On-line versus off-line control of rapid aiming movements

Recent studies have shown the importance of visual feedback during the rapid initial phase of aiming movements for the control of direction (e.g., Bard, Paillard, Fleury, Hay, & Larue, 1990; Blouin, Teasdale, Bard, & Fleury, in press; Teasdale, Blouin, Bard, & Fleury, 1991). In most of these studies, visual feedback conditions were presented in blocked sessions. Consequently, higher-order processes (e.g., feedforward and/or learning processes), along with on-line processing of visual feedback, might have contributed to the better accuracy found when subjects had visual feedback of only the initial portion of the movements (compared with movements without visual feedback). To test this possibility, we studied subjects' performance of rapid arm movements under different types of presentation (random, precued, and blocked) of the visual feedback conditions of the trajectory (no vision, initial portion only, and vision of the entire trajectory). Directional errors were larger in the no-vision condition than in both conditions with visual feedback. There were no differences among the presentation conditions, suggesting that on-line processing of visual information contributed to the control of the arm movements.     

Behavior Matching in Multimodal Communication Is Synchronized

A variety of theoretical frameworks predict the resemblance of behaviors between two people engaged in communication, in the form of coordination, mimicry, or alignment. However, little is known about the time course of the behavior matching, even though there is evidence that dyads synchronize oscillatory motions (e.g., postural sway). This study examined the temporal structure of nonoscillatory actions—language, facial, and gestural behaviors—produced during a route communication task. The focus was the temporal relationship between matching behaviors in the interlocutors (e.g., facial behavior in one interlocutor vs. the same facial behavior in the other interlocutor). Cross‐recurrence analysis revealed that within each category tested (language, facial, gestural), interlocutors synchronized matching behaviors, at temporal lags short enough to provide imitation of one interlocutor by the other, from one conversational turn to the next. Both social and cognitive variables predicted the degree of temporal organization. These findings suggest that the temporal structure of matching behaviors provides low‐level and low‐cost resources for human interaction.     

Resolving Power of the Perceptual-and Sensorimotor Systems in 6- to 10-Year-Old Children

Children aged 6 to 10 were tested on their ability to move accurately and to perceptually evaluate their motor response. Subjects performed a directional and an amplitude visuo-manual aiming task without vision of their moving limb. They were asked to correct their error, after completion of their movements, only if they felt they were not accurate. Terminal aiming errors and correction responses (adjustments) were analyzed, and threshold detection was determined relative to terminal aiming error. Action accuracy and evaluation of action accuracy are two abilities that do not develop synchronously. Moreover, the relationship between these abilities depends on whether accuracy and direction or amplitude are required. Amplitude undergoes more corrections than direction, suggesting that the spatial system of reference involved depends more upon the coding of the final position than on direction. Two spatial comparators, operating on the basis of two types of evaluation, seem to have a variably distinct contribution to movement and perception accuracy, according to age.     

The attentional cost of amplitude and directional requirements when pointing to targets

The aim of this study was to investigate the comparative cost of accuracy constraints in direction or amplitude for movement regulation. The attentional cost is operationally defined as the amount of disturbance created in a secondary task by the simultaneous execution of a pointing task in direction or amplitude. The cost is expressed in terms of modifications in response to a secondary task, consisting of a foot-pedal release in response to an auditory stimulus (probe). The probe was introduced during the programming portion or the first, middle, or last portion of the pointing movement. The independent variables were the requirements of the task: direction or amplitude, and the moments of occurrence of the probe. Subjects were submitted to eight experimental conditions: (1) simple foot reaction time to a buzzer; (2) single directional task; (3) single amplitude task; (4) dual directional task (i.e. directional task with probe); (5) dual amplitude task (i.e. amplitude task with probe); (6) retest of foot simple reaction time; (7) retest of single directional task; and (8) retest of single amplitude task. Regulation in direction was more attention-demanding than regulation in distance in terms of programming. During pointing in amplitude, probe RT increased monotonically from start to end of movement execution, whereas directional pointing did not lead to any significant probe RT changes. These results emphasize the specific attentional loads for directional and amplitude pointing tasks, hence the involvement of different central nervous system mechanisms for the programming and regulation of the directional and amplitude parameters of pointing movements.     

Abstract: A Multi-Level Model of Individual Differences in Speed/Accuracy Tradeoff (SATin)

Individuals performing an experimental cognitive task have a choice whether to favor accuracy, speed, or weight them both equally. Models of speed/ accuracy tradeoff have been proposed in the assessment literature (van der Linden, 2007 van der Linden, W. J. 2007. A hierarchical framework for modeling speed and accuracy on test items. Psychometrika, 72: 287–308. [Crossref], [Web of Science ®] , [Google Scholar]) and experimental literature (Ratcliff &; Rouder, 1998 Ratcliff, R. and Rouder, J. N. 1998. Modeling response times for two-choice decisions.. Psychological Science, 9: 347–357. [Crossref], [Web of Science ®] , [Google Scholar]). However, these models do not estimate individual differences in choice of speed/ accuracy tradeoff at between- and within-subjects levels.

