Motor Strategies in Lifting Movements

The experiment compares the performances of children six to nine years old and adults in a simple, monoarticular lifting task. Overt behaviors, as described by the kinematic features of the movement, do not differ qualitatively in the two groups. The patterns of motor commands, as expressed by the electromyographic recordings, are however strikingly different. Adults plan the movement with a careful balance between agonist muscle activity and passive, viscoelastic forces, whereas children use both agonist and antagonist active forces. It is argued that the motor strategy adopted by adults depends upon an internal representation of the properties of the motor system and of the size/weight covariation in natural objects, and that this representation is not yet fully developed at nine years of age.     

Development of interactions between sensorimotor representations in school-aged children

Reliable sensory-motor integration is a pre-requisite for optimal movement control; the functionality of this integration changes during development. Previous research has shown that motor performance of school-age children is characterized by higher variability, particularly under conditions where vision is not available, and movement planning and control is largely based on kinesthetic input. The purpose of the current study was to determine the characteristics of how kinesthetic-motor internal representations interact with visuo-motor representations during development. To this end, we induced a visuo-motor adaptation in 59 children, ranging from 5 to 12 years of age, as well as in a group of adults, and measured initial directional error (IDE) and endpoint error (EPE) during a subsequent condition where visual feedback was not available, and participants had to rely on kinesthetic input. Our results show that older children (age range 9–12 years) de-adapted significantly more than younger children (age range 5–8 years) over the course of 36 trials in the absence of vision, suggesting that the kinesthetic-motor internal representation in the older children was utilized more efficiently to guide hand movements, and was comparable to the performance of the adults.     

The Post-Movement Beta Rebound and Motor-Related Mu Suppression in Children

Abstract

Age-related EEG activity change is a prominent feature that reflects the functional development of the brain. The current study investigated the beta and mu rhythms of 16 children (7.7 ± 1.5 years, 5 to 9.6 years) and 13 adults when a self-determining arm motion was performed. The results indicated that mu power was decreased during movement and returned to baseline level after the movement for both children and adults. However, although a decrease in beta power was observed for both children and adults during movement, the post-movement beta power rebound (PMBR) was observed in adults but not in children. These results suggest that motor-related mu suppression develops early in children; PMBR develops later and may be associated with a more prolonged motor development process.     

Movement segmentation and visual perturbation increase developmental differences in motor control and learning

We examined the developmental differences in motor control and learning of a two‐segment movement. One hundred and five participants (53 female) were divided into three age groups (7–8 years, 9–10 years and 19–27 years). They performed a two‐segment movement task in four conditions (full vision, fully disturbed vision, disturbed vision in the first movement segment and disturbed vision in the second movement segment). The results for movement accuracy and overall movement time show that children, especially younger children, are more susceptible to visual perturbations than adults. The adults’ movement time in one of the movement segments could be increased by disturbing the vision of the other movement segment. The children's movement time for the second movement segment increased when their vision of the first movement segment was disturbed. Disturbing the vision of the first movement segment decreased the percentage of central control of the second movement in younger children, but not in the other two age groups. The children's normalized jerk was more easily increased by visual perturbations. The children showed greater improvement after practice in the conditions of partial vision disturbance. As the participants’ age increased, practice tended to improve their feedforward motor control rather than their feedback motor control. These results suggest that children's central movement control improves with age and practice. We discuss the theoretical implications and practical significance of the differential effects of visual perturbation and movement segmentation upon motor control and learning from a developmental viewpoint.     

A developmental study of the influence of task characteristics on motor overflow

Motor overflow refers to involuntary movement or muscle activity that may coincide with voluntary movement. This study examined factors influencing motor overflow in 17 children (8-11 years), and 17 adults (18-35 years). Participants performed a finger pressing task by exerting either 33% or 66% of their maximal force output using their dominant or non-dominant hand. Attention was manipulated by tactile stimulation to one or both hands. Overflow relative to the target force was greater in children compared to adults, and at the lower target force for both groups, but was not influenced by attentional stimulation. Childhood overflow was greater when the left-hand performed the task. Although an immature motor system may underlie an inability to suppress involuntary movement, childhood overflow may provide motor stabilization.     

The role of segmental mass and moment of inertia in dynamic-contact task construction

The authors examined whether differences between children and adults in the application of muscle forces during a dynamic-contact task (cycling) can be attributed to children's relatively lower segmental mass and moment of inertia. They examined pedal-force construction as adults and younger and older children (n = 7 in each group), with and without mass added to their limbs, pedaled an appropriately scaled bicycle ergometer. When mass was added to their limbs, children adjusted muscular forces on the pedal in a way that began to approach the pattern demonstrated by adults. Because age, neuromotor maturation, and motor experience were held constant, it seems plausible that by 6 to 8 years of age, and perhaps younger, physical size and growth limit children's production of adult-like muscle forces on the pedal.     

