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).     

Effect of masker level on infants’ detection of tones in noise

In adult listeners, the signal-to-noise ratio at masked threshold remains constant with increases in masker level over a wide range of stimulus conditions. This relationship was examined in 7-month-old infants by obtaining masked thresholds for .5- and 4-kHz tones presented in four levels of continuous masking noise. Adults were also tested for comparison. Masker spectrum levels ranged from 5 to 35 dB/Hz for .5-kHz tones, and from ?5 to 25 dB/Hz for 4-kHz stimuli. Thresholds were determined for stimuli of both 10 and 100 msec in duration. The results indicated that infants’ performance was more adultlike for 4-kHz stimuli. Although mean thresholds for both 10- and 100-msec, 4-kHz tones were approximately 7 dB higher in infants than in adults, E/N₀ at threshold remained essentially constant over the 30-dB range of maskers employed. By contrast, infants’ thresholds for .5-kHz tones were exceptionally high at lower levels of the masker. Threshold E/N0 decreased significantly as masker level increased from 5 to 35 dB/Hz, and this decrease was significantly greater for 10- than for 100-msec stimuli. Temporal summation of .5-kHz tones, measured as the difference between thresholds obtained at the two signal durations, was greater for infants than for adults at low levels of the masker. However, because infants’ thresholds improved more rapidly with level for 10- than for 100-msec tones, age differences in temporal summation were no longer significant when masker spectrum level was 35 dB/Hz. These results suggest that the relationship between signal-to-noise ratio at masked threshold and level of the masker is dependent on both signal frequency and duration during infancy.     

Some nonmasking auditory postsignal effects

Observers were asked to detect a 20-msec segment of a sinusoidal signal masked by a band-limited white noise. A postsignal decrease in the spectrum level of the noise within the critical band of the signal enhanced the detectability of that signal if the decrease occurred within approximately 25 msec following signal termination. Postsignal decreases outside the critical band of the signal, and decreases within the critical band delayed longer than approximately 40 msec, reduced the detectability of the signal for decrease delays up to between approximately 150 and 400 msec, depending on the spectral characteristics of the decrease. Comparisons with typical backward masking results indicate probable common factors of short-term temporal summation and longer term attention.     

Effect of masker level on infants' detection of tones in noise

In adult listeners, the signal-to-noise ratio at masked threshold remains constant with increases in masker level over a wide range of stimulus conditions. This relationship was examined in 7-month-old infants by obtaining masked thresholds for .5- and 4-kHz tones presented in four levels of continuous masking noise. Adults were also tested for comparison. Masker spectrum levels ranged from 5 to 35 dB/Hz for .5-kHz tones, and from -5 to 25 dB/Hz for 4-kHz stimuli. Thresholds were determined for stimuli of both 10 and 100 msec in duration. The results indicated that infants' performance was more adult-like for 4-kHz stimuli. Although mean thresholds for both 10- and 100-msec, 4-kHz tones were approximately 7 dB higher in infants than in adults, E/N0 at threshold remained essentially constant over the 30-dB range of maskers employed. By contrast, infants' thresholds for .5-kHz tones were exceptionally high at lower levels of the masker. Threshold E/N0 decreased significantly as masker level increased from 5 to 35 dB/Hz, and this decrease was significantly greater for 10- than for 100-msec stimuli. Temporal summation of .5-kHz tones, measured as the difference between thresholds obtained at the two signal durations, was greater for infants than for adults at low levels of the masker. However, because infants' thresholds improved more rapidly with level for 10- than for 100-msec tones, age differences in temporal summation were no longer significant when masker spectrum level was 35 dB/Hz. These results suggest that the relationship between signal-to-noise ratio at masked threshold and level of the masker is dependent on both signal frequency and duration during infancy.     

Saccade latency and warning signals: Stimulus onset,offset, and change as warning events

Two experiments investigated saccade latency to a peripheral target under various warning signal conditions. In Experiment I, the effects of warning stimulus onset, change, and two offset conditions were compared at warning intervals of 0, 100, 300, and 600 msec. Warning stimulus onset, change, and offset were all effective in reducing saccade latency as compared to a no-warning control condition, but warning stimulus offset resulted in shorter saccade latency than onset or change at all warning intervals. Experiment 2 compared onset and offset warning conditions at ?300-, ?250-, ?200-, ?150-, ?100-, ?50-, 0-, and 50-msec intervals. Responses following onset were slower than those following offset at the latter five intervals, while warning onset resulted in slower saccades than no-warning control conditions at ?150-, ?100-, and ?50-msec intervals. These results indicate that the onset of a visual warning signal can have an interfering effect on the programming or execution of a saccade.     

