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PubMed2001

The feasibility of maximum length sequences to reduce acquisition time of the middle latency response.

Maximum length sequences (MLS) have been used to improve the signal-to-noise ratio (SNR) of otoacoustic emissions [Thornton, J. Acoust. Soc. Am. 94, 132-136 (1993)] and the auditory brainstem response [Thornton and Slaven, Br. J. Audiol. 27, 205-210 (1993)]. By implication, a shorter recording time would be required to give equal signal-to-noise ratio (SNR). This study aimed to establish whether it is also possible to improve the SNR of the auditory-evoked potential termed the middle latency response (MLR) using maximum length sequences (MLS). Recordings of 180 s each were made using a conventional recording rate and MLS rates of 42, 89, and 185 clicks/s. Three different stimulus intensities were used in the range 30 to 70 dB nHL. The rate of 89 clicks/s was found to produce most improvement in SNR for both the Na-Pa region of the MLR and the Na-Pb region. This improvement in SNR using MLS implies that an MLS rate of 89 clicks/s would produce a fourfold reduction in recording time for equal SNR over conventional recording for the Pa-Nb region of the MLR at a stimulus intensity of 70 dB nHL. The latency of the Nb wave was found to reduce significantly using MLS. An MLR could not be recorded from every subject in this study, but more subjects had an identifiable response for MLS than for conventional recordings. Use of MLS to record the MLR appears to offer the potential for reduction in test time and better wave identification.

Adult↗
PubMed2001

Neural representation of sound amplitude by functionally different auditory receptors in crickets.

The physiological characteristics of auditory receptor fibers (ARFs) of crickets, a model system for studying auditory behaviors and their neural mechanisms, are investigated. Unlike auditory receptor neurons of many animals, cricket ARFs fall into three distinct populations based on characteristic frequency (CF) [Imaizumi and Pollack, J. Neurosci. 19, 1508-1516 (1999)]. Two of these have CFs similar to the frequency component of communication signals or of ultrasound produced by predators, and a third population has intermediate CF. Here, sound-amplitude coding by ARFs is examined to gain insights to how behaviorally relevant sounds are encoded by populations of receptor neurons. ARFs involved in acoustic communication comprise two distinct anatomical types, which also differ in physiological parameters (threshold, response slope, dynamic range, minimum latency, and sharpness of tuning). Thus, based on CF and anatomy, ARFs comprise four populations. Physiological parameters are diverse, but within each population they are systematically related to threshold. The details of these relationships differ among the four populations. These findings open the possibility that different ARF populations differ in functional organization.

Animals↗
PubMed2001

Monaural masking release in random-phase and low-noise noise.

Two masking-release paradigms thought to involve across-channel processing are comodulation masking release (CMR) and profile analysis. Similarities between these two paradigms were explored by comparing signal detection in maskers that varied only in degree of envelope fluctuation. The narrow-band-noise maskers were 10 Hz wide and their envelope fluctuations were manipulated using the low-noise noise algorithm of Pumplin [J. Acoust. Soc. Am. 78, 100-104 (1985)]. Masking conditions included the classic CMR conditions of an on-frequency band, multiple (five) incoherent bands, or multiple coherent bands. Detection was compared using both random-phase noise (RPN) and low-noise noise (LNN) maskers. In one set of conditions, the signal was identical to the on-frequency masker, yielding an intensity discrimination task. Conditions that included RPN maskers and tonal signals resembled the classic CMR paradigm, whereas conditions including LNN and noise signals more closely resembled the classic profile analysis paradigm. Other conditions may be considered hybrids. This combination of conditions provided a wide variety of within- and across-channel cues for detection. The results suggest that CMR and profile analysis could be based upon the same set of stimulus cues and perhaps the same perceptual processes.

Adult↗
PubMed2001

Gap detection for similar and dissimilar gap markers.

