Age-related changes in auditory temporal processing.

Two tone bursts separated by a silent interval and imbedded in a background white noise were presented to elderly subjects (M age?=?71.3 years) and young subjects (M age?=?22.2 years). Subjects were required to judge when the two tone bursts fused perceptually by adjusting the duration of tone-one. The bursts were separated by six discrete interstimulus intervals of 4, 8, 16, 24, 32, or 40 ms. The tone-two burst was held constant at 100 ms. Fusion point was defined as that critical tone-one duration at which the two tones fused (were perceived as one). Elderly subjects reached fusion point at longer critical tone-one durations than young subjects at each interval tested. The function relating tone-one duration and interval conformed to an exponential curve and is discussed with respect to an exponential decay model of the inhibitory interactions of neural systems responding to onsets and offsets of sensory events. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The mismatch negativity to frequency deviant stimuli during natural sleep

Eight subjects spent a single night in the sleep laboratory. Event-related potentials (ERPs) were recorded during the presentation of two auditory "oddball' stimulus conditions in which tonal frequency was manipulated. In the first condition, 1000 Hz "standard' and 2000 Hz "deviant' tones were presented. In the second condition, the deviant tone was reduced to 1050 Hz. In both conditions, deviant probability was 0.2. Stimuli were presented every 600 ms during wakefulness and stages 2, 4, and REM of sleep. A distinctive N1 wave was visible in both stimulus conditions when the subject was awake. The deviant stimuli elicited a "mismatch negativity' (MMN) that inverted in polarity at the mastoid. In REM sleep, an N1 and a MMN were also elicited in both conditions. In the large deviance condition, the MMN had a slightly attenuated amplitude and was shorter in duration while in the small deviant condition, its peak latency was unusually early. Neither the N1 nor the MMN could be recorded in non-REM sleep.     

Reflex modification in the rat: The inhibitory effects of intensity and frequency changes in steady tones.

Four experiments with 50 male albino Charles River rats investigated the relation between the inhibitory effects of tonal frequency change and the length of the silent period (gap) preceding it. It is noted that, in both laboratory rats and in humans, a low-intensity tone that precedes a high-intensity burst of noise by approximately 100 msec can reduce the amplitude of the startle reaction elicited by the burst of noise. Overall results show that a gap in an otherwise continuous pure tone inhibited startle when the gap occurred approximately 100 msec prior to the noise burst. Although an increase in gap duration increased the inhibition afforded by the gap, the maximum inhibition was yielded by gaps of 100 msec and greater; this maximum was equivalent to the inhibition yielded by the presentation of a postgap tone alone. A shift in tonal frequency across a 10-msec gap yielded more inhibition than did the same gap with no frequency shift; again, the shift yielded equivalent inhibition to the presentation of the postgap tone alone. An increase in the frequency shift increased inhibition when the shift occurred across a 10-msec gap but not across a 100-msec gap. It is concluded that the amount of inhibition afforded by a complex acoustic event is more than a mere additive function of the inhibitory effects of the different elements that make up the event. For example, a tonal onset is just as inhibitory as a frequency shift across a gap, which includes a tonal onset, tonal offset, and frequency shift. (15 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The temporal window of two-tone facilitation in onset units of the ventral cochlear nucleus

Effects of a tone, not at the best frequency (BF), on the responses of onset units to BF tones were recorded in the ventral cochlear nucleus of the guinea pig. The off-BF tone was at a fixed non-excitatory sound level. When the two tones were gated simultaneously, a marked threshold facilitation was observed; however, no facilitation was observed if the off-BF tone burst was delayed by 5-10 ms. Facilitation in some units declined and was either absent or only just detectable, when the start of the off-BF tone preceded that of the BF by more than 10 ms. However, the responses of the majority of onset units were facilitated when the off-BF tone preceded the BF tone by as much as 20 ms. Similar results were obtained when the roles of the BF and off-BF tones were reversed. These data suggest that depolarization due to BF inputs is of shorter duration than that due to off-BF inputs.     

Mismatch negativity and auditory sensory memory evaluation: a new faster paradigm

A new faster paradigm to measure the duration of auditory sensory memory, as indexed by mismatch negativity (MMN) suppression to stimuli presented at increasing inter-stimulus intervals (ISI), is proposed. Trains of three stimuli were delivered at very short ISI (300 ms). The inter-train interval varied according to the memory probe interval (MPI) tested. Trains started randomly with a deviant or standard stimulus (50% each), with their event-related brain potentials subtracted to obtain the MMN. The new paradigm provided MMNs identical to the conventional one at MPIs of 0.4 and 4.0 s in young subjects, and revealed MMN suppression when the MPI was increased to 5.0 s in older subjects. The new paradigm estimates auditory sensory memory duration in one-third the time of conventional MMN.     

