Pitch memory for short tones

Ten listeners judged a 300-msec tone as higher or lower in pitch than another 300-msec tone that occurred 8 sec earlier. The intervening time either was unfilled or contained a 400-msec interpolated tone. This interpolated tone occurred either just after the first tone or just before the final one, and was of a frequency either inside or outside the critical band of the target frequency. Performance for the silent-interval condition was about as good as has been reported for pitch discrimination with no delay when the target was 250 Hz but was slightly poorer for the target at 1,550 Hz. Presence of the interpolated tone decreased the slope of the psychometric [unction and produced constant error for nine Ss. These effects were more pronounced when the interpolated tone occurred 50 msec after the target than when it preceded the comparison tone by 50 msec. Both brevity of the target tone and occurrence soon thereafter of an interpolated tone are required to produce constant errors of pitch memory.     

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).     

Diotic and dichotic frequency recognition in a single-interval temporal interference procedure

The frequency discriminability of a 70-dB SPL, 20-msec test tone followed 5 msec later by an equally intense 500-msec, 800-Hz interference tone was studied in a single-interval procedure for one diotic condition and three dichotic conditions. The test tone (T) and interference tone (I) were presented the same to both ears (ToIo, diotic condition) and in three dichotic conditions: (1) the interference tone was presented to the right ear (R) and the test tone to the left ear (L) (T_LI_R), (2) the interference tone was presented the same to both ears and the test tone to one ear (TmIo), and (3) the interference tone was presented the same to both ears and the test tone to both ears with an interaural phase reversal (TπIo). The threshold value for test tone frequency discrimination in the diotic temporal interference condition was approximately six times greater than that obtained without an interference tone. The three dichotic temporal interference conditions yielded essentially equivalent threshold values which were approximately 2.4 times that obtained when the test tone was presented without an interference tone. Therefore, although never equaling interference-free conditions, dichotic test tone presentations can improve frequency recognition relative to diotic conditions at intensities well above threshold. It is postulated that this improvement may be due to the spatial separation of test and interfering tones, rather than to possible differences in diotic vs. dichotic subjective intensities. Dichotic-diotic frequency recognition differences did not occur when a 100-msec interval separated the test and interfering tone or when the interfering tone preceded the test tone.     

Infants’ detection of increments in low- and high-frequency noise

A visually reinforced operant paradigm was employed to examine the relationship between the difference limen (DL) for intensity and level of the standard during infancy. In Experiment 1,7-month-old infants and adults detected increments in continuous noise presented via headphones at each of four levels ranging from 28 to 58 dB SPL. Noise stimuli were 2-octave bands centered at either 400 or 4000 Hz, and increments were 10 and 100 msec in duration. Infants’ DLs were significantly larger than those of adult subjects and significantly larger for low- than for high-frequency stimuli. For the high-frequency noise band, infants’ DLs were generally consistent with Weber’s law,remaining essentially constant for standards higher than 28 dB SPL (3 dB SL) for 100-msec increments and 38 dB SPL (13 dB SL) for 10-msec increments. For low-frequency noise, infants’ absolute thresholds were exceptionally high, and sensation levels of the standards were too low to adequately describe the relationship. In Ex-periment 2, 7-month-old infants detected 10- and 100-msec increments in 400-Hz noise stimuli presented in sound field. Infants’ low-frequency DLs were large at low intensities and decreased with increases in level of the standard up to at least 30 dB SL. For both low- and high-frequency noise, the difference between DLs for 10- and 100-msec increments tended to be large at low levels of the standard and to decrease at higher levels. These results suggest that the relationship between the DL and level of the standard varies with both stimulus frequency and duration during infancy. However, stimulus-dependent immaturities in increment detection may be most evident at levels within approximately 30 dB of absolute threshold.     

