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Discrimination of modulation depth of sinusoidal amplitude modulation (SAM) noise.

The detection of sinusoidal amplitude modulation (SAM) provides a lower bound on the degree to which temporal information in the envelope of complex waveforms is encoded by the auditory system. The extent to which changes in the amount of modulation are discriminable provides additional information on the ability of the auditory system to utilize envelope fluctuations. Results from an experiment on the discrimination of modulation depth of broadband noise are presented. Discrimination thresholds, expressed as differences in modulation power, increase monotonically with the modulation depth of the standard, but do not obey Weber's law. The effects of carrier level and of modulation frequency are consistent with those observed in modulation detection: Changes in carrier level have little effect on modulation discrimination; changes in modulation frequency also have little effect except for standards near the modulation detection threshold. The discrimination of modulation depth is consistent with the leaky-integrator model of modulation detection for standards below--10 dB (20 log ms); for standards greater than--10 dB, the leaky integrator predicts better performance than that observed behaviorally.

Attention↗

Auditory temporal integration in the normal-hearing and hearing-impaired cat.

Temporal integration functions obtained from human subjects with sensorineural hearing loss have shallower slopes than the functions obtained from normal-hearing subjects. The present investigation was designed to explore this relation in animals in order to compare normal-hearing cats and humans. Auditory temporal integration functions were measured for five cats before and after they were exposed to a 2-kHz tone at 110 dB SPL for 48 h. To measure the temporal integration functions, ten stimuli were used that had overall durations from 8.32 to 275 ms and that were configured either as single or multiple tone bursts of 6.25 kHz. Twelve thresholds for each stimulus were obtained from each animal before and after the sound exposure. Pre- and postexposure audiograms were also obtained and the mean permanent threshold shift at 6.25 kHz was 32.5 dB. Exponential and power function models were used to describe the data. The exponential model (with grand-mean data) yielded a pre-exposure time constant (tau) of 188 ms [mean absolute residual (MAR) of 1.5 dB] and a postexposure tau of 21 ms (MAR of 1.4 dB). For the power function model with grand-mean data, the pre-exposure slope was 6.6 dB per decade of duration (MAR of 1.4 dB) and a postexposure slope of 3.8 dB per decade of duration (MAR of 0.7 dB). The results indicated that the slope of the temporal integration function was less steep after sensorineural hearing loss of cochlear origin, and that the power function model was more effective in describing temporal integration data for the range of stimulus durations employed.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Temporal integration in amplitude modulation detection.

Thresholds for detecting sinusoidal amplitude modulation (AM) of a wideband noise carrier were measured as a function of the duration of the modulating signal. The carrier was either; (a) gated with a duration that exceeded the duration of modulation by the combined stimulus rise and fall times; (b) presented with a fixed duration that included a 500-ms carrier fringe preceding the onset of modulation; or (c) on continuously. In condition (a), the gated-carrier temporal modulation transfer functions (TMTFs) exhibited a bandpass characteristic. For AM frequencies above the individual subject's TMTF high-pass segment, the mean slope of the integration functions was - 7.46 dB per log unit duration. For the fringe and continuous-carrier conditions [(b) and (c)], the mean slopes of the integration functions were, respectively, - 9.30 and - 9.36 dB per log unit duration. Simulations based on integration of the output of an envelope detector approximate the results from the gated-carrier conditions. The more rapid rates of integration obtained in the fringe and continuous-carrier conditions may be due to "overintegration" where, at brief modulation durations, portions of the unmodulated carrier envelope are included in the integration of modulating signal energy.

Adult↗

Observer efficiency and weights in a multiple observation task.

A sequence of seven tones, sampled from one of two distributions differing in mean frequency, is presented to observers who try to report which distribution was sampled. Estimates are obtained of the weight or importance given to each tone as a function of its temporal position. In five experiments, the reliability of the information is varied by changing the variance of the distributions; tones with high reliability are sampled from distributions with relatively small variance, whereas tones with low reliability are sampled from distributions with relatively large variance. Results show that the observations are weighted more efficiently when the tones have equal rather than unequal reliability, and when the most reliable tones have the greater intensity. Additional results show that the most intense tones often receive the greatest weight, even when those tones have the least reliability.

Adult↗

Amplitude and frequency fluctuations of spontaneous otoacoustic emissions.

