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PubMed1992

Effect of multiple speechlike maskers on binaural speech recognition in normal and impaired hearing.

Speech-reception thresholds (SRT) were measured for 17 normal-hearing and 17 hearing-impaired listeners in conditions simulating free-field situations with between one and six interfering talkers. The stimuli, speech and noise with identical long-term average spectra, were recorded with a KEMAR manikin in an anechoic room and presented to the subjects through headphones. The noise was modulated using the envelope fluctuations of the speech. Several conditions were simulated with the speaker always in front of the listener and the maskers either also in front, or positioned in a symmetrical or asymmetrical configuration around the listener. Results show that the hearing impaired have significantly poorer performance than the normal hearing in all conditions. The mean SRT differences between the groups range from 4.2-10 dB. It appears that the modulations in the masker act as an important cue for the normal-hearing listeners, who experience up to 5-dB release from masking, while being hardly beneficial for the hearing impaired listeners. The gain occurring when maskers are moved from the frontal position to positions around the listener varies from 1.5 to 8 dB for the normal hearing, and from 1 to 6.5 dB for the hearing impaired. It depends strongly on the number of maskers and their positions, but less on hearing impairment. The difference between the SRTs for binaural and best-ear listening (the "cocktail party effect") is approximately 3 dB in all conditions for both the normal-hearing and the hearing-impaired listeners.

Adult↗
PubMed1992

Psychometric functions for level discrimination and the effects of signal duration in the goldfish (Carassius auratus): psychophysics and neurophysiology.

Classical conditioning of respiration was used to obtain psychometric functions for pulsed tone level discrimination in the goldfish (Carassius auratus). Conditioned respiratory suppression is a graded response that has some properties of a confidence rating measure. These properties were used to obtain receiver operating characteristics (ROC) and psychometric functions using a blocked method of constant stimuli. Empirical ROCs and neurometric functions were also obtained for single auditory-nerve fibers using spike count as the decision variable in order to evaluate a simple rate code for level discrimination. Psychometric and neurometric functions for level discrimination are similar in showing the same general form (summarized by Weibull functions) that is independent of signal duration. The lower slope of neurometric functions compared with behavioral functions for level discrimination is in accord with similar data on sound detection and vision in nonhuman mammals. Both neural and psychophysical level discrimination thresholds decline with increasing duration (20 to 320 ms), with similar slopes except at short signal durations (20 to 50 ms). At these durations, the animal's use of a channel-selection strategy and neural information following stimulus offset could reduce the difference between neural and psychophysical thresholds. The slopes of the neural and psychophysical duration functions are similar to those for human observers, but the majority of auditory-nerve fibers sampled have lower level discrimination thresholds than the behaving animal. Since human observers perform better than the majority of neurons in level discrimination, well-trained human listeners may be able to select channels with superior information, or to combine information across channels in ways that the goldfish and other animals do not. In general, one is encouraged to believe that neural mechanisms need not be more complex or sensitive than those considered here to account for pure-tone level discrimination in fishes, humans, and other vertebrates.

Animals↗
PubMed1992

Effects of roving level variation on monaural detection with a contralateral cue.

Monaural detection with a contralateral cue (MDCC) was measured with and without a 20-dB overall roving level to determine the contribution of loudness to performance on this task. Psychometric functions were obtained for three normal-hearing subjects as a function of the signal-to-noise ratio for pure-tone and 1/3-oct noiseband signals at 500 and 4000 Hz with a wideband noise masker. At 4000 Hz, the roving level degrades performance for the narrow-band noise signal by about 5.3 dB. In addition, the presence of the contralateral cue degrades performance for both the pure-tone and narrow-band noise signals at 4000 Hz by 3 to 6 dB. At 500 Hz, however, performance is not affected by the roving level, and is improved by 3 to 6 dB by the contralateral cue. These results indicate that loudness is being used as a cue only for detection of the 4000-Hz narrow-band noise.

