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Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata

Disentangling pathways by which nonindigenous species expand and spread regionally remains challenging. Molecular ecology tools are often employed to determine the origins and spread of introduced species, but the complexities of some organisms may be reducing the efficacy of these tools. Some colon...

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Autores principales: Watts, Ashleigh Marie, Hopkins, Grant A., Goldstien, Sharyn Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434572/
https://www.ncbi.nlm.nih.gov/pubmed/30962883
http://dx.doi.org/10.1002/ece3.4817
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author Watts, Ashleigh Marie
Hopkins, Grant A.
Goldstien, Sharyn Jane
author_facet Watts, Ashleigh Marie
Hopkins, Grant A.
Goldstien, Sharyn Jane
author_sort Watts, Ashleigh Marie
collection PubMed
description Disentangling pathways by which nonindigenous species expand and spread regionally remains challenging. Molecular ecology tools are often employed to determine the origins and spread of introduced species, but the complexities of some organisms may be reducing the efficacy of these tools. Some colonial species exhibit complexities by way of chimerism and winter colony regression, which may alter the genetic diversity of populations and mask the connectivity occurring among them. This study uses nuclear microsatellite data and simple GIS‐based modeling to investigate the influence of chimerism and winter regression on the genetic diversity and patterns of genetic population connectivity among colonies of Didemnum vexillum on artificial substrates. Colonies sampled in summer were shown to form a metapopulation, with high levels of admixture, extreme outcrossing, and some substructure. These patterns were consistent within the subsampled winter colonies and with the inclusion of chimeric data. However, allelic richness and diversity were significantly different between winter and summer samples, altering interpretations relating to population connectivity and pelagic larval duration. This study demonstrates the importance of including seasonal sampling and imperative life history traits in genetic studies for clear interpretations and the successful management of introduced species.
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spelling pubmed-64345722019-04-08 Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata Watts, Ashleigh Marie Hopkins, Grant A. Goldstien, Sharyn Jane Ecol Evol Original Research Disentangling pathways by which nonindigenous species expand and spread regionally remains challenging. Molecular ecology tools are often employed to determine the origins and spread of introduced species, but the complexities of some organisms may be reducing the efficacy of these tools. Some colonial species exhibit complexities by way of chimerism and winter colony regression, which may alter the genetic diversity of populations and mask the connectivity occurring among them. This study uses nuclear microsatellite data and simple GIS‐based modeling to investigate the influence of chimerism and winter regression on the genetic diversity and patterns of genetic population connectivity among colonies of Didemnum vexillum on artificial substrates. Colonies sampled in summer were shown to form a metapopulation, with high levels of admixture, extreme outcrossing, and some substructure. These patterns were consistent within the subsampled winter colonies and with the inclusion of chimeric data. However, allelic richness and diversity were significantly different between winter and summer samples, altering interpretations relating to population connectivity and pelagic larval duration. This study demonstrates the importance of including seasonal sampling and imperative life history traits in genetic studies for clear interpretations and the successful management of introduced species. John Wiley and Sons Inc. 2019-02-21 /pmc/articles/PMC6434572/ /pubmed/30962883 http://dx.doi.org/10.1002/ece3.4817 Text en © 2019 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
Watts, Ashleigh Marie
Hopkins, Grant A.
Goldstien, Sharyn Jane
Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
title Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
title_full Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
title_fullStr Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
title_full_unstemmed Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
title_short Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
title_sort chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434572/
https://www.ncbi.nlm.nih.gov/pubmed/30962883
http://dx.doi.org/10.1002/ece3.4817
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