Individual differences in motor development during early childhood: An MEG study

In a previous study, we reported the first measurements of pre‐movement and sensorimotor cortex activity in preschool age children (ages 3–5 years) using a customized pediatric magnetoencephalographic system. Movement‐related activity in the sensorimotor cortex differed from that typically observed in adults, suggesting that maturation of cortical motor networks was still incomplete by late preschool age. Here we compare these earlier results to a group of school age children (ages 6–8 years) including seven children from the original study measured again two years later, and a group of adults (mean age 31.1 years) performing the same task. Differences in movement‐related brain activity were observed both longitudinally within children in which repeated measurements were made, and cross‐sectionally between preschool age children, school age children, and adults. Movement‐related mu (8–12 Hz) and beta (15–30 Hz) oscillations demonstrated linear increases in amplitude and mean frequency with age. In contrast, movement‐evoked gamma synchronization demonstrated a step‐like transition from low (30–50 Hz) to high (70–90 Hz) narrow‐band oscillations, and this occurred at different ages in different children. Notably, pre‐movement activity (‘readiness fields’) observed in adults was absent in even the oldest children. These are the first direct observations of brain activity accompanying motor responses throughout early childhood, confirming that maturation of this activity is still incomplete by mid‐childhood. In addition, individual children demonstrated markedly different developmental trajectories in movement‐related brain activity, suggesting that individual differences need to be taken into account when studying motor development across age groups.     

Tracking with and without target in 6- to 15-year-old boys

It is well documented that, in adults, manual tracking of a visual periodic target is very accurate in a wide variety of experimental conditions. With children between 5 and 9 years of age, however, the response lags significantly behind the stimulus. The first study presented here attempts to described the acquisition of this skill by children between 9 and 15 years of age. Within this age span, adult proficiency in pursuing a rapid target was approached through an improvement in response synchronization. Yet adults were distinguishable from the oldest children by a fundamentally different mode of movement execution: The former maintained a smooth modulation of the proper motor pattern, whereas the latter relied mainly on corrections through visual feedback. The second experiment showed that these different perceptuomotor strategies may be related to the availability of a more accurate and stable motor pattern with age. Young children had difficulties reproducing the stimulus after it was withdrawn, with performance deteriorating as the trial progressed. The initial mismatch and the following drift tended to decrease with age, even though the oldest children's stationary performance was still not as consistent with the target motion as the adult response.     

A Linked Muscular Activation Model for Movement Generation and Control

A new model for movement control is presented which incorporates characteristics of impulse-variability and mass-spring models. Movements in the model were controlled with phasic torque impulses in agonist and antagonist muscles and a tonic agonist torque.

Characteristics of the phasic agonist and antagonist torque profiles were based on observed properties of movement-related EMGs and muscle isometric torques. Variability of the phasic impulses depended on impulse magnitude as in impulse-variability models. The model therefore predicted a speed-accuracy tradeoff for limb movement. The time of onset and magnitude of the antagonist torque depended on the magnitude of the preceding agonist torque as indicated in studies of movement-related EMGs. This led to the new concept of linkage between the agonist and antagonist muscle forces which was shown to be important for reducing variability of fast movements. Progressive development of linkage during practice could explain the previous findings of decreased movement variability with practice coupled with increased variability of movement-related EMGs.

It was concluded that an inherently variable motor system deals with the variability associated with generation of large muscle forces by linking the forces produced by opposing muscles. In this way, variability in net joint torques and in movements can be decreased without the need for the nervous system to closely regulate the individual torques.     

Cognitive processing and motor execution in the lexical decision task: a developmental study

We investigated lexical decision making in children and adults by analyzing spatiotemporal characteristics of responses involving a hand movement. Children’s and adults’ movement trajectories were assessed in three tasks: a lexical decision task (LDT), a pointing task that involved minimal cognitive processing, and a symbol task requiring a simple binary decision. Cognitive interference on motor performance was quantified by analyzing movement characteristics in the LDT and symbol task relative to the pointing task. Across age groups, movements in the LDT were less smooth, slower, and more strongly curved to the opposite response option, and these interference effects decreased steadily with age. Older children showed stronger interference effects than did adults, even though their reaction times were similar to adults’ performance. No comparable effects were found in the symbol task, indicating that task characteristics such as response mapping and decision selection alone are not able to explain the developmental differences observed in the LDT. Our results indicate substantial overlap between cognitive processing and motor execution in the LDT in children that is not captured by computational models of visual word recognition and cognitive development.     

