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Flow associated with Lighthill’s elongated-body theory

Published online by Cambridge University Press:  24 April 2025

Christophe Eloy*
Affiliation:
Aix Marseille Univ, CNRS, Centrale Med, IRPHE, Marseille, France
Sébastien Michelin
Affiliation:
LadHyX, CNRS - Ecole Polytechnique, Institut Polytechnique de Paris, 91120 Palaiseau, France
*
Corresponding author: Christophe Eloy, christophe.eloy@univ-amu.fr

Abstract

The hydrodynamic forces acting on an undulating swimming fish consist of two components: a drag-based resistive force, and a reactive force originating from the necessary acceleration of an added mass of water. Lighthill’s elongated-body theory, based on potential flow, provides a framework for calculating this reactive force. By leveraging the high aspect ratio of most fish, the theory simplifies the problem into a series of independent two-dimensional slices of fluids along the fish’s body, which exchange momentum with the body and neighbouring slices. Using momentum conservation arguments, Lighthill’s theory predicts the total thrust generated by an undulating fish, based solely on the dimensions and kinematics of its caudal fin. However, the assumption of independent slices has led to the common misconception that the flow produced lacks a longitudinal component. In this paper, we revisit Lighthill’s theory, offering a modern reinterpretation using essential singularities of potential flows. We then extend it to predict the full three-dimensional flow field induced by the fish’s body motion. Our results compare favourably with numerical simulations of realistic fish geometries.

Information

Type
JFM Papers
Copyright
© The Author(s), 2025. Published by Cambridge University Press
Figure 0

Figure 1.(a) We consider a straight cylinder of length $2L$ with elliptic cross-section with semi-minor axis $a$ and semi-major axis $b$. (b) This cylinder is moving with velocity $v(t)$ along the $x$ direction. (c,d) The streamlines of the potential flow are obtained by integrating the dipoles distributed along a ribbon spanning the foci of the ellipse (represented in green).

Figure 1

Figure 2.(a) An elongated fish is swimming by undulating its backbone. The vector $\boldsymbol {s}(s,t)$ describes the planar motion of the backbone. (b,c) Illustration of the argument of momentum conservation, originally proposed by Lighthill (1971), and here adapted to a slice of fluid between $s$ and $s+\mathrm {d} s$. This slice of fluid coloured in blue has momentum per unit length $\boldsymbol{p}$, is submitted to the force $-{\boldsymbol{f}}$ by the body (red), and the pressures forces ${\boldsymbol{f}}_p$ and $-{\boldsymbol{f}}_p - \mathrm {d} {\boldsymbol{f}}_p$. In addition, a flux of momentum with velocity $-u$ goes through the slice.

Figure 2

Figure 3.Streamlines around (a,c) a swimming mackerel and (b,d) a lamprey. In (a,b), the streamlines are computed from the dipole and source densities given by (3.6) and (3.12a–c). The coloured dots in the wake show the vorticity shed given by (4.1). In (c,d), we show the numerical simulations of Borazjani & Sotiropoulos (2008, 2009) for a potential flow.

Figure 3

Figure 4.(a) Side and top views of the mackerel shape used to calculate the potential flow in figure 3(a) (Borazjani & Sotiropoulos 2008). (b) The quantities $\kappa b$, $a'$, $b'$ and $bv'/u$, assumed to be small in Lighthill’s elongated-body theory, are plotted as functions of the normalised curvilinear coordinate $s/L$. (c) Contributions to the flow field of the dipole distribution $P(s,\eta )$ in the body and in the wake. (d) Same as (c) for the contributions of the source density $Q(s,\eta )$. The background colours show levels of the flow speed, with the same scale.