The effect of masker duration on forward and backward masking

Temporal masking of clicks by noise was investigated using forward and backward masking paradigms. Both the noise duration and the temporal separation, ΔT, between the click and noise were varied. For very brief ΔTs (100 microsec) and for very long ΔTs (100 msec), the duration of the masker did not greatly affect the click threshold. However, for intermediate ΔTs (3 msec), the threshold increased by as much as 44 dB as the noise duration increased from 0.1 to 100 msec. Temporal weighting functions, which describe the relative effectiveness of the noise as a function of ΔT, were computed from these data.     

Temporal discrimination as a function of marker duration

In a series of three experiments, the effect of marker duration on temporal discrimination was evaluated with empty auditory intervals bounded by markers ranging from 3 to 300 msec or presented as a gap within a continuous tone. As a measure of performance, difference thresholds in relation to a base duration of 50 msec were computed. Performance on temporal discrimination was significantly better with markers ranging from 3 to 150 msec than with markers ranging from 225 to 300 msec or under the gap condition. However, within each range of marker duration (3–150 msec; 225–300 msec or gap) performance did not differ significantly. A fourth experiment provided evidence that the effect of marker duration cannot be explained in terms of marker-induced masking. A good approximation of the relationship between marker duration and temporal discrimination performance in the present experiments is a smooth step function, which can account for 99.3% of the variance of mean discrimination performance. Thus, the findings of the present study point to the conclusion that two different mechanisms are used in the processing of temporal information, depending on the duration of the auditory markers. The tradeoff point for the hypothetical shift from one timing mechanism to the other may be found at a marker duration of approximately 200 msec.     

Spectral, intensive, and temporal factors influencing overshoot

Threshold was measured for a 10-msec, 4.0-kHz signal presented near the onset or in the temporal centre of a 400-msec noise masker. Overshoot, the difference (in dB) between these two thresholds, was seen only for masker bandwidths wider than a critical band. The threshold near masker onset, and hence overshoot, could be reduced by the presence of an additional noise that was presented continuously or gated on and off prior to masker onset. The spectral, intensive, and temporal properties of this effect were studied. When the additional noise was continuous and either bandpass filtered with a variable bandwidth or notch filtered with a variable notchwidth, the results indicated that energy both near and remote from the signal frequency contributed to the reduction in overshoot. The effect of this additional noise was highly dependent upon its relative level. When the additional noise was 400 msec in duration and the delay between its offset and the onset of the masker was varied, overshoot “recovered” to its maximum value within about 50 msec. Finally, as the duration of the additional noise was varied from 3 to 400 msec while the time between its offset and masker onset was fixed, the reduction in overshoot was virtually complete for durations of about 25-50 msec. The results are consistent with the notion that overshoot at least partly reflects peripheral adaptation, and that this adaptation is not restricted to the signal frequency channel but, rather, extends in both directions over several channels.     

Effects of signal duration and masker duration on detectability under diotic and dichotic listening conditions

The detectability of a 500-Hz tone of either 32- or 256-msec duration in a broad-band 50-dB spectrum level noise was measured as a function of the duration of the noise. The noise was continuous or was gated 0, 125, or 250 msec before the onset of the signal. For the gated noise conditions the noise was terminated approximately 5 msec after termination of the signal. With a homophasic condition (NO SO), the three noise conditions led to approximately the same detectability as did the continuous masker. In an antiphasic condition (NO Sπ), detectability was poorest when signal and masker began together and improved as the delay between noise onset and signal onset increased. The difference between the simultaneous onset and the continuous noise condition was about 9 dB for the 32-msec signal and about 2 dB for the 256-msec signal. These results are compared to those reported by McFadden (1966).     

A constant error in the perception of brief temporal intervals

Ss were presented two stimuli of equal duration separated in time. The parrs of stimuli were vibrotactile, auditory, or visual. The Ss adjusted the time between the two stimuli to be equal to the duration of the first stimulus. The results show that for stimulus durations ranging from 100 to 1,200 msec, Ss set the tune between the two stimuli too long and by a constant amount. For vibrotactfle stimuli, the constant was 596 msec; for auditory stimuli, 657 msec; and for visual stimuli, 436 msec. Changing the intensity of the vibrotactile stimuli did not change the size of the constant error. When Ss were presented two tones with a burst of white noise between the tones and adjusted the duration of the white noise to be equal to the duration of the first tone, the white noise was not adjusted too long by a constant amount. The results suggest that there is a constant error in the perception of unfilled relative to filled temporal intervals.     

