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Changes in frequency spectra of breath sounds during histamine challenge test in adult asthmatics and healthy control subjects.

Air-flow standardized breath sounds were recorded at the chest and at the trachea during histamine challenge test and after subsequent bronchodilation in 12 asthmatics and 6 healthy controls for spectral analysis, to be compared with simultaneous changes in spirometric variables. Of all the lung sound variables measured, the changes in median frequency of the power spectrum (F50) of tracheal expiratory sounds were found to correlate best (r = 0.853, p < 0.0001) with changes in FEV1. The increase of F50 during histamine challenge was significantly larger in asthmatics than in healthy control subjects (p < 0.005). The provocative dose of histamine inducing a decrease of 15 percent in FEV1 (PD15FEV1) and the provocative dose causing an increase of 30 percent in tracheal expiratory F50 (PD30F50) were significantly related (r = 0.754, p = 0.012). In asthmatics, the breath sound frequency distribution in terms of median frequency reflected acute changes in airways obstruction with high sensitivity and specificity. The present method for breath sound analysis can be applied for patients with limited cooperation during bronchial challenge tests.

Adolescent↗

Decreased 3D-sound spatialization accuracy caused by speech bandwidth limitation over commodity audio components.

This paper studies the accuracy achievable in spatialized speech signals due to their limited bandwidth, in systems based on generic Head-Related Transfer Functions (HRTFs). The accuracy in the perception of sounds spatialized through HRTFs to emulate nine sound locations around the listener, at 0 elevation, are investigated. The tests contrast the localization accuracy for a speech segment and that for broadband noise, as perceived by two independent groups of 10 normal-hearing volunteers each. The sound localization perceived and reported by each subject is compared to the HRTF-emulated location, to define a localization error, in each case. The results are analyzed through a repeated measures, mixed-factorial design Analysis of Variance (ANOVA). The emulated source locations and the type of sounds are the independent variables, and the average perceived localization error for each case, the dependent variable. Since the spectrum of speech signals drive only sections of the complete HRTF frequency response for each location, the initial expectation is that they benefit less from the spectral-shaping process implemented by the HRTFs, thus resulting in a lower spatialization efficiency than the one for a full-spectrum noise signal. We study the measurement of these effects when 3D-sounds are delivered over commodity audio components, because of their widespread use in practical systems.

Adult↗

Physiologic chest sounds and helicopter engine noise.

To develop an amplification system for physiologic chest sounds during air medical transport in jet helicopters, we compared frequency spectra of physiologic chest sounds and Allison C-28 equipped jet helicopter noise. We found that the frequency spectrum of physiologic chest sounds is contained entirely within that of jet rotocraft noise. Attempts to amplify physiologic chest sounds or to filter jet rotorcraft noise will invariably fail to improve perception of chest sounds. Future research must focus on assessment of actual movement of the chest and of each hemithorax, as well as an carbon dioxide production, as indicators of adequate ventilation and proper endotracheal tube position.

Air Ambulances↗

Auditory-visual synesthesia: sound-induced photisms.

Nine patients with visual loss due to lesions of the optic nerve or chiasm experienced photisms induced by sound. Descriptions of these varied from simple flashes of white light to complicated colorful hallucinations likened to a flame, a petal of oscillating lines, a kaleidoscope, or an ameba; they always appeared within a defective portion of the visual field as demonstrated by perimetry. The provoking sounds were usually those of normal daily life, ranged from soft to loud, and always seemed to be heard by the ear ipsilateral to the eye in which the photism was seen. Sound-induced photisms occurred under circumstances that would promote a startle reaction to sound, and each patient was startled when the photisms occurred. Visual evoked responses demonstrated partial deafferentation of the eye in which photisms were seen in seven patients tested. The phenomenon may occur when the patient with a partially deafferent anterior visual pathway is startled by sound.

Adult↗

Recording sound from human skeletal muscle: technical and physiological aspects.

