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  • Review Article
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Cognitive neuroscience

Primary visual cortex and visual awareness

Key Points

  • There are two main theories that pertain to the role of the primary visual cortex (V1) in visual awareness. Hierarchical models propose that although V1 provides necessary input, only high-level extrastriate areas that project to frontal-parietal attentional areas are directly involved in awareness. Interactive models propose that dynamic recurrent circuits between V1 and higher areas are necessary to maintain a visual representation in awareness. These models yield different predictions about whether awareness will be impaired by V1 disruption if extrastriate activity remains intact.

  • V1 damage severely impairs visual awareness, indicating that this region is necessary for normal conscious vision. Lesions to extrastriate areas lead to more specific visual deficits, whereas damage to parietal and/or superior-temporal areas can lead to gross visual neglect of contralateral space. Therefore, no single brain area is sufficient for visual awareness. Nonetheless, V1 seems to be the only single cortical area that is crucial for visual awareness.

  • Some subjects with V1 lesions can make accurate forced-choice visual discriminations in the absence of reported awareness. These implicit residual abilities (blindsight) presumably reflect the sustained activity that is found in many extrastriate areas, including motion-sensitive areas MT and V3A, and object-sensitive areas V4/V8 and the lateral occipital area. Similarly, motion phosphenes elicited by transcranial magnetic stimulation of area MT can be disrupted by subsequent stimulation to V1, indicating that extrastriate activity alone might be insufficient for awareness and that feedback projections from MT to V1 may be important for awareness of motion.

  • V1 activity is strongly associated with awareness under certain ambiguous perceptual conditions. During binocular rivalry, awareness spontaneously alternates between two competing monocular images. Human neuroimaging studies have revealed strong awareness-related modulations in V1 during rivalry. Likewise, neurophysiological and functional magnetic resonance imaging studies of visual detection tasks have found that V1 activity is greater for perceived than unperceived targets, and that the degree of response enhancement can predict detection performance.

  • However, not all studies have found a consistent relationship between V1 activity and awareness, including those of internally generated visual experiences (such as hallucinations, dreaming or imagery). In some studies, changes in perception are associated with increased extrastriate activity and concomitant decreases in V1 activity, indicating a more complex relationship.

  • Current evidence indicates that V1 activity is necessary for normal conscious perception and is closely associated with some forms of visual awareness. Further investigation of V1 and its interactions with higher areas might provide important insights into the neural basis of visual awareness.

Abstract

The primary visual cortex (V1) is probably the best characterized area of primate cortex, but whether this region contributes directly to conscious visual experience is controversial. Early neurophysiological and neuroimaging studies found that visual awareness was best correlated with neural activity in extrastriate visual areas, but recent studies have found similarly powerful effects in V1. Lesion and inactivation studies have provided further evidence that V1 might be necessary for conscious perception. Whereas hierarchical models propose that damage to V1 simply disrupts the flow of information to extrastriate areas that are crucial for awareness, interactive models propose that recurrent connections between V1 and higher areas form functional circuits that support awareness. Further investigation into V1 and its interactions with higher areas might uncover fundamental aspects of the neural basis of visual awareness.

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Figure 1: Connections between a subset of cortical visual areas (schematic diagram).
Figure 2: Extrastriate activations to objects in the absence of primary visual cortex (V1) and reported awareness.
Figure 3: Functional magnetic resonance imaging correlates of binocular rivalry in human primary visual cortex.
Figure 4: Multi-unit activity in primary visual cortex correlates with conscious detection of visual figures on a background.
Figure 5: Relationship between timing of primary visual cortex disruption and visual awareness.

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References

  1. Felleman, D. J. & Van Essen, D. C. Distributed hierarchical processing in the primate cerebral cortex. Cereb. Cortex 1, 1–47 (1991).

    CAS  PubMed  Google Scholar 

  2. Cowey, A. & Stoerig, P. The neurobiology of blindsight. Trends Neurosci. 14, 140–145 (1991).

    CAS  PubMed  Google Scholar 

  3. Salin, P. A. & Bullier, J. Corticocortical connections in the visual system: structure and function. Physiol. Rev. 75, 107–154 (1995).

    CAS  PubMed  Google Scholar 

  4. Falchier, A., Clavagnier, S., Barone, P. & Kennedy, H. Anatomical evidence of multimodal integration in primate striate cortex. J. Neurosci. 22, 5749–5759 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Barone, P., Batardiere, A., Knoblauch, K. & Kennedy, H. Laminar distribution of neurons in extrastriate areas projecting to visual areas V1 and V4 correlates with the hierarchical rank and indicates the operation of a distance rule. J. Neurosci. 20, 3263–3281 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  6. Barlow, H. B., Blakemore, C. & Pettigrew, J. D. The neural mechanism of binocular depth discrimination. J. Physiol. (Lond.) 193, 327–342 (1967).

