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Abstract
Vocalizations differ substantially between the sexes in many primates, and low-frequency male vocalizations may be favored by sexual selection because they intimidate rivals and/or attract mates. Sexual dimorphism in fundamental frequency may be more pronounced in species with more intense male mating competition and in those with large group size, where social knowledge is limited and efficient judgment of potential mates and competitors is crucial. These non-mutually exclusive explanations have not been tested simultaneously across primate species. In a sample of vocalizations (n = 1914 recordings) across 37 anthropoid species, we investigated whether fundamental frequency dimorphism evolved in association with increased intensity of mating competition (H1), large group size (H2), multilevel social organization (H3), a trade-off against the intensity of sperm competition (H4), and/or poor acoustic habitats (H5), controlling for phylogeny and body size dimorphism. We show that fundamental frequency dimorphism increased in evolutionary transitions towards larger group size and polygyny. Findings suggest that low-frequency male vocalizations in primates may have been driven by selection to win mating opportunities by avoiding costly fights and may be more important in larger groups, where limited social knowledge affords advantages to rapid assessment of status and threat potential via conspicuous secondary sexual characteristics.
Sexual dimorphism in the fundamental frequency of primate vocalizations is variable. Here, the authors examine 1914 vocalizations from 37 anthropoid species to find that fundamental frequency dimorphism increased with larger group size and polygyny, due to sexual selection.
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1 Pennsylvania State University, Department of Anthropology, University Park, USA (GRID:grid.29857.31) (ISNI:0000 0001 2097 4281); Immaculata University, Psychology and Counseling Department, Immaculata, USA (GRID:grid.257324.5) (ISNI:0000 0000 9817 2548)
2 University of Washington, Department of Anthropology, Seattle, USA (GRID:grid.34477.33) (ISNI:0000000122986657)
3 Welfare and Cognition Group, Cognitive Neuroscience Laboratory, German Primate Center – Leibniz Institute for Primate Research, Goettingen, Germany & Leibniz-ScienceCampus Primate Cognition, German Primate Center & University of Goettingen, Goettingen, Germany (GRID:grid.418215.b) (ISNI:0000 0000 8502 7018)
4 Max Planck Institute of Animal Behavior, Department for the Ecology of Animal Societies, Konstanz, Germany (GRID:grid.507516.0) (ISNI:0000 0004 7661 536X)
5 Columbia University, Department of Ecology, Evolution, and Environmental Biology, New York, USA (GRID:grid.21729.3f) (ISNI:0000000419368729)
6 Durham University, Department of Anthropology, Durham, UK (GRID:grid.8250.f) (ISNI:0000 0000 8700 0572)
7 Department of Anthropology, New York University, New York, USA (GRID:grid.137628.9) (ISNI:0000 0004 1936 8753)
8 IRD (French National Research Institute for Sustainable Development), Montpellier, France (GRID:grid.4399.7) (ISNI:0000000122879528)
9 University of Warwick, Department of Psychology, Coventry, UK (GRID:grid.7372.1) (ISNI:0000 0000 8809 1613)
10 University of Pennsylvania, Department of Psychology, Philadelphia, USA (GRID:grid.25879.31) (ISNI:0000 0004 1936 8972)
11 University of Florence, Sesto Fiorentino, Department of Biology, Florence, Italy (GRID:grid.8404.8) (ISNI:0000 0004 1757 2304)
12 California State Polytechnic University Humboldt, Department of Anthropology, Arcata, USA (GRID:grid.8404.8)
13 Universidad Nacional Autonoma de Mexico, Mexico, Institute for Research on Applied Mathematics and Systems and C3-Centro de Ciencias de la Complejidad, Mexico City, Mexico (GRID:grid.9486.3) (ISNI:0000 0001 2159 0001)
14 Pennsylvania State University, Department of Anthropology, University Park, USA (GRID:grid.29857.31) (ISNI:0000 0001 2097 4281)