THE INFLUENCE OF AUDITORY STIMULUS INTENSITY ON APPARENT DURATION

B erglund , B., B erglund , U., E kman , G. & F rankenhaeuser , M. The influence of auditory stimulus intensity on apparent duration. Scand J. Psychol ., 1969, 10 21–26.— apparent duration of an auditory signal of 1000 C/S was measured by the method of magnitude estimation. Ten different stimulus intensities ranging from 57 to 104 dB were used in combination with three different durations: 50, 250, and 500 msec. The results showed that the apparent duration of the signal grew as a logarithmic function of stimulus intensity. These results are consistent with the hypothesis relating apparent duration to activation level as well as with results of similar experiments involving electrical and vibrotactile stimulation.     

Contralateral enhancement and suppression of vibrotactile sensation

A psychophysical matching procedure was used to measure the effect of a conditioning stimulus on the vibrotactile sensation magnitude of a test stimulus. When both stimuli were applied to the thenar eminence of the same hand, the conditioning stimulus enhanced the sensation magnitude of the test stimulus. Enhancement was also observed when the test stimulus was on the thenar eminence and the conditioning stimulus was either on the contralateral thenar eminence, the ipsilateral middle finger, or the contralateral middle finger. When the conditioning and test stimuli were applied to separate sites, enhancement was maximal when At between the stimuli was 150 msec. At Ate less than 100 msec, suppression was observed. Enhancement and suppression were observed only when the frequencies of the two stimuli were within the same vibrotactile information processing channel.     

Similarity of tactual and visual picture recognition with limited field of view.

Subjects attempted to recognize simple line drawings of common objects using either touch or vision. In the touch condition, subjects explored raised line drawings using the distal pad of the index finger or the distal pads both of the index and of the middle fingers. In the visual condition, a computer-driven display was used to simulate tactual exploration. By moving an electronic pen over a digitizing tablet, the subject could explore a line drawing stored in memory; on the display screen a portion of the drawing appeared to move behind a stationary aperture, in concert with the movement of the pen. This aperture was varied in width, thus simulating the use of one or two fingers. In terms of average recognition accuracy and average response latency, recognition performance was virtually the same in the one-finger touch condition and the simulated one-finger vision condition. Visual recognition performance improved considerably when the visual field size was doubled (simulating two fingers), but tactual performance showed little improvement, suggesting that the effective tactual field of view for this task is approximately equal to one finger pad. This latter result agrees with other reports in the literature indicating that integration of two-dimensional pattern information extending over multiple fingers on the same hand is quite poor. The near equivalence of tactual picture perception and narrow-field vision suggests that the difficulties of tactual picture recognition must be largely due to the narrowness of the effective field of view.     

Effect of display movement on tactile pattern perception

The effect of display movement on the ability of subjects to rec ognize alphabetic shapes tactually was investigated. The display consisted of a computer-controlled 8-by-6 array of small airjet stimulators that could be physically translated in a small circle by means of a mechanical linkage. The experimental parameters were the stimulus duration, the angular velocity of the display, and the amplitude of the rotation. Recognition accuracy increased with stimulus duration between 100 and 400 msec. For a rotation amplitude of 0.8 cm, a maximum in recognition accuracy occurred at a rotation velocity of 400 rpm, or 150 msec. per revolution. The optimum angular velocity appeared to decrease as the amplitude of rotation increased. From these results and certain related neurophysiological evidence, a hypothetical model is suggested which qualitatively can account for the data.     

Effect of display movement on tactile pattern perception

The effect of display movement on the ability of subjects to recognize alphabetic shapes tactually was investigated. The display consisted of a computer-controlled 8-by-6 array of small airjet stimulators that could be physically translated in a small circle by means of a mechanical linkage. The experimental parameters were the stimulus duration, the angular velocity of the display, and the amplitude of the rotation. Recognition accuracy increased with stimulus duration between 100 and 400 msec. For a rotation amplitude of 0.8 cm, a maximum in recognition accuracy occurred at a rotation velocity of 400 rpm, or 150 msec. per revolution. The optimum angular velocity appeared to decrease as the amplitude of rotation increased. From these results and certain related neurophysiological evidence, a hypothetical model is suggested which qualitatively can account for the data.     

Immediate and delayed recognition of sequentially presented random shapes.