    CAS  Google Scholar 

  7. Cumming, B. G. An unexpected specialization for horizontal disparity in primate primary visual cortex. Nature 418, 633–636 (2002).

    CAS  PubMed  Google Scholar 

  8. Hubel, D. H. & Wiesel, T. N. Receptive fields, binocular interaction, and functional architecture in the cat's visual cortex. J. Physiol. (Lond.) 160, 106–154 (1962).

    CAS  Google Scholar 

  9. Hubel, D. H. & Wiesel, T. N. Receptive fields and functional architecture of monkey striate cortex. J. Physiol. (Lond.) 195, 215–243 (1968).

    Article  CAS  Google Scholar 

  10. De Valois, K. K., De Valois, R. L. & Yund, E. W. Responses of striate cortex cells to grating and checkerboard patterns. J. Physiol. (Lond.) 291, 483–505 (1979).

    CAS  Google Scholar 

  11. Ungerleider, L. G. & Mishkin, M. in Analysis of Visual Behavior (eds Ingle, D. J., Goodale, M. A. & Mansfield, R. J. W.) 549–586 (MIT Press, Cambridge, Massachusetts, 1982).

    Google Scholar 

  12. Inouye, T. Visual Disturbances following Gunshot Wounds of the Cortical Visual Area (translated by M. Glickestein & M. Fahle) (Oxford Univ. Press, Oxford, 2000; Brain 123, Suppl. 1–101).

    Google Scholar 

  13. Holmes, G. Disturbances of vision by cerebral lesions. Brit. J. Ophthalmol. 2, 353–384 (1918).

    CAS  Google Scholar 

  14. Rees, G., Kreiman, G. & Koch, C. Neural correlates of consciousness in humans. Nature Rev. Neurosci. 3, 261–270 (2002).

    CAS  Google Scholar 

  15. Crick, F. & Koch, C. Are we aware of neural activity in primary visual cortex? Nature 375, 121–123 (1995).

    CAS  PubMed  Google Scholar 

  16. Zeki, S. Localization and globalization in conscious vision. Annu. Rev. Neurosci. 24, 57–86 (2001).

    CAS  PubMed  Google Scholar 

  17. Zeki, S. M. Functional organization of a visual area in the posterior bank of the superior temporal sulcus of the rhesus monkey. J. Physiol. (Lond.) 236, 549–573 (1974).

    CAS  Google Scholar 

  18. Zeki, S. M. Colour coding in the superior temporal sulcus of rhesus monkey visual cortex. Proc. R. Soc. Lond. B 197, 195–223 (1977).

    CAS  PubMed  Google Scholar 

  19. Gross, C. G., Bender, D. B. & Rocha-Miranda, C. E. Visual receptive fields of neurons in inferotemporal cortex of the monkey. Science 166, 1303–1306 (1969).

    CAS  PubMed  Google Scholar 

  20. Leopold, D. A. & Logothetis, N. K. Multistable phenomena: changing views in perception. Trends Cogn. Sci. 3, 254–264 (1999).

    CAS  PubMed  Google Scholar 

  21. Pollen, D. A. On the neural correlates of visual perception. Cereb. Cortex 9, 4–19 (1999).

    CAS  PubMed  Google Scholar 

  22. Lamme, V. A. & Roelfsema, P. R. The distinct modes of vision offered by feedforward and recurrent processing. Trends Neurosci. 23, 571–579 (2000).

    CAS  PubMed  Google Scholar 

  23. Bullier, J. Integrated model of visual processing. Brain Res. Brain Res. Rev. 36, 96–107 (2001).

    CAS  PubMed  Google Scholar 

  24. Treisman, A. M. & Gelade, G. A feature-integration theory of attention. Cogn. Psychol. 12, 97–136 (1980).

    CAS  PubMed  Google Scholar 

  25. Baars, B. J. In the Theater of Consciousness: the Workspace of the Mind (Oxford Univ. Press, New York, 1996).

    Google Scholar 

  26. Engel, A. K. & Singer, W. Temporal binding and the neural correlates of sensory awareness. Trends Cogn. Sci. 5, 16–25 (2001).

    PubMed  Google Scholar 

  27. Tononi, G. & Edelman, G. M. Consciousness and complexity. Science 282, 1846–1851 (1998).

    CAS  PubMed  Google Scholar 

  28. Weiskrantz, L. Blindsight: a Case Study in its Implications (Oxford Univ. Press, Oxford, 1986). A widely cited book that details the discovery and first investigations of blindsight or vision without awareness.

    Google Scholar 

  29. Stoerig, P. & Cowey, A. Wavelength discrimination in blindsight. Brain 115, 425–444 (1992).

    PubMed  Google Scholar 

  30. Stoerig, P. & Barth, E. Low-level phenomenal vision despite unilateral destruction of primary visual cortex. Conscious. Cogn. 10, 574–587 (2001).

