The relationships between fish health, metabolic rate, swimming performance and recovery in return-run sockeye salmon, Oncorhynchus nerka (Walbaum)

2004 ◽  
Vol 27 (11) ◽  
pp. 663-671 ◽  
Author(s):  
K B Tierney ◽  
A P Farrell
Keyword(s):  
Metabolic Rate ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Fish Health

Temperature effects on swimming performance, energetics, and aerobic capacities of mature adult pink salmon (Oncorhynchus gorbuscha) compared with those of sockeye salmon (Oncorhynchus nerka)

2006 ◽  
Vol 84 (1) ◽  
pp. 88-97 ◽  
Author(s):  
Meaghan J MacNutt ◽  
Scott G Hinch ◽  
Chris G Lee ◽  
James R Phibbs ◽  
Andrew G Lotto ◽  
...  
Keyword(s):  
Metabolic Rate ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Pink Salmon ◽  
Oncorhynchus Gorbuscha ◽  
Thermal Dependence ◽  
Cost Of Transport ◽  
Mature Adult ◽  
Pink Salmon Oncorhynchus Gorbuscha

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.

Metabolic rates and swimming performance of adult Fraser River sockeye salmon (Oncorhynchus nerka) after a controlled infection with Parvicapsula minibicornis

2005 ◽  
Vol 62 (9) ◽  
pp. 2124-2133 ◽  
Author(s):  
G N Wagner ◽  
S G Hinch ◽  
L J Kuchel ◽  
A Lotto ◽  
S RM Jones ◽  
...  
Keyword(s):  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Kidney Tissue ◽  
Severe Infection ◽  
Polymerase Chain Reaction Analysis ◽  
Infected Fish ◽  
Fraser River ◽  
Metabolic Rates ◽  
Holding Period

Adult sockeye salmon (Oncorhynchus nerka) acquire infections with the myxosporean kidney parasite Parvicapsula minibicornis during their spawning migration in the Fraser River, British Columbia. Controlled infections with this parasite in wild sockeye salmon had no significant impact on plasma ionic status, metabolic rates, and initial maximum prolonged swimming performance (Ucrit) for fish ranked as either strongly, weakly, or noninfected by polymerase chain reaction analysis of kidney tissue. However, strongly infected fish had significantly lower second Ucrit and recovery ratio (8%) values, indicating decreased ability to recover from exercise. As the present study shows that the severity of infection is affected by time and temperature, the accumulated thermal units (ATU) of exposure in this study were compared with those experienced by naturally migrating sockeye salmon. A parallel telemetry study revealed that early-timed sockeye experienced significantly more ATU (741.4 ± 29.4 °C) than normally migrating salmon (436.0 ± 20.0 °C) prior to spawning because of a significantly longer holding period in the lake system. The present data are discussed in the context of a threshold of >450 °C ATU for severe infection that would first manifest in early-timed fish in the upper reaches of the Fraser River and certainly on the spawning grounds.

Effects of Sublethal Concentrations of Sodium Pentachlorophenate on Growth Rate, Food Conversion Efficiency, and Swimming Performance in Underyearling Sockeye Salmon (Oncorhynchus nerka)

1973 ◽  
Vol 30 (4) ◽  
pp. 499-507 ◽  
Author(s):  
P. W. Webb ◽  
J. R. Brett
Keyword(s):  
Growth Rate ◽  
Conversion Efficiency ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Dry Weight ◽  
Food Conversion ◽  
Ration Level ◽  
Sodium Pentachlorophenate ◽  
Sublethal Concentrations

Tests were performed at 15 C, pH 6.8, and dissolved oxygen values of 90–100% air saturation. Growth rate and conversion efficiency were measured by feeding a ration level of 15% body dry weight/day to underyearling sockeye salmon (Oncorhynchus nerka) held at sodium pentachlorophenate (PCP) concentrations of 0, 1.14, 1.99, 3.49, 7.16, 13.60, 27.73, 31.57, and 47.18 ppb. Swimming performance was measured at PCP concentrations of 0, 7.21, 19.00, and 50.00 ppb. The 96-hr LC50 was 63 ppb PCP. Growth rate and conversion efficiency were almost equally affected by PCP, the EC50 values being 1.74 ppb for growth rate and 1.80 ppb for conversion efficiency. This is approximately 2.8% of the 96-hr LC50. Swimming performance was unaffected by PCP at the concentrations used.

