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One important aspect of metacognition is the ability to accurately evaluate one's performance. People vary widely in their metacognitive ability and in general are too confident when evaluating their performance. This often leads to poor... more
One important aspect of metacognition is the ability to accurately evaluate one's performance. People vary widely in their metacognitive ability and in general are too confident when evaluating their performance. This often leads to poor decision making with potentially disastrous consequences. To further our understanding of the neural underpinnings of these processes, this fMRI study investigated inter-individual differences in metacognitive ability and effects of trial-by-trial variation in subjective feelings of confidence when making metacognitive assessments. Participants (N ¼ 308) evaluated their performance in a high-level social and cognitive reasoning task. The results showed that higher metacognitive accuracy was associated with a decrease in activation in the anterior medial prefrontal cortex, an area previously linked to metacog-nition on perception and memory. Moreover, the feeling of confidence about one's choices was associated with an increase of activation in reward, memory and motor related areas including bilateral striatum and hippocampus, while less confidence was associated with activation in areas linked with negative affect and uncertainty, including dorsomedial prefrontal and bilateral orbitofrontal cortex. This might indicate that positive affect is related to higher confidence thereby biasing metacognitive decisions towards overconfidence. In support, behavioural analyses revealed that increased confidence was associated with lower metacognitive accuracy.
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Most instances of social interaction provide a wealth of information about the states of other people, be it sensations, feelings, thoughts, or convictions. How we represent these states has been a major question in social neuroscience,... more
Most instances of social interaction provide a wealth of information about the states of other people, be it sensations, feelings, thoughts, or convictions. How we represent these states has been a major question in social neuroscience, leading to the identification of two routes to understanding others: an affective route for the direct sharing of others' emotions (empathy) that involves, among others, anterior insula and middle anterior cingulate cortex and a cognitive route for representing and reasoning about others' states (Theory of Mind) that entails, among others, ventral temporoparietal junction and anterior and posterior midline regions. Additionally, research has revealed a number of situational and personal factors that shape the functioning of empathy and Theory of Mind. Concerning situational modulators, it has been shown, for instance, that ingroup membership enhances empathic responding and that Theory of Mind performance seems to be susceptible to stress. Personal modulators include psychopathological conditions, for which alterations in empathy and mentalizing have consistently been demonstrated; people on the autism spectrum, for instance, are impaired specifically in mentalizing, while spontaneous empathic responding seems selectively reduced in psychopathy. Given the multifaceted evidence for separability of the two routes, current research endeavors aiming at fostering interpersonal cooperation explore the differential malleability of affective and cognitive understanding of others.
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Observing eye contact between others enhances the tendency to subsequently follow their gaze and has been suggested to function as a social signal that adds meaning to an upcoming action or event. The present study investigated effects of... more
Observing eye contact between others enhances the tendency to subsequently follow their gaze and has been suggested to function as a social signal that adds meaning to an upcoming action or event. The present study investigated effects of observed eye contact in high-functioning autism (HFA). Two faces on a screen either looked at or away from each other before providing congruent or incongruent gaze cues to one of two target locations. In contrast to control participants, HFA participants did not depict enhanced gaze following after observing eye contact. Individuals with autism, hence, do not seem to process observed mutual gaze as a social signal indicating the relevance of upcoming (gaze) behaviour. This may be based on the reduced tendency of individuals with HFA to engage in social gaze behavior themselves, and might underlie some of the characteristic deficiencies in social communicative behaviour in autism.
Direct eye contact and motion onset are two powerful cues that capture attention. In the present study, we combined direct gaze with the sudden onset of motion to determine whether these cues have independent or shared influences.... more
Direct eye contact and motion onset are two powerful cues that capture attention. In the present study, we combined
direct gaze with the sudden onset of motion to determine whether these cues have independent or shared influences.
Participants identified targets presented randomly on one of four faces. Initially, two faces depicted direct gaze, and
two faces depicted averted gaze. Simultaneously with or 900 ms before target presentation, one face with averted gaze
switched to direct gaze, and one face with direct gaze switched to averted gaze. When gaze transitions and target
presentation were simultaneous, the greatest response-time facilitation occurred at the location of the sudden onset
of direct gaze. When target presentation was delayed, direct-gaze cues maintained a facilitatory influence, whereas
motion cues induced an inhibitory influence. These findings reveal that gaze cues and motion cues at the same location
influence information processing via independent and concurrently acting social and nonsocial attention channels.