Amplitude discrimination of sinusoids and narrow-band noise with Rayleigh properties.

The ability of human observers to discriminate differences in the amplitude of sinusoids and narrow-band noises was measured by the rating method of detection theory. Although each sinusoid (always 1000 Hz) was presented at a fixed amplitude, its amplitude on any trial was drawn from one of two Rayleigh probability distributions that differed in mean amplitude: a signal distribution and a noise distribution. Similarly, the amplitudes of the narrow-band noises were distributed as the Rayleigh distribution by virtue of the reciprocal relation between their bandwidth (100 Hz centered on 1000 Hz) and duration (10 msec). The obtained psychometric functions showing the area under the ROC as a function of signal-to-noise ratio were similar for both kinds of signals and were displaced, on average, about 4 dB from an ideal observer's function. The slopes of the obtained functions were similar to those of an ideal observer using 1 degree of freedom--half the number available in Rayleigh noise.     

Frequency discrimination near masked threshold

Frequency DLs (Δf) at 1000 Hz were obtained in quiet and under masking conditions similar to those used in pitch-shift experiments, narrow-band noise at levels of 60, 80, and 100 dB SPL and tones at 15 dB SL or less. The Δfs were obtained by means of a tracking task in which the S controlled the input voltage to a frequency modulator. Characteristic improvement was seen when Δf was plotted as a function of sensation level. However, noise level itself was a significant factor, with more intense noise resulting in larger Δfs for tones of equal sensation level re masked threshold. This departure from previous findings is attributed to the signal and noise levels used, although the possibility exists that it is due to the use of modulated tones.     

Binaural summation of loudness: Noise and two-tone complexes

A series of six experiments used the method of magnitude estimation to assess how the two ears sum the loudness of stimuli with various spectra. The results showed that the binaural system sums loudnesses by at least two distinct sets of rules, one applicable to narrow-band stimuli (complete loudness summation), another to wide-band noises (partial summation, dependent on level). The main findings were: (1) Narrow-band noise (Vi-octave bands at 1,000 Hz) showed complete binaural loudness summation, like that previously reported for pure tones (Marks, 1978a). At all but low SPL, a monaural stimulus must be 10 dB greater than a binaural stimulus to be equally loud; a stimulus ratio of 10 dB corresponds to a loudness ratio of 2:1 on Stevens’ sone scale. (2) Wide-band noise (300-4,800 Hz) showed only partial summation, the subadditivity being confined largely to levels below about 60 dB SPL. This result obtained both with bands of white noise (flat spectrum) and pink noise (—3 dB/ octave). (3) Binaural summation of two-tone complexes depended slightly on frequency spacing. Narrow spacing (860 and 1,160 Hz) gave summation equal to about 10 dB, like that of narrowband noises and single tones, whereas wider spacing (675 and 1,475 Hz) gave less summation, equal to about 9 dB, and more like wide-band noise; however, a very wide spacing (300 and 4,800 Hz) gave summation like that of narrow-band noises and single pure tones.     

Psychometric functions for the discrimination of differences in intensity of gaussian noise

A new theory of sensory functioning by Laming predicts how the shape of the psychometric function depends on the context in which a signal is presented. The discrimination of intensities of noise was therefore studied with four different stimulus configurations. In one, observers discriminated between two separate noise samples that differed in intensity. In accordance with the theory, a normal probability integral provided a better fit to each observer's data than either of two other functions: a normal integral with respect to the square of the difference, or a normal integral with respect to the fourth power of the difference. In a second task, observers detected an increment in a continuous noise. For eight out of nine sets of data, a square-law function provided a better fit than either a normal integral or fourth-power function. A third task asked observers to decide which of two noises was amplitude modulated. The predicted square-law function provided the best fit for four out of five observers. In a fourth task, one observer detected an interval of amplitude modulation in a continuous noise. As predicted by the theory, a fourth-power function provided the best fit. In addition, Weber fractions for difference discriminations decreased approximately with the square root of sample duration for durations up to 300 msec, whereas Weber fractions for increment detections decreased approximately directly with duration for durations up to 100 msec. The results are usually in qualitative agreement with the theory and often in quantitative agreement as well.     

