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      Consensus Paper: The Role of the Cerebellum in Perceptual Processes

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          Abstract

          Various lines of evidence accumulated over the past 30 years indicate that the cerebellum, long recognized as essential for motor control, also has considerable influence on perceptual processes. In this paper, we bring together experts from psychology and neuroscience, with the aim of providing a succinct but comprehensive overview of key findings related to the involvement of the cerebellum in sensory perception. The contributions cover such topics as anatomical and functional connectivity, evolutionary and comparative perspectives, visual and auditory processing, biological motion perception, nociception, self-motion, timing, predictive processing, and perceptual sequencing. While no single explanation has yet emerged concerning the role of the cerebellum in perceptual processes, this consensus paper summarizes the impressive empirical evidence on this problem and highlights diversities as well as commonalities between existing hypotheses. In addition to work with healthy individuals and patients with cerebellar disorders, it is also apparent that several neurological conditions in which perceptual disturbances occur, including autism and schizophrenia, are associated with cerebellar pathology. A better understanding of the involvement of the cerebellum in perceptual processes will thus likely be important for identifying and treating perceptual deficits that may at present go unnoticed and untreated. This paper provides a useful framework for further debate and empirical investigations into the influence of the cerebellum on sensory perception.

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          Bayesian integration in sensorimotor learning.

          When we learn a new motor skill, such as playing an approaching tennis ball, both our sensors and the task possess variability. Our sensors provide imperfect information about the ball's velocity, so we can only estimate it. Combining information from multiple modalities can reduce the error in this estimate. On a longer time scale, not all velocities are a priori equally probable, and over the course of a match there will be a probability distribution of velocities. According to bayesian theory, an optimal estimate results from combining information about the distribution of velocities-the prior-with evidence from sensory feedback. As uncertainty increases, when playing in fog or at dusk, the system should increasingly rely on prior knowledge. To use a bayesian strategy, the brain would need to represent the prior distribution and the level of uncertainty in the sensory feedback. Here we control the statistical variations of a new sensorimotor task and manipulate the uncertainty of the sensory feedback. We show that subjects internally represent both the statistical distribution of the task and their sensory uncertainty, combining them in a manner consistent with a performance-optimizing bayesian process. The central nervous system therefore employs probabilistic models during sensorimotor learning.
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            Evidence for topographic organization in the cerebellum of motor control versus cognitive and affective processing.

            Patients with cerebellar damage often present with the cerebellar motor syndrome of dysmetria, dysarthria and ataxia, yet cerebellar lesions can also result in the cerebellar cognitive affective syndrome (CCAS), including executive, visual spatial, and linguistic impairments, and affective dysregulation. We have hypothesized that there is topographic organization in the human cerebellum such that the anterior lobe and lobule VIII contain the representation of the sensorimotor cerebellum; lobules VI and VII of the posterior lobe comprise the cognitive cerebellum; and the posterior vermis is the anatomical substrate of the limbic cerebellum. Here we analyze anatomical, functional neuroimaging, and clinical data to test this hypothesis. We find converging lines of evidence supporting regional organization of motor, cognitive, and limbic behaviors in the cerebellum. The cerebellar motor syndrome results when lesions involve the anterior lobe and parts of lobule VI, interrupting cerebellar communication with cerebral and spinal motor systems. Cognitive impairments occur when posterior lobe lesions affect lobules VI and VII (including Crus I, Crus II, and lobule VIIB), disrupting cerebellar modulation of cognitive loops with cerebral association cortices. Neuropsychiatric disorders manifest when vermis lesions deprive cerebro-cerebellar-limbic loops of cerebellar input. We consider this functional topography to be a consequence of the differential arrangement of connections of the cerebellum with the spinal cord, brainstem, and cerebral hemispheres, reflecting cerebellar incorporation into the distributed neural circuits subserving movement, cognition, and emotion. These observations provide testable hypotheses for future investigations. Copyright (c) 2009 Elsevier Srl. All rights reserved.
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              Life at low Reynolds number

              E. Purcell (1977)
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                Author and article information

                Contributors
                o.baumann@uq.edu.au
                Journal
                Cerebellum
                Cerebellum
                Cerebellum (London, England)
                Springer US (Boston )
                1473-4222
                1473-4230
                6 December 2014
                6 December 2014
                2015
                : 14
                : 2
                : 197-220
                Affiliations
                [ ]Queensland Brain Institute, The University of Queensland, St. Lucia, Queensland Australia
                [ ]Department of Radiology and Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA USA
                [ ]Department of Diagnostic Radiology, Medical Imaging Centre of Southwest Finland, Turku University Hospital, Turku, Finland
                [ ]Numedon Inc., Pasadena, CA USA
                [ ]Department of Physiology, McGill University Montreal, Montreal, Canada
                [ ]Service de NeuroImagerie, CHNO des Quinze-Vingts, UPMC Paris 6, Paris, France
                [ ]Department of Psychology, University of California, Berkeley, CA USA
                [ ]Department of Psychology, Sapienza University of Rome, Rome, Italy
                [ ]I.R.C.C.S. Santa Lucia Foundation, Rome, Italy
                [ ]Pain/Analgesia Imaging Neuroscience (P.A.I.N.) Group, Department of Anesthesia, Boston Children’s Hospital, Center for Pain and the Brain, Harvard Medical School, Waltham, MA USA
                [ ]Department of Zoology, University of Otago, Otago, New Zealand
                [ ]Department of Biomedical Magnetic Resonance, Medical School, Eberhard Karls University of Tübingen, Tübingen, Germany
                [ ]Ataxia Unit, Cognitive Behavioral Neurology Unit, Laboratory for Neuroanatomy and Cerebellar Neurobiology Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA USA
                [ ]Département des Neurosciences Cliniques, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland
                Article
                627
                10.1007/s12311-014-0627-7
                4346664
                25479821
                68e6e50c-b77f-41e5-a5d7-625625c87e89
                © The Author(s) 2014

                Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

                History
                Categories
                Consensus Paper
                Custom metadata
                © Springer Science+Business Media New York 2015

                Neurology
                audition,biological motion,cerebellum,connectivity,evolution,fmri,pain,perception,prediction,single-unit recording,self-motion,sequencing,state estimation,timing,vision

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