The ZnO suspensions with methyl orange were illuminated continuously with light from a 30 W mercury lamp (2,537 Å).
Samples were illuminated continuously with a 488-nm laser for 10 min, and fluorescent images were taken at 0, 1, 5, and 10 min.
These effects were observed regardless of whether the electrodes were illuminated continuously or illuminated only before the polarization scans, and appear to be independent of the wavelength of the incident light in the wavelength region 300 to 450 nm.
The cultures were illuminated continuously with warm white fluorescent lamps providing the irradiance of 40 42 μmol m−2 s−1 photosynthetic photon flux density and stirred by shaking two times a day.
The sample was illuminated continuously with 570-nm laser and the integration time was 30 ms for each frame.
During the imaging protocol we illuminated continuously for a 1 min period to observe the extent of fluorescence decrease, and resumed imaging at 1 min intervals to quantify the extent of reversible photoswitching (Figure 3A, B).
Context B consisted of plastic flooring covered with fresh bedding, altered geometry and spatial cues (red and black tape) relative to context A, four additional cue lights illuminated continuously, and 1% ammonium hydroxide solution used as a cleaning agent.
The culture was illuminated continuously at a light intensity of approximately 250 μmol m−2 s−1.
The culture was illuminated continuously with a light intensity of approximately 150 μmol m-2 s-1.
To generate cultures for H2 measurement and RNA harvesting, C. moewusii SAG 24.91 cultures were grown in 1-L Roux bottles using TAP media at 25°C, and illuminated continuously with white fluorescent light (200 μmol photons m-2 s-1).
The vessels were illuminated with continuously fluorescence light at a photon flux density of 100 μmol m−2 s−1.
