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[Sound localization in patients with asymmetrical hearing loss].

Good directional hearing ability demands good and symmetrical hearing in both ears. We report the effect of impaired hearing on the directional hearing ability of 98 patients, especially of patients with bilateral asymmetrical hearing loss. The directional testing device included 12 loudspeakers placed at 30 degree intervals in a circle with a diameter of 3.25 m, whose centre lay between the ears of the patient. In included an audiometer for producing the signals, an amplifier and a PDP11/23 computer interfaced to a loudspeaker switch bank. The subject's answers to 60 directionally randomized stimuli were recorded. During the presentation of the signal the patients were not allowed to turn their head. The patients had to name the number of the loudspeaker on the circle that they thought was producing the sound. In addition to the directional hearing test a pure-tone audiogram was done, and the middle- and high-frequency hearing loss estimated. The records of the directional hearing test were analysed in two new ways: firstly, vector analysis of the errors; secondly, averaging of the difference between the true interaural time delay and the virtual time difference, which was implicated in the possibly incorrect answer of the patient (effective delta-t-parameter). This average gives a score for the uncertainty in defining the correct "cone of confusion". In addition to the statistical analysis, two cases are reported showing the directional hearing ability of two patients with neuromas treated by transtemporal surgery, with some residual hearing.(ABSTRACT TRUNCATED AT 250 WORDS)

Audiometry↗

Single cortical neurons serve both echolocation and passive sound localization.

The pallid bat uses passive listening at low frequencies to detect and locate terrestrial prey and reserves its high-frequency echolocation for general orientation. While hunting, this bat must attend to both streams of information. These streams are processed through two parallel, functionally specialized pathways that are segregated at the level of the inferior colliculus. This report describes functionally bimodal neurons in auditory cortex that receive converging input from these two pathways. Each brain stem pathway imposes its own suite of response properties on these cortical neurons. Consequently, the neurons are bimodally tuned to low and high frequencies, and respond selectively to both noise transients used in prey detection, and downward frequency modulation (FM) sweeps used in echolocation. A novel finding is that the monaural and binaural response properties of these neurons can change as a function of the sound presented. The majority of neurons appeared binaurally inhibited when presented with noise but monaural or binaurally facilitated when presented with the echolocation pulse. Consequently, their spatial sensitivity will change, depending on whether the bat is engaged in echolocation or passive listening. These results demonstrate that the response properties of single cortical neurons can change with behavioral context and suggest that they are capable of supporting more than one behavior.

Animals↗

Sound localization, use of binaural cues and the superior olivary complex in pigs.

Noise localization thresholds and the ability to localize pure tones at 60 degrees separation were determined for three domestic pigs using a conditioned avoidance procedure. The average threshold for localizing a brief noise burst was 4.5 degrees which is much more accurate than the thresholds of other hoofed mammals, such as horses, cattle and goats. The ability of pigs to localize low-frequency tones indicates that they can use the binaural phase-difference cue. However, they were unable to localize tones of 4 kHz and higher, indicating that, like other hoofed mammals, their ability to use binaural intensity cues is greatly restricted if not completely absent. An examination of the superior olivary complex of pigs revealed that in relative size, shape and cell density it is more like that of cats than that of other hoofed mammals.

Animals↗

Pinna movements of the cat during sound localization.

We measured the movements of the external ear, or pinna, using the magnetic search coil technique in cats trained to look at auditory and visual targets for a food reward. No behavioral contingencies were placed on pinna movements. Prominent pinna movements accompany eye movements when the animal orients to either auditory or visual stimuli. In visual trials the pinna movements are coordinated with eye movements, suggesting that they are part of the general orientation response of the animal. In auditory trials the pinna response was composed of two movements: short- and long-latency components. Whereas the long-latency component seemed to occur with the eye movement to the target, the short-latency component was coupled to the onset of the stimulus. The short-latency component ( approximately 25 msec) was highly asymmetrical, being largest in the pinna ipsilateral to the stimuli. In one animal it persisted after >10(5) trials.

Acoustic Stimulation↗

Peripheral basis of sound localization in anurans. Acoustic properties of the frog's ear.

Directional responses of single auditory fibers in the eighth nerve of northern leopard frogs (Rana pipiens) were studied in order to gain some insights into the acoustical properties of the frog's ear. In addition to the actual directional response of a fiber, a theoretical directional-response curve to the intensity-rate function of the unit. The difference in the two responses provided a measure of the directional characteristics of the frog's ear at the stimulating frequency which can be plotted in a polar diagram to show the directivity pattern of the frog's acoustic receiver. Directivity patterns were obtained from three groups of experimental animals under the following conditions: (I) mouth filled with moistened cotton; (II) contralateral ear coated with silicone rubber cement; (III) open mouth. Changes in the directivity patterns were observed with experimental manipulations and these were compared to those obtained from normal animals (Feng, A.S. (1980) J. Acoust. Soc. AM. 68, 1107-1114). The results suggest that the frog's ear behaves as a combination pressure-pressure gradient receiver.

Animals↗

Earmuffs, exploratory head movements, and horizontal and vertical sound localization.

