Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Sound Localization”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

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

At least 181 records · Page 10Linked to original sources

Comparative physiology of sound localization in four species of owls.

Bilateral ear asymmetry is found in some, but not all, species of owls. We investigated the neural basis of sound localization in symmetrical and asymmetrical species, to deduce how ear asymmetry might have evolved from the ancestral condition, by comparing the response properties of neurons in the external nucleus of the inferior colliculus (ICx) of the symmetrical burrowing owl and asymmetrical long-eared owl with previous findings in the symmetrical great horned owl and asymmetrical barn owl. In the ICx of all of these owls, the neurons had spatially restricted receptive fields, and auditory space was topographically mapped. In the symmetrical owls, ICx units were not restricted in elevation, and only azimuth was mapped in ICx. In the barn owl, the space map is two-dimensional, with elevation forming the second dimension. Receptive fields in the long-eared owl were somewhat restricted in elevation, but their tuning was not sharp enough to determine if elevation is mapped. In every species, the primary cue for azimuth was interaural time difference, although ICx units were also tuned for interaural intensity difference (IID). In the barn owl, the IIDs of sounds with frequencies between about 5 and 8 kHz vary systematically with elevation, and the IID selectivity of ICx neurons primarily encodes elevation. In the symmetrical owls, whose ICx neurons do not respond to frequencies above about 5 kHz, IID appears to be a supplementary cue for azimuth. We hypothesize that ear asymmetry can be exploited by owls that have evolved the higher-frequency hearing necessary to generate elevation cues. Thus, the IID selectivity of ICx neurons in symmetrical owls may preadapt them for asymmetry; the neural circuitry that underlies IID selectivity is already present in symmetrical owls, but because IID is not absolutely required to encode azimuth it can come to encode elevation in asymmetrical owls.

Animals↗

The lateral superior olive: a functional role in sound source localization.

Sound location in azimuth is signaled by differences in the times of arrival (interaural time difference, ITDs) and the amplitudes (interaural level differences, ILDs) of the stimuli at the ears. Psychophysical studies have shown that low- and high-frequency sounds are localized based on ITDs and ILDs, respectively, suggesting that dual mechanisms mediate localization. The anatomical and physiological bases for this "duplex theory" of localization are found in the medial (MSO) and lateral (LSO) superior olives, two of the most peripheral sites in the ascending auditory pathway receiving inputs from both ears. The MSO and LSO are believed to be responsible for the initial encoding of ITDs and ILDs, respectively. Here the author focuses on ILDs as a cue to location and the role of the LSO in encoding ILDs. Evidence from disparate fields of study supports the hypothesis that the LSO is the initial ILD processor in the mammalian auditory system.

Animals↗

The effect of the audallion BEAMformer noise reduction preprocessor on sound localization for cochlear implant users.

OBJECTIVE: To assess the effect of the Audallion BEAMformer noise reduction preprocessor on the sound localization ability of children fitted unilaterally with the Nucleus 22-channel cochlear implant. DESIGN: Eight children aged 11 to 14 yr participated. Using three arrays of six loudspeakers, each child was tested in a semi-reverberant sound proof booth representative of a small office environment. The six loudspeakers were positioned 30 degrees apart in the horizontal plane at a distance of 1 m, spanning 150 degrees either directly in front of or to the left or right of the subject. The stimulus to be localized was a 300 msec broadband noise with a rise/decay of 50 msec. Subjects were tested with the BEAMformer in four possible settings, including one single microphone control condition, with each of the three loudspeaker arrays. One block of 60 forced-choice speaker identification trials was presented for each of the 12 listening conditions. On each trial, the stimulus was emitted by one of the six loudspeakers, randomly selected. RESULTS: Results demonstrated that subjects were unable to discriminate among sound sources arrayed horizontally in space using the cochlear implant microphone alone, or in combination, with the BEAMformer microphone located on the other ear. Results also showed that using the BEAMformer did not bias the perception of spatial location. CONCLUSIONS: The localization of acoustic stimuli in pediatric cochlear implant users was unaffected by the use of the Audallion BEAMformer. The apparent origin of most sounds appears to be pulled toward the implanted ear. Further studies are needed to validate findings.

Acoustic Stimulation↗

The effect of eye position and background noise on vertical sound localization.

