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The pore aperture distribution was evaluated from Hg-porosimetry determinations and the surface areas were determined using the B.E.T. method.
Both the average and critical cross-sectional areas were determined using a 3D laser scanner.
The specific surface areas were determined using the Brunauer Emmett Teller (BET) method with a Quantachrome NOVA 3000 Analyzer (USA).
The BET surface areas were determined using a Micromeritics ASAP 2010 N2 adsorption apparatus (Norcross, GA, USA).
In addition, priority areas were determined using an evaluation matrix and results showed that around 8.4% (193.4 ha) of LMW have high to very high priority levels.
Mensuration characteristics (volume, growing stock increment) of the studied samples of Scots pine at these seven forest areas were determined using the standard Russian methods (Chernykh et al. 2006).
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[11C]AF150(S) specific binding in M1ACh-R-rich brain areas was determined using SRTM with the cerebellum as reference tissue.
Determination of the support/catalyst porosity, pore volume, and surface area were determined using a Micromeritics ASAP 2000 N2-physisorption apparatus.
Cell viability, morphology, cytoskeleton architecture (microfilaments and microtubules), cell adhesion and migration into the scratch-wound area were determined using pristine graphene-coated microscopic slides.
Changes in tendon length, muscle belly dimensions (length, width, thickness), as well as aponeurosis length, width, and area were determined using 55 rabbits between 18 and 108 days old.
Vessel density and hypoxia area were determined using NIH image software as previously described [ 18].
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