Possible Effects of the Sitka Eddy on Sockeye (Oncorhynchus nerka) and Pink Salmon (Oncorhynchus gorbuscha) Migration off Southeast Alaska

1986 ◽  
Vol 43 (2) ◽  
pp. 498-504 ◽  
Author(s):  
Kevin Hamilton ◽  
Lawrence A. Mysak

The interannual variability of sockeye (Oncorhynchus nerka) and pink salmon (Oncorhynchus gorbuscha) catches during 1952–62 from southeast Alaska and northern British Columbia is examined in relation to the appearance and disappearance of the Sitka eddy in the offshore oceanic circulation. In years when this large (~300 km in diameter) and intense (surface currents ~0.5 m/s) vortex is present, the spawning migration routes of salmon returning to the Nass and Skeena rivers tend to be deflected southward. An analysis of salmon tagging data collected during 1957 (when the eddy was absent) and 1958 (when the eddy was present) supports this conclusion. The southward deflection during 1958 is a particularly interesting result in light of many other observations which show that several fish species were displaced northward during the 1958 warming of the northeast Pacific Ocean.

2006 ◽  
Vol 84 (1) ◽  
pp. 88-97 ◽  
Author(s):  
Meaghan J MacNutt ◽  
Scott G Hinch ◽  
Chris G Lee ◽  
James R Phibbs ◽  
Andrew G Lotto ◽  
...  

We assessed the prolonged swimming performance (Ucrit), metabolic rate (M-dotO2-min and M-dotO2-max), and oxygen cost of transport (COT) for upper Fraser River pink salmon (Oncorhynchus gorbuscha (Walbaum, 1792); 53.5 ± 0.7 cm FL) and sockeye salmon (Oncorhynchus nerka (Walbaum, 1792); 59.3 ± 0.8 cm FL) across a range of naturally occurring river temperatures using large Brett-type swim tunnel respirometers. Pink salmon were capable of similar relative critical swimming speeds (Ucrit) as sockeye salmon (2.25 FL·s–1), but sockeye salmon swam to a higher absolute Ucrit (125.9 cm·s–1) than pink salmon (116.4 cm·s–1) because of their larger size. Nevertheless, three individual pink salmon (Ucrit-max = 173.6 cm·s–1) swam faster than any sockeye salmon (Ucrit-max = 157.0 cm·s–1), indicating that pink salmon are far better swimmers than has been previously assumed. Metabolic rate increased exponentially with swimming speed in both species and was highest for pink salmon, but swimming efficiency (i.e., COT) did not differ between species at their optimal swimming speeds. The upper and lower limits of metabolism did not differ between species and both M-dotO2-min and M-dotO2-max increased exponentially with temperature, but aerobic costs of transport were independent of temperature in both species. Strong thermal dependence of both swimming performance and COT were expected but not demonstrated in either species. Overall, a higher degree of inter-individual variability in pink salmon swim performance and capacity suggests that this species might not be as locally adapted to particular river migration conditions as are sockeye salmon.


1994 ◽  
Vol 51 (S1) ◽  
pp. 9-15 ◽  
Author(s):  
William W. Smoker ◽  
Anthony J. Gharrett ◽  
Michael S. Stekoll ◽  
John E. Joyce

Variation of size, particularly among males, has a significant genetic basis in pink salmon (Oncorhynchus gorbuscha) in Auke Creek, southeast Alaska. Heritability (h2), based on variance components of 118 full sib − 59 paternal half sib families of mature fish tagged as fry with coded micro wires, are higher in males (h2 length: 0.8 ± 0.3 (mean ± SE); h2 weight: 0.6 ± 0.2, based on sire effect) than in females (h2 length: 0.3 ± 0.2; h2 weight: 0.4 ± 0.2). Realized heritability probably would be smaller because of environment variability between brood years in factors affecting size and growth. Estimates based on regression of offspring means on fathers' values are smaller (h2 length: 0.4 ± 0.1 in males; 0.2 ± 0.1 in females; h2 weight: 0.0 in males and 0.1 ± 0.1 in females). Estimates of genetic, environmental, and phenotypic correlations of length and weight are all >0.7 (SEs <0.1). Estimates of genetic correlation between length and day of migration from the sea are near 0.4 ± 0.2; estimates of environmental and phenotypic correlations between these traits are smaller (<0.2, SEs <0.1).


