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  1. The Necessity of Ambiguity in Self–Other Processing: A Psychosocial Perspective With Implications for Mental Health.Christophe Emmanuel de Bézenac, Rachel Ann Swindells & Rhiannon Corcoran - 2018 - Frontiers in Psychology 9.
    While distinguishing between the actions and physical boundaries of self and other (non-self) is usually straightforward there are contexts in which such differentiation is challenging. For example, self-other ambiguity may occur when actions of others are similar or complementary to those of the self. Even in the absence of such situational challenges, individuals experiencing hallucinations have difficulties with this distinction, often experiencing thoughts or actions of self as belonging to other agents. This paper explores the role of ambiguity in self-other (...)
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  • The lambda model is only one piece in the motor control puzzle.Jeffrey Dean - 1995 - Behavioral and Brain Sciences 18 (4):749-749.
    The lambda model provides a physiologically grounded terminology for describing muscle function and emphasizes the important influence of environmental and reflex-mediated effects on final states. However, lambda itself is only a convenient point on the length-tension curve; its importance should not be overemphasized. Ascribing movement to changes in a lambda-based frame of reference is generally valid, but it leaves unanswered a number of questions concerning mechanisms.
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  • Temporal representation in the control of movement.Daniel M. Corcos - 1994 - Behavioral and Brain Sciences 17 (2):206-206.
    Theories of the representation of specific kinetic and spatiotem-poral features of movement range from the explicit assertion that temporal aspects of movement are not represented to the idea that they are represented and that they have neurophysiological correlates. Jeannerod's thesis is that mental and visual images have common mechanisms and that there is a link between the image to move and the mechanisms involved with movement. The target article takes the position that certain parameters are coded in motor representations but (...)
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  • Conservative or nonconservative control schemes.Daniel M. Corcos & Kerstin Pfann - 1995 - Behavioral and Brain Sciences 18 (4):747-749.
    The conservative strategy proposed by the authors suggests a solution of the degrees-of-freedom problem of the controller. However, several simple motor control tasks cannot be explained by this strategy. A nonconservative strategy, in which more parameters of the control signal vary, can account for these simple motor tasks. However, the simplicity that distinguishes the proposed model from many others is lost.
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  • The creative brain: Symmetry breaking in motor imagery.José L. Contreras-Vidal, Jean P. Banquet, Jany Brebion & Mark J. Smith - 1994 - Behavioral and Brain Sciences 17 (2):204-205.
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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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  • Dissociation between dreams and wakefulness: Insights from body and action representations of rare individuals with massive somatosensory deafferentation.Ishan-Singh J. Chauhan, Jonathan D. Cole, Alain Berthoz & Fabrice R. Sarlegna - 2022 - Consciousness and Cognition 106 (C):103415.
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  • On the limitations of imaging imagining.Christopher A. Buneo & Martha Flanders - 1994 - Behavioral and Brain Sciences 17 (2):202-203.
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  • Interdiscourse or supervenience relations: The primacy of the manifest image.J. Brakel - 1996 - Synthese 106 (2):253 - 297.
    Amidst the progress being made in the various (sub-)disciplines of the behavioural and brain sciences a somewhat neglected subject is the problem of how everything fits into one world and, derivatively, how the relation between different levels of discourse should be understood and to what extent different levels, domains, approaches, or disciplines are autonomous or dependent. In this paper I critically review the most recent proposals to specify the nature of interdiscourse relations, focusing on the concept of supervenience. Ideally supervenience (...)
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  • A few reasons why psychologlsts can adhere to Feldman and Levin's model.Mireille Bonnard & Jean Pailhous - 1995 - Behavioral and Brain Sciences 18 (4):746-747.
    We emphasize the relevance to cognitive psychology of Feldman and Levin's theoretical position. Traditional views of motor control have failed to clearly separate “production control” at the level of motor command, based on task-independent CV (control variables), from intentional “product control” based on task-dependent parameters. Because F&L's approach concentrates on the first process (trajectory formation), it can distinguish the product control stage.
