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Sample records for labriform swimming fish

  1. Unsteady flow affects swimming energetics in a labriform fish (Cymatogaster aggregata).

    PubMed

    Roche, D G; Taylor, M K; Binning, S A; Johansen, J L; Domenici, P; Steffensen, J F

    2014-02-01

    Unsteady water flows are common in nature, yet the swimming performance of fishes is typically evaluated at constant, steady speeds in the laboratory. We examined how cyclic changes in water flow velocity affect the swimming performance and energetics of a labriform swimmer, the shiner surfperch, Cymatogaster aggregata, during station holding. Using intermittent-flow respirometry, we measured critical swimming speed (Ucrit), oxygen consumption rates (O2) and pectoral fin use in steady flow versus unsteady flows with either low- [0.5 body lengths (BL) s(-1)] or high-amplitude (1.0 BL s(-1)) velocity fluctuations, with a 5 s period. Individuals in low-amplitude unsteady flow performed as well as fish in steady flow. However, swimming costs in high-amplitude unsteady flow were on average 25.3% higher than in steady flow and 14.2% higher than estimated values obtained from simulations based on the non-linear relationship between swimming speed and oxygen consumption rate in steady flow. Time-averaged pectoral fin use (fin-beat frequency measured over 300 s) was similar among treatments. However, measures of instantaneous fin use (fin-beat period) and body movement in high-amplitude unsteady flow indicate that individuals with greater variation in the duration of their fin beats were better at holding station and consumed less oxygen than fish with low variation in fin-beat period. These results suggest that the costs of swimming in unsteady flows are context dependent in labriform swimmers, and may be influenced by individual differences in the ability of fishes to adjust their fin beats to the flow environment.

  2. A hydrodynamic analysis of fish swimming speed: wake structure and locomotor force in slow and fast labriform swimmers.

    PubMed

    Drucker, E G; Lauder, G V

    2000-08-01

    Past study of interspecific variation in the swimming speed of fishes has focused on internal physiological mechanisms that may limit the ability of locomotor muscle to generate power. In this paper, we approach the question of why some fishes are able to swim faster than others from a hydrodynamic perspective, using the technique of digital particle image velocimetry which allows measurement of fluid velocity and estimation of wake momentum and mechanical forces for locomotion. We investigate the structure and strength of the wake in three dimensions to determine how hydrodynamic force varies in two species that differ markedly in maximum swimming speed. Black surfperch (Embiotoca jacksoni) and bluegill sunfish (Lepomis macrochirus) swim at low speeds using their pectoral fins exclusively, and at higher speeds switch to combined pectoral and caudal fin locomotion. E. jacksoni can swim twice as fast as similarly sized L. macrochirus using the pectoral fins alone. The pectoral fin wake of black surfperch at all speeds consists of two distinct vortex rings linked ventrally. As speed increases from 1.0 to 3.0 L s(-)(1), where L is total body length, the vortex ring formed on the fin downstroke reorients to direct force increasingly downstream, parallel to the direction of locomotion. The ratio of laterally to downstream-directed force declines from 0.93 to 0.07 as speed increases. In contrast, the sunfish pectoral fin generates a single vortex ring per fin beat at low swimming speeds and a pair of linked vortex rings (with one ring only partially complete and attached to the body) at maximal labriform speeds. Across a biologically relevant range of swimming speeds, bluegill sunfish generate relatively large lateral forces with the paired fins: the ratio of lateral to downstream force remains at or above 1.0 at all speeds. By increasing wake momentum and by orienting this momentum in a direction more favorable for thrust than for lateral force, black surfperch are able

  3. Labriform swimming of a ray-strengthened pectoral fin

    NASA Astrophysics Data System (ADS)

    Shoele, Kourosh; Zhu, Qiang

    2009-11-01

    Labriform swimming is a common locomotion mode used by fish in low speed swimming, in which thrust generation is achieved through a combination of flapping and rowing motions of pectoral fins. Pectoral fins of bony fishes usually consist of a soft collagen membrane strengthened by embedded flexible rays. Morphologically, each ray is connected to a group of muscles so that the fish can control the rotational motion of each ray individually, enabling multi-degree of freedom control over the fin motion and deformation. We have developed a fluid-structure interaction model to simulate the kinematics and dynamic performance of a structurally idealized fin. This method includes a boundary-element model of the fluid motion and a fully-nonlinear Euler-Bernoulli beam model of the embedded rays. Using this model we studied thrust generation and propulsion efficiency of the fin at different combinations of parameters. Effects of kinematic as well as structural properties are examined. It has been illustrated that the fish's capacity to control the motion of each individual ray, as well as the anisotropic deformability of the fin determined by distribution of the rays, are essential to high propulsion performance. Specifically, it is found that a reinforced ray at the leading edge leads to performance enhancement.

  4. Partition of aerobic and anaerobic swimming costs related to gait transitions in a labriform swimmer.

    PubMed

    Svendsen, Jon C; Tudorache, Christian; Jordan, Anders D; Steffensen, John F; Aarestrup, Kim; Domenici, Paolo

    2010-07-01

    Members of the family Embiotocidae exhibit a distinct gait transition from exclusively pectoral fin oscillation to combined pectoral and caudal fin propulsion with increasing swimming speed. The pectoral-caudal gait transition occurs at a threshold speed termed U(p-c). The objective of this study was to partition aerobic and anaerobic swimming costs at speeds below and above the U(p-c) in the striped surfperch Embiotoca lateralis using swimming respirometry and video analysis to test the hypothesis that the gait transition marks the switch from aerobic to anaerobic power output. Exercise oxygen consumption rate was measured at 1.4, 1.9 and 2.3 L s(-1). The presence and magnitude of excess post-exercise oxygen consumption (EPOC) were evaluated after each swimming speed. The data demonstrated that 1.4 L s(-1) was below the U(p-c), whereas 1.9 and 2.3 L s(-1) were above the U(p-c). These last two swimming speeds included caudal fin propulsion in a mostly steady and unsteady (burst-assisted) mode, respectively. There was no evidence of EPOC after swimming at 1.4 and 1.9 L s(-1), indicating that the pectoral-caudal gait transition was not a threshold for anaerobic metabolism. At 2.3 L s(-1), E. lateralis switched to an unsteady burst and flap gait. This swimming speed resulted in EPOC, suggesting that anaerobic metabolism constituted 25% of the total costs. Burst activity correlated positively with the magnitude of the EPOC. Collectively, these data indicate that steady axial propulsion does not lead to EPOC whereas transition to burst-assisted swimming above U(p-c) is associated with anaerobic metabolism in this labriform swimmer.

  5. Synchronized Swimming of Two Fish

    NASA Astrophysics Data System (ADS)

    Koumoutsakos, Petros; Novati, Guido; Abbati, Gabriele; Hejazialhosseini, Babak; van Rees, Wim

    2015-11-01

    We present simulations of two, self-propelled, fish-like swimmers that perform synchronized moves in a two-dimensional, viscous fluid. The swimmers learn to coordinate by receiving a reward for their synchronized actions. We analyze the swimming patterns emerging for different rewards in terms of their hydrodynamic efficiency and artistic impression. European Research Council (ERC) Advanced Investigator Award (No. 2-73985-14).

  6. Emulating a Fish Swim Bladder

    NASA Astrophysics Data System (ADS)

    Vesenka, James; Meredith, Dawn; Bolker, Jessica; Schubert, Christopher; Kraut, Gertrud

    2009-10-01

    The University of New Hampshire and the University of New England are developing biologically relevant physics laboratories for their predominantly health science audiences. Buoyancy plays an important role in a variety of biological processes. We describe an inexpensive laboratory activity based on the Cartesian Diver that allows students to quantitatively emulate the swim bladder of a fish. Inflation of the ``bladder'' is externally controlled through an external gas syringe or squeezing on the plastic water containment vessel (a 2L soda bottle). The students can accurately determine the volume of a ``fish'' at the point of neutral buoyancy by visual measurement of the trapped air pocket. A simple electronic gas pressure sensor allows the hydrostatic pressure on the fish to be analyzed simultaneously.

  7. Center of mass motion in swimming fish: effects of speed and locomotor mode during undulatory propulsion.

    PubMed

    Xiong, Grace; Lauder, George V

    2014-08-01

    Studies of center of mass (COM) motion are fundamental to understanding the dynamics of animal movement, and have been carried out extensively for terrestrial and aerial locomotion. But despite a large amount of literature describing different body movement patterns in fishes, analyses of how the center of mass moves during undulatory propulsion are not available. These data would be valuable for understanding the dynamics of different body movement patterns and the effect of differing body shapes on locomotor force production. In the present study, we analyzed the magnitude and frequency components of COM motion in three dimensions (x: surge, y: sway, z: heave) in three fish species (eel, bluegill sunfish, and clown knifefish) swimming with four locomotor modes at three speeds using high-speed video, and used an image cross-correlation technique to estimate COM motion, thus enabling untethered and unrestrained locomotion. Anguilliform swimming by eels shows reduced COM surge oscillation magnitude relative to carangiform swimming, but not compared to knifefish using a gymnotiform locomotor style. Labriform swimming (bluegill at 0.5 body lengths/s) displays reduced COM sway oscillation relative to swimming in a carangiform style at higher speeds. Oscillation frequency of the COM in the surge direction occurs at twice the tail beat frequency for carangiform and anguilliform swimming, but at the same frequency as the tail beat for gymnotiform locomotion in clown knifefish. Scaling analysis of COM heave oscillation for terrestrial locomotion suggests that COM heave motion scales with positive allometry, and that fish have relatively low COM oscillations for their body size. Copyright © 2014 Elsevier GmbH. All rights reserved.

  8. The effects of acute temperature change on swimming performance in bluegill sunfish Lepomis macrochirus.

    PubMed

    Jones, Emily A; Jong, Arianne S; Ellerby, David J

    2008-05-01

    Many fish change gait within their aerobically supported range of swimming speeds. The effects of acute temperature change on this type of locomotor behavior are poorly understood. Bluegill sunfish swim in the labriform mode at low speeds and switch to undulatory swimming as their swimming speed increases. Maximum aerobic swimming speed (U(max)), labriform-undulatory gait transition speed (U(trans)) and the relationships between fin beat frequency and speed were measured at 14, 18, 22, 26 and 30 degrees C in bluegill acclimated to 22 degrees C. At temperatures below the acclimation temperature (T(a)), U(max), U(trans) and the caudal and pectoral fin beat frequencies at these speeds were reduced relative to the acclimation level. At temperatures above T(a) there was no change in these variables relative to the acclimation level. Supplementation of oxygen levels at 30 degrees C had no effect on swimming performance. The mechanical power output of the abductor superficialis, a pectoral fin abductor muscle, was measured in vitro at the same temperatures used for the swimming experiments. At and below T(a), maximal power output was produced at a cycle frequency approximately matching the in vivo pectoral fin beat frequency. At temperatures above T(a) muscle power output and cycle frequency could be increased above the in vivo levels at U(trans). Our data suggest that the factors triggering the labriform-undulatory gait transition change with temperature. Muscle mechanical performance limited labriform swimming speed at T(a) and below, but other mechanical or energetic factors limited labriform swimming speed at temperatures above T(a).

  9. Swimming Performance of Toy Robotic Fish

    NASA Astrophysics Data System (ADS)

    Petelina, Nina; Mendelson, Leah; Techet, Alexandra

    2015-11-01

    HEXBUG AquaBotsTM are a commercially available small robot fish that come in a variety of ``species''. These models have varying caudal fin shapes and randomly-varied modes of swimming including forward locomotion, diving, and turning. In this study, we assess the repeatability and performance of the HEXBUG swimming behaviors and discuss the use of these toys to develop experimental techniques and analysis methods to study live fish swimming. In order to determine whether these simple, affordable model fish can be a valid representation for live fish movement, two models, an angelfish and a shark, were studied using 2D Particle Image Velocimetry (PIV) and 3D Synthetic Aperture PIV. In a series of experiments, the robotic fish were either allowed to swim freely or towed in one direction at a constant speed. The resultant measurements of the caudal fin wake are compared to data from previous studies of a real fish and simplified flapping propulsors.

  10. Swimming Efficiently: An Analytical Study of Optimal Swimming in Fish

    NASA Astrophysics Data System (ADS)

    Wiens, A. Josh; Hosoi, Anette

    2014-11-01

    The Strouhal Number (St) , is widely considered to be the defining parameter for efficient undulatory swimming. Biological studies have shown that fish species across a broad range of shapes and sizes adhere to a narrow St range (0 . 2 < St < 0 . 4). Despite its significance, St alone provides an incomplete description of the kinematics and geometry of a swimming fish. The dimensionless speed and amplitude of the body wave, along with the size and shape of the body can also play a significant role in swimming performance. We apply Lighthill's elongated body theory to construct a simple but powerful reduction of the steady-swimming problem. Through this reduction, the energetic efficiency of a swimming fish can be directly expressed as an analytical function of body geometry and kinematics. In this reduced form, the interplay between the parameters of the system, and their collective role in determining the performance of the swimmer can be readily observed and understood. In particular, the reduced model is applied to understand how wave amplitude, wave speed, and St must relate for optimal swimming efficiency. Following this, we then explore how these relationships are altered by geometric factors such as tail size and compliance.

  11. Swimming and other activities: applied aspects of fish swimming performance

    USGS Publications Warehouse

    Castro-Santos, Theodore R.; Farrell, A.P.

    2011-01-01

    Human activities such as hydropower development, water withdrawals, and commercial fisheries often put fish species at risk. Engineered solutions designed to protect species or their life stages are frequently based on assumptions about swimming performance and behaviors. In many cases, however, the appropriate data to support these designs are either unavailable or misapplied. This article provides an overview of the state of knowledge of fish swimming performance – where the data come from and how they are applied – identifying both gaps in knowledge and common errors in application, with guidance on how to avoid repeating mistakes, as well as suggestions for further study.

  12. Fish Swimming and Bird/Insect Flight

    NASA Astrophysics Data System (ADS)

    Wu, Theodore Yaotsu

    2011-01-01

    This expository review is devoted to fish swimming and bird/insect flight. (a) The simple waving motion of an elongated flexible ribbon plate of constant width propagating a wave distally down the plate to swim forward in a fluid, initially at rest, is first considered to provide a fundamental concept on energy conservation. It is generalized to include variations in body width and thickness, with appended dorsal, ventral and caudal fins shedding vortices to closely simulate fish swimming, for which a nonlinear theory is presented for large-amplitude propulsion. (b) For bird flight, the pioneering studies on oscillatory rigid wings are discussed with delineating a fully nonlinear unsteady theory for a two-dimensional flexible wing with arbitrary variations in shape and trajectory to provide a comparative study with experiments. (c) For insect flight, recent advances are reviewed by items on aerodynamic theory and modeling, computational methods, and experiments, for forward and hovering flights with producing leading-edge vortex to yield unsteady high lift. (d) Prospects are explored on extracting prevailing intrinsic flow energy by fish and bird to enhance thrust for propulsion. (e) The mechanical and biological principles are drawn together for unified studies on the energetics in deriving metabolic power for animal locomotion, leading to the surprising discovery that the hydrodynamic viscous drag on swimming fish is largely associated with laminar boundary layers, thus drawing valid and sound evidences for a resounding resolution to the long-standing fish-swim paradox proclaimed by Gray (1936, 1968 ).

  13. Swimming in air-breathing fishes.

    PubMed

    Lefevre, S; Domenici, P; McKenzie, D J

    2014-03-01

    Fishes with bimodal respiration differ in the extent of their reliance on air breathing to support aerobic metabolism, which is reflected in their lifestyles and ecologies. Many freshwater species undertake seasonal and reproductive migrations that presumably involve sustained aerobic exercise. In the six species studied to date, aerobic exercise in swim flumes stimulated air-breathing behaviour, and there is evidence that surfacing frequency and oxygen uptake from air show an exponential increase with increasing swimming speed. In some species, this was associated with an increase in the proportion of aerobic metabolism met by aerial respiration, while in others the proportion remained relatively constant. The ecological significance of anaerobic swimming activities, such as sprinting and fast-start manoeuvres during predator-prey interactions, has been little studied in air-breathing fishes. Some species practise air breathing during recovery itself, while others prefer to increase aquatic respiration, possibly to promote branchial ion exchange to restore acid-base balance, and to remain quiescent and avoid being visible to predators. Overall, the diversity of air-breathing fishes is reflected in their swimming physiology as well, and further research is needed to increase the understanding of the differences and the mechanisms through which air breathing is controlled and used during exercise.

  14. On the efficiency of fish like swimming

    NASA Astrophysics Data System (ADS)

    Bergmann, Michel; Iollo, Angelo; Inria Team Mc2 Team

    2012-11-01

    The aim of this talk is to present a parametric study of underwater locomotion via numerical simulations. The Navier-Stokes equations are discretized onto a cartesian mesh and the interface between the fluid and the fish is computed using an immersed boundary method. The lagrangian motion of the swimmer is computed from the Newton's laws. We present results showing how the swimming efficiency is influenced by the reynolds number and the swimming law. This work has been supported by French National Research Agency (ANR) through COSINUS program (project CARPEINTER no. ANR-08-COSI-002).

  15. Hydrokinetic Turbine Effects on Fish Swimming Behaviour

    PubMed Central

    Hammar, Linus; Andersson, Sandra; Eggertsen, Linda; Haglund, Johan; Gullström, Martin; Ehnberg, Jimmy; Molander, Sverker

    2013-01-01

    Hydrokinetic turbines, targeting the kinetic energy of fast-flowing currents, are under development with some turbines already deployed at ocean sites around the world. It remains virtually unknown as to how these technologies affect fish, and rotor collisions have been postulated as a major concern. In this study the effects of a vertical axis hydrokinetic rotor with rotational speeds up to 70 rpm were tested on the swimming patterns of naturally occurring fish in a subtropical tidal channel. Fish movements were recorded with and without the rotor in place. Results showed that no fish collided with the rotor and only a few specimens passed through rotor blades. Overall, fish reduced their movements through the area when the rotor was present. This deterrent effect on fish increased with current speed. Fish that passed the rotor avoided the near-field, about 0.3 m from the rotor for benthic reef fish. Large predatory fish were particularly cautious of the rotor and never moved closer than 1.7 m in current speeds above 0.6 ms-1. The effects of the rotor differed among taxa and feeding guilds and it is suggested that fish boldness and body shape influenced responses. In conclusion, the tested hydrokinetic turbine rotor proved non-hazardous to fish during the investigated conditions. However, the results indicate that arrays comprising multiple turbines may restrict fish movements, particularly for large species, with possible effects on habitat connectivity if migration routes are exploited. Arrays of the investigated turbine type and comparable systems should therefore be designed with gaps of several metres width to allow large fish to pass through. In combination with further research the insights from this study can be used for guiding the design of hydrokinetic turbine arrays where needed, so preventing ecological impacts. PMID:24358334

  16. Hydrokinetic turbine effects on fish swimming behaviour.

    PubMed

    Hammar, Linus; Andersson, Sandra; Eggertsen, Linda; Haglund, Johan; Gullström, Martin; Ehnberg, Jimmy; Molander, Sverker

    2013-01-01

    Hydrokinetic turbines, targeting the kinetic energy of fast-flowing currents, are under development with some turbines already deployed at ocean sites around the world. It remains virtually unknown as to how these technologies affect fish, and rotor collisions have been postulated as a major concern. In this study the effects of a vertical axis hydrokinetic rotor with rotational speeds up to 70 rpm were tested on the swimming patterns of naturally occurring fish in a subtropical tidal channel. Fish movements were recorded with and without the rotor in place. Results showed that no fish collided with the rotor and only a few specimens passed through rotor blades. Overall, fish reduced their movements through the area when the rotor was present. This deterrent effect on fish increased with current speed. Fish that passed the rotor avoided the near-field, about 0.3 m from the rotor for benthic reef fish. Large predatory fish were particularly cautious of the rotor and never moved closer than 1.7 m in current speeds above 0.6 ms(-1). The effects of the rotor differed among taxa and feeding guilds and it is suggested that fish boldness and body shape influenced responses. In conclusion, the tested hydrokinetic turbine rotor proved non-hazardous to fish during the investigated conditions. However, the results indicate that arrays comprising multiple turbines may restrict fish movements, particularly for large species, with possible effects on habitat connectivity if migration routes are exploited. Arrays of the investigated turbine type and comparable systems should therefore be designed with gaps of several metres width to allow large fish to pass through. In combination with further research the insights from this study can be used for guiding the design of hydrokinetic turbine arrays where needed, so preventing ecological impacts.

  17. Locomotor forces on a swimming fish: three-dimensional vortex wake dynamics quantified using digital particle image velocimetry.

    PubMed

    Drucker; Lauder

    1999-01-01

    Quantifying the locomotor forces experienced by swimming fishes represents a significant challenge because direct measurements of force applied to the aquatic medium are not feasible. However, using the technique of digital particle image velocimetry (DPIV), it is possible to quantify the effect of fish fins on water movement and hence to estimate momentum transfer from the animal to the fluid. We used DPIV to visualize water flow in the wake of the pectoral fins of bluegill sunfish (Lepomis macrochirus) swimming at speeds of 0.5-1.5 L s(-)(1), where L is total body length. Velocity fields quantified in three perpendicular planes in the wake of the fins allowed three-dimensional reconstruction of downstream vortex structures. At low swimming speed (0.5 L s(-)(1)), vorticity is shed by each fin during the downstroke and stroke reversal to generate discrete, roughly symmetrical, vortex rings of near-uniform circulation with a central jet of high-velocity flow. At and above the maximum sustainable labriform swimming speed of 1.0 L s(-)(1), additional vorticity appears on the upstroke, indicating the production of linked pairs of rings by each fin. Fluid velocity measured in the vicinity of the fin indicates that substantial spanwise flow during the downstroke may occur as vortex rings are formed. The forces exerted by the fins on the water in three dimensions were calculated from vortex ring orientation and momentum. Mean wake-derived thrust (11.1 mN) and lift (3.2 mN) forces produced by both fins per stride at 0.5 L s(-)(1) were found to match closely empirically determined counter-forces of body drag and weight. Medially directed reaction forces were unexpectedly large, averaging 125 % of the thrust force for each fin. Such large inward forces and a deep body that isolates left- and right-side vortex rings are predicted to aid maneuverability. The observed force balance indicates that DPIV can be used to measure accurately large-scale vorticity in the wake of

  18. Towards direct numerical simulation of freely swimming fish.

    NASA Astrophysics Data System (ADS)

    Curet, Oscar; Patankar, Neelesh; Maciver, Malcolm

    2006-11-01

    Swimming mechanisms employed by fish are currently inspiring unique underwater vehicles and robotic devices as well as basic science research into the neural control of movement. Key engineering issues include propulsion efficiency, precise motion control and maneuverability. A numerical scheme that simulates the motion of freely swimming fish will be a valuable design and research tool. We are working towards this goal. In particular we are interested in simulating the motion of a gymnotiform fish that swims by producing undulations of a ventral ribbon fin while keeping its body rigid. We model the fish as a rigid body with an attached undulating membrane. In our numerical scheme the key idea is to assume that the entire fluid-fish domain is a fluid. Then we impose two constraints: the first requires that the fluid in the region occupied by the fish body moves rigidly (a fictitious domain approach), and the second requires that the fluid at the location of the fin has the traveling wave velocity of the fin (an immersed boundary approach). Given the traveling wave form of the fin, the objective is for the numerical scheme to give the swimming velocity of the fish by solving the coupled fluid-fish problem. We will present results for the forces generated by a fin attached to a fixed body and preliminary results for freely swimming fish.

  19. Swimming efficiency and the influence of morphology on swimming costs in fishes.

    PubMed

    Ohlberger, J; Staaks, G; Hölker, F

    2006-01-01

    Swimming performance is considered a main character determining survival in many aquatic animals. Body morphology highly influences the energetic costs and efficiency of swimming and sets general limits on a species capacity to use habitats and foods. For two cyprinid fishes with different morphological characteristics, carp (Cyprinus carpio L.) and roach (Rutilus rutilus (L.)), optimum swimming speeds (U(mc)) as well as total and net costs of transport (COT, NCOT) were determined to evaluate differences in their swimming efficiency. Costs of transport and optimum speeds proved to be allometric functions of fish mass. NCOT was higher but U(mc) was lower in carp, indicating a lower swimming efficiency compared to roach. The differences in swimming costs are attributed to the different ecological demands of the species and could partly be explained by their morphological characteristics. Body fineness ratios were used to quantify the influence of body shape on activity costs. This factor proved to be significantly different between the species, indicating a better streamlining in roach with values closer to the optimum body form for efficient swimming. Net swimming costs were directly related to fish morphology.

  20. Ectoparasites increase swimming costs in a coral reef fish.

    PubMed

    Binning, Sandra A; Roche, Dominique G; Layton, Cayne

    2013-02-23

    Ectoparasites can reduce individual fitness by negatively affecting behavioural, morphological and physiological traits. In fishes, there are potential costs if ectoparasites decrease streamlining, thereby directly compromising swimming performance. Few studies have examined the effects of ectoparasites on fish swimming performance and none distinguish between energetic costs imposed by changes in streamlining and effects on host physiology. The bridled monocle bream (Scolopsis bilineatus) is parasitized by an isopod (Anilocra nemipteri), which attaches above the eye. We show that parasitized fish have higher standard metabolic rates (SMRs), poorer aerobic capacities and lower maximum swimming speeds than non-parasitized fish. Adding a model parasite did not affect SMR, but reduced maximum swimming speed and elevated oxygen consumption rates at high speeds to levels observed in naturally parasitized fish. This demonstrates that ectoparasites create drag effects that are important at high speeds. The higher SMR of naturally parasitized fish does, however, reveal an effect of parasitism on host physiology. This effect was easily reversed: fish whose parasite was removed 24 h earlier did not differ from unparasitized fish in any performance metrics. In sum, the main cost of this ectoparasite is probably its direct effect on streamlining, reducing swimming performance at high speeds.

  1. Ectoparasites increase swimming costs in a coral reef fish

    PubMed Central

    Binning, Sandra A.; Roche, Dominique G.; Layton, Cayne

    2013-01-01

    Ectoparasites can reduce individual fitness by negatively affecting behavioural, morphological and physiological traits. In fishes, there are potential costs if ectoparasites decrease streamlining, thereby directly compromising swimming performance. Few studies have examined the effects of ectoparasites on fish swimming performance and none distinguish between energetic costs imposed by changes in streamlining and effects on host physiology. The bridled monocle bream (Scolopsis bilineatus) is parasitized by an isopod (Anilocra nemipteri), which attaches above the eye. We show that parasitized fish have higher standard metabolic rates (SMRs), poorer aerobic capacities and lower maximum swimming speeds than non-parasitized fish. Adding a model parasite did not affect SMR, but reduced maximum swimming speed and elevated oxygen consumption rates at high speeds to levels observed in naturally parasitized fish. This demonstrates that ectoparasites create drag effects that are important at high speeds. The higher SMR of naturally parasitized fish does, however, reveal an effect of parasitism on host physiology. This effect was easily reversed: fish whose parasite was removed 24 h earlier did not differ from unparasitized fish in any performance metrics. In sum, the main cost of this ectoparasite is probably its direct effect on streamlining, reducing swimming performance at high speeds. PMID:23193046

  2. Flow Structures and Efficiency of Swimming Fish school: Numerical Study

    NASA Astrophysics Data System (ADS)

    Yatagai, Yuzuru; Hattori, Yuji

    2013-11-01

    The flow structure and energy-saving mechanism in fish school is numerically investigated by using the volume penalization method. We calculate the various patterns of configuration of fishes and investigate the relation between spatial arrangement and the performance of fish. It is found that the down-stream fish gains a hydrodynamic advantage from the upstream wake shed by the upstream fish. The most efficient configuration is that the downstream fish is placed in the wake. It reduces the drag force of the downstream fish in comparison with that in solo swimming.

  3. Locomotion Performance of Biomimetic Fish-like Swimming Devices

    NASA Astrophysics Data System (ADS)

    Epps, Brenden P.; Valdivia Y Alvarado, Pablo; Techet, Alexandra H.

    2007-11-01

    The swimming performance of a biomimetic, fish-like swimming device, designed to exploit the natural dynamics of its compliant body to achieve locomotion, is studied experimentally. A theoretical model combines beam-bending stress analysis and unsteady hydrodynamic forcing with known material properties of the robot to reveal desired geometry distributions and actuation modes. Swimming kinematics and corresponding performance of the device are also predicted and tested for a carangiform prototype device in a quiescent tank of water. Experimental swimming tests show good agreement with the simplified theoretical models. The hydrodynamic characteristics of the wake behind the device are investigated using time-resolved particle imaging velocimetry (PIV) over a range of tail beat frequencies, from 1 to 4 Hz, to asses vortical wake patterns and hydrodynamic forces. PIV data are compared to theoretical model predictions. Reynolds numbers for the swimming device are between 2500 and 8500 based on body length.

  4. Swimming performance of a biomimetic compliant fish-like robot

    NASA Astrophysics Data System (ADS)

    Epps, Brenden P.; Valdivia Y Alvarado, Pablo; Youcef-Toumi, Kamal; Techet, Alexandra H.

    2009-12-01

    Digital particle image velocimetry and fluorescent dye visualization are used to characterize the performance of fish-like swimming robots. During nominal swimming, these robots produce a ‘V’-shaped double wake, with two reverse-Kármán streets in the far wake. The Reynolds number based on swimming speed and body length is approximately 7500, and the Strouhal number based on flapping frequency, flapping amplitude, and swimming speed is 0.86. It is found that swimming speed scales with the strength and geometry of a composite wake, which is constructed by freezing each vortex at the location of its centroid at the time of shedding. Specifically, we find that swimming speed scales linearly with vortex circulation. Also, swimming speed scales linearly with flapping frequency and the width of the composite wake. The thrust produced by the swimming robot is estimated using a simple vortex dynamics model, and we find satisfactory agreement between this estimate and measurements made during static load tests.

  5. Impulse generated during unsteady maneuvering of swimming fish

    NASA Astrophysics Data System (ADS)

    Epps, Brenden P.; Techet, Alexandra H.

    2007-11-01

    The relationship between the maneuvering kinematics of a Giant Danio ( Danio aequipinnatus) and the resulting vortical wake is investigated for a rapid, ‘C’-start maneuver using fully time-resolved (500 Hz) particle image velocimetry (PIV). PIV illuminates the two distinct vortices formed during the turn. The fish body rotation is facilitated by the initial, or “maneuvering” vortex formation, and the final fish velocity is augmented by the strength of the second, “propulsive” vortex. Results confirm that the axisymmetric vortex ring model is reasonable to use in calculating the hydrodynamic impulse acting on the fish. The total linear momentum change of the fish from its initial swimming trajectory to its final swimming trajectory is balanced by the vector sum of the impulses of both vortex rings. The timing of vortex formation is uniquely synchronized with the fish motion, and the choreography of the maneuver is addressed in the context of the resulting hydrodynamic forces.

  6. Impulse generated during unsteady maneuvering of swimming fish

    NASA Astrophysics Data System (ADS)

    Epps, Brenden P.; Techet, Alexandra H.

    The relationship between the maneuvering kinematics of a Giant Danio (Danio aequipinnatus) and the resulting vortical wake is investigated for a rapid, 'C'-start maneuver using fully time-resolved (500 Hz) particle image velocimetry (PIV). PIV illuminates the two distinct vortices formed during the turn. The fish body rotation is facilitated by the initial, or "maneuvering" vortex formation, and the final fish velocity is augmented by the strength of the second, "propulsive" vortex. Results confirm that the axisymmetric vortex ring model is reasonable to use in calculating the hydrodynamic impulse acting on the fish. The total linear momentum change of the fish from its initial swimming trajectory to its final swimming trajectory is balanced by the vector sum of the impulses of both vortex rings. The timing of vortex formation is uniquely synchronized with the fish motion, and the choreography of the maneuver is addressed in the context of the resulting hydrodynamic forces.

  7. Analytical insights into optimality and resonance in fish swimming

    PubMed Central

    Kohannim, Saba; Iwasaki, Tetsuya

    2014-01-01

    This paper provides analytical insights into the hypothesis that fish exploit resonance to reduce the mechanical cost of swimming. A simple body–fluid fish model, representing carangiform locomotion, is developed. Steady swimming at various speeds is analysed using optimal gait theory by minimizing bending moment over tail movements and stiffness, and the results are shown to match with data from observed swimming. Our analysis indicates the following: thrust–drag balance leads to the Strouhal number being predetermined based on the drag coefficient and the ratio of wetted body area to cross-sectional area of accelerated fluid. Muscle tension is reduced when undulation frequency matches resonance frequency, which maximizes the ratio of tail-tip velocity to bending moment. Finally, hydrodynamic resonance determines tail-beat frequency, whereas muscle stiffness is actively adjusted, so that overall body–fluid resonance is exploited. PMID:24430125

  8. Analytical insights into optimality and resonance in fish swimming.

    PubMed

    Kohannim, Saba; Iwasaki, Tetsuya

    2014-03-06

    This paper provides analytical insights into the hypothesis that fish exploit resonance to reduce the mechanical cost of swimming. A simple body-fluid fish model, representing carangiform locomotion, is developed. Steady swimming at various speeds is analysed using optimal gait theory by minimizing bending moment over tail movements and stiffness, and the results are shown to match with data from observed swimming. Our analysis indicates the following: thrust-drag balance leads to the Strouhal number being predetermined based on the drag coefficient and the ratio of wetted body area to cross-sectional area of accelerated fluid. Muscle tension is reduced when undulation frequency matches resonance frequency, which maximizes the ratio of tail-tip velocity to bending moment. Finally, hydrodynamic resonance determines tail-beat frequency, whereas muscle stiffness is actively adjusted, so that overall body-fluid resonance is exploited.

  9. "Spilling Over": Fish Swimming Kinematics in Cylinder Wakes

    NASA Astrophysics Data System (ADS)

    Wilson, C. A.; Muhawenimana, V.; Cable, J.

    2016-12-01

    Our understanding of fish swimming kinematics and behaviour in turbulent altered and pseudo-natural flows remains incomplete. This study aims to examine velocity, turbulence and wake metrics that govern fish stability and other behavioural traits in the turbulent wake of a horizontal cylinder. In a free surface flume, the swimming behaviour of Nile tilapia (Oreochromis niloticus, Silver strain) was monitored over a range of cylinder diameter (D) Reynolds numbers from 2.8 x103 to 25.8 x103. Spills, defined as loss of both balance and posture, were inversely correlated with fish length and weight; where smaller fish in the 50th percentile of standard length, lost balance more often and accounted for 65% of the total number (533) of spills. Additionally, the bigger fish in the 95th percentile, experienced <0.5% of all recorded spills. Such findings are in keeping with a previous study where the spill occurrence increased with decreasing fish length to eddy size ratio. Fish spent the majority of station holding time within a two diameter (2D) distance closest to the flume bed and in a downstream distance of 3D to 6D from the cylinder. The frequency of occurrence of spills increased with increasing Reynolds number for the whole fish population until an intermediate Reynolds number of 11.5 x103 was reached, where the frequency in spills steadily declined with increasing Reynolds number until the end of the test duration. The spill frequency-Reynolds number relationship indicates a shift in cylinder wake dynamics. Further analysis of the measured velocity statistics will help determine the intensity, periodicity and the turbulence length scale of the wake structure and their correlations with the observed fish swimming kinematics.

  10. Simulations of the burst and coast swimming behavior of fish

    NASA Astrophysics Data System (ADS)

    Zhou, Quan; Moored, Keith; Smits, Alexander

    2013-11-01

    An investigation into the burst and coast swimming behavior of fish is simulated with a 2-D, inviscid Boundary Element Method. The fish is modeled as a thin pitching panel that is allowed to free swim. A simple drag model is used where drag is proportional to the velocity squared in order to calculate the cruising velocity. The burst-coast behavior is modeled by a coasting phase, where the panel is motionless, and a burst phase, where the panel pitches with a single sine wave motion. Varying the frequency of the fin-beat and the duration of the duty cycle (the ratio of the burst-phase to the entire period), it is found that it is possible to alter swimming motion to yield a decrease of 50% in the cost of transport with no sacrifice of time-averaged cruising velocity. The analyses of the wake structure demonstrate how vortices shed by the fish affect and shape swimming dynamics. Supported by the Office of Naval Research under Program Director Dr. Bob Brizzolara, MURI grant number N00014-08-1-0642.

  11. Effects of altered gravity on the swimming behaviour of fish

    NASA Astrophysics Data System (ADS)

    Hilbig, R.; Anken, R. H.; Sonntag, G.; Höhne, S.; Henneberg, J.; Kretschmer, N.; Rahmann, H.

    Humans taking part in parabolic aircraft flights (PAFs) may suffer from space motion sickness-phenomena (SMS, a kinetosis). It has been argued that SMS during PAFs might not be based on microgravity alone but rather on changing accelerations from 0g to 2g. We test here the hypothesis that PAF-induced kinetosis is based on asymmetric statoliths (i.e., differently weighed statoliths on the right and the left side of the head), with asymmetric inputs to the brain being disclosed at microgravity. Since fish frequently reveal kinetotic behaviour during PAFs (especially so-called spinning movements and looping responses), we investigated (1) whether or not kinetotically swimming fish at microgravity would have a pronounced inner ear otolith asymmetry and (2) whether or not slow translational and continuously changing linear (vertical) acceleration on ground induced kinetosis. These latter accelerations were applied using a specially developed parabel-animal-container (PAC) to stimulate the cupular organs. The results suggest that the fish tested on ground can counter changing accelerations successfully without revealing kinetotic swimming patterns. Kinetosis could only be induced by PAFs. This finding suggests that it is indeed microgravity rather than changing accelerations, which induces kinetosis. Moreover, we demonstrate that fish swimming kinetotically during PAFs correlates with a higher otolith asymmetry in comparison to normally behaving animals in PAFs.

  12. Three-dimensional spatial representation in freely swimming fish.

    PubMed

    Burt de Perera, Theresa; Holbrook, Robert I

    2012-08-01

    Research on spatial cognition has focused on how animals encode the horizontal component of space. However, most animals travel vertically within their environments, particularly those that fly or swim. Pelagic fish move with six degrees of freedom and must integrate these components to navigate accurately--how do they do this? Using an assay based on associative learning of the vertical and horizontal components of space within a rotating Y-maze, we found that fish (Astyanax fasciatus) learned and remembered information from both horizontal and vertical axes when they were presented either separately or as an integrated three-dimensional unit. When information from the two components conflicted, the fish used the previously learned vertical information in preference to the horizontal. This not only demonstrates that the horizontal and vertical components are stored separately in the fishes' representation of space (simplifying the problem of 3D navigation), but also suggests that the vertical axis contains particularly salient spatial cues--presumably including hydrostatic pressure. To explore this latter possibility, we developed a physical theoretical model that shows how fish could determine their absolute depth using pressure. We next considered full volumetric spatial cognition. Astyanax were trained to swim towards a reward in a Y-maze that could be rotated, before the arms were removed during probe trials. The subjects were tracked in three dimensions as they swam freely through the surrounding cubic tank. The results revealed that fish are able to accurately encode metric information in a volume, and that the error accrued in the horizontal and vertical axes whilst swimming in probe trials was similar. Together, these experiments demonstrate that unlike in surface-bound rats, the vertical component of the representation of space is vitally important to fishes. We hypothesise that the representation of space in the brain of vertebrates could ultimately be

  13. Modeling and simulation of fish swimming with active muscles.

    PubMed

    Curatolo, Michele; Teresi, Luciano

    2016-11-21

    Our goal is to reproduce the key features of carangiform swimming by modeling muscle functioning using the notion of active distortions, thus emphasizing the kinematical role of muscle, the generation of movement, rather than the dynamical one, the production of force. This approach, already proposed to model the action of muscles in different contexts, is here tested again for the problem of developing an effective and reliable framework to model and simulate swimming. A proper undulatory movement of a fish-like body is reproduced by defining a pattern of distortions, tuned in both space and time, meant to model the muscles activation which produce the flexural motion of body fish; eventually, interactions with the surrounding water yields the desired thrust. Carangiform swimmers have a relatively inflexible anterior body section and a generally flat, flexible posterior section. Because of this configuration, undulations sent rearward along the body attain a significant amplitude only in the posterior section. We compare the performances of different swimming gaits, and we are able to find some important relations between key parameters such as frequencies, wavelength, tail amplitude, and the achieved swim velocity, or the generated thrust, which summarize the swimming performance. In particular, an interesting relation is found between the Strouhal number and the wavelength of muscles activation. We highlight the muscle function during fish locomotion describing the activation of muscles and the relation between the force production and the shortening-lengthening cycle of muscle. We found a great accordance between results and empirical relations, giving an implicit validation of our models. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. Evolutionarily Stable Strategies for Fecundity and Swimming Speed of Fish.

    PubMed

    Plank, Michael J; Pitchford, Jonathan W; James, Alex

    2016-02-01

    Many pelagic fish species have a life history that involves producing a large number of small eggs. This is the result of a trade-off between fecundity and larval survival probability. There are also trade-offs involving other traits, such as larval swimming speed. Swimming faster increases the average food encounter rate but also increases the metabolic cost. Here we introduce an evolutionary model comprising fecundity and swimming speed as heritable traits. We show that there can be two evolutionary stable strategies. In environments where there is little noise in the food encounter rate, the stable strategy is a low-fecundity strategy with a swimming speed that minimises the mean time taken to reach reproductive maturity. However, in noisy environments, for example where the prey distribution is patchy or the water is turbulent, strategies that optimise mean outcomes are often outperformed by strategies that increase inter-individual variance. We show that, when larval growth rates are unpredictable, a high-fecundity strategy is evolutionarily stable. In a population following this strategy, the swimming speed is higher than would be anticipated by maximising the mean growth rate.

  15. Modeling the effect of varying swim speeds on fish passage through velocity barriers

    USGS Publications Warehouse

    Castro-Santos, T.

    2006-01-01

    The distance fish can swim through zones of high-velocity flow is an important factor limiting the distribution and conservation of riverine and diadromous fishes. Often, these barriers are characterized by nonuniform flow conditions, and it is likely that fish will swim at varying speeds to traverse them. Existing models used to predict passage success, however, typically include the unrealistic assumption that fish swim at a constant speed regardless of the speed of flow. This paper demonstrates how the maximum distance of ascent through velocity barriers can be estimated from the swim speed-fatigue time relationship, allowing for variation in both swim speed and water velocity.

  16. Optimum swimming pathways of fish spawning migrations in rivers

    USGS Publications Warehouse

    McElroy, Brandon; DeLonay, Aaron; Jacobson, Robert

    2012-01-01

    Fishes that swim upstream in rivers to spawn must navigate complex fluvial velocity fields to arrive at their ultimate locations. One hypothesis with substantial implications is that fish traverse pathways that minimize their energy expenditure during migration. Here we present the methodological and theoretical developments necessary to test this and similar hypotheses. First, a cost function is derived for upstream migration that relates work done by a fish to swimming drag. The energetic cost scales with the cube of a fish's relative velocity integrated along its path. By normalizing to the energy requirements of holding a position in the slowest waters at the path's origin, a cost function is derived that depends only on the physical environment and not on specifics of individual fish. Then, as an example, we demonstrate the analysis of a migration pathway of a telemetrically tracked pallid sturgeon (Scaphirhynchus albus) in the Missouri River (USA). The actual pathway cost is lower than 105 random paths through the surveyed reach and is consistent with the optimization hypothesis. The implication—subject to more extensive validation—is that reproductive success in managed rivers could be increased through manipulation of reservoir releases or channel morphology to increase abundance of lower-cost migration pathways.

  17. Optimum swimming pathways of fish spawning migrations in rivers

    USGS Publications Warehouse

    McElroy, Brandon; DeLonay, Aaron; Jacobson, Robert

    2012-01-01

    Fishes that swim upstream in rivers to spawn must navigate complex fluvial velocity fields to arrive at their ultimate locations. One hypothesis with substantial implications is that fish traverse pathways that minimize their energy expenditure during migration. Here we present the methodological and theoretical developments necessary to test this and similar hypotheses. First, a cost function is derived for upstream migration that relates work done by a fish to swimming drag. The energetic cost scales with the cube of a fish's relative velocity integrated along its path. By normalizing to the energy requirements of holding a position in the slowest waters at the path's origin, a cost function is derived that depends only on the physical environment and not on specifics of individual fish. Then, as an example, we demonstrate the analysis of a migration pathway of a telemetrically tracked pallid sturgeon (Scaphirhynchus albus) in the Missouri River (USA). The actual pathway cost is lower than 105 random paths through the surveyed reach and is consistent with the optimization hypothesis. The implication—subject to more extensive validation—is that reproductive success in managed rivers could be increased through manipulation of reservoir releases or channel morphology to increase abundance of lower-cost migration pathways.

  18. The effects of steady swimming on fish escape performance.

    PubMed

    Anwar, Sanam B; Cathcart, Kelsey; Darakananda, Karin; Gaing, Ashley N; Shin, Seo Yim; Vronay, Xena; Wright, Dania N; Ellerby, David J

    2016-06-01

    Escape maneuvers are essential to the survival and fitness of many animals. Escapes are frequently initiated when an animal is already in motion. This may introduce constraints that alter the escape performance. In fish, escape maneuvers and steady, body caudal fin (BCF) swimming are driven by distinct patterns of curvature of the body axis. Pre-existing muscle activity may therefore delay or diminish a response. To quantify the performance consequences of escaping in flow, escape behavior was examined in bluegill sunfish (Lepomis macrochirus) in both still-water and during steady swimming. Escapes executed during swimming were kinematically less variable than those made in still-water. Swimming escapes also had increased response latencies and lower peak velocities and accelerations than those made in still-water. Performance was also lower for escapes made up rather than down-stream, and a preference for down-stream escapes may be associated with maximizing performance. The constraints imposed by pre-existing motion and flow, therefore, have the potential to shape predator-prey interactions under field conditions by shifting the optimal strategies for both predators and prey.

  19. Stability versus Maneuvering: Challenges for Stability during Swimming by Fishes.

    PubMed

    Webb, Paul W; Weihs, Daniel

    2015-10-01

    Fishes are well known for their remarkable maneuverability and agility. Less visible is the continuous control of stability essential for the exploitation of the full range of aquatic resources. Perturbations to posture and trajectory arise from hydrostatic and hydrodynamic forces centered in a fish (intrinsic) and from the environment (extrinsic). Hydrostatic instabilities arise from vertical and horizontal separation of the centers of mass (CM) and of buoyancy, thereby creating perturbations in roll, yaw, and pitch, with largely neglected implications for behavioral ecology. Among various forms of hydrodynamic stability, the need for stability in the face of recoil forces from propulsors is close to universal. Destabilizing torques in body-caudal fin swimming is created by inertial and viscous forces through a propulsor beat. The recoil component is reduced, damped, and corrected in various ways, including kinematics, shape of the body and fins, and deployment of the fins. We postulate that control of the angle of orientation, θ, of the trailing edge is especially important in the evolution and lifestyles of fishes, but studies are few. Control of stability and maneuvering are reflected in accelerations around the CM. Accelerations for such motions may give insight into time-behavior patterns in the wild but cannot be used to determine the expenditure of energy by free-swimming fishes.

  20. Metabolic fuel kinetics in fish: swimming, hypoxia and muscle membranes.

    PubMed

    Weber, Jean-Michel; Choi, Kevin; Gonzalez, Alex; Omlin, Teye

    2016-01-01

    Muscle performance depends on the supply of metabolic fuels and disposal of end-products. Using circulating metabolite concentrations to infer changes in fluxes is highly unreliable because the relationship between these parameters varies greatly with physiological state. Quantifying fuel kinetics directly is therefore crucial to the understanding of muscle metabolism. This review focuses on how carbohydrates, lipids and amino acids are provided to fish muscles during hypoxia and swimming. Both stresses force white muscle to produce lactate at higher rates than it can be processed by aerobic tissues. However, lactate accumulation is minimized because disposal is also strongly stimulated. Exogenous supply shows that trout have a much higher capacity to metabolize lactate than observed during hypoxia or intense swimming. The low density of monocarboxylate transporters and their lack of upregulation with exercise explain the phenomenon of white muscle lactate retention. This tissue operates as a quasi-closed system, where glycogen stores act as an 'energy spring' that alternates between explosive power release during swimming and slow recoil from lactate in situ during recovery. To cope with exogenous glucose, trout can completely suppress hepatic production and boost glucose disposal. Without these responses, glycemia would increase four times faster and reach dangerous levels. The capacity of salmonids for glucoregulation is therefore much better than presently described in the literature. Instead of albumin-bound fatty acids, fish use lipoproteins to shuttle energy from adipose tissue to working muscles during prolonged exercise. Proteins may play an important role in fueling muscle work in fish, but their exact contribution is yet to be established. The membrane pacemaker theory of metabolism accurately predicts general properties of muscle membranes such as unsaturation, but it does not explain allometric patterns of specific fatty acids. Investigations of

  1. Swimming behavior of larval Medaka fish under microgravity

    NASA Astrophysics Data System (ADS)

    Furukawa, R.; Ijiri, K.

    Fish exhibit looping and rolling behaviors when subjected to short periods of microgravity during parabolic flight. Strain-differences in the behavioral response of adult Medaka fish ( Oryzias latipes) were reported previously, however, there have been few studies of larval fish behavior under microgravity. In the present study, we investigated whether microgravity affects the swimming behavior of larvae at various ages (0 to 20 days after hatching), using different strains: HNI-II, HO5, ha strain, and variety of different strains (variety). The preliminary experiments were done in the ground laboratory: the development of eyesight was examined using optokinetic response for the different strains. The visual acuity of larvae improved drastically during 20 days after hatching. Strain differences of response were noted for the development of their visual acuity. In microgravity, the results were significantly different from those of adult Medaka. The larval fish appeared to maintain their orientation, except that a few of them exhibited looping and rolling behavior. Further, most larvae swam normally with their backs turning toward the light source (dorsal light response, DLR), and the rest of them stayed with their abdomen touching the surface of the container (ventral substrate response, VSR). For larval stages, strain-differences and age-differences in behavior were observed, but less pronounced than with adult fish under microgravity. Our observations suggest that adaptability of larval fish to the gravitational change and the mechanism of their postural control in microgravity are more variable than in adult fish.

  2. Fish swimming in schools save energy regardless of their spatial position.

    PubMed

    Marras, Stefano; Killen, Shaun S; Lindström, Jan; McKenzie, David J; Steffensen, John F; Domenici, Paolo

    For animals, being a member of a group provides various advantages, such as reduced vulnerability to predators, increased foraging opportunities and reduced energetic costs of locomotion. In moving groups such as fish schools, there are benefits of group membership for trailing individuals, who can reduce the cost of movement by exploiting the flow patterns generated by the individuals swimming ahead of them. However, whether positions relative to the closest neighbours (e.g. ahead, sided by side or behind) modulate the individual energetic cost of swimming is still unknown. Here, we addressed these questions in grey mullet Liza aurata by measuring tail-beat frequency and amplitude of 15 focal fish, swimming in separate schools, while swimming in isolation and in various positions relative to their closest neighbours, at three speeds. Our results demonstrate that, in a fish school, individuals in any position have reduced costs of swimming, compared to when they swim at the same speed but alone. Although fish swimming behind their neighbours save the most energy, even fish swimming ahead of their nearest neighbour were able to gain a net energetic benefit over swimming in isolation, including those swimming at the front of a school. Interestingly, this energetic saving was greatest at the lowest swimming speed measured in our study. Because any member of a school gains an energetic benefit compared to swimming alone, we suggest that the benefits of membership in moving groups may be more strongly linked to reducing the costs of locomotion than previously appreciated.

  3. 3D Synthetic Aperture PIV of a Freely Swimming Fish

    NASA Astrophysics Data System (ADS)

    Mendelson, Leah; Techet, Alexandra

    2012-11-01

    Fish owe much of their locomotive success to complex body geometries and wake interactions that cannot be fully characterized by planar experimental techniques including 2D PIV. Volumetric methods are valuable to illustrate and quantify these features, thus providing new insights for bioinspired design. In particular, synthetic aperture particle image velocimetry (SAPIV) uses light field imaging algorithms to reconstruct a 3D particle field which can then be analyzed using a 3D cross-correlation. Previous studies have shown that this technique is able to resolve all three velocity components on the same order length scale and to see around partial occlusions, such as a caudal fin, through the use of multiple cameras. To harness these capabilities for biomimetic use, SAPIV is used to depict the three-dimensional velocity field and vortical structures surrounding a freely swimming Giant danio (Devario aequipinnatus) during straight swims and turning maneuvers.

  4. Dimentionality and behavior of swimming Zebrafish: ``The EigenFish''

    NASA Astrophysics Data System (ADS)

    Girdhar, Kiran; Gruebele, Martin; Chemla, Yann

    2013-03-01

    How simple is the underlying control mechanism for the complex locomotion of vertebrates? To answer this question, we study the swimming behavior of zebrafish larvae. A dimensionality reduction method (singular value decomposition), in analogy to previous studies of worms, is used to analyze swimming movies of fish. That way, the animals can directly provide us with a minimal set of shapes to describe their motion, rather than us imposing arbitrary coordinates. We show that two low imensional attractors (an ellipse and a distorted ellipse) embedded in a threedimensional space of motion coordinates are sufficient to describe > 95% of the locomotion. We also show that scoots and R-turns, previously thought to be independent behaviors based on qualitative studies, are in fact just extremes of a continuous family of motions bounded by the two attractors.

  5. Vorticity Dynamics of Self-Propelled Swimming of 3D Bionic Fish

    NASA Astrophysics Data System (ADS)

    Xin, Z. Q.; Wu, C. J.

    2011-09-01

    Numerical simulations and control of tail-swaying swim of three-dimensional biomimetic fish in a viscous flow and the vorticity dynamics of fish swimming have been investigated in this paper, with a computational fluid dynamics package, which combines the adaptive multi-grid finite volume method and the methods of immersed boundary and volume of fluid, and the control strategy of fish motion. Using boundary vorticity-flux (BVF) theory, we have studied the mechanism of fish swimming and trace the physical root to the moving body surface. With the change of swimming speed, the effects of fish body and caudalfin on thrust, is analysed quantitatively. Finally the relationship between the forces exerted on fish body and vortex structures of fish swimming has been presented in this paper.

  6. Adjoint-based optimization of fish swimming gaits

    NASA Astrophysics Data System (ADS)

    Floryan, Daniel; Rowley, Clarence W.; Smits, Alexander J.

    2016-11-01

    We study a simplified model of fish swimming, namely a flat plate periodically pitching about its leading edge. Using gradient-based optimization, we seek periodic gaits that are optimal in regards to a particular objective (e.g. maximal thrust). The two-dimensional immersed boundary projection method is used to investigate the flow states, and its adjoint formulation is used to efficiently calculate the gradient of the objective function needed for optimization. The adjoint method also provides sensitivity information, which may be used to elucidate the physics responsible for optimality. Supported under ONR MURI Grants N00014-14-1-0533, Program Manager Bob Brizzolara.

  7. Modeling and simulation of fish-like swimming

    NASA Astrophysics Data System (ADS)

    Bergmann, M.; Iollo, A.

    2011-01-01

    Modeling and simulation of two-dimensional flows past deformable bodies are considered. The incompressible Navier-Stokes equations are discretized in space onto a fixed cartesian mesh and the displacement of deformable objects through the fluid is taken into account using a penalization method. The interface between the solid and the fluid is tracked using a level-set description so that it is possible to simulate several bodies freely evolving in the fluid. As an illustration of the methods, fish-like locomotion is analyzed in terms of propulsion efficiency. Underwater maneuvering and school swimming are also explored.

  8. Numerical simulations and vorticity dynamics of self-propelled swimming of 3D bionic fish

    NASA Astrophysics Data System (ADS)

    Xin, ZhiQiang; Wu, ChuiJie

    2012-02-01

    Numerical simulations and the control of self-propelled swimming of three-dimensional bionic fish in a viscous flow and the mechanism of fish swimming are carried out in this study, with a 3D computational fluid dynamics package, which includes the immersed boundary method and the volume of fluid method, the adaptive multi-grid finite volume method, and the control strategy of fish swimming. Firstly, the mechanism of 3D fish swimming was studied and the vorticity dynamics root was traced to the moving body surface by using the boundary vorticity-flux theory. With the change of swimming speed, the contributions of the fish body and caudal fin to thrust are analyzed quantitatively. The relationship between vortex structures of fish swimming and the forces exerted on the fish body are also given in this paper. Finally, the 3D wake structure of self-propelled swimming of 3D bionic fish is presented. The in-depth analysis of the 3D vortex structure in the role of 3D biomimetic fish swimming is also performed.

  9. Resolving Shifting Patterns of Muscle Energy Use in Swimming Fish

    PubMed Central

    Gerry, Shannon P.; Ellerby, David J.

    2014-01-01

    Muscle metabolism dominates the energy costs of locomotion. Although in vivo measures of muscle strain, activity and force can indicate mechanical function, similar muscle-level measures of energy use are challenging to obtain. Without this information locomotor systems are essentially a black box in terms of the distribution of metabolic energy. Although in situ measurements of muscle metabolism are not practical in multiple muscles, the rate of blood flow to skeletal muscle tissue can be used as a proxy for aerobic metabolism, allowing the cost of particular muscle functions to be estimated. Axial, undulatory swimming is one of the most common modes of vertebrate locomotion. In fish, segmented myotomal muscles are the primary power source, driving undulations of the body axis that transfer momentum to the water. Multiple fins and the associated fin muscles also contribute to thrust production, and stabilization and control of the swimming trajectory. We have used blood flow tracers in swimming rainbow trout (Oncorhynchus mykiss) to estimate the regional distribution of energy use across the myotomal and fin muscle groups to reveal the functional distribution of metabolic energy use within a swimming animal for the first time. Energy use by the myotomal muscle increased with speed to meet thrust requirements, particularly in posterior myotomes where muscle power outputs are greatest. At low speeds, there was high fin muscle energy use, consistent with active stability control. As speed increased, and fins were adducted, overall fin muscle energy use declined, except in the caudal fin muscles where active fin stiffening is required to maintain power transfer to the wake. The present data were obtained under steady-state conditions which rarely apply in natural, physical environments. This approach also has potential to reveal the mechanical factors that underlie changes in locomotor cost associated with movement through unsteady flow regimes. PMID:25165858

  10. Synthetic C-start maneuver in fish-like swimming

    NASA Astrophysics Data System (ADS)

    Zenit, R.; Godoy-Diana, R.

    2013-11-01

    We investigate the mechanics of the unsteady fish-like swimming maneuver using a simplified experimental model in a water tank. A flexible foil (which emulates the fish body) is impulsively actuated by rotating a cylindrical rod that holds the foil. This rod constitutes the head of the swimmer and is mounted through the shaft of the driving motor on an rail with an air bearing. The foil is initially positioned at a start angle and then rapidly rotated to a final angle, which coincides with the free-moving direction of the rail. As the foil rotates, it pushes the surrounding fluid, it deforms and stores elastic energy which drive the recovery of the straight body shape after the motor actuation has stopped; during the rotation, a trust force is induced which accelerates the array. We measure the resulting escape velocity and acceleration as a function of the beam stiffness, size, initial angle, etc. Some measurements of the velocity field during the escape were obtained using a PIV technique. The measurements agree well with a simple mechanical model that quantifies the impulse of the maneuver. The objective of this work is to understand the fundamental mechanisms of thrust generation in unsteady fast-start swimming. We acknowledge support of EADS Foundation through the project ``Fluids and elasticity in biomimetic propulsion'' and of the Chaire Total for RZ as a visiting professor at ESPCI ParisTech.

  11. Optimal swim speeds for traversing velocity barriers: An analysis of volitional high-speed swimming behavior of migratory fishes

    USGS Publications Warehouse

    Castro-Santos, T.

    2005-01-01

    Migrating fish traversing velocity barriers are often forced to swim at speeds greater than their maximum sustained speed (Ums). Failure to select an appropriate swim speed under these conditions can prevent fish from successfully negotiating otherwise passable barriers. I propose a new model of a distance-maximizing strategy for fishes traversing velocity barriers, derived from the relationships between swim speed and fatigue time in both prolonged and sprint modes. The model predicts that fish will maximize traversed distance by swimming at a constant groundspeed against a range of flow velocities, and this groundspeed is equal to the negative inverse of the slope of the swim speed-fatigue time relationship for each mode. At a predictable flow velocity, they should switch from the optimal groundspeed for prolonged mode to that for sprint mode. Data from six migratory fish species (anadromous clupeids: American shad Alosa sapidissima, alewife A. pseudoharengus and blueback herring A. aestivalis; amphidromous: striped bass Morone saxatilis; and potomodromous species: walleye (previously known as Stizostedion vitrium) and white sucker Catostomus commersonii) were used to explore the ability of fish to approximate the predicted distance-maximizing behaviors, as well as the consequences of deviating from the optima. Fish volitionally sprinted up an open-channel flume against fixed flow velocities of 1.5-4.5 m s-1, providing data on swim speeds and fatigue times, as well as their groundspeeds. Only anadromous clupeids selected the appropriate distance-maximizing groundspeed at both prolonged and sprint modes. The other three species maintained groundspeeds appropriate to the prolonged mode, even when they should have switched to the sprint optima. Because of this, these species failed to maximize distance of ascent. The observed behavioral variability has important implications both for distributional limits and fishway design.

  12. Concentration-dependent toxicity effect of SDBS on swimming behavior of freshwater fishes.

    PubMed

    Zhang, Ying; Ma, Jing; Zhou, Siyun; Ma, Fang

    2015-07-01

    Sodium dodecyl benzene sulfonate (SDBS) is a kind of widely used anionic surfactant and its discharge may pose potential risk to the receiving aquatic ecosystem. The aim of our study is to investigate the toxic effect of SDBS on fish swimming behavior quantitatively, followed by examination whether there are significant differences of swimming behavior among applied fish species (i.e. zebra fish (Danio rerio), Japanese medaka (Oryzias latipes) and red carp (Cyprinus carpio)). The swimming speed and vertical position were analyzed after the fish exposed to SDBS aiming to reflect the toxicity of SDBS on fish. Our results showed that the swimming behavior of three fishes was significantly affected by SDBS, although there were slight differences of swimming pattern changes among three fish species when they exposed to the same concentration of SDBS. It could be seen that red carp, one of the native fish species in China, can be used as a model fish to reflect the water quality changes as well as zebra fish and Japanese medaka which are commonly used as model fishes. Our study also illustrated that the swimming behavior monitoring may have a good application prospect in pre-warning of water quality.

  13. On burst-and-coast swimming performance in fish-like locomotion.

    PubMed

    Chung, M-H

    2009-09-01

    Burst-and-coast swimming performance in fish-like locomotion is studied via two-dimensional numerical simulation. The numerical method used is the collocated finite-volume adaptive Cartesian cut-cell method developed previously. The NACA00xx airfoil shape is used as an equilibrium fish-body form. Swimming in a burst-and-coast style is computed assuming that the burst phase is composed of a single tail-beat. Swimming efficiency is evaluated in terms of the mass-specific cost of transport instead of the Froude efficiency. The effects of the Reynolds number (based on the body length and burst time), duty cycle and fineness ratio (the body length over the largest thickness) on swimming performance (momentum capacity and the mass-specific cost of transport) are studied quantitatively. The results lead to a conclusion consistent with previous findings that a larval fish seldom swims in a burst-and-coast style. Given mass and swimming speed, a fish needs the least cost if it swims in a burst-and-coast style with a fineness ratio of 8.33. This energetically optimal fineness ratio is larger than that derived from the simple hydromechanical model proposed in literature. The calculated amount of energy saving in burst-and-coast swimming is comparable with the real-fish estimation in the literature. Finally, the predicted wake-vortex structures of both continuous and burst-and-coast swimming are biologically relevant.

  14. Where is the rudder of a fish?: the mechanism of swimming and control of self-propelled fish school

    NASA Astrophysics Data System (ADS)

    Wu, Chuijie; Wang, Liang

    2010-03-01

    Numerical simulation and control of self-propelled swimming of two- and three-dimensional biomimetic fish school in a viscous flow are investigated. With a parallel computational fluid dynamics package for the two- and three-dimensional moving boundary problem, which combines the adaptive multi-grid finite volume method and the methods of immersed boundary and volume of fluid, it is found that due to the interactions of vortices in the wakes, without proper control, a fish school swim with a given flapping rule can not keep the fixed shape of a queue. In order to understand the secret of fish swimming, a new feedback control strategy of fish motion is proposed for the first time, i.e., the locomotion speed is adjusted by the flapping frequency of the caudal, and the direction of swimming is controlled by the swinging of the head of a fish. Results show that with this feedback control strategy, a fish school can keep the good order of a queue in cruising, turning or swimming around circles. This new control strategy, which separates the speed control and direction control, is important in the construction of biomimetic robot fish, with which it greatly simplifies the control devices of a biomimetic robot fish.

  15. Optimal Swimming Speed in Head Currents and Effects on Distance Movement of Winter-Migrating Fish

    PubMed Central

    Brodersen, Jakob; Nilsson, P. Anders; Ammitzbøll, Jeppe; Hansson, Lars-Anders; Skov, Christian; Brönmark, Christer

    2008-01-01

    Migration is a commonly described phenomenon in nature that is often caused by spatial and temporal differences in habitat quality. However, as migration requires energy, the timing of migration may depend not only on differences in habitat quality, but also on temporal variation in migration costs. Such variation can, for instance, arise from changes in wind or current velocity for migrating birds and fish, respectively. Whereas behavioural responses of birds to such changing environmental conditions have been relatively well described, this is not the case for fish, although fish migrations are both ecologically and economically important. We here use passive and active telemetry to study how winter migrating roach regulate swimming speed and distance travelled per day in response to variations in head current velocity. Furthermore, we provide theoretical predictions on optimal swimming speeds in head currents and relate these to our empirical results. We show that fish migrate farther on days with low current velocity, but travel at a greater ground speed on days with high current velocity. The latter result agrees with our predictions on optimal swimming speed in head currents, but disagrees with previously reported predictions suggesting that fish ground speed should not change with head current velocity. We suggest that this difference is due to different assumptions on fish swimming energetics. We conclude that fish are able to adjust both swimming speed and timing of swimming activity during migration to changes in head current velocity in order to minimize energy use. PMID:18478053

  16. Swimming

    MedlinePlus

    ... eat while you swim — you could choke. continue Lakes and Ponds Lots of kids swim in streams, lakes, or ponds. Take extra care when swimming in ... can't always see the bottom of the lake or pond, so you don't always know ...

  17. Swimming kinematics and hydrodynamic imaging in the blind Mexican cave fish (Astyanax fasciatus).

    PubMed

    Windsor, Shane P; Tan, Delfinn; Montgomery, John C

    2008-09-01

    Blind Mexican cave fish (Astyanax fasciatus) lack a functioning visual system, and are known to use self-generated water motion to sense their surroundings; an ability termed hydrodynamic imaging. Nearby objects distort the flow field created by the motion of the fish. These flow distortions are sensed by the mechanosensory lateral line. Here we used image processing to measure detailed kinematics, along with a new behavioural technique, to investigate the effectiveness of hydrodynamic imaging. In a head-on approach to a wall, fish reacted to avoid collision with the wall at an average distance of only 4.0+/-0.2 mm. Contrary to previous expectation, there was no significant correlation between the swimming velocity of the fish and the distance at which they reacted to the wall. Hydrodynamic imaging appeared to be most effective when the fish were gliding with their bodies held straight, with the proportion of approaches to the wall that resulted in collision increasing from 11% to 73% if the fish were beating their tails rather than gliding as they neared the wall. The swimming kinematics of the fish were significantly different when swimming beside a wall compared with when swimming away from any walls. Blind cave fish frequently touched walls when swimming alongside them, indicating that they use both tactile and hydrodynamic information in this situation. We conclude that although hydrodynamic imaging can provide effective collision avoidance, it is a short-range sense that may often be used synergistically with direct touch.

