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Form from motion parallax and form from luminance contrast: vernier discrimination.

UNLABELLED: Some objects are perfectly camouflaged when stationary, but are clearly visible when moving; the boundaries of such an object are defined entirely by motion parallax. Little is known about the eye's ability to make spatial discriminations between motion-defined objects. In this study, subjects viewed a pseudo-random pattern of dots within which a camouflaged bar was made visible by relative motion of dots. Vernier acuity for the motion-defined bar was 27-45 sec arc for three subjects, much less than the interdot separation of 360 sec arc, much less than the 2 deg receptive field size for motion, and comparable with the foveal intercone separation of 30 sec arc. It is proposed that an opponent-orientation process and an opponent-position process can both contribute to vernier judgements for motion-defined objects. Real-world motion contrast commonly confounds the following cues for figure-ground segregation: (1) different texture velocities on either side of the figure's boundary; (2) in any given time interval, texture in figure and ground moves different distances; and (3) texture continually appears and disappears along the figure's boundary. When cues (2) and (3) were eliminated, thus ensuring figure-ground segregation was achieved entirely by motion-sensitive neural elements, vernier acuity was 44 +/- 5 sec arc compared with 36 +/- 8 sec arc for a dotted bar defined by luminance contrast. CONCLUSION: Vernier acuity for a dotted bar whose boundary was defined entirely by motion-sensitive neural elements was similar to vernier acuity for a dotted bar whose boundary was defined by luminance contrast.

Contrast Sensitivity↗

Stereo and motion parallax cues in human 3D vision: can they vanish without a trace?

In an immersive virtual reality environment, subjects fail to notice when a scene expands or contracts around them, despite correct and consistent information from binocular stereopsis and motion parallax, resulting in gross failures of size constancy (A. Glennerster, L. Tcheang, S. J. Gilson, A. W. Fitzgibbon, & A. J. Parker, 2006). We determined whether the integration of stereopsis/motion parallax cues with texture-based cues could be modified through feedback. Subjects compared the size of two objects, each visible when the room was of a different size. As the subject walked, the room expanded or contracted, although subjects failed to notice any change. Subjects were given feedback about the accuracy of their size judgments, where the "correct" size setting was defined either by texture-based cues or (in a separate experiment) by stereo/motion parallax cues. Because of feedback, observers were able to adjust responses such that fewer errors were made. For texture-based feedback, the pattern of responses was consistent with observers weighting texture cues more heavily. However, for stereo/motion parallax feedback, performance in many conditions became worse such that, paradoxically, biases moved away from the point reinforced by the feedback. This can be explained by assuming that subjects remap the relationship between stereo/motion parallax cues and perceived size or that they develop strategies to change their criterion for a size match on different trials. In either case, subjects appear not to have direct access to stereo/motion parallax cues.

Adult↗

Unraveling adaptation and mutual inhibition in perceptual rivalry.

When the visual system is confronted with incompatible images in the same part of the visual field, the conscious percept switches back and forth between the rivaling stimuli. Such spontaneous flips provide important clues to the neuronal basis for visual awareness. The general idea is that two representations compete for dominance in a process of mutual inhibition, in which adaptation shifts the balance to and fro. The inherent nonlinear nature of the rivalrous flip-flop and its stochastic behavior, however, made it impossible to disentangle inhibition and adaptation. Here we report a general method to measure the time course, and asymmetries, of mechanisms involved in perceptual rivalry. Supported by model simulations, we show the dynamics of opponent interactions between mutual inhibition and adaptation. The findings not only provide new insight into the mechanism underlying rivalry but also offer new opportunities to study and compare a wide range of bistable processes in the brain and their relation to visual awareness.

Adaptation, Physiological↗

Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations.

