Effects of temperature on sustained swimming performance and swimming kinematics of the chub mackerelScomber japonicus

2002 ◽  
Vol 205 (7) ◽  
pp. 969-980 ◽  
Author(s):  
Kathryn A. Dickson ◽  
Jeanine M. Donley ◽  
Chugey Sepulveda ◽  
Lisa Bhoopat

SUMMARYThe effects of a 6°C difference in water temperature on maximum sustained swimming speed, swimming energetics and swimming kinematics were measured in the chub mackerel Scomber japonicus (Teleostei:Scombridae), a primarily coastal, pelagic predator that inhabits subtropical and temperate transition waters of the Atlantic, Pacific and Indian Oceans. New data for chub mackerel acclimated to 18°C are compared with published data from our laboratory at 24°C. Twelve individuals acclimated to each of two temperatures (15.6-26.3 cm fork length, FL, and 34-179g at 18°C; 14.0-24.7 cm FL and 26-156g at 24°C) swam at a range of speeds in a temperature-controlled Brett-type respirometer, at the respective acclimation temperature. At a given fish size, the maximum speed that S. japonicus was able to maintain for a 30-min period, while swimming steadily using slow, oxidative locomotor muscle (Umax,c),was significantly greater at 24 than at 18°C (52.5-97.5 cm s-1at 18°C and 70-120 cm s-1 at 24°C). At a given speed and fish size, the rate of oxygen consumption(V̇O2) was significantly higher at 24 than at 18°C because of a higher net cost of transport (1073-4617 J km-1 kg-1 at 18°C and 2708-14895 J km-1 kg-1 at 24°C). Standard metabolic rate, calculated by extrapolating the logV̇O2versus swimming speed relationship to zero speed, did not vary significantly with temperature or fish mass (126.4±67.2 mg O2 h-1 kg-1 at 18°C and 143.2±80.3 mg O2 h-1 kg-1 at 24°C; means ±S.D., N=12). Swimming kinematics was quantified from high-speed (120 Hz) video recordings analyzed with a computerized, two-dimensional motion-analysis system. At a given speed and fish size, there were no significant effects of temperature on tail-beat frequency, tail-beat amplitude or stride length, but propulsive wavelength increased significantly with temperature as a result of an increase in propulsive wave velocity. Thus, the main effects of temperature on chub mackerel swimming were increases in both Umax,c and the net cost of swimming at 24°C. Like other fishes, S. japonicus apparently must recruit more slow,oxidative muscle fibers to swim at a given sustainable speed at the lower temperature because of the reduced power output. Thus, the 24°C mackerel reach a higher speed before they must recruit the fast, glycolytic fibers,thereby increasing Umax,c at 24°C. By quantifying in vivo the effects of temperature on the swimming performance of an ectothermic species that is closely related to the endothermic tunas, this study also provides evidence that maintaining the temperature of the slow,oxidative locomotor muscle at 6°C or more above ambient water temperature in tunas should significantly increase sustainable swimming speeds, but also increase the energetic cost of swimming, unless cardiac output limits muscle performance.

1993 ◽  
Vol 178 (1) ◽  
pp. 97-108 ◽  
Author(s):  
P. W. Webb

Kinematics and steady swimming performance were recorded for steelhead trout (approximately 12.2 cm in total length) swimming in channels 4.5, 3 and 1.6 cm wide in the centre of a flume 15 cm wide. Channel walls were solid or porous. Tail-beat depth and the length of the propulsive wave were not affected by spacing of either solid or porous walls. The product of tail-beat frequency, F, and amplitude, H, was related to swimming speed, u, and to harmonic mean distance of the tail from the wall, z. For solid walls: FH = 1.01(+/−0.31)u0.67(+/−0.09)z(0.12+/−0.02) and for grid walls: FH = 0.873(+/−0.302)u0.74(+/−0.08)z0.064(+/−0.024), where +/−2 s.e. are shown for regression coefficients. Thus, rates of working were smaller for fish swimming between solid walls, but the reduction due to wall effects decreased with increasing swimming speed. Porous grid walls had less effect on kinematics, except at low swimming speeds. Spacing of solid walls did not affect maximum tail-beat frequency, but maximum tail-beat amplitude decreased with smaller wall widths. Maximum tail-beat amplitude similarly decreased with spacing between grid walls, but maximum tail-beat frequency increased. Walls also reduced maximum swimming speed. Wall effects have not been adequately taken into account in most studies of fish swimming in flumes and fish wheels.