In order to examine technical factors that influence muscle sound recording, single twitches of muscle were utilized since their waveforms were likely to be reproducible. We observed that satisfactory recordings could be made with either Archer air interface, or Hewlett-Packard direct contact sensor, microphones. Firm contact and stability between the microphone and the skin surface were particularly important. Frequencies below 20 Hz, the lower limit of the human auditory range, must be recorded, since they account for at least 90% of the power of the muscle sound wave. The chief frequencies were below 4 Hz. The sound wave produced by a maximal twitch of human thenar muscle induced by median nerve stimulation at the wrist is maximal in amplitude over the center and recedes to near zero at the margins of the muscle. It is preceded by the muscle compound action potential and is followed by the force curve, recorded with a strain gauge attached to the thumb. The sound resembles force in total time course, and it increases with increasing strengths of nerve stimulation. However, it differs in its latency, phase relationships, and response to nerve stimulation at different frequencies. Some of the features of muscle sound suggest it relates to both the active contractile and the parallel elastic components of muscle during a twitch contraction, but not the series elastic component.

Adult↗

Comparison of the lung sound frequency spectra of infants and adults.

Auscultation of the infant chest reveals lung sounds that seem different from those of adults. To characterize this subjective difference, we compared the phonopneumographic median frequencies of lung sounds of seven full-term and six premature infants with those of seven adults free of cardiopulmonary disease. The median frequencies over the upper lobes for the adults, term infants, and premature infants were 282 +/- 63(SD) Hz, 383 +/- 80 Hz, and 483 +/- 86 Hz, respectively. At this location the differences among the three groups were significant (p less than 0.01). Over the lower lobes, the median frequencies for the adults, term infants, and premature infants were 243 +/- 56 Hz, 386 +/- 76 Hz, and 390 +/- 63 Hz, respectively. Here the difference between the adults and both groups of infants was significant (p less than 0.01), but that between the term and premature infants was not. We conclude that the normal lung sounds of newborn infants contain higher-frequency components than those of adults. We postulate that this difference is the result of less filtering of the lung sound in infants. This difference should be considered when lung sounds of infants are described or assessed for the presence of abnormalities.

Adult↗

Lung sounds in neonates with and without an added dead space.

Previous studies have reported great difficulty in recording lung sounds from neonates and have found conflicting results. We studied lung sounds in neonates during the inspiratory phase of the respiratory cycle as monitored by inductive plethysmography (A) and by a pneumotachograph and a face mask (B) which added a dead space of 12 mL. Sixteen term babies were tested 12 hr to 6 days (median 45 hours) after birth. Lung sounds were recorded and then analysed using overlapping and non-overlapping fast Fourier transforms. The two methods of analysis showed a difference in intensity but not in frequency. Fourteen babies provided enough breaths for comparison; a total of 596 inspirations were analysed. The intensity of lung sounds on occasion B was higher in all but two babies with a mean B/A ratio of 2.4. The mean (SD) power on occasions A and B was 13.9 (8.5) mW and 26.9 (21.0) mW, P = 0.02, respectively. In all but 4 babies the B/A ratios of the median (f50) and 90th centile (f90) frequencies were scattered randomly within 20% of unity. The mean (SD) f50 on occasions A and B was 205.5 (51.1) Hz and 225.8 (32.3) Hz, P = 0.10, respectively; the mean f90 was 370.3 (91.0) Hz and 396.1 (67.8) Hz, P = 0.25, respectively. Linear regression showed that there is a third-order polynomial relationship between sound intensity and air flow at the mouth. A weaker positive association exists between frequency and air flow, showing that the median and 90th centile frequencies approach an asymptote as flow increases.(ABSTRACT TRUNCATED AT 250 WORDS)

Auscultation↗

Azimuthal sound localization in the European starling (Sturnus vulgaris): I. Physical binaural cues.

