Biomedical subjects

Stefan R Schweinberger

Publications and source records attributed to Stefan R Schweinberger.

At least 19 recordsLinked to original sources

PubMed2006

Hemispheric asymmetries in font-specific and abstractive priming of written personal names: Evidence from event-related brain potentials.

We assessed hemispheric differences in font-specific and abstractive repetition priming for famous persons' names. Participants performed speeded familiarity judgments for foveally presented famous and unfamiliar names. Famous target names were preceded by primes (150 ms) in the left or right visual field (LVF or RVF). Primes were either the same name as the target written in the same font (font-specific priming), the same name in a different font (abstractive priming), or a different name (unprimed condition). In reaction times, LH superiority was strong for abstractive priming across fonts, but was reduced to insignificance for font-specific priming. We observed 3 different ERP modulations of priming for target names: a small font-specific posterior N200 (160-220 ms), a left temporal N250r (220-300 ms), and an N400 modulation (300-500 ms). The left temporal N250r exhibited large and abstractive priming for RVF primes, but smaller and font-specific priming for LVF primes. N400 effects were observed in all priming conditions. With respect to previous findings that N200, N250r, and N400 reflect facilitation at the levels of font-specific encoding, lexical entries for names, and semantic processing, respectively, these findings suggest that the LH superiority for name processing is particularly pronounced for the access to abstractive lexical entries for written names, a process that may be mediated by the left fusiform cortex.

Adolescent↗

PubMed2006

Masked and unmasked electrophysiological repetition effects of famous faces.

We investigated immediate repetition effects of sequentially presented famous face pairs. The first face (F1) was presented masked or unmasked and preceded the second face (F2) with different SOAs (84 ms vs. 500 ms). Participants judged F2 with regard to either semantic category (actor vs. singer; indirect task) or perceptual match with F1 (same vs. different; direct task). Repetition shortened RT for unmasked but not for masked F1 conditions. In event-related brain potentials (ERPs), unmasked repetition effects were influenced by task and SOA and consisted a modulation of an occipitotemporal N170, an inferior temporal N250r (200-300 ms), a central-parietal N400 (300-500 ms), and a parietal P600 (500-800 ms). An early occipital negativity (onset approximately 100 ms) was present at the 84-ms SOA but diminished in the 500-ms SOA condition, probably reflecting a fast decaying iconic memory trace. Masked repetition effects in the indirect task were limited to a significant early (100-150 ms) prefrontal/lateral frontal and central-parietal modulation, and a strong trend for a reduced N170 amplitude. This suggests that masked repetition modulated early visual processing but did not influence processes beyond approximately 200 ms that reflect the access to facial representations and semantic information for people.

Adolescent↗

PubMed2006

Effects of personal familiarity on early neuromagnetic correlates of face perception.

This study investigated effects of familiarity and orientation on face processing by means of magnetoencephalography. Participants were presented with photographs of personally familiar, famous and unfamiliar faces in both upright and inverted orientation. They had to decide whether faces were familiar by means of manual yes/no responses. Independent of orientation, we observed a clear modulation of the M170 by familiarity, with personally familiar faces evoking larger amplitudes than unknown faces. The M170 was also sensitive to orientation, with larger amplitudes for inverted than upright faces. Moreover, the M170 exhibited larger amplitudes over the right than over the left hemisphere, but this asymmetry was present for upright faces only. The present data suggest that at least for personally familiar faces, neural correlates of identification start no later than approximately 170 ms, and underline a special role of the right hemisphere for faces in their typical upright orientation.

Adult↗

PubMed2005

The Thatcher illusion seen by the brain: an event-related brain potentials study.

In "Thatcherized" faces, the eyes and mouth regions are turned upside-down. Only when presented upright they are perceived as severely distorted. Common theories explain this effect by the loss of configural information for inverted faces. We investigated neural correlates of Thatcherization using event related potentials (ERPs). Sixteen right-handed participants performed identity classifications on Thatcherized or original familiar faces, presented either for 34 ms or 200 ms at an orientation of either 0 degrees, 90 degrees or 180 degrees. For the occipito-temporal N170, we found (1) strong non-linear effects of orientation and (2) interactions between Thatcherization and orientation: Thatcherization resulted in larger N170 for upright faces, but smaller N170 for inverted faces. The novel finding of N170 effects of Thatcherization in inverted faces suggests differences in the neural encoding of Thatcherized and original inverted faces, even though Thatcherization escapes subjective perception in inverted faces.

