 |
Previous Article | Next Article 
The Journal of Neuroscience, July 15, 2001, 21(14):5289-5296
Temporal Cues Contribute to Tactile Perception of Roughness
Carissa J.
Cascio and
K.
Sathian
Department of Neurology, Emory University School of Medicine,
Atlanta, Georgia 30322
 |
ABSTRACT |
Optimal perception of surface roughness requires lateral movement
between skin and surface, suggesting the importance of temporal cues.
The roughness of periodic gratings is affected by changing either
inter-element spacing (groove width, G) or element width (ridge width, R). Peripheral neural responses to
gratings depend quantitatively on a spatial variable, G,
and a temporal variable, grating temporal frequency
(Ft), with changes in
R acting indirectly through concomitant changes in
Ft. We investigated, psychophysically, the
contribution of temporal cues to human tactile perception of roughness,
using gratings varying in either R or G.
Gratings were scanned across the immobile fingerpad with controlled
movement speed (S) and contact force. In one experiment,
we found that roughness magnitude estimates depended on both
G and Ft. In a second
experiment, discrimination of the roughness of gratings varying in
either R or G was affected by
manipulating Ft. Overall, the effect of
G on roughness judgments was much stronger than that of
Ft, probably explaining why many
previous studies using surfaces that varied only in inter-element
spacing led to the conclusion that temporal factors play no role in
roughness perception. However, the perceived roughness of
R-varying gratings was determined by
Ft and not spatial variables. Roughness
judgments were influenced by G and
Ft in a manner entirely consistent with
predicted afferent response rates. Thus perceived roughness, like
peripheral afferent responses, depends in part on temporal variables.
Key words:
human; perception; somatosensory; touch; finger; texture; gratings; roughness; temporal frequency; psychophysics; discrimination; magnitude estimation
 |
INTRODUCTION |
Surface roughness is particularly
salient to the tactile sense (Klatzky et al., 1987 ) and is better
assessed using touch than vision (Heller, 1989 ). Tactile roughness
perception is commonly studied using periodic surfaces such as gratings
of alternating ridges and grooves, or dot patterns (Sathian, 1989 ;
Johnson and Hsiao, 1992 ). Perceived roughness increases with increasing
inter-element spacing, grating groove width
(G) (Lederman and Taylor, 1972 ; Sathian et
al., 1989 ), or dot spacing (Connor et al., 1990 ; Connor and Johnson,
1992 ; Meftah and Chapman, 2000 ) and less markedly with decreasing
element width, grating ridge width (R)
(Lederman and Taylor, 1972 ; Sathian et al., 1989 ). Optimal
discrimination of textures requires lateral motion (Meenes and Zigler,
1923 ; Krueger, 1970 ; Morley et al., 1983 ; Lederman and Klatzky, 1987 ; Gamzu et al., 2000 ; Hollins and Risner, 2000 ), which introduces a
temporal dimension and thus the possibility that temporal factors are
important. Yet, temporal cues are generally considered unimportant to
roughness judgments, except for very fine surfaces (Srinivasan et al.,
1990 ; Hollins and Risner, 2000 ), because neither changes in movement
speed (S) (Lederman, 1974 ; Kudoh, 1988 ; Meftah and Chapman, 2000 ) nor pre-adaptation by vibrotactile stimuli (Lederman et
al., 1982 ) seem to affect roughness magnitude estimates greatly.
Temporal factors do affect, however, neural responses to gratings.
Peripheral afferents fire in bursts phase-locked to grating temporal
frequency (Ft) (Darian-Smith and Oke,
1980 ; Morley and Goodwin, 1987 ), so that their temporal firing patterns
reflect grating periodicity.
Since:
|
(1)
|
Ft increases as S
increases or as either G or R decreases. At
constant S, the number of impulses per afferent burst
(Iburst) is influenced by altering
either G or R; however, when S is
covaried with G or R to keep
Ft constant,
Iburst still depends on G
but is now invariant with R (Goodwin et al., 1989 ). Hence,
changing R affects peripheral afferent responses only
indirectly through associated changes in
Ft. The dependence of
Iburst on G and
Ft is given by:
|
(2)
|
where a, b, and c are constants the values of which differ between
afferent types (Goodwin et al., 1989 ).
Mean firing rate (Is) is the product
of Ft and
Iburst, hence:
|
(3)
|
The representation of grating periodicity is preserved in the
temporal firing patterns of thalamic (Sinclair et al., 1991 ) and
primary somatosensory cortical neurons (Sinclair and Burton, 1991a ;
Sinclair et al., 1996 ).
The precise neural encoding of temporal variables conflicts with the
idea that these variables do not contribute to perceived roughness. We
therefore reinvestigated the contribution of temporal cues to roughness
judgments, using gratings (Fig.
1A) varying in either
element width (R) or spacing (G).
On the basis of neurophysiological findings reviewed above, we
hypothesized that temporal variables contribute to roughness judgments.
An alternative hypothesis is that these variables are filtered out by
neural processing and do not influence roughness perception. Our aim
was to distinguish between these two competing hypotheses. We sought
convergent evidence using two psychophysical approaches: roughness
magnitude estimation and roughness discrimination.

View larger version (20K):
[in this window]
[in a new window]
|
Figure 1.
A, Cross-sectional view of a
periodic grating. G, Groove width; R,
ridge width; spatial period = G + R.
B, C, Trial structures in the magnitude
estimation (B) and discrimination
(C) experiments. For magnitude estimation, two
successive trials are shown. For discrimination, the two scans
comprising a single trial are shown. The subject responded verbally
after each trial. ME, Magnitude estimate;
ISI, interscan interval.
|
|
Preliminary reports of our findings have been published previously in
abstract form (Cascio and Sathian, 2000a ,b ).
 |
MATERIALS AND METHODS |
Subjects. Thirty-two task-naïve subjects
(mean age, 25.4 years; range, 16-49 years) were recruited from the
Emory University community and compensated at an hourly rate. None had
a history of trauma affecting the hand or its innervation,
developmental or neurological disorders, or fingertip calluses.
