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At least 595 records · Page 33Linked to original sources
PubMed2002

Representation of phonological categories: a functional role for auditory columns.

A speculative model for representing phonological categories for stop place of articulation is offered. The model is analogous to neural columns in both inferotemporal cortex in the macaque for achieving constancy in object recognition and in the inferior colliculus of the barn owl for resolving ambiguous phase disparities for sound localization. Hypothetical auditory columns for encoding the vowel context-induced variability of F2 transitions are described using acoustic data from locus equation scatterplots of human speech. Such analyses serve to absorb the allophonic variability inherent in coarticulated speech utterances.

Animals↗
PubMedDate not supplied

Neural plasticity in processing of sound location by the early blind: an event-related potential study.

Event-related potentials (ERPs) to a change in the locus of origin of a repetitive sound were studied in early blind human subjects. It was found that the N2b component of the ERP was posteriorly distributed on the scalp to that in the sighted control subjects. This suggests that the blind might use, to a larger extent than the sighted, parietal, or perhaps even occipital, brain areas in sound localization. The present results thus appear to demonstrate plastic changes in neural populations involved in processing of auditory space following early loss of vision.

Acoustic Stimulation↗
PubMed1994

Hearing in prairie dogs: transition between surface and subterranean rodents.

Behavioral audiograms were determined for four black-tailed and one white-tailed prairie dogs (Cynomys ludovicianus and C. leucurus) using a conditioned avoidance procedure. The hearing of black-tailed prairie dogs ranges from 29 Hz to 26 kHz and that of the white-tailed prairie dog from 44 Hz to 26 kHz (at sound pressure levels of 60 dB). Both species have good low-frequency hearing, especially black-tailed prairie dogs which can hear as low as 4 Hz and are more sensitive than any other rodent yet tested at frequencies below 63 Hz. In contrast, prairie dogs are relatively insensitive in their midrange and have poor high-frequency hearing. It is suggested that the reduced midrange sensitivity and high-frequency hearing are related to their adaptation to an underground lifestyle with its reduced selective pressure for sound localization. In this respect they appear to be intermediate between the more exclusively subterranean rodents (such as gophers and mole rats) and surface dwellers (such as chinchillas and kangaroo rats).

Acoustic Stimulation↗
PubMed2001

Systematic distortions of auditory space perception following prolonged exposure to broadband noise.

Perceptual distortions referred to as aftereffects may arise following exposure to an adapting sensory stimulus. The study of aftereffects has a long and distinguished history [Kohler and Wallach, Proc. Am. Philos. Soc. 88, 269-359 (1944)] and a range of aftereffects have been well described in sensory modalities such as the visual system [Barlow, in Vision: Coding and Efficiency (Cambridge University Press, Cambridge, 1990)]. In the visual system these effects have been interpreted as evidence for a population of cells or channels specific for certain features of a stimulus. However there has been relatively little work examining auditory aftereffects, particularly in respect of spatial location. In this study we have examined the effects of a stationary adapting noise stimulus on the subsequent auditory localization in the vicinity of the adapting stimulus. All human subjects in this study were trained to localize short bursts of noise in a darkened anechoic environment. Adaptation was achieved by presenting 4 min of continuous noise at the start of each block of trials and was maintained by a further 15-s noise burst between each trial. The adapting stimulus was located either directly in front of the subject or 30 degrees to the right of the midline. Subjects were required to determine the location of noise burst stimuli (150 ms) in the proximity of the adapting stimulus following each interstimulus period of adaptation. Results demonstrated that following adaptation there was a general radial displacement of perceived sound sources away from the location of the adapting stimulus. These data are more consistent with a channel-based or place-based process of sound localization rather than a simple level-based adaptation model. A simple "distribution shift" model that assumes an array of overlapping spatial channels is advanced to explain the psychophysical data.

Adult↗
PubMed2003

Likelihood approaches to sensory coding in auditory cortex.

Likelihood methods began their evolution in the early 1920s with R A Fisher, and have developed into a rich framework for inferential statistics. This framework offers tools for the analysis of the differential geometry of the full likelihood function based on observed data. We examine likelihood functions derived from inverse Gaussian (IG) probability density models of cortical ensemble responses of single units. Specifically, we investigate the problem of sound localization from the observation of an ensemble of neural responses recorded from the primary (Al) field of the auditory cortex. The problem is framed as a probabilistic inverse problem with multiple sources of ambiguity. Observed and expected Fisher information are defined for the IG cortical ensemble likelihood functions. Receptive field functions of multiple acoustic parameters are constructed and linked to the IG density. The impact of estimating multiple acoustic parameters related to the direction of a sound is discussed, and the implications of eliminating nuisance parameters are considered. We examine the degree of acuity afforded by a small ensemble of cortical neurons for locating sounds in space, and show the predicted patterns of estimation errors, which tend to follow psychophysical performance.

