TL;DR: This target article uses as an example a form of reasoning about a function of “consciousness” based on the phenomenon of blindsight, where an obvious function of the machinery of accessconsciousness is illicitly transferred to phenomenal consciousness.
Abstract: Consciousness is a mongrel concept: there are a number of very different "consciousnesses." Phenomenal consciousness is experience; the phenomenally conscious aspect of a state is what it is like to be in that state. The mark of access-consciousness, by contrast, is availability for use in reasoning and rationally guiding speech and action. These concepts are often partly or totally conflated, with bad results. This target article uses as an example a form of reasoning about a function of "consciousness" based on the phenomenon of blindsight. Some information about stimuli in the blind field is represented in the brains of blindsight patients, as shown by their correct "guesses," but they cannot harness this information in the service of action, and this is said to show that a function of phenomenal consciousness is somehow to enable information represented in the brain to guide action. But stimuli in the blind field are BOTH access-unconscious and phenomenally unconscious. The fallacy is: an obvious function of the machinery of access-consciousness is illicitly transferred to phenomenal consciousness.
TL;DR: In this article, a form of reasoning about a function of consciousness based on the phenomenon of blindsight is presented, where it is shown that some information about stimuli in the blind field is represented in the brains of blind sight patients, as shown by their correct guesses.
Abstract: of the original article: Consciousness is a mongrel concept: there are a number of very different consciousnesses. Phenomenal consciousness is experience; the phenomenally conscious aspect of a state is what it is like to be in that state. The mark of access-consciousness, by contrast, is availability for use in reasoning and rationally guiding speech and action. These concepts are often partly or totally conflated, with bad results. This target article uses as an example a form of reasoning about a function of consciousness based on the phenomenon of blindsight. Some information about stimuli in the blind field is represented in the brains of blindsight patients, as shown by their correct guesses. They cannot harness this information in the service of action, however, and this is said to show that a function of phenomenal consciousness is somehow to enable information represented in the brain to guide action. But stimuli in the blind field are both access-unconscious and phenomenally unconscious. The fallacy is: an obvious function of the machinery of access-consciousness is illicitly transferred to phenomenal consciousness.
TL;DR: The increased activity in visual cortex in the absence of visual stimulation may reflect a top-down bias of neural signals in favor of the attended location, which derives from a fronto-parietal network.
TL;DR: 3. GazI zaniga, Residual vision in a scotoma: Implications for blindsight, Science, 258, 1489-1491 (1992).
Abstract: 3. R. Fendrich, CM. Wessinger, and M.S. GazI zaniga, Residual vision in a scotoma: Implications for blindsight, Science, 258, 1489-1491 (1992). 4. J.L. Barbur, J.D.G. Watson, R.S.j. Frackow iak, and S. Zeki, Conscious visual perception with out V1, Brain, 116, 1293 (1993). 5. A. Cowey and P. Stoerig, The neurobiology of blindsight, Trends in Neurosciences, 14, 140 (1991). 6. H.T. Rodman, CG. Gross, and T.D. Al bright, Afferent basis of visual response properties in area MT of the macaque: I. Effects of striate cortex removal, Journal of Neuroscience, 9, 2033 (1989). 7. A. Cowey, P. Stoerig, and V.H. Perry, Trans neuronal retrograde degeneration of retinal ganglion cells after damage to striate cortex in macaque mon keys: Selective loss of P-beta cells, Neuroscience, 29,65 (1989). 8. D.C Dennett, Consciousness Explained (Pen guin Press, London, 1991). 9. L. Weiskrantz, j.L. Barbur, and A. Sahraie, Parameters affecting conscious versus unconscious visual discrimination with damage to the visual corI tex (V1), Proceedings of the National Academy of Science, U.S.A., 92, 6122-6126 (1995).
TL;DR: In this article, the authors used measures of right amygdala neural activity acquired from volunteer subjects viewing masked fear-conditioned faces to determine whether a colliculo-pulvinar pathway was engaged during processing of these unseen target stimuli.
Abstract: Neuroimaging studies have shown differential amygdala responses to masked (“unseen”) emotional stimuli. How visual signals related to such unseen stimuli access the amygdala is unknown. A possible pathway, involving the superior colliculus and pulvinar, is suggested by observations of patients with striate cortex lesions who show preserved abilities to localize and discriminate visual stimuli that are not consciously perceived (“blindsight”). We used measures of right amygdala neural activity acquired from volunteer subjects viewing masked fear-conditioned faces to determine whether a colliculo-pulvinar pathway was engaged during processing of these unseen target stimuli. Increased connectivity between right amygdala, pulvinar, and superior colliculus was evident when fear-conditioned faces were unseen rather than seen. Right amygdala connectivity with fusiform and orbitofrontal cortices decreased in the same condition. By contrast, the left amygdala, whose activity did not discriminate seen and unseen fear-conditioned targets, showed no masking-dependent changes in connectivity with superior colliculus or pulvinar. These results suggest that a subcortical pathway to the right amygdala, via midbrain and thalamus, provides a route for processing behaviorally relevant unseen visual events in parallel to a cortical route necessary for conscious identification.