Quirin M, Kazén M, Kuhl J.
Journal of Personality and Social Psychology, 97, 500-516
This article introduces an instrument for the indirect assessment of positive and negative affect, the Implicit Positive and Negative Affect Test (IPANAT). This test draws on participant ratings of the extent to which artificial words subjectively convey various emotions. Factor analyses of these ratings yielded two independent factors that can be interpreted as implicit positive and negative affect. The corresponding scales show adequate internal consistency, test-retest reliability, stability (Study 1), and construct validity (Study 2). Studies 3 and 4 demonstrate that the IPANAT also measures state variance. Finally, Study 5 provides criterion-based validity by demonstrating that correlations between implicit affect and explicit affect are higher under conditions of spontaneous responding than under conditions of reflective responding to explicit affect scales. The present findings suggest that the IPANAT is a reliable and valid measure with a straightforward application procedure.
This blog keeps you up-to-date with latest emotion related research. Feel free to browse and contribute.
Monday, August 24, 2009
ARTICLE UPDATE - Smile Through Your Fear and Sadness.
Smith FW, Schyns PG.
Psychological Science, in press
ABSTRACT- It is well established that animal communication signals have adapted to the evolutionary pressures of their environment. For example, the low-frequency vocalizations of the elephant are tailored to long-range communications, whereas the high-frequency trills of birds are adapted to their more localized acoustic niche. Like the voice, the human face transmits social signals about the internal emotional state of the transmitter. Here, we address two main issues: First, we characterized the spectral composition of the facial features signaling each of the six universal expressions of emotion (happiness, sadness, fear, disgust, anger, and surprise). From these analyses, we then predicted and tested the effectiveness of the transmission of emotion signals over different viewing distances. We reveal a gradient of recognition over viewing distances constraining the relative adaptive usefulness of facial expressions of emotion (distal expressions are good signals over a wide range of viewing distances; proximal expressions are suited to closer-range communication).
Psychological Science, in press
ABSTRACT- It is well established that animal communication signals have adapted to the evolutionary pressures of their environment. For example, the low-frequency vocalizations of the elephant are tailored to long-range communications, whereas the high-frequency trills of birds are adapted to their more localized acoustic niche. Like the voice, the human face transmits social signals about the internal emotional state of the transmitter. Here, we address two main issues: First, we characterized the spectral composition of the facial features signaling each of the six universal expressions of emotion (happiness, sadness, fear, disgust, anger, and surprise). From these analyses, we then predicted and tested the effectiveness of the transmission of emotion signals over different viewing distances. We reveal a gradient of recognition over viewing distances constraining the relative adaptive usefulness of facial expressions of emotion (distal expressions are good signals over a wide range of viewing distances; proximal expressions are suited to closer-range communication).
ARTICLE UPDATE - Response and habituation of the amygdala during processing of emotional prosody.
Wiethoff S, Wildgruber D, Grodd W, Ethofer T.
Neuroreport, in press
The role of the amygdala in processing acoustic information of affective value is still under debate. Using event-related functional MRI (fMRI), we showed increased amygdalar responses to various emotions (anger, fear, happiness, eroticism) expressed by prosody, a means of communication bound to language and consequently unique to humans. The smallest signal increases were found for fearful prosody, a finding that could not be explained by rapid response habituation to stimuli of this emotional category, challenging classical theories about fear specificity of the human amygdala. Our results converge with earlier neuroimaging evidence investigating emotional vocalizations, and these neurobiological similarities suggest that the two forms of communication might have common evolutionary roots.
Neuroreport, in press
The role of the amygdala in processing acoustic information of affective value is still under debate. Using event-related functional MRI (fMRI), we showed increased amygdalar responses to various emotions (anger, fear, happiness, eroticism) expressed by prosody, a means of communication bound to language and consequently unique to humans. The smallest signal increases were found for fearful prosody, a finding that could not be explained by rapid response habituation to stimuli of this emotional category, challenging classical theories about fear specificity of the human amygdala. Our results converge with earlier neuroimaging evidence investigating emotional vocalizations, and these neurobiological similarities suggest that the two forms of communication might have common evolutionary roots.
Monday, August 17, 2009
ARTICLE UPDATE - Distinct brain systems underlie the processing of valence and arousal of affective pictures.
Nielen MM, Heslenfeld DJ, Heinen K, Van Strien JW, Witter MP, Jonker C, Veltman DJ.
