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Checkerboard Pattern (checkerboard + pattern)
Selected AbstractsNeuroanatomical correlates of the near response: voluntary modulation of accommodation/vergence in the human visual systemEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 1 2000Hans O. Richter Abstract This study identifies brain regions participating in the execution of eye movements for voluntary positive accommodation (VPA) during open-loop vergence conditions. Neuronal activity was estimated by measurement of changes in regional cerebral blood flow (rCBF) with positron emission tomography and 15O-water. Thirteen naive volunteers viewed a checkerboard pattern with their dominant right eye, while a lens interrupted the line of gaze during alternate 1.5 s intervals. Three counterbalanced tasks required central fixation and viewing of a stationary checkerboard pattern: (i) through a 0.0 diopter (D) lens; (ii) through a ,5.0-D lens while avoiding volitional accommodation and permitting blur; and (iii) through a ,5.0-D lens while maintaining maximal focus. The latter required large-amplitude, high-frequency VPA. As an additional control, seven of the subjects viewed passively a digitally blurred checkerboard through a 0.0-D lens as above. Optometric measurements confirmed normal visual acuity and ability to perform the focusing task (VPA). Large-amplitude saccadic eye movements, verified absent by electro-oculography, were inhibited by central fixation. Image averaging across subjects demonstrated multifocal changes in rCBF during VPA: striate and extrastriate visual cortices; superior temporal cortices; and cerebellar cortex and vermis. Decreases in rCBF occurred in the lateral intraparietal area, prefrontal and frontal and/or supplementary eye fields. Analysis of regions of interest in the visual cortex showed systematic and appropriate task dependence of rCBF. Activations may reflect sensorimotor processing along the reflex arc of the accommodation system, while deactivations may indicate inhibition of systems participating in visual search. [source] Tetrakis(,2 -4-aminobenzoato)di-,3 -oxido-tetrakis[dibutyltin(IV)]ACTA CRYSTALLOGRAPHICA SECTION C, Issue 3 2010Anthony Linden The molecule of the title compound, [Sn4(C4H9)8(C7H6NO2)4O2], lies about an inversion centre and is a tetranuclear bis(tetrabutyldicarboxylatodistannoxane) complex containing a planar Sn4O2 core in which two ,3 -oxide O atoms connect an Sn2O2 ring to two exocyclic Sn atoms. Each Sn atom has a highly distorted octahedral coordination. In the molecule, the carboxylate groups of two aminobenzoate ligands bridge the central and exocyclic Sn atoms, while two further aminobenzoate ligands have highly asymmetric bidentate chelation to the exocyclic Sn atoms plus long O...Sn interactions with the central Sn atoms. Each Sn atom is also coordinated by two pendant n -butyl ligands, which extend roughly perpendicular to the plane of the Sn4O10 core. Only one of the four unique hydrogen-bond donor sites is involved in a classic N,H...O hydrogen bond, and the resulting supramolecular hydrogen-bonded structure is an extended two-dimensional network which lies parallel to the (100) plane and consists of a checkerboard pattern of four-connected molecular cores acting as nodes. The amine groups not involved in the hydrogen-bonding interactions have significant N,H..., interactions with neighbouring aminobenzene rings. [source] Hypothesis testing in distributed source models for EEG and MEG dataHUMAN BRAIN MAPPING, Issue 2 2006Lourens J. Waldorp Abstract Hypothesis testing in distributed source models for the electro- or magnetoencephalogram is generally performed for each voxel separately. Derived from the analysis of functional magnetic resonance imaging data, such a statistical parametric map (SPM) ignores the spatial smoothing in hypothesis testing with distributed source models. For example, when intending to test a single voxel, actually an entire region of voxels is tested simultaneously. Because there are more parameters than observations, typically constraints are employed to arrive at a solution which spatially smooths the solution. If ignored, it can be concluded from the hypothesis test that there is activity at some location where there is none. In addition, an SPM on distributed source models gives the illusion of very high resolution. As an alternative, a multivariate approach is suggested in which a region of interest is tested that is spatially smooth. In simulations with MEG and EEG it is shown that clear hypothesis testing in distributed source models is possible, provided that there is high correspondence between what is intended to be tested and what is actually tested. The approach is also illustrated by an application to data from an experiment measuring visual evoked fields when presenting checkerboard patterns. Hum Brain Mapp, 2005. © 2005 Wiley-Liss, Inc. [source] Polygonal finite elements for topology optimization: A unifying paradigmINTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN ENGINEERING, Issue 6 2010Cameron Talischi Abstract In topology optimization literature, the parameterization of design is commonly carried out on uniform grids consisting of Lagrangian-type finite elements (e.g. linear quads). These formulations, however, suffer from numerical anomalies such as checkerboard patterns and one-node connections, which has prompted extensive research on these topics. A problem less often noted is that the constrained geometry of these discretizations can cause bias in the orientation of members, leading to mesh-dependent sub-optimal designs. Thus, to address the geometric features of the spatial discretization, we examine the use of unstructured meshes in reducing the influence of mesh geometry on topology optimization solutions. More specifically, we consider polygonal meshes constructed from Voronoi tessellations, which in addition to possessing higher degree of geometric isotropy, allow for greater flexibility in discretizing complex domains without suffering from numerical instabilities. Copyright © 2009 John Wiley & Sons, Ltd. [source] Backward masking and visual mismatch negativity: Electrophysiological evidence for memory-based detection of deviant stimuliPSYCHOPHYSIOLOGY, Issue 4 2007István Czigler Abstract Sequences composed of two different colored checkerboard patterns (standard and deviant) were presented to adults. Each pattern was followed by a mask with stimulus onset asynchronies (SOAs) varying between 14 and 174 ms. ERPs were recorded to the deviant and standard stimuli while the participants detected changes of a cross, which was continuously present at the center of the screen. In further experiments, the participants performed a Go-NoGo task detecting the deviant checkerboards. Deviant stimuli elicited an occipital negative component with 124,132 ms mean latency (the visual mismatch negativity, vMMN) at test (standard or deviant)-to-mask SOAs longer than 27 ms. No vMMN amplitude increase was observed beyond 40 ms test-to-mask intervals, whereas detection of deviant checkerboard patterns improved up to 174-ms SOA. Therefore the processes underlying vMMN elicitation cannot fully explain the overt detection of visual deviance. [source] |