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At least 1,117 records · Page 62Linked to original sources
PubMed1999

An acoustical study of sound production in biphonic singing, Xöömij.

A theory that the high melody pitch of biphonic singing, Xöömij, is produced by the pipe resonance of the rear cavity in the vocal tract is proposed. The front cavity resonance is not critical to the production of the melody pitch. This theory is derived from acoustic investigations on several three-dimensional shapes of a Xöömij singer's vocal tract measured by magnetic resonance imaging. Four different shapes of the vocal tract are examined, with which the melody pitches of F6, G6, A6, and C7 are sung, along with the F3 drone of a specific pressed voice. The second formant frequency calculated from each tract shape is close to the melody pitch within an error of 36 cents. Sounds are synthesized by convolving a glottal source waveform provided by the Rosenberg model with transfer functions calculated from the vocal tract shapes. Two pitches are found to be successfully perceived when the synthesized sounds are listened to. In a frequency range below 2 kHz, their spectra have a strong resemblance to those of the sounds actually sung. The synthesized sounds, however, fail to replicate the harmonic clustering at 4-5 kHz observed in the actual sounds. This is speculated to originate from the glottal source specific to the "pressed" timbre of the drone.

Humans↗
PubMed2000

Frequency characteristics of sound transmission in middle ears from Norwegian cattle, and the effect of static pressure differences across the tympanic membrane and the footplate.

For 23 cadaver ears from Norwegian cattle, frequency characteristics for the round-window volume displacement relative to the sound pressure at the eardrum have been measured, and are compared to earlier results for human ears [M. Kringlebotn and T. Gundersen, J. Acoust. Soc. Am. 77(1), 159-164 (1985)]. For human as well as for cattle ears, mean amplitude curves have peaks at about 0.7 kHz. At lower frequencies, the mean amplitude for cattle ears is about 5 dB smaller than for human ears. The amplitude curves cross at about 2 kHz, and toward higher frequencies the amplitude for cattle ears becomes increasingly larger. If amplitude curves are roughly approximated by straight lines above 1 kHz, the slope for cattle ears is about -5 dB/octave as compared to about -15 dB/octave for human ears. The phase of the round-window volume displacement lags behind the phase of the sound pressure at the tympanic membrane. The phase lag is close to zero below 0.2 kHz, but increases to about 3.5 pi at 20 kHz for cattle ears, as compared to less than 2 pi for human ears. Further investigations are needed in order to explain the observed differences. Sound transmission in the ear decreases with an increasing static pressure difference across the tympanic membrane, especially at frequencies below 1 kHz, where pressure differences of 10 and 60 cm water cause mean transmission losses of about 10 and 26 dB, respectively, the losses being somewhat larger for overpressures than for underpressures in the ear canal. At higher frequencies, the transmission losses are smaller. For small overpressures, and in a limited frequency range near 3 kHz, even some transmission enhancement may occur. Static pressure variations in the inner ear have only a minor influence on sound transmission. Static pressures relative to the middle ear in the range 0-60 cm water cause mean sound transmission losses less than 5 dB below 1 kHz, and negligible losses at higher frequencies.

Animals↗
PubMed2000

The impact of sound speed errors on medical ultrasound imaging.

The results of a quantitative study of the impact of sound speed errors on the spatial resolution and amplitude sensitivity of a commercial medical ultrasound scanner are presented in the context of their clinical significance. The beamforming parameters of the scanner were manipulated to produce sound speed errors ranging over +/-8% while imaging a wire target and an attenuating, speckle-generating phantom. For the wire target, these errors produced increases in lateral beam width of up to 320% and reductions in peak echo amplitude of up to 10.5 dB. In the speckle-generating phantom, these errors produced increases in speckle intensity correlation cell area of up to 92% and reductions in mean speckle brightness of up to 5.6 dB. These results are applied in statistical analyses of two detection tasks of clinical relevance. The first is of low contrast lesion detectability, predicting the changes in the correct decision probability as a function of lesion size, contrast, and sound speed error. The second is of point target detectability, predicting the changes in the correct decision probability as function of point target reflectivity and sound speed error. Representative results of these analyses are presented and their implications for clinical imaging are discussed. In general, sound speed errors have a more significant impact on point target detectability over lesion detectability by these analyses, producing up to a 22% reduction in correct decisions for a typical error.