Two experiments tested whether short-term memory accounts for the recency effect observed with rapid sequential presentation of nonverbal stimuli. Four random shapes were presented sequentially (with no interstimulus interval) on each trial at rates of 150 msec, 250 msec, 500 msec, and 1,000 msec per stimulus. Subsequent recognition varied positively with exposure duration, ranging from 57% at 150 msec to 77% at 1,000 msec. Two serial position effects were observed: a slight decrease in recognition accuracy for the first stimulus in each sequence and a large increase in recognition for the last stimulus in each sequence. The recency effect was not altered by an intervening 30-sec delay, an intervening 30-sec copying task, or an intervening 30-sec copying and counting task. Since neither visual nor verbal distractors altered recognition accuracy, it was suggested that all shapes were processed directly into long-term memory storage. It also was hypothesized that long-term storage of a nonverbal stimulus requires identification of a distinctive feature of the stimulus and that this process may continue for a brief period after actual stimulus offset.     

Short-term visual storage

The delay between the offset of a briefly exposed array of letters and digits and the onset of an arrow pointing at one of the array positions was varied from 0 to 5000 msec. In addition, the luminance of the stimulus array was varied over three levels. The Ss reported the item in the position indicated by the arrow. Luminance, delay, and the luminance by delay interaction were all significant I Performance monotonically decreased from a delay of 0 msec to a delay of 250 msec, but the percent correct remained fairly constant from 250 msec to 5000 msec. With delays shorter than 250 msec, high luminance arrays showed better performance.     

Vibrotactual choice reaction time,tactile receptor systems and ideomotor compatibility

In most of the literature on human performance the results of an experiment by Leonard (1959) are quoted as the most outstanding example of perfect S-R-compatibility. In that experiment the fingertips were stimulated by a 50 Hz vibration; the vibrating armature had to be depressed and the reaction times of the right index finger were recorded. The reaction time was found not to increase with an increasing number of tactual choices. In experiment 1 of the present study, also applying 50 Hz vibrations, the reaction times of other fingers were also reported. In addition the response stimulus interval (RSI) was varied. Leonard's results were not replicated: reaction time increased with the number of tactual choices at all levels of RSI. In experiment 2 the frequency and amplitude of vibration were systematically varied and it turned out that these variables could account for the differences between the results found. An increase in reaction time with the number of tactual choices was found with weak vibrations, but not with strong vibrations. The differences in reaction time patterns appeared to be caused by differences in tactile receptor systems (i.e. the non-Pacini versus the Pacinian system). It was concluded that the concept of S-R-compatibility did not cover the pattern of results but that the concept of ideomotor compatibility did.     

Illusory recouplings of onsets and terminations of glide tone components

We present a new auditory illusion, the gap transfer illusion, supported by phenomenological and psychophysical data. In a typical situation, an ascending frequency glide of 2,500 msec with a temporal gap of 100 msec in the middle and a continuously descending frequency glide of 500 msec cross each other at their central positions. These glides move at the same constant speed in logarithmic frequency in opposite directions. The temporal gap in the long glide is perceived as if it were in the short glide. The same kind of subjective transfer of a temporal gap can take place also when the stimulus pattern is reversed in time. This phenomenon suggests that onsets and terminations of glide components behave as if they were independent perceptual elements. We also find that when two long frequency glides are presented successively with a short temporal overlap, a long glide tone covering the whole duration of the pattern and a short tone around the temporal middle can be perceived. To account for these results, we propose an event construction model, in which perceptual onsets and terminations are coupled to construct auditory events and the proximity principle connects these elements.     

Visual information processing of sequentially presented inputs: I. effects of input timing on sub-span storage and retrieval mechanisms’

A computer-based cathode-ray tube display system was employed to study the effect of subspan list length, i.e., two, three, or four five-letter words, and several interstimulus interval (ISI) values, i.e., 100, 150, 200, 250, 300, 500, and 700 msec, on visual information processing. Complicated interactions were found between list length and IS1 values. Two classes of Ss were identified and labeled as “slow” and “fast” processors and the overall findings were related to a provisional model of visual information processing with sequential inputs.     

