1995
DOI: 10.1086/285753
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Multilevel Selection in Natural Populations of Impatiens capensis

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Cited by 91 publications
(126 citation statements)
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References 48 publications
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“…Studies of multilevel selection in plant populations (e.g. [42,43]) suggest that kin groups should indeed be selected to reduce their competitiveness in this way. Still, the appeal of kin recognition is that some species (those that experience variation in local relatedness) may have the ability to acquire additional information about the relatedness of neighbours, and if so, cooperation could be identified by experiment.…”
Section: Discussionmentioning
confidence: 99%
“…Studies of multilevel selection in plant populations (e.g. [42,43]) suggest that kin groups should indeed be selected to reduce their competitiveness in this way. Still, the appeal of kin recognition is that some species (those that experience variation in local relatedness) may have the ability to acquire additional information about the relatedness of neighbours, and if so, cooperation could be identified by experiment.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies of partially selfing plant species have detected directional selection on a variety of quantitative traits (Kalisz 1986;Stewart and Schoen 1987;Brassard and Schoen 1990;Mitchell-Olds and Bergelson 1990b;Johnston 1991;Fenster and Ritland 1994;Stevens et al 1995) and it is possible that some of these results could have been biased by the mating system. For example, a study of the self-compatible annual Collinsia verna found that directional selection acted on the timing of germination (Kalisz 1986), a trait which has been shown to exhibit inbreeding depression (Ka- lisz 1989).…”
Section: Measurements Of Selection: Biases Due To Mating System and Imentioning
confidence: 99%
“…Studies designed to measure the magnitude and form of phenotypic selection frequently employ the regression techniques described by Lande and Arnold (1983), while studies designed to quantify the ability of a population to respond to selection often use the standard breeding designs of quantitative genetics to estimate additive genetic variances and covariances (Bulmer 1980;Falconer 1981;Mather and Jinks 1982). These methods, particularly those of quantitative genetics, were developed primarily in the context of randomly mating reference populations, and yet frequently studies using quantitative genetics and selection analyses are conducted on populations that are at least partially inbred (e.g., Lawrence 1965;Gale and Arthur 1972;Lawrence 1972;Kalisz 1986;Mitchell-aids 1986;Stewart and Schoen 1987;Brassard and Schoen 1990;Mitchell-Olds and Bergelson, 1990a,b;Johnston 1991;Carr and Fenster 1994;Fenster and Ritland 1994;Robertson et al 1994;Schoen et al 1994;Stevens et al 1995). Unfortunately, the interpretation of estimates of additive genetic variances/covariances or of the selection gradients obtained from experiments on partially inbred populations is complicated when there is inbreeding depression for the quantitative characters examined.…”
mentioning
confidence: 99%
“…This is not surprising, given that Lande's selection theory that originally sparked much of the interest in the constancy of G is individual selection theory (Lande 1979), and evolutionary biology has been dominated by Darwin's individual selection paradigm. The increasing evidence in the genetic school of multilevel selection theory (e.g., Wade 1977;Craig 1982;Goodnight 1985;Wade and Goodnight 1991;Stevens et al 1995;Muir 1996; see also Goodnight and Stevens, in press) requires that we gain more familiarity with population-level analyses and an understanding of how evolutionary processes such as inbreeding affect population-level traits and phenomena.…”
mentioning
confidence: 99%