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PubMed1988

Shape similarity and distance disparity as apparent motion correspondence cues.

Apparent motion is perceived when two spots of light are presented successively in different locations. When more than one element is present in each frame, there is a correspondence problem in matching the elements in one frame with those in the other. We report the effects of shape similarity and distance disparity on the correspondence process. Twenty subjects were tested using a 2-AFC design. We found that both shape and distance cues are used by the correspondence process: when distance is the only cue the motion which is usually perceived is that involving the shorter distance; when shape is the only cue the motion involving two elements of the same shape is preferred. We also studied the interaction between the two cues when both were present. Quantitative measures of the relative strengths of these effects and of their interaction are reported. A Signal Detection Theory model is used to analyze these apparent motion correspondence effects.

Cues↗
PubMed1988

Changing size (looming) as a stimulus to accommodation and vergence.

Changing size (looming) produces changes in accommodation and vergence. Dynamic responses of vergence and accommodation to sinusoidal looming of a Maltese cross were recorded with an SRI dual-Purkinje-image eyetracker and optometer. The ratio of these two motor responses was compared with the response accommodative convergence/accommodation (AC/A) ratio and convergence accommodation/convergence (CA/A) ratio determined from sinusoidal variations of blur and disparity respectively. The response to changing size was found to be more similar to the AC/A ratio than the CA/C ratio. In addition, when a changing disparity or changing blur stimulus was combined with a changing size stimulus, the response phase lags of accommodation and vergence were decreased. In addition, the CA/C ratio was increased when changing size was added to changing disparity, but the AC/A ratio was unaltered when changing size was added to changing blur. These results indicate that changing size is stimulating accommodation directly and vergence secondarily through an AC/A crosslink.

Accommodation, Ocular↗
PubMed1989

The conditions under which Mach bands are visible.

In this paper we challenge the classical explanation of Mach bands--that they result from lateral inhibitory mechanism operating in the visual system--and present an alternative explanation based on a recent local energy model of feature detection (Morrone & Burr, 1988). A series of experiments was conducted to establish the range of parameters under which Mach bands appear on periodic waveforms of the trapezoid family. The model predicts successfully the conditions under which Mach bands appear, and the contrast necessary to see them. Other models, including those based on lateral inhibition and band-pass filtering fail to do so.

Contrast Sensitivity↗
PubMed1990

Spatial-filter selection in large-scale spatial-interval discrimination.

Spatial-interval discrimination thresholds were measured for a pair of bars in the presence of other parallel bars placed far enough from the targets as to be outside the range of neural and optical blurring. Thresholds were elevated when the targets were embedded in an array of four parallel bars (two between and two flanking the targets), but not when there were only two parallels, whether the parallels were between the target bars or flanking them. The threshold elevation was larger with a 100-msec than with a 500-msec exposure duration. Attenuating the high spatial frequencies magnified the threshold elevation. The data indicate that the process responsible for spatial-interval discrimination automatically selects which spatial filters to use; it does not have to scan through all ranges of spatial filters.

Contrast Sensitivity↗
PubMed1990

The role of separation and eccentricity in encoding position.

