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  1. Functional distinctions within the medical temporal lobe memory system: What is the evidence?Stuart Zola-Morgan & Pablo Alvarez - 1994 - Behavioral and Brain Sciences 17 (3):495-496.
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  • The return of the reinforcement theorists.C. D. L. Wynne - 1994 - Behavioral and Brain Sciences 17 (1):156-156.
  • The neuropsychology of schizophrenia: In step but not in time.Jonathan H. Williams - 1991 - Behavioral and Brain Sciences 14 (1):55-56.
  • 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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  • A mathematical theory of reinforcement: An unexpected place to find support for analogical memory coding.Donald M. Wilkie & Lisa M. Saksida - 1994 - Behavioral and Brain Sciences 17 (1):155-156.
  • The accumbens–substantia nigra pathway, mismatch and amphetamine.Ina Weiner - 1991 - Behavioral and Brain Sciences 14 (1):54-55.
  • Fifty years on: The new “principles of behavior”?J. H. Wearden - 1994 - Behavioral and Brain Sciences 17 (1):155-155.
  • How general is a general theory of reinforcement?Stephen F. Walker - 1994 - Behavioral and Brain Sciences 17 (1):154-155.
  • Positiwe and negatiwe symptoms, the hippocampus and P3.Peter H. Venables - 1991 - Behavioral and Brain Sciences 14 (1):53-54.
  • 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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  • 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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  • What do animal models of memory model?Endel Tulving & Hans J. Markowitsch - 1994 - Behavioral and Brain Sciences 17 (3):498-499.
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  • The hippocampus seen in the context of declarative and procedural control.Frederick Toates - 1996 - Behavioral and Brain Sciences 19 (4):771-772.
    Various apparently incompatible theories of hippocampal function have been proposed but integration is now needed. It is argued that the involvement of the hippocampus is most clearly seen when the animal needs to extrapolate beyond current sensory information. Such control can involve both the initiation of behaviour in the absence of appropriate sensory input and the inhibition of behaviour that might otherwise be triggered by current sensory input.
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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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  • A model of the hierarchy of behaviour, cognition, and consciousness.Frederick Toates - 2006 - Consciousness and Cognition 15 (1):75-118.
    Processes comparable in important respects to those underlying human conscious and non-conscious processing can be identified in a range of species and it is argued that these reflect evolutionary precursors of the human processes. A distinction is drawn between two types of processing: stimulus-based and higher-order. For ‘higher-order,’ in humans the operations of processing are themselves associated with conscious awareness. Conscious awareness sets the context for stimulus-based processing and its end-point is accessible to conscious awareness. However, the mechanics of the (...)
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  • Animal-centered models of reinforcement.William Timberlake - 1994 - Behavioral and Brain Sciences 17 (1):153-154.
  • Exploration and memory.Catherine Thinus-Blanc - 1988 - Behavioral and Brain Sciences 11 (3):552.
  • Neuropsychology of schizophrenia: The “hole” thing is wrong.Neal R. Swerdlow - 1991 - Behavioral and Brain Sciences 14 (1):51-53.
  • Don't leave the “un” off “consciousness”.Neal R. Swerdlow - 1995 - Behavioral and Brain Sciences 18 (4):699-700.
    Gray extrapolates from circuit models of psychopathology to propose neural substrates for the contents of consciousness. I raise three concerns: knowledge of synaptic arrangements may be inadequate to fully support his model; latent inhibition deficits in schizophrenia, a focus of this and related models, are complex and deserve replication; and this conjecture omits discussion of the neuropsychological basis for the contents of the unconscious.
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  • Short-term memory in human operant conditioning.Frode Svartdal - 1994 - Behavioral and Brain Sciences 17 (1):152-153.
  • 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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  • What is schizophrenia?Janice R. Stevens & James M. Gold - 1991 - Behavioral and Brain Sciences 14 (1):50-51.
  • 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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  • The scale of nature: Fitted parameters and dimensional correctness.D. W. Stephens - 1994 - Behavioral and Brain Sciences 17 (1):150-152.
  • A plausible theory marred by certain inconsistencies.Herbert E. Spohn - 1991 - Behavioral and Brain Sciences 14 (1):49-50.
