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The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga
Microbes form the base of food webs and drive biogeochemical cycling. Predicting the effects of microbial evolution on global elemental cycles remains a significant challenge due to the sheer number of interacting environmental and trait combinations. Here, we present an approach for integrating mul...
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/PMC8206706/ https://www.ncbi.nlm.nih.gov/pubmed/34130504 http://dx.doi.org/10.1098/rspb.2021.0940 |
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author | Walworth, Nathan G. Hinners, Jana Argyle, Phoebe A. Leles, Suzana G. Doblin, Martina A. Collins, Sinéad Levine, Naomi M. |
author_facet | Walworth, Nathan G. Hinners, Jana Argyle, Phoebe A. Leles, Suzana G. Doblin, Martina A. Collins, Sinéad Levine, Naomi M. |
author_sort | Walworth, Nathan G. |
collection | PubMed |
description | Microbes form the base of food webs and drive biogeochemical cycling. Predicting the effects of microbial evolution on global elemental cycles remains a significant challenge due to the sheer number of interacting environmental and trait combinations. Here, we present an approach for integrating multivariate trait data into a predictive model of trait evolution. We investigated the outcome of thousands of possible adaptive walks parameterized using empirical evolution data from the alga Chlamydomonas exposed to high CO(2). We found that the direction of historical bias (existing trait correlations) influenced both the rate of adaptation and the evolved phenotypes (trait combinations). Critically, we use fitness landscapes derived directly from empirical trait values to capture known evolutionary phenomena. This work demonstrates that ecological models need to represent both changes in traits and changes in the correlation between traits in order to accurately capture phytoplankton evolution and predict future shifts in elemental cycling. |
format | Online Article Text |
id | pubmed-8206706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82067062021-06-17 The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga Walworth, Nathan G. Hinners, Jana Argyle, Phoebe A. Leles, Suzana G. Doblin, Martina A. Collins, Sinéad Levine, Naomi M. Proc Biol Sci Evolution Microbes form the base of food webs and drive biogeochemical cycling. Predicting the effects of microbial evolution on global elemental cycles remains a significant challenge due to the sheer number of interacting environmental and trait combinations. Here, we present an approach for integrating multivariate trait data into a predictive model of trait evolution. We investigated the outcome of thousands of possible adaptive walks parameterized using empirical evolution data from the alga Chlamydomonas exposed to high CO(2). We found that the direction of historical bias (existing trait correlations) influenced both the rate of adaptation and the evolved phenotypes (trait combinations). Critically, we use fitness landscapes derived directly from empirical trait values to capture known evolutionary phenomena. This work demonstrates that ecological models need to represent both changes in traits and changes in the correlation between traits in order to accurately capture phytoplankton evolution and predict future shifts in elemental cycling. The Royal Society 2021-06-30 2021-06-16 /pmc/articles/PMC8206706/ /pubmed/34130504 http://dx.doi.org/10.1098/rspb.2021.0940 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 | Evolution Walworth, Nathan G. Hinners, Jana Argyle, Phoebe A. Leles, Suzana G. Doblin, Martina A. Collins, Sinéad Levine, Naomi M. The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga |
title | The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga |
title_full | The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga |
title_fullStr | The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga |
title_full_unstemmed | The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga |
title_short | The evolution of trait correlations constrains phenotypic adaptation to high CO(2) in a eukaryotic alga |
title_sort | evolution of trait correlations constrains phenotypic adaptation to high co(2) in a eukaryotic alga |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206706/ https://www.ncbi.nlm.nih.gov/pubmed/34130504 http://dx.doi.org/10.1098/rspb.2021.0940 |
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