    CAS  PubMed  Google Scholar 

  31. Stoerig, P. & Cowey, A. Blindsight in man and monkey. Brain 120, 535–559 (1997).

    PubMed  Google Scholar 

  32. Stoerig, P., Zontanou, A. & Cowey, A. Aware or unaware: assessment of cortical blindness in four men and a monkey. Cereb. Cortex 12, 565–574 (2002).

    PubMed  Google Scholar 

  33. Cowey, A. & Stoerig, P. Blindsight in monkeys. Nature 373, 247–249 (1995). A compelling behavioural demonstration that monkeys with striate lesions lack awareness for items they can discriminate under forced-choice conditions.

    CAS  PubMed  Google Scholar 

  34. Azzopardi, P. & Cowey, A. Blindsight and visual awareness. Conscious. Cogn. 7, 292–311 (1998).

    CAS  PubMed  Google Scholar 

  35. Barbur, J. L., Watson, J. D., Frackowiak, R. S. & Zeki, S. Conscious visual perception without V1. Brain 116, 1293–1302 (1993).

    PubMed  Google Scholar 

  36. Riddoch, G. Dissociation of visual perceptions due to occipital injuries, with especial reference to appreciation of movement. Brain 40, 15–57 (1917).

    Google Scholar 

  37. Weiskrantz, L., Cowey, A. & Hodinott-Hill, I. Prime-sight in a blindsight subject. Nature Neurosci. 5, 101–102 (2002).

    CAS  PubMed  Google Scholar 

  38. Faubert, J., Diaconu, V., Ptito, M. & Ptito, A. Residual vision in the blind field of hemidecorticated humans predicted by a diffusion scatter model and selective spectral absorption of the human eye. Vision Res. 39, 149–157 (1999).

    CAS  PubMed  Google Scholar 

  39. Girard, P., Salin, P. A. & Bullier, J. Visual activity in areas V3a and V3 during reversible inactivation of area V1 in the macaque monkey. J. Neurophysiol. 66, 1493–1503 (1991).

    CAS  PubMed  Google Scholar 

  40. Rodman, H. R., Gross, C. G. & Albright, T. D. Afferent basis of visual response properties in area MT of the macaque. I. Effects of striate cortex removal. J. Neurosci. 9, 2033–2050 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  41. Moore, T., Rodman, H. R., Repp, A. B. & Gross, C. G. Localization of visual stimuli after striate cortex damage in monkeys: parallels with human blindsight. Proc. Natl Acad. Sci. USA 92, 8215–8218 (1995).

    CAS  PubMed  PubMed Central  Google Scholar 

  42. Goebel, R., Muckli, L., Zanella, F. E., Singer, W. & Stoerig, P. Sustained extrastriate cortical activation without visual awareness revealed by fMRI studies of hemianopic patients. Vision Res. 41, 1459–1474 (2001).

    CAS  PubMed  Google Scholar 

  43. Merigan, W. H., Nealey, T. A. & Maunsell, J. H. Visual effects of lesions of cortical area V2 in macaques. J. Neurosci. 13, 3180–3191 (1993).

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Zihl, J., von Cramon, D., Mai, N. & Schmid, C. Disturbance of movement vision after bilateral posterior brain damage. Further evidence and follow up observations. Brain 114, 2235–2252 (1991).

    PubMed  Google Scholar 

  45. Zihl, J., von Cramon, D. & Mai, N. Selective disturbance of movement vision after bilateral brain damage. Brain 106, 313–340 (1983).

    PubMed  Google Scholar 

  46. Plant, G. T., Laxer, K. D., Barbaro, N. M., Schiffman, J. S. & Nakayama, K. Impaired visual motion perception in the contralateral hemifield following unilateral posterior cerebral lesions in humans. Brain 116, 1303–1335 (1993).

    PubMed  Google Scholar 

  47. Pasternak, T. & Merigan, W. H. Motion perception following lesions of the superior temporal sulcus in the monkey. Cereb. Cortex 4, 247–259 (1994).

    CAS  PubMed  Google Scholar 

  48. Meadows, J. C. Disturbed perception of colours associated with localized cerebral lesions. Brain 97, 615–632 (1974).

    CAS  PubMed  Google Scholar 

  49. Zeki, S. A century of cerebral achromatopsia. Brain 113, 1721–1777 (1990).

    PubMed  Google Scholar 

  50. Wade, A. R., Brewer, A. A., Rieger, J. W. & Wandell, B. A. Functional measurements of human ventral occipital cortex: retinotopy and colour. Phil. Trans. R. Soc. Lond. B 357, 963–973 (2002). | PubMed

    Google Scholar 

  51. Hadjikhani, N., Liu, A. K., Dale, A. M., Cavanagh, P. & Tootell, R. B. Retinotopy and color sensitivity in human visual cortical area V8. Nature Neurosci. 1, 235–241 (1998).

