Spatial-frequency-dependent visible persistence and specific reading disability

Visible persistence duration for sine-wave gratings was measured in 9-year-old normal and specific-reading-disabled children. Experiment 1 investigated the influence of stimulus duration on visible persistence. The results demonstrated a Reading Group X Spatial Frequency interaction with disabled readers showing a smaller increase in persistence duration with increasing spatial frequency than controls. This interaction was greatest with stimulus durations longer than 80 msec. In Experiments 2a and 2b persistence was measured across a range of contrasts from .1 to .5. The stimulus durations employed were 100 msec in Experiment 2a and 300 msec in Experiment 2b. In both experiments, increasing contrast decreased persistence duration at 2 and 12 cycles per degree (c/deg) for the control group. In the specific-reading-disabled group, however, contrast had little effect on the persistence of 2-c/deg gratings in either experiment. In Experiment 2a the persistence of the 12-c/deg grating decreased with increasing contrast for both groups. In Experiment 2b contrast had significantly less effect on persistence duration in the specific-reading-disabled group, however, contrast had little effect on the persistence of 2-c/deg ratings in either experiment. In Experiment 2b contrast had significantly less effect on persistence duration in the specific-reading-disabled group than in the control group at 12 c/deg. Consequently, contrast had less effect on persistence in specific-reading-disabled children than in normal readers, especially at durations longer than the "critical duration" for each spatial frequency. Experiment 3 extended this finding to gratings with spatial frequencies of 4 and 8 c/deg. These results indicate a difference between normal and specific-reading-disabled children in cortical visible persistence. Two scores of visual processing were derived from the above experiments. On these scores the reading-disabled children were divided into Visual Disabled Readers (approximately 70%--eight subjects) and Nonvisual Disabled Readers (approximately 30%--four subjects). The percentages of disabled readers in each category remained constant when the sample size was increased to 61 normal and disabled readers.     

Contrast constancy revisited: The perceived contrast of sinusoidal gratings above threshold

The contrast sensitivity function of the human visual system, measured with sinusoidal luminance gratings, has an inverted U shape with a peak around 2–4?c/deg. Above threshold, it is thought that luminance gratings of equal physical contrasts but of distinguishably different spatial frequencies are all perceived as having similar contrasts, a phenomenon that has been termed contrast constancy. However, when suprathreshold contrast matches were measured for pairs of luminance gratings whose spatial frequencies were indistinguishable, the matching curves were not flat and followed a similar inverted U shape form as the contrast sensitivity function at threshold. It was therefore suggested that contrast constancy may only be revealed when matching the contrasts of clearly distinguishable spatial frequencies. Here, observers matched the perceived contrasts of suprathreshold luminance gratings of similar but visibly different spatial frequencies between 0.25 and 16?c/deg. The results show that, much like the contrast sensitivity function at threshold, observers are more sensitive to intermediate spatial frequencies (1–6?c/deg) than they are to either higher or to lower spatial frequencies. This tuning is evident when matching reference contrasts of 30–80%, implying a significant role in everyday vision. To demonstrate that these results were not due to local adaptation, the experiment was repeated with shorter stimulus duration, producing the same results. The extent of departure from contrast constancy found in the present study is compared to previously reported suprathreshold measurements. The results are also discussed with consideration to limitations with display apparatus such as monitor blur.     

Simple reaction times to the onset,onset, and contrast reversal of sinusoidal grating stimuli

Response latencies to the onset, offset, and contrast reversal of sinusoidal gratings over a range of spatial frequencies were measured. For gratings of constant physical contrast, RT was monotonically related to spatial frequency regardless of presentation mode. Comparison of RTs to 1.0- and 9.0-cycle/deg gratings adjusted to equal apparent contrast showed that the RT shifts cannot be directly attributed to contrast sensitivity differences. It is concluded that spatial-frequency-dependent processing delays occur regardless of which temporal property of the stimulus the subject must respond to.     