Developmental changes in infants' sensitivity to octave-band noises

Localization responses to octave-band noises with center frequencies at 200, 400, 1000, 2000, 4000, and 10,000 Hz were obtained from infants 6, 12, and 18 months of age. During an experimental trial, an octave-band noise was presented on one of two speakers located 45° to each side of the infant. A head turn to the noise (correct response) was rewarded by activating an animated toy on top of the speaker. The intensity of the noise was varied over trials (method of constant stimuli) to determine thresholds at each center frequency. Thresholds for the lower frequencies were approximately 5–8 db higher in the 6-month-old infants compared to the older infants. However, there were no consistent differences among groups at the higher frequencies. Infant thresholds were found to be 20–30 db higher than adult thresholds at the lower frequencies. At the higher frequencies thresholds for infants were approaching those of adults.     

Loudness functions under inhibition

In both vision and hearing, a masking or inhibiting stimulus increases the slope (exponent) of the power function that relates sensation to stimulus. The power transformation applies only to the inhibited part of the function where the signal is fainter than the masking noise. Where the signal equals the noise, the function shows a discontinuous knee. Experiments were undertaken to see whether the loudness of a tone of 1000 Hz in a white noise would follow a model based on a constant signal-to-noise ratio at two locations, at the effective threshold and at the knee where the inhibited function meets the uninhibited function. The data accord with the slopes (exponents) generated by the model. The same model gives a fairly good account of the recruitment functions for ears suffering from cochlear involvement (e.g., Méniere’s disease). Regardless of degree of hearing loss, loudness recruitment reaches normal when the tone (1000 Hz) is about 30 dB above the affected threshold.     

Lateralization of narrow-band noise by blind and sighted listeners

The effects of varying interaural time delay (ITD) and interaural intensity difference (IID) were measured in normal-hearing sighted and congenitally blind subjects as a function of eleven frequencies and at sound pressure levels of 70 and 90 dB, and at a sensation level of 25 dB (sensation level refers to the pressure level of the sound above its threshold for the individual subject). Using an 'acoustic' pointing paradigm, the subject varied the IID of a 500 Hz narrow-band (100 Hz) noise (the 'pointer') to coincide with the apparent lateral position of a 'target' ITD stimulus. ITDs of 0, +/-200, and +/-400 micros were obtained through total waveform delays of narrow-band noise, including envelope and fine structure. For both groups, the results of this experiment confirm the traditional view of binaural hearing for like stimuli: non-zero ITDs produce little perceived lateral displacement away from 0 IID at frequencies above 1250 Hz. To the extent that greater magnitude of lateralization for a given ITD, presentation level, and center frequency can be equated with superior localization abilities, blind listeners appear at least comparable and even somewhat better than sighted subjects, especially when attending to signals in the periphery. The present findings suggest that blind listeners are fully able to utilize the cues for spatial hearing, and that vision is not a mandatory prerequisite for the calibration of human spatial hearing.     

Low-noise microvolt level calibrator for measurement of performance of biosignal recording systems

A calibrator, the noise level of which is below the noise level generated in the preamplifier system, was needed for testing and development of a multichannel recording system. A multichannel preamplifier head assembly was used for recording cortical, subcortical, and cerebellar slow potentials and multiunit activity in freely moving cats and restrained rabbits. An inexpensive, battery-powered, lownoise voltage signal generator for calibration of the preamplifiers is described. The circuit provides a square-wave output at a frequency of 10 or 1000 Hz, and the peak-to-peak (p-p) amplitude can be selected at 10, 100, or 1000µV. The measured output noise of the calibrator is below 2µV (p-p, 0.1–6000 Hz). The frequency and amplitude values can be easily adapted for different purposes by changing a few component values. An amplified (gain 1,000×) test output for direct oscilloscope monitoring is included in the calibrator circuit.     

Effects of noise on pure-tone thresholds in blackbirds (Agelaius phoeniceus and Molothrus ater) and pigeons (Columba livia)

Blackbirds and pigeons were trained to detect tones in quiet and in broadband noise by using positive-reinforcement techniques. In Experiment 1, thresholds in noise were obtained in blackbirds as a function of both tone frequency and noise intensity for a pulsed noise masker (noise gated on and off with tone). For blackbirds, critical ratios (the ratio of the power of the just-detectable tone in noise to the power of the noise masker) obtained in pulsed noise showed no consistent relation to tone frequency. For pigeons, on the other hand, critical ratios obtained in continuous noise increased by about 3 dB/octave across their range of hearing, being similar to known critical ratio functions for cats and humans. In Experiment 2, critical ratios in blackbirds obtained with both continuous noise and pulsed noise were compared. Blackbird critical ratios were more stable in continuous noise and averaged 4 dB lower than critical ratios in pulsed noise. The blackbird critical ratio function obtained with continuous noise was similar to the known critical ratio function of another avian species, the parakeet. Thus, small birds appear to have atypical critical ratio functions, compared with pigeons and other vertebrates.     

