The coding of constrained and preselected movement distance: Same-limb versus switched-limb reproduction

Three experiments were conducted to investigate the codes subserving the retention of movement extent information. Each experiment compared preselected and constrained movements in two independent movement tasks: same-limb reproduction and switched-limb reproduction. When movement direction was the same for both criterion and reproduction movements (experiment 1), same-limb reproduction was more accurate than switched-limb performance. With movement direction altered, however, switched-limb reproduction was equal to same-limb reproduction (experiment 2). These results were confirmed in experiment 3 which manipulated both movement direction and reproduction limb in a within-subject design. Furthermore, while preselected reproduction was superior to constrained reproduction in all three experiments, the two groups were not differentially affected by either the movement task or direction variables. The overall findings were interpreted as providing support for a multiple-cue memorial representation of movement extent and the notion of coding flexibility.     

Evidence for an outflow theory of skill.

We argue that central monitoring of efferent signals (CME) is a necessary and perhaps sufficient condition for the most accurate reproduction of a linear movement. In a movement duplication task where the subject sets or is given a criterion movement which he then attempts to reproduce, we argue that voluntary criterion and reproduction movements may be based upon some ‘pre-set’ instruction whereas passive movement duplication must be based upon proprioceptive information. We show that subjects can perform a visual signal detection task during the voluntary criterion movement which does not affect accuracy of reproduction. The same task carried out during the passive criterion movement does affect reproduction. These findings suggest that pick-up of proprioceptive information is not involved in voluntary movement.     

Coding processes in preselected and constrained movements: effect of vision

Three experiments were conducted in which visual information was manipulated either at the endpoint or during preselected, subject defined and constrained, experimenter-defined movements. In Experiments 1 and 2 the subject's task was to reproduce the movement in the absence of vision. Augmenting the terminal location of the criterion movement with vision had no differential effect on reproduction in Experiment 1, although preselected movement accuracy was significantly superior to constrained. Providing vision throughout the criterion movement in Experiment 2 not only failed to improve the accuracy of constrained movements but decreased reproduction performance in preselected movements. In Experiment 3 procedures were adopted to control the allocation of the subjects' attention during the criterion movement. The subjects reproduced by vision alone, movement alone, or with both visual and movement information available. When subjects were informed of the modality of reproduction prior to criterion presentation, they were able to ignore concurrent input from vision and attend to movement information. In the absence of precues visual information was spontaneously attended. The data were interpreted as contrary to closed-loop assumptions that additional information necessarily enhances the strength of a motor memory representation. Rather, they can be accommodated in terms of Posner, Nissen and Klein's (1976) theoretical account of visual dominance and serve to illustrate the importance of selective attention effects in movement coding.     

Interference Between Location and Distance Information in Motor Short-Term Memory: The Respective Roles of Direct Kinesthetic Signals and Abstract Codes

Interference between location and distance information in motor short-term memory has been hypothesized on the basis of the systematic pattern of undershooting and overshooting in movement reproduction that occurs when the starting position for reproduction movements is shifted. To determine the possible contribution of limb-specific kinesthetic information to this systematic undershooting-overshooting pattern, we compared the reproduction of linear arm positioning movements performed under either same-limb or switched-limb conditions. Ten subjects were assigned to either a location or distance cue condition, and each subject completed a total of 40 trials, 20 under same-limb and 20 under switched-limb conditions. Each trial consisted of criterion and reproduction movements, separated by a 10-s retention interval. The starting position for the reproduction movement was shifted by 0, 2, or 4 cm in either direction from that of the criterion movement. The systematic undershooting-overshooting pattern, which occurs when either the movement location or distance is reproduced, arose under both the same-limb and switched-limb conditions, suggesting that the primary cause of the location-distance interference is not limb-specific kinesthetic information. Rather, more abstract information in the form of a conceptual memory code appears to be the probable cause of the location distance interference phenomenon.     

Memory for Constrained and Preselected Movement Location and Distance

These experiments assessed the interrelationship between location and distance cues in the coding of movements. In separate experiments subjects recalled either the terminal location or the distance of constrained (Experiment 1) or preselected (Experiment 2) movements following a 15-sec retention interval. Changes in direction amd amplitude of starting position were used to ascertain whether recall errors were related to these changes. The findings of both experiments indicated that location and distance were recalled with similar accuracy when the starting position was identical for the criterion and recall movement. However, analysis of constant errors when the recall starting position was varied in either direction clearly indicated neither terminal location nor distance are coded independently, and memory for movement is based on an interaction between these cues.     

