Detection of regularities (e.g., symmetry, repetition) can be used to investigate object and shape perception. Symmetry and nearby lines may both signal that one object is present, so moving lines apart may disrupt symmetry detection, while repetition may signal that multiple objects are present. Participants discriminated symmetrical/irregular and repeated/irregular pairs of lines. For vision, as predicted, increased line separation disrupted symmetry detection more than repetition detection. For haptics, symmetry and repetition detection were similarly disrupted by increased line separation; also, symmetry was easier to detect than repetition for one-handed exploration and for body midline-aligned stimuli, whereas symmetry was harder to detect than repetition with two-handed exploration of stimuli oriented across the body. These effects of exploration and stimulus orientation show the influence of modality-specific processing rather than properties of the external world on regularity detection. These processes may, in turn, provide insights into the nature of objectness in vision and in touch.
Detection of regularities (e.g., symmetry, repetition) can be used to investigate object and shape perception. Symmetry and nearby lines may both signal that one object is present, so moving lines apart may disrupt symmetry detection, while repetition may signal that multiple objects are present. Participants discriminated symmetrical/irregular and repeated/irregular pairs of lines. For vision, as predicted, increased line separation disrupted symmetry detection more than repetition detection. For haptics, symmetry and repetition detection were similarly disrupted by increased line separation; also, symmetry was easier to detect than repetition for one-handed exploration and for body midline-aligned stimuli, whereas symmetry was harder to detect than repetition with two-handed exploration of stimuli oriented across the body. These effects of exploration and stimulus orientation show the influence of modality-specific processing rather than properties of the external world on regularity detection. These processes may, in turn, provide insights into the nature of objectness in vision and in touch.
Regularities provide an important cue to the shape and structure of objects in our
external world. Most research on regularities has focused on bilateral mirror
reflection (henceforth termed symmetry). Symmetry is a property of many objects,
including our own bodies and those of most animals, fruit, plants, and manmade
objects such as tools (for reviews, see Treder, 2010; Tyler,
1995; Wagemans, 1995,
1997). Symmetry aids
perceptual grouping, for example, by acting as a cue for figure-ground segregation
(Machilsen, Pauwels, & Wagemans,
2009). Symmetry is usually easier to detect than other regularities such
as repeated lines which have been translated (henceforth termed repetition) or
rotational symmetry (Julesz,
1971).It has been proposed that the presence of different types of regularity may be used
to signal different properties in the world (Koning & Wagemans, 2009; Treder & van der Helm, 2007; Van der Helm & Treder, 2009). Of particular
relevance for the present paper is whether symmetry may signal the presence of a
single, bilaterally symmetric object, while repetition signals the presence of
multiple, similarly shaped objects. This hypothesis has been supported by a number
of studies which have reported an interaction between objectness and regularity-type
(e.g., Baylis & Driver, 1995;
Bertamini, 2010; Bertamini, Friedenberg, & Kubovy,
1997; Cecchetto & Lawson,
2016). The precise nature of this interaction varies across different
studies (Koning & Wagemans,
2009) but, in general, symmetry is easier to detect for one-object
stimuli with two regular sides than for two-objects stimuli where the facing sides
of the two objects are regular. In contrast, repetition was easier to detect for
two-objects stimuli than one-object stimuli.Koning and Wagemans (2009)
suggested that this interaction between objectness and regularity-type might reflect
the basic strategies which vision uses to extract information, rather than
high-level, cognitive strategies such as mental translations. To test their account,
they again used pairs of edges belonging to either a single object or two objects.
However, unlike previous studies which used 2D shapes their stimuli appeared to be
planar, 3D objects tilted in depth by 45°. The use of these projected 3D
objects to test regularity detection minimized figure-ground ambiguity and prevented
the use of matching strategies involving simple mental translations. Despite these
changes, Koning and Wagemans
(2009) found an interaction between objectness and regularity-type,
replicating previous results. They therefore concluded that structural differences
between stimuli, and not the use of high-level matching strategies, underlay the
one-object advantage for symmetry and the two-objects advantage for repetition.However, all of the studies reviewed above tested vision only. Recently, Cecchetto and Lawson (2016) tested
whether Koning and Wagemans’
(2009) conclusion generalized to regularity detection in a different
modality, namely haptics (our sense of active touch). Haptics is the only other
modality which is specialized at extracting shape information and there are many
similarities in how vision and haptics identify objects. Across a number of studies,
we have compared the ability of vision and haptics to do the same tasks using the
same stimuli in order to examine whether effects found for visual processing
generalize to haptics (e.g., Collier &
Lawson, 2016; Craddock &
Lawson, 2009a, 2009b;
Lawson, 2009; Martinovic, Lawson, & Craddock,
2012). In the present study, we extended our approach to test regularity
detection for symmetry and repetition. It is well established that haptics can
detect symmetry (see Cattaneo et al.,
2014, for a recent review) but, as far as we are aware, no other studies
have investigated the haptic detection of repetition.Cecchetto and Lawson (2016) found
that there was an important difference between visual and haptic regularity
detection. For vision, we found a one-object advantage for detecting symmetry and a
two-objects advantage for detecting repetition, replicating the interaction reported
by Koning and Wagemans (2009) and
others. However, for haptics, there was a one-object advantage for both symmetry and
repetition detection. These results suggest that effects on regularity detection may
not be informing us about properties of the external world. Instead they may be
telling us about differences in processing across our sensory systems. This
alternative account was examined in the present study. However, in the present
studies, unlike most previous studies including Cecchetto and Lawson (2016), we did not use planar,
closed-contour shapes. As we now explain, this was due to a concern raised by Van der Helm and Treder (2009).Van der Helm and Treder (2009)
noted that most previous studies investigating the role of objectness on regularity
detection tested anti-repetition rather than true repetition, see Figure 1. True regularities occur
if two contours have the same polarities whereas anti-regularities occur if they
have opposite polarities, for example with respect to curvature (so mismatched
concavities and convexities), color, or luminance. Van der Helm and Treder’s (2009) findings indicated that
the visual system treats anti-regularities differently to regularities. All of the
studies discussed so far tested anti-repetition (Baylis & Driver, 1995; Bertamini, 2010; Bertamini et al., 1997; Koning & Wagemans, 2009; Cecchetto & Lawson, 2016). Van der Helm and Treder therefore argued
that none of these studies actually tested whether repetition detection was easier
for two-objects compared to one-object stimuli. They did, though, note that both
Corballis and Roldan (1974) and
Treder and van der Helm
(2007) investigated this issue.
