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| Volume 4, Number 7, Article 5, Pages 575-584 |
doi:10.1167/4.7.5 |
http://journalofvision.org/4/7/5/ |
ISSN 1534-7362 |
Representational momentum in perception and grasping: Translating versus transforming objects
Anne-Marie Brouwer |
Max Planck Institute for Biological Cybernetics,
Tübingen, Germany |
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Volker H. Franz |
Justus-Liebig-Universität Giessen, Allgemeine Psychologie,
Giessen, Germany |
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Ian M. Thornton |
Max Planck Institute for Biological Cybernetics,
Tübingen, Germany |
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Abstract
Representational momentum is the tendency to misremember the stopping point of a moving object as further forward in the direction of movement. Results of several studies suggest that this effect is typical for changes in position (e.g., translation) and not for changes in object shape (transformation). Additionally, the effect seems to be stronger in motor tasks than in perceptual tasks. Here, participants judged the final distance between two spheres after this distance had been increasing or decreasing. The spheres were two separately translating objects or were connected to form a single transforming object (a dumbbell). Participants also performed a motor task in which they grasped virtual versions of the final objects. We found representational momentum for the visual judgment task for both stimulus types. As predicted, it was stronger for the spheres than for the dumbbells. In contrast, for grasping, only the dumbbells produced representational momentum (larger maximum grip aperture when the dumbbells had been growing compared to when they had been shrinking). Because type of stimulus change had these different effects on representational momentum for perception and action, we conclude that different sources of information are used in the two tasks or that they are governed by different mechanisms.
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History
Received November 8, 2003; published July 14, 2004
Citation
Brouwer, A.-M., Franz, V. H., & Thornton, I. M. (2004). Representational momentum in perception and grasping: Translating versus transforming objects.
Journal of Vision, 4(7):5, 575-584,
http://journalofvision.org/4/7/5/,
doi:10.1167/4.7.5.
Keywords
representational momentum, visuomotor, human, grasping, boundary extension
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When observers are asked to indicate the stopping point
of a moving object, they typically indicate some point further forward in the
direction of the (actual or implied) motion. This phenomenon is called
representational momentum (Freyd & Finke, 1984; for a review, see Hubbard, 1995,
2003; for a recent collection of related work,
see Thornton & Hubbard, 2002). In
the first study that showed representational momentum (Freyd & Finke, 1984), observers were presented with three
discrete visual presentations of a rectangle rotating in the picture plane. The
observers were asked to remember the position of the third item and to indicate
whether a fourth rectangle was the same as the third or not. Freyd and Finke
found that the fourth rectangle was more likely to be erroneously judged as
being the same when it was rotated forward in the direction of motion from the
true stopping point, versus the same distance backwards. Since this initial
study, many other examples of forward displacement have been found, using a
variety of stimuli, including single translating objects (Hubbard &
Bharucha, 1988), groups of translating objects
(Finke & Shyi, 1988), depth rotated
novel figures (Munger, Solberg, Horrocks, & Preston, 1999), articulating human figures (Verfaillie
& Daems, 2002), and crowds of human
figures (Thornton & Hayes, 2004).
In addition to implied motion sequences, representational momentum has been
found with displays involving induced motion (Faust, 1990), smooth continuous motion (Hubbard &
Bharucha, 1988; see also Kerzel, 2000), and in static scenes where motion is
only suggested pictorially (Freyd, 1983;
Kourtzi & Kanwisher, 2000).
The ability to find forward displacements across a wide
range of display types led Freyd ( 1987) to
predict representational momentum “for any dimension of continuous
change.” However, almost all of the evidence to date has involved either
actual or implied motion, that is, a change of position over time. Brehaut and
Tipper ( 1996) carried out several experiments
to see whether they could demonstrate representational momentum with a
completely different form of change. They presented participants with objects
that changed brightness over time. Instead of representational momentum, they
found exactly the opposite pattern: When the stimulus changed from dark to
light, participants remembered the last instance of the stimulus as darker then
it actually was and when the stimulus changed from light to dark, they
remembered the last stimulus as being lighter than it was. This finding led
Brehaut and Tipper to conclude that representational momentum might be something
typical for moving, but not necessarily
changing, stimuli.
