Spatiotemporal patterns in migration timing of coho salmon (Oncorhynchus kisutch) smolts in North America

2010 ◽  
Vol 67 (8) ◽  
pp. 1316-1334 ◽  
Author(s):  
Brian C. Spence ◽  
James D. Hall

The timing of ocean entry by salmon smolts is presumed adaptive to maximize survival during this critical life transition. We analyzed the peak timing, duration, and interannual variation in timing of smolt migrations for 53 coho salmon ( Oncorhynchus kisutch ) populations from central California to Kodiak Island, Alaska. The objective was to examine potential influences of both local watershed characteristics and larger-scale processes in the marine environment on smolt migration patterns. Multivariate analyses demonstrated a strong latitudinal gradient in migration patterns with trends toward later, shorter, and more predictable migrations with increasing latitude. Cluster analysis performed on migration descriptors indicated three major population groupings that coincide with major coastal oceanic regions in the northeast Pacific: a northern group from Kodiak Island to the Queen Charlotte Islands, British Columbia, a central group from the Queen Charlotte Islands south to the Columbia River, and a southern group from the Columbia River southward. These regional patterns transcended local variability associated with watershed characteristics and trap location, suggesting that the patterns reflect adaptation to differences in timing and relative predictability of favorable conditions in the marine environments that smolts enter.

1982 ◽  
Vol 60 (6) ◽  
pp. 1463-1469 ◽  
Author(s):  
Terry D. Beacham

Significant regional and annual variability in fecundity of coho salmon (Oncorhynchus kisutch) and chum salmon (O. keta) in British Columbia was detected during this investigation. A Kodiak Island (Alaska) coho salmon stock was more fecund than southern stocks in British Columbia and Washington. Fecundity ranged from 2450 to 2850 eggs per female at 53.6 cm postorbital–hypural length for Vancouver Island stocks to over 4400 eggs per female for a Kodiak Island stock at the same length. Chum stocks on Vancouver Island and the Queen Charlotte Islands generally had fecundities less than 3200 eggs per female at 58.8 cm postorbital–hypural length, whereas chum of equal lengths in mainland British Columbia stocks ranged from 3200 to 3450 eggs per female. Older chum and coho were usually more fecund than younger ones, but this difference could be accounted for by differences in mean length-at-age, fecundity being related to body size.


1990 ◽  
Vol 68 (2) ◽  
pp. 347-358 ◽  
Author(s):  
C. B. Murray ◽  
T. D. Beacham ◽  
J. D. McPhail

Coho salmon (Oncorhynchus kisutch) stocks in British Columbia spawning from October to April were surveyed for variation in developmental characteristics at incubation temperatures from 1.5 to 15 °C. There were no trends in embryo or alevin survival rates associated with spawning time or spawning temperature. The highest embryo and alevin survival rates occurred at 4 or 5 °C and complete mortality generally occurred at 14 or 15 °C. Vancouver and Queen Charlotte Island stocks had lower survival rates at 1.5 and 2 °C than did mainland stocks. Time to 50% hatching and 50% emergence varied inversely with incubation temperature. Alevin hatching time for the Pallant Creek stock on the Queen Charlotte Islands was later than for all other stocks. Stocks had different trends in alevin and fry length and weight with respect to incubation temperature. Northern stocks tended to be more efficient than southern stocks at converting yolk to body tissue at 1.5 and 2 °C, as were mainland stocks compared with island stocks.


2001 ◽  
Vol 58 (7) ◽  
pp. 1453-1463 ◽  
Author(s):  
Rishi Sharma ◽  
Ray Hilborn

We assembled data on coho salmon (Oncorhynchus kisutch) from 14 streams in western Washington, including annual smolt counts and annual escapement, either as absolute counts or as an index. We also compiled data on large woody debris (number·km%#150;1 of stream), road densities in the watersheds (km road·km%#150;2), gradient of the streams (%), valley slope adjacent to the stream (%), drainage area in the watershed (km2), and pool, pond, and lake areas (m2·km%#150;1). We explored the relationships between habitat variables and two measures of coho production, the maximum production of smolts in the stream (capacity) and the maximum smolts/spawner (productivity). Using the 11 streams with pool and pond counts, we found that pool and pond densities served as good predictors of smolt density (r2 = 0.85 for pools and 0.68 for ponds, independently). Pools produced 0.39 smolts·m%#150;2 and ponds produced 0.07 smolts·m%#150;2 in the multiple regression fit, accounting for 92% of the residual error. We also found that lower valley slopes, lower road densities, and lower stream gradients were correlated with higher smolt density.


1970 ◽  
Vol 27 (12) ◽  
pp. 2371-2373 ◽  
Author(s):  
Fred M. Utter ◽  
Warren E. Ames ◽  
Harold O. Hodgins

Six transferrin phenotypes observed in sera of coho salmon (Oncorhynchus kisutch) were interpreted as a reflection of three alleles — TfA, TfB, and TfC — at a single locus. The distribution of these alleles differed significantly among samples collected from streams entering Puget Sound and tributaries of the Columbia River, suggesting a potential usefulness of this system for stock identification.


2014 ◽  
Vol 71 (1) ◽  
pp. 56-69 ◽  
Author(s):  
Brian C. Spence ◽  
E.J. Dick

The environmental cues that regulate smoltification and trigger downstream movement by salmon should vary across space in response to differences in the predictability of favorable conditions for migration and ocean entry. To examine this, we modeled the short-term outmigration probability of four coho salmon (Oncorhynchus kisutch) populations in three distinct geographic regions in relation to photoperiod, temperature, streamflow, lunar phase, and interactions among these variables. For smolts in Deer and Flynn creeks, Oregon (1960–1972), migration probability was influenced by numerous factors, including photoperiod, temperature (absolute and change), flow (absolute and change), and lunar phase, with certain factors interacting. Smolts from Carnation Creek, British Columbia (1972–1986) responded to a similarly diverse suite of factors (excluding lunar phase), though in somewhat different ways. In contrast, migration timing of smolts in Sashin Creek, Alaska (1959–1969) was best explained by a model that included only photoperiod, temperature, and the interaction between these terms. These population differences suggest fundamental differences across regions in the selection processes operating in both marine and freshwater environments.


1991 ◽  
Vol 48 (2) ◽  
pp. 248-253 ◽  
Author(s):  
Mario F. Solazzi ◽  
Thomas E. Nickelson ◽  
Steven L. Johnson

We released six groups of marked yearling hatchery coho salmon (Oncorhynchus kisutch) in six locations each year for five years beginning with the 1981 brood. Fish were released immediately below Bonneville Dam (control), at the Tongue Point Coast Guard Station (head of saltwater intrusion in the Columbia River), between the jetties at the Columbia River bar, in the Columbia River plume water, in coastal water approximately 19 km north and 19 km offshore of the mouth of the river, and in oceanic water approximately 38 km offshore. We found a 1.6-fold increase in the survival index (ocean catch through September 18 each year) for the fish released at Tongue Point compared with the control group. After adjusting for differences in the survival index between release groups, we found a 2.5-fold increase in the contribution to the Columbia River gillnet fishery from the fish released at Tongue Point compared with the control group. We found no significant difference between survival of the other release groups and survival of the control group. We also found that the percentage of adult fish that returned to locations other than the Columbia basin increased as the distance the fish were transported offshore increased.


Aquaculture ◽  
1982 ◽  
Vol 28 (1-2) ◽  
pp. 251-268 ◽  
Author(s):  
Conrad Mahnken ◽  
Earl Prentice ◽  
William Waknitz ◽  
Gerald Monan ◽  
Carl Sims ◽  
...  

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