![]() |
"The Development of Optic Flow Selectivity in MSTd Neurons Using Back-Propagation Networks" |
![]() |
Scott A. Beardsley, Lucia M. Vaina & *Tomaso A. Poggio
Brain & Vision Research Laboratory
Department of Biomedical Engineering
Boston University
Boston MA 02215
USA
*Massachusetts Institute of Technology
Center for Biological and Computational Learning
Cambridge MA
USA
In neurophysiological experiments examining the responses of MSTd neurons
to visual motion components of optic flow stimuli in monkeys, Duffy &
Wurtz (1991) reported neurons with double-component (plano-radial and plano-circular)
and triple-component (plano-radial-circular) selectivities, while Graziano
et al. (1994) reported neurons selective to spiral optic flows. Here we
address the apparent disagreement of these reported findings under simulated
experimental conditions. To examine the development of optic flow selectivities
in the hidden units of a two-layer back propagation network, we constructed
to computational models by using different input layer formats. The first
simulation used a sparse optic flow. The input format consisted of eight
circular MT receptive fields placed in the MSTd receptive field such that
the MT receptive fields were radially symmetric without overlap. Each MT
receptive field corresponded to eight directionally selective MT neurons
which equally divided the directional vector space. The second simulation
used a dense optic flow.The input format consisted of 67 overlapping MT
receptive fields of normally distributed diameter placed pseudo randomly
in the MSTd receptive field. Each MT receptive field corresponded to 16
directionally selective MT neurons which equally divided the vector space.
The hidden units were classified as MSTd neurons whose receptive fields
were coincident and encompassed the MT receptive fields from the input
layer. The output layer of the network consisted of MSTd neurons whose
receptive fields were consistent with the hidden layer. To minimize the
effects of biasing, the output selectivities were designated as expansion,
contraction, clockwise rotation, and counterclockwise rotation (consistent
with MSTd selectivities found in both experiments). In both sets of simulations
we found hidden units whose selectivities were consistent with the visual
motion components of optic flow stimuli reported by Duffy & Wurtz and
Graziano et al.
Duffy, C. J. & Wurtz, R. H. (1991a). "Sensitivity of MST neurons to optic flow stimuli. I. A continuum of response selectivity to large-field stimuli", J. Neurophysiol. 65, 1329-1345.
Duffy, C. J. & Wurtz, R. H. (1991b). "Sensitivity of MST neurons to optic flow stimuli. II. Mechanisms of response selectivity revealed by small-field stimuli", J. Neurophysiol. 65, 1346-1359.
Graziano, M. S. A., Anderson, R.
A. & Snowden, R. J. (1994). "Tuning of MST neurons to spiral motions",
J. Neuroscience 14, 54-67.