2016
DOI: 10.1098/rspb.2016.1972
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Multivariate female preference tests reveal latent perceptual biases

Abstract: The question of why males of many species produce elaborate mating displays has now been largely resolved: females prefer to mate with males that produce such displays. However, the question of why females prefer such displays has been controversial, with an emerging consensus that such displays often provide information to females about the direct fitness benefits that males provide to females and/or the indirect fitness benefits provided to offspring. Alternative explanations, such as production of arbitrari… Show more

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Cited by 23 publications
(19 citation statements)
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“…Preexisting preference for a novel secondary sex characteristic has been described in other insects (Gray et al. ). With respect to differences in female CHCs, the evolution of the precise enzymes involved in the divergence of female‐specific 7,11‐HD expression is well described (Chertemps et al.…”
Section: Discussionmentioning
confidence: 84%
See 1 more Smart Citation
“…Preexisting preference for a novel secondary sex characteristic has been described in other insects (Gray et al. ). With respect to differences in female CHCs, the evolution of the precise enzymes involved in the divergence of female‐specific 7,11‐HD expression is well described (Chertemps et al.…”
Section: Discussionmentioning
confidence: 84%
“…Upon secondary contact, females of one species evolve a novel signal that exploits these preexisting biases, thereby minimizing the female costs associated with heterospecific courtship and/or mating. Preexisting preference for a novel secondary sex characteristic has been described in other insects (Gray et al 2016). With respect to differences in female CHCs, the evolution of the precise enzymes involved in the divergence of female-specific 7,11-HD expression is well described (Chertemps et al 2006;Chertemps et al 2007), with one enzyme in particular, desatF, showing a dynamic evolutionary history of gains and losses (Shirangi et al 2009).…”
Section: Role In Reproductive Isolationmentioning
confidence: 93%
“…The model thus provides testable hypotheses for how response properties in the neuronal network may have evolved to compute the preference functions of different species. For instance, species that prefer either shorter or longer pulse periods than G. bimaculatus like Teleogryllus leo (Rothbart and Hennig, 2012a), G. locorojo (Rothbart and Hennig, 2012b), G. firmus (Gray et al, 2016), or T. oceanicus (Hennig, 2003) could differ in the delays of inputs to LN3 (Fig. 5B).…”
Section: How To Tune a Cricket Song Detector?mentioning
confidence: 99%
“…The diverse song preferences have been extensively mapped in multiple species (e.g. (Bailey et al, 2017;Cros and Hedwig, 2014;Gray et al, 2016;Hennig, 2003;2009;Hennig et al, 2016;Rothbart and Hennig, 2012a;2012b)) and the song recognition network for one particular species is known . The computation performed by this system -the evaluation of a repetitive pulse pattern -is a common denominator of many communication systems from insects to fish and frogs (Baker et al, 2019;Carlson and Gallant, 2013;Gerhardt and Huber, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Too narrow a range may underestimate the amount of variation in the attractiveness of displaysit may not capture the full shape of the preference, which might yield misleading expectations about the form of sexual selection due to mate choice. On the other hand, an excessively broad range may detract from biological interpretability, although even then it might reveal hidden preferences or supernormal responses (Arak & Enquist, 1993;Gray et al, 2016). This is a decision that researchers have to make according to the biology of their study species and the scope of their research questions.…”
Section: The Assay Of Attractivenessmentioning
confidence: 99%