Feng W, Luo W, Liao Y, Wang N, Gan T, Luo Y.
Brain Research, in press
Previous studies have shown differential event-related potentials (ERPs) to intensities of fearful facial expressions. There are indications that the eyes may be particularly relevant for the recognition of fearful expressions, even the amount of white sclera exposed above and on sides of the dark pupil could activate the amygdala response. To investigate whether the ERP differences between intensities of fearful expressions are driven by the differential salience of the eyes in the fearful faces, ERPs were measured within a backward masking paradigm, where observers were asked to do a gender decision task with male and female neutral faces. The emotional stimuli used were low-intensity (50%), prototypical (100%), and caricatured (150%) fearful eye whites that were derived from corresponding intensities of fearful faces respectively. Three groups of white squares that have the same pixels as the eye whites were created as control conditions. Analysis of the ERP data showed a linear increase in amplitudes of the parietal-occipital P120 by three intensities of fearful eye whites. These ERP effects were proved sensitive to intensities of negative emotions but not to the simple physical features as the same patterns of differences were not observed on white squares. Larger parietal-occipital P250 amplitudes were observed for caricatured 150% than low-intensity 50% fearful eye-white. It might reflect the subcortical pathway of emotion-specific, fearful processing. The results demonstrate that the human brain is sensitive to intensities of fear, even if just shown intensities of fearful eye-white in the absence of awareness.
Monday, July 06, 2009
ARTICLE UPDATE - Human brain responsivity to masked different intensities of fearful eye whites: An ERP study.
ARTICLE UPDATE - Genetics of Emotion Regulation.
Canli T, Ferri J, Duman EA.
Neuroscience, in press
Emotions can be powerful drivers of behavior that may be adaptive or maladaptive for the individual. Thus, the ability to alter one's emotions, to regulate them, should be beneficial to an individual's success of survival and fitness. What is the biological basis of this ability? And what are the biological mechanisms that impart individual differences in the ability to regulate emotion? In this article, we will first introduce readers to the construct of emotion regulation, and the various strategies that individuals may utilize to regulate their emotions. We will then point to evidence that suggests genetic contributions (alongside environmental contributions) to individual differences in emotion regulation. To date, efforts to identify specific genetic mechanisms involved in emotion regulation have focused on common gene variants (i.e., variants that exist in > 1% of the population, referred to as polymorphisms) and their association with specific emotion regulation strategies or the neural substrate mediating these strategies. We will discuss these efforts, and conclude with a call to expand the set of experimental paradigms and putative molecular mechanisms, in order to significantly advance our understanding of the molecular mechanisms by which genes are involved in emotion regulation.
Neuroscience, in press
Emotions can be powerful drivers of behavior that may be adaptive or maladaptive for the individual. Thus, the ability to alter one's emotions, to regulate them, should be beneficial to an individual's success of survival and fitness. What is the biological basis of this ability? And what are the biological mechanisms that impart individual differences in the ability to regulate emotion? In this article, we will first introduce readers to the construct of emotion regulation, and the various strategies that individuals may utilize to regulate their emotions. We will then point to evidence that suggests genetic contributions (alongside environmental contributions) to individual differences in emotion regulation. To date, efforts to identify specific genetic mechanisms involved in emotion regulation have focused on common gene variants (i.e., variants that exist in > 1% of the population, referred to as polymorphisms) and their association with specific emotion regulation strategies or the neural substrate mediating these strategies. We will discuss these efforts, and conclude with a call to expand the set of experimental paradigms and putative molecular mechanisms, in order to significantly advance our understanding of the molecular mechanisms by which genes are involved in emotion regulation.
Saturday, June 27, 2009
ARTICLE UPDATE - Mirror of the soul: a cortical stimulation study on recognition of facial emotions.
Giussani C, Pirillo D, Roux FE.
