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B C Moore

Publications and source records attributed to B C Moore.

At least 37 records · Page 2Linked to original sources

Effects of relative phase and frequency spacing on the detection of three-component amplitude modulation.

These experiments explored the effect of relative modulator phase on the detection of a three-component modulator applied to a 4,000-Hz sinusoidal carrier with a level of 70 dB SPL. The central modulator component had a frequency of 50 Hz, and the two other components had frequencies of 50+/-5, 10, 25, 40, or 45 Hz. Thus, the modulator waveform was always periodic. Each modulator component had the same modulation index, m. The relative phases of the components were chosen to give a variety of modulation waveforms differing in the ratio of maximum to minimum value (max-min) and in crest factor. In experiment 1, modulation detection thresholds were measured by varying m, using an adaptive two-interval forced-choice procedure. Thresholds were found to be independent of relative modulator phase and of the frequency spacing of the components. In experiment 2, detectability (d') of the modulation was measured for several fixed values of m. Detectability was found to be independent of relative modulator phase and of the frequency spacing of the components. The results are not consistent with the idea that modulation detection thresholds are determined by the max-min value or crest factor of the envelope. The results are consistent with a model which assumes that the stimuli are subjected to a nonlinearity, and thresholds are determined by the root-mean-square value (or the mean square value) of the ac component of the envelope, following this nonlinearity. The nonlinearity may partly reflect compression on the basilar membrane, but other nonlinearities may be involved. This model can also explain some aspects of earlier results on the sensitivity to relative modulator phase [E. A. Strickland and N. F. Viemeister, J. Acoust. Soc. Am. 99, 3638-3646 (1996)].

Auditory Threshold↗

Frequency selectivity as a function of level and frequency measured with uniformly exciting notched noise.

Thresholds for detecting sinusoidal signals were measured as a function of the spectral width of a notch in a noise masker. The notch was positioned both symmetrically and asymmetrically around the signal frequency. The noise was designed to create equal excitation per ERB within its passbands (uniformly exciting noise), after allowing for the transfer function of the headphone and the middle ear. For a signal frequency of 250 Hz, the level per ERB ranged from 35 to 80 dB in 15-dB steps. For signal frequencies of 500, 1,000, 2,000, and 4,000 Hz, the level per ERB ranged from 40 to 70 dB per ERB in 15-dB steps. Auditory filter shapes were derived from the data by modeling the auditory filter as the sum of a sharply tuned tip filter and a broader tail filter. The gain of the tip filter was assumed to be a function of level. The shape of the tip filter and the gain and shape of the tail filter were assumed to be level independent. The data for all levels were fitted simultaneously. The data were fitted best when the gain of the tip filter was assumed to be a function of the signal level (as opposed to the masker level per ERB). The filter shapes showed a level dependence that qualitatively resembled the level dependence of filtering on the basilar membrane. The maximum gain of the tip filter tended to increase with increasing center frequency up to 1 kHz, but to remain roughly constant for higher frequencies.

Adult↗

Detection of quasitrapezoidal frequency and amplitude modulation.

It has been proposed that the detection of frequency modulation (FM) of sinusoidal carriers can be mediated by two mechanisms; a place mechanism based on FM-induced amplitude modulation (AM) in the excitation pattern, and a temporal mechanism based on phase locking in the auditory nerve. The temporal mechanism appears to be "sluggish" and does not play a role for FM rates above about 10 Hz. It also does not play a role for high carrier frequencies (above about 5 kHz). This experiment provided a further test of the hypothesis that the effectiveness of the temporal mechanism depends upon the time spent close to frequency extremes during the modulation cycle. Psychometric functions for the detection of AM and FM were measured for two carrier frequencies, 1 and 6 kHz. The modulation waveform was quasitrapezoidal. Within each modulation period, P, a time Tss was spent at each extreme of frequency or amplitude. The transitions between the extremes, with duration Ttrans had the form of a half-cycle of a cosine function. The modulation rate was 2, 5, 10, or 20 Hz, giving values of P of 500, 200, 100, and 50 ms. TSS varied from 0 ms (sinusoidal modulation) up to 160, 80, 40, or 20 ms, for rates of 2, 5, 10, and 20 Hz, respectively. The detectability of AM was not greatly affected by modulation rate or by the value of TSS, except for a slight improvement with increasing TSS for the lowest modulation rates; this was true for both carrier frequencies. For FM of the 6-kHz carrier, the pattern of results was similar to that found for AM, which is consistent with an excitation-pattern model of FM detection. For FM of the 1-kHz carrier, performance improved markedly with increasing TSS, especially for the lower FM rates; there was no change in performance with TSS for the 20-Hz modulation rate. The results are consistent with the idea that detection of FM of a 1-kHz carrier is partly mediated by a sluggish temporal mechanism. That mechanism benefits from greater time spent at frequency extremes of the modulation cycle for rates up to 10 Hz.

