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PubMed2003

Time course of loudness recalibration: implications for loudness enhancement.

Loudness recalibration, the effect of a relatively loud 2500-Hz recalibrating tone on the loudness of a relatively soft 2500-Hz target tone, was measured as a function of the interstimulus interval (ISI) between them. The loudness of the target tone, assessed by a 500-Hz comparison tone, declined when the ISI equaled or exceeded about 200 ms and leveled off at an ISI of about 700 ms. Notably, the target tone's loudness did not change significantly at very short ISIs (< 150 ms). The latter result is incompatible with the literature reporting loudness enhancement in this time window, but is compatible with the suggestion made by Scharf, Buus, and Nieder [J. Acoust. Soc. Am. 112, 807-810 (2002)] that early measurements of enhancement were contaminated by the influence of the recalibrating tone on the comparison tone when the two shared the same frequency. In a second experiment the frequency of the comparison tone was changed to 2500 Hz and the results of a loudness enhancement paradigm was successfully predicted from the time course of recalibration obtained in experiment 1.

Acoustic Stimulation↗
PubMed1991

Dependence of binaural loudness summation on interaural level differences, spectral distribution, and temporal distribution.

Loudness of interaurally correlated narrow- and broadband noises was investigated using a loudness estimation paradigm (with two anchors) presented via headphones. Throughout the experiments (most performed by 12 subjects), the results from both anchors agreed very well. In the first experiment, third-octave-band noises centered around 250, 710, or 2000 Hz, as well as broadband red (-10 dB/oct), pink (-3 dB/oct), and blue (+10 dB/oct) noises, with interaural level differences of delta L = 0, 4, 10, 20, and infinity dB, were presented as test signals while the same sound presented monaurally or diotically served as anchor. The binaurally summed loudness at delta L = 0 dB was found to be larger than the loudness of a monaural signal of the same SPL by a factor of about 1.5 and decreased with increasing delta L. No dependence of this behavior on frequency, level, or spectral shape was found. In a second experiment, abutting frequency bands of varying width were alternately presented to the subject's left and right ears with the overall spectrum encompassing the whole audio range. The binaural loudness was larger for fewer but broader frequency bands. In a third experiment, uniform exciting noise was switched between the two ears at various speeds. Increasing the switching frequency gave rise to an increase in loudness of about 20%. All results are discussed from the viewpoint of the use of the standardized loudness meter. At this point, there is no evidence that any significant systematic errors due to single-channel evaluation (in contrast to the human two-channel processing) are made by measuring loudness using these meters.

Adult↗
PubMed1985

Effects of flanking noise bands on the rate of growth of loudness of tones in normal and recruiting ears.

Five subjects with unilateral cochlear hearing impairments and three normally hearing subjects made loudness matches between tones presented alternately to two ears, as a function of the intensity of the tone in the impaired ear (or the left ear of the normal subjects). The impaired ears showed recruitment; the rate of growth of loudness with increasing intensity was more rapid in the impaired ear than the normal ear. Presenting the tone in the impaired ear with two noise bands on either side of the tone frequency, at a fixed signal-to-noise ratio, did not abolish the recruitment. This suggests that recruitment is not caused by an abnormally rapid spread of excitation in the peripheral auditory system. At low signal-to-noise ratios, a continuous background noise reduced the loudness of the tone more than a noise gated with the tone, suggesting that the continuous noise induces adaptation to the tone. The noise had a greater effect on the loudness of the tone in normal ears than in impaired ears. It is possible that the loudness reduction of the tone in noise is mediated by suppression; suppression is weak or absent in impaired ears, and so the loudness reduction is smaller.

Aged↗
PubMed1987

The effect of cross-spectrum correlation on the detectability of a noise band.

An experiment was performed to study the interaction of two narrow-band noises having correlated temporal envelopes. The detection threshold of a 100-Hz-wide noise-band signal was measured at different center frequencies in the presence of a continuous 100-Hz-wide noise band having a center frequency of 1000 Hz. The two noise bands had either correlated or independent temporal envelopes. Measured signal detection thresholds are lower when the two noise bands are independent, but the magnitude of this difference is not a simple function of the frequency separation between the two noise bands.

Adult↗
PubMed1987

Temporal resolution in sensorineural hearing-impaired listeners.

