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The amount of time in which to learn the material is fixed, but the amount of learning varies significantly.
It is assumed that ϕ ≪ 1, and the thermal conductivity ratio of nanoparticle material and base fluid material is fixed and large.
In the chromosome spreading methodology, biological material is fixed, hydrolyzed, spread on a slide and stained using DNA-specific dyes, allowing for a visual chromosome or DNA quantification on a single cell basis [ 18].
The approach we propose here differs from other previous methods for visualizing floral cells because many of the preparation procedures that have been shown to have the largest impact on cell structure are avoided with this method; material is fixed before staining and imaging, thus samples do not need to be visualized immediately after collection.
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The diagnostic material was fixed in the routinely-used fixative.
Collected material was fixed in 96% ethanol and stored at −20/−80 °C until DNA extraction.
The total volume and the volume of high conductivity material are fixed, but their aspect ratio can vary.
The material was fixed at 2.5% glutaldehyde and 2% paraformaldehyde solution; post-fixed at 2% osmium tetroxide; dehydrated with increasing ethanol concentrations, and included in epoxy resin.
The element cross section and the wall material are fixed, while the shape of the fluid flow opening, or the wetted perimeter is free to vary.
We study the relative importance of uncertain facies geometry and uncertain hydraulic conductivity and porosity on predictions of catchment and solute time of travel to the pumping well by focusing on cases in which (1) the facies distribution is random, but the hydraulic properties of each material are fixed, and (2) both facies geometry and material properties vary stochastically.
One gramme of fresh material was fixed by boiling water for 5 min, in order to inactivate the phospholipases.
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