Auditory Perception↗

The effect of modulation rate on the detection of frequency modulation and mistuning of complex tones.

Experiment 1 measured frequency modulation detection thresholds (FMTs) for harmonic complex tones as a function of modulation rate. Six complexes were used, with fundamental frequencies (F0s) of either 88 or 250 Hz, bandpass filtered into a LOW (125-625 Hz), MID (1375-1875 Hz) or HIGH (3900-5400 Hz) frequency region. The FMTs were about an order of magnitude greater for the three complexes whose harmonics were unresolved by the peripheral auditory system (F0 = 88 Hz in the MID region and both F0s in the HIGH region) than for the other three complexes, which contained some resolved harmonics. Thresholds increased with increases in FM rate above 2 Hz for all conditions. The increase was larger when the F0 was 88 Hz than when it was 250 Hz, and was also larger in the LOW than in the MID and HIGH regions. Experiment 2 measured thresholds for detecting mistuning produced by modulating the F0s of two simultaneously presented complexes out of phase by 180 degrees. The size of the resulting mistuning oscillates at a rate equal to the rate of FM applied to the two carriers. At low FM rates, thresholds were lowest when the harmonics were either resolved for both complexes or unresolved for both complexes, and highest when resolvability differed across complexes. For pairs of complexes with resolved harmonics, mistuning thresholds increased dramatically as the FM rate was increased above 2-5 Hz, in a way which could not be accounted for by the effect of modulation rate on the FMTs for the individual complexes. A third experiment, in which listeners detected constant ("static") mistuning between pairs of frequency-modulated complexes, provided evidence that this deterioration was due the harmonics in one of the two "resolved" complexes becoming unresolved at high FM rates, when analyzed over some finite time window. It is concluded that the detection of time-varying mistuning between groups of harmonics is limited by factors that are not apparent in FM detection data.

Adult↗

COX-2 inhibition, apoptosis, and chemoprevention by nonsteroidal anti-inflammatory drugs.

Non-steroidal anti-inflammatory drugs (NSAIDs) have as their common mechanism the inhibition of cyclooxygenase (COX) enzymes, of which two isoforms (COX-1 and COX-2) exist. The effect of NSAIDs on chemoprevention and tumor regression has been shown in animal models, epidemiologic studies, and in treatment of patients. The exact biochemical and cellular mechanisms underlying each of these phenomena is only partially understood. Processes that have been recently implicated as being important include the inhibition of tumor cell growth, prevention of angiogenesis, and induction of apoptosis in neoplastic cells.

Animals↗

Comparison of the NAL(R) and Cambridge formulae for the fitting of linear hearing aids.

This paper describes a laboratory-based comparison of the effectiveness of two formulae for fitting linear hearing aids, the NAL(R) formula and the Cambridge formula. The formulae prescribe the desired insertion gain as a function of frequency, based on the audiometric threshold. The two formulae have a similar rationale; both are based on the goal that, for speech with a moderate level, all frequency bands should be equally loud (equal loudness per critical band) over the frequency range important for speech (400-5000 Hz), and the overall loudness should be comfortable. However, the formulae differ; generally the Cambridge formula leads to slightly more high-frequency gain (above 2 kHz) and slightly less mid-frequency gain (between 500 Hz and 2000 Hz) than the NAL(R) formula. The two formulae were implemented using an experimental digital hearing aid whose frequency-gain characteristic could be controlled very precisely. A loudness model (Moore and Glasberg, 1997) was used to adjust the overall gains for each subject and each formula so that a speech-shaped noise with an overall level of 65 dB SPL would give the same loudness as for a normally hearing person (according to the model). The adjustments were, on average, smaller for the Cambridge than for the NAL(R) formula. A condition was also used with all insertion gains set to zero, simulating unaided listening. Evaluation was based on: (1) subjective ratings of the loudness, intelligibility and quality of continuous discourse presented in quiet at levels of 45, 55, 65 and 75 dB SPL and in babble at an 0-dB speech-to-babble ratio, using speech levels of 55, 65 and 75 dB SPL; (2) measures of the speech reception threshold (SRT) in background noise for two noise levels (65 and 75 dB SPL) and four types of background noise. Neither the subjective ratings nor the measures of the SRTs revealed any consistent difference between the results obtained using the two formulae, although both formulae led to lower (better) SRTs than for simulated unaided listening. It is concluded that the differences between the NAL(R) formula and the Cambridge formula are too small to have measurable effects, at least in a laboratory setting.

