Journal of Experimental Psychology:
Human Perception and Performance
1991, Vol. 17. No. 2, 315-322
Copyright 1991 by the American Psychological Association, Inc.
0096-1523/91/$3.00
Grasping Tau
G. J. P. Savelsbergh
H. T. A. Whiting
Faculty of H u m a n Movement Sciences, Free University
Amsterdam, The Netherlands
University of York, Heslington, York, England
R. J. Bootsma
Faculty of Human Movement Sciences, Free University, Amsterdam, The Netherlands
In the present study a direct manipulation of the optical expansion pattern was carded out. What
happens to the timing of the grasp movements involved in catching a ball when optical expansion
information is not veridically provided? By using 2 luminescent balls of constant size and a
luminescent ball that could change its diameter during flight, it was possible to manipulate the
rate of optical expansion directly. The results of 2 experiments (binocular vision in Experiment
l and monocular vision in Experiment 2) showed that the time of the maximal closing velocity
of the hand--which conforms to the prediction if Ss use retinal expansion information--was
later for the deflating ball than for the balls of constant size. Adjustments to the aperture of the
hand in response to the different ball sizes, especially the adjustment of the hand to the deflating
ball (even though Ss were not aware that the ball was deflating during its approach), point to a
finely attuned perception-action coupling.
Schiff, Caviness, and Gibson (1962) demonstrated that an
optically expanding shadow on a white screen resulted in
defensive reactions in diverse species of animals (apes, crabs,
and chickens; see also Schiff, 1965). Later, Bower, Broughton,
and Moore (1970) reported similar effects in 10-day-old babies
when a solid object was made to approach them, giving rise
to optical expansion--the "looming" effect. Schiff and Detweiler (1979) extended the scope of these earlier studies by
using a filmed, animated approach of a black form. Subjects
were told that at a particular stage of its trajectory the approaching object would disappear. Subjects were required to
indicate (by pressing a button) when they thought the object
would have reached them had it continued on the same
trajectory. Several background manipulations were introduced to provide enhanced distance or distance-change information. None of the background manipulations used was
found to influence the accuracy of judgments in relation to
the two-dimensional blank terrain. On the basis of these
findings, Schiffand Detweiler (1979) concluded that observers
can and do use two-dimensional time-to-contact information
to estimate impact time. With respect to the latter study,
however, it has to be stressed that the task given to subjects
was that of a perceptual judgment alone, because they were
not required to carry out actions more complex than pressing
a button. In addition, because of the early curtailment of the
projection, no information on the last 2 s of the moving
object's trajectory was available to subjects. To set the stage
for our experiments, it is necessary to comment further on
two important issues stemming from the experiment of Schiff
and Detweiler (1979).
First, we discuss the use of a button-pressing response.
Obtaining accurate information about visual timing on the
basis of button-pressing responses was recently questioned by
Bootsma (1988, 1989). In his study, subjects were required
(a) to strike with a table tennis bat and a squash ball dropped
along a fixed path, (b) to release an artificial arm to hit a
similar ball, and (c) to press a button when the ball reached
the point of contact. All three actions were carded out under
similar optic flow patterns. The results indicated that the
variability of the moment of initiation was considerably larger
under the button-pressing condition than under the artificialarm condition, which again was larger than that under the
natural-arm condition. The more the required action was
separated from a natural perception-action coupling, the less
precise the timing response was found to be; this finding is
corroborated by the results of McLeod, McLaughlin, and
Nimmo-Smith (1986).
Second, we discuss the absence of information in the last 2
s of approach of an expanding optical form (also the case in
the McLeod & Ross, 1983, study). Such information might
be very important in those tasks such as catching a ball in
which subjects have to carry out an action to actually intercept
an approaching object. This is confirmed in Alderson, D. L.