Journal of Neurosurgery, in press
Object The capability of recognizing the expressions of facial emotions has been hypothesized to depend on a right hemispheric cortical-subcortical network. Its impairment deeply disturbs social relationships. To spare right hemispheric cortical areas involved in recognizing facial emotion, the authors used intraoperative cortical stimulation and the awake surgery technique in a consecutive series of patients. The feasibility and the interest to map them during brain mapping for neurosurgical procedures are discussed. Methods After a preoperative neuropsychological evaluation, 18 consecutive patients with right hemispheric lesions (5 metastases, 6 high-grade gliomas, 4 low-grade gliomas, 2 arteriovenous malformations, and 1 malignant meningioma) were tested by intraoperative cortical stimulation while performing a facial emotion recognition task along with sensorimotor and visuospatial tasks. Results Three hundred eighty-six cortical sites were studied. Five (1.30%) reproducible interference sites for facial emotion recognition were identified in 5 patients: 1 site in the medial segment of T1; 1 site in the posterior segment of T1; 1 site in the posterior segment of T2; and 2 sites in the supramarginal gyrus. No selective impairment was found regarding the emotion category. All facial emotion recognition sites were spared during surgery, and none of the patients experienced postoperative deficits in recognition of facial emotions. Conclusions The finding of interference sites in facial emotion recognition in the right posterior perisylvian area, independent to sensorimotor or visuospatial orientation processes, reinforces the theory about the role of anatomically and functionally segregated right hemisphere structures in this cognitive process. The authors advocate offering a brain mapping of facial emotion recognition to patients with right posterior perisylvian tumors.
Journal of Neurosurgery, in press
Object The capability of recognizing the expressions of facial emotions has been hypothesized to depend on a right hemispheric cortical-subcortical network. Its impairment deeply disturbs social relationships. To spare right hemispheric cortical areas involved in recognizing facial emotion, the authors used intraoperative cortical stimulation and the awake surgery technique in a consecutive series of patients. The feasibility and the interest to map them during brain mapping for neurosurgical procedures are discussed. Methods After a preoperative neuropsychological evaluation, 18 consecutive patients with right hemispheric lesions (5 metastases, 6 high-grade gliomas, 4 low-grade gliomas, 2 arteriovenous malformations, and 1 malignant meningioma) were tested by intraoperative cortical stimulation while performing a facial emotion recognition task along with sensorimotor and visuospatial tasks. Results Three hundred eighty-six cortical sites were studied. Five (1.30%) reproducible interference sites for facial emotion recognition were identified in 5 patients: 1 site in the medial segment of T1; 1 site in the posterior segment of T1; 1 site in the posterior segment of T2; and 2 sites in the supramarginal gyrus. No selective impairment was found regarding the emotion category. All facial emotion recognition sites were spared during surgery, and none of the patients experienced postoperative deficits in recognition of facial emotions. Conclusions The finding of interference sites in facial emotion recognition in the right posterior perisylvian area, independent to sensorimotor or visuospatial orientation processes, reinforces the theory about the role of anatomically and functionally segregated right hemisphere structures in this cognitive process. The authors advocate offering a brain mapping of facial emotion recognition to patients with right posterior perisylvian tumors.
ARTICLE UPDATE - Influence of attention to somatic information on emotional and autonomic responses.
Murakami H, Ohira H, Matsunaga M, Kimura K.
Perceptual Motor Skills, 108, 531-539
The present study aimed to investigate the dissociable effects of two forms of self-focus on emotional and autonomic responses. One form is suppression, which includes the suppression of heart rate and self-evaluation of performance. The other is observation, which includes attention to one's own heart rate with no suppression and no evaluation. 26 undergraduate and graduate students from the Nagoya University campus (13 men, 13 women), ages 18 to 24 years (M = 20.7, SD = 1.6) were recruited. Participants were provided with their own heart rate as feedback for 5 min., during which participants conducted a self-focus manipulation. Several days after the experimental session for one condition, the same participants conducted another experimental session for the other condition. Instruction to suppress enhanced physiological arousal and subsequent negative emotions; however, instruction to observe did not increase physiological arousal or negative emotions.
Perceptual Motor Skills, 108, 531-539
The present study aimed to investigate the dissociable effects of two forms of self-focus on emotional and autonomic responses. One form is suppression, which includes the suppression of heart rate and self-evaluation of performance. The other is observation, which includes attention to one's own heart rate with no suppression and no evaluation. 26 undergraduate and graduate students from the Nagoya University campus (13 men, 13 women), ages 18 to 24 years (M = 20.7, SD = 1.6) were recruited. Participants were provided with their own heart rate as feedback for 5 min., during which participants conducted a self-focus manipulation. Several days after the experimental session for one condition, the same participants conducted another experimental session for the other condition. Instruction to suppress enhanced physiological arousal and subsequent negative emotions; however, instruction to observe did not increase physiological arousal or negative emotions.
ARTICLE UPDATE - Worry tendencies predict brain activation during aversive imagery.
Schienle A, Schäfer A, Pignanelli R, Vaitl D.