Asynchrony tolerance in the perceptual organization of speech

Researchers have claimed that listeners tolerate large temporal distortion when integrating the spectral components of speech. In some estimates, perceivers resolve linguistic attributes at spectral desynchronies as great as the duration of a syllable. We obtained new measures of perceptual tolerance of auditory asynchrony, using sine-wave synthesis in order to require perceivers to resolve the speech stream dynamically. Listeners transcribed sentences in which the tone analogue of a second formant was desynchronized relative to the remaining tones of a sentence, with desynchrony ranging from a 250-msec lead to a 250-msec lag. Intelligibility declined symmetrically from 72% at synchrony to 7% at 6100 msec. This finding of narrow asynchrony tolerance indicates a time-critical feature of the auditory perceptual organization of speech     

Facultative and inhibitory effects of location and frequency cues: Evidence of a modulation in perceptual sensitivity

The possibility that facilitative and inhibitory effects of auditory cues result because of a modulation in perceptual sensitivity was examined. Listeners were presented with a cue followed by a target, with the time period between the two varied at stimulus onset asynchronies (SOAs) of 150,450, or 750 msec. In two conditions, the cue and target were either the same or different in location or frequency. In both conditions, listeners were required to identify the rise time of the target. Whereas the cue was presented in isolation, the target was presented in a wide-band noise background such that the required discrimination was made relatively difficult. In both conditions, a facilitative effect was apparent at the 150-msec SOA and an inhibitory effect was apparent at the 750-msec SOA for both accuracy and response time measures of performance. That these results were apparent for a judgment unrelated to the manipulated cue-target relation suggests strongly that both location-based and frequency-based auditory inhibition of return result primarily because of changes in perceptual sensitivity.     

Facilitative and inhibitory effects of location and frequency cues: evidence of a modulation in perceptual sensitivity.

The possibility that facilitative and inhibitory effects of auditory cues result because of a modulation in perceptual sensitivity was examined. Listeners were presented with a cue followed by a target, with the time period between the two varied at stimulus onset asynchronies (SOAs) of 150, 450, or 750 msec. In two conditions, the cue and target were either the same or different in location or frequency. In both conditions, listeners were required to identify the rise time of the target. Whereas the cue was presented in isolation, the target was presented in a wide-band noise background such that the required discrimination was made relatively difficult. In both conditions, a facilitative effect was apparent at the 150-msec SOA and an inhibitory effect was apparent at the 750-msec SOA for both accuracy and response time measures of performance. That these results were apparent for a judgment unrelated to the manipulated cue-target relation suggests strongly that both location-based and frequency-based auditory inhibition of return result primarily because of changes in perceptual sensitivity.     

Transfer of learning across durations and ears in auditory frequency discrimination

Frequency-discrimination thresholds (FDTs) for 1-kHz tone pips with durations of 40, 100, and 200 msec were measured in the left and right ears of 10 normal-hearing listeners, before and after six 2-h frequency-discrimination training sessions involving, exclusively, the 200-msec duration and the right ear. In the trained ear, highly significant improvements in FDTs were observed at all durations. Further inspection of the data suggested complete generalization between 200 and 100 msec, but not at 40 msec. Posttraining FDTs were not found to differ between the two ears for the two untrained durations, but proved significantly smaller in the right (trained) than in the left (untrained) ear at the trained (200-msec) duration only. A control experiment involving 10 additional subjects allowed us to establish the absence of intrinsic differences in pretraining FDTs between the right and left ears. Overall, these findings indicate that frequency-discrimination learning generalizes widely across stimulus durations and across ears, but that part of the improvement is specific to the range of durations and to the ear used in training.     

Frequency recognition in temporal interference tasks: A comparison among four psychophysical procedures

The frequency discrimination of a 20-msec test tone was measured for the same subjects in four psychophysical paradigms: a single-interval procedure, a two-alternative forced-choice procedure, a same-different procedure, and a method-of-adjustment procedure. In each paradigm, the 20-msec test tone was preceded or followed by a 500-msec, 800-Hz interfering tone. The interfering tone occurred 50 or 5 msec before the onset of the test tone (forward interference) or 100 or 5 msec after the offset of the test tone (backward interference). In each of the four paradigms and for each of the interference conditions the value of Δf for the test tone was varied symetrically around 800 Hz to obtain an estimate of the frequency discrimination thresholds. In all psychophysical paradigms except for the single-interval procedure, there were small or no significant differences in observers’ frequency discrimination behavior among the interference conditions. The thresholds for Δf from these conditions were approximately the same as those obtained without an interfering tone. In the single-interval task, when the test tone preceded the interfering tone (backward interference) by 5 msec, an increase in the value of Δf required for discrimination over that required in the other conditions was measured. These results suggest that the effect of backward interference on a target tone does depend on psychophysical procedure.     

