ARTICLE UPDATE - The beneficial effects of additional task load, positive affect, and instruction on the attentional blink.

Olivers CN, Nieuwenhuis S.

Journal of Experimental Psychology: Human Perception & Performances, 32, 364-379

The attentional blink reflects the impaired ability to identify the 2nd of 2 targets presented in close succession--a phenomenon that is generally thought to reflect a fundamental cognitive limitation. However, the fundamental nature of this impairment has recently been called into question by the counterintuitive finding that task-irrelevant mental activity improves attentional blink performance (C. N. L. Olivers & S. Nieuwenhuis, 2005). The present study found a reduced attentional blink when participants concurrently performed an additional memory task, viewed pictures of positive affective content, or were instructed to focus less on the task. These findings support the hypothesis that the attentional blink is due to an overinvestment of attentional resources in stimulus processing, a suboptimal processing mode that can be counteracted by manipulations promoting divided attention.

*Note that their results published in 2005 has been questioned

ARTICLE UPDATE - The impact of emotion on perception: bias or enhanced processing?

Zeelenberg R, Wagenmakers EJ, Rotteveel M.

Psychological Science, 17, 287-291

Recent studies have shown that emotionally significant stimuli are often better identified than neutral stimuli. It is not clear, however, whether these results are due to enhanced perceptual processing or to a bias favoring the identification of emotionally significant stimuli over neutral stimuli. The present study used a two-alternative forced-choice perceptual identification task to disentangle the effects of bias and enhanced processing. We found that emotionally significant targets were better identified than neutral targets. In contrast, the emotional significance of the foil alternative had no effect on performance. The present results support the hypothesis that perceptual encoding of emotionally significant stimuli is enhanced.

ARTICLE UPDATE - Emotion facilitates perception and potentiates the perceptual benefits of attention.

Phelps EA, Ling S, Carrasco M.

Psychological Science, 17, 292-299.

Does emotion affect how people see? We investigated the effects of emotion and attention, as well as their conjoint effect, on contrast sensitivity, a dimension of early vision. We manipulated the emotional valence and the attentional distribution of cues preceding a target stimulus and asked observers to judge the orientation of the target as contrast varied. This study provides the first behavioral evidence that (a) emotion enhances contrast sensitivity irrespective of attention and (b) emotion potentiates the effect of attention on contrast sensitivity.

ARTICLE UPDATE - Emotional category data on images from the International Affective Picture System.

Mikels JA, Fredrickson BL, Larkin GR, Lindberg CM, Maglio SJ, Reuter-Lorenz PA.

Behavioural Research Methods, 37, 626-630

The International Affective Picture System (IAPS) is widely used in studies of emotion and has been characterized primarily along the dimensions of valence, arousal, and dominance. Even though research has shown that the IAPS is useful in the study of discrete emotions, the categorical structure of the IAPS has not been characterized thoroughly. The purpose of the present project was to collect descriptive emotional category data on subsets of the LAPS in an effort to identify images that elicit onediscrete emotion more than others. These data reveal multiple emotional categories for the images and indicate that this image set has great potential in the investigation of discrete emotions. This article makes these data available to researchers with such interests. Data for all the pictures are archived at www.psychonomic.org/archive/. (not available on line yet)

ARTICLE UPDATE - Attention does not modulate neural responses to social stimuli in autism spectrum disorders

Geoffrey Bird, Caroline Catmur, Giorgia Silani, Chris Frith and Uta Frith

NeuroImage, in press

We investigated whether individuals with autism spectrum disorders (ASD) would show attentional modulation for social (face) and non-social (house) stimuli. Sixteen individuals with ASD and 16 matched control participants completed a task in which pairs of face and house stimuli were present on every trial, with one of the pairs randomly assigned to attended locations and the other to unattended locations. Both mass-univariate (SPM) and region of interest analyses suggested that responses to houses were modulated by attention in both groups, but that only the control participants demonstrated attentional modulation of face-selective regions. Thus, the participants with ASD demonstrated a lack of attentional modulation which was particularly evident for the social stimulus. Analyses of effective connectivity indicated that these results were due to a failure of attention to modulate connectivity between extrastriate areas and V1. We discuss how these results may suggest a mechanism to explain the reduced salience of social stimuli in ASD.