Acoustics↗
PubMed1992

The effects of notched noise on intensity discrimination under forward masking.

Zeng et al. [Hear. Res. 55, 223-230 (1991)] reported that at moderate levels there is an increase in the intensity jnd for 25-ms sinusoidal pedestals presented 100 ms after an intense narrow-band noise. They suggested that this effect is related to the finding that low spontaneous rate (SR) auditory-nerve neurons take a considerable time to recover from adaptation [E. M. Relkin and J. R. Doucet, Hear. Res. 55, 215-222 (1991)]: 100 ms after the noise, the low-SR neurons still have elevated thresholds. Therefore, the intensity of a pedestal falling between the saturation level of the high-SR neurons and the elevated threshold of the low-SR neurons will be poorly represented in neutral firing rates, and the jnd will be high. A problem with this interpretation is that subjects may listen "off frequency." Theoretically, it should always be possible to choose a frequency channel for which the pedestal level is within the dynamic range of the high-SR neurons. In the present study, the experiment of Zeng et al. was replicated but with the pedestal presented in the temporal center of a notched noise to prevent off-frequency listening. Surprisingly, the notched noise substantially decreased the jnd at mid levels, removing or severely reducing the mid-level jnd elevation. This was true for pedestal frequencies of 1 and 6 kHz. It was also found that even if the notched noise was terminated before pedestal onset the jnd elevation was reduced. This suggests that the effect of the notched noise is not due to suppression.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1992

Discrimination of narrow-band spectra. I: Spectral weights and pitch cues.

The ability to detect changes in the spectral shape of narrow-band tonal complexes (spectral profiles) is examined. The standard consists of three tones of equal intensity; thresholds for detecting an increment in the level of the central, 1000-Hz tone are estimated. A roving-level procedure is used in order to impose a statistical limit on thresholds that can be obtained by basing discriminations on absolute intensity. Estimated thresholds are consistently below this limit, thus indicating the use of other cues. Generally, thresholds are constant for bandwidths ranging from less than a critical band to greater than several octaves. Spectral weight estimates, however, are highly dependent on bandwidth, providing evidence that the discrimination of narrow-band spectra involves different auditory processes than those used to discriminate wideband spectra. Additional data show that pitch cues are important within a restricted range of intermediate bandwidth, but not for wideband or very narrow-band spectra. A version of the EWAIF model involving off-frequency listening is proposed to account for the results.

Adolescent↗
PubMed1992

Asymmetrical discrimination of narrow-band stimuli.

A three-interval, forced-choice procedure that obtained complete psychometric functions was used to study frequency discrimination for 13-item continua of impulse-generated, narrow-band, buzz-like, steady-state sounds. For all subjects and durations, discrimination relative to the highest center frequency (1060 Hz) stimuli was better than discrimination relative to the lowest center frequency (940 Hz). This result is not in consonance with traditional reports of pure tone frequency discrimination and is not readily explained. However, additional experiments with similar stimuli replicated these findings.

Adult↗
PubMed1992

Directional dependence of auditory sensitivity and frequency selectivity in the leopard frog.

Direction-dependent changes in frequency selectivity were documented in three populations of neurons in the auditory periphery of the leopard frog: low-, mid-, and high-frequency sensitive fibers. These changes were most pronounced in the mid-frequency (720-1199 Hz) sensitive fibers which exhibited positive shifts in characteristic frequencies (CFs) and concomitant narrowed bandwidths from posterior speaker presentations. Maximum sensitivities were observed for ipsilateral speaker presentations in these fibers. Low-frequency (63-500 Hz) sensitive fibers exhibited mean threshold shifts at their CFs of up to -7 dB with posterior speaker presentations. Low- and high-frequency sensitive fibers whose CFs closely correspond to the peaks of spectral energy of the species' mating call were the most sensitive (exhibited lowest thresholds) but showed little directional-dependent frequency selectivity. Directional-dependent variation in frequency selectivity and sensitivity in low- and mid-frequency sensitive fibers was attributed to pressure and phase differences impinging on the inner surface of the eardrum.

