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  1. Communication and consciousness: A neural network conjecture.N. A. Schmajuk & E. Axelrad - 1995 - Behavioral and Brain Sciences 18 (4):695-696.
    The communicative aspects of the contents of consciousness are analyzed in the framework of a neural network model of animal communication. We discuss some issues raised by Gray, such as the control of the contents of consciousness, the adaptive value of consciousness, conscious and unconscious behaviors, and the nature of a model's consciousness.
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  • On giving a more active and selective role to consciousness.Frederick Toates - 1995 - Behavioral and Brain Sciences 18 (4):700-701.
    An active role for conscious processes in the production of behaviour is proposed, involving top level controls in a hierarchy of behavioural control. It is suggested that by inhibiting or sensitizing lower levels in the hierarchy conscious processes can play a role in the organization of ongoing behaviour. Conscious control can be more or less evident, according to prevailing circumstances.
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  • Hippocampus, space, and relations.Lynn Nadel - 1994 - Behavioral and Brain Sciences 17 (3):490-491.
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  • The homunculus at home.J. David Smith - 1995 - Behavioral and Brain Sciences 18 (4):697-698.
    In Gray's conjecture, mismatches in the subicular comparator and matches have equal prominence in consciousness. In rival cognitive views novelty and difficulty especially elicit more conscious modes of cognition and higher levels of self-regulation. The mismatch between Gray's conjecture and these views is discussed.
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  • The control of consciousness via a neuropsychological feedback loop.Todd D. Nelson - 1995 - Behavioral and Brain Sciences 18 (4):690-691.
    Gray's neuropsychological model of consciousness uses a hierarchical feedback loop framework that has been extensively discussed by many others in psychology. This commentary therefore urges Gray to integrate with, or at least acknowledge previous models. It also points out flaws in his feedback model and suggests directions for further theoretical work.
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  • Reticular-thalamic activation of the cortex generates conscious contents.James Newman - 1995 - Behavioral and Brain Sciences 18 (4):691-692.
    Gray hypothesizes that the contents of consciousness correspond to the outputs of a subicular (hippocampal/temporal lobe) comparator that compares the current state of the organism's perceptual world with a predicted state. I argue that Gray has identified a key contributing system to conscious awareness, but that his model is inadequate for explaining how conscious contents are generated in the brain. An alternative model is offered.
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  • Relational but not spatial memory: The task at hand.Elisabeth A. Murray - 1994 - Behavioral and Brain Sciences 17 (3):489-490.
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  • Ultimate differences.G. Lynn Stephens & George Graham - 1995 - Behavioral and Brain Sciences 18 (4):698-699.
    Gray unwisely melds together two distinguishable contributions of consciousness: one to epistemology, the other to evolution. He also renders consciousness needlessly invisible behaviorally.
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  • What can neuroanatomy tell us about the functional components of the hippocampal memory system?Wendy A. Suzuki - 1994 - Behavioral and Brain Sciences 17 (3):496-498.
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  • Unitary consciousness requires distributed comparators and global mappings.George N. Reeke - 1995 - Behavioral and Brain Sciences 18 (4):693-694.
    Gray, like other recent authors, seeks a scientific approach to consciousness, but fails to provide a biologically convincing description, partly because he implicitly bases his model on a computationalist foundation that embeds the contents of thought in irreducible symbolic representations. When patterns of neural activity instantiating conscious thought are shorn of homuncular observers, it appears most likely that these patterns and the circuitry that compares them with memories and plans should be found distributed over large regions of neocortex.
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  • Consciousness does not seem to be linked to a single neural mechanism.Carlo Umiltà & Marco Zorzi - 1995 - Behavioral and Brain Sciences 18 (4):701-702.
    On the basis of neuropsychological evidence, it is clear that attention should be given a role in any model of consciousness. What is known about the many instances of dissociation between explicit and implicit knowledge after brain damage suggests that conscious experience might not be linked to a restricted area of the brain. Even if it were true that there is a single brain area devoted to consciousness, the subicular area would seem to be an unlikely possibility.
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  • Functional components of the hippocampal memory system: Implications for future learning and memory research in nonhuman primates.Peter R. Rapp - 1994 - Behavioral and Brain Sciences 17 (3):491-492.
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  • From Heisenberg's cat to Eichenbaum's rat: Uncertainty in predicting the neural requirements for animal behavior.Matthew L. Shapiro - 1994 - Behavioral and Brain Sciences 17 (3):493-494.
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  • The limits of neuropsychological models of consciousness.Max Velmans - 1995 - Behavioral and Brain Sciences 18 (4):702-703.
    This commentary elaborates on Gray's conclusion that his neurophysiological model of consciousness might explain how consciousness arises from the brain, but does not address how consciousness evolved, affects behaviour or confers survival value. The commentary argues that such limitations apply to all neurophysiological or other third-person perspective models. To approach such questions the first-person nature of consciousness needs to be taken seriously in combination with third-person models of the brain.
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  • What are the best strategies for understanding hippocampal function?Paul R. Solomon & Bo-Yi Yang - 1994 - Behavioral and Brain Sciences 17 (3):494-495.
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  • Hippocampal neuronal activity in rat and primate: Memory and movement.Frasar A. W. Wilson - 1994 - Behavioral and Brain Sciences 17 (3):499-500.
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