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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4598869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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