Separate groups, each comprising 16 subjects (10 female and 6 male),
participated in two different experiments. All procedures were approved
by the Human Investigations Committee of Emory University.
Gratings. Gratings were rectangular in shape, measuring
80 × 40 mm, and consisted of periodic trapezoidal patterns of
alternating ridges and grooves (Fig. 1A) photo-etched
in steel-backed plastic, manufactured as described previously (Sathian
and Zangaladze, 1997 ). There were two sets of gratings. In one set,
G was constant at ~1 mm (actual values, 0.97-1.02 mm),
and R varied from 0.5 to 1.95 mm. In the other set,
R was constant at ~0.2 mm (actual values, 0.16-0.2 mm),
and G varied from 0.75 to 1.97 mm.
Tactile stimulation. The subject was seated comfortably with
the right forearm supine and extended forward; the index finger was
immobilized using adhesive tape. Auditory cues were excluded using
earplugs and pink noise played through headphones; visual cues were
screened out. Gratings were scanned across the index fingerpad by a
custom-built stimulator comprising dual servo-controlled actuators. One
actuator controlled S, the horizontal speed of grating
motion. Both speed and position were monitored optically. The other
actuator worked in the vertical plane to apply the gratings normal to
the fingerpad with controlled contact force, sensed by a strain gauge
system. The two actuators were coupled such that the action of the
horizontal actuator (HA) resulted in horizontal translation of the
vertical actuator (VA) to the desired position. The grating used on a
particular scan was chosen from a collection of gratings arranged on a
holding shelf. Before each scan, the HA moved the VA from its home
position to a specified position directly above a particular grating.
The VA picked up the selected grating electromagnetically and held it
on a plate on its lower surface. After grating pickup, the HA moved the
VA to a specified position so that one end of the grating would be
directly over the fingerpad. At this point the VA was activated in
displacement-control mode causing it to move down until it contacted
the fingerpad. When contact was sensed by the force sensors, the VA was
switched into force-control mode. The grating was then scanned once
from left to right across the long axis of the finger by the dual
action of the HA and VA, at the specified values of S and
contact force. Scan length was equal to grating length, 80 mm. On
completion of the scan, the VA was lifted off the fingerpad and moved
back over the grating holding shelf, where the electromagnet was
de-energized to allow the grating to drop back into its stowed
position. The VA then returned to its home position to complete the
cycle. The stimulator was operated using custom software running on two
linked PCs, via a Labview user interface within which trial sequences were automated. On the basis of measured samples of S and
force, variability in S and contact force did not exceed
±0.4 mm/sec and ±2.5 gm, respectively, from the specified values.
Experiment 1: roughness magnitude estimation. Subjects rated
the perceived roughness of gratings varying in either G or
R. For the R-varying set, three gratings were
chosen, with R values of 0.5, 1.17, and 1.95 mm. Three
gratings were also selected from the G-varying set, with
G values of 0.75, 1.22, and 1.97 mm. To avoid reliance on
irrelevant cues such as minor irregularities on individual gratings,
multiple copies of each grating were used in rotation (three copies of
the grating with the largest value of G or R and
two copies for the others). Each subject participated in two sessions,
one with G-varying gratings and the other using R-varying gratings. Session order was counterbalanced across
subjects. In each session, each grating was presented at three values
of S: 30, 45, and 68 mm/sec for gratings varying on
G and 35, 50, and 70 mm/sec for those varying on
R. The values of S, G, and R were chosen so that different combinations of S
and the spatial variables yielded nearly the same
Ft (Table
1). This design allowed us to examine the
relative contributions of each of the four
variables Ft, S,
G, and R to roughness ratings. If
Ft were the primary determinant of
roughness, then gratings with near-identical values of
Ft would be rated as similar in
roughness, regardless of spatial parameters. On the contrary, if
Ft and other temporal variables were
of no consequence, perceived roughness would depend only on spatial parameters (G or R). Contact force was held
constant at 80 gm in this experiment.
Subjects were instructed to rate each grating for roughness using a
scale of their choice. Each trial consisted of a single scan of a
grating across the fingerpad (Fig. 1B). The subject then called out a number representing the roughness of that grating. The number was manually recorded. Each session began with a block of 18 practice trials comprising two presentations of each of the nine
combinations of S and grating, in pseudorandom order. During
this block, the subject was told to select and adjust a scale for
roughness. The data from this block were not analyzed. In the remainder
of the session, subjects were presented 10 similar blocks for a total
of 180 trials, 20 for each of the 9 combinations. The magnitude
estimates from these trials were normalized across subjects by dividing
each estimate for a particular subject by the grand mean of all
estimates for that subject. Because roughness ratings for G-
and R-varying gratings were made in separate sessions, and
subjects were not asked to use the same scales between sessions, the
magnitude estimates were treated as independent for each series.
Repeated-measures, mixed-model ANOVAs with normalized magnitude
estimate as the dependent variable, and S and G
or R as independent variables, together with
Bonferroni-corrected paired t tests, were used to assess the
statistical significance ( = 0.05) of the results. There were three
pairwise comparisons between the magnitude estimates for the three
values of S at each of the three values of G or
R. Similarly, there were three pairwise comparisons at each
value of S between the magnitude estimates for the three values of G or R. Hence, the Bonferroni
correction required p values of 0.0028 for significance for
each of these 18 pairwise comparisons (per grating set). In
examining the effect of Ft, pairwise
comparisons were restricted a priori to magnitude estimates at the same Ft, because the key
question was whether these would differ. Thus, the Bonferroni
correction required p values of 0.01 for significance for
each of these five comparisons (per grating set).
