scholarly journals Decoding the Relationships between Body Shape, Tail Beat Frequency, and Stability for Swimming Fish

Fluids ◽  
2020 ◽  
Vol 5 (4) ◽  
pp. 215
Author(s):  
Alexander P. Hoover ◽  
Eric Tytell

As fish swim through a fluid environment, they must actively use their fins in concert to stabilize their motion and have a robust form of locomotion. However, there is little knowledge of how these forces act on the fish body. In this study, we employ a 3D immersed boundary model to decode the relationship between roll, pitch, and yaw of the fish body and the driving forces acting on flexible fish bodies. Using bluegill sunfish as our representative geometry, we first examine the role of an actuating torque on the stability of the fish model, with a torque applied at the head of the unconstrained fish body. The resulting kinematics is a product of the passive elasticity, fluid forces, and driving torque. We then examine a constrained model to understand the role that fin geometry, body elasticity, and frequency play on the range of corrective forces acting on the fish. We find non-monotonic behavior with respect to frequency, suggesting that the effective flexibility of the fins play an important role in the swimming performance.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yi Zhu ◽  
Fang-Bao Tian ◽  
John Young ◽  
James C. Liao ◽  
Joseph C. S. Lai

AbstractFish adaption behaviors in complex environments are of great importance in improving the performance of underwater vehicles. This work presents a numerical study of the adaption behaviors of self-propelled fish in complex environments by developing a numerical framework of deep learning and immersed boundary–lattice Boltzmann method (IB–LBM). In this framework, the fish swimming in a viscous incompressible flow is simulated with an IB–LBM which is validated by conducting two benchmark problems including a uniform flow over a stationary cylinder and a self-propelled anguilliform swimming in a quiescent flow. Furthermore, a deep recurrent Q-network (DRQN) is incorporated with the IB–LBM to train the fish model to adapt its motion to optimally achieve a specific task, such as prey capture, rheotaxis and Kármán gaiting. Compared to existing learning models for fish, this work incorporates the fish position, velocity and acceleration into the state space in the DRQN; and it considers the amplitude and frequency action spaces as well as the historical effects. This framework makes use of the high computational efficiency of the IB–LBM which is of crucial importance for the effective coupling with learning algorithms. Applications of the proposed numerical framework in point-to-point swimming in quiescent flow and position holding both in a uniform stream and a Kármán vortex street demonstrate the strategies used to adapt to different situations.


1991 ◽  
Vol 156 (1) ◽  
pp. 63-80 ◽  
Author(s):  
C. Shingyoji ◽  
I. R. Gibbons ◽  
A. Murakami ◽  
K. Takahashi

The heads of live spermatozoa of the sea urchin Hemicentrotus pulcherrimus were held by suction in the tip of a micropipette mounted on a piezoelectric device and vibrated either laterally or axially with respect to the head axis. Within certain ranges of frequency and amplitude, lateral vibration of the pipette brought about a stable rhythmic beating of the flagella in the plane of vibration, with the beat frequency synchronized to the frequency of vibration [Gibbons et al. (1987), Nature 325, 351–352]. The sperm flagella, with an average natural beat frequency of 48 Hz, showed stable beating synchronized to the pipette vibration over a range of 35–90 Hz when the amplitude of vibration was about 20 microns or greater. Vibration frequencies below this range caused instability of the beat plane, often associated with irregularities in beat frequency. Frequencies above about 90 Hz caused irregular asymmetrical flagellar beating with a marked decrease in amplitude of the propagated bends and a skewing of the flagellar axis towards one side; the flagella often stopped in a cane shape. In flagella that were beating stably under imposed vibration, the wavelength was reduced at higher frequencies and increased at lower frequencies. When the beat frequency was equal to or lower than the natural beat frequency, the apparent time-averaged sliding velocity of axonemal microtubules, obtained as twice the product of frequency and bend angle, decreased with beat frequency in both the proximal and distal regions of the flagella. However, at vibration frequencies above the natural beat frequency, the sliding velocity increased with frequency only in the proximal region of the flagellum and remained essentially unchanged in more distal regions. This apparent limit to the velocity of sliding in the distal region may represent an inherent limit in the intrinsic velocity of active sliding, while the faster sliding observed in the proximal region may be a result of passive sliding or elastic distortion of the microtubules induced by the additional energy supplied by the vibrating pipette. Axial vibration with frequencies either close to or twice the natural beat frequency induced cyclic changes in the waveform, compressing and expanding the bends in the proximal region, but did not affect bends in the distal region or alter the beat frequency.


