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PubMed1993

Combined evaluation of interaural time and intensity differences: psychoacoustic results and computer modeling.

The physical and the psychophysical relationships between interaural time and intensity differences were studied for 24 frequency bands of critical bandwidth covering the full audio range. For the physical investigations a catalogue of outer ear impulse responses for 122 directions of the upper hemisphere was analyzed according to the combinations of interaural time and level differences found in each critical band. From these data curves of "natural combinations" of the interaural parameter differences were determined by the minimum square error method. In a psychoacoustical study it is shown that signals containing "natural" parameter combinations produce response patterns that differ from those produced when signals with contradictory interaural properties have been used. Finally an extension to the powerful binaural model of Lindemann [J. Acoust. Soc. Am. 80, 1608-1622 (1986)] is introduced, taking into account the results of the previous investigations.

Acoustic Stimulation↗
PubMed1994

Listeners' expectations about echoes can raise or lower echo threshold.

Echo threshold increases with exposure to redundant trains of stimuli. Three experiments were conducted to test the hypothesis that a change in the ongoing train would affect listeners' perception of the echo, but only if it signified an unusual change in room acoustics. The stimulus train was composed of 4-ms narrow-band noise bursts, with the leading sound from a loudspeaker placed 45 degrees left of midline and the lagging sound or simulated echo from 45 degrees right, delivered in an anechoic chamber. The lagging sound in the test noise, which followed the train after a 750-ms pause, came randomly from loudspeakers at 35 degrees or 55 degrees right, and the listener's task was to choose which position the echo came from on each trial. In experiment 1 the delay between onsets of the leading and lagging bursts was varied between train and test bursts, which simulated a sudden movement of the reflecting surface either toward the listener (if the delay of the test burst was shorter than the train) or away (if the delay was longer). In both cases listeners detected the echo's direction more easily, compared to trials when there was no change between train and test burst delays. In order to check whether any change between train and test bursts would increase echo discriminability, experiment 2 varied frequency and experiment 3 varied intensity. These variations were not expected to affect the echo's detectability because such changes signify that the original sound changed in these characteristics and the echo reflected these changes.(ABSTRACT TRUNCATED AT 250 WORDS)

Acoustic Stimulation↗
PubMed1983

Adaptive changes in firing rates in goldfish auditory fibers as related to changes in mean amplitude of excitatory postsynaptic potentials.

Relationship between the firing rate in the auditory fibers and the amplitude of the excitatory postsynaptic potentials (EPSPs) that trigger afferent impulses was investigated. The unitary EPSPs and spike potentials were extracellularly recorded from the goldfish large auditory fibers by means of a microelectrode placed close to the distal terminals. The relation between the firing rate and the amplitude of the EPSPs was studied using a variety of stimulus conditions. The firing probability of phase-locked impulses was linearly related to the mean amplitude of the EPSPs determined for the same time bins. The same linear relation was applicable for the firings elicited by different intensities of sound and observed at various times after onset and also for the firings produced by applying step increments in intensity. The threshold amplitude of the EPSPs required for initiation of afferent impulses was unchanged in these different situations. Random changes in the amplitude of successively evoked EPSPs were found to underlie the probabilistic nature of the sequence of afferent firings. The present results indicate that the per stimulus adaptation and incremental and decremental responses, as observed in the firing probability of afferent impulses, are largely attributable to adaptive changes in the mean amplitude of the evoked EPSPs and not to changes in excitability of the auditory fibers.

Adaptation, Physiological↗
PubMed1993

Auditory startle response in blind subjects.

Blindness is often associated with hypervigilance and arousal. The auditory startle response has been suggested as a measure of arousal. This study evaluated the auditory startle response of 10 blind individuals and 10 sighted controls who were exposed to a series of 15 1000-Hz, 95-db, 0-rise-time pure-tone stimuli, administered to both ears. The subjects' heart-rate, skin-conductance, and orbicularis-oculi-electromyogram responses to the tones were measured. Blind subjects did not differ from controls in the magnitude and in the habituation-rate of their responses. Results were interpreted as showing that blind persons' capacity for discriminative learning and for regulation of arousal is unimpaired. Task-related anxiety of blind persons should be differentiated from stimulus-related anxiety.

