The existence of facial aftereffects suggests that shape-selective mechanisms at the higher stages of visual object coding -- similarly to the early processing of low-level visual features -- are adaptively recalibrated. Our goal was to uncover the ERP correlates of shape-selective adaptation and to test whether it is also involved in the visual processing of human body parts. We found that prolonged adaptation to female hands -- similarly to adaptation to female faces -- biased the judgements about the subsequently presented hand test stimuli: they were perceived more masculine than in the control conditions. We also showed that these hand aftereffects are size and orientation invariant. However, no aftereffects were found when the adaptor and test stimuli belonged to different categories (i.e. face adaptor and hand test, or vice versa), suggesting that the underlying adaptation mechanisms are category-specific. In accordance with the behavioral results, both adaptation to faces and hands resulted in a strong and category-specific modulation -- reduced amplitude and increased latency -- of the N170 component of ERP responses. Our findings suggest that shape-selective adaptation is a general mechanism of visual object processing and its neural effects are primarily reflected in the N170 component of the ERP responses.

Adaptation processes in human early visual cortical areas are sensitive to the exposure time of the adaptor stimulus. Here we investigated the effect of adaptation duration at the higher, shape-specific stages of visual processing using facial adaptation. It was found that long-term (5s) adaptation evokes facial aftereffects consisting of a position invariant as well as a position-specific component. As a result of adaptation to a female face, test faces were judged more masculine when they were displayed in the same location as the female adaptor face, as compared to that when they were presented in the opposite visual hemifield. However, aftereffects evoked by short-term (500 ms) adaptation were found to be entirely position invariant. In accordance with these behavioral results, we found that the adaptation effects, measured on the amplitude of the N170 ERP component consisted of a position-specific component only after long-term, but not after short-term adaptation conditions. These results suggest that both short and long exposure to a face stimulus leads to adaptation of position invariant face-selective processes, whereas adaptation of position-specific neural mechanisms of face processing requires long-term adaptation. Our findings imply that manipulating adaptation duration provides an opportunity to specifically adapt different neural processes of shape-specific coding and to investigate their stimulus selectivity.

We investigated the representation of objects' position at the higher, shape-selective stages of visual processing by testing the position-specificity of the behavioural and neural effects of facial adaptation. Here, we show that facial after-effects evoked by adaptation to both upright and upside-down faces are significantly larger when the adaptor and test faces are presented on the same retinal position than when they are displayed in different hemifields. Our event-related potential recordings revealed that adaptation effects measured on the amplitude of the N170 event-related potential component over the hemisphere that was contralateral to the test face stimulus also show strong position-specificity. These findings suggest that face adaptation effects are only partially translation invariant and facial after-effects measured with peripheral test stimuli primarily reflect the adaptation processes in the contralateral hemisphere.

No abstract

It has been shown that prolonged exposure to a human face leads to shape-selective visual aftereffects. It seems that these face-specific aftereffects (FAEs) have multiple components, related to the adaptation of earlier and higher level processing of visual stimuli. The largest magnitude of FAE, using long-term adaptation periods, is usually observed at the retinotopic position of the preceding adaptor stimulus. However, FAE is also detected, to a smaller degree, at other retinal positions in a spatially invariant way and this component depends less on the adaptation duration. Several lines of evidences suggest that while the position-specific FAE involves lower level areas of the ventral processing stream, the position-invariant FAE depends on the activation of higher level face-processing areas and the fusiform gyrus in particular. In the present paper, we summarize the available behavioural, electrophysiological and neuroimaging results regarding the spatial selectivity of FAE and discuss their implications for the visual stability of object representations across saccadic eye movements.

When observers are exposed to a distorted face the perceived configuration of a subsequently presented face is altered, a phenomenon called face distortion after-effect (FDAE). We compared the face-related components of the event-related potential (ERP) after adaptation to noise images--veridical and distorted faces. We found large bilateral adaptation effects on the P100 and N170 components that are related to face detection. Moreover, we found smaller adaptation effects on the N170, recorded over the right hemisphere, which can be related to the behavioural distortion after-effect and to face configurations. Our results suggest that the observed ERP adaptation effects are general for various steps of face processing and that the FDAEs similarly to gender after-effects are related to the early face-specific ERP components.

Congenital prosopagnosia is lifelong face-recognition impairment in the absence of evidence for structural brain damage. To study the neural correlates of congenital prosopagnosia, we measured the face-sensitive N170 component of the event-related potential in three members of the same family (father (56 y), son (25 y) and daughter (22 y)) and in age-matched neurotypical participants (young controls: n = 14; 24.5 y±2.1; old controls: n = 6; 57.3 y±5.4). To compare the face sensitivity of N170 in congenital prosopagnosic and neurotypical participants we measured the event-related potentials for faces and phase-scrambled random noise stimuli. In neurotypicals we found significantly larger N170 amplitude for faces compared to noise stimuli, reflecting normal early face processing. The congenital prosopagnosic participants, by contrast, showed reduced face sensitivity of the N170, and this was due to a larger than normal noise-elicited N170, rather than to a smaller face-elicited N170. Interestingly, single-trial analysis revealed that the lack of face sensitivity in congenital prosopagnosia is related to a larger oscillatory power and phase-locking in the theta frequency-band (4–7 Hz, 130–190 ms) as well as to a lower intertrial jitter of the response latency for the noise stimuli. Altogether, these results suggest that congenital prosopagnosia is due to the deficit of early, structural encoding steps of face perception in filtering between face and non-face stimuli.

Previous studies have found that the amplitude of the early event-related potential (ERP) components evoked by faces, such as N170 and P2, changes systematically as a function of noise added to the stimuli. This change has been linked to an increased perceptual processing demand and to enhanced difficulty in perceptual decision making about faces. However, to date it has not yet been tested whether noise manipulation affects the neural correlates of decisions about face and non-face stimuli similarly. To this end, we measured the ERPs for faces and cars at three different phase noise levels. Subjects performed the same two-alternative age-discrimination task on stimuli chosen from young–old morphing continua that were created from faces as well as cars and were calibrated to lead to similar performances at each noise-level. Adding phase noise to the stimuli reduced performance and enhanced response latency for the two categories to the same extent. Parallel to that, phase noise reduced the amplitude and prolonged the latency of the face-specific N170 component. The amplitude of the P1 showed category-specific noise dependence: it was enhanced over the right hemisphere for cars and over the left hemisphere for faces as a result of adding phase noise to the stimuli, but remained stable across noise levels for cars over the left and for faces over the right hemisphere. Moreover, noise modulation altered the category-selectivity of the N170, while the P2 ERP component, typically associated with task decision difficulty, was larger for the more noisy stimuli regardless of stimulus category. Our results suggest that the category-specificity of noise-induced modulations of ERP responses starts at around 100 ms post-stimulus.