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Filament mechanics in a half-space via regularised Stokeslet segments

Published online by Cambridge University Press:  01 October 2019

B. J. Walker*
Affiliation:
Wolfson Centre for Mathematical Biology, Mathematical Institute, University of Oxford, Oxford OX2 6GG, UK
K. Ishimoto
Affiliation:
Graduate School of Mathematical Sciences, The University of Tokyo, Tokyo, 153-8914, Japan
H. Gadêlha
Affiliation:
Department of Engineering Mathematics, University of Bristol, Bristol BS8 1UB, UK
E. A. Gaffney
Affiliation:
Wolfson Centre for Mathematical Biology, Mathematical Institute, University of Oxford, Oxford OX2 6GG, UK
*
†Email address for correspondence: benjamin.walker@maths.ox.ac.uk

Abstract

We present a generalisation of efficient numerical frameworks for modelling fluid–filament interactions via the discretisation of a recently developed, non-local integral equation formulation to incorporate regularised Stokeslets with half-space boundary conditions, as motivated by the importance of confining geometries in many applications. We proceed to utilise this framework to examine the drag on slender inextensible filaments moving near a boundary, firstly with a relatively simple example, evaluating the accuracy of resistive force theories near boundaries using regularised Stokeslet segments. This highlights that resistive force theories do not accurately quantify filament dynamics in a range of circumstances, even with analytical corrections for the boundary. However, there is the notable and important exception of movement in a plane parallel to the boundary, where accuracy is maintained. In particular, this justifies the judicious use of resistive force theories in examining the mechanics of filaments and monoflagellate microswimmers with planar flagellar patterns moving parallel to boundaries. We proceed to apply the numerical framework developed here to consider how filament elastohydrodynamics can impact drag near a boundary, analysing in detail the complex responses of a passive cantilevered filament to an oscillatory flow. In particular, we document the emergence of an asymmetric periodic beating in passive filaments in particular parameter regimes, which are remarkably similar to the power and reverse strokes exhibited by motile $9+2$ cilia. Furthermore, these changes in the morphology of the filament beating, arising from the fluid–structure interactions, also induce a significant increase in the hydrodynamic drag of the filament.

Information

Type
JFM Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s) 2019
Figure 0

Figure 1. The two-dimensional piecewise-linear filament. We consider an inextensible filament composed of $N$ straight segments each of length $v_{i}$, connected at material points $\boldsymbol{x}_{i}$ with each segment making angle $\unicode[STIX]{x1D703}_{i}$ with the global $\boldsymbol{e}_{x}$ axis. The endpoints $\boldsymbol{x}_{1}$ and $\boldsymbol{x}_{N+1}$ shall be referred to as the base and tip respectively, and we note that, given segment lengths $v_{i}$, the entire filament may be described by the location of the base and the angles $\unicode[STIX]{x1D703}_{i}$.

Figure 1

Figure 2. Schematic configurations of planar filaments near boundaries. (a) A filament moving parallel to the infinite planar boundary, at constant separation $h$. The projection of the filament onto the boundary is shown as a thin black line. (b) A filament contained in a plane perpendicular to the boundary, with the plane of motion shown dashed.

Figure 2

Figure 3. Computed total drag on a straight parallel filament moving along a boundary parallel to its tangent, here with $\unicode[STIX]{x1D716}/L=10^{-2}$. (a) Near the boundary we see very good agreement between the regularised Stokeslet segment (RSS) solution (dot-dashed) and the wall-corrected resistive force theory (W-RFT) solution of Katz et al. (solid), with the latter corresponding to (2.33) and fair agreement maintained outside the region of validity of W-RFT as $h/L\sim 1$. The boundary element method (BEM) data of Ramia et al. are marked with squares, adapted from Ramia et al. (1993, figure 4c) and show good agreement with the regularised Stokeslet segments. (b) Similar agreement can be seen far from the boundary, with the asymptotic solution of Brenner given in (2.32) losing validity when $h/L\sim 1$ although remaining within 10 % of the RSS solution.