Acoustic Stimulation↗
PubMed1998

Divided attention between simultaneous auditory and visual signals.

Past studies of simultaneous attention to pairs of visual stimuli have used the "dual-task" paradigm to show that identification of the direction of a change in luminance, whether incremental or decremental, is "capacity-limited," while simple detection of these changes is governed by "capacity-free" processes. On the basis of that finding, it has been suggested that the contrast between identification and detection reflects different processes in the sensory periphery, namely the responses of magno- and parvocellular receptors. The present study questions that assertion and investigates the contribution of central processing in resource limitation by applying the dual task to a situation in which one stimulus is auditory and one is visual. The results are much the same as before, with identification demonstrating the tradeoff in performance generally attributed to a limited capacity but detection showing no loss compared with single-task controls. This implies that limitations on resources operate at a central level of processing rather than in the auditory and visual peripheries.

Adult↗
PubMed1991

Duration discrimination of filled and empty auditory intervals: cognitive and perceptual factors.

Adult subjects were presented with two auditory stimuli per trial, and their task was to decide which of the two was longer in duration. An adaptive psychophysical procedure was used. In Experiments 1, 2, and 4, the base duration was 50 msec, whereas in Experiment 3, the base duration was 1 sec. In Experiments 1, 2, and 4, it was found that filled intervals (continuous tones) were discriminated more accurately than empty intervals (with onset and offset marked by clicks). It was concluded that this difference was perceptual rather than cognitive in nature, since performance on filled and empty intervals was not affected by increasing cognitive load in a dual-task procedure (Experiment 2) but was affected by backward masking (Experiment 4). In contrast, the results of Experiment 3 showed that duration discrimination of filled auditory intervals of longer duration was cognitively influenced, since performance was impaired by increasing cognitive load. Implications for notions of perceptual processing and timing mechanism underlying differences in duration discrimination with filled and empty intervals are discussed.

Adult↗
PubMed1999

Loudness discrimination of speech signals spectrally shaped by a simulated hearing aid.

A discrimination task was used to assess changes in the loudness of speech that accompanied changes in the spectral tilt of a simulated hearing aid's frequency response. Band-limited (0.25-4 kHz) spondaic words were spectrally shaped at comparison tilt-factor values of -6, 0, and +6 dB per octave and delivered monaurally via insert earphone to each of 10 listeners with normal hearing (NH) and 15 listeners with mild-to-moderate sensorineural hearing impairment (HI). Results for the NH listeners indicated that loudness differences among the tilt factors were generally perceptible and that loudness judgments were highly transitive across different tilt-factor comparisons. Loudness differences were also perceptible to many of the HI listeners when they switched among tilt factors. The HI listeners' data showed some evidence of transitivity, but not so much as was shown by the NH listeners. Intersubject variability in the loudness judgments was found to be comparable for the two subject groups. Results of the study are discussed with regard to their implications for hearing aid fitting, with particular emphasis on the "parameter adjustment and selection" fitting procedure (J. Punch & R. Robb, 1992).

Adult↗
PubMed1983

Auditory brain-stem responses in infants with Down's syndrome.

Auditory brain-stem responses to clicks were recorded from 38 infants with Down's syndrome at the ages of 3, 6, and 12 months in an attempt to delineate age-dependent and intensity-dependent latency changes in this population. Comparisons were made with 35 normally developing infants at the same age levels. Significant wave V latency differences were observed between groups for both age and intensity, with the group with Down's syndrome showing, in general, shorter absolute wave V latency values across age and steeper latency functions across intensity. The implications of this study are as follows: (1) latency-intensity curves for normally developing infants will not serve adequately as normative values for infants with Down's syndrome, particularly at the age of 12 months, and (2) cochlear function in infants with Down's syndrome may differ from normal infants by the age of 12 months.

Acoustic Stimulation↗
PubMed1980

Patterns of responses of cortical cells to binaural stimulation.

