The effect of white-noise mask level on sinewave contrast detection thresholds and the critical-band-masking model

It is known that visual noise added to sinusoidal gratings changes the typical U-shaped threshold curve which becomes flat in log-log scale for frequencies below 10c/deg when gratings are masked with white noise of high power spectral density level. These results have been explained using the critical-band-masking (CBM) model by supposing a visual filter-bank of constant relative bandwidth. However, some psychophysical and biological data support the idea of variable octave bandwidth. The CBM model has been used here to explain the progressive change of threshold curves with the noise mask level and to estimate the bandwidth of visual filters. Bayesian staircases were used in a 2IFC paradigm to measure contrast thresholds of horizontal sinusoidal gratings (0.25-8 c/deg) within a fixed Gaussian window and masked with one-dimensional, static, broadband white noise with each of five power density levels. Raw data showed that the contrast threshold curve progressively shifts upward and flattens out as the mask noise level increases. Theoretical thresholds from the CBM model were fitted simultaneously to the data at all five noise levels using visual filters with log-Gaussian gain functions. If we assume a fixed-channel detection model, the best fit was obtained when the octave bandwidth of visual filters decreases as a function of peak spatial frequency.     

Effect of ramp-like contours upon perceived size and detection threshold

Perceived widths and detection thresholds were measured for foveally viewed stimuli which were edged on two sides by luminance ramps. Perceived width approximated the distance between the midpoints of the ramps. It varied with the width of the ramps, but was unaffected by a five-fold change in the luminance of the stimulus. The detection threshold was higher for a ramp stimulus than for a normal stimulus of the same apparent width. The relationship between perceived width and detectability is consistent with a theoretical treatment based upon receptive-field mechanisms.     

Hearing and vocalizations in the orange-fronted conure (Aratinga canicularis)

The auditory sensitivities of the orange-fronted conure (Aratinga canicularis) were examined in relation to the spectral characteristics of its vocalizations. Absolute thresholds, masked thresholds, frequency difference limens, and intensity difference limens for pure tones were obtained using psychoacoustic techniques. In general, hearing abilities are similar to those found in many avian auditory generalists. One exception is the unusually low critical ratio (masked threshold) between 2.0 and 4.0 kHz, similar to that previously found in the budgerigar (Melopsittacus undulatus). These auditory sensitivities were compared with average spectra for (a) contact calls and (b) a general sample of vocalizations recorded from wild birds. The spectral regions of both greatest vocal energy and best auditory sensitivity were between 2.0 and 5.0 kHz.     

Effect of masker level on infants' detection of tones in noise

In adult listeners, the signal-to-noise ratio at masked threshold remains constant with increases in masker level over a wide range of stimulus conditions. This relationship was examined in 7-month-old infants by obtaining masked thresholds for .5- and 4-kHz tones presented in four levels of continuous masking noise. Adults were also tested for comparison. Masker spectrum levels ranged from 5 to 35 dB/Hz for .5-kHz tones, and from -5 to 25 dB/Hz for 4-kHz stimuli. Thresholds were determined for stimuli of both 10 and 100 msec in duration. The results indicated that infants' performance was more adult-like for 4-kHz stimuli. Although mean thresholds for both 10- and 100-msec, 4-kHz tones were approximately 7 dB higher in infants than in adults, E/N0 at threshold remained essentially constant over the 30-dB range of maskers employed. By contrast, infants' thresholds for .5-kHz tones were exceptionally high at lower levels of the masker. Threshold E/N0 decreased significantly as masker level increased from 5 to 35 dB/Hz, and this decrease was significantly greater for 10- than for 100-msec stimuli. Temporal summation of .5-kHz tones, measured as the difference between thresholds obtained at the two signal durations, was greater for infants than for adults at low levels of the masker. However, because infants' thresholds improved more rapidly with level for 10- than for 100-msec tones, age differences in temporal summation were no longer significant when masker spectrum level was 35 dB/Hz. These results suggest that the relationship between signal-to-noise ratio at masked threshold and level of the masker is dependent on both signal frequency and duration during infancy.     