Brain & Cognition, in press
Valence and arousal are thought to be the primary dimensions of human emotion. However, the degree to which valence and arousal interact in determining brain responses to emotional pictures is still elusive. This functional MRI study aimed to delineate neural systems responding to valence and arousal, and their interaction. We measured neural activation in healthy females (N=23) to affective pictures using a 2 (Valence)x2 (Arousal) design. Results show that arousal was preferentially processed by middle temporal gyrus, hippocampus and ventrolateral prefrontal cortex. Regions responding to negative valence included visual and lateral prefrontal regions, positive valence activated middle temporal and orbitofrontal areas. Importantly, distinct arousal-by-valence interactions were present in anterior insula (negative pictures), and in occipital cortex, parahippocampal gyrus and posterior cingulate (positive pictures). These data demonstrate that the brain not only differentiates between valence and arousal but also responds to specific combinations of these two, thereby highlighting the sophisticated nature of emotion processing in (female) human subjects.
Brain & Cognition, in press
Valence and arousal are thought to be the primary dimensions of human emotion. However, the degree to which valence and arousal interact in determining brain responses to emotional pictures is still elusive. This functional MRI study aimed to delineate neural systems responding to valence and arousal, and their interaction. We measured neural activation in healthy females (N=23) to affective pictures using a 2 (Valence)x2 (Arousal) design. Results show that arousal was preferentially processed by middle temporal gyrus, hippocampus and ventrolateral prefrontal cortex. Regions responding to negative valence included visual and lateral prefrontal regions, positive valence activated middle temporal and orbitofrontal areas. Importantly, distinct arousal-by-valence interactions were present in anterior insula (negative pictures), and in occipital cortex, parahippocampal gyrus and posterior cingulate (positive pictures). These data demonstrate that the brain not only differentiates between valence and arousal but also responds to specific combinations of these two, thereby highlighting the sophisticated nature of emotion processing in (female) human subjects.
ARTICLE UPDATE - An electrophysiological investigation into the automaticity of emotional face processing in high versus low trait anxious individuals
Holmes A, Nielsen MK, Tipper S, Green S.
Cognitive, Affective, Behavioral Neuroscience, 9, 323-334
To examine the extent of automaticity of emotional face processing in high versus low trait anxious participants, event-related potentials (ERPs) were recorded to emotional (fearful, happy) and neutral faces under varying task demands (low load, high load). Results showed that perceptual encoding of emotional faces, as reflected in P1 and early posterior negativity components, was unaffected by the availability of processing resources. In contrast, the postperceptual registration and storage of emotion-related information, as reflected in the late positive potential component at frontal locations, was influenced by the availability of processing resources, and this effect was further modulated by level of trait anxiety. Specifically, frontal ERP augmentations to emotional faces were eliminated in the more demanding task for low trait anxious participants, whereas ERP enhancements to emotional faces were unaffected by task load in high trait anxious participants. This result suggests greater automaticity in processing affective information in high trait anxious participants.
Cognitive, Affective, Behavioral Neuroscience, 9, 323-334
To examine the extent of automaticity of emotional face processing in high versus low trait anxious participants, event-related potentials (ERPs) were recorded to emotional (fearful, happy) and neutral faces under varying task demands (low load, high load). Results showed that perceptual encoding of emotional faces, as reflected in P1 and early posterior negativity components, was unaffected by the availability of processing resources. In contrast, the postperceptual registration and storage of emotion-related information, as reflected in the late positive potential component at frontal locations, was influenced by the availability of processing resources, and this effect was further modulated by level of trait anxiety. Specifically, frontal ERP augmentations to emotional faces were eliminated in the more demanding task for low trait anxious participants, whereas ERP enhancements to emotional faces were unaffected by task load in high trait anxious participants. This result suggests greater automaticity in processing affective information in high trait anxious participants.
ARTICLE UPDATE - Taboo words: The effect of emotion on memory for peripheral information.
Guillet R, Arndt J.
Memory & Cognition, 37, 866-879
In three experiments, we examined memory for peripheral information that occurred in the same context as emotion-inducing information. In the first two experiments, participants studied either a sentence (Experiment 1) or a pair of words (Experiments 2A-2C) containing a neutral peripheral word, as well as a neutral, negative-valence, or taboo word, to induce an emotional response. At retrieval, the participants were asked to recall the neutral peripheral word from a sentence fragment or emotion-inducing word cue. In Experiment 3, we presented word pairs at encoding and tested memory with associative recognition. In all three experiments, memory for peripheral words was enhanced when it was encoded in the presence of emotionally arousing taboo words but not when it was encoded in the presence of words that were only negative in valence. These data are consistent with priority-binding theory (MacKay et al., 2004) and inconsistent with the attention-narrowing hypothesis (Easterbrook, 1959), as well as with object-based binding theory (Mather, 2007).
