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      The brain creates illusions not just for us: sharks ( Chiloscyllium griseum) can “see the magic” as well

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          Abstract

          Bamboo sharks ( Chiloscyllium griseum) were tested for their ability to perceive subjective and illusionary contours as well as line length illusions. Individuals were first trained to differentiate between squares, triangles, and rhomboids in a series of two alternative forced-choice experiments. Transfer tests then elucidated whether Kanizsa squares and triangles, grating gaps and phase shifted abutting gratings were also perceived and distinguished. The visual systems of most vertebrates and even invertebrates perceive illusionary contours despite the absence of physical luminance, color or textural differences. Sharks are no exception to the rule; all tasks were successfully mastered within 3–24 training sessions, with sharks discriminating between various sets of Kanizsa figures and alternative stimuli, as well as between subjective contours in >75% of all tests. However, in contrast to Kanizsa figures and subjective contours, sharks were not deceived by Müller-Lyer (ML) illusions. Here, two center lines of equal length are comparatively set between two arrowheads or –tails, in which case the line featuring the two arrow tails appears to be longer to most humans, primates and birds. In preparation for this experiment, lines of varying length, and lines of unequal length randomly featuring either two arrowheads or -tails on their ends, were presented first. Both sets of lines were successfully distinguished by most sharks. However, during presentation of the ML illusions sharks failed to succeed and succumbed either to side preferences or chose according to chance.

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          Most cited references54

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          Teleostean and mammalian forebrains contrasted: Evidence from genes to behavior.

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            A theory of visual interpolation in object perception.

            We describe a new theory explaining the perception of partly occluded objects and illusory figures, from both static and kinematic information, in a unified framework. Three ideas guide our approach. First, perception of partly occluded objects, perception of illusory figures, and some other object perception phenomena derive from a single boundary interpolation process. These phenomena differ only in respects that are not part of the unit formation process, such as the depth placement of units formed. Second, unit formation from static and kinematic information can be treated in the same general framework. Third, spatial and spatiotemporal discontinuities in the boundaries of optically projected areas are fundamental to the unit formation process. Consistent with these ideas, we develop a detailed theory of unit formation that accounts for most cases of boundary perception in the absence of local physical specification. According to this theory, discontinuities in the first derivative of projected edges are initiating conditions for unit formation. A formal notion of relatability is defined, specifying which physically given edges leading into discontinuities can be connected to others by interpolated edges. Intuitively, relatability requires that two edges be connectable by a smooth, monotonic curve. The roots of the discontinuity and relatability notions in ecological constraints on object perception are discussed. Finally, we elaborate our approach by discussing related issues, some new phenomena, connections to other approaches, and issues for future research.
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              Evolution of the telencephalon in nonmammals.

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                Author and article information

                Journal
                Front Neural Circuits
                Front Neural Circuits
                Front. Neural Circuits
                Frontiers in Neural Circuits
                Frontiers Media S.A.
                1662-5110
                20 March 2014
                2014
                : 8
                : 24
                Affiliations
                Department for Comparative Sensory Biology and Neurobiology, Institute of Zoology, Rheinische Friedrich-Wilhelms-University Bonn Bonn, Germany
                Author notes

                Edited by: Davide Zoccolan, International School for Advanced Studies, Italy

                Reviewed by: Andreas Nieder, University of Tübingen, Germany; Guy Wallis, University of Queensland, Australia

                *Correspondence: Theodora Fuss, Department for Comparative Sensory Biology and Neurobiology, Institute of Zoology, Rheinische Friedrich-Wilhelms-University Bonn, Poppelsdorfer Schloss, Meckenheimer Allee 169, 53115 Bonn, Germany e-mail: thfuss@ 123456uni-bonn.de

                This article was submitted to the journal Frontiers in Neural Circuits.

                Article
                10.3389/fncir.2014.00024
                3960505
                24688458
                938355ca-f63c-49d7-9ae2-44a84e4cee20
                Copyright © 2014 Fuss, Bleckmann and Schluessel.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 27 January 2013
                : 03 March 2014
                Page count
                Figures: 11, Tables: 4, Equations: 0, References: 73, Pages: 17, Words: 12363
                Categories
                Neuroscience
                Original Research Article

                Neurosciences
                optical illusion,kanizsa,subjective contour,müller-lyer deception,elasmobranch,chiloscyllium griseum

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