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Chemical cannibalistic cues make damselfly larvae hide rather than hunt
Adopting cannibalism substantially affects individual fitness, and recognizing the presence of other cannibals provides additional benefits such as the opportunity to prepare for hunting or defense. This recognition can be facilitated by perceiving conspecific chemical cues. Their role in cannibalis...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442433/ https://www.ncbi.nlm.nih.gov/pubmed/37604994 http://dx.doi.org/10.1038/s41598-023-40732-2 |
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author | Sysiak, Monika Pietrzak, Barbara Kubiak, Matylda Bednarska, Anna Mikulski, Andrzej |
author_facet | Sysiak, Monika Pietrzak, Barbara Kubiak, Matylda Bednarska, Anna Mikulski, Andrzej |
author_sort | Sysiak, Monika |
collection | PubMed |
description | Adopting cannibalism substantially affects individual fitness, and recognizing the presence of other cannibals provides additional benefits such as the opportunity to prepare for hunting or defense. This recognition can be facilitated by perceiving conspecific chemical cues. Their role in cannibalistic interactions is less studied than in interspecific predation and it is unclear whether these cues inform individuals of danger or of food availability. Interpretation of these cues is crucial to balance the costs and benefits of anti-predator and feeding strategies, which can directly influence individual fitness. In this study we aimed to test whether damselfly larvae shift towards bolder and more exploratory (cannibalistic) behavior, or become more careful to avoid potential cannibals (as prey) in response to such cues. We conducted behavioral and respiratory experiments with Ischnura elegans larvae to investigate their response to chemical cues from older and larger conspecific larvae. We found that I. elegans larvae decrease their activity and shift their respiratory-related behavior, indicating activation of anti-predator defense mechanisms in response to conspecific chemical cues. Our findings indicate that individuals exposed to conspecific chemical cues balance catching prey with staying safe. |
format | Online Article Text |
id | pubmed-10442433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104424332023-08-23 Chemical cannibalistic cues make damselfly larvae hide rather than hunt Sysiak, Monika Pietrzak, Barbara Kubiak, Matylda Bednarska, Anna Mikulski, Andrzej Sci Rep Article Adopting cannibalism substantially affects individual fitness, and recognizing the presence of other cannibals provides additional benefits such as the opportunity to prepare for hunting or defense. This recognition can be facilitated by perceiving conspecific chemical cues. Their role in cannibalistic interactions is less studied than in interspecific predation and it is unclear whether these cues inform individuals of danger or of food availability. Interpretation of these cues is crucial to balance the costs and benefits of anti-predator and feeding strategies, which can directly influence individual fitness. In this study we aimed to test whether damselfly larvae shift towards bolder and more exploratory (cannibalistic) behavior, or become more careful to avoid potential cannibals (as prey) in response to such cues. We conducted behavioral and respiratory experiments with Ischnura elegans larvae to investigate their response to chemical cues from older and larger conspecific larvae. We found that I. elegans larvae decrease their activity and shift their respiratory-related behavior, indicating activation of anti-predator defense mechanisms in response to conspecific chemical cues. Our findings indicate that individuals exposed to conspecific chemical cues balance catching prey with staying safe. Nature Publishing Group UK 2023-08-21 /pmc/articles/PMC10442433/ /pubmed/37604994 http://dx.doi.org/10.1038/s41598-023-40732-2 Text en © The Author(s) 2023 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 Sysiak, Monika Pietrzak, Barbara Kubiak, Matylda Bednarska, Anna Mikulski, Andrzej Chemical cannibalistic cues make damselfly larvae hide rather than hunt |
title | Chemical cannibalistic cues make damselfly larvae hide rather than hunt |
title_full | Chemical cannibalistic cues make damselfly larvae hide rather than hunt |
title_fullStr | Chemical cannibalistic cues make damselfly larvae hide rather than hunt |
title_full_unstemmed | Chemical cannibalistic cues make damselfly larvae hide rather than hunt |
title_short | Chemical cannibalistic cues make damselfly larvae hide rather than hunt |
title_sort | chemical cannibalistic cues make damselfly larvae hide rather than hunt |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442433/ https://www.ncbi.nlm.nih.gov/pubmed/37604994 http://dx.doi.org/10.1038/s41598-023-40732-2 |
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