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A large scale plot (50 × 50 m2) with 8 Q7.1 s and 16 soil heat flux plates was firstly designed to quantify the spatial variability in Rn and G approximately to match with the source area with H and LE.
We designed a large scale plot (50 × 50 m2) with 8 Q7.1 s and 16 soil heat flux plates to quantify the spatial variability in Rn and G approximately to match with the source area with H and LE.
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It will operate in a scanning mode from a sun-synchronous orbit, using low temperature detectors (at 0.1 K) and located inside a telescope that is cooled to approximately 2.73 K – to match the background temperature.
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Randomization was balanced to match approximately for age (≥15 years versus <15 years) and sex.
Ethnically matched controls were sampled from these centres to match approximately the geographical distribution of the cases.
Simulation parameters (N = 1000 trajectories, A = 10 μm, ℓ = 60 μm, V = 50 μm/s) were chosen to match approximately those for viscosity 1 mPa·s in Figure 2C.
From this dataset we also generated degraded growth cone outlines to match approximately the quality of outlines available using the plastic substrate.
A volume of 100 μL of the above standardized inocula was then added into each well to match approximately 2.5×10 CFU.mL−1 for yeast and 10 CformL−1 for dermatophytes in a total volume of 200 μL.
The price of HSA would have to increase approximately five fold for TPE to match the cost of IVIg drug costs.
Primer pairs for five MLV target regions were designed such that each primer pair generated PCR products of approximately 400 bp in length to match but not exceed the maximum read length of the GS FLX chemistry available at the time of sequence data generation.
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