The mean cross-section diameter of axons with DAT-Type I immunolabeling was 0.13 μm (SD = 0.04), their mean perimeter was 0.81 μm (SD = 0.29), and mean surface area was 0.04 μm (SD = 0.02).
The mean diameter of axons with DAT-Type II immunolabeling was 0.16 μm (SD = 0.07), their mean perimeter was 0.96 μm (SD = 0.50), and mean surface area was 0.06 μm (SD = 0.06).
The mean diameter of axons with DAT-Type III immunolabeling was 0.17 μm (SD = 0.06), their mean perimeter was 0.88 μm (SD = 0.34), and mean surface area was 0.05 μm (SD = 0.03).
In addition, the total neuron (intact) numbers and mean surface area were decreased.
Critical micelle concentration (CMC), average minimal surface tension (γCMC), saturated surface excess (Γm), mean surface area per molecule (S), and adsorption efficiency (pC20) were determined from the surface tension profiles and compared for the three surfactant systems.
The mean surface area per cell was found to be increased by three-fold (n = 3 assays, p < 0.01), for the cells plated on particles exposing RGD-peptides when compared to cells on control particles.
The suitable ethanol sensing characteristics of ZnO[nitrate] sample was explained by its highly porous structure as the mean surface area of the samples calculated from BET method followed from ZnO[nitrate] > ZnO[acetate] > ZnO[sulfate] sequence.
The mean surface area of glands per unit area of endometrium at the intercaruncular site in heifers and cows was approximately 18 mm2/mm2 in the follicular phase and 26 mm2/mm2 in the luteal phase, figures similar to the gland area found in women.
The mean surface area of the footprint of the cells was 98.94±4.42 µm2 and their average membrane capacitance was 8.19±0.21 pF, which corresponds to an average total surface area of 819±21 µm2 (assuming 1 µF·cm−2, Table 1, [16]).
