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A <br />DRAFT <br />4 Results and Conclusions <br />Theoretical results indicate that in those populations (with the exception of Boulders) that <br />were sampled, it is likely that the majority of genetic variation was obtained. As a result, <br />it seems reasonable to compare these wild-sampled populations to the captive population to <br />construct a test of whether the captive population represents wild stock. <br />Initial examination of the raw microsatellite data indicated that they are well suited to <br />estimate neutral genetic variation in the captive and wild populations. This examination was <br />followed by binning of alleles to facilitate the rest of the analyses presented in this report. <br />Examination of Hardy-Weinberg equilibrium revealed that the loci devised for bonytail <br />do not result in null alleles in Humpback chub. Linkage disequilibrium analyses also indicate <br />that loci can be treated as genetically independent markers. <br />To address the question of whether the captive population represents the wild sampled <br />fish, I ran a genotypic and allelic comparison. The genotype frequencies did differ among <br />populations, but it is unclear whether this difference would persist if subsequent generations <br />from each population were analyzed. In other words, this difference may be due to the <br />particulars of segregation in the generations sampled. The pairwise allelic analysis indicates <br />that there is very little difference between the wild-sampled and captive population. The one <br />exception is Boulders, and this population is not well sampled. My overall interpretation of <br />these data is that the genetic markers in the captive population adequately, but not perfectly, <br />represent the genetic variation present in wild populations of Humpback chub. As a result, <br />I believe that the Willow Beach broodstock is an important source of genetic material, and <br />maintaining this broodstock should be a management priority. <br />4.1 Recommendations for future work <br />To develop a stronger case for the conclusions above, I would recommend several things. <br />First, it is important to sample all wild populations sufficiently to provide a comparison to <br />the captive population. In particular, Boulders could be better represented in this dataset. <br />Further field sampling efforts should also target Salt Camp and Coyote Camp populations, <br />if possible, to capture changes that may have occurred among demographic cohorts. Second, <br />additional loci would provide better information on which to base inference. Eleven loci <br />were developed for bonytail and have been shown to amplify IN- umpback chub genomic DNA <br />(Keeler-Foster et al.; 2004). Therefore, it may not be too difficult to add to the loci already <br />characterized in this study. Finally, for the remaining loci, especially those shown to have <br />large amounts of missing data such as locus 226, it would be advisable to increase the number <br />of individuals with resolved alleles. <br />Finally, I believe that it is important to consider quantitative variation in the captive <br />and wild populations. If possible, it would be advisable to develop and analyze a dataset <br />that included both the marker genetics and phenotypes of both wild and captive fish. Such <br />phenotypes could include standard lengths, mass, fin ray counts, and other relatively easy <br />to assess morphological characteristics. <br />8