Experiment 2: roughness discrimination. Subjects
discriminated a standard from a comparison grating, based on roughness.
A baseline condition, in which both gratings were scanned at constant S (CS), was compared with two other conditions in which
S was altered. In a constant
Ft (CF) condition, the comparison
grating, with the smaller R or G, was scanned at
a slower S so that Ft was
equal for the two gratings. If Ft is a
critical variable, this should impair discrimination performance. To
control for a potentially confusing effect of varying S, a
third condition was included in which the speed changes were in the
opposite direction to that in the CF condition. The grating with the
smaller R or G was scanned faster in this
condition, thereby exaggerating the difference in
Ft between the two gratings. We refer
to this as the exaggerated Ft
difference (EFD) condition.
Each subject ran in four sessions, one pair each for R and
G discrimination, with the R versus G
order counterbalanced across subjects. In each trial, the subject was
presented sequentially with a standard and a comparison grating, each
scanned once (Fig. 1C). The subject was instructed to
identify, in a two-interval forced choice, the rougher grating when
performing R discrimination and the smoother for
G discrimination. Because grating roughness rises with
decreasing R but declines with decreasing G
(Lederman and Taylor, 1972 ; Sathian et al., 1989 ), the target was
always the comparison grating, which had a smaller R or
G. The subject's verbal response was recorded manually. One
of three copies of the standard was rotated into use on successive
trials, for the same reason as in experiment 1.
S was constant (65 mm/sec) during the first session for each
grating set. This session began with a demonstration trial using the
standard and a midrange comparison; the subject was informed which
interval (first or second) contained the target. Next, a sequence of
comparison gratings was presented, starting with easy and proceeding to
more difficult comparisons using a staircase procedure that converges
on the 71% correct threshold (Levitt, 1971 ). One purpose of this
sequence was to allow practice; hence, feedback was given during this
phase but not during subsequent testing. The second purpose of this
sequence was to select one to two comparison gratings that would yield
80-95% accuracy in the ensuing CS condition, during which subjects
performed a 20-trial block for each grating. Gratings on which actual
performance was 80-95% were used further in the second session (one
grating for most subjects, occasionally two). For G
discrimination, most selected gratings were close in G to
the standard (G: standard = 1.97 mm; comparisons = 1.22-1.82 mm). There was a more even distribution of gratings across
the range for R discrimination (R: standard = 1.95 mm; comparisons = 0.5-1.6 mm), attesting to the greater difficulty of this task (Sathian and Burton, 1991 ). The second session
consisted of the two conditions under which S was altered, the CF and EFD conditions, with 20 randomly interleaved trials per
condition. When multiple gratings were used in the second session, all
trials for one were completed before proceeding to the next. Contact
force was held constant at 40 gm in this experiment.
Statistical analysis compared mean accuracy in the CF and EFD
conditions with that in the baseline (CS) condition, using paired, two-tailed t tests ( = 0.05), Bonferroni corrected by
requiring p = 0.025 for significance, given two planned
comparisons in each data set.
 |
RESULTS |
Experiment 1: roughness magnitude estimation
Effect of S
Figure 2A
illustrates that, for the R-varying set, roughness for a
given grating rose by almost one-sixth as S doubled. At each
speed, roughness fell by one-fourth as R quadrupled. ANOVA demonstrated significant main effects (p < 0.0001) on roughness of both S
(F(2,320) = 35.9)
and R
(F(2,320) = 73.7)
without a significant interaction
(F(4,320) = 1.15, p = 0.33). In keeping with this, roughness ratings differed significantly
on seven of nine pairwise comparisons for different values of
S at a given R and on all nine pairwise
comparisons for different R values at the same S.

View larger version (12K):
[in this window]
[in a new window]
|
Figure 2.
Mean normalized roughness magnitude estimates as a
function of speed (S) for gratings varying in
R (A) and G
(B). Values of the variable parameter are given
on the right of each graph. Standard errors are too
small to be shown here and are given in Table 2.
|
|
Roughness ratings for G-varying gratings also tended to
increase with S (Fig.
2B). G had a
much larger effect than R, with roughness at any given speed
tripling as G nearly tripled. ANOVA showed that the effects
of both G (F(2,320) = 938.9) and S (F(2,320) = 16.0) were
significant (p < 0.0001), with a significant
interaction (F(4,320) = 5.63, p = 0.0002) accounted for by the absence of a
significant speed effect at the narrowest G. Pairwise
comparisons of roughness estimates revealed that the effects of
S for G-varying gratings were less consistent
and, in general, smaller than for R-varying ones, with
significant differences on only three of nine comparisons for different
values of S at a given G. In contrast, all nine
pairwise comparisons for different G values at the same S yielded significant differences.
Effect of
Ft
To examine the effect of Ft, the
data of Figure 2 were replotted in Figure
3 as a function of
Ft. For R-varying gratings, there was a clear effect, comprising a roughness increase by
approximately one-half for a quadrupling of
Ft (Fig. 3A). The
clustering of points in Figure 3A for which values of
Ft were almost identical, despite
disparate values of R and S, indicates that the
roughness of this series of gratings depends principally on
Ft rather than R or
S. This was verified by pairwise comparisons of roughness ratings for the five same-Ft pairs:
only two significant differences were found, both minute differences
involving one roughness estimate (identified by an asterisk
in Fig. 3A).

View larger version (8K):
[in this window]
[in a new window]
|
Figure 3.
Mean normalized roughness magnitude estimates as a
function of temporal frequency (Ft)
for gratings varying in R (A) and
G (B). Symbols as in Figure 2.
