Switch to: References

Add citations

You must login to add citations.
  1. Two functional components of the hippocampal memory system.Howard Eichenbaum, Tim Otto & Neal J. Cohen - 1994 - Behavioral and Brain Sciences 17 (3):449-472.
    There is considerable evidence that the hippocampal system contributes both to (1) the temporary maintenance of memories and to (2) the processing of a particular type of memory representation. The findings on amnesia suggest that these two distinguishing features of hippocampal memory processing are orthogonal. Together with anatomical and physiological data, the neuropsychological findings support a model of cortico-hippocampal interactions in which the temporal and representational properties of hippocampal memory processing are mediated separately. We propose that neocortical association areas maintain (...)
    Download  
     
    Export citation  
     
    Bookmark   143 citations  
  • Possible roles for a predictor plus comparator mechanism in human episodic recognition memory and imitative learning.Simon Dennis & Michael Humphreys - 1995 - Behavioral and Brain Sciences 18 (4):678-679.
    This commentary is divided into two parts. The first considers a possible role for Gray's predictor plus comparator mechanism in human episodic recognition memory. It draws on the computational specifications of recognition outlined in Humphreys et al. to demonstrate how the logically necessary components of recognition tasks might be mapped onto the mechanism. The second part demonstrates how the mechanism outlined by Gray might be implicated in a form of imitative learning suitable for the acquisition of complex tasks.
    Download  
     
    Export citation  
     
    Bookmark  
  • Overworking the hippocampus.Daniel C. Dennett - 1995 - Behavioral and Brain Sciences 18 (4):677-678.
    Gray mistakenly thinks I have rejected the sort of theoretical enterprise he is undertaking, because, according to him, I think that "more data" is all that is needed to resolve all the issues. Not at all. My stalking horse was the bizarre (often pathetic) claim that no amount of empirical, "third-person point-of-view" science (data plus theory) could ever reduce the residue of mystery about consciousness to zero. This "New Mysterianism" (Flanagan, 1991) is one that he should want to combat as (...)
    Download  
     
    Export citation  
     
    Bookmark   1 citation  
  • Hunting for consciousness in the brain: What is (the name of) the game?José-Luis Díaz - 1995 - Behavioral and Brain Sciences 18 (4):679-680.
    Robust theories concerning the connection between consciousness and brain function should derive not only from empirical evidence but also from a well grounded inind-body ontology. In the case of the comparator hypothesis, Gray develops his ideas relying extensively on empirical evidence, but he bounces irresolutely among logically incompatible metaphysical theses which, in turn, leads him to excessively skeptical conclusions concerning the naturalization of consciousness.
    Download  
     
    Export citation  
     
    Bookmark   3 citations  
  • Heterogeneity, orienting and habituation in schizophrenia.Michael E. Dawson & Erin A. Hazlett - 1991 - Behavioral and Brain Sciences 14 (1):24-25.
    Download  
     
    Export citation  
     
    Bookmark   5 citations  
  • What defines a legitimate issue for Skinnerian psychology: Philosophy or technology?Hank Davis - 1994 - Behavioral and Brain Sciences 17 (1):137-138.
    Download  
     
    Export citation  
     
    Bookmark  
  • The neuropsychology of schizophrenia: A perspective from neurobehavioral genetics.Wim E. Crusio - 1991 - Behavioral and Brain Sciences 14 (1):23-24.
    Download  
     
    Export citation  
     
    Bookmark  
  • The hunting of the hippocampal function.Wim E. Crusio - 1996 - Behavioral and Brain Sciences 19 (4):767-768.
    Eichenbaum et al.'s (1994a) theory suffers from a lack of ecological validation. It is not at all clear why the hypothesized faculties would have evolved and what their adaptive value would be. I argue that hippocampal function can only be understood if the animal is seen in its natural context.
    Download  
     
