The effect of temperature on tail beat frequency of fish swimming at constant velocity

1979 ◽  
Vol 57 (8) ◽  
pp. 1628-1635 ◽  
Author(s):  
E. Don Stevens
Keyword(s):  
Test Temperature ◽  
Beat Frequency ◽  
Velocity Curve ◽  
Effect Of Temperature ◽  
Acclimation Temperature ◽  
Fish Swimming ◽  
Force Velocity ◽  
Higher Temperature ◽  
Three Body ◽  
Tail Beat

Rainbow trout and largemouth bass were swum at fixed swim speeds from one to three body lengths per second at ambient water temperatures from 5 to 35 °C. Tail beat frequency was measured during steady swimming. Both tail beat frequency and stride length (distance moved per tail beat) increased with increased swim speed. In trout tail beat frequency was lower at higher water temperatures, whereas in bass tail beat frequency was higher at higher water temperatures. In both trout and bass tail beat frequency was lower in fish acclimated to a higher temperature. I suggest that when test temperature is above acclimation temperature the muscle operates high on the force–velocity curve; and when test temperature is below acclimation temperature the muscle operates low on the force–velocity curve.

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.

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.

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.

The Effect of Temperature on the Burst Swimming Performance of Fish Larvae

1992 ◽  
Vol 170 (1) ◽  
pp. 187-201 ◽  
Author(s):  
R. S. BATTY ◽  
J. H. S. BLAXTER
Keyword(s):  
High Speed ◽  
Stride Length ◽  
Fish Larvae ◽  
Swimming Performance ◽  
Beat Frequency ◽  
Effect Of Temperature ◽  
Temperature Dependent ◽  
Burst Swimming ◽  
Tail Beat ◽  
Escape Speed

Newly hatched herring and plaice larvae were stimulated by probes to make C-start escape responses at temperatures between 5 and 15 °C. The responses and the subsequent burst-speed swimming were recorded and analysed using high-speed video at 400 frames s−1. The muscle contraction time of the initial C-start was temperature-dependent, ranging from 22–33 ms at 5°C to 17–21 ms at 15°C. Immediately following the C-start, tail-beat frequency ranged from 18s−1 at 5°C to 35 s−1 at 15°C. Tail-beat amplitude, equivalent to 0.4-0.6 of a body length (L), and stride length, about 0.5 L, were not temperature-dependent. The escape speed ranged from 8 Ls−1 at 5°C to 15 Ls−1 at 15 °C. These results and those of other workers can be described by the equation: f=100e−99/(t+29.5)L−0.266, where f is tail-beat frequency, t is temperature and L is length.

Nucleation of Disorder in Fe3Al Alloys

1967 ◽  
Vol 25 ◽  
pp. 312-313
Author(s):  
P. R. Swann ◽  
W. R. Duff ◽  
R. M. Fisher
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Annealing Temperature ◽  
Antiphase Domain ◽  
Effect Of Temperature ◽  
Domain Structures ◽  
Transmission Electron ◽  
Domain Boundaries ◽  
Higher Temperature ◽  
The One

Recently we have investigated the phase equilibria and antiphase domain structures of Fe-Al alloys containing from 18 to 50 at.% Al by transmission electron microscopy and Mössbauer techniques. This study has revealed that none of the published phase diagrams are correct, although the one proposed by Rimlinger agrees most closely with our results to be published separately. In this paper observations by transmission electron microscopy relating to the nucleation of disorder in Fe-24% Al will be described. Figure 1 shows the structure after heating this alloy to 776.6°C and quenching. The white areas are B2 micro-domains corresponding to regions of disorder which form at the annealing temperature and re-order during the quench. By examining specimens heated in a temperature gradient of 2°C/cm it is possible to determine the effect of temperature on the disordering reaction very precisely. It was found that disorder begins at existing antiphase domain boundaries but that at a slightly higher temperature (1°C) it also occurs by homogeneous nucleation within the domains. A small (∼ .01°C) further increase in temperature caused these micro-domains to completely fill the specimen.