Sully, and H. G. Sully's (1974) analysis of ball catching, in
which the grasp phase of the catching action (a timing problem) occurs some 40 ms prior to contact. In the same vein,
an even more valid paradigm (in the sense that more than
one velocity was studied) was provided by Lee, Young, Reddish, Lough, and Clayton (1983) in their investigation of
visual timing in hitting an accelerating ball. The experimental
design (a falling football that had to be punched away) was
such that to perform the subactions involved (e.g., extension
of knee and elbow) information occurring in approximately
the last 250 ms of ball flight had to be used. The results were
consistent with subjects' use of visual information occurring
in the last 50-135 ms.
Experiment 1 is motivated both by the limitations of the
aforementioned experiments and the necessity to clarify fur-
Correspondence concerning this article should be addressed to
G. J. P. Savelsbergh, Faculteit der Bewegingswetenschappen, Van der
Boechorststraat 9, 1081 BT Amsterdam, The Netherlands.
315
316
G.J.P. SAVELSBERGH, H. T. A. WHITING, AND R. J. BOOTSMA
ther the confounding explanations for the explanatory value
of direct versus indirect theories of perception.
In a similar type of study, albeit one that used a computer
simulation methodology, Todd (198 l) demonstrated that subjects could reliably discriminate arrival times of objects of
different sizes starting from different positions with different
velocities directly on the basis of two-dimensional information.
At about the same time that Schiff was extending his work
(Schiff & Detweiler, 1979) on optical expansion, Lee (1976,
1980) demonstrated that the inverse of the relative dilation
rate of an approaching object--an optical variable that he
denoted by tau--constituted a first-order two-dimensional
source of information that specified the time to contact. In
the ensuing years, Lee and his co-workers sought to confirm
the efficacy of the time-to-contact variable in a series of diverse
and elegant studies. Thus, Lee and Reddish (1981) showed
how such a variable might be used to explain the timing of
diving gannets' folding their wings. Lee, Lishman, and Thomson (1982) followed up this study by demonstrating the efficacy of a similar control parameter in regulating gait during
the run-up phase of the long jump, whereas Warren showed
the role of this optical variable in the visual control of step
length during running over irregular terrain (Warren, Young,
& Lee, 1986). Lee et al. (1983) reported on the sequencing of
behavior involved in jumping up to punch a falling ball,
which provided further evidence for the explanatory power of
the optical variable tau. More recently, Bootsma (1988;
Bootsma & van Wieringen, 1990) invoked a similar explanation in the control of directed striking of a table tennis ball,
and Sidaway and his co-workers (Sidaway, McNitt-Gray, &
Davis, 1989) demonstrated that preparatory muscle activation
prior to impact landing from different heights is triggered at
a specific tau margin. For the regulation of gait in horses'
jumping of obstacles, Laurent, Dinh Phung, and Ripoll (1989)
demonstrated that the retinal expansion pattern of the obstacle is used by the riders.
The studies addressed here provide a catalog of evidence in
support of the explanatory power of a direct-perception explanation of control of timing in a variety of ecologically
appropriate skills. They constitute a challenge to classical
information-processing explanations, which suggest that such
actions as those reported here are driven by "a complex
predictive system which takes into account any available
information about the ball's current position, velocity, acceleration, rate of change of acceleration and so on" (Lee &
Young, 1985). Such a complex system, as Lee and Young
suggest, would entail unnecessary delays in using the information as well as oversensitivity to noise and is thus unlikely
to have evolved. A better system, they suggest, is robust rather
than overly refined and takes advantage of the most reliable
and rapidly available information--to them the inverse of the
relative rate of optical expansion.
Although the logic of Lee and Young's argument is fairy
convincing and the evidence they produce is rather compelling, it has to be pointed out that no one has directly manipulated the optical expansion pattern while evaluating the
consequences in terms of the delayed/accelerated initiation
of patterns of action. Computer simulation (Todd, 1981) and
discrimination studies (e.g., Schiff& Detweiler, 1979) are not
sufficient to evaluate the proposed continuous coupling of
perception and action in, for example, the task of catching
(Lee & Young, 1985). By the same token, demonstrating that
the timing of movement sequences is compatible with the use
of the optical variable tau (Lee & Reddish, 1981; Lee et al.,
1983) is not sufficient to prove that the relative rate of dilation
is responsible for such timing, because the expansion pattern
has never been experimentally manipulated. Though we agree
that the circumstantial evidence resulting from the aforementioned studies is convincing, the direct demonstration of Lee's
proposed perception-action coupling in catching is still
awaited; Experiment 1 set out to accomplish this. More
specifically, it attempts to provide an answer to the following
question: What happens to the timing of the grasp movements
involved in catching an approaching ball when optical expansion information is not veridically provided?
