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First published online August 30, 2006
Journal of Experimental Biology 209, 3558-3568 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02469
Effective elastic modulus of isolated gecko setal arrays

1 Department of Biology, Lewis & Clark College, Portland, OR 97219,
USA
2 Department of Electrical Engineering and Computer Science, University of
California, Berkeley, CA 94720, USA
* Author for correspondence (e-mail: autumn{at}lclark.edu)
Accepted 5 June 2006
| Summary |
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Key words: gecko, adhesion, pressure sensitive adhesive, material science, contact mechanics, biomechanics
| Introduction |
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Cantilever model
Current studies of setal deformation generally treat a single seta as a
cylindrical elastic rod of radius R with a modulus of elasticity
E and area moment of inertia I=
R4/4.
When a load F is applied to the tip of the rod in the direction
perpendicular to the supporting substrate, the rod will deform and the tip
will displace by an amount
in the same direction.
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is
only significant after a critical buckling load is exceeded. For this special
case, the seta is represented by a column buckling model
(Jagota and Bennison, 2002
denote the natural
(undeformed) slope of the seta with respect to the surface of the supporting
substrate. When
is less than 90°, a more general theory is used to
study setal deformation. The elastica model
(Frisch-Fay, 1962
as a
function of load F:
![]() | (1) |
where F(,) and E(,) are the
elliptic integrals of the first and second kind, respectively,
n=
/2, k=(F/EI)1/2,
m=arcsin(sin(
/4-
/2)/p), and the modulus p
is the solution to:
![]() | (2) |
The modulus p is determined numerically over the domain
sin(
/4-
/2) to sin(3
/4-
/2) by solving Eqn 2 with a
nonlinear equation solver in Matlab 7 (The Mathworks Inc., Natick, MA, USA).
Substituting the solution for p into Eqn 1 yields a relationship
between the applied load F and the resulting tip displacement
. Plots of F vs
for values of
ranging from 30
to 90° are given in Fig.
3A.
Following arguments (Frisch-Fay,
1962
), Eqn 1 can be modified to admit an additional shear load
V that acts on the tip in the direction parallel to the surface of
the supporting substrate. This force is generated when the setal array is
dragged along the surface during compressive loading. The magnitude is limited
by Coulomb friction (Bhushan,
2002
) and so in general:
![]() | (3) |
where the friction coefficient µ is typically 0.25 for polymeric surfaces, and where S is the shear strength due to interfacial adhesion. Since measurements are performed on a TeflonTM substrate with relatively large compressive loads, the contribution of adhesion to the shear force is negligible and so Eqn 3 is assumed to reduce to |V|=µF.
Interestingly, for a rod with a natural deflection of 45°
(
<
/4), elastic rod theory predicts that under a combined loading
F and V=µF, the rod becomes more compliant for
low F. If, however, the rod is dragged against its natural
orientation (i.e. V=-µF), it becomes stiffer. This can be
seen more simply by examining the linearized approximation to elastica.
For a naturally angled seta, Eqn 1 may be simplified by assuming that
deformation is governed by small-deflection cantilever bending. In this
cantilever bending approximation, loads parallel to the beam cause no
deflection and loads transverse to the beam cause a transverse deflection
governed by spring constant 3EI/L3. Finding the
transverse components of F and V=±µF, and
computing the normal component of the resulting deflection yields the
following relationship between tip forces and the normal displacement
(Campolo et al., 2003
;
Sitti and Fearing, 2003
),
![]() | (4) |
As illustrated in Fig. 3B, this simple model predicts the same trend as elastica: higher stiffness when V=-µF (sliding against the hair), intermediate stiffness when V=0 (no sliding), and lower stiffness when V=µF (sliding with the hair).
Next, to derive an effective elastic modulus (Eeff) for
a model setal array, we use Hooke's law,
![]() | (5) |
where
is the stress applied to the setal array and
is the
resulting strain, both along the perpendicular axis. For a setal density
D, which has units of inverse area, the stress may be represented as,
![]() | (6) |
The resulting strain is defined as
=
/(Lsin
).
