[Localization of sound stimulus, role of spatio-energetic parameters].
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CONCLUSION: The findings of this study suggest that acoustic spatial perception during head movement is achieved by the vestibular system, which is responsible for the correct dynamic of acoustic target pursuit. OBJECTIVE: The ability to localize sounds in space during whole-body rotation relies on the auditory localization system, which recognizes the position of sound in a head-related frame, and on the sensory systems, namely the vestibular system, which perceive head and body movement. The aim of this study was to analyse the contribution of head motion cues to the spatial representation of acoustic targets in humans. MATERIAL AND METHODS: Healthy subjects standing on a rotating platform in the dark were asked to pursue with a laser pointer an acoustic target which was horizontally rotated while the body was kept stationary or maintained stationary while the whole body was rotated. The contribution of head motion to the spatial acoustic representation could be inferred by comparing the gains and phases of the pursuit in the two experimental conditions when the frequency was varied. RESULTS: During acoustic target rotation there was a reduction in the gain and an increase in the phase lag, while during whole-body rotations the gain tended to increase and the phase remained constant. The different contributions of the vestibular and acoustic systems were confirmed by analysing the acoustic pursuit during asymmetric body rotation. In this particular condition, in which self-motion perception gradually diminished, an increasing delay in target pursuit was observed.
By Fourier's theorem, signals can be decomposed into a sum of sinusoids of different frequencies. This is especially relevant for hearing, because the inner ear performs a form of mechanical Fourier transform by mapping frequencies along the length of the cochlear partition. An alternative signal decomposition, originated by Hilbert, is to factor a signal into the product of a slowly varying envelope and a rapidly varying fine time structure. Neurons in the auditory brainstem sensitive to these features have been found in mammalian physiological studies. To investigate the relative perceptual importance of envelope and fine structure, we synthesized stimuli that we call 'auditory chimaeras', which have the envelope of one sound and the fine structure of another. Here we show that the envelope is most important for speech reception, and the fine structure is most important for pitch perception and sound localization. When the two features are in conflict, the sound of speech is heard at a location determined by the fine structure, but the words are identified according to the envelope. This finding reveals a possible acoustic basis for the hypothesized 'what' and 'where' pathways in the auditory cortex.
The effect of uni- and bilateral denervation of muscles of the pinna on the audio-visual targeting reflex reinforced by food was studied. In comparison with the normal group the unilaterally denervated animals showed a decreased capacity to localize sound sources placed behind the animal ipsi- and contralaterally to the operated side. The denervation of the second ear in these animals induced a further decrease of the localization scores, especially of the sources placed behind them. The localization behavior strategies were different depending on the integrity of the innervation of muscles of the pinna. The stimulation of the operated side with tones of a 30 dB higher intensity than in the normal side did not improve the animalsperformance in localizing the sound sources. The shortening of duration from 500 to 50 ms reduced, the capacity to localize the loudspeakers placed ipsilaterally to the denervated side, especially those behind the animal. The role for the targeting reflex of the feedback information from the muscles controlling the pinna movements, and the significance of the postural changes induced by the tone are discussed.
The precedence effect (PE) describes several spatial perceptual phenomena that occur when similar sounds are presented from two different locations and separated by a delay. The mechanisms that produce the effect are thought to be responsible for the ability to localize sounds in reverberant environments. Although the physiological bases for the PE have been studied, little is known about how these sounds are localized by species other than humans. Here we used the search coil technique to measure the eye positions of cats trained to saccade to the apparent locations of sounds. To study the PE, brief broadband stimuli were presented from two locations, with a delay between their onsets; the delayed sound meant to simulate a single reflection. Although the cats accurately localized single sources, the apparent locations of the paired sources depended on the delay. First, the cats exhibited summing localization, the perception of a "phantom" sound located between the sources, for delays < +/-400 micros for sources positioned in azimuth along the horizontal plane, but not for sources positioned in elevation along the sagittal plane. Second, consistent with localization dominance, for delays from 400 micros to about 10 ms, the cats oriented toward the leading source location only, with little influence of the lagging source, both for horizontally and vertically placed sources. Finally, the echo threshold was reached for delays >10 ms, where the cats first began to orient to the lagging source on some trials. These data reveal that cats experience the PE phenomena similarly to humans.
Four experiments explored possible roles for working memory in sound localization. In each experiment, the angular error of localization was assessed when performed alone, or concurrently with a working-memory task. The role of the phonological slave systems in auditory localization was ruled out by Experiments 1 and 2, while an engagement of central resources was suggested by the results of Experiment 3. Experiment 4 examined the involvement of visuo-spatial systems in auditory localization and revealed impairment of localization by the concurrent spatial working-memory task. A comparison of dual-task decrement across all four studies suggests that localization places greater demand on central than on spatial resources.
We have used positron emission tomography (PET) to measure regional cerebral blood flow (rCBF) in sighted and congenitally blind subjects performing auditory localization tasks. During scanning, the spectral and binaural cues of localized sound were reproduced by a sound system and delivered via headphones. During tasks that required auditory localization both the sighted and blind subjects strongly activated posterior parietal areas. In addition, the blind subjects activated association areas in the right occipital cortex, the foci of which were similar to areas previously identified in visual location and motion detection experiments in sighted subjects. The blind subjects, therefore, demonstrated visual to auditory cross-modal plasticity with auditory localization activating occipital association areas originally intended for dorsal-stream visual processing. To determine the functional connectivity of pre-selected brain regions in primary and non-primary auditory and posterior parietal cortex in the two cohorts, we performed an inter-regional correlation analysis on the rCBF data set. During auditory localization in the blind subjects, rCBF activity in the right posterior parietal cortex was positively correlated with that in the right occipital region, whereas in sighted subjects correlations were generally negative. There were no significant positive occipital correlations in either cohort when reference regions in temporal or left parietal cortex were chosen. This indicates that in congenitally blind subjects the right occipital cortex participates in a functional network for auditory localization and that occipital activity is more likely to arise from connections with posterior parietal cortex.