2011 ◽  
Vol 8 (2) ◽  
pp. 266-269 ◽  
Author(s):  
Andrew M. Hein ◽  
Katrina J. Keirsted

Understanding the effects of water temperature on the swimming performance of fishes is central in understanding how fish species will respond to global climate change. Metabolic cost of transport (COT)—a measure of the energy required to swim a given distance—is a key performance parameter linked to many aspects of fish life history. We develop a quantitative model to predict the effect of water temperature on COT. The model facilitates comparisons among species that differ in body size by incorporating the body mass-dependence of COT. Data from 22 fish species support the temperature and mass dependencies of COT predicted by our model, and demonstrate that modest differences in water temperature can result in substantial differences in the energetic cost of swimming.


2021 ◽  
Author(s):  
Jacob. Fies ◽  
Brad J. Gemmell ◽  
Stephanie M. Fogerson ◽  
John H. Costello ◽  
Jennifer R. Morgan ◽  
...  

AbstractNeural and functional recovery in lampreys from spinal cord transection has been well documented. However, the extent of axon regeneration is highly variable and it is not known whether it is related to the level of behavioral recovery. To address this, we examined how swimming kinematics were related to axon regeneration by quantifying the relationship between swimming performance and percent axon regeneration of transected lampreys after 11 weeks of recovery. We found that swimming speed was not related to percent axon regeneration but it was closely related to body wave frequency and speed. However, wave frequency and speed varied greatly within individuals which resulted in swimming speed also varying within individuals. In fact, most recovered individuals, regardless of percent axon regeneration, could swim at fast and slow speeds. However, none of the transected individuals were able to generate body waves as large as the control lampreys. In order to swim faster, transected lampreys increased their wave frequencies and, as a result, transected lampreys had much higher frequencies than control lamprey at comparable swimming velocities. These data suggest that the control lampreys swam more efficiently than transected lampreys. In conclusion, there appears to be a minimal recovery threshold in terms of percent axon regeneration required for lampreys to be capable of swimming, however, there also seems to be a limit to how much they can behaviorally recover.


2000 ◽  
Vol 203 (20) ◽  
pp. 3089-3101 ◽  
Author(s):  
C. Sepulveda ◽  
K.A. Dickson

Tunas (Scombridae) have been assumed to be among the fastest and most efficient swimmers because they elevate the temperature of the slow-twitch, aerobic locomotor muscle above the ambient water temperature (endothermy) and because of their streamlined body shape and use of the thunniform locomotor mode. The purpose of this study was to test the hypothesis that juvenile tunas swim both faster and more efficiently than their ectothermic relatives. The maximum sustainable swimming speed (U(max), the maximum speed attained while using a steady, continuous gait powered by the aerobic myotomal muscle) and the net cost of transport (COT(net)) were compared at 24 degrees C in similar-sized (116–255 mm fork length) juvenile scombrids, an endothermic tuna, the kawakawa (Euthynnus affinis) and the ectothermic chub mackerel (Scomber japonicus). U(max) and COT(net) were measured by forcing individual fish to swim in a temperature-controlled, variable-speed swimming tunnel respirometer. There were no significant interspecific differences in the relationship between U(max) and body mass or fork length or in the relationship between COT(net) and body mass or fork length. Muscle temperatures were elevated by 1.0-2.3 degrees C and 0.1-0.6 degrees C above water temperature in the kawakawa and chub mackerel, respectively. The juvenile kawakawa had significantly higher standard metabolic rates than the chub mackerel, because the total rate of oxygen consumption at a given swimming speed was higher in the kawakawa when the effects of fish size were accounted for. Thus, juvenile kawakawa are not capable of higher sustainable swimming speeds and are not more efficient swimmers than juvenile chub mackerel.


