Individual differences in face cognition

Zusammenhänge zwischen neurokognitiven Indikatoren und Verhaltensindikatoren der Gesichterkognition können Gehirnsysteme und neuronale Subprozesse identifizieren, die individuellen Unterschieden im Verhalten zugrunde liegen. Diese Dissertation zeigt, dass Ereigniskorrelierte Potentiale (EKPs) als neurokognitive Indikatoren für die Erforschung individueller Unterschiede eingesetzt werden können, denn sie weisen die gleichen hohen psychometrischen Qualitäten wie andere Fähigkeitsindikatoren auf und messen daher individuelle Unterschiede in der neuronalen Verarbeitung zuverlässig und stabil über die Zeit. Auf der Verhaltensebene wurden drei Teilfähigkeiten der Gesichterkognition etabliert: Gesichterwahrnehmung, Gesichtergedächtnis und Gesichtergeschwindigkeit. EKPs wurden in Strukturgleichungsmodellen verwendet, um den Beitrag neurokognitiver Indikatoren an individuellen Unterschieden dieser Gesichterkognitionsfähigkeiten zu schätzen. Für 85 Probanden wurden Beziehungen zwischen den Gesichterkognitionsfähigkeiten und der P100, N170, der sogenannten Differenz aufgrund des Gedächtnisses (Dm) und dem frühen sowie späten Wiederholungseffekt (ERE und LRE) etabliert. Spezifische Anteile individueller Unterschiede in der Gesichterkognition auf der Verhaltensebene wurden durch individuelle Unterschiede im Zeitverlauf der strukturellen Gesichteranalyse (N170 Latenz) sowie in der Reaktivierung von Repräsentationen gespeicherter Gesichtsstrukturen (ERE) als auch personen-spezifischen Wissens (LRE) erklärt. Keinen Anteil an individuellen Unterschieden erklärten hingegen frühe Wahrnehmungsprozesse (P100), die neuronale Aktivierung während der strukturellen Gesichteranalyse (N170 Amplitude) und Prozesse der Gedächtnisenkodierung von Gesichtern (Dm). Diese Ergebnisse zeigen, dass individuelle Unterschiede in der Gesichterkognition von der strukturellen Gesichteranalyse sowie von der Effizienz und Geschwindigkeit des Zugriffs auf Gedächtnisinhalte zu Gesichtern und Personen abhängt.Individual differences in perceiving, learning, and recognizing faces were shown on the behavioral and neural level but were rarely related to one another. By determining relationships between behavioral and neurocognitive indicators of face cognition, brain systems and neural sub-processes can be identified that underlie individual variations on the behavioral level. The present dissertation laid the foundation for using event-related potentials (ERPs) as neurocognitive indicators in individual differences research. ERP components were shown to possess the same high psychometric qualities as behavioral ability measures and thus to measure individual differences of neural processing reliably and stably across time. On the behavioral level, three component abilities of face cognition were established: face perception, face memory, and the speed of face cognition. ERP components were used in structural equation models that estimated contributions of neurocognitive indicators to the individual differences in these face cognition abilities. Regression analysis was used to determine the contributions of P100, N170, the so called difference due to memory (Dm), as well as early and late repetition effects (ERE and LRE) to face cognition abilities in 85 participants. Certain amounts of variance in face cognition as seen on the behavioral level were accounted for by individual differences in the temporal dimension of structural encoding of a face (N170 latency) and in the re-activation of both stored facial structures (ERE) and person-identity information (LRE). In contrast, processes of early vision (P100), the neural activation of structural face encoding (N170 amplitude), and memory encoding of new faces (Dm) did not show any contribution to individual differences in face cognition. These findings show that individual differences in face cognition depend on the speed of structurally encoding faces and on the efficiency and speed of accessing face and person memory

Event-related potential correlates of implicit processing of own- and other-race faces in children

Human adults typically experience difficulties in recognizing and discriminating individual faces belonging to racial groups other than their own. The origin of this ‘‘other-race” effect is set in infancy, but the understanding of its developmental course is fragmented. We aimed to access the mechanisms of the other-race effect in childhood by unraveling the neural time course of ownand other-race face processing during a masked priming paradigm. White 6- and 7-year-old children (N = 19) categorized fully visible Asian (other-race) or White (own-race) target faces according to gender. Target faces were preceded by masked same-identity or different-identity prime faces, matching the target for race and gender. We showed an early priming effect on the N100 component, with larger amplitude to different-face pairs than to sameface pairs, and a later race effect on the N200 component, with larger amplitude to own-race face pairs than to other-race face pairs. Critically, race did not interact with priming at any processing stage (P100, N100, P200, N200, or P300). Our results suggest that race could have a temporally limited impact on face processing and that the implicit and unconscious identity processing of own- and other-race faces could be similar in 6- and 7-year-olds, depicting an immature other-race effect during childhood