Several recent studies from our lab appear to be
consistent with this notion. Visual tasks involving growing cubes (Franz,
Bülthoff, Fahle, & Thornton, 2001), expressive faces (Thornton, 1997), deforming objects (Thornton, Vuong,
Knappmeyer, & Bülthoff, 2002), and opening or closing pliers
(Brouwer, Franz, & Thornton, 2003a; Brouwer, Thornton, &
Franz, 2003b) all failed to
provide clear evidence of representational momentum; most of them showed the
opposite pattern. Although these stimuli involved motion of parts of the object,
the overall stimulus did not change position and may be better described as
changing identity or transforming rather than as moving. Previous findings by
Kelly and Freyd ( 1987) also suggest
that representational momentum might be typical for moving rather than for
changing stimuli. Specifically, while they found representational momentum for
coherent changes, such as shrinking (receding) and growing (approaching)
squares, they did not find (strong) representational momentum for less coherent
changes in shape.
The purpose of the present study was to create a
display in which the effects of change in position (translation) and change in
identity (transformation) could be directly compared. To do this we created two
types of stimuli that varied in the degree of transformation while leaving most
other aspects (including the degree of translation) constant. One type of
stimulus consisted of two spheres that moved toward or away from each other; the
other consisted of the same two spheres but the spheres were connected by a bar
to form one single, transforming object (“dumbbells,” see Figure 1). We used a standard probe task to
measure visual representational momentum. For the spheres, being two separately
translating objects, we predict stronger representational momentum than for the
dumbbells, which can be seen as a single transforming object.
Figure 1. Stimuli. A. Dumbbells. B. Spheres. C.
The white outlines indicate the size and position of the simulated haptic
objects (invisible in the actual stimulus), which were exactly the same for the
dumbbells and the spheres.
Previous studies have also suggested that the mode of
response can make a difference in judging the final instance of an object. For
example, Kerzel ( 2003) found stronger
representational momentum when participants indicated the last position of a
translating disk by pointing or by moving a cursor than when they judged the
disc’s position purely visually. In our previous work, when observers were
asked to reach out and grasp the final instance of a transforming object, they
opened their hands wider for growing or opening objects than for shrinking or
closing objects (Brouwer et al., 2003a,
2003b; Franz, Bülthoff, Fahle, & Thornton, 2001). This behavior contrasted with
visual tasks on the same displays, suggesting a possible difference between
perception and action in this context. In the present work, we also asked
participants to grasp the final instance of the spheres or dumbbells to further
explore the differential effect of response mode on representational
momentum.
The stimulus consisted of a sequence of 2D rendered
images of dumbbells ( Figure 1A) or spheres
( Figure 1B), presented on a black background.
The dumbbells and spheres were presented in two separate experiments, to
different groups of participants. In the following, the methods will be
described for the dumbbells. For the spheres, the experiment was exactly the
same except for leaving out the bar that visually connected the two spheres in
the dumbbell stimuli.
General setup and stimuli
Figure 2 shows a
schematic overview of the experimental setup, which involved stereo-computer
graphics (OpenGL, SGI Octane II, and Crystal Eye shutter glasses), two robot
arms (Phantom TM), a monitor, and a mirror. Participants were seated
on a chair and looked down into the mirror through the shutter glasses. The
monitor that was mounted above the mirror presented the stimuli so that they
appeared to be on the left of a horizontal plane, at a distance of approximately
50 cm from the participants’
eyes. Figure 2. Overview of the experimental setup. The
Phantoms were only used in the grasping task.
There were three kinds of (implied) motion of the
dumbbells; increase, decrease, and static. In the conditions
“increase” and “decrease,” we presented participants
three dumbbells in succession. The sequence could either imply an increasing
distance between the spheres or a decreasing distance, in steps of 1 cm. Each
dumbbell was presented for 250 ms, and there was a 250-ms interval in between.
In the condition ”static,” only one pair of dumbbells was shown for
250 ms. We included this condition as a baseline and to check for a general
decrease in remembered size, which appeared to be present in previous studies
(Brouwer et al., 2003a, 2003b;
Hayes & Freyd, 2002; Hubbard, 1996; Franz et al., 2001). The final distance between the
outer edges of the spheres could be either 37 mm or 47 mm (“target
size”). The stimuli were presented blocked for motion type (increase,
decrease, or static). Previous studies have shown that forward displacement can
be more reliably measured under these conditions, probably due to the increased
predictability of the observed sequence (Kerzel, 2002). The order of the blocks was
randomized.