PURPOSE: The present study was designed to elucidate the molecular genetic basis of a congenital stationary cone dysfunction characterized by congenital nystagmus, moderate visual impairment, and markedly disparate color vision deficiencies between two affected cousins. METHODS: Ophthalmic examinations with emphasis on color vision and electrophysiology. Molecular genetic analysis of the X-linked cone opsin genes, mutation screening of the CNGA3, CNGB3, and GNAT2 genes, and heterologous splicing experiments. RESULTS: Whereas the proband was found to carry a homozygous frameshift mutation (Tyr95fs) in GNAT2, her cousin was compound heterozygous for the Tyr95fs and a new intronic mutation c.461 + 24G-->A. Heterologous expression in COS7 cells showed that the latter causes a splicing defect that results in early translation termination. Yet, this mutation is leaky, giving rise to small amounts of correctly spliced transcripts and offer an explanation for the diverging clinical findings in the cousins, one best described as incomplete achromatopsia and the other with oligocone trichromacy. CONCLUSIONS: The cases presented broaden the phenotypic spectrum of GNAT2 mutations and underline the increasing importance of molecular genetics in the clinical diagnosis of atypical ophthalmic phenotypes.

Adolescent↗

Reduced occipital regional volumes at term predict impaired visual function in early childhood in very low birth weight infants.

PURPOSE: Premature infants are at increased risk of impaired visual performance related to both cortical and subcortical pathways for oculomotor control. The hypothesis for the current study was that preterm infants with impaired saccades, smooth pursuit, and binocular eye alignment at age 2 years would have smaller occipital brain volumes at term equivalent, as measured by volumetric magnetic resonance (MR) techniques, than would preterm infants without such abnormalities. METHODS: Study participants consisted of 68 infants from a representative regional cohort of 100 preterm infants born between 23 and 33 weeks' gestation. At term equivalent, all infants underwent MR imaging, and the images were coregistered, tissue segmented into five cerebral tissue subtypes, and further subdivided into eight regions for each hemisphere. At 2 years corrected, all infants completed a comprehensive orthoptic evaluation performed by a single examiner. RESULTS: Twenty-four (35%) of the 68 infants had abnormal oculomotor control at 2 years, including abnormalities in saccadic movements (n = 7), smooth pursuit (n = 14), or strabismus (n = 9, four with esotropia and five with exotropia). When compared with preterm infants without visuomotor impairment, these infants had significantly smaller inferior occipital region brain tissue volumes bilaterally (n = 24 vs. n = 44; total tissue, mean +/- SD, left, 37.9 +/- 7.4 cm(3) vs. 43.7 +/- 7.4 cm(3); mean difference [95% CI] -5.7 [-9.4 to -2.0] cm(3), P = 0.003; right, 36.8 +/- 7.1 cm(3) vs. 41.4 +/- 6.2 cm(3), mean difference -4.6 [-7.9 to -1.3] cm(3), P = 0.007). This difference remained significant after adjusting for intracranial volume (ICV; left, mean difference -3.5 [-6.7 to -0.2] cm(3), P = 0.04; right, mean difference -2.4 [-5.2 to -0.4] cm(3), P = 0.09). Within this region, the cortical gray matter volume was the most significantly reduced (left, 20.4 +/- 6.2 cm(3) vs. 25.4 +/- 5.6 cm(3), mean difference -3.1 [-5.7 to -0.5] cm(3), P = 0.02; right 21.0 +/- 5.4 cm(3) vs. 24.9 +/- 5.0 cm(3), mean difference -2.2 [-4.4 to 0.0] cm(3), P = 0.05, ICV adjusted). Abnormalities in saccadic eye movements accounted for the largest effect on inferior occipital regional brain volumes (left side, P = 0.02). CONCLUSIONS: Volumetric MR imaging techniques demonstrated an overall reduction in the inferior occipital regional brain volumes in preterm infants at term corrected who later exhibit impaired oculomotor function control. These findings assist in understanding the neuroanatomic correlates of later visual difficulties experienced by infants born prematurely.

Child, Preschool↗

Using stereokinetic effect to convey depth: computationally efficient depth-from-motion displays.

Recent developments in microelectronics have encouraged the use of 3D data bases to create compelling volumetric renderings of graphical objects. However, even with the computational capabilities of current-generation graphical systems, real-time displays of such objects are difficult, particularly when dynamic spatial transformations are involved. In this paper we discuss a type of visual stimulus (the stereokinetic effect display) that is computationally far less complex than a true three-dimensional transformation but yields an equally compelling depth impression, often perceptually indiscriminable from the true spatial transformation. Several possible applications for this technique are discussed (e.g., animating contour maps and air traffic control displays so as to evoke accurate depth percepts).

