An object for an action, the same object for other actions: effects on hand shaping (original) (raw)
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Effects of End-Goal on Hand Shaping
Journal of Neurophysiology, 2006
The aim of the present study was to determine whether hand shaping was affected by planning of an action subsequent to object contact. Ten subjects (5 females and 5 males, ages 19-33) were requested to reach toward and grasp a convex object between the thumb and the four fingers of the right hand and to perform one of the following actions: 1) lift up the object; 2) insert the object into a niche of a similar shape and size as the object, or 3) insert the object into a rectangular niche much larger than the object. Flexion/extension at the metacarpal-phalangeal and proximal interphalangeal joints of all digits were measured using resistive sensors embedded in a glove. Although all experimental conditions required grasping the same object, we found different covariation patterns among finger joint angles across conditions. Gradual preshaping of the hand occurred only when planning object lift or when the end-goal required object placement into the tight niche. In contrast, for the larger niche, gradual preshaping was not evident for the ring and the little finger. Further, reaching movements were faster for movements ending with the larger niche than for the other movement conditions. The present results suggest that hand shaping takes into account end-goal in addition to object geometry. We discuss these findings in the context of forward internal models that allow the prediction of the sensorimotor consequences of motor commands in advance to their execution.
Distractor objects affect fingers' angular distances but not fingers' shaping during grasping
2007
The aim of the present study was to determine whether and how hand shaping was affected by the presence of a distractor object adjacent to the tobe-grasped object. Twenty subjects were requested to reach towards and grasp a 'convex' or a 'concave' object in the presence or absence of a distractor object either of the same or different shape than the target object. Flexion/extension at the metacarpal-phalangeal (MCP) and proximal interphalangeal joints of all digits, and abduction angle between digits were measured by resistive sensors embedded in a glove. The results indicate robust interference effects at the level of reach duration and the extent of fingers' abduction angles together with changes at the level of a single joint for the thumb. No distractor effects on individual fingers' joints except for the MCP of the middle and little fingers were found. These findings suggest that the presence of distractor object affects hand shaping in terms of fingers' abduction angles, but not at the level of 'shape dependent' fingers' angular excursions. Furthermore, they support the importance of the thumb for the guidance of selective reach-to-grasp movements. We discuss these results in the context of current theories proposed to explain the object selection processes underlying the control of hand action. C. Ansuini Á V. Tognin Á L. Turella Á
Grasp With Hand and Mouth: A Kinematic Study on Healthy Subjects
Journal of Neurophysiology, 2001
Neurons involved in grasp preparation with hand and mouth were previously recorded in the premotor cortex of monkey. The aim of the present kinematic study was to determine whether a unique planning underlies the act of grasping with hand and mouth in humans as well. In a set of four experiments, healthy subjects reached and grasped with the hand an object of different size while opening the mouth ( experiments 1 and 3), or extending the other forearm ( experiment 4), or the fingers of the other hand ( experiment 5). In a subsequent set of three experiments, subjects grasped an object of different size with the mouth, while opening the fingers of the right hand ( experiments 6–8). The initial kinematics of mouth and finger opening, but not of forearm extension, was affected by the size of the grasped object congruently with the size effect on initial grasp kinematics. This effect was due neither to visual presentation of the object, without the successive grasp motor act ( experimen...
Task Requirements Influence Sensory Integration During Grasping in Humans
Learning & Memory, 2004
The sensorimotor transformations necessary for generating appropriate motor commands depend on both current and previously acquired sensory information. To investigate the relative impact (or weighting) of visual and haptic information about object size during grasping movements, we let normal subjects perform a task in which, unbeknownst to the subjects, the object seen (visual object) and the object grasped (haptic object) were never the same physically. When the haptic object abruptly became larger or smaller than the visual object, subjects in the following trials automatically adapted their maximum grip aperture when reaching for the object. This adaptation was not dependent on conscious processes. We analyzed how visual and haptic information were weighted during the course of sensorimotor adaptation. The adaptation process was quicker and relied more on haptic information when the haptic objects increased in size than when they decreased in size. As such, sensory weighting seemed to be molded to avoid prehension error. We conclude from these results that the impact of a specific source of sensory information on the sensorimotor transformation is regulated to satisfy task requirements.