Dichotic sequence discrimination: The effect of stimulus intensity and background noise level

Dichotic temporal discrimination of clicks over the range of separation of 2 ≤ Δt ≤ 96 msec is nonmonotonic, being V- or U-shaped with two maxima, one at very short separations (?t≤4 msec) and one at long separations (Δt ≥ 64 msec). Decreasing the level of the stimuli or increasing the level of background noise results in an overall decrement in discrimination level and a widening of the base of the function to make it more U-shaped. These effects are expressed in shorter Δt thresholds for the left limb of the function and longer Δt thresholds for the right limb of the function     

The effect of marker variability on the discrimination of temporal intervals

This research investigates the human observer’s ability to discriminate between the durations of two silent intervals, each interval preceded and followed by noise bursts called markers. The markers are separated by T or T + ΔT′ msec and T ranges from 0.3 to 1,000 msec. ΔT is defined as that value of ΔT′ for which the probability of discriminating T from T + ΔT′ is 0.75. We compared the value of AT for conditions in which the markers were fixed in amplitude and duration with conditions in which the marker amplitudes and durations were randomly chosen. ΔT increased by as much as a factor of 4 when the amplitude and duration of the markers were randomized. The performance decrement was primarily due to randomizing the first marker duration.     

Time course of chord priming

The time course of chord priming was explored in four experiments. In chord priming, a chord (a typical combination of simultaneously sounded tones) primes other chords that are musically related. In the present study, the prime duration and the stimulus onset asynchrony (SOA) between the prime chord and the chord to be judged were varied. Priming occurred at an SOA and prime duration as short as 50 msec, the shortest tested. When the prime duration was held constant at 50 msec, priming occurred at an SOA as long as 2,500 msec, the longest tested, and the magnitude of the priming effect did not diminish. To eliminate a possible role of sensory memory in maintaining the priming effect during the silence following the prime, a 250-msec noise mask was presented immediately following the 50-msec prime. The interpolated noise mask did not eliminate priming, thereby supporting the view that chord priming is the consequence of associative activation.     

Time course of chord priming.

The time course of chord priming was explored in four experiments. In chord priming, a chord (a typical combination of simultaneously sounded tones) primes other chords that are musically related. In the present study, the prime duration and the stimulus onset asynchrony (SOA) between the prime chord and the chord to be judged were varied. Priming occurred at an SOA and prime duration as short as 50 msec, the shortest tested. When the prime duration was held constant at 50 msec, priming occurred at an SOA as long as 2,500 msec, the longest tested, and the magnitude of the priming effect did not diminish. To eliminate a possible role of sensory memory in maintaining the priming effect during the silence following the prime, a 250-msec noise mask was presented immediately following the 50-msec prime. The interpolated noise mask did not eliminate priming, thereby supporting the view that chord priming is the consequence of associative activation.     

Reflex inhibition in humans: Sensitivity to brief silent periods in white noise

A white noise (60 dB SPL) was always present except for brief silent periods (“gaps”) which occurred just before an eyelid reflex was elicited in human volunteers by a brief innocuous shock to the forehead. In Experiment 1 (n=8), 10-msec gaps (“S1”) were given 40, 80, 120, 160, or 200 msec before the shock (“S2”). Compared with S2-alone trials, the reflex was inhibited by about 50% at intervals of 80 msec and beyond. Experiment 2 (n=12) first provided detection thresholds for gaps using a simple version of the method of limits: on average a gap of 5.4 msec duration was just detected. Then gaps of 0, 2, 4, 6, 8, and 10 msec were given in random order, each 100 msec before S2. The 4-msec stimulus was an effective inhibitor of the reflex, and inhibition further increased on to 6- and then to 8-msec durations. A comparison of the values obtained on reflex inhibition with the 5.4-msec threshold obtained with the conventional psycho-physical test reveals that in humans reflex inhibition provides an objective index of stimulus detection that is at least of sufficient sensitivity to warrant its clinical application. The steady increase in reflex inhibition as gap duration increased from 2 to 8 msec may be of significance for tracing the rate of decay of afferent stimulation following noise offset, as it presumably reflects the growing sensitivity to the resumption of the noise as the duration of the silent period is increased.     

