Fe2+/Fe3+ ratios in bottom sediments of some lakes in British Columbia,Canada

Fe²⁺/Fe³⁺ ratio versus sediment depth values have been determined for ten lakes in British Columbia. The values often reflect the local topography of the lakes, the weathering history of the deposited minerals, and the diagenesis of the minerals after deposition in the lake.     

Analysis of fragrance compounds in blood samples of mice by gas chromatography, mass spectrometry, GC/FTIR and GC/AES after inhalation of sandalwood oil.

After inhalation experiments with sandalwood oil and the pure fragrance compounds coumarin and alpha-terpineol, substances were detected and measured in the blood samples of test animals (mice) using gas chromatography/mass spectrometry (GC/MS) (MID) in connection with GC/FTIR (SWC), GC/AES (carbon and oxygen trace) and flame ionization detection/gas chromatography. Using tiglinic acid benzyl ester as the internal standard the following concentrations in serum could be found: alpha-santalol 6.1 ng/mL, beta-santalol 5.3 ng/mL and alpha-santalene 0.5 ng/mL. In separate inhalation experiments with coumarin and with alpha-terpineol the corresponding concentrations were 7.7 ng/mL and 6.9 ng/mL, respectively.     

Ultrasonic wave propagation in cancellous and cortical bone: prediction of some experimental results by Biot's theory.

Pulse transmission ultrasound was used to determine the longitudinal wave speed along the direction of trabecular alignment in 32 water-saturated anisotropic tibial bovine cancellous bone samples and in one cortical bone sample also from the bovine tibia. These results are compared to published ultrasound wave-speed data obtained from bovine femoral specimens. Nonlinear regression was used to fit Biot's theory to the data. The correlation coefficient for regression analysis between the experimental ultrasound velocities and the velocities predicted by Biot's theory was r = 0.78.     

Likelihood Ratio Tests for Principal Components

A particular class of tests for the principal components of a scatter matrix Σ is proposed. In the simplest case one wants to test whether a given vector is an eigenvector of Σ corresponding to its largest eigenvalue. The test statistics are likelihood ratio statistics for the classical Wishart model, and critical values are obtained parametrically as well as nonparametrically without making any assumptions on the eigenvalues of Σ. Still, the tests have asymptotic properties similar to those of classical procedures and are asymptotically admissible and optimal in some sense.     

Synthesis of 1,3,4,6,7,11b-hexahydro[1,4]thiazino[3,4,-a]-isoquinolin-4-one,an analog of prasiquantel

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 994–996, July, 1992.     

On the resolving power of high-contrast saturated absorption spectroscopy

Recently Svanberg et al. [Optics Lett. 11 (1986) 138; J. Opt. Soc. Am. B 4 (1987) 462] obtained saturated absorption resonances with subnatural linewidth by working in the regime of high pumping intensities and optically thick atomic samples. We analyze here this new spectroscopic regime, within the formalism of Maxwell-Bloch-type equations, in the case of a Doppler broadened medium having two nearly degenerate but uncoupled resonances. We show that even in this most favourable case it is not possible to resolve spectral features that lie within the natural linewidth.     

Identification of metabolites of halofantrine, a new candidate anti-malarial drug, by gas chromatography-mass spectrometry.

Two previously unknown metabolites of halofantrine, a candidate anti-malarial drug, have been isolated by thin-layer chromatography from the plasma of dogs administered a single oral dose of 60 mg/kg. Their identifies were investigated after trimethylsilylation by gas chromatography-mass spectrometry under electron-impact and negative-ion chemical ionization conditions. The structural assignment was further confirmed by using a combination of elemental composition analysis of all the isotope peaks at low mass resolution and isotope pattern matching. These two metabolites were formed by modification of the dibutylaminopropyl side-chain of the parent compound involving deamination and oxidation or reduction.