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Abstract Research in affective science includes over one hundred thousand articles, the vast majority of which have been published in only the past two decades. The size and rapid growth of this field have led to unique challenges for the twenty-first-century scientist including how to develop both breadth and depth of scholarship, curb siloing and promote integrative and interdisciplinary framework, and represent and monitor the field in its entirety. Here, we help address these issues by compactly mapping out this enormous field using citation network analysis (CNA). We generated a citation matrix of over 100,000 publications and over 1 million citations since the seminal works on emotion by Charles Darwin (1872) and William James (1884). Using graph theory metric and content analysis of titles and abstracts, we identified and characterized the contents of 69 research communities, their most influential articles, and their interconnectedness with each other. We further identified potential “missed connections” between communities that share similar content but do not have strong citation-based connections. In doing so, we establish the first, low-dimensional representation, or field-wide map, of a substantial portion of the affective sciences literature. This panoramic view of the field provides affective and non-affective scientists alike with the means to rapidly survey dozens of major research communities and topics in the field, guide scholarship development, and identify gaps and connections for developing an integrative science. 

Affective abstraction refers to how people conceptualize affective states in terms of category-level re- presentations that generalize across speci!c situations (e.g., “fear” as evoked by heights, predators, and haunted houses). Here, we develop a novel task for assessing affective abstraction and test its relations with trait alexithymia, depression, and autism spectrum quotient. In a preregistered online study, participants completed a set of tasks in which they matched a cue image with one of two probe images based on similarity of affective experience. In a discrete emotion version of the task, the cue and target probe matched on a discrete emotion category while controlling for valence. In a valence version of the task, the cue and target probe matched on valence (i.e., pleasantness or unpleasantness). We further varied the degree of abstraction such that some judgments crossed semantic categories (e.g., a house cue with animal probes). Accuracy, as indexed by the proportion of choices that accorded with norms, predicted trait measures of alexithymia, depression, and autism quotient with medium effect sizes. We conducted an integrative data analysis by including data from three other (nonpreregistered) samples (N = 435) and found substantial moderation by sampling population (Amazon Mechanical Turk, college students) and partial moderation by gender identity. Additional constraints on generalization include that our sample included predominantly White American adults between the ages of 23 and 64. These results provide preliminary support for the notion that affective abstraction may re"ect a transdiagnostic psychological process of broad relevance to individual differences in affective processing. 

Abstract Although emotion words such as “anger,” “disgust,” “happiness,” or “pride” are often thought of as mere labels, increasing evidence points to language as being important for emotion perception and experience. Emotion words may be particularly important for facilitating access to the emotion concepts. Indeed, deficits in semantic processing or impaired access to emotion words interfere with emotion perception. Yet, it is unclear what these behavioral findings mean for affective neuroscience. Thus, we examined the brain areas that support processing of emotion words using representational similarity analysis of functional magnetic resonance imaging data (N = 25). In the task, participants saw 10 emotion words (e.g. “anger,” “happiness”) while in the scanner. Participants rated each word based on its valence on a continuous scale ranging from 0 (Pleasant/Good) to 1 (Unpleasant/Bad) scale to ensure they were processing the words. Our results revealed that a diverse range of brain areas including prefrontal, midline cortical, and sensorimotor regions contained information about emotion words. Notably, our results overlapped with many regions implicated in decoding emotion experience by prior studies. Our results raise questions about what processes are being supported by these regions during emotion experience. 

The periaqueductal gray (PAG) is a small midbrain structure that surrounds the cerebral aqueduct, regulates brain–body communication, and is often studied for its role in “fight-or-flight” and “freezing” responses to threat. We used ultra-high-field 7 T fMRI to resolve the PAG in humans and distinguish it from the cerebral aqueduct, examining its in vivo function during a working memory task (N = 87). Both mild and moderate cognitive demands elicited spatially similar patterns of whole-brain blood oxygenation level-dependent (BOLD) response, and moderate cognitive demand elicited widespread BOLD increases above baseline in the brainstem. Notably, these brainstem increases were not significantly greater than those in the mild demand condition, suggesting that a subthreshold brainstem BOLD increase occurred for mild cognitive demand as well. Subject-specific masks were group aligned to examine PAG response. In PAG, both mild and moderate demands elicited a well-defined response in ventrolateral PAG, a region thought to be functionally related to anticipated painful threat in humans and nonhuman animals—yet, the present task posed only the most minimal (if any) “threat,” with the cognitive tasks used being approximately as challenging as remembering a phone number. These findings suggest that the PAG may play a more general role in visceromotor regulation, even in the absence of threat. 

Abstract Traditionally, lust and pride have been considered pleasurable, yet sinful in the West. Conversely, guilt is often considered aversive, yet valuable. These emotions illustrate how evaluations about specific emotions and beliefs about their hedonic properties may often diverge. Evaluations about specific emotions may shape important aspects of emotional life (e.g. in emotion regulation, emotion experience and acquisition of emotion concepts). Yet these evaluations are often understudied in affective neuroscience. Prior work in emotion regulation, affective experience, evaluation/attitudes and decision-making point to anterior prefrontal areas as candidates for supporting evaluative emotion knowledge. Thus, we examined the brain areas associated with evaluative and hedonic emotion knowledge, with a focus on the anterior prefrontal cortex. Participants (N = 25) made evaluative and hedonic ratings about emotion knowledge during functional magnetic resonance imaging (fMRI). We found that greater activity in the medial prefrontal cortex (mPFC), ventromedial PFC (vmPFC) and precuneus was associated with an evaluative (vs hedonic) focus on emotion knowledge. Our results suggest that the mPFC and vmPFC, in particular, may play a role in evaluating discrete emotions. 

Degeneracy in biological systems refers to a many-to-one mapping between physical structures and their functional (including psychological) outcomes. Despite the ubiquity of the phenomenon, traditional analytical tools for modeling degeneracy in neuroscience are extremely limited. In this study, we generated synthetic datasets to describe three situations of degeneracy in fMRI data to demonstrate the limitations of the current univariate approach. We describe a novel computational approach for the analysis referred to as neural topographic factor analysis (NTFA). NTFA is designed to capture variations in neural activity across task conditions and participants. The advantage of this discovery-oriented approach is to reveal whether and how experimental trials and participants cluster into task conditions and participant groups. We applied NTFA on simulated data, revealing the appropriate degeneracy assumption in all three situations and demonstrating NTFA’s utility in uncovering degeneracy. Lastly, we discussed the importance of testing degeneracy in fMRI data and the implications of applying NTFA to do so.