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At least 1,135 records · Page 63Linked to original sources
PubMed1999

How stereovision interacts with optic flow perception: neural mechanisms.

Optic flow, the global visual motion experienced during self-movement, supplies important navigational information. Optic flow analysis in the visual system is aided by several other visual and non-visual signals. Recent psychophysical findings demonstrate an interaction of optic flow perception and stereoscopic depth vision. Retinal disparity strongly affects an optic flow illusion, which can be related to the mechanisms of visual self-motion detection. To investigate the neuronal basis of this interaction, we tested several hypotheses by introducing different disparity contributions in a detailed neurobiological model of optic flow processing in monkey cortex. The disparity-dependent modification, which accounted best for the data suggests a specific contribution of a subset of stereoscopically modulated cortical neurons present in areas MT and MST.

Journal Article↗
PubMed2003

Visual motion retards alternations between conflicting perceptual interpretations.

When the visual system is faced with conflicting or ambiguous stimulus information, visual perception fluctuates over time. We found that perceptual alternations are slowed when inducing stimuli move within the visual field, constantly engaging fresh, unadapted neural tissue. During binocular rivalry, dominance durations were longer when rival figures moved compared to when they were stationary, yielding lower alternation rates. Rate was not reduced, however, when observers tracked the moving targets, keeping the images on approximately the same retinal area. Alternations were reliably triggered when rival targets passed through a local region of the visual field preadapted to one of the rival targets. During viewing of a kinetic globe whose direction of rotation was ambiguous, observers experienced fewer alternations in perceived direction when the globe moved around the visual field or when the globe's axis of rotation changed continuously. Evidently, local neural adaptation is a key ingredient in the instability of perception.

Humans↗
PubMed1997

Binocular rivalry: ambiguities resolved.

For over 100 years, binocular rivalry was seen as the result of competition between the two eyes, involving reciprocal suppression of retinal inputs. Now it emerges that rivalry reflects alternating perceptual interpretations that are represented in the firing patterns of cells in the temporal visual cortex.

Animals↗
PubMed1990

A physiological model of binocular rivalry.

This paper presents a modified reciprocal inhibition model for the temporal dynamics of binocular rivalry. The model is based on neurophysiological mechanisms and is derived from human psychophysical data. A simple reciprocal inhibition oscillator may be described with a set of four coupled differential equations with a neurophysiological interpretation. However, such a circuit does not account for some aspects of the temporal behavior of binocular rivalry, including the effects of contrast change on alternation rate and on the magnitudes of changes in duration of the suppressed and dominant phases. To better account for these phenomena, the equations and their stimulation are modified to include three new components: (1) presynaptic inhibition of the reciprocal inhibition by the input, (2) the motor delays that occur when a human observer tracks rivalry and (3) a minimum threshold for each neuron's state variable. The result is a much improved fit to psychophysically-obtained data on the temporal behavior of binocular rivalry. Finally, the model is incorporated into a larger model to suggest how rivalry might occur in a network that usually exhibits binocular fusion.

Contrast Sensitivity↗
PubMedDate not supplied

Psychophysical evidence for area V2 involvement in the reduction of subjective contour tilt aftereffects by binocular rivalry.

Previous research suggests binocular rivalry disrupts extrastriate, but not striate processes, although the locus along the visual pathway at which such disruption first occurs is uncertain. It has been argued that subjective contours arise via a two-stage process in which end-stopped cells feed into orientation-sensitive neurones in V2, and that orientation aftereffects induced with subjective contours are the product of mechanisms similar to those giving rise to real contour aftereffects. If binocular rivalry disrupts the acquisition of subjective contour aftereffects, then it follows from this model that rivalry disrupts processing in V2. Experiments reported here confirm this and provide evidence which suggests binocular rivalry arises through interactions between binocular neurones, rather than via some type of specialized binocular rivalry mechanism.

Afterimage↗
PubMedDate not supplied

Reduction of a pattern-induced motion aftereffect by binocular rivalry suggests the involvement of extrastriate mechanisms.

Previous research suggests that plaid-induced motion aftereffects (MAEs) involve extrastriate mechanisms (Wenderoth et al., 1988). There is evidence also that binocular rivalry occurs beyond V1 and that it disrupts the processing of MAEs which are believed to be based upon extrastriate mechanisms (e.g. the spiral MAE) but not MAEs, such as linear MAE induced by a drifting grating, which are thought to arise in striate cortex (Wiesenfelder & Blake, 1990). The logical inference is that binocular rivalry during drifting plaid-induced adaptation should reduce the MAEs which result. We report experiments which confirm this prediction.

