The roles of vibration amplitude and static force

Previous work (Verrillo, 1963, 1968) has shown that when measured as a change in absolute threshold, spatial summation occurs only at vibration frequencies above 40 Hz. The present study measured vibrotactile spatial summation at suprathreshold amplitudes. A matching task was used to investigate the effect of varying contactor size on sensory magnitude at three different vibration frequencies. Unlike the threshold data, increasing contactor size resulted in increases in sensory magnitude at 25 and 40 Hz as well as at 160 Hz. The amount of summation varied directly with amplitude for the two lower frequencies. In a second experiment, the effect of increasing static force, independent of contactor size, was investigated. The results indicated that the spatial summation effects noted in the first experiment may be due to increases in static force and not contactor area. The implications of these results for the concept of spatial summation and for the duplex mechanoreceptor hypothesis are discussed.     

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.     

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.     

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.     

Vibrotactile temporal summation for threshold and suprathreshold levels of stimulation

Threshold measurement and matching procedures were used to determine the amount of temporal summation at threshold and suprathreshold levels of vibrotactile stimulation on the thenar eminence of the hand. The frequency of the stimulus was 25, 40, 80, or 200 Hz. At 25 Hz, temporal summation was absent at all intensity levels. Considerable amounts of temporal summation were observed for 80- and 200-Hz stimuli, although the effects decreased as a function of intensity. At 40 Hz, no temporal summation was observed at threshold, but above threshold, a small amount was observed at all intensity levels. The results support a duplex model of mechanoreception in which one of two receptor systems exhibits temporal summation.     

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.     

Signal detectability in the presence of monotic or dichotic noise bands of equal or unequal levels

The application of the power-spectrum model of masking to the detectability of a signal masked by dichotic noise was investigated in three experiments. In each experiment, the signal was a 2-kHz sinusoid of 400-msec duration, masked by either one or two 800-Hz wide bands of noise presented singly or in pairs. In Experiment 1, we compared the detectability of a diotic signal masked by dichotic noise with the detectability of a monaural signal masked by each of the noises separately. The spectrum level of the noise was 35 dB SPL. For dichotic presentations, the signal was sent to both ears while pairs of noise bands, one below and one above the signal frequency, were presented together, one band to each ear. Threshold levels with the dichotic stimuli were lower than or equal to the thresholds with either ear's stimulus on its own. Similar dichotic stimuli were used in Experiment 2, except that the signal frequency was nearer to one or the other of the bands of masking noise, and the noise had a spectrum level of 50 dB SPL. In Experiment 3, thresholds were obtained with two sets of symmetrically and asymmetrically placed notched-noise maskers. For one of these sets, the spectrum level of both noise bands was 35 dB SPL; for the other set, interaural intensity differences were introduced in the form of an inequality in the levels of the noise bands on either side of the signal. In one ear, the spectrum level of the lower frequency noise band was 35 dB SPL and the spectrum level of the higher frequency noise band was 25 dB SPL, whereas in the other ear, the allocation of noise level to noise band was reversed. The dichotic thresholds obtained with the unequal noise maskers could be predicted from the shapes of the auditory filters derived with equal noise maskers. The data from all three experiments suggest that threshold signal levels in the presence of interaural differences in masker intensity depend principally on the ear with the higher signal-to-masker ratio at the output of its auditory filter, a finding consistent with the power-spectrum model of masking.     

Bilateral spatial summation of cooling of symmetrical sites

The possibility of spatial summation of conducted ??Ts (temperature decrements from the adapted skin temperature) was tested when the ??Ts were presented simultaneously and individually at symmetrical sites on either side of the body. The use of a signal detection rating method yielded data that indicate that spatial summation is complete (area and intensity trade reciprocally) for ??s near threshold and at clearly suprathreshold intensities of stimulation is invariant of the adapted skin temperature (AT), and the intensity of stimulation within the range of stimuli used (from as little as ?0.05?C to as much as ?1.25?C). In view of the characteristics ascribed to the thermosensory apparatus in humans, it is postulated that spatial summation occurs in the central nervous system.     

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 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.     

