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Sound localization for a virtual sound source in cases of chronic otitis media.

Sound localization in subjects with chronic otitis media (COM) was examined before and soon after ear surgery by means of virtual sound presented by headphones, sound being synthesized based on the head-related transfer functions (HRTFs) in a normal subject. The localization ability in COM patients was usually worse than that in normal subjects, but was better than expected when compared with cases of acute loss. On the other hand, the effects of hearing improvement on localization ability observed in COM patients were smaller than those of simulated acute hearing loss achieved by earplugs in normal subjects. This seems to suggest that the localization cues in patients with chronic hearing loss are different from those under normal conditions.

Adult↗

A robust method for heart sounds localization using lung sounds entropy.

Heart sounds are the main unavoidable interference in lung sound recording and analysis. Hence, several techniques have been developed to reduce or cancel heart sounds (HS) from lung sound records. The first step in most HS cancellation techniques is to detect the segments including HS. This paper proposes a novel method for HS localization using entropy of the lung sounds. We investigated both Shannon and Renyi entropies and the results of the method using Shannon entropy were superior. Another HS localization method based on multiresolution product of lung sounds wavelet coefficients adopted from was also implemented for comparison. The methods were tested on data from 6 healthy subjects recorded at low (7.5 ml/s/kg) and medium 115 ml/s/kg) flow rates. The error of entropy-based method using Shannon entropy was found to be 0.1 +/- 0.4% and 1.0 +/- 0.7% at low and medium flow rates, respectively, which is significantly lower than that of multiresolution product method and those of other methods reported in previous studies. The proposed method is fully automated and detects HS included segments in a completely unsupervised manner.

Adult↗

The influence of duration and level on human sound localization.

The localization of sounds in the vertical plane (elevation) deteriorates for short-duration wideband sounds at moderate to high intensities. The effect is described by a systematic decrease of the elevation gain (slope of stimulus-response relation) at short sound durations. Two hypotheses have been proposed to explain this finding. Either the sound localization system integrates over a time window that is too short to accurately extract the spectral localization cues (neural integration hypothesis), or the effect results from cochlear saturation at high intensities (adaptation hypothesis). While the neural integration model predicts that elevation gain is independent of sound level, the adaptation hypothesis holds that low elevation gains for short-duration sounds are only obtained at high intensities. Here, these predictions are tested over a larger range of stimulus parameters than has been done so far. Subjects responded with rapid head movements to noise bursts in the two-dimensional frontal space. Stimulus durations ranged from 3 to 100 ms; sound levels from 26 to 73 dB SPL. Results show that the elevation gain decreases for short noise bursts at all sound levels, a finding that supports the integration model. On the other hand, the short-duration gain also decreases at high sound levels, which is in line with the adaptation hypothesis. The finding that elevation gain was a nonmonotonic function of sound level for all sound durations, however, is predicted by neither model. It is concluded that both mechanisms underlie the elevation gain effect and a conceptual model is proposed to reconcile these findings.

Adult↗

Enhanced sound localization.

A new approach to sound localization, known as enhanced sound localization, is introduced, offering two major benefits over state-of-the-art algorithms. First, higher localization accuracy can be achieved compared to existing methods. Second, an estimate of the source orientation is obtained jointly, as a consequence of the proposed sound localization technique. The orientation estimates and improved localizations are a result of explicitly modeling the various factors that affect a microphone's level of access to different spatial positions and orientations in an acoustic environment. Three primary factors are accounted for, namely the source directivity, microphone directivity, and source-microphone distances. Using this model of the acoustic environment, several different enhanced sound localization algorithms are derived. Experiments are carried out in a real environment whose reverberation time is 0.1 seconds, with the average microphone SNR ranging between 10-20 dB. Using a 24-element microphone array, a weighted version of the SRP-PHAT algorithm is found to give an average localization error of 13.7 cm with 3.7% anomalies, compared to 14.7 cm and 7.8% anomalies with the standard SRP-PHAT technique.

Algorithms↗

Two-dimensional sound-localization behavior of early-blind humans.

