A release from masking by continuous, random, notched noise

Thresholds for 10-ms sinusoids simultaneously masked by bursts of bandpass noise centered on the signal frequency were measured for a wide range of signal frequencies and noise levels. Thresholds were defined as the signal power relative to the masker power at the output of an auditory filter centered on the signal frequency. It was found that the presentation of a continuous random noise, with a spectral notch centered on the signal frequency, produced a reduction in signal thresholds of up to 11 dB. A notched noise spectrum level of 0-5 dB above that of the masker proved most effective in producing a masking release, as measured by a reduction in masked threshold. A release from masking of up to 7 dB could be obtained with a continuous bandpass noise. The most effective spectrum level of this noise was 5 dB below that of the masker. The effect of the continuous notched noise was to reduce signal-to-masker ratios at threshold to about 0 dB, regardless of the threshold in the absence of continuous noise. Thus the greatest release from masking occurred when "unreleased" thresholds were highest. The release from masking is almost complete within 320 ms of notched noise onset, and persists for about 160 ms after notched noise offset, regardless of notched noise level. The phenomenon is similar in many ways to the "overshoot" effect reported by Zwicker [J. Acoust. Soc. Am. 37, 653-663 (1965)]. It is argued that both effects can be largely attributed to peripheral short-term adaptation, a mechanism which is also believed to be involved in forward masking.     

Spectral and level effects in noise-on-tone suppression

The effective internal level of a 1-kHz tone at 50 dB SPL was estimated by measuring the forward masking produced on a 10-ms signal tone of the same frequency. Noise containing a spectral notch was then added to the masker tone, and its influence on the effective level of the tone was measured with a variety of noise levels, notch widths, and notch shapes. In experiment 1, the masker tone was centered in the spectral notch, itself centered in a 2-kHz band of noise. As the spectrum level in the noise passbands increased from 6 dB/Hz to 36 dB/Hz, signal threshold decreased, indicating a decrease in masking by the masker tone. This "unmasking" effect of the noise was attributed to suppression of the masker tone by the components in the noise. Unmasking was greatest with the narrowest spectral notch (250 Hz), and decreased to zero as the notch widened to 1500 Hz. Compared to its level when presented alone, the effective internal level of the masker tone could be reduced by up to 30 dB (250-Hz notch, 36 dB/Hz). The relative suppressive strength of individual noise components was estimated in experiment 2, in which the 1-kHz masker tone was located at one edge of a spectral notch, rather than in the center. Noise spectrum level was fixed at 16 dB/Hz. As notch width decreased to zero, on either the high-frequency or low-frequency side of the masker tone, its effective internal level was again reduced by approximately 30 dB. In a tentative analysis, the first derivative of the smoothed threshold function was taken, to provide an estimate of the relative contributions to suppression at 1 kHz of noise components between 250 and 1740 Hz.(ABSTRACT TRUNCATED AT 250 WORDS)     

Comparisons of frequency selectivity in simultaneous and forward masking for subjects with unilateral cochlear impairments

Two experiments are described in which frequency selectivity was estimated, in simultaneous and forward masking, for each ear of subjects with moderate (25-60 dB HL) unilateral cochlear hearing losses. In both experiments, the signal level was fixed for a given ear and type of masking (simultaneous or forward), and the masker level was varied to determine threshold, using an adaptive, two-alternative forced-choice procedure. In experiment I, the masker was a noise with a spectral notch centered at the signal frequency (either 1.0 or 1.5 kHz); threshold was determined as a function of notch width. Signal levels were chosen so that the noise level required at threshold for a notch width of zero was similar for the normal and impaired ear of each subject in both simultaneous and forward masking. The function relating threshold to notch width had a steeper slope for the normal ear than for the impaired ear of each subject. For the normal ears, these functions were steeper in forward masking than in simultaneous masking. This difference was interpreted as resulting from suppression. For the impaired ears, significant differences in the same direction were observed for three of the five subjects, but the differences were smaller. In experiment II, psychophysical tuning curves (PTCs) were determined in the presence of a fixed notched noise centered at the signal frequency (1.0 kHz). For the normal ears, the PTCs were sharper in forward masking than in simultaneous masking. For the impaired ears, the PTCs were similar in simultaneous and forward masking, but those in forward masking tended to be sharper at masker frequencies far removed from the signal frequency. Overall, the results suggest that suppression is reduced, but not completely absent in cases of moderate cochlear hearing loss.     

