Bankó EM, Gál V, Vidnyánszky Z.
Journal of Vision, 9, 12.1-12.13
Facial emotions are important cues of human social interactions. Emotional expressions are continuously changing and thus should be monitored, memorized, and compared from time to time during social intercourse. However, it is not known how efficiently emotional expressions can be stored in short-term memory. Here we show that emotion discrimination is not impaired when the faces to be compared are separated by several seconds, requiring storage of fine-grained emotion-related information in short-term memory. Likewise, we found no significant effect of increasing the delay between the sample and the test face in the case of facial identity discrimination. Furthermore, a second experiment conducted on a large subject sample (N = 160) revealed flawless short-term memory for both facial emotions and facial identity also when observers performed the discrimination tasks only twice with novel faces. We also performed an fMRI experiment, which confirmed that discrimination of fine-grained emotional expressions in our experimental paradigm involved processing of high-level facial emotional attributes. Significantly stronger fMRI responses were found in a cortical network--including the posterior superior temporal sulcus--that is known to be involved in processing of facial emotional expression during emotion discrimination than during identity discrimination. These findings reveal flawless, high-resolution visual short-term memory for emotional expressions, which might underlie efficient monitoring of continuously changing facial emotions.
Monday, March 16, 2009
ARTICLE UPDATE - The role of mirror neurons in processing vocal emotions: evidence from psychophysiological data.
Ramachandra V, Depalma N, Lisiewski S.
International Journal of Neuroscience, 119,681-690
Recent evidence suggests that the mirror neuron system may serve as a common neural substrate for processing motor, linguistic, emotional, and other higher-level cognitive information. The current study employed psychophysiological methods to elucidate the role of this system in processing vocal emotions. Skin conductance and heart rate were measured for 25 undergraduate students while they were both listening to emotional vocalizations and also thinking (internal production) about them. The results revealed changes in skin conductance response and heart rate during both "listening" and "thinking" conditions. This suggests an active role of the mirror neuron system in processing vocal emotions.
International Journal of Neuroscience, 119,681-690
Recent evidence suggests that the mirror neuron system may serve as a common neural substrate for processing motor, linguistic, emotional, and other higher-level cognitive information. The current study employed psychophysiological methods to elucidate the role of this system in processing vocal emotions. Skin conductance and heart rate were measured for 25 undergraduate students while they were both listening to emotional vocalizations and also thinking (internal production) about them. The results revealed changes in skin conductance response and heart rate during both "listening" and "thinking" conditions. This suggests an active role of the mirror neuron system in processing vocal emotions.
Monday, March 09, 2009
ARTICLE UPDATE - Specific and common brain regions involved in the perception of faces and bodies and the representation of their emotional expression
van de Riet WA, Grezes J, de Gelder B.
Social Neuroscience, 4, 101 - 120
Many studies provide support for the role of the fusiform gyrus in face recognition and its sensitivity to emotional expressions. Recently, category-specific representation was also observed for neutral human bodies in the middle temporal/middle occipital gyrus (extrastriate body area) but it is not clear whether this area is also sensitive to emotional bodily expressions. Besides these areas, other regions that process the affective information carried by the face and the body may be common and/or specific to the face or the body. To clarify these issues we performed a systematic comparison of how the whole brain processes faces and bodies and how their affective information is represented. Participants categorized emotional facial and bodily expressions while brain activity was measured using functional magnetic resonance imaging. Our results show that, first, the amygdala and the fusiform gyrus are sensitive to recognition of facial and bodily fear signals. Secondly, the extrastriate body area-area V5/MT is specifically involved in processing bodies without being sensitive to the emotion displayed. Thirdly, other important areas such as the superior temporal sulcus, the parietal lobe and subcortical structures represent selectively facial and bodily expressions. Finally, some face/body differences in activation are a function of the emotion expressed.
Social Neuroscience, 4, 101 - 120
Many studies provide support for the role of the fusiform gyrus in face recognition and its sensitivity to emotional expressions. Recently, category-specific representation was also observed for neutral human bodies in the middle temporal/middle occipital gyrus (extrastriate body area) but it is not clear whether this area is also sensitive to emotional bodily expressions. Besides these areas, other regions that process the affective information carried by the face and the body may be common and/or specific to the face or the body. To clarify these issues we performed a systematic comparison of how the whole brain processes faces and bodies and how their affective information is represented. Participants categorized emotional facial and bodily expressions while brain activity was measured using functional magnetic resonance imaging. Our results show that, first, the amygdala and the fusiform gyrus are sensitive to recognition of facial and bodily fear signals. Secondly, the extrastriate body area-area V5/MT is specifically involved in processing bodies without being sensitive to the emotion displayed. Thirdly, other important areas such as the superior temporal sulcus, the parietal lobe and subcortical structures represent selectively facial and bodily expressions. Finally, some face/body differences in activation are a function of the emotion expressed.
Saturday, February 28, 2009
ARTICLE UPDATE - Effects of anxiety and attention control on processing pictorial and linguistic emotional information.
Reinholdt-Dunne ML, Mogg K, Bradley BP.
Behavioral Research & Therapy, in press
This study investigated the role of executive attention control in modulating selective processing of emotional information in anxiety. It was hypothesized that the combination of high anxiety and poor attention control would be associated with greater difficulty in ignoring task-irrelevant threat-related information. The study included both faces and words as stimuli. Cognitive interference effects were assessed using two emotional Stroop tasks: one with angry, fearful, happy and neutral faces, and one with threat-related, positive, and neutral words. An objective measure of attention control was obtained from the Attention network task. There were four participant groups with high/low trait anxiety and high/low attention control. Results indicated that the combination of high anxiety and poor attention control was associated with greater cognitive interference by emotional faces (including angry faces), compared to neutral faces. This interference effect was not evident in participants with high anxiety and high attentional control, or in low-anxious individuals. There was no evidence of associations between anxiety, attention control, and the interference effect of emotional words. Results indicate that high anxiety and poor attention control together predict enhanced processing of emotionally salient information, such as angry facial expressions. Implications for models of emotion processing are discussed.
Behavioral Research & Therapy, in press
This study investigated the role of executive attention control in modulating selective processing of emotional information in anxiety. It was hypothesized that the combination of high anxiety and poor attention control would be associated with greater difficulty in ignoring task-irrelevant threat-related information. The study included both faces and words as stimuli. Cognitive interference effects were assessed using two emotional Stroop tasks: one with angry, fearful, happy and neutral faces, and one with threat-related, positive, and neutral words. An objective measure of attention control was obtained from the Attention network task. There were four participant groups with high/low trait anxiety and high/low attention control. Results indicated that the combination of high anxiety and poor attention control was associated with greater cognitive interference by emotional faces (including angry faces), compared to neutral faces. This interference effect was not evident in participants with high anxiety and high attentional control, or in low-anxious individuals. There was no evidence of associations between anxiety, attention control, and the interference effect of emotional words. Results indicate that high anxiety and poor attention control together predict enhanced processing of emotionally salient information, such as angry facial expressions. Implications for models of emotion processing are discussed.
ARTICLE UPDATE - Time course and task dependence of emotion effects in word processing.
Schacht A, Sommer W.
Cognitive, Affective and Behavioral Neuroscience, 8, 28-43
The emotional content of stimuli influences cognitive performance. In two experiments, we investigated the time course and mechanisms of emotional influences on visual word processing in various tasks by recording event-related brain potentials (ERPs). The stimuli were verbs of positive, negative, and neutral valence. In Experiment 1, where lexical decisions had to be performed on single verbs, both positive and negative verbs were processed more quickly than neutral verbs and elicited a distinct ERP component, starting around 370 msec. In Experiment 2, the verbs were embedded in a semantic context provided by single nouns. Likewise, structural, lexical, and semantic decisions for positive verbs were accelerated, and an ERP effect with a scalp distribution comparable to that in Experiment 1 now started about 200 msec earlier. These effects may signal an automatic allocation of attentional resources to emotionally arousing words, since they were not modulated by different task demands. In contrast, a later ERP effect of emotion was restricted to lexical and semantic decisions and, thus, appears to indicate more elaborated, task-dependent processing of emotional words.
Cognitive, Affective and Behavioral Neuroscience, 8, 28-43
The emotional content of stimuli influences cognitive performance. In two experiments, we investigated the time course and mechanisms of emotional influences on visual word processing in various tasks by recording event-related brain potentials (ERPs). The stimuli were verbs of positive, negative, and neutral valence. In Experiment 1, where lexical decisions had to be performed on single verbs, both positive and negative verbs were processed more quickly than neutral verbs and elicited a distinct ERP component, starting around 370 msec. In Experiment 2, the verbs were embedded in a semantic context provided by single nouns. Likewise, structural, lexical, and semantic decisions for positive verbs were accelerated, and an ERP effect with a scalp distribution comparable to that in Experiment 1 now started about 200 msec earlier. These effects may signal an automatic allocation of attentional resources to emotionally arousing words, since they were not modulated by different task demands. In contrast, a later ERP effect of emotion was restricted to lexical and semantic decisions and, thus, appears to indicate more elaborated, task-dependent processing of emotional words.
ARTICLE UPDATE - Noradrenergic enhancement of amygdala responses to fear.
Onur OA, Walter H, Schlaepfer TE, Rehme AK, Schmidt C, Keysers C, Maier W, Hurlemann R.
Social Cognitive & Affective Neuroscience, in press
Multiple lines of evidence implicate the basolateral amygdala (BLA) and the noradrenergic (norepinephrine, NE) system in responding to stressful stimuli such as fear signals, suggesting hyperfunction of both in the development of stress-related pathologies including anxiety disorders. However, no causative link between elevated NE neurotransmission and BLA hyperresponsiveness to fear signals has been established to date in humans. To determine whether or not increased noradrenergic tone enhances BLA responses to fear signals, we used functional magnetic resonance imaging (fMRI) and a strategy of pharmacologically potentiating NE neurotransmission in healthy volunteers. 18 subjects were scanned two times on a facial emotion paradigm and given either a single-dose placebo or 4 mg of the selective NE reuptake inhibitor reboxetine 2 h prior to an fMRI session. We found that reboxetine induced an amygdala response bias towards fear signals that did not exist at placebo baseline. This pharmacological effect was probabilistically mapped to the BLA. Extrapolation of our data to conditions of traumatic stress suggests that disinhibited endogenous NE signaling could serve as a crucial etiological contributor to post-traumatic stress disorder (PTSD) by eliciting exaggerated BLA responses to fear signals.
Social Cognitive & Affective Neuroscience, in press
Multiple lines of evidence implicate the basolateral amygdala (BLA) and the noradrenergic (norepinephrine, NE) system in responding to stressful stimuli such as fear signals, suggesting hyperfunction of both in the development of stress-related pathologies including anxiety disorders. However, no causative link between elevated NE neurotransmission and BLA hyperresponsiveness to fear signals has been established to date in humans. To determine whether or not increased noradrenergic tone enhances BLA responses to fear signals, we used functional magnetic resonance imaging (fMRI) and a strategy of pharmacologically potentiating NE neurotransmission in healthy volunteers. 18 subjects were scanned two times on a facial emotion paradigm and given either a single-dose placebo or 4 mg of the selective NE reuptake inhibitor reboxetine 2 h prior to an fMRI session. We found that reboxetine induced an amygdala response bias towards fear signals that did not exist at placebo baseline. This pharmacological effect was probabilistically mapped to the BLA. Extrapolation of our data to conditions of traumatic stress suggests that disinhibited endogenous NE signaling could serve as a crucial etiological contributor to post-traumatic stress disorder (PTSD) by eliciting exaggerated BLA responses to fear signals.
Saturday, February 21, 2009
ARTICLE UPDATE - The set switching function of nonclinical dissociators under negative emotion.
Chiu CD, Yeh YY, Huang YM, Wu YC, Chiu YC.
Journal of Abnormal Psychology, 118, 214-222
Rapid switching may underlie the disruption of some integrated thought processes that characterize dissociation in both nonclinical and clinical populations. We investigated the set switching function under negative emotion with three groups of nonclinical participants that had different degrees of dissociation proneness. In the experiment, participants judged whether the digit in a predefined target color was odd or even on the preswitch trials. In a perseverance condition, participants were required to switch to a new target color while the previous target color became the distractor color. In a learned irrelevance condition, the previously ignored color became the new target color. The results showed that the three groups did not differ in focusing attention in the preswitch trials, for set switching in the baseline condition (in which emotion was not engaged), or for switching in the learned irrelevance condition under negative emotion. However, high dissociators under negative emotion showed faster switching in the perseverance condition. This enhanced ability to divert attention to a new mental set under negative emotion may be a coping strategy related to cognitive symptoms in dissociative disorders.
Journal of Abnormal Psychology, 118, 214-222
Rapid switching may underlie the disruption of some integrated thought processes that characterize dissociation in both nonclinical and clinical populations. We investigated the set switching function under negative emotion with three groups of nonclinical participants that had different degrees of dissociation proneness. In the experiment, participants judged whether the digit in a predefined target color was odd or even on the preswitch trials. In a perseverance condition, participants were required to switch to a new target color while the previous target color became the distractor color. In a learned irrelevance condition, the previously ignored color became the new target color. The results showed that the three groups did not differ in focusing attention in the preswitch trials, for set switching in the baseline condition (in which emotion was not engaged), or for switching in the learned irrelevance condition under negative emotion. However, high dissociators under negative emotion showed faster switching in the perseverance condition. This enhanced ability to divert attention to a new mental set under negative emotion may be a coping strategy related to cognitive symptoms in dissociative disorders.
Friday, February 13, 2009
ARTICLE UPDATE - Influence of intermixed emotion-relevant trials on the affective Simon effect.
Zhang Y, Proctor RW.
Experimental Psychology, 55, 409-416
"Good" and "bad" vocal responses are faster when an irrelevant emotional stimulus feature corresponds with the response than when it does not, a phenomenon known as the affective Simon effect. Two experiments investigated how this effect was influenced by an intermixed emotion-relevant evaluation task. In Experiment 1, four schematic faces (friendly, happy, hostile, sad) were used for the affective Simon task and four different images (bird, heart, gun, ghost) for the evaluation task, whereas in Experiment 2 the schematic faces were used for both tasks. Mixed-compatible emotion-relevant trials increased the affective Simon effect in both experiments, but mixed-incompatible emotion-relevant trials did not influence it. Also, the advantage of the compatible mapping over the incompatible mapping increased in mixed conditions rather than decreased. These results differ from those obtained when visual-manual tasks for which location is relevant and irrelevant are mixed. They confirm that enhancement of the affective Simon effect when the Simon task is mixed with a compatible emotion-relevant task is due to increased salience of the affective valence.
Experimental Psychology, 55, 409-416
"Good" and "bad" vocal responses are faster when an irrelevant emotional stimulus feature corresponds with the response than when it does not, a phenomenon known as the affective Simon effect. Two experiments investigated how this effect was influenced by an intermixed emotion-relevant evaluation task. In Experiment 1, four schematic faces (friendly, happy, hostile, sad) were used for the affective Simon task and four different images (bird, heart, gun, ghost) for the evaluation task, whereas in Experiment 2 the schematic faces were used for both tasks. Mixed-compatible emotion-relevant trials increased the affective Simon effect in both experiments, but mixed-incompatible emotion-relevant trials did not influence it. Also, the advantage of the compatible mapping over the incompatible mapping increased in mixed conditions rather than decreased. These results differ from those obtained when visual-manual tasks for which location is relevant and irrelevant are mixed. They confirm that enhancement of the affective Simon effect when the Simon task is mixed with a compatible emotion-relevant task is due to increased salience of the affective valence.
ARTICLE UPDATE - Motivated and controlled attention to emotion: Time-course of the late positive potential.
Hajcak G, Dunning JP, Foti D.
Clinical Neurophysiology, in press
OBJECTIVE: The present study examined the time-course of automatic and controlled modulation of the late positive potential (LPP) during emotional picture viewing. METHODS: Participants (N=32) viewed neutral and unpleasant stimuli for 6000ms; at 3000ms, one of two tones signaled participants to attend either to a more or less arousing portion of the picture. The time-course of the LPP was examined both during the passive viewing and directed attention portions of the trial using the method proposed by Guthrie and Buchwald [Guthrie D, Buchwald JS. Significance testing of difference potentials. Psychophysiology 1991;28(2):240-4]. RESULTS: During passive viewing, the LPP became reliably larger following the presentation of unpleasant pictures from 160ms onward; the magnitude of the LPP became reliably smaller beginning 620ms after participants were instructed to attend to the less arousing aspects of unpleasant pictures - and this difference was maintained throughout the duration of the trial. CONCLUSIONS: The LPP reflects relatively automatic attention to emotional visual stimuli, but is also sensitive to manipulations of directed attention toward arousing versus neutral aspects of such stimuli. SIGNIFICANCE: These results shed further light on the time-course of emotional and cognitive modulation of the LPP, and suggest that the LPP reflects the relatively rapid and dynamic allocation of increased attention to emotional stimuli.
Clinical Neurophysiology, in press
OBJECTIVE: The present study examined the time-course of automatic and controlled modulation of the late positive potential (LPP) during emotional picture viewing. METHODS: Participants (N=32) viewed neutral and unpleasant stimuli for 6000ms; at 3000ms, one of two tones signaled participants to attend either to a more or less arousing portion of the picture. The time-course of the LPP was examined both during the passive viewing and directed attention portions of the trial using the method proposed by Guthrie and Buchwald [Guthrie D, Buchwald JS. Significance testing of difference potentials. Psychophysiology 1991;28(2):240-4]. RESULTS: During passive viewing, the LPP became reliably larger following the presentation of unpleasant pictures from 160ms onward; the magnitude of the LPP became reliably smaller beginning 620ms after participants were instructed to attend to the less arousing aspects of unpleasant pictures - and this difference was maintained throughout the duration of the trial. CONCLUSIONS: The LPP reflects relatively automatic attention to emotional visual stimuli, but is also sensitive to manipulations of directed attention toward arousing versus neutral aspects of such stimuli. SIGNIFICANCE: These results shed further light on the time-course of emotional and cognitive modulation of the LPP, and suggest that the LPP reflects the relatively rapid and dynamic allocation of increased attention to emotional stimuli.
ARTICLE UPDATE - Mood influences supraspinal pain processing separately from attention.
Villemure C, Bushnell MC.
