Logging Impacts and Some Mechanisms that Determine the Size of Spring and Summer Populations of Coho Salmon Fry (Oncorhynchus kisutch) in Carnation Creek, British Columbia

1984 ◽  
Vol 41 (7) ◽  
pp. 1097-1105 ◽  
Author(s):  
J. C. Scrivener ◽  
B. C. Andersen

Natural patterns in emergence times, seaward movements, instream distributions, densities, and growth of coho salmon fry (Oncorhynchus kisutch) between March and September are contrasted with patterns observed during and after logging in the Carnation Creek watershed. After streamside logging in 1976–77, fry emerged up to 6 wk earlier and moved seaward more quickly than during years before logging. These observations are attributed to higher water temperatures during the winter and to emergence during a period of more frequent freshets. Increased fry movement from the stream could result in habitat being underutilized. In sections affected by intense streamside logging, the deposition of "fine" logging debris led to increased fry densities during the summers of 1977 and 1978. After major freshets in November 1978, which removed this fine debris and affected channel morphology in these sections, fry densities declined below those observed prior to logging. Growth rate of fry was inversely correlated with density in all stream sections. Growth rates, after correction for density, tended to be greater in all sections after the adjacent streamside was logged. Larger fry and more variable numbers of fry remained in the stream in September after logging than before logging. Their increased size is attributed to the longer growing season afforded by earlier emergence. This complex of interacting factors determines the number and size of fry in autumn and it can influence the production of smolts the following spring.


1997 ◽  
Vol 75 (2) ◽  
pp. 335-337 ◽  
Author(s):  
Anthony P. Farrell ◽  
William Bennett ◽  
Robert H. Devlin

We examined the consequence of remarkably fast growth rates in transgenic fish, using swimming performance as a physiological fitness variable. Substantially faster growth rates were achieved by the insertion of an "all-salmon" growth hormone gene construct in transgenic coho salmon (Oncorhynchus kisutch). On an absolute speed basis, transgenic fish swam no faster at their critical swimming speed than smaller non-transgenic controls, and much slower than older non-transgenic controls of the same size. Thus, we find a marked trade-off between growth rate and swimming performance, and these results suggest that transgenic fish may be an excellent model to evaluate existing ideas regarding physiological design.



1988 ◽  
Vol 45 (6) ◽  
pp. 1036-1044 ◽  
Author(s):  
J. P. Fisher ◽  
W. G. Pearcy

Estimated growth rates, condition, and stomach fullness of juvenile coho salmon (Oncorhynchus kisutch) caught in the ocean in early summer, when mortality was most variable, were as high in 1983 and 1984, years of very low survival and low early upwelling, as in 1981, 1982, and 1985, years of higher survival and higher early upwelling. Chronic food shortage leading to starvation, poor condition, or slow growth apparently was not the cause of the increased mortality of juvenile coho salmon in 1983 and 1984. Survival of juvenile coho salmon was positively correlated with purse seine catches of fish in June and with early summer upwelling, 1981–85. Hence, year-class success probably was determined early in the summer, soon after most juvenile coho salmon entered the ocean. Spacing of the first five ocean circuli, which was positively correlated with growth rate, was not significantly different for fish caught early in the summer and those caught late in the summer, suggesting that growth rate selective mortality in the ocean was not strong. The increase in mortality in 1983 and 1984 may have been caused by increased predation on juvenile coho salmon due to decreased numbers of alternative prey for predators.



1990 ◽  
Vol 47 (5) ◽  
pp. 852-861 ◽  
Author(s):  
C. S. Shirvell

Coho salmon fry (Oncorhynchus kisutch) and steelhead parr (O. mykiss) occupied previously infrequently-used mid-channel areas of Kloiya Creek, British Columbia, Canada, once artificial rootwads were placed there. Ninetynine percent of all coho salmon fry and 83% of steelhead parr occupied positions downstream of natural or artificial rootwads during artificially created drought, normal, and flood streamflows. Fish associated with rootwads regardless of distance from shore, but steelhead parr preferred rootwads away from shore while coho salmon fry preferred rootwads next to shore. Coho salmon fry increased their use of natural rootwads where currents were slow during floods, while steelhead parr increased their use of artificial and natural rootwads where light remained low during droughts. Young fish apparently selected areas having slower water 80% of the time because they provided shelter from adverse current, and areas having reduced light intensities 20% of the time because they provided protection from predators, juvenile coho salmon and steelhead in Kloiya Creek selected locations with slower water velocities and reduced light intensities irrespective of the physical structure that caused them.