We measured two- and three-line spatial interval and alignment thresholds for a wide range of separations and eccentricities. In order to avoid confounding the role of separation and eccentricity, the test lines were presented on iso-eccentric arcs, with radii between 0.625 and 10 deg. The iso-eccentric paradigm allows separation to be varied over a large range while holding eccentricity constant. Our main finding is that for all tasks, at all eccentricities, Weber's law fails at large separations. Our results are consistent with the hypothesis that distance judgements are limited by at least two factors: (1) when the separation of the iso-eccentric test lines is small with respect to the eccentricity position thresholds are proportional to the separation of the features, and show little dependence on eccentricity. This is Weber's law for position, and the threshold is approx. 0.03-0.05 times the stimulus separation; (2) when the separation of the iso-eccentric test lines is comparable in size to the eccentricity, position thresholds are proportional to the target eccentricity, and are essentially independent of separation. In this "eccentricity regime", position discrimination thresholds are = ECC * k where ECC is the stimulus eccentricity in degrees, and k is a fraction of the eccentricity (approximately 0.01-0.03). The observer uses whichever mechanism is more sensitive to the stimulus. Under the conditions of our experiments, the observers perform a Weber computation when the separation, S, between the pair of iso-eccentric test lines is less than about 0.5 * ECC, and apply a "cortical ruler" when S is greater than about 0.5 * ECC. If the angle subtended by the fixation point and the pair of iso-eccentric test lines is considered, then for both the two-line and the three-line tasks, when the angle is less than approx. 30 deg, thresholds are proportional to separation, and when it is between 30 and 180 deg, thresholds are proportional to eccentricity.

Discrimination, Psychological↗
PubMed1990

The role of image size and retinal motion in the computation of absolute distance by the Mongolian gerbil (Meriones unguiculatus).

In a series of experiments in which Mongolian gerbils were trained to jump over a variable gap, it was demonstrated that computation of the distance to be jumped was dependent on both image size and retinal motion, the latter cue being generated by the production of vertical translation movements of the head (head bobs). When image size was not a reliable cue, the animals produced more head bobs, thereby increasing the availability of retinal motion cues. The performance of the gerbils on various probe trials strongly suggested that they computed absolute distance by combining information about the velocity (or amplitude) of their head bobs with information about the velocity (or displacement) of the moving image of the landing platform.

Animals↗
PubMed1990

Motion segregation from speed differences: evidence for nonlinear processing.

This paper examines observers' ability to detect regions delimited by speed differences. Several types of translational motion stimuli, of varying task difficulty, were tested over a wide range of base speeds. The observer's task was to decide whether a region of dots moving at a different speed from the base speed was located to the left or right of the display's center. Both increments (dots within the test region moving faster than the base speed) and decrements (dots within the test region moving slower than the base speed) were examined. When the task was relatively difficult the following asymmetries were found: at slow base speeds, incremental thresholds were lower than decremental thresholds; at fast base speeds, the reverse pattern occurred. When the task was relatively easy, no consistent asymmetries were found. It is proposed that the visual system encodes speed through a sigmoidal nonlinear response function, and it is shown that this one nonlinearity can be used to explain results for both easy and difficult tasks.

Differential Threshold↗
PubMed1990

Biases and sensitivities in geometrical illusions.

Psychometric functions were collected to measure biases and sensitivities in certain classical illusory configurations, such as the Müller-Lyer. We found that sensitivities (thresholds or just noticeable differences) were generally not affected by the introduction of illusory biases, and the implications of this for theories of the illusions are discussed. Experiments on the Müller-Lyer figure showed that the effect depends upon mis-location of the ends of the figure, rather than upon a global expansion as demanded by the size-constancy theory. A new illusion is described in which the perceived position of a dot is displaced towards the centre of a surrounding cluster of dots, even though it is clearly discriminable from other members of the cluster by their colour. We argue that illusions illustrate powerful constraints upon visual processing: they arise when subjects are instructed to carry out a task to which the visual system is not adapted.

Distance Perception↗
PubMed1992

Accommodative hysteresis as a function of target--dark focus separation.

The concept of dark focus (DF) as fulcrum for accommodative effort was examined by inducing adaptation of tonic accommodation with the target at varying dioptric distances from the DF. Mean pre- to post-changes in DF at the initial post fixation test essentially were linear (r2 = 0.975), with zero intercept, with respect to the target-DF separation, as were the data of most individual subjects. Target-DF distance thus is a major determinant of adaptation of tonic accommodation. These results are consistent with the interpretation of DF as a zero reference point or fulcrum about which accommodative effort varies.

Accommodation, Ocular↗
PubMed1992

Contrast sensitivity as a function of spatial frequency, viewing distance and eccentricity with and without spatial noise.

