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...
Autores principales: | , , , , , , |
---|---|
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 |