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PubMed1988

Rate-intensity functions and their modification by broadband noise for neurons in the guinea pig inferior colliculus.

Rate-intensity functions (RIFs) were generated in response to characteristic frequency (CF) tones presented alone and in the presence of broadband noise for neurons in the central nucleus of the inferior colliculus (IC) of the anesthetized guinea pig. Seventy-six percent of the RIFs to CF tones were monotonic (some showing incomplete saturation), and 24% were nonmonotonic. The RIFs to continuous noise were more nonmonotonic than those to CF tones. In continuous or gated noise, the dynamic portion of the RIF to a tone was shifted to a higher tone level, with little change in the dynamic range. Above a threshold noise level, the shift was a linear function of noise level with slope 0.97. Little shift occurred when the noise was inversely gated with respect to the tone burst, suggesting that the underlying mechanism is suppression rather than adaptation. For 63% of units, the maximum discharge rate to a tone in low levels (less than 0-dB spectrum level) of noise (including inversely gated) was greater than to the tone alone. Although many of the effects of noise in the IC reflect peripheral mechanisms, they are supplemented by centrally based processes which enhance the detectability of tone intensity increments in the presence of noise.

Acoustic Stimulation↗
PubMed1988

On the role of the amplitude of the fricative noise in the perception of place of articulation in voiceless fricative consonants.

The current study explores the role of the amplitude of the fricative noise in the perception of place of articulation in voiceless fricative consonants. The amplitude of the fricative noise in naturally produced fricative-vowel utterances was varied relative to the vowel and potential changes in perceptual responses were investigated. The amplitude of the fricative noise for [s] and [s] was reduced such that the amplitude of the noise relative to the vowel was similar to [f] and [O], and, conversely, the amplitude of the fricative noise of [f] and [O] was increased such that the amplitude of the noise relative to the vowel was similar to [s] and [s]. The fricative noise was presented to listeners in both its vowel context and in isolation. Results indicated that, when the spectral properties of the fricative noise and formant transitions are compatible, the perceptual effects of the amplitude manipulation of the amplitude of the noise had a small effect on the overall identification of place of articulation, and when effects emerged, they varied across the different fricative stimuli. Moreover, although decreasing the amplitude of [s] and [s] resulted in an increase in [f] and [O] responses, increasing the amplitude of [f] and [O] did not result in an increase in [s] and [s] responses. Implications of these findings for phonetic feature theories are considered.

Acoustic Stimulation↗
PubMed1989

Comparison of the noise attenuation of three audiometric earphones, with additional data on masking near threshold.

The noise-excluding properties of a standard supra-aural audiometric earphone, a widely used circumaural-supra-aural combination, and an insert earphone sealed to the ear with a vinyl foam eartip were measured in a diffuse-field room complying with ANSI S12.6-1984. Data on attenuation were obtained monaurally with the nontest ear plugged and muffed. Results for the supra-aural earphones generally agreed well with previously reported measurements. A broadband masking noise was used to directly test the ANSI S3.1-1977 permissible background noise levels for measuring to audiometric zero using standard audiometric earphones. This "ANSI noise" raised the average thresholds of 15 normal-hearing test subjects by 3 to 5 dB at the octave frequencies from 500 to 4000 Hz. With a noise conforming to the less stringent OSHA-1983 regulation, average thresholds were elevated 9 to 17 dB. An "ENT office noise" with an overall sound level of 54 dBA raised average thresholds even further, by as much as 29 dB at 500 Hz. Use of the circumaural system in the office noise limited the threshold elevation to 11, 5, 2, and 0 dB at the four octave frequencies tested. With the fully ("deeply") inserted foam eartips, the threshold elevation in the simulated office noise was 2 dB or less at all test frequencies. Actual threshold elevations agreed closely with predictions based on a critical ratio calculation utilizing measured sound field noise levels and measured earphone attenuation values.

Audiometry↗
PubMed1999

Quantifying the distortion products generated by amplitude-modulated noise.

