John Towler

The face-sensitive N170 component in developmental prosopagnosia.

Individuals with developmental prosopagnosia (DP) show severe face recognition deficits in the absence of any history of neurological damage. To examine the time-course of face processing in DP, we measured the face-sensitive N170 component of the event-related brain potential (ERP) in a group of 16 participants with DP and 16 age-matched control participants. Reliable enhancements of N170 amplitudes in response to upright faces relative to houses were found for the DP group. This effect was equivalent in size to the effect observed for controls, demonstrating normal face-sensitivity of the N170 component in DP. Face inversion enhanced N170 amplitudes in the control group, but not for DPs, suggesting that many DPs do not differentiate between upright and inverted faces in the typical manner. These N170 face inversion effects were present for younger but not older controls, while they were absent for both younger and older DPs. Results suggest that the early face-sensitivity of visual processing is preserved in most individuals with DP, but that the face processing system in many DPs is not selectively tuned to the canonical upright orientation of faces.

Response of face-selective brain regions to trustworthiness and gender of faces

Neuropsychological and neuroimaging studies have demonstrated a role for the amygdala in processing the perceived trustworthiness of faces, but it remains uncertain whether its responses are linear (with the greatest response to the least trustworthy-looking faces), or quadratic (with increased fMRI signal for the dimension extremes). It is also unclear whether the trustworthiness of the stimuli is crucial or if the same response pattern can be found for faces varying along other dimensions. In addition, the responses to perceived trustworthiness of face-selective regions other than the amygdala are seldom reported. The present study addressed these issues using a novel set of stimuli created through computer image-manipulation both to maximise the presence of naturally occurring cues that underpin trustworthiness judgments and to allow systematic manipulation of these cues. With a block-design fMRI paradigm, we investigated neural responses to computer-manipulated trustworthiness in the amygdala and core face-selective regions in the occipital and temporal lobes. We asked whether the activation pattern is specific for differences in trustworthiness or whether it would also track variation along an orthogonal male-female gender dimension. The main findings were quadratic responses to changes in both trustworthiness and gender in all regions. These results are consistent with the idea that face-responsive brain regions are sensitive to face distinctiveness as well as the social meaning of the face features.

Electrophysiological studies of face processing in developmental prosopagnosia: Neuropsychological and neurodevelopmental perspectives

People with developmental prosopagnosia (DP) show severe face-recognition deficits that typically emerge during childhood without history of neurological damage. We review findings from recent event-related brain potential (ERP) studies of face perception and face recognition in DP. The generic face-sensitivity of the N170 component is present in most DPs, suggesting rapid category-selective streaming of facial information. In contrast, DPs show atypical N170 face inversion effects, indicative of impaired structural encoding, specifically for upright faces. In line with neurodevelopmental accounts of DP, these effects are similar to those observed for other developmental disorders, as well as for younger children and older adults. Identity-sensitive ERP components (N250, P600f) triggered during successful face recognition are similar for DPs and control participants, indicating that the same mechanisms are active in both groups. The presence of covert face-recognition effects for the N250 component suggests that visual face memory and semantic memory can become disconnected in some individuals with DP. The implications of these results for neuropsychological and neurodevelopmental perspectives on DP are discussed.

The cognitive and neural basis of developmental prosopagnosia

Developmental prosopagnosia (DP) is a severe impairment of visual face recognition in the absence of any apparent brain damage. The factors responsible for DP have not yet been fully identified. This article provides a selective review of recent studies investigating cognitive and neural processes that may contribute to the face recognition deficits in DP, focusing primarily on event-related brain potential (ERP) measures of face perception and recognition. Studies that measured the face-sensitive N170 component as a marker of perceptual face processing have shown that the perceptual discrimination between faces and non-face objects is intact in DP. Other N170 studies suggest that faces are not represented in the typical fashion in DP. Individuals with DP appear to have specific difficulties in processing spatial and contrast deviations from canonical upright visual–perceptual face templates. The rapid detection of emotional facial expressions appears to be unaffected in DP. ERP studies of the activation of visual memory for individual faces and of the explicit identification of particular individuals have revealed differences between DPs and controls in the timing of these processes and in the links between visual face memory and explicit face recognition. These observations suggest that the speed and efficiency of information propagation through the cortical face network is altered in DP. The nature of the perceptual impairments in DP suggests that atypical visual experience with the eye region of faces over development may be an important contributing factor to DP.

The Focus of Spatial Attention Determines the Number and Precision of Face Representations in Working Memory

The capacity of visual working memory for faces is extremely limited, but the reasons for these limitations remain unknown. We employed event-related brain potential measures to demonstrate that individual faces have to be focally attended in order to be maintained in working memory, and that attention is allocated to only a single face at a time. When 2 faces have to be memorized simultaneously in a face identity-matching task, the focus of spatial attention during encoding predicts which of these faces can be successfully maintained in working memory and matched to a subsequent test face. We also show that memory representations of attended faces are maintained in a position-dependent fashion. These findings demonstrate that the limited capacity of face memory is directly linked to capacity limits of spatial attention during the encoding and maintenance of individual face representations. We suggest that the capacity and distribution of selective spatial attention is a dynamic resource that constrains the capacity and fidelity of working memory for faces.

