Density-Dependent, Trophic Level Responses to an Introduced Run of Sockeye Salmon (Oncorhynchus nerka) at Frazer Lake, Kodiak Island, Alaska

1988 ◽  
Vol 45 (5) ◽  
pp. 856-867 ◽  
Author(s):  
G. B. Kyle ◽  
J. P. Koenings ◽  
B. M. Barrett

Sockeye salmon (Oncorhynchus nerka) have developed into a major run at Frazer Lake, Kodiak Island, Alaska, reaching over 600 000 adults 34 yr after the first egg-plant in 1951. In the last nine years (1978–86), escapements have averaged over 250 000 with a record high of 486 000 adults in 1985. The increase in escapements were inversely related to seasonal macrozooplankton densities (p < 0.05; r2 = 0.42) but directly correlated with increases in the cladoceran to copepod ratio (p < 0.001). In addition, the average body length of the smallest macrozooplanker (Bosmina) has shifted below the observed threshold length of 0.40 mm for juvenile sockeye prey. We also found an inverse relationship between greater parental escapements and age 1. smolt length (p < 0.01; r2 = 0.75). Small-sized smolts produced from a density-dependent rearing environment indicate that spawning capacity equals or exceeds rearing capacity. Juvenile recruits from larger escapements (~400 000) exerted a controlling, density-dependent influence on the secondary trophic level which drastically reduced subsequent adult returns. Moreover, adverse trophic level changes, particularly after the largest escapements, also appeared to reduce the rearing efficiency for lower densities of juveniles, as subsequent smolt sizes from smaller escapements were less than expected. Thus, these findings not only provide a rationale for suggesting that fewer spawners would provide recruits more closely matching the rearing capacity of this lake, but also provide empirical evidence for the potential adverse density-dependent effects of large escapements.

1979 ◽  
Vol 36 (10) ◽  
pp. 1265-1277 ◽  
Author(s):  
R. F. Blackett

Runs of sockeye salmon (Oncorhynchus nerka) and chinook salmon (O. tshawytscha) were established at Frazer Lake, Kodiak Island, Alaska by adult spawner transplants, fry plants, and eyed-egg plants. Falls in the lake outlet formed a barrier to natural ascent of anadromous fish until construction of a fishpass in 1962. Accounts of successful introduction and development of viable and self-sustaining runs of salmon where none previously existed and the lake was inaccessible are scarce in the history of salmon fisheries on the Pacific Coast. The first sockeye returning to Frazer Lake in 1956 were produced from egg plants in 1951. Annual sockeye returns have progressively increased over a 28-yr period reaching record passage of 141 981 in 1978. Sockeye spawning has extended into new areas as returns increased. Spawning area capacity is projected to be sufficient for 365 000 sockeye while rearing area is estimated to be sufficient to support fry production from 400 000 sockeye. Sockeye returns per spawner have averaged 3.2 for six parent years (1966–71) in which returns are complete. A chinook run was created from plants of 160 000 fry over a 4-yr period beginning in 1966. Chinook have returned to spawn in specific sites of fry release above the falls and in the lower river. Key words: salmon introduction, enhancement technique, sockeye, chinook, Frazer Lake, salmon establishment


2004 ◽  
Vol 61 (1) ◽  
pp. 80-92 ◽  
Author(s):  
Lucy Flynn ◽  
Ray Hilborn

In this paper, we explore sources of variability in test fishing indices for sockeye salmon (Oncorhynchus nerka) and illustrate potential solutions. For our analysis, we use the Port Moller test fishery in Bristol Bay, Alaska. The traditional model used to forecast run size using Port Moller test fishery data is based on a simple linear regression of total returns to the fishing districts against the cumulative test fishery catch-per-unit-effort (CPUE) index on a given date. We show that much of the inaccuracy of recent forecasts based on test fishery indices is due to the variable age composition of sockeye runs and the unequal vulnerability of respective age classes to the test fishing gear. We also illustrate solutions to the problems presented by variability in migration route and variability in return timing. In warmer years, we found that there was an increase in effective vulnerability to the test fishing gear and that the strength of this relationship increased linearly with the average body length of age classes. Retrospective analysis shows that correcting for age composition, migration route, and timing provides an in-season index of abundance with an average error of 6.7 million fish or 21%, compared with 33% for previous models.


