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Binocular-disparity-dependent upper-lower hemifield anisotropy and left-right hemifield isotropy as revealed by dynamic random-dot stereograms.

Dynamic random-dot stereograms devoid of all monocular depth cues were used to measure the limits of temporal and spatial resolution in the center of the visual field. The temporal durations for detecting a small, briefly presented test square of different binocular disparity than the surround varied as a function of its location and binocular disparity. The test squares presented in the upper hemifield were detectable at consistently shorter durations than those presented in the lower hemifield for a surround disparity which was uncrossed relative to the fixation marker. For crossed surround disparity this preference reversed, resulting in a superiority of the lower hemifield. The anisotropy diminished for zero surround disparity. No such anisotropy was found when left and right visual hemifields were compared. It was also shown that this upper-lower temporal anisotropy (and left-right isotropy) is paralleled by a similar disparity-dependent upper-lower anistropy (and left-right isotropy) in spatial resolution. Introduction of monocular clues into the stereograms tended to eliminate the anisotropies. This implies that the anisotropies reflect the spatiotemporal properties and distribution of binocular disparity detectors in the human cortex and result in a tilted surface that pivots around the horizontal midline in the space of binocular depth perception.

Depth Perception↗

The role of monocular regions in stereoscopic displays.

Random-dot stereograms of an object standing out from a background always contain a monocular region at the side of the foreground object. This is equivalent to the monocularly occluded part of the background in the real-life viewing of one object in front of another. The role of these monocular regions in the stereoscopic process has not been investigated previously, although it is generally assumed that they are a source of difficulty in stereoscopic resolution because of the unmatchable texture within them. The basis of the present study was a prediction that the presence of texture within these regions would facilitate rather than retard stereoscopic processing. This prediction follows from a hypothesis that stereoscopic processing is initially located at disparity discontinuities. Unmatched regions are only found at such discontinuities, and could serve to locate them.

Attention↗

Sensitivity to horizontal and vertical disparity and orientation preference in areas V1 and V2 of the monkey.

It has been suggested that cells are most sensitive to disparities along the axis orthogonal to their orientation preference. To test this assumption we studied the orientation preference of 73 cells sensitive to retinal disparity, 44 from V1 and 29 from V2. Orientation preference and disparity sensitivity were not related in tuned excitatory and tuned inhibitory cells. We found 18 near/far cells with orientation preference. Of these, 10 (56%) had a preferred orientation less than 30% away from the orthogonal to the disparity axis whereas the remaining eight cells (44%) exceeded this value. Our data suggests that the neural mechanisms for encoding retinal disparities present in dynamic random dot stereograms may not be related to the preferred orientation of the cell.

Animals↗

Coding of horizontal disparity and velocity by MT neurons in the alert macaque.

We performed the first large-scale (n = 501), quantitative study of horizontal disparity tuning in the middle temporal (MT) visual area of alert, fixating macaque monkeys. Using random-dot stereograms, we quantified the direction tuning, speed tuning, horizontal disparity tuning, and size tuning of each neuron. The vast majority (93%) of MT neurons were significantly tuned for horizontal disparity. Although disparity tuning was generally quite robust, the average disparity sensitivity of MT neurons was significantly weaker than their direction or speed sensitivity as quantified using both an index of response modulation and an index of signal-to-noise ratio. Disparity tuning was not correlated with direction or size tuning but tended to be broader and weaker for neurons that preferred faster speeds of motion. By comparison with recent studies, we find that disparity selectivity in MT is substantially stronger than that seen in either primary visual cortex (V1) or area V4. In addition, MT neurons are more broadly tuned for disparity than V1 neurons at comparable eccentricities. Disparity tuning curves are very well described by Gabor functions for >80% of MT neurons. The distribution of Gabor phases shows clear bimodality, indicating that MT neurons tend to have odd-symmetric disparity tuning (unlike neurons in V1). The preferred disparities were more strongly correlated with the phase parameter of the Gabor function than with the positional offset parameter. In fact, for neurons with preferred disparities close to zero, the positional offset tended to oppose the phase shift in specifying the disparity preference. We suggest that this result reflects a strategy used to finely distribute the disparity preferences of MT neurons, given the predominance of odd-symmetry and broad tuning.

