Uncertainty impairs grating detection performance in the cat

Using behavioral techniques, contrast thresholds for detection of grating patterns by the cat were measured under conditions of certainty and uncertainty. For certainty trials, the same combination of spatial and temporal frequencies was presented throughout a test session, whereas with uncertainty, the cat was unable to anticipate which of two spatial (or temporal) frequencies would be presented on a given trial. For most spatiotemporal combinations, uncertainty served to elevate contrast thresholds by almost .3 log units, a finding that parallels the outcome found in human vision. The uncertainty paradigm may provide a useful inferential tool for determining channel bandwidth in cat vision.     

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.     

Sensitivity to shearing and compressive motion in random dots

The sensitivity of the visual system to motion of differentially moving random dots was measured. Two kinds of one-dimensional motion were compared: standing-wave patterns where dot movement amplitude varied as a sinusoidal function of position along the axis of dot movement (longitudinal or compressional waves) and patterns of motion where dot movement amplitude varied as a sinusoidal function orthogonal to the axis of motion (transverse or shearing waves). Spatial frequency, temporal frequency, and orientation of the motion were varied. The major finding was a much larger threshold rise for shear than for compression when motion spatial frequency increased beyond 1 cycle deg-1. Control experiments ruled out the extraneous cues of local luminance or local dot density. No conspicuous low spatial-frequency rise in thresholds for any type of differential motion was seen at the lowest spatial frequencies tested, and no difference was seen between horizontal and vertical motion. The results suggest that at the motion threshold spatial integration is greatest in a direction orthogonal to the direction of motion, a view consistent with elongated receptive fields most sensitive to motion orthogonal to their major axis.     

Visual space-time interactions: effects of adapting to spatial frequencies on temporal sensitivity

To study how adaptation to spatial frequency patterns affects temporal sensitivity in vision, observers were selectively adapted for 4 min to either a high- or a low-spatial-frequency sinusoidal grating (12 and 2 cpd, respectively). Their sensitivities to modulation of a blurred patch at high or low temporal frequencies (12 Hz and 2 Hz, respectively) were measured, before and after the adaptation period, by using the yes/no task of signal detection theory. The data consistently indicated that spatial adaptation differentially affected the observers' sensitivities to temporal signals. Specifically, when the observers were adapted to low spatial frequencies, their sensitivity to low temporal frequencies was reduced; when they were adapted to high spatial frequencies, their sensitivity to high temporal frequencies was increased. These results have implications for the psychophysical measurements of temporal and spatial sensitivity, as well as for the issue of the separability of spatial and temporal properties of individual channels.     

Haptic detection of sine-wave gratings

We studied human haptic perception of sine-wave gratings. In the first experiment we measured the dependence of amplitude detection thresholds on the number of cycles and on the wavelength of the gratings. In haptic perception of sine-wave gratings, the results are in agreement with neural summation. The rate at which detection thresholds decrease with increasing number of cycles is much higher than can be accounted for by probability summation alone. Further, neural summation mechanisms describe the detection thresholds accurately over the whole spatial range probed in the experiment, that is wavelengths from 14 mm up to 225 mm. Earlier, we found a power-law dependence of thresholds on the spatial width of Gaussian profiles (Louw et al, 2000 Experimental Brain Research 132 369-374). The current results extend these findings; the power-law dependence holds not only for Gaussian profiles, but also for a broad range of sine-wave gratings with the number of cycles varying between 1 and 8. Haptic perception involves tactual scanning combined with an active, dynamic exploration of the environment. We measured characteristics of the velocity and force with which stimuli were scanned while performing a psychophysical task. One particularly surprising finding was that, without being instructed, participants maintained an almost constant scanning velocity during each 45-min session. A constant velocity in successive trials of the experiment might facilitate or even be necessary for discrimination. Further, a large systematic dependence of velocity on scanning length was found. An eightfold increase in scanning length resulted in about a fourfold increase in scanning velocity. A second experiment was conducted to study the influence of scanning velocity on psychophysical detection thresholds. This was done by systematically imposing specific scanning velocities to the participants while the thresholds were measured. The main result of the second experiment was that psychophysical detection thresholds are constant over a relatively broad range of scanning velocities.     

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.     

Is there low frequency vibrotactile temporal summation?

