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Male‐biased dispersal in a fungus‐gardening ant symbiosis

For nearly all organisms, dispersal is a fundamental life‐history trait that can shape their ecology and evolution. Variation in dispersal capabilities within a species exists and can influence population genetic structure and ecological interactions. In fungus‐gardening (attine) ants, co‐dispersal...

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Autores principales: Matthews, Alix E., Kellner, Katrin, Seal, Jon N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920773/
https://www.ncbi.nlm.nih.gov/pubmed/33717457
http://dx.doi.org/10.1002/ece3.7198
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author Matthews, Alix E.
Kellner, Katrin
Seal, Jon N.
author_facet Matthews, Alix E.
Kellner, Katrin
Seal, Jon N.
author_sort Matthews, Alix E.
collection PubMed
description For nearly all organisms, dispersal is a fundamental life‐history trait that can shape their ecology and evolution. Variation in dispersal capabilities within a species exists and can influence population genetic structure and ecological interactions. In fungus‐gardening (attine) ants, co‐dispersal of ants and mutualistic fungi is crucial to the success of this obligate symbiosis. Female‐biased dispersal (and gene flow) may be favored in attines because virgin queens carry the responsibility of dispersing the fungi, but a paucity of research has made this conclusion difficult. Here, we investigate dispersal of the fungus‐gardening ant Trachymyrmex septentrionalis using a combination of maternally (mitochondrial DNA) and biparentally inherited (microsatellites) markers. We found three distinct, spatially isolated mitochondrial DNA haplotypes; two were found in the Florida panhandle and the other in the Florida peninsula. In contrast, biparental markers illustrated significant gene flow across this region and minimal spatial structure. The differential patterns uncovered from mitochondrial DNA and microsatellite markers suggest that most long‐distance ant dispersal is male‐biased and that females (and concomitantly the fungus) have more limited dispersal capabilities. Consequently, the limited female dispersal is likely an important bottleneck for the fungal symbiont. This bottleneck could slow fungal genetic diversification, which has significant implications for both ant hosts and fungal symbionts regarding population genetics, species distributions, adaptive responses to environmental change, and coevolutionary patterns.
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spelling pubmed-79207732021-03-12 Male‐biased dispersal in a fungus‐gardening ant symbiosis Matthews, Alix E. Kellner, Katrin Seal, Jon N. Ecol Evol Original Research For nearly all organisms, dispersal is a fundamental life‐history trait that can shape their ecology and evolution. Variation in dispersal capabilities within a species exists and can influence population genetic structure and ecological interactions. In fungus‐gardening (attine) ants, co‐dispersal of ants and mutualistic fungi is crucial to the success of this obligate symbiosis. Female‐biased dispersal (and gene flow) may be favored in attines because virgin queens carry the responsibility of dispersing the fungi, but a paucity of research has made this conclusion difficult. Here, we investigate dispersal of the fungus‐gardening ant Trachymyrmex septentrionalis using a combination of maternally (mitochondrial DNA) and biparentally inherited (microsatellites) markers. We found three distinct, spatially isolated mitochondrial DNA haplotypes; two were found in the Florida panhandle and the other in the Florida peninsula. In contrast, biparental markers illustrated significant gene flow across this region and minimal spatial structure. The differential patterns uncovered from mitochondrial DNA and microsatellite markers suggest that most long‐distance ant dispersal is male‐biased and that females (and concomitantly the fungus) have more limited dispersal capabilities. Consequently, the limited female dispersal is likely an important bottleneck for the fungal symbiont. This bottleneck could slow fungal genetic diversification, which has significant implications for both ant hosts and fungal symbionts regarding population genetics, species distributions, adaptive responses to environmental change, and coevolutionary patterns. John Wiley and Sons Inc. 2021-01-28 /pmc/articles/PMC7920773/ /pubmed/33717457 http://dx.doi.org/10.1002/ece3.7198 Text en © 2021 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
Matthews, Alix E.
Kellner, Katrin
Seal, Jon N.
Male‐biased dispersal in a fungus‐gardening ant symbiosis
title Male‐biased dispersal in a fungus‐gardening ant symbiosis
title_full Male‐biased dispersal in a fungus‐gardening ant symbiosis
title_fullStr Male‐biased dispersal in a fungus‐gardening ant symbiosis
title_full_unstemmed Male‐biased dispersal in a fungus‐gardening ant symbiosis
title_short Male‐biased dispersal in a fungus‐gardening ant symbiosis
title_sort male‐biased dispersal in a fungus‐gardening ant symbiosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920773/
https://www.ncbi.nlm.nih.gov/pubmed/33717457
http://dx.doi.org/10.1002/ece3.7198
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