2003 ◽  
Vol 60 (5) ◽  
pp. 553-562 ◽  
Author(s):  
T P Quinn ◽  
S M Gende ◽  
G T Ruggerone ◽  
D E Rogers

The number of sockeye salmon (Oncorhynchus nerka) killed by brown bears (Ursus arctos) in 13 streams over more than a decade in southwestern Alaska was best explained by an asymptotic increase to about 3000 salmon killed per stream per year as salmon density increased to 10 000 fish·ha–1 of stream. Divergence from this pattern at some streams probably reflected variation in the number of bears using the stream (which we did not determine) and variation in salmon biomass consumed per fish killed. Daily surveys at one creek over 11 years revealed about 100–130 salmon killed per day, ranging from a few to over 600. Higher proportions of the available salmon were killed early and late in the season, when densities were low. Thus the number of salmon killed within and among years increased with salmon abundance but at a declining rate, and the proportion killed generally decreased. Our previous work indicated that the average proportion of salmon killed among streams was controlled mostly by stream size, affecting the ability of bears to catch salmon. These findings are important for understanding the effects of bears on salmon population dynamics and their role in the transport of nutrients from salmon carcasses.


1997 ◽  
Vol 54 (10) ◽  
pp. 2449-2462 ◽  
Author(s):  
R A Myers ◽  
M J Bradford ◽  
J M Bridson ◽  
G Mertz

Delayed density-dependent mortality can be a cause of the cyclic patterns in abundance observed in many populations of sockeye salmon (Oncorhynchus nerka). We used a meta-analytical approach to test for delayed density dependence using 34 time series of sockeye data. We found no consistent evidence for delayed density-dependent mortality using spawner - spring fry or spawner-recruit data. We did find evidence for delayed density-dependent mortality at a 1 year lag for the spawner - fall fry and the spawner-smolt data; however, effects at lags greater than 1 year were weak and not statistically significant. Between-cohort interactions at a 1-year lag are not sufficient to cause the observed cycles in adult abundance, although they will tend to reinforce patterns established by other mechanisms. Our results imply that reductions in fishing mortality in off-peak years should result in an increase in abundance.


1987 ◽  
Vol 44 (1) ◽  
pp. 66-76 ◽  
Author(s):  
Roger F. Blackett

A major introduced run of sockeye salmon (Oncorhynchus nerka) at Frazer Lake, Kodiak Island, Alaska, is perpetuated by an Alaska steeppass fishway at a 10-m-high falls on the outlet river. Experimental modifications of the fishway, which was inadequate by 1970 as the salmon run increased, improved salmon entry and passage. Sockeye passage over 4 yr was nearly equivalent in a steeppass of 60 m continuous length (22% slope) and an adjoining steeppass with three resting pools, but significant year-to-year differences in passage occurred between steeppasses. Resting tanks were beneficial for holding slower or descending salmon without blocking passage of other salmon. An average entry of 142 sockeye in 15 min was achieved by guiding all salmon along a weir to an entrance tank with a vertical slot orifice. Chutes installed in the entry end of the steeppasses created a high-velocity stream for attraction and decreased salmon dropout from the entrance tank. Salmon passage in the original steeppasses with three resting pools was greater than in new (1979) steeppasses with a single resting pool. In 1985, sockeye passage of 2925/h and 46 806/d exceeded fishway capacity requirements.


1976 ◽  
Vol 33 (1) ◽  
pp. 186-188 ◽  
Author(s):  
Roger S. Grischkowsky ◽  
Donald F. Amend

Infectious hematopoietic necrosis (IHN) virus is reported for the first time in Alaskan sockeye salmon (Oncorhynchus nerka). The virus was isolated from moribund juveniles at Kitoi Bay and from adults of 16 spawning stocks throughout the Bristol Bay, Kodiak Island, Cook Inlet, and the Gulf of Alaska areas.


1984 ◽  
Vol 41 (12) ◽  
pp. 1825-1829 ◽  
Author(s):  
Randall M. Peterman

Significant decreases in adult body size and marine growth rate occur in seven British Columbia and Bristol Bay, Alaska, sockeye salmon (Oncorhynchus nerka) stocks when large numbers of sockeye are present in the Gulf of Alaska. These density-dependent effects arise mainly during early ocean life and are probably due to competition for food. The total sockeye abundance in the Gulf of Alaska is at least as important as within-stock abundance in determining final adult body size. British Columbia sockeye show a 10–22% decrease in adult body weight at high abundance of conspecifics. Thus, future evaluations of management strategies cannot simply focus on individual stocks, but must take a broader perspective which includes other sockeye populations.


Author(s):  
Thomas P. Quinn ◽  
George R. Pess ◽  
Ben J.G. Sutherland ◽  
Samuel J. Brenkman ◽  
Ruth E. Withler ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document