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PubMed2003

Correlation between stereoanomaly and perceived depth when disparity and motion interact in binocular matching.

The aim of this study was to find out to what extent binocular matching is facilitated by motion when stereoanomalous and normal subjects estimate the perceived depth of a 3-D stimulus containing excessive matching candidates. Thirty subjects viewed stimuli that consisted of bars uniformly distributed inside a volume. They judged the perceived depth-to-width ratio of the volume by adjusting the aspect ratio of an outline rectangle (a metrical 3-D task). Although there were large inter-subject differences in the depth perceived, the experimental results yielded a good correlation with stereoanomaly (the inability to distinguish disparities of different magnitudes and/or signs in part of the disparity spectrum). The results cannot be explained solely by depth-cue combination. Since up to 30% of the population is stereoanomalous, stereoscopic experiments would yield more informative results if subjects were first characterized with regard to their stereo capacities. Intriguingly, it was found that motion does not help to define disparities in subjects who are able to perceive depth-from-disparity in half of the disparity spectrum. These stereoanomalous subjects were found to rely completely on the motion signals. This suggests that the perception of volumetric depth in subjects with normal stereoscopic vision requires the joint processing of crossed and uncrossed disparities.

Depth Perception↗
PubMedDate not supplied

African American women. Disparities in health care.

Healthy People 2000 outlines a vision for attaining improved health care for all Americans. This vision is based on the belief that all people should have opportunities to attain adequate health care. For this to be a realistic goal, health service must move from traditional settings such as hospitals, clinics, and outpatient departments to neighborhood centers, schools, churches, workplace environments and homes. But as the settings become redefined, the populations needing the care must be better understood.

Adult↗
PubMed2003

Motion distorts perceived depth.

Two important tasks that the visual system has to perform are determining the direction of motion and the spatial location of objects. It has recently been shown that the perceived location of an object moving in the frontal-plane is displaced along the direction of motion (e.g. Nature 397 (1999) 610; Vision Research 31 (1991) 1619). The aim of the present study is to examine the extent of this interaction between motion and perceived location. The observers' task was to indicate which of two vertically separated moving stimuli was closer. The two stimuli were presented at various relative disparity offsets. The stimuli consisted of moving dot patterns (optic-flow) that simulated either fronto-parallel motion (all the dots moved one direction) or motion in depth. Motion of the dots towards the centre of the stimulus simulated object motion away from the observer and motion of the dots away from the centre of the stimulus simulated object motion towards the observer. Results indicate that motion-in-depth information can bias perceived stereoscopic-based depth. Simulated motion towards the observer made the object appear closer to the observer than the depth signalled by the disparity information and simulated motion away from the observer made it seem further away. The results of this study, when combined with those of previous studies, show that motion can distort our entire three dimensional representation of space.

Adaptation, Ocular↗
PubMed2003

At least at the level of inferior temporal cortex, the stereo correspondence problem is solved.

Stereoscopic vision requires the correspondence problem to be solved, i.e., discarding "false" matches between images of the two eyes, while keeping correct ones. To advance our understanding of the underlying neuronal mechanisms, we compared single neuron responses to correlated and anticorrelated random dot stereograms (RDSs). Inferior temporal neurons, which respond selectively to disparity-defined three-dimensional shapes, showed robust selectivity for correlated RDSs portraying concave or convex surfaces, but unlike neurons in areas V1, MT/V5, and MST, were not selective for anticorrelated RDSs. These results show that the correspondence problem is solved at least in far extrastriate cortex, as it is in the monkey's perception.

Animals↗
PubMed2001

Cortical mechanisms of binocular stereoscopic vision.

The early neurophysiology of binocular vision is largely dominated by measurements of disparity selectivity in cortical neurons in various visual areas. Incisive progress has been made by the intensive study of the mechanism of disparity selectivity of V1 in cortical neurons and the development of a number of tests for the involvement of single neurons in the perception of stereoscopic depth. The picture that now emerges is that cortical area V1 must be a preliminary processing stage for the analysis of stereoscopic depth, whereas some of the extrastriate areas may actually be responsible for the generation of neuronal signals that underlie the perception of binocular depth.

Animals↗
PubMed1985

Detection of binocular disparities.