Figure 3

Figure 4. Drag calculations from kinematic data captured parallel to a planar boundary, with data from Ishimoto et al. (2017). (a) The tangential and normal components of the drag along the filament for a single frame (upper and lower panels respectively) at separation $h/L=0.01$, showing good qualitative agreement between methodologies of drag computation and fair quantitative agreement between W-RFT and RSS. (b) The magnitude and direction of the total integrated force on the filament (upper and lower panels respectively) at separation $h/L=0.01$, with direction measured relative to an arbitrary fixed axis. As in (a), agreement is fair and qualitative features are captured by all methodologies. Remarkably, the direction of the resultant force as computed using the resistive force theories strongly agrees with that of the non-local RSS. Endpoint effects are visible in the upper panel of (a), as discussed in detail in § 2.5. (c) Ratio of effective drag coefficients $C_{n}/C_{t}$, as computed via RSS, against boundary separation (upper), shown as the median over all frames and all material points (740 frames, 100 points per frame). The ratio as predicted by Katz et al., 2, is shown as a dashed line for comparison. Error bars corresponding to half the interquartile range are shown, representative of dispersal about the median as the distributions do not appear significantly skewed. Modifying the kinematic data of Ishimoto et al. (2017) as described in the main text to simulate a pinned filament, analogous results are shown in red (dotted, thin), highlighting a reduction in validity of resistive force theories for pinned data but retaining notable accuracy when very close to the boundary. The lower panel is a histogram corresponding to $h/L=0.01$, showing the distribution of effective coefficient ratios in the free-swimming case, highlighting tight grouping about the median. (d) Median values of effective resistive coefficients against boundary separation (upper), with error bars of half the interquartile range. Pinned data are shown in red (dotted, thin) for comparison. The lower panel is a histogram corresponding to $h/L=0.01$, showing the tight distribution of dimensionless effective drag coefficients $C_{n}/\unicode[STIX]{x1D707}$ and $C_{t}/\unicode[STIX]{x1D707}$, with $C_{t}/\unicode[STIX]{x1D707}$ shown darker. Medians are shown dashed.

Figure 4

Figure 5. Drag computation for pinned spermatozoa with a base clamped perpendicular to a boundary over a single period of 100 frames. (a) Normalised total force on the boundary over a single beat period as computed by regularised Stokeslet segments (dot-dashed) and free-space resistive force theory (dotted), in the cases of hyperactive and normal beating patterns (high and low amplitudes respectively). Normal beating gives rise to a force on the boundary of unchanging sign, whilst hyperactivated beating generates a force whose sign changes over the beat period, corresponding to a so-called tugging effect. (b) Tangential (upper panel) and normal components (lower panel) of force density as a function of arclength for a single frame, shown for the hyperactivated beat pattern. In contrast to the fair agreement between methods seen in (a), with mean error of 24 % for the hyperactivated beat between F-RFT and RSS, tangential force density differs on average by 43 % between methods for the frame shown. (c) Ratio between effective drag coefficients computed using regularised Stokeslet segments, with contours of zero filament curvature superimposed as black curves, showing significant variation in the effective ratio.

Figure 5

Figure 6. Periodic beating of a cantilevered filament in oscillatory background flow of amplitude $\hat{a}=2\unicode[STIX]{x03C0}$, shown here over a single period of the background flow after convergence to periodic filament motion has occurred. (a) At low sperm numbers, here with $Sp=1.14$, flow-driven beating is approximately symmetric. (b) For medium sperm numbers a remarkable ciliary-type asymmetric beating emerges, shown here for $Sp=2.84$ and globally stable, with a clear distinction between effective forward and reverse strokes. (c) At higher sperm numbers the filament buckles significantly and regains a symmetric periodic beat, here with $Sp=4.55$. (d–f) Plots of signed curvature corresponding to (a–c) above, sampled at 100 frames per period and each independently scaled for clarity, with select contours of curvature shown. Symmetry is clearly visible in (d) and (f), with the latter displaying a low-order buckling mode. (e) Exemplifies cilia-like beating, with the effective power stroke occurring approximately between frames 20 and 60 (shown black, dashed).

