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The optical tweezers set-up (Fig. 1) is based on an inverted microscope (Axiovert S 100 TV, Carl Zeiss, Jena, Germany) which is designed for epi-illumination fluorescence microscopy.
To demonstrate our approach we lit several scenes, mainly using a direct illumination renderer designed for computer cinematography, but also including examples of global illumination and non-photorealistic rendering styles.
The initial plan was to use commercially available hand-held LED illumination systems designed for GFP detection.
The new Lumen 1600-LED fluorescence illumination system is designed for the most advanced fluorescent techniques; however, it has intuitive controls making it easy to use.
We propose herein to use a DCFC previously designed for endoscopy and taper down its illumination branch until the optimal ratio d/MFD is obtained (see Fig. 2(a)).
Since the PL is designed for focusing 632.8-nm 632.8-nm beams, under thincidentination the focus spot is located at the center of the PL.
The "instant structured illumination microscope" (iSIM) is a system designed for this purpose.
A controlled atmosphere setup designed for long-term degradation studies of organic solar cells under illumination is presented.
The diffusers were designed for the purpose of this study and ensured a uniform illumination over the entire visual field.
Skin erythema was evaluated by visual observation under constant tungsten illumination, and under conditions where room lighting was designed for red color rendering.
At low monochromatic homogeneous illumination (Glow = 1.8 W/cm2, λ0 = 809 nm) conversion efficiency of the cell, designed for a low irradiance, is reduced by 3.7%abs.
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