Tail Beat Frequency Research Articles

Optimal Strouhal number for swimming animals

To evaluate the swimming performances of aquatic animals, an important dimensionless quantity is the Strouhal number, St=fA/U, with f the tail-beat frequency, A the peak-to-peak tail amplitude, and U the swimming velocity. Experiments with flapping foils have exhibited maximum propulsive efficiency in the interval 0.25<St<0.35 and it has been argued that animals likely evolved to swim in the same narrow interval. Using Lighthill's elongated-body theory to address undulatory propulsion, it is demonstrated here that the optimal Strouhal number increases from 0.15 to 0.8 for animals spanning from the largest cetaceans to the smallest tadpoles. To assess the validity of this model, the swimming kinematics of 53 different species of aquatic animals have been compiled from the literature and it shows that their Strouhal numbers are consistently near the predicted optimum.

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

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 Ucritprotocol. TBF was more variable between individuals swimming at the same speed within the Ucritcompared with the endurance protocol. Finally, a significant negative correlation was found between TBF and Ucritin individual fish, suggesting that station-holding may be an important energy saving strategy during swimming in this size class of sturgeon.

Fluid dynamics of moving fish in a two-dimensional multiparticle collision dynamics model

The fluid dynamics of animal locomotion, such as that of an undulating fish, are of great interest to both biologists and engineers. However, experimentally studying these fluid dynamics is difficult and time consuming. Model studies can be of great help because of their simpler and more detailed analysis. Their insights may guide empirical work. Particularly the recently introduced multiparticle collision dynamics method may be suitable for the study of moving organisms because it is computationally fast, simple to implement, and has a continuous representation of space. As regards the study of hydrodynamics of moving organisms, the method has only been applied at low Reynolds numbers (below 120) for soft, permeable bodies, and static fishlike shapes. In the present paper we use it to study the hydrodynamics of an undulating fish at Reynolds numbers 1100-1500, after confirming its performance for a moving insect wing at Reynolds number 75. We measure (1) drag, thrust, and lift forces, (2) swimming efficiency and spatial structure of the wake, and (3) distribution of forces along the fish body. We confirm the resemblance between the simulated undulating fish and empirical data. In contrast to theoretical predictions, our model shows that for steadily undulating fish, thrust is produced by the rear 2/3 of the body and that the slip ratio U/V (with U the forward swimming speed and V the rearward speed of the body wave) correlates negatively (instead of positively) with the actual Froude efficiency of swimming. Besides, we show that the common practice of modeling individuals while constraining their sideways acceleration causes them to resemble unconstrained fish with a higher tailbeat frequency.

Wake structures behind a swimming robotic lamprey with a passively flexible tail.

A robotic lamprey, based on the silver lamprey, Ichthyomyzon unicuspis, was used to investigate the influence of passive tail flexibility on the wake structure and thrust production during anguilliform swimming. A programmable microcomputer actuated 11 servomotors that produce a traveling wave along the length of the lamprey body. The waveform was based on kinematic studies of living lamprey, and the shape of the tail was taken from a computer tomography scan of the silver lamprey. The tail was constructed of flexible PVC gel, and nylon inserts were used to change its degree of flexibility. Particle image velocimetry measurements using three different levels of passive flexibility show that the large-scale structure of the wake is dominated by the formation of two pairs of vortices per shedding cycle, as seen in the case of a tail that flexed actively according to a pre-defined kinematic pattern, and did not bend in response to fluid forces. When the tail is passively flexible, however, the large structures are composed of a number of smaller vortices, and the wake loses coherence as the degree of flexibility increases. Momentum balance calculations indicate that, at a given tailbeat frequency, increasing the tail flexibility yields less net force, but changing the cycle frequency to match the resonant frequency of the tail increases the force production.

