Timing and tuning for familiarity of cortical responses to faces.

Different kinds of known faces activate brain areas to dissimilar degrees. However, the tuning to type of knowledge, and the temporal course of activation, of each area have not been well characterized. Here we measured, with functional magnetic resonance imaging, brain activity elicited by unfamiliar, visually familiar, and personally-familiar faces. We assessed response amplitude and duration using flexible hemodynamic response functions, as well as the tuning to face type, of regions within the face processing system. Core face processing areas (occipital and fusiform face areas) responded to all types of faces with only small differences in amplitude and duration. In contrast, most areas of the extended face processing system (medial orbito-frontal, anterior and posterior cingulate) had weak responses to unfamiliar and visually-familiar faces, but were highly tuned and exhibited prolonged responses to personally-familiar faces. This indicates that the neural processing of different types of familiar faces not only differs in degree, but is probably mediated by qualitatively distinct mechanisms.

Covert face recognition without the fusiform-temporal pathways.

Patients with prosopagnosia are unable to recognize faces consciously, but when tested indirectly they can reveal residual identification abilities. The neural circuitry underlying this covert recognition is still unknown. One candidate for this function is the partial survival of a pathway linking the fusiform face area (FFA) and anterior-inferior temporal (AIT) cortex, which has been shown to be essential for conscious face identification. Here we performed functional magnetic, and diffusion tensor imaging in FE, a patient with severe prosopagnosia, with the goal of identifying the neural substrates of his robust covert face recognition. FE presented massive bilateral lesions in the fusiform gyri that eliminated both FFAs, and also disrupted the fibers within the inferior longitudinal fasciculi that link the visual areas with the AITs and medial temporal lobes. Therefore participation of the fusiform-temporal pathway in his covert recognition was precluded. However, face-selective activations were found bilaterally in his occipital gyri and in his extended face system (posterior cingulate and orbitofrontal areas), the latter with larger responses for previously-known faces than for faces of strangers. In the right hemisphere, these surviving face selective-areas were connected via a partially persevered inferior fronto-occipital fasciculus. This suggests an alternative occipito-frontal pathway, absent from current models of face processing, that could explain the patient's covert recognition while also playing a role in unconscious processing during normal cognition.

Hemispheric modulations of alpha-band power reflect the rightward shift in attention induced by enhanced attentional load.

Rightward shifts in attention are a common consequence of brain injury. A growing body of evidence appears to suggest that increases in attentional load, and decreases in alertness can lead to rightward shifts in attention in healthy and patient populations. It is unclear however whether these factors affect spatial biases in attention at the level of preparatory control processes or at the level of stimulus driven expression mechanisms. Whilst such effects cannot easily be dissociated behaviourally, the robust association between changes in alpha-band activity and shifts in visual attention provides a neural marker by which the temporal dynamics of effects of attentional load on spatial processing might be examined. Here we use electroencephalography to examine the relationship between modulations in alpha-band activity and behavioural outcome on a dual task paradigm comprising a detection task (t1), closely followed by a temporal order judgment task (t2). We examine the effects of high (respond to t1 and t2) and low (t2 only) attentional load conditions on spatial bias and changes in lateralization of alpha-band activity over the course of the trial. As anticipated a rightward bias in detecting target onsets was observed in the temporal order judgment task (t2) under conditions of high attentional load. This rightward shift in attention was associated with changes in the lateralization of alpha-band activity that occurred only after the presentation of t2, suggesting that attentional load may primarily influence expression mechanisms.

Right impairment of temporal order judgements in dyslexic children.

This study investigates the spatial bias of visual attention measured by a temporal order judgement (TOJ) task and the influence of a high attentional load condition in a group of dyslexic children compared to a control group with normal reading skills (each group N=10). The TOJ task (T2) was placed after a shape discrimination task (T1). In a low attentional load block participants worked only on T2, whereas in the high attentional load block they were required to process both T1 and T2. Several t-tests were executed to compare performance between conditions and groups. In the low attentional load conditions, results in dyslexic children were significantly impaired for the right visual field compared to a control group. The high attentional load conditions did not enhance these effects and seems to provoke the same leftward bias in the control group.