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Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure

Attempts to control invasive species using species-specific pheromones need to incorporate an understanding of interactive effects among those pathways. The larvae of invasive cane toads (Rhinella marina) utilise chemical cues to repulse, attract or suppress conspecific larvae. We can exploit these...

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Autores principales: McCann, Samantha, Crossland, Michael, Shine, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259751/
https://www.ncbi.nlm.nih.gov/pubmed/32469938
http://dx.doi.org/10.1371/journal.pone.0233653
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author McCann, Samantha
Crossland, Michael
Shine, Richard
author_facet McCann, Samantha
Crossland, Michael
Shine, Richard
author_sort McCann, Samantha
collection PubMed
description Attempts to control invasive species using species-specific pheromones need to incorporate an understanding of interactive effects among those pathways. The larvae of invasive cane toads (Rhinella marina) utilise chemical cues to repulse, attract or suppress conspecific larvae. We can exploit these effects to reduce toad abundance, but the effects of each cue may not be additive. That is, exposure to one type of cue may lessen the impact of exposure to another cue. To assess this possibility, we exposed toad larvae to combinations of cues. Tadpoles that had been exposed to the suppression cue during larval development exhibited no response to the attraction cue, resulting in lower capture rates in attractant-baited traps. Suppression, however, did not affect a tadpole’s response to the alarm cue, and exposure to the alarm cue during tadpole development did not affect response to the attraction cue. Tadpoles exposed to the suppression cue were smaller than control tadpoles at 10 days post-exposure, and consequently were more vulnerable to gape-limited invertebrate predators. Our results demonstrate that the responses by toad tadpoles to chemical cues interact in important ways, and are not simply additive when combined. Control efforts need to incorporate an understanding of such interactions if we are to most effectively use chemical-communication pathways to control invasive amphibians.
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spelling pubmed-72597512020-06-08 Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure McCann, Samantha Crossland, Michael Shine, Richard PLoS One Research Article Attempts to control invasive species using species-specific pheromones need to incorporate an understanding of interactive effects among those pathways. The larvae of invasive cane toads (Rhinella marina) utilise chemical cues to repulse, attract or suppress conspecific larvae. We can exploit these effects to reduce toad abundance, but the effects of each cue may not be additive. That is, exposure to one type of cue may lessen the impact of exposure to another cue. To assess this possibility, we exposed toad larvae to combinations of cues. Tadpoles that had been exposed to the suppression cue during larval development exhibited no response to the attraction cue, resulting in lower capture rates in attractant-baited traps. Suppression, however, did not affect a tadpole’s response to the alarm cue, and exposure to the alarm cue during tadpole development did not affect response to the attraction cue. Tadpoles exposed to the suppression cue were smaller than control tadpoles at 10 days post-exposure, and consequently were more vulnerable to gape-limited invertebrate predators. Our results demonstrate that the responses by toad tadpoles to chemical cues interact in important ways, and are not simply additive when combined. Control efforts need to incorporate an understanding of such interactions if we are to most effectively use chemical-communication pathways to control invasive amphibians. Public Library of Science 2020-05-29 /pmc/articles/PMC7259751/ /pubmed/32469938 http://dx.doi.org/10.1371/journal.pone.0233653 Text en © 2020 McCann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
McCann, Samantha
Crossland, Michael
Shine, Richard
Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
title Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
title_full Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
title_fullStr Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
title_full_unstemmed Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
title_short Exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
title_sort exposure of cane toad hatchlings to older conspecifics suppresses chemosensory food tracking behaviour and increases risk of predation post-exposure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259751/
https://www.ncbi.nlm.nih.gov/pubmed/32469938
http://dx.doi.org/10.1371/journal.pone.0233653
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