Yes / The goal of this study was to investigate the reference frames used in perceptual encoding and storage of visual motion information. In our experiments, observers viewed multiple moving objects and reported the direction of motion of a randomly selected item. Using a vector-decomposition technique, we computed performance during smooth pursuit with respect to a spatiotopic (nonretinotopic) and to a retinotopic component and compared them with performance during fixation, which served as the baseline. For the stimulus encoding stage, which precedes memory, we found that the reference frame depends on the stimulus set size. For a single moving target, the spatiotopic reference frame had the most significant contribution with some additional contribution from the retinotopic reference frame. When the number of items increased (Set Sizes 3 to 7), the spatiotopic reference frame was able to account for the performance. Finally, when the number of items became larger than 7, the distinction between reference frames vanished. We interpret this finding as a switch to a more abstract nonmetric encoding of motion direction. We found that the retinotopic reference frame was not used in memory. Taken together with other studies, our results suggest that, whereas a retinotopic reference frame may be employed for controlling eye movements, perception and memory use primarily nonretinotopic reference frames. Furthermore, the use of nonretinotopic reference frames appears to be capacity limited. In the case of complex stimuli, the visual system may use perceptual grouping in order to simplify the complexity of stimuli or resort to a nonmetric abstract coding of motion information.

Yes / The Atkinson-Shiffrin modal model forms the foundation of our understanding of human memory. It consists of three stores (Sensory Memory (SM), also called iconic memory, Short-Term Memory (STM), and Long-Term Memory (LTM)), each tuned to a different time-scale. Since its inception, the STM and LTM components of the modal model have undergone significant modifications, while SM has remained largely unchanged, representing a large capacity system funneling information into STM. In the laboratory, visual memory is usually tested by presenting a brief static stimulus and, after a delay, asking observers to report some aspect of the stimulus. However, under ecological viewing conditions, our visual system receives a continuous stream of inputs, which is segmented into distinct spatio-temporal segments, called events. Events are further segmented into event-segments. Here we show that SM is not an unspecific general funnel to STM but is allocated exclusively to the current event-segment. We used a Multiple-Object Tracking (MOT) paradigm in which observers were presented with disks moving in different directions, along bi-linear trajectories, i.e., linear trajectories, with a single deviation in direction at the mid-point of each trajectory. The synchronized deviation of all of the trajectories produced an event stimulus consisting of two event-segments. Observers reported the pre-deviation or the post-deviation directions of the trajectories. By analyzing observers' responses in partial- and full-report conditions, we investigated the involvement of SM for the two event-segments. The hallmarks of SM hold only for the current event segment. As the large capacity SM stores only items involved in the current event-segment, the need for event-tagging in SM is eliminated, speeding up processing in active vision. By characterizing how memory systems are interfaced with ecological events, this new model extends the Atkinson-Shiffrin model by specifying how events are stored in the first stage of multi-store memory systems.

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