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Until recently, most of the studies on face perception were conducted using still stimuli, such as drawings or photographs. However, the faces that we encounter in everyday life are constantly in motion and are very rarely static. It has been shown that besides facilitating communication, such facial movements can also convey information about emotions, age, gender, and to a certain extent about the identity of the individual.

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The question is then to know how exactly movement help in identifying a face. Is it because we have a better structural representation of the faces in motion, or is it because our facial representations contain a specific dynamic signature? Can we recognise faces by the way they move? How do the cues about shape and facial movements interact with each other? The research project proposed here will study the role of facial movements in the processing of faces such as the recognition of facial identity and the recognition of facial emotions.

It has been shown in the literature that although the information obtained from faces in movement can facilitate the recognition of familiar faces (Lander and Bruce, 2000; Lander et al., 1999), its effects on unfamiliar faces are far from being certain (Christie and Bruce, 1998; Pike et al., 1997). It has been suggested that either movement does not facilitate the recognition of unfamiliar faces, or its benefits are counterbalanced by other factors. One of these factors could be that the social importance of facial movements could distract the participants, preventing them from encoding the identity of the presented faces.

Recently, using studies on the activation of cortical areas in response to faces stimuli, Haxby and collaborators have proposed a distributed neural system for face perception in which invariant representations and changing aspects of faces are differentiated (Haxby et al., 2000). Haxby et al. propose the involvement of two main cortical areas to illustrate their model. The first region is the lateral fusiform gyrus (‘Fusiform Face Area’, FFA), which has been revealed in many neuro-imaging studies on face perception, and represents the invariant facial information useful to identify faces.

The second region is the posterior Superior Temporal Sulcus (pSTS), which is involved in the processing of the changing aspects of the movement of faces. Neurophysiological studies in non human primates and neuro-imaging studies in humans have demonstrated that this cortical area is involved in the detection of information on gaze, the orientation of the head, and on expression (Allison et al., 2000; Haxby et al., 2000; Haxby et al., 2002; Narumoto et al., 2001).

It has also been shown that the STS could be involved in the perception of biological movements of the body, hands, eyes, and mouth (Allison et al., 2000). Moreover, the STS system is extended to cortical areas that are involved in the detection of gaze and orientation, in the perception of speech through the movements of the mouth, and in the perception of emotions. The infero-temporal system is extended to cortical areas involved in the retrieval of the identity of individuals, their names, and of biographical information (Haxby et al., 2000).

The functional division between these high-level cortical areas for the processing of dynamic and invariant information about faces is in agreement with the transfer of visual information, from the retina to the ventral stream on one hand (high resolution and colour sensitivity, object recognition) and to the dorsal stream on the other hand (low resolution and movement sensitivity, spatial orientation) – (Ungerleider and Mishkin, 1982). Therefore, the dynamic information about faces could mainly be processed by the dorsal stream, while the static characteristics about faces would mainly be processed by the ventral stream (Haxby et al., 2000).




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