Detection of silent intervals between noises activating different perceptual channels: some properties of "central" auditory gap detection

This article describes four experiments on gap detection by normal listeners, with the general goal being to examine the consequences of using noises in different perceptual channels to delimit a silent temporal gap to be detected. In experiment 1, subjects were presented with pairs of narrow-band noise sequences. The leading element in each pair had a center frequency of 2 kHz and the trailing element's center frequency was parametrically varied. Gap detection thresholds became increasingly poor, sometimes by up to an order of magnitude, as the spectral disparity was increased between the noise bursts that marked the gap. These data suggested that gap-detection performance is impoverished when the underlying perceptual timing operation requires a comparison of activity in different perceptual channels rather than a discontinuity detection within a given channel. In experiment 2, we assessed the effect of leading-element duration in within-channel and between-channel gap detection tasks. Gap detection thresholds rose when the duration of the leading element was less than about 30 ms, but only in the between-channel case. In experiment 3, the gap-detection stimulus was redesigned so that we could probe the perceptual mechanisms that might be involved in stop consonant discrimination. The leading element was a wideband noise burst, and the trailing element was a 300-ms bandpassed noise centered on 1.0 kHz. The independent variable was the duration of the leading element, and the dependent variable was the smallest detectable gap between the elements. When the leading element was short in duration (5-10 ms), gap thresholds were close to 30 ms, which is close to the voice onset time that parses some voiced from unvoiced stop consonants. In experiment 4, the generality of the leading-element duration effect in between-channel gap detection was examined. Spectrally identical noises defining the leading and trailing edges of the gap were presented to the same or to different ears. There was a leading-element duration effect only for the between channel case. The mean gap threshold was again close to 30 ms for short leading-element durations. Taken together, the data suggest that gap detection requiring a temporal correlation of activity in different perceptual channels is a fundamentally different task to the discontinuity detection used to execute gap detection performance in the traditional, within-channel paradigm.     

Measurements of the temporal fMRI response of the human auditory cortex to trains of tones

Averaged single trials (AST) allowed the functional magnetic resonance imaging (fMRI) response to auditory stimuli to be measured at high temporal (1 s) and spatial (0.1 cm3) resolution. Using this paradigm we investigated the transient signal response to 100-ms tone bursts in trains of between 100 ms and 25.5 s in total duration. We have demonstrated that the fMRI response to such auditory stimuli is approximately linear for trains of 6 s and longer, but that shorter stimuli produce signals that are larger than might be expected from the response to the longer stimuli. This nonlinear behavior can be modeled if an adaptive response to each stimulus is assumed. A study using a novel paradigm was also performed in order to study the influence of scanner noise during fMRI experiments on the auditory system response to tones. This study demonstrated that the temporal response to 700-ms tone stimuli is modified when performed in the presence of scanner gradient noise, the modification being a small but significant increase (P < 0.05) in the magnitude of the response. Finally the ability to measure the onset of functional activation using the AST method was examined. It was found, with the aid of computer simulation that a sampling rate of one image per second is adequate to distinguish temporal responses. Using the data acquired in this study, onset times were calculated for the auditory cortex, and these results are consistent with current models of functional activation.     

Mismatch negativity: deviance detection or the maintenance of the 'standard'

Electric brain responses were measured to infrequent tones that broke the frequency alternation of two tones, deviated in duration or violated both regularities (alternation and constant duration). Mismatch negativity (MMN) was elicited by both simple deviants with the duration-related MMN peaking approximately 130 ms later than the alternation-related MMN. The double deviant elicited two successive MMNs. Thus violation of each regularity elicited a separate MMN, whereas previous studies showed that multiple temporally separate deviations from a single repetitive standard elicit one MMN only. These results suggest that the primary function of the MMN-generating process is more closely related to maintaining the representation of auditory regularities than to deviance detection per se.     

Pitch perception in chinchillas (Chinchilla laniger): Stimulus generalization using rippled noise.

