An event-related brain potential study of explicit face recognition

To determine the time course of face recognition and its links to face-sensitive event-related potential (ERP) components, ERPs elicited by faces of famous individuals and ERPs to non-famous control faces were compared in a task that required explicit judgements of facial identity. As expected, the face-selective N170 component was unaffected by the difference between famous and non-famous faces. In contrast, the occipito-temporal N250 component was linked to face recognition, as it was selectively triggered by famous faces. Importantly, this component was present for famous faces that were judged to be definitely known relative to famous faces that just appeared familiar, demonstrating that it is associated with the explicit identification of a particular face. The N250 is likely to reflect early perceptual stages of face recognition where long-term memory traces of familiar faces in ventral visual cortex are activated by matching on-line face representations. Famous faces also triggered a broadly distributed longer-latency positivity (P600f) that showed a left-hemisphere bias and was larger for definitely known faces, suggesting links between this component and name generation. These results show that successful face recognition is predicted by ERP components over face-specific visual areas that emerge within 230 ms after stimulus onset.     

A new selective developmental deficit: Impaired object recognition with normal face recognition

Introduction

Studies of developmental deficits in face recognition, or developmental prosopagnosia, have shown that individuals who have not suffered brain damage can show face recognition impairments coupled with normal object recognition ( [Duchaine and Nakayama, 2005] , [Duchaine et?al., 2006] and [Nunn et?al., 2001] ). However, no developmental cases with the opposite dissociation – normal face recognition with impaired object recognition – have been reported. The existence of a case of non-face developmental visual agnosia would indicate that the development of normal face recognition mechanisms does not rely on the development of normal object recognition mechanisms.

Methods

To see whether a developmental variant of non-face visual object agnosia exists, we conducted a series of web-based object and face recognition tests to screen for individuals showing object recognition memory impairments but not face recognition impairments. Through this screening process, we identified AW, an otherwise normal 19-year-old female, who was then tested in the lab on face and object recognition tests.

Results

AW’s performance was impaired in within-class visual recognition memory across six different visual categories (guns, horses, scenes, tools, doors, and cars). In contrast, she scored normally on seven tests of face recognition, tests of memory for two other object categories (houses and glasses), and tests of recall memory for visual shapes. Testing confirmed that her impairment was not related to a general deficit in lower-level perception, object perception, basic-level recognition, or memory.

Discussion

AW’s results provide the first neuropsychological evidence that recognition memory for non-face visual object categories can be selectively impaired in individuals without brain damage or other memory impairment. These results indicate that the development of recognition memory for faces does not depend on intact object recognition memory and provide further evidence for category-specific dissociations in visual recognition.     

The role of face shape and pigmentation in other-race face perception: An electrophysiological study

Adult observers generally find it difficult to recognize and distinguish faces that belong to categories with which they have limited visual experience. One aspect of this phenomenon is commonly known as the “Other-Race Effect” (ORE) since this behavior is typically highly evident in the perception of faces belonging to ethnic or racial groups other than that of the observer. This acquired disadvantage in face recognition likely results from highly specific “tuning” of the underlying representation of facial appearance, leading to efficient processing of commonly seen faces at the expense of poor generalization to other face categories. In the current study we used electrophysiological (event-related potentials or ERPs) and behavioral measures of performance to characterize face processing in racial categories defined by dissociable shape and pigmentation information. Our goal was to examine the specificity of the representation of facial appearance in more detail by investigating how race-specific face shape and pigmentation separately modulated neural responses previously implicated in face processing, the N170 and N250 components. We found that both components were modulated by skin color, independent of face shape, but that only the N250 exhibited sensitivity to face shape. Moreover, the N250 appears to only respond differentially to the skin color of upright faces, showing a lack of color sensitivity for inverted faces.     

The fusiform face area is not sufficient for face recognition: evidence from a patient with dense prosopagnosia and no occipital face area

We tested functional activation for faces in patient D.F., who following acquired brain damage has a profound deficit in object recognition based on form (visual form agnosia) and also prosopagnosia that is undocumented to date. Functional imaging demonstrated that like our control observers, D.F. shows significantly more activation when passively viewing face compared to scene images in an area that is consistent with the fusiform face area (FFA) (p < 0.01). Control observers also show occipital face area (OFA) activation; however, whereas D.F.'s lesions appear to overlap the OFA bilaterally. We asked, given that D.F. shows FFA activation for faces, to what extent is she able to recognize faces? D.F. demonstrated a severe impairment in higher level face processing--she could not recognize face identity, gender or emotional expression. In contrast, she performed relatively normally on many face categorization tasks. D.F. can differentiate faces from non-faces given sufficient texture information and processing time, and she can do this is independent of color and illumination information. D.F. can use configural information for categorizing faces when they are presented in an upright but not a sideways orientation and given that she also cannot discriminate half-faces she may rely on a spatially symmetric feature arrangement. Faces appear to be a unique category, which she can classify even when she has no advance knowledge that she will be shown face images. Together, these imaging and behavioral data support the importance of the integrity of a complex network of regions for face identification, including more than just the FFA--in particular the OFA, a region believed to be associated with low-level processing.     