Monaural and binaural temporal integration of noise bursts

Summary A comparison was made between monaural and binaural temporal integration of noise bursts at threshold. The data indicate partial integration, with approximately a 6 dB decrease in threshold per decade increase in noise burst duration for both conditions of stimulation (i.e., parallel functions) for durations ranging from 4 to 256 msec. When thresholds in dB are plotted as a function of log duration, the linear component accounts for 99% of the data indicating no essential change in the partial integration functions up to at least 256 msec. The intercept difference between the monaural and binaural integration functions is 2.5 dB.     

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.     

The effects of marker-related temporal cues on auditory gap-duration discrimination

In three experiments, we examined the ability of listeners to discriminate the duration of temporal gaps (silent intervals) and the influence of other temporal stimulus properties on their performance. In the first experiment, gap-duration discrimination thresholds were measured either in continuous noise or with noise markers with durations of 3 and 300 ms. Thresholds measured with 300-ms markers differed from those measured in continuous noise or with 3-ms markers. In the second experiment, stimuli consisting of a gap between two discrete markers were generated such that the gap duration, the onset-to-onset duration between markers, and the duration of the first marker were pseudorandomized across trials. Listeners’ responses generally were consistent with the cue that was identified as the target cue from among the three cues in each block of trials, but the data suggested that the onset-to-onset cue was particularly salient in all conditions. Using a modified method-of-adjustment procedure in the third experiment, subjects were instructed to discriminate between the durations of gaps in discrete markers of different durations in two intervals, where the gap duration in one interval was adapted to measure the point of subjective equality. Without feedback, listeners tended to equate the onset-to-onset times of the markers rather than the gap durations. Overall, the results indicated that listeners’ judgments of silent gaps between two discrete markers are strongly influenced by the onset-to-onset time, or rhythm, of the markers.     

Temporal processing capabilities in repetition conduction aphasia

This study investigates the temporal resolution capacities of the central-auditory system in a subject (NP) suffering from repetition conduction aphasia. More specifically, the patient was asked to detect brief gaps between two stretches of broadband noise (gap detection task) and to evaluate the duration of two biphasic (WN-3) continuous noise elements, starting with white noise (WN) followed by 3 kHz bandpass-filtered noise (duration discrimination task). During the gap detection task, the two portions of each stimulus were either identical (“intra-channel condition”) or differed (“inter-channel condition”) in the spectral characteristics of the leading and trailing acoustic segments. NP did not exhibit any deficits in the intra-channel condition of the gap detection task, indicating intact auditory temporal resolution across intervals of 1–3 ms. By contrast, the inter-channel condition yielded increased threshold values. Based upon the “multiple-looks” model of central-auditory processing, this profile points at a defective integration window operating across a few tens of milliseconds – a temporal range associated with critical features of the acoustic speech signal such as voice onset time and formant transitions. Additionally, NP was found impaired during a duration discrimination task addressing longer integration windows (ca. 150 ms). Concerning speech, this latter time domain approximately corresponds to the duration of stationary segmental units such as fricatives and long vowels. On the basis of our results we suggest, that the patient’s auditory timing deficits in non-speech tasks may account, at least partially, for his impairments in speech processing.     

Parameters affecting gap detection in the rat

The present research used a startle amplitude reduction paradigm to investigate the ability of the rat’s auditory system to track rapidly changing acoustic transients. Specifically examined was the ability of brief gaps in otherwise continuous noise to reduce the amplitude of a subsequently elicited acoustic startle reflex. The duration of the gap, time between gap offsetand startle elicitation (the interstimulus interval or ISI), and rise-fall characteristics of the gap were systematically varied. Consistent with previous research, gaps reliably reduced startle amplitude. Gaps 2 msec long were reliably detected, and a 50-msec ISI resulted in the greatest amplitude reduction. Gaps presented at short ISIs produced amplitude reduction that followed a different time course than did gaps presented at longer ISIs. These results may reflect differences in the length oftime available for the processing of the stimulus and may involve two different processes.     

