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Biomedical subjects

Simon J Bennett

Publications and source records attributed to Simon J Bennett.

17 recordsLinked to original sources

Smooth ocular pursuit during the transient disappearance of an accelerating visual target: the role of reflexive and voluntary control.

This study examined the extent to which human subjects predict future target motion for the control of smooth ocular pursuit. Subjects were required to pursue an accelerating target (0, 4 or 8 degrees/s2) that underwent a transient occlusion, and consequently reappeared with the same or increased velocity. Presentations were received in a random or blocked order. Subjects exhibited anticipatory smooth pursuit prior to target motion onset, which in blocked presentations was scaled to the velocity generated by the target acceleration. In random presentations subjects also exhibited anticipatory smooth pursuit, but this was reflected in a more generalized response. During the transient occlusion all subjects exhibited a reduction in eye velocity, which was followed in the majority by a recovery prior to target reappearance. In random presentations, eye velocity decayed and recovered to a level that followed on from the response to the initial ramp. In blocked presentations, there was evidence of improved scaling throughout, which culminated in a significant increase in eye velocity between the start and end of the transient occlusion (8 degrees/s2 only). These findings are difficult to reconcile with reflexive accounts of oculomotor control that perpetuate current eye motion, and hence generate a simple form of prediction using a direct efference copy ("eye-velocity memory"). Rather, they are more consistent with the scaling of smooth pursuit eye movements by means of a more-persistent velocity-based representation, which plays a significant role in both random and blocked stimulus presentations.

Acceleration↗

Observational modeling effects for movement dynamics and movement outcome measures across differing task constraints: a meta-analysis.

The authors conducted a meta-analysis of the observational modeling literature to quantify overall between-participants treatment effects obtained when movement behaviors are acquired. Effects were obtained and reported separately for movement dynamics (MD) and movement outcome (MO) measures. The overall mean observational modeling treatment effects (delta(u)Bi) were 0.77 and 0.17, respectively, for MD and MO measures. The effects reflected a significant advantage of observational modeling over practice-only control conditions. Most important, the magnitude of the obtained effects was far stronger for MD than for MO measures, confirming a distinctive response to observational modeling during motor learning. The advantage for MD measures over observational modeling measures was replicated for different types of tasks. Observational modeling was particularly beneficial for serial tasks (delta(u)Bi = 1.62 and 0.61, respectively, for MD and MO). There were slightly reduced effects for continuous tasks (delta(u)Bi = 1.01 and 0.51, respectively, for MD and MO) and smaller to medium-sized effects for discrete tasks (delta(u)Bi = 0.56 and 0.10, respectively, for MD and MO). The authors discuss those findings with reference to the visual perception perspective on observational modeling, i.e., that demonstrations primarily convey relative motions required to approximate modeled movement behaviors.

Attention↗

Combined smooth and saccadic ocular pursuit during the transient occlusion of a moving visual object.

Accurate ocular pursuit during a transient occlusion interval would minimize retinal position and velocity error, and could provide an advantage when discriminating object characteristics at reappearance. This study was designed to examine how the smooth and saccadic response extrapolates the trajectory of a moving visual object during a transient occlusion. We confirmed that subjects could not maintain unity gain smooth pursuit during the transient occlusion. Eye velocity decayed significantly without visual feedback but then in the majority of subjects, there was a recovery that brought eye velocity back towards object velocity. However, eye velocity did not increase to a level that eliminated the developing position error. Subjects corrected for the resulting error in eye position by releasing saccades that generally placed the eye ahead of the occluded object's extrapolated position. The majority of saccadic correction occurred between 220 and 600 ms of the occlusion interval, and when combined with the smooth response enabled accurate pursuit of a 10 degrees/s object for up to 1,200 ms of occlusion. The lack of saccadic correction after 600 ms of occlusion combined with the reduced eye velocity resulted in significant undershoot of eye position at the moment of object reappearance when pursuing an 18 degrees/s object. We suggest that extra-retinal information regarding eye velocity and smooth eye displacement could be available from a continually updating efference copy of eye motion in MST, whereas a veridical representation of extrapolated object velocity and displacement could be obtained from persistent activity in FEF.

Adult↗

Evidence for synergy between saccades and smooth pursuit during transient target disappearance.

