Distance and movement time effects on the timing of agonist and antagonist muscles: a test of the impulse-timing theory

The experiment examined the effects of movement time (MT) and distance on the timing at electromyographic (EMG) activity from an agonist and antagonist muscle during rapid, discrete elbow movements in the horizontal plane. According to impulse-timing theory (Wallace, 1981) MT, not distance moved, should have a pronounced effect on the timing of EMG activity (duration of initial agonist and antagonist burst and time to onset of initial antagonist burst). The levels of MT were 100 and 160 msec and the levels of distance were 27 degrees and 45 degrees of elbow flexion. In general support of impulse-timing theory, the results of the three EMG timing measures showed that MT had a more pronounced effect on these measures than distance. In addition, the timing of EMG activity in relation to total MT remained fairly consistent across the four MT-distance conditions.     

Distance and Movement Time Effects on the Timing of Agonist and Antagonist Muscles

The experiment examined the effects of movement time (MT) and distance on the timing of electromyographic (EMG) activity from an agonist and antagonist muscle during rapid, discrete elbow movements in the horizontal plane. According to impulse-timing theory (Wallace, 1981) MT, not distance moved, should have a pronounced effect on the timing of EMG activity (duration of initial agonist and antagonist burst and time to onset of initial antagonist burst). The levels of MT were 100 and 160 msec and the levels of distance were 27° and 45° of elbow flexion. In general support of impulse-timing theory, the results of the three EMG timing measures showed that MT had a more pronounced effect on these measures than distance. In addition, the timing of EMG activity in relation to total MT remained fairly consistent across the four MT-distance conditions.     

The relation between preparatory stance and trunk rotation movements

The influence of preparatory stance on rotation movement reaction time of the trunk by bending of the knee and hip joint(s) was examined in 12 subjects. Four preparatory stances were examined: straight knee and hip extension (STAND), slight flexion of knee joints and hip joint (LIGHT), deep flexion (DEEP), and free initial position, i.e. that felt to be the most comfortable and effective (FREE). There was no significant influence of the preparatory stance on hip latency, but there were significant differences between the preparatory stances on response time (RT) and movement time (MT). Furthermore, using a quadratic curve fitting technique, knee joint angles of 24.8 degrees and a hip joint angle of 23.3 degrees were shown to be the optimum flexion angles in the preparatory stance for the initiation of quick trunk rotation movements. It is proposed that mechanical factors have considerably more effects on trunk rotation movements than does the nervous system.     

Effects of moment of inertia on simple reaction time

Two experiments examined the effect of altering the moment of inertia within an anatomical unit on simple reaction time (SRT), premotor time (PMT), and motor time (MOT) during the initiation of a discrete rapid movement. In Experiment 1 (N = 14), moment of inertia of the forearm was increased with the addition of a weighted cuff fastened around the wrist. In Experiment 2 (N = 7), moment of inertia was altered by the addition of a weighted sleeve to the index finger prior to rapid extension of the digit. Results from both experiments were unequivocal. An increase in the moment of inertia resulted in a significant increase in SRT and MOT but had no significant effect on PMT. Within selected anatomical unites (forearm and index finger), an increase in the moment of inertia does not appear to require additional neuromotor programming time but does influence the overall duration of response initiation.     

Fractioned Reaction Ttme in Power-Trained and Endurance-Trained Athletes under Conditions of Fatiguing Isometric Exercise

Fractionated knee extensor and plantar flexor reaction time (RT) components were assessed in a group of eight weightlifters and eight long distance runners. Following a 4-day period of baseline stabilization for each muscle group, a 50% maximal voluntary contraction (MVC) holding-time exercise was administered. Results showed that the runners had longer premotor times (PMT) than the weightlifters in the knee extensors, but had much faster PMTs than the lifters in the plantar flexor condition. Compared to previously reported investigations using non-athletes, the data for the present sample of athletes indicated faster total reaction times (TRT) in both the knee extensors and the plantar flexors. A resistance of 15% MVC applied during the RT task resulted in a lengthening of the motor time (MT) component in both groups prior to exercise. However, while knee extensor resisted motor time was lengthened by the exercise task, no such lengthening occurred in plantar flexor resisted RT. It is concluded that power-trained and endurance-trained athletes exhibit differences in response to a fractionated RT task, under both baseline and fatiguing exercise conditions.     