When sinusoidal amplitude modulation (SAM) is applied to noise or tone carriers, the stimuli can generate audible distortion products in the region of the modulation frequency. As a result, when bandpass-filtered SAM noise is used to investigate temporal processing, a band of unmodulated noise is typically positioned at the modulation frequency to mask any distortion products. This study was designed to investigate the distortion products for bandpass noise carriers, and so reduce ambiguity about the form of this distortion and its role in perception. The distortion consists of two distortion-noise bands and a distortion tone at the modulation frequency. In the first two experiments, the level and phase of the distortion tone are measured using two different experimental paradigms. In the third experiment, modulation-frequency difference limens are measured for filtered SAM noise and it is shown that performance deteriorates markedly when the distortion tone is canceled. In a fourth experiment, masked threshold is measured at low frequencies for bands of high-frequency, unmodulated noise with the same levels and spectra as the SAM noises in the earlier experiments. The results confirm that unmodulated noise also produces quadratic distortion which may explain some aspects of earlier reports on remote masking.

Adolescent↗
PubMed2000

Community reaction to aircraft noise: time-of-day penalty and tradeoff between levels of overflights.

A decrease in the level of sound events can compensate for an increase in the level of other events, but noise metrics assume different tradeoffs. Noise metrics also differ in the penalty applied to noise in the evening and to noise in the night, and in the definition of these periods. These two aspects of noise metrics, i.e., the tradeoff and the penalty for the nighttime (23-7h), are investigated. A general model of the relation between SELs of sound events (aircraft overflights) and noise annoyance is presented which allows for a wide range of tradeoffs and time-of-day penalties. The (tradeoff and time-of-day penalty) parameters of the model are fitted to the data from an aircraft noise study conducted around Amsterdam Airport Schiphol, which is especially suited for investigating the tradeoff and time-of-day penalties. It was found that in this study the tradeoff between the levels of events in metrics based on L(Aeq)'s, such as L(Aeq)(24 h), DNL, and DENL, is approximately correct for the prediction of noise annoyance. Furthermore, it was found that the strongest correlation with annoyance is obtained with a nighttime penalty of circa 10 dB. No suitable data were available for further tests of the tradeoff. The result with respect to the nighttime penalty was weakly further supported by the outcome of analyses of the original data from four other aircraft noise surveys (one survey conducted around British airports, and three coordinated surveys carried out around Paris Orly, Amsterdam Schiphol, and Glasgow Abbotsinch).

Aircraft↗
PubMed1988

Response properties of cochlear efferent neurons: monaural vs. binaural stimulation and the effects of noise.

1. Discharge properties of olivocochlear efferent neurons were measured in anesthetized cats. Previous studies of these neurons concentrated on monaural stimulation with tones and found sound-evoked discharge rates rarely exceeded 60 spikes/s (16, 20). In the present study, rates as high as 140 spikes/s were achieved by binaural stimulation and/or the addition of noise. Based on studies on the known effects of electrically stimulating the efferents such high rates of sound-evoked efferent activity probably have significant feedback effects on the auditory periphery. 2. Spontaneous discharge rate (SR) was weakly correlated with threshold among efferent neurons: those with SRs greater than 1 spikes/s were generally more sensitive than spontaneously inactive fibers. The discharge rate measured in the absence of acoustic stimulation was shown to be dependent on stimulation history: some units with zero SR became spontaneously active after several minutes of continuous noise stimulation. 3. For stimulation with monaural tones, efferent excitability varied with characteristic frequency (CF): units with CF less than 10 kHz tended to have lower thresholds, higher discharge rates, and shorter latencies than higher CF units. These differences could be minimized by the addition of broadband noise (see below). 4. When tones were presented to one ear at a time, most efferent units appeared monaural (91%), with roughly two-thirds excited by ipsilateral stimuli and one-third by contralateral stimuli. However, the effects of simultaneous stimulation of the two ears suggested that the great majority of efferent units have binaural inputs: the addition of opposite-ear noise or tones, which presented alone were not excitatory, typically enhanced the response to main-ear stimulation. This type of binaural facilitation was strongest among low-CF efferents when the opposite-ear stimuli were tones, and strongest among high-CF units when the opposite-ear stimulus was broadband noise. 5. The binaural facilitation seen using opposite-ear noise both lowered the threshold (by as much as 40 dB) and increased the discharge rate (by as much as 80%) to tones presented in the main ear. Significant facilitation was seen with noise levels as low as 25 dB SPL or tone levels as low as 30 dB SPL. In general, the weaker the response to monaural stimuli, the stronger the binaural facilitation. 6. The facilitatory effects of stimulation with continuous noise could outlast the stimulus. Persistent increases in efferent sensitivity were documented following 10-min exposures to broadband noise at 85-115 dB SPL.