Memory & Cognition, 37, 866-879
In three experiments, we examined memory for peripheral information that occurred in the same context as emotion-inducing information. In the first two experiments, participants studied either a sentence (Experiment 1) or a pair of words (Experiments 2A-2C) containing a neutral peripheral word, as well as a neutral, negative-valence, or taboo word, to induce an emotional response. At retrieval, the participants were asked to recall the neutral peripheral word from a sentence fragment or emotion-inducing word cue. In Experiment 3, we presented word pairs at encoding and tested memory with associative recognition. In all three experiments, memory for peripheral words was enhanced when it was encoded in the presence of emotionally arousing taboo words but not when it was encoded in the presence of words that were only negative in valence. These data are consistent with priority-binding theory (MacKay et al., 2004) and inconsistent with the attention-narrowing hypothesis (Easterbrook, 1959), as well as with object-based binding theory (Mather, 2007).
Monday, August 10, 2009
ARTICLE UPDATE - Tuning the brain for novelty detection under emotional threat: the role of increasing gamma phase-synchronization.
Garcia-Garcia M, Yordanova J, Kolev V, Domínguez-Borràs J, Escera C.
Neuroimage, in press
Effective orienting of attention towards novel events is crucial for survival, particularly if they occur in a dangerous situation. This is why stimuli with emotional value are more efficient in capturing attention than neutral stimuli, and why the processing of unexpected novel stimuli is enhanced under a negative emotional context. Here we measured the phase-synchronization (PS) of gamma-band responses (GBR) from human EEG scalp-recordings during performance of a visual discrimination task in which task-irrelevant standard and novel sounds were presented in either a neutral or a negative emotional context, in order to elucidate the brain mechanisms by which emotion tunes the processing of novel events. Visual task performance was distracted by novel sounds, and this distraction was enhanced by the negative emotional context. Similarly, gamma PS was enhanced after novel as compared to standard sounds and it was also larger to auditory stimuli in the negative than in the neutral emotional context, reflecting the synchronization of neural networks for increasing of attentional processing. Remarkably, the larger PS increase of GBR after novel sounds in the negative as compared to the neutral emotional context over midline and right frontal regions reveals that a negative emotional context tunes novelty processing by means of the PS of brain activity in the gamma frequency band around 40 Hz in specific neural networks.
Neuroimage, in press
Effective orienting of attention towards novel events is crucial for survival, particularly if they occur in a dangerous situation. This is why stimuli with emotional value are more efficient in capturing attention than neutral stimuli, and why the processing of unexpected novel stimuli is enhanced under a negative emotional context. Here we measured the phase-synchronization (PS) of gamma-band responses (GBR) from human EEG scalp-recordings during performance of a visual discrimination task in which task-irrelevant standard and novel sounds were presented in either a neutral or a negative emotional context, in order to elucidate the brain mechanisms by which emotion tunes the processing of novel events. Visual task performance was distracted by novel sounds, and this distraction was enhanced by the negative emotional context. Similarly, gamma PS was enhanced after novel as compared to standard sounds and it was also larger to auditory stimuli in the negative than in the neutral emotional context, reflecting the synchronization of neural networks for increasing of attentional processing. Remarkably, the larger PS increase of GBR after novel sounds in the negative as compared to the neutral emotional context over midline and right frontal regions reveals that a negative emotional context tunes novelty processing by means of the PS of brain activity in the gamma frequency band around 40 Hz in specific neural networks.
ARTICLE UPDATE - Tell me about it: Neural activity elicited by emotional pictures and preceding descriptions.
Macnamara A, Foti D, Hajcak G.
Emotion, 9, 531-543
Emotional pictures elicit enhanced parietal positivities beginning around 300 ms following stimulus presentation. The magnitude of these responses, however, depends on both intrinsic (stimulus-driven) and extrinsic (context-driven) factors. In the present study, event-related potentials were recorded while participants viewed unpleasant and neutral pictures that were described either more neutrally or more negatively prior to presentation; temporospatial principal components analysis identified early and late positivities: Both emotional images and descriptions had independent and additive effects on early (334 ms) and midlatency (1,066 ms) positivities, whereas the latest positivity (1,688 ms) was sensitive only to description type. Results are discussed with regard to the time course of automatic and controlled processing of emotional stimuli.
