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Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites

Predation risk is a strong selective force shaping prey morphology, life history and behavior. Anti-predator behaviors may be innate, learned or both but little is known about the transgenerational behavioral effects of maternally experienced predation risk. We examined intraguild predation (IGP) ri...

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Autores principales: Seiter, Michael, Schausberger, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598869/
https://www.ncbi.nlm.nih.gov/pubmed/26449645
http://dx.doi.org/10.1038/srep15046
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author Seiter, Michael
Schausberger, Peter
author_facet Seiter, Michael
Schausberger, Peter
author_sort Seiter, Michael
collection PubMed
description Predation risk is a strong selective force shaping prey morphology, life history and behavior. Anti-predator behaviors may be innate, learned or both but little is known about the transgenerational behavioral effects of maternally experienced predation risk. We examined intraguild predation (IGP) risk-induced maternal effects on offspring anti-predator behavior, including learning, in the predatory mite Phytoseiulus persimilis. We exposed predatory mite mothers during egg production to presence or absence of the IG predator Amblyseius andersoni and assessed whether maternal stress affects the anti-predator behavior, including larval learning ability, of their offspring as protonymphs. Protonymphs emerging from stressed or unstressed mothers, and having experienced IGP risk as larvae or not, were subjected to choice situations with and without IG predator traces. Predator-experienced protonymphs from stressed mothers were the least active and acted the boldest in site choice towards predator cues. We argue that the attenuated response of the protonymphs to predator traces alone represents optimized risk management because no immediate risk existed. Such behavioral adjustment could reduce the inherent fitness costs of anti-predator behaviors. Overall, our study suggests that P. persimilis mothers experiencing IGP risk may prime their offspring to behave more optimally in IGP environments.
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spelling pubmed-45988692015-10-13 Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites Seiter, Michael Schausberger, Peter Sci Rep Article Predation risk is a strong selective force shaping prey morphology, life history and behavior. Anti-predator behaviors may be innate, learned or both but little is known about the transgenerational behavioral effects of maternally experienced predation risk. We examined intraguild predation (IGP) risk-induced maternal effects on offspring anti-predator behavior, including learning, in the predatory mite Phytoseiulus persimilis. We exposed predatory mite mothers during egg production to presence or absence of the IG predator Amblyseius andersoni and assessed whether maternal stress affects the anti-predator behavior, including larval learning ability, of their offspring as protonymphs. Protonymphs emerging from stressed or unstressed mothers, and having experienced IGP risk as larvae or not, were subjected to choice situations with and without IG predator traces. Predator-experienced protonymphs from stressed mothers were the least active and acted the boldest in site choice towards predator cues. We argue that the attenuated response of the protonymphs to predator traces alone represents optimized risk management because no immediate risk existed. Such behavioral adjustment could reduce the inherent fitness costs of anti-predator behaviors. Overall, our study suggests that P. persimilis mothers experiencing IGP risk may prime their offspring to behave more optimally in IGP environments. Nature Publishing Group 2015-10-09 /pmc/articles/PMC4598869/ /pubmed/26449645 http://dx.doi.org/10.1038/srep15046 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Seiter, Michael
Schausberger, Peter
Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
title Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
title_full Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
title_fullStr Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
title_full_unstemmed Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
title_short Maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
title_sort maternal intraguild predation risk affects offspring anti-predator behavior and learning in mites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598869/
https://www.ncbi.nlm.nih.gov/pubmed/26449645
http://dx.doi.org/10.1038/srep15046
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