*G. P. KEITH1,5,
G. BLOHM5, J. D. CRAWFORD5,2,3,4
1Dept Psychol, 2Dept. of Psychology,
3Biol., 4Kinesiology, York Univ., Toronto, ON,
Canada; 5Ctr. for Vision Res., Toronto, ON, Canada
The frontal eye field, laterial
intraparietal area, and superior colliculus encode target positions in
eye-fixed spatial representations. These target positions must
therefore be updated across eye movements, and neurons in these brain
structures have shown remapping of activity across saccades. In a
topographically-organized structure such as the superior colliculus a
target position is represented as a hill of activity during each
fixation. It is currently unclear how this hill evolves during
remapping, however. We simulated target position remapping using
recurrent neural network models in order to examine how this evolution
depends on the signals that drive the remapping, the type of eye
movement, and the training condition. Eye movements considered were
saccades, pursuit movements, and a combination of these. The signals
used to drive the remapping in each case were efferent copies of the
3-D eye position (tonic) and velocity (burst) signals that control eye
movement. In the saccade paradigm, the 2-D saccade-target retinal
position signal in the superior colliculus was also considered. We
found that the activity representing target position evolved across
saccades as a slightly suppressed moving hill when the saccade-target
retinal position signal was not used to drive remapping, and as a
strongly suppressed jumping hill when this signal was used. In the
pursuit paradigm the pursuit target movements were of constant velocity
within each pursuit trial. We considered three pursuit training
conditions: one in which both the pursuit duration and velocity were
constant across all pursuit trials, one in which the velocity was
constant but the duration varied across pursuit trials, and one in
which velocity varied but duration was constant across trials. In all
cases the hill of activation representing target position evolved as a
moving hill during the pursuit movement. Only networks trained in the
constant-duration, constant-velocity condition, however, showed
significant suppression of this moving hill. In the
saccade-plus-pursuit paradigm, in which both pursuit duration and
velocity varied across trials, there was some suppression of activity
during remapping. When suppression is strong during remapping, a moving
hill resembles a jumping hill. The degree of suppression depends on the
behavioral condition and the spatiotemporal characteristics of the
signals used to drive the remapping.
Support Contributed By: CIHR (Canada). GB is supported by a Marie Curie
fellowship (EU) and by CIHR (Canada). JDC holds a Canada Research Chair.