Biomedical subjects

Beatrice de Gelder

Publications and source records attributed to Beatrice de Gelder.

At least 19 recordsLinked to original sources

PubMed2006

Fast recognition of social emotions takes the whole brain: interhemispheric cooperation in the absence of cerebral asymmetry.

Hemispheric asymmetry in emotional perception has been traditionally studied for basic emotions and very little is known about laterality for more complex social emotions. Here, we used the "redundant target paradigm" to investigate interhemispheric asymmetry and cooperation for two social emotions in healthy subjects. Facial expressions of flirtatiousness or arrogance were briefly presented either unilaterally in the left (LVF) or right visual field (RVF), or simultaneously to both visual fields (BVF) while participants responded to the target expression (flirtatious or arrogant, counterbalanced between blocks). In bilateral conditions the faces could show the same emotion (congruent condition) or two different expressions (incongruent condition). No difference between unilateral presentations was found, suggesting that the perception of social emotions is not hemispherically lateralized. Responses were faster and more accurate in bilateral displays with two emotionally congruent but physically different faces (i.e., a male and a female expressing the same emotion) than in unilateral conditions. This "redundant target effect" was consistent with a neural summation model, thereby showing that interhemispheric cooperation may occur for social emotions despite major perceptual differences between faces posing the same expression.

Adult↗

PubMed2006

Autonomic reactivity to sensory stimulation is related to consciousness level after severe traumatic brain injury.

OBJECTIVE: To examine changes in the activity of the autonomic nervous system (ANS) that are related to recovery to consciousness in the post-acute phase after severe traumatic brain injury (sTBI). METHODS: Skin conductance and heart rate reactivity to sensory stimulation were recorded every 2 weeks for an average period of 3.5 months in 16 adolescent patients, during the assessment of their level of consciousness (LoC), and their cognitive and functional behaviour. RESULTS: Both heart rate variability (HRV) and skin conductance level (SCL) in reaction to sensory stimulation changed with recovery to consciousness. Indices of HRV and SCL that represent sympathetic activity of the autonomic nervous system (ANS) increased with recovery, whereas indices that represent parasympathetic activity decreased. In addition, we observed an increase in sympathovagal balance of the ANS with recovery. CONCLUSIONS: Recovery to consciousness determined by clinical observation in sTBI in the post-acute phase is related to changes in SCL and HRV during sensory stimulation. ANS reactivity to environmental stimulation can therefore give objective supplementary information about the clinical state of sTBI patients, and can contribute to decision-making in the treatment policy of unresponsive patients. SIGNIFICANCE: These findings demonstrate that autonomic reactivity can be informative concerning how a severely damaged nervous system reacts to environmental stimulation and how, in a recovering nervous system, this reactivity changes.

Adolescent↗

PubMed2006

Non-conscious recognition of emotional body language.

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.

Adult↗

PubMed2006

What aspects of face processing are impaired in developmental prosopagnosia?

Developmental prosopagnosia (DP) is a severe impairment in identifying faces that is present from early in life and that occurs despite no apparent brain damage and intact visual and intellectual function. Here, we investigated what aspects of face processing are impaired/spared in developmental prosopagnosia by examining a relatively large group of individuals with DP (n = 8) using an extensive battery of well-established tasks. The tasks included measures of sensitivity to global motion and to global form, detection that a stimulus is a face, determination of its sex, holistic face processing, processing of face identity based on features, contour, and the spacing of features, and judgments of attractiveness. The DP cases showed normal sensitivity to global motion and global form and performed normally on our tests of face detection and holistic processing. On the other tasks, many DP cases were impaired but there was no systematic pattern. At least half showed deficits in processing of facial identity based on either the outer contour or spacing of the internal features, and/or on judgments of attractiveness. Three of the eight were impaired in processing facial identify based on the shape of internal features. The results show that DP is a heterogeneous condition and that impairment in recognizing faces cannot be predicted by poor performance on any one measure of face processing.

Adult↗

PubMed2006

Beyond the face: exploring rapid influences of context on face processing.