Normal perception of Mooney faces in developmental prosopagnosia: Evidence from the N170 component and rapid neural adaptation

Individuals with developmental prosopagnosia (DP) have a severe difficulty recognizing the faces of known individuals in the absence of any history of neurological damage. These recognition problems may be linked to selective deficits in the holistic/configural processing of faces. We used two-tone Mooney images to study the processing of faces versus non-face objects in DP when it is based on holistic information (or the facial gestalt) in the absence of obvious local cues about facial features. A rapid adaptation procedure was employed for a group of 16 DPs. Naturalistic photographs of upright faces were preceded by upright or inverted Mooney faces or by Mooney houses. DPs showed face-sensitive N170 components in response to Mooney faces versus houses, and N170 amplitude reductions for inverted as compared to upright Mooney faces. They also showed the typical pattern of N170 adaptation effects, with reduced N170 components when upright naturalistic test faces were preceded by upright Mooney faces, demonstrating that the perception of Mooney and naturalistic faces recruits shared neural populations. Our findings demonstrate that individuals with DP can utilize global information about face configurations for categorical discriminations between faces and non-face objects, and suggest that face processing deficits emerge primarily at more fine-grained higher level stages of face perception.

Early stages of perceptual face processing are confined to the contralateral hemisphere: Evidence from the N170 component

High-level visual object processing is often assumed to be largely position-independent. Here we demonstrate that when faces and non-face objects simultaneously appear in opposite visual hemifields, the face-sensitive N170 component of the event-related brain potential (ERP) is exclusively generated in the contralateral hemisphere. The effects of face inversion on N170 amplitudes and latencies also show strong contralateral biases. These results reveal that retinotopic biases in low-level visual cortex extend well into category-selective high-level vision. We suggest that the contralateral organisation of face-sensitive visual processing results from generic competitive interactions between hemispheres during the simultaneous perception of visual objects.

Perceptual face processing in developmental prosopagnosia is not sensitive to the canonical location of face parts

Individuals with developmental prosopagnosia (DP) are strongly impaired in recognizing faces, but it is controversial whether this deficit is linked to atypical visual-perceptual face processing mechanisms. Previous behavioural studies have suggested that face perception in DP might be less sensitive to the canonical spatial configuration of face parts in upright faces. To test this prediction, we recorded event-related brain potentials (ERPs) to intact upright faces and to faces with spatially scrambled parts (eyes, nose, and mouth) in a group of ten participants with DP and a group of ten age-matched control participants with normal face recognition abilities. The face-sensitive N170 component and the vertex positive potential (VPP) were both enhanced and delayed for scrambled as compared to intact faces in the control group. In contrast, N170 and VPP amplitude enhancements to scrambled faces were absent in the DP group. For control participants, the N170 to scrambled faces was also sensitive to feature locations, with larger and delayed N170 components contralateral to the side where all features appeared in a non-canonical position. No such differences were present in the DP group. These findings suggest that spatial templates of the prototypical feature locations within an upright face are selectively impaired in DP.

Facial misidentifications arise from the erroneous activation of visual face memory

Misidentifications are a common phenomenon in unfamiliar face processing, but little is known about the underlying cognitive and neural mechanisms. We used the face identity-sensitive N250r component of the event-related brain potential as a measure of identity-sensitive face matching process in visual working memory. Two face images were presented in rapid succession, and participants had to judge whether they showed the same or two different individuals. Identity match and mismatch trials were presented in random sequence. On similar mismatch trials, perceptually similar faces of two different individuals were shown, while two physically distinct faces were presented on dissimilar mismatch trials. Misidentification errors occurred on 40% of all similar mismatch trials. N250r components were elicited not only in response to an identity match, but also on trials with misidentification errors. This misidentification N250r was smaller and emerged later than the N250r to correctly detected identity repetitions. Importantly, N250r components were entirely eliminated on similar mismatch trials where participants correctly reported two different facial identities. Results show that misidentification errors are not primarily a post-perceptual decision-related phenomenon, but are generated during early visual stages of identity-related face processing. Misidentification errors occur when stored representations of a particular individual face in visual working memory are incorrectly activated by a perceptual match with a different face.

Reduced sensitivity to contrast signals from the eye region in developmental prosopagnosia.

Contrast-related signals from the eye region are known to be important for the processing of facial identity. Individuals with developmental prosopagnosia (DP) have severe face recognition problems, which may be linked to deficits in the perceptual processing of identity-related information from the eyes. We tested this hypothesis by measuring N170 components in DP participants and age-matched controls in response to face images where the contrast polarity of the eyes and of other face parts was independently manipulated. In different trials, participants fixated either the eye region or the lower part of a face. In the Control group, contrast-reversal of the eyes resulted in enhanced and delayed N170 components, irrespective of the contrast of other face parts and of gaze location. In the DP group, these effects of eye contrast on N170 amplitudes were strongly and significantly reduced, demonstrating that perceptual face processing in DP is less well tuned to contrast information from the eye region. Inverting the contrast of other parts of the face affected N170 amplitudes only when fixation was outside the eye region. This effect did not differ between the two groups, indicating that DPs are not generally insensitive to the contrast polarity of face images. These results provide new evidence that a selective deficit in detecting and analysing identity-related information provided by contrast signals from the eye region may contribute to the face recognition impairment in DP.