The influence of the eye position in combination with a simultaneously presented background (frame) sound on the auditory localization of a single (target) sound source was investigated in the median vertical plane (MVP). Five loudspeakers ranged from -20 degrees to +20 degrees with the center speaker at 0 degrees elevation. Listeners verbally estimated the position of a 500-ms noise stimulus, which was presented while they were fixating visual targets in various elevations. The perceived sound elevation appeared to be shifted 8.6 degrees on average towards the direction of eccentric gaze. When the target was temporarily embedded in a 2-s frame sound (emitted by one of the two outer loudspeakers) and the gaze was fixated at a straight-ahead position, the listeners consistently shifted the apparent target positions about 4 degrees away from the frame locations. This auditory contrast effect, which is consistent with earlier findings, remained even if the gaze direction deviated from straight ahead. It is concluded that the auditory contrast effect exists independently from the eye position effect and that the two effects act separately on auditory sound localization.

Acoustic Stimulation↗

Neural network models of sound localization based on directional filtering by the pinna.

Three-layer neural-network functions were developed to transform spectral representations of pinna-filtered stimuli at the input to a space-mapped representation of sound-source direction at the output. The inputs are modeled after transfer functions of the external ear of the cat; the output is modeled on the spatial sensitivity of superior colliculus neurons. Network solutions are obtained by backpropagation and by a method that enforces uniform task distribution in the hidden layer of the model. Solutions are characterized using bandlimited inputs to study the relative strength of potential sound localization cues in various frequency regions. This analysis suggests that the frequency region containing the first spectral notch (5-18 kHz) provides the best localization cues. Response properties of model neurons were studied using input patterns modeled after auditory nerve response profiles to pure tones at various frequencies and sound levels. The response properties of hidden layer model neurons resemble cochlear nucleus types III and IV and their composites. Neurons in both hidden and output layers show the properties of spectral notch detectors. Although neural networks have limitations as models of real neural systems, the results illustrate how they can provide insight into the computation of complex transformations in the nervous system.

Auditory Perception↗

The owl's cochlear nuclei process different sound localization cues.

This paper discusses how the barn owl's brain stem auditory pathway is divided into two physiologically and anatomically segregated channels for separate processing of interaural phase and intensity cues for sound localization. The paper also points out the power of the "downstream" approach by which the emergence of a higher-order neuron's stimulus selectivity can be traced through lower-order stations.

Animals↗

Behavioral studies of sound localization in the cat.

Using the magnetic search coil technique to measure eye and ear movements, we trained cats by operant conditioning to look in the direction of light and sound sources with their heads fixed. Cats were able to localize noise bursts, single clicks, or click trains presented from sources located on the horizontal and vertical meridians within their oculomotor range. Saccades to auditory targets were less accurate and more variable than saccades to visual targets at the same spatial positions. Localization accuracy of single clicks was diminished compared with the long-duration stimuli presented from the same sources. Control experiments with novel auditory targets, never associated with visual targets, demonstrated that the cats localized the sound sources using acoustic cues and not from memory. The role of spectral features imposed by the pinna for vertical sound localization was shown by the breakdown in localization of narrow-band (one-sixth of an octave) noise bursts presented from sources along the midsagittal plane. In addition, we show that cats experience summing localization, an illusion associated with the precedence effect. Pairs of clicks presented from speakers at (+/-18 degrees,0 degrees ) with interclick delays of +/-300 microsec were perceived by the cat as originating from phantom sources extending from the midline to approximately +/-10 degrees.

Acoustic Stimulation↗

Correlated cortical populations can enhance sound localization performance.

Neurons within cortical populations often evidence some degree of response correlation. Correlation has generally been regarded as detrimental to the decoding performance of a theoretical vector-averaging observer making inferences about the physical world-for example, an observer estimating the location of a sound source. However, if an alternative decoder is considered, in this case a Maximum Likelihood estimator, performance can improve when responses in the population are correlated. Improvement in sound localization performance is demonstrated analytically using Fisher information, and is also shown using Monte Carlo simulations based on recordings from single neurons in cat primary auditory cortex.

Animals↗

Sound localization. The interaction of aging, hearing loss and hearing protection.

