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PubMed1985

Effects of medial geniculate lesions on sound localization by the rat.

Rats with bilateral lesions of the medial geniculate body were tested on a two-choice sound-localization task that required a directional response to a distant sound source. Stimuli included both broadband and filtered noise bursts presented singly or in repetitive trains. Separate tests were conducted with loudspeakers 180 and 60 degrees apart, centered around 0 degree azimuth. With complete bilateral destruction of the medial geniculate, rats could localize both trains and single bursts of noise and were capable of high levels of performance even at small angles of speaker separation. Some evidence of impaired performance was noted with high-frequency noise bursts, but generally the deficits were not severe. Animals with lesions that extended caudally into the brachium of the inferior colliculus and lateral tegmentum were severely impaired in their ability to localize sounds even at large angles of speaker separation. Three of the four animals in this group were incapable of localizing single bursts even with loudspeakers separated by 180 degrees, and the fourth was unable to perform above chance at 60 degrees. The effects of medial geniculate lesions were very similar to those reported previously for rats with lesions of the auditory cortex, but contrasted with reports of severe impairments in sound localization following damage to the auditory cortex in other mammalian species.

Animals↗
PubMed2002

Sound localization in callosal agenesis and early callosotomy subjects: brain reorganization and/or compensatory strategies.

In order to evaluate the callosal involvement in sound localization, the present study examined the response accuracy of acallosal and early callosotomized subjects to monaural and binaural auditory targets presented in three-dimensional space. In these subjects, bilateral localization cues, such as interaural time and level differences, are integrated at the cortical and subcortical levels without the additional support of the callosal commissure. Because acallosal and early-callosotomized subjects have developed with this reduced source of binaural activation of cortical cells, they might have perfected their ability to use monaural sound localization cues. This hypothesis was tested by assessing localization performance under both binaural and monaural listening conditions. Five subjects with callosal agenesis, one callosotomized subject operated early in life and 19 control subjects were asked to localize broad-band noise bursts (BBNBs) of fixed intensity in the horizontal plane in an anechoic chamber. BBNBs were delivered through randomly selected loudspeakers. Two conditions were tested: (i) localization of a stationary sound source; and (ii) localization of a moving sound source. Listeners had to report the apparent stimulus location by pointing to its perceived position on a graduated perimeter. The results indicated that the acallosal subjects were less accurate than controls, but only in the binaural moving sound condition. More interestingly, in the monaural testing conditions, some of the acallosal subjects and the early-callosotomized subject performed significantly better than control subjects. This suggests that, because of the absence of the corpus callosum, these subjects compensate for their reduced access to cortically determined binaural cues by making more efficient use of monaural cues.

Acoustic Stimulation↗
PubMed1990

Tests of the precedence effect in sound localization reveal abnormalities in multiple sclerosis.

The precedence effect in sound localization involves presenting identical sounds (e.g., clicks) from pairs of matched speakers situated on opposite sides of a subject's head, with the clicks from one speaker preceding those from the other by a short interval. With appropriate delays, normal subjects perceive a fused image which originates from the side of the leading speaker. This test was administered to 24 patients with multiple sclerosis (MS). Separate tests involving speaker delays ranging from 0 msec (simultaneous presentation) to 8 msec were presented. At 0 msec delay, normal subjects perceived the fused image to be located halfway between the two speakers; at progressively longer delays, the image was perceived closer to the leading speaker. In contrast to normal subjects, a large proportion of the MS subjects exhibited difficulties with the task. The discrimination deficit was limited to delays below 1 msec, suggesting a problem involving an increased threshold for lateralizing the fused image away from midline toward the side of the leading speaker. The neural instability produced by demyelination in MS patients might account for this pattern of results.

Adult↗
PubMed2001

Effects of stimulus intensity on sound localization in the horizontal and upper-hemispheric median plane.

Sound lateralization ability with headphones is known to be affected by stimulus intensity. However, there have been few studies on sound localization with loudspeakers in free field from the standpoint of stimulus intensity. The aim of this study is to obtain basic data for the tests with normal hearing and hearing-impaired subjects, and for the fitting of a hearing aid. The author investigated the relationship between stimulus intensities and sound localization ability of the broadband noise and pure tone bursts delivered in the horizontal and upper-hemispheric median planes. Subjects were ten volunteers, 5 males and 5 females, at the age of 18-19 years, with normal hearing. The results showed well how subjects perceived directions at all stimulus intensities. The percentage of correct response (%correct) for broadband noise stimuli was maximum at the intensity from 40 to 70 dB SPL (sound pressure level), and was minimum at 0 to 20 dB SPL in both the horizontal plane and the upper-hemispheric median plane. At lower stimulus intensity, examinee could not judge the direction, even if they could hear the stimuli. For pure tone bursts stimuli in the upper-hemispheric median plane, %correct was low irrespective of stimulus intensity.

