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Evolution of sex-specific pace-of-life syndromes: causes and consequences

  • Anni Hämäläinen
  • Elina Immonen
  • Maja Tarka
  • Wiebke Schuett
Review
Part of the following topical collections:
  1. Pace-of-life syndromes: a framework for the adaptive integration of behaviour, physiology and life-history

Abstract

Males and females commonly differ in their life history optima and, consequently, in the optimal expression of life history, behavioral and physiological traits involved in pace-of-life syndromes (POLS). Sex differences in mean trait expression typically result if males and females exhibit different fitness optima along the same pace-of-life continuum, but the syndrome structure may also differ for the sexes. Due to sex-specific selective pressures imposed by reproductive roles and breeding strategies, the sexes may come to differ in the strength of correlation among traits, or different traits may covary in males and females. Ignorance of these selective forces operating between and within the sexes may lead to flawed conclusions about POLS manifestation in the species, and stand in the way of understanding the evolution, maintenance, and variability of POLS. We outline ways in which natural and sexual selection influence sex-specific trait evolution, and describe potential ultimate mechanisms underlying sex-specific POLS. We make predictions on how reproductive roles and the underlying sexual conflict lead to sex-specific trait covariances. These predictions lead us to conclude that sexual dimorphism in POLS is expected to be highly prevalent, allow us to assess possible consequences for POLS evolution, and provide guidelines for future studies.

Keywords

Integrated phenotype Life history Mating system Personality POLS Sexual dimorphism 

Notes

Acknowledgments

We thank the guest editors Niels Dingemanse, Melanie Dammhahn, Petri Niemelä, and Denis Réale for organizing the POLS workshops and this Topical Collection, the VW Foundation for funding the workshops, and all workshop participants for fruitful discussions. Insightful feedback from the guest editors, David Fisher, and anonymous reviewers helped improve the paper. We acknowledge financial support from Research Council of Norway (SFF-III 223257) to MT, European Research Council (AdG-294333, grant to Göran Arnqvist) to EI, and the Alberta Biodiversity Conservation Chair to AH.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary material

265_2018_2466_MOESM1_ESM.docx (127 kb)
ESM 1 (DOCX 126 kb)

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Authors and Affiliations

  1. 1.Department of Biological SciencesUniversity of AlbertaEdmontonCanada
  2. 2.Department of Ecology and Genetics, Evolutionary Biology CentreUppsala UniversityUppsalaSweden
  3. 3.Centre for Biodiversity Dynamics, Department of BiologyNorwegian University of Science and Technology (NTNU)TrondheimNorway
  4. 4.Zoological InstituteUniversity of HamburgHamburgGermany

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