Journal of Neuroscience, 29, 705 - 715
Studies show that inducing a positive mood or diverting attention from pain decreases pain perception. Nevertheless, induction manipulations, such as viewing interesting movies or performing mathematical tasks, often influence both emotional and attentional states. Imaging studies have examined the neural basis of psychological pain modulation, but none has explicitly separated the effects of emotion and attention. Using odors to modulate mood and shift attention from pain, we previously showed that the perceptual consequences of changing mood differed from those of altering attention, with mood primarily altering pain unpleasantness and attention preferentially altering pain intensity. These findings suggest that brain circuits involved in pain modulation provoked by mood or attention are partially separable. Here we used functional magnetic resonance imaging to directly compare the neurocircuitry involved in mood- and attention-related pain modulation. We manipulated independently mood state and attention direction, using tasks involving heat pain and pleasant and unpleasant odors. Pleasant odors, independent of attentional focus, induced positive mood changes and decreased pain unpleasantness and pain-related activity within the anterior cingulate (ACC), medial thalamus, and primary and secondary somatosensory cortices. The effects of attentional state were less robust, with only the activity in anterior insular cortex (aIC) showing possible attentional modulation. Lateral inferior frontal cortex [LinfF; Brodmann's area (BA) 45/47] activity correlated with mood-related modulation, whereas superior posterior parietal (SPP; BA7) and entorhinal activity correlated with attention-related modulation. ACC activity covaried with LinfF and periacqueductal gray activity, whereas aIC activity covaried with SPP activity. These findings suggest that separate neuromodulatory circuits underlie emotional and attentional modulation of pain.
Journal of Neuroscience, 29, 705 - 715
Studies show that inducing a positive mood or diverting attention from pain decreases pain perception. Nevertheless, induction manipulations, such as viewing interesting movies or performing mathematical tasks, often influence both emotional and attentional states. Imaging studies have examined the neural basis of psychological pain modulation, but none has explicitly separated the effects of emotion and attention. Using odors to modulate mood and shift attention from pain, we previously showed that the perceptual consequences of changing mood differed from those of altering attention, with mood primarily altering pain unpleasantness and attention preferentially altering pain intensity. These findings suggest that brain circuits involved in pain modulation provoked by mood or attention are partially separable. Here we used functional magnetic resonance imaging to directly compare the neurocircuitry involved in mood- and attention-related pain modulation. We manipulated independently mood state and attention direction, using tasks involving heat pain and pleasant and unpleasant odors. Pleasant odors, independent of attentional focus, induced positive mood changes and decreased pain unpleasantness and pain-related activity within the anterior cingulate (ACC), medial thalamus, and primary and secondary somatosensory cortices. The effects of attentional state were less robust, with only the activity in anterior insular cortex (aIC) showing possible attentional modulation. Lateral inferior frontal cortex [LinfF; Brodmann's area (BA) 45/47] activity correlated with mood-related modulation, whereas superior posterior parietal (SPP; BA7) and entorhinal activity correlated with attention-related modulation. ACC activity covaried with LinfF and periacqueductal gray activity, whereas aIC activity covaried with SPP activity. These findings suggest that separate neuromodulatory circuits underlie emotional and attentional modulation of pain.
ARTICLE UPDATE - Attentional control of emotional distraction in rapid serial visual presentation.
Peers PV, Lawrence AD.
Emotion, 9, 140 - 145
Temperament research has highlighted the importance of attentional control in both emotion regulation and as a predictor of psychopathology. Enhanced susceptibility to emotional distraction is a key feature of mood disturbance. Whereas many studies have examined the influence of individual differences in anxiety on the disruptive effects of emotional distractors, individual differences in attentional control have been largely neglected. Here we examine, within healthy volunteers, the relative contributions of individual differences in self-reported anxiety and attentional control to distractibility caused by emotional or neutral faces distractors occurring prior to neutral face targets during rapid serial visual presentation. Participants with good attentional control were less affected by both neutral and emotional distractors than participants with poorer attentional control. More pronounced distraction deficits were seen for emotional relative to neutral distractors in individuals with poor attentional control. In contrast state anxiety was not associated with increased emotional distraction. Our findings suggest a protective role of attentional control mechanisms in minimizing the influence of emotional distraction.
Emotion, 9, 140 - 145
Temperament research has highlighted the importance of attentional control in both emotion regulation and as a predictor of psychopathology. Enhanced susceptibility to emotional distraction is a key feature of mood disturbance. Whereas many studies have examined the influence of individual differences in anxiety on the disruptive effects of emotional distractors, individual differences in attentional control have been largely neglected. Here we examine, within healthy volunteers, the relative contributions of individual differences in self-reported anxiety and attentional control to distractibility caused by emotional or neutral faces distractors occurring prior to neutral face targets during rapid serial visual presentation. Participants with good attentional control were less affected by both neutral and emotional distractors than participants with poorer attentional control. More pronounced distraction deficits were seen for emotional relative to neutral distractors in individuals with poor attentional control. In contrast state anxiety was not associated with increased emotional distraction. Our findings suggest a protective role of attentional control mechanisms in minimizing the influence of emotional distraction.
ARTICLE UPDATE - The effects of emotional intensity on ERP correlates of recognition memory
Schaefer A, Fletcher K, Pottage CL, Alexander K, Brown C.
Neuroreport, 20, 319 - 324
The effects of negative emotional intensity on memory-related brain activity were tested by using human scalp event-related potentials (ERP). A neural index of memory function - the electrophysiological 'Old-New' effect - was obtained from participants undertaking a memory recognition test of previously studied ('old') and unstudied ('new') pictures of variable levels of negative emotional intensity. The magnitude of the old-new effect was compared across four different levels of linearly increasing stimulus emotional intensity. Results revealed an inverted-U-shaped effect of emotional intensity on the magnitude of ERP old-new differences starting at 300 ms after stimulus onset. These results suggest that moderate negative emotions can enhance memory brain function, whereas extreme levels of emotional intensity have the potential of inhibiting memory function. Results are discussed in terms of their implications for neurobiological and psychological models of emotion-memory interactions.
Neuroreport, 20, 319 - 324
The effects of negative emotional intensity on memory-related brain activity were tested by using human scalp event-related potentials (ERP). A neural index of memory function - the electrophysiological 'Old-New' effect - was obtained from participants undertaking a memory recognition test of previously studied ('old') and unstudied ('new') pictures of variable levels of negative emotional intensity. The magnitude of the old-new effect was compared across four different levels of linearly increasing stimulus emotional intensity. Results revealed an inverted-U-shaped effect of emotional intensity on the magnitude of ERP old-new differences starting at 300 ms after stimulus onset. These results suggest that moderate negative emotions can enhance memory brain function, whereas extreme levels of emotional intensity have the potential of inhibiting memory function. Results are discussed in terms of their implications for neurobiological and psychological models of emotion-memory interactions.
ARTICLE UPDATE- Orienting to threat: faster localization of fearful facial expressions and body postures revealed by saccadic eye movements.
Bannerman RL, Milders M, de Gelder B, Sahraie A.
Proceedings in Biological Science, in press
Most studies investigating speeded orientation towards threat have used manual responses. By measuring orienting behaviour using eye movements a more direct and ecologically valid measure of attention can be made. Here, we used a forced-choice saccadic and manual localization task to investigate the speed of discrimination for fearful and neutral body and face images. Fearful/neutral body or face pairs were bilaterally presented for either 20 or 500ms. Results showed faster saccadic orienting to fearful body and face emotions compared with neutral only at the shortest presentation time (20ms). For manual responses, faster discrimination of fearful bodies and faces was observed only at the longest duration (500ms). More errors were made when localizing neutral targets, suggesting that fearful bodies and faces may have captured attention automatically. Results were not attributable to low-level image properties as no threat bias, in terms of reaction time or accuracy, was observed for inverted presentation. Taken together, the results suggest faster localization of threat conveyed both by the face and the body within the oculomotor system. In addition, enhanced detection of fearful body postures suggests that we can readily recognize threat-related information conveyed by body postures in the absence of any face cues.
Proceedings in Biological Science, in press
Most studies investigating speeded orientation towards threat have used manual responses. By measuring orienting behaviour using eye movements a more direct and ecologically valid measure of attention can be made. Here, we used a forced-choice saccadic and manual localization task to investigate the speed of discrimination for fearful and neutral body and face images. Fearful/neutral body or face pairs were bilaterally presented for either 20 or 500ms. Results showed faster saccadic orienting to fearful body and face emotions compared with neutral only at the shortest presentation time (20ms). For manual responses, faster discrimination of fearful bodies and faces was observed only at the longest duration (500ms). More errors were made when localizing neutral targets, suggesting that fearful bodies and faces may have captured attention automatically. Results were not attributable to low-level image properties as no threat bias, in terms of reaction time or accuracy, was observed for inverted presentation. Taken together, the results suggest faster localization of threat conveyed both by the face and the body within the oculomotor system. In addition, enhanced detection of fearful body postures suggests that we can readily recognize threat-related information conveyed by body postures in the absence of any face cues.
Friday, January 16, 2009
ARTICLE UPDATE - Dissociable neural effects of stimulus valence and preceding context during the inhibition of responses to emotional faces.
Schulz KP, Clerkin SM, Halperin JM, Newcorn JH, Tang CY, Fan J.
Human Brain Mapping, in press
Socially appropriate behavior requires the concurrent inhibition of actions that are inappropriate in the context. This self-regulatory function requires an interaction of inhibitory and emotional processes that recruits brain regions beyond those engaged by either processes alone. In this study, we isolated brain activity associated with response inhibition and emotional processing in 24 healthy adults using event-related functional magnetic resonance imaging (fMRI) and a go/no-go task that independently manipulated the context preceding no-go trials (ie, number of go trials) and the valence (ie, happy, sad, and neutral) of the face stimuli used as trial cues. Parallel quadratic trends were seen in correct inhibitions on no-go trials preceded by increasing numbers of go trials and associated activation for correct no-go trials in inferior frontal gyrus pars opercularis, pars triangularis, and pars orbitalis, temporoparietal junction, superior parietal lobule, and temporal sensory association cortices. Conversely, the comparison of happy versus neutral faces and sad versus neutral faces revealed valence-dependent activation in the amygdala, anterior insula cortex, and posterior midcingulate cortex. Further, an interaction between inhibition and emotion was seen in valence-dependent variations in the quadratic trend in no-go activation in the right inferior frontal gyrus and left posterior insula cortex. These results suggest that the inhibition of response to emotional cues involves the interaction of partly dissociable limbic and frontoparietal networks that encode emotional cues and use these cues to exert inhibitory control over the motor, attention, and sensory functions needed to perform the task, respectively.
Human Brain Mapping, in press
Socially appropriate behavior requires the concurrent inhibition of actions that are inappropriate in the context. This self-regulatory function requires an interaction of inhibitory and emotional processes that recruits brain regions beyond those engaged by either processes alone. In this study, we isolated brain activity associated with response inhibition and emotional processing in 24 healthy adults using event-related functional magnetic resonance imaging (fMRI) and a go/no-go task that independently manipulated the context preceding no-go trials (ie, number of go trials) and the valence (ie, happy, sad, and neutral) of the face stimuli used as trial cues. Parallel quadratic trends were seen in correct inhibitions on no-go trials preceded by increasing numbers of go trials and associated activation for correct no-go trials in inferior frontal gyrus pars opercularis, pars triangularis, and pars orbitalis, temporoparietal junction, superior parietal lobule, and temporal sensory association cortices. Conversely, the comparison of happy versus neutral faces and sad versus neutral faces revealed valence-dependent activation in the amygdala, anterior insula cortex, and posterior midcingulate cortex. Further, an interaction between inhibition and emotion was seen in valence-dependent variations in the quadratic trend in no-go activation in the right inferior frontal gyrus and left posterior insula cortex. These results suggest that the inhibition of response to emotional cues involves the interaction of partly dissociable limbic and frontoparietal networks that encode emotional cues and use these cues to exert inhibitory control over the motor, attention, and sensory functions needed to perform the task, respectively.
ARTICLE UPDATE - Emotions in word and face processing: Early and late cortical responses.
Emotions in word and face processing: Early and late cortical responses.
Brain & Cognition, in press
Recent research suggests that emotion effects in word processing resemble those in other stimulus domains such as pictures or faces. The present study aims to provide more direct evidence for this notion by comparing emotion effects in word and face processing in a within-subject design. Event-related brain potentials (ERPs) were recorded as participants made decisions on the lexicality of emotionally positive, negative, and neutral German verbs or pseudowords, and on the integrity of intact happy, angry, and neutral faces or slightly distorted faces. Relative to neutral and negative stimuli both positive verbs and happy faces elicited posterior ERP negativities that were indistinguishable in scalp distribution and resembled the early posterior negativities reported by others. Importantly, these ERP modulations appeared at very different latencies. Therefore, it appears that similar brain systems reflect the decoding of both biological and symbolic emotional signals of positive valence, differing mainly in the speed of meaning access, which is more direct and faster for facial expressions than for words.
Brain & Cognition, in press
Recent research suggests that emotion effects in word processing resemble those in other stimulus domains such as pictures or faces. The present study aims to provide more direct evidence for this notion by comparing emotion effects in word and face processing in a within-subject design. Event-related brain potentials (ERPs) were recorded as participants made decisions on the lexicality of emotionally positive, negative, and neutral German verbs or pseudowords, and on the integrity of intact happy, angry, and neutral faces or slightly distorted faces. Relative to neutral and negative stimuli both positive verbs and happy faces elicited posterior ERP negativities that were indistinguishable in scalp distribution and resembled the early posterior negativities reported by others. Importantly, these ERP modulations appeared at very different latencies. Therefore, it appears that similar brain systems reflect the decoding of both biological and symbolic emotional signals of positive valence, differing mainly in the speed of meaning access, which is more direct and faster for facial expressions than for words.
ARTICLE UPDATE - Functional connectivity of the human amygdala using resting state fMRI.
Roy AK, Shehzad Z, Margulies DS, Kelly AM, Uddin LQ, Gotimer K, Biswal BB, Castellanos FX, Milham MP.
Neuroimage, in press
The amygdala is composed of structurally and functionally distinct nuclei that contribute to the processing of emotion through interactions with other subcortical and cortical structures. While these circuits have been studied extensively in animals, human neuroimaging investigations of amygdala-based networks have typically considered the amygdala as a single structure, which likely masks contributions of individual amygdala subdivisions. The present study uses resting state functional magnetic resonance imaging (fMRI) to test whether distinct functional connectivity patterns, like those observed in animal studies, can be detected across three amygdala subdivisions: laterobasal, centromedial, and superficial. In a sample of 65 healthy adults, voxelwise regression analyses demonstrated positively-predicted ventral and negatively-predicted dorsal networks associated with the total amygdala, consistent with previous animal and human studies. Investigation of individual amygdala subdivisions revealed distinct differences in connectivity patterns within the amygdala and throughout the brain. Spontaneous activity in the laterobasal subdivision predicted activity in temporal and frontal regions, while activity in the centromedial nuclei predicted activity primarily in striatum. Activity in the superficial subdivision positively predicted activity throughout the limbic lobe. These findings suggest that resting state fMRI can be used to investigate human amygdala networks at a greater level of detail than previously appreciated, allowing for the further advancement of translational models.
Neuroimage, in press
The amygdala is composed of structurally and functionally distinct nuclei that contribute to the processing of emotion through interactions with other subcortical and cortical structures. While these circuits have been studied extensively in animals, human neuroimaging investigations of amygdala-based networks have typically considered the amygdala as a single structure, which likely masks contributions of individual amygdala subdivisions. The present study uses resting state functional magnetic resonance imaging (fMRI) to test whether distinct functional connectivity patterns, like those observed in animal studies, can be detected across three amygdala subdivisions: laterobasal, centromedial, and superficial. In a sample of 65 healthy adults, voxelwise regression analyses demonstrated positively-predicted ventral and negatively-predicted dorsal networks associated with the total amygdala, consistent with previous animal and human studies. Investigation of individual amygdala subdivisions revealed distinct differences in connectivity patterns within the amygdala and throughout the brain. Spontaneous activity in the laterobasal subdivision predicted activity in temporal and frontal regions, while activity in the centromedial nuclei predicted activity primarily in striatum. Activity in the superficial subdivision positively predicted activity throughout the limbic lobe. These findings suggest that resting state fMRI can be used to investigate human amygdala networks at a greater level of detail than previously appreciated, allowing for the further advancement of translational models.
ARTICLE UPDATE - Dissociable processes underlying decisions in the Iowa Gambling Task: A new integrative framework.
Stocco A, Fum D, Napoli A.
Behavioral and Brain Functions, in press
ABSTRACT: BACKGROUND: The Iowa Gambling Task (IGT) is a common paradigm used to study the interactions between emotions and decision making, yet little consensus exists on the cognitive process determining participants' decisions, what affects them, and how these processes interact with each other. A novel conceptual framework is proposed according to which behavior in the IGT reflects a balance between two dissociable processes; a cognitively demanding process that tracks each option's long-term payoff, and a lower-level, automatic process that is primarily sensitive to loss frequency and magnitude. METHODS: A behavioral experiment was carried out with a modified version of IGT. In this modified version, participants went through an additional phase of interaction, designed to measure performance without further learning, in which no feedback on individual decisions was given. A secondary distractor task was presented in either the first or the second phase of the experiment. Behavioral measures of performance tracking both payoff and frequency sensitivity in choices were collected throughout the experiment. RESULTS: Consistent with our framework, the results confirmed that: (a) the two competing cognitive processes can be dissociated; (b) that learning from decision outcomes requires central cognitive resources to estimate long-term payoff; and (c) that the decision phase itself can be carried out during an interfering task once learning has occurred. CONCLUSIONS: The experimental results support our novel description of the cognitive processes underlying performance in the Iowa Gambling Task. They also suggest that patients' impairments in this and other gambling paradigms can originate from a number of different causes, including a failure in allocating resources among cognitive strategies. This latter interpretation might be particularly useful in explaining the impairments of patients with ventromedial prefrontal cortex lesions and, by extension, the contribution of this brain region to human decision making.