Acoustic Stimulation↗
PubMed1998

Single olivocochlear neurons in the guinea pig. I. Binaural facilitation of responses to high-level noise.

Single medial olivocochlear (MOC) neurons were recorded from the cochlea of the anesthetized guinea pig. We used tones and noise presented monaurally and binaurally and measured responses for sounds up to 105 dB sound pressure level (SPL). For monaural sound, MOC neuron firing rates were usually higher for noise bursts than tone bursts, a situation not observed for afferent fibers of the auditory nerve that were sampled in the same preparations. MOC neurons also differed from afferent fibers in having less saturation of response. Some MOC neurons had responses that continued to increase even at high sound levels. Differences between MOC and afferent responses suggest that there is convergence in the pathway to olivocochlear neurons, possibly a combination of inputs that are at the characteristic frequency (CF) with others that are off the CF. Opposite-ear noise almost always facilitated the responses of MOC neurons to sounds in the main ear, the ear that best drives the unit. This binaural facilitation depends on several characteristics that pertain to the main ear: it is higher in neurons having a contralateral main ear (contra units), it is higher at main-ear sound levels that are moderate (approximately 65 dB SPL), and it is higher in neurons with low discharge rates to main-ear stimuli. Facilitation also depends on parameters of the opposite-ear sound: facilitation increases with noise level in the opposite ear until saturating, is greater for continuous noise than noise bursts, and is usually greater for noise than for tones. Using optimal opposite-ear facilitators and high-level stimuli, the firing rates of olivocochlear neurons range up to 140 spikes/s, whereas for moderate-level monaural stimuli the rates are <80 spikes/s. At high sound levels, firing rates of olivocochlear neurons increase with CF, an increase that may compensate for the known lower effectiveness of olivocochlear synapses on outer hair cells responding to high frequencies. Overall, our results demonstrate a high MOC response for binaural noise and suggest a prominent role for the MOC system in environments containing binaural noise of high level.

Acoustic Stimulation↗
PubMed2000

Neural responses in the inferior colliculus to binaural masking level differences created by inverting the noise in one ear.

We have measured the responses of inferior colliculus neurons in the anesthetized guinea pig to signals which in human psychophysical experiments reveal a release of masking as a result of binaural processing (the binaural masking level difference: BMLD). More specifically we have used diotic tones at 500 Hz (So) masked by noise that is either identical at the two ears (No) or inverted in one ear (Npi). This combination of signals and noise maskers produces a prominent masking release in humans such that the So signal is about 6-12 dB more detectable in the presence of the Npi noise than the No noise. Low-frequency inferior colliculus neurons are sensitive to the interaural delay of the masking noise and generally respond most to the components nearest their best frequency. Since most inferior colliculus neurons have peaks in their delay functions close to zero interaural time delay this means that while No noise is effective in driving the unit, Npi noise is much less effective. As the level of an So tone was progressively increased in the presence of No and Npi noises, the first response could be either an increase or a decrease in the activity due to the noise. However, because Npi generated little or no activity itself, the predominant response to the So tone was an increase in discharge in this condition. Masked thresholds were defined as the point at which the standard separation D (related to the d' of signal detection theory) = 1 in either direction. BMLDs were measured in single neurons and in the majority of units were in a direction consistent with the psychophysical observations irrespective of the direction of the discharge rate change that occurred at threshold. The lowest masked thresholds always occurred at or near the signal frequency of 500 Hz. An average value of the single unit BMLD around 500 Hz was 3.6 dB (NoSo vs. NpiSo) compared with 6.6 dB for the NoSo versus NoSpi BMLD we had previously reported. This lower magnitude is consistent with the hierarchy of human psychophysical BMLDs.