The relationship between stimulus intensity and response latency implies that the relative time of arrival of input to binaurally sensitive loci can vary over a range significantly longer than the interaural delays resulting from the travel time of sound between the ears. To investigate the effect of such potentially long inter-arrival time intervals, responses of binaurally sensitive neurons in auditory cortex of cats were examined over relatively long interaural delays. Two kinds of interaural delay functions were observed. One kind involved a sharp transition to a reduced response rate over a narrow range of interaural delays, while the other involved a gradual reduction of response rate over a relatively prolonged range of interaural delays. The amount of suppression was found to be a sensitive function of both interaural delay and the relative intensity of the stimuli delivered to the two ears. The pattern of suppression across a binaural response was stationary with respect to the excitatory contralateral stimulus over wide ranges of interaural delay. In addition, certain characteristics of a group of cells generally responsive only to binaural stimulation are described. A model is proposed which accounts for the observed stationarity of the response suppression.

Animals↗
PubMed1996

Habituation and sensitization of the acoustic startle response in rats: amplitude, threshold, and latency measures.

The amplitude of the acoustic startle response habituates to repetitive stimulation. The input and output of the startle system were measured to determine if the decrease in startle amplitude during repetitive stimulation is due to an increase in the startle threshold. Two experimental approaches were used in 35 Sprague-Dawley rats to probe the relationship between the input (the sound pressure level of the stimulus) and the behavioral output (startle amplitude). The results show that the minimum threshold for a response does not change during habituation; rather, the slope of the dependence of startle amplitude on stimulus level decreases. Because habituation does not influence startle threshold we propose that the site for habituation is located in the neural circuitry downstream from the site for startle threshold. Besides amplitude and threshold, as an additional parameter we measured startle latency. In general, the latency of the acoustic startle response is negatively correlated with the response amplitude. This correlation has been repeatedly shown, therefore one would expect a latency increase during the amplitude decrease caused by habituation. However, the latency of the startle reaction also decreased during the course of repetitive stimulation. According to the dual process theory of habituation, a stimulus has both a response-decreasing, i. e., habituating, as well as a response-increasing, i.e., sensitizing, influence on a behavior (Groves & Thompson, 1970). Our explanation of the present results is that startle amplitude is reduced following repetitive stimulation because it is mainly influenced by habituation; latency, however, is shortened because it is mainly influenced by sensitization.

Acoustic Stimulation↗
PubMed1985

Responses to pure tones and linear FM components of the CF-FM biosonar signal by single units in the inferior colliculus of the mustached bat.

The responses of 682 single-units in the inferior colliculus (IC) of 13 mustached bats (Pteronotus parnellii parnellii) were measured using pure tones (CF), frequency modulations (FM) and pairs of CF-FM signals mimicking the species' biosonar signal, which are stimuli known to be essential to the responses of CF/CF and FM-FM facilitation neurons in auditory cortex. Units were arbitrarily classified into 'reference frequency' (RF), 'FM2' and 'Non-echolocation' (NE) categories according to the relationship of their best frequencies (BF) to the biosonar signal frequencies. RF units have high Q10dB values and are tuned to the reference frequency of each bat, which ranged between 60.73 and 62.73 kHz. FM2 units had BF's between 50 and 60 kHz, while NE units had BF's outside the ranges of the RF and FM2 classes. PST histograms of the responses revealed discharge patterns such as 'onset', 'onset-bursting' (most common), 'on-off', 'tonic-on','pauser', and 'chopper'. Changes in discharge patterns usually resulted from changes in the frequency and/or intensity of the stimuli, most often involving a change from onset-bursting to on-off. Different patterns were also elicited by CF and FM stimuli. Frequency characteristics and thresholds to CF and FM stimuli were measured. RF neurons were very sharply tuned with Q10dB's ranging from 50-360. Most (92%) also responded to FM2 stimuli, but 78% were significantly more sensitive (greater than 5 dB) to CF stimuli, and only 3% had significantly lower thresholds to FM2. The best initial frequency for FM2 sweeps in RF units was 65.35 +/- 2.138 kHz (n = 118), well above the natural frequency of the 2nd harmonic. FM2 and NE units were indistinguishable from each other, but were quite different from RF units: 41% of these two classes had lower thresholds to CF, 49% were about equally sensitive, and 10% had lower thresholds to FM. For FM2 units, mean best initial frequency for FM was 60.94 kHz +/- 3.162 kHz (n = 114), which is closely matched to the 2nd harmonic in the biosonar signal. Very few units (5) responded only to FM signals, i.e., were FM-specialized. The characteristics of spike-count functions were determined in 587 units. The vast majority (79%) of RF units (n = 228) were nonmonotonic, and about 22% had upper-thresholds.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1980

Brain stem auditory evoked response development in the kitten.