Asterisk in A identifies the only
estimate for R-varying gratings that differed
significantly from other estimates at the nearly identical
Ft.
|
|
In contrast, a plot of roughness versus
Ft for G-varying gratings
(Fig. 3B) revealed no clustering based on
Ft. All five pairwise comparisons
between roughness ratings at the same
Ft values yielded substantial and
significant differences. For example, the most extreme roughness
magnitude estimates of 1.6 and 0.5 were evoked by nearly identical
Ft values of 31.6 and 31.9 Hz. The
plot in Figure 3B is very similar to that in Figure
2B, demonstrating a large positive effect of
G (note the wide separation between the different symbols)
and a small positive effect of S or
Ft for each grating except the one
with the smallest value of G.
Relationship of roughness magnitude estimates to
neural responses
This experiment demonstrates that both of the stimulus variables
that determine peripheral afferent response, G and
Ft, also affect perceived roughness,
in keeping with our hypothesis. If perceived roughness is
quantitatively related to the neural responses of monkey peripheral
afferents expressed in Equation 3, then it should vary with changes in
Ft that result from variations in either S or grating spatial parameters (G or
R). Because of the complex relationship between firing rate
(Is) and the stimulus variables
G and Ft, and the
interdependence of these two stimulus variables, the direction in which
Is changes with
Ft is not constant. Thus,
Is may either increase or decrease as
Ft rises. Moreover, the nature of the
relationship varies between afferent types. It is therefore helpful to
consider the effect of variation in stimulus parameters, within the
range used in this experiment, on the value of
Is predicted from Equation 3. Figure
4 illustrates the relationship between
predicted Is and
Ft for each afferent population
innervating the monkey fingerpad: slowly adapting type I (SA), rapidly
adapting (RA), and Pacinian (PC) afferents. Predicted Is was derived from Equation 3 at each stimulus
condition used in this experiment, using the values for the constants
computed by Goodwin et al. (1989) for each afferent class. This neural measure increases with Ft for
R-varying gratings, when G is constant, regardless of whether changes in Ft
result from changes in S or R (Fig.
4A-C). For the G-varying
series of gratings (R constant), however, the situation is
more complicated (Fig. 4D-F).
Predicted Is tends to rise with
Ft when S is varied for a
given grating. When G is varied, its effect on
Is is dominant and tends to override that of Ft. The resemblance of the
plots of Figure 4 to the corresponding data of Figure 3 is striking. It
suggests that perceived roughness is strongly tied to peripheral
afferent response rates.

View larger version (20K):
[in this window]
[in a new window]
|
Figure 4.
Predicted afferent firing rates
(Is), for the conditions used in the
magnitude estimation experiment, as a function of temporal frequency
(Ft) for gratings varying in
R (A-C) and
G (D-F).
SA, Slowly adapting type I afferents; RA,
rapidly adapting afferents; PC, Pacinian afferents.
Symbols as in Figure 2.
|
|
Figure 5 plots the mean roughness
magnitude estimates observed in this experiment against the predicted
values of Is depicted in Figure 4.
When R was the independent variable, roughness was highly
correlated with Is for all three
afferent classes (Fig. 5A-C). The
correlation was slightly higher for RAs and PCs (r = 0.97 for both) (Fig. 5B,C) than for
SAs (r = 0.94) (Fig. 5A). When
G was the independent variable, roughness correlation with Is varied between afferent classes,
being best for SAs (r = 0.98) (Fig.
5D), poorest for RAs (r = 0.63) (Fig.
5E), and intermediate for PCs (r = 0.82) (Fig. 5F). The strength of these correlations confirms that there is a quantitative relationship between perceived roughness magnitude estimates and the peripheral neural response rates
modeled mathematically by Equation 3. The concept of a universal linear
relationship between perception and neural response (Johnson et al.,
1996 ) certainly fits with our data. However, we cannot exclude the
possibility of a non-linear relationship, especially in the case of RA
and PC responses to G-varying gratings.

View larger version (24K):
[in this window]
[in a new window]
|
Figure 5.
Scatter-plots of mean roughness magnitude
estimates versus predicted afferent firing rates
(Is), for the conditions used in the
magnitude estimation experiment, for gratings varying in
R (A-C) and
G (D-F).
Correlation coefficients are indicated above each plot.
SA, RA, and PC are as in
Figure 4.
|
|
Experiment 2: roughness discrimination
Effects of holding Ft constant and
exaggerating Ft differences
As Figure 6A
shows, discrimination of grating roughness based on R was
greatly impaired by holding Ft
constant. Accuracy declined from 83% in the baseline, CS condition to
63% in the CF condition, a significant difference
(t(18) = 3.86; p = 0.001). Individually, all but 2 of 16 subjects showed this predicted
impairment. In the EFD condition, in which
Ft differences between gratings were exaggerated relative to the CS condition, discrimination accuracy was
slightly higher but not significantly different from baseline (t(18) = 1.07; p = 0.3). This indicates that the lower accuracy in the CF condition was
not simply the result of confusion engendered by changing
S.

View larger version (17K):
[in this window]
[in a new window]
|
Figure 6.
Mean discrimination accuracy for gratings varying
in R (A) and G
(B). CS, Constant speed condition;
CF, constant Ft condition;
EFD, exaggerated
Ft-difference condition.
Asterisks identify significant differences from the CS
(baseline) condition. Error bars represent SEMs.
|
|
The results for G-varying gratings contrasted with those for
R-varying gratings. Holding
Ft constant resulted in slightly better roughness discrimination than at baseline for gratings varying
in G (Fig. 6B), but there was no
significant difference in performance between CS and CF conditions
(t(18) = 1.08; p = 0.29). However, accuracy fell from a baseline of 83% to 75% in the
EFD condition (Fig. 6B). Although this difference was
smaller than that noted for R variation in the CF condition,
it was significant (t(18) = 2.74;
p = 0.01).