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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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  • 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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  • 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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  • On the inference of personal authorship: Enhancing experienced agency by priming effect information☆.Henk Aarts, Ruud Custers & Daniel M. Wegner - 2005 - Consciousness and Cognition 14 (3):439-458.
    Three experiments examined whether the mere priming of potential action effects enhances people’s feeling of causing these effects when they occur. In a computer task, participants and the computer independently moved a rapidly moving square on a display. Participants had to press a key, thereby stopping the movement. However, the participant or the computer could have caused the square to stop on the observed position, and accordingly, the stopped position of the square could be conceived of as the potential effect (...)
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  • A False Trail to Follow: Differential Effects of the Facial Feedback Signals From the Upper and Lower Face on the Recognition of Micro-Expressions.Xuemei Zeng, Qi Wu, Siwei Zhang, Zheying Liu, Qing Zhou & Meishan Zhang - 2018 - Frontiers in Psychology 9:411700.
    Micro-expressions, as fleeting facial expressions, are very important for judging people’s true emotions, thus can provide an essential behavioral clue for lie and dangerous demeanor detection. From embodied accounts of cognition, we derived a novel hypothesis that facial feedback from upper and lower facial regions has differential effects on micro-expression recognition. This hypothesis was tested and supported across three studies. Specifically, the results of Study 1 showed that people became better judges of intense micro-expressions with a duration of 450 ms (...)
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  • Biological variability and control of movements via δλ.Charles E. Wright & Rebecca A. States - 1995 - Behavioral and Brain Sciences 18 (4):786-786.
    Three issues related to Feldman and Levin's treatment of biological variability are discussed. We question the usefulness of the indirect component of δλ. We suggest that trade-offs between speed and accuracy in aimed movements support identification of δλ, rather than λ, as a control variable. We take issue with the authors' proposal for resolving redundancy in multi-joint movements, given recent data.
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  • Levers to generate movement.U. Windhorst - 1995 - Behavioral and Brain Sciences 18 (4):784-785.
    The following questions are discussed: (1) Who determines the nature of “control variables”? (2) Is the “positional monopoly” healthy? (3) Does a descending command alter reflex threshold alone without eoncomitantly altering stiffness? (4) How does the CNS deal with history-dependent effects? (5) Should we abandon the idea that the CNS controls classical Newtonian variables such as muscle length?
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  • How far should we extend the equilibrium point (lambda) hypothesis?Jack M. Winters - 1995 - Behavioral and Brain Sciences 18 (4):785-786.
    A key feature of the lambda model is the hypothesis of a local spring-like muscle-reflex system defined by a central control variable that has units of position. This is intriguing, especially for a study of postural stability in large-scale systems, but it has limited direct application to skilled everyday movements. If movement is considered as a goal-directed, neuro-optimization problem, however, theavailabilityof lambda-like peripheral models (vs. conventional musculoskeletal models) deserves exploration.
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  • The mystery-mastery-imagery complex.H. T. A. Whiting & R. P. Ingvaldsen - 1994 - Behavioral and Brain Sciences 17 (2):228-229.
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  • Singular Clues to Causality and Their Use in Human Causal Judgment.Peter A. White - 2014 - Cognitive Science 38 (1):38-75.
    It is argued that causal understanding originates in experiences of acting on objects. Such experiences have consistent features that can be used as clues to causal identification and judgment. These are singular clues, meaning that they can be detected in single instances. A catalog of 14 singular clues is proposed. The clues function as heuristics for generating causal judgments under uncertainty and are a pervasive source of bias in causal judgment. More sophisticated clues such as mechanism clues and repeated interventions (...)
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  • Potential disparities between imagining and preparing motor skills.Charles B. Walter & Stephan P. Swinnen - 1994 - Behavioral and Brain Sciences 17 (2):227-228.
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  • Imagery needs preparation too.Stefan Vogt - 1994 - Behavioral and Brain Sciences 17 (2):226-227.
