Contextual masking of oriented lines: interactions between surface segmentation cues.

The ability of human observers to detect and discriminate a single feature of a visual image deteriorates markedly when the targeted feature is surrounded by others of a similar kind. This perceptual masking is mirrored by the suppressive effects of surround stimulation on the responses of neurons in primary visual cortex (area V1). Both perceptual and neuronal masking effects are partially relieved, however, if the targeted image feature is distinguished from surrounding features along some dimension, such as contour orientation. Masking relief is likely to play an important role in perceptual segmentation of complex images. Because dissimilar surfaces usually differ along multiple feature dimensions, we tested the possibility that those differences may influence segmentation in an invariant manner. As expected, we found that the presence of surrounding features resulted in perceptual masking and neuronal response suppression in area V1, but that either orientation or contrast polarity differences between the target and surrounding features was sufficient to partially relieve these effects. Simultaneous differences along both dimensions, however, yielded no greater relief from masking than did either difference alone. Although the averaged neuronal effects of orientation polarity cues were thus invariant, the time course over which these effects emerged after each stimulus appearance was different for the two cues. These findings refine our understanding of the functions of nonclassical receptive fields, and they support a key role for V1 neurons in surface segmentation.

[1]  R. Sekuler,et al.  Spatial and temporal determinants of visual backward masking. , 1965, Journal of experimental psychology.

[2]  D. Levi,et al.  The effect of similarity and duration on spatial interaction in peripheral vision. , 1994, Spatial vision.

[3]  J. Beck Similarity grouping and peripheral discriminability under uncertainty. , 1972, The American journal of psychology.

[4]  A. Treisman,et al.  A feature-integration theory of attention , 1980, Cognitive Psychology.

[5]  G Westheimer,et al.  Patterns That Impair Discrimination of Line Orientation in Human Vision , 1996, Perception.

[6]  C. Li,et al.  Extensive integration field beyond the classical receptive field of cat's striate cortical neurons--classification and tuning properties. , 1994, Vision research.

[7]  Victor A. F. Lamme,et al.  Synchrony and covariation of firing rates in the primary visual cortex during contour grouping , 2004, Nature Neuroscience.

[8]  Thomas D. Albright,et al.  Why do things look as they do? , 1994, Trends in Neurosciences.

[9]  John H. R. Maunsell,et al.  The visual field representation in striate cortex of the macaque monkey: Asymmetries, anisotropies, and individual variability , 1984, Vision Research.

[10]  J. Horton,et al.  Receptive field properties in the cat's lateral geniculate nucleus in the absence of on-center retinal input , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  E. V. Famiglietti,et al.  Structural basis for ON-and OFF-center responses in retinal ganglion cells. , 1976, Science.

[12]  R. Shapley,et al.  Contextual influences on orientation discrimination: binding local and global cues , 2001, Vision Research.

[13]  Peter H. Schiller,et al.  The ON and OFF channels of the visual system , 1992, Trends in Neurosciences.

[14]  D. Robinson,et al.  A METHOD OF MEASURING EYE MOVEMENT USING A SCLERAL SEARCH COIL IN A MAGNETIC FIELD. , 1963, IEEE transactions on bio-medical engineering.

[15]  James R. Bergen,et al.  Parallel versus serial processing in rapid pattern discrimination , 1983, Nature.

[16]  DH Hubel,et al.  Psychophysical evidence for separate channels for the perception of form, color, movement, and depth , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  B. Richmond,et al.  Implantation of magnetic search coils for measurement of eye position: An improved method , 1980, Vision Research.

[18]  John H. R. Maunsell,et al.  Functions of the ON and OFF channels of the visual system , 1986, Nature.

[19]  T. Wiesel,et al.  The influence of contextual stimuli on the orientation selectivity of cells in primary visual cortex of the cat , 1990, Vision Research.

[20]  M. Posner,et al.  Orienting of Attention* , 1980, The Quarterly journal of experimental psychology.

[21]  T D Albright,et al.  Segmentation by Color Influences Responses of Motion-Sensitive Neurons in the Cortical Middle Temporal Visual Area , 1999, The Journal of Neuroscience.

[22]  R. Desimone,et al.  Local precision of visuotopic organization in the middle temporal area (MT) of the macaque , 2004, Experimental Brain Research.

[23]  J. Allman,et al.  Stimulus specific responses from beyond the classical receptive field: neurophysiological mechanisms for local-global comparisons in visual neurons. , 1985, Annual review of neuroscience.

[24]  J. Nelson,et al.  Orientation-selective inhibition from beyond the classic visual receptive field , 1978, Brain Research.

[25]  Khanh Nguyen,et al.  Use of a raster framebuffer in vision research , 1986 .

[26]  W. A. V. Grind,et al.  Integration and segregation of local motion signals: the role of contrast polarity , 1999, Vision Research.

[27]  C. Gilbert,et al.  Improvement in visual sensitivity by changes in local context: Parallel studies in human observers and in V1 of alert monkeys , 1995, Neuron.

[28]  D. Hubel,et al.  Receptive fields and functional architecture of monkey striate cortex , 1968, The Journal of physiology.

