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  1. The representing brain: Neural correlates of motor intention and imagery.Marc Jeannerod - 1994 - Behavioral and Brain Sciences 17 (2):187-202.
    This paper concerns how motor actions are neurally represented and coded. Action planning and motor preparation can be studied using a specific type of representational activity, motor imagery. A close functional equivalence between motor imagery and motor preparation is suggested by the positive effects of imagining movements on motor learning, the similarity between the neural structures involved, and the similar physiological correlates observed in both imaging and preparing. The content of motor representations can be inferred from motor images at a (...)
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  • The dynamical hypothesis in cognitive science.Tim van Gelder - 1998 - Behavioral and Brain Sciences 21 (5):615-28.
    According to the dominant computational approach in cognitive science, cognitive agents are digital computers; according to the alternative approach, they are dynamical systems. This target article attempts to articulate and support the dynamical hypothesis. The dynamical hypothesis has two major components: the nature hypothesis (cognitive agents are dynamical systems) and the knowledge hypothesis (cognitive agents can be understood dynamically). A wide range of objections to this hypothesis can be rebutted. The conclusion is that cognitive systems may well be dynamical systems, (...)
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  • Strategies for the control of voluntary movements with one mechanical degree of freedom.Gerald L. Gottlieb, Daniel M. Corcos & Gyan C. Agarwal - 1989 - Behavioral and Brain Sciences 12 (2):189-210.
    A theory is presented to explain how accurate, single-joint movements are controlled. The theory applies to movements across different distances, with different inertial loads, toward targets of different widths over a wide range of experimentally manipulated velocities. The theory is based on three propositions. (1) Movements are planned according to “strategies” of which there are at least two: a speed-insensitive (SI) and a speed-sensitive (SS) one. (2) These strategies can be equated with sets of rules for performing diverse movement tasks. (...)
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  • The dynamics of embodiment: A field theory of infant perseverative reaching.Esther Thelen, Gregor Schöner, Christian Scheier & Linda B. Smith - 2001 - Behavioral and Brain Sciences 24 (1):1-34.
    The overall goal of this target article is to demonstrate a mechanism for an embodied cognition. The particular vehicle is a much-studied, but still widely debated phenomenon seen in 7–12 month-old-infants. In Piaget's classic “A-not-B error,” infants who have successfully uncovered a toy at location “A” continue to reach to that location even after they watch the toy hidden in a nearby location “B.” Here, we question the traditional explanations of the error as an indicator of infants' concepts of objects (...)
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  • For effective sensorimotor processing must there be explicit representations and reconciliation of differing frames of reference?Garrett E. Alexander - 1992 - Behavioral and Brain Sciences 15 (2):321-322.
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  • Homing in on consciousness in the nervous system: An action-based synthesis.Ezequiel Morsella, Christine A. Godwin, Tiffany K. Jantz, Stephen C. Krieger & Adam Gazzaley - 2016 - Behavioral and Brain Sciences 39:1-70.
    What is the primary function of consciousness in the nervous system? The answer to this question remains enigmatic, not so much because of a lack of relevant data, but because of the lack of a conceptual framework with which to interpret the data. To this end, we have developed Passive Frame Theory, an internally coherent framework that, from an action-based perspective, synthesizes empirically supported hypotheses from diverse fields of investigation. The theory proposes that the primary function of consciousness is well-circumscribed, (...)
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  • Coordinate transformation and limb movements: There may be more complexity than meets the eye.James R. Bloedel - 1992 - Behavioral and Brain Sciences 15 (2):326-326.
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  • The link between brain learning, attention, and consciousness.Stephen Grossberg - 1999 - Consciousness and Cognition 8 (1):1-44.
    The processes whereby our brains continue to learn about a changing world in a stable fashion throughout life are proposed to lead to conscious experiences. These processes include the learning of top-down expectations, the matching of these expectations against bottom-up data, the focusing of attention upon the expected clusters of information, and the development of resonant states between bottom-up and top-down processes as they reach an attentive consensus between what is expected and what is there in the outside world. It (...)
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  • Early stages in a sensorimotor transformation.Martha Flanders, Stephen I. Helms Tillery & John F. Soechting - 1992 - Behavioral and Brain Sciences 15 (2):309-320.
    We present a model for several early stages of the sensorimotor transformations involved in targeted arm movement. In psychophysical experiments, human subjects pointed to the remembered locations of randomly placed targets in three-dimensional space. They made consistent errors in distance, and from these errors stages in the sensorimotor transformation were deduced. When subjects attempted to move the right index finger to a virtual target they consistently undershot the distance of the more distal targets. Other experiments indicated that the error was (...)
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  • The origin and use of positional frames of reference in motor control.Anatol G. Feldman & Mindy F. Levin - 1995 - Behavioral and Brain Sciences 18 (4):723-744.