The temporal course of masking and the auditory filter shape

Recent experiments have shown that frequency selectivity measured in tone-on-tone simultaneous masking improves with increasing delay of a brief signal relative to the onset of a longer duration gated masker. To determine whether a similar improvement occurs for a notched-noise masker, threshold was measured for a 20-ms signal presented at the beginning, the temporal center, or the end of the 400-ms masker (simultaneous masking), or immediately following the masker (forward masking). The notch width was varied systematically and the notch was placed both symmetrically and asymmetrically about the 1-kHz signal frequency. Growth-of-masking functions were determined for each temporal condition, for a noise masker without a spectral notch. These functions were used to express the thresholds from the notched-noise experiment in terms of the level of a flat-spectrum noise which would produce the same threshold. In simultaneous masking the auditory filter shapes derived from the transformed data did not change significantly with signal delay, suggesting that the selectivity of the auditory filter does not develop over time. In forward masking the auditory filter shapes were sharper than those for simultaneous masking, particularly on the high-frequency side, which was attributed to suppression.     

Free-field release from masking

Free-field release from masking was studied as a function of the spatial separation of a signal and masker in a two-interval, forced-choice (2IFC) adaptive paradigm. The signal was a 250-ms train of clicks (100/s) generated by filtering 50-microseconds pulses with a TDH-49 speaker (0.9 to 9.0 kHz). The masker was continuous broadband (0.7 to 11 kHz) white noise presented at a level of 44 dBA measured at the position of the subject's head. In experiment I, masked and absolute thresholds were measured for 36 signal source locations (10 degree increments) along the horizontal plane as a function of seven masking source locations (30 degree increments). In experiment II, both absolute and masked thresholds were measured for seven signal locations along three vertical planes located at azimuthal rotations of 0 degrees (median vertical plane), 45 degrees, and 90 degrees. In experiment III, monaural absolute and masked thresholds were measured for various signal-masker configurations. Masking-level differences (MLDs) were computed relative to the condition where the signal and mask were in front of the subjects after using absolute thresholds to account for differences in the signal's sound-pressure level (SPL) due to direction. Maximum MLDs were 15 dB along the horizontal plane, 8 dB along the vertical, and 9 dB under monaural conditions.     

Effect of masker-frequency variability on the detection performance of infants and adults

The effect of masker-frequency variability on the detection performance of 7-9 month-old infants and adults was examined. Listeners detected a 300-ms 1000-Hz pure tone masked by: (1) A random-frequency two-tone complex; (2) a fixed-frequency two-tone complex; or (3) a broadband noise. Maskers repeated at 300-ms intervals throughout testing at 60 dB SPL. The signal was presented simultaneously with one presentation of the masker. Thresholds were determined adaptively using an observer-based method. Infants' thresholds were higher than adults' in all conditions, but infants' and adults' thresholds changed with masker condition in qualitatively similar ways. The fixed two-tone complex produced masking for both age groups, but more masking for infants than for adults. For infants and adults, the random two-tone complex produced more masking than broadband noise, but the difference was greater for infants than for adults. For infants and adults, the random two-tone complex produced more masking than the fixed two-tone complex, and the difference between these conditions was similar for both age groups. These results suggest that infants are more susceptible to informational masking than adults in the absence of spectral variability. Whether infants are more susceptible to the effects of masker-frequency variability than adults remains to be clarified.     

Forward masking: adaptation or integration?

The aim of this study was to attempt to distinguish between neural adaptation and persistence (or temporal integration) as possible explanations of forward masking. Thresholds were measured for a sinusoidal signal as a function of signal duration for conditions where the delay between the masker offset and the signal offset (the offset-offset interval) was fixed. The masker was a 200-ms broadband noise, presented at a spectrum level of 40 dB (re: 20 microPa), and the signal was a 4-kHz sinusoid, gated with 2-ms ramps. The offset-offset interval was fixed at various durations between 4 and 102 ms and signal thresholds were measured for a range of signal durations at each interval. A substantial decrease in thresholds was observed with increasing duration for signal durations up to about 20 ms. At short offset-offset intervals, the amount of temporal integration exceeded that normally found in quiet. The results were simulated using models of temporal integration (the temporal-window model) and adaptation. For both models, the inclusion of a peripheral nonlinearity, similar to that observed physiologically in studies of the basilar membrane, was essential in producing a good fit to the data. Both models were about equally successful in accounting for the present data. However, the temporal-window model provided a somewhat better account of similar data from a simultaneous-masking experiment, using the same parameters. This suggests that the linear, time-invariant properties of the temporal-window approach are appropriate for modeling forward masking. Overall the results confirm that forward masking can be described in terms of peripheral nonlinearity followed by linear temporal integration at higher levels in the auditory system. However, the difference in predictions between the adaptation and integration models is relatively small, meaning that influence of adaptation cannot be ruled out.     