  18. Mathematical Modeling of Space-time Variations in Acoustic Transmission and Scattering from Schools of Swim Bladder Fish (FY14 Annual Report)

    DTIC Science & Technology

    2014-09-30

    Mathematical modeling of space-time variations in acoustic transmission and scattering from schools of swim bladder fish (FY14 Annual Report...domain theory of acoustic scattering from, and propagation through, schools of swim bladder fish at and near the swim bladder resonance frequency...coupled differential equations. It incorporates a verified swim bladder scattering kernel for the individual fish, includes multiple scattering

  19. Mathematical Modeling of Space-Time Variations in Acoustic Transmission and Scattering from Schools of Swim Bladder Fish

    DTIC Science & Technology

    2015-09-30

    transmission and scattering from schools of swim bladder fish Christopher Feuillade Instituto de Física, Pontificia Universidad Católica de Chile Avenida...activities, accomplishments, and publications, of this project, which was part of the ONR Fish Acoustics Basic Research Challenge. Swim Bladder Fish...public release; distribution is unlimited. Mathematical modeling of space-time variations in acoustic transmission and scattering from schools of swim

  20. THE IPOS FRAMEWORK: LINKING FISH SWIMMING PERFORMANCE IN ALTERED FLOWS FROM LABORATORY EXPERIMENTS TO RIVERS

    SciTech Connect

    Neary, Vincent S

    2011-01-01

    Current understanding of the effects of turbulence on the swimming performance of fish 32 is primarily derived from laboratory experiments under pressurized flow swim tunnels 33 and open channel flow facilities. These studies have produced valuable information on 34 the swimming mechanics and behavior of fish in turbulent flow. However, laboratory 35 studies have limited representation of the flows fish experience in nature. The complex 36 flow structure in rivers is imparted primarily by the highly heterogeneous and non37 uniform bed and planform geometry. Our goal is to direct future laboratory and field 38 studies to adopt a common framework that will shape the integration of both approaches. 39 This paper outlines four characteristics of turbulent flow, which we suggest should be 40 evaluated when generalizing results from fish turbulent studies in both the laboratory and 41 the field. The framework is based on four turbulence characteristics that are summarized 42 under the acronym IPOS: Intensity, Periodicity, Orientation, and Scale.

  1. The rising cost of warming waters: effects of temperature on the cost of swimming in fishes.

    PubMed

    Hein, Andrew M; Keirsted, Katrina J

    2012-04-23

    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.

  2. How the body contributes to the wake in undulatory fish swimming: flow fields of a swimming eel (Anguilla anguilla).

    PubMed

    Müller, U K; Smit, J; Stamhuis, E J; Videler, J J

    2001-08-01

    Undulatory swimmers generate thrust by passing a transverse wave down their body. Thrust is generated not just at the tail, but also to a varying degree by the body, depending on the fish's morphology and swimming movements. To examine the mechanisms by which the body in particular contributes to thrust production, we chose eels, which have no pronounced tail fin and hence are thought to generate all their thrust with their body. We investigated the interaction between body movements and the flow around swimming eels using two-dimensional particle image velocimetry. Maximum flow velocities adjacent to the eel's body increase almost linearly from head to tail, suggesting that eels generate thrust continuously along their body. The wake behind eels swimming at 1.5 Ls(-1), where L is body length, consisted of a double row of double vortices with little backward momentum. The eel sheds two vortices per half tail-beat, which can be identified by their shedding dynamics as a start-stop vortex of the tail and a vortex shed when the body-generated flows reach the 'trailing edge' and cause separation. Two consecutively shed ipsilateral body and tail vortices combine to form a vortex pair that moves away from the mean path of motion. This wake shape resembles flow patterns described previously for a propulsive mode in which neither swimming efficiency nor thrust is maximised but sideways forces are high. This swimming mode is suited to high manoeuvrability. Earlier recordings show that eels also generate a wake reflective of maximum swimming efficiency. The combined findings suggest that eels can modify their body wave to generate wakes that reflect their propulsive mode.

  3. Flapping flexible fish. Periodic and secular body reconfigurations in swimming lamprey, Petromyzon marinus

    NASA Astrophysics Data System (ADS)

    Root, Robert G.; Courtland, Hayden-William; Shepherd, William; Long, John H.

    2007-11-01

    In order to analyze and model the body kinematics used by fish in a wide range of swimming behaviors, we developed a technique to separate the periodic whole-body motions that characterize steady swimming from the secular motions that characterize changes in whole-body shape. We applied this harmonic analysis technique to the study of the forward and backward swimming of lamprey. We found that in order to vary the unsteadiness of swimming, lamprey superimpose periodic and secular components of their body motion, modulate the patterns and magnitudes of those components, and change shape. These kinematic results suggest the following hydromechanical hypothesis: steady swimming is a maneuver that requires active suppression of secular body reconfigurations.

  4. Fin-Body Interaction and its Hydrodynamic Benefits in Fish's Steady Swimming

    NASA Astrophysics Data System (ADS)

    Liu, Geng; Ren, Yan; Dong, Haibo; Lauder, George

    2016-11-01

    In many past studies on fish swimming, the hydrodynamics of fish caudal fins were investigated separately. However, fish body inevitably interacts with the caudal fin since the fin flaps in the wake of the body during swimming. In this work, an integrated experimental and computational approach has been used to investigate hydrodynamic performance improvement and the vortex dynamics associated with the fin-body interactions of a jack fish in steady swimming. Realistic 3D jack fish geometry and the undulatory kinematics are reconstructed based on the output of a high-speed photogrammetry system. Hydrodynamic performance and wake structures are simulated by an in-house immersed-boundary-method flow solver. It is found that the body-fin interactions enhance the thrust production of the caudal fin by more than 30% compared to that produced by an isolated caudal fin. Further analysis on the vortex dynamics has shown that the vortices shed from the posterior part of the fish body are captured by the leading edge portion of the caudal fin. This further enhances the strength of the leading-edge vortex attaching to the caudal fin and results in larger thrust production. This work reveals a potential performance enhancement mechanism in fish's steady swimming. This work was supported by NSF CBET-1313217 and ONR MURI N00014-14-1-0533.

  5. Flow patterns of larval fish: undulatory swimming in the intermediate flow regime.

    PubMed

    Müller, Ulrike K; van den Boogaart, Jos G M; van Leeuwen, Johan L

    2008-01-01

    Fish larvae, like many adult fish, swim by undulating their body. However, their body size and swimming speeds put them in the intermediate flow regime, where viscous and inertial forces both play an important role in the interaction between fish and water. To study the influence of the relatively high viscous forces compared with adult fish, we mapped the flow around swimming zebrafish (Danio rerio) larvae using two-dimensional digital particle image velocimetry (2D-DPIV) in the horizontal and transverse plane of the fish. Fish larvae initiate a swimming bout by bending their body into a C shape. During this initial tail-beat cycle, larvae shed two vortex pairs in the horizontal plane of their wake, one during the preparatory and one during the subsequent propulsive stroke. When they swim ;cyclically' (mean swimming speed does not change significantly between tail beats), fish larvae generate a wide drag wake along their head and anterior body. The flow along the posterior body is dominated by the undulating body movements that cause jet flows into the concave bends of the body wave. Patches of elevated vorticity form around the jets, and travel posteriorly along with the body wave, until they are ultimately shed at the tail near the moment of stroke reversal. Behind the larva, two vortex pairs are formed per tail-beat cycle (the tail beating once left-to-right and then right-to-left) in the horizontal plane of the larval wake. By combining transverse and horizontal cross sections of the wake, we inferred that the wake behind a cyclically swimming zebrafish larva contains two diverging rows of vortex rings to the left and right of the mean path of motion, resembling the wake of steadily swimming adult eels. When the fish larva slows down at the end of a swimming bout, it gradually reduces its tail-beat frequency and amplitude, while the separated boundary layer and drag wake of the anterior body extend posteriorly to envelope the entire larva. This drag wake is

  6. Disentangling the Functional Roles of Morphology and Motion in the Swimming of Fish

    PubMed Central

    Tytell, Eric D.; Borazjani, Iman; Sotiropoulos, Fotis; Baker, T. Vernon; Anderson, Erik J.; Lauder, George V.

    2010-01-01

    In fishes the shape of the body and the swimming mode generally are correlated. Slender-bodied fishes such as eels, lampreys, and many sharks tend to swim in the anguilliform mode, in which much of the body undulates at high amplitude. Fishes with broad tails and a narrow caudal peduncle, in contrast, tend to swim in the carangiform mode, in which the tail undulates at high amplitude. Such fishes also tend to have different wake structures. Carangiform swimmers generally produce two staggered vortices per tail beat and a strong downstream jet, while anguilliform swimmers produce a more complex wake, containing at least two pairs of vortices per tail beat and relatively little downstream flow. Are these differences a result of the different swimming modes or of the different body shapes, or both? Disentangling the functional roles requires a multipronged approach, using experiments on live fishes as well as computational simulations and physical models. We present experimental results from swimming eels (anguilliform), bluegill sunfish (carangiform), and rainbow trout (subcarangiform) that demonstrate differences in the wakes and in swimming performance. The swimming of mackerel and lamprey was also simulated computationally with realistic body shapes and both swimming modes: the normal carangiform mackerel and anguilliform lamprey, then an anguilliform mackerel and carangiform lamprey. The gross structure of simulated wakes (single versus double vortex row) depended strongly on Strouhal number, while body shape influenced the complexity of the vortex row, and the swimming mode had the weakest effect. Performance was affected even by small differences in the wakes: both experimental and computational results indicate that anguilliform swimmers are more efficient at lower swimming speeds, while carangiform swimmers are more efficient at high speed. At high Reynolds number, the lamprey-shaped swimmer produced a more complex wake than the mackerel-shaped swimmer

  7. Disentangling the functional roles of morphology and motion in the swimming of fish.

    PubMed

    Tytell, Eric D; Borazjani, Iman; Sotiropoulos, Fotis; Baker, T Vernon; Anderson, Erik J; Lauder, George V

    2010-12-01

    In fishes the shape of the body and the swimming mode generally are correlated. Slender-bodied fishes such as eels, lampreys, and many sharks tend to swim in the anguilliform mode, in which much of the body undulates at high amplitude. Fishes with broad tails and a narrow caudal peduncle, in contrast, tend to swim in the carangiform mode, in which the tail undulates at high amplitude. Such fishes also tend to have different wake structures. Carangiform swimmers generally produce two staggered vortices per tail beat and a strong downstream jet, while anguilliform swimmers produce a more complex wake, containing at least two pairs of vortices per tail beat and relatively little downstream flow. Are these differences a result of the different swimming modes or of the different body shapes, or both? Disentangling the functional roles requires a multipronged approach, using experiments on live fishes as well as computational simulations and physical models. We present experimental results from swimming eels (anguilliform), bluegill sunfish (carangiform), and rainbow trout (subcarangiform) that demonstrate differences in the wakes and in swimming performance. The swimming of mackerel and lamprey was also simulated computationally with realistic body shapes and both swimming modes: the normal carangiform mackerel and anguilliform lamprey, then an anguilliform mackerel and carangiform lamprey. The gross structure of simulated wakes (single versus double vortex row) depended strongly on Strouhal number, while body shape influenced the complexity of the vortex row, and the swimming mode had the weakest effect. Performance was affected even by small differences in the wakes: both experimental and computational results indicate that anguilliform swimmers are more efficient at lower swimming speeds, while carangiform swimmers are more efficient at high speed. At high Reynolds number, the lamprey-shaped swimmer produced a more complex wake than the mackerel-shaped swimmer

  8. Fish Swimming: Patternsin the Mechanical Energy Generation, Transmission and Dissipation from Muscle Activation to Body Movement

    NASA Astrophysics Data System (ADS)

    Zhang, W.; Yu, Y. L.; Tong, B. G.

    2011-09-01

    The power consumption of the undulatory fish swimming is produced by active muscles. The mechanical energy generated by stimulated muscles is dissipated partly by the passive tissues of fish while it is being transmitted to the fluid medium. Furthermore, the effective energy, propelling fish movement, is a part of that delivered by the fish body. The process depends on the interactions of the active muscles, the passive tissues, and the water surrounding the fish body. In the previous works, the body-fluid interactions have been investigated widely, but it is rarely considered how the mechanical energy generates, transmits and dissipates in fish swimming. This paper addresses the regular patterns of energy transfer process from muscle activation to body movement for a cruising lamprey (LAMPREY), a kind of anguilliform swimmer. It is necessary to propose a global modelling of the kinematic chain, which is composed of active muscle force-moment model, fish-body dynamic model and hydrodynamic model in order. The present results show that there are traveling energy waves along the fish body from anterior to posterior, accompanied with energy storing and dissipating due to the viscoelastic property of internal tissues. This study is a preliminary research on the framework of kinematic chain coordination performance in fish swimming.

  9. Body fineness ratio as a predictor of maximum prolonged-swimming speed in coral reef fishes.

    PubMed

    Walker, Jeffrey A; Alfaro, Michael E; Noble, Mae M; Fulton, Christopher J

    2013-01-01

    The ability to sustain high swimming speeds is believed to be an important factor affecting resource acquisition in fishes. While we have gained insights into how fin morphology and motion influences swimming performance in coral reef fishes, the role of other traits, such as body shape, remains poorly understood. We explore the ability of two mechanistic models of the causal relationship between body fineness ratio and endurance swimming-performance to predict maximum prolonged-swimming speed (Umax ) among 84 fish species from the Great Barrier Reef, Australia. A drag model, based on semi-empirical data on the drag of rigid, submerged bodies of revolution, was applied to species that employ pectoral-fin propulsion with a rigid body at U max. An alternative model, based on the results of computer simulations of optimal shape in self-propelled undulating bodies, was applied to the species that swim by body-caudal-fin propulsion at Umax . For pectoral-fin swimmers, Umax increased with fineness, and the rate of increase decreased with fineness, as predicted by the drag model. While the mechanistic and statistical models of the relationship between fineness and Umax were very similar, the mechanistic (and statistical) model explained only a small fraction of the variance in Umax . For body-caudal-fin swimmers, we found a non-linear relationship between fineness and Umax , which was largely negative over most of the range of fineness. This pattern fails to support either predictions from the computational models or standard functional interpretations of body shape variation in fishes. Our results suggest that the widespread hypothesis that a more optimal fineness increases endurance-swimming performance via reduced drag should be limited to fishes that swim with rigid bodies.

  10. Body Fineness Ratio as a Predictor of Maximum Prolonged-Swimming Speed in Coral Reef Fishes

    PubMed Central

    Walker, Jeffrey A.; Alfaro, Michael E.; Noble, Mae M.; Fulton, Christopher J.

    2013-01-01

    The ability to sustain high swimming speeds is believed to be an important factor affecting resource acquisition in fishes. While we have gained insights into how fin morphology and motion influences swimming performance in coral reef fishes, the role of other traits, such as body shape, remains poorly understood. We explore the ability of two mechanistic models of the causal relationship between body fineness ratio and endurance swimming-performance to predict maximum prolonged-swimming speed (Umax) among 84 fish species from the Great Barrier Reef, Australia. A drag model, based on semi-empirical data on the drag of rigid, submerged bodies of revolution, was applied to species that employ pectoral-fin propulsion with a rigid body at Umax. An alternative model, based on the results of computer simulations of optimal shape in self-propelled undulating bodies, was applied to the species that swim by body-caudal-fin propulsion at Umax. For pectoral-fin swimmers, Umax increased with fineness, and the rate of increase decreased with fineness, as predicted by the drag model. While the mechanistic and statistical models of the relationship between fineness and Umax were very similar, the mechanistic (and statistical) model explained only a small fraction of the variance in Umax. For body-caudal-fin swimmers, we found a non-linear relationship between fineness and Umax, which was largely negative over most of the range of fineness. This pattern fails to support either predictions from the computational models or standard functional interpretations of body shape variation in fishes. Our results suggest that the widespread hypothesis that a more optimal fineness increases endurance-swimming performance via reduced drag should be limited to fishes that swim with rigid bodies. PMID:24204575

  11. Ontogeny of critical and prolonged swimming performance for the larvae of six Australian freshwater fish species.

    PubMed

    Kopf, S M; Humphries, P; Watts, R J

    2014-06-01

    Critical (<30 min) and prolonged (>60 min) swimming speeds in laboratory chambers were determined for larvae of six species of Australian freshwater fishes: trout cod Maccullochella macquariensis, Murray cod Maccullochella peelii, golden perch Macquaria ambigua, silver perch Bidyanus bidyanus, carp gudgeon Hypseleotris spp. and Murray River rainbowfish Melanotaenia fluviatilis. Developmental stage (preflexion, flexion, postflexion and metalarva) better explained swimming ability than did length, size or age (days after hatch). Critical speed increased with larval development, and metalarvae were the fastest swimmers for all species. Maccullochella macquariensis larvae had the highest critical [maximum absolute 46.4 cm s(-1) and 44.6 relative body lengths (L(B)) s(-1)] and prolonged (maximum 15.4 cm s(-1), 15.6 L(B) s(-1)) swimming speeds and B. bidyanus larvae the lowest critical (minimum 0.1 cm s(-1), 0.3 L(B) s(-1)) and prolonged swimming speeds (minimum 1.1 cm s(-1), 1.0 L(B) s(-1)). Prolonged swimming trials determined that the larvae of some species could not swim for 60 min at any speed, whereas the larvae of the best swimming species, M. macquariensis, could swim for 60 min at 44% of the critical speed. The swimming performance of species with precocial life-history strategies, with well-developed larvae at hatch, was comparatively better and potentially had greater ability to influence their dispersal by actively swimming than species with altricial life-history strategies, with poorly developed larvae at hatch.

  12. Hydrodynamic study of freely swimming shark fish propulsion for marine vehicles using 2D particle image velocimetry.

    PubMed

    Babu, Mannam Naga Praveen; Mallikarjuna, J M; Krishnankutty, P

    Two-dimensional velocity fields around a freely swimming freshwater black shark fish in longitudinal (XZ) plane and transverse (YZ) plane are measured using digital particle image velocimetry (DPIV). By transferring momentum to the fluid, fishes generate thrust. Thrust is generated not only by its caudal fin, but also using pectoral and anal fins, the contribution of which depends on the fish's morphology and swimming movements. These fins also act as roll and pitch stabilizers for the swimming fish. In this paper, studies are performed on the flow induced by fins of freely swimming undulatory carangiform swimming fish (freshwater black shark, L = 26 cm) by an experimental hydrodynamic approach based on quantitative flow visualization technique. We used 2D PIV to visualize water flow pattern in the wake of the caudal, pectoral and anal fins of swimming fish at a speed of 0.5-1.5 times of body length per second. The kinematic analysis and pressure distribution of carangiform fish are presented here. The fish body and fin undulations create circular flow patterns (vortices) that travel along with the body waves and change the flow around its tail to increase the swimming efficiency. The wake of different fins of the swimming fish consists of two counter-rotating vortices about the mean path of fish motion. These wakes resemble like reverse von Karman vortex street which is nothing but a thrust-producing wake. The velocity vectors around a C-start (a straight swimming fish bends into C-shape) maneuvering fish are also discussed in this paper. Studying flows around flapping fins will contribute to design of bioinspired propulsors for marine vehicles.

  13. Digesting or swimming? Integration of the postprandial metabolism, behavior and locomotion in a frequently foraging fish.

    PubMed

    Nie, Li-Juan; Cao, Zhen-Dong; Fu, Shi-Jian

    2017-02-01

    Fish that are active foragers usually perform routine activities while digesting their food; thus, their postprandial swimming capacity and related behavior adjustments might be ecologically important. To test whether digestion affect swimming performance and the relationships of digestion with metabolism and behavior in an active forager, we investigated the postprandial metabolic response, spontaneous swimming activities, critical swimming speed (Ucrit), and fast-start escape performance of both fasted and digesting (3h after feeding to satiation) juvenile rose bitterling (Rhodeus ocellatus). Feeding to satiation elicited a 50% increase in the oxygen consumption rate, which peaked at 3h after feeding and returned to the prefeeding state after another 3h. However, approximately 50% and 90% of individuals resumed feeding behavior at 2 and 3h postfeeding, respectively, although the meal size varied substantially. Digestion showed no effect on either steady swimming performance as suggested by the Ucrit or unsteady swimming performance indicated by the maximum linear velocity in fast-start escape movement. However, digesting fish showed more spontaneous activity as indicated by the longer total distance traveled, mainly through an increased percentage of time spent moving (PTM). A further analysis found that fasting individuals with high swimming speed were more inclined to increase their PTM during digestive processes. The present study suggests that as an active forager With a small meal size and hence limited postprandial physiological and morphological changes, the swimming performance of rose bitterling is maintained during digestion, which might be crucial for its active foraging mode and anti-predation strategy. Copyright © 2016 Elsevier Inc. All rights reserved.

  14. Mosquitofish (Gambusia affinis) responds differentially to a robotic fish of varying swimming depth and aspect ratio.

    PubMed

    Polverino, Giovanni; Porfiri, Maurizio

    2013-08-01

    In this study, we explore the feasibility of using bioinspired robotics to influence the behaviour of mosquitofish (Gambusia affinis), a social freshwater fish species that is extensively studied for the ecological issues associated with its diffusion in non-native environments. Specifically, in a dichotomous choice test, we investigate the behavioural response of small shoals of mosquitofish to a robotic fish inspired by mosquitofish in its colouration, shape, aspect ratio, and locomotion. Our results indicate that the swimming depth and the aspect ratio of the robotic fish are both determinants of mosquitofish preference. In particular, we find that mosquitofish are never attracted by a robotic fish whose colouration and shape are inspired by live subjects and that the degree of repulsion varies as a function of the swimming depth and the aspect ratio.

  15. Body dynamics and hydrodynamics of swimming fish larvae: a computational study.

    PubMed

    Li, Gen; Müller, Ulrike K; van Leeuwen, Johan L; Liu, Hao

    2012-11-15

    To understand the mechanics of fish swimming, we need to know the forces exerted by the fluid and how these forces affect the motion of the fish. To this end, we developed a 3-D computational approach that integrates hydrodynamics and body dynamics. This study quantifies the flow around a swimming zebrafish (Danio rerio) larva. We used morphological and kinematics data from actual fish larvae aged 3 and 5 days post fertilization as input for a computational model that predicted free-swimming dynamics from prescribed changes in body shape. We simulated cyclic swimming and a spontaneous C-start. A rigorous comparison with 2-D particle image velocimetry and kinematics data revealed that the computational model accurately predicted the motion of the fish's centre of mass as well as the spatial and temporal characteristics of the flow. The distribution of pressure and shear forces along the body showed that thrust is mainly produced in the posterior half of the body. We also explored the effect of the body wave amplitude on swimming performance by considering wave amplitudes that were up to 40% larger or smaller than the experimentally observed value. Increasing the body wave amplitude increased forward swimming speed from 7 to 21 body lengths per second, which is consistent with experimental observations. The model also predicted a non-linear increase in propulsive efficiency from 0.22 to 0.32 while the required mechanical power quadrupled. The efficiency increase was only minor for wave amplitudes above the experimental reference value, whereas the cost of transport rose significantly.

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

    PubMed Central

    Polverino, Giovanni; Phamduy, Paul; Porfiri, Maurizio

    2013-01-01

    The possibility of integrating bioinspired robots in groups of live social animals may constitute a valuable tool to study the basis of social behavior and uncover the fundamental determinants of animal functions and dysfunctions. In this study, we investigate the interactions between individual golden shiners (Notemigonus crysoleucas) and robotic fish swimming together in a water tunnel at constant flow velocity. The robotic fish is designed to mimic its live counterpart in the aspect ratio, body shape, dimension, and locomotory pattern. Fish positional preference with respect to the robot is experimentally analyzed as the robot's color pattern and tail-beat frequency are varied. Behavioral observations are corroborated by particle image velocimetry studies aimed at investigating the flow structure behind the robotic fish. Experimental results show that the time spent by golden shiners in the vicinity of the bioinspired robotic fish is the highest when the robot mimics their natural color pattern and beats its tail at the same frequency. In these conditions, fish tend to swim at the same depth of the robotic fish, where the wake from the robotic fish is stronger and hydrodynamic return is most likely to be effective. PMID:24204882

  17. Fish and robots swimming together in a water tunnel: robot color and tail-beat frequency influence fish behavior.

    PubMed

    Polverino, Giovanni; Phamduy, Paul; Porfiri, Maurizio

    2013-01-01

    The possibility of integrating bioinspired robots in groups of live social animals may constitute a valuable tool to study the basis of social behavior and uncover the fundamental determinants of animal functions and dysfunctions. In this study, we investigate the interactions between individual golden shiners (Notemigonus crysoleucas) and robotic fish swimming together in a water tunnel at constant flow velocity. The robotic fish is designed to mimic its live counterpart in the aspect ratio, body shape, dimension, and locomotory pattern. Fish positional preference with respect to the robot is experimentally analyzed as the robot's color pattern and tail-beat frequency are varied. Behavioral observations are corroborated by particle image velocimetry studies aimed at investigating the flow structure behind the robotic fish. Experimental results show that the time spent by golden shiners in the vicinity of the bioinspired robotic fish is the highest when the robot mimics their natural color pattern and beats its tail at the same frequency. In these conditions, fish tend to swim at the same depth of the robotic fish, where the wake from the robotic fish is stronger and hydrodynamic return is most likely to be effective.

  18. Swimming

    MedlinePlus

    ... hurt your neck very badly. Test the pool's water temperature before you plunge in. Cold water can shock your body and make your blood ... t swim in the dark. Go into the water slowly to make sure the temperature feels comfortable and it's not too cold. If ...

  19. Effects of crude oil and dispersed crude oil on the critical swimming speed of puffer fish, Takifugu rubripes.

    PubMed

    Yu, Xiaoming; Xu, Chuancai; Liu, Haiying; Xing, Binbin; Chen, Lei; Zhang, Guosheng

    2015-05-01

    In order to examine the effects of crude oil and dispersed crude oil (DCO) on the swimming ability of puffer fish, Takifugu rubripes, the critical swimming speeds (U crit) of fish exposed to different concentrations of water-soluble fraction (WSF) of crude oil and DCO solution were determined in a swimming flume. WSF and DCO significantly affected the U crit of puffer fish (p < 0.05). The U crit of puffer fish exposed to 136 mg L(-1) WSF and 56.4 mg L(-1) DCO decreased 48.7 % and 43.4 %, respectively. DCO was more toxic to puffer fish than WSF. These results suggested that crude oil and chemically dispersed oil could weaken the swimming ability of puffer fish.

  20. Fish-robot interactions in a free-swimming environment: Effects of speed and configuration of robots on live fish

    NASA Astrophysics Data System (ADS)

    Butail, Sachit; Polverino, Giovanni; Phamduy, Paul; Del Sette, Fausto; Porfiri, Maurizio

    2014-03-01

    We explore fish-robot interactions in a comprehensive set of experiments designed to highlight the effects of speed and configuration of bioinspired robots on live zebrafish. The robot design and movement is inspired by salient features of attraction in zebrafish and includes enhanced coloration, aspect ratio of a fertile female, and carangiform/subcarangiformlocomotion. The robots are autonomously controlled to swim in circular trajectories in the presence of live fish. Our results indicate that robot configuration significantly affects both the fish distance to the robots and the time spent near them.

  1. Thermal acclimation effects differ between voluntary, maximum, and critical swimming velocities in two cyprinid fishes.

    PubMed

    O'Steen, Shyril; Bennett, Albert F

    2003-01-01

    Temperature acclimation may be a critical component of the locomotor physiology and ecology of ectothermic animals, particularly those living in eurythermal environments. Several studies of fish report striking acclimation of biochemical and kinetic properties in isolated muscle. However, the relatively few studies of whole-animal performance report variable acclimation responses. We test the hypothesis that different types of whole-animal locomotion will respond differently to temperature acclimation, probably due to divergent physiological bases of locomotion. We studied two cyprinid fishes, tinfoil barbs (Puntius schwanenfeldii) and river barbels (Barbus barbus). Study fish were acclimated to either cold or warm temperatures for at least 6 wk and then assayed at four test temperatures for three types of swimming performance. We measured voluntary swimming velocity to estimate routine locomotor behavior, maximum fast start velocity to estimate anaerobic capacity, and critical swimming velocity to estimate primarily aerobic capacity. All three performance measures showed some acute thermal dependence, generally a positive correlation between swimming speed and test temperature. However, each performance measure responded quite differently to acclimation. Critical speeds acclimated strongly, maximum speeds not at all, and voluntary speeds uniquely in each species. Thus we conclude that long-term temperature exposure can have very different consequences for different types of locomotion, consistent with our hypothesis. The data also address previous hypotheses that predict that polyploid and eurythermal fish will have greater acclimation abilities than other fish, due to increased genetic flexibility and ecological selection, respectively. Our results conflict with these predictions. River barbels are eurythermal polyploids and tinfoil barbs stenothermal diploids, yet voluntary swimming acclimated strongly in tinfoil barbs and minimally in river barbels, and

  2. Speed limits on swimming of fishes and cetaceans.

    PubMed

    Iosilevskii, G; Weihs, D

    2008-03-06

    Physical limits on swimming speed of lunate tail propelled aquatic animals are proposed. A hydrodynamic analysis, applying experimental data wherever possible, is used to show that small swimmers (roughly less than a metre long) are limited by the available power, while larger swimmers at a few metres below the water surface are limited by cavitation. Depending on the caudal fin cross-section, 10-15 m s(-1) is shown to be the maximum cavitation-free velocity for all swimmers at a shallow depth.

  3. Advances in the Visualization and Analysis of Boundary Layer Flow in Swimming Fish

    DTIC Science & Technology

    2005-02-01

    3.1.1 Fish Scup, Stenotomus chrysops, (n = 9) and smooth dogfish , Mustelus canis, (n = 1), were caught in traps or by hook and line in Nantucket Sound...the experiments. The body length, L, of scup averaged 19.5 ± 1.8 cm (mean ± S.D.). The dogfish measured 44.4 cm. 3.1.2 Swimming conditions Scup were...The dogfish was observed swimming 20 - 65 cm s" in the flume at 22 - 23 C. In flume trials, observations from three positions along the midline of each

  4. Passive and Active Flow Control by Swimming Fishes and Mammals

    NASA Astrophysics Data System (ADS)

    Fish, F. E.; Lauder, G. V.

    2006-01-01

    What mechanisms of flow control do animals use to enhance hydrodynamic performance? Animals are capable of manipulating flow around the body and appendages both passively and actively. Passive mechanisms rely on structural and morphological components of the body (i.e., humpback whale tubercles, riblets). Active flow control mechanisms use appendage or body musculature to directly generate wake flow structures or stiffen fins against external hydrodynamic loads. Fish can actively control fin curvature, displacement, and area. The vortex wake shed by the tail differs between eel-like fishes and fishes with a discrete narrowing of the body in front of the tail, and three-dimensional effects may play a major role in determining wake structure in most fishes.

  5. Learning to swim, again: Axon regeneration in fish.

    PubMed

    Rasmussen, Jeffrey P; Sagasti, Alvaro

    2017-01-01

    Damage to the central nervous system (CNS) of fish can often be repaired to restore function, but in mammals recovery from CNS injuries usually fails due to a lack of axon regeneration. The relatively growth-permissive environment of the fish CNS may reflect both the absence of axon inhibitors found in the mammalian CNS and the presence of pro-regenerative environmental factors. Despite their different capacities for axon regeneration, many of the physiological processes, intrinsic molecular pathways, and cellular behaviors that control an axon's ability to regrow are conserved between fish and mammals. Fish models have thus been useful both for identifying factors differing between mammals and fish that may account for differences in CNS regeneration and for characterizing conserved intrinsic pathways that regulate axon regeneration in all vertebrates. The majority of adult axon regeneration studies have focused on the optic nerve or spinal axons of the teleosts goldfish and zebrafish, which have been productive models for identifying genes associated with axon regeneration, cellular mechanisms of circuit reestablishment, and the basis of functional recovery. Lampreys, which are jawless fish lacking myelin, have provided an opportunity to study regeneration of well defined spinal cord circuits. Newer larval zebrafish models offer numerous genetic tools and the ability to monitor the dynamic behaviors of extrinsic cell types regulating axon regeneration in live animals. Recent advances in imaging and gene editing methods are making fish models yet more powerful for investigating the cellular and molecular underpinnings of axon regeneration. Copyright © 2016 Elsevier Inc. All rights reserved.

  6. The role of mechanical resonance in the neural control of swimming in fishes.

    PubMed

    Tytell, Eric D; Hsu, Chia-Yu; Fauci, Lisa J

    2014-02-01

    The bodies of many fishes are flexible, elastic structures; if you bend them, they spring back. Therefore, they should have a resonant frequency: a bending frequency at which the output amplitude is maximized for a particular input. Previous groups have hypothesized that swimming at this resonant frequency could maximize efficiency, and that a neural circuit called the central pattern generator might be able to entrain to a mechanical resonance. However, fishes swim in water, which may potentially damp out many resonant effects. Additionally, their bodies are elongated, which means that bending can occur in complicated ways along the length of the body. We review previous studies of the mechanical properties of fish bodies, and then present new data that demonstrate complex bending properties of elongated fish bodies. Resonant peaks in amplitude exist, but there may be many of them depending on the body wavelength. Additionally, they may not correspond to the maximum swimming speed. Next, we describe experiments using a closed-loop preparation of the lamprey, in which a preparation of the spinal cord is linked to a real-time simulation of the muscle and body properties, allowing us to examine resonance entrainment as we vary the simulated resonant frequency. We find that resonance entrainment does occur, but is rare. Gain had a significant, though weak, effect, and a nonlinear muscle model produced resonance entrainment more often than a linear filter. We speculate that resonance may not be a critical effect for efficient swimming in elongate, anguilliform swimmers, though it may be more important for stiffer carangiform and thunniform fishes. Copyright © 2014 Elsevier GmbH. All rights reserved.

  7. A fish-like robot: Mechanics of swimming due to constraints

    NASA Astrophysics Data System (ADS)

    Tallapragada, Phanindra; Malla, Rijan

    2014-11-01

    It is well known that due to reasons of symmetry, a body with one degree of actuation cannot swim in an ideal fluid. However certain velocity constraints arising in fluid-body interactions, such as the Kutta condition classically applied at the trailing cusp of a Joukowski hydrofoil break this symmetry through vortex shedding. Thus Joukowski foils that vary shape periodically can be shown to be able to swim through vortex shedding. In general it can be shown that vortex shedding due to the Kutta condition is equivalent to nonintegrable constraints arising in the mechanics of finite-dimensional mechanical systems. This equivalence allows hydrodynamic problems involving vortex shedding, especially those pertaining to swimming and related phenomena to be framed in the context of geometric mechanics on manifolds. This formal equivalence also allows the design of bio inspired robots that swim not due to shape change but due to internal moving masses and rotors. Such robots lacking articulated joints are easy to design, build and control. We present such a fish-like robot that swims due to the rotation of internal rotors.

  8. Large-amplitude undulatory fish swimming: fluid mechanics coupled to internal mechanics.

    PubMed

    Pedley, T J; Hill, S J

    1999-12-01

    The load against which the swimming muscles contract, during the undulatory swimming of a fish, is composed principally of hydrodynamic pressure forces and body inertia. In the past this has been analysed, through an equation for bending moments, for small-amplitude swimming, using Lighthill's elongated-body theory and a 'vortex-ring panel method', respectively, to compute the hydrodynamic forces. Those models are outlined in this review, and a summary is given of recent work on large-amplitude swimming that has (a) extended the bending moment equation to large amplitude, which involves the introduction of a new (though probably usually small) term, and (b) developed a large-amplitude vortex-ring panel method. The latter requires computation of the wake, which rolls up into concentrated vortex rings and filaments, and has a significant effect on the pressure on the body. Application is principally made to the saithe (Pollachius virens). The calculations confirm that the wave of muscle activation travels down the fish much more rapidly than the wave of bending.

  9. Three-dimensional flow structures and vorticity control in fish-like swimming

    NASA Astrophysics Data System (ADS)

    Zhu, Q.; Wolfgang, M. J.; Yue, D. K. P.; Triantafyllou, M. S.

    2002-10-01

    We employ a three-dimensional, nonlinear inviscid numerical method, in conjunction with experimental data from live fish and from a fish-like robotic mechanism, to establish the three-dimensional features of the flow around a fish-like body swimming in a straight line, and to identify the principal mechanisms of vorticity control employed in fish-like swimming. The computations contain no structural model for the fish and hence no recoil correction. First, we show the near-body flow structure produced by the travelling-wave undulations of the bodies of a tuna and a giant danio. As revealed in cross-sectional planes, for tuna the flow contains dominant features resembling the flow around a two-dimensional oscillating plate over most of the length of the fish body. For the giant danio, on the other hand, a mixed longitudinal transverse structure appears along the hind part of the body. We also investigate the interaction of the body-generated vortices with the oscillating caudal fin and with tail-generated vorticity. Two distinct vorticity interaction modes are identified: the first mode results in high thrust and is generated by constructive pairing of body-generated vorticity with same-sign tail-generated vorticity, resulting in the formation of a strong thrust wake; the second corresponds to high propulsive efficiency and is generated by destructive pairing of body-generated vorticity with opposite-sign tail-generated vorticity, resulting in the formation of a weak thrust wake.

  10. Fish and robots swimming together: attraction towards the robot demands biomimetic locomotion.

    PubMed

    Marras, Stefano; Porfiri, Maurizio

    2012-08-07

    The integration of biomimetic robots in a fish school may enable a better understanding of collective behaviour, offering a new experimental method to test group feedback in response to behavioural modulations of its 'engineered' member. Here, we analyse a robotic fish and individual golden shiners (Notemigonus crysoleucas) swimming together in a water tunnel at different flow velocities. We determine the positional preference of fish with respect to the robot, and we study the flow structure using a digital particle image velocimetry system. We find that biomimetic locomotion is a determinant of fish preference as fish are more attracted towards the robot when its tail is beating rather than when it is statically immersed in the water as a 'dummy'. At specific conditions, the fish hold station behind the robot, which may be due to the hydrodynamic advantage obtained by swimming in the robot's wake. This work makes a compelling case for the need of biomimetic locomotion in promoting robot-animal interactions and it strengthens the hypothesis that biomimetic robots can be used to study and modulate collective animal behaviour.

  11. Fish and robots swimming together: attraction towards the robot demands biomimetic locomotion

    PubMed Central

    Marras, Stefano; Porfiri, Maurizio

    2012-01-01

    The integration of biomimetic robots in a fish school may enable a better understanding of collective behaviour, offering a new experimental method to test group feedback in response to behavioural modulations of its ‘engineered’ member. Here, we analyse a robotic fish and individual golden shiners (Notemigonus crysoleucas) swimming together in a water tunnel at different flow velocities. We determine the positional preference of fish with respect to the robot, and we study the flow structure using a digital particle image velocimetry system. We find that biomimetic locomotion is a determinant of fish preference as fish are more attracted towards the robot when its tail is beating rather than when it is statically immersed in the water as a ‘dummy’. At specific conditions, the fish hold station behind the robot, which may be due to the hydrodynamic advantage obtained by swimming in the robot's wake. This work makes a compelling case for the need of biomimetic locomotion in promoting robot–animal interactions and it strengthens the hypothesis that biomimetic robots can be used to study and modulate collective animal behaviour. PMID:22356819

  12. Individual variation in the swimming performance of fishes: An overlooked source of variation in toxicity studies

    SciTech Connect

    Kolok, A.S. ||; Plaisance, E.P.; Abdelghani, A.

    1998-02-01

    A commonly used indicator of sublethal stress in fish is impaired swimming performance. Analysis of performance data usually employs a simple comparison, in which the mean of a stressed group of fish is compared to that of a control group. Although such a comparison is satisfactory in many cases, a comparison emphasizing individual variation in performance can yield valuable information unattainable by a means comparison. In this experiment, the authors determined critical swimming speeds of subadult male fathead minnows before and after exposure to contaminated sediments from Devil`s Swamp, Louisiana, USA. The data were then analyzed using a means comparison and an individual approach to illustrate the differences in explanatory power between the two approaches.

  13. Swimming behaviour of fish under diminished gravity conditions - a review

    NASA Astrophysics Data System (ADS)

    Anken, Ralf; Hilbig, Reinhard; Anken, Ralf

    In vertebrates (including humans) altered gravitational environments (∆g) such as weightlessness (microgravity, µg) can induce malfunctions of the inner ears leading to severe sensorymotor disorders (intersensory-conflict-theory) including space motion sickness (SMS), a kinetosis. SMS is an important operational problem, since the sensorimotor performance of an affected astronaut is severely impaired especially in the first two to three days of a space mission. Of course human subjects are not amenable to invasive research techniques for studying the basis of SMS and related kinetoses. Other vertebrates such as fish are therefore used as model systems since their peripheral and central vestibular system - at least at the level of primary vestibular brain nuclei - is largely homologous to that of humans. Moreover, fish are capable to maintain spatial orientation and postural control in 3 dimensions even in dark or turbid waters, because they are particularly sensitive to ∆g. The observations made, using fish as a model system, to contribute to the understanding of human kinetosis susceptibility will be reviewed. A conclusion will address lessions learned. Acknowledgement: Numerous of the studies to be reviewed were financially supported by the German Aerospace Center (DLR) (FKZ: 50 WB 9997/50 WB 0527).

  14. Different ossification patterns of intermuscular bones in fish with different swimming modes

    PubMed Central

    Yao, Wenjie; Lv, Yaoping; Gong, Xiaoling; Wu, Jiaming; Bao, Baolong

    2015-01-01

    ABSTRACT Intermuscular bones are found in the myosepta in teleosts. However, there is very little information on the development and ossification of these intermuscular bones. In this study, we performed an in-depth investigation of the ossification process during development in zebrafish (Danio rerio) and Japanese eel (Anguilla japonica). In Japanese eel, a typical anguilliform swimmer, the intermuscular bones ossified predominantly from the anterior to the posterior. By contrast, in the zebrafish, a sub-carangiform or carangiform swimmer, the intermuscular bones ossified predominantly from the posterior to the anterior regions of the fish. Furthermore, tail amputation affected the ossification of the intermuscular bones. The length of the intermuscular bones in the posterior area became significantly shorter in tail-amputated zebrafish and Japanese eels, and both had less active and lower swimming speeds; this indicates that swimming might induce the ossification of the intermuscular bones. Moreover, when a greater length of tail was amputated in the zebrafish, the intermuscular bones became even shorter. Tail amputation affected the length and ossification of intermuscular bones in the anterior part of the fish, close to the head, differently between the two fish: they became significantly shorter in the zebrafish, but did not in the Japanese eel. This might be because tail amputation did not significantly affect the undulations in the anterior of the Japanese eel, especially near the head. This study shows that the ossification of intermuscular bones might be induced through mechanical force loadings that are produced by swimming. PMID:26603470

  15. Parametric study of the swimming performance of a fish robot propelled by a flexible caudal fin.

    PubMed

    Low, K H; Chong, C W

    2010-12-01

    In this paper, we aim to study the swimming performance of fish robots by using a statistical approach. A fish robot employing a carangiform swimming mode had been used as an experimental platform for the performance study. The experiments conducted aim to investigate the effect of various design parameters on the thrust capability of the fish robot with a flexible caudal fin. The controllable parameters associated with the fin include frequency, amplitude of oscillation, aspect ratio and the rigidity of the caudal fin. The significance of these parameters was determined in the first set of experiments by using a statistical approach. A more detailed parametric experimental study was then conducted with only those significant parameters. As a result, the parametric study could be completed with a reduced number of experiments and time spent. With the obtained experimental result, we were able to understand the relationship between various parameters and a possible adjustment of parameters to obtain a higher thrust. The proposed statistical method for experimentation provides an objective and thorough analysis of the effects of individual or combinations of parameters on the swimming performance. Such an efficient experimental design helps to optimize the process and determine factors that influence variability.

  16. The effects of caudal fin loss and regeneration on the swimming performance of three cyprinid fish species with different swimming capacities.

    PubMed

    Fu, Cheng; Cao, Zhen-Dong; Fu, Shi-Jian

    2013-08-15

    In nature, the caudal fins of fish species are frequently lost to some extent by aggressive behaviour, predation and diseases. To test whether the swimming performance of fish with different swimming capacities would be differentially affected due to caudal fin loss and regeneration, we investigated the critical swimming speed (Ucrit), swimming metabolic rate (M(O2)), tail beat frequency (f(TB)) and tail beat amplitude (A(TB)) after caudal fin loss and regeneration (20 days) in juveniles of three cyprinid fish species: the qingbo (Spinibarbus sinensis; strong swimmer), the common carp (Cyprinus carpio; intermediate swimmer) and the goldfish (Carassius auratus; poor swimmer). The Ucrit values of the caudal-fin-lost qingbo, common carp and goldfish were 49, 32 and 35% significantly lower than those of the control groups, respectively. The maximum tail beat amplitude (A(TBmax)) (all three fishes), the maximum tail beat frequency (f(TBmax)) (only the common carp and the goldfish) and/or the active metabolic rate (M(O2active)) (only the common carp) of the caudal-fin-lost fish were significantly higher than those of the control groups. After 20 days of recovery, the caudal fins recovered to 41, 47 and 24% of those of the control groups for the qingbo, the common carp and the goldfish, respectively. However, the Ucrit values of the fin-regenerated qingbo, common carp and goldfish recovered to 86, 91 and 95% of those of the control group, respectively. The caudal-fin-regenerated qingbo and common carp showed a significantly higher A(TBmax) and f(TBmax), respectively, compared with those of the control groups. The qingbo had a higher f(TBmax) but a lower A(TBmax) than the common carp and the goldfish, which suggested that a strong swimmer may maintain swimming speed primarily by maintaining a greater f(TBmax), for which the caudal fin plays a more important role during swimming, than a poor swimmer. The M(O2active) of fish (common carp) with a redundant respiratory

  17. Go reconfigure: how fish change shape as they swim and evolve.

    PubMed

    Long, John H; Porter, Marianne E; Root, Robert G; Liew, Chun Wai

    2010-12-01

    The bodies of fish change shape over propulsive, behavioral, developmental, and evolutionary time scales, a general phenomenon that we call "reconfiguration". Undulatory, postural, and form-reconfiguration can be distinguished, studied independently, and examined in terms of mechanical interactions and evolutionary importance. Using a combination of live, swimming fishes and digital robotic fish that are autonomous and self-propelled, we examined the functional relation between undulatory and postural reconfiguration in forward swimming, backward swimming, and yaw turning. To probe how postural and form reconfiguration interact, the yaw turning of leopard sharks was examined using morphometric and kinematic analyses. To test how undulatory reconfiguration might evolve, the digital robotic fish were subjected to selection for enhanced performance in a simulated ecology in which each individual had to detect and move towards a food source. In addition to the general issue of reconfiguration, these investigations are united by the fact that the dynamics of undulatory and postural reconfigurations are predicted to be determined, in part, by the structural stiffness of the fish's body. Our method defines undulatory reconfiguration as the combined, point-by-point periodic motion of the body, leaving postural reconfiguration as the combined deviations from undulatory reconfiguration. While undulatory reconfiguration appears to be the sole or primary propulsive driver, postural reconfiguration may contribute to propulsion in hagfish and it is correlated with differences in forward, and backward, swimming in lamprey. Form reconfigures over developmental time in leopard sharks in a manner that is consistent with an allometric scaling theory in which structural stiffness of the body is held constant. However, correlation of a form proxy for structural stiffness of the body suggests that body stiffness may scale in order to limit maximum postural reconfiguration during routine

  18. Fish optimize sensing and respiration during undulatory swimming

    PubMed Central

    Akanyeti, O.; Thornycroft, P. J. M.; Lauder, G. V.; Yanagitsuru, Y. R.; Peterson, A. N.; Liao, J. C.

    2016-01-01

    Previous work in fishes considers undulation as a means of propulsion without addressing how it may affect other functions such as sensing and respiration. Here we show that undulation can optimize propulsion, flow sensing and respiration concurrently without any apparent tradeoffs when head movements are coupled correctly with the movements of the body. This finding challenges a long-held assumption that head movements are simply an unintended consequence of undulation, existing only because of the recoil of an oscillating tail. We use a combination of theoretical, biological and physical experiments to reveal the hydrodynamic mechanisms underlying this concerted optimization. Based on our results we develop a parsimonious control architecture that can be used by both undulatory animals and machines in dynamic environments. PMID:27009352

  19. Fish optimize sensing and respiration during undulatory swimming.

    PubMed

    Akanyeti, O; Thornycroft, P J M; Lauder, G V; Yanagitsuru, Y R; Peterson, A N; Liao, J C

    2016-03-24

    Previous work in fishes considers undulation as a means of propulsion without addressing how it may affect other functions such as sensing and respiration. Here we show that undulation can optimize propulsion, flow sensing and respiration concurrently without any apparent tradeoffs when head movements are coupled correctly with the movements of the body. This finding challenges a long-held assumption that head movements are simply an unintended consequence of undulation, existing only because of the recoil of an oscillating tail. We use a combination of theoretical, biological and physical experiments to reveal the hydrodynamic mechanisms underlying this concerted optimization. Based on our results we develop a parsimonious control architecture that can be used by both undulatory animals and machines in dynamic environments.

  20. Size and cell number of the utricle in kinetotically swimming fish: a parabolic aircraft flight study

    NASA Astrophysics Data System (ADS)

    Bäuerle, A.; Anken, R. H.; Hilbig, R.; Baumhauer, N.; Rahmann, H.

    2004-01-01

    Humans taking part in parabolic aircraft flights (PAFs) may suffer from space motion sickness (SMS, a kinetosis). Since it has been repeatedly shown earlier that some fish of a given batch also reveal a kinetotic behavior during PAFs (especially so-called spinning movements and looping responses) and due to the homology of the vestibular apparatus among all vertebrates, fish can be used as model systems to investigate the origin of susceptibility to motion sickness. Therefore, we examined the utricular maculae (they are responsible for the internalization of gravity in teleosteans) of fish swimming kinetotically at microgravity in comparison with animals from the same batch who swam normally. On the histological level, it was found that the total number of both sensory and supporting cells of the utricular maculae did not differ between kinetotic animals as compared to normally swimming fish. Cell density (sensory and supporting cells/100 μm 2), however, was reduced in kinetotic animals ( p < 0.0001), which seemed to be due to malformed epithelial cells (increase in cell size) of the kinetotic specimens. Susceptibility to kinetoses may therefore originate in malformed sensory epithelia.

  1. Size and Cell Number of the Utricle in kinetotically swimming Fish: A parabolic Aircraft Flight Study

    NASA Astrophysics Data System (ADS)

    Baeuerle, A.; Anken, R.; Baumhauer, N.; Hilbig, R.; Rahmann, H.

    Humans taking part in parabolic aircraft flights (PAFs) may suffer from space motion sickness (SMS, a kinetosis). Since it has been repeatedly shown earlier that some fish of a given batch also reveal a kinetotic behaviour during PAFs (especially so-called spinning movements and looping responses), and due to the homology of the vestibular apparatus among all vertebrates, fish can be used as model systems to investigate the origin of susceptibility to motion sickness. Therefore, we examined the utricular maculae (they are responsible for the internalisation of gravity in teleosteans) of fish swimming kinetotically during the μg-phases in the course of PAFs in comparison with animals from the same batch who swam normally. On the light microscopical level, it was found that the total number of both sensory and supporting cells of the utricular maculae did not differ between kinetotic animals as compared to normally swimming fish. Cell density (sensory and supporting cells/100μm -μm), however, was reduced in kinetotic animals (p<0.0001), which seemed to be due to malformed epithelial cells (increase in cell size) of the kinetotic specimens. Susceptibility to kinetoses may therefore originate in asymmetric inner ear otoliths as has been suggested earlier, but also in genetically predispositioned, malformed sensory epithelia. This work was financially supported by the German Aerospace Center (DLR) e.V. (FKZ: 50 WB 9997).

  2. Statistics of the electrosensory input in the freely swimming weakly electric fish Apteronotus leptorhynchus.

    PubMed

    Fotowat, Haleh; Harrison, Reid R; Krahe, Rüdiger

    2013-08-21

    The neural computations underlying sensory-guided behaviors can best be understood in view of the sensory stimuli to be processed under natural conditions. This input is often actively shaped by the movements of the animal and its sensory receptors. Little is known about natural sensory scene statistics taking into account the concomitant movement of sensory receptors in freely moving animals. South American weakly electric fish use a self-generated quasi-sinusoidal electric field for electrolocation and electrocommunication. Thousands of cutaneous electroreceptors detect changes in the transdermal potential (TDP) as the fish interact with conspecifics and the environment. Despite substantial knowledge about the circuitry and physiology of the electrosensory system, the statistical properties of the electrosensory input evoked by natural swimming movements have never been measured directly. Using underwater wireless telemetry, we recorded the TDP of Apteronotus leptorhynchus as they swam freely by themselves and during interaction with a conspecific. Swimming movements caused low-frequency TDP amplitude modulations (AMs). Interacting with a conspecific caused additional AMs around the difference frequency of their electric fields, with the amplitude of the AMs (envelope) varying at low frequencies due to mutual movements. Both AMs and envelopes showed a power-law relationship with frequency, indicating spectral scale invariance. Combining a computational model of the electric field with video tracking of movements, we show that specific swimming patterns cause characteristic spatiotemporal sensory input correlations that contain information that may be used by the brain to guide behavior.

  3. Assessing possible effects of fish-culture systems on fish swimming: the role of stability in turbulent flows.

    PubMed

    Webb, Paul W; Cotel, Aline J

    2011-06-01

    Fish are cultured in ponds, recirculating systems, raceways, and cages. Turbulence is associated with one or more of mechanisms to facilitate food accessibility, maintain adequate levels of oxygen, remove carbon dioxide, urinary and fecal wastes, as well as from locomotion of fishes themselves. Turbulence has been shown to have positive and negative effects on fish swimming, feeding, and energetics, usually with negative impacts at very low and at high levels, and least effects and sometimes positive effects at intermediate levels. Differences in responses of fishes with varying levels of turbulence are related to the size of eddies relative to the size of a fish (larvae, juveniles, and adults). Impacts on locomotor functions are associated with eddy diameters of the order of 0.5-1L, where L is the total length of a fish. Negative locomotor impacts of turbulence are associated with eddies challenging stability, while positive effects promote drafting and station holding with reduced locomotor motions. Deployment of control surfaces increases with the level of turbulence up to a threshold where control is overwhelmed. The design of culture facilities is expected to affect levels of turbulence and may be engineered to provide optimal levels facilitating high growth.

  4. Lateral Line Layout Correlates with the Differential Hydrodynamic Pressure on Swimming Fish

    NASA Astrophysics Data System (ADS)

    Ristroph, Leif; Liao, James C.; Zhang, Jun

    2015-01-01

    The lateral line of fish includes the canal subsystem that detects hydrodynamic pressure gradients and is thought to be important in swimming behaviors such as rheotaxis and prey tracking. Here, we explore the hypothesis that this sensory system is concentrated at locations where changes in pressure are greatest during motion through water. Using high-fidelity models of rainbow trout, we mimic the flows encountered during swimming while measuring pressure with fine spatial and temporal resolution. The variations in pressure for perturbations in body orientation and for disturbances to the incoming stream are seen to correlate with the sensory network. These findings support a view of the lateral line as a "hydrodynamic antenna" that is configured to retrieve flow signals and also suggest a physical explanation for the nearly universal sensory layout across diverse species.

  5. Effects of prolonged weightlessness on the swimming pattern of fish aboard Skylab 3

    NASA Technical Reports Server (NTRS)

    Von Baumgarten, R. J.; Simmonds, R. C.; Boyd, J. F.; Garriott, O. K.

    1975-01-01

    Looping behavior of minnows aboard Skylab 3 is analyzed. Extensive looping patterns were observed at first look on the third day of weightlessness; thereafter, the frequency of the looping episodes diminished until complete adaptation on the twenty-first day, at which time the fish oriented themselves with their backs to the light. The swimming anomaly could be due to (1) absence of continuous bending of sense hairs to a certain extent by gravity, causing the fish to tilt forward in an attempt to increase leverage on the hairs - in the absence of all gravity, tilting is continued into looping (this hypothesis is supported by parabolic flight experiments with partial gravity, in which only tilting was seen); or (2) an attempt by the fish to create a gravitoinertial stimulus by 'centrifuging' its otoliths by looping.

  6. Effects of prolonged weightlessness on the swimming pattern of fish aboard Skylab 3

    NASA Technical Reports Server (NTRS)

    Von Baumgarten, R. J.; Simmonds, R. C.; Boyd, J. F.; Garriott, O. K.

    1975-01-01

    Looping behavior of minnows aboard Skylab 3 is analyzed. Extensive looping patterns were observed at first look on the third day of weightlessness; thereafter, the frequency of the looping episodes diminished until complete adaptation on the twenty-first day, at which time the fish oriented themselves with their backs to the light. The swimming anomaly could be due to (1) absence of continuous bending of sense hairs to a certain extent by gravity, causing the fish to tilt forward in an attempt to increase leverage on the hairs - in the absence of all gravity, tilting is continued into looping (this hypothesis is supported by parabolic flight experiments with partial gravity, in which only tilting was seen); or (2) an attempt by the fish to create a gravitoinertial stimulus by 'centrifuging' its otoliths by looping.

  7. Riding the waves: the role of the body wave in undulatory fish swimming.

    PubMed

    Müller, Ulrike K; Stamhuis, Eize J; Videler, John J

    2002-11-01

    A continuously swimming mullet modulates its thrust production by changing slip-the ratio between its swimming speed U and the speed V with which the body wave travels down its body. This variation in thrust is reflected in the wake of the fish. We obtained 2-dimensional impressions of the wake behind a mullet swimming at a slip of 0.7 equivalent to active swimming, at a slip of 0.9 close to free-wheeling, and at a slip of 1.1 when the fish is braking. Independent of the slip, vortices are shed at the tail when the tail tip reaches its maximum lateral excursion. The manner in which the wake changes as it decays depends on the degree of slip: At a slip well below unity, the wake decays without any qualitative changes in shape, the medio-frontal cross section of the mature wake consists of a double row of alternating vortices separated by an undulating jet, and the angle between the jet flow and the mean path of motion is close to 45°; at a slip above unity, the vortices stretch out laterally and the mature wake resembles a single row of oval vortices with two vortex cores, and the jet between the vortices is almost perpendicular to the mean path of motion; the wake at slip of 0.9 exhibits a pattern intermediate between the wakes at slips 0.7 and 0.9 with slightly elongate vortices and a jet angle of 61°.

  8. Development of a Transient Acoustic Boundary Element Method to Predict the Noise Signature of Swimming Fish

    NASA Astrophysics Data System (ADS)

    Wagenhoffer, Nathan; Moored, Keith; Jaworski, Justin

    2015-11-01

    Animals have evolved flexible wings and fins to efficiently and quietly propel themselves through the air and water. The design of quiet and efficient bio-inspired propulsive concepts requires a rapid, unified computational framework that integrates three essential features: the fluid mechanics, the elastic structural response, and the noise generation. This study focuses on the development, validation, and demonstration of a transient, two-dimensional acoustic boundary element solver accelerated by a fast multipole algorithm. The resulting acoustic solver is used to characterize the acoustic signature produced by a vortex street advecting over a NACA 0012 airfoil, which is representative of vortex-body interactions that occur in schools of swimming fish. Both 2S and 2P canonical vortex streets generated by fish are investigated over the range of Strouhal number 0 . 2 < St < 0 . 4 , and the acoustic signature of the airfoil is quantified. This study provides the first estimate of the noise signature of a school of swimming fish. Lehigh University CORE Grant.

  9. Automatically detect and track multiple fish swimming in shallow water with frequent occlusion.

    PubMed

    Qian, Zhi-Ming; Cheng, Xi En; Chen, Yan Qiu

    2014-01-01

    Due to its universality, swarm behavior in nature attracts much attention of scientists from many fields. Fish schools are examples of biological communities that demonstrate swarm behavior. The detection and tracking of fish in a school are of important significance for the quantitative research on swarm behavior. However, different from other biological communities, there are three problems in the detection and tracking of fish school, that is, variable appearances, complex motion and frequent occlusion. To solve these problems, we propose an effective method of fish detection and tracking. In this method, first, the fish head region is positioned through extremum detection and ellipse fitting; second, The Kalman filtering and feature matching are used to track the target in complex motion; finally, according to the feature information obtained by the detection and tracking, the tracking problems caused by frequent occlusion are processed through trajectory linking. We apply this method to track swimming fish school of different densities. The experimental results show that the proposed method is both accurate and reliable.

  10. Evaluation of swimming performance for fish passage of longnose dace Rhinichthys cataractae using an experimental flume.

    PubMed

    Dockery, D R; McMahon, T E; Kappenman, K M; Blank, M

    2017-03-01

    The swimming performance of longnose dace Rhinichthys cataractae, the most widely distributed minnow (Cyprinidae) in North America, was assessed in relation to potential passage barriers. The study estimated passage success, maximum ascent distances and maximum sprint speed in an open-channel flume over a range of water velocities and temperatures (10·7, 15·3 and 19·3° C). Rhinichthys cataractae had high passage success (95%) in a 9·2 m flume section at mean test velocities of 39 and 64 cm s(-1) , but success rate dropped to 66% at 78 cm s(-1) . Only 20% of fish were able to ascend a 2·7 m section with a mean velocity of 122 cm s(-1) . Rhinichthys cataractae actively selected low-velocity pathways located along the bottom and corners of the flume at all test velocities and adopted position-holding behaviour at higher water velocities. Mean volitional sprint speed was 174 cm s(-1) when fish volitionally sprinted in areas of high water velocities. Swimming performance generally increased with water temperature and fish length. Based on these results, fishways with mean velocities <64 cm s(-1) should allow passage of most R. cataractae. Water velocities >100 cm s(-1) within structures should be limited to short distance (<1 m) and structures with velocities ≥158 cm s(-1) would probably represent movement barriers. Study results highlighted the advantages of evaluating a multitude of swimming performance metrics in an open-channel flume, which can simulate the hydraulic features of fishways and allow for behavioural observations that can facilitate the design of effective passage structures. © 2016 The Fisheries Society of the British Isles.

  11. Prediction of fish body's passive visco-elastic properties and related muscle mechanical performance in vivo during steady swimming

    NASA Astrophysics Data System (ADS)

    Zhang, Wei; Yu, YongLiang; Tong, BingGang

    2014-01-01

    For attaining the optimized locomotory performance of swimming fishes, both the passive visco-elastic properties of the fish body and the mechanical behavior of the active muscles should coordinate with the fish body's undulatory motion pattern. However, it is difficult to directly measure the visco-elastic constitutive relation and the muscular mechanical performance in vivo. In the present paper, a new approach based on the continuous beam model for steady swimming fish is proposed to predict the fish body's visco-elastic properties and the related muscle mechanical behavior in vivo. Given the lateral travelling-wave-like movement as the input condition, the required muscle force and the energy consumption are functions of the fish body's visco-elastic parameters, i.e. the Young's modulus E and the viscosity coefficient µ in the Kelvin model. After investigating the variations of the propagating speed of the required muscle force with the fish body's visco-elastic parameters, we analyze the impacts of the visco-elastic properties on the energy efficiencies, including the energy utilization ratios of each element of the kinematic chain in fish swimming and the overall efficiency. Under the constraints of reasonable wave speed of muscle activation and the physiological feasibility, the optimal design of the passive visco-elastic properties can be predicted aiming at maximizing the overall efficiency. The analysis is based on the small-amplitude steady swimming of the carangiform swimmer, with typical Reynolds number varying from 2.5×104 to 2.5×105, and the present results show that the non-dimensional Young's modulus is 112±34, and the non-dimensional viscosity coefficient is 13 approximately. In the present estimated ranges, the overall efficiency of the swimming fish is insensitive to the viscosity, and its magnitude is about 0.11±0.02, in the predicted range given by previous study.

  12. Scaling in Free-Swimming Fish and Implications for Measuring Size-at-Time in the Wild

    PubMed Central

    Broell, Franziska; Taggart, Christopher T.

    2015-01-01

    This study was motivated by the need to measure size-at-age, and thus growth rate, in fish in the wild. We postulated that this could be achieved using accelerometer tags based first on early isometric scaling models that hypothesize that similar animals should move at the same speed with a stroke frequency that scales with length-1, and second on observations that the speed of primarily air-breathing free-swimming animals, presumably swimming ‘efficiently’, is independent of size, confirming that stroke frequency scales as length-1. However, such scaling relations between size and swimming parameters for fish remain mostly theoretical. Based on free-swimming saithe and sturgeon tagged with accelerometers, we introduce a species-specific scaling relationship between dominant tail beat frequency (TBF) and fork length. Dominant TBF was proportional to length-1 (r2 = 0.73, n = 40), and estimated swimming speed within species was independent of length. Similar scaling relations accrued in relation to body mass-0.29. We demonstrate that the dominant TBF can be used to estimate size-at-time and that accelerometer tags with onboard processing may be able to provide size-at-time estimates among free-swimming fish and thus the estimation of growth rate (change in size-at-time) in the wild. PMID:26673777

  13. Scaling in Free-Swimming Fish and Implications for Measuring Size-at-Time in the Wild.

    PubMed

    Broell, Franziska; Taggart, Christopher T

    2015-01-01

    This study was motivated by the need to measure size-at-age, and thus growth rate, in fish in the wild. We postulated that this could be achieved using accelerometer tags based first on early isometric scaling models that hypothesize that similar animals should move at the same speed with a stroke frequency that scales with length-1, and second on observations that the speed of primarily air-breathing free-swimming animals, presumably swimming 'efficiently', is independent of size, confirming that stroke frequency scales as length-1. However, such scaling relations between size and swimming parameters for fish remain mostly theoretical. Based on free-swimming saithe and sturgeon tagged with accelerometers, we introduce a species-specific scaling relationship between dominant tail beat frequency (TBF) and fork length. Dominant TBF was proportional to length-1 (r2 = 0.73, n = 40), and estimated swimming speed within species was independent of length. Similar scaling relations accrued in relation to body mass-0.29. We demonstrate that the dominant TBF can be used to estimate size-at-time and that accelerometer tags with onboard processing may be able to provide size-at-time estimates among free-swimming fish and thus the estimation of growth rate (change in size-at-time) in the wild.

  14. Evaluation of a new coded electromyogram transmitter for studying swimming behavior and energetics in free-ranging fish

    SciTech Connect

    Brown, Richard S.; Tatara, Chris P.; Stephenson, John R.; Berejikian, Barry A.

    2007-06-25

    A new coded electromyogram (CEMG) transmitter was recently introduced to the market to allow broader application and greater flexibility of configurations. CEMG transmitters were implanted into twenty steelhead (Oncorhynchus mykiss) and calibrated to swimming speed in a respirometer. Linear regression models showed a strong positive relationship between output from CEMG transmitters and swimming speed. However, when signals from multiple transmitters were grouped, the relationship between CEMG output and swimming speed was less accurate than if signals from individual transmitters were used. The results, therefore, do not suggest that the CEMG transmitters acted similarly in all fish. Calibration data from one transmitter was not readily transferable among multiple fish implanted with the same transmitter, suggesting that the same transmitter implanted in multiple fish also performed dissimilarly. Variation in fish length, fish weight, location of transmitter implantation (distance from snout), and distance between the electrode tips did not account for the variation in models. Transmitters also had a relatively small working range of output at the swimming speeds tested. Nevertheless, new CEMG transmitters appear to have improved capabilities and should allow researchers to examine the locomotory behavior and energetics of smaller fish than previously possible with greater ease and less expense.