Behavioral and Brain Functions, in press
ABSTRACT: BACKGROUND: The Iowa Gambling Task (IGT) is a common paradigm used to study the interactions between emotions and decision making, yet little consensus exists on the cognitive process determining participants' decisions, what affects them, and how these processes interact with each other. A novel conceptual framework is proposed according to which behavior in the IGT reflects a balance between two dissociable processes; a cognitively demanding process that tracks each option's long-term payoff, and a lower-level, automatic process that is primarily sensitive to loss frequency and magnitude. METHODS: A behavioral experiment was carried out with a modified version of IGT. In this modified version, participants went through an additional phase of interaction, designed to measure performance without further learning, in which no feedback on individual decisions was given. A secondary distractor task was presented in either the first or the second phase of the experiment. Behavioral measures of performance tracking both payoff and frequency sensitivity in choices were collected throughout the experiment. RESULTS: Consistent with our framework, the results confirmed that: (a) the two competing cognitive processes can be dissociated; (b) that learning from decision outcomes requires central cognitive resources to estimate long-term payoff; and (c) that the decision phase itself can be carried out during an interfering task once learning has occurred. CONCLUSIONS: The experimental results support our novel description of the cognitive processes underlying performance in the Iowa Gambling Task. They also suggest that patients' impairments in this and other gambling paradigms can originate from a number of different causes, including a failure in allocating resources among cognitive strategies. This latter interpretation might be particularly useful in explaining the impairments of patients with ventromedial prefrontal cortex lesions and, by extension, the contribution of this brain region to human decision making.
ARTICLE UPDATE - The emotional blink: Adult age differences in visual attention to emotional information.
Langley LK, Rokke PD, Stark AC, Saville AL, Allen JL, Bagne AG.
Psycholoyg & Aging, 23, 873-885
To assess age differences in attention-emotion interactions, the authors asked young adults (ages 18-33 years) and older adults (ages 60-80 years) to identify target words in a rapid serial visual presentation (RSVP) task. The second of two target words was neutral or emotional in content (positive in Experiment 1, negative in Experiment 2). In general, the ability to identify targets from a word stream declined with age. Age differences specific to the attentional blink were greatly reduced when baseline detection accuracy was equated between groups. With regard to emotion effects, older adults showed enhanced identification of both positive and negative words relative to neutral words, whereas young adults showed enhanced identification of positive words and reduced identification of negative words. Together these findings suggest that the nature of attention-emotion interactions changes with age, but there was little support for a motivational shift consistent with emotional regulation goals at an early stage of cognitive processing.
Psycholoyg & Aging, 23, 873-885
To assess age differences in attention-emotion interactions, the authors asked young adults (ages 18-33 years) and older adults (ages 60-80 years) to identify target words in a rapid serial visual presentation (RSVP) task. The second of two target words was neutral or emotional in content (positive in Experiment 1, negative in Experiment 2). In general, the ability to identify targets from a word stream declined with age. Age differences specific to the attentional blink were greatly reduced when baseline detection accuracy was equated between groups. With regard to emotion effects, older adults showed enhanced identification of both positive and negative words relative to neutral words, whereas young adults showed enhanced identification of positive words and reduced identification of negative words. Together these findings suggest that the nature of attention-emotion interactions changes with age, but there was little support for a motivational shift consistent with emotional regulation goals at an early stage of cognitive processing.
ARTICLE UPDATE - Behavioral triggers of skin conductance responses and their neural correlates in the primate amygdala.
Laine CM, Spitler KM, Mosher CP, Gothard KM.
Journal of Neurophysiology, in press
The amygdala plays a crucial role in evaluating the emotional significance of stimuli and in transforming the results of this evaluation into appropriate autonomic responses. Lesion and stimulation studies suggest involvement of the amygdala in the generation of the skin conductance response (SCR), which is an indirect measure of autonomic activity that has been associated with both emotion and attention. It is unclear if this involvement marks an emotional reaction to an external stimulus, or sympathetic arousal regardless of its origin. We recorded skin conductance in parallel with single unit activity from the right amygdala of two rhesus monkeys during a rewarded image viewing task, and while the monkeys sat alone in a dimly lit room, drifting in and out of sleep. In both experimental conditions, we found similar SCR-related modulation of activity at the single unit and population level. This suggests that the amygdala contributes to the production or modulation of SCRs regardless of the source of sympathetic arousal.
Journal of Neurophysiology, in press
The amygdala plays a crucial role in evaluating the emotional significance of stimuli and in transforming the results of this evaluation into appropriate autonomic responses. Lesion and stimulation studies suggest involvement of the amygdala in the generation of the skin conductance response (SCR), which is an indirect measure of autonomic activity that has been associated with both emotion and attention. It is unclear if this involvement marks an emotional reaction to an external stimulus, or sympathetic arousal regardless of its origin. We recorded skin conductance in parallel with single unit activity from the right amygdala of two rhesus monkeys during a rewarded image viewing task, and while the monkeys sat alone in a dimly lit room, drifting in and out of sleep. In both experimental conditions, we found similar SCR-related modulation of activity at the single unit and population level. This suggests that the amygdala contributes to the production or modulation of SCRs regardless of the source of sympathetic arousal.
Sunday, December 21, 2008
ARTICLE UPDATE - Decoding face information in time, frequency and space from direct intracranial recordings of the human brain.
Tsuchiya N, Kawasaki H, Oya H, Howard MA 3rd, Adolphs R.
PLoS One, in press
Faces are processed by a neural system with distributed anatomical components, but the roles of these components remain unclear. A dominant theory of face perception postulates independent representations of invariant aspects of faces (e.g., identity) in ventral temporal cortex including the fusiform gyrus, and changeable aspects of faces (e.g., emotion) in lateral temporal cortex including the superior temporal sulcus. Here we recorded neuronal activity directly from the cortical surface in 9 neurosurgical subjects undergoing epilepsy monitoring while they viewed static and dynamic facial expressions. Applying novel decoding analyses to the power spectrogram of electrocorticograms (ECoG) from over 100 contacts in ventral and lateral temporal cortex, we found better representation of both invariant and changeable aspects of faces in ventral than lateral temporal cortex. Critical information for discriminating faces from geometric patterns was carried by power modulations between 50 to 150 Hz. For both static and dynamic face stimuli, we obtained a higher decoding performance in ventral than lateral temporal cortex. For discriminating fearful from happy expressions, critical information was carried by power modulation between 60-150 Hz and below 30 Hz, and again better decoded in ventral than lateral temporal cortex. Task-relevant attention improved decoding accuracy more than 10% across a wide frequency range in ventral but not at all in lateral temporal cortex. Spatial searchlight decoding showed that decoding performance was highest around the middle fusiform gyrus. Finally, we found that the right hemisphere, in general, showed superior decoding to the left hemisphere. Taken together, our results challenge the dominant model for independent face representation of invariant and changeable aspects: information about both face attributes was better decoded from a single region in the middle fusiform gyrus.
PLoS One, in press
Faces are processed by a neural system with distributed anatomical components, but the roles of these components remain unclear. A dominant theory of face perception postulates independent representations of invariant aspects of faces (e.g., identity) in ventral temporal cortex including the fusiform gyrus, and changeable aspects of faces (e.g., emotion) in lateral temporal cortex including the superior temporal sulcus. Here we recorded neuronal activity directly from the cortical surface in 9 neurosurgical subjects undergoing epilepsy monitoring while they viewed static and dynamic facial expressions. Applying novel decoding analyses to the power spectrogram of electrocorticograms (ECoG) from over 100 contacts in ventral and lateral temporal cortex, we found better representation of both invariant and changeable aspects of faces in ventral than lateral temporal cortex. Critical information for discriminating faces from geometric patterns was carried by power modulations between 50 to 150 Hz. For both static and dynamic face stimuli, we obtained a higher decoding performance in ventral than lateral temporal cortex. For discriminating fearful from happy expressions, critical information was carried by power modulation between 60-150 Hz and below 30 Hz, and again better decoded in ventral than lateral temporal cortex. Task-relevant attention improved decoding accuracy more than 10% across a wide frequency range in ventral but not at all in lateral temporal cortex. Spatial searchlight decoding showed that decoding performance was highest around the middle fusiform gyrus. Finally, we found that the right hemisphere, in general, showed superior decoding to the left hemisphere. Taken together, our results challenge the dominant model for independent face representation of invariant and changeable aspects: information about both face attributes was better decoded from a single region in the middle fusiform gyrus.
ARTICLE UPDATE - EEG-MEG evidence for early differential repetition effects for fearful, happy and neutral faces.
Morel S, Ponz A, Mercier M, Vuilleumier P, George N.
Brain Research, in press
To determine how emotional information modulates subsequent traces for repeated stimuli, we combined simultaneous electro-encephalography (EEG) and magneto-encephalography (MEG) measures during long-lag incidental repetition of fearful, happy, and neutral faces. Repetition effects were modulated by facial expression in three different time windows, starting as early as 40-50 ms in both EEG and MEG, then arising at the time of the N170/M170, and finally between 280-320 ms in MEG only. The very early repetition effect, observed at 40-50 ms over occipito-temporo-parietal regions, showed a different MEG topography according to the facial expression. This differential response to fearful, happy and neutral faces suggests the existence of very early discriminative visual processing of expressive faces, possibly based on the low-level physical features typical of different emotions. The N170 and M170 face-selective components both showed repetition enhancement selective to neutral faces, with greater amplitude for emotional than neutral faces on the first but not the second presentation. These differential repetition effects may reflect valence acquisition for the neutral faces due to repetition, and suggest a combined influence of emotion- and experience-related factors on the early stage of face encoding. Finally, later repetition effects consisted in enhanced M300 (MEG) between 280 and 320 ms for fearful relative to happy and neutral faces that occurred on the first presentation, but levelled out on the second presentation. This effect may correspond to the higher arousing value of fearful stimuli that might habituate with repetition. Our results reveal that multiple stages of face processing are affected by the repetition of emotional information.
Brain Research, in press
To determine how emotional information modulates subsequent traces for repeated stimuli, we combined simultaneous electro-encephalography (EEG) and magneto-encephalography (MEG) measures during long-lag incidental repetition of fearful, happy, and neutral faces. Repetition effects were modulated by facial expression in three different time windows, starting as early as 40-50 ms in both EEG and MEG, then arising at the time of the N170/M170, and finally between 280-320 ms in MEG only. The very early repetition effect, observed at 40-50 ms over occipito-temporo-parietal regions, showed a different MEG topography according to the facial expression. This differential response to fearful, happy and neutral faces suggests the existence of very early discriminative visual processing of expressive faces, possibly based on the low-level physical features typical of different emotions. The N170 and M170 face-selective components both showed repetition enhancement selective to neutral faces, with greater amplitude for emotional than neutral faces on the first but not the second presentation. These differential repetition effects may reflect valence acquisition for the neutral faces due to repetition, and suggest a combined influence of emotion- and experience-related factors on the early stage of face encoding. Finally, later repetition effects consisted in enhanced M300 (MEG) between 280 and 320 ms for fearful relative to happy and neutral faces that occurred on the first presentation, but levelled out on the second presentation. This effect may correspond to the higher arousing value of fearful stimuli that might habituate with repetition. Our results reveal that multiple stages of face processing are affected by the repetition of emotional information.
ARTICLE UPDATE - Dissociable neural effects of stimulus valence and preceding context during the inhibition of responses to emotional faces.
Schulz KP, Clerkin SM, Halperin JM, Newcorn JH, Tang CY, Fan J.
Human Brain Mapping, in press
Socially appropriate behavior requires the concurrent inhibition of actions that are inappropriate in the context. This self-regulatory function requires an interaction of inhibitory and emotional processes that recruits brain regions beyond those engaged by either processes alone. In this study, we isolated brain activity associated with response inhibition and emotional processing in 24 healthy adults using event-related functional magnetic resonance imaging (fMRI) and a go/no-go task that independently manipulated the context preceding no-go trials (ie, number of go trials) and the valence (ie, happy, sad, and neutral) of the face stimuli used as trial cues. Parallel quadratic trends were seen in correct inhibitions on no-go trials preceded by increasing numbers of go trials and associated activation for correct no-go trials in inferior frontal gyrus pars opercularis, pars triangularis, and pars orbitalis, temporoparietal junction, superior parietal lobule, and temporal sensory association cortices. Conversely, the comparison of happy versus neutral faces and sad versus neutral faces revealed valence-dependent activation in the amygdala, anterior insula cortex, and posterior midcingulate cortex. Further, an interaction between inhibition and emotion was seen in valence-dependent variations in the quadratic trend in no-go activation in the right inferior frontal gyrus and left posterior insula cortex. These results suggest that the inhibition of response to emotional cues involves the interaction of partly dissociable limbic and frontoparietal networks that encode emotional cues and use these cues to exert inhibitory control over the motor, attention, and sensory functions needed to perform the task, respectively.
Human Brain Mapping, in press
Socially appropriate behavior requires the concurrent inhibition of actions that are inappropriate in the context. This self-regulatory function requires an interaction of inhibitory and emotional processes that recruits brain regions beyond those engaged by either processes alone. In this study, we isolated brain activity associated with response inhibition and emotional processing in 24 healthy adults using event-related functional magnetic resonance imaging (fMRI) and a go/no-go task that independently manipulated the context preceding no-go trials (ie, number of go trials) and the valence (ie, happy, sad, and neutral) of the face stimuli used as trial cues. Parallel quadratic trends were seen in correct inhibitions on no-go trials preceded by increasing numbers of go trials and associated activation for correct no-go trials in inferior frontal gyrus pars opercularis, pars triangularis, and pars orbitalis, temporoparietal junction, superior parietal lobule, and temporal sensory association cortices. Conversely, the comparison of happy versus neutral faces and sad versus neutral faces revealed valence-dependent activation in the amygdala, anterior insula cortex, and posterior midcingulate cortex. Further, an interaction between inhibition and emotion was seen in valence-dependent variations in the quadratic trend in no-go activation in the right inferior frontal gyrus and left posterior insula cortex. These results suggest that the inhibition of response to emotional cues involves the interaction of partly dissociable limbic and frontoparietal networks that encode emotional cues and use these cues to exert inhibitory control over the motor, attention, and sensory functions needed to perform the task, respectively.
Saturday, December 06, 2008
ARTICLE UPDATE - Working memory capacity and the self-regulation of emotional expression and experience.
Schmeichel BJ, Volokhov RN, Demaree HA.
Journal of Personality and Social Psychology, 95, 1526-1540
This research examined the relationship between individual differences in working memory capacity and the self-regulation of emotional expression and emotional experience. Four studies revealed that people higher in working memory capacity suppressed expressions of negative emotion (Study 1) and positive emotion (Study 2) better than did people lower in working memory capacity. Furthermore, compared to people lower in working memory capacity, people higher in capacity more capably appraised emotional stimuli in an unemotional manner and thereby experienced (Studies 3 and 4) and expressed (Study 4) less emotion in response to those stimuli. These findings indicate that cognitive ability contributes to the control of emotional responding.
Journal of Personality and Social Psychology, 95, 1526-1540
This research examined the relationship between individual differences in working memory capacity and the self-regulation of emotional expression and emotional experience. Four studies revealed that people higher in working memory capacity suppressed expressions of negative emotion (Study 1) and positive emotion (Study 2) better than did people lower in working memory capacity. Furthermore, compared to people lower in working memory capacity, people higher in capacity more capably appraised emotional stimuli in an unemotional manner and thereby experienced (Studies 3 and 4) and expressed (Study 4) less emotion in response to those stimuli. These findings indicate that cognitive ability contributes to the control of emotional responding.
ARTICLE UPDATE - Emotions in Go/NoGo conflicts.
Schacht A, Nigbur R, Sommer W.
Psychological Research, in press
On the basis of current emotion theories and functional and neurophysiological ties between the processing of conflicts and errors on the one hand and errors and emotions on the other hand we predicted that conflicts between prepotent Go responses and occasional NoGo trials in the Go/NoGo task would induce emotions. Skin conductance responses (SCRs), corrugator muscle activity, and startle blink responses were measured in three experiments requiring speeded Go responses intermixed with NoGo trials of different relative probability and in a choice reaction experiment serving as a control. NoGo trials affected several of these emotion-sensitive indicators as SCRs and startle blinks were reduced whereas corrugator activity was prolonged as compared to Go trials. From the pattern of findings we suggest that NoGo conflicts are not aversive. Instead, they appear to be appraised as obstructive for the response goal and as less action relevant than Go trials.
Psychological Research, in press
On the basis of current emotion theories and functional and neurophysiological ties between the processing of conflicts and errors on the one hand and errors and emotions on the other hand we predicted that conflicts between prepotent Go responses and occasional NoGo trials in the Go/NoGo task would induce emotions. Skin conductance responses (SCRs), corrugator muscle activity, and startle blink responses were measured in three experiments requiring speeded Go responses intermixed with NoGo trials of different relative probability and in a choice reaction experiment serving as a control. NoGo trials affected several of these emotion-sensitive indicators as SCRs and startle blinks were reduced whereas corrugator activity was prolonged as compared to Go trials. From the pattern of findings we suggest that NoGo conflicts are not aversive. Instead, they appear to be appraised as obstructive for the response goal and as less action relevant than Go trials.
ARTICLE UPDATE - Visual Awareness, Emotion, and Gamma Band Synchronization.
Luo Q, Mitchell D, Cheng X, Mondillo K, McCaffrey D, Holroyd T, Carver F, Coppola R, Blair J.
Cerebral Cortex, in press
What makes us become aware? A popular hypothesis is that if cortical neurons fire in synchrony at a certain frequency band (gamma), we become aware of what they are representing. We tested this hypothesis adopting brain-imaging techniques with good spatiotemporal resolution and frequency-specific information. Specifically, we examined the degree to which increases in event-related synchronization (ERS) in the gamma band were associated with awareness of a stimulus (its detectability) and/or the emotional content of the stimulus. We observed increases in gamma band ERS within prefrontal-anterior cingulate, visual, parietal, posterior cingulate, and superior temporal cortices to stimuli available to conscious awareness. However, we also observed increases in gamma band ERS within the amygdala, visual, prefrontal, parietal, and posterior cingulate cortices to emotional relative to neutral stimuli, irrespective of their availability to conscious access. This suggests that increased gamma band ERS is related to, but not sufficient for, consciousness.
