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  1. Reticular formation, brain waves, and coma.George G. Somjen - 1981 - Behavioral and Brain Sciences 4 (3):489-489.
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  • Independent forebrain and brainstem controls for arousal and sleep.Jaime R. Villablanca - 1981 - Behavioral and Brain Sciences 4 (3):494-496.
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  • Integrating the literature on anxiety, memory, and the hippocampus.Susan D. Iversen - 1982 - Behavioral and Brain Sciences 5 (3):487-488.
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  • The relationship between memory and anxiety.J. N. P. Rawlins - 1982 - Behavioral and Brain Sciences 5 (3):498-499.
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  • Antianxiety and opiates.Mark S. Gold & Corinne Frantz Fox - 1982 - Behavioral and Brain Sciences 5 (3):486-487.
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  • Looking for nodes and edges.Arnold Trehub - 1982 - Behavioral and Brain Sciences 5 (4):650-651.
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  • Memory representations in animals: Some metatheoretical issues.Roy Lachman & Janet L. Lachman - 1982 - Behavioral and Brain Sciences 5 (3):380-381.
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  • Historicism, behaviorism, and the conceptual status of memory representations in animals.Charles P. Shimp - 1982 - Behavioral and Brain Sciences 5 (3):389-390.
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  • In the beginning was the word.J. E. R. Staddon - 1982 - Behavioral and Brain Sciences 5 (3):390-391.
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  • The informational character of representations.Fred Dretske - 1982 - Behavioral and Brain Sciences 5 (3):376-377.
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  • Metaphysics and common usage.David L. Hull - 1981 - Behavioral and Brain Sciences 4 (2):290-291.
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  • Natural categories and natural concepts.Frank C. Keil - 1981 - Behavioral and Brain Sciences 4 (2):293-294.
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  • What does Ghiselin mean by “individual”?Joseph B. Kruskal - 1981 - Behavioral and Brain Sciences 4 (2):294-295.
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  • The demise of mental representations.Edward S. Reed - 1981 - Behavioral and Brain Sciences 4 (2):297-298.
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  • The metaphysics of individuality and its consequences for systematic biology.E. O. Wiley - 1981 - Behavioral and Brain Sciences 4 (2):302-303.
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  • Pick your poison: Historicism, essentialism, and emergentism in the definition of species.Arthur L. Caplan - 1981 - Behavioral and Brain Sciences 4 (2):285-286.
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  • Categories, life, and thinking.Michael T. Ghiselin - 1981 - Behavioral and Brain Sciences 4 (2):269-283.
    Classifying is a fundamental operation in the acquisition of knowledge. Taxonomic theory can help students of cognition, evolutionary psychology, ethology, anatomy, and sociobiology to avoid serious mistakes, both practical and theoretical. More positively, it helps in generating hypotheses useful to a wide range of disciplines. Composite wholes, such as species and societies, are “individuals” in the logical sense, and should not be treated as if they were classes. A group of analogous features is a natural kind, but a group of (...)
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  • The hippocampal system: Dissociating its functional components and recombining them in the service of declarative memory.Howard Eichenbaum, Tim Otto & Neal J. Cohen - 1996 - Behavioral and Brain Sciences 19 (4):772-776.
    Continuing commentary raised several issues concerning our proposal that the hippocampus, parahippocampal region, and cortical association areas mediate different aspects of memory function. Recent relevant findings strengthen our argument that neocortical areas and the parahippocampal region maintain persistent encodings of specific single items and that the hippocampus mediates representations of the relations among these items. The reciprocally and closely interconnected structures that compose the hippocampal memory system work interactively to support flexible memory expression that is relevant to the natural behavior (...)
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  • Sequential processing of “items” and “relations”.Dave G. Mumby - 1996 - Behavioral and Brain Sciences 19 (4):770-771.
    Eichenbaum et al. (1994a) hypothesized that perceptually distinct items and the relations among them are processed sequentially by the parahippocampal region and the hippocampal formation, respectively. Predictions based solely on their model's sequential-processing feature might prove easier to disconfirm than those based on its representational features. Two such predictions are discussed: (1) double dissociations should be impossible following hippocampal vs. parahippocampal lesions, and (2) hippocampal lesions should not exacerbate impairments that follow complete parahippocampal lesions.
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  • Three frames suffice.Geoffrey E. Hinton - 1985 - Behavioral and Brain Sciences 8 (2):296-297.
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  • Does our behavioral methodology conceal the deficit caused by hippocampal damage?David T. D. James - 1985 - Behavioral and Brain Sciences 8 (3):502-503.
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  • The hippocampus as episodic encoder: Does it play tag?Robert H. I. Dale - 1985 - Behavioral and Brain Sciences 8 (3):499-500.
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  • Three frames suffice: Drop the retinotopic frame.Ralph Norman Haber - 1985 - Behavioral and Brain Sciences 8 (2):295-296.
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  • Cellular mechanisms of cholinergic arousal.K. Krnjević - 1981 - Behavioral and Brain Sciences 4 (3):484-485.
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  • Brain-behavioral studies: The importance of staying close to the data.C. H. Vanderwolf & T. E. Robinson - 1981 - Behavioral and Brain Sciences 4 (3):497-514.
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  • Four frames suffice: A provisional model of vision and space.Jerome A. Feldman - 1985 - Behavioral and Brain Sciences 8 (2):265-289.
