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Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization
Arbuscular mycorrhizal fungi (AMF) have evolved associations with roots of 60% plant species, but the net benefit for plants vary broadly from mutualism to parasitism. Yet, we lack a general understanding of the evolutionary and ecological forces driving such variation. To this end, we conducted a c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165190/ https://www.ncbi.nlm.nih.gov/pubmed/37168575 http://dx.doi.org/10.1016/j.isci.2023.106632 |
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author | Formenti, Ludovico Iwanycki Ahlstrand, Natalie Hassemer, Gustavo Glauser, Gaëtan van den Hoogen, Johan Rønsted, Nina van der Heijden, Marcel Crowther, Thomas W. Rasmann, Sergio |
author_facet | Formenti, Ludovico Iwanycki Ahlstrand, Natalie Hassemer, Gustavo Glauser, Gaëtan van den Hoogen, Johan Rønsted, Nina van der Heijden, Marcel Crowther, Thomas W. Rasmann, Sergio |
author_sort | Formenti, Ludovico |
collection | PubMed |
description | Arbuscular mycorrhizal fungi (AMF) have evolved associations with roots of 60% plant species, but the net benefit for plants vary broadly from mutualism to parasitism. Yet, we lack a general understanding of the evolutionary and ecological forces driving such variation. To this end, we conducted a comparative phylogenetic experiment with 24 species of Plantago, encompassing worldwide distribution, to address the effect of evolutionary history and environment on plant growth and chemical defenses in response to AMF colonization. We demonstrate that different species within one plant genus vary greatly in their ability to associate with AMF, and that AMF arbuscule colonization intensity decreases monotonically with increasing phylogenetic branch length, but not with concomitant changes in pedological and climatic conditions across species. Moreover, we demonstrate that species with the highest colonization levels are also those that change their defensive chemistry the least. We propose that the costs imposed by high AMF colonization in terms of reduced changes in secondary chemistry might drive the observed macroevolutionary decline in mycorrhization. |
format | Online Article Text |
id | pubmed-10165190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101651902023-05-09 Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization Formenti, Ludovico Iwanycki Ahlstrand, Natalie Hassemer, Gustavo Glauser, Gaëtan van den Hoogen, Johan Rønsted, Nina van der Heijden, Marcel Crowther, Thomas W. Rasmann, Sergio iScience Article Arbuscular mycorrhizal fungi (AMF) have evolved associations with roots of 60% plant species, but the net benefit for plants vary broadly from mutualism to parasitism. Yet, we lack a general understanding of the evolutionary and ecological forces driving such variation. To this end, we conducted a comparative phylogenetic experiment with 24 species of Plantago, encompassing worldwide distribution, to address the effect of evolutionary history and environment on plant growth and chemical defenses in response to AMF colonization. We demonstrate that different species within one plant genus vary greatly in their ability to associate with AMF, and that AMF arbuscule colonization intensity decreases monotonically with increasing phylogenetic branch length, but not with concomitant changes in pedological and climatic conditions across species. Moreover, we demonstrate that species with the highest colonization levels are also those that change their defensive chemistry the least. We propose that the costs imposed by high AMF colonization in terms of reduced changes in secondary chemistry might drive the observed macroevolutionary decline in mycorrhization. Elsevier 2023-04-10 /pmc/articles/PMC10165190/ /pubmed/37168575 http://dx.doi.org/10.1016/j.isci.2023.106632 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Formenti, Ludovico Iwanycki Ahlstrand, Natalie Hassemer, Gustavo Glauser, Gaëtan van den Hoogen, Johan Rønsted, Nina van der Heijden, Marcel Crowther, Thomas W. Rasmann, Sergio Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
title | Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
title_full | Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
title_fullStr | Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
title_full_unstemmed | Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
title_short | Macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
title_sort | macroevolutionary decline in mycorrhizal colonization and chemical defense responsiveness to mycorrhization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165190/ https://www.ncbi.nlm.nih.gov/pubmed/37168575 http://dx.doi.org/10.1016/j.isci.2023.106632 |
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