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  1. How and what does the cerebellum learn?Peter F. C. Gilbert - 1996 - Behavioral and Brain Sciences 19 (3):449-450.
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  • The cognitive map must be a separate module.Benjamin Kuipers - 1982 - Behavioral and Brain Sciences 5 (4):645-646.
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  • The special nature of spatial information.Michael Potegal - 1982 - Behavioral and Brain Sciences 5 (4):647-648.
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  • Functional architectures for cognition: are simple inferences possible?Steven W. Zucker - 1980 - Behavioral and Brain Sciences 3 (1):153-154.
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  • Plasticity: conceptual and neuronal.Paul M. Churchland - 1980 - Behavioral and Brain Sciences 3 (1):133-134.
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  • Psychology and computational architecture.John Haugeland - 1980 - Behavioral and Brain Sciences 3 (1):138-139.
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  • Symbolic invention: The missing (computational) link?Andy Clark - 1993 - Behavioral and Brain Sciences 16 (4):753-754.
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  • New wine in old glasses?Joseph M. Scandura - 1984 - Behavioral and Brain Sciences 7 (4):602-603.
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  • Is there such a thing as a problem situation?Kjell Raaheim - 1984 - Behavioral and Brain Sciences 7 (4):600-601.
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  • An operant analysis of problem solving.B. F. Skinner - 1984 - Behavioral and Brain Sciences 7 (4):583-591.
    Behavior that solves a problem is distinguished by the fact that it changes another part of the solver's behavior and is strengthened when it does so. Problem solving typically involves the construction of discriminative stimuli. Verbal responses produce especially useful stimuli, because they affect other people. As a culture formulates maxims, laws, grammar, and science, its members behave more effectively without direct or prolonged contact with the contingencies thus formulated. The culture solves problems for its members, and does so by (...)
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  • The centrality of instantiations.John A. Barnden - 1987 - Behavioral and Brain Sciences 10 (3):437-438.
    This paper is a commentary on the target article by Michael Arbib, “Levels of modeling of mechanisms of visually guided behavior”, in the same issue of the journal, pp. 407–465. -/- I focus on the importance of the inclusion of an ability of a system to entertain, at a given time, multiple instantiations of a given schema (situation template, frame, script, action plan, etc.), and complications introduced into neural/connectionist network systems by such inclusion.
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  • Levels of psychological reality, Arbib's “schemas,” and matters maybe metaphysical.Keith Gunderson - 1987 - Behavioral and Brain Sciences 10 (3):439-440.
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  • Connectionist Models and Their Properties.J. A. Feldman & D. H. Ballard - 1982 - Cognitive Science 6 (3):205-254.
    Much of the progress in the fields constituting cognitive science has been based upon the use of explicit information processing models, almost exclusively patterned after conventional serial computers. An extension of these ideas to massively parallel, connectionist models appears to offer a number of advantages. After a preliminary discussion, this paper introduces a general connectionist model and considers how it might be used in cognitive science. Among the issues addressed are: stability and noise‐sensitivity, distributed decision‐making, time and sequence problems, and (...)
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  • Computation and cognition: Issues in the foundation of cognitive science.Zenon W. Pylyshyn - 1980 - Behavioral and Brain Sciences 3 (1):111-32.
    The computational view of mind rests on certain intuitions regarding the fundamental similarity between computation and cognition. We examine some of these intuitions and suggest that they derive from the fact that computers and human organisms are both physical systems whose behavior is correctly described as being governed by rules acting on symbolic representations. Some of the implications of this view are discussed. It is suggested that a fundamental hypothesis of this approach is that there is a natural domain of (...)
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  • Language and psychological reality: A discussion of Rudolf Botha's study.Peter Slezak - 1981 - Synthese 49 (December):427-439.
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  • Voice, gesture and working memory in the emergence of speech.Francisco Aboitiz - 2018 - Interaction Studies. Social Behaviour and Communication in Biological and Artificial Systemsinteraction Studies / Social Behaviour and Communication in Biological and Artificial Systemsinteraction Studies 19 (1-2):70-85.