1993 ◽  
Vol 178 (1) ◽  
pp. 97-108 ◽  
Author(s):  
P. W. Webb

Kinematics and steady swimming performance were recorded for steelhead trout (approximately 12.2 cm in total length) swimming in channels 4.5, 3 and 1.6 cm wide in the centre of a flume 15 cm wide. Channel walls were solid or porous. Tail-beat depth and the length of the propulsive wave were not affected by spacing of either solid or porous walls. The product of tail-beat frequency, F, and amplitude, H, was related to swimming speed, u, and to harmonic mean distance of the tail from the wall, z. For solid walls: FH = 1.01(+/−0.31)u0.67(+/−0.09)z(0.12+/−0.02) and for grid walls: FH = 0.873(+/−0.302)u0.74(+/−0.08)z0.064(+/−0.024), where +/−2 s.e. are shown for regression coefficients. Thus, rates of working were smaller for fish swimming between solid walls, but the reduction due to wall effects decreased with increasing swimming speed. Porous grid walls had less effect on kinematics, except at low swimming speeds. Spacing of solid walls did not affect maximum tail-beat frequency, but maximum tail-beat amplitude decreased with smaller wall widths. Maximum tail-beat amplitude similarly decreased with spacing between grid walls, but maximum tail-beat frequency increased. Walls also reduced maximum swimming speed. Wall effects have not been adequately taken into account in most studies of fish swimming in flumes and fish wheels.


2021 ◽  
Author(s):  
Junshi Wang ◽  
Vadim Pavlov ◽  
Zhipeng Lou ◽  
Haibo Dong

Abstract Dolphins are known for their outstanding swimming performance. However, the difference in flow physics at different speeds remains elusive. In this work, the underlying mechanisms of dolphin swimming at three speeds, 2 m/s, 5 m/s, and 8 m/s, are explored using a combined experimental and numerical approach. Using the scanned CAD model of the Atlantic white-sided dolphin (Lagenorhynchus acutus) and virtual skeleton-based surface reconstruction method, a three-dimensional high-fidelity computational model is obtained with time-varying kinematics. A sharp-interface immersed-boundary-method (IBM) based direct numerical simulation (DNS) solver is employed to calculate the corresponding thrust production, wake structure, and surface pressure at different swimming speeds. It is found that the fluke keeps its effective angle of attack at high values for about 60% of each stroke. The total pressure force coefficient along the x-axis converges as the speed increase. The flow and surface pressure analysis both show considerable differences between lower (2 m/s) and higher (5 m/s and 8 m/s) speeds. The results from this work help to bring new insight into understanding the force generation mechanisms of the highly efficient dolphin swimming and offer potential suggestions to the future designs of unmanned underwater vehicles.


2017 ◽  
Vol 826 ◽  
pp. 996-1033 ◽  
Author(s):  
Qinmin Zheng ◽  
Md. Mahbub Alam

An investigation on the flow around three side-by-side square prisms can provide a better understanding of complicated flow physics associated with multiple, closely spaced structures in which more than one gap flow is involved. In this paper, the flow around three side-by-side square prisms at a Reynolds number $Re=150$ is studied systematically at $L/W=1.1{-}9.0$, where $L$ is the prism centre-to-centre spacing and $W$ is the prism width. Five distinct flow structures and their ranges are identified, viz. base-bleed flow ($L/W<1.4$), flip-flopping flow $(1.4<L/W<2.1)$, symmetrically biased beat flow $(2.1<L/W<2.6)$, non-biased beat flow $(2.6<L/W<7.25)$ and weak interaction flow $(7.25<L/W<9.0)$. Physical aspects of each flow regime, such as vortex structures, vortex dynamics, gap-flow behaviours, shedding frequencies and fluid forces, are discussed in detail. A secondary (beat) frequency other than the Strouhal frequency (primary frequency) is observed in the symmetrically biased and non-biased beat flows, associated with the beat-like modulation in $C_{L}$-peak or amplitude, where $C_{L}$ is the lift force coefficient. Here we reveal the generic and intrinsic origin of the secondary frequency, establishing its connections with the phase lag between the two shear-layer sheddings from the two sides of a gap. When the two sheddings are in phase, no viscous force acts at the interface (i.e. at the centreline of the gap) of the two sheddings, resulting in the largest fluctuations in streamwise momentum, streamwise velocity and pressure; the maximum $C_{L}$ amplitude thus features the in-phase shedding. Conversely, when the two sheddings are antiphase, a viscous force exists at the interface of the two sheddings and restricts the momentum fluctuation through the gap, yielding a minimum $C_{L}$ amplitude. When the phase relationship between the two sheddings changes from in phase to antiphase, the extra viscous force acting at the interface becomes larger and causes the $C_{L}$ amplitude to change from a maximum to a minimum.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Fuxing Li ◽  
Hao Liu ◽  
Menglei Li ◽  
Jun Guo ◽  
Xinjian Lu ◽  
...  

