Next Article in Journal
Experimental Investigation of Finite Aspect Ratio Cylindrical Bodies for Accelerated Wind Applications
Next Article in Special Issue
Suction Flows Generated by the Carnivorous Bladderwort Utricularia—Comparing Experiments with Mechanical and Mathematical Models
Previous Article in Journal
Numerical Analysis of Magnetohydrodynamic Flows
Previous Article in Special Issue
Fluid Dynamics of Ballistic Strategies in Nematocyst Firing
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Metachronal Swimming with Rigid Arms near Boundaries

1
Department of Mechanical Engineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA
2
Department of Mathematics, University of Hawaii at Manoa, Honolulu, HI 96822, USA
*
Author to whom correspondence should be addressed.
Fluids 2020, 5(1), 24; https://doi.org/10.3390/fluids5010024
Submission received: 6 December 2019 / Revised: 17 January 2020 / Accepted: 10 February 2020 / Published: 14 February 2020
(This article belongs to the Special Issue Advances in Biological Flows and Biomimetics)

Abstract

:
Various organisms such as crustaceans use their appendages for locomotion. If they are close to a confining boundary then viscous as opposed to inertial effects can play a central role in governing the dynamics. To study the minimal ingredients needed for swimming without inertia, we built an experimental system featuring a robot equipped with a pair of rigid slender arms with negligible inertia. Our results show that directing the arms to oscillate about the same time-averaged orientation produces no net displacement of the robot each cycle, regardless of any phase delay between the oscillating arms. The robot is able to swim if the arms oscillate asynchronously around distinct orientations. The measured displacement over time matches well with a mathematical model based on slender-body theory for Stokes flow. Near a confining boundary, the robot with no net displacement every cycle showed similar behavior, while the swimming robot increased in speed closer to the boundary.

1. Introduction

A diversity of organisms rely on the coordination of multiple appendages for locomotion. Examples include various crustaceans such as copepods [1], remipedes [2], krill [3,4], crabs [5], and lobsters [6,7]. There is commonly a phase delay between the oscillation of adjacent appendages, which collectively produce a rhythm referred to as a metachronal wave [8,9,10]. The metachronal wave typically travels along the body of the swimmer in the direction of locomotion [4,6,11]. The swimming performance depends on numerous factors, which include the shape, amplitude, phase, and number of oscillating appendages [4,10,12,13].
Here we consider the basic physical ingredients needed to swim with rigid appendages through a viscous fluid with small inertia. This is partly inspired by the locomotion of microscopic crustaceans operating in a physical regime of low Reynolds number. In this physical regime, locomotion requires cycles of non-reciprocal motion in order to overcome the dominant effects of viscosity [14]. A common strategy adopted by microscopic organisms is to rely on many flexible flagella and cilia beating collectively in a metachronal rhythm [15,16], though other organisms such as larval copepods have relatively stiff and smaller number of appendages. Our previous experiments showed that two rigid arms are sufficient for generating flow, provided that there is a phase difference between the oscillating arms [17]. However, the arms were fixed in place and not mobile. There is a fundamental difference between the fluid flow fields around fixed and mobile arms because the fixed arms are subjected to a net force, while the mobile arms can be force-free in the limit of negligible inertia. Flow generation does not necessarily imply locomotion. Thus, further research is needed to understand the minimal ingredients for locomotion.
Here we report a series of experiments designed to study the motion of a simple robot with a pair of rigid arms. The arms are dipped in silicone oil, while the rest of the robot is placed on a linear air track so that it is able to move freely along the horizontal track. The position of the robot was tracked over time and compared with a previously developed model based on the slender-body theory for Stokes flow [12]. Although the theory neglects the effects of inertia and confinement which are present in the experiments, the predictions match reasonably well with the experimental data. Our study offers novel insight into the significance of directing the arms to oscillate about distinct orientations for propulsion. This may have some implications for the morphology of tiny crustaceans such as larval copepods, which have three pairs of legs radiating out from their small rounded body.

