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Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient

As the rate of urbanization continues to increase globally, a growing body of research is emerging that investigates how urbanization shapes the movement—and consequent gene flow—of species in cities. Of particular interest are native species that persist in cities, either as small relict population...

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Autores principales: Richardson, Jonathan L., Michaelides, Sozos, Combs, Matthew, Djan, Mihajla, Bisch, Lianne, Barrett, Kerry, Silveira, Georgianna, Butler, Justin, Aye, Than Thar, Munshi‐South, Jason, DiMatteo, Michael, Brown, Charles, McGreevy, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819555/
https://www.ncbi.nlm.nih.gov/pubmed/33519963
http://dx.doi.org/10.1111/eva.13133
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author Richardson, Jonathan L.
Michaelides, Sozos
Combs, Matthew
Djan, Mihajla
Bisch, Lianne
Barrett, Kerry
Silveira, Georgianna
Butler, Justin
Aye, Than Thar
Munshi‐South, Jason
DiMatteo, Michael
Brown, Charles
McGreevy, Thomas J.
author_facet Richardson, Jonathan L.
Michaelides, Sozos
Combs, Matthew
Djan, Mihajla
Bisch, Lianne
Barrett, Kerry
Silveira, Georgianna
Butler, Justin
Aye, Than Thar
Munshi‐South, Jason
DiMatteo, Michael
Brown, Charles
McGreevy, Thomas J.
author_sort Richardson, Jonathan L.
collection PubMed
description As the rate of urbanization continues to increase globally, a growing body of research is emerging that investigates how urbanization shapes the movement—and consequent gene flow—of species in cities. Of particular interest are native species that persist in cities, either as small relict populations or as larger populations of synanthropic species that thrive alongside humans in new urban environments. In this study, we used genomic sequence data (SNPs) and spatially explicit individual‐based analyses to directly compare the genetic structure and patterns of gene flow in two small mammals with different dispersal abilities that occupy the same urbanized landscape to evaluate how mobility impacts genetic connectivity. We collected 215 white‐footed mice (Peromyscus leucopus) and 380 big brown bats (Eptesicus fuscus) across an urban‐to‐rural gradient within the Providence, Rhode Island (U.S.A.) metropolitan area (population =1,600,000 people). We found that mice and bats exhibit clear differences in their spatial genetic structure that are consistent with their dispersal abilities, with urbanization having a stronger effect on Peromyscus mice. There were sharp breaks in the genetic structure of mice within the Providence urban core, as well as reduced rates of migration and an increase in inbreeding with more urbanization. In contrast, bats showed very weak genetic structuring across the entire study area, suggesting a near‐panmictic gene pool likely due to the ability to disperse by flight. Genetic diversity remained stable for both species across the study region. Mice also exhibited a stronger reduction in gene flow between island and mainland populations than bats. This study represents one of the first to directly compare multiple species within the same urban‐to‐rural landscape gradient, an important gap to fill for urban ecology and evolution. Moreover, here we document the impacts of dispersal capacity on connectivity for native species that have persisted as the urban landscape matrix expands.
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spelling pubmed-78195552021-01-29 Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient Richardson, Jonathan L. Michaelides, Sozos Combs, Matthew Djan, Mihajla Bisch, Lianne Barrett, Kerry Silveira, Georgianna Butler, Justin Aye, Than Thar Munshi‐South, Jason DiMatteo, Michael Brown, Charles McGreevy, Thomas J. Evol Appl Special Issue Original Articles As the rate of urbanization continues to increase globally, a growing body of research is emerging that investigates how urbanization shapes the movement—and consequent gene flow—of species in cities. Of particular interest are native species that persist in cities, either as small relict populations or as larger populations of synanthropic species that thrive alongside humans in new urban environments. In this study, we used genomic sequence data (SNPs) and spatially explicit individual‐based analyses to directly compare the genetic structure and patterns of gene flow in two small mammals with different dispersal abilities that occupy the same urbanized landscape to evaluate how mobility impacts genetic connectivity. We collected 215 white‐footed mice (Peromyscus leucopus) and 380 big brown bats (Eptesicus fuscus) across an urban‐to‐rural gradient within the Providence, Rhode Island (U.S.A.) metropolitan area (population =1,600,000 people). We found that mice and bats exhibit clear differences in their spatial genetic structure that are consistent with their dispersal abilities, with urbanization having a stronger effect on Peromyscus mice. There were sharp breaks in the genetic structure of mice within the Providence urban core, as well as reduced rates of migration and an increase in inbreeding with more urbanization. In contrast, bats showed very weak genetic structuring across the entire study area, suggesting a near‐panmictic gene pool likely due to the ability to disperse by flight. Genetic diversity remained stable for both species across the study region. Mice also exhibited a stronger reduction in gene flow between island and mainland populations than bats. This study represents one of the first to directly compare multiple species within the same urban‐to‐rural landscape gradient, an important gap to fill for urban ecology and evolution. Moreover, here we document the impacts of dispersal capacity on connectivity for native species that have persisted as the urban landscape matrix expands. John Wiley and Sons Inc. 2020-11-06 /pmc/articles/PMC7819555/ /pubmed/33519963 http://dx.doi.org/10.1111/eva.13133 Text en © 2020 The Authors. Evolutionary Applications 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 Special Issue Original Articles
Richardson, Jonathan L.
Michaelides, Sozos
Combs, Matthew
Djan, Mihajla
Bisch, Lianne
Barrett, Kerry
Silveira, Georgianna
Butler, Justin
Aye, Than Thar
Munshi‐South, Jason
DiMatteo, Michael
Brown, Charles
McGreevy, Thomas J.
Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
title Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
title_full Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
title_fullStr Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
title_full_unstemmed Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
title_short Dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
title_sort dispersal ability predicts spatial genetic structure in native mammals persisting across an urbanization gradient
topic Special Issue Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819555/
https://www.ncbi.nlm.nih.gov/pubmed/33519963
http://dx.doi.org/10.1111/eva.13133
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