2002
DOI: 10.1016/s0169-5347(01)02331-x
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Ecology and evolution of sex in aphids

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Cited by 329 publications
(347 citation statements)
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“…Information on the diapause ability and ecological tolerance of eggs produced by females from these two families is not readily available (ie Forneck et al, 2001;Granett et al, 2001;Salom et al, 2001). Still, compared to their viviparous relatives, it is less likely that developmental constraints restrict the evolution of a coldresistant parthenogenetic egg (Rispe and Pierre, 1998;Simon et al, 2002). Possible overwintering asexually produced eggs have been observed on the stems of grapevines in a leaf feeding population of grape phylloxera in Arizona (Kimberling and Price, 1996).…”
Section: Discussionmentioning
confidence: 99%
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“…Information on the diapause ability and ecological tolerance of eggs produced by females from these two families is not readily available (ie Forneck et al, 2001;Granett et al, 2001;Salom et al, 2001). Still, compared to their viviparous relatives, it is less likely that developmental constraints restrict the evolution of a coldresistant parthenogenetic egg (Rispe and Pierre, 1998;Simon et al, 2002). Possible overwintering asexually produced eggs have been observed on the stems of grapevines in a leaf feeding population of grape phylloxera in Arizona (Kimberling and Price, 1996).…”
Section: Discussionmentioning
confidence: 99%
“…Many other life cycle variants have been described in members of the closely related Aphididae family, including the shift of cyclic parthenogenesis to functional/obligate parthenogenetic reproduction (Delmotte et al, 2001;Simon et al, 2002). Codominant molecular markers, such as microsatellites and allozymes, are extensively used to elucidate such modes of reproduction in this family (Sunnucks et al, 1996;Fuller et al, 1999;Wilson et al, 1999Wilson et al, , 2002Haack et al, 2000;Delmotte et al, 2001Delmotte et al, , 2002.…”
Section: Introductionmentioning
confidence: 99%
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“…This aphid has a range of lifecycle types, all of which reproduce parthenogenetically for most of the year, but which may or may not have an annual sexual phase (Dixon, 1998). These lifecycles comprise cyclical parthenogens (holocyclic, which are facultative asexuals with an annual sexual phase), obligate parthenogens (anholocyclic, which never recombine) and lineages for which only some of the autumnal offspring contribute to the sexual phase, that is, androcyclic forms that can produce a few males and intermediate forms that produce a few male and female sexuals (see Delmotte et al, 2001;Simon et al, 2002 for further details). Survival rates of the different types are related to the severity of the winter, since sexuals produce cold-hardy eggs, whereas lifecycle types without this facility overwinter as live individuals, which are more susceptible to low temperature mortality.…”
Section: Introductionmentioning
confidence: 99%
“…Rare automixis (spontaneous development of unfertilized eggs) occurs in many species [1,81]. If this becomes more common, forms of automixis maintaining heterozygosity in centromere regions might be selectively favoured and recombination suppressed, eventually leading to meiosis-derived asexuality with the same genetic consequences as mitosis [87][88][89][90][91]. Indeed, in Arabidopsis, meiosis can be transformed to genetically resemble mitosis, but modification of several genes is needed to achieve this [92][93][94].…”
Section: (C) Meiosis Modifications and Loss Of Sexmentioning
confidence: 99%