PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Auditory Perception”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 595 records · Page 33Linked to original sources

Multisensory integration of speech signals: the relationship between space and time.

Integrating audiovisual cues for simple events is affected when sources are separated in space and time. By contrast, audiovisual perception of speech appears resilient when either spatial or temporal disparities exist. We investigated whether speech perception is sensitive to the combination of spatial and temporal inconsistencies. Participants heard the bisyllable /aba/ while seeing a face produce the incongruent bisyllable /ava/. We tested the level of visual influence over auditory perception when the sound was asynchronous with respect to facial motion (from -360 to +360 ms) and emanated from five locations equidistant to the participant. Although an interaction was observed, it was not related to participants' perception of synchrony, nor did it indicate a linear relationship between the effect of spatial and temporal discrepancies. We conclude that either the complexity of the signal or the nature of the task reduces reliance on spatial and temporal contiguity for audiovisual speech perception.

Acoustic Stimulation↗

Functional zones in the auditory cortex of the echolocating bat, Myotis lucifugus.

Neurophysiological mapping experiments in the auditory cortex of the frequency-modulated bat, Myotis lucifugus, reveal 3 functional subregions: a tonotopic zone located dorsally, a delay-sensitive zone more ventrally, and an intermediate zone of major overlap. The unique finding of an overlapping cortical region representing both spectral and time-delay information of echoes is intriguing in view of a recent behavioral study suggesting the convergence of such echo cues in auditory perception. (Simmons et al., Soc. Neurosci. Abstr., 13 [1987] 870).

Acoustic Stimulation↗

2-Deoxyglucose uptake patterns in response to pure tone stimuli in the aged rat inferior colliculus.

The tonotopic map of the inferior colliculus (IC) of aged rats (25 months old) was examined to determine whether age-related changes known to occur in the cochlea are reflected in the 2-deoxyglucose (2-DG) uptake pattern of the IC. Because aged animals have hearing losses, auditory brainstem response thresholds were measured. Animals with threshold shifts of no greater than 30 dB relative to young animals were used. Animals were injected with radiolabeled 2-DG and stimulated with continuous pure tones presented at 70 dB above the behavioral thresholds for young animals at either 1, 4 or 32 kHz for one hour in a sound attenuated booth. The stimulus sound pressure levels were chosen to achieve comparable sensation levels between the young and aged animals. The tonotopic map of the IC in aged rats was different from that reported previously for young animals (Ryan et al., 1988), in that, the regions stimulated by 1 and 4 kHz were shifted towards the higher frequencies and the uptake areas were twice as broad for the aged animals as for the young animals. The observed 2-DG uptake patterns are consistent with an activation pattern of a high intensity stimulus and a loss of responsive elements in the cochlear apex. Similar broad and shifted bands of activated tissue may contribute to difficulties in auditory perception in aged humans with increased thresholds and sound amplification.

Acoustic Stimulation↗

Attentional modulation of human auditory cortex.

Attention powerfully influences auditory perception, but little is understood about the mechanisms whereby attention sharpens responses to unattended sounds. We used high-resolution surface mapping techniques (using functional magnetic resonance imaging, fMRI) to examine activity in human auditory cortex during an intermodal selective attention task. Stimulus-dependent activations (SDAs), evoked by unattended sounds during demanding visual tasks, were maximal over mesial auditory cortex. They were tuned to sound frequency and location, and showed rapid adaptation to repeated sounds. Attention-related modulations (ARMs) were isolated as response enhancements that occurred when subjects performed pitch-discrimination tasks. In contrast to SDAs, ARMs were localized to lateral auditory cortex, showed broad frequency and location tuning, and increased in amplitude with sound repetition. The results suggest a functional dichotomy of auditory cortical fields: stimulus-determined mesial fields that faithfully transmit acoustic information, and attentionally labile lateral fields that analyze acoustic features of behaviorally relevant sounds.

Acoustic Stimulation↗

Modality specific neural correlates of auditory and somatic hallucinations.