Effect of low-frequency random noises on performance of a numeric monitoring task.

Previous findings indicate that continuous low-frequency noises at moderate sound-pressure levels do not produce decrements in vigilance performance. Such noises are commonly found in urban environments, however; and it is important to explore their effects carefully. This study employed 27 human males in a numeric monitoring task to evaluate the effects of low-frequency (11.5 to 350 Hz) noise at moderate sound-pressure levels (80 db). More numeric signals were missed during noise than during control runs. The effect was small but statistically reliable (P smaller than .033), in disagreement with previous research. The possible environmental impact of these findings is discussed.     

Lateralization of an auditory signal in correlated noise and in uncorrelated noise as a function of signal frequency

Listeners lateralized a monaural signal presented against a continuous background of perfectly correlated noise (NO) or of uncorrelated noise (NU). Measures of signal detectability were also secured in separate tests. Psychometric functions (percent correct vs signal energy) were determined for each task. For a tonal signal of either low or high frequency, a listener requires only slightly greater signal energy (about 1 dB) in order to lateralize as well as he can detect when the noise is uncorrelated (NU). When the noise is perfectly correlated (NO), the slope of the psychometric function for lateralization depends upon signal frequency. With 250 Hz, the slope of the psychometric function for lateralization is much smaller than that for detection. With 1,000 Hz, the function for lateralization is steeper than that for 250 Hz, but the slope is still less than that of the function for detection for 1,000 Hz. With 2,000 Hz, the function for lateralization has about the same slope as that for detection.     

Frequency-selective detection at three signal amplitudes

Using the probe-signal method, frequency-response characteristics were obtained for four Os detecting signals nominally of only 1000Hz under three signal-amplitude conditions: E/N_o=10.0, 12.6, and 15.8. Detection of 1000-Hz signals decreased systematically with signal-amplitude decreases, but signals at 850 Hz and at 1150 Hz were detected at or near the chance level during all signal-amplitude conditions. From the detection performance data, the detectability was inferred for four probe-signal frequencies relative to that of 1000-Hz signals for each of the amplitude conditions. From the curvesofrelative detectability, hal[-detectability bandwidths were estimated. Neither the relative detectability curves nor the half-detectability bandwidths indicate any systematic change in the frequencyselectivebehavior of the auditory O across the signal amplitudes used.     

不同背景音对中文篇章阅读影响的眼动研究

采用眼动记录技术,考察不同背景音对中文篇章阅读和词汇加工的影响。结果发现：（1）与安静和白噪音背景相比,无关言语背景下的总阅读时间更长、阅读速度更慢、注视次数更多、平均眼跳幅度更小。（2）不同背景音下的首次注视时间和凝视时间无显著差异,而无关言语背景下的回视路径时间和总注视时间较白噪音条件下的更长。结果表明,无关言语干扰了读者的阅读过程,其语义成分和声学特征变化是干扰产生的重要原因;这种干扰体现在词汇加工中的语义整合阶段。     

On theoretical and realizable ideal conditions in psychophysics: Magnitude and category scales and their relation

By spacing 10 stimuli (white noise) between 40 and 110 dB according to two criteria [equal response ambiguity (ERA) and equal discriminability (ED)], an attempt was made to construct an “ideal” case for magnitude estimation and category rating. The “ideal” case is defined by linear and constant Weber functions (SDs as a function of scale values) for the two scales, respectively. Altogether, three group and two individual magnitude and category rating experiments were run with these two spacings. It was found that the ERA spacing approximated the ideal case well for both Weber functions and the ED spacing only for the Weber function of the category scale. The general psychophysical differential equation that relates scale values and Weber functions for the two scales allowed good prediction of the category scales from the magnitude scales and the Weber functions. The data suggested a distinction between phenotypic (empirical) and genotypic Weber functions, analogous to “real” and “ideal” cases in physics.     

