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4 <br />DRAFT <br />same chromosome. If this were the case in a series of closely related populations, one would <br />expect the same loci to be associated in each population. Alternatively, linkage disequi- <br />librium could be caused by selection on particular combinations of alleles at different loci. <br />Disequilibrium could also be caused by colonization of new habitat. If relatively few individ- <br />uals colonize a new site, the arrangement of alleles that they bring with them may persist <br />for a short time. Continuous dispersal into a population from a differentiated source could <br />also cause disequilibrium if historic residents of a site are compared to recent immigrants <br />In the captive population, loci 300 and 267 appear to be statistically associated (table 2). <br />Because it is not repeated across populations and the evidence for disequilibrium is weak, <br />it is likely this pattern results from the sampling effort associated with founding the Willow <br />Beach population. <br />3.6 Genetic variability <br />Neis.Diversity Sample.Size <br />Boulders 0.53 4.00 <br />Coyote Camp 0.63 15.00 ?$ <br />Salt Camp 0.65 17.007 <br />Willow Beach 0.68 63.00 <br />Table 3: Estimates of average Nei's Gene Diversity across loci for three wild-sampled pop- <br />ulations and one captive population (Willow Beach). Sample sizes refer to the number of <br />individuals sampled for at least one of six loci used to calculate averages <br />Table 3 provides estimates of Nei's gene diversity, 1- Ep' (Nei; 1973), for each population <br />considered in this study. The average diversities indicate little overall differences among wild <br />and captive populations. Furthermore, there is little evidence for differences in diversity <br />among wild-sampled populations. Diversity estimates are sample-size dependent. As a <br />result/, the marginally lower values for the Boulders site can be explained by the relatively <br />few fish sampled. Likewise, the slightly higher value for the captive population is also likely <br />to be due to the significantly larger sample size for this group. <br />3.7 Genotypic differentiation <br />Table 4 presents contingency table-based tests of differences in genotypic frequencies among <br />populations. Because so many genotypes are present in low frequencies in microsatellite data <br />in general and this dataset in particular, the significance of these comparisons was assessed <br />by simulating the null-distribution using Monte Carlo simulation methods (Rousset and <br />Raymond; 1997). Basically, this approach simulates the expected distribution of genotypes <br />among populations assuming no difference among the population pairs. The actual data are <br />then compared to this null-distribution and if they appear more extreme than the simulated <br />6