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    Disadvantageous associations: Reversible spatial cueing effects in a discrimination task

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    Current theories describe learning in terms of cognitive or associative mechanisms. To assess whether cognitive mechanisms interact with automaticity of associative processes we devised a shape-discrimination task in which participants received both explicit instructions and implicit information. Instructions further allowed for the inference that a first event would precede the target. Albeit irrelevant to respond, this event acted as response prime and implicit spatial cue (i.e. it predicted target location). To modulate cognitive involvement, in three experiments we manipulated modality and salience of the spatial cue. Results always showed evidence for a priming effect, confirming that the first stimulus was never ignored. More importantly, although participants failed to consciously recognize the association, responses to spatially cued trials became either slower or faster depending on salience of the first event. These findings provide an empirical demonstration that cognitive and associative learning mechanisms functionally co-exist and interact to regulate behaviour

    Grasping an illusion

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    In the present study we attempted to determine the nature of the visual analysis that is performed on an object in order to grasp it. We required eight healthy subjects to reach and grasp a wooden bar which was superimposed over the shaft of the Müller-Lyer illusion. Vision of both the hand and the bar was allowed. Three different bar lengths were used. Two additional control tasks in which the subjects were required to reproduce the length of the shafts were carried out. The results showed that hand shaping while grasping the bar was influenced by the illusion configurations on which it was superimposed. However, this effect was smaller than that observed in the two tasks of length reproduction. These results support the notion that visual analysis performed on the object of a grasp movement is global and takes into account the object itself, as well as its relationships with surrounding cues. We propose, as suggested previously for reaching movements (Gentilucci, M. et al., Neuropsychologia, 1996, 34, 369-376), two partially independent stages during visuo-motor integration for grasping an object. In the first stage, the object is coded inside an object-centred frame of reference. In the second stage it is transposed in an egocentric frame of reference, in which the spatial relations between object and agent are computed. In this second stage the influence of cues surrounding the target is minimized

    Haptic information differentially interferes with visual analysis in reaching-grasping control and in perceptual processes

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    We used an interference paradigm in order to study integration between haptic and visual information in motor control and in perceptual analysis. Subjects either reached and grasped a visually presented sphere or matched its size with their left hand while manipulating with their right hand another sphere whose size could be smaller or greater. In four experiments haptic analysis of the manipulated sphere could be either automatically incorporated with or explicitly dissociated from visual analysis. In a fifth experiment reaching-grasping and matching were executed with the right hand, whereas manipulation was executed with the left hand. Manipulation with the right hand influenced finger shaping during grasping with the left hand when the sizes of the two objects were different. Interference was observed mainly in those experiments in which haptic analysis could be automatically integrated with visual analysis. In the matching task, no effect was observed. Finally, manipulation with the left hand did not produce any interference effect on reaching-grasping and matching executed by the right hand. The results of the present study suggest that somesthetic information is integrated with visual information only in sensorimotor transformations. In addition, they support the notion that the left hemisphere together with the right hemisphere is involved in the control of left hand reaching-grasping movements

    Visual distractors differentially interfere with the reaching and grasping components of prehension movements

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    In the present study we addressed the issue of how an object is visually isolated from surrounding cues when a reaching-grasping (prehension) movement towards it is planned. Subjects were required to reach and grasp an object presented either alone or with a distractor. In five experiments, different degrees of elaboration of the distractor were induced by varying: (1) the position of the distractor (central or peripheral); (2) the time when the distractor was suppressed (immediately or delayed, with respect to stimulus presentation); and (3) the type of distractor analysis (implicit or explicit). In addition, we tested whether the possible effects of the distractor on reaching-grasping were due to the use of an allocentric reference centered on it. This was obtained by comparing the effects of the distractor with those of a stimulus, the target of a placing movement successive to the reaching-grasping. The results of the five experiments can be summarized as follows. The necessary condition for an interference effect on both the reaching and the grasping components was the central presentation of the distractor. When the information on the distractor could be immediately suppressed, an interference effect was observed only on the grasp component. In the case of delayed suppression, an effect was found on the reaching component. Finally, when an overt analysis of the distractor was required, the interference effect disappeared. Two main conclusions have been drawn from the results of the present study. First, comparison between properties of the target and surrounding cues is performed by two independent processes for reaching and grasping an object. The process for the grasp relies more on allocentric cues than that for the reach. Second, when surrounding stimuli are automatically analyzed during visual search of the target, the process of visuo-motor transformation can incorporate their features into the target. In contrast, overt analysis of surrounding stimuli is performed separately from that of the target. Finally, the data of the present study are discussed in support of the premotor theory of attention