입자영상유속계를 이용한 은어 (Plecoglossus altivelis)의 유영능력 측정

As a fish way is a structure for fish migrating well toward upper stream due to breaking river flow by a dam or dammed pool, the specific fish's swimming ability is one of the main factors in making a plan and managing it. In addition, it also needs to understand the current field in fish road to evaluate its performance. This study is aimed to analyze the swimming patterns with current velocity changes using a Particle Imaging Velocimetry (PIV) in order to understand the swimming ability of silver fish (Plecoglossus altivelis) that is one of the fishes migrating through the fish way of Nakdong River, and to analyze the 2 dimensional current field near to silver fish at swimming momentum. The results showed that average values of tail beat frequencies for continuous swimming with current velocity were 2.8 Hz at 0.3 m/s, 3.2 Hz at 0.4 m/s, 3.8 Hz at 0.5 m/s, respectively. The wake would be produced by direction turning of fish's tail fin and its magnitude would be verified by the difference of pressure. The pressure turbulent flow produced by its tail beat would be made in both sides, and then, the magnitude of wake should be the source of moving direction. The swimming momentum will help to support the primary factor in making a suitable design for specific fish species migrating toward the district river.

Swim performance and energy homeostasis in spottail shiner ( Notropis hudsonius) collected downstream of a uranium mill

The Key Lake uranium milling operation (Saskatchewan, Canada) releases complex effluent into the local watershed. The objective of the current study was to investigate whether fish from an effluent-receiving waterbody exhibited differences in swimming performance and energy homeostasis compared to fish from a local reference site. Juvenile spottail shiner ( Notropis hudsonius) were collected from a lake downstream of the uranium mill, and compared to fish collected from a nearby reference lake. Critical swimming speed ( U crit; fatigue velocity), tail beat frequency, and tail amplitude did not differ significantly when comparing fish collected from the exposure lake and reference lake. Captured shiner used in swim tests were considered fatigued, and metabolic endpoints were compared between this group and non-fatigued fish, which were treated similarly but not subjected to swim tests. In both non-fatigued and fatigued shiner, liver glycogen was significantly greater in fish collected from the exposure lake compared to the reference lake. However, it is unclear if this effect, and others related to condition, were the result of contaminant exposure or other environmental factors. While there were no differences in plasma lactate, hematocrit or liver triglycerides in non-fatigued fish between sites, only fatigued reference fish had increased lactate and hematocrit and decreased triglycerides. In non-fatigued fish, plasma glucose did not significantly differ between sites, but significantly decreased after swimming only in fish from the exposure lake. In summary, shiner from the exposure site demonstrated similar swim endurance and possessed greater energy stores despite metabolic alterations compared to shiner from the reference site. Therefore, because fish collected downstream of the uranium mill operation had similar swimming ability as fish from the reference lake, U crit test results presented here may not reflect or be indicative of metabolic effects of complex effluent exposure.

Movement and function of the pectoral fins of the larval zebrafish (Danio rerio) during slow swimming

Pectoral fins are known to play important roles in swimming for many adult fish; however, their functions in fish larvae are unclear. We examined routine pectoral fin movement during rhythmic forward swimming and used genetic ablation to test hypotheses of fin function in larval zebrafish. Fins were active throughout bouts of slow swimming. Initiation was characterized by asymmetric fin abduction that transitioned to alternating rhythmic movement with first fin adduction. During subsequent swimming, fin beat amplitude decreased while tail beat amplitude increased over swimming speeds ranging from 1.47 to 4.56 body lengths per second. There was no change in fin or tail beat frequency with speed (means ± s.d.: 28.2±3.5 and 29.6±1.9 Hz, respectively). To examine potential roles of the pectoral fins in swimming, we compared the kinematics of finless larvae generated with a morpholino knockdown of the gene fgf24 to those of normal fish. Pectoral fins were not required for initiation nor did they significantly impact forward rhythmic swimming. We investigated an alternative hypothesis that the fins function in respiration. Dye visualization demonstrated that pectoral fin beats bring distant fluid toward the body and move it caudally behind the fins, disrupting the boundary layer along the body's surface, a major site of oxygen absorption in larvae. Larval zebrafish also demonstrated more fin beating in low oxygen conditions. Our data reject the hypothesis that the pectoral fins of larval zebrafish have a locomotor function during slow, forward locomotion, but are consistent with the hypothesis that the fins have a respiratory function.