To investigate whether the visual system is crucial for adequate calibration of acoustic localization cues, sound-localization performance of early blind humans was compared with that of sighted controls. Because a potential benefit of vision is mainly expected for targets within the two-dimensional (2D) frontal hemifield, localization was tested within this target range, while using sounds of various durations and spectral content. Subjects were instructed to point, in separate experimental sessions, either with their left arm, or with their nose, in the direction of the perceived target position as accurately as possible. The experiments required the use of all available sound-localization cues such as interaural differences in phase and intensity, as well as the complex spectral shape cues provided by the pinnae. In addition, for long-duration stimuli, subjects could have had access to head motion-induced acoustic feedback. Moreover, the two pointing methods allowed us to assess different response strategies for the two groups. In an additional series, subjects were instructed to respond as quickly as possible. The results show that, in general, 2D sound-localization performance of blind subjects was indistinguishable from that of sighted subjects, both for broad-band noise and for pure tones. In the fast head-pointing task, the latency distributions of both groups were equal. These findings suggest that visual feedback is not required to calibrate the available localization cues--including the idiosyncratic and complex spectral shape cues for elevation. Instead, the localization abilities of blind people show that the putative supervising role of vision may be supported, or taken over, by other non-visual feedback systems. The results do not provide support for the hypothesis that blind people can hypercompensate for the loss of vision in the frontal hemifield by developing superior sound-localization abilities. Despite the general correspondence in localization behavior, some specific differences related to pointing strategies as well as to those between blind and sighted subjects were apparent. Most importantly, the reconstructed origin (bias) of arm pointing was located near the shoulder for the blind subjects, whereas it was shifted and located near the cyclopean eye for the sighted subjects. The results indicate that both early blind and sighted humans adequately transform the head-centered acoustic target coordinates into the required reference frame of either motor system, but that the adopted response strategy may be specific to the subject group and pointer method.

Adult↗

A comparison of neural computations underlying stereo vision and sound localization.

Stereo vision and sound localization are behaviors that help organisms to orient in space. Stereo vision provides information about the distance of an object. In sound localization mainly directional signals are analyzed. Two specific cues, binocular disparities underlying stereo vision, and the interaural time difference, suited to represent azimuth in sound localization, have many computational problems in common, although they are generated in two different modalities. The extraction of both cues requires a comparison of signals that arise from two independent sensors, called two-sensor comparison here. This two-sensor comparison is achieved by algorithms similar to summation, half-wave rectification and multiplication. Since the underlying neurons are band-pass filters, the two-sensor comparison results in ambiguities. These are removed in a hierarchical way in several computational steps, involving squaring, inhibition and across-frequency integration.

Animals↗

Effects of tectal grafts on sound localization deficits induced by inferior colliculus lesions in hooded rats.

The goals of this research were to examine the role of the inferior colliculus (IC) in mediating sound localization behavior and the ability of tectal grafts to restore function after IC ablation in the Long-Evans rat. Previous work has suggested that the IC is a major center for processing of information used in localizing sound sources in space. Adult rats were trained on a lick suppression paradigm to discriminate the location of the second pulse in a noise burst pair presented in the horizontal interaural plane. Following baseline testing, rats received bilateral IC lesions, bilateral lesions followed in 1 week by bilateral tectal grafts, or were sham operated. Sound localization ability was then tested 15 to 30 days and 40 to 50 days following surgical procedures. Performance across experimental groups was statistically the same during baseline testing. During the first operative test period lesion-only and grafted animals showed deficits in sound localization ability relative to controls. By the second postoperative test period control and grafted animals did not differ statistically in sound localization ability and performance of both groups was superior to that of lesion-only animals. Histology revealed a similar extent of IC damage in lesion-only and lesion-graft animals and revealed the presence of implanted tectal tissue in all grafted animals. There was significant neuron loss in the dorsal nucleus of lateral lemniscus (DNLL) in lesion-only animals relative to grafted rats and sham controls. Behavioral results suggest that the IC of pigmented rat is important for sound localization ability. The sparing of DNLL neurons in grafted animals suggests that the tectal grafts may directly integrate into or aid intrinsic recovery of the host auditory pathway.

Animals↗

Horizontal and vertical effects of eye-position on sound localization.

The effect of gaze direction on the localization of sound sources was investigated in the azimuthal and elevational dimension using a pointing task. In both dimensions, eccentric eye-position induced a significant shift in sound localization that was opposite to the direction of eccentricity. This finding is in accordance with the view that the azimuthal and elevational components of the auditory spatial information are processed in common neural substrates.

Acoustic Stimulation↗

Sound localization in newborn human infants.

Newborns' localization of sounds was examined in two experiments that utilized different psychophysical procedures and imposed different task demands. The results of both experiments were consistent in indicating that neonates not only differentiate the hemifield of a sound source but have some capacity to localize a sound within the hemifields. Adjustment of their initial head turn angle following a within-hemifield shift in location of an ongoing sound indicated that head orientation in neonates is elicited not only by sound onset but also by changes in location of an ongoing sound. Thus, multiple stimulus parameters impact on this neonatal response. Results are related to research on sound localization in older infants, and discussed in light of early development of the central auditory system.