Adolescent↗

PubMed2005

Speaker variations influence speechreading speed for dynamic faces.

We investigated the influence of task-irrelevant speaker variations on speechreading performance. In three experiments with video digitised faces presented either in dynamic, static-sequential, or static mode, participants performed speeded classifications on vowel utterances (German vowels /u/ and /i/). A Garner interference paradigm was used, in which speaker identity was task-irrelevant but could be either correlated, constant, or orthogonal to the vowel uttered. Reaction times for facial speech classifications were slowed by task-irrelevant speaker variations for dynamic stimuli. The results are discussed with reference to distributed models of face perception (Haxby et al, 2000 Trends in Cognitive Sciences 4 223-233) and the relevance of both dynamic information and speaker characteristics for speechreading.

Adult↗

PubMed2004

N250r: a face-selective brain response to stimulus repetitions.

We investigated event-related brain potentials elicited by repetitions of cars, ape faces, and upright and inverted human faces. A face-selective N250r response to repetitions emerged over right temporal regions, consistent with a source in the fusiform gyrus. N250r was largest for human faces, clear for ape faces, non-significant for inverted faces, and completely absent for cars. Our results suggest that face-selective neural activity starting at 200 ms and peaking at 250-300 ms is sensitive to repetition and relates to individual recognition.

Adolescent↗

PubMed2004

Face repetition effects in direct and indirect tasks: an event-related brain potentials study.

We investigated immediate repetition effects on event-related potentials (ERPs) during direct and indirect tasks for sequentially presented face pairs. The first face (F1) was presented masked or unmasked, and at different stimulus onset asynchronies (SOAs, 67 vs. 1000 ms) preceding the second face (F2). Experiment I (indirect task) required a semantic classification of F2, with F1 identity being irrelevant. Experiment II (direct task) used the same stimulus sequence but required a physical identity matching of F1 and F2. Whereas no masked repetition effects in behaviour or ERPs were seen, such effects were clearly shown for unmasked F1 faces. For short SOAs, an early-onset ( approximately 100 ms) occipital repetition effect, an inferior temporal N250r (200-300 ms) and a central-parietal N400 modulation (300-500 ms) were seen in both tasks, whereas a parietal P600 effect (500-800 ms) was only present in the indirect task. For long SOAs, the early occipital effect disappeared, suggesting that it reflects a fast decaying iconic memory trace. Clear task differences were seen for N250r, N400, and P600 modulations: P600 was larger for the indirect task, and may be a correlate of semantic analysis required by this task. By contrast, N250r and N400 were larger for the direct task, suggesting that these components are sensitive to task relevance and/or attentional focus to F1, and thus do not reflect purely automatic facilitation in processing. This suggests an influence of strategic processing on the activation of both perceptual representations of faces and semantic representations of people.

Adolescent↗

PubMed2004

Expression influences the recognition of familiar faces.

Face recognition has been assumed to be independent of facial expression. We used familiar and unfamiliar faces that were morphed from a happy to an angry expression within a given identity. Participants performed speeded two-choice decisions according to whether or not a face was familiar. Consistent with earlier findings, reaction times for classifications of unfamiliar faces were independent of facial expressions. In contrast, expression clearly influenced the recognition of familiar faces. with fastest recognition for moderately happy expressions. This suggests that representations of familiar faces for recognition preserve some information about typical emotional expressions.

Adult↗

PubMed2004

What's special about personally familiar faces? A multimodal approach.

Dual-route models of face recognition suggest separate cognitive and affective routes. The predictions of these models were assessed in recognition tasks with unfamiliar, famous, and personally familiar faces. Whereas larger autonomic responses were only triggered for personally familiar faces, priming effects in reaction times to these faces, presumably reflecting cognitive recognition processes, were equal to those of famous faces. Activation of stored structural representations of familiar faces (face recognition units) was assessed by recording the N250r component in event-related brain potentials. Face recognition unit activation increased from unfamiliar over famous to personally familiar faces, suggesting that there are stronger representations for personally familiar than for famous faces. Because the topographies of the N250r for personally and famous faces were indistinguishable, a similar network of face recognition units can be assumed for both types of faces.

Adult↗

PubMed2003

A principled method for determining the functionality of brain responses.

