. (2003). The effect of temperature on swimming performance and oxygen consumption in adult sockeye (Oncorhynchus nerka) and coho (O. kisutch) salmon stocks. J. Exp. Biol. 206,[3239][3240][3241][3242][3243][3244][3245][3246][3247][3248][3249][3250][3251] In both the on-line and printed versions of this paper, some of the equations in the legends to Figs 2-4 were printed incorrectly.On page 3245, in the legend to Fig.·2, the two equations should read:M O 2 routine =2.12+0.09e 0.18t (ambient; broken line) and M O 2 routine =1.39+0.54e 0.08t (adjusted; solid line).On page 3246, in the legend to Fig.·3 The authors apologise for any inconvenience these errors may have caused.Temperature has been coined the 'ecological master factor' for fish (Brett, 1971), and important physiological functions such as growth, swimming performance and active metabolic rate can have species-specific temperature optima that are near a species-preferred or acclimated temperature (Fry, 1947;Brett, 1971;Dickson and Kramer, 1971;Beamish, 1978;Houston, 1982;Bernatchez and Dodson, 1985;Johnston and Temple, 2002). Thus, when fish are exposed to temperature changes, they can obtain optimal performance by altering either their behaviour (preference/avoidance) or their physiology (adaptation and acclimation), when the temperature change is sufficiently long. Certain short-term variations in temperature may be unavoidable, however, and this is particularly the case for adult migratory salmon that are returning to their natal streams to spawn. For example, water temperatures in one of the world's greatest salmon-bearing rivers, the Fraser River, BC, Canada, may vary annually on a given date by as much as 6°C. Furthermore, the river temperatures encountered by the Early Stuart stock of Fraser River sockeye salmon Oncorhynchus nerka during its 25-day migration can vary by as much as 10.5°C (Idler and Clemens, 1959) and reach up to 22°C .Given the adult salmon's short migration window and its exposure to a wide variation in temperature, it is possible that acclimation mechanisms that would normally compensate for temperature change may be incomplete. Conversely, Guderley and Blier (1988) suggest that swimming performance and most of its components demonstrate thermal compensation on an evolutionary time scale (i.e. adaptation) such that optimal performance and lowest thermal sensitivity are typically within the temperature range most frequently encountered by the organism. In the case of adult salmon stock, the prediction is that they would retain sufficient physiological flexibility to accommodate the range of temperatures most frequently Our knowledge of the swimming capabilities and metabolic rates of adult salmon, and particularly the influence of temperature on them, is extremely limited, and yet this information is critical to understanding the remarkable upstream migrations that these fish can make. To remedy this situation, we examined the effects of temperature on swimming performance and metabolic rates of 107 adult fish taken from three sto...

Depending on population, wild Fraser River sockeye salmon Oncorhynchus nerka travel distances of <100 km to >1100 km and ascend elevations ranging from near sea-level to 1200 m to reach spawning areas. Populations embarking on distant, high elevation migrations (i.e. Early Stuart, Chilko and Horsefly populations) began their upriver spawning migrations with higher densities of somatic energy (c. 9Á2 to 9Á8 MJ kg À1) and fewer eggs (c. 3200 to 3800) than populations making shorter, low elevation migrations (i.e. Weaver and Adams; c. 7Á1 to 8Á3 MJ kg À1 gross somatic energy and c. 4300 to 4700 eggs). Populations making difficult upriver migrations also had morphologies that were smaller and more fusiform than populations making less difficult migrations, traits that may facilitate somatic energy conservation by reducing transport costs. Indeed, fish travelling long distances expended less somatic energy per unit of migratory difficulty than those travelling shorter distances (2Á8 to 3Á8 kJ v. 10-1400 kJ). Consistent with evolutionary theory, difficult migrations appear to select for energy efficiency but ultimately fish making more difficult migrations produce fewer eggs, even when differences in body length have been accounted for. Despite large among-population differences in somatic energy at the start of upriver migration, all populations completed migration and spawning, and subsequently died, with c. 4MJkg À1 of energy remaining, a level which may reflect a threshold to sustain life.

test temperature. The non-aerobic cost of swimming to Ucrit was estimated to add an additional 21.4-50.5% to the oxygen consumption measured at U crit. While these nonaerobic contributions to swimming did not affect the minimum cost of transport, they were up to three times higher than the value used previously for an energetic model of salmon migration in the Fraser River, BC, Canada. As such, the underestimate of non-aerobic swimming costs may require a reevaluation of the importance of how in-river barriers like rapids and bypass facilities at dams, and year-to-year changes in river flows and temperatures, affect energy use and hence migration success.

We evaluated the effects of past and future trends in temperature and discharge in the Fraser River on the migratory performance of the early Stuart population of sockeye salmon Oncorhynchus nerka. Fish of lower condition exhibited disproportionately higher mortality during the spawning run, elucidating a critical link between energetic condition and a fish's ability to reach the spawning grounds. We simulated spawning migrations by accounting for energetic demands for an average individual in the population from the time of entry into the Fraser River estuary to arrival on the spawning grounds (about 1,200 km upstream) and estimated energy expenditures for the average migrant during 1950-2001. The model output indicates relatively high interannual variability in migration energy use and a marked increase in energy demands in recent years related to unusually high discharges (e.g., 1997) and warmer than average water temperature (e.g., 1998). We examined how global climate change might effect discharge, water temperature, and the energy used by sockeye salmon during their spawning migration. Expected future reductions in peak flows during freshets markedly reduced transit time to the spawning ground, representing a substantial energy [Article] savings that compensated for the effect of the increased metabolic rate resulting from exposure to warmer river temperatures. We suggest that such watershed-scale compensatory mechanisms may be critical to the long-term sustainability of Pacific salmon, given expected changes in climate. However, such compensation will probably only be applicable to some stocks and may be limited under extremely high temperatures where nonenergetic factors such as disease and stress may play a more dominant role in defining mortality. Our results further indicate that a long-term decline in the mean mass of adult sockeye salmon completing their marine residency could erode their migratory fitness during the river migration and hence jeopardize the sustainability of sockeye salmon and the fishery that targets them. 656 RAND ET AL.

Since 1995, several stocks of Fraser River sockeye salmon (Oncorhynchus nerka) have begun upriver spawning migrations significantly earlier than previously observed. In some years, the timing of peak migration has shifted more than 6 weeks. Coincident with this early migration are high levels of en route and pre‐spawning mortality, occasionally exceeding 90%. These phenomena pose risks to the perpetuation of these fisheries resources. At present, although there are many competing hypotheses (e.g., energetics, osmoregulatory dysfunction, oceanic conditions, parasites) that may account for early migration and high mortality, there are no definitive answers, nor any causal evidence that link these issues. With poor predictive ability in the face of uncertainty, fisheries managers have been unable to effectively allocate harvest quotas, while ensuring that sufficient fish are able to not only reach the spawning sites, but also successfully reproduce. If trends in mortality rates continue, several important sockeye salmon fisheries and stocks could collapse. Indeed, one sockeye stock has already been emergency listed as endangered under Canadian legislation.