Effect of masker level on infants’ detection of tones in noise

In adult listeners, the signal-to-noise ratio at masked threshold remains constant with increases in masker level over a wide range of stimulus conditions. This relationship was examined in 7-month-old infants by obtaining masked thresholds for .5- and 4-kHz tones presented in four levels of continuous masking noise. Adults were also tested for comparison. Masker spectrum levels ranged from 5 to 35 dB/Hz for .5-kHz tones, and from ?5 to 25 dB/Hz for 4-kHz stimuli. Thresholds were determined for stimuli of both 10 and 100 msec in duration. The results indicated that infants’ performance was more adultlike for 4-kHz stimuli. Although mean thresholds for both 10- and 100-msec, 4-kHz tones were approximately 7 dB higher in infants than in adults, E/N₀ at threshold remained essentially constant over the 30-dB range of maskers employed. By contrast, infants’ thresholds for .5-kHz tones were exceptionally high at lower levels of the masker. Threshold E/N0 decreased significantly as masker level increased from 5 to 35 dB/Hz, and this decrease was significantly greater for 10- than for 100-msec stimuli. Temporal summation of .5-kHz tones, measured as the difference between thresholds obtained at the two signal durations, was greater for infants than for adults at low levels of the masker. However, because infants’ thresholds improved more rapidly with level for 10- than for 100-msec tones, age differences in temporal summation were no longer significant when masker spectrum level was 35 dB/Hz. These results suggest that the relationship between signal-to-noise ratio at masked threshold and level of the masker is dependent on both signal frequency and duration during infancy.     

Detection by the guinea pig of acoustic stimulation and of electrical stimulation of the brain

A threshold procedure using operant behavioral techniques with positive reinforcement was developed after initial efforts with avoidance behavioral procedures proved unsatisfactory. In the first of three experiments the operant threshold procedure was tested by determining masked auditory thresholds for trains of clicks. In a second experiment, similar techniques were used to measure thresholds for electrical stimulation of the brain. The last experiment, again an auditory problem, involved a determination of the absolute thresholds for trains of short noise bursts as a function of the time between bursts. Middle ear malfunction proved to be a more severe problem than had been anticipated on the basis of reports in the literature. The threshold procedure, however, seems to be adequate for determination of absolute or masked thresholds with auditory or electrical stimuli.     

Frequency selectivity for hearing-impaired and broadband-noise-masked normal listeners

When evaluating frequency selectivity, it is difficult to determine if the deviation from normal performance observed for hearing-impaired listeners reflects abnormal cochlear function or normal, level-dependent changes in frequency selectivity. This experiment was designed to investigate the dependence of frequency-selectivity measures on threshold and signal level. Auditory-filter characteristics, critical ratios, forward-masked psychophysical tuning curves, and narrowband-noise masking patterns were obtained from normal-hearing listeners in quiet and in the presence of broadband noise at five levels. These findings were then compared to previously obtained frequency-selectivity measurements for subjects with mild-to-moderate sensorineural hearing loss whose absolute thresholds are comparable to the normal-hearing listeners' masked thresholds. The results suggest that frequency selectivity deterioriates as threshold increases for all subjects. However, the poor frequency selectivity exhibited by hearing-impaired listeners may not be explained entirely by the effects of threshold and signal level. Nevertheless, because frequency selectivity is poorer in the normal auditory system at higher stimulus levels, the deviation from normal performance observed for hearing-impaired listeners may not be as large as previously suggested.     

Frequency selectivity using tonal-temporal masking: Diotic vs. dichotic masking

A combined forward-backward masking procedure was used to investigate the threshold of a 30-msec, 500-Hz signal as a function of masker frequency. The signal thresholds were obtained in two signal conditions, diotic (So) and dichotic (S_π), and for two different temporal separations of the maskers. The maskers were 500 msec in duration and were presented at 75 dB SPL. The function relating masked signal threshold to masker frequency was used to describe frequency selectivity in the four conditions. There were no differences in frequency selectivity measured between the diotic and dichotic signal conditions and only a small difference measured between the two intermasker interval conditions. The S_π conditions yielded lower thresholds than did the So conditions. The change in intermasker interval from 10 to 50 msec lowered the threshold maximally 18 dB for the So condition and 13 dB for the S_π condition. The results indicate that in this tonal temporal masking procedure there are no differences between the diotic and dichotic critical bands.     