  15. Effects of non-uniform stiffness on the swimming performance of a passively-flexing, fish-like foil model.

    PubMed

    Lucas, Kelsey N; Thornycroft, Patrick J M; Gemmell, Brad J; Colin, Sean P; Costello, John H; Lauder, George V

    2015-10-08

    Simple mechanical models emulating fish have been used recently to enable targeted study of individual factors contributing to swimming locomotion without the confounding complexity of the whole fish body. Yet, unlike these uniform models, the fish body is notable for its non-uniform material properties. In particular, flexural stiffness decreases along the fish's anterior-posterior axis. To identify the role of non-uniform bending stiffness during fish-like propulsion, we studied four foil model configurations made by adhering layers of plastic sheets to produce discrete regions of high (5.5 × 10(-5) Nm(2)) and low (1.9 × 10(-5) Nm(2)) flexural stiffness of biologically-relevant magnitudes. This resulted in two uniform control foils and two foils with anterior regions of high stiffness and posterior regions of low stiffness. With a mechanical flapping foil controller, we measured forces and torques in three directions and quantified swimming performance under both heaving (no pitch) and constant 0° angle of attack programs. Foils self-propelled at Reynolds number 21 000-115 000 and Strouhal number ∼0.20-0.25, values characteristic of fish locomotion. Although previous models have emphasized uniform distributions and heaving motions, the combination of non-uniform stiffness distributions and 0° angle of attack pitching program was better able to reproduce the kinematics of freely-swimming fish. This combination was likewise crucial in maximizing swimming performance and resulted in high self-propelled speeds at low costs of transport and large thrust coefficients at relatively high efficiency. Because these metrics were not all maximized together, selection of the 'best' stiffness distribution will depend on actuation constraints and performance goals. These improved models enable more detailed, accurate analyses of fish-like swimming.

  16. Long-term Behavioral Tracking of Freely Swimming Weakly Electric Fish

    PubMed Central

    Jun, James J.; Longtin, André; Maler, Leonard

    2014-01-01

    Long-term behavioral tracking can capture and quantify natural animal behaviors, including those occurring infrequently. Behaviors such as exploration and social interactions can be best studied by observing unrestrained, freely behaving animals. Weakly electric fish (WEF) display readily observable exploratory and social behaviors by emitting electric organ discharge (EOD). Here, we describe three effective techniques to synchronously measure the EOD, body position, and posture of a free-swimming WEF for an extended period of time. First, we describe the construction of an experimental tank inside of an isolation chamber designed to block external sources of sensory stimuli such as light, sound, and vibration. The aquarium was partitioned to accommodate four test specimens, and automated gates remotely control the animals' access to the central arena. Second, we describe a precise and reliable real-time EOD timing measurement method from freely swimming WEF. Signal distortions caused by the animal's body movements are corrected by spatial averaging and temporal processing stages. Third, we describe an underwater near-infrared imaging setup to observe unperturbed nocturnal animal behaviors. Infrared light pulses were used to synchronize the timing between the video and the physiological signal over a long recording duration. Our automated tracking software measures the animal's body position and posture reliably in an aquatic scene. In combination, these techniques enable long term observation of spontaneous behavior of freely swimming weakly electric fish in a reliable and precise manner. We believe our method can be similarly applied to the study of other aquatic animals by relating their physiological signals with exploratory or social behaviors. PMID:24637642

  17. Deep RNA Sequencing of the Skeletal Muscle Transcriptome in Swimming Fish

    PubMed Central

    Palstra, Arjan P.; Beltran, Sergi; Burgerhout, Erik; Brittijn, Sebastiaan A.; Magnoni, Leonardo J.; Henkel, Christiaan V.; Jansen, Hans J.; van den Thillart, Guido E. E. J. M.; Spaink, Herman P.; Planas, Josep V.

    2013-01-01

    Deep RNA sequencing (RNA-seq) was performed to provide an in-depth view of the transcriptome of red and white skeletal muscle of exercised and non-exercised rainbow trout (Oncorhynchus mykiss) with the specific objective to identify expressed genes and quantify the transcriptomic effects of swimming-induced exercise. Pubertal autumn-spawning seawater-raised female rainbow trout were rested (n = 10) or swum (n = 10) for 1176 km at 0.75 body-lengths per second in a 6,000-L swim-flume under reproductive conditions for 40 days. Red and white muscle RNA of exercised and non-exercised fish (4 lanes) was sequenced and resulted in 15–17 million reads per lane that, after de novo assembly, yielded 149,159 red and 118,572 white muscle contigs. Most contigs were annotated using an iterative homology search strategy against salmonid ESTs, the zebrafish Danio rerio genome and general Metazoan genes. When selecting for large contigs (>500 nucleotides), a number of novel rainbow trout gene sequences were identified in this study: 1,085 and 1,228 novel gene sequences for red and white muscle, respectively, which included a number of important molecules for skeletal muscle function. Transcriptomic analysis revealed that sustained swimming increased transcriptional activity in skeletal muscle and specifically an up-regulation of genes involved in muscle growth and developmental processes in white muscle. The unique collection of transcripts will contribute to our understanding of red and white muscle physiology, specifically during the long-term reproductive migration of salmonids. PMID:23308156

  18. Three-dimensional numerical simulation of hydrodynamic interactions between pectoral-fin vortices and body undulation in a swimming fish

    NASA Astrophysics Data System (ADS)

    Yu, Cheng-Lun; Ting, Shang-Chieh; Yeh, Meng-Kao; Yang, Jing-Tang

    2011-09-01

    We investigated numerically the hydrodynamic interactions between pectoral-fin vortices and body undulation in a fish swimming with carangiform locomotion at a Reynolds number of 3.3 × 104; the three-dimensional, viscous, incompressible, Navier-Stokes equations were solved with a finite-volume method. For a fish swimming with the pectoral fins abducted, we characterized the wake flow structures, forces, and power consumption with respect to various Strouhal numbers. The numerical results reveal that a pair of vortices is formed immediately behind the abducted pectoral fins of a swimming fish. There exist hydrodynamic interactions between the pectoral-fin vortices and the undulating fish body. For Strouhal numbers in a range 0.2-0.8, the body undulation impedes the shedding of pectoral-fin vortices, resulting in vortices closely attached to the pectoral fins. In contrast, for Strouhal number = 0.1, the pectoral-fin vortices are shed from the pectoral fins and drift downstream. The low-pressure suction forces arising from the shed pectoral-fin vortices facilitate lateral movements of the fish body, decreasing the power consumption. This phenomenon indicates the possibility for an actual fish to harvest energy from the shed pectoral-fin vortices.

  19. Collective Response of Zebrafish Shoals to a Free-Swimming Robotic Fish

    PubMed Central

    Butail, Sachit; Bartolini, Tiziana; Porfiri, Maurizio

    2013-01-01

    In this work, we explore the feasibility of regulating the collective behavior of zebrafish with a free-swimming robotic fish. The visual cues elicited by the robot are inspired by salient features of attraction in zebrafish and include enhanced coloration, aspect ratio of a fertile female, and carangiform/subcarangiform locomotion. The robot is autonomously controlled with an online multi-target tracking system and swims in circular trajectories in the presence of groups of zebrafish. We investigate the collective response of zebrafish to changes in robot speed, achieved by varying its tail-beat frequency. Our results show that the speed of the robot is a determinant of group cohesion, quantified through zebrafish nearest-neighbor distance, which increases with the speed of the robot until it reaches . We also find that the presence of the robot causes a significant decrease in the group speed, which is not accompanied by an increase in the freezing response of the subjects. Findings of this study are expected to inform the design of experimental protocols that leverage the use of robots to study the zebrafish animal model. PMID:24146825

  20. Collective response of zebrafish shoals to a free-swimming robotic fish.

    PubMed

    Butail, Sachit; Bartolini, Tiziana; Porfiri, Maurizio

    2013-01-01

    In this work, we explore the feasibility of regulating the collective behavior of zebrafish with a free-swimming robotic fish. The visual cues elicited by the robot are inspired by salient features of attraction in zebrafish and include enhanced coloration, aspect ratio of a fertile female, and carangiform/subcarangiform locomotion. The robot is autonomously controlled with an online multi-target tracking system and swims in circular trajectories in the presence of groups of zebrafish. We investigate the collective response of zebrafish to changes in robot speed, achieved by varying its tail-beat frequency. Our results show that the speed of the robot is a determinant of group cohesion, quantified through zebrafish nearest-neighbor distance, which increases with the speed of the robot until it reaches [Formula: see text]. We also find that the presence of the robot causes a significant decrease in the group speed, which is not accompanied by an increase in the freezing response of the subjects. Findings of this study are expected to inform the design of experimental protocols that leverage the use of robots to study the zebrafish animal model.

  1. Activity Counts: The Effect of Swimming Activity on Quantity Discrimination in Fish

    PubMed Central

    Gómez-Laplaza, Luis M.; Gerlai, Robert

    2012-01-01

    Human infants and non-human animals can discriminate the larger of two sets of discrete items. This quantity discrimination may be based upon the number of items, or upon non-numerical variables of the sets that co-vary with number. We have demonstrated that angelfish select the larger of two shoals of conspecifics without using inter-fish distance or space occupied by the stimuli as cues. However, density appeared to influence the choice between large shoals. Here, we examine the role of another non-numerical cue, swimming activity of the stimulus fish, in quantity discrimination by angelfish. To control this variable, we varied the water temperature of the stimulus aquaria or restricted the space occupied by each fish in the stimulus shoals. We used the previously successfully discriminated contrasts consisting of large (10 vs. 5) and small (3 vs. 2) shoals. We also studied whether more active or less active shoals are preferred in case of equally sized shoals (10 vs. 10, 5 vs. 5, and 3 vs. 3). When differences in stimulus fish activity were minimized by temperature manipulation we found angelfish to prefer the larger shoal in the 3 vs. 2 comparison, but not in the 10 vs. 5 comparison. When activity was controlled by space restriction, angelfish preferred the larger shoal in both numerical contrasts. These results imply that the overall activity level of the contrasted shoals is not a necessary condition for small shoals discrimination in angelfish. On the other hand, the results obtained for the large shoals, together with results obtained in the control treatments (equal numerical contrasts and differing activity levels), suggest that activity is a sufficient condition for discrimination when large shoals are involved. Further experiments are needed to evaluate the influence of other continuous variables, and to assess whether the mechanisms underlying performance are comparable to those suggested for other animals. PMID:23162518

  2. The origin and evolution of the surfactant system in fish: insights into the evolution of lungs and swim bladders.

    PubMed

    Daniels, Christopher B; Orgeig, Sandra; Sullivan, Lucy C; Ling, Nicholas; Bennett, Michael B; Schürch, Samuel; Val, Adalberto Luis; Brauner, Colin J

    2004-01-01

    Several times throughout their radiation fish have evolved either lungs or swim bladders as gas-holding structures. Lungs and swim bladders have different ontogenetic origins and can be used either for buoyancy or as an accessory respiratory organ. Therefore, the presence of air-filled bladders or lungs in different groups of fishes is an example of convergent evolution. We propose that air breathing could not occur without the presence of a surfactant system and suggest that this system may have originated in epithelial cells lining the pharynx. Here we present new data on the surfactant system in swim bladders of three teleost fish (the air-breathing pirarucu Arapaima gigas and tarpon Megalops cyprinoides and the non-air-breathing New Zealand snapper Pagrus auratus). We determined the presence of surfactant using biochemical, biophysical, and morphological analyses and determined homology using immunohistochemical analysis of the surfactant proteins (SPs). We relate the presence and structure of the surfactant system to those previously described in the swim bladders of another teleost, the goldfish, and those of the air-breathing organs of the other members of the Osteichthyes, the more primitive air-breathing Actinopterygii and the Sarcopterygii. Snapper and tarpon swim bladders are lined with squamous and cuboidal epithelial cells, respectively, containing membrane-bound lamellar bodies. Phosphatidylcholine dominates the phospholipid (PL) profile of lavage material from all fish analyzed to date. The presence of the characteristic surfactant lipids in pirarucu and tarpon, lamellar bodies in tarpon and snapper, SP-B in tarpon and pirarucu lavage, and SPs (A, B, and D) in swim bladder tissue of the tarpon provide strong evidence that the surfactant system of teleosts is homologous with that of other fish and of tetrapods. This study is the first demonstration of the presence of SP-D in the air-breathing organs of nonmammalian species and SP-B in actinopterygian

  3. Reduced-order model of fish-like swimming due to shedding of unsteady point vortices

    NASA Astrophysics Data System (ADS)

    Tallapragada, Phanindra

    2013-11-01

    Reduced order models of biomimetic swimming in an ideal fluid, relying on the shedding of point vortices at short intervals of time, are useful to illuminate the essential underlying dynamics of locomotion in fluids. However these reduced order models still possess a state space that is very high dimensional, thus presenting challenges to develop control algorithms. A two-dimensional model that fully couples the motion of the solid boundary and the fluid containing singular distributions of vorticity is presented. The model relies on the shedding of unsteady point vortices, from the tip of a fish-like hydrofoil, in place of many steady point vortices. The subsequent reduction in the dimension of the state space makes the model more amenable to control algorithms. A simple case of the heading-angle control of a fish-like body will be illustrated. The model also has the advantage of being computationally significantly less demanding. More interestingly from a theoretical point of view, the reduced order model illustrates the connection between vortex shedding and velocity constraints encountered in rigid body mechanics.

  4. Water flow and fin shape polymorphism in coral reef fishes.

    PubMed

    Binning, Sandra A; Roche, Dominique G

    2015-03-01

    Water flow gradients have been linked to phenotypic differences and swimming performance across a variety of fish assemblages. However, the extent to which water motion shapes patterns of phenotypic divergence within species remains unknown. We tested the generality of the functional relationship between swimming morphology and water flow by exploring the extent of fin and body shape polymorphism in 12 widespread species from three families (Acanthuridae, Labridae, Pomacentridae) of pectoral-fin swimming (labriform) fishes living across localized wave exposure gradients. The pectoral fin shape of Labridae and Acanthuridae species was strongly related to wave exposure: individuals with more tapered, higher aspect ratio (AR) fins were found on windward reef crests, whereas individuals with rounder, lower AR fins were found on leeward, sheltered reefs. Three of seven Pomacentridae species showed similar trends, and pectoral fin shape was also strongly related to wave exposure in pomacentrids when fin aspect ratios of three species were compared across flow habitats at very small spatial scales (<100 m) along a reef profile (reef slope, crest, and back lagoon). Unlike fin shape, there were no intraspecific differences in fish body fineless ratio across habitats or depths. Contrary to our predictions, there was no pattern relating species' abundances to polymorphism across habitats (i.e., abundance was not higher at sites where morphology is better adapted to the environment). This suggests that there are behavioral and/or physiological mechanisms enabling some species to persist across flow habitats in the absence of morphological differences. We suggest that functional relationships between swimming morphology and water flow not only structure species assemblages, but are yet another important variable contributing to phenotypic differences within species. The close links between fin shape polymorphism and local water flow conditions appear to be important for

  5. Anthropogenic chemical cues can alter the swimming behaviour of juvenile stages of a temperate fish.

    PubMed

    Díaz-Gil, Carlos; Cotgrove, Lucy; Smee, Sarah Louise; Simón-Otegui, David; Hinz, Hilmar; Grau, Amalia; Palmer, Miquel; Catalán, Ignacio A

    2017-04-01

    Human pressure on coastal areas is affecting essential ecosystems including fish nursery habitats. Among these anthropogenic uses, the seasonal increment in the pressure due to leisure activities such as coastal tourism and yachting is an important environmental stressor in many coastal zones. These pressures may elicit understudied impacts due to, for example, sunscreens or other seasonal pollutants. The island of Majorca, northwest Mediterranean Sea, experiences one of the highest number of tourist visits per capita in the world, thus the surrounding coastal habitat is subject to high anthropogenic seasonal stress. Studies on early stages of fishes have observed responses to coastal chemical cues for the selection or avoidance of habitats. However, the potential interferences of human impacts on these signals are largely unknown. A choice chamber was used to determine water type preference and behaviour in naïve settled juvenile gilt-head sea bream (Sparus aurata), a temperate species of commercial interest. Fish were tested individually for behavioural changes with respect to water types from potential beneficial habitats, such as seawater with extract of the endemic seagrass Posidonia oceanica, anthropogenically influenced habitats such as water extracted from a commercial and recreational harbour and seawater mixed with sunscreen at concentrations observed in coastal waters. Using a Bayesian approach, we investigated a) water type preference; b) mean speed; and c) variance in the movement (as an indicator of burst swimming activity, or "sprint" behaviour) as behavioural descriptors with respect to water type. Fish spent similar percentage of time in treatment and control water types. However, movement descriptors showed that fish in sunscreen water moved slower (98.43% probability of being slower) and performed fewer sprints (90.1% probability of having less burst in speed) compared to control water. Less evident increases in sprints were observed in harbour

  6. Maximum sustainable speed, energetics and swimming kinematics of a tropical carangid fish, the green jack Caranx caballus.

    PubMed

    Dickson, K A; Donley, J M; Hansen, M W; Peters, J A

    2012-06-01

    Maximum sustained swimming speeds, swimming energetics and swimming kinematics were measured in the green jack Caranx caballus (Teleostei: Carangidae) using a 41 l temperature-controlled, Brett-type swimming-tunnel respirometer. In individual C. caballus [mean ±s.d. of 22·1 ± 2·2 cm fork length (L(F) ), 190 ± 61 g, n = 11] at 27·2 ± 0·7° C, mean critical speed (U(crit)) was 102·5 ± 13·7 cm s⁻¹ or 4·6 ± 0·9 L(F) s⁻¹. The maximum speed that was maintained for a 30 min period while swimming steadily using the slow, oxidative locomotor muscle (U(max,c)) was 99·4 ± 14·4 cm s⁻¹ or 4·5 ± 0·9 L(F) s⁻¹. Oxygen consumption rate (M in mg O₂ min⁻¹) increased with swimming speed and with fish mass, but mass-specific M (mg O₂ kg⁻¹ h⁻¹) as a function of relative speed (L(F) s⁻¹) did not vary significantly with fish size. Mean standard metabolic rate (R(S) ) was 170 ± 38 mg O₂ kg⁻¹ h⁻¹, and the mean ratio of M at U(max,c) to R(S) , an estimate of factorial aerobic scope, was 3·6 ± 1·0. The optimal speed (U(opt) ), at which the gross cost of transport was a minimum of 2·14 J kg⁻¹ m⁻¹, was 3·8 L(F) s⁻¹. In a subset of the fish studied (19·7-22·7 cm L(F) , 106-164 g, n = 5), the swimming kinematic variables of tailbeat frequency, yaw and stride length all increased significantly with swimming speed but not fish size, whereas tailbeat amplitude varied significantly with speed, fish mass and L(F) . The mean propulsive wavelength was 86·7 ± 5·6 %L(F) or 73·7 ± 5·2 %L(T) . Mean ±s.d. yaw and tailbeat amplitude values, calculated from lateral displacement of each intervertebral joint during a complete tailbeat cycle in three C. caballus (19·7, 21·6 and 22·7 cm L(F) ; 23·4, 25·3 and 26·4 cm L(T) ), were 4·6 ± 0·1 and 17·1 ± 2·2 %L(T) , respectively. Overall, the sustained swimming performance, energetics, kinematics, lateral displacement and intervertebral bending angles measured in C. caballus

  7. Embryogenesis and swimming behavior of Medaka fish in JUSTSAP STARS Program (STS-107).

    PubMed

    Niihori, Maki; Mogami, Yoshihiro; Naruse, Kiyoshi; Baba, Shoji A

    2003-10-01

    JUSTSAP (Japan-US Science, Technology and Space Application Program) Medaka fish experiment was carried out as a part of STARS (Space Technology and Research for Student) experiment, a space shuttle mission, STS-107 in January 2003. Four eggs laid on earth under artificially controlled environment were put in a closed ecological system, AHAB (Aquatic Habitat), and launched by Space Shuttle Columbia. For the control experiment, four eggs were put in the AHAB and remained on the ground. There was no remarkable difference in the time course of the development. In ground experiment embryos were observed to rotate in the egg membrane, whereas in flight unit they did not rotate. One egg hatched out on L (Launch) +8 days in flight unit. Four eggs hatched out in ground unit. Fry in flight unit was observed to face its back usually to the camera with little swimming movement. Fry in ground unit were observed to move actively and also to control their posture with respect to gravity vector.

  8. Sublethal effects of mosquito larvicides on swimming performance of larvivorous fish Melanotaenia duboulayi (Atheriniformes: Melanotaeniidae).

    PubMed

    Hurst, T P; Kay, B H; Ryan, P A; Brown, M D

    2007-02-01

    Laboratory studies were conducted to determine the sublethal effects of exposure to selected larvicides on the critical swimming speed (Ucrit) of crimson-spotted rainbowfish, Melanotaenia duboulayi (Castlenau). This native fish is common throughout southeastern Queensland, and it is increasingly being distributed as a biological control agent of mosquitoes. The selected larvicides included, two organophosphate (OP) compounds (temephos and pirimiphos-methyl), two microbial larvicides (Bacillus thuringiensis spp. israelensis [Bti] de Barjac and Bacillus sphaericus [Bs] Neide), and an insect growth regulator (IGR) (s-methoprene). Exposure to the OP temephos at 10 times the effective field concentration (EFC; 0.33 mg/liter), and OP pirimiphos-methyl at the EFC (0.50 mg/liter), resulted in a significant reduction in the Ucrit of M. duboulayi under controlled conditions. Conversely, exposure to the microbial (Bti and Bs) and IGR (s-methoprene) larvicides at 10 times the EFC had no effect on the Ucrit of M. duboulayi. Accordingly, these products are suitable for integrated pest management programs in Australia.

  9. Optimal undulatory swimming for a single fish-like body and for a pair of interacting swimmers

    NASA Astrophysics Data System (ADS)

    Maertens, Audrey P.; Gao, Amy; Triantafyllou, Michael S.

    2017-02-01

    We establish through numerical simulation conditions for optimal undulatory propulsion for a single fish, and for a pair of hydrodynamically interacting fish, accounting for linear and angular recoil. We first employ systematic 2D simulations to identify conditions for minimal propulsive power of a self-propelled fish, and continue with targeted 3D simulations for a danio-like fish. We find that the Strouhal number, phase angle between heave and pitch at the trailing edge, and angle of attack are principal parameters. Angular recoil has significant impact on efficiency, while optimized body bending requires maximum bending amplitude upstream of the trailing edge. For 2D simulations, imposing a deformation based on measured displacement for carangiform swimming provides efficiency of 40%, which increases for an optimized profile to 57%; for a 3D fish, the corresponding increase is from 22% to 35%; all at Reynolds number 5000. Next, we turn to 2D simulation of two hydrodynamically interacting fish. We find that the upstream fish benefits energetically only for small distances. In contrast, the downstream fish can benefit at any position that allows interaction with the upstream wake, provided its body motion is timed appropriately with respect to the oncoming vortices. For an in-line configuration, one body length apart, the optimal efficiency of the downstream fish can increase to 66%; for an offset arrangement it can reach 81%. This proves that in groups of fish, energy savings can be achieved for downstream fish through interaction with oncoming vortices, even when the downstream fish lies directly inside the jet-like flow of an upstream fish.

  10. Sustained impairment of respiratory function and swim performance following acute oil exposure in a coastal marine fish.

    PubMed

    Johansen, J L; Esbaugh, A J

    2017-06-01

    Acute exposure to crude oil polycyclic aromatic hydrocarbons (PAH) can severely impair cardiorespiratory function and swim performance of larval fish; however, the effects of acute oil exposure on later life stages and the capacity for subsequent recovery is less clear. Red drum (Sciaenops ocellatus) is an economically important apex predator native to the Gulf of Mexico, which was directly exposed to the 2010 Deep Water Horizon (DWH) oil spill. Here we examine impact and recovery of young adult red drum from exposure to concentrations of 0, 4.1, and 12.1μgL(-1) ΣPAH50 naturally weathered oil-water accommodated fractions (geometric mean), which are well within the range of concentrations measured during the DWH incident. We focused on aerobic scope (ASc), burst- and critical swimming speeds (Uburst and Ucrit), cost of transport (COT), as well as the capacity to repay oxygen debt following exhaustive exercise (EPOC), which are critical parameters for success of all life stages of fishes. A 24h acute exposure to 4.1μgL(-1) ΣPAH caused a significant 9.7 and 12.6% reduction of Uburst and Ucrit respectively, but no change in ASc, COT or EPOC, highlighting a decoupled effect on the respiratory and swimming systems. A higher exposure concentration, 12.1μgL(-1) ΣPAH, caused an 8.6 and 8.4% impairment of Uburst and Ucrit, as well as an 18.4% reduction in ASc. These impairments persisted six weeks post-exposure, suggesting that recorded impacts are entrenched. Large predatory fishes are critically dependent on the cardiorespiratory and swimming systems for ecological fitness, and long-term impairment of performance due to acute oil exposure suggests that even acute exposure events may have long lasting impacts on the ecological fitness of affected populations. Copyright © 2017. Published by Elsevier B.V.

  11. Spiral swimming behavior due to cranial and vertebral lesions associated with Cytophaga psychrophila infections in salmonid fishes

    USGS Publications Warehouse

    Kent, M.L.; Groff, J.M.; Morrison, J.K.; Yasutake, W.T.; Holt, R.A.

    1989-01-01

    C. psychrophila infections of the cranium and anterior vertebrae in salmonid fishes were associated with ataxia, spiral swimming along the axis of the fish, and death. The syndrome was observed in 2-10% of underyearling coho salmon Oncorhynchus kisutch, rainbow troutSalmo gairdneri, and steelhead trout S. gairdneri at several private, state, and federal hatcheries in Washington and Oregon, USA, between 1963 and 1987. Affected fish did not recover and ultimately died. Histological examination consistently revealed subacute to chronic periostitis, osteitis, meningitis, and ganglioneuritis. Inflammation and periosteal proliferation of the anterior vertebrae at the junction of the vertebral column with the cranium with extension into the cranial case was a consistent feature. The adjacent nervous tissue, particularly the medulla, was often compressed by the proliferative lesion, and this may have caused the ataxia. Though bacteria were seldom observed in these lesions. C. psychrophilawas isolated in culture from the cranial cavity of all affected fish that were tested. Epidemiological observations suggested that this bacterium is the causative agent because the spiral swimming behaviour and lesions were observed only in populations that had recovered from acute C. psychrophila infections.

  12. The Inner Ear and its Coupling to the Swim Bladder in the Deep-Sea Fish Antimora rostrata (Teleostei: Moridae)

    PubMed Central

    Deng, Xiaohong; Wagner, Hans-Joachim; Popper, Arthur N.

    2011-01-01

    The inner ear structure of Antimora rostrata and its coupling to the swim bladder were analyzed and compared with the inner ears of several shallow-water species that also have similar coupling. The inner ear of Antimora has a long saccular otolith and sensory epithelium as compared to many other fishes. Some parts of the membranous labyrinth are thick and rigid, while other parts are thinner but attached tightly to the bony capsule. The partially rigid membranous labyrinth, along with its intimate connection to the swim bladder, may help the inner ear follow the sound oscillations from the swim bladder with better precision than would occur in a less rigid inner ear. In addition, the saccular sensory epithelium has an elaborate structure and an anterior enlargement that may be correlated with increased hearing sensitivity. Some of the features in the inner ear of Antimora may reflect the functional specialization of deep-water living and support the hypothesis that there is enhanced inner ear sensitivity in some deep-sea fishes. PMID:21532967

  13. Quantifying Fish Swimming Behavior in Response to Acute Exposure of Aqueous Copper Using Computer Assisted Video and Digital Image Analysis

    PubMed Central

    Calfee, Robin D.; Puglis, Holly J.; Little, Edward E.; Brumbaugh, William G.; Mebane, Christopher A.

    2016-01-01

    Behavioral responses of aquatic organisms to environmental contaminants can be precursors of other effects such as survival, growth, or reproduction. However, these responses may be subtle, and measurement can be challenging. Using juvenile white sturgeon (Acipenser transmontanus) with copper exposures, this paper illustrates techniques used for quantifying behavioral responses using computer assisted video and digital image analysis. In previous studies severe impairments in swimming behavior were observed among early life stage white sturgeon during acute and chronic exposures to copper. Sturgeon behavior was rapidly impaired and to the extent that survival in the field would be jeopardized, as fish would be swept downstream, or readily captured by predators. The objectives of this investigation were to illustrate protocols to quantify swimming activity during a series of acute copper exposures to determine time to effect during early lifestage development, and to understand the significance of these responses relative to survival of these vulnerable early lifestage fish. With mortality being on a time continuum, determining when copper first affects swimming ability helps us to understand the implications for population level effects. The techniques used are readily adaptable to experimental designs with other organisms and stressors. PMID:26967350

  14. Quantifying fish swimming behavior in response to acute exposure of aqueous copper using computer assisted video and digital image analysis

    USGS Publications Warehouse

    Calfee, Robin D.; Puglis, Holly J.; Little, Edward E.; Brumbaugh, William G.; Mebane, Christopher A.

    2016-01-01

    Behavioral responses of aquatic organisms to environmental contaminants can be precursors of other effects such as survival, growth, or reproduction. However, these responses may be subtle, and measurement can be challenging. Using juvenile white sturgeon (Acipenser transmontanus) with copper exposures, this paper illustrates techniques used for quantifying behavioral responses using computer assisted video and digital image analysis. In previous studies severe impairments in swimming behavior were observed among early life stage white sturgeon during acute and chronic exposures to copper. Sturgeon behavior was rapidly impaired and to the extent that survival in the field would be jeopardized, as fish would be swept downstream, or readily captured by predators. The objectives of this investigation were to illustrate protocols to quantify swimming activity during a series of acute copper exposures to determine time to effect during early lifestage development, and to understand the significance of these responses relative to survival of these vulnerable early lifestage fish. With mortality being on a time continuum, determining when copper first affects swimming ability helps us to understand the implications for population level effects. The techniques used are readily adaptable to experimental designs with other organisms and stressors.

  15. Substrate roughening improves swimming performance in two small-bodied riverine fishes: implications for culvert remediation and design

    PubMed Central

    Rodgers, Essie M.; Heaslip, Breeana M.; Cramp, Rebecca L.; Riches, Marcus; Gordos, Matthew A.

    2017-01-01

    Abstract Worldwide declines in riverine fish abundance and diversity have been linked to the fragmentation of aquatic habitats through the installation of instream structures (e.g. culverts, dams, weirs and barrages). Restoring riverine connectivity can be achieved by remediating structures impeding fish movements by, for example, replacing smooth substrates of pipe culverts with naturalistic substrates (i.e. river stones; culvert roughening). However, empirical evaluations of the efficacy of such remediation efforts are often lacking despite the high economic cost. We assessed the effectiveness of substrate roughening in improving fish swimming performance and linked this to estimates of upstream passage success. Critical swimming speeds (Ucrit) of two small-bodied fish, purple-spotted gudgeon (Mogurnda adspersa; 7.7–11.6 cm total length, BL) and crimson-spotted rainbowfish (Melanotaenia duboulayi; 4.2–8.7 cm BL) were examined. Swimming trials were conducted in a hydraulic flume fitted with either a smooth acrylic substrate (control) or a rough substrate with fixed river stones. Swimming performance was improved on the rough compared to the smooth substrate, with Mo. adspersa (Ucrit-smooth = 0.28 ± 0.0 m s−1, 2.89 ± 0.1 BL s−1, Ucrit-rough = 0.36 ± 0.02 m s−1, 3.66 ± 0.22 BL s−1, mean ± s.e) and Me. duboulayi (Ucrit-smooth = 0.46 ± 0.01 m s−1, 7.79 ± 0.33 BL s−1; Ucrit-rough = = 0.55 ± 0.03 m s−1, 9.83 ± 0.67 BL s−1, mean ± s.e.) both experiencing a 26% increase in relative Ucrit. Traversable water velocity models predicted maximum water speeds allowing successful upstream passage of both species to substantially increase following roughening remediation. Together these findings suggest culvert roughening may be a solution which allows hydraulic efficiency goals to be met, without compromising fish passage. PMID:28567285

  16. Substrate roughening improves swimming performance in two small-bodied riverine fishes: implications for culvert remediation and design.

    PubMed

    Rodgers, Essie M; Heaslip, Breeana M; Cramp, Rebecca L; Riches, Marcus; Gordos, Matthew A; Franklin, Craig E

    2017-01-01

    Worldwide declines in riverine fish abundance and diversity have been linked to the fragmentation of aquatic habitats through the installation of instream structures (e.g. culverts, dams, weirs and barrages). Restoring riverine connectivity can be achieved by remediating structures impeding fish movements by, for example, replacing smooth substrates of pipe culverts with naturalistic substrates (i.e. river stones; culvert roughening). However, empirical evaluations of the efficacy of such remediation efforts are often lacking despite the high economic cost. We assessed the effectiveness of substrate roughening in improving fish swimming performance and linked this to estimates of upstream passage success. Critical swimming speeds (Ucrit) of two small-bodied fish, purple-spotted gudgeon (Mogurnda adspersa; 7.7-11.6 cm total length, BL) and crimson-spotted rainbowfish (Melanotaenia duboulayi; 4.2-8.7 cm BL) were examined. Swimming trials were conducted in a hydraulic flume fitted with either a smooth acrylic substrate (control) or a rough substrate with fixed river stones. Swimming performance was improved on the rough compared to the smooth substrate, with Mo. adspersa (Ucrit-smooth = 0.28 ± 0.0 m s(-1), 2.89 ± 0.1 BL s(-1), Ucrit-rough = 0.36 ± 0.02 m s(-1), 3.66 ± 0.22 BL s(-1), mean ± s.e) and Me. duboulayi (Ucrit-smooth = 0.46 ± 0.01 m s(-1), 7.79 ± 0.33 BL s(-1); Ucrit-rough = = 0.55 ± 0.03 m s(-1), 9.83 ± 0.67 BL s(-1), mean ± s.e.) both experiencing a 26% increase in relative Ucrit. Traversable water velocity models predicted maximum water speeds allowing successful upstream passage of both species to substantially increase following roughening remediation. Together these findings suggest culvert roughening may be a solution which allows hydraulic efficiency goals to be met, without compromising fish passage.

  17. Unveiling the neurotoxicity of methylmercury in fish (Diplodus sargus) through a regional morphometric analysis of brain and swimming behavior assessment.

    PubMed

    Puga, Sónia; Pereira, Patrícia; Pinto-Ribeiro, Filipa; O'Driscoll, Nelson J; Mann, Erin; Barata, Marisa; Pousão-Ferreira, Pedro; Canário, João; Almeida, Armando; Pacheco, Mário

    2016-11-01

    The current study aims to shed light on the neurotoxicity of MeHg in fish (white seabream - Diplodus sargus) by the combined assessment of: (i) MeHg toxicokinetics in the brain, (ii) brain morphometry (volume and number of neurons plus glial cells in specific brain regions) and (iii) fish swimming behavior (endpoints associated with the motor performance and the fear/anxiety-like status). Fish were surveyed for all the components after 7 (E7) and 14 (E14) days of dietary exposure to MeHg (8.7μgg(-1)), as well as after a post-exposure period of 28days (PE28). MeHg was accumulated in the brain of D. sargus after a short time (E7) and reached a maximum at the end of the exposure period (E14), suggesting an efficient transport of this toxicant into fish brain. Divalent inorganic Hg was also detected in fish brain along the experiment (indicating demethylation reactions), although levels were 100-200 times lower than MeHg, which pinpoints the organic counterpart as the great liable for the recorded effects. In this regard, a decreased number of cells in medial pallium and optic tectum, as well as an increased hypothalamic volume, occurred at E7. Such morphometric alterations were followed by an impairment of fish motor condition as evidenced by a decrease in the total swimming time, while the fear/anxiety-like status was not altered. Moreover, at E14 fish swam a greater distance, although no morphometric alterations were found in any of the brain areas, probably due to compensatory mechanisms. Additionally, although MeHg decreased almost two-fold in the brain during post-exposure, the levels were still high and led to a loss of cells in the optic tectum at PE28. This is an interesting result that highlights the optic tectum as particularly vulnerable to MeHg exposure in fish. Despite the morphometric alterations reported in the optic tectum at PE28, no significant changes were found in fish behavior. Globally, the effects of MeHg followed a multiphasic profile, where

  18. Entrainment, retention, and transport of freely swimming fish in junction gaps between commercial barges operating on the Illinois Waterway

    USGS Publications Warehouse

    Davis, Jeremiah J.; Jackson, P. Ryan; Engel, Frank; LeRoy, Jessica Z.; Neeley, Rebecca N.; Finney, Samuel T.; Murphy, Elizabeth A.

    2016-01-01

    Large Electric Dispersal Barriers were constructed in the Chicago Sanitary and Ship Canal (CSSC) to prevent the transfer of invasive fish species between the Mississippi River Basin and the Great Lakes Basin while simultaneously allowing the passage of commercial barge traffic. We investigated the potential for entrainment, retention, and transport of freely swimming fish within large gaps (> 50 m3) created at junction points between barges. Modified mark and capture trials were employed to assess fish entrainment, retention, and transport by barge tows. A multi-beam sonar system enabled estimation of fish abundance within barge junction gaps. Barges were also instrumented with acoustic Doppler velocity meters to map the velocity distribution in the water surrounding the barge and in the gap formed at the junction of two barges. Results indicate that the water inside the gap can move upstream with a barge tow at speeds near the barge tow travel speed. Water within 1 m to the side of the barge junction gaps was observed to move upstream with the barge tow. Observed transverse and vertical water velocities suggest pathways by which fish may potentially be entrained into barge junction gaps. Results of mark and capture trials provide direct evidence that small fish can become entrained by barges, retained within junction gaps, and transported over distances of at least 15.5 km. Fish entrained within the barge junction gap were retained in that space as the barge tow transited through locks and the Electric Dispersal Barriers, which would be expected to impede fish movement upstream.

  19. A numerical study of linear and nonlinear kinematic models in fish swimming with the DSD/SST method

    NASA Astrophysics Data System (ADS)

    Tian, Fang-Bao

    2015-03-01

    Flow over two fish (modeled by two flexible plates) in tandem arrangement is investigated by solving the incompressible Navier-Stokes equations numerically with the DSD/SST method to understand the differences between the geometrically linear and nonlinear models. In the simulation, the motions of the plates are reconstructed from a vertically flowing soap film tunnel experiment with linear and nonlinear kinematic models. Based on the simulations, the drag, lift, power consumption, vorticity and pressure fields are discussed in detail. It is found that the linear and nonlinear models are able to reasonably predict the forces and power consumption of a single plate in flow. Moreover, if multiple plates are considered, these two models yield totally different results, which implies that the nonlinear model should be used. The results presented in this work provide a guideline for future studies in fish swimming.

  20. Swimming performance of upstream migrant fishes in open-channel flow: A new approach to predicting passage through velocity barriers

    USGS Publications Warehouse

    Haro, A.; Castro-Santos, T.; Noreika, J.; Odeh, M.

    2004-01-01

    The ability to traverse barriers of high-velocity flow limits the distributions of many diadromous and other migratory fish species, yet very few data exist that quantify this ability. We provide a detailed analysis of sprint swimming ability of six migratory fish species (American shad (Alosa sapidissima), alewife (Alosa pseudoharengus), blueback herring (Alosa aestivalis), striped bass (Morone saxatilis), walleye (Stizostedion vitreum), and white sucker (Catostomus commersoni)) against controlled water velocities of 1.5-4.5 m??s-1 in a large, open-channel flume. Performance was strictly voluntary: no coercive incentives were used to motivate fish to sprint. We used these data to generate models of maximum distance traversed, taking into account effects of flow velocity, body length, and temperature. Although the maximum distance traversed decreased with increasing velocity, the magnitude of this effect varied among species. Other covariate effects were likewise variable, with divergent effects of temperature and nonuniform length effects. These effects do not account for all of the variability in performance, however, and behavioral traits may account for observed interspecific differences. We propose the models be used to develop criteria for fish passage structures, culverts, and breached dams.

  1. Passive elastic mechanism to mimic fish-muscle action in anguilliform swimming

    PubMed Central

    Ramananarivo, Sophie; Godoy-Diana, Ramiro; Thiria, Benjamin

    2013-01-01

    Swimmers in nature use body undulations to generate propulsive and manoeuvring forces. The anguilliform kinematics is driven by muscular actions all along the body, involving a complex temporal and spatial coordination of all the local actuations. Such swimming kinematics can be reproduced artificially, in a simpler way, by using the elasticity of the body passively. Here, we present experiments on self-propelled elastic swimmers at a free surface in the inertial regime. By addressing the fluid–structure interaction problem of anguilliform swimming, we show that our artificial swimmers are well described by coupling a beam theory with the potential flow model of Lighthill. In particular, we show that the propagative nature of the elastic wave producing the propulsive force is strongly dependent on the dissipation of energy along the body of the swimmer. PMID:23985737

  2. Three-dimensional reconstruction of the fast-start swimming kinematics of densely schooling fish

    PubMed Central

    Paley, Derek A.

    2012-01-01

    Information transmission via non-verbal cues such as a fright response can be quantified in a fish school by reconstructing individual fish motion in three dimensions. In this paper, we describe an automated tracking framework to reconstruct the full-body trajectories of densely schooling fish using two-dimensional silhouettes in multiple cameras. We model the shape of each fish as a series of elliptical cross sections along a flexible midline. We estimate the size of each ellipse using an iterated extended Kalman filter. The shape model is used in a model-based tracking framework in which simulated annealing is applied at each step to estimate the midline. Results are presented for eight fish with occlusions. The tracking system is currently being used to investigate fast-start behaviour of schooling fish in response to looming stimuli. PMID:21642367

  3. Three-dimensional reconstruction of the fast-start swimming kinematics of densely schooling fish.

    PubMed

    Butail, Sachit; Paley, Derek A

    2012-01-07

    Information transmission via non-verbal cues such as a fright response can be quantified in a fish school by reconstructing individual fish motion in three dimensions. In this paper, we describe an automated tracking framework to reconstruct the full-body trajectories of densely schooling fish using two-dimensional silhouettes in multiple cameras. We model the shape of each fish as a series of elliptical cross sections along a flexible midline. We estimate the size of each ellipse using an iterated extended Kalman filter. The shape model is used in a model-based tracking framework in which simulated annealing is applied at each step to estimate the midline. Results are presented for eight fish with occlusions. The tracking system is currently being used to investigate fast-start behaviour of schooling fish in response to looming stimuli.

  4. Effect of drying and frying conditions on physical and chemical characteristics of fish maw from swim bladder of seabass (Lates calcarifer).

    PubMed

    Sinthusamran, Sittichoke; Benjakul, Soottawat

    2015-12-01

    Swim bladder is generated as a by-product during evisceration. It has been used for the production of fish maw, in which several processing parameters determine the characteristics or quality of the resulting fish maw. The present study aimed to investigate the characteristics of fish maws from seabass swim bladder as influenced by drying and frying conditions. The expansion ratio and oil uptake content of fish maw increased as the moisture content of swim bladder increased (P < 0.05). Nevertheless, the expansion ratio of fish maw decreased when the moisture content was higher than 150 g kg(-1) . The L*-value decreased, whilst the a*- and b*-values of fish maw increased with increasing moisture content. When pre-frying and frying temperatures increased, the expansion ratio of fish maw increased (P < 0.05). However, the expansion ratio decreased when the frying was performed at a temperature higher than 200 °C. The oil uptake contents of fish maw with frying temperatures of 180 and 200 °C were in the range of 451.06-578.06 g kg(-1) , whereas the lower contents (378.60-417.17 g kg(-1) ) were found in those having frying temperatures of 220-240 °C. Hardness of fish maw decreased but no changes in fracturability were observed with increasing pre-frying temperature when subsequent frying was carried out 200 °C. Drying temperatures, moisture content, pre-frying and frying temperatures were the factors influencing the characteristics and properties of fish maws from seabass swim bladder. Fish maw could be prepared by pre-frying swim bladder, dried at 60 °C to obtain 150 g kg(-1) moisture content, at 110 °C for 5 min, followed by frying at 200 °C for 20 s. © 2014 Society of Chemical Industry.

  5. On inappropriately used neuronal circuits as a possible basis of the ``loop-swimming'' behaviour of fish under reduced gravity: a theoretical study

    NASA Astrophysics Data System (ADS)

    Anken, R. H.; Rahmann, H.

    One hypothesis for the explanation of the so-called ``loop-swimming'' behaviour in fish when being subjected to reduced gravity assumes that the activities of the differently weighted otoliths of the two labyrinths are well compensated on ground but that a functional asymmetry is induced in weightlessness, resulting in a tonus asymmetry of the body and by this generating the ``loop-swimming'' behaviour. The basis of this abnormal behaviour has to be searched for in the central nervous system (cns), where the signal-transduction from the inner ear- related signal internalisation to the signal response takes place. Circuits within the CNS of fish, that could possibly generate the ``loop-swimming'', might be as follows: An asymmetric activation of vestibulospinal circuits would directly result in a tonus asymmetry of the body. An asymmetric activation of the oculomotor nucleus would generate an asymmetrical rotation of the eyes. This would cause in its turn asymmetric images on the two retinas, which were forwarded to the diencephalic accessory optic system (AOS). It is the task of the AOS to stabilize retinal images, thereby involving the cerebellum, which is the main integration center for sensory and motor modalities. With this, the cerebellar output would generate a tonus asymmetry of the body in order to make the body of the fish follow its eyes. Such movements (especially when assuming an open loop control) would end up in the aforementioned ``loop-swimming'' behaviour.

  6. Bottles as models: predicting the effects of varying swimming speed and morphology on size selectivity and filtering efficiency in fishes.

    PubMed

    Paig-Tran, E W Misty; Bizzarro, Joseph J; Strother, James A; Summers, Adam P

    2011-05-15

    We created physical models based on the morphology of ram suspension-feeding fishes to better understand the roles morphology and swimming speed play in particle retention, size selectivity and filtration efficiency during feeding events. We varied the buccal length, flow speed and architecture of the gills slits, including the number, size, orientation and pore size/permeability, in our models. Models were placed in a recirculating flow tank with slightly negatively buoyant plankton-like particles (~20-2000 μm) collected at the simulated esophagus and gill rakers to locate the highest density of particle accumulation. Particles were captured through sieve filtration, direct interception and inertial impaction. Changing the number of gill slits resulted in a change in the filtration mechanism of particles from a bimodal filter, with very small (≤ 50 μm) and very large (>1000 μm) particles collected, to a filter that captured medium-sized particles (101-1000 μm). The number of particles collected on the gill rakers increased with flow speed and skewed the size distribution towards smaller particles (51-500 μm). Small pore sizes (105 and 200 μm mesh size) had the highest filtration efficiencies, presumably because sieve filtration played a significant role. We used our model to make predictions about the filtering capacity and efficiency of neonatal whale sharks. These results suggest that the filtration mechanics of suspension feeding are closely linked to an animal's swimming speed and the structural design of the buccal cavity and gill slits.

  7. A unique swim bladder-inner ear connection in a teleost fish revealed by a combined high-resolution microtomographic and three-dimensional histological study

    PubMed Central

    2013-01-01

    Background In most modern bony fishes (teleosts) hearing improvement is often correlated with a close morphological relationship between the swim bladder or other gas-filled cavities and the saccule or more rarely with the utricle. A connection of an accessory hearing structure to the third end organ, the lagena, has not yet been reported. A recent study in the Asian cichlid Etroplus maculatus provided the first evidence that a swim bladder may come close to the lagena. Our study was designed to uncover the swim bladder-inner ear relationship in this species. We used a new approach by applying a combination of two high-resolution techniques, namely microtomographic (microCT) imaging and histological serial semithin sectioning, providing the basis for subsequent three-dimensional reconstructions. Prior to the morphological study, we additionally measured auditory evoked potentials at four frequencies (0.5, 1, 2, 3 kHz) to test the hearing abilities of the fish. Results E. maculatus revealed a complex swim bladder-inner ear connection in which a bipartite swim bladder extension contacts the upper as well as the lower parts of each inner ear, a condition not observed in any other teleost species studied so far. The gas-filled part of the extension is connected to the lagena via a thin bony lamella and is firmly attached to this bony lamella with connective material. The second part of the extension, a pad-like structure, approaches the posterior and horizontal semicircular canals and a recessus located posterior to the utricle. Conclusions Our study is the first detailed report of a link between the swim bladder and the lagena in a teleost species. We suggest that the lagena has an auditory function in this species because the most intimate contact exists between the swim bladder and this end organ. The specialized attachment of the saccule to the cranial bone and the close proximity of the swim bladder extension to the recessus located posterior to the utricle

  8. Do swimming fish always grow fast? Investigating the magnitude and physiological basis of exercise-induced growth in juvenile New Zealand yellowtail kingfish, Seriola lalandi.

    PubMed

    Brown, Elliot J; Bruce, Michael; Pether, Steve; Herbert, Neill A

    2011-06-01

    There is a wealth of evidence showing that a moderate level of non-stop exercise improves the growth and feed conversion of many active fishes. A diverse number of active fish are currently being farmed, and an optimal level of exercise may feasibly improve the production efficiency of these species in intensive culture systems. Our experiments have set out to resolve the growth benefits of juvenile New Zealand yellowtail kingfish (Seriola lalandi) enforced to swim in currents at various speeds over two temperatures (14.9 and 21.1 °C). We also probed potential sources of physiological efficiency in an attempt to resolve how growth is enhanced at a time of high energetic expenditure. Results show that long-term exercise yields a 10% increase in growth but this occurs in surprisingly low flows (0.75 BL s⁻¹) and only under favourable environmental temperatures (21.1 °C). Experiments using a swim flume respirometer indicate that exercise training has no effect on metabolic scope or critical swimming speeds but it does improve swimming efficiency (lower gross costs of transport, GCOT). Such efficiency may potentially help reconcile the costs of growth and exercise within the range of available metabolic energy (scope). With growth boosted in surprisingly low flows and elevated water temperatures only, further investigations are required to understand the bioenergetics and partitioning of costs in the New Zealand yellowtail kingfish.

  9. Visual cues eliciting the feeding reaction of a planktivorous fish swimming in a current.

    PubMed

    Mussi, Martina; McFarland, William N; Domenici, Paolo

    2005-03-01

    The visual plankivorous feeding behaviour of the shiner perch (Cymatogaster aggregata) was investigated by means of a flow tank operated at various current speeds. Artemia salina was used as prey. In a second set of experiments, Artemia was darkened with black ink, to compare the visually mediated behaviour of C. aggregata while feeding on dark prey vs feeding on natural (i.e. semi-transparent) prey. The positions of the fish and its prey at the time of the feeding reaction of C. aggregata were measured in three dimensions. Prey were on average closer and more in line with the fish's axis when feeding reactions to darkened Artemia were considered, in comparison with natural Artemia. Three potential mechanisms triggering the feeding reaction of C. aggregata were explored: the prey may trigger a reaction in C. aggregata when it reaches a threshold (1) angular size, (2) angular velocity, or (3) rate of change of the angular size (i.e. loom) of the prey as it is carried passively by the current towards the fish. Our results show that angular velocity may trigger the fish's reaction when using semi-transparent prey, while loom may trigger the reaction to darkened prey. This suggests that feeding behaviour of planktivorous fish is flexible and can use different cues to trigger a motor reaction to prey with different visual characteristics. The feeding reaction appeared to occur at longer distances for semi-transparent rather than darkened Artemia. We suggest that semi-transparent Artemia were visible at greater distances because of their higher scattering (i.e. diffuse reflectance) that made them appear brighter when viewed against a dark background.

  10. Not all sharks are "swimming noses": variation in olfactory bulb size in cartilaginous fishes.

    PubMed

    Yopak, Kara E; Lisney, Thomas J; Collin, Shaun P

    2015-03-01

    Olfaction is a universal modality by which all animals sample chemical stimuli from their environment. In cartilaginous fishes, olfaction is critical for various survival tasks including localizing prey, avoiding predators, and chemosensory communication with conspecifics. Little is known, however, about interspecific variation in olfactory capability in these fishes, or whether the relative importance of olfaction in relation to other sensory systems varies with regard to ecological factors, such as habitat and lifestyle. In this study, we have addressed these questions by directly examining interspecific variation in the size of the olfactory bulbs (OB), the region of the brain that receives the primary sensory projections from the olfactory nerve, in 58 species of cartilaginous fishes. Relative OB size was compared among species occupying different ecological niches. Our results show that the OBs maintain a substantial level of allometric independence from the rest of the brain across cartilaginous fishes and that OB size is highly variable among species. These findings are supported by phylogenetic generalized least-squares models, which show that this variability is correlated with ecological niche, particularly habitat. The relatively largest OBs were found in pelagic-coastal/oceanic sharks, especially migratory species such as Carcharodon carcharias and Galeocerdo cuvier. Deep-sea species also possess large OBs, suggesting a greater reliance on olfaction in habitats where vision may be compromised. In contrast, the smallest OBs were found in the majority of reef-associated species, including sharks from the families Carcharhinidae and Hemiscyllidae and dasyatid batoids. These results suggest that there is great variability in the degree to which these fishes rely on olfactory cues. The OBs have been widely used as a neuroanatomical proxy for olfactory capability in vertebrates, and we speculate that differences in olfactory capabilities may be the result of

  11. Mathematical Modeling of Space-Time Variations in Acoustic Transmission and Scattering from Schools of Swim Bladder Fish (FY11 Annual Report)

    DTIC Science & Technology

    2011-09-01

    Chile Facultad de Fı́sica Av. Vicuña Mackenna 4860 Santiago, Chile phone: +56 2 354 4800 fax: +56 2 354 4491 email: chris.feuillade@gmail.com...differential equations, and incorporates a verified swim bladder scattering kernel (Ref. 2 ) for an individual fish. All orders of multiple scattering...currently valid OMB control number. 1. REPORT DATE SEP 2011 2 . REPORT TYPE 3. DATES COVERED 00-00-2011 to 00-00-2011 4. TITLE AND SUBTITLE

  12. Investigation on 3D t wake flow structures of swimming bionic fish

    NASA Astrophysics Data System (ADS)

    Shen, G.-X.; Tan, G.-K.; Lai, G.-J.

    2012-10-01

    A bionic experimental platform was designed for the purpose of investigating time accurate three-dimensional flow field, using digital particle image velocimetry (DSPIV). The wake behind the flapping trail of a robotic fish model was studied at high spatial resolution. The study was performed in a water channel. A robot fish model was designed and built. The model was fixed onto a rigid support framework using a cable-supporting method, with twelve stretched wires. The entire tail of the model can perform prescribed motions in two degrees of freedom, mainly in carangiform mode, by driving its afterbody and lunate caudal fin respectively. The DSPIV system was set up to operate in a translational manner, measuring velocity field in a series of parallel slices. Phase locked measurements were repeated for a number of runs, allowing reconstruction of phase average flow field. Vortex structures with phase history of the wake were obtained. The study reveals some new and complex three-dimensional flow structures in the wake of the fish, including "reverse hairpin vortex" and "reverse Karman S-H vortex rings", allowing insight into physics of this complex flow.

  13. Investigation of flow mechanism of a robotic fish swimming by using flow visualization synchronized with hydrodynamic force measurement

    NASA Astrophysics Data System (ADS)

    Tan, Guang-Kun; Shen, Gong-Xin; Huang, Shuo-Qiao; Su, Wen-Han; Ke, Yu

    When swimming in water by flapping its tail, a fish can overcome the drag from uniform flow and propel its body. The involved flow mechanism concerns 3-D and unsteady effects. This paper presents the investigation of the flow mechanism on the basis of a 3-D robotic fish model which has the typical geometry of body and tail with periodic flapping 2-freedom kinematical motion testing in the case of St = 0.78, Re = 6,600 and phase delay mode (φ = - 75°), in which may have a greater or maximum propulsion (without consideration of the optimal efficiency). Using a special technique of dye visualization which can clearly show vortex sheet and vortices in detail and using the inner 3-component force balance and cable supporting system with the phase-lock technique, the 3-D flow structure visualized in the wake of fish and the hydrodynamic force measurement were synchronized and obtained. Under the mentioned flapping parameters, we found the key flow structure and its evolution, a pair of complex 3-D chain-shape vortex (S-H vortex-rings, S1 - H1 and S2 - H2, and their legs L1 and L2) flow structures, which attach the leading edge and the trailing edge, then shed, move downstream and outwards and distribute two antisymmetric staggering arrays along with the wake of the fish model in different phase stages during the flapping period. It is different with in the case of St = 0.25-0.35. Its typical flow structure and evolution are described and the results prove that they are different from the viewpoints based on the investigation of 2-D cases. For precision of the dynamic force measurement, in this paper it was provided with the method and techniques by subtracting the inertial forces and the forces induced by buoyancy and gravity effect in water, etc. from original data measured. The evolution of the synchronized measuring forces directly matching with the flow structure was also described in this paper.

  14. Investigation of flow mechanism of a robotic fish swimming by using flow visualization synchronized with hydrodynamic force measurement

    NASA Astrophysics Data System (ADS)

    Tan, Guang-Kun; Shen, Gong-Xin; Huang, Shuo-Qiao; Su, Wen-Han; Ke, Yu

    2007-11-01

    When swimming in water by flapping its tail, a fish can overcome the drag from uniform flow and propel its body. The involved flow mechanism concerns 3-D and unsteady effects. This paper presents the investigation of the flow mechanism on the basis of a 3-D robotic fish model which has the typical geometry of body and tail with periodic flapping 2-freedom kinematical motion testing in the case of St = 0.78, Re = 6,600 and phase delay mode ( φ = -75°), in which may have a greater or maximum propulsion (without consideration of the optimal efficiency). Using a special technique of dye visualization which can clearly show vortex sheet and vortices in detail and using the inner 3-component force balance and cable supporting system with the phase-lock technique, the 3-D flow structure visualized in the wake of fish and the hydrodynamic force measurement were synchronized and obtained. Under the mentioned flapping parameters, we found the key flow structure and its evolution, a pair of complex 3-D chain-shape vortex (S-H vortex-rings, S1-H1 and S2-H2, and their legs L1 and L2) flow structures, which attach the leading edge and the trailing edge, then shed, move downstream and outwards and distribute two anti-symmetric staggering arrays along with the wake of the fish model in different phase stages during the flapping period. It is different with in the case of St = 0.25-0.35. Its typical flow structure and evolution are described and the results prove that they are different from the viewpoints based on the investigation of 2-D cases. For precision of the dynamic force measurement, in this paper it was provided with the method and techniques by subtracting the inertial forces and the forces induced by buoyancy and gravity effect in water, etc. from original data measured. The evolution of the synchronized measuring forces directly matching with the flow structure was also described in this paper.

  15. Fractional rate of change of swim-bladder volume is reliably related to absolute depth during vertical displacements in teleost fish.

    PubMed

    Taylor, Graham K; Holbrook, Robert Iain; de Perera, Theresa Burt

    2010-09-06

    Fish must orient in three dimensions as they navigate through space, but it is unknown whether they are assisted by a sense of depth. In principle, depth can be estimated directly from hydrostatic pressure, but although teleost fish are exquisitely sensitive to changes in pressure, they appear unable to measure absolute pressure. Teleosts sense changes in pressure via changes in the volume of their gas-filled swim-bladder, but because the amount of gas it contains is varied to regulate buoyancy, this cannot act as a long-term steady reference for inferring absolute pressure. In consequence, it is generally thought that teleosts are unable to sense depth using hydrostatic pressure. Here, we overturn this received wisdom by showing from a theoretical physical perspective that absolute depth could be estimated during fast, steady vertical displacements by combining a measurement of vertical speed with a measurement of the fractional rate of change of swim-bladder volume. This mechanism works even if the amount of gas in the swim-bladder varies, provided that this variation occurs over much longer time scales than changes in volume during displacements. There is therefore no a priori physical justification for assuming that teleost fish cannot sense absolute depth by using hydrostatic pressure cues.

  16. Real-Time Localization of Moving Dipole Sources for Tracking Multiple Free-Swimming Weakly Electric Fish.

    PubMed

    Jun, James Jaeyoon; Longtin, André; Maler, Leonard

    2013-01-01

    In order to survive, animals must quickly and accurately locate prey, predators, and conspecifics using the signals they generate. The signal source location can be estimated using multiple detectors and the inverse relationship between the received signal intensity (RSI) and the distance, but difficulty of the source localization increases if there is an additional dependence on the orientation of a signal source. In such cases, the signal source could be approximated as an ideal dipole for simplification. Based on a theoretical model, the RSI can be directly predicted from a known dipole location; but estimating a dipole location from RSIs has no direct analytical solution. Here, we propose an efficient solution to the dipole localization problem by using a lookup table (LUT) to store RSIs predicted by our theoretically derived dipole model at many possible dipole positions and orientations. For a given set of RSIs measured at multiple detectors, our algorithm found a dipole location having the closest matching normalized RSIs from the LUT, and further refined the location at higher resolution. Studying the natural behavior of weakly electric fish (WEF) requires efficiently computing their location and the temporal pattern of their electric signals over extended periods. Our dipole localization method was successfully applied to track single or multiple freely swimming WEF in shallow water in real-time, as each fish could be closely approximated by an ideal current dipole in two dimensions. Our optimized search algorithm found the animal's positions, orientations, and tail-bending angles quickly and accurately under various conditions, without the need for calibrating individual-specific parameters. Our dipole localization method is directly applicable to studying the role of active sensing during spatial navigation, or social interactions between multiple WEF. Furthermore, our method could be extended to other application areas involving dipole source

  17. Real-Time Localization of Moving Dipole Sources for Tracking Multiple Free-Swimming Weakly Electric Fish

    PubMed Central

    Jun, James Jaeyoon; Longtin, André; Maler, Leonard

    2013-01-01

    In order to survive, animals must quickly and accurately locate prey, predators, and conspecifics using the signals they generate. The signal source location can be estimated using multiple detectors and the inverse relationship between the received signal intensity (RSI) and the distance, but difficulty of the source localization increases if there is an additional dependence on the orientation of a signal source. In such cases, the signal source could be approximated as an ideal dipole for simplification. Based on a theoretical model, the RSI can be directly predicted from a known dipole location; but estimating a dipole location from RSIs has no direct analytical solution. Here, we propose an efficient solution to the dipole localization problem by using a lookup table (LUT) to store RSIs predicted by our theoretically derived dipole model at many possible dipole positions and orientations. For a given set of RSIs measured at multiple detectors, our algorithm found a dipole location having the closest matching normalized RSIs from the LUT, and further refined the location at higher resolution. Studying the natural behavior of weakly electric fish (WEF) requires efficiently computing their location and the temporal pattern of their electric signals over extended periods. Our dipole localization method was successfully applied to track single or multiple freely swimming WEF in shallow water in real-time, as each fish could be closely approximated by an ideal current dipole in two dimensions. Our optimized search algorithm found the animal’s positions, orientations, and tail-bending angles quickly and accurately under various conditions, without the need for calibrating individual-specific parameters. Our dipole localization method is directly applicable to studying the role of active sensing during spatial navigation, or social interactions between multiple WEF. Furthermore, our method could be extended to other application areas involving dipole source

  18. "The fish becomes aware of the water in which it swims": revealing the power of culture in shaping teaching identity

    NASA Astrophysics Data System (ADS)

    Rahmawati, Yuli; Taylor, Peter Charles

    2017-08-01

    "The fish becomes aware of the water in which it swims" is a metaphor that represents Yuli's revelatory journey about the hidden power of culture in her personal identity and professional teaching practice. While engaging in a critical auto/ethnographic inquiry into her lived experience as a science teacher in Indonesian and Australian schools, she came to understand the powerful role of culture in shaping her teaching identity. Yuli realised that she is a product of cultural hybridity resulting from interactions of very different cultures—Javanese, Bimanese, Indonesian and Australian. Traditionally, Javanese and Indonesian cultures do not permit direct criticism of others. This influenced strongly the way she had learned to interact with students and caused her to be very sensitive to others. During this inquiry she learned the value of engaging students in open discourse and overt caring, and came to realise that teachers bringing their own cultures to the classroom can be both a source of power and a problem. In this journey, Yuli came to understand the hegemonic power of culture in her teaching identity, and envisioned how to empower herself as a good teacher educator of pre-service science teachers.

  19. The IL-1 family in fish: swimming through the muddy waters of inflammasome evolution.

    PubMed

    Ogryzko, Nikolay V; Renshaw, Stephen A; Wilson, Heather L

    2014-09-01

    Inflammatory diseases are a significant burden on global healthcare systems, and tackling these diseases is a major focus of modern medicine. Key to many inflammatory diseases is the cytokine, Interleukin-1 (IL-1). Due to its apical role in initiating the inflammatory response, dysregulated IL-1 signalling results in a number of pathologies. Treatment of inflammatory diseases with anti-IL-1 therapies has offered many therapeutic benefits, however current therapies are protein based, with all the accompanying limitations. The non-conventional pathways involved in IL-1 signalling provide a number of potential therapeutic targets for clinical intervention and this has led to the exploitation of a number of model organisms for the study of IL-1 biology. Murine models have long been used to study IL-1 processing and release, but do not allow direct visualisation in vivo. Recently, fish models have emerged as genetically tractable and optically transparent inflammatory disease models. These models have raised questions on the evolutionary origins of the IL-1 family and the conservation in its processing and activation. Here we review the current understanding of IL-1 evolution in fish and discuss the study of IL-1 processing in these models.

  20. Inorganic mercury accumulation in brain following waterborne exposure elicits a deficit on the number of brain cells and impairs swimming behavior in fish (white seabream-Diplodus sargus).

    PubMed

    Pereira, Patrícia; Puga, Sónia; Cardoso, Vera; Pinto-Ribeiro, Filipa; Raimundo, Joana; Barata, Marisa; Pousão-Ferreira, Pedro; Pacheco, Mário; Almeida, Armando

    2016-01-01

    The current study contributes to fill the knowledge gap on the neurotoxicity of inorganic mercury (iHg) in fish through the implementation of a combined evaluation of brain morphometric alterations (volume and total number of neurons plus glial cells in specific regions of the brain) and swimming behavior (endpoints related with the motor activity and mood/anxiety-like status). White seabream (Diplodus sargus) was exposed to realistic levels of iHg in water (2μgL(-1)) during 7 (E7) and 14 days (E14). After that, fish were allowed to recover for 28 days (PE28) in order to evaluate brain regeneration and reversibility of behavioral syndromes. A significant reduction in the number of cells in hypothalamus, optic tectum and cerebellum was found at E7, accompanied by relevant changes on swimming behavior. Moreover, the decrease in the number of neurons and glia in the molecular layer of the cerebellum was followed by a contraction of its volume. This is the first time that a deficit on the number of cells is reported in fish brain after iHg exposure. Interestingly, a recovery of hypothalamus and cerebellum occurred at E14, as evidenced by the identical number of cells found in exposed and control fish, and volume of cerebellum, which might be associated with an adaptive phenomenon. After 28 days post-exposure, the optic tectum continued to show a decrease in the number of cells, pointing out a higher vulnerability of this region. These morphometric alterations coincided with numerous changes on swimming behavior, related both with fish motor function and mood/anxiety-like status. Overall, current data pointed out the iHg potential to induce brain morphometric alterations, emphasizing a long-lasting neurobehavioral hazard. Copyright © 2015 Elsevier B.V. All rights reserved.

  1. Developmental intervals during the larval and juvenile stages of the Antarctic myctophid fish Electrona antarctica in relation to changes in feeding and swimming functions

    NASA Astrophysics Data System (ADS)

    Moteki, Masato; Tsujimura, Eri; Hulley, Percy-Alexander

    2017-06-01

    The Antarctic myctophid fish species Electrona antarctica is believed to play a key role in the Southern Ocean food web, but there have been few studies on its early life history. This study examined the developmental changes in the external morphology and osteology of E. antarctica from the early larva to juvenile stages through the transformation phase and inferred changes in its behaviour and feeding mode. Once the larvae reached 12-13 mm body length (BL), they adopted a primordial suction feeding mode along with the acquisition of early swimming capabilities. Thereafter, both swimming and feeding functions were enhanced through fin development and ossification and acquisition of elements of the jaw and suspensorium. These processes indicate that larvae transition from the planktonic to nektonic phase upon reaching 12-13 mm BL when they enhance their both swimming and feeding abilities with growth. Transformation occurred when larvae reached 19-21 mm BL with changes such as discontinuous increases in eye diameter and upper jaw length and the appearance of photophores and dense body pigmentation. Osteological development of swimming- and feeding-related structures were mostly complete after transformation. Rapid changes in external morphology and osteology during the transformation stage are most likely related to ontogenetic vertical migration into deep waters.

  2. Maximum swimming speeds of sailfish and three other large marine predatory fish species based on muscle contraction time and stride length: a myth revisited.