Aerobic swimming performance of juvenile Schizothorax chongi (Pisces, Cyprinidae) in the Yalong River, southwestern China

Schizothorax chongi (locally known as Xilian Yu), a fish species commonly found in Yalong River, has been declining quickly in recent years. One of the important factors, among many, is the interruption of the free flowing river by dams. To obtain data that can be applied to the design of a fishway for S. chongi and other species in the community, a laboratory study of juvenile S. chongi’s swimming energetics and kinematics was conducted in a flume-type respirometer equipped with a high speed video camera system to record swimming behavior. The aerobic metabolic rate, tail beat frequency (TBF) and tail beat amplitude (TBA) were measured during steady swimming at varying flow rates for fish of similar mass. A power function accurately describes the relationship between oxygen consumption rate (MO2) and swimming speed (U). The estimated standard metabolic rate (SMR) calculated from the power function was 445.34 mg O2 kg−1 h−1, similar to the experimental result of 431.5 mg O2 kg−1 h−1. The relationship between cost of transport (COT) and U was, characteristically, inverse bell-shaped, with COTmin = 44.6 J kg−1 m−1 at Uopt = 5.5 body lengths per second (bl s−1). There was a significant positive linear correlation between TBF and U. The slope of the correlation (0.33) was lower than for many other species, implying that S. chongi swim efficiently. The TBA, ranging from 0.15 to 0.2 bl, was found to be independent of U. Kinematic analyses indicates that S. chongi primarily depends on the caudal fin to generate forward thrust and employs three velocity-dependent swimming gaits. This investigation provides data on the swimming ability of S. chongi that will add to the basic science required for fishway design.

Use of Sand Ripples to Enhance Chafing in Caribbean Reef Sharks (Carcharhinus Perezi) and Blacktip Sharks (Carcharhinus Limbatus)

Although chafing-the rubbing of a body on the sea floor-is a common response of sharks to the attachment of irritating sharksuckers (Echeneis spp.), this behavior has not yet been analyzed in detail. I focused on the different forms and functions of chafing, with special emphasis on the use of sand ripples by sharks during chafing. A significant number of the 146 videotaped Caribbean reef sharks, Carcharhinus perezi (Poey, 1876), and blacktip sharks, Carcharhinus limbatus (Muller and Henle, 1839), preferred to chafe against sand ripples with either a parallel or perpendicular swim direction rather than a transverse swim direction. Tailbeat frequencies of the different forms of the chafing behavior were significantly larger than cruising frequencies. Results indicate that successful chafing requires that sharks employ pattern-recognition and body awareness during chafing

Pop up satellite tags impair swimming performance and energetics of the European eel (Anguilla anguilla).

Pop-up satellite archival tags (PSATs) have recently been applied in attempts to follow the oceanic spawning migration of the European eel. PSATs are quite large, and in all likelihood their hydraulic drag constitutes an additional cost during swimming, which remains to be quantified, as does the potential implication for successful migration. Silver eels (LT = 598.6±29 mm SD, N = 9) were subjected to swimming trials in a Steffensen-type swim tunnel at increasing speeds of 0.3–0.9 body lengths s−1, first without and subsequently with, a scaled down PSAT dummy attached. The tag significantly increased oxygen consumption (MO2) during swimming and elevated minimum cost of transport (COTmin) by 26%. Standard (SMR) and active metabolic rate (AMR) as well as metabolic scope remained unaffected, suggesting that the observed effects were caused by increased drag. Optimal swimming speed (U opt) was unchanged, whereas critical swimming speed (U crit) decreased significantly. Swimming with a PSAT altered swimming kinematics as verified by significant changes to tail beat frequency (f), body wave speed (v) and Strouhal number (St). The results demonstrate that energy expenditure, swimming performance and efficiency all are significantly affected in migrating eels with external tags.

Thrust Analysis of a Fish Robot Actuated by Piezoceramic Composite Actuators

In this work, a three-dimensional (3D) Computational Fluid Dynamics (CFD) model was built to simulate the tail fin motion of a fish robot actuated by a piezoceramic composite actuator, and to determine the maximum thrust tail-beat frequency. A simulation of the tail fin at a tail-beat frequency was performed to confirm measured thrust data from a previous study. The computed and measured thrusts were in good agreement. A series of thrust simulations were conducted for various tail-beat frequencies to confirm the maximum thrust frequency that was obtained from thrust measurements in the previous study. The largest thrust was calculated at a tail-beat frequency of 3.7 Hz and vortices around the tail were fully separated. The calculated maximum thrust tail-beat frequency was in good agreement with the measured frequency. Flow characteristics during tail fin motion were examined to explain why the largest thrust occurred at this particular tail-beat frequency.