Visual tracking of moving objects requires prediction to compensate for visual delays and minimize mismatches between eye and target position and velocity. In everyday life, objects often disappear behind an occluder, and prediction is required to align eye and target at reappearance. Earlier studies investigating eye motion during target blanking showed that eye velocity first decayed after disappearance but was sustained or often recovered in a predictive way. Furthermore, saccades were directed toward the unseen target trajectory and therefore appeared to correct for position errors resulting from eye velocity decay. To investigate the synergy between smooth and saccadic eye movements, this study used a target blanking paradigm where both position and velocity of the target at reappearance could vary independently but were presented repeatedly to facilitate prediction. We found that eye velocity at target reappearance was only influenced by expected target velocity, whereas saccades responded to the expected change of target position at reappearance. Moreover, subjects exhibited on-line adaptation, on a trial-by-trial basis, between smooth and saccadic components; i.e., saccades compensated for variability of smooth eye displacement during the blanking period such that gaze at target reappearance was independent of the level of smooth eye displacement. We suggest these results indicate that information arising from efference copies of saccadic and smooth pursuit systems are combined with the goal of adjusting eye position at target reappearance. Based on prior experimental evidence, we hypothesize that this spatial remapping is carried out through interactions between a number of identified neurophysiological structures.

Adaptation, Physiological↗

Timing the anticipatory recovery in smooth ocular pursuit during the transient disappearance of a visual target.

After the disappearance of a moving target and the loss of visual feedback regarding image motion, smooth pursuit eye velocity decays rapidly. If, however, there is an expectation the target will reappear further along its trajectory, there is a scaled recovery in eye velocity before target reappearance. The aim of this study was to examine whether the timing of the anticipatory recovery is influenced by the duration of transient target disappearance. We found that subjects (N=6) did not maintain eye velocity close to target velocity throughout the inter-stimulus interval (ISI). In general, after an initial reduction in eye velocity a significant increase was observed for most subjects before target reappearance, or a recovery that halted the decay. The timing of the recovery was not influenced by ISI even when this was predictable. There was, however, a significant effect of the initial visible ramp duration, indicating that the recovery was a consequence of the previous eye velocity trajectory and subsequent reacceleration. We suggest, therefore, that the recovery was timed to the moment of target disappearance rather than reappearance, and was the result of reactivation of a variable gain mechanism that acts on the visuomotor drive to ocular pursuit.

Brain↗

Perceptual-motor organization of children's catching behaviour under different postural constraints.

The experiment investigates the perceptual-motor organization underlying children's catching performance when the demands on the postural system are varied. For this purpose, one-handed catching performance was observed under different postural constraints in children aged 9-10 years. Two groups of eleven participants, classified as either good or poor catchers, performed one-handed catches under three different postural conditions: standing, sitting, and standing while pressing a button positioned to a postural support aid (PSA). Results revealed, first, that when seated, poor catchers approached the level of the good catchers' performance. Second, poor catchers improved their performance by using the PSA, but not to the same performance as when sitting. Third, there was no effect of postural condition on the performance of the good catchers. The performance increase in the poor catchers is attributable to a combined change in functional postural sway and better timed movement of the catching hand, made possible by exploiting the extra surface support area afforded by sitting.

Biomechanical Phenomena↗

Coordination of reaching in children with spastic hemiparetic cerebral palsy under different task demands.

Coordination of reaching with the impaired and non-impaired arm in 10 children with spastic hemiparetic cerebral palsy (SHCP) was examined in a stationary ball and moving ball context. Kinematic data on trunk, arm, and wrist movements, and coordination patterns between joint angles of elbow, shoulder, and trunk, were analyzed to determine how reaching was influenced by impairment and object motion. Results showed longer deceleration time and movement time and greater trunk contribution following decreased elbow and shoulder excursion when reaching with the impaired arm compared to the non-impaired arm. The coordination of joint angle pairs showed little linearity for the impaired arm, indicating more segmented movements of shoulder and elbow. It was also found that coordination patterns between elbow, shoulder, and trunk displayed less similarity when reaching with the impaired arm compared to the non-impaired arm in both stationary and moving ball conditions. Regardless of the timing constraints, children with SHCP could make successful interceptions using the impaired arm, indicating that they coordinated and controlled the degrees of freedom within their own functional possibilities.

Arm↗

Postural stability and hand preference as constraints on one-handed catching performance in children.

Effects of postural state and hand preference as constraints on 1-handed catching performance were investigated in different ability groups of children aged 9-10 years. On the basis of pretest data, the authors classified 48 participants into groups of good, intermediate, and poor catchers (n = 16 in each) and asked them to perform 1-handed catches with their preferred and nonpreferred hands while standing and sitting. The good catchers' performance was not affected by the imposed postural constraints but did improve when they used the preferred hand. A similar effect of hand preference was evident in the intermediate and poor catchers, but there was also an effect of postural constraint. Independent of hand preference, intermediate catchers' performance while seated improved significantly compared with that during standing. For poor catchers, there was an interaction between hand preference and posture; significant improvement was evident only when they used the preferred hand in the sitting condition. The finding that manipulation of posture and hand preference affected performance outcomes indicates that perceptual skill is not the only influence on catching performance in children. Manipulation of those key constraints may facilitate the acquisition of catching skill, but more research is needed to determine the permanence of those effects.