Neuroscience Letters, in press
Because of its abstract nature, worrying might function as an avoidance response in order to cognitively disengage from fearful imagery. The present functional magnetic resonance imaging study investigated neural correlates of aversive imagery and their association with worry tendencies, as measured by the Penn State Worry Questionnaire (PSWQ). Nineteen healthy women first viewed, and subsequently imagined pictures from two categories, 'threat' and 'happiness'. Worry tendencies were negatively correlated with brain activation in the anterior cingulate cortex, the prefrontal cortex (dorsolateral, dorsomedial, ventrolateral), the parietal cortex and the insula. These negative correlations between PSWQ scores and localized brain activation were specific for aversive imagery. Moreover, activation in the abovementioned regions was positively associated with the experienced vividness of both pleasant and unpleasant mental pictures. As the identified brain regions are involved in emotion regulation, vivid imagery and memory retrieval, a lowered activity in high PSWQ scorers might be associated with cognitive disengagement from aversive imagery as well as insufficient refresh rates of mental pictures. Our preliminary findings encourage future imagery studies on generalized anxiety disorder patients, as one of the main symptoms of this disorder is excessive worrying.
Neuroscience Letters, in press
Because of its abstract nature, worrying might function as an avoidance response in order to cognitively disengage from fearful imagery. The present functional magnetic resonance imaging study investigated neural correlates of aversive imagery and their association with worry tendencies, as measured by the Penn State Worry Questionnaire (PSWQ). Nineteen healthy women first viewed, and subsequently imagined pictures from two categories, 'threat' and 'happiness'. Worry tendencies were negatively correlated with brain activation in the anterior cingulate cortex, the prefrontal cortex (dorsolateral, dorsomedial, ventrolateral), the parietal cortex and the insula. These negative correlations between PSWQ scores and localized brain activation were specific for aversive imagery. Moreover, activation in the abovementioned regions was positively associated with the experienced vividness of both pleasant and unpleasant mental pictures. As the identified brain regions are involved in emotion regulation, vivid imagery and memory retrieval, a lowered activity in high PSWQ scorers might be associated with cognitive disengagement from aversive imagery as well as insufficient refresh rates of mental pictures. Our preliminary findings encourage future imagery studies on generalized anxiety disorder patients, as one of the main symptoms of this disorder is excessive worrying.
Friday, June 19, 2009
ARTICLE UPDATE - In search of specificity: functional MRI in the study of emotional experience.
Schienle A, Schäfer A.
International Journal of Psychophysiology, 73, 22-26.
The growing availability of functional magnetic resonance imaging (fMRI) with its property of high spatial resolution has energized the search for specific neural substrates of basic emotions and their feeling components. In the present article, we address the question as to whether recent fMRI studies on primary affective experiences have truly helped to pinpoint emotion-specific areas in the human brain or whether these studies are afflicted with methodological problems which make such inferences difficult. As one approach for improvement, we suggest the combination of fMRI with methods characterized by high temporal resolution, such as electroencephalography (EEG). Simultaneous recoding allows the correlation of temporally specific EEG components (e.g., the late positive potential) with regional blood-oxygen-level-dependent (BOLD) signals during affective experiences. Combined information on the source as well as the exact temporal pattern of a neural affective response will help to improve our understanding of emotion-specific brain activation.
International Journal of Psychophysiology, 73, 22-26.
The growing availability of functional magnetic resonance imaging (fMRI) with its property of high spatial resolution has energized the search for specific neural substrates of basic emotions and their feeling components. In the present article, we address the question as to whether recent fMRI studies on primary affective experiences have truly helped to pinpoint emotion-specific areas in the human brain or whether these studies are afflicted with methodological problems which make such inferences difficult. As one approach for improvement, we suggest the combination of fMRI with methods characterized by high temporal resolution, such as electroencephalography (EEG). Simultaneous recoding allows the correlation of temporally specific EEG components (e.g., the late positive potential) with regional blood-oxygen-level-dependent (BOLD) signals during affective experiences. Combined information on the source as well as the exact temporal pattern of a neural affective response will help to improve our understanding of emotion-specific brain activation.
Saturday, June 13, 2009
ARTICLE UPDATE - Emotions in motion: Dynamic compared to static facial expressions of disgust and happiness reveal more widespread emotion-specific ac
Emotions in motion: Dynamic compared to static facial expressions of disgust and happiness reveal more widespread emotion-specific activations.