Aircraft↗

Modified astigmatism dial diagram for locating eccentric fixation in patients with central scotoma.

PURPOSE: Patients with central scotoma often develop eccentric fixation on a preferred retinal locus (PRL). Identifying the PRL is one of the first steps in low vision rehabilitation training. We present our evaluation of a simple test designed to locate the eccentric fixation in eyes with central scotoma. METHODS: This was a prospective case series of consecutive patients with age-related macular degeneration and bilateral central scotoma. A numeral was added in the center of an astigmatism dial diagram. After one eye was patched, patients with central scotoma were asked to fixate the dial and describe it, then to look at the 12 o'clock position, and then around the clock. The eccentricity at which the central numeral was best seen was compared with the one determined by scanning laser ophthalmoscopy (SLO). The modified astigmatism dial test and SLO were done independently by two masked investigators. The results of the two methods were expressed in clock hour positions and were considered to be in agreement when they did not differ by more than one hour. RESULTS: Nine consecutive patients (18 eyes) with severe age-related macular degeneration and bilateral central scotoma were tested. The six women and three men ranged in age from 61 to 86 years (mean 75.8 years). The pattern test correlated with SLO findings in 12 (66%) of the 18 eyes. When considering the best-seeing eye of each patient, results showed agreement in eight (88%) out of nine cases. CONCLUSIONS: The modified astigmatism dial test appears useful for establishing the location of the eccentric fixation in the best-seeing eye of patients with bilateral central scotoma, allowing visual rehabilitation training to be started without delay.

Aged↗

A statistical model for binocular rivalry.

A probabilistic model is presented for the phase durations in binocular rivalry experiments. The hypothetical construct of inhibition or reaction inhibition is used to account for the length of the successive phases of left-eye dominance and right-eye dominance. In accordance with Hull's Postulate X.B. it is assumed that the inhibition increases linearly at rate a1 during periods of left-eye dominance and decreases linearly at rate a0 during periods of right-eye dominance. Two different versions of the proposed model are presented: the beta and the Bessel inhibition models. Inhibition fluctuates between the boundaries 0 and 1 in the beta inhibition model and between -infinity and +infinity in the Bessel inhibition model. The transition rates lambda1(t) for switches from a state of left-eye dominance to a state of right-eye dominance, and lambda0(t) for switches from a state of right-eye dominance to a state of left-eye dominance depend on inhibition: lambda1(t)=l1 (Y(t)), lambda0(t)=l0(Y(t)), where l1 is a non-decreasing function and l0 is a non-increasing function. In the beta inhibition model l1(y)=c1/(1 - y) and l0(y)=c0/y. In the Bessel inhibition model l1(y)=u1e(y) and l0(y)=u0/e(y). Special attention is given to the derivation of the expectation of the stationary phase durations.

Functional Laterality↗

Efficiency of stereopsis in random-dot stereograms.

The statistical efficiency of stereopsis was investigated by measurement of the discriminability d' of a step edge in depth in a random-dot stereogram and its comparison with d' calculated for an ideal observer model. Efficiencies of approximately 20% were found for stimuli with very few (less than 30) dots. As the number of dots was increased, efficiency fell markedly to 2% and below. Over the ranges explored in this study, there was little variation in efficiency with changes in dot density (with dot number constant) or stimulus size. Efficiency loss was also found to be almost entirely due to incomplete use of the available information rather than to intrinsic observer variance. Results were compared with two simple models that implemented possible detection strategies.

Depth Perception↗

Method for representing quantitatively whole properties of visual patterns.

It was assumed that there is a variable, named "strength of fusion," underlying binocular fusion and rivalry. The strength of fusion is the resistance of the fused left- and right-eye patterns to separation. The first task was to obtain a measure of the strength of fusion and the second to examine the strength of fusion as a function of various differences of the patterns. The experiments showed that the angular separation only in the temporalward direction could be used as an appropriate measure of the strength of fusion and its value was maximum when the patterns were identical and decreased as the difference increased. This result supports the assumption about the strength of fusion.

Adult↗

Spatial discrimination in children with poor vergence control.