    PubMed

    Svendsen, Morten B S; Domenici, Paolo; Marras, Stefano; Krause, Jens; Boswell, Kevin M; Rodriguez-Pinto, Ivan; Wilson, Alexander D M; Kurvers, Ralf H J M; Viblanc, Paul E; Finger, Jean S; Steffensen, John F

    2016-10-15

    Billfishes are considered to be among the fastest swimmers in the oceans. Previous studies have estimated maximum speed of sailfish and black marlin at around 35 m s(-1) but theoretical work on cavitation predicts that such extreme speed is unlikely. Here we investigated maximum speed of sailfish, and three other large marine pelagic predatory fish species, by measuring the twitch contraction time of anaerobic swimming muscle. The highest estimated maximum swimming speeds were found in sailfish (8.3±1.4 m s(-1)), followed by barracuda (6.2±1.0 m s(-1)), little tunny (5.6±0.2 m s(-1)) and dorado (4.0±0.9 m s(-1)); although size-corrected performance was highest in little tunny and lowest in sailfish. Contrary to previously reported estimates, our results suggest that sailfish are incapable of exceeding swimming speeds of 10-15 m s(-1), which corresponds to the speed at which cavitation is predicted to occur, with destructive consequences for fin tissues. © 2016. Published by The Company of Biologists Ltd.

  3. Maximum swimming speeds of sailfish and three other large marine predatory fish species based on muscle contraction time and stride length: a myth revisited

    PubMed Central

    Svendsen, Morten B. S.; Domenici, Paolo; Marras, Stefano; Krause, Jens; Boswell, Kevin M.; Rodriguez-Pinto, Ivan; Wilson, Alexander D. M.; Kurvers, Ralf H. J. M.; Viblanc, Paul E.; Finger, Jean S.; Steffensen, John F.

    2016-01-01

    ABSTRACT Billfishes are considered to be among the fastest swimmers in the oceans. Previous studies have estimated maximum speed of sailfish and black marlin at around 35 m s−1 but theoretical work on cavitation predicts that such extreme speed is unlikely. Here we investigated maximum speed of sailfish, and three other large marine pelagic predatory fish species, by measuring the twitch contraction time of anaerobic swimming muscle. The highest estimated maximum swimming speeds were found in sailfish (8.3±1.4 m s−1), followed by barracuda (6.2±1.0 m s−1), little tunny (5.6±0.2 m s−1) and dorado (4.0±0.9 m s−1); although size-corrected performance was highest in little tunny and lowest in sailfish. Contrary to previously reported estimates, our results suggest that sailfish are incapable of exceeding swimming speeds of 10-15 m s−1, which corresponds to the speed at which cavitation is predicted to occur, with destructive consequences for fin tissues. PMID:27543056

  4. Bioinspired swimming simulations

    NASA Astrophysics Data System (ADS)

    Bergmann, Michel; Iollo, Angelo

    2016-10-01

    We present a method to simulate the flow past bioinspired swimmers starting from pictures of an actual fish. The overall approach requires i) a skeleton graph generation to get a level-set function from pictures; ii) optimal transportation to obtain the velocity on the body surface; iii) flow simulations realized with a Cartesian method based on penalization. This technique can be used to automate modeling swimming motion from data collected by biologists. We illustrate this paradigm by simulating the swimming of a mackerel fish.

  5. Swimming ability and behaviour of post-larvae of a temperate marine fish re-entrained in the pelagic environment.

    PubMed

    Hindell, Jeremy S; Jenkins, Gregory P; Moran, Sean M; Keough, Michael J

    2003-03-01

    The degree to which behaviour, vertical movement and horizontal transport, in relation to local hydrodynamics, may facilitate secondary dispersal in the water column was studied in post-larval Sillaginodes punctata in Port Phillip Bay, Australia. S. punctata were captured in shallow seagrass beds and released at the surface in three depth zones (1.5, 3 and 7 m) off-shore at each of two sites to mimic the re-entrainment of fish. The behaviour, depth and position of S. punctata were recorded through time. The direction and speed of local currents were described using an S4 current meter and the movement of drogues. Regardless of site, fish immediately oriented toward the bottom, and into the current after release. In shallow water (1.5 m), 86% of fish swam to the bottom within 2 min of release. At one site, the net horizontal displacement of fish was largely unrelated to the speed and direction of local currents; at a second site, fish could not maintain their position against the current, and the net horizontal displacement was related to the speed and direction of currents. In the intermediate depth zone, wide variability in depths of individual fish through time led to an average depth reached by fish that was between the shallow and deep zones. Based on daily increments in the otoliths, however, this variability was not related significantly to the time since entry of fish into Port Phillip Bay. In the deepest depth zone, 81% of fish remained within 1 m of the surface and their horizontal displacement was significantly related to the direction and speed of currents. Secondary dispersal of post-larval fish in the water column may be facilitated by the behaviour and vertical movements of fish, but only if fish reach deeper water, where their displacement (direction and distance) closely resembles local hydrodynamic regimes. In shallow water, fish behaviour and vertical migration actually reduce the potential for secondary dispersal.

  6. Boundary layer control by a fish: Unsteady laminar boundary layers of rainbow trout swimming in turbulent flows

    PubMed Central

    Saarenrinne, Pentti

    2016-01-01

    ABSTRACT The boundary layers of rainbow trout, Oncorhynchus mykiss [0.231±0.016 m total body length (L) (mean±s.d.); N=6], swimming at 1.6±0.09 L s−1 (N=6) in an experimental flow channel (Reynolds number, Re=4×105) with medium turbulence (5.6% intensity) were examined using the particle image velocimetry technique. The tangential flow velocity distributions in the pectoral and pelvic surface regions (arc length from the rostrum, lx=71±8 mm, N=3, and lx=110±13 mm, N=4, respectively) were approximated by a laminar boundary layer model, the Falkner−Skan equation. The flow regime over the pectoral and pelvic surfaces was regarded as a laminar flow, which could create less skin-friction drag than would be the case with turbulent flow. Flow separation was postponed until vortex shedding occurred over the posterior surface (lx=163±22 mm, N=3). The ratio of the body-wave velocity to the swimming speed was in the order of 1.2. This was consistent with the condition of the boundary layer laminarization that had been confirmed earlier using a mechanical model. These findings suggest an energy-efficient swimming strategy for rainbow trout in a turbulent environment. PMID:27815242

  7. Effects of nitrite exposure on functional haemoglobin levels, bimodal respiration, and swimming performance in the facultative air-breathing fish Pangasianodon hypophthalmus.

    PubMed

    Lefevre, Sjannie; Jensen, Frank B; Huong, Do T T; Wang, Tobias; Phuong, Nguyen T; Bayley, Mark

    2011-07-01

    In this study we investigated nitrite (NO₂⁻) effects in striped catfish, a facultative air-breather. Fish were exposed to 0, 0.4, and 0.9 mM nitrite for 0, 1, 2, 4, and 7 days, and levels of functional haemoglobin, methaemoglobin (metHb) and nitrosyl haemoglobin (HbNO) were assessed using spectral deconvolution. Plasma concentrations of nitrite, nitrate, chloride, potassium, and sodium were also measured. Partitioning of oxygen consumption was determined to reveal whether elevated metHb (causing functional hypoxia) induced air-breathing. The effects of nitrite on maximum oxygen uptake (MO(2max)) and critical swimming speed (U(crit)) were also assessed. Striped catfish was highly tolerant to nitrite exposure, as reflected by a 96 h LC₅₀ of 1.65 mM and a moderate nitrite uptake into the blood. Plasma levels of nitrite reached a maximum after 1 day of exposure, and then decreased, never exceeding ambient levels. MetHb, HbNO and nitrate (a nitrite detoxification product) also peaked after 1 day and then decreased. Only high levels of nitrite and metHb caused reductions in MO(2max) and U(crit). The response of striped catfish contrasts with that seen in most other fish species and discloses efficient mechanisms of combating nitrite threats. Furthermore, even though striped catfish is an efficient air-breather, this species has the ability to sustain aerobic scope and swimming performance without air-breathing, even when faced with nitrite-induced reductions in blood oxygen carrying capacity. Our study is the first to confirm that high levels of nitrite and metHb reduce MO(2max) and thereby aerobic scope, while more moderate elevations fail to do so. Further studies are needed to elucidate the mechanisms underlying the low nitrite accumulation in striped catfish.

  8. Automatic realistic real time stimulation/recording in weakly electric fish: long time behavior characterization in freely swimming fish and stimuli discrimination.

    PubMed

    Forlim, Caroline G; Pinto, Reynaldo D

    2014-01-01

    Weakly electric fish are unique model systems in neuroethology, that allow experimentalists to non-invasively, access, central nervous system generated spatio-temporal electric patterns of pulses with roles in at least 2 complex and incompletely understood abilities: electrocommunication and electrolocation. Pulse-type electric fish alter their inter pulse intervals (IPIs) according to different behavioral contexts as aggression, hiding and mating. Nevertheless, only a few behavioral studies comparing the influence of different stimuli IPIs in the fish electric response have been conducted. We developed an apparatus that allows real time automatic realistic stimulation and simultaneous recording of electric pulses in freely moving Gymnotus carapo for several days. We detected and recorded pulse timestamps independently of the fish's position for days. A stimulus fish was mimicked by a dipole electrode that reproduced the voltage time series of real conspecific according to previously recorded timestamp sequences. We characterized fish behavior and the eletrocommunication in 2 conditions: stimulated by IPIs pre-recorded from other fish and random IPI ones. All stimuli pulses had the exact Gymontus carapo waveform. All fish presented a surprisingly long transient exploratory behavior (more than 8 h) when exposed to a new environment in the absence of electrical stimuli. Further, we also show that fish are able to discriminate between real and random stimuli distributions by changing several characteristics of their IPI distribution.

  9. Optimality Principles of Undulatory Swimming

    NASA Astrophysics Data System (ADS)

    Nangia, Nishant; Bale, Rahul; Patankar, Neelesh

    2015-11-01

    A number of dimensionless quantities derived from a fish's kinematic and morphological parameters have been used to describe the hydrodynamics of swimming. In particular, body/caudal fin swimmers have been found to swim within a relatively narrow range of these quantities in nature, e.g., Strouhal number or the optimal specific wavelength. It has been hypothesized or shown that these constraints arise due to maximization of swimming speed, efficiency, or cost of transport in certain domains of this large dimensionless parameter space. Using fully resolved simulations of undulatory patterns, we investigate the existence of various optimality principles in fish swimming. Using scaling arguments, we relate various dimensionless parameters to each other. Based on these findings, we make design recommendations on how kinematic parameters for a swimming robot or vehicle should be chosen. This work is supported by NSF Grants CBET-0828749, CMMI-0941674, CBET-1066575 and the National Science Foundation Graduate Research Fellowship under Grant No. DGE-1324585.

  10. Female "Big Fish" Swimming against the Tide: The "Big-Fish-Little-Pond Effect" and Gender-Ratio in Special Gifted Classes

    ERIC Educational Resources Information Center

    Preckel, Franzis; Zeidner, Moshe; Goetz, Thomas; Schleyer, Esther Jane

    2008-01-01

    This study takes a second look at the "big-fish-little-pond effect" (BFLPE) on a national sample of 769 gifted Israeli students (32% female) previously investigated by Zeidner and Schleyer (Zeidner, M., & Schleyer, E. J., (1999a). "The big-fish-little-pond effect for academic self-concept, test anxiety, and school grades in…

  11. Automatic Realistic Real Time Stimulation/Recording in Weakly Electric Fish: Long Time Behavior Characterization in Freely Swimming Fish and Stimuli Discrimination

    PubMed Central

    Forlim, Caroline G.; Pinto, Reynaldo D.

    2014-01-01

    Weakly electric fish are unique model systems in neuroethology, that allow experimentalists to non-invasively, access, central nervous system generated spatio-temporal electric patterns of pulses with roles in at least 2 complex and incompletely understood abilities: electrocommunication and electrolocation. Pulse-type electric fish alter their inter pulse intervals (IPIs) according to different behavioral contexts as aggression, hiding and mating. Nevertheless, only a few behavioral studies comparing the influence of different stimuli IPIs in the fish electric response have been conducted. We developed an apparatus that allows real time automatic realistic stimulation and simultaneous recording of electric pulses in freely moving Gymnotus carapo for several days. We detected and recorded pulse timestamps independently of the fish’s position for days. A stimulus fish was mimicked by a dipole electrode that reproduced the voltage time series of real conspecific according to previously recorded timestamp sequences. We characterized fish behavior and the eletrocommunication in 2 conditions: stimulated by IPIs pre-recorded from other fish and random IPI ones. All stimuli pulses had the exact Gymontus carapo waveform. All fish presented a surprisingly long transient exploratory behavior (more than 8 h) when exposed to a new environment in the absence of electrical stimuli. Further, we also show that fish are able to discriminate between real and random stimuli distributions by changing several characteristics of their IPI distribution. PMID:24400122

  12. Female "Big Fish" Swimming against the Tide: The "Big-Fish-Little-Pond Effect" and Gender-Ratio in Special Gifted Classes

    ERIC Educational Resources Information Center

    Preckel, Franzis; Zeidner, Moshe; Goetz, Thomas; Schleyer, Esther Jane

    2008-01-01

    This study takes a second look at the "big-fish-little-pond effect" (BFLPE) on a national sample of 769 gifted Israeli students (32% female) previously investigated by Zeidner and Schleyer (Zeidner, M., & Schleyer, E. J., (1999a). "The big-fish-little-pond effect for academic self-concept, test anxiety, and school grades in…

  13. An implantable two axis micromanipulator made with a 3D printer for recording neural activity in free-swimming fish.

    PubMed

    Rogers, Loranzie S; Van Wert, Jacey C; Mensinger, Allen F

    2017-08-15

    Chronically implanted electrodes allow monitoring neural activity from free moving animals. While a wide variety of implanted headstages, microdrives and electrodes exist for terrestrial animals, few have been developed for use with aquatic animals. A two axis micromanipulator was fabricated with a Formlabs 3D printer for implanting electrodes into free-swimming oyster toadfish (Opsanus tau). The five piece manipulator consisted of a base, body, electrode holder, manual screw drive and locking nut. The manipulator measured approximately 25×20×30mm (l×w×h) and weighed 5.28g after hand assembly. Microwire electrodes were inserted successfully with the manipulator to record high fidelity signals from the anterior lateral line nerve of the toadfish. The micromanipulator allowed the chronically implanted electrodes to be repositioned numerous times to record from multiple sites and extended successful recording time in the toadfish by several days. Three dimensional printing allowed an inexpensive (<$US 5 material), two axis micromanipulator to be printed relatively rapidly (<2h) to successfully record from multiple sites in the anterior lateral line nerve of free-swimming toadfish. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Automated pulse discrimination of two freely-swimming weakly electric fish and analysis of their electrical behavior during dominance contest.

    PubMed

    Guariento, Rafael T; Mosqueiro, Thiago S; Matias, Paulo; Cesarino, Vinicius B; Almeida, Lirio O B; Slaets, Jan F W; Maia, Leonardo P; Pinto, Reynaldo D

    2017-02-07

    Electric fishes modulate their electric organ discharges with a remarkable variability. Some patterns can be easily identified, such as pulse rate changes, offs and chirps, which are often associated with important behavioral contexts, including aggression, hiding and mating. However, these behaviors are only observed when at least two fish are freely interacting. Although their electrical pulses can be easily recorded by non-invasive techniques, discriminating the emitter of each pulse is challenging when physically similar fish are allowed to freely move and interact. Here we optimized a custom-made software recently designed to identify the emitter of pulses by using automated chirp detection, adaptive threshold for pulse detection and slightly changing how the recorded signals are integrated. With these optimizations, we performed a quantitative analysis of the statistical changes throughout the dominance contest with respect to Inter Pulse Intervals, Chirps and Offs dyads of freely moving Gymnotus carapo. In all dyads, chirps were signatures of subsequent submission, even when they occurred early in the contest. Although offs were observed in both dominant and submissive fish, they were substantially more frequent in submissive individuals, in agreement with the idea from previous studies that offs are electric cues of submission. In general, after the dominance is established the submissive fish significantly changes its average pulse rate, while the pulse rate of the dominant remained unchanged. Additionally, no chirps or offs were observed when two fish were manually kept in direct physical contact, suggesting that these electric behaviors are not automatic responses to physical contact.

  15. Seahorses under a changing ocean: the impact of warming and acidification on the behaviour and physiology of a poor-swimming bony-armoured fish.

    PubMed

    Faleiro, Filipa; Baptista, Miguel; Santos, Catarina; Aurélio, Maria L; Pimentel, Marta; Pegado, Maria Rita; Paula, José Ricardo; Calado, Ricardo; Repolho, Tiago; Rosa, Rui

    2015-01-01

    Seahorses are currently facing great challenges in the wild, including habitat degradation and overexploitation, and how they will endure additional stress from rapid climate change has yet to be determined. Unlike most fishes, the poor swimming skills of seahorses, along with the ecological and biological constraints of their unique lifestyle, place great weight on their physiological ability to cope with climate changes. In the present study, we evaluate the effects of ocean warming (+4°C) and acidification (ΔpH = -0.5 units) on the physiological and behavioural ecology of adult temperate seahorses, Hippocampus guttulatus. Adult seahorses were found to be relatively well prepared to face future changes in ocean temperature, but not the combined effect of warming and acidification. Seahorse metabolism increased normally with warming, and behavioural and feeding responses were not significantly affected. However, during hypercapnia the seahorses exhibited signs of lethargy (i.e. reduced activity levels) combined with a reduction of feeding and ventilation rates. Nonetheless, metabolic rates were not significantly affected. Future ocean changes, particularly ocean acidification, may further threaten seahorse conservation, turning these charismatic fishes into important flagship species for global climate change issues.

  16. Fish and chips: implementation of a neural network model into computer chips to maximize swimming efficiency in autonomous underwater vehicles.

    PubMed

    Blake, R W; Ng, H; Chan, K H S; Li, J

    2008-09-01

    Recent developments in the design and propulsion of biomimetic autonomous underwater vehicles (AUVs) have focused on boxfish as models (e.g. Deng and Avadhanula 2005 Biomimetic micro underwater vehicle with oscillating fin propulsion: system design and force measurement Proc. 2005 IEEE Int. Conf. Robot. Auto. (Barcelona, Spain) pp 3312-7). Whilst such vehicles have many potential advantages in operating in complex environments (e.g. high manoeuvrability and stability), limited battery life and payload capacity are likely functional disadvantages. Boxfish employ undulatory median and paired fins during routine swimming which are characterized by high hydromechanical Froude efficiencies (approximately 0.9) at low forward speeds. Current boxfish-inspired vehicles are propelled by a low aspect ratio, 'plate-like' caudal fin (ostraciiform tail) which can be shown to operate at a relatively low maximum Froude efficiency (approximately 0.5) and is mainly employed as a rudder for steering and in rapid swimming bouts (e.g. escape responses). Given this and the fact that bioinspired engineering designs are not obligated to wholly duplicate a biological model, computer chips were developed using a multilayer perception neural network model of undulatory fin propulsion in the knifefish Xenomystus nigri that would potentially allow an AUV to achieve high optimum values of propulsive efficiency at any given forward velocity, giving a minimum energy drain on the battery. We envisage that externally monitored information on flow velocity (sensory system) would be conveyed to the chips residing in the vehicle's control unit, which in turn would signal the locomotor unit to adopt kinematics (e.g. fin frequency, amplitude) associated with optimal propulsion efficiency. Power savings could protract vehicle operational life and/or provide more power to other functions (e.g. communications).

  17. Emulating the Fast-Start Swimming Performance of the Chain Pickerel (Esox niger) Using a Mechanical Fish Design

    DTIC Science & Technology

    2006-09-01

    fuels the mechanical fish is introduced by deflecting the stiff beam. The greater the deflection, the more energy that is imparted to the system. For...peak velocity continue to fuel the second vortex induced propulsive jet for a short time. Further images, not displayed here, show the steady

  18. Importance of mechanics and kinematics in determining the stiffness contribution of the vertebral column during body-caudal-fin swimming in fishes.

    PubMed

    Nowroozi, Bryan N; Brainerd, Elizabeth L

    2014-02-01

    Whole-body stiffness in fishes has important consequences for swimming mode, speed and efficiency, but the contribution of vertebral column stiffness to whole-body stiffness is unclear. In our opinion, this lack of clarity is due in part to the lack of studies that have measured both in vitro mechanical properties of the vertebral column as well as in vivo vertebral kinematics in the same species. Some lack of clarity may also come from real variation in the mechanical role of the vertebral column across species. Previous studies, based on either mechanics or kinematics alone, suggest species-specific variation in vertebral column locomotor function that ranges from highly stiff regimes that contribute greatly to whole-body stiffness, and potentially act as a spring, to highly compliant regimes that only prohibit excessive flexion of the intervertebral joints. We review data collected in combined investigations of both mechanics and kinematics of three species, Myxine glutinosa, Acipenser transmontanus, and Morone saxatilis, to illustrate how mechanical testing within the context of the in vivo kinematics more clearly distinguishes the role of the vertebral column in each species. In addition, we identify species for which kinematic data are available, but mechanical data are lacking. We encourage further investigation of these species to fill these mechanical data gaps. Finally, we hope these future combined analyses will identify certain morphological, mechanical, or kinematic parameters that might be associated with certain vertebral column functional regimes with respect to body stiffness.

  19. Bobcat Walking and Swimming

    NASA Image and Video Library

    2014-03-06

    CAPE CANAVERAL, Fla. – A bobcat leaves a trail as it swims across an algae-covered canal near the NASA News Center at Kennedy Space Center in Florida. The center shares a boundary with the Merritt Island National Wildlife Refuge. The refuge encompasses 140,000 acres that are a habitat for more than 330 species of birds, 31 mammals, 117 fishes, and 65 amphibians and reptiles. Photo credit: NASA/Daniel Casper

  20. Fish gotta swim, Birds gotta fly, I gotta do Feynmann Graphs 'til I die: A continuum Theory of Flocking

    NASA Astrophysics Data System (ADS)

    Toner, John; Tu, Yu-Hai

    2002-05-01

    We have developed a new continuum dynamical model for the collective motion of large "flocks" of biological organisms (e.g., flocks of birds, schools of fish, herds of wildebeest, hordes of bacteria, slime molds, etc.) . This model does for flocks what the Navier-Stokes equation does for fluids. The model predicts that, unlike simple fluids, flocks show huge fluctuation effects in spatial dimensions d < 4 that radically change their behavior. In d=2, it is only these effects that make it possible for the flock to move coherently at all. This explains why a million wildebeest can march together across the Serengeti plain, despite the fact that a million physicists gathered on the same plane could NOT all POINT in the same direction. Detailed quantitative predictions of this theory agree beautifully with computer simulations of flock motion.

  1. Factors affecting swimming performance of fasted rainbow trout with implications of exhaustive exercise on overwinter mortality

    USGS Publications Warehouse

    Simpkins, D.G.; Hubert, W.A.; Del Rio, C.M.; Rule, D.C.

    2004-01-01

    We evaluated the effects of body size, water temperature, and sustained swimming activity on swimming performance and the effects of exhaustive exercise on mortality of fasted juvenile rainbow trout. Fasting caused swimming performance to decline more rapidly for small fish than large fish, and warmer water temperatures and sustained swimming activity further decreased swimming performance. Exhaustive exercise increased mortality among fasted fish. Our observations suggest that juvenile rainbow trout with little or no food intake during winter can swim for long periods of time with little effect on mortality, but swimming to exhaustion can enhance mortality, especially among the smallest juveniles.

  2. Swim pressure of active matter

    NASA Astrophysics Data System (ADS)

    Takatori, Sho; Yan, Wen; Brady, John; Caltech Team

    2014-11-01

    Through their self-motion, all active matter systems generate a unique ``swim pressure'' that is entirely athermal in origin. This new source for the active stress exists at all scales in both living and nonliving active systems, and also applies to larger organisms where inertia is important (i.e., the Stokes number is not small). Here we explain the origin of the swim stress and develop a simple thermodynamic model to study the self-assembly and phase separation in active soft matter. Our new swim stress perspective can help analyze and exploit a wide class of active soft matter, from swimming bacteria and catalytic nanobots, schools of fish and birds, and molecular motors that activate the cellular cytoskeleton.

  3. The Swim Pressure of Active Matter

    NASA Astrophysics Data System (ADS)

    Brady, John; Takatori, Sho; Yan, Wen

    2015-03-01

    Through their self-motion, active matter systems generate a unique ``swim pressure'' that is entirely athermal in origin. This new source for the active stress exists at all scales in both living and nonliving active systems, and also applies to larger organisms where inertia is important. Here we explain the origin of the swim stress and develop a simple thermodynamic model to study the self-assembly and phase separation in active soft matter. Our new swim stress perspective may help analyze and exploit a wide class of active soft matter, from swimming bacteria and catalytic nanobots, schools of fish and birds, and molecular motors that activate the cellular cytoskeleton.

  4. Swimming Emergencies

    PubMed Central

    Beerman, Stephen B.

    1988-01-01

    Persons who have undergone swimming emergencies are seen in emergency departments everywhere. They are frequently young healthy citizens. In some instances they will receive better care in large specialized referral hospitals. Other problems can be managed well at local facilities. This article attempts to equip all family physicians with some knowledge and management guidelines for dealing with swimming emergencies, submersion injuries including near-drowning, accidental hypothermia, and triathalon hypothermia. The unique problems of hot tub near-drowning, infant water intoxication, and spinal injuries caused by diving are presented. PMID:21253260

  5. Swimming Performance of Adult Asian Carp: Field Assessment Using a Mobile Swim Tunnel

    DTIC Science & Technology

    2016-08-01

    chute with the river (Varble et al. 2007). The Silver Carp contained in the chute were abundant, large, and sexually mature. Methods. The swim...robustness were < 12% (Table 4). Swimming performance is influenced by a complex suite of factors. These may be intrinsic, such as fish size, reproductive ...impacts on swimming performance were obvious. Gender and reproductive condition were not assessed, but size was relatively uniform. Future studies should

  6. Swimming Pools.

    ERIC Educational Resources Information Center

    Ministry of Housing and Local Government, London (England).

    Technical and engineering data are set forth on the design and construction of swimming pools. Consideration is given to site selection, pool construction, the comparative merits of combining open air and enclosed pools, and alternative uses of the pool. Guidelines are presented regarding--(1) pool size and use, (2) locker and changing rooms, (3)…

  7. Swimming Pools.

    ERIC Educational Resources Information Center

    Ministry of Housing and Local Government, London (England).

    Technical and engineering data are set forth on the design and construction of swimming pools. Consideration is given to site selection, pool construction, the comparative merits of combining open air and enclosed pools, and alternative uses of the pool. Guidelines are presented regarding--(1) pool size and use, (2) locker and changing rooms, (3)…

  8. Swimming capability and swimming behavior of juvenile acipenser schrenckii.

    PubMed

    Cai, Lu; Taupier, Rachel; Johnson, David; Tu, Zhiying; Liu, Guoyong; Huang, Yingping

    2013-03-01

    Acipenser schrenckii, the Amur Sturgeon, was a commercially valuable fish species inhabiting the Amur (Heilongjiang) River but populations have rapidly declined in recent years. Dams impede A. schrenckii spawning migration and wild populations were critically endangered. Building fishways helped maintain fish populations but data on swimming performance and behavior was crucial for fishway design. To obtain such data on A. schrenckii, a laboratory study of juvenile A. schrenckii (n = 18, body mass = 32.7 ± 1.2 g, body length = 18.8 ± 0.3 cm) was conducted using a stepped velocity test carried out in a fish respirometer equipped with a high-speed video camera at 20°C. Results indicate: (1) The counter-current swimming capability of A. schrenckii was low with critical swimming speed of 1.96 ± 0.10 BL/sec. (2) When a linear function was fitted to the data, oxygen consumption, as a function of swimming speed, was determined to be MO2  = 337.29 + 128.10U (R(2)  = 0.971, P < 0.001) and the power value (1.0) of U indicated high swimming efficiency. (3) Excess post-exercise oxygen cost was 48.44 mgO2 /kg and indicated excellent fatigue recovery. (4) Cost of transport decreased slowly with increased swimming speed. (5) Increased swimming speed led to increases in the tail beat frequency and stride length. This investigation contributed to the basic science of fish swimming behavior and provided data required for the design of fishways. Innovative methods have allowed cultivation of the species in the Yangtze River and, if effective fishways could be incorporated into the design of future hydropower projects on the Amur River, it would contribute to conservation of wild populations of A. schrenckii. The information provided here contributes to the international effort to save this critically endangered species. J. Exp. Zool. 319A:149-155, 2013. © 2013 Wiley Periodicals, Inc. Copyright © 2013 Wiley Periodicals, Inc.

  9. Swimming Lessons

    ERIC Educational Resources Information Center

    Goldman, Arthur

    2006-01-01

    In this article, the author talks about his experience as an 11-year-old swimmer and shares the lessons he learned as a member of the swim team. In his experience as one of the slowest team members, he discovered that slow and steady does not win the race, and when the focus is only on achievement, one loses the value of failure. As an adult, he…

  10. Swimming Lessons

    ERIC Educational Resources Information Center

    Goldman, Arthur

    2006-01-01

    In this article, the author talks about his experience as an 11-year-old swimmer and shares the lessons he learned as a member of the swim team. In his experience as one of the slowest team members, he discovered that slow and steady does not win the race, and when the focus is only on achievement, one loses the value of failure. As an adult, he…

  11. Critical swimming speeds of wild bull trout

    USGS Publications Warehouse

    Mesa, M.G.; Weiland, L.K.; Zydlewski, G.B.

    2004-01-01

    We estimated the critical swimming speeds (Ucrit) of wild bull trout at 6??, 11??, and 15??C in laboratory experiments. At 11??C, 5 fish ranging from 11 to 19 cm in length had a mean Ucrit of 48.24 cm/s or 3.22 body lengths per second (BL/s). Also at 11??C , 6 fish from 32 to 42 cm had a mean Ucrit of 73.99 cm/s or 2.05 BL/s. At 15??C, 5 fish from 14 to 23 cm had a mean Ucrit of 54.66 cm/s or 2.88 BL/s. No fish successfully swam at 6??C. Swim speed was significantly influenced by fish length. Many bull trout performed poorly in our enclosed respirometers: of 71 Ucrit tests we attempted, only the 16 described above were successful. Bull trout that refused to swim held station within tunnels by using their pectoral fins as depressors, or they rested and later became impinged against a downstream screen. Several common techniques did not stimulate consistent swimming activity in these fish. Our estimates of U crit for bull trout provide an understanding of their performance capacity and will be useful in modeling efforts aimed at improving fish passage structures. We recommend that fishway or culvert designers concerned with bull trout passage maintain velocities within their structures at or below our estimates of Ucrit, thus taking a conservative approach to ensuring that these fish can ascend migratory obstacles safely.

  12. Intraspecific variation in aerobic and anaerobic locomotion: gilthead sea bream (Sparus aurata) and Trinidadian guppy (Poecilia reticulata) do not exhibit a trade-off between maximum sustained swimming speed and minimum cost of transport

    PubMed Central

    Svendsen, Jon C.; Tirsgaard, Bjørn; Cordero, Gerardo A.; Steffensen, John F.

    2015-01-01

    Intraspecific variation and trade-off in aerobic and anaerobic traits remain poorly understood in aquatic locomotion. Using gilthead sea bream (Sparus aurata) and Trinidadian guppy (Poecilia reticulata), both axial swimmers, this study tested four hypotheses: (1) gait transition from steady to unsteady (i.e., burst-assisted) swimming is associated with anaerobic metabolism evidenced as excess post exercise oxygen consumption (EPOC); (2) variation in swimming performance (critical swimming speed; Ucrit) correlates with metabolic scope (MS) or anaerobic capacity (i.e., maximum EPOC); (3) there is a trade-off between maximum sustained swimming speed (Usus) and minimum cost of transport (COTmin); and (4) variation in Usus correlates positively with optimum swimming speed (Uopt; i.e., the speed that minimizes energy expenditure per unit of distance traveled). Data collection involved swimming respirometry and video analysis. Results showed that anaerobic swimming costs (i.e., EPOC) increase linearly with the number of bursts in S. aurata, with each burst corresponding to 0.53 mg O2 kg−1. Data are consistent with a previous study on striped surfperch (Embiotoca lateralis), a labriform swimmer, suggesting that the metabolic cost of burst swimming is similar across various types of locomotion. There was no correlation between Ucrit and MS or anaerobic capacity in S. aurata indicating that other factors, including morphological or biomechanical traits, influenced Ucrit. We found no evidence of a trade-off between Usus and COTmin. In fact, data revealed significant negative correlations between Usus and COTmin, suggesting that individuals with high Usus also exhibit low COTmin. Finally, there were positive correlations between Usus and Uopt. Our study demonstrates the energetic importance of anaerobic metabolism during unsteady swimming, and provides intraspecific evidence that superior maximum sustained swimming speed is associated with superior swimming economy and

  13. Intraspecific variation in aerobic and anaerobic locomotion: gilthead sea bream (Sparus aurata) and Trinidadian guppy (Poecilia reticulata) do not exhibit a trade-off between maximum sustained swimming speed and minimum cost of transport.

    PubMed

    Svendsen, Jon C; Tirsgaard, Bjørn; Cordero, Gerardo A; Steffensen, John F

    2015-01-01

    Intraspecific variation and trade-off in aerobic and anaerobic traits remain poorly understood in aquatic locomotion. Using gilthead sea bream (Sparus aurata) and Trinidadian guppy (Poecilia reticulata), both axial swimmers, this study tested four hypotheses: (1) gait transition from steady to unsteady (i.e., burst-assisted) swimming is associated with anaerobic metabolism evidenced as excess post exercise oxygen consumption (EPOC); (2) variation in swimming performance (critical swimming speed; U crit) correlates with metabolic scope (MS) or anaerobic capacity (i.e., maximum EPOC); (3) there is a trade-off between maximum sustained swimming speed (U sus) and minimum cost of transport (COTmin); and (4) variation in U sus correlates positively with optimum swimming speed (U opt; i.e., the speed that minimizes energy expenditure per unit of distance traveled). Data collection involved swimming respirometry and video analysis. Results showed that anaerobic swimming costs (i.e., EPOC) increase linearly with the number of bursts in S. aurata, with each burst corresponding to 0.53 mg O2 kg(-1). Data are consistent with a previous study on striped surfperch (Embiotoca lateralis), a labriform swimmer, suggesting that the metabolic cost of burst swimming is similar across various types of locomotion. There was no correlation between U crit and MS or anaerobic capacity in S. aurata indicating that other factors, including morphological or biomechanical traits, influenced U crit. We found no evidence of a trade-off between U sus and COTmin. In fact, data revealed significant negative correlations between U sus and COTmin, suggesting that individuals with high U sus also exhibit low COTmin. Finally, there were positive correlations between U sus and U opt. Our study demonstrates the energetic importance of anaerobic metabolism during unsteady swimming, and provides intraspecific evidence that superior maximum sustained swimming speed is associated with superior swimming

  14. Swimming by sea otters: adaptations for low energetic cost locomotion.

    PubMed

    Williams, T M

    1989-02-01

    The energetics and hydrodynamics of surface and submerged swimming were compared in the sea otter (Enhydra lutris). 1. Sea otters used two distinct speed ranges that varied with swimming mode. Sustained surface swimming was limited to speeds less than 0.80 m/s, while sustained submerged swimming occurred over the range of 0.60 to 1.39 m/s. 2. Rates of oxygen consumption (VO2) at the transition speed (0.80 m/s) were 41% lower for submerged swimming by sea otters in comparison to surface swimming. 3. Total cost of transport for surface swimming sea otters, 12.56 joules/kg.m, was more than 12 times the predicted value for a similarly-sized salmonid fish. Transport costs for submerged swimming at the same speed was only 7.33 times the predicted value. 4. The allometric relationship for minimum cost of transport in surface swimming birds and mammals was y = 23.87 chi -0.15 where y = cost of transport in joules/kg.m and x = body mass in kg. This regression loosely parallels the relationship for salmonid fish. 5. Correlations between aquatic behavior, morphological specialization, and swimming energetics indicate that the development of swimming in mustelids involved transitions from fore-paw to hind-paw propulsion, and from surface to submerged swimming.

  15. Swimming Eigenworms

    NASA Astrophysics Data System (ADS)

    van Bussel, Frank; Khan, Zeina; Rahman, Mizanur; Vanapalli, Siva; Blawzdziewicz, Jerzy

    2014-03-01

    The nematode C. Elegans is a much studied organism, with a fully mapped genome, cell structure, and nervous system; however, aspects of its behavior have yet to be elucidated, particularly with respect to motility under various conditions. Recently the ``Eigenworm'' technique has emerged as a promising avenue of exploration: via principle component analysis it has been shown that the state space of a healthy crawling worm is low dimensional, in that its shape can be well described by a linear combination of just four eigenmodes. So far, use of this methodology with swimming worms has been somewhat tentative, though medical research such as drug screening is commonly done with nematodes in fluid environments e.g. well plates. Here we give initial results for healthy worms swimming in liquids of varying viscosity. The main result is that at the low viscosities (M9 buffer solution) the state space is even lower dimensional than that for the crawling worm, with only two significant eigenmodes; and that as viscosity increases so does the number of modes needed for an adequate shape description. As well, the shapes of the eigenmodes undergo significant transitions across the range of viscosities looked at.

  16. Swimming Pools for Schools.

    ERIC Educational Resources Information Center

    Neilson, Donald W.; Nixon, John E.

    The increasing interest in swimming instruction and recreation for elementary and secondary school children has resulted in the development of this guide for swimming pool use, design, and construction. Introductory material discussed the need for swimming in the educational program and the organization of swimming programs in the school. Design…

  17. Swimming performance in juvenile shortnose sturgeon (Acipenser brevirostrum): the influence of time interval and velocity increments on critical swimming tests.

    PubMed

    Downie, Adam T; Kieffer, James D

    2017-01-01

    The most utilized method to measure swimming performance of fishes has been the critical swimming speed (UCrit) test. In this test, the fish is forced to swim against an incrementally increasing flow of water until fatigue. Before the water velocity is increased, the fish swims at the water velocity for a specific, pre-arranged time interval. The magnitude of the velocity increments and the time interval for each swimming period can vary across studies making the comparison between and within species difficult. This issue has been acknowledged in the literature, however, little empirical evidence exists that tests the importance of velocity and time increments on swimming performance in fish. A practical application for fish performance is through the design of fishways that enable fish to bypass anthropogenic structures (e.g. dams) that block migration routes, which is one of the causes of world-wide decline in sturgeon populations. While fishways will improve sturgeon conservation, they need to be specifically designed to accommodate the swimming capabilities specific for sturgeons, and it is possible that current swimming methodologies have under-estimated the swimming performance of sturgeons. The present study assessed the UCrit of shortnose sturgeon using modified UCrit to determine the importance of velocity increment (5 and 10 cm s(-1)) and time (5, 15 and 30 min) intervals on swimming performance. UCrit was found to be influenced by both time interval and water velocity. UCrit was generally lower in sturgeon when they were swum using 5cm s(-1) compared with 10 cm s(-1) increments. Velocity increment influences the UCrit more than time interval. Overall, researchers must consider the impacts of using particular swimming criteria when designing their experiments.

  18. Swimming performance in juvenile shortnose sturgeon (Acipenser brevirostrum): the influence of time interval and velocity increments on critical swimming tests

    PubMed Central

    Kieffer, James D.

    2017-01-01

    Abstract The most utilized method to measure swimming performance of fishes has been the critical swimming speed (UCrit) test. In this test, the fish is forced to swim against an incrementally increasing flow of water until fatigue. Before the water velocity is increased, the fish swims at the water velocity for a specific, pre-arranged time interval. The magnitude of the velocity increments and the time interval for each swimming period can vary across studies making the comparison between and within species difficult. This issue has been acknowledged in the literature, however, little empirical evidence exists that tests the importance of velocity and time increments on swimming performance in fish. A practical application for fish performance is through the design of fishways that enable fish to bypass anthropogenic structures (e.g. dams) that block migration routes, which is one of the causes of world-wide decline in sturgeon populations. While fishways will improve sturgeon conservation, they need to be specifically designed to accommodate the swimming capabilities specific for sturgeons, and it is possible that current swimming methodologies have under-estimated the swimming performance of sturgeons. The present study assessed the UCrit of shortnose sturgeon using modified UCrit to determine the importance of velocity increment (5 and 10 cm s−1) and time (5, 15 and 30 min) intervals on swimming performance. UCrit was found to be influenced by both time interval and water velocity. UCrit was generally lower in sturgeon when they were swum using 5cm s−1 compared with 10 cm s−1 increments. Velocity increment influences the UCrit more than time interval. Overall, researchers must consider the impacts of using particular swimming criteria when designing their experiments. PMID:28835841

  19. Effects of intraspecific variation in reproductive traits, pectoral fin use and burst swimming on metabolic rates and swimming performance in the Trinidadian guppy (Poecilia reticulata).

    PubMed

    Svendsen, Jon C; Banet, Amanda I; Christensen, Rune H B; Steffensen, John F; Aarestrup, Kim

    2013-09-15

    There is considerable intraspecific variation in metabolic rates and locomotor performance in aquatic ectothermic vertebrates; however, the mechanistic basis remains poorly understood. Using pregnant Trinidadian guppies (Poecilia reticulata), a live-bearing teleost, we examined the effects of reproductive traits, pectoral fin use and burst-assisted swimming on swimming metabolic rate, standard metabolic rate (O2std) and prolonged swimming performance (Ucrit). Reproductive traits included reproductive allocation and pregnancy stage, the former defined as the mass of the reproductive tissues divided by the total body mass. Results showed that the metabolic rate increased curvilinearly with swimming speed. The slope of the relationship was used as an index of swimming cost. There was no evidence that reproductive traits correlated with swimming cost, O2std or Ucrit. In contrast, data revealed strong effects of pectoral fin use on swimming cost and Ucrit. Poecilia reticulata employed body-caudal fin (BCF) swimming at all tested swimming speeds; however, fish with a high simultaneous use of the pectoral fins exhibited increased swimming cost and decreased Ucrit. These data indicated that combining BCF swimming and pectoral fin movement over a wide speed range, presumably to support swimming stability and control, is an inefficient swimming behaviour. Finally, transition to burst-assisted swimming was associated with an increase in aerobic metabolic rate. Our study highlights factors other than swimming speed that affect swimming cost and suggests that intraspecific diversity in biomechanical performance, such as pectoral fin use, is an important source of variation in both locomotor cost and maximal performance.

  20. Spatial organization and Synchronization in collective swimming of Hemigrammus bleheri

    NASA Astrophysics Data System (ADS)

    Ashraf, Intesaaf; Ha, Thanh-Tung; Godoy-Diana, Ramiro; Thiria, Benjamin; Halloy, Jose; Collignon, Bertrand; Laboratoire de Physique et Mécanique des Milieux Hétérogènes (PMMH) Team; Laboratoire Interdisciplinaire des Energies de Demain (LIED) Team

    2016-11-01

    In this work, we study the collective swimming of Hemigrammus bleheri fish using experiments in a shallow swimming channel. We use high-speed video recordings to track the midline kinematics and the spatial organization of fish pairs and triads. Synchronizations are characterized by observance of "out of phase" and "in phase" configurations. We show that the synchronization state is highly correlated to swimming speed. The increase in synchronization led to efficient swimming based on Strouhal number. In case of fish pairs, the collective swimming is 2D and the spatial organization is characterized by two characteristic lengths: the lateral and longitudinal separation distances between fish pairs.For fish triads, different swimming patterns or configurations are observed having three dimensional structures. We performed 3D kinematic analysis by employing 3D reconstruction using the Direct Linear Transformation (DLT). We show that fish still keep their nearest neighbor distance (NND) constant irrespective of swimming speeds and configuration. We also point out characteristic angles between neighbors, hence imposing preferred patterns. At last we will give some perspectives on spatial organization for larger population. Sorbonne Paris City College of Doctoral Schools. European Union Information and Communication Technologies project ASSISIbf, FP7-ICT-FET-601074.

  1. Mathematical Modeling of Space-Time Variations in Acoustic Transmission and Scattering from Schools of Swim Bladder Fish (FY13 Annual Report)

    DTIC Science & Technology

    2013-09-30

    Santiago, Chile phone: +56 2 354 4800 fax: +56 2 354 4491 email: chris.feuillade@gmail.com Award Number: N00014-111-0161 LONG-TERM GOALS The goal is...the Love swim bladder model is used as the kernel (Ref. 2 ). 1 Report Documentation Page Form ApprovedOMB No. 0704-0188 Public reporting burden for...display a currently valid OMB control number. 1. REPORT DATE 30 SEP 2013 2 . REPORT TYPE 3. DATES COVERED 00-00-2013 to 00-00-2013 4. TITLE AND

  2. A mechanism for efficient swimming

    NASA Astrophysics Data System (ADS)

    Haj-Hariri, Hossein; Saadat, Mehdi; Brandes, Aaron; Saraiya, Vishaal; Bart-Smith, Hilary

    2015-11-01

    We present experimental measurements of hydrodynamic performance as well as wake visualization for a freely swimming 3D foil with pure pitching motion. The foil is constrained to move in its axial direction. It is shown that the iso-lines for speed and input power (or economy) coincide in the dimensional frequency versus amplitude plane, up to a critical amplitude. The critical amplitude is independent from swimming speed. It is shown that all swimming gaits (combination of frequency and amplitude) share a single value for Strouhal number (for amplitudes below the critical amplitude), when plotted in non-dimensional frequency vs. amplitude plane. Additionally, it is shown that the swimming gaits with amplitudes equal to the critical amplitude are energetically superior to others. This finding provides a fundamental mechanism for an important observation made by Bainbridge (1958) namely, most fish (such as trout, dace, goldfish, cod and dolphins) maintain constant tail-beat amplitude during cruise, and their speed is correlated linearly with their tail-beat frequency. The results also support prior findings of Saadat and Haj-Hariri (2013). Supported by ONR MURI Grant N00014-14-1-0533.

  3. Muscle function and swimming in sharks.

    PubMed

    Shadwick, R E; Goldbogen, J A

    2012-04-01

    The locomotor system in sharks has been investigated for many decades, starting with the earliest kinematic studies by Sir James Gray in the 1930s. Early work on axial muscle anatomy also included sharks, and the first demonstration of the functional significance of red and white muscle fibre types was made on spinal preparations in sharks. Nevertheless, studies on teleosts dominate the literature on fish swimming. The purpose of this article is to review the current knowledge of muscle function and swimming in sharks, by considering their morphological features related to swimming, the anatomy and physiology of the axial musculature, kinematics and muscle dynamics, and special features of warm-bodied lamnids. In addition, new data are presented on muscle activation in fast-starts. Finally, recent developments in tracking technology that provide insights into shark swimming performance in their natural environment are highlighted.

  4. Stroke Drills for Swimming Instructors.

    ERIC Educational Resources Information Center

    Cahill, Peter J.

    1982-01-01

    Stroke drills to be used by swimming instructors to teach four competitive swim strokes are described. The drills include: one arm swims; (2) alternative kicks; (3) fist swims; and (4) catch-up strokes. (JN)

  5. Stroke Drills for Swimming Instructors.

    ERIC Educational Resources Information Center

    Cahill, Peter J.

    1982-01-01

    Stroke drills to be used by swimming instructors to teach four competitive swim strokes are described. The drills include: one arm swims; (2) alternative kicks; (3) fist swims; and (4) catch-up strokes. (JN)

  6. An interspecific comparison between morphology and swimming performance in cyprinids.

    PubMed

    Yan, G-J; He, X-K; Cao, Z-D; Fu, S-J

    2013-08-01

    Flow regimes are believed to be of major evolutionary significance in fish. The flow regimes inhabited by cyprinids vary extensively from still flow regimes to riptide flow regimes. To test (i) whether flow-driven swimming performance and relevant morphological differentiation are present among fish species and (ii) whether evolutionary shifts between high-flow and low-flow habitats in cyprinids are associated with evolutionary trade-offs in locomotor performance, we obtained data on both steady and unsteady swimming performance and external body shape for 19 species of cyprinids that typically occur in different flow regimes (still, intermediate and riptide). We also measured the routine energy expenditure (RMR) and maximum metabolic rate (MMR) and calculated the optimal swimming speed. Our results showed that fish species from riptide groups tend to have a higher critical swimming speed (Ucrit ), maximum linear velocity (Vmax ) and fineness ratio (FR) than fish from the other two groups. However, there was no correlation between the reconstructed changes in the steady and unsteady swimming performance of the 19 species. According to the phylogenetically independent contrast (PIC) method, the Ucrit was actively correlated with the MMR. These results indicated that selection will favour both higher steady and unsteady swimming performance and a more streamlined body shape in environments with high water velocities. The results suggested that steady swimming performance was more sensitive to the flow regime and that for this reason, changes in body shape resulted more from selective pressure on steady swimming performance than on unsteady swimming performance. No evolutionary trade-off was observed between steady and unsteady swimming performance, although Ucrit and MMR were found to have coevolved. However, a further analysis within each typically occurring habitat group suggested that the trade-off that may exist between steady and unsteady swimming performance

  7. Teaching Infants to Swim.

    ERIC Educational Resources Information Center

    Barnett, Harvey

    1980-01-01

    The author discusses some of his experiences during the 13 years he has taught handicapped infants to swim. Lessons are usually given for a 10-minute period daily and progress is recorded on a swimming behavior chart. (PHR)

  8. Swimming pool granuloma

    MedlinePlus

    ... this page: //medlineplus.gov/ency/article/001357.htm Swimming pool granuloma To use the sharing features on this page, please enable JavaScript. A swimming pool granuloma is a long-term (chronic) skin ...

  9. Swimming pool cleaner poisoning

    MedlinePlus

    Swimming pool cleaner poisoning occurs when someone swallows this type of cleaner, touches it, or breathes in ... The harmful substances in swimming pool cleaner are: Bromine ... copper Chlorine Soda ash Sodium bicarbonate Various mild acids

  10. 2012 Swimming Season Factsheets

    EPA Pesticide Factsheets

    To help beachgoers make informed decisions about swimming at U.S. beaches, EPA annually publishes state-by-state data about beach closings and advisories for the previous year's swimming season. These fact sheets summarize that information by state.

  11. Swimming Pool Safety

    MedlinePlus

    ... closing/self-latching Window guards Pool alarms Swimming Lessons - Where We Stand Children need to learn to ... Some factors you may consider before starting swimming lessons for younger children include: Frequency of exposure to ...

  12. Modeling of breaststroke swimming

    NASA Astrophysics Data System (ADS)

    Karmanov, S. P.; Chernous'ko, F. L.

    2014-02-01

    A mechanical system that models swimming using a pair of two-chain extremities is considered. The motion of the system under study is similar to swimming of a frog and some other animals, in which lower extremities play the main role. This type of motion is characteristic of competitive breaststroke swimming.

  13. Effects of feeding on the sustained swimming abilities of late-stage larval Amphiprion melanopus

    NASA Astrophysics Data System (ADS)

    Fisher, R.; Bellwood, D.

    2001-09-01

    To date, all sustained swimming experiments on tropical reef fish larvae have been conducted using unfed larvae. Such studies may produce unrealistic estimates of sustained swimming abilities. We examined the effect of food on the sustained swimming ability of late-stage Amphiprion melanopus. Larvae were swum in a six-channel swimming flume at 7 cm s-1, with "unfed" and "fed" channels. Fed channels had Artemia nauplii added four times per day for 10 min. Feeding larvae during swimming experiments significantly increased their average swimming distance from around 6.9 to 12.2 km, and the maximum swimming distance from around 11.8 to 28.7 km. Existing flume-based estimates of sustained swimming may be underestimating field abilities. With access to food, many larvae may have the potential to swim considerably greater distances than previously suggested.

  14. Optimization of Anguilliform Swimming

    NASA Astrophysics Data System (ADS)

    Kern, Stefan; Koumoutsakos, Petros

    2006-03-01

    Anguilliform swimming is investigated by 3D computer simulations coupling the dynamics of an undulating eel-like body with the surrounding viscous fluid flow. The body is self-propelled and, in contrast to previous computational studies of swimming, the motion pattern is not prescribed a priori but obtained by an evolutionary optimization procedure. Two different objective functions are used to characterize swimming efficiency and maximum swimming velocity with limited input power. The found optimal motion patterns represent two distinct swimming modes corresponding to migration, and burst swimming, respectively. The results support the hypothesis from observations of real animals that eels can modify their motion pattern generating wakes that reflect their propulsive mode. Unsteady drag and thrust production of the swimming body are thoroughly analyzed by recording the instantaneous fluid forces acting on partitions of the body surface.

  15. Limit cycle dynamics in swimming systems

    NASA Astrophysics Data System (ADS)

    Finkel, Cyndee; von Ellenrieder, Karl

    2013-11-01

    An experimental apparatus was constructed to model basic features expected in the flow about a freely swimming fish. A D-shaped cylinder is used to represent the body and an oscillating foil, the tail. The swimming system is suspended in a constant freestream flow. A closed loop PI controller is used to maintain a set point, stream-wise location. The system is released from multiple downstream and upstream locations and permitted to swim to the set point. The Strouhal number measured when the swimming system achieves a constant forward swimming speed is compared to values observed in nature. The results suggest that self-regulation passively selects the Strouhal number and that no other external sensory input is necessary for this to happen. This self-regulation is a result of a limit cycle process that stems from nonlinear periodic oscillations. Phase plane analyses are used to examine the synchronous conditions due to the coupling of the foil and wake vortices. It is shown that the phase locking indices depend on the Strouhal number and approach a frequency locking ratio of about 0 . 5 . The results suggest that Strouhal number selection in steady forward natural swimming is the result of a limit cycle process and not actively controlled by an organism.

  16. Energetics of median and paired fin swimming, body and caudal fin swimming, and gait transition in parrotfish (Scarus schlegeli) and triggerfish (Rhinecanthus aculeatus).

    PubMed

    Korsmeyer, Keith E; Steffensen, John Fleng; Herskin, Jannik

    2002-05-01

    To determine the energetic costs of rigid-body, median or paired-fin (MPF) swimming versus undulatory, body-caudal fin (BCF) swimming, we measured oxygen consumption as a function of swimming speed in two MPF swimming specialists, Schlegel's parrotfish and Picasso triggerfish. The parrotfish swam exclusively with the pectoral fins at prolonged swimming speeds up to 3.2 total lengths per second (L s(-1); 30 min critical swimming speed, U(crit)). At higher speeds, gait transferred to a burst-and-coast BCF swimming mode that resulted in rapid fatigue. The triggerfish swam using undulations of the soft dorsal and anal fins up to 1.5 L s(-1), beyond which BCF undulations were recruited intermittently. BCF swimming was used continuously above 3.5 L s(-1), and was accompanied by synchronous undulations of the dorsal and anal fins. The triggerfish were capable of high, prolonged swimming speeds of up to 4.1 L s(-1) (30 min U(crit)). In both species, the rates of increase in oxygen consumption with swimming speed were higher during BCF swimming than during rigid-body MPF swimming. Our results indicate that, for these species, undulatory swimming is energetically more costly than rigid-body swimming, and therefore support the hypothesis that MPF swimming is more efficient. In addition, use of the BCF gait at higher swimming speed increased the cost of transport in both species beyond that predicted for MPF swimming at the same speeds. This suggests that, unlike for terrestrial locomotion, gait transition in fishes does not occur to reduce energetic costs, but to increase recruitable muscle mass and propulsive surfaces. The appropriate use of the power and exponential functions to model swimming energetics is also discussed.

  17. Cetacean Swimming with Prosthetic Limbs

    NASA Astrophysics Data System (ADS)

    Bode-Oke, Ayodeji; Ren, Yan; Dong, Haibo; Fish, Frank

    2016-11-01

    During entanglement in fishing gear, dolphins can suffer abrasions and amputations of flukes and fins. As a result, if the dolphin survives the ordeal, swimming performance is altered. Current rehabilitation technques is the use of prosthesis to regain swimming ability. In this work, analyses are focused on two dolphins with locomotive impairment; Winter (currently living in Clearwater Marine Aquarium in Florida) and Fuji (lived in Okinawa Churaumi Aquarium in Japan). Fuji lost about 75% of its fluke surface to necrosis (death of cells) and Winter lost its tail due to amputation. Both dolphins are aided by prosthetic tails that mimic the shape of a real dolphin tail. Using 3D surface reconstruction techniques and a high fidelity Computational Fluid Dynamics (CFD) flow solver, we were able to elucidate the kinematics and hydrodynamics and fluke deformation of these swimmers to clarify the effectiveness of prostheses in helping the dolphins regain their swimming ability. Associated with the performance, we identified distinct features in the wake structures that can explain this gap in the performance compared to a healthy dolphin. This work was supported by ONR MURI Grant Number N00014-14-1-0533.

  18. Dead fish swimming: a review of research on the early migration and high premature mortality in adult Fraser River sockeye salmon Oncorhynchus nerka.

    PubMed

    Hinch, S G; Cooke, S J; Farrell, A P; Miller, K M; Lapointe, M; Patterson, D A

    2012-07-01

    Adult sockeye salmon Oncorhynchus nerka destined for the Fraser River, British Columbia are some of the most economically important populations but changes in the timing of their homeward migration have led to management challenges and conservation concerns. After a directed migration from the open ocean to the coast, this group historically would mill just off shore for 3-6 weeks prior to migrating up the Fraser River. This milling behaviour changed abruptly in 1995 and thereafter, decreasing to only a few days in some years (termed early migration), with dramatic consequences that have necessitated risk-averse management strategies. Early migrating fish consistently suffer extremely high mortality (exceeding 90% in some years) during freshwater migration and on spawning grounds prior to spawning. This synthesis examines multidisciplinary, collaborative research aimed at understanding what triggers early migration, why it results in high mortality, and how fisheries managers can utilize these scientific results. Tissue analyses from thousands of O. nerka captured along their migration trajectory from ocean to spawning grounds, including hundreds that were tracked with biotelemetry, have revealed that early migrants are more reproductively advanced and ill-prepared for osmoregulatory transition upon their entry into fresh water. Gene array profiles indicate that many early migrants are also immunocompromised and stressed, carrying a genomic profile consistent with a viral infection. The causes of these physiological changes are still under investigation. Early migration brings O. nerka into the river when it is 3-6° C warmer than historical norms, which for some late-run populations approaches or exceeds their critical maxima leading to the collapse of metabolic and cardiac scope, and mortality. As peak spawning dates have not changed, the surviving early migrants tend to mill in warm lakes near to spawning areas. These results in the accumulation of many more

  19. The Complex Hydrodynamics of Swimming in the Spanish Dancer

    NASA Astrophysics Data System (ADS)

    Zhou, Zhuoyu; Mittal, Rajat

    2016-11-01

    The lack of a vertebra seems to have freed marine gastropods to explore and exploit a stupendous variety of swimming kinematics. In fact, examination of just a few animals in this group reveal locomotory modes ranging from insect-like flapping, to fish-like undulatory swimming, jet propulsion, and rajiform (manta-like) swimming. There are also a number of marine gastropods that have bizarre swimming gaits with no equivalent among fish or marine mammals. In this latter category is the Spanish Dancer (Hexabranchus sanguineus) a sea slug that swims with a complex combination of body undulations and flapping parapodia. While the neurobiology of these animals has been relatively well-studied, less is known about their propulsive mechanism and swimming energetics. In this study, we focus on the hydrodynamics of two distinct swimmers: the Spanish Dancer, and the sea hare Aplysia; the latter adopts a rajiform-like mode of swimming by passing travelling waves along its parapodia. In the present study an immersed boundary method is employed to examine the vortex structures, hydrodynamic forces and energy costs of the swimming in these animals. NSF Grant No. 1246317.

  20. Swimming and the heart.

    PubMed

    Lazar, Jason M; Khanna, Neel; Chesler, Roseann; Salciccioli, Louis

    2013-09-20

    Exercise training is accepted to be beneficial in lowering morbidity and mortality in patients with cardiac disease. Swimming is a popular recreational activity, gaining recognition as an effective option in maintaining and improving cardiovascular fitness. Swimming is a unique form of exercise, differing from land-based exercises such as running in many aspects including medium, position, breathing pattern, and the muscle groups used. Water immersion places compressive forces on the body with resulting physiologic effects. We reviewed the physiologic effects and cardiovascular responses to swimming, the cardiac adaptations to swim training, swimming as a cardiac disease risk factor modifier, and the effects of swimming in those with cardiac disease conditions such as coronary artery disease, congestive heart failure and the long-QT syndrome.

  1. Applied physiology of swimming.

    PubMed

    Lavoie, J M; Montpetit, R R

    1986-01-01

    Scientific research in swimming over the past 10 to 15 years has been oriented toward multiple aspects that relate to applied and basic physiology, metabolism, biochemistry, and endocrinology. This review considers recent findings on: 1) specific physical characteristics of swimmers; 2) the energetics of swimming; 3) the evaluation of aerobic fitness in swimming; and 4) some metabolic and hormonal aspects related to swimmers. Firstly, the age of finalists in Olympic swimming is not much different from that of the participants from other sports. They are taller and heavier than a reference population of the same age. The height bias in swimming may be the reason for lack of success from some Asian and African countries. Experimental data point toward greater leanness, particularly in female swimmers, than was seen 10 years ago. Overall, female swimmers present a range of 14 to 19% body fat whereas males are much lower (5 to 10%). Secondly, the relationship between O2 uptake and crawl swimming velocity (at training and competitive speeds) is thought to be linear. The energy cost varies between strokes with a dichotomy between the 2 symmetrical and the 2 asymmetrical strokes. Energy expenditure in swimming is represented by the sum of the cost of translational motion (drag) and maintenance of horizontal motion (gravity). The cost of the latter decreases as speed increases. Examination of the question of size-associated effects on the cost of swimming using Huxley's allometric equation (Y = axb) shows an almost direct relationship with passive drag. Expressing energy cost in litres of O2/m/kg is proposed as a better index of technical swimming ability than the traditional expression of VO2/distance in L/km. Thirdly, maximal direct conventional techniques used to evaluate maximal oxygen consumption (VO2 max) in swimming include free swimming, tethered swimming, and flume swimming. Despite the individual peculiarities of each method, with similar experimental conditions

  2. Fish under exercise.

    PubMed

    Palstra, Arjan P; Planas, Josep V

    2011-06-01

    Improved knowledge on the swimming physiology of fish and its application to fisheries science and aquaculture (i.e., farming a fitter fish) is currently needed in the face of global environmental changes, high fishing pressures, increased aquaculture production as well as increased concern on fish well-being. Here, we review existing data on teleost fish that indicate that sustained exercise at optimal speeds enhances muscle growth and has consequences for flesh quality. Potential added benefits of sustained exercise may be delay of ovarian development and stimulation of immune status. Exercise could represent a natural, noninvasive, and economical approach to improve growth, flesh quality as well as welfare of aquacultured fish: a FitFish for a healthy consumer. All these issues are important for setting directions for policy decisions and future studies in this area. For this purpose, the FitFish workshop on the Swimming Physiology of Fish ( http://www.ub.edu/fitfish2010 ) was organized to bring together a multidisciplinary group of scientists using exercise models, industrial partners, and policy makers. Sixteen international experts from Europe, North America, and Japan were invited to present their work and view on migration of fishes in their natural environment, beneficial effects of exercise, and applications for sustainable aquaculture. Eighty-eight participants from 19 different countries contributed through a poster session and round table discussion. Eight papers from invited speakers at the workshop have been contributed to this special issue on The Swimming Physiology of Fish.

  3. Effect of temperature on swimming performance of juvenile Schizothorax prenanti.

    PubMed

    Cai, Lu; Liu, Guoyong; Taupier, Rachel; Fang, Min; Johnson, David; Tu, Zhiying; Huang, Yingping

    2014-04-01

    The migration of Schizothorax prenanti, an ecologically important and commercially valuable species, is impeded by dams. Effective fishways would contribute to conservation of wild populations, and swimming performance data are necessary for fishway design. The swimming performance of S. prenanti was investigated at four temperatures (15, 19, 23, 27 °C), and numerical models were used to characterize the effect of temperature on swimming performance. As temperature increases, critical swimming speed (U crit) increases from 15 to 23 °C and then decreases significantly. The highest U crit (7.71 BL/s) occurs at 24 °C, as estimated by interpolation. Swimming efficiency was similar from 19 to 23 °C, but decreases significantly at 27 °C. The temperature range 15-23 °C is suitable for S. prenanti. However, the excess post-exercise oxygen consumption values of Q 10 for the four temperature increments indicate that 19-23 °C is the optimal range for swimming performance. Maximum tail beat amplitude increased >25 % (0.35-0.45 BL) over the temperature range considered, but variation of tail beat frequency was erratic. White muscle fiber begins to contribute to swimming at swimming speeds ~40 % U crit at the lower three temperatures, but increases to almost 60 % at 27 °C, and the contribution is relatively small. The results of this investigation advance the knowledge of fish metabolism while swimming provides data critical for fishway design.

  4. An integrative CFD model of lamprey swimming

    NASA Astrophysics Data System (ADS)

    Hsu, Chia-Yu; McMillen, Tyler; Fauci, Lisa

    2008-11-01

    Swimming due to sinusoidal body undulations is observed across the full spectrum of swimming organisms, from microscopic flagella to fish. These undulations are achieved due to internal force-generating mechanisms, which, in the case of lamprey are due to a wave of neural activation from head to tail which gives rise to a wave of muscle activation. These active forces are also mediated by passive structural forces. Here we present recent results on a computational model of a swimming lamprey that couples activation of discrete muscle segments, passive elastic forces, and a surrounding viscous, incompressible fluid. The fluid dynamics is modeled by the Navier-Stokes equations at appropriate Reynolds numbers, where the resulting flow field and vortex shedding may be measured.

  5. Volumetric flow around a swimming lamprey

    NASA Astrophysics Data System (ADS)

    Lehn, Andrea M.; Colin, Sean P.; Costello, John H.; Leftwich, Megan C.; Tytell, Eric D.

    2015-11-01

    A primary experimental technique for studying fluid-structure interactions around swimming fish has been planar dimensional particle image velocimetry (PIV). Typically, two components of the velocity vector are measured in a plane, in the case of swimming studies, directly behind the animal. While useful, this approach provides little to no insight about fluid structure interactions above and below the fish. For fish with a small height relative to body length, such as the long and approximately cylindrical lamprey, 3D information is essential to characterize how these fish interact with their fluid environment. This study presents 3D flow structures along the body and in the wake of larval lamprey, P etromyzon m arinus , which are 10-15 cm long. Lamprey swim through a 1000 cm3 field of view in a standard 10 gallon tank illuminated by a green laser. Data are collected using the three component velocimeter V3V system by TSI, Inc. and processed using Insight 4G software. This study expands on previous works that show two pairs of vortices each tail beat in the mid-plane of the lamprey wake. NSF DMS 1062052.

  6. Swimming performance of biomimetic trapezoidal elastic fins

    NASA Astrophysics Data System (ADS)

    Spadaro, Michael; Yeh, Peter; Alexeev, Alexander

    2016-11-01

    Using three-dimensional computer simulations, we probe the biomimetic free-swimming of trapezoidal elastic plates plunging sinusoidally in a viscous fluid, varying the frequency of oscillations and plate geometry. We choose the elastic trapezoidal plate geometry because it more closely approximates the shape of real caudal fish fins. Indeed, caudal fins are found in nature in a variety of trapezoidal shapes with different aspect ratios. Because of this, we perform our simulations using plates with aspect ratios varying from the cases where the plate has a longer leading edge and to plates with a longer trailing edge. We find that the trapezoidal fins with the longer trailing edge are less efficient than the rectangular fins at the equivalent oscillation frequencies. This is surprising because many fish found in nature have a widening tail. We relate this to the fact that our model considers fins with uniform thickness whereas fish uses tapered fins. Our results will be useful for the design of biomimetic swimming devices as well as understanding more closely the physics of fish swimming.

  7. Teach Your Child Swimming.

    ERIC Educational Resources Information Center

    Gorton, B.E.

    This illustrated guide provides basic knowledge that will enable parents to teach their children to swim, starting from the first visit to the pool up to the development of higher water skills. All the main swimming strokes are dealt with, and the appropriate teaching stages are described. The teaching of starts and turns for each stroke and other…

  8. Teaching Swimming Effectively.

    ERIC Educational Resources Information Center

    Larrabee, Jean G.