Aptitude↗

Coordinating degrees of freedom during interceptive actions in children.

The aim of the experiment was to examine how children coordinate the degrees of freedom of the arm and trunk when performing interceptive actions that correspond to daily life activities. For that purpose, children were required to reach and grasp a stationary ball while standing (condition C1), a stationary ball while walking (C2), and a moving ball while standing (C3). The resulting movements were measured in world-centered and body-centered coordinates, and then subjected to three-dimensional kinematic analysis. The different coordinate frames of reference were used to determine the interaction between arm and trunk movements. Children adapted their coordination in the two moving conditions (C2 and C3) by decelerating longer towards the ball and exhibiting more interaction between the arm and trunk movements than in the stationary condition (C1). These results indicate that, like adult participants, children adapt to the constraints imposed by complex, interceptive actions by recruiting additional degrees of freedom of the trunk, which are coordinated with the hand to produce a movement that preserves an appropriate level of impact at hand/object collision.

Adaptation, Physiological↗

Predictive smooth ocular pursuit during the transient disappearance of a visual target.

When a moving target disappears and there is a complete absence of visual feedback signals, eye velocity decays rapidly but often recovers to previous levels if there is an expectation the target will reappear further along its trajectory Given that eye velocity cannot be maintained under such circumstances, the anticipatory recovery may function to minimize the developing velocity error. When there is a change in target velocity during a transient, any recovery should ideally be scaled and hence predictive of the expected target velocity at reappearance. This study confirmed that subjects did not maintain eye velocity close to target velocity for the duration of the inter-stimulus interval (ISI). The majority of subjects exhibited an initial reduction in eye velocity followed by a scaled recovery prior to target reappearance. Eye velocity during the ISI was, therefore, predictive of the expected change in target velocity. These behavioral data were simulated using a model in which gain applied to the visuomotor drive is reduced after the loss of visual feedback and then modulated depending on subject's expectation regarding the target's future trajectory.

Adult↗

The effects of intermittent vision on prehension under binocular and monocular viewing.

The aim of the present study was to examine the effects of intermittent binocular and monocular vision on the preparation and execution of the transport and grasp phases of prehension, and hence the temporal limit of binocular and monocular integration. Participants in two groups (speed or accuracy) performed prehensile movements of two amplitudes (20 and 40 cm) to either a large or small object (6 x 6 x 2 and 6 x 4x 2 cm) under conditions of binocular and monocular viewing. The interval between visual samples was manipulated with liquid crystal goggles (continuous vision, 20on/60off, and 20on/120off ms). A kinematic analysis indicated that participants modified variables associated with the preparation and execution of prehension in the intermittent vision conditions when instructed to emphasize accuracy. Participants instructed to emphasize speed, modified variables associated with the preparation phase only. The impact of intermittent vision was similar under binocular and monocular viewing. Thus, for prehension, it appears that consecutive binocular or monocular samples need to occur less than 60 ms apart in order to be fully integrated for limb control.

Adult↗

Human ocular pursuit during the transient disappearance of a visual target.

During the course of pursuing a moving target there are often periods of transient disappearance as it moves behind objects and surfaces. In experimental settings, eye velocity decays rapidly on the extinction of a moving target. However, eye velocity does not decay to zero if there is an expectation the target will reappear further along its trajectory. Increasing eye velocity to coincide with target reappearance could minimize the developing velocity error, but it remains to be empirically verified whether this can be achieved. The aim of the present study was to examine the influence of stimulus predictability, target velocity, and interstimulus interval (ISI) on ocular pursuit during the transient disappearance of a visual target. We confirmed that subjects (n = 9) did not maintain eye velocity close to target velocity for the duration of the ISI. In general, after an initial reduction in eye velocity the majority of subjects (n = 7) exhibited a significant increase before target reappearance. The timing of the velocity increase was not influenced by target velocity, stimulus predictability, or ISI. Consequently, for the 900-ms ISI the increase occurred too early and the eye was decelerating at the moment of target reappearance. These results are consistent with a reduction in gain being applied to the visuomotor drive when the target disappeared, followed by a reactivation in expectation of target reappearance. We modeled this process such that gain was modulated within a reafferent feedback system, hence preserving its output in the absence of negative visual feedback and enabling an anticipatory increase in eye velocity before expected target reappearance.

Adult↗

Anticipatory responses to perturbation of co-ordination in one-handed catching.

