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Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish

Interpreting contemporary patterns of population structure requires an understanding of the interactions among microevolutionary forces and past demographic events. Here, 4,122 SNP‐containing loci were used to assess structure in southern flounder (Paralichthys lethostigma) sampled across its range...

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Autores principales: O'Leary, Shannon J., Hollenbeck, Christopher M., Vega, Robert R., Portnoy, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495835/
https://www.ncbi.nlm.nih.gov/pubmed/34646479
http://dx.doi.org/10.1002/ece3.8064
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author O'Leary, Shannon J.
Hollenbeck, Christopher M.
Vega, Robert R.
Portnoy, David S.
author_facet O'Leary, Shannon J.
Hollenbeck, Christopher M.
Vega, Robert R.
Portnoy, David S.
author_sort O'Leary, Shannon J.
collection PubMed
description Interpreting contemporary patterns of population structure requires an understanding of the interactions among microevolutionary forces and past demographic events. Here, 4,122 SNP‐containing loci were used to assess structure in southern flounder (Paralichthys lethostigma) sampled across its range in the US Atlantic Ocean (Atlantic) and Gulf of Mexico (Gulf) and relationships among components of genomic variation and spatial and environmental variables were assessed across estuarine population samples in the Gulf. While hierarchical amova revealed significant heterogeneity within and between the Atlantic and Gulf, pairwise comparisons between samples within ocean basins demonstrated that all significant heterogeneity occurred within the Gulf. The distribution of Tajima's D estimated at a genome‐wide scale differed significantly from equilibrium in all estuaries, with more negative values occurring in the Gulf. Components of genomic variation were significantly associated with environmental variables describing individual estuaries, and environment explained a larger component of variation than spatial proximity. Overall, results suggest that there is genetic spatial autocorrelation caused by shared larval sources for proximal nurseries (migration/drift), but that it is modified by environmentally driven differentiation (selection). This leads to conflicting signals in different parts of the genome and creates patterns of divergence that do not correspond to paradigms of strong local directional selection.
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spelling pubmed-84958352021-10-12 Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish O'Leary, Shannon J. Hollenbeck, Christopher M. Vega, Robert R. Portnoy, David S. Ecol Evol Original Research Interpreting contemporary patterns of population structure requires an understanding of the interactions among microevolutionary forces and past demographic events. Here, 4,122 SNP‐containing loci were used to assess structure in southern flounder (Paralichthys lethostigma) sampled across its range in the US Atlantic Ocean (Atlantic) and Gulf of Mexico (Gulf) and relationships among components of genomic variation and spatial and environmental variables were assessed across estuarine population samples in the Gulf. While hierarchical amova revealed significant heterogeneity within and between the Atlantic and Gulf, pairwise comparisons between samples within ocean basins demonstrated that all significant heterogeneity occurred within the Gulf. The distribution of Tajima's D estimated at a genome‐wide scale differed significantly from equilibrium in all estuaries, with more negative values occurring in the Gulf. Components of genomic variation were significantly associated with environmental variables describing individual estuaries, and environment explained a larger component of variation than spatial proximity. Overall, results suggest that there is genetic spatial autocorrelation caused by shared larval sources for proximal nurseries (migration/drift), but that it is modified by environmentally driven differentiation (selection). This leads to conflicting signals in different parts of the genome and creates patterns of divergence that do not correspond to paradigms of strong local directional selection. John Wiley and Sons Inc. 2021-08-30 /pmc/articles/PMC8495835/ /pubmed/34646479 http://dx.doi.org/10.1002/ece3.8064 Text en © 2021 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 Original Research
O'Leary, Shannon J.
Hollenbeck, Christopher M.
Vega, Robert R.
Portnoy, David S.
Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
title Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
title_full Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
title_fullStr Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
title_full_unstemmed Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
title_short Disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
title_sort disentangling complex genomic signals to understand population structure of an exploited, estuarine‐dependent flatfish
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495835/
https://www.ncbi.nlm.nih.gov/pubmed/34646479
http://dx.doi.org/10.1002/ece3.8064
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