Testing Biomimetic Structures in Bioinspired Robots: How Vertebrae Control the Stiffness of the Body and the Behavior of Fish-Like Swimmers

Our goal is to describe a specific case of a general process gaining traction amongst biologists: testing biological hypotheses with biomimetic structures that operate in bioinspired robots. As an example, we present MARMT (mobile autonomous robot for mechanical testing), a surface-swimmer that undulates a submerged biomimetic tail to power cruising and accelerations. Our goal was to test the hypothesis that stiffness of the body controls swimming behavior and that both stiffness and behavior can be altered by changes in the morphology of the vertebral column. To test this hypothesis, we built biomimetic vertebral columns (BVC) outfitted with variable numbers of rigid ring centra; as the number of centra increased the axial length of the intervertebral joints decreased. Each kind of BVC was tested in dynamic bending to measure the structure's apparent stiffness as the storage and loss moduli. In addition, each kind of BVC was used as the axial skeleton in a tail that propelled MARMT. We varied MARMT's tail-beat frequency, lateral amplitude of the tail, and swimming behavior. MARMT's locomotor performance was measured using an on-board accelerometer and external video. As the number of vertebrae in the BVC of fixed length increased, so, too, did the BVC's storage modulus, the BVC's loss modulus, MARMT's mean speed during cruising, and MARMT's peak acceleration during a startle response. These results support the hypothesis that stiffness of the body controls swimming behavior and that both stiffness and behavior can be altered by changes in the morphology of the vertebral column.

Acute exposure to 2,4-dinitrophenol alters zebrafish swimming performance and whole body triglyceride levels

While swimming endurance (critical swimming speed or U crit) and lipid stores have both been reported to acutely decrease after exposure to a variety of toxicants, the relationship between these endpoints has not been clearly established. In order to examine these relationships, adult zebrafish ( Danio rerio) were aqueously exposed to solvent control (ethanol) or two nominal concentrations of 2,4-dinitrophenol (DNP), a mitochondrial electron transport chain uncoupler, for a 24-h period. Following exposure, fish were placed in a swim tunnel in clean water for swimming testing or euthanized immediately without testing, followed by analysis of whole body triglyceride levels. U crit decreased in both the 6 mg/L and 12 mg/L DNP groups, with 12 mg/L approaching the LC 50. A decrease in tail beat frequency was observed without a significant change in tail beat amplitude. In contrast, triglyceride levels were elevated in a concentration-dependent manner in the DNP exposure groups, but only in fish subjected to swimming tests. This increase in triglyceride stores may be due to a direct interference of DNP on lipid catabolism as well as increased triglyceride production when zebrafish were subjected to the co-stressors of swimming and toxicant exposure. Future studies should be directed at determining how acute DNP exposure combines with swimming to cause alterations in triglyceride accumulation.

Yo-yo vertical movements suggest a foraging strategy for tiger sharks Galeocerdo cuvier

Many pelagic fishes exhibit ‘yo-yo’ diving behavior, which may serve several possible functions, including energy conservation, prey searching and navigation. We deployed accelerometers and digital still cameras on 4 free-ranging tiger sharks Galeocerdo cuvier, to test whether their vertical movements are most consistent with energy conservation or prey searching. All sharks swam continuously, with frequent vertical movements through the water column at mean swimming speeds of 0.5 to 0.9 m s–1. Tail-beating was continuous except for sporadic, powerless gliding during descents (from 0 to 18% of total descent time). At a given tailbeat frequency, swimming speeds were lower during ascent than descent (consistent with negative buoyancy). Burst swimming events, which might represent prey pursuits, were observed during all phases of vertical movements. Camera images showed a variety of potential prey and the possible capture of a unicornfish. Collectively, results suggest that yo-yo diving by tiger sharks is not primarily for energy conservation, but probably represents an effective search strategy for locating prey throughout the water column.