Humans optimize behavior by deriving context-based expectations. Contextual data that are important for survival are extracted rapidly, using coarse information, adaptive decision strategies, and dedicated neural infrastructure. In the field of object perception, the influence of a surrounding context has been a major research theme, and it has generated a large literature. That visual context, as typically provided by natural scenes, facilitates object recognition as has been convincingly demonstrated (Bar, M. (2004) Nat. Rev. Neurosci., 5: 617-629). Just like objects, faces are generally encountered as part of a natural scene. Thus far, the facial expression literature has neglected such context and treats facial expressions as if they stand on their own. This constitutes a major gap in our knowledge. Facial expressions tend to appear in a context of head and body orientations, body movements, posture changes, and other object-related actions with a similar or at least a closely related meaning. For instance, one would expect a frightened face when confronted to an external danger to be at least accompanied by withdrawal movements of head and shoulders. Furthermore, some cues provided by the environment or the context in which a facial expression appears may have a direct relation with the emotion displayed by the face. The brain may even fill in the natural scene context typically associated with the facial expression. Recognition of the facial expression may also profit from processing the vocal emotion as well as the emotional body language that normally accompany it. Here we review the emerging evidence on how the immediate visual and auditory contexts influence the recognition of facial expressions.

Electroencephalography↗

PubMed2006

Towards the neurobiology of emotional body language.

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.

Amygdala↗

PubMed2005

Functional asymmetry and interhemispheric cooperation in the perception of emotions from facial expressions.

The present study used the redundant target paradigm on healthy subjects to investigate functional hemispheric asymmetries and interhemispheric cooperation in the perception of emotions from faces. In Experiment 1 participants responded to checkerboards presented either unilaterally to the left (LVF) or right visual half field (RVF), or simultaneously to both hemifields (BVF), while performing a pointing task for the control of eye movements. As previously reported (Miniussi et al. in J Cogn Neurosci 10:216-230, 1998), redundant stimulation led to shorter latencies for stimulus detection (bilateral gain or redundant target effect, RTE) that exceeded the limit for a probabilistic interpretation, thereby validating the pointing procedure and supporting interhemispheric cooperation. In Experiment 2 the same pointing procedure was used in a go/no-go task requiring subjects to respond when seeing a target emotional expression (happy or fearful, counterbalanced between blocks). Faster reaction times to unilateral LVF than RVF emotions, regardless of valence, indicate that the perception of positive and negative emotional faces is lateralized toward the right hemisphere. Simultaneous presentation of two congruent emotional faces, either happy or fearful, produced an RTE that cannot be explained by probability summation and suggests interhemispheric cooperation and neural summation. No such effect was present with BVF incongruent facial expressions. In Experiment 3 we studied whether the RTE for emotional faces depends on the physical identity between BVF stimuli, and we set a second BVF congruent condition in which there was only emotional but not physical or gender identity between stimuli (i.e. two different faces expressing the same emotion). The RTE and interhemispheric cooperation were present also in this second BVF congruent condition. This shows that emotional congruency is the sufficient condition for the RTE to take place in the intact brain and that the cerebral hemispheres can interact in spite of physical differences between stimuli.

Adult↗

PubMed2005

Context influences early perceptual analysis of faces--an electrophysiological study.

Electrophysiological and hemodynamic correlates of processing isolated faces have been investigated extensively over the last decade. A question not addressed thus far is whether the visual scene, which normally surrounds a face or a facial expression, has an influence on how the face is processed. Here we investigated this issue by presenting faces in natural contexts and measuring whether the emotional content of the scene influences processing of a facial expression. Event-related potentials were recorded to faces (fearful/neutral) embedded in scene contexts (fearful/neutral) while participants performed an orientation-decision task (face upright or inverted). Two additional experiments were run, one to examine the effects of context that occur without a face and the other to evaluate the effects of faces isolated from contexts. Faces without any context showed the largest N170 amplitudes. The presence of a face in a fearful context enhances the N170 amplitude over a face in neutral contexts, an effect that is strongest for fearful faces on left occipito-temporal sites. This N170 effect, and the corresponding topographic distribution, was not found for contexts-only, indicating that the increased N170 amplitude results from the combination of face and fearful context. These findings suggest that the context in which a face appears may influence how it is encoded.

Adult↗

PubMed2005

Rapid perceptual integration of facial expression and emotional body language.