Hemispheric asymmetries for the temporal resolution of brief auditory stimuli

This study investigates a left-hemisphere (LH) advantage for the discrimination of fine temporal events within the auditory modality in 24 normal adults. Brief noise bursts were delivered monaurally to the left or right ears, half of which contained a gap lasting between 2 and 8 msec. Subjects were required to indicate whether or not the noise burst contained a gap. Research within this area has yielded conflicting results. It is possible that variations in gap position or the properties of the noise burst may have contributed to this conflict. The effect of gap position was investigated by systematically varying the position of the gap during half of the trials. White noise bursts were used to avoid the use of spectral cues. Reaction time, response bias, and response error measures revealed a right-ear (and hence LH) advantage for gap detection. Stable gap positions were recognized more accurately than variable gap positions. Gap position had no effect on the observed LH advantage. These results suggest that the auditory properties of noise burst, rather than gap position, play an important role in the discrepancies observed in this area.     

Time-shrinking: A discontinuity in the perception of auditory temporal patterns

Recent research at our laboratories in the field of human auditory time perception revealed that the duration of short empty time intervals (<～200 msec) is considerably underestimated if they are immediately preceded by shorter time intervals. Within a certain range, the amount of subjective time shrinking is a monotonous function of the preceding time interval: the shorter it is, the more it shrinks its successor. In the present study, the preceding interval was kept constant at 50 msec, and the following interval for which the duration had to be judged, varied from 40 to 280 msec. The results showed that at up to 100 msec, the perceived duration increased to a much lesser extent than did the objective duration. Beyond 120 msec, the perceived duration quickly increased and reached a veridical value at 160 msec. Such a sudden change of perceived duration in a temporal pattern in which the objective duration varies gradually indicates a typical example of categorical perception. We suggest that such a categorization of the time dimension might be a clue for processes of speech and music perception.     

Hemispheric asymmetries for temporal information processing: transient detection versus sustained monitoring

This study investigated functional differences in the processing of visual temporal information between the left and right hemispheres (LH and RH). Participants indicated whether or not a checkerboard pattern contained a temporal gap lasting between 10 and 40 ms. When the stimulus contained a temporal signal (i.e. a gap), responses were more accurate for the right visual field-left hemisphere (RVF-LH) than for the left visual field-right hemisphere (LVF-RH). This RVF-LH advantage was larger for the shorter gap durations (Experiments 1 and 2), suggesting that the LH has finer temporal resolution than the RH, and is efficient for transient detection. In contrast, for noise trials (i.e. trial without temporal signals), there was a LVF-RH advantage. This LVF-RH advantage was observed when the entire stimulus duration was long (240 ms, Experiment 1), but was eliminated when the duration was short (120 ms, Experiment 2). In Experiment 3, where the gap was placed toward the end of the stimulus presentation, a LVF-RH advantage was found for noise trials whereas the RVF-LH advantage was eliminated for signal trials. It is likely that participants needed to monitor the stimulus for a longer period of time when the gap was absent (i.e. noise trials) or was placed toward the end of the presentation. The RH may therefore be more efficient in the sustained monitoring of visual temporal information whereas the LH is more efficient for transient detection.     

Word recognition with masking

At illuminances between .07 and 17 ft.-c, the word-recognition threshold was lower when a common word was preceded and followed by a homogenous field than by a noise pattern composed of a random array of bits of letters. Most of the difference is ascribed to the pattern’s interference with post-stimulatory processes. This interference may explain why with masking the threshold reached a minimum at 90 msec. and then did not decrease further despite increasing illuminance, whereas without masking the threshold continued to decrease down to 7 msec, the shortest duration tested.     

Shrinkage in the perceived duration of speech and tone by acoustic replacement1

Abstract: To investigate mechanisms for perceiving the duration of an auditory event, an effect of perceptual grouping upon perceived duration was studied psychophysically. In the first experiment, the perceived duration of a spoken word was measured under three conditions of acoustic continuity (i.e., (a) intact, (b) noise‐replaced, and (c) gap‐replaced) as a function of the duration of the target stimulus. Under the noise‐replaced condition, a portion of the target stimulus was physically replaced with a noise burst. Under the gap‐replaced condition, the replacement was made with a gap. The gap‐replacement resulted in a prominent shrinkage of the perceived duration. In the case of noise‐replacement, the amount of shrinkage was moderate but highly significant, although the word employed was perceived to be phonetically intact. Independent of this effect of replacement, the amount of shrinkage was also affected by the physical duration of the target stimulus. The second experiment tested an effect of noise replacement on the perceived duration of a tone burst. In this case, the noise replacement also shrunk the perceived duration of the non‐speech stimulus. This noise‐induced shrinkage could be regarded as being general for the auditory duration. The phenomenon is discussed in relation to a revised model for perceived duration.