Aged↗

Use of a loudness model for hearing aid fitting. IV. Fitting hearing aids with multi-channel compression so as to restore 'normal' loudness for speech at different levels.

Many researchers have proposed that multi-channel compression hearing aids should process sounds so as to restore loudness perception to 'normal'. However, procedures for achieving this have generally been based on measurements or calculations using narrowband stimuli, and these procedures may not be accurate for broadband sounds such as speech. Here, a model for predicting loudness for people with cochlear hearing loss is used to calculate the frequency- and level-dependent gains that would be required to restore loudness perception to 'normal' for speech-like signals. The calculations are based entirely on the pure tone audiogram, and do not require measures of loudness growth. The model was applied to several different hypothetical hearing losses, varying in slope and severity. In each case, the model was used to calculate the insertion gains (IGs) that would be required as a function of frequency so that speech-shaped noise with a level of 65 dB SPL would evoke a specific loudness pattern matching that for a normal ear. A similar procedure was applied using speech-shaped noise with a level of 85 dB SPL (with the spectral characteristics of shouted speech). The results were used to derive functions relating the required IG to hearing loss for each audiometric frequency and each speech-shaped noise level. These functions were used in turn to derive compression ratios and gains for each channel of a multi-channel compression system. The derivations apply to systems with any number of channels. The outcome is a method than can be used for the initial fitting of multichannel compression hearing aids, so as to restore loudness perception to near 'normal' for broadband speech-like signals.

Acoustic Stimulation↗

A test for the diagnosis of dead regions in the cochlea.

Hearing impairment may sometimes be associated with complete loss of inner hair cells (IHCs) over a certain region of the basilar membrane. We call this a 'dead region'. Amplification (using a hearing aid) over a frequency range corresponding to a dead region may not be beneficial and may even impair speech intelligibility. However, diagnosis of dead regions is not easily done from the audiogram. This paper reports the design and evaluation of a method for detecting and delimiting dead regions. A noise, called 'threshold equalizing noise' (TEN), was spectrally shaped so that, for normally hearing subjects, it would give equal masked thresholds for pure tone signals at all frequencies within the range 250-10,000 Hz. Its level is specified as the level in a one-ERB (132 Hz) wide band centred at 1000 Hz. Measurements obtained from 22 normal-hearing subjects and TEN levels of 30, 50 and 70 dB/ERB confirmed that the signal level at masked threshold was approximately equal to the noise level/ERB and was almost independent of signal frequency. Masked thresholds were measured for 20 ears of 14 subjects with sensorineural hearing loss, using TEN levels of 30, 50 and 70 dB/ERB. Psychophysical tuning curves (PTCs) were measured for the same subjects. When there are surviving IHCs corresponding to a frequency region with elevated absolute thresholds, a signal in that frequency region is detected via IHCs with characteristic frequencies (CFs) close to that region. In such a case, threshold in the TEN is close to that for normal-hearing listeners, provided that the noise intensity is sufficient to produce significant masking. Also, the tip of the PTC lies close to the signal frequency. When a dead region is present, the signal is detected via IHCs with CFs different from that of the signal frequency. In such a case, threshold in the TEN is markedly higher than normal, and the tip of the PTC is shifted away from the signal frequency. Generally, there was a very good correspondence between the results obtained using the TEN and the PTCs. We conclude that the measurement of masked thresholds in TEN provides a quick and simple method for the diagnosis of dead regions.