Substituting
approx for
yields:
![]() | (7) |
Lastly, substituting the expressions for
and
given in Eqn 6
and Eqn 7 into Eqn 5 and solving for Eeff gives:
![]() | (8) |
We now calculate the shaft angle
required to yield an effective
stiffness of 100 kPa (the upper limit of Dahlquist's criterion)
(Dahlquist, 1969
;
Pocius, 2002
). A typical tokay
setal array has approx. 14 000 setae mm-2
(Schleich and Kästle,
1986
) and D=1.44x1010 m-2.
Using Eqn 3, a value of
=50° is required for E=1 GPa, and
=36.65° for E=2 GPa to yield Eeff=100
kPa.
A template is the simplest model (fewest number of variables and
parameters) that exhibits a targeted behavior
(Full and Koditschek, 1999
).
This study focuses on evaluating the validity of the cantilever model as a
template for setal deformation. We measured the forces associated with
deformation of gecko setal arrays to test the hypotheses that (1) forces of
deformation are an approximately linear function over the working range of
displacements, as predicted by the cantilever model; (2)
Eeff is below 100 kPa, as predicted by the Dahlquist
criterion, and (3) stiffness is greater when the angle of deformation is
negative (against the natural path of drag) than during vertical or positive
angle deformations.
| Materials and methods |
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Mechanical testing apparatus
Setal array specimens were mounted on SEM stubs and evaluated with a custom
2-axis mechanical tester (Fig.
4). The specimen chuck was attached to a Kistler 9328A 3-axis
force sensor (Kistler, Winterthur, Switzerland) that was moved in the
Z (up-and-down) and Y (left-and-right) axes with Newport
460P stages (Newport, Irvine, CA, USA) driven by closed loop brushless DC
servomotors (Newport 850G-HS actuator in the Y axis and a Newport
850G actuator in the Z axis). The stage and force sensor assembly
were vertically mounted to a stainless steel `tombstone' above a Newport RP
Reliance breadboard table. A Newport ESP 300 servocontroller drove the
actuators. Force measurements were collected through an AD Instruments
Maclab/4e data acquisition unit (ADInstruments, Milford, MA, USA). The stage
controller and force acquisition were interfaced with a Powerbook G3 (Apple
Computer, Cupertino, CA, USA) for automated control of array experiments. The
stiffness of the 2-axis mechanical tester was measured by pressing a blank SEM
stub into the breadboard table. The stiffness of the mechanical tester itself
was about 320 N mm-1. Pilot experiments showed that the setal
arrays stiffness was in the range of 0.5-3 N mm-1. Therefore, the
primary compliant element in the test arrangement was the setal array itself.
Test substrates are held in place by toggle strap clamps with spring plungers
bolted to the Newport breadboard table. Array test specimens were mounted in
the mechanical tester chuck so that their natural path of drag was in
alignment with the Y axis. The array alignment was carried out with
the help of a mirror. The compliant nature of the setal arrays allowed for
small rotational misalignments without impacting the measurement of array
physical properties.
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Setal array dimension
Estimation of the setal array modulus requires measurement of the array
dimensions. After mounting arrays to SEM stubs, the specimens were inspected
using a SMZ 1500 optical stereomicroscope (Nikon, Yokohama, Kanagawa, Japan)
to ensure that the arrays were securely glued and the setae were free of glue
that would interfere with the physical property measurements. Defective arrays
were rejected from the study. Array area was measured by photographing each
array under the optical microscope with 100 µm diameter stainless steel
`minutien' pins (Fine Science Tools, product number 26002-10, North Vancouver,
BC, Canada) as a size reference. The digitized micrographs were examined with
Canvas v. 9 (ACD, Saanichton, BC, Canada) drawing software to measure the area
of each array.
After mechanical testing of the arrays, the stub-mounted specimens were prepared for SEM observation. Array specimens were platinum-palladium sputter-coated using a Hummer VI plasma coater (Technics, Anatech Ltd, Denver, NC, USA). Each of the test specimens was then viewed in an Amray 1810 SEM (Amray, KLA-Tencor, Milpitas, CA, USA). Five photomicrographs were taken along the length of each array. The digitized photomicrographs were imported into Canvas 9 software for assessment of array height.
