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<br />. <br /> <br />. <br /> <br />. <br /> <br />REFERENCE NUMBER: <br /> <br />CITATION: <br /> <br />026 <br /> <br />Bulb, D.G., R. W. Murphy, and L. Ulmer. 1987. Population <br />differentiation and introgressive hybridization of the tlannelmouth <br />sucker and of hatchery and native stocks of the razorback sucker. <br />Transactions of the American FISheries Society. 116(1):103-110. <br /> <br />SPECIES AND LIFE STAGE: <br /> <br />TOPICS: <br /> <br />KEYWORDS: <br /> <br />RZ. RZ_ADU, RZ_JUV <br /> <br />Research <br /> <br />RAZORBACK SUGKER. GENETICS, INTROGRESSIVE <br />HYBRIDIZATION, FLANNELMOUTH SUCKER, <br />ELECTROPHORESIS <br /> <br />SUMMARY: A problem regarding the management of any fish species that is artificially mass-produced <br />concerns the maintenance of the natural gene pooL Sampling error results in the enhancement <br />of the frequencies of some alleles and the reduction of others in the necessarily small <br />subsample of the wild population. This inherent characteristic of hatchery propagation coupled <br />with the razorback's tendency to hybridize naturally with other catostomids is cause for concern <br />when considering hatchery augmentation of natural populations. <br /> <br />Flannelmouth specimens for this study were obtained from the Virgin River in Arizona, the <br />mouth of the Paria River in AZ. the Little Colorado river drainage, AZ. Upper Colorado <br />River near Grand Junction, CO. Razorback specimens were obtained from Lake Mohave, AZ, <br />Senator Wash Reservoir, CA, and form Dexter national FISh Hatchery, NM. Brain, liver, <br />heart, and skeletal muscle tissues were used for electrophoresis. Gene prodUCts compared <br />included acid phosphatase, alcohol dehydrogenase, creatine kinase, glycerol-3-phosphate <br />dehydrogenase and several others. <br /> <br />Flannelmouth sucker were polymorphic in 9 of 21 loci in at least one of the geographic <br />locations. Within each of these locations, genotype arrays were within Hardy-Weinberg <br />expectations of genetic variability. Between the different geographic locations, statistically <br />sigJIifi~t structuring of gene flow patterns exisL Indicating geographic limitations of certain <br />polymorphism, though no complete allelic difference. Razorback sucker were polymorphic in <br />11 out of 21 loci in at least one of the geographic locations. Within each of these sample <br />populations genotype arra-ys were within Hardy-Weinberg expectations except for the Dexter <br />National FISh Hatchery population which shOWed excessive gene restriction in one loci. <br />Between the different geographic locations no structuring of gene flow patterns was noted. <br />Four loci were identified that were species-specific and could be used as marker loci. Two of <br />these four loci have allelic distributions suggesting some gene flow between the two species. <br />Both alleles are present in both species and the predominant allele in each species is present <br />in low frequency in the other species. Gene flow is proceeding both from tlannelmouth to <br />razorback sucker and from razorback to flannelmouth sucker. There is the possibility that both . <br />alleles at both loci were present in a. common ancestor of the catostomids. Evidence of <br />introgression in tlannelmouth sucker is found in the Virgin River sample and the upper <br />Colorado River sample. Introgression is apparently rare enough for the species to maintain <br />integrity of their respective gene pools in the wild. The current hatchery stock at Dexter has <br />not been appreciably affected by sampling error in favor of introgressed genes form <br />flanneJmouth suckers, and has fewer introgressed genes than parental stock from Lake Mohave. <br />As long as breeding stock continues to be obtained form natural populations, the breeding <br />program for razorback suckers at Dexter can be quite successful Programs that select <br />subsequent breeding stock from their own reared stock are ill advised for the razorback. <br /> <br />A-27 <br />