Humans↗
PubMed1968

Neural processing of backwards-speech sounds.

When sounds such as those produced by reverse playback of recorded speech are presented to left and right ears of normal subjects, the sounds arriving at the right ear are more accurately identified than those arriving at the left. These findings are comparable to the right-ear superiority demonstrated with normal speech sounds, and contrast with the left-ear superiority for musical and other non-speech sounds. It is suggested that the neural mechanisms underlying the perception of speech and non-speech sounds are not differentiated along the dimension of conceptual content.

Auditory Perception↗
PubMed1977

Memory for lists of sounds by the bottle-nosed dolphin: convergence of memory processes with humans?

After listening to a list of as many as six discriminably different 2-second sounds, a bottle-nosed dolphin classified a subsequent probe sound as either "old" (from the list) or "new." The probability of recognizing an old probe was close to 1.0 if it matched the most recent sound in the list and decreased sigmoidally for successively earlier list sounds. Memory span was estimated to be at least four sounds. Overall probabilities of correctly classifying old and new probes corresponded closely, as if recognition decisions were made according to an optimum maximum likelihood criterion. The data bore many similarities to data obtained from humans tested on probe recognition tasks.

Animals↗
PubMed1986

Immature sound localisation and abnormal development.

This investigation tested the hypothesis that high risk infants showing immaturity in localisation of a sound stimulus would be more likely to have appreciable neurodevelopmental dysfunction. The cohort comprised 112 infants, 66 of whom were classified as 'high risk'. Every infant underwent a neurological and developmental assessment, a sound localisation response test, and an audiological examination when necessary. The first examination was performed at age 8-9 months and was repeated between six and eight months later. It was found that if the sound localisation response was mature at the first examination normal development could be anticipated at the second examination. If an immature sound localisation response was shown then considerable dysfunction could be anticipated in about half of the infants. It is suggested that special attention be paid to the maturity of the sound localisation response in infants during auditory screening procedures, and an immature response should alert the examiner to the possibility of appreciable abnormality in development.

Auditory Perception↗
PubMed1992

Closing sounds and related complaints after heart valve replacement with St Jude Medical, Duromedics Edwards, Björk-Shiley Monostrut, and Carbomedics prostheses.

OBJECTIVE: To measure the noise produced and related subjective complaints after implantation of four different mechanical heart valve prostheses and to identify further factors related to the patient and prosthesis that influence noise generation and complaints. DESIGN: Sound pressure was measured 5 and 10 cm and 1 m from the point of maximal impulse on the body surface by a calibrated meter in quiet rooms with either a decibel(A) filter or octave filters. The patients were asked about their complaints and examined physically. SETTING: The measurements were conducted in silent rooms of ear, nose, and throat departments. The patients had been operated on either in a university hospital or a community hospital. MAIN OUTCOME MEASURES: Sound pressures of frequency bands and sound pressures measured in dB(A) at various distances. Complaints registerd were: sleep disturbance, disturbance during daytime, "wants a less noisy prosthesis," and "can hear the closing click". PATIENTS: 143 patients after heart valve replacement with St Jude Medical (n = 35), Duromedics Edwards (n = 38), Carbomedics (n = 34) and Björk-Shiley Monostrut (n = 36) prostheses operated on between 1984 and 1988 were matched for valve position, ring size, and body surface area. RESULTS: Duromedics Edwards (33.5 (6) dB(A)) and Björk-Shiley Monostrut valves (31 (4) dB(A)) were significantly louder than St Jude Medical (24 (4) dB(A)) and Carbomedics (25 (6) dB(A)) prostheses (p = 0.0001) (mean (SD)). The louder valves were significantly more often heard by the patients (p = 0.0012) and caused more complaints both during sleep (p = 0.024) and during the daytime (p = 0.07). Patients with these valves were more likely to want a less noisy valve (p = 0.0047). Patients with symptoms were younger, had better hearing, and were more likely to be in sinus rhythm. As well as the type of prostheses, the valve diameter and body height also had an effect on sound emission. CONCLUSIONS: The intensity of the closing click of mechanical valve prostheses was significantly different for various designs. Patient complaints were related to the objectively measured sound pressure. Noise production should be considered when a mechanical valve is selected.