We used the traditional representational momentum probe
task to measure perceptual performance. After the target pair of dumbbells had
disappeared, and a 250-ms interval was presented, an additional pair of
dumbbells was shown for 250 ms. This pair of “comparison” dumbbells
could be either exactly the same as the target, or 2.5-, 5-, 7.5-, or 10-mm
shorter or longer. The participants were asked to watch the whole sequence and
to indicate whether the comparison dumbbell was different from the target by
pressing the appropriate button on the keyboard that they held on their lap.
They were told that the proportion of “different” and
“equal” responses needed not be the same (in fact, the true
proportion of “equal” comparison dumbbells was 0.11), and that the
difference could be very small. The comparison dumbbells remained visible until
the participants responded or until they had been presented for 3 s. In the
latter case, participants received a message that they had been too slow and the
trial was repeated later.
Participants practiced 10 trials at the start of each
block (increase, decrease, and static). After that, they performed (2 target
sizes × 9 comparisons × 8 repetitions =) 144 experimental trials. This
results in a total of (144 × 3 motion types =) 432 perceptual trials for
each participant. No feedback was
given.
During the grasping task, the thumb and the index
finger of the participant’s right hand were attached to two robot arms
(Phantom TM). The positions of the tip of the thumb and the tip of
the index finger in space were indicated by two stereoscopically presented digit
markers (in the form of two small spheres). To start a trial, the participants
had to bring these digit markers within a starting area that was specified by a
large sphere. The starting area was about 20 cm to the right of the dumbbells.
If the digits were in the correct position, the large sphere disappeared. The
participants’ task was to press the spheres of the target dumbbells
together. Figure 1C indicates the relative
size and position of three (invisible) haptic objects. The objects were all
2.5-cm high. If participants touched these, or the surface on which the
dumbbells were lying, the phantoms provided resistance to make the dumbbells and
the surface appear physically present. To press the spheres together,
participants had to move their digits through “force field” objects
(exerting a constant outward force of 0.8
N) until they collided with a simulated
solid object that represented the maximally shortened version of the dumbbells.
We created small gaps between the force fields and the simulated solid object,
so that the participants did not experience a force pushing their fingers back
after having succeeded. A successful grasp was indicated by the appearance of a
pair of maximally shortened dumbbells.
Before starting with the experimental trials of each
block (increasing, decreasing, and static), participants first practiced 10
trials in which the dumbbells remained visible all the time. After that they
practiced for an additional 10 to 20 trials in which they were only allowed to
start moving their hand after the dumbbells had disappeared, as in the actual
experiment. If participants started moving away from the starting position
before the dumbbells had disappeared, they received a warning that they started
too early and the trial was repeated later. If the participants did not succeed
within 3 s of the dumbbells’ vanishing, they were warned that they were
too slow and the trial was repeated later. For each block, there were (2 target
size × 40 repetitions =) 80 experimental trials. This results in a total of
(80 × 3 motion types =) 240 grasping trials for every
participant.
Fourteen right-handed participants performed the tasks
with the dumbbells. Fourteen new right-handed participants performed the tasks
with the spheres. One participant of the latter group was excluded from analysis
as he had profound difficulties with grasping in the virtual setup. In each
group, seven participants did the perceptual task first and seven the grasping.
They were paid for their
participation.
To estimate the remembered distance between the spheres
in the perceptual task, we determined the “remembered size.” This
was the weighted mean for every participant for each of the six conditions
(three motion types and two target sizes). To compute the weighted mean, we
summed the products of the proportion “equal” responses and the
distance between the spheres of the comparison dumbbells, and subsequently
divided this by the total proportion of “equal” responses in that
particular condition. We performed a repeated measures ANOVA on these remembered
sizes with motion type and target size as within-subject factors and task order
(whether the perceptual task was performed first or the grasping) as a
between-subject factor. Representational momentum would be indicated by a larger
remembered size for increasing than for decreasing distance between the
spheres.