Emotion, 9, 531-543
Emotional pictures elicit enhanced parietal positivities beginning around 300 ms following stimulus presentation. The magnitude of these responses, however, depends on both intrinsic (stimulus-driven) and extrinsic (context-driven) factors. In the present study, event-related potentials were recorded while participants viewed unpleasant and neutral pictures that were described either more neutrally or more negatively prior to presentation; temporospatial principal components analysis identified early and late positivities: Both emotional images and descriptions had independent and additive effects on early (334 ms) and midlatency (1,066 ms) positivities, whereas the latest positivity (1,688 ms) was sensitive only to description type. Results are discussed with regard to the time course of automatic and controlled processing of emotional stimuli.
ARTICLE UPDATE - Immediacy bias in emotion perception: Current emotions seem more intense than previous emotions.
Van Boven L, White K, Huber M.
Journal of Experimental Psychology: General, 138, 368-382
People tend to perceive immediate emotions as more intense than previous emotions. This immediacy bias in emotion perception occurred for exposure to emotional but not neutral stimuli (Study 1), when emotional stimuli were separated by both shorter (2 s; Studies 1 and 2) and longer (20 min; Studies 3, 4, and 5) delays, and for emotional reactions to pictures (Studies 1 and 2), films (Studies 3 and 4), and descriptions of terrorist threats (Study 5). The immediacy bias may be partly caused by immediate emotion's salience, and by the greater availability of information about immediate compared with previous emotion. Consistent with emotional salience, when people experienced new emotions, they perceived previous emotions as less intense than they did initially (Studies 3 and 5)-a change in perception that did not occur when people did not experience a new immediate emotion (Study 2). Consistent with emotional availability, reminding people that information about emotions naturally decays from memory reduced the immediacy bias by making previous emotions seem more intense (Study 4). Discussed are implications for psychological theory and other judgments and behaviors.
Journal of Experimental Psychology: General, 138, 368-382
People tend to perceive immediate emotions as more intense than previous emotions. This immediacy bias in emotion perception occurred for exposure to emotional but not neutral stimuli (Study 1), when emotional stimuli were separated by both shorter (2 s; Studies 1 and 2) and longer (20 min; Studies 3, 4, and 5) delays, and for emotional reactions to pictures (Studies 1 and 2), films (Studies 3 and 4), and descriptions of terrorist threats (Study 5). The immediacy bias may be partly caused by immediate emotion's salience, and by the greater availability of information about immediate compared with previous emotion. Consistent with emotional salience, when people experienced new emotions, they perceived previous emotions as less intense than they did initially (Studies 3 and 5)-a change in perception that did not occur when people did not experience a new immediate emotion (Study 2). Consistent with emotional availability, reminding people that information about emotions naturally decays from memory reduced the immediacy bias by making previous emotions seem more intense (Study 4). Discussed are implications for psychological theory and other judgments and behaviors.
ARTICLE UPDATE - What factors need to be considered to understand emotional memories?
Kensinger EA.
Emotional Review, 1, 120-121
In my original review (this issue), I proposed that to understand the effects of emotion on memory accuracy, we must look beyond effects of arousal and consider the contribution of valence. In discussing this proposal, the commentators raise a number of excellent points that hone in on the question of when valence does (and does not) account for emotion's effects on memory accuracy. Though future research will be required to resolve this issue more fully, in this brief response, I address some of the concerns outlined by the commentators and suggest a few steps that may help to elucidate the dimensions that should be incorporated in models of emotional memory.
Emotional Review, 1, 120-121
In my original review (this issue), I proposed that to understand the effects of emotion on memory accuracy, we must look beyond effects of arousal and consider the contribution of valence. In discussing this proposal, the commentators raise a number of excellent points that hone in on the question of when valence does (and does not) account for emotion's effects on memory accuracy. Though future research will be required to resolve this issue more fully, in this brief response, I address some of the concerns outlined by the commentators and suggest a few steps that may help to elucidate the dimensions that should be incorporated in models of emotional memory.
ARTICLE UPDATE - Why people rehearse their memories: Frequency of use and relations to the intensity of emotions associated with autobiographical memo
Walker WR, Skowronski JJ, Gibbons JA, Vogl RJ, Ritchie TD.
