Microlite orientation in obsidian flow measured by synchrotron X-ray diffraction

Clinopyroxene and plagioclase (andesine) microlites in an obsidian flow from Glass Mountain (NE California, USA) display strong alignment. Synchrotron X-ray diffraction, coupled with Rietveld analysis, was used to quantify crystallographic-preferred orientation (CPO). Clinopyroxene, with a rod-shaped morphology, shows a strong alignment of [001] in the flow direction and (010) aligned parallel to the inferred flow plane. Andesine, with a platy morphology, displays an alignment of (010) platelets in the flow plane. Some pole densities exceed 90 multiples of random distribution. Applying a model of rigid ellipsoidal inclusions in a viscous matrix, the local pure shear strains are between 2 and 3

Vitamin E content of different animal products: Influence of animal nutrition

Zusammenfassung: In der vorliegenden Studie wurde der α-Tocopherolgehalt verschiedener Fleischstücke untersucht. Hähnchenschenkel hatte den höchsten α-Tocopherolgehalt, gefolgt von Hähnchenbrust und Schweineschulter (p Leber > Fettgewebe >Musculus longissimus dorsi. Die Nährstoffdichten betrugen 28.8, 7.3, 0.9 und 1.2 mg α-Tocopherol/MJ für Eigelb, Leber, Fettgewebe und Musculus longissimus dorsi der jeweiligen mit Vitamin E supplementierten Gruppe. Diese Ergebnisse zeigen, daß Fleisch, mit Ausnahme des Hähnchenschenkels, von Tieren mit supplementierten Diäten kein bedeutender Vitamin E-Lieferant ist. Hingegen wurde Eigelb durch fütterungsbedingte Modifikation zu einer guten Vitamin E-Quell

Plasma concentration monitoring of aminoglycosides

A narrow therapeutic margin and poor predictability of plasma concentrations are the main reasons for drug level monitoring during aminoglycoside treatment. Gentamicin, tobramycin, amikacin and netilmicin can now be accurately and rapidly measured by radioenzymic, radio-immuno and enzyme-immuno assays. Routine determinations of peak (1-2 h post dose) and trough levels are recommended to ensure adequate dosage in all patients with serious Gram-negative infections, especially when renal function is impaired. It should be realized, however, that maintaining aminoglycoside concentrations within a given range will only reduce, but not entirely eliminate the risk of toxicity. The pharmaco kinetic behaviour of these antibiotics leads to a progressive drug accumulation in renal tissue and the inner ear, which depends both on dosage amd duration of treatment. Une marge thérapeutique étroite ainsi que la difficulté a prédire les concentration plasmatiques, sont les principales raisons de contrôle des taux sanguins au cours d'un traitement par les aminoglycosides. Aujourd'hui les concentrations de gentamicine, tobramycine, amikacine et nétilmicine peuvent ětre mesurées rapidement et de manière précise par les méthodes radio-enzymatiques, radio immunologiques et enzymo-immunologiques. La détermination du pic (1 à 2 heures après administration) et du taux résiduel est recommandée pour assurer un dosage adéquat chez tous les malades atteints d'une infection sevère à germes Gram-négatif, et particulièrement en cas d'insuffisance rénale. Il faut pourtant bien garder à l'esprit, que le fait de maintenir la concentration d'une aminoglycoside à un niveau donné, permet seulement de diminuer les risques de toxicité, mais pas de les éliminer totalement. La pharmacocinétique particulière de ces antibiotiques entraine une accumulation progressive dans le parenchyme renal et dans l'oreille interne, qui depend à la fois de la posologie et de la durée du traitemen

Reply to “Comment