Adaptation, Ocular↗
PubMed1992

Binocular rivalry suppression disrupts recovery from motion adaptation.

The motion aftereffect (MAE) lasts longer when the test period does not immediately follow adaptation, a phenomenon called storage. Does storage of the MAE occur if the test target is present but rendered phenomenally invisible owing to the presence of a rival target presented to the other eye during the storage period? Our experiment addressed this question. Following adaptation to a drifting grating, an intervening period preceded testing with a stationary grating. During this period, the adapted eye either viewed the test target immediately or was occluded, and the unadapted eye either viewed a high-contrast rival target or was occluded. Thus four conditions were employed. The duration of the residual MAE was found to be longer for the rivalry condition (grating and rival target viewed) than for the normal MAE condition (grating viewed), and comparable to that in the stored MAE condition (both eyes occluded). Thus, the MAE is stored when the test target is rendered invisible due to binocular rivalry, indicating that a suppressed target is ineffective at promoting decay of the MAE. So while suppression does not prevent information about the adapting grating from reaching the site of generation of the MAE (Lehmkuhle & Fox, 1975), it can prevent information about the test target from reaching the site of the stored MAE. Current models attribute the MAE to reduced responsiveness of direction-selective cortical neurons (Sutherland, 1961; Barlow & Hill, 1963). Thus, storage should reflect a differential return of these adapted cells to preadapted response levels, dependent on postadaptation stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)

Adaptation, Ocular↗
PubMed1991

Apparent extended body motions in depth.

Five experiments were designed to investigate the influence of three-dimensional (3-D) orientation change on apparent motion. Projections of an orientation-specific 3-D object were sequentially flashed in different locations and at different orientations. Such an occurrence could be resolved by perceiving a rotational motion in depth around an axis external to the object. Consistent with this proposal, it was found that observers perceived curved paths in depth. Although the magnitude of perceived trajectory curvature often fell short of that required for rotational motions in depth (3-D circularity), judgments of the slant of the virtual plane on which apparent motions occurred were quite close to the predictions of a model that proposes circular paths in depth.

Adult↗
PubMed1992

Do recognizable figures enjoy an advantage in binocular rivalry?

Five experiments examined whether recognizable stimuli predominate in binocular rivalry. It was found that a face predominated more than did a pattern equated for spatial frequency, luminance, and contrast; an objective reaction time procedure confirmed predominance of the face. The face was still liable to fragmentation as stimulus size increased. Observers tracked exclusive dominance of a picture of a camouflaged figure (a Dalmatian dog) prior to and then following discovery of the figure's presence; control observers received the same protocol with a scrambled version of the dog stimulus. Compared with control results, predominance of the dog picture was higher even before observers knew of the camouflaged figure. Inversion of the dog figure reduced its predominance. Binocular rivalry is sensitive to object-related, configural properties of a stimulus.

Attention↗
PubMed1993

Depth perception in motion parallax and stereokinesis.

Perceived depth in the stereokinetic effect (SKE) illusion and in the monocular derivation of depth from motion parallax were compared. Motion parallax gradients of velocity can be decomposed into 2 components: object- and observer-relative transformations. SKE displays present only the object-relative component. Observers were asked to estimate the magnitude and near-far order of depth in motion parallax and SKE displays. Monocular derivation of depth magnitude from motion parallax is fully accounted for by the perceptual response to the SKE, and observer-relative transformations absent in the SKE are of perceptual utility only as determinants of the near-far signing of perceived sequential depth. The amount of depth and rigidity perceived in motion parallax and SKE displays covaries with the projective size of the stimuli. The monocular derivation of depth from motion is mediated by a perceptual heuristic of which the SKE is symptomatic.

Adult↗
PubMed1994

Stimulus-driven attentional capture: evidence from equiluminant visual objects.

Previous work has shown that abrupt visual onsets capture attention. Possible attention. Possible mechanisms for this phenomenon include (a) a luminance-change detection system and (b) a mechanism that detects the appearance of new perceptual objects. Experiments 1 and 2 revealed that attention is captured in visual search by the appearance of a new perceptual object even when the object is equiluminant with its background and thus exhibits no luminance change when it appears. Experiment 3 showed that a highly salient luminance increment alone is not sufficient to capture attention. These findings suggest that attentional capture is mediated by a mechanism that detects the appearance of new perceptual objects.