    CAS  PubMed  Google Scholar 

  52. Heywood, C. & Cowey, A. With color in mind. Nature Neurosci. 1, 171–173 (1998).

    CAS  PubMed  Google Scholar 

  53. Gross, C. G. How inferior temporal cortex became a visual area. Cereb. Cortex 5, 455–469 (1994).

    Google Scholar 

  54. Meadows, J. C. The anatomical basis of prosopagnosia. J. Neurol. Neurosurg. Psychiatry 37, 489–501 (1974).

    CAS  PubMed  PubMed Central  Google Scholar 

  55. Vallar, G. & Perani, D. The anatomy of unilateral neglect after right-hemisphere stroke lesions. A clinical/CT-scan correlation study in man. Neuropsychologia 24, 609–622 (1986).

    CAS  PubMed  Google Scholar 

  56. Karnath, H. O., Ferber, S. & Himmelbach, M. Spatial awareness is a function of the temporal not the posterior parietal lobe. Nature 411, 950–953 (2001).

    CAS  PubMed  Google Scholar 

  57. Balint, R. Psychic paralysis of gaze, optic ataxia, and spatial disorder of attention. Cogn. Neuropsychol. 12, 265–281 (1995).

    Google Scholar 

  58. Andersen, R. A. & Buneo, C. A. Intentional maps in posterior parietal cortex. Annu. Rev. Neurosci. 25, 189–220 (2002).

    CAS  PubMed  Google Scholar 

  59. Watson, R. T., Valenstein, E., Day, A. & Heilman, K. M. Posterior neocortical systems subserving awareness and neglect. Neglect associated with superior temporal sulcus but not area 7 lesions. Arch. Neurol. 51, 1014–1021 (1994).

    CAS  PubMed  Google Scholar 

  60. Blake, R. & Logothetis, N. K. Visual competition. Nature Rev. Neurosci. 3, 13–21 (2002).

    CAS  Google Scholar 

  61. Wheatstone, C. Contributions to the physiology of vision. Part I. On some remarkable, and hitherto unobserved, phenomena of binocular vision. Phil. Trans. R. Soc. Lond. B 128, 371–394 (1838)

    Google Scholar 

  62. Lansing, R. W. Electroencephalographic correlates of binocular rivalry in man. Science 146, 1325–1327 (1964). The first study to identify a neural correlate of awareness during binocular rivalry by using EEG to measure occipital responses.

    CAS  PubMed  Google Scholar 

  63. Cobb, W. A., Morton, H. B. & Ettlinger, G. Cerebral potential evoked by pattern reversal and their suppression in visual rivalry. Nature 216, 1123–1125 (1967).

    CAS  PubMed  Google Scholar 

  64. Logothetis, N. K. & Schall, J. D. Neuronal correlates of subjective visual perception. Science 245, 761–763 (1989). The first of a series of influential studies recording single-unit activity in monkeys that reported their perceptions during rivalry (see also references 65 and 66).

    CAS  PubMed  Google Scholar 

  65. Leopold, D. A. & Logothetis, N. K. Activity changes in early visual cortex reflect monkeys' percepts during binocular rivalry. Nature 379, 549–553 (1996).

    CAS  PubMed  Google Scholar 

  66. Sheinberg, D. L. & Logothetis, N. K. The role of temporal cortical areas in perceptual organization. Proc. Natl Acad. Sci. USA 94, 3408–3413 (1997).

    CAS  PubMed  PubMed Central  Google Scholar 

  67. Blake, R. A neural theory of binocular rivalry. Psychol. Rev. 96, 145–167 (1989).

    CAS  PubMed  Google Scholar 

  68. Tong, F. & Engel, S. A. Interocular rivalry revealed in the human cortical blind-spot representation. Nature 411, 195–199 (2001).

    CAS  PubMed  Google Scholar 

  69. Polonsky, A., Blake, R., Braun, J. & Heeger, D. J. Neuronal activity in human primary visual cortex correlates with perception during binocular rivalry. Nature Neurosci. 3, 1153–1159 (2000).

    CAS  PubMed  Google Scholar 

  70. Tong, F. Competing theories of binocular rivalry: a possible resolution. Brain Mind 2, 55–83 (2001).

    Google Scholar 

  71. Tong, F., Nakayama, K., Vaughan, J. T. & Kanwisher, N. Binocular rivalry and visual awareness in human extrastriate cortex. Neuron 21, 753–759 (1998). The first fMRI study to demonstrate a tight coupling between cortical activity and the contents of human visual awareness during rivalry (see also references 68, 69 and 72).

    CAS  PubMed  Google Scholar 

  72. Lumer, E. D., Friston, K. J. & Rees, G. Neural correlates of perceptual rivalry in the human brain. Science 280, 1930–1934 (1998).