Cerebral Cortex, in press
What makes us become aware? A popular hypothesis is that if cortical neurons fire in synchrony at a certain frequency band (gamma), we become aware of what they are representing. We tested this hypothesis adopting brain-imaging techniques with good spatiotemporal resolution and frequency-specific information. Specifically, we examined the degree to which increases in event-related synchronization (ERS) in the gamma band were associated with awareness of a stimulus (its detectability) and/or the emotional content of the stimulus. We observed increases in gamma band ERS within prefrontal-anterior cingulate, visual, parietal, posterior cingulate, and superior temporal cortices to stimuli available to conscious awareness. However, we also observed increases in gamma band ERS within the amygdala, visual, prefrontal, parietal, and posterior cingulate cortices to emotional relative to neutral stimuli, irrespective of their availability to conscious access. This suggests that increased gamma band ERS is related to, but not sufficient for, consciousness.
ARTICLE UPDATE - Attentional selectivity for emotional faces: Evidence from human electrophysiology.
Holmes A, Bradley BP, Kragh Nielsen M, Mogg K.
Psychophysiology, in press
Abstract This study investigated the temporal course of attentional biases for threat-related (angry) and positive (happy) facial expressions. Electrophysiological (event-related potential) and behavioral (reaction time [RT]) data were recorded while participants viewed pairs of faces (e.g., angry face paired with neutral face) shown for 500 ms and followed by a probe. Behavioral results indicated that RTs were faster to probes replacing emotional versus neutral faces, consistent with an attentional bias for emotional information. Electrophysiological results revealed that attentional orienting to threatening faces emerged earlier (early N2pc time window; 180-250 ms) than orienting to positive faces (after 250 ms), and that attention was sustained toward emotional faces during the 250-500-ms time window (late N2pc and SPCN components). These findings are consistent with models of attention and emotion that posit rapid attentional prioritization of threat.
Psychophysiology, in press
Abstract This study investigated the temporal course of attentional biases for threat-related (angry) and positive (happy) facial expressions. Electrophysiological (event-related potential) and behavioral (reaction time [RT]) data were recorded while participants viewed pairs of faces (e.g., angry face paired with neutral face) shown for 500 ms and followed by a probe. Behavioral results indicated that RTs were faster to probes replacing emotional versus neutral faces, consistent with an attentional bias for emotional information. Electrophysiological results revealed that attentional orienting to threatening faces emerged earlier (early N2pc time window; 180-250 ms) than orienting to positive faces (after 250 ms), and that attention was sustained toward emotional faces during the 250-500-ms time window (late N2pc and SPCN components). These findings are consistent with models of attention and emotion that posit rapid attentional prioritization of threat.
Saturday, November 22, 2008
ARTICLE UPDATE - See no evil: Directing visual attention within unpleasant images modulates the electrocortical response.
Dunning JP, Hajcak G.
Psychophysiology, in press
The late positive potential (LPP) is larger for emotional than neutral stimuli, and reflects increased attention to motivationally salient stimuli. Recent studies have shown that the LPP can also be modulated by stimulus meaning and task relevance. The present studies sought to determine whether the magnitude of the LPP can be manipulated by directing attention to more or less arousing aspects within an emotional stimulus. To this end, trials included a passive viewing and directed attention portion. In both Studies 1 and 2, unpleasant compared to neutral images were associated with an increased LPP during passive viewing; additionally, directing attention to non-arousing compared to highly arousing areas of unpleasant images resulted in a decreased LPP. Results are discussed in terms of the utility of using the LPP to understand emotion-cognition interactions, especially with regard to directed visual attention as an emotion regulation strategy.
Psychophysiology, in press
The late positive potential (LPP) is larger for emotional than neutral stimuli, and reflects increased attention to motivationally salient stimuli. Recent studies have shown that the LPP can also be modulated by stimulus meaning and task relevance. The present studies sought to determine whether the magnitude of the LPP can be manipulated by directing attention to more or less arousing aspects within an emotional stimulus. To this end, trials included a passive viewing and directed attention portion. In both Studies 1 and 2, unpleasant compared to neutral images were associated with an increased LPP during passive viewing; additionally, directing attention to non-arousing compared to highly arousing areas of unpleasant images resulted in a decreased LPP. Results are discussed in terms of the utility of using the LPP to understand emotion-cognition interactions, especially with regard to directed visual attention as an emotion regulation strategy.
ARTICLE UPDATE - Electrophysiological correlates of decreasing and increasing emotional responses to unpleasant pictures.
Moser JS, Krompinger JW, Dietz J, Simons RF.
Psychophysiology, in press
We examined event-related brain potential (ERP) modulations during the anticipation and processing of unpleasant pictures under instructions to cognitively decrease and increase negative emotion. Instructions to decrease and increase negative emotion modulated the ERP response to unpleasant pictures in the direction of emotional intensity beginning around 400 ms and lasting several seconds. Decrease, but not increase, instructions also elicited enhanced frontal negativity associated with orienting and preparation prior to unpleasant picture onset. Last, ERP modulation by unpleasant pictures began around 300 ms, just prior to regulation effects, suggesting that appraisal of emotion occurs before emotion regulation. Together, the current findings underscore the utility of ERPs in illuminating the time course of emotion modulation and regulation that may help to refine extant theoretical models.
Psychophysiology, in press
We examined event-related brain potential (ERP) modulations during the anticipation and processing of unpleasant pictures under instructions to cognitively decrease and increase negative emotion. Instructions to decrease and increase negative emotion modulated the ERP response to unpleasant pictures in the direction of emotional intensity beginning around 400 ms and lasting several seconds. Decrease, but not increase, instructions also elicited enhanced frontal negativity associated with orienting and preparation prior to unpleasant picture onset. Last, ERP modulation by unpleasant pictures began around 300 ms, just prior to regulation effects, suggesting that appraisal of emotion occurs before emotion regulation. Together, the current findings underscore the utility of ERPs in illuminating the time course of emotion modulation and regulation that may help to refine extant theoretical models.
ARTICLE UPDATE - Stereotype threat and executive resource depletion: Examining the influence of emotion regulation.
Johns M, Inzlicht M, Schmader T.
Journal of Experimental Psychology: General, 137, 691-705
Research shows that stereotype threat reduces performance by diminishing executive resources, but less is known about the psychological processes responsible for these impairments. The authors tested the idea that targets of stereotype threat try to regulate their emotions and that this regulation depletes executive resources, resulting in underperformance. Across 4 experiments, they provide converging evidence that targets of stereotype threat spontaneously attempt to control their expression of anxiety and that such emotion regulation depletes executive resources needed to perform well on tests of cognitive ability. They also demonstrate that providing threatened individuals with a means to effectively cope with negative emotions--by reappraising the situation or the meaning of their anxiety--can restore executive resources and improve test performance. They discuss these results within the framework of an integrated process model of stereotype threat, in which affective and cognitive processes interact to undermine performance.
Journal of Experimental Psychology: General, 137, 691-705
Research shows that stereotype threat reduces performance by diminishing executive resources, but less is known about the psychological processes responsible for these impairments. The authors tested the idea that targets of stereotype threat try to regulate their emotions and that this regulation depletes executive resources, resulting in underperformance. Across 4 experiments, they provide converging evidence that targets of stereotype threat spontaneously attempt to control their expression of anxiety and that such emotion regulation depletes executive resources needed to perform well on tests of cognitive ability. They also demonstrate that providing threatened individuals with a means to effectively cope with negative emotions--by reappraising the situation or the meaning of their anxiety--can restore executive resources and improve test performance. They discuss these results within the framework of an integrated process model of stereotype threat, in which affective and cognitive processes interact to undermine performance.
ARTICLE UPDATE - Validation of affective and neutral sentence content for prosodic testing.
Russ JB, Gur RC, Bilker WB.
Behavior Research Methods, 40,935-939
Conducting a study of emotional prosody often requires that one have a valid set of stimuli for assessing perceived emotion in vocal intonation. In this study, we created a list of sentences with both affective and neutral content, and then validated them against rater opinion. Participants read sentences with content that implied happiness, sadness, anger, fear, or neutrality and rated how well they could imagine each sentence being expressed in each emotion. Coefficients of variation and intraclass correlations were calculated to narrow the list to affective sentences that had high agreement and neutral sentences that had low agreement. We found that raters could easily identify most emotional content and did not ascribe any unique emotion to most neutral content. We also found differences between the intensity of male and female ratings. The final list of sentences is available on the Internet (www.med.upenn.edu/bbl/) and can be recorded for use as stimuli for prosodic studies.
Behavior Research Methods, 40,935-939
Conducting a study of emotional prosody often requires that one have a valid set of stimuli for assessing perceived emotion in vocal intonation. In this study, we created a list of sentences with both affective and neutral content, and then validated them against rater opinion. Participants read sentences with content that implied happiness, sadness, anger, fear, or neutrality and rated how well they could imagine each sentence being expressed in each emotion. Coefficients of variation and intraclass correlations were calculated to narrow the list to affective sentences that had high agreement and neutral sentences that had low agreement. We found that raters could easily identify most emotional content and did not ascribe any unique emotion to most neutral content. We also found differences between the intensity of male and female ratings. The final list of sentences is available on the Internet (www.med.upenn.edu/bbl/) and can be recorded for use as stimuli for prosodic studies.
ARTICLE UPDATE - Exploring the motivational brain: effects of implicit power motivation on brain activation in response to facial expressions of emoti
Schultheiss OC, Wirth MM, Waugh CE, Stanton SJ, Meier EA, Reuter-Lorenz P.
Social, Cognitive, Affective Neuroscience, in press
This study tested the hypothesis that implicit power motivation (nPower), in interaction with power incentives, influences activation of brain systems mediating motivation. Twelve individuals low (lowest quartile) and 12 individuals high (highest quartile) in nPower, as assessed per content coding of picture stories, were selected from a larger initial participant pool and participated in a functional magnetic resonance imaging study during which they viewed high-dominance (angry faces), low-dominance (surprised faces) and control stimuli (neutral faces, gray squares) under oddball-task conditions. Consistent with hypotheses, high-power participants showed stronger activation in response to emotional faces in brain structures involved in emotion and motivation (insula, dorsal striatum, orbitofrontal cortex) than low-power participants.
Social, Cognitive, Affective Neuroscience, in press
This study tested the hypothesis that implicit power motivation (nPower), in interaction with power incentives, influences activation of brain systems mediating motivation. Twelve individuals low (lowest quartile) and 12 individuals high (highest quartile) in nPower, as assessed per content coding of picture stories, were selected from a larger initial participant pool and participated in a functional magnetic resonance imaging study during which they viewed high-dominance (angry faces), low-dominance (surprised faces) and control stimuli (neutral faces, gray squares) under oddball-task conditions. Consistent with hypotheses, high-power participants showed stronger activation in response to emotional faces in brain structures involved in emotion and motivation (insula, dorsal striatum, orbitofrontal cortex) than low-power participants.
ARTICLE UPDATE - Rapid influence of emotional scenes on encoding of facial expressions: an ERP study.
Righart R, de Gelder B.
Social, Cognitive, Affective Neuroscience, 3, 270-278
In daily life, we perceive a person's facial reaction as part of the natural environment surrounding it. Because most studies have investigated how facial expressions are recognized by using isolated faces, it is unclear what role the context plays. Although it has been observed that the N170 for facial expressions is modulated by the emotional context, it was not clear whether individuals use context information on this stage of processing to discriminate between facial expressions. The aim of the present study was to investigate how the early stages of face processing are affected by emotional scenes when explicit categorizations of fearful and happy facial expressions are made. Emotion effects were found for the N170, with larger amplitudes for faces in fearful scenes as compared to faces in happy and neutral scenes. Critically, N170 amplitudes were significantly increased for fearful faces in fearful scenes as compared to fearful faces in happy scenes and expressed in left-occipito-temporal scalp topography differences. Our results show that the information provided by the facial expression is combined with the scene context during the early stages of face processing
Social, Cognitive, Affective Neuroscience, 3, 270-278
In daily life, we perceive a person's facial reaction as part of the natural environment surrounding it. Because most studies have investigated how facial expressions are recognized by using isolated faces, it is unclear what role the context plays. Although it has been observed that the N170 for facial expressions is modulated by the emotional context, it was not clear whether individuals use context information on this stage of processing to discriminate between facial expressions. The aim of the present study was to investigate how the early stages of face processing are affected by emotional scenes when explicit categorizations of fearful and happy facial expressions are made. Emotion effects were found for the N170, with larger amplitudes for faces in fearful scenes as compared to faces in happy and neutral scenes. Critically, N170 amplitudes were significantly increased for fearful faces in fearful scenes as compared to fearful faces in happy scenes and expressed in left-occipito-temporal scalp topography differences. Our results show that the information provided by the facial expression is combined with the scene context during the early stages of face processing
Sunday, November 09, 2008
ARTICLE UPDATE - Emotional modulation of visual and motor areas by dynamic body expressions of anger.
Pichon S, de Gelder B, Grezes J.
Social Neuroscience, 3, 199-212
The ability to detect emotional meaning in others' behavior constitutes a central component of social competence. Expressions of anger in particular present salient signals that play a major role in the regulation of social interactions. Investigations of human anger signals have to date used still pictures of facial expressions but so far the neurobiological basis of bodily communication of anger remains largely unknown. Using functional magnetic resonance imaging, the present study investigated the neural bases involved in perceiving anger signals emanating from the whole body. Our study also investigates what the presence of dynamic information adds to the perception of body expressions of anger. Participants were scanned while viewing stimuli (stills or videos) of angry and neutral whole-body expressions. Whole-body expressions of anger elicit activity in regions including the amygdala and the lateral orbitofrontal cortex, which play a role in the affective evaluation of the stimuli. Importantly, the perception of dynamic body expressions of anger additionally engages the hypothalamus, the ventromedial prefrontal cortex, the temporal pole and the premotor cortex, brain regions that are coupled with autonomic reactions and motor responses related to defensive behaviors.
Social Neuroscience, 3, 199-212
The ability to detect emotional meaning in others' behavior constitutes a central component of social competence. Expressions of anger in particular present salient signals that play a major role in the regulation of social interactions. Investigations of human anger signals have to date used still pictures of facial expressions but so far the neurobiological basis of bodily communication of anger remains largely unknown. Using functional magnetic resonance imaging, the present study investigated the neural bases involved in perceiving anger signals emanating from the whole body. Our study also investigates what the presence of dynamic information adds to the perception of body expressions of anger. Participants were scanned while viewing stimuli (stills or videos) of angry and neutral whole-body expressions. Whole-body expressions of anger elicit activity in regions including the amygdala and the lateral orbitofrontal cortex, which play a role in the affective evaluation of the stimuli. Importantly, the perception of dynamic body expressions of anger additionally engages the hypothalamus, the ventromedial prefrontal cortex, the temporal pole and the premotor cortex, brain regions that are coupled with autonomic reactions and motor responses related to defensive behaviors.
ARTICLE UPDATE - Effective connectivity between amygdala and orbitofrontal cortex differentiates the perception of facial expressions.
Liang X, Zebrowitz LA, Aharon I.
Social Neuroscience, in press
Emotion research is guided both by the view that emotions are points in a dimensional space, such as valence or approach-withdrawal, and by the view that emotions are discrete categories. We determined whether effective connectivity of amygdala with medial orbitofrontal cortex (MOFC) and lateral orbitofrontal cortex (LOFC) differentiates the perception of emotion faces in a manner consistent with the dimensional and/or categorical view. Greater effective connectivity from left MOFC to amygdala differentiated positive and neutral expressions from negatively valenced angry, disgust, and fear expressions. Greater effective connectivity from right LOFC to amygdala differentiated emotion expressions conducive to perceiver approach (happy, neutral, and fear) from angry expressions that elicit perceiver withdrawal. Finally, consistent with the categorical view, there were unique patterns of connectivity in response to fear, anger, and disgust, although not in response to happy expressions, which did not differ from neutral ones.
Social Neuroscience, in press
Emotion research is guided both by the view that emotions are points in a dimensional space, such as valence or approach-withdrawal, and by the view that emotions are discrete categories. We determined whether effective connectivity of amygdala with medial orbitofrontal cortex (MOFC) and lateral orbitofrontal cortex (LOFC) differentiates the perception of emotion faces in a manner consistent with the dimensional and/or categorical view. Greater effective connectivity from left MOFC to amygdala differentiated positive and neutral expressions from negatively valenced angry, disgust, and fear expressions. Greater effective connectivity from right LOFC to amygdala differentiated emotion expressions conducive to perceiver approach (happy, neutral, and fear) from angry expressions that elicit perceiver withdrawal. Finally, consistent with the categorical view, there were unique patterns of connectivity in response to fear, anger, and disgust, although not in response to happy expressions, which did not differ from neutral ones.
Sunday, November 02, 2008
ARTICLE UPDATE - Both predator and prey: emotional arousal in threat and reward.
Löw A, Lang PJ, Smith JC, Bradley MM.
Psychological Science, 19, 865-873
This research examined the psychophysiology of emotional arousal anticipatory to potentially aversive and highly pleasant outcomes. Human brain reactions (event-related potentials) and body reactions (heart rate, skin conductance, the probe startle reflex) were assessed along motivational gradients determined by apparent distance from sites of potential punishment or reward. A predator-prey survival context was simulated using cues that signaled possible money rewards or possible losses; the cues appeared to loom progressively closer to the viewer, until a final step when a rapid key response could ensure reward or avoid a punishing loss. The observed anticipatory response patterns of heightened vigilance and physiological mobilization are consistent with the view that the physiology of emotion is founded on action dispositions that evolved in mammals to facilitate survival by dealing with threats or capturing life-sustaining rewards.
Psychological Science, 19, 865-873
This research examined the psychophysiology of emotional arousal anticipatory to potentially aversive and highly pleasant outcomes. Human brain reactions (event-related potentials) and body reactions (heart rate, skin conductance, the probe startle reflex) were assessed along motivational gradients determined by apparent distance from sites of potential punishment or reward. A predator-prey survival context was simulated using cues that signaled possible money rewards or possible losses; the cues appeared to loom progressively closer to the viewer, until a final step when a rapid key response could ensure reward or avoid a punishing loss. The observed anticipatory response patterns of heightened vigilance and physiological mobilization are consistent with the view that the physiology of emotion is founded on action dispositions that evolved in mammals to facilitate survival by dealing with threats or capturing life-sustaining rewards.
ARTICLE UPDATE - Constructing emotion: the experience of fear as a conceptual act.
Lindquist KA, Barrett LF.