Rippled noises evoke the perception of pitch in human listeners. Infinitely iterated rippled noise (IIRN) is generated when wideband noise (WBN) is delayed, attenuated, and added to the original WBN through either a positive (+) or a negative (-) feedback loop. The pitch of IIRN[+] is matched to the reciprocal of the delay, whereas the pitch of IIRN[-] for the same delay is an octave lower. Chinchillas (Chinchilla laniger) were trained to discriminate IIRN[+] with a 4-ms delay from IIRN[+] with a 2-ms delay and then tested in a stimulus generalization paradigm with IIRN[+] at delays between 2 and 4 ms. Systematic gradients in behavioral response occurred along the dimension of delay, suggesting that a perceptual dimension corresponding to pitch exists for IIRN[+]. Behavioral responses to IIRN[-] test stimuli were more variable among chinchillas, suggesting that IIRN[-] did not evoke similar pitches relative to IIRN[+]. Systematic gradients in behavioral response were observed when IIRN[-] test stimuli were presented in the context of other IIRN[-] stimuli. Thus, other perceptual cues such as timbre may dominate the pitch cues when IIRN[-] test stimuli are presented in the context of IIRN[+] stimuli. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Perceived lateral position of narrow-band noise in hearing-impaired and normal-hearing listeners under conditions of equal sensation level and sound-pressure level

The perceived lateral position of narrow-band noise (NBN) was studied in a graphic pointer task as a function of the method of compensation for interaural threshold asymmetries in hearing-impaired and normal-hearing subjects. The method of compensation consisted of equal sensation level (EqSL) or equal sound-pressure level (EqSPL) at the two ears within the same subject. The NBN signals were presented at 11 center frequencies with interaural intensity differences (IIDs) that varied from -20 to +20 dB. When equalizing by SL, the perceived lateral position is essentially linearly dependent on the degree and direction of asymmetry in asymmetric normal-hearing and hearing-impaired listeners. Equalizing by SPL shows no such dependency but produces images that are lateralized close to the midline. These results reveal that subjects may have adapted to their threshold asymmetries. These results will be discussed in terms of the fitting of binaural hearing aids.     

Features of ipsilaterally evoked inhibition in the dorsal nucleus of the lateral lemniscus

The dorsal nucleus of the lateral lemniscus (DNLL) is a binaural nucleus whose neurons are excited by stimulation of the contralateral ear and inhibited by stimulation of the ipsilateral ear. Here we report on several features of the ipsilaterally evoked inhibition in 95 DNLL neurons of the mustache bat. These features include its dependence on intensity, its tuning and the types of stimuli that are capable of evoking it. Inhibition was studied by evoking discharges with the iontophoretic application of glutamate, and then evaluating the strength and duration of the inhibition of the glutamate evoked background activity produced by stimulation of the ipsilateral ear. Excitatory responses were evoked by stimulation of the contralateral ear with best frequency (BF) tone bursts. Glutamate evoked discharges could be inhibited in all DNLL neurons and the inhibition often persisted for periods ranging from 10 to 50 ms beyond the duration of the tone burst that evoked it. The duration of the persistent inhibition increased with stimulus intensity. Stimulus duration had little influence on the duration of the persistent inhibition. Signals as short as 2 ms suppressed discharges for as long as 30 ms after the signal had ended. The frequency tuning of the total period of inhibition and the period of persistent inhibition were both closely matched to the tuning evoked by stimulation of the contralateral ear. Moreover, the effectiveness of complex signals for evoking persistent inhibition, such as brief FM sweeps and sinusoidally amplitude and frequency modulated signals, was comparable to that of tone bursts at the neuron's excitatory BF, so long as the complex signal contained frequencies at or around the neuron's excitatory BF. We also challenged DNLL cells with binaural paradigms. In one experiment, we presented a relatively long (40 ms) BF tone burst of fixed intensity to the contralateral ear, which evoked a sustained discharge, and a shorter, 10 ms signal of variable intensity to the ipsilateral ear. As the intensity of the 10 ms ipsilateral signal increased, it generated progressively longer periods of persistent inhibition and thus the discharges were suppressed for periods far longer than the 10 ms duration of the ipsilateral signal. With interaural time disparities, ipsilateral signals that led contralateral signals evoked a persistent inhibition that suppressed the responses to the trailing contralateral signals for periods of a least 15 ms. This suggests that an initial binaural sound that favors the ipsilateral ear should suppress the responses to trailing sounds that normally would be excitatory if they were presented alone. We hypothesize a circuit that generates the persistent inhibition and discuss how the results with binaural signals support that hypothesis.     

Inhibitory influences on asynchrony as a cue for auditory segregation.

A harmonic that begins before the other harmonics contributes less than they do to vowel quality. This reduction can be partly reversed by accompanying the leading portion with a captor tone. This effect is usually interpreted as reflecting perceptual grouping of the captor with the leading portion. Instead, it has recently been proposed that the captor effect depends on broadband inhibition within the central auditory system. A test of psychophysical predictions based on this proposal showed that captor efficacy is (a) maintained for noise-band captors, (b) absent when a captor accompanies a harmonic that continues after the vowel, and (c) maintained for 80 ms or more over a gap between captor offset and vowel onset. These findings support and refine the inhibitory account. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Spatial effects on tactile duration categorization.

