Boundary cue invariance in cortical orientation maps.

We effortlessly perceive oriented boundaries defined by either luminance changes ('first-order' cues) or texture variations ('second-order' cues). Many neurons in mammalian visual cortex show orientation preference to both types of boundaries, but it is uncertain how they contribute to perceptual orientation cue-invariance at the neuronal population level. Using optical imaging in cat A 18, we observed highly similar orientation preference maps to first-order and a variety of second-order visual stimuli. Thus the neuronal representation of coarse-scale boundary orientation appears to be invariant to the characteristics (including local orientation) of the fine-scale textures by which those boundaries are defined. A common feature of second-order visual stimuli is that modulation shifts their Fourier energy for boundary orientation to the higher spatial frequencies of their constituent textures - our results suggest a common neural mechanism (demodulation) mediating visual processing of many kinds of texture boundary. The similarity between orientation maps to different stimuli implies that second-order responsive neurons are homogeneously distributed across the cortical surface. Such homogeneously cue-invariant orientation representation could provide a neural substrate for perceptual form-cue invariance, and reflect an optimal organization for encoding orientation information in natural scenes.