Cognitive Strategies and Short-term Memory for Movement Distance and Location

A number of researchers (e.g. Kerr, 1978; Walsh, Russell, Imanaka, & James, 1979) have previously demonstrated interference between location and distance information in motor short-term memory. This interference manifests itself in a characteristic pattern of undershooting and overshooting, with reproduction movement location being drawn in the direction of criterion movement distance and, conversely, the distance of reproduction movements being influenced by the terminal location of the criterion movement. We investigated the effects of different cognitive strategies upon the appearance of this location-distance interference during the reproduction of movement location (Experiment 1) and distance (Experiments 2 and 3) in a linear arm positioning task. Experiment 1 compared performance in location reproduction between two strategy groups differing in the availability of explicit information about the change in starting position. The characteristic undershooting-overshooting interference pattern was observed for the group without the explicit information about the change in starting position but disappeared for the group in which explicit information about the change in starting position was provided. Experiment 2 examined the systematic undershooting-overshooting pattern in distance reproduction for a location strategy (involving some extrapolation of the start and end locations), a counting strategy, and a distance sense strategy (involving the use of visual imagery). The systematic response bias pattern disappeared when the subjects used a location strategy but was clearly observed for the subjects using the other two strategies. This finding was generally confirmed by Experiment 3, which showed a typical undershooting-overshooting pattern in distance reproduction for a counting/distance sense strategy but not for two location strategies (a general location and an explicit location strategy). The location strategies differed in the availability of explicit information about starting and end locations for both the criterion and reproduction movements. The results from these three experiments indicate that explicit information about the start andlor end locations prevents the usual interference between location and distance information from arising in movement reproduction. The notions of automatic and controlled processing and cerebral hemispheric specialization are discussed as potential explanations of these results and of the interference typically observed in motor short-term memory between distance and location information.     

Mutual Interactions Between Speech and Finger Movements

Speech output and finger movements were recorded as right-handed males repeated a syllable while making cyclical finger movements in three experimental conditions: (a) maintaining constant amplitude in both response systems; (b) alternating speech amplitude while attempting to maintain constant finger movement amplitude; and (c) alternating finger movement amplitude while attempting to maintain constant speech amplitude. Observations showed that output of the two response systems was coupled (one syllable was uttered with each finger movement) and entrained in amplitude (the amplitude pattern of the response that the subject attempted to keep constant followed that of the concurrently-active amplitude-modulated response).

These interactions were bidirectional and were present with both left-handed and right-handed finger movements. The interactions are more extensive and subtle than mere interference with one response system by the other, and apparently do not depend on anatomical overlap of the responding neural systems.     

Decay and interference effects in motor short-term memory

Trace decay and interference effects in motor short-term memory were investigated by contrasting the predictions of two recent models (Pepper and Herman 1970; Laabs 1973) in regard to these two variables. Laabs' prediction that forgetting in motor short-term memory is indexed by greater variability of reproduction was supported in that movement reproduction after a 20 sec retention interval, either filled or unfilled, produced greater variable error. Further, his model was again supported in that analysis of constant error over five movement extents indicated interference effects through formation of an adaptation level which caused short movements to be overshot and long movements to be undershot. Pepper and Herman's concept of spontaneous trace decay indexed by a negative shift in constant error was not supported as was their prediction that interpolated activity would alter the strength of the criterion trace through an assimilation process. Finally, some evidence was found supporting the view that a memory trace can be strengthened through proprioceptive feedback entering through an unattended channel.     

Attentional requirements for location and distance of movement: encoding and recognition

The purpose of this experiment was to study the early processing stages of encoding and recognition of slow movement in a short-term motor-memory paradigm. These stages were examined by determining whether Laabs' (1973) differential decay rates for location of movement and distance of movement could be replicated when the interfering activity was performed during the criterion and replication movements. 20 subjects performed a linear-positioning task in a 2 X 2 X 2 (count X movement type X retention interval) experimental design. 10 subjects in one condition counted backwards by 3s during the criterion and replication movements. There were no detrimental effects for location and distance-cue reproduction when attention was shared with counting backwards. Like Laabs' results, location of movement was maintained over the 15-sec. interval while distance of movement spontaneously changed. These results supported the notion that the early stages of encoding and recognition of cues for movement can occur unaffected by a secondary task.     

Mutual interactions between speech and finger movements

Speech output and finger movements were recorded as right-handed males repeated a syllable while making cyclical finger movements in three experimental conditions: (2) maintaining constant amplitude in both response systems; (b) alternating speech amplitude while attempting to maintain constant finger movement amplitude; and (c) alternating finger movement amplitude while attempting to maintain constant speech amplitude. Observations showed that output of the two response systems was coupled (one syllable was uttered with each finger movement) and entrained in amplitude (the amplitude pattern of the response that the subject attempted to keep constant followed that of the concurrently-active amplitude-modulated response). These interactions were bidirectional and were present with both left-handed and right-handed finger movements. The interactions are more extensive and subtle than mere interference wtih one response system by the other, and apparently do not depend on anatomical overlap of the responding neural systems.     