The aim of this study was to measure the impact of the distance between tactile stimuli marking brief time intervals on perceived duration and threshold estimates. Each interval to be categorized as short or long (midvalue = 500 ms) was marked by two brief signals delivered on participants' left (L) or right (R) hand: L-L, R-R, L-R or R-L. The hands were placed nearby or at a distance of 3 feet (about 91 cm). Eight-point individual psychometric functions were drawn for each of the eight experimental conditions. The results reveal that when intervals are marked with signals delivered on different hands rather than on the same hand, they are perceived as longer. Moreover, no difference for perceived duration was observed between the L-L and R-R conditions, and between the L-R and R-L sequence. Finally, marking intervals with signals delivered at the same hand results in better temporal discrimination than with one signal delivered on each hand. The results with perceived duration are consistent with the kappa effect, but not with an attentional account of duration discrimination. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Activation of a distinct arousal state immediately after spontaneous awakening from sleep

In contrast to the many neural studies into the mechanisms of sleep onset and maintenance, few studies have focused specifically on awakening from sleep. However, the abrupt electrographic changes and large brief cardio-respiratory activation at awakening suggest that a distinct, transiently aroused, awake state may exist compared to later wakefulness. To test this hypothesis we utilized the acoustic startle reflex, a standard un-conditioned reflex elicited by a sudden loud noise. This reflex is modulated under specific conditions, one being a diminution of startle when a quieter pre-stimulus is presented immediately before the loud stimulus. This pre-pulse inhibition (PPI) is used as a measure of sensorimotor gating, with smaller PPI indicating less filtering of sensory inputs and increased responsiveness to external stimuli. Eight rats with electrodes for recording sleep-wake state were studied. An accelerometer measured startle responses. The startle reflex was elicited by 115 dB, 40 ms tones. PPI was produced by 74 dB, 20 ms tones preceding the 115 dB tone by 100 ms. Responses within 100 ms were measured. Stimuli were applied either 3-10 s after spontaneous awakenings, or in established wakefulness (> 30 s). Responses to the startle stimuli alone were similar in the different awake states (P = 0.821). However, PPI was smaller at awakening from non-REM sleep compared to established wakefulness (45.4 +/- 7.5% vs. 74.3 +/- 6.1%, P = 0.0002). PPI after awakening from REM sleep (52.8 +/- 17.9%) was not significantly different than established wakefulness (P = 0.297). Reduced PPI of the startle reflex at awakening from non-REM sleep supports the hypothesis that wakefulness immediately after spontaneous sleep episodes is neurophysiologically distinct from later wakefulness and associated with reduced gating of motor responses to sensory inputs. Spontaneous activation of this distinct, transiently aroused, state upon awakening may serve a protective function, preparing an animal to respond immediately to potentially threatening stimuli.     

Children's performance on pseudoword repetition depends on auditory trace quality: Evidence from event-related potentials.

This study explored the relation between phonological short-term memory and auditory-sensory processing in 7–9-year-old children. Twenty-four participants performed a pseudoword repetition test. The mismatch-negativity (MMN) component of auditory event-related brain potentials was obtained from 9 participants with the highest and 9 participants with the lowest scores on the test. The MMN indexes short-term auditory-sensory memory, including auditory-sensory representations for speech. It was recorded to just perceptible /baga/–/baka/ bisyllabic and easily discriminable 1000/1100-Hz tone contrasts with interstimulus intervals of 350 and 2,000 ms. The high and low repeaters differed significantly in MMN amplitude to speech stimuli at the shorter interstimulus interval. Thus, the accuracy of auditory-sensory processing seems to affect phonological short-term representations in school-age children and therefore may play a role in vocabulary development. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Memory prerequisites of mismatch negativity in the auditory event-related potential (ERP).

The mismatch negativity (MMN) is a component of the auditory event-related brain potential that occurs in response to infrequent changes in the physical properties of homogeneous series of sounds, even when Ss are instructed to ignore the auditory channel of stimulation. It has been proposed (e.g., R. N??t?nen, see record 1991-00298-001) that the MMN is generated by an automatic process in which a difference between the deviant sound and the previous, standard sound is detected by the brain. However, it is unclear how the form of memory involved is related to the rest of the memory system. The present study indicates that, for an MMN to be elicited in response to a change in tone frequency, the representation of the standard tone must be both well-established as a standard in memory and in a currently active state. The relation between physiological and psychological aspects of memory representation is discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Time perception in spatial neglect: A distorted representation?