A stereo correspondence algorithm designed to perform matching on figurally similar images (arising in normal human binocular vision) is described. It is based on the observation that the operational principles underlying biological stereo disparity detection seem to be extremely general and few in number instead of an extended set of specific "constraints". We identify one general characteristic of objects in the three dimensional world and use it to formulate a simple noniterative, parallel and local algorithm that successfully detects disparities generated by opaque as well as transparent surfaces.

Humans↗
PubMed1990

Stereo and motion cues in preattentive vision processing--some experiments with random-dot stereographic image sequences.

Low-level preattentive vision processing is of special interest since it seems the logical starting point of all vision processing. Exploration of the human visual processing system at this level is, however, extremely difficult, but can be facilitated by the use of stroboscopic presentation of sequences of random-dot stereograms, which contain only local spatial and temporal information and therefore limit the processing of these images to the low level. Four experiments are described in which such sequences were used to explore the relationships between various cues (optical flow, stereo disparity, and accretion and deletion of image points) at the low level. To study these relationships in more depth, especially the resolution of conflicting information among the cues, some of the image sequences presented information not usually encountered in 'natural' scenes. The results indicate that the processing of these cues is undertaken as a set of cooperative processes.

Attention↗
PubMed1995

Stereopsis, spatial frequency and retinal eccentricity.

Stereoscopic depth discrimination thresholds increase with retinal eccentricity and distance from the horopter. However, in contrast to spatial resolution, the effects of spatial frequency on stereo-thresholds in the periphery are unknown. For spatial vision, it is generally assumed that the retina is comprised of a series of overlapping spatial filter mechanisms and that there is a commensurate increase in spatial scale as a function of retinal eccentricity. If the same holds true for mechanisms sensitive to stereoscopic depth, then stereo-thresholds for low spatial frequency stereoscopic stimuli may remain relatively invariant across the visual field, while thresholds for relatively high spatial frequency stimuli would increase. To further understand the role of the disparity sensitive mechanisms involved in depth discrimination, increment depth discrimination thresholds for both crossed and uncrossed disparities were measured as a function of eccentricity for retinal locations up to 10.0 deg along the horizontal meridian. We found that stereoscopic depth discrimination thresholds, as a function of distance from the horopter, increased in an exponential manner irrespective of spatial frequency. Stereo-thresholds also increased as a function of retinal eccentricity, however, the rate of increase depended on the spatial frequency composition of the stimuli. Best stereo-thresholds for stimuli composed of low spatial frequencies remained relatively invariant for retinal eccentricities up to 10.0 deg, while thresholds for the high spatial frequency stimuli increased with eccentricity.

Depth Perception↗
PubMed2005

Visual localization of sounds.

Circumscribed hemispheric lesions in the right hemisphere have been shown to impair auditory spatial functions. Due to a strong crossmodal links that exist between vision and audition, in the present study, we have hypothesized that multisensory integration can play a specific role in recovery from spatial representational deficits. To this aim, a patient with severe auditory localization defect was asked to indicate verbally the spatial position where the sound was presented. The auditory targets were presented at different spatial locations, at 8 degrees, 24 degrees, 40 degrees, 56 degrees to either sides of the central fixation point. The task was performed either in a unimodal condition (i.e., only sounds were presented) or in crossmodal conditions (i.e., a visual stimulus was presented simultaneously to the auditory target). In the crossmodal conditions, the visual cue was presented either at the same spatial position as the sound or at 16 degrees or 32 degrees, nasal or temporal, of spatial disparity from the auditory target. The results showed that a visual stimulus strongly improves the patient's ability to localize the sounds, but only when it was presented in the same spatial position of the auditory target.

Acoustic Stimulation↗
PubMed1996

A canonical microfunction for learning perceptual invariances.

An unsupervised method is presented which permits a set of model neurons, or a microcircuit, to learn low-level vision tasks, such as the extraction of surface depth. Each micro-circuit implements a simple, generic strategy which is based on a key assumption: perceptually salient visual invariances, such as surface depth, vary smoothly over time. In the process of learning to extract smoothly varying invariances, each microcircuit maximises a microfunction. This is achieved by means of a learning rule which maximises the long-term variance of the state of a model neuron and simultaneously minimises its short-term variance. The learning rule involves a linear combination of anti-Hebbian and Hebbian weight changes, over short and long time scales, respectively. The method is demonstrated on a hyperacuity task: estimating subpixel stereo disparity from a temporal sequence of random-dot stereograms. After learning, the micro-circuit generalises, without additional learning, to previously unseen image sequences. It is proposed that the approach adopted here may be used to define a canonical microfunction, which can be used to learn many perceptually salient invariances.

