1989
DOI: 10.1038/hdy.1989.90
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Spatial autocorrelation of genotypes in populations of Impatiens pallida and Impatiens capensis

Abstract: The genetic control and small scale spatial distributions of three conspicuous genetic polymorphisms-presence or absence of corolla spotting, yellow or white corolla colour, and presence or absence of stem waxiness-were studied in populations of the plant species Impati ens pallida and I. capensis occurring in Québec, Canada. The corolla spotting and colour morphs in I. pallida each appear to be determined by different pairs of unlinked loci. Dominant alleles at each locus pair are required for the expression … Show more

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Cited by 76 publications
(44 citation statements)
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“…Consistently, most studies involving large populations have elicited patterns of spatial genetic organization over short distances (Epperson & Clegg, 1986;Schoen & Latta, 1989;Perry & Knowles, 1991;Schnabel et at., 1991;Wagner et a!., 1991;Shapcott, 1995), although some exceptions seem to occur (Levin, 1976;Dewey & Heywood, 1988). The existence of spatial structuring in large populations facilitates the generation and maintenance of high levels of variability with which to sustain efficient reproductive performance, survive stochastic events or adjust to novel fluctuating environments (Huenneke, 1991).…”
Section: Introductionmentioning
confidence: 83%
“…Consistently, most studies involving large populations have elicited patterns of spatial genetic organization over short distances (Epperson & Clegg, 1986;Schoen & Latta, 1989;Perry & Knowles, 1991;Schnabel et at., 1991;Wagner et a!., 1991;Shapcott, 1995), although some exceptions seem to occur (Levin, 1976;Dewey & Heywood, 1988). The existence of spatial structuring in large populations facilitates the generation and maintenance of high levels of variability with which to sustain efficient reproductive performance, survive stochastic events or adjust to novel fluctuating environments (Huenneke, 1991).…”
Section: Introductionmentioning
confidence: 83%
“…Os genótipos individuais podem ser tratados como classes nominais, com suas distribuições espaciais descritas em termos de estatísticas de contagem de vizinhos pareados "join-counts" (Epperson & Clegg 1986, Epperson & Allard 1989, Schoen & Latta 1989, Epperson 1995. De forma alternativa, os indivíduos podem ser caracterizados por suas freqüências alélicas, com a distribuição espacial dos alelos sendo descrita em termos de um coeficiente de autocorrelação, usualmente o coeficiente I de Moran (Dewey & Heywood 1988, Campbell & Dooley 1992.…”
Section: Introductionunclassified
“…Contudo, os estudos dos padrões espaciais de variabilidade genética dentro de populações têm mostrado o poder da análise de autocorrelação espacial para descrever a estrutura genética e para detectar seleção natural (Sokal & Oden 1978b, Epperson & Clegg 1986, Dewey & Heywood 1988, Epperson & Allard 1989, Schoen & Latta 1989, Knowles et al 1992, Shea & Furnier 2002.…”
Section: Introductionunclassified
“…Email: rngm50cornell.edu terns of genotypes have been interpreted in plant populations (Epperson 1990;Heywood 1991). In the absence of discernible environmental heterogeneity, nonrandom clustering of genotypes has been interpreted as evidence for local pollen and seed dispersal (Epperson & Clegg 1986;Schoen & Latta 1989;Campbell & Dooley 1991;Schnabel et al 1991;Maki & Masuda 1993). Conversely, the absence of spatial genetic structure has been taken for evidence that gene flow is not restricted on a local scale (Waser 1987;Dewey & Heywood 1988; Epperson &r Allard 1989).…”
Section: Introductionmentioning
confidence: 99%