It is well known that, typically, saccadic eye movements precede goal-direc
ted hand movements to a visual target stimulus. Also pointing in general is
more accurate when the pointing target is gazed at. In this study, it is h
ypothesized that saccades are not only preceding pointing but that gaze als
o is stabilized during pointing in humans. Subjects, whose eye and pointing
movements were re corded, had to make a hand movement and a saccade to a f
irst target. Ar arm movement peak velocity, when the eyes are usually alrea
dy fixating the first target, a new target appeared. and subjects had to ma
ke a saccade toward it (dynamical trial type). In the statical trial type,
a new target was offered when pointing was just completed. In a control exp
eriment, a sequence of two saccades had to be made, with two different inte
rstimulus intervals (ISI), comparable with the ISIs found in the first expe
riment for dynamic and static trial types. In a third experiment, ocular fi
xation position and pointing target were dissociated, subjects pointed at n
ot fixated targets. The results showed that latencies of saccades toward th
e second target were on average 155 ms longer in the dynamic trial types, c
ompared with the static trial types. Saccades evoked during pointing appear
ed to be delayed with approximately the remaining deceleration time of the
pointing movement, resulting in "nonnal" residual saccadic reaction times (
RTs), measured from pointing movement offset to saccade movement onset. In
the control experiment, the latency of the second saccade was on average on
ly 79 ms larger when the two targets appeared with a short ISI compared wit
h trials with long ISIs. Therefore the saccadic refractory period cannot be
responsible for the substantially bigger delays that:were found in the fir
st experiment. The observed saccadic delay during pointing is modulated by
the distance between ocular fixation position and pointing target. The larg
est delays were found when the targets coincided, the smallest delays when
they were dissociated. In sum, our results provide evidence for an active s
accadic inhibition process. presumably to keep steady ocular fixation at a
pointing target and its surroundings. Possible neurophysiological substrate
s that might underlie the reported phenomena are discussed.