Somatic hallucinations occur in schizophrenia and other psychotic disorders, although auditory hallucinations are more common. Although the neural correlates of auditory hallucinations have been described in several neuroimaging studies, little is known of the pathophysiology of somatic hallucinations. Functional magnetic resonance imaging (fMRI) was used to compare the distribution of brain activity during somatic and auditory verbal hallucinations, occurring at different times in a 36 year old man with schizophrenia. Somatic hallucinations were associated with activation in the primary somatosensory and posterior parietal cortex, areas that normally mediate tactile perception. Auditory hallucinations were associated with activation in the middle and superior temporal cortex, areas involved in processing external speech. Hallucinations in a given modality seem to involve areas that normally process sensory information in that modality.

Adult↗

Nonprimary auditory thalamic representation of acoustic change.

1. The mismatch response, or mismatch negativity (MMN), is a neurophysiologic response to stimulus change. In humans and other animals, the MMN may underlie the ability to discriminate acoustic differences, a fundamental aspect of auditory perception. 2. This study investigated the role of the thalamus in the generation of a tone-evoked MMN in guinea pigs. Electrodes were placed in the caudomedial (nonprimary) and ventral (primary) subdivisions of the auditory thalamus (medial geniculate nucleus). Surface epidural electrodes were placed at the midline and over the temporal lobe. The MMN was elicited by a deviant stimulus (2,450-Hz tone burst) embedded in a sequence of standard stimuli (2,300-Hz tone bursts). 3. A tone-evoked MMN was present in nonprimary thalamus but was absent in the primary thalamus. Surface-recorded MMNs were measured at the midline but not over the temporal lobe. The correspondence between nonprimary thalamic responses and midline surface potentials, and between primary thalamic responses and temporal surface potentials, is consistent with data reported for the auditory middle latency responses in guinea pigs. 4. The results demonstrate that the nonprimary auditory thalamus contributes to the generation of a tone-evoked MMN in the guinea pig. Furthermore, the data indicate that the guinea pig is a feasible model for investigating central auditory processes underlying acoustic discrimination.

Acoustic Stimulation↗

Auditory perceptual consolidation in early-onset blindness.

Early-onset blindness (EB) produces measurable advantages in auditory perception, attention, memory and language. Neville and Bavelier [Neville, H. J., & Bavelier, D. (2001) Variability of developmental plasticity. In J. L. McClelland, R. S. Siegler (Eds.) Mechanisms of cognitive development: Behavioral andellon symposia on cognition (pp. 271-301)] hypothesized that faster temporal processing underlies many auditory compensatory effects in the blind. We tested this hypothesis by comparing early-onset blind individuals and sighted counterparts (SC) by assessing their rates of perceptual consolidation, the accurate perceptual representation of auditory stimuli. Firstly, we first tested both groups on a temporal-order judgment task (TOJ). EB subjects had significantly lower TOJ thresholds than the SC subjects. Secondly, we assessed perceptual consolidation speed using auditory backward masking tasks, taking into account individual TOJ thresholds. Discrimination performance was unaffected at all mask delays in the EB group while the SC subjects needed a mask delay of 160 ms to perform comparably. A backward masking task using single tone stimuli found no differences between the EB and SC groups any mask delay. A simultaneous masking task demonstrated that the mask effectively impaired discrimination in EB subjects at sensory stages. These results suggest that advantages in perceptual consolidation may reflect a mechanism responsible for the short response times and better performance reported in early blind individuals across a number of complex auditory tasks.

Adaptation, Physiological↗

Auditory problems in elderly patients with stroke.

