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Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range
In recent decades Madagascar has experienced significant habitat loss and modification, with minimal understanding of how human land use practices have impacted the evolution of its flora and fauna. In light of ongoing and intensifying anthropogenic pressures, we seek new insight into mechanisms dri...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838192/ https://www.ncbi.nlm.nih.gov/pubmed/31700150 http://dx.doi.org/10.1038/s41598-019-52689-2 |
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author | Baden, Andrea L. Mancini, Amanda N. Federman, Sarah Holmes, Sheila M. Johnson, Steig E. Kamilar, Jason Louis, Edward E. Bradley, Brenda J. |
author_facet | Baden, Andrea L. Mancini, Amanda N. Federman, Sarah Holmes, Sheila M. Johnson, Steig E. Kamilar, Jason Louis, Edward E. Bradley, Brenda J. |
author_sort | Baden, Andrea L. |
collection | PubMed |
description | In recent decades Madagascar has experienced significant habitat loss and modification, with minimal understanding of how human land use practices have impacted the evolution of its flora and fauna. In light of ongoing and intensifying anthropogenic pressures, we seek new insight into mechanisms driving genetic variability on this island, using a Critically Endangered lemur species, the black-and-white ruffed lemur (Varecia variegata), as a test case. Here, we examine the relative influence of natural and anthropogenic landscape features that we predict will impose barriers to dispersal and promote genetic structuring across the species range. Using circuit theory, we model functional connectivity among 18 sampling localities using population-based genetic distance (F(ST)). We optimized resistance surfaces using genetic algorithms and assessed their performance using maximum-likelihood population-effects mixed models. The best supported resistance model was a composite surface that included two anthropogenic features, habitat cover and distance to villages, suggesting that rapid land cover modification by humans has driven change in the genetic structure of wild lemurs. Primary conservation priority should be placed on mitigating further forest loss and connecting regions identified as having low dispersal potential to prevent further loss of genetic diversity and promote the survival of other moist forest specialists. |
format | Online Article Text |
id | pubmed-6838192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68381922019-11-14 Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range Baden, Andrea L. Mancini, Amanda N. Federman, Sarah Holmes, Sheila M. Johnson, Steig E. Kamilar, Jason Louis, Edward E. Bradley, Brenda J. Sci Rep Article In recent decades Madagascar has experienced significant habitat loss and modification, with minimal understanding of how human land use practices have impacted the evolution of its flora and fauna. In light of ongoing and intensifying anthropogenic pressures, we seek new insight into mechanisms driving genetic variability on this island, using a Critically Endangered lemur species, the black-and-white ruffed lemur (Varecia variegata), as a test case. Here, we examine the relative influence of natural and anthropogenic landscape features that we predict will impose barriers to dispersal and promote genetic structuring across the species range. Using circuit theory, we model functional connectivity among 18 sampling localities using population-based genetic distance (F(ST)). We optimized resistance surfaces using genetic algorithms and assessed their performance using maximum-likelihood population-effects mixed models. The best supported resistance model was a composite surface that included two anthropogenic features, habitat cover and distance to villages, suggesting that rapid land cover modification by humans has driven change in the genetic structure of wild lemurs. Primary conservation priority should be placed on mitigating further forest loss and connecting regions identified as having low dispersal potential to prevent further loss of genetic diversity and promote the survival of other moist forest specialists. Nature Publishing Group UK 2019-11-07 /pmc/articles/PMC6838192/ /pubmed/31700150 http://dx.doi.org/10.1038/s41598-019-52689-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Baden, Andrea L. Mancini, Amanda N. Federman, Sarah Holmes, Sheila M. Johnson, Steig E. Kamilar, Jason Louis, Edward E. Bradley, Brenda J. Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range |
title | Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range |
title_full | Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range |
title_fullStr | Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range |
title_full_unstemmed | Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range |
title_short | Anthropogenic pressures drive population genetic structuring across a Critically Endangered lemur species range |
title_sort | anthropogenic pressures drive population genetic structuring across a critically endangered lemur species range |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838192/ https://www.ncbi.nlm.nih.gov/pubmed/31700150 http://dx.doi.org/10.1038/s41598-019-52689-2 |
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