Fractioned reaction time in power-trained and endurance-trained athletes under conditions of fatiguing isometric exercise

Fractionated knee extensor and plantar flexor reaction time (RT) components were assessed in a group of eight weightlifters and eight long distance runners. Following a 4-day period of baseline stabilization for each muscle group, a 50% maximal voluntary contraction (MVC) holding-time exercise was administered. Results showed that the runners had longer premotor times (PMT) than the weightlifters in the knee extensors, but had much faster PMTs than the lifters in the plantar flexor condition. Compared to previously reported investigations using non-athletes, the data for the present sample of athletes indicated faster total reaction times(TRT) in both the knee extensors and the plantar flexors. A resistance of 15% MVC applied during the RT task resulted in a lengthening of the motor time (MT) component in both groups prior to exercise. However, while knee extensor resisted motor time was lengthened by the exercise task, no such lengthening occurred in plantar flexor resisted RT. It is concluded that power-trained and endurance-trained athletes exhibit difference in response to a fractionated RT task, under both baseline and fatiguing exercise conditions.     

Impulse Characteristics in Rapid Movement

Three untested assumptions of the impulse-variability model were examined in two experiments utilizing rapid, uni-planar limb movements. Experiment 1 varied movement distance (A) and movement time (MT) in a rapid-timing paradigm where the subject moved a lever through a certain distance in a certain time. Experiment 2 varied A in a reversal response where the S made a rapid elbow flexion and extension in a given MT. Displacement recordings were made on every trial. KR (knowledge of results) about MT was given after every trial. The results can be summarized as follows: (a) As predicted by the model, variations in impulse size and velocity were directly related to the impulses size; (b) There was no correlation between the accelerative and decelerative impulse durations recorded during the reversal response supporting the notion that the impulses might be independent; (c) Negative correlations (–.20 to –.50) were demonstrated between peak acceleration and impulse duration for both experiments, counter to the predictions of the model; and (d) Counter to the predictions of the model, timing error (VEt) increased as A decreased for rapid-timing responses. When the correlational results are taken into account, the model has the capacity to account for curvilinear relationships between relative timing error and movement speed. Overall, the results suggest that the impulse variability model requires some restructuring before it can be considered a viable model for the control of rapid limb movements.     

Decision time and movement time in depression: differential effects of practice before and after clinical improvement

Choice reaction time involves, at least two components of response latency, decision time and movement time. Studies of choice reaction time usually provide values of these two components averaged over a given number of trials. The aim of the present study of depressed subjects was to investigate changes across practice on Decision Time (DT) and Movement Time (MT) before and after clinical improvement. 19 depressed subjects were given two sessions of 50 trials each, one before treatment (Di) and one after recovery (Df). Decision time and movement time exhibited quite different patterns. Decision time significantly decreased with clinical improvement. No significant variation across trials was found, in either session. Movement time values varied across trials but the variations observed on Di and Df were significantly different, whereas before treatment latencies recorded at the end of the session were greater than those scored at the start, the contrary was observed after clinical recovery. No significant difference was found between values of movement time scored at the start of the two sessions.     

Impulse characteristics in rapid movement: implications for impulse-variability models

Three untested assumptions of the impulse-variability model were examined in two experiments utilizing rapid, uni-planar limb movements. Experiment 1 varied movement distance (A) and movement time (MT) in a rapid-timing paradigm where the subject moved a lever through a certain distance in a certain time. Experiment 2 varied A in a reversal response where the S made a rapid elbow flexion and extension in a given MT. Displacement recordings were made on every trial. KR (knowledge of results) about MT was given after every trial. The results can be summarized as follows: (a) As predicted by the model, variations in impulse size and velocity were directly related to the impulses size; (b) There was no correlation between the accelerative and decelerative impulse durations recorded during the reversal response supporting the notion that the impulses might be independent; (c) Negative correlations (-.20 to -.50) were demonstrated between peak acceleration and impulse duration for both experiments, counter to the predictions of the model; and (d) Counter to the predictions of the model, timing error (VEt) increased as A decreased for rapid-timing responses. When the correlational results are taken into account, the model has the capacity to account for curvilinear relationships between relative timing error and movement speed. Overall, the results suggest that the impulse variability model requires some restructuring before it can be considered a viable model for the control of rapid limb movements.     

Activity of wrist muscles elicited during imposed or voluntary movements about the elbow joint