Using computer graphics and a two-alternative forced-choice method we measured threshold contrast as a function of viewing distance, spatial frequency, and eccentricity for gratings with and without added, white two-dimensional spatial noise. Our experiments showed that in spatial noise contrast sensitivity was independent of viewing distance as long as contrast sensitivity was lower with noise than without. With increasing spatial frequency (f) the grating area (A) was reduced in order to keep the relative grating size (Af2) constant. At all spatial frequencies the test gratings thus had the same amount of detail and contour. Noise spectral density was reduced in direct proportion to grating area in order to keep the physical signal-to-noise ratio constant. An increase in spatial frequency was thus accompanied with reductions in grating area and noise spectral density similar to those produced by a corresponding increase in viewing distance. In agreement, contrast detection in spatial noise was found to be independent of spatial frequency as long as contrast sensitivity was lower with noise than without. The effect of increasing eccentricity on visual performance can be compensated for by reducing the viewing distance (M-scaling). Hence, without M-scaling the effect of increasing eccentricity is similar to that of increasing viewing distance. In agreement, we found that contrast sensitivity in spatial noise was independent of eccentricity as long as contrast sensitivity was lower with noise than without.

Adult↗
PubMed1993

Lateral interactions between spatial channels: suppression and facilitation revealed by lateral masking experiments.

We measured contrast detection thresholds for a foveal Gabor signal flanked by two high contrast Gabor signals. The spatially localized target and masks enabled investigation of space dependent lateral interactions between foveal and neighboring spatial channels. Our data show a suppressive region extending to a radius of two wavelengths, in which the presence of the masking signals have the effect of increasing target threshold. Beyond this range a much larger facilitatory region (up to a distance of ten wavelengths) is indicated, in which contrast thresholds were found to decrease by up to a factor of two. The interactions between the foveal target and the flanking Gabor signals are spatial-frequency and orientation specific in both regions, but less specific in the suppression region.

Contrast Sensitivity↗
PubMed1995

The effect of perceived distance on accommodation under binocular steady-state conditions.

Spatiotopic cues, such as perceived distance, have little effect on accommodation unless blur has been reduced or eliminated. We investigated the effect of perceived distance on accommodation under binocular steady-state conditions, about which little is known. Blur was reduced but not eliminated by using a stimulus with a moderately low luminance. Accommodation was measured under two conditions: (1) when cues from perceived distance, blur, and convergence were aligned; and (2) when perceived distance was opposed by both blur and convergence. We found a significant difference in accommodation between the two conditions, which we attribute to perceived distance.

Accommodation, Ocular↗
PubMed1994

Active vision in honeybees: task-oriented suppression of an innate behaviour.

In a pattern discrimination task, bees tend to fly along the contours contained in the patterns, as revealed by an earlier study. As opposed to this, in a task involving the detection of an edge between two striped surfaces placed at two different ranges, the bees avoid contour-following, as revealed by the present study. The study shows that, in the latter task, the bees learn to suppress the otherwise innate contour-following behaviour and adopt a flight strategy that provides them with the motion parallax cues necessary to cope with this task. Thus, the animal's active behaviour determines the type of visual information to be extracted from the environment.

Animals↗
PubMed1994

Resistance to positional noise scales with target size.

The ability to judge the separation between two target lines deteriorates as the base separation increases. Several lines of evidence suggest that this may be due to larger base separations being processed by mechanisms that cover larger areas and which have a greater associated positional uncertainty as a consequence. Separation discrimination was measured as a function of base separation with randomly jittering targets. As predicted from the above models the resistance to positional noise increased in proportion to base separation of the targets. The data is incompatible with the suggestion that resistance to positional noise declines when the extent of the noise exceeds fixational instability.

Discrimination, Psychological↗
PubMed1995

Rotation of Listing's plane by horizontal, vertical and oblique prism-induced vergence.