Arousal↗

The effect of gaze direction on sound localization in brain-injured and normal adults.

This study examined the effects of eye position on sound localization in normal and brain lesion subjects. On the assumption that cerebral lesions may disrupt the representation of or attention to auditory space in the contralesional hemispace, we predicted that subjects with brain lesions would be less accurate in localizing sounds in the contralesional hemispace. In Experiment 1 we showed that gazing to the midline subjects with brain lesions were indeed impaired in localizing sounds in the contralesional hemispace. On the assumption that spatial attention is deployed at the site to which gaze is directed, we predicted that sound localization would be better on the side to which subjects directed their gaze. In Experiment 2, brain lesion subjects performed significantly better in the contralesional hemispace when they directed gaze to that hemispace. This improvement was accompanied by deterioration of performance in the ipsilesional hemispace. When subjects directed gaze to the ipsilesional hemispace, performance in the contralesional hemispace was further impaired. The effect of gaze was also observed in normal subjects in Experiments 2 and 3, independently of response mode (verbal versus pointing responses). These findings are consistent with the hypothesis that sound location may be mapped in eye-centered coordinates and that directing gaze to one hemispace reduces attentional allocation to the other hemispace.

Acoustic Stimulation↗

Sound localization: information theory analysis.

Sound localization has been studied extensively. Curiously, although much is known about factors that affect errors, little is known about factors that influence response time. Three experiments were performed in an attempt to identify the separate influence of each of several different factors. All trials used a single broadband noise signal emanating from one of a subset of six loudspeakers equally spaced around the participant in the azimuthal plane. Both the size of the subset and the balance of relative probabilities from speaker to speaker were altered to evaluate the relationship between information content and the dependent variable, choice reaction time. Choice reaction time was found to be related to the information content of the sound stimulus in all cases. It was also found to be related to the presence of pairs of speakers that were symmetrically opposed in front of the behind the participant. Models of choice reaction time in a sound localization task have clear implications for practice. For example, they suggest that multiple auditory collision warnings may endanger drivers.

Adult↗

Temporal weighting in sound localization.

The dynamics of sound localization were studied using a free-field direct localization task (pointing to sound sources) and an observer-weighting analysis that assessed the relative influence of each click in a click-train stimulus. In agreement with previous studies of the precedence effect and binaural adaptation, weighting functions showed increased influence of the onset click when the interclick interval (ICI) was short (<5 ms). For longer ICIs, all clicks in a train contributed roughly the same amount to listeners' localization responses. Finally, when a short gap was introduced in the middle of a train, the influence of the click immediately following the gap increased, in agreement with the "restarting" results obtained by Hafter and Buell [J. Acoust. Soc. Am. 88, 806-812 (1990)].

Acoustic Stimulation↗

Hearing in the elephant (Elephas maximus): absolute sensitivity, frequency discrimination, and sound localization.

A young Indian elephant was tested to determine its absolute sensitivity, frequency-discrimination thresholds, and sound-localization thresholds. The elephant was found to have an audibility curve similar to that of other mammals but one that is more sensitive to low frequencies and less sensitive to high frequencies than any other mammalian audiogram including human's. The elephant's sensitivity to frequency differences at low frequencies was found to equal that of humans. Finally, the elephant was found to be very accurate at localizing sounds in the azimuthal plane, with thresholds around 1 degree for broad-band noise. The elephant's ability to localize pure tones suggested that it could use both binaural time- and intensity-difference cues to localize sound.

Animals↗

Sound localization in an Old-World fruit bat (Rousettus aegyptiacus): acuity, use of binaural cues, and relationship to vision.

The passive sound-localization acuity of Egyptian fruit bats (Rousettus aegyptiacus) was determined using a conditioned-avoidance procedure. The mean minimum audible angle for left-right discrimination for 3 bats was 11.6 degrees--very near the mean for terrestrial mammals. The bats also were able to localize low- and high-frequency pure tones, indicating that they can use both binaural phase-difference and binaural intensity-difference cues to localize sound. Moreover, they were able to use the binaural phase-difference cue up to at least 5.6 kHz, which is higher than other mammals yet tested. The width of the Egyptian fruit bats' field of best vision was 27 degrees. This value is consistent with the hypothesis that the role of passive sound localization is to direct the eyes for visual scrutiny of sound sources. Thus, the passive localization abilities of these echolocating megachiropteran fruit bats do not deviate from the patterns established for nonecholocating mammals.

Animals↗

Sensitive and critical periods for visual calibration of sound localization by barn owls.