    Export citation  
     
    Bookmark  
  • Segmentalized consciousness in schizophrenia.Andrew Crider - 1995 - Behavioral and Brain Sciences 18 (4):676-677.
    Segmentalized consciousness in schizophrenia reflects a loss of the normal Gestalt organization and contextualization of perception. Grays model explains such segmentalization in terms of septohippocampal dysfunction, which is consistent with known neuropsychological impairment in schizophrenia. However, other considerations suggest that everyday perception and its failure in schizophrenia also involve prefrontal executive mechanisms, which are only minimally elaborated by Gray.
    Download  
     
    Export citation  
     
    Bookmark  
  • Motor disturbances in schizophrenia.Andrew Crider - 1991 - Behavioral and Brain Sciences 14 (1):22-23.
    Download  
     
    Export citation  
     
    Bookmark  
  • The limbic-striatal interaction: A seesaw rather than a tandem.A. R. Cools & B. Ellenbroek - 1991 - Behavioral and Brain Sciences 14 (1):22-22.
    Download  
     
    Export citation  
     
    Bookmark  
  • Hippocampus, delay neurons, and sensory heterogeneity.Michael Colombo & Charles G. Gross - 1996 - Behavioral and Brain Sciences 19 (4):766-767.
    We raise three issues concerning the Eichenbaum, Otto & Cohen (1994) model. (1) We argue against the strict division of labor that Eichenbaum et al. attribute to neocortical and limbic regions. (2) We raise the possibility that the anterior and posterior portions of the hippocampus may be important for different types of information processing. (3) We argue that, rather than reflecting relational processing, different neural responses to “match” and “nonmatch” trials may relate to different required spatial responses.
    Download  
     
    Export citation  
     
    Bookmark   1 citation  
  • Don't leave the “psyche” out of neuropsychology.Gordon Claridge & Tony Beech - 1991 - Behavioral and Brain Sciences 14 (1):21-21.
    Download  
     
    Export citation  
     
    Bookmark  
  • A faulty negative feedback control underlies the schizophrenic syndrome?Arvid Carlsson & Maria Carlsson - 1991 - Behavioral and Brain Sciences 14 (1):20-21.
    Download  
     
    Export citation  
     
    Bookmark  
  • Processing temporally discontiguous information is neither an exclusive nor the only function of the hippocampus.J. Bureš, O. Burešová & J. J. Bolhuis - 1987 - Behavioral and Brain Sciences 10 (1):154-156.
    Download  
     
    Export citation  
     
    Bookmark  
  • Recording the recognition due to the parahippocampal region places hippocampal relational encoding in context.M. W. Brown - 1994 - Behavioral and Brain Sciences 17 (3):474-476.
    Download  
     
    Export citation  
     
    Bookmark  
  • Validation of behavioural equations: Can neurobiology help?C. M. Bradshaw - 1994 - Behavioral and Brain Sciences 17 (1):136-137.
    Download  
     
    Export citation  
     
    Bookmark  
  • The response problem.Robert C. Bolles - 1994 - Behavioral and Brain Sciences 17 (1):135-136.
    Download  
     
    Export citation  
     
    Bookmark   2 citations  
  • The hippocampal system, time, and memory representations.J. J. Bolhuis & I. C. Reid - 1994 - Behavioral and Brain Sciences 17 (3):474-474.
    Download  
     
    Export citation  
     
    Bookmark  
  • Remembering spatial cognition as a hippocampal functional component.Verner P. Bingman - 1994 - Behavioral and Brain Sciences 17 (3):473-474.
    Download  
     
    Export citation  
     
    Bookmark   6 citations  
  • Is Eichenbaum et al.'s proposal testable and how extensive is the hippocampal memory system?John P. Aggleton - 1994 - Behavioral and Brain Sciences 17 (3):472-473.
    Download  
     
    Export citation  
     
    Bookmark   6 citations  
  • Episodic memory, amnesia, and the hippocampal–anterior thalamic axis.John P. Aggleton & Malcolm W. Brown - 1999 - Behavioral and Brain Sciences 22 (3):425-444.
    By utilizing new information from both clinical and experimental (lesion, electrophysiological, and gene-activation) studies with animals, the anatomy underlying anterograde amnesia has been reformulated. The distinction between temporal lobe and diencephalic amnesia is of limited value in that a common feature of anterograde amnesia is damage to part of an comprising the hippocampus, the fornix, the mamillary bodies, and the anterior thalamic nuclei. This view, which can be traced back to Delay and Brion (1969), differs from other recent models in (...)
    Download  
     