Sound localization can be affected by vision; in the ventriloquism effect, sounds that are hard to localize within hearing become mislocalized toward the location of concurrent visual events. Here we tested whether spatial attention is drawn to the illusory location of a ventriloquized sound. The study exploited our previous finding that visual cues do not attract auditory attention. We report an important exception to this rule; auditory attention can be drawn to the location of a visual cue when it is paired with a concurrent unlocalizable sound, to produce ventriloquism. This demonstrates that crossmodal integration can precede reflexive shifts of attention, with such shifts taking place toward the crossmodally determined illusory location of a sound. It also shows that ventriloquism arises automatically, with objective as well as subjective consequences.
Many studies have been conducted to measure monaural azimuthal sound localization performance with different sounds varying in frequency and complexity, but few have used linguistic stimuli. The present experimental design used subjects' first names in a monaural azimuthal localization task. Analysis of response accuracy showed that subjects are not more accurate in localizing their own first name than in localizing other first names and that there was no significant advantage of one ear over another. Reaction times were shorter when the subjects localized their own first name than when they localized any other first names and there was no significant ear advantage, but localizing other first names took more time with the right than with the left ear. All stimuli were better and more quickly localized on the side of the open ear, and there was no difference in acuity or velocity of localization with the two different speaker voices used. These results suggest that first names are processed through the controlateral auditory pathway and can be analyzed in the right hemisphere.
Acquisition of a sound localization discrimination by rats was investigated. Two loudspeakers were located outside an experimental enclosure containing two levers and a dipper feeder. In the same-side condition, responses on the lever nearest the sound-producing speaker were reinforced. Animals in this condition acquired the discrimination rapidly, generally within the first session. In the opposite-side condition, responses on the lever furthest from the sound-producing speaker were reinforced. Acquisition for animals in this condition began below the chance level (50% correct responses) and took on the order of 10 sessions to approach the final, high level. The course of acquisition in both cases appeared to depend upon an initial tendency of rats to respond on the lever nearest the source of sound in this situation. The rise-decay time of the 4-kHz tone burst signal clearly affected the performance level reached. It did not, however, affect the rate at which the discrimination was acquired.
Infants aged 2 and 6 months were tested with the precedence effect, an auditory phenomenon involving sound localization. Each infant was tested with two types of stimuli: sound from a single loudspeaker and precedence-effect sounds produced by the same sound put through two loudspeakers, with one output leading the other by 7 msec. Older infants localized precedence-effect stimuli as they did single-source stimuli, indicating that they perceived this phenomenon as expected. Two-month-olds turned their heads toward single-source sounds, but did not localize precedence-effect sounds, suggesting that that more difficult perceptual task had not been achieved at this age. In general, head-turning toward sound proved far more difficult to elicit in younger infants. A click train was ineffective, but a tape-recorded human voice elicited above-chance low-level turning. The developmental changes in auditory behavior are discussed in terms of the rapid growth of the auditory cortex.
The precedence effect is an auditory illusion produced by presenting the same signal through 2 loudspeakers, with 1 leading the other by several milliseconds. Adults perceive a sound localized exclusively on the leading side and directionally equivalent to a single source sound. Because the precedence effect is thought to involve cortical functions, newborns were expected not to respond with directional head turning toward these sounds. Newborns were presented with a tape-recorded rattle sound produced in 3 ways: through a single loudspeaker located right or left, through both loudspeakers with 1 onset leading the other by 7 msec, and control stimuli in which both loudspeakers sounded simultaneously, resulting in an apparent center location of the sound. Newborns turned toward the single source sound, but neither to precedence effect stimuli nor control stimuli. These results were related to maturation of the auditory cortex.
Interaural time differences (ITDs) are a major cue for localizing the azimuthal position of sounds. The dominant models for processing ITDs are based on the Jeffress model and predict neurons that fire maximally at a common ITD across their responsive frequency range. Such neurons are indeed found in the binaural pathways and are referred to as "peak-type." However, other neurons discharge minimally at a common ITD (trough-type), and others do not display a common ITD at the maxima or minima (intermediate-type). From recordings of neurons in the auditory cortex of the unanesthetized rabbit to low-frequency tones and envelopes of high-frequency sounds, we show that the different response types combine to form a continuous axis of best ITD. This axis extends to ITDs well beyond that allowed by the head width. In Jeffress-type models, sensitivity to large ITDs would require neural delay lines with large differences in path lengths between the two ears. Our results suggest instead that sensitivity to large ITDs is created with short delay lines, using neurons that display intermediate- and trough-type responses. We demonstrate that a neuron's best ITD can be predicted from (1) its characteristic delay, a rough measure of the delay line, (2) its characteristic phase, which defines the response type, and (3) its best frequency for ITD sensitivity. The intermediate- and trough-type neurons that have large best ITDs are predicted to be most active when sounds at the two ears are decorrelated and may transmit information about auditory space other than sound localization.