Brain Research, in press
In social contexts, facial expressions are dynamic in nature and vary rapidly in relation to situational requirements. However, there are very few fMRI studies using dynamic emotional stimuli. The aim of this study was (1) to introduce and evaluate a new stimulus database of static and dynamic emotional facial expressions according to arousal and recognizability investigated by a rating by both participants of the present fMRI study and by an external sample of 30 healthy women, (2) to examine the neural networks involved in emotion perception of static and dynamic facial stimuli separately, and (3) to examine the impact of motion on the emotional processing of dynamic compared to static face stimuli. A total of 16 females participated in the present fMRI study performing a passive emotion perception task including static and dynamic faces of neutral, happy and disgusted expressions. Comparing dynamic stimuli to static faces indicated enhanced emotion-specific brain activation patterns in the parahippocampal gyrus (PHG) including the amygdala (AMG), fusiform gyrus (FG), superior temporal gyrus (STG), inferior frontal gyrus (IFG), and occipital and orbitofrontal cortex (OFC). These regions have been discussed to be associated with emotional memory encoding, the perception of threat, facial identity, biological motion, the mirror neuron system, an increase of emotional arousal, and reward processing, respectively. Post hoc ratings of the dynamic stimuli revealed a better recognizability in comparison to the static stimuli. In conclusion, dynamic facial expressions might provide a more appropriate approach to examine the processing of emotional face perception than static stimuli.
Brain Research, in press
In social contexts, facial expressions are dynamic in nature and vary rapidly in relation to situational requirements. However, there are very few fMRI studies using dynamic emotional stimuli. The aim of this study was (1) to introduce and evaluate a new stimulus database of static and dynamic emotional facial expressions according to arousal and recognizability investigated by a rating by both participants of the present fMRI study and by an external sample of 30 healthy women, (2) to examine the neural networks involved in emotion perception of static and dynamic facial stimuli separately, and (3) to examine the impact of motion on the emotional processing of dynamic compared to static face stimuli. A total of 16 females participated in the present fMRI study performing a passive emotion perception task including static and dynamic faces of neutral, happy and disgusted expressions. Comparing dynamic stimuli to static faces indicated enhanced emotion-specific brain activation patterns in the parahippocampal gyrus (PHG) including the amygdala (AMG), fusiform gyrus (FG), superior temporal gyrus (STG), inferior frontal gyrus (IFG), and occipital and orbitofrontal cortex (OFC). These regions have been discussed to be associated with emotional memory encoding, the perception of threat, facial identity, biological motion, the mirror neuron system, an increase of emotional arousal, and reward processing, respectively. Post hoc ratings of the dynamic stimuli revealed a better recognizability in comparison to the static stimuli. In conclusion, dynamic facial expressions might provide a more appropriate approach to examine the processing of emotional face perception than static stimuli.
ARTICLE UPDATE - Emotion and space. Lateralized emotional word detection depends on line bisection bias.
Tamagni C, Mantei T, Brugger P.
Neuroscience, in press
There is converging evidence, from various independent areas of neuroscience, for a functional specialization of the left and right cerebral hemispheres for positive and negative emotions, respectively ("valence theory" of emotional processing). One subfield, however, has produced mixed results, i.e. work on the detection of parafoveally presented positively or negatively emotional words by healthy subjects. Right or left visual field advantages were described and interpreted as reflecting the superiority of either the left hemisphere (LH) for linguistic material, or of the right hemisphere (RH) for highly emotional stimuli. Here we show that 48 healthy, right-handed participants' performance on a lateralized lexical decision task depends on their individual inclination to bisect a line to the left or right of the objective center. Only those with a bisection bias to the right showed the LH advantage for word detection known from the neuropsychological literature. Negative emotional words were processed with comparable accuracy in the two visual fields. However, a recognition advantage for negative over positive emotional words was found exclusively for those participants with a leftward line bisection bias. These results suggest that in work on functional hemispheric differences state variables like stimulus lateralization and word emotionality may be less decisive than the trait variable of lateral hemispatial attention. We propose a cautious reconsideration of the concept of "hemisphericity", which once emphasized individual differences in baseline hemispheric arousal, but was later dismissed in a reaction to oversimplifications in popular science accounts.
Neuroscience, in press
There is converging evidence, from various independent areas of neuroscience, for a functional specialization of the left and right cerebral hemispheres for positive and negative emotions, respectively ("valence theory" of emotional processing). One subfield, however, has produced mixed results, i.e. work on the detection of parafoveally presented positively or negatively emotional words by healthy subjects. Right or left visual field advantages were described and interpreted as reflecting the superiority of either the left hemisphere (LH) for linguistic material, or of the right hemisphere (RH) for highly emotional stimuli. Here we show that 48 healthy, right-handed participants' performance on a lateralized lexical decision task depends on their individual inclination to bisect a line to the left or right of the objective center. Only those with a bisection bias to the right showed the LH advantage for word detection known from the neuropsychological literature. Negative emotional words were processed with comparable accuracy in the two visual fields. However, a recognition advantage for negative over positive emotional words was found exclusively for those participants with a leftward line bisection bias. These results suggest that in work on functional hemispheric differences state variables like stimulus lateralization and word emotionality may be less decisive than the trait variable of lateral hemispatial attention. We propose a cautious reconsideration of the concept of "hemisphericity", which once emphasized individual differences in baseline hemispheric arousal, but was later dismissed in a reaction to oversimplifications in popular science accounts.