    Export citation  
     
    Bookmark   44 citations  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark   6 citations  
  • The return of the reinforcement theorists.C. D. L. Wynne - 1994 - Behavioral and Brain Sciences 17 (1):156-156.
    Download  
     
    Export citation  
     
    Bookmark  
  • The neuropsychology of schizophrenia: In step but not in time.Jonathan H. Williams - 1991 - Behavioral and Brain Sciences 14 (1):55-56.
    Download  
     
    Export citation  
     
    Bookmark  
  • Hippocampal neuronal activity in rat and primate: Memory and movement.Frasar A. W. Wilson - 1994 - Behavioral and Brain Sciences 17 (3):499-500.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark  
  • The accumbens–substantia nigra pathway, mismatch and amphetamine.Ina Weiner - 1991 - Behavioral and Brain Sciences 14 (1):54-55.
    Download  
     
    Export citation  
     
    Bookmark   5 citations  
  • Fifty years on: The new “principles of behavior”?J. H. Wearden - 1994 - Behavioral and Brain Sciences 17 (1):155-155.
    Download  
     
    Export citation  
     
    Bookmark  
  • How general is a general theory of reinforcement?Stephen F. Walker - 1994 - Behavioral and Brain Sciences 17 (1):154-155.
    Download  
     
    Export citation  
     
    Bookmark  
  • Positiwe and negatiwe symptoms, the hippocampus and P3.Peter H. Venables - 1991 - Behavioral and Brain Sciences 14 (1):53-54.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark   3 citations  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark   3 citations  
  • What do animal models of memory model?Endel Tulving & Hans J. Markowitsch - 1994 - Behavioral and Brain Sciences 17 (3):498-499.
    Download  
     
    Export citation  
     
    Bookmark   7 citations  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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 (...)
    Download  
     
    Export citation  
     
    Bookmark   8 citations  
  • Animal-centered models of reinforcement.William Timberlake - 1994 - Behavioral and Brain Sciences 17 (1):153-154.
    Download  
     
    Export citation  
     
    Bookmark   2 citations  
  • Exploration and memory.Catherine Thinus-Blanc - 1988 - Behavioral and Brain Sciences 11 (3):552.
    Download  
     
    Export citation  
     
    Bookmark  
  • Neuropsychology of schizophrenia: The “hole” thing is wrong.Neal R. Swerdlow - 1991 - Behavioral and Brain Sciences 14 (1):51-53.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark   1 citation  
  • Short-term memory in human operant conditioning.Frode Svartdal - 1994 - Behavioral and Brain Sciences 17 (1):152-153.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark  
  • What is schizophrenia?Janice R. Stevens & James M. Gold - 1991 - Behavioral and Brain Sciences 14 (1):50-51.
    Download  
     
    Export citation  
     
    Bookmark   38 citations  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark  
  • The scale of nature: Fitted parameters and dimensional correctness.D. W. Stephens - 1994 - Behavioral and Brain Sciences 17 (1):150-152.
    Download  
     
    Export citation  
     
    Bookmark  
  • A plausible theory marred by certain inconsistencies.Herbert E. Spohn - 1991 - Behavioral and Brain Sciences 14 (1):49-50.
    Download  
     
    Export citation  
     
    Bookmark  
  • What are the best strategies for understanding hippocampal function?Paul R. Solomon & Bo-Yi Yang - 1994 - Behavioral and Brain Sciences 17 (3):494-495.
    Download  
     
    Export citation  
     
    Bookmark  
  • 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.
    Download  
     
    Export citation  
     
    Bookmark  
  • Practical effects of response specification.Richard L. Shull - 1994 - Behavioral and Brain Sciences 17 (1):150-150.
    Download  
     
    Export citation  
     
    Bookmark