Quando um estímulo ocorre aleatoriamente à esquerda ou à direita do ponto de fi xação, a resposta é mais rápida quando o estímulo e a tecla de resposta estão do mesmo lado (condição compatível) do que quando estão em lados opostos (condição incompatível

Simple manual reaction time (MRT) to a visual target (S2) is shortened when a non-informative cue (S1) is flashed at the S2 location shortly before the onset of S2 (early facilitation). Afterwards, MRT to S2 appearing at the S1 location is lengthened (inhibition of return -IOR). Similar results have been obtained for saccadic reaction time (SRT). Moreover, when there is a temporal gap between offset of the fixation point (FP) and onset of a target (gap paradigm), SRT is shorter than SRT in an overlap paradigm (FP remains on). In the present study, we determined SRT to S2 (10º) after presenting S1 at the same eccentricity (10º) or at a parafoveal position (2º) in the same or in the opposite hemifield. In addition, we employed both gap and overlap paradigms. Twelve subjects were asked not to respond to S1 (2º or 10º) to the right or to the left of FP, but to respond by making a saccadic movement in response to S2. We obtained the following results: 1) a 40-ms gap effect, 2) an interaction between gap effect and IOR, 3) a 39-ms delay (IOR) when S2 appeared at the cued (S1) position, and 4) a smaller (17 ms) but significant inhibition when S1 occurred at 2º in the ipsilateral hemifield. Thus, a parafoveal (2º) S1 elicits an inhibition of SRT towards ipsilateral peripheral targets. Since an inhibition of the ipsilateral hemifield by a 1º eccentric cue has been reported to occur when manual responses are employed, we suggest that the postulated functional link between covert and overt orienting of attention is also valid for parafoveal cues.

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The handedness recognition of visually perceived body parts engages motor representations that are constrained by the same biomechanical factors that limit the execution of real movements. In the present study, we used small plastic cutouts that represented the human hand to investigate the properties of mental images generated during their haptic exploration. Our working hypothesis was that any handedness recognition task that involves body parts depends on motor imagery. Forty-four blindfolded, right-handed volunteers participated in a handedness evaluation experiment using their index finger to explore either the back or palm view of a haptic stimulus that represented the human hand. The stimuli were presented in four different orientations, and we measured the subjects' response times. Our results showed that stimulus configurations that resemble awkward positions of the human hand are associated with longer response times (p < .006), indicating that the haptic exploration of stimuli that represent body parts also leads to motor imagery that is constrained by biomechanical factors.

The visual recognition of body parts activates somato-motor representations in the brain. In the present study, we investigate the influence of the plane in which hand drawings are displayed (Vertical or Horizontal) on mental rotations evoked by a handedness recognition task. Sixteen right-handed volunteers participated in an experiment where the task was to evaluate the handedness of drawings of the human hand presented in different perspectives and orientations while the Manual Reaction Time (MRT) was measured. For eight volunteers, the hand drawings were displayed on a vertical screen monitor, while for the remainder a mirror was employed and the same drawings appeared on the horizontal plan. Our main finding was that there are no differences in MRTs among the drawings displayed vertically or horizontally, with some exceptions. However, the MRTs were longer when the hands in the drawings assumed configurations that were more awkward to perform using real movements. These results show that the implicit movements involved with handedness recognition are mainly dependent on biomechanical constraints for distal (hand), but not proximal (shoulder) movements.