    A step-by-step sequential plan is offered for developing a successful competitive swimming season, including how to teach swimming strokes and organize practices. Various strokes are analyzed, and coaching check points are offered along with practice drills, helpful hints on proper body positioning, arm strokes, kicking patterns, breathing…

  9. Teaching Swimming Effectively.

    ERIC Educational Resources Information Center

    Larrabee, Jean G.

    A step-by-step sequential plan is offered for developing a successful competitive swimming season, including how to teach swimming strokes and organize practices. Various strokes are analyzed, and coaching check points are offered along with practice drills, helpful hints on proper body positioning, arm strokes, kicking patterns, breathing…

  10. Elastic swimming I: Optimization

    NASA Astrophysics Data System (ADS)

    Lauga, Eric; Yu, Tony; Hosoi, Anette

    2006-03-01

    We consider the problem of swimming at low Reynolds number by oscillating an elastic filament in a viscous liquid, as investigated by Wiggins and Goldstein (1998, Phys Rev Lett). In this first part of the study, we characterize the optimal forcing conditions of the swimming strategy and its optimal geometrical characteristics.

  11. Flapping flexible fish

    NASA Astrophysics Data System (ADS)

    Root, Robert G.; Courtland, Hayden-William; Shepherd, William; Long, John H.

    In order to analyze and model the body kinematics used by fish in a wide range of swimming behaviors, we developed a technique to separate the periodic whole-body motions that characterize steady swimming from the secular motions that characterize changes in whole-body shape. We applied this harmonic analysis technique to the study of the forward and backward swimming of lamprey. We found that in order to vary the unsteadiness of swimming, lamprey superimpose periodic and secular components of their body motion, modulate the patterns and magnitudes of those components, and change shape. These kinematic results suggest the following hydromechanical hypothesis: steady swimming is a maneuver that requires active suppression of secular body reconfigurations.

  12. The effects of low-speed swimming following exhaustive exercise on metabolic recovery and swimming performance in brook trout (Salvelinus fontinalis).

    PubMed

    Kieffer, James D; Kassie, Roshini S; Taylor, Susan G

    2011-01-01

    Experiments were conducted to determine whether low-speed swimming during recovery from exhaustive exercise improved both metabolic recovery and performance during a swimming challenge. For these experiments, brook trout were allowed to recover from exhaustive exercise for 2 h while swimming at 0, 0.5, 1.0, or 1.5 body length (BL) s(-1) or allowed to recover from exhaustive exercise for 1, 2, or 3 h while swimming at 1.0 BL s(-1). At the appropriate interval, either (i) muscle and blood samples were removed from the fish or (ii) fish were assessed for performance (i.e., fatigue time) during a fixed-interval swimming test. Low-speed swimming during recovery from exhaustive exercise resulted in significantly longer fatigue times compared with fish recovering in still water (i.e., 0 BL s(-1)). However, swimming during recovery did not expedite recovery of muscle lactate or blood variables (e.g., lactate, osmolarity, glucose). These observations suggest that metabolic recovery and subsequent swimming performance may not be directly linked and that other factors play a role in swimming recovery in brook trout.

  13. Altered burst swimming in rainbow trout Oncorhynchus mykiss exposed to natural and synthetic oestrogens.

    PubMed

    Osachoff, H L; Osachoff, K N; Wickramaratne, A E; Gunawardane, E K; Venturini, F P; Kennedy, C J

    2014-08-01

    Juvenile rainbow trout Oncorhynchus mykiss were exposed to two concentrations each of 17β-oestradiol (E2; natural oestrogen hormone) or 17α-ethinyl oestradiol (EE2; a potent synthetic oestrogen hormone) to evaluate their potential effects on burst-swimming performance. In each of six successive burst-swimming assays, burst-swimming speed (Uburst ) was lower in fish exposed to 0.5 and 1 µg l(-1) E2 and EE2 for four days compared with control fish. A practice swim (2 days prior to exposure initiation) in control fish elevated initial Uburst values, but this training effect was not evident in the 1 µg l(-1) EE2-exposed fish. Several potential oestrogen-mediated mechanisms for Uburst reductions were investigated, including effects on metabolic products, osmoregulation and blood oxygen-carrying capacity. Prior to burst-swimming trials, fish exposed to E2 and EE2 for 4 days had significantly reduced erythrocyte numbers and lower plasma glucose concentrations. After six repeated burst-swimming trials, plasma glucose, lactate and creatinine concentrations were not significantly different among treatment groups; however, plasma Cl(-) concentrations were significantly reduced in E2- and EE2-treated fish. In summary, E2 and EE2 exposure altered oxygen-carrying capacity ([erythrocytes]) and an osmoregulatory-related variable ([Cl(-) ]), effects that may underlie reductions in burst-swimming speed, which will have implications for fish performance in the wild.

  14. Swimming near the substrate: a simple robotic model of stingray locomotion.

    PubMed

    Blevins, Erin; Lauder, George V

    2013-03-01

    Studies of aquatic locomotion typically assume that organisms move through unbounded fluid. However, benthic fishes swim close to the substrate and will experience significant ground effects, which will be greatest for fishes with wide spans such as benthic batoids and flatfishes. Ground effects on fixed-wing flight are well understood, but these models are insufficient to describe the dynamic interactions between substrates and undulating, oscillating fish. Live fish alter their swimming behavior in ground effect, complicating comparisons of near-ground and freestream swimming performance. In this study, a simple, stingray-inspired physical model offers insights into ground effects on undulatory swimmers, contrasting the self-propelled swimming speed, power requirements, and hydrodynamics of fins swimming with fixed kinematics near and far from a solid boundary. Contrary to findings for gliding birds and other fixed-wing fliers, ground effect does not necessarily enhance the performance of undulating fins. Under most kinematic conditions, fins do not swim faster in ground effect, power requirements increase, and the cost of transport can increase by up to 10%. The influence of ground effect varies with kinematics, suggesting that benthic fish might modulate their swimming behavior to minimize locomotor penalties and incur benefits from swimming near a substrate.

  15. Analysis of swimming motions.

    NASA Technical Reports Server (NTRS)

    Gallenstein, J.; Huston, R. L.

    1973-01-01

    This paper presents an analysis of swimming motion with specific attention given to the flutter kick, the breast-stroke kick, and the breast stroke. The analysis is completely theoretical. It employs a mathematical model of the human body consisting of frustrums of elliptical cones. Dynamical equations are written for this model including both viscous and inertia forces. These equations are then applied with approximated swimming strokes and solved numerically using a digital computer. The procedure is to specify the input of the swimming motion. The computer solution then provides the output displacement, velocity, and rotation or body roll of the swimmer.

  16. Analysis of swimming motions.

    NASA Technical Reports Server (NTRS)

    Gallenstein, J.; Huston, R. L.

    1973-01-01

    This paper presents an analysis of swimming motion with specific attention given to the flutter kick, the breast-stroke kick, and the breast stroke. The analysis is completely theoretical. It employs a mathematical model of the human body consisting of frustrums of elliptical cones. Dynamical equations are written for this model including both viscous and inertia forces. These equations are then applied with approximated swimming strokes and solved numerically using a digital computer. The procedure is to specify the input of the swimming motion. The computer solution then provides the output displacement, velocity, and rotation or body roll of the swimmer.

  17. PFOS affects posterior swim bladder chamber inflation and swimming performance of zebrafish larvae.

    PubMed

    Hagenaars, A; Stinckens, E; Vergauwen, L; Bervoets, L; Knapen, D

    2014-12-01

    Perfluorooctane sulphonate (PFOS) is one of the most commonly detected perfluorinated alkylated substances in the aquatic environment due to its persistence and the degradation of less stable compounds to PFOS. PFOS is known to cause developmental effects in fish. The main effect of PFOS in zebrafish larvae is an uninflated swim bladder. As no previous studies have focused on the effect of PFOS on zebrafish swim bladder inflation, the exact mechanisms leading to this effect are currently unknown. The objective of this study was to determine the exposure windows during early zebrafish development that are sensitive to PFOS exposure and result in impaired swim bladder inflation in order to specify the mechanisms by which this effect might be caused. Seven different time windows of exposure (1-48, 1-72, 1-120, 1-144, 48-144, 72-144, 120-144h post fertilization (hpf)) were tested based on the different developmental stages of the swim bladder. These seven time windows were tested for four concentrations corresponding to the EC-values of 1, 10, 80 and 95% impaired swim bladder inflation (EC1=0.70 mg L(-1), EC10=1.14 mg L(-1), EC80=3.07 mg L(-1) and EC95=4.28 mg L(-1)). At 6 days post fertilization, effects on survival, hatching, swim bladder inflation and size, larval length and swimming performance were assessed. For 0.70 mg L(-1), no significant effects were found for the tested parameters while 1.14 mg L(-1) resulted in a reduction of larval length. For 3.07 and 4.28 mg L(-1), the number of larvae affected and the severity of effects caused by PFOS were dependent on the time window of exposure. Exposure for 3 days or more resulted in significant reductions of swim bladder size, larval length and swimming speed with increasing severity of effects when the duration of exposure was longer, suggesting a possible effect of accumulated dose. Larvae that were only exposed early (1-48 hpf) or late (120-144 hpf) during development showed no effects on the studied endpoints

  18. Strouhal number for free swimming

    NASA Astrophysics Data System (ADS)

    Saadat, Mehdi; van Buren, Tyler; Floryan, Daniel; Smits, Alexander; Haj-Hariri, Hossein

    2015-11-01

    In this work, we present experimental results to explore the implications of free swimming for Strouhal number (as an outcome) in the context of a simple model for a fish that consists of a 2D virtual body (source of drag) and a 2D pitching foil (source of thrust) representing cruising with thunniform locomotion. The results validate the findings of Saadat and Haj-Hariri (2012): for pitching foils thrust coefficient is a function of Strouhal number for all gaits having amplitude less than a certain critical value. Equivalently, given the balance of thrust and drag forces at cruise, Strouhal number is only a function of the shape, i.e. drag coefficient and area, and essentially a constant for high enough swimming speeds for which the mild dependence of drag coefficient on the speed vanishes. Furthermore, a dimensional analysis generalizes the findings. A scaling analysis shows that the variation of Strouhal number with cruising speed is functionally related to the variation of body drag coefficient with speed. Supported by ONR MURI Grant N00014-14-1-0533.

  19. Bacteria swimming in circles

    NASA Astrophysics Data System (ADS)

    Lauga, Eric; Diluzio, Willow; Garstecki, Piotr; Whitesides, George; Stone, Howard

    2004-11-01

    The bacteria E.coli, which lives in our stomach, swims in a viscous fluid by rotating its flagella together in a helical bundle. The rotation is due to the action of rotary motors embedded in the cell wall. Motivated by experimental observations (Frymier et al., 1995, PNAS vol. 92), as well as our own extensive experiments, that bacteria near solid surfaces do not swim in a straight line but swim in circles, we present a mechanical model for a swimming microorganism near a solid boundary. We show that the combination of a rotating helical bundle and a solid boundary leads to a circular motion to the right of the bacterium (as viewed from above), in accordance with experimental observations. Values of the radii of the circle and the rotation rate are predicted and compared with experimental data.

  20. Saturday Afternoon Swim

    NASA Image and Video Library

    2014-06-29

    Hours after the June 28, 2014, test of NASA Low-Density Supersonic Decelerator over the U.S. Navy Pacific Missile Range, two members of the Navy Explosive Ordinance Disposal swim toward the test vehicle.

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

    PubMed

    Goertzen, Meghan M; Hauck, Dominic W; Phibbs, James; Weber, Lynn P; Janz, David M

    2012-01-01

    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

  2. Swimming performance of young lake trout after chronic exposure to PCBs and DDE

    USGS Publications Warehouse

    Rottiers, Donald V.; Bergstedt, Roger A.

    1981-01-01

    Swimming performance was measured in fry of lake trout (Salvelinus namaycush) exposed to PCB's, DDE, and a combination of these two contaminants in both food and water at concentrations equal to, and 5 and 25 times higher than, levels found in Lake Michigan water and plankton. Fry were tested after about 50, 110, and 165 days of exposure. We measured swimming performance by forcing the fry to swim through a continuous series of incrementally increased velocities until the fish were exhausted. Although we observed significant differences in swimming performance between a few test groups, we detected no relation between swimming performance of the fry and exposure to PCB's or DDE, or both, at the concentrations tested. Inasmuch as swimming performance apparently was not affected by the levels of contamination by PCB's and DDE in Lake Michigan, impairment of swimming by these contaminants cannot account for the failure of lake trout reproduction in Lake Michigan.

  3. [Swimming-induced asthma].

    PubMed

    Fjellbirkeland, L; Gulsvik, A; Walløe, A

    1995-06-30

    Swimming is said to have low asthmogeneity especially when compared with other physical activities. Four young athletes who participated in heavy swimming exercise are reported as having symptoms of exercise-induced asthma (EIA). Three of them started to develop the symptoms after several years of training and had no former history of asthma. In the fourth, the asthma was diagnosed in childhood but the EIA-symptoms here exacerbated by swimming. All four experienced more symptoms when the air in the swimming pool was warm, or when there was a strong smell of chlorine. Two of the athletes reported having no symptoms when they swam in outdoor pools and had only minor symptoms, or none at all, when they did other formes of physical exercise, including running. In all four their swimming performance was hampered by their respiratory symptoms. Two of the swimmers improved when they inhaled steroids and adrenerg-beta 2 agonists, and continued their swimming carrier. The cases suggest that an irritant may provoke asthma symptoms in susceptible swimmers. Volatile compounds from chlorination of the pools are suspected as possible irritant agents.

  4. Intermittent Swimming with a Flexible Propulsor

    NASA Astrophysics Data System (ADS)

    Akoz, Emre; Zeyghami, Samane; Moored, Keith

    2016-11-01

    Some animals propel themselves by using an intermittent swimming gait known as a burst-and-glide or a burst-and-coast motion. These swimmers tend to have a more pronounced pitching of their caudal fins than heaving leading to low non-dimensional heave-to-pitch ratios. Recent work has shown that when this ratio is sufficiently low the efficiency of an intermittently heaving/pitching airfoil can be significantly improved over a continuously oscillating airfoil. However, fish that swim with an intermittent gait, such as cod and saithe, do not have rigid fins, but instead have highly flexible fins. To examine the performance and flow structures of an intermittent swimmer with a flexible propulsor, a fast boundary element method solver strongly coupled with a torsional-spring structural model was developed. A self-propelled virtual body combined with a flexible-hinged pitching airfoil is used to model a free-swimming animal and its flexible caudal fin. The duty cycle of the active to the coasting phase of motion, the torsional spring flexibility and the forcing frequency are all varied. The cost-of-transport and the swimming speed are measured and connected to the observed wake patterns. Supported by the Office of Naval Research under Program Director Dr. Bob Brizzolara, MURI Grant Number N00014-14-1-0533.

  5. Swimming behaviour of juvenile Pacific lamprey, Lampetra tridentata

    SciTech Connect

    Dauble, Dennis D.; Moursund, Russell A.; Bleich, Matthew D.

    2006-02-01

    Actively migrating juvenile Pacific lamprey (Lampetra tridentata Richardson, 1836) were collected from hydroelectric bypass facilities in the Columbia River and transferred to the laboratory to study their diel movement patterns and swimming ability. Volitional movement of lamprey was restricted mainly to night, with 94% of all swimming activity occurring during the 12-hr dark period. Burst speed of juvenile lamprey ranged from 56 to 94 cm/s with a mean of 71 ±5 cm/s or an average speed of 5.2 body lengths (BL)/s. Sustained swim speed for 5-min test intervals ranged from 0 to 46 cm/s with a median of 23 cm/s. Critical swimming speed was 36.0±10.0 cm/s and 2.4±0.6 BL/s. There was no significant relationship between fish length and critical swimming speed. Overall swimming performance of juvenile Pacific lamprey is low compared to that of most anadromous teleosts. Their poor swimming ability provides a challenge during the freshwater migration interval to the Pacific Ocean.

  6. Optimal shape and motion of undulatory swimming organisms.

    PubMed

    Tokić, Grgur; Yue, Dick K P

    2012-08-07

    Undulatory swimming animals exhibit diverse ranges of body shapes and motion patterns and are often considered as having superior locomotory performance. The extent to which morphological traits of swimming animals have evolved owing to primarily locomotion considerations is, however, not clear. To shed some light on that question, we present here the optimal shape and motion of undulatory swimming organisms obtained by optimizing locomotive performance measures within the framework of a combined hydrodynamical, structural and novel muscular model. We develop a muscular model for periodic muscle contraction which provides relevant kinematic and energetic quantities required to describe swimming. Using an evolutionary algorithm, we performed a multi-objective optimization for achieving maximum sustained swimming speed U and minimum cost of transport (COT)--two conflicting locomotive performance measures that have been conjectured as likely to increase fitness for survival. Starting from an initial population of random characteristics, our results show that, for a range of size scales, fish-like body shapes and motion indeed emerge when U and COT are optimized. Inherent boundary-layer-dependent allometric scaling between body mass and kinematic and energetic quantities of the optimal populations is observed. The trade-off between U and COT affects the geometry, kinematics and energetics of swimming organisms. Our results are corroborated by empirical data from swimming animals over nine orders of magnitude in size, supporting the notion that optimizing U and COT could be the driving force of evolution in many species.

  7. Optimal shape and motion of undulatory swimming organisms

    PubMed Central

    Tokić, Grgur; Yue, Dick K. P.

    2012-01-01

    Undulatory swimming animals exhibit diverse ranges of body shapes and motion patterns and are often considered as having superior locomotory performance. The extent to which morphological traits of swimming animals have evolved owing to primarily locomotion considerations is, however, not clear. To shed some light on that question, we present here the optimal shape and motion of undulatory swimming organisms obtained by optimizing locomotive performance measures within the framework of a combined hydrodynamical, structural and novel muscular model. We develop a muscular model for periodic muscle contraction which provides relevant kinematic and energetic quantities required to describe swimming. Using an evolutionary algorithm, we performed a multi-objective optimization for achieving maximum sustained swimming speed U and minimum cost of transport (COT)—two conflicting locomotive performance measures that have been conjectured as likely to increase fitness for survival. Starting from an initial population of random characteristics, our results show that, for a range of size scales, fish-like body shapes and motion indeed emerge when U and COT are optimized. Inherent boundary-layer-dependent allometric scaling between body mass and kinematic and energetic quantities of the optimal populations is observed. The trade-off between U and COT affects the geometry, kinematics and energetics of swimming organisms. Our results are corroborated by empirical data from swimming animals over nine orders of magnitude in size, supporting the notion that optimizing U and COT could be the driving force of evolution in many species. PMID:22456876

  8. Swimming pool. View of aisle between swimming pool and seating ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    Swimming pool. View of aisle between swimming pool and seating area. Non-original spa pool is partially visible on right. - Jewish Community Center of San Francisco, 3200 California Street, San Francisco, San Francisco County, CA

  9. Prolonged swimming performance of northern squawfish

    USGS Publications Warehouse

    Mesa, Matthew G.; Olson, Todd M.

    1993-01-01

    We determined the prolonged swimming performance of two size-classes of northern squawfish Ptychocheilus oregonensis at 12 and 18°C. The percentage of fish fatigued was positively related to water velocity and best described by an exponential model. At 12°C, the velocity at which 50% of the fish fatigued (FV50) was estimated to be 2.91 fork lengths per second (FL/s; 100 cm/s) for medium-sized fish (30–39 cm) and 2.45 FL/s (104 cm/s) for large fish (40–49 cm). At 18°C, estimated FV50 was 3.12 FL/s (107 cm/s) for medium fish and 2.65 FL/s (112 cm/s) for large fish. Rate of change in percent fatigue was affected by fish size and water temperature. Large fish fatigued at a higher rate than medium-sized fish; all fish fatigued faster at 12 than at 18°C. The mean times to fatigue at velocities of 102–115 cm/s ranged from 14 to 28 min and were not affected by fish size or water temperature. Our results indicate that water velocities from 100 to 130 cm/s may exclude or reduce predation by northern squawfish around juvenile salmonid bypass outfalls at Columbia River dams, at least during certain times of the year. We recommend that construction or modification of juvenile salmonid bypass facilities place the outfall in an area of high water velocity and distant from eddies, submerged cover, and littoral areas.

  10. Prolonged swimming performance of northern squawfish

    SciTech Connect

    Mesa, M.G.; Olson, T.M. )

    1993-11-01

    The authors determined the prolonged swimming performance of two size-classes of northern squawfish Ptychocheilus oregonensis at 12 and 18[degrees]C. The percentage of fish fatigued was positively related to water velocity and best described by an exponential model. At 12[degrees]C, the velocity at which 50% of the fish fatigued (FV50) was estimated to be 2.91 fork lengths per second (FL/s; 100 cm/s) for medium-sized fish (30-39 cm) and 2.45 FL/s (104 cm/s) for large fish (40-49 cm). At 18[degrees]C, estimated FV50 was 3.12 FL/s (107 cm/s) for medium fish and 2.65 FL/s (112 cm/s) for large fish. Rate of change in percent fatigue was affected by fish size and water temperature. Large fish fatigued at a higher rate than medium-sized fish; all fish fatigued faster at 12 than at 18[degrees]C. The mean times to fatigue at velocities of 102-115 cm/s ranged from 14 to 28 min and were not affected by fish size or water temperature. The results indicate that water velocities from 100 to 130 cm/s may exclude or reduce predation by northern squawfish around juvenile salmonid bypass outfalls at Columbia River dams, at least during certain times of the year. The authors recommend that construction or modification of juvenile salmonid bypass facilities place the outfall in an area of high water velocity and distant from eddies, submerged cover, and littoral areas. 35 refs., 1 fig., 2 tabs.

  11. 2008 Swimming Season Fact Sheets

    EPA Pesticide Factsheets

    To help beachgoers make informed decisions about swimming at U.S. beaches, EPA annually publishes state-by-state data about beach closings and advisories for the previous year's swimming season. These fact sheets summarize that information by state.

  12. 2007 Swimming Season Fact Sheets

    EPA Pesticide Factsheets

    To help beachgoers make informed decisions about swimming at U.S. beaches, EPA annually publishes state-by-state data about beach closings and advisories for the previous year's swimming season. These fact sheets summarize that information by state.

  13. 2009 Swimming Season Fact Sheets

    EPA Pesticide Factsheets

    To help beachgoers make informed decisions about swimming at U.S. beaches, EPA annually publishes state-by-state data about beach closings and advisories for the previous year's swimming season. These fact sheets summarize that information by state.

  14. 2006 Swimming Season Fact Sheets

    EPA Pesticide Factsheets

    To help beachgoers make informed decisions about swimming at U.S. beaches, EPA annually publishes state-by-state data about beach closings and advisories for the previous year's swimming season. These fact sheets summarize that information by state.

  15. 2010 Swimming Season Fact Sheets

    EPA Pesticide Factsheets

    To help beachgoers make informed decisions about swimming at U.S. beaches, EPA annually publishes state-by-state data about beach closings and advisories for the previous year's swimming season. These fact sheets summarize that information by state.

  16. Simulations of optimized anguilliform swimming.

    PubMed

    Kern, Stefan; Koumoutsakos, Petros

    2006-12-01

    The hydrodynamics of anguilliform swimming motions was investigated using three-dimensional simulations of the fluid flow past a self-propelled body. The motion of the body is not specified a priori, but is instead obtained through an evolutionary algorithm used to optimize the swimming efficiency and the burst swimming speed. The results of the present simulations support the hypothesis that anguilliform swimmers modify their kinematics according to different objectives and provide a quantitative analysis of the swimming motion and the forces experienced by the body. The kinematics of burst swimming is characterized by the large amplitude of the tail undulations while the anterior part of the body remains straight. In contrast, during efficient swimming behavior significant lateral undulation occurs along the entire length of the body. In turn, during burst swimming, the majority of the thrust is generated at the tail, whereas in the efficient swimming mode, in addition to the tail, the middle of the body contributes significantly to the thrust. The burst swimming velocity is 42% higher and the propulsive efficiency is 15% lower than the respective values during efficient swimming. The wake, for both swimming modes, consists largely of a double row of vortex rings with an axis aligned with the swimming direction. The vortex rings are responsible for producing lateral jets of fluid, which has been documented in prior experimental studies. We note that the primary wake vortices are qualitatively similar in both swimming modes except that the wake vortex rings are stronger and relatively more elongated in the fast swimming mode. The present results provide quantitative information of three-dimensional fluid-body interactions that may complement related experimental studies. In addition they enable a detailed quantitative analysis, which may be difficult to obtain experimentally, of the different swimming modes linking the kinematics of the motion with the forces

  17. Swimming Pools for Primary Schools.

    ERIC Educational Resources Information Center

    Klein, Jo

    This seven-chapter report on swimming in primary schools deals with the policies of local British education authorities and institutes for the physically handicapped toward promoting swimming. Interspersed throughout are comments from teachers and children. "Swimming and Education" comments on the benefits of primary school swimming…

  18. Observations on side-swimming rainbow trout in water recirculation aquaculture systems.

    PubMed

    Good, Christopher; Davidson, John; Kinman, Christin; Kenney, P Brett; Bæverfjord, Grete; Summerfelt, Steven

    2014-12-01

    During a controlled 6-month study using six replicated water recirculation aquaculture systems (WRASs), it was observed that Rainbow Trout Oncorhynchus mykiss in all WRASs exhibited a higher-than-normal prevalence of side swimming (i.e., controlled, forward swimming but with misaligned orientation such that the fish's sagittal axis is approximately parallel to the horizontal plane). To further our understanding of this abnormality, a substudy was conducted wherein side swimmers and normally swimming fish were selectively sampled from each WRAS and growth performance (length, weight), processing attributes (fillet yield, visceral index, ventrum [i.e., thickness of the ventral "belly flap"] index), blood gas and chemistry parameters, and swim bladder morphology and positioning were compared. Side swimmers were found to be significantly smaller in length and weight and had less fillet yield but higher ventrum indices. Whole-blood analyses demonstrated that, among other things, side swimmers had significantly lower whole-blood pH and higher Pco2. Side swimmers typically exhibited swim bladder malformations, although the positive predictive value of this subjective assessment was only 73%. Overall, this study found several anatomical and physiological differences between side-swimming and normally swimming Rainbow Trout. Given the reduced weight and fillet yield of market-age side swimmers, producers would benefit from additional research to reduce side-swimming prevalence in their fish stocks.

  19. Just Keep Swimming: Neuroendocrine, Metabolic, and Behavioral Changes After a Forced Swimming Test in Zebrafish.

    PubMed

    da Rosa, João Gabriel Santos; Barcellos, Heloísa Helena de Alcântara; Idalencio, Renan; Marqueze, Alessandra; Fagundes, Michele; Rossini, Mainara; Variani, Cristiane; Balbinoti, Francine; Tietböhl, Tássia Michele Huff; Rosemberg, Denis Broock; Barcellos, Leonardo José Gil

    2017-02-01

    In this study, we show that an adaptation of the spinning test can be used as a model to study the exercise-exhaustion-recovery paradigm in fish. This forced swimming test promotes a wide range of changes in the hypothalamus-pituitary-interrenal axis functioning, intermediary metabolism, as well in fish behavior at both exercise and recovery periods. Our results pointed that this adapted spinning test can be considered a valuable tool for evaluating drugs and contaminant effects on exercised fish. This can be a suitable protocol both to environmental-to evaluate contaminants that act in fish energy mobilization and recovery after stressors-and translational perspectives-effects of drugs on exercised or stressed humans.

  20. Relationships between metabolic rate, muscle electromyograms, and swim performance of adult chinook salmon

    SciTech Connect

    Geist, David R. ); Brown, Richard S. ); Cullinan, Valerie I. ); Mesa, Matthew G.; VanderKooi, S P.; McKinstry, Craig A. )

    2003-10-01

    We measured oxygen consumption rates of adult spring Chinook salmon and compared these values to other species of Pacific salmon. Our results indicated that adult salmon achieve their maximum level of oxygen consumption at about their upper critical swim speed. It is also at this speed that the majority of the energy supplied to the swimming fish switches from red muscle (powered by aerobic metabolism) to white muscle (powered by anaerobic metabolism). Determining the swimming performance of adult salmon will assist managers in developing fishways and other means to safely pass fish over hydroelectric dams and other man-made structures.

  1. Effects of skeletal deformities on swimming performance and recovery from exhaustive exercise in triploid Atlantic salmon.

    PubMed

    Powell, Mark D; Jones, Matthew A; Lijalad, Maite

    2009-05-27

    The occurrence of spinal deformity in aquaculture can be considerable, and a high rate of deformity has been suggested in triploid smolts in Tasmania. However, the physiological performance of fish with skeletal deformities has not been addressed. The swimming performance and oxygen consumption of triploid Atlantic salmon smolts with either a vertebral fusion (platyspondyly) or multifocal scoliosis were compared to normal (non-deformed) triploid smolts. Fish with vertebral fusion attained swim speeds similar to normal fish, whereas scoliotic fish were unable to attain comparable swim speeds. Routine and maximum oxygen consumption was higher for deformed fish compared with normal fish, translating into apparent increased routine metabolic scope in vertebral fusion fish, and equivocal scope in scoliotic fish compared with normal controls. Deformed fish developed a lower excess post-exercise oxygen consumption compared to non-deformed fish, suggesting they are either incapable of sustained anaerobic activity or possess an increased recovery capacity. These data suggest that skeletal deformity has differential effects on swimming performance depending upon the type of deformity but imposes a significant metabolic cost on salmon smolts.

  2. Red Cross Swimming Update.

    ERIC Educational Resources Information Center

    Vlasich, Cynthia

    1989-01-01

    Six new aquatic courses, developed by the Red Cross, are described. They are: Infant and Preschool Aquatics, Longfellow's Whale Tales (classroom water safety lessons for K-Six), Basic Water Safety, Emergency Water Safety, Lifeguard Training, and Safety Training for Swim Coaches. (IAH)

  3. Elastic swimming II: Experiments

    NASA Astrophysics Data System (ADS)

    Yu, Tony; Lauga, Eric; Hosoi, Anette

    2006-03-01

    We consider the problem of swimming at low Reynolds number by oscillating an elastic filament in a viscous liquid, as investigated by Wiggins and Goldstein (1998, Phys Rev Lett). In this second part of the study, we present results of a series of experiments characterizing the performance of the propulsive mechanism.

  4. Red Cross Swimming Update.

    ERIC Educational Resources Information Center

    Vlasich, Cynthia

    1989-01-01

    Six new aquatic courses, developed by the Red Cross, are described. They are: Infant and Preschool Aquatics, Longfellow's Whale Tales (classroom water safety lessons for K-Six), Basic Water Safety, Emergency Water Safety, Lifeguard Training, and Safety Training for Swim Coaches. (IAH)

  5. Changes in the swimming activity and the glutathione S-transferase activity of Jenynsia multidentata fed with microcystin-RR.

    PubMed

    Cazenave, Jimena; Nores, María L; Miceli, Martín; Díaz, María P; Wunderlin, Daniel A; Bistoni, María A

    2008-02-01

    We report the effects of sublethal doses of microcystin-RR (MC-RR) on the swimming activity of Jenynsia multidentata as well as the simultaneous response of its detoxication system by measuring glutathion S-transferase (GST) activities in the liver and brain of fish. MC-RR was applied on the food pellets at doses of 0.01, 0.1 and 1 microg g(-1). Swimming activity was recorded 10 min each hour over 24h by using a computer-based image processing system, which facilitates quantification of two measures of fish swimming behaviour (average velocity, movement percentage). Results show that low levels of cyanotoxin increased the swimming activity, while the highest dose used produced significant changes with respect to control group only since approximately 20 h of exposure, when the swimming activity was decreased. On the other hand, GST activity was significantly increased only in the liver and brain of fish fed with the highest MC-RR dose. Both results suggest that fish are reacting to the stress caused by low doses of MC-RR by increasing their swimming activity, raising further questions on the probable neurotoxicity of MCs, and presenting the behavioural change as a good biomarker of early toxic stress. On the other hand, fish reduced their swimming speed at the highest MC-RR dose, when the detoxication activity began, which can be hypothesized to be a reallocation of their energy, favouring detoxication over swimming activity.

  6. Impaired swim bladder inflation in early-life stage fathead ...

    EPA Pesticide Factsheets

    The present study investigated whether inhibition of deiodinase, the enzyme which converts thyroxine (T4) to the more biologically-active form, 3,5,3'-triiodothyronine (T3), would impact inflation of the posterior and/or anterior chamber of the swim bladder, processes previously demonstrated to be thyroid-hormone regulated. Two experiments were conducted using a model deiodinase inhibitor, iopanoic acid (IOP). In the first study, fathead minnow (Pimephales promelas) embryos were exposed to 0.6, 1.9, or 6.0 mg IOP/L or control water in a flow-through system until reaching 6 days post-fertilization (dpf) at which time posterior swim bladder inflation was assessed. To examine effects on anterior swim bladder inflation, a second study was conducted with 6 dpf larvae exposed to the same IOP concentrations until reaching 21 dpf. Fish from both studies were sampled for T4/T3 measurements, gene transcription analyses, and thyroid histopathology. In the embryo study, incidence and length of inflated posterior swim bladders were significantly reduced in the 6.0 mg/L treatment at 6 dpf. Incidence of inflation and length of anterior swim bladder in larval fish were significantly reduced in all IOP treatments at 14 dpf, but inflation recovered by 18 dpf. Throughout the larval study, whole body T4 concentrations were significantly increased and T3 concentrations were significantly decreased in all IOP treatments. Consistent with hypothesized compensatory responses, sig

  7. Impaired swim bladder inflation in early-life stage fathead ...

    EPA Pesticide Factsheets

    The present study investigated whether inhibition of deiodinase, the enzyme which converts thyroxine (T4) to the more biologically-active form, 3,5,3'-triiodothyronine (T3), would impact inflation of the posterior and/or anterior chamber of the swim bladder, processes previously demonstrated to be thyroid-hormone regulated. Two experiments were conducted using a model deiodinase inhibitor, iopanoic acid (IOP). In the first study, fathead minnow (Pimephales promelas) embryos were exposed to 0.6, 1.9, or 6.0 mg IOP/L or control water in a flow-through system until reaching 6 days post-fertilization (dpf) at which time posterior swim bladder inflation was assessed. To examine effects on anterior swim bladder inflation, a second study was conducted with 6 dpf larvae exposed to the same IOP concentrations until reaching 21 dpf. Fish from both studies were sampled for T4/T3 measurements, gene transcription analyses, and thyroid histopathology. In the embryo study, incidence and length of inflated posterior swim bladders were significantly reduced in the 6.0 mg/L treatment at 6 dpf. Incidence of inflation and length of anterior swim bladder in larval fish were significantly reduced in all IOP treatments at 14 dpf, but inflation recovered by 18 dpf. Throughout the larval study, whole body T4 concentrations were significantly increased and T3 concentrations were significantly decreased in all IOP treatments. Consistent with hypothesized compensatory responses, sig

  8. Use of pneumocystoplasty for overinflation of the swim bladder in a goldfish.

    PubMed

    Britt, Tara; Weisse, Chick; Weber, E Scott; Matzkin, Zach; Klide, Alan

    2002-09-01

    A Ryukin goldfish was evaluated because of a 6-month history of progressive abdominal distention and positive buoyancy. Overinflation of the swim bladder was diagnosed, and the fish was anesthetized with tricaine methanesulfonate. Archimedes' principle was used to determine the volume of swim bladder that was removed surgically. The caudal swim bladder was exteriorized through an abdominal incision and 2 surgical clips were placed across it to limit its size. After surgery, the fish remained in a state of negative buoyancy in sternal and lateral recumbency on the bottom of the tank. Sutures were removed 15 days after surgery, but the fish died 24 days after surgery. A full necropsy could not be performed because of autolysis of the tissues, but the surgical clips and the swim bladder appeared unremarkable. Pneumocystoplasty may be a viable treatment for this condition.

  9. Influence of externally attached transmitters on the swimming performance of juvenile white sturgeon

    USGS Publications Warehouse

    Counihan, T.D.; Frost, C.N.

    1999-01-01

    We measured the critical swimming speed of juvenile white sturgeons Acipenser transmontanus equipped with externally attached dummy ultrasonic transmitters and of untagged control fish in the laboratory. White sturgeons ranging from 31.9 to 37.0 cm fork length were subjected to one of three treatments: control (handled but not tagged), tag attached below the dorsal fin, and tag attached with the anterior insertion point between the fourth and fifth dorsal scutes. Although transmitters were of recommended weight, we found that the swimming performance of tagged white sturgeons was significantly less than that of untagged control fish. Swimming performance of tagged fish was not differentially affected by tag location. Our results suggest that data from ultrasonic telemetry studies of externally tagged juvenile white sturgeons should be interpreted with caution due to the reduced swimming performance caused by external transmitters.

  10. Influence of externally attached trasmitters on the swimming performance of juvenile white sturgeon

    USGS Publications Warehouse

    Counihan, T.D.; Frost, C.N.

    1999-01-01

    We measured the critical swimming speed of juvenile white sturgeons Acipenser transmontanus equipped with externally attached dummy ultrasonic transmitters and of untagged control fish in the laboratory. White sturgeons ranging from 31.9 to 37.0 cm fork length were subjected to one of three treatments: Control (handled but not tagged), tag attached below the dorsal fin, and tag attached with the anterior insertion point between the fourth and fifth dorsal scutes. Although transmitters were of recommended weight, we found that the swimming performance of tagged white sturgeons was significantly less than that of untagged control fish. Swimming performance of tagged fish was not differentially affected by tag location. Our results suggest that data from ultrasonic telemetry studies of externally tagged juvenile white sturgeons should be interpreted with caution due to the reduced swimming performance caused by external transmitters.

  11. Similarities and Differences for Swimming in Larval and Adult Lampreys.

    PubMed

    McClellan, Andrew D; Pale, Timothée; Messina, J Alex; Buso, Scott; Shebib, Ahmad

    2016-01-01

    The spinal locomotor networks controlling swimming behavior in larval and adult lampreys may have some important differences. As an initial step in comparing the locomotor systems in lampreys, in larval animals the relative timing of locomotor movements and muscle burst activity were determined and compared to those previously published for adults. In addition, the kinematics for free swimming in larval and adult lampreys was compared in detail for the first time. First, for swimming in larval animals, the neuromechanical phase lag between the onsets or terminations of muscle burst activity and maximum concave curvature of the body increased with increasing distance along the body, similar to that previously shown in adults. Second, in larval lampreys, but not adults, absolute swimming speed (U; mm s(-1)) increased with animal length (L). In contrast, normalized swimming speed (U'; body lengths [bl] s(-1)) did not increase with L in larval or adult animals. In both larval and adult lampreys, U' and normalized wave speed (V') increased with increasing tail-beat frequency. Wavelength and mechanical phase lag did not vary significantly with tail-beat frequency but were significantly different in larval and adult animals. Swimming in larval animals was characterized by a smaller U/V ratio, Froude efficiency, and Strouhal number than in adults, suggesting less efficient swimming for larval animals. In addition, during swimming in larval lampreys, normalized lateral head movements were larger and normalized lateral tail movements were smaller than for adults. Finally, larval animals had proportionally smaller lateral surface areas of the caudal body and fin areas than adults. These differences are well suited for larval sea lampreys that spend most of the time buried in mud/sand, in which swimming efficiency is not critical, compared to adults that would experience significant selection pressure to evolve higher-efficiency swimming to catch up to and attach to fish for

  12. Warm Water and Cool Nests Are Best. How Global Warming Might Influence Hatchling Green Turtle Swimming Performance

    PubMed Central

    Booth, David T.; Evans, Andrew

    2011-01-01

    For sea turtles nesting on beaches surrounded by coral reefs, the most important element of hatchling recruitment is escaping predation by fish as they swim across the fringing reef, and as a consequence hatchlings that minimize their exposure to fish predation by minimizing the time spent crossing the fringing reef have a greater chance of surviving the reef crossing. One way to decrease the time required to cross the fringing reef is to maximize swimming speed. We found that both water temperature and nest temperature influence swimming performance of hatchling green turtles, but in opposite directions. Warm water increases swimming ability, with hatchling turtles swimming in warm water having a faster stroke rate, while an increase in nest temperature decreases swimming ability with hatchlings from warm nests producing less thrust per stroke. PMID:21826236

  13. Warm water and cool nests are best. How global warming might influence hatchling green turtle swimming performance.

    PubMed

    Booth, David T; Evans, Andrew

    2011-01-01

    For sea turtles nesting on beaches surrounded by coral reefs, the most important element of hatchling recruitment is escaping predation by fish as they swim across the fringing reef, and as a consequence hatchlings that minimize their exposure to fish predation by minimizing the time spent crossing the fringing reef have a greater chance of surviving the reef crossing. One way to decrease the time required to cross the fringing reef is to maximize swimming speed. We found that both water temperature and nest temperature influence swimming performance of hatchling green turtles, but in opposite directions. Warm water increases swimming ability, with hatchling turtles swimming in warm water having a faster stroke rate, while an increase in nest temperature decreases swimming ability with hatchlings from warm nests producing less thrust per stroke.

  14. Unsteady bio-fluid dynamics in flying and swimming

    NASA Astrophysics Data System (ADS)

    Liu, Hao; Kolomenskiy, Dmitry; Nakata, Toshiyuki; Li, Gen

    2017-08-01

    Flying and swimming in nature present sophisticated and exciting ventures in biomimetics, which seeks sustainable solutions and solves practical problems by emulating nature's time-tested patterns, functions, and strategies. Bio-fluids in insect and bird flight, as well as in fish swimming are highly dynamic and unsteady; however, they have been studied mostly with a focus on the phenomena associated with a body or wings moving in a steady flow. Characterized by unsteady wing flapping and body undulation, fluid-structure interactions, flexible wings and bodies, turbulent environments, and complex maneuver, bio-fluid dynamics normally have challenges associated with low Reynolds number regime and high unsteadiness in modeling and analysis of flow physics. In this article, we review and highlight recent advances in unsteady bio-fluid dynamics in terms of leading-edge vortices, passive mechanisms in flexible wings and hinges, flapping flight in unsteady environments, and micro-structured aerodynamics in flapping flight, as well as undulatory swimming, flapping-fin hydrodynamics, body-fin interaction, C-start and maneuvering, swimming in turbulence, collective swimming, and micro-structured hydrodynamics in swimming. We further give a perspective outlook on future challenges and tasks of several key issues of the field.

  15. Unsteady bio-fluid dynamics in flying and swimming

    NASA Astrophysics Data System (ADS)

    Liu, Hao; Kolomenskiy, Dmitry; Nakata, Toshiyuki; Li, Gen

    2017-06-01

    Flying and swimming in nature present sophisticated and exciting ventures in biomimetics, which seeks sustainable solutions and solves practical problems by emulating nature's time-tested patterns, functions, and strategies. Bio-fluids in insect and bird flight, as well as in fish swimming are highly dynamic and unsteady; however, they have been studied mostly with a focus on the phenomena associated with a body or wings moving in a steady flow. Characterized by unsteady wing flapping and body undulation, fluid-structure interactions, flexible wings and bodies, turbulent environments, and complex maneuver, bio-fluid dynamics normally have challenges associated with low Reynolds number regime and high unsteadiness in modeling and analysis of flow physics. In this article, we review and highlight recent advances in unsteady bio-fluid dynamics in terms of leading-edge vortices, passive mechanisms in flexible wings and hinges, flapping flight in unsteady environments, and micro-structured aerodynamics in flapping flight, as well as undulatory swimming, flapping-fin hydrodynamics, body-fin interaction, C-start and maneuvering, swimming in turbulence, collective swimming, and micro-structured hydrodynamics in swimming. We further give a perspective outlook on future challenges and tasks of several key issues of the field.

  16. Relationships between metabolic rate, muscle electromyograms and swim performance of adult chinook salmon

    USGS Publications Warehouse

    Geist, D.R.; Brown, R.S.; Cullinan, V.I.; Mesa, M.G.; VanderKooi, S.P.; McKinstry, C.A.

    2003-01-01

    Oxygen consumption rates of adult spring chinook salmon Oncorhynchus tshawytscha increased with swim speed and, depending on temperature and fish mass, ranged from 609 mg O2 h-1 at 30 cm s-1 (c. 0.5 BLs-1) to 3347 mg O2 h-1 at 170 cm s -1 (c. 2.3 BLs-1). Corrected for fish mass, these values ranged from 122 to 670 mg O2 kg-1 h-1, and were similar to other Oncorhynchus species. At all temperatures (8, 12.5 and 17??C), maximum oxygen consumption values levelled off and slightly declined with increasing swim speed >170 cm s-1, and a third-order polynomial regression model fitted the data best. The upper critical swim speed (Ucrit) of fish tested at two laboratories averaged 155 cm s -1 (2.1 BLs-1), but Ucrit of fish tested at the Pacific Northwest National Laboratory were significantly higher (mean 165 cm s-1) than those from fish tested at the Columbia River Research Laboratory (mean 140 cm s-1). Swim trials using fish that had electromyogram (EMG) transmitters implanted in them suggested that at a swim speed of c. 135 cm s-1, red muscle EMG pulse rates slowed and white muscle EMG pulse rates increased. Although there was significant variation between individual fish, this swim speed was c. 80% of the Ucrit for the fish used in the EMG trials (mean Ucrit 168.2 cm s-1). Bioenergetic modelling of the upstream migration of adult chinook salmon should consider incorporating an anaerobic fraction of the energy budget when swim speeds are ???80% of the Ucrit. ?? 2003 The Fisheries Society of the British Isles.

  17. Fish locomotion: recent advances and new directions.

    PubMed

    Lauder, George V

    2015-01-01

    Research on fish locomotion has expanded greatly in recent years as new approaches have been brought to bear on a classical field of study. Detailed analyses of patterns of body and fin motion and the effects of these movements on water flow patterns have helped scientists understand the causes and effects of hydrodynamic patterns produced by swimming fish. Recent developments include the study of the center-of-mass motion of swimming fish and the use of volumetric imaging systems that allow three-dimensional instantaneous snapshots of wake flow patterns. The large numbers of swimming fish in the oceans and the vorticity present in fin and body wakes support the hypothesis that fish contribute significantly to the mixing of ocean waters. New developments in fish robotics have enhanced understanding of the physical principles underlying aquatic propulsion and allowed intriguing biological features, such as the structure of shark skin, to be studied in detail.

  18. Fish Locomotion: Recent Advances and New Directions

    NASA Astrophysics Data System (ADS)

    Lauder, George V.

    2015-01-01

    Research on fish locomotion has expanded greatly in recent years as new approaches have been brought to bear on a classical field of study. Detailed analyses of patterns of body and fin motion and the effects of these movements on water flow patterns have helped scientists understand the causes and effects of hydrodynamic patterns produced by swimming fish. Recent developments include the study of the center-of-mass motion of swimming fish and the use of volumetric imaging systems that allow three-dimensional instantaneous snapshots of wake flow patterns. The large numbers of swimming fish in the oceans and the vorticity present in fin and body wakes support the hypothesis that fish contribute significantly to the mixing of ocean waters. New developments in fish robotics have enhanced understanding of the physical principles underlying aquatic propulsion and allowed intriguing biological features, such as the structure of shark skin, to be studied in detail.

  19. The hydrodynamics of eel swimming: I. Wake structure.

    PubMed

    Tytell, Eric D; Lauder, George V

    2004-05-01

    Eels undulate a larger portion of their bodies while swimming than many other fishes, but the hydrodynamic consequences of this swimming mode are poorly understood. In this study, we examine in detail the hydrodynamics of American eels (Anguilla rostrata) swimming steadily at 1.4 L s(-1) and compare them with previous results from other fishes. We performed high-resolution particle image velocimetry (PIV) to quantify the wake structure, measure the swimming efficiency, and force and power output. The wake consists of jets of fluid that point almost directly laterally, separated by an unstable shear layer that rolls up into two or more vortices over time. Previously, the wake of swimming eels was hypothesized to consist of unlinked vortex rings, resulting from a phase offset between vorticity distributed along the body and vorticity shed at the tail. Our high-resolution flow data suggest that the body anterior to the tail tip produces relatively low vorticity, and instead the wake structure results from the instability of the shear layers separating the lateral jets, reflecting pulses of high vorticity shed at the tail tip. We compare the wake structure to large-amplitude elongated body theory and to a previous computational fluid dynamic model and note several discrepancies between the models and the measured values. The wake of steadily swimming eels differs substantially in structure from the wake of previously studied carangiform fishes in that it lacks any significant downstream flow, previously interpreted as signifying thrust. We infer that the lack of downstream flow results from a spatial and temporal balance of momentum removal (drag) and thrust generated along the body, due to the relatively uniform shape of eels. Carangiform swimmers typically have a narrow caudal peduncle, which probably allows them to separate thrust from drag both spatially and temporally. Eels seem to lack this separation, which may explain why they produce a wake with little

  20. Sprint swimming performance of wild bull trout (Salvelinus confluentus)

    USGS Publications Warehouse

    Mesa, M.G.; Phelps, J.; Weiland, L.K.

    2008-01-01

    We conducted laboratory experiments to determine the sprint swimming performance of wild juvenile and adult bull trout Salvelinus confluentus. Sprint swimming speeds were estimated using high-speed digital video analysis. Thirty two bull trout were tested in sizes ranging from about 10 to 31 cm. Of these, 14 fish showed at least one motivated, vigorous sprint. When plotted as a function of time, velocity of fish increased rapidly with the relation linear or slightly curvilinear. Their maximum velocity, or Vmax, ranged from 1.3 to 2.3 m/s, was usually achieved within 0.8 to 1.0 s, and was independent of fish size. Distances covered during these sprints ranged from 1.4 to 2.4 m. Our estimates of the sprint swimming performance are the first reported for this species and may be useful for producing or modifying fish passage structures that allow safe and effective passage of fish without overly exhausting them. ?? 2008 by the Northwest Scientific Association. All rights reserved.

  1. Hydrodynamics of Fishlike Swimming: Effects of swimming kinematics and Reynolds number

    NASA Astrophysics Data System (ADS)

    Gilmanov, Anvar; Posada, Nicolas; Sotiropoulos, Fotis

    2003-11-01

    We carry out a series of numerical simulations to investigate the effects of swimming kinematics and Reynolds number on the flow past a three-dimensional fishlike body undergoing undulatory motion. The simulated body shape is that of a real mackerel fish. The mackerel was frozen and subsequently sliced in several thin fillets whose dimensions were carefully measured and used to construct the fishlike body shape used in the simulations. The flow induced by the undulating body is simulated by solving the 3D, unsteady, incompressible Navier-Stokes equations with the second-order accurate, hybrid Cartesian/Immersed Boundary formulation of Gilmanov and Sotiropoulos (J. Comp. Physics, under review, 2003). We consider in-line swimming at constant speed and carry out simulations for various types of swimming kinematics, varying the tailbeat amplitude, frequency, and Reynolds number (300fish wake and the role of these vortices on drag reduction, thrust procuction, and propulsive efficiency.

  2. Effect of morphological fin curl on the swimming performance and station-holding ability of juvenile shovelnose sturgeon

    USGS Publications Warehouse

    Deslauriers, David; Johnston, Ryan; Chipps, Steven R.

    2016-01-01

    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 < 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.

  3. Why fishes have a fish shape

    NASA Astrophysics Data System (ADS)

    Eloy, Christophe; Schouveiler, Lionel

    2010-11-01

    The relation between form and function for elongated swimmers is revisited by solving a multi-objective optimization problem. We consider elongated fishes of varying elliptic cross-section whose motion is prescribed by a time-periodic curvature. The two semi-axes of the cross-section, the curvature amplitude and phase are assumed to vary continuously along the fish length. Hydrodynamic forces acting on such fishes are modeled in the elongated-body limit by considering both reactive and resistive forces. Applying Newton's second law, the heave and pitch amplitude and phase, as well as the swimming velocity can be found. The total power needed can also be calculated yielding the swimming efficiency. The multi-objective optimization consists in finding the fish shape and associated motion which corresponds to maximum efficiency, maximum velocity or any trade-off between the two. This optimization problem is solved using a genetic algorithm whose principle is to start with an initial random population and to evolve it by mutation and selection. We find that the most efficient shape resembles existing fishes and arguments are given to explain the relation between this particular fish form and performance.

  4. A kinematic and dynamic comparison of surface and underwater displacement in high level monofin swimming.

    PubMed

    Nicolas, Guillaume; Bideau, Benoit

    2009-08-01

    Fin swimming performance can be divided into underwater and surface water races. World records are about 10% faster for underwater swimming vs. surface swimming, but little is known about the advantage of underwater swimming for monofin swimming. Some authors reported that the air-water interface influences the kinematics and leads to a narrow vertical amplitude of the fin. On the one hand, surface swimming is expected to affect drag parameters (cross-sectional area (S) and active drag (AD)) when compared to underwater swimming. On the other hand, the surface swimming technique may also affect efficiency (eta(F)). The aim of this study is therefore to evaluate and compare drag parameters and efficiency during underwater and surface swimming. To this end, 12 international level monofin swimmers were measured during both underwater and surface swimming. Kinematic parameters (both dimensional and non-dimensional), eta(F) (calculated according to the Elongated-Body Theory), and AD (computed with Velocity Perturbation Method) were calculated for an underwater and a surface fin swimming trial, performed at maximal speed. As expected, results showed significantly lower velocities during surface swimming vs. underwater V(1,under) =2.5ms(-1) vs. V(1,surf) =2.36ms(-1), p<.01). Velocities during underwater and surface swimming were strongly correlated (r=.97, p<.01). Underwater swimming was also associated with higher vertical amplitudes of the fin compared to surface swimming (V(under) =0.55mvs. V(surf) )=0.46m, p<.01). Length-specific amplitudes (A(under)/L(b)) were in the order of 20% during underwater swimming as for undulating fish, and significantly higher than during surface swimming (A(surf)/L(b)=17%, p<.01). Efficiency for surface swimming was about 6% lower than for underwater swimming (eta(F,under) =0.79 vs. eta(F,surf) =0.74, p<.01). This decrease could be associated with an increase in swimming frequency for surface swimming (f (surf)=2.15Hz vs. f (under)=2.08Hz

  5. Mechanics of Mammalian Swimming

    NASA Astrophysics Data System (ADS)

    Wei, Timothy; Legac, Paul; Fish, Frank; Williams, Terrie; Mark, Russell; Hutchison, Sean

    2008-03-01

    Propulsion of large mammals (i.e. dolphins and humans) has been of great interest for both technological and athletic reasons. The foundational question is how fast can a mammal swim? Digital Particle Image Velocimetry (DPIV) has been modified to be safely used on swimmers and dolphins. Experiments of dolphins performing various swimming behaviors were performed at the Long Marine Laboratory, University of California, Santa Cruz. Vortices generated by the dolphins' tail motions were used to estimate thrust production. Also, a two-dimensional dynamic force balance was constructed to study and improve the mechanics of elite swimmers. Paired with an underwater video camera, the forces seen could be directly related to the motion of the swimmer. These force measurements could be correlated to time resolved DPIV measurements of flow around the swimmers. Measurements made with swimmers, Megan Jendrick (2000 Olympic gold medalist) and Ariana Kukors (4x US National Champion), as well as data from trials with two dolphins will be presented.

  6. Drafting distance in swimming.

    PubMed

    Chatard, Jean-Claude; Wilson, Barry

    2003-07-01

    This study investigates the effect of the distance separating the lead and draft swimmers on the metabolic and hydrodynamic responses of the draft swimmer. A nondrafting swim of 4 min at 95% of the best 1500-m pace for 11 swimmers was compared with swimming in a drafting position at four different distances directly behind another swimmer (0, 50, 100, and 150 cm). Swimming performance was assessed by stroke rate and stroke length; the metabolic response by oxygen uptake, heart rate, and blood lactate; and the rating of perceived exertion by the Borg scale. Passive drag was assessed at these drafting distances by passive towing. Then, passive drag was measured in six swimmers towed in six lateral drafting positions, with swimmers separated by approximately 40 cm, and then measured in two positions at the rear of the lead swimmer with a reduced lateral distance between swimmers of 50 and 0 cm. Oxygen uptake, heart rate, blood lactate, rating of perceived exertion, and stroke rate were significantly reduced and stroke length was significantly increased in all drafting positions compared with the nondrafting position. For drag, the most advantageous drafting distances were 0 and 50 cm back from the toes of the lead swimmer. Drag was reduced by 21% and 20%, respectively. In lateral drafting, drag was significantly reduced by 6% and 7%, respectively, at 50 and 100 cm back from the hands of the lead swimmer. Swimming behind another swimmer at a distance between 0 and 50 cm back from the toes was the most advantageous, whereas in lateral drafting the optimal distance was 50-100 cm back from the hands of the lead swimmer.

  7. Going for a Swim

    ERIC Educational Resources Information Center

    Covington, Savannah

    2016-01-01

    Is anything more refreshing than going for a nice, long swim? The math scenarios presented in this article will take the reader back to hot summer days and remind the reader what a cool dip in the water feels like. Solving these problems is enjoyable and encourages the solver to think of the many ways that math is all around--even in the middle of…

  8. Going for a Swim

    ERIC Educational Resources Information Center

    Covington, Savannah

    2016-01-01

    Is anything more refreshing than going for a nice, long swim? The math scenarios presented in this article will take the reader back to hot summer days and remind the reader what a cool dip in the water feels like. Solving these problems is enjoyable and encourages the solver to think of the many ways that math is all around--even in the middle of…

  9. Swimming in external fields

    NASA Astrophysics Data System (ADS)

    Stark, Holger

    2016-11-01

    Microswimmers move autonomously but are subject to external fields, which influence their swimming path and their collective dynamics. With three concrete examples we illustrate swimming in external fields and explain the methodology to treat it. First, an active Brownian particle shows a conventional sedimentation profile in a gravitational field but with increased sedimentation length and some polar order along the vertical. Bottom-heavy swimmers are able to invert the sedimentation profile. Second, active Brownian particles interacting by hydrodynamic flow fields in a three-dimensional harmonic trap can spontaneously break the isotropic symmetry. They develop polar order, which one can describe by mean-field theory reminiscent to Weiss theory of ferromagnetism, and thereby pump fluid. Third, a single microswimmer shows interesting non-linear dynamics in Poiseuille flow including swinging and tumbling trajectories. For pushers, hydrodynamic interactions with bounding surfaces stabilize either straight swimming against the flow or tumbling close to the channel wall, while pushers always move on a swinging trajectory with a specific amplitude as limit cycle.

  10. Vortices revealed: Swimming faster

    NASA Astrophysics Data System (ADS)

    van Houwelingen, Josje; van de Water, Willem; Kunnen, Rudie; van Heijst, Gertjan; Clercx, Herman

    2016-11-01

    Understanding and optimizing the propulsion in human swimming requires insight into the hydrodynamics of the flow around the swimmer. Experiments and simulations addressing the hydrodynamics of swimming have been conducted in studies before, including the visualization of the flow using particle image velocimetry (PIV). The main objective in this study is to develop a system to visualize the flow around a swimmer in practice inspired by this technique. The setup is placed in a regular swimming pool. The use of tracer particles and lasers to illuminate the particles is not allowed. Therefore, we choose to work with air bubbles with a diameter of 4 mm, illuminated by ambient light. Homogeneous bubble curtains are produced by tubes implemented in the bottom of the pool. The bubble motion is captured by six cameras placed in underwater casings. A first test with the setup has been conducted by pulling a cylinder through the bubbles and performing a PIV analysis. The vorticity plots of the resulting data show the expected vortex street behind the cylinder. The shedding frequency of the vortices resembles the expected frequency. Thus, it is possible to identify and follow the coherent structures. We will discuss these results and the first flow measurements around swimmers.

  11. Interspecific variation in hypoxia tolerance, swimming performance and plasticity in cyprinids that prefer different habitats.

    PubMed

    Fu, Shi-Jian; Fu, Cheng; Yan, Guan-Jie; Cao, Zhen-Dong; Zhang, An-Jie; Pang, Xu

    2014-02-15

    This study quantified and compared hypoxia tolerance and swim performance among cyprinid fish species from rapid-, slow- and intermediate-flow habitats (four species per habitat) in China. In addition, we explored the effects of short-term acclimation on swim performance, maximum metabolic rate (M(O2,max)) and gill remodelling to detect habitat-associated patterns of plastic response to hypoxia. Indices of hypoxia tolerance included oxygen threshold for loss of equilibrium (LOE50) and aquatic surface respiration (ASR50), and critical oxygen tension for routine metabolic rate (Pcrit). Critical swimming speed (Ucrit) and M(O2,max) were measured under normoxic and hypoxic conditions after 48 h acclimation to normoxia and hypoxia, and gill remodelling was estimated after 48 h of hypoxia exposure. Both traditional ANCOVA and phylogenetically independent contrast (PDANOVA) analyses showed that fish species from rapid-flow habitats exhibited lower LOE50 compared with fish from intermediate- and slow-flow habitats. Habitat-specific differences in Pcrit and Ucrit were detected using PDANOVA but not traditional ANCOVA analyses, with fish species from rapid-flow habitats exhibiting lower Pcrit but higher Ucrit values compared with fish from intermediate- and slow-flow habitats. Fish species from rapid-flow habitats were also characterized by less plasticity in swim performance and gill morphology in response to hypoxia acclimation compared with species from slow-flow habitats, but a greater drop in swim performance in response to acute hypoxia exposure. The study detected a habitat-specific difference in hypoxia tolerance, swimming performance and its plasticity among fish from habitats with different flow conditions, possibly because of the long-term adaptation to the habitat caused by selection stress. The PDANOVA analyses were more powerful than traditional statistical analyses according to the habitat effects in both hypoxia tolerance and swimming performance in this

  12. Disease resistance is related to inherent swimming performance in Atlantic salmon

    PubMed Central

    2013-01-01

    Background Like humans, fish can be classified according to their athletic performance. Sustained exercise training of fish can improve growth and physical capacity, and recent results have documented improved disease resistance in exercised Atlantic salmon. In this study we investigated the effects of inherent swimming performance and exercise training on disease resistance in Atlantic salmon. Atlantic salmon were first classified as either poor or good according to their swimming performance in a screening test and then exercise trained for 10 weeks using one of two constant-velocity or two interval-velocity training regimes for comparison against control trained fish (low speed continuously). Disease resistance was assessed by a viral disease challenge test (infectious pancreatic necrosis) and gene expression analyses of the host response in selected organs. Results An inherently good swimming performance was associated with improved disease resistance, as good swimmers showed significantly better survival compared to poor swimmers in the viral challenge test. Differences in mortalities between poor and good swimmers were correlated with cardiac mRNA expression of virus responsive genes reflecting the infection status. Although not significant, fish trained at constant-velocity showed a trend towards higher survival than fish trained at either short or long intervals. Finally, only constant training at high intensity had a significant positive effect on fish growth compared to control trained fish. Conclusions This is the first evidence suggesting that inherent swimming performance is associated with disease resistance in fish. PMID:23336751

  13. Reduced swim performance and aerobic capacity in adult zebrafish exposed to waterborne selenite.

    PubMed

    Massé, Anita J; Thomas, Jith K; Janz, David M

    2013-04-01

    Although dietary exposure of adult fish to organoselenium in contaminated aquatic ecosystems has been reported to bioaccumulate and cause larval deformities in offspring, subtle physiological effects produced through low level waterborne selenium exposure in fish such as swim performance and aerobic capacity have not been investigated. To evaluate potential effects of selenite on these responses, adult zebrafish (Danio rerio) were exposed to nominal aqueous concentrations of 0, 10 or 100 μg/L sodium selenite for 14 days. Upon completion of the exposure period, fish underwent two successive swim trials in a swim tunnel respirometer to determine critical swim speed (Ucrit), oxygen consumption (MO2), standard and active metabolic rates, aerobic scope (AS) and cost of transport (COT) followed by analysis of whole body triglyceride and glycogen concentrations. Selenite exposure had a significant negative effect on Ucrit and aerobic capacity. Active metabolic rates and AS significantly decreased in both selenite exposure groups after the second swim trial. No significant effect was observed in MO2, standard metabolic rate, COT, triglyceride and glycogen levels, or condition factor between groups. These results suggest that aqueous selenite exposure at environmentally relevant concentrations produces adverse effects on aerobic capacity that can diminish endurance and maximum swim speeds, which may lower fish survivability.

  14. Swimming of a Microrobot Actuated by a Clinical Magnetic Resonance Imaging Apparatus

    NASA Astrophysics Data System (ADS)

    Gosselin, Frederck P.; Zhou, David; Lalande, Viviane; Vonthron, Manuel; Martel, Sylvain

    2010-11-01

    A miniature robot was designed to achieve fish-like locomotion when actuated by the imaging coils of a clinical Magnetic Resonance Imaging (MRI) system. The wireless fish robot is composed of a ferromagnetic head, a flexible tail and a float. In an aquarium placed in the MRI, the robot is set into a swimming motion by an alternating transverse linear magnetic gradient. The influence of tail length, forcing frequency and forcing magnitude on the swimming velocity and flapping amplitude are investigated. Moreover, by using a combination of simultaneous magnetic gradients, the fish can reach superior swimming speeds than can be achieved by simply "pulling" on the fish with a magnetic field. Upon further miniaturization, the propulsion principle devised here could be used to navigate a micro surgical robot or a drug delivery system. A great advantage of this system is that no energy storage, motor or control system need to be carried by the robot, allowing great miniaturization possibilities.

  15. Establishing Zebrafish as a Novel Exercise Model: Swimming Economy, Swimming-Enhanced Growth and Muscle Growth Marker Gene Expression

    PubMed Central

    Rovira, Mireia; Brittijn, Sebastiaan A.; Burgerhout, Erik; van den Thillart, Guido E. E. J. M.; Spaink, Herman P.; Planas, Josep V.

    2010-01-01

    Background Zebrafish has been largely accepted as a vertebrate multidisciplinary model but its usefulness as a model for exercise physiology has been hampered by the scarce knowledge on its swimming economy, optimal swimming speeds and cost of transport. Therefore, we have performed individual and group-wise swimming experiments to quantify swimming economy and to demonstrate the exercise effects on growth in adult zebrafish. Methodology/Principal Findings Individual zebrafish (n = 10) were able to swim at a critical swimming speed (Ucrit) of 0.548±0.007 m s−1 or 18.0 standard body lengths (BL) s−1. The optimal swimming speed (Uopt) at which energetic efficiency is highest was 0.396±0.019 m s−1 (13.0 BL s−1) corresponding to 72.26±0.29% of Ucrit. The cost of transport at optimal swimming speed (COTopt) was 25.23±4.03 µmol g−1 m−1. A group-wise experiment was conducted with zebrafish (n = 83) swimming at Uopt for 6 h day−1 for 5 days week−1 for 4 weeks vs. zebrafish (n = 84) that rested during this period. Swimming zebrafish increased their total body length by 5.6% and body weight by 41.1% as compared to resting fish. For the first time, a highly significant exercise-induced growth is demonstrated in adult zebrafish. Expression analysis of a set of muscle growth marker genes revealed clear regulatory roles in relation to swimming-enhanced growth for genes such as growth hormone receptor b (ghrb), insulin-like growth factor 1 receptor a (igf1ra), troponin C (stnnc), slow myosin heavy chain 1 (smyhc1), troponin I2 (tnni2), myosin heavy polypeptide 2 (myhz2) and myostatin (mstnb). Conclusions/Significance From the results of our study we can conclude that zebrafish can be used as an exercise model for enhanced growth, with implications in basic, biomedical and applied sciences, such as aquaculture. PMID:21217817

  16. Directional swimming in bacteria: active and passive gradient responses

    NASA Astrophysics Data System (ADS)

    Stocker, Roman

    2012-02-01

    The ability to swim directionally is paramount for bacteria, in their quest for nutrients and favorable microhabitats. This ability depends on both active and passive responses to gradients. Here we bring an example from each case, based on novel microfluidic experiments that quantify the swimming behavior of bacteria. First, we describe their active response to oxygen gradients - or aerotaxis - and show the unexpected consequences of competing oxygen gradients with nutrient gradients. Then, we present the first observations of directional swimming by bacteria in response to fluid velocity gradients - or rheotaxis. Combining experiments with mathematical modeling we demonstrate that, unlike in larger organisms such as fish, rheotaxis in bacteria is passive, resulting from a previously undetected torque that originates from the chirality of the bacterial flagellum.