Relationship of discriminative performance to neural responses
If roughness perception is based on the stimulus-response
relationship of Equation 3, then holding
Ft constant should clearly impair
roughness discrimination for R-varying gratings. Because of
the dominant effect of G, this effect should be smaller for G-varying gratings. Our results, in accord with these
predictions, indicate that Ft is a
crucial determinant of the roughness of R-varying gratings
and also influences roughness for G-varying gratings. Figure
7 displays the differences in predicted
Is between the standard grating and
the most commonly used comparison grating in each series, for each of
the three conditions (CS, CF, and EFD) and each afferent class.
Comparison of Figure 7 with Figure 6 reveals that the differences in
predicted Is of all three afferent types bear the same relationship between conditions as the
corresponding performance values. Specifically, the significant
declines in accuracy (relative to baseline) in the CF condition for
R-varying gratings (Fig. 6A) and in the
EFD condition for G-varying gratings (Fig.
6B) correspond to similar declines in the predicted
Is differences (Fig. 7). In the case
of R-varying gratings, this is easily appreciated for all
three afferent types (Fig. 7A-C). For
G-varying gratings, this is easier to discern for RAs (Fig.
7E) and PCs (Fig. 7F) than for SAs (Fig.
7D), although SAs also show the same trend. Therefore,
roughness discrimination performance is well accounted for by the
afferent responses modeled in Equation 3, buttressing the hypothesis
that Ft, along with G,
affects grating roughness.

View larger version (31K):
[in this window]
[in a new window]
|
Figure 7.
Predicted differences between afferent firing
rates (Is) to the standard grating
and most commonly used comparison grating in the discrimination
experiment. A-C,
R-varying gratings: Is for
standard (smoother) grating subtracted from
Is for comparison (rougher) grating, values
shown for comparison grating with R = 1.3;
D-F, G-varying gratings:
Is for comparison (smoother) grating
subtracted from Is for standard (rougher)
grating, values shown for comparison grating with G = 1.82. SA, RA, and PC are
as in Figure 4; CS, CF, and
EFD are as in Figure 6. Note that
Is differences in the CF condition for
R-varying gratings, which lie between 0.1 and 0, are
too small to be discerned.
|
|
 |
DISCUSSION |
Because optimal tactile perception of roughness depends on
movement (Meenes and Zigler, 1923 ; Krueger, 1970 ; Lederman and Klatzky,
1987 ; Hollins and Risner, 2000 ), the associated neural activation is
distributed in both time and space. This makes it likely, a priori,
that the nervous system uses both spatial and temporal stimulus
variables to encode surface texture. Our findings, consistent with our
hypothesis, demonstrate that temporal cues do indeed contribute to
tactile texture perception. This enables rejection of the alternative
hypothesis, that temporal variables are unimportant because they are
filtered out neurally.
The two tasks we used are complementary. Magnitude estimation depends
on observations that are subjective but unbiased by the experimenter.
In the discrimination experiment, assessment was objective but
roughness was experimenter defined. The results of both experiments
converge on the conclusion that perceived roughness, like peripheral
afferent responses, depends on G, a spatial variable, and
Ft, a temporal variable. Moreover,
changes in perceived roughness resulting from varying stimulus
parameters, over the range used, are completely predictable from
corresponding changes in peripheral afferent response rates computed
from Equation 3. The overall conclusions of the present study are not
critically dependent on our choice of particular stimulus parameters
for the following three reasons. First, the effects of G and
R on roughness are fairly uniform over spatial periods
ranging from 0.75 to 3 mm, with no apparent interaction effect (Sathian
et al., 1989 ). Second, Goodwin et al. (1989) showed that Equation 2,
from which Equation 3 derives, generalizes over a wide range of
stimulus conditions (spatial periods of 0.75-3 mm and movement speeds
15-480 mm/sec). Third, peripheral afferent response rates are
unaffected by the ratio G/R when this is varied
explicitly (Sathian, 1987 ). Our study used precisely controlled,
passive, linear motion, because it is easiest to study the effect of
Ft under such conditions. However, the
findings probably also apply to active movement, because roughness
ratings are similar whether movement is active or passive (Lederman,
1981 ), and movement parameters are quite well controlled even during
active tactile judgments of textures (Morley et al., 1983 ).
Roughness magnitude estimation
The present study establishes that roughness magnitude estimates
of gratings depend in part on Ft. For
R-varying gratings, Ft was
the principal determinant of roughness. In the case of G-varying gratings, the large effect of G
dominated over the weaker effect of
Ft. Roughness ratings were highly
correlated with SA afferent response rates regardless of whether
R or G was varied. PC and RA afferent response
rates correlated very well with roughness ratings when R was
varied (and Ft determined roughness)
but less well when G was varied.
Our study confirms the well known observation that G affects
perceived roughness more powerfully than R (Lederman and
Taylor, 1972 ; Sathian et al., 1989 ) and suggests that this is because of the relative strengths of the G and
Ft effects. The present study
contradicts previous studies reporting that temporal factors are of no
consequence for roughness magnitude estimates (Lederman, 1974 ; Lederman
et al., 1982 ; Meftah and Chapman, 2000 ). One reason for this
discrepancy is our inclusion of surfaces distinguished by changes in
element width (R), which elicited the clearest
temporal effects, whereas the earlier studies varied inter-element
spacing (G or dot spacing). Although we found temporal
effects even when G was varied, as did Kudoh (1988) , the
relatively weak influence of temporal variables was probably swamped by
the much larger effect of spacing in other studies. Interestingly,
roughness magnitude estimates are influenced more by changes in dot
spacing when they are along rather than across the scanning direction
(Connor and Johnson, 1992 ; Meftah and Chapman, 2000 ). This may be
caused by temporal effects, because stimulus temporal frequency is
affected when spacing varies along but not across scanning direction.