2012 ◽  
Vol 69 (9) ◽  
pp. 1499-1512 ◽  
Author(s):  
Skip McKinnell ◽  
Maxine Reichardt

Mortality of salmon in the ocean is considered to be greatest during the first few months and that its magnitude is an inverse of growth. First year marine growth (M1) in two Fraser River sockeye salmon ( Oncorhynchus nerka ) populations was positively correlated, reflecting a shared oceanic experience as postsmolts. M1 declined abruptly in both populations after 1977, corresponding to a well-documented change in climate. The reduction in average M1 was not accompanied by a detectable reduction in average survival. In both populations, M1 was significantly greater in even years when juvenile pink salmon ( Oncorhynchus gorbuscha ) are abundant in the Strait of Georgia, suggesting that interspecific competition there has little effect on M1. All correlations of M1 with regional pink salmon or sockeye salmon abundances, lagged to align ocean entry years, were negative, but few (pink) or none (sockeye) were statistically significant. The negative correlations were due to the long-term changes (pink salmon abundance increasing, sockeye M1 smaller). Odd year dominance of juvenile pink salmon in northern British Columbia, Canada, is persistent and corresponds with the biennial pattern of M1 variation in Fraser River sockeye salmon and may be the source of the significant odd–even year line effect on M1.


2001 ◽  
Vol 58 (8) ◽  
pp. 1648-1662 ◽  
Author(s):  
Zhenming Su ◽  
Milo D Adkison ◽  
Benjamin W Van Alen

In this paper, we present an improved methodology for estimating salmon escapements from stream count data. The new method uses a hierarchical Bayesian model that improves estimates in years when data are sparse by "borrowing strength" from counts in other years. We present a model of escapement and of count data, a hierarchical Bayesian statistical framework, a Gibbs sampling approach for evaluation of the posterior distributions of the quantities of interest, and criteria for determining when the model and inference are adequate. We then apply the hierarchical Bayesian model to estimating historical escapement and escapement timing for pink salmon (Oncorhynchus gorbuscha) returns to Kadashan Creek in Southeast Alaska.


2003 ◽  
Vol 81 (12) ◽  
pp. 1986-1995 ◽  
Author(s):  
G T Crossin ◽  
S G Hinch ◽  
A P Farrell ◽  
M P Whelly ◽  
M C Healey

Pink salmon (Oncorhynchus gorbuscha) are generally considered weak upriver migrants relative to sockeye salmon (Oncorhynchus nerka), though this assertion is largely anecdotal. To assess energy-use patterns during migration, we collected pink salmon from two major Fraser River stocks (Weaver and Seton in British Columbia, Canada) in 1999 at three times and locations: (1) at the start of freshwater migration, (2) at the end of migration before spawning, and (3) immediately after spawning. We calculated the energy content of somatic and reproductive tissues, recorded several body measurements, and conducted both intraspecific (between pink stocks) and interspecific analyses with co-migrating Fraser River sockeye salmon collected during the same season. We found that between pink salmon stocks, there were no significant energetic or morphological differences either at river entry or upon arrival at spawning areas regardless of the level of migratory difficulty encountered. When compared with sockeye salmon, however, we found that pink salmon began upriver migration with significantly smaller somatic energy reserves but made up for this deficiency by minimizing absolute transport and activity costs, presumably by seeking out migratory paths of least resistance. This energetic efficiency comes at a cost to reproductive output: relative to sockeye salmon, pink salmon diverted less absolute energy to egg production, producing smaller ovaries and fewer eggs. We speculate that fundamental differences in behaviour shape the migratory energetic tactics employed by pink salmon.


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