Seasonal Changes in Feeding of Coho and Chinook (Spring) Salmon in Southern British Columbia Waters

1962 ◽  
Vol 19 (5) ◽  
pp. 851-866 ◽  
Author(s):  
A. Prakash

Food study based on the stomach analyses of 551 chinook salmon (Oncorhynchus tshawytscha) and 659 coho salmon (O. kisutch) collected from the various localities along the southern British Columbia coast during the summer of 1957 revealed that herring followed by crustaceans formed the most important items of the diet of the two species. Coho salmon exhibited a more pelagic and varied diet than chinook salmon caught in the same area. Definite seasonal fluctuations in the composition of food and feeding intensity were noticed. Considerable amounts of Crustacea were taken in early summer months and after that fish assumed importance.Qualitative and quantitative differences in the feeding of these two species on the east and west coasts of Vancouver Island appear to warrant the establishment of two food type areas, Although herring constitute the major food item of both spring and coho salmon, evidences are presented in support of the hypothesis that a change in herring stock is not likely to affect salmon abundance in British Columbia coastal waters.

1986 ◽  
Vol 43 (3) ◽  
pp. 565-573 ◽  
Author(s):  
Eric B. Taylor ◽  
P. A. Larkin

In Slim Creek, a tributary to the upper Fraser River east of Prince George, B.C., chinook salmon (Oncorhynchus tshawytscha) fry summer and overwinter in their natal stream before migrating seaward as yearlings; they are "stream-type" in juvenile life history pattern. From the Harrison River, a tributary to the lower Fraser River, chinook fry migrate to the Fraser River estuary sometime during their first spring or early summer; they are "ocean-type." Newly emerged chinook fry from Slim Creek showed a stronger positive current response, were more aggressive in mirror image stimulation tests and intra- and inter-specific (with coho salmon (O. kisutch) fry) stream tank tests, and had larger and more brightly colored median fins than chinook fry from the Harrison River. These differences between Slim Creek and Harrison River chinook fry are in a direction consistent with their different patterns of length of freshwater residence as juveniles, since aggressive behavior, positive rheotaxis, and bright fin coloration are important components of extended stream residence in salmonids.


1983 ◽  
Vol 61 (9) ◽  
pp. 1991-1994 ◽  
Author(s):  
T. E. McDonald

An examination of 220 chinook salmon (Oncorhynchus tshawytscha), 84 coho salmon (O. kisutch), 145 steelhead trout (Salmo gairdneri), and 21 cutthroat trout (S. clarki) for Ceratomyxa shasta (Myxozoa: Myxosporea) from 16 localities in the Fraser River drainage, British Columbia, showed that at all sites examined these salmonid species were infected, with a prevalence ranging between 11 and 100%. The study concludes that C. shasta, the causative agent of the salmonid disease ceratomyxosis, is widely distributed in the Fraser drainage basin and discusses these results in relation to proposed fish culture in the region.


1999 ◽  
Vol 77 (7) ◽  
pp. 1161-1169 ◽  
Author(s):  
John R Candy ◽  
Thomas P Quinn

To characterize adult chinook salmon (Oncorhynchus tshawytscha) migratory behavior, we used ultrasonic tracking to describe their vertical and horizontal movements in upper Johnstone Strait, British Columbia during 1990-1992. Movement patterns varied: several fish showed a postrelease "escape" response and a protracted "recovery" period, with evidence of diel patterns of vertical and horizontal movements becoming apparent after 8 h. After release, 12 of the 32 chinook salmon that were tracked tended to dive deep. Chinook salmon that dived deep (>200 m) were significantly larger than fish that remained nearer the surface (mean fork length, 87.2 vs. 77.3 cm, respectively), and deep diving was not correlated with aspects of handling that might have stressed the fish. The mean depth of travel calculated over all tracks was 70 m and the maximum depths were between 300 and 400 m. Average depths of travel were shallower during the day (25-64 m) than at night (49-78 m). Overall, mean ascent and descent rates were similar (11-12 m/5 min). Gross travel rates (ground speed), defined as the distance moved during 5-min intervals, averaged 1.9 km/h, but tidal currents could have influenced these estimates. Net travel rates, defined as the distance between the point of release and track termination, were slower than gross rates, averaging 0.60 km/h. Average grounds speeds were more rapid during the day (1.9-3.2 km/h) than at night (1.7-2.5 km/h). Compared with sockeye salmon tracked in the same area during 1985-1986, chinook salmon moved more slowly, in both gross and net travel rates, and swam deeper.