In an attempt to answer this question, we used a paradigm
that, with a repeated measures design, compares the behavior
of subjects who were required to catch three types of approaching balls (a small ball, a larger ball, and a ball that decreased
in size as it approached). ~ If subjects do indeed gear their
catching actions to time-to-contact information derived from
the relative expansion pattern of the ball, two important
predictions can be made. First, the adjustments of the hand
aperture ought to be tuned accurately to the changing ball
size (including the deflating ball). Second, the time of appearance of the fingers' maximal closing velocity ought to be later
for the deflating ball than for the other two ball sizes.
Experiment 1
Method
Subjects
Subjects were 10 undergraduate women 19-26 years of age who
reported normal or corrected-to-normal vision and who were naive
to the purpose of the experiment. Subjects were paid for their participation.
Apparatus
Three balls with different diameters were used as catching objects.
Two of these were relatively
foam-plastic balls 5.5 cm and 7.5
cm in diameter, respectively, that were enclosed in a tight-fitting
balloon painted with luminous paint. A third ball could be made to
change its diameter from 7.5 cm to 5.5 cm during flight. This was
achieved by using a luminous balloon that enclosed another relatively
rigid foam-plastic ball 5.5 cm in diameter. This ball could be inflated
to a 7.5-cm diameter prior to release and allowed to deflate during
its trajectory until it formed a tight "skin" around the enclosed ball
at the moment it arrived at a subject's hand.
For each trial, one of these luminescent balls was fastened to the
end of an aluminum pendulum 3.92 m in length that was hinged to
a point on the ceiling of the laboratory. When raised from its resting
' The idea of using an inflating or shrinking ball in time-to contact
research was put forth by Beck (1986).
GRASPING TAU
position, the pendulum could be held in its new position by an
electromagnet. The horizontal distance between the magnet and a
subject's hand was 2.48 m, which resulted in a speed of 2.4 m/s. A
subject sat in a chair with her right arm secured to a black metal
armrest, which left the catching hand free. The armrest was fixed to
the table and could be adjusted to the length of the lower arm (see
Figure 1).
A multi-infrared light-emitting diode (LED) control unit (Den
Brinker, Krol, & Zevering, 1985) consisting of an Apple II+ microcomputer coupled to a Selcom 413-3 camera was available for data
registration. With this system, we could register the position of four
infrared light sources (LEDs) fixed to the lower end of the pendulum,
the first thumb phalanx, and the first finger phalanx of the right hand.
The position signal was sampled with a frequency of 200 Hz.
To control the viewing period, subjects wore liquid crystal spectacles,2 which could be made to change from opaque to clear by an
electric signal generated as the pendulum was released by the electromagnet. The rise and decay times for the crystals were less than 4 ms.
The spectacles remained clear for a period of 2 s and became opaque
again following a signal generated at the moment the ball reached a
subject's hand. The experiment was carried out in a totally dark
room.
Optical Expansion of the Deflating Balloon
To establish that the deflating balloon resulted in a pattern of
optical expansion different from a ball of constant physical size, we
recorded ball flights by means of a video camera with the lens situated
at eye level. Analysis of the two-dimensional expansion pattern on
the monitor screen was carried out with a video position analyzer
(VPA 1000) that allowed the diameter of the ball to be measured
frame by frame (40 ms) during its approach. The expansion patterns
of the deflating ball (B) and a ball of constant size (A) are shown in
Figure 2. This analysis confirms that the deflating ball would result
in a different optical expansion pattern than would a ball of constant
physical size.
Procedure
To familiarize subjects with the equipment, the experimenter
released the pendulum five times. This was followed by 50 experimental trials in the totally dark room. Between each trial the room
317
1200
A
1000
800 '
¢0
•~
600 -
IZ
I~.