Ascertaining whether this explanation is valid requires modeling the
effect of frequency and spacing for dot patterns as Equation 3 does for gratings.
Roughness discrimination
The findings of this experiment verify that
Ft plays a role in perceived grating
roughness, in accord with its effects on afferent response rates. For
R-varying gratings this role is critical, whereas when
G varies, its effect tends to overwhelm that of
Ft. The contribution of temporal
factors that we found even during discrimination of
G-varying gratings is supported by the observation that
eliminating spatial cues, thereby inducing reliance on temporal cues,
can improve discrimination of fine gratings with high
Ft (Gamzu et al., 2000 ). Furthermore,
discrimination of dot spacing is better when it varies along rather
than across scanning direction (Lamb, 1983a ), consistent with
involvement of temporal factors and larger effects on roughness
magnitude estimates in the scanning direction (see above).
Possible neural coding mechanisms
Our study indicates that temporal and spatial factors interact to
evoke the percept of roughness. Although this study was not designed to
distinguish between potential neural coding mechanisms, some
interesting insights emerge.
Rate coding
One obvious candidate neural coding mechanism is peripheral
afferent discharge rate. This measure encodes G and
Ft (Eq. 3). The present study reveals
that both of these variables influence roughness in a manner that is
predictable from afferent firing rates. Across the conditions that we
studied, predicted SA afferent rates most consistently accounted for
observed roughness judgments. RA and PC afferent response rates matched
perceived roughness slightly better than SA rates in some conditions
but relatively poorly in other conditions. Thus, on the basis of linear
relationships between peripheral afferent rate and roughness ratings,
SAs seem most likely among afferent types to mediate roughness
perception. However, non-linear relationships were not examined, and it
is not clear to what extent inputs from different classes of peripheral afferents stay separate within the CNS (DiCarlo et al., 1998 ), so that
attributing a perceptual role to a specific afferent type is premature.
An argument against peripheral rate coding is that it is confounded by
nonspecific changes, e.g., in contact force, that can be produced even
by smooth surfaces. However, a concomitant temporal coding mechanism
(see below) could remove such confounds. There is ample empirical
support for rate coding. Grating roughness magnitude estimates
correlate well with SA and RA afferent response rates, all of which
increase with G and decrease with R under conditions of linear motion (Dorsch et al., 2000 ). This study is
consistent with Equation 3 and our findings. Both peripheral (Sathian
et al., 1989 ) and central (Sinclair and Burton, 1991a , 1993 ; Sinclair
et al., 1991 , 1996 ; Jiang et al., 1997 ; Pruett et al., 2000 )
somatosensory neurons increase their discharge rate with spacing,
paralleling the rise in perceived roughness with spacing. Although
afferent response rate did not vary consistently with R in a
previous investigation (Sathian et al., 1989 ), except for PCs, this may
have been caused by the use of sinusoidal motion, where the effect of
Ft could be obscured as it varies
continuously within a sweep. Finally, firing rates of RA and PC
afferents (Lamb, 1983b ) and primary somatosensory cortical neurons
(Sinclair and Burton, 1991b ) can account for the discriminability of
periodic surfaces differing in spacing.
Spatial coding
The degree of response rate variation among spatially distributed
members of the SA afferent pool correlates well with perceived roughness under various conditions (Connor et al., 1990 ; Connor and
Johnson, 1992 ; Blake et al., 1997 ; Dorsch et al., 2000 ). In theory,
such a spatial coding mechanism might be able to extract spatial
information from confounding temporal factors and use this spatial
information alone to compute roughness. Our findings definitively
refute this possibility. However, such a population spatial code could
well be sensitive to temporal, in addition to spatial, variables and
thus encode roughness changes depending on either element spacing or
Ft. This has not been tested experimentally.
Temporal coding
Both primary somatosensory afferents (Darian-Smith and Oke, 1980 ;
Morley and Goodwin, 1987 ; Goodwin et al., 1989 ) and central somatosensory neurons (Sinclair and Burton, 1991a ; Sinclair et al.,
1991 , 1996 ) represent grating Ft in
their firing patterns. Thus, the temporal variables important to
roughness judgments may be represented explicitly through a temporal
coding mechanism. Spatial variables might then be encoded independently
by a temporally insensitive mechanism, e.g., the ratio of RA to PC
afferent population response rates (Goodwin and Morley, 1987 ) or
possibly the degree of spatial variation in the SA afferent pool (see
above). As already pointed out, temporal coding could also complement a
rate code. The relevance of temporal coding in the somatosensory system
is underscored by the oscillatory behavior of certain somatosensory thalamic and cortical neurons (Ahissar et al., 1997 , 2000 ). Cortical neurons convey precise temporal information about vibrotactile stimuli
through a temporal code that is transformed into a rate code with
hierarchical progression (Pons et al., 1987 ; Burton et al., 1990 ) from
primary to secondary somatosensory cortex (Salinas et al., 2000 ).
Because the temporal characteristics of peripheral neural responses to
gratings and suprathreshold vibrotactile stimuli are similar (Goodwin
et al., 1989 ), a transformation from temporal to rate coding could also
operate for textured stimuli. Further neurophysiological investigation
is necessary to understand how the temporal information used in tactile
texture perception is encoded neurally, and whether one or more of the
above mechanisms are important.
 |
FOOTNOTES |
Received Jan. 8, 2001; revised April 16, 2001; accepted April 16, 2001.
