Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “NOISE”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 613 records · Page 34Linked to original sources

[Noise--a stress factor in occupational and other environments].

The effects of noise on health can be divided into aural effects and extraaural effects. The following review describes - after some historical remarks - first the physical and technical basis of noise analysis. The definition of "equivalent continuous sound level" (Lm) and "rating sound level" (Lr) is given. Extraaural noise effects mainly come from the environment (traffic noise, construction noise on building sites). One must distinguish physical and vegetative reactions. An important extraaural effect is the disturbance of sleep. The objectivation and quantification of extraaural effects of noise on health is very difficult because there exist a lot of disturbing factors. The most important aural effect of noise on health is the occupational hearing loss. To assess these effects, information about physiology, pathophysiology and clinical indications of noise induced labyrinthine deafness is necessary. As examples results of investigations into the effect of noise on arc welders, professional musicians and building workers are presented. Generation of noise should be minimised by technical methods, exposure to noise by personal protection. The methods for occupational medical check-up of the employment accident insurance fund are specially mentioned. The results of these preventive procedures can be seen in the decreasing numbers of occupational hearing loss.

Audiometry, Pure-Tone↗

Direct assessment of recombination noise in semiconductors using electron beam-induced conductivity.

The level of internal noise of the transistors, diodes, and other semiconductor components limits the successful design of any low noise electronic system. All types of noise, namely, Johnson, 1/f, and so forth, are generated due to activity of crystalline defects such as vacancies, dislocations, and others. The intensity of the electron scattering and recombination processes, inflicted by defects (traps), controls the level of noise. Dependent on the dynamic operation condition of semiconductor devices, such as external biases and level of current injection, the traps will generate certain type and level of noise. Material growth or device processing technologies could introduce all kind of defects. Therefore, characterization of the semiconductor wafer in the early stages of processing (at least before packaging) could help to predict the level of noise due to the type and density of defects present on the wafer. Sorting out bad semiconductor chips could save money and effort in the radio frequency design of low-noise circuits. This current study focuses on 1/f noise modeling, which involves most powerful generators of noise and linear defects, named dislocations. The study also examines the possibility of assessing this noise by quantitative electron beam-induced conductivity (EBIC) measurements. These defects could be found in the bulk as well as at the epitaxial interfaces of a semiconductor device. The nanoscale size of these defects makes the scanning electron beam an instrument of choice for the proposed study. Conventional EBIC produces images of the defects, where contrast is proportional to the recombination rate at the site of a defect. Since contrast is measured as a fraction of one percent, the relative nature of contract value precludes quantitative measurements of the recombination rate, thus making quantitative assessment of 1/f noise impossible. In our model, using the Boltzman continuity equation, the recombination-generation processes per unit of length of a dislocation was defined for two operational conditions of EBIC, namely, for low and high intensity of an electron beam. The experimental technique of the quantitative measurement of carrier recombination (Mil'shtein 2001) consists of taking two EBIC scans along the selected defect at two different beam intensities, digitally subtracting the first scan from the second one and normalizing the result to the size of the electron range. The value of the recombination rate, extracted from the model, could then be used to predict the level of 1/f noise in the tested semiconductor sample.

Journal Article↗

Spatial and temporal characteristics of physiological noise in fMRI at 3T.

RATIONALE AND OBJECTIVES: Physiological noise in blood oxygen level-dependent functional magnetic resonance imaging (BOLD fMRI) has been shown to have characteristics similar to the BOLD signal itself, suggesting that it may have a vascular dependence. In this study, we evaluated the influence of physiological noise in fMRI as revealed by the differences in vasculature sensitivity of gradient-echo echo-planar imaging (GE-EPI) and spin-echo EPI (SE-EPI). MATERIALS AND METHODS: The contribution of physiological noise to the fMRI signal during activation of the visual cortex was assessed by comparing its temporal characteristics with respect to echo time (TE), using both GE-EPI and SE-EPI. The correlation of the noise in fMRI with apparent diffusion coefficient (ADC) and the number of components required to describe its variance, as determined by principal-component analysis (PCA), were also assessed. RESULTS: The SE-EPI data were less affected by a TE-dependence of noise, in contrast to the apparent physiological noise in GE-EPI. Voxel-wise analysis revealed that total apparent noise increased as ADC values increased, and the relationship was different for GE-EPI and SE-EPI. PCA revealed that while the number of components characterizing the noise in SE-EPI data increased in a TE-dependent manner, approaching that of white noise at long echo time, the number of components from GE-EPI data was TE-independent. CONCLUSIONS: The difference in sensitivities to physiological noise between SE-EPI and GE-EPI suggests that extravascular BOLD processes around draining veins contribute significantly to physiological noise in BOLD fMRI, and the suppression of this noise component may enhance SE-EPI BOLD sensitivity at higher fields.

