The present study investigated the influence of emotional valence on the spatial stimulus-key location correspondence effect in three experiments using the Affective Spatial Correspondence task (AffSCt). We initially reanalyzed the results of Conde et al. (2011) according to the model proposed by Proctor (2013). In that study, compatible and incompatible responses were chosen according to the participants' team preference. In one block, the volunteers had to press a key on the same side for the Favorite team and on the opposite side for the Rival team. In another block, a reverse code was used. We found that responses were faster for the Favorite-compatible/Rival-incompatible condition (614 ms) compared with the Favorite-incompatible/Rival-compatible condition (691 ms). The same experimental arrangement was replicated in another Brazilian city, and similar results were found. Additionally, we employed non-affective "fake" soccer teams as a control condition, and no mapping-rule effect was observed. Finally, a final experiment that used the same design but different non-affective stimuli (yellow and blue bars) was performed to provide further evidence that the valence effect in the present experimental paradigm only occurs with affective stimuli. As expected, non-affective stimuli did not produce an overall advantage for any mapping rules, corroborating earlier findings with similar mixed designs. The results confirmed the previous findings and validity of the AffSCt as a methodology to investigate the effects of emotional valence on stimulus-response correspondence. However, we are unable to provide a conclusive explanation to support the several hypotheses proposed previously in our paper and by Proctor (2013).

A visual stimulus (e.g., a letter, word, or object) may have a lasting effect on the processing of subsequent stimuli. The present study verified the priming effect of a figure (i.e., five-petal daisy) on manual reaction time (MRT) to another equal or different five-petal daisy. Two distinct groups were tested. One group was instructed that the five-petal daisy represented a human hand. The other group was instructed that the five-petal daisy represented a flower. The figures in the pairs of stimuli could share or not share some features such as handedness and view. In both groups, after being informed whether the five-petal daisy represented a flower or human hand, an uninformative flower was presented for 200 ms in the center of the screen. After 1000 ms, a second flower was presented in the same location until the observer responded by pressing a left or right switch. The results showed that prior presentation of the five-petal daisy affected MRT only when the figure represented a human hand. Furthermore, an opposite effect of view on MRT was found. The shorter MRT to the back (dorsal) view of the figure that represented a human hand could be attributable to a faster response to the dorsal view of a hand figure made with a prone posture of the participants' hand than to a front (palm) view. The longer MRT to the back view of the figure that represented a flower may be due to a mental rotation of the object along its vertical axis before selecting the correct response because the response was based on the position of the asymmetrical petal in the canonical front view of the daisy.

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.

Os tempos de reação manuais e sacádicos (TRMs e TRSs) são reduzidos quando um sinal de aviso precede o aparecimento do alvo. O decréscimo nos TRSs observados depois do desaparecimento do ponto de fixação tem sido chamado de efeito de intervalo. Teorias diferentes foram propostas para explicá-lo. De acordo com alguns autores, o desaparecimento também permite ao sistema sacádico gerar uma população separada de TRSs, as sacádicas expressas. No entanto, não há concordância sobre a influência do desaparecimento de um estímulo periférico no TRM. Em dois experimentos, testou-se os efeitos de um desaparecimento visual periférico empregado como um sinal preparatório para os TRMs a um alvo, após intervalos variáveis. Encontrou-se uma redução no TRM para intervalos curtos (200-300 ms) e longos (1300-2000 ms) após o desaparecimento periférico. A distribuição dos TRMs deslocou-se para latências curtas, formando por vezes populações separadas. Visto que os TRMs obtidos em intervalos longos foram afetados pela introdução de sessões capciosas, enquanto que os TRMs em intervalos curtos não o foram, propõe-se que dois mecanismos diferentes estão envolvidos no decréscimo dos TRMs: alerta e expectativa temporal. Nossos dados sustentam a hipótese de que o componente temporal envolvido com os estágios preparatórios das respostas motoras podem ser compartilhados pelos movimentos sacádicos e pelas respostas de apertar botões, permitindo a redução das latências motoras após o desaparecimento visual, dentro do paradigma do intervalo. Nossos dados corroboram o modelo de três componentes do efeito de intervalo. Em nosso ponto de vista, a questão da existência ou não do efeito de intervalo para respostas manuais é essencialmente conceitual.

Manual and saccadic reaction times (MRTs and SRTs) are reduced when a warning signal precedes the onset of a target. The decreasing on SRTs observed after the offset of a fixation point has been called the gap effect. Different theories have been proposed to explain it. According to some authors, the offset also allows the saccadic system to generate a separate population of SRTs, the express saccades. Nevertheless there is no agreement about the influence of the offset of a peripheral stimulus on MRT. In two experiments we tested the effects of a peripheral visual offset used as preparatory signal on MRTs to a target after variable intervals. We found a reduction on MRT at short (200-300 ms) and long (1300-2000 ms) intervals after the peripheral offset. MRT distribution shifted toward short latencies, which sometimes formed a separate population. Since MRTs obtained at long intervals were affected by the introduction of catch trials, while MRTs at short intervals were not, we propose that two different mechanisms are involved in the decreasing of MRTs: warning and temporal expectancy. Our data support the hypothesis that the temporal component involved with the preparatory stages for motor responses can be shared by saccadic movements and key press responses, allowing the reduction on motor latencies after the visual offset in the gap paradigm. Our data corroborate the three components model for the gap effect. In our view, the question of the existence or not of a gap effect for manual responses is essentially conceptual.