Inertia force is an important factor for operation stability and stamping precision of high-speed punch; adjusting drive torque of high-speed punch can realize effective control of inertia force. In this paper, a kind of 600 KN multilink high-speed punch inertia force balancing mechanism was designed. The calculation model of ideal inertia force was proposed based on conservation of energy and numerical analysis method. In addition, the calculation model of ideal driving torque were analyzed, simplified, and corrected by using numerical calculation and simulation methods, which solved the problem of controlling inertia force from the perspective of driving torque and realized the stability strategy planning of high-speed multilink punch press. Finally, the proposed ideal driving torque calculation model was simulated and verified by ADAMAS and bottom-dead-point accuracy test was carried out.


Author(s):  
Wei Ge ◽  
Ning Yang ◽  
Wei Wang ◽  
Jinghai Li

The drag interaction between gas and solids not only acts as a driving force for solids in gas-solids flows but also plays as a major role in the dissipation of the energy due to drag losses. This leads to enormous complexities as these drag terms are highly non-linear and multiscale in nature because of the variations in solids spatio-temporal distribution. This chapter provides an overview of this important aspect of the hydrodynamic interactions between the gas and solids and the role of spatio-temporal heterogeneities on the quantification of this drag force. In particular, a model is presented which introduces a mesoscale description into two-fluid models for gas-solids flows. This description is formulated in terms of the stability of gas-solids suspension. The stability condition is, in turn, posed as a minimization problem where the competing factors are the energy consumption required to suspend and transport the solids and their gravitational potential energy. However, the lack of scale-separation leads to many uncertainties in quantifying mesoscale structures. The authors have incorporated this model into computational fluid dynamics (CFD) simulations which have shown improvements over traditional drag models. Fully resolved simulations, such as those mentioned in this chapter and the subject of a later chapter on Immersed Boundary Methods, can be used to obtain additional information about these mesoscale structures. This can be used to formulate better constitutive equations for continuum models.


Author(s):  
Katsuhisa Fujita ◽  
Atsuhiko Shintani ◽  
Koji Yoshioka ◽  
Kouhei Okuno ◽  
Hiroaki Tanaka ◽  
...  

Recently, in many areas such as computers and information equipments etc., the fluid journal bearings are required to rotate at higher speed. To satisfy this requirement, the strictly stability analysis of the journal is indispensable. In this paper, we investigate the stability analysis of the dynamic behavior of the fluid plain journal bearing with an incompressible fluid considering the nonlinear terms of fluid forces. The stability analysis is examined by the numerical simulations on each model of a rigid rotor and a flexible rotor. The stable regions by nonlinear analysis are compared with the regions by classical linear analysis. Performing the nonlinear simulation analysis, it becomes clear that there is rather a stable region which amplitude does not grow up abruptly, and this phenomenon can not only be pointed out, but also is judged to be unstable by linear stable analysis. Finally, the experiment using actual bearings is performed and compared with the numerical results.


Author(s):  
Toma´sˇ Gedeon ◽  
Jeff J. Heys ◽  
B. C. Knott ◽  
Jonas Mulder-Rosi

Many insects are able to sense their surrounding fluid environment through induced motion of their filiform hairs. The mechanism by which the insect can sense a wide range of input signals using the canopy of filiform hairs of different length and orientation is of great interest. Most of the previous filiform hair models have focused on a single, rigid hair in an idealized air field. We have developed [1] a model for a canopy of filiform hairs that are mechanically coupled to the surrounding air. The model equations are based on the penalty immersed boundary method. The key difference between the penalty immersed boundary method and the traditional immersed boundary method is the addition of forces to account for density differences between the immersed solid (the filiform hairs) and the surrounding fluid (air). In this work we validate the model by comparing the model predictions to experimental results on cricket Acheta domestica cercal system.


Fluids ◽  
2019 ◽  
Vol 4 (3) ◽  
pp. 169 ◽  
Author(s):  
Jason G. Miles ◽  
Nicholas A. Battista

Jellyfish are majestic, energy-efficient, and one of the oldest species that inhabit the oceans. It is perhaps the second item, their efficiency, that has captivated scientists for decades into investigating their locomotive behavior. Yet, no one has specifically explored the role that their tentacles and oral arms may have on their potential swimming performance. We perform comparative in silico experiments to study how tentacle/oral arm number, length, placement, and density affect forward swimming speeds, cost of transport, and fluid mixing. An open source implementation of the immersed boundary method was used (IB2d) to solve the fully coupled fluid–structure interaction problem of an idealized flexible jellyfish bell with poroelastic tentacles/oral arms in a viscous, incompressible fluid. Overall tentacles/oral arms inhibit forward swimming speeds, by appearing to suppress vortex formation. Nonlinear relationships between length and fluid scale (Reynolds Number) as well as tentacle/oral arm number, density, and placement are observed, illustrating that small changes in morphology could result in significant decreases in swimming speeds, in some cases by upwards of 80–90% between cases with or without tentacles/oral arms.


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