Psychological Science, 19, 898-903
This study examined the hypothesis that emotion is a psychological event constructed from the more basic elements of core affect and conceptual knowledge. Participants were primed with conceptual knowledge of fear, conceptual knowledge of anger, or a neutral prime and then proceeded through an affect-induction procedure designed to induce unpleasant, high-arousal affect or a neutral affective state. As predicted, only those individuals for whom conceptual knowledge of fear had been primed experienced unpleasant core affect as evidence that the world was threatening. This study provides the first experimental support for the hypothesis that people experience world-focused emotion when they conceptualize their core affective state using accessible knowledge about emotion.
Psychological Science, 19, 898-903
This study examined the hypothesis that emotion is a psychological event constructed from the more basic elements of core affect and conceptual knowledge. Participants were primed with conceptual knowledge of fear, conceptual knowledge of anger, or a neutral prime and then proceeded through an affect-induction procedure designed to induce unpleasant, high-arousal affect or a neutral affective state. As predicted, only those individuals for whom conceptual knowledge of fear had been primed experienced unpleasant core affect as evidence that the world was threatening. This study provides the first experimental support for the hypothesis that people experience world-focused emotion when they conceptualize their core affective state using accessible knowledge about emotion.
ARTICLE UPDATE - How does negative emotion cause false memories?
Brainerd CJ, Stein LM, Silveira RA, Rohenkohl G, Reyna VF.
Psychological Science, 19, 919-925
Remembering negative events can stimulate high levels of false memory, relative to remembering neutral events. In experiments in which the emotional valence of encoded materials was manipulated with their arousal levels controlled, valence produced a continuum of memory falsification. Falsification was highest for negative materials, intermediate for neutral materials, and lowest for positive materials. Conjoint-recognition analysis produced a simple process-level explanation: As one progresses from positive to neutral to negative valence, false memory increases because (a) the perceived meaning resemblance between false and true items increases and (b) subjects are less able to use verbatim memories of true items to suppress errors.
Psychological Science, 19, 919-925
Remembering negative events can stimulate high levels of false memory, relative to remembering neutral events. In experiments in which the emotional valence of encoded materials was manipulated with their arousal levels controlled, valence produced a continuum of memory falsification. Falsification was highest for negative materials, intermediate for neutral materials, and lowest for positive materials. Conjoint-recognition analysis produced a simple process-level explanation: As one progresses from positive to neutral to negative valence, false memory increases because (a) the perceived meaning resemblance between false and true items increases and (b) subjects are less able to use verbatim memories of true items to suppress errors.
ARTICLE UPDATE - Attention, emotion, and deactivation of default activity in inferior medial prefrontal cortex.
Geday J, Gjedde A.
Brain and Cognition, in press
Attention deactivates the inferior medial prefrontal cortex (IMPC), but it is uncertain if emotions can attenuate this deactivation. To test the extent to which common emotions interfere with attention, we measured changes of a blood flow index of brain activity in key areas of the IMPC with positron emission tomography (PET) of labeled water (H(2)(15)O) uptake in brain of 14 healthy subjects. The subjects performed either a less demanding or a more demanding task of attention while they watched neutral and emotive images of people in realistic indoor or outdoor situations. In the less demanding task, subjects used the index finger to press any key when a new image appeared. In the more demanding task, subjects chose the index or middle finger to press separate keys for outdoor and indoor scenes. Compared to the less demanding task, in a global search of all gray matter, the more demanding significantly lowered blood flow (rCBF) in left IMPC, left and right insula, and right amygdala, and significantly raised blood flow in motor cortex and right precuneus. Restricted searches of rCBF changes by emotion, at coordinates of significant effect in previous studies of the medial prefrontal and temporal cortices, revealed significant activation in the fusiform gyrus, independently of the task. In contrast, we found no effect of emotional content in the IMPC, where emotions failed to override the effect of the task. The results are consistent with a role of the IMPC in the selection among competitive inputs from multiple brain regions, as predicted by the theory of a default mode of brain function. The absent emotional interference with the deactivation of the default state suggests that the inferior prefrontal cortex continued to serve the attention rather than submit to the distraction.
Brain and Cognition, in press
Attention deactivates the inferior medial prefrontal cortex (IMPC), but it is uncertain if emotions can attenuate this deactivation. To test the extent to which common emotions interfere with attention, we measured changes of a blood flow index of brain activity in key areas of the IMPC with positron emission tomography (PET) of labeled water (H(2)(15)O) uptake in brain of 14 healthy subjects. The subjects performed either a less demanding or a more demanding task of attention while they watched neutral and emotive images of people in realistic indoor or outdoor situations. In the less demanding task, subjects used the index finger to press any key when a new image appeared. In the more demanding task, subjects chose the index or middle finger to press separate keys for outdoor and indoor scenes. Compared to the less demanding task, in a global search of all gray matter, the more demanding significantly lowered blood flow (rCBF) in left IMPC, left and right insula, and right amygdala, and significantly raised blood flow in motor cortex and right precuneus. Restricted searches of rCBF changes by emotion, at coordinates of significant effect in previous studies of the medial prefrontal and temporal cortices, revealed significant activation in the fusiform gyrus, independently of the task. In contrast, we found no effect of emotional content in the IMPC, where emotions failed to override the effect of the task. The results are consistent with a role of the IMPC in the selection among competitive inputs from multiple brain regions, as predicted by the theory of a default mode of brain function. The absent emotional interference with the deactivation of the default state suggests that the inferior prefrontal cortex continued to serve the attention rather than submit to the distraction.
Monday, October 20, 2008
ARTICLE UPDATE - Emotion Modulates Early Auditory Response to Speech.
Wang J, Nicol T, Skoe E, Sams M, Kraus N.
Journal of Cognitive Neuroscience, in press
In order to understand how emotional state influences the listener's physiological response to speech, subjects looked at emotion-evoking pictures while 32-channel EEG evoked responses (ERPs) to an unchanging auditory stimulus ("danny") were collected. The pictures were selected from the International Affective Picture System database. They were rated by participants and differed in valence (positive, negative, neutral), but not in dominance and arousal. Effects of viewing negative emotion pictures were seen as early as 20 msec (p = .006). An analysis of the global field power highlighted a time period of interest (30.4-129.0 msec) where the effects of emotion are likely to be the most robust. At the cortical level, the responses differed significantly depending on the valence ratings the subjects provided for the visual stimuli, which divided them into the high valence intensity group and the low valence intensity group. The high valence intensity group exhibited a clear divergent bivalent effect of emotion (ERPs at Cz during viewing neutral pictures subtracted from ERPs during viewing positive or negative pictures) in the time region of interest (r() = .534, p < .01). Moreover, group differences emerged in the pattern of global activation during this time period. Although both groups demonstrated a significant effect of emotion (ANOVA, p = .004 and .006, low valence intensity and high valence intensity, respectively), the high valence intensity group exhibited a much larger effect. Whereas the low valence intensity group exhibited its smaller effect predominantly in frontal areas, the larger effect in the high valence intensity group was found globally, especially in the left temporal areas, with the largest divergent bivalent effects (ANOVA, p < .00001) in high valence intensity subjects around the midline. Thus, divergent bivalent effects were observed between 30 and 130 msec, and were dependent on the subject's subjective state, whereas the effects at 20 msec were evident only for negative emotion, independent of the subject's behavioral responses. Taken together, it appears that emotion can affect auditory function early in the sensory processing stream.
Journal of Cognitive Neuroscience, in press
In order to understand how emotional state influences the listener's physiological response to speech, subjects looked at emotion-evoking pictures while 32-channel EEG evoked responses (ERPs) to an unchanging auditory stimulus ("danny") were collected. The pictures were selected from the International Affective Picture System database. They were rated by participants and differed in valence (positive, negative, neutral), but not in dominance and arousal. Effects of viewing negative emotion pictures were seen as early as 20 msec (p = .006). An analysis of the global field power highlighted a time period of interest (30.4-129.0 msec) where the effects of emotion are likely to be the most robust. At the cortical level, the responses differed significantly depending on the valence ratings the subjects provided for the visual stimuli, which divided them into the high valence intensity group and the low valence intensity group. The high valence intensity group exhibited a clear divergent bivalent effect of emotion (ERPs at Cz during viewing neutral pictures subtracted from ERPs during viewing positive or negative pictures) in the time region of interest (r() = .534, p < .01). Moreover, group differences emerged in the pattern of global activation during this time period. Although both groups demonstrated a significant effect of emotion (ANOVA, p = .004 and .006, low valence intensity and high valence intensity, respectively), the high valence intensity group exhibited a much larger effect. Whereas the low valence intensity group exhibited its smaller effect predominantly in frontal areas, the larger effect in the high valence intensity group was found globally, especially in the left temporal areas, with the largest divergent bivalent effects (ANOVA, p < .00001) in high valence intensity subjects around the midline. Thus, divergent bivalent effects were observed between 30 and 130 msec, and were dependent on the subject's subjective state, whereas the effects at 20 msec were evident only for negative emotion, independent of the subject's behavioral responses. Taken together, it appears that emotion can affect auditory function early in the sensory processing stream.
ARTICLE UPDATE - The valence strength of negative stimuli modulates visual novelty processing: Electrophysiological evidence from an event-related pot
Yuan J, Yang J, Meng X, Yu F, Li H.
Neuroscience, in press
In natural settings, the occurrence of unpredictable infrequent events is often associated with emotional reactions in the brain. Previous research suggested a special sensitivity of the brain to valence differences in emotionally negative stimuli. Thus, the present study hypothesizes that valence changes in infrequent negative stimuli would have differential effects on visual novelty processing. Event-related potentials (ERPs) were recorded for highly negative (HN), moderately negative (MN) and Neutral infrequent stimuli, and for the frequent standard stimulus while subjects performed a frequent/infrequent categorization task, irrespective of the emotional valence of the infrequent stimuli. The infrequent-frequent difference waves, which index visual novelty processing, displayed larger N2 amplitudes during HN condition than during MN condition which, in turn, elicited greater N2 amplitude than the Neutral condition. Similarly, in the infrequent-frequent difference waves, the frontocentral P3a and parietal LPC (late positive complex) elicited by the HN condition were more negative than those by MN stimuli, which elicited more negative amplitudes than the Neutral condition. This suggests that negative emotions of diverse strength, as induced by negative stimuli of varying valences, are clearly different in their impact on visual novelty processing. Novel stimuli of increased negativity elicited more attentional resources during the early novelty detection, and recruited increased inhibitive and evaluative processing during the later stages of response decision and reaction readiness, relative to novel stimuli of reduced negativity.
Neuroscience, in press
In natural settings, the occurrence of unpredictable infrequent events is often associated with emotional reactions in the brain. Previous research suggested a special sensitivity of the brain to valence differences in emotionally negative stimuli. Thus, the present study hypothesizes that valence changes in infrequent negative stimuli would have differential effects on visual novelty processing. Event-related potentials (ERPs) were recorded for highly negative (HN), moderately negative (MN) and Neutral infrequent stimuli, and for the frequent standard stimulus while subjects performed a frequent/infrequent categorization task, irrespective of the emotional valence of the infrequent stimuli. The infrequent-frequent difference waves, which index visual novelty processing, displayed larger N2 amplitudes during HN condition than during MN condition which, in turn, elicited greater N2 amplitude than the Neutral condition. Similarly, in the infrequent-frequent difference waves, the frontocentral P3a and parietal LPC (late positive complex) elicited by the HN condition were more negative than those by MN stimuli, which elicited more negative amplitudes than the Neutral condition. This suggests that negative emotions of diverse strength, as induced by negative stimuli of varying valences, are clearly different in their impact on visual novelty processing. Novel stimuli of increased negativity elicited more attentional resources during the early novelty detection, and recruited increased inhibitive and evaluative processing during the later stages of response decision and reaction readiness, relative to novel stimuli of reduced negativity.
ARTICLE UPDATE - The role of valence and frequency in the emotional Stroop task.
Kahan TA, Hely CD.
Psychological Bulletin & Review, 15, 956-960
People are generally slower to name the color of emotion-laden words than they are to name that of emotionally neutral words. However, an analysis of this emotional Stroop effect (Larsen, Mercer, & Balota, 2006) indicates that the emotion-laden words used are sometimes longer, have lower frequencies, and have smaller orthographic neighborhoods than the emotionally neutral words. This difference in word characteristics raises the possibility that the emotional Stroop effect is partly caused by lexical rather than by emotional aspects of the stimuli-a conclusion supported by the finding that reaction times to name the color of low-frequency words are longer than those for high-frequency words (Burt, 2002). To examine the relative contributions of valence and frequency in color naming, we had 64 participants complete an experiment in which each of these variables was manipulated in a 3 x 2 factorial design; length, orthographic neighborhood density, and arousal were balanced. The data indicate that valence and word frequency interact in contributing to the emotional Stroop effect.
Psychological Bulletin & Review, 15, 956-960
People are generally slower to name the color of emotion-laden words than they are to name that of emotionally neutral words. However, an analysis of this emotional Stroop effect (Larsen, Mercer, & Balota, 2006) indicates that the emotion-laden words used are sometimes longer, have lower frequencies, and have smaller orthographic neighborhoods than the emotionally neutral words. This difference in word characteristics raises the possibility that the emotional Stroop effect is partly caused by lexical rather than by emotional aspects of the stimuli-a conclusion supported by the finding that reaction times to name the color of low-frequency words are longer than those for high-frequency words (Burt, 2002). To examine the relative contributions of valence and frequency in color naming, we had 64 participants complete an experiment in which each of these variables was manipulated in a 3 x 2 factorial design; length, orthographic neighborhood density, and arousal were balanced. The data indicate that valence and word frequency interact in contributing to the emotional Stroop effect.
Wednesday, October 15, 2008
ARTICLE UPDATE - How Does Reward Expectation Influence Cognition in the Human Brain?
James B. Rowe, Doris Eckstein, Todd Braver and Adrian M. Owen
Journal of Cognitive Neuroscience,20, 1980-1992
The prospect of reward changes how we think and behave. We investigated how this occurs in the brain using a novel continuous performance task in which fluctuating reward expectations biased cognitive processes between competing spatial and verbal tasks. Critically, effects of reward expectancy could be distinguished from induced changes in task-related networks. Behavioral data confirm specific bias toward a reward-relevant modality. Increased reward expectation improves reaction time and accuracy in the relevant dimension while reducing sensitivity to modulations of stimuli characteristics in the irrelevant dimension. Analysis of functional magnetic resonance imaging data shows that the proximity to reward over successive trials is associated with increased activity of the medial frontal cortex regardless of the modality. However, there are modality-specific changes in brain activity in the lateral frontal, parietal, and temporal cortex. Analysis of effective connectivity suggests that reward expectancy enhances coupling in both early visual pathways and within the prefrontal cortex. These distributed changes in task-related cortical networks arise from subjects' representations of future events and likelihood of reward.
Journal of Cognitive Neuroscience,20, 1980-1992
The prospect of reward changes how we think and behave. We investigated how this occurs in the brain using a novel continuous performance task in which fluctuating reward expectations biased cognitive processes between competing spatial and verbal tasks. Critically, effects of reward expectancy could be distinguished from induced changes in task-related networks. Behavioral data confirm specific bias toward a reward-relevant modality. Increased reward expectation improves reaction time and accuracy in the relevant dimension while reducing sensitivity to modulations of stimuli characteristics in the irrelevant dimension. Analysis of functional magnetic resonance imaging data shows that the proximity to reward over successive trials is associated with increased activity of the medial frontal cortex regardless of the modality. However, there are modality-specific changes in brain activity in the lateral frontal, parietal, and temporal cortex. Analysis of effective connectivity suggests that reward expectancy enhances coupling in both early visual pathways and within the prefrontal cortex. These distributed changes in task-related cortical networks arise from subjects' representations of future events and likelihood of reward.
Saturday, October 11, 2008
ARTICLE UPDATE - Fear relevancy, strategy use, and probabilistic learning of cue-outcome associations.
Thomas LA, LaBar KS.
Learning & Memory, 15, 777-784
The goal of this study was to determine how the fear relevancy of outcomes during probabilistic classification learning affects behavior and strategy use. Novel variants of the "weather prediction" task were created, in which cue cards predicted either looming fearful or neutral outcomes in a between-groups design. Strategy use was examined by goodness-of-fit estimates of response patterns across trial blocks to mathematical models of simple, complex, and nonidentifiable strategies. Participants in the emotional condition who were fearful of the outcomes had greater skin conductance responses compared with controls and performed worse, used suboptimal strategies, and had less insight into the predictive cue features during initial learning. In contrast, nonfearful participants in the emotional condition used more optimal strategies than the other groups by the end of the two training days. Results have implications for understanding how individual differences in fear relevancy alter the impact of emotion on feedback-based learning.
Learning & Memory, 15, 777-784
The goal of this study was to determine how the fear relevancy of outcomes during probabilistic classification learning affects behavior and strategy use. Novel variants of the "weather prediction" task were created, in which cue cards predicted either looming fearful or neutral outcomes in a between-groups design. Strategy use was examined by goodness-of-fit estimates of response patterns across trial blocks to mathematical models of simple, complex, and nonidentifiable strategies. Participants in the emotional condition who were fearful of the outcomes had greater skin conductance responses compared with controls and performed worse, used suboptimal strategies, and had less insight into the predictive cue features during initial learning. In contrast, nonfearful participants in the emotional condition used more optimal strategies than the other groups by the end of the two training days. Results have implications for understanding how individual differences in fear relevancy alter the impact of emotion on feedback-based learning.
ARTICLE UPDATE - Electrophysiological correlates of affective blindsight.
Gonzalez Andino SL, Grave de Peralta Menendez R, Khateb A, Landis T, Pegna AJ.
Neuroimage, in press
An EEG investigation was carried out in a patient with complete cortical blindness who presented affective blindsight, i.e. who performed above chance when asked to guess the emotional expressions on a series of faces. To uncover the electrophysiological mechanisms involved in this phenomenon we combined multivariate pattern recognition (MPR) with local field potential estimates provided by electric source imaging (ELECTRA). All faces, including neutral faces, elicited distinctive oscillatory EEG patterns that were correctly identified by the MPR algorithm as belonging to the class of facial expressions actually presented. Consequently, neural responses in this patient are not restricted to emotionally laden faces. Earliest non-specific differences between faces occur from 70 ms onwards in the superior temporal polysensory area (STP). Emotion-specific responses were found after 120 ms in the right anterior areas with right amygdala activation observed only later ( approximately 200 ms). Thus, affective blindsight might be mediated by subcortical afferents to temporal areas as suggested in some studies involving non-emotional stimuli. The early activation of the STP in the patient constitutes evidence for fast activation of higher order visual areas in humans despite bilateral V1 destruction. In addition, the absence of awareness of any visual experience in this patient suggests that neither the extrastriate visual areas, nor the prefrontal cortex activation alone are sufficient for conscious perception, which might require recurrent processing within a network of several cerebral areas including V1.
