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SOC of each fraction was analysed with a LECO Truspec CN analyser following the ISO 10694:1195, and expressed on a sand-free basis20.
The percentage of cells at distinct phases of the cell cycle was analysed with a Beckman Coulter – CyAn2 ADP analyser (Beckman Coulter, UK).
A Salmonella outbreak was analysed with a case case study design in order to test the applicability of this method.
Plagioclase was analysed with a focused beam or area analyses (~5 × 5 μm2) and matrix glasses were analysed with area analyses (10 × 10 to 30 × 30 μm2).
The interaction of the peptides with MN12H2 was analysed with a surface plasmon resonance competition assay yielding equilibrium binding constants in solution (KS).
For each sample, the proportion of stones (>2 mm), coarse sand (250 2000 μm) and fine sand (53 250 μm) was analysed with a modification of the ISO 11277: 1998 for particle size analysis.
Each of the three behavioural states was analysed with a separate GLMM, with the response variable being 0 or 1 for each GPS location with treatment, coded as a three-level factor, as a predictor.
The concentration of purified DNA was determined using the Qubit 3.0 Fluorometer (Thermo Fisher Scientific) and DNA size was analysed with a Bioanalyzer High sensitivity DNA chip (Agilent Technologies).
The observed fuel cell behaviour was analysed with a mathematical model which consists of anode mass balances, charge balances of both electrodes and electrode kinetic expressions.
The model structure was analysed with a novel numerical topology algorithm for calculating the concentration of tie chains and trapped entanglements.
Each image was analysed with a dedicated MatLab program for extrapolation of the fluorescence intensity.
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