IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1002405.html
   My bibliography  Save this article

Cortical Surround Interactions and Perceptual Salience via Natural Scene Statistics

Author

Listed:
  • Ruben Coen-Cagli
  • Peter Dayan
  • Odelia Schwartz

Abstract

Spatial context in images induces perceptual phenomena associated with salience and modulates the responses of neurons in primary visual cortex (V1). However, the computational and ecological principles underlying contextual effects are incompletely understood. We introduce a model of natural images that includes grouping and segmentation of neighboring features based on their joint statistics, and we interpret the firing rates of V1 neurons as performing optimal recognition in this model. We show that this leads to a substantial generalization of divisive normalization, a computation that is ubiquitous in many neural areas and systems. A main novelty in our model is that the influence of the context on a target stimulus is determined by their degree of statistical dependence. We optimized the parameters of the model on natural image patches, and then simulated neural and perceptual responses on stimuli used in classical experiments. The model reproduces some rich and complex response patterns observed in V1, such as the contrast dependence, orientation tuning and spatial asymmetry of surround suppression, while also allowing for surround facilitation under conditions of weak stimulation. It also mimics the perceptual salience produced by simple displays, and leads to readily testable predictions. Our results provide a principled account of orientation-based contextual modulation in early vision and its sensitivity to the homogeneity and spatial arrangement of inputs, and lends statistical support to the theory that V1 computes visual salience. Author Summary: One of the most important and enduring hypotheses about the way that mammalian brains process sensory information is that they are exquisitely attuned to the statistical structure of the natural world. This allows them to come, over the course of development, to represent inputs in a way that reflects the facets of the environment that were responsible. We focus on the case of information about the local orientation of visual input, a basic level feature for which a wealth of phenomenological observations are available to constrain and validate computational models. We suggest a new account which focuses on the statistics of orientations at nearby locations in visual space, and captures data on how such contextual information modulates both the responses of neurons in the primary visual cortex, and the corresponding psychophysical percepts. Our approach thus helps elucidate the computational and ecological principles underlying contextual processing in early vision; provides a number of predictions that are readily testable with existing experimental approaches; and indicates a possible route for examining whether similar computational principles and operations also support higher-level visual functions.

Suggested Citation

  • Ruben Coen-Cagli & Peter Dayan & Odelia Schwartz, 2012. "Cortical Surround Interactions and Perceptual Salience via Natural Scene Statistics," PLOS Computational Biology, Public Library of Science, vol. 8(3), pages 1-18, March.
  • Handle: RePEc:plo:pcbi00:1002405
    DOI: 10.1371/journal.pcbi.1002405
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1002405
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1002405&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1002405?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Jeffrey L Gauthier & Greg D Field & Alexander Sher & Martin Greschner & Jonathon Shlens & Alan M Litke & E J Chichilnisky, 2009. "Receptive Fields in Primate Retina Are Coordinated to Sample Visual Space More Uniformly," PLOS Biology, Public Library of Science, vol. 7(4), pages 1-9, April.
    2. Yan Karklin & Michael S. Lewicki, 2009. "Emergence of complex cell properties by learning to generalize in natural scenes," Nature, Nature, vol. 457(7225), pages 83-86, January.
    3. Jonathan B. Levitt & Jennifer S. Lund, 1997. "Contrast dependence of contextual effects in primate visual cortex," Nature, Nature, vol. 387(6628), pages 73-76, May.
    4. Uri Polat & Keiko Mizobe & Mark W. Pettet & Takuji Kasamatsu & Anthony M. Norcia, 1998. "Collinear stimuli regulate visual responses depending on cell's contrast threshold," Nature, Nature, vol. 391(6667), pages 580-584, February.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Jonathan J Hunt & Peter Dayan & Geoffrey J Goodhill, 2013. "Sparse Coding Can Predict Primary Visual Cortex Receptive Field Changes Induced by Abnormal Visual Input," PLOS Computational Biology, Public Library of Science, vol. 9(5), pages 1-17, May.
    2. Laurence Aitchison & Máté Lengyel, 2016. "The Hamiltonian Brain: Efficient Probabilistic Inference with Excitatory-Inhibitory Neural Circuit Dynamics," PLOS Computational Biology, Public Library of Science, vol. 12(12), pages 1-24, December.