Involuntary attentional shifts due to orientation differences

We tested the ability of orientation differences to cause involuntary shifts of visual attention and found that these attentional shifts can occur in response to an orientation “pop-out” display. Texturelike cue stimuli consisting of discrete oriented bars, with either uniform orientation or containing a noninformative orthogonally oriented bar, were presented for a variable duration. Subsequent to or partially coincident with the cue stimulus was the target display of a localization or two-interval forced-choice task, followed by a mask display. Naive subjects consistently showed greater accuracy in trials with the target at the location of the orthogonal orientation compared with trials with uniformly oriented bars, with only 100 msec between the cue and mask onsets. Discriminating these orientations required a stimulus onset asynchrony (SOA) of 50–70 msec. The attentional facilitation is transient, in most cases absent, with a cue-mask SOA of 250 msec. These results suggest that the preattentive character of some texture discrimination tasks with SOAs of only 100 msec is vitiated by the involuntary attentional shifts that are caused by orientation differences.     

Automatic and Strategic Retrieval of Structure Knowledge Following Two Modes of Learning

This study tested the hypothesis that strategic and non-strategic learning result in knowledge representations that are distinguished by different modes of retrieval for information about constituent structure. Subjects were taught concepts under conditions designed to induce either a strategic or non-strategic mode of learning. Following training, subjects participated in an attribute priming task designed to assess the extent to which information about constituent structure was automatically or strategically activated when concept knowledge was retrieved. Activation was measured at three SOAs: 250 msec, 500 msec, and 2000 msec. For the strategically learned concept, information about constituent structure did not show evidence of activation until 2000 msec. For the non-strategically learned concept this information was activated by 250 msec but had declined to baseline by 2000 msec. These findings suggest that information about constituent structure is available for retrieval by strategic processes following strategic learning, but that this information is not available for retrieval by strategic processes following non-strategic learning. It is, however, available for automatic retrieval following non-strategic learning.     

Timing in trace conditioning of the nictitating membrane response of the rabbit (Oryctolagus cuniculus): scalar, nonscalar, and adaptive features

Using interstimulus intervals (ISIs) of 125, 250, and 500 msec in trace conditioning of the rabbit nictitating membrane response, the offset times and durations of conditioned responses (CRs) were collected along with onset and peak latencies. All measures were proportional to the ISI, but only onset and peak latencies conformed to the criterion for scalar timing. Regarding the CR's possible protective overlap of the unconditioned stimulus (US), CR duration increased with ISI, while the peak's alignment with the US declined. Implications for models of timing and CR adaptiveness are discussed.     

Display polarity, stimulus exposure duration, and visual lobe shape

This study investigated the effects of visual display polarity and stimulus exposure duration on visual lobe shape. Analysis showed that regardless of display polarity and exposure duration combinations tested here, visual lobe contours were slightly irregular and asymmetric, of medium roundness, with a moderately rough boundary, and horizontally elongated with a mean length-width ratio of 1.53. Visual lobes mapped with negative display polarity were significantly rounder, slightly more regular and more symmetric along the vertical axis, compared with those mapped with positive polarity. Under the different polarity conditions, there were no significant differences in visual lobe area, perimeter, boundary smoothness, and elongation. When stimulus exposure duration increased from 200 to 400 msec. and from 200 to 300 msec., there were significant increases in the visual lobe area, perimeter, roundness, boundary smoothness, and regularity. No such changes were found when duration increased from 300 to 400 msec. Exposure durations did not have a significant effect on the shape categories of elongation and horizontal symmetry for the different stimuli. There were no statistically significant interactions between polarity and stimulus exposure duration for any of the lobe shape indexes used here.     

Enhancement and summation in the perception of two successive vibrotactile stimuli

Enhancement and summation were found to be fundamentally different perceptual processes affecting the sensation magnitude of two successive vibrotactile stimuli. Enhancement, defined operationally as an increment in the subjective magnitude of one stimulus due to the presentation of a prior stimulus, and summation, defined as an increment in overall subjective magnitude of the two stimuli, were measured for sinusoidal vibration of the thenar eminence of the hand. The effect of summation was maximum when the two stimuli greatly differed in frequency, whereas maximum enhancement effects were found when both stimuli were close in frequency. The summation effect showed little decay as the interstimulus interval was increased to as much as 500 msec, whereas enhancement effects decayed to zero at approximately 500 msec. Results were similar to those obtained in comparable studies of audition and support the hypothesis that there are at least two distinct information-processing channels for the perception of cutaneous vibration.     

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.     

