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Genomic dynamics of brown trout populations released to a novel environment
Population translocations occur for a variety of reasons, from displacement due to climate change to human‐induced transfers. Such actions have adverse effects on genetic variation and understanding their microevolutionary consequences requires monitoring. Here, we return to an experimental release...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251865/ https://www.ncbi.nlm.nih.gov/pubmed/35813906 http://dx.doi.org/10.1002/ece3.9050 |
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author | Kurland, Sara Rafati, Nima Ryman, Nils Laikre, Linda |
author_facet | Kurland, Sara Rafati, Nima Ryman, Nils Laikre, Linda |
author_sort | Kurland, Sara |
collection | PubMed |
description | Population translocations occur for a variety of reasons, from displacement due to climate change to human‐induced transfers. Such actions have adverse effects on genetic variation and understanding their microevolutionary consequences requires monitoring. Here, we return to an experimental release of brown trout (Salmo trutta) in order to monitor the genomic effects of population translocations. In 1979, fish from each of two genetically (F (ST) = 0.16) and ecologically separate populations were simultaneously released, at one point in time, to a lake system previously void of brown trout. Here, whole‐genome sequencing of pooled DNA (Pool‐seq) is used to characterize diversity within and divergence between the introduced populations and fish inhabiting two lakes downstream of the release sites, sampled 30 years later (c. 5 generations). Present results suggest that while extensive hybridization has occurred, the two introduced populations are unequally represented in the lakes downstream of the release sites. One population, which is ecologically resident in its original habitat, mainly contributes to the lake closest to the release site. The other population, migratory in its natal habitat, is genetically more represented in the lake further downstream. Genomic regions putatively under directional selection in the new habitat are identified, where allele frequencies in both established populations are more similar to the introduced population stemming from a resident population than the migratory one. Results suggest that the microevolutionary consequences of population translocations, for example, hybridization and adaptation, can be rapid and that Pool‐seq can be used as an initial tool to monitor genome‐wide effects. |
format | Online Article Text |
id | pubmed-9251865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92518652022-07-08 Genomic dynamics of brown trout populations released to a novel environment Kurland, Sara Rafati, Nima Ryman, Nils Laikre, Linda Ecol Evol Research Articles Population translocations occur for a variety of reasons, from displacement due to climate change to human‐induced transfers. Such actions have adverse effects on genetic variation and understanding their microevolutionary consequences requires monitoring. Here, we return to an experimental release of brown trout (Salmo trutta) in order to monitor the genomic effects of population translocations. In 1979, fish from each of two genetically (F (ST) = 0.16) and ecologically separate populations were simultaneously released, at one point in time, to a lake system previously void of brown trout. Here, whole‐genome sequencing of pooled DNA (Pool‐seq) is used to characterize diversity within and divergence between the introduced populations and fish inhabiting two lakes downstream of the release sites, sampled 30 years later (c. 5 generations). Present results suggest that while extensive hybridization has occurred, the two introduced populations are unequally represented in the lakes downstream of the release sites. One population, which is ecologically resident in its original habitat, mainly contributes to the lake closest to the release site. The other population, migratory in its natal habitat, is genetically more represented in the lake further downstream. Genomic regions putatively under directional selection in the new habitat are identified, where allele frequencies in both established populations are more similar to the introduced population stemming from a resident population than the migratory one. Results suggest that the microevolutionary consequences of population translocations, for example, hybridization and adaptation, can be rapid and that Pool‐seq can be used as an initial tool to monitor genome‐wide effects. John Wiley and Sons Inc. 2022-07-03 /pmc/articles/PMC9251865/ /pubmed/35813906 http://dx.doi.org/10.1002/ece3.9050 Text en © 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. 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 Kurland, Sara Rafati, Nima Ryman, Nils Laikre, Linda Genomic dynamics of brown trout populations released to a novel environment |
title | Genomic dynamics of brown trout populations released to a novel environment |
title_full | Genomic dynamics of brown trout populations released to a novel environment |
title_fullStr | Genomic dynamics of brown trout populations released to a novel environment |
title_full_unstemmed | Genomic dynamics of brown trout populations released to a novel environment |
title_short | Genomic dynamics of brown trout populations released to a novel environment |
title_sort | genomic dynamics of brown trout populations released to a novel environment |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251865/ https://www.ncbi.nlm.nih.gov/pubmed/35813906 http://dx.doi.org/10.1002/ece3.9050 |
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