Coarse-to-Fine(r) Automatic Familiar Face Recognition in the Human Brain.

At what level of spatial resolution can the human brain recognize a familiar face in a crowd of strangers? Does it depend on whether one approaches or rather moves back from the crowd? To answer these questions, 16 observers viewed different unsegmented images of unfamiliar faces alternating at 6 Hz, with spatial frequency (SF) content progressively increasing (i.e., coarse-to-fine) or decreasing (fine-to-coarse) in different sequences. Variable natural images of celebrity faces every sixth stimulus generated an objective neural index of single-glanced automatic familiar face recognition (FFR) at 1 Hz in participants' electroencephalogram (EEG). For blurry images increasing in spatial resolution, the neural FFR response over occipitotemporal regions emerged abruptly with additional cues at about 6.3-8.7 cycles/head width, immediately reaching amplitude saturation. When the same images progressively decreased in resolution, the FFR response disappeared already below 12 cycles/head width, thus providing no support for a predictive coding hypothesis. Overall, these observations indicate that rapid automatic recognition of heterogenous natural views of familiar faces is achieved from coarser visual inputs than generally thought, and support a coarse-to-fine FFR dynamics in the human brain.

Critical information thresholds underlying generic and familiar face categorisation at the same face encounter.

Seeing a face in the real world provokes a host of automatic categorisations related to sex, emotion, identity, and more. Such individual facets of human face recognition have been extensively examined using overt categorisation judgements, yet their relative informational dependencies during the same face encounter are comparatively unknown. Here we used EEG to assess how increasing access to sensory input governs two ecologically relevant brain functions elicited by seeing a face: Distinguishing faces and nonfaces, and recognising people we know. Observers viewed a large set of natural images that progressively increased in either image duration (experiment 1) or spatial frequency content (experiment 2). We show that in the absence of an explicit categorisation task, the human brain requires less sensory input to categorise a stimulus as a face than it does to recognise whether that face is familiar. Moreover, where sensory thresholds for distinguishing faces/nonfaces were remarkably consistent across observers, there was high inter-individual variability in the lower informational bound for familiar face recognition, underscoring the neurofunctional distinction between these categorisation functions. By i) indexing a form of face recognition that goes beyond simple low-level differences between categories, and ii) tapping multiple recognition functions elicited by the same face encounters, the information minima we report bear high relevance to real-world face encounters, where the same stimulus is categorised along multiple dimensions at once. Thus, our finding of lower informational requirements for generic vs. familiar face recognition constitutes some of the strongest evidence to date for the intuitive notion that sensory input demands should be lower for recognising face category than face identity.

Neural microgenesis of personally familiar face recognition.

Despite a wealth of information provided by neuroimaging research, the neural basis of familiar face recognition in humans remains largely unknown. Here, we isolated the discriminative neural responses to unfamiliar and familiar faces by slowly increasing visual information (i.e., high-spatial frequencies) to progressively reveal faces of unfamiliar or personally familiar individuals. Activation in ventral occipitotemporal face-preferential regions increased with visual information, independently of long-term face familiarity. In contrast, medial temporal lobe structures (perirhinal cortex, amygdala, hippocampus) and anterior inferior temporal cortex responded abruptly when sufficient information for familiar face recognition was accumulated. These observations suggest that following detailed analysis of individual faces in core posterior areas of the face-processing network, familiar face recognition emerges categorically in medial temporal and anterior regions of the extended cortical face network.

Recognizing "Bella Swan" and "Hermione Granger": No Own-Race Advantage in Recognizing Photos of Famous Faces.

We investigated recognition of familiar and unfamiliar own- and other-race faces across natural variability in appearance. Participants sorted 20 photographs of each of two identities into piles such that each pile contained all photographs of a single identity. The other-race effect was limited to unfamiliar faces. When faces were unfamiliar, participants perceived more identities when sorting other-race faces; when faces were familiar, participants made two piles for both own- and other-race faces. Our work calls for rethinking the concept of the other-race effect.

The role of the eye region for familiar face recognition: Evidence from spatial low-pass filtering and contrast negation.

What information is used for familiar face recognition? While previous research suggests a particular importance of the eye region, information from the rest of the face also needs to be integrated. What type of information is used in conjunction with the eyes is largely unclear. In three experiments, participants were asked to recognise so-called face chimeras, in which the eye region was not manipulated, while the rest of the face was either presented in negative contrast (contrast chimeras) or low-pass filtered (blur chimeras). We show (1) that both chimeras are recognised substantially better than fully blurred faces, (2) that the recognition advantage for blur chimeras is specific to the eye region but cannot be explained by cues available in this part of the face alone, and (3) that a combination of negative contrast and blurring outside of the eye region eliminates the chimera advantage. We conclude that full-frequency but distorted surface reflectance cues (in contrast chimeras) or coarse shape information (in blur chimeras) can be used in combination with the eye region for effective face recognition. Our findings further suggest that the face recognition system can flexibly use both types of information, depending on availability.

Evaluating the Reliability and Validity of the Famous Faces Doppelgangers Test, a Novel Measure of Familiar Face Recognition.

Face recognition assessments that use images of celebrities require not only face recognition ability but also pop-culture knowledge and successful recall of identifying information. Here, we introduce a task designed to measure face recognition more specifically: the Famous Faces Doppelgangers Test (FFDT). Participants (N = 57,407) identified 40 celebrities paired with lookalike doppelgangers, allowing face recognition ability to be assessed without requiring information recall. In addition, participants reported whether they were familiar with each celebrity, allowing poor face recognition ability to be differentiated from low pop-culture knowledge. FFDT performance was reliable (rxx = .80), similar across participants of different racial and ethnic groups, and more highly correlated with memory for faces (r = .50) and self-reported face recognition ability (r = .48) than processing speed ability (r = .10). Thus, the FFDT is a reliable, valid, and specific measure of the ability to identify familiar faces, making it a promising new tool for assessing face recognition ability.