Detection thresholds for temporal gaps between markers of dissimilar frequency are usually elevated with respect to thresholds for gaps between markers of similar frequency. Because gaps between markers of dissimilar frequency represent both a spectrally based perceptual discontinuity as well as a temporal discontinuity, it is not clear what factors underlie the threshold elevation. This study sought to examine the effects of perceptual dissimilarities on gap detection. The first experiment measured gap detection for configurations of narrow-band gap markers comprised of pure tones, frequency-modulated tones, and amplitude-modulated tones. The results showed that gap thresholds for frequency-disparate pure-tone markers were elevated with respect to isofrequency tonal markers, but that perceptual discontinuities between markers restricted to the same frequency region did not uniformly elevate threshold. The second experiment measured gap detection for configurations of markers where the leading and trailing markers could differ along the dimensions of bandwidth, duration, and pitch. The results showed that, in most cases, gap detection deteriorated when the bandwidth of the two markers differed, even when the spectral content of the narrower-band marker was completely subsumed by the spectral content of the wider-band marker. This finding suggests that gap detection is sensitive to spectral dissimilarity between markers in addition to spectral discontinuity. The effects of marker duration depended on the marker bandwidth. Pitch differences across spectrally similar markers had no effect.

Adult↗
PubMed2001

The effect of basilar-membrane nonlinearity on the shapes of masking period patterns in normal and impaired hearing.

Masking period patterns (MPPs) were measured in listeners with normal and impaired hearing using amplitude-modulated tonal maskers and short tonal probes. The frequency of the masker was either the same as the frequency of the probe (on-frequency masking) or was one octave below the frequency of the probe (off-frequency masking). In experiment 1, MPPs were measured for listeners with normal hearing using different masker levels. Carrier frequencies of 3 and 6 kHz were used for the masker. The probe had a frequency of 6 kHz. For all masker levels, the off-frequency MPPs exhibited deeper and longer valleys compared with the on-frequency MPPs. Hearing-impaired listeners were tested in experiment 2. For some hearing-impaired subjects, masker frequencies of 1.5 kHz and 3 kHz were paired with a probe frequency of 3 kHz. MPPs measured for listeners with hearing loss had similar shapes for on- and off-frequency maskers. It was hypothesized that the shapes of MPPs reflect nonlinear processing at the level of the basilar membrane in normal hearing and more linear processing in impaired hearing. A model assuming different cochlear gains for normal versus impaired hearing and similar parameters of the temporal integrator for both groups of listeners successfully predicted the MPPs.

Auditory Perception↗
PubMed2001

Infants' sensitivity to broadband noise.

Infants have higher pure-tone thresholds than adults. One explanation is that infants do not adopt the frequency-selective listening strategy that adults use when detecting tones. In contrast to other models of infants' immature sensitivity, the listening strategy account predicts that infants will be more sensitive to broadband sounds, relative to adults. Infants 7-9 months old were tested in two experiments to examine their sensitivity to broadband noise. Unmasked and masked thresholds for a 1000-Hz tone and for broadband noise were estimated adaptively for infants and adults using an observer-based behavioral procedure. The difference between infants and adults in unmasked threshold were 14 and 7 dB for tones and noise, respectively. The difference between infants and adults in masked threshold were 10 and 5 dB for tones and noise, respectively. Psychometric functions for detection of broadband noise were also obtained from some infants and adults. Infants' psychometric functions were similar to those obtained in tone detection with shallower slopes and lower upper asymptotes than adults'. This suggests that the relative improvement in infants' threshold for broadband noise is not due to greater attentiveness to the noise. A model of infants' sound detection invoking inattentiveness, listening strategy, and an unspecified source of internal noise may account for the characteristics of the infant psychometric function.

Adolescent↗
PubMed2001

A computational algorithm for computing nonlinear auditory frequency selectivity.

Computational algorithms that mimic the response of the basilar membrane must be capable of reproducing a range of complex features that are characteristic of the animal observations. These include complex input output functions that are nonlinear near the site's best frequency, but linear elsewhere. This nonlinearity is critical when using the output of the algorithm as the input to models of inner hair cell function and subsequent auditory-nerve models of low- and high-spontaneous rate fibers. We present an algorithm that uses two processing units operating in parallel: one linear and the other compressively nonlinear. The output from the algorithm is the sum of the outputs of the linear and nonlinear processing units. Input to the algorithm is stapes motion and output represents basilar membrane motion. The algorithm is evaluated against published chinchilla and guinea pig observations of basilar membrane and Reissner's membrane motion made using laser velocimetry. The algorithm simulates both quantitatively and qualitatively, differences in input/output functions among three different sites along the cochlear partition. It also simulates quantitatively and qualitatively a range of phenomena including isovelocity functions, phase response, two-tone suppression, impulse response, and distortion products. The algorithm is potentially suitable for development as a bank of filters, for use in more comprehensive models of the peripheral auditory system.

Algorithms↗
PubMed2001

Reconciling frequency selectivity and phase effects in masking.

