Abstract.-Life history traits in hatchery and wild spring Chinook salmon Oncorhynchus tshawytscha from the upper Yakima River were compared to determine whether locally adapted traits had diverged after one generation of state-of-the-art artificial propagation. Sex composition in wild-and hatchery-origin fish differed in three of four brood years (P 0.01). The proportion of hatchery males, primarily age 3, increased from 38% to 49% over time. Conversely, the sex composition of wild fish did not exhibit a similar linear trend. Most hatchery-and wild-origin fish reached maturity at age 4 (!76%), followed in magnitude by ages 3 and 5. Wild mean age at maturation demonstrated no significant trend over time, while hatchery mean age at maturation declined (P ¼ 0.05). Mean lengths of 3-5-year-old hatchery fish were shorter than those of wild fish of the same age (differences of 2.7 cm for age 3, 1.7 cm for age 4, and 1.9 cm for age 5). Likewise, body weights of hatchery fish were lower than those of wild fish (differences of 0.3 kg for age 3, 0.3 kg for age 4, and 0.6 kg for age 5), representing a change in body size of between 0.5 and 1.0 standard deviation (SD). Median arrival timing of hatchery and wild fish at a broodstock collection site just downstream of ancestral spawning grounds showed no consistent difference. However, the median arrival date of age-3 fish was 19-20 d later than that for fish of ages 4 and 5 (P , 0.01). Mean spawn timing of hatchery fish was significantly earlier (5.1 d) than that of wild fish in a ''common-garden'' experiment (P , 0.05). We estimate that fitness could be reduced by as much as 1-5% for traits diverging from their optima by 0.5-1.0 SD. The degree of genetic determination of the divergence is unknown, but future monitoring will help clarify this. Perhaps the most important conclusion of our study is that even a hatchery program designed to minimize differences between hatchery and wild fish did not produce fish that were identical to wild fish.

No abstract

We describe a conditional maximum likelihood procedure for estimating stock composition in a mixed-stock fishery, provided that samples can be collected from the contributing stocks in isolation from each other and that characters exist that differ significantly between stocks. The procedure presented can use discrete (electrophoretic, meristic) or continuous (morphometric) data or any combination of these data. The procedure is tested by simulations and is used to estimate stock compositions of chum salmon (Oncorhynchus keta) sampled in a test fishery near Vancouver Island, B.C., in 1981. The estimated composition in the test fishery agreed closely with the results of previous tagging studies in the same area.

First-generation hatchery and wild spring Chinook salmon Oncorhynchus tshawytscha from the upper Yakima River, Washington, were placed into an artificial stream and allowed to spawn. Seven independent test groups were placed into the stream from 2001 through 2005. No differences were detected in the egg deposition rates of wild and hatchery females. Pedigree assignments based on microsatellite DNA, however, showed that the eggs deposited by wild females survived to the fry stage at a 5.6% higher rate than those spawned by hatchery females. Subtle differences between hatchery and wild females in redd abandonment, egg burial, and redd location choice may have been responsible for the difference observed. Body size did not affect the ability of females to spawn or the survival of their deposited eggs. How long a female lived was positively related to her breeding success, but female origin did not affect longevity. The density of females spawning in portions of the stream affected both egg deposition and egg-to-fry survival. No difference, however, was found in the overall distribution patterns of the two types of females. Other studies that have examined the effects of a single generation of hatchery culture on upper Yakima River Chinook salmon have disclosed similar low-level effects on adult and juvenile traits. The cumulative effect of such differences will need to be considered when hatcheries are used to restore depressed populations of Chinook

Two populations of Paiute cutthroat trout (Salmo clarki seleniris) were compared meristically and electrophoretically with Lahontan cutthroat (S. c. henshawi) and rainbow trout (S. gairdneri) to elucidate population structure and verify the occurrence of introgressive hybridization. In Silver King Creek, both meristic and electrophoretic evidence indicated two populations were present, one appearing to be pure Paiute cutthroat, the other Paiute cutthroat introgressed with rainbow trout. Lahontan cutthroat introgression was a possibility in Silver King Creek but could not be evaluated because of the strong meristic and electrophoretic similarity of Paiute and Lahontan cutthroat. The other Paiute population, Cottonwood Creek, meristically appeared to be pure Paiute cutthroat but electrophoretic data indicated it was introgressed with rainbow trout. The existence of the two Silver King Creek populations indicated introgression was incomplete in that stream; introgression appeared to be complete in Cottonwood Creek. The meristic similarity of Cottonwood Creek trout to pure Paiute cutthroat was probably a result of strong selection by management agencies for a Paiute cutthroat phenotype. Electrophoresis was more discriminating than meristic analysis in this study in detecting introgression. Electrophoresis also allowed more detailed analysis of population structure than meristics because of the difference in complexity of the genetic systems analyzed by the two techniques. However, the application of both techniques contributed greatly to our understanding of introgression in the Paiute cutthroat and demonstrated the complementarity of the two approaches.Key words: Salmo clarki, Salmo gairdneri, Paiute cutthroat, Lahontan cutthroat, meristics, electrophoresis, introgression, hybridization, gametic disequilibrium, principal components