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PubMed1987

Spectral-shape discrimination. I. Results from normal-hearing listeners for stationary broadband noises.

This research is concerned with the ability of normal-hearing listeners to discriminate broadband signals on the basis of spectral shape. The signals were six broadband noises whose spectral shapes were modeled after the spectra of unvoiced fricative and plosive consonants. The difficulty of the discriminations was controlled by the addition of noise filtered to match the long-term speech spectrum. Two-interval discrimination measurements were made in which loudness cues were eliminated by randomizing (roving) the overall stimulus level between presentation intervals. Experimental results, examined as a function of intensity rove width, stimulus duration, and stimulus pair, were related to the predictions of a simple filter-bank model whose fitting parameter provides an estimate of internal noise. Most results, with the notable exception of duration effects, were predicted by the model. Estimates of internal noise in each frequency channel averaged roughly 7 dB for long-duration stimuli and 13 dB for short-duration stimuli. Results and predictions are compared to results of other studies concerned with the discrimination of spectral shape.

Humans↗
PubMed1987

The effect of impulse intensity and the number of impulses on hearing and cochlear pathology in the chinchilla.

Forty-one chinchillas, divided into seven groups, were exposed to 1, 10, or 100 noise impulses (one every 3s) having peak intensities of 131, 135, 139, or 147 dB. Hearing thresholds were measured in each animal before and after exposure using an avoidance conditioning procedure; a surface preparation of the cochlear sensory epithelia was performed approximately 90 days after exposure. There was generally an orderly relation between the amount of permanent threshold shift and the severity of exposure, and a general agreement between averaged histological data and the audiometric data. For the impulses used in this study, there is a range of intensities which is bounded on the high side by the intensity which just produces injury with single impulse exposures and bounded on the low side by a critical intensity below which the injury potential drops precipitously with a reduction of impulse intensity. This region is only about 10-15 dB wide for the exposure conditions of this experiment. Within this region, the threshold of injury is a constant total energy; i.e., 10-dB change of intensity implies a tenfold change in the number of impulses for threshold injury. Detailed relations between temporary and permanent threshold shift, cochlear pathology, and exposure variables are discussed, as are the implications of these data to the development of exposure criteria.

Animals↗
PubMed1987

Correlation between time functions of sound pressure, masking, and OAE suppression.

Periodic sound-pressure time functions with frequency components below 50 Hz were used to measure within their period (a) the temporal course of masking, called a masking-period pattern (MPP), and (b) the temporal course of suppression of delayed evoked otoacoustic emissions, called a suppression-period pattern (SPP). Three different time functions were used: an alternating Gaussian impulse, its first integral, and its second integral. In each case, the course of the SPP is a mirror image of that of the MPP: Small masking corresponds to small suppression, while strong masking coincides with almost total suppression. Since otoacoustic emissions are assumed to have their origin in the inner ear, it can be argued that simultaneous masking, an effect including central processing, is very strongly based on peripheral processes located in the cochlea. Both MPP and SPP are closely related to the second derivative of the sound-pressure time function.

Humans↗
PubMed1987

Tone-burst-evoked otoacoustic emissions from normal-hearing subjects.

Tone-burst-evoked otoacoustic emissions were measured as a function of tone-burst sound pressure level and frequency in normally hearing ears. Although the spectral and temporal properties varied across individual ears, there was a close correspondence between stimulus and response spectra. Both the spectral and latency characteristics of tone-burst-evoked emissions are consistent with the hypothesis that they are generated at sites along the cochlear partition corresponding to their frequency.

Acoustic Stimulation↗
PubMed1987

Binaural versus monaural loudness: supersummation of tone partially masked by noise.

A series of three experiments used the method of magnitude estimation to examine binaural summation of the loudness of a 1000-Hz tone heard in the quiet and against various backgrounds of masking noise. In the quiet, binaural loudness as measured in sones, is twice monaural loudness. Two conditions of noise masking acted to increase the ratio of binaural/monaural loudness in sones above 2:1--that is, to produce supersummation. (1) When tone was presented to both ears, but masking noise to just one ear (dichotic stimulation), the loudness of the binaural tone was 30%-35% greater than the sum of the loudness of the monaural components. This increase in summation provides a suprathreshold analog to increases in threshold sensitivity observed with dichotic stimulation (masking-level differences). (2) Supersummation was also evident when tone and noise alike were presented to both ears (diotic stimulation); here, the binaural tone's loudness was 10%-25% greater than the sum of the monaural components. The increase in summation with diotic stimulation may be related to the characteristics of binaural summation of the noise masker itself.