2. Materials and Methods

The experimental system featured a robot equipped with a pair of rigid arms that were immersed in a tank of silicone oil as sketched in Figure 1a. The arms were each actuated by a servo motor (TowerPro SG90) and labeled as Arm 1 and Arm 2 (Figure 1b). Each arm was 3D printed with Acrylonitrile Butadiene Styrene (ABS) plastic and shaped into a rigid rod of length L = 40 mm and diameter 2 mm. The robot was designed to glide on a virtually frictionless surface of an air track system (Eisco PH0362A) such that it could translate freely along the linear track. The ridge-shaped track prevented the robot from rocking or veering off the horizontal track. The air track was fixed onto two adjustable platform stands (Wisamic 8“ × 8“ Lab Jack) to raise or lower the height of the robot as needed. The arms were dipped to a depth of H = 30 mm below the surface of a large cylindrical bath of silicone oil with total depth 190 mm, diameter 300 mm, and kinematic viscosity ν = 12,500 mm2/s at room temperature.
The robotic arms were controlled by a microcontroller (ATmega328P) and a wireless module (XBee XB24CZ7WIT-004 and communicated using XCTU) powered by a 9 V battery. The two arms were programmed to pivot around two axes separated by a distance D = 23 mm. This separation distance needed to be sufficiently large to avoid collisions and hydrodynamic interactions, which were neglected in our theoretical analysis. The horizontal directions from one pivot along and across the line to the other pivot are denoted by x and y axes, respectively. Each arm was set to oscillate periodically over time t such that the angle θ i to the x axis changed according to
θ 1 ( t ) = θ 1 ¯ A sin ( ω t ) ,
θ 2 ( t ) = θ 2 ¯ A sin ( ω t ϕ ) ,
where A is the amplitude, ω is the angular speed, ϕ is the phase difference, and θ i ¯ is the median angle of the ith arm. In this study we varied ϕ and θ i ¯ in three separate cases (Table 1). In Case 1, ϕ is set to zero, meaning that the two arms move synchronously. In Cases 2 and 3, the two arms move asynchronously with a phase difference of π / 2 . In Case 2, the two arms have distinct median angles, whereas in Case 3, the median angles are identical. The amplitude was fixed to A = 20 ° and the angular frequency was fixed to ω = 1.484 rad/s, corresponding to an oscillation period of T = 2 π / ω = 4.23 s. The Reynolds number of the fluid flow was computed to be R e = ω L 2 / ν = 0.19 , which is much smaller than 1. Thus the inertia of the oil is expected to play a minor role in the experiments. The inertia of the robot may have a more significant effect because a large proportion of the mobile body is not immersed in the oil. The combined mass of the mobile robot on the air track was measured to be 255 g.
To study the effects of a nearby boundary on the dynamics of the robot, we performed the three cases with a smaller gap h between the floor and the tips of the arms (Figure 2a). This was achieved by adjusting both the height of the air track and the depth of the silicone oil in a shallower rectangular tank with dimensions of 610 mm × 457 mm × 76 mm. To introduce additional confinement effects, we inserted two transparent walls perpendicular to the floor at a distance w away from the arms, as sketched in Figure 2b.
The air track was levelled carefully each time the distance h to the floor was varied. First, we ensured that the robot, with its arms powered off, remained stationary on the track with the air pump turned on. If the track were not sufficiently level, the robot would have drifted down the track due to gravity. Second, we verified that the robot, with its arms actuated in Case 1, showed the same behavior moving in one direction as in the opposite direction, resulting in no net displacement every cycle. The two jacks were adjusted as needed until we observed the expected behavior on a horizontal track. Once the air track was calibrated, each run was recorded for a minute, which corresponds to approximately 14 cycles. The position of the robot was recorded at 30 frames per second (Sony Alpha A6000 camera) and tracked using an open source tracking software (Tracker). The data were analyzed and plotted in MATLAB.

