Single-unit recordings in macaque monkeys have identified effector-specific regions in posterior parietal cortex (PPC), but functional neuroimaging in the human has yielded controversial results. Here we used on-line repetitive transcranial magnetic stimulation (rTMS) to determine saccade and reach specificity in human PPC. A short train of three TMS pulses (separated by an interval of 100 ms) was delivered to superior parieto-occipital cortex (SPOC), a region over the midposterior intraparietal sulcus (mIPS), and a site close to caudal IPS situated over the angular gyrus (AG) during a brief memory interval while subjects planned either a saccade or reach with the left or right hand. Behavioral measures then were compared to controls without rTMS. Stimulation of mIPS and AG produced similar patterns: increased end-point variability for reaches and decreased saccade accuracy for contralateral targets. In contrast, stimulation of SPOC deviated reach end points toward visual fixation and had no effect on saccades. Contralateral-limb specificity was highest for AG and lowest for SPOC. Visual feedback of the hand negated rTMS-induced disruptions of the reach plan for mIPS and AG, but not SPOC. These results suggest that human SPOC is specialized for encoding retinally peripheral reach goals, whereas more anterior-lateral regions (mIPS and AG) along the IPS possess overlapping maps for saccade and reach planning and are more closely involved in motor details (i.e., planning the reach vector for a specific hand). This work provides the first causal evidence for functional specificity of these parietal regions in healthy humans.

Summary We have employed molecular probes produced from DNA fragments of human papillomavirus, cloned into prokaryotic vectors, to detect virus nucleic acid sequences in extracts of human oral tissues. The study was conducted with duplicate coded snap-frozen tissue biopsies from which frozen sections had been taken to accurately assess the pathology of each particular sample.The results show that a large proportion of the oral biopsies contained DNA which hybridized to the viral DNA probes, even under conditions of high stringency. The presence of virus did not correlate with neoplasia in the tissues examined, but HPV like sequences were found in a high proportion (80%) of biopsies taken from areas of keratosis and lichen planus and also in 41 to 46% of normal and tumour tissues.

The posterior parietal cortex (PPC) plays a role in spatial updating of goals for eye and arm movements across saccades, but less is known about its role in updating perceptual memory. We reported previously that transsaccadic memory has a capacity for storing the orientations of three to four Gabor patches either within a single fixation (fixation task) or between separate fixations (saccade task). Here, we tested the role of the PPC in transsaccadic memory in eight subjects by simultaneously applying single-pulse transcranial magnetic stimulation (TMS) over the right and left PPC, over several control sites, and comparing these to behavioral controls with no TMS. In TMS trials, we randomly delivered pulses at one of three different time intervals around the time of the saccade, or at an equivalent time in the fixation task. Controls confirmed that subjects could normally retain at least three visual features. TMS over the left PPC and a control site had no significant effect on this performance. However, TMS over the right PPC disrupted memory performance in both tasks. This TMS-induced effect was most disruptive in the saccade task, in particular when stimulation coincided more closely with saccade timing. Here, the capacity to compare presaccadic and postsaccadic features was reduced to one object, as expected if the spatial aspect of memory was disrupted. This finding suggests that right PPC plays a role in the spatial processing involved in transsaccadic memory of visual features. We propose that this process uses saccade-related feedback signals similar to those observed in spatial updating.

How we perceive the visual world as stable and unified suggests the existence of transsaccadic integration that retains and integrates visual information from one eye fixation to another eye fixation across saccadic eye movements. However, the capacity of transsaccadic integration is still a subject of controversy. We tested our subjects' memory capacity of two basic visual features, i.e. luminance (Experiment 1) and orientation (Experiment 2), both within a single fixation (i.e. visual working memory) and between separate fixations (i.e. transsaccadic memory). Experiment 2 was repeated, but attention allocation was manipulated using attentional cues at either the target or distracter (Experiment 3). Subjects were able to retain 3-4 objects in transsaccadic memory for luminance and orientation; errors generally increased as saccade size increased; and, subjects were more accurate when attention was allocated to the same location as the impending target. These results were modelled by inputting a noisy extra-retinal signal into an eye-centered feature map. Our results suggest that transsaccadic memory has a similar capacity for storing simple visual features as basic visual memory, but this capacity is dependent both on the metrics of the saccade and allocation of attention.

Transsaccadic integration (TSI) refers to the perceptual integration of visual information collected across separate gaze fixations. Current theories of TSI disagree on whether it relies solely on visual algorithms or also uses extra-retinal signals. We designed a task in which subjects had to rely on internal oculomotor signals to synthesize remembered stimulus features presented within separate fixations. Using a mouse-controlled pointer, subjects estimated the intersection point of two successively presented bars, in the dark, under two conditions: Saccade task (bars viewed in separate fixations) and Fixation task (bars viewed in one fixation). Small, but systematic biases were observed in both intersection tasks, including position-dependent vertical undershoots and order-dependent horizontal biases. However, the magnitude of these errors was statistically indistinguishable in the Saccade and Fixation tasks. Moreover, part of the errors in the Saccade task were dependent on saccade metrics, showing that egocentric oculomotor signals were used to fuse remembered location and orientation features across saccades. We hypothesize that these extra-retinal signals are normally used to reduce the computational load of calculating visual correspondence between fixations. We further hypothesize that TSI may be implemented within dynamically updated recurrent feedback loops that interconnect a common eye-centered map in occipital cortex with both the "dorsal" and "ventral" streams of visual analysis.

Constructing an internal representation of the world from successive visual fixations, i.e. separated by saccadic eye movements, is known as trans-saccadic perception. Research on trans-saccadic perception (TSP) has been traditionally aimed at resolving the problems of memory capacity and visual integration across saccades. In this paper, we review this literature on TSP with a focus on research showing that egocentric measures of the saccadic eye movement can be used to integrate simple object features across saccades, and that the memory capacity for items retained across saccades, like visual working memory, is restricted to about three to four items. We also review recent transcranial magnetic stimulation experiments which suggest that the right parietal eye field and frontal eye fields play a key functional role in spatial updating of objects in TSP. We conclude by speculating on possible cortical mechanisms for governing egocentric spatial updating of multiple objects in TSP.

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