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Li Zhaoping & Li Zhe, 2015. "Primary Visual Cortex as a Saliency Map: A Parameter-Free Prediction and Its Test by Behavioral Data," PLOS Computational Biology, Public Library of Science, vol. 11(10), pages 1-39, October.
    2. Jörn-Philipp Lies & Ralf M Häfner & Matthias Bethge, 2014. "Slowness and Sparseness Have Diverging Effects on Complex Cell Learning," PLOS Computational Biology, Public Library of Science, vol. 10(3), pages 1-11, March.
    3. Sophie Hall & Patrick Bourke & Kun Guo, 2014. "Low Level Constraints on Dynamic Contour Path Integration," PLOS ONE, Public Library of Science, vol. 9(6), pages 1-9, June.
    4. Manuel Schottdorf & Stephen J Eglen & Fred Wolf & Wolfgang Keil, 2014. "Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?," PLOS ONE, Public Library of Science, vol. 9(1), pages 1-18, January.
    5. Yoram S Bonneh & Tobias H Donner & Alexander Cooperman & David J Heeger & Dov Sagi, 2014. "Motion-Induced Blindness and Troxler Fading: Common and Different Mechanisms," PLOS ONE, Public Library of Science, vol. 9(3), pages 1-8, March.
    6. Li Zhaoping & Li Jingling, 2008. "Filling-In and Suppression of Visual Perception from Context: A Bayesian Account of Perceptual Biases by Contextual Influences," PLOS Computational Biology, Public Library of Science, vol. 4(2), pages 1-13, February.
    7. Udo A Ernst & Sunita Mandon & Nadja Schinkel–Bielefeld & Simon D Neitzel & Andreas K Kreiter & Klaus R Pawelzik, 2012. "Optimality of Human Contour Integration," PLOS Computational Biology, Public Library of Science, vol. 8(5), pages 1-17, May.
    8. Iris I A Groen & Sennay Ghebreab & Victor A F Lamme & H Steven Scholte, 2012. "Spatially Pooled Contrast Responses Predict Neural and Perceptual Similarity of Naturalistic Image Categories," PLOS Computational Biology, Public Library of Science, vol. 8(10), pages 1-16, October.
    9. Qiang Sang & Biao Cai & Hao Chen, 2017. "Contour detection improved by context-adaptive surround suppression," PLOS ONE, Public Library of Science, vol. 12(7), pages 1-13, July.
    10. Jeffrey D Fitzgerald & Ryan J Rowekamp & Lawrence C Sincich & Tatyana O Sharpee, 2011. "Second Order Dimensionality Reduction Using Minimum and Maximum Mutual Information Models," PLOS Computational Biology, Public Library of Science, vol. 7(10), pages 1-9, October.
    11. Yajie Liang & Rongwen Lu & Katharine Borges & Na Ji, 2023. "Stimulus edges induce orientation tuning in superior colliculus," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    12. Xaq Pitkow & Haim Sompolinsky & Markus Meister, 2007. "A Neural Computation for Visual Acuity in the Presence of Eye Movements," PLOS Biology, Public Library of Science, vol. 5(12), pages 1-14, December.
    13. Qianli Yang & Edgar Walker & R. James Cotton & Andreas S. Tolias & Xaq Pitkow, 2021. "Revealing nonlinear neural decoding by analyzing choices," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
    14. Boris Vladimirskiy & Robert Urbanczik & Walter Senn, 2015. "Hierarchical Novelty-Familiarity Representation in the Visual System by Modular Predictive Coding," PLOS ONE, Public Library of Science, vol. 10(12), pages 1-19, December.
    15. Malte Persike & Günter Meinhardt, 2015. "Effects of Spatial Frequency Similarity and Dissimilarity on Contour Integration," PLOS ONE, Public Library of Science, vol. 10(6), pages 1-19, June.
    16. Laurence Aitchison & Máté Lengyel, 2016. "The Hamiltonian Brain: Efficient Probabilistic Inference with Excitatory-Inhibitory Neural Circuit Dynamics," PLOS Computational Biology, Public Library of Science, vol. 12(12), pages 1-24, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1002405. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.