Näytä suppeat kuvailutiedot

dc.contributor.authorKervinen, Matti
dc.contributor.authorLebigre, Christophe
dc.contributor.authorSoulsbury, Carl D.
dc.date.accessioned2016-08-24T09:50:04Z
dc.date.available2016-08-24T09:50:04Z
dc.date.issued2016
dc.identifier.citationKervinen, M., Lebigre, C., & Soulsbury, C. D. (2016). Simultaneous age-dependent and age-independent sexual selection in the lekking black grouse (Lyrurus tetrix). <i>Journal of Animal Ecology</i>, <i>85</i>(3), 715-725. <a href="https://doi.org/10.1111/1365-2656.12496" target="_blank">https://doi.org/10.1111/1365-2656.12496</a>
dc.identifier.otherCONVID_25582739
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/51044
dc.description.abstractIndividuals' reproductive success is often strongly associated with their age, with typical patterns of early‐life reproductive improvement and late‐life senescence. These age‐related patterns are due to the inherent trade‐offs between life‐history traits competing for a limited amount of resources available to the organisms. In males, such trade‐offs are exacerbated by the resource requirements associated with the expression of costly sexual traits, leading to dynamic changes in trait expression throughout their life span. Due to the age dependency of male phenotypes, the relationship between the expression of male traits and mating success can also vary with male age. Hence, using longitudinal data in a lekking species with strong sexual selection – the black grouse Lyrurus tetrix – we quantified the effects of age, life span and age of first lek attendance (AFL) on male annual mating success (AMS) to separate the effects of within‐individual improvement and senescence on AMS from selective (dis)appearance of certain phenotypes. Then, we used male AMS to quantify univariate and multivariate sexual selection gradients on male morphological and behavioural traits with and without accounting for age and age‐related effects of other traits. Male AMS increased with age, and there was no significant reproductive senescence. Most males never copulated, and of the ones that did, the majority had only one successful year. Life span was unrelated to AMS, but early AFL tended to lead to higher AMS at ages 1–3. AMS was related to most morphological and behavioural traits when male age was ignored. Accounting for age and age‐specific trait effects (i.e. the interaction between a trait and age) reduced the magnitude of the selection gradients and revealed that behavioural traits are under consistent sexual selection, while sexual selection on morphological traits is stronger in old males. Therefore, sexual selection in black grouse operates primarily on male behaviour and morphological traits may act as additional cues to supplement female choice. These results demonstrate the multifaceted influence of age on both fitness and sexual traits and highlight the importance of accounting for such effects when quantifying sexual selection.en
dc.language.isoeng
dc.publisherWiley-Blackwell Publishing Ltd.; British Ecological Society
dc.relation.ispartofseriesJournal of Animal Ecology
dc.subject.otherannual reproductive success
dc.subject.otherfitness
dc.subject.otherlek
dc.subject.otherlong-term data
dc.subject.othermating success
dc.subject.otherselection differential
dc.subject.otherselection gradient
dc.subject.othersenescence
dc.subject.otherTetrao tetrix
dc.titleSimultaneous age-dependent and age-independent sexual selection in the lekking black grouse (Lyrurus tetrix)
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-201607253661
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.updated2016-07-25T09:15:10Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange715-725
dc.relation.issn0021-8790
dc.relation.numberinseries3
dc.relation.volume85
dc.type.versionpublishedVersion
dc.rights.copyright© 2016 The Authors Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. This is an open access article under the terms of the Creative Commons Attribution License.
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.datasethttp://dx.doi.org/10.5061/dryad.2jj6q
dc.relation.doi10.1111/1365-2656.12496
jyx.fundinginformationThis study was funded by the Center of Excellence in Evolutionary Research in University of Jyväskylä (project no. 7211271 to R.V.A.), the Academy of Finland (project no. 7119165 to H.S.) and the Emil Aaltonen Foundation (personal grant to M.K.). Birds were captured under the permissions of the Central Finland Environmental Centre (permissions KSU‐2003‐L‐25/254 and KSU‐2002‐L‐4/254).
dc.type.okmA1


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Näytä suppeat kuvailutiedot

© 2016 The Authors Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. This is an open access article under the terms of the Creative Commons Attribution License.
Ellei muuten mainita, aineiston lisenssi on © 2016 The Authors Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. This is an open access article under the terms of the Creative Commons Attribution License.