The visual system tends to assign contrast borders to one of the adjacent
regions as if they were contours of objects in 3D space. Without proper 3D
information this assignment is generally ambiguous, as demonstrated by Rubin's
vase figure (see left). Zhou, Friedman & von der
Heydt (2000) have shown that many neurons in
areas V1, V2, and V4 respond differently to contrast defined borders when these
borders are displayed as part of visual objects on different sides (see
Figure
side selectivity), where the edge in the receptive field (ellipse) is the bottom
left side of a square in A and C, but the top right side of a square in B and D.
The cell shown here prefers the figure to be on the lower left of the RF
irrespective of the contrast polarity. These findings suggested that neurons in
these regions encode perceptual border ownership. The crucial test of this
hypothesis is to examine the responses of orientation-selective V2 cells to
contrast-defined and disparity-defined figures. A contrast-defined square is
generally perceived as "figure", with the borders assigned to the square (see
Figure side selectivity) while a corresponding
region in a random-dot stereogram is perceived either as a "figure", if its
disparity is "near", or as a "window", if its disparity is "far", relative to
that of the surrounding region. In the stereogram, the nearer surface always
owns the border. In this study we examine whether
the figure side preference of neurons depends on disparity in the same way (see
Stereograms).
Cells that signal edges in random-dot stereograms exist in
V2 (von der Heydt, Zhou & Friedman, 2000) (see
Stereoscopic edge selectivity). If our
hypothesis is correct, the disparity cue should override other figure ground
cues such as convexity and size.