In a semi-anechoic room, normal-hearing adults judged the position of that loudspeaker emitting a narrow-band noise centered at 1 kc/s, from a vertical array of 10 loudspeakers in 18 degrees steps, or a similar horizontal-arc array intersecting at 0 degrees azimuth and 0 degrees vertical. Stimuli were narrow-band noise bursts terminated by S when judgment was made. Ss (N:17) were free to move their heads, or were asked to restrict such movement. In the horizontal plane, Ss without earmuffs and with free head movement performed with 95% absolute accuracy but, with earmuffs, accuracy fell off to 50%, and when head movements were restricted accuracy fell off further to 24%. The results of Fisher and Freeman (J. Aud. Res., 1968, 8, 15-26) were generally confirmed, but free head movements did not, as in their study, totally "wash out" functional pinna removal. In the vertical plane, Ss with earmuffs even with free head movements yielded only 19% absolute accuracy, though without earmuffs accuracy rose to 72%. A postulate arising from this study is that listeners are unable to recruit remaining (interaural) cues when these are generated under different bodily orientations. The potential practical hazard suggested by the results is noted.

Auditory Perception↗

The auditory periphery of the ferret. II: The spectral transformations of the external ear and their implications for sound localization.

In the previous paper the directional response characteristics of the ferret auditory periphery were examined. In this study further measurements of the spectral transfer functions (STFs) of the auditory periphery were obtained at locations close to the tympanic membrane. There was considerable variation in the STFs recorded from different animals and between recordings made at each end of the auditory canal in the same animal. However, calculation of the so called "location dependency function" demonstrated that changes in the location of the stimulus produced the same pattern of changes in the STFs in all recordings. Changes in the spectral transformation for azimuth locations in the ipsilateral auditory field were examined by calculating the horizon STF. The gain transformations of frequencies below 20 kHz were found to be asymmetrical about the interaural axis so that maximum gain was obtained for anterior stimulus locations. In contrast, the maximum gain for frequencies above 20 kHz was obtained for stimulus locations about the interaural axis, and movement of the stimulus location into either the anterior or posterior fields produced symmetrical reductions in gain. These changes were related to the directional properties of the periphery examined in the previous paper [S. Carlile, J. Acoust. Soc. Am. 88, 2180-2195 (1990)]. The spatial resolution of the monaural information provided by the peripheral STFs is dependent on the rate of change of the transformations as a function of azimuthal displacement of the stimulus location. This was examined by calculating the unsigned first spatial derivative for each frequency in the horizon STF.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Vision-independent adjustment of unit tuning to sound localization cues in response to monaural occlusion in developing owl optic tectum.

Neurons in the developing optic tectum adjust their tuning to auditory localization cues in response to chronic monaural occlusion so that auditory spatial fields align with visual receptive fields (VRFs). We tested whether this adaptive adjustment of auditory tuning requires visual instruction. Both eyelids were sutured closed at the same time that one ear was occluded in two barn owls that were 1 month old. After 70 and 100 d, respectively, the tuning of units to interaural level difference (ILD) and to interaural time difference (ITD) was measured. These data were compared with equivalent data from 15 normal owls. Unit tuning to ITD was shifted from normal in both of the monaurally occluded owls. In one owl, ILD tuning was also clearly shifted. In the other owl, the map of ILD was flipped upside down and adaptive adjustments in ILD tuning could not be assessed. Instead, adjustments in ILD tuning were observed following removal of the earplug with the eyelids kept closed. Unit tuning was monitored at several sites in the tectum for 1 month after earplug removal using chronically implanted electrodes. Then, ILD tuning was resampled across the entire tectum. Both measures indicated shifts in ILD tuning in response to removal of the earplug in the second blind owl. In both animals, the magnitude of the shifts in ILD tuning and ITD tuning was smaller than has been observed previously in monaurally occluded but sighted owls. The results demonstrate that the brain can make adaptive adjustments in ILD and ITD tuning in response to early monaural occlusion even without the guiding influence of vision.

Adaptation, Physiological↗

Sound localization in chinchillas, III: Effect of pinna removal.

The ability of chinchillas to make left/right, front/back, and vertical locus discriminations was determined before and after surgical removal of the pinnae. The animals were tested behaviorally using a conditioned avoidance procedure. In the left/right localization tests, removal of both pinnae had no effect on localization acuity for broadband noise but did result in a small decrement in performance when localizing low-pass filtered noise. In the front/back localization tests, removal of a single pinna resulted in a small but consistent decrement in performance when the sound sources were located in the hemifield on the same side as the intact pinna, and a greater decrement when the sound sources were located in the hemifield on the side of the missing pinna; removal of both pinnae resulted in the largest decrement in performance. Finally, vertical localization acuity and performance when localizing low-pass filtered noise were greatly impaired following removal of both pinnae. These results demonstrate the importance of the pinnae in performing front/back and vertical localization tasks in which binaural cues are not available.

Acoustic Stimulation↗

Effects on sound localization of configuration and type of hearing impairment.

Localization ability of 87 bilaterally hearing-impaired listeners was tested in the horizontal and vertical planes, frontally and laterally. In those with sensorineural hearing loss, it was found that deficits in localization accuracy in different regions of auditory space could be related to different configurations of hearing loss. For example, there were associations between vertical plane discrimination and high-frequency sensitivity; and front-rear discrimination and mid-to-high-frequency sensitivity. These results agree with theoretical expectations, while the outcome overall contrasts with previous reports that localization performance is unrelated to audiometric configuration. A comparison of 13 listeners with conductive/mixed types of impairment with a sensorineural-loss group, matched for degree of loss, showed that a conductive component adds significantly to localization disturbance, particularly in the horizontal plane. The probable reason is a disturbance of low-frequency interaural time cues, and this occurs because a higher proportion of low-frequency sound is likely to be transmitted via bone conduction relative to air conduction. Correlations between hearing loss and localization are only moderate, suggesting that aspects of hearing impairment, in addition to simple attenuation, may also reduce auditory localization performance.

Adult↗