A challenging issue in relating brain function to perception and cognition concerns the functional interpretation of brain responses. For example, while there is agreement that the N170 component of event-related potentials is sensitive to face processing, there is considerable debate about whether its response reflects a structural encoder for faces, a feature (e.g. eye) detector, or something else. We introduce a principled approach to determine the stimulus features driving brain responses. Our analyses on two observers resolving different face categorization tasks (gender and expressive or not) reveal that the N170 responds to the eyes within a face irrespective of task demands. This suggests a new methodology to attribute function to different components of the neural system for perceiving complex stimuli.

Brain↗

PubMed2003

Neural correlates of shape from shading.

Psychophysical studies have shown that human observers resolve shape-from-shading ambiguities by assuming that light is coming from above-left. Using event-related potentials (ERPs), we measured the processing time of the perception of an ambiguous shaded pattern. We found that the N2 component followed the change of perceived shape with stimulus orientation. We also found that the P1 component in occipital and temporal areas was correlated with the observers' idiosyncratic bias for light source position. The precocity of the correlated ERP components suggests that the light source is represented early in the visual system. Altogether, our results indicate that shape-from-shading is a mostly bottom-up mechanism.

Adult↗

PubMed2003

Covert recognition and the neural system for face processing.

In this viewpoint, we discuss the new evidence on covert face recognition in prosopagnosia presented by Bobes et al. (2003, this issue) and by Sperber and Spinnler (2003, this issue). Contrary to earlier hypotheses, both papers agree that covert and overt face recognition are based on the same mechanism. In line with this suggestion, an analysis of reported cases with prosopagnosia indicates that a degree of successful encoding of facial representations is a prerequisite for covert recognition to occur. While we agree with this general conclusion as far as Bobes et al.'s and Sperber and Spinnler's data are concerned, we also discuss evidence for a dissociation between different measures of covert recognition. Specifically, studies in patients with Capgras delusion and patients with prosopagnosia suggest that skin conductance and behavioural indexes of covert face recognition are mediated by partially different mechanisms. We also discuss implications of the new data for models of normal face recognition that have been successful in simulating covert recognition phenomena (e.g., Young and Burton, 1999, and O'Reilly et al., 1999). Finally, in reviewing recent neurophysiological and brain imaging evidence concerning the neural system for face processing, we argue that the relationship between ERP components (specifically, N170, N250r, and N400) and different cognitive processes in face recognition is beginning to emerge.

Brain↗

PubMed2003

Interhemispheric cooperation for face recognition but not for affective facial expressions.

Interhemispheric cooperation can be indicated by enhanced performance when stimuli are presented to both visual fields relative to one visual field alone. This "bilateral gain" is seen for words but not pseudowords in lexical decision tasks, and has been attributed to the operation of interhemispheric cell assemblies that exist only for meaningful words with acquired cortical representations. Recently, a bilateral gain has been reported for famous but not unfamiliar faces in a face recognition task [Neuropsychologia 40 (2002) 1841]. In Experiment 1 of the present paper, participants performed familiarity decisions for faces that were presented to the left (LVF), the right (RVF), or to both visual fields (BVF). An advantage for BVF relative to both LVF and RVF stimuli was seen in reaction times (RTs) to famous faces, but this bilateral advantage was absent for unfamiliar faces. In Experiment 2, participants classified the expression (happy or neutral) of unfamiliar faces. No bilateral advantage was seen for expressions, although a right hemisphere superiority was seen in terms of higher accuracy for LVF and BVF trials relative to the RVF. Recognition of famous faces (but not of facial expressions) require access to acquired memory representations that may be instantiated via cortical cell assemblies, and it is suggested that interhemispheric cooperation depends on these acquired cortical representations.

Adolescent↗

PubMed2003

Matching faces for semantic information and names: an event-related brain potentials study.

In face identification, it has been controversial whether or not access to biographical information and to a person's name are mediated by qualitatively different loci. We recorded ERPs while participants saw two successive faces and performed a matching task that either required retrieval of semantic information ("same or different profession?"), or retrieval of the person's name ("same or different number of forename syllables?"). For both tasks, slow ERP activity between the first and the second face was characterized by a prominent right posterior negativity, with the asymmetry being larger for the name than the semantic matching task. ERPs to the second face showed a difference between congruent (matching) and incongruent (mismatching) trials, with more negative ERPs for incongruent trials. In the semantic matching task, these differences were significant between 450 and 550 ms, and resembled an N400, with a maximum negativity over the vertex. In the name matching task, the topography of this congruency effect was qualitatively different from that seen in semantic matching. These findings suggest that different brain substrates mediate the access to semantic and name information.