Acoustic Stimulation↗
PubMed2003

Auditory localization in the horizontal plane with single and double hearing protection.

INTRODUCTION: Although single hearing protection devices such as earplugs or earmuffs are known to degrade sound localization, little is known about localization accuracy in double-hearing-protection conditions where both earplugs and earmuffs are worn at the same time. METHODS: Listeners wearing earplugs, earmuffs, or a combination of earplugs and earmuffs were asked to localize short (250 ms) or long (continuous) pink noise signals originating from one of 24 loudspeaker locations in the horizontal plane. RESULTS: When single hearing protection was worn, localization was reasonably accurate in the left-right dimension even when the stimuli were short in duration. When double hearing protection was worn, however, left-right localization accuracy was poor even when the stimuli were on continuously. A second experiment showed that localization accuracy with double hearing protection varied substantially across different listeners, but that it varied only slightly across refittings of the same earplugs and earmuffs on the same listener. A third experiment showed that double hearing protection impaired localization in the left-right dimension much more for narrow-band sounds at frequencies above 500 Hz than it did for narrowband sounds at frequencies at or below 250 Hz. DISCUSSION: The severe disruptions in performance that occurred when earmuffs and earplugs were worn simultaneously suggest the influence of a mechanism such as bone conduction that does not normally interfere with localization when only a single hearing protection device is used.

Adult↗
PubMed2000

Effects of inhibitory timing on contrast enhancement in auditory circuits in crickets (Teleogryllus oceanicus).

In crickets (Teleogryllus oceanicus), the paired auditory interneuron Omega Neuron 1 (ON1) responds to sounds with frequencies in the range from 3 to 40 kHz. The neuron is tuned to frequencies similar to that of conspecific songs (4.5 kHz), but its latency is longest for these same frequencies by a margin of 5-10 ms. Each ON1 is strongly excited by input from the ipsilateral ear and inhibits contralateral auditory neurons that are excited by the contralateral ear, including the interneurons ascending neurons 1 and 2 (AN1 and AN2). We investigated the functional consequences of ON1's long latency to cricket-like sound and the resulting delay in inhibition of AN1 and AN2. Using dichotic stimuli, we controlled the timing of contralateral inhibition of the ANs relative to their excitation by ipsilateral stimuli. Advancing the stimulus to the ear driving ON1 relative to that driving the ANs "subtracted" ON1's additional latency to 4.5 kHz. This had little effect on the spike counts of AN1 and AN2. The response latencies of these neurons, however, increased markedly. This is because in the absence of a delay in ON1's response, inhibition arrived at AN1 and AN2 early enough to abolish the first spikes in their responses. This also increased the variability of AN1 latency. This suggests that one possible function of the delay in ON1's response may be to protect the precise timing of the onset of response in the contralateral AN1, thus preserving interaural difference in response latency as a reliable potential cue for sound localization. Hyperpolarizing ON1 removed all detectable contralateral inhibition of AN1 and AN2, suggesting that ON1 is the main, if not the only, source of contralateral inhibition.

Acoustic Stimulation↗
PubMed2002

Functional architecture of auditory cortex.

Three complementary approaches demonstrate new types of organization in rodent, feline and primate auditory cortex, as well as differences in processing between auditory and visual cortex. First, connectional work reveals patterns of thalamocortical and corticocortical input unique to the auditory cortex. Second, physiological studies find multiple, interleaved auditory processing modules related to corticocortical connections and embedded in the isofrequency gradient. Third, functional analyses demonstrate independent processing streams for sound localization and identification analogous to the 'what' and 'where' streams in visual cortex, although the modular arrangements are modality-specific. Taken together, these data show that the auditory cortex has common and unique functional substrates.

Animals↗
PubMed1986

Auditory performance of children with unilateral sensorineural hearing loss.

Horizontal sound localization and syllable recognition skills were examined in a group of children with unilateral sensorineural hearing loss and a matched group of normal hearers. The results showed that the unilaterally hearing-impaired children performed more poorly than the normal counterparts in both localization and speech recognition of nonsense syllables. The unilaterally hearing-impaired children had considerable difficulty understanding in a background of noise. The clinical implications of these findings are discussed.