To examine the coordination of muscles during multijoint movement, we compared the response of wrist muscles to perturbations about the elbow joint with their activation during a volitional elbow movement. The purpose was to test the following two predictions: (a) Responses can occur in muscles not stretched by the perturbation, as has been reported for other multijoint systems; and (b) the motor pattern in response to a perturbation mimics an opposing volitional motor pattern across the two joints. We recorded the electromyographic (EMG) activity of elbow and wrist muscles as well as the flexion/extension motions at the elbow and wrist joints during individual trials that either involved a response to a torque perturbation that extended the elbow or required volitional elbow flexion. The results of this study confirmed that responses were elicited in the nonstretched wrist muscles when the elbow joint was perturbed. The same motor sequence of elbow and wrist flexors was present for both the volitional and perturbation task (with the forearm supinated), regardless of whether the wrist joint was immobilized or freely moving. The findings suggest that the nervous system relies on the purposeful coupling of elbow and wrist flexors to counter the inertial effects during the unrestricted voluntary movement, even though the coupling does not appear to be purposeful during the perturbation or with the wrist immobilized. The coupling of elbow and wrist flexors, however, was not rigidly fixed, as evidenced by muscle onsets that adapted over repeated perturbation trials and a reversal of the wrist muscle activated (wrist extensor) when the forearm was pronated. Hence, the coupling of muscle activities can be modified quantitatively when not beneficial and can be altered qualitatively with different initial configurations of the arm.     

A novel clinical test of recognition reaction time in healthy adults

We evaluated a clinical "go/no-go" reaction time test (recognition RTclin) that is portable and does not require a computer, and used it to quantify the effect of age on recognition RTclin test scores. Fifty-two healthy adults 19-83 years old completed simple and recognition RTclin testing. Simple RTclin was measured as the elapsed time from initial release of a suspended vertical shaft by the examiner until its arrest by participant pinch grip. Recognition RTclin was similar except that a light on the apparatus randomly illuminated in 50% of the trials to signal the participant to arrest the device. To help interpret the RTclin results, we partitioned them into premovement time (PMT) and movement time (MT) using an optoelectronic camera system that is not ordinarily part of the RTclin test. Recognition RTclin scores were significantly slower than simple RTclin scores, with 71% of the prolongation attributable to PMT. While simple RTclin test scores correlated with age, recognition RTclin scores did not. A strong negative association between recognition RTclin accuracy and age was found. Recognition RTclin is feasible to measure in healthy adults and appears to represent a portable, computer-independent measure of cognitive processing speed and inhibitory capacity. Potential applications include assessment of brain injury, dementing illness, medication side effects, fall risk, and safe driving.     

Does functional performance and upper body strength predict upper extremity reaction and movement time in older women?

BackgroundReaction time to initiate upper limb movement and movement time to place hands on the landing surface may be important factors in forward fall landing and impact, contributing to injury reduction. The aim was to investigate the relationship of physical function and upper body strength to upper limb reaction and movement time in older female participants.Methods75 female participants (72 ± 8 yrs) performed 5 arm response trials. Reaction time (signal to initiation of movement), and movement time (initial movement to contact), were collected using 3D motion capture. Additional variables were: handgrip; sit-to-stand; shoulder flexion and elbow extension strength measured by hand-held dynamometry; one-legged balance; fall risk; and physical activity scores. Prediction variables for reaction and movement time were determined in separate backward selection multiple regression analyses. Significance was set at P < 0.05.FindingsSignificant regression equations for RT (r² = 0.08, P = 0.013) found a relationship between stronger handgrip (Beta = −0.002) and faster reaction time, accounting for 8% variance. For movement time (r² = 0.06, P = 0.036) greater shoulder flexion strength (Beta = −0.04) was related to faster movement time, explaining 6% variance. Stronger SF strength was related to a decrease in MT by 4%.DiscussionA relationship between arm strength measures and faster upper body reaction and movement time was shown, with 10–20% higher strength associated with a 5% faster response time. Even though this was a relatively weak relationship, given that strength is a modifiable component this provides a potential avenue for future intervention efforts. This in turn could have an impact on forward fall landing and potential reduction of injury risk.     

Reaction time,movement time,and intelligence

Speed of information processing is measured in terms of reaction time (RT) and movement time (MT) to five stimulus displays which differ in the amount of information transmitted, over a range from 0 to 3 bits of information. RT, but not MT, increases as a linear function of the number of bits in the stimulus display. RT and MT show reliable individual differences which are significantly correlated with intelligence as measured by Raven's Standard Progressive Matrices.     

Performance on a reciprocal tapping task with variations in intertapping interval

Fitts' law was investigated in a study of the effect of the index of difficulty (ID) and intertapping interval upon reaction time (RT) and movement time (MT) for a reciprocal tapping task. ID showed its well-established relationship with MT as described by Fitts' law: MT = aID + b. Improvement in the linearity of this relationship was, however, demonstrated by expressing MT in logarithmic units. While ID had an unsubstantial (though significant) effect on RT, increases in intertapping interval from zero to any level of discrete tapping led to significant increases in RT of about 135 msec. The results are interpreted as lending support to Fitts' thesis that RT and MT reflect independent phases of information processing.     