Adolescent↗

PubMed2003

N200, N250r, and N400 event-related brain potentials reveal three loci of repetition priming for familiar names.

The authors assessed immediate repetition effects on event-related potentials (ERPs) while participants performed familiarity decisions for written personal names. For immediately repeated familiar names, the authors observed 3 distinct ERP modulations. At 180-220 ms, a posterior N200 effect occurred for names preceded by same-font primes only. In addition, an increased left temporal negativity (N250r, 220-300 ms) and a reduced central-parietal negativity (N400, 300-400 ms) were seen both for same-font and different-font repetitions. In a 2nd experiment, when names were preceded by either their corresponding face or the face of a different celebrity, only the N400 effect was preserved. These findings suggest that the N200, N250r, and N400 effects reflect facilitated processing at font-specific featural, lexical, and semantic levels of processing, respectively.

Adolescent↗

PubMed2002

Personal names and the human right hemisphere: an illusory link?

Names are thought to be represented in the brain differently from common nouns. Although this idea is supported by both theoretical and empirical arguments, the brain areas that are relevant for the recognition of personal names-and in particular the extent of right hemisphere involvement-remain controversial. We investigated the hypothesis that, unlike common nouns, personal names are represented preferentially by the right hemisphere (D. Van Lancker, 1991; D. Van Lancker et al., 1991; C. Ohnesorge & D. Van Lancker, 1999). Participants performed lexical decisions to common nouns and pseudowords (Experiment 1) or familiarity decisions to personal names (Experiment 2), which were presented briefly to the left or right visual fields. Asymmetries were small or absent for both pseudowords and unfamiliar names. For familiar names, both reaction times and error rates revealed strong advantages for the right visual field/left hemisphere (RVF/LH), which were comparable to the asymmetries for nouns. Familiar personal names may be represented by brain systems that differ from those representing common nouns, but current evidence does not suggest a distinct contribution of the right hemisphere to these brain systems.

Adult↗

PubMed2002

Interhemispheric cooperation for familiar but not unfamiliar face processing.

Evidence for interhemispheric cooperation during language processing has been demonstrated for words, but not for meaningless pseudowords. Specifically, responses were found to be faster and more accurate when identical copies of a word were presented bilaterally to both hemispheres, relative to unilateral single presentations. This bilateral advantage for words seems to be a robust effect in normals. The present study addressed the question of whether the bilateral advantage is restricted to lexical material or whether it is a more global phenomenon occurring for meaningful material in general. Thirty healthy participants performed a familiarity decision in which one copy of familiar and unfamiliar faces was presented tachistoscopically to the right visual hemifield (RVF), the left visual hemifield (LVF) or simultaneously to both visual hemifields (bilateral condition, BVF). We obtained a highly significant familiarity by visual field interaction(P < 0.006) showing that only for familiar faces, a bilateral advantage was obtained. Unfamiliar face processing did not yield a bilateral advantage. We conclude that interhemispheric cooperation only occurs for meaningful material for which cortical representations can be assumed.

Adult↗

PubMed2002

Human brain potential correlates of repetition priming in face and name recognition.

We investigated repetition priming in the recognition of famous people by recording event-related brain potentials (ERPs) and reaction times (RTs). Participants performed speeded two-choice responses depending on whether or not a stimulus showed a famous person. In Experiment 1, a facilitation was found in RTs to famous (but not to unfamiliar) faces when primed by the same face shown in an earlier priming phase of the experiment. In ERPs, an influence of repetition priming was observed neither for the N170 nor for a temporal N250 component which in previous studies had been shown to be sensitive to immediate face repetitions. ERPs to primed unfamiliar faces were more negative over right occipitotemporal areas than those to unprimed faces, but this effect was specific for repetitions of the same image, consistent with recent findings. In contrast, ERPs to primed familiar faces were more positive than those to unprimed faces at parietal sites from 500-600 ms after face onset, and these priming effects were comparable regardless of whether the same or a different image of the celebrity had served as prime. In Experiment 2, similar results were found for name recognition-a facilitation in RTs to primed familiar but not unfamiliar names, and a parietal positivity to primed names around 500-600 ms. ERP repetition effects showed comparable topographies for faces and names, consistent with the idea of a common underlying source. With reference to current models of face recognition, we suggest that these ERP repetition effects for familiar stimuli reflect a change in post-perceptual representations for people, rather than a neural correlate of recognition at a perceptual level.

Adolescent↗