This study describes developmental changes in the capacity of owls to adjust sound localization in response to chronic prismatic displacement of the visual field and to recover accurate sound localization following the restoration of normal vision. Matched, binocular displacing prisms were mounted over the eyes of 19 barn owls (Tyto alba) beginning at ages ranging from 10 to 272 d. In nearly all cases, the visual field was shifted 23 degrees to the right. Sound localization was assessed on the basis of head orientations to sound sources, measured in a darkened sound chamber with a search coil system. Chronic exposure to a displaced visual field caused the owls to alter sound localization in the direction of the visual field displacement, thereby inducing a sound-localization error. The size of the sound-localization error that resulted depended on the age of the animal when prism experience began. Maximal errors of about 20 degrees were induced only when prism experience began by 21 d of age. As prism experience began at later ages, the magnitude of induced errors decreased. A bird that wore prisms beginning at 102 d of age, altered sound localization by only 6 degrees. An adult owl, when exposed chronically to a displaced visual field, altered sound localization by about 3 degrees. We refer to the early period in life when displaced vision induces exceptionally large sound-localization errors (relative to those induced in the adult) as a sensitive period. The capacity to recover accurate sound localization following restoration of normal vision was tested in 7 owls that had been raised wearing prisms. Four owls that had prisms removed by 182 d of age recovered accurate localization rapidly (over a period of weeks), whereas 3 owls that were older when the prisms were removed did not recover accurate localization when tested for up to 7 months after prism removal. Adjustment of sound localization slowed greatly or ceased at about 200 days of age, referred to here as the critical period for visual calibration of sound localization. Three owls were subjected repetitively to displacement of the visual field. An owl that adjusted sound localization to the left of normal during the sensitive period retained the capacity to adjust again to the left, but not to the right of normal, later in the critical period. The converse was true for an owl that adjusted sound localization to the right of normal during the sensitive period.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Physiological↗

Two-dimensional sound localization by human listeners.

This study measured the ability of subjects to localize broadband sound sources that varied in both horizontal and vertical location. Brief (150 ms) sounds were presented in a free field, and subjects reported the apparent stimulus location by turning to face the sound source; head orientation was measured electromagnetically. Localization of continuous sounds also was tested to estimate errors in the motor act of orienting with the head. Localization performance was excellent for brief sounds presented in front of the subject. The smallest errors, averaged across subjects, were about 2 degrees and 3.5 degrees in the horizontal and vertical dimensions, respectively. The sizes of errors increased, for more peripheral stimulus locations, to maxima of about 20 degrees. Localization performance was better in the horizontal than in the vertical dimension for stimuli located on or near the frontal midline, but the opposite was true for most stimuli located further peripheral. Front/back confusions occurred in 6% of trials; the characteristics of those responses suggest that subjects derived horizontal localization information principally from interaural difference cues. The generally high level of performance obtained with the head orientation technique argues for its utility in continuing studies of sound localization.

Adult↗

Quantitative analysis of sound localization with ocular positioning.

We studied the capacity for sound localization in the horizontal plane with measurement of the ocular position of the listener. The eye position responses elicited by tonal sound were asymmetrical in all six subjects and there was individual variation of frequency dependence. The sound pressure level and the angle of the loudspeaker also affected the accuracy of localization. Sound localization was more accurate, and individual variation lower, when the sound pressure level and the angle of the sound source were in the range 50 dBSL and 30 degrees, respectively. In the monoaural condition, the ear on the occluded side consistently showed displacement of responses toward the side of the non-occluded ear. Sound localization on the non-occluded side, however, showed various patterns of change in the monaural condition relative to the binaural condition. Cues as to the sound localization thus seem to differ with the side of the sound source.

Acoustic Stimulation↗

Comparison of relative and absolute sound localization ability in humans.

Sound localization ability has traditionally been studied using either a relative localization task, where thresholds to determine a difference in sound source location is approximately 1-10 degrees, or an absolute localization task, where the range of estimates of the source of a sound are 4-30 degrees. In order to directly relate these two psychophysical methods, we compared the psychometric functions from a relative localization task in a human subject to the same subject's performance on an absolute localization task using three different acoustic stimuli: Gaussian noise, 1-kHz tones, and 4-kHz tones. The results showed that the relative localization threshold was a poor indicator of the range of estimates of the same stimulus in absolute space, however, the width of the relative localization psychometric functions was well correlated with the width of the distribution of estimates made in the absolute localization task. It is concluded that the relative localization psychometric functions, but not threshold, provides a reliable estimate of absolute spatial localization ability in human subjects, and suggested that the same neuronal mechanisms can underlie the psychophysical data using both methods.

Adult↗