Echo-Planar Imaging↗

Effects of noise on the performance of rats in an operant discrimination task.

Two experiments examined the effect of the presentation of an irregular, moderate intensity auditory stimulus ('noise') on the performance of rats in an operant discrimination task. In Experiment 1, rats first learned to press a lever in the presence of a visual stimulus but not in its absence. Discrimination performance was impaired during subsequent exposure to noise. In Experiment 2, different groups of rats learned the discrimination task under a noise or a no-noise condition. Thereafter, all rats were tested under each noise condition. Discrimination performance was best when the noise condition at test was identical to the noise condition at training. These results were discussed in the framework of arousal, distraction, generalization decrement, and contextual occasion setting. They point to the necessity of using a 2x2 factorial design in human and animal research on noise effects, with noise condition at training (noise present or absent) and noise condition at test (noise present or absent) as factors.

Journal Article↗

Using electrical noise to enhance the ability of humans to detect subthreshold mechanical cutaneous stimuli.

Stochastic resonance (SR) is a phenomenon wherein the response of a nonlinear system to a weak input signal is optimized by the presence of a particular, nonzero level of noise. Our objective was to demonstrate cross-modality SR in human sensory perception. Specifically, we were interested in testing the hypothesis that the ability of an individual to detect a subthreshold mechanical cutaneous stimulus can be significantly enhanced by introducing a particular level of electrical noise. Psychophysical experiments were performed on 11 healthy subjects. The protocol consisted of the presentation of: (a) a subthreshold mechanical stimulus plus electrical noise, or (b) no mechanical stimulus plus electrical noise. The intensity of the electrical noise was varied between trials. Each subject's ability to identify correctly the presence of the mechanical stimulus was determined as a function of the noise intensity. In 9 of the 11 subjects, the introduction of a particular level of electrical noise significantly enhanced the subject's ability to detect the subthreshold mechanical cutaneous stimulus. In 2 of the 11 subjects, the introduction of electrical noise did not significantly change the subject's ability to detect the mechanical stimulus. These findings indicate that input electrical noise can serve as a negative masker for subthreshold mechanical tactile stimuli, i.e., electrical noise can increase the detectability of weak mechanical signals. Thus, for SR-type effects to be observed in human sensory perception, the noise and stimulus need not be of the same modality. From a bioengineering and clinical standpoint, this work suggests that an electrical noise-based technique could be used to improve tactile sensation in humans when the mechanical stimulus is around or below threshold. (c) 1998 American Institute of Physics.

Journal Article↗

Binocular and monocular detection of Gabor patches in binocular two-dimensional noise.

Contrast thresholds for detecting sine-wave Gabor patches in two-dimensional externally added random-pixel noise were measured. Thresholds were obtained for monocular and binocular signals in the presence of spatial correlated (identical) and uncorrelated (independent) noise in the two eyes. Measurements were obtained at four different spectral densities of noise (including zero). Thresholds were higher for monocular stimuli than for binocular, and higher in the presence of correlated noise compared to uncorrelated noise. The magnitude of binocular summation, similar in correlated and uncorrelated noise, decreased with increasing noise strength. The independent contributions of internal noise and sampling efficiency to detection were analysed. Sampling efficiencies were higher for binocular than for monocular viewing for both types of noise, with values being higher with uncorrelated noise. Binocular stimuli showed a lower equivalent noise level compared to the mean monocular case for both types of noise.

Contrast Sensitivity↗

Noise and single channels activated by excitatory amino acids in rat cerebellar granule neurones.

