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Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime
Metabolism defines the energetic cost of life, yet we still know relatively little about why intraspecific variation in metabolic rate arises and persists. Spatio-temporal variation in selection potentially maintains differences, but relationships between metabolic traits (standard metabolic rate (S...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441116/ https://www.ncbi.nlm.nih.gov/pubmed/34521251 http://dx.doi.org/10.1098/rspb.2021.1509 |
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author | Archer, Louise C. Hutton, Stephen A. Harman, Luke Russell Poole, W. Gargan, Patrick McGinnity, Philip Reed, Thomas E. |
author_facet | Archer, Louise C. Hutton, Stephen A. Harman, Luke Russell Poole, W. Gargan, Patrick McGinnity, Philip Reed, Thomas E. |
author_sort | Archer, Louise C. |
collection | PubMed |
description | Metabolism defines the energetic cost of life, yet we still know relatively little about why intraspecific variation in metabolic rate arises and persists. Spatio-temporal variation in selection potentially maintains differences, but relationships between metabolic traits (standard metabolic rate (SMR), maximum metabolic rate (MMR), and aerobic scope) and fitness across contexts are unresolved. We show that associations between SMR, MMR, and growth rate (a key fitness-related trait) vary depending on the thermal regime (a potential selective agent) in offspring of wild-sampled brown trout from two populations reared for approximately 15 months in either a cool or warm (+1.8°C) regime. SMR was positively related to growth in the cool, but negatively related in the warm regime. The opposite patterns were found for MMR and growth associations (positive in warm, negative in the cool regime). Mean SMR, but not MMR, was lower in warm regimes within both populations (i.e. basal metabolic costs were reduced at higher temperatures), consistent with an adaptive acclimation response that optimizes growth. Metabolic phenotypes thus exhibited a thermally sensitive metabolic ‘floor’ and a less flexible metabolic ‘ceiling’. Our findings suggest a role for growth-related fluctuating selection in shaping patterns of metabolic variation that is likely important in adapting to climate change. |
format | Online Article Text |
id | pubmed-8441116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84411162021-09-22 Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime Archer, Louise C. Hutton, Stephen A. Harman, Luke Russell Poole, W. Gargan, Patrick McGinnity, Philip Reed, Thomas E. Proc Biol Sci Ecology Metabolism defines the energetic cost of life, yet we still know relatively little about why intraspecific variation in metabolic rate arises and persists. Spatio-temporal variation in selection potentially maintains differences, but relationships between metabolic traits (standard metabolic rate (SMR), maximum metabolic rate (MMR), and aerobic scope) and fitness across contexts are unresolved. We show that associations between SMR, MMR, and growth rate (a key fitness-related trait) vary depending on the thermal regime (a potential selective agent) in offspring of wild-sampled brown trout from two populations reared for approximately 15 months in either a cool or warm (+1.8°C) regime. SMR was positively related to growth in the cool, but negatively related in the warm regime. The opposite patterns were found for MMR and growth associations (positive in warm, negative in the cool regime). Mean SMR, but not MMR, was lower in warm regimes within both populations (i.e. basal metabolic costs were reduced at higher temperatures), consistent with an adaptive acclimation response that optimizes growth. Metabolic phenotypes thus exhibited a thermally sensitive metabolic ‘floor’ and a less flexible metabolic ‘ceiling’. Our findings suggest a role for growth-related fluctuating selection in shaping patterns of metabolic variation that is likely important in adapting to climate change. The Royal Society 2021-09-08 2021-09-15 /pmc/articles/PMC8441116/ /pubmed/34521251 http://dx.doi.org/10.1098/rspb.2021.1509 Text en © 2021 The Authors. https://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/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Ecology Archer, Louise C. Hutton, Stephen A. Harman, Luke Russell Poole, W. Gargan, Patrick McGinnity, Philip Reed, Thomas E. Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime |
title | Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime |
title_full | Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime |
title_fullStr | Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime |
title_full_unstemmed | Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime |
title_short | Associations between metabolic traits and growth rate in brown trout (Salmo trutta) depend on thermal regime |
title_sort | associations between metabolic traits and growth rate in brown trout (salmo trutta) depend on thermal regime |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441116/ https://www.ncbi.nlm.nih.gov/pubmed/34521251 http://dx.doi.org/10.1098/rspb.2021.1509 |
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