The effects of adaptation to square-wave gratings as a function of grating orientation

An adaptation technique was used to measure the selectivity or tuning for grating orientation in the visual system for different orientations of the inspection stimulus. Duration thresholds for grating patterns of constant luminance were determined for 13 test gratings oriented from ±5 to 90 deg away from each of five adaptation gratings: 0, 22, 45, 67, and 90 deg. Threshold data obtained for test gratings without prior adaptation indicated higher sensitivity for gratings oriented along the horizontal and vertical axis than along the oblique axis. After adaptation, thresholds increased (sensitivity was reduced) for gratings having similar orientations as the test gratings. However, the functions relating sensitivity reduction to degree of angular disparity between test and adaptation grating did not vary across the five inpsection orientations, i.e., selectivity or tuning for grating orientation appeared to be independent of the orientation of the adapting stimulus.     

Left-right visual field asymmetry in bistable motion perception

Twelve observers viewed two alternating frames, each consisting of three rectangular bars which were displaced laterally by one cycle in one frame with respect to the other. At long interframe intervals (IFIs) observers perceived a group of three elements moving as a whole (group movement), whereas with IFIs shorter than 40-60 ms the overlapping elements in each frame appeared stationary while the third element appeared to move from one end of the display to the other (end-to-end movement). The percentage of group movement responses in central viewing was compared to those obtained for stimulus presentation in the left and right visual fields (4 deg eccentricity), for opposite horizontal directions of motion. All ten right-handed subjects showed a left-field advantage in sensitivity to group movement. The two left-handed subjects showed a similar advantage in sensitivity with right-field presentation. The effects of monocular vision, hand used in the task, spatial frequency, and contrast on visual field asymmetry were all investigated in two right-handed subjects. None of these factors affected the left-right asymmetry.     

Spatial-frequency uncertainty and cuing effects on psychometric functions for contrast detection

In the present study, the effects of spatial-frequency uncertainty and cuing on psychometric functions for contrast detection of sinusoidal gratings are examined. For this purpose, psychometric functions were collected from 4 subjects under fixed-frequency, randomized-frequency, and cued-frequency conditions. The experiment was conducted with a temporal two-alternative forced-choice task, and five spatial frequencies in the range of 0.5 and 8.0 c/deg and seven contrast levels for each frequency were used. The results showed that the psychometric functions for the randomized-frequency condition were shallower than those for the fixed-frequency condition, supporting the single-band model for the uncertainty effects (Hübner, 1993a, 1993b). For the cued-frequency condition, the slopes of the functions were not clearly different from those for the randomized condition. These results clearly differ from those of Hübner (1996b), which showed, in the spatial two-alternative forced-choice task, steeper psychometric functions for the randomized-frequency condition than those for the fixed- and cued-frequency conditions, supporting the multiple-band model (Hübner, 1993a, 1993b). The difference suggests that the single-band model applies to the uncertainty effects in the temporal forced-choice task, whereas the multiple-band model does so in the spatial forced-choice task.     

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.     

Suprathreshold binocular interactions for grating patterns

Binocular interactions of suprathreshold grating patterns have been investigated using a reaction time measure of contrast detection. Simple reaction times were determined for monocular and binocular viewing conditions over a contrast range from .63 to near threshold. The results from all subjects showed binocular summation for contrast levels near threshold, but there was considerable variation across subjects for contrast levels above threshold. Some subjects showed summation over the entire contrast range, but other subjects showed either binocular inhibition or binocular facilitation for some range of contrast levels. The pattern of binocular interaction for a given subject was consistent for several spatial frequencies. The differences in types of interaction between subjects, the variation in magnitude of binocular interaction with contrast level for each subject, and the data from experiments involving stimulation of noncorresponding retinal areas show that the binocular interactions found for suprathreshold stimuli cannot be accounted for on the basis of probability, and must, therefore, result from physiological interactions between the two eyes. These interactions have been investigated further under conditions of (1) induced fixation disparity, (2) horizontal gratings, and (3) orthogonally oriented gratings.     