1. Glutamate-receptor ion channels in rat cerebellar granule cells maintained in explant cultures have been investigated with patch-clamp methods. Properties of these channels were determined from noise analysis of whole-cell currents and from noise and single-channel currents recorded in outside-out membrane patches. 2. Glutamate (10-20 microM) evoked two types of response. Some granule cells gave small inward currents accompanied by clear increases in current noise ('large noise' responses), whereas other cells gave larger inward currents and small noise increases ('small noise' responses). 3. A mean single-channel conductance (gamma) of 46.6 pS was estimated for glutamate from four 'large noise' cells. A mean gamma value of 8.4 pS was estimated for seven other 'large noise' cells. The results suggest that in these latter cells glutamate activated both large (approximately equal to 50 pS) and small conductance (approximately equal to 140 fS) channels. 4. Applications of aspartate (10-30 microM) or N-methyl-D-aspartate (NMDA, 10-30 microM) produced small inward currents and large increases in noise; gamma noise = 48.5 pS (aspartate) and 46.7 pS (NMDA). 5. Large single-channel currents were evoked by glutamate, aspartate and NMDA in outside-out patches. The mean conductance values obtained for the largest amplitude openings were: gamma(glutamate) = 49.5 pS, gamma(aspartate) = 51.5 pS, and gamma(NMDA) = 53.0 pS. For each agonist, these 50 pS openings comprised 75-85% of the completely resolved currents in each patch. Openings to 40 and 30 pS conductance levels accounted for 10-15% and 3-7% of the total, and the presence of apparently direct transitions between these levels and the 50 pS level suggests they are sublevels of the same multi-conductance channels. 6. A mean channel conductance of 22.9 pS was estimated from noise evoked by quisqualate (10-30 microM). Single-channel currents were examined in four patches. In two, quisqualate evoked predominantly small currents of two amplitudes, gamma = 8.4 pS and 16.5 pS; some 50 pS openings were also present. In the other two patches, most openings were 50 pS events. 7. Granule cells gave inward currents to kainate (10-30 microM), and a mean conductance of 3.1 pS was estimated from kainate noise. In patches in which aspartate or NMDA produced mainly 50 pS openings, more than 74% of the single-channel currents evoked by kainate were of smaller amplitude, with mean conductances of gamma = 8.1 and 15.1 pS.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗

A quantitative investigation of additive noise reduction for active matrix flat-panel imagers using compensation lines.

A quantitative investigation of a technique for reducing correlated noise in indirect detection active matrix flat-panel imagers has been reported. Correlated noise in such systems arises from the coupling of electronic noise, originating from fluctuations in external sources such as power supplies and ambient electromagnetic sources, to the imaging array via its address lines. The noise reduction technique involves the use of signals from columns of compensation line pixels located in relatively close proximity to the columns of normal imaging pixels on the array. Compensation line pixels are designed to be as sensitive to externally-coupled noise as columns of normal imaging pixels but are insensitive to incident radiation. For each imaging pixel, correlated noise is removed by subtracting from the imaging pixel signal a signal derived from compensation line pixels located on the same row. The effectiveness of various implementations of this correction has been examined through measurements of signal and noise from individual pixels as well as of noise power spectra. These measurements were performed both in the absence of radiation as well as with x rays. The effectiveness of the correction was also demonstrated qualitatively by means of an image of a hand phantom. It was found that the use of a single compensation line dramatically reduces external noise through removal of the correlated noise component. While this form of the correction increases non-radiation-related uncorrelated noise, the effect can be largely reduced through the introduction of multiple compensation lines. Finally, a position-dependent correction based on compensation lines on both sides of the array was found to be effective when the magnitude of the correlated noise varied linearly across the array.

Electronics↗

Differences in auditory performance between monaural and dichotic conditions. I: masking thresholds in frozen noise.

Thresholds of a 5-ms, 1-kHz signal were determined in the presence of a frozen-noise masker. The noise had a flat power spectrum between 20 Hz and 5 kHz and was presented with a duration of 300 ms. The following interaural conditions were tested with four listeners: Noise and signal monaural at the same ear (monaural condition, NmSm), noise and signal identical at both ears (diotic condition, NoSo), noise identical at both ears and signal monaural (dichotic condition, NoSm) and uncorrelated noise at the two ears and signal monaural (NuSm). The signal was presented at a fixed temporal position with respect to the frozen noise in all measurements and thresholds were determined for different starting phases of the carrier frequency of the signal. Variation of the carrier phase strongly influenced the detection in the diotic condition and the masked thresholds varied by more than 10 dB. The pattern of thresholds for the monaural condition was less variable and the thresholds were generally higher than for the diotic condition. The monaural-diotic difference for specific starting phases amounted to as much as 8 dB. Comparison measurements using running noise maskers revealed no such difference. This relation between monaural and diotic thresholds was further investigated with eight additional subjects. Again, monaural and diotic thresholds in running noise were identical, while in frozen noise, diotic thresholds were consistently lower than monaural thresholds, even when the ear with the lower NmSm threshold was compared. For the starting phase showing the largest monaural-diotic difference, the thresholds for NoSm lay between the monaural and the diotic values. At other starting phases, the NoSm threshold was clearly lower than both the NmSm and the NoSo threshold. One possible explanation of the observed monaural-diotic differences relates to contralateral efferent interaction between the right and the left hearing pathway. A prediction based on this explanation was verified in a final experiment, where frozen-noise performance for NmSm was improved by simultaneously presenting an uncorrelated running noise to the opposite ear.