    A hypothesis about sensorimotor integration (the λ model) is described and applied to movement control and kinesthesia. The central idea is that the nervous system organizes positional frames of reference for the sensorimotor apparatus and produces active movements by shifting the frames in terms of spatial coordinates. Kinematic and electromyographic patterns are not programmed, but emerge from the dynamic interaction among the system s components, including external forces within the designated frame of reference. Motoneuronal threshold properties and proprioceptive inputs to (...)
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  • The quest for optimality: A positive heuristic of science?Paul J. H. Schoemaker - 1991 - Behavioral and Brain Sciences 14 (2):205-215.
    This paper examines the strengths and weaknesses of one of science's most pervasive and flexible metaprinciples;optimalityis used to explain utility maximization in economics, least effort principles in physics, entropy in chemistry, and survival of the fittest in biology. Fermat's principle of least time involves both teleological and causal considerations, two distinct modes of explanation resting on poorly understood psychological primitives. The rationality heuristic in economics provides an example from social science of the potential biases arising from the extreme flexibility of (...)
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  • Kinesthesia and unique solutions for control of multijoint movements.S. C. Gandevia - 1992 - Behavioral and Brain Sciences 15 (2):335-335.
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  • Are errors in final position destined before the movement begins?Z. Hasan - 1992 - Behavioral and Brain Sciences 15 (2):341-342.
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  • Strategies for the control of studies of voluntary movements with one mechanical degree of freedom.Gerale E. Loeb - 1989 - Behavioral and Brain Sciences 12 (2):227-227.
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  • Coordinate transformations or dynamic models?Peter D. Neilson - 1992 - Behavioral and Brain Sciences 15 (2):348-348.
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  • Jeannerod's representing brain: Image or illusion?Jean Pailhous & Mireille Bonnard - 1994 - Behavioral and Brain Sciences 17 (2):215-216.
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  • Dynamic field theory of movement preparation.Wolfram Erlhagen & Gregor Schöner - 2002 - Psychological Review 109 (3):545-572.
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  • Speech sound acquisition, coarticulation, and rate effects in a neural network model of speech production.Frank H. Guenther - 1995 - Psychological Review 102 (3):594-621.
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  • Posture-based motion planning: Applications to grasping.David A. Rosenbaum, Ruud J. Meulenbroek, Jonathan Vaughan & Chris Jansen - 2001 - Psychological Review 108 (4):709-734.
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  • Planning reaches by evaluating stored postures.David A. Rosenbaum, Loukia D. Loukopoulos, Ruud G. J. Meulenbroek, Jonathan Vaughan & Sascha E. Engelbrecht - 1995 - Psychological Review 102 (1):28-67.
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  • The prerequisites for one-jint motor control theories.S. V. Adamovich & A. G. Feldman - 1989 - Behavioral and Brain Sciences 12 (2):210-211.
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  • Direct pattern-imposing control or dynamic regulation?Marl L. Latash - 1989 - Behavioral and Brain Sciences 12 (2):226-227.
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  • Braking may be more critical than acceleration.William A. MacKay - 1989 - Behavioral and Brain Sciences 12 (2):227-228.
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  • Nonconscious motor images.Giacomo Rizzolatti - 1994 - Behavioral and Brain Sciences 17 (2):220-220.
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  • Call it what it is: Motor memory.Joaquin M. Fuster - 1994 - Behavioral and Brain Sciences 17 (2):208-208.
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  • Action and attention.A. H. C. Van der Heijden & Bruce Bridgeman - 1994 - Behavioral and Brain Sciences 17 (2):225-226.
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  • On the relation between motor imagery and visual imagery.Roberta L. Klatzky - 1994 - Behavioral and Brain Sciences 17 (2):212-213.
    Jeannerod's target article describes support, through empirical and neurological findings, for the intriguing idea of motor imagery, a form of representation hypothesized to have levels of functional equivalence with motor preparation, while being consciously accessible. Jeannerod suggests that the subjectively accessible content of motor imagery allows it to be distinguished from motor preparation, which is unconscious. Motor imagery is distinguished from visual imagery in terms of content. Motor images are kinesthetic in nature; they are parametrized by variables such as force (...)
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  • Motor representations and reality.M. Jeannerod - 1994 - Behavioral and Brain Sciences 17 (2):229-245.
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  • Moving beyond imagination.Robert Dufour, Martin H. Fischer & David A. Rosenbaum - 1994 - Behavioral and Brain Sciences 17 (2):206-207.
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  • Motor memory – a memory of the future.David H. Ingvar - 1994 - Behavioral and Brain Sciences 17 (2):210-211.
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  • Are motor images based on kinestheticvisual matching?Robert W. Mitchell - 1994 - Behavioral and Brain Sciences 17 (2):214-215.