    This paper presents a general computational treatment of how mammals are able to deal with visual objects and environments. The model tries to cover the entire range from behavior and phenomenological experience to detailed neural encodings in crude but computationally plausible reductive steps. The problems addressed include perceptual constancies, eye movements and the stable visual world, object descriptions, perceptual generalizations, and the representation of extrapersonal space.The entire development is based on an action-oriented notion of perception. The observer is assumed to (...)
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  • A ghost in a different guise.R. J. Sutherland, I. Q. Whishaw & B. Kolb - 1981 - Behavioral and Brain Sciences 4 (3):492-492.
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  • On mapping anxiety.Jeffrey A. Gray - 1982 - Behavioral and Brain Sciences 5 (3):506-534.
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  • Inhibition, attention, and the hippocampus.Andrew Crider & Paul R. Solomon - 1982 - Behavioral and Brain Sciences 5 (3):484-485.
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  • Human spatial learning.Kristina Hooper - 1982 - Behavioral and Brain Sciences 5 (4):642-643.
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  • Some thoughts on the proper foundations for the study of cognition in animals.Lynn Nadel - 1982 - Behavioral and Brain Sciences 5 (3):383-384.
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  • Misrepresenting behaviorism.Marc N. Branch - 1982 - Behavioral and Brain Sciences 5 (3):372-373.
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  • Species as individuals: Logical, biological, and philosophical problems.Michael Ruse - 1981 - Behavioral and Brain Sciences 4 (2):299-300.
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  • The world represented as a hierarchy of nature may not require “species”.Stanley N. Salthe - 1981 - Behavioral and Brain Sciences 4 (2):300-301.
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  • Associations across time: The hippocampus as a temporary memory store.J. N. P. Rawlins - 1985 - Behavioral and Brain Sciences 8 (3):479-497.
    All recent memory theories of hippocampal function have incorporated the idea that the hippocampus is required to process items only of some qualitatively specifiahle kind, and is not required to process items of some complementary set. In contrast, it is now proposed that the hippocampus is needed to process stimuli of all kinds, but only when there is a need to associate those stimuli with other events that are temporally discontiguous. In order to form or use temporally discontiguous associations, it (...)
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  • A physiological basis for hippocampal involvement in coding temporally discontiguous events.Sam A. Deadwyler - 1985 - Behavioral and Brain Sciences 8 (3):500-501.
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  • Is a behaviorist's approach sufficient for understanding the brain?Thomas L. Bennett - 1981 - Behavioral and Brain Sciences 4 (3):476-477.
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  • On novelty, places, and the septo-hippocampal system.Lynn Nadel & Richard Morris - 1982 - Behavioral and Brain Sciences 5 (3):493-494.
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  • Functions of the septo-hippocampal system.David S. Olton - 1982 - Behavioral and Brain Sciences 5 (3):494-495.
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  • The dynamics of action and the neuropsychology of anxiety.William Revelle - 1982 - Behavioral and Brain Sciences 5 (3):499-499.
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  • Précis of The neuropsychology of anxiety: An enquiry into the functions of the septo-hippocampal system.Jeffrey A. Gray - 1982 - Behavioral and Brain Sciences 5 (3):469-484.
    A model of the neuropsychology of anxiety is proposed. The model is based in the first instance upon an analysis of the behavioural effects of the antianxiety drugs in animals. From such psychopharmacologi-cal experiments the concept of a “behavioural inhibition system” has been developed. This system responds to novel stimuli or to those associated with punishment or nonreward by inhibiting ongoing behaviour and increasing arousal and attention to the environment. It is activity in the BIS that constitutes anxiety and that (...)
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  • Lost in Chelm: Maladaptive behavior in an adaptive model.Stephen Kaplan - 1982 - Behavioral and Brain Sciences 5 (4):643-644.
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  • Metatheory of animal behavior.Erwin M. Segal - 1982 - Behavioral and Brain Sciences 5 (3):386-387.
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  • Animal versus human minds.H. S. Terrace - 1982 - Behavioral and Brain Sciences 5 (3):391-392.
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  • Memory and rules in animal serial learning.E. J. Capaldi - 1982 - Behavioral and Brain Sciences 5 (3):373-373.
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  • The scientific induction problem: A case for case studies.K. Anders Ericsson - 1987 - Behavioral and Brain Sciences 10 (3):480-481.
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  • Methodologies for studying human knowledge.John R. Anderson - 1987 - Behavioral and Brain Sciences 10 (3):467-477.
    The appropriate methodology for psychological research depends on whether one is studying mental algorithms or their implementation. Mental algorithms are abstract specifications of the steps taken by procedures that run in the mind. Implementational issues concern the speed and reliability of these procedures. The algorithmic level can be explored only by studying across-task variation. This contrasts with psychology's dominant methodology of looking for within-task generalities, which is appropriate only for studying implementational issues.The implementation-algorithm distinction is related to a number of (...)
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  • 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.
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  • Does connectionism suffice?Steven W. Zucker - 1985 - Behavioral and Brain Sciences 8 (2):301-302.
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  • Effects of hippocampal lesions on some operant visual discrimination tasks.Michael L. Woodruff & Dennis L. Whittington - 1985 - Behavioral and Brain Sciences 8 (3):513-514.
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