Dominance, Cerebral↗
PubMed1987

Comparative learning of pitch and loudness identification.

This study investigated possible similarities between the ability to identify pitches and the ability to identify loudnesses. Systematic training of musically naive subjects indicated that frequency identification performance improves at about the same rate as intensity identification performance. Examination of frequency and intensity identification behavior of musically trained subjects showed that their ability to code pitch information efficiently does not generalize to an ability to encode loudness information more efficiently than untrained subjects. Intensity identification training curves of musically trained and untrained subjects are similar, but final performance levels are below frequency identification performance levels exhibited by musically trained subjects, especially those with absolute pitch.

Discrimination Learning↗
PubMed1987

Response dynamics of goldfish saccular fibers: effects of stimulus frequency and intensity on fibers with different tuning, sensitivity, and spontaneous activity.

The effects of stimulus frequency and intensity on response patterns (PST histograms) to tone burst stimulation were examined in differently tuned saccular fibers of the goldfish. In addition, the sensitivity of these fibers to amplitude-modulated (AM) signals of different carrier frequencies was measured. The response patterns evoked by unmodulated signals were a complex function of tuning, spontaneous activity and sensitivity of the fiber, and the frequency and intensity of the signal. Frequency-dependent response patterns were found in low-frequency fibers with best frequencies (BF) below 200 Hz. Responses in these fibers ranged from tonic to phasic in nonspontaneous fibers and included more complex patterns in spontaneously active fibers, such as suppression of evoked activity below spontaneous levels. Midfrequency fibers (BF = 500-600 Hz) showed responses similar to those in low-frequency fibers, but with less dependence on frequency. In contrast, both high-frequency (BF = 800-1000 Hz) and wideband, untuned fibers showed frequency-invariant patterns of adaptation. High-frequency fibers were equally sensitive to AM signals at all frequencies tested. The sensitivity of low-frequency fibers to AM, however, increased as a function of carrier frequency and corresponded to the degree of adaptation in response to unmodulated tones. In general, the AM sensitivity of a fiber could be predicted more by its pattern of response to unmodulated signals than by its tuning characteristics.

Acoustic Stimulation↗
PubMed1987

Transient masking and the temporal course of simultaneous tone-on-tone masking.

Previous studies have shown that threshold for a signal in tone-on-tone simultaneous masking is sometimes lower when the masker is continuous than when it is gated. Threshold may also decline as signal onset is delayed relative to the onset of a longer duration masker, though it may increase again near masker offset. In the present study, the level of a 1250-Hz sinusoidal masker was found which would just mask a 20-ms, 1000-Hz sinusoid presented at 10-dB sensation level (SL). Masker duration was 20 or 400 ms; in the latter case, the signal was presented in one of three temporal positions within the masker. The level of the 1250-Hz masker necessary to mask the signal was reduced, sometimes by as much as 20-25 dB, by a 20-ms, 500-Hz sinusoid (transient masker) presented at the times when the signal might occur, but at a level 30 dB below that at which it would mask the 10-dB SL signal. This suggests that, in the earlier studies, at least some of the elevation in threshold in the presence of a short-duration masker or at the beginning (or end) of a longer duration masker may have been due to the transient responses to the masker affecting detection of the signal, but not necessarily masking the signal in terms of excitation in the signal "channel."

Acoustic Stimulation↗
PubMed1987

Stimulus intensity and loudness recruitment: neural correlates.

An abnormally rapid rate of loudness growth for given increments in stimulus intensity is seen both in patients with cochlear pathology and in normal listeners under conditions of wide-spectrum noise masking. The phenomenological similarity between these psychophysical observations raises the question of whether a single mechanism, or set of mechanisms, underlies them. Recent neurophysiological studies in animals have addressed the effects of cochlear pathology and noise masking on the neural correlates of stimulus intensity in the central auditory nervous system. A comparison of the data presented in those studies reveals that there are sequelae of cochlear pathology seen in the discharges of auditory-nerve fibers that might reasonably be expected to contribute to a steepened loudness function. These sequelae are not seen at the same locus in normal animals studied with noise masking paradigms. Noise masking, however, may have effects on the tonal sensitivity of more central neurons that mimic some of the sequelae of cochlear pathology seen in the auditory nerve. These data suggest that the mechanisms underlying the two manifestations of recruitment may be quite different, one having a uniquely cochlear site, while the other reflects purely central processes.

Acoustic Stimulation↗
PubMed1988

Frequency selectivity in loudness adaptation and auditory fatigue.