Reaction times of subjects to threshold vibratory stimuli of various durations and frequencies were measured simultaneously with the thresholds in order to test whether more time is needed for the detection of stimuli of long than short duration at threshold intensities. Vibratory stimuli of 20 or 150 Hz frequency and 50, 150, or 300 ms duration were applied to the back of the hand. Lower detection thresholds and longer reaction times were obtained for both 20 and 150 Hz vibration with increase of stimulus duration. The results suggest that temporal summation of high frequencies is due to energy integration , whereas at low frequencies probability summation explains better the threshold decrement.     

Visual orientation by motion-produced blur patterns: Detection of divergence

Blur patterns are physiological “streaks” of photochemical and neural activity that occur whenever an observer and his visual environment are in relative motion. When retinal velocities are high, the impression of visual “flow” gives way to one of a field of “blur lines” whose patterns are rich with information about the motions and the optical textures that produced them. Simulated blur patterns were produced and thresholds measured for the detection of divergence at nine retinal loci. Sensitivity was somewhat greater in the central retina. Thresh-olds remained the same despite variations in pattern velocity, number of elements, and the presence or absence of an internal velocity gradient. Observers were able to orient above-threshold patterns, but consistently underestimated the amount of slant.     

Integration of speed signals in the direction of motion

Speed discrimination tasks were used to examine the spatial and temporal characteristics of the integration mechanism involved when signals are extended in the direction of motion. We varied the aspect ratio of a signal patch whose speed differed from the background, while holding the area of the signal patch constant, so that the signal patch could be either extended in the direction of motion or extended orthogonal to the direction of motion. Speed discrimination thresholds decreased dramatically as the signal patch was extended in the direction of motion. The spatial and temporal integration regions were larger than would be expected if the integration mechanism were a low-level motion detector. The mechanism was tuned for direction of motion. The data are discussed with reference to two alternative integration mechanisms: a low-level detector that is elongated in the direction of motion and a higher level integration mechanism characterized by cooperative or facilitatory interactions between low-level detectors tuned to the same direction of motion. Our data are consistent with a second-level, direction-specific process that integrates the responses of low-level motion 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.     

Extent-of-motion thresholds under subject-relative and object-relative conditions

The experiment was designed to discover the threshold extent of motion at medium speeds amounting to 41, 82, and 164 min./sec., and to compare the perception of motion arising from subject-relative displacement with the perception of motion arising from object-relative displacement. Extent thresholds were found while velocity was kept constant. Different groups of ten Ss were used for each displacement velocity, and for each S the extent threshold was twice obtained by the method of constant stimuli, once under subjectrelative and once under object-relative displacement conditions. Sensitivity to brief displacements of a continuously visible target was high; average thresholds ranged from 1.0 to 4.4 min. under the various conditions employed. The thresholds were higher for subject-relative conditions and the slower displacement velocities and lower for objectrelative conditions and faster displacements.     

Extent-of-motion thresholds under subject-relative and object-relative conditions

The experiment was designed to discover the threshold extent of motion at medium speeds amounting to 41, 82, and 164 min./sec., and to compare the perception of motion arising from subject-relative displacement with the perception of motion arising from object-relative displacement. Extent thresholds were found while velocity was kept constant. Different groups of ten Ss were used for each displacement velocity, and for each S the extent threshold was twice obtained by the method of constant stimuli, once under subjectrelative and once under object-relative displacement conditions. Sensitivity to brief displacements of a continuously visible target was high; average thresholds ranged from 1.0 to 4.4 min. under the various conditions employed. The thresholds were higher for subject-relative conditions and the slower displacement velocities and lower for objectrelative conditions and faster displacements.     

An oblique effect of chromatic gratings measured by color-mixture thresholds

Contrast sensitivity is lower for obliquely oriented achromatic gratings than for vertical or horizontal gratings at high spatial and low temporal frequencies. Although this response is suggestive of mediation by P-pathway cortical correlates, no clear sensory (i.e. class 1) oblique effect has been demonstrated with isoluminant chromatic stimuli. In the present experiment, a two-alternative forced-choice detection task was used to measure observers' sensitivity to spatiotemporal sinusoids varying in orientation and color contrast. A maximum-likelihood method fit ellipses to the thresholds, with the length of each ellipse taken as a measure of chromatic contrast sensitivity at isoluminance, and the width as luminance contrast threshold. A chromatic oblique effect was observed at about 3 cycles deg-1 suggesting an orientation bias within the cortical stream conveying P-cell activity.     

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.     

