Journal of Neuroscience, Vol 12, 2247-2250, Copyright © 1992 by Society for Neuroscience
ON- and OFF-pathways form separate neural substrates for motion perception: psychophysical evidence
C Wehrhahn and D Rapf
Max-Planck-Institut fur biologische Kybernetik, Tubingen, Germany.
We have tested the hypothesis that in humans the signals carried by ON- and
OFF-pathway respectively are processed for the perception of motion by two
distinct physiological substrates. In vertebrates, onset of a bright visual
stimulus is signaled to the CNS by ON-center retinal ganglion cells; onset
of a dark stimulus is transmitted by OFF-center cells. We chose apparent
motion generated by successive presentation of two adjacent lines as a
stimulus. Lines presented on a bright background were either darker or
brighter than this background. Delayed onset of a pair of bright or dark
lines elicits apparent motion at the same time fulfilling the constraint of
stimulating either ON- or OFF- center ganglion cells, respectively. We
determined the threshold delay needed for subjects to perceive the temporal
order of the onset of the two lines for various angular separations. The
threshold delay for a pair of bright lines stayed low for separations from
2' to 7'. The threshold delay for a pair of dark lines was low only within
a narrow range of separations centered around 3'. The variation of
thresholds with line distance must reflect the existence of a limited
processing zone for the perception of motion. The diameter of the
processing zone for bright lines is about twice as large as that for dark
lines. This suggests that in humans the separation of ON- and OFF-pathways
extends to the early stages of motion perception. To test this hypothesis
independently, thresholds were determined when a bright and a dark line
were presented in succession. This was done for a separation of 3' where
thresholds for a pair of lines with equal contrast are similarly low.
Temporal order was perceived correctly only when the delay was at least two
to four times as high as the threshold delays found for the equal contrast
stimuli.