X
nl
400 -
200
'
0
=
-1500
-1000
,
-500
0
"rime betore contact (ms)
Figure 2. The relative expansion pattern (on a video screen) of a
ball of constant size (A) and the deflating ball (B).
light went on to "load" the luminescent paint. During this time the
spectacles remained opaque. The two rigid balls were each used 20
times and the deflating ball was used 10 times in an order randomized
over trials. Subjects wore white-noise headphones to prevent anticipation resulting from any sound from the deflating ball(oon).
Data Analys&
The position data were filtered with a recursive second-order
Butterworth filter with a cutoff frequency of 8 Hz. The filter was
applied twice to negate the phase shift.
Dependent Variables
We used two criteria in selecting the dependent variables for
analysis of the grasping action. First was the need to check whether
the manipulation of ball size (large and small) conformed with
predictions made on the basis of grasping studies (Jeannerod, 1981,
1984; Marteniuk, Mackenzie, & Leavitt, 1990; Von Hofsten &
Ronnqvist, 1988). For this purpose, the following dependent variables
were chosen: maximal aperture of the hand, moment of occurrence
of the maximal aperture in time, movement time of the grasping
component, aperture of the hand at the moment of catch, and
maximal closing velocity of the hand. The second criterion was the
need to select variables that might be sensitive to changes brought
about by the deflating ball and hence to provide information relevant
to the predictions made at the end of the introduction. The following
dependent variables were selected for this purpose: time of appearance
of the maximal closing velocity and the size of the aperture of the
hand.
Description of Dependent Variables
Figure 1. The position of the LEDs on the hand and on the
pendulum and attachment of the balls to the pendulum. (The horizontal distance between the hinge of the pendulum and a subject's
hand was 1.12 m; the hand was fixated in an armrest. A subject's
head was virtually in line with the catching hand and the approaching
ball.)
Time of initiation of the grasp. This variable denotes the time
between the release of the pendulum by the magnet (spectacles
become clear) and the initiation of the grasp (defined as the moment
of maximal opening of the hand).
Movement time. This variable denotes the elapsed time between
the initiation of the grasp and the moment of ball-hand contact
(catch).
2 We are grateful to the National Aerospace Laboratory NLR,
Amsterdam, for the loan of the liquid crystal spectacles.
318
G.J.P. SAVELSBERGH, H. T. A. WHITING, AND R. J. BOOTSMA
Table 1
Means and Standard Deviations for the Dependent Variables
(Experiment 1)
Ball
Dependent variable
Time of initiation of
the grasp
SD
Movement time
SD
Time of eatch
SD
Maximal dosing
velocity
SD
Large
Small
Deflating
1,575
68
1,580
65
1,585
67
140
51
154
48
153
51
1,716
39
1,738
36
1,739
36
-37
18
-48
15
-50
16
Time of maximal
closing velocity
-41
-42
-36
10
11
14
Note. Values for maximal closing velocity are in centimeters per
second. All other values are in milliseconds. The large ball was 7.5
cm in diameter; the small ball was 5.5 cm in diameter. The deflating
ball changed from 7.5 to 5.5 cm in diameter. The significant difference
in the "time of catch" is because the large ball, by virtue of its greater
diameter, reached the hand earlier than the small ball. Minus signs
indicate that the appearance of the time of maximal closing velocity
is before ball-hand contact.
vs. deflating) analysis of variance (ANOVA) carried out for
the means and standard deviations of each of the dependent
variables, with a repeated measures design on the last variable.
We found a significant main effect for the means of the
ball-size variable for the following dependent variables: time
of catch, F(2, 18) = 24.94, p < .001; maximal closing velocity,
F(2, 18) = 12.46, p < .001. A 6% significance level occurred
in movement time, F(2, 18) = 3.24, p = .06, and time of
maximal closing velocity, F(2, 18) = 3.25, p = .06. For the
standard deviation, only the time of maximal closing velocity
reached a 5% significance level, F(2, 18) --- 3.50, p = .05.
