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dc.contributor.authorHämäläinen, Liisa
dc.contributor.authorMappes, Johanna
dc.contributor.authorRowland, Hannah M.
dc.contributor.authorThorogood, Rose
dc.date.accessioned2019-10-14T08:50:29Z
dc.date.available2019-10-14T08:50:29Z
dc.date.issued2019
dc.identifier.citationHämäläinen, L., Mappes, J., Rowland, H. M., & Thorogood, R. (2019). Social information use about novel aposematic prey is not influenced by a predator's previous experience with toxins. <i>Functional Ecology</i>, <i>33</i>(10), 1982-1992. <a href="https://doi.org/10.1111/1365-2435.13395" target="_blank">https://doi.org/10.1111/1365-2435.13395</a>
dc.identifier.otherCONVID_31254499
dc.identifier.otherTUTKAID_81828
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/65856
dc.description.abstractAposematism is an effective antipredator strategy. However, the initial evolution and maintenance of aposematism are paradoxical because conspicuous prey are vulnerable to attack by naïve predators. Consequently, the evolution of aposematic signal mimicry is also difficult to explain. The cost of conspicuousness can be reduced if predators learn about novel aposematic prey by observing another predator's response to that same prey. On the other hand, observing positive foraging events might also inform predators about the presence of undefended mimics, accelerating predation on both mimics and their defended models. It is currently unknown, however, how personal and social information combines to affect the fitness of aposematic prey. For example, does social information become more useful when predators have already ingested toxins and need to minimize further consumption? We investigated how toxin load influences great tits' (Parus major) likelihood to use social information about novel aposematic prey, and how it alters predation risk for undefended mimics. Birds were first provided with mealworms injected with bitter‐tasting chloroquine (or a water‐injected control), before information about a novel unpalatable prey phenotype was provided via video playback (either prey alone, or of a great tit tasting the noxious prey). An experimentally increased toxin load made great tits warier to attack prey, but only if they lacked social information about unpalatable prey. Socially educated birds consumed fewer aposematic prey relative to a cryptic phenotype, regardless of toxin load. In contrast, after personally experiencing aposematic prey, birds ignored social information about palatable mimics and were hesitant to sample them. Our results suggest that social information use by predators could be a powerful force in facilitating the evolution of aposematism as it reduces predation pressure on aposematic prey, regardless of a predator's toxin load. Nevertheless, observing foraging events of others is unlikely to alter frequency‐dependent dynamics among models and mimics, although this may depend on predators having recent personal experience of the model's unpalatability.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley-Blackwell Publishing Ltd.
dc.relation.ispartofseriesFunctional Ecology
dc.rightsCC BY 4.0
dc.subject.otheraposematism
dc.subject.othergreat tits
dc.subject.otherpredator-prey interactions
dc.subject.othertoxin load
dc.titleSocial information use about novel aposematic prey is not influenced by a predator's previous experience with toxins
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201910084365
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.oppiaineEkologia ja evoluutiobiologiafi
dc.contributor.oppiaineEcology and Evolutionary Biologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2019-10-08T12:15:16Z
dc.description.reviewstatuspeerReviewed
dc.format.pagerange1982-1992
dc.relation.issn0269-8463
dc.relation.numberinseries10
dc.relation.volume33
dc.type.versionpublishedVersion
dc.rights.copyright© 2019 The Authors.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber284666
dc.subject.ysomimikry
dc.subject.ysososiaalinen oppiminen
dc.subject.ysopetoeläimet
dc.subject.ysosaaliseläimet
dc.subject.ysotoksiinit
dc.subject.ysosuojaväri
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p29065
jyx.subject.urihttp://www.yso.fi/onto/yso/p16193
jyx.subject.urihttp://www.yso.fi/onto/yso/p14567
jyx.subject.urihttp://www.yso.fi/onto/yso/p28137
jyx.subject.urihttp://www.yso.fi/onto/yso/p10863
jyx.subject.urihttp://www.yso.fi/onto/yso/p27847
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1111/1365-2435.13395
dc.relation.funderSuomen Akatemiafi
dc.relation.funderAcademy of Finlanden
jyx.fundingprogramHuippuyksikkörahoitus, SAfi
jyx.fundingprogramCentre of Excellence, AoFen
jyx.fundinginformationWe are grateful to Tuuli Salmi for helping with the experiment, Helinä Nisu for taking care of the birds, staff at the Konnevesi Research Station for providing facilities for the experiments and Victoria Franks for providing illustrations. LH was funded by the Finnish Cultural Foundation and Emil Aaltonen Foundation. RT was supported by an Independent Research Fellowship from the Natural Environment Research Council UK (NE/K00929X/1) and a start‐up grant from the Helsinki Institute of Life Science (HiLIFE), University of Helsinki. HMR was supported by a research fellowship from the Institute of Zoology and is currently supported by the Max Plank Society. JM was supported by the Academy of Finland via the Finnish Centre of Excellence Program and the University of Jyväskylä which also offered facilities for the experiments. Wild birds were used with permission from the Central Finland Centre for Economic Development, Transport and Environment and licence from the National Animal Experiment Board (ESAVI/9114/04.10.07/2014) and the Central Finland Regional Environmental Centre (VARELY/294/2015).


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