The effect of conventional ear plugs and ear muffs, and muffs with limited dichotic amplification on the ability to localize one-third octave noise bands was investigated under semi-reverberant listening conditions. Forty-eight normal-hearing subjects, half over 40 years of age, and 23 subjects with bilateral sensorineural hearing loss participated. Sound localization was assessed using an array of six loudspeakers surrounding the subject at azimuth angles 60 degrees apart. One block of 120 forced-choice speaker identification trials was presented for each of 16 listening conditions defined by ear condition (unoccluded, E-A-R plug, E-A-R muff, and Bilsom 2392 muff), stimulus frequency (500 Hz and 4000 Hz), and background (quiet and continuous 65 dB SPL-white noise). Plugs and muffs, particularly active muffs, resulted in decrements in right/left judgments based on interaural intensity but not time-of-arrival differences. High-frequency front/back discrimination was affected more by muffs than by plugs. Error patterns for the conventional and active muffs were dissimilar. Aging resulted in a decrement in unoccluded front/back discrimination. Trends for the impaired subjects were the same as those for normal subjects at 500 Hz. Many could not hear 4000 Hz with conventional protectors. Their performance was no different from normal with the active muffs.

Adolescent↗

Monitoring the environment: sound localization equipment for deaf-blind people.

The problems that deaf-blind subjects have with monitoring the environment and the strategies they use were identified using structured interviews. The use of the vibratory sense did not appear to be highly developed, but some individuals indicated that it has great potential. We describe here the design of a computerized laboratory device for sound localization, based on a three-microphone system with a cross correlation algorithm. It was found to have reasonable precision and sufficient reliability to allow the detection and localization of a person approaching a deaf-blind subject in an ordinary room. The next step is to miniaturize the equipment and build a portable prototype.

Algorithms↗

Sound localization: effects of reverberation time, speaker array, stimulus frequency, and stimulus rise/decay.

This research assessed the ability of human listeners to localize one-third octave noise bands in the horizontal plane. The effects of reverberation time (absorbent versus reverberant room), stimulus center frequency (500, 1000, 2000, and 4000 Hz), stimulus rise/decay time (5 vs 200 ms) and speaker array (frontal versus lateral) were investigated for four subjects using a forced-choice speaker-identification paradigm. Sound localization scores were consistently lower in the reverberant room than in the absorbent room. They also revealed strong frequency and azimuthal effects. The benefit of a shorter rise/decay time was small and limited to low frequencies. The identification of a speaker position depended strongly upon the array in which it was embedded, primarily because localization in the lateral array led to frequency-dependent front/back confusions and response bias. The results also illustrated the importance of choosing a coordinate system based on the auditory cone-of-confusion to analyze localization data for speaker arrays spanning the aural axis.

Auditory Perception↗

Shift in sound localization induced by rTMS of the posterior parietal lobe.

Neuroimaging studies in human subjects and single-unit recordings in monkeys have suggested the primate posterior parietal cortex (PPC) to be involved in auditory space perception. Here we tested this hypothesis by combining repetitive focal transcranial magnetic stimulation (rTMS) of the right PPC with a task of pointing to free-field-sound stimuli. After a period of 15 min rTMS at 1Hz, subjects exhibited an overall signed error in pointing by 2.5 degrees, directed to the left and downward, with reference to a baseline condition with "sham rTMS". No effects of rTMS on the general precision of sound localization (unsigned errors) were found. Thus, low-frequency offline rTMS may have specifically affected neuronal circuits transforming auditory spatial coordinates in both azimuth and elevation. This is in accordance with the view that the PPC may represent a neural substrate of the perceptual stability in spatial hearing.

Acoustic Stimulation↗

Active stereo sound localization.

Estimating the direction of arrival of sound in three-dimensional space is typically performed by generalized time-delay processing on a set of signals from a fixed array of omnidirectional microphones. This requires specialized multichannel A/D hardware, and careful arrangement of the microphones into an array. This work is motivated by the desire to instead only use standard two-channel audio A/D hardware and portable equipment. To estimate direction of arrival of persistent sound, the position of the microphones is made variable by mounting them on one or more computer-controlled pan-and-tilt units. In this paper, we describe the signal processing and control algorithm of a device with two omnidirectional microphones on a fixed baseline and two rotational degrees of freedom. Experimental results with real data are reported with both impulsive and speech sounds in an untreated, normally reverberant indoor environment.

Algorithms↗

Sound localization in the human brain: neuromagnetic observations.