Amplitude and frequency fluctuations of spontaneous otoacoustic emissions have been studied. Spontaneous otoacoustic emissions were recorded from eight human ears and two frog ears (Rana esculenta). Record length typically was 80 s. For a recorded emission signal, the amplitude signal A(t) (average A0) and time intervals T(ti) between successive positive-going zero crossings (i counts zero crossings) were determined. Emission amplitude and period both showed small fluctuations: delta Arms/A0 ranged from 0.7 X 10(-2) to 6.3 X 10(-2) for human emissions and was 24 X 10(-2) for both frog emissions; delta Trms ranged from 1.4 to 6.9 X 10(-7) s for human emission and was 50.0 and 55.0 X 10(-7) s for the two frog emissions. There was a positive correlation between delta Arms/A0 and delta Trms as determined for different emissions (R = 0.9). Spectra of A(t) and T(ti) revealed that amplitude and period were slowly fluctuating functions: cutoff frequency delta f delta A of the amplitude spectrum ranged from 3 to 18 Hz; delta f delta T ranged from 7 to 32 Hz. Results have been compared to amplitude and frequency fluctuations of a second-order oscillator, that interacts with a noise source. It has been concluded that an oscillator with linear stiffness (for example a Van der Pol oscillator) driven by white Gaussian noise, cannot account for all experimental results. Other possible oscillators (e.g., nonlinear stiffness) and noise sources (e.g., narrow-band noise), that may account for the observed phenomena, are discussed.

Animals↗

Effects of fluctuating noise and interfering speech on the speech-reception threshold for impaired and normal hearing.

The speech-reception threshold (SRT) for sentences presented in a fluctuating interfering background sound of 80 dBA SPL is measured for 20 normal-hearing listeners and 20 listeners with sensorineural hearing impairment. The interfering sounds range from steady-state noise, via modulated noise, to a single competing voice. Two voices are used, one male and one female, and the spectrum of the masker is shaped according to these voices. For both voices, the SRT is measured as well in noise spectrally shaped according to the target voice as shaped according to the other voice. The results show that, for normal-hearing listeners, the SRT for sentences in modulated noise is 4-6 dB lower than for steady-state noise; for sentences masked by a competing voice, this difference is 6-8 dB. For listeners with moderate sensorineural hearing loss, elevated thresholds are obtained without an appreciable effect of masker fluctuations. The implications of these results for estimating a hearing handicap in everyday conditions are discussed. By using the articulation index (AI), it is shown that hearing-impaired individuals perform poorer than suggested by the loss of audibility for some parts of the speech signal. Finally, three mechanisms are discussed that contribute to the absence of unmasking by masker fluctuations in hearing-impaired listeners. The low sensation level at which the impaired listeners receive the masker seems a major determinant. The second and third factors are: reduced temporal resolution and a reduction in comodulation masking release, respectively.

Adolescent↗

A parametric study of cochlear input impedance.

In this paper various aspects of the cat cochlear input impedance Zc (omega) are implemented using a transmission line model having perilymph viscosity and a varying cross-sectional scalae area. These model results are then compared to the experimental results of Lynch et al. [J. Acoust. Soc. Am. 72, 108-130 (1982)]. From the model, the following observations are made about the cochlear input impedance: (a) Scalae area variations significantly alter the model Zc (omega); (b) the use of anatomically measured area improves the fits to the experimental data; (c) improved agreement between model and experimental phase is obtained when perilymph viscosity and tapering are included in the cochlear model for frequencies below approximately 150 Hz; (d) when model scalae tapering and perilymph viscosity are chosen to match physiological conditions, the effect of the helicotrema impedance on Zc (omega) is insignificant; and (e) the cochlear map, which is defined as the position of the basilar membrane peak displacement as a function of stimulus frequency, can have an important effect on Zc (omega) for frequencies below 500 Hz. A nonphysiological cochlear map can give rise to cochlear standing waves, which result in oscillations in Zc (omega). Scalae tapering and perilymph viscosity contribute significantly to the damping of these standing waves. These observations should dispel the previous notion that Zc (omega) is determined solely by parameters of the cochlea close to the stapes, and the notion that Zc (omega) is dominated by the helicotrema at low frequencies.

Acoustic Impedance Tests↗

Manifestations of intense noise stimulation on spontaneous otoacoustic emission and threshold microstructure: experiment and model.