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![]() | (9) |
The setal stiffness normalizes the data by array area. We then estimated
the effective Young's modulus of a setal array, Eeff, by
measuring the array height, L0, and assuming the applied
compression load is distributed evenly over the measured array area (i.e. a
lower estimate of modulus). We used linear regression to evaluate the
significance of linearity of the force-displacement curves, after trimming the
period during initial preload. The statistically linear portion of the array
tap data were modeled with Hookean elasticity where compression stress,
, is a linear function of strain,
, giving modulus as:
![]() | (10) |
Now, the modulus can be expanded to:
![]() | (11) |
where F is the applied load and
L is the change in
array height in response to this force. If the setal array behaves as a
Hookean spring and substituting
![]() | (12) |
into Eqn 11 gives the following expression for the effective modulus:
![]() | (13) |
Setal array coefficient of friction The coefficient of friction,
µ, for the `along drag' and `against drag' conditions can be assessed since
there is a sliding phase across the PTFE test substrate. The coefficient of
friction is calculated as:
![]() | (14) |
| Results |
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Effect of age of specimen
The age of the primary group of specimens (time after harvest) ranged from
2 h to 28 days. Over this time period, there was a subtle yet statistically
significant (P<0.001) increase in stiffness over time after
harvest. Linear regression revealed that arrays increased in stiffness by an
average of 2.08 kPa per day. The effect of age on stiffness did not differ
significantly among loading treatments. We also tested five setal arrays
ranging in age from 881 to 894 days (approx. 2.4 years).
Eeff averaged 30.7 kPa lower in aged arrays, yet the
effect of loading direction on Eeff was similar to that on
fresh arrays. In aged arrays, Eeff during vertical and
+45° compression were 62±2.4 kPa and 53±2.1 kPa (mean
± s.e.m.), respectively. Eeff during -45°
compression was 73±3.2 kPa. Mean coefficient of friction (µ) in aged
arrays during the drag step was similar to that of fresh arrays; µ was
0.26±0.016 in the -45° trials, 0.24±0.016 in the +45°
trials, and did not differ statistically between +45 and -45 loading
directions (t=0.852; d.f.=97; P=0.39).
| Discussion |
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The structural complexity of the setae, and their arrangement in arrays
(Figs 1,
2), suggest that complex models
may be needed to predict system function fully. It is advisable, however, to
begin with a template model (Full and
Koditschek, 1999
), the simplest model (fewest number of variables
and parameters) that best describes system behavior. Templates may then be
grounded in more detailed (anchored) models to ask specific questions. This
study suggests that the cantilever model is a good template for the behavior
of setal arrays under loading and unloading conditions.
Support for the cantilever model
Highly linear forces of deformation under all loading directions support
the validity of the cantilever model, and of identifying a single value of the
effective modulus of the array. Eeff of setal arrays
during vertical and +45° compression (along the natural path of drag and
curvature of the setae)
The measured compliance under all loading directions supports the validity of the cantilever model. This correlation, however, appears strongest at larger displacements. As evident in Figs 6 and 7, arrays were significantly more compliant at the start of loading. We believe that this initial compliance is due to height variation in the setae, which prevent some of the setae from making initial contact and contributing to the deformation resistance. At larger displacements, complete contact is expected, leading to an effective stiffening of the array. As shown in Fig. 7, both contact regimes exhibit a linear force-displacement relationship. After initial contact, Eeff of setal arrays during vertical and +45° compression increased to 83±4.0 kPa and 86±4.4 kPa (mean ± s.e.m.), respectively. As predicted, the measured compliance satisfied Dahlquist's condition for tack (Eeff<100 kPa). Setae became significantly stiffer when compressed against the natural path of drag: Eeff during -45° compression was 110±4.7 kPa. Using Eqn 8, we arrive at a predicted value of 67.8 kPa for +45° compression, 20% below the observed value of 86 kPa. Eqn 8 yields a highly accurate predicted value of 113.8 kPa for -45° compression.
