Microwave dosimeter - A concept

Dosimeter determines time-integrated radiation dosage to which an individual is exposed. Integration is measured chemically in proportion to radiation detected. Wearer receives an exposure measurement representing an average of the dose over the entire body

Evidence from Rb–Sr mineral ages for multiple orogenic events in the Caledonides of Shetland, Scotland

Shetland occupies a unique central location within the North Atlantic Caledonides. Thirty-three new high-precision Rb–Sr mineral ages indicate a polyorogenic history. Ages of 723–702 Ma obtained from the vicinity of the Wester Keolka Shear Zone indicate a Neoproterozoic (Knoydartian) age and preclude its correlation with the Silurian Moine Thrust. Ordovician ages of c. 480–443 Ma obtained from the Yell Sound Group and the East Mainland Succession constrain deformation fabrics and metamorphic assemblages to have formed during Grampian accretionary orogenic events, broadly contemporaneously with orogenesis of the Dalradian Supergroup in Ireland and mainland Scotland. The relative paucity of Silurian ages is attributed to a likely location at a high structural level in the Scandian nappe pile relative to mainland Scotland. Ages of c. 416 and c. 411 Ma for the Uyea Shear Zone suggest a late orogenic evolution that has more in common with East Greenland and Norway than with northern mainland Scotland

Absorbance of the OH Radical in a Specific Wavelength Interval Near 309A

The absorbance of the OH radical as a function of optical density was studied by computing the absorbance for an incident radiation in the wavelength interval 3089A-3097A. The absorbance was studied for 3 different temperatures and various values of the parameters specifying the line shapes and magnitude of the spectral absorption coefficient

Mbd1 is recruited to both methylated and nonmethylated CpGs via distinct DNA binding domains

MBD1 is a vertebrate methyl-CpG binding domain protein (MBD) that can bring about repression of methylated promoter DNA sequences. Like other MBD proteins, MBD1 localizes to nuclear foci that in mice are rich in methyl-CpG. In methyl-CpG-deficient mouse cells, however, Mbd1 remains localized to heterochromatic foci whereas other MBD proteins become dispersed in the nucleus. We find that Mbd1a, a major mouse isoform, contains a CXXC domain (CXXC-3) that binds specifically to nonmethylated CpG, suggesting an explanation for methylation-independent localization. Transfection studies demonstrate that the CXXC-3 domain indeed targets nonmethylated CpG sites in vivo. Repression of nonmethylated reporter genes depends on the CXXC-3 domain, whereas repression of methylated reporters requires the MBD. Our findings indicate that MBD1 can interpret the CpG dinucleotide as a repressive signal in vivo regardless of its methylation status