This work was supported by National Institutes of Health Grant R29-NS
34111. We thank Andy Register and Harold Engler of the Georgia
Institute of Technology for designing and building the stimulator,
Harold Engler for its maintenance, Dale Rice (Department of Neurology,
Emory University) for machining support, and Hrishikesh Chakraborty
(Department of Biostatistics, Emory University) for help with
statistical analysis. We are indebted to Tony Goodwin for invaluable
discussion and to Jim DiCarlo and Ken Johnson for helpful comments.
Correspondence should be addressed to Dr. K. Sathian, Department of
Neurology, Emory University School of Medicine, WMRB-6000, Atlanta, GA
30322. E-mail: ksathia{at}emory.edu.
 |
REFERENCES |
-
Ahissar E,
Haidarliu S,
Zainos A
(1997)
Decoding temporally encoded sensory input by cortical oscillations and thalamic phase comparators.
Proc Natl Acad Sci USA
94:11633-11638[Abstract/Free Full Text].
-
Ahissar E,
Sosnik R,
Haidarliu S
(2000)
Transformation from temporal to rate coding in a somatosensory thalamocortical pathway.
Nature
406:302-306[Medline].
-
Blake DT,
Hsiao SS,
Johnson KO
(1997)
Neural coding mechanisms in tactile pattern recognition: the relative contributions of slowly and rapidly adapting mechanoreceptors to perceived roughness.
J Neurosci
17:7480-7489[Abstract/Free Full Text].
-
Burton H,
Sathian K,
Dian-Hua S
(1990)
Altered responses to cutaneous stimuli in the second somatosensory cortex following lesions of the postcentral gyrus in infant and juvenile macaques.
J Comp Neurol
291:395-414[Web of Science][Medline].
-
Cascio C,
Sathian K
(2000a)
Temporal frequency affects perceived tactile roughness.
Proc Cogn Neurosci Soc
117A:40.
-
Cascio C,
Sathian K
(2000b)
Contribution of temporal information to perceived tactile roughness.
Soc Neurosci Abstr
26:156.6.
-
Connor CE,
Johnson KO
(1992)
Neural coding of tactile texture: comparison of spatial and temporal mechanisms for roughness perception.
J Neurosci
12:3414-3426[Abstract].
-
Connor CE,
Hsiao SS,
Phillips JR,
Johnson KO
(1990)
Tactile roughness: neural codes that account for psychophysical magnitude estimates.
J Neurosci
10:3823-3836[Abstract].
-
Darian-Smith I,
Oke LE
(1980)
Peripheral neural representation of the spatial frequency of a grating moving across the monkey's finger pad.
J Physiol (Lond)
309:117-133[Abstract/Free Full Text].
-
DiCarlo JJ,
Johnson KO,
Hsiao SS
(1998)
Structure of receptive fields in area 3b of primary somatosensory cortex in the alert monkey.
J Neurosci
18:2626-2645[Abstract/Free Full Text].
-
Dorsch AK,
Yoshioka T,
Hsiao SS,
Johnson KO
(2000)
Peripheral neural mechanisms underlying roughness perception of fine stimulus patterns.
Soc Neurosci Abstr
26:156.3.
-
Gamzu E,
Barash S,
Ahissar E
(2000)
Improving tactile discrimination by eliminating spatial cues.
Soc Neurosci Abstr
26:547.25.
-
Goodwin AW,
Morley JW
(1987)
Sinusoidal movement of a grating across the monkey's fingerpad: representation of grating and movement features in afferent fiber responses.
J Neurosci
7:2168-2180[Abstract].
-
Goodwin AW,
John KT,
Sathian K,
Darian-Smith I
(1989)
Spatial and temporal factors determining afferent fiber responses to a grating moving sinusoidally over the monkey's fingerpad.
J Neurosci
9:1280-1293[Abstract].
-
Heller MA
(1989)
Texture perception in sighted and blind observers.
Percept Psychophys
45:49-54[Medline].
-
Hollins M,
Risner SR
(2000)
Evidence for the duplex theory of tactile texture perception.
Percept Psychophys
62:695-705[Medline].
-
Jiang W,
Tremblay F,
Chapman CE
(1997)
Neuronal encoding of texture changes in the primary and the secondary somatosensory cortical areas of monkeys during passive texture discrimination.
J Neurophysiol
77:1656-1662[Abstract/Free Full Text].
-
Johnson KO,
Hsiao SS
(1992)
Neural mechanisms of tactual form and texture perception.
Annu Rev Neurosci
15:227-250[Web of Science][Medline].
-
Johnson KO,
Hsiao SS,
Blake DT
(1996)
Linearity as the basic law of psychophysics: evidence from studies of the neural mechanisms of roughness magnitude estimation.
In: Somesthesis and the neurobiology of the somatosensory cortex (Franzen O,
Johansson R,
Terenius L,
eds), pp 213-228. Basel: Birkhauser Verlag.
-
Klatzky RL,
Lederman SJ,
Reed C
(1987)
There's more to touch than meets the eye: the salience of object attributes for haptics with and without vision.
J Exp Psychol Gen
116:356-369.
-
Krueger LE
(1970)
David Katz's Der Aufbau der Tastwelt (The world of touch): a synopsis.
Percept Psychophys
7:337-341.
-
Kudoh N
(1988)
Tactile perception of textured surfaces: effects of temporal frequency on perceived roughness by passive touch.
Tohoku Psychologica Folia
47:21-28.
-
Lamb GD
(1983a)
Tactile discrimination of textured surfaces: psychophysical performance measurements in humans.
J Physiol (Lond)
338:551-565[Abstract/Free Full Text].
-
Lamb GD
(1983b)
Tactile discrimination of textured surfaces: peripheral neural coding in the monkey.
J Physiol (Lond)
338:567-587[Abstract/Free Full Text].
-
Lederman SJ
(1974)
Tactile roughness of grooved surfaces: the touching process and effects of macro- and microsurface structure.
Percept Psychophys
16:385-395[Web of Science].
