scholarly journals Active tail flexion in concert with passive hydrodynamic forces improves swimming speed and efficiency

2021 ◽  
Vol 932 ◽  
Author(s):  
Haotian Hang ◽  
Sina Heydari ◽  
John H. Costello ◽  
Eva Kanso
Keyword(s):  
Swimming Speed ◽  
Swimming Performance ◽  
Vortex Sheet ◽  
The Body ◽  
Fluid Structure Interactions ◽  
Kinematic Factor ◽  
Fluid Environment ◽  
Passive Flexion ◽  
Convergent Design ◽  
Universal Rule

Fish typically swim by periodic bending of their bodies. Bending seems to follow a universal rule; it occurs at about one-third from the posterior end of the fish body with a maximum bending angle of about $30^{\circ }$ . However, the hydrodynamic mechanisms that shaped this convergent design and its potential benefit to fish in terms of swimming speed and efficiency are not well understood. It is also unclear to what extent this bending is active or follows passively from the interaction of a flexible posterior with the fluid environment. Here, we use a self-propelled two-link model, with fluid–structure interactions described in the context of the vortex sheet method, to analyse the effects of both active and passive body bending on the swimming performance. We find that passive bending is more efficient but could reduce swimming speed compared with rigid flapping, but the addition of active bending could enhance both speed and efficiency. Importantly, we find that the phase difference between the posterior and anterior sections of the body is an important kinematic factor that influences performance, and that active antiphase flexion, consistent with the passive flexion phase, can simultaneously enhance speed and efficiency in a region of the design space that overlaps with biological observations. Our results are consistent with the hypothesis that fish that actively bend their bodies in a fashion that exploits passive hydrodynamics can at once improve speed and efficiency.

Topology Optimization of the Caudal Fin of the Three-Dimensional Self-Propelled Swimming Fish

2014 ◽  
Vol 6 (06) ◽  
pp. 732-763 ◽  
Author(s):  
Zhiqiang Xin ◽  
Chuijie Wu
Keyword(s):  
Topology Optimization ◽  
Swimming Speed ◽  
Moving Boundary ◽  
Swimming Performance ◽  
Three Dimensional ◽  
The Body ◽  
Caudal Fin ◽  
Swimming Efficiency ◽  
Vorticity Flux ◽  
3D Topology

AbstractBased on the boundary vorticity-flux theory, topology optimization of the caudal fin of the three-dimensional self-propelled swimming fish is investigated by combining unsteady computational fluid dynamics with moving boundary and topology optimization algorithms in this study. The objective functional of topology optimization is the function of swimming efficiency, swimming speed and motion direction control. The optimal caudal fin, whose topology is different from that of the natural fish caudal fin, make the 3D bionic fish achieve higher swimming efficiency, faster swimming speed and better maneuverability. The boundary vorticity-flux on the body surface of the 3D fish before and after optimization reveals the mechanism of high performance swimming of the topology optimization bionic fish. The comparative analysis between the swimming performance of the 3D topology optimization bionic fish and the 3D lunate tail bionic fish is also carried out, and the wake structures of two types of bionic fish show the physical nature that the swimming performance of the 3D topology optimization bionic fish is significantly better than the 3D lunate tail bionic fish.

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 Swimming Performance of Four Carps on the Yangtze River for Fish Passage Design

2021 ◽  
Vol 13 (3) ◽  
pp. 1575
Author(s):  
Junjun Tan ◽  
Hong Li ◽  
Wentao Guo ◽  
Honglin Tan ◽  
Senfan Ke ◽  
...  
Keyword(s):  
Body Length ◽  
Swimming Speed ◽  
Swimming Performance ◽  
Fish Habitat ◽  
Silver Carp ◽  
Fish Passage ◽  
The Body ◽  
Bighead Carp ◽  
Black Carp ◽  
Burst Swimming

Anthropogenic engineered structures alter the local ecological connectivity of river and survival habitat of native fishes. The swimming performance is critical for establishing fish passage or fish habitat. This study evaluated the swimming performance of four carps (black carp, grass carp, silver carp and bighead carp) with smaller body lengths (1.0–9.0 cm) in a swimming flume. The results showed that the critical and burst swimming speed (m/s) of the four carps increased with the increased body length, and the relative (critical and burst) swimming speed (the critical and burst swimming speed divided by the body length, BL/s) decreases with body length. The critical and burst swimming speed of each species at two individual length groups (1.0–5.0 cm, 5.1–9.0 cm) was significantly different (p < 0.05), and the water velocities in fish passage should be less than the fish burst swimming speed. The results further provided the swimming performance data of juvenile carps and provided technical reference for the construction of fish passage and the restoration of ecological habitat.