Figure 1
An illustration of four types of regular, two-objects, planar shapes
varying in regularity-type (symmetry vs. repetition) and regularity-polarity
(truly regular vs. anti-regular) based on Figure 1 of Van der Helm and Treder (2009). For
anti-repetition and anti-symmetry stimuli, the two task-critical, regular
contours have opposite polarities in terms of convexity (+) and concavity
(−), defined with respect to the closed-contour object, and in terms
of color and the luminance of the object, defined relative to its
background. Baylis and Driver
(1995), Bertamini
(2010), Bertamini et
al. (1997), Koning
and Wagemans (2009), and Cecchetto and Lawson (2016) all used two-objects stimuli
with the task-critical contours on facing sides of the two objects. This
meant that these task-critical contours had true symmetry (the inner two
lines in the top left case here) but anti-repetition (the inner two lines in
the bottom right case here).
Corballis and Roldan (1974) asked
people to compare dots in two 3 × 2 arrays. The two arrays were
either adjacent (so they could be perceived as a single whole) or separated by a gap
(so they may have appeared as two, separate objects). The dot patterns were either
symmetrical or repeated so all the stimuli were regular and, unusually, the task was
to discriminate symmetry from repetition. Symmetry was detected faster for adjacent
compared to separated arrays, though this difference was not tested statistically.
There was also a trend in the opposite direction for repetition detection (though it
was probably not significant), so for an advantage for the separated arrays.Treder and van der Helm (2007)
used stereoscopic depth to assign the two halves of symmetrical and repeated dot
patterns to either the same or to two different depth planes. They took advantage of
the fact that location in depth influences the grouping of parts with nearby parts
being more likely to be perceived as belonging to the same object. Splitting the
stimuli across different depth planes disrupted symmetry detection but had little
effect on repetition detection, so only symmetry processing clearly benefitted from
structural correspondences occurring within a depth plane.To summarize, Van der Helm and Treder
(2009) argued that only two studies have investigated the interaction
between regularity-type and objectness: Corballis and Roldan (1974) and Treder and van der Helm (2007). However, in both of these
studies the interaction (symmetry detection being easier for one-object compared to
two-objects stimuli, and vice versa for repetition detection) was found only for dot
stimuli, and in neither study was there a clear two-objects advantage for
repetition. In addition, Corballis and
Roldan (1974) tested regularity discrimination rather than regularity
detection, and they did not statistically test whether there was a one-object
advantage for symmetry, or whether there was a two-objects advantage for repetition.
Thus, there is still a dearth of evidence as to whether true repetition (as opposed
to anti-repetition) is easier to detect visually for two-objects stimuli relative to
one-object stimuli and this has never been tested for haptics.This issue is of wider importance because it may provide insights into what defines
an object in vision and touch. The concept of objectness is central to many aspects
of spatial and conceptual organization in both perception and cognition. However, it
has proven difficult to define what constitutes an object (Feldman, 2003). Researchers claiming to manipulate
objectness often make little attempt to justify their choice of stimuli. The present
study aims to introduce an approach which allows us to identify and to compare
potential cues to objectness in both vision and touch. We do not assume that
objectness is an all-or-nothing property of a stimulus and we think that multiple
cues combine to determine whether a given stimulus is perceived as an object. We are
not aware of any previous research that has tried to define what it means to be a
haptic object. Our approach is therefore preliminary and we will not claim to
provide conclusive evidence about the nature of objectness in haptics. Nevertheless,
this topic is an important one which has been neglected for too long, and we think
that progress can be made in trying to understand objectness across different
modalities.The present study tested a novel prediction based on previous research suggesting
that symmetry detection is easier for one-object stimuli while repetition detection
is easier for two-objects stimuli. We hypothesized that, on average, closer lines
are more likely to be perceived as belonging to the same object and more distant
lines as belonging to two different objects (see also Corballis & Roldan, 1974; Treder & van der Helm, 2007). This hypothesis
leads to the prediction that it should be easier to detect symmetry when lines are
closer because both cues (line separation and the type of regularity) indicate that
one object is present. Conversely, repetition should be harder to detect when lines
are closer because one cue (line separation) indicates that one object is present
whereas the other cue (the type of regularity occurring – here, repetition)
indicates that multiple objects are present. We investigated these predictions by
testing whether effects of the type of regularity being detected (symmetry vs.
repetition) interacted with line separation. This approach is conceptually similar
to that taken by Treder and van der Helm
(2007). They varied regularity-type (symmetry vs. repetition) and
stereoscopic depth (the two stimulus halves were on the same vs. on different depth
planes) to investigate how regularity detection was influenced by whether these cues
provided consistent or conflicting interpretations of objectness. To avoid the
issues discussed above arising from using anti-regularities (see Van der Helm & Treder, 2009),
and to simplify the stimuli, the experiments reported here presented only lines
rather than planar shapes (see Figure
2).
Figure 2
The upper box illustrates the type of planar, 2D stimuli that have
previously been used to test the interaction between regularity-type
(symmetry vs. repetition) and objectness (one vs. two). The pairs of
task-critical, regular lines are highlighted here but they were not shown to
participants. Baylis and Driver
(1995), Bertamini
(2010), Bertamini et
al. (1997), Koning
and Wagemans (2009), and Cecchetto and Lawson (2016) presented stimuli like those
in the top two rows of the upper box (so true symmetry and anti-repetition
stimuli); they did not show any true repetition or anti-symmetry stimuli.
The lower box illustrates the line-only stimuli used in the present studies.
Note that the task-critical, symmetrical, and repeated lines for all four
rows of planar stimuli shown in the upper box are identical to these lines.
Regularity polarity (true versus anti) cannot be defined unambiguously for
the line stimuli since this would require labelling one side of the line as
“inside”.
In summary, in the three studies reported here we contrasted how potential cues to
objectness, such as the spatial separation between two lines, influenced the
detection of symmetry and repetition. As in Cecchetto and Lawson (2016), we used matched stimuli and tasks
to compare regularity detection for vision (Experiment 1) and for haptics
(Experiments 2 and 3). The goal of this research was to investigate whether there is
a one-object advantage (cued by a small line separation) for symmetry detection and
a two-objects advantage (cued by a large line separation) for detecting true
repetition, and whether any such effects found for regularity detection reflect
modality-specific processing, or if they reveal differences arising directly from
the presence of regularities out in the physical world.
Experiment 1
In Experiment 1 participants saw pairs of vertically aligned, 2D lines. We
investigated whether people found it harder to visually detect regularities (either
symmetry or repetition, in separate blocks) when the horizontal separation between
the two lines increased from 25 mm up to 50 mm and to 100 mm.
