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  1. How does the nervous system control the equilibrium trajectory?S. V. Adamovich - 1992 - Behavioral and Brain Sciences 15 (4):704-705.
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  • Implications of neural networks for how we think about brain function.David A. Robinson - 1992 - Behavioral and Brain Sciences 15 (4):644-655.
    Engineers use neural networks to control systems too complex for conventional engineering solutions. To examine the behavior of individual hidden units would defeat the purpose of this approach because it would be largely uninterpretable. Yet neurophysiologists spend their careers doing just that! Hidden units contain bits and scraps of signals that yield only arcane hints about network function and no information about how its individual units process signals. Most literature on single-unit recordings attests to this grim fact. On the other (...)
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  • Not all reflexive reasoning is deductive.Graeme Hirst & Dekai Wu - 1993 - Behavioral and Brain Sciences 16 (3):462-463.
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  • Synchronization and cognitive carpentry: From systematic structuring to simple reasoning. E. Koerner - 1993 - Behavioral and Brain Sciences 16 (3):465-466.
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  • Time phases, pointers, rules and embedding.John A. Barnden - 1993 - Behavioral and Brain Sciences 16 (3):451-452.
    This paper is a commentary on the target article by Lokendra Shastri & Venkat Ajjanagadde [S&A]: “From simple associations to systematic reasoning: A connectionist representation of rules, variables and dynamic bindings using temporal synchrony” in same issue of the journal, pp.417–451. -/- It puts S&A's temporal-synchrony binding method in a broader context, comments on notions of pointing and other ways of associating information - in both computers and connectionist systems - and mentions types of reasoning that are a challenge to (...)
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  • Does the nervous system depend on kinesthetic information to control natural limb movements?S. C. Gandevia & David Burke - 1992 - Behavioral and Brain Sciences 15 (4):614-632.
    This target article draws together two groups of experimental studies on the control of human movement through peripheral feedback and centrally generated signals of motor commands. First, during natural movement, feedback from muscle, joint, and cutaneous afferents changes; in human subjects these changes have reflex and kinesthetic consequences. Recent psychophysical and microneurographic evidence suggests that joint and even cutaneous afferents may have a proprioceptive role. Second, the role of centrally generated motor commands in the control of normal movements and movements (...)
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  • Do simple associations lead to systematic reasoning?Steven Sloman - 1993 - Behavioral and Brain Sciences 16 (3):471-472.
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  • The representation of egocentric space in the posterior parietal cortex.J. F. Stein - 1992 - Behavioral and Brain Sciences 15 (4):691-700.
    The posterior parietal cortex (PPC) is the most likely site where egocentric spatial relationships are represented in the brain. PPC cells receive visual, auditory, somaesthetic, and vestibular sensory inputs; oculomotor, head, limb, and body motor signals; and strong motivational projections from the limbic system. Their discharge increases not only when an animal moves towards a sensory target, but also when it directs its attention to it. PPC lesions have the opposite effect: sensory inattention and neglect. The PPC does not seem (...)
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  • Phase logic is biologically relevant logic.Gary W. Strong - 1993 - Behavioral and Brain Sciences 16 (3):472-473.
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  • Should first-order logic be neurally plausible?David S. Touretzky & Scott E. Fahlman - 1993 - Behavioral and Brain Sciences 16 (3):474-475.
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  • Plausible inference and implicit representation.Malcolm I. Bauer - 1993 - Behavioral and Brain Sciences 16 (3):452-453.
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  • From simple associations to systematic reasoning: A connectionist representation of rules, variables, and dynamic binding using temporal synchrony.Lokendra Shastri & Venkat Ajjanagadde - 1993 - Behavioral and Brain Sciences 16 (3):417-51.
    Human agents draw a variety of inferences effortlessly, spontaneously, and with remarkable efficiency – as though these inferences were a reflexive response of their cognitive apparatus. Furthermore, these inferences are drawn with reference to a large body of background knowledge. This remarkable human ability seems paradoxical given the complexity of reasoning reported by researchers in artificial intelligence. It also poses a challenge for cognitive science and computational neuroscience: How can a system of simple and slow neuronlike elements represent a large (...)
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  • Equilibrium-point hypothesis, minimum effort control strategy and the triphasic muscle activation pattern.Ning Lan & Patrick E. Crago - 1992 - Behavioral and Brain Sciences 15 (4):769-771.
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  • Does the nervous system use equilibrium-point control to guide single and multiple joint movements?E. Bizzi, N. Hogan, F. A. Mussa-Ivaldi & S. Giszter - 1992 - Behavioral and Brain Sciences 15 (4):603-613.
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  • Making reasoning more reasonable: Event-coherence and assemblies.Günther Palm - 1993 - Behavioral and Brain Sciences 16 (3):470-470.
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  • Temporal synchrony and the speed of visual processing.Simon J. Thorpe - 1993 - Behavioral and Brain Sciences 16 (3):473-474.
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  • Computational and biological constraints in the psychology of reasoning.Mike Oaksford & Mike Malloch - 1993 - Behavioral and Brain Sciences 16 (3):468-469.