The effects of auditory frequency selectivity and phase response on masking were studied using harmonic tone complex maskers with a 100-Hz fundamental frequency. Positive and negative Schroeder-phase complexes (m+ and m-), were used as maskers and the signal was a long-duration sinusoid. In the first experiment, thresholds for signal frequencies of 1 and 4 kHz were measured as a function of masker bandwidth and number of components. A large difference in thresholds between the m+ and m- complexes was found only when masker components were presented ipsilateral to the signal over a frequency range wider than the traditional critical band, regardless of the absolute number of components. In the second experiment, frequency selectivity was measured in harmonic tone complexes with fixed or random phases as well as in noise, using a variant of the notched-noise method with a fixed masker level. The data showed that frequency selectivity is not affected by masker type, indicating that the wide listening bandwidth suggested by the first experiment cannot be ascribed to broader effective filters in complex-tone maskers than in noise maskers. The third experiment employed a novel method of measuring frequency selectivity, which has the advantage that the overall level at the input and the output of the auditory filter remains roughly constant across all conditions. The auditory filter bandwidth measured using this method was wider than that measured in the second experiment, but may still be an underestimate, due to the effects of off-frequency listening. The data were modeled using a single-channel model with various initial filters. The main findings from the simulations were: (1) the magnitude response of the Gammatone filter is too narrow to account for the phase effects observed in the data; (2) none of the other filters currently used in auditory models can account for both frequency selectivity and phase effects in masking; (3) the Gammachirp filter can be made to provide a good account of the data by altering its phase response. The final conclusion suggests that masker phase effects can be accounted for with a single-channel model, while still remaining consistent with measures of frequency selectivity: effects that appear to involve broadband processing do not necessarily require across-channel mechanisms.

Acoustic Stimulation↗
PubMed2002

Relations among early postexposure noise-induced threshold shifts and permanent threshold shifts in the chinchilla.

Threshold shifts (TS) were measured at various times following a wide variety of noise exposures on over 900 chinchillas. An analysis of postexposure TS measures and noise-induced permanent threshold shift (PTS) showed that, across audiometric test frequency, there was a consistent relation between these variables of the form PTS (dB) = alpha(e(TS/beta) - 1), where, for a given test frequency, alpha (dB) and beta (dB) are constants. TSs were measured immediately following exposure (TS0), 24 h after exposure (TS24), and at several intermediate times in order to estimate the maximum TS (TSmax). Correlation between TS and PTS at the various test frequencies was highest for TS24. An analysis of the 90th-percentile PTS showed a linear growth of PTS with TS24 of approximately 0.7 dB PTS/dB TS24. These data provide some support, in the chinchilla model, for a variation of the three postulates originally presented by Kryter et al. [J. Acoust. Soc. Am. 39, 451 (1966)]. Specifically: (i) TS24 is a consistent measure of the effects of a traumatic noise exposure. (ii) All exposures that produce a given TS24 will be equally hazardous. (iii) Noise-induced PTS in the most susceptible animals, following many years of exposure, is approximately equal to (0.7)TS24 measured after an 8-h exposure to the same noise.

Animals↗
PubMed2002

Discrimination of sound source velocity in human listeners.

The ability of six human subjects to discriminate the velocity of moving sound sources was examined using broadband stimuli presented in virtual auditory space. Subjects were presented with two successive stimuli moving in the frontal horizontal plane level with the ears, and were required to judge which moved the fastest. Discrimination thresholds were calculated for reference velocities of 15, 30, and 60 degrees/s under three stimulus conditions. In one condition, stimuli were centered on 0 degrees azimuth and their duration varied randomly to prevent subjects from using displacement as an indicator of velocity. Performance varied between subjects giving median thresholds of 5.5, 9.1, and 14.8 degrees/s for the three reference velocities, respectively. In a second condition, pairs of stimuli were presented for a constant duration and subjects would have been able to use displacement to assist their judgment as faster stimuli traveled further. It was found that thresholds decreased significantly for all velocities (3.8, 7.1, and 9.8 degrees/s), suggesting that the subjects were using the additional displacement cue. The third condition differed from the second in that the stimuli were "anchored" on the same starting location rather than centered on the midline, thus doubling the spatial offset between stimulus endpoints. Subjects showed the lowest thresholds in this condition (2.9, 4.0, and 7.0 degrees/s). The results suggested that the auditory system is sensitive to velocity per se, but velocity comparisons are greatly aided if displacement cues are present.

