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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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  • 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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  • 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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  • The time course of perceptual choice: The leaky, competing accumulator model.Marius Usher & James L. McClelland - 2001 - Psychological Review 108 (3):550-592.
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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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  • 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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  • 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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  • 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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  • 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 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • Hippocampus, space, and relations.Lynn Nadel - 1994 - Behavioral and Brain Sciences 17 (3):490-491.
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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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  • Neocortical memory traces.Earl K. Miller - 1994 - Behavioral and Brain Sciences 17 (3):488-489.
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  • Comparators, functions, and experiences.Harold Merskey - 1995 - Behavioral and Brain Sciences 18 (4):689-690.
    The comparator model is insufficient for three reasons. First, consciousness is involved in the process of comparison as well as in the output. Second, we still do not have enough neurophysiological information to match the events of consciousness, although such knowledge is growing. Third, the anatomical localisation proposed can be damaged bilaterally but consciousness will persist.
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  • The hippocampus: Relational processor or antiprocessor?Neil McNaughton - 1994 - Behavioral and Brain Sciences 17 (3):487-488.
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  • What exactly do amnesics fail to store normally?Andrew R. Mayes - 1994 - Behavioral and Brain Sciences 17 (3):486-487.
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  • Human consciousness: One of a kind.R. E. Lubow - 1995 - Behavioral and Brain Sciences 18 (4):689-689.
    To avoid teleological interpretations, it is important to make a distinction between functions and uses of consciousness, and to address questions concerning the consequences of consciousness. Assumptions about the phylogenetic distribution of consciousness are examined. It is concluded that there is some value in identifying consciousness an exclusively human attribute.
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  • Correlating mind and body.T. J. Lioyd-Jones, N. Donnelly & B. Weekes - 1995 - Behavioral and Brain Sciences 18 (4):688-688.
    Gray's integration of the different levels of description and explanation in his theory is problematic: The introduction of consciousness into his theorising consists of the mind-brain identity assumption, which tells us nothing new. There need not be correlations between levels of description. Gray's account does not extend beyond “brute” correlation. Integration must be achieved in a principled, mutually constraining way.
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  • Septohippocampal comparator: Consciousness generator or attention feedback loop?Marcel Kinsbourne - 1995 - Behavioral and Brain Sciences 18 (4):687-688.
    As Gray insists, his comparator model proposes a brute correlation only – of consciousness with septohippocampal output. I suggest that the comparator straddles a feedback loop that boosts the activation ofnovelrepresentations, thus helping them feature in present or recollected experience. Such a role in organizing conscious contents would transcend correlation and help explain how consciousness emerges from brain function.
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  • Hippocampus and memory for time.Raymond P. Kesner - 1994 - Behavioral and Brain Sciences 17 (3):485-486.
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  • How long do relational representations in the hippocampus last during classical eyelid conditioning?Donald B. Katz & Joseph E. Steinmetz - 1994 - Behavioral and Brain Sciences 17 (3):484-485.
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  • A call for greater concern regarding the underlying anatomy.Leonard E. Jarrard - 1994 - Behavioral and Brain Sciences 17 (3):483-484.
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  • Information synthesis in cortical areas as an important link in brain mechanisms of mind.Alexei M. Ivanitsky - 1995 - Behavioral and Brain Sciences 18 (4):686-687.
    To explore the mechanism of sensation correlations between EP component amplitude and signal detection indices were studied. The time of sensation coincided with the peak latency of those EP components that showed a correlation with both indices. The components presumably reflected information synthesis in projection cortical neurons. A mechanism providing the synthesis process is proposed.
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  • Mind – your head!R. P. Ingvaldsen & H. T. A. Whiting - 1995 - Behavioral and Brain Sciences 18 (4):685-686.
    Gray takes an information-processing paradigm as his departure point, invoking a comparator as part of the system. He concludes that consciousness is to be found “in” the comparator but is unable to point to how the comparison takes place. Thus, the comparator turns out not to be an entity arising out of brain research per se, but out of the logic of the paradigm. In this way, Gray both reinvents dualism and remains trapped in the language game of his own (...)
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  • Perspective, reflection, transparent explanation, and other minds.S. L. Hurley - 1995 - Behavioral and Brain Sciences 18 (4):684-685.
