1992
DOI: 10.1016/s0003-3472(05)80074-0
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Wing melanin pattern mediates species recognition in Pieris occidentalis

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Cited by 57 publications
(40 citation statements)
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“…At the same time, the ventral eyespot appears to have no role in sexual communication, in contrast to the clear role of the dorsal, and non-plastic, eyespot in mate choice ( Robertson & Monteiro, 2005 ). However, North American P. rapae are sexually monomorphic in UV reflectance ( Scott, 1986 ), so melanisation may be important in male and/or female mate choice and species recognition, as is the case in other pierids ( Wiernasz, 1989( Wiernasz, , 1995Wiernasz & Kingsolver, 1992;Ellers & Boggs, 2003 ). In Japanese populations of P. rapae , sexual dimorphism in ultraviolet (UV) reflectance of the non-melanised portions of the wings appears to be more important in sexual communication than the black pattern elements ( Obara, 1970 ).…”
Section: Discussionmentioning
confidence: 99%
“…At the same time, the ventral eyespot appears to have no role in sexual communication, in contrast to the clear role of the dorsal, and non-plastic, eyespot in mate choice ( Robertson & Monteiro, 2005 ). However, North American P. rapae are sexually monomorphic in UV reflectance ( Scott, 1986 ), so melanisation may be important in male and/or female mate choice and species recognition, as is the case in other pierids ( Wiernasz, 1989( Wiernasz, , 1995Wiernasz & Kingsolver, 1992;Ellers & Boggs, 2003 ). In Japanese populations of P. rapae , sexual dimorphism in ultraviolet (UV) reflectance of the non-melanised portions of the wings appears to be more important in sexual communication than the black pattern elements ( Obara, 1970 ).…”
Section: Discussionmentioning
confidence: 99%
“…Divergence in mate choice preferences can occur between populations that become geographically isolated (allopatric reproductive isolation), leading to the persistence of reproductive isolation following secondary contact between the populations (sympatric reproductive isolation). Examples of signals that have contributed to behavioural isolation involve visual signals observed in butterflies (Wiernasz and Kingsolver, 1992), damselflies (Saetre et al, 1997), fish (Seehausen and Van Alphen, 1998) and frogs (Maan and Cummings, 2008), acoustic signals observed in insects, frogs (Gerhardt and Huber, 2002) and bats (Barlew and Jones, 1997), and chemical signals observed in moths (Linn and Roelofs, 1995), spiders (Trabalon et al, 1997), and flies (Coyne et al, 1994). Variation in these signals between lineages can result in pre-mating reproductive isolation, providing a behavioural mechanism driving speciation (Smadja and Butlin, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…Theory predicts that divergence in these mating signals, coupled with coevolution of female preferences, can lead to speciation (Lande, 1981) and reproductive isolation upon secondary contact (Uyeda et al, 2009). For example, wing colour and pattern facilitate behavioural isolation in butterflies (Wiernasz & Kingsolver, 1992;Jiggins et al, 2001Jiggins et al, , 2004Melo et al, 2009). Male colour differences are also known to contribute to assortative mating in fishes as well (Seehausen & van Alphen, 1998;Williams & Mendelson, 2010.…”
Section: Introductionmentioning
confidence: 99%