Transient and sustained masking

The detection threshold of a brief test stimulus was measured as a function of the onset asynchrony between it and a long-lasting suprathreshold masking stimulus. Both stimuli were sine-wave gratings of the same vertical orientation and in the peak-subtract phase but differed in spatial frequency by a factor of 3. The temporal masking functions obtained with 2- and 6-cycles/deg maskers of high contrast exhibited transient on- and off-peaks of masking and a sustained effect during the masker exposure. An 18-cycles/deg masker caused sustained masking only. Experiments with maskers of variable spatial frequency and contrast showed that, in the low-spatial-frequency range, the mechanism responsible for the transient effect was more sensitive than that generating the sustained effect, while the sustained effect required less contrast in the high-spatial-frequency range. The results are considered as evidence, in addition to previous findings, for the sustained/transient dichotomy in the temporal domain.     

Some nonmasking auditory postsignal effects

Observers were asked to detect a 20-msec segment of a sinusoidal signal masked by a band-limited white noise. A postsignal decrease in the spectrum level of the noise within the critical band of the signal enhanced the detectability of that signal if the decrease occurred within approximately 25 msec following signal termination. Postsignal decreases outside the critical band of the signal, and decreases within the critical band delayed longer than approximately 40 msec, reduced the detectability of the signal for decrease delays up to between approximately 150 and 400 msec, depending on the spectral characteristics of the decrease. Comparisons with typical backward masking results indicate probable common factors of short-term temporal summation and longer term attention.     

Binaural interaction in backward masking

The binaural auditory system exhibits certain advantages over the monaural system when detecting a tonal signal in a background of masking noise. These advantages have been described in detail and are referred to as masking-level differences, or MLDs. It has been demonstrated, for example, that performance in detecting a tonal signal that has been reversed in phase at one ear relative to the other ear is about 15–17 dB better than detection of the same signal in-phase at the two ears when masked by moderately intense masking noise that is in-phase at the two ears. The explanations for this phenomenon fall into two general categories, and both types of explanations are based upon the interaction of the tonal signal and masker when they are added together. In the present paper, data are presented which indicate that an MLD of at least 4–5 dB can be obtained in a binaural masking experiment in which the offset of the tonal signal precedes the onset of the noise masker.     

Independent detectors for expansion and rotation, and for orthogonal components of deformation.

It is well known that optic flow--the smooth transformation of the retinal image experienced by a moving observer--contains valuable information about the three-dimensional layout of the environment. From psychophysical and neurophysiological experiments, specialised mechanisms responsive to components of optic flow (sometimes called complex motion) such as expansion and rotation have been inferred. However, it remains unclear (a) whether the visual system has mechanisms for processing the component of deformation and (b) whether there are multiple mechanisms that function independently from each other. Here, we investigate these issues using random-dot patterns and a forced-choice subthreshold summation technique. In experiment 1, we manipulated the size of a test region that was permitted to contain signal and found substantial spatial summation for signal components of translation, expansion, rotation, and deformation embedded in noise. In experiment 2, little or no summation was found for the superposition of orthogonal pairs of complex motion patterns (eg expansion and rotation), consistent with probability summation between pairs of independent detectors. Our results suggest that optic-flow components are detected by mechanisms that are specialised for particular patterns of complex motion.     

Limulus psychophysics: Increment threshold

Prior temporal summation work had indicated that the sensory code for certain behaviors (in bothLimulus and humans) can be understood if one suggests that the central nervous system analyzes the integral of the photoreceptor potential. An independent test of this suggestion is available because (inLimulus) the physiological increment threshold function obtained from the receptor potential integral is inflected, whereas that obtained from the initial transient peak of the receptor potential is not. The behavioral increment threshold function was measured inLimulus and found to be inflected. Fechner’s scaling assumption (that equally detectable stimulus increments are mediated by sensory signals of equal size) was supported by the fact that a theoretical function, which was calculated from the receptor integral intensity-response function by using Fechner’s scaling assumption, was able to fit the behavioral increment threshold function quite well. Furthermore, the variability of the behavioral data was proportional to the receptor integral variability. A seasonal effect was observed: Fall animals were more sensitive and had a higher criterion than winter animals. These findings permit the specification of the rerceptor potential that mediates this particular behavior at threshold: It has a steady-state amplitude of 7 mV in winter and 16 mV in fall. Taken in conjunction with the results of earlier temporal summation work indicating that the threshold receptor potential is 4.5 sec long, this specification implies that at least some behaviors are mediated by large, long sensory signals, which have properties very different from those of small, short signals, particularly with regard to both linearity and their relative dependence on time vs. energy.     