The physical measurements reported here test whether the European starling (Sturnus vulgaris) evaluates the azimuth direction of a sound source with a peripheral auditory system composed of two acoustically coupled pressure-difference receivers (1) or of two decoupled pressure receivers (2). A directional pattern of sound intensity in the free-field was measured at the entrance of the auditory meatus using a probe microphone, and at the tympanum using laser vibrometry. The maximum differences in the sound-pressure level measured with the microphone between various speaker positions and the frontal speaker position were 2.4 dB at 1 and 2 kHz, 7.3 dB at 4 kHz, 9.2 dB at 6 kHz, and 10.9 dB at 8 kHz. The directional amplitude pattern measured by laser vibrometry did not differ from that measured with the microphone. Neither did the directional pattern of travel times to the ear. Measurements of the amplitude and phase transfer function of the starling's interaural pathway using a closed sound system were in accord with the results of the free-field measurements. In conclusion, although some sound transmission via the interaural canal occurred, the present experiments support the hypothesis 2 above that the starling's peripheral auditory system is best described as consisting of two functionally decoupled pressure receivers.

Acoustic Stimulation↗

Inheritance of male courtship sound characteristics in Drosophila littoralis.

Males of Drosophila littoralis vibrate their wings during courtship to deliver a "love song." This consists of 25- to 50-ms-long pulses with a basic frequency of about 250-400 Hz, separated by 250- to 500-ms pauses. When recording the sounds of flies from several localities in Europe, we found that males of one strain from northern Finland displayed courtship sounds with an unusually low wing beat frequency (below 250 Hz). In a genetic analysis utilizing marker stocks, the anomalous frequency was found to be caused by genes on all major autosomes, the strongest factors being on the second chromosome. Interaction between genes on chromosome 2 and on the fused chromosome 3-4 was non-additive. In low-frequency sounds, the number of cycles in the pulse (CN) was decreased, so that the length of the sound pulse (PL) remained more or less unchanged. We suggest that the genetically and physiologically most thoroughly controlled trait in the sound of Drosophila littoralis is the length of the pulse.

Animals↗

Automatic detection of sounds and murmurs in patients with Ionescu-Shiley aortic bioprostheses.

The problems encountered in the automatic detection of cardiac sounds and murmurs are numerous. The phonocardiogram (PCG) is a complex signal produced by deterministic events such as the opening and closing of the heart valves, and by random phenomena such as blood-flow turbulence. In addition, background noise and the dependence of the PCG on the recording sites render automatic detection a difficult task. In the paper we present an iterative automatic detection algorithm based on the a priori knowledge of spectral and temporal characteristics of the first and second heart sounds, the valve opening clicks, and the systolic and diastolic murmurs. The algorithm uses estimates of the PCG envelope and noise level to identify iteratively the position and duration of the significant acoustic events contained in the PCG. The results indicate that it is particularly effective in detecting the second heart sound and the aortic component of the second heart sound in patients with Ionescu-Shiley aortic valve bioprostheses. It has also some potential for the detection of the first heart sound, the systolic murmur and the diastolic murmur.

Algorithms↗

Binaural weighting of pinna cues in human sound localization.

Human sound localization relies on binaural difference cues for sound-source azimuth and pinna-related spectral shape cues for sound elevation. Although the interaural timing and level difference cues are weighted to produce a percept of sound azimuth, much less is known about binaural mechanisms underlying elevation perception. This problem is particularly interesting for the frontal hemifield, where binaural inputs are of comparable strength. In this paper, localization experiments are described in which hearing for each ear was either normal, or spectrally disrupted by a mold fitted to the external ear. Head-fixed saccadic eye movements were used as a rapid and accurate indicator of perceived sound direction in azimuth and elevation. In the control condition (both ears free) azimuth and elevation components of saccadic responses were well described by a linear regression line for the entire measured range. For unilateral mold conditions, the azimuth response components did not differ from controls. The influence of the mold on elevation responses was largest on the ipsilateral side, and declined systematically with azimuth towards the side of the free ear. Near the midsagittal plane the elevation responses were clearly affected by the mold, suggesting a systematic binaural interaction in the neural computation of perceived elevation that straddles the midline. A quantitative comparison of responses from the unilateral mold, the bilateral mold and control condition provided evidence that the fusion process can be described by binaural weighted averaging. Two different conceptual schemes are discussed that could underlie the observed responses.

Acoustic Stimulation↗

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↗

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↗

Diversity in sound pressure levels and estimated active space of resident killer whale vocalizations.