    Perspective and reflection have each been considered in some way basic to phenomenal consciousness. Each has possible evolutionary value, though neither seems sufficient for consciousness. Consider an account of consciousness in terms of the combination of perspective and reflection, its relationship to the problem of other minds, and its capacity to inherit evolutionary explanation from its components.
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  • Going from task descriptions to memory structures.Michael S. Humphreys & Simon Dennis - 1994 - Behavioral and Brain Sciences 17 (3):483-483.
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  • The localization of general memory functions.James A. Horel - 1994 - Behavioral and Brain Sciences 17 (3):482-482.
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  • Psychopathology and the discontinuity of conscious experience.David R. Hemsley - 1995 - Behavioral and Brain Sciences 18 (4):683-684.
    It is accepted that “primary awareness” may emerge from the integration of two classes of information. It is unclear, however, why this cannot take place within the comparator rather than in conjunction with feedback to the perceptual systems. The model has plausibility in relation to the continuity of conscious experience in the normal waking state and may be extended to encompass certain aspects of the “sense of self” which are frequently disrupted in psychotic patients.
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  • Hippocampal representations of DMS/DNMS in the rat.Robert E. Hampson & Sam A. Deadwyler - 1994 - Behavioral and Brain Sciences 17 (3):480-482.
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  • Hippocampal modulation of recognition, conditioning, timing, and space: Why so many functions?Stephen Grossberg - 1994 - Behavioral and Brain Sciences 17 (3):479-480.
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  • The contents of consciousness: A neuropsychological conjecture.Jeffrey A. Gray - 1995 - Behavioral and Brain Sciences 18 (4):659-76.
    Drawing on previous models of anxiety, intermediate memory, the positive symptoms of schizophrenia, and goal-directed behaviour, a neuropsychological hypothesis is proposed for the generation of the contents of consciousness. It is suggested that these correspond to the outputs of a comparator that, on a moment-by-moment basis, compares the current state of the organism's perceptual world with a predicted state. An outline is given of the information-processing functions of the comparator system and of the neural systems which mediate them. The hypothesis (...)
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  • Psychoarithmetic or pick your own?Jeffrey A. Gray, John Sinden & Helen Hodges - 1994 - Behavioral and Brain Sciences 17 (3):478-479.
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  • Consciousness and its (dis)contents.Jeffrey A. Gray - 1995 - Behavioral and Brain Sciences 18 (4):703-722.
    The first claim in the target article was that there is as yet no transparent, causal account of the relations between consciousness and brain-and-behaviour. That claim remains firm. The second claim was that the contents of consciousness consist, psychologically, of the outputs of a comparator system; the third consisted of a description of the brain mechanisms proposed to instantiate the comparator. In order to defend these claims against criticism, it has been necessary to clarify the distinction between consciousness-as-such and the (...)
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  • A step linking memory to understanding?Mark A. Good & Richard G. M. Morris - 1994 - Behavioral and Brain Sciences 17 (3):477-478.
  • A computational perspective on dissociating hippocampal and entorhinal function.Mark A. Gluck, Catherine E. Myers & James K. Goebel - 1994 - Behavioral and Brain Sciences 17 (3):476-477.
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  • In search of the engrammer.Joaquin M. Fuster - 1994 - Behavioral and Brain Sciences 17 (3):476-476.
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  • Consciousness is for other people.Chris Frith - 1995 - Behavioral and Brain Sciences 18 (4):682-683.
    Gray has expanded his account of schizophrenia to explain consciousness as well. His theory explains neither phenomenon adequately because he treats individual minds in isolation. The primary function of consciousness is to permit high level interactions with other conscious beings. The key symptoms of schizophrenia reflect a failure of this mechanism.
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  • On seeking the mythical fountain of consciousness.Jeffrey Foss - 1995 - Behavioral and Brain Sciences 18 (4):682-682.
    Because consciousness has an organizational, or functional, center, Gray supposes that there must be a corresponding physical center in the brain. He proposes further that since this center generates consciousness, ablating it would eliminate consciousness, while leaving behavior intact. But the center of consciousness is simply the product of the functional linkages among sensory input, memory, inner speech, and so on, and behavior.
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