Adult↗
PubMed1997

Sound movement detection deficit due to a brainstem lesion.

Auditory psychophysical testing was carried out on a patient with a central pontine lesion involving the trapezoid body, who presented with a deficit in sound localisation and sound movement detection. A deficit in the analysis of time and intensity differences between the ears was found, which would explain the deficit in detection of sound movement. The impaired detection of sound movement, due to a lesion interfering with convergence of auditory information at the superior olive, suggests this structure to be critical for human sound movement analysis.

Audiometry, Pure-Tone↗
PubMed1992

Effect of methacholine induced bronchoconstriction on the spectral characteristics of breath sounds in asthma.

BACKGROUND: Analysis of breath sounds by digital techniques offers an attractive non-invasive method of monitoring changes in airway calibre. Asthmatic breath sounds have been analysed and related to changes in forced expiratory volume in one second (FEV1). METHODS: Bronchoconstriction was induced with methacholine in six asthmatic subjects on two occasions and changes in FEV1 and breath sound spectra were measured. RESULTS: Audible wheeze appeared after a mean (SE) fall in FEV1 of 35% (6.3%) but the level was not reproducible within patients. The mean and median frequency of the spectra of breath sounds correlated with the percentage of predicted FEV1 (r = -0.5 and -0.6 respectively; p < 0.001). Inclusion of the quartile frequencies in a stepwise multiple regression reduced the residual variance by a further 9%. CONCLUSION: Detecting changes in airway calibre by this method of sound analysis so far produces qualitative data only and will not yield quantitative data in individual patients.

Asthma↗
PubMed1981

Spectral characteristics of normal breath sounds.

An objective and accurate measurement and characterization of breath sounds was carried out by a fast-Fourier-transform frequency-domain analysis. Normal vesicular breath sounds, picked up over the chest wall of 10 healthy subjects showed a characteristic pattern: the power of the signal decreased exponentially as frequency increased. Since the log amplitude vs. log frequency relationships were linear, they could be characterized by the values of the slope and the maximal frequency. The average slope of the power spectrum curves was found to be (in dB/oct +/- SD) 13.0 +/- 1.4 over the base of the right lung, 12.6 +/- 2.4 over the base of the left lung, 9.8 +/- 1.4 over the interscapular region, and 14.4 +/- 4.3 over the right anterior chest. The maximal frequencies of inspiratory and expiratory breath sounds, picked up over the base of the right lung, were (in Hz +/- SD) 446 +/- 143 and 286 +/- 53 (P less than 0.01), over the base of the left lung 475 +/- 115 and 284 +/- 47 (P less than 0.01), over the interscapular region 434 +/- 130 and 338 +/- 77 (P less than 0.05), and over the right anterior chest 604 +/- 302 and 406 +/- 205 (P less than 0.05). Breath sounds picked up over the trachea were characterized by power spectra typical to a broad spectrum sound with a sharp decrease of power at a cut-off frequency that varied between 850 and 1,600 Hz among the 10 healthy subjects studied.

Adult↗
PubMed1982

Vesicular lung sound amplitude mapping by automated flow-gated phonopneumography.

