The effect of skin temperature on vibrotactile sensitivity

The effect of skin temperature on detection of vibrotactile stimuli was measured for vibrations of 30 and 250 Hz. Data for the 250-Hz stimulus supported the results of Weitz (1941), who found that thresholds for 100-, 256-, and 900-Hz vibration varied as a If-shape function of skin temperature with a minimum at about 37°C. Temperature had a negligible effect on sensitivity at 30 Hz. A second experiment examined a range of frequencies between 30 and 250 Hz. Cooling greatly lowered sensitivity only to 150- and 250-Hz stimuli. Warming reduced sensitivity less, but more uniformly across frequencies. It was concluded that cooling may affect vibrotactile thresholds by decreasing the sensitivity of Pacinian corpuscles; the reason for the decrease in sensitivity due to warming is unclear.     

Effects of the menstrual cycle on vibrotactile sensitivity

Psychophysical thresholds for the detection of vibration delivered to the thenar eminence of the right hands of young males and females were measured every other day for 30–34 days. The frequency of the vibratory stimulus was either 15 or 250 Hz. The sinusoidal stimuli applied through a 3.0-cm² contactor were 700 msec in duration and had rise-fall times of 25 msec. Stimulus amplitude was measured with a calibrated accelerometer mounted on the moving element of the vibrator. Data were plotted as a function of successive days in the menstrual cycle. Thresholds for detecting the 15-Hz stimulus did not change significantly, whereas thresholds for detecting the 250-Hz stimulus varied significantly over the menstrual cycle. The 250-Hz threshold became progressively lower as subjects approached the onset of menstruation. After the onset of menstruation, the 250-Hz threshold gradually increased, reaching a maximum value approximately 12 or 13 days later. Soon after the 12th or 13th day of the cycle, the threshold again began to decline and continued to decline until the onset of the next menstrual cycle. The thresholds of women taking birth control pills did not change systematically over the testing period.     

The effect of location on the discrimination of spatial vibrotactile patterns

The present study examined whether the locations of patterns on the skin affected the ability to process information about their shapes. In Experiment 1, pairs of spatial vibrotactile patterns, using the array from the Optacon, were presented sequentially to subjects’ left index fingerpads. The location of each pattern in a pair was varied randomly among four locations on the skin. The subjects responded “same” or “different” on the basis of the shapes of patterns, regardless of their locations. Discrimination accuracy was highest and response time fastest when patterns occupied identical locations (ILs), and performance suffered with increasing distance between patterns. In Experiment 2, pairs were presented to corresponding points or to noncorresponding points on separate fingerpads. When patterns occupied corresponding points on separate fingers, accuracy was lower than when patterns occupied ILs on a single finger, but higher than when patterns occupied noncorresponding points on separate fingers. The results suggested that discriminability declined partly because patterns did not occupy ILs, and partly because separate locations had different densities of innervation.     

Sensation magnitude scales for vibrotactile stimulation of the tongue and thenar eminence

This study represents the first attempt to generate magnitude-estimation and magnitude-balance functions for the human tongue. Vibrotactile magnitude scales for the tongue and thenar eminence of the hand were investigated for nine adult subjects. The methods of magnitude estimation and magnitude production were used to obtain magnitude-balance functions for both structures. The magnitude-estimation task resulted in magnitude functions for the tongue which were similar in slope value to those found for the thenar eminence. The magnitude-production task also gave magnitude functions which were similar in slope value for the two structures.     

The effect of vertical tongue loading on the position perception of the tongue

We investigated the effects of vertical tongue loading on the position perception of the tongue. Five male and 5 female university students served as subjects. Vertical upward and downward loading forces were applied to the tongue of the subjects. Their task was to judge the perceived horizontal position of the tongue after tongue-loading directions. The means of the judgments for the control conditions (no tongue loading) were compared with the judgments for perceived horizontal position after tongue loading. The results showed that vertical tongue loading produced a shift in the perceived horizontal direction opposite to the applied force. These results fully replicated the analogous aftereffect found by Grover and Craske (1991) for horizontal tongue loading. However, the judgments of perceived horizontal position in the present study had lower variability than did those in Grover and Craske's study, suggesting that mapping of the tongue along the vertical axis is more precise than mapping along the horizontal axis.     

The initial effect of noise on a simple vibrotactile learning task

In two experiments the effect of loud noise on a simple vibrotactile learning task was studied. After learning the task to criterion, 10 male and 10 female Ss received two pairs of test trials, one without noise, and one in continuous noise (a 1,000 cps pure tone at 90 dB SPL). An additional 10 male and 10 female Ss learned the same task and also received the same two pairs of test trials, but instead of receiving continuous noise for the second condition, they received an intermittent noise (random numbers presented at 2 sec intervals at 95 dB SPL). In the first experiment noise had a significant effect on the performance of the 20-subject group and also on the females in the group. Noise did not significantly affect the performance of males. In the second experiment noise had no significant effect on either males or females.     

