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Plant‐associate interactions and diversification across trophic levels

Interactions between species are widely understood to have promoted the diversification of life on Earth, but how interactions spur the formation of new species remains unclear. Interacting species often become locally adapted to each other, but they may also be subject to shared dispersal limitatio...

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Autores principales: Yoder, Jeremy B., Dang, Albert, MacGregor, Caitlin, Plaza, Mikhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554764/
https://www.ncbi.nlm.nih.gov/pubmed/36254257
http://dx.doi.org/10.1002/evl3.296
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author Yoder, Jeremy B.
Dang, Albert
MacGregor, Caitlin
Plaza, Mikhail
author_facet Yoder, Jeremy B.
Dang, Albert
MacGregor, Caitlin
Plaza, Mikhail
author_sort Yoder, Jeremy B.
collection PubMed
description Interactions between species are widely understood to have promoted the diversification of life on Earth, but how interactions spur the formation of new species remains unclear. Interacting species often become locally adapted to each other, but they may also be subject to shared dispersal limitations and environmental conditions. Moreover, theory predicts that different kinds of interactions have different effects on diversification. To better understand how species interactions promote diversification, we compiled population genetic studies of host plants and intimately associated herbivores, parasites, and mutualists. We used Bayesian multiple regressions and the BEDASSLE modeling framework to test whether host and associate population structures were correlated over and above the potentially confounding effects of geography and shared environmental variation. We found that associates' population structure often paralleled their hosts' population structure, and that this effect is robust to accounting for geographic distance and climate. Associate genetic structure was significantly explained by plant genetic structure somewhat more often in antagonistic interactions than in mutualistic ones. This aligns with a key prediction of coevolutionary theory that antagonistic interactions promote diversity through local adaptation of antagonists to hosts, while mutualistic interactions more often promote diversity via the effect of hosts' geographic distribution on mutualists' dispersal.
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spelling pubmed-95547642022-10-16 Plant‐associate interactions and diversification across trophic levels Yoder, Jeremy B. Dang, Albert MacGregor, Caitlin Plaza, Mikhail Evol Lett Letters Interactions between species are widely understood to have promoted the diversification of life on Earth, but how interactions spur the formation of new species remains unclear. Interacting species often become locally adapted to each other, but they may also be subject to shared dispersal limitations and environmental conditions. Moreover, theory predicts that different kinds of interactions have different effects on diversification. To better understand how species interactions promote diversification, we compiled population genetic studies of host plants and intimately associated herbivores, parasites, and mutualists. We used Bayesian multiple regressions and the BEDASSLE modeling framework to test whether host and associate population structures were correlated over and above the potentially confounding effects of geography and shared environmental variation. We found that associates' population structure often paralleled their hosts' population structure, and that this effect is robust to accounting for geographic distance and climate. Associate genetic structure was significantly explained by plant genetic structure somewhat more often in antagonistic interactions than in mutualistic ones. This aligns with a key prediction of coevolutionary theory that antagonistic interactions promote diversity through local adaptation of antagonists to hosts, while mutualistic interactions more often promote diversity via the effect of hosts' geographic distribution on mutualists' dispersal. John Wiley and Sons Inc. 2022-09-18 /pmc/articles/PMC9554764/ /pubmed/36254257 http://dx.doi.org/10.1002/evl3.296 Text en © 2022 The Authors. Evolution Letters published by Wiley Periodicals LLC on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Yoder, Jeremy B.
Dang, Albert
MacGregor, Caitlin
Plaza, Mikhail
Plant‐associate interactions and diversification across trophic levels
title Plant‐associate interactions and diversification across trophic levels
title_full Plant‐associate interactions and diversification across trophic levels
title_fullStr Plant‐associate interactions and diversification across trophic levels
title_full_unstemmed Plant‐associate interactions and diversification across trophic levels
title_short Plant‐associate interactions and diversification across trophic levels
title_sort plant‐associate interactions and diversification across trophic levels
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554764/
https://www.ncbi.nlm.nih.gov/pubmed/36254257
http://dx.doi.org/10.1002/evl3.296
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