For each participant, we computed the representational
momentum effect by subtracting the remembered size for the decreasing condition
from the remembered size for the increasing
condition.
For each grasping trial, we calculated the maximum grip
aperture (i.e., the maximum distance between thumb and index finger during the
reach to grasp movement). Maximum grip aperture scales linearly with object size
(Jeannerod, 1981, 1984). We used a repeated measures ANOVA
with motion type and target size as within-subject factors and order as a
between-subject factor to test for significant effects. Representational
momentum would be indicated by a larger maximum grip aperture for dumbbells that
had been increasing than for dumbbells that had been decreasing.
Similar to the perceptual task, we computed the
representational momentum effect by subtracting the maximum grip aperture for
the decreasing from that for the increasing condition for each
participant.
We took 0.05 as the level of significance. All effects
with a p
< .10 will be mentioned. Mean values
of the dependent variables will be presented as ±
SEM.
Figure 3 plots the
remembered size as a function of motion type and target size for the dumbbells
(A) and the spheres (B).
Figure 3. Perceptual task - the remembered sizes
for each target size and motion type. Error bars represent the
SEM (partly covered by the symbols). A.
Results for the dumbbells. B. Results for the spheres. C. Representational
momentum (remembered size for the increasing condition minus that for the
decreasing condition) for dumbbells and spheres.
Consistent with representational momentum, the
remembered size was larger when the stimuli had been increasing than when they
had been decreasing for both the dumbbells and the spheres. This is reflected by
significant effects of motion type on the remembered size for both kind of
stimuli (repeated measures ANOVAs, dumbbells:
F(2,24)
= 8.81, spheres:
F(2,22)
= 18.37, both
p
< .01). As predicted and
depicted in Figure 3C, representational
momentum was stronger for the spheres than the dumbbells (one-tailed,
independent samples t
test ,
t(25)
= 1.82,
p
= .04). Participants remembered
the distance between the spheres on average as 2.43 ± 0.57 mm larger when
they had been increasing than when they had been decreasing. This was 1.26
± 0.32 mm for the
dumbbells.
As indicated by Figure
3A and 3B, there was a clear effect of target size on the remembered size
(repeated measures ANOVAs, dumbbells:
F(1,12)
= 2120.43, spheres:
F(1,11)
= 9732.41, both
p
< .01). For the dumbbells,
participants remembered the target size of 47 mm on average as being 10.21
± 0.23 mm larger than the target size of 37 mm. This corresponds to a slope
of 1.021 ± 0.023 for the linear fit, which relates remembered size to
object size. For the spheres, the slope was 1.020 ± 0.010.
The repeated measures ANOVA that was performed on the
remembered sizes of the dumbbells did not reveal any other significant effects.
For the spheres, there was a significant interaction between motion type and
size
( F(2,22)
= 10.71,
p
< .01). The nature of the
interaction can be seen in Figure 3B; the
slope is somewhat steeper for the static condition than for the decreasing and
increasing conditions. Another significant interaction for the spheres was
between motion type and order
( F(2,22)
= 5.65,
p = .01). There seemed to be a stronger
representational momentum effect for participants who did the grasping task
first than for participants who did the perceptual task first. In our previous
work using pliers (Brouwer et al., 2003a, 2003b), there was also an
interaction effect between motion type and order on the remembered size, but
this went in exactly the opposite direction; participants who did the perceptual
task first showed representational momentum, whereas the others did not.
Most data points in Figure 3A and 3B are below the line that
indicates veridical performance. This means that participants tended to remember
the stimuli as smaller than they actually were, which is consistent with
previous findings (Brouwer et al.,
2003a, 2003b;
Hayes & Freyd, 2002; Hubbard, 1996; Franz et al., 2001). On average, dumbbells were
remembered as 1.64 ± 0.16 mm too small. For the spheres, this was 0.79
± 0.29 mm. One-tailed one sample t
tests indicated that both biases were significantly different from zero
( t(13)
= 10.37,
p
< .01 and
t(12)
= 2.69, p
= .01, respectively). An
independent samples t test indicated
that the bias was significantly stronger for the dumbbells than for the spheres
(t(25)
= 2.60,
p
= .02).