    Language and speech depend on a relatively well defined neural circuitry, located predominantly in the left hemisphere. In this article, I discuss the origin of the speech circuit in early humans, as an expansion of an auditory-vocal articulatory network that took place after the last common ancestor with the chimpanzee. I will attempt to converge this perspective with aspects of the Mirror System Hypothesis, particularly those related to the emergence of a meaningful grammar in human communication. Basically, the strengthening of (...)
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  • Further evidence for the involvement of nitric oxide in trans-ACPD-induced suppression of AMPA responses in cultured chick Purkinje neurons.Junko Mori-Okamoto & Koichi Okamoto - 1996 - Behavioral and Brain Sciences 19 (3):467-468.
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  • No more news from the cerebellum.Steven R. Vincent - 1996 - Behavioral and Brain Sciences 19 (3):490-492.
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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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  • Computation without representation.Stephen P. Stich - 1980 - Behavioral and Brain Sciences 3 (1):152-152.
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  • Reductionism and cognitive flexibility.Frank Keil - 1980 - Behavioral and Brain Sciences 3 (1):141-142.
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  • Archaeological evidence for mimetic mind and culture.Thomas Wynn - 1993 - Behavioral and Brain Sciences 16 (4):774-774.
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  • Learning from instruction.Jerome A. Feldman - 1984 - Behavioral and Brain Sciences 7 (4):593-593.
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  • Nitric oxide is involved in cerebellar long-term depression.Daisuke Okada - 1996 - Behavioral and Brain Sciences 19 (3):468-469.
    The involvement of nitric oxide in cerebellar long-term depression is supported by the observation that nitric oxide is released by climbing fiber stimulation and by pharmacological tool usage. Two forms of long-term depression should be distinguished by their physiological relevance. [CRÉPEL et al.; LINDEN; VINCENT].
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  • We know a lot about the cerebellum, but do we know what motor learning is?Stephan P. Swinnen, Charles B. Walter & Natalia Dounskaia - 1996 - Behavioral and Brain Sciences 19 (3):474-475.
    In the behavioral literature on human movement, a distinction is made between the learning of parameters and the learning of new movement forms or topologies. Whereas the target articles by Thach, Smith, and Houk et al. provide evidence for cerebellar involvement in parametrization learning and adaptation, the evidence in favor of its involvement in the generation of new movement patterns is less straightforward. A case is made for focusing more attention on the latter issue in the future. This would directly (...)
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  • Précis of Origins of the modern mind: Three stages in the evolution of culture and cognition.Merlin Donald - 1993 - Behavioral and Brain Sciences 16 (4):737-748.
    This bold and brilliant book asks the ultimate question of the life sciences: How did the human mind acquire its incomparable power? In seeking the answer, Merlin Donald traces the evolution of human culture and cognition from primitive apes to the era of artificial intelligence, and presents an original theory of how the human mind evolved from its presymbolic form. In the emergence of modern human culture, Donald proposes, there were three radical transitions. During the first, our bipedal but still (...)
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  • A bridge between cerebellar long-term depression and discrete motor learning: Studies on gene knockout mice.Masanobu Kano - 1996 - Behavioral and Brain Sciences 19 (3):488-490.
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  • On the evolution of representational capacities.Merlin Donald - 1993 - Behavioral and Brain Sciences 16 (4):775-791.
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  • “Pop science” versus understanding the emergence of the modern mind.C. Loring Brace - 1993 - Behavioral and Brain Sciences 16 (4):750-751.
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  • Schemas: Not yet an interlingua for the brain sciences.John K. Tsotsos - 1987 - Behavioral and Brain Sciences 10 (3):447-448.
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  • Human spatial learning.Kristina Hooper - 1982 - Behavioral and Brain Sciences 5 (4):642-643.
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  • Representations of the environment, multiple brain maps, and control systems.Charles M. Butter - 1982 - Behavioral and Brain Sciences 5 (4):640-641.
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  • Functional architecture and model validation.Martin Ringle - 1980 - Behavioral and Brain Sciences 3 (1):150-151.
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  • A remark on the completeness of the computational model of mind.William Demopoulos - 1980 - Behavioral and Brain Sciences 3 (1):135-135.
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  • External representation: An issue for cognition.Jiajie Zhang - 1993 - Behavioral and Brain Sciences 16 (4):774-775.
