We analyzed intraspecific mitochondrial DNA variation in chinook salmon (Oncorhynchus tshawytscha) from drainages in the Yukon River (Alaska and Yukon Territory), the Kenai River (Alaska), and Oregon and California rivers; and chum salmon (O. keta) from the Yukon River and Vancouver Island, and Washington rivers. For each species, three different portions of the mtDNA molecule were amplified separately using the polymerase chain reaction and then digested with at least 19 restriction enzymes. Intraspecific sequence divergences between haplotypes were less than 0.01 base substitution per nucleotide. Nine chum salmon haplotypes were identified. Yukon River chum salmon stocks displayed more haplotypes (eight) than the stocks of Vancouver Island and Washington (two). The most common chum salmon haplotype occurred in all areas. Seven chinook salmon haplotypes were identified. Four haplotypes occurred in the Yukon and Kenai rivers and four occurred in Oregon/California, with only one haplotype shared between the regions. Sample sizes were too small to quantify the degree of stock separation among drainages, but the patterns of variation that we observed suggest utility of the technique in genetic stock identification.

Although the number of genetic markers available for fisheries research has steadily increased in recent years, there is limited information on their relative utility. In this study, we compared the preformance of different "classes" of genetic markers (mitochondrial DNA (mtDNA), nuclear DNA (nDNA), and allozymes) in terms of estimating levels and partitioning of genetic variation and of the relative accuracy and precision in estimating population allocations to mixed-stock fisheries. Individuals from eight populations of fall-run chum salmon (Oncorhynchus keta) from the Yukon River in Alaska and Canada were assayed at 25 loci. Significant differences in mitochondrial haplotype and nuclear allele frequencies were observed among five drainages. Populations from the U.S.-Canada border region were not clearly distinguishable based on multilocus allele frequencies. Although estimates of total genetic diversities were higher for the DNA loci (Ht = 0.592 and h = 0.647 for nDNA and mtDNA, respectively) compared with protein allozymes (Ht = 0.250), estimates of the extent of population differentiation were highly concordant across marker classes (mean theta = 0.010, 0.011, and 0.016 for allozymes, nDNA, and mtDNA, respectively). Simulations of mixed-stock fisheries composed of varying contributions of U.S. and Canadian populations revealed a consistent bias for overallocation of Canadian stocks when expected Canadian contributions varied from 0 to 40%, due primarily to misallocations among genetically similar border populations. No single marker class is superior for differentiating populations of this species at the spatial scale examined.

Substantial genetic divergence was found among chum salmon (Oncorhynchus keta) populations collected from North America and Russia. Five major groups of populations can be identified by geographic region: (1) lower Yukon River summer run; (2) upper Yukon River fall run; (3) Bristol Bay area; (4) Alaska Peninsula; and (5) Russia. Mean heterozygosities were 0.064, 0.062, 0.065, 0.064, and 0.063, respectively; and the percent polymorphic loci values at the 0.99 level were 33.7, 31.3, 32.6, 30.6, and 30.9%, respectively. The hierarchical gene diversity analysis showed that 95.42% of the diversity can be explained by heterogeneity within sites, 1.36% among sites, 0.49% between Yukon River run timing, 1.69% among areas, and 1.04% among countries. The Alaska Peninsula populations are genetically more similar to populations from Russia than to those from western Alaska, and two populations from the upper Yukon River are distinct from other nearby populations. Possible reasons for these findings concern the complex glacial histories of the watersheds.

Colonization of Frazer Lake (Kodiak Island, Alaska) by sockeye salmon (Oncorhynchus nerka) represents a rare, successful introduction of this species into a new environment. Eggs, fry, and adults were introduced repeatedly into Frazer Lake from 1951 to 1971. Donors originated from three source populations, each with different life histories: late-run lake shoreline spawners (Karluk Lake), early-run inlet tributary spawners (Red Lake), and late-run lake outlet spawners (Ruth Lake). We used six nuclear DNA (nDNA) microsatellite loci and mitochondrial DNA (mtDNA) to determine which donor population(s) had colonized the principal spawning habitats of Frazer Lake: three shoreline areas and four inlet tributaries. Based on nDNA comparisons, two shoreline-spawning populations were most similar to the shoreline donor, and the four tributary-spawning populations were most similar to the tributary donor. However, five of the seven Frazer Lake populations appeared to be influenced genetically by more than one donor. Genetic distances based on mtDNA were independent of life histories with high (relative to nDNA) interpopulation variation, suggesting significant female founder effects and poststocking drift. Our data suggest that life history adaptations of donor populations were critically important for successful colonization of Frazer Lake, thus underscoring the need to consider life history traits in other introduction and recovery programs.

The Tustumena Lake drainage in southcentral Alaska is glacially turbid and geologically young (<2,000 years old). Previous field studies identified at least three subpopulations of sockeye salmon Oncorhynchus nerka at Tustumena Lake, based on the distribution and timing of spawners. The subpopulations included early-run salmon that spawned in six clearwater tributaries of the lake (mid August), lake shoreline spawners (late August), and late-run fish that spawned in the lake's outlet, the Kasilof River (late September). Our objective was to determine the degree of genetic differentiation among these subpopulations based on restriction enzyme analyses of the cytochrome h gene of mitochondria! DNA and analyses of four polymorphic allozyme loci. Mitochondrial DNA haplotype frequencies for outlet-spawning sockeye salmon differed significantly from those of all other subpopulations. The most common (36%) haplotype in the outlet subpopulation did not occur elsewhere, thus suggesting little or no gene flow between outlet spawners and other spatially close subpopulations at Tustumena Lake. Allele frequencies at two allozyme loci also indicated a degree of differentiation of the outlet subpopulation from the shoreline and tributary subpopulations. Allele frequencies for three tributary subpopulations were temporally stable over approximately 20 years (based on a comparison to previously published results) despite initiation of a hatchery program in two of the tributaries during the intervening period. Collectively, our results are consistent with the hypothesis that significant genetic differentiation has occurred within the Tustumena Lake drainage since deglaciation approximately 2.000 years ago.