Acoustic Stimulation↗
PubMed1984

Role of cat primary auditory cortex for sound-localization behavior.

Small lesions designed to completely destroy the cortical zone of representation of a restricted band of frequency were introduced within the primary auditory cortex (AI) in adult cats. Physiological mapping was used to guide placement of lesions. Sound-localization performance was evaluated prior to and after induction of these lesions in a seven-choice free-sound-field apparatus. All tested cats had profound contralateral hemifield deficits for the localization of brief tones at frequencies roughly corresponding to those whose representations were destroyed by the lesion. Sound-localization performance was normal at all other test frequencies. In a single adult cat, a massive lesion destroyed nearly all auditory cortex unilaterally, with only the representation of a narrow band of frequency within AI spared by the lesion. This cat had normal abilities for azimuthal sound localization across that frequency band but a profound contralateral deficit for the azimuthal localization of brief sounds at all other frequencies. Recorded sound-localization deficits were permanent. Localization of long-duration tones was not affected by a unilateral AI lesion. These studies indicate that, at least in cats, AI is necessary for normal binaural sound-localization behavior; among auditory cortical fields, AI is sufficient for normal binaural sound-localization behavior; sound-location representation is organized by frequency channel in the auditory forebrain; and AI in each hemisphere contributes to only contralateral free-sound-field location representation.

Animals↗
PubMed1990

An evaluation of an in vivo local sound speed estimation technique by the crossed beam method.

An in vivo local sound speed estimation technique, using the crossed beam method, has been proposed and its applicability was evaluated. At first, the potential of this technique was studied by a mapping simulation using the ray tracing technique followed by an experiment with a cylindrical agar phantom. The simulation result showed that an exact measurement of local sound speed values was difficult, but the sound speed information for the local region (its relative magnitude to the surrounding medium) was emphasized as a refraction mapping pattern. The experimental results agreed well with the calculation results. Furthermore, a clinical application was performed, using the clinical system (modified electronic linear scanner), on two liver tumor patients.

Acoustics↗
PubMed2005

High binaural coherence determines successful sound localization and increased activity in posterior auditory areas.

Our brain continuously receives complex combinations of sounds originating from different sources and relating to different events in the external world. Timing differences between the two ears can be used to localize sounds in space, but only when the inputs to the two ears have similar spectrotemporal profiles (high binaural coherence). We used fMRI to investigate any modulation of auditory responses by binaural coherence. We assessed how processing of these cues depends on whether spatial information is task relevant and whether brain activity correlates with subjects' localization performance. We found that activity in Heschl's gyrus increased with increasing coherence, irrespective of whether localization was task relevant. Posterior auditory regions also showed increased activity for high coherence, primarily when sound localization was required and subjects successfully localized sounds. We conclude that binaural coherence cues are processed throughout the auditory cortex and that these cues are used in posterior regions for successful auditory localization.

Acoustic Stimulation↗
PubMed2004

Contrasting monaural and interaural spectral cues for human sound localization.

A human psychoacoustical experiment is described that investigates the role of the monaural and interaural spectral cues in human sound localization. In particular, it focuses on the relative contribution of the monaural versus the interaural spectral cues towards resolving directions within a cone of confusion (i.e., directions with similar interaural time and level difference cues) in the auditory localization process. Broadband stimuli were presented in virtual space from 76 roughly equidistant locations around the listener. In the experimental conditions, a "false" flat spectrum was presented at the left eardrum. The sound spectrum at the right eardrum was then adjusted so that either the true right monaural spectrum or the true interaural spectrum was preserved. In both cases, the overall interaural time difference and overall interaural level difference were maintained at their natural values. With these virtual sound stimuli, the sound localization performance of four human subjects was examined. The localization performance results indicate that neither the preserved interaural spectral difference cue nor the preserved right monaural spectral cue was sufficient to maintain accurate elevation judgments in the presence of a flat monaural spectrum at the left eardrum. An explanation for the localization results is given in terms of the relative spectral information available for resolving directions within a cone of confusion.

Acoustic Stimulation↗
PubMed1976

Sound localization in anurans. I. Evidence of binaural interaction in dorsal medullary nucleus of bullfrogs (Rana catesbeiana).