In our natural world, a face is usually encountered not as an isolated object but as an integrated part of a whole body. The face and the body both normally contribute in conveying the emotional state of the individual. Here we show that observers judging a facial expression are strongly influenced by emotional body language. Photographs of fearful and angry faces and bodies were used to create face-body compound images, with either matched or mismatched emotional expressions. When face and body convey conflicting emotional information, judgment of facial expression is hampered and becomes biased toward the emotion expressed by the body. Electrical brain activity was recorded from the scalp while subjects attended to the face and judged its emotional expression. An enhancement of the occipital P1 component as early as 115 ms after presentation onset points to the existence of a rapid neural mechanism sensitive to the degree of agreement between simultaneously presented facial and bodily emotional expressions, even when the latter are unattended.

Adolescent↗

PubMed2005

Multisensory integration of emotional faces and voices in schizophrenics.

In their natural environment, organisms receive information through multiple sensory channels and these inputs from different sensory systems are routinely combined into integrated percepts. Previously, we reported that in a population of schizophrenics, deficits in audiovisual integration were observed for complex stimuli (auditory and visual syllables), but not for more simple ones (beeps and light flashes). Here, we investigated multisensory integration of emotional information in a group of schizophrenic patients. In Experiment 1, we found a reduced effect of an emotional voice on the categorization of a facial expression. In Experiment 2, the reverse test situation was presented, and, here, we observed an exaggerated effect of a face expression on the categorization of an emotional voice. Results are discussed in the light of current models of multisensory integration and their relevance for schizophrenia.

Adult↗

PubMed2005

Perception of facial expressions and voices and of their combination in the human brain.

Using positron emission tomography we explored brain regions activated during the perception of face expressions, emotional voices and combined audio-visual pairs. A convergence region situated in the left lateral temporal cortex was more activated by bimodal stimuli than by either visual only or auditory only stimuli. Separate analyses for the emotions happiness and fear revealed supplementary convergence areas situated mainly anteriorly in the left hemisphere for happy pairings and in the right hemisphere for fear pairings indicating different neuro-anatomical substrates for multisensory integration of positive versus negative emotions. Activation in the right extended amygdala was obtained for fearful faces and fearful audio-visual pairs but not for fearful voices only. These results suggest that during the multisensory perception of emotion, affective information from face and voice converge in heteromodal regions of the human brain.

Adult↗

PubMed2004

Naso-temporal asymmetry of the N170 for processing faces in normal viewers but not in developmental prosopagnosia.

Some elementary aspects of faces can be processed before cortical maturation or after lesion of primary visual cortex. Recent findings suggesting a role of an evolutionary ancient visual system in face processing have exploited the relative advantage of the temporal hemifield (nasal hemiretina). Here, we investigated whether under some circumstances face processing also shows a temporal hemifield advantage. We measured the face sensitive N170 to laterally presented faces viewed passively under monocular conditions and compared face recognition in the temporal and nasal hemiretina. A N170 response for upright faces was observed which was larger for projections to the nasal hemiretina/temporal hemifields. This pattern was not observed in a developmental prosopagnosic. These results point to the importance of the early stages of face processing for normal face recognition abilities and suggest a potentially important factor in the origins of developmental prosopagnosia.

Adult↗

PubMed2004

Fear fosters flight: a mechanism for fear contagion when perceiving emotion expressed by a whole body.

Darwin regarded emotions as predispositions to act adaptively, thereby suggesting that characteristic body movements are associated with each emotional state. To this date, investigations of emotional cognition have predominantly concentrated on processes associated with viewing facial expressions. However, expressive body movements may be just as important for understanding the neurobiology of emotional behavior. Here, we used functional MRI to clarify how the brain recognizes happiness or fear expressed by a whole body. Our results indicate that observing fearful body expressions produces increased activity in brain areas narrowly associated with emotional processes and that this emotion-related activity occurs together with activation of areas linked with representation of action and movement. The mechanism of fear contagion hereby suggested may automatically prepare the brain for action.

Adult↗

PubMed2004

The neural correlates of perceiving human bodies: an ERP study on the body-inversion effect.