Action Potentials↗

A comparison of two fixation disparity targets.

A simple homemade fixation disparity test is compared with the standard Mallett Test. Sixty-four clinical patients were tested and 25 percent of them were found to have fixation disparity on either one or both tests. Age distribution is shown. Comparisons are made as to the direction of fixation disparity and magnitude of associated heterophoria found with each test.

Adolescent↗

[Prism correction in heterophoria].

Unlike heterotropia (= manifest strabismus), heterophoria (= latent strabismus) is not a primarily existing condition but is a reaction to an interruption of the sensory-motor feedback control system. The reaction consists of a deviation from the orthovergence position. Binocular vision causes a continuous calibration of the vergence position. This "orthophorisation" explains that in most persons, heterophoria differs only slightly from zero. Nevertheless, a small heterophoria is common (70-80% of the population). The need to compensate for heterophoria by sensory-motor fusion can cause asthenopic complaints, such as headaches with prolonged reading. Since a variety of other defects can lead to similar symptoms, a causal relationship with heterophoria can be assumed only after a thorough differential diagnosis. Prism spectacles or eye muscle surgery for heterophoria should be recommended only after prism trials in free space, which include yoked prisms as a placebo control. Heterophoria should be distinguished from "Winkelfehlsichtigkeit", which is a deviation from orthoposition that results from the "measuring and correcting methodology after H.-J. Haase" (MKH) and is based on the idea that fixation disparity, a minute deviation from orthovergence position, indicates an inability to overcome a larger "vergence angle at rest". Objective recordings have, however, revealed that the subjective tests with stereo cues applied in the MKH can mislead to the assumption of a fixation disparity although both eyes are aligned exactly to the fixation point. A trial conducted in the Netherlands concerning the therapy of asthenopic complaints showed no statistically significant advantage of prism spectacles determined with the MKH over conventional spectacles.

Asthenopia↗

Transparency and the uniqueness constraint in human and computer stereo vision.

The sensation of depth that is obtained with human binocular vision results from the differences in the projection of the world onto the two retinae. The process entails solving the problem of stereo correspondence, which involves choosing the correct matches between left and right image features. Many computational models of stereo vision assume a uniqueness constraint on stereo matching-that is, each feature identified in one image should eventually be matched with only one feature in the other image. This constraint would seem to be justified, as allowing non-unique matches would be tantamount to supposing that the scene entities to which matches relate are in two places at once. The value of the uniqueness constraint for eliminating false matches has been demonstrated in a variety of stereo algorithms. Yet on the basis of psychophysical results Weinshall concluded that it was not used by humans in dealing with certain types of ambiguous random-dot stereograms. We have now tested how Weinshall's stereograms are dealt with by PMF, a stereo algorithm which uses a unique-matches selection procedure in conjunction with a purely local similar-disparity support scheme. We found that PMF produces results that are closely analogous to the psychophysical results. This suggests that Weinshall's experiments should not be interpreted as evidence that the human stereo mechanism establishes non-unique matches.

Algorithms↗

Interocular suppression is gated by interocular feature matching.

We present a new form of contrast masking in which the target is a patch of low spatial frequency grating (0.46 c/deg) and the mask is a dark thin ring that surrounds the centre of the target patch. In matching and detection experiments we found little or no effect for binocular presentation of mask and test stimuli. But when mask and test were presented briefly (33 or 200 ms) to different eyes (dichoptic presentation), masking was substantial. In a 'half-binocular' condition the test stimulus was presented to one eye, but the mask stimulus was presented to both eyes with zero-disparity. This produced masking effects intermediate to those found in dichoptic and full-binocular conditions. We suggest that interocular feature matching can attenuate the potency of interocular suppression, but unlike in previous work (McKee, S. P., Bravo, M. J., Taylor, D. G., & Legge, G. E. (1994) Stereo matching precedes dichoptic masking. Vision Research, 34, 1047) we do not invoke a special role for depth perception.