Computer Simulation↗
PubMed2005

Houston AANCART best practices: from vision to synergy to reality.

The theme for the 2004 AANCART Academy, "Community Partnerships for Cancer Control: From Vision to Synergy to Reality", characterizes Best Practices for the Houston AANCART site. Researchers and community members share a common vision for addressing the cancer and health disparities that exist in our Asian community. They banded together synergistically to bring to reality the programs and projects that are enabling more Asian Americans to understand their risks for cancer, receive screening and education, and access treatment and survivorship support. Along the way, Houston AANCART was also able to conduct meaningful and relevant community-based participatory research and to train young Asian and other investigators in how to reach out to this community in a culturally sensitive and appropriate manner.

Asian↗
PubMed1992

Grief and rage: collective emotions in the politics of peace and the politics of gender in Israel.

Collective emotions of rage and grief dominate Israeli political discourses regarding the Middle East conflict. The weekly peace vigils of the Women in Black who protest the state's occupation of the West Bank and Gaza and the opposition which the vigils encounter, publicly display politicized collective emotions. In these weekly confrontations, grief and rage articulate intense contestations regarding the politics of peace as well as the politics of gender in Israel. Rage and grief unravel two drastically different visions of transcending national vulnerabilities and two disparate constructions of gender identity.

Emotions↗
PubMed2001

Fixation could simplify, not complicate, the interpretation of retinal flow.

The visual system must generate a reference frame to relate retinal images in spite of head and eye movements. We show how a reference frame for storing the visual direction and depth of points can be composed from the angles and changes in angles between pairs and triples of points. The representation has no unique origin in 3-D space nor a unique set of cardinal directions (basis vectors). We show how this relative representation could be built up over a series of fixations and for different directions of translation of the observer. Maintaining gaze on a point as the observer translates helps in building up this representation. In our model, retinal flow is divided into changes in eccentricity and changes in meridional angle. The latter, called 'polar angle disparities' for binocular viewing (Weinshall, 1990. Computer Vision Graphics and Image Processing, 49 222-241), can be used to recover the relief structure of the scene in a series of stages up to full Euclidean structure. We show how the direction of heading can be recovered by a similar series of stages.

Computer Simulation↗
PubMed2004

Re-visioning the spider woman archetype in Kiss of the Spider Woman.

The article examines the transformation of spider woman archetype from Manuel Puig's adaptation of his novel to a play, and other adaptations into a film and a musical. The paper examines how the archetype's image and function shift when 're-visioned' by various artists and performed in disparate social contexts.

Humans↗
PubMed1997

Postnatal development of binocular disparity sensitivity in neurons of the primate visual cortex.

In macaque monkeys, the age at which neurons in the primary visual cortex (V1) become sensitive to interocular image disparities, a prerequisite for stereopsis, is a matter of conjecture. To resolve this fundamental issue in binocular vision development, we measured the responsiveness of individual V1 neurons in anesthetized and paralyzed infant monkeys as a function of the relative, interocular, spatial phase of dichoptic sine-wave gratings. We found that an adult-like proportion of units were sensitive to interocular image disparity as early as the sixth postnatal day, several weeks before the onset age for stereopsis in monkeys. The ocular dominance distributions of cells in infant monkeys were also indistinguishable from those of adults. Thus, at or only a few days after birth, V1 neurons are capable of combining neural signals from the two eyes as in adults and are sensitive to interocular image disparities. However, the monocular spatial-frequency response properties of these disparity-sensitive units were immature, and their overall responsiveness was far lower than that in adults. During the first 4 postnatal weeks, both the spatial frequency response properties and the peak response amplitude rapidly improved, which resulted in a corresponding increase in the absolute sensitivity of individual units to interocular disparity. The results demonstrate that early binocular vision development in monkeys is not constrained by a paucity of disparity-sensitive V1 neurons but, instead, by the relative immaturity of the spatial response properties and the overall unresponsiveness of existing disparity-sensitive neurons.

Animals↗
PubMed1996

Motor and sensory fusion in monkeys: psychophysical measurements.