Preferred perceptual tempo for sound sequences: comparison of adults, children, and infants

Previous motor and perceptual tasks have found optimal processing for sound sequences of a rate of around 600 msec. IOI (Interonset Interval). This zone of optimal processing (the rate at which discrimination is optimal) slows with age and is also found with infants. The current work investigated whether listeners "prefer" sequences at the rate for which they demonstrate optimal processing. In the present study, three experiments were done. Exp. 1 measured tempo preferences in adults who listened to pairs of isochronous sound sequences varying in tempo (from 100- to 1500-msec. IOI) and were required to indicate which they preferred. As expected, highest preferences were expressed for the intermediate tempi, supporting the hypothesis of a zone of preferred tempi comparable to the zone of optimal processing. Moreover, this preference for intermediate tempi was not affected by the temporal context (absence of differences between a fast, a slow, and a wide set of tempi). In Exp. 2, the same procedure was applied to 6- and 10-yr.-olds. Children in both groups had systematic preferences for the fastest tempi within a set, and the older children generally preferred slower sequences. Exp. 3 used a preference paradigm for sound sequences with 4-mo.-old infants, comparing sequences of 100- vs 300-msec. IOI, 300- vs 900-msec. IOI, and 100- vs 900-msec. IOI. No systematic tempo preferences were observed. We conclude that tempo discrimination and tempo preference may have some commonality (perhaps related to a zone of optimal processing), especially in adults, but that they also involve quite distinct processes which undergo different developmental sequences. Whereas adults prefer what they process the best, children prefer what is fastest (and therefore more attention-getting), and we have not been able to detect preferences in infants.     

Frequency-shift detectors bind binaural as well as monaural frequency representations

Previous psychophysical work provided evidence for the existence of automatic frequency-shift detectors (FSDs) that establish perceptual links between successive sounds. In this study, we investigated the characteristics of the FSDs with respect to the binaural system. Listeners were presented with sound sequences consisting of a chord of pure tones followed by a single test tone. Two tasks were performed. In the "present/absent" task, the test tone was either identical to one of the chord components or positioned halfway in frequency between two components, and listeners had to discriminate between these two possibilities. In the "up/down" task, the test tone was slightly different in frequency from one of the chord components and listeners had to identify the direction (up or down) of the corresponding shift. When the test tone was a pure tone presented monaurally, either to the same ear as the chord or to the opposite ear, listeners performed the up/down task better than the present/absent task. This paradoxical advantage for directional frequency shifts, providing evidence for FSDs, persisted when the test tone was replaced by a dichotic stimulus consisting of noise but evoking a pitch sensation as a consequence of binaural processing. Performance in the up/down task was similar for the dichotic stimulus and for a monaural narrow-band noise matched in pitch salience to it. Our results indicate that the FSDs are insensitive to sound localization mechanisms and operate on central frequency representations, at or above the level of convergence of the monaural auditory pathways.     

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.     

Facilitative and inhibitory effects of cuing sound duration, intensity, and timbre.

Two experiments are reported in which the possibility that auditory attention may be controlled in a stimulus-driven manner by duration, intensity, and timbre cues was examined. In both experiments, listeners were presented with a cue followed, after a variable time period of a 150-, 450-, or 750-msec stimulus onset asynchrony (SOA), by a target. In three different conditions for each experiment, the duration, intensity, or timbre relation between the cue and the target was varied so that, on 50% of the trials, the two sounds were identical and, on 50% of the trials, the two sounds were different in the manipulated feature. The two experiments differed only in the judgment required, with listeners in Experiment 1 identifying the duration, intensity, or timbre of the target and listeners in Experiment 2 indicating whether the target incorporated a brief silent gap. In both experiments, performance was observed to depend on both the similarity of and the time between the cue and the target. Specifically, whereas at the 150-msec SOA performance was best when the target was identical to the preceding cue, at the 750-msec SOA performance was best when the cue and the target differed. This pattern establishes the existence of duration-, intensity-, and timbre-based auditory inhibition of return. The theoretical implications of these results are considered.     

