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Prahalad, K. S.

Publications and source records attributed to Prahalad, K. S..

3 recordsLinked to original sources

Before the eye moves: microsaccade preparation expands spatial integration at the center of gaze

Fixation is often treated as a period of stable visual processing. Yet, fixation is often punctuated by frequent microsaccades that occur during tasks involving complex foveal stimuli. These small eye movements are preceded by changes in visual sensitivity, both at the upcoming movement goal and at the currently fixated location. However, previous work has largely focused on isolated stimuli, leaving unclear whether pre-microsaccadic modulations reflect changes in sensitivity alone or also alter the spatial interactions that govern object recognition. Visual crowding provides a direct test of this question because it depends on the integration and segregation of nearby features and constrains recognition even within the foveola. Using high-precision Dual Purkinje Image eye tracking with retinally contingent stimulus delivery, we measured acuity and crowding thresholds at the preferred locus of fixation (PLF), the starting point of the impending gaze shift, while observers either maintained fixation or prepared to execute a microsaccade to a cued location. Unflanked acuity at the PLF remained stable across conditions. In contrast, crowding strength increased during the pre-microsaccadic interval, indicating an expansion of the foveal crowding zone. These results show that microsaccade preparation alters spatial integration at the starting point of the movement, increasing crowding even when sensitivity to isolated stimuli remains unchanged. Thus, microsaccades reshape foveal vision not only by modulating visual discrimination at the movement goal, but also by changing how nearby features are integrated and segregated before the eyes move. Significance StatementVision is often assumed to be most stable when gaze is fixed. Yet the eyes are never truly still, and the brain continually prepares small movements that shape perception before they occur. This study shows that such preparation changes how visual information is organized at the very center of gaze. Upcoming eye movements do not simply alter sensitivity to isolated objects; instead, they change how nearby features are integrated. These findings reveal that fine spatial vision and object recognition depends not only on what falls on the retina or on subsequent cortical processing but also on what the eyes are preparing to do next.

neuroscience↗

Distinct growth regimes govern crowding in foveal and extrafoveal vision

Visual crowding--where object recognition is impaired by nearby stimuli--is a well-documented phenomenon in the visual periphery, thought to reflect fundamental processes of grouping and segmentation. A hallmark of crowding is its spatial extent increasing linearly with eccentricity, as described by Boumas law, reflecting retinal convergence and cortical magnification. Although crowding is typically studied in the periphery--and Boumas law predicts no crowding at the center of gaze--it occurs even foveally. Within the foveola, the central 1 deg of the visual field, characterized by peak visual acuity and largely one-to-one connectivity between photoreceptors and ganglion cells, the Bouma law breaks and the extent of crowding is expected to remain constant with eccentricity. Yet, whether crowding varies at this fine spatial scale remains unknown. To investigate this, we combined high-resolution eye tracking with a gaze-contingent display system to precisely localize gaze and measure crowding thresholds at multiple foveolar eccentricities. Our results reveal that crowding does increase linearly within the foveola, but at a rate significantly slower--approximately 3.5 times-than in the extrafovea. By showing that even within the highest-acuity region of the visual field, spatial integration zones are not fixed but change with eccentricity these findings challenge the view of the central fovea as a spatially uniform processing zone and demonstrate that crowding at this scale follows a distinct regime. SignificanceWhen we view objects in clutter, recognition declines--a phenomenon known as crowding. This effect increases with distance from the center of gaze, following Boumas law, which predicts little or no crowding at the foveas center. As this law breaks at the center of gaze, it has been hypothesized that around this region, crowding remains constant with eccentricity. Using high-resolution eyetracking, we show that even within the central 0.4{degrees} of the visual field, crowding increases steadily with minute stimulus offsets from the point of fixation. This growth is much slower than in peripheral vision, revealing a distinct crowding regime in the foveola, likely reflecting cortical and retinal differences. Our findings offer new insights into the fine-scale organization of spatial vision.

neuroscience↗

Subfoveal scotomas trigger fine-scale fixation reorganization: insights from retinal imaging and retinal-contingent stimulation

Fine spatial vision relies on the foveola, the 1-degree retinal region with highest cone density. Despite its importance, the relationship between retinal anatomy, fixational behavior, and visual perception in the foveola is not fully understood. Using an Adaptive Optics Scanning Light Ophthalmoscope for high-resolution retinal imaging and stimulation, we studied the effect of a simulated subfoveolar ({approx}0.03 degrees2) scotoma on fine spatial vision and fixation behavior in healthy observers. Our findings show that the visuomotor system adapts to the scotoma with striking precision by shifting the preferred locus of fixation in a systematic fashion by minute ({approx}5 arcmin) amounts to bring stimuli into a region of visibility. These results reveal an unprecedented level of fine-scale plasticity in the human visuomotor system. Interestingly, this new retinal locus of fixation is characterized by lower cone density among those surrounding the scotoma, indicating that factors beyond spatial sampling maximization influence these fine-scale adjustments.

neuroscience↗