Anticipatory responses to perturbation have rarely been studied in the co-ordination of dynamic interceptive actions. In this study, the kinematics of ball catching were examined in skilled catchers when mechanical perturbation of the catching arm was expected and unexpected. During trials where the perturbation was anticipated, participants initiated movements earlier (207 +/- 32 ms) than in randomly perturbed trials (223 +/- 34 ms). Furthermore, several individuals also tended to move their hand faster when perturbations were expected compared to baseline trials. Individual analyses revealed that three out of eight participants exhibited changes in the relative timing of the grasp phase to adapt to the specific manipulation of task constraints. Anticipatory responses were revealed in changes not only at movement initiation but also in the resulting adaptations to the co-ordination of reach and grasp phases of ball catching. When the catchers could not anticipate perturbations, movement strategies suggested the use of a continuous tracking-based mode of control rather than a prediction-based mode of control.

Adult↗

Effect of verbal instructions and image size on visual search strategies in basketball free throw shooting.

We assessed the effects on basketball free throw performance of two types of verbal directions with an external attentional focus. Novices (n = 16) were pre-tested on free throw performance and assigned to two groups of similar ability (n = 8 in each). Both groups received verbal instructions with an external focus on either movement dynamics (movement form) or movement effects (e.g. ball trajectory relative to basket). The participants also observed a skilled model performing the task on either a small or large screen monitor, to ascertain the effects of visual presentation mode on task performance. After observation of six videotaped trials, all participants were given a post-test. Visual search patterns were monitored during observation and cross-referenced with performance on the pre- and post-test. Group effects were noted for verbal instructions and image size on visual search strategies and free throw performance. The 'movement effects' group saw a significant improvement in outcome scores between the pre-test and post-test. These results supported evidence that this group spent more viewing time on information outside the body than the 'movement dynamics' group. Image size affected both groups equally with more fixations of shorter duration when viewing the small screen. The results support the benefits of instructions when observing a model with an external focus on movement effects, not dynamics.

Adult↗

Postural sway and active balance performance in highly active lower-limb amputees.

OBJECTIVE: To determine the balance performance of active lower-limb amputees during quiet standing and under dynamic conditions. DESIGN: Center-of-pressure excursions during quiet standing and the standing balance performance on a single axis stabilimeter was assessed in six unilateral lower-limb amputees and six able-bodied controls. Stabilimeter trials were repeated with subjects standing so that pivoting occurred either in the anteroposterior or mediolateral direction or in the mediolateral direction but with vision occluded. RESULTS: Center-of-pressure excursions were significantly greater (P < 0.05) for amputees in both the mediolateral and anteroposterior directions. During all stabilimeter tests, amputees spent significantly less time in balance than able-bodied controls (P < 0.05), and this was attributed to a nonsignificant increase in the average time the stabilimeter spent in contact with the ground. Group differences in the average time of contact in the anteroposterior test condition were meaningful (effect size, 1.19). CONCLUSIONS: Amputees had poorer static and dynamic balance than able-bodied controls. Amputees had a greater problem controlling dynamic balance in the anteroposterior direction than the mediolateral direction. Findings highlight the importance of the ankle in maintaining balance in situations that involve body movements in the sagittal plane.

Adult↗

Vertical jump coordination: fatigue effects.

PURPOSE: The aim of this study was to investigate the segmental coordination of vertical jumps under fatigue of the knee extensor and flexor muscles. METHODS: Eleven healthy and active subjects performed maximal vertical jumps with and without fatigue, which was imposed by requesting the subjects to extend/flex their knees continuously in a weight machine, until they could not lift a load corresponding to approximately 50% of their body weight. Knee extensor and flexor isokinetic peak torques were also measured before and after fatigue. Video, ground reaction forces, and electromyographic data were collected simultaneously and used to provide several variables of the jumps. RESULTS: Fatiguing the knee flexor muscles did not reduce the height of the jumps or induce changes in the kinematic, kinetic, and electromyographic profiles. Knee extensor fatigue caused the subjects to adjust several variables of the movement, in which the peak joint angular velocity, peak joint net moment, and power around the knee were reduced and occurred earlier in comparison with the nonfatigued jumps. The electromyographic data analyses indicated that the countermovement jumps were performed similarly, i.e., a single strategy was used, irrespective of which muscle group (extensor or flexors) or the changes imposed on the muscle force-generating characteristics (fatigue or nonfatigue). The subjects executed the movements as if they scaled a robust template motor program, which guided the movement execution in all jump conditions. It was speculated that training programs designed to improve jump height performance should avoid severe fatigue levels, which may cause the subjects to learn and adopt a nonoptimal and nonspecific coordination solution. CONCLUSION: It was suggested that the neural input used in the fatigued condition did not constitute an optimal solution and may have played a role in decreasing maximal jump height achievement.

Adult↗