We investigated the dynamics of neurons in the striate cortex (V1) and
the lateral geniculate nucleus (LGN) to study the transformation in t
emporal-frequency tuning between the LGN and V1. Furthermore, we compa
red the temporal-frequency tuning of simple with that of complex cells
and direction-selective cells with nondirection-selective cells, in o
rder to determine whether there are significant differences in tempora
l-frequency tuning among distinct functional classes of cells within V
1. In addition, we compared the cells in the primary input layers of V
1 (4a, 4c alpha, and 4c beta) with cells in the layers that are predom
inantly second and higher order (2, 3, 4b, 5, and 6). We measured temp
oral-frequency responses to drifting sinusoidal gratings. For LGN neur
ons and simple cells, we used the amplitude and phase of the fundament
al response. For complex cells, the elevation of impulse rate (FO) to
a drifting grating was the response measure. There is significant low-
pass filtering between the LGN and the input layers of V1 accompanied
by a small, 3-ms increase in visual delay. There is further low-pass f
iltering between V1 input layers and the second- and higher-order neur
ons in V1. This results in an average decrease in high cutoff temporal
-frequency between the LGN and V1 output layers of about 20 Hz and an
increase in average visual latency of about 12-14 ms. One of the most
salient results is the increased diversity of the dynamic properties s
een in V1 when compared to the cells of the lateral geniculate, possib
ly reflecting specialization of function among cells in V1. Simple and
complex cells had distributions of temporal-frequency tuning properti
es that were similar to each other. Direction-selective and nondirecti
on-selective cells had similar preferred and high cutoff temporal freq
uencies, but direction-selective cells were almost exclusively band-pa
ss while nondirection-selective cells distributed equally between band
-pass and low-pass categories. Integration time, a measure of visual d
elay, was about 10 ms longer for V1 than LGN. In V1 there was a relati
vely broad distribution of integration times from 40-80 ms for simple
cells and 60-100 ms for complex cells while in the LGN the distributio
n was narrower.