Choice reaction time of elbow flexion and extension during passive elbow motions

The effect of passive elbow motions on electromyographic reaction times (EMG-RTs) of the biceps brachii for elbow flexion and the triceps for elbow extension was investigated in 8 normal subjects, using a choice-RT task, in which the subject was uncertain about the response direction to perform until the arrival of response signal after the passive motion started. Compared to the static condition, choice EMG-RTs shortened only when the direction of passive and response movements was the same. It seems that passive motions act as prior information on direction of movement in the choice-RT task.     

Response strategies and the Simon effect

The study investigated whether the Simon effect, and its facilitation and interference components, shows up in reaction time (RT) or in movement time (MT), depending on the response strategy. Experiment 1 replicated a study by Hietanen and Rämä. Subjects had to press one of two lateralised keys in response to one of two stimuli. The stimuli were presented in the center (neutral condition) or to the left or right side (corresponding or non-corresponding conditions). To press the response key, a reaching movement was necessary, and both RT and MT were recorded. One group of subjects showed an RT facilitation effect and an MT interference effect. Another group of subjects showed both MT facilitation and MT interference effects. It was hypothesized that the two groups used different response strategies. In Exps. 2 and 3, the subjects were explicitly instructed to use the two strategies that were hypothesized for Exp. 1. The results showed that whether facilitation and interference manifest themselves in RT or MT depends on the response strategy adopted by the subjects.     

Effects of time uncertainty and instructed muscle tension on fractionated reaction time

Abstract: An experiment was conducted to examine the effects of time uncertainty and instructed muscle tension on the reaction time of elbow flexion. Twenty-two right-handed subjects were asked to respond to an audio stimulus by flexing their right elbow under four conditions (2 time uncertainty × 2 instructed muscle tension). Electromyograms (EMGs) were recorded from the biceps and triceps on the subject's right side. Reaction time was divided into premotor time and motor time, based on the difference between the EMG and elbow flexion response. Analysis of reaction time showed that the effects of time uncertainty and instructed muscle tension were additive. Time uncertainty affected premotor time only, and instructed muscle tension affected motor time only. These results are discussed in terms of the assumption that premotor time is a reflection of the central nervous system and motor time is a reflection to the peripheral muscle system.     

The effect of training and handedness on the performance of two simple motor tasks

In the first experimental series nine right-handed and nine left-handed subjects were tested on each side on two tasks. The first task measured the accuracy of reproduction of pressure in attempted extension of the elbow joint, and the second the speed of oscillation of attempted flexion and extension of the elbow joint. The results showed no significant difference in performance on the two sides in the accuracy task but a significant difference in performance on the speed task.

In the second experimental series the effect of 15-minutes daily training on each of two tasks over a four-week period was investigated on six subjects. The two tasks were the same as those used in the first experimental series, and attempted movement at the metacarpo-phalangeal joint as well as the elbow joint was studied. The mean results of all subjects showed a significant reduction in the mean error of the “accuracy” task over the training period for both the finger and arm. However, further analysis suggests that this may have been due to a clarifying of the subjects' concept of the target value rather than an improvement in his ability to grade the appropriate muscle contractions. A significant increase in the mean speed of oscillation over the training period was also recorded for both finger and arm. This improvement was accompanied in most instances by a corresponding decrease in variation of cycle length of the individual oscillations, which is interpreted as an improvement in the subjects' “timing” of the appropriate muscle contractions.     

Temporal characteristics of a comparator in adaptation to optical tilt

Two groups of eight Ss each and one group of seven Ss were exposed to optical tilts (T) of 50, 40, 30, 20, and 10 deg in succession. Exposure time at each tilt was 3, 15, and 27 min in Groups 1, 2, and 3, respectively. Trend analyses of the functions relating level of adaptation to T showed significant quadratic components for Group 1, quadratic and linear components for Group 2, and only linear components for Group 3. These results were consistent with derivations from a memory-comparator model of perceptual adaptation.     

Selective effects of barbiturate and amphetamine on information processing and response execution

In a 3 × 2 × 2 factoral experiment, 12 subjects carried out a choice reaction task with reaction time (RT) and movement time (MT) as response measures.Independent variables were drug treatment (amphetamine, barbiturate, placebo), visual stimulus degradation and S-R compatibility. Visual stimulus degradation and S-R compatibility showed additive effect on the RT, but did not affect the MT. This confirms that stimulus encoding, response selection and response execution represent independent processing stages. The two drugs had selective effects on the RT and the MT. Barbiturate (as compared to placebo) had no effect on the MT, but it lengthened the RT, and this effect was additive with the effects of S-R compatibility but showed an interaction with the effects of stimulus degradation. Amphetamine (as compared to placebo) shortened the MT, but there was no significant main effect of amphetamine on the RT although the interaction with the effect of S— compatibility was significant. These results suggest that barbiturate affects stimulus encoding whereas amphetamine affects response-related processes..