scholarly journals The influence of cerebellar lesions on the swimming performance of the trout

1992 ◽  
Vol 167 (1) ◽  
pp. 171-178
Author(s):  
B. L. Roberts ◽  
A. van Rossem ◽  
S. de Jager
Keyword(s):  
Swimming Performance ◽  
Beat Frequency ◽  
Water Tunnel ◽  
Histological Investigation ◽  
Post Mortem ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Cerebellar Lesions ◽  
All Speeds ◽  
The Relationship ◽  
Tail Beat

The influence of partial cerebellar ablation on the performance of rainbow trout, Oncorhynchus mykiss, swimming in a water tunnel was studied. Before surgery, all fish maintained a steady position in the water tunnel at all speeds tested. A linear relationship was found between the specific velocity (body length s-1) and the tail-beat frequency. After partial cerebellectomy, the fish swam well in the tunnel at low speeds, retaining the relationship between tail-beat frequency and specific velocity, but they were unable to maintain a steady position at water speeds requiring tail-beat frequencies above 3.5 s-1 and were swept backwards. Two sham-operated fish swam at all water speeds tested. Post mortem histological investigation showed that the lesions were restricted to the cerebellar corpus. We conclude that the cerebellum plays no role in the generation of motor programmes but may be essential for their selection and implementation.

Swimming performance and behaviour of young-of-the-year shortnose sturgeon (Acipenser brevirostrum) under fixed and increased velocity swimming tests

2012 ◽  
Vol 90 (3) ◽  
pp. 345-351 ◽  
Author(s):  
D. Deslauriers ◽  
J.D. Kieffer
Keyword(s):  
Swimming Performance ◽  
Beat Frequency ◽  
Significant Negative Correlation ◽  
Shortnose Sturgeon ◽  
Fish Swimming ◽  
Acipenser Brevirostrum ◽  
Burst Swimming ◽  
Young Of The Year ◽  
All Speeds ◽  
Tail Beat

Swimming performance and behaviour in fish has been shown to vary depending on the investigation method. In this study, an endurance swimming curve was generated for young-of-the-year shortnose sturgeon (Acipenser brevirostrum LeSueur, 1818) (~7 cm total length, ~2 g) and compared with values determined in a separate incremental swimming (critical swimming, Ucrit) test. Using video, tail-beat frequency (TBF) was quantified and compared for fish swimming under both swimming tests. From the endurance-curve analysis, it was found that sturgeon did not display a statistically significant burst swimming phase. Maximum sustainable swimming speed (calculated to be 18.00 cm·s–1) from the endurance curve occurred at ~80% of Ucrit (22.30 cm·s–1). TBF was similar at all speeds for both swimming tests, except at speeds approaching Ucrit, where fish displayed TBFs of 4.29 Hz for the endurance protocol and 2.26 Hz for the Ucrit protocol. TBF was more variable between individuals swimming at the same speed within the Ucrit compared with the endurance protocol. Finally, a significant negative correlation was found between TBF and Ucrit in individual fish, suggesting that station-holding may be an important energy saving strategy during swimming in this size class of sturgeon.

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 Fish and Robots Swimming Together in a Water Tunnel: Robot Color and Tail-Beat Frequency Influence Fish Behavior

PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e77589 ◽  
Author(s):  
Giovanni Polverino ◽  
Paul Phamduy ◽  
Maurizio Porfiri
Keyword(s):  
Beat Frequency ◽  
Fish Behavior ◽  
Water Tunnel ◽  
Tail Beat

STUDIES OF TROPICAL TUNA SWIMMING PERFORMANCE IN A LARGE WATER TUNNEL - KINEMATICS

1994 ◽  
Vol 192 (1) ◽  
pp. 45-59 ◽  
Author(s):  
H Dewar ◽  
J Graham
Keyword(s):  
Swimming Performance ◽  
Beat Frequency ◽  
Fork Length ◽  
Swimming Velocity ◽  
Water Tunnel ◽  
Pectoral Fins ◽  
Swimming Mode ◽  
Anatomical Adaptations ◽  
Large Water ◽  
Tropical Tuna

Yellowfin tuna (Thunnus albacares) swimming kinematics was studied in a large water tunnel at controlled swimming velocities (U). Quantified kinematic variables included the tail-beat frequency, stride length (l), caudal amplitude, yaw, the propulsive wavelength, the speed of the propulsive wave (C) and the sweepback angle of the pectoral fins. In general, all variables, except the propulsive wavelength and consequently C, are comparable to values determined for other teleosts. The propulsive wavelength for the tunas (1.23­1.29 L, where L is fork length) is 30­60 % longer than in other cruise-adapted teleosts such as salmonids. The resulting thunniform swimming mode and the morphological and anatomical adaptations associated with the long propulsive wavelength (e.g. fusiform body shape, rigid vertebral column) act to minimize anterior resistance and maximize caudal thrust. The long propulsive wavelength also increases the maximum l which, in concert with the elevated muscle temperatures of tunas, increases their maximum swimming velocity.