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  • Separability of reference frame distinctions from motor and visual images.Gary W. Strong - 1994 - Behavioral and Brain Sciences 17 (2):224-225.
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  • Cognitive and motor implications of mental imagery.Romeo Chua & Daniel J. Weeks - 1994 - Behavioral and Brain Sciences 17 (2):203-204.
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  • Visual-spatial movement goals.Digby Elliott & Brian K. V. Maraj - 1994 - Behavioral and Brain Sciences 17 (2):207-207.
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  • Motor images are action plans.Wolfgang Prinz - 1994 - Behavioral and Brain Sciences 17 (2):218-218.
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  • Stopping eyes and hands: evidence for non-independence of stop and go processes and for a separation of central and peripheral inhibition.Alessandro Gulberti, Petra A. Arndt & Hans Colonius - 2014 - Frontiers in Human Neuroscience 8.
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  • The infinite regress of optimization.Philippe Mongin - 1991 - Behavioral and Brain Sciences 14 (2):229-230.
    A comment on Paul Schoemaker's target article in Behavioral and Brain Sciences, 14 (1991), p. 205-215, "The Quest for Optimality: A Positive Heuristic of Science?" (https://doi.org/10.1017/S0140525X00066140). This comment argues that the optimizing model of decision leads to an infinite regress, once internal costs of decision (i.e., information and computation costs) are duly taken into account.
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  • Physical modeling applies to physiology, too.Vincent Hayward - 1992 - Behavioral and Brain Sciences 15 (2):342-343.
    A physical model was utilized to show that the neural system can memorize a target position and is able to cause motor and sensory events that move the arm to a target with more accuracy. However, this cannot indicate in which coordinates the necessary computations are carried out. Turning off the lights causes the error to increase which is accomplished by cutting off one feedback path. The geometrical properties of arm kinematics and the properties of the kinesthetic and visual sensorial (...)
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  • Motor simulation.Adam Morton - 1994 - Behavioral and Brain Sciences 17 (2):215-215.
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  • Involvement of primary motor cortex in motor imagery and mental practice.Mark Hallett, Jordan Fieldman, Leonardo G. Cohen, Norihiro Sadato & Alvaro Pascual-Leone - 1994 - Behavioral and Brain Sciences 17 (2):210-210.
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  • The strategy of optimality revisited.Paul J. H. Schoemaker - 1991 - Behavioral and Brain Sciences 14 (2):237-245.
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  • Extremum descriptions, process laws and minimality heuristics.Elliott Sober - 1991 - Behavioral and Brain Sciences 14 (2):232-233.
    The examples and concepts that Shoemaker cites are rather heterogeneous. Some distinctions need to be drawn. An optimality thesis involves not just an ordering of options, but a value judgment about them. So let us begin by distinguishing minimality from optimality. And the concept of minimality can play a variety of roles, among which I distinguish between extremum descriptions, statements hypothesizing an optimizing process, and methodological recommendations. Finally, I consider how the three categories relate to Shoemaker’s question that “Who is (...)
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  • Should the quest for optimality worry us?Nils-Eric Sahlin - 1991 - Behavioral and Brain Sciences 14 (2):231-231.
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  • Is the multi-joint pointing movement model applicable to equilibrium control during upper trunk movements?Alexey Alexandrov, Alexander Frolov & Jean Massion - 1995 - Behavioral and Brain Sciences 18 (4):745-746.
    Two aspects of the target article, (1) the extension of the equilibrium point theory to multi-joint movements, and (2) the consequence that the EMG pattern is not directly controlled by the central nervous system (CNS), are discussed in light of the experiments on upper trunk bending in humans. The principle component kinematic analysis and the analysis of the EMG data, obtained under microgravity and additional loading conditions, support the application of Feldman and Levin's for multi-joint pointing movement to equilibrium control (...)
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  • Tendon elasticity and positional control.R. McN Alexander - 1995 - Behavioral and Brain Sciences 18 (4):745-745.
    The spring-like behaviour of a joint following a sudden change of torque is partly a result of the elastic properties of tendons. A large fall in a muscle with a long tendon may be accompanied by tendon recoil causing joint movements as large as 20°.
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  • Contiguity, contingency, and causation.R. J. Andrew - 1988 - Behavioral and Brain Sciences 11 (3):447.
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  • Optimality and human memory.John R. Anderson - 1991 - Behavioral and Brain Sciences 14 (2):215-216.
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  • Schemas, grasping, tensors and avoidance.Michael A. Arbib - 1992 - Behavioral and Brain Sciences 15 (2):322-323.
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  • Do object affordances represent the functionality of an object?Ruzena Bajcsy - 1994 - Behavioral and Brain Sciences 17 (2):202-202.
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  • Optimality as an evaluative standard in the study of decision-making.Jonathan Baron - 1991 - Behavioral and Brain Sciences 14 (2):216-216.
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