    CAS  PubMed  Google Scholar 

  73. Zipser, K., Lamme, V. A. & Schiller, P. H. Contextual modulation in primary visual cortex. J. Neurosci. 16, 7376–7389 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  74. Rossi, A. F., Desimone, R. & Ungerleider, L. G. Contextual modulation in primary visual cortex of macaques. J. Neurosci. 21, 1698–1709 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  75. Super, H., Spekreijse, H. & Lamme, V. A. Two distinct modes of sensory processing observed in monkey primary visual cortex (V1). Nature Neurosci. 4, 304–310 (2001).

    CAS  PubMed  Google Scholar 

  76. Lee, T. S., Yang, C. F., Romero, R. D. & Mumford, D. Neural activity in early visual cortex reflects behavioral experience and higher-order perceptual saliency. Nature Neurosci. 5, 589–597 (2002). A single-unit study showing that V1 activity in the monkey reflects the perceptual salience of a target during visual search and can predict performance accuracy.

    CAS  PubMed  Google Scholar 

  77. Ress, D., Nadell, D. E. & Heeger, D. J. Neural correlates of threshold visual pattern detection. Soc. Neurosci. Abstr. 783.7 (2001).

  78. Ress, D., Backus, B. T. & Heeger, D. J. Activity in primary visual cortex predicts performance in a visual detection task. Nature Neurosci. 3, 940–945 (2000). An elegant fMRI study showing that attentional modulation levels in V1 can predict near-threshold detection performance.

    CAS  PubMed  Google Scholar 

  79. Grunewald, A., Bradley, D. C. & Andersen, R. A. Neural correlates of structure-from-motion perception in macaque V1 and MT. J. Neurosci. 22, 6195–6207 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  80. Sterzer, P., Russ, M. O., Preibisch, C. & Kleinschmidt, A. Neural correlates of spontaneous direction reversals in ambiguous apparent visual motion. Neuroimage 15, 908–916 (2002).

    PubMed  Google Scholar 

  81. Muckli, L. et al. Apparent motion: event-related functional magnetic resonance imaging of perceptual switches and states. J. Neurosci. 22, RC219 (2002).

    PubMed  PubMed Central  Google Scholar 

  82. Murray, S. O., Kersten, D., Olshausen, B. A., Schrater, P. & Woods, D. L. Shape perception reduces activity in human primary visual cortex. Proc. Natl Acad. Sci. USA 99, 15164–15169 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  83. Kleinschmidt, A., Buchel, C., Zeki, S. & Frackowiak, R. S. Human brain activity during spontaneously reversing perception of ambiguous figures. Proc. R. Soc. Lond. B 265, 2427–2433 (1998).

    CAS  Google Scholar 

  84. Schoups, A., Vogels, R., Qian, N. & Orban, G. Practising orientation identification improves orientation coding in V1 neurons. Nature 412, 549–553 (2001).

    CAS  PubMed  Google Scholar 

  85. Rossi, A. F. & Paradiso, M. A. Neural correlates of perceived brightness in the retina, lateral geniculate nucleus, and striate cortex. J. Neurosci. 19, 6145–6156 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  86. Kapadia, M. K., Westheimer, G. & Gilbert, C. D. Spatial distribution of contextual interactions in primary visual cortex and in visual perception. J. Neurophysiol. 84, 2048–2062 (2000).

    CAS  PubMed  Google Scholar 

  87. Sugita, Y. Grouping of image fragments in primary visual cortex. Nature 401, 269–272 (1999).

    CAS  PubMed  Google Scholar 

  88. von der Heydt, R., Peterhans, E. & Baumgartner, G. Illusory contours and cortical neuron responses. Science 224, 1260–1262 (1984).

    CAS  PubMed  Google Scholar 

  89. Grosof, D. H., Shapley, R. M. & Hawken, M. J. Macaque V1 neurons can signal 'illusory' contours. Nature 365, 550–552 (1993).

    CAS  PubMed  Google Scholar 

  90. Fiorani, M., Rosa, M. G. P., Gattass, R. & Rocha-Miranda, C. E. Dynamic surrounds of receptive fields in primate striate cortex: a physiological basis for perceptual completion? Neurobiology 89, 8547–8551 (1992). | PubMed |

    Google Scholar 

  91. Gilbert, C. D. & Wiesel, T. N. Receptive field dynamics in adult primary visual cortex. Nature 356, 150–152 (1992).

    CAS  PubMed  Google Scholar 

  92. de Weerd, P., Gattass, R., Desimone, R. & Ungerleider, L. G. Responses of cells in monkey visual cortex during perceptual filling-in of an artificial scotoma. Nature 377, 731–734 (1995).

    CAS  PubMed  Google Scholar 

  93. Hammond, P., Mouat, G. S. & Smith, A. T. Motion after-effects in cat striate cortex elicited by moving gratings. Exp. Brain Res. 60, 411–416 (1985).