Temporal masking curves were obtained from 12 normal-hearing and 16 hearing-impaired listeners using 200-ms, 1000-Hz pure-tone maskers and 20-ms, 1000-Hz fixed-level probe tones. For the delay times used here (greater than 40 ms), temporal masking curves obtained from both groups can be well described by an exponential function with a single level-independent time constant for each listener. Normal-hearing listeners demonstrated time constants that ranged between 37 and 67 ms, with a mean of 50 ms. Most hearing-impaired listeners, with significant hearing loss at the probe frequency, demonstrated longer time constants (range 58-114 ms) than those obtained from normal-hearing listeners. Time constants were found to grow exponentially with hearing loss according to the function tau = 52e0.011(HL), when the slope of the growth of masking is unity. The longest individual time constant was larger than normal by a factor of 2.3 for a hearing loss of 52 dB. The steep slopes of the growth of masking functions typically observed at long delay times in hearing-impaired listeners' data appear to be a direct result of longer time constants. When iterative fitting procedures included a slope parameter, the slopes of the growth of masking from normal-hearing listeners varied around unity, while those from hearing-impaired listeners tended to be less (flatter) than normal. Predictions from the results of these fixed-probe-level experiments are consistent with the results of previous fixed-masker-level experiments, and they indicate that deficiencies in the ability to detect sequential stimuli should be considerable in hearing-impaired listeners, partially because of extended time constants, but mostly because forward masking involves a recovery process that depends upon the sensory response evoked by the masking stimulus. Large sensitivity losses reduce the sensory response to high SPL maskers so that the recovery process is slower, much like the recovery process for low-level stimuli in normal-hearing listeners.

Female↗
PubMed1990

Loudness growth in 1/2-octave bands (LGOB)--a procedure for the assessment of loudness.

In this paper, a method that has been developed for the assessment and quantification of loudness perception in normal-hearing and hearing-impaired persons is described. The method has been named LGOB, which stands for loudness growth in 1/2-octave bands. The method uses 1/2-octave bands of noise, centered at 0.25, 0.5, 1.0, 2.0, and 4.0 kHz, with subjective levels between a subject's threshold of hearing and the "too loud" level. The noise bands are presented to the subject, randomized over frequency and level, and the subject is asked to respond with a loudness rating (one of: VERY SOFT, SOFT, OK, LOUD, VERY LOUD, TOO LOUD). Subject responses (normal and hearing-impaired) are then compared to the average responses of a group of normal-hearing subjects. This procedure allows one to estimate the subject's loudness growth relative to normals, as a function of frequency and level. The results may be displayed either as isoloudness contours or as recruitment curves. In its present form, the measurements take less than 30 min. The signal presentation and analysis is done using a PC and a PC plug-in board having a digital to analog converter.

Adult↗
PubMed1997

Increment and decrement detection in sinusoids as a measure of temporal resolution.

Measuring thresholds for the detection of brief decrements in the level of a sinusoid is an established method of estimating auditory temporal resolution. Generally, a background noise is added to the stimulus to avoid the detection of the "spectral splatter" introduced by the decrement. Results are often described in terms of a temporal-window model, comprising a band-pass filter, a compressive nonlinearity, a sliding temporal integrator, and a decision device. In this study, thresholds for increments, as well as decrements, in the level of a 55 dB SPL, 4-kHz sinusoidal pedestal were measured as function of increment and decrement duration in the presence of a broadband background noise ranging in spectrum level from -20 to +20 dB SPL. Thresholds were also measured using a 55-dB, 8-kHz pedestal in the absence of background noise. Thresholds for decrements, in terms of the dB change in level (delta L), were found to be more dependent on duration than those for increments. Also, performance was found to be dependent on background-noise level over most levels tested. Neither finding is consistent with the predictions of the temporal-window model or other similar models of temporal resolution. The difference between increment and decrement detection was more successfully simulated by using a decision criterion based on the maximum slope of the temporal-window output.

Adult↗
PubMed1999

Detection of time- and bandlimited increments and decrements in a random-level noise.

The purpose of this study was to compare detection of increments and decrements occurring over limited regions of time and frequency within a 500-ms broadband (0-6000 Hz) noise. Three listeners tracked detection thresholds adaptively in a two-interval, two-alternative forced-choice task. Thresholds were measured for both increments and decrements in level [delta L = 10 log10(1 + delta N0/N0) dB, where N0 is the spectral power density of the noise] as a function of signal duration (T = 30-500 ms) for a range of signal bandwidths (W = 62-6000 Hz) that were logarithmically centered around 2500 Hz. Listeners were forced to rely on temporal- and spectral-profile cues for detection due to randomization of overall presentation level from interval to interval, which rendered overall energy an inconsistent cue. Increments were detectable for all combinations of W and T, whereas decrements were not consistently detectable for W < 500 Hz. Narrow-band decrements were not detectable due to spread of excitation from the spectral edges of the noise into the decrements. Increment and decrement thresholds were similar for W > or = 1000 Hz. Temporal- and spectral-integration effects were observed for both increments and decrements. The exceptions were for random-level conditions in which the signal matched the bandwidth or duration of the standard. A multicue decision process is described qualitatively to explain how the combination of temporal- and spectral-profile cues can produce temporal- and spectral-integration effects in the absence of overall-energy cues.