The joint effect of forward and backward visual masking: Some comments on Uttal’s “Character in the hole” experiment

The joint effect of forward and backward visual masking appears to be more extended in time than that predicted from an algebraic summation of individual forward and backward masking effects. It is suggested that this apparent extension of the temporal range of masking arises from the summation of forward and backward masking effects which in themselves are insufficient to influence observed performance. Such latent masking effects are possible if it is not assumed that when stimulus identification reaches the 100% level the mask has no effect at all on the stimulus.     

Behavioral and electrophysiological measures of click audibility compared in the cat

Cats were trained to make an avoidance response to clicks in the presence of different levels of white masking noise. The audibility of the clicks at different masking intensities could be determined from the percentage of CRs made by the animals. Click-evoked responses were also recorded from the left inferior colliculus of each cat in the presence of several intensities of masking noise. The results showed that the noise level that just obscured the click-evoked response was quite close in intensity to the noise level that produced threshold click detection in the behavioral situation. While both behavioral and electrophysiological methods yielded similar measures of auditory sensitivity, the electrophysiological measure was obtained in a fraction of the time required to obtain the behavioral measure.     

Spatial summation of chemical irritation and itch produced by topical application of capsaicin

The effect of increasing the total area of stimulation on the sensations of irritation produced by topical application of capsaicin was studied in two experiments. In the first experiment, stimulus area was varied by changing the size of filter paper disks on which capsaicin was delivered to the skin of the forearm. Subjects rated the intensity and quality of the cutaneous sensations over a 15-min period. Increasing stimulus area by a factor of 15 resulted in a relatively modest increase in the peak perceived intensity of irritation, a shortening of the latency to the onset of irritation, and shifts in the frequency of reports of sensations of itching and stinging/pricking. However, itch was the most frequently reported sensation regardless of stimulus size. In Experiment 2, stimulus area was manipulated by varying the number of stimuli applied to the skin. Despite a smaller difference in total stimulus areas (9-fold vs. 15-fold), the difference in perceived irritation was more pronounced than it was in Experiment 1 and reached statistical significance. It is therefore concluded that spatial summation does occur in the afferent system or systems responsible for the perception of capsaicin on the skin. This result is consistent with previous reports of summation at the threshold for heat pain and constitutes new information about the spatial integration of pruritic stimulation.     

Binocular unmasking with unequal interocular contrast: The case for multiple Cyclopean eyes

Under certain conditions, the detection threshold for a sinusoidal grating embedded in a noisy background may be an order of magnitude lower when binocular cues are available than when monocular cues only are present. Such binocular unmasking occurs only when the degree of interocular disparity for the target differs from that of the background. Two classes of models have been advanced to account for such unmasking. The first assumes that orientation-specific, spatial frequency channels in each eye encode the amplitude and phase of the spatial frequency component of the pattern the channel is tuned to detect. Thus, a difference in interocular disparity between target and background could result in interocular amplitude and/or phase differences in left- and right-eye spatial frequency channels. When, however, there are no disparity differences between target and background, there will be no interocular differences in amplitude and phase in the left- and right-eye channels. In this model, then, binocular unmasking reflects the binocular system’s ability to respond to interocular amplitude and/or phase differences in the patterns presented to the two eyes. In the second class of models, it is assumed that the left and right-eye patterns are first summed to form a “Cyclopean” eye. In these models, detection depends on the effect this summation process has on the power spectrum of the summated patterns. To decide between these two classes of models, we observed the occurrence of binocular unmasking when (1) the contrast of masker and signal was varied identically in both eyes and (2) the contrast of masker and signal was varied in one eye only. Consistent with our previous research, we found that the results can be accounted for in terms of a linear summation model of binocular unmasking; the alternative interocular phase detection model was disproved. The implications of these findings for binocular contrast summation in the absence of visual noise are discussed.     

Spatial and temporal factors in masking by edges and disks

Increment threshold of a small test probe is found to be elevated by backgrounds of a disk, bar, or luminance step. The spatial parameters that produce maximum masking are found to be essentially similar with the three types of background. The lime course of masking is also found to be similar for the disk and bar background. It is suggested that a fundamentally similar type of visual processing underlies each of the masking situations.