[29]  C. Wehrhahn,et al.  Detection facilitation by collinear stimuli in humans: Dependence on strength and sign of contrast , 1998, Vision Research.

[30]  T D Albright,et al.  What happens if it changes color when it moves?: the nature of chromatic input to macaque visual area MT , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  Peter H. Schiller,et al.  The connections of the retinal on and off pathways to the lateral geniculate nucleus of the monkey , 1984, Vision Research.

[32]  Victor A. F. Lamme,et al.  Feedforward, horizontal, and feedback processing in the visual cortex , 1998, Current Opinion in Neurobiology.

[33]  T. Albright,et al.  Contextual influences on visual processing. , 2002, Annual review of neuroscience.

[34]  K. Albus,et al.  Effects of interacting visual patterns on single cell responses in cat's striate cortex , 1977, Vision Research.

[35]  J. B. Levitt,et al.  Contrast dependence of contextual effects in primate visual cortex , 1997, nature.

[36]  D. Foster,et al.  Orientation contrast vs orientation in line-target detection , 1995, Vision Research.

[37]  T. Wiesel,et al.  Targets of horizontal connections in macaque primary visual cortex , 1991, The Journal of comparative neurology.

[38]  J. Movshon,et al.  Time Course and Time-Distance Relationships for Surround Suppression in Macaque V1 Neurons , 2003, The Journal of Neuroscience.

[39]  S P McKee,et al.  Interference with line-orientation sensitivity. , 1976, Journal of the Optical Society of America.

[40]  Jean Bennett,et al.  Lateral Connectivity and Contextual Interactions in Macaque Primary Visual Cortex , 2002, Neuron.

[41]  A. Grinvald,et al.  Relationship between intrinsic connections and functional architecture revealed by optical imaging and in vivo targeted biocytin injections in primate striate cortex. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[42]  D. Hubel,et al.  Uniformity of monkey striate cortex: A parallel relationship between field size, scatter, and magnification factor , 1974, The Journal of comparative neurology.

[43]  Victor A. F. Lamme The neurophysiology of figure-ground segregation in primary visual cortex , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  C. Blakemore,et al.  Lateral inhibition between orientation detectors in the cat's visual cortex , 2004, Experimental Brain Research.

[45]  J. Movshon,et al.  Nature and interaction of signals from the receptive field center and surround in macaque V1 neurons. , 2002, Journal of neurophysiology.

[46]  R. Shapley,et al.  Visual spatial characterization of macaque V1 neurons. , 2001, Journal of neurophysiology.

[47]  Jay Hegdé,et al.  How Selective Are V1 Cells for Pop-Out Stimuli? , 2003, The Journal of Neuroscience.

[48]  D. V. van Essen,et al.  Neuronal responses to static texture patterns in area V1 of the alert macaque monkey. , 1992, Journal of neurophysiology.

[49]  DH Hubel,et al.  Color and contrast sensitivity in the lateral geniculate body and primary visual cortex of the macaque monkey , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  U. Eysel,et al.  Orientation-specific relationship between populations of excitatory and inhibitory lateral connections in the visual cortex of the cat. , 1997, Cerebral cortex.

[51]  D. Fitzpatrick,et al.  Orientation Selectivity and the Arrangement of Horizontal Connections in Tree Shrew Striate Cortex , 1997, The Journal of Neuroscience.

[52]  C Wehrhahn,et al.  Contextual influence on orientation discrimination of humans and responses of neurons in V1 of alert monkeys. , 2000, Journal of neurophysiology.

[53]  C. Gilbert,et al.  Topography of contextual modulations mediated by short-range interactions in primary visual cortex , 1999, Nature.

[54]  T. Albright,et al.  Image Segmentation Enhances Discrimination of Motion in Visual Noise , 1997, Vision Research.

[55]  I. Ohzawa,et al.  Length and width tuning of neurons in the cat's primary visual cortex. , 1994, Journal of neurophysiology.

[56]  T D Albright,et al.  Form-cue invariant motion processing in primate visual cortex. , 1992, Science.

[57]  Salvatore Squatrito,et al.  Influences of uniform and textured backgrounds on the impulse activity of neurons in area V1 of the alert macaque , 1990, Brain Research.

[58]  D. Hubel,et al.  Spatial and chromatic interactions in the lateral geniculate body of the rhesus monkey. , 1966, Journal of neurophysiology.

[59]  Victor A. F. Lamme,et al.  Contextual Modulation in Primary Visual Cortex , 1996, The Journal of Neuroscience.

[60]  L. Maffei,et al.  The unresponsive regions of visual cortical receptive fields , 1976, Vision Research.

[61]  C. Blakemore,et al.  The neural mechanism of binocular depth discrimination , 1967, The Journal of physiology.

[62]  T. Albright,et al.  Image Segmentation Cues in Motion Processing: Implications for Modularity in Vision , 1993, Journal of Cognitive Neuroscience.

[63]  J. Movshon,et al.  A computational analysis of the relationship between neuronal and behavioral responses to visual motion , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[64]  R. Desimone,et al.  Selective attention gates visual processing in the extrastriate cortex. , 1985, Science.

[65]  G. Caputo,et al.  The Role of the Background: Texture Segregation and Figure—Ground Segmentation , 1996, Vision Research.