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      Sex differences in age‐to‐maturation relate to sexual selection and adult sex ratios in birds

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          Abstract

          Maturation (the age when organisms are physiologically capable of breeding) is one of the major life history traits that have pervasive implications for reproductive strategies, fitness, and population growth. Sex differences in maturation are common in nature, although the causes of such differences are not understood. Fisher and Lack proposed that delayed maturation in males is expected when males are under intense sexual selection, but their proposition has never been tested across a wide range of taxa. By using phylogenetic comparative analyses and the most comprehensive dataset to date, including 201 species from 59 avian families, we show that intense sexual selection on males (as indicated by polygamous mating and male‐skewed sexual size dimorphism) correlates with delayed maturation. We also show that the adult sex ratio (ASR), an indicator of the social environment, is associated with sex‐specific maturation because in species with a female‐skewed ASR, males experience later maturation. Phylogenetic path analyses suggest that adult sex ratio drives interspecific changes in the intensity of sexual selection which, in turn, influences maturation. These results are robust to alternative phylogenetic hypotheses and to potential life‐history confounds, and they provide the first comprehensive support of Fisher's and Lack's propositions. Importantly, our work suggests that both social environment and mate competition influence the evolution of a major life history trait, maturation.

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          Most cited references37

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          Inferring evolutionary processes from phylogenies

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            Sexual selection in males and females.

            Research on sexual selection shows that the evolution of secondary sexual characters in males and the distribution of sex differences are more complex than was initially suggested but does not undermine our understanding of the evolutionary mechanisms involved. However, the operation of sexual selection in females has still received relatively little attention. Recent studies show that both intrasexual competition between females and male choice of mating partners are common, leading to strong sexual selection in females and, in extreme cases, to reversals in the usual pattern of sex differences in behavior and morphology.
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              Timing of pubertal maturation in girls: an integrated life history approach.

              Life history theory provides a metatheoretical framework for the study of pubertal timing from an evolutionary-developmental perspective. The current article reviews 5 middle-level theories--energetics theory, stress-suppression theory, psychosocial acceleration theory, paternal investment theory, and child development theory--each of which applies the basic assumptions of life history theory to the question of environmental influences on timing of puberty in girls. These theories converge in their conceptualization of pubertal timing as responsive to ecological conditions but diverge in their conceptualization of (a) the nature, extent, and direction of environmental influences and (b) the effects of pubertal timing on other reproductive variables. Competing hypotheses derived from the 5 perspectives are evaluated. An extension of W. T. Boyce and B. J. Ellis's (in press) theory of stress reactivity is proposed to account for both inhibiting and accelerating effects of psychosocial stress on timing of pubertal development. This review highlights the multiplicity of (often unrecognized) perspectives guiding research, raises challenges to virtually all of these, and presents an alternative framework in an effort to move research forward in this arena of multidisciplinary inquiry.
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                Author and article information

                Contributors
                sergio.ancona@iecologia.unam.mx
                Journal
                Evol Lett
                Evol Lett
                10.1002/(ISSN)2056-3744
                EVL3
                Evolution Letters
                John Wiley and Sons Inc. (Hoboken )
                2056-3744
                13 January 2020
                February 2020
                : 4
                : 1 ( doiID: 10.1002/evl3.v4.1 )
                : 44-53
                Affiliations
                [ 1 ] Departamento de Ecología Evolutiva, Instituto de Ecología Universidad Nacional Autónoma de México Ciudad de México 04510 México
                [ 2 ] MTA‐PE Evolutionary Ecology Research Group University of Pannonia PO Box 158 Veszprém 8201 Hungary
                [ 3 ] Department of Limnology University of Pannonia PO Box 158 Veszprém 8201 Hungary
                [ 4 ] Milner Centre for Evolution, Department of Biology & Biochemistry University of Bath Bath BA2 7AY UK
                [ 5 ] Department of Evolutionary Zoology and Human Biology University of Debrecen H‐4010 Debrecen Egyetem tér 1 Hungary
                Author notes
                Author information
                https://orcid.org/0000-0003-4595-1953
                https://orcid.org/0000-0002-7891-2312
                Article
                EVL3156
                10.1002/evl3.156
                7006465
                32055410
                f319f8eb-f0ad-487a-9ad4-3b6790cf8692
                © 2020 The Authors. Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB).

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 June 2019
                : 06 December 2019
                : 11 December 2019
                Page count
                Figures: 3, Tables: 1, Pages: 10, Words: 7741
                Funding
                Funded by: Hungarian Scientific Research Fund , open-funder-registry 10.13039/501100003549;
                Award ID: 20385‐3/2018/FEKUSTRAT
                Award ID: ELVONAL KKP‐126949
                Award ID: NKFIH 116310
                Award ID: NKFIH 130430
                Funded by: Consejo Nacional de Ciencia y Tecnología , open-funder-registry 10.13039/501100003141;
                Award ID: 216052
                Award ID: 311485
                Funded by: Royal Society Wolfson Merit Award
                Funded by: Natural Environment Research Fund (NERC)
                Award ID: NE/L002434/1
                Categories
                Letter
                Letters
                Custom metadata
                2.0
                February 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.5 mode:remove_FC converted:07.02.2020

                adult sex ratio,age at maturation,life histories,phylogenetic path analyses,sexual dimorphism,sexual selection

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