Cargando…

Tritrophic interactions follow phylogenetic escalation and climatic adaptation

One major goal in plant evolutionary ecology is to address how and why tritrophic interactions mediated by phytochemical plant defences vary across species, space, and time. In this study, we tested three classical hypotheses about plant defences: (i) the resource-availability hypothesis, (ii) the a...

Descripción completa

Detalles Bibliográficos
Autores principales: Kergunteuil, Alan, Humair, Laureline, Maire, Anne-Laure, Moreno-Aguilar, María Fernanda, Godschalx, Adrienne, Catalán, Pilar, Rasmann, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005781/
https://www.ncbi.nlm.nih.gov/pubmed/32034273
http://dx.doi.org/10.1038/s41598-020-59068-2
_version_ 1783495009448755200
author Kergunteuil, Alan
Humair, Laureline
Maire, Anne-Laure
Moreno-Aguilar, María Fernanda
Godschalx, Adrienne
Catalán, Pilar
Rasmann, Sergio
author_facet Kergunteuil, Alan
Humair, Laureline
Maire, Anne-Laure
Moreno-Aguilar, María Fernanda
Godschalx, Adrienne
Catalán, Pilar
Rasmann, Sergio
author_sort Kergunteuil, Alan
collection PubMed
description One major goal in plant evolutionary ecology is to address how and why tritrophic interactions mediated by phytochemical plant defences vary across species, space, and time. In this study, we tested three classical hypotheses about plant defences: (i) the resource-availability hypothesis, (ii) the altitudinal/elevational gradient hypothesis and (iii) the defence escalation hypothesis. For this purpose, predatory soil nematodes were challenged to hunt for root herbivores based on volatile cues from damaged or intact roots of 18 Alpine Festuca grass species adapted to distinct climatic niches spanning 2000 meters of elevation. We found that adaptation into harsh, nutrient-limited alpine environments coincided with the production of specific blends of volatiles, highly attractive for nematodes. We also found that recently-diverged taxa exposed to herbivores released higher amounts of volatiles than ancestrally-diverged species. Therefore, our model provides evidence that belowground indirect plant defences associated with tritrophic interactions have evolved under two classical hypotheses in plant ecology. While phylogenetic drivers of volatile emissions point to the defence-escalation hypothesis, plant local adaptation of indirect defences is in line with the resource availability hypothesis.
format Online
Article
Text
id pubmed-7005781
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70057812020-02-18 Tritrophic interactions follow phylogenetic escalation and climatic adaptation Kergunteuil, Alan Humair, Laureline Maire, Anne-Laure Moreno-Aguilar, María Fernanda Godschalx, Adrienne Catalán, Pilar Rasmann, Sergio Sci Rep Article One major goal in plant evolutionary ecology is to address how and why tritrophic interactions mediated by phytochemical plant defences vary across species, space, and time. In this study, we tested three classical hypotheses about plant defences: (i) the resource-availability hypothesis, (ii) the altitudinal/elevational gradient hypothesis and (iii) the defence escalation hypothesis. For this purpose, predatory soil nematodes were challenged to hunt for root herbivores based on volatile cues from damaged or intact roots of 18 Alpine Festuca grass species adapted to distinct climatic niches spanning 2000 meters of elevation. We found that adaptation into harsh, nutrient-limited alpine environments coincided with the production of specific blends of volatiles, highly attractive for nematodes. We also found that recently-diverged taxa exposed to herbivores released higher amounts of volatiles than ancestrally-diverged species. Therefore, our model provides evidence that belowground indirect plant defences associated with tritrophic interactions have evolved under two classical hypotheses in plant ecology. While phylogenetic drivers of volatile emissions point to the defence-escalation hypothesis, plant local adaptation of indirect defences is in line with the resource availability hypothesis. Nature Publishing Group UK 2020-02-07 /pmc/articles/PMC7005781/ /pubmed/32034273 http://dx.doi.org/10.1038/s41598-020-59068-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kergunteuil, Alan
Humair, Laureline
Maire, Anne-Laure
Moreno-Aguilar, María Fernanda
Godschalx, Adrienne
Catalán, Pilar
Rasmann, Sergio
Tritrophic interactions follow phylogenetic escalation and climatic adaptation
title Tritrophic interactions follow phylogenetic escalation and climatic adaptation
title_full Tritrophic interactions follow phylogenetic escalation and climatic adaptation
title_fullStr Tritrophic interactions follow phylogenetic escalation and climatic adaptation
title_full_unstemmed Tritrophic interactions follow phylogenetic escalation and climatic adaptation
title_short Tritrophic interactions follow phylogenetic escalation and climatic adaptation
title_sort tritrophic interactions follow phylogenetic escalation and climatic adaptation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005781/
https://www.ncbi.nlm.nih.gov/pubmed/32034273
http://dx.doi.org/10.1038/s41598-020-59068-2
work_keys_str_mv AT kergunteuilalan tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation
AT humairlaureline tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation
AT maireannelaure tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation
AT morenoaguilarmariafernanda tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation
AT godschalxadrienne tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation
AT catalanpilar tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation
AT rasmannsergio tritrophicinteractionsfollowphylogeneticescalationandclimaticadaptation