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.     

The classification of 'fear' from faces is associated with face recognition skill in women.

Two experiments were conducted to explore the relationship between the discrimination of the facial expression of 'fear' in faces and facial recognition. On the basis of the reported role of the amygdala in both processes in patients, we hypothesised that the two skills would be correlated in normal adults. In Experiment 1, a series of tests of facial expression categorisation, of face matching and of familiar and unfamiliar face recognition was conducted on normal young women, for whom psychometric scores were also obtained (n=23). Accuracy of categorisation of fear from faces predicted variance in face recognition accuracy-especially in tasks of unfamiliar face recognition (immediate old-new discrimination). No other correlations between face processing and expression classification were significant. Experiment 2 repeated the expression classification tests and an unfamiliar face recognition test on a new sample of men (n=13) and women (n=16). While there were no sex differences in face recognition, the correlation between 'fear' and face recognition was replicated only for women. These data indicate that the amygdala supports both the specific apprehension of fear in faces and face recognition in adult human females, but that the association may not hold for men. Sex differences in the structure of the amygdala-hippocampal complex suggest a likely cortical substrate for the observed differences. We speculate that social learning, which involves identifying the faces of potentially salient others, and also their attitude to the observer, engages the amygdala more readily in women than in men.     

A test movie to study elementary abilities in perception and recognition of mimic and gestural expression

Summary A test movie consisting of 13 different silent movie scenes, each 10s in duration, was developed to test in patients the elementary abilities, perception and recognition of mimic and gestural expression. Each scene was subjected to 10 (2×5) verbal or non-verbal multiple-choice tests. Quantitative analysis of normal control group results is described. All sub-tests were very easy for normals and resulted in error scores below 5%. Thus the test is not designed to differentiate within a group of normal subjects but to characterize a pathological reduction in mimic, gesture and person recognition in schizophrenic and brain-lesioned patients.By measuring the dependency of correct recognition of the different movie scenes on the inspection duration, it was shown that the projection time of 10s applied in the full test led to a fairly high amount of informational redundancy. This was intentional so that stimulus material could be well perceived and recognized even by patients with somewhat fluctuating attentiveness.     

Autistic traits are linked to reduced adaptive coding of face identity and selectively poorer face recognition in men but not women

Our ability to discriminate and recognize thousands of faces despite their similarity as visual patterns relies on adaptive, norm-based, coding mechanisms that are continuously updated by experience. Reduced adaptive coding of face identity has been proposed as a neurocognitive endophenotype for autism, because it is found in autism and in relatives of individuals with autism. Autistic traits can also extend continuously into the general population, raising the possibility that reduced adaptive coding of face identity may be more generally associated with autistic traits. In the present study, we investigated whether adaptive coding of face identity decreases as autistic traits increase in an undergraduate population. Adaptive coding was measured using face identity aftereffects, and autistic traits were measured using the Autism-Spectrum Quotient (AQ) and its subscales. We also measured face and car recognition ability to determine whether autistic traits are selectively related to face recognition difficulties. We found that men who scored higher on levels of autistic traits related to social interaction had reduced adaptive coding of face identity. This result is consistent with the idea that atypical adaptive face-coding mechanisms are an endophenotype for autism. Autistic traits were also linked with face-selective recognition difficulties in men. However, there were some unexpected sex differences. In women, autistic traits were linked positively, rather than negatively, with adaptive coding of identity, and were unrelated to face-selective recognition difficulties. These sex differences indicate that autistic traits can have different neurocognitive correlates in men and women and raise the intriguing possibility that endophenotypes of autism can differ in males and females.     