Touch noise increases vibrotactile sensitivity in old and young

Stochastic resonance (SR) occurs when the detection of a subthreshold signal is aided by the presence of random energy fluctuations in the signal modality, commonly called noise. SR is counterintuitive because such noise usually worsens performance. Nonetheless, SR has been demonstrated both theoretically and experimentally in human sensory systems. Using a psychophysically sophisticated paradigm, we show that SR aids the detection of vibrating touch stimuli presented to the foot soles of both healthy elderly people with elevated vibrotactile thresholds and healthy young people with normal vibrotactile thresholds. The results also suggest that it is possible to know a priori the amount of noise needed for optimal SR effects given the degree to which the signal is subthreshold. Thus, SR may be practical as a rehabilitative aid for individuals with elevated sensory thresholds.     

The effect of shape and location on temporal masking of spatial vibrotactile patterns

Target patterns presented to uncued locations on a single fingerpad were followed by either same-shape (SS) maskers or different-shape (DS) maskers presented to either the same location (SLoc) or a different location (DLoc). DS maskers interfered with identification more when they were at SLoc than when they were at Dloc, but the reverse was true for SS maskers; they interfered more at DLoc than at SLoc. When targets were presented to cued locations, performance in the absence of maskers improved, but the pattern of interference from maskers resembled that for uncued presentation. The proportion of masker responses on incorrect trials revealed that both temporal masking and response competition may be involved in the effects of location on pattern identification.     

The effect of loading on position sense in the tongue

The position sense of the tongue and aftereffects on the position sense subsequent to loading were directly investigated. Nine subjects judged the straightahead with the tongue before and after straining laterally with the tongue against the horizontal force induced by a 29.5-g weight. Two of these subjects also participated in the experiment after the surface of the tongue had been anesthetized. Prior loading of the tongue biased the subjects' subsequent judgment of the straight-ahead; following loading, the tongue was placed farther in the direction of the previous effort. The results are discussed with reference to postcontraction effects from experiments on loading the limb and eye.     

Lingual vibrotactile screening: an investigation of normal sensitivity based on multiple threshold determinations

This report describes a standardized training and sensory screening procedure which was used to obtain 7 separate lingual vibrotactile thresholds for each of 5 normal subjects during a 30-day interval. Baseline observations of lingual sensitivity were highly consistent and occurred within a narrow range of contractor displacements. The authors conclude that the screening method provides a quick and reliable clinical tool for general diagnostic use and discuss directions for continued research applications.     

The shape of the vibrotactile loudness function: The effect of stimulus repetition and skin-contactor coupling

In the psychophysical literature describing the relationships between physical and psychological magnitudes, as physical intensity increases, perceived intensity often grows much faster near threshold than at higher levels. In this laboratory, however, the loudness curve for sinusoidal vibrotactile stimuli was best fit by a single-limbed function rather than by the expected two-limbed function. In the present study, we measured the growth of vibrotactile loudness of 250-Hz sinusoidal stimuli by the method of absolute magnitude estimation to explore the source of the one- versus two-limbed discrepancy. The number of times that the stimulus was presented was varied, as well as whether the stimulator contacted the skin with constant force or constant penetration. Neither of these manipulations affected the shape of the loudness function consistently. Number of repetitions influenced the shapes of the magnitude estimation functions, but only for a few individuals. Skin-contactor coupling did not affect the shapes of the functions, although the absolute level (vibrotactile loudness) was consistently greater for constant indentation.     

The effects of complexity on the perception of vibrotactile patterns

Vibrotactile patterns were presented to subjects’ left index fmgerpads using the array from the Optacon. A set of simple (one-line) patterns and a set of complex (two-line) patterns were constructed so that they were equally identifiable when presented individually. In Experiment 1, discrimination performance was lower for two-line patterns than for one-line patterns. Communality, the number of lines that two patterns share in common, appeared to be the major factor in reducing discrimination performance for two-line patterns. Experiment 2 measured the time required to identify individual patterns. There was no significant difference in identification times for one- and two-line patterns, suggesting that features within a pattern were processed simultaneously. In the presence of a temporal masking stimulus (Experiment 3), two-line patterns were more difficult to identify than one-line patterns, but reaction times were similar for the two sets of patterns. The results suggest that varying complexity affects perception of patterns at later stages of processing.     

