1998
DOI: 10.1111/j.1469-1795.1998.tb00015.x
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Microsatellite analysis of genetic diversity in fragmented South African buffalo populations

Abstract: Genetic variation was measured in 105 African buffalo from four populations in South Africa to investigate the effects of habitat fragmentation. Levels of heterozygosity, allelic diversity and genetic differentiation among populations were quantified using seven polymorphic microsatellite markers. There was a significant correlation between the amount of genetic variation and population size, and differentiation was detected among all populations measured by F ST and R ST . We used likelihood analysis to infer… Show more

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Cited by 99 publications
(84 citation statements)
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“…In the immigration-drift-equilibrium model, the degree of differentiation is a measure of the relative strength of drift versus immigration (Rannala and Hartigan 1996), while in the non-equilibrium drift model it is related to the time since fragmentation (scaled by population size) (O'Ryan et al 1998). 2mod first estimates the probability of obtaining each dataset assuming that the mutation rate is much smaller than the immigration rate in the gene flow model, and that the reciprocal of the mutation rate is much longer than the divergence time in the drift model.…”
Section: Demographic Historymentioning
confidence: 99%
“…In the immigration-drift-equilibrium model, the degree of differentiation is a measure of the relative strength of drift versus immigration (Rannala and Hartigan 1996), while in the non-equilibrium drift model it is related to the time since fragmentation (scaled by population size) (O'Ryan et al 1998). 2mod first estimates the probability of obtaining each dataset assuming that the mutation rate is much smaller than the immigration rate in the gene flow model, and that the reciprocal of the mutation rate is much longer than the divergence time in the drift model.…”
Section: Demographic Historymentioning
confidence: 99%
“…The effective population size (N e ) of both wild and captive populations was estimated with the program DLIK (available at: http://www.rubic.rdg.ac.uk/~mab/software.html). This program uses coalescent theory and Monte Carlo sampling of gene frequencies to generate a probability distribution of the parameter T/N e , where T is the number of generations that have elapsed since the population was founded and N e is the effective population size over that period (O'Ryan et al 1998). A generation time of 8.34 for Cynopterus bats (Storz et al 2001b) was used as a best estimate for Pteropus bats and a maximum effective population size of 1,000 was assumed based on previous census data (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…For example, information on census size is often available, and if the rate of inbreeding for a given census size can be calibrated for one population then predictions may be made about other (comparable) populations on other (comparable) timescales (e.g. O'Ryan et al, 1998).…”
Section: Estimating Effective Population Sizementioning
confidence: 99%
“…An additional problem is that the evaluation of p(n c |T /(2N e ), n s ) can be numerically unstable. O'Ryan et al (1998) use importance sampling (Griffiths and Tavaré, 1994) as an alternative method of evaluation, and this is embedded within a Markov chain Monte Carlo (MCMC) sampler to infer marginal posterior densities for individual parameters (see Beaumont, 2003a, for a detailed description of this general approach). The general scheme for two populations is illustrated in Figure 30.1.…”
Section: Estimating N E From Two Derived Populationsmentioning
confidence: 99%
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