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.

scholarly journals Feeding strategy of mackerel in the Norwegian Sea relative to currents, temperature, and prey

2015 ◽  
Vol 73 (4) ◽  
pp. 1127-1137 ◽  
Author(s):  
Leif Nøttestad ◽  
Justine Diaz ◽  
Hector Penã ◽  
Henrik Søiland ◽  
Geir Huse ◽  
...  
Keyword(s):  
Swimming Speed ◽  
Swimming Performance ◽  
Feeding Strategy ◽  
Near Field ◽  
Norwegian Sea ◽  
Swimming Direction ◽  
Atlantic Mackerel ◽  
The North ◽  
Foraging Rate ◽  
Feeding Resources

Abstract High abundance of Northeast Atlantic mackerel (Scomber scombrus L.), combined with limited food resources, may now force mackerel to enter new and productive regions in the northern Norwegian Sea. However, it is not known how mackerel exploit the spatially varying feeding resources, and their vertical distribution and swimming behaviour are also largely unknown. During an ecosystem survey in the Norwegian Sea during the summer feeding season, swimming direction, and speed of mackerel schools were recorded with high-frequency omnidirectional sonar in four different regions relative to currents, ambient temperature, and zooplankton. A total of 251 schools were tracked, and fish and zooplankton were sampled with pelagic trawl and WP-2 plankton net. Except for the southwest region, swimming direction of the tracked schools coincided with the prevailing northerly Atlantic current direction in the Norwegian Sea. Swimming with the current saves energy, and the current also provides a directional cue towards the most productive areas in the northern Norwegian Sea. Average mean swimming speed in all regions combined was ∼3.8 body lengths s−1. However, fish did not swim in a straight course, but often changed direction, suggesting active feeding in the near field. Fish were largest and swimming speed lowest in the northwest region which had the highest plankton concentrations and lowest temperature. Mackerel swam close to the surface at a depth of 8–39 m, with all schools staying above the thermocline in waters of at least 6°C. In surface waters, mackerel encounter improved foraging rate and swimming performance. Going with the flow until temperature is too low, based on an expectation of increasing foraging rate towards the north while utilizing available prey under way, could be a simple and robust feeding strategy for mackerel in the Norwegian Sea.

THE EFFECT OF SOLID AND POROUS CHANNEL WALLS ON STEADY SWIMMING OF STEELHEAD TROUT ONCORHYNCHUS MYKISS

1993 ◽  
Vol 178 (1) ◽  
pp. 97-108 ◽  
Author(s):  
P. W. Webb
Keyword(s):  
Swimming Speed ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Regression Coefficients ◽  
Steelhead Trout ◽  
Wall Effects ◽  
Fish Swimming ◽  
Wide Channel ◽  
Solid Walls ◽  
Tail Beat

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.

scholarly journals The Maximal Lactate Steady State Workload Determines Individual Swimming Performance

2021 ◽  
Vol 12 ◽  
Author(s):  
Gernot O. Hering ◽  
Jens Stepan
Keyword(s):  
Steady State ◽  
Blood Lactate ◽  
Swimming Speed ◽  
Lactate Threshold ◽  
Swimming Performance ◽  
Endurance Capacity ◽  
Sudden Increase ◽  
Maximal Lactate Steady State ◽  
Custom Made ◽  
Major Interest

The lactate threshold (LT) and the strongly related maximal lactate steady state workload (MLSSW) are critical for physical endurance capacity and therefore of major interest in numerous sports. However, their relevance to individual swimming performance is not well understood. We used a custom-made visual light pacer for real-time speed modulation during front crawl to determine the LT and MLSSW in a single-exercise test. When approaching the LT, we found that minute variations in swimming speed had considerable effects on blood lactate concentration ([La−]). The LT was characterized by a sudden increase in [La−], while the MLSSW occurred after a subsequent workload reduction, as indicated by a rapid cessation of blood lactate accumulation. Determination of the MLSSW by this so-called “individual lactate threshold” (ILT)-test was highly reproducible and valid in a constant speed test. Mean swimming speed in 800 and 1,500 m competition (S-Comp) was 3.4% above MLSSW level and S-Comp, and the difference between S-Comp and the MLSSW (Δ S-Comp/MLSSW) were higher for long-distance swimmers (800–1,500 m) than for short- and middle-distance swimmers (50–400 m). Moreover, Δ S-Comp/MLSSW varied significantly between subjects and had a strong influence on overall swimming performance. Our results demonstrate that the MLSSW determines individual swimming performance, reflects endurance capacity in the sub- to supra-threshold range, and is therefore appropriate to adjust training intensity in moderate to severe domains of exercise.

