THE primate visual system incorporates a highly specialized subsystem
for the analysis of motion in the visual field(1-6). A key element of
this subsystem is the middle temporal (MT) cortical area, which contai
ns a majority of direction-selective neurons(1-3). MT neurons are also
selective for binocular disparity (depth), which is perplexing given
that they are not sensitive to motion through depth(7). What is the ro
le of disparity in MT? Our data suggest an important link between disp
arity and transparent motion detection. Motion signals in different di
rections tend to inhibit each other within a given MT receptive field(
8). This inhibition has an averaging effect which minimizes MT respons
es to random motion signals created by light intensity changes and oth
er non-motion stimuli (motion noise)9. But, in the absence of disparit
y cues, inhibition may also occur between surfaces moving in different
directions through the same part of the visual field (transparent mot
ion), thus impairing the detection of either surface. Here we show tha
t inhibition in MT occurs mainly between motion signals with similar d
isparities. Transparent surface movements at different depths are thus
represented independently in MT (that is, without inhibiting each oth
er) whereas spurious motion signals from a given surface tend to cance
l out. To our knowledge, these results provide the first evidence for
a functional integration of motion and disparity in MT.