Dietary selenomethionine exposure in adult zebrafish alters swimming performance, energetics and the physiological stress response

Selenomethionine (Se-Met) is the major form of organoselenium present in food. Early life stages of oviparous vertebrate species, especially fish, are highly susceptible to dietary selenium (Se) exposure; however less is known concerning effects in adults. The present study was designed to investigate behavioral and physiological consequences of dietary Se-Met exposure to adult zebrafish ( Danio rerio). Adult fish were fed either control food (1.3 μg Se/g, dry weight or dw) or food spiked with varying measured concentrations of Se (3.7, 9.6 and 26.6 μg Se/g, dw) in the form of Se-Met for 60 days at 5% body weight/day ration, and an additional 30–40 days with equal ration (2.5%) of control or Se-Met spiked foods and clean chironomids. At the end of the exposure period, critical swimming speed (Ucrit), oxygen consumption (MO 2), cost of transport (COT), tail beat amplitude, tail beat frequency, and whole body cortisol, triglyceride and glycogen levels were determined. Significantly reduced Ucrit was observed in fish fed 3.7, 9.6 and 26.6 μg Se/g when compared to control fish. Although MO 2 of fish fed >3 μg Se/g was consistently greater than control fish, those values were not statistically significant. There was no difference in COT among different treatment groups. Tail beat amplitudes of fish fed >3 μg Se/g were lower than control fish, however tail beat frequencies were not altered. Fish fed 3.7, 9.6 and 26.6 μg Se/g had greater whole body triglycerides and glycogen levels than control fish. Fish fed the highest concentration of Se (26.6 μg Se/g) had elevated levels of whole body cortisol compared to control fish. Our results suggest that environmentally relevant dietary Se-Met exposure can alter both behavioral and physiological responses in adult fish, and such consequences could threaten fitness of adult fish in Se impacted aquatic ecosystems.

Adaptive Locomotor Behavior in Larval Zebrafish

In this study we report that larval zebrafish display adaptive locomotor output that can be driven by unexpected visual feedback. We develop a new assay that addresses visuomotor integration in restrained larval zebrafish. The assay involves a closed-loop environment in which the visual feedback a larva receives depends on its own motor output in a way that resembles freely swimming conditions. The experimenter can control the gain of this closed feedback loop, so that following a given motor output the larva experiences more or less visual feedback depending on whether the gain is high or low. We show that increases and decreases in this gain setting result in adaptive changes in behavior that lead to a generalized decrease or increase of motor output, respectively. Our behavioral analysis shows that both the duration and tail beat frequency of individual swim bouts can be modified, as well as the frequency with which bouts are elicited. These changes can be implemented rapidly, following an exposure to a new gain of just 175 ms. In addition, modifications in some behavioral parameters accumulate over tens of seconds and effects last for at least 30 s from trial to trial. These results suggest that larvae establish an internal representation of the visual feedback expected from a given motor output and that the behavioral modifications are driven by an error signal that arises from the discrepancy between this expectation and the actual visual feedback. The assay we develop presents a unique possibility for studying visuomotor integration using imaging techniques available in the larval zebrafish.

Interactions between internal forces, body stiffness, and fluid environment in a neuromechanical model of lamprey swimming.

Animal movements result from a complex balance of many different forces. Muscles produce force to move the body; the body has inertial, elastic, and damping properties that may aid or oppose the muscle force; and the environment produces reaction forces back on the body. The actual motion is an emergent property of these interactions. To examine the roles of body stiffness, muscle activation, and fluid environment for swimming animals, a computational model of a lamprey was developed. The model uses an immersed boundary framework that fully couples the Navier-Stokes equations of fluid dynamics with an actuated, elastic body model. This is the first model at a Reynolds number appropriate for a swimming fish that captures the complete fluid-structure interaction, in which the body deforms according to both internal muscular forces and external fluid forces. Results indicate that identical muscle activation patterns can produce different kinematics depending on body stiffness, and the optimal value of stiffness for maximum acceleration is different from that for maximum steady swimming speed. Additionally, negative muscle work, observed in many fishes, emerges at higher tail beat frequencies without sensory input and may contribute to energy efficiency. Swimming fishes that can tune their body stiffness by appropriately timed muscle contractions may therefore be able to optimize the passive dynamics of their bodies to maximize peak acceleration or swimming speed.