Stop using time reproduction tasks in a comparative perspective without further analyses of the role of the motor response: The example of children

The temporal reproduction task is often used to investigate inter-individual differences in the ability to perceive time without any further analyses of the contribution of motor responses to temporal performance. The present study examined the role of motor responses in the reproduction of a 2.5 s and a 4.5 s signal duration in children and adults, with the former producing longer motor responses. The results showed that the 2.5 s duration was overestimated, especially by the younger children, whereas the 4.5 s duration was underestimated in all age groups. Further analyses indicated that the developmental differences related to motor response time explained the age-related difference in temporal reproduction for the shorter duration but not for the longer duration. The modelling of our data suggests that, for the shorter signal duration, the children initiated their responses at the same time as the adults, but that they reproduced longer durations because their motor response took more time to complete. In contrast, for the 4.5 s duration, the children initiated their responses earlier than the adults. However, they reproduced duration values close to the target time because their motor responses took longer. In addition, whatever the duration value to be reproduced, the representation of the sample duration was more variable in the younger children.     

A linked muscular activation model for movement generation and control

A new model for movement control is presented which incorporates characteristics of impulse-variability and mass-spring models. Movements in the model were controlled with phasic torque impulses in agonist and antagonist muscles and a tonic agonist torque. Characteristics of the phasic agonist and antagonist torque profiles were based on observed properties of movement-related EMGs and muscle isometric torques. Variability of the phasic impulses depended on impulse magnitude as in impulse-variability models. The model therefore predicted a speed-accuracy tradeoff for limb movement. The time of onset and magnitude of the antagonist torque depended on the magnitude of the preceding agonist torque as indicated in studies of movement-related EMGs. This led to the new concept of linkage between the agonist and antagonist muscle forces which was shown to be important for reducing variability of fast movements. Progressive development of linkage during practice could explain the previous findings of decreased movement variability with practice coupled with increased variability of movement-related EMGs. It was concluded that an inherently variable motor system deals with the variability associated with generation of large muscle forces by linking the forces produced by opposing muscles. In this way, variability in net joint torques and in movements can be decreased without the need for the nervous system to closely regulate the individual torques.     

Imitation of body postures and hand movements in children with specific language impairment

Within the domain-general theory of language impairment, this study examined body posture and hand movement imitation in children with specific language impairment (SLI) and in their age-matched peers. Participants included 40 children with SLI (5 years 3 months to 6 years 10 months of age) and 40 children with typical language development (5 years 3 months to 6 years 7 months of age). Five tests were used to examine imitation and its underlying cognitive and motor skills such as kinesthesia, working memory, and gross motor coordination. It was hypothesized that children with SLI show a weakness in imitation of body postures and that this deficit is not equally influenced by the underlying cognitive and motor skills. There was a group effect in each cognitive and motor task, but only gross motor coordination proved to be a strong predictor of imitation in children with SLI. In contrast, hand movement imitation was strongly predicted by performance in the Kinesthesia task in typically developing children. Thus, the findings show not only that children with SLI performed more poorly on the imitation tasks than their typically developing peers but also that the groups’ performances showed qualitative differences. The results of the current study provide additional support to the view that the weaknesses in children with SLI are not limited to the verbal domain.     

Effects of Target Presentation Time,Recall Delay,and Aging on the Accuracy of Manual Pointing to Remembered Targets

The issues addressed in 2 experiments in which 10 younger and 10 older adults participated were (a) whether the retention of a target location in memory for motor control purposes would be facilitated by an increase in target presentation time; (b) whether increasing the recall delay since the last exposure to the target would have deleterious effects on aiming accuracy or variability, or both; and (c) whether those effects would be mediated by aging. The results revealed that there is a short-lived (< 1 s) visual representation of target location. In addition, the results suggested that the nature of that representation dictates a movement strategy favoring higher peak movement velocity. None of the effects reported in the present study was affected by age, suggesting that the coding and retrieving processes of target location in memory for motor control purposes are not affected by age.     

Effects of target presentation time, recall delay, and aging on the accuracy of manual pointing to remembered targets

The issues addressed in 2 experiments in which 10 younger and 10 older adults participated were (a) whether the retention of a target location in memory for motor control purposes would be facilitated by an increase in target presentation time; (b) whether increasing the recall delay since the last exposure to the target would have deleterious effects on aiming accuracy or variability, or both; and (c) whether those effects would be mediated by aging. The results revealed that there is a short-lived (< 1 s) visual representation of target location. In addition, the results suggested that the nature of that representation dictates a movement strategy favoring higher peak movement velocity. None of the effects reported in the present study was affected by age, suggesting that the coding and retrieving processes of target location in memory for motor control purposes are not affected by age.     

The spatial representation of power in children

Previous evidence demonstrates that power is mentally represented as vertical space by adults. However, little is known about how power is mentally represented in children. The current research examines such representations. The influence of vertical information (motor cues) was tested in both an explicit power evaluation task (judge whether labels refer to powerless or powerful groups) and an incidental task (judge whether labels refer to people or animals). The results showed that when power was explicitly evaluated, vertical motor responses interfered with responding in children and adults, i.e., they responded to words representing powerful groups faster with the up than the down cursor key (and vice versa for powerless groups). However, this interference effect disappeared in the incidental task in children. The findings suggest that children have developed a spatial representation of power before they have been taught power–space associations formally, but that they do not judge power spontaneously.     