Facilitative and inhibitory effects of cuing sound duration, intensity, and timbre

Two experiments are reported in which the possibility that auditory attention may be controlled in a stimulus-driven manner by duration, intensity, and timbre cues was examined. In both experiments, listeners were presented with a cue followed, after a variable time period of a 150-, 450-, or 750-msec stimulus onset asynchrony (SOA), by a target. In three different conditions for each experiment, the duration, intensity, or timbre relation between the cue and the target was varied so that, on 50% of the trials, the two sounds were identical and, on 50% of the trials, the two sounds were different in the manipulated feature. The two experiments differed only in the judgment required, with listeners in Experiment 1 identifying the duration, intensity, or timbre of the target and listeners in Experiment 2 indicating whether the target incorporated a brief silent gap. In both experiments, performance was observed to depend on both the similarity of and the time between the cue and the target. Specifically, whereas at the 150-msec SOA performance was best when the target was identical to the preceding cue, at the 750-msec SOA performance was best when the cue and the target differed. This pattern establishes the existence of duration-, intensity-, and timbre-based auditory inhibition of return. The theoretical implications of these results are considered.     

Auditory-visual conflicts in the perceived duration of lights, tones and gaps

The perceived duration of a short tone (1,000 or 1,500 msec) was longer than that of a separately presented light of equal length. Thus, when light and tone were presented simultaneously, there was a conflict in perceived duration. In that case, the perceived duration of an interval filled with both light and tone was close to that of an interval filled with tone alone. A silent gap in otherwise continuous tone was perceived as longer than a gap in otherwise continuous light, and the perceived duration of a gap occurring simultaneously in both light and tone was close to that of a gap in tone alone. Thus, auditory dominance occurred under the preceding conditions-that is, auditory-visual conflicts in perceived duration, whether occurring between filled intervals or gaps, were resolved in favor of the auditory modality. Visual dominance occurred only under one condition, in which the intensity of tone was reduced, and in which the perceived duration of a 500-msec light was longer than that of a 500-msec tone. The finding of auditory dominance in the perception of time runs counter to the results of studies of sensory conflicts in spatial perception, where vision typically dominates audition and touch.     

Tweaking the lexicon: organization of vowel sequences into words

The ability of listeners to distinguish between different arrangements of the same three vowels was investigated for repeating sequences having item durations ranging from 10 msec (single glottal pulses) up to several seconds/vowel. Discrimination was accomplished with ease by untrained subjects at all item durations. From 30 through 100 msec/vowel, an especially interesting phenomenon was encountered: The sequences of steady-state vowels were organized into words, with different words heard for the different arrangements of items. In a second experiment, repeating sequences of random arrangements of 10 40-msec vowels were employed. When sets of four such sequences were presented to listeners, distinctive words were heard, which permitted each arrangement to be discriminated from the others. In addition, minimal differences (reversing the order of a single contiguous pair of vowels) in the 10-item sequences could be detected via verbal mediation. Hypotheses are offered concerning mechanisms responsible for these results.     

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.     

Response differentiation to facial expression of emotion as increasing exposure duration

This study investigated whether the underlying structure of responses to facial expressions of emotion would emerge when the exposure time was increased. 25 participants judged facial photographs presented for varying durations of exposure, ranging from 4 msec. to 64 msec. in 4-msec. steps. A dual scaling method was carried out to analyze possible response differentiation as a function of exposure time. Two major components were extracted. Based on the configuration of variables they were interpreted as valence (hedonic tone) and activation. Results indicated that a positive emotion and a highly activated emotion such as surprise and fear were easily recognized under a relatively brief exposure to the stimuli.     

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.