Memory search and visual spatial attention: An event-related brain potential analysis

Event-related brain potentials (ERPs) were recorded from subjects as they attended to one diagonal of a visual display. The task was to respond only to memory set items (targets) at the attended diagonal and to ignore stimuli at the other diagonal. The probability that the display contained either an attended or an unattended target was 0.30. The spatial separation between attended and unattended stimuli was 1.6°. The ERP elicited by stimuli at the unattended diagonal contained a sequence of phasic components. The early N₁₇₀ and P₂₅₀ components were elicited by the onset of the display and the later components N₄₈₀ and P₅₅₀ by the offset of the display. The presence of masks delayed N₁₇₀ and P₂₅₀. The ERPs elicited by attended non-targets, in addition, contained an increased N₃₅₀ (C_z, F_z) and P₄₁₀ (P_3a, P_z, C_z). The ERPs elicited by attended and unattended non-targets started to differ after 200 msec. This finding suggested that selection is relatively late if selection must be based on a conjunction of features (location and orientation) and if the spatial separation between attended and unattended stimuli is small. Memory-set size affected the ERPs after 250 msec. The ERPs elicited by attended stimuli contained a broadly distributed (F_z, C_z, P_z) negative endogeneous component. The amplitude of this component was related to memory-set size. Finally, the ERPs elicited by attended targets contained a large P_3b (P_z, O_z) with a peak latency around 600 msec. The ERP results suggested the existence of three processing stages: (1) orienting to the attended stimuli; (2) controlled search, and (3) target decision.     

Duration discrimination of empty and filled intervals marked by auditory and visual signals

Experiments 1 and 2 compared, with a single-stimulus procedure, the discrimination of filled and empty intervals in both auditory and visual modalities. In Experiment 1, in which intervals were about 250 msec, the discrimination was superior with empty intervals in both modalities. In Experiment 2, with intervals lasting about 50 msec, empty intervals showed superior performance with visual signals only. In Experiment 3, for the auditory modality at 250 msec, the discrimination was easier with empty intervals than with filled intervals with both the forced-choice (FC) and the single stimulus (SS) modes of presentation, and the discrimination was easier with the FC than with the SS method. Experiment 4, however, showed that at 50 and 250 msec, with a FC-adaptive procedure, there were no differences between filled and empty intervals in the auditory mode; the differences observed with the visual mode in Experiments 1 and 2 remained significant. Finally, Experiment 5 compared differential thresholds for four marker-type conditions, filled and empty intervals in the auditory and visual modes, for durations ranging from .125 to 4 sec. The results showed (1) that the differential threshold differences among marker types are important for short durations but decrease with longer durations, and (2) that a generalized Weber’s law generally holds for these conditions. The results as a whole are discussed in terms of timing mechanisms.     

Lack of evidence for a tactual Poggendorff illusion

Lucca, Dellantonio, and Riggio (1986) reported large distortions in a tactual analogue of the visual Poggendorff illusion. They also reported large effects in the direction opposite to the visual illusion, which they termed "inversions." However, their evidence for such effects is questionable; they used what we consider to be inappropriate measurement and analysis procedures. In attempting to replicate their experiment, and in conducting four additional experiments, we found no evidence at all for their alleged tactual analogue of the visual Poggendorff effect. Instead, we demonstrated that "inversions" are likely due to the use of a raised stimulus display that causes artifactual mistracking, which is totally unrelated to normal mechanisms of alignment judgment. We also discuss the possible role of intersensory factors in the generation of tactual illusions.     

Symmetry in haptic and in visual shape perception

Four experiments tested the hypothesis that bilateral symmetry is an incidental encoding property in vision, but can also be elicited as an incidental effect in touch, provided that sufficient spatial reference information is available initially for haptic inputs to be organized spatially. Experiment 1 showed that symmetry facilitated processing in vision, even though the task required judgments of stimulus closure rather than the detection of symmetry. The same task and stimuli failed to show symmetry effects in tactual scanning by one finger (Experiment 2). Experiment 3 found facilitating effects for vertically symmetric open stimuli, although not for closed patterns, in two-forefinger exploration when the fore-fingers had previously been aligned to the body midaxis to provide body-centered spatial reference. The one-finger exploration condition again failed to show symmetry effects. Experiment 4 replicated the facilitating effects of symmetry for open symmetric shapes in tactual exploration by the two (previously aligned) forefingers. Closed shapes again showed no effect. Spatial-reference information, finger movements, and stimulus factors in shape perception by touch are discussed.