Impact of Diet on Metabolism and Swimming Performance in Juvenile Lake Trout, Salvelinus namaycush

1989 ◽  
Vol 46 (3) ◽  
pp. 384-388 ◽  
Author(s):  
F. W. H. Beamish ◽  
J. C. Howlett ◽  
T. E. Medland
Keyword(s):  
Oxygen Consumption ◽  
Swimming Speed ◽  
Lake Trout ◽  
Swimming Performance ◽  
Salvelinus Namaycush ◽  
Feeding Trial ◽  
Direct Association ◽  
Feeding Trials ◽  
Velocity Increments ◽  
Isocaloric Diets

Juvenile lake trout, Salvelinus namaycush, of similar size were fed one of three isocaloric diets, each differing in protein and lipid content. Oxygen consumption and swimming performance were measured in a recirculating water flume at intervals throughout the 70-d feeding trials (10 °C). Swimming speed was increased by stepwise velocity increments (5 cm∙s−1) and oxygen consumption was measured at each velocity between 20 and 45 cm∙s−1. Oxygen consumption for a given speed did not differ significantly throughout the feeding trial nor among the diets implying a similarity in the quality and quantity of substrate catabolized for energy. Basal metabolism (0 cm∙s−1) was also independent of diet and feeding interval. Critical swimming speed increased with dietary and carcass protein content to suggest a direct association with muscle mass and number of myofilaments.

The Swimming Energetics of Trout

1971 ◽  
Vol 55 (2) ◽  
pp. 521-540 ◽  
Author(s):  
P. W. WEBB
Keyword(s):  
Oxygen Consumption ◽  
Swimming Speed ◽  
Swimming Performance ◽  
The Body ◽  
Control Group ◽  
Muscle System ◽  
Rate Of Oxygen Consumption ◽  
Wet Weight ◽  
Standard Rate ◽  
The Difference

1. The oxygen consumption of rainbow trout was measured at a variety of subfatigue swimming speeds, at a temperature of 15 %C. Five groups of fish were used, a control group and four groups with extra drag loads attached to the body. 2. The logarithm of oxygen consumption was linearly related to swimming speed in all five groups, the slope of the relationship increasing with the size of the extra drag load. The mean standard rate of oxygen consumption was 72.5 mg O2/kg wet weight/h. The active rate of oxygen consumption was highest for the control group (628 mg O2/kg/h) and fell with increasing size of the attached drag load. The active rate for the control group was high in comparison with other salmonid fish, and in comparison with the value expected for the fish. This was not a result of the extra drag loads in the other groups. No explanation for this high value can be found. 3. The critical swimming speed for a 60 min test period was 58.1 cm/sec (2.0 body lengths/sec) for the control group. The values for the critical swimming speeds were slightly higher than those measured for the same species in a previous paper (Webb, 1971). The difference between the two sets of critical swimming speeds is attributed to seasonal changes in swimming performance. 4. The aerobic efficiency was found to reach values of 14.5-15.5% based on the energy released by aerobic metabolism in comparison with the calculated required thrust. 5. The anaerobic contribution to the total energy budget in increasing-velocity tests is considered to be small, and can be neglected. 6. It is concluded that the efficiency of the muscle system in cruising will be approximately 17-20% over the upper 80% of the cruising-speed range, while the caudal propeller efficiency will increase from about 15-75 % over the same range. 7. Consideration of the efficiency values for the caudal propeller calculated here, and those predicted by Lighthill's (1969) model of fish propulsion, suggest that the efficiency of the propeller system will reach an optimum value at the maximum cruising speeds of most fish, and will remain close to this value at spring speeds.

scholarly journals A tool for determining maximum sustained swimming ability of selected inland fish species in an Afrotropic ecozone

Water SA ◽  
2018 ◽  
Vol 44 (3 July) ◽  
Author(s):  
TL Botha ◽  
MP Mahloko ◽  
V Wepener ◽  
G Howatson ◽  
NJ Smit
Keyword(s):  
Oxygen Consumption ◽  
South African ◽  
Fish Species ◽  
Swimming Performance ◽  
Swimming Velocity ◽  
Flow Conditions ◽  
Physiological Strain ◽  
Volitional Exhaustion ◽  
Velocity Increments ◽  
Optimum Flow

