{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,17]],"date-time":"2026-05-17T10:20:43Z","timestamp":1779013243298,"version":"3.51.4"},"reference-count":46,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,1,12]],"date-time":"2026-01-12T00:00:00Z","timestamp":1768176000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Hum. Neurosci."],"abstract":"<jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>Understanding how emotions are encoded at the neural level remains a central challenge in human neuroscience. Facial expressions are among the most powerful and frequently used stimuli to study emotion processing. Face perception itself is a complex function supported by a core network\u2014including bilateral occipito-fusiform and superior temporal regions\u2014and an extended network involving anterior structures such as the bilateral amygdalae. However, previous findings on how emotional content modulates these networks have been inconsistent.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>To disentangle perceptual and affective components of face emotion processing, we combined high-frequency pupillometry with functional magnetic resonance imaging (fMRI). Pupillary dilation serves as a sensitive index of two distinct processes: perceptual load, reflecting the informational complexity of a face, and arousal, indicating its immediate sensory impact. In our study, 25 participants (13 female) viewed faces expressing anger, fear, happiness, or neutrality as well as luminance-matched houses serving as control stimuli. A one-back task unrelated to emotion masked the true experimental purpose.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Relative to houses, faces elicited stronger pupillary dilations as well as enhanced blood-oxygen-level-dependent (BOLD) activity in bilateral occipital and fusiform cortices as well as in both amygdalae. Among facial expressions, angry faces evoked the largest pupillary dilations, while fearful faces elicited the strongest neural responses within a right-lateralized network centered on the superior temporal sulcus (rSTS). Across all faces&amp;gt;houses (conjunction minimum-statistic inference), pupil size correlated positively with BOLD activity in the right fusiform gyrus (rFFG), left inferior occipital gyrus (lIOG), bilateral calcarine cortex, and bilateral lingual gyrus.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>These findings indicate that emotional faces impose a higher perceptual load than matched control stimuli, engaging a distributed network spanning early visual and attention-related areas. In conclusion, our results suggest that emotional quality is specified early in the perceptual process, with divergent pupillary and neural signatures separating arousal-driven threat responses (anger) from socially complex alarm cues (fear).<\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fnhum.2025.1739802","type":"journal-article","created":{"date-parts":[[2026,1,12]],"date-time":"2026-01-12T08:17:54Z","timestamp":1768205874000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["Differential arousal and neural engagement for angry and fearful faces: a combined pupillometric and fMRI study"],"prefix":"10.3389","volume":"19","author":[{"given":"Kim C.","family":"Wende","sequence":"first","affiliation":[{"name":"Department of Psychiatry and Psychotherapy, University of Marburg","place":["Marburg, Germany"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roman","family":"Kessler","sequence":"additional","affiliation":[{"name":"Department of Psychiatry and Psychotherapy, University of Marburg","place":["Marburg, Germany"]},{"name":"Institute of Child and Adolescent Psychiatry, University of Kiel","place":["Kiel, Germany"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kristin M.","family":"Rusch","sequence":"additional","affiliation":[{"name":"Department of Psychiatry and Psychotherapy, University of Marburg","place":["Marburg, Germany"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jens","family":"Sommer","sequence":"additional","affiliation":[{"name":"Department of Psychiatry and Psychotherapy, University of Marburg","place":["Marburg, Germany"]},{"name":"Core-Facility Brainimaging, Faculty of Medicine, University of Marburg","place":["Marburg, Germany"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andreas","family":"Jansen","sequence":"additional","affiliation":[{"name":"Department of Psychiatry and Psychotherapy, University of Marburg","place":["Marburg, Germany"]},{"name":"Core-Facility Brainimaging, Faculty of Medicine, University of Marburg","place":["Marburg, Germany"]}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1965","published-online":{"date-parts":[[2026,1,12]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","first-page":"22959","DOI":"10.1038\/srep22959","article-title":"Brain mechanisms associated with internally directed attention and self-generated thought","volume":"6","author":"Benedek","year":"2016","journal-title":"Sci. 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