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Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations

Understanding patterns of gene flow and population structure is vital for managing threatened and endangered species. The reticulated flatwoods salamander (Ambystoma bishopi) is an endangered species with a fragmented range; therefore, assessing connectivity and genetic population structure can info...

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Autores principales: Williams, Steven T., Elbers, Jean P., Taylor, Sabrina 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/PMC8477597/
https://www.ncbi.nlm.nih.gov/pubmed/34603495
http://dx.doi.org/10.1111/eva.13287
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author Williams, Steven T.
Elbers, Jean P.
Taylor, Sabrina S.
author_facet Williams, Steven T.
Elbers, Jean P.
Taylor, Sabrina S.
author_sort Williams, Steven T.
collection PubMed
description Understanding patterns of gene flow and population structure is vital for managing threatened and endangered species. The reticulated flatwoods salamander (Ambystoma bishopi) is an endangered species with a fragmented range; therefore, assessing connectivity and genetic population structure can inform future conservation. Samples collected from breeding sites (n = 5) were used to calculate structure and gene flow using three marker types: single nucleotide polymorphisms isolated from potential immune genes (SNPs), nuclear data from the major histocompatibility complex (MHC), and the mitochondrial control region. At a broad geographical scale, nuclear data (SNP and MHC) supported gene flow and little structure (F (ST) = 0.00–0.09) while mitochondrial structure was high (Φ(ST) = 0.15–0.36) and gene flow was low. Mitochondrial markers also exhibited isolation by distance (IBD) between sites (p = 0.01) and within one site (p = 0.04) while nuclear markers did not show IBD between or within sites (p = 0.17 and p = 0.66). Due to the discordant results between nuclear and mitochondrial markers, our results suggest male‐biased dispersal. Overall, salamander populations showed little genetic differentiation and structure with some gene flow, at least historically, among sampling sites. Given historic gene flow and a lack of population structure, carefully considered reintroductions could begin to expand the limited range of this salamander to ensure its long‐term resilience.
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spelling pubmed-84775972021-10-01 Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations Williams, Steven T. Elbers, Jean P. Taylor, Sabrina S. Evol Appl Original Articles Understanding patterns of gene flow and population structure is vital for managing threatened and endangered species. The reticulated flatwoods salamander (Ambystoma bishopi) is an endangered species with a fragmented range; therefore, assessing connectivity and genetic population structure can inform future conservation. Samples collected from breeding sites (n = 5) were used to calculate structure and gene flow using three marker types: single nucleotide polymorphisms isolated from potential immune genes (SNPs), nuclear data from the major histocompatibility complex (MHC), and the mitochondrial control region. At a broad geographical scale, nuclear data (SNP and MHC) supported gene flow and little structure (F (ST) = 0.00–0.09) while mitochondrial structure was high (Φ(ST) = 0.15–0.36) and gene flow was low. Mitochondrial markers also exhibited isolation by distance (IBD) between sites (p = 0.01) and within one site (p = 0.04) while nuclear markers did not show IBD between or within sites (p = 0.17 and p = 0.66). Due to the discordant results between nuclear and mitochondrial markers, our results suggest male‐biased dispersal. Overall, salamander populations showed little genetic differentiation and structure with some gene flow, at least historically, among sampling sites. Given historic gene flow and a lack of population structure, carefully considered reintroductions could begin to expand the limited range of this salamander to ensure its long‐term resilience. John Wiley and Sons Inc. 2021-08-27 /pmc/articles/PMC8477597/ /pubmed/34603495 http://dx.doi.org/10.1111/eva.13287 Text en © 2021 The Authors. Evolutionary Applications 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 Articles
Williams, Steven T.
Elbers, Jean P.
Taylor, Sabrina S.
Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations
title Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations
title_full Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations
title_fullStr Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations
title_full_unstemmed Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations
title_short Population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (Ambystoma bishopi): Implications for translocations
title_sort population structure, gene flow, and sex‐biased dispersal in the reticulated flatwoods salamander (ambystoma bishopi): implications for translocations
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477597/
https://www.ncbi.nlm.nih.gov/pubmed/34603495
http://dx.doi.org/10.1111/eva.13287
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