With respect to the hand aperture, we found a significant
effect at the moment of initiation, F(2, 18) = 21.15, p < .001;
maximal closing velocity, F(2, 18) = 26.73, p < .001; and
time of catch, F(2, 18) -- 22.19, p < .001. We found no
significant effects for the standard deviations. Post hoc Newman-Keuls analyses indicated a number of significant differences.
SD
Maximal closing velocity. This variable denotes the maximal
closing velocity of the hand.
Time of appearance of maximal closing velocity.
(Maximal) aperture of the hand. This variable denotes the (maximal) distance between the LEDs on the thumb phalanx and the
finger phalanx.
Results
The results are reported in Tables 1 and 2 together with the
results of a separate three-variable (ball size: large vs. small
Table 2
Means and Standard Deviations of Hand Aperture at
Different Times
Ball
Hand aperture time
Initiation
SD
Maximal closing velocity
SD
Time of eatch
Large
8.84
0.71
Small
8.33
0.74
Deflating
8.80
0.71
7.38
0.80
6.30
0.68
6.60
0.76
6.22
4.68
5.00
1.1
1.0
1.1
Note. All values are in centimeters. The large ball was 7.5 cm in
diameter; the small ball was 5.5 cm in diameter. The deflating ball
changed from 7.5 to 5.5 cm in diameter.
SD
Differences Between Large and Small Balls
We found no significant differences between the intraindividual standard deviations on any of the variables. Significant
differences were apparent between the mean scores of the
large ball and the small ball for several dependent variables.
The small ball showed a smaller maximal hand aperture, a
longer movement time, a smaller hand opening at the time
of catch, and a higher maximal closing velocity than the large
ball (all p < .05).
The larger hand aperture for the large ball was in accordance
with a number of recent findings in the literature on reaching
and grasping movements (e.g., see Jeannerod, 1981; Von
Hofsten & Ronnqvist, 1988). As in Von Hofsten and Ronnqvist's (1988) experiment, the difference in hand aperture for
the small and large balls was much less than the difference in
size of the two balls. The shorter movement time for the large
ball is a reflection of the shorter closing distance the fingers
needed to cover for the large ball than for the small ball.
Similarly, the significantly higher maximal closing velocity
for the small ball confirms the logical predictions. The higher
velocity and longer movement time for the small ball are
complementary consequences of the greater distance the fingers have to travel to catch the small ball. The differences in
hand opening at the moment of catch and at the moment of
maximal closing velocity reflect differences in the size of the
balls and confirm other reported findings of adjustments to
hand movement in relation to the particular size of objects
(Jeannerod, 1981; Von Hofsten & Ronnqvist, 1988). The fact
that the hand aperture is larger than needed indicates a
strategy proposed by Wing, Turton, and Fraser (1986; see also
Wallace, Weeks, & Kelso, 1990): Adults opened their hand
more when a fast reach rather than a slow reach was carried
out to a static object. The results meet the expectations
stemming from the findings in the literature. They give confidence that there was nothing untoward in the paradigm we
used, and at the same time they provide the baselines for the
deviations to be reported when a deflating ball is used.
GRASPING TAU
Differences Between the Deflating Ball and Balls of
Constant Size
Significant differences were found between the deflating
ball and the large ball on the mean scores of several dependent
variables. In relation to the data obtained for the large ball,
the deflating-ball condition resulted in a longer movement
time, a smaller hand aperture at the moment of catch, a
higher maximal closing velocity, and a later appearance of
the maximal closing velocity (all ps < .05). In accordance with
the discussion of the results of the differences between the
large and the small ball, these findings confirm that the
deflating ball is treated as a ball that is smaller than the large
ballminformation that is not available until it is actually
under way. A perceptually noticeable difference in its rate of
optical expansion leads to an adjustment in the action pattern.
The longer movement time and higher maximal closing velocity reflect (as was the case with the small ball) the longer
distance that is involved in catching the deflating ball. We
found no statistically significant differences in hand-aperture
size between the deflating ball and the small ball at the
moment of catch. On other dependent variables, however,
the significant differences found between the deflating ball
and the small ball indicate that the two balls were not treated
alike during the earlier parts of their trajectories.