Sound location processing in the human auditory cortex was studied with magnetoencephalography (MEG) by producing spatial stimuli using a modern stimulus generation methodology utilizing head-related transfer functions (HRTFs). The stimulus set comprised wideband noise bursts filtered through HRTFs in order to produce natural spatial sounds. Neuromagnetic responses for stimuli representing eight equally spaced sound source directions in the azimuthal plane were measured from 10 subjects. The most prominent response, the cortically generated N1m, was investigated above the left and right hemisphere. We found, firstly, that the HRTF-based stimuli presented from different directions elicited contralaterally prominent N1m responses. Secondly, we found that cortical activity reflecting the processing of spatial sound stimuli was more pronounced in the right than in the left hemisphere.

Acoustic Stimulation↗

Simulated motion enhances neuronal selectivity for a sound localization cue in background noise.

In nature, sound sources move and signals are accompanied by background noise. Noting that motion helps the perception of visual stimuli, we tested whether motion similarly facilitates the detection of acoustic targets, at the neuronal level. Auditory neurons in the central nucleus of the barn owl's inferior colliculus (ICc), due to their selectivity for interaural phase difference (delta phi), are sharply tuned to the azimuth of sound sources and are arrayed to form a topographic map of delta phi. While recording from single ICc neurons, we presented tones that simulated either moving or stationary sound sources with and without background noise. We found that the tuning of cells in the ICc for delta phi was sharper for stimuli that simulated motion than for those that simulated stationary targets. The neurons signaled the presence of a tone obscured by noise better if the tone moved than if the tone remained stationary. The resistance to noise observed with moving stimuli could not be reproduced with the temporal modulation of the stimulus amplitude, suggesting that a change of position over time was required.

Acoustic Stimulation↗

Binaural response organization within a frequency-band representation of the inferior colliculus: implications for sound localization.

The auditory system of the mustache bat (Pteronotus parnellii) contains a disproportionately large representation of a narrow frequency band, corresponding to the dominant, 60 kHz component of its echolocation signal. In the inferior colliculus (IC), the 60 kHz representation comprises an architectonically distinct region called the dorsoposterior division (DPD), which is accessible for detailed physiological study. We examined the topographic distribution of binaural responses within this one frequency-band representation of the inferior colliculus. We describe two primary results. First, neurons with different binaural response properties are spatially segregated into one of four binaural response-specific regions of the DPD: a large region of monaural (EO) responses; two regions containing neurons excited by sound from both ears (EE); and a region containing neurons excited by one ear and inhibited by the other (EI). Regions dominated by 60 kHz EI responses are also found in the lateral extremity of the IC, probably within the external nucleus. These results demonstrate functionally defined subdivisions in a single frequency-band representation of the IC. Moreover, they suggest that brain stem auditory projections to the DPD and/or intrinsic connections within the DPD are highly organized. Second, within the EI region of the DPD, there is a systematic shift in the sensitivity of EI multiunit responses to interaural intensity disparities (IIDs). Dorsally, EI neurons are suppressed only by relatively loud ipsilateral sounds, and there is a systematic decrease in the relative ipsilateral intensity required for suppression at more ventral recording sites. This result demonstrates that neurons sensitive to a sound localization cue are systematically organized within a frequency-band representation of the inferior colliculus. It has implications for the manner in which the location of a sound source is encoded within the primary auditory pathway.

Animals↗

[Influence of visual attention upon sound localization].

Previous studies on audio-visual interaction such as the ventriloquism effect have indicated cognitive (or context) factors as well as sensory (or synchronous) factors could make the interaction. In these studies, however, visual attention seems to have been neglected. Thus, it has been still unknown whether the visual attention affects the interaction or not. We investigated the contribution of the attention factors to the audio-visual interaction by comparing the sound localization biases made by attentional factors and those by synchronous factors. Three subjects participated in the localization tasks in horizontal and vertical orientations. As the results, we found small influence of the attentional factors upon the interaction in the horizontal orientation, and no influence in the vertical orientation. On the contrary, the effect of the synchronous factors was larger in the vertical orientation than in the horizontal orientation. We concluded that the visual attention could affect the audio-visual interaction slightly, and that the influences of the attentional factors and the perceptual factors upon the interactions were made in the different processes.

Attention↗