Sereno, 1987) showed that a feedforward network with area VIlike input-layer units and a Hebb rule can develop area MTlike second layer units that solve the aperture problem for pattern motion. The present study extends this earlier work to more complex motions. Saito et al. (1986) showed that neurons with large receptive fields in macaque visual area MST are sensitive to different senses of rotation and dilation, irrespective of the receptive field location of the movement singularity. A network with an MTlike second layer was trained and tested on combinations of rotating, dilating, and translating patterns. Third-layer units learn to detect specific senses of rotation or dilation in a position-independent fashion, despite having position-dependent direction selectivity within their receptive fields.

Sereno, 1987) showed that a feedforward network with area VIlike input-layer units and a Hebb rule can develop area MTlike second layer units that solve the aperture problem for pattern motion. The present study extends this earlier work to more complex motions. Saito et al. (1986) showed that neurons with large receptive fields in macaque visual area MST are sensitive to different senses of rotation and dilation, irrespective of the receptive field location of the movement singularity. A network with an MTlike second layer was trained and tested on combinations of rotating, dilating, and translating patterns. Third-layer units learn to detect specific senses of rotation or dilation in a position-independent fashion, despite having position-dependent direction selectivity within their receptive fields.

Linsker's model was presented with input patterns each consisting

The primate visual system learns to recognize the true direction of pattern motion using local detectors only capable of detecting the component of motion perpendicular to the orientation of the moving edge. A multilayer feedforward network model similar to Linsker's model was presented with input patterns each consisting of randomly oriented contours moving in a particular direction. Input layer units are granted component direction and speed tuning curves similar to those recorded from neurons in primate visual area VI that project to area MT. The network is trained on many such patterns until most weights saturate. A proportion of the units in the second layer solve the aperture problem (e.g., show the same direction-tuning curve peak to plaids as to gratings), resembling pattern-direction selective neurons, which ftrst appear inareaMT.