Acoustic Stimulation↗

Interaction of baseline synaptic noise and Ia EPSPs: evidence for appreciable negative correlation under physiological conditions.

1. In the anesthetized cat, simultaneous intracellular recordings from pairs of spinal motoneurons were undertaken to see whether the amplitude of single-fiber excitatory postsynaptic potentials (EPSPs) in both cells fluctuated in a coordinated manner that would indicate correlative mechanisms at either pre- or post-synaptic level. Although these recordings revealed correlated fluctuations in the baseline, the single-fiber Ia/EPSPs recorded with the spike-triggered averaging technique exhibited no correlated fluctuations and, unexpectedly, virtually no increase in baseline variance associated with the EPSP. However, the fact that these experiments were carried out under conditions of high baseline synaptic noise (i.e., with muscle stretch) may have influenced the outcome because of interaction between EPSP and synaptic noise, and this possibility was evaluated explicitly. 2. A given connection was studied under low noise by electrically stimulating a single Ia fiber in the absence of muscle stretch. The same connection was analyzed under conditions of high noise by activating the fiber and all other stretch receptor afferents with muscle stretch and by using spike-triggered averaging to extract the EPSP. The differences in mean EPSP amplitude at a given connection under conditions of low noise and high noise were minimal. 3. Fluctuations in EPSP amplitude were then determined to see whether these were influenced by presence of baseline synaptic noise and whether the interaction was nonlinear. Two methods were used to measure EPSP fluctuations: measurement of the variance associated with the EPSP, and determination by the use of deconvolution methods of the discrete amplitude components associated with the EPSP. 4. An increase in baseline variance was observed during the EPSP evoked under low noise conditions at all six connections studied in this way. This increase disappeared at two of these connections when examined under high noise. This may help to explain the results obtained in pairs of motoneurons. 5. The deconvolution results were used to calculate the variance of the noise-free EPSP. This was found to differ from the variance of the EPSP amplitude distribution measured directly from the change in baseline variance associated with the EPSP. Analytic techniques suggested that this difference could be explained in most cases by negative correlation between the EPSP and baseline synaptic noise. These considerations led to an analytic method to assess the reliability of the deconvolution result. 6. Simulation studies revealed that the baseline variance increase associated with the EPSP is also highly dependent on the correlation between signal and noise.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Detection in fixed and random noise in foveal and parafoveal vision explained by template learning.

Foveal and parafoveal contrast detection thresholds for Gabor and checkerboard targets were measured in white noise by means of a two-interval forced-choice paradigm. Two white-noise conditions were used: fixed and twin. In the fixed noise condition a single noise sample was presented in both intervals of all the trials. In the twin noise condition the same noise sample was used in the two intervals of a trial, but a new sample was generated for each trial. Fixed noise conditions usually resulted in lower thresholds than twin noise. Template learning models are presented that attribute this advantage of fixed over twin noise either to fixed memory templates' reducing uncertainty by incorporation of the noise or to the introduction, by the learning process itself, of more variability in the twin noise condition. Quantitative predictions of the template learning process show that it contributes to the accelerating nonlinear increase in performance with signal amplitude at low signal-to-noise ratios.

Artifacts↗

Characterizing human perceptual inefficiencies with equivalent internal noise.

