dc.contributor.author | Lawrence, J. P. | |
dc.contributor.author | Rojas, Bibiana | |
dc.contributor.author | Fouquet, Antoine | |
dc.contributor.author | Mappes, Johanna | |
dc.contributor.author | Blanchette, Annelise | |
dc.contributor.author | Saporito, Ralph A. | |
dc.contributor.author | Bosque, Renan Janke | |
dc.contributor.author | Courtois, Elodie A. | |
dc.contributor.author | Noonan, Brice P. | |
dc.date.accessioned | 2019-09-20T06:57:21Z | |
dc.date.available | 2019-09-20T06:57:21Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Lawrence, J. P., Rojas, B., Fouquet, A., Mappes, J., Blanchette, A., Saporito, R. A., Bosque, R. J., Courtois, E. A., & Noonan, B. P. (2019). Weak warning signals can persist in the absence of gene flow. <i>Proceedings of the National Academy of Sciences of the United States of America</i>, <i>116</i>(38), 19037-19045. <a href="https://doi.org/10.1073/pnas.1901872116" target="_blank">https://doi.org/10.1073/pnas.1901872116</a> | |
dc.identifier.other | CONVID_32520571 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/65579 | |
dc.description.abstract | Aposematic organisms couple conspicuous warning signals with a secondary defense to deter predators from attacking. Novel signals of aposematic prey are expected to be selected against due to positive frequency-dependent selection. How, then, can novel phenotypes persist after they arise, and why do so many aposematic species exhibit intrapopulation signal variability? Using a polytypic poison frog (Dendrobates tinctorius), we explored the forces of selection on variable aposematic signals using 2 phenotypically distinct (white, yellow) populations. Contrary to expectations, local phenotype was not always better protected compared to novel phenotypes in either population; in the white population, the novel phenotype evoked greater avoidance in natural predators. Despite having a lower quantity of alkaloids, the skin extracts from yellow frogs provoked higher aversive reactions by birds than white frogs in the laboratory, although both populations differed from controls. Similarly, predators learned to avoid the yellow signal faster than the white signal, and generalized their learned avoidance of yellow but not white. We propose that signals that are easily learned and broadly generalized can protect rare, novel signals, and weak warning signals (i.e., signals with poor efficacy and/or poor defense) can persist when gene flow among populations, as in this case, is limited. This provides a mechanism for the persistence of intrapopulation aposematic variation, a likely precursor to polytypism and driver of speciation. | en |
dc.format.mimetype | application/pdf | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | National Academy of Sciences | |
dc.relation.ispartofseries | Proceedings of the National Academy of Sciences of the United States of America | |
dc.rights | CC BY-NC-ND 4.0 | |
dc.subject.other | aposematism | |
dc.subject.other | frequency-dependent selection | |
dc.subject.other | polymorphism | |
dc.subject.other | unpalatability | |
dc.subject.other | secondary defenses | |
dc.title | Weak warning signals can persist in the absence of gene flow | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-201909204226 | |
dc.contributor.laitos | Bio- ja ympäristötieteiden laitos | fi |
dc.contributor.laitos | Department of Biological and Environmental Science | en |
dc.contributor.oppiaine | Ekologia ja evoluutiobiologia | fi |
dc.contributor.oppiaine | Biologisten vuorovaikutusten huippututkimusyksikkö | fi |
dc.contributor.oppiaine | Ecology and Evolutionary Biology | en |
dc.contributor.oppiaine | Centre of Excellence in Biological Interactions Research | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 19037-19045 | |
dc.relation.issn | 0027-8424 | |
dc.relation.numberinseries | 38 | |
dc.relation.volume | 116 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © The Authors, 2019 | |
dc.rights.accesslevel | openAccess | fi |
dc.relation.grantnumber | 284666 | |
dc.subject.yso | varoitusväri | |
dc.subject.yso | luonnonvalinta | |
dc.subject.yso | puolustusmekanismit (biologia) | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p27907 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p4473 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p6078 | |
dc.rights.url | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.relation.dataset | https://doi.org/10.17011/jyx/dataset/65263 | |
dc.relation.doi | 10.1073/pnas.1901872116 | |
dc.relation.funder | Suomen Akatemia | fi |
dc.relation.funder | Research Council of Finland | en |
jyx.fundingprogram | Huippuyksikkörahoitus, SA | fi |
jyx.fundingprogram | Centre of Excellence, AoF | en |
jyx.fundinginformation | This work was supported in part by Investissement d’Avenir Grant CEBA ANR-10-LABX-25-01 of the Agence Nationale de la Recherche; the American Society of Ichthyologists and Herpetologists’ Gaige Award (to J.P.L.); and a Society for the Study of Amphibians and Reptiles’ grant in Herpetology (to J.P.L.). B.R. and J.M. were funded by the Finnish Centre of Excellence in Biological Interactions (Project 28466, to J.M.). B.R. also acknowledges funding from the Academy of Finland (Academy Research Fellowship, project No. 21000042021). | |
dc.type.okm | A1 | |