1988 ◽  
Vol 45 (3) ◽  
pp. 502-515 ◽  
Author(s):  
L. Blair Holtby

Clear-cut logging of 41% of the basin of Carnation Creek, British Columbia, resulted in increased stream temperatures in all months of the year, increases above prelogging temperatures ranged from 0.7 °C in December to 3.2 °C in August. Earlier emergence of coho salmon (Oncorhynchus kisutch) fry associated with the temperature increases lengthened their summer growing season by up to 6 wk. Fingerlings were significantly larger by the fall in the years after logging compared with the years before logging. The increased size of fingerlings was associated with improved overwinter survival. Following logging, yearling smolt numbers doubled, although 2-yr-old smolt numbers decreased. Warmer spring temperatures were also associated with earlier seaward migration of smolts, probably resulting in decreased smolt-to-aduit survivals. A linked series of models that first predict logging effects on stream temperatures and then the effects of those temperatures on critical coho life history events are developed. The life history model is used to quantify the effects of stream temperature changes related to logging on the population size of adult coho salmon. The predicted effect of those temperature changes was a 9% increase in adult coho numbers prior to the fishery, an increase considerably less than the observed 47% increase in smolt numbers.



1989 ◽  
Vol 46 (8) ◽  
pp. 1396-1405 ◽  
Author(s):  
L. Blair Holtby ◽  
Thomas E. McMahon ◽  
J. Charles Scrivener

Variability in average stream temperatures between peak spawning and fry emergence accounted for 82 and 77% of the variance in the median emigration date of fry of chum (Oncorhynchus keta) and coho salmon (O. kisutch) respectively over a 9 to 10-yr period. The modeled relationships were indistinguishable from laboratory models that predicted time to maximum alevin wet weight. Variability in stream temperatures during the spring accounted for 60% of the variability in the median date of coho smolt emigration. As stream temperatures increased, the predicted thermal summations required for emigration were nearly constant for coho salmon fry, increased moderately for chum salmon fry and increased strongly for coho salmon smolts The duration of the emigration period also differed between the groups: 50% of the chum salmon fry emigrated over a 1-wk period compared with a 2- to 3-wk period for coho salmon fry and smolts. We speculate that the emigration timing —temperature relationships and timing of adult spawning represent adaptations for synchronizing emigration with "windows of opportunity" in the ocean or stream. The windows are of different widths and levels of predictability for coho and chum salmon fry and coho salmon smolts.



1983 ◽  
Vol 61 (5) ◽  
pp. 1120-1127 ◽  
Author(s):  
L. M. Carl

Coho salmon spawning peaked in the late fall. Spawning densities ranged from fewer than 5 coho salmon per hectare up to 90 fish per hectare. Subyearling coho salmon densities ranged from 10 to 60 fish per 100 m2 in June and dropped to 5–20 fish by early fall. Coho salmon fry increased in length from 40 mm in early May, to over 120 mm by smolt out-migration in the following April. Coho salmon instantaneous daily change in density coefficients ranged from 0.004 to 0.019 and were dependent on initial coho density. Daily coho salmon growth rates ranged from 0.38 to 0.60 mm per day and were not dependent on initial coho salmon density. Downstream movement of rainbow trout fry began in May, and continued into July. In the spring 10–20 yearlings and one to five 2-year-olds per 100 m2 were present. Most fry emerged in June at a size of 25 mm and grew to 85 mm by fall. Daily growth rates varied from 0.23 to 0.45 mm per day for yearling rainbow trout and were not correlated with rainbow trout density.



1978 ◽  
Vol 14 (1) ◽  
pp. 1-5 ◽  
Author(s):  
J. L. Monteith

SUMMARYFigures for maximum crop growth rates, reviewed by Gifford (1974), suggest that the productivity of C3 and C4 species is almost indistinguishable. However, close inspection of these figures at source and correspondence with several authors revealed a number of errors. When all unreliable figures were discarded, the maximum growth rate for C3 stands fell in the range 34–39 g m−2 d−1 compared with 50–54 g m−2 d−1 for C4 stands. Maximum growth rates averaged over the whole growing season showed a similar difference: 13 g m−2 d−1 for C3 and 22 g m−2 d−1 for C4. These figures correspond to photosynthetic efficiencies of approximately 1·4 and 2·0%.



