Stereoscopic depth perception is based on binocular disparities. Although n
eurons in primary visual cortex (V1) are selective for binocular disparity,
their responses do not explicitly code perceived depth. The stereoscopic p
athway must therefore include additional processing beyond V1. We used func
tional magnetic resonance imaging (fMRI) to examine stereo processing in V1
and other areas of visual cortex. We created stereoscopic stimuli that por
trayed two planes of dots in depth, placed symmetrically about the plane of
fixation, or else asymmetrically with both planes either nearer or farther
than fixation. The interplane disparity was varied parametrically to deter
mine the stereoacuity threshold (the smallest detectable disparity) and the
upper depth limit (largest detectable disparity). fMRI was then used to qu
antify cortical activity across the entire range of detectable interplane d
isparities. Measured cortical activity covaried with psychophysical measure
s of stereoscopic depth perception. Activity increased as the interplane di
sparity increased above the stereoacuity threshold and dropped as interplan
e disparity approached the upper depth limit. From the fMRI data and an ass
umption that V1 encodes absolute retinal disparity, we predicted that the m
ean response of V1 neurons should be a bimodal function of disparity. A pos
t hoe analysis of electrophysiological recordings of single neurons in maca
ques revealed that, although the average firing rate was a bimodal function
of disparity (as predicted), the precise shape of the function cannot full
y explain the fMRI data. Although there was widespread activity within the
extrastriate cortex (consistent with electrophysiological recordings of sin
gle neurons), area V3A showed remarkable sensitivity to stereoscopic stimul
i, suggesting that neurons in V3A may play a special role in the stereo pat
hway.