The development of brain stem auditory evoked responses (BAERs), recorded from a surface electrode as short-latency, volume-conducted potentials, was studied in a series of kittens over a postnatal period ranging from birth to 60 days. Repeated, longitudinal observations on particular kittens were supplemented with observations on additional kittens during the first and second postnatal week to determine age of onset of the BAERs. The position of the animal and sound source within the recording chamber were held constant across recording sessions, as was click intensity except during recordings in which intensity effects were specifically studied. Click rates of 1, 10, 50 and 100/sec were routinely presented. Reference electrodes at the tongue, pinna and neck showed volume-conducted responses to the click stimuli and resulted in considerable distortion of the activity recorded by the vertex electrode; the forepaw, in contrast, showed no activity and a vertex-forepaw electrode configuration provided good resolution of the BAERs across development. A number of new observations were made. BAERs were first observed at 4 days of age, approximately the same age at which depth evoked potentials are first recorded in brain stem auditory nuclei. Initially the BAERs were diffuse, high threshold and fatigued rapidly, characteristics shared with depth evoked potentials in the early postnatal period. Over the first two weeks, the potentials showed marked decrease in threshold, increased resistance to fast click rates, and better definition of wave forms. All BAER components showed exponential decreases in latency. Because all of the brain stem evoked potentials could be recorded concurrently and longitudinally in the same subject a number of developmental comparisons were possible among the BAER components. Wave 1, related to the acoustic nerve in the adult cat, showed a developmental time course and adult latency similar to that reported for N1. Wave 2, related to the cochlear nucleus in the adult, showed a marked bimodality over the first month; wave 2a was a large amplitude clearly separated wave which gradually fused as an inconspicuous leading shoulder on wave 2b. Wave 2b developed with a time course and adult latency similar to that reported for the ventral cochlear nucleus. Wave 3, related to the region of the superior olivary complex in the adult, showed a clear but transient bimodality during the third week of development. Wave 5, related to the inferior colliculus in the adult, appeared later than waves 1-4 and showed a significantly slower rate of development than waves 1-4. These data indicate that differential developmental changes occur within the brain stem auditory pathway and that the BAERs provide a dynamic probe of concurrent maturational interactions.

Acoustic Stimulation↗
PubMed1985

The four factors leading to binaural masking-level differences.

A simple extension of the Webster-Jeffress model is presented together with its predictions for the effects of various stimulus parameters on the size of binaural masking-level differences (BMLDs). The four factors leading to BMLDs (just-noticeable differences (JNDs), temporal effects in simultaneous masking, binaural interaction, and temporal effects in non-simultaneous masking) are described, new measurements of the effect of signal duration on the detectability of interaural delay are presented, and the high degree of correlation between observers' sensitivity to changes in level and their sensitivity to changes in interaural delay is demonstrated. A number of examples illustrating where knowledge of JNDs for level and interaural delay and their joint dependence on certain stimulus parameters are sufficient to predict BMLDs are discussed.

Auditory Perception↗
PubMed1998

Right parietal cortex is involved in the perception of sound movement in humans.

Changes in the delay (phase) and amplitude of sound at the ears are cues for the analysis of sound movement. The detection of these cues depends on the convergence of the inputs to each ear, a process that first occurs in the brainstem. The conscious perception of these cues is likely to involve higher centers. Using novel stimuli that produce different perceptions of movement in the presence of identical phase and amplitude modulation components, we have demonstrated human brain areas that are active specifically during the perception of sound movement. Both functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) demonstrated the involvement of the right parietal cortex in sound movement perception with these stimuli.

Acoustic Stimulation↗