Pectoral fin locomotion in the striped surfperch. I. Kinematic effects of swimming speed and body size

1996 ◽  
Vol 199 (10) ◽  
pp. 2235-2242 ◽  
Author(s):  
E Drucker ◽  
J Jensen
Keyword(s):  
Body Size ◽  
Swimming Speed ◽  
Beat Frequency ◽  
Limited Range ◽  
The Body ◽  
Small Fish ◽  
Large Fish ◽  
Pectoral Fin ◽  
Transition Speed ◽  
Speed Up

Swimming trials at increasing velocity were used to determine the effects of steady swimming speed on pectoral fin kinematics for an ontogenetic series of striped surfperch Embiotoca lateralis, ranging from 6 to 23 cm in standard length (SL). The fin stroke cycle consisted of a propulsive period, the duration of fin abduction and adduction, and a 'refractory' period, during which the fin remained adducted against the body. Pectoral fin-beat frequency (fp) measured as the inverse of the entire stride period, as in past studies, increased curvilinearly with speed. Frequency, calculated as the reciprocal of the propulsive period alone, increased linearly with speed, as shown previously for tail-beat frequency of fishes employing axial undulation. Fin-beat amplitude, measured as the vertical excursion of the pectoral fin tip during abduction, increased over a limited range of low speeds before reaching a plateau at 0.35&shy;0.40 SL. Pectoral fin locomotion was supplemented by intermittent caudal fin undulation as swimming speed increased. At the pectoral&shy;caudal gait transition speed (Up-c), frequency and amplitude attained maxima, suggesting that the fin musculature reached a physiological limit. The effects of body size on swimming kinematics differed according to the method used for expressing speed. At a given absolute speed, small fish used higher stride frequencies and increased frequency at a faster rate than large fish. In contrast, the relationship between fp and length-specific speed (SL s-1) had a greater slope for large fish and crossed that for small fish at high speeds. We recommend that comparisons across size be made using speeds expressed as a percentage of Up-c, at which kinematic variables influencing thrust are size-independent.

Kinematics and efficiency of steady swimming in adult axolotls (Ambystoma mexicanum)

1997 ◽  
Vol 200 (13) ◽  
pp. 1863-1871 ◽  
Author(s):  
K D'Août ◽  
P Aerts
Keyword(s):  
Swimming Speed ◽  
High Speed ◽  
Natural Habitat ◽  
Total Body Length ◽  
Ambystoma Mexicanum ◽  
The Body ◽  
Entire Body ◽  
Amplitude Profile ◽  
Wide Range ◽  
Tail Tip

The kinematics of steady swimming at a wide range of velocities was analysed using high-speed video recordings (500 frames s-1) of eight individuals of Ambystoma mexicanum swimming through a tunnel containing stationary water. Animals in the observed size range (0.135&shy;0.238 m total body length) prefer to swim at similar absolute speeds, irrespective of their body size. The swimming mechanism is of the anguilliform type. The measured kinematic variables &shy; the speed, length, frequency and amplitude (along the entire body) of the propulsive wave &shy; are more similar to those of anguilliform swimming fish than to those of tadpoles, in spite of common morphological features with the latter, such as limbs, external gills and a tapering tail. The swimming speed for a given animal size correlates linearly with the tailbeat frequency (r2=0.71), whereas the wavelength and tail-tip amplitude do not correlate with this variable. The shape of the amplitude profile along the body, however, is very variable between the different swimming bouts, even at similar speeds. It is suggested that, for a given frequency, the amplitude profile along the body is adjusted in a variable way to yield the resulting swimming speed rather than maintaining a fixed-amplitude profile. The swimming efficiency was estimated by calculating two kinematic variables (the stride length and the propeller efficiency) and by applying two hydrodynamic theories, the elongated-body theory and an extension of this theory accounting for the slope at the tail tip. The latter theory was found to be the most appropriate for the axolotl's swimming mode and yields a hydromechanical efficiency of 0.75&plusmn;0.04 (mean &plusmn; s.d.), indicating that Ambystoma mexicanum swims less efficiently than do anuran tadpoles and most fishes. This can be understood given its natural habitat in vegetation at the bottom of lakes, which would favour manoeuvrability and fast escape.

Effect of Morphological Fin-Curl on the Swimming Performance and Station-Holding Ability of Juvenile Shovelnose Sturgeon

2016 ◽  
Vol 7 (1) ◽  
pp. 198-204 ◽  
Author(s):  
David Deslauriers ◽  
Ryan Johnston ◽  
Steven R. Chipps
Keyword(s):  
Swimming Speed ◽  
Early Onset ◽  
Positive Relationship ◽  
Swimming Performance ◽  
Fork Length ◽  
Critical Swimming Speed ◽  
Pectoral Fin ◽  
Speed Test ◽  
Shovelnose Sturgeon ◽  
Pectoral Fins

Abstract We assessed the effect of fin-curl on the swimming and station-holding ability of juvenile shovelnose sturgeon Scaphirhynchus platorynchus (mean fork length = 17 cm; mean weight = 16 g; n = 21) using a critical swimming speed test performed in a small swim chamber (90 L) at 20°C. We quantified fin-curl severity using the pectoral fin index. Results showed a positive relationship between pectoral fin index and critical swimming speed indicative of reduced swimming performance displayed by fish afflicted with a pectoral fin index &lt; 8%. Fin-curl severity, however, did not affect the station-holding ability of individual fish. Rather, fish affected with severe fin-curl were likely unable to use their pectoral fins to position their body adequately in the water column, which led to the early onset of fatigue. Results generated from this study should serve as an important consideration for future stocking practices.

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