An intermittent monaural tone may induce a decline in the loudness of a continuous tone presented to the same ear [Canévet et al., Br. J. Audiol. 17, 49-57 (1983)]. Two experiments studied the frequency selectivity of loudness adaptation induced in this manner. The method of successive magnitude estimations was used to measure the loudness of a monaural 84-s test tone before and after a single presentation of a 24-s inducer tone in the same ear. The first experiment shows that, for an inducing tone (500, 1000, or 3000 Hz) approximately 15 dB more intense than a test tone set to one of 21 different frequencies, adaptation is greatest when the two tones have the same frequency; with increasing difference between the test-tone and inducer frequencies, adaptation progressively declines. The second experiment measured frequency selectivity in the loudness reduction caused by a 1000-Hz inducer as a function of its level. As inducer level went from 75 to 95 dB (with test tone constant at 60 phons), selectivity passes progressively from the type seen in short-term or low-level fatigue (maximal for the 1000-Hz test tone) to a type seen in long-term or high-level fatigue (maximal for the 1000-Hz test tone) to a type seen in long-term or high-level fatigue (maximal at frequencies higher than that of the inducer or fatiguing tone). A common cochlear origin and a continuity between the mechanisms of ipsilaterally induced adaptation and high-level fatigue are suggested by the data.

Adaptation, Physiological↗
PubMed1988

Binaural summation and lateralization of transients: a combined analysis.

Subjects judged the loudness and the lateral position of dichotic transient signals, which were presented at equal and unequal levels, synchronously and asynchronously, to the two ears. Binaural loudness summation of clicks does not obey a law of linear addition: It is partial at low level and superadditive at high level. Supersummation is greater for interaurally delayed clicks than for coincidental ones. The relation between click loudness and sound pressure (over moderate SLs) can be described as a power function with a greater exponent for the binaural function. Lateral positions spread over a greater range for interaural level differences than for interaural time differences. The time-intensity trading ratio was greater than is typically reported for tones. When sound lateralization was induced by interaural time difference, but not by intensity difference, a virtually perfect negative correlation between loudness and extent of off-center displacement existed.

Attention↗
PubMed1988

Intensity discrimination, increment detection, and magnitude estimation for 1-kHz tones.

Intensity difference limens (DLs) were measured over a wide intensity range for 200-ms, 1-kHz gated tones and for 200-ms increments in continuous 1-kHz tones. Magnitude estimates also were obtained for the gated tones over a comparable intensity range. The discrimination data are in general agreement with those from earlier studies but they extend them by showing: (1) good discrimination for gated tones over at least a 115-dB dynamic range; (2) a slight increase in the relative DL (delta I/I) as intensity increases above 95 dB SPL; (3) smaller DLs for increments than for gated tones, with the difference approximately independent of intensity; (4) negligible "negative masking" when thresholds are expressed as intensity differences (delta I). For two of the three subjects, magnitude estimates do not conform to a single-exponent power law for suprathreshold intensities. Over the middle range of intensities where a single exponent is appropriate, the value of the exponent is less than 0.1 for all subjects.

Acoustic Stimulation↗
PubMed1988

The relation between loudness and intensity difference limens for tones in quiet and noise backgrounds.

Recent studies of the relation between loudness and intensity difference limens (DLs) suggest that, if two tones of the same frequency are equally loud, they will have equal relative DLs [R. S. Schlauch and C.C. Wier, J. Speech Hear. Res. 30, 13-20 (1987); J.J. Zwislocki and H.N. Jordan, J. Acoust. Soc. Am. 79, 772-780 (1986)]. To test this hypothesis, loudness matches and intensity DLs for a 1000-Hz pure tone in quiet and in a 40-dB SPL spectrum level broadband noise were obtained for four subjects with normal hearing. The DLs were obtained in both gated- and continuous-pedestal conditions. Contrary to previous reports, equally loud tones do not yield equal relative DLs at several midintensities in the gated condition and at many intensities in the continuous condition. While the equal-loudness, equal-relative-DL hypothesis is not supported by the data, the relation between loudness and intensity discrimination appears to be well described by a model reported by Houtsma et al. [J. Acoust. Soc. Am. 68, 807-813 (1980)].

Audiometry, Pure-Tone↗
PubMed1988

Detection, loudness, and discrimination of five-component tonal complexes differing in crest factor.

The detection, loudness, and discrimination performances of subjects with normal hearing were assessed using 3 five-component tonal complexes (1020-1100 Hz) with crest factors of 1.8, 2.6, and 3.2. The 3 five-component tonal complexes were: (1) equally detectable in broadband noise when presented at equal rms amplitude; (2) perceived as equally loud when presented at essentially equal rms amplitude; and (3) discriminable from one another when presented at equal loudness. The present data indicate that listeners can make discriminations on the basis of amplitude variations.