Achievement↗
PubMed1997

Audiogram of the big brown bat (Eptesicus fuscus).

The audiograms of three big brown bats (Eptesicus fuscus) were determined using a conditioned avoidance procedure. The average audiogram ranged from 0.850 kHz at 106 dB to 120 kHz at 83 dB SPL, with a best threshold of 7 dB at 20 kHz and a distinct decrease in sensitivity at 45 kHz. The results confirm those of a previous study by Dalland (1965a) that the big brown bat has good high-frequency hearing coupled with poor low-frequency hearing. Comparative analysis suggests that the bat's good high-frequency hearing initially evolved for passive sound localization and that it was later coopted for use in echolocation. In addition, the restricted low-frequency hearing of the big brown bat is typical of mammals with good high-frequency hearing.

Acoustic Stimulation↗
PubMed2005

Localization of aerial pure tones by pinnipeds.

In this study, minimum audible angles (MAAs) of aerial pure tones were measured in and compared between a northern elephant seal (Mirounga angustirostris), a harbor seal (Phoca vitulina), and a California sea lion (Zalophus californianus). Testing was conducted between 0.8 and 16 kHz in the elephant seal and 0.8 and 20 kHz in the harbor seal and sea lion in a hemi-anechoic chamber using a left/right psychophysical procedure. Performance for the same frequencies was also quantified for discrete speaker separation of 5 degrees from the mid-line. For all subjects, MAAs ranged from approximately 3 degrees to 15 degrees and were generally equal to or larger than those previously measured in the same subjects with a broadband signal. Performance at 5 degrees ranged from chance to 97% correct, depending on frequency and subject. Poorest performance in the sea lion and harbor seal occurred at intermediate frequencies, which is consistent with the duplex theory of sound localization. In contrast, the elephant seal's poorest performance occurred at higher frequencies. The elephant seal's result suggests an inferior ability to utilize interaural level differences and is perhaps related to best hearing sensitivity shifted toward lower frequencies in this species relative to other pinnipeds.

Acoustics↗
PubMed2000

A systematic representation of interaural intensity differences in the auditory cortex of the pallid bat.

The current model of cortical processing of auditory spatial information is based on an orthogonal representation of frequency and binaural response properties, but how this arrangement leads to representation of space in the auditory cortex is unclear. This study describes the first evidence of a cortical substrate for the systematic representation of space in a region of primary auditory cortex of the pallid bat that subserves passive sound localization. The organizational feature of this region is a systematic shift in sensitivity to interaural intensity differences across the cortical surface, suggesting a topographic representation of horizontal space based on the distribution of activity within the neuron population.

Animals↗
PubMed2001

Effects of binaural decorrelation on neural and behavioral processing of interaural level differences in the barn owl (Tyto alba).

The effect of binaural decorrelation on the processing of interaural level difference cues in the barn owl (Tyto alba) was examined behaviorally and electrophysiologically. The electrophysiology experiment measured the effect of variations in binaural correlation on the first stage of interaural level difference encoding in the central nervous system. The responses of single neurons in the posterior part of the ventral nucleus of the lateral lemniscus were recorded to stimulation with binaurally correlated and binaurally uncorrelated noise. No significant differences in interaural level difference sensitivity were found between conditions. Neurons in the posterior part of the ventral nucleus of the lateral lemniscus encode the interaural level difference of binaurally correlated and binaurally uncorrelated noise with equal accuracy and precision. This nucleus therefore supplies higher auditory centers with an undegraded interaural level difference signal for sound stimuli that lack a coherent interaural time difference. The behavioral experiment measured auditory saccades in response to interaural level differences presented in binaurally correlated and binaurally uncorrelated noise. The precision and accuracy of sound localization based on interaural level difference was reduced but not eliminated for binaurally uncorrelated signals. The observation that barn owls continue to vary auditory saccades with the interaural level difference of binaurally uncorrelated stimuli suggests that neurons that drive head saccades can be activated by incomplete auditory spatial information.

Animals↗
PubMed1992

Changing-loudness aftereffect following simulated movement: implications for channel hypotheses concerning sound level change and movement.

Listening to a tone changing unidirectionally in sound level causes an illusion of changing loudness in a steady tone afterward. This aftereffect may indicate channels for detecting the feature of change in sound level, which would primarily concern dynamic sound localization. Three subjects, one of whom was the author, participated in this study. The author predicted that opposite adaptation of the ears (the adapting stimulus is heard to move from one ear to the other) should lead to a movement aftereffect. This was not reported by the subjects. However, the subjects did report a changing-loudness aftereffect in a monaural test stimulus, and the characteristics of the changing-loudness aftereffect (such as its magnitude) were consistent with previous data, suggesting a two-stage channel hypothesis: Output from channels for several features, including sound-level change, simultaneously stimulate movement channels.