ARTICLE UPDATE - EEG coherence in humans: relationship with success in recognizing emotions in the voice.
Kislova OO, Rusalova MN.
Neuroscience and Behavioral Physiology, in press
EEG recordings from two groups of subjects - with high and low levels of recognition of emotions from voices were made. Comparisons were performed of the numbers of pairs of leads with different levels of coherence in baseline conditions and on recognition of emotions in six standard frequency ranges and in individual bands with 1-Hz steps. Significant differences were seen between groups 1 and 2 both in baseline conditions and during recognition of emotions: in most cases, coherence was greater in subjects with poor recognition of emotions from voices.
Neuroscience and Behavioral Physiology, in press
EEG recordings from two groups of subjects - with high and low levels of recognition of emotions from voices were made. Comparisons were performed of the numbers of pairs of leads with different levels of coherence in baseline conditions and on recognition of emotions in six standard frequency ranges and in individual bands with 1-Hz steps. Significant differences were seen between groups 1 and 2 both in baseline conditions and during recognition of emotions: in most cases, coherence was greater in subjects with poor recognition of emotions from voices.
Saturday, June 06, 2009
ARTICLE UPDATE - Prolonged reduction of electrocortical activity predicts correct performance during rapid serial visual processing.
Keil A, Heim S.
Psychophysiology, in press
Abstract When two targets are shown in a rapid temporal stream of distractors, performance for the second target (T2) is typically reduced when presented between 200 and 500 ms after the first (T1). The present study used the steady-state visual evoked potential (ssVEP), a continuous index of electrocortical facilitation, to compare brain responses in trials with correct versus incorrect T2 responses. We found a reduction of the electrocortical response following T1 in trials with correct T2 identification. By contrast, incorrect T2 trials were characterized by enhanced electrocortical amplitude. Amplitude attenuation predictive of successful T2 report was sustained over time, suggesting a reduction of resources allocated to the distractor stream in correct trials. Across intertarget intervals, T2 performance was a linear function of the ssVEP amplitude reduction in correct trials, weighted by the stimulus onset asynchrony.
Psychophysiology, in press
Abstract When two targets are shown in a rapid temporal stream of distractors, performance for the second target (T2) is typically reduced when presented between 200 and 500 ms after the first (T1). The present study used the steady-state visual evoked potential (ssVEP), a continuous index of electrocortical facilitation, to compare brain responses in trials with correct versus incorrect T2 responses. We found a reduction of the electrocortical response following T1 in trials with correct T2 identification. By contrast, incorrect T2 trials were characterized by enhanced electrocortical amplitude. Amplitude attenuation predictive of successful T2 report was sustained over time, suggesting a reduction of resources allocated to the distractor stream in correct trials. Across intertarget intervals, T2 performance was a linear function of the ssVEP amplitude reduction in correct trials, weighted by the stimulus onset asynchrony.
Saturday, May 30, 2009
PUBLICATION - Affective learning enhances activity and functional connectivity in early visual cortex.
Damaraju E, Huang YM, Barrett LF, Pessoa L.
Neuropsychologia, in press
This study examined the impact of task-irrelevant affective information on early visual processing regions V1-V4. Fearful and neutral faces presented with rings of different colors were used as stimuli. During the conditioning phase, fearful faces presented with a certain ring color (e.g., black) were paired with mild electrical stimulation. Neutral faces shown with rings of that color, as well as fearful or neutral faces shown with another ring color (e.g., white), were never paired with shock. Our findings revealed that fearful faces evoked enhanced blood oxygen level dependent (BOLD) responses in V1 and V4 compared to neutral faces. Faces embedded in a color ring that was paired with shock (e.g., black) evoked greater BOLD responses in V1-V4 compared to a ring color that was never paired with shock (e.g., white). Finally, BOLD responses in early visual cortex were tightly interrelated (i.e., correlated) during an affectively potent context (i.e., ring color) but not during a neutral one, suggesting that increased functional integration was present with affective learning. Taken together, the results suggest that task-irrelevant affective information not only influences evoked responses in early, retinotopically organized visual cortex, but also determines the pattern of responses across early visual cortex.