ARTICLE UPDATE - Non-conscious recognition of emotional body language.

de Gelder B, Hadjikhani N.

Neuroreport, 17, 583-586

Patients with cortical blindness can reliably perceive some facial expressions even if they are unaware of their percept. We examined whether emotional body language may also be recognized in the absence of the primary visual cortex and without conscious stimulus perception. We presented emotional and neutral body images in the blind field of a patient with unilateral striate cortex damage. Using functional magnetic resonance imaging, we measured activation following presentation to the blind hemifield of whole body images (happy, neutral) with the face blurred. Unseen happy body images selectively activated area MT and the pulvinar nucleus of the thalamus, while unseen instrumental neutral body images activated the premotor cortex. Our results show that in the absence of the striate cortex implicit bodily emotion perception may be possible.

ARTICLE UPDATE - Emotional information processing in mood disorders: a review of behavioral and neuroimaging findings.

Leppanen JM.

Current Opinions in Psychiatry, 19, 34-39.

A relatively long history of research has shown that mood disorders are associated with abnormalities in the processing of emotional stimuli. Only the most recent studies, however, have begun to elucidate the specificity and neural basis of these abnormalities. This article reviews and discusses the results of these studies. RECENT FINDINGS: Individuals diagnosed with major depressive disorder exhibit an attentional bias toward negative emotional cues (e.g. sad faces), an attentional bias away from positive emotional cues (e.g. happy faces), and an enhanced memory for negative emotional material. Compared with healthy controls, individuals with major depressive disorder show increased neural activity in response to sad faces and diminished neural activity in response to happy faces in emotion-related brain circuits (e.g. amygdala and ventral striatum). Some of these abnormalities in the processing of emotional information persist after symptom remission and they have also been found in healthy individuals who are at heightened risk for the development of mood disorders. SUMMARY: The reviewed data show that major depressive disorder involves specific abnormalities in the cognitive and neural processing of emotional information and that these abnormalities may potentially contribute to the vulnerability for negative emotion and onset of depressive episodes.

ARTICLE UPDATE - They know the words, but not the music: Affective and semantic priming in individuals with psychopathy.

Blair KS, Richell RA, Mitchell DG, Leonard A, Morton J, Blair RJ.

Biological Psychology, in press

Previous work has indicated dysfunctional affect-language interactions in individuals with psychopathy through use of the lexical decision task. However, it has been uncertain as to whether these deficits actually reflect impaired affect-language interactions or a more fundamental deficit in general semantic processing. In this study, we examined affective priming and semantic priming (dependent measures were reaction times and error rates) in individuals with psychopathy and comparison individuals, classified according to the psychopathy checklist revised (PCL-R) [Hare, R.D., 1991. The Hare Psychopathy Checklist-Revised. Multi-Health Systems, Toronto, Ont.]. Individuals with psychopathy showed significantly less affective priming relative to comparison individuals. In contrast, the two groups showed comparable levels of semantic priming. The results are discussed with reference to current models of psychopathy.

ARTICLE UPDATE- Increased positive emotional memory after repetitive transcranial magnetic stimulation over the orbitofrontal cortex

Schutter DJ, van Honk J.

Journal of Psychiatry Neuroscience, 31, 101-104.

Several studies have demonstrated increased left orbitofrontal cortex (OFC) activity during negative and depressed mood. These mood states have also been associated with reduced memory for positive emotional stimuli. The aim of the present study was to investigate whether slow, inhibitory repetitive transcranial magnetic stimulation (rTMS) over the left OFC would improve memory for positive material. METHODS: We carried out a study with a double-blind, within-subjects design, in which 12 healthy volunteers received 20 minutes of slow rTMS over the left OFC, placebo treatment over the left OFC and rTMS over the left dorsolateral portion of the prefrontal cortex. Effects on memory for fearful and happy faces were investigated. RESULTS: Memory for happy faces was significantly improved after rTMS over the left OFC compared with placebo (t(10) = 2.4, p = 0.037). CONCLUSIONS: These findings suggest a role of the OFC in positive emotional memory, which is in accordance with neuroimaging and neuropsychological data. It may be argued that dense projections from the OFC to the limbic emotional circuit are involved in emotional memory and, therefore, play a role in the effects of rTMS that we observed.

ARTICLE UPDATE - Compensatory strategies in processing facial emotions: Evidence from prosopagnosia.