3. Results

The displacement of the robot changes with time as shown in Figure 3. In Case 1 with the arms moving synchronously, the body moves back and forth with minimal displacement at the end of each cycle. In Case 2 with the arms moving asynchronously, the body moves back and forth but drifts slowly in one direction, resulting in locomotion. In Case 3, even though the arms are moving asynchronously, the body again shows minimal displacement after each cycle. There are some variations in the net displacement every cycle, possibly caused by time-varying forces on the robot. For example, the lift force from the air track may fluctuate slightly over time because of unsteady air flow from the discrete set of holes on the air track, though the exact origin of the fluctuations is unclear. Nevertheless, the variations are small in magnitude and showed no systematic changes in displacement in Cases 1 and 3 as in Case 2. This shows that the key parameter for swimming with rigid arms is not only the phase difference but also the orientation of the arms.
The orientation angles of the arms and the displacement of the robot within one cycle are shown in Figure 4. 14 cycles were averaged and the mean and standard deviation at each time step are plotted. In Case 1, when the arms reverse the direction of motion at the time points of 0.25 and 0.75 into the periodic cycle, the robot still has momentum and does not immediately reverse its motion. There is a short time lag when the robot reverses direction due to small inertial effects. As a result, the robot does not return to its original position after half the periodic cycle. Nevertheless, after a full periodic cycle, there is minimal displacement in Case 1 ( 0.1 ± 0.4 mm) and Case 3 ( 0.1 ± 0.4 mm) compared to Case 2 ( 1.2 ± 0.3 mm). The displacement curves in Cases 2 and 3 are similar at the beginning but differ toward the end of the cycle.
The effect of a rigid boundary was investigated by placing the arms at a closer distance h to the floor (Figure 2a). In Case 1 with synchronous arms, the displacement of the robot over time is almost identical near the floor ( h = 5 mm) and far away from the floor ( h = 160 mm), as shown in Figure 5. In Case 2, interestingly, the net displacement per cycle increases from 1.2 to 1.8 mm as the robot is placed closer to the floor. There is no noticeable difference in the displacement of the robot in Case 3 closer to the floor.
The net displacements per cycle at different distances h are shown in Figure 6. As h decreases, the net displacement per cycle remains around zero in Case 1 and Case 3. In Case 2, the net displacement per cycle increases slightly from 1.2 mm at h = 160 mm to 1.4 mm at h = 30 mm. Then it increases more significantly to 1.8 mm at h = 5 mm. The robot in Case 2 is able to swim at higher speed as it gets closer to the floor.
We introduced additional confinement effects by inserting two vertical walls on both sides of the arms at a distance w = 5 mm away (Figure 2b). There was no noticeable difference in the displacement of the robot in Cases 1 and 3, as shown in Figure 5 and Figure 6. In Case 2, the net displacement per cycle further increased to 2.1 mm after introducing the walls in addition to the floor around the arms.

4. Discussion

In our experimental system, there is an air-oil interface above the rigid arms. But the flow field around the two arms is equivalent to that around four arms completely immersed in silicone oil, which is obtained by constructing a reflected image as sketched in Figure 7. The original set of two arms and the surrounding flow of oil can be readily reflected across the air-oil interface as long as the interface remains flat, an approximation that is expected to be valid when the flow generated by the arms is sufficiently weak. The equivalence arises because the stress-free boundary condition at the flat interface is satisfied automatically by the symmetric flow at the plane of reflective symmetry.
We analyze and interpret our experimental results using a mathematical model of a swimmer having rigid slender legs [12]. The model neglects inertia and confinement effects. For a body of negligible size equipped with two pairs of arms, the model predicts that the velocity of the body at any instant is given by