Animals↗
PubMed1992

Auditory filter bandwidths in binaural and monaural listening conditions.

The shape and the effective bandwidth of the auditory filter at 500 Hz was examined for binaural and monaural tone-in-noise detection experiments in four normal listeners. In the binaural condition, a broadband noise with an interaural phase difference of 0 below and an interaural phase difference of pi above a certain "edge frequency" was employed to mask a 500-Hz probe tone with an interaural phase pi (denoted as No pi S pi). The threshold of the probe tone as a function of the edge frequency in this configuration and in a configuration with an inverted interaural phase of the masker (denoted as N pi oS pi) was fitted by assuming different filter shapes and optimizing their respective parameters. In an analogous monaural experiment, the spectral power density of the masker was 15 dB lower below the "edge frequency" or 15 dB lower above this frequency, respectively. Several filter characteristics with two free parameters describe the data almost equally well. Their equivalent rectangular bandwidths (ERB) show considerably more variations between filter shapes than the 10-dB bandwidth and the 90% bandwidth values (i.e., the bandwidths encompassing 90% of the integrated area above and below the center frequency). This indicates that either of these two bandwidth parameters is more appropriate for comparing auditory filter bandwidths than the ERB. For the rounded exponential filter, the 90% bandwidth averages to 147 Hz in the binaural and to 125 Hz in the monaural condition. These values are up to 12% higher if off-frequency detection is accounted for. Our general finding of auditory filter bandwidths in the binaural conditions exceeding the monaural bandwidths by approximately 20% may be caused by two factors: First, off-frequency detection may be performed in monaural, but not in binaural detections tasks and second, the random interaural mismatch in binaural noise reduction processes fluctuates slowly and thus modulates and spectrally smears the output signal of the binaural noise reduction process.

Adult↗
PubMed1993

Intensity just-noticeable differences at equal-loudness levels in normal and pathological ears.

The relationship between loudness level and intensity discrimination was investigated in the frequency range 0.5-6.5 kHz by comparing the intensity just-noticeable differences (jnd's) at a number of equal-loudness levels in the better and poorer ears of eight individuals with essentially unilateral hearing loss of cochlear origin. Such hearing loss usually produces loudness recruitment, altering the relationships among the loudness, sound-pressure level (SPL), and sensation-level (SL) variables, so that their effects can be separated. In these experiments, the jnd's were correlated with loudness level, not SPL or SL. Although, in some listeners, there were significant differences between jnd's in the two ears at some binaurally equal-loudness levels, they were not systematic over the group of listeners. Statistically, there was no significant difference between equal-loudness jnd's in the two ears, whereas the corresponding SLs and SPLs were significantly different. The rate of loudness growth had no effect on the jnd's. As expected from the near-miss to Weber's law, the mean jnd's decreased with sound intensity. The corresponding decrease in the mean Weber fraction, delta I/I, was accompanied by a decrement in its intrasubject standard deviation. The latter was correlated with the mean, independent of its relationship to SPL or SL.

Acoustic Stimulation↗
PubMed1993

Temporary threshold and loudness shifts: frequency patterns and correlations.

