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Dive into the research topics where Anthony R. Dickinson is active.

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Featured researches published by Anthony R. Dickinson.


Nature Neuroscience | 2002

Non-spatial, motor-specific activation in posterior parietal cortex

Jeffrey L. Calton; Anthony R. Dickinson; Lawrence H. Snyder

A localized cluster of neurons in macaque posterior parietal cortex, termed the parietal reach region (PRR), is activated when a reach is planned to a visible or remembered target. To explore the role of PRR in sensorimotor transformations, we tested whether cells would be activated when a reach is planned to an as-yet unspecified goal. Over one-third of PRR cells increased their firing after an instruction to prepare a reach, but not after an instruction to prepare a saccade, when the target of the movement remained unknown. A partially overlapping population (two-thirds of cells) was activated when the monkey was informed of the target location but not the type of movement to be made. Thus a subset of PRR neurons separately code spatial and effector-specific information, consistent with a role in specifying potential motor responses to particular targets.


The Journal of Neuroscience | 2008

Limb-Specific Representation for Reaching in the Posterior Parietal Cortex

Steve W. C. Chang; Anthony R. Dickinson; Lawrence H. Snyder

To reach for something we see, the brain must integrate the target location with the limb to be used for reaching. Neuronal activity in the parietal reach region (PRR) located in the posterior parietal cortex represents targets for reaching. Does this representation depend on the limb to be used? We found a continuum of limb-dependent and limb-independent responses: some neurons represented targets for movements of either limb, whereas others represented only contralateral-limb targets. Only a few cells represented ipsilateral-limb targets. Furthermore, these representations were not dependent on preferred direction. Additional experiments provide evidence that the PRR is specifically involved in contralateral-limb movements: firing rates are correlated with contralateral- but not ipsilateral-limb reaction times. The current study therefore provides novel evidence that the PRR operates as a limb-dependent stage that lies further along the sensory–motor transformation for visually guided reaching than previously expected.


The Journal of Neuroscience | 2006

Preparatory Delay Activity in the Monkey Parietal Reach Region Predicts Reach Reaction Times

Lawrence H. Snyder; Anthony R. Dickinson; Jeffrey L. Calton

To acquire something that we see, visual spatial information must ultimately result in the activation of the appropriate set of muscles. This sensory to motor transformation requires an interaction between information coding target location and information coding which effector will be moved. Activity in the monkey parietal reach region (PRR) reflects both spatial information and the effector (arm or eye) that will be used in an upcoming reach or saccade task. To further elucidate the functional role of PRR in visually guided movement tasks and to obtain evidence that PRR signals are used to drive arm movements, we tested the hypothesis that increased neuronal activity during a preparatory delay period would lead to faster reach reaction times but would not be correlated with saccade reaction times. This proved to be the case only when the type of movement and not the spatial goal of that movement was known in advance. The correlation was strongest in cells that showed significantly more activity on arm reach compared with saccade trials. No significant correlations were found during delay periods in which spatial information was provided in advance. These data support the idea that PRR constitutes a bottleneck in the processing of spatial information for an upcoming arm reach. The lack of a correlation with saccadic reaction time also supports the idea that PRR processing is effector specific, that is, it is involved in specifying targets for arm movements but not targets for eye movements.


Cerebral Cortex | 2016

Region-Specific Summation Patterns Inform the Role of Cortical Areas in Selecting Motor Plans

Steve W. C. Chang; Jeffrey L. Calton; Bonnie M. Lawrence; Anthony R. Dickinson; Lawrence H. Snyder

Given an instruction regarding which effector to move and what location to move to, simply adding the effector and spatial signals together will not lead to movement selection. For this, a nonlinearity is required. Thresholds, for example, can be used to select a particular response and reject others. Here we consider another useful nonlinearity, a supralinear multiplicative interaction. To help select a motor plan, spatial and effector signals could multiply and thereby amplify each other. Such an amplification could constitute one step within a distributed network involved in response selection, effectively boosting one response while suppressing others. We therefore asked whether effector and spatial signals sum supralinearly for planning eye versus arm movements from the parietal reach region (PRR), the lateral intraparietal area (LIP), the frontal eye field (FEF), and a portion of area 5 (A5) lying just anterior to PRR. Unlike LIP neurons, PRR, FEF, and, to a lesser extent, A5 neurons show a supralinear interaction. Our results suggest that selecting visually guided eye versus arm movements is likely to be mediated by PRR and FEF but not LIP.


Journal of Neurophysiology | 2002

Eye-hand coordination: saccades are faster when accompanied by a coordinated arm movement.

Lawrence H. Snyder; Jeffrey L. Calton; Anthony R. Dickinson; Bonnie M. Lawrence


Journal of Neurophysiology | 2003

Nonspatial Saccade-Specific Activation in area LIP of Monkey Parietal Cortex

Anthony R. Dickinson; Jeffrey L. Calton; Lawrence H. Snyder


Archive | 2015

Contralateral Versus Ipsilateral Arm Premotor Cortex In Reaching Tasks With the Neural Activity in Primary Motor and Dorsal

Donald J. Crammond; John F. Kalaska; Jason P. Gallivan; Ingrid S. Johnsrude; J. Randall Flanagan; Lawrence H. Snyder; Steve W. C. Chang; Jeffrey L. Calton; Bonnie M. Lawrence; Anthony R. Dickinson; Yoshihisa Nakayama; Osamu Yokoyama; Eiji Hoshi


Archive | 2015

Programming in Macaque Frontal Eye Field Dissociation of Visual Discrimination From Saccade

Narcisse P. Bichot; Jeffrey D. Schall; Hugo L. Fernandes; Ian H. Stevenson; Adam N. Phillips; Mark A. Segraves; Nicholas E. DiQuattro; Risa Sawaki; Joy J. Geng; H. Snyder; Steve W. C. Chang; Jeffrey L. Calton; Bonnie M. Lawrence; Anthony R. Dickinson; Natalie Caspari; Thomas Janssens; Dante Mantini; Rik Vandenberghe; Wim Vanduffel


Archive | 2015

ActionPosterior Parietal Cortex for the Planning of Integration of Target and Effector Information in

Herbert C. Goltz; J. Douglas Crawford; Tutis Vilis; Tianxia Wu; Han Wang; Mark Hallett; Chi-Chao Chao; Rainer Paine; Ana Carolina de Campos; Elsie Premereur; Peter Janssen; Wim Vanduffel; Lawrence H. Snyder; Steve W. C. Chang; Jeffrey L. Calton; Bonnie M. Lawrence; Anthony R. Dickinson


Archive | 2014

dorsal parietofrontal cortex Effector selection precedes reach planning in the

Matthew Cieslak; Scott T. Grafton; Eric A. Yttri; Cunguo Wang; Yuqing Liu; Lawrence H. Snyder; Steve W. C. Chang; Jeffrey L. Calton; Bonnie M. Lawrence; Anthony R. Dickinson

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Jeffrey L. Calton

California State University

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Lawrence H. Snyder

Washington University in St. Louis

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Wim Vanduffel

Katholieke Universiteit Leuven

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Elsie Premereur

Katholieke Universiteit Leuven

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Peter Janssen

Katholieke Universiteit Leuven

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Cunguo Wang

Washington University in St. Louis

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