A recently developed automated apparatus capable of determining vesicular lung sound amplitude rapidly and accurately was used to construct detailed inspiratory vesicular sound amplitude maps in eight healthy male subjects to determine the normal amplitude patterns on the chest wall. The sounds were recorded in 2-cm steps along the following lines bilaterally: A, vertically, clavicle to abdomen, 6 cm from the sternal border; B, vertically, from the level of T1 to the lung bases, 6 cm from the spine; and C, horizontally, from the sternal border to the spine at the level of the nipple. Sound amplitude was measured at an airflow rate of 1.3 l/s. The resulting amplitude maps revealed considerable intra- and intersubject variation with frequent amplitude heterophony. Th patterns for the subjects as a group were as follows: series A, amplitude decreasing with distance from the clavicle; series B, amplitude increasing with distance from T1 with a peak at the bases; and series C, approximately equal amplitude at all positions. The findings in series B and C are, in general, consistent with an explanation of ventilation following hydrostatic gradients. The series A pattern and the intersubject variability in amplitude are inconsistent with this explanation and suggest that the inspiratory vesicular sound amplitude is not simply a result of ventilation distribution but involves other as yet undefined factors.

Adult↗
PubMed1993

Detection of tracheal stenosis by frequency analysis of tracheal sounds.

To develop a simple noninvasive method for detecting tracheal stenosis, tracheal sounds were analyzed using fast-Fourier transform. The subjects were all female and included 5 normal volunteers and 13 patients with tracheal stenosis mostly secondary to thyroid cancer (11 extrathoracic and 2 intrathoracic lesions). Tracheal sounds were recorded during spontaneous breathing and were digitized with an analog-to-digital converter. Pulmonary functions, including forced expiratory volume in 1 s (FEV1) expressed as percentage of vital capacity, peak expiratory flow rate (PEFR), the ratio of FEV1 to PEFR (Empey's index), and the ratio of expiratory to inspiratory flow rates at 50% vital capacity, were measured. A computed tomography scan was used to obtain the tracheal minimum cross-sectional area. Whereas PEFR demonstrated a weak correlation with the stenotic area, FEV1%, Empey's index, and the ratio of expiratory to inspiratory flow rates at 50% vital capacity did not. The power of the fast-Fourier transform spectrum of normal tracheal sounds decreased as the frequency increased up to 500 Hz. A small spectral peak was observed at approximately 1 kHz. Patients with significant tracheal stenosis demonstrated an increase in the peak spectral power at approximately 1 kHz and in the mean spectral power from 600 to 1,300 Hz in their tracheal sounds. In patients with extrathoracic lesions, the peak and mean spectral powers correlated well with the area of the stenosis as defined by computed tomography scan. In patients with intrathoracic lesions, abnormalities in the pulmonary functions as well as tracheal sound spectra appeared more evident despite milder stenoses.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed2003

Directional sensitivity of neurons in the primary auditory (AI) cortex: effects of sound-source intensity level.

Transient sounds were delivered from different directions in virtual acoustic space while recording from single neurons in primary auditory cortex (AI) of cats under general anesthesia. The intensity level of the sound source was varied parametrically to determine the operating characteristics of the spatial receptive field. The spatial receptive field was constructed from the onset latency of the response to a sound at each sampled direction. Spatial gradients of response latency composing a receptive field are due partially to a systematic co-dependence on sound-source direction and intensity level. Typically, at any given intensity level, the distribution of response latency within the receptive field was unimodal with a range of approximately 3-4 ms, although for some cells and some levels, the spread could be as much as 20 or as little as 2 ms. Response latency, averaged across directions, differed among neurons for the same intensity level, and also differed among intensity levels for the same neuron. Generally, increases in intensity level resulted in decreases in the mean and variance, which follows an inverse Gaussian distribution. Receptive field models, based on response latency, are developed using multiple parameters (azimuth, elevation, intensity), validated with Monte Carlo simulation, and their spatial filtering described using spherical harmonic analysis. Observations from an ensemble of modeled receptive fields are obtained by linking the inverse Gaussian density to the probabilistic inverse problem of estimating sound-source direction and intensity. Upper bounds on acuity is derived from the ensemble using Fisher information, and the predicted patterns of estimation errors are related to psychophysical performance.

