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Experimental sexual selection affects the evolution of physiological and life‐history traits

Sexual selection and sexual conflict are expected to affect all aspects of the phenotype, not only traits that are directly involved in reproduction. Here, we show coordinated evolution of multiple physiological and life‐history traits in response to long‐term experimental manipulation of the mating...

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Autores principales: Garlovsky, Martin D., Holman, Luke, Brooks, Andrew L., Novicic, Zorana K., Snook, Rhonda R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322299/
https://www.ncbi.nlm.nih.gov/pubmed/35384100
http://dx.doi.org/10.1111/jeb.14003
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author Garlovsky, Martin D.
Holman, Luke
Brooks, Andrew L.
Novicic, Zorana K.
Snook, Rhonda R.
author_facet Garlovsky, Martin D.
Holman, Luke
Brooks, Andrew L.
Novicic, Zorana K.
Snook, Rhonda R.
author_sort Garlovsky, Martin D.
collection PubMed
description Sexual selection and sexual conflict are expected to affect all aspects of the phenotype, not only traits that are directly involved in reproduction. Here, we show coordinated evolution of multiple physiological and life‐history traits in response to long‐term experimental manipulation of the mating system in populations of Drosophila pseudoobscura. Development time was extended under polyandry relative to monogamy in both sexes, potentially due to higher investment in traits linked to sexual selection and sexual conflict. Individuals (especially males) evolving under polyandry had higher metabolic rates and locomotor activity than those evolving under monogamy. Polyandry individuals also invested more in metabolites associated with increased endurance capacity and efficient energy metabolism and regulation, namely lipids and glycogen. Finally, polyandry males were less desiccation‐ and starvation resistant than monogamy males, suggesting trade‐offs between resistance and sexually selected traits. Our results provide experimental evidence that mating systems can impose selection that influences the evolution of non‐sexual phenotypes such as development, activity, metabolism and nutrient homeostasis.
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spelling pubmed-93222992022-07-30 Experimental sexual selection affects the evolution of physiological and life‐history traits Garlovsky, Martin D. Holman, Luke Brooks, Andrew L. Novicic, Zorana K. Snook, Rhonda R. J Evol Biol Research Articles Sexual selection and sexual conflict are expected to affect all aspects of the phenotype, not only traits that are directly involved in reproduction. Here, we show coordinated evolution of multiple physiological and life‐history traits in response to long‐term experimental manipulation of the mating system in populations of Drosophila pseudoobscura. Development time was extended under polyandry relative to monogamy in both sexes, potentially due to higher investment in traits linked to sexual selection and sexual conflict. Individuals (especially males) evolving under polyandry had higher metabolic rates and locomotor activity than those evolving under monogamy. Polyandry individuals also invested more in metabolites associated with increased endurance capacity and efficient energy metabolism and regulation, namely lipids and glycogen. Finally, polyandry males were less desiccation‐ and starvation resistant than monogamy males, suggesting trade‐offs between resistance and sexually selected traits. Our results provide experimental evidence that mating systems can impose selection that influences the evolution of non‐sexual phenotypes such as development, activity, metabolism and nutrient homeostasis. John Wiley and Sons Inc. 2022-04-05 2022-05 /pmc/articles/PMC9322299/ /pubmed/35384100 http://dx.doi.org/10.1111/jeb.14003 Text en © 2022 The Authors. Journal of Evolutionary Biology published by John Wiley & Sons Ltd on behalf of European Society for Evolutionary Biology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Garlovsky, Martin D.
Holman, Luke
Brooks, Andrew L.
Novicic, Zorana K.
Snook, Rhonda R.
Experimental sexual selection affects the evolution of physiological and life‐history traits
title Experimental sexual selection affects the evolution of physiological and life‐history traits
title_full Experimental sexual selection affects the evolution of physiological and life‐history traits
title_fullStr Experimental sexual selection affects the evolution of physiological and life‐history traits
title_full_unstemmed Experimental sexual selection affects the evolution of physiological and life‐history traits
title_short Experimental sexual selection affects the evolution of physiological and life‐history traits
title_sort experimental sexual selection affects the evolution of physiological and life‐history traits
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322299/
https://www.ncbi.nlm.nih.gov/pubmed/35384100
http://dx.doi.org/10.1111/jeb.14003
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