Two experiments studied the frequency pattern of TLS (temporary loudness shift) as a function of the level and frequency of the fatiguing sound. In experiment 1, the fatiguing tones were intermittent 375-, 1500-, or 3000-Hz tones (10 s on/10 s off) at 75, 80, 85, 90, or 95 dB SPL. The TLS patterns were established for a continuous, 60-phon test tone at different frequencies presented simultaneously with the intermittent fatiguing tone. In experiment 2, a 1000-Hz exposure tone with an intermittency of 10 s on/20 s off was used with a continuous 60-dB test tone at different frequencies. In both experiments, the total exposure duration was 60 s; TLS was measured 5 s after the exposure ended. For the lowest two exposure levels, the TLS pattern had one peak centered on the exposure frequency. As the exposure level increased, a two-peak pattern became evident, with the second peak at higher test frequencies. This finding could be interpreted as psychoacoustical evidence for the double (passive and active) mode of displacement of the basilar membrane. In experiment 2, a TTS (temporary threshold shift) measurement after exposure to a 45-min, 1000-Hz tone at 90 dB was added to the TLS sessions. The correlations between maximum TTS after a 45-min exposure and the TLS obtained after a 60-s exposure were calculated for each of the exposure levels and test frequencies used in TLS measurements. The correlation reached as high as 0.9 for TLSs measured at 1120 Hz after a 90-dB exposure; it was smaller but significant for TLSs at the exposure frequency. Despite these correlations, differences in the overall patterns of TTS and TLS suggest that they stem from two different mechanisms.

Acoustic Stimulation↗
PubMed1993

Where the action is: Weber fractions as a function of sound pressure at low frequencies.

Weber fractions for sound intensity were measured for 70-, 100-, 200-, 1000-, and 10,000-Hz tone pulses at sound-pressure levels (SPLs) ranging from just above individual listeners' absolute thresholds to near their highest tolerable SPLs, using a two-alternative forced-choice adaptive staircase technique governed by a 1-up, 3-down rule. Results for four listeners with normal hearing and varying experience, despite individual differences in absolute values, showed Weber fractions that declined as sound pressure increased above threshold and asymptoted at intermediate SPLs. A power function with a negative exponent describes the data of the individual listeners better than a logarithmic function does. The absolute value of the exponent of the power function, which measures the curvature of the function, was largest at 70 Hz and declined with increasing frequency, similar to how exponents of power functions relating loudness judgments or simple reaction time to stimulus intensity differ with sound frequency.

Acoustic Stimulation↗
PubMed1993

Simulation of the effects of loudness recruitment and threshold elevation on the intelligibility of speech in quiet and in a background of speech.

These experiments simulated the threshold elevation and loudness recruitment associated with three different types of cochlear hearing loss: Moderate flat (condition R2), severe flat (condition R3), and moderate-to-severe sloping (condition RX). This was done to allow an examination of the effects of these factors on the intelligibility of speech, in isolation from other factors that are normally associated with cochlear hearing loss, such as reduced frequency selectivity. The simulation was performed by splitting the input signal into 13 frequency bands, and processing the envelope in each band so as to create loudness sensations in a normal ear that would resemble those produced in an impaired ear with recruitment. The bands were then recombined. All tests were performed using subjects with normal hearing. For speech in quiet, simulation of hearing loss produced a reduction in the ability to understand low-level speech. However, speech at sufficiently high levels was highly intelligible in all conditions. Linear amplification according to the National Acoustic Laboratory (NAL) prescription gave high intelligibility for speech at normal conversational levels. For speech presented at a fixed input level of 65 dB SPL, against a background of a single competing talker, simulation of hearing loss produced substantial decrements in performance. The speech-to-background ratios in conditions R2 and RX had to be 11-13 dB higher than in the control condition (unprocessed stimuli) to achieve similar levels of performance. Linear amplification according to the NAL prescription improved performance markedly for the conditions simulating flat losses, but was less effective for the condition simulating a sloping loss. This indicates that threshold elevation combined with recruitment produces a loss of intelligibility for speech in the presence of a single competing talker that is only partly compensated by linear amplification of the type typically used in hearing aids.

Acoustic Stimulation↗
PubMed1993

Functional changes in the ventral cochlear nucleus following acute acoustic overstimulation.