Preselection and response biasing in short-term motor memory

Two experiments were performed comparing preselected (subject defined) and constrained (experimenter defined) movements. In the first experiment, subjects made reproduction responses immediately or under unfilled and filled 15-sec retention intervals. Results indicated that recall of preselected movements was clearly superior until the interpolation of information processing activity. In addition, preselected movements demonstrated no forgetting over a 15-sec retention interval while constrained movements evidenced spontaneous memory lass, suggesting that preselected movements possess a stronger representation in memory. The second experiment examined this interpretation in a response biasing paradigm. Subjects made criterion responses under preselected or constrained conditions, while the interpolated movement was always in the constrained mode and ± 40 deg from the criterion. The subjects' task was to attend to both movements and recall each when instructed. While preselected recall was clearly superior' to constrained recall, response biasing was clearly evident in both. The failure to find differential biasing effects was discussed in terms of the relative trace strength hypothesis (Stelmach & Welsh, 1972).     

Spatial Error Detection and Assimilation Effects in Rapid Single and Bimanual Aiming Movements

In 2 experiments, spatial error detection capability and movement accuracy were investigated in both single and bimanual rapid aiming movements. In both experiments, right-handed college-age participants (N = 40 [Experiment 1]; N = 24 [Experiment 2]) used light, aluminum levers to make quick single and dual reversal movements in the sagittal plane in a time to reversal of 210 ms to either the same or different target locations involving identical (Experiment 1) or mirror-image (Experiment 2) movements. In Experiment 1, the shorter-distance limb overshot the target by 15-23&percent; when paired with a limb traveling at least 20 degrees farther, but no spatial assimilations were shown when movements differed by 20 degrees or less. In Experiment 2, the shorter-distance limb overshot 22-29&percent; when paired with a limb traveling 20 degrees farther, but spatial assimilations were not mitigated when both limbs moved to the same target position. Participants underestimated movement amplitude in all dual conditions but particularly when spatial assimilations were noted. Correlations between actual and estimated errors decreased from single to dual trials in both experiments. The findings suggest that spatial assimilations are caused by bimanual differences in movement amplitude, regardless of movement direction, and that individuals have greater difficulty identifying errors in simultaneous actions, especially when spatial assimilations are present, than identifying errors in single-limb actions.     

Speed-accuracy characteristics of saccadic eye movements

Speed-accuracy trade-off characteristic of horizontal saccadic eye movements were examined in this study. Unlike limb movements, saccadic eye movements are preprogrammed, unidimensional, and do not involve target impact. Hence, they provide an optimal test of the impulse variability account of the speed-accuracy trade-off in rapid movements. Subjects were required to alternately look at two target lights as fast and as accurately as possible for a period of 10 s. Target lights subtended angles of 5, 10, 15, and 20 degrees. By restricting target distances to less than 20 degrees of arc, the speed-accuracy relation was examined for single horizontal saccadic movements of the eye. movement of the dominant eye was tracked with an infra-red eye monitoring device. Fifty saccadic movements of the eye were recorded for each target distance and used to compute the average amplitude, duration, and velocity of eye movements, as well as, movement endpoint variability. An increase in both average velocity and movement endpoint variability with increasing movement amplitude was found. This, together with the unique features of the eye movement system, support the impulse variability account of the speed-accuracy trade-off in rapid movements.     

Characteristics of velocity profiles of speech movements

The control of individual speech gestures was investigated by examining laryngeal and tongue movements during vowel and consonant production. A number of linguistic manipulations known to alter the durational characteristics of speech (i.e., speech rate, lexical stress, and phonemic identity) were tested. In all cases a consistent pattern was observed in the kinematics of the laryngeal and tongue gestures. The ratio of maximum instantaneous velocity to movement amplitude, a kinematic index of mass-normalized stiffness, was found to increase systematically as movement duration decreased. Specifically, the ratio of maximum velocity to movement amplitude varied as a function of a parameter, C, times the reciprocal of movement duration. The conformity of the data to this relation indicates that durational change is accomplished by scalar adjustment of a base velocity form. These findings are consistent with the idea that kinematic change is produced by the specification of articulator stiffness.     

