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The stimulated emission cross-section for the 1064 nm emission was determined using the emission spectra.
CH4 emission was determined by the closed chamber method at 10-day interval during rice growing period in a loamy clay paddy soil.
The excitation wavelength at 272 nm and the λmax of emission was determined by scanning the standard solution 250 500 nm.
Corrected intensity functions of light absorption with sample, I ex(λ sam), were also determined from excitation spectra of the system (450 480 nm, scan rate 60 nm/min), whereas the corrected intensity function of the emission was determined from emission spectra (I em, 550 800 nm, scan rate 60 nm/min).Quantum yield was calculated from the equation as follows [45, 46]: (2).
Normalized light emission was determined by dividing the FLuc reading by the GLuc reading and normalized TF activity was determined by dividing the normalized light emission for each sample by the average normalized light emission for TA.
The fluorescence of ANS emission was determined at 516 nm in the presence of CIP and CMP and in the absence of antibiotic.
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Carbon losses in soil sediment, dissolved organic carbon (DOC) and CO2 emission were determined.
These coatings were investigated, and their viscosity, wettability, and gas volume emission were determined.
The optimal number of devices, the Levelized Cost of Energy (LCE) and the CO2 emission were determined for each solution.
The cycle threshold (Ct) values, corresponding to the PCR cycle number at which fluorescence emission reaches a threshold above baseline emission, were determined and the mRNA and miRNA levels calculated using the comparative 2-ΔΔCt method.
In fact, TPL emission is determined by instantaneous incident power.
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emission was centered
emission was used
emission was carried
emission was synthesized
emission was related
emission was suppressed
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