Acoustic Stimulation↗
PubMedDate not supplied

The effect of various durations of noise exposure on auditory brainstem response, distortion product otoacoustic emissions and transient evoked otoacoustic emissions in rats.

This study was designed to investigate the effect of various durations of noise exposure in animals on physiological responses from the cochlea which are also used clinically in humans: auditory brainstem response (ABR), transient evoked otoacoustic emissions (TEOAEs) and distortion product otoacoustic emissions (DPOAEs). Rats were exposed to 113 dB SPL broad-band noise (12 h on/12 h off) for durations of 3, 6, 9, 12, 15 and 21 days, and tested 24 h after cessation of the noise and again after a period of 6 weeks. ABR threshold to click stimuli and to a 2-kHz tone burst (TB), TEOAE energy content and DPOAE amplitude in the exposed rats were compared to those in a group of control rats not exposed to noise. ABR thresholds (click and TB) were significantly elevated in all exposure duration groups compared to control rats. DPOAE amplitudes and TEOAE energy content were significantly reduced. The mean ABR thresholds following 21 days exposure were significantly greater (click = 100 dB pe SPL; TB = 115 dB pe SPL) than those following 3 days exposure (click = 86 dB pe SPL; TB = 91 dB pe SPL). Linear regression analysis between recorded responses and duration of noise exposure (days) showed a significant increase in ABR thresholds of approximately 0.8-- 1.4 dB/day. TEOAE and DPOAE responses showed no such dependence on noise duration and were already maximally reduced after only 3 days of exposure. This can be explained by the possibility that short noise exposures may cause damage to the early, more active stages of cochlear transduction (as shown by TEOAEs and DPOAEs). As the noise exposure continues, further damage may be induced at additional, later stages of the cochlear transduction cascade (as shown by ABR). Thus, ABR seems more sensitive to noise duration than OAE measures.

Animals↗
PubMed2004

Effects of alcohol and noise on temporary threshold shift in Guinea pigs.

The purpose of this study was to investigate the effects of concomitant exposure to noise and alcohol on the auditory thresholds. Twenty-four guinea pigs were equally divided into three groups: the acute intoxication group, the chronic intoxication group and the control group. Animals in the acute group received single intraperitoneal injections of ethanol (2 g/kg). In the chronic group, alcohol was administered via drinking water (10%, v/v) over a 60-day period. All animals were exposed to a white noise at the intensity of 105 dB A for 30 min. Auditory brainstem response (ABR) thresholds and distortion product otoacoustic emission (DPOAE) levels were measured before, immediately after noise exposure and also 1, 2, and 7 days following exposure. The results showed: first, acute alcohol injection caused a significant, temporary elevation of ABR threshold (4.8 dB in average), while chronic alcohol treatment did not change auditory threshold significantly. Second, noise exposure induced a mean threshold shift of 15.4- 19.7 dB. ABR threshold returned to normal 2 days after exposure. Both acute and chronic alcohol treatment did not alter the magnitude and time course of recovery of the temporary threshold shift (TTS). Third, the mean DPOAE amplitudes decreased at most frequencies following acute injection of alcohol. However, the differences did not reach statistical significance. Fourth, the mean DPOAE levels dropped 3.4-9.6 dB in all groups after noise exposure and returned to normal 1 day to 2 days after noise. There were no significant differences in the amount of DPOAE suppression after noise between the three groups. In summary, we have found that acute and chronic treatment of alcohol in combination with noise did not significantly exacerbate TTS or decrease DPOAE amplitudes relative to noise exposure alone.

Alcoholic Intoxication↗
PubMed1993

Effects of long-term air jet noise and dietary sodium chloride in borderline hypertensive rats.