Accommodation, Ocular↗

Contour integration across depth.

In order to investigate the extent of the local connections subserving contour integration across depth, we measured performance for detecting the continuity of a path of Gabor elements distributed in depth and embedded in a three-dimensional field of random background elements. The results show that performance cannot be explained in terms of monocular performance and that contour information is not limited to single disparity planes. Path detection does indeed involve the integration of information across different, very disparate depth planes. The rules which emerge are in general similar to that already described in the two-dimensional case in as far as orientation and disparity are important. Unlike the two-dimensional case, three-dimensional integration operates over relatively large three-dimensional distances.

Depth Perception↗

Border enhancement as a function of binocular fixation performance.

Traditionally, fixation disparity is measured by interocular vertical alignment of unfusable monocular targets. The disparity generally increases with forced ocular vergences, producing characteristic individual functions. This study explores a new method of monitoring binocular fixation performance; the method is based on the effect of the distance of the border stimulus from the foveal center on the lateral spread of border enhancement. That is, as this distance increases, the enhancement spread increases. It is found that, as increasing ocular vergence is applied, the enhancement also increases, in a manner resembling conventional fixation disparity measurements. However, some dissimilarities between the border enhancement functions and the conventional functions suggest that the directional values used as a basis for the latter undergo modifications.

Accommodation, Ocular↗

Short-latency visual stabilization mechanisms that help to compensate for translational disturbances of gaze.

Recent studies in primates have revealed short-latency visual tracking mechanisms that help to stabilize the eyes during translational disturbances of the observer, and so operate as backups to otolith-mediated vestibulo-ocular reflexes. One such mechanism generates version eye movements to help stabilize gaze when the moving observer looks off to one side, utilizing binocular disparity to help single out the images in the plane of fixation (ocular following). Two others generate vergence eye movements to help maintain binocular alignment on objects that lie ahead: one responds to the radial patterns of optic flow (radial-flow vergence) and the other to the changes in binocular parallax (disparity vergence). Accumulating evidence suggests that, despite their short latency, all are mediated by the medial superior temporal area of cortex.

Adaptation, Physiological↗

A comparison of various methods of treatment of amblyopia. A block study.

The results of conventional occlusion, minimal occlusion and CAM treatment in the management of amblyopia have been investigated in two disparate populations from Cambridge, England and Ankara, Turkey. Each of these methods of treatment was equally effective as an initial therapy. However, if one form of therapy was ineffective or only partially successful, then further improvement can be obtained by using an alternative method. A quarter of the patients showed no improvement in vision at all despite vigorous and active treatment. It is suggested that minimal occlusion should be the first method of treatment but if this fails either or both conventional occlusion and CAM treatment should be used and therapy should not be abandoned until all these methods have been attempted.

Age Factors↗

Binocularly driven neurons in the rostral part of the frog optic tectum.

Receptive field (RF) properties of binocular neurons lying in the rostral part of the optic tectum of the frog (Rana esculenta) were studied electrophysiologically using conventional visual stimuli. They were classified into five groups: group 1 neurons have indefinite RF; group 2 neurons are total-field (T6) neurons; group 3 neurons have RFs covering a quadrant of the frontal visual field; group 4 neurons resemble T1(1) and T1(3) subclasses described earlier; and finally group 5 neurons look like small-field binocular neurons and are called T7(B). Moreover, RF disparity measurements conducted in all groups suggest that group 4 neurons support the estimation of binocular distance. This problem is discussed.

Action Potentials↗

Isolated inferior rectus paresis secondary to a mesencephalic cavernous angioma.

