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Microsamples taken from representative areas of the object were analysed (Table 1).
It was therefore proposed that in this situation that a conservator would swab selected areas of the object surface.
Thicker areas of the object or areas with higher refractive indices will yield larger OT values as shown in the profile on the bottom of Fig. 3.
Motion can cause some areas of the object to be sampled multiple times during acquisition, while other areas may be unsampled as shown in Fig. 3.
Further, by normalisation of the signal wavelength, we determine the optical path difference of the two waves or phase height (thickness) of the object at a given point and create the phase portrait of a cell that represents the distribution of the phase shift in various areas of the object.
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Laser-induced luminescence spectra from different areas of the objects and traditional digital imaging, using led-based lamps, long pass filters and a commercial photographic camera, complement the results from photoluminescence lifetime imaging.
(b) Area of the object after digitization.
Figure 4 shows a histogram of an area of the object in two frames of image.
This sample corresponds to an area of the object where macroscopical delamination (separation of layers) is visible.
After the cameras were calibrated, photos were taken of each object from an evenly distributed quantity of positions and angles around the surrounding area of the object.
The spot area of the object expected from the X-ray luminosity is more than 1 order of magnitude larger than that estimated from the amplitude of quasi-periodic modulations.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com