2020 ◽  
Vol 3 (5) ◽  
pp. 494-503
Author(s):  
Xi Li ◽  
Zhixiang Wang ◽  
Xiaohua Wang ◽  
Mingzhe Rong ◽  
Di Liu

2021 ◽  
Author(s):  
Drago A. Guggiana Nilo ◽  
Clemens Riegler ◽  
Mark Hübener ◽  
Florian Engert

2011 ◽  
Vol 11 (8) ◽  
pp. 8-8 ◽  
Author(s):  
D. V. D'Souza ◽  
T. Auer ◽  
H. Strasburger ◽  
J. Frahm ◽  
B. B. Lee

2010 ◽  
Vol 24-25 ◽  
pp. 123-128 ◽  
Author(s):  
Claudia Garza ◽  
Anthony G. Deakin ◽  
G.R. Jones ◽  
J.W. Spencer ◽  
K.K.B. Hon

The present contribution describes a chromatic processing approach for quantifying the two dimensional, polychromatic interference patterns produced by a strained photo-elastic element and recorded with a CCD camera. The outputs from the three R, G, B channels of the camera covering a selected area of the interference pattern are processed to yield three chromatic parameters which are H (dominant signal wavelength), L (nominal signal strength), S (effective wavelength spread of signal). It is shown that the value of each of the three parameters varies with strain in a quasi cyclical manner, all being out of phase with each other. Consequently the strain measurement range and sensitivity can both be optimized by the use of the appropriate chromatic parameter within different strain ranges.


2019 ◽  
Vol 36 ◽  
Author(s):  
Ralph F. Nelson ◽  
Annika Balraj ◽  
Tara Suresh ◽  
Meaghan Torvund ◽  
Sara S. Patterson

Abstract There are four cone morphologies in zebrafish, corresponding to UV (U), blue (B), green (G), and red (R)-sensing types; yet genetically, eight cone opsins are expressed. How eight opsins are physiologically siloed in four cone types is not well understood, and in larvae, cone physiological spectral peaks are unstudied. We use a spectral model to infer cone wavelength peaks, semisaturation irradiances, and saturation amplitudes from electroretinogram (ERG) datasets composed of multi-wavelength, multi-irradiance, aspartate-isolated, cone-PIII signals, as compiled from many 5- to 12-day larvae and 8- to 18-month-old adult eyes isolated from wild-type (WT) or roy orbison (roy) strains. Analysis suggests (in nm) a seven-cone, U-360/B1-427/B2-440/G1-460/G3-476/R1-575/R2-556, spectral physiology in WT larvae but a six-cone, U-349/B1-414/G3-483/G4-495/R1-572/R2-556, structure in WT adults. In roy larvae, there is a five-cone structure: U-373/B2-440/G1-460/R1-575/R2-556; in roy adults, there is a four-cone structure, B1-410/G3-482/R1-571/R2-556. Existence of multiple B, G, and R types is inferred from shifts in peaks with red or blue backgrounds. Cones were either high or low semisaturation types. The more sensitive, low semisaturation types included U, B1, and G1 cones [3.0–3.6 log(quanta·μm−2·s−1)]. The less sensitive, high semisaturation types were B2, G3, G4, R1, and R2 types [4.3-4.7 log(quanta·μm−2·s−1)]. In both WT and roy, U- and B- cone saturation amplitudes were greater in larvae than in adults, while G-cone saturation levels were greater in adults. R-cone saturation amplitudes were the largest (50–60% of maximal dataset amplitudes) and constant throughout development. WT and roy larvae differed in cone signal levels, with lesser UV- and greater G-cone amplitudes occurring in roy, indicating strain variation in physiological development of cone signals. These physiological measures of cone types suggest chromatic processing in zebrafish involves at least four to seven spectral signal processing pools.


1990 ◽  
Vol 5 (6) ◽  
pp. 547-555 ◽  
Author(s):  
D. I. Flitcroft

AbstractAccommodation is more accurate with polychromatic stimuli than with narrowband or monochromatic stimuli. The aim of this paper is to develop a computational model for how the visual system uses the extra information in polychromatic stimuli to increase the accuracy of accommodation responses. The proposed model is developed within the context of both trichromacy and also the organization of spatial and chromatic processing within the visual cortex.The refractive error present in the retinal image can be estimated by comparing image quality with and without small additional changes in refractive state. In polychromatic light, the chromatic aberration of the eye results in differences in ocular refractive power for light of different wavelengths. As a result, the refractive state of the eye can be estimated by comparing image quality in the three types of cone photoreceptor. The ability of cortical neurons to perform such comparisons on image quality with a crude form of spatial-frequency analysis is examined theoretically. It is found that spatially band-pass chromatically opponent neurons (that may correspond to double opponent neurons) can perform such calculations and that chromatic cues to accommodation are extracted most effectively by neurons responding to spatial frequencies of between 2 and 8 cycles/deg.


2012 ◽  
Vol 24 (4) ◽  
pp. 819-829 ◽  
Author(s):  
Henry Railo ◽  
Niina Salminen-Vaparanta ◽  
Linda Henriksson ◽  
Antti Revonsuo ◽  
Mika Koivisto

Chromatic information is processed by the visual system both at an unconscious level and at a level that results in conscious perception of color. It remains unclear whether both conscious and unconscious processing of chromatic information depend on activity in the early visual cortex or whether unconscious chromatic processing can also rely on other neural mechanisms. In this study, the contribution of early visual cortex activity to conscious and unconscious chromatic processing was studied using single-pulse TMS in three time windows 40–100 msec after stimulus onset in three conditions: conscious color recognition, forced-choice discrimination of consciously invisible color, and unconscious color priming. We found that conscious perception and both measures of unconscious processing of chromatic information depended on activity in early visual cortex 70–100 msec after stimulus presentation. Unconscious forced-choice discrimination was above chance only when participants reported perceiving some stimulus features (but not color).


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