1. The response patterns of single cells to monaural and binaural acoustic stimuli were studied in the dorsal medullary nucleus of the bullfrog (Rana catesbeiana). This nucleus represents the first ascending center in the anuran's central auditory nervous system. 2. Of the 142 cells isolated, 75 units responded only to monaural stimulation. Approximately 80% of these monaural cells could be excited by the ipsilateral ear, while the remaining 20% received their excitatory input from the contralateral ear. The other 67 units responded to binaural stimuli. Of these binaural cells, 14 could be excited by either contralateral or ipsilateral stimuli, and the threshold and best excitatory frequency were similar for each ear (EE). The other 53 binaural cells (EI) could be excited by stimulation of one ear and inhibited by stimulation of the other ear; for almost all of these cells the contralateral ear was excitatory and the ipsilateral ear was inhibitory. The best inhibitory frequency for one ear was approximately the same as the best excitatory frequency for the other ear, and the threshold for inhibition was near the threshold for excitation. 3. The tuning curves for all of the cells in the dorsal medullary nucleus were unimodal with "Q" values ranging from 0.4 to 4. The excitatory thresholds were widely scattered between 22 and 115 dB SPL. 4. The distribution of best excitatory frequencies for the monaural cells comprised three groups: 200-300, 500-800, and 900-1,600 Hz. The best excitatory frequencies of the binaural cells were scattered over this entire range, with a broad peak around 200-800 Hz. 5. Approximately 80% of the cells in the dorsal nucleus responded tonically throughout the duration of an excitatory tone burst. The remaining 20% of the cells responded phasically during the transient stages of a tone burst over a wide intensity range. 6. Response latencies were compared for the two types of monaural cells to tones at their best exciatatory frequencies at 10 dB above threshold. The latencies for the contralaterally excitable cells were just a few milliseconds longer than the latencies for the ipsilaterally excitable cells. For binaural cells the latency for contralateral stimulation was only 1-2 ms longer than for ipsilateral stimulation. It was concluded that the contralateral input to the dorsal medullary nucleus is not of efferent descending origin from higher auditory centers. 7. All of the binaural EI cells were sensitive to small interaural intensity differences and many were also sensitive to minute interaural time differences. These cells likely play a role in localization of sounds of significance to anurans.

Action Potentials↗
PubMed1980

Horizontal sound localization skills of unilaterally hearing-impaired children.

The present study assessed the horizontal sound localization skills of three groups of subjects; normal-hearing adults, normal-hearing children, and unilaterally hearing-impaired children. The ability of these subjects to localize pure tones to 500 and 3000 Hz in quiet and in a background of cafeteria noise was evaluated using an array of thirteen loudspeakers mounted in a large anechoic chamber. Results indicated a significant effect of signal frequency in all three groups of listeners. In addition, the hearing-impaired children performed significantly poorer than their normal-hearing counterparts in all conditions. Individual differences in sound localization ability among the hearing-impaired listeners could be explained largely through effects of age and degree of hearing impairment.

Adolescent↗
PubMed1975

The accuracy of diver sound localization by pointing.

The accuracy of human sound localization in 360 degrees of azimuth was determined underwater in a free field. The location indicator was a pointer in the median plane. Accuracy of the response was defined as the mean deviation (MD) from the objective location of a sound source. Maximum accuracy obtained using the present procedure with visual cues was approximately 6 degrees, while maximum accuracy with auditory cues was approximately 11 degrees. Training with visual feedback resulted in a reduction in errors due to the pointing procedure employed, but did not affect localization accuracy. The decrement in accuracy of auditory localization found in the water environment should have no noticeable effect on the ability of divers to find a sound source in the environment.

Adult↗
PubMed1997

Monaural sound localization revisited.

Research reported during the past few decades has revealed the importance for human sound localization of the so-called "monaural spectral cues." These cues are the result of the direction-dependent filtering of incoming sound waves accomplished by the pinnae. One point of view about how these cues are extracted places great emphasis on the spectrum of the received sound at each ear individually. This leads to the suggestion that an effective way of studying the influence of these cues is to measure the ability of listeners to localize sounds when one of their ears is plugged. Numerous studies have appeared using this monaural localization paradigm. Three experiments are described here which are intended to clarify the results of the previous monaural localization studies and provide new data on how monaural spectral cues might be processed. Virtual sound sources are used in the experiments in order to manipulate and control the stimuli independently at the two ears. Two of the experiments deal with the consequences of the incomplete monauralization that may have contaminated previous work. The results suggest that even very low sound levels in the occluded ear provide access to interaural localization cues. The presence of these cues complicates the interpretation of the results of nominally monaural localization studies. The third experiment concerns the role of prior knowledge of the source spectrum, which is required if monaural cues are to be useful. The results of this last experiment demonstrate that extraction of monaural spectral cues can be severely disrupted by trial-to-trial fluctuations in the source spectrum. The general conclusion of the experiments is that, while monaural spectral cues are important, the monaural localization paradigm may not be the most appropriate way to study their role.

Auditory Perception↗
PubMed1998

Passive sound-localization ability of the big brown bat (Eptesicus fuscus).

