First-Year Growth Rate of Sixes River Chinook Salmon as Inferred from Otoliths: Effects on Mortality and Age at Maturity

Author(s):  
John D. Neilson ◽  
Glen H. Geen
1993 ◽  
Vol 130 (2) ◽  
pp. 314 ◽  
Author(s):  
Nat B. Frazer ◽  
Judith L. Greene ◽  
J. Whitfield Gibbons

Author(s):  
Brian R. Beckman ◽  
Donald A. Larsen ◽  
Beeda Lee-Pawlak ◽  
Walton W. Dickhoff
Keyword(s):  

1993 ◽  
Vol 23 (8) ◽  
pp. 1507-1513 ◽  
Author(s):  
John M. Randall ◽  
Marcel Rejmánek

The biennial thistle Cirsiumvulgare (Savi) Tenore significantly reduced ponderosa pine (Pinusponderosa Dougl. ex Laws.) seedling growth during the second year of infestation but had insignificant effects in the first year when all thistles were in the rosette stage. Pine stem diameter relative growth rate was significantly negatively correlated with four different indices of thistle interference and with visual estimates of thistle cover. Total thistle density (adults + rosettes) within 2.0 m of target seedlings best explained differences in stem relative growth rate, but density of adults alone and visual estimates of thistle cover were nearly as good. Simple regressions indicated that soil moisture and pine predawn leaf water potential were significantly negatively correlated with thistle density and significantly positively correlated with stem relative growth rate, but multiple regressions and path analyses indicated that their effects on seedling growth were negligible relative to the other (unexplained) effects of thistle density. Foliar nitrogen, phosphorus, and potassium concentrations were not significantly correlated with thistle density and failed to explain differences in seedling growth. Although it remains unclear how thistles suppressed pine seedling growth, if these results hold true at other sites, plantation managers will have at their disposal relatively easy methods for assessing thistle interference.


1993 ◽  
Vol 50 (2) ◽  
pp. 435-442 ◽  
Author(s):  
Daniel D. Heath ◽  
Nicholas J. Bernier ◽  
John W. Heath ◽  
George K. Iwama

Eight full- and half-sib families of chinook salmon (Oncorhynchus tshawytscha) were held during egg development at two temperatures (8.0 and 10.2 °C). As fry, these families were measured for relative growth rate, initial and final wet weight, hematocrit values before and 2 h after a 30-s handling stress, and plasma cortisol and glucose concentrations before and after stress. Significant sire effects were found for all measured traits, and significant dam effects were found for all traits except for the poststress increases in cortisol concentrations. There were significant genotype-by-environment interactions for all traits except unstressed (control) plasma glucose concentrations. Incubation temperature had a significant effect on relative growth rate and final wet weight only. We found a significant correlation between poststress plasma glucose concentration and relative growth rate for all fish, independent of family, while resting plasma cortisol concentration and poststress hematocrit correlated with wet weight only when analyzed within the eight individual families. Genetic contributions to stress-related parameters and genotype-by-environment interactions should be considered as a factor in stress-related research with fish.


1983 ◽  
Vol 34 (3) ◽  
pp. 461 ◽  
Author(s):  
SA Shepherd ◽  
WS Hearn

The growth of H. laevigata Donovan and H. ruber Leach was studied at several sites in South Australia by fitting the von Bertalanffy growth equation to growth data, supplemented by analysis of length- frequency distributions. Juvenile individuals of H. laevigata grow at an average rate of 0.9 mm per week, reaching a length of about 40 mm in 1 year at West Island; at Waterloo Bay H. laevigata can reach a length of 50 mm in the first year. After the first year, the annual growth coefficient (K) and the asymptotic length (L∞) for the two species at three sites are, respectively: H. laevigata-0.48 year-1 and 138 mm (West I.); 0.41 year-1 and 131 mm (Tipara Reef); 0.59 year-1 and 148 mm (Waterloo Bay); H, ruber-0 34 year-1 and 139 mm (West I.); 0.32 year-1 and 143 mm (Tipara Reef); 0 41 year-1 and 144 mm (Waterloo Bay). There are also seasonal differences in growth rate between species and between sites. These differences as well as differences in the annual growth rate within a species between sites are associated predominantly with differences in the food supply. There is differential growth between the sexes of H. laevigata at Waterloo Bay, where females grow 25% faster than males and reach a larger size.


1981 ◽  
Vol 38 (12) ◽  
pp. 1636-1656 ◽  
Author(s):  
W. E. Ricker

Of the five species of Pacific salmon in British Columbia, chinook salmon (Oncorhynchus tshawytscha) and coho salmon (O. kisutch) are harvested during their growing seasons, while pink salmon (O. gorbuscha), chum salmon (O. keta), and sockeye salmon (O. nerka) are taken only after practically all of their growth is completed. The size of the fish caught, of all species, has decreased, but to different degrees and over different time periods, and for the most part this results from a size decrease in the population. These decreases do not exhibit significant correlations with available ocean temperature or salinity series, except that for sockeye lower temperature is associated with larger size. Chinook salmon have decreased greatly in both size and age since the 1920s, most importantly because nonmaturing individuals are taken by the troll fishery; hence individuals that mature at older ages are harvested more intensively, which decreases the percentage of older ones available both directly and cumulatively because the spawners include an excess of younger fish. Other species have decreased in size principally since 1950, when the change to payment by the pound rather than by the piece made it profitable for the gill-netters to harvest more of the larger fish. Cohos and pinks exhibit the greatest decreases, these being almost entirely a cumulative genetic effect caused by commercial trolls and gill nets removing fish of larger than average size. However, cohos reared in the Strait of Georgia have not decreased in size, possibly because sport trolling has different selection characteristics or because of the increase in the hatchery-reared component of the catch. The mean size of chum and sockeye salmon caught has changed much less than that of the other species. Chums have the additional peculiarity that gill nets tend to take smaller individuals than seines do and that their mean age has increased, at least between 1957 and 1972. That overall mean size has nevertheless decreased somewhat may be related to the fact that younger-maturing individuals grow much faster than older-maturing ones; hence excess removal of the smaller younger fish tends to depress growth rate. Among sockeye the decrease in size has apparently been retarded by an increase in growth rate related to the gradual cooling of the ocean since 1940. However, selection has had two important effects: an increase in the percentage of age-3 "jacks" in some stocks, these being little harvested, and an increase in the difference in size between sockeye having three and four ocean growing seasons, respectively.Key words: Pacific salmon, age changes, size changes, fishery, environment, selection, heritability


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