Twenty-five CAT-scan-confirmed stroke patients and 25 matched controls were studied. All the stroke patients were stable 2-3 months after unilateral hemispheric stroke. Those with ear disease, other central neurological disorder, severe dysphasia and acute or chronic confusion were excluded. There were no significant differences between the groups for average pure tone hearing threshold (APTT) or ability to discriminate pre-recorded speech presented to one ear at 35 decibels (dB) above APTT. The stroke subjects had significantly impaired performance on dichotic competing sentence testing (DCST). Seventeen stroke patients but only one control subject failed DCST. Failure rate was similar for left and right stroke and for temporal and non-temporal lobe involvement. Two-thirds of patients failing DCST did so in the ear opposite the side of the cortical lesion. We conclude that (i) DCST is useful in detecting central auditory dysfunction in stroke patients; and (ii) stroke can affect central auditory perception in older patients.

Aged↗

Cochlear implantation in children under the age of two: the MHH experience with the CLARION cochlear implant. Medizinische Hochschule Hannover.

This paper examines reports on the selection criteria, the surgical procedure, and the postoperative performance for children under the age of 2 implanted with the CLARION Multi-Strategy Cochlear Implant (1.2 device). Eighteen children have been implanted since 1996 with a mean age at implantation of 18 months (range 11 to 23 months). All children were selected by means of a standardized preoperative diagnostic protocol. The surgical procedure used in older children was modified depending on the head and mastoid size, skull thickness, and recurrent otitis media. Auditory perception was tested prior to as well as 3, 6, 12, and 18 months following implantation by means of a standardized age-adapted test protocol. The electrode array was inserted without difficulty in all cases, with no complications to date. On average, auditory performance improved over time up to 18 months after implantation. Closed-set test scores increased by 25% to 55% in 18 months. Open-set test scores began to show improvement between 6 and 12 months postoperatively. Overall, our experience indicates that cochlear implantation in children under the age of 2 is relatively safe and reliable. The Clarion 1.2 device surgery can be performed without complications. Auditory performance results support the effectiveness of early implantation.

Cochlear Implantation↗

Artificial implementation of auditory neurons: a comparison of biologically motivated models and a new transfer function oriented model.

Auditory perception neurons, also called inner hair cells (IHCs) because of their physical shape, transform the mechanical movements of the basilar membrane into electrical impulses. The impulse coding of the IHC is the main information carrier in the auditory process and is the basis for improvements in cochlear implants as well as for low-rate, high-quality speech processing and compression. This paper compares biologically motivated models (Meddis, Cooke, Payton) with a newly developed model which is transfer function oriented. The new model has only three reservoirs and the parameters can be controlled through five small ROM tables. This model is compared with the often used Meddis model in terms of accuracy, system parameter flexibility, and hardware effort in an FPGA implementation.

Auditory Pathways↗

Thresholds of discomfort for complex stimuli: acoustic and sound-quality predictors.

The purpose of this study was to explain differences in threshold of discomfort (TD) across complex stimuli using acoustic and sound-quality variables as predictors. Two 4-tone complexes and 10 environmental sounds were used as stimuli. The environmental sounds consisted of a baby crying, hairdryer blowing, glass breaking, jet engine propelling, person laughing, motorcycle accelerating, orchestra tuning, telephone ringing, siren blowing, and toilet flushing. One-third octave band (1/3 OB) spectra were obtained for the 12 stimuli, with overall rms amplitude held constant across the stimuli. Nine acoustic quantities describing the high- and low-frequency content, peakiness, and bandwidth of each 1/3 OB spectrum were defined. Twenty adult subjects, 6 men and 14 women, with normal hearing sensitivity participated in the study. TDs were obtained from each subject for all of the stimuli. In addition, subjects rated each of the stimuli for annoyance, harshness, loudness, noisiness, and tinniness on a 10-point scale. These ratings were completed at a level 10 dB below each subjects TD for that stimulus. A hierarchical multiple regression analysis was used to estimate the amount of variance in TDs accounted for by subject differences, defined acoustic properties, and sound-quality ratings. Results indicated that, after controlling for intersubject differences, acoustic and sound-quality factors significantly influenced TD ratings. Increases in high-frequency cutoff and low-frequency cutoff, as well as higher ratings of loudness and annoyance, were associated with higher TDs. Associated with lower TDs were an increase in the frequency of the primary spectral peak, an increase in the number of spectral peaks, an increase in the center frequency, an increase in the area under the frequency response curve 30 dB down from the peak amplitude, an increase in the calculated loudness level re ANSI S3.4-1980, and higher ratings of tinniness.