The maximal hand aperture for the deflating ball was
significantly larger than for the small ball and statistically
similar to the maximal hand aperture under the large-ball
condition. In agreement with Jeannerod's findings (1981,
1984), we found no differences in the time of appearance of
the maximal hand aperture. This finding suggests that subjects
probably decide early on the aperture size necessary for a
successful catch and allow a sufficient tolerance band for the
different ball sizes. We found no differences in standard
deviations for either of the dependent variables, which indicates that subjects used a consistent strategy in this respect.
The most important finding in the context of the predictions
made is the later appearance of the time of maximal closing
velocity for the deflating ball in comparison to the other balls.
The later appearance of this dependent variable indicated that
the deflating ball and the consequent less relative retinal
expansion (as opposed to an approaching ball of constant
physical size) resulted in an adjustment to the timing of the
grasp.
When the hand apertures (see Table 2) at the time of
initiation, at the moment just before the catch, and at the
moment of the actual catch are compared, adjustments to
accommodate the differing sizes of all three balls is apparent.
We found a significant difference between the deflating-ball
and the small-ball conditionsmbut not between the deflatingball and the large-ball conditions--at the moment of initiation. We found significant differences between all balls at the
moment of maximal closing velocity, and we found a significant difference between the deflating-ball and the large-ball
conditionsmbut not between the deflating-ball and the smallball conditions--at the moment of catch. Figure 3a shows the
mean maximal aperture over the last 200 ms, confirming this
statement. These findings indicate that adjustments to the
319
hand aperture were still being made up to the last moment
before ball-hand contact.
In this respect the visuomotor delay time is interesting. By
plotting the standard deviation of the hand aperture over the
last 200 ms, we get an indication of the visuomotor delay
times involved. The interesting statistic in this respect is the
point of minimal variance. As Figure 3b indicates, a visuomotor delay time of about 100 ms before ball-hand contact
seems to be the case for all ball sizes. This result is in
agreement with the findings of other researchers (Bootsma &
van Wieringen, 1990; Lee et al., 1983).
Discussion
Although the results provided here confirm our predictions
(made in the introduction) on the basis of subjects' use of
time-to-contact information directly specified by optical expansion of the ball, this is not categorical proof that subjects
do use such information. The nagging doubt remains that the
use of two eyes provides other sources of information that
might be used equally well (or additionally). For example, in
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5'
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-180
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-140
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-1 0
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-60
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-20
20
Time before contact (ms)
1.3
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b
1.2'
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-220
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-180
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-100
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20
Time before contact (ms)
Figure3. (a) Adjustments to the mean aperture of the hand for the
large ball (L), the small ball (S), and the deflating ball (B) in the last
200 ms in Experiment I (sampling 200 Hz); (b) the standard deviation
for all three ball sizes in the last 200 ms in Experiment 1 (sampling
200 Hz).
320
G.J.P. SAVELSBERGH, H. T. A. WHITING, AND R. J. BOOTSMA
a series of experiments Jones and Lee (1981) showed that
performance with binocular vision is superior to performance
with monocular vision in a variety ofvisuomotor tasks. When
vision with two eyes is provided, an image of the bail is
projected on both retinas. The distance between these two
images increases when the ball approaches and decreases when
the ball goes away, thus providing subjects with a potential
source of distance information (Regan, 1986). In principle,
therefore, it is possible for catchers to compute time to contact
on the basis of this distance information and estimated velocity (the velocity in all trials was the same, which could lead
to some experience effect).
To obviate this alternative indirect explanation, we need to
run a second experiment in which this binocular source of
information is removed, that is, in which subjects are required
to perform monocularly. Under the latter condition, time to
contact specified by optical expansion is still available, and
thus the same predictions as for the binocular condition of
Experiment 1 apply.