Metabolic Rates and Critical Swimming Speeds of Sockeye Salmon (Oncorhynchus nerka) in Relation to Size and Temperature

1973 ◽  
Vol 30 (3) ◽  
pp. 379-387 ◽  
Author(s):  
J. R. Brett ◽  
N. R. Glass
Keyword(s):  
Metabolic Rate ◽  
Temperature Effect ◽  
Sockeye Salmon ◽  
Oncorhynchus Nerka ◽  
Standard Metabolic Rate ◽  
Metabolic Rates ◽  
Supplementary Data ◽  
B Values ◽  
Active Metabolism ◽  
Standard Metabolism

Ten years research on metabolic rates and swimming speeds of sockeye salmon (Oncorhynchus nerka) ranging in weight from 2 to 2000 g, at temperatures from 2 to 24 C, is reviewed and summarized. Analysis of weight–slope relations (b values) at three temperatures, using log–log transformations, provided an overall mean of 0.88 for standard metabolism and 0.99 for active metabolism. A previously determined semilog equation for temperature effect on standard metabolic rate (at approximately 50 g) was supported by supplementary data at 2 C. Predictive graphic models in the form of isopleths of metabolic rates and critical swimming speeds in relation to weight, length, and temperature are depicted. These provide a composite presentation useful in estimating the metabolic rate and maximum sustained speed for any size and temperature.

The Relation of Size to Rate of Oxygen Consumption and Sustained Swimming Speed of Sockeye Salmon (Oncorhynchus nerka)

1965 ◽  
Vol 22 (6) ◽  
pp. 1491-1501 ◽  
Author(s):  
J. R. Brett
Keyword(s):  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Swimming Speed ◽  
Sockeye Salmon ◽  
Oncorhynchus Nerka ◽  
Rapid Decrease ◽  
Relative Performance ◽  
Continuous Change ◽  
A Value ◽  
Rate Of Oxygen Consumption

The relation of size (log weight, g) to metabolic rate (log O2-uptake, mg O2/hr) of sockeye salmon was found to have a continuous change in slope (0.78–0.97) with increasing activity at 15 C.The slope of the equation relating the 60-min sustained swimming speed (log speed, cm/sec) to length (cm) had a value of 0.50, demonstrating a rapid decrease in relative performance with increasing size.

Does among-population variation in burst swimming performance of sockeye salmon Oncorhynchus nerka fry reflect early life migrations?

2013 ◽  
Vol 83 (5) ◽  
pp. 1416-1424 ◽  
Author(s):  
N. M. Sopinka ◽  
S. G. Hinch ◽  
A. G. Lotto ◽  
C. K. Whitney ◽  
D. A. Patterson
Keyword(s):  
Early Life ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Population Variation ◽  
Burst Swimming

scholarly journals Prolonged swimming, recovery and repeat swimming performance of mature sockeye salmon Oncorhynchus nerka exposed to moderate hypoxia and pentachlorophenol.

1998 ◽  
Vol 201 (14) ◽  
pp. 2183-2193 ◽  
Author(s):  
A P Farrell ◽  
A K Gamperl ◽  
I K Birtwell
Keyword(s):  
Oxygen Consumption ◽  
Swimming Speed ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
High Plasma ◽  
Plasma Lactate ◽  
Critical Swimming Speed ◽  
Moderate Hypoxia ◽  
Lactate Levels

Mature, wild sockeye salmon (Oncorhynchus nerka) demonstrated their remarkable stamina and recovery abilities by performing three consecutive critical swimming speed tests with only a 45 min interval for recovery between subsequent tests. Although the repeated swimming challenges were performed without a full recovery, normoxic fish swam just as well on the second swim, and the majority of fish swam only marginally more poorly on the third swim. In addition, metabolic loading in these fish, as measured by the rate of oxygen consumption, ventilation rate and plasma lactate levels during recovery, did not appear to be cumulative with successive swims. Fish, however, did not recover as well after a similar level of initial swimming performance under moderately hypoxic conditions (water PO2>100 mmHg; 1 mmHg=0.1333 kPa). Four out of the five fish did not swim again and their high plasma lactate levels indicated a greater anaerobic effort. In another group of fish, metabolic loading (elevated control rates of oxygen consumption) was induced with an overnight sublethal exposure to pentachlorophenol, but these fish swam as well as normoxic fish on the first swim, and five of the six fish swam for a third time at a marginally lower critical swimming speed. In contrast to expectations, pentachlorophenol pretreatment and moderate hypoxia were not additive in their effects. Instead, the effects resembled those of pentachlorophenol pretreatment alone. The results are discussed in terms of what aspects of fatigue might impair the repeat swimming performance of sockeye salmon.