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Neuropsychologia, in press
This study examined the impact of task-irrelevant affective information on early visual processing regions V1-V4. Fearful and neutral faces presented with rings of different colors were used as stimuli. During the conditioning phase, fearful faces presented with a certain ring color (e.g., black) were paired with mild electrical stimulation. Neutral faces shown with rings of that color, as well as fearful or neutral faces shown with another ring color (e.g., white), were never paired with shock. Our findings revealed that fearful faces evoked enhanced blood oxygen level dependent (BOLD) responses in V1 and V4 compared to neutral faces. Faces embedded in a color ring that was paired with shock (e.g., black) evoked greater BOLD responses in V1-V4 compared to a ring color that was never paired with shock (e.g., white). Finally, BOLD responses in early visual cortex were tightly interrelated (i.e., correlated) during an affectively potent context (i.e., ring color) but not during a neutral one, suggesting that increased functional integration was present with affective learning. Taken together, the results suggest that task-irrelevant affective information not only influences evoked responses in early, retinotopically organized visual cortex, but also determines the pattern of responses across early visual cortex.
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ARTICLE UPDATE - Embodiment of emotion concepts.
Niedenthal PM, Winkielman P, Mondillon L, Vermeulen N.
Journal of Personality and Social Psychology, 96, 1120-1136
Theories of embodied cognition hold that higher cognitive processes operate on perceptual symbols and that concept use involves partial reactivations of the sensory-motor states that occur during experience with the world. On this view, the processing of emotion knowledge involves a (partial) reexperience of an emotion, but only when access to the sensory basis of emotion knowledge is required by the task. In 2 experiments, participants judged emotional and neutral concepts corresponding to concrete objects (Experiment 1) and abstract states (Experiment 2) while facial electromyographic activity was recorded from the cheek, brow, eye, and nose regions. Results of both studies show embodiment of specific emotions in an emotion-focused but not a perceptual-focused processing task on the same words. A follow up in Experiment 3, which blocked selective facial expressions, suggests a causal, rather than simply a correlational, role for embodiment in emotion word processing. Experiment 4, using a property generation task, provided support for the conclusion that emotions embodied in conceptual tasks are context-dependent situated simulations rather than associated emotional reactions. Implications for theories of embodied simulation and for emotion theories are discussed.
Journal of Personality and Social Psychology, 96, 1120-1136
Theories of embodied cognition hold that higher cognitive processes operate on perceptual symbols and that concept use involves partial reactivations of the sensory-motor states that occur during experience with the world. On this view, the processing of emotion knowledge involves a (partial) reexperience of an emotion, but only when access to the sensory basis of emotion knowledge is required by the task. In 2 experiments, participants judged emotional and neutral concepts corresponding to concrete objects (Experiment 1) and abstract states (Experiment 2) while facial electromyographic activity was recorded from the cheek, brow, eye, and nose regions. Results of both studies show embodiment of specific emotions in an emotion-focused but not a perceptual-focused processing task on the same words. A follow up in Experiment 3, which blocked selective facial expressions, suggests a causal, rather than simply a correlational, role for embodiment in emotion word processing. Experiment 4, using a property generation task, provided support for the conclusion that emotions embodied in conceptual tasks are context-dependent situated simulations rather than associated emotional reactions. Implications for theories of embodied simulation and for emotion theories are discussed.
ARTICLE UPDATE - Early and late temporo-spatial effects of contextual interference during perception of facial affect.
Frühholz S, Fehr T, Herrmann M.
International Journal of Psychophysiology, in press
Contextual features during recognition of facial affect are assumed to modulate the temporal course of emotional face processing. Here, we simultaneously presented colored backgrounds during valence categorizations of facial expressions. Subjects incidentally learned to perceive negative, neutral and positive expressions within a specific colored context. Subsequently, subjects made fast valence judgments while presented with the same face-color-combinations as in the first run (congruent trials) or with different face-color-combinations (incongruent trials). Incongruent trials induced significantly increased response latencies and significantly decreased performance accuracy. Contextual incongruent information during processing of neutral expressions modulated the P1 and the early posterior negativity (EPN) both localized in occipito-temporal areas. Contextual congruent information during emotional face perception revealed an emotion-related modulation of the P1 for positive expressions and of the N170 and the EPN for negative expressions. Highest amplitude of the N170 was found for negative expressions in a negatively associated context and the N170 amplitude varied with the amount of overall negative information. Incongruent trials with negative expressions elicited a parietal negativity which was localized to superior parietal cortex and which most likely represents a posterior manifestation of the N450 as an indicator of conflict processing. A sustained activation of the late LPP over parietal cortex for all incongruent trials might reflect enhanced engagement with facial expression during task conditions of contextual interference. In conclusion, whereas early components seem to be sensitive to the emotional valence of facial expression in specific contexts, late components seem to subserve interference resolution during emotional face processing.
