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Multiple memory systems: What and why, an update

In D. Schacter & E. Tulving (eds.), Memory Systems. MIT Press. pp. 1994--39 (1994)

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  1. 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.
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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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  • 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 (...)
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  • The reinterpretation of dreams: An evolutionary hypothesis of the function of dreaming.Antti Revonsuo - 2000 - Behavioral and Brain Sciences 23 (6):877-901.
    Several theories claim that dreaming is a random by-product of REM sleep physiology and that it does not serve any natural function. Phenomenal dream content, however, is not as disorganized as such views imply. The form and content of dreams is not random but organized and selective: during dreaming, the brain constructs a complex model of the world in which certain types of elements, when compared to waking life, are underrepresented whereas others are over represented. Furthermore, dream content is consistently (...)
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  • (1 other version)A unified framework for addiction: Vulnerabilities in the decision process.A. David Redish, Steve Jensen & Adam Johnson - 2008 - Behavioral and Brain Sciences 31 (4):415-437.
    The understanding of decision-making systems has come together in recent years to form a unified theory of decision-making in the mammalian brain as arising from multiple, interacting systems (a planning system, a habit system, and a situation-recognition system). This unified decision-making system has multiple potential access points through which it can be driven to make maladaptive choices, particularly choices that entail seeking of certain drugs or behaviors. We identify 10 key vulnerabilities in the system: (1) moving away from homeostasis, (2) (...)
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  • Consciousness, art, and the brain: Lessons from Marcel Proust.Russell Epstein - 2004 - Consciousness and Cognition 13 (2):213-40.
    In his novel Remembrance of Things Past, Marcel Proust argues that conventional descriptions of the phenomenology of consciousness are incomplete because they focus too much on the highly-salient sensory information that dominates each moment of awareness and ignore the network of associations that lies in the background. In this paper, I explicate Proust’s theory of conscious experience and show how it leads him directly to a theory of aesthetic perception. Proust’s division of awareness into two components roughly corresponds to William (...)
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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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  • 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 do animal models of memory model?Endel Tulving & Hans J. Markowitsch - 1994 - Behavioral and Brain Sciences 17 (3):498-499.
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  • Neocortical memory traces.Earl K. Miller - 1994 - Behavioral and Brain Sciences 17 (3):488-489.
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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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  • 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 localization of general memory functions.James A. Horel - 1994 - Behavioral and Brain Sciences 17 (3):482-482.
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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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  • Role of affective associations in the planning and habit systems of decision-making related to addiction.Marc T. Kiviniemi & Rick A. Bevins - 2008 - Behavioral and Brain Sciences 31 (4):450-451.
    The model proposed by Redish et al. considers vulnerabilities within decision systems based on expectancy-value assumptions. Further understanding of processes leading to addiction can be gained by considering other inputs to decision-making, particularly affective associations with behaviors. This consideration suggests additional decision-making vulnerabilities that might explain addictive behaviors.
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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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  • Multiple memory systems : a neurophilosophical analysis.Elizabeth Leigh Ennen - unknown
    Neuroscientific data may be usefully invoked in the arbitration of debates concerning the scope of representational theories of the mind. Contemporary cognitivists tend toward theoretical imperialism in that they argue that all types of intelligent behaviour, including perceptual-motor skills, can be explained within the framework of representationalism. Phenomenologists argue that the scope of cognitivism is not as vast as its proponents suppose. They claim that perceptual-motor skills are non-representational and thus fall beyond the purview of cognitivism. I argue that this (...)
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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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  • Aligning Multiple Research Techniques in Cognitive Neuroscience: Why Is It Important?William Bechtel - 2002 - Philosophy of Science 69 (S3):S48-S58.
    The need to align multiple experimental procedures and produce converging results so as to demonstrate that the phenomenon under investigation is real and not an artifact is a commonplace both in scientific practice and discussions of scientific methodology (Campbell and Stanley 1963; Wimsatt 1981). Although sometimes this is the purpose of aligning techniques, often there is a different purpose—multiple techniques are sought to supply different perspectives on the phenomena under investigation that need to be integrated to answer the questions scientists (...)
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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 hippocampal system, time, and memory representations.J. J. Bolhuis & I. C. Reid - 1994 - Behavioral and Brain Sciences 17 (3):474-474.
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  • 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.
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  • Reconciling reinforcement learning models with behavioral extinction and renewal: Implications for addiction, relapse, and problem gambling.A. David Redish, Steve Jensen, Adam Johnson & Zeb Kurth-Nelson - 2007 - Psychological Review 114 (3):784-805.
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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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  • Hippocampus, space, and relations.Lynn Nadel - 1994 - Behavioral and Brain Sciences 17 (3):490-491.
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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.
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  • The hippocampal memory system and its functional comments: Further explication and clarification.Howard Eichenbaum, Tim Otto & Neal J. Cohen - 1994 - Behavioral and Brain Sciences 17 (3):500-517.
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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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  • 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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  • 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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  • Remembering spatial cognition as a hippocampal functional component.Verner P. Bingman - 1994 - Behavioral and Brain Sciences 17 (3):473-474.
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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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  • 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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  • 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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  • 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 hippocampus: Relational processor or antiprocessor?Neil McNaughton - 1994 - Behavioral and Brain Sciences 17 (3):487-488.
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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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