Density‐dependent effects of eastern Kamchatka pink salmon ( Oncorhynchus gorbuscha ) and Japanese chum salmon ( O. keta ) on age‐specific growth of western Alaska chum salmon

2020 ◽  
Vol 30 (1) ◽  
pp. 99-109
Author(s):  
Tessa J. Frost ◽  
Ellen M. Yasumiishi ◽  
Beverly A. Agler ◽  
Milo D. Adkison ◽  
Megan V. McPhee
1965 ◽  
Vol 22 (6) ◽  
pp. 1477-1489 ◽  
Author(s):  
H. T. Bilton ◽  
W. E. Ricker

Among 159 central British Columbia pink salmon that had been marked by removal of two fins as fry and had been recovered in commercial fisheries after one winter in the sea, the scales of about one-third showed a supplementary or "false" check near the centre of the scale, in addition to the single clear-cut annulus. This evidence from fish of known age confirms the prevailing opinion that such extra checks do not represent annuli, hence that the fish bearing them are in their second year of life rather than their third. Unmarked pink salmon from the same area, and some from southern British Columbia, had a generally similar incidence of supplementary checks. In both marked and unmarked fish the supplementary checks varied in distinctness from faint to quite clear. In a sample of scales of 14 double-fin marked chum salmon which were known to be in their 4th year, all fish had the expected 3 annuli, and 12 fish had a supplementary check inside the first annulus.


2009 ◽  
Vol 87 (3) ◽  
pp. 221-228 ◽  
Author(s):  
A. Grant ◽  
M. Gardner ◽  
L. Nendick ◽  
M. Sackville ◽  
A. P. Farrell ◽  
...  

Juvenile pink salmon ( Oncorhynchus gorbuscha (Walbaum, 1792)) enter seawater (SW) shortly following emergence. Little is known about growth and development during this life-history stage when sensitivity to sea louse exposure may be high, an issue that is of current concern in British Columbia. We tested the hypothesis that growth and ionoregulatory development were similar in hatchery-raised (Quinsam) and wild (Glendale and One’s Point) juvenile pink salmon (measured over 22 weeks) following SW entry. Fish body mass increased from 0.20 ± 0.01 to 6.47 ± 0.37 g, with mean specific growth rates of 2.74% to 3.05% body mass·day–1 among the three groups. In all three groups, gill Na+–K+-ATPase (NKA) activity peaked at 12 µmol ADP·mg protein–1·h–1 following 8 weeks post-transfer to SW. Whole body Na+ and Cl– concentrations, which again did not differ among groups, were highest upon initial exposure to SW (~70 mmol·kg wet mass–1) and declined over time as gill NKA activity increased, indicating that the hypo-osmoregulatory capacity was not fully developed following emergence and initial entry into SW. Thus, consistent with our hypothesis, few differences were observed between hatchery-raised and wild juvenile pink salmon reared under laboratory conditions. These baseline data may be important for future studies in determining the effects of sea lice on wild juvenile pink salmon.


1971 ◽  
Vol 28 (5) ◽  
pp. 647-654 ◽  
Author(s):  
C. E. Walker ◽  
D. B. Lister

Transfers of pink salmon (Oncorhynchus gorbuscha) eggs were made to the Qualicum River in two years, utilizing 5.79 million eggs from Cheakamus River stock in 1963 and 6.85 million eggs from Bear River stock in 1964. Adult returns to the Qualicum River were 100 spawners in 1965, 1967, and 1969; 11,940 in 1966; 3000 in 1968; and 300 in 1970. Differences between the odd- and even-year plants were noted in times of egg-take (equivalent to time of spawning of donor stock), incubation, and fry emigration, lengths of emigrating fry, possibility of losses through predation by herring on estuarine fry, and direction of orientation to the recipient (Qualicum River) stream. Pronounced differences between donor stock in rate of return are thought to be primarily related to differences in spawning times and stream temperature. The decrease in numbers of adults in the even-year generation may have been due to lower freshwater survival during incubation as a result of suspected superimposition of chum salmon on the earlier deposited pink salmon eggs; the loss was estimated to be in the order of 46%.


1985 ◽  
Vol 42 (4) ◽  
pp. 659-668 ◽  
Author(s):  
N. Brent Hargreaves ◽  
Robin J. Lebrasseur

Predation on juvenile pink salmon (Oncorhynchus gorbuscha) and chum salmon (O. keta) by yearling coho (O. kisutch) was studied in marine enclosures in Masset Inlet, B.C. These experiments demonstrate that coho prey selectively upon pink salmon even when chums are both significantly smaller and more abundant than pink salmon. Reexamination of the results of similar experiments conducted in Burke Channel, B.C., also confirms that mortality was biased towards pink salmon. Prey species may be more important than prey size for coho that prey upon mixed populations of pink and chum salmon during early sea-life.


