Cited by 426Visual perception and processing mechanismsNeural dynamics and brain functionNeural Networks and Applications

A Neural Model of Contour Integration in the Primary Visual Cortex

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Li, Zhaoping·1998·Neural Computation

Abstract

Experimental observations suggest that contour integration may take place in V1. However, there has yet to be a model of contour integration that uses only known V1 elements, operations, and connection patterns.This article introduces such a model, using orient ation selective cells, local cortical circuits, and horizontal intracortical connections. The model is composed of recurrently connected excitatory neurons and inhibitory interneurons, receiving visual input via oriented receptive fields resembling those found in primary visual cortex. Intracortical interactions modify initial activity patterns from input, selectively amplifying the activities of edges that form smooth contours in the image. The neural activities produced by such interactions are oscillatory and edge segments within a contour oscillate in synchrony. It is shown analytically and empirically that the extent of contour enhancement and neural synchrony increases with the smoothness, length, and closure of contours, as observed in experiments on some of these phenomena. In addition, the model incorporates a feedback mechanism that allows higher visual centers selectively to enhance or suppress sensitivities to given contours, effectively segmenting one from another. The model makes the testable prediction that the horizontal cortical connections are more likely to target excitatory (or inhibitory) cells when the two linked cells have their preferred orientation aligned with (or orthogonal to) their relative receptive field center displacements.

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Crossref · 10.1162/089976698300017557

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  • Instead of being the first stage in a feedforward pipeline, V1 is better described as the unique high-resolution buffer in the visual system for geometric calculations.

    “This led us to propose that, instead of being the first stage in a feedforward pipeline, 13 V1 is better described as the unique high-resolution buffer in the visual system for geometric calculations. 40,41”

    From Hierarchical Bayesian inference in the visual cortex (2003) · cites this paper as [41]

    The Introduction and §4.1 describe V1 as performing local contour enhancement through recurrent interactions, rather than merely passing visual input forward. Section 3.7 also models feedback from higher visual areas. The paper does not describe V1 as the visual system’s unique high-resolution buffer or extend its contour-enhancement model to geometric calculations generally. (LLM, conf=0.82)

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Research works printed but not linked: 34