Temporal integration in normal hearing, cochlear impairment, and impairment simulated by masking

To assess temporal integration in normal hearing, cochlear impairment, and impairment simulated by masking, absolute thresholds for tones were measured as a function of duration. Durations ranged from 500 ms down to 15 ms at 0.25 kHz, 8 ms at 1 kHz, and 2 ms at 4 and 14 kHz. An adaptive 2I, 2AFC procedure with feedback was used. On each trial, two 500-ms observation intervals, marked by lights, were presented with an interstimulus interval of 250 ms. The monaural signal was presented in the temporal center of one observation interval. The results for five normal and six impaired listeners show: (1) normal listeners' thresholds decrease by about 8 to 10 dB per decade of duration, as expected; (2) listeners with cochlear impairments generally show less temporal integration than normal listeners; and (3) listeners with impairments simulated using masking noise generally show the same amount of temporal integration as normal listeners tested in the quiet. The difference between real and simulated impairments indicates that the reduced temporal integration observed in impaired listeners probably is not due to splatter of energy to frequency regions where thresholds are low, but reflects reduced temporal integration per se.     

High-frequency auditory filter shape for the Atlantic bottlenose dolphin

High-frequency auditory filter shapes of an Atlantic bottlenose dolphin (Tursiops truncatus) were measured using a notched noise masking source centered on pure tone signals at frequencies of 40, 60, 80 and 100?kHz. A dolphin was trained to swim into a hoop station facing the noise/signal transducer located at a distance of 2?m. The dolphin's masked threshold was determined using an up-down staircase method as the width of the notched noise was randomly varied from 0, 0.2, 04, 0.6, and 0.8 times the test tone frequency. The masked threshold decreased as the width of the notched increased and less noise fell within the auditory filter associated with the test tone. The auditory filter shapes were approximated by fitting a roex (p,r(r)) function to the masked threshold results. A constant-Q value of 8.4 modeled the results within the frequency range of 40 to 100 kHz relatively well. However, between 60 and 100?kHz, the 3?dB bandwidth was relatively similar between 9.5 and 10?kHz, indicating a constant-bandwidth system in this frequency range The mean equivalent rectangular bandwidth calculated from the filter shape was approximately 16.0%, 17.0%, 13.6% and 11.3% of the tone frequencies of 40, 60, 80, and 100?kHz.     

Detection of intensity decrements by the chinchilla.

Three monaural chinchillas were trained to detect intensity decrements in broadband noise (20 kHz) using a shock-avoidance conditioning procedure. The intensity decrements were presented at one of nine different durations between 2 and 35 ms at noise levels of 25, 45, and 65 dB SPL. At each intensity-duration combination, the level of the decrement was varied to obtain a decrement threshold. The minimal detectable decrement decreased from approximately 20 dB at the shortest duration to an asymptote of roughly 4 dB at approximately 30 ms. The data were modeled by a low-pass filter with an 11-ms time constant. The decrement detection function of the chinchilla is similar to that of humans. However, long-duration decrement thresholds are larger in the chinchilla, as would be predicted from the large intensity difference limen of the chinchilla. In general, there was little change in the decrement function across background intensities except that 2-ms decrements were not detected at the 25-dB SPL background intensity.     

The effect of pure-tone forward masking on overshoot

The overshoot effect can be reduced by temporary hearing loss induced by aspirin or exposure to intense sound. The present study simulated a hearing loss at 4.0 kHz via pure-tone forward masking and examined the effect of the simulation on threshold for a 10-ms, 4.0-kHz signal presented 1 ms after the onset of a 400-ms, broadband noise masker whose spectrum level was 20 dB SPL. Masker frequency was 3.6, 4.0, or 4.2 kHz, and masker level was 80 dB SPL. Subject-dependent delays were determined such that 10 or 20 dB of masking at 4.0 kHz was produced. In general, the pure-tone forward masker did not reduce the simultaneous-masked threshold, suggesting that elevating threshold with a pure-tone forward masker does not sufficiently simulate the effect of a temporary hearing loss on overshoot.     