Attention↗
PubMed2000

Coding for auditory space in the superior colliculus of the rat.

Although the rat is often used to determine behavioural sound-localization capabilities or neuronal computation of binaural information, the representation of auditory space in the rat brain has not been investigated so far. We obtained extracellular recordings from auditory neurons in the superior colliculus of anaesthetized rats and examined them for spatial tuning characteristics and topographical order. Many neurons (73%) showed significant tuning, with a single peak in the azimuth response profiles based on spike rates and response latencies. Best azimuth values from neurons in one SC were generally tuned to contralateral and rarely to frontal or ipsilateral directions. Tuning width was mostly broad; at supra-threshold sound pressure levels (35 dB SPL), 55% of the units had a tuning width of > 120 degrees in contralateral space. Additionally, tuning width increased with stimulation intensity. A significant but considerably scattered topographical order of best azimuth directions was observed in the deep layers of the superior colliculus with frontal directions being represented closer to the rostral pole. Tuned auditory units in the intermediate layers of the superior colliculus, however, showed no systematic spatial arrangement. This pattern was confirmed by analysing best azimuth directions from simultaneously recorded units. Our results indicate that the rat superior colliculus contains a representation of auditory space which is similar to that described for other small mammals.

Acoustic Stimulation↗
PubMed1990

Separating signal and noise in vibrotactile devices for the deaf.

This paper briefly reviews a series of experiments demonstrating that a sound-to-touch transform of signal and noise may be perceptually separated by providing tactile cues for sound localization. Following this, three experiments are reported in which it is shown that such stereotactile cues are available if two vibrotactile devices (Minifonators, produced by Siemens Co. Ltd.), are used instead of one. With this system, subjects were able to attend to a target signal (male voice) in white noise and when a female voice was presented simultaneously. This ability depended upon a sufficient spatial separation of the target and noise in acoustic space. These findings appear to have applications in the design of tactile hearing aids and cochlear implants when used in noisy environments or when more than one sound is present.

Adult↗
PubMed1995

Binaural noise stimulation of auditory callosal fibers of the cat: responses to interaural time delays.

The corpus callosum, the principal neocortical commissure, allows for the interhemispheric transfer of lateralized information between the hemispheres. The aim of the present experiment was to study callosal transfer of auditory information in the cat, with particular reference to its contribution to sound localization. The corpus callosum was approached under direct visual control, and axonic responses were recorded under light anesthesia using glass micro-pipettes. Results showed that auditory information is transmitted in the posterior portion of the callosum. Diotic presentations, in which interaural time delay was manipulated, indicated that, for a large number of fibers, the largest excitatory or inhibitory interactions were obtained at null interaural time delay, a condition which supports the notion of a callosal contribution to auditory midline fusion. However, an important number of callosal fibers was also found to be excited maximally at specific, non-zero interaural time delays, suggesting that they preferred sounds situated at spatial locations other than the midline. The results are discussed in relation to those obtained electrophysiologically for the visual and somesthesic modalities and in terms of results obtained in human and animal behavioral experiments.

Acoustic Stimulation↗
PubMed1986

Directional responses to sounds in young gerbils (Meriones unguiculatus).

Three experiments were conducted to determine the ability of infant gerbils to approach an auditory stimulus. In the first experiment, gerbil pups, 16-23 days of age, were tested in a circular apparatus with a central start area and a movable sound source located at one of eight positions around the perimeter. Stimuli included high- and low-intensity presentations of a tape-recorded gerbil social call, a broad-band white noise stimulus, and a no-stimulus control condition. The subjects showed a strong tendency to approach the low-intensity social call and a less pronounced tendency to approach the white noise. In the second experiment, gerbil pups were tested in the same apparatus with or without ear blocks to determine the role of binaural cues in directional approach responding. The tendency to approach a low-intensity vocalization was disrupted by obstruction of one ear but not by blocking both ears. Thus, binaural balance was shown to be important for early sound localization. In the third experiment, the tendency to approach a social call was compared at different ages, 12-15, 16-19, 20-23, and 24-27 days after birth. Approach responses were first seen at 16-19 days. The responses continued during the 20-23-day period but began to wane at 24-27 days of age.

Animals↗