Event-related potential correlates of implicit processing of own- and other-race faces in children

Human adults typically experience difficulties in recognizing and discriminating individual faces belonging to racial groups other than their own. The origin of this ‘‘other-race” effect is set in infancy, but the understanding of its developmental course is fragmented. We aimed to access the mechanisms of the other-race effect in childhood by unraveling the neural time course of ownand other-race face processing during a masked priming paradigm. White 6- and 7-year-old children (N = 19) categorized fully visible Asian (other-race) or White (own-race) target faces according to gender. Target faces were preceded by masked same-identity or different-identity prime faces, matching the target for race and gender. We showed an early priming effect on the N100 component, with larger amplitude to different-face pairs than to sameface pairs, and a later race effect on the N200 component, with larger amplitude to own-race face pairs than to other-race face pairs. Critically, race did not interact with priming at any processing stage (P100, N100, P200, N200, or P300). Our results suggest that race could have a temporally limited impact on face processing and that the implicit and unconscious identity processing of own- and other-race faces could be similar in 6- and 7-year-olds, depicting an immature other-race effect during childhood

Electrophysiological correlates of unconscious processes of race

The study aimed to examine the neural mechanisms underlying implicit other-race face processing by the use of the masked and unmasked priming manipulation. Two types of prime-target pairs were presented while recording Event-related potentials (ERPs): Same face pairs (prime-target were identical faces), and Different face pairs (prime-target were different faces). Prime-target pairs were half Asian (other-race) and half Caucasian (own-race) faces. The face stimuli on each pair were of the same gender and race. Participants (all Caucasians) had to decide whether the target was a male or a female face (gender task). The prime face could be unmasked or masked. On the behavioral side, our findings showed a race effect, that is slower reaction times (RTs) for other-race than own-race face stimuli, regardless of masking. On the ERPs side, our data showed a race effect across all components analyzed (P100, N100, N200, P300), under both the unmasked and masked manipulations. Besides, we found, in the unmasked condition, a priming effect as a function of race on the N100, N200, and P300 components; but, interestingly, in the masked condition, only on the P300. Overall, our findings provide evidence that race information is available very early in the brain and can strongly activate and influence people’s behaviors even without conscious awareness

Stimulus Dependency of Object-Evoked Responses in Human Visual Cortex: An Inverse Problem for Category Specificity

Many studies have linked the processing of different object categories to specific event-related potentials (ERPs) such as the face-specific N170. Despite reports showing that object-related ERPs are influenced by visual stimulus features, there is consensus that these components primarily reflect categorical aspects of the stimuli. Here, we re-investigated this idea by systematically measuring the effects of visual feature manipulations on ERP responses elicited by both structure-from-motion (SFM)-defined and luminance-defined object stimuli. SFM objects elicited a novel component at 200–250 ms (N250) over parietal and posterior temporal sites. We found, however, that the N250 amplitude was unaffected by restructuring SFM stimuli into meaningless objects based on identical visual cues. This suggests that this N250 peak was not uniquely linked to categorical aspects of the objects, but is strongly determined by visual stimulus features. We provide strong support for this hypothesis by parametrically manipulating the depth range of both SFM- and luminance-defined object stimuli and showing that the N250 evoked by SFM stimuli as well as the well-known N170 to static faces were sensitive to this manipulation. Importantly, this effect could not be attributed to compromised object categorization in low depth stimuli, confirming a strong impact of visual stimulus features on object-related ERP signals. As ERP components linked with visual categorical object perception are likely determined by multiple stimulus features, this creates an interesting inverse problem when deriving specific perceptual processes from variations in ERP components

Combined effects of inversion and feature removal on N170 responses elicited by faces and car fronts