We expected that smaller separations would make it more likely that the lines were
perceived as belonging to a single object, whereas larger separations were more
likely to be perceived as belonging to two different objects. We also hypothesized
that symmetry is used as a cue for the presence of a single object, whereas
repetition provides evidence for the presence of multiple objects. We therefore
predicted that symmetry detection should be easier for small relative to large line
separations. Here, nearby pairs of symmetrical lines provide consistent cues that a
single object is present whereas distant pairs of symmetrical lines provide
conflicting cues about objectness. The opposite pattern was predicted for
repetition. Here, well-separated pairs of repeated lines provide consistent evidence
for the presence of two objects, while nearby, repeated lines provide conflicting
cues about objectness. However, there are independent reasons why regularity
detection may be harder at large line separations, such as the difficulty of
visually perceiving more peripheral stimuli. Any such effects would counter the
expected large-separation advantage for repetition (while enhancing the predicted
large-separation cost for symmetry). We therefore simply predicted that increasing
line separation would disrupt symmetry detection more than repetition detection.
Method
Participants
Twenty-four students from the University of Liverpool (16 females, mean
age = 20 years,
SD = 2.8, range 18–31) volunteered to
take part in the experiment. In all of the experiments reported in this
paper the participants had normal or corrected-to-normal vision, they
self-reported as right-handed, they had no known conditions affecting their
sense of touch, and most received course credits in exchange for their time.
All the experiments received ethical approval from the local Ethics
Committee.
Materials
We produced a set of 480 pairs of lines based on the 40 unique lines used in
Experiment 1 of Cecchetto and
Lawson (2016). However, the vertices of these unique lines were
rounded to ensure that when the lines were felt (in Experiments 2 and 3)
there would be no sharp corners which might be difficult to explore by
touch. Each unique line had four vertices with the top and bottom of each
line vertically aligned, see Figure 3. Each unique line was paired with a mirror-reflected
version of itself, with the same version of itself, with a mirror-reflected
version of a different unique line and, finally, with a repeated version of
a different unique line. This produced the symmetrical, repeated, and two
irregular stimuli, respectively. For the irregular stimuli, unique line 17
could be paired with unique line 3 for its two irregular stimuli, while
unique line 3 could be paired with unique line 8, and so on. There were 480
trials in total (40 unique lines × Regular/irregular
stimuli × Symmetry/repetition
regularity-type × Small/medium/large line
separations).
Figure 3
The 20 unique lines used to generate the regular stimuli for
Experiments 1, 2, and 3. In Experiment 1 only, 20 additional unique
lines were used which were produced in a similar way. The unique
lines are shown here ordered from easiest (top left) to hardest
(bottom right) in terms of accuracy in previous regularity detection
tasks (discriminating symmetrical from irregular stimuli and
repeated from irregular stimuli in Experiment 1 of Cecchetto & Lawson,
2016).
Pairs of lines were presented as 2D images on a computer monitor and were
viewed from a distance of approximately 50 cm. The LCD widescreen
monitor (Dell Inc., USA) was 58 cm diagonally and had a resolution of
1280 × 1024 pixels. Each line was 3 mm wide and
100 mm high. The top and bottom of each line was positioned
12.5 mm each side of the midpoint of the monitor for the 25 mm
separated lines, 25 mm each side of it for the 50 mm separated
lines, and 50 mm each side of it for the 100 mm separated
lines. The 100 mm separated lines subtended around
11° × 11°.
Design
All participants did one block of symmetry detection and one block of
repetition detection, with block order counterbalanced across participants.
Each block had 240 trials (40 unique
lines × Regular/irregular
stimuli × Small/medium/large line separations). These
trials were presented in a different, random order for each participant.
Procedure
Participants sat in a normally lit room. Participants were instructed to
center their body midline to the center of the computer monitor. Before
starting each block, participants were told about the nature of the
regularity they were about to detect, its orientation, and that the stimuli
could have different line separations. Each block of experimental trials was
preceded by 10 practice trials taken from that block. These practice trials
were the same for all participants and they included five regular and five
irregular trials and a mix of the three line separations. At the start of
each trial, a central fixation cross appeared on the monitor for 1 s.
This was replaced by the stimulus which remained on the monitor until the
participant responded. Visual prompts about how to respond were presented on
the monitor whenever the stimulus was visible, see Figure 4. Participants responded using the
computer keyboard, pressing “s” for regular trials and
“k” for irregular trials as quickly and as accurately as
possible. Reaction times (RT) were recorded from stimulus onset until the
participant responded. The experiment took around 30 min to
complete.
Figure 4
An example of a large line separation, symmetrical stimulus
presented visually on the computer monitor in Experiment 1.
Results
Correct RT faster than 0.4 s or slower than 3.5 s were removed as
outliers (less than 2% of trials). To be consistent with reporting in previous
studies, ANOVAs were conducted on the mean correct RT and on the percentage of
errors for regular trials only (also performance on irregular trials is
difficult to interpret theoretically). In all three experiments reported here,
we also analyzed measures of sensitivity (d′) and bias (c′) which
included data from irregular trials, see Appendix. There were two
within-participants factors in the ANOVAs: regularity-type (symmetry or
repetition) and line separation (small, medium, or large).Regularity-type was significant for RT,
F(1, 23) = 19.71,
p < .001,
ηp2 = .46, but not for errors,
F(1, 23) = 0.01,
p = .9,
ηp2 = .00. Symmetry detection
(0.93 s, 6% errors) was faster but not more accurate than repetition
detection (1.09 s, 6%).Line separation was significant for both RT,
F(2, 46) = 135.04,
p < .001,
ηp2 = .85, and errors,
F(2, 46) = 29.19,
p < .001,
ηp2 = .56. Post hoc Newman-Keuls
analyses (p < .05) revealed that regularity
detection was both faster and more accurate with small separations
(0.89 s, 3% errors) than with medium separations (1.01 s, 6%) and,
in turn, that detection was both faster and more accurate with medium
separations compared to large separations (1.13 s, 9%).Finally, the interaction of Regularity-type × Line
separation was significant for both RT,
F(2, 46) = 12.32,
p < .001,
ηp2 = .35, and errors,
F(2, 46) = 11.59,
p < .001,
ηp2 = .34, see Figure 5. To understand this interaction, we
calculated the difference between regularity detection for the largest
(100 mm) compared to the smallest (25 mm) line separation and
conducted an ANOVA on these differences. This revealed that increased line
separation (100 mm–25 mm) was significantly more disruptive
for detecting symmetry (0.28 s, 10% errors) than for detecting repetition
(0.19 s, 2%) for both RT,
F(1, 23) = 6.74,
p = .016,
ηp2 = .28, and errors,
F(1, 23) = 12.62,
p = .002,
ηp2 = .35.
