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Last modified
7/14/2009 5:02:32 PM
Creation date
6/1/2009 12:00:57 PM
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UCREFRP
UCREFRP Catalog Number
7970
Author
Dowling, T. E. and W. L. Minckley.
Title
Genetic Diversity Of Razorback Sucker As Determined By Restriction Endonuclease Analysis Of Mitochondrial DNA.
USFW Year
1994.
USFW - Doc Type
Bureau of Reclamation, # 0-FC-40-09530-004,
Copyright Material
NO
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trays until hatching (96 to 168 hours post-fertilization}, then moved to holding tanks until <br />swim-up (approximately seven days post-hatch). Egg production per female ("fecundity") is <br />determined gravimetrically. Embryo viability (used as an estimator of expected hatch) is <br />assessed at 48 hours post-fertilization. Actual larval production is measured by water <br />displacement after hatching is complete. <br />Isolation and analysis of mtDNA.- Hatchery-produced razorback suckers were characterized <br />by restriction endonuclease analysis of mtDNA samples from three year classes (1987, 1989, <br />and 1990) using the enzymes described above. Composite haplotypes for each individual are <br />provided in Table 2 and Appendix I. <br />Statistical analysis.- Levels of genetic diversity within year classes were estimated as <br />described above. Significance of differences in h values among source and hatchery samples <br />was tested by randomly resampling the data (computer program modified by TED from <br />HAPLOID of Weir, 1990). A distribution of diversity values was generated by drawing 1000 <br />random samples of 10 individuals from the source population represented by our sample of 25 <br />individuals from Lake Mohave, and calculating diversity for each. Sampling of an individual <br />was followed immediately by its replacement; individuals could therefore be selected several <br />times or not at all in each replication. Mean diversity value for each set of 1000 resamples <br />and its 95% confidence interval were obtained from the distribution of diversity values (Weir, <br />1990). <br />Effect of broodstock size on h was also examined by computer simulation. The above <br />program was modified to sample a highly diverse source population (ranging from 2 to 100 <br />individuals, with each individual possessing a different haplotype) to generate 10,000 progeny. <br />Progeny haplotypes were obtained by randomly sampling parental haplotypes (with <br />replacement as described above). From this "hatchery stock," 1000 samples of 14 individuals <br />18 <br />
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