/evo.13679
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