Table 3
Subjects" Judgments With Respect to the Kind of Ball Used
in the ControlAspect of Experiment 2 (n = 5)
Trial
Subject
1
2
3
4
5
Large
ball
Large
Large
Large
Large
Large
Small
ball
Small
Small
Small
Small
Small
Deflating
ball(oon)
Small
Small
Small
Large
Small
Large
ball
Large
Large
Large
Large
Large
Ball(oon)
not deflating
Large
Large
Large
Large
Large
were almost totally in agreement (only Subject 4 referred to
the deflating ball as large; the other subjects referred to it as
small). None of the subjects referred to the peculiar behavior
of the deflating ball. When the bail(oon) was not deflating, all
subjects recognized it as a large ball, and when it was deflating
(with the exception of Subject 4), they recognized it as a small
ball.
Experiment 2
Time of Appearance of Maximal Closing Velocity
The second experiment was a replication of the methodology used in Experiment 1, with the binocular condition being
replaced by a monocular condition.
Method
Subjects
Subjects were 5 undergraduate women 19-24 years of age who
reported normal or corrected-to-normal vision and who were naive
to the purpose of the experiment. None of the subjects participated
in the first experiment; they were paid for their participation here.
Apparatus, Dependent Variables, Data Collections,
Data Analyses, and Procedure
These were the same as in Experiment 1. Only one change was
made with respect to the liquid crystal spectacles: To control monocular vision, the spectacles were made to change from opaque to clear
for one eye by an electrical signal generated as the pendulum was
released by the electromagnet. Subjects underwent 50 trials: 25 in
which the ball was seen by the left eye only, and 25 in which (10 with
the large ball, 10 with the small ball, and 5 with the deflating ball)
the ball was seen by the right eye only.
We introduced an additional control into this experiment to check
the accuracy of subjects' statements (in Experiment l) that they were
not aware of the deflating bail. To this end, subjects were asked after
the experiment to make visual judgments about the balls without
making a catching attempt. Five trials were conducted: large ball,
small ball, deflating ball(oon), large ball, and ball(oon) not deflating.
Results
Visual Judgment About Balls
The control aspect of Experiment 2 produced the data
presented in Table 3. As can be seen, subjects' judgments
The results for this dependent variable are reported in Table
4. Again, we found differences between the deflating ball and
the balls of constant size. The time of appearance of the
maximal closing velocity for the deflating ball was later than
for the small and large bails.
A two-variable (eyes: left vs. right) by three-variable (ball
sizes: large vs. small vs. deflating ball) ANOVA with repeated
measures on the last two variables showed a main effect for
ball size, F(2, 8) = 7.47, p < .015. Newman-Keuls post hoc
comparisons showed significant differences between the deflating ball and the two other bails but not between the large
bail and the small bail (ps < .05). No significant main effects
were found for the eyes' variable, and there were no significant
interactions.
Adjustment of the Hand Aperture
Figure 4a shows the hand adjustments for the last 200 ms.
As in Experiment 1, we found the fine tuning of the hand
aperture to the ball size. Figure 4b shows the differences in
hand aperture between the large ball and the deflating ball
Table 4
Means and Standard Deviationsfor the Time of Appearance
of the Maximal Closing Velocityfor the Left Eye and the
Right Eye and for All Ball Sizes
Ball
Vision
Right eye
Left eye
Total
Large
-49.9
-42.9
Small
-37.7
-41.7
Deflating
-25.9
-21.0
-46.4
-39.7
-23.5
24
16
12
Note. Minus signs indicate that the appearance of the maximal
closing velocity is before ball-hand contact.
SD
GRASPING TAU
those found in Experiment 1 for the deflating ball (120 ms)
and the large ball (125 ms) but different for the small ball (40
ms). In addition the standard deviation decreases closer to
ball-hand contact, which was not the case in Experiment 1.