Figure 5
Results for regular trials for Experiment 1 for the visual detection
of symmetry (Sym) and repetition (Rep) for line separations of
25 mm, 50 mm, and 100 mm for RT (A) and errors (B).
Error bars represent one standard error of the mean. In this, and the
remaining figures showing experimental results, the icons at the base of
each bar schematically represent the type of stimuli in that condition:
symmetrical or repeated with small, medium, or large separations between
each pair of lines.
Discussion
In Experiment 1, our hypothesis was that line separation and regularity-type are
both factors which provide evidence about objectness. We therefore predicted
that effects of line separation should interact with those of regularity-type,
with the disruptive effect of increased line separation being greater for
symmetry detection than for repetition detection. Our results for visual
regularity detection confirmed this prediction. Converging evidence for this
interaction between the effects of objectness and regularity-type on vision has
been reported when objectness is manipulated using planar shapes like those
shown in Figure 1 (Baylis & Driver, 1995; Bertamini, 2010; Bertamini et al., 1997; Koning & Wagemans, 2009;
Cecchetto & Lawson,
2016). Further discussion of these results for vision is deferred
until we have described the Results of Experiments 2 and 3, which investigated
the interaction between regularity-type and line separation for haptic
regularity detection.
Experiment 2
Experiment 2 largely replicated Experiment 1, except that the stimuli were presented
haptically, as 3D raised lines, rather than visually, as 2D digital images. We again
investigated the effects of type of regularity (symmetry or repetition) and line
separation on regularity detection. Based on the results of Experiment 1, we might
expect that symmetry should be easier to detect with small line separations, since
nearby lines and symmetry may provide consistent evidence that a single object is
present, whereas large line separations and symmetry provide conflicting cues about
objectness. The opposite pattern might be expected for repetition, with repetition
being easier to detect at large line separations, since repetition and distant lines
may provide consistent cues that two objects are present. Note, though, that there
are independent reasons why regularities might become harder to detect at large line
separations (irrespective of whether symmetry or repetition is being detected). For
example, participants probably find it harder to align their fingers precisely in
space when they are further apart. From debriefing and informal observation, we
believe that finger alignment is critical for haptic regularity detection. Any such
independent effects would counter the expected advantage for large line separations
for repetition (while enhancing the cost for large line separations for symmetry).
We therefore simply predicted that, if haptic regularity detection behaves like
visual regularity detection, then increased line separation should disrupt symmetry
detection more than repetition detection.However, importantly, when we manipulated perceived objectness in previous
experiments using closed-contour, planar stimuli rather than line separation (Cecchetto & Lawson, 2016; see
Figure 2), we obtained an
interaction between objectness and regularity-type for vision but not for haptics.
Based on these findings, if haptics again behaves differently to vision, in
Experiment 2 compared to Experiment 1, we would not predict a greater influence of
line separation when haptically detecting symmetry compared to repetition.The same 24 participants from Experiment 1 took part in Experiment 2, in a
second, separate session. This haptic session was always conducted before
visual testing occurred in Experiment 1 (on average, 6 days earlier,
range 0–15 days). However, for ease of explanation, we
described the visual experiment first.There were 240 stimuli, comprising half of the 480 pairs of lines used in
Experiment 1. The pairs of lines were based on 20 of the 40 unique lines
used in Experiment 1. These 20 lines were selected to span the range of
difficulty that we observed in Experiment 1 of Cecchetto and Lawson (2016), which used the
same lines, see Figure 3.
This was done by ordering performance for regularity detection for each line
from best to worst and then selecting alternate lines.We used a laser cutter to produce the 3 mm
wide × 100 mm tall plastic lines from
5 mm thick acrylic sheets. Pairs of lines were glued onto
15 cm wide × 10 cm tall cardboard bases
with the top and bottom of each line aligned with the top and bottom of the
base, respectively, so the long axes of each line lay parallel to each
other. The dimensions of the stimuli were matched to the dimensions of the
stimuli used in Experiment 1 so the top and bottom of each line was
positioned 12.5 mm each side of the midpoint of the base for the
25 mm separated lines, 25 mm each side of it for the
50 mm separated lines, and 50 mm each side of it for the
100 mm separated lines.
Line Separation Discrimination Check
We conducted a rating study to check that participants in Experiment 2 could
haptically discriminate between the line separations presented. Twenty-four
students from the University of Liverpool (17 females, mean
age = 19 years, SD = 1.5,
range 18–25) volunteered to take part. Twelve participants were allocated
to the two-handed exploration group. They felt two lines simultaneously with
their two index fingers. The remaining 12 participants were allocated to the
one-handed exploration group. They used their right index finger to feel the
right line and their right thumb to feel the left line. This rating study used
the same procedure and a subset of the trials used in Experiment 2. Each
participant completed the same nine trials which were presented in a fixed,
pseudorandom order. These comprised three symmetry trials, three repetition
trials, and three irregular trials, each with a small, medium, and large line
separation. Participants responded verbally as to, first, whether each pair of
lines was symmetrical, repeated, or irregular, and then whether each pair of
lines was separated by a small, medium, or large gap. Thus, both tasks involved
distinguishing between three categories. Accuracy was similar for the regularity
discrimination task (21% errors with one hand, 27% with two hands) and the line
separation discrimination task (23% errors with one hand, 21% with two
hands).This was identical to Experiment 1 except for the following points.
Participants did the same block order (symmetry detection then repetition
detection or vice versa) as they had done in Experiment 1. However, because
regularity detection is much faster for vision than for haptics, and because
there were only half the stimuli in Experiment 2 as in Experiment 1,
participants only did a quarter of the number of trials in Experiment 2 as
in Experiment 1. Participants thus completed 120 of the possible 240
experimental trials in 2 blocks of 60 trials. The 240 trials (20 unique
lines × Regular/irregular
stimuli × Small/medium/large line separations) were
divided into 4 blocks of 60 trials. Each of these blocks included 20 stimuli
at each of the three line separations and they also all included three
stimuli based on each of the 20 unique lines with half the stimuli being
regular and half irregular in each block. Trials within a block were
presented in a fixed, pseudorandom order. The assignment of participants to
blocks was counterbalanced by dividing the participants into six subgroups
of four participants and then, within each subgroup, all four blocks were
completed once as the first block and once as the second block.This was identical to Experiment 1 except for the following points. Stimuli
were presented in front of participants on a 70 cm high table, see
Figure 6. A curtain
hung directly in front of the participant, around 15 cm inside the
edge of the table. Participants put their hands under the curtain, hiding
both the stimuli and their hands from view. On the table in front of the
curtain there were two labels, “same” on the left and
“different” on the right, to remind participants which foot
pedal they should use to respond on regular and irregular trials
respectively. Participants were instructed to center their body midline with
the midpoint of the two response labels and the midpoint of the two foot
pedals.