  1. Douglas, R. J., & Martin, K. A. (1990). Neocortex. In G. M. Shepherd (Ed.), Synaptic organization of the brain (3rd Ed.). New York: Oxford University Press.
  2. Field, D. J., Hayes, A., & Hess, R. F. (1993). Contour integration by the human visual system: Evidence for a local "association field." Vision Res., 33(2), 173- 193.
  3. Freeman, W. J. (1987). Simulation of chaotic EEG patterns with a dynamic model of the olfactory system. Biol. Cybern., 56(2-3), 139-150.
  4. Gilbert, C. D. (1992). Horizontal integration and cortical dynamics. Neuron, 9(1), 1-13.
  5. Gilbert, C. D., & Wiesel, T. N. (1983). Clustered intrinsic connections in cat visual cortex. J. Neurosci., 3(5), 1116-1133.
  6. Gilbert, C. D., & Wiesel, T. N. (1989). Columnar specificity of intrinsic horizontal and corticocortical connections in cat visual cortex. J. Neurosci., 9(7), 2432- 2442.
  7. Gilbert, C. D., & Wiesel, T. N. (1990). The influence of contextual stimuli on the orientation selectivity of cells in primary visual cortex of the cat. Vision Res., 30(11), 1689-1701.
  8. Gray, C. M., & Singer, W. (1989). Stimulus-specific neuronal oscillations in orien- tation columns of cat visual cortex. Proc. Natl. Acad. Sci. USA, 86, 1698-1702.
  9. Grosof, D. H., Shapley, R. M., & Hawken, M. J. (1993). Macaque V1 neurons can signal "illusory" contours. Nature, 365(6446), 550-552.
  10. Grossberg, S., & Mingolla, E. (1985). Neural dynamics of perceptual group- ing: Textures, boundaries, and emergent segmentations. Percept. Psychophys., 38(2), 141-171.
  11. Guy, G., & Medioni, G. (1993). Inferring global perceptual contours from local features. In Proc. IEEE CVPR (pp. 786-787).
  12. Heitger, F., & von der Heydt, R. (1993). A computational model of neural contour processing: Figure-ground segregation and illusory contours. In Proc. of 4th Intl. Conf. on Computer Vision (pp. 32-40).
  13. Hirsch, J. A., & Gilbert, C. D. (1991). Synaptic physiology of horizontal connec- tions in the cat's visual cortex. J. Neurosci., 11(6), 1800-1809.
  14. Hummel, R., & Zucker, S. W. (1983). On the foundation of relaxation labeling processes. IEEE Transactions on Pattern Analysis and Machine Intelligence, 5, 267-287.
  15. Kapadia, M. K., Ito, M., Gilbert, C. D., & Westheimer, G. (1995). Improvement in visual sensitivity by changes in local context: Parallel studies in human observers and in V1 of alert monkeys. Neuron, 15(4), 843-856.
  16. Kovacs, I., & Julesz, B. (1993). A closed curve is much more than an incomplete one: Effect of closure in figure-ground segmentation. Proc. Natl. Acad. Sci. USA, 15, 90(16), 7495-7497.
  17. Lamme, V. A. (1995). The neurophysiology of figure-ground segregation in pri- mary visual cortex. Journal of Neuroscience, 15(2), 1605-1615.
  18. Li, Zhaoping. (1997). Primary cortical dynamics for visual computation. In K-Y. M. Wong, I. King, & D-Y. Yeung (Eds.) Theoretical Aspects of Neural Computation workshop, Hong Kong: Springer-Verlag.
  19. Li, Zhaoping, & Hopfield, J. J. (1989). Modeling the olfactory bulb and its neural oscillatory processings. Biol. Cybern., 61(5), 379-392.
  20. Maffei, L., & Fiorentini, A. (1976). The unresponsive regions of visual cortical receptive fields. Vision Res., 16(10), 1131-1139.
  21. Malach, R., Amir, Y., Harel, M., & Grinvald, A. (1993). Relationship between intrinsic connections and functional architecture revealed by optical imaging and in vivo targeted biocyting injections in primate striate cortex. Proc. Natl. Acad. Sci. USA, 90, 10469-10473.
  22. Motter, B. C. (1993). Focal attention produces spatially selective processing in visual cortical areas V1, V2, and V4 in the presence of competing stimuli. J. Neurophysiol., 70(3), 909-919.
  23. Polat, U., & Sagi, D. (1994). The architecture of perceptual spatial interactions. Vision Res., 34(1), 73-78.
  24. Rockland, K. S., & Lund, J. S. (1983). Intrinsic laminar lattice connections in primate visual cortex. J. Comp. Neurol., 216(3), 303-318.
  25. Shashua, A., & Ullman, S. (1988). Structural saliency. Proceedings of the Interna- tional Conference on Computer Vision (pp. 482-488).
  26. Shepherd, G. M. (1990). Synaptic organization of the brain (3rd ed.) New York: Oxford University Press.
  27. Somers, D. C., Nelson, S. B., & Sur, M. (1995). An emergent model of orientation selectivity in cat visual cortical simple cells. Journal of Neuroscience, 15(8), 5448-5465.
  28. Somers, D. C., Todorov, E. V., Siapas, A. G., & Sur, M. (1995). Vector-based inte- gration of local and long-range information in visual cortex (AI Memo. No. 1556). Cambridge, MA: MIT.
  29. Sporns, O., Tononi, G., & Edelman, G. M. (1991). Modeling perceptual grouping and figure-ground segregation by means of reentrant connections. Proc. Natl. Acad. Sci. USA, 88, 129-133.
  30. Ts'o, D. Y., Gilbert, C. D., & Wiesel, T. N. (1986). Relationships between horizontal interactions and functional architecture in cat striate cortex as revealed by cross-correlation analysis. J. Neurosci., 6(4), 1160-1170.
  31. Valverde, F. (1985). The organization principles of the primary visual cortex in the monkey. In A. Peters & E. G. Jones (Eds.), Cerebral cortex (pp. 207-258). New York: Plenum Press.
  32. van Essen, D. (1985). Functional organization of primate visual cortex. In A. Pe- ters & E. G. Jones (Eds.), Cerebral cortex (pp. 259-329). New York: Plenum Press.
  33. Williams, L. R., & Jacobs, D. W. (1996). Local parallel computation of stochastic completion fields. In Proc. IEEE CVPR (pp. 161-168).
  34. Yen, S.-C., & Finkel, L. H. (1997). Salient contour extraction by temporal binding in a cortically-based network. In M. C. Mozer, M. I. Jordan, & T. Petsche (Eds.), Neural Information Processing Systems 9. Cambridge, MA: MIT Press.

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Authors
Li, Z.
Affiliations
Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong
Venue
Neural Computation
Published
1998-05-01
Volume
10
Issue
4
Pages
903-940
ISSN
  • 0899-7667 (ISSN-L)
  • 1530-888X
OpenAlex
W2134394617
Cited by
426
References
2
Citations by year
2026: 3 · 2025: 9 · 2024: 12 · 2023: 7 · 2022: 5 · 2021: 6 · 2020: 14 · 2019: 7 · 2018: 10 · 2017: 18 · 2016: 12 · 2015: 13 · 2014: 31 · 2013: 15 · 2012: 10
FWCI
11.68
Type
journal article
Language
en
Open access
Locations
  • Neural Computation (publishedVersion)
  • PubMed (publishedVersion)
  • UCL Discovery (University College London) (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
  • Physical Sciences › Computer Science › Artificial Intelligence › Neural Networks and Applications
Keywords
contour integration, primary visual cortex, recurrent neural networks, inhibitory interneurons, neuronal synchronization, contour closure, feedback mechanisms, contour segmentation, receptive fields
MeSH terms
Feedback, Form Perception, Mental Processes, Models, Neurological, Oscillometry, Time Factors, Visual Cortex, Linear Models

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