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The intensities were calibrated to the lamp spectra baseline.
The detected UV lamp spectra of the XL-A and MWL detectors agree quite well so that a similar performance can be expected in the UV range.
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Spectral data was divided by the normalized lamp spectrum to calibrate for variations in lamp intensity.
NIR spectrometers were calibrated with Ne lamp spectrum before and after measurements.
The spectral data was calibrated for variations in lamp intensity by dividing by the normalized lamp spectrum.
When illuminating with the whole lamp spectrum, the variation in the photocurrent intensity from very low ambient light to the maximum impinging light intensity showed an increase of more than three orders of magnitude, fully reproducible for the same gold plot.
We determined incident irradiance using a calibrated radiometer (IL1700, SED 240/W; International Light, Peabody, MA) and calculated delivered UVC fluence with a spreadsheet program that included lamp spectrum, solution absorbance, exposure time, and incident irradiance (Bolton and Linden 2003).
The results showed that the lack of the visible part of the incandescent lamp light spectrum (17% of the lamp light intensity) reduced hydrogen production by 50%.
The absorption spectrum of macular pigment was calculated by subtracting the measured normalized reflectance spectrum from the normalized lamp's illumination spectrum in the range 475 nm–520 nm and averaging over pixels in the circled area.
The excitation source was a 450 W Xe arc lamp and all spectra were corrected for detection and optical spectral response (instrumental functions) of the spectrofluorimeter.
In order to acquire the absorption spectrum in the same area, the lamp's illumination spectrum S i was first measured by placing a white paper in front of the retinal camera's front lens and averaging over pixels' reflectance spectra in the field of view.
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