Exposure effects on the psychophysical scaling methods of magnitude estimation and cross-modal matching for vibrotactile stimulation of the tongue and hand

The purpose of the present study was to investigate possible effects of exposure upon psychophysical scaling responses when vibrotactile magnitude estimation and cross-modal matching are conducted within the same experiment. Four groups of 10 subjects each, with an over-all age range of 18-23 yr., were employed. Groups 1 and 2 performed magnitude estimation for lingual vibrotaction and cross-modal matching with the lingual vibrotactile stimulus as the standard. Group 1 received the magnitude-estimation task first and Group 2 received the cross-modal-matching task first. Groups 3 and 4 performed magnitude estimation for vibrotaction applied to the thenar eminence of the hand and cross-modal matching with the vibrotactile stimulus applied to the thenar eminence of the hand as the standard. Group 3 received the magnitude-estimation task first and Group 4 received the cross-modal-matching task first. The psychophysical scaling methods of magnitude estimation and cross-modal matching showed very little exposure effect of one upon the other when used in the same experiment. Also, magnitude scaling responses tended to increase more rapidly with increases in vibrotactile stimulus intensity when the test site was the thenar eminence of the hand as opposed to the dorsum of the tongue.     

Midline and off-midline tongue and right- and left-hand vibrotactile thresholds of stutterers and normal-speaking individuals

Vibrotactile thresholds for 7 male stutterers and 7 normal-speaking men (age range for both groups = 19 to 32 yr.) were obtained from the right, midline, and left sides of the lingual dorsum, and the thenar eminences of both hands. The stutterers showed slightly higher (less sensitive) mean thresholds than the normal speakers for all three lingual test sites. This was not the case for the thresholds obtained from both hands. The preliminary data suggest that oral peripheral sensory integrity might be somewhat different for stutterers than for normal-speaking individuals.     

The effects of complexity on the perception of vibrotactile patterns.

Vibrotactile patterns were presented to subjects' left index fingerpads using the array from the Optacon. A set of simple (one-line) patterns and a set of complex (two-line) patterns were constructed so that they were equally identifiable when presented individually. In Experiment 1, discrimination performance was lower for two-line patterns than for one-line patterns. Communality, the number of lines that two patterns share in common, appeared to be the major factor in reducing discrimination performance for two-line patterns. Experiment 2 measured the time required to identify individual patterns. There was no significant difference in identification times for one- and two-line patterns, suggesting that features within a pattern were processed simultaneously. In the presence of a temporal masking stimulus (Experiment 3), two-line patterns were more difficult to identify than one-line patterns, but reaction times were similar for the two sets of patterns. The results suggest that varying complexity affects perception of patterns at later stages of processing.     

The effect of language on visual contrast sensitivity

Embodied cognition and perceptual symbol theories assume that higher cognition interacts with and is grounded in perception and action. Recent experiments have shown that language processing interacts with perceptual processing in various ways, indicating that linguistic representations have a strong perceptual character. In the present study, we have used signal detection theory to investigate whether the comprehension of written sentences, implying either horizontal or vertical orientation, could improve the participants' visual sensitivity for discriminating between horizontal or vertical square-wave gratings and noise. We tested this prediction by conducting one main and one follow-up experiment. Our results indicate that language can, indeed, affect perception at such a low level of the visual process and thus provide further support for the embodied theories of cognition.     

Absolute localization of vibrotactile stimuli on the torso

Vibrotactile mobility systems present spatial information such as the direction of a waypoint through a localized vibration on the torso. Using these systems requires the ability to determine the absolute location of the stimulus. Because data are available only on the ability to determine the relative location of stimuli on the torso, we developed a novel method for measuring absolute localization on the basis of triangulation. For 15 observers, we calculated the subjective location of visual and tactile stimuli on the frontal half of the torso. The size of the 95% confidence intervals around the subjective tactile locations is about the size of the stimuli (1.66 cm) and is slightly larger than that around the subjective visual locations (mean difference, 0.17 cm). The error in tactile judgments over and above that in the visual judgments is present only for locations near the body midline. When the subjective visual and tactile locations are not co-located, the difference can best be described by a shift along the radius from the body midaxis. The same holds for the differences between the veridical and the subjective locations. Therefore, the difference between the veridical and the subjective directions of a stimulus is small. The results make us believe that stimulus locations on the torso are coded in polar coordinates of which the angle is perceptual invariant and the distance is less important, probably because it varies with changes in, among other things, posture and breathing.     

The effect of various heteromodal stimuli on visual sensitivity

Ten experiments are reported. In each the effect of a heteromodal stimulus on visual sensitivity is investigated. With one exception all the stimuli produced a small increase in visual sensitivity. A number of possible explanations of intersensory facilitation are considered.