Neuroimage, in press
An EEG investigation was carried out in a patient with complete cortical blindness who presented affective blindsight, i.e. who performed above chance when asked to guess the emotional expressions on a series of faces. To uncover the electrophysiological mechanisms involved in this phenomenon we combined multivariate pattern recognition (MPR) with local field potential estimates provided by electric source imaging (ELECTRA). All faces, including neutral faces, elicited distinctive oscillatory EEG patterns that were correctly identified by the MPR algorithm as belonging to the class of facial expressions actually presented. Consequently, neural responses in this patient are not restricted to emotionally laden faces. Earliest non-specific differences between faces occur from 70 ms onwards in the superior temporal polysensory area (STP). Emotion-specific responses were found after 120 ms in the right anterior areas with right amygdala activation observed only later ( approximately 200 ms). Thus, affective blindsight might be mediated by subcortical afferents to temporal areas as suggested in some studies involving non-emotional stimuli. The early activation of the STP in the patient constitutes evidence for fast activation of higher order visual areas in humans despite bilateral V1 destruction. In addition, the absence of awareness of any visual experience in this patient suggests that neither the extrastriate visual areas, nor the prefrontal cortex activation alone are sufficient for conscious perception, which might require recurrent processing within a network of several cerebral areas including V1.
ARTICLE UPDATE - The combined effect of gaze direction and facial expression on cueing spatial attention.
Pecchinenda A, Pes M, Ferlazzo F, Zoccolotti P.
Emotion, 8, 628-634
Empirical evidence shows an effect of gaze direction on cueing spatial attention, regardless of the emotional expression shown by a face, whereas a combined effect of gaze direction and facial expression has been observed on individuals' evaluative judgments. In 2 experiments, the authors investigated whether gaze direction and facial expression affect spatial attention depending upon the presence of an evaluative goal. Disgusted, fearful, happy, or neutral faces gazing left or right were followed by positive or negative target words presented either at the spatial location looked at by the face or at the opposite spatial location. Participants responded to target words based on affective valence (i.e., positive/negative) in Experiment 1 and on letter case (lowercase/uppercase) in Experiment 2. Results showed that participants responded much faster to targets presented at the spatial location looked at by disgusted or fearful faces but only in Experiment 1, when an evaluative task was used. The present findings clearly show that negative facial expressions enhance the attentional shifts due to eye-gaze direction, provided that there was an explicit evaluative goal present.
Emotion, 8, 628-634
Empirical evidence shows an effect of gaze direction on cueing spatial attention, regardless of the emotional expression shown by a face, whereas a combined effect of gaze direction and facial expression has been observed on individuals' evaluative judgments. In 2 experiments, the authors investigated whether gaze direction and facial expression affect spatial attention depending upon the presence of an evaluative goal. Disgusted, fearful, happy, or neutral faces gazing left or right were followed by positive or negative target words presented either at the spatial location looked at by the face or at the opposite spatial location. Participants responded to target words based on affective valence (i.e., positive/negative) in Experiment 1 and on letter case (lowercase/uppercase) in Experiment 2. Results showed that participants responded much faster to targets presented at the spatial location looked at by disgusted or fearful faces but only in Experiment 1, when an evaluative task was used. The present findings clearly show that negative facial expressions enhance the attentional shifts due to eye-gaze direction, provided that there was an explicit evaluative goal present.
ARTICLE UPDATE - Directed forgetting of emotional words.
Minnema MT, Knowlton BJ.
Emotion, 8, 643-652
Emotional material may induce processing limitations affecting memory performance. In the present study, the authors investigated how the emotional content of words influences the degree to which participants can be directed to forget them. In Experiment 1, the authors found that negative-valence words were recalled better when participants were told to forget them than when they were told to remember them. This effect was only obtained when a study-list of negative words was presented after the cue to remember or forget the first list. The effect was correlated with negative mood as assessed by the PANAS. Similar results were obtained in Experiment 2, in which the induction of negative arousal by a mild stressor abolished the directed forgetting of words when the following study list was comprised of negative words. These results support the idea that directed forgetting relies on cognitive control processes that may be disrupted by negative emotion.
Emotion, 8, 643-652
Emotional material may induce processing limitations affecting memory performance. In the present study, the authors investigated how the emotional content of words influences the degree to which participants can be directed to forget them. In Experiment 1, the authors found that negative-valence words were recalled better when participants were told to forget them than when they were told to remember them. This effect was only obtained when a study-list of negative words was presented after the cue to remember or forget the first list. The effect was correlated with negative mood as assessed by the PANAS. Similar results were obtained in Experiment 2, in which the induction of negative arousal by a mild stressor abolished the directed forgetting of words when the following study list was comprised of negative words. These results support the idea that directed forgetting relies on cognitive control processes that may be disrupted by negative emotion.
ARTICLE UPDATE - Trouble crossing the bridge: Altered interhemispheric communication of emotional images in anxiety.
Compton RJ, Carp J, Chaddock L, Fineman SL, Quandt LC, Ratliff JB.
Emotion, 8, 684-692.
Worry is thought to involve a strategy of cognitive avoidance, in which internal verbalization acts to suppress threatening emotional imagery. This study tested the hypothesis that worry-prone individuals would exhibit patterns of between-hemisphere communication that reflect cognitive avoidance. Specifically, the hypothesis predicted slower transfer of threatening images from the left to the right hemisphere among worriers. Event-related potential (ERP) measures of interhemispheric transfer time supported this prediction. Left-to-right hemisphere transfer times for angry faces were relatively slower for individuals scoring high in self-reported worry compared with those scoring low, whereas transfer of happy and neutral faces did not differ between groups. These results suggest that altered interhemispheric communication may constitute one mechanism of cognitive avoidance in worry.
Emotion, 8, 684-692.
Worry is thought to involve a strategy of cognitive avoidance, in which internal verbalization acts to suppress threatening emotional imagery. This study tested the hypothesis that worry-prone individuals would exhibit patterns of between-hemisphere communication that reflect cognitive avoidance. Specifically, the hypothesis predicted slower transfer of threatening images from the left to the right hemisphere among worriers. Event-related potential (ERP) measures of interhemispheric transfer time supported this prediction. Left-to-right hemisphere transfer times for angry faces were relatively slower for individuals scoring high in self-reported worry compared with those scoring low, whereas transfer of happy and neutral faces did not differ between groups. These results suggest that altered interhemispheric communication may constitute one mechanism of cognitive avoidance in worry.
ARTICLE UPDATE - Interpretation bias in social anxiety as detected by event-related brain potentials.
Moser JS, Hajcak G, Huppert JD, Foa EB, Simons RF.
Emotion, 8, 693-700
Little is known about psychophysiological correlates of interpretation bias in social anxiety. To address this issue, the authors measured event-related brain potentials (ERPs) in high and low socially anxious individuals during a task wherein ambiguous scenarios were resolved with either a positive or negative ending. Specifically, the authors examined modulations of the P600, an ERP that peaks approximately 600 ms following stimulus onset and indexes violations of expectancy. Low-anxious individuals were characterized by an increased P600 to negative in comparison with positive sentence endings, suggesting a positive interpretation bias. In contrast, the high-anxious group evidenced equivalent P600 magnitude for negative and positive sentence endings, suggesting a lack of positive interpretation bias. Similar, but less reliable results emerged in earlier time windows, that is, 200-500 ms poststimulus. Reaction time, occurring around 900 ms poststimulus, failed to show a reliable interpretation bias. Results suggest that ERPs can detect interpretation biases in social anxiety before the emission of behavioral responses.
Emotion, 8, 693-700
Little is known about psychophysiological correlates of interpretation bias in social anxiety. To address this issue, the authors measured event-related brain potentials (ERPs) in high and low socially anxious individuals during a task wherein ambiguous scenarios were resolved with either a positive or negative ending. Specifically, the authors examined modulations of the P600, an ERP that peaks approximately 600 ms following stimulus onset and indexes violations of expectancy. Low-anxious individuals were characterized by an increased P600 to negative in comparison with positive sentence endings, suggesting a positive interpretation bias. In contrast, the high-anxious group evidenced equivalent P600 magnitude for negative and positive sentence endings, suggesting a lack of positive interpretation bias. Similar, but less reliable results emerged in earlier time windows, that is, 200-500 ms poststimulus. Reaction time, occurring around 900 ms poststimulus, failed to show a reliable interpretation bias. Results suggest that ERPs can detect interpretation biases in social anxiety before the emission of behavioral responses.
Saturday, September 20, 2008
ARTICLE UPDATE - Is emotional contagion special? An fMRI study on neural systems for affective and cognitive empathy.
Nummenmaa L, Hirvonen J, Parkkola R, Hietanen JK.
Neuroimage, in press
Empathy allows us to simulate others' affective and cognitive mental states internally, and it has been proposed that the mirroring or motor representation systems play a key role in such simulation. As emotions are related to important adaptive events linked with benefit or danger, simulating others' emotional states might constitute of a special case of empathy. In this functional magnetic resonance imaging (fMRI) study we tested if emotional versus cognitive empathy would facilitate the recruitment of brain networks involved in motor representation and imitation in healthy volunteers. Participants were presented with photographs depicting people in neutral everyday situations (cognitive empathy blocks), or suffering serious threat or harm (emotional empathy blocks). Participants were instructed to empathize with specified persons depicted in the scenes. Emotional versus cognitive empathy resulted in increased activity in limbic areas involved in emotion processing (thalamus), and also in cortical areas involved in face (fusiform gyrus) and body (extrastriate cortex) perception, as well as in networks associated with mirroring of others' actions (inferior parietal lobule). When brain activation resulting from viewing the scenes was controlled, emotional empathy still engaged the mirror neuron system (premotor cortex) more than cognitive empathy. Further, thalamus and primary somatosensory and motor cortices showed increased functional coupling during emotional versus cognitive empathy. The results suggest that emotional empathy is special. Emotional empathy facilitates somatic, sensory, and motor representation of other peoples' mental states, and results in more vigorous mirroring of the observed mental and bodily states than cognitive empathy.
Neuroimage, in press
Empathy allows us to simulate others' affective and cognitive mental states internally, and it has been proposed that the mirroring or motor representation systems play a key role in such simulation. As emotions are related to important adaptive events linked with benefit or danger, simulating others' emotional states might constitute of a special case of empathy. In this functional magnetic resonance imaging (fMRI) study we tested if emotional versus cognitive empathy would facilitate the recruitment of brain networks involved in motor representation and imitation in healthy volunteers. Participants were presented with photographs depicting people in neutral everyday situations (cognitive empathy blocks), or suffering serious threat or harm (emotional empathy blocks). Participants were instructed to empathize with specified persons depicted in the scenes. Emotional versus cognitive empathy resulted in increased activity in limbic areas involved in emotion processing (thalamus), and also in cortical areas involved in face (fusiform gyrus) and body (extrastriate cortex) perception, as well as in networks associated with mirroring of others' actions (inferior parietal lobule). When brain activation resulting from viewing the scenes was controlled, emotional empathy still engaged the mirror neuron system (premotor cortex) more than cognitive empathy. Further, thalamus and primary somatosensory and motor cortices showed increased functional coupling during emotional versus cognitive empathy. The results suggest that emotional empathy is special. Emotional empathy facilitates somatic, sensory, and motor representation of other peoples' mental states, and results in more vigorous mirroring of the observed mental and bodily states than cognitive empathy.
Sunday, September 14, 2008
ARTICLE UPDATE - The human amygdala is involved in general behavioral relevance detection: Evidence from an event-related functional magnetic resonanc
Ousdal OT, Jensen J, Server A, Hariri AR, Nakstad PH, Andreassen OA.
Neuroscience, in press
The amygdala is classically regarded as a detector of potential threat and as a critical component of the neural circuitry mediating conditioned fear responses. However, it has been reported that the human amygdala responds to multiple expressions of emotions as well as emotionally neutral stimuli of a novel, uncertain or ambiguous nature. Thus, it has been proposed that the function of the amygdala may be of a more general art, i.e. as a detector of behaviorally relevant stimuli [Sander D, Grafman J, Zalla T (2003) The human amygdala: an evolved system for relevance detection. Rev Neurosci 14:303-316]. To investigate this putative function of the amygdala, we used event related functional magnetic resonance imaging (fMRI) and a modified Go-NoGo task composed of behaviorally relevant and irrelevant letter and number stimuli. Analyses revealed bilateral amygdala activation in response to letter stimuli that were behaviorally relevant as compared with letters with less behavioral relevance. Similar results were obtained for relatively infrequent NoGo relevant stimuli as compared with more frequent Go stimuli. Our findings support a role for the human amygdala in general detection of behaviorally relevant stimuli.
Neuroscience, in press
The amygdala is classically regarded as a detector of potential threat and as a critical component of the neural circuitry mediating conditioned fear responses. However, it has been reported that the human amygdala responds to multiple expressions of emotions as well as emotionally neutral stimuli of a novel, uncertain or ambiguous nature. Thus, it has been proposed that the function of the amygdala may be of a more general art, i.e. as a detector of behaviorally relevant stimuli [Sander D, Grafman J, Zalla T (2003) The human amygdala: an evolved system for relevance detection. Rev Neurosci 14:303-316]. To investigate this putative function of the amygdala, we used event related functional magnetic resonance imaging (fMRI) and a modified Go-NoGo task composed of behaviorally relevant and irrelevant letter and number stimuli. Analyses revealed bilateral amygdala activation in response to letter stimuli that were behaviorally relevant as compared with letters with less behavioral relevance. Similar results were obtained for relatively infrequent NoGo relevant stimuli as compared with more frequent Go stimuli. Our findings support a role for the human amygdala in general detection of behaviorally relevant stimuli.
ARTICLE UPDATE - Natural selective attention: Orienting and emotion.
Bradley MM.
Psychophysiology, in press
The foundations of orienting and attention are hypothesized to stem from activation of defensive and appetitive motivational systems that evolved to protect and sustain the life of the individual. Motivational activation initiates a cascade of perceptual and motor processes that facilitate the selection of appropriate behavior. Among these are detection of significance, indexed by a late centro-parietal positivity in the event-related potential, enhanced perceptual processing, indexed by a initial cardiac deceleration, and preparation for action, indexed by electrodermal changes. Data exploring the role of stimulus novelty and significance in orienting are presented that indicate different components of the orienting response habituate at different rates. Taken together, it is suggested that orienting is mediated by activation of fundamental motivational systems that have evolved to support survival.
Psychophysiology, in press
The foundations of orienting and attention are hypothesized to stem from activation of defensive and appetitive motivational systems that evolved to protect and sustain the life of the individual. Motivational activation initiates a cascade of perceptual and motor processes that facilitate the selection of appropriate behavior. Among these are detection of significance, indexed by a late centro-parietal positivity in the event-related potential, enhanced perceptual processing, indexed by a initial cardiac deceleration, and preparation for action, indexed by electrodermal changes. Data exploring the role of stimulus novelty and significance in orienting are presented that indicate different components of the orienting response habituate at different rates. Taken together, it is suggested that orienting is mediated by activation of fundamental motivational systems that have evolved to support survival.
ARTICLE UPDATE - Neural Circuitry Underlying the Regulation of Conditioned Fear and Its Relation to Extinction.
Delgado MR, Nearing KI, Ledoux JE, Phelps EA.
Neuron, 59, 829-838
Recent efforts to translate basic research to the treatment of clinical disorders have led to a growing interest in exploring mechanisms for diminishing fear. This research has emphasized two approaches: extinction of conditioned fear, examined across species; and cognitive emotion regulation, unique to humans. Here, we sought to examine the similarities and differences in the neural mechanisms underlying these two paradigms for diminishing fear. Using an emotion regulation strategy, we examine the neural mechanisms of regulating conditioned fear using fMRI and compare the resulting activation pattern with that observed during classic extinction. Our results suggest that the lateral PFC regions engaged by cognitive emotion regulation strategies may influence the amygdala, diminishing fear through similar vmPFC connections that are thought to inhibit the amygdala during extinction. These findings further suggest that humans may have developed complex cognition that can aid in regulating emotional responses while utilizing phylogenetically shared mechanisms of extinction.
Neuron, 59, 829-838
Recent efforts to translate basic research to the treatment of clinical disorders have led to a growing interest in exploring mechanisms for diminishing fear. This research has emphasized two approaches: extinction of conditioned fear, examined across species; and cognitive emotion regulation, unique to humans. Here, we sought to examine the similarities and differences in the neural mechanisms underlying these two paradigms for diminishing fear. Using an emotion regulation strategy, we examine the neural mechanisms of regulating conditioned fear using fMRI and compare the resulting activation pattern with that observed during classic extinction. Our results suggest that the lateral PFC regions engaged by cognitive emotion regulation strategies may influence the amygdala, diminishing fear through similar vmPFC connections that are thought to inhibit the amygdala during extinction. These findings further suggest that humans may have developed complex cognition that can aid in regulating emotional responses while utilizing phylogenetically shared mechanisms of extinction.
ARTICLE UPDATE - Mapping the Semantic Space for the Subjective Experience of Emotional Responses to Odors.
Chrea C, Grandjean D, Delplanque S, Cayeux I, Le Calvé B, Aymard L, Velazco MI, Sander D, Scherer KR.
Chemical Senses, in press
Two studies were conducted to examine the nature of the verbal labels that describe emotional effects elicited by odors. In Study 1, a list of terms selected for their relevance to describe affective feelings induced by odors was assessed while participants were exposed to a set of odorant samples. The data were submitted to a series of exploratory factor analyses to 1) reduce the set of variables to a smaller set of summary scales and 2) get a preliminary sense of the differentiation of affective feelings elicited by odors. The goal of Study 2 was to replicate the findings of Study 1 with a larger sample of odorant samples and participants and to validate the preliminary model obtained in Study 1 by using confirmatory factor analysis. Overall, the findings point to a structure of affective responses to odors that differs from the classical taxonomies of emotion such as posited by discrete or bidimensional emotion theories. These findings suggest that the subjective affective experiences or feelings induced by odors are structured around a small group of dimensions that reflect the role of olfaction in well-being, social interaction, danger prevention, arousal or relaxation sensations, and conscious recollection of emotional memories.