Aged↗

Tolerable hearing aid delays. I. Estimation of limits imposed by the auditory path alone using simulated hearing losses.

OBJECTIVE: When people who wear hearing aids speak, there are three paths by which they hear their own voices: 1) through the air and leakage around the earmold; 2) via the solid structures of their head; 3) through the air to the hearing aid microphone, and then through the aid circuitry. These paths involve different time delays. Digital processing introduces delays in path 3 from a few to several tens of milliseconds, which could lead to a range of disturbing effects. We examined one purely auditory effect, namely hearing speech through all three of these paths. Subjective disturbance was measured as a function of delay in path 3 using simulations of hearing loss and a simulated hearing aid. With increasing hearing loss, the loudness of sound heard via paths 1 and 2 decreases, and the aid user relies more on path 3. The disturbance produced by the delay then might be less perceptible. To test this idea, four different hearing losses were simulated, varying from mild to moderately severe. DESIGN: Each of two talkers was fitted with a closed earmold, and simultaneous above-ear and in-ear recordings were made of each talker reading prose. The above-ear signal was amplified using a simulated hearing aid with 4-channel full dynamic range compression; compression ratios and gains were selected using an algorithm based on the absolute thresholds used in the simulations of hearing loss. The resultant output was then mixed with the in-ear signal with one of five values of delay, and the combined signal was processed using the four simulations of hearing loss. The resulting stimuli simulated for normal-hearing listeners the experience of having a hearing impairment and listening through a hearing aid while talking, except that the talker's voice was not that of the listener. Twenty normally hearing subjects gave subjective ratings of the disturbance of the echo for each delay and each simulated hearing loss. RESULTS: Disturbance ratings generally increased monotonically with increasing delay. Average results show that delays are rated as "disturbing" for values between 20 and 30 msec for mild to moderate losses. For a moderately severe loss, the rating "disturbing" was not quite achieved at 40 msec. For moderate losses, a speaker with low fundamental frequency (f0)(70 to 140 Hz) was less disturbing than a speaker with a medium f0, (100 to 180 Hz). This effect reversed for the mildest loss for low values of delay. CONCLUSIONS: The auditory effects of delays between bone-conducted sound and aid-conducted sound are likely to become disturbing for delays exceeding 20 msec. Somewhat longer delays may be tolerable for moderate to severe hearing losses. These delays are smaller than the delays at which audio-visual integration is disrupted.

Adult↗

Benefits of linear amplification and multichannel compression for speech comprehension in backgrounds with spectral and temporal dips.

People with cochlear hearing loss have markedly higher speech-receptions thresholds (SRTs) than normal for speech presented in background sounds with spectral and/or temporal dips. This article examines the extent to which SRTs can be improved by linear amplification with appropriate frequency-response shaping, and by fast-acting wide-dynamic-range compression amplification with one, two, four, or eight channels. Eighteen elderly subjects with moderate to severe hearing loss were tested. SRTs for sentences were measured for four background sounds, presented at a nominal level (prior to amplification) of 65 dB SPL: (1) A single female talker, digitally filtered so that the long-term average spectrum matched that of the target speech; (2) a noise with the same average spectrum as the target speech, but with the temporal envelope of the single talker; (3) a noise with the same overall spectral shape as the target speech, but filtered so as to have 4 equivalent-rectangular-bandwidth (ERB) wide spectral notches at several frequencies; (4) a noise with both spectral and temporal dips obtained by applying the temporal envelope of a single talker to speech-shaped noise [as in (2)] and then filtering that noise [as in (3)]. Mean SRTs were 5-6 dB lower (better) in all of the conditions with amplification than for unaided listening. SRTs were significantly lower for the systems with one-, four-, and eight-channel compression than for linear amplification, although the benefit, averaged across subjects, was typically only 0.5 to 0.9 dB. The lowest mean SRT (-9.9 dB, expressed as a speech-to-background ratio) was obtained for noise (4) and the system with eight-channel compression. This is about 6 dB worse than for elderly subjects with near-normal hearing, when tested without amplification. It is concluded that amplification, and especially fast-acting compression amplification, can improve the ability to understand speech in background sounds with spectral and temporal dips, but it does not restore performance to normal.