Figure 6

Figure 7. Bifurcation into high-order buckling modes for a filament with high sperm number, here with $Sp=16$ and sampled at 100 frames over the initial period of the background flow. (a) A single frame of the initial motion of the filament, where high-curvature regions can be seen to be resolved by the $N=150$ segments used here, with curvature represented by colour. (b) The curvature of the filament over the latter part of the initial period of the background flow, from which we may identify the collapse of high-order modes onto lower-order buckling modes. The frame shown in (a) is indicated on the curvature plot by a dashed line, with colour scalings consistent between plots. (c) A bifurcation diagram highlighting the regions of parameter space corresponding to low-amplitude symmetric, ciliary and buckled modes of beating. Buckled modes appear to the right of the dividing dashed line, as defined by the transition between less than three and three regions of constant curvature sign along the filament. Furthermore, ciliary beating occurs within contours delimiting where $S$ is essentially unity, shown shaded. In the overlap region between ciliary and buckled beating we observe ciliary-type beats with buckled tips.

Figure 7

Figure 8. Hydrodynamic drag associated with cantilevered filaments in oscillating flow over a single period. (a) Total drag on the filament in the direction parallel to the boundary, averaged over a single period. A steep increase in total drag is noted to occur upon entering the parameter regime of ciliary beating, with a less-prominent local maximum present around $Sp=1$. (b) Total pushing force applied on the base of the filament in the direction perpendicular to the boundary over a single period of the background flow. A clear maximum can be seen around $Sp=1$, corresponding to the symmetric beating of stiff filaments, with the high sperm number border of the ciliary region being aligned with a sharp, albeit limited increase in total drag for $\hat{a}>6$. (c) Maximum instantaneous total drag on the filament in the direction parallel to the boundary. Comparison with (a) highlights gross total drag cancellation occurring for low $Sp$, with reduced cancellation for the asymmetric ciliary-type beating. (d) Maximum absolute instantaneous force applied on the base of the filament in the direction perpendicular to the boundary. By comparison with (b) we observe limited cancellation of total drag in this direction in stiff filaments, with significant cancellation occurring for ciliary-type beating. Each panel is normalised by the maximum instantaneous total parallel drag and rescaled by flow amplitude to enable meaningful comparison. Select contours of total drag are shown and the region of ciliary-type beating is outlined in black, the latter determined only from the kinematic symmetry measure $S$.

Figure 8

Figure 9. Evaluating the sensitivity of long-time behaviour to background flow phase. (a) An illustration of the measure $\hat{x}_{max}$ used to determine periodicity and convergence of filament behaviour, equal to the maximal displacement of the filament tip from the centreline over one period of the background flow. Filament configurations throughout one period of motion are shown as coloured curves. (b) The evolution of $\hat{x}_{max}$ over 40 periods of the background flow, for various choices of initial phase $\hat{t}_{0}\in [0,\unicode[STIX]{x03C0}]$, here for $Sp=3.13$, $\hat{a}=2\unicode[STIX]{x03C0}$. In the upper panel we see that all choices of $\hat{t}_{0}$ lead to convergence to the same behaviour, with even the approximate initial symmetry of the $\hat{t}_{0}=\unicode[STIX]{x03C0}/2$ instance (dashed) collapsing onto the common limiting behaviour. A posteriori validation of convergence to periodic motion from all phases is provided by consideration of the per cycle change in $\hat{x}_{max}$, as shown in the lower panel and highlighting eventual periodicity. Symmetric counterparts for $\hat{t}_{0}\in [\unicode[STIX]{x03C0},2\unicode[STIX]{x03C0}]$ have been omitted. (c) Signed curvature of the filament during the first periods of the background flow, with select contours of curvature shown, and sampled at 100 frames per period for $\hat{t}_{0}=3\unicode[STIX]{x03C0}/8$, showing the transition to ciliary beating from a straight initial configuration.

Figure 9

Figure 10. The limiting deflections of cantilevered filaments in background shear flows, with elastohydrodynamic numbers $E_{h}\approx 34,68,85$ (black, solid), compared with data adapted from Pozrikidis (2010, figure 11) and corresponding to $\hat{E}_{B}=1.0,0.5,0.4$ from the publication of Pozrikidis. The latter data are shown as red circles, with good agreement between solutions, serving as validation of our treatment and implementation of the governing elastohydrodynamics. Here $N=80$ and $\unicode[STIX]{x1D716}/L=0.05$, the latter in line with the set-up of Pozrikidis (2010).

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