Adult↗
PubMed2002

Auditory filter shapes for the bottlenose dolphin (Tursiops truncatus) and the white whale (Delphinapterus leucas) derived with notched noise.

Auditory filter shapes were estimated in two bottlenose dolphins (Tursiops truncatus) and one white whale (Delphinapterus leucas) using a behavioral response paradigm and notched noise. Masked thresholds were measured at 20 and 30 kHz. Masking noise was centered at the test tone and had a bandwidth of 1.5 times the tone frequency. Half-notch width to center frequency ratios were 0, 0.125, 0.25, 0.375, and 0.5. Noise spectral density levels were 90 and 105 dB re: 1 microPa2/Hz. Filter shapes were approximated using a roex(p,r) function; the parameters p and r were found by fitting the integral of the roex(p,r) function to the measured threshold data. Mean equivalent rectangular bandwidths (ERBs) calculated from the filter shapes were 11.8 and 17.1% of the center frequency at 20 and 30 kHz, respectively, for the dolphins and 9.1 and 15.3% of the center frequency at 20 and 30 kHz, respectively, for the white whale. Filter shapes were broader at 30 kHz and 105 dB re: 1 microPa2/Hz masking noise. The results are in general agreement with previous estimates of ERBs in Tursiops obtained with a behavioral response paradigm.

Animals↗
PubMed2002

Changes in auditory sensitivity with depth in a free-diving California sea lion (Zalophus californianus).

All current data on underwater hearing in pinnipeds are based on tests conducted in small tanks, and may not accurately represent the auditory functioning of free-ranging animals, especially if hearing sensitivity changes with water depth. Underwater auditory thresholds were determined for a California sea lion at depths ranging from 10 to 100 meters. The following results were obtained: (1) False alarm probabilities (responding in the absence of a signal) decreased significantly with depth, indicating that the sea lion adopted a more conservative response criterion in deeper water. (2) Hearing sensitivity generally worsened with depth. (3) There was a significant interaction between depth and frequency, the depth effect being most pronounced at 10 kHz and reversing at 35 kHz. Increasing pressure related to diving probably alters the impedance characteristics of the pinniped ear, in particular affecting the size of the middle-ear air space via expansion of cavernous tissue in the middle-ear cavity. These results show that the middle ear plays a functional role in underwater sound detection in sea lions. However, contrary to previous speculation, the presence of cavernous tissue in the sea lion middle ear does not appear to enhance sensitivity at depth.

Animals↗
PubMed2002

Detection of static and dynamic changes in interaural correlation.

This study examines the relation between a static and a dynamic measure of interaural correlation discrimination: (1) the just noticeable difference (JND) in interaural correlation and (2) the minimum detectable duration of a fixed interaural correlation change embedded within a single noise-burst of a given reference correlation. For the first task, JNDs were obtained from reference interaural correlations of + 1, -1, and from 0 interaural correlation in either the positive or negative direction. For the dynamic task, duration thresholds were obtained for a brief target noise of +1, -1, and 0 interaural correlation embedded in reference marker noise of +1, -1, and 0 interaural correlation. Performance with a reference interaural correlation of +1 was significantly better than with a reference correlation of -1. Similarly, when the reference noise was interaurally uncorrelated, discrimination was significantly better for a target correlation change towards +1 than towards -1. Thus, for both static and dynamic tasks, interaural correlation discrimination in the positive range was significantly better than in the negative range. Using the two measures, the length of a binaural temporal window was estimated. Its equivalent rectangular duration (ERD) was approximately 86 ms and independent of the interaural correlation configuration.

Adult↗
PubMed2002

Direct-to-reverberant energy ratio sensitivity.

Although the ratio of direct-to-reverberant sound energy is known to be an important acoustic cue to sound source distance, human sensitivity to changes in this cue is largely unknown. Here, direct-to-reverberant energy discrimination thresholds were measured for six listeners using virtual sound source techniques that allow for convenient and precise control of this stimulus parameter. Four different types of source stimuli were tested: a 50 ms noise burst with abrupt onset/offset, a 300 ms duration noise burst with gradual onset/offset, a speech syllable, and an impulse. Over a range of direct-to-reverberant ratios from 0 to 20 dB, an adaptive 2AFC procedure (3-down, 1-up) was used to measure discrimination thresholds. For all stimuli, these thresholds ranged from 5 to 6 dB. A post hoc fitting procedure confirmed that slopes of the psychometric functions were homogeneous across stimulus conditions and listeners. These threshold results suggest that direct-to-reverberant energy ratio by itself provides only a course coding of sound source distance, because threshold values correspond to greater than 2-fold changes in physical distance for the acoustic environment under examination.