Aged↗

Factors affecting the loudness of modulated sounds.

Loudness matches were obtained between unmodulated carriers and carriers that were amplitude modulated either periodically (rates between 2 and 32 Hz, modulation sinusoidal either on a linear amplitude scale or on a dB scale; the latter is called dB modulation) or with the envelope of the speech of a single talker. The carrier was a 4-kHz sinusoid, white noise, or speech-shaped noise. Both normally hearing subjects and subjects with cochlear hearing loss were tested. Results were expressed as the root-mean-square (rms) level of the modulated carrier minus the level of the unmodulated carrier at the point of equal loudness. If this difference is positive, this indicates that the modulated carrier has a higher rms level at the point of equal loudness. For normally hearing subjects, the results show: (1) For a 4000-Hz sinusoidal carrier, the difference was slightly positive (averaging about 0.7 dB). There was no significant effect of modulation rate or level over the range 20-80 dB SL. (2) For a speech-shaped noise or white noise carrier, the difference was close to zero, although for large modulation depths it tended to be negative. There was no clear effect of level (over the range 35-75 dB SPL) or modulation rate. For the hearing-impaired subjects, the differences were small, but tended to be slightly negative for both the 4000-Hz carrier and the noise carriers, when the modulation rate was above 2 Hz. Again, there was no clear effect of overall level. However, for dB modulation, the differences became more negative with increasing modulation depth. For modulation rates in the range 4-32 Hz, the results could be fitted reasonably well using the assumption that the loudness of modulated sounds is based on the rms value of the time-varying intensity of the response of the basilar membrane (taking into account the compression that occurs in the normal cochlea). The implications of the results for the fitting of multi-band compression hearing aids and for the design of loudness meters are discussed.

Adult↗

Discrimination of frequency steps linked by glides of various durations.

Thresholds were measured for detecting steps in frequency linked by glides of various durations. The goals were to assess the relative importance of place and temporal information for this task, and to determine whether there is a mechanism for detecting dynamic frequency changes per se, as opposed to comparing the initial and final frequencies of the stimuli. Subjects discriminated a 500-ms sinusoid of constant frequency from a sinusoid with three parts: an initial part with constant frequency, a downward frequency glide, and a final part with constant frequency. The overall duration was 500 ms, and the glide duration was varied from 5 to 500 ms. In one special case, the portion of the stimuli when a glide might occur was replaced by a brief silent interval. The center frequency was fixed at 0.5, 1, 2, 4, or 6 kHz (condition 1), or varied randomly from one stimulus to the next over a 4-ERB range around the nominal center frequency (condition 2). The randomization impaired performance, but thresholds remained lower than the best that could be achieved by monitoring either the initial or final frequency of the stimuli. Condition 3 was like condition 2, but for each stimulus a glide in level was added at the time when a frequency glide might occur, so the initial and final levels differed; the glides in level varied randomly in extent and direction from one stimulus to the next over the range +/- 20 dB. This impaired performance, but thresholds remained lower than the best that could be achieved by monitoring changes in excitation level on only one side of the excitation pattern. Excitation-pattern models of frequency discrimination predict that thresholds should not vary across center frequency when expressed as the change in ERB number, delta E. For all conditions, delta E values increased at 6 kHz, suggesting a role for temporal information at lower frequencies. The increase was smallest for the longest glide duration, consistent with a greater relative role of place information when there was no steady state portion. Performance was better when a brief glide was present than when no glide was present, but worsened with increasing glide duration. The results were fitted well by a model based on the assumption that information from the steady parts of the stimuli (perhaps extracted mainly using temporal information) was combined with information from the glides (perhaps extracted mainly using place information).

Auditory Threshold↗

Further evaluation of a model of loudness perception applied to cochlear hearing loss.