Form and variability during sit-to-stand transitions: children versus adults

In performing the sit-to-stand transition, young children (6- to 7-year-olds) were expected to display a movement form similar to that of adults. However, movement consistency was predicted to be poorer in children than in adults because they lack refinement of motor control processes. Kinematic analysis of 10 repetitions of the sit-to-stand movement was carried out for 6 typically developing children and 6 adults. Supporting the authors' prediction of comparable form, no differences were evident between age groups for sequence of joint onsets, proportional duration of segmental motion, or in angle-angle plots of displacement at 2 segments. In contrast, within-participant variability was found to be higher for children: Coefficients of variation for most kinematic measures were twice those seen for adults. The authors interpret the children's lack of movement consistency as a reflection of inadequate stabilization of an internal model of intersegmental dynamics. Whereas adults have attained a skill level associated with refinement of that model, children have not. Children have an additional control problem because changes in body morphology throughout childhood require ongoing updating of the internal model that controls intrinsic dynamics.     

Form and Variability During Sit-to-Stand Transitions: Children Versus Adults

In performing the sit-to-stand transition, young children (6- to 7-year-olds) were expected to display a movement form similar to that of adults. However, movement consistency was predicted to be poorer in children than in adults because they lack refinement of motor control processes. Kinematic analysis of 10 repetitions of the sit-to-stand movement was carried out for 6 typically developing children and 6 adults. Supporting the authors' prediction of comparable form, no differences were evident between age groups for sequence of joint onsets, proportional duration of segmental motion, or in angle-angle plots of displacement at 2 segments. In contrast, within-participant variability was found to be higher for children: Coefficients of variation for most kinematic measures were twice those seen for adults. The authors interpret the children's lack of movement consistency as a reflection of inadequate stabilization of an internal model of intersegmental dynamics. Whereas adults have attained a skill level associated with refinement of that model, children have not. Children have an additional control problem because changes in body morphology throughout childhood require ongoing updating of the internal model that controls intrinsic dynamics.     

Influences of grasp selection in typically developing children

When reaching towards an object, adults favour grasps which, following the intended action, end in a comfortable position even when this requires them to start in an uncomfortable position (the end-state-comfort effect). However, this strategy is not consistently used by children who instead seem to favour a minimal pre-contact rotation of the hand, even when this results in an uncomfortable end position. In terms of multiple movements, the strategies used for grip selection are unclear; adults may still grasp for end-state-comfort given their propensity to plan to the end of a movement; however, children who are less able to concatenate movement may tend to start-state-comfort movements. The current study considered grip selection in children ranging from 4 to 12 years and in a group of adults. Participants were asked to rotate a disc so that an arrow pointed towards a specific target(s), the number of sequences in a movement was increased from one to three. Planning for end-state-comfort was seen in all participants and a clear developmental trajectory was identified whereby the relative comfort of an end position could be directly predicted by age in months. Adults and 10–12-year-olds favoured an end-state-comfort strategy whereas the younger children gave equal weighting to end-state-comfort, start-state-comfort and no initial rotation strategies. All groups were able to end a movement comfortably when it was composed of three steps; however, the proportion of movements relying on an end-state-comfort strategy decreased as sequence length increase whereas the proportion of start-state-comfort and no initial rotation strategies increased. The current data support the concept that a mechanism for planning grasps may be based on motor experience.     

Development of Force Adaptation During Childhood

Humans learn to make reaching movements in novel dynamic environments by acquiring an internal motor model of their limb dynamics. Here, the authors investigated how 4- to 11-year-old children (N = 39) and adults (N = 7) adapted to changes in arm dynamics, and they examined whether those data support the view that the human brain acquires inverse dynamics models (IDM) during development. While external damping forces were applied, the children learned to perform goal-directed forearm flexion movements. After changes in damping, all children showed kinematic aftereffects indicative of a neural controller that still attempted to compensate the no longer existing damping force. With increasing age, the number of trials toward complete adaptation decreased. When damping was present, forearm paths were most perturbed and most variable in the youngest children but were improved in the older children. The findings indicate that the neural representations of limb dynamics are less precise in children and less stable in time than those of adults. Such controller instability might be a primary cause of the high kinematic variability observed in many motor tasks during childhood. Finally, the young children were not able to update those models at the same rate as the older children, who, in turn, adapted more slowly than adults. In conclusion, the ability to adapt to unknown forces is a developmental achievement. The present results are consistent with the view that the acquisition and modification of internal models of the limb dynamics form the basis of that adaptive process.