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The size of the analysed zones depended on the microscopy magnification.
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In order to fully understand the similarities and differences, the same detailed investigation for each spectral region was performed (see also supplementary figures A-C and relevant captions) and the curve fitting results hereafter discussed, subdivided for each analysed zone, as reported in Table 2.
The UN's World Food Programme (WFP) says: "In June, the famine early-warning systems network said it had compared rainfall data for Kenya and Ethiopia and concluded that 2010-11 was the driest or second driest year since 1950-51 in 11 of 15 analysed pastoral zones.
Figure S10, Mean azimuth of the normal lines to the trench for the analysed subduction zones.
Table S1, Mean azimuth of the normal lines to the trench for the analysed subduction zones.
Before contamination, soil gas samples were extracted from SP3 SP7 (vadose zone) and SP8 (groundwater zone) and analysed for background concentrations of gasoline compounds.
Water masses, Fronts, Inter-Frontal and Frontal Zones are analysed and classified: (a) the water masses: Tropical Low-Salinity Water, Tropical Surface Water, Tropical Tropospheric Water, Subtropical Low-Salinity, Subtropical Surface Water, Subtropical Tropospheric Water Water, Tropical Tropospheric Water, Subtropical Low-Salinity, Subtropical Surface Water, Subtropical Tropospheric Water
These zones were analysed quantitatively using the imaging system specified above.
In addition to this, the time spent and distance covered in the following five relative speed zones were analysed, which were derived using the peak speed (V max) obtained by both devices [ 20]: <20% V max very low," 20 50% V max low," 51 80% V max moderate," 81 95% V max—"high," >95% V max very high".
This reduction in sample size for subgroup analyses will result in fewer women/births being available but the same number of areas (data zones) will be analysed (apart from analyses restricted to those living in the most deprived areas).
Isolates that did not show an inhibition zone were analysed via colony PCR with three primer sets: amdS, for the selection marker (primers 13 and 14); penDE, as indicator for the presence or absence of the penicillin biosynthetic gene cluster (primers 15 and 16) and niaA as an internal control (primers 17 and 18; Table 1).
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