Effect of Temperature on Column Bioleaching of a Refractory Gold Ore

2013 ◽  
Vol 825 ◽  
pp. 352-355 ◽  
Author(s):  
Zeng Ling Wu ◽  
Zhong Sheng Huang ◽  
Ren Man Ruan ◽  
Shui Ping Zhong ◽  
Brenda K.C. Chan
Keyword(s):  
Sulfide Oxidation ◽  
Effect Of Temperature ◽  
Low Grade ◽  
Key Factors ◽  
Gold Extraction ◽  
Gold Ores ◽  
Fraction Distribution ◽  
Higher Temperature ◽  
Liberation Analysis ◽  
Main Factor

Low-grade, finely disseminated refractory sulfide gold ores associated with high arsenic are ubiquitous resources all over the world. Since heap bio-oxidation is an economic and promising biotechnology to recover gold, low grade, high organic carbon and arsenic bearing gold ores from Zhesang Mines in China were chosen for this purpose to study the key factors that would affect biooxidation. Pyrite and arsenopyrite (particle size 0.002-0.22 mm) were the main minerals from Mineral Liberation Analysis (MLA). Column biooxidation and cyanidation of mineral size < 10 mm were evaluated for its potential for gold extraction. Results showed that temperature was the main factor influencing sulfide oxidation. 58-67 % of sulfide was oxidized at 35-45°C after > 240 days of biooxidation with mixed mesophiles, while higher sulfide-S dissolution (77%) was obtained at 60°C. Sulfide-S fraction distribution revealed higher mineral decomposition, finer fractions and eventually higher sulfide oxidation at 60°C. Jarosite and scorodite were found from the residues at 60°C by SEM and EDX, which implies higher temperature accelerated arsenic precipitation. No elemental sulfur was detected during the biooxidation at 35-60°C. After bio-oxidation, column cyanidation was successfully demonstrated recovery of gold from the residues, with gold extraction rate reaching 66%.

The Kinematics of Swimming in Larvae of the Clawed Frog, Xenopus Laevis

1986 ◽  
Vol 122 (1) ◽  
pp. 1-12 ◽  
Author(s):  
KARIN VON SECKENDORFF HOFF ◽  
RICHARD JOEL WASSERSUG
Keyword(s):  
Xenopus Laevis ◽  
Swimming Speed ◽  
High Speed ◽  
Total Mass ◽  
Beat Frequency ◽  
Maximum Amplitude ◽  
Open Water ◽  
Computer Assisted ◽  
Anuran Larvae ◽  
Tail Beat

The kinematics of swimming in larval Xenopus laevis has been studied using computer-assisted analysis of high-speed (200 frames s−1) ciné records. The major findings are as follows. 1. At speeds below 6 body lengths (L) per second, tail beat frequency is approximately 10 Hz and, unlike for most aquatic vertebrates, is not correlated with specific swimming speed. At higher speeds, tail beat frequency and speed are positively correlated. 2. Xenopus tadpoles show an increase in the maximum amplitude of the tail beat with increasing velocity up to approximately 6Ls−1. Above that speed amplitude approaches an asymptote at 20 % of body length. 3. Anterior yaw is absent at velocities below 6Ls−1, unlike for other anuran larvae, but is present at higher speeds. 4. At speeds below 6Ls−1 there is a positive linear relationship between length of the propulsive wave (λ) and specific swimming speed. At higher speeds wavelength is constant at approximately 0.8L. 5. There is a shift in the modulation of wavelength and tail beat frequency with swimming speed around 5.6Ls−1, suggesting two different swimming modes. The slower mode is used during open water cruising and suspension feeding. The faster, sprinting mode may be used to avoid predators. 6. Froude efficiencies are similar to those reported for fishes and other anuran larvae. 7. Unlike Rana and Bufo larvae, the axial muscle mass of Xenopus increases dramatically with size from less than 10% of total mass for the smallest animals to more than 45% of total mass for the largest animals. This increase is consistent with maintaining high locomotor performance throughout development.

The Mechanical Characteristics and Sealing Performance Evaluation of Bolted Pipe Flange Connections With Metallic Flat Gaskets Subjected to Internal Pressure

2016 ◽  
Author(s):  
Koji Kondo ◽  
Koji Sato ◽  
Satomi Takahashi ◽  
Toshiyuki Sawa
Keyword(s):  
Plastic Deformation ◽  
Mechanical Characteristics ◽  
Experimental Results ◽  
Leak Rate ◽  
Effect Of Temperature ◽  
Load Factor ◽  
Stress Distributions ◽  
Bolt Preload ◽  
Sealing Performance ◽  
Higher Temperature

