1993
DOI: 10.1038/hdy.1993.134
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The local displacement of a sexually reproducing ostracod by a conspecific parthenogen

Abstract: Candonocypris novaezelandiae is a freshwater ostracod which can perhaps best be described as a species complex of sexual and parthenogenetic forms of each of two morphs. Genetically distinct sexual and parthenogenetic forms of one of these morphs (the small-brown morph) coexist in a large maar lake in south-eastern Australia. Repeated sampling has revealed that the sex ratio of the small-brown morph in this lake is highly significantly biased in favour of females and that, during a 27 month sampling period, th… Show more

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Cited by 28 publications
(22 citation statements)
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“…But, in geographic parthenogens, the spatial distribution of sexual and asexual forms is disjointed by definition (Bell 1982;Suomalainen et al 1987;Schwander & Crespi 2009). In southeastern Australia, recent and rapid expansion of parthenogenetic females resulted in the local displacement of sexual lineages of Candonocypris novaezelandiae (Chaplin 1993;Chaplin & Ayre 1997). In H. barbara we have not found significant differences in life history traits between sexual and asexual females that coexist in Lampedusa Island temporary ponds (Rossi et al 2007).…”
Section: Discussionmentioning
confidence: 56%
“…But, in geographic parthenogens, the spatial distribution of sexual and asexual forms is disjointed by definition (Bell 1982;Suomalainen et al 1987;Schwander & Crespi 2009). In southeastern Australia, recent and rapid expansion of parthenogenetic females resulted in the local displacement of sexual lineages of Candonocypris novaezelandiae (Chaplin 1993;Chaplin & Ayre 1997). In H. barbara we have not found significant differences in life history traits between sexual and asexual females that coexist in Lampedusa Island temporary ponds (Rossi et al 2007).…”
Section: Discussionmentioning
confidence: 56%
“…By direct comparison we have observed that both female morphotypes from Lampedusa share several alíeles at different loci with winter clones of H. incongrunes from northern Italy (Rossi et al, 1996). In this case, our data should provide a further genetic evidence of coexisting syngamic and clonal lineages in ostracods as shown for Candonocypris novaezelandiae (Chaplin, 1992(Chaplin, , 1993Chaplin & Ayre, 1997) and Eucypris virens (Rossi et al, 1998;Schön et al, 2000;Rossi et al, in preparation).…”
Section: Locusmentioning
confidence: 86%
“…In geographic parthenogenetic species, such as H. incongruens, gene pool diversity among populations may be very high due to a wide geographic spread, fragmented habitat, low gene flow and high likelihood of bottlenecks. Among different clonal lineages of H. incongruens from the Po Plain, genetic similarity index ranged from 0.46 to 0.99 and was linked to morphological features and ecological specialisation (Rossi & Menozzi, 1990, 1993Rossi et al, 1993Rossi et al, , 1996. By direct comparison we have observed that both female morphotypes from Lampedusa share several alíeles at different loci with winter clones of H. incongrunes from northern Italy (Rossi et al, 1996).…”
Section: Locusmentioning
confidence: 87%
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“…Past breeding system determinations have relied on gender ratio analyses, with parthenogenesis being inferred for all-female populations. Genetic studies have now established the general validity of breeding system assignments made using the approach (Havel & Hebert, 1989), as the presence of males, even at low frequency, has always been associated with sexual recruitment (Chaplin, 1993).…”
mentioning
confidence: 99%