Critical swimming speed (Ucrit) predicts the maximum sustained swimming velocity that various fish species are able to sustain for prolonged periods. The objective of this study was to determine the Ucrit of Afrotropic ecozone fish, determine oxygen consumption at Ucrit and relate the resulting optimum flow requirements to effective movement through fishways under South African flow conditions. The selected fish species were Coptodon rendalli, Tilapia sparrmanii, Pseudocrenilabrus philander, Oreochromis mossambicus and Enteromius trimaculatus. Ucrit and oxygen consumption (MO2) were measured in a swim respirometer at 5-min intervals, at increasing velocity increments of 0.5 cm·s−1 until volitional exhaustion. No significant differences were seen in the Ucrit values between C. rendalli, T. sparrmanii and P. philander, but all species significantly differed from O. mossambicus and E. trimaculatus, which had the highest Ucrit (17.6 ± 1.5 bl·s−1 and 18.2 ± 2.8 bl·s−1). Size plays an important role in the swimming performance of fish, with larger fish able to sustain a greater velocity, which was specifically true for O. mossambicus in this study. Additionally, smaller fish consumed more oxygen during swimming and therefore used more energy, experiencing relative physiological strain. Based on these data, flow respirometry was shown to be a useful tool to determining prolonged swimming abilities of South African fish species, and can help inform the structure and flow rates of culverts and fishways.

Effects of Low-Level Gas Supersaturation on Lake Trout (Salvelinus namaycush)

1988 ◽  
Vol 45 (4) ◽  
pp. 666-674 ◽  
Author(s):  
William F. Krise ◽  
James W. Meade
Keyword(s):  
Lake Trout ◽  
Condition Factor ◽  
Barometric Pressure ◽  
Salvelinus Namaycush ◽  
Feeding Trial ◽  
Frequency Distributions ◽  
Treatment Groups ◽  
Lower Treatment ◽  
Region Length ◽  
Average Condition

Eggs, eleutheroembryos, and alevins of lake trout (Salvelinus namaycush) were reared in 1 of 10 levels of total gas pressure (TCP) ranging from 13 to 81 mm Hg (ΔP) above ambient barometric pressure. Rearing water was soft (30–40 mg CaCO3/L, pH 6.8), temperature was 9.3 °C, and the exogenous feeding portion of the test lasted 98 d. The supersaturation levels tested had no effect on the total survival of eggs, eleutheroembryos, or alevins, and condition factor and mean weight of fish in each treatment were statistically unchanged at the end of the study. Most of the fish that died during the feeding trial were small, had a below-average condition factor, and showed petechial hemorrhaging in the abdominal region. Length frequency distributions differed significantly among treatment groups after 56 d of feeding and remained different through 98 d. There was no difference in weight gain, condition factor, food conversion, and mortality, indicating that these measures are not useful for predicting or monitoring effects within the range of gas levels tested. The estimated incipient lowest level of effect of gas supersaturation remains unclear. A conservative recommendation of maximum supersaturation levels for small lake trout would be in the lower treatment levels used in this study.

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.

scholarly journals A Method for Estimating the Velocity at Which Anaerobic Metabolism Begins in Swimming Fish

Water ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1430
Author(s):  
Feifei He ◽  
Xiaogang Wang ◽  
Yun Li ◽  
Yiqun Hou ◽  
Qiubao Zou ◽  
...  
Keyword(s):  
Oxygen Consumption ◽  
Swimming Speed ◽  
Crucian Carp ◽  
Anaerobic Metabolism ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Critical Swimming Speed ◽  
Swimming Efficiency ◽  
Rate Of Oxygen Consumption ◽  
Tail Beat

Anaerobic metabolism begins before fish reach their critical swimming speed. Anaerobic metabolism affects the swimming ability of fish, which is not conducive to their upward tracking. The initiation of anaerobic metabolism therefore provides a better predictor of flow barriers than critical swimming speed. To estimate the anaerobic element of metabolism for swimming fish, the respiratory metabolism and swimming performance of adult crucian carp (Carassius auratus, mass = 260.10 ± 7.93, body length = 19.32 ± 0.24) were tested in a closed tank at 20 ± 1 °C. The swimming behavior and rate of oxygen consumption of these carp were recorded at various swimming speeds. Results indicate (1) The critical swimming speed of the crucian carp was 0.85 ± 0.032 m/s (4.40 ± 0.16 BL/s). (2) When a power function was fitted to the data, oxygen consumption, as a function of swimming speed, was determined to be AMR = 131.24 + 461.26Us1.27 (R2 = 0.948, p < 0.001) and the power value (1.27) of Us indicated high swimming efficiency. (3) Increased swimming speed led to increases in the tail beat frequency. (4) Swimming costs were calculated via rate of oxygen consumption and hydrodynamic modeling. Then, the drag coefficient of the crucian carp during swimming was calibrated (0.126–0.140), and the velocity at which anaerobic metabolism was initiated was estimated (0.52 m/s), via the new method described herein. This study adds to our understanding of the metabolic patterns of fish at different swimming speeds.