V = θ 1 ˙ sin θ 1 + θ 2 ˙ sin θ 2 2 + sin 2 θ 1 + sin 2 θ 2
in units of arm length L per period T. Equation (3) is integrated numerically to obtain the displacement over time. The predicted displacement in the model is compared with the experimental data in Figure 8. Overall, there is very good agreement between the predicted and measured data when the robot is far away from the floor and walls.
The model also predicts that, if the orientation angles of the arms oscillate with a small amplitude A in radians, the expected displacement every cycle is given by [12]
Δ 2 π L A 2 ( cos θ 2 ¯ cos θ 1 ¯ ) sin θ 1 ¯ sin θ 2 ¯ sin ϕ ( 2 + sin 2 θ 1 ¯ + sin 2 θ 2 ¯ ) 2 .
The expected displacement is proportional to the square of the amplitude A and to sin ϕ . Changing the sign of the phase difference ϕ changes the sign of Δ , meaning that the swimming direction depends on the metachronal wave of the oscillating arms. Interestingly, the swimming direction depends also on the two median angles θ 1 ¯ and θ 2 ¯ . Figure 9 shows the expected displacement every cycle as a function of the two median angles, with the phase difference fixed at ϕ = π / 2 and the amplitude set at A = 20 ° . If the arms have the same median angle, θ 1 ¯ = θ 2 ¯ , then we expect no displacement every cycle, which is consistent with our observations. If the arms oscillate asynchronously around two distinct orientations, then the body is expected to swim in general. The swimming direction reverses if the two median angles are switched. The displacement is maximized when the two median angles are α and π α radians, where α = arcsin ( 5 17 ) / 2 is about 41.5 degrees, obtained from setting the derivative of Equation (4) to zero.
The predicted net displacement per cycle matches very well when the arms are far away from the floor ( h = 160 mm) but begins to deviate only in Case 2 as the arms get closer to the floor shown in Figure 6. Interestingly, the swimming speed increases as the robot arms are confined further by the floor and the walls. Similar results have been previously reported with different type of swimmers in confinement [7,18,19,20,21,22,23,24,25]. For instance, a microswimmer modeled as an infinite waving sheet is able to swim faster near parallel walls with an increase in the rate of working by the sheet [18]. The effect of boundaries in our experiments could be partly explained by adopting the method of images in theory, a technique for imposing the no-slip condition on the boundary by introducing a suitable combination of Stokeslets across the boundary. To a first approximation, the flow around a single robot at a distance h to a boundary is equivalent to that around a pair of robots, one corresponding to a mirror image of the other, swimming in tandem with a separation distance 2 h . A pair of robots having the swimming gait (as in Case 2) could reinforce each other’s flow and thereby increase the swimming speed as h decreases. While this would provide some insight into the boundary effects, further research is needed to fully explain the physical boundary effects. In the future the model could be extended to account for the finite dimensions of the arms and the presence of confining boundaries by using regularized Stokeslets and the method of images [26].
Our experimental system offers exciting opportunities to explore additional effects in the future. For example, the Reynolds number could be increased by adjusting the angular speed of the arms to generate inertial jets of relevance to larger crustaceans crawling along a boundary [7]. However, the results must be interpreted carefully if the air-oil interface deforms substantially. The interface must remain nearly undisturbed in order to have the immediate correspondence to a fully immersed body. Another example is to replace the rigid arms with a body equipped with flexible arms. Instead of prescribing their orientations over time, the oscillatory driving forces on them could be prescribed to better model a swimming organism. Finally, the fluid flow generated around mobile arms could be investigated. We suspect that non-swimming robots may still hover and generate intriguing flow patterns around them.