    CAS  PubMed  Google Scholar 

  94. Dragoi, V., Rivadulla, C. & Sur, M. Foci of orientation plasticity in visual cortex. Nature 411, 80–86 (2001).

    CAS  PubMed  Google Scholar 

  95. Engel, S. A. & Furmanski, C. S. Selective adaptation to color contrast in human primary visual cortex. J. Neurosci. 21, 3949–3954 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  96. Sengpiel, F. & Blakemore, C. Interocular control of neuronal responsiveness in cat visual cortex. Nature 368, 847–850 (1994).

    CAS  PubMed  Google Scholar 

  97. Macknik, S. L. & Livingstone, M. S. Neuronal correlates of visibility and invisibility in the primate visual system. Nature Neurosci. 1, 144–149 (1998).

    CAS  PubMed  Google Scholar 

  98. Schiller, P. H. Single unit analysis of backward visual masking and metacontrast in the cat lateral geniculate nucleus. Vision Res. 8, 855–866 (1968).

    CAS  PubMed  Google Scholar 

  99. Gur, M. & Snodderly, D. M. A dissociation between brain activity and perception: chromatically opponent cortical neurons signal chromatic flicker that is not perceived. Vision Res. 37, 377–382 (1997).

    CAS  PubMed  Google Scholar 

  100. He, S. & MacLeod, D. I. Orientation-selective adaptation and tilt after-effect from invisible patterns. Nature 411, 473–476 (2001). An original psychophysical study showing orientation-specific adaptation for high spatial frequency gratings that are too fine to be perceived, indicating that some amount of V1 processing can occur without awareness.

    CAS  PubMed  Google Scholar 

  101. Blake, R. & Fox, R. Adaptation to invisible gratings and the site of binocular rivalry suppression. Nature 249, 488–490 (1974).

    CAS  PubMed  Google Scholar 

  102. Nakamura, R. K. & Mishkin, M. Chronic 'blindness' following lesions of nonvisual cortex in the monkey. Exp. Brain Res. 63, 173–184 (1984).

    Google Scholar 

  103. Rees, G. et al. Unconscious activation of visual cortex in the damaged right hemisphere of a parietal patient with extinction. Brain 123, 1624–1633 (2000).

    PubMed  Google Scholar 

  104. Vuilleumier, P. et al. Neural fate of seen and unseen faces in visuospatial neglect: a combined event-related functional MRI and event-related potential study. Proc. Natl Acad. Sci. USA 98, 3495–3500 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  105. Dehaene, S. et al. Cerebral mechanisms of word masking and unconscious repetition priming. Nature Neurosci. 4, 752–758 (2001).

    CAS  PubMed  Google Scholar 

  106. Beck, D. M., Rees, G., Frith, C. D. & Lavie, N. Neural correlates of change detection and change blindness. Nature Neurosci. 4, 645–650 (2001).

    CAS  PubMed  Google Scholar 

  107. Ffytche, D. H. et al. The anatomy of conscious vision: an fMRI study of visual hallucinations. Nature Neurosci. 1, 738–742 (1998).

    CAS  PubMed  Google Scholar 

  108. Braun, A. R. et al. Dissociated pattern of activity in visual cortices and their projections during human rapid eye movement sleep. Science 279, 91–95 (1998).

    CAS  PubMed  Google Scholar 

  109. Hadjikhani, N. et al. Mechanisms of migraine aura revealed by functional MRI in human visual cortex. Proc. Natl Acad. Sci. USA 98, 4687–4692 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  110. Nunn, J. A. et al. Functional magnetic resonance imaging of synesthesia: activation of V4/V8 by spoken words. Nature Neurosci. 5, 371–375 (2002).

    CAS  PubMed  Google Scholar 

  111. Aleman, A., Rutten, G. J., Sitskoorn, M. M., Dautzenberg, G. & Ramsey, N. F. Activation of striate cortex in the absence of visual stimulation: an fMRI study of synesthesia. Neuroreport 12, 2827–2830 (2001).

    CAS  PubMed  Google Scholar 

  112. Kosslyn, S. M., Ganis, G. & Thompson, W. L. Neural foundations of imagery. Nature Rev. Neurosci. 2, 635–642 (2001).

    CAS  Google Scholar 

  113. Foerster, O. Beiträge zur Pathophysiologie der Sehbahn und der Sehsphäre. J. Psychol. Neurol. 39, 463–485 (1929).

    Google Scholar 

  114. Dobelle, W. H. & Mladejovsky, M. G. Phosphenes produced by electrical stimulation of human occipital cortex, and their application to the development of a prosthesis for the blind. J. Physiol. (Lond.) 243, 553–576 (1974).

    CAS  Google Scholar 

  115. Brindley, G. S. & Lewin, W. S. The sensations produced by electrical stimulation of the visual cortex. J. Physiol. (Lond.) 196, 479–493 (1968).

    CAS  Google Scholar 

  116. Salzman, C. D., Britten, K. H. & Newsome, W. T. Cortical microstimulation influences perceptual judgements of motion direction. Nature 346, 174–177 (1990). A classic study showing that a monkey's perceptual interpretation of ambiguous motion can be biased by electrical stimulation in area MT.

