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Biomedical subjects

D C Shapiro

Publications and source records attributed to D C Shapiro.

6 recordsLinked to original sources

Summary knowledge of results for skill acquisition: support for the guidance hypothesis.

Summary knowledge of results (KR) involves the presentation KR for each of a set of trials (e.g., 10) only after the last trial in the set has been completed. Earlier, Lavery (1962) showed that, relative to providing KR after each trial, a 20-trial summary KR was detrimental to performance in a practice phase with KR present but was beneficial for a no-KR retention test. Using a relatively simple ballistic-timing task, we examined summary lengths of 1 (essentially KR after every trial), 5, 10, and 15 trials, searching for an inverted-U relationship between summary length and retention performance as predicated by a guidance hypothesis for KR. During acquisition when KR was present and being manipulated, all groups showed improvements in performance across practice, while increased summary lengths generally depressed performance. However, in a delayed no-KR retention test, there was an inverse relation between the summary length in acquisition and absolute constant error on the retention test. A guidance hypothesis is favored to explain how, relative to immediate KR, long KR summaries can provide detrimental effects in acquisition while enhancing retention performance.

Adult↗

The coordination of limb movements with different kinematic patterns.

The principles underlying the coordination of limb movements with different spatiotemporal features were explored. After an initial training session in which the same unidirectional movement had to be performed with both upper limbs, subjects attempted to coordinate two different movements in a second session, i.e., the learned unidirectional movement in the left limb and a new double reversal movement in the right limb. The findings uncovered a wide variety in patterns of interlimb dependence among and within subjects, going from a high degree of dependence to relative independence. The relationship between limbs was studied by means of a detailed analysis of the displacement and acceleration patterns and the electromyographic activity of the major muscles involved. The general underlying principle that appeared to account for the diversity in movement organization was this: higher independence between limb movements is achieved when subjects initiate the movements to be coordinated successively. This asynchrony in movement onset can possibly be viewed as an attempt to safeguard against interference.

Acceleration↗

Control of sequential movements: evidence for generalized motor programs.

The neuromotor processes underlying the control of rapid sequential limb movements were investigated. Subjects learned to pronate and supinate their forearms rapidly to four target locations in a specific spatio-temporal pattern under two movement-time conditions. The response sequence was first performed in a total movement time of 600 ms. Subjects were then told to produce the movement as quickly as possible while ignoring any timing pattern that they had previously learned. Electromyographic (EMG) signals were recorded from the biceps brachii and pronator teres muscles. Kinematic and EMG analyses were performed to investigate the temporal characteristics underlying the two movement-time conditions. When subjects produced the response as quickly as possible, average movement time to perform each reversal movement decreased while average peak velocity increased. Average total movement time was reduced by approximately 100 ms. Although movement time decreased, the proportion of total time to perform each movement of the sequence remained essentially invariant between movement-time conditions. Similar results were obtained for velocity. The time at which peak velocity was achieved occurred earlier in absolute time, although when normalized to the proportion of total movement time, the time to reach peak velocity was also invariant. Thus subjects proportionally compressed the entire movement sequence in time. The EMG analysis demonstrated that total EMG time decreased 89 ms on the average when subjects sped up the movement sequence. Thus average burst durations for both the biceps and pronator teres muscles decreased when movement speed increased. When burst durations were normalized to a proportion of total EMG time, the average proportion of time each muscle was active remained invariant. Therefore, the temporal pattern of activity for the biceps and pronator teres muscles were also proportionally compressed. The present experiment provided additional evidence for the structure of generalized motor programs consisting of invariant and variant features. Movement speed was considered a variant feature, which is specified each time the program is executed. Relative timing, the proportion of total time to produce each segment of the response, was considered to be an invariant feature and inherent in the structure of the motor program. Support for the invariance of relative timing was observed at both the kinematic and neuromuscular levels of analyses. Alternative models (9-11, 24) were found inadequate to account for the invariance of relative timing with the variation in movement time observed in the present experiment.

Electromyography↗

Effects of a secondary task on the accuracy of single aiming movements.

Recently, Schmidt, Zelaznik, and Frank and Schmidt, Zelaznik, Hawkins, Frank, and Quinn have demonstrated that in rapid, single aiming movements, variability in the movement's kinetic requirements resulted in variability in the movement's amplitude. This new explanation of the speed-accuracy trade-off in motor control, however, does not predict or explain inaccuracy for slower movements (greater than 200 msec). In the two experiments reported, we demonstrate that the Schmidt et al. model can predict variability in slow aiming movements if attention is occupied with an additional task. Subjects were required to perform single aiming movements in either 500 (Experiment 1) or 200 (Experiment 2) msec. In both experiments, the movement amplitude (30, 45, 60, and 75 cm in Experiment 1, and 10, 20, and 30 cm in Experiment 2) and the probability of an auditory probe-reaction time (RT) task were manipulated. Results indicated that only when the movement time (MT) was 500 msec did the probe-RT task change the relationship between the effective target width and the movement's average velocity. This result extended the scope of the Schmidt et al. model to movements with a duration greater than 200 msec. In addition, it seems as though slow movements are controlled by attention-demanding mental processes.

Attention↗

Coordinating visual and kinaesthetic memory codes.

Four experiments examined the Connolly & Jones (1970) model which postulates that translation between modalities in the cross-modal paradigm occurs before storage in short-term memory. In general, the results provided no support for the translation notion. Delaying until the end of the retention interval knowledge of the reproduction mode failed to produce a matching performance decrement. Subjects were able to maintain the code of original presentation through the retention interval even when they did not expect reproduction to be in this mode. In addition, the asymmetry in the cross-modal matching of visual (V) and kinaesthetic (K) information, whereby K-V performance is more accurate than V-K performance, was found to occur only under certain visual display conditions. The implications of these findings for general models of cross-modal translation were discussed.

Cues↗