Traditional theories of moral psychology emphasize reasoning and "higher cognition," while more recent work emphasizes the role of emotion. The present fMRI data support a theory of moral judgment according to which both "cognitive" and emotional processes play crucial and sometimes mutually competitive roles. The present results indicate that brain regions associated with abstract reasoning and cognitive control (including dorsolateral prefrontal cortex and anterior cingulate cortex) are recruited to resolve difficult personal moral dilemmas in which utilitarian values require "personal" moral violations, violations that have previously been associated with increased activity in emotion-related brain regions. Several regions of frontal and parietal cortex predict intertrial differences in moral judgment behavior, exhibiting greater activity for utilitarian judgments. We speculate that the controversy surrounding utilitarian moral philosophy reflects an underlying tension between competing subsystems in the brain.
Deciding whether an unfamiliar person is trustworthy is one of the most important decisions in social environments. We used functional magnetic resonance imaging to show that the amygdala is involved in implicit evaluations of trustworthiness of faces, consistent with prior findings. The amygdala response increased as perceived trustworthiness decreased in a task that did not demand person evaluation. More importantly, we tested whether this response is due to an individual's idiosyncratic perception or to face properties that are perceived as untrustworthy across individuals. The amygdala response was better predicted by consensus ratings of trustworthiness than by an individual's own judgments. Individual judgments accounted for little residual variance in the amygdala after controlling for the shared variance with consensus ratings. These findings suggest that the amygdala automatically categorizes faces according to face properties commonly perceived to signal untrustworthiness.
Previous research on the superior temporal sulcus (STS) has shown that it responds more to facial expressions than to neutral faces. Here, we extend our understanding of the STS in two ways. First, using targeted high-resolution fMRI measurements of the lateral cortex and multivoxel pattern analysis, we show that the response to seven categories of dynamic facial expressions can be decoded in both the posterior STS (pSTS) and anterior STS (aSTS). We were also able to decode patterns corresponding to these expressions in the frontal operculum (FO), a structure that has also been shown to respond to facial expressions. Second, we measured the similarity structure of these representations and found that the similarity structure in the pSTS significantly correlated with the perceptual similarity structure of the expressions. This was the case regardless of whether we used pattern classification or more traditional correlation techniques to extract the neural similarity structure. These results suggest that distributed representations in the pSTS could underlie the perception of facial expressions.
The perception of faces evokes characteristic electrophysiological responses at discrete loci in human fusiform gyrus and adjacent ventral occipitotemporal cortical sites. Prominent among these responses are a surface-negative potential at ∼200-ms postonset (face-N200) and face-induced spectral perturbations in the gamma band (face-γERSP). The degree to which these responses represent activity in the same cortical loci and the degree to which they are influenced by the same perceptual and task variables are unknown. We evaluated this anatomical colocalization and functional correlation in 2 experiments in which the electrocorticogram was recorded from subdural electrodes in 51 participants. Experiment 1 investigated the category specificity of the γERSP and its colocalization with the face-N200. Experiment 2 examined differences in face-N200 and face-γERSP to face stimuli that varied in featural complexity. We found that γERSP is a category-specific phenomenon with separate, though overlapping, category sensitivities as the N200. Further, the presence of face-γERSP at an electrode site significantly predicted the presence and amplitude of face-N200 at that site. However, the converse was not true in that face-N200 was evoked by impoverished face stimuli that did not induce face-γERSP. These results demonstrate that these electrophysiological responses reflect separate components of the brain's face processing system.
The amygdala is involved in the evaluation of novel stimuli, including faces. We examined whether the amygdala is engaged during the evaluation of emotionally neutral faces along trait-specific dimensions such as trustworthiness and attractiveness or along a general valence dimension. Using behavioral data from evaluation of faces on 14 trait dimensions and fMRI data from an implicit evaluation paradigm, we show that the extent to which the amygdala responds to variations of faces on specific dimensions is a function of the valence content of these dimensions. Variations on dimensions with clear valence connotations (e.g. trustworthiness) engaged the amygdala more strongly than variations on dimensions with less clear valence connotations (e.g. dominance). In addition to the amygdala, several other regions--right superior occipital gyrus, right middle temporal/occipital gyrus and bilateral fusiform gyri--were involved in valence evaluation of faces. However, the relation between these regions and face valence was accounted for by the amygdala's response to faces. The findings suggest that the amygdala (i) automatically evaluates novel faces along a general valence dimension; and (ii) modulates a face responsive network of regions in occipital and temporal cortices.
Autism spectrum disorders (ASDs) are typically characterized by impaired social interaction and communication, narrow interests, and repetitive behaviors. The heterogeneity in the severity of these characteristics across individuals with ASD has led some researchers to suggest that these disorders form a continuum which extends into the general, or “typical,” population, and there is growing evidence that the extent to which typical adults display autistic traits, as measured using the autism-spectrum quotient (AQ), predicts performance on behavioral tasks that are impaired in ASD. Here, we show that variation in autism spectrum traits is related to cortical structure and function within the typical population. Voxel-based morphometry showed that increased AQ scores were associated with decreased white matter volume in the posterior superior temporal sulcus (pSTS), a region important in processing socially relevant stimuli and associated with structural and functional impairments in ASD. In addition, AQ was correlated with the extent of cortical deactivation of an adjacent area of pSTS during a Stroop task relative to rest, reflecting variation in resting state function. The results provide evidence that autism spectrum characteristics are reflected in neural structure and function across the typical (non-ASD) population.
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