Motor and sensory fusion, the basic processes of binocularity, must be present for bifoveal fixation with true fusion and stereopsis during ordinary viewing. The characteristics of motor and sensory fusion have been established for patients with normal and subnormal binocular vision; the present report describes our psychophysical studies of these processes in the macaque monkey. Three recent investigations of motor and sensory fusion in monkeys are described. The studies involved: (1) the comparability of motor and sensory fusion in monkeys and humans with normal binocular vision, (2) the effects of an early period of abnormal binocular vision on motor and sensory fusion in monkeys, and (3) the contrast sensitivity for binocular disparity in monkeys with stereo-deficiencies. The results of these studies demonstrated an excellent homology between the normal binocular vision of monkeys and humans. We also found that a period of esotropia during infancy caused deficiencies in sensory fusion, but not motor fusion. In some monkeys, the sensory deficiency persisted over the entire range of binocular disparities that were compatible with stereopsis, while other subjects demonstrated normal stereo-sensitivity for the largest fusible binocular disparities. The stereo-deficiencies of these monkeys, along with other visual attributes, suggest that their binocular vision is a viable model for the binocularity of patients with subnormal binocular vision or the monofixation syndrome.

Animals↗
PubMed1981

Vergence eye movements made in response to spatial-frequency-filtered random-dot stereograms.

Vergence responses were recorded from practised observers viewing narrow-band spatial-frequency-filtered planar random-dot stereograms. It was found that low spatial frequencies of 1.75-3.5 cycles deg-1 could trigger appropriate vergence responses to larger disparities than could the relatively high spatial frequency of 7.0 cycles deg-1. Nevertheless, appropriate vergence shifts were observed reliably for spatial-frequency/disparity combinations well outside the range predicted by Marr and Poggio's (1979) model of stereo vision. It was also found that for large-disparity/high-spatial-frequency combinations which the subjects could not fuse, the vergence system went into oscillation with the eyes diverging and converging at a frequency of about 1.5 Hz and with an amplitude of about 10-20 min arc. Finally, it was demonstrated that when a prominent monocular cue was superimposed upon a large-disparity/high-spatial-frequency stereogram then a speedy vergence response occurred which resulted in successful fusion. This latter finding supports the hypothesis advanced earlier that monocular cues can facilitate stereopsis by triggering appropriate vergence shifts.

Eye Movements↗
PubMed1991

Stereo perception in callosal agenesis and partial callosotomy.

Stereoperception in two acallosal patients and two partial callosotomy patients was compared with that of three normal subjects. All three patients with the splenium missing, whether due to agenesis or surgical intervention, showed midline deficits and broadly similar profiles; namely, they made few uncrossed midline responses. The patient with partial callosal section but with the splenium almost totally spared performed better at the midline than in the periphery. All degrees of disconnection produced some overall loss of performance, confirming the results of Hamilton and Vermeire (In Two Hemispheres--One Brain, F. Lepore, M. Pitto and H. H. Jasper (Editors), pp. 315-333. Alan R. Liss Inc., New York, 1986) and Hamilton et al. (Suppl. Invest. Ophthal. Vis. Sci. 28, 294, 1987). The results are discussed in the context of earlier reports of human and animal studies of stereoperception. Bearing in mind reports of structural alterations in layer III of the striate cortex in acallosals (Shoumjra, K. et al. Brain Res. 93, 241-252, 1975. Also, Akert, K. et al. Trans. Am. Neurol. Assoc. 79, 151-153, 1954), it is speculated that the specific difficulties encountered by them in handling uncrossed disparities may be due to a marked reduction or absence of far neurones in acallosal brains (Poggio, G. F. and Poggio, T. Ann. Rev. Neurosci. 7, 379-412, 1984). The likely importance of the anterior commissure in the efficient integration of crossed disparity (near neurones) (Cowey, A. In Brain Mechanisms and Spatial Vision, D. Ingle (Editor), NATO Advanced Study Institute Series, Martinus Nijhoff, The Hague, 1985) is seen as a possible explanation of the acallosals relative success in making crossed disparity judgements. The variability of performance in normals documented by Hamilton and Vermeire (In Two Hemispheres--One Brain, F. Lepore, M. Pitto and H. H. Jasper (Editors), pp. 315-333. Alan R. Liss Inc., New York, 1986) and Hamilton et al. (Suppl. Invest. Ophthal. Vis. Sci. 28, 294, 1987) is, not surprisingly, even more marked amongst acallosals.

Adult↗