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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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  • 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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  • Practical effects of response specification.Richard L. Shull - 1994 - Behavioral and Brain Sciences 17 (1):150-150.
  • Awareness and reinforcement.Charles P. Shimp - 1994 - Behavioral and Brain Sciences 17 (1):149-150.
  • 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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  • Consciousness beyond the comparator.Victor A. Shames & Timothy L. Hubbard - 1995 - Behavioral and Brain Sciences 18 (4):697-697.
    Gray's comparator model fails to provide an adequate explanation of consciousness for two reasons. First, it is based on a narrow definition of consciousness that excludes basic phenomenology and active functions of consciousness. Second, match/mismatch decisions can be made without producing an experience of consciousness. The model thus violates the sufficiency criterion.
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  • 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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  • A hippocampal theory of schizophrenia.Nestor A. Schmajuk & James J. DiCarlo - 1991 - Behavioral and Brain Sciences 14 (1):47-49.
  • Dopamine-GABA-cholinergic interactions and negative schizophrenic symptomatology.Martin Sarter - 1991 - Behavioral and Brain Sciences 14 (1):46-47.
  • The significance of the basal ganglia for schizophrenia.Reuven Sandyk & Stanley R. Kay - 1991 - Behavioral and Brain Sciences 14 (1):45-46.
  • What should a theory of schizophrenia be able to do?Kurt Salzinger - 1991 - Behavioral and Brain Sciences 14 (1):44-45.
  • Prospects for a cognitive neuroscience of consciousness.Antti Revonsuo - 1995 - Behavioral and Brain Sciences 18 (4):694-695.
    In this commentary, I point out some weaknesses in Gray's target article and, in the light of that discussion, I attempt to delineate the kinds of problem a cognitive neuroscience of consciousness faces on its way to a scientific understanding of subjective experience.
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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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  • Memory and the integration of response sequences.Phil Reed - 1994 - Behavioral and Brain Sciences 17 (1):148-149.
  • The cognitive unconscious: An evolutionary perspective.Arthur S. Reber - 1992 - Consciousness and Cognition 1 (2):93-133.
    In recent decades it has become increasingly clear that a substantial amount of cognitive work goes on independent of consciousness. The research has been carried out largely under two rubrics, implicit learning and implicit memory. The former has been concerned primarily with the acquisition of knowledge independent of awareness and the latter with the manner in which memories not readily available to conscious recall or recognition play a role in behavior; collectively these operations comprise the essential functions of the cognitive (...)
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  • Time to close the store?J. N. P. Rawlins - 1987 - Behavioral and Brain Sciences 10 (1):156-160.
  • Does it still make sense to develop a declarative memory theory of hippocampal function?J. N. P. Rawlins, R. M. J. Deacon, B. K. Yee & H. J. Cassaday - 1994 - Behavioral and Brain Sciences 17 (3):492-493.
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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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  • Neuro-developmental, brain imaging and psychophysiological perspectives on the neuropsychology of schizophrenia.Adrian Raine & Tyrone D. Cannon - 1991 - Behavioral and Brain Sciences 14 (1):43-44.
  • The elusive quale.Howard Rachlin - 1995 - Behavioral and Brain Sciences 18 (4):692-693.
    If sensations were behaviorally conceived, as they should be, as complex functional patterns of interaction between overt behavior and the environment, there would be no point in searching for them as instantaneous psychic elements within the brain or as internal products of the brain.
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  • From overt behavior to hypothetical behavior to memory: Inference in the wrong direction.Howard Rachlin - 1994 - Behavioral and Brain Sciences 17 (1):147-148.
  • A heuristically useful but empirically weak neuropsychological model of schizophrenia.M. Pisa & J. M. Cleghorn - 1991 - Behavioral and Brain Sciences 14 (1):42-43.
  • Why don't preschizophrenic children have delusions and hallucinations?Lyn Pilowsky & Robin M. Murray - 1991 - Behavioral and Brain Sciences 14 (1):41-42.
  • Problems and pitfalls for Killeen's mathematical principles of reinforcement.Joseph J. Pear - 1994 - Behavioral and Brain Sciences 17 (1):146-147.
  • A realistic model will be much more complex and will consider longitudinal neuropsychodevelopment.Terry Patterson - 1991 - Behavioral and Brain Sciences 14 (1):40-41.