Figure 6
Haptic exploration of a large line separation (100 mm),
symmetrical stimulus in Experiment 2 as seen from the
experimenter’s perspective. Note the startpoint patch at the
top of the stimulus.
The experimenter placed stimuli, one at a time, in a recess (15 cm
wide × 10 cm tall) within a 45 cm
wide × 30 cm tall foamboard frame. The frame
ensured that the stimuli were presented at a fixed position and orientation.
The center of the recess was in line with the participant’s body
midline and was 25 cm from the edge of the table and approximately
40 cm from the participant. There was a soft patch on the frame,
positioned above the middle of the top of the recess, see Figure 6. Participants
rested both of their index fingers on this startpoint patch before beginning
each trial, so they started exploring lines from the top.Before starting the experiment, participants were shown visually four
practice stimuli. These stimuli were similar to the experimental stimuli:
two were regular, two were irregular, and all had a medium separation.
Participants then did four practice trials haptically using these stimuli.
They were instructed to feel one line with each of their two index fingers,
and to decide whether the lines were regular.At the start of each trial the experimenter placed a stimulus in the recess,
then triggered an audible “go now” signal using the computer.
This indicated to the participant that they should move their fingers from
the resting position on the startpoint patch, to begin to explore the two
lines. Participants were told to respond as quickly and as accurately as
possible by pressing a foot pedal. Reaction times (RT) were measured from
the offset of the go signal to the participant’s pedal response.
Following their response, a high or a low pitch feedback sound was emitted
to indicate a correct or a wrong answer respectively.After the first block of 60 experimental trials, participants were instructed
about the new regularity that they would have to detect. They were again
shown visually four new practice stimuli which were then used in four haptic
practice trials before they did the second block of 60 experimental trials.
The experiment took around one hour to complete. Afterwards the experimenter
checked to ensure that the participant had not seen any of the stimuli.No participant was replaced. Correct RT faster than 1 s or slower than
35 s were removed as outliers (less than 1% of trials).2 As in
Experiment 1, ANOVAs were conducted on the mean correct RT and on the percentage
of errors for regular trials only. Analyses of measures of sensitivity
(d′) and bias (c′) are given in the Appendix. There were two
within-participants factors in the ANOVAs: regularity-type (symmetry or
repetition) and line separation (small, medium, or large).Regularity-type was significant for both RT,
F(1, 23) = 6.86,
p = .015,
ηp2 = .23, and errors,
F(1, 23) = 11.77,
p = .002,
ηp2 = .34. Symmetry detection
(7.2 s, 8% errors) was both faster and more accurate than repetition
detection (8.7 s, 16%).Line separation was significant for RT,
F(2, 46) = 3.80,
p = .03,
ηp2 = .14, and was marginally
significant for errors, F(2, 46) = 2.97,
p = .06,
ηp2 = .11. The overall pattern was
for regularity to be easiest to detect at small separations (7.6 s, 9%
errors), in between for medium separations (8.0 s, 12.5%), and hardest
for large separations (8.2 s, 15%). However, in post hoc Newman-Keuls
analyses only the difference in speed between small and large separations was
significant (p < .05).Finally, the interaction of Regularity-type × Line
separation was not significant for RT,
F(2, 46) = 0.50,
p = .6,
ηp2 = .02, or for errors,
F(2, 46) = 0.70,
p = .5,
ηp2 = .03. The effect of line
separation was similar for symmetry detection and repetition detection, see
Figure 7.
Figure 7
Results for regular trials for Experiment 2 for the haptic detection
of symmetry (Sym) and repetition (Rep) for line separations of
25 mm, 50 mm, and 100 mm for RT (A) and errors (B).
Error bars represent one standard error of the mean.
Experiment 2 revealed a modest cost of increasing line separation on haptic
regularity detection together with an overall advantage for detecting symmetry
compared to repetition. Unlike visual regularity detection in Experiment 1, we
did not find a greater cost of line separation when detecting symmetry compared
to repetition, for either the RT or the error analyses of regular trials. This
difference between the results of Experiments 1 and 2 suggests that
modality-specific processing influences the detection of regularities. This
conclusion is consistent with the findings of Cecchetto and Lawson (2016) where we compared regularity
detection in vision and touch for planar, closed-contour shapes (see Figure 2). However, we should
note that the results of the sensitivity analysis revealed an interaction in the
predicted direction between the effects of line separation and regularity-type,
see the Appendix, so there was some inconsistency in the results. Experiment 3
was therefore conducted to investigate this issue further.
Experiment 3
Experiment 3 was conducted to probe whether effects on regularity detection reflect
perceptual processes unique to haptics rather than reflecting properties of the
physical stimuli. This question was addressed by, first, changing the orientation of
the lines relative to a body-centered spatial frame of reference and, second,
altering the manner of haptic exploration. Both of these manipulations were expected
to change modality-specific aspects of perceptual processing while leaving unaltered
the stimuli and their surrounding environment. If an understanding of regularity
detection tells us about the information available to us in the world then neither
manipulation should affect performance. However, if regularity detection is
sensitive to how information is acquired and processed then both manipulations may
influence performance. The results for separate pairs of lines in Experiments 1 and
2 here, and for planar, closed-contour shapes in Cecchetto and Lawson (2016), suggest that effects of
regularity-type and objectness differ for visual versus haptic regularity detection.