Additionally, we observed values of the resting angle of setal shafts
(
) for tokay gecko setae near 43°, consistent with the cantilever
model. The difference in stiffness between fresh and aged setal arrays
provided an opportunity to test the generality of the anisotropic stiffness
effects we observed. Aged arrays were softer by approx. 30%, yet the forces of
deformation followed a similar pattern as for fresh arrays, in which -45°
compression resulted in significantly increased stiffness. The mechanism
underlying the change in stiffness over time remains unknown, and merits
further investigation. However, only changes over the timescale of the shed
cycle of the animal (approximately 2 months) will be biologically
relevant.
It is interesting to note that using the full expression in Eqn 3 for shear
leads to a prediction of an effective friction coefficient that is compatible
with experimental measurements. The effective friction coefficient
µeff is defined as the ratio of the measured shear force to the
applied compressive load. Mathematically, this may be represented as
![]() | (15) |
Since the setal array is more compliant under +45° compression, a smaller load F is necessary to achieve a prescribed normal displacement. Hence, by Eqn 15, the effective friction coefficient is expected to be larger for +45° than for -45° compression. This is consistent with the values of µ of 0.24 and 0.29 measured for the -45° and +45° trials, respectively.
We conclude that, unlike synthetic PSAs, setal arrays can be modeled as Hookean elastic solids. A good template model for a setal array is a bed of springs with a directional stiffness. A linear spring rate will assist in alignment of the adhesive spatular tips with the contact surface over a wide range of displacement.
Requirements for attachment
Previously, we measured the adhesive and shear force of a single isolated
gecko seta on an aluminum wire (Autumn et
al., 2000
). A small normal preload force, combined with a 5 µm
shear displacement (proximally, along the natural path of the seta) yielded a
very large shear force of 200 µN, 32x the force predicted by
whole-animal measurements (Irschick et
al., 1996
) and 100x the frictional force measured with the
seta oriented with spatulae facing away from the surface
(Autumn et al., 2000
). Preload
and drag steps were necessary to initiate significant adhesion in isolated
gecko setae, likely because mechanical deformation is needed to achieve a high
contact fraction with the substrate. Autumn and Hansen estimated that only
6.6% of the area at the tip of a seta is available for initial contact with a
surface when setae are in their unloaded state
(Autumn and Hansen, 2006
). This
suggests that initially, during a gecko's foot placement, the contact fraction
of the distal region of the setal array must be very low. Yet the dynamics of
the foot must be sufficient to increase the contact fraction substantially to
achieve the extraordinary values of adhesion and friction that have been
measured in whole animals (Autumn et al.,
2002
; Hansen and Autumn,
2005
; Irschick et al.,
1996
) and isolated setae
(Autumn et al., 2000
;
Autumn et al., 2002
;
Hansen and Autumn, 2005
). To
achieve attachment the contact fraction must increase from 6% to 46%, or by
approx. 7.5-fold, following preload and drag.
With the results of this study, we can now estimate the magnitude of force
and deformation required to cause this increase in contact fraction. In
isolated gecko setae, a 2.5 µN preload was sufficient to yield peak
adhesion of between 20 µN (Autumn et
al., 2000
) and 40 µN (Autumn
et al., 2002
). (For contact with aluminum
(Autumn et al., 2000
) or
silicon (Autumn et al., 2002
),
the shear term S in Eqn 3 will dominate, whereas we assume S
to be negligible for contact with TeflonTM in this study.] A normal
displacement of 31.1 µm is required to yield 2.5 µN of preload force,
given the stiffness value measured in this study
(kseta=0.0804 N m-1;
Table 1). The value of 31.1
µm represents about half the compressive range of a typical setal array in
our study.
|
Requirements for detachment
The surprisingly large forces generated by single setae raised the question
of how geckos manage to detach their feet in just 15 ms with no measurable
detachment forces (Autumn et al.,
2006
). Increasing the angle that the setal shaft makes with the
substrate to 30° causes detachment
(Autumn et al., 2000
). Our
estimates of the setal angle in arrays in their unloaded default state was
43° in this study, suggesting that elastic energy may be stored as the
setae are bent during preload, drag and adhesion. Furthermore, a resting shaft
angle of 43° suggests that setae could release spontaneously if loading is
relaxed sufficiently.