Comparison between changes that occur simultaneously on spontaneous otoacoustic emissions (SOAEs) and on other cochlear origin phenomena can contribute to the understanding of cochlear micromechanical activity. The temporary changes that arise after short noise exposure are investigated in the following paper. The effects of noise exposure on the threshold microstructure near an SOAE and on the amplitude and frequency of the SOAE were measured. These experimental results indicate the following: (1) exposure to wideband noise for a short time causes a temporary reduction in the SOAE frequency and amplitude, and alters reversibly the threshold microstructure in the vicinity of the SOAE. The difference between the minimum and maximum in the threshold microstructure is reduced, and the frequency that yields the minimum threshold decreases; (2) the threshold at the SOAE frequency is most sensitive to noise exposure; (3) intense stimulation causes a relatively small increase, or even a decrease, in threshold at frequencies near the SOAE. The experimental results are interpreted in terms of a nonlinear transmission line model which includes nonlinear amplifiers. The effect of the noise exposure is modeled by reduction in the cochlear partition amplification term. Most of the experimental results are predicted by this model.

Auditory Fatigue↗

Intensity and frequency resolution: masking of absolute identification and fixed and roving discrimination.

Auditory intensity and frequency resolution were studied in three paradigms under masking conditions. Absolute identifications of single stimuli (one-interval paradigm) and 2IFC judgments of fixed- and roving-level pairs of stimuli (two-interval paradigm) were obtained from the same experienced observers. Judgments were made under optimal (no mask) conditions, in the presence of a broadband noise mask (simultaneous mask), and when the stimulus(i) to be judged were either preceded (forward mask) or followed (backward mask) by a broadband noise mask. Substantial masking of intensity resolution was found in all mask conditions. Only a simultaneous mask affected frequency resolution. In the no mask condition, performance was best for fixed-level (or frequency) 2IFC discrimination, followed by roving-level (frequency) 2IFC, and finally absolute identification. These differences were maintained under masking for frequency resolution, but not for intensity resolution. The results are discussed in terms of the Braida and Durlach (1988) model of intensity resolution. A similar model is suggested for frequency resolution with differences suggested by the differences in neural coding of sound intensity and frequency.

Auditory Perception↗

Speech pattern hearing aids for the profoundly hearing impaired: speech perception and auditory abilities.

A family of prototype speech pattern hearing aids for the profoundly hearing impaired has been compared to amplification. These aids are designed to extract acoustic speech patterns that convey essential phonetic contrasts, and to match this information to residual receptive abilities. In the first study, the presentation of voice fundamental frequency information from a wearable SiVo (sinusoidal voice) aid was compared to amplification in 11 profoundly deafened adults. Intonation reception was often better, and never worse, with fundamental frequency information. Four subjects scored more highly in audio-visual consonant identification with fundamental frequency information, five performed better with amplified speech, and two performed similarly under these two conditions. Five of the 11 subjects continued use of the SiVo aid after the tests were complete. A second study examined a laboratory prototype compound speech pattern aid, which encoded voice fundamental frequency, amplitude envelope, and the presence of voiceless excitation. In five profoundly deafened adults, performance was better in consonant identification when additional speech patterns were present than with fundamental frequency alone; the main advantage was derived from amplitude information. In both consonant identification and connected discourse tracking, performance with appropriately matched compound speech pattern signals was better than with amplified speech in three subjects, and similar to performance with amplified speech in the other two. In nine subjects, frequency discrimination, gap detection, and frequency selectivity were measured, and were compared to speech receptive abilities with both amplification and fundamental frequency presentation. The subjects who showed the greatest advantage from fundamental frequency presentation showed the greatest average hearing losses, and the least degree of frequency selectivity. Compound speech pattern aids appear to be more effective for some profoundly hearing-impaired listeners than conventional amplifying aids, and may be a valuable alternative to cochlear implants.

Adult↗

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.

Acoustics↗

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↗

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↗

Single neurons in the frog inferior colliculus exhibit direction-dependent frequency selectivity to isointensity tone bursts.

