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Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito
In temperate climates, the recurring seasonal exigencies of winter represent a fundamental physiological challenge for a wide range of organisms. In response, many temperate insects enter diapause, an alternative developmental program, including developmental arrest, that allows organisms to synchro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023039/ https://www.ncbi.nlm.nih.gov/pubmed/32490563 http://dx.doi.org/10.1111/evo.14029 |
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author | Batz, Zachary A. Clemento, Anthony J. Fritzenwanker, Jens Ring, Timothy J. Garza, John Carlos Armbruster, Peter A. |
author_facet | Batz, Zachary A. Clemento, Anthony J. Fritzenwanker, Jens Ring, Timothy J. Garza, John Carlos Armbruster, Peter A. |
author_sort | Batz, Zachary A. |
collection | PubMed |
description | In temperate climates, the recurring seasonal exigencies of winter represent a fundamental physiological challenge for a wide range of organisms. In response, many temperate insects enter diapause, an alternative developmental program, including developmental arrest, that allows organisms to synchronize their life cycle with seasonal environmental variation. Geographic variation in diapause phenology contributing to local climatic adaptation is well documented. However, few studies have examined how the rapid evolution of a suite of traits expressed across the diapause program may contribute to climatic adaptation on a contemporary timescale. Here, we investigate the evolution of the diapause program over the past 35 years by leveraging a “natural experiment” presented by the recent invasion of the Asian tiger mosquito, Aedes albopictus, across the eastern United States. We sampled populations from two distinct climatic regions separated by 6° of latitude (∼700 km). Using common‐garden experiments, we identified regional genetic divergence in diapause‐associated cold tolerance, diapause duration, and postdiapause starvation tolerance. We also found regional divergence in nondiapause thermal performance. In contrast, we observed minimal regional divergence in nondiapause larval growth traits and at neutral molecular marker loci. Our results demonstrate rapid evolution of the diapause program and imply strong selection caused by differences in winter conditions. |
format | Online Article Text |
id | pubmed-8023039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80230392021-04-07 Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito Batz, Zachary A. Clemento, Anthony J. Fritzenwanker, Jens Ring, Timothy J. Garza, John Carlos Armbruster, Peter A. Evolution Original Articles In temperate climates, the recurring seasonal exigencies of winter represent a fundamental physiological challenge for a wide range of organisms. In response, many temperate insects enter diapause, an alternative developmental program, including developmental arrest, that allows organisms to synchronize their life cycle with seasonal environmental variation. Geographic variation in diapause phenology contributing to local climatic adaptation is well documented. However, few studies have examined how the rapid evolution of a suite of traits expressed across the diapause program may contribute to climatic adaptation on a contemporary timescale. Here, we investigate the evolution of the diapause program over the past 35 years by leveraging a “natural experiment” presented by the recent invasion of the Asian tiger mosquito, Aedes albopictus, across the eastern United States. We sampled populations from two distinct climatic regions separated by 6° of latitude (∼700 km). Using common‐garden experiments, we identified regional genetic divergence in diapause‐associated cold tolerance, diapause duration, and postdiapause starvation tolerance. We also found regional divergence in nondiapause thermal performance. In contrast, we observed minimal regional divergence in nondiapause larval growth traits and at neutral molecular marker loci. Our results demonstrate rapid evolution of the diapause program and imply strong selection caused by differences in winter conditions. John Wiley and Sons Inc. 2020-06-16 2020-07 /pmc/articles/PMC8023039/ /pubmed/32490563 http://dx.doi.org/10.1111/evo.14029 Text en © 2020 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Batz, Zachary A. Clemento, Anthony J. Fritzenwanker, Jens Ring, Timothy J. Garza, John Carlos Armbruster, Peter A. Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
title | Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
title_full | Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
title_fullStr | Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
title_full_unstemmed | Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
title_short | Rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
title_sort | rapid adaptive evolution of the diapause program during range expansion of an invasive mosquito |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023039/ https://www.ncbi.nlm.nih.gov/pubmed/32490563 http://dx.doi.org/10.1111/evo.14029 |
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