Effect of cantilever model parameters on system performance
The cantilever model suggests that thinner setal shafts should decrease
Eeff and promote a greater contact fraction on rough
surfaces (Campolo et al.,
2003
; Jagota and Bennison,
2002
; Meine et al.,
2004
; Persson,
2003
; Persson et al.,
2005
; Persson and Gorb,
2003
; Scherge and Gorb,
2001
; Sitti and Fearing,
2003
; Spolenak et al.,
2005
; Stork,
1983
). The cantilever model also suggests that longer and softer
setal shafts, and a lower shaft angle
will result in better adhesion on
rough surfaces because these parameters will reduce Eeff.
On a randomly rough surface, some setal shafts should be bent in compression
(concave), while others will be bent in tension (convex). The total force
required to pull off a setal array from a rough surface should therefore be
determined by the cumulative adhesive force of all the attached spatulae,
minus the sum of the forces due to elastic deformation of compressed setal
shafts. Our results suggest that aged setal arrays have a lower
Eeff, and should therefore be able to conform to rough
surfaces better than stiffer, fresh arrays.
If setae mat together (Stork,
1983
), it is likely that adhesive function will be compromised.
Interestingly, the same parameters that promote strong adhesion on rough
surfaces should also cause matting of adjacent setae
(Glassmaker et al., 2004
;
Hui et al., 2004
;
Persson, 2003
;
Sitti and Fearing, 2003
;
Spolenak et al., 2005
). The
distance between setae and the stiffness of the shafts will determine the
amount of force required to bring the tips together for matting to occur. It
follows from the cantilever model that stiffer, shorter and thicker stalks
will allow a greater packing density without matting. Spolenak et al. devised
`design maps' for setal adhesive structures
(Spolenak et al., 2005
), an
approach for visualizing the parametric trade-offs needed to satisfy the rough
surface and antimatting conditions while at the same time maintaining
structural integrity of the material. Spolenak et al. used an estimate of
Eeff=1 MPa for their predictions
(Spolenak et al., 2005
). The
results of this study indicate that this value is an order of magnitude too
high - at least for tokay gecko setae, which have a value of
Eeff of approximately 100 kPa. Comparative study of setae
in other geckos will be an important area of future work. It remains unknown
if Eeff is similar in other species of gecko, Anolis,
Prasinohaema and seta-bearing arthropods.
Smart adhesion at the limit of tack
There is emerging evidence that an array of gecko setae can act like a
tacky, deformable material, while individual setae and spatulae retain the
structural integrity of stiff protein fibers. This may enable the gecko
adhesive to tolerate heavy, repeated use without creep or degradation. Indeed
theoretical considerations suggest that the fibrillar structure of the gecko
adhesive can be thought of as a permanent craze
(Jagota and Bennison, 2002
;
Persson, 2003
) that can raise
the fracture energy relative to a solid layer of adhesive material. As with
polymer crazes, setal structures under stress could store energy elastically
in each seta of the array, and then as setae are pulled off, elastic energy
could be dissipated internally without contributing to propagation of the
crack between the adhesive and substrate
(Hui et al., 2004
;
Jagota and Bennison, 2002
;
Persson, 2003
). Unlike polymer
crazes, setal structures may dissipate energy primarily elastically rather
than plastically.




| Acknowledgments |
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| Footnotes |
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Present address: Dept of Electrical and Computer Engineering, Clemson
University, Clemson, SC 29634, USA | References |
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Alibardi, L. (2003). Ultrastructural autoradiographic and immunocytochemical analysis of setae formation and keratinization in the digital pads of the gecko Hemidactylus turcicus (Gekkonidae, Reptilia). Tissue Cell 35,288 -296.[CrossRef][Medline]
Autumn, K. (2006). Properties, principles, and parameters of the gecko adhesive system. In Biological Adhesives (ed. A. Smith and J. Callow), pp.225 -255. Berlin, Heidelberg: Springer-Verlag.