2014 ◽  
Vol 71 (4) ◽  
pp. 521-532 ◽  
Author(s):  
Noel R. Swain ◽  
Morgan D. Hocking ◽  
Jennifer N. Harding ◽  
John D. Reynolds

Pacific salmon (Oncorhynchus spp.) can subsidize freshwater food webs with marine-derived nutrients from their eggs, juveniles, and carcasses. However, trophic interactions between spawning salmon and freshwater fish across natural gradients in salmon subsidies remain unclear. We tested how salmon affected the diets and condition of two dominant freshwater consumers — prickly and coastrange sculpins (Cottus asper and Cottus aleuticus, respectively) — across a wide gradient of pink salmon (Oncorhynchus gorbuscha) and chum salmon (Oncorhynchus keta) biomass from 33 streams in the Great Bear Rainforest of British Columbia, Canada. Sculpin diets shifted from invertebrates and juvenile salmonids to salmon eggs when salmon arrived in autumn, with salmon-derived nutrient contributions to diets and sculpin condition increasing with increasing biomass of spawning salmon among streams. Season, habitat, and individual sculpin body size and species also mediated the effects of salmon on sculpin diet as inferred from their carbon and nitrogen stable isotope signatures. This study shows the timing and pathways by which spawning salmon influence the diets and condition of freshwater consumers, and some of the individual and environmental factors that can regulate uptake of salmon nutrients in streams, thus informing ecosystem-based management.


1987 ◽  
Vol 65 (7) ◽  
pp. 1823-1826 ◽  
Author(s):  
T. D. Beacham ◽  
R. E. Withler

We compared developmental stability as measured by fluctuating asymmetry within individual adults for gill raker and branchiostegal ray number and pectoral and pelvic fin length for three populations of chum salmon (Oncorhynchus keta) and one of pink salmon (Oncorhynchus gorbuscha). There was no association between individual heterozygosity calculated at 10 electrophoretic loci for chum salmon and 13 loci for pink salmon and magnitude of fluctuating asymmetry for the four morphological characters examined. More heterozygous individuals were not less asymmetrical, and thus our results provide no evidence to suggest that increased heterozygosity results in an increased canalization of morphology during development and growth.


2017 ◽  
Vol 74 (7) ◽  
pp. 1077-1087 ◽  
Author(s):  
Allan J. Debertin ◽  
James R. Irvine ◽  
Carrie A. Holt ◽  
Gladys Oka ◽  
Marc Trudel

Thirty-nine years of scale growth measurements from Big Qualicum River chum salmon (Oncorhynchus keta) in southern British Columbia demonstrated that competition and climate variation affect marine growth and age-at-maturity. A longitudinal study design that accounted for correlation among individuals revealed growth at all ages was reduced when the biomass of North American chum, sockeye (Oncorhynchus nerka), and pink salmon (Oncorhynchus gorbuscha) was high. When North Pacific Gyre Oscillation (NPGO) was positive, indicating increased primary productivity, predicted growth increased. Climate variation influenced competition effects. For instance, density-dependent competition effects increased when NPGO became more positive and Pacific Decadal Oscillation became more negative (indicating cool conditions), causing the greatest range in predicted scale size. Chum salmon are likely to exhibit continued reduction in growth at age due to increased ocean temperatures driven by climate change and high aggregate salmon biomass that includes hatchery releases. If evidence of biomass and climate effects presented here are common among Pacific salmon populations, reduction of hatchery releases should be considered.


1985 ◽  
Vol 42 (2) ◽  
pp. 312-319 ◽  
Author(s):  
Terry D. Beacham ◽  
Clyde B. Murray

The magnitude of within-stock variability of postorbital–hypural length and body depth was investigated for spawning pink salmon (Oncorhynchus gorbuscha) and chum salmon (O. keta) stocks. Variability of postorbital–hypural length and body depth of male pink salmon, all maturing at 2 yr of age, was greater than that for male chum salmon, maturing at ages of 3–5 yr. Female pink salmon were less variable for the two characters than all ages of female chum salmon, equally variable when only age 3 or age 4 female chum salmon were considered, and more variable in comparison with age 5 female chum salmon. Males were more variable for each character than females for both species. Small males of both species tend to resemble females when body depths are compared. It is suggested that small males mimic females to reduce aggression from larger males and gain access to spawning females.


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