The hypothesis that simultaneous exposure to a high (8%) sodium chloride diet and behavioral stress (air jet noise) would act synergistically to increase blood pressure was investigated in male borderline hypertensive rats. Rats were fed either a 1% or an 8% sodium chloride diet beginning at 6 weeks of age. Rats in the Air Noise condition were restrained and exposed to random blasts of air jet noise for 2 h/d, 5 d/wk, from 7 to 17 weeks of age. Controls either were placed in identical restrainers and test chambers but not exposed to air jet noise (Restrained Control) or were left undisturbed (Maturation Control). Biweekly indirect blood pressure measurements showed that by 17 weeks of age, the high-sodium chloride diet and air jet noise exposure produced additive increases in blood pressure. Direct blood pressure measurements at 18 weeks of age confirmed the higher systolic pressures in borderline hypertensive rats exposed to both an 8% sodium chloride diet and air jet noise. After ganglionic blockade, the blood pressure of rats in the Air Noise group remained higher than that of Restrained and Maturation Controls, suggesting that the increased blood pressure of air jet noise-exposed rats was not maintained by increased autonomic activity. Blood pressure after maximal vasodilation by hydralazine was increased in rats exposed to both an 8% sodium chloride diet and air jet noise compared with other groups. Baroreceptor reflex sensitivity (tested by graded doses of angiotensin II) did not differ among groups.(ABSTRACT TRUNCATED AT 250 WORDS)

Aircraft↗
PubMed1994

Speech intelligibility and protective effectiveness of selected active noise reduction and conventional communications headsets.

An experiment was conducted to compare both speech intelligibility and noise attenuation of a conventional passive headset (David Clark H10-76) and an electronic Active Noise Reduction (ANR) headset (Bose Aviation) operated with and without its ANR feature. Modified Rhyme Tests were conducted in pink and tank noise, and with and without bilateral phase reversal between earphones. The Bose ANR unit required a significantly higher speech-to-noise (S/N) ratio in both noise environments than the two passive headset systems to maintain equal intelligibility, in part because of its stronger noise reduction and higher required signal level. Articulation Index calculations corroborated the empirical result that the David Clark afforded comparable intelligibility to the Bose ANR device. Bilateral phase reversal proved to be of no benefit, and pink noise proved to be the harsher environment for speech intelligibility. On a speech intelligibility basis alone, the results do not justify the additional cost of the ANR headset; however, when severe noise exposure is at issue, a properly functioning ANR unit may afford more protection than a similar passive headset without electronics, especially in low-frequency noise spectra.

Acoustics↗
PubMed2006

Amplification with digital noise reduction and the perception of annoying and aversive sounds.

Hearing aid users report difficulties using their hearing aids in noisy environments. Problems include understanding speech, loudness discomfort, and annoyance with background noise. Digital noise reduction algorithms have been promoted as a method to solve speech understanding and comfort in noise problems. Research has failed to find improved speech understanding in noise. Little is known about how digital noise reduction affects noise annoyance and aversiveness. The goals of this investigation were to determine how a specific digital noise reduction system affects hearing aid users' perception of noise annoyance and aversiveness and to compare their perceptions to those of normal-hearing listeners. Ratings of noise annoyance and of aversiveness were obtained from 49 participants with moderate sensorineural hearing loss before fitting and after 3 weeks of hearing aid use. Findings were compared to measures obtained from normal-hearing listeners. Perceived annoyance and aversiveness increased with amplification. Annoyance and aversiveness with the hearing aid approximated normal perception. The results of this investigation suggest the need for counseling patients about realistic expectations related to annoyance and aversiveness of sounds at the time of hearing aid fitting.

Adult↗
PubMed1995

Effects of jet engine noise and performance feedback on perceived workload in a monitoring task.

This study examined the effects of exposure to intermittent jet aircraft noise (70 dBA or 95 dBA maximum intensity) and knowledge of results concerning signal detections (hit-KR) on performance efficiency and perceived workload in a 40-min visual vigilance task. The noise featured a Doppler-like quality in which planes seemed to approach from the monitor's left and recede to the right. Perceptual sensitivity (d') was poorer in the context of noise than in quiet but only in the presence of hit-KR. The lack of noise-related performance differences in the absence of hit-KR most likely reflected a "floor effect" rather than some special relation between noise and feedback. When compared to subjects performing in quiet, those who operated in noise were less able to profit from hit-KR, a result that may reflect the effects of noise on information processing. In addition to its negative effects on signal detectability, noise elevated the perceived workload, as measured by the NASA-TLX. This effect was robust; it was independent of the presence of hit-KR, even though hit-KR generally lowered the overall level of perceived workload. The results provide the initial experimental demonstration that perceived workload is a sensitive measure of the effects of aircraft noise in monitoring tasks.