Autumn, K. and Hansen, W. (2006). Ultrahydrophobicity indicates a nonadhesive default state in gecko setae. J. Comp. Physiol. A Sens. Neural Behav. Physiol. doi:10.1007/s00359-006-0149-y .
Autumn, K. and Peattie, A. (2002). Mechanisms
of adhesion in geckos. Integr. Comp. Biol.
42,1081
-1090.
Autumn, K., Liang, Y. A., Hsieh, S. T., Zesch, W., Chan, W.-P., Kenny, W. T., Fearing, R. and Full, R. J. (2000). Adhesive force of a single gecko foot-hair. Nature 405,681 -685.[CrossRef][Medline]
Autumn, K., Sitti, M., Peattie, A., Hansen, W., Sponberg, S.,
Liang, Y. A., Kenny, T., Fearing, R., Israelachvili, J. and Full, R. J.
(2002). Evidence for van der Waals adhesion in gecko setae.
Proc. Natl. Acad. Sci. USA
99,12252
-12256.
Autumn, K., Hsieh, S. T., Dudek, D. M., Chen, J., Chitaphan, C.
and Full, R. J. (2006). Dynamics of geckos running
vertically. J. Exp. Biol.
209,260
-272.
Bhushan, B. (2002). Introduction to Tribology. New York: John Wiley and Sons.
Bonser, R. H. C. (2000). The Young's modulus of ostrich claw keratin. J. Mater. Sci. Lett. 19,1039 -1040.[CrossRef]
Bonser, R. H. C. and Purslow, P. P. (1995). The Young's modulus of feather keratin. J. Exp. Biol. 198,1029 -1033.
Campolo, D., Jones, S. D. and Fearing, R. S. (2003). Fabrication of gecko foot-hair like nano structures and adhesion to random rough surfaces. In IEEE Nano 2003 Aug 12-14, vol. 2, pp.856 -859. San Francisco: IEEE. doi:10.1109/NANO.2003.1231049 .[CrossRef]
Creton, C. and Leibler, L. (1996). How does tack depend on contact time and contact pressure? J. Polym. Sci. B 34,545 -554.[CrossRef]
Dahlquist, C. A. (1969). Pressure-sensitive adhesives. In Treatise on Adhesion and Adhesives. Vol.2 (ed. R. L. Patrick), pp.219 -260. New York: Dekker.
Fakley, M. (2001). Smart adhesives. Chem. Ind. 21,691 -695.
Fraser, R. D. B. and Parry, D. A. D. (1996). The molecular structure of reptilian keratin. Int. J. Biol. Macromol. 19,207 -211.[Medline]
Frisch-Fay, R. (1962). Flexible Bars. Washington DC: Butterworths.
Full, R. J. and Koditschek, D. E. (1999). Templates and anchors: neuromechanical hypotheses of legged locomotion on land. J. Exp. Biol. 202,3325 -3332.[Abstract]
Gay, C. (2002). Stickiness - some fundamentals
of adhesion. Integr. Comp. Biol.
42,1123
-1126.
Gay, C. and Leibler, L. (1999). Theory of tackiness. Phys. Rev. Lett. 82,936 -939.[CrossRef]
Geisler, B., Dittmore, A., Gallery, B., Stratton, T., Fearing, R. and Autumn, K. (2005). Deformation of isolated gecko setal arrays: bending or buckling? 2. Kinetics. Int. Comp. Biol. 44,557 .
Glassmaker, N. J., Jagota, A., Hui, C. Y. and Kim, J. (2004). Design of biomimetic fibrillar interfaces: 1. Making contact. J. R. Soc. Interface 1, 1-11.
Hansen, W. and Autumn, K. (2005). Evidence for
self-cleaning in gecko setae. Proc. Natl. Acad. Sci.
USA 102,385
-389.