Acoustic Stimulation↗
PubMed1988

Speech masking. II: Simultaneous masking thresholds under "naturalistic" listening conditions.

This article investigates the role of listening conditions in determining thresholds for probe tones masked by natural speech. These thresholds are of interest because they are a sensitive probe of the activity profile, or spectrum, of sounds such as speech in the auditory system. Most human performance tests are carried out under highly artificial listening conditions, which may not reflect how people listen to speech in common listening environments. In this study, reference conditions (similar to minimal uncertainty listening conditions used in many performance tests) were compared to a "naturalistic" listening condition and to another, intermediate, condition. In the naturalistic listening condition, listeners did not know the frequency or the position of probe tones; additionally, they were required to attend to the semantic content of sentences. In the reference condition, listeners knew the frequency and position of probe tones masked by single syllables. Average thresholds were elevated by 4 dB in the naturalistic listening condition with respect to the reference condition, and thresholds tended to be elevated more for higher-frequency probe tones. The results provide previously unknown information about the resolution of speech sounds in the auditory system during speech comprehension.

Adolescent↗
PubMed1989

Noise susceptibility and immunity of phase locking in amphibian auditory-nerve fibers.

Recordings from auditory-nerve fibers in the anesthetized frog revealed that addition of broadband noise results in a reduction in the ability of a fiber to phase lock to a continuous pure tone. In particular, our results suggest that: (i) there is a threshold below which masking noise has little or no effect on vector strength (VS); then with increasing masking noise level, VS appears to decrease monotonically for all test frequencies (TFs); (ii) there exist subpopulations of auditory-nerve fibers in the frog for which the deterioration of phase locking to tones in wideband noise depends critically on the relationship of the TF to the fiber's CF. Specifically, in one subpopulation (43% of the fibers studied), the rate of VS decrease with increasing levels of masking noise is greater for CF tones than it is for TFs greater than CF. The net result is a "crossing" of the VS versus masking noise functions (e.g., Fig. 6); (iii) there exists a small subpopulation of amphibian papillar (a.p.) fibers for which the rate of VS decrease with increasing levels of masking noise is less for TFs less than CF than it is for CF tones (e.g., Fig. 5); (iv) there is a pronounced noise-induced phase lead for TFs greater than CF, whereas, for stimulus tones at or below CF, the preferred firing phase is nearly noise-level independent; (v) the remainder of the sample consists of fibers in which the VS-falloff rates appear to be test-frequency independent; (vi) addition of wideband masking noise to a CF tone, and increasing the CF-tone level in the absence of noise, produced (qualitatively) similar effects on the preferred firing phase of auditory-nerve fibers (e.g., Figs. 1 and 7). Thus amphibian auditory-nerve fibers appear to be energy detectors, i.e., exhibit phase shifts corresponding to the total energy within the filter passband defined by the frequency-threshold curve.

Animals↗
PubMed1989

Intensity discrimination of pulsed tones by the goldfish (Carassius auratus).

Intensity discrimination thresholds for 500-ms pure-tone bursts were measured as a function of frequency in the goldfish (Carassius auratus) using classical respiratory conditioning. At 55-dB sensation level (SL), thresholds range from 1.44-2.2 dB between 100 and 1600 Hz. There is not important effect of frequency on intensity discrimination. Thresholds at 35-dB SL average 0.7 dB higher than at 55-dB SL. This is a small difference in the context of the threshold variability. In intensity discrimination acuity, the goldfish is quantitatively similar to other vertebrates, including birds and mammals.

Acoustic Stimulation↗
PubMed1989

The measurement of loudness in individual children and adults by absolute magnitude estimation and cross-modality matching.

Twelve adults and 11 children (age range 4-7 years) performed absolute magnitude estimation of the apparent lengths of lines and the loudnesses of 1000-Hz tones as well as cross-modality matching between loudness and apparent line length. Consistent with the notion that children and adults have similar impressions of loudness, there were no major differences between the absolute magnitude estimation (AME) and cross-modality matching (CMM) data of the adults and children. A direct comparison between the exponents for loudness by AME and CMM was made when a correction factor was employed to eliminate the effects of idiosyncratic use of numbers from the AME exponents. The results support the hypothesis that, with proper instructions, both children and adults can judge stimuli on an absolute scale. Specifically, for 9 out of 12 adults and 9 out of 11 children, lines and tones assigned the same number in absolute magnitude estimation were judged to be subjectively equal in cross-modality matching.

Adult↗