A widely used method for characterizing and comparing inefficiencies in perceptual processes is the method of equivalent internal noise--the amount of random internal noise necessary to produce the degree of inefficiency exhibited by the perceptual system in processing [J. Opt. Soc. Am. 46, 634 (1956)]. One normally estimates the amount of equivalent internal noise by systematically increasing the amount of external noise added to the signal stimulus and observing how threshold--signal stimulus energy required for an observer to maintain a given performance level--depends on the amount of external noise. In a variety of perceptual tasks, a simple noisy linear amplifier model [D. Pelli, Ph.D. dissertation (University of Cambridge, Cambridge, UK 1981)] has been utilized to estimate the equivalent internal noise Ninternal by fitting of the relation between threshold contrast c tau and external noise N(ext) at a single (d') performance level: c tau 2 =(d'/beta)2(N(ext)2 + Ninternal2). This model makes a strong prediction: Independent of observer and external noise contrast, the ratio between two thresholds at each external noise level is equal to the ratio of the two corresponding d' values. To our knowledge, this potential test for the internal consistency of the model had never been examined previously. In this study we estimated threshold ratios between multiple performance levels at various external noise contrasts in two different experiments: Gabor orientation identification, and Gabor detection. We found that, in both identification and detection, the observed threshold ratios between different performance levels departed substantially from the d' ratio predicted by the simple noisy linear amplifier model. An elaborated perceptual template model [Vision Res. 38, 1183 (1998)] with nonlinear transducer functions and multiplicative noise in addition to the additive noise in the simple linear amplifier model leads to a substantially better description of the data and suggests a reinterpretation of earlier results that relied on the simple noisy linear amplifier model. The relationship of our model and method to other recent parallel and independent developments [J. Opt. Soc. Am. A 14, 2406 (1997)] is discussed.

Artifacts↗

Ag-AgCl electrode noise in high-resolution ECG measurements.

The authors measured the noise and impedance from face-to-face Ag-AgCl electrode pairs, as well as the noise from Ag-AgCl electrodes placed on the human body surface, in the frequency band from 0.5 Hz to 500 Hz, which corresponds to high-resolution ECG measurements. Electrode noise and electrode impedance were measured simultaneously to compare electrode noise with the thermal noise from the real part of electrode impedance. The results show that electrode noise depends on electrode area, electrolytic gel, the patient, and the placement site. In the frequency band from 0.5 Hz to 500 Hz, root-mean-square electrode noise is typically less than 1 microV for electrodes placed face-to-face and ranges from 1 microV to 15 microV for electrodes on the body surface. The noise spectral density increases at low frequencies as 1/fa and it is always higher than the thermal noise from the real part of the electrode impedance. There is a high correlation between electrode dc offset voltage and electrode noise. Thus, offset voltage measurements allow identification of noise from low-noise electrodes.

Algorithms↗

Factors influencing subjective noise sensitivity in an urban population.

This study was designed to define the individual variables influencing subjective noise sensitivity in an urban population and to investigate the distribution of subjective noise sensitivity with regard to noise exposure. A general questionnaire, a ten-graded noise annoyance scale, the Weinstein's Noise Sensitivity Scale, and the Eysenck Personality Questionnaire were applied to a sample of 413 inhabitants of Belgrade. Distribution of noise sensitivity scores was normal and independent of noise exposure. No significant differences in average noise sensitivity scores were observed concerning gender and exposure to low (Leq < 55 dBA), and high level of traffic noise (Leq > 65 dBA). Multiple regression analysis revealed that neuroticism was the best individual predictor for SNS, for both sexes in the noisy area and for women only, in the quiet area (P < 0.001). Age, education level and introversion were not significantly related to noise sensitivity. Positive relation between reported noise annoyance and noise sensitivity was highly significant (P < 0.0001).

Journal Article↗

Masking-level difference for spondaic words in 2000-msec bursts of broadband noise.

One protocol developed for the Tonal and Speech Materials for Auditory Perceptual Assessment audio compact disc was the masking-level difference (MLD) for spondaic words in which the words and broadband noise were mixed and recorded at 16 selected signal-to-noise ratios. Four words were recorded at each level. Because it was impossible to monitor the word presentations at negative signal-to-noise ratios, a different paradigm was devised in which the spondaic words were embedded in 2000-msec bursts of noise. Before the materials were finalized for the compact disc, two experiments studied the perceptual characteristics of the paradigm. Experiment I was performed to determine the characteristics of the MLD for spondaic words in 2000-msec bursts of noise at 70 dB SPL. An unexpected finding was that the mean SoNo thresholds were at signal-to-noise ratios 3-4 dB lower than previously reported spondaic word thresholds in continuous broadband noise. Experiment II examined this discrepancy with the spondaic words embedded in continuous noise and in the 2000-msec noise bursts. The results confirmed the 3-4 dB difference between thresholds for the two masker conditions. Based on the pilot data, the spondaic words embedded in 2000-msec bursts of broadband noise at signal-to-noise ratios of 0 dB to -30 dB were recorded on the compact disc in the S pi No paradigm. In the compact disc trials, which involved 120 subjects with normal hearing, the MLDs for the spondaic words recorded on the compact disc were measured on 60 subjects at each of two noise levels.(ABSTRACT TRUNCATED AT 250 WORDS)

Acoustic Stimulation↗

Contrast detection in noise: a new method for assessing the visual function in cataract.