Hui, C. Y., Glassmaker, N. J., Tang, T. and Jagota, A. (2004). Design of biomimetic fibrillar interfaces: 2. Mechanics of enhanced adhesion. J. R. Soc. Interface 1, 12-26.
Irschick, D. J., Austin, C. C., Petren, K., Fisher, R., Losos, J. B. and Ellers, O. (1996). A comparative analysis of clinging ability among pad-bearing lizards. Biol. J. Linn. Soc. Lond. 59,21 -35.[CrossRef]
Jagota, A. and Bennison, S. (2002). Mechanics
of adhesion through a fibrillar microstructure. Integr. Comp.
Biol. 42,1140
-1145.
Meine, K., Kloss, K., Schneider, T. and Spaltmann, D. (2004). The influence of surface roughness on the adhesion force. Surf. Interface Anal. 36, 694.[CrossRef]
Persson, B. N. J. (2003). On the mechanism of adhesion in biological systems. J. Chem. Phys. 118,7614 -7621.[CrossRef]
Persson, B. N. J. and Gorb, S. (2003). The effect of surface roughness on the adhesion of elastic plates with application to biological systems. J. Chem. Phys. 119, 11437.[CrossRef]
Persson, B. N. J., Albohr, O., Tartaglino, U., Volokitin, A. I. and Tosatti, E. (2005). On the nature of surface roughness with application to contact mechanics, sealing, rubber friction and adhesion. J. Phys. Condens. Matter 17, R1-R62.[CrossRef]
Pocius, A. V. (2002). Adhesion and Adhesives Technology: An Introduction (2nd edn). Munich: Hanser Verlag.
Ruibal, R. and Ernst, V. (1965). The structure of the digital setae of lizards. J. Morphol. 117,271 -294.[CrossRef][Medline]
Russell, A. P. (1975). A contribution to the functional morphology of the foot of the tokay, Gekko gecko (Reptilia, Gekkonidae). J. Zool. Lond. 176,437 -476.
Russell, A. P. (1986). The morphological basis of weight-bearing in the scansors of the tokay gecko (Reptilia: Sauria). Can. J. Zool. 64,948 -955.
Russell, A. P. (2002). Integrative functional
morphology of the gekkotan adhesive system (Reptilia: Gekkota).
Integr. Comp. Biol. 42,1154
-1163.
Scherge, M. and Gorb, S. N. (2001). Biological Micro- and Nanotribology: Nature's Solutions. Berlin: Springer.
Schleich, H. H. and Kästle, W. (1986). Ultrastrukturen an gecko-zehen (Reptilia: Sauria: Gekkonidae). Amphib. Reptil. 7,141 -166.
Simmermacher, G. (1884). Haftapparate bei wirbeltieren. Zool. Garten 25,289 -301.
Sitti, M. and Fearing, R. S. (2003). Synthetic gecko foot-hair micro/nano structures as dry adhesives. J. Adhesion Sci. Technol. 17,1055 -1073.[CrossRef]
Spolenak, R., Gorb, S. and Arzt, E. (2005). Adhesion design maps for bio-inspired attachment systems. Acta Biomater. 1,5 -13.[Medline]
Stork, N. E. (1983). A comparison of the adhesive setae on the feet of lizards and arthropods. J. Nat. Hist. 17,829 -835.[CrossRef]
Tong, T., Zhao, Y., Delzeit, L., Majidi, C., Groff, R. E., Reddy, P., Majumdar, A., Kashani, A. and Meyyappan, M. (2005). Compressive properties of dense vertically aligned multi-walled carbon nanotube arrays. In NANO2005 ASME Integrated Nanosystems: Design, Synthesis & Applications. September 14-16, 2005. Berkeley, California, USA.
Wainwright, S. A., Biggs, W. D., Currey, J. D. and Gosline, J. M. (1982). Mechanical Design in Organisms. Princeton: Princeton University Press.
Williams, E. E. and Peterson, J. A. (1982).
Convergent and alternative designs in the digital adhesive pads of scincid
lizards. Science 215,1509
-1511.
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