1991
DOI: 10.1111/j.1439-0310.1991.tb00276.x
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Male Mate Choice in Mixed Bisexual/Unisexual Breeding Complexes of Poecilia (Teleostei: Poeciliidae)

Abstract: The livebearing all‐female fish Poecilia formosa reproduces by gynogenesis, a modified form of parthenogenesis. P. formosa forms at least two breeding complexes: in its northern range it exists sympatrically with Poecilia latipinna and in its southern range with Poecilia mexicana. Differences between these complexes and their possible origin are discussed. Embryogenesis is triggered by sperm of males of these closely related sympatric species. Because inheritance is strictly maternal, from the male point of vi… Show more

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Cited by 77 publications
(45 citation statements)
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“…This result is contrary to prior experiments that have evaluated the effect of visual cues on both male and female sailfin molly association preference for female conspecifics versus Amazon mollies (Schlupp et al 1991, Schlupp and Ryan 1996Gumm et al 2006). One hypothesis that warrants further consideration is that there is geographic variation in the ways that male sailfin mollies discriminate between species or in the ability to discriminate based on visual cues.…”
Section: Discussioncontrasting
confidence: 84%
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“…This result is contrary to prior experiments that have evaluated the effect of visual cues on both male and female sailfin molly association preference for female conspecifics versus Amazon mollies (Schlupp et al 1991, Schlupp and Ryan 1996Gumm et al 2006). One hypothesis that warrants further consideration is that there is geographic variation in the ways that male sailfin mollies discriminate between species or in the ability to discriminate based on visual cues.…”
Section: Discussioncontrasting
confidence: 84%
“…There is evidence of geographic variation in male sailfin molly mating preference (Gabor and Ryan 2001;Gumm and Gabor 2005). Therefore it is possible that the populations of males that we used in our studies differ behaviorally from the males from other populations used in the studies of Schlupp et al (1991), and Schlupp andRyan (1996, 1997) and Gumm et al (2006).…”
Section: Discussionmentioning
confidence: 86%
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“…Empirical data, however, show enormous temporal and spatial variation and plasticity in male mate discrimination ability D: male mate preference for sexual over asexual females varies seasonally in terms of association preference (Heubel and Schlupp 2008) and sperm transfer (Riesch et al 2008), and among populations depending on the species complex and the strength of sexual-asexual sympatry (Ryan et al 1996, Gabor andRyan 2001). Male mate discrimination may conflict with preferences for large body size (Gumm and Gabor 2005) or female receptivity (Schlupp et al 1991) and be weakened by social effects such as mate-copying (Schlupp and Ryan 1997) or presence of potential competitors ). This result is in good line with theoretical predictions that male mate choice, even if good for the species, may fail to become strong when based (a) 99% decline counts as extinction (b) 99.9% decline counts as extinction on individual-level selection (Schmeller et al 2005, Servedio andLande 2006).…”
Section: Population Consequences Of Male Mate Choicementioning
confidence: 97%
“…Secondly, distinguishing the two types of females may become very difficult for males because females may evolve counter-adaptations to avoid being discriminated against (Schlupp et al 1991, Lima et al 1996. Thirdly, male discrimination against asexual females may occasionally lead to loss of real reproductive opportunities through erroneous rejection of conspecifics (Schmeller et al 2005, Hochkirch et al 2007).…”
mentioning
confidence: 98%