Saccadic selection in visual working memory is robust across the visual field and linked to saccade metrics: Evidence from nine experiments and more than 100,000 trials.

Visual working memory and actions are closely intertwined. Memory can guide our actions, but actions also impact what we remember. Even during memory maintenance, actions such as saccadic eye movements select content in visual working memory, resulting in better memory at locations that are congruent with the action goal as compared to incongruent locations. Here, we further substantiate the claim that saccadic eye movements are fundamentally linked to visual working memory by analyzing a large data set (> 100k trials) of nine experiments (eight of them previously published). Using Bayesian hierarchical models, we demonstrate robust saccadic selection across the full range of probed saccade directions, manifesting as better memory performance at the saccade goal irrespective of its location in the visual field. By inspecting individual differences in saccadic selection, we show that saccadic selection was highly prevalent in the population. Moreover, both saccade metrics and visual working memory performance varied considerably across the visual field. Crucially, however, both idiosyncratic and systematic visual field anisotropies were not correlated between visual working memory and the oculomotor system, suggesting that they resulted from different sources (e.g., rely on separate spatial maps). In stark contrast, trial-by-trial variations in saccade metrics were strongly associated with memory performance: At any given location, shorter saccade latencies and more accurate saccades were associated with better memory performance, undergirding a robust link between action selection and visual memory. (PsycInfo Database Record (c) 2024 APA, all rights reserved).

Foveal vision anticipates defining features of eye movement targets.

High-acuity foveal processing is vital for human vision. Nonetheless, little is known about how the preparation of large-scale rapid eye movements (saccades) affects visual sensitivity in the center of gaze. Based on findings from passive fixation tasks, we hypothesized that during saccade preparation, foveal processing anticipates soon-to-be fixated visual features. Using a dynamic large-field noise paradigm, we indeed demonstrate that defining features of an eye movement target are enhanced in the pre-saccadic center of gaze. Enhancement manifested as higher Hit Rates for foveal probes with target-congruent orientation and a sensitization to incidental, target-like orientation information in foveally presented noise. Enhancement was spatially confined to the center of gaze and its immediate vicinity, even after parafoveal task performance had been raised to a foveal level. Moreover, foveal enhancement during saccade preparation was more pronounced and developed faster than enhancement during passive fixation. Based on these findings, we suggest a crucial contribution of foveal processing to trans-saccadic visual continuity: Foveal processing of saccade targets commences before the movement is executed and thereby enables a seamless transition once the center of gaze reaches the target.

Transsaccadic integration relies on a limited memory resource.

Saccadic eye movements cause large-scale transformations of the image falling on the retina. Rather than starting visual processing anew after each saccade, the visual system combines post-saccadic information with visual input from before the saccade. Crucially, the relative contribution of each source of information is weighted according to its precision, consistent with principles of optimal integration. We reasoned that, if pre-saccadic input is maintained in a resource-limited store, such as visual working memory, its precision will depend on the number of items stored, as well as their attentional priority. Observers estimated the color of stimuli that changed imperceptibly during a saccade, and we examined where reports fell on the continuum between pre- and post-saccadic values. Bias toward the post-saccadic color increased with the set size of the pre-saccadic display, consistent with an increased weighting of the post-saccadic input as precision of the pre-saccadic representation declined. In a second experiment, we investigated if transsaccadic memory resources are preferentially allocated to attentionally prioritized items. An arrow cue indicated one pre-saccadic item as more likely to be chosen for report. As predicted, valid cues increased response precision and biased responses toward the pre-saccadic color. We conclude that transsaccadic integration relies on a limited memory resource that is flexibly distributed between pre-saccadic stimuli.

The peripheral sensitivity profile at the saccade target reshapes during saccade preparation.

Goal-directed eye movements (saccades) bring peripheral objects of interest into high-acuity foveal vision. In preparation for the incoming foveal image, the perception of the saccade target may sharpen gradually before the eye movement is executed. Indeed, previous studies suggest that pre-saccadic attention shifts enhance sensitivity to high spatial frequencies (SFs) more than sensitivity to lower SFs. This pattern, however, was observed within a narrow frequency range and may reflect local changes in the shape of a broader underlying sensitivity profile. Depending on the development of the profile's shape, SFs above the previously examined range may profit less from saccade preparation. To assess the impact of saccade preparation on the shape of a broader sensitivity profile, we prompted observers to discriminate the orientation of a sinusoidal grating (the probe) presented briefly at the target of an impending saccade, at 10 dva (degree of visual angle) eccentricity. The probe's SF ranged from 1 to 5.5 cycles per dva (cpd) and was unpredictable on a given trial. We fitted observers' response accuracies across SFs with a log-parabolic, that is, inverted U-shaped function. Long before saccade onset, the profile peaked at .6 cpd and dropped off towards lower and higher SFs with broad bandwidth. During saccade preparation, the peak of the profile increased and shifted towards higher SFs while the bandwidth of the profile decreased. As a consequence of this reshaping process, pre-saccadic enhancement increased with SF up to 2.5 cpd, corroborating previous findings. Sensitivities to higher SFs, however, profited less from saccade preparation. We conclude that the extent of pre-saccadic enhancement to a particular SF is governed by its position on a broader sensitivity profile which reshapes substantially during saccade preparation. The shift of the profile's peak towards higher SFs increases resolution at the saccade target even when the features of relevant visual information are unpredictable.