We examined the changes in Listing's plane resulting from prismatically induced vergence. The three-dimensional angular positions of the two eyes were compared in normal subjects wearing search coils and gazing at targets 1.9 m away with and without prisms. For horizontal base-out prisms each degree of convergence in one eye yielded 0.72 deg of temporal rotation of Listing's plane in that eye. The results from vertical prisms were not what was expected from the horizontal results. A base-up prism on the right eye induced a downward and temporal rotation of Listing's plane. A base-down prism on the right eye induced an upward and nasal rotation of Listing's plane. The effects of oblique prisms were those expected from combining the effects of horizontal and vertical prisms. Thus in addition to producing a horizontal or vertical misalignment of the gaze line, prisms induce an unexpected position-dependent torsional disparity.

Convergence, Ocular↗
PubMed1995

Unequal amplitude saccades produced by aniseikonic patterns: effects of viewing distance.

This study describes differences in horizontal and vertical disconjugate saccades under far and close viewing conditions of two dichoptically presented aniseikonic random checkerboard patterns. At far viewing, disconjugacy of horizontal saccades requiring divergence was accomplished intrasaccadically after several minutes; for convergence the intrasaccadic disconjugacy was limited. Size differences partially persisted in open-loop trials. At close viewing intrasaccadic divergent changes in conjugacy were instantaneous, but motor storage during open-loop was absent. It is concluded that disconjugate saccades to targets at far distance lead to an adaptation process, whereas at close viewing distance horizontal disparity is a visual compensation process used directly to scale the relative amplitudes of both eyes, not leading to adaptation. The time-course of disconjugate vertical saccades was much slower, with mostly postsaccadic vergence. Nearby viewing enhanced the disconjugacy of vertical saccades.

Adaptation, Physiological↗
PubMed1995

Unequal saccades produced by aniseikonic patterns: a model approach.

This study addresses a possible mechanism for fast disconjugate adaptation of binocular horizontal saccades. Disconjugacy of binocular saccades was elicited by two dichoptically presented, identical but aniseikonic, random checkerboard patterns. Adaptation was achieved with the patterns at far distance (144 cm). In this condition, which requires a relatively small (8%) size difference of the saccades, a short learning period was mandatory for the binocular saccades to become disconjugate. The saccadic modifications were superimposed on an idiosyncratic pattern of intra-saccadic yoking. A model of saccadic signal generation is described, that has been used to separate the contributions on saccadic disconjugacy provided by modification of visual inputs processing, which alters the motor-system inputs, and by modification of the control system: the adaptation. We identified three major components of the saccadic command (two phasic and one tonic) that contribute and in a specific way to the saccadic yoking and disconjugacy. The model analysis proposes that separate control mechanisms exist operating on these phasic and tonic signals. We show that the saccadic system can generate the vergence component shown by our aniseikonic saccades. We discuss a distributed-parallel implementation of the saccadic system able to provide both the conjugate and disconjugate components of control.

Adaptation, Physiological↗
PubMed1996

Psychophysical end-stopping associated with line targets.

Increment threshold for a small (e.g. 1' x 5') line target superimposed on backgrounds of various shapes and sizes was measured to provide a detailed map of the spatial interactions about line targets. This modified "Westheimer paradigm" indicated sensitization in the length direction as well as in the width direction around the line target. The effect of the adaptation field summed over an elongated, end-tapered central region, and showed strong end-zone antagonism beyond the ends of the elongated summation area, as well as flank antagonism to the sides. Secondary disinhibitory and inhibitory areas outside of the antagonistic surround were also demonstrated. When length of the test line was varied, the length of the summation region increased concomitantly, while the length of the end-zones remained fixed. End-zone antagonism was slightly weaker at oblique orientations. These results demonstrate a perceptual analog to neurophysiological end-stopping, and suggest a multilobed y-dimension weighting profile appropriate for models of spatial visual abilities.

Adaptation, Ocular↗