Influence of Temperature and Salinity Acclimation on Temperature Preferenda of the Euryhaline Fish Tilapia nilotica

1970 ◽  
Vol 27 (7) ◽  
pp. 1209-1214 ◽  
Author(s):  
F. W. H. Beamish
Keyword(s):  
Oxygen Consumption ◽  
Swimming Speed ◽  
Swimming Performance ◽  
Vertical Gradient ◽  
Maximum Temperature ◽  
Acclimation Temperature ◽  
Final Temperature ◽  
Salinity Acclimation ◽  
Influence Of Temperature ◽  
Tilapia Nilotica

When Tilapia nilotica was acclimated to temperatures of 15–35 C and salinities of 0–30‰ in a vertical gradient tank, maximum temperature preferenda occurred at acclimation temperatures of 20 and 25 irrespective of salinity. Preferenda declined as acclimation temperature was increased above 25 C and, except at 0 and 7.5‰, declined as acclimation temperature was decreased below 20 C. The pattern of the relation between final temperature preferenda and salinity was similar to that reported between oxygen consumption for a given sustained swimming speed and salinity. The final preferendum was lowest at 15‰, close to the isosmotic salinity of T. nilotica, and highest at the extremes, 0 and 30‰. Final temperature preferenda are in general agreement with optimum temperatures reported for growth, reproduction, and swimming performance.

The Metabolic Cost of Swimming in Ducks

1970 ◽  
Vol 53 (3) ◽  
pp. 763-777 ◽  
Author(s):  
HENRY D. PRANGE ◽  
KNUT SCHMIDT-NIELSEN
Keyword(s):  
Oxygen Consumption ◽  
Swimming Speed ◽  
Swimming Performance ◽  
Water Channel ◽  
Minimum Cost ◽  
Metabolic Cost ◽  
Power Input ◽  
Cost Of Transport ◽  
Overall Efficiency ◽  
The Cost

1. The metabolic cost of swimming was studied in mallard ducks (Anas platyrhynchos) which had been trained to swim steadily in a variable-speed water channel. 2. At speeds of from 0.35 to 0.50 m/sec the oxygen consumption remained relatively constant at approximately 2.2 times the resting level. At speeds of 0.55 m/sec and higher the oxygen consumption increased rapidly and reached 4.1 times resting at the maximum sustainable speed of 0.70 m/sec. 3. The maximum sustainable swimming speed of the ducks coincided with the limit predicted from hydrodynamic considerations of the water resistance of a displacement-hulled ship of the same hull length as a duck (0.33 m). 4. The cost of transport (metabolic rate/speed) reached a minimum of 5.77 kcal/kg km at a swimming speed of 0.50 m/sec. Ducks swimming freely on a pond were observed to swim at the speed calculated in experimental trials to give minimum cost of transport. 5. Drag measurements made with model ducks indicated a maximum overall efficiency (power output/power input) for the swimming ducks of about 5%. Ships typically have maximum efficiencies of 20-30%. Because of the difficulty in delimiting the cost of swimming activity alone from the other bodily functions of the duck, overall efficiency may present an incorrect description of the swimming performance of the duck relative to that of a ship. An hydrodynamic parameter such as speed/length ratio [speed/(hull length)½] whereby a duck excels conventional ships may present a more appropriate comparison.

Evidence of successful river spawning by lake trout (Salvelinus namaycush) in the Lower Niagara River, Lake Ontario

2021 ◽  
Author(s):  
Alexander Gatch ◽  
Dimitry Gorsky ◽  
Zy Biesinger ◽  
Eric Bruestle ◽  
Kelley Lee ◽  
...  
Keyword(s):  
Lake Trout ◽  
Lake Ontario ◽  
Salvelinus Namaycush ◽  
Niagara River

An examination of the PCB: lipid relationship among individual fish

1997 ◽  
Vol 54 (5) ◽  
pp. 1031-1038
Author(s):  
C A Stow ◽  
L J Jackson ◽  
J F Amrhein
Keyword(s):  
Salmo Trutta ◽  
Lake Michigan ◽  
Oncorhynchus Tshawytscha ◽  
Lake Trout ◽  
Coho Salmon ◽  
Salvelinus Namaycush ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Strong Linear Correlation ◽  
Brown Trout Salmo Trutta ◽  
The Relationship

We examined data from 1984 to 1994 for five species of Lake Michigan salmonids to explore the relationship between total PCB concentration and percent lipid. When we compared mean species lipid and PCB values, we found a strong linear correlation. When we compared values among individuals, we found modest positive PCB:lipid associations in brown trout (Salmo trutta), chinook salmon (Oncorhynchus tshawytscha), coho salmon (Oncorhynchus kisutch), and rainbow trout (Oncorhynchus mykiss) collected during spawning, but positive associations were not apparent among nonspawning individuals. Lake trout (Salvelinus namaycush) exhibited no discernible PCB:lipid relationship. Our results are not incompatible with previous observations that contaminants are differentially partitioned into lipids within a fish, but these results do suggest that lipids are not a major factor influencing contaminant uptake.

Sign in / Sign up

Export Citation Format

Share Document