Baudouin JY, Humphreys GW.

Neuropsychologica, in press

We report data on the processing of facial emotion in a prosopagnosic patient (H.J.A.). H.J.A. was relatively accurate at discriminating happy from angry upright faces, but he performed at chance when the faces were inverted. Furthermore, with upright faces there was no configural interference effect on emotion judgements, when face parts expressing different emotions were aligned to express a new emergent emotion. We propose that H.J.A.'s emotion judgements relied on local rather than on configural information, and this local information was disrupted by inversion. A compensatory strategy, based on processing local face parts, can be sufficient to process at least some facial emotions.

ARTICLE UPDATE - Stimulus novelty and emotion perception: the near absence of habituation in the visual cortex

Schupp HT, Stockburger J, Codispoti M, Junghofer M, Weike AI, Hamm AO.

Neuroreport, 17, 365-369

In rapid serial visual presentation of pictures, an early event-related brain potential component shows enlarged negativity over occipital regions for emotional pictures compared with neutral pictures. The present study examined whether the processing of emotional target pictures varies as a function of stimulus repetition. Accordingly, pictures of erotica, neutral contents, and mutilations were repeatedly presented (90 times) while the electroencephalogram was recorded with a 129 dense sensor array. As in previous studies, emotional pictures were associated with a larger posterior negativity than neutral pictures. Furthermore, differential emotion processing did not vary as a function of stimulus repetition and was similarly expressed across blocks of picture presentation. These findings suggest the near absence of habituation in differential emotion processing during perceptual processing.

ARTICLE UPDATE - Between-subject transfer of emotional information evokes specific pattern of amygdala activation.

Knapska E, Nikolaev E, Boguszewski P, Walasek G, Blaszczyk J, Kaczmarek L, Werka T.

PNAS, 103, 3859-3864

Emotional states displayed by an animal or a human can seriously affect behavior of their conspecifics. The amygdala plays a crucial role in the processing of emotions. In this study, we describe an experimental rat model of between-subject transfer of emotional information and its effects on activation of the amygdala. The rats were kept in pairs, and one animal (designated as "demonstrator") was treated to specific behavioral training of either foot-shock-reinforced context conditioning or just exposure to a novel context. We next examined the influence of the demonstrators on the exploratory behavior of their cagemates (called "observers") and the observers' performance of the acoustic startle response. We report that we can distinguish both groups of observers from the control animals (as shown by startle-response measure) and distinguish between observers (by means of indexing the exploration), with respect to whether they were paired with demonstrators treated to different experimental conditions. Furthermore, we show that the observers have most of their amygdala activated (as revealed by c-Fos mapping) to the same level as the demonstrators and, in the case of the central amygdala, to an even higher level. Moreover, the level of c-Fos expression in the observers reflected the specific behavioral treatment of the demonstrators with whom they were paired. Thus, in this study, we have shown that undefined emotional information transferred by a cohabitant rat can be evaluated and measured and that it evokes very strong and information-specific activation of the amygdala.

ARTICLE UPDATE - Anxiety and sensitivity to eye gaze in emotional faces.

Holmes A, Richards A, Green S.

Brain & Cognition, 60, 282-294

This paper reports three studies in which stronger orienting to perceived eye gaze direction was revealed when observers viewed faces showing fearful or angry, compared with happy or neutral, emotional expressions. Gaze-related spatial cueing effects to laterally presented fearful faces and centrally presented angry faces were also modulated by the anxiety level of participants, with high- but not low-state anxious individuals revealing enhanced shifts of attention. In contrast, both high- and low-state anxious individuals demonstrated enhanced orienting to averted gaze when viewing laterally presented angry faces. These results provide novel evidence for the rapid integration of facial expression and gaze direction information, and for the regulation of gaze-cued attention by both the emotion conveyed in the perceived face and the degree of anxiety experienced by the observer.

