The animal brain is endowed with an innate sense of number allowing to intuitively perceive the approximate quantity of items in a scene, or “numerosity.” This ability is not limited to items distributed in space, but also to events unfolding in time and to the average numerosity of dynamic scenes. How the brain computes and represents the average numerosity over time, however, remains unclear. Here, we investigate the mechanisms and EEG signature of the perception of average numerosity over time. To do so, we used stimuli composed of a variable number (3–12) of briefly presented dot arrays (50 msec each) and asked participants to judge the average numerosity of the sequence. We first show that the weight of different portions of the stimuli in determining the judgment depends on how many arrays are included in the sequence itself: the longer the sequence, the lower the weight of the latest arrays. Second, we show systematic adaptation effects across stimuli in consecutive trials. Importantly, the EEG results highlight two processing stages whereby the amplitude of occipital ERPs reflects the adaptation effect (∼300 msec after stimulus onset) and the accuracy and precision of average numerosity judgments (∼450–700 msec). These two stages are consistent with processes involved with the representation of perceived average numerosity and with perceptual decision-making, respectively. Overall, our findings provide new evidence showing how the visual system computes the average numerosity of dynamic visual stimuli, and support the existence of a dedicated, relatively low-level perceptual mechanism mediating this process.

The recent upsurge of interest in brain mechanisms of time perception is beginning to converge on some new starting points for investigating this long under studied aspect of our experience. In four experiments, we asked whether disruption of normal activity in human MT/V5 would interfere with temporal discrimination. Although clearly associated with both spatial and motion processing, MT/V5 has not yet been implicated in temporal processes. Following predictions from brain imaging studies that have shown the parietal cortex to be important in human time perception, we also asked whether disruption of either the left or right parietal cortex would interfere with time perception preferentially in the auditory or visual domain. The results show that the right posterior parietal cortex is important for timing of auditory and visual stimuli and that MT/V5 is necessary for timing only of visual events.

In everyday life, temporal information is used for both perception and action, but whether these two functions reflect the operation of similar or different neural circuits is unclear. We used functional magnetic resonance imaging to investigate the neural correlates of processing temporal information when either a motor or a perceptual representation is used. Participants viewed two identical sequences of visual stimuli and used the information differently to perform either a temporal reproduction or a temporal estimation task. By comparing brain activity evoked by these tasks and control conditions, we explored commonalities and differences in brain areas involved in reproduction and estimation of temporal intervals. The basal ganglia and the cerebellum were commonly active in both temporal tasks, consistent with suggestions that perception and production of time are subserved by the same mechanisms. However, only in the reproduction task was activity observed in a wider cortical network including the right pre-SMA, left middle frontal gyrus, left premotor cortex, with a more reliable activity in the right inferior parietal cortex, left fusiform gyrus, and the right extrastriate visual area V5/MT. Our findings point to a role for the parietal cortex as an interface between sensory and motor processes and suggest that it may be a key node in translation of temporal information into action. Furthermore, we discuss the potential importance of the extrastriate cortex in processing visual time in the context of recent findings.