  17. Numerical simulations of undulatory swimming at moderate Reynolds number.

    PubMed

    Eldredge, Jeff D

    2006-12-01

    We perform numerical simulations of the swimming of a three-linkage articulated system in a moderately viscous regime. The computational methodology focuses on the creation, diffusion and transport of vorticity from the surface of the bodies into the fluid. The simulations are dynamically coupled, in that the motion of the three-linkage swimmer is computed simultaneously with the dynamics of the fluid. The novel coupling scheme presented in this work is the first to exploit the relationship between vorticity creation and body dynamics. The locomotion of the system, when subject to undulatory inputs of the hinges, is computed at Reynolds numbers of 200 and 1000. It is found that the forward swimming speed increases with the Reynolds number, and that in both cases the swimming is slower than in an inviscid medium. The vortex shedding is examined, and found to exhibit behavior consistent with experimental flow visualizations of fish.

  18. Partitioning of oxygen uptake and cost of surfacing during swimming in the air-breathing catfish Pangasianodon hypophthalmus.

    PubMed

    Lefevre, Sjannie; Wang, Tobias; Huong, Do Thi Thanh; Phuong, Nguyen Thanh; Bayley, Mark

    2013-02-01

    Though air-breathing has probably evolved mainly as a response to hypoxia, it may provide an important oxygen supplement when metabolism is elevated, as for example during swimming. Due to the increased travelling distance involved when an air-breathing fish swims to and from the surface, and the increased drag when the surface is breached, it can be proposed that air-breathing results in a rise in the apparent cost of transport. In order to investigate this hypothesis, it is necessary to use a fish that is able to swim equally well with and without access to air. The striped catfish Pangasianodon hypophthalmus has been shown to have a sufficiently high capacity for aquatic oxygen uptake in normoxia, to allow for such a comparison. Here, we measured the partitioning of oxygen uptake (MO2) during swimming and recovery, and calculated the apparent cost of transport with and without access to air, under normoxic conditions. Aerial MO2 constituted 25-40 % of the total MO2 during swimming and less than 15 % during recovery. The net cost of transport was 25 % lower in fish that did not air-breathe compared to fish that did, showing that the cost of surfacing can be substantial. This is the first study to measure partitioning in an air-breathing fish during swimming at velocities close to the critical swimming speed.

  19. Swimming in a crystal.

    PubMed

    Brown, Aidan T; Vladescu, Ioana D; Dawson, Angela; Vissers, Teun; Schwarz-Linek, Jana; Lintuvuori, Juho S; Poon, Wilson C K

    2016-01-07

    We study catalytic Janus particles and Escherichia coli bacteria swimming in a two-dimensional colloidal crystal. The Janus particles orbit individual colloids and hop between colloids stochastically, with a hopping rate that varies inversely with fuel (hydrogen peroxide) concentration. At high fuel concentration, these orbits are stable for 100s of revolutions, and the orbital speed oscillates periodically as a result of hydrodynamic, and possibly also phoretic, interactions between the swimmer and the six neighbouring colloids. Motile E. coli bacteria behave very differently in the same colloidal crystal: their circular orbits on plain glass are rectified into long, straight runs, because the bacteria are unable to turn corners inside the crystal.

  20. Creatine supplementation and swimming performance.

    PubMed

    Leenders, N M; Lamb, D R; Nelson, T E

    1999-09-01

    The purpose of this study was to determine if oral creatine (CR) ingestion, compared to a placebo (PL), would enable swimmers to maintain a higher swimming velocity across repeated interval sets over 2 weeks of supplementation. Fourteen female and 18 male university swimmers consumed a PL during a 2-week baseline period. Using a randomized, double-blind design, during the next 2 weeks subjects consumed either CR or PL. Swimming velocity was assessed twice weekly during 6 X 50-m swims and once weekly during 10 X 25-yd swims. There was no effect of CR on the 10 X 25-yd interval sets for men and women and no effect on the 6 X 50-m interval sets for women. In contrast, for men, CR significantly improved mean overall swimming velocity in the 6 X 50-m interval after 2 weeks of supplementation, whereas PL had no effect. Although ineffective in women, CR supplementation apparently enables men to maintain a faster mean overall swimming velocity during repeated swims each lasting about 30 s; however, CR was not effective for men in repeated swims each lasting about 10 - 15 s.

  1. Paramecia swimming in viscous flow

    NASA Astrophysics Data System (ADS)

    Zhang, P.; Jana, S.; Giarra, M.; Vlachos, P. P.; Jung, S.

    2015-12-01

    Ciliates like Paramecia exhibit fore-aft asymmetry in their body shapes, and preferentially swim in the direction of the slender anterior rather than the wider posterior. However, the physical reasons for this preference are not well understood. In this work, we propose that specific features of the fluid flow around swimming Paramecia confer some energetic advantage to the preferred swimming direction. Therefore, we seek to understand the effects of body asymmetry and swimming direction on the efficiency of swimming and the flux of fluid into the cilia layer (and thus of food into the oral groove), which we assumed to be primary factors in the energy budgets of these organisms. To this end, we combined numerical techniques (the boundary element method) and laboratory experiments (micro particle image velocimetry) to develop a quantitative model of the flow around a Paramecium and investigate the effect of the body shape on the velocity fields, as well as on the swimming and feeding behaviors. Both simulation and experimental results show that velocity fields exhibit fore-aft asymmetry. Moreover, the shape asymmetry revealed an increase of the fluid flux into the cilia layer compared to symmetric body shapes. Under the assumption that cilia fluid intake and feeding efficiency are primary factors in the energy budgets of Paramecia, our model predicts that the anterior swimming direction is energetically favorable to the posterior swimming direction.

  2. Physostomous channel catfish, Ictalurus punctatus, modify swimming mode and buoyancy based on flow conditions.

    PubMed

    Yoshida, Makoto A; Yamamoto, Daisuke; Sato, Katsufumi

    2017-02-15

    The employment of gliding in aquatic animals as a means of conserving energy has been theoretically predicted and discussed for decades. Several studies have shown that some species glide, whereas others do not. Freshwater fish species that widely inhabit both lentic and lotic environments are thought to be able to adapt to fluctuating flow conditions in terms of locomotion. In adapting to the different functional demands of lentic and lotic environments on fish energetics, physostomous (open swim bladder) fish may optimise their locomotion and activity by controlling their net buoyancy; however, few buoyancy studies have been conducted on physostomous fish in the wild. We deployed accelerometers on free-ranging channel catfish, Ictalurus punctatus, in both lentic and lotic environments to quantify their swimming activity, and to determine their buoyancy condition preferences and whether gliding conserves energy. Individual comparisons of swimming efforts between ascent and descent phases revealed that all fish in the lentic environment had negative buoyancy. However, all individuals showed many descents without gliding phases, which was contrary to the behaviour predicted to minimise the cost of transport. The fact that significantly fewer gliding phases were observed in the lotic environment, together with the existence of neutrally buoyant fish, indicated that channel catfish seem to optimise their locomotion through buoyancy control based on flow conditions. The buoyancy optimisation of channel catfish relative to the flow conditions that they inhabit not only reflects differences in swimming behaviour but also provides new insights into the adaptation of physostome fish species to various freshwater environments.

  3. On the hydrodynamics of fish schooling

    NASA Astrophysics Data System (ADS)

    Borazjani, Iman; Daghooghi, Mohsen

    2013-11-01

    A Considerable number of fish species swim in a coordinated manner within approximately constant and equal distance from each other, forming a pattern which is referred to as a fish school. It is believed that fish schooling results in more efficient swimming. However, no experimental evidence has conclusively shown the hydrodynamic effects of neighboring fish on swimming, probably due to the challenges involved in measuring the performance under controlled conditions in a school. We investigate possible hydrodynamical effects of fish schooling by constructing an infinite school of virtual swimmers based on a mackerel fish body and carangiform kinematics. We carry out our self-propelled simulation based on prescribed undulations of the fish body (assuming that all of the fish in the school move in exact same manner) and calculating motion of the center of mass. One of the most important geometrical factors of the fish schooling pattern seems to be the distance between two adjacent fish in the school. Therefore, we examined fish schools with different distances of two adjacent fish. This work was partly supported by the Center for Computational Research (CCR), University at Buffalo.

  4. Use of electromyogram telemetry to assess swimming activity of adult spring Chinook salmon migrating past a Columbia River dam

    USGS Publications Warehouse

    Brown, R.S.; Geist, D.R.; Mesa, M.G.

    2006-01-01

    Electromyogram (EMG) radiotelemetry was used to estimate the swim speeds of spring Chinook salmon Oncorhynchus tshawytscha migrating upstream past a Columbia River dam. Electrodes from EMG transmitters were surgically implanted in the red muscle of fish captured at Bonneville Dam, and output from the tags was calibrated to defined swim speeds for each fish in a tunnel respirometer. The fish were then released below Bonneville Dam and radio-tracked as they migrated through the tailraces, fishways, and forebays of the dam. On average, swim speed was significantly higher when tagged salmon were moving through tailraces than when they were moving through other parts of the dam. Specifically, swim speeds for fish in tailraces (106.4 cm/s) were 23% higher than those of fish in fishways (84.9 cm/s) and 32% higher than those of fish in forebays (80.2 cm/s). Swim speeds were higher in fishways during the day than during the night, but there were no diel differences in swim speeds in tailraces and forebays. During dam passage, Chinook salmon spent the most time in tailraces, followed by fishways and forebays. ?? Copyright by the American Fisheries Society 2006.

  5. Swimming Microrobot Optical Nanoscopy.

    PubMed

    Li, Jinxing; Liu, Wenjuan; Li, Tianlong; Rozen, Isaac; Zhao, Jason; Bahari, Babak; Kante, Boubacar; Wang, Joseph

    2016-10-12

    Optical imaging plays a fundamental role in science and technology but is limited by the ability of lenses to resolve small features below the fundamental diffraction limit. A variety of nanophotonic devices, such as metamaterial superlenses and hyperlenses, as well as microsphere lenses, have been proposed recently for subdiffraction imaging. The implementation of these micro/nanostructured lenses as practical and efficient imaging approaches requires locomotive capabilities to probe specific sites and scan large areas. However, directed motion of nanoscale objects in liquids must overcome low Reynolds number viscous flow and Brownian fluctuations, which impede stable and controllable scanning. Here we introduce a new imaging method, named swimming microrobot optical nanoscopy, based on untethered chemically powered microrobots as autonomous probes for subdiffraction optical scanning and imaging. The microrobots are made of high-refractive-index microsphere lenses and powered by local catalytic reactions to swim and scan over the sample surface. Autonomous motion and magnetic guidance of microrobots enable large-area, parallel and nondestructive scanning with subdiffraction resolution, as illustrated using soft biological samples such as neuron axons, protein microtubulin, and DNA nanotubes. Incorporating such imaging capacities in emerging nanorobotics technology represents a major step toward ubiquitous nanoscopy and smart nanorobots for spectroscopy and imaging.

  6. Drag on swimming flexible foils

    NASA Astrophysics Data System (ADS)

    Raspa, Veronica; Ramananarivo, Sophie; Thiria, Benjamin; Godoy-Diana, Ramiro

    2013-11-01

    We study experimentally the swimming dynamics of thin flexible foils in a self-propelled configuration. Measurements of swimming speed and propulsive force are performed, together with full recordings of the elastic wave kinematics and particle image velocimetry around the swimming foils. We discuss the general problem of drag in undulatory swimming using a bluff-body type model. Our results suggest that a major contribution to the total drag is due to the trailing longitudinal vortices that roll-up on the lateral edges of the foil. Additionally, changing the aspect ratio of the foils allows us to discuss quantitatively the role of the added mass term in Lighthill's elongated-body theory for thrust production in undulatory swimming. We acknowledge support by EADS Foundation through project ``Fluids and elasticity in biomimetic propulsion.''

  7. Lake Erie...A Day in the Life of a Fish.

    ERIC Educational Resources Information Center

    Canning, Maureen; Dunlevy, Margie

    This elementary school teaching unit was developed as a part of a series of units that deal with Lake Erie. This unit was developed to enable children to: (1) examine a moving fish; (2) conduct experiments with a live fish; (3) understand the swimming habits of fish; (4) learn how fish breathe; (5) recognize different methods of fish protection…

  8. Cardiorespiratory performance and blood chemistry during swimming and recovery in three populations of elite swimmers: Adult sockeye salmon.

    PubMed

    Eliason, Erika J; Clark, Timothy D; Hinch, Scott G; Farrell, Anthony P

    2013-10-01

    Every year, millions of adult sockeye salmon (Oncorhynchus nerka) perform an arduous, once-in-a-lifetime migration up the Fraser River (BC, Canada) to return to their natal stream to spawn. The changes in heart rate, stroke volume, and arterio-venous oxygen extraction (i.e., factors determining rates of oxygen delivery to the tissues by the cardiovascular system) have never been directly and simultaneously measured along with whole animal oxygen uptake in a maximally swimming fish. Here, such measurements were made using three sockeye salmon populations (Early Stuart, Chilko and Quesnel), which each performed two consecutive critical swimming speed (Ucrit) challenges to provide a comprehensive quantification of cardiovascular physiology, oxygen status and blood chemistry associated with swimming and recovery. Swim performance, oxygen uptake, cardiac output, heart rate and stroke volume did not significantly vary at rest, during swimming or during recovery between populations or sexes. Despite incomplete metabolic recovery between swim challenges, all fish repeated their swim performance and similar quantitative changes in the cardiorespiratory variables were observed for each swim challenge. The high maximum cardiorespiratory performance and excellent repeat swim performance are clearly beneficial in allowing the salmon to maintain steady ground speeds and reach the distant spawning grounds in a timely manner.

  9. The determination of the swimming performance of rainbow trout (Oncorhynchus mykiss) under the effect of detergent

    NASA Astrophysics Data System (ADS)

    Esenbuǧa, Hülya; Alak, Gonca; Atamanalp, Muhammed

    2017-04-01

    Detergent residues can lead to continuous damage in the cell membranes and make them become sensitive to the harmful effects of other toxic substances and infection factors. In this study, the behavioral responses of rainbow trout have been studied at the end of 21 days, where they have been exposed to different concentrations of Sodium Dodecyl Sulphate (SDS). In the fish which have been exposed to two different doses of SDS material, the swimming performance has been examined for behavior analysis with emphasis on critical swimming speed. The effect of SDS on critical swimming speed has been found to be significant (p <0.05).

  10. Swim bladder function and buoyancy control in pink snapper (Pagrus auratus) and mulloway (Argyrosomus japonicus).

    PubMed

    Stewart, John; Hughes, Julian M

    2014-04-01

    Physoclist fish are able to regulate their buoyancy by secreting gas into their hydrostatic organ, the swim bladder, as they descend through the water column and by resorbing gas from their swim bladder as they ascend. Physoclists are restricted in their vertical movements due to increases in swim bladder gas volume that occur as a result of a reduction in hydrostatic pressure, causing fish to become positively buoyant and risking swim bladder rupture. Buoyancy control, rates of swim bladder gas exchange and restrictions to vertical movements are little understood in marine teleosts. We used custom-built hyperbaric chambers and laboratory experiments to examine these aspects of physiology for two important fishing target species in southern Australia, pink snapper (Pagrus auratus) and mulloway (Argyrosomus japonicus). The swim bladders of pink snapper and mulloway averaged 4.2 and 4.9 % of their total body volumes, respectively. The density of pink snapper was not significantly different to the density of seawater (1.026 g/ml), whereas mulloway were significantly denser than seawater. Pink snapper secreted gas into their swim bladders at a rate of 0.027 ± 0.005 ml/kg/min (mean ± SE), almost 4 times faster than mulloway (0.007 ± 0.001 ml/kg/min). Rates of swim bladder gas resorption were 11 and 6 times faster than the rates of gas secretion for pink snapper and mulloway, respectively. Pink snapper resorbed swim bladder gas at a rate of 0.309 ± 0.069 ml/kg/min, 7 times faster than mulloway (0.044 ± 0.009 ml/kg/min). Rates of gas exchange were not affected by water pressure or water temperature over the ranges examined in either species. Pink snapper were able to acclimate to changes in hydrostatic pressure reasonably quickly when compared to other marine teleosts, taking approximately 27 h to refill their swim bladders from empty. Mulloway were able to acclimate at a much slower rate, taking approximately 99 h to refill their swim bladders. We estimated that the

  11. Self-entrainment to optimal gaits of an underactuated biomimetic swimming robot using adaptive frequency oscillators.

    PubMed

    Alessi, Alessio; Accoto, Dino; Guglielmelli, Eugenio

    2015-08-01

    Underactuated compliant swimming robots are characterized by a simple mechanical structure, capable to mimic the body undulation of many fish species. One of the design issue for these robots is the generation and control of best performing swimming gaits. In this paper we propose a new controller, based on AFO oscillators, to address this issue. After analyzing the effects of the motion on the robot natural frequencies, we show that the closed loop system is able to generate self-sustained oscillations, at a characteristic frequency, while maximizing swimming velocity.

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

    PubMed

    Marit, Jordan S; Weber, Lynn P

    2011-06-01

    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 LC₅₀. 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.

  13. Effects of Acoustic Transmitters on the Swimming Performance and Predator Avoidance of Juvenile Chinook Salmon

    SciTech Connect

    Anglea, Steven M.; Geist, David R.; Brown, Richard S.; Deters, Katherine A.; Mcdonald, Robert D.

    2004-03-01

    The objective of this study was to determine if juvenile chinook salmon (Oncorhynchus tshawytscha) were negatively influenced by the implantation of acoustic transmitters. The critical swimming speed (Ucrit) of tagged fish, sham (surgery but no tag), and control fish was measured in a respirometer to determine tag effects on swimming performance. Predator avoidance was evaluated by comparing the proportion of each treatment group eaten: active tag, inactive tag, sham, and control after being exposed to piscivorous adult rainbow trout (O. mykiss). Results from this study demonstrated that the surgical implantation of acoustic tags in juvenile fall chinook salmon does not significantly affect swimming performance. Swimming performance was similar between treatment groups (control, sham, and inactive tag) at 1- and 21-day post-surgery intervals. Critical swimming speeds for all treatment groups were similar to values reported in the literature. Implantation of acoustic transmitters (active and inactive) did not result in tagged fish being more susceptible to predation over untagged fish. Percentages of each prey group consumed in each of the four trials were highly variable and demonstrated no obvious selection preference by adult rainbow trout. In summary, measurable differences were not found between tagged and un-tagged fish, however, trends were consistent in the two experiments with tagged fish consistently performing slightly worse than un-tagged fish. We conclude that based on the current body of knowledge and findings of the present study, fish implanted with an acoustic tag perform and/or behave similarly to the population-at-large recognizing that subtle differences exist in the behavior of tagged fish.

  14. Functional morphology and hydrodynamics of backward swimming in bluegill sunfish, Lepomis macrochirus.

    PubMed

    Flammang, Brooke E; Lauder, George V

    2016-10-01

    Most teleost fishes, like the bluegill sunfish Lepomis macrochirus, have multiple flexible fins that are used as modifiable control surfaces. This helps to make fish highly maneuverable, permitting behaviors like reversing direction of motion and swimming backwards without having to rotate body position. To answer the question of how fish swim backwards we used high-speed videography and electromyography to determine the kinematics and muscle activity necessary to produce reverse-direction propulsion in four bluegill sunfish. We found that, in contrast to slow forward swimming, low-speed backward swimming is a multi-fin behavior, utilizing the pectoral, dorsal, anal, and caudal fins. The pectoral fins alternate beats, each fin broadly flaring on the outstroke and feathered on the instroke. The dorsal fin and dorsal portion of the caudal fin move out of phase as do the anal fin and ventral portion of the caudal fin. Electromyography of muscles in the pectoral, dorsal, anal, and caudal fins demonstrated bilateral activation when these fins changed direction, suggesting that fins are stiffened at this time. In addition to backward propulsion by the pectoral fins, particle image velocimetry revealed that the dorsal and anal fins are capable of producing reverse momentum jets to propel the fish backward. Because teleost fishes are statically unstable, locomotion at slow speeds requires precise fin control to adequately balance torques produced about the center of mass. Therefore, the kinematics of backward swimming may be the result of compensation for rolling, pitching, and yawning instability. We suggest that asymmetric pectoral fin activity with feathering during adduction balances rolling instability. The ventral to dorsal undulatory wave on the caudal fin controls pitch instability and yaw instability encountered from pectoral-driven backward locomotion. Thrust generation from the dorsal and anal fins decreases the destabilizing effect of the long moment arm of the

  15. Strouhal numbers and optimization of swimming by odontocete cetaceans.

    PubMed

    Rohr, Jim J; Fish, Frank E

    2004-04-01

    Swimming efficiencies of fish and cetaceans have been related to a certain synchrony between stroke cycle frequency, peak-to-peak tail/fluke amplitude and mean swimming speed. These kinematic parameters form a non-dimensional wake parameter, referred to as a Strouhal number, which for the range between 0.20 and 0.40 has been associated with enhanced swimming efficiency for fish and cetaceans. Yet to date there has been no direct experimental substantiation of what Strouhal numbers are preferred by swimming cetaceans. To address this lack of data, a total of 248 Strouhal numbers were calculated for the captive odontocete cetaceans Tursiops truncatus, Pseudorca crassidens, Orcinus orca, Globicephala melaena, Lagenorhynchus obliquidens and Stenella frontalis. Although the average Strouhal number calculated for each species is within the accepted range, considerable scatter is found in the data both within species and among individuals. A greater proportion of Strouhal values occur between 0.20 and 0.30 (74%) than the 0.25-0.35 (55%) range predicted for maximum swimming efficiency. Within 0.05 Strouhal increments, the greatest number of Strouhal values was found between 0.225 and 0.275 (44%). Where propulsive efficiency data were available (Tursiops truncatus, Pseudorca crassidens, Orcinus orca), peak swimming efficiency corresponded to this same Strouhal range. The odontocete cetacean data show that, besides being generally limited to a range of Strouhal numbers between 0.20 and 0.40, the kinematic parameters comprising the Strouhal number provide additional constraints. Fluke-beat frequency normalized by the ratio of swimming speed to body length was generally restricted from 1 to 2, whereas peak-to-peak fluke amplitude normalized by body length occurred predominantly between 0.15 and 0.25. The results indicate that the kinematics of the propulsive flukes of odontocete cetaceans are not solely dependent on Strouhal number, and the Strouhal number range for odontocete

  16. Volumetric imaging of fish locomotion

    PubMed Central

    Flammang, Brooke E.; Lauder, George V.; Troolin, Daniel R.; Strand, Tyson E.

    2011-01-01

    Fishes use multiple flexible fins in order to move and maintain stability in a complex fluid environment. We used a new approach, a volumetric velocimetry imaging system, to provide the first instantaneous three-dimensional views of wake structures as they are produced by freely swimming fishes. This new technology allowed us to demonstrate conclusively the linked ring vortex wake pattern that is produced by the symmetrical (homocercal) tail of fishes, and to visualize for the first time the three-dimensional vortex wake interaction between the dorsal and anal fins and the tail. We found that the dorsal and anal fin wakes were rapidly (within one tail beat) assimilated into the caudal fin vortex wake. These results show that volumetric imaging of biologically generated flow patterns can reveal new features of locomotor dynamics, and provides an avenue for future investigations of the diversity of fish swimming patterns and their hydrodynamic consequences. PMID:21508026

  17. Volumetric imaging of fish locomotion.

    PubMed

    Flammang, Brooke E; Lauder, George V; Troolin, Daniel R; Strand, Tyson E

    2011-10-23

    Fishes use multiple flexible fins in order to move and maintain stability in a complex fluid environment. We used a new approach, a volumetric velocimetry imaging system, to provide the first instantaneous three-dimensional views of wake structures as they are produced by freely swimming fishes. This new technology allowed us to demonstrate conclusively the linked ring vortex wake pattern that is produced by the symmetrical (homocercal) tail of fishes, and to visualize for the first time the three-dimensional vortex wake interaction between the dorsal and anal fins and the tail. We found that the dorsal and anal fin wakes were rapidly (within one tail beat) assimilated into the caudal fin vortex wake. These results show that volumetric imaging of biologically generated flow patterns can reveal new features of locomotor dynamics, and provides an avenue for future investigations of the diversity of fish swimming patterns and their hydrodynamic consequences.

  18. Baby swimming and respiratory health.

    PubMed

    Nystad, Wenche; Håberg, Siri E; London, Stephanie J; Nafstad, Per; Magnus, Per

    2008-05-01

    To estimate the effect of baby swimming in the first 6 months of life on respiratory diseases from 6 to 18 months. We used data from The Norwegian Mother and Child Cohort Study (MoBa) conducted by the Norwegian Institute of Public Health in children born between 1999 and 2005 followed from birth to the age of 18 months (n = 30,870). Health outcomes: lower respiratory tract infections (LRTI), wheeze and otitis media between 6 and 18 months of age. baby swimming at the age of 6 months. The effect of baby swimming was estimated by logistic regression analysis adjusting for potential confounders. About 25% of the children participated in baby swimming. The prevalence of LRTI was 13.3%, wheeze 40.0% and otitis media 30.4%. Children who were baby swimming were not more likely to have LRTI, to wheeze or to have otitis media. However, children with atopic mothers who attended baby swimming had an increased risk of wheeze, adjusted odds ratios (aOR) 1.24 (95% CI 1.11, 1.39), but not LRTI or otitis media. This was also the case for children without respiratory diseases before 6 months aOR 1.08 (95%CI 1.02-1.15). Baby swimming may be related to later wheeze. However, these findings warrant further investigation.

  19. Baby swimming and respiratory health

    PubMed Central

    Nystad, Wenche; Håberg, Siri E.; London, Stephanie J; Nafstad, Per; Magnus, Per

    2010-01-01

    Aim To estimate the effect of baby swimming the first six months of life on respiratory diseases from 6 to 18 months. Methods We used data from The Norwegian Mother and Child Cohort Study (MoBa) conducted by the Norwegian Institute of Public Health in children born 1999 – 2005 followed from birth to the age of 18 months (n = 30,870). Health outcomes: lower respiratory tract infections (LRTI), wheeze and otitis media between 6 and 18 months of age. Exposure: baby swimming at age 6 months. The effect of baby swimming was estimated by logistic regression analysis adjusting for potential confounders. Results About 25% of the children participated in baby swimming. The prevalence of LRTI was 13.3%, wheeze 40.0% and otitis media 30.4%. Children who were baby swimming were not more likely to have LRTI, to wheeze or to have otitis media. However, children with atopic mothers who attended baby swimming had an increased risk of wheeze, aOR 1.24 (95% CI 1.11, 1.39), but not LRTI or otitis media. This was also the case for children without respiratory diseases before 6 months aOR 1.08 (95%CI 1.02–1.15). Conclusion Baby swimming may be related to later wheeze. However, these findings warrant further investigation. PMID:18394113

  20. On the hydrodynamics of fishlike swimming: Anguilliform vs. Carangiform locomotion

    NASA Astrophysics Data System (ADS)

    Borazjani, Iman; Sotiropoulos, Fotis

    2008-11-01

    Comparing anguilliform and carangiform swimming experimentally is a great challenge due to issues such as obtaining 3D flow and pressure fields around the live fish, control over the live fish, etc. Numerical simulations can be a powerful tool to complement experiments in this respect. We carry out a systematic numerical study to compare virtual anguilliform and carangiform swimmers. Using simulations for tethered virtual swimmers we study the effects of Reynolds number (Re) on swimming performance. We found that the carangiform swimmers' efficiency increases as the Re increases while the anguilliform efficiency peaks in the transitional regime due to the difference in either kinematics or shape of the virtual swimmers. To study the effects of shape and kinematics separately, we perform a series of self-propelled simulations by prescribing the anguilliform kinematics on the carangiform body and vice versa. The computed results provide novel insights into the performance of each mode of swimming in various flow regimes and help reconcile and clarify experimental observations with live fish.

  1. To Swim or Not to Swim: Potential Transmission of Balaenophilus manatorum (Copepoda: Harpacticoida) in Marine Turtles

    PubMed Central

    Tomás, Jesús; Crespo-Picazo, José Luis; García-Párraga, Daniel; Raga, Juan Antonio

    2017-01-01

    Species of Balaenophilus are the only harpacticoid copepods that exhibit a widespread, obligate association with vertebrates, i.e., B. unisetus with whales and B. manatorum with marine turtles and manatees. In the western Mediterranean, juveniles of the loggerhead sea turtle, Caretta caretta are the only available hosts for B. manatorum, which has been found occurring at high prevalence (>80%) on them. A key question is how these epibionts are transmitted from host to host. We investigated this issue based on experiments with live specimens of B. manatorum that were cultured with turtle skin. Specimens were obtained from head-started hatchlings of C. caretta from the western Mediterranean. Hatched nauplii crawled only on rough substrates and lacked the ability to swim. Only copepodites IV and V, and adults, were able to perform directional swimming. Legs 2, 3 and 4 played a major role in swimming and were only well-developed in these stages. Nauplii reared in wells with turtle skin readily fed on this item. Late copepodites and adults also fed on turtle skin but did not consume other potential food items such as fish skin, baleen plates or planktonic algae. Evidences suggest that the transmission of B. manatorum should rely on hosts’ bodily contacts and/or swimming of late developmental stages between spatially close hosts. The possibility of long-ranged dispersal is unlikely for two reasons. First, all developmental stages seem to depend on turtle skin as a food resource. Second, the average clutch size of ovigerous females was small (< 70 eggs) for free-living phases to successfully contact turtles that occur at very low densities (< 0.6 turtles·km−2) in the western Mediterranean. The high prevalence of B. manatorum in loggerhead turtles in this area raises the question whether these turtles have contacts, or tend to closely aggregate, more than is currently believed. PMID:28114412

  2. 21 CFR 1250.89 - Swimming pools.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Swimming pools. 1250.89 Section 1250.89 Food and... SANITATION Sanitation Facilities and Conditions on Vessels § 1250.89 Swimming pools. (a) Fill and draw swimming pools shall not be installed or used. (b) Swimming pools of the recirculation type shall be...

  3. Swimming Performance and Metabolism of Golden Shiners

    USDA-ARS?s Scientific Manuscript database

    The swimming ability and metabolism of golden shiners, Notemigonus crysoleucas, was examined using swim tunnel respirometery. The oxygen consumption and tail beat frequencies at various swimming speeds, an estimation of the standard metabolic rate, and the critical swimming speed (Ucrit) was determ...

  4. 21 CFR 1250.89 - Swimming pools.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Swimming pools. 1250.89 Section 1250.89 Food and... SANITATION Sanitation Facilities and Conditions on Vessels § 1250.89 Swimming pools. (a) Fill and draw swimming pools shall not be installed or used. (b) Swimming pools of the recirculation type shall...

  5. 21 CFR 1250.89 - Swimming pools.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Swimming pools. 1250.89 Section 1250.89 Food and... SANITATION Sanitation Facilities and Conditions on Vessels § 1250.89 Swimming pools. (a) Fill and draw swimming pools shall not be installed or used. (b) Swimming pools of the recirculation type shall...

  6. Applying Mechanics to Swimming Performance Analysis.

    ERIC Educational Resources Information Center

    Barthels, Katharine

    1989-01-01

    Swimming teachers and coaches can improve their feedback to swimmers, when correcting or refining swim movements, by applying some basic biomechanical concepts relevant to swimming. This article focuses on the biomechanical considerations used in analyzing swimming performance. Techniques for spotting and correcting problems that impede…

  7. Swimming endurance of bull trout, lake trout, arctic char, and rainbow trout following challenge with Renibacterium salmoninarum

    USGS Publications Warehouse

    Jones, D.T.; Moffitt, C.M.

    2004-01-01

    We tested the swimming endurance of juvenile bull trout Salvelinus confluentus, lake trout S. namaycush, Arctic char S. alpinus, and rainbow trout Oncorhynchus mykiss at 9??C and 15??C to determine whether sublethal infection from a moderate challenge of Renibacterium salmoninarum administered months before testing affected the length of time fish could maintain a swimming speed of 5-6 body lengths per second in an experimental flume. Rainbow trout and Arctic char swam longer in trials than did bull trout or lake trout, regardless of challenge treatment. When we tested fish 14-23 weeks postchallenge, we found no measurable effect of R. salmoninarum on the swimming endurance of the study species except for bull trout, which showed a mixed response. We conducted additional trials with bull trout 5-8 weeks postchallenge to determine whether increasing the challenge dose would affect swimming endurance and hematocrit. In those tests, bull trout with clinical signs of disease and those exposed to the highest challenge doses had significantly reduced swimming endurance compared with unchallenged control fish. Fish hematocrit levels measured at the end of all swimming endurance tests varied among species and between test temperatures, and patterns were not always consistent between challenged and control fish.

  8. The physiology and biomechanics of competitive swimming.

    PubMed

    Troup, J P

    1999-04-01

    Fast swimming, either in the pool, in open water swimming, or in water polo and synchronized swimming, requires maximizing the efficiencies with which the human body can move through a liquid medium. A multitude of factors can affect the ability to swim fast as well as the final outcome. Physiology and biomechanics are the present tools used by sports scientists to determine which factors are important to fast swimming and, subsequently, to determine how the swimmer may maximize these factors to improve performance.

  9. Fish robotics and hydrodynamics

    NASA Astrophysics Data System (ADS)

    Lauder, George

    2010-11-01

    Studying the fluid dynamics of locomotion in freely-swimming fishes is challenging due to difficulties in controlling fish behavior. To provide better control over fish-like propulsive systems we have constructed a variety of fish-like robotic test platforms that range from highly biomimetic models of fins, to simple physical models of body movements during aquatic locomotion. First, we have constructed a series of biorobotic models of fish pectoral fins with 5 fin rays that allow detailed study of fin motion, forces, and fluid dynamics associated with fin-based locomotion. We find that by tuning fin ray stiffness and the imposed motion program we can produce thrust both on the fin outstroke and instroke. Second, we are using a robotic flapping foil system to study the self-propulsion of flexible plastic foils of varying stiffness, length, and trailing edge shape as a means of investigating the fluid dynamic effect of simple changes in the properties of undulating bodies moving through water. We find unexpected non-linear stiffness-dependent effects of changing foil length on self-propelled speed, and as well as significant effects of trailing edge shape on foil swimming speed.

  10. Effects of a Novel Acoustic Transmitter on Swimming Performance and Predator Avoidance of Juvenile Chinook Salmon: Determination of a Size Threshold

    SciTech Connect

    Walker, Ricardo W.; Ashton, Neil K.; Brown, Richard S.; Liss, Stephanie A.; Colotelo, Alison HA; Do Vale Beirao, Bernardo; Townsend, Richard L.; Deng, Zhiqun; Eppard, M. B.

    2016-01-04

    Abstract Telemetry studies are used worldwide to investigate the behavior and migration of fishes. The miniaturization of acoustic transmitters enables researchers to tag smaller fish, such as the juvenile life stages of salmon, thus representing a greater proportion of the population of interest. The development of an injectable acoustic transmitter has led to research determining the least invasive and quickest method of tag implantation. Swimming performance and predator avoidance were examined. To quantify critical swimming speed (Ucrit; an index of prolonged swimming performance) and predator avoidance for juvenile Chinook salmon (Oncorhynchus tshawytscha), fish were split into three groups: (1) fish implanted with a dummy injectable acoustic transmitter (IAT treatment), (2) fish implanted with a dummy injectable acoustic transmitter and passive integrated transponder (PIT) tag (IAT+PIT treatment), and (3) an untagged control group. The Ucrits and predator avoidance capability of tagged fish were compared with untagged fish to determine if carrying an IAT adversely affected swimming performance or predator avoidance. Fish implanted with only an IAT had lower Ucrit values than untagged fish and a size threshold at 79 mm fork length was found. Conversely, Ucrit values for fish implanted with an IAT+PIT were not significantly different from untagged controls and no size threshold was found. Predator avoidance testing showed no significant difference for fish implanted with an IAT compared to untagged individuals, nor was there a significant difference for IAT+PIT fish compared to untagged fish.

  11. Energy exchanges of swimming man

    NASA Technical Reports Server (NTRS)

    Nadel, E. R.; Holmer, I.; Bergh, U.; Astrand, P.-O.; Stolwijk, J. A. J.

    1974-01-01

    Three male swimmers underwent 10-min resting and 20-min swimming (breaststroke) exposures in a swimming flume. Water temperatures in separate exposures were 18, 26, and 33 C. At each water temperature the subjects rested and swam at water velocities of 0.50, 0.75, and 0.95 m/sec, which were designed to produce around 40, 70, and 100% of maximal aerobic power. Measurements were made of esophageal temperature, four skin temperatures, water temperature, heat flow from five local skin surfaces (Hatfield-Turner disks), and oxygen uptake. Calculations were made of mean area-weighted skin temperature and heat flow, metabolic rate, and heat storage. Internal body temperature changes after 20 min of swimming were related to water temperature, swimming intensity, and body composition.

  12. System Wide Information Management (SWIM)

    NASA Technical Reports Server (NTRS)

    Hritz, Mike; McGowan, Shirley; Ramos, Cal

    2004-01-01

    This viewgraph presentation lists questions regarding the implementation of System Wide Information Management (SWIM). Some of the questions concern policy issues and strategies, technology issues and strategies, or transition issues and strategies.

  13. Swimming Pools and Molluscum Contagiosum

    MedlinePlus

    ... to another if they share a towel or toys. Parents and others often ask if molluscum virus ... it can spread by sharing swimming equipment, pool toys, or towels. Some investigations report that spread of ...

  14. Fluid dynamics: Swimming across scales

    NASA Astrophysics Data System (ADS)

    Baumgart, Johannes; Friedrich, Benjamin M.

    2014-10-01

    The myriad creatures that inhabit the waters of our planet all swim using different mechanisms. Now, a simple relation links key physical observables of underwater locomotion, on scales ranging from millimetres to tens of metres.

  15. Energy exchanges of swimming man

    NASA Technical Reports Server (NTRS)

    Nadel, E. R.; Holmer, I.; Bergh, U.; Astrand, P.-O.; Stolwijk, J. A. J.

    1974-01-01

    Three male swimmers underwent 10-min resting and 20-min swimming (breaststroke) exposures in a swimming flume. Water temperatures in separate exposures were 18, 26, and 33 C. At each water temperature the subjects rested and swam at water velocities of 0.50, 0.75, and 0.95 m/sec, which were designed to produce around 40, 70, and 100% of maximal aerobic power. Measurements were made of esophageal temperature, four skin temperatures, water temperature, heat flow from five local skin surfaces (Hatfield-Turner disks), and oxygen uptake. Calculations were made of mean area-weighted skin temperature and heat flow, metabolic rate, and heat storage. Internal body temperature changes after 20 min of swimming were related to water temperature, swimming intensity, and body composition.

  16. Healthy Swimming/Recreational Water

    MedlinePlus

    ... Index of Water-Related Topics Featured Partners Healthy Water Sites Healthy Water Drinking Water Healthy Swimming Global WASH Other Uses of Water WASH-related Emergencies & Outbreaks Water, Sanitation, & Environmentally-related ...

  17. Relationships Between Metabolic Rate, Muscle Electromyograms and Swim Performance of Adult Chinook Salmon

    SciTech Connect

    Geist, David R.; Brown, Richard S.; Cullinan, Valerie I.; Mesa, Matthew G.; VanderKooi, S P.; McKinstry, Craig A.

    2003-10-01

    In 2000 Pacific Northwest National Laboratory initiated a two-year study to investigate the metabolic rate and swimming performance and to estimate the total energy used (i.e., aerobic and anaerobic) by adult spring Chinook salmon migrating upstream through a large hydropower dam on the Columbia River. The investigation involved one year of laboratory study and one year of field study at Bonneville Dam. The objectives of the laboratory study, reported here, were to (1) measure active rates of oxygen consumption of adult spring chinook salmon at three water temperatures over a range of swimming speeds; (2) estimate the Ucrit of adult spring chinook salmon; and (3) monitor EMGs of red and white muscle in the salmon over a range of swimming speeds. Future papers will report on the results of the field study. Our results indicated that the rate of oxygen consumption and red and white muscle activity in adult spring chinook salmon were strongly correlated with swimming speed over a range of fish sizes and at three different temperatures. Active oxygen consumption increased linearly with swim speed before leveling off at speeds at or above Ucrit. This pattern was similar at each water temperature and indicated that fish were approaching their maximal aerobic oxygen consumption at higher swim speeds. Modeling showed that temperature, but not size or sex, influenced the relation between V02 and swim speed, thus a V02-swim speed model based on temperature (but independent of sex and size) should be a biologically relevant way of estimating the energy use of fish in the wild.

  18. Orthopedic aspects of competitive swimming.

    PubMed

    Richardson, A B

    1987-07-01

    Orthopedic problems related to competitive swimming are rarely disabling, but can be problematic in preventing training and competition. Most problems are related to the shoulder and knee. Treatment is primarily nonsurgical and directed at relieving symptoms and allowing the athlete to continue with swimming practice. Treatment aids such as ice packing, anti-inflammatory medications, muscle stimulation and electrogalvanic stimulation, strengthening exercises, and static stretching are encouraged; upper arm bands and patellar-stabilizing supports can be adapted to training routines.

  19. Sustained Swimming Speeds of Dolphins.

    PubMed

    Johannessen, C L; Harder, J A

    1960-11-25

    Observations of fout large groups of dolphins suggest that they are able to swim at a sustained speed of 14 to 18 knots. The blackfish are able to maintain speeds of about 22 knots, and one killer whale seemed able to swim somewhat faster. This implies that the apparent coefficient of surface friction remains approximately constant for dolphins from 6 to 22 ft long, as is the case for rigid bodies.

  20. The development of swimming power

    PubMed Central

    Gatta, Giorgio; Leban, Bruno; Paderi, Maurizio; Padulo, Johnny; Migliaccio, Gian Mario; Pau, Massimiliano

    2014-01-01

    Summary Purpose: the aim of this study was to investigate the effects of the transfer strength training method on swimming power. Methods: twenty male swimmers “master“ were randomly allocated to strength (n= 10, ST) and swimming training (n=10, SW) groups. Both groups performed six-weeks training based on swimming training for SW and strength training which consisted in a weight training session immediately followed by the maximum swimming velocity. The performance in both groups was assessed by Maximal-Mechanical-External-Power (MMEP) before and after the six-weeks period, using a custom ergometer that provided force, velocity, and power measurement in water. Results: a significant increased MMEP in ST group (5.73% with p< 0.05) was obtained by an increased strength (11.70% with p< 0.05) and a decreased velocity (4.99% with p> 0.05). Conversely, in the SW group there was a decreased in MMEP (7.31%; p< 0.05), force and velocity (4.16%, and 3.45; respectively p> 0.05). Conclusion: this study showed that the transfer training method, based on combination of weight training (in dry condition) immediately followed by fast swim (in water) significantly improves swimming-power in master. PMID:25767781

  1. Unsteady turbulent boundary layers in swimming rainbow trout.

    PubMed

    Yanase, Kazutaka; Saarenrinne, Pentti

    2015-05-01

    The boundary layers of rainbow trout, Oncorhynchus mykiss, swimming at 1.02±0.09 L s(-1) (mean±s.d., N=4), were measured by the particle image velocimetry (PIV) technique at a Reynolds number of 4×10(5). The boundary layer profile showed unsteadiness, oscillating above and beneath the classical logarithmic law of the wall with body motion. Across the entire surface regions that were measured, local Reynolds numbers based on momentum thickness, which is the distance that is perpendicular to the fish surface through which the boundary layer momentum flows at free-stream velocity, were greater than the critical value of 320 for the laminar-to-turbulent transition. The skin friction was dampened on the convex surface while the surface was moving towards a free-stream flow and increased on the concave surface while retreating. These observations contradict the result of a previous study using different species swimming by different methods. Boundary layer compression accompanied by an increase in local skin friction was not observed. Thus, the overall results may not support absolutely the Bone-Lighthill boundary layer thinning hypothesis that the undulatory motions of swimming fish cause a large increase in their friction drag because of the compression of the boundary layer. In some cases, marginal flow separation occurred on the convex surface in the relatively anterior surface region, but the separated flow reattached to the fish surface immediately downstream. Therefore, we believe that a severe impact due to induced drag components (i.e. pressure drag) on the swimming performance, an inevitable consequence of flow separation, was avoided.

  2. Is paramecium swimming autonomic?

    NASA Astrophysics Data System (ADS)

    Bandyopadhyay, Promode R.; Toplosky, Norman; Hansen, Joshua

    2010-11-01

    We seek to explore if the swimming of paramecium has an underlying autonomic mechanism. Such robotic elements may be useful in capturing the disturbance field in an environment in real time. Experimental evidence is emerging that motion control neurons of other animals may be present in paramecium as well. The limit cycle determined using analog simulation of the coupled nonlinear oscillators of olivo-cerebellar dynamics (ieee joe 33, 563-578, 2008) agrees with the tracks of the cilium of a biological paramecium. A 4-motor apparatus has been built that reproduces the kinematics of the cilium motion. The motion of the biological cilium has been analyzed and compared with the results of the finite element modeling of forces on a cilium. The modeling equates applied torque at the base of the cilium with drag, the cilium stiffness being phase dependent. A low friction pendulum apparatus with a multiplicity of electromagnetic actuators is being built for verifying the maps of the attractor basin computed using the olivo-cerebellar dynamics for different initial conditions. Sponsored by ONR 33.

  3. Swimming in Sculptor

    NASA Image and Video Library

    2016-03-07

    Peering deep into the early Universe, this picturesque parallel field observation from the NASA/ESA Hubble Space Telescope reveals thousands of colourful galaxies swimming in the inky blackness of space. A few foreground stars from our own galaxy, the Milky Way, are also visible. In October 2013 Hubble’s Wide Field Camera 3 (WFC3) and Advanced Camera for Surveys (ACS) began observing this portion of sky as part of the Frontier Fields programme. This spectacular skyscape was captured during the study of the giant galaxy cluster Abell 2744, otherwise known as Pandora’s Box. While one of Hubble’s cameras concentrated on Abell 2744, the other camera viewed this adjacent patch of sky near to the cluster. Containing countless galaxies of various ages, shapes and sizes, this parallel field observation is nearly as deep as the Hubble Ultra-Deep Field. In addition to showcasing the stunning beauty of the deep Universe in incredible detail, this parallel field — when compared to other deep fields — will help astronomers understand how similar the Universe looks in different directions

  4. Hydrodynamics and energy-saving swimming techniques of Pacific bluefin tuna.

    PubMed

    Takagi, Tsutomu; Tamura, Yumiko; Weihs, Daniel

    2013-11-07

    Weihs theoretically revealed that during the movement of fish with negative buoyancy, more kinetic energy is saved in the glide and upward (GAU) swimming mode than in the continuous horizontal swimming mode. Because kinetic energy saving depends on dynamic parameters such as the drag and lift of the body, the effects of variations in these parameters on energy saving for different species remain unknown. Here, the kinetic energy saving of Pacific bluefin tuna (PBT), Thunnus orientalis, exhibiting the GAU swimming mode was investigated. The dynamic properties of PBT were estimated by carrying out CFD analysis. The CFD model was produced by using a three-dimensional laser surface profiler, and the model was controlled such that it exhibited swimming motion similar to that of a live PBT swimming in a flume tank. The drag generated by tail beating, which significantly affects the kinetic energy during motion, was twice that generated in the glide mode. The faster the upward swimming speed, the lesser is the kinetic energy saving; therefore, when the upward swimming speed is more than twice the glide speed, there is no gain in the GAU mode. However, when SMR (Standard Metabolic Rate) is considered, if the energy based on SMR is assumed to be 30% of the total energy spent during motion, the most efficient upward swimming speed is 1.4 times the glide speed. The GAU swimming mode of PBT leads to energy saving during motion, and the upward swimming speed and the lift force produced by the pectoral fins for the most efficient drive are unique for different species of different sizes.

  5. Bobcat Walking and Swimming

    NASA Image and Video Library

    2014-03-06

    CAPE CANAVERAL, Fla. – A bobcat walks on the shore of a canal near the NASA News Center at Kennedy Space Center in Florida. The center shares a boundary with the Merritt Island National Wildlife Refuge. The refuge encompasses 140,000 acres that are a habitat for more than 330 species of birds, 31 mammals, 117 fishes, and 65 amphibians and reptiles. Photo credit: NASA/Daniel Casper

  6. Bobcat Walking and Swimming

    NASA Image and Video Library

    2014-03-06

    CAPE CANAVERAL, Fla. – A bobcat walks along a canal near the NASA News Center at Kennedy Space Center in Florida. The center shares a boundary with the Merritt Island National Wildlife Refuge. The refuge encompasses 140,000 acres that are a habitat for more than 330 species of birds, 31 mammals, 117 fishes, and 65 amphibians and reptiles. Photo credit: NASA/Daniel Casper

  7. Bobcat Walking and Swimming

    NASA Image and Video Library

    2014-03-06

    CAPE CANAVERAL, Fla. – A bobcat walks along a canal near the NASA News Center at Kennedy Space Center in Florida. The center shares a boundary with the Merritt Island National Wildlife Refuge. The refuge encompasses 140,000 acres that are a habitat for more than 330 species of birds, 31 mammals, 117 fishes, and 65 amphibians and reptiles. Photo credit: NASA/Daniel Casper. Note: Selected image is cropped

  8. Bobcat Walking and Swimming

    NASA Image and Video Library

    2014-03-06

    CAPE CANAVERAL, Fla. – A bobcat pauses to look back at the photographer while out for a walk at NASA's Kennedy Space Center in Florida. The center shares a boundary with the Merritt Island National Wildlife Refuge. The refuge encompasses 140,000 acres that are a habitat for more than 330 species of birds, 31 mammals, 117 fishes, and 65 amphibians and reptiles. Photo credit: NASA/Daniel Casper Note: selected image is cropped

  9. Colonization of abandoned swimming pools by larval mosquitoes and their predators following Hurricane Katrina.

    PubMed

    Caillouët, Kevin A; Carlson, John C; Wesson, Dawn; Jordan, Frank

    2008-06-01

    Thousands of flooded swimming pools were abandoned in New Orleans following Hurricane Katrina and provided a natural experiment to examine colonization of a novel aquatic habitat by mosquito larvae and their aquatic predators. We conducted a randomized survey of flooded swimming pools in two neighborhoods in January 2006 and found that 64% contained mosquito larvae, 92% contained predatory invertebrates, and 47% contained fishes. We collected 12,379 immature mosquitoes representing five species, primarily Culiseta inornata, and secondarily, the arboviral vector Culex quinquefasciatus. Dragonfly nymphs in the families Aeshnidae and Libellulidae were the most common predatory invertebrates collected among a total of 32 non-mosquito invertebrate species. Eleven species of fishes were collected, with Gambusia affinis accounting for 76% of the catch. Diversity of fishes in swimming pools was positively correlated with proximity to a levee breach and the fish assemblage found in swimming pools was similar to that found along shorelines of Lake Pontchartrain and drainage canals that flooded the study area. Mosquito larvae were rare or absent from pools containing fishes; however, path analysis indicated that the presence of top predators or abundant competitors may somewhat mitigate the effect of Gambusia affinis on mosquito presence.

  10. The undulatory swimming gait of elongated swimmers revisited.

    PubMed

    Iosilevskii, Gil

    2017-03-31

    An undulatory swimming gait is characterized by short lateral displacement waves that propagate backwards along the body of the swimmer faster than it swims. Hydrodynamic theory of elongated bodies predicts that if the amplitude of the displacement waves does not increase toward the caudal end, the part of the swimmer posteriad of the dorso-ventrally widest point takes no part in propulsion. It also predicts that if the amplitude does increase, then the hydrodynamic propulsion efficiency suffers. Cusk eels have their widest point located in the anterior half of the body with the bulk of their locomotive muscles located posteriad of it; indeed, they swim so that the amplitude of the propulsion wave increases toward the caudal end. Anguillid eels have their widest point posteriad of the mid-body, and their locomotive muscles are distributed along their entire length-but they swim as cusk eels, using the posterior half only. Apparently, both use hydrodynamically inefficient gaits. The paper questions the definition of propulsion efficiency and shows that biomechanical considerations are more important than hydrodynamic, and that most probably fish adjust their gait to maximize the ratio between the energy made good (the product of thrust and distance) and the chemical energy consumed by the muscles. The role of body shape is discussed.

  11. Ammonia toxicity in fish.

    PubMed

    Randall, D J; Tsui, T K N

    2002-01-01

    Ammonia is present in the aquatic environment due to agricultural run-off and decomposition of biological waste. Ammonia is toxic to all vertebrates causing convulsions, coma and death, probably because elevated NH4+ displaces K+ and depolarizes neurons, causing activation of NMDA type glutamate receptor, which leads to an influx of excessive Ca2+ and subsequent cell death in the central nervous system. Present ammonia criteria for aquatic systems are based on toxicity tests carried out on, starved, resting, non-stressed fish. This is doubly inappropriate. During exhaustive exercise and stress, fish increase ammonia production and are more sensitive to external ammonia. Present criteria do not protect swimming fish. Fish have strategies to protect them from the ammonia pulse following feeding, and this also protects them from increases in external ammonia, as a result starved fish are more sensitive to external ammonia than fed fish. There are a number of fish species that can tolerate high environmental ammonia. Glutamine formation is an important ammonia detoxification strategy in the brain of fish, especially after feeding. Detoxification of ammonia to urea has also been observed in elasmobranches and some teleosts. Reduction in the rate of proteolysis and the rate of amino acid catabolism, which results in a decrease in ammonia production, may be another strategy to reduce ammonia toxicity. The weather loach volatilizes NH3, and the mudskipper, P. schlosseri, utilizes yet another unique strategy, it actively pumps NH4+ out of the body.

  12. Computational hydrodynamics of animal swimming: boundary element method and three-dimensional vortex wake structure.

    PubMed

    Cheng, J Y; Chahine, G L

    2001-12-01

    The slender body theory, lifting surface theories, and more recently panel methods and Navier-Stokes solvers have been used to study the hydrodynamics of fish swimming. This paper presents progress on swimming hydrodynamics using a boundary integral equation method (or boundary element method) based on potential flow model. The unsteady three-dimensional BEM code 3DynaFS that we developed and used is able to model realistic body geometries, arbitrary movements, and resulting wake evolution. Pressure distribution over the body surface, vorticity in the wake, and the velocity field around the body can be computed. The structure and dynamic behavior of the vortex wakes generated by the swimming body are responsible for the underlying fluid dynamic mechanisms to realize the high-efficiency propulsion and high-agility maneuvering. Three-dimensional vortex wake structures are not well known, although two-dimensional structures termed 'reverse Karman Vortex Street' have been observed and studied. In this paper, simulations about a swimming saithe (Pollachius virens) using our BEM code have demonstrated that undulatory swimming reduces three-dimensional effects due to substantially weakened tail tip vortex, resulting in a reverse Karman Vortex Street as the major flow pattern in the three-dimensional wake of an undulating swimming fish.

  13. Effect of Erabu sea snake (Laticauda semifasciata) lipids on the swimming endurance of mice.

    PubMed

    Zhang, Guihua; Higuchi, Tomoyuki; Shirai, Nobuya; Suzuki, Hiramitsu; Shimizu, Eiji

    2007-01-01

    This study was designed to investigate the effect of Erabu sea snake (Laticauda semifasciata) lipids on the swimming endurance of mice. Twelve-week-old male Crlj: CD-1 (ICR) mice were fed one of three experimental diets containing 6% lard, fish oil or sea snake lipids for 16 weeks. Swimming exercise was conducted in an acrylic plastic tank filled with 25 cm of water maintained at 23 degrees C. Every 4 weeks, the mice were made to perform swimming exercises with loads attached to their tails, corresponding to approximately 1 or 2% of their body weights. The group fed the sea snake lipid diet exhibited significantly improved swimming endurance compared with the lard diet group (p < 0.05); however, this result was not observed in the fish oil diet group. In the sea snake lipid diet group, plasma and muscle lactates were significantly lower, and plasma glucose and muscle glycogen were significantly higher than in the lard diet group (p < 0.05). These results suggest that the intake of sea snake lipids enhanced the swimming endurance of the mice by delaying the accumulation of lactate during swimming exercise. Copyright 2007 S. Karger AG, Basel.

  14. Aerobic swimming performance of juvenile largemouth bronze gudgeon (Coreius guichenoti) in the Yangtze River.

    PubMed

    Tu, Zhiying; Li, Liping; Yuan, Xi; Huang, Yingping; Johnson, David

    2012-06-01

    Largemouth bronze gudgeon (Coreius guichenoti), a fish species once abundant in the Yangtze River, has been rapidly declining in recent years. One important factor, among many, is the interruption of the free-flowing rivers by dams. To obtain data that can be applied to the design of an effective fishway for C. guichenoti and other species in the fish community, a laboratory study of juvenile C. guichenoti's swimming ability and energetics was conducted in a flume-type respirometer equipped with a high-speed video camera system to record swimming behavior. The critical swimming speed (Ucrit ), standard metabolic rate (SMR), and maximum metabolic rate (MO2,max ) were determined during steady swimming at four water temperatures (10, 15, 20, and 25°C). A power function accurately describes the relationship between oxygen consumption rate (MO2 ) and swimming speed (U) at the four temperatures. The Ucrit , SMR, MO2,max , and metabolic scope increased with increasing temperature. The relationship between cost of transport (COT) and U was characteristically inverse bell-shaped, with minimum COT at Uopt = 4.5-5.0 body lengths per second (bl sec(-1)). This investigation provides data on the swimming ability of C. guichenoti that will add to the basic science required for fishway design. © 2012 WILEY PERIODICALS, INC.

  15. Effects of fluoxetine on the swimming and behavioural responses of the Arabian killifish.

    PubMed

    Barry, Michael J

    2013-03-01

    The selective serotonin reuptake inhibitor fluoxetine has frequently been detected in surface waters around the world. Fluoxetine modulates levels of serotonin, a neurotransmitter that regulates several important physiological and behavioural processes including fear and anxiety, aggression, locomotion and feeding. In this study, groups of sub-adult Arabian killifish (Aphanius dispar) were exposed to either 0, 0.03, 0.3 or 3 μg/L fluoxetine hydrochloride for 7 days and their swimming behaviour and social interactions videotaped in a circular arena. The fish were subsequently exposed to a predator alarm chemical (from dragonfly larvae fed with A. dispar) and their short-term responses recorded. The video was analysed using the open-sourced software program Ctrax which objectively quantified swimming and social behaviours. Aggression (chasing behaviour was significantly reduced at 3.0 μg/L fluoxetine. After the addition of the predator alarm chemicals fish responded quickly, increasing the percentage of time spent drifting or motionless and reducing average swimming velocity. Controls and fish exposed to 0.03 or 3 μg/L fluoxetine reduced swimming speed by 20-30 % but returned to pre-exposure velocities within 6 min. Fish exposed to 0.3 μg/L fluoxetine reduced swimming speed by 38 % after addition of the predator alarm and did not return to pre-exposure speeds during the recording period (19 min). Schooling behaviour was also affected by fluoxetine and predator alarm with fish exposed to 0.3 μg/L fluoxetine significantly reducing nearest neighbour distance and swimming speed relative to nearest neighbour the following addition of the predator alarm.

  16. Effect of Erabu sea snake (Laticauda semifasciata) lipids on the swimming endurance of aged mice.

    PubMed

    Zhang, Guihua; Shirai, Nobuya; Higuchi, Tomoyuki; Suzuki, Hiramitsu; Shimizu, Eiji

    2007-12-01

    The effect of Erabu sea snake (Laticauda semifasciata) lipids on the swimming endurance was investigated in aged mice. Fifty three-week-old male Crlj:CD-1 (ICR) mice were fed one of three experimental diets containing either 6% lard, 6% fish oil, or 6% sea snake lipids for 16 wk. The swimming exercise was carried out in an acrylic plastic tank filled with 25 cm of water maintained at 23(o)C. Swimming times to exhaustion were measured with a load of 2% of their body weights attached to the tails of the mice. The swimming times to exhaustion of the group that were fed the sea snake lipid diet tended to be longer than those of the lard diet group, and were significantly improved compared with the fish oil diet group (p<0.05). The plasma and muscle lactate levels were significantly lower in the sea snake lipid diet group than in the lard and fish oil diet groups (p<0.05). The liver glycogen and plasma glucose levels of the sea snake lipid diet group did not differ markedly from those of the lard diet group (p>0.05), and were significantly higher than those of the fish oil diet group (p<0.05). These results suggest that an intake of sea snake lipids but not the fish oil, which is also rich in n-3 polyunsaturated fatty acids (n-3 PUFAs), is useful for improving the swimming endurance of aged mice by attenuating lactate production and/or enhancing lactate clearance during swimming exercise, and the n-3 PUFAs contained in the sea snake lipids did little or nothing for this improved endurance.

  17. Influence of robotic shoal size, configuration, and activity on zebrafish behavior in a free-swimming environment.

    PubMed

    Butail, Sachit; Polverino, Giovanni; Phamduy, Paul; Del Sette, Fausto; Porfiri, Maurizio

    2014-12-15

    In animal studies, robots have been recently used as a valid tool for testing a wide spectrum of hypotheses. These robots often exploit visual or auditory cues to modulate animal behavior. The propensity of zebrafish, a model organism in biological studies, toward fish with similar color patterns and shape has been leveraged to design biologically inspired robots that successfully attract zebrafish in preference tests. With an aim of extending the application of such robots to field studies, here, we investigate the response of zebrafish to multiple robotic fish swimming at different speeds and in varying arrangements. A soft real-time multi-target tracking and control system remotely steers the robots in circular trajectories during the experimental trials. Our findings indicate a complex behavioral response of zebrafish to biologically inspired robots. More robots produce a significant change in salient measures of stress, with a fast robot swimming alone causing more freezing and erratic activity than two robots swimming slowly together. In addition, fish spend more time in the proximity of a robot when they swim far apart than when the robots swim close to each other. Increase in the number of robots also significantly alters the degree of alignment of fish motion with a robot. Results from this study are expected to advance our understanding of robot perception by live animals and aid in hypothesis-driven studies in unconstrained free-swimming environments.

  18. Dynamics of the vortex wakes of flying and swimming vertebrates.

    PubMed

    Rayner, J M

    1995-01-01

    The vortex wakes of flying and swimming animals provide evidence of the history of aero- and hydrodynamic force generation during the locomotor cycle. Vortex-induced momentum flux in the wake is the reaction of forces the animal imposes on its environment, which must be in equilibrium with inertial and external forces. In flying birds and bats, the flapping wings generate lift both to provide thrust and to support the weight. Distinct wingbeat and wake movement patterns can be identified as gaits. In flow visualization experiments, only two wake patterns have been identified: a vortex ring gait with inactive upstroke, and a continuous vortex gait with active upstroke. These gaits may be modelled theoretically by free vortex and lifting line theory to predict mechanical energy consumption, aerodynamic forces and muscle activity. Longer-winged birds undergo a distinct gait change with speed, but shorter-winged species use the vortex ring gait at all speeds. In swimming fish, the situation is more complex: the wake vortices form a reversed von Kármán vortex street, but little is known about the mechanism of generation of the wake, or about how it varies with speed and acceleration or with body form and swimming mode. An unresolved complicating factor is the interaction between the drag wake of the flapping fish body and the thrusting wake from the tail.

  19. Quantitative flow analysis of swimming dynamics with coherent Lagrangian vortices.

    PubMed

    Huhn, F; van Rees, W M; Gazzola, M; Rossinelli, D; Haller, G; Koumoutsakos, P

    2015-08-01

    Undulatory swimmers flex their bodies to displace water, and in turn, the flow feeds back into the dynamics of the swimmer. At moderate Reynolds number, the resulting flow structures are characterized by unsteady separation and alternating vortices in the wake. We use the flow field from simulations of a two-dimensional, incompressible viscous flow of an undulatory, self-propelled swimmer and detect the coherent Lagrangian vortices in the wake to dissect the driving momentum transfer mechanisms. The detected material vortex boundary encloses a Lagrangian control volume that serves to track back the vortex fluid and record its circulation and momentum history. We consider two swimming modes: the C-start escape and steady anguilliform swimming. The backward advection of the coherent Lagrangian vortices elucidates the geometry of the vorticity field and allows for monitoring the gain and decay of circulation and momentum transfer in the flow field. For steady swimming, momentum oscillations of the fish can largely be attributed to the momentum exchange with the vortex fluid. For the C-start, an additionally defined jet fluid region turns out to balance the high momentum change of the fish during the rapid start.

  20. Quantitative flow analysis of swimming dynamics with coherent Lagrangian vortices

    NASA Astrophysics Data System (ADS)

    Huhn, F.; van Rees, W. M.; Gazzola, M.; Rossinelli, D.; Haller, G.; Koumoutsakos, P.

    2015-08-01

    Undulatory swimmers flex their bodies to displace water, and in turn, the flow feeds back into the dynamics of the swimmer. At moderate Reynolds number, the resulting flow structures are characterized by unsteady separation and alternating vortices in the wake. We use the flow field from simulations of a two-dimensional, incompressible viscous flow of an undulatory, self-propelled swimmer and detect the coherent Lagrangian vortices in the wake to dissect the driving momentum transfer mechanisms. The detected material vortex boundary encloses a Lagrangian control volume that serves to track back the vortex fluid and record its circulation and momentum history. We consider two swimming modes: the C-start escape and steady anguilliform swimming. The backward advection of the coherent Lagrangian vortices elucidates the geometry of the vorticity field and allows for monitoring the gain and decay of circulation and momentum transfer in the flow field. For steady swimming, momentum oscillations of the fish can largely be attributed to the momentum exchange with the vortex fluid. For the C-start, an additionally defined jet fluid region turns out to balance the high momentum change of the fish during the rapid start.

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

    PubMed Central

    Tytell, Eric D.; Hsu, Chia-Yu; Williams, Thelma L.; Cohen, Avis H.; Fauci, Lisa J.

    2010-01-01

    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. PMID:21037110

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

    PubMed

    Tytell, Eric D; Hsu, Chia-Yu; Williams, Thelma L; Cohen, Avis H; Fauci, Lisa J

    2010-11-16

    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.

  3. Nutrition for swimming.

    PubMed

    Shaw, Gregory; Boyd, Kevin T; Burke, Louise M; Koivisto, Anu

    2014-08-01

    Swimming is a sport that requires considerable training commitment to reach individual performance goals. Nutrition requirements are specific to the macrocycle, microcycle, and individual session. Swimmers should ensure suitable energy availability to support training while maintaining long term health. Carbohydrate intake, both over the day and in relation to a workout, should be manipulated (3-10 g/kg of body mass/day) according to the fuel demands of training and the varying importance of undertaking these sessions with high carbohydrate availability. Swimmers should aim to consume 0.3 g of high-biological-value protein per kilogram of body mass immediately after key sessions and at regular intervals throughout the day to promote tissue adaptation. A mixed diet consisting of a variety of nutrient-dense food choices should be sufficient to meet the micronutrient requirements of most swimmers. Specific dietary supplements may prove beneficial to swimmers in unique situations, but should be tried only with the support of trained professionals. All swimmers, particularly adolescent and youth swimmers, are encouraged to focus on a well-planned diet to maximize training performance, which ensures sufficient energy availability especially during periods of growth and development. Swimmers are encouraged to avoid rapid weight fluctuations; rather, optimal body composition should be achieved over longer periods by modest dietary modifications that improve their food choices. During periods of reduced energy expenditure (taper, injury, off season) swimmers are encouraged to match energy intake to requirement. Swimmers undertaking demanding competition programs should ensure suitable recovery practices are used to maintain adequate glycogen stores over the entirety of the competition period.

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

    PubMed

    Green, Matthew H; Ho, Robert K; Hale, Melina E

    2011-09-15

    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.