The effects of acute acoustic overstimulation on the discharge patterns of neurons in the ventral cochlear nucleus (VCN) were evaluated in anesthetized chinchillas. Response measures were obtained from the same neuron before and after presenting a 3- to 5-min intense tone (90-105 dB SPL) located one-half oct above the unit's characteristic frequency (CF). If a unit had an inhibitory response area at frequencies above CF and if the traumatizing tone reduced the magnitude of the inhibitory response, then the neuron's discharge rate to suprathreshold tones at CF increased ("enhancement") by as much as 25%. However, if a unit lacked an inhibitory response area at frequencies above CF, then the traumatizing tone typically caused either no change or a decrease in the unit's discharge rate at CF. The traumatizing tone did not alter the shape of the post-stimulus time histograms. Moreover, the width of the excitatory response area was not altered by the exposure even when traumatizing stimulus reduced the magnitude of the inhibitory response above CF. The enhanced firing rate at CF following the exposure could conceivably contribute to the enhanced evoked-potential amplitudes observed in the auditory brain stem following acoustic trauma.

Acoustic Stimulation↗
PubMed1994

Excitation patterns in the starling cochlea: a population study of primary auditory afferents.

The excitatory effect of different test stimuli was quantified in a large sample of primary auditory units of the starling. In order to construct an excitation pattern, the level of excitation in many single units in response to a specific test stimulus was plotted as a function of their characteristic frequency (CF). The effects of stimulus frequency and stimulus sound-pressure level on the shapes of the excitation patterns were characterized by measuring excitation patterns in response to 33 different test stimuli which covered a range of frequencies (0.125 to 2.0 kHz) and sound-pressure levels (20 to 90 dB SPL). In contrast to the mammalian situation, excitation patterns in the starling showed a systematic asymmetry with the high-frequency side being, on average, twice as steep as the low-frequency side. In addition, the sound-pressure level had no systematic effect on the symmetry or on the high- and low-frequency slopes of the flanks of the excitation patterns. Thus, the nonlinear growth of excitation with increasing sound-pressure level that is typical for the high-frequency flank of mammalian excitation patterns, was not found in the starling. The differences in mammalian and avian excitation patterns are probably related to systematic differences in tuning characteristics of the respective hearing organs.

Animals↗
PubMed1994

Discrimination of random, time-varying spectra with statistical constraints.

In the present study, a sample-discrimination procedure is used to examine how various statistical constraints on random, time-varying spectra might aid listeners in discriminating among these signals. Time-varying spectra were constructed by adding five sequences of tones, five tones in each sequence, centered at the octave frequencies from 250 to 4000 Hz. The levels, frequencies, and durations of the tones varied randomly from one presentation to the next. The signal to be detected was an increment in the level of tones comprising the sequence centered at 1000 Hz (the target sequence). Three main conditions were examined in which the parameter values of tones varied independently of one another (equal-variance condition), covaried across tone sequences (cross-channel covariance condition), or covaried among themselves for each tone (cross-parameter covariance condition). For the latter two conditions, two special cases were examined in which the target sequence varied independently of nontarget sequences or varied according to the same statistical rules. For five of six listeners, comparisons of performance to that of an ideal, within-channel observer gave clear evidence of an ability to take advantage of cross-channel statistical constraints, but only when the target sequence varied independently of its context. Results offer no evidence for listeners' ability to take advantage of cross-parameter constraints. Trial-by-trial analyses in the equal-variance condition identify factors other than the appropriate weighting of information as primarily responsible for suboptimal performance, though individual differences complicate this interpretation. A failure of simple detection-theoretic models to account for these results is discussed in terms of possible perceptual rules governing sound source identification of real-world objects.

Adult↗
PubMed1994

Level-dependent critical bandwidth for phase discrimination.

