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Wind speed was also measured and collected every 5 min using an anemometer.
Each solution was then ultrasonicated for 20 min using an ultrasonication probe until a homogeneous suspension was achieved.
The samples were homogenized for about 5 min using an ultrasonic disrupter to ensure proper dispersion of the nanoparticles.
The collected soil was sterilized at 1.05 121 °C (121 °C) for 15 min using an autoclave.
In the fabrication process, the stainless steel wafer prepared in the first step was cleaned with acetone for 20 min using an ultrasonic washing machine.
The bacterial suspensions were then centrifuged at 4,000 rpm for 5 min using an Eppendorf MiniSpin centrifuge (Eppendorf, Hamburg, Germany) to pelletize the cells.
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Also, a DRE of SF6 was 99.99% at the N2 flow rate of 60 L/min using an applied microwave power of 6 kW.
Melting points were measured at a rate of 5 °C/min using an X-5 micro melting point apparatus (Beijing, China) and were not corrected.
Adaxial reflectance spectra of leaves were recorded at a rate of 600 nm/min using an U-3010 spectropHitachier (HiTokyo, Japan, Japan) equipped with an integrating sphere attachment.
Video recordings of microscopic fields were made continuously (1 image/min) using an in house developed software program version of the IPlab 3.5.5.
The scanning rate is 2°/min using an automatic divergence slit assembly and a proportional detector.
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