This supports the latter prediction.Experiment 3 replicated Experiment 2 except for two main points. First, the stimuli
were rotated by 90° so that the axis of regularity ran perpendicular to the
body midline (in the across condition) rather than being aligned with it (as in
Experiments 1 and 2). When stimuli are aligned with their body midline, participants
can represent symmetrical stimuli using a highly salient spatial frame of reference
based on the symmetry of their own body (e.g., Ballesteros, Millar, & Reales, 1998). Having the axis of
regularity of symmetrical stimuli aligned with the axis of bilateral symmetry of the
participant’s own body midline may thus aid symmetry detection relative to
repetition detection. However, any benefit from using this salient reference frame
should be weaker, or absent, if the axis of regularity of symmetrical stimuli is
perpendicular to the axis of bilateral symmetry of the participant’s own body
midline, as it was for across stimuli in Experiment 3. We therefore predicted that
symmetry detection would be harder in the across condition in Experiment 3 than in
the aligned condition in Experiment 2.Second, in Experiment 3 the manner of stimulus exploration was manipulated between
participants. One group used the same, two-handed exploration tested in Experiment
2, with their two index fingers each feeling one of the two lines, see Figure 8. A second group explored
stimuli using only one hand. They used their right index finger to explore the top
line and their right thumb to explore the bottom line. We reasoned that, in addition
to regularity-type and line separation, the manner of exploration could provide a
third, independent, and modality-specific cue to objectness. In our everyday
interactions we often explore and hold a single object in one of our hands. Thus, if
we feel two lines with two parts of one hand (here, the thumb and index finger) this
may be used as a cue that we are feeling two parts of the same object rather than
feeling two different objects. In contrast, we frequently touch and use two
different objects with our right and our left hands. Thus, if each of our index
fingers feels a different line, this may be used as a cue that we are feeling two
different objects. One-object interpretations of line pairs may therefore be more
consistent with one-handed exploration than two-handed exploration and vice versa
for two-objects interpretations. If so, then symmetry should be easier to detect for
one-handed exploration (since here cues from both regularity-type and exploration
would consistently indicate that one object was present) compared to two-handed
exploration (where cues about objectness would be conflicting) and vice versa for
repetition (which should be easier to detect with two-handed than one-handed
exploration).
Figure 8
A participant in Experiment 3 shown (A) using one hand to explore a pair
of irregular lines separated by 25 mm and, (B) using two hands to
explore a pair of repeated lines separated by 25 mm. Note that both
stimuli are oriented such that the axis of regularity is perpendicular to
the participant’s body midline. This contrasts to Experiments 1 and 2
where the stimuli were aligned with the body midline (see Figures 4 and 6). For the purpose of
these photographs, the curtain was raised to show the response labels which
reminded the participant which foot pedal to use. The black startpoint patch
is shown to the right of the stimulus (so it was on the left side for the
participant).
The design, stimuli, and procedure in Experiment 3 were identical to Experiment 2
except for the following points. Thirty-two students from the University of
Liverpool (22 females, mean age = 21 years,
SD = 3.8, range 18–31) volunteered to
take part in the experiment. All of the stimuli were rotated 90°
counterclockwise so that the orientation of the regularity was perpendicular to
the participant’s body midline. The frame that the stimuli were placed in
was also rotated 90° counterclockwise so the startpoint patch on which
participants rested their fingers at the beginning of each trial was on the left
side of the frame rather than on the top of the frame, see Figure 8. Participants started each trial by
moving their fingers from left to right rather than from top to bottom. Half of
the participants were instructed to explore the two lines simultaneously with
their two index fingers, as in Experiment 2. The remaining participants were
instructed to explore the two lines using their right hand only, with their
right index finger feeling the top line and their right thumb feeling the bottom
line, see Figure 8.No participant was replaced. There was one empty cell in the RT data for one
participant in the one-handed exploration group, which was filled by the mean
for that condition. As in Experiment 2, correct RT faster than 1 s or
slower than 35 s were removed as outliers (less than 1% of trials), and
ANOVAs were conducted on the mean correct RT and on the percentage of errors for
regular trials only.2 For clarity of presentation, we give the
results for the two exploration groups separately below. However, ANOVAs
comparing the two groups tested in Experiment 3, and ANOVAs comparing the
results of Experiment 2 to the two-handed exploration group in Experiment 3, are
given in the Appendix. Analyses of measures of sensitivity (d′) and bias
(c′) for each group are also given in the Appendix.
One-Handed Exploration Group
Participants used the thumb and index finger of their right hand to explore
stimuli that were oriented to be perpendicular to their body midline. There
were two within-participants factors: regularity-type (symmetry or
repetition) and line separation (small, medium, or large).Regularity-type was significant for both RT,
F(1, 15) = 6.32,
p = .02,
ηp2 = .30, and errors,
F(1, 15) = 5.89,
p = .03,
ηp2 = .28. We found the advantage
for symmetry detection (8.2 s, 14% errors) over repetition detection
(9.7 s, 20%) that we obtained in Experiment 2.Line separation was significant for both RT,
F(2, 30) = 30.54,
p < .001,
ηp2 = .67, and errors,
F(2, 30) = 13.54,
p < .001,
ηp2 = .47. Post hoc
Newman-Keuls analyses (p < .05) revealed
that regularity detection was harder for large separations (10.2 s,
29% errors) than for small (8.0 s, 7.5%) and medium (8.6 s,
14%) separations, with no significant difference between small and medium
separations.The interaction of Regularity-type × Line separation was
not significant for RT,
F(2, 30) = 1.30,
p = .3,
ηp2 = .08, but it was for errors,
F(2, 30) = 8.52,
p = .001,
ηp2 = .36, see Figure 9. To understand
this interaction we calculated the difference between regularity detection
for the largest (100 mm) compared to the smallest (25 mm) line
separation and conducted an ANOVA on these differences. This revealed that
the cost of increased line separation (100 mm–25 mm) on
accuracy was significantly less for symmetry (9% errors) than for repetition
(34%), F(1, 15) = 15.96,
p = .001,
ηp2 = .51. Note that this
pattern shows the reverse interaction to that which we found for vision in
Experiment 1 where the accuracy of repetition detection was more sensitive
to line separation than was symmetry detection.
Figure 9
Results for regular trials for the one-handed exploration group
in Experiment 3 for the haptic detection of symmetry (Sym) and
repetition (Rep) for line separations of 25 mm, 50 mm,
and 100 mm for RT (A) and errors (B). Error bars represent
one standard error of the mean.
Two-Handed Exploration Group
Participants used both of their index fingers to explore stimuli that were
oriented to be perpendicular to their body midline. There were again two
within-participants factors: regularity-type (symmetry or repetition) and
line separation (small, medium, or large).Regularity-type was significant for both RT,
F(1, 15) = 12.43,
p = .003,
ηp2 = .45, and errors,
F(1, 15) = 37.27,
p < .001,
ηp2 = .71. Symmetry detection
(13.2 s, 28% errors) was both slower and less accurate than
repetition detection (10.7 s, 9%). Note that this clear-cut advantage
for detecting repetition contrasts to both the symmetry advantage found here
in Experiment 3 for one-handed haptic exploration of across-body stimuli,
and the symmetry advantage found in Experiment 2, for two-handed haptic
regularity detection of body midline-aligned stimuli, as well as the
symmetry advantage found in Experiment 1, for visual regularity detection of
body midline-aligned stimuli.Line separation was significant for RT,
F(2, 30) = 5.38,
p = .01,
ηp2= .26, but not for errors,
F(2, 30) = 0.43,
p = .6,
ηp2 = .03. Post hoc Newman-Keuls
analyses (p < .05) revealed that
regularity detection was slower for large separations (12.6 s, 20%
errors) than for medium (11.4 s, 18%) and small (11.7 s, 18%)
separations, with no significant difference between medium and small
separations.The interaction of Regularity-type × Line separation was
not significant for RT,
F(2, 30) = 0.17,
p = .8,
ηp2 = .01, or for errors,
F(2, 30) = 1.18,
p = .3,
ηp2 = .07, see Figure 10, with a similar
slowing at larger separations for symmetry and repetition detection.