    CAS  PubMed  Google Scholar 

  117. Cowey, A. & Walsh, V. Magnetically induced phosphenes in sighted, blind and blindsighted observers. Neuroreport 11, 3269–3273 (2000).

    CAS  PubMed  Google Scholar 

  118. Girard, P., Hupe, J. M. & Bullier, J. Feedforward and feedback connections between areas V1 and V2 of the monkey have similar rapid conduction velocities. J. Neurophysiol. 85, 1328–1331 (2001).

    CAS  PubMed  Google Scholar 

  119. Movshon, J. A. & Newsome, W. T. Visual response properties of striate cortical neurons projecting to area MT in macaque monkeys. J. Neurosci. 16, 7733–7741 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  120. Penfield, W. The Cerebral Cortex of Man: a Clinical Study of Localization of Function (Macmillan, New York, 1950).

    Google Scholar 

  121. Amassian, V. E. et al. Suppression of visual perception by magnetic coil stimulation of human occipital cortex. Electroencephalogr. Clin. Neurophysiol. 74, 458–462 (1989).

    CAS  PubMed  Google Scholar 

  122. Kamitani, Y. & Shimojo, S. Manifestation of scotomas created by transcranial magnetic stimulation of human visual cortex. Nature Neurosci. 2, 767–771 (1999).

    CAS  PubMed  Google Scholar 

  123. Corthout, E., Uttl, B., Walsh, V., Hallett, M. & Cowey, A. Timing of activity in early visual cortex as revealed by transcranial magnetic stimulation. Neuroreport 10, 2631–2634 (1999).

    CAS  PubMed  Google Scholar 

  124. Beckers, G. & Homberg, V. Cerebral visual motion blindness: transitory akinetopsia induced by transcranial magnetic stimulation of human area V5. Proc. R. Soc. Lond. B 249, 173–178 (1992).

    CAS  Google Scholar 

  125. Pascual-Leone, A. & Walsh, V. Fast backprojections from the motion to the primary visual area necessary for visual awareness. Science 292, 510–512 (2001). An innovative TMS study that tested whether feedback projections from MT to V1 might be necessary for awareness of motion phosphenes.

    CAS  PubMed  Google Scholar 

  126. di Lollo, V., Enns, J. T. & Rensink, R. A. Competition for consciousness among visual events: the psychophysics of reentrant visual processes. J. Exp. Psychol. Gen. 129, 481–507 (2000). | PubMed

    CAS  PubMed  Google Scholar 

  127. Breitmeyer, B. G. Visual Masking: an Integrative Approach (Clarendon, Oxford, 1984).

    Google Scholar 

  128. Colombo, M., Colombo, A. & Gross, C. G. Bartolomeo Panizza's Observations on the optic nerve (1855). Brain Res. Bull. 58, 529–539 (2002).

    PubMed  Google Scholar 

  129. Ferrier, D. Functions of the Brain (Smith, Elder & Co., London, 1876).

    Google Scholar 

  130. Munk, H. translated in von Bonin, G. Some Papers on the Cerebral Cortex (Thomas, Springfield, Illinois, 1960).

    Google Scholar 

  131. Henschen, S. E. On the visual path and centre. Brain 16, 170–180 (1893).

    Google Scholar 

  132. He, S., Cavanagh, P. & Intriligator, J. Attentional resolution and the locus of visual awareness. Nature 383, 334–337 (1996).

    CAS  PubMed  Google Scholar 

  133. Motter, B. C. Focal attention produces spatially selective processing in visual cortical areas V1, V2, and V4 in the presence of competing stimuli. J. Neurophysiol. 70, 909–919 (1993).

    CAS  PubMed  Google Scholar 

  134. Moran, J. & Desimone, R. Selective attention gates visual processing in the extrastriate cortex. Science 229, 782–784 (1985).

    CAS  PubMed  Google Scholar 

  135. Vidyasagar, T. R. Gating of neuronal responses in macaque primary visual cortex by an attentional spotlight. Neuroreport 9, 1947–1952 (1998).

    CAS  PubMed  Google Scholar 

  136. Ito, M. & Gilbert, C. D. Attention modulates contextual influences in the primary visual cortex of alert monkeys. Neuron 22, 593–604 (1999).

    CAS  PubMed  Google Scholar 

  137. Roelsema, P. R., Lamme, V. A. & Spekreijse, H. Object-based attention in the primary visual cortex of the macaque monkey. Nature 395, 376–381 (1998). A compelling demonstration of object-based attention effects in V1 of the monkey.

    Google Scholar 

  138. Mehta, A. D., Ulbert, I. & Schroeder, C. E. Intermodal selective attention in monkeys. I: distribution and timing of effects across visual areas. Cereb. Cortex 10, 343–358 (2000).

