First published online December 16, 2008
Journal of Experimental Biology 212, 1-10 (2009)
Published by The Company of Biologists 2009
doi: 10.1242/jeb.020404
A two-dimensional computational study on the fluid–structure interaction cause of wing pitch changes in dipteran flapping flight
Daisuke Ishihara1,*,
T. Horie1 and
Mitsunori Denda2
1 Kyushu Institute of Technology, 680-4 Kawazu, Iizuka, Fukuoka 8208502,
Japan
2 Rutgers University, 98 Brett Road, Piscataway, NJ 08854-8058, USA

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Fig. 1. Lumped torsional flexibility models. The original insect wing (A) with the
arrows indicating the region of high torsional flexibility is drawn after
Ennos (Ennos, 1988a ). The
spring model (B) shows the concept of the present lumped torsional flexibility
model, and the continuum plate model (C) shows its computational
implementation using the continuum plate. Note that the span-wise direction or
the torsional axis is perpendicular to the plane in B and C. The pitching
motion is evaluated using the angular displacement or pitch angle a,
which is the slope angle of the trailing edge of the wing as shown in C.
U(t), x-displacement of the wing base.
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Fig. 2. Wing torsion during the downstrokes (A) and upstrokes (B) drawn after Ennos
(Ennos, 1988a ). Most of the
wing torsional flexibility in Diptera is concentrated on the narrow basal and
short root regions of the wings, and allows the wing to twist around its
torsional axis in a span-wise direction.
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Fig. 3. A single degree of freedom mass–spring–dashpot system of the
wing. U(t) and u(t),
x-displacement of the wing base and center, respectively;
mw, wing mass; ks, spring constant;
F, force; c, chord length; M, moment.
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Fig. 4. The relationship between the frequency ratio
f/fn and the phase shift b for the
damping ratios =0.5 (red line), 1 (blue line) and 2 (black line).
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Fig. 5. (A) Schematic view of the analysis domain, and (B) the finite element mesh.
A unit length in the z-direction is assumed.
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Fig. 6. Time histories of the lift (CL, A) and drag
(CD, B) coefficients for the wing motion of the flexible
wing with the passive pitching (black line) and the wing motion of the rigid
wing using this passive pitching as the active one (red line).
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Fig. 7. Time histories of the simulated passive pitching motion (A) and the
normalized lift coefficient CL generated by it (B). The
pitching motion is evaluated using the angular displacement or pitch angle
a, which is the slope angle of the trailing edge of the wing. The
vertical lines and the attached arrows show the range of each half-stroke for
the downstroke (Down) and upstroke (Up).
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Fig. 8. The frame-by-frame advance of the wing motion from 7 to 8 cycles. The time
interval between each frame is 0.01 cycles. The wing chord moves from right to
left in the downstroke 7 to 7.5 cycles (A) and left to right in the upstroke
7.5 to 8 cycles (B). The arrows indicate the flapping direction.
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Fig. 9. Fluid velocity fields from 7 to 7.9 time cycles for the crane fly (Reynolds
number Re=290, Strouhal number St=0.054, corresponding to
A0/c=5.9, where A0 is stroke
amplitude). The time interval between each snapshot is 0.1 cycles. The arrows
point in the direction of fluid velocity with their color indicating the
magnitude; pink and blue correspond to Vmax=35 cm
s–1 and 0, respectively. The wing chord is represented by the
white line. Columns A and B represent the downstroke (from 7 to 7.4 cycles)
and the upstroke (from 7.5 to 7.9 cycles), respectively. The wing moves from
right to left during the downstroke and from left to right during the
upstroke. The white arrows indicate the positions of the leading edge
vortices. The figures in the left column show that the leading edge vortex was
detached from the wing at the middle of the downstroke and then reproduced.
The figures in the right column show that the leading edge vortex was loosely
attached to the wing.
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Fig. 10. Fluid velocity fields from 4 to 4.9 time cycles for the fictitious insect
(Re=200, St=0.1 corresponding to
A0/c=3.2). The time interval between each
snapshot is 0.1 cycles. The arrows point in the direction of the fluid
velocity with their color indicating the magnitude; pink and blue correspond
to Vmax=24 cm s–1 and 0, respectively.
The wing chord is represented by the white line. Columns A and B represent the
downstroke (from 4 to 4.4 cycles) and the upstroke (from 4.5 to 4.9 cycles),
respectively. The wing moves from right to left during the downstroke and from
left to right during the upstroke.
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Fig. 11. Time histories of the lift coefficient CL for the
fictitious insect (red line) and the crane fly (black line). Note that both
traces show simulations (not experimental data), and that in the fictitious
insect case the leading edge vortex does not separate because of the short
length of translation. The vertical lines and the attached arrows show the
range of each half-stroke for the downstroke (Down) and upstroke (Up).
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Fig. A1. The two-dimensional wing model similar to that used by Wang and colleagues
(Wang et al., 2004 ) as a
benchmark to test the capability of our method. The x-displacement
U(t) and an angular displacement around the
z-direction a(t) are actively applied to the wing
center.
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Fig. A3. Time histories of CL and CD for the
different positions of the axis of rotation. The black, red, blue and green
lines correspond to positions O (centre), A (top), B (upper 1/10) and C (upper
1/3), respectively.
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Fig. A4. The relationship between the rotational axis positions and the second peak
values of the force coefficients from 3.5 to 4 cycles in
Fig. A3.
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Fig. A5. Convergence test where the fluid grid is refined. Mesh O (the number of
nodes and elements is 3417 and 6600, respectively) is used to give the results
in Figs A2,
A3 and
A4. The refined meshes A (the
number of nodes and elements is 3905 and 7560, respectively) and B (the number
of nodes and elements is 4697 and 9120, respectively) have 1.4 and 2 times
finer space resolutions, respectively, around the wing.
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Fig. A6. Comparison of the time histories of CL and
CD. The black, blue and red lines show the results
obtained using meshes O, A and B, respectively.
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© The Company of Biologists Ltd 2009