A simple spectrophotometric method is proposed for the simultaneous quantification of the ozone (O3) and hydrogen peroxide (H2O2) mixture, the so-called peroxone. This method is based on the measurements of the absorbance of the I3- produced by the oxidation of I- by peroxone. The oxidation rates of I- by O3 and H2O2 are largely different and pH-dependent and, moreover, the oxidation of I- by H2O2 can be accelerated by a molybdate catalyst. In addition, the present method was successfully applied at concentrations as low as 10μM for the analysis of a real peroxone sample prepared by electrolysis of water. © Taylor & Francis Group, LLC.

The oxidation reaction of triiodide, I3-, by chlorate is investigated in a slightly acidic and neutral media. The reaction was verified and monitored both potentiometrically and spectrophotometrically. Generally, a slow linear decay preceded by an induction period was observed for the triiodide concentration following the addition of chlorate. The induction period is likely to be related to the time required for the generation of suitable concentrations of plausible intermediates (HIO and HIO2), which are assumed to auto-catalyse the reaction. We examined the effect of acidity and concentrations of both chlorate and triiodide on the induction time for this reaction. The acidity of the medium influenced the induction period, while the oxidation of iodide by chlorate competed with that of iodine as the medium acidity increased, making the reaction more complicated. Therefore, a suitable pH is highly recommended for studying the chlorate-triiodide reaction. A plausible mechanism involving the HIO, HIO2, and I2O species is proposed. © 2010 Cairo University.

Introduction: The aim of this study was to assess the use of 3-dimensional facial averages for determining morphologic differences from various population groups. Methods: We recruited 473 subjects from 5 populations. Three-dimensional images of the subjects were obtained in a reproducible and controlled environment with a commercially available stereo-photogrammetric camera capture system. Minolta VI-900 (Konica Minolta, Tokyo, Japan) and 3dMDface (3dMD LLC, Atlanta, Ga) systems were used. Each image was obtained as a facial mesh and orientated along a triangulated axis. All faces were overlaid, one on top of the other, and a complex mathematical algorithm was performed until average composite faces of 1 man and 1 woman were achieved for each subgroup. These average facial composites were superimposed based on a previously validated superimposition method, and the facial differences were quantified. Results: Distinct facial differences were observed among the groups. The linear differences between surface shells ranged from 0.37 to 1.00 mm for the male groups. The linear differences ranged from 0.28 and 0.87 mm for the women. The color histograms showed that the similarities in facial shells between the subgroups by sex ranged from 26.70% to 70.39% for men and 36.09% to 79.83% for women. The average linear distance from the signed color histograms for the male subgroups ranged from -6.30 to 4.44 mm. The female subgroups ranged from -6.32 to 4.25 mm. Conclusions: Average faces can be efficiently and effectively created from a sample of 3-dimensional faces. Average faces can be used to compare differences in facial morphologies for various populations and sexes. Facial morphologic differences were greatest when totally different ethnic variations were compared. Facial morphologic similarities were present in comparable groups, but there were large variations in concentrated areas of the face. © 2010 American Association of Orthodontists.

Regions required for chicken glycine decarboxylase gene transcription were examined. A region between -82 and +22 (-82/+22) with motifs similar to binding sites for Sp1, NF-Y and CP2 was assigned to the proximal promoter active in both chicken hepatoma cell line, LMH, and hepatocytes in primary culture. In LMH cells, a genomic region, KX, between KpnI (-4155) and XbaI (-2113) sites changed promoter activity with the aid of four additional genomic regions termed upstream regulator regions for suppression (UpRS) and activation (UpRA) of transcription. Those precise segments are UpR1S (-376/-346), UpR1A (-345/-291), UpR2S (-137/-108) and UpR2A (-107/-83). Within KX, -4155/-3605 activates and -3604/-3367 suppresses the promoter. -3366/-3024 activates or suppresses the promoter, probably with different UpR counterparts. -2197/-2113 restores the actions of -3366/-3024. While in LMH cells, the upstream UpRs abrogate the functions of immediately downstream UpRs, UpR1S or UpR2S or both may be at least less active in hepatocytes than in LMH cells. Nuclear extracts from various chicken tissues and LMH cells had UpR2A binding proteins in different populations, suggesting that together with the UpRs, the segments in KX are involved in the regulation of cell type-specific transcription of this gene.

n/a