Acoustics↗
PubMed2003

Electrical field interactions in different cochlear implant systems.

The goal of this study was to evaluate electrical field interactions produced by the stimulation of different types of intracochlear electrodes in 12 adult subjects (three Ineraid, four Clarion S-Series, three S-Series with the electrode positioning system-EPS and two Clarion HiFocus-I with the EPS). Psychophysical measurements were conducted with biphasic stimuli (813 pulse per second, 153.8 micros/phase). "Perturbation" signals (300 ms) were applied to one electrode chosen at the middle of the array and their effects on detection thresholds of "probe" signals (30 ms) were measured on the neighbor basal electrode. Perturbation levels were set below the detection threshold of the perturbation electrode (-2 dB re threshold). Measurements were first conducted for simultaneous stimulation of the probe and of the perturbation electrodes, for monopolar for all subjects and for bipolar stimulus configurations for both Clarion HiFocus-I subjects. The tested Clarion electrodes did not present lower monopolar interactions than the Ineraid electrodes. Nevertheless, considering the shorter distance between electrodes for the Clarion than for the Ineraid, the tested Clarion electrodes might be more selective than the Ineraid. We did not find any significant monopolar electrical field-interaction differences between subjects who received the S-Series array with and without the EPS. We did not find lower interactions for both subjects who received the HiFocus-I array than for subjects who received the S-Series. Electrical field interactions were lower for bipolar than for monopolar configurations for both HiFocus-I subjects. A second set of measurements was conducted for nonsimultaneous stimulation similar to the one used in continuous interleaved sampling sound strategy. These measurements showed that interactions evaluated for simultaneous biphasic stimuli were larger than for nonsimultaneous stimulation.

Adult↗
PubMed2003

A Wiener filter approach to the binaural reproduction of stereo sound.

This paper considers authentic binaural reproduction with loudspeakers using cross-talk cancellation. A systematic time domain deconvolution method is presented using both stochastic and deterministic Wiener filters. This method has advantages in that the Wiener filter is inherently causal and stable so that no additional stabilization process, as generally required in the frequency domain methods, is needed. Errors involved in the authentic reproduction are classified into modeling, inverse, and repeatability errors. In addition, the reproduction error is used as the performance measure of a reproduction system. Finally, a series of monaural and binaural reproduction tests were conducted in an anechoic chamber using a PC based reproduction system with a soundcard by changing the length of the inverse filter used. Test results demonstrated that the performance was improved in proportion to the length of the filter used. The reproduction performance error and its test procedure presented here can be used for objectively assessing the performance of a subjective auditory perception test system.

Journal Article↗
PubMed2004

Annoyance caused by the sounds of a magnetic levitation train.

In a laboratory study, the annoyance caused by the passby sounds from a magnetic levitation (maglev) train was investigated. The listeners were presented with various sound fragments. The task of the listeners was to respond after each presentation to the question: "How annoying would you find the sound in the preceding period if you were exposed to it at home on a regular basis?" The independent variables were (a) the driving speed of the maglev train (varying from 100 to 400 km/h), (b) the outdoor A-weighted sound exposure level (ASEL) of the passbys (varying from 65 to 90 dB), and (c) the simulated outdoor-to-indoor reduction in sound level (windows open or windows closed). As references to the passby sounds from the maglev train (type Transrapid 08), sounds from road traffic (passenger cars and trucks) and more conventional railway (intercity trains) were included for rating also. Four important results were obtained. Provided that the outdoor ASELs were the same, (1) the annoyance was independent of the driving speed of the maglev train, (2) the annoyance caused by the maglev train was considerably higher than that caused by the intercity train, (3) the annoyance caused by the maglev train was hardly different from that caused by road traffic, and (4) the results (1)-(3) held true both for open or closed windows. On the basis of the present results, it might be expected that the sounds are equally annoying if the ASELs of the maglev-train passbys are at least 5 dB lower than those of the intercity train passbys. Consequently, the results of the present experiment do not support application of a railway bonus to the maglev-train sounds.

Adult↗