Memory, in press
People may choose to rehearse their autobiographical memories in silence or to disclose their memories with other people. This paper focuses on five types of memory rehearsal: involuntary rehearsal, rehearsal to maintain an event memory, rehearsal to re-experience the emotion of an event, rehearsal to understand an event, or rehearsal for social communication. A total of 337 participants recalled event memories, provided estimates of how often each event was rehearsed and for what reason, and rated the affective characteristics of the events. Rehearsal frequency was highest for social communication and lowest for rehearsals aimed at understanding events. For many rehearsal types, rehearsal was more frequent for positive than negative events. Frequently rehearsed events tended to show less affective fading. The pattern changed when events were socially rehearsed. For positive events, increased social rehearsal was related to a reduction in affective fading. For negative events, increased social rehearsal was associated with increased affective fading.
Memory, in press
People may choose to rehearse their autobiographical memories in silence or to disclose their memories with other people. This paper focuses on five types of memory rehearsal: involuntary rehearsal, rehearsal to maintain an event memory, rehearsal to re-experience the emotion of an event, rehearsal to understand an event, or rehearsal for social communication. A total of 337 participants recalled event memories, provided estimates of how often each event was rehearsed and for what reason, and rated the affective characteristics of the events. Rehearsal frequency was highest for social communication and lowest for rehearsals aimed at understanding events. For many rehearsal types, rehearsal was more frequent for positive than negative events. Frequently rehearsed events tended to show less affective fading. The pattern changed when events were socially rehearsed. For positive events, increased social rehearsal was related to a reduction in affective fading. For negative events, increased social rehearsal was associated with increased affective fading.
Monday, August 03, 2009
ARTICLE UPDATE - Normative data on development of neural and behavioral mechanisms underlying attention orienting toward social-emotional stimuli: An
Lindstrom K, Guyer AE, Mogg K, Bradley BP, Fox NA, Ernst M, Nelson EE, Leibenluft E, Britton JC, Monk CS, Pine DS, Bar-Haim Y.
Brain Research, in press
The ability of positive and negative facial signals to influence attention orienting is crucial to social functioning. Given the dramatic developmental change in neural architecture supporting social function, positive and negative facial cues may influence attention orienting differently in relatively young or old individuals. However, virtually no research examines such age-related differences in the neural circuitry supporting attention orienting to emotional faces. We examined age-related correlations in attention-orienting biases to positive and negative face emotions in a healthy sample (N=37; 9-40 years old) using functional magnetic resonance imaging and a dot-probe task. The dot-probe task in an fMRI setting yields both behavioral and neural indices of attention biases towards or away from an emotional cue (happy or angry face). In the full sample, angry-face attention bias scores did not correlate with age, and age did not correlate with brain activation to angry faces. However, age did positively correlate with attention bias towards happy faces; age also negatively correlated with left cuneus and left caudate activation to a happy-bias fMRI contrast. Secondary analyses suggested age-related changes in attention bias to happy faces. The tendency in younger children to direct attention away from happy faces (relative to neutral faces) was diminished in the older age groups, in tandem with increasing neural deactivation. Implications for future work on developmental changes in attention-emotion processing are discussed.
Brain Research, in press
The ability of positive and negative facial signals to influence attention orienting is crucial to social functioning. Given the dramatic developmental change in neural architecture supporting social function, positive and negative facial cues may influence attention orienting differently in relatively young or old individuals. However, virtually no research examines such age-related differences in the neural circuitry supporting attention orienting to emotional faces. We examined age-related correlations in attention-orienting biases to positive and negative face emotions in a healthy sample (N=37; 9-40 years old) using functional magnetic resonance imaging and a dot-probe task. The dot-probe task in an fMRI setting yields both behavioral and neural indices of attention biases towards or away from an emotional cue (happy or angry face). In the full sample, angry-face attention bias scores did not correlate with age, and age did not correlate with brain activation to angry faces. However, age did positively correlate with attention bias towards happy faces; age also negatively correlated with left cuneus and left caudate activation to a happy-bias fMRI contrast. Secondary analyses suggested age-related changes in attention bias to happy faces. The tendency in younger children to direct attention away from happy faces (relative to neutral faces) was diminished in the older age groups, in tandem with increasing neural deactivation. Implications for future work on developmental changes in attention-emotion processing are discussed.
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