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Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds

Population increases over the past several decades provide natural settings in which to study the evolutionary processes that occur during bottleneck, growth, and spatial expansion. We used parallel natural experiments of historical decline and subsequent recovery in two sympatric pinniped species i...

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Autores principales: Cammen, Kristina M., Schultz, Thomas F., Don Bowen, W., Hammill, Michael O., Puryear, Wendy B., Runstadler, Jonathan, Wenzel, Frederick W., Wood, Stephanie A., Kinnison, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053562/
https://www.ncbi.nlm.nih.gov/pubmed/30038760
http://dx.doi.org/10.1002/ece3.4143
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author Cammen, Kristina M.
Schultz, Thomas F.
Don Bowen, W.
Hammill, Michael O.
Puryear, Wendy B.
Runstadler, Jonathan
Wenzel, Frederick W.
Wood, Stephanie A.
Kinnison, Michael
author_facet Cammen, Kristina M.
Schultz, Thomas F.
Don Bowen, W.
Hammill, Michael O.
Puryear, Wendy B.
Runstadler, Jonathan
Wenzel, Frederick W.
Wood, Stephanie A.
Kinnison, Michael
author_sort Cammen, Kristina M.
collection PubMed
description Population increases over the past several decades provide natural settings in which to study the evolutionary processes that occur during bottleneck, growth, and spatial expansion. We used parallel natural experiments of historical decline and subsequent recovery in two sympatric pinniped species in the Northwest Atlantic, the gray seal (Halichoerus grypus atlantica) and harbor seal (Phoca vitulina vitulina), to study the impact of recent demographic change in genomic diversity. Using restriction site‐associated DNA sequencing, we assessed genomic diversity at over 8,700 polymorphic gray seal loci and 3,700 polymorphic harbor seal loci in samples from multiple cohorts collected throughout recovery over the past half‐century. Despite significant differences in the degree of genetic diversity assessed in the two species, we found signatures of historical bottlenecks in the contemporary genomes of both gray and harbor seals. We evaluated temporal trends in diversity across cohorts, as well as compared samples from sites at both the center and edge of a recent gray seal range expansion, but found no significant change in genomewide diversity following recovery. We did, however, find that the variance and degree of allele frequency change measured over the past several decades were significantly different from neutral expectations of drift under population growth. These two cases of well‐described demographic history provide opportunities for critical evaluation of current approaches to simulating and understanding the genetic effects of historical demographic change in natural populations.
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spelling pubmed-60535622018-07-23 Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds Cammen, Kristina M. Schultz, Thomas F. Don Bowen, W. Hammill, Michael O. Puryear, Wendy B. Runstadler, Jonathan Wenzel, Frederick W. Wood, Stephanie A. Kinnison, Michael Ecol Evol Original Research Population increases over the past several decades provide natural settings in which to study the evolutionary processes that occur during bottleneck, growth, and spatial expansion. We used parallel natural experiments of historical decline and subsequent recovery in two sympatric pinniped species in the Northwest Atlantic, the gray seal (Halichoerus grypus atlantica) and harbor seal (Phoca vitulina vitulina), to study the impact of recent demographic change in genomic diversity. Using restriction site‐associated DNA sequencing, we assessed genomic diversity at over 8,700 polymorphic gray seal loci and 3,700 polymorphic harbor seal loci in samples from multiple cohorts collected throughout recovery over the past half‐century. Despite significant differences in the degree of genetic diversity assessed in the two species, we found signatures of historical bottlenecks in the contemporary genomes of both gray and harbor seals. We evaluated temporal trends in diversity across cohorts, as well as compared samples from sites at both the center and edge of a recent gray seal range expansion, but found no significant change in genomewide diversity following recovery. We did, however, find that the variance and degree of allele frequency change measured over the past several decades were significantly different from neutral expectations of drift under population growth. These two cases of well‐described demographic history provide opportunities for critical evaluation of current approaches to simulating and understanding the genetic effects of historical demographic change in natural populations. John Wiley and Sons Inc. 2018-06-05 /pmc/articles/PMC6053562/ /pubmed/30038760 http://dx.doi.org/10.1002/ece3.4143 Text en © 2018 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://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
Cammen, Kristina M.
Schultz, Thomas F.
Don Bowen, W.
Hammill, Michael O.
Puryear, Wendy B.
Runstadler, Jonathan
Wenzel, Frederick W.
Wood, Stephanie A.
Kinnison, Michael
Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds
title Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds
title_full Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds
title_fullStr Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds
title_full_unstemmed Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds
title_short Genomic signatures of population bottleneck and recovery in Northwest Atlantic pinnipeds
title_sort genomic signatures of population bottleneck and recovery in northwest atlantic pinnipeds
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053562/
https://www.ncbi.nlm.nih.gov/pubmed/30038760
http://dx.doi.org/10.1002/ece3.4143
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