Interlimb Transfer of Grasp Orientation is Asymmetrical
The Scientific World JOURNAL, 2006
One the most fundamental aspects of the human motor system is the hemispheric asymmetry seen in behavioral specialization. Hemispheric dominance can be inferred by a contralateral hand preference in grasping. Few studies have considered grasp orientation in the context of manual lateralization and none has looked at grasp orientation with natural prehension. Thirty right-handed adults performed precision grasps of a cylinder using the thumb and index fingers, and the opposition axis (OA) was defined as the line connecting these two contact points on the cylinder. Subjects made ten consecutive grasps with one hand (primary hand movements) followed by ten grasps with the other hand (trailing movements). Differences between primary and trailing grasps revealed that each hemisphere is capable of programming the orientation of the OA and that primary movements with the right hand significantly influenced OA orientation of the trailing left hand. These results extend the hemispheric dominance of the left hemisphere to the final positions of fingers during prehension.
Orientation of the opposition axis in mentally simulated grasping
Experimental Brain Research, 2001
Five normal subjects were tested in a simulated grasping task. A cylindrical container filled with water was placed on the center of a horizontal monitor screen. Subjects used a precision grip formed by the thumb and index finger of their right hand. After a preliminary run during which the container was present, it was replaced by an image of the upper surface of the cylinder appearing on the horizontal computer screen on which the real cylinder was placed during the preliminary run. In each trial the image was marked with two contact points which defined an opposition axis in various orientations with respect to the frontal plane. The subjects' task consisted, once shown a stimulus, of judging as quickly as possible whether the previously experienced action of grasping the container full of water and pouring the water out would be easy, difficult or impossible with the fingers placed according to the opposition axis indicated on the circle. Response times were found to be longer for the grasps judged to be more difficult due to the orientation and position of the opposition axis. In a control experiment, three subjects actually performed the grasps with different orientations and positions of the opposition axis. The effects of these parameters on response time followed the same trends as during simulated movements. This result shows that simulated hand movements take into account the same biomechanical limitations as actually performed movements.
Viewing objects and planning actions: On the potentiation of grasping behaviours by visual objects
Brain and cognition, 2011
How do humans interact with tools? Gibson (1979) suggested that humans perceive directly what tools afford in terms of meaningful actions. This “affordances” hypothesis implies that visual objects can potentiate motor responses even in the absence of an intention to act. Here we explore the temporal evolution of motor plans afforded by common objects. We presented objects that have a strong significance for action (pinching and grasping) and objects with no such significance. Two experimental tasks involved participants viewing objects presented on a computer screen. For the first task, they were instructed to respond rapidly to changes in background colour by using an apparatus mimicking precision and power grip responses. For the second task, they received stimulation of their primary motor cortex using transcranial magnetic stimulation (TMS) while passively viewing the objects. Muscular responses (motor evoked potentials: MEPs) were recorded from two intrinsic hand muscles (associated with either a precision or power grip). The data showed an interaction between type of response (or muscle) and type of object, with both reaction time and MEP measures implying the generation of a congruent motor plan in the period immediately after object presentation. The results provide further support for the notion that the physical properties of objects automatically activate specific motor codes, but also demonstrate that this influence is rapid and relatively short lived.► How do objects automatically activate specific motor plans known as “affordances”? ► Task-irrelevant pictures shown to activate congruent grip actions. ► Affordance effect evident in both RTs and motor evoked potentials. ► Affordance effect arises rapidly and also dissipates quickly. ► Affordance effect evident for separate hand actions generated in the same hemisphere.