Velocity not acceleration of self-motion mediates vestibular-visual interaction

We investigated the influence of vestibular stimulation with different angular accelerations and velocities on the perception of visual motion direction. Constant accelerations resulting in different angular velocities and constant angular velocities obtained at different accelerations were combined in twenty healthy subjects. Random-dot kinematograms with coherently moving pixels and randomly moving pixels were used as visual stimuli during whole-body rotations. The smallest percentage of coherently moving pixels leading to a clear perception of motion direction was taken as the perception threshold. Perception thresholds significantly increased with increasing angular velocity. Increased acceleration, however, had no significant effect on the perception thresholds. We conclude that the achieved angular velocity, and not acceleration, is the predominant factor in the processing of vestibular-visual interaction.     

Temporal integration and contrast sensitivity in foveal and peripheral vision

Spatial contrast sensitivity functions and temporal integration functions for gratings with dark surrounds were measured at various eccentricities in photopic vision. Contrast sensitivity decreased with increasing eccentricity at all exposure durations and spatial frequencies tested. The decrease was faster at high than at low spatial frequencies, but similar at different exposure durations. When cortically similar stimulus conditions were produced at different eccentricities by M-scaling, contrast sensitivity became independent of visual field location at all exposure durations tested. The results support the view that in photopic vision spatiotemporal information processing is qualitatively similar across the visual field, and that quantitative differences result from retino-topical differences in ganglion cell sampling. For gratings of constant retinal area temporal integration (improvement of contrast sensitivity with increasing exposure duration) was more extensive at high than at low retinal spatial frequencies but independent of cortical spatial frequency and eccentricity. For M-scaled gratings temporal integration was more extensive at high than at low cortical spatial frequencies but independent of retinal spatial frequency and eccentricity. The results suggest that the primary determinant of temporal integration is not spatial frequency but grating value that is calculated as AF2 square cycles (cycle2), where A is grating area and F spatial frequency.     

Visual acceleration detection: effect of sign and motion orientation

Thresholds for the detection of constant acceleration and deceleration of a discrete object moving along horizontal and vertical axes were studied. A staircase methodology was used to determine thresholds for three average velocities (0.7, 1.2, and 1.7 deg/sec). Thresholds, expressed as the proportion of velocity change, did not differ significantly among the average velocities; thus, a consistent Weber-like fraction is suggested by the data. Furthermore, there was an interaction between the axis of motion (horizontal or vertical) and the sign of the velocity change (acceleration or deceleration): accelerations were easier to detect along the vertical axis, decelerations along the horizontal axis.     

Perfect visual short-term memory for periodic patterns

Abstract

The short-term memory for spatial frequency information was assessed by measuring the spatial frequency discrimination thresholds for briefly flashed luminance gratings as a function of the time interval between the test and reference gratings, using a computer-controlled two-interval forced-choice procedure. Discrimination thresholds were stable for interstimulus intervals in the range 1–30 sec under all conditions tested. At low contrasts, short exposure times and low spatial frequencies discrimination thresholds increased, but no interactions between stimulus parameters affecting thresholds and interstimulus interval were observed. It is concluded that factors limiting spatial discrimination are associated with the sensory coding stage. Spatial discrimination and visual memory may be based on a common representation, which is perfectly retained in short-term memory. Visual half-field tests revealed no hemispheric differences in the processing and retention of spatial frequency information.     

The effect of temporal and spatial frequency on phantom-contour detection

Phantom contours are a visual illusion that can define regions with distinctive boundaries when no real surrounding edges exist. Spatial-frequency sensitivity is known to vary reliably across the visual-processing pathways, as does temporal-frequency sensitivity. Given that the effect of temporal frequency on phantom-contour detection has been previously established, and that the relationship between spatial frequency and temporal frequency is known, two experiments were designed to measure the highest level of spatial frequency that would still allow reliable pattern detection at different temporal frequencies by using the phantom-contour paradigm. The results revealed that phantom-contour detection is impaired when the stimulus has a high spatial-frequency content and that phantom-contour perception is supported by low spatial frequencies.     

Movement detection thresholds and stimulus duration

Movement detection thresholds were measured for varying exposures of a moving spot. A tradeoff was found in which an increase in duration (T) was offset by a decrease in the velocity required for detection (V). In the range of durations studied (about 50–700 msec), V × T was constant. The V × T constancy was interpreted in terms of the direct detection of movement as motion, and a comparison was made with Bloch’s law.