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      Simultaneous recordings of ocular microtremor and microsaccades with a piezoelectric sensor and a video-oculography system

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          Abstract

          Our eyes are in continuous motion. Even when we attempt to fix our gaze, we produce so called “fixational eye movements”, which include microsaccades, drift, and ocular microtremor (OMT). Microsaccades, the largest and fastest type of fixational eye movement, shift the retinal image from several dozen to several hundred photoreceptors and have equivalent physical characteristics to saccades, only on a smaller scale ( Martinez-Conde, Otero-Millan & Macknik, 2013). OMT occurs simultaneously with drift and is the smallest of the fixational eye movements (∼1 photoreceptor width, >0.5 arcmin), with dominant frequencies ranging from 70 Hz to 103 Hz ( Martinez-Conde, Macknik & Hubel, 2004). Due to OMT’s small amplitude and high frequency, the most accurate and stringent way to record it is the piezoelectric transduction method. Thus, OMT studies are far rarer than those focusing on microsaccades or drift. Here we conducted simultaneous recordings of OMT and microsaccades with a piezoelectric device and a commercial infrared video tracking system. We set out to determine whether OMT could help to restore perceptually faded targets during attempted fixation, and we also wondered whether the piezoelectric sensor could affect the characteristics of microsaccades. Our results showed that microsaccades, but not OMT, counteracted perceptual fading. We moreover found that the piezoelectric sensor affected microsaccades in a complex way, and that the oculomotor system adjusted to the stress brought on by the sensor by adjusting the magnitudes of microsaccades.

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          Most cited references50

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          Microsaccades are triggered by low retinal image slip.

          Even during visual fixation of a stationary target, our eyes perform rather erratic miniature movements, which represent a random walk. These "fixational" eye movements counteract perceptual fading, a consequence of fast adaptation of the retinal receptor systems to constant input. The most important contribution to fixational eye movements is produced by microsaccades; however, a specific function of microsaccades only recently has been found. Here we show that the occurrence of microsaccades is correlated with low retinal image slip approximately 200 ms before microsaccade onset. This result suggests that microsaccades are triggered dynamically, in contrast to the current view that microsaccades are randomly distributed in time characterized by their rate-of-occurrence of 1 to 2 per second. As a result of the dynamic triggering mechanism, individual microsaccade rate can be predicted by the fractal dimension of trajectories. Finally, we propose a minimal computational model for the dynamic triggering of microsaccades.
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            A neural mechanism for microsaccade generation in the primate superior colliculus.

            During fixation, the eyes are not still but often exhibit microsaccadic movements. The function of microsaccades is controversial, largely because the neural mechanisms responsible for their generation are unknown. Here, we show that the superior colliculus (SC), a retinotopically organized structure involved in voluntary-saccade target selection, plays a causal role in microsaccade generation. Neurons in the foveal portion of the SC increase their activity before and during microsaccades with sizes of only a few minutes of arc and exhibit selectivity for the direction and amplitude of these movements. Reversible inactivation of these neurons significantly reduces microsaccade rate without otherwise compromising fixation. These results, coupled with computational modeling of SC activity, demonstrate that microsaccades are controlled by the SC and explain the link between microsaccades and visual attention.
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              Saccadic suppression: a review and an analysis.

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                Author and article information

                Contributors
                Journal
                Peerj
                Peerj
                PeerJ
                PeerJ
                PeerJ
                PeerJ Inc. (San Francisco, USA )
                2167-8359
                12 February 2013
                2013
                : 1
                : e14
                Affiliations
                [1 ]Department of Neurobiology , Barrow Neurological Institute, USA
                [2 ]School of Mathematical and Statistical Sciences , Arizona State University, USA
                [3 ]Trinity College Dublin , Dublin 2, Ireland
                [4 ]Department of Signal Theory and Communications , University of Vigo, Spain
                [5 ]Department of Neurosurgery , Barrow Neurological Institute, USA
                [6 ]St. James’s Hospital (Mercer’s Institute for Research in Ageing), Ireland
                [7 ]Unité de Neuroscience , Information et Complexité (CNRS-UNIC), France
                [8 ]St James’s Hospital (Medical Physics and Bioengineering Dept.), Ireland
                [9 ]Department of Neurology , Barrow Neurological Institute, USA
                [10 ]Neuro-Ophthalmology Unit , Barrow Neurological Institute, USA
                [11 ]Neuro-Ophthalmology Consultation: Barnett-Dulaney-Perkins Eye Center , USA
                Article
                14
                10.7717/peerj.14
                3629042
                23638348
                66fb9aad-ec33-41df-8e9a-6b81a6df6f42
                © 2013 McCamy et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 20 November 2012
                : 3 January 2013
                Funding
                Funded by: National Science Foundation
                Award ID: 0643306
                Award ID: 0852636
                Award ID: 1153786
                Award ID: 0726113
                This study was supported by the Barrow Neurological Foundation (awards to SLM and SM-C), the National Science Foundation (awards 0643306, 0852636 and 1153786 to SM-C, and award 0726113 to SLM), and the Department of Medical Physics and Bioengineering and the Mercer’s Institute for Research on Ageing in St. James’s Hospital Dublin (to DC) JO-M was a Fellow of the Pedro Barrié de la Maza Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Neuroscience

                fixational eye movements,tremor,fading,neural adaptation,saccadic adaptation

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