The top of Figure 1 presents the equations and path diagram for the SATin model. Individual differences in speed/ accuracy tradeoff will be modeled at two levels with, 1) variability in Tradeoff (between-subject level, Level 2) and 2) variability in c (within-subject level, Level 1). An individual's Tradeoff factor score represents the individual's distributional position relative to others regarding whether they favor speed (values < 0), accuracy (values > 0), or neither (value = 0). A negative c indicates that the individual is trading off speed and accuracy for these particular trials, whereas a positive and zero c indicate the individual is not trading off.

Abstract: A Multi-Level Model of Individual Differences in Speed/Accuracy Tradeoff (SATin)

All authors

Dan R. Johnson, William H. Beasley &; David E. Bard

https://doi.org/10.1080/00273170802640475

Published online:

18 December 2008

FIGURE 1 SATin Model Diagram.     

27.

The effects of spatial movement components precues on the execution of rapid aiming in children aged 7, 9, and 11     

Olivier I  Bard C 《Journal of experimental child psychology》2000,77(2):155-168

The aim of the present study was twofold: first, to investigate the effects of spatial precues on the execution of rapid aiming in children aged 7, 9, and 11 and second, to provide a kinematic support to the investigation of the role of precues in aiming tasks performed under temporal constraints. Four precuing conditions were used, where participants received: (a) no precue of any type, (b) advance information on direction, (c) advance information on amplitude, and (d) complete information on the forthcoming movement. Our results showed that precuing the spatial dimensions of movement shortens reaction times, that such shortening is a function of the number of precued parameters, and that spatial precues modify the kinematics of the children's rapid aiming movements. Peak velocity increased with direction and/or amplitude, suggesting that precues play a significant role in motor preparation. Moreover, the accuracy results indicate that direction precuing induces a proactive directional regulation. Finally, direction and amplitude appear to be independently specified in children.     

28.

Control of Rapid Arm Movements When Target Position Is Altered During Saccadic Suppression     

Blouin J  Teasdale N  Bard C  Fleury M 《Journal of motor behavior》1995,27(2):114-122

This experiment examined whether rapid arm movements can be corrected in response to a change in target position that occurs just prior to movement onset, during saccadic suppression of displacement. Because the threshold of retinal input reaches its highest magnitude at that time, displacement of the visual target of a saccade is not perceived. Subjects (N = 6) were instructed to perform very rapid arm movements toward visual targets located 16, 20, and 24 degrees from midline (on average, movement time was 208 ms). On some trials the 20 degrees target was displaced 4 degrees either to the right or to the left during saccadic suppression. For double-step trials, arm movements did not deviate from their original trajectory. Movement endpoints and movement structure (i.e., velocity-and acceleration-time profiles) were similar whether or not target displacements occurred, showing the failure of proprioceptive signals or internal feedback loops to correct the arm trajectory. Following this movement, terminal spatially oriented movements corrected the direction of the initial movement (as compared with the single-step control trials) when the target eccentricity decreased by 4 degrees. Subjects were unaware of these spatial corrections. Therefore, spatial corrections of hand position were driven by the goal level of the task, which was updated by oculomotor corrective responses when a target shift occurred.     

29.

The recognition of words after their acoustic offsets in spontaneous speech: effects of subsequent context     

E G Bard  R C Shillcock  G T Altmann 《Perception & psychophysics》1988,44(5):395-408

     

30.

Why Evolution Matters: a Jewish view     

Jonathan Bard 《Journal of Modern Jewish Studies》2013,12(2):347-348

     

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The effects of spatial movement components precues on the execution of rapid aiming in children aged 7, 9, and 11

The aim of the present study was twofold: first, to investigate the effects of spatial precues on the execution of rapid aiming in children aged 7, 9, and 11 and second, to provide a kinematic support to the investigation of the role of precues in aiming tasks performed under temporal constraints. Four precuing conditions were used, where participants received: (a) no precue of any type, (b) advance information on direction, (c) advance information on amplitude, and (d) complete information on the forthcoming movement. Our results showed that precuing the spatial dimensions of movement shortens reaction times, that such shortening is a function of the number of precued parameters, and that spatial precues modify the kinematics of the children's rapid aiming movements. Peak velocity increased with direction and/or amplitude, suggesting that precues play a significant role in motor preparation. Moreover, the accuracy results indicate that direction precuing induces a proactive directional regulation. Finally, direction and amplitude appear to be independently specified in children.     

Control of Rapid Arm Movements When Target Position Is Altered During Saccadic Suppression

This experiment examined whether rapid arm movements can be corrected in response to a change in target position that occurs just prior to movement onset, during saccadic suppression of displacement. Because the threshold of retinal input reaches its highest magnitude at that time, displacement of the visual target of a saccade is not perceived. Subjects (N = 6) were instructed to perform very rapid arm movements toward visual targets located 16, 20, and 24 degrees from midline (on average, movement time was 208 ms). On some trials the 20 degrees target was displaced 4 degrees either to the right or to the left during saccadic suppression. For double-step trials, arm movements did not deviate from their original trajectory. Movement endpoints and movement structure (i.e., velocity-and acceleration-time profiles) were similar whether or not target displacements occurred, showing the failure of proprioceptive signals or internal feedback loops to correct the arm trajectory. Following this movement, terminal spatially oriented movements corrected the direction of the initial movement (as compared with the single-step control trials) when the target eccentricity decreased by 4 degrees. Subjects were unaware of these spatial corrections. Therefore, spatial corrections of hand position were driven by the goal level of the task, which was updated by oculomotor corrective responses when a target shift occurred.