Acoustic Stimulation↗
PubMed1975

Contribution of auditory cortex to sound localization in the monkey (Macaca mulatta).

Monkeys with lesions of auditory cortex were tested for their ability to localize the source of brief sounds. Although those deprived of primary auditory cortex bilaterally were able to indicate the direction of a sound with near-normal acuity, they were unable to locate its source. This dissociation of abilities suggest that the role of auditory cortex in sound localization is not so much sensory or perceptual as it is auditomotor or associative. Thus, sound localization joins loudness, pitch, and most other traditional attributes of sound as dimensions whose discrimination does not depend on auditory cortex. The question would now seem to turn to whether or not auditory cortex is necessary for any sensory discrimination whatever.

Acoustic Stimulation↗
PubMed1996

Sound localization after transection of the commissure of Probst in the albino rat.

1. The ability of rats to localize sounds in space was determined before and after cutting of the commissure of Probst. The commissure of Probst was transected at its midline decussation with a microknife inserted into the brain according to stereotaxic coordinates. Six animals were tested after extensive lesions that destroyed all of the commissure of Probst fibers. An additional animal was tested after a smaller lesion that destroyed most of the commissure of Probst but left some fibers intact. Three control animals were tested before and after surgical intervention that did not involve the commissure of Probst. 2. The animals were tested in a semicircular apparatus with loudspeakers located on the right or left of midline. They were trained to make a response toward the left or right in the direction of the active loudspeaker. Correct reponses were rewarded by delivery of a small quantity of water from spouts located at +30 and -30 degrees azimuth. Tests of sound localization were conducted with a single broadband noise burst, 45 ms in duration, presented at the beginning of each trial. The position of the active loudspeakers was varied from trial to trial and performance at different speaker angles was calculated to determine psychometric curves. Minimum audible angles were estimated by interpolation from a performance level of 75% correct. 3. After postoperative testing was completed, the effectiveness of the lesions was confirmed by cell counts to determine the extent of retrograde degeneration in the dorsal nucleus of the lateral lemniscus (DNLL). These data showed that most of the contralaterally projecting neurons in DNLL underwent retrograde degeneration and the number of neurons was reduced by 60-65%. Ninety to 95% of the contralaterally projecting neurons in the DNLL disappeared within 7 wk after transection of the commissure of Probst. 4. The condition of damaged commissural fibers was further confirmed by tract tracing methods. A unilateral Fluoro-Gold injection was made into the inferior colliculus and the auditory brain stem was examined for retrograde label. No labeled neurons were seen in the contralateral DNLL in cases with complete transection of the commissure of Probst. In addition, the distribution of Fluoro-Gold labeling in other brain stem auditory structures was similar to that seen in normal animals. This result confirmed that the transection of the commissure of Probst was successful and that projections to other auditory structures remained intact. 5. Transection of the commissure of Probst produced marked deficits in midline sound localization. Although sound localization was still possible, there was a degradation in the ability of rats to localize sounds in the horizontal plane. The mean minimum audible angle was elevated 22.1 degrees after destruction of the commissure of Probst compared with a shift of only 2.0 degrees in control animals.

Animals↗
PubMed2001

Responses of auditory cortical neurons to pairs of sounds: correlates of fusion and localization.

