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Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation

Predators can induce phenotypic plasticity in prey through selection driven by predation risk. However, defense plasticity is rarely reported in insects, let alone trans-generational plasticity, meaning the mechanisms underlying plasticity, how it impacts ecosystem evolution and how it might be expl...

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Autores principales: Wen, Jian, Ueno, Takatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373946/
https://www.ncbi.nlm.nih.gov/pubmed/34408199
http://dx.doi.org/10.1038/s41598-021-96005-3
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author Wen, Jian
Ueno, Takatoshi
author_facet Wen, Jian
Ueno, Takatoshi
author_sort Wen, Jian
collection PubMed
description Predators can induce phenotypic plasticity in prey through selection driven by predation risk. However, defense plasticity is rarely reported in insects, let alone trans-generational plasticity, meaning the mechanisms underlying plasticity, how it impacts ecosystem evolution and how it might be exploited in pest control are poorly understood. Here we examine the morphological plasticity of small brown planthoppers (SBPHs), Laodelphax striatellus, elicited by caged predators, Paederus fuscipes in the parent or F1 generation and reveal the risk cues mediating these effects. We also uncover the survival outcomes in SBPHs with predator-induced defensive morphological traits by examining their survival probability and behavioral plasticity. Results showed that caged predators or predator odor cue gave rise to a higher proportion of long-winged, female SBPHs in the parent and F1 generations, but the proportion of males and their wing length were unaffected. The visual cue from predators elicited weaker effects. Surprisingly, we discovered these long-winged forms suffered a lower predation rate when attacked by P. fuscipes, owing to an enhanced agility level. Our results suggest the within- and trans-generational plasticity of induced defenses may cause profound effects on SBPH population dynamics and prey-predator interaction. Understanding this interaction and its underlying mechanisms illuminates important aspects of ecosystem evolution and helps predict pest dispersal or migration, which in turn may be exploited for pest control.
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spelling pubmed-83739462021-08-20 Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation Wen, Jian Ueno, Takatoshi Sci Rep Article Predators can induce phenotypic plasticity in prey through selection driven by predation risk. However, defense plasticity is rarely reported in insects, let alone trans-generational plasticity, meaning the mechanisms underlying plasticity, how it impacts ecosystem evolution and how it might be exploited in pest control are poorly understood. Here we examine the morphological plasticity of small brown planthoppers (SBPHs), Laodelphax striatellus, elicited by caged predators, Paederus fuscipes in the parent or F1 generation and reveal the risk cues mediating these effects. We also uncover the survival outcomes in SBPHs with predator-induced defensive morphological traits by examining their survival probability and behavioral plasticity. Results showed that caged predators or predator odor cue gave rise to a higher proportion of long-winged, female SBPHs in the parent and F1 generations, but the proportion of males and their wing length were unaffected. The visual cue from predators elicited weaker effects. Surprisingly, we discovered these long-winged forms suffered a lower predation rate when attacked by P. fuscipes, owing to an enhanced agility level. Our results suggest the within- and trans-generational plasticity of induced defenses may cause profound effects on SBPH population dynamics and prey-predator interaction. Understanding this interaction and its underlying mechanisms illuminates important aspects of ecosystem evolution and helps predict pest dispersal or migration, which in turn may be exploited for pest control. Nature Publishing Group UK 2021-08-18 /pmc/articles/PMC8373946/ /pubmed/34408199 http://dx.doi.org/10.1038/s41598-021-96005-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wen, Jian
Ueno, Takatoshi
Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
title Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
title_full Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
title_fullStr Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
title_full_unstemmed Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
title_short Predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
title_sort predator cue-induced plasticity of morphology and behavior in planthoppers facilitate the survival from predation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373946/
https://www.ncbi.nlm.nih.gov/pubmed/34408199
http://dx.doi.org/10.1038/s41598-021-96005-3
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