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The performance of the analysis (convergence of the independent runs, effective sample sizes) was evaluated using Tracer v.1.4.1 [ 22].
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For example, soot primary particle sizes were evaluated using combined LII and ELS, showing decreasing particle sizes for increasing concentrations of potassium, in reasonable agreement with particle sizes evaluated using transmission electron microscopy.
Total pore volume and sizes were evaluated using the standard Barrett Joyner Halenda (BJH) treatment.
Different time window sizes were evaluated using mean of features and mean of scores with LBP-TOP 8, 8, 8, 1, 1, 1 u 2. (a) Replay-Attack Database (HTER %).
Fragment sizes were evaluated using GeneMapper v3.7 software (Applied Biosystems), and the molecular data-points for all SSR markers are listed in Table S4.
Effect sizes were evaluated using Cohen's d statistics [ 48].
Effect sizes were evaluated using the partial eta-squared statistic.
The RNA concentrations were determined by the NanoDrop, and the transcript sizes were evaluated using a Bioanalyser.
The aerodynamic particle size was evaluated using a next generation impactor (model 170 NGI, MSP Corporation), which was equipped with a pre-separator [12].
Fragment size was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technologies, CA, USA), and the purities of the fragments were determined using a Bioanalyzer HS DNA Kit, a Qubit dsDNA HS Assay Kit (Invitrogen), and a Qubit 2.0 Fluorometer (Invitrogen).
The effect of Ubx depletion on leg segment size was evaluated using one-tail T-test.
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