The other face of the other-race effect: an fMRI investigation of the other-race face categorization advantage

The present study was the first to use the functional magnetic resonance imaging (fMRI) methodology to investigate the neural correlates of race categorization of own- and other-race faces. We found that Chinese participants categorized the race of Caucasian faces more accurately and faster than that of Chinese faces, replicating the robust effect of the other-race categorization advantage. Regions of interest (ROI) analyses revealed greater neural activations when participants were categorizing own-race faces than other-race faces in the bilateral ventral occipito-temporal cortex (VOT) such as the fusiform face areas (FFAs) and the occipital face areas (OFAs). Within the left FFA, there was also a significant negative correlation between the behavioral difference of own- and other-race face categorization accuracy and the activation difference between categorizing own- and other-race faces. Whole brain analyses showed that categorizing own-race faces induced greater activations in the right medial frontal cortex (MFC) and right inferior frontal gyrus (IFG) than categorizing other-race faces. Psychophysiological interaction (PPI) analyses revealed that the frontal cortical regions interacted more strongly with the posterior VOT during the categorization of own-race faces than that of other-race faces. Overall, our findings suggest that relative to the categorization of other-race faces, more cortical resources are engaged during the categorization of own-race faces with which we have a higher level of processing expertise. This increased involvement of cortical neural sources perhaps serves to provide more in-depth processing of own-race faces (such as individuation), which in turn paradoxically results in the behavioral other-race categorization advantage.     

The Cambridge Face Memory Test: results for neurologically intact individuals and an investigation of its validity using inverted face stimuli and prosopagnosic participants

The two standardized tests of face recognition that are widely used suffer from serious shortcomings [Duchaine, B. & Weidenfeld, A. (2003). An evaluation of two commonly used tests of unfamiliar face recognition. Neuropsychologia, 41, 713-720; Duchaine, B. & Nakayama, K. (2004). Developmental prosopagnosia and the Benton Facial Recognition Test. Neurology, 62, 1219-1220]. Images in the Warrington Recognition Memory for Faces test include substantial non-facial information, and the simultaneous presentation of faces in the Benton Facial Recognition Test allows feature matching. Here, we present results from a new test, the Cambridge Face Memory Test, which builds on the strengths of the previous tests. In the test, participants are introduced to six target faces, and then they are tested with forced choice items consisting of three faces, one of which is a target. For each target face, three test items contain views identical to those studied in the introduction, five present novel views, and four present novel views with noise. There are a total of 72 items, and 50 controls averaged 58. To determine whether the test requires the special mechanisms used to recognize upright faces, we conducted two experiments. We predicted that controls would perform much more poorly when the face images are inverted, and as predicted, inverted performance was much worse with a mean of 42. Next we assessed whether eight prosopagnosics would perform poorly on the upright version. The prosopagnosic mean was 37, and six prosopagnosics scored outside the normal range. In contrast, the Warrington test and the Benton test failed to classify a majority of the prosopagnosics as impaired. These results indicate that the new test effectively assesses face recognition across a wide range of abilities.     

Comparative studies on recognition of faces,mimic and gestures in adolescent and middle-aged schizophrenic patients

Summary In adolescent and middle-aged schizophrenic patients and normals 10 different multiple-choice tests of 12 scored movie scenes lasting 10 s were applied, measuring the ability to recognize faces, persons and mimic expressions. In all tests errors were significantly higher by a factor of 7 to 14 in patients as compared to normals. The relative impairment of adolescent schizophrenic patients (as compared to adolescent normals) was somewhat stronger than that of adult schizophrenics. This supports the hypothesis that the impairment found in schizophrenic patients is caused by the disease and not by other factors such as duration of illness or hospitalization.     

Hippocampal underactivation in an fMRI study of word and face memory recognition in schizophrenia

Schizophrenia is a major mental disorder which is characterized by several cognitive deficits. Investigations of the neural basis of memory dysfunctions using neuroimaging techniques suggest that the hippocampus plays an important role in declarative memory impairment. The goal of this study was to investigate possible dysfunctions in cerebral activation in schizophrenic patients during both word and face recognition memory tasks. We tested 22 schizophrenics and 24 controls matched by gender, age, handedness and parental socioeconomic status. Compared to healthy volunteers, patients with schizophrenia showed decreased bilateral hippocampal activation during word and face recognition tasks. The whole brain analysis also showed a pattern of cortical and subcortical hypoactivation for both verbal and non-verbal recognition. This study provides further evidence of hippocampal involvement in declarative memory impairments of schizophrenia.     

