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UV illumination (b).
Visible illumination (b).
These are, as described by Beauchemin and Barron [1], (a) uniform illumination, (b) surfaces with Lambertian reflectance, and (c) movement limited to the plane of the image.
Fig. 4 Subcellular localization of the HOG1 GFP fusion protein in response to changes in osmotic pressure (a), and after illumination (b) of the cells with blue light.
Figure 7 EIS spectra (Nyquist plots) of protein coated hematite recorded in dark a) and under illumination b) for DC bias from 0 mV to 1000 mV.
Figure 6 EIS spectra (Nyquist plots) of pristine hematite in dark a) and under illumination b) for DC bias from 0 mV to 1000 mV.
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The selection of these areas was focussed on four types of evidence: (a) the planning process in both text copying and painted illuminations; (b) the relationship between pigments used in the illuminations and texts; (c) the relationship between coloured texts and the texts written in ink; and (d) the pigment and binder identification and their manner of use.
Fig. 3 J-V characteristics of the DSSCs fabricated with the Pt, PPy, and PPy@Pt CEs under the standard illumination (a, b).
Fig. 7 Current density-voltage (J-V) characteristics of 0.4-μm SiNW cells with and without surface treatment under a illumination and b dark condition.
The reaction under visible light illumination (line: b in Fig. 4a) shows increased reduction of toluene vapour with time, representing photocatalytic degradation in addition to leakages and adsorptions.
Fig. 2 a Illumination geometry, b photography of the mechanical head with a sample on test, white spot results of the mixing of the three R-G-B laser lines.
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