The final publication is available at Elsevier via http://dx.doi.org/10.1016/j.bandc.2013.01.002. © 2013. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/The face-sensitive N170 is typically enhanced for inverted compared to upright faces. Itier, Alain, Sedore, and McIntosh (2007) recently suggested that this N170 inversion effect is mainly driven by the eye region which becomes salient when the face configuration is disrupted. Here we tested whether similar effects could be observed with non-face objects that are structurally similar to faces in terms of possessing a homogeneous within-class first-order feature configuration. We presented upright and inverted pictures of intact car fronts, car fronts without lights, and isolated lights, in addition to analogous face conditions. Upright cars elicited substantial N170 responses of similar amplitude to those evoked by upright faces. In strong contrast to face conditions however, the car-elicited N170 was mainly driven by the global shape rather than the presence or absence of lights, and was dramatically reduced for isolated lights. Overall, our data confirm a differential influence of the eye region in upright and inverted faces. Results for car fronts do not suggest similar interactive encoding of eye-like features and configuration for non-face objects, even when these objects possess a similar feature configuration as faces

Electrophysiological investigations of the timing of face processing

As important social stimuli, faces playa critical role in our lives. Much of our interaction with other people depends on our ability to recognize faces accurately. It has been proposed that face processing consists of different stages and interacts with other systems (Bruce & Young, 1986). At a perceptual level, the initial two stages, namely structural encoding and face recognition, are particularly relevant and are the focus of this dissertation. Event-related potentials (ERPs) are averaged EEG signals time-locked to a particular event (such as the presentation of a face). With their excellent temporal resolution, ERPs can provide important timing information about neural processes. Previous research has identified several ERP components that are especially related to face processing, including the N 170, the P2 and the N250. Their nature with respect to the stages of face processing is still unclear, and is examined in Studies 1 and 2. In Study 1, participants made gender decisions on a large set of female faces interspersed with a few male faces. The ERP responses to facial characteristics of the female faces indicated that the N 170 amplitude from each side of the head was affected by information from eye region and by facial layout: the right N 170 was affected by eye color and by face width, while the left N 170 was affected by eye size and by the relation between the sizes of the top and bottom parts of a face. In contrast, the P100 and the N250 components were largely unaffected by facial characteristics. These results thus provided direct evidence for the link between the N 170 and structural encoding of faces. In Study 2, focusing on the face recognition stage, we manipulated face identity strength by morphing individual faces to an "average" face. Participants performed a face identification task. The effect of face identity strength was found on the late P2 and the N250 components: as identity strength decreased from an individual face to the "average" face, the late P2 increased and the N250 decreased. In contrast, the P100, the N170 and the early P2 components were not affected by face identity strength. These results suggest that face recognition occurs after 200 ms, but not earlier. Finally, because faces are often associated with social information, we investigated in Study 3 how group membership might affect ERP responses to faces. After participants learned in- and out-group memberships of the face stimuli based on arbitrarily assigned nationality and university affiliation, we found that the N170 latency differentiated in-group and out-group faces, taking longer to process the latter. In comparison, without group memberships, there was no difference in N170 latency among the faces. This dissertation provides evidence that at a neural level, structural encoding of faces, indexed by the N170, occurs within 200 ms. Face recognition, indexed by the late P2 and the N250, occurs shortly afterwards between 200 and 300 ms. Social cognitive factors can also influence face processing. The effect is already evident as early as 130-200 ms at the structural encoding stage

Altering second-order configurations reduces the adaptation effects on early face-sensitive event-related potential components

The spatial distances among the features of a face are commonly referred to as second-order relations, and the coding of these properties is often regarded as a cornerstone in face recognition. Previous studies have provided mixed results regarding whether the N170, a face-sensitive component of the event-related potential, is sensitive to second-order relations. Here we investigated this issue in a gender discrimination paradigm following long-term (5 s) adaptation to normal or vertically stretched male and female faces, considering that the latter manipulation substantially alters the position of the inner facial features. Gender-ambiguous faces were more likely judged to be female following adaptation to a male face and vice versa. This aftereffect was smaller but statistically significant after being adapted to vertically stretched when compared to unstretched adapters. Event-related potential recordings revealed that adaptation effects measured on the amplitude of the N170 show strong modulations by the second-order relations of the adapter: reduced N170 amplitude was observed, however, this reduction was smaller in magnitude after being adapted to stretched when compared to unstretched faces. These findings suggest early face-processing, as reflected in the N170 component, proceeds by extracting the spatial relations of inner facial features