A New Method of Translational Compensation for Spatial Precession Targets with Rotational Symmetry

Author(s):  
Rong CHEN ◽  
Cunqian FENG ◽  
Sisan HE ◽  
Yi RAO
PLoS ONE ◽  
2021 ◽  
Vol 16 (7) ◽  
pp. e0254361
Author(s):  
Alexis D. J. Makin ◽  
John Tyson-Carr ◽  
Yiovanna Derpsch ◽  
Giulia Rampone ◽  
Marco Bertamini

An Event Related Potential (ERP) component called the Sustained Posterior Negativity (SPN) is generated by regular visual patterns (e.g. vertical reflectional symmetry, horizontal reflectional symmetry or rotational symmetry). Behavioural studies suggest symmetry becomes increasingly salient when the exemplars update rapidly. In line with this, Experiment 1 (N = 48) found that SPN amplitude increased when three different reflectional symmetry patterns were presented sequentially. We call this effect ‘SPN priming’. We then exploited SPN priming to investigate independence of different symmetry representations. SPN priming did not survive changes in retinal location (Experiment 2, N = 48) or non-orthogonal changes in axis orientation (Experiment 3, N = 48). However, SPN priming transferred between vertical and horizontal axis orientations (Experiment 4, N = 48) and between reflectional and rotational symmetry (Experiment 5, N = 48). SPN priming is interesting in itself, and a useful new method for identifying functional boundaries of the symmetry response. We conclude that visual regularities at different retinal locations are coded independently. However, there is some overlap between different regularities presented at the same retinal location.


Author(s):  
C. C. Clawson ◽  
L. W. Anderson ◽  
R. A. Good

Investigations which require electron microscope examination of a few specific areas of non-homogeneous tissues make random sampling of small blocks an inefficient and unrewarding procedure. Therefore, several investigators have devised methods which allow obtaining sample blocks for electron microscopy from region of tissue previously identified by light microscopy of present here techniques which make possible: 1) sampling tissue for electron microscopy from selected areas previously identified by light microscopy of relatively large pieces of tissue; 2) dehydration and embedding large numbers of individually identified blocks while keeping each one separate; 3) a new method of maintaining specific orientation of blocks during embedding; 4) special light microscopic staining or fluorescent procedures and electron microscopy on immediately adjacent small areas of tissue.


Author(s):  
L. Reimer ◽  
R. Oelgeklaus

Quantitative electron energy-loss spectroscopy (EELS) needs a correction for the limited collection aperture α and a deconvolution of recorded spectra for eliminating the influence of multiple inelastic scattering. Reversely, it is of interest to calculate the influence of multiple scattering on EELS. The distribution f(w,θ,z) of scattered electrons as a function of energy loss w, scattering angle θ and reduced specimen thickness z=t/Λ (Λ=total mean-free-path) can either be recorded by angular-resolved EELS or calculated by a convolution of a normalized single-scattering function ϕ(w,θ). For rotational symmetry in angle (amorphous or polycrystalline specimens) this can be realised by the following sequence of operations :(1)where the two-dimensional distribution in angle is reduced to a one-dimensional function by a projection P, T is a two-dimensional Fourier transform in angle θ and energy loss w and the exponent -1 indicates a deprojection and inverse Fourier transform, respectively.


1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  

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