Sex differences in pain and thermal sensitivity: the role of body size

Sex differences in heat-pain and thermal sensitivity were investigated in 32 women (20 to 60 years of age) and 32 men (17 to 63 years of age) who had no somatosensory impairments. Pain thresholds were measured with stimuli of two different durations (phasic and tonic). Warmth and cold thresholds were assessed as indices of thermal sensitivity. Stimulation was applied to the hand and to the foot by an apparatus containing a Peltier thermode. There were no sex differences in heat-pain thresholds. Women had significantly lower warmth thresholds than men (more pronounced on the foot than on the hand), but similar cold thresholds. Measures of body size (weight, height) correlated much more strongly with thermal than with pain sensitivity, and helped to explain the sex difference in the warmth threshold. A reduction of sex differences to body-measure differences appears likely, but could not be demonstrated unequivocally.     

Binocular detection of masked patterns in young and old observers

A visual pattern embedded in noise is detected appreciably better when the stimulus complex contains interocular cues (dichoptic condition) than when such cues are absent (binoptic condition). In a recent study (F. Speranza, G. Moraglia, & B. A. Schneider, 1995) the authors showed that the relative difference between binoptic and dichoptic thresholds does not change with age. However, older adults showed higher binoptic and dichoptic thresholds, thus suggesting an age-related difficulty with degraded stimulation. In this article the authors first replicated these findings and proceeded next to investigating whether age-related changes in processing efficiency, additive internal noise, and the spatial frequency bandwidth of the detecting filters could account, separately or concurrently, for the elevated thresholds in noise exhibited by the older adults. Results indicate that this increase is not attributable to age-related changes in filter bandwidth or internal noise. Rather, the findings can be explained in terms of a decrease in processing efficiency with age.     

Developmental changes during childhood in single-letter acuity and its crowding by surrounding contours

Crowding refers to impaired target recognition caused by surrounding contours. We investigated the development of crowding in central vision by comparing single-letter and crowding thresholds in groups of 5-year-olds, 8-year-olds, 11-year-olds, and adults. The task was to discriminate the orientation of a Sloan letter E. Single-letter thresholds, defined as the stroke width forming the smallest discriminable E, were worse than those of adults (0.83 arcmin) at 5 years of age (1.05 arcmin) but not at older ages (8-year-olds: 0.81 arcmin; 11-year-olds: 0.78 arcmin). The maximum distances over which crowding occurred, as measured in multiples of threshold stroke width, were smaller in adults (2.83) than in the three groups of children, who did not differ from each other (5-year-olds: 7.03; 8-year-olds: 7.84; 11-year-olds: 7.13). Thus, even 11-year-olds are more affected than adults by surrounding contours despite having single-letter acuity that has been mature for several years. The stronger influence of crowding in children may be caused by immaturities in the brain areas beyond the primary visual cortex (V1) where early visual inputs are combined and may contribute to their slower reading speed.     

Asymmetry of masking between noise and tone

A pure tone was used to mask narrow and wide bands of noise centered on the frequency of the tone. In a given experimental session, the sound-pressure level (SPL) of the tone was held constant and loudness balances were obtained between a masked and unmasked noise band of equal width. These results are compared to earlier measures of the partial masking of tone by noise. The comparison shows that noise masks a tone more effectively than the tone masks the noise. Although the effect of the tone on a critical band of noise is greater than its effect on either an octave-band noise or wide-band noise, it is considerably smaller than the effect of the noise on the tone. Decreasing the noise bandwidth still further to a subcritical width reduces the asymmetry of masking somewhat, but a difference at high intensities of about 20 dB between the masking effects of an equally intense noise and tone remains. Whether the masker is a tone or noise, masking ceases when the effective energy of the masked and masking stimuli is the same.     