1992 ◽  
Vol 70 (1) ◽  
pp. 94-98 ◽  
Author(s):  
Patrick J. Weatherhead ◽  
Ian C. Robertson

We examined the influence of body temperature on swimming speed of northern water snakes (Nerodia sipedon) and determined how variation in water temperature influenced their escape response. In a laboratory experiment, swimming speed increased as a function of water temperature and body size. Swimming speed was less thermally dependent at temperatures approximating the snakes' normal range of activity, suggesting that selection has favoured increased performance breadth at this range. In the field, basking snakes retreated to water when approached. Despite a decrease in swimming speed at lower temperatures, and the cost associated with reduced metabolic rate due to loss of body temperature, however, flight distances were independent of water temperature. We found that basking snakes retreated to water sooner when perched at lower heights, possibly indicating that N. sipedon are more vulnerable to predators when on low perches. Predicting water snake escape behaviour may require not only knowledge of variation both among snakes and in their environment, but also a better understanding of the interaction between the snakes and their natural predators.


Author(s):  
Beat Knechtle ◽  
Ram Barkai ◽  
Lee Hill ◽  
Pantelis T. Nikolaidis ◽  
Thomas Rosemann ◽  
...  

Ice swimming following the rules of IISA (International Ice Swimming Association) is a recent sports discipline starting in 2009. Since then, hundreds of athletes have completed an Ice Mile or an Ice Km in water colder than 5 °C. This study aimed to expand our knowledge about swimmers completing an Ice Mile or an Ice Km regarding the influence of anthropometric characteristics (i.e., body mass, body height, and body mass index, BMI) on performance. We analyzed data from 957 swimmers in the Ice Km (590 men and 367 women) and 585 swimmers in the Ice Mile (334 men and 251 women). No differences were found for anthropometric characteristics between swimmers completing an Ice Mile and an Ice Km although water temperatures and wind chill were lower in the Ice Km than in the Ice Mile. Men were faster than women in both the Ice Mile and Ice Km. Swimming speed decreased significantly with increasing age, body mass, and BMI in both women and men in both the Ice Mile and Ice Km. Body height was positively correlated to swimming speed in women in the Ice Km. Air temperature was significantly and negatively related to swimming speed in the Ice Km but not in the Ice Mile. Water temperature was not associated with swimming speed in men in both the Ice Mile and Ice Km but significantly and negatively in women in Ice Km. In summary, swimmers intending to complete an Ice Mile or an Ice Km do not need to have a high body mass and/or a high BMI to swim these distances fast.


Water ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1430
Author(s):  
Feifei He ◽  
Xiaogang Wang ◽  
Yun Li ◽  
Yiqun Hou ◽  
Qiubao Zou ◽  
...  

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.


2021 ◽  
Vol 8 ◽  
Author(s):  
Chenying Guo ◽  
Shin-ichi Ito ◽  
Michio Yoneda ◽  
Hajime Kitano ◽  
Hitoshi Kaneko ◽  
...  

Species-specific ecological traits in fishes are likely to vary between populations or stocks due to differences in regional oceanic conditions, such as latitudinal temperature. We examined potential intraspecific differences in the swimming performance and metabolism of Pacific chub mackerel (Scomber japonicus) from the Northwest and Northeast Pacific stocks, which are distributed on opposite sides of the North Pacific at similar latitudes, but where the temperature contrast is large. Swimming bioenergetics and metabolic data of Northwest stock mackerel were measured at 14, 18, and 24°C using variable-speed swim-tunnel respirometers, and then the resulting bioenergetic parameters were compared with previous findings from the Northeast stock. At a given size, the maximum sustainable swimming speed (Umax) of the Northwest stock showed no significant difference compared to the Northeast stock at 18 and 24°C, but was lower at 14°C. In addition, the oxygen consumption rate (MO2) of the Northwest stock showed lower mass dependence and different temperature dependence at a given swimming speed than in the Northeast stock. Combined with stock-specific data on growth and experienced temperatures in the wild, these bioenergetic differences indicate that the swimming performance and metabolism of the two stocks are specific to their local environment to maximize bioenergetic efficiency.