Who is who: Italian norms for visual recognition and identification of celebrities

Abstract Age-, education- and sex-adjusted norms are provided for two new neuropsychological tests, namely (i) Face Recognition (guess of familiarity) and (ii) Person Identification (biographical contextualisation). Sixty-three pictures of celebrities and 63 of unknown people were selected following two interwoven criteria¹: the realm of their celebrity (i. e., entertainment, culture and politics) and the period of celebrity acquisition (i. e., pre-war, post-war and contemporary). Both media- and education-dependent knowledge of celebrity were considered. Ninety-eight unpaid healthy participants aged between 50 and 93 years and with at least 8 years of formal education took part in this study. Reference is made to serial models of familiar face/persons processing. Recognition is held to tackle the activity of Personal Identity Nodes (PINs) and identification of the Exemplar Semantics Archives. Given the seriality of the reference model, the Identification Test is embedded in the Recognition test. This entailed that only previously recognised faces were employed to achieve norms for identification. Note As the collaboration of each author was essential for the study, following our normal practice, names have been listed in alphabetical order. I.B. and H.S. proposed the study. F.F. and S.P. collected the data. C.S. carried out the statistical analyses. I.B. collaborated with H.S. in writing the text. ¹Authors can provide on request the CD-ROM with the face stimuli (Fig. 2 in this paper) and the blank protocols for running the two tests at issue. An erratum to this article can be found at .     

The role of lateral occipital face and object areas in the face inversion effect

Stimulus inversion impairs face discrimination to a greater extent than discrimination of other non-face object categories. This finding has led to suggestions that upright faces are represented by mechanisms specialized for upright faces whereas inverted face representation depends on more general object recognition mechanisms. In the present study we tested the causal role of face-selective and object-selective cortical areas for upright and inverted face discrimination by transiently disrupting neural processing using transcranial magnetic stimulation (TMS). Participants matched upright and inverted faces while TMS was delivered over each participant's functionally localized right occipital face area (rOFA) or right lateral occipital area (rLO). TMS delivered over rOFA disrupted the discrimination of upright and inverted faces while TMS delivered over rLO impaired inverted face discrimination only. These results provide causal evidence that upright faces are represented by face-specific mechanisms whereas inverted faces are represented by both face-specific and object-specific mechanisms. The similar sensitivity of the OFA to upright and inverted faces is consistent with the hypothesis that the OFA processes facial features at an early stage of face processing.     

A tale of two recognition systems: implications of the fusiform face area and the visual word form area for lateralized object recognition models

Two areas of current intense interest in the neuroimaging literature are that of the visual word form area (VWFA) and of the fusiform face area (FFA) and their roles in word and face perception, respectively. These two areas are of particular relevance to laterality research because visual word identification and face identification have long been shown to be especially lateralized to the left hemisphere and the right hemisphere, respectively. This review therefore seeks to evaluate their significance for the broader understanding of lateralization of object recognition. A multi-level model of lateralized object recognition is proposed based on a combination of behavioral and neuroimaging findings. Rather than seek to characterize hemispheric asymmetries according to a single principle (e.g., serial-parallel), it is suggested that current observations can be understood in terms of three asymmetric levels of processing, using the framework of the Janus model of hemispheric function. It is suggested that the left hemisphere represents features using an abstract-category code whereas the RH utilizes a specific-exemplar code. The relationships between these features are also coded asymmetrically, with the LH relying on associative co-occurrence values and the RH relying on spatial metrics. Finally, the LH controlled selection system focuses on isolating features and the RH focuses on conjoining features. It is suggested that each hemisphere utilizes efficient (apparently parallel) processing when stimuli are congruent with its preferred processing style and inefficient (apparently serial) processing when they are not, resulting in the typical left-lateralization for orthographic analysis and right-lateralization for face analysis.     

“A room full of strangers every day”: The psychosocial impact of developmental prosopagnosia on children and their families

Objective

Individuals with developmental prosopagnosia (‘face blindness’) have severe face recognition difficulties due to a failure to develop the necessary visual mechanisms for recognizing faces. These difficulties occur in the absence of brain damage and despite normal low-level vision and intellect. Adults with developmental prosopagnosia report serious personal and emotional consequences from their inability to recognize faces, but little is known about the psychosocial consequences in childhood. Given the importance of face recognition in daily life, and the potential for unique social consequences of impaired face recognition in childhood, we sought to evaluate the impact of developmental prosopagnosia on children and their families.

Methods

We conducted semi-structured interviews with 8 children with developmental prosopagnosia and their parents. A battery of face recognition tests was used to confirm the face recognition impairment reported by the parents of each child. We used thematic analysis to develop common themes among the psychosocial experiences of the children and their parents.

Results

Three themes were developed from the child reports: 1) awareness of their difficulties, 2) coping strategies, such as using non-facial cues to identify others, and 3) social implications, such as discomfort in, and avoidance of, social situations. These themes were paralleled by the parent reports and highlight the unique social and practical challenges associated with childhood developmental prosopagnosia.

Conclusion

Our findings indicate a need for increased awareness and treatment of developmental prosopagnosia to help these children manage their face recognition difficulties and to promote their social and emotional wellbeing.     