ARTICLE UPDATE - Amygdala Activity Is Associated with the Successful Encoding of Item, But Not Source, Information for Positive and Negative Stimuli

Elizabeth A. Kensinger and Daniel L. Schacter

The Journal of Neuroscience, 26, 2564-2570

It has been debated whether the link between amygdala activity and subsequent memory is equally strong for positive and negative information. Moreover, it has been unclear whether amygdala activity at encoding corresponds with enhanced memory for all contextual aspects of the presentation of an emotional item, or whether amygdala activity primarily enhances memory for the emotional item itself. In the present functional magnetic resonance imaging study, participants encoded positive and negative stimuli while performing one of two tasks (judgment of animacy or commonness). Amygdala activity at encoding was related to subsequent memory for the positive and negative items but not to subsequent memory for the task performed. Amygdala activity showed no relationship to subsequent-memory performance for the neutral items. Regardless of the emotional content of the items, activity in the entorhinal cortex corresponded with subsequent memory for the item but not with memory for the task performed, whereas hippocampal activity corresponded with subsequent memory for the task performed. These results are the first to demonstrate that the amygdala can be equally engaged during the successful encoding of positive and negative items but that its activity does not facilitate the encoding of all contextual elements present during an encoding episode. The results further suggest that dissociations within the medial temporal lobe sometimes noted for nonemotional information (i.e., activity in the hippocampus proper leading to later memory for context, and activity in the entorhinal cortex leading to later memory for an item but not its context) also hold for emotional information.

ARTICLE UPDATE - Towards the neurobiology of emotional body language

de Gelder B.

Nature Review Neuroscience, 7, 242-249

People's faces show fear in many different circumstances. However, when people are terrified, as well as showing emotion, they run for cover. When we see a bodily expression of emotion, we immediately know what specific action is associated with a particular emotion, leaving little need for interpretation of the signal, as is the case for facial expressions. Research on emotional body language is rapidly emerging as a new field in cognitive and affective neuroscience. This article reviews how whole-body signals are automatically perceived and understood, and their role in emotional communication and decision-making.

ARTICLE UPDATE - Attentional modulation of the amygdala varies with personality

Steven B. Most, Marvin M. Chun, Matthew R. Johnson and Kent A. Kiehl

NeuroImage, in press

The amygdala is implicated in emotional processing, and its rich subcortical connections have led to suggestions that processing of emotional stimuli occurs independently of attention. Using a novel attentional manipulation in conjunction with fMRI, we showed that emotion-related amygdala activity was modulated by attention, but that the degree of such modulation correlated with the personality variable harm avoidance, associated with trait anxiety. Participants ignored emotional distractors while searching through a rapid stream of pictures for a target, about which they were provided either specific or nonspecific descriptive information (e.g., “look for a building” versus “look for a landscape or building”). Thus, they employed either a specific or a nonspecific attentional set in order to find the target and ignore distractors. In response to irrelevant emotional distractors, low harm-avoidant participants had relatively little emotion-related amygdala activity regardless of whether they maintained a specific or nonspecific attentional set. High harm-avoidant participants, however, showed strong emotion-related amygdala activity when maintaining a nonspecific attentional set and lower amygdala activity when maintaining a specific attentional set. This decrease was accompanied by increased activation of the rostral anterior cingulate cortex (ACC), which is often linked with the resolution of affective interference. In addition to demonstrating individual differences in attentional modulation of the amygdala, these results may indicate that the rostral ACC is sensitive to the increased effort that high harm-avoidant individuals must recruit in order to modulate amygdala responsivity.

ARTICLE UPDATE - Facial expressions and complex IAPS pictures: Common and differential networks

Jennifer C. Britton, Stephan F. Taylor, Keith D. Sudheimer and Israel Liberzon

NeuroImage, in press

Neuroimaging studies investigating emotion have commonly used two different visual stimulus formats, facial expressions of emotion or emotionally evocative scenes. However, it remains an important unanswered question whether or not these different stimulus formats entail the same processes. Facial expressions of emotion may elicit more emotion recognition/perception, and evocative pictures may elicit more direct experience of emotion. In spite of these differences, common areas of activation have been reported across different studies, but little work has investigated activations in response to the two stimulus formats in the same subjects. In this fMRI study, we compared BOLD activation patterns to facial expression of emotions and to complex emotional pictures from the International Affective Picture System (IAPS) to determine if these stimuli would activate similar or distinct brain regions. Healthy volunteers passively viewed blocks of expressive faces and IAPS pictures balanced for specific emotion (happy, sad, anger, fear, neutral), interleaved with blocks of fixation. Eye movement, reaction times, and off-line subjective ratings including discrete emotion, valence, and arousal were also recorded. Both faces and IAPS pictures activated similar structures, including the amygdala, posterior hippocampus, ventromedial prefrontal cortex, and visual cortex. In addition, expressive faces uniquely activated the superior temporal gyrus, insula, and anterior cingulate more than IAPS pictures, despite the faces being less arousing. For the most part, these regions were activated in response to all specific emotions; however, some regions responded only to a subset.