2015 ◽  
Vol 72 (8) ◽  
pp. 2506-2511 ◽  
Author(s):  
Cigdem Beyan ◽  
Bastian J. Boom ◽  
Jolanda M. P. Liefhebber ◽  
Kwang-Tsao Shao ◽  
Robert B. Fisher

Abstract Recent research on the relationship between coral reef water temperature and fish swimming activity has stated that swimming speed is inversely correlated with temperature above a species' optimum temperature (Johansen, J. L., and Jones, G. P. 2011. Increasing ocean temperature reduces the metabolic performance and swimming ability of coral reef damselfishes. Global Change Biology, 17: 2971–2979; Johansen, J. L., Messmer,V., Coker, D. J., Hoey, A. S., and Pratchett, M. S. 2014. Increasing ocean temperatures reduce activity patterns of a large commercially important coral reef fish. Global Change Biology, 20: 1067–1074). For tropical coral reefs, one anticipated consequence of global warming is an increase of ≥3°C in average water temperature in addition to greater thermal fluctuations [IPCC (Intergovernmental Panel on Climate Change). 2007. Summary for policymakers. In Climate Change 2007: The Physical Science Basis. Contribution of Working, Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Ed. by S. Solomon, D. Qin, and M. Manning et al. Cambridge University Press, Cambridge, UK; Lough, J. 2007. Climate and climate change on the Great Barrier Reef. In Climate Change and the Great Barrier Reef. Ed. by J. Johnson and P. A. Marshall, pp. 15–50. Great Barrier Reef Marine Park Authority and Australian Greenhouse Office, Townsville, Qld, Australia; Johansen and Jones, 2011]. Evaluating the behaviour of coral reef associated fish species at different temperatures can help to assess their sensitivity to climate change. In this study, the speed of freely swimming fish in a natural setting is investigated as a function of seasonal changes in water temperature, as contrasted with systematic temperature increases in a fish tank. We show that Dascyllus reticulatus swim faster as a function of increased water temperature over the range 20.9–30.3°C. The experiments were carried out using ∼3.6 million fish trajectories observed at the Kenting National Park in Taiwan. Fish speed was computed by detecting and tracking the fish through consecutive video frames, then converting image speeds to scene speeds. Temperatures were grouped into 10 intervals. The data reveal an ∼2 mm s−1 increase in average speed per additional temperature degree over the range of 20.9–30.3°C. The Mann–Kendall test using the mean and median speed for each interval revealed that there is a speed increase trend as temperature increases at the 0.05 significance level, rather than a random increase. Our results complement previous studies that investigated the effect of temperature on the swimming performance of different fish species in the laboratory (Johansen and Jones, 2011; Myrick, C. A. and Cech, J. J. 2000. Swimming performance of four California stream fishes: temperature effects. Environmental Biology of Fishes, 58: 289–295; Ojanguren, A. F. and Braña, F. 2000. Thermal dependence of swimming endurance in juvenile brown trout. Journal of Fish Biology, 56: 1342–1347; Lough 2007; Johansen et al., 2014).


2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Robert L Nudds ◽  
Karlina Ozolina ◽  
Miriam Fenkes ◽  
Oliver H Wearing ◽  
Holly A Shiels

Abstract Climate change is predicted to impact freshwater aquatic environments through changes to water temperature (Twater), river flow and eutrophication. Riverine habitats contain many economically and ecologically important fishes. One such group is the migratory salmonids, which are sensitive to warm Twater and low O2 (hypoxia). While several studies have investigated the independent effects of Twater and hypoxia on fish physiology, the combined effects of these stressors is less well known. Furthermore, no study has investigated the effects of Twater and O2 saturation levels within the range currently experienced by a salmonid species. Thus, the aim of this study was to investigate the simultaneous effects of Twater and O2 saturation level on the energetics and kinematics of steady-state swimming in brown trout, Salmo trutta. No effect of O2 saturation level (70 and 100% air saturation) on tail-beat kinematics was detected. Conversely, Twater (10, 14, 18 and 22°C) did affect tail-beat kinematics, but a trade-off between frequency (ftail) and amplitude (A, maximum tail excursion) maintained the Strouhal number (St = ftail• A/U, where U is swimming speed) within the theoretically most mechanically efficient range. Swimming oxygen consumption rate (${\dot{M}}_{{\mathsf{O}}_{\mathsf{2}}}$) and cost of transport increased with both U and Twater. The only effect of O2 saturation level was observed at the highest Twater (22°C) and fastest swimming speed (two speeds were used—0.6 and 0.8 m s−1). As the extremes of this study are consistent with current summer conditions in parts of UK waterways, our findings may indicate that S. trutta will be negatively impacted by the increased Twater and reduced O2 levels likely presented by anthropogenic climate change.


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