On the Function of the White Muscles in Teleosts at Intermediate Swimming Speeds

1973 ◽  
Vol 58 (2) ◽  
pp. 509-522 ◽  
Author(s):  
RICHARD C. L. HUDSON
Keyword(s):  
Rainbow Trout ◽  
Linear Relationship ◽  
Muscle Mass ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Salmo Gairdneri ◽  
Electrical Activities ◽  
Tail Beat ◽  
Increased Activity

1. The swimming performance of rainbow trout, Salmo gairdneri, and the electrical activities, recorded extracellularly, of its red and mosaic muscles have been studied at different swimming speeds. 2. A linear relationship was found between the specific velocity (body lengths/sec) and the frequency of tail beating at frequencies up to 5/sec. 3. The red muscles are active at all swimming speeds at which the fish swim by tail oscillations. Discharges from this muscle decrease in duration with frequency up to 3.5-5.0 beats/sec and then increase while the interburst interval decreases linearly with tail-beat frequency. 4. Mosaic muscle becomes active at 3.05-3.60 tail beats/sec and increases slightly with increasing frequency of tail oscillations. Greatly increased activity was recorded in response to struggling and rapid accelerations. 5. The white (mosaic) muscle mass of teleosts is concluded to be involved at intermediate swimming speeds and to be active at the higher range of cruising speeds.

Going against the flow: an examination of the propulsive movements made by young brook trout in streams

1998 ◽  
Vol 55 (4) ◽  
pp. 853-860 ◽  
Author(s):  
Robert L McLaughlin ◽  
David LG Noakes
Keyword(s):  
Brook Trout ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Fork Length ◽  
Spatial Location ◽  
Laboratory Studies ◽  
Pectoral Fins ◽  
Tail Beat ◽  
Temporal And Spatial Heterogeneity ◽  
A Current

We examined the propulsive movements and behaviour of young-of-the-year (YOY) brook trout (Salvelinus fontinalis) swimming in their natal streams. Our findings demonstrated that swimming performance was influenced by temporal and spatial heterogeneity in water flow. Pectoral fins were used commonly, even by individuals swimming in fast flowing water. There also was spatial variation in the speed attained for a given tail-beat frequency and amplitude. After controlling statistically for variation in spatial location, fork length, and tail-beat amplitude, the swimming speeds brook trout attained for a given tail-beat frequency were lower than values expected from laboratory studies of steady swimming but higher than values expected from laboratory studies of unsteady swimming in standing water. Trout holding station made short-term adjustments in tail-beat frequency also suggesting a degree of unsteady swimming. A field experiment demonstrated that introduction of a current-velocity refuge reduced swimming costs by 10%, on average, without affecting the frequency of foraging attempts made.

Aspects of Shark Swimming Performance Determined Using a Large Water Tunnel

1990 ◽  
Vol 151 (1) ◽  
pp. 175-192 ◽  
Author(s):  
JEFFREY B. GRAHAM ◽  
HEIDI DEWAR ◽  
N. C. LAI ◽  
WILLIAM R. LOWELL ◽  
STEVE M. ARCE
Keyword(s):  
Body Size ◽  
Swimming Speed ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Swimming Velocity ◽  
Water Tunnel ◽  
Lemon Shark ◽  
Negaprion Brevirostris ◽  
Leopard Shark ◽  
Triakis Semifasciata