The binocular combination of chromatic contrast

How is chromatic contrast combined binocularly? One index of binocularity is the binocular contrast summation ratio (BCSR), which is the improvement in contrast sensitivity with binocular rather than monocular presentation. Simmons and Kingdom (1998, Vision Research 38 1063-1071) noted that BCSRs with some red-green isoluminant stimuli were suggestive of full linear summation. This suggestion was investigated further in four subjects by measuring binocular and monocular contrast thresholds for the detection of 0.5 cycle deg(1) isoluminant (red-green) and isochromatic (yellow-black) Gabor patches. These Gabor patches had either vertically or horizontally oriented carrier gratings and were either dichoptically in phase (same coloured bars in binocular correspondence) or in dichoptic anti-phase (opposite coloured bars in binocular correspondence). Full linear summation would be indicated by BCSRs of 2 for the in-phase and close to 0 for the anti-phase conditions. Mean BCSRs at isoluminance were 1.93 and 0.90, respectively, for the in-phase and anti-phase stimuli with horizontal carriers, the former being consistent with full linear summation, but the latter not. Despite these results, BCSRs obtained with isoluminant and isochromatic stimuli under similar conditions were not statistically distinguishable from each other, although there was a tendency for summation at isoluminance with in-phase stimuli to be higher and anti-phase stimuli to be lower. These data fall short of demonstrating full linear summation of chromatic contrast between the eyes under all presentation conditions, but they do indicate that there are strong binocular interactions at red-green isoluminance, which are similar to, and possibly even stronger than, those obtained with luminance stimuli.     

Binocular interactions in suprathreshold contrast perception

Suprathreshold binocular contrast interactions were studied psychophysically. A split-screen CRT display was used to present separate sine-wave gratings to the observer’s left and right eyes. The method of constant stimuli and a modified method of adjustment were used to find sets of binoculartest patterns that matched a given binocularstandard. Test patterns consisted of the simultaneous presentation of sine-wave gratings that differed in contrast to the left and right eyes. Standard patterns consisted of identical sine-wave gratings presented to the two eyes, and had the same spatial frequency as the test patterns. Binocular contrast matching functions were obtained for several standard contrasts at 1 and 8 c/deg. Binocular matching functions were obtained for luminance increments as well. The binocular contrast matching functions departed from a simple binocular averaging rule, and behaved as if the eye receiving the higher contrast disproportionately dominated the binocular contrast percept. Departures from the binocular averaging rule were slightly greater for higher standard contrasts. Spatial frequency had little effect, and the luminance increment matching functions also departed from the binocular averaging rule. There was evidence for a contrast version of Fechner’s paradox and for substantial individual differences in a form of ocular dominance. In a further experiment, additivity of suprathreshold binocular contrast summation was examined by testing the double-cancellation condition. We found no systematic violations of additivity at 1 and 8 c/deg. Models of suprathreshold binocular contrast summation were examined.     

Contrast and spatial frequency components in visual preferences of newborns

A preferential-looking procedure was used to investigate newborns' responses to square-wave gratings varying in spatial frequency and contrast. A preliminary study confirmed that the gratings used in the experiment were suprathreshold. In the experiment newborns' preference for a grating of 0.1 cycle deg-1 within the peak contrast sensitivity range was examined. Reduction in the contrast of this grating led to a transfer of the preference to a high-contrast grating of the same space-averaged luminance with a spatial frequency outside this range (0.42 cycle deg-1). The findings are discussed with reference to the role of the contrast sensitivity function in pattern preferences of newborns: it is suggested that contrast and spatial frequency interact in determining pattern preferences.     

Weak stimulus generalization using sinusoidal gratings: A cautionary note in animal psychophysics

Psychophysical techniques involving operant and classical conditioning are used commonly to determine the visual thresholds of nonverbal subjects. Typically, subjects are conditioned to respond to a particular stimulus, and once trained sufficiently, the subject’s sensitivity to this and similar stimuli can be determined by decreasing the stimulus intensity until the animal no longer responds. However, this assumes that the animal’s tendency to respond correlates with its sensory abilities. Stimulus generalization to sinusoidal gratings of different spatial frequencies was examined in goldfish. Subjects were classically conditioned to suppress respiration upon presentation of a sinusoidal grating. Animals’ learning curves to each spatial frequency grating were compared in order to determine whether the animals generalized across stimuli. Results indicate that fish show weak stimulus generalization across spatial frequencies. Also, the shape of the contrast sensitivity function, a common measure of the animal’s visual capabilities, is distorted by insufficient training. We conclude that when the goal is to obtain accurate data on visual capabilities, either subjects should be trained to each stimulus to be tested or their generalization gradients should be measured.     

