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2007
DOI: 10.1016/j.anbehav.2006.08.005
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Vocal signalling of male southern elephant seals is honest but imprecise

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Cited by 118 publications
(101 citation statements)
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References 40 publications
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“…(Dunn et al, 2015;Kelemen and Sade, 1960), and hammer-headed bats, Hypsignathus monstrosus (Bradbury, 1977); and even an additional, non-laryngeal set of vocal folds (termed 'velar vocal folds') in the koala, Phascolarctos cinereus (Charlton et al, 2013). Other species produce abnormally low formants for their size by extending their vocal tracts using descended and/or mobile larynges (red deer, Cervus elaphus, Reby and McComb, 2003;fallow deer, Dama dama, McElligott et al, 2006; Mongolian gazelle, Procapra gutturosa, Frey et al, 2008; goitred gazelle, Gazella subgutturosa, Frey et al, 2011;koala, Charlton et al, 2011; roaring cats, Panthera sp., Weissengruber et al, 2002), air sacs (black and white colobus monkey, Colobus guereza, Harris et al, 2006) and nasal proboscises (African elephant, Loxodonta africana, McComb et al, 2003;saiga, Saiga t. tatarica, Frey et al, 2007; elephant seals, Mirounga leonina, Sanvito et al, 2007). These anatomical adaptations are thought to evolve via selection pressures for individuals to lower frequency components, either to broadcast an exaggerated impression of their body size in reproductive contexts or to maximise signal propagation in the species' natural environment (koala, Charlton et al, 2011Charlton et al, , 2013red deer, Fitch and Reby, 2001;Reby and McComb, 2003;fallow deer, Vannoni and McElligott, 2008;bison, Bison bison, Wyman et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…(Dunn et al, 2015;Kelemen and Sade, 1960), and hammer-headed bats, Hypsignathus monstrosus (Bradbury, 1977); and even an additional, non-laryngeal set of vocal folds (termed 'velar vocal folds') in the koala, Phascolarctos cinereus (Charlton et al, 2013). Other species produce abnormally low formants for their size by extending their vocal tracts using descended and/or mobile larynges (red deer, Cervus elaphus, Reby and McComb, 2003;fallow deer, Dama dama, McElligott et al, 2006; Mongolian gazelle, Procapra gutturosa, Frey et al, 2008; goitred gazelle, Gazella subgutturosa, Frey et al, 2011;koala, Charlton et al, 2011; roaring cats, Panthera sp., Weissengruber et al, 2002), air sacs (black and white colobus monkey, Colobus guereza, Harris et al, 2006) and nasal proboscises (African elephant, Loxodonta africana, McComb et al, 2003;saiga, Saiga t. tatarica, Frey et al, 2007; elephant seals, Mirounga leonina, Sanvito et al, 2007). These anatomical adaptations are thought to evolve via selection pressures for individuals to lower frequency components, either to broadcast an exaggerated impression of their body size in reproductive contexts or to maximise signal propagation in the species' natural environment (koala, Charlton et al, 2011Charlton et al, , 2013red deer, Fitch and Reby, 2001;Reby and McComb, 2003;fallow deer, Vannoni and McElligott, 2008;bison, Bison bison, Wyman et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…Recent theoretical and technical advances in mammalian bioacoustics, centred around the application of the source-filter theory of voice production to voiced signals (Fant 1960;Fitch 2002), have enabled investigators to understand the acoustic structure of mammal vocal signals according to their modes of production, and to predict the covariation of specific acoustic features with physiological or morphological attributes of callers (Fitch 1997;Riede & Fitch 1999;Reby & McComb 2003a;Harris et al 2006;Sanvito et al 2007;Vannoni & McElligott 2008;Charlton et al 2009). The source filter theory states that vocal signals result from a two-stage production process, with the glottal wave generated in the larynx (the source), being subsequently filtered in the supra-laryngeal vocal tract (the filter ;Fant 1960;Titze 1994).…”
Section: Introductionmentioning
confidence: 99%
“…Several recent publications applying the source-filter framework to the study of mammal signals have shown that vocal tract resonances, which reflect the length and shape of the vocal tract, are reliable acoustic cues to body size (Fitch 1997;Riede & Fitch 1999;Reby & McComb 2003a;Harris et al 2006;Sanvito et al 2007;Vannoni & McElligott 2008;Charlton et al 2009) and identity (Rendall 2003;Kidjo et al 2008). By contrast, despite its dependence on the length, mass and tension of vocal folds (Titze 1994), in mammals the fundamental frequency of vocalizations does not consistently provide reliable information on body size (Lass & Brown 1978;Reby & McComb 2003a;Rendall et al 2005; but see Pfefferle & Fisher 2006).…”
Section: Introductionmentioning
confidence: 99%
“…The Auk: Ornithological Advances 135:44-59, Q 2018 American Ornithological Society always consistent and has been found to be weak or nonexistent in others species (Cardoso and Mota 2007, Sanvito et al 2007, Cardoso et al 2008, Peters et al 2009). Little Penguins settle disputes by using an ''escalation process'' in which individuals increase their aggressive behaviors-generally by increasing the intensity and amplitude of their calls, grading from agonistic to advertising calls-until one retreats (Waas 1991a(Waas , 2006.…”
Section: Discussionmentioning
confidence: 94%