Effects of masker-spectral variability and masker fringes in children and adults

This study examined the degree to which masker-spectral variability contributes to children's susceptibility to informational masking. Listeners were younger children (5-7 years), older children (8-10 years), and adults (19-34 years). Masked thresholds were measured using a 2IFC, adaptive procedure for a 300-ms, 1000-Hz signal presented simultaneously with (1) broadband noise, (2) a random-frequency ten-tone complex, or (3) a fixed-frequency ten-tone complex. Maskers were presented at an overall level of 60 dB SPL. Thresholds were similar across age for the noise condition. Thresholds for most children were higher than for most adults, however, for both ten-tone conditions. The average difference in threshold between random and fixed ten-tone conditions was comparable across age, suggesting a similar effect of reducing masker-spectral variability in children and adults. Children appear more likely to be susceptible to informational masking than adults, however, both with and in the absence of masker-spectral variability. The addition of a masker fringe (delayed onset of signal relative to masker) provided a release from masking for fixed and random ten-tone conditions in all age groups, suggesting at least part of the masking observed for both ten-tone maskers was informational.     

On the growth of masking asymmetry with stimulus intensity

Masking asymmetry was investigated over a wide range of stimulus intensities for two signal frequencies, fo = 1.0 and 4.0 kHz, using both fixed-masker and fixed-signal paradigms. The masker was a notched noise with the upper and lower edges of the notch, fu and fl, respectively, placed asymmetrically about fo. For various notch widths, the asymmetry of masking was measured as the difference between the masked threshold obtained when fl was nearer fo and that obtained when fu was nearer fo. For maskers with wide notches, (fu - fl)/fo greater than 0.15, masking asymmetry changed with stimulus level; at the highest level, masked threshold was greatest when fl was nearer fo, and, at the lowest level the asymmetry reversed slightly for fo = 1.0 kHz so that masked threshold was actually greater when fu was nearer fo. Nonparallel growth of masking functions reveal changes in masking asymmetry with signal level as well as with masker level. It is concluded that the nonlinear growth of masking with level is due primarily to changes in the auditory filter, rather than changes in the detector following the filter.     

Effects of non-simultaneous masking on the binaural masking level difference

The present study sought to clarify the role of non-simultaneous masking in the binaural masking level difference for maskers that fluctuate in level. In the first experiment the signal was a brief 500-Hz tone, and the masker was a bandpass noise (100-2000 Hz), with the initial and final 200-ms bursts presented at 40-dB spectrum level and the inter-burst gap presented at 20-dB spectrum level. Temporal windows were fitted to thresholds measured for a range of gap durations and signal positions within the gap. In the second experiment, individual differences in out of phase (NoSπ) thresholds were compared for a brief signal in a gapped bandpass masker, a brief signal in a steady bandpass masker, and a long signal in a narrowband (50-Hz-wide) noise masker. The third experiment measured brief tone detection thresholds in forward, simultaneous, and backward masking conditions for a 50- and for a 1900-Hz-wide noise masker centered on the 500-Hz signal frequency. Results are consistent with comparable temporal resolution in the in phase (NoSo) and NoSπ conditions and no effect of temporal resolution on individual observers' ability to utilize binaural cues in narrowband noise. The large masking release observed for a narrowband noise masker may be due to binaural masking release from non-simultaneous, informational masking.     

Vibrotactile masking: effects of stimulus onset asynchrony and stimulus frequency

Vibrotactile thresholds for the detection of a 50-ms vibratory stimulus on the thenar eminence of the hand were measured in the presence of and in the absence of a 700-ms suprathreshold vibratory masking stimulus. When thresholds were measured in the presence of the masking stimulus, stimulus onset asynchrony (SOA) was varied so that backward, simultaneous, and forward masking could be measured. The amount of masking, expressed as threshold shift, was greatest when the test stimulus was presented near the onset or offset of the masking stimulus. For both backward and forward masking, the amount of masking decreased as a function of increasing stimulus onset asynchrony. Comparisons were made of the amounts of masking measured when the test and masking stimuli were both sinusoids, and when the test stimulus was a sinusoid and the masking stimulus was noise. In all conditions, the masked threshold decreased approximately 4.0 dB when SOA was increased from 100 to 650 ms with reference to the onset of the 700-ms masking stimulus. More simultaneous masking was observed when sinusoidal test stimuli were detected in the presence of noise than when they were detected in the presence of sinusoidal maskers of the same frequency. The functions were essentially identical for detection of a low-frequency (20 Hz) test stimulus mediated by a non-Pacinian channel and detection of a high-frequency (250 Hz) test stimulus mediated by the Pacinian channel.     

Behavioral measures of frequency selectivity in the chinchilla.