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  • Making a middling mousetrap.Michael R. W. Dawson & Istvan Berkeley - 1993 - Behavioral and Brain Sciences 16 (3):454-455.
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  • Dynamical Emergence Theory (DET): A Computational Account of Phenomenal Consciousness.Roy Moyal, Tomer Fekete & Shimon Edelman - 2020 - Minds and Machines 30 (1):1-21.
    Scientific theories of consciousness identify its contents with the spatiotemporal structure of neural population activity. We follow up on this approach by stating and motivating Dynamical Emergence Theory, which defines the amount and structure of experience in terms of the intrinsic topology and geometry of a physical system’s collective dynamics. Specifically, we posit that distinct perceptual states correspond to coarse-grained macrostates reflecting an optimal partitioning of the system’s state space—a notion that aligns with several ideas and results from computational neuroscience (...)
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  • Useful ideas for exploiting time to engineer representations.Richard Rohwer - 1993 - Behavioral and Brain Sciences 16 (3):471-471.
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  • Deconstruction of neural data yields biologically implausible periodic oscillations.Walter J. Freeman - 1993 - Behavioral and Brain Sciences 16 (3):458-459.
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  • Reasoning, learning and neuropsychological plausibility.Joachim Diederich - 1993 - Behavioral and Brain Sciences 16 (3):455-456.
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  • Dynamic bindings by real neurons: Arguments from physiology, neural network models and information theory.Reinhard Eckhorn - 1993 - Behavioral and Brain Sciences 16 (3):457-458.
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  • Chaotic itinerancy is a key to mental diversity.Ichiro Tsuda - 2004 - Behavioral and Brain Sciences 27 (4):586-587.
    Kampis proposes the study of chaotic itinerancy, pointing out its significance in domains of cognitive science and philosophy. He has discovered in the concept of chaotic itinerancy the possibility for a new dynamical approach that elucidates mental states with a physical basis. This approach may therefore provide the means to go beyond the connectionist approach. In accordance with his theory, I here highlight three issues regarding chaotic itinerancy: transitory dynamics, diversity, and self-modifying system.
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  • Connectionism and syntactic binding of concepts.Georg Dorffner - 1993 - Behavioral and Brain Sciences 16 (3):456-457.
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  • Self-organizing neural models of categorization, inference and synchrony.Stephen Grossberg - 1993 - Behavioral and Brain Sciences 16 (3):460-461.
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  • Could static binding suffice?Paul R. Cooper - 1993 - Behavioral and Brain Sciences 16 (3):453-454.
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  • The cerebellum and memory.Richard F. Thompson - 1992 - Behavioral and Brain Sciences 15 (4):801-802.
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  • Psychological implications of the synchronicity hypothesis.Stellan Ohlsson - 1993 - Behavioral and Brain Sciences 16 (3):469-469.
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  • Distributing structure over time.John E. Hummel & Keith J. Holyoak - 1993 - Behavioral and Brain Sciences 16 (3):464-464.
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  • Is stiffness the mainspring of posture and movement?Z. Hasan - 1992 - Behavioral and Brain Sciences 15 (4):756-758.
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  • Reflections on reflexive reasoning.David L. Martin - 1993 - Behavioral and Brain Sciences 16 (3):466-466.
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  • Rule acquisition and variable binding: Two sides of the same coin.P. J. Hampson - 1993 - Behavioral and Brain Sciences 16 (3):462-462.
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  • A step toward modeling reflexive reasoning.Lokendra Shastri & Venkat Ajjanagadde - 1993 - Behavioral and Brain Sciences 16 (3):477-494.
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  • Toward a unified behavioral and brain science.Jerome A. Feldman - 1993 - Behavioral and Brain Sciences 16 (3):458-458.
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  • What we know and the LTKB.Stanley Munsat - 1993 - Behavioral and Brain Sciences 16 (3):466-467.
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  • Ethereal oscillations.Malcolm P. Young - 1993 - Behavioral and Brain Sciences 16 (3):476-477.
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  • Dynamic-binding theory is not plausible without chaotic oscillation.Ichiro Tsuda - 1993 - Behavioral and Brain Sciences 16 (3):475-476.
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  • On the artificial intelligence paradox.Steffen Hölldobler - 1993 - Behavioral and Brain Sciences 16 (3):463-464.
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  • Competing, or perhaps complementary, approaches to the dynamic-binding problem, with similar capacity limitations.Graeme S. Halford - 1993 - Behavioral and Brain Sciences 16 (3):461-462.
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  • Must we solve the binding problem in neural hardware?James W. Garson - 1993 - Behavioral and Brain Sciences 16 (3):459-460.
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  • From symbols to neurons: Are we there yet?Garrison W. Cottrell - 1993 - Behavioral and Brain Sciences 16 (3):454-454.
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  • Successive approximation in targeted movement: An alternative hypothesis.Paul J. Cordo & Leslie Bevan - 1992 - Behavioral and Brain Sciences 15 (4):729-730.
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