Psychophysiology
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To investigate whether facial expression is processed in the absence of conscious awareness, ERPs were recorded in a task in which participants had to identify the expression of masked fearful and neutral target faces. On supraliminal trials (200 ms target duration), in which identification performance was high, a sustained positivity to fearful versus neutral target faces started 140 ms after target face onset. On subliminal trials (8 ms target duration), identification performance was at chance level, but ERPs still showed systematic fear-specific effects. ⋯ A subsequent enhanced N2 to fearful faces was only present for subliminal trials. In contrast, a P3 enhancement to fearful faces was observed on supraliminal but not subliminal trials. Results demonstrate rapid emotional expression processing in the absence of awareness.
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Elevated neuroticism is associated with increased psychological reactivity to stressors. Research on individual differences and physiological reactivity (e.g., electrodermal activity), however, has focused on clinical samples and measures of basal activity (e.g., nonspecific skin conductance responses) or responses to nonaffective stimuli. ⋯ Individuals higher in neuroticism exhibited both greater skin conductance reactivity to emotional (and particularly aversive) pictures as well as more extended reactivity than did emotionally stable individuals. Implications for health are discussed.
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Emotional facial expressions have affective significance. Smiles, for example, are perceived as positive and responded to with increased happiness, whereas angry expressions are perceived as negative and threatening. Yet, these perceptions are modulated in part by facial morphological cues related to the sex of the expresser. ⋯ For this 14 male and 16 female undergraduates saw happy, neutral, and angry facial expressions as well as positive and negative pictures. The postauricular reflex was potentiated during happy expressions and inhibited during anger expressions; however, as expected, this pattern was more clearly found for female expressers. Conversely, the expected pattern of eyeblink startle potentiation during angry faces and inhibition during happy faces was found only for male expressers.
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The present study explored fear acquisition in differential delay versus trace conditioning in regard to the potential role of the acquired contingency awareness. One of two neutral pictures (CS+) either coterminated with (delay group; n=32) or was followed by the aversive unconditioned stimulus (UCS) after CS offset (trace group; n=32), while startle blink and skin conductance responses (SCR) were measured. ⋯ SCR conditioning was generally only obtained for aware participants. The present results suggest a more implicit learning process in delay fear conditioning, whereas the explicit acquisition of contingency awareness might be a prerequisite for trace fear conditioning.
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Brain-computer interfaces (BCI) allow control of computers or external devices with regulation of brain activity alone. Invasive BCIs, almost exclusively investigated in animal models using implanted electrodes in brain tissue, and noninvasive BCIs using electrophysiological recordings in humans are described. Clinical applications were reserved with few exceptions for the noninvasive approach: communication with the completely paralyzed and locked-in syndrome with slow cortical potentials, sensorimotor rhythm and P300, and restoration of movement and cortical reorganization in high spinal cord lesions and chronic stroke. ⋯ At present no firm conclusion about the clinical utility of BCI for the control of voluntary movement can be made. Invasive multielectrode BCIs in otherwise healthy animals allowed execution of reaching, grasping, and force variations based on spike patterns and extracellular field potentials. The newly developed fMRI-BCIs and NIRS-BCIs, like EEG BCIs, offer promise for the learned regulation of emotional disorders and also disorders of young children.