  5. Hydrodynamic interaction of swimming organisms in an inertial regime

    NASA Astrophysics Data System (ADS)

    Li, Gaojin; Ostace, Anca; Ardekani, Arezoo M.

    2016-11-01

    We numerically investigate the hydrodynamic interaction of swimming organisms at small to intermediate Reynolds number regimes, i.e., Re˜O (0.1 -100 ) , where inertial effects are important. The hydrodynamic interaction of swimming organisms in this regime is significantly different from the Stokes regime for microorganisms, as well as the high Reynolds number flows for fish and birds, which involves strong flow separation and detached vortex structures. Using an archetypal swimmer model, called a "squirmer," we find that the inertial effects change the contact time and dispersion dynamics of a pair of pusher swimmers, and trigger hydrodynamic attraction for two pullers. These results are potentially important in investigating predator-prey interactions, sexual reproduction, and the encounter rate of marine organisms such as copepods, ctenophora, and larvae.

  6. Hydrodynamic interaction of swimming organisms in an inertial regime.

    PubMed

    Li, Gaojin; Ostace, Anca; Ardekani, Arezoo M

    2016-11-01

    We numerically investigate the hydrodynamic interaction of swimming organisms at small to intermediate Reynolds number regimes, i.e., Re∼O(0.1-100), where inertial effects are important. The hydrodynamic interaction of swimming organisms in this regime is significantly different from the Stokes regime for microorganisms, as well as the high Reynolds number flows for fish and birds, which involves strong flow separation and detached vortex structures. Using an archetypal swimmer model, called a "squirmer," we find that the inertial effects change the contact time and dispersion dynamics of a pair of pusher swimmers, and trigger hydrodynamic attraction for two pullers. These results are potentially important in investigating predator-prey interactions, sexual reproduction, and the encounter rate of marine organisms such as copepods, ctenophora, and larvae.

  7. Feeding and swimming of flagellates

    NASA Astrophysics Data System (ADS)

    Doelger, Julia; Nielsen, Lasse Tor; Kiorboe, Thomas; Bohr, Tomas; Andersen, Anders

    2015-11-01

    Hydrodynamics plays a dominant role for small planktonic flagellates and shapes their survival strategies. The high diversity of beat patterns and arrangements of appendages indicates different strategies balancing the trade-offs between the general goals, i.e., energy-efficient swimming, feeding, and predator avoidance. One type of flagellated algae that we observe, are haptophytes, which possess two flagella for flow creation and one so-called haptonema, a long, rigid structure fixed on the cell body, which is used for prey capture. We present videos and flow fields obtained using velocimetry methods around freely swimming haptophytes and other flagellates, which we compare to analytical results obtained from point force models. The observed and modelled flows are used to analyse how different morphologies and beat patterns relate to different feeding or swimming strategies, such as the capture mechanism in haptophytes. The Centre for Ocean Life is a VKR center of excellence supported by the Villum foundation.

  8. Paramecium swimming in capillary tube

    NASA Astrophysics Data System (ADS)

    Jana, Saikat; Um, Soong Ho; Jung, Sunghwan

    2012-04-01

    Swimming organisms in their natural habitat need to navigate through a wide range of geometries and chemical environments. Interaction with boundaries in such situations is ubiquitous and can significantly modify the swimming characteristics of the organism when compared to ideal laboratory conditions. We study the different patterns of ciliary locomotion in glass capillaries of varying diameter and characterize the effect of the solid boundaries on the velocities of the organism. Experimental observations show that Paramecium executes helical trajectories that slowly transition to straight lines as the diameter of the capillary tubes decreases. We predict the swimming velocity in capillaries by modeling the system as a confined cylinder propagating longitudinal metachronal waves that create a finite pressure gradient. Comparing with experiments, we find that such pressure gradient considerations are necessary for modeling finite sized ciliary organisms in restrictive geometries.

  9. The Mouse Forced Swim Test

    PubMed Central

    Can, Adem; Dao, David T.; Arad, Michal; Terrillion, Chantelle E.; Piantadosi, Sean C.; Gould, Todd D.

    2012-01-01

    The forced swim test is a rodent behavioral test used for evaluation of antidepressant drugs, antidepressant efficacy of new compounds, and experimental manipulations that are aimed at rendering or preventing depressive-like states. Mice are placed in an inescapable transparent tank that is filled with water and their escape related mobility behavior is measured. The forced swim test is straightforward to conduct reliably and it requires minimal specialized equipment. Successful implementation of the forced swim test requires adherence to certain procedural details and minimization of unwarranted stress to the mice. In the protocol description and the accompanying video, we explain how to conduct the mouse version of this test with emphasis on potential pitfalls that may be detrimental to interpretation of results and how to avoid them. Additionally, we explain how the behaviors manifested in the test are assessed. PMID:22314943

  10. Optimal swimming of a sheet.

    PubMed

    Montenegro-Johnson, Thomas D; Lauga, Eric

    2014-06-01

    Propulsion at microscopic scales is often achieved through propagating traveling waves along hairlike organelles called flagella. Taylor's two-dimensional swimming sheet model is frequently used to provide insight into problems of flagellar propulsion. We derive numerically the large-amplitude wave form of the two-dimensional swimming sheet that yields optimum hydrodynamic efficiency: the ratio of the squared swimming speed to the rate-of-working of the sheet against the fluid. Using the boundary element method, we show that the optimal wave form is a front-back symmetric regularized cusp that is 25% more efficient than the optimal sine wave. This optimal two-dimensional shape is smooth, qualitatively different from the kinked form of Lighthill's optimal three-dimensional flagellum, not predicted by small-amplitude theory, and different from the smooth circular-arc-like shape of active elastic filaments.

  11. The mouse forced swim test.

    PubMed

    Can, Adem; Dao, David T; Arad, Michal; Terrillion, Chantelle E; Piantadosi, Sean C; Gould, Todd D

    2012-01-29

    The forced swim test is a rodent behavioral test used for evaluation of antidepressant drugs, antidepressant efficacy of new compounds, and experimental manipulations that are aimed at rendering or preventing depressive-like states. Mice are placed in an inescapable transparent tank that is filled with water and their escape related mobility behavior is measured. The forced swim test is straightforward to conduct reliably and it requires minimal specialized equipment. Successful implementation of the forced swim test requires adherence to certain procedural details and minimization of unwarranted stress to the mice. In the protocol description and the accompanying video, we explain how to conduct the mouse version of this test with emphasis on potential pitfalls that may be detrimental to interpretation of results and how to avoid them. Additionally, we explain how the behaviors manifested in the test are assessed.

  12. Vortex re-capturing and kinematics in human underwater undulatory swimming.

    PubMed

    Hochstein, Stefan; Blickhan, Reinhard

    2011-10-01

    To maximize swimming speed athletes copy fish undulatory swimming during the underwater period after start and turn. The anatomical limitations may lead to deviations and may enforce compensating strategies. This has been investigated by analyzing the kinematics of two national female swimmers while swimming in a still water pool. Additionally, the flow around and behind the swimmers was measured with the aid of time-resolved particle image velocimetry (TR-2D-PIV). As compared to fish, the swimmers used undulatory waves characterized by much higher Strouhal numbers but very similar amplitude distributions along the body and Froude efficiencies. Vortices generated in the region of strongly flexing joints are suitable to be used pedally to enhance propulsion (vortex re-capturing). Complementing studies using numerical and technical modeling will help us to probe the efficiency of observed mechanisms and further improvements of the human strategy. Copyright © 2010 Elsevier B.V. All rights reserved.

  13. Amoeboid swimming in a channel

    NASA Astrophysics Data System (ADS)

    Wu, Hao; Farutin, Alexander; Hu, Wei-Fan; Thiébaud, Marine; Rafaï, Salima; Peyla, Philippe; Lai, Ming-Chih; Misbah, Chaouqi

    Several micro-organisms, such as bacteria, algae, or spermatozoa, use flagella or cilia to swim in a fluid, while many other micro-organisms instead use ample shape deformation, described as amoeboid, to propel themselves by either crawling on a substrate or swimming. Many eukaryotic cells were believed to require an underlying substratum to migrate (crawl) by using membrane deformation (like blebbing or generation of lamellipodia) but there is now increasing evidence that a large variety of cells (including those of the immune system) can migrate without the assistance of focal adhesion, allowing them to swim as efficiently as they can crawl. This paper details the analysis of amoeboid swimming in a confined fluid by modeling the swimmer as an inextensible membrane deploying local active forces. The swimmer displays a rich behavior: it may settle into a straight trajectory in the channel or navigate from one wall to the other depending on its confinement. The nature of the swimmer is also found to be affected by confinement: the swimmer can behave, on the average over one swimming cycle, as a pusher at low confinement, and becomes a puller at higher confinement. The swimmer's nature is thus not an intrinsic property. The scaling of the swimmer velocity V with the force amplitude A is analyzed in detail showing that at small enough A, $V\\sim A^2/\\eta^2$, whereas at large enough A, V is independent of the force and is determined solely by the stroke frequency and swimmer size. This finding starkly contrasts with currently known results found from swimming models where motion is based on flagellar or ciliary activity, where $V\\sim A/\\eta$. To conclude, two definitions of efficiency as put forward in the literature are analyzed with distinct outcomes. We find that one type of efficiency has an optimum as a function of confinement while the other does not. Future perspectives are outlined.

  14. Swimming in an Unsteady World

    NASA Astrophysics Data System (ADS)

    Koehl, M. A. R.

    2016-02-01

    When animals swim in marine habitats, the water through which they move is usually flowing. Therefore, an important part of understanding the physics of how animals swim in nature is determining how they interact with the fluctuating turbulent water currents in their environment. The research systems we have been using to address this question are microscopic marine animals swimming in turbulent, wavy water flow over spatially-complex communities of organisms growing on surfaces. Field measurements of water motion were used to design realistic turbulent flow in a laboratory wave-flume over different substrata, particle-image velocimetry was used to measure fine-scale, rapidly-varying water velocity vector fields, and planar laser-induced fluorescence was used to measure concentrations of chemical cues from the substratum. We used individual-based models of small animals swimming in this unsteady flow to determine how their trajectories and contacts with substrata were affected by their locomotion through the water, rotation by local shear, response to odors, and transport by ambient flow. We found that the shears, accelerations, and odor concentrations encountered by small swimmers fluctuate rapidly, with peaks much higher than mean values lasting fractions of a second. We identified ways in which the behavior of small, weak swimmers can bias how they are transported by ambient flow (e.g. sinking during brief encounters with shear or odor enhances settlement onto substrata below, whereas constant swimming enhances contact with surfaces above or beside larvae). Although microscopic organisms swim slowly relative to ambient water flow, their locomotory behavior in response to the rapidly-fluctuating shears and odors they encounter can affect where they are transported by ambient water movement.

  15. The effects of chronic cadmium exposure on repeat swimming performance and anaerobic metabolism in brown trout (Salmo trutta) and lake whitefish (Coregonus clupeaformis).

    PubMed

    Cunningham, Jessie L; McGeer, James C

    2016-04-01

    This study investigates the effect of chronic Cd exposure on the ability to perform repeat swim challenges in brown trout (Salmo trutta) and lake whitefish (Coregonus clupeaformis). Fish were exposed to waterborne Cd (18nM) in moderately hard water (120mgL(-1) CaCO3) for 30 days. This level of exposure has been shown to cause sublethal physiological disruption and acclimation responses but no impairment of sustained swimming capacity (Ucrit) in single swim challenges. Swim trials were done over the course of the exposure and each one consisted of an initial swim to 85% of the Ucrit of control fish, a 30min recovery period and finally a second swim challenge to determine Ucrit. Plasma and tissue samples were collected before and after each of the swim periods. As expected from previous studies, Cd exposure resulted in significant accumulation of Cd in gills, liver and kidney but not in white muscle. Exposure also induced a loss of plasma Ca followed by subsequent recovery (in lake whitefish but not brown trout) with few mortalities (100% survival for lake whitefish and 93% for brown trout). Both control and exposed fish swam to 85% of the single swim Ucrit and no differences in performance were seen. The Ucrit of unexposed controls in the second swim challenges were not different from the single swim Ucrit. However, second swim performance was significantly reduced in Cd exposed fish, particularly after a week of exposure where 31% and 38% reductions were observed for brown trout and lake whitefish respectively. Swimming to 85% Ucrit resulted in metabolic expenditure with little recovery after 30min. Few differences were observed between control and Cd exposed fish with the exception of a reduction in resting white muscle ATP stores of Cd exposed fish after 1 week of exposure. The results show that chronic sublethal Cd exposure results in an impairment of swimming ability in repeat swim challenges but this impairment is generally not related to metabolic processes

  16. Unsteady low-Re swimming

    NASA Astrophysics Data System (ADS)

    Pak, On Shun; Lauga, Eric

    2009-11-01

    In this talk, we focus on unsteady effects relevant to the fluid-based locomotion of micro-organisms. First, we consider transient effects in locomotion arising from the inertia of both the swimmer and the surrounding fluid. We discuss and derive the relevant time scales governing transient effects in low Reynolds number swimming, and illustrate them using the prototypical problem of a 2D swimmer starting from rest. Second, we address geometrical unsteadiness resulting from the finite-size of the swimmer. We solve numerically for the swimming kinematics of active (internally-forced) filaments, as models for eukaryotic flagella, and discuss the resulting unsteadiness of the cell body.

  17. Swimming in an Unsteady World.

    PubMed

    Koehl, M A R; Cooper, T

    2015-10-01

    When animals swim in aquatic habitats, the water through which they move is usually flowing. Therefore, an important part of understanding the physics of how animals swim in nature is determining how they interact with the fluctuating turbulent water currents in their environment. We addressed this issue using microscopic larvae of invertebrates in "fouling communities" growing on docks and ships to ask how swimming affects the transport of larvae between moving water and surfaces from which they disperse and onto which they recruit. Field measurements of the motion of water over fouling communities were used to design realistic turbulent wavy flow in a laboratory wave-flume over early-stage fouling communities. Fine-scale measurements of rapidly-varying water-velocity fields were made using particle-image velocimetry, and of dye-concentration fields (analog for chemical cues from the substratum) were made using planar laser-induced fluorescence. We used individual-based models of larvae that were swimming, passively sinking, passively rising, or were passive and neutrally buoyant to determine how their trajectories were affected by their motion through the water, rotation by local shear, and transport by ambient flow. Swimmers moved up and down in the turbulent flow more than did neutrally buoyant larvae. Although more of the passive sinkers landed on substrata below them, and more passive risers on surfaces above, swimming was the best strategy for landing on surfaces if their location was not predictable (as is true for fouling communities). When larvae moved within 5 mm of surfaces below them, passive sinkers and neutrally-buoyant larvae landed on the substratum, whereas many of the swimmers were carried away, suggesting that settling larvae should stop swimming as they near a surface. Swimming and passively-rising larvae were best at escaping from a surface below them, as precompetent larvae must do to disperse away. Velocities, vorticities, and odor

  18. 43 CFR 423.36 - Swimming.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Swimming. 423.36 Section 423.36 Public Lands: Interior Regulations Relating to Public Lands BUREAU OF RECLAMATION, DEPARTMENT OF THE INTERIOR... Swimming. (a) You may swim, wade, snorkel, scuba dive, raft, or tube at your own risk in Reclamation waters...

  19. 36 CFR 327.5 - Swimming.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 36 Parks, Forests, and Public Property 3 2010-07-01 2010-07-01 false Swimming. 327.5 Section 327.5 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY RULES AND REGULATIONS... Swimming. (a) Swimming, wading, snorkeling or scuba diving at one's own risk is permitted, except at...

  20. Shock treatment: swimming pool contact dermatitis.

    PubMed

    Salvaggio, Heather L; Scheman, Andrew J; Chamlin, Sarah L

    2013-01-01

    Allergic contact dermatitis to potassium peroxymonosulfate, used as a chemical shock treatment for hot tubs and swimming pools, should be in the differential diagnosis for patients presenting with dermatitis triggered by swimming pool or hot tub exposure. We report the first pediatric case of allergic contact dermatitis to potassium peroxymonosulfate after swimming exposure. © 2013 Wiley Periodicals, Inc.

  1. 1968 Listing of Swimming Pool Equipment.

    ERIC Educational Resources Information Center

    National Sanitation Foundation, Ann Arbor, MI. Testing Lab.

    An up-to-date listing of swimming pool equipment including--(1) companies authorized to display the National Sanitation Foundation seal of approval, (2) equipment listed as meeting NSF swimming pool equipment standards relating to diatomite type filters, (3) equipment listed as meeting NSF swimming pool equipment standard relating to sand type…

  2. 36 CFR 327.5 - Swimming.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 36 Parks, Forests, and Public Property 3 2012-07-01 2012-07-01 false Swimming. 327.5 Section 327.5 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY RULES AND REGULATIONS... Swimming. (a) Swimming, wading, snorkeling or scuba diving at one's own risk is permitted, except at...

  3. 36 CFR § 331.10 - Swimming.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 3 2013-07-01 2012-07-01 true Swimming. § 331.10 Section § 331.10 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY REGULATIONS..., KENTUCKY AND INDIANA § 331.10 Swimming. Swimming is prohibited unless authorized in writing by the District...

  4. 36 CFR 331.10 - Swimming.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 36 Parks, Forests, and Public Property 3 2011-07-01 2011-07-01 false Swimming. 331.10 Section 331.10 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY REGULATIONS..., KENTUCKY AND INDIANA § 331.10 Swimming. Swimming is prohibited unless authorized in writing by the District...

  5. 36 CFR § 327.5 - Swimming.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 3 2013-07-01 2012-07-01 true Swimming. § 327.5 Section § 327.5 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY RULES AND... § 327.5 Swimming. (a) Swimming, wading, snorkeling or scuba diving at one's own risk is permitted...

  6. 43 CFR 423.36 - Swimming.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 1 2012-10-01 2011-10-01 true Swimming. 423.36 Section 423.36 Public Lands: Interior Regulations Relating to Public Lands BUREAU OF RECLAMATION, DEPARTMENT OF THE INTERIOR... Swimming. (a) You may swim, wade, snorkel, scuba dive, raft, or tube at your own risk in Reclamation waters...

  7. 43 CFR 423.36 - Swimming.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 1 2013-10-01 2013-10-01 false Swimming. 423.36 Section 423.36 Public Lands: Interior Regulations Relating to Public Lands BUREAU OF RECLAMATION, DEPARTMENT OF THE INTERIOR... Swimming. (a) You may swim, wade, snorkel, scuba dive, raft, or tube at your own risk in Reclamation waters...

  8. 43 CFR 423.36 - Swimming.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false Swimming. 423.36 Section 423.36 Public Lands: Interior Regulations Relating to Public Lands BUREAU OF RECLAMATION, DEPARTMENT OF THE INTERIOR... Swimming. (a) You may swim, wade, snorkel, scuba dive, raft, or tube at your own risk in Reclamation waters...

  9. 36 CFR 331.10 - Swimming.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 36 Parks, Forests, and Public Property 3 2012-07-01 2012-07-01 false Swimming. 331.10 Section 331.10 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY REGULATIONS..., KENTUCKY AND INDIANA § 331.10 Swimming. Swimming is prohibited unless authorized in writing by the District...

  10. 36 CFR 327.5 - Swimming.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 3 2014-07-01 2014-07-01 false Swimming. 327.5 Section 327.5 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY RULES AND REGULATIONS... Swimming. (a) Swimming, wading, snorkeling or scuba diving at one's own risk is permitted, except at...

  11. 43 CFR 423.36 - Swimming.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 1 2014-10-01 2014-10-01 false Swimming. 423.36 Section 423.36 Public Lands: Interior Regulations Relating to Public Lands BUREAU OF RECLAMATION, DEPARTMENT OF THE INTERIOR... Swimming. (a) You may swim, wade, snorkel, scuba dive, raft, or tube at your own risk in Reclamation waters...

  12. 36 CFR 327.5 - Swimming.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 36 Parks, Forests, and Public Property 3 2011-07-01 2011-07-01 false Swimming. 327.5 Section 327.5 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY RULES AND REGULATIONS... Swimming. (a) Swimming, wading, snorkeling or scuba diving at one's own risk is permitted, except at...

  13. 36 CFR 331.10 - Swimming.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 3 2014-07-01 2014-07-01 false Swimming. 331.10 Section 331.10 Parks, Forests, and Public Property CORPS OF ENGINEERS, DEPARTMENT OF THE ARMY REGULATIONS..., KENTUCKY AND INDIANA § 331.10 Swimming. Swimming is prohibited unless authorized in writing by the District...

  14. 1968 Listing of Swimming Pool Equipment.

    ERIC Educational Resources Information Center

    National Sanitation Foundation, Ann Arbor, MI. Testing Lab.

    An up-to-date listing of swimming pool equipment including--(1) companies authorized to display the National Sanitation Foundation seal of approval, (2) equipment listed as meeting NSF swimming pool equipment standards relating to diatomite type filters, (3) equipment listed as meeting NSF swimming pool equipment standard relating to sand type…

  15. The Effect of Swimming Experience on Acquisition and Retention of Swimming-Based Taste Aversion Learning in Rats

    ERIC Educational Resources Information Center

    Masaki, Takahisa; Nakajima, Sadahiko

    2010-01-01

    Swimming endows rats with an aversion to a taste solution consumed before swimming. The present study explored whether the experience of swimming before or after the taste-swimming trials interferes with swimming-based taste aversion learning. Experiment 1 demonstrated that a single preexposure to 20 min of swimming was as effective as four or…

  16. The Effect of Swimming Experience on Acquisition and Retention of Swimming-Based Taste Aversion Learning in Rats

    ERIC Educational Resources Information Center

    Masaki, Takahisa; Nakajima, Sadahiko

    2010-01-01

    Swimming endows rats with an aversion to a taste solution consumed before swimming. The present study explored whether the experience of swimming before or after the taste-swimming trials interferes with swimming-based taste aversion learning. Experiment 1 demonstrated that a single preexposure to 20 min of swimming was as effective as four or…

  17. Impacts of Deepwater Horizon crude oil exposure on adult mahi-mahi (Coryphaena hippurus) swim performance.

    PubMed

    Stieglitz, John D; Mager, Edward M; Hoenig, Ronald H; Benetti, Daniel D; Grosell, Martin

    2016-10-01

    The temporal and geographic attributes of the Deepwater Horizon incident in 2010 likely exposed pelagic game fish species, such as mahi-mahi, to crude oil. Although much of the research assessing the effects of the spill has focused on early life stages of fish, studies examining whole-animal physiological responses of adult marine fish species are lacking. Using swim chamber respirometry, the present study demonstrates that acute exposure to a sublethal concentration of the water accommodated fraction of Deepwater Horizon crude oil results in significant swim performance impacts on young adult mahi-mahi, representing the first report of acute sublethal toxicity on adult pelagic fish in the Gulf of Mexico following the spill. At an exposure concentration of 8.4 ± 0.6 µg L(-1) sum of 50 selected polycyclic aromatic hydrocarbons (PAHs; mean of geometric means ± standard error of the mean), significant decreases in the critical and optimal swimming speeds of 14% and 10%, respectively (p < 0.05), were observed. In addition, a 20% reduction in the maximum metabolic rate and a 29% reduction in aerobic scope resulted from exposure to this level of ΣPAHs. Using environmentally relevant crude oil exposure concentrations and a commercially and ecologically valuable Gulf of Mexico fish species, the present results provide insight into the effects of the Deepwater Horizon oil spill on adult pelagic fish. Environ Toxicol Chem 2016;35:2613-2622. © 2016 SETAC. © 2016 SETAC.

  18. Chronic perchlorate exposure impairs stickleback reproductive behaviour and swimming performance

    PubMed Central

    Bernhardt, Richard R.; von Hippel, Frank A.

    2011-01-01

    Summary We describe behavioural changes in two generations of threespine stickleback (Gasterosteus aculeatus) exposed to environmentally relevant concentrations of perchlorate. The first generation (G0,2002) was exposed as two-year-old adults to perchlorate in experimental groups ranging in concentration from less than the method detection limit (<1.1 ppb) to 18.6 ppm for up to 22 days during their courtship, spawning, egg guarding, and first five days of fry guarding. No differences were noted in the behaviour or reproductive output of these fish that were exposed as adults. However, perchlorate exposure throughout development caused widespread effects in the second generation (G1,2003), which was spawned and raised through sexual maturity in one of four nominal experimental groups (0, 30 and 100 ppm, and a ‘variable’ treatment that progressively increased from <1.1 ppb to approximately 60 ppm perchlorate). Dose-dependent effects were found during the G1,2003’s swimming and behavioural evaluations, including higher mortality rates among treated fish following stressful events. Perchlorate-exposed fish had higher failure rates during swimming trials and failed at lower flow rates than control fish. A number of treated fish exhibited seizures. Progressively fewer males completed benchmark metrics, such as nest building, spawning, nursery formation, or fry production, in a dose-dependent manner. Fewer males from higher treatments courted females, and those that did initiated courtship later and had a reduced behavioural repertoire compared to fish from lower treatments. The lowest observed adverse effect level (LOAEL) for swimming performance, reproductive behaviour, survivorship and recruitment was 30 ppm perchlorate (our lowest G1,2003 treatment), and near complete inhibition of reproductive activity was noted among males raised in 100 ppm perchlorate. A small number of treated G1,2003 females were isolated in aquaria, and some performed reproductive

  19. Streamwise vortices destabilize swimming bluegill sunfish (Lepomis macrochirus).

    PubMed

    Maia, Anabela; Sheltzer, Alex P; Tytell, Eric D

    2015-03-01

    In their natural environment, fish must swim stably through unsteady flows and vortices, including vertical vortices, typically shed by posts in a flow, horizontal cross-flow vortices, often produced by a step or a waterfall in a stream, and streamwise vortices, where the axis of rotation is aligned with the direction of the flow. Streamwise vortices are commonly shed by bluff bodies in streams and by ships' propellers and axial turbines, but we know little about their effects on fish. Here, we describe how bluegill sunfish use more energy and are destabilized more often in flow with strong streamwise vorticity. The vortices were created inside a sealed flow tank by an array of four turbines with similar diameter to the experimental fish. We measured oxygen consumption for seven sunfish swimming at 1.5 body lengths (BL) s(-1) with the turbines rotating at 2 Hz and with the turbines off (control). Simultaneously, we filmed the fish ventrally and recorded the fraction of time spent maneuvering side-to-side and accelerating forward. Separately, we also recorded lateral and ventral video for a combination of swimming speeds (0.5, 1.5 and 2.5 BL s(-1)) and turbine speeds (0, 1, 2 and 3 Hz), immediately after turning the turbines on and 10 min later to test for accommodation. Bluegill sunfish are negatively affected by streamwise vorticity. Spills (loss of heading), maneuvers and accelerations were more frequent when the turbines were on than in the control treatment. These unsteady behaviors, particularly acceleration, correlated with an increase in oxygen consumption in the vortex flow. Bluegill sunfish are generally fast to recover from roll perturbations and do so by moving their pectoral fins. The frequency of spills decreased after the turbines had run for 10 min, but was still markedly higher than in the control, showing that fish partially adapt to streamwise vorticity, but not completely. Coping with streamwise vorticity may be an important energetic

  20. Development of a vortex generator to perturb fish locomotion.

    PubMed

    Seth, Deeksha; Flammang, Brooke E; Lauder, George V; Tangorra, James L

    2017-03-15

    Knowledge about the stiffness of fish fins, and whether stiffness is modulated during swimming, is important for understanding the mechanics of a fin's force production. However, the mechanical properties of fins have not been studied during natural swimming, in part because of a lack of instrumentation. To remedy this, a vortex generator was developed that produces traveling vortices of adjustable strength which can be used to perturb the fins of swimming fish. Experiments were conducted to understand how the generator's settings affected the resulting vortex rings. A variety of vortices (14-32 mm diameter traveling at 371-2155 mm s(-1)) were produced that elicited adequate responses from the fish fins to help us to understand the fin's mechanical properties at various swimming speeds (0-350 mm s(-1)).

  1. Shape Optimization of Swimming Sheets

    SciTech Connect

    Wilkening, J.; Hosoi, A.E.

    2005-03-01

    The swimming behavior of a flexible sheet which moves by propagating deformation waves along its body was first studied by G. I. Taylor in 1951. In addition to being of theoretical interest, this problem serves as a useful model of the locomotion of gastropods and various micro-organisms. Although the mechanics of swimming via wave propagation has been studied extensively, relatively little work has been done to define or describe optimal swimming by this mechanism.We carry out this objective for a sheet that is separated from a rigid substrate by a thin film of viscous Newtonian fluid. Using a lubrication approximation to model the dynamics, we derive the relevant Euler-Lagrange equations to optimize swimming speed and efficiency. The optimization equations are solved numerically using two different schemes: a limited memory BFGS method that uses cubic splines to represent the wave profile, and a multi-shooting Runge-Kutta approach that uses the Levenberg-Marquardt method to vary the parameters of the equations until the constraints are satisfied. The former approach is less efficient but generalizes nicely to the non-lubrication setting. For each optimization problem we obtain a one parameter family of solutions that becomes singular in a self-similar fashion as the parameter approaches a critical value. We explore the validity of the lubrication approximation near this singular limit by monitoring higher order corrections to the zeroth order theory and by comparing the results with finite element solutions of the full Stokes equations.

  2. The hydrodynamics of swimming microorganisms

    NASA Astrophysics Data System (ADS)

    Lauga, Eric; Powers, Thomas R.

    2009-09-01

    Cell motility in viscous fluids is ubiquitous and affects many biological processes, including reproduction, infection and the marine life ecosystem. Here we review the biophysical and mechanical principles of locomotion at the small scales relevant to cell swimming, tens of micrometers and below. At this scale, inertia is unimportant and the Reynolds number is small. Our emphasis is on the simple physical picture and fundamental flow physics phenomena in this regime. We first give a brief overview of the mechanisms for swimming motility, and of the basic properties of flows at low Reynolds number, paying special attention to aspects most relevant for swimming such as resistance matrices for solid bodies, flow singularities and kinematic requirements for net translation. Then we review classical theoretical work on cell motility, in particular early calculations of swimming kinematics with prescribed stroke and the application of resistive force theory and slender-body theory to flagellar locomotion. After examining the physical means by which flagella are actuated, we outline areas of active research, including hydrodynamic interactions, biological locomotion in complex fluids, the design of small-scale artificial swimmers and the optimization of locomotion strategies.

  3. Sports Medicine Meets Synchronized Swimming.

    ERIC Educational Resources Information Center

    Wenz, Betty J.; And Others

    This collection of articles contains information about synchronized swimming. Topics covered include general physiology and cardiovascular conditioning, flexibility exercises, body composition, strength training, nutrition, coach-athlete relationships, coping with competition stress and performance anxiety, and eye care. Chapters are included on…

  4. Hydrodynamics of freely swimming flagellates

    NASA Astrophysics Data System (ADS)

    Dolger, Julia; Nielsen, Lasse Tor; Kiorboe, Thomas; Bohr, Tomas; Andersen, Anders

    2016-11-01

    Flagellates are a diverse group of unicellular organisms forming an important part of the marine ecosystem. The arrangement of flagella around the cell serves as a key trait optimizing and compromising essential functions. With micro-particle image velocimetry we observed time-resolved near-cell flows around freely swimming flagellates, and we developed an analytical model based on the Stokes flow around a solid sphere propelled by a variable number of differently placed, temporally varying point forces, each representing one flagellum. The model allows us to reproduce the observed flow patterns and swimming dynamics, and to extract quantities such as swimming velocities and prey clearance rates as well as flow disturbances revealing the organism to flow-sensing predators. Our results point to optimal flagellar arrangements and beat patterns, and essential trade-offs. For biflagellates with two symmetrically arranged flagella we contrasted two species using undulatory and ciliary beat patterns, respectively, and found breast-stroke type beat patterns with equatorial power strokes to be favorable for fast as well as quiet swimming. The Centre for Ocean Life is a VKR Centre of Excellence supported by the Villum Foundation.

  5. Swimming pool-induced asthma.

    PubMed

    Beretta, S; Vivaldo, T; Morelli, M; Carlucci, P; Zuccotti, G V

    2011-01-01

    A 13-year-old elite swimmer presented with wheezing after indoor swimming training. On the basis of her clinical history and the tests performed, exercise-induced asthma and mold-induced asthma were ruled out and a diagnosis of chlorine-induced asthma was made.

  6. Swimming bacteria in liquid crystal

    NASA Astrophysics Data System (ADS)

    Sokolov, Andrey; Zhou, Shuang; Aranson, Igor; Lavrentovich, Oleg

    2014-03-01

    Dynamics of swimming bacteria can be very complex due to the interaction between the bacteria and the fluid, especially when the suspending fluid is non-Newtonian. Placement of swimming bacteria in lyotropic liquid crystal produces a new class of active materials by combining features of two seemingly incompatible constituents: self-propelled live bacteria and ordered liquid crystals. Here we present fundamentally new phenomena caused by the coupling between direction of bacterial swimming, bacteria-triggered flows and director orientations. Locomotion of bacteria may locally reduce the degree of order in liquid crystal or even trigger nematic-isotropic phase transition. Microscopic flows generated by bacterial flagella disturb director orientation. Emerged birefringence patterns allow direct optical observation and quantitative characterization of flagella dynamics. At high concentration of bacteria we observed the emergence of self-organized periodic texture caused by bacteria swimming. Our work sheds new light on self-organization in hybrid bio-mechanical systems and can lead to valuable biomedical applications. Was supported by the US DOE, Office of Basic Energy Sciences, Division of Materials Science and Engineering, under the Contract No. DE AC02-06CH11357.

  7. Sodium bicarbonate improves swimming performance.

    PubMed

    Lindh, A M; Peyrebrune, M C; Ingham, S A; Bailey, D M; Folland, J P

    2008-06-01

    Sodium bicarbonate ingestion has been shown to improve performance in single-bout, high intensity events, probably due to an increase in buffering capacity, but its influence on single-bout swimming performance has not been investigated. The effects of sodium bicarbonate supplementation on 200 m freestyle swimming performance were investigated in elite male competitors. Following a randomised, double blind counterbalanced design, 9 swimmers completed maximal effort swims on 3 separate occasions: a control trial (C); after ingestion of sodium bicarbonate (SB: NaHCO3 300 mg . kg (-1) body mass); and after ingestion of a placebo (P: CaCO3 200 mg . kg (-1) body mass). The SB and P agents were packed in gelatine capsules and ingested 90 - 60 min prior to each 200 m swim. Mean 200 m performance times were significantly faster for SB than C or P (1 : 52.2 +/- 4.7; 1 : 53.7 +/- 3.8; 1 : 54.0 +/- 3.6 min : ss; p < 0.05). Base excess, pH and blood bicarbonate were all elevated pre-exercise in the SB compared to C and P trials (p < 0.05). Post-200 m blood lactate concentrations were significantly higher following the SB trial compared with P and C (p < 0.05). It was concluded that SB supplementation can improve 200 m freestyle performance time in elite male competitors, most likely by increasing buffering capacity.

  8. Adiabatic swimming in an ideal quantum gas.

    PubMed

    Avron, J E; Gutkin, B; Oaknin, D H

    2006-04-07

    Interference effects are important for swimming of mesoscopic systems that are small relative to the coherence length of the surrounding quantum medium. Swimming is geometric for slow swimmers and the distance covered in each stroke is determined, explicitly, in terms of the on-shell scattering matrix. Remarkably, for a one-dimensional Fermi gas at zero temperature we find that slow swimming is topological: the swimming distance covered in one stroke is quantized in half integer multiples of the Fermi wavelength. In addition, a careful choice of the swimming stroke can eliminate dissipation.

  9. Micro- and nanorobots swimming in heterogeneous liquids.

    PubMed

    Nelson, Bradley J; Peyer, Kathrin E

    2014-09-23

    Essentially all experimental investigations of swimming micro- and nanorobots have focused on swimming in homogeneous Newtonian liquids. In this issue of ACS Nano, Schamel et al. investigate the actuation of "nanopropellers" in a viscoelastic biological gel that illustrates the importance of the size of the nanostructure relative to the gel mesh size. In this Perspective, we shed further light on the swimming performance of larger microrobots swimming in heterogeneous liquids. One of the interesting results of our work is that earlier findings on the swimming performance of motile bacteria in heterogeneous liquids agree, in principle, with our results. We also discuss future research directions that should be pursued in this fascinating interdisciplinary field.

  10. Suspension biomechanics of swimming microbes

    PubMed Central

    Ishikawa, Takuji

    2009-01-01

    Micro-organisms play a vital role in many biological, medical and engineering phenomena. Some recent research efforts have demonstrated the importance of biomechanics in understanding certain aspects of micro-organism behaviours such as locomotion and collective motions of cells. In particular, spatio-temporal coherent structures found in a bacterial suspension have been the focus of many research studies over the last few years. Recent studies have shown that macroscopic properties of a suspension, such as rheology and diffusion, are strongly affected by meso-scale flow structures generated by swimming microbes. Since the meso-scale flow structures are strongly affected by the interactions between microbes, a bottom-up strategy, i.e. from a cellular level to a continuum suspension level, represents the natural approach to the study of a suspension of swimming microbes. In this paper, we first provide a summary of existing biomechanical research on interactions between a pair of swimming micro-organisms, as a two-body interaction is the simplest many-body interaction. We show that interactions between two nearby swimming micro-organisms are described well by existing mathematical models. Then, collective motions formed by a group of swimming micro-organisms are discussed. We show that some collective motions of micro-organisms, such as coherent structures of bacterial suspensions, are satisfactorily explained by fluid dynamics. Lastly, we discuss how macroscopic suspension properties are changed by the microscopic characteristics of the cell suspension. The fundamental knowledge we present will be useful in obtaining a better understanding of the behaviour of micro-organisms. PMID:19674997

  11. Condition, prolonged swimming performance and muscle metabolic capacities of cod Gadus morhua.

    PubMed

    Martínez, M; Guderley, H; Dutil, J-D; Winger, P D; He, P; Walsh, S J

    2003-02-01

    This study evaluated the link between swimming endurance and condition of Atlantic cod Gadus morhua that had been fed or starved during the 16 weeks preceding the tests, and assessed whether muscle metabolic capacities explain such links. The condition factor [(somatic mass x fork length(-3))x100] of starved cod was 0.54+/-0.1 whereas that of fed cod was 0.81+/-0.1. In white and red muscle, we measured four glycolytic enzymes: phosphofructokinase (PFK), pyruvate kinase (PK), creatine kinase (CK) and lactate dehydrogenase (LDH), two mitochondrial enzymes: cytochrome c oxidase (CCO) and citrate synthase (CS), a biosynthetic enzyme, nucleoside diphosphate kinase (NDPK), glycogen and protein levels and water content. Muscle samples were taken at three positions along the length of the fish; starvation affected the metabolic capacities of white muscle more than those of red muscle. The levels of glycolytic enzymes and glycogen changed more in white than red muscle during starvation. Both in fed and starved cod, muscle metabolic capacities varied with position along the fish; starvation reduced this longitudinal variation more in white than red muscle. In white muscle of fed cod, the glycolytic enzyme levels increased from head to tail, while in starved cod this longitudinal variation disappeared. In red muscle mitochondrial enzyme levels were highest in the caudal sample, but fewer differences were found for glycolytic enzymes. Swimming endurance was markedly affected by fish condition, with starved fish swimming only 30% of the time (and distance) of fed fish. This endurance was closely linked with the number of burst-coast movements during the test and the activity of CCO and LDH in white muscle. The number of burst-coast movements was significantly linked with condition factor and PFK activity in caudal red muscle and gill arch mass. Our data indicated that cod use both glycolytic and oxidative capacities to support endurance swimming. Furthermore, swimming endurance

  12. The infrabranchial musculature and its bearing on the phylogeny of percomorph fishes (Osteichthyes: Teleostei).

    PubMed

    Datovo, Aléssio; de Pinna, Mário C C; Johnson, G David

    2014-01-01

    The muscles serving the ventral portion of the gill arches ( = infrabranchial musculature) are poorly known in bony fishes. A comparative analysis of the infrabranchial muscles in the major percomorph lineages reveals a large amount of phylogenetically-relevant information. Characters derived from this anatomical system are identified and discussed in light of current hypotheses of phylogenetic relationships among percomorphs. New evidence supports a sister-group relationship between the Batrachoidiformes and Lophiiformes and between the Callionymoidei and Gobiesocoidei. Investigated data also corroborate the existence of two monophyletic groups, one including the Pristolepididae, Badidae, and Nandidae, and a second clade consisting of all non-amarsipid stromateiforms. New synapomorphies are proposed for the Atherinomorphae, Blenniiformes, Lophiiformes, Scombroidei (including Sphyraenidae), and Gobiiformes. Within the latter order, the Rhyacichthyidae and Odontobutidae are supported as the successive sister families of all remaining gobiiforms. The present analysis further confirms the validity of infrabranchial musculature characters previously proposed to support the grouping of the Mugiliformes with the Atherinomorphae and the monophyly of the Labriformes with the possible inclusion of the Pholidichthyiformes. Interestingly, most hypotheses of relationships supported by the infrabranchial musculature have been advanced by preceding anatomists on the basis of distinct data sources, but were never recovered in recent molecular phylogenies. These conflicts clearly indicate the current unsatisfactory resolution of the higher-level phylogeny of percomorphs.

  13. The Infrabranchial Musculature and Its Bearing on the Phylogeny of Percomorph Fishes (Osteichthyes: Teleostei)

    PubMed Central

    Datovo, Aléssio; de Pinna, Mário C. C.; Johnson, G. David

    2014-01-01

    The muscles serving the ventral portion of the gill arches ( = infrabranchial musculature) are poorly known in bony fishes. A comparative analysis of the infrabranchial muscles in the major percomorph lineages reveals a large amount of phylogenetically-relevant information. Characters derived from this anatomical system are identified and discussed in light of current hypotheses of phylogenetic relationships among percomorphs. New evidence supports a sister-group relationship between the Batrachoidiformes and Lophiiformes and between the Callionymoidei and Gobiesocoidei. Investigated data also corroborate the existence of two monophyletic groups, one including the Pristolepididae, Badidae, and Nandidae, and a second clade consisting of all non-amarsipid stromateiforms. New synapomorphies are proposed for the Atherinomorphae, Blenniiformes, Lophiiformes, Scombroidei (including Sphyraenidae), and Gobiiformes. Within the latter order, the Rhyacichthyidae and Odontobutidae are supported as the successive sister families of all remaining gobiiforms. The present analysis further confirms the validity of infrabranchial musculature characters previously proposed to support the grouping of the Mugiliformes with the Atherinomorphae and the monophyly of the Labriformes with the possible inclusion of the Pholidichthyiformes. Interestingly, most hypotheses of relationships supported by the infrabranchial musculature have been advanced by preceding anatomists on the basis of distinct data sources, but were never recovered in recent molecular phylogenies. These conflicts clearly indicate the current unsatisfactory resolution of the higher-level phylogeny of percomorphs. PMID:25310286

  14. Pre-task music improves swimming performance.

    PubMed

    Smirmaul, B P; Dos Santos, R V; Da Silva Neto, L V

    2015-12-01

    The purpose of this study was to investigate the effects of pre-task music on swimming performance and other psychological variables. A randomized counterbalanced within-subjects (experimental and control condition) design was employed. Eighteen regional level male swimmers performed two 200-m freestyle swimming time trials. Participants were exposed to either 5 minutes of self-selected music (pre-task music condition) or 5 minutes of silence (control condition) and, after 1 minute, performed the swimming task. Swimming time was significantly shorter (-1.44%) in the pre-task music condition. Listening to pre-task music increased motivation to perform the swimming task, while arousal remained unchanged. While fatigue increased after the swimming task in both conditions, vigor, ratings of perceived exertion and affective valence were unaltered. It is concluded, for the first time, that pre-task music improves swimming performance.

  15. Power production during steady swimming in largemouth bass and rainbow trout.

    PubMed

    Coughlin, D J

    2000-02-01

    Steady swimming in fishes is powered by the aerobic or red muscle, but there are conflicting theories on the relative roles of the anterior and posterior red muscle in powering steady swimming. To examine how red muscle is used to power steady swimming in rainbow trout (Oncorhynchus mykiss), electromyographic (EMG) and sonomicrometry recordings were made of muscle activity in vivo. These data were used in in vitro work-loop studies of muscle power production. Data on in vitro power production were also collected for largemouth bass (Micropterus salmoides) red muscle from previously published data on in vivo muscle activity. The in vivo data collected from swimming trout were similar to those for other species. The anterior red muscle of these fish has the longest duty cycle, the smallest phase shift between the onset of EMG activity and maximum muscle length during each tailbeat and undergoes the smallest strain or length change. For both trout and largemouth bass, work-loop experiments indicate that the majority of power for steady swimming is generated by the posterior muscle, as has been observed in other species.

  16. Swimming behavior of the nudibranch Melibe leonina.

    PubMed

    Lawrence, K A; Watson, W H

    2002-10-01

    Swimming in the nudibranch Melibe leonina consists of five types of movements that occur in the following sequence: (1) withdrawal, (2) lateral flattening, (3) a series of lateral flexions, (4) unrolling and swinging, and (5) termination. Melibe swims spontaneously, as well as in response to different types of aversive stimuli. In this study, swimming was elicited by contact with the tube feet of the predatory sea star Pycnopodia helianthoides, pinching with forceps, or application of a 1 M KCl solution. During an episode of swimming, the duration of swim cycles (2.7 +/- 0.2 s [mean +/- SEM], n = 29) and the amplitude of lateral flexions remained relatively constant. However, the latency between the application of a stimulus and initiation of swimming was more variable, as was the duration of an episode of swimming. For example, when touched with a single tube foot from a sea star (n = 32), the latency to swim was 7.0 +/- 2.4 s, and swimming continued for 53.7 +/- 9.4 s, whereas application of KCl resulted in a longer latency to swim (22.3 +/- 4.5 s) and more prolonged swimming episodes (174.9 +/- 32.1 s). Swimming individuals tended to move in a direction perpendicular to the long axis of the foot, which propelled them laterally when they were oriented with the oral hood toward the surface of the water. The results of this study indicate that swimming in Melibe, like that in several other molluscs, is a stereotyped fixed action pattern that can be reliably elicited in the laboratory. These characteristics, along with the large identifiable neurons typical of many molluscs, make swimming in this nudibranch amenable to neuroethological analyses.

  17. Model identification and controller design of a fish-like robot

    NASA Astrophysics Data System (ADS)

    Ariyanto, Irfan; Kang, Taesam; Chan, Wai Leung; Lee, Youngjae

    2007-04-01

    Robotic fish is an interesting and prospective subject to develop. The simplest fish swimming mode to be mimicked for fish robots is the ostraciiform mode which only requires caudal fin flapping. An almost submerged ostraciiform fish robot was constructed to study its swimming characteristics. The swimming direction can be controlled by changing the mean angle of caudal fin oscillation. Experiments were conducted to study the behavior of the fish robot and in particular, the transfer function between swimming path angular rate and mean angle of the caudal fin oscillation were identified. Error to signal ratio quantity was used to determine how well the model fits with the experimental data. This identification model was used to design a 2-degree-of-freedom PID controller that meets some specific requirements to improve the steering performance.

  18. Effects of soft-water acclimation on the physiology, swimming performance, and cardiac parameters of the rainbow trout, Oncorhynchus mykiss.

    PubMed

    Dussault, E B; Playle, R C; Dixon, D G; McKinley, R S

    2008-12-01

    Rainbow trout acclimated to soft water were submitted to an incremental velocity trial, and exhibited a 14% decrease in critical swimming speed (U(crit) * 1.37 +/- 0.055 vs. 1.54 +/- 0.044 m s(-1)) compared to fish kept in hard water. After a standardized swimming protocol, soft-water-acclimated fish had higher blood lactate concentrations (6.5 +/- 0.66 and 6.0 +/- 0.64 mmol L(-1) (soft water) vs. 5.0 +/- 0.46 and 3.9 +/- 0.32 mmol L(-1) (hard water)), revealing a greater use of anaerobic metabolism for the same exercise. Cardiovascular parameters were investigated while fish were swimming at increasing water velocities, revealing that soft-water-acclimated fish had lower increases in heart rate (105% vs. 118% of pre-exercise values), due to higher heart rates observed during acclimation and during the first 10 min of the swimming trial. This was also reflected by the plateau in heart rate and stroke volume observed during the swimming protocol, which can be attributed to increased cardiovascular function in response to soft-water acclimation. These results are in accord with previously reported increases in blood-to-water diffusion distance, due to proliferation of chloride cells at the gills in response to soft-water conditions, and underscore the costs and limitations of soft-water acclimation.

  19. How body torque and Strouhal number change with swimming speed and developmental stage in larval zebrafish.

    PubMed

    van Leeuwen, Johan L; Voesenek, Cees J; Müller, Ulrike K

    2015-09-06

    Small undulatory swimmers such as larval zebrafish experience both inertial and viscous forces, the relative importance of which is indicated by the Reynolds number (Re). Re is proportional to swimming speed (vswim) and body length; faster swimming reduces the relative effect of viscous forces. Compared with adults, larval fish experience relatively high (mainly viscous) drag during cyclic swimming. To enhance thrust to an equally high level, they must employ a high product of tail-beat frequency and (peak-to-peak) amplitude fAtail, resulting in a relatively high fAtail/vswim ratio (Strouhal number, St), and implying relatively high lateral momentum shedding and low propulsive efficiency. Using kinematic and inverse-dynamics analyses, we studied cyclic swimming of larval zebrafish aged 2-5 days post-fertilization (dpf). Larvae at 4-5 dpf reach higher f (95 Hz) and Atail (2.4 mm) than at 2 dpf (80 Hz, 1.8 mm), increasing swimming speed and Re, indicating increasing muscle powers. As Re increases (60 → 1400), St (2.5 → 0.72) decreases nonlinearly towards values of large swimmers (0.2-0.6), indicating increased propulsive efficiency with vswim and age. Swimming at high St is associated with high-amplitude body torques and rotations. Low propulsive efficiencies and large yawing amplitudes are unavoidable physical constraints for small undulatory swimmers. © 2015 The Author(s).

  20. How body torque and Strouhal number change with swimming speed and developmental stage in larval zebrafish

    PubMed Central

    van Leeuwen, Johan L.; Voesenek, Cees J.; Müller, Ulrike K.

    2015-01-01

    Small undulatory swimmers such as larval zebrafish experience both inertial and viscous forces, the relative importance of which is indicated by the Reynolds number (Re). Re is proportional to swimming speed (vswim) and body length; faster swimming reduces the relative effect of viscous forces. Compared with adults, larval fish experience relatively high (mainly viscous) drag during cyclic swimming. To enhance thrust to an equally high level, they must employ a high product of tail-beat frequency and (peak-to-peak) amplitude fAtail, resulting in a relatively high fAtail/vswim ratio (Strouhal number, St), and implying relatively high lateral momentum shedding and low propulsive efficiency. Using kinematic and inverse-dynamics analyses, we studied cyclic swimming of larval zebrafish aged 2–5 days post-fertilization (dpf). Larvae at 4–5 dpf reach higher f (95 Hz) and Atail (2.4 mm) than at 2 dpf (80 Hz, 1.8 mm), increasing swimming speed and Re, indicating increasing muscle powers. As Re increases (60 → 1400), St (2.5 → 0.72) decreases nonlinearly towards values of large swimmers (0.2–0.6), indicating increased propulsive efficiency with vswim and age. Swimming at high St is associated with high-amplitude body torques and rotations. Low propulsive efficiencies and large yawing amplitudes are unavoidable physical constraints for small undulatory swimmers. PMID:26269230

  1. Adaptation and acclimation of traits associated with swimming capacity in Lake Whitefish (coregonus clupeaformis) ecotypes.

    PubMed

    Laporte, Martin; Dalziel, Anne C; Martin, Nicolas; Bernatchez, Louis

    2016-08-11

    Improved performance in a given ecological niche can occur through local adaptation, phenotypic plasticity, or a combination of these mechanisms. Evaluating the relative importance of these two mechanisms is needed to better understand the cause of intra specific polymorphism. In this study, we reared populations of Lake Whitefish (Coregonus clupeaformis) representing the'normal' (benthic form) and the 'dwarf' (derived limnetic form) ecotypes in two different conditions (control and swim-training) to test the relative importance of adaptation and acclimation in the differentiation of traits related to swimming capacity. The dwarf whitefish is a more active swimmer than the normal ecotype, and also has a higher capacity for aerobic energy production in the swimming musculature. We hypothesized that dwarf fish would show changes in morphological and physiological traits consistent with reductions in the energetic costs of swimming and maintenance metabolism. We found differences in traits predicted to decrease the costs of prolonged swimming and standard metabolic rate and allow for a more active lifestyle in dwarf whitefish. Dwarf whitefish evolved a more streamlined body shape, predicted to lead to a decreased drag, and a smaller brain, which may decrease their standard metabolic rate. Contrary to predictions, we also found evidence of acclimation in liver size and metabolic enzyme activities. Results support the view that local adaptation has contributed to the genetically-based divergence of traits associated with swimming activity. Presence of post-zygotic barriers limiting gene flow between these ecotype pairs may have favoured repeated local adaptation to the limnetic niches.

  2. Swimming ability and ecological performance of cultured and wild European sea bass (Dicentrarchus labrax) in coastal tidal ponds.

    PubMed

    Handelsman, Corey; Claireaux, Guy; Nelson, Jay A

    2010-01-01

    Locomotor performance is commonly used to predict ecological performance of animals and is often considered a proxy for Darwinian fitness. In fish, swimming performance is often measured in the laboratory, but its contribution to individual success in the field is rarely evaluated. We assessed maximal swimming velocity of wild and cultured juvenile Dicentrarchus labrax (European sea bass) in a sprint performance chamber and found substantial variation among individuals within a cohort and differences between wild and cultured fish. Moreover, individual sprint swimming performance was found to be repeatable on a daily basis, making this test potentially useful for studies of individual fitness. Some animals were also tested for endurance performance with a modified critical swimming speed (U(crit)) test that we had previously reported to be variable among individuals and significantly repeatable over 6 mo. To test whether these different swimming abilities might contribute to differential ecological success in sea bass, cultured juveniles of known sprint and endurance performance were released into experimental estuaries, where they foraged on natural prey under high densities without predation. A second experiment exposed both cultured and wild juveniles of known sprinting ability to natural forage but this time with reduced densities and natural avian predation. Ecological performance was assessed as survival and growth rate. Neither swimming performance was a direct predictor of ecological performance for cultured fish at high densities. Survival under these conditions was significantly predicted by prior growth rate and condition factor. When exposed to natural avian predators, the better-sprinting wild fish outperformed cultured fish (35% vs. 0% survival), and there was some evidence for sprinting ability contributing to survival within wild fish. Measuring sprint performance in mesocosm survivors revealed a significant inverse relationship between rapid growth

  3. Swimming performance and energetics as a function of temperature in killifish Fundulus heteroclitus.

    PubMed

    Fangue, Nann A; Mandic, Milica; Richards, Jeffrey G; Schulte, Patricia M

    2008-01-01

    Populations of the common killifish Fundulus heteroclitus are found along a latitudinal temperature gradient in habitats with high thermal variability. The objectives of this study were to assess the effects of temperature and population of origin on killifish swimming performance (assessed as critical swimming speed, U(crit)). Acclimated fish from northern and southern killifish populations demonstrated a wide zone (from 7 degrees to 33 degrees C) over which U(crit) showed little change with temperature, with performance declining significantly only at lower temperatures. Although we observed significant differences in swimming performance between a northern and a southern population of killifish in one experiment, with northern fish having an approximately 1.5-fold-greater U(crit) than southern fish across all acclimation temperatures, we were unable to replicate this finding in other populations or collection years, and performance was consistently high across all populations and at both low (7 degrees C) and high (23 degrees C) acclimation temperatures. The poor swimming performance of southern killifish from a single collection year was correlated with low muscle [glycogen] rather than with other indicators of fuel stores or body condition. Killifish acclimated to 18 degrees C and acutely challenged at temperatures of 5 degrees , 18 degrees , 25 degrees , or 34 degrees C showed modest thermal sensitivity of U(crit) between 18 degrees and 34 degrees C, with performance declining substantially at 5 degrees C. Thus, much of the zone of relative thermal insensitivity of swimming performance is intrinsic in this species rather than acquired as a result of acclimation. These data suggest that killifish are broadly tolerant of changing temperatures, whether acute or chronic, and demonstrate little evidence of local adaptation in endurance swimming performance in populations from different thermal habitats.

  4. Convergence in Underwater Swimming Between Nature and Engineering

    NASA Astrophysics Data System (ADS)

    Bandyopadhyay, Promode R.; Boller, Michael

    2004-11-01

    We are interested in comparing the hydrodynamic performance of underwater vehicles and swimming animals which are believed to have been optimized via evolution. Cruising and maneuvering are treated separately. Platforms like submarines are primarily cruising vehicles, while torpedoes are dexterous in both. In swimming animals, generally, red muscle is used for cruising while white muscle is used for maneuvering motions. Data from literature is examined comparing shaft/muscle power versus displacement. Experiments also have been carried out with captive mackerel and bluefish that are known to be open water fish and are proficient in both cruising and maneuvering. Their trajectories around obstacles have been recorded and analyzed. Similar figure of eight' maneuvering trajectory data of engineering underwater vehicles have also been analyzed. It is shown that there is convergence between nature and engineering in cruising that extend over eight decades of variation in power and displacement. However, swimming animals are still more proficient in maneuvering, although the gap has been closing of late.

  5. Imaging Techniques for Dense 3D reconstruction of Swimming Aquatic Life using Multi-view Stereo

    NASA Astrophysics Data System (ADS)

    Daily, David; Kiser, Jillian; McQueen, Sarah

    2016-11-01

    Understanding the movement characteristics of how various species of fish swim is an important step to uncovering how they propel themselves through the water. Previous methods have focused on profile capture methods or sparse 3D manual feature point tracking. This research uses an array of 30 cameras to automatically track hundreds of points on a fish as they swim in 3D using multi-view stereo. Blacktip sharks, sting rays, puffer fish, turtles and more were imaged in collaboration with the National Aquarium in Baltimore, Maryland using the multi-view stereo technique. The processes for data collection, camera synchronization, feature point extraction, 3D reconstruction, 3D alignment, biological considerations, and lessons learned will be presented. Preliminary results of the 3D reconstructions will be shown and future research into mathematically characterizing various bio-locomotive maneuvers will be discussed.

  6. Submerged swimming of the great cormorant Phalacrocorax carbo sinensis is a variant of the burst-and-glide gait.

    PubMed

    Ribak, Gal; Weihs, Daniel; Arad, Zeev

    2005-10-01

    Cormorants are water birds that forage by submerged swimming in search and pursuit of fish. Underwater they swim by paddling with both feet simultaneously in a gait that includes long glides between consecutive strokes. At shallow swimming depths the birds are highly buoyant as a consequence of their aerial lifestyle. To counter this buoyancy cormorants swim underwater with their body at an angle to the swimming direction. This mechanical solution for foraging at shallow depth is expected to increase the cost of swimming by increasing the drag of the birds. We used kinematic analysis of video sequences of cormorants swimming underwater at shallow depth in a controlled research setup to analyze the swimming gait and estimate the resultant drag of the birds during the entire paddling cycle. The gliding drag of the birds was estimated from swimming speed deceleration during the glide stage while the drag during active paddling was estimated using a mathematical ;burst-and-glide' model. The model was originally developed to estimate the energetic saving from combining glides with burst swimming and we used this fact to test whether the paddling gait of cormorants has similar advantages. We found that swimming speed was correlated with paddling frequency (r=0.56, P<0.001, N=95) where the increase in paddling frequency was achieved mainly by shortening the glide stage (r=-0.86, P<0.001, N=95). The drag coefficient of the birds during paddling was higher on average by two- to threefold than during gliding. However, the magnitude of the drag coefficient during the glide was positively correlated with the tilt of the body (r=0.5, P<0.003, N=35) and negatively correlated with swimming speed (r=-0.65, P<0.001, N=35), while the drag coefficient during the stroke was not correlated with tilt of the body (r=-0.11, P>0.5, N=35) and was positively correlated with swimming speed (r=0.41, P<0.015, N=35). Therefore, the difference between the drag coefficient during the glide and

  7. Behavior, metabolism and swimming physiology in juvenile Spinibarbus sinensis exposed to PFOS under different temperatures.

    PubMed

    Xia, Ji-Gang; Nie, Li-Juan; Mi, Xia-Mei; Wang, Wei-Zhen; Ma, Yi-Jie; Cao, Zhen-Dong; Fu, Shi-Jian

    2015-10-01

    The harmful effects of perfluorooctane sulfonate (PFOS) are of growing international concern. This paper aimed to gain an integrated understanding of fitness-related ecological end points, such as behavior, metabolism and swimming physiology, in juvenile Spinibarbus sinensis in response to PFOS toxicity at different temperatures. The fish were exposed to a range of PFOS concentrations (0, 0.32, 0.8, 2 and 5 mg/L) at different temperatures (18 and 28 °C) for 30 days. The effects on fish behavior, metabolic characteristics and aerobic swimming performance caused by PFOS at different temperatures were investigated. Our results showed that both PFOS and temperature had important influences on spontaneous swimming behavior, social interactions, routine metabolic rate (RMR), net energetic cost of transport (COTnet) and critical swimming speed (U crit) in fish. The lowest observed effect concentration for both U crit and RMR was 5 and 0.8 mg/L at 18 and 28 °C, respectively. We found that PFOS affected various behavioral and social end points and also appeared to affect metabolic rates and reduced U crit, likely as a result of increased COTnet, and that many of these effects also changed with respect to temperature. Our results further the understanding of the metabolic and behavioral toxicity of PFOS to aquatic organisms.

  8. Swim-training changes the spatio-temporal dynamics of skeletogenesis in zebrafish larvae (Danio rerio).

    PubMed

    Fiaz, Ansa W; Léon-Kloosterziel, Karen M; Gort, Gerrit; Schulte-Merker, Stefan; van Leeuwen, Johan L; Kranenbarg, Sander

    2012-01-01

    Fish larvae experience many environmental challenges during development such as variation in water velocity, food availability and predation. The rapid development of structures involved in feeding, respiration and swimming increases the chance of survival. It has been hypothesized that mechanical loading induced by muscle forces plays a role in prioritizing the development of these structures. Mechanical loading by muscle forces has been shown to affect larval and embryonic bone development in vertebrates, but these investigations were limited to the appendicular skeleton. To explore the role of mechanical load during chondrogenesis and osteogenesis of the cranial, axial and appendicular skeleton, we subjected zebrafish larvae to swim-training, which increases physical exercise levels and presumably also mechanical loads, from 5 until 14 days post fertilization. Here we show that an increased swimming activity accelerated growth, chondrogenesis and osteogenesis during larval development in zebrafish. Interestingly, swim-training accelerated both perichondral and intramembranous ossification. Furthermore, swim-training prioritized the formation of cartilage and bone structures in the head and tail region as well as the formation of elements in the anal and dorsal fins. This suggests that an increased swimming activity prioritized the development of structures which play an important role in swimming and thereby increasing the chance of survival in an environment where water velocity increases. Our study is the first to show that already during early zebrafish larval development, skeletal tissue in the cranial, axial and appendicular skeleton is competent to respond to swim-training due to increased water velocities. It demonstrates that changes in water flow conditions can result into significant spatio-temporal changes in skeletogenesis.

  9. Sensitization of the Tritonia escape swim.

    PubMed

    Frost, W N; Brandon, C L; Mongeluzi, D L

    1998-03-01

    When repeatedly elicited, the oscillatory escape swim of the marine mollusc Tritonia diomedea undergoes habituation of the number of cycles per swim. Previous work has shown that this habituation is accompanied by sensitization of another feature of the behavior: latency to swim onset. Here we focused on the behavioral features of sensitization itself. Test swims elicited 5 min after a strong sensitizing head stimulus differed in several ways from control swims: sensitized animals had shorter latencies for gill and rhinophore withdrawal, a shorter latency for swim onset, a lower threshold for swim initiation, and an increased number of cycles per swim. Sensitized animals did not, however, swim any faster (no change in cycle period). A separate experiment found that swim onset latency also sensitized when Tritonia came into contact with one of their natural predators, the seastar Pycnopodia helianthoides, demonstrating the ecological relevance of this form of nonassociative learning. These results define the set of behavioral changes to be explained by cellular studies of sensitization in Tritonia.

  10. On the efficient swimming of a ray-inspired underwater vehicle Part I: Experimental study on swimming optimization of control and fin structure

    NASA Astrophysics Data System (ADS)

    Zhu, Jianzhong; Lopez, Mervyn; Williams, Ventress; Aluko, Theophilus; Dong, Haibo; Bart-Smith, Hilary

    2014-11-01

    Batoid fish such as manta and cownose rays are among the most agile and energy efficient swimming creatures. These capabilities arise from flapping and bending their dorsally flattened pectoral fins. To assess this contribution, this study focuses on the study of a bio-inspired underwater vehicle--the MantaBot--where biological design criteria are applied. The MantaBot consists of two parts: a rigid body rendered from a CT scanning image of a cownose ray and two flexible fins driven by tensegrity actuators. The experiments were conducted in a water tank where the MantaBot was attached to a rail for rectilinear swimming. Three stereo-videos were taken and digitized to measure the 3D kinematics. Results showed that the fins conduct deformations in both spanwise and chordwise directions during steady swimming. Optimal operation conditions were determined for fastest swimming by surveying a wide range of parameters. Contributions of thrust generation and amplitude hindrance of various portions of the fin volume were examined. Additionally, fin tip structure, material and bending properties were studied for optimal swimming. This research was supported by the Office of Naval Research (ONR) under the Multidisciplinary University Research Initiative (MURI) Grant N00014-08-1-0642 and Grant N00014-14-1-0533.

  11. Swimming behaviour of the upside-down swimming catfish ( Synodontis nigriventris) at high-quality microgravity - A drop-tower experiment

    NASA Astrophysics Data System (ADS)

    Anken, R.; Hilbig, R.

    2009-07-01

    The catfish Synodontis nigriventris often shows a unique swimming behaviour in being oriented upside-down. When swimming near a (e.g., vertical) substrate, however, the animals orient themselves with their ventral side towards this substrate. This tendency is called ventral substrate response (VSR). The VSR does not only override the upside-down swimming behaviour but also the dorsal light response and the ventral light response. In the course of an earlier drop-tower experiment performed at ZARM (Bremen, Germany) using cichlid fish ( Oreochromis mossambicus), we had observed that about 90% of the animals revealed sensorimotor disorders (kinetotic swimming) due to the almost complete lack of gravity as a cue for orientation. In order to further assess the importance of the VSR for postural control in S. nigriventris when being located near a substrate, we subjected catfish in relatively small chambers to drop-tower flights. In contrast to our results regarding cichlid fish, S. nigriventris showed no kinetotic behaviour. This clearly suggests that the VSR overrides even vestibular input and possibly represents the most important single behavioural response in this species.

  12. Unsteady swimming of small organisms

    NASA Astrophysics Data System (ADS)

    Wang, Shiyan; Ardekani, Arezoo

    2012-11-01

    Small planktonic organisms ubiquitously display unsteady or impulsive motion to attack a prey or escape a predator in natural environments. Despite this, the role of unsteady hydrodynamic forces such as history and added mass forces on the low Reynolds number propulsion of small organisms is poorly understood. In this paper, we derive the fundamental equation of motion for an organism swimming by the means of surface distortion in a nonuniform flow at a low Reynolds number regime. We show that the history and added mass forces, that where traditionally neglected in the literature for small swimming organisms, cannot be neglected as the Stokes number increases above unity. For example, these unsteady inertial forces are of the same order as quasi-steady Stokes forces for Paramecium. Finally, we quantify the effects of convective inertial forces in the limit of small, but nonzero, Reynolds number regime. This work is supported by NSF grant CBET-1066545.