In a 1987 study of children with reading difficulties, Stein, Riddell, and Fowler observed a relationship between poor vergence control, as indicated on a synoptophore vergence test, and the children's problems with learning to read. They suggested that poor vergence control led to impaired accuracy of spatial localisation and that this impeded learning to read. Here we have compared the accuracy of spatial localisation on a nonlinguistic computer game by children having good and poor vergence control. The children with poor vergence control made significantly more errors when locating targets than children with good vergence control. These results lend further support to the hypothesis that some children do not learn to read because they are unable to determine accurately the positions of letters in words.

Attention↗

How does the visual system distinguish between illuminance and reflectance?

The experiments in which the strengths of pattern and of fusion differing in kind from brightness were used as measures indicated that the visual system could distinguish between illuminance and reflectance. From this result and an observation of gray papers by a microscope, it is assumed that luminance has two aspects, one refers to the macroscopic density of photons and another to the proportion of the reflected microscopic areas to the absorbed microscopic areas so that brightness constancy occurs in relation to each of the patterns of the various sizes from a macroscopic pattern visible to the naked eye to a microscopic pattern not visible. It is also mentioned that the strength of fusion is rare but promising as a measure for analyzing brightness.

Attention↗

Theoretical parallels between the Ponzo illusion and the Wundt-Jastrow illusion.

Misapplied-size-constancy, assimilation, and contrast theories are discussed as explanations for the Wundt-Jastrow and Ponzo illusions. An experiment is reported that questions the need to include a contrast function in the assimilation theory of Pressey and Wilson to account for the Wundt-Jastrow illusion. Several directions for further research are proposed.

Adult↗

Motion parallax, relative size, and Benussi effect.

Many observers perceive depth when a configuration of nonconcentric circles is rotated on a disc. While it has been suggested by a number of investigators that motion parallax has a role in generating this phenomenon, the supporting data are equivocal. The current study proposed that the ambiguity regarding the role of motion parallax may have arisen because there are contradictions between relative size cues and motion parallax cues in the configuration of rotating circles. However, with 17 undergraduate observers, apparent depth was no more reliably reported with consistent cues of motion parallax and relative size than when these cues were contradictory.

Adult↗

Stereophotometric testing for Pulfrich's phenomenon in professional baseball players.

Major League players were significantly more accurate in performing stereophotometry than were Minor League players. The stereophotometric data based upon the induction and extinction thresholds of the Pulfrich phenomenon were significantly correlated with the batting averages of Major League baseball players. The coefficient of determination, r2, implies that visual ability as measured by stereophotometry accounts for 47% or more of the variation in batting averages of the Major League players. This test may be a useful index in predicting batting ability.

Adult↗

Stereokinetic interaction effects involving static and slowly moving identical figures.

Here a new depth effect evoked by the spatial and temporal interaction in 2-D of a slowly moving circle (optimally at 0.6 rads/sec) with an identical static circle is reported. Typically, respondents report that with increasing adjacency, commencing with separations of a few diameters, the moving circle appears in a different plane of depth to the static circle, it then usually appears to "dip" onto the static circle and after complete coincidence with it to rise away from it. This effect, together with a number of associated descriptions are commented upon, in addition to observations when viewing overlapped static circles and overlapped circles in motion, this latter stimulus condition evoking the stereokinetic effect. The authors have previously suggested that contour "sliding," which simulates motion parallax, is the key to understanding stereokinesis. The stimulus conditions giving rise to this new effect directly simulate the motion parallax information present in a retinal image.

Adolescent↗

Synchronization, decrease in strength of pattern, illusory contours, and neon-color effect.

When certain elements in a pattern are replaced by colored lines, a spreading of neon-like color can be seen around the lines. Using a variety of neon displaying patterns, we hypothesize that two conditions are critical to the neon effect. One is the occurrence of illusory contours and another a decrease in strength of pattern of the colored lines. On the basis of the two conditions, various phenomena of the neon effect are discussed. Finally, examining the striking characteristics of the neon effect, the vagueness of the colored lines and the spreading of the color of the colored lines over an illusory area wherein the color stimulus does not exist, we conclude that the neon effect is caused by synchronization of strength of pattern.

Color Perception↗