Chemical Senses, in press
Two studies were conducted to examine the nature of the verbal labels that describe emotional effects elicited by odors. In Study 1, a list of terms selected for their relevance to describe affective feelings induced by odors was assessed while participants were exposed to a set of odorant samples. The data were submitted to a series of exploratory factor analyses to 1) reduce the set of variables to a smaller set of summary scales and 2) get a preliminary sense of the differentiation of affective feelings elicited by odors. The goal of Study 2 was to replicate the findings of Study 1 with a larger sample of odorant samples and participants and to validate the preliminary model obtained in Study 1 by using confirmatory factor analysis. Overall, the findings point to a structure of affective responses to odors that differs from the classical taxonomies of emotion such as posited by discrete or bidimensional emotion theories. These findings suggest that the subjective affective experiences or feelings induced by odors are structured around a small group of dimensions that reflect the role of olfaction in well-being, social interaction, danger prevention, arousal or relaxation sensations, and conscious recollection of emotional memories.
Sunday, September 07, 2008
ARTICLE UPDATE - Music-induced mood modulates the strength of emotional negativity bias: An ERP study.
Chen J, Yuan J, Huang H, Chen C, Li H.
Neuroscience Letters, in press,
The present study investigated the effect of music-elicited moods on the subsequent affective processing through a music-primed valence categorization task. Event-related potentials were recorded for positive and negative emotional pictures that were primed by happy or sad music excerpts. The reaction time data revealed longer reaction times (RTs) for pictures following negative versus positive music pieces, irrespective of the valence of the picture. Additionally, positive pictures elicited faster response latencies than negative pictures, irrespective of the valence of the musical prime. Moreover, the main effect of picture valence, and the music by picture valence interaction effect were both significant for P2 amplitudes and for the averaged amplitudes at 500-700ms interval. Negative pictures elicited smaller P2 amplitudes than positive pictures, and the amplitude differences between negative and positive pictures were larger with negative musical primes than with positive musical primes. Similarly, compared to positive pictures, negative pictures elicited more negative deflections during the 500-700ms interval across prime types. The amplitude differences between negative and positive pictures were again larger under negative versus positive music primes at this interval. Therefore, the present study observed a clear emotional negativity bias during either prime condition, and extended the previous findings by showing increased strength of the negative bias under negative mood primes. This suggests that the neural sensitivity of the brain to negative stimuli varies with individuals' mood states, and this bias is particularly intensified by negative mood states.
Neuroscience Letters, in press,
The present study investigated the effect of music-elicited moods on the subsequent affective processing through a music-primed valence categorization task. Event-related potentials were recorded for positive and negative emotional pictures that were primed by happy or sad music excerpts. The reaction time data revealed longer reaction times (RTs) for pictures following negative versus positive music pieces, irrespective of the valence of the picture. Additionally, positive pictures elicited faster response latencies than negative pictures, irrespective of the valence of the musical prime. Moreover, the main effect of picture valence, and the music by picture valence interaction effect were both significant for P2 amplitudes and for the averaged amplitudes at 500-700ms interval. Negative pictures elicited smaller P2 amplitudes than positive pictures, and the amplitude differences between negative and positive pictures were larger with negative musical primes than with positive musical primes. Similarly, compared to positive pictures, negative pictures elicited more negative deflections during the 500-700ms interval across prime types. The amplitude differences between negative and positive pictures were again larger under negative versus positive music primes at this interval. Therefore, the present study observed a clear emotional negativity bias during either prime condition, and extended the previous findings by showing increased strength of the negative bias under negative mood primes. This suggests that the neural sensitivity of the brain to negative stimuli varies with individuals' mood states, and this bias is particularly intensified by negative mood states.
Monday, September 01, 2008
ARTICLE UPDATE - Visual search for faces with emotional expressions.
Frischen A, Eastwood JD, Smilek D.
Psychological Bulletin, 134, 662-676
The goal of this review is to critically examine contradictory findings in the study of visual search for emotionally expressive faces. Several key issues are addressed: Can emotional faces be processed preattentively and guide attention? What properties of these faces influence search efficiency? Is search moderated by the emotional state of the observer? The authors argue that the evidence is consistent with claims that (a) preattentive search processes are sensitive to and influenced by facial expressions of emotion, (b) attention guidance is influenced by a dynamic interplay of emotional and perceptual factors, and (c) visual search for emotional faces is influenced by the emotional state of the observer to some extent. The authors also argue that the way in which contextual factors interact to determine search performance needs to be explored further to draw sound conclusions about the precise influence of emotional expressions on search efficiency. Methodological considerations (e.g., set size, distractor background, task set) and ecological limitations of the visual search task are discussed. Finally, specific recommendations are made for future research directions.
Psychological Bulletin, 134, 662-676
The goal of this review is to critically examine contradictory findings in the study of visual search for emotionally expressive faces. Several key issues are addressed: Can emotional faces be processed preattentively and guide attention? What properties of these faces influence search efficiency? Is search moderated by the emotional state of the observer? The authors argue that the evidence is consistent with claims that (a) preattentive search processes are sensitive to and influenced by facial expressions of emotion, (b) attention guidance is influenced by a dynamic interplay of emotional and perceptual factors, and (c) visual search for emotional faces is influenced by the emotional state of the observer to some extent. The authors also argue that the way in which contextual factors interact to determine search performance needs to be explored further to draw sound conclusions about the precise influence of emotional expressions on search efficiency. Methodological considerations (e.g., set size, distractor background, task set) and ecological limitations of the visual search task are discussed. Finally, specific recommendations are made for future research directions.
ARTICLE UPDATE - Individual differences in learning the affective value of others under minimal conditions.
Bliss-Moreau E, Barrett LF, Wright CI.
Emotion, 8, 479-493.
This paper provides the first demonstration that people can learn about the positive and negative value of other people (e.g., neutral faces) under minimal learning conditions, with stable individual differences in this learning. In four studies, participants viewed neutral faces paired with sentences describing positive, negative or neutral behaviors on either two (Study 1) or four (Studies 2, 3, and 4) occasions. Participants were later asked to judge the valence of the faces alone. Studies 1 and 2 demonstrated that learning does occur under minimal conditions. Study 3 and 4 further demonstrated that the degree of learning was moderated by Extraversion. Finally, Study 4 demonstrated that initial learning persisted over a period of 2 days. Implications for affective processing and person perception are discussed.
Emotion, 8, 479-493.
This paper provides the first demonstration that people can learn about the positive and negative value of other people (e.g., neutral faces) under minimal learning conditions, with stable individual differences in this learning. In four studies, participants viewed neutral faces paired with sentences describing positive, negative or neutral behaviors on either two (Study 1) or four (Studies 2, 3, and 4) occasions. Participants were later asked to judge the valence of the faces alone. Studies 1 and 2 demonstrated that learning does occur under minimal conditions. Study 3 and 4 further demonstrated that the degree of learning was moderated by Extraversion. Finally, Study 4 demonstrated that initial learning persisted over a period of 2 days. Implications for affective processing and person perception are discussed.
ARTICLE UPDATE - Emotion Theory and Research: Highlights, Unanswered Questions, and Emerging Issues.
Izard CE.
Annual Review of Psychology, in press
Emotion feeling is a phase of neurobiological activity, the key component of emotions and emotion-cognition interactions. Emotion schemas, the most frequently occurring emotion experiences, are dynamic emotion-cognition interactions that may consist of momentary/ situational responding or enduring traits of personality that emerge over developmental time. Emotions play a critical role in the evolution of consciousness and the operations of all mental processes. Types of emotion relate differentially to types or levels of consciousness. Unbridled imagination and the ability for sympathetic regulation of empathy may represent both potential gains and losses from the evolution and ontogeny of emotion processes and consciousness. Unresolved issues include psychology’s neglect of levels of consciousness that are distinct from access or reflective consciousness and use of the term “unconscious mind” as a dumpster for all mental processes that are considered unreportable. The relation of memes and the mirror neuron system to empathy, sympathy, and cultural influences on the development of socioemotional skills are unresolved issues destined to attract future research.
Annual Review of Psychology, in press
Emotion feeling is a phase of neurobiological activity, the key component of emotions and emotion-cognition interactions. Emotion schemas, the most frequently occurring emotion experiences, are dynamic emotion-cognition interactions that may consist of momentary/ situational responding or enduring traits of personality that emerge over developmental time. Emotions play a critical role in the evolution of consciousness and the operations of all mental processes. Types of emotion relate differentially to types or levels of consciousness. Unbridled imagination and the ability for sympathetic regulation of empathy may represent both potential gains and losses from the evolution and ontogeny of emotion processes and consciousness. Unresolved issues include psychology’s neglect of levels of consciousness that are distinct from access or reflective consciousness and use of the term “unconscious mind” as a dumpster for all mental processes that are considered unreportable. The relation of memes and the mirror neuron system to empathy, sympathy, and cultural influences on the development of socioemotional skills are unresolved issues destined to attract future research.
ARTICLE UPDATE - Differential Influences of Emotion, Task, and Novelty on Brain Regions Underlying the Processing of Speech Melody.
Ethofer T, Kreifelts B, Wiethoff S, Wolf J, Grodd W, Vuilleumier P, Wildgruber D.
The Journal of Cognitive Neuroscience, in press
Abstract We investigated the functional characteristics of brain regions implicated in processing of speech melody by presenting words spoken in either neutral or angry prosody during a functional magnetic resonance imaging experiment using a factorial habituation design. Subjects judged either affective prosody or word class for these vocal stimuli, which could be heard for either the first, second, or third time. Voice-sensitive temporal cortices, as well as the amygdala, insula, and mediodorsal thalami, reacted stronger to angry than to neutral prosody. These stimulus-driven effects were not influenced by the task, suggesting that these brain structures are automatically engaged during processing of emotional information in the voice and operate relatively independent of cognitive demands. By contrast, the right middle temporal gyrus and the bilateral orbito-frontal cortices (OFC) responded stronger during emotion than word classification, but were also sensitive to anger expressed by the voices, suggesting that some perceptual aspects of prosody are also encoded within these regions subserving explicit processing of vocal emotion. The bilateral OFC showed a selective modulation by emotion and repetition, with particularly pronounced responses to angry prosody during the first presentation only, indicating a critical role of the OFC in detection of vocal information that is both novel and behaviorally relevant. These results converge with previous findings obtained for angry faces and suggest a general involvement of the OFC for recognition of anger irrespective of the sensory modality. Taken together, our study reveals that different aspects of voice stimuli and perceptual demands modulate distinct areas involved in the processing of emotional prosody.
The Journal of Cognitive Neuroscience, in press
Abstract We investigated the functional characteristics of brain regions implicated in processing of speech melody by presenting words spoken in either neutral or angry prosody during a functional magnetic resonance imaging experiment using a factorial habituation design. Subjects judged either affective prosody or word class for these vocal stimuli, which could be heard for either the first, second, or third time. Voice-sensitive temporal cortices, as well as the amygdala, insula, and mediodorsal thalami, reacted stronger to angry than to neutral prosody. These stimulus-driven effects were not influenced by the task, suggesting that these brain structures are automatically engaged during processing of emotional information in the voice and operate relatively independent of cognitive demands. By contrast, the right middle temporal gyrus and the bilateral orbito-frontal cortices (OFC) responded stronger during emotion than word classification, but were also sensitive to anger expressed by the voices, suggesting that some perceptual aspects of prosody are also encoded within these regions subserving explicit processing of vocal emotion. The bilateral OFC showed a selective modulation by emotion and repetition, with particularly pronounced responses to angry prosody during the first presentation only, indicating a critical role of the OFC in detection of vocal information that is both novel and behaviorally relevant. These results converge with previous findings obtained for angry faces and suggest a general involvement of the OFC for recognition of anger irrespective of the sensory modality. Taken together, our study reveals that different aspects of voice stimuli and perceptual demands modulate distinct areas involved in the processing of emotional prosody.
Sunday, August 24, 2008
ARTICLE UPDATE - Affective valence, stimulus attributes, and P300: Color vs. black/white and normal vs. scrambled images.
Cano ME, Class QA, Polich J.
International Journal of Psychophysiology, in press
Pictures from the International Affective Picture System (IAPS) were selected to manipulate affective valence (unpleasant, neutral, pleasant) while keeping arousal level the same. The pictures were presented in an oddball paradigm, with a visual pattern used as the standard stimulus. Subjects pressed a button whenever a target was detected. Experiment 1 presented normal pictures in color and black/white. Control stimuli were constructed for both the color and black/white conditions by randomly rearranging 1 cm square fragments of each original picture to produce a "scrambled" image. Experiment 2 presented the same normal color pictures with large, medium, and small scrambled condition (2, 1, and 0.5 cm squares). The P300 event-related brain potential demonstrated larger amplitudes over frontal areas for positive compared to negative or neutral images for normal color pictures in both experiments. Attenuated and nonsignificant valence effects were obtained for black/white images. Scrambled stimuli in each study yielded no valence effects but demonstrated typical P300 topography that increased from frontal to parietal areas. The findings suggest that P300 amplitude is sensitive to affective picture valence in the absence of stimulus arousal differences, and that stimulus color contributes to ERP valence effects.
International Journal of Psychophysiology, in press
Pictures from the International Affective Picture System (IAPS) were selected to manipulate affective valence (unpleasant, neutral, pleasant) while keeping arousal level the same. The pictures were presented in an oddball paradigm, with a visual pattern used as the standard stimulus. Subjects pressed a button whenever a target was detected. Experiment 1 presented normal pictures in color and black/white. Control stimuli were constructed for both the color and black/white conditions by randomly rearranging 1 cm square fragments of each original picture to produce a "scrambled" image. Experiment 2 presented the same normal color pictures with large, medium, and small scrambled condition (2, 1, and 0.5 cm squares). The P300 event-related brain potential demonstrated larger amplitudes over frontal areas for positive compared to negative or neutral images for normal color pictures in both experiments. Attenuated and nonsignificant valence effects were obtained for black/white images. Scrambled stimuli in each study yielded no valence effects but demonstrated typical P300 topography that increased from frontal to parietal areas. The findings suggest that P300 amplitude is sensitive to affective picture valence in the absence of stimulus arousal differences, and that stimulus color contributes to ERP valence effects.
ARTICLE UPDATE - Visual search is not blind to emotion.
Gerritsen C, Frischen A, Blake A, Smilek D, Eastwood JD.
Perception and Psychophysics, 70, 1047-1059
A series of three visual search tasks revealed more efficient search for hostile than for peaceful faces among neutral face distractors. Given that this effect has been observed inconsistently in prior literature, meta-analytic methods were employed for evaluating data across three experiments in order to develop a more valid estimate of the potentially small effect size. Furthermore, in the present experiments, different emotional meanings were conditioned to identical faces across observers, thus eliminating confounds between the physical characteristics and the emotional valences of the face stimuli. On the basis of the present findings, we argue that the visual system is capable of determining a face's emotional valence before the face becomes the focus of attention, and that emotional valence can be used by the visual system to determine subsequent attention allocation. However, meta-analytic results indicate that emotional valence makes a relatively small contribution to search efficiency in the present search context.
Perception and Psychophysics, 70, 1047-1059
A series of three visual search tasks revealed more efficient search for hostile than for peaceful faces among neutral face distractors. Given that this effect has been observed inconsistently in prior literature, meta-analytic methods were employed for evaluating data across three experiments in order to develop a more valid estimate of the potentially small effect size. Furthermore, in the present experiments, different emotional meanings were conditioned to identical faces across observers, thus eliminating confounds between the physical characteristics and the emotional valences of the face stimuli. On the basis of the present findings, we argue that the visual system is capable of determining a face's emotional valence before the face becomes the focus of attention, and that emotional valence can be used by the visual system to determine subsequent attention allocation. However, meta-analytic results indicate that emotional valence makes a relatively small contribution to search efficiency in the present search context.
Saturday, August 16, 2008
ARTICLE UPDATE - Integration of cross-modal emotional information in the human brain: An fMRI study.
Park JY, Gu BM, Kang DH, Shin YW, Choi CH, Lee JM, Kwon JS.
Cortex, in press
The interaction of information derived from the voice and facial expression of a speaker contributes to the interpretation of the emotional state of the speaker and to the formation of inferences about information that may have been merely implied in the verbal communication. Therefore, we investigated the brain processes responsible for the integration of emotional information originating from different sources. Although several studies have reported possible sites for integration, further investigation using a neutral emotional condition is required to locate emotion-specific networks. Using functional magnetic resonance imaging (fMRI), we explored the brain regions involved in the integration of emotional information from different modalities in comparison to those involved in integrating emotionally neutral information. There was significant activation in the superior temporal gyrus (STG); inferior frontal gyrus (IFG); and parahippocampal gyrus, including the amygdala, under the bimodal versus the unimodal condition, irrespective of the emotional content. We confirmed the results of previous studies by finding that the bimodal emotional condition elicited strong activation in the left middle temporal gyrus (MTG), and we extended this finding to locate the effects of emotional factors by using a neutral condition in the experimental design. We found anger-specific activation in the posterior cingulate, fusiform gyrus, and cerebellum, whereas we found happiness-specific activation in the MTG, parahippocampal gyrus, hippocampus, claustrum, inferior parietal lobule, cuneus, middle frontal gyrus (MFG), IFG, and anterior cingulate. These emotion-specific activations suggest that each emotion uses a separate network to integrate bimodal information and shares a common network for cross-modal integration.
Cortex, in press
The interaction of information derived from the voice and facial expression of a speaker contributes to the interpretation of the emotional state of the speaker and to the formation of inferences about information that may have been merely implied in the verbal communication. Therefore, we investigated the brain processes responsible for the integration of emotional information originating from different sources. Although several studies have reported possible sites for integration, further investigation using a neutral emotional condition is required to locate emotion-specific networks. Using functional magnetic resonance imaging (fMRI), we explored the brain regions involved in the integration of emotional information from different modalities in comparison to those involved in integrating emotionally neutral information. There was significant activation in the superior temporal gyrus (STG); inferior frontal gyrus (IFG); and parahippocampal gyrus, including the amygdala, under the bimodal versus the unimodal condition, irrespective of the emotional content. We confirmed the results of previous studies by finding that the bimodal emotional condition elicited strong activation in the left middle temporal gyrus (MTG), and we extended this finding to locate the effects of emotional factors by using a neutral condition in the experimental design. We found anger-specific activation in the posterior cingulate, fusiform gyrus, and cerebellum, whereas we found happiness-specific activation in the MTG, parahippocampal gyrus, hippocampus, claustrum, inferior parietal lobule, cuneus, middle frontal gyrus (MFG), IFG, and anterior cingulate. These emotion-specific activations suggest that each emotion uses a separate network to integrate bimodal information and shares a common network for cross-modal integration.