On average, the remembered sizes of the static
condition are in between those of the increase and decrease condition. Paired
t tests indicated that the remembered
size for the static condition was not different from the remembered size
averaged across the decrease and increase condition (dumbbells:
t(13)
= 1.15,
p
= .27 and
spheres:
t(12)
= 0.77,
p
=
.46).
For the dumbbells, the average maximum grip aperture
was 95 ± 4.64 mm. The participants’ averages ranged between 69 mm and
118 mm. For the spheres, this was 85 ± 4.65 mm with a range of 67 mm until
124 mm.
Figure 4 plots the
maximum grip aperture as a function of motion type and target size for the
dumbbells (A) and the spheres
(B). Figure 4.
Grasping - the maximum grip aperture for each target size and motion type. Error
bars represent the SEM. A. Results for
the dumbbells. B. Results for the spheres. C. Representational momentum (maximum
grip aperture for the increasing condition minus that for the decreasing
condition) for dumbbells and spheres.
There was a significant effect of motion type on the
maximum grip aperture for the dumbbells (repeated measures ANOVA,
F(2,24)
= 4.12,
p
= .03) but not for the spheres
(repeated measures ANOVA,
F(2,22)
= 0.04,
p
= .96). As indicated in Figure 4C, participants opened their fingers on
average 5.90 ± 2.32 mm wider when the dumbbells had been increasing than
when it had been decreasing. This is consistent with representational momentum.
For the spheres, the maximum grip aperture was 0.57 ± 1.64 mm smaller in
the increasing than in the decreasing condition, a trend that goes in the
opposite direction of representational momentum. The difference between these
effects was significant (independent samples
t test,
t(25)
= 2.23,
p
= .04).
For both stimulus types, there was a significant effect
of size (repeated measures ANOVAs, dumbbells:
F(1,12)
= 30.86, spheres:
F(1,11)
= 88.62, both
p
< .01). When grasping
dumbbells of 47 mm, participants opened their fingers 4.18 ± 0.76 mm wider
than when the target size was 37 mm. This corresponds to a slope of 0.418 ±
0.076 for the linear fit, which relates maximum grip aperture to object size.
The slope was 0.402 ± 0.042 mm for the spheres. In other grasping studies,
in which physical objects are grasped, these slopes are usually larger (on
average 0.82; Smeets & Brenner 1999). Our small slope may be due to
participants’ uncertainty about the object’s size and distance
because there is less information available about these properties in grasping
with phantoms in a virtual environment, compared to grasping physical objects in
a natural environment. In our previous work using cubes (Franz et al., 2001) and pliers (Brouwer et al., 2003a, 2003b), in which
participants also grasped virtual objects by using the phantoms, the effect of
target size was small as well (slopes of 0.38 and 0.32, respectively). The
difference in slope, together with the finding that some subjects find it
difficult to use the phantoms (see “ Participants”), indicates that one should be
careful to generalize grasping using phantoms to real grasping. Grasping with
phantoms may be more like grasping impoverished stimuli using tools. However,
our present aim is to measure representational momentum with a task that is more
motorlike than visually judging, rather than investigate real grasping.
The repeated measures ANOVAs on maximum grip aperture
did not reveal any other significant effects.
Figure 4A and 4B show that the average maximum grip apertures
of the static conditions are in between those of the increase and decrease
conditions. Paired t tests indicated
that the maximum grip aperture for the static condition was not different from
the maximum grip aperture averaged across the decrease and increase condition
(dumbbells:
t(13)
= 0.53,
p
= .60 and spheres:
t(12)
= 0.07,
p
=
.95). Relation between perception and action
Figure 5 plots, for
each participant, perceptual representational momentum against representational
momentum in grasping for the dumbbells (A) and the spheres (B). A positive value
means that the remembered width, or the maximum grip aperture, is larger in the
increasing than in the decreasing condition (i.e., representational momentum).
Clearly, there is no (positive) correlation in either of the graphs (dumbbells:
R2
< 0.01,
p
> .99;
spheres :
R2
= 0.08,
p
=
.35). Figure 5. Representational momentum in grasping
plotted against representational momentum in perception. A positive value means
that the effect is in the direction of representational momentum. Every dot
represents the data of one participant. A. Results for the dumbbells. B. Results
for the spheres.