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  • Equifinality and phase-resetting: The role of control parameter manipulations.R. E. A. van Emmerik & R. C. Wagenaar - 1995 - Behavioral and Brain Sciences 18 (4):783-784.
    It is argued that the equilibrium point model can lead to new insights regarding transition and stability processes in movement coordination. The role of movement control parameters on equifinality and phase-resetting is discussed; not only control but also external control parameters can affect the global dynamical regime.
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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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  • Origins of origins of motor control.Esther Thelen - 1995 - Behavioral and Brain Sciences 18 (4):780-783.
    Examination of infant spontaneous and goal-directed arm movements supports Feldman and Levin's hypothesis of a functional hierarchy. Early infant movements are dominated by biomechanical and dynamic factors without external frames of reference. Development involves not only learning to generate these frames of reference, but also protecting the higher-level goal of the movement from internal and external perturbations.
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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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  • Control parameters, equilibria, and coordination dynamics.Dagmar Sternad & M. T. Turvey - 1995 - Behavioral and Brain Sciences 18 (4):780-780.
    Important similarities exist between the dynamical concepts implicit in Feldman & Levin's extended λ model and those basic to a dynamical systems approach. We argue that careful application of the key concepts of control and order parameters, equilibria, and stability, can relate known facts of neuromuscular processes to the observables of functional, task-specific behavior.
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  • Two joints are more than twice one joint.Jeroen B. J. Smeets - 1995 - Behavioral and Brain Sciences 18 (4):779-780.
    An alternative multi-joint extension to the lambda model is proposed. According to this extension, the activity of a muscle depends not only on the difference between lambda and length of that muscle, but also on the difference between lambda and length of other muscles. This 2-D extension can describe more neurophysiological experiments than the extension proposed in the target article.
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  • How do we satisfy our goals?Paul G. Skokowski - 1994 - Behavioral and Brain Sciences 17 (2):224-224.
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  • Canonical representations and constructive praxis: Some developmental and linguistic considerations.Chris Sinha - 1994 - Behavioral and Brain Sciences 17 (2):223-224.
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  • Can the λ model be used to interpret the activity of single neurons?Stephen H. Scott - 1995 - Behavioral and Brain Sciences 18 (4):778-779.
    Whereas the λ model provides a useful technique to describe complex movements, the focus on control variables in this model limits its potential for interpreting the activity and function of many cells in motor areas of the CNS.
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  • Neurophysiology of preparation, movement and imagery.Jerome N. Sanes - 1994 - Behavioral and Brain Sciences 17 (2):221-223.
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  • Kinaesthetic illusions as tools in understanding motor imagery.J. P. Roll, J. C. Gilhodes & R. Roll - 1994 - Behavioral and Brain Sciences 17 (2):220-221.
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  • Nonconscious motor images.Giacomo Rizzolatti - 1994 - Behavioral and Brain Sciences 17 (2):220-220.
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  • To dream is not to (intend to) do.Jean Requin - 1994 - Behavioral and Brain Sciences 17 (2):218-219.
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  • Position is everything?Karl H. Pribram - 1995 - Behavioral and Brain Sciences 18 (4):776-778.
    Neurophysiological evidence consonant with F&L's lambda model is reviewed and results of additional experiments are presented. The evidence shows that there are neurons in the motor cortex that respond to selective band widths of passive sinusoidal movements; the additional data show how, with movement, directionally sensitive population vectors can be shown to emerge from the data.
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  • Motor images are action plans.Wolfgang Prinz - 1994 - Behavioral and Brain Sciences 17 (2):218-218.
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  • Representations of movement and representations in movement.Giuseppe Pellizzer & Apostolos P. Georgopoulos - 1994 - Behavioral and Brain Sciences 17 (2):216-217.
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  • The λ model: Can it walk?Aftab E. Patla - 1995 - Behavioral and Brain Sciences 18 (4):775-776.