Adolescent↗
PubMed2004

Acoustic communication in noise: regulation of call characteristics in a New World monkey.

This study on common marmosets Callithrix jacchus is the first to examine noise-dependent mechanisms of vocal plasticity in a New World monkey. Since acoustic communication can be considerably impaired by environmental noise, some animals have evolved adaptations to counteract its masking effects. The studied marmosets increased the sound level of their spontaneous calls in response to increased levels of white noise broadcast to them. Possibly, such noise-dependent adjustment of vocal amplitude serves to maintain a specific signal-to-noise ratio that is favourable for signal production. Concurrently, the adjustment of vocal amplitude can maintain a given active space for communication. In contrast to some bird species, no noise-induced increase in the number of syllables per call series could be found, showing that an increased serial redundancy of vocal signals was not used to communicate under noisy conditions. Finally, we examined a possible noise-dependent prolongation of vocal signals. This approach was guided by the findings of perceptional studies, which suggest an increased detection probability of prolonged signals in noise by temporal summation. Marmosets indeed increased the duration of their call syllables along with increasing background noise levels. This is the first evidence of such mechanism of vocal plasticity in an animal communication system.

Adaptation, Physiological↗
PubMed1995

Effects of traffic noise on sleep: a review.

Examination of the effect of noise on sleep indicated the following: 1) Views differ on habituation to noise. 2) REM sleep in all-night sleep decreases with exposure to noise. The probability of transient changes of REM sleep to other stages is low. REM sleep induction may be disturbed by noise exposure, but once it has been induced, changes to other stages or waking occur only to a small extent. 3) A transient decrease in sleep spindles is caused by noise exposure, but the number of sleep spindles for all-night sleep increases. Sleep disturbance by noise is compensated for by an increase in sleep spindles during periods of silence, possibly indicating sleep maintenance. 4) Under certain circumstances, subjective sleep is a better indicator of the effects of noise on sleep than objective sleep parameters determined by sleep polygraphy. 5) There is a linear dose-response relationship between the peak noise level and the rate of stage shift or waking. The threshold of the noise effect is about 40 dBA.

Humans↗
PubMed1975

Effects of noise bands on contralateral pure tone adaptation.

The purpose of this study was to investigate the changes in threshold tone decay which result from contralaterally presented stimuli at an intensity less than interaural crossover. Five tone decay tests were administered at both 1,000 Hz and 2,000 Hz to 25 normal hearing adults. At each test frequency five contralateral conditions (no competing noise, white noise, narrow band noise centered at the test frequency, narrow band noise centered below the test frequency, and narrow band noise centered above the test frequency), were presented at 40 db above detection threshold to the nontest ear. Results showed a significant shift in tone decay scores when the conditions of white noise and narrow band noise centered around the test frequency were compared to the condition of no competing noise. A shift was seen at both frequencies but that occuring at 2,000 Hz was significantly greater than the shift at 1,000 Hz. No significant increase in tone decay was found for contralateral noise bands above or below the test frequencies.

Adolescent↗
PubMed2000

Noise exposure and public health.

Exposure to noise constitutes a health risk. There is sufficient scientific evidence that noise exposure can induce hearing impairment, hypertension and ischemic heart disease, annoyance, sleep disturbance, and decreased school performance. For other effects such as changes in the immune system and birth defects, the evidence is limited. Most public health impacts of noise were already identified in the 1960s and noise abatement is less of a scientific but primarily a policy problem. A subject for further research is the elucidation of the mechanisms underlying noise-induced cardiovascular disorders and the relationship of noise with annoyance and nonacoustical factors modifying health outcomes. A high priority study subject is the effects of noise on children, including cognitive effects and their reversibility. Noise exposure is on the increase, especially in the general living environment, both in industrialized nations and in developing world regions. This implies that in the twenty-first century noise exposure will still be a major public health problem.

Hearing Disorders↗