Monaural phase discrimination was evaluated at 1000 Hz in six normal-hearing listeners as a function of the frequency difference between components in three-tone complexes at 40, 60, 80, and 100 dB SPL. The phase of the center component of 100% sinusoidally amplitude-modulated (SAM) waveforms was shifted by 90 degrees to produce quasi-frequency-modulated (QFM) waveforms that had identical long-term power spectra to the SAM waveforms but with different amplitude envelopes and temporal fine structure. At low modulation frequencies, where spectral components were close together and presumably all well within a single auditory filter, normal-hearing listeners could easily discriminate QFM from SAM waveforms. As modulation frequency increased, a point was reached where listeners could no longer distinguish QFM from SAM waveforms, referred to here as the critical bandwidth for phase discrimination (CBphs). Discrimination performance (d') was measured as a function of modulation frequency to yield a psychometric function for phase discrimination. From the psychometric function, CBphs was defined as the modulation frequency corresponding to d' = 1.0. At a carrier frequency of 1000 Hz, CBphs increased with level between 40 and 80 dB SPL according to the relation: CBphs = 34.I(0.136). Above 80 dB SPL, very little change in CBphs with level was seen. The increase with level of the geometric mean CBphs was predicted from level-dependent auditory filter slopes inferred from forward-masked tuning curves, as was the tendency to reach an asymptote above 80 dB SPL. Comparisons with previous work indicate that CBphs values from the best performing subjects were well within the audibility region for cubic difference tones. It is proposed that internally generated cubic difference tones interact with externally generated acoustic components, both limited by a level-dependent auditory filter, to produce an internal excitation envelope that is the basis for discriminating between SAM and QFM waveforms. It is also suggested that individual differences at low levels may be due to internal phase ambiguities.

Attention↗
PubMed1994

The middle ear muscle of frogs does not modulate tympanic responses to sound.

The effect of the opercularis (= middle ear) muscle on the acoustic responsiveness of the tympanic middle ear of anuran amphibians was studied using laser vibrometric measurements of tympanic responses to sound. Removal of the muscle or direct stimulation of denervated muscles had no measurable effects on tympanic responses to sound in either American bullfrogs (Rana catesbeiana) or green treefrogs (Hyla cinerea) at any frequency or at any sound-pressure level studied. These results suggest that, contrary to proposed hypotheses, the opercularis muscle of the anuran middle ear is not capable of modulating the responsiveness of the tympanic middle ear. Instead, the opercularis system most likely functions as an independent system involved in acoustic reception.

Acoustic Stimulation↗
PubMed1994

Gerbil brain-stem auditory-evoked responses to maximum length sequences.

This study evaluated the feasibility of obtaining brain-stem auditory-evoked responses (BAERs) to trains of clicks with average rates of up to 500 clicks per second in the gerbil, in order to evaluate BAER behavior at rates higher than those possible in conventional averaging, and to evaluate whether these higher rates allow obtaining BAERs more efficiently. Gerbils were anesthetized with Nembutal, and normothermia was maintained with a homeothermic blanket system. Pseudorandom pulse trains, called maximum length sequences (MLSs), were generated by an Ariel DSP-16 board housed in an IBM-AT. Electrical activity was recorded with Grass needle electrodes placed subdermally. This activity was amplified and filtered by a Nicolet Compact Four, and digitized by the A/D of the Ariel DSP-16. Clicks were presented at levels of 50, 60, 70, 80, and 90 dB pSPL. Conventional BAERs were obtained at a rate of 30 Hz. MLS BAERs were obtained by presenting MLS pulse trains which were comprised of 64 pulses. Following collection of the response to MLS pulse trains, the MLS BAER was obtained by cross correlating the response with a recovery sequence. The minimum time between pulses is called the minimum pulse interval (MPI). MLS BAERs were obtained for MPIs of 6, 4, 2, and 1 ms. BAERs were obtained in ten young adult gerbils for all rate by click-level conditions. BAERs were observed in all animals for all click levels and rates. Generally, with increasing click level there were decreases in peak latencies and increases in peak amplitudes. With increasing rate (decreasing MPI), there were increases in peak latencies, increases in the i-iv interval, and decreases in peak amplitudes. Computations suggested the the most efficient rate (i.e., the rate producing a constant signal-to-noise ratio response in the least amount of time) is not necessarily the fastest rate, but depends on the BAER peak and click level.

Acoustic Stimulation↗