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N=750 samples were set for each frequency band.
The dependent variables of healthy samples were set as 0, and diseased samples were set as 1, 2, 3, 4 and 5 according to infection severities, respectively.
The samples were set up by mixing soil samples with various content of stabilizer at optimum water content.
In this process, the AISI 316L austenitic stainless steel samples were set on a plate at anodic potential.
The values of the controls (wells with cells and no samples) were set to 100% cell viability.
The standard samples were set up and extracted in the same way as the leachate water samples.
In the laboratory, the diatom samples were set aside for 2 days to sediment before being processed using potassium permanganate method according to Taylor et al. (2005).
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Ru (proportion of negative samples) was set to 1/16 of negative samples.
Different cuts are collected at different top tray temperatures and samples are set aside for analysis.
The distance between the evaporation boat and the samples was set to 35 cm.
The number of support samples is set as 5 in this experiment.
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