1999 ◽  
Vol 56 (4) ◽  
pp. 578-589 ◽  
Author(s):  
Jeffrey J Hard ◽  
William R Heard

In 1976 chinook salmon (Oncorhynchus tshawytscha) gametes from the Chickamin and Unuk rivers in southeastern Alaska were transplanted 250 km to establish hatchery runs at Little Port Walter (LPW), Baranof Island. From 1977 to 1989, 1 862 058 marked smolts from 12 broods were released from LPW. Homing and straying were estimated from adult recoveries at 25 locations in Alaska and British Columbia between 1981 and 1989. Of 22 198 LPW fish recovered over this period, 21 934 (98.8%) were collected at LPW. Of 264 fish recovered elsewhere, 38.3% were within 7 km of LPW; 64.4% were within 25 km of LPW. No LPW fish were recovered from the ancestral rivers, but nine fish were recovered from rivers supporting wild chinook salmon. Straying declined with distance from the release site but varied between hatcheries and streams. Straying declined with increasing age and run size. Straying was similar between the populations but varied among broods, and analysis of straying in experimental groups provided evidence for a heritable component. Males strayed more often than females. Population, gender, run size, and recovery age interacted to produce substantial variation in straying, indicating that run composition can produce complex straying responses.


2020 ◽  
Vol 43 (7) ◽  
pp. 719-728 ◽  
Author(s):  
Maureen K. Purcell ◽  
Rachel L. Powers ◽  
Torunn Taksdal ◽  
Doug McKenney ◽  
Carla M. Conway ◽  
...  

1993 ◽  
Vol 50 (6) ◽  
pp. 1198-1207 ◽  
Author(s):  
Kurt D. Fausch

Replicate experiments were conducted in the Salmon River, British Columbia, during early summer 1990 to test the relative importance of velocity refuge, visual isolation, and overhead cover to microhabitat selection by steelhead (Oncorhynchus mykiss) parr and age-0 coho salmon (O. kisutch). Four types of artificial Plexiglas structures, the first three of identical construction, had different portions painted to provide increasing habitat complexity: velocity refuge alone, velocity refuge with visual isolation, all three features combined, and overhead cover alone. Steelhead parr selected structures with overhead cover alone or all three features significantly more often than those without overhead cover. Steelhead also selected structures adjacent to the swiftest velocities available and closest to other natural overhead cover, which accounted for most differences in use of the same structure in different locations. In contrast, few age-0 coho salmon used any structures. Those that did selected the three types of structures with velocity refuge about equally, but significantly more often than those with overhead cover alone, regardless of their location. Field experiments such as this hold promise for elucidating mechanisms of habitat selection by stream salmonids.


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


1997 ◽  
Vol 54 (7) ◽  
pp. 1585-1592 ◽  
Author(s):  
M J Bradford ◽  
G C Taylor

Immediately after emergence from spawning gravels, fry of stream-type chinook salmon (Oncorhynchus tshawytscha) populations from tributaries of the upper Fraser River, British Columbia, distribute themselves downstream from the spawning areas, throughout the natal stream, and into the Fraser River. We tested the hypothesis that this range in dispersal distances is caused by innate differences in nocturnal migratory tendency among individuals. Using an experimental stream channel, we found repeatable differences in downstream movement behaviour among newly emerged chinook fry. Fish that moved downstream were larger than those that held position in the channel. However, the incidence of downstream movement behaviours decreased over the first 2 weeks after emergence. We propose that the variation among individuals in downstream movement behaviour we observed leads to the dispersal of newly emerged fry throughout all available rearing habitats. Thus, between- and within-population variation in the freshwater life history observed in these populations may be caused by small differences in the behaviour of individuals.


1995 ◽  
Vol 52 (7) ◽  
pp. 1376-1384 ◽  
Author(s):  
Robert H. Devlin ◽  
Timothy Y. Yesaki ◽  
Edward M. Donaldson ◽  
Shao Jun Du ◽  
Choy-Leong Hew

Transgenic Pacific salmon have been produced by microinjection of a DNA construct consisting of chinook salmon (Oncorhynchus tshawytscha) growth hormone sequences driven by an ocean pout (Macrozoarces americanus) antifreeze protein promoter. This construct was retained in approximately 4% of fish derived from injected eggs, and resulted in dramatic enhancement of growth relative to controls. For coho salmon (O. kisutch) at 15 months of age, the average size of transgenic fish was more than 10-fold that of controls, with the largest fish more than 30-fold larger than nontransgenic siblings. Dramatic growth enhancement was also observed in transgenic rainbow trout (O. mykiss), cutthroat trout (O. clarki), and chinook salmon using this same gene construct. Transgenic coho salmon underwent precocious parr–smolt transformation during their first fall, approximately 6 months in advance of their nontransgenic siblings. At 2 years of age, five male transgenic coho salmon became sexually mature, and four of these transmitted the gene construct to sperm, the negative fish being transgenic in blood but not fin tissue. These results show that while some fish are mosaic for the gene construct in different tissues, most are transgenic in both germline and somatic tissue.


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