  13. Swimming near a deformable interface

    NASA Astrophysics Data System (ADS)

    Dias, Marcelo; Powers, Thomas

    2013-03-01

    It is a known fact that swimmers behave differently near deformable soft tissues than when near a rigid surface. Motivated by this class of problems, we investigate swimming microorganisms near flexible walls. We calculate the speed of a n infinitely long swimmer near an interface between two viscous fluids. Part of the calculation of the speed is the calculation of the shape of the free boundary. The swimming speed is controlled by the competition between surface and viscous effects, where two limits are observed. When the surface tension vanishes, we get Taylor's result for a swimmer with no walls. When the surface tension is infinite, the problem is like that of a swimmer near a rigid wall.

  14. Effects of chronic dietary selenomethionine exposure on repeat swimming performance, aerobic metabolism and methionine catabolism in adult zebrafish (Danio rerio).

    PubMed

    Thomas, Jith K; Wiseman, Steve; Giesy, John P; Janz, David M

    2013-04-15

    In a previous study we reported impaired swimming performance and greater stored energy in adult zebrafish (Danio rerio) after chronic dietary exposure to selenomethionine (SeMet). The goal of the present study was to further investigate effects of chronic exposure to dietary SeMet on repeat swimming performance, oxygen consumption (MO2), metabolic capacities (standard metabolic rate [SMR], active metabolic rate [AMR], factorial aerobic scope [F-AS] and cost of transport [COT]) and gene expression of energy metabolism and methionine catabolism enzymes in adult zebrafish. Fish were fed SeMet at measured concentrations of 1.3, 3.4, 9.8 or 27.5 μg Se/g dry mass (d.m.) for 90 d. At the end of the exposure period, fish from each treatment group were divided into three subgroups: (a) no swim, (b) swim, and (c) repeat swim. Fish from the no swim group were euthanized immediately at 90 d and whole body triglycerides, glycogen and lactate, and gene expression of energy metabolism and methionine catabolism enzymes were determined. Individual fish from the swim group were placed in a swim tunnel respirometer and swimming performance was assessed by determining the critical swimming speed (U(crit)). After both Ucrit and MO2 analyses, fish were euthanized and whole body energy stores and lactate were determined. Similarly, individual fish from the repeat swim group were subjected to two U(crit) tests (U(crit-1) and U(crit-2)) performed with a 60 min recovery period between tests, followed by determination of energy stores and lactate. Impaired swim performance was observed in fish fed SeMet at concentrations greater than 3 μg Se/g in the diet. However, within each dietary Se treatment group, no significant differences between single and repeat U(crits) were observed. Oxygen consumption, SMR and COT were significantly greater, and F-AS was significantly lesser, in fish fed SeMet. Whole body triglycerides were proportional to the concentration of SeMet in the diet. While

  15. Heart rate variability and swimming.

    PubMed

    Koenig, Julian; Jarczok, Marc N; Wasner, Mieke; Hillecke, Thomas K; Thayer, Julian F

    2014-10-01

    Professionals in the domain of swimming have a strong interest in implementing research methods in evaluating and improving training methods to maximize athletic performance and competitive outcome. Heart rate variability (HRV) has gained attention in research on sport and exercise to assess autonomic nervous system activity underlying physical activity and sports performance. Studies on swimming and HRV are rare. This review aims to summarize the current evidence on the application of HRV in swimming research and draws implications for future research. A systematic search of databases (PubMed via MEDLINE, PSYNDEX and Embase) according to the PRISMA statement was employed. Studies were screened for eligibility on inclusion criteria: (a) empirical investigation (HRV) in humans (non-clinical); (b) related to swimming; (c) peer-reviewed journal; and (d) English language. The search revealed 194 studies (duplicates removed), of which the abstract was screened for eligibility. Fourteen studies meeting the inclusion criteria were included in the review. Included studies broadly fell into three classes: (1) control group designs to investigate between-subject differences (i.e. swimmers vs. non-swimmers, swimmers vs. other athletes); (2) repeated measures designs on within-subject differences of interventional studies measuring HRV to address different modalities of training or recovery; and (3) other studies, on the agreement of HRV with other measures. The feasibility and possibilities of HRV within this particular field of application are well documented within the existing literature. Future studies, focusing on translational approaches that transfer current evidence in general practice (i.e. training of athletes) are needed.

  16. Traits of acoustic signalization and generation of sounds by some schooling physostomous fish

    NASA Astrophysics Data System (ADS)

    Kuznetsov, M. Yu.

    2009-11-01

    The results of experimental investigations of acoustic activity of schooling physostomous fish are discussed, made with reference to chum salmon, pink salmon, Pacific herring, and sardine. Dynamic spectra of most investigated fish are concentrated within two subranges of frequency, according to each investigated fish species. Direct participation of the swimming bladder in sound formation in the investigated fish is shown. Morphological traits of sound-producing organs of salmons and herrings are considered. Mechanisms of generation of signals in physotmous fish involving the muscular sphincter and swimming bladder are analyzed.

  17. Planktivorous Fish Recognize Temporal Motion Patterns of Suspended Particles

    NASA Astrophysics Data System (ADS)

    Strickler, J. R.; Tsonis, A.

    2004-12-01

    Small planktivorous fish feed by selective captures of individual zooplankters. We realize that: 1) the predator, as well as the prey is suspended in the water column, which does not provide either with stable reference points; 2) the ambient flow field acts differently on the larger predators than on the much smaller prey; and 3) within the water column there are many suspended particles of lower nutritional value than the zooplankters represent. We investigated in the laboratory whether or not fish can distinguish between small targets moving with different swimming patterns, e.g. particles entrained passively in the ambient water flow versus entrained but actively swimming particles. We created in an aquarium computer-animated stimuli with motion patterns ranging from random to actual swimming motions of live animals. The results show that planktivorous fish can recognize temporal patterns in a visually homogeneous environment. Therefore, blue-water fish must process visual information similar to terrestrial animals processing auditory information.

  18. How many fish in a tank? Constructing an automated fish counting system by using PTV analysis

    NASA Astrophysics Data System (ADS)

    Abe, S.; Takagi, T.; Takehara, K.; Kimura, N.; Hiraishi, T.; Komeyama, K.; Torisawa, S.; Asaumi, S.

    2017-02-01

    Because escape from a net cage and mortality are constant problems in fish farming, health control and management of facilities are important in aquaculture. In particular, the development of an accurate fish counting system has been strongly desired for the Pacific Bluefin tuna farming industry owing to the high market value of these fish. The current fish counting method, which involves human counting, results in poor accuracy; moreover, the method is cumbersome because the aquaculture net cage is so large that fish can only be counted when they move to another net cage. Therefore, we have developed an automated fish counting system by applying particle tracking velocimetry (PTV) analysis to a shoal of swimming fish inside a net cage. In essence, we treated the swimming fish as tracer particles and estimated the number of fish by analyzing the corresponding motion vectors. The proposed fish counting system comprises two main components: image processing and motion analysis, where the image-processing component abstracts the foreground and the motion analysis component traces the individual's motion. In this study, we developed a Region Extraction and Centroid Computation (RECC) method and a Kalman filter and Chi-square (KC) test for the two main components. To evaluate the efficiency of our method, we constructed a closed system, placed an underwater video camera with a spherical curved lens at the bottom of the tank, and recorded a 360° view of a swimming school of Japanese rice fish (Oryzias latipes). Our study showed that almost all fish could be abstracted by the RECC method and the motion vectors could be calculated by the KC test. The recognition rate was approximately 90% when more than 180 individuals were observed within the frame of the video camera. These results suggest that the presented method has potential application as a fish counting system for industrial aquaculture.

  19. Divers swimming efficiency as a function of buoyancy, swimming attitude, protective garments, breathing apparatus, swimming technique and fin type’.

    DTIC Science & Technology

    1993-12-15

    38 mlo2/kg/mile), the energy cost of underwater swimming varies greatly between swimmers and is dependent upon their technique. There is no way for...clad swimmers swimming at a moderate speed. MEASUREMENT OF OXYGEN CONSUMPTION Previous studies have used the drop in tank pressure to determine the...laboratory, we developed a method of determining the body drag and efficiency of swimmers while they were actually swimming. This technique is based on

  20. Nutritional recommendations for synchronized swimming.

    PubMed

    Robertson, Sherry; Benardot, Dan; Mountjoy, Margo

    2014-08-01

    The sport of synchronized swimming is unique, because it combines speed, power, and endurance with precise synchronized movements and high-risk acrobatic maneuvers. Athletes must train and compete while spending a great amount of time underwater, upside down, and without the luxury of easily available oxygen. This review assesses the scientific evidence with respect to the physiological demands, energy expenditure, and body composition in these athletes. The role of appropriate energy requirements and guidelines for carbohydrate, protein, fat, and micronutrients for elite synchronized swimmers are reviewed. Because of the aesthetic nature of the sport, which prioritizes leanness, the risks of energy and macronutrient deficiencies are of significant concern. Relative Energy Deficiency in Sport and disordered eating/eating disorders are also of concern for these female athletes. An approach to the healthy management of body composition in synchronized swimming is outlined. Synchronized swimmers should be encouraged to consume a well-balanced diet with sufficient energy to meet demands and to time the intake of carbohydrate, protein, and fat to optimize performance and body composition. Micronutrients of concern for this female athlete population include iron, calcium, and vitamin D. This article reviews the physiological demands of synchronized swimming and makes nutritional recommendations for recovery, training, and competition to help optimize athletic performance and to reduce risks for weight-related medical issues that are of particular concern for elite synchronized swimmers.

  1. Exposure to sublethal levels of PCB-126 impacts fuel metabolism and swimming performance in rainbow trout.

    PubMed

    Bellehumeur, Karyne; Lapointe, Dominique; Cooke, Steven J; Moon, Thomas W

    2016-09-01

    Polychlorinated biphenyls (PCBs) are recognized physiological stressors to fish which over time may impair individual performance and perhaps fitness by inducing changes that could have population-level consequences. PCB-126 (3,3',4,4',5-pentachlorobiphenyl) accumulates in lipids and can subsequently be released into the bloodstream during periods of high activity that involve the mobilization of stored fuels to meet with increasing energy demands. The goal of this study was to determine if a sublethal exposure to PCB-126 altered the content of tissue energy supplies (carbohydrates, proteins, amino acids, triglycerides) and impaired swimming performance as well as oxygen consumption in rainbow trout (Oncorhynchus mykiss). Trout were injected intraperitoneally with a single Low (100μgkg(-1)) or High (400μgkg(-1)) dose of PCB-126 then swimming performance and metabolic rates from 1 to 9days post-injection were compared to Control (non-dosed) fish. Liver ethoxyresorufin-O-deethylase (EROD) activity was assessed as an indication of PCB-126 intoxication while plasma and white muscle tissue metabolites were analyzed as an index of physiological disturbance. Swimming performance, assessed using two successive modified critical swimming speed (Ucrit) tests, was highest for fish in the High PCB-126 treatment; however, their initial condition factor (K) was also higher, largely due to their greater body mass. Trout in the High and Low PCB-126 treatments exhibited impaired recovery following intense exercise as they swam comparatively poorly when provided a second challenge. PCB-exposed fish exhibited reduced spleen somatic indices as well as muscle glucose and glycogen contents; whereas plasma cortisol and glucose levels were elevated, indicating higher metabolic costs during recovery and muscle restoration. Overall, this research provides insights into the sublethal effects of a toxic organic compound on swimming performance in trout. Copyright © 2016 Elsevier Inc. All

  2. Kinematics of swimming garter snakes (Thamnophis sirtalis).

    PubMed

    Munk, Yonatan

    2008-06-01

    We investigate the kinematics of swimming garter snakes (Thamnophis sirtalis) using a novel nonlinear regression-based digitization method to establish quantitative statistical support for non-constant wavelengths in the undulatory pattern exhibited by swimming snakes. We find that in swimming snakes, the growth of the amplitude of the propulsive wave head-to-tail is strongly correlated (p < 0.005) with the head-to-tail growth in the wavelength. We investigate correlations between kinematic parameters and steady swimming speed, and find a very strong positive correlation between swimming speed and undulation frequency. We furthermore find a statistically well-supported positive correlation between swimming speed and both the initial amplitude of the propulsive wave at the head and the degree of amplitude growth from head to tail.

  3. Evolution of intrinsic growth and energy acquisition rates. I. Trade-offs with swimming performance in Menidia menidia.

    PubMed

    Billerbeck, J M; Lankford, T E; Conover, D O

    2001-09-01

    Latitudinal populations of the Atlantic silverside, Menidia menidia, show substantial genetic variation in rates of energy acquistion and allocation. Reared in common environments, silversides from northern latitudes consume more food, grow faster and more efficiently, store more energy, and produce greater quantities of eggs than their southern conspecifics. The persistence of seemingly inferior southern genotypes in the face of ostensibly superior northern genotypes suggest that there are hidden evolutionary trade-offs associated with these elevated acquisition and allocation rates. We tested the hypothesis that rapid growth and high levels of food consumption trade-off against locomotory performance in M. menidia. We compared both aerobic (prolonged and endurance) and anaerobic (burst) swimming capacities between intrinsically fast-growing fish from the north (Nova Scotia, NS) and intrinsically slow-growing fish from the south (South Carolina, SC) and between growth-manipulated phenotypes within each population. We also compared swimming speeds and endurance between fasted and recently fed fish within populations. Maximum prolonged and burst swimming speeds of NS fish were significantly lower than those of SC fish, and swimming speeds of fast-growing phenotypes were lower than those of slow-growing phenotypes within populations. Fed fish had lower burst speeds and less endurance than fasted fish from the same population. Thus, high rates of growth and the consumption of large meals clearly diminish swimming performance, which likely increases vulnerability to predation and decreases survival and relative fitness. The submaximal growth rate of southern M. menidia appears to be adaptive, resulting from balancing selection on rates of somatic growth.

  4. Physiological responses of juvenile rainbow trout to fasting and swimming activity: Effects on body composition and condition indices

    USGS Publications Warehouse

    Simpkins, D.G.; Hubert, W.A.; Del Rio, C.M.; Rule, D.C.

    2003-01-01

    The physiological traits that allow fish to survive periods of limited food resources are poorly understood. We assessed changes in proximate body composition, relative organ mass, blood metabolites, and relative weight (Wr) of sedentary and actively swimming (15 cm/s) juvenile rainbow trout (154-182 mm total length) over 147 d of fasting. Fasting caused measurable responses that were augmented when fish were swimming. Lipids and plasma triacylglycerides declined over time. Proteins were catabolized simultaneously with lipid reserves, but ammonia concentrations in plasma did not increase. The liver somatic index (LSI) did not change substantially over 105 d, suggesting that gluconeogenesis maintained blood glucose concentrations and hepatic glycogen reserves for a substantial period of fasting. The gut somatic index (GSI) and Wr declined linearly during fasting, but the LSI did not decline until after 105 d of fasting. Consequently, the use of different body condition indices could lead to different conclusions about the condition of juvenile rainbow trout. Swimming activity caused fish to have lower lipid and protein reserves than those of sedentary fish. No mortalities were observed among sedentary fish, but mortalities occurred among actively swimming fish after 97 d of fasting when 3.2% or less lipid remained in their bodies. Body condition indices did not account for differences in proximate body composition between sedentary and actively swimming fish and were relatively poor predictors of lipid content and risk of mortality. The probability of mortality was most accurately predicted by percent lipid content. Therefore, we suggest that fisheries scientists consider using percent lipid content when evaluating the physiological status and risk of mortality due to starvation among juvenile rainbow trout.

  5. Unilateral ablation of trunk superficial neuromasts increases directional instability during steady swimming in the yellowtail kingfish Seriola lalandi.

    PubMed

    Yanase, K; Herbert, N A; Montgomery, J C

    2014-09-01

    Detailed swimming kinematics of the yellowtail kingfish Seriola lalandi were investigated after unilateral ablation of superficial neuromasts (SNs). Most kinematic variables, such as tail-beat frequency, stride length, caudal fin-beat amplitude and propulsive wavelength, were unaffected but lateral amplitude at the tip of the snout (A0 ) was significantly increased in SN-disrupted fish compared with sham-operated controls. In addition, the orientation of caudal fin-tip relative to the overall swimming direction of SN-disrupted fish was significantly deflected (two-fold) in comparison with sham-operated control fish. In some fish, SN disruption also led to a phase distortion of the propulsive body-wave. These changes would be expected to increase both hydrodynamic drag and thrust production which is consistent with the finding that SN-disrupted fish had to generate significantly greater thrust power when swimming at ≥1·3 fork lengths (LF ) s(-1) . In particular, hydrodynamic drag would increase as a result of any increase in rotational (yaw) perturbation and sideways slip resulting from the sensory disturbance. In conclusion, unilateral SN ablation produced directional instability of steady swimming and altered propulsive movements, suggesting a role for sensory feedback in correcting yaw and slip disturbances to maintain efficient locomotion.

  6. A Minimalistic Approach to Swimming Through Sand

    NASA Astrophysics Data System (ADS)

    Bzdega, Matt; Koehler, Stephan

    2005-11-01

    Inspired by microorganisms swimming at low Reynolds, we are interested in understanding how self-propelled robots can swim through sand. We find that a two-hinged swimmer can propel itself forwards and backwards through a simple sequence of cyclically repeated stroking motions. A range of parameters including paddle size, shape, and stroking angles, along with variations of the swimming strategies were investigated and the results show similarities to Purcell's two-hinged swimmer.

  7. Swimming Pool Survey, Offutt AFB, Nebraska.

    DTIC Science & Technology

    1987-12-01

    70-RIl9 236 SWIMMING POOL SIEVEY OFFUTT NWD NEURASIR(U) AIR FORCE 1/1 OCCUIPATIONAL AND EIWIRONHENTAL HEALTH LAIDBOOKS NFl TX ft 0 INGY! DEC 87... test in swimming pool evaluations to determine the severity of’ future contamination problems. C. In order to maintain pool water stability...154EQ0146MSB I4 Swimming Pool Survey, Offutt AFB NE ROBERT D. BINOVI, Lt Col, USAF, BSC vTO ELECTEOEC 3 1197 ,: i December 1987 Final Report Distribution

  8. Examining dolphin hydrodynamics provides clues to calf-loss during tuna fishing

    PubMed Central

    Moore, Pete

    2004-01-01

    A combination of mathematical modeling and direct observation of the swimming behavior of dolphin mother-calf pairs has shown how the calf can gain much of the energy required for swimming if it is positioned correctly relative to the mother, a situation that may be disrupted during the chases that result from tuna-fishing practices. PMID:15132739

  9. Floppy swimming: viscous locomotion of actuated elastica.

    PubMed

    Lauga, Eric

    2007-04-01

    Actuating periodically an elastic filament in a viscous liquid generally breaks the constraints of Purcell's scallop theorem, resulting in the generation of a net propulsive force. This observation suggests a method to design simple swimming devices-which we call "elastic swimmers"-where the actuation mechanism is embedded in a solid body and the resulting swimmer is free to move. In this paper, we study theoretically the kinematics of elastic swimming. After discussing the basic physical picture of the phenomenon and the expected scaling relationships, we derive analytically the elastic swimming velocities in the limit of small actuation amplitude. The emphasis is on the coupling between the two unknowns of the problems-namely the shape of the elastic filament and the swimming kinematics-which have to be solved simultaneously. We then compute the performance of the resulting swimming device and its dependence on geometry. The optimal actuation frequency and body shapes are derived and a discussion of filament shapes and internal torques is presented. Swimming using multiple elastic filaments is discussed, and simple strategies are presented which result in straight swimming trajectories. Finally, we compare the performance of elastic swimming with that of swimming micro-organisms.

  10. One Fish Two Fish.

    ERIC Educational Resources Information Center

    Hoffman, Michele

    1998-01-01

    This activity explains fisheries resource management to seven-year olds. First-grade students learn concepts such as offspring viability, life expectancy, and distribution of species, which help to determine when, where, and how people fish and the importance of fishing responsibly. Lists materials, procedures, and extensions. (SJR)

  11. One Fish Two Fish.

    ERIC Educational Resources Information Center

    Hoffman, Michele

    1998-01-01

    This activity explains fisheries resource management to seven-year olds. First-grade students learn concepts such as offspring viability, life expectancy, and distribution of species, which help to determine when, where, and how people fish and the importance of fishing responsibly. Lists materials, procedures, and extensions. (SJR)

  12. Swimming-Induced Taste Aversion and Its Prevention by a Prior History of Swimming

    ERIC Educational Resources Information Center

    Masaki, Takahisa; Nakajima, Sadahiko

    2004-01-01

    In two experiments, the evidence showed that 20 min of forced swimming by rats caused aversion to a taste solution consumed before swimming. When one of two taste solutions (sodium saccharin or sodium chloride, counterbalanced across rats) was paired with swimming and the other was not, the rats' intakes of these two solutions showed less…

  13. Swimming-Induced Taste Aversion and Its Prevention by a Prior History of Swimming

    ERIC Educational Resources Information Center

    Masaki, Takahisa; Nakajima, Sadahiko

    2004-01-01

    In two experiments, the evidence showed that 20 min of forced swimming by rats caused aversion to a taste solution consumed before swimming. When one of two taste solutions (sodium saccharin or sodium chloride, counterbalanced across rats) was paired with swimming and the other was not, the rats' intakes of these two solutions showed less…

  14. The Fish may be Used in the Space System

    NASA Astrophysics Data System (ADS)

    Liu, Chungchu; Liu, Xiaofeng; Lin, Zhongning

    Scientists in Space area like to grow fish in the biosphere, but they worry about that fish will contest oxygen with humans. Therefore growing low-oxygen-needing fish is very important. After research, we found a fish which may be a promising fish used in space system. This fish can grow normally under 1mg O2/1000 mg water oxygen condition while other species of fish die away. How to keep astronauts healthy and having delicious food are problem to raise life qualities of astronauts in space. Our pharmacological test shows that this chosen fish, with high DHA and EPA, in general, other fresh-water fish has low DHA and EPA. It has functions of anti-radiation and anti-tumor. It can also prolong cruor time, anoxia-tolerating, and swimming time after the mice feeding with the fish's meat.

  15. Forced sustained swimming exercise at optimal speed enhances growth of juvenile yellowtail kingfish (Seriola lalandi)

    PubMed Central

    Palstra, Arjan P.; Mes, Daan; Kusters, Kasper; Roques, Jonathan A. C.; Flik, Gert; Kloet, Kees; Blonk, Robbert J. W.

    2015-01-01

    Swimming exercise at optimal speed may optimize growth performance of yellowtail kingfish in a recirculating aquaculture system. Therefore, optimal swimming speeds (Uopt in m s−1 or body lengths s−1, BL s−1) were assessed and then applied to determine the effects of long-term forced and sustained swimming at Uopt on growth performance of juvenile yellowtail kingfish. Uopt was quantified in Blazka-type swim-tunnels for 145, 206, and 311 mm juveniles resulting in values of: (1) 0.70 m s−1 or 4.83 BL s−1, (2) 0.82 m s−1 or 3.25 BL s−1, and (3) 0.85 m s−1 or 2.73 BL s−1. Combined with literature data from larger fish, a relation of Uopt (BL s−1) = 234.07(BL)−0.779 (R2 = 0.9909) was established for this species. Yellowtail kingfish, either forced to perform sustained swimming exercise at an optimal speed of 2.46 BL s−1 (“swimmers”) or allowed to perform spontaneous activity at low water flow (“resters”) in a newly designed 3600 L oval flume (with flow created by an impeller driven by an electric motor), were then compared. At the start of the experiment, ten fish were sampled representing the initial condition. After 18 days, swimmers (n = 23) showed a 92% greater increase in BL and 46% greater increase in BW as compared to resters (n = 23). As both groups were fed equal rations, feed conversion ratio (FCR) for swimmers was 1.21 vs. 1.74 for resters. Doppler ultrasound imaging showed a statistically significant higher blood flow (31%) in the ventral aorta of swimmers vs. resters (44 ± 3 vs. 34 ± 3 mL min−1, respectively, under anesthesia). Thus, growth performance can be rapidly improved by optimal swimming, without larger feed investments. PMID:25620933

  16. Forced sustained swimming exercise at optimal speed enhances growth of juvenile yellowtail kingfish (Seriola lalandi).

    PubMed

    Palstra, Arjan P; Mes, Daan; Kusters, Kasper; Roques, Jonathan A C; Flik, Gert; Kloet, Kees; Blonk, Robbert J W

    2014-01-01

    Swimming exercise at optimal speed may optimize growth performance of yellowtail kingfish in a recirculating aquaculture system. Therefore, optimal swimming speeds (U opt in m s(-1) or body lengths s(-1), BL s(-1)) were assessed and then applied to determine the effects of long-term forced and sustained swimming at U opt on growth performance of juvenile yellowtail kingfish. U opt was quantified in Blazka-type swim-tunnels for 145, 206, and 311 mm juveniles resulting in values of: (1) 0.70 m s(-1) or 4.83 BL s(-1), (2) 0.82 m s(-1) or 3.25 BL s(-1), and (3) 0.85 m s(-1) or 2.73 BL s(-1). Combined with literature data from larger fish, a relation of U opt (BL s(-1)) = 234.07(BL)(-0.779) (R (2) = 0.9909) was established for this species. Yellowtail kingfish, either forced to perform sustained swimming exercise at an optimal speed of 2.46 BL s(-1) ("swimmers") or allowed to perform spontaneous activity at low water flow ("resters") in a newly designed 3600 L oval flume (with flow created by an impeller driven by an electric motor), were then compared. At the start of the experiment, ten fish were sampled representing the initial condition. After 18 days, swimmers (n = 23) showed a 92% greater increase in BL and 46% greater increase in BW as compared to resters (n = 23). As both groups were fed equal rations, feed conversion ratio (FCR) for swimmers was 1.21 vs. 1.74 for resters. Doppler ultrasound imaging showed a statistically significant higher blood flow (31%) in the ventral aorta of swimmers vs. resters (44 ± 3 vs. 34 ± 3 mL min(-1), respectively, under anesthesia). Thus, growth performance can be rapidly improved by optimal swimming, without larger feed investments.

  17. Arm insulation and swimming in cold water.

    PubMed

    Lounsbury, David S; Ducharme, Michel B

    2008-09-01

    To test whether adding insulation to the arms would improve cold water swimming performance by delaying swimming failure (SF). Novice (n = 7) and expert (n = 8) swimmers, clothed and equipped with a personal flotation device, each performed two trials in a swimming flume filled with 10 degrees C water. During free swimming (FS), subjects performed swimming until failure, followed by the Heat Escape Lessening Posture. In free swimming with additional insulation (FSA), subjects wore custom-fitted armbands. Trials ended when rectal temperature decreased to 34 degrees C or after 2 h of immersion. Measurements included: rectal and skin temperatures, heat flow, and various appraisals of swimming performance. FSA was thermally advantageous versus FS. Rectal temperature cooling rates during swimming (dT/dt Swim) were faster for FS compared to FSA (0.050 +/- 0.007 degrees C min(-1) vs. 0.042 +/- 0.006 degrees C min(-1), P < 0.01). Armbands maintained arm skin temperature about 10 degrees C warmer, for approximately 70 min (P < 0.001). Although additional insulation did not greatly improve physical performances, video analysis showed that swimming technique in FSA was maintained 10-15% better than in FS between minutes 30 and 50 (P < 0.001). SF was achieved in 5/30 trials, with increases in stroke rate (6.6 str min(-1)) and decreases in stroke length (0.24 m str(-1)) observed. In this simulation of cold water swimming survival, equipping subjects with neoprene armbands appears to have partially preserved muscle function, but with unimpressive effects on overall performance. SF is a complex entity, but is evidently related to both triceps skinfold and arm girth.

  18. Lumbar pain and fin swimming.

    PubMed

    Verni, E; Prosperi, L; Lucaccini, C; Fedele, L; Beluzzi, R; Lubich, T

    1999-03-01

    It was hypothesised that fin swimming have unique physiopathologic features in particular concerning low back involvement. Retrospective study. elite competitive fin swimmers. 17 males and 14 females aged from 16 to 23 years. piroxicam, sport interruption for a week, proper warming-up and wearing suggestions during out-of-water exercises in the symptomatic group. Absence of intervention in the asymptomatic one. anthropometric measures (weight, height, legs length discrepancy), isokinetic measures (trunk flexor/extensor ratio) and conventional radiological investigation were taken for all subjects. Low back pain was present in 14 subjects during off season but only 7 referred discomfort in competitive season. 78.5% of symptomatic subjects showed radiological abnormalities while imaging changes were present in 52.9% of the asymptomatic group. Flexor/extensor ratio isokinetically evaluated was less than one in 6 athletes complaining back discomfort. Non steroid medication, physiotherapy, training and wearing cares was suggested. Authors report a pain free return to competition in 57% and a partial resolution in 28% of those symptomatic cases who were not used to training cares (in particular proper "out-of-water" warming up) and wearing precautions (complete wiping and suitable thermic clothing after swimming). In fin swimming low back pain can be related to the existence of environmental and intrinsic factors. In our series no significant difference in imaging changes was pointed out among asymptomatic or painful athletes. Therefore a cyclic load on the column, in absence of training precautions can make spine abnormalities (in particular schisis, facet derangement and pars lesion) symptomatic.

  19. A Comparative Analysis of Swimming Styles in Competitive Swimming

    NASA Astrophysics Data System (ADS)

    von Loebbecke, Alfred; Mittal, Rajat; Gupta, Varun; Mark, Russell

    2007-11-01

    High-fidelity numerical simulations are being used to conduct a critical evaluation of swimming strokes in competitive swimming. We combine computational fluid dynamics (CFD), laser body scans, animation software, and video footage to develop accurate models of Olympic level swimmers and use these to examine contrasting styles of the dolphin kick as well as the arm strokes in back and front crawl stroke. In the dolphin kick, the focus is on examining the effects of Strouhal number, kick amplitude, frequency, and technique on thrust production. In the back stroke, we examine the performance of the so called ``flat stroke'' versus the ``deep catch,'' The most important aspect that separates the two major types of back stroke is the alignment or angle of attack of the palm during the stroke. In one style of front crawl arm stroke, there is greater elbow joint flexion, shoulder abduction and sculling whereas the other style consists of a straight arm pull dominated by simple shoulder flexion. Underlying the use of these two styles is the larger and more fundamental issue of the role of lift versus drag in thrust production and we use the current simulations to examine this issue in detail.

  20. Cruise and turning performance of an improved fish robot actuated by piezoceramic actuators

    NASA Astrophysics Data System (ADS)

    Nguyen, Quang Sang; Heo, Seok; Park, Hoon Cheol; Goo, Nam Seo; Byun, Doyoung

    2009-03-01

    The purpose of this study is improvement of a fish robot actuated by four light-weight piezocomposite actuators (LIPCAs). In the fish robot, we developed a new actuation mechanism working without any gear and thus the actuation mechanism was simple in fabrication. By using the new actuation mechanism, cross section of the fish robot became 30% smaller than that of the previous model. Performance tests of the fish robot in water were carried out to measure tail-beat angle, thrust force, swimming speed and turning radius for tail-beat frequencies from 1Hz to 5Hz. The maximum swimming speed of the fish robot was 7.7 cm/s at 3.9Hz tail-beat frequency. Turning experiment showed that swimming direction of the fish robot could be controlled with 0.41 m turning radius by controlling tail-beat angle.

  1. Performance evaluation of an improved fish robot actuated by piezoceramic actuators

    NASA Astrophysics Data System (ADS)

    Nguyen, Q. S.; Heo, S.; Park, H. C.; Byun, D.

    2010-03-01

    This paper presents an improved fish robot actuated by four lightweight piezocomposite actuators. Our newly developed actuation mechanism is simple to fabricate because it works without gears. With the new actuation mechanism, the fish robot has a 30% smaller cross section than our previous model. Performance tests of the fish robot in water were carried out to measure the tail-beat angle, the thrust force, the swimming speed for various tail-beat frequencies from 1 to 5 Hz and the turning radius at the optimal frequency. The maximum swimming speed of the fish robot is 7.7 cm s - 1 at a tail-beat frequency of 3.9 Hz. A turning experiment shows that the swimming direction of the fish robot can be controlled by changing the duty ratio of the driving voltage; the fish robot has a turning radius of 0.41 m for a left turn and 0.68 m for a right turn.

  2. Neuromuscular Control of Rapid Linear Accelerations in Fish

    DTIC Science & Technology

    2016-06-22

    gathered a large amount of data during the nine months of this project: steady swimming and acceleration behaviors from five fishes with high speed video...IMUs, and electromyography electrodes, and the behaviors from three fish with high speed video, IMUs, and particle image velocimetry. Data analysis is...moderate accelerations, at three or four positions along both sides of the body (6 or 8 electrodes total). Fish were filmed at high speed from below

  3. The archaellum: how Archaea swim.

    PubMed

    Albers, Sonja-Verena; Jarrell, Ken F

    2015-01-01

    Recent studies on archaeal motility have shown that the archaeal motility structure is unique in several aspects. Although it fulfills the same swimming function as the bacterial flagellum, it is evolutionarily and structurally related to the type IV pilus. This was the basis for the recent proposal to term the archaeal motility structure the "archaellum." This review illustrates the key findings that led to the realization that the archaellum was a novel motility structure and presents the current knowledge about the structural composition, mechanism of assembly and regulation, and the posttranslational modifications of archaella.

  4. Upstream Swimming in Microbiological Flows.

    PubMed

    Mathijssen, Arnold J T M; Shendruk, Tyler N; Yeomans, Julia M; Doostmohammadi, Amin

    2016-01-15

    Interactions between microorganisms and their complex flowing environments are essential in many biological systems. We develop a model for microswimmer dynamics in non-Newtonian Poiseuille flows. We predict that swimmers in shear-thickening (-thinning) fluids migrate upstream more (less) quickly than in Newtonian fluids and demonstrate that viscoelastic normal stress differences reorient swimmers causing them to migrate upstream at the centerline, in contrast to well-known boundary accumulation in quiescent Newtonian fluids. Based on these observations, we suggest a sorting mechanism to select microbes by swimming speed.

  5. Upstream Swimming in Microbiological Flows

    NASA Astrophysics Data System (ADS)

    Mathijssen, Arnold J. T. M.; Shendruk, Tyler N.; Yeomans, Julia M.; Doostmohammadi, Amin

    2016-01-01

    Interactions between microorganisms and their complex flowing environments are essential in many biological systems. We develop a model for microswimmer dynamics in non-Newtonian Poiseuille flows. We predict that swimmers in shear-thickening (-thinning) fluids migrate upstream more (less) quickly than in Newtonian fluids and demonstrate that viscoelastic normal stress differences reorient swimmers causing them to migrate upstream at the centerline, in contrast to well-known boundary accumulation in quiescent Newtonian fluids. Based on these observations, we suggest a sorting mechanism to select microbes by swimming speed.

  6. The archaellum: how Archaea swim

    PubMed Central

    Albers, Sonja-Verena; Jarrell, Ken F.

    2015-01-01

    Recent studies on archaeal motility have shown that the archaeal motility structure is unique in several aspects. Although it fulfills the same swimming function as the bacterial flagellum, it is evolutionarily and structurally related to the type IV pilus. This was the basis for the recent proposal to term the archaeal motility structure the “archaellum.” This review illustrates the key findings that led to the realization that the archaellum was a novel motility structure and presents the current knowledge about the structural composition, mechanism of assembly and regulation, and the posttranslational modifications of archaella. PMID:25699024

  7. Undulatory swimming in viscoelastic fluids.

    PubMed

    Shen, X N; Arratia, P E

    2011-05-20

    The effects of fluid elasticity on the swimming behavior of the nematode Caenorhabditis elegans are experimentally investigated by tracking the nematode's motion and measuring the corresponding velocity fields. We find that fluid elasticity hinders self-propulsion. Compared to Newtonian solutions, fluid elasticity leads to up to 35% slower propulsion. Furthermore, self-propulsion decreases as elastic stresses grow in magnitude in the fluid. This decrease in self-propulsion in viscoelastic fluids is related to the stretching of flexible molecules near hyperbolic points in the flow.

  8. Anguilliform fish propulsion of highest hydrodynamic efficiency

    NASA Astrophysics Data System (ADS)

    Vorus, William S.; Taravella, Brandon M.

    2011-06-01

    It is hypothesized that steady anguilliform swimming motion of aquatic animals is purely reactive such that no net vortex wake is left downstream. This is versus carangiform and tunniform swimming of fish, where vortex streams are shed from tail, fins, and body. But there the animal movements are such to produce partial vortex cancellation downstream in maximizing propulsive efficiency. In anguilliform swimming characteristic of the eel family, it is argued that the swimming motions are configured by the animal such that vortex shedding does not occur at all. However, the propulsive thrust in this case is higher order in the motion amplitude, so that relatively large coils are needed to produce relatively small thrust; the speeds of anguilliform swimmers are less than the carangiform and tunniform, which develop first order thrusts via lifting processes. Results of experimentation on live lamprey are compared to theoretical prediction which assumes the no-wake hypothesis. Two-dimensional analysis is first performed to set the concept. This is followed by three-dimensional analysis using slender-body theory. Slender-body theory has been applied by others in studying anguilliform swimming, as it is ideally suited to the geometry of the lamprey and other eel-like animals. The agreement between this new approach based on the hypothesis of wakeless swimming and the experiments is remarkably good in spite of the physical complexities.

  9. Comparing effects of transmitters within and among populations: application to swimming performance of juvenile Chinook salmon

    USGS Publications Warehouse

    Perry, Russell W.; Plumb, John M.; Fielding, Scott D.; Adams, Noah S.; Rondorf, Dennis W.

    2013-01-01

    The sensitivity of fish to a transmitter depends on factors such as environmental conditions, fish morphology, life stage, rearing history, and tag design. However, synthesizing general trends across studies is difficult because each study focuses on a particular performance measure, species, life stage, and transmitter model. These differences motivated us to develop simple metrics that allow effects of transmitters to be compared among different species, populations, or studies. First, we describe how multiple regression analysis can be used to quantify the effect of tag burden (transmitter mass relative to fish mass) on measures of physiological performance. Next, we illustrate how the slope and intercept parameters can be used to calculate two summary statistics: θ, which estimates the tag burden threshold above which the performance of tagged fish begins to decline relative to untagged fish; and k, which measures the percentage change in performance per percentage point increase in tag burden. When θ = 0, k provides a single measure of the tag's effect that can be compared among species, populations, or studies. We apply this analysis to two different experiments that measure the critical swimming speed (U crit) of tagged juvenile Chinook Salmon Oncorhynchus tshawytscha. In both experiments, U crit declined as tag burden increased, but we found no significant threshold in swimming performance. Estimates of θ ranged from −0.6% to 2.1% among six unique treatment groups, indicating that swimming performance began to decline at a relatively low tag burden. Estimates of k revealed that U crit of tagged fish declined by −2.68% to −4.86% for each 1% increase in tag burden. Both θ and k varied with the tag's antenna configuration, tag implantation method, and posttagging recovery time. Our analytical approach can be used to gain insights across populations to better understand factors affecting the ability of fish to carry a transmitter.

  10. Swimming muscles power suction feeding in largemouth bass.

    PubMed

    Camp, Ariel L; Roberts, Thomas J; Brainerd, Elizabeth L

    2015-07-14

    Most aquatic vertebrates use suction to capture food, relying on rapid expansion of the mouth cavity to accelerate water and food into the mouth. In ray-finned fishes, mouth expansion is both fast and forceful, and therefore requires considerable power. However, the cranial muscles of these fishes are relatively small and may not be able to produce enough power for suction expansion. The axial swimming muscles of these fishes also attach to the feeding apparatus and have the potential to generate mouth expansion. Because of their large size, these axial muscles could contribute substantial power to suction feeding. To determine whether suction feeding is powered primarily by axial muscles, we measured the power required for suction expansion in largemouth bass and compared it to the power capacities of the axial and cranial muscles. Using X-ray reconstruction of moving morphology (XROMM), we generated 3D animations of the mouth skeleton and created a dynamic digital endocast to measure the rate of mouth volume expansion. This time-resolved expansion rate was combined with intraoral pressure recordings to calculate the instantaneous power required for suction feeding. Peak expansion powers for all but the weakest strikes far exceeded the maximum power capacity of the cranial muscles. The axial muscles did not merely contribute but were the primary source of suction expansion power and generated up to 95% of peak expansion power. The recruitment of axial muscle power may have been crucial for the evolution of high-power suction feeding in ray-finned fishes.

  11. Reduced swimming abilities in fast-growing transgenic common carp Cyprinus carpio associated with their morphological variations.

    PubMed

    Li, D; Hu, W; Wang, Y; Zhu, Z; Fu, C

    2009-01-01

    Critical swimming speeds (U(crit)) and morphological characters were compared between the F(4) generation of GH-transgenic common carp Cyprinus carpio and the non-transgenic controls. Transgenic fish displayed a mean absolute U(crit) value 22.3% lower than the controls. Principal component analysis identified variations in body shape, with transgenic fish having significantly deeper head, longer caudal length of the dorsal region, longer standard length (L(S)) and shallower body and caudal region, and shorter caudal length of the ventral region. Swimming speeds were related to the combination of deeper body and caudal region, longer caudal length of the ventral region, shallower head depth, shorter caudal length of dorsal region and L(S). These findings suggest that morphological variations which are poorly suited to produce maximum thrust and minimum drag in GH-transgenic C. carpio may be responsible for their lower swimming abilities in comparison with non-transgenic controls.

  12. Rainbow trout consume less oxygen in turbulence: the energetics of swimming behaviors at different speeds

    PubMed Central

    Taguchi, Masashige; Liao, James C.

    2011-01-01

    SUMMARY Measuring the rate of consumption of oxygen () during swimming reveals the energetics of fish locomotion. We show that rainbow trout have substantially different oxygen requirements for station holding depending on which hydrodynamic microhabitats they choose to occupy around a cylinder. We used intermittent flow respirometry to show that an energetics hierarchy, whereby certain behaviors are more energetically costly than others, exists both across behaviors at a fixed flow velocity and across speeds for a single behavior. At 3.5 L s–1 (L is total body length) entraining has the lowest , followed by Kármán gaiting, bow waking and then free stream swimming. As flow speed increases the costs associated with a particular behavior around the cylinder changes in unexpected ways compared with free stream swimming. At times, actually decreases as flow velocity increases. Entraining demands the least oxygen at 1.8 L s–1 and 3.5 L s–1, whereas bow waking requires the least oxygen at 5.0 L s–1. Consequently, a behavior at one speed may have a similar cost to another behavior at another speed. We directly confirm that fish Kármán gaiting in a vortex street gain an energetic advantage from vortices beyond the benefit of swimming in a velocity deficit. We propose that the ability to exploit velocity gradients as well as stabilization costs shape the complex patterns of oxygen consumption for behaviors around cylinders. Measuring for station holding in turbulent flows advances our attempts to develop ecologically relevant approaches to evaluating fish swimming performance. PMID:21490251

  13. Rainbow trout consume less oxygen in turbulence: the energetics of swimming behaviors at different speeds.

    PubMed

    Taguchi, Masashige; Liao, James C

    2011-05-01

    Measuring the rate of consumption of oxygen ( ) during swimming reveals the energetics of fish locomotion. We show that rainbow trout have substantially different oxygen requirements for station holding depending on which hydrodynamic microhabitats they choose to occupy around a cylinder. We used intermittent flow respirometry to show that an energetics hierarchy, whereby certain behaviors are more energetically costly than others, exists both across behaviors at a fixed flow velocity and across speeds for a single behavior. At 3.5 L s(-1) (L is total body length) entraining has the lowest , followed by Kármán gaiting, bow waking and then free stream swimming. As flow speed increases the costs associated with a particular behavior around the cylinder changes in unexpected ways compared with free stream swimming. At times, actually decreases as flow velocity increases. Entraining demands the least oxygen at 1.8 L s(-1) and 3.5 L s(-1), whereas bow waking requires the least oxygen at 5.0 L s(-1). Consequently, a behavior at one speed may have a similar cost to another behavior at another speed. We directly confirm that fish Kármán gaiting in a vortex street gain an energetic advantage from vortices beyond the benefit of swimming in a velocity deficit. We propose that the ability to exploit velocity gradients as well as stabilization costs shape the complex patterns of oxygen consumption for behaviors around cylinders. Measuring for station holding in turbulent flows advances our attempts to develop ecologically relevant approaches to evaluating fish swimming performance.

  14. Swimming impairment and acetylcholinesterase inhibition in zebrafish exposed to copper or chlorpyrifos separately, or as mixtures

    PubMed Central

    Tilton, Fred A.; Bammler, Theo K.; Gallagher, Evan P.

    2010-01-01

    Pesticides such as chlorpyrifos (CPF) and metals such as copper can impair swimming behavior in fish. However, the impact to swimming behavior from exposure to mixtures of neurotoxicants has received little attention. In the current study, we analyzed spontaneous swimming rates of adult zebrafish (Danio rerio) to investigate in vivo mixture interactions involving two chemical classes. Zebrafish were exposed to the neurotoxicants copper chloride (CuCl, 0.1 μM, 0.25 μM, 0.6 μM, or 6.3, 16, 40 ppb), chlorpyrifos (CPF, 0.1 μM, 0.25 μM, 0.6 μM, or 35, 88, 220 ppb) and binary mixtures for 24 hr to better understand the effects of Cu on CPF neurotoxicity. Exposure to CPF increased the number of animals undergoing freeze responses (an anti-predator behavior) and, at the highest CPF dose (0.6 μM), elicited a decrease in zebrafish swimming rates. Interestingly, the addition of Cu caused a reduction in the number of zebrafish in the CPF-exposure groups undergoing freeze responses. There was no evidence of additive or synergistic toxicity between Cu and CPF. Although muscle AChE activity was significantly reduced by CPF, there was a relatively poor relationship among muscle AChE concentrations and swimming behavior, suggesting non-muscle AChE mechanisms in the loss of swimming behavior. In summary, we have observed a modulating effect of Cu on CPF swimming impairment that appears to involve both AChE and non-AChE mechanisms. Our study supports the utility of zebrafish in understanding chemical mixture interactions and neurobehavioral injury. PMID:20692364

  15. Parental perceptions of toddler water safety, swimming ability and swimming lessons.

    PubMed

    Moran, K; Stanley, T

    2006-09-01

    The primary objective of the study was to examine parental perceptions on the role of toddler swimming ability and pre-school swimming lessons in drowning prevention. A self-administered questionnaire was used to obtain information on toddler water safety from parents (n = 882) whose 2 - 4-year-old toddlers were either attending early childhood centres (n = 327) or who were enrolled in swim schools (n = 555). Differences in attitudes between two groups of parents were measured by frequency, with Mann-Whitney U tests used to discern significant differences between groups. More swim school parents believed that: swimming was best taught at 2 years of age or less (42% vs. 29%); swimming lessons were the best way to prevent toddler drowning (57% vs. 47%); toddlers could learn to save themselves if they fell into water (43% vs. 33%); and that it was better to develop swimming ability rather than rely on adult supervision (35% vs. 30%). Many parents have an overly optimistic view of the role of swimming ability and pre-school swimming lessons in drowning prevention. This was especially so for parents with toddlers enrolled in lessons. Swim schools in particular need to counter parental misconceptions of the protective role of swimming and reiterate the importance of close adult supervision of toddlers around water.

  16. Teaching the Physically Handicapped to Swim.

    ERIC Educational Resources Information Center

    Anderson, William

    First principles of teaching swimming to the handicapped are reviewed; attention is given to children with cerebral palsy or muscular dystrophy, physical handicaps, blindness, and deafness. Swimming strokes, suggested exercises, group teaching, and a typical sequence of lessons and exercises are considered. Some case histories and a plan for a…

  17. Teaching Swimming--The Coach's Way.

    ERIC Educational Resources Information Center

    DeMarie, John

    1983-01-01

    Coaches of competitive swimmers use many types of equipment and teaching techniques that should also be available to physical educators who teach swimming. Equipment, such as goggles, hand paddles, swim benches, fins, kickboards, pace clocks, and pull buoys, and training methods used in conjunction with them, are discussed. (PP)

  18. A Training Program for Swimming Pool Operators.

    ERIC Educational Resources Information Center

    Pope, James R., Jr.; Mihalik, Brian J.

    1985-01-01

    In the United States today, there is a dramatic shortage of qualified public swimming pool operators. This article describes a training program initiated in South Carolina to serve the needs of everyone responsible for and involved in the safe operation and management of a public swimming pool. (MT)

  19. Swim pressure: stress generation in active matter.

    PubMed

    Takatori, S C; Yan, W; Brady, J F

    2014-07-11

    We discover a new contribution to the pressure (or stress) exerted by a suspension of self-propelled bodies. Through their self-motion, all active matter systems generate a unique swim pressure that is entirely athermal in origin. The origin of the swim pressure is based upon the notion that an active body would swim away in space unless confined by boundaries-this confinement pressure is precisely the swim pressure. Here we give the micromechanical basis for the swim stress and use this new perspective to study self-assembly and phase separation in active soft matter. The swim pressure gives rise to a nonequilibrium equation of state for active matter with pressure-volume phase diagrams that resemble a van der Waals loop from equilibrium gas-liquid coexistence. Theoretical predictions are corroborated by Brownian dynamics simulations. Our new swim stress perspective can help analyze and exploit a wide class of active soft matter, from swimming bacteria to catalytic nanobots to molecular motors that activate the cellular cytoskeleton.

  20. Swim Pressure: Stress Generation in Active Matter

    NASA Astrophysics Data System (ADS)

    Takatori, S. C.; Yan, W.; Brady, J. F.

    2014-07-01

    We discover a new contribution to the pressure (or stress) exerted by a suspension of self-propelled bodies. Through their self-motion, all active matter systems generate a unique swim pressure that is entirely athermal in origin. The origin of the swim pressure is based upon the notion that an active body would swim away in space unless confined by boundaries—this confinement pressure is precisely the swim pressure. Here we give the micromechanical basis for the swim stress and use this new perspective to study self-assembly and phase separation in active soft matter. The swim pressure gives rise to a nonequilibrium equation of state for active matter with pressure-volume phase diagrams that resemble a van der Waals loop from equilibrium gas-liquid coexistence. Theoretical predictions are corroborated by Brownian dynamics simulations. Our new swim stress perspective can help analyze and exploit a wide class of active soft matter, from swimming bacteria to catalytic nanobots to molecular motors that activate the cellular cytoskeleton.

  1. Assessment of Swimming in Physical Education

    ERIC Educational Resources Information Center

    Grosse, Susan J.

    2005-01-01

    This article presents an excerpt from the book "Assessment of Swimming in Physical Education" by Susan J. Grosse. In this excerpt, the different methods of assessment are discussed. Each type of assessment presented in the book has a place in swim curriculum. Assessments can measure form, skill application, knowledge, behavior, attitude, or…

  2. Swimming Motility Reduces Deposition to Silica Surfaces

    SciTech Connect

    Lu, Nanxi; Massoudieh, Arash; Liang, Xiaomeng; Hu, Dehong; Kamai, Tamir; Ginn, Timothy R.; Zilles, Julie L.; Nguyen, Thanh H.

    2015-01-01

    The role of swimming motility on bacterial transport and fate in porous media was evaluated. We present microscopic evidence showing that strong swimming motility reduces attachment of Azotobacter vinelandii cells to silica surfaces. Applying global and cluster statistical analyses to microscopic videos taken under non-flow conditions, wild type, flagellated A. vinelandii strain DJ showed strong swimming ability with an average speed of 13.1 μm/s, DJ77 showed impaired swimming averaged at 8.7 μm/s, and both the non-flagellated JZ52 and chemically treated DJ cells were non-motile. Quantitative analyses of trajectories observed at different distances above the collector of a radial stagnation point flow cell (RSPF) revealed that both swimming and non-swimming cells moved with the flow when at a distance of at least 20 μm from the collector surface. Near the surface, DJ cells showed both horizontal and vertical movement diverging them from reaching surfaces, while chemically treated DJ cells moved with the flow to reach surfaces, suggesting that strong swimming reduced attachment. In agreement with the RSPF results, the deposition rates obtained for two-dimensional multiple-collector micromodels were also lowest for DJ, while DJ77 and JZ52 showed similar values. Strong swimming specifically reduced deposition on the upstream surfaces of the micromodel collectors.

  3. Teaching the Physically Handicapped to Swim.

    ERIC Educational Resources Information Center

    Anderson, William

    First principles of teaching swimming to the handicapped are reviewed; attention is given to children with cerebral palsy or muscular dystrophy, physical handicaps, blindness, and deafness. Swimming strokes, suggested exercises, group teaching, and a typical sequence of lessons and exercises are considered. Some case histories and a plan for a…

  4. Basic Land Drills for Swimming Stroke Acquisition

    ERIC Educational Resources Information Center

    Zhang, Peng

    2014-01-01

    Teaching swimming strokes can be a challenging task in physical education. The purpose of the article is to introduce 12 on land drills that can be utilized to facilitate the learning of swimming strokes, including elementary back stroke, sidestroke, front crawl, back stroke, breaststroke, and butterfly. Each drill consists of four components…

  5. Assessment of Swimming in Physical Education

    ERIC Educational Resources Information Center

    Grosse, Susan J.

    2005-01-01

    This article presents an excerpt from the book "Assessment of Swimming in Physical Education" by Susan J. Grosse. In this excerpt, the different methods of assessment are discussed. Each type of assessment presented in the book has a place in swim curriculum. Assessments can measure form, skill application, knowledge, behavior, attitude, or…

  6. Teaching Swimming--The Coach's Way.

    ERIC Educational Resources Information Center

    DeMarie, John

    1983-01-01

    Coaches of competitive swimmers use many types of equipment and teaching techniques that should also be available to physical educators who teach swimming. Equipment, such as goggles, hand paddles, swim benches, fins, kickboards, pace clocks, and pull buoys, and training methods used in conjunction with them, are discussed. (PP)

  7. European Swimming Pool Designs Cross the Atlantic.

    ERIC Educational Resources Information Center

    Jaskulak, Neil

    1983-01-01

    Conventional swimming pools have been built with the needs of competitive swimmers in mind. Planners in several European countries have greatly increased swimming pool attendance by designing "leisure pools," based primarily on the needs and behavior of recreationists. Design of these pools and their equipment requirements are discussed.…

  8. European Swimming Pool Designs Cross the Atlantic.

    ERIC Educational Resources Information Center

    Jaskulak, Neil

    1983-01-01

    Conventional swimming pools have been built with the needs of competitive swimmers in mind. Planners in several European countries have greatly increased swimming pool attendance by designing "leisure pools," based primarily on the needs and behavior of recreationists. Design of these pools and their equipment requirements are discussed.…

  9. The turn of the sword: length increases male swimming costs in swordtails.

    PubMed

    Basolo, Alexandra L; Alcaraz, Guillermina

    2003-08-07

    Sexual selection via female mate choice can result in the evolution of elaborate male traits that incur substantial costs for males. Despite increased interest in how female mating preferences contribute to the evolution of male traits, few studies have directly quantified the locomotor costs of such traits. A sexually selected trait that could affect movement costs is the sword exhibited by male swordtail fishes: while longer swords may increase male mating success, they could negatively affect the hydrodynamic aspects of swimming activities. Here, we examine the energetic costs of the sword in Xiphophorus montezumae by experimentally manipulating sword length and measuring male aerobic metabolism during two types of activity, routine swimming and courtship swimming. Direct measurements of oxygen consumption indicate that males with longer swords expend more energy than males with shortened swords during both types of swimming. In addition, the sword increases the cost of male courtship. Thus, while sexual selection via female choice favours long swords, males with longer swords experience higher metabolic costs during swimming, suggesting that sexual and natural selection have opposing effects on sword evolution. This study demonstrates a hydrodynamic cost of a sexually selected trait. In addition, this study discriminates between the cost of a sexually selected trait used in courtship and other courtship costs.

  10. UNDULATORY SWIMMING: HOW TRAVELING WAVES ARE PRODUCED AND MODULATED IN SUNFISH (LEPOMIS GIBBOSUS)

    PubMed

    Long; Mchenry; Boetticher

    1994-07-01

    We have developed an experimental procedure in which the in situ locomotor muscles of dead fishes can be electrically stimulated to generate swimming motions. This procedure gives the experimenter control of muscle activation and the mechanical properties of the body. Using pumpkinseed sunfish, Lepomis gibbosus, we investigated the mechanics of undulatory swimming by comparing the swimming kinematics of live sunfish with the kinematics of dead sunfish made to swim using electrical stimulation. In electrically stimulated sunfish, undulatory waves can be produced by alternating left­right contractions of either all the axial muscle or just the precaudal axial muscle. As judged by changes in swimming speed, most of the locomotor power is generated precaudally and transmitted to the caudal fin by way of the skin and axial skeleton. The form of the traveling undulatory wave ­ as measured by tail-beat amplitude, propulsive wavelength and maximal caudal curvature ­ can be modulated by experimental control of the body's passive stiffness, which is a property of the skin, connective tissue and axial skeleton.

  11. Effect of temperature on swimming performance in juvenile southern catfish (Silurus meridionalis).

    PubMed

    Zeng, Ling-Qing; Cao, Zhen-Dong; Fu, Shi-Jian; Peng, Jiang-Lan; Wang, Yu-Xiang

    2009-06-01

    The critical swimming speed (U(crit), aerobic swimming performance) and endurance (anaerobic swimming performance) of juvenile southern catfish Silurus meridionalis Chen (9.8+/-0.1 cm body length and 8.09+/-0.17 g body mass, n=226) were investigated at 10, 15, 20, 25, and 30 degrees C. Both absolute U(crit) (cm s(-1)) and relative critical swimming speed (U(r), BL s(-1)) of juvenile southern catfish increased in the temperature zone from 10 to 25 degrees C (p<0.05) and plateaued between 25 and 30 degrees C. However, the relationship between endurance time (tested at 1.23, 1.59 and 1.79 U(r-max)) and temperature followed an approximate bell-shape curve as temperature rose (p<0.05). The optimum temperatures of maximal U(crit) (3.40 BL s(-1)) of juvenile southern catfish was 28.4 degrees C. But that of experimental fish's endurance which was tested at velocity of 1.59 and 1.79 U(r-max) was 23.2 degrees C. These results show that temperature has a significant effect on swimming performance in juvenile southern catfish.

  12. Stress response of lead-exposed rainbow trout (Oncorhynchus mykiss) during swimming performance and hypoxia challenges

    SciTech Connect

    Phillips, K.A. |; Caldwell, C.A.; Sandheinrich, M.B.

    1995-12-31

    Contaminants often invoke a stress response in aquatic organisms, and may compromise their capacity to respond to secondary stressors. This may reduce growth, reproduction and survival. The authors objectives were to assess the effects of lead and secondary stressors on hematology and blood chemistry of rainbow trout. After a 7 to 8-week aqueous exposure to Pb(100{micro}g/L), rainbow trout were challenged with forced swimming or hypoxia. Lead significantly reduced concentrations of 5-aminolevulinic acid dehydratase (ALAD), but not other constituents in the blood. Lead did not affect the swimming endurance of the fish. Hematocrit, mean cell hemoglobin content, and mean cell volume were significantly lower in Pb-exposed trout following the swimming challenge. Although hypoxia resulted in increased hematocrit and plasma glucose concentrations, there were no significant differences between the Pb and control groups. Hypoxia did not affect plasma chloride concentrations, although concentrations increased in Pb-exposed trout. There was no difference in lactic acid concentrations between Pb-exposed and control fish after forced swimming or hypoxia.

  13. Environmental estrogen(s) induced swimming behavioural alterations in adult zebrafish (Danio rerio).

    PubMed

    Goundadkar, Basavaraj B; Katti, Pancharatna

    2017-09-01

    The present study is an attempt to investigate the effects of long-term (75days) exposure to environmental estrogens (EE) on the swimming behaviour of zebrafish (Danio rerio). Adult zebrafish were exposed semi-statically to media containing commonly detected estrogenic water contaminants (EE2, DES and BPA) at a concentration (5ng/L) much lower than environmentally recorded levels. Time spent in swimming, surface preference, patterns and path of swimming were recorded (6mins) for each fish using two video cameras on day 15, 30 60 and 75. Video clips were analysed using a software program. Results indicate that chronic exposure to EE leads to increased body weight and size of females, reduced (P<0.05) swimming time, delay in latency, increased (P<0.05) immobility, erratic movements and freezing episodes. We conclude that estrogenic contamination of natural aquatic systems induces alterations in locomotor behaviour and associated physiological disturbances in inhabitant fish fauna. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Reductions in prolonged swimming capacity following freshwater colonization in multiple threespine stickleback populations.

    PubMed

    Dalziel, Anne C; Vines, Timothy H; Schulte, Patricia M

    2012-04-01

    We compared ancestral anadromous-marine and nonmigratory, stream-resident threespine stickleback (Gasterosteus aculeatus) populations to examine the outcome of relaxed selection on prolonged swimming performance. We reared marine and stream-resident fish from two locations in a common environment and found that both stream-resident populations had lower critical swimming speeds (U(crits) ) than marine populations. F1 hybrids from the two locations displayed significant differences in dominance, suggesting that the genetic basis for variation in U(crit) differs between locations. To determine which traits evolved in conjunction with, and may underlie, differences in performance capacity we measured a suite of traits known to affect prolonged swimming performance in fish. Although some candidate traits did not evolve (standard metabolic rate and two body shape traits), multiple morphological (pectoral fin size, shape, and four body shape measures) and physiological (maximum metabolic rate; MMR) traits evolved in the predicted direction in both stream-resident populations. However, data from F1 hybrids suggested that only one of these traits (MMR) had dominance effects similar to those of U(crit) in both locations. Overall, our data suggest that reductions in prolonged swimming performance were selected for in nonmigratory populations of threespine stickleback, and that decreases in MMR may mediate these reductions in performance.

  15. Magnetically Propelled Fish-Like Nanoswimmers.

    PubMed

    Li, Tianlong; Li, Jinxing; Zhang, Hongtao; Chang, Xiaocong; Song, Wenping; Hu, Yanan; Shao, Guangbin; Sandraz, Elodie; Zhang, Guangyu; Li, Longqiu; Wang, Joseph

    2016-11-01

    The swimming locomotion of fish involves a complex interplay between a deformable body and induced flow in the surrounding fluid. While innovative robotic devices, inspired by physicomechanical designs evolved in fish, have been created for underwater propulsion of large swimmers, scaling such powerful locomotion into micro-/nanoscale propulsion remains challenging. Here, a magnetically propelled fish-like artificial nanoswimmer is demonstrated that emulates the body and caudal fin propulsion swimming mechanism displayed by fish. To mimic the deformable fish body for periodic shape changes, template-electrosynthesized multisegment nanowire swimmers are used to construct the artificial nanofishes (diameter 200 nm; length 4.8 μm). The resulting nanofish consists a gold segment as the head, two nickel segments as the body, and one gold segment as the caudal fin, with three flexible porous silver hinges linking each segment. Under an oscillating magnetic field, the propulsive nickel elements bend the body and caudal fin periodically to generate travelling-wave motions with speeds exceeding 30 μm s(-1) . The propulsion dynamics is studied theoretically using the immersed boundary method. Such body-deformable nanofishes exhibit a high swimming efficiency and can serve as promising biomimetic nanorobotic devices for nanoscale biomedical applications. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Shigellosis outbreak associated with swimming.

    PubMed Central

    Makintubee, S; Mallonee, J; Istre, G R

    1987-01-01

    In June 1982, an outbreak of gastrointestinal illness caused by Shigella sonnei occurred among residents of two counties in Oklahoma. A case-control study of cases and age and sex-matched controls showed an association with attendance at a southern Oklahoma lake (14/17 cases vs 3/17 controls, matched pair odds ratio [OR] 9/0, confidence interval [CI] 2.4-infinity). A survey of 85 persons who had visited the lake area showed that persons who had swum were more likely to have been ill with a gastrointestinal illness (50 per cent) than persons who had not swum (0 per cent); among those who had swum, illness was more frequent among those who reported having water in their mouths while swimming (62 per cent) than those who did not (19 per cent) (OR = 6.9, 95% CI = 2.2-21.5). No further primary lake-associated cases had onset of symptoms beyond two days of closing the reservoir. Swimming should be considered as a potential source of enteric infections. PMID:3541651

  17. Choreographed swimming of copepod nauplii

    PubMed Central

    Takagi, Daisuke; Hartline, Daniel K.

    2015-01-01

    Small metazoan paddlers, such as crustacean larvae (nauplii), are abundant, ecologically important and active swimmers, which depend on exploiting viscous forces for locomotion. The physics of micropaddling at low Reynolds number was investigated using a model of swimming based on slender-body theory for Stokes flow. Locomotion of nauplii of the copepod Bestiolina similis was quantified from high-speed video images to obtain precise measurements of appendage movements and the resulting displacement of the body. The kinematic and morphological data served as inputs to the model, which predicted the displacement in good agreement with observations. The results of interest did not depend sensitively on the parameters within the error of measurement. Model tests revealed that the commonly attributed mechanism of ‘feathering’ appendages during return strokes accounts for only part of the displacement. As important for effective paddling at low Reynolds number is the ability to generate a metachronal sequence of power strokes in combination with synchronous return strokes of appendages. The effect of feathering together with a synchronous return stroke is greater than the sum of each factor individually. The model serves as a foundation for future exploration of micropaddlers swimming at intermediate Reynolds number where both viscous and inertial forces are important. PMID:26490629

  18. How Giardia Swim and Divide

    PubMed Central

    Ghosh, Sudip; Frisardi, Marta; Rogers, Rick; Samuelson, John

    2001-01-01

    To determine how binuclear giardia swim, we used video microscopy to observe trophozoites of Giardia intestinalis, which were labeled with an amino-specific Alexa Fluor dye that highlighted the flagella and adherence disc. Giardia swam forward by means of the synchronous beating of anterior, posterolateral, and ventral flagella in the plane of the ventral disc, while caudal flagella swam in a plane perpendicular to the disc. Giardia turned in the plane of the disc by means of a rudder-like motion of its tail, which was constant rather than beating. To determine how giardia divide, we used three-dimensional confocal microscopy, the same surface label, nuclear stains, and antitubulin antibodies. Giardia divided with mirror-image symmetry in the plane of the adherence disc, so that the right nucleus of the mother became the left nucleus of the daughter. Pairs of nuclei were tethered together by microtubules which surrounded nuclei and prevented mother or daughter giardia from receiving two copies of the same nucleus. New adherence discs formed upon a spiral backbone of microtubules, which had a clockwise rotation when viewed from the ventral surface. These dynamic observations of the parasite begin to reveal how giardia swim and divide. PMID:11705969

  19. Winter swimming improves general well-being.

    PubMed

    Huttunen, Pirkko; Kokko, Leena; Ylijukuri, Virpi

    2004-05-01

    This study deals with the effects of regular winter swimming on the mood of the swimmers. Profile of Mood State (POMS) and OIRE questionnaires were completed before (October) and after (January) the four-month winter swimming period. In the beginning, there were no significant differences in the mood states and subjective feelings between the swimmers and the controls. The swimmers had more diseases (about 50%) diagnosed by a physician. Tension, fatigue, memory and mood negative state points in the swimmers significantly decreased with the duration of the swimming period. After four months, the swimmers felt themselves to be more energetic, active and brisk than the controls. Vigour-activity scores were significantly greater (p < 0.05). All swimmers who suffered from rheumatism, fibromyalgia, or asthma, reported that winter swimming had relieved pains. Improvement of general well-being is thus a benefit induced by regular winter swimming.

  20. Undulatory swimming in non-Newtonian fluids

    NASA Astrophysics Data System (ADS)

    Ardekani, Arezoo; Li, Gaojin

    2015-11-01

    Microorganisms often swim in complex fluids exhibiting both elasticity and shear-thinning viscosity. The motion of low Reynolds number swimmers in complex fluids is important for better understanding the migration of sperms and formation of bacterial biofilms. In this work, we numerically investigate the effects of non-Newtonian fluid properties, including shear-thinning and elasticity, on the undulatory locomotion. Our results show that elasticity hinders the swimming speed, but a shear-thinning viscosity in the absence of elasticity enhances the speed. The combination of the two effects hinders the swimming speed. The swimming boost in a shear-thinning fluid occurs even for an infinitely long flagellum. The swimming speed has a maximum, whose value depends on the flagellum oscillation amplitude and fluid rheological properties. The power consumption, on the other hand, follows a universal scaling law. This work is supported by NSF CBET-1445955 and Indiana CTSI TR001108.