Adult↗
PubMed1999

Effects of frequency and duration on psychometric functions for detection of increments and decrements in sinusoids in noise.

Psychometric functions for detecting increments or decrements in level of sinusoidal pedestals were measured for increment and decrement durations of 5, 10, 20, 50, 100, and 200 ms and for frequencies of 250, 1000, and 4000 Hz. The sinusoids were presented in background noise intended to mask spectral splatter. A three-interval, three-alternative procedure was used. The results indicated that, for increments, the detectability index d' was approximately proportional to delta I/I. For decrements, d' was approximately proportional to delta L. The slopes of the psychometric functions increased (indicating better performance) with increasing frequency for both increments and decrements. For increments, the slopes increased with increasing increment duration up to 200 ms at 250 and 1000 Hz, but at 4000 Hz they increased only up to 50 ms. For decrements, the slopes increased for durations up to 50 ms, and then remained roughly constant, for all frequencies. For a center frequency of 250 Hz, the slopes of the psychometric functions for increment detection increased with duration more rapidly than predicted by a "multiple-looks" hypothesis, i.e., more rapidly than the square root of duration, for durations up to 50 ms. For center frequencies of 1000 and 4000 Hz, the slopes increased less rapidly than predicted by a multiple-looks hypothesis, for durations greater than about 20 ms. The slopes of the psychometric functions for decrement detection increased with decrement duration at a rate slightly greater than the square root of duration, for durations up to 50 ms, at all three frequencies. For greater durations, the increase in slope was less than proportional to the square root of duration. The results were analyzed using a model incorporating a simulated auditory filter, a compressive nonlinearity, a sliding temporal integrator, and a decision device based on a template mechanism. The model took into account the effects of both the external noise and an assumed internal noise. The model was able to account for the major features of the data for both increment and decrement detection.

Adult↗
PubMed1998

Codes for sound-source location in nontonotopic auditory cortex.

We evaluated two hypothetical codes for sound-source location in the auditory cortex. The topographical code assumed that single neurons are selective for particular locations and that sound-source locations are coded by the cortical location of small populations of maximally activated neurons. The distributed code assumed that the responses of individual neurons can carry information about locations throughout 360 degrees of azimuth and that accurate sound localization derives from information that is distributed across large populations of such panoramic neurons. We recorded from single units in the anterior ectosylvian sulcus area (area AES) and in area A2 of alpha-chloralose-anesthetized cats. Results obtained in the two areas were essentially equivalent. Noise bursts were presented from loudspeakers spaced in 20 degrees intervals of azimuth throughout 360 degrees of the horizontal plane. Spike counts of the majority of units were modulated >50% by changes in sound-source azimuth. Nevertheless, sound-source locations that produced greater than half-maximal spike counts often spanned >180 degrees of azimuth. The spatial selectivity of units tended to broaden and, often, to shift in azimuth as sound pressure levels (SPLs) were increased to a moderate level. We sometimes saw systematic changes in spatial tuning along segments of electrode tracks as long as 1.5 mm but such progressions were not evident at higher sound levels. Moderate-level sounds presented anywhere in the contralateral hemifield produced greater than half-maximal activation of nearly all units. These results are not consistent with the hypothesis of a topographic code. We used an artificial-neural-network algorithm to recognize spike patterns and, thereby, infer the locations of sound sources. Network input consisted of spike density functions formed by averages of responses to eight stimulus repetitions. Information carried in the responses of single units permitted reasonable estimates of sound-source locations throughout 360 degrees of azimuth. The most accurate units exhibited median errors in localization of <25 degrees, meaning that the network output fell within 25 degrees of the correct location on half of the trials. Spike patterns tended to vary with stimulus SPL, but level-invariant features of patterns permitted estimates of locations of sound sources that varied through 20-dB ranges. Sound localization based on spike patterns that preserved details of spike timing consistently was more accurate than localization based on spike counts alone. These results support the hypothesis that sound-source locations are represented by a distributed code and that individual neurons are, in effect, panoramic localizers.

