Mq. Mchenry et De. Angelaki, Primate translational vestibuloocular reflexes. II. Version and vergence responses to fore-aft motion, J NEUROPHYS, 83(3), 2000, pp. 1648-1661
Primate translational vestibuloocular reflexes. II. Version and vergence re
sponses to fore-aft motion. J. Neurophysiol. 83: 1648-1661, 2000. To mainta
in binocular fixation on near targets during fore-aft translational disturb
ances, largely disjunctive eye movements are elicited the amplitude and dir
ection of which should be tuned to the horizontal and vertical eccentriciti
es of the target. The eye movements generated during this task have been in
vestigated here as trained rhesus monkeys fixated isovergence targets at di
fferent horizontal and vertical eccentricities during 10 Hz fore-aft oscill
ations. The elicited eye movements complied with the geometric requirements
for binocular fixation, although not ideally. First, the corresponding ver
gence angle for which the movement of each eye would be compensatory was co
nsistently less than that dictated by the actual fixation parameters. Secon
d, the eye position with zero sensitivity to translation was not straight a
head, as geometrically required, but rather exhibited a systematic dependen
ce on viewing distance and vergence angle. Third, responses were asymmetric
, with gains being larger for abducting and downward compared with adductin
g and upward gaze directions, respectively. As frequency was varied between
4 and 12 Hz, responses exhibited high-pass filter properties with signific
ant differences between abduction and adduction responses. As a result of t
hese differences, vergence sensitivity increased as a function of frequency
with a steeper slope than that of version. Despite largely undercompensato
ry version responses, vergence sensitivity was closer to ideal. Moreover, t
he observed dependence of vergence sensitivity on vergence angle, which was
varied between 2.5 and 10 MA, was largely linear rather than quadratic (as
geometrically predicted). We conclude that the spatial tuning of eye veloc
ity sensitivity as a function of gaze and viewing distance follows the gene
ral geometric dependencies required for the maintenance of foveal visual ac
uity. However, systematic deviations from ideal behavior exist that might r
eflect asymmetric processing of abduction/adduction responses perhaps becau
se of different functional dependencies of version and vergence eye movemen
t components during translation.