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Loes C J van Dam

Publications and source records attributed to Loes C J van Dam.

6 recordsLinked to original sources

Retinal image shifts, but not eye movements per se, cause alternations in awareness during binocular rivalry.

Particularly promising studies on visual awareness exploit a generally used perceptual bistability phenomenon, "binocular rivalry"--in which the two eyes' images alternately dominate--because it can dissociate the visual input from the perceptual output. To successfully study awareness, it is crucial to know the extent to which eye movements alter the input. Although there is convincing evidence that perceptual alternations can occur without eye movements, the literature on their exact role is mixed. Moreover, recent work has demonstrated that eye movements, first, correlate positively with perceptual alternations in binocular rivalry, and second, often accompany covert attention shifts (that were previously thought to be purely mental). Here, we asked whether eye movements cause perceptual alternations, and if so, whether it is either the execution of the eye movement or the resulting retinal image change that causes the alternation. Subjects viewed repetitive line patterns, enabling a distinction of saccades that did produce foveal image changes from those that did not. Subjects reported binocular rivalry alternations. We found that, although a saccade is not essential to initiate percept changes, the foveal image change resulting from a (micro)saccade is a deciding factor for percept dominance. We conclude that the foveal image must change to have a saccade cause a change in awareness. This sheds new light on the interaction between spatial attention shifts and perceptual alternations.

Awareness↗

The role of saccades in exerting voluntary control in perceptual and binocular rivalry.

We have investigated the role of saccades and fixation positions in two perceptual rivalry paradigms (slant rivalry and Necker cube) and in two binocular rivalry paradigms (grating and house-face rivalry), and we compared results obtained from two different voluntary control conditions (natural viewing and hold percept). We found that for binocular rivalry, rather than for perceptual rivalry, there is a marked positive temporal correlation between saccades and perceptual flips at about the moment of the flip. Across different voluntary control conditions the pattern of temporal correlation did not change (although the amount of correlation did frequently, but not always, change), indicating that subjects do not use different temporal eye movement schemes to exert voluntary control. Analysis of the fixation positions at about the moment of the flips indicates that the fixation position by itself does not determine the percept but that subjects prefer to fixate at different positions when asked to hold either of the different percepts.

Depth Perception↗

The role of (micro)saccades and blinks in perceptual bi-stability from slant rivalry.

We exposed the visual system to an ambiguous 3D slant rivalry stimulus consisting of a grid for which monocular (perspective) and binocular (disparity) cues independently specified a slant about a horizontal axis. When those cues specified similar slants, observers perceived a single slant. When the difference between the specified slants was large, observers alternatively perceived a perspective- or a disparity-dominated slant. Eye movement measurements revealed that there was no positive correlation between a perceptual flip and both saccades (microsaccades as well as larger saccades) and blinks that occurred prior to a perceptual flip. We also found that changes in horizontal vergence were not responsible for perceptual flips. Thus, eye movements were not essential to flip from one percept to the other. After the moment of a perceptual flip the occurrence probabilities of both saccades and blinks were reduced. The reduced probability of saccades mainly occurred for larger voluntary saccades, rather than for involuntary microsaccades. We suggest that the reduced probability of voluntary saccades reflects a reset of saccade planning.

Blinking↗

Stereoscopic matching and the aperture problem.

In order to perceive stereoscopic depth, the visual system must define binocular disparities. Consider an oblique line seen through an aperture formed by flanking occluders. Because the line is perceived behind the aperture, the line must have disparity relative to the aperture. What is the assigned disparity of the line in this aperture problem? To answer this question five observers adjusted the horizontal disparity of a probe until it was perceived at the same depth as the disparate line behind the aperture. The results show that, when both the horizontal and the vertical disparities of the occluders are well-defined, the probe must have the same horizontal disparity as the horizontal separation between the line half-images. However, when the horizontal and vertical disparities of the occluders are ill-defined, the intersections of the line and the occluder borders can determine the matching direction. In the latter case, the matching direction varies with the aperture orientation and there is considerable variability across observers.

Depth Perception↗

The influence of cyclovergence on unconstrained stereoscopic matching.

In order to perceive depth from binocular disparities the visual system has to identify matching features of the two retinal images. Normally, the assigned disparity is unambiguously determined by monocularly visible matching constraints. The assigned disparity is ambiguous when matching is unconstrained, such as when we view an isolated long oblique disparate line. Recently we found that in order to perceive a depth probe at the same depth as the oblique line, the probe needs to have the same horizontal disparity as the line (i.e. matching occurs along horizontal "search-zones" [Vis. Res. 40 (2000) 151]). Here we examined whether the depth probe disparity in unconstrained matching of long lines is influenced by cyclovergence, by cyclorotation between stereogram half-images, or by combinations of the two. We measured retinal rotation (>6 deg in cyclovergence conditions). We found that in those conditions in which the retinal images were the same (a condition with, say, both zero cyclovergence and zero cyclorotation between the half-images, creates the same retinal images as a condition with both 6 deg cyclovergence and 6 deg cyclorotation) assigned depth was the same too, i.e. independent of cyclovergence. Thus, the assigned depth of the test-line seems to be determined solely by the retinal test-line orientation, implying that the binocular matching algorithm does not seem to incorporate the eyes' cyclovergence when matching is unconstrained.

Depth Perception↗

Bi-stability in perceived slant when binocular disparity and monocular perspective specify different slants.

We examined how much depth we perceive when viewing a depiction of a slanted plane in which binocular disparity and monocular perspective provide different slant information. We exposed observers to a grid stimulus in which the monocular--and binocular-specified grid orientations were varied independently across stimulus presentations. The grids were slanted about the vertical axis and observers estimated the slant relative to the frontal plane. We were particularly interested in the metrical aspects of perceived slant for a broad spectrum of possible combinations of disparity--and perspective-specified slants. We found that observers perceived only one grid orientation when the two specified orientations were similar. More interestingly, when the monocular--and binocular-specified orientations were rather different, observers experienced perceptual bi-stability (they were able to select either a perspective--or a disparity-dominated percept).

Depth Perception↗