When two brief sounds arrive at a listener's ears nearly simultaneously from different directions, localization of the sounds is described by "the precedence effect." At inter-stimulus delays (ISDs) <5 ms, listeners typically report hearing not two sounds but a single fused sound. The reported location of the fused image depends on the ISD. At ISDs of 1-4 ms, listeners point near the leading source (localization dominance). As the ISD is decreased from 0.8 to 0 ms, the fused image shifts toward a location midway between the two sources (summing localization). When an inter-stimulus level difference (ISLD) is imposed, judgements shift toward the more intense source. Spatial hearing, including the precedence effect, is thought to depend on the auditory cortex. Therefore we tested the hypothesis that the activity of cortical neurons signals the perceived location of fused pairs of sounds. We recorded the unit responses of cortical neurons in areas A1 and A2 of anesthetized cats. Single broadband clicks were presented from various frontal locations. Paired clicks were presented with various ISDs and ISLDs from two loudspeakers located 50 degrees to the left and right of midline. Units typically responded to single clicks or paired clicks with a single burst of spikes. Artificial neural networks were trained to recognize the spike patterns elicited by single clicks from various locations. The trained networks were then used to identify the locations signaled by unit responses to paired clicks. At ISDs of 1-4 ms, unit responses typically signaled locations near that of the leading source in agreement with localization dominance. Nonetheless the responses generally exhibited a substantial undershoot; this finding, too, accorded with psychophysical measurements. As the ISD was decreased from ~0.4 to 0 ms, network estimates typically shifted from the leading location toward the midline in agreement with summing localization. Furthermore a superposed ISLD shifted network estimates toward the more intense source, reaching an asymptote at an ISLD of 15-20 dB. To allow quantitative comparison of our physiological findings to psychophysical results, we performed human psychophysical experiments and made acoustical measurements from the ears of cats and humans. After accounting for the difference in head size between cats and humans, the responses of cortical units usually agreed with the responses of human listeners, although a sizable minority of units defied psychophysical expectations.

Action Potentials↗
PubMedDate not supplied

Effects of surrounding tissue on the sound spectrum of arterial bruits in vivo.

Turbulent flow distal to arterial stenoses producers bruits with a characteristic sound spectrum, analysis of which has permitted accurate non-invasive assessment of the residual lumen diameter of the stenosis in the case of the human carotid artery. In contrast, investigators working with in vitro elastic models of arteries or with excised vessels have reported finding mainly resonant spectra of bruits recorded distal to stenoses. We have studied the effects of turbulent flow on the sound spectrum produced at the arterial wall and the influence of surrounding tissue on this spectrum. Aortic, carotid, and femoral stenoses were produced in dogs by external banding of the arteries with 5mm wide Teflon bands. Recordings of bruits made directly on the vessel wall had a sound spectrum made up of 2 components, one due to turbulent flow, and the second to a superimposed resonant spectrum from arterial wall vibration. This was true of 3 kinds of vessels studied. The effects of surrounding tissue on the sound spectrum of arterial bruits was shown by comparing the spectra o bruits recorded directly on the vessel wall, on the freshly closed wound and on the healed wound. The sound properties of the artery in situ are very different from those of exposed or excised vessels or elastic tubes. Although intravascular turbulence may be accurately appreciated at the skin surface, arterial wall resonance in the intact animal is extensively damped by the normal coupling of the artery to its surrounding tissue.

Animals↗
PubMed2003

A monotonic code for sound azimuth in primate inferior colliculus.

We investigated the format of the code for sound location in the inferior colliculi of three awake monkeys (Macaca mulatta). We found that roughly half of our sample of 99 neurons was sensitive to the free-field locations of broadband noise presented in the frontal hemisphere. Such neurons nearly always responded monotonically as a function of sound azimuth, with stronger responses for more contralateral sound locations. Few, if any, neurons had circumscribed receptive fields. Spatial sensitivity was broad: the proportion of the total sample of neurons responding to a sound at a given location ranged from 30% for ipsilateral locations to 80% for contralateral locations. These findings suggest that sound azimuth is represented via a population rate code of very broadly responsive neurons in primate inferior colliculi. This representation differs in format from the place code used for encoding the locations of visual and tactile stimuli and poses problems for the eventual convergence of auditory and visual or somatosensory signals. Accordingly, models for converting this representation into a place code are discussed.

Acoustic Stimulation↗