This paper describes further tests of a model for loudness perception in people with cochlear hearing loss. It is assumed that the hearing loss (the elevation in absolute threshold) at each audiometric frequency can be partitioned into a loss due to damage to outer hair cells (OHCs) and a loss due to damage to inner hair cells (IHCs) and/or neurons. The former affects primarily the active mechanism that amplifies the basilar membrane (BM) response to weak sounds. It is modeled by increasing the excitation level required for threshold, which results in a steeper growth of specific loudness with increasing excitation level. Loss of frequency selectivity, which results in broader excitation patterns, is also assumed to be directly related to the OHC loss. IHC damage is modeled by an attenuation of the calculated excitation level at each frequency. The model also allows for the possibility of complete loss of IHCs or functional neurons at certain places within the cochlea ("dead" regions). The parameters of the model (OHC loss at each audiometric frequency, plus frequency limits of the dead regions) were determined for three subjects with unilateral cochlear hearing loss, using data on loudness matches between sinusoids presented alternately to their two ears. Further experiments used bands of noise that were either 1-equivalent rectangular bandwidth (ERB) wide or 6-ERBs wide, centered at 1 kHz. Subjects made loudness matches for these bands of noise both within ears and across ears. The model was reasonably accurate in predicting the results of these matches without any further adjustment of the parameters.

Audiometry, Pure-Tone↗

Modulation masking produced by beating modulators.

This study examined whether "modulation masking" could be produced by temporal similarity of the probe and masker envelopes, even when the masker envelope did not contain a spectral component close to the probe frequency. Both masker and probe amplitude modulation were applied to a single 4-kHz sinusoidal or narrow-band noise carrier with a level of 70 dB SPL. The threshold for detecting 5-Hz probe modulation was affected by the presence of a pair of masker modulators beating at a 5-Hz rate (40 and 45 Hz, 50 and 55 Hz, or 60 and 65 Hz). The threshold was dependent on the phase of the probe modulation relative to the beat cycle of the masker modulators; the threshold elevation was greatest (12-15 dB for the sinusoidal carrier and 9-11 dB for the noise carrier, expressed as 20 log m) when the peak amplitude of the probe modulation coincided with a peak in the beat cycle. The maximum threshold elevation of the 5-Hz probe produced by the beating masker modulators was 7-12 dB greater than that produced by the individual components of the masker modulators. The threshold elevation produced by the beating masker modulators was 2-10 dB greater for 5-Hz probe modulation than for 3- or 7-Hz probe modulation. These results cannot be explained in terms of the spectra of the envelopes of the stimuli, as the beating masker modulators did not produce a 5-Hz component in the spectra of the envelopes. The threshold for detecting 5-Hz probe modulation in the presence of 5-Hz masker modulation varied with the relative phase of the probe and masker modulation. The pattern of results was similar to that found with the beating two-component modulators, except that thresholds were highest when the masker and probe were 180 degrees out of phase. The results are consistent with the idea that nonlinearities within the auditory system introduce distortion in the internal representation of the envelopes of the stimuli. In the case of two-component beating modulators, a weak component is introduced at the beat rate, and it has an amplitude minimum when the beat cycle is at its maximum. The results could be fitted well using two models, one based on the concept of a sliding temporal integrator and one based on the concept of a modulation filter bank.

Auditory Perception↗

The role of spectral and periodicity cues in auditory stream segregation, measured using a temporal discrimination task.

In a previous paper, it was shown that sequential stream segregation could be based on both spectral information and periodicity information, if listeners were encouraged to hear segregation [Vliegen and Oxenham, J. Acoust. Soc. Am. 105, 339-346 (1999)]. The present paper investigates whether segregation based on periodicity information alone also occurs when the task requires integration. This addresses the question: Is segregation based on periodicity automatic and obligatory? A temporal discrimination task was used, as there is evidence that it is difficult to compare the timing of auditory events that are perceived as being in different perceptual streams. An ABA ABA ABA... sequence was used, in which tone B could be either exactly at the temporal midpoint between two successive tones A or slightly delayed. The tones A and B were of three types: (1) both pure tones; (2) both complex tones filtered through a fixed passband so as to contain only harmonics higher than the 10th, thereby eliminating detectable spectral differences, where only the fundamental frequency (f0) was varied between tones A and B; and (3) both complex tones with the same f0, but where the center frequency of the spectral passband varied between tones. Tone A had a fixed frequency of 300 Hz (when A and B were pure tones) or a fundamental frequency (f0) of 100 Hz (when A and B were complex tones). Five different intervals, ranging from 1 to 18 semitones, were used. The results for all three conditions showed that shift thresholds increased with increasing interval between tones A and B, but the effect was largest for the conditions where A and B differed in spectrum (i.e., the pure-tone and the variable-center-frequency conditions). The results suggest that spectral information is dominant in inducing (involuntary) segregation, but periodicity information can also play a role.

