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      New Light on the Mind’s Eye : The Pupillary Light Response as Active Vision

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          Abstract

          The eye’s pupils constrict (shrink) in brightness and dilate (expand) in darkness. The pupillary light response was historically considered a low-level reflex without any cognitive component. Here, we review recent studies that have dramatically changed this view: The light response depends not only on a stimulus’s brightness but also on whether you are aware of the stimulus, whether you are paying attention to it, and even whether you are thinking about it. We highlight the link between the pupillary light response and eye-movement preparation: When you intend to look at a bright stimulus, a pupillary constriction is prepared along with the eye movement before the eyes set in motion. This preparation allows the pupil to rapidly change its size as your eyes move from bright to dark objects and back again. We discuss the implications of these recent advances for our understanding of the subtle yet important role that pupillary responses play in vision.

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          Most cited references25

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          An integrative theory of locus coeruleus-norepinephrine function: adaptive gain and optimal performance.

          Historically, the locus coeruleus-norepinephrine (LC-NE) system has been implicated in arousal, but recent findings suggest that this system plays a more complex and specific role in the control of behavior than investigators previously thought. We review neurophysiological and modeling studies in monkey that support a new theory of LC-NE function. LC neurons exhibit two modes of activity, phasic and tonic. Phasic LC activation is driven by the outcome of task-related decision processes and is proposed to facilitate ensuing behaviors and to help optimize task performance (exploitation). When utility in the task wanes, LC neurons exhibit a tonic activity mode, associated with disengagement from the current task and a search for alternative behaviors (exploration). Monkey LC receives prominent, direct inputs from the anterior cingulate (ACC) and orbitofrontal cortices (OFC), both of which are thought to monitor task-related utility. We propose that these frontal areas produce the above patterns of LC activity to optimize utility on both short and long timescales.
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            Visual attention: the past 25 years.

            This review focuses on covert attention and how it alters early vision. I explain why attention is considered a selective process, the constructs of covert attention, spatial endogenous and exogenous attention, and feature-based attention. I explain how in the last 25 years research on attention has characterized the effects of covert attention on spatial filters and how attention influences the selection of stimuli of interest. This review includes the effects of spatial attention on discriminability and appearance in tasks mediated by contrast sensitivity and spatial resolution; the effects of feature-based attention on basic visual processes, and a comparison of the effects of spatial and feature-based attention. The emphasis of this review is on psychophysical studies, but relevant electrophysiological and neuroimaging studies and models regarding how and where neuronal responses are modulated are also discussed. Copyright © 2011 Elsevier Ltd. All rights reserved.
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              Task-evoked pupillary responses, processing load, and the structure of processing resources.

              J Beatty (1982)
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                Author and article information

                Journal
                Curr Dir Psychol Sci
                Curr Dir Psychol Sci
                CDP
                spcdp
                Current Directions in Psychological Science
                SAGE Publications (Sage CA: Los Angeles, CA )
                0963-7214
                1467-8721
                October 2015
                October 2015
                : 24
                : 5
                : 374-378
                Affiliations
                [1 ]Laboratoire de Psychologie Cognitive, CNRS, Aix-Marseille University, Marseille, France
                [2 ]Department of Experimental Psychology, Helmholtz Institute, Utrecht University
                Author notes
                [*]Sebastiaan Mathôt, Aix-Marseille University, CNRS, Laboratoire de Psychologie Cognitive, UMR 7290, 3 Place Victor Hugo, Centre St. Charles, Bâtiment 9, Case D, 13331 Marseille, France E-mail: s.mathot@ 123456cogsci.nl
                Article
                10.1177_0963721415593725
                10.1177/0963721415593725
                4601080
                26494950
                8bd987f9-cac9-4400-8ac4-5eb186fdc071
                © The Author(s) 2015

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License ( http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

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                Categories
                Article

                Clinical Psychology & Psychiatry
                pupil size,eye movements,visual perception,arousal
                Clinical Psychology & Psychiatry
                pupil size, eye movements, visual perception, arousal

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