Hearing in passerine and psittacine birds: a comparative study of absolute and masked auditory thresholds

Operant conditioning and a psychophysical tracking procedure were used to measure auditory thresholds for pure tones in quiet and in noise for seven species of small birds--the budgerigar, canary, cockatiel, European starling, song sparrow, swamp sparrow, and the zebra finch. Audibility curves are roughly similar among the seven birds, with the maximum sensitivity between 2 and 5 kHz and poorer sensitivity outside this narrow region. Critical ratios (signal-to-noise ratio at masked threshold) were calculated from pure-tone thresholds in noise. Except for the budgerigar, the critical ratio functions of all birds increase at the rate of 3 dB/octave. This pattern is typical of that observed in most vertebrates. Critical ratios in the budgerigar, on the other hand, decrease gradually from 0.5 kHz to 2.8 kHz and increase dramatically above 2.8 kHz. The present research demonstrates that the critical ratio function for the budgerigar is not only different from other vertebrates but also different from other birds.     

Motion perception in the ageing visual system: minimum motion, motion coherence, and speed discrimination thresholds

We aimed to address two issues: first, to describe how the perception of motion differs in elderly observers as compared to younger ones; and, second, to see if these changes in motion perception could be accounted for by the known changes in the ability of elderly observers to detect patterns (as indexed via contrast sensitivity). The lower threshold of motion, motion coherence, and speed discrimination were measured, alongside contrast sensitivity, in a group of thirty-two older (mean age 61.5 years) and thirty-two younger (mean age 23.2 years) subjects. The older observers showed losses in their ability to detect slow motions as indexed via the lower threshold of motion for random-dot patterns and for gratings of a range of spatial frequencies. They also were impaired on a test of motion coherence, but only for stimuli of a slow to medium speed, whereas faster speeds showed no decline with age. Finally, at all speeds tested the older observers required greater differences in speed in order to discriminate between patterns moving at different speeds. The pattern of losses on motion perception tasks was not predicted by the deficits of the older groups, such as loss of detection thresholds for high spatial and/or temporal frequencies. It is concluded that these hypotheses do not provide an adequate account of the data, and therefore that the losses occurring with age are complex and probably are a result of the loss of several types of cell.     

Tactile sensitivity of children: effects of frequency, masking, and the non-Pacinian I psychophysical channel

Tactile perception depends on the contributions of four psychophysical tactile channels mediated by four corresponding receptor systems. The sensitivity of the tactile channels is determined by detection thresholds that vary as a function of the stimulus frequency. It has been widely reported that tactile thresholds increase (i.e., sensitivity decreases) as a function of age. However, there is controversial evidence with regard to the progressive loss of sensitivity starting from childhood. In this study, the tactile thresholds of children (n=9, ages 7-11 years) were measured and compared with the thresholds of young adults (n=11, ages 21-27 years). The stimuli consisted of sinusoidal bursts of mechanical displacements, which were applied to the left index fingertips of the participants by using a cylindrical probe (base area=0.126 cm2) without a contactor surround. Absolute thresholds were measured at frequencies of 2, 10, 40, 100, 250, and 500 Hz without masking. The absolute thresholds decreased at high frequencies and were similar to data from the literature except for some discrepancy because of methodological differences. In addition, the threshold of the non-Pacinian I channel was measured at 40 Hz by elevating the thresholds of the Pacinian channel by forward masking. The effects of forward masking in children were similar to results in young adults. In conclusion, there were no significant differences between the tactile thresholds of children and those of young adults at key frequencies: 40 Hz for the Pacinian and non-Pacinian I channels and 250 Hz for the Pacinian channel. These findings contradict the hypothesis that there is gradual loss of tactile sensitivity starting from childhood to early adulthood. The loss of sensitivity due to aging probably is more abrupt and occurs at a later age.     

