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Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles
Male–female coevolution has taken different paths among closely related species, but our understanding of the factors that govern its direction is limited. While it is clear that ecological factors, life history, and the economics of reproduction are connected, the divergent links are often obscure....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388118/ https://www.ncbi.nlm.nih.gov/pubmed/35943983 http://dx.doi.org/10.1073/pnas.2205564119 |
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author | Arnqvist, Göran Rönn, Johanna Watson, Christopher Goenaga, Julieta Immonen, Elina |
author_facet | Arnqvist, Göran Rönn, Johanna Watson, Christopher Goenaga, Julieta Immonen, Elina |
author_sort | Arnqvist, Göran |
collection | PubMed |
description | Male–female coevolution has taken different paths among closely related species, but our understanding of the factors that govern its direction is limited. While it is clear that ecological factors, life history, and the economics of reproduction are connected, the divergent links are often obscure. We propose that a complete understanding requires the conceptual integration of metabolic phenotypes. Metabolic rate, a nexus of life history evolution, is constrained by ecological factors and may exert important direct and indirect effects on the evolution of sexual dimorphism. We performed standardized experiments in 12 seed beetle species to gain a rich set of sex-specific measures of metabolic phenotypes, life history traits, and the economics of mating and analyzed our multivariate data using phylogenetic comparative methods. Resting metabolic rate (RMR) showed extensive evolution and evolved more rapidly in males than in females. The evolution of RMR was tightly coupled with a suite of life history traits, describing a pace-of-life syndrome (POLS), with indirect effects on the economics of mating. As predicted, high resource competition was associated with a low RMR and a slow POLS. The cost of mating showed sexually antagonistic coevolution, a hallmark of sexual conflict. The sex-specific costs and benefits of mating were predictably related to ecology, primarily through the evolution of male ejaculate size. Overall, our results support the tenet that resource competition affects metabolic processes that, in turn, have predictable effects on both life history evolution and reproduction, such that ecology shows both direct and indirect effects on male–female coevolution. |
format | Online Article Text |
id | pubmed-9388118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-93881182022-08-19 Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles Arnqvist, Göran Rönn, Johanna Watson, Christopher Goenaga, Julieta Immonen, Elina Proc Natl Acad Sci U S A Biological Sciences Male–female coevolution has taken different paths among closely related species, but our understanding of the factors that govern its direction is limited. While it is clear that ecological factors, life history, and the economics of reproduction are connected, the divergent links are often obscure. We propose that a complete understanding requires the conceptual integration of metabolic phenotypes. Metabolic rate, a nexus of life history evolution, is constrained by ecological factors and may exert important direct and indirect effects on the evolution of sexual dimorphism. We performed standardized experiments in 12 seed beetle species to gain a rich set of sex-specific measures of metabolic phenotypes, life history traits, and the economics of mating and analyzed our multivariate data using phylogenetic comparative methods. Resting metabolic rate (RMR) showed extensive evolution and evolved more rapidly in males than in females. The evolution of RMR was tightly coupled with a suite of life history traits, describing a pace-of-life syndrome (POLS), with indirect effects on the economics of mating. As predicted, high resource competition was associated with a low RMR and a slow POLS. The cost of mating showed sexually antagonistic coevolution, a hallmark of sexual conflict. The sex-specific costs and benefits of mating were predictably related to ecology, primarily through the evolution of male ejaculate size. Overall, our results support the tenet that resource competition affects metabolic processes that, in turn, have predictable effects on both life history evolution and reproduction, such that ecology shows both direct and indirect effects on male–female coevolution. National Academy of Sciences 2022-08-09 2022-08-16 /pmc/articles/PMC9388118/ /pubmed/35943983 http://dx.doi.org/10.1073/pnas.2205564119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Arnqvist, Göran Rönn, Johanna Watson, Christopher Goenaga, Julieta Immonen, Elina Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
title | Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
title_full | Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
title_fullStr | Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
title_full_unstemmed | Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
title_short | Concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
title_sort | concerted evolution of metabolic rate, economics of mating, ecology, and pace of life across seed beetles |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388118/ https://www.ncbi.nlm.nih.gov/pubmed/35943983 http://dx.doi.org/10.1073/pnas.2205564119 |
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