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This variation is explained by the location of the cations in the spinel ferrite.
The reason for this variation is explained using temporal evolution of the measured velocity distribution of bubbles having different sizes.
This variation is explained in terms of efficiency of oxide growth, as well as of chemical composition, density, and porosity of the TiO2 nanotubular array.
This variation is explained by different methodologies.
This variation is explained by differences in the number of acrocentric and metacentric chromosomes among species.
This variation is explained in part by differences in the TAS content of different telomeres (Mondoux and Zakian 2007).
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This variation was explained by using, for the first time, molecular modelling and docking.
Selection patterns of individual cougars varied greatly, and some of this variation was explained by the functional response.
This variation was explained in terms of the electric percolation with a threshold at the volume fraction of 20 35%.
Multi-level, generalised linear mixed-effects modelling demonstrated that this variation was explained by: (i) the catch weight of school prawns; (ii) the particular estuary being fished; and (iii) random between-tow and -trawler variability.
This variation was explained by years since sowing of the alfalfa (standardized slope coefficient, β≈0.52), annual frequency of flood irrigation (β≈−0.43), habitat area as a percentage of the landscape within a 500 m buffer around the field (β≈0.31), season of the year (β≈0.25), field size (β≈−0.20) and percentage of sand within the top soil layer (β≈0.16).
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