Persistence and integration: Two consequences of a sliding integrator

The detection of a silent interval, or gap, placed in the temporal center of a gated noise burst was investigated. The gated noise masker ranged from 2 to 400 msec in duration. For long noises, the duration, Δ, of the just-detectable gap remained fixed at about 2.8 msec. Progressively shortening the duration of the noise did not affect Δ until the duration was approximately 20 msec; thereafter, decreasing the noise duration improved detectability of the gap. In a second experiment, continuous noise filled the temporal gap, although the decibel difference between the noise in the gap and the noise surrounding the gap was always at least 5 dB. The level of noise filling the gap did not greatly affect Δ. The third experiment was similar to the first, except that the signal was a click rather than a gap. The results for both gaps and clicks were fitted by a model assuming a sliding integrator.     

Frequency selectivity using tonal-temporal masking: Diotic vs. dichotic masking

A combined forward-backward masking procedure was used to investigate the threshold of a 30-msec, 500-Hz signal as a function of masker frequency. The signal thresholds were obtained in two signal conditions, diotic (So) and dichotic (S_π), and for two different temporal separations of the maskers. The maskers were 500 msec in duration and were presented at 75 dB SPL. The function relating masked signal threshold to masker frequency was used to describe frequency selectivity in the four conditions. There were no differences in frequency selectivity measured between the diotic and dichotic signal conditions and only a small difference measured between the two intermasker interval conditions. The S_π conditions yielded lower thresholds than did the So conditions. The change in intermasker interval from 10 to 50 msec lowered the threshold maximally 18 dB for the So condition and 13 dB for the S_π condition. The results indicate that in this tonal temporal masking procedure there are no differences between the diotic and dichotic critical bands.     

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.     

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.     

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.     

Perception without awareness: further evidence from a Stroop priming task

In the present research, we examined the influence of prime-target stimulus onset asynchrony (SOA) on Stroop-priming effects from masked words. Participants indicated the color of a central target, which was preceded by a 33-msec prime word followed either immediately or after a variable delay by a pattern mask. The prime word was incongruent or congruent with the target color on 75% and 25% of the trials, respectively. The words followed by an immediate mask produced reliable Stroop interference at SOAs of 300 and 400 msec but not at SOAs of 500 and 700 msec. The words followed by a delayed mask produced a reversed (i.e., facilitatory) Stroop effect, which reached significance at an SOA of 400 msec or longer, but never at the shorter 300-msec SOA. Such an differential time course of both types of Stroop priming effects provides further evidence for the existence of qualitative differences between conscious and nonconscious perceptual processes.     

Masking of tones by tones and of noise by noise

Using a two-alternative temporal forced-choice technique, two binaural detection experiments were performed. In the first, the detectability of a 250-Hz 128-msec tonal signal masked by a gated 70-dB SPL tone of the same frequency and duration was measured as a function of the level of the signal, the phase angle at which the signal was added to the masker, and the interaural phase difference of the signal. In the second experiment, the signal was a wideband (100-3,000 Hz) 128-msec Gaussian noise masked by a continuous Gaussian noise of the same bandwidth and coherent with the signal. The detectability of this noise signal was measured as a function of the same variables investigated in the first experiment. In both experiments detectability was found to follow a simple energy- or power-detection model when the interaural phase difference was 0 deg. When the interaural phase difference was 180 deg, the function relating the signal level required for a constant level of performance to the signal-masker phase angle is such that neither the Webster-Jeffress hypothesis nor Durlach’s E-C model accounts for the data. The data are reasonably well fit by a model proposed by Hafter and Carrier.     

An anxiety-related bias in semantic activation when processing threat/neutral homographs

Three experiments are reported comparing high and low-trait anxious subjects in terms of their patterns of semantic activation in response to ambiguous primes, with one threat-related and one neutral meaning. Such primes were followed by targets related to either their threat or neutral meaning, or by unrelated targets, in a lexical decision task. Experiments 1 to 3 employed stimulus onset asynchronies (SOAs) of 750 msec, 500 msec, and 1250 msec, respectively. At 500-msec SOA all subjects showed facilitation for both meanings. At 750-msec SOA the only significant priming effect was that for the threat-related meaning in the high-anxiety group, and a similar trend was found at 1250-msec SOA. Consideration of the patterns of priming for targets following ambiguous threat/neutral primes suggest that at the longer SOAs, high-anxiety subjects consciously “lock on” to a threatening interpretation if one has been made available by earlier automatic spreading activation.     

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.     

Is desynchrony tolerance adaptable in the perceptual organization of speech?