Attention↗
PubMed1997

Amodal completion of partly occluded surfaces: is there a mosaic stage?

Recent investigators have proposed that amodal completion is a sequential process requiring a preliminary mosaic stage. Results of 6 studies of the time course of completion processes show support for this mosaic-first view with pictorial displays, but not with displays involving occlusion specified by binocular parallax or when pictorial displays were observed monocularly. These results still do not rule out the mosaic-first view. A parallel model, however, can account more economically for the available data.

Adult↗
PubMed2000

Distortions in definite distance and shape perception as measured by reaching without and with haptic feedback.

Psychophysical studies reveal distortions in perception of distance and shape. Are reaches calibrated to eliminate distortions? Participants reached to the front, side, or back of a target sphere. In Experiment 1, feedforward reaches yielded distortion and outward drift. In Experiment 2, haptic feedback corrected distortions and instability. In Experiment 3, feedforward reaches with only haptic experience of targets replicated the shape distortions but drifted inward. This showed that outward drift in Experiment 1 was visually driven. In Experiment 4, visually guided reaches were accurate when participants used binocular vision but when they used monocular vision, reaches were distorted. Haptic feedback corrected inaccuracy and instability of distance but did not correct monocular shape distortions. Dynamic binocular vision is representative and accurate and merits further study.

Adult↗
PubMed2002

The stereoscopic anisotropy: individual differences and underlying mechanisms.

Observers are more sensitive to variations in the depth of stereoscopic surfaces in a vertical than in a horizontal direction; however, there are large individual differences in this anisotropy. The authors measured discrimination thresholds for surfaces slanted about a vertical axis or inclined about a horizontal axis for 50 observers. Orientation and spatial frequency discrimination thresholds were also measured. For most observers, thresholds were lower for inclination than for slant and lower for orientation than for spatial frequency. There was a positive correlation between the 2 anisotropies, resulting from positive correlations between (a) orientation and inclination thresholds and (b) spatial frequency and slant thresholds. These results support the notion that surface inclination and slant perception is in part limited by the sensitivity of orientation and spatial frequency mechanisms.

Anisotropy↗
PubMed2002

Perceiving motion while moving: how pairwise nominal invariants make optical flow cohere.

Computer-generated sequences simulated observer movement toward 10 randomly placed poles, 1 moving and 9 stationary. When observers judged their direction of movement, or heading, they used 3 related invariants: The (a) convergence and (b) decelerating divergence of any 2 poles specified that heading was to the outside of the nearer pole, and the (c) crossover of 2 poles specified that heading was to the outside of the farther pole. With all poles stationary, the field of 45 pairwise movements yielded a coherent specification of heading. With I pole moving with respect to the others, however, the field could yield an incoherent heading solution. Such incoherence was readily detectable; similar pole motion leading to coherent flow, however, was less readily detectable.

Adult↗
PubMed2000

Age-related changes in the control of attention in depth.

In 2 experiments, the authors examined the control of spatial attention in depth in advanced age. Observers viewed 2 sets of lines that overlapped in two-dimensional (2-D) space but that were presented at different depth locations. An exogenous cue indicated the depth at which a colored target line would appear. On some trials, a distracting colored element was also presented. The luminance of this distracter varied from high to low. For both older and younger adults, distractors slowed reaction time less if they were at a different depth from the target. This effect was more robust for older adults with low-luminance distractors, indicating an important role for target features as well as attentional control. Adding another feature (i.e., color) that distinguished between target and distracter reduced the effects of slowing shown by the older observers and eliminated the cost of low-luminance distractors for all observers. The results suggest that attentional control in depth is maintained in aging.

Adolescent↗
PubMed1995

Rotational and translational components of motion parallax: observers' sensitivity and implications for three-dimensional computer graphics.

The motion of objects during motion parallax can be decomposed into 2 observer-relative components: translation and rotation. The depth ratio of objects in the visual field is specified by the inverse ratio of their angular displacement (from translation) or equivalently by the inverse ratio of their rotations. Despite the equal mathematical status of these 2 information sources, it was predicted that observers would be far more sensitive to the translational than rotational component. Such a differential sensitivity is implicitly assumed by the computer graphics technique billboarding, in which 3-dimensional (3-D) objects are drawn as planar forms (i.e., billboards) maintained normal to the line of sight. In 3 experiments, observers were found to be consistently less sensitive to rotational anomalies. The implications of these findings for kinetic depth effect displays and billboarding techniques are discussed.

Adolescent↗