Contrast masking reveals spatial-frequency channels in stereopsis.

Yang and Blake (1991 Vision Research 31 1177-1189) investigated depth detection in stereograms containing spatially narrow-band signal and noise energies. The resulting masking functions led them to conclude that stereo vision was subserved by only two channels peaking at 3 and 5 cycles deg-1. Glennerster and Parker (1997 Vision Research 37 2143-2152) re-analysed these data, taking into account the relative attenuation of low- and high-frequency noise masks as a consequence of the modulation transfer function (MTF) of the early visual system. They transformed the data using an estimated MTF and found that peak masking was always at the signal frequency across a 2.8 octave range. Here we determine the MTF of the early visual system for individual subjects by measuring contrast thresholds in a 2AFC orientation-discrimination task (horizontal vs vertical) using band-limited stimuli presented in a 7 deg x 7 deg window at 4 deg eccentricity. The filtered stimuli had a bandwidth of 1.5 octaves in frequency and 15 degrees in orientation at half-height. In the subsequent stereo experiment, the same (vertical) filters were used to generate both signal and noise bands. The noise was binocularly uncorrelated and scaled by each subject's MTF. Subjects performed a 2AFC depth-discrimination task (crossed vs uncrossed disparity) to determine threshold signal contrast as a function of signal and mask frequency. The resulting functions showed that peak masking was at the signal frequency over the three octave range tested (0.4-3.2 cycles deg-1). Comparison with simple luminance-masking data from experiments with similar stimuli shows that bandwidths for stereo masking are considerably larger. These data suggest that there are multiple bandpass channels feeding into stereopsis but that their characteristics differ from luminance channels in pattern vision.     

Masking of motion by broadband and filtered directional noise

Observers detected unidirectional motion of isotropic dotpatterns following exposure to (1) broadband noise containing all directions of motion, or (2) noise from which certain sets of direction had been filtered. The amount of maskingvaried withtheset of directions filtered from the noise, yielding broad directional tuning functions. The breadth of an observers’s tuning function corresponded to the precision with which the observer could recognize small differences in direction of motion.     

Detection of auditory signals presented at random times

One hundred msec tones of 1000 Hz at four intensities were presented according to two Poisson schedules in a background of wide band noise and as increments to a 1000 Hz tone. Each 15 minute test session was run under fixed conditions and one of three instructions to detect the signals; the two Ss were free to respond at any time. The data analyzed were several inter-response and signal-response distributions, and they were compared with a theory due to Luce. Discrepancies between the theory and data indicate needed modifications of both the theory and the procedure.     

Effect of simultaneous auditory stimulation on vibrotactile thresholds

Vibrotactile thresholds were determined at 250 and 400 Hz in the presence of (1) the sounds emitted by the vibrator, (2) continuous tonal or narrow-band masking noise, or (3) a pulsed tone synchronized with the vibrator signal. The measure of a cross-modality effect was the threshold shift occurring between each condition and the control condition, in which earmuff silencers eliminated the vibrator sounds. Continuous tones or noise had no effect upon vibrotactile thresholds. However, auditory signals synchronized with the vibrator signals did significantly elevate vibrotactile thresholds.     

Observer weighting of interaural delays in filtered impulses

Onset dominance in sound localization was examined by estimating observer weighting of interaural delays for each click of a train of high-frequency filtered clicks. The interaural delay of each click was a normal deviate that was sampled independently on each trial of a single-interval design. In Experiment 1, observer weights were derived for trains ofn=2, 4, 8, or 16 clicks as a function of interclick interval (ICI=1.8, 3.0, or 12.0 msec). For smalln and short ICI (1.8 msec), the ratio of onset weight to remaining weights was as large as 10. As ICI increased, the relative onset weight was reduced. For largen and all ICIs, the ongoing train was weighted more heavily than the onset. This diminishing relative onset weight with increasing ICI andn is consistent with optimum distribution of weights among components. Efficiency of weight distribution is near ideal when ICI=12 msec andn=2 and very poor for shorter ICIs and larger ns. Further experiments showed that: (1) onset dominance involves both within- and between-frequency-channel mechanisms, and (2) the stimulus configuration (ICI,n, frequency content, and temporal gaps) affects weighting functions in a complex way not explained by cross-correlation analysis or contralateral inhibition (Lindemann, 1986a, 1986b).