A simultaneous masking procedure was used to derive four measures of frequency selectivity in the chinchilla. The first experiment measured critical masking ratios (CRs) at various signal frequencies. Estimates of the chinchillas' critical bandwidths derived from the CRs were much broader than comparable human estimates, indicating that the chinchilla may have inferior frequency selectivity. The second experiment measured critical bandwidths at 1, 2, and 4 kHz in a band-narrowing experiment. This technique yielded narrower estimates of critical bandwidth; however, chinchillas continued to exhibit poor frequency selectivity compared to man. The third experiment measured auditory-filter shape at 0.5, 1, and 2 kHz via rippled noise masking. Results of the rippled noise masking experiment indicate that auditory filters of humans and chinchillas are similar in terms of shape and bandwidth with chinchillas showing only slightly poorer frequency selectivity. The final experiment measured auditory filter shape at 0.5, 1, 2, and 4 kHz using notched noise masking. This experiment yielded auditory filter shapes and bandwidths similar to those derived from man. The discrepancy between the indirect estimates of frequency selectivity derived from CR and band-narrowing techniques and the direct estimates derived from rippled noise and notched noise masking are explained by taking into account the processing efficiency of the subjects.     

The effect of masker spectral asymmetry on overshoot in simultaneous masking

"Overshoot" is a simultaneous masking phenomenon: Thresholds for short high-frequency tone bursts presented shortly after the onset of a broadband masker are raised compared to thresholds in the presence of a continuous masker. Overshoot for 2-ms bursts of a 5000-Hz test tone is described for four subjects as a function of the spectral composition and level of the masker. First, it was verified that overshoot is largely independent of masker duration. Second, overshoot was determined for a variety of 10-ms masker bursts composed of differently filtered uniform masking noise with an overall level of 60 dB SPL: unfiltered, high-pass (cutoff at 3700 Hz), low-pass (cutoff at 5700 Hz), and third-octave-band-(centered at 5000 Hz) filtered uniform masking noises presented separately or combined with different bandpass maskers (5700-16000 Hz, 5700-9500 Hz, 8400-16000 Hz) were used. Third, masked thresholds were measured for maskers composed of an upper or lower octave band adjacent to the third-octave-band masker as a function of the level of the octave band. All maskers containing components above the critical band of the test tone led to overshoot; no additional overshoot was produced by masker components below it. Typical values of overshoot were on the order of 12 dB. Overshoot saturated when masker levels were above 60 dB SPL for the upper octave-band masker. The standard neurophysiological explanation of overshoot accounts only partially for these data. Details that must be accommodated by any full explanation of overshoot are discussed.     

Age differences in backward masking

The present study was designed to assess the effects of age on the time course of backward masking. In experiment 1, thresholds for detecting a 10-ms, 500-Hz sinusoidal signal were measured as a function of the temporal separation between the signal and a 50-ms broadband masker. Subjects were younger (18-24) and older (over age 65) adults with normal hearing (thresholds less than 20 dB HL) for frequencies of 4 kHz and below. Younger subjects exhibited less overall masking and steeper recovery functions than did the older adults. Masked thresholds for younger participants approached unmasked thresholds for signal-masker delays greater than 6-8 ms. In contrast, older adults exhibited significant masking even at the longest delay tested (20 ms). In experiment 2, signal duration was decreased to 5 ms for a separate group of younger adults. Although overall thresholds were elevated for the shorter signal duration, the slope of the backward masking recovery function was not different from that observed for younger adults in experiment 1. The results suggest that age, independent of hearing loss, affects the temporal course of backward masking.     

Temporal effects in masking and their influence on psychophysical tuning curves

Psychophysical tuning curves (PTCs) were obtained in simultaneous and forward masking for a 20-ms, 1000-Hz signal presented at 10 dB SL. The signal was presented at the beginning of, at the temporal center of, at the end of, or immediately following a 400-ms masker. The first experiment was done in quiet; the second experiment was done in the presence of two bands of noise on either side of 1000 Hz. The results were similar in quiet and in noise. In simultaneous masking, the PTCs were broadest for the signal at masker onset, and generally sharpest for the signal at temporal center; the differences were largest on the high-frequency side. In most cases, there was virtually no difference in Q10 between the forward-masking PTC and the simultaneous-masking PTC with the signal temporally centered, although the high-frequency slope was always steeper in forward masking. These results indicate that, at least for brief signals, frequency selectivity measured with simultaneous-masking PTCs and the degree of sharpening revealed in forward-masking PTCs depend upon the temporal position of the signal within the simultaneous masker.