Figure 10
Results for regular trials for the two-handed exploration group
in Experiment 3 for the haptic detection of symmetry (Sym) and
repetition (Rep) for line separations of 25 mm, 50 mm,
and 100 mm for RT (A) and errors (B). Error bars represent
one standard error of the mean.
The main findings from Experiment 3 involved interactions between regularity-type
and three other factors: line separation, exploration type, and stimulus
orientation. We discuss each of these in turn. First, these results confirmed
the difference between haptic and visual regularity detection which we observed
when comparing the results of Experiments 1 and 2. For the two-handed
exploration group, effects of line separation were similar for symmetry
detection and for repetition detection, replicating the results for two-handed
haptic exploration in Experiment 2, see Figure 10. For the one-handed exploration group, line
separation influenced the accuracy of repetition detection more than that of
symmetry detection, see Figure
9. This interaction was the reverse of the interaction which we
observed for visual regularity detection, in Experiment 1, where increased line
separation disrupted the detection of symmetry more than repetition. For vision,
in Experiment 1, the results supported the hypothesis that small line
separations and symmetry provide consistent evidence for the presence of a
single object while large line separations and repetition provide consistent
evidence for the presence of multiple objects. However, this account was not
supported by the results for haptics, in Experiment 2 or 3.Second, regularity detection was strongly influenced by whether one or two hands
were used to explore across stimuli, where the axis of regularity ran
perpendicular to the body midline. Symmetry was easier to detect than repetition
for one-handed exploration whereas repetition was easier to detect than symmetry
for two-handed exploration. These results were consistent with our predictions
based on the hypothesis that both symmetry and one-handed exploration are cues
for the presence of one object, whereas both repetition and two-handed
exploration are cues for the presence of multiple objects.Third, considering only two-handed exploration, in Experiment 2 symmetry was
easier to detect than repetition when the axis of regularity of the stimuli was
aligned with the body midline. Thus, here we found the usual symmetry advantage.
In contrast, for the two-handed group in Experiment 3, repetition was easier to
detect than symmetry when the axis of regularity ran across the body midline.
This result suggests that, in Experiment 2 only, an egocentric, body-centered
(rather than an allocentric, world-centered) spatial frame of reference could be
used to represent stimuli aligned with the body midline. Here symmetry detection
was privileged relative to repetition detection because the axis of symmetry of
the stimuli was coincident with a reference frame based on the axis of bilateral
symmetry of the participant’s own body. Thus, the orientation of stimuli
relative to the body midline appears to play an important role in haptic
symmetry detection.We found an advantage for haptically detecting symmetry relative to repetition
for both two-handed exploration of midline-aligned stimuli in Experiment 2, and
for one-handed exploration of across-body stimuli in Experiment 3. Thus, an
advantage for haptic detection of repetition occurred only when
both the manner of exploration was consistent with a
two-objects interpretation of the stimulus (i.e., two-handed exploration,
favoring repetition detection) and when participants could not
easily take advantage of body-centered spatial frames of reference (for across
stimuli, where the axis of symmetry of stimuli was perpendicular to the axis of
bilateral symmetry of the participant’s own body). Thus, in general,
symmetry appears to be easier to detect than repetition for haptics, consistent
with what has long been established for vision (Julesz, 1971).
General Discussion
The present studies investigated two issues. First, we used truly repeated rather
than anti-repetition stimuli to seek evidence for the claim that there is a
one-object advantage for detecting symmetry and a two-objects advantage for
detecting repetition (Koning &
Wagemans, 2009; Van der Helm
& Treder, 2009). Second, we investigated whether effects found for
regularity detection reflect internal, modality-specific processing or if they
reveal differences arising directly from the presence of regularities out in the
external, physical world. The overall motivation for examining these issues was to
gain insights into what it means to be an object in vision and in touch. We
manipulated three different potential cues to objectness: the type of regularity
being detected, the separation between task-critical lines, and whether one hand
versus two hands felt stimuli in haptic tasks. We hypothesized that symmetry, small
line separations, and one-handed exploration would all provide evidence that a
single object was present, whereas repetition, large line separations, and
two-handed exploration would all provide evidence that two objects were present. Our
results revealed that regularity detection is strongly influenced by all three
possible cues to objectness, and that these effects are modulated by the modality of
stimulus presentation, and, for haptics, by the ease of use of egocentric,
body-centered spatial reference frames. We found the predicted interaction of
objectness by regularity-type in some, but not all, cases and this depended on
whether stimuli were presented visually or haptically, as detailed below. We argue
that these effects on regularity detection may mainly inform us about
modality-specific encoding and processing strategies used by vision and touch and,
thus, that they may not reflect intrinsic properties of objects in the physical
world. Three of our results support this claim.First, we compared line separation effects for haptic and visual regularity
detection. In the context of visual perception, it has often been claimed that
symmetry is used as a cue for the presence of a single, bilaterally symmetric
object, while repetition is used as a cue for the presence of multiple, similarly
shaped objects (Koning & Wagemans,
2009; Van der Helm &
Treder, 2009). These claims are plausible but, as reviewed in the
Introduction, there is surprisingly little evidence for them. For line separation we
investigated a novel prediction that during regularity detection our perceptual
processes may take advantage of the fact that pairs of nearby lines are more likely
to belong to a single object whereas pairs of more distant lines are more likely to
belong to two different objects.For vision, in Experiment 1, we found the predicted interaction between
regularity-type (symmetry vs. repetition) and the distance between lines. For
vision, in Experiment 1, the cost of increased line separation was greater for
symmetry than for repetition. This was as predicted since nearby, symmetrical lines
provide consistent cues that a single object is present, whereas these cues are in
conflict for well-separated, symmetrical lines. The opposite predictions were made
for repetition, with well-separated, repeated lines providing consistent cues that
multiple, similar objects are present, whereas these cues are in conflict for
nearby, repeated lines. The results of Experiment 1 are consistent with our previous
findings using symmetrical and anti-repetition planar shapes (see Figure 2) where visual symmetry was
easier to detect for one-object (as opposed to two-objects) stimuli and the reverse
was true for repetition (Cecchetto &
Lawson, 2016).In contrast, for haptics, in Experiments 2 and 3, there was an overall advantage for
detecting regularities across pairs of nearby (as opposed to well-separated) lines,
but no reliable interaction between regularity-type and line separation. Instead,
the cost of increased line separation was similar for symmetry and for repetition
detection, except for the one-handed group in Experiment 3. In this latter case, the
opposite interaction was found to that observed for vision, namely a greater
