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Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa

Biotic stress can induce plastic changes in fitness-relevant plant traits. Recently, it has been shown that such changes can be transmitted to subsequent generations. However, the occurrence and extent of transmission across different types of traits is still unexplored. Here, we assessed the emerge...

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Autores principales: Kellenberger, Roman T., Desurmont, Gaylord A., Schlüter, Philipp M., Schiestl, Florian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824794/
https://www.ncbi.nlm.nih.gov/pubmed/29476119
http://dx.doi.org/10.1038/s41598-018-21880-2
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author Kellenberger, Roman T.
Desurmont, Gaylord A.
Schlüter, Philipp M.
Schiestl, Florian P.
author_facet Kellenberger, Roman T.
Desurmont, Gaylord A.
Schlüter, Philipp M.
Schiestl, Florian P.
author_sort Kellenberger, Roman T.
collection PubMed
description Biotic stress can induce plastic changes in fitness-relevant plant traits. Recently, it has been shown that such changes can be transmitted to subsequent generations. However, the occurrence and extent of transmission across different types of traits is still unexplored. Here, we assessed the emergence and transmission of herbivory-induced changes in Brassica rapa and their impact on interactions with insects. We analysed changes in morphology and reproductive traits as well as in flower and leaf volatile emission during two generations with leaf herbivory by Mamestra brassicae and Pieris brassicae and two subsequent generations without herbivory. Herbivory induced changes in all trait types, increasing attractiveness of the plants to the parasitoid wasp Cotesia glomerata and decreasing visitation by the pollinator Bombus terrestris, a potential trade-off. While changes in floral and leaf volatiles disappeared in the first generation after herbivory, some changes in morphology and reproductive traits were still measurable two generations after herbivory. However, neither parasitoids nor pollinators further discriminated between groups with different past treatments. Our results suggest that transmission of herbivore-induced changes occurs preferentially in resource-limited traits connected to plant growth and reproduction. The lack of alterations in plant-insect interactions was likely due to the transient nature of volatile changes.
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spelling pubmed-58247942018-03-01 Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa Kellenberger, Roman T. Desurmont, Gaylord A. Schlüter, Philipp M. Schiestl, Florian P. Sci Rep Article Biotic stress can induce plastic changes in fitness-relevant plant traits. Recently, it has been shown that such changes can be transmitted to subsequent generations. However, the occurrence and extent of transmission across different types of traits is still unexplored. Here, we assessed the emergence and transmission of herbivory-induced changes in Brassica rapa and their impact on interactions with insects. We analysed changes in morphology and reproductive traits as well as in flower and leaf volatile emission during two generations with leaf herbivory by Mamestra brassicae and Pieris brassicae and two subsequent generations without herbivory. Herbivory induced changes in all trait types, increasing attractiveness of the plants to the parasitoid wasp Cotesia glomerata and decreasing visitation by the pollinator Bombus terrestris, a potential trade-off. While changes in floral and leaf volatiles disappeared in the first generation after herbivory, some changes in morphology and reproductive traits were still measurable two generations after herbivory. However, neither parasitoids nor pollinators further discriminated between groups with different past treatments. Our results suggest that transmission of herbivore-induced changes occurs preferentially in resource-limited traits connected to plant growth and reproduction. The lack of alterations in plant-insect interactions was likely due to the transient nature of volatile changes. Nature Publishing Group UK 2018-02-23 /pmc/articles/PMC5824794/ /pubmed/29476119 http://dx.doi.org/10.1038/s41598-018-21880-2 Text en © The Author(s) 2018 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
Kellenberger, Roman T.
Desurmont, Gaylord A.
Schlüter, Philipp M.
Schiestl, Florian P.
Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa
title Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa
title_full Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa
title_fullStr Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa
title_full_unstemmed Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa
title_short Trans-generational inheritance of herbivory-induced phenotypic changes in Brassica rapa
title_sort trans-generational inheritance of herbivory-induced phenotypic changes in brassica rapa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824794/
https://www.ncbi.nlm.nih.gov/pubmed/29476119
http://dx.doi.org/10.1038/s41598-018-21880-2
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