Behavioural responses to pressure changes in cultured Atlantic cod ( Gadus morhua): Defining practical limits for submerging and lifting sea-cages

Farmed Atlantic cod ( Gadus morhua) are occasionally exposed to buoyancy changes in sea-cages, through lifting or lowering of cage nets. Physiological processes regulate the level of gas in the closed swim bladders of cod and thus the ability of cod to control their buoyancy. Rapid net lifting may cause positive buoyancy, leading to barotrauma, while net lowering may lead to negative buoyancy and alter cod behaviours. We tested how groups of farmed cod responded immediately after lifting events from 5 different start depths equivalent to 40% pressure reductions, and how long they took to return to pre-lifting pressure levels. In addition, we tested immediate responses and recovery times to cage lowering events equivalent to 100–300% pressure increases. Trials were conducted with 100 cod of 1.1–1.7 kg in a 63 m 3 sea-cage at the lower (5 °C) and upper (16 °C) water temperature limits experienced during culture. Swimming behaviours were measured at fixed intervals before and after cage lifting or lowering, and a feeding test was used to assess appetite. In general, lifting events increased swimming speeds 1.5–4 times and tail beats 2–3 times and fish swam with an average −14° head-down angle, indicating positive buoyancy. The depth before lifting affected the immediate response as the fish became more active after lifting events from shallow compared to deeper depths. Appetite levels decreased for about 2 h after cage lifting, independent of temperature or start depth. The overall recovery time of 8 h after lifting did not depend upon start depth or temperature. Lowering events appeared to cause negative buoyancy. Swimming speeds (1.3–2.3 times) and tail beat frequencies (1.4–2.3 times) increased immediately after cage lowering, and cod swam with an average 30° head-up swimming angle. Neither pressure level nor temperature affected this immediate response. Time to recover to neutral buoyancy for 300% pressure increases took 42–90 h, but only 18–34 h for 100% pressure increases. We conclude that a 40% pressure reduction is an upper limit for lifts of healthy farmed cod. Secondary lifts should not be done until at least 10 h after the first lift. Cage lowering should be done slowly to avoid potentially stressful crowding of negatively buoyant fish on the cage bottom, especially at low temperatures.

Sublethal Effects of Ammoniacal Fertilizer Effluents on three Commercial Fish Species from Niger Delta Area, Nigeria

Sublethal effects of various concentrations of fertilizer effluents on the tail beat frequency per minute (TBF min.-1) and opercular beat frequency per minute. (OBF min-1) of Orechromis niloticus, Clarias gariepinus and hybrid (Heterobranchus bidorsalis (female) x C. gariepinus (male)) were examined in a static 96hr. bioassay under laboratory conditions. Effluent concentration, ammmonia (ionised and un-ionised), urea and pH significantly affected TBF and OBF of the three species. Ammonia particularly, the un-ionised form exacted the most significant effect onTBF and OBF. OBF appears be a more sensitive indicator of stress than TBF and may therefore be more suitable for detecting sublethal physiological effects of pollutants. This study further revealed that the fertilizer effluents have variable compositions whose values may far exceed the allowable limits and hence may pose great danger to the aquaticenvironment.

Tail‐Beat Patterns in Dual‐Frequency Identification Sonar Echograms and their Potential Use for Species Identification and Bioenergetics Studies

AbstractWe observed patterns in echograms of data collected with a dual‐frequency identification sonar (DIDSON) that were related to the tail beats of fish. These patterns reflect the size, shape, and swimming motion of the fish and also depend on the fish's angle relative to the axis of the beam. When the tail is large enough to reflect sound of sufficient intensity and the body is angled such that the tail beat produces periodic changes in the range extent covered by the fish image, then the tail beat becomes clearly visible on echograms that plot the intensity maximum of all beams. The analysis of DIDSON echograms of a mix of upstream‐migrating Chinook salmon Oncorhynchus tshawytscha and sockeye salmon O. nerka resulted in the separation of two groups: (1) fish of sockeye salmon size that swam with a tail‐beat frequency (TBF) between 2.0 and 3.5 beats/s and (2) fish of Chinook salmon size with a TBF between 1.0 and 2.0 beats/s. There was no correlation between TBF and fish size within each group, which suggests that the observed difference in TBF between the two groups was species‐specific rather than an indirect effect of the groups' difference in size. The technique of extracting TBF from DIDSON echograms may also be useful for bioenergetics studies. Compared with electromyogram telemetry, it offers the advantages of being nonintrusive and faster to set up and analyze and therefore is suitable for analyzing larger sample sizes. The disadvantages are that the technique's potential is limited to relatively large fish, it can cover only relatively small areas, it cannot be used to follow individual fish over long distances, and some environments are too noisy to produce DIDSON images of sufficient quality.