Speed-Accuracy Characteristics of Saccadic Eye Movements

Speed-accuracy trade-off characteristic of horizontal saccadic eye movements were examined in this study. Unlike limb movements, saccadic eye movements are preprogrammed, unidimensional, and do not involve target impact. Hence, they provide an optimal test of the impulse variability account of the speed-accuracy trade-off in rapid movements. Subjects were required to alternately look at two target lights as fast and as accurately as possible for a period of 10 s. Target lights subtended angles of 5,10,15, and 20°. By restricting target distances to less than 20° of arc, the speed-accuracy relation was examined for single horizontal saccadic movements of the eye. Movement of the dominant eye was tracked with an infra-red eye monitoring device. Fifty saccadic movements of the eye were recorded for each target distance and used to compute the average amplitude, duration, and velocity of eye movements, as well as, movement endpoint variability. An increase in both average velocity and movement endpoint variability with increasing movement amplitude was found. This, together with the unique features of the eye movement system, support the impulse variability account of the speed-accuracy trade-off in rapid movements.     

Memory for movement in blind children: the role of previous visual experience

The role of previous visual experience in the reproduction of a criterion movement was examined in sighted, late-blinded, and congenitally blind children. Results showed that the congenitally blind reproduce movements at a low level of accuracy compared with the other two groups. Detailed analysis showed that although the congenitally blind could reproduce the extent of the movement accurately, the movement was poorly reproduced in terms of its orientation to the criterion movement and its orientation from a reference point. The role of prior vision in establishing a frame of reference is discussed.     

Adaptation to visual displacement with active and passive limb movements: effect of movement frequency and predictability of movement

Three experiments were performed to evaluate the influence of active and passive limb movements on adaptation to visual displacement. Over a wide frequency range (0·5-1·25 Hz) with constant amplitude, 30°, significant adaptation was achieved with active and passive movements. When arm movement frequency was constant at 1·0 Hz but amplitude of movement was varied, less adaptation was achieved for both active and passive movements than when amplitude was held constant. Even at a frequency above that of most naturally occurring limb movements, 1·67 Hz, and with variable amplitude motion, significant adaptation was achieved with active and passive limb movements. These findings emphasize the importance of visual-proprioceptive discordances for adaptation to visual displacement when only sight of the hand is permitted. Significant differences did not appear between the active and passive movement conditions in any of the experiments.     

The Coding of Location

One prediction of the recent target hypothesis for movement control (MacNeilage, 1970; Russell, 1976) holds that location reproduction is not solely dependent upon stored kinesthetic information. Three experiments were performed to test this prediction by requiring the subject to reproduce the location with the limb opposite to the one used for criterion production. This switched-limb procedure was assumed to force the subject to rely upon more abstract information rather than the kinesthetic cues of the criterion movement. With movement direction invariant, switched-limb reproduction was equal to same-limb reproduction. The alteration of movement direction hampered switched-limb reproduction but same-limb reproduction was not greatly affected. These findings gave some support to the target hypothesis but suggested that the context of the movement may affect the potency of the location code. Implications of the switched-limb technique for future research were briefly discussed.     

Visual dominance in a lateral plane motor learning task.

Visual dominance was investigated in a motor learning task with the criterion movement being in the lateral plane of the body. The criterion movement was a 10-in. abduction of the arm. All subjects received four presentation trials for the criterion movement in each of the following conditions: dominant rotated arm, dominant unrotated arm, nondominant rotated arm, and nondominant unrotated arm. Three independent groups of 10 college-age subjects differed according to sensory stimuli given during presentation trials. The Kinesthetic group was blindfolded for presentation trials. The Visual and Kinesthetic group was unblindfolded for presentation trials. The Alternating group was blindfolded on half of the presentation trials and unblindfolded on the other half. All subjects carried out five blindfolded reproduction trials for each of the four conditions. Absolute error for the length of the reproduced movements was measured and no significant difference between groups was found. This suggests that visual dominance is reduced in movements outside the frontal plane when focal vision is not used. Planned comparison testing indicated the Alternating group was significantly more accurate than the Visual and Kinesthetic group.     

Retention characteristics of movement rate information

The retention characteristics of fast and slow movements were investigated in two experiments. Experiment 1 examined the reproduction of either fast or slow preselected movement rates after 0-sec rest, 15-sec rest or a 15-sec filled delay. Both fast and slow movement rates were rehearsable. Experiment 2 examined reproduction accuracy after subjects were required to perform a competing secondary task during the production of fast and slow movements. Although the secondary task degraded the reproduction of slow movements, it had no apparent effect upon the reproduction of fast movements. These results were interpreted as indicating partial support for Jones' (1974) notion of central monitoring of efference, and suggested that the contribution of proprioceptive feedback to movement control varies as a function of movement rate.