The main findings of the present study are that
representational momentum is influenced first by the type of stimulus change,
and second, by the mode of response (perceptual or motor). Furthermore, the way
in which the type of stimulus change affects representational momentum depends
on whether the task was perceptual or motor in nature. More specifically,
representational momentum was stronger for separately translating spheres than
for transforming dumbbells in a visual judgment task. In contrast, there was no
representational momentum for the translating spheres, but there was
representational momentum for the transforming dumbbells in a grasping task. A
final interesting result is that our stimuli were remembered as smaller than
they actually were. We will discuss these results in more detail and speculate
on explanations below.
In several previous studies, coherent stimulus changes
failed to give rise to representational momentum in visual tasks. Typically,
these studies involved manipulations that changed the identity of the stimulus,
rather than the position. Here we compared memory for the final configuration of
a changing display when that change either consisted of simple translation
(spheres) or also involved object transformation (dumbbells). Consistent with
the previous studies, we found that the simple addition of a connecting bar
– altering a display with two translating spheres into a display with a
single, transforming dumbbell – reduced representational momentum.
Although weak, the dumbbells still gave rise to reliable forward shifts. This
result is consistent with Kelly and Freyd ( 1987). One of their stimuli, a
rectangular shape that grew or shrank along only one axis, also produced a weak
but reliable representational momentum. Both their stimulus and our dumbbells
did not only transform, but also contained a strong translation component. Other
stimuli, in which there were no (clearly) translating components (e.g., the
squares changing luminance of Brehaut & Tipper,
1996), showed an effect opposite to
representational momentum.
The question arises as to why there would be a stronger
representational momentum for translating than for transforming stimuli. Several
authors suggest that the mechanism leading to the typically observed forward
shifts or representational momentum might serve to anticipate the future
position of an object (Brouwer, Middelburg, Brenner, & Smeets, 2003; Hubbard, 1998; Kelly & Freyd, 1987; Nagai, Kazai, & Yagi, 2002). Thus, representational momentum might
be particularly salient when dealing with objects that change position over
time.
Another mechanism may try to guard against anticipation
in situations where it would not be appropriate, such as when changes have the
potential to influence the identity of an object. This could lead to backward
shifts in situations involving changes to object identity rather than object
position (e.g., Brehaut & Tipper, 1996).
These two mechanisms could be competing in cases where both transforming and
translating components are present (cf., competing mechanisms proposed by Freyd & Johnson, 1987).
There was clear evidence for representational momentum
with grasping the dumbbell stimuli, as we had expected from previous studies
that showed strong representational momentum in motor tasks
(Franz et al., 2001;
Brouwer et al., 2003a,
2003b;
Kerzel, 2003). Participants
opened their fingers wider when a pair of dumbbells had been growing than when
it had been shrinking, although we asked the participants to grasp the final
pair and provided the appropriate feedback. Also in line with these previous
studies, representational momentum for the dumbbells appeared to be stronger for
the motor task than the perceptual task. In grasping, the amount of extra grip
aperture for grasping increasing dumbbells relative to static dumbbells (half of
the direction effect, about 3 mm), approaches the amount of extra grip aperture
caused by a 1-cm increase in size (the size effect, about 4 mm). The step size
of the inducing growing dumbbells was 1 cm. Thus, the size of the effect
suggests that participants were aiming to grasp a pair of dumbbells that was
almost one step further in the direction of the change. For visual judgment
tasks, representational momentum is usually much smaller than the step size of
the inducing stimuli.
In contrast to the large effect of the direction of
change in grasping dumbbells, there was no effect of direction at all for
grasping the spheres. Note again that the spheres and the dumbbells were
identical in all haptic and visual respects, except the spheres of the dumbbells
were visually connected by a bar.
Because grasping and perception produced opposite
effects of type of stimulus change on representational momentum, we clearly
cannot generalize the hypothesized explanation for the difference between
translating and transforming stimuli from the visual task to the motor task. The
different effect of type of stimulus change on a motor and a visual task shows
that anticipation in grasping and perception are not simply governed by the same
mechanism or by the same visual information. This was already suggested by our
previous study involving opening and closing pliers (Brouwer et al., 2003a, 2003b). In that study,
there was very little evidence of visual representational momentum, but there
was representational momentum in grasping. Furthermore, there was no
between-subject correlation between representational momentum measured with the
perceptual and the grasping task. However, the dissociation found in that study
could have been special for cases in which there was no visual representational
momentum. In the present study, visual representational momentum occurred for
both the perceptual and the grasping task, but a dissociation was still
found.