Acoustics↗

Asymmetry of masking between noise and iterated rippled noise: evidence for time-interval processing in the auditory system.

This study describes the masking asymmetry between noise and iterated rippled noise (IRN) as a function of spectral region and the IRN delay. Masking asymmetry refers to the fact that noise masks IRN much more effectively than IRN masks noise, even when the stimuli occupy the same spectral region. Detection thresholds for IRN masked by noise and for noise masked by IRN were measured with an adaptive two-alternative, forced choice (2AFC) procedure with signal level as the adaptive parameter. Masker level was randomly varied within a 10-dB range in order to reduce the salience of loudness as a cue for detection. The stimuli were filtered into frequency bands, 2.2-kHz wide, with lower cutoff frequencies ranging from 0.8 to 6.4 kHz. IRN was generated with 16 iterations and with varying delays. The reciprocal of the delay was 16, 32, 64, or 128 Hz. When the reciprocal of the IRN delay was within the pitch range, i.e., above 30 Hz, there was a substantial masking asymmetry between IRN and noise for all filter cutoff frequencies; threshold for IRN masked by noise was about 10 dB larger than threshold for noise masked by IRN. For the 16-Hz IRN, the masking asymmetry decreased progressively with increasing filter cutoff frequency, from about 9 dB for the lowest cutoff frequency to less than 1 dB for the highest cutoff frequency. This suggests that masking asymmetry may be determined by different cues for delays within and below the pitch range. The fact that masking asymmetry exists for conditions that combine very long IRN delays with very high filter cutoff frequencies means that it is unlikely that models based on the excitation patterns of the stimuli would be successful in explaining the threshold data. A range of time-domain models of auditory processing that focus on the time intervals in phase-locked neural activity patterns is reviewed. Most of these models were successful in accounting for the basic masking asymmetry between IRN and noise for conditions within the pitch range, and one of the models produced an exceptionally good fit to the data.

Adult↗

Gap detection as a function of frequency, bandwidth, and level.

The threshold for detection of a temporal gap in a noiseband was measured. A notched noise masker was used to restrict listening to a limited spectral region. Threshold was measured as a function of center frequency, bandwidth, and level. For a signal bandwidth of one-half the center frequency, the gap threshold decreased from 22.5 ms for a center frequency of 0.2 kHz to 3.2 ms at 8.0 kHz: a wideband condition provided an estimate of 2.3 ms, a value in agreement with previously published estimates. Bandwidth manipulation showed that the variation with frequency was not due to changes in absolute bandwidth alone. The effect of changes in level was determined at three frequencies, 0.4, 1.0, and 6.5 kHz, using a signal bandwidth of half the center frequency. At all frequencies gap threshold decreased as the signal spectrum level was raised from 10 to 25 dB, but a further increase to 40 dB showed no additional improvement. At frequencies up to about 1.0 kHz, the variation of gap threshold with frequency matches well the reciprocal of the bandwidth of the auditory filter, as determined from masking experiments using a notched-noise masker. This suggests that the temporal response of the auditory filter may limit gap detection at low frequencies.

Auditory Perception↗

Distribution of auditory-filter bandwidths at 2 kHz in young normal listeners.

Auditory-filter shapes at 2 kHz were estimated for 95 young normally hearing subjects using a notched-noise masker with spectrum level of 45 dB. Excluding two subjects with a recent history of noise exposure, the equivalent rectangular bandwidths (ERBs) of the filters were approximately normally distributed but the distribution had a slight positive skew. The mean ERB was 308 Hz and the standard deviation was 32 Hz. The two noise-exposed subjects had ERBs of 404 and 497 Hz.

Acoustic Stimulation↗