However, the top-down ensemble mean produces an emission shift between 2006 and 2008, leading to 22 [16 32] Tg CH4 yr−1 higher methane emissions over the period 2008 2012 compared to 2002 2006.
The example shown is a search for all monomeric, constitutively fluorescent (non-photochromic) proteins that have an emission maximum between 500 and 560 and a molecular brightness that is at least 1.5-fold higher than the average brightness of all similarly colored (excitation maximum within 30 nm) proteins in the database published since 2010.
Recently, ZnO NTs/Au Schottky LED has been reported covering an emission spectrum between 400 and 600 nm [12].
The FRET effect was further shown by an emission comparison between conjugated AlPcSs and free AlPcSs under the excitation at 532 nm (Figure 2c).
Using these findings, an emission maximum between 750 and 800 nm is likely to have a reflectance transition edge between approximately 500 and 550 nm, suggesting a yellow Cd/S/Se pigment was possibly used.
Cells at 95% confluence were UV-irradiated by using a TL20W/12RS UV lamps (Philips, Eindhoven, Netherlands) with an emission spectrum between 275 and 380 nm (peak, 310 315 nm) [38].
Subsequently, they were excited at 490 nm and subjected to an emission scan between 500 and 620 nm in a JASCO FP-6300 spectrofluorometer.
Whole cells were also positively monitored by fluorescence emission on an advanced bio-spectrum imaging system using an emission filter between 500 to 523 nm (UVP, LLC, Upland, CA).
The sample excitation was carried out with an Argon Laser at 488 nm (λexe 488) with a λ step size of 3 nm for an emission wavelength between 550 and 748 nm.
Plants were exposed 5 hours to low temperature (4°C) and high PPFD (1.200 μmol photons m-2 s-1) provided by two 450 watts metal-halide lamps (HQI-TS, Osram, Berlin, Germany) with a emission peak between 500 and 600 nm.
