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A calculated volume to area weighted particle size, D, (particle diameter or side length for non-spherical morphologies) was determined from specific surface area using the relationship [66]: where K s is the particle shape coefficient, ρ is particle density, and SBET is the specific surface area.
For quantification, the percentage of cells with abnormal mitochondrial morphologies was determined and taken as a measure of the proportion of cells with fragmented mitochondria.
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Particle morphologies were determined by Zeta Sizer, DLS, XRD and SAXS.
The cross-sectional and top-view morphologies are determined using a scanning electronic microscopy (SEM, JEOL-7500F).
The crystal morphologies are determined by a complex competition between the heat transport (far-field flux) and the strength of surface tension anisotropy.
Low-energy morphologies are determined by minimizing, with respect to shape parameters, the elastic microstrain energy associated with local incompatibility of transformation strains.
Identical terminal end buds (TEBs) were compared before and after fixation, staining, and whole mount preparation and structure of collagen networks and TEB morphologies were determined.
The species of individual colonies of different colors and morphologies were determined by using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
The formation of these different morphologies is determined by agglomeration of the nanocrystals, which have a similar size in all the investigated samples.
In the present study, the flagella of three tested bacteria and pili of E. coli were clearly observed in air, and their morphologies were determined accordingly by analyzing AFM height images.
Pollen morphology was determined by acetolysis (Shivanna and Rangaswamy 1993).
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