-
Lederman SJ
(1981)
The perception of surface roughness by active and passive touch.
Bull Psychonomic Soc
18:253-255.
-
Lederman SJ,
Klatzky RL
(1987)
Hand movements: a window into haptic object recognition.
Cognit Psychol
19:342-368[Web of Science][Medline].
-
Lederman SJ,
Taylor MM
(1972)
Fingertip force, surface geometry and the perception of roughness by active touch.
Percept Psychophys
12:401-408.
-
Lederman SJ,
Loomis JM,
Williams DA
(1982)
The role of vibration in the tactual perception of roughness.
Percept Psychophys
32:109-116[Web of Science][Medline].
-
Levitt H
(1971)
Transformed up-down methods in psychoacoustics.
J Acoust Soc Am
49:467-477.
-
Meenes M,
Zigler MJ
(1923)
An experimental study of the perceptions roughness and smoothness.
Am J Psychol
34:542-549.
-
Meftah EM,
Chapman CE
(2000)
Relative effects of the spatial and temporal characteristics of scanned surfaces on human perception of tactile roughness using passive touch.
Exp Brain Res
132:351-361[Web of Science][Medline].
-
Morley JW,
Goodwin AW
(1987)
Sinusoidal movement of a grating across the monkey's fingerpad: temporal patterns of afferent fiber responses.
J Neurosci
7:2181-2191[Abstract].
-
Morley JW,
Goodwin AW,
Darian-Smith I
(1983)
Tactile discrimination of gratings.
Exp Brain Res
49:291-299[Web of Science][Medline].
-
Pons TP,
Garraghty PE,
Friedman DP,
Mishkin M
(1987)
Physiological evidence for serial processing in somatosensory cortex.
Science
237:417-420[Abstract/Free Full Text].
-
Pruett JRJ,
Sinclair RJ,
Burton H
(2000)
Response patterns in second somatosensory cortex (SII) of awake monkeys to passively applied tactile gratings.
J Neurophysiol
84:780-797[Abstract/Free Full Text].
-
Salinas E,
Hernandez A,
Zainos A,
Romo R
(2000)
Periodicity and firing rate as candidate neural codes for the frequency of vibrotactile stimuli.
J Neurosci
20:5503-5515[Abstract/Free Full Text].
-
Sathian K
(1987)
Tactile perception of texture: representation of gratings in the peripheral afferent discharge.
In: PhD thesis The University of Melbourne.
-
Sathian K
(1989)
Tactile sensing of surface features.
Trends Neurosci
12:513-519[Medline].
-
Sathian K,
Burton H
(1991)
The role of spatially selective attention in the tactile perception of texture.
Percept Psychophys
50:237-248[Web of Science][Medline].
-
Sathian K,
Zangaladze A
(1997)
Tactile learning is task-specific but transfers between fingers.
Percept Psychophys
59:119-128[Web of Science][Medline].
-
Sathian K,
Goodwin AW,
John KT,
Darian-Smith I
(1989)
Perceived roughness of a grating: correlation with responses of mechanoreceptive afferents innervating the monkey's fingerpad.
J Neurosci
9:1273-1279[Abstract].
-
Sinclair RJ,
Burton H
(1991a)
Neuronal activity in the primary somatosensory cortex in monkeys (Macaca mulatta) during active touch of textured surface gratings: responses to groove width, applied force, and velocity of motion.
J Neurophysiol
66:153-169[Abstract/Free Full Text].
-
Sinclair RJ,
Burton H
(1991b)
Tactile discrimination of gratings: psychophysical and neural correlates in human and monkey.
Somatosens Mot Res
8:241-248[Web of Science][Medline].
-
Sinclair RJ,
Burton H
(1993)
Neuronal activity in the second somatosensory cortex of monkeys (Macaca mulatta) during active touch of gratings.
J Neurophysiol
70:331-350[Abstract/Free Full Text].
-
Sinclair RJ,
Pruett JR,
Burton H
(1996)
Responses in primary somatosensory cortex of rhesus monkey to controlled application of embossed grating and bar patterns.
Somatosens Mot Res
13:287-306[Web of Science][Medline].
-
Sinclair RJ,
Sathian K,
Burton H
(1991)
Neuronal responses in ventroposterolateral nucleus of thalamus in monkeys (Macaca mulatta) during active touch of gratings.
Somatosens Mot Res
8:293-300[Medline].
-
Srinivasan MA,
Whitehouse JM,
LaMotte RH
(1990)
Tactile detection of slip: surface microgeometry and peripheral neural codes.
J Neurophysiol
63:1323-1332[Abstract/Free Full Text].
Copyright © 2001 Society for Neuroscience 0270-6474/01/21145289-08$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
S. J. Lederman and R. L. Klatzky
Haptic perception: A tutorial
Atten Percept Psychophys,
October 1, 2009;
71(7):
1439 - 1459.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
G. E. LEGGE, C. MADISON, B. N. VAUGHN, A. M. Y. CHEONG, and J. C. MILLER
Retention of high tactile acuity throughout the life span in blindness
Atten Percept Psychophys,
November 1, 2008;
70(8):
1471 - 1488.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Depeault, E.-M. Meftah, and C. E. Chapman
Tactile Speed Scaling: Contributions of Time and Space
J Neurophysiol,
March 1, 2008;
99(3):
1422 - 1434.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Hollins, F. Lorenz, and D. Harper
Somatosensory coding of roughness: the effect of texture adaptation in direct and indirect touch.
J. Neurosci.,
May 17, 2006;
26(20):
5582 - 5588.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Gamzu and E. Ahissar
Importance of Temporal Cues for Tactile Spatial- Frequency Discrimination
J. Neurosci.,
September 15, 2001;
21(18):
7416 - 7427.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|