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Simoncelli, E.

Publications and source records attributed to Simoncelli, E..

2 recordsLinked to original sources

Foveated metamers of the early visual system

The ability of humans to discriminate and identify spatial patterns varies across the visual field, and is generally worse in the periphery than in the fovea. This decline in performance is revealed in many kinds of tasks, from detection to recognition. A parsimonious hypothesis is that the representation of any visual feature is blurred (spatially averaged) by an amount that differs for each feature, but that in all cases increases with eccentricity. Here, we examine models for two such features: local luminance and spectral energy. Each model averages the corresponding feature in pooling windows whose diameters scale linearly with eccentricity. We performed perceptual experiments with synthetic stimuli to determine the largest window scaling for which human and model discrimination abilities match (the "critical" scaling). We used much larger stimuli than those of previous studies, subtending 53.6 by 42.2 degrees of visual angle. We found that the critical scaling for the luminance model was approximately one-fourth that of the energy model and, consistent with earlier studies, that the estimated critical scaling value was smaller when discriminating a synthesized stimulus from a natural image than when discriminating two synthesized stimuli. Moreover, we found that initializing the generation of the synthesized images with natural images reduced the critical scaling value when discriminating two synthesized stimuli, but not when discriminating a synthesized from a natural image stimulus. Together, the results show that critical scaling is strongly affected by the image statistic (pooled luminance vs. spectral energy), the comparison type (synthesized vs. synthesized or synthesized vs. natural), and the initialization image for synthesis (white noise vs natural image). We offer a coherent explanation for these results in terms of alignments and misalignments of the models with human perceptual representations.

neuroscience↗

Compound stimuli reveal the structure of visual motion selectivity in macaque MT neurons

Motion selectivity in primary visual cortex (V1) is approximately separable in orientation, spatial frequency, and temporal frequency (\"frequency-separable\"). Models for area MT neurons posit that their selectivity arises by combining direction-selective V1 afferents whose tuning is organized around a tilted plane in the frequency domain, specifying a particular direction and speed (\"velocity-separable\"). This construction explains \"pattern direction selective\" MT neurons, which are velocity-selective but relatively invariant to spatial structure, including spatial frequency, texture and shape. Surprisingly, when tested with single drifting gratings, most MT neurons responses are fit equally well by models with either form of separability. However, responses to plaids (sums of two moving gratings) tend to be better described as velocity-separable, especially for pattern neurons. We conclude that direction selectivity in MT is primarily computed by summing V1 afferents, but pattern-invariant velocity tuning for complex stimuli may arise from local, recurrent interactions.\n\nSignificance StatementHow do sensory systems build representations of complex features from simpler ones? Visual motion representation in cortex is a well-studied example: the direction and speed of moving objects, regardless of shape or texture, is computed from the local motion of oriented edges. Here we quantify tuning properties based on single-unit recordings in primate area MT, then fit a novel, generalized model of motion computation. The model reveals two core properties of MT neurons -- speed tuning and invariance to local edge orientation -- result from a single organizing principle: each MT neuron combines afferents that represent edge motions consistent with a common velocity, much as V1 simple cells combine thalamic inputs consistent with a common orientation.

neuroscience↗