Objective: It has been proposed that time, space, and numbers share the same metrics and cortical network, the right parietal cortex. Several recent investigations have demonstrated that the mental number line representation is distorted in neglect patients. The aim of this study is to investigate the relationship between time and spatial configuration in neglect patients. Method: Fourteen right-brain damaged patients (six with neglect and eight without neglect), as well as eight age-matched healthy controls, performed a time discrimination task. A standard tone (short: 700 ms and long: 1,700 ms) had to be confronted in duration to a test tone. Test tone differed of 100, 200, and 300 ms respect to the standard tone duration. Results: Neglect patients performed significantly worse than patients without neglect and healthy controls, irrespective of the duration of the standard tone. Conclusion: These results support the hypothesis that mental representations of space and time both share, to some extent, a common cortical network. Besides, spatial neglect seems to distort the time representation, inducing an overestimation of time durations. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Auditory frequency discrimination in the white rat

Frequency discrimination was investigated in the albino rat using a modified go/no-go positive reinforcement procedure in which subjects reported frequency increments in an ongoing series of pure tone bursts. Weber ratios (frequency difference limen/frequency) were measured from 5 to 32 kHz at 50 dB sound pressure level. A signal detection analysis of the procedure enabled a direct comparison to be made with the rat's performance in a discrete trial go/no-go task. A mean Weber ratio of 3.06+/-0.44% was measured in the frequency range 5-32 kHz. This indicates that the rat has better frequency discrimination acuity than has previously been thought. The result is discussed in the context of factors affecting performance. Among the factors that were explored we found that long training times and the specific training paradigm played important roles. In comparison to discrete trial go/no-go paradigms, rats performed much better when detecting signals from a repeating background. Frequency discrimination performance decreased linearly for tones less than 50 ms in duration. For longer tone duration performance was unaffected. The means and variability of reaction times for threshold changes of frequency were greater in comparison with supra-threshold frequency changes.     

Effects of varying signal duration on pure-tone frequency discrimination in humans and monkeys

This study examined the effects of varying signal duration and pulse repetition rate on pure tone frequency difference limens (FDLs) at 500 Hz and 4 kHz in humans and monkeys. Two experiments examined FDLs as a function of tone duration from 12-400 ms, using stimuli presented either with a constant pulse rate, or with a constant interstimulus interval. In both cases, at 500 Hz, human FDLs increased more than monkey FDLs as duration decreased from 400 to 12 ms. This effect resulted in monkey FDLs that were about 14 times larger than human FDLs at 400 ms, but only about 4 times larger at 12 ms. At 4 kHz, human and monkey FDLs showed more similar rates of increase as duration decreased. A third experiment examined FDLs at 500 Hz for a 100-ms tone as a function of pulse rate (1 per 250-2000 ms). Here, FDLs for humans and monkeys varied in a similar fashion, indicating that both species' sensitivity was similarly affected by manipulating temporal variables relating to memory load, rather than sensory coding. These data provide evidence that, at 500 Hz, humans have a qualitatively different pure tone frequency analyzing mechanism from monkeys, possibly based on better access to phase-locking mechanisms.     

Sensitivity of the mouse to changes in azimuthal sound location: Angular separation, spectral composition, and sound level.

Auditory spatial acuity was measured in mice using prepulse inhibition (PPI) of the acoustic startle reflex as the indicator response for stimulus detection. The prepulse was a “speaker swap” (SSwap), shifting a noise between two speakers located along the azimuth. Their angular separation, and the spectral composition and sound level of the noise were varied, as was the interstimulus interval (ISI) between SSwap and acoustic startle reflex elicitation. In Experiment 1 a 180° SSwap of wide band noise (WBN) was compared with WBN Onset and Offset. SSwap and WBN Onset had near equal effects, but less than Offset. In Experiment 2 WBN SSwap was measured with speaker separations of 15, 22.5, 45, and 90°. Asymptotic level and the growth rate of PPI increased with increased separation from 15 to 90°, but even the 15° SSwap provided significant PPI for the mean performance of the group. SSwap in Experiment 3 used octave band noise (2–4, 4–8, 8–16, or 16–32 kHz) and separations of 7.5 to 180°. SSwap was most effective for the highest frequencies, with no significant PPI for SSwap below 8–16 kHz, or for separations of 7.5°. In Experiment 4 SSwap had WBN sound levels from 40 to 78 dB SPL, and separations of 22.5, 45, 90, and 180°: PPI increased with level, this effect varying with ISI and angular separation. These experiments extend the prior findings on sound localization in mice, and the dependence of PPI on ISI adds a reaction time-like dimension to this behavioral analysis. (PsycINFO Database Record (c) 2010 APA, all rights reserved)