The separate visual pathways hypothesis (Goodale &
Milner, 1992) proposes that visual
information is processed in two cortical streams. The ventral stream processes
visual information that is used for perceptual identification of objects,
whereas the dorsal stream processes information to serve visually guided action.
According to this theory, a difference between perception and action is not
unexpected. However, the theory further states that the dorsal pathway (i.e.,
action) is largely resistant to illusions, in contrast to the ventral pathway
(perception). Studies that support the visual streams hypothesis show more
accurate performance for grasping the center disc of the Ebbinghaus illusion
(Aglioti, DeSouza, & Goodale, 1995;
Haffenden & Goodale, 1998) than
for visually judging its size, which clearly reflects the illusion. The results
for the spheres were in the direction expected by the visual streams hypothesis.
In contrast, the pattern found by Kerzel ( 2003) and by us with the pliers and the
dumbbells, was exactly the other way around: participants were more accurate in
the visual than in the motor task. We prefer to explain different results for
perception and action by a lack of properly matching the motor task to the
visual task (Pavani et al., 1999; Franz et
al., 2000; Franz, 2001; Franz et al., 2003) and a difference in the use of
information for the different tasks (Smeets, Brenner, de Grave, & Cuijpers,
2002).
In our pliers study, we found a stronger forward shift
for closing than for opening pliers. Similarly, Hayes and Freyd ( 2002), who used growing and shrinking squares
(or approaching and receding squares), found a stronger forward shift for
shrinking than for growing squares. To clarify whether there was a difference in
strength of representational momentum between the different directions of
motion, or whether there was a general tendency to remember things as too small
that, together with effects of direction of motion, determined the final
remembered size, we followed the example of Hubbard ( 1996) and included a static condition in
this study. Consistent with Hubbard’s results, we found that the average
remembered size for the static condition was smaller than the actual target
size, and that the remembered size of the static stimuli was in between that of
the decreasing and increasing stimuli. Thus, the remembered size seems to be
determined by the actual target size, representational momentum, and a general
bias to remember the objects as a certain amount too small. This bias could be
related to boundary extension (Intraub, 1997;
Hubbard, 1996). Boundary extension is
the tendency to remember a scene as if the limits of view have been extended
outward, which would be, in the experiments mentioned, equivalent to remembering
objects as smaller than they were. This tendency was stronger for the dumbbells
than for the spheres. If participants attended more to the whole stimulus in the
case of the dumbbells and to only one sphere when they were separate objects,
this is not a surprising difference. Boundary extension that affects the whole
dumbbell gives rise to dumbbells that are remembered as smaller than they were,
but boundary extension that affects only one sphere gives rise to a sphere that
is remembered as smaller than it was, but not to a (inward) change of position
of the sphere.
In summary, we conclude that visual representational momentum is stronger for objects changing position than for transforming objects. Measuring representational momentum with a motor task gives the opposite result. This opposite effect of object change indicates that different information is used in judging stimuli for a visual task than for a motor task, or that different mechanisms process information for these two types of tasks. A clear goal for future studies will be to try to specify more precisely the nature of these differences. For example, examining eye movement patterns or assessing attentional deployment during grasping and perceptual judgments may help to shed light on the type of information being extracted. Similarly, such measures could also be used to investigate possible strategy differences adopted by observers when faced with the spheres or the dumbbells. Our use of blocked designs may have increased the tendency for observers to adopt specific strategies. Randomly presenting spheres or dumbbells may be a useful way to manipulate the use of strategies or more generally explore the impact of
increased uncertainty (Kerzel, 2002).
Thanks to Andries Hof for collecting data. Thanks to
two anonymous referees for helping improve the manuscript. The first author was
supported by the European Commission (Grant HPRN-CT-2002-00226).
Commercial relationships: none.
Corresponding author: Anne-Marie
Brouwer.
Email:
Anne-marie.brouwer@tuebingen.mpg.de.
Address: Max Planck Institute for Biological
Cybernetics, Tübingen,
Germany.
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