Bolted pipe flange connections with metallic gaskets have been used under higher pressure as well as higher temperature. However, a few researches on the mechanical characteristics in connections with metallic gaskets have been carried out. It is necessary to examine the mechanical characteristics such as the contact gasket stress distributions which govern the sealing performance, the deformation of the metallic gaskets, changes in axial bolt forces and the hub stress under higher pressure and temperature. In the present paper, the objectives are to examine the changes in axial bolt forces, the hub stress and the contact gasket stress distributions and the sealing performance of the pipe flange connections with metallic flat gaskets. Firstly, the mechanical characteristics of the connections under higher pressure are analyzed using FEA. Then, experiments were carried out to measure the load factor, the hub stress and the leak rate (the sealing performance). The relationship between the average contact gasket stress and the leak rate was measured using platen device at room temperature. The FEA results are fairly coincided with the experimental results. It is shown that the leak rate decreases as the contact gasket stress increases and when the plastic deformation of gaskets occurs, the sealing performance increases. The leak rate was measured in the range of 10−4∼10−7 [Pa·m3/s]. It is found that the sealing performance increases as the gasket width increase in the elastic deformation range while it is independent of the gasket width when the plastic deformation occurs. The effect of temperature on the mechanical characteristics of the connection is also examined. The FEA results are in a fairly good agreement with the experimental results. It is found that the sealing performance increases as the temperature increases. In addition, a method how to determine the bolt preload for increasing the sealing performance is proposed.

scholarly journals Effect of High Temperature on the Electrochemical and Optical Properties of Emeraldine Salt Doped with DBSA and Sulfuric Acid

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Salma Gul ◽  
Anwar-ul-Haq Ali Shah ◽  
Salma Bilal
Keyword(s):  
Thermal Stability ◽  
Cyclic Voltammetry ◽  
Sulfuric Acid ◽  
Effect Of Temperature ◽  
Visible Spectroscopy ◽  
Emeraldine Salt ◽  
Higher Temperature ◽  
Stability Effect ◽  
Thermal Stability Of ◽  
Comprehensive Study

A comprehensive study of thermally treated polyaniline in its emeraldine salt form is presented here. It offers an understanding of the thermal stability of the polymer. Emeraldine salt was prepared by a novel emulsion polymerization pathway using dodecylbenzene sulfonic acid and sulfuric acid together as dopants. The effect of temperature and heating rate on the degradation of this emeraldine salt was studied via thermogravimetric analysis. The thermally analyzed sample was collected at various temperatures, that is, 250, 490, 500, and 1000°C. The gradual changes in the structure of the emeraldine salt were followed through cyclic voltammetry, Fourier transform infrared spectroscopy, and ultraviolet-visible spectroscopy. Results demonstrate that emeraldine salt shows high thermal stability up to 500°C. This is much higher working temperature for the use of emeraldine salt in higher temperature applications. Further heat treatment seems to induce deprotonation in emeraldine salt. Cyclic voltammetry and ultraviolet-visible spectroscopy revealed that complete deprotonation takes place at 1000°C where it loses its electrical conductivity. It is interesting to note that after the elimination of the dopants, the basic backbone of emeraldine salt was not destroyed. The results reveal that the dopants employed have a stability effect on the skeleton of emeraldine salt.

THE EFFECT OF TEMPERATURE ON THE RATE AND VARIATION OF OPERCULAR MOVEMENT IN FUNDULUS DIAPHANUS DIAPHANUS

1947 ◽  
Vol 25d (2) ◽  
pp. 91-95
Author(s):  
Benjamin N. Kropp
Keyword(s):  
Constant Temperature ◽  
Beat Frequency ◽  
Nervous Activity ◽  
Respiratory Movement ◽  
Effect Of Temperature ◽  
Temperature Range ◽  
Sources Of Variation ◽  
Fundulus Diaphanus

The rates of opercular beat of 16 specimens of Fundulus diaphanus diaphanus were recorded over a temperature range from 4.3° to 17.5 °C. in order to determine how this respiratory movement varied with temperature and some of the sources of variation in rate. While the rate of beat varies directly as the temperature, over a period of several hours at any constant temperature continuous recordings of the rate show recurring cycles of rise and fall in beat frequency that are chiefly responsible for the scatter of the observations. Both the duration of a cycle and the limits of rise and fall for each cycle are definitely set by the temperature. The possible dependence of these phenomena upon central nervous activity is discussed.

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