    Generation of swing phase limb trajectory over obstacles during locomotion should be a reasonable test for the λ model proposed by Feldman and Levin. The observed features such as lack of simple amplitude scaling of endpoint (toe) trajectories for different obstacle heights, complex shaped toe velocity profiles, and exploitation of passive intersegmental dynamics to control limb elevation cannot be adequately explained by the λ model.
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  • Let us accept a “controlled trade-off” model of motor control.Lloyd D. Partridge - 1995 - Behavioral and Brain Sciences 18 (4):773-775.
    The trade-off between force and length of muscle as adjusted by neural signals is a critical fact in the dynamics of motor control. Whether we call it “length-tension effect,” “feedback-like,” “invariant condition,” or “spring-like” is unimportant. We must not let semantics or details of representation obscure the basic physics of effects introduced by this trade-off in muscle.
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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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  • Spatial frames for motor control would be commensurate with spatial frames for vision and proprioception, but what about control of energy flows?Christopher C. Pagano & Geoffrey P. Bingham - 1995 - Behavioral and Brain Sciences 18 (4):773-773.
    The model identifies a spatial coordinate frame within which the sensorimotor apparatus produces movement. Its spatial nature simplifies its coupling with spatial reference frames used concurrently by vision and proprioception. While the positional reference frame addresses the performance of spatial tasks, it seems to have little to say about movements involving energy expenditure as the principle component of the task.
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  • Command invariants and the frame of reference for human movement.David J. Ostry, Rafael Laboissière & Paul L. Gribble - 1995 - Behavioral and Brain Sciences 18 (4):770-772.
    We describe a solution to the redundancy problem related to that proposed in Feldman & Levin's target article. We suggest that the system may use a fixed mapping between commands organized at the level of degrees of freedom and commands to individual muscles. This proposal eliminates the need to maintain an explicit representation of musculoskeletalgeometry in planning movements.
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  • Interneurons as backseat drivers and the elusive control variable.T. Richard Nichols - 1995 - Behavioral and Brain Sciences 18 (4):772-773.
    It is proposed here that the spinal network of proprioceptive feedback from length and force receptors constitutes the mechanism underlying the coordination of activation thresholds for muscles acting about the same and neighboring joints. For the most part, these circuits come between motoneurons and supraspinal signals, invalidating the idea that the activation thresholds constitute control variables for the motor system.
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  • Motor simulation.Adam Morton - 1994 - Behavioral and Brain Sciences 17 (2):215-215.
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  • Kinematic invariances and body schema.Pietro Morasso & Vittorio Sanguineti - 1995 - Behavioral and Brain Sciences 18 (4):769-770.
    Generalizing the notion that muscles are positional frames of reference, a high-dimensional muscle space is defined for multi-muscle systems with an embedded low-dimensional motor manifold of functional articulators. A central representation of such a manifold is proposed as computational body schema. The example of the jaw-tongue system is presented, discussing the relation of functional articulators with kinematic invariances and control problems.
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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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  • Visually guided action and the “need to know”.A. David Milner, David P. Carey & Monika Harvey - 1994 - Behavioral and Brain Sciences 17 (2):213-214.
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  • Energy, information, detection, and action.Claire F. Michaels & Raoul R. D. Oudejans - 2001 - Behavioral and Brain Sciences 24 (2):230-230.
    Before one can talk about global arrays and multimodal detection, one must be clear about the concept of information: How is it different from energy and how is it detected? And can it come to specify a needed movement? We consider these issues in our commentary.
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  • Can the λ model benefit from understanding human adaptation in weightlessness(and vice versa)?P. Vernon McDonald - 1995 - Behavioral and Brain Sciences 18 (4):768-768.
    Parameters of the lambda model seem tightly linked to certain characteristics of human performance influenced by weightlessness. This commentary suggests that there is a valuable opportunity to probe the lambda model using the changed environment experienced during space flight. The likely benefits are a better model and a better understanding ofthe consequences of weightlessness for human performance.
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