Adolescent↗

Detection and intensity discrimination of Gaussian-shaped tone pulses as a function of duration.

Van Schijndel et al. [J. Acoust. Soc. Am. 105, 3425-3435 (1999)] proposed that the auditory system partitions the spectro-temporal domain into frequency-time (f-t) windows and that the characteristics of these windows could be explored by measuring intensity discrimination for Gaussian-shaped tone pulses presented just above their detection threshold in noise. They reasoned that for a long-duration tone pulse, the auditory representation would be maximally compact in the frequency domain, but would spread across several f-t windows in the time domain. For a very-short-duration tone pulse, the auditory representation would be maximally compact in the time domain, but would spread across several f-t windows in the frequency domain. There should be some intermediate duration at which the auditory representation is compact in both the time and frequency domains and for which intensity-discrimination performance should worsen, due to the limited opportunity for multiple looks. Their data for signal frequencies of 1 and 4 kHz were consistent with this expectation; intensity discrimination was poorest at a duration of about 3-5 ms at 1 kHz and 1 ms at 4 kHz (durations are specified between 6.8-dB-down points on the envelope). This experiment attempted to replicate those results and to extend them to a wider range of frequencies and levels. Intensity discrimination of Gaussian-shaped tone pulses was measured at three levels: 10 dB above absolute threshold or above masked threshold in a pink noise with a spectrum level of either 15 or 40 dB at 1 kHz. The signal frequency was 0.25 kHz (durations from 2 to 320 ms), 1 kHz (durations from 0.5 to 80 ms), or 4 kHz (durations from 0.1 to 20 ms). Three normally hearing subjects were tested. At 1 and 4 kHz, performance was poorest overall for the 15-dB pink noise level, and thresholds showed a peak at intermediate durations (about 3-5 ms at 1 kHz and 1 ms at 4 kHz). Such peaks were still apparent, but smaller in the no-noise condition and were almost absent at the higher noise level. For the 0.25-kHz signal frequency, peaks were not observed consistently at any level, although two subjects showed small peaks for durations around 10 ms. An explanation is offered for the results in terms of the level and frequency dependence of basilar-membrane input-output functions.

Auditory Perception↗

Inter-relationship between different psychoacoustic measures assumed to be related to the cochlear active mechanism.

The active mechanism in the cochlea is thought to depend on the integrity of the outer hair cells (OHCs). Cochlear hearing loss is usually associated with damage to both inner hair cells (IHCs) and OHCs, with the latter resulting in a reduction in or complete loss of the function of the active mechanism. It is believed that the active mechanism contributes to the sharpness of tuning on the basilar membrane (BM) and is also responsible for compressive input-output functions on the BM. Hence, one would expect a close relationship between measures of sharpness of tuning and measures of compression. This idea was tested by comparing three different measures of the status of the active mechanism, at center frequencies of 2, 4, and 6 kHz, using subjects with normal hearing, with unilateral or highly asymmetric cochlear hearing loss, and with bilateral loss. The first measure, HLOHC, was an indirect measure of the amount of the hearing loss attributable to OHC damage; this was based on loudness matches between the two ears of subjects with unilateral hearing loss and was derived using a loudness model. The second measure was the equivalent rectangular bandwidth (ERB) of the auditory filter, which was estimated using the notched-noise method. The third measure was based on the slopes of growth-of-masking functions obtained in forward masking. The ratio of slopes for a masker centered well below the signal frequency and a masker centered at the signal frequency gives a measure of BM compression at the place corresponding to the signal frequency; a ratio close to 1 indicates little or no compression, while ratios less than 1 indicate that compression is occurring at the signal place. Generally, the results showed the expected pattern. The ERB tended to increase with increasing HLOHC. The ratio of the forward-masking slopes increased from about 0.3 to about 1 as HLOHC increased from 0 to 55 dB. The ratio of the slopes was highly correlated with the ERB (r = 0.92), indicating that the sharpness of the auditory filter decreases as the compression on the BM decreases.

Adult↗