Author Contributions

Conceptualization, R.H. and D.T.; Data curation, R.H.; Formal analysis, R.H. and D.T.; Funding acquisition, D.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Science Foundation, grant number CBET-1603929.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lenz, P.H.; Takagi, D.; Hartline, D.K. Choreographed swimming of copepod nauplii. J. R. Soc. Interface 2015, 12, 20150776. [Google Scholar] [CrossRef] [Green Version]
  2. Kohlhage, K.; Yager, J. An analysis of swimming in remipede crustaceans. Phil. Trans. R. Soc. 1994, 346, 213–221. [Google Scholar]
  3. Murphy, D.W.; Webster, D.R.; Kawaguchi, S.; King, R.; Yen, J. Metachronal swimming in Antarctic krill: Gait kinematics and system design. Mar. Biol. 2011, 158, 2541–2554. [Google Scholar] [CrossRef]
  4. Zhang, C.; Guy, R.D.; Mulloney, B.; Zhang, Q.; Lewis, T.J. Neural mechanism of optimal limb coordination in crustacean swimming. Proc. Natl. Acad. Sci. USA 2014, 111, 13840. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Plotnick, R.E. Lift based mechanisms for swimming in eurypterids and portunid crabs. Trans. R. Soc. Edinb 1985, 76, 325–337. [Google Scholar] [CrossRef]
  6. Davis, W.J. Quantitative analysis of swimmeret beating in the lobster. J. Exp. Biol. 1967, 48, 643–662. [Google Scholar]
  7. Lim, J.L.; DeMont, M.E. Kinematics, hydrodynamics and force production of pleopods suggest jet-assisted walking in the American lobster (Homarus americanus). J. Exp. Biol. 2009, 212, 2731–2745. [Google Scholar] [CrossRef] [Green Version]
  8. Knight-Jones, E.W. Relations between metachronism and the direction of ciliary beat in Metazoa. Q. J. Microsc. Sci. 1954, 95, 503–521. [Google Scholar]
  9. Morgan, E. The swimming of Nymphon gracile (Pycnogonida): The swimming gait. J. Exp. Biol. 1972, 56, 421–432. [Google Scholar]
  10. Alben, S.; Spears, K.; Garth, S.; Murphy, D.; Yen, J. Coordination of multiple appendages in drag-based swimming. J. R. Soc. Interface 2010, 7, 1545–1557. [Google Scholar] [CrossRef] [Green Version]
  11. Alexander, D.E. Kinematics of swimming in two species of Idotea (Isopoda: Valvifera). J. Exp. Biol. 1988, 138, 37–49. [Google Scholar]
  12. Takagi, D. Swimming with stiff legs at low Reynolds number. Phys. Rev. E 2015, 92, 023020. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Ford, M.P.; Lai, H.K.; Samaee, M.; Santhanakrishnan, A. Hydrodynamics of metachronal paddling: Effects of varying Reynolds number and phase lag. R. Soc. Open Sci. 2019, 6, 191387. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Purcell, E.M. Life at low Reynolds number. Am. J. Phys. 1977, 45, 3. [Google Scholar] [CrossRef] [Green Version]
  15. Lighthill, J. Flagellar hydrodynamics. SIAM Rev. 1976, 18, 161–230. [Google Scholar] [CrossRef]
  16. Brumley, D.R.; Polin, M.; Pedley, T.J.; Goldstein, R.E. Metachronal waves in the flagellar beating of Volvox and their hydrodynamic origin. J. R. Soc. Interface 2015, 12, 20141358. [Google Scholar] [CrossRef] [Green Version]
  17. Hayashi, R.; Takagi, D. Asynchronous oscillations of rigid rods drive viscous fluid to swirl. Phys. Rev. Fluids 2017, 2, 124101. [Google Scholar] [CrossRef]
  18. Katz, D.F. On the propulsion of micro-organisms near solid boundaries. J. Fluid Mech. 1974, 64, 33–49. [Google Scholar] [CrossRef]
  19. Felderhof, B.U. Swimming and peristaltic pumping between two plane parallel walls. J. Phys. Condens. Matter 2009, 21, 204106. [Google Scholar] [CrossRef]
  20. Felderhof, B.U. Swimming at low Reynolds number of a cylindrical body in a circular tube. Phys. Fluids 2010, 22, 113604. [Google Scholar] [CrossRef]
  21. Liu, B.; Breuer, K.S.; Powers, T.R. Propulsion by a helical flagellum in a capillary tube. Phys. Fluids 2014, 26, 011701. [Google Scholar] [CrossRef] [Green Version]
  22. Shum, H.; Gaffney, E.A. Hydrodynamic analysis of flagellated bacteria swimming in corners of rectangular channels. Phys. Rev. E 2015, 92, 063016. [Google Scholar] [CrossRef] [PubMed]
  23. Wu, H.; Thiebaud, M.; Hu, W.F.; Farutin, A.; Rafai, S.; Lai, M.C.; Peyla, P.; Misbah, C. Amoeboid motion in confined geometry. Phys. Rev. E 2015, 92, 050701. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Liu, C.; Zhou, C.; Wang, W.; Zhang, H.P. Bimetallic Microswimmers Speed Up in Confining Channels. Phys. Rev. Lett. 2016, 117, 198001. [Google Scholar] [CrossRef] [PubMed]
  25. Demir, E.; Yesilyurt, S. Low Reynolds number swimming of helical structures in circular channels. J. Fluids Struct. 2017, 74, 234–246. [Google Scholar] [CrossRef]
  26. Ainley, J.; Durkin, S.; Embid, R.; Boindala, P.; Cortez, R. The method of images for regularized Stokeslets. J. Comp. Phys. 2008, 227, 4600–4616. [Google Scholar] [CrossRef]
Figure 1. (a) Sketch of the experimental setup. The air track is placed on top of two jacks. The robot glides on the air track and the arms of the robot are dipped in a tank of silicone oil. (b) The arms are of length L = 40 mm and separated by a distance D = 23 mm. They are dipped H = 30 mm into a tank of silicone oil. The orientation angles of Arms 1 and 2, θ 1 and θ 2 , respectively, are controlled by servos.
