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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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. |
format | Online Article Text |
id | pubmed-6590129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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