The effects of sound direction on frequency selectivity of inferior colliculus (IC) neurons were investigated by measuring the neuron's isointensity frequency responses (FRs) to tone bursts emanating from a free-field loudspeaker at several sound levels. The loudspeaker was rotated across the frontal field at 0 degrees elevation through 180 degrees of azimuth (from contralateral 90 degrees or C90 degrees to ipsilateral 90 degrees or I90 degrees). At each frequency, to assess the magnitude of response change with sound direction, the mean spike count obtained at an azimuth was compared to that at C90 degrees. The FR of most IC neurons (75/83 or 90%) was direction dependent. For most of these neurons, bandwidths of FRs were narrower when sounds originated from ipsilateral azimuths. Remarkably, with a change in sound azimuth, some segments of these FRs showed very distinct changes in shape, while other portions of the same FRs remained essentially unchanged. These narrow-band changes associated with restricted portions of the FR, were also exhibited by neurons with direction-dependent frequency-threshold characteristics (Gooler et al., 1993). Additionally, the most frequent direction-dependent change in the FRs occurred in a narrow frequency band around the units' best excitatory frequency.

Acoustic Stimulation↗

Vibrotactile temporal masking: effects of multiple maskers.

Previous investigations of temporal masking effects in vibrotactile detection tasks have generally produced results suggesting considerable similarities in stimulus processing between the tactile system and the auditory system. Auditory presentation of combinations of maskers (e.g., two forward maskers) has yielded masking effects in excess of the level of masking predicted by a simple intensity sum of each masker's individual effect. This "additional masking" has led to predictions of compressive nonlinearities in auditory stimulus processing. In the present study, two experiments were conducted to investigate further temporal masking phenomena for the tactile system. In the first experiment vibrotactile temporal masking functions for single forward and backward maskers were generated to examine trade-offs among values of masker duration, masking intensity, and interstimulus interval to maintain constant detectability of a target. Results suggested that stimuli in very close temporal proximity to the target might follow somewhat different trading equations from those farther removed. Overall, results were consistent with previous findings of temporal integration in the tactile system, and support the notion of an energy integrating mechanism. In the second experiment, pairs of maskers were presented to determine whether additional masking effects occurred in vibrotactile detection. In contrast to findings for auditory presentation, in which all masker configurations generated additional masking, the tactile results showed substantial amounts of additional masking only for pairs of backward maskers. Several possible explanations for this results are evaluated, and results are discussed in terms of similarities and dissimilarities in auditory and tactile temporal processing.

Adult↗

A perceptual study of source coding of Fourier phase and amplitude of the linear predictive coding residual of vowel sounds.

A practical question in a Fourier transform coding of speech signals is to what accuracy their amplitude and phase spectra have to be represented without perceptible distortions. In this paper a concern is with the audibility of quantization noise signals which are produced by quantizing the amplitude and phase spectra of vowel sounds. Experiments show that the detection of the noise targets with maskers of a low fundamental frequency is determined mainly by the sharpest temporal resolution of the auditory system in the high-frequency region. For maskers of a high fundamental frequency the detection is determined mainly by the sharpest spectral resolution in the low-frequency region. Noise targets with global random phase and amplitude are relatively more difficult to detect than those produced by a local randomization. Local random phase noise targets are generally more detectable than those produced by local amplitude randomization. The relative importance of phase and magnitude spectra in the Fourier transform coding is strongly dependent on the fundamental frequency of the vowel sounds and the window size used in the short-time Fourier analysis.

Auditory Perception↗

Neural model for physiological responses to frequency and amplitude transitions uncovers topographical order in the auditory cortex.

We characterize primary auditory cortex (AI) units using a neural model for the detection of frequency and amplitude transitions. The model is a generalization of a model for the detection of amplitude transition. A set of neurons, tuned in the spectrotemporal domain, is created by means of neural delays and frequency filtering. The sensitivity of the model to frequency and amplitude transitions is achieved by applying a 2-dimensional rotatable receptive field to the set of spectrotemporally tuned neurons. We evaluated the model using data recorded in AI of anesthetized ferrets. We show that the model is able to fit the responses of AI units to variety of stimuli, including single tones, delayed 2-tone stimuli and various frequency-modulated tones, using only a small number of parameters. Furthermore, we show that the topographical order in maps of the model parameters is higher than in maps created from response indices extracted directly from the responses to any single stimulus. These results suggest a possible ordered organization of a simple rotatable spectrotemporal receptive field in the mammalian AI.

Acoustic Stimulation↗