International Journal of Psychophysiology, in press
Contextual features during recognition of facial affect are assumed to modulate the temporal course of emotional face processing. Here, we simultaneously presented colored backgrounds during valence categorizations of facial expressions. Subjects incidentally learned to perceive negative, neutral and positive expressions within a specific colored context. Subsequently, subjects made fast valence judgments while presented with the same face-color-combinations as in the first run (congruent trials) or with different face-color-combinations (incongruent trials). Incongruent trials induced significantly increased response latencies and significantly decreased performance accuracy. Contextual incongruent information during processing of neutral expressions modulated the P1 and the early posterior negativity (EPN) both localized in occipito-temporal areas. Contextual congruent information during emotional face perception revealed an emotion-related modulation of the P1 for positive expressions and of the N170 and the EPN for negative expressions. Highest amplitude of the N170 was found for negative expressions in a negatively associated context and the N170 amplitude varied with the amount of overall negative information. Incongruent trials with negative expressions elicited a parietal negativity which was localized to superior parietal cortex and which most likely represents a posterior manifestation of the N450 as an indicator of conflict processing. A sustained activation of the late LPP over parietal cortex for all incongruent trials might reflect enhanced engagement with facial expression during task conditions of contextual interference. In conclusion, whereas early components seem to be sensitive to the emotional valence of facial expression in specific contexts, late components seem to subserve interference resolution during emotional face processing.
Saturday, May 23, 2009
ARTICLE UPDATE - The Interrelations between Verbal Working Memory and Visual Selection of Emotional Faces.
Grecucci A, Soto D, Rumiati RI, Humphreys GW, Rotshtein P.
The Journal of Cognitive Neuroscience, in press
Working memory (WM) and visual selection processes interact in a reciprocal fashion based on overlapping representations abstracted from the physical characteristics of stimuli. Here, we assessed the neural basis of this interaction using facial expressions that conveyed emotion information. Participants memorized an emotional word for a later recognition test and then searched for a face of a particular gender presented in a display with two faces that differed in gender and expression. The relation between the emotional word and the expressions of the target and distractor faces was varied. RTs for the memory test were faster when the target face matched the emotional word held in WM (on valid trials) relative to when the emotional word matched the expression of the distractor (on invalid trials). There was also enhanced activation on valid compared with invalid trials in the lateral orbital gyrus, superior frontal polar (BA 10), lateral occipital sulcus, and pulvinar. Re-presentation of the WM stimulus in the search display led to the earlier onset of activity in the superior and inferior frontal gyri and the anterior hippocampus irrespective of the search validity of the re-presented stimulus. The data indicate that the middle temporal and prefrontal cortices are sensitive to the reappearance of stimuli that are held in WM, whereas a fronto-thalamic occipital network is sensitive to the behavioral significance of the match between WM and targets for selection. We conclude that these networks are modulated by high-level matches between the contents of WM, the behavioral goals, and our current sensory input.
The Journal of Cognitive Neuroscience, in press
Working memory (WM) and visual selection processes interact in a reciprocal fashion based on overlapping representations abstracted from the physical characteristics of stimuli. Here, we assessed the neural basis of this interaction using facial expressions that conveyed emotion information. Participants memorized an emotional word for a later recognition test and then searched for a face of a particular gender presented in a display with two faces that differed in gender and expression. The relation between the emotional word and the expressions of the target and distractor faces was varied. RTs for the memory test were faster when the target face matched the emotional word held in WM (on valid trials) relative to when the emotional word matched the expression of the distractor (on invalid trials). There was also enhanced activation on valid compared with invalid trials in the lateral orbital gyrus, superior frontal polar (BA 10), lateral occipital sulcus, and pulvinar. Re-presentation of the WM stimulus in the search display led to the earlier onset of activity in the superior and inferior frontal gyri and the anterior hippocampus irrespective of the search validity of the re-presented stimulus. The data indicate that the middle temporal and prefrontal cortices are sensitive to the reappearance of stimuli that are held in WM, whereas a fronto-thalamic occipital network is sensitive to the behavioral significance of the match between WM and targets for selection. We conclude that these networks are modulated by high-level matches between the contents of WM, the behavioral goals, and our current sensory input.