A large, sea-going water tunnel was used in various studies of shark swimming performance. The critical swimming velocity (Ucrit, an index of aerobically sustainable swimming speed) of a 70 cm long lemon shark (Negaprion brevirostris Poey) was determined to be 1.1 Ls−1, where L is body length. The Ucrit of the leopard shark (Triakis semifasciata Girard) was found to vary inversely with body size; from about 1.6Ls−1in 30–50cm sharks to 0.6LS−1 in 120cm sharks. Large Triakis adopt ram gill ventilation at swimming speeds between 27 and 60cms−1, which is similar to the speed at which this transition occurs in teleosts. Analyses of tail-beat frequency (TBF) in relation to velocity and body size show that smaller Triakis have a higher TBF and can swim at higher relative speeds. TBF, however, approaches a maximal value at speeds approaching Ucrit, suggesting that red muscle contraction velocity may limit sustained swimming speed. The TBF of both Triakis and Negaprion rises at a faster rate with swimming velocity than does that of the more thunniform mako shark (Isurus oxyrinchus Rafinesque). This is consistent with the expectation that, at comparable relative speeds, sharks adapted for efficient swimming should have a lower TBF. The rates of O2 consumption of swimming lemon and mako sharks are among the highest yet measured for elasmobranchs and are comparable to those of cruise-adapted teleosts.

Tuna robotics: A high-frequency experimental platform exploring the performance space of swimming fishes

2019 ◽  
Vol 4 (34) ◽  
pp. eaax4615 ◽  
Author(s):  
J. Zhu ◽  
C. White ◽  
D. K. Wainwright ◽  
V. Di Santo ◽  
G. V. Lauder ◽  
...  
Keyword(s):  
High Frequency ◽  
High Performance ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Cost Of Transport ◽  
Low Frequencies ◽  
Atlantic Mackerel ◽  
Performance Space ◽  
Wide Range ◽  
Tail Beat

Tuna and related scombrid fishes are high-performance swimmers that often operate at high frequencies, especially during behaviors such as escaping from predators or catching prey. This contrasts with most fish-like robotic systems that typically operate at low frequencies (< 2 hertz). To explore the high-frequency fish swimming performance space, we designed and tested a new platform based on yellowfin tuna (Thunnus albacares) and Atlantic mackerel (Scomber scombrus). Body kinematics, speed, and power were measured at increasing tail beat frequencies to quantify swimming performance and to study flow fields generated by the tail. Experimental analyses of freely swimming tuna and mackerel allow comparison with the tuna-like robotic system. The Tunabot (255 millimeters long) can achieve a maximum tail beat frequency of 15 hertz, which corresponds to a swimming speed of 4.0 body lengths per second. Comparison of midline kinematics between scombrid fish and the Tunabot shows good agreement over a wide range of frequencies, with the biggest discrepancy occurring at the caudal fin, primarily due to the rigid propulsor used in the robotic model. As frequency increases, cost of transport (COT) follows a fish-like U-shaped response with a minimum at ~1.6 body lengths per second. The Tunabot has a range of ~9.1 kilometers if it swims at 0.4 meter per second or ~4.2 kilometers at 1.0 meter per second, assuming a 10–watt-hour battery pack. These results highlight the capabilities of high-frequency biological swimming and lay the foundation to explore a fish-like performance space for bio-inspired underwater vehicles.

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.

scholarly journals Effect of tail fin loss on swimming capability and tail beat frequency of juvenile black carp Mylopharyngodon piceus

2020 ◽  
Vol 29 ◽  
pp. 71-77
Author(s):  
L Cai ◽  
J Chen ◽  
D Johnson ◽  
Z Tu ◽  
Y Huang
Keyword(s):  
Swimming Speed ◽  
Beat Frequency ◽  
Fish Swimming ◽  
Black Carp ◽  
No Tail ◽  
In The Wild ◽  
Group A ◽  
Mylopharyngodon Piceus ◽  
The Relationship ◽  
Tail Beat

Fin clipping is a common practice in fisheries management, and hatchery fish are often marked this way. In the wild, the tail (caudal) fin may be damaged or lost to predation or disease. Because the tail fin is important to fish swimming behavior and ability, this study was designed to examine the effects of partial and complete loss of the tail fin on the swimming ability of juvenile black carp Mylopharyngodon piceus. Swimming speed and tail beat frequency were measured for 3 groups (intact tail fin, partial tail fin, no tail fin) using a stepped velocity test conducted in a fish respirometer. We found that critical swimming speed (Ucrit) and burst speed (Uburst) decreased slightly in the partial fin group and significantly in the no fin group. In the group with no tail fin, Uburst decreased more than Ucrit, clearly reducing the ability to avoid predators. Moreover, mean tail beat frequency (TBFmean), Ucrit and Uburst all decreased slightly in the partial fin group and significantly in the no fin group. A decrease in tail beat force and TBF both reduce swimming capability. These findings contribute to developing our understanding of the relationship between fish tail fins and swimming.

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