ARTICLE UPDATE - Neural systems for orienting attention to the location of threat signals: An event-related fMRI study

Gilles Pourtois, Sophie Schwartz, Mohamed L. Seghier, François Lazeyras and Patrik Vuilleumier

NeuroImage, in press

Attention may reflexively shift towards the location of perceived threats, but it is still unclear how these spatial biases recruit the distributed fronto-parietal cortical networks involved in other aspects of selective attention. We used event-related fMRI to determine how brain responses to a neutral visual target are influenced by the emotional expression of faces appearing at the same location during a covert orienting task. On each trial, two faces were briefly presented, one in each upper visual field (one neutral and one emotional, fearful or happy), followed by a unilateral target (a small horizontal or vertical bar) replacing one of the faces. Participants had to discriminate the target orientation, shown on the same (valid) or opposite (invalid) side as the emotional face. Trials with faces but no subsequent target (cue-only trials) were included to disentangle activation due to emotional cues from their effects on target detection. We found increased responses in bilateral temporo-parietal areas and right occipito-parietal cortex for fearful faces relative to happy faces, unrelated to the subsequent target and cueing validity. More critically, we found a selective modulation of intraparietal and orbitofrontal cortex for targets following an invalid fearful face, as well as an increased visual response in right lateral occipital cortex for targets following a valid fearful face. No such effects were observed with happy faces. These results demonstrate that fearful faces can act as exogenous cues by increasing sensory processing in extrastriate cortex for a subsequent target presented at the same location, but also produce a cost in disengaging towards another location by altering the response of IPS to invalidly cued targets. Neural mechanisms responsible for orienting attention towards emotional vs. non-emotional stimuli are thus partly shared in parietal and visual areas, but also partly distinct.

ARTICLE UPDATE - Task and content modulate amygdala-hippocampal connectivity in emotional retrieval.

Smith AP, Stephan KE, Rugg MD, Dolan RJ.

Neuron, 16, 631-638.

The ability to remember emotional events is crucial for adapting to biologically and socially significant situations. Little is known, however, about the nature of the neural interactions supporting the integration of mnemonic and emotional information. Using fMRI and dynamic models of effective connectivity, we examined regional neural activity and specific interactions between brain regions during a contextual memory retrieval task. We independently manipulated emotional context and relevance of retrieved emotional information to task demands. We show that retrieval of emotionally valenced contextual information is associated with enhanced connectivity from hippocampus to amygdala, structures crucially involved with encoding of emotional events. When retrieval of emotional information is relevant to current behavior, amygdala-hippocampal connectivity increases bidirectionally, under modulatory influences from orbitofrontal cortex, a region implicated in representation of affective value and behavioral guidance. Our findings demonstrate that both memory content and behavioral context impact upon large scale neuronal dynamics underlying emotional retrieval.

ARTICLE UPDATE - Does emotion help or hinder immediate memory? Arousal versus priority-binding mechanisms.

Hadley CB, Mackay DG.

Journal of Experimental Psychology: Learning, Memory and Cognition, 32, 79-88.

People recall taboo words better than neutral words in many experimental contexts. The present rapid serial visual presentation (RSVP) experiments demonstrated this taboo-superiority effect for immediate recall of mixed lists containing taboo and neutral words matched for familiarity, length, and category coherence. Under binding theory (MacKay et al., 2004), taboo superiority reflects an interference effect: Because the emotional reaction system prioritizes binding mechanisms for linking the source of an emotion to its context, taboo words capture the mechanisms for encoding list context in mixed lists, impairing the encoding of adjacent neutral words when RSVP rates are sufficiently rapid. However, for pure or unmixed lists, binding theory predicted no better recall of taboo-only than of neutral-only lists at fast or slow rates. Present results supported this prediction, suggesting that taboo superiority in immediate recall reflects context-specific binding processes, rather than context-free arousal effects, or emotion-linked differences in rehearsal, processing time, output interference, time-based decay, or guessing biases.