    Implicit visual analysis in handedness recognition

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    In the present study, we addressed the problem of whether hand representations, derived from the control of hand gesture, are used in handedness recognition. Pictures of hands and fingers, assuming either common or uncommon postures, were presented to right-handed subjects, who were required to judge their handedness. In agreement with previous results (Parsons, 1987, 1994; Gentilucci, Daprati, & Gangitano, 1998), subjects recognized handedness through mental movement of their own hand in order to match the posture of the presented hand. This was proved by a control experiment of physical matching. The new finding was that presentation of common finger postures affected responses differently from presentation of less common finger postures. These effects could be not attributed to mental matching movements nor related to richness in hand-finger cues useful for handedness recognition. The results of the present study are discussed in the context of the notion that implicit visual analysis of the presented hands is performed before mental movement of one's hand takes place (Parsons, 1987; Gentilucci et al., 1998). In this process, hand representation acquired by experience in the control and observation of one's and other people's hand gestures is used. We propose that such an immediate recognition mechanism belongs to the class of mental processes which are grouped under the name of intuition, that is, the processes by which situations or people's intentions are immediately understood, without conscious reasoning

    Right-handers and left-handers have different representations of their own hand

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    The visual control of our own hand when dealing with an object and the observation of interactions between other people's hand and objects can be involved in the construction of internal representations of our own hand, as well as in hand recognition processes. Therefore, a different effect on handedness recognition is expected when subjects are presented with hands holding objects with either a congruent or an incongruent type of grip. Such an experiment was carried out on right-handed and left-handed subjects. We expected that the different degree of lateralisation in motor activities observed in the two populations [J. Herron, Neuropsychology of left-handedness, Academic Press, New York, 1980.] could account for the construction of different internal hand representations. As previously found [L.M. Parsons, Imaged spatial transformations of one's hands and feet, Cogn. Psychol., 19 (1987) 178-241.], in order to identify handedness, subjects mentally rotated their own hand until it matched with the presented one. This process was confirmatory, being preceded by an implicit visual analysis of the target hand. Presentation of hands holding objects with congruent or incongruent types of grip influenced handedness recognition at different stages in right-handed and left-handed subjects. That is, the mental rotation stage was affected in right-handed subjects, whereas the initial phase of implicit hand analysis was affected in left-handed subjects. We suggest that in handedness recognition, left-handers relied more on a pictorial hand representation, whereas right-handers relied more on a pragmatic hand representation, probably derived from experience in the control of their own movements. The use of different hand representations may be due to differential activation of temporal and premotor areas

    Tactile input of the hand and the control of reaching to grasp movements.

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    The role of tactile information of the hand in the control of reaching to grasp movements was investigated. The kinematics of both reaching (or transport) and grasp components were studied in healthy subjects in two experimental conditions. In one condition (control condition) subjects were required to reach and grasp an object that could have two sizes and that could be located at two distances from the viewer. In the other condition (anaesthesia condition) the same movements were executed, but anaesthesia was provided to the subjects' fingertips. In both conditions vision of the hand was prevented during movement. Anaesthesia affected mainly the kinematics of the first phase of grasping, that is, the finger-opening phase. This phase was lengthened and maximal finger aperture increased. In contrast, the duration of the successive phase (finger-closure) was poorly modified. The reaching component was also impaired by anaesthesia. Although the total extent of hand path and the spatial relations between the finger aperture and closure phases did not change between the two conditions, hand path variability increased. This occurred during transport deceleration phase and after the increase in variability of finger path. In addition, the whole movement was slowed down. The results of the present experiment suggest that tactile signals at the beginning and at the end of movement can be used to compute grasp time and to optimise grasp temporal parameters. Alternatively, signals from tactile receptors can be involved in encoding the position sense of the fingers. When this input is lacking, the control of grasp and in particular that of finger-opening phase can be impaired. Finally, the effect of the grasp impairment on the reaching component supports the notion that the coordination between reaching and grasping involves the whole temporal course of the two components
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