ARTICLE UPDATE - I feel how you feel but not always: the empathic brain and its modulation.
Hein G, Singer T.
Current Opinions in Neurobiology, in press
The ability to share the other's feelings, known as empathy, has recently become the focus of social neuroscience studies. We review converging evidence that empathy with, for example, the pain of another person, activates part of the neural pain network of the empathizer, without first hand pain stimulation to the empathizer's body. The amplitude of empathic brain responses is modulated by the intensity of the displayed emotion, the appraisal of the situation, characteristics of the suffering person such as perceived fairness, and features of the empathizer such as gender or previous experience with pain-inflicting situations. Future studies in the field should address inter-individual differences in empathy, development and plasticity of the empathic brain over the life span, and the link between empathy, compassionate motivation, and prosocial behavior.
Current Opinions in Neurobiology, in press
The ability to share the other's feelings, known as empathy, has recently become the focus of social neuroscience studies. We review converging evidence that empathy with, for example, the pain of another person, activates part of the neural pain network of the empathizer, without first hand pain stimulation to the empathizer's body. The amplitude of empathic brain responses is modulated by the intensity of the displayed emotion, the appraisal of the situation, characteristics of the suffering person such as perceived fairness, and features of the empathizer such as gender or previous experience with pain-inflicting situations. Future studies in the field should address inter-individual differences in empathy, development and plasticity of the empathic brain over the life span, and the link between empathy, compassionate motivation, and prosocial behavior.
ARTICLE UPDATE - How emotional arousal and valence influence access to awareness.
Sheth BR, Pham T.
Vision Research, in press
Volume 8, Number 6, Abstract 248, Page 248a doi:10.1167/8.6.248 http://journalofvision.org/8/6/248/ ISSN 1534-7362
How emotional arousal and affect influence access to visual awareness
Bruno Breitmeyer
Department of Psychology, University of Houston, and Center for NeuroEngineering and Cognitive Science, University of Houston
[e-mail]
Thuan Pham
University of Houston
Bhavin Sheth
Department of Electrical and Computer Engineering, University of Houston, and Center for NeuroEngineering and Cognitive Science, University of Houston
Abstract
Emotional stimuli attract attention and potentiate the effect of attention on contrast sensitivity, a feature of early vision. The amygdala, a key structure in emotional processing, responds to emotional content prior to awareness and projects to visual cortex. In light of evidence that the primary visual cortex does not have direct access to awareness, we hypothesize that emotion can affect the processing of a visual stimulus even before awareness. Moreover, emotion varies along at least two dimensions: arousal and affect (valence). Dissociating their effects is important to understanding the link between emotion and perception. We examined these effects in binocular rivalry. Pairs of images (54 total) were selected from a known database of natural images (IAPS). Pictures of a pair differed significantly along only one emotional dimension, creating two types – iso-valence and iso-arousal pairs. Pictures of a given pair were presented side by side in a rivalry setup for trials lasting 1 min. each. The duration for which each eye's image was dominant in a trial (dominant phase duration) was obtained from 12 observers. Our results showed: –A main effect of arousal: The dominant phase durations for more arousing pictures of the iso-valence pairs were significantly longer than those for the less arousing pictures. –No main effect of affect: The dominant phase durations of pleasant and unpleasant pictures of iso-arousal pairs did not differ significantly. –An interaction between arousal and affect: For low arousal-level stimuli, the more pleasant image of the pair dominated significantly. In contrast, for high arousal-level stimuli, the more unpleasant image dominated significantly. Our findings suggest that the limbic system acts on visual signals early in processing. While emotional arousal and valence interactively affect access to visual awareness, only arousal exerts an independent control of such access.
Vision Research, in press
Volume 8, Number 6, Abstract 248, Page 248a doi:10.1167/8.6.248 http://journalofvision.org/8/6/248/ ISSN 1534-7362
How emotional arousal and affect influence access to visual awareness
Bruno Breitmeyer
Department of Psychology, University of Houston, and Center for NeuroEngineering and Cognitive Science, University of Houston
[e-mail]
Thuan Pham
University of Houston
Bhavin Sheth
Department of Electrical and Computer Engineering, University of Houston, and Center for NeuroEngineering and Cognitive Science, University of Houston
Abstract
Emotional stimuli attract attention and potentiate the effect of attention on contrast sensitivity, a feature of early vision. The amygdala, a key structure in emotional processing, responds to emotional content prior to awareness and projects to visual cortex. In light of evidence that the primary visual cortex does not have direct access to awareness, we hypothesize that emotion can affect the processing of a visual stimulus even before awareness. Moreover, emotion varies along at least two dimensions: arousal and affect (valence). Dissociating their effects is important to understanding the link between emotion and perception. We examined these effects in binocular rivalry. Pairs of images (54 total) were selected from a known database of natural images (IAPS). Pictures of a pair differed significantly along only one emotional dimension, creating two types – iso-valence and iso-arousal pairs. Pictures of a given pair were presented side by side in a rivalry setup for trials lasting 1 min. each. The duration for which each eye's image was dominant in a trial (dominant phase duration) was obtained from 12 observers. Our results showed: –A main effect of arousal: The dominant phase durations for more arousing pictures of the iso-valence pairs were significantly longer than those for the less arousing pictures. –No main effect of affect: The dominant phase durations of pleasant and unpleasant pictures of iso-arousal pairs did not differ significantly. –An interaction between arousal and affect: For low arousal-level stimuli, the more pleasant image of the pair dominated significantly. In contrast, for high arousal-level stimuli, the more unpleasant image dominated significantly. Our findings suggest that the limbic system acts on visual signals early in processing. While emotional arousal and valence interactively affect access to visual awareness, only arousal exerts an independent control of such access.
ARTICLE UPDATE - A common anterior insula representation of disgust observation, experience and imagination shows divergent functional connectivity pa
Jabbi M, Bastiaansen J, Keysers C.
PLoS
Similar brain regions are involved when we imagine, observe and execute an action. Is the same true for emotions? Here, the same subjects were scanned while they (a) experience, (b) view someone else experiencing and (c) imagine experiencing gustatory emotions (through script-driven imagery). Capitalizing on the fact that disgust is repeatedly inducible within the scanner environment, we scanned the same participants while they (a) view actors taste the content of a cup and look disgusted (b) tasted unpleasant bitter liquids to induce disgust, and (c) read and imagine scenarios involving disgust and their neutral counterparts. To reduce habituation, we inter-mixed trials of positive emotions in all three scanning experiments. We found voxels in the anterior Insula and adjacent frontal operculum to be involved in all three modalities of disgust, suggesting that simulation in the context of social perception and mental imagery of disgust share a common neural substrates. Using effective connectivity, this shared region however was found to be embedded in distinct functional circuits during the three modalities, suggesting why observing, imagining and experiencing an emotion feels so different
PLoS
Similar brain regions are involved when we imagine, observe and execute an action. Is the same true for emotions? Here, the same subjects were scanned while they (a) experience, (b) view someone else experiencing and (c) imagine experiencing gustatory emotions (through script-driven imagery). Capitalizing on the fact that disgust is repeatedly inducible within the scanner environment, we scanned the same participants while they (a) view actors taste the content of a cup and look disgusted (b) tasted unpleasant bitter liquids to induce disgust, and (c) read and imagine scenarios involving disgust and their neutral counterparts. To reduce habituation, we inter-mixed trials of positive emotions in all three scanning experiments. We found voxels in the anterior Insula and adjacent frontal operculum to be involved in all three modalities of disgust, suggesting that simulation in the context of social perception and mental imagery of disgust share a common neural substrates. Using effective connectivity, this shared region however was found to be embedded in distinct functional circuits during the three modalities, suggesting why observing, imagining and experiencing an emotion feels so different
Wednesday, August 13, 2008
ARTICLE UPDATE - The human amygdala is sensitive to the valence of pictures and sounds irrespective of arousal: an fMRI study
Silke Anders, Falk Eippert, Nikolaus Weiskopf and Ralf Veit
Social Cognitive and Affective Neuroscience, in press
With the advent of studies showing that amygdala responses are not limited to fear-related or highly unpleasant stimuli, studies began to focus on stimulus valence and stimulus-related arousal as predictors of amygdala activity. Recent studies in the chemosensory domain found amygdala activity to increase with the intensity of negative and positive chemosensory stimuli. This has led to the proposal that amygdala activity might be an indicator of emotional arousal, at least in the chemosensory domain. The present study investigated amygdala activity in response to visual and auditory stimuli. By selecting stimuli based on individual valence and arousal ratings, we were able to dissociate stimulus valence and stimulus-related arousal, both on the verbal and the peripheral physiological level. We found that the amygdala was sensitive to stimulus valence even when arousal was controlled for, and that increased amygdala activity was better explained by valence than by arousal. The proposed difference in the relation between amygdala activity and stimulus-related arousal between the chemosensory and the audiovisual domain is discussed in terms of the amygdala's embedding within these sensory systems and the processes by which emotional meaning is derived.
Social Cognitive and Affective Neuroscience, in press
With the advent of studies showing that amygdala responses are not limited to fear-related or highly unpleasant stimuli, studies began to focus on stimulus valence and stimulus-related arousal as predictors of amygdala activity. Recent studies in the chemosensory domain found amygdala activity to increase with the intensity of negative and positive chemosensory stimuli. This has led to the proposal that amygdala activity might be an indicator of emotional arousal, at least in the chemosensory domain. The present study investigated amygdala activity in response to visual and auditory stimuli. By selecting stimuli based on individual valence and arousal ratings, we were able to dissociate stimulus valence and stimulus-related arousal, both on the verbal and the peripheral physiological level. We found that the amygdala was sensitive to stimulus valence even when arousal was controlled for, and that increased amygdala activity was better explained by valence than by arousal. The proposed difference in the relation between amygdala activity and stimulus-related arousal between the chemosensory and the audiovisual domain is discussed in terms of the amygdala's embedding within these sensory systems and the processes by which emotional meaning is derived.
Saturday, August 09, 2008
ARTICLE UPDATE - Emotional experience modulates brain activity during fixation periods between tasks.Emotional experience modulates brain activity dur
Pitroda S, Angstadt M, McCloskey MS, Coccaro EF, Phan KL.
Neuroscience Letters, in press
Functional imaging studies have begun to identify a set of brain regions whose brain activity is greater during 'rest' (e.g., fixation) states than during cognitive tasks. It has been posited that these regions constitute a network that supports the brain's default mode, which is temporarily suspended during specific goal-directed behaviors. Exogenous tasks that require cognitive effort are thought to command reallocation of resources away from the brain's default state. However, it remains unknown if brain activity during fixation periods between active task periods is influenced by previous task-related emotional content. We examined brain activity during periods of FIXATION (viewing and rating gray-scale images) interspersed among periods of viewing and rating complex images ('PICTURE') with positive, negative, and neutral affective content. We show that a selected group of brain regions (PCC, precuneus, IPL, vACC) do exhibit activity that is greater during FIXATION (>PICTURE); these regions have previously been implicated in the "default brain network". In addition, we report that activity within precuneus and IPL in the FIXATION period is attenuated by the precedent processing of images with positive and negative emotional content, relative to non-emotional content. These data suggest that the activity within regions implicated in the default network is modulated by the presence of environmental stimuli with motivational salience and, thus, adds to our understanding of the brain function during periods of low cognitive, emotional, or sensory demand.
Neuroscience Letters, in press
Functional imaging studies have begun to identify a set of brain regions whose brain activity is greater during 'rest' (e.g., fixation) states than during cognitive tasks. It has been posited that these regions constitute a network that supports the brain's default mode, which is temporarily suspended during specific goal-directed behaviors. Exogenous tasks that require cognitive effort are thought to command reallocation of resources away from the brain's default state. However, it remains unknown if brain activity during fixation periods between active task periods is influenced by previous task-related emotional content. We examined brain activity during periods of FIXATION (viewing and rating gray-scale images) interspersed among periods of viewing and rating complex images ('PICTURE') with positive, negative, and neutral affective content. We show that a selected group of brain regions (PCC, precuneus, IPL, vACC) do exhibit activity that is greater during FIXATION (>PICTURE); these regions have previously been implicated in the "default brain network". In addition, we report that activity within precuneus and IPL in the FIXATION period is attenuated by the precedent processing of images with positive and negative emotional content, relative to non-emotional content. These data suggest that the activity within regions implicated in the default network is modulated by the presence of environmental stimuli with motivational salience and, thus, adds to our understanding of the brain function during periods of low cognitive, emotional, or sensory demand.
ARTICLE UPDATE - Functional neuroimaging of reward processing and decision-making: A review of aberrant motivational and affective processing in addic
Diekhof EK, Falkai P, Gruber O.
Brain Research Review, in press
The adequate integration of reward- and decision-related information provided by the environment is critical for behavioral success and subjective well being in everyday life. Functional neuroimaging research has already presented a comprehensive picture on affective and motivational processing in the healthy human brain and has recently also turned its interest to the assessment of impaired brain function in psychiatric patients. This article presents an overview on neuroimaging studies dealing with reward processing and decision-making by combining most recent findings from fundamental and clinical research. It provides an outline on the neural mechanisms guiding context-adequate reward processing and decision-making processes in the healthy brain, and also addresses pathophysiological alterations in the brain's reward system that have been observed in substance abuse and mood disorders, two highly prevalent classes of psychiatric disorders. The overall goal is to critically evaluate the specificity of neurophysiological alterations identified in these psychiatric disorders and associated symptoms, and to make suggestions concerning future research.
Brain Research Review, in press
The adequate integration of reward- and decision-related information provided by the environment is critical for behavioral success and subjective well being in everyday life. Functional neuroimaging research has already presented a comprehensive picture on affective and motivational processing in the healthy human brain and has recently also turned its interest to the assessment of impaired brain function in psychiatric patients. This article presents an overview on neuroimaging studies dealing with reward processing and decision-making by combining most recent findings from fundamental and clinical research. It provides an outline on the neural mechanisms guiding context-adequate reward processing and decision-making processes in the healthy brain, and also addresses pathophysiological alterations in the brain's reward system that have been observed in substance abuse and mood disorders, two highly prevalent classes of psychiatric disorders. The overall goal is to critically evaluate the specificity of neurophysiological alterations identified in these psychiatric disorders and associated symptoms, and to make suggestions concerning future research.
Saturday, August 02, 2008
ARTICLE UPDATE - The selective processing of emotional visual stimuli while detecting auditory targets: An ERP analysis.
Schupp HT, Stockburger J, Bublatzky F, Junghöfer M, Weike AI, Hamm AO.
Brain Research, in press
Event-related potential studies revealed an early posterior negativity (EPN) for emotional compared to neutral pictures. Exploring the emotion-attention relationship, a previous study observed that a primary visual discrimination task interfered with the emotional modulation of the EPN component. To specify the locus of interference, the present study assessed the fate of selective visual emotion processing while attention is directed towards the auditory modality. While simply viewing a rapid and continuous stream of pleasant, neutral, and unpleasant pictures in one experimental condition, processing demands of a concurrent auditory target discrimination task were systematically varied in three further experimental conditions. Participants successfully performed the auditory task as revealed by behavioral performance and selected event-related potential components. Replicating previous results, emotional pictures were associated with a larger posterior negativity compared to neutral pictures. Of main interest, increasing demands of the auditory task did not modulate the selective processing of emotional visual stimuli. With regard to the locus of interference, selective emotion processing as indexed by the EPN does not seem to reflect shared processing resources of visual and auditory modality.
Brain Research, in press
Event-related potential studies revealed an early posterior negativity (EPN) for emotional compared to neutral pictures. Exploring the emotion-attention relationship, a previous study observed that a primary visual discrimination task interfered with the emotional modulation of the EPN component. To specify the locus of interference, the present study assessed the fate of selective visual emotion processing while attention is directed towards the auditory modality. While simply viewing a rapid and continuous stream of pleasant, neutral, and unpleasant pictures in one experimental condition, processing demands of a concurrent auditory target discrimination task were systematically varied in three further experimental conditions. Participants successfully performed the auditory task as revealed by behavioral performance and selected event-related potential components. Replicating previous results, emotional pictures were associated with a larger posterior negativity compared to neutral pictures. Of main interest, increasing demands of the auditory task did not modulate the selective processing of emotional visual stimuli. With regard to the locus of interference, selective emotion processing as indexed by the EPN does not seem to reflect shared processing resources of visual and auditory modality.
ARTICLE UPDATE - Communicating emotion: Linking affective prosody and word meaning.
Nygaard LC, Queen JS.
Journal of Experimental Psychology: Human Perception & Performance, 34, 1017-1030
The present study investigated the role of emotional tone of voice in the perception of spoken words. Listeners were presented with words that had either a happy, sad, or neutral meaning. Each word was spoken in a tone of voice (happy, sad, or neutral) that was congruent, incongruent, or neutral with respect to affective meaning, and naming latencies were collected. Across experiments, tone of voice was either blocked or mixed with respect to emotional meaning. The results suggest that emotional tone of voice facilitated linguistic processing of emotional words in an emotion-congruent fashion. These findings suggest that information about emotional tone is used in the processing of linguistic content influencing the recognition and naming of spoken words in an emotion-congruent manner.
Journal of Experimental Psychology: Human Perception & Performance, 34, 1017-1030
The present study investigated the role of emotional tone of voice in the perception of spoken words. Listeners were presented with words that had either a happy, sad, or neutral meaning. Each word was spoken in a tone of voice (happy, sad, or neutral) that was congruent, incongruent, or neutral with respect to affective meaning, and naming latencies were collected. Across experiments, tone of voice was either blocked or mixed with respect to emotional meaning. The results suggest that emotional tone of voice facilitated linguistic processing of emotional words in an emotion-congruent fashion. These findings suggest that information about emotional tone is used in the processing of linguistic content influencing the recognition and naming of spoken words in an emotion-congruent manner.
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