Action Potentials↗
PubMedDate not supplied

Auditory brainstem potentials in uraemia.

Evoked response audiometry was carried out to assess the viability of the auditory pathway in haemodialysed patients. The latency of the waves III and V and I-V interpeak latencies were significantly longer in the renal patients compared to the control group. The I-V interpeak latency was longer in 8 of our 13 patients than the upper limit (4.38 ms) in our laboratory. The possible cause for the central auditory dysfunction may be multifactorial, including the effect of metastatic calcifications, repeated occurrence of disequilibrium syndrome, or some small, molecular, toxic, metabolic substance. The significance of the different factors may vary among different haemodialysis centres.

Adult↗
PubMed1990

Vestibular recruitment in Meniere's disease.

The aim of this study was to search for vestibular recruitment in a sample of patients with Meniere's disease. Recruitment was defined as an abnormal growth of response with increasing stimulus intensity. Twenty-nine patients were tested with sinusoidal rotation of three different magnitudes at four different frequencies. We also searched for auditory recruitment in each patient via tests of auditory brain stem responses, acoustic reflexes, and loudness balance and discomfort level. Analysis of vestibular responses indicated, on average, a linear relationship between stimulus magnitude and response magnitude, ie, doubling the stimulus magnitude resulted in twice the response magnitude. Meniere's patients did not yield results significantly different (although they were more variable) from those of the normal subjects. The vestibular responses of patients with auditory recruitment did not differ systematically from those of patients without auditory recruitment. We conclude that vestibular recruitment, if it exists in patients with Meniere's disease, is not demonstrated by sinusoidal rotational testing.

Adult↗
PubMed1996

The growing-louder effect in short diotic stimuli.

Previous evidence from short monotic stimuli shows that a steady stimulus is perceived as growing louder; to be perceived as steady, the intensity of the stimulus must decrease. In the present study, 10 subjects heard a sequence of diotic tonal stimuli. Each stimulus lasted 1.5 sec. and increased, decreased, or remained steady in intensity; initial intensity was 40 dB SPL and carrier frequency was 1 kHz. Subjects made forced binary responses of "growing louder" or "growing softer" to each stimulus. Confirming the evidence from monotic stimuli, the mean value of changing intensity eliciting equal numbers of both responses was negative. Possible explanations for this growing-louder effect reside in (a) the percussive nature of many natural sounds and (b) selective responding to approaching sound-sources.

Adult↗
PubMedDate not supplied

A computer-controlled binaural balance test.

The commonly used ABLB procedure (Alternate Binaural Loudness Balance) is strongly influenced by two psychological factors: the consistency of the referred side and the increase in intensity in equal stages on this side. To avoid this influence, side and intensity have to be randomized. The test has therefore been subjected to computer control and the results are continuously checked as to their significance. 26 patients with suspected inner-ear disturbance showed a significant relative recruitment; by contrast, in not one of 14 normal-hearing persons was the result positive. This test takes no longer than the conventional procedure.

Computers↗
PubMed1979

Cochleo-vestibular correlations in Meniere's disease.

The cochlear and vestibular functions were investigated in a sample of 36 patients with unilateral Meniere's disease. Caloric reactions and hearing thresholds were compared separately at several frequencies. A topodiagnostic relationship between the cochlear and vestibular function was discovered. Using four qualitative categories, a significantly high correlation was obtained between the basal hearing loss (4000 Hz) and unilateral weakness, whereas no correlation was obtained when evaluating the more apical hearing loss (lower frequencies 250-1 000 Hz). A normal caloric reaction can be reasonably expected in cases of unilateral Meniere's disease if the hearing loss is less than approx. 40 dB HL at 4 000 Hz.

Adolescent↗
PubMedDate not supplied

The loudness of tinnitus.

Paradoxically, measurements of the loudness of tinnitus indicate that the noise is not a very loud one, yet many persons experiencing it report severe distress. It has been suggested that either loudness has not been measured correctly or that some other factor such as recruitment may be involved. These aspects were investigated, with the following results: (1) the loudness levels obtained for two methods of measuring the loudness of tinnitus differed significantly with the proposed method yielding measures of greater magnitude without exception; (2) recruitment was evidenced for all subjects. On the basis of the results the following conclusions seem justified: (1) the loudness of tinnitus may be more intense than previously reported; (2) the proposed method for measuring the loudness of tinnitus appears to be a more valid measurement than the traditional method.

Adult↗