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  • Hunting memes.H. C. Plotkin - 1993 - Behavioral and Brain Sciences 16 (4):768-769.
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  • Memory, text and the Greek Revolution.Jocelyn Penny Small - 1993 - Behavioral and Brain Sciences 16 (4):769-770.
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  • The gradual evolution of enhanced control by plans: A view from below.Leonard D. Katz - 1993 - Behavioral and Brain Sciences 16 (4):764-765.
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  • The modern mind: Its missing parts?R. I. M. Dunbar - 1993 - Behavioral and Brain Sciences 16 (4):758-759.
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  • Rule-governed behavior in computational psychology.Edward P. Stabler - 1984 - Behavioral and Brain Sciences 7 (4):604-605.
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  • Schema theory: A broadening viewpoint.Tang Yi Qun - 1987 - Behavioral and Brain Sciences 10 (3):446-447.
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  • Sensory prediction as a role for the cerebellum.R. C. Miall, M. Malkmus & E. M. Robertson - 1996 - Behavioral and Brain Sciences 19 (3):466-467.
    We suggest that the cerebellum generates sensory or estimates based on outgoing motor commands and sensory feedback. Thus, it is not a motor pattern generator (HOUK et al.) but a predictive system which is intimately involved in motor behavior. This theory may explain the sensitivity of the climbing fibers to both unexpected external events and motor errors (SIMPSON et al.), and we speculate that unusual biophysical properties of the inferior olive might allow the cerebellum to develop multiple asynchronous sensory estimates, (...)
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  • More on climbing fiber signals and their consequence(s).J. I. Simpson, D. R. W. Wylie & C. I. De Zeeuw - 1996 - Behavioral and Brain Sciences 19 (3):496-498.
    Several themes can be identified in the commentaries. The first is that the climbing fibers may have more than one function; the second is that the climbing fibers provide sensory rather than motor signals. We accept the possibility that climbing fibers may have more than one function consequence(s)’ in the title. Until we know more about the function of the inhibitory input to the inferior olive from the cerebellar nuclei, which are motor structures, we have to keep open the possibility (...)
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  • Cellular mechanisms of long-term depression: From consensus to open questions.F. Crépel - 1996 - Behavioral and Brain Sciences 19 (3):488-488.
    The target article on cellular mechanisms of long-term depression appears to have been well received by most authors of the relevant commentaries. This may be due to the fact that this review aimed to give a general account of the topic, rather than just describe previous work of the present author. The present response accordingly only raises questions of major interest for future research.
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  • Stages versus continuity.Christopher Wills - 1993 - Behavioral and Brain Sciences 16 (4):773-773.
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  • Grasping schemas is (are) difficult.H. T. A. Whiting - 1987 - Behavioral and Brain Sciences 10 (3):450-451.
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  • Negation in Skinner's system.N. E. Wetherick - 1984 - Behavioral and Brain Sciences 7 (4):606-607.
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  • Plasticity of cerebro-cerebellar interactions in patients with cerebellar dysfunction.Karl Wessel - 1996 - Behavioral and Brain Sciences 19 (3):481-482.
    Studies comparing movement-related cortical potentials, post-excitatory inhibition after transcranial magnetic brain stimulation, and PET findings in normal controls and patients with cerebellar degeneration demonstrate plasticity of cerebro-cerebellar interactions and hereby support Thach's theory that the cerebellum has the ability to play a role in building behavioral context-response linkages and to build up appropriate responses from simpler constitutive elements, [THACH].
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  • Eyeblink conditioning, motor control, and the analysis of limbic-cerebellar interactions.Craig Weiss & John F. Disterhoft - 1996 - Behavioral and Brain Sciences 19 (3):479-481.
    Several target articles in this BBS special issue address the topic of cerebellar and olivary functions, especially as they pertain to motor earning. Another important topic is the neural interaction between the limbic system and the cerebellum during associative learning. In this commentary we present some of our data on olivo-cerebellar and limbic-cerebellar interactions during eyeblink conditioning. [HOUK et al.; SIMPSON et al.; THACH].
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  • Cognition is not computation, for the reasons that computers don't solve the mind-body problems.Walter B. Weimer - 1980 - Behavioral and Brain Sciences 3 (1):152-153.
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