Upward movement of tritium from contaminated groundwaters: a numerical analysis.

This paper describes a research-oriented modelling exercise that addresses the problem of assessing the movement of tritium from a contaminated perched aquifer to the land surface. Participants were provided with information on water table depth, soil characteristics, hourly meteorological and evapotranspiration data. They were asked to predict the upward migration of tritium through the unsaturated soil into the atmosphere. Eight different numerical models were used to calculate the movement of tritium. The modelling results agree within a factor of two, if very small time and space increments are used. The agreement is not so good when the near-surface soil becomes dry. The modelling of the alternate upward and downward transport of tritium close to the ground surface generally requires rather complex models and detailed input because tritium concentration varies sharply over short distances and is very sensitive to many interactive factors including rainfall amount, evapotranspiration rate, rooting depth and water table position.

Rapid determination of methandrostenolone in equine urine by isotope dilution liquid chromatography-tandem mass spectrometry.

Urine samples were spiked with [17-methyl-2H3]methandrostenolone as internal standard and extracted with a mixture of dichloromethane and cyclohexane. The organic phase was concentrated and injected onto a short octyl-silica column (30 mm x 4.6 mm I.D.) for separation of methandrostenolone and 17-epimethandrostenolone. The effluent from the column was connected to a Sciex TAGA 6000E triple quadrupole mass spectrometer equipped with an atmospheric pressure ion source for sampling of ions generated by a heated pneumatic nebulizer with corona discharge ionization. This ion source produced abundant [M + H]+ ions and a weak fragment ion due to loss of water. The protonated molecular ions at m/z 301 and 304 for methandrostenolone, 17-epimethandrostenolone and the internal standard were transmitted to the second quadrupole for collision-induced dissociation. Quantification was obtained by selected reaction monitoring of three daughter ions. Methandrostenolone and 17-epimethandrostenolone were separated by liquid chromatography, but gave identical mass spectra. The method detection limit by injection of a urine extract corresponding to 2.8 ml urine was 180 pg/ml at the 99% confidence level. The precision (relative standard deviation) was 3% at the 16 ng/ml level and the linear dynamic range was at least 3 orders of magnitude. Screening for unknown metabolites in urine after administration of methandrostenolone to horses and humans was accomplished by a parent ion scan of m/z 121, a fragment corresponding to the intact A-ring of the steroids.