What the study of voice recognition in normal subjects and brain-damaged patients tells us about models of familiar people recognition

In recent years it has been shown that a disorder in recognizing familiar people can be observed in patients with lesions affecting the anterior parts of the temporal lobes and that these disorders can be multi-modal, simultaneously affecting the visual, auditory and linguistic channels that allow person identification. Several authors have also shown that patients with right anterior temporal atrophy are more impaired in assessing familiarity and in retrieving person-specific semantic information from faces than from names, whereas the opposite pattern of performance can be observed in patients with left temporal lobe atrophy. Voice recognition disorders have been studied much less even despite their clinical and theoretical importance. The aim of the present review, therefore, was to compare recognition of familiar faces and voices, taking into account not only results obtained in individual patients with right anterior temporal lesions, but also those of group studies of unselected right- and left brain-damaged patients and results of experimental investigations conducted on face and voice recognition in normal subjects. Results of the review showed that: (1) voice recognition disorders are mainly due to right temporal lesions, similarly to face recognition disorders; (2) famous voice recognition disorders can be dissociated from unfamiliar voice discrimination impairments; (3) although face and voice recognition disorders tend to co-occur, they can also dissociate and in these patients there is a prevalent involvement of the right fusiform gyrus when face recognition disorders are on the foreground, and of the right superior temporal gyrus when voice recognition disorders are prominent; (4) normal subjects have greater difficulty evaluating familiarity and drawing semantic information from the voices than from the faces of celebrities. These data are at variance with models which assume that familiarity feelings may be generated at the level of person identity nodes (PINs) and that the latter may be considered as modality-free gateways to single semantic systems in which information about people is stored in an amodal format.     

How Berlusconi keeps his face: a neuropsychological study in a case of semantic dementia

A patient (V.Z.) is described as being affected by progressive bilateral atrophy of the mesial temporal lobes resulting in semantic dementia. Vis-a-vis virtually nil recognition of even the most familiar faces (including those of her closest relatives) as well as of objects and animals, V.Z. could nevertheless consistently recognize and name the face of Silvio Berlusconi, the mass media tycoon and current Italian Prime Minister. The experimental investigation led to the conclusion that Mr Berlusconi's face was seen as an icon rather than as a face. This telling effect of Mr Berlusconi's pervasive propaganda constitutes an unprecedented case in the neuropsychological literature.     

The role of the eyes in processing an intact face and its scrambled image: A dense array ERP and low-resolution electromagnetic tomography (sLORETA) study

The aim of the present study was to test whether the eyes of an intact face produced a specific brain response compared to the mouth, nose, or hair and whether their specificity was also maintained in a scrambled face. Fifteen subjects were asked to focus visual attention on global and single elements in intact faces and in their scrambled image. EEG data were recorded from 256-Hydrocel Geodesic Sensor-Net200. Event-related potentials (ERPs) analyses showed a difference between the intact face and the scrambled face from N170 component until 600 ms on the occipito-temporal montage and at 400–600 ms on the frontal montage. Only the eyes showed a difference between conditions (intact/scrambled face) at 500 ms. The most activated source detected by sLORETA was the right middle temporal gyrus (BA21) for both conditions and for all elements. Left BA21 resulted in significantly more activation in response to eyes in the intact face compared to the eyes in the scrambled face at 500 ms. The left BA21 has a central role in high-level visual processing and in understanding others' intentions. These findings suggest a specificity of the eyes and indicate that the eyes play the social and communicative role of comprehending the nonverbal intentions of others only when inserted in an intact face.     

Reprint of: The amygdala and FFA track both social and non-social face dimensions

The amygdala is thought to perform a number of social functions, and has received much attention for its role in processing social properties of faces. In particular, it has been shown to respond more to facial expressions than to neutral faces, and more to positively valenced and negatively valenced faces than faces in the middle of the continuum. However, when these findings are viewed in the context of a multidimensional face space, an important question emerges. Face space is a vector space where every face can be represented as a point in the space. The origin of the space represents the average face. In this context, positively valenced and negatively valenced faces are further away from the average face than faces in the middle of the continuum. It is therefore unclear if the amygdala response to positively valenced and negatively valenced faces is due to their social properties or to their general distance from the average face. Here, we compared the amygdala response to a set of faces that varied along two dimensions centered around the average face but differing in social content. In both the amygdala and much of the posterior face network, we observed a similar response to both dimensions, with stronger responses to the extremes of the dimensions than to faces near the average face. These findings suggest that the responses in these regions to socially relevant faces may be partially due to general distance from the average face.