The detectability of a signal decreases in the presence of externally added visual noise. A linear relation exists between the energy of a signal at threshold and the spectral density of the added visual noise. This relation, represented by contrast detection in noise function, allows a given loss in contrast sensitivity (CS) to be attributed to an increase in the internal intrinsic noise and/or a decrease in the detection efficiency of the observer. Intrinsic noise gives a measure of the random background noise within the visual system, whereas detection efficiency is a measure of how effectively the observer utilizes the available stimulus information. Recent work shows that neural dysfunction produces a decrease in the detection efficiency, whereas optical deficits produce a change in the intrinsic noise only. We investigated whether the CS loss in cataract can be attributed to either a change in intrinsic noise, in detection efficiency, or both. Contrast detection in noise functions was measured for 10 uniocular cataract patients. Comparison between the two eyes showed no significant difference in detection efficiency, although the intrinsic noise increased significantly in the cataractous eye. The data suggest that detection efficiency may provide a measure of neural visual function behind a cataract and, conversely, that intrinsic noise provides a measure of the visual effect of the cataract itself. We discuss the implications of intrinsic noise as a measure of cataract for both clinical assessment and research.

Aged↗

Hearing threshold and heart rate in men after repeated exposure to dynamic muscle work, sinusoidal vs stochastic whole body vibration and stable broadband noise.

Changes in the temporary hearing threshold ( TTS2 ) and heart rate (HR) were examined in subjects exposed to stable noise, whole body vibration and dynamic muscular work at a dry-bulb temperature of 30 degrees C. The exposure combinations consisted of three categories of dynamic muscular work with varying loads ( 2W , 4W , 8W ), of two categories of noise and of three categories of vibration. The noise categories were: (1) no noise, and (2) stable, broadband (bandwidth 0.2-16.0 kHz) A-weighted noise with an intensity of 90 dB. The vibration categories were: (1) no vibration, (2) sinusoidal whole body vibration (Z-axis) with a frequency of 5 Hz, and (3) stochastic broadband (bandwidth 2.8-11.2 Hz) whole body vibration. A single test consisted of a control period of 30 min, three consecutive exposure periods of 16 min, each followed by a 4-min post-exposure interval and a recovery period of 15 min. The results of the variance analyses indicated that noise had the most notable effect on the TTS2 values at the hearing frequencies of both 4 and 6 kHz. Of the paired combinations, noise plus vibration and noise plus dynamic muscular work caused the most obvious combined effects. The combined effect of all three factors (noise, vibration and work) on the TTS2 values after three consecutive exposure periods was significant at the 2.5% level at the 4 kHz hearing frequency and at the 5% level at the 6 kHz hearing frequency. The added effect of vibration on enhanced TTS2 values was particularly clear when the vibration was stochastic and when the subjects had a low ( 2W ) working efficiency. Increasing the working efficiency, on the other hand, seemed to retard increases in the hearing threshold. Thus TTS2 values seemed to reflect the changes in HR values. It is as if the low rate of cardiovascular activity during light dynamic muscular work had enabled the manifestation of the cardiovascular effects of noise and vibration; during strenuous dynamic muscular work, however, the high rate of cardiovascular activity aimed in some way at compensating for the effects of noise and vibration on blood circulation.

Adult↗

Novel long-term cardiovascular effects of industrial noise.

Baboon subjects were instrumented with indwelling arterial catheters for continuous measurement of blood pressure and heart rate before, during, and after exposure to industrial noise eight hours daily. Initial exposure to noise produced transient, acute elevations of systolic and diastolic blood pressures and heart rates at noise onset, which habituated over the course of noise exposure. Chronic exposure to noise lowered blood pressure and heart rate not only during noise, but particularly after daily noise offset. Blood pressures returned toward baseline after noise exposure was terminated. Plasma catecholamines were also decreased during noise exposure. A control animal which received only masking noise did not demonstrate decreases in cardiovascular parameters. The possibility of classically conditioned associations of noise onset with feeding was discussed.

Animals↗