Repeat swimming performance of mature sockeye salmon following a brief recovery period: a proposed measure of fish health and water quality

1998 ◽  
Vol 76 (8) ◽  
pp. 1488-1496 ◽  
Author(s):  
K E Jain ◽  
I K Birtwell ◽  
A P Farrell
Keyword(s):  
Sockeye Salmon ◽  
Swimming Performance ◽  
Recovery Period ◽  
Lactate Concentration ◽  
Dehydroabietic Acid ◽  
Environmental Stressors ◽  
Control Fish ◽  
Fish Health ◽  
Physical Status ◽  
Plasma Lactate Concentration

Measurements of swimming ability, such as critical swimming speed (Ucrit), have commonly been used as indicators of the effects of environmental challenges on the general health of fish. In this study, we introduce repeat swimming performance as a particularly sensitive means to assess fish health and the effects of environmental stressors. Adult sockeye salmon (Oncorhynchus nerka) performed two Ucrit tests separated by a 40-min recovery period. When recovery ability was expressed as a ratio of Ucrit values in the first and second swim challenges (Ucrit,2/Ucrit,1), control fish exhibited recovery ratios of unity (0.98 ± 0.01 (mean ± SEM)). In contrast, the recovery of fish pre-exposed to between 0.12 and 0.77 mg·L-1 dehydroabietic acid (DHA) for 8-14 h, and swimming in either hypoxia or normoxia, was impaired. These fish had recovery ratios significantly lower than unity (0.92 ± 0.02) despite swimming to a similar initial Ucrit as control fish. The effect of pre-exposure to DHA was also evident in measurements of oxygen consumption and plasma lactate concentration. Unhealthy fish exhibited significantly lower initial and second Ucrit values than control fish. To account for the low initial swimming performance of these fish, a normalized recovery ratio was introduced ((Ucrit,1/Ucrit,1(control) + Ucrit,2/Ucrit,1)/2). This index of recovery (0.65 ± 0.08) identified the poor physical status of these fish.

Effects of Eubothrium salvelini (Cestoda: Pseudophyllidea) on the growth and vitality of sockeye salmon, Oncorhynchus nerka

1979 ◽  
Vol 57 (3) ◽  
pp. 597-602 ◽  
Author(s):  
N. P. Boyce
Keyword(s):  
Deleterious Effect ◽  
Sockeye Salmon ◽  
Swimming Performance ◽  
Oncorhynchus Nerka

Sockeye salmon (Oncorhynchus nerka) fry infected experimentally with the cestode Eubothrium salvelini, as well as noninfected controls, were studied in the laboratory for approximately 1 year through their development to the smolt stage. Fish were weighed and measured at 10-day intervals and tested for stamina in an active capacity tunnel. Parasitism had a deleterious effect on the growth, survival, and swimming performance of the fish.

Respiratory Metabolism and Swimming Performance of the Squid, Loligo opalescens

1982 ◽  
Vol 39 (4) ◽  
pp. 580-587 ◽  
Author(s):  
R. K. O'Dor
Keyword(s):  
High Speed ◽  
Sockeye Salmon ◽  
Large Scale ◽  
Swimming Performance ◽  
Oncorhynchus Nerka ◽  
Oxygen Debt ◽  
Cost Of Transport ◽  
Loligo Opalescens ◽  
Single Jet ◽  
Low Efficiency

Maximum sustainable and burst speed, standard and active metabolic rates, and metabolic scope at temperatures from 7.5 to 17.5 °C were determined for the squid, Loligo opalescens, with a Brett tunnel respirometer. A comparison with sockeye salmon (Oncorhynchus nerka) of similar size at 15 °C indicates that squid have higher standard and active rates (254 and 862 mL O2∙kg−1∙h−1), but have sustainable speeds half those of salmon (0.36 m∙s−1). This confirms the low efficiency of jet-propelled swimming, and the resultant high cost of transport (12.5 J∙kg−1∙m−1; nearly 5 times that of salmon) raises interesting questions about how and why squid make large-scale vertical and horizontal migrations and the tactics they use to compete with fish that are both their predators and prey. Burst speeds after several maximal jets do not appear to be significantly greater than the peak speed after a single jet suggesting squid must depend primarily on maneuverability and high acceleration rather than high speed. A low capacity for accumulating an oxygen debt (73 mL O2∙kg−1) confirms predictions based on biochemical evidence. This debt is approximately equal to the energy needed to rephosphorylate muscle phosphagens.Key words: squid, swimming, oxygen consumption, oxygen debt, Loligo opalescens, metabolic rate, salmon, Oncorhynchus nerka

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