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  1. Anxiety viewed from the upper brain stem: Though panic and fear yield trepidation, should both be called anxiety?Jaak Panksepp - 1982 - Behavioral and Brain Sciences 5 (3):495-496.
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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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  • 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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  • World graphs: A partial model of spatial behavior.Israel Lieblich & Michael A. Arbib - 1982 - Behavioral and Brain Sciences 5 (4):651-659.
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  • Ecologizing world graphs.Robert E. Shaw & Ennio Mingolla - 1982 - Behavioral and Brain Sciences 5 (4):648-650.
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  • Expectancy: The endogenous source of anticipatory activities, including “pseudoconditioned” responses.Patrick J. Sheafor - 1982 - Behavioral and Brain Sciences 5 (3):387-389.
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  • The heuristic value of representation.Thomas R. Zentall - 1982 - Behavioral and Brain Sciences 5 (3):393-394.
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  • Misrepresenting behaviorism.Marc N. Branch - 1982 - Behavioral and Brain Sciences 5 (3):372-373.
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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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  • Connectionism and implementation.Paul Smolensky - 1987 - Behavioral and Brain Sciences 10 (3):492-493.
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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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  • Rhythmic modulation of sensorimotor activity in phase with EEG waves.Barry R. Komisaruk & Kazue Semba - 1981 - Behavioral and Brain Sciences 4 (3):483-484.
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  • Neocortical activation and adaptive behavior: Cholinergic influences.P. Shiromani & William Fishbein - 1981 - Behavioral and Brain Sciences 4 (3):488-489.
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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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  • 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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  • Does hippocampal theta tell us anything about the neuropsychology of anxiety?Terry E. Robinson & Barbara A. Therrien - 1982 - Behavioral and Brain Sciences 5 (3):500-502.
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  • Maps, space, and places.Roger M. Downs - 1982 - Behavioral and Brain Sciences 5 (4):641-642.
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  • Multiple representations of space underlying behavior.Israel Lieblich & Michael A. Arbib - 1982 - Behavioral and Brain Sciences 5 (4):627-640.
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  • Representation: A concept that fills no gaps.Robert Epstein - 1982 - Behavioral and Brain Sciences 5 (3):377-378.
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  • The meaning of representation in animal memory.H. L. Roitblat - 1982 - Behavioral and Brain Sciences 5 (3):353-372.
    A representation is a remnant of previous experience that allows that experience to affect later behavior. This paper develops a metatheoretical view of representation and applies it to issues concerning representation in animals. To describe a representational system one must specify the following: thedomainor range of situations in the represented world to which the system applies; thecontentor set of features encoded and preserved by the system; thecodeor transformational rules relating features of the representation to the corresponding features of the represented (...)
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  • ‘Species-typicality’: Can individuals have typical parts?Timothy D. Johnston - 1981 - Behavioral and Brain Sciences 4 (2):291-292.
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  • Units “of” selection: The end of “of”?F. J. Odling-Smee & H. C. Plotkin - 1981 - Behavioral and Brain Sciences 4 (2):295-296.
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  • Underestimating the importance of the implementational level.Michael Van Kleeck - 1987 - Behavioral and Brain Sciences 10 (3):497-498.
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  • Weak versus strong claims about the algorithmic level.Paul S. Rosenbloom - 1987 - Behavioral and Brain Sciences 10 (3):490-490.
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  • Ambiguities in “the algorithmic level”.Alvin I. Goldman - 1987 - Behavioral and Brain Sciences 10 (3):484-485.
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  • A flawed analogy?James Hendler - 1987 - Behavioral and Brain Sciences 10 (3):485-486.
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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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  • 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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  • Memory processing by the brain: Subregionalization, species-dependency, and network character.Hans J. Markowitsch - 1985 - Behavioral and Brain Sciences 8 (3):506-507.
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  • Reticulo-cortical activity and behavior: A critique of the arousal theory and a new synthesis.C. H. Vanderwolf & T. E. Robinson - 1981 - Behavioral and Brain Sciences 4 (3):459-476.
    It is traditionally believed that cerebral activation (the presence of low voltage fast electrical activity in the neocortex and rhythmical slow activity in the hippocampus) is correlated with arousal, while deactivation (the presence of large amplitude irregular slow waves or spindles in both the neocortex and the hippocampus) is correlated with sleep or coma. However, since there are many exceptions, these generalizations have only limited validity. Activated patterns occur in normal sleep (active or paradoxical sleep) and during states of anesthesia (...)
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  • Can the decomposition of attention clarify some clinical issues?Enoch Callaway - 1981 - Behavioral and Brain Sciences 4 (3):477-479.
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  • Behavioral problems related to the interpretation of brain rhythms.György Buzsáki, Robert L. Isaacson & John H. Hannigan - 1981 - Behavioral and Brain Sciences 4 (3):477-477.
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  • Modelling Animal Creativity from Uexküllian Approach—Attention, Search Image and Search Tone.Siiri Tarrikas - 2022 - Biosemiotics 15 (3):531-553.
    In this article, creativity is defined as a semiotic phenomenon, as a process in which the boundaries of habits and norms of social communication are exceeded and by which the challenges offered by the environment are solved. Here it is indicated that there is a direct link between attention and animal creativity and shown that there are at least two possibilities for creativity to work – one that needs attention and one which doesn’t. Animal creativity can work through several different (...)
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  • Substrates of anxiety: But if the starting point is wrong?Holger Ursin - 1982 - Behavioral and Brain Sciences 5 (3):503-504.
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  • The logic of representation.William W. Rozeboom - 1982 - Behavioral and Brain Sciences 5 (3):385-386.
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  • The informational character of representations.Fred Dretske - 1982 - Behavioral and Brain Sciences 5 (3):376-377.
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  • Biopopulations, not biospecies, are individuals and evolve.Mario Bunge - 1981 - Behavioral and Brain Sciences 4 (2):284-285.
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  • Three-store theories of memory.William S. Maki - 1985 - Behavioral and Brain Sciences 8 (3):505-506.
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  • On computer science, visual science, and the physiological utility of models.Barry J. Richmond & Michael E. Goldberg - 1985 - Behavioral and Brain Sciences 8 (2):300-301.
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  • Is the hippocampus a store, intermediate or otherwise?Neil McNaughton - 1985 - Behavioral and Brain Sciences 8 (3):508-509.
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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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  • Behaviorism and voluntarism.O. S. Vinogradova - 1981 - Behavioral and Brain Sciences 4 (3):496-497.
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  • An atropine-sensitive and a less atropine-sensitive system.Robert P. Vertes - 1981 - Behavioral and Brain Sciences 4 (3):493-494.
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  • Putting anxiety in its place?Daniel P. Kimble - 1982 - Behavioral and Brain Sciences 5 (3):489-489.
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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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  • Metatheory of animal behavior.Erwin M. Segal - 1982 - Behavioral and Brain Sciences 5 (3):386-387.
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  • Some distinctions among representations.M. Gopnik - 1982 - Behavioral and Brain Sciences 5 (3):378-379.
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  • On the hippocampus, time, and interference.Leonard E. Jarrard - 1985 - Behavioral and Brain Sciences 8 (3):503-504.
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  • Universals, particulars, and paradigms.Helen Heise - 1981 - Behavioral and Brain Sciences 4 (2):289-290.
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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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