Neural Mechanisms for Mid-Level Optical Flow Pattern Detection

This paper describes a new model for extracting large-field optical flow patterns to generate distributed representations of neural activation to control complex visual tasks such as 3D egomotion. The neural mechanisms draw upon experimental findings about the response properties and specificities of cells in areas V1, MT and MSTd along the dorsal pathway. Model V1 cells detect local motion estimates. Model MT cells in different pools are suggested to be selective to motion patterns integrating from V1 as well as to velocity gradients. Model MSTd cells considered here integrate MT gradient cells over a much larger spatial neighborhood to generate the observed pattern selectivity for expansion/contraction, rotation and spiral motion, providing the necessary input for spatial navigation mechanisms. Our model also incorporates feedback processing between areas V1-MT and MT-MSTd. We demonstrate that such a re-entry of context-related information helps to disambiguate and stabilize more localized processing along the primary motion pathway.

[1]  R A Andersen,et al.  Neural responses to velocity gradients in macaque cortical area MT , 1996, Visual Neuroscience.

[2]  L M Vaina,et al.  Computational modelling of optic flow selectivity in MSTd neurons. , 1998, Network.

[3]  Ohad Ben-Shahar,et al.  Geometrical Computations Explain Projection Patterns of Long-Range Horizontal Connections in Visual Cortex , 2004, Neural Computation.

[4]  G. Orban,et al.  The spatial distribution of the antagonistic surround of MT/V5 neurons. , 1997, Cerebral cortex.

[5]  Heiko Neumann,et al.  Disambiguating Visual Motion Through Contextual Feedback Modulation , 2004, Neural Computation.

[6]  E. Reed The Ecological Approach to Visual Perception , 1989 .

[7]  Arnaud Delorme,et al.  Spike-based strategies for rapid processing , 2001, Neural Networks.

[8]  T. Albright Direction and orientation selectivity of neurons in visual area MT of the macaque. , 1984, Journal of neurophysiology.

[9]  R. Wurtz,et al.  Sensitivity of MST neurons to optic flow stimuli. II. Mechanisms of response selectivity revealed by small-field stimuli. , 1991, Journal of neurophysiology.

[10]  S. Grossberg,et al.  A neural model of motion processing and visual navigation by cortical area MST. , 1999, Cerebral cortex.

[11]  Christopher C. Pack,et al.  Temporal dynamics of a neural solution to the aperture problem in visual area MT of macaque brain , 2001, Nature.

[12]  John K. Tsotsos,et al.  Attending to visual motion , 2005, Comput. Vis. Image Underst..

[13]  C. Koch,et al.  Constraints on cortical and thalamic projections: the no-strong-loops hypothesis , 1998, Nature.

[14]  Heiko Neumann,et al.  A Fast Biologically Inspired Algorithm for Recurrent Motion Estimation , 2007, IEEE Transactions on Pattern Analysis and Machine Intelligence.

[15]  M. Graziano,et al.  Tuning of MST neurons to spiral motions , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  D. Bradley,et al.  Structure and function of visual area MT. , 2005, Annual review of neuroscience.

[17]  R. Wurtz,et al.  Sensitivity of MST neurons to optic flow stimuli. I. A continuum of response selectivity to large-field stimuli. , 1991, Journal of neurophysiology.

[18]  Tim Gollisch,et al.  Modeling Single-Neuron Dynamics and Computations: A Balance of Detail and Abstraction , 2006, Science.

[19]  A. Thielscher,et al.  Neural mechanisms of cortico–cortical interaction in texture boundary detection: a modeling approach , 2003, Neuroscience.