In summary, we replicated the findings of Experiment 1 in
this experiment, although the differences in the time of appearance of the maximal closing velocity are somewhat exaggerated under the monocular condition.
a
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4'
General Discussion
3
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i
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-180
-140
-100
-60
-20
Time before contact (ms)
E
0
0.5
P
0.4'
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b
B-S xx
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-220
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u
u
-180
-140
-100
-60
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20
Timebeforecontact(ms)
1.6
E
O
1.4
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B
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1.2
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1.0
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0.8
-220
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-1
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u
-100
-60
u
-20
Time before contact (ms)
Figure 4. (a) Adjustments to the mean aperture of the hand for the
large ball (L), the small ball (S), and the deflating ball (B) in the last
200 ms in Experiment 2 (sampling 200 Hz); (b) the differences in
hand aperture between the large ball and the deflating ball (L - B)
and between the deflating ball and the small ball (B - S); (c) the
standard deviation for all three ball sizes in the last 200 ms in
Experiment 2 (sampling 200 Hz).
and between the deflating ball and the small ball. At the
beginning of the flight the deflating ball (as might be expected)
leads to hand apertures closer to the large ball; in the last 150
ms it leads to apertures closer to the small ball. Figure 4c
shows the standard deviation of the hand aperture for the
three ball sizes. The points of minimal variance are similar to
The findings of the studies presented here, in which the
optical variable tau was experimentally manipulated, are consistent with subjects' use of relative expansion information on
which to base their catching actions. Subjects adjusted their
action to a deflating ball even though they were apparently
unaware (by verbal report in Experiment l and visual-judgment report in Experiment 2) of its peculiar behavior. Not
only were they successful in catching the deflating ball, but
their actions were finely tuned to its size change. Several
reasons for the latter fact exist. As a result of the subtle
manipulation of the expansion and the low approach velocity
of the balls, the available time window was long enough for
subjects to make a catch. Relative expansion, albeit less than
that from a ball with a constant physical size, was still available
(Figure 2). Thus, the artificially manipulated relative expansion (i.e., not synchronized to the ball approach) still provides
enough information to facilitate catching within the time
constraints (time window) available.
The results obtained under the binocular condition of Experiment l are open to explanations other than subjects' using
optical expansion information to make their time-to-contact
judgments. Nevertheless, the use of a monocular condition in
Experiment 2, which led to similar delay times (albeit with a
different group of subjects), suggests that binocular information (other than optical expansion information) does not
facilitate catching performance under the conditions of the
experiments reported here. The use of different ball sizes
together with a deflating ball requires that subjects make
subtle changes in their grasping actions if they are to achieve
success, some of these changes late in the bali's flight. The
fact that subjects were able to attune their actions to such
perceptual nonveridical changes argues strongly for the steering effect of environmental information rather than some
preprogrammed catching action actuated at some particular
moment. This finely attuned perception-action coupling
manifests itself most clearly in the adjustments of the hand
aperture to the deflating ball (see Figures 3a, 4a, and 4b). The
subjects do not know and are apparently not aware that the
ball is deflating during its approach. (By the time the ball is
caught, there are no detectable differences between the deflating ball and the small ball.) Despite this, subjects adjusted
their hand actions to meet the changing demands. As Lee and
Young (1985) hinted, the timing of the catching action is
under continuous visual control such that adjustments to the
catching hand are apparent even at a relatively short time
interval prior to ball-hand contact. The fact that the standard
deviations of hand aperture become smaller when the ball
comes nearer to the hand suggests that the visual information
322
G.J.P. SAVELSBERGH, H. T. A. WHITING, AND R. J. BOOTSMA
becomes more precise as contact approaches (see also Lee &
Young, 1985). From the experiments reported here, however,
it is not clear to what stage in the trajectory of the ball that
optical expansion information can be used to adjust the hand
aperture. The results of Experiment 1 showed increases in
standard deviation between 110 and 0 ms before contact,
which gives an indication of the visuomotor delay time and
the inability to modify accurately the grasping action during
this time window. In contrast, Experiment 2 showed a different pattern: decreases in the standard deviation within the last
100 ms. Ongoing research is already focusing on this apparent
anomaly.
Overall, the findings of our experiments confirm that information occurring in the last 200 ms of ball flight before
contact is indeed used to tune the catching action and that
the inverse of the relative rate of retinal expansion provides
accurate time-to-contact information, as proposed by Lee and
his co-workers (1976, 1980, 1982, 1983).
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Received October 23, 1989
Revision received August 15, 1990
Accepted August 16, 1990 •