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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-7920773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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