The passive sound-localization ability (i.e. minimum audible angle) of the big brown bat, Eptesicus fuscus, was determined using a conditioned avoidance procedure in which the animals were trained to discriminate left sounds from right sounds. The mean threshold of three bats for a 100-ms broadband noise burst was 14 degrees, a value that is about average for mammals. A similar threshold of 15 degrees was obtained for one animal when it was retested with one of its own recorded echolocation calls as the stimulus. The two bats tested on pure-tone localization were able to localize high-frequency, but not low-frequency tones, even when a low-frequency tone was amplitude modulated, a result indicating that these bats are not able to use binaural time-difference cues for localization. Finally, given the width of the bat's field of best vision, as determined by a count of its ganglion-cell density, its sound-localization acuity is consistent with the hypothesis that the role of passive sound localization is to direct the eyes to the source of a sound.

Acoustic Stimulation↗
PubMed1986

Midline and lateral field sound localization in the albino rat (Rattus norvegicus).

Six albino rats were used in tests of sound localization around midline and in left and right lateral field positions (i.e., 0 degree, -60 degrees, and +60 degrees azimuth). Each of the animals performed at high levels on the midline task but had great difficulty with tests in the left and right fields. Minimum audible angles for midline localization were obtained for 2 subjects and were estimated as 11.5 degrees and 13.5 degrees. Performance levels on the hemifield tests for each of the 6 animals, however, were too low to permit estimates of threshold even with speakers separated by 60 degrees. The differences between midline and lateral field sound localization are discussed.

Animals↗
PubMed2000

Neural system identification model of human sound localization.

This paper examines the role of biological constraints in the human auditory localization process. A psychophysical and neural system modeling approach was undertaken in which performance comparisons between competing models and a human subject explore the relevant biologically plausible "realism constraints." The directional acoustical cues, upon which sound localization is based, were derived from the human subject's head-related transfer functions (HRTFs). Sound stimuli were generated by convolving bandpass noise with the HRTFs and were presented to both the subject and the model. The input stimuli to the model were processed using the Auditory Image Model of cochlear processing. The cochlear data were then analyzed by a time-delay neural network which integrated temporal and spectral information to determine the spatial location of the sound source. The combined cochlear model and neural network provided a system model of the sound localization process. Aspects of humanlike localization performance were qualitatively achieved for broadband and bandpass stimuli when the model architecture incorporated frequency division (i.e., the progressive integration of information across the different frequency channels) and was trained using variable bandwidth and center-frequency sounds. Results indicate that both issues are relevant to human sound localization performance.

Adult↗
PubMed2006

Spike-timing codes enhance the representation of multiple simultaneous sound-localization cues in the inferior colliculus.

To preserve multiple streams of independent information that converge onto a neuron, the information must be re-represented more efficiently in the neural response. Here we analyze the increase in the representational capacity of spike timing over rate codes using sound localization cues as an example. The inferior colliculus receives convergent input from multiple auditory brainstem nuclei, including sound localization information such as interaural level differences (ILDs), interaural timing differences (ITDs), and spectral cues. Virtual space techniques were used to create stimulus sets varying in two sound-localization parameters each. Information about the cues was quantified using a spike distance metric that allows one to separate contributions to the information arising from spike rate and spike timing. Spike timing enhances the representation of spectral and ILD cues at timescales averaging 12 ms. ITD information, however, is carried by a rate code. Comparing responses to frozen and random noise shows that the temporal information is mainly attributable to phase locking to temporal stimulus features, with an additional first-spike latency component. With rate-based codes, there is significant confounding of information about two cues presented simultaneously, meaning that the cues cannot be decoded independently. Spike-timing-based codes reduce this confounded information. Furthermore, the relative representation of the cues often changes as a function of the time resolution of the code, implying that information about multiple cues can be multiplexed onto individual spike trains.

Acoustic Stimulation↗
PubMed2003

Plasticity in human sound localization induced by compressed spatial vision.

Auditory and visual target locations are encoded differently in the brain, but must be co-calibrated to maintain cross-sensory concordance. Mechanisms that adjust spatial calibration across modalities have been described (for example, prism adaptation in owls), though rudimentarily in humans. We quantified the adaptation of human sound localization in response to spatially compressed vision (0.5x lenses for 2-3 days). This induced a corresponding compression of auditory localization that was most pronounced for azimuth (minimal for elevation) and was restricted to the visual field of the lenses. Sound localization was also affected outside the field of visual-auditory interaction (shifted centrally, not compressed). These results suggest that spatially modified vision induces adaptive changes in adult human sound localization, including novel mechanisms that account for spatial compression. Findings are consistent with a model in which the central processing of sound location is encoded by recruitment rather than by a place code.

Acoustic Stimulation↗