The precision of velocity discrimination across spatial frequency

The precision of velocity coding for moving stimuli of different spatial frequencies was assessed by measuring velocity discrimination thresholds for a 1-c/deg grating paired with a grating whose spatial frequency ranged from 0.25 to 4 c/deg and for grating pairs of the same spatial frequency (0.25, 1, and 4 c/deg). The gratings always moved upward, with velocities ranging from 0.5 to 16 deg/sec, Velocity discrimination was as precise for stimuli that varied in spatial frequency by: ±2 octaves (0.25 vs. 1 c/deg and 4 vs. 1 c/deg) as for stimuli of the same spatial frequency, for specific ranges of velocity that depended on the spatial and, therefore, the temporal frequencies of the stimuli. Compared with a 1-c/deg grating, the perceived velocity of 4-c/deg gratings was about 1.3 times faster and that of 0.25-c/deg gratings was about 1.3 times slower. Although these perceived velocity biases imply variation of velocity-signal processing among spatial frequency channels, the discrimination results indicate that the motion-sensing system can compare signals across different spatial frequency channels to make fine velocity discrimination within appropriate temporal frequency limits.     

Contrast and frequency competition for orientation-contingent color aftereffects

A “competition” paradigm was developed to examine separately the effects of pattern contrast and spatial frequency characteristics on the strength of orientation-contingent color aftereffects (McCollough effects). After adapting to alternately presented red/black and green/black square-wave gratings (one horizontal, one vertical), 11 subjects viewed seven different kinds of test patterns. Unlike Standard McCollough effect test stimuli, the present patterns had variable luminance profiles running both horizontally and vertically within each test pattern area. Forced choice responses were used to determine which aftereffect color (red or green) appeared, as characteristics of vertical and horizontal luminance profiles were varied separately among test stimulus types. We conclude that pattern contrast and human contrast sensitivity account for aftereffect colors in such stimuli. When contrast is taken into consideration, aftereffects are not predicted by similarity between adaptation and test pattern Fourier characteristics, nor are they predicted by the width, per se, of pattern elements.     

Measuring and predicting the effects of alcohol consumption on contrast sensitivity for stationary and moving gratings

Contrast sensitivity was measured for 12 healthy young males while sober, after ingestion of an alcohol placebo, and after ingestion of alcohol (95% grain alcohol; mean estimated blood alcohol level = .088%). Observations were made for both stationary gratings and gratings that traveled through a circular path and required pursuit eye movements. The significant alcohol-related reduction in contrast sensitivity was 2.6 times greater for moving (.29-log-unit reduction) than for stationary gratings (.11-log-unit reduction). The loss in contrast sensitivity for the moving gratings of high spatial frequency (12 cpd) was particularly severe (.37 log unit). Estimated blood alcohol level was correlated with the loss in contrast sensitivity for moving gratings (r = .61), but not with the loss for stationary gratings. Estimated blood alcohol level was strongly correlated with the difference between the loss in contrast sensitivity to moving and stationary gratings (r = .75). These results are consistent with reports that alcohol consumption degrades the ability to make pursuit eye movements. Subjects’ perceived intoxication level was not a reliable predictor of any index of visual performance.     

Spatial disinhibition of orientation analyzers

Following the successive presentation of two masking gratings (M1 and M2), subjects were required to detect the presence or absence of a single vertical line (TS). When the orientations of the two masks were optimal, M1 was able to reduce the masking effect of M2 on the TS. For a vertical TS, disinhibition was maximal when the orientations of M1 and M2 were similar and was minimal when the orientational difference was greater than 15 deg. It is suggested that the spatial selectivity of the disinhibition function reflects the activity of neurons tuned to orientation, and that the disinhibition masking paradigm may be a useful psychophysical technique to measure tuning functions of other feature detectors.     