2017 ◽  
Vol 130 (4) ◽  
pp. 336 ◽  
Author(s):  
Eric A Parkinson ◽  
Chris J Perrin ◽  
Daniel Ramos-Espinoza ◽  
Eric B Taylor

The Coho Salmon, Oncorhynchus kisutch, is one of seven species of Pacific salmon and trout native to northeastern Pacific Ocean watersheds. The species is typically anadromous; adults reproduce in fresh water where juveniles reside for 1–2 years before seaward migration after which the majority of growth occurs in the ocean before maturation at 2–4 years old when adults return to fresh water to spawn. Here, we report maturation of Coho Salmon in two freshwater lakes on the north coast of British Columbia apparently without their being to sea. A total of 15 mature fish (11 males and four females) were collected in two lakes across two years. The mature fish were all at least 29 cm in total length and ranged in age from three to five years old. The occurrence of Coho Salmon that have matured in fresh water without first going to sea is exceedingly rare in their natural range, especially for females. Such mature Coho Salmon may represent residual and distinct breeding populations from those in adjacent streams. Alternatively, they may result from the ephemeral restriction in the opportunity to migrate seaward owing to low water levels in the spring when Coho Salmon typically migrate to sea after 1–2 years in fresh water. Regardless of their origin, the ability to mature in fresh water without seaward migration may represent important adaptive life history plasticity in response to variable environments.



1986 ◽  
Vol 64 (1) ◽  
pp. 84-87 ◽  
Author(s):  
Thomas P. Quinn ◽  
Graeme M. Tolson

To test the hypothesis that population-specific pheromones guide adult salmonids to their natal streams, juvenile and adult coho salmon (Oncorhynchus kisutch) were tested for chemosensory responses in two-choice tanks. Coho salmon from Quinsam and Big Qualicum rivers, British Columbia, Canada, distinguished their own population from the other. Tagging evidence indicates that straying between these two rivers and a third, geographically intermediate river seldom occurs. Thus, population-specific chemicals constitute a potential source of information for homing coho salmon, though their role vis-à-vis imprinted odors from other sources could not be evaluated.



1976 ◽  
Vol 33 (7) ◽  
pp. 1585-1603 ◽  
Author(s):  
David A. Higgs ◽  
Edward M. Donaldson ◽  
Helen M. Dye ◽  
J. R. McBride

Groups of underyearling coho salmon (Oncorhynchus kisutch) were acclimated to 10 C well water and a photoperiod of 12 h L:12 h D. Excess ration (Oregon Moist Pellet) was presented daily. Doses of bovine growth hormone (5, 10, 20, 30, or 90 μg bGH/g body wt) and L-thyroxine (0.5, 5, or 30 μg T4/g) were administered over a period of 84 days (phase I) either by injection (via dorsal musculature or peritoneal cavity) or by hormone cholesterol implants into the muscle. Administration frequency of bGH and T4 was such (range 2 times/wk-1 time/3 wk) that fish theoretically received either 10 or 30 μg bGH/g per wk or 1 or 10 μg T4/g per wk. Control fish received either alkaline saline (pH 9.5) or a cholesterol pellet. After cessation of treatment the fish were observed for an additional 84 days (phase II). During phase I, growth rates (weight) for bGH fish (2.0–2.4% per day) and for T4 fish (0.97–1.1% per day) were significantly higher than those of control fish (0.42–0.59% per day). Among bGH fish, dorsal musculature injection (2 times/wk) was significantly more effective than intraperitoneal injection (1 time/2 wk).Increases in weight above control for bGH fish at 84 days ranged from 220 to 369%. Those for T4 fish extended from 47 to 78%. In phase II, control fish growth rates were higher (0.61–0.67% per day) than those for bGH fish (0.47–0.57% per day) and T4 fish (0.32–0.44% per day). Administration of bGH and T4 (high dose) caused a progressive decline in condition factor of fish from the control range. This trend was stopped and reversed in phase II.At 84 days, generally no significant differences were detected among groups for percentages of muscle water. However, some groups had significantly higher (bGH) and others lower (T4) percentages of muscle protein relative to those of control fish. Also, significant increases (T4) and decreases (bGH) in muscle lipid percentages were found. Hormone treatment altered the histological structure of the ovary, thyroid, exocrine (T4) and endocrine (bGH) pancreas, and somatotrop cells (T4) of the pituitary. A poor growth response was noted for two groups of coho administered bGH after acclimation to sea water.



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