Adamovich S V, Berkinblit M B, Fookson O, Poizner H
Center for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ 07102, USA.
Exp Brain Res. 1999 Mar;125(2):200-10. doi: 10.1007/s002210050674.
The accuracy of visually guided pointing movements decreases with speed. We have shown that for movements to a visually defined remembered target, the variability of the final arm endpoint position does not depend on movement speed. We put forward a hypothesis that this observation can be explained by suggesting that movements directed at remembered targets are produced without ongoing corrections. In the present study, this hypothesis was tested for pointing movements in 3D space to kinesthetically defined remembered targets. Passive versus active acquisition of kinesthetic information was contrasted. Pointing errors, movement kinematics, and joint-angle coordination were analyzed. The movements were performed at a slow speed (average peak tangential velocity of about 1.2 m/s) and at a fast speed (2.7 m/s). No visual feedback was allowed during the target presentation or the movement. Variability in the final position of the arm endpoint did not increase with speed in either the active or the passive condition. Variability in the final values of the arm-orientation angles determining the position of the forearm and of the upper arm in space was also speed invariant. This invariance occurred despite the fact that angular velocities increased by a factor of two for all the angles involved. The speed-invariant variability supports the hypothesis that there is an absence of ongoing corrections for movements to remembered targets: in the case of a slower movement, where there is more time for movement correction, the final arm endpoint variability did not decrease. In contrast to variability in the final endpoint position, the variability in the peak tangential acceleration increased significantly with movement speed. This may imply that the nervous system adopts one of two strategies: either the final endpoint position is not encoded in terms of muscle torques or there is a special on-line mechanism that adjusts movement deceleration according to the muscle-torque variability at the initial stage of the movement. The final endpoint position was on average farther from the shoulder than the target. Constant radial-distance errors were speed dependent in both the active and the passive conditions. In the fast speed conditions, the radial distance overshoots of the targets increased. This increase in radial-distance overshoot with movement speed can be explained by the hypothesis that the final arm position is not predetermined in these experimental conditions, but is defined during the movement by a feedforward or feedback mechanism with an internal delay.
视觉引导的指向运动的准确性会随着速度降低。我们已经表明,对于指向视觉定义的记忆目标的运动,最终手臂端点位置的变异性并不取决于运动速度。我们提出了一个假设,即这种观察结果可以通过表明指向记忆目标的运动是在没有持续校正的情况下产生的来解释。在本研究中,针对在三维空间中指向动觉定义的记忆目标的指向运动对该假设进行了测试。对比了动觉信息的被动获取与主动获取。分析了指向误差、运动运动学和关节角度协调。运动以慢速(平均峰值切向速度约为1.2米/秒)和快速(2.7米/秒)进行。在目标呈现或运动过程中不允许有视觉反馈。在主动或被动条件下,手臂端点最终位置的变异性均不会随速度增加。确定前臂和上臂在空间中位置的手臂定向角度最终值的变异性也是速度不变的。尽管所有涉及角度的角速度都增加了两倍,但这种不变性仍然存在。速度不变的变异性支持了这样的假设,即指向记忆目标的运动不存在持续校正:在运动较慢的情况下,有更多时间进行运动校正,但最终手臂端点的变异性并未降低。与最终端点位置的变异性相反,峰值切向加速度的变异性随着运动速度显著增加。这可能意味着神经系统采用了两种策略之一:要么最终端点位置不是根据肌肉扭矩进行编码,要么存在一种特殊的在线机制,在运动初始阶段根据肌肉扭矩变异性来调整运动减速。最终端点位置平均比目标离肩部更远。在主动和被动条件下,恒定的径向距离误差均与速度有关。在快速条件下,目标的径向距离超调增加。这种随着运动速度增加的径向距离超调可以通过以下假设来解释:在这些实验条件下,最终手臂位置不是预先确定的,而是在运动过程中由具有内部延迟的前馈或反馈机制定义的。