A comparison of thresholds for 1/3-octave filtered clicks and noise bursts in infants and adults

Behavioral thresholds of 6-month-old infants and adults were determined for 1/3-octave filtered clicks and 300-msec noise bursts with center frequencies ranging from .5 to 8 kHz. For noise bursts, differences between infant and adult thresholds were largest at low frequencies and smallest at 8 kHz. For clicks, infants’ thresholds were most like adults’ at 4 kHz, and age differences increased at both lower and higher frequencies. Differences between click and noise thresholds were significantly larger for infants than for adults at .5, 1, and 8 kHz, but not at 2 and 4 kHz. These results suggest that improvements in threshold for long-duration stimuli during infancy may not be accompanied by comparable changes in threshold at short durations. The delayed development of sensitivity to low- and high-frequency clicks appears consistent with maturational trends recently described for the auditory brainstem response.     

Musical duplex perception: perception of figurally good chords with subliminal distinguishing tones.

In a variant of duplex perception with speech, phoneme perception is maintained when distinguishing components are presented below intensities required for separate detection, forming the basis for the claim that a phonetic module takes precedence over nonspeech processing. This finding is replicated with music chords (C major and minor) created by mixing a piano fifth with a sinusoidal distinguishing tone (E or E flat). Individual threshold intensities for detecting E or E flat in the context of the fixed piano tones are established. Chord discrimination thresholds defined by distinguishing tone intensity were determined. Experiment 2 verified masked detection thresholds and subliminal chord identification for experienced musicians. Accurate chord perception was maintained at distinguishing tone intensities nearly 20 dB below the threshold for separate detection. Speech and music findings are argued to demonstrate general perceptual principles.     

An Examination of Sex and Masculinity/Femininity as Related to the Taste Sensitivity of Japanese Students

The purpose of the present study was to examine the influences of gender differences and masculinity–femininity on taste thresholds and food preferences. The participants were 108 Japanese undergraduate students (44 men and 64 women); their mean age was 19.6 years (SD = 1.3). Their detection and recognition thresholds for caffeine and sucrose were measured. Multiple regression analyses showed that women tended to have a lower detection threshold for caffeine than men did. The recognition threshold for caffeine was positively associated with scores for masculinity. For men, masculinity may be associated with smoking and drinking behavior, thereby resulting in a lower sensitivity for bitterness. Masculinity and femininity related to food preferences are also discussed.     

Detection of amplitude modulation and frequency modulation in tactual gratings: a critical bandwidth for active touch

Since most natural surfaces are complex and vary in amplitude and spatial frequency, it might be interesting to consider gratings not in the spatial domain, but in the spatial-frequency domain. Detection thresholds for amplitude modulation (AM) and frequency modulation (FM) in sinusoidal gratings were measured for seven participants. Participants moved their fingers actively across the gratings. Although the two types of modulation are quite different in the spatial domain, they have many features in common in the frequency domain. In previous research (Nefs et al 2001 Perception 30 1263-1274) we measured the discrimination thresholds for amplitude and frequency for sinusoidal gratings. We hypothesised then that these thresholds could be used to predict the discriminability of other types of gratings. In the present study, we did indeed find that the FM and AM detection thresholds can be understood quite well by these discrimination thresholds. The results indicate that the tactual system contains parallel psychophysical channels that filter and integrate the power of stimuli within critical bands. With these results, we are also able to calculate the critical bandwidth for active dynamic touch. We estimated the critical bandwidth surrounding the spatial frequency of 2 cycles cm(-1) to be about 125% of that spatial frequency. This value for the critical band for spatial frequency is incompatible with previous findings for temporal frequencies in vibrotactile research. This indicates that dynamic spatial-frequency discrimination is not likely to be done by temporal frequency.     

Olfactory sensitivity: reliability, generality, and association with aging.

Thirty-two Ss between 22 and 59 years of age yielded detection thresholds for 4 odorants over 4 sessions. The thresholds decreased and reliability increased over the course of testing. High intercorrelations between odorants and the stability of an S's relative position within the threshold distributions showed that a general factor of sensitivity dominated the outcome. Age contributed strongly to intersubject variation. Even among these nonelderly individuals, it accounted for up to 2 orders of magnitude in threshold performance. Other important factors included superiority of the right nostril and a negative correlation between the mean and variance of threshold distributions. Scant attention to the correlation may have contributed to overestimation of the frequency and specificity of specific anosmia. A clinically relevant outcome was that measurement of threshold for diagnostic purposes can generally rely on just 1 odorant.