ARTICLE UPDATE - Decoding of Emotional Information in Voice-Sensitive Cortices.
Ethofer T, Van De Ville D, Scherer K, Vuilleumier P.
Current Biology, in press
The ability to correctly interpret emotional signals from others is crucial for successful social interaction. Previous neuroimaging studies showed that voice-sensitive auditory areas [1-3] activate to a broad spectrum of vocally expressed emotions more than to neutral speech melody (prosody). However, this enhanced response occurs irrespective of the specific emotion category, making it impossible to distinguish different vocal emotions with conventional analyses [4-8]. Here, we presented pseudowords spoken in five prosodic categories (anger, sadness, neutral, relief, joy) during event-related functional magnetic resonance imaging (fMRI), then employed multivariate pattern analysis [9, 10] to discriminate between these categories on the basis of the spatial response pattern within the auditory cortex. Our results demonstrate successful decoding of vocal emotions from fMRI responses in bilateral voice-sensitive areas, which could not be obtained by using averaged response amplitudes only. Pairwise comparisons showed that each category could be classified against all other alternatives, indicating for each emotion a specific spatial signature that generalized across speakers. These results demonstrate for the first time that emotional information is represented by distinct spatial patterns that can be decoded from brain activity in modality-specific cortical areas.
Current Biology, in press
The ability to correctly interpret emotional signals from others is crucial for successful social interaction. Previous neuroimaging studies showed that voice-sensitive auditory areas [1-3] activate to a broad spectrum of vocally expressed emotions more than to neutral speech melody (prosody). However, this enhanced response occurs irrespective of the specific emotion category, making it impossible to distinguish different vocal emotions with conventional analyses [4-8]. Here, we presented pseudowords spoken in five prosodic categories (anger, sadness, neutral, relief, joy) during event-related functional magnetic resonance imaging (fMRI), then employed multivariate pattern analysis [9, 10] to discriminate between these categories on the basis of the spatial response pattern within the auditory cortex. Our results demonstrate successful decoding of vocal emotions from fMRI responses in bilateral voice-sensitive areas, which could not be obtained by using averaged response amplitudes only. Pairwise comparisons showed that each category could be classified against all other alternatives, indicating for each emotion a specific spatial signature that generalized across speakers. These results demonstrate for the first time that emotional information is represented by distinct spatial patterns that can be decoded from brain activity in modality-specific cortical areas.
ARTICLE UPDATE - Transmission of facial expressions of emotion co-evolved with their efficient decoding in the brain: behavioral and brain evidence.
Schyns PG, Petro LS, Smith ML.
PlosOne
Competent social organisms will read the social signals of their peers. In primates, the face has evolved to transmit the organism's internal emotional state. Adaptive action suggests that the brain of the receiver has co-evolved to efficiently decode expression signals. Here, we review and integrate the evidence for this hypothesis. With a computational approach, we co-examined facial expressions as signals for data transmission and the brain as receiver and decoder of these signals. First, we show in a model observer that facial expressions form a lowly correlated signal set. Second, using time-resolved EEG data, we show how the brain uses spatial frequency information impinging on the retina to decorrelate expression categories. Between 140 to 200 ms following stimulus onset, independently in the left and right hemispheres, an information processing mechanism starts locally with encoding the eye, irrespective of expression, followed by a zooming out to processing the entire face, followed by a zooming back in to diagnostic features (e.g. the opened eyes in "fear", the mouth in "happy"). A model categorizer demonstrates that at 200 ms, the left and right brain have represented enough information to predict behavioral categorization performance.
PlosOne
Competent social organisms will read the social signals of their peers. In primates, the face has evolved to transmit the organism's internal emotional state. Adaptive action suggests that the brain of the receiver has co-evolved to efficiently decode expression signals. Here, we review and integrate the evidence for this hypothesis. With a computational approach, we co-examined facial expressions as signals for data transmission and the brain as receiver and decoder of these signals. First, we show in a model observer that facial expressions form a lowly correlated signal set. Second, using time-resolved EEG data, we show how the brain uses spatial frequency information impinging on the retina to decorrelate expression categories. Between 140 to 200 ms following stimulus onset, independently in the left and right hemispheres, an information processing mechanism starts locally with encoding the eye, irrespective of expression, followed by a zooming out to processing the entire face, followed by a zooming back in to diagnostic features (e.g. the opened eyes in "fear", the mouth in "happy"). A model categorizer demonstrates that at 200 ms, the left and right brain have represented enough information to predict behavioral categorization performance.
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