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Victor, J.

Publications and source records attributed to Victor, J..

2 recordsLinked to original sources

Contrast sensitivity reveals an oculomotor strategy for temporally encoding space

The contrast sensitivity function (CSF), how sensitivity varies with the spatial frequency of the stimulus, is a fundamental assessment of visual performance. The CSF is generally assumed to be determined by low-level sensory processes. However, the sensitivities of neurons in the early visual pathways, as measured in experiments with immobilized eyes, diverge from psychophysical CSF measurements in primates. Under natural viewing conditions, as in typical psychophysical measurements, humans continually move their eyes, drifting in a seemingly erratic manner even when looking at a fixed point. Here, we show that the resulting transformation of the visual scene into a spatiotemporal flow on the retina constitutes a processing stage that reconciles human CSF and the response characteristics of retinal ganglion cells under a broad range of conditions. Our findings suggest a fundamental integration between perception and action: eye movements work synergistically with the sensitivities of retinal neurons to encode spatial information.

neuroscience

Neural computations combine low- and high-order motion cues similarly, in dragonfly and monkey

Visual motion analysis is fundamental to survival across the animal kingdom. In insects, our understanding of the underlying computations has centered on the Hassenstein-Reichardt motion detector, which computes two-point cross-correlation via multiplication; in mammalian cortex, it is postulated that a similar signal is computed by comparing matched squaring operations. Both of these operations are difficult to implement biophysically in a precise fashion; moreover, they fail to detect the more complex multipoint local motion cues present in the visual environment. Here, via single-unit recordings in two visual specialists, dragonfly \"(Odonata)\" and macaque, and via model simulations, we show that neuronal computations are not simply approximations to idealized behaviors forced by biological constraints, but rather, are signatures of a common computational strategy to capture multiple local motion cues. The similarity of motion computations at the neuronal level in the brains of two extremely dissimilar animals, with evolutionary divergence of over 700 Myr1, suggests convergence on a common computational scheme for detecting visual motion.

neuroscience