The present study investigated the neural correlates of perceiving human bodies. Focussing on the N170 as an index of structural encoding, we recorded event-related potentials (ERPs) to images of bodies and faces (either neutral or expressing fear) and objects, while subjects viewed the stimuli presented either upright or inverted. The N170 was enhanced and delayed to inverted bodies and faces, but not to objects. The emotional content of faces affected the left N170, the occipito-parietal P2, and the fronto-central N2, whereas body expressions affected the frontal vertex positive potential (VPP) and a sustained fronto-central negativity (300-500 ms). Our results indicate that, like faces, bodies are processed configurally, and that within each category qualitative differences are observed for emotional as opposed to neutral images.

Adolescent↗

PubMed2004

Illusory sound shifts induced by the ventriloquist illusion evoke the mismatch negativity.

The ventriloquist illusion arises when sounds are mislocated towards a synchronous but spatially discrepant visual event. Here, we investigated the ventriloquist illusion at a neurophysiological level. The question was whether an illusory shift in sound location was reflected in the auditory mismatch negativity (MMN). An 'oddball' paradigm was used whereby simultaneously presented sounds and flashes coming from the same location served as standard. The deviant consisted of a sound originating from the same source as the standard together with a flash at 20 degrees spatial separation, which evoked an illusory sound shift. This illusory sound shift evoked an MMN closely resembling the MMN evoked by an actual sound shift. A visual-only control condition ruled out that the illusory-evoked MMN was confounded by the visual part of the audiovisual deviant. These results indicate that the crossmodal interaction on which the ventriloquist illusion is based takes place automatically at an early processing stage, within 200 ms after stimulus onset.

Acoustic Stimulation↗

PubMed2004

Recalibration of temporal order perception by exposure to audio-visual asynchrony.

The perception of simultaneity between auditory and visual information is of crucial importance for maintaining a coordinated representation of a multisensory event. Here we show that the perceptual system is able to adaptively recalibrate itself to audio-visual temporal asynchronies. Participants were exposed to a train of sounds and light flashes with a constant time lag ranging from -200 (sound first) to +200 ms (light first). Following this exposure, a temporal order judgement (TOJ) task was performed in which a sound and light were presented with a stimulus onset asynchrony (SOA) chosen from 11 values between -240 and +240 ms. Participants either judged whether the sound or the light was presented first, or whether the sound and light were presented simultaneously or successively. The point of subjective simultaneity (PSS) was, in both cases, shifted in the direction of the exposure lag, indicative of recalibration.

Acoustic Stimulation↗

PubMed2004

Haptic face recognition and prosopagnosia.

Cases of cross-modal influence have been observed since the beginning of psychological science. Yet some abilities like face recognition are traditionally only investigated in the visual domain. People with normal visual face-recognition capacities identify inverted faces more poorly than upright faces. An abnormal pattern of performance with inverted faces by prosopagnosic individuals is characteristically interpreted as evidence for a deficit in configural processing essential for normal face recognition. We investigated whether such problems are unique to vision by examining face processing by hand in a prosopagnosic individual. We used the haptic equivalent of the visual-inversion paradigm to investigate haptic face recognition. If face processing is specific to vision, our participant should not show difficulty processing faces haptically and should perform with the same ease as normal controls. Instead, we show that a prosopagnosic individual cannot haptically recognize faces. Moreover, he shows similar abnormal inversion effects by hand and eye. These results suggest that face-processing deficits can be found across different input modalities. Our findings also extend the notion of configural processing to haptic face and object recognition.

Discrimination, Psychological↗

PubMed2004

Temporal ventriloquism: sound modulates the flash-lag effect.

A sound presented in close temporal proximity to a visual stimulus can alter the perceived temporal dimensions of the visual stimulus (temporal ventriloquism). In this article, the authors demonstrate temporal ventriloquism in the flash-lag effect (FLE), a visual illusion in which a flash appears to lag relative to a moving object. In Experiment 1, the magnitude and the variability of the FLE were reduced, relative to a silent condition, when a noise burst was synchronized with the flash. In Experiment 2, the sound was presented before, at, or after the flash (+/- approximately 100 ms), and the size of the FLE varied linearly with the delay of the sound. These findings demonstrate that an isolated sound can sharpen the temporal boundaries of a flash and attract its temporal occurrence.

Auditory Perception↗