Purely chromatic perception of motion in depth: two eyes as sensitive as one

Motion hyperacuity (phase) thresholds were measured for both lateral and stereoscopic oscillatory motion in both luminance and equiluminant red/green gratings of 2 cycles per degree. Thresholds for lateral chromatic motion did not exhibit the inhibitory fall-off at low temporal frequencies that was found for luminance motion. Phase thresholds for purely chromatic motion were substantially higher than those for luminance gratings, in proportion to the ratio of cone signal modulation, but they could be predicted from the corresponding contrast sensitivities for both types of stimulus. Stereomovement thresholds in luminance gratings showed the stereomovement suppression effect relative to monocular motion sensitivity previously reported for line stimuli, but purely chromatic gratings did not. Together with the lack of an inhibitory fall-off, these results imply that chromatic and luminance motion are processed by different neural pathways, and that the chrominance pathway is capable of supporting a strong percept of stereoscopic motion from purely chromatic gratings.     

Spatial frequency and the detection of temporal discontinuity in superimposed and adjacent gratings

The properties of the detecting mechanism involved in the resolution of temporal discontinuities of visually presented stimuli have been investigated in two experiments. In Experiment 1, observers made judgments of discontinuity when superimposed presentations of sine-wave gratings of 1, 3, 6, and 10 cycles/deg were presented for either a 20- or a 200-msec duration per presentation at a contrast of .1 and .4. Threshold separation for discontinuity detection indicated a linear increase as spatial frequency increased, with a lesser effect for longer duration exposure and higher contrast. Experiment 2 involved adjacent presentation of the second grating, and a small linear decrease in separation threshold as a function of increasing spatial frequency occurred. The effect of spatial frequency on temporal discontinuity detection is dependent on whether the second stimulus is superimposed or adjacent.     

Figure and ground in space and time: 1. Temporal response surfaces of perceptual organization

The figure-ground organization of an ambiguous bipartite pattern can be manipulated by altering the temporal-frequency content of the two regions of the pattern. Ambiguous patterns in which the two regions of each pattern contained sine-wave gratings of either 8, 4, 1, or 0.5 cycles deg-1 undergoing contrast reversal at rates of 0, 3.75, 7.5, or 15 Hz were tested for figure-ground organization under conditions of equated space-averaged and time-averaged luminance and perceived contrast. All combinations of temporal-frequency differences between the two regions were tested at each spatial frequency. The data are reported for two levels of temporal resolution (15 and 30 s). The pattern region with the relatively higher temporal frequency tended to be seen as the background a higher percentage of the viewing time. There were significant linear trends for the appearance as background of the region of higher temporal frequency with respect to the magnitude of the temporal-frequency difference between the two regions of each pattern for all spatial frequencies and data intervals except the final 15 s interval of the lowest (0.5 cycle deg-1) spatial-frequency condition.     

Laterality differences in sensitivity to line orientation as a function of adaptation duration

Since available evidence indicates that the two cerebral hemispheres are differentially sensitive to different types of stimulus information, and that they also utilize different strategies in processing information, is it possible that the two hemispheres are differentially sensitive to adaptation? Three groups of four subjects each were adapted to black and white gratings using three adapting durations: 500, 1,000, and 5,000 msec. Immediately following adaptation, a test grating was presented in either the left or right visual field. The task of the subject was to determine whether the lines of the adapting and test gratings had the same orientation or not. Analysis showed that in the 5,000-msec and 1,000-msec conditions, more errors occurred with left visual field presentations, responses to left visual field presentations took longer, and a bias-free measure showed that subjects were more sensitive to right visual field presentations. For the 500-msec group, there were no apparent differences between left and right visual fields presentations. The results indicate differential effects of adaptation on the two hemispheres, suggesting sensitivity differences between the two halves of the brain.