Fast and nonuniform dynamics of perisaccadic vision in the central fovea.

Humans use rapid eye movements (saccades) to inspect stimuli with the foveola, the region of the retina where receptors are most densely packed. It is well established that visual sensitivity is generally attenuated during these movements, a phenomenon known as saccadic suppression. This effect is commonly studied with large, often peripheral, stimuli presented during instructed saccades. However, little is known about how saccades modulate the foveola and how the resulting dynamics unfold during natural visual exploration. Here we measured the foveal dynamics of saccadic suppression in a naturalistic high-acuity task, a task designed after primates' social grooming, which-like most explorations of fine patterns-primarily elicits minute saccades (microsaccades). Leveraging on recent advances in gaze-contingent display control, we were able to systematically map the perisaccadic time course of sensitivity across the foveola. We show that contrast sensitivity is not uniform across this region and that both the extent and dynamics of saccadic suppression vary within the foveola. Suppression is stronger and faster in the most central portion, where sensitivity is generally higher and selectively rebounds at the onset of a new fixation. These results shed light on the modulations experienced by foveal vision during the saccade-fixation cycle and explain some of the benefits of microsaccades.

Spatiotemporal Content of Saccade Transients.

Humans use rapid gaze shifts, known as saccades, to explore visual scenes. These movements yield abrupt luminance changes on the retina, which elicit robust neural discharges at fixation onsets. Yet little is known about the spatial content of saccade transients. Here, we show that saccades redistribute spatial information within the temporal range of retinal sensitivity following two distinct regimes: saccade modulations counterbalance (whiten) the spectral density of natural scenes at low spatial frequencies and follow the external power distribution at higher frequencies. This redistribution is a consequence of saccade dynamics, particularly the speed/amplitude/duration relation known as the main sequence. It resembles the redistribution resulting from inter-saccadic eye drifts, revealing a continuum in the modulations given by different eye movements, with oculomotor transitions primarily acting by regulating the bandwidth of whitening. Our findings suggest important computational roles for saccade transients in the establishment of spatial representations and lead to testable predictions about their consequences for visual functions and encoding mechanisms.

Are the visual transients from microsaccades helpful? Measuring the influences of small saccades on contrast sensitivity.

Like all saccades, microsaccades cause both spatial and temporal changes in the input to the retina. In space, recent studies have shown that these small shifts precisely relocate a narrow (smaller than the foveola) high-acuity retinal locus on the stimulus. However, it has long been questioned whether the temporal modulations resulting from microsaccades are also beneficial for vision. To address this question, we combined spectral analysis of the visual input to the retina with measurements of contrast sensitivity in humans. Estimation of how different types of eye movements redistribute the power of an otherwise stationary stimulus shows that small saccades contribute more temporal power than ocular drift in the low-frequency range, suggesting a specific role for these movements in the encoding of low spatial frequencies. However, an influence on contrast sensitivity was only found for saccades with amplitudes larger than 30'. Contrast thresholds remained highly similar in the presence and absence of smaller saccades. Furthermore, saccades of all amplitudes, including microsaccades, were strongly suppressed during exposure to the stimulus. These findings do not support an important function of the visual transients caused by microsaccades.