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Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults

Barrow’s goldeneyes across western North America have been shown to have a high degree of subpopulation independence using several data types. However, evidence for structured populations based on mitochondrial DNA, band recoveries, and tracking of adults is discordant with evidence from autosomal D...

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Autores principales: Forstner, T. M., Boyd, W. S., Esler, D., Green, D. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568906/
https://www.ncbi.nlm.nih.gov/pubmed/37822000
http://dx.doi.org/10.1186/s40462-023-00423-z
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author Forstner, T. M.
Boyd, W. S.
Esler, D.
Green, D. J.
author_facet Forstner, T. M.
Boyd, W. S.
Esler, D.
Green, D. J.
author_sort Forstner, T. M.
collection PubMed
description Barrow’s goldeneyes across western North America have been shown to have a high degree of subpopulation independence using several data types. However, evidence for structured populations based on mitochondrial DNA, band recoveries, and tracking of adults is discordant with evidence from autosomal DNA. We used satellite tracking data from both juveniles and adults marked on natal and breeding grounds, respectively, in British Columbia, Canada to evaluate the hypothesis that male-biased juvenile dispersal maintains genetic panmixia of Pacific Barrow’s goldeneyes otherwise structured by migratory movements and high winter and breeding site fidelity of adults. We found that juvenile males traveled to overwintering sites located within the range of the overwintering sites of juvenile females, adult males, and adult females. Juvenile males migrated at the same time, travelled the same distance when moving between natal and overwintering sites, and had the same winter dispersion as juvenile females. Although juveniles did not travel with attendant females, all juveniles overwintered within the wintering range of adults. We tracked some juveniles into the following spring/summer and even second winter. Prospecting juveniles of both sexes travelled from their wintering grounds to potential breeding sites in the proximity of Riske Creek and within the bounds of the breeding locations used by adults. Juveniles tracked for more than a year also showed relatively high winter site fidelity. Because Barrow’s goldeneyes pair on wintering grounds, our tracking data are not consistent with the hypothesis that male-biased juvenile dispersal explains the genetic structure in the mitochondrial DNA and panmixia in the autosomal DNA of Barrow’s goldeneye. We suggest that uncommon or episodic dispersal of males might be enough to homogenize autosomal DNA but is unlikely to influence demographic population structure relevant to contemporary population management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40462-023-00423-z.
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spelling pubmed-105689062023-10-13 Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults Forstner, T. M. Boyd, W. S. Esler, D. Green, D. J. Mov Ecol Research Barrow’s goldeneyes across western North America have been shown to have a high degree of subpopulation independence using several data types. However, evidence for structured populations based on mitochondrial DNA, band recoveries, and tracking of adults is discordant with evidence from autosomal DNA. We used satellite tracking data from both juveniles and adults marked on natal and breeding grounds, respectively, in British Columbia, Canada to evaluate the hypothesis that male-biased juvenile dispersal maintains genetic panmixia of Pacific Barrow’s goldeneyes otherwise structured by migratory movements and high winter and breeding site fidelity of adults. We found that juvenile males traveled to overwintering sites located within the range of the overwintering sites of juvenile females, adult males, and adult females. Juvenile males migrated at the same time, travelled the same distance when moving between natal and overwintering sites, and had the same winter dispersion as juvenile females. Although juveniles did not travel with attendant females, all juveniles overwintered within the wintering range of adults. We tracked some juveniles into the following spring/summer and even second winter. Prospecting juveniles of both sexes travelled from their wintering grounds to potential breeding sites in the proximity of Riske Creek and within the bounds of the breeding locations used by adults. Juveniles tracked for more than a year also showed relatively high winter site fidelity. Because Barrow’s goldeneyes pair on wintering grounds, our tracking data are not consistent with the hypothesis that male-biased juvenile dispersal explains the genetic structure in the mitochondrial DNA and panmixia in the autosomal DNA of Barrow’s goldeneye. We suggest that uncommon or episodic dispersal of males might be enough to homogenize autosomal DNA but is unlikely to influence demographic population structure relevant to contemporary population management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40462-023-00423-z. BioMed Central 2023-10-12 /pmc/articles/PMC10568906/ /pubmed/37822000 http://dx.doi.org/10.1186/s40462-023-00423-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Forstner, T. M.
Boyd, W. S.
Esler, D.
Green, D. J.
Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults
title Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults
title_full Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults
title_fullStr Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults
title_full_unstemmed Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults
title_short Dispersal of juvenile Barrow’s goldeneyes (Bucephala islandica) mirrors that of breeding adults
title_sort dispersal of juvenile barrow’s goldeneyes (bucephala islandica) mirrors that of breeding adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568906/
https://www.ncbi.nlm.nih.gov/pubmed/37822000
http://dx.doi.org/10.1186/s40462-023-00423-z
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