A robust neural familiar face recognition response in a dynamic (periodic) stream of unfamiliar faces.

We present an objective and sensitive approach to measure human familiar face recognition (FFR) across variable facial identities. Twenty-six participants viewed sequences of natural images of different unfamiliar faces presented at a fixed rate of 6 Hz (i.e., 6 faces by second), with variable natural images of different famous face identities appearing periodically every 7th image (i.e., .86 Hz). Participants were unaware of the goal of the study and performed an orthogonal task. Following only seven minutes of visual stimulation, the FFR response was objectively identified in the EEG spectrum at .86 Hz and its harmonics (1.71 Hz, etc.) over bilateral occipito-temporal regions, being significant in every individual participant. When the exact same images appeared upside-down, the FFR response amplitude reduced by more than 80%, and was uncorrelated across individuals to the upright face response. The FFR for upright faces emerges between 160 and 200 msec following the famous face onset over bilateral occipito-temporal region and lasts until about 560 msec. The stimulation paradigm offers an unprecedented way to characterize rapid and automatic human face familiarity recognition across individuals, during development and clinical conditions, also providing original information about the time-course and neural basis of human FFR in temporally constrained stimulation conditions with natural images.

Eye see through you! Eye tracking unmasks concealed face recognition despite countermeasures.

BACKGROUND: Criminal associates such as terrorist members are likely to deny knowing members of their network when questioned by police. Eye tracking research suggests that lies about familiar faces can be detected by distinct markers of recognition (e.g. fewer fixations and longer fixation durations) across multiple eye fixation parameters. However, the effect of explicit eye movement strategies to concealed recognition on such markers has not been examined. Our aim was to assess the impact of fixed-sequence eye movement strategies (across the forehead, ears, eyes, nose, mouth and chin) on markers of familiar face recognition. Participants were assigned to one of two groups: a standard guilty group who were simply instructed to conceal knowledge but with no specific instructions on how to do so; and a countermeasures group who were instructed to look at every familiar and unfamiliar face in the same way by executing a consistent sequence of fixations. RESULTS: In the standard guilty group, lies about recognition of familiar faces showed longer average fixation durations, a lower proportion of fixations to the inner face regions, and proportionately more viewing of the eyes than honest responses to genuinely unknown faces. In the countermeasures condition, familiar face recognition was detected by longer fixations durations, fewer fixations to the inner regions of the face, and fewer interest areas of the face viewed. Longer fixation durations were a consistent marker of recognition across both conditions for most participants; differences were detectable from the first fixation. CONCLUSION: The results suggest that individuals can exert a degree of executive control over fixation patterns but that: the eyes are particularly attention-grabbing for familiar faces; the more viewers look around the face, the more they give themselves away; and attempts to deploy the same fixation patterns to familiar and unfamiliar faces were unsuccessful. The results suggest that the best strategy for concealing recognition might be to keep the eyes fixated in the centre of the screen but, even then, recognition is apparent in longer fixation durations. We discuss potential optimal conditions for detecting concealed knowledge of faces.

Revisiting the earliest electrophysiological correlate of familiar face recognition.

The present study used event-related potentials (ERPs) to reinvestigate the earliest face familiarity effect (FFE: ERP differences between familiar and unfamiliar faces) that genuinely reflects cognitive processes underlying recognition of familiar faces in long-term memory. To trigger relatively early FFEs, participants were required to categorize upright and inverted famous faces and unknown faces in a task that placed high demand on face recognition. More importantly, to determine whether an observed FFE was linked to on-line face recognition, systematical investigation about the relationship between the FFE and behavioral performance of face recognition was conducted. The results showed significant FFEs on P1, N170, N250, and P300 waves. The FFEs on occipital P1 and N170 (<200ms) showed reversed polarities for upright and inverted faces, and were not correlated with any behavioral measure (accuracy, response time) or modulated by learning, indicating that they might merely reflect low-level visual differences between face sets. In contrast, the later FFEs on occipito-temporal N250 (~230ms) and centro-parietal P300 (~350ms) showed consistent polarities for upright and inverted faces. The N250 FFE was individually correlated with recognition speed for upright faces, and could be obtained for inverted faces through learning. The P300 FFE was also related to behavior in many aspects. These findings provide novel evidence supporting that cognitive discrimination of familiar and unfamiliar faces starts no less than 200ms after stimulus onset, and the familiarity effect on N250 may be the first electrophysiological correlate underlying recognition of familiar faces in long-term memory.

Facilitated detection of social cues conveyed by familiar faces.

Recognition of the identity of familiar faces in conditions with poor visibility or over large changes in head angle, lighting and partial occlusion is far more accurate than recognition of unfamiliar faces in similar conditions. Here we used a visual search paradigm to test if one class of social cues transmitted by faces-direction of another's attention as conveyed by gaze direction and head orientation-is perceived more rapidly in personally familiar faces than in unfamiliar faces. We found a strong effect of familiarity on the detection of these social cues, suggesting that the times to process these signals in familiar faces are markedly faster than the corresponding processing times for unfamiliar faces. In the light of these new data, hypotheses on the organization of the visual system for processing faces are formulated and discussed.