PURPOSE: To report a case of recurrent binocular, vertical diplopia presenting as an isolated, unilateral inferior rectus paresis occurring in a patient with a mesencephalic tegmental cavernous angioma. METHOD: Case report. A 30-year-old man with recurrent vertical diplopia underwent neuro-ophthalmic examination, laboratory examination, pharmacologic testing, and magnetic resonance imaging and angiography. RESULTS: Magnetic resonance imaging disclosed a lesion in the mesencephalon consistent with a cavernous angioma. Magnetic resonance angiography was negative. CONCLUSIONS: Isolated inferior rectus paresis is a rare phenomenon. This unique case involved a patient with recurrent inferior rectus paresis secondary to a mesencephalic cavernous angioma. The disparity between the extent of the lesion and the neuro-ophthalmologic consequences is remarkable.

Adult↗

Three-dimensional reconstruction of the actin cytoskeleton from stereo images.

In eucaryotic cells, actin filaments are abundant components in the cytoskeleton where they form a complex three dimensional (3D) structural network that provides the cell with its shape and mechanical properties. However, understanding the structural and mechanical properties of actin filaments composing the cell cytoskeleton is often hampered by the inability to faithfully reconstruct the three-dimensional geometric relationships. This paper presents a vision-based reconstruction approach that automatically reconstitutes the three-dimensional structures of cytoskeletal polymers from stereo image pairs taken at the different tilt angles. The approach finds corresponding points between two images and recovers the depth information about the structures. The computational process consists of three major procedures: feature representation, stereo matching, and disparity refinement, implemented in a multi-resolution manner based on a coarse-to-fine strategy. The reconstruction depicts the three-dimensional structure of cytoskeletal polymers and their geometric relationships. New and useful information becomes available and allows quantitative analysis of the structure. Measurement of the cytoskeleton geometrical properties and the filament concentration in a defined volume are obtained by direct calculation.

Actins↗

Receptive fields of disparity-tuned simple cells in macaque V1.

Binocular simple cells in primary visual cortex (V1) are the first cells along the mammalian visual pathway to receive input from both eyes. Two models of how binocular simple cells could extract disparity information have been put forward. The phase-shift model proposes that the receptive fields in the two eyes have different subunit organizations, while the position-shift model proposes that they have different overall locations. In five fixating macaque monkeys, we recorded from 30 disparity-tuned simple cells that showed selectivity to the disparity in a random dot stereogram. High-resolution maps of the left and right eye receptive fields indicated that both phase and position shifts were common. Single cells usually showed a combination of the two, and the optimum disparity was best correlated with the sum of receptive field phase and position shift.

Animals↗

The interpretation of stereo-disparity information: the computation of surface orientation and depth.

Two methods for interpreting disparity information are described. Neither requires extraretinal information to scale for distance: one method uses horizontal disparities to solve for the viewing distance, the other uses the vertical disparities. Method 1 requires the assumption that the disparities derive from a locally planar surface. Then from the horizontal disparities measured at four retinal locations the viewing distance and the equation of local surface 'patch' can be obtained. Method 2 does not need this assumption. The vertical disparities are first used to obtain the values of the gaze and viewing distance. These are then used to interpret the horizontal disparity information. An algorithm implementing the methods has been tested and is found to be subject to a perceptual phenomenon known as the 'induced effect'.

Depth Perception↗

The backward inclination of a surface defined by empirical corresponding points.

Three experiments were conducted to investigate whether a locus of binocular correspondence extends eccentrically from the vertical horopter. In experiment 1, we investigated whether the backward inclination of the vertical horopter was manifested in the angle at which readers prefer to orient the page. All observers preferred a page inclined backwards to any other orientation. This backward inclination was less than predicted from previous psychophysical reports, however. In experiment 2, we investigated the extent of binocular correspondence, defined by minimal apparent interocular horizontal motion, in the central 24 deg of the binocular field. Our data define a planar surface inclined top-away from the observer as a locus from which psychophysical corresponding points are stimulated. In experiment 3, we measured vertical adjustments required to eliminate apparent vertical motion. Together, the pattern of results from experiments 2 and 3 is most consistent with a planar surface, inclined top-away from the observer. This is consistent with Helmholtz's account of the backward inclination of the vertical horopter and expands the locus of zero horizontal disparity from a single line in the median plane to eccentric loci extending at least +/- 12 deg in the central binocular field.

Humans↗