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(a) Principle component analysis of allele frequency variation for all loci in 12 populations of Poecilia latipinna. Open circles are sympatric populations, filled circles, are allopatric populations. (b) Results of multidimensional scaling analyses, displayed as pairwise two dimensional scatterplots using dimension one vs dimension two. (c) MDS of dimension one vs. dimension three. The first two dimensions account for most of the differentiation and the first three dimensions account for virtually all of the differentiation. Population designations are the same as in Figure 1.  

(a) Principle component analysis of allele frequency variation for all loci in 12 populations of Poecilia latipinna. Open circles are sympatric populations, filled circles, are allopatric populations. (b) Results of multidimensional scaling analyses, displayed as pairwise two dimensional scatterplots using dimension one vs dimension two. (c) MDS of dimension one vs. dimension three. The first two dimensions account for most of the differentiation and the first three dimensions account for virtually all of the differentiation. Population designations are the same as in Figure 1.  

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We analyzed variation in allozymes and mating preferences in 12 populations across much of the range of the sailfin molly, Poecilia latipinna. Sailfin mollies can be sympatric with its sexual parasite Amazon mollies, P. formosa. Amazon mollies must co-exist and mate with bisexual males of closely related species (including sailfin mollies) to induc...

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... Previous attempts to cross the parental species are not informative here, because they were set up as forced crosses of one or several unmated (virgin) female(s) and one or several males, leaving little opportunity for females to exercise mate choice. In general, mate choice in this system has been addressed widely (Schlupp, 2005(Schlupp, , 2009(Schlupp, , 2018, including character displacement in males (Gabor et al., 2005;Gabor & Ryan, 2001). Many hypotheses exist that can explain female preferences, including an almost universal preference for larger males size (Ryan & Keddy-Hector, 1992), but in the context of this study, the idea of a preexisting bias governing mate preferences of female mollies, in particular females of species with short dorsal fins (Ptacek, 1998) because males are more ornamented, seems particularly relevant (Endler & Basolo, 1998;Ryan, 1990) (Figure 1). ...
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... While only a few studies examined geographical variation in male mate choice against asexuals, some empirical support for such hypothesis exists. For instance, Gabor and Ryan (2001) and Gabor et al. (2005) found that males of the sexual sailfin molly (P. latipinna) living sympatrically with gynogenetic Amazon mollies (P. ...
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... The fact that females generally appear to be the choosiest sex in most animals may give rise to a bias in evolutionary research [9]. However some recent studies mentioned the occurrence of RCD in male mate preferences [10][11][12][13]. Occurrence of male mate choice in species from different taxa (actinopterygians, birds, insects, mammals) and contribution of female sexual traits and male choosiness to specific reproductive isolation [14,15] may indicate that this phenomenon is more common than previously thought. ...
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