    CAS  PubMed  Google Scholar 

  139. Watanabe, T. et al. Task-dependent influences of attention on the activation of human primary visual cortex. Proc. Natl Acad. Sci. USA 95, 11489–11492 (1998).

    CAS  PubMed  PubMed Central  Google Scholar 

  140. Gandhi, S. P., Heeger, D. J. & Boynton, G. M. Spatial attention affects brain activity in human primary visual cortex. Proc. Natl Acad. Sci. USA 96, 3314–3319 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  141. Brefczynski, J. A. & DeYoe, E. A. A physiological correlate of the 'spotlight' of visual attention. Nature Neurosci. 2, 370–374 (1999).

    CAS  PubMed  Google Scholar 

  142. Somers, D. C., Dale, A. M., Seiffert, A. E. & Tootell, R. B. Functional MRI reveals spatially specific attentional modulation in human primary visual cortex. Proc. Natl Acad. Sci. USA 96, 1663–1668 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  143. Saenz, M., Buracas, G. T. & Boynton, G. M. Global effects of feature-based attention in human visual cortex. Nature Neurosci. 5, 631–632 (2002).

    CAS  PubMed  Google Scholar 

  144. O'Connor, D. H., Fukui, M. M., Pinsk, M. A. & Kastner, S. Attention modulates responses in the human lateral geniculate nucleus. Nature Neurosci. 15, 1203–1209 (2002). | PubMed

    Google Scholar 

  145. Vanduffel, W., Tootell, R. B. & Orban, G. A. Attention-dependent suppression of metabolic activity in the early stages of the macaque visual system. Cereb. Cortex 10, 109–126 (2000).

    CAS  PubMed  Google Scholar 

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Acknowledgements

I would like to thank C. Gross, S. Kastner, T. Moore and A. Seiffert for helpful comments on this manuscript. This work was supported by the National Institutes of Health, James S. McDonnell Foundation and Pew Charitable Trusts.

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FURTHER INFORMATION

Encyclopedia of Life Sciences

brain imaging: localization of brain functions

brain imaging: observing ongoing neural activity

magnetic resonance imaging

MIT Encyclopedia of Cognitive Science

consciousness

magnetic resonance imaging

positron emission tomography

top–down processing in vision

Glossary

PRIMARY VISUAL CORTEX

The first cortical area to receive inputs from the eye via the geniculostriate pathway; also referred to as V1, area 17 and striate cortex.

EXTRASTRIATE CORTEX

A belt of visually responsive areas of cortex surrounding the primary visual cortex.

MT AND MST

Motion sensitive areas of extrastriate cortex.

PO AND PIP

The parieto-occipital (PO) and posterior intraparietal (PIP) visual areas lie in the dorsal stream and have weak reciprocal connections with V1. Their specific functions are not well understood.

FST

This visual area lies anterior to MT and MST in the floor of the superior temporal sulcus, and is also involved in motion perception but has not been extensively studied.

STP

The superior temporal polysensory area contains neurons that respond to visual, auditory and somatosensory stimuli, and responds strongly to visual motion.

TOE AND TE

These areas comprise the posterior and anterior portions of inferotemporal cortex (IT) respectively, and are involved in shape, object and face processing.

TH

This visual area lies in the parahippocampal gyrus, which has been implicated in scene perception and visual memory.

LIP

The lateral intraparietal area (LIP) is strongly implicated in visual-spatial attention and eye movement planning.

FRONTAL EYE FIELDS

(FEF). These areas are strongly implicated in visual–spatial attention and eye movement planning, and have strong connections with area LIP.

DORSAL STREAM

Visual brain areas that are involved in the localization of objects and are mostly found in the posterior/superior part of the brain.

VENTRAL STREAM

Visual brain areas that are involved in the identification of objects and are mostly found in the posterior/inferior part of the brain.

BACKWARD VISUAL MASKING

The reduced perception that occurs when a weak or brief stimulus is followed immediately by a stronger stimulus.

SYNAESTHESIA

An unusual 'mixing of the senses' in which a stimulus in one sensory modality (for example, a sound) elicits a percept in another modality (such as visual perception of a colour).

HEMIANOPIA

Loss of vision over half of the visual field, typically resulting from damage to the optic radiations that project to V1 or damage to V1 itself.

MOTION PHOSPHENES

Moving visual images that can be induced by stimulating parts of the visual system that are sensitive to motion.

ORTHODROMIC ACTIVATION

Activation of a target neuron by stimulation of an input neuron that synapses onto the target; action potentials are propagated in the normal direction along the input axon.

TRANSCRANIAL MAGNETIC STIMULATION

(TMS). A technique that is used to induce a transient interruption of normal activity in a relatively restricted area of the brain. It is based on the generation of a strong magnetic field near the area of interest, which, if changed rapidly enough, will induce an electric field that is sufficient to stimulate neurons.

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Tong, F. Primary visual cortex and visual awareness. Nat Rev Neurosci 4, 219–229 (2003). https://doi.org/10.1038/nrn1055

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