Speech signal components that are desynchronized from the veridical temporal pattern lose intelligibility. In contrast, audiovisual presentations with large desynchrony in visible and audible speech streams are perceived without loss of integration. Under such conditions, the limit of desynchrony that permits audiovisual integration is also adaptable. A new project directly investigated the potential for adaptation to consistent desynchrony with unimodal auditory sine-wave speech. Listeners transcribed sentences that are highly intelligible, with veridical temporal properties. Desynchronized variants were created by leading or lagging the tone analog of the second formant relative to the rest of the tones composing the sentences, in 50-msec steps, ranging from 250-msec lead to 250-msec lag. In blocked trials, listeners only tolerated desynchronies <50 msec, and exhibited no gain in intelligibility to consistent desynchrony. Unimodal auditory and bimodal audiovisual forms of perceptual integration evidently exhibit different temporal characteristics, an indication of distinct perceptual functions.     

The time course of attention in a simple auditory detection task

What is the time course of human attention in a simple auditory detection task? To investigate this question, we determined the detectability of a 20-msec, 1000-Hz tone presented at expected and unexpected times. Twelve listeners who expected the tone to occur at a specific time after a 300-msec narrowband noise rarely detected signals presented 150-375 msec before or 100-200 msec after that expected time. The shape of this temporal-attention window depended on the expected presentation time of the tone and the temporal markers available in the trials. Further, though expecting the signal to occur in silence, listeners often detected signals presented at unexpected times during the noise. Combined with previous data, these results further clarify the listening strategy humans use when trying to detect an expected sound: Humans seem to listen specifically for that sound, while ignoring the background in which it is presented, around the time when the sound is expected to occur.     

Binaural interaction in backward masking

The binaural auditory system exhibits certain advantages over the monaural system when detecting a tonal signal in a background of masking noise. These advantages have been described in detail and are referred to as masking-level differences, or MLDs. It has been demonstrated, for example, that performance in detecting a tonal signal that has been reversed in phase at one ear relative to the other ear is about 15–17 dB better than detection of the same signal in-phase at the two ears when masked by moderately intense masking noise that is in-phase at the two ears. The explanations for this phenomenon fall into two general categories, and both types of explanations are based upon the interaction of the tonal signal and masker when they are added together. In the present paper, data are presented which indicate that an MLD of at least 4–5 dB can be obtained in a binaural masking experiment in which the offset of the tonal signal precedes the onset of the noise masker.     

Effect of “backward” masker fringe on the detectability of pulsed diotic and dichotic tonal signals

The effects of backward masker “fringe” on performance in homophasic and antiphasic masking conditions were investigated. The results of the study indicate that (1) the presence of a backward masker fringe has only a small effect on performance in homophasic masking conditions; (2) under antiphasic masking conditions, the presence of a backward masker fringe improves performance; (3) similar to the results of studies investigating the effects of forward masker fringe, the magnitude of the improvement in performance increases as the duration of the fringe increases; and (4) the magnitude of the improvement caused by the presence of backward masker fringe is considerably smaller than the magnitude of the improvement caused by the forward masker fringe. It appears, then, that the presence of backward masker fringe may provide a baseline or reference phase similar to that which the forward fringe is presumed to provide. The presence of this reference phase after the offset of the signal apparently makes the phase shift associated with the signal-plus-noise waveform more discernible, thus leading to higher detectability. However, for reasons not yet clear, the presence of a baseline or reference phase after the offset of the signal (backward fringe conditions) does not make the signal-plus-noise phase shift as discernible as do either the presence of that same reference phase before the onset of the signal (forward fringe condition) or the presence of that same reference phase both before signal onset and after signal offset (continuous masker condition).     

Relative contributions of envelope maxima and minima to comodulation masking release

Comodulation masking release (CMR) is a phenomenon that demonstrates the sensitivity of the auditory system to across-frequency differences in the temporal modulation pattern of a complex waveform. In this paper, we review briefly some of the data on the physical parameters that affect CMR and describe models that have been proposed to account for CMR -- namely, models based upon envelope equalization/cancellation, across-frequency envelope correlation, and “dip listening”. The present literature is ambiguous with regard to the relative importance of energy in the peak and dip regions of the waveform envelope. We therefore performed a series of experiments to investigate this issue. In the first experiment, we examined CMR for signals that resulted either in a uniform increment or in uniform decrement in the masking noise centred on the signal frequency. This was accomplished by using a 20-Hz-wide noise band centred on 700 Hz as both the masker and as the signal, adjusting the phase angle between the signal and masker to either 0° (increment) or 180° (decrement). Conditions were examined where either zero, one, two, four, or six comodulated flanking bands were present. Results indicated positive CMRs for all conditions in which a comodulated flanking band was present. CMR increased as the number of flanking bands increased for intensity increments, but not for intensity decrements. The remaining experiments examined conditions where signals were present only in masker peaks, or only in masker dips. The results of these experiments indicated relatively large CMRs when the signal occurred in dip regions, but no CMR when the signal occurred in peak regions. Whereas some of the results of the above experiments would be difficult to account for in terms of the dip listening hypothesis of CMR, the present findings did indicate that the stimulus cues that give rise to CMR appear to be derived primarily from the dip regions of the masking noise.