Signal source intensity and detection range, which integrates source intensity with propagation loss, background noise and receiver hearing abilities, are important characteristics of communication signals. Apparent source levels were calculated for 819 pulsed calls and 24 whistles produced by free-ranging resident killer whales by triangulating the angles-of-arrival of sounds on two beamforming arrays towed in series. Levels in the 1-20 kHz band ranged from 131 to 168 dB re 1 microPa at 1 m, with differences in the means of different sound classes (whistles: 140.2+/-4.1 dB; variable calls: 146.6+/-6.6 dB; stereotyped calls: 152.6+/-5.9 dB), and among stereotyped call types. Repertoire diversity carried through to estimates of active space, with "long-range" stereotyped calls all containing overlapping, independently-modulated high-frequency components (mean estimated active space of 10-16 km in sea state zero) and "short-range" sounds (5-9 km) included all stereotyped calls without a high-frequency component, whistles, and variable calls. Short-range sounds are reported to be more common during social and resting behaviors, while long-range stereotyped calls predominate in dispersed travel and foraging behaviors. These results suggest that variability in sound pressure levels may reflect diverse social and ecological functions of the acoustic repertoire of killer whales.

Animals↗

Effects of a sound source moving in a vertical plane on postural responses in humans.

The effects of moving sound sources on postural responses were studied. Sound source movement was simulated by sequential switching of loudspeakers located along an arch positioned in the sagittal plane relative to the subject. The total durations of the sound stimulus movement were 1.6, 3.2, and 4.8 sec. Signals of 1.6 and 3.2 sec led to decreases in the mean amplitude of oscillogram oscillations in the sagittal and frontal planes. Stabilogram curves averaged for all subjects for the signal of duration 4.8 sec showed that the center of gravity deviated during exposure to the sound stimulus towards the side opposite the direction of movement of the sound source.

Acoustic Stimulation↗

Aortic valve closure and cardiac vibrations in the genesis of the second heart sound.

Simultaneous M-mode echocardiograms and external phonocardiograms were recorded in 15 healthy subjects to evaluate the genesis of the second heart sound. The onset of the second sound was found synchronous with the coaptation of the aortic valve cusps and a sharp vibration on the aortic wall. The closed valve was oscillating for 30 to 45 ms after the coaptation of the cusps. Magnified echocardiographic studies of the interventricular septum revealed a consistent, momentary quiver across the septal myocardium a mean of 4 ms after the onset of the second sound. In most subjects, a transient myocardial vibration was observed in temporal association with the first heart sound as well. The present observations suggest that the aortic valve closure initiates the production of the second heart sound, the main audible component resulting, however, from vibrations in the cardiac structures after the valve closure.

Adult↗

Effects of vibration frequency and tissue thickness on intrauterine sound levels in sheep.

Pure-tone sinusoidal mechanical vibratory stimuli ranging in frequency from 4 to 4000 Hz were applied to the ventral abdominal wall of pregnant ewes, and intrauterine sound pressure levels were recorded with a hydrophone 5, 10, 15, and 20 cm from the surface. There were significant decreases in sound pressure levels with increasing frequencies (p less than 0.0001) and increasing depth (p = 0.01). There was no significant interaction between these two variables. An electronic artificial larynx was also activated on the abdominal wall, resulting in quite high sound pressure levels (mean, 119 dB) measured 5 cm from the surface, with a significant decrease in sound pressure levels as the thickness of the intervening maternal tissues increased (p = 0.005). These results suggest that the frequency of vibratory stimulus used and the thickness of the maternal abdominal wall could influence fetal response to the vibroacoustic stimulation test by affecting intrauterine sound pressure levels.

Acoustic Stimulation↗

A reversible method for sound analysis adapted to bio-acoustical experiments.

The paper describes a method of sound analysis, 'modulation analysis', its implementation on a minicomputer PDP12 and some aspects of its application in bioacoustical experiments. Modulation analysis reversibly resolves a given sound signal into time-courses of amplitude and carrier frequency. Since time is preserved as the independent variable the method provides a suitable basis for the computer modification of sounds. Problems of practical performance are discussed with regard to sounds of birds and insects. Further, the use of sound modification in a neurophysiological study of the hearing system of birds is described.

Animals↗