advantage for nearby lines for detecting repetition than for symmetry. Again, these results are
similar to our previous findings using planar shapes (Cecchetto & Lawson, 2016), where regularities
were easier to detect within a single object (as opposed to across two objects) for
both symmetry and repetition in haptics.Thus, in both the present studies and in Cecchetto and Lawson (2016), we reliably found the predicted interaction
between objectness and regularity-type for vision, but not for haptics. For vision,
but not for haptics, these results are consistent with small line separations and
symmetry providing consistent cues that a single object is present while large line
separations and repetition provide consistent cues that two objects are present. We
do not, as yet, have a good account of why vision and touch behave differently in
this case. To address this issue, we have conducted further studies in which we have
manipulated the time course of presentation of stimuli to vision and whether stimuli
are presented all at once, or are viewed through a moving aperture (Cecchetto & Lawson, 2015).Second, we tried to manipulate perceived objectness by changing how participants
haptically explored the stimuli. We reasoned that pairs of lines explored with one
hand are more likely to be interpreted as belonging to a single object, whereas
pairs of lines explored with two separate hands may be more likely to be interpreted
as belonging to two different objects.To test this hypothesis, in Experiment 3 we compared haptic regularity detection of
across stimuli using the index fingers of both hands, versus using the thumb and
index finger of the right hand. Averaging over the effects of line separation,
symmetry was easier to detect than repetition for one-handed exploration whereas the
reverse was true for two-handed exploration. This result is consistent with
one-handed exploration and symmetry providing consistent cues that a single object
is present while two-handed exploration and repetition provide consistent cues that
two objects are present, making regularity detection easier overall in both cases.
In contrast, regularity detection was harder overall when cues provided conflicting
information about the number of objects present (for one-handed exploration of
repetition, and for two-handed exploration of symmetry).Regularity detection is probably also influenced by other aspects of haptic
exploration which were not manipulated experimentally in the present studies. From
pilot testing, and informal observation, it appears that regularity detection
depends critically on aligning in time the inputs from exploring two, matched parts
of a regular stimulus. In addition, the position of a finger on a contour or line
(on the left or right side or on top) may influence how the shape of that edge is
perceived. Future research should test how such changes in exploration strategies
may influence the detection of regularities and the perception of objectness.Third, we compared two-handed haptic regularity detection for stimuli aligned to the
body midline of the participant (Experiment 2) and for stimuli rotated so that the
axis of regularity ran perpendicular to the body midline (Experiment 3). Symmetry
was easier to detect than repetition for stimuli aligned with the body midline.
Here, the body’s own axis of bilateral symmetry provided a salient spatial
frame of reference which was aligned with the axis of regularity of symmetrical
stimuli. In contrast, repetition was easier to detect than symmetry when there was
no privileged reference frame for symmetry detection because- the axis of regularity
ran across the body midline.Across all three of these comparisons, the same symmetrical and repeated stimuli were
presented at the same line separations. Only the manner of processing differed
across conditions (modality: vision vs. haptics; manner of haptic exploration:
one-handed vs. two-handed; and orientation relative to the body midline: aligned vs.
across). Although the physical stimuli presented were not altered by these three
manipulations, each had a clear effect on regularity detection, indicating the
powerful influence of differences in perceptual encoding and processing.Finally, we should highlight the fact that although in our studies we propose that we
have manipulated several potential cues to objectness, even in vision, it has proven
difficult to provide a formal definition of objectness (Feldman, 2003), while in haptics this topic does
not appear to have been addressed at all. We do not claim that we have objectively
varied objectness nor do we consider that objectness is a clear-cut, all-or-nothing
attribute of stimuli. Previous studies which investigated the interaction between
regularity detection and objectness using anti-repetition (Baylis & Driver, 1995; Bertamini, 2010; Bertamini et al., 1997; Cecchetto & Lawson, 2016; Koning & Wagemans, 2009) used a mixture of cues to define
objectness including closure, regularities, color, luminance, 3D projections, and
stratification in depth to distinguish one-object from two-objects stimuli.
Consistent with this approach, we suggest that multiple cues to objectness are
extracted from perceptual inputs. Our results show that, in addition to those cues
listed above, line separation and manner of exploration may play a significant role
in specifying objectness. An important issue for future research will be to try to
understand the relative importance of these cues in determining objectness, how they
are combined and how any conflicts between them are resolved. In particular, the
manipulations used in the present studies provide a promising means of investigating
how objectness is specified for our sense of touch.In conclusion, we found several interactions consistent with the predictions of an
account that proposes that regularity-type, line separation, and manner of
exploration can all influence regularity detection because they are all informative
about the nature of objectness. In contrast to the results for vision, the results
for the interaction of regularity-type by line separation for haptics did not
support this account. It is not clear why we did not obtain the latter interaction,
but this result seems reliable, given that we obtained a similar result when
objectness was manipulated more directly, using planar shapes and anti-repetition
(Cecchetto & Lawson, 2016,
see Figure 2), rather than line
separation and true repetition as used here. Together, these results inform us
about, first, what cues may be used to determine objectness (regularity-type and
line separation for vision; regularity-type and manner of exploration for haptics)
and, second, what we can learn from effects on regularity detection. First, these
results support the proposal that symmetry, small line separations (for vision but
not haptics), and one-handed exploration (for haptics) are all used as cues that a
single object is present, while repetition, larger line separations (for vision but
not haptics), and two-handed exploration (for haptics) are all used as cues that
multiple objects are present. Regularity detection was influenced by all of these
potential cues to objectness as well as by the spatial reference frame that could be
used to represent the stimuli. Second, these results suggest that effects on
regularity detection do not primarily reflect intrinsic, structural properties of
physical objects in the world. Several of our manipulations had clear effects on
regularity detection despite causing little or no change to physical properties of
the stimuli, namely the modality of presentation, the manner of exploration, and the
availability of egocentric reference frames. Our findings instead suggest that
regularity detection effects may be most informative about modality-specific
differences in how stimuli are encoded and processed across vision and touch. This
conclusion is consistent with the claims of Feldman (2003) that understanding the nature of objectness will
involve specifying how our subjective, internal, perceptual representations are
organized, rather than informing us about how the objective, external world is
structured.