Mapping residual stereopsis in macular degeneration.

Individuals with macular degeneration typically lose vision in the central region of one or both eyes. A binocular scotoma occurs when vision loss occurs in overlapping locations in both eyes, but stereopsis is impacted even in the non-overlapping region wherever the visual field in either eye is affected. We used a novel stereoperimetry protocol to measure local stereopsis across the visual field (up to 25° eccentricity) to determine how locations with functional stereopsis relate to the scotomata in the two eyes. Participants included those with monocular or binocular scotomata and age-matched controls with healthy vision. Targets (with or without depth information) were presented on a random dot background. Depth targets had true binocular disparity of 20' (crossed), whereas non-depth targets were defined by monocular cues such as contrast and dot density. Participants reported target location and whether it was in depth or flat. Local depth sensitivity (d') estimates were then combined to generate a stereopsis map. This stereopsis map was compared to the union of the monocular microperimetry estimates that mapped out the functional extent of the scotoma in each eye. The "union" prediction aligned with residual stereopsis, showing impaired stereopsis within this region and residual stereopsis outside this region. Importantly, the stereoblind region was typically more extensive than the binocular scotoma defined by the intersection (overlap) of the scotomata. This explains why individuals may have intact binocular visual fields but be severely compromised in tasks of daily living that benefit from stereopsis, such as eye-hand coordination and navigation.

Saccades during visual search in macular degeneration.

Macular degeneration (MD) compromises both high-acuity vision and eye movements when the foveal regions of both eyes are affected. Individuals with MD adapt to central field loss by adopting a preferred retinal locus (PRL) for fixation. Here, we investigate how individuals with bilateral MD use eye movements to search for targets in a visual scene under realistic binocular viewing conditions. Five individuals with binocular scotomata, 3 individuals with monocular scotomata and 6 age-matched controls participated in our study. We first extensively mapped the binocular scotoma with an eyetracker, while fixation was carefully monitored (Vullings & Verghese, 2020). Participants then completed a visual search task where 0, 1, or 2 Gaussian blobs were distributed randomly across a natural scene. Participants were given 10 s to actively search the display and report the number of blobs. An analysis of saccade characteristics showed that individuals with binocular scotomata made more saccades in the direction of their scotoma than controls for the same directions. Saccades in the direction of the scotoma were typically of small amplitude, and did not fully uncover the region previously hidden by the scotoma. Rather than make more saccades to explore this hidden region, participants frequently made saccades back toward newly uncovered regions. Backward saccades likely serve a similar purpose to regressive saccades exhibited during reading in MD, by inspecting previously covered regions near the direction of gaze. Our analysis suggests that the higher prevalence of backward saccades in individuals with binocular scotomata might be related to the PRL being adjacent to the scotoma.

Saccadic contributions to smooth pursuit in macular degeneration.

Saccades during smooth pursuit can help bring the fovea on target, particularly in cases of low pursuit gain. Individuals with macular degeneration often suffer damage to the central retina including the fovea, which impacts oculomotor function such as fixation, saccadic and smooth pursuit eye movements. We hypothesized that these oculomotor changes in macular degeneration (MD) would make saccades less appropriately directed (even if more numerous). To investigate saccades during pursuit in MD, we conducted a quantitative analysis of smooth pursuit eye movement data from a prior study, Vision Research 141 (2017) 181-190. Here we examined saccade frequency, magnitude, and direction across viewing conditions for MD and control participants during pursuit of a target moving in a modified step-ramp paradigm. Individuals with MD had more variability in saccade directions that included directions orthogonal to the target trajectory. PRL eccentricity significantly correlated with increases in saccades in non-target directions during smooth pursuit. These results suggest that a large number of saccades during pursuit in MD participants are unlikely to be catch-up saccades that serve to keep the eye on the target.

Memory Fidelity Reveals Qualitative Changes in Interactions Between Items in Visual Working Memory.

Memory for objects in a display sometimes reveals attraction-the objects are remembered as more similar to one another than they actually were-and sometimes reveals repulsion-the objects are remembered as more different from one another. The conditions that lead to these opposing memory biases are poorly understood; there is no theoretical framework that explains these contrasting dynamics. In three experiments (each N = 30 adults), we demonstrate that memory fidelity provides a unifying dimension that accommodates the existence of both types of visual working memory interactions. We show that either attraction or repulsion can arise simply as a function of manipulations of memory fidelity. We also demonstrate that subjective ratings of fidelity predict the presence of attraction or repulsion on a trial-by-trial basis. We discuss how these results bear on computational models of visual working memory and contextualize these results within the literature of attraction and repulsion effects in long-term memory and perception.

Irrelevant features of distractors in intervening visual search tasks cause active visual working memory interference - the more difficult the search task, the more interference it causes.

Visual working memory (VWM) content disrupts visual search performance when there is a singleton in the search array that is similar to the content in VWM, even when this singleton is task irrelevant. Typically, the memory-similar singleton captures attention, which results in slower search performance for memory-similar conditions compared to conditions where memory-similar content is absent. Recently, it has also been shown that VWM content may be affected when memory-similar stimuli are processed. Specifically, it appears that VWM representations bias toward memory-similar information that is processed but not memory-dissimilar information. Here, we test whether the bias caused by processing memory-similar information is an active interference process (growing with engagement with the memory-similar stimuli) or a passive interference process (indifferent to the engagement with memory-similar stimuli). To test this, observers were tasked with memorizing a single color followed by a search task. The search task was either easy or difficult, and the search items could either be memory-similar or memory-dissimilar. Critically, the target in the search task was defined by its shape, so the color of the search items was irrelevant to the search task. At the end of each trial, participants reported the color in memory using a continuous report color wheel. The results showed that VWM representations drifted towards the irrelevant color of the search items in the memory-similar conditions, and this effect was larger in the difficult search condition. The results provide evidence that VWM representations receive active interference from processing memory-similar stimuli.