Figure 1. (a) Sketch of the experimental setup. The air track is placed on top of two jacks. The robot glides on the air track and the arms of the robot are dipped in a tank of silicone oil. (b) The arms are of length L = 40 mm and separated by a distance D = 23 mm. They are dipped H = 30 mm into a tank of silicone oil. The orientation angles of Arms 1 and 2, θ 1 and θ 2 , respectively, are controlled by servos.
Fluids 05 00024 g001
Figure 2. (a) The arms are at a distance h away from the floor. (b) When vertical walls were introduced, they were at a distance w from the arms.
Figure 2. (a) The arms are at a distance h away from the floor. (b) When vertical walls were introduced, they were at a distance w from the arms.
Fluids 05 00024 g002
Figure 3. The displacement of the robot when the arms move synchronously (Case 1), asynchronously with distinct median angles (Case 2), and asynchronously with same median angles (Case 3).
Figure 3. The displacement of the robot when the arms move synchronously (Case 1), asynchronously with distinct median angles (Case 2), and asynchronously with same median angles (Case 3).
Fluids 05 00024 g003
Figure 4. (a) Orientation angles of the two arms within one cycle for the three cases. (b) The mean displacement per cycle of the robot in the three experimental cases tested. The mean is obtained by taking the average over 14 cycles and the standard deviation is shown by the shaded region.
Figure 4. (a) Orientation angles of the two arms within one cycle for the three cases. (b) The mean displacement per cycle of the robot in the three experimental cases tested. The mean is obtained by taking the average over 14 cycles and the standard deviation is shown by the shaded region.
Fluids 05 00024 g004
Figure 5. Displacement of the robot in the three cases when it is far away from the floor ( h = 160 mm), near the floor ( h = 5 mm), and near the floor and wall ( h = 5 mm and w = 5 mm).
Figure 5. Displacement of the robot in the three cases when it is far away from the floor ( h = 160 mm), near the floor ( h = 5 mm), and near the floor and wall ( h = 5 mm and w = 5 mm).
Fluids 05 00024 g005
Figure 6. The net displacement per cycle at different distances h away from the floor. Markers show the net displacements per cycle, averaged over 14 cycles. Error bars show associated standard deviations. The circle, square, and diamond markers correspond to Cases 1–3, respectively. The filled markers were obtained with the arms confined by additional walls. Dashed lines show the expected net displacements per cycles according to Equation (4).
Figure 6. The net displacement per cycle at different distances h away from the floor. Markers show the net displacements per cycle, averaged over 14 cycles. Error bars show associated standard deviations. The circle, square, and diamond markers correspond to Cases 1–3, respectively. The filled markers were obtained with the arms confined by additional walls. Dashed lines show the expected net displacements per cycles according to Equation (4).
Fluids 05 00024 g006
Figure 7. An image system featuring a symmetric robot immersed completely in silicone oil. This system is obtained by reflecting the region below the air-oil interface.
Figure 7. An image system featuring a symmetric robot immersed completely in silicone oil. This system is obtained by reflecting the region below the air-oil interface.
Fluids 05 00024 g007
Figure 8. The theoretically predicted displacement of the robot compared with the experimentally measured data, obtained with the robot far away from the floor and walls.
Figure 8. The theoretically predicted displacement of the robot compared with the experimentally measured data, obtained with the robot far away from the floor and walls.
Fluids 05 00024 g008
Figure 9. Net displacement per cycle as a function of the median angles with a constant phase difference of π /2 and amplitude of 20 ° .
Figure 9. Net displacement per cycle as a function of the median angles with a constant phase difference of π /2 and amplitude of 20 ° .
Fluids 05 00024 g009
Table 1. Parameters varied in the three experimental cases: phase difference ϕ and the median orientation angles θ 1 ¯ and θ 2 ¯ of the two arms.
Table 1. Parameters varied in the three experimental cases: phase difference ϕ and the median orientation angles θ 1 ¯ and θ 2 ¯ of the two arms.
CaseDescription ϕ (rad) θ 1 ¯ (deg) θ 2 ¯ (deg)
1No phase difference09090
2Phase difference, distinct mid-angles π / 2 11070
3Phase difference, same mid-angles π / 2 9090

Share and Cite

MDPI and ACS Style

Hayashi, R.; Takagi, D. Metachronal Swimming with Rigid Arms near Boundaries. Fluids 2020, 5, 24. https://doi.org/10.3390/fluids5010024

AMA Style

Hayashi R, Takagi D. Metachronal Swimming with Rigid Arms near Boundaries. Fluids. 2020; 5(1):24. https://doi.org/10.3390/fluids5010024

Chicago/Turabian Style

Hayashi, Rintaro, and Daisuke Takagi. 2020. "Metachronal Swimming with Rigid Arms near Boundaries" Fluids 5, no. 1: 24. https://doi.org/10.3390/fluids5010024

APA Style

Hayashi, R., & Takagi, D. (2020). Metachronal Swimming with Rigid Arms near Boundaries. Fluids, 5(1), 24. https://doi.org/10.3390/fluids5010024

Article Metrics

Back to TopTop