2018
DOI: 10.1111/1365-2656.12855
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From ornament to armament or loss of function? Breeding plumage acquisition in a genetically monogamous bird

Abstract: The evolution of conspicuous male traits is thought to be driven by female mate choice or male-male competition. These two mechanisms are often viewed as distinct processes, with most studies focusing on female choice. However, both mechanisms of sexual selection can act simultaneously on the same trait (i.e., dual function) and/or interact in a synergistic or conflicting way. Dual-function traits are commonly assumed to originate through male-male competition before being used in female choice; yet, most stud… Show more

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Cited by 15 publications
(11 citation statements)
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“…An example for these processes is found in Malurus fairy‐wrens. Seasonal plumage colours have been lost in two species, the lovely and white‐shouldered fairy‐wrens ( M. amabilis and M. alboscapulatus; Fan et al ). Both species have high annual survival rates (Leitão et al ) and live in the tropics, where predation risk on fairy‐wrens appears to be relatively low (Cain et al ) and where reduced seasonality may favour less well‐defined breeding schedules (Leitão et al ).…”
Section: Discussionmentioning
confidence: 99%
“…An example for these processes is found in Malurus fairy‐wrens. Seasonal plumage colours have been lost in two species, the lovely and white‐shouldered fairy‐wrens ( M. amabilis and M. alboscapulatus; Fan et al ). Both species have high annual survival rates (Leitão et al ) and live in the tropics, where predation risk on fairy‐wrens appears to be relatively low (Cain et al ) and where reduced seasonality may favour less well‐defined breeding schedules (Leitão et al ).…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, the combination of behavioral observations with ancestral state reconstructions should help fill in the gaps for phylogenies in which some species are known to use dual‐utility traits, and in which other species may have lost the trait function for courtship, as in Malurus fairy wrens (Fan et al. ).…”
Section: Discussionmentioning
confidence: 99%
“…Dual-utility displays have been found in members of several species-rich groups, such as auks (Jones and Hunter 1999), widowbirds (Andersson et al 2002), Old World sparrows (Griggio et al 2007), antbirds (Tobias et al 2011), darter fish (Zhou and Fuller 2016), and deer (Morina et al 2018); and phylogenetic analyses of ornamentation in speciose clades (such as poeciliids) can provide a greater picture of the processes by which trait co-option has occurred. Furthermore, the combination of behavioral observations with ancestral state reconstructions should help fill in the gaps for phylogenies in which some species are known to use dual-utility traits, and in which other species may have lost the trait function for courtship, as in Malurus fairy wrens (Fan et al 2018).…”
Section: Aggression and Courtshipmentioning
confidence: 99%
“…PCFWs were sampled at multiple time periods over their lives [ n = 105 nestlings 7 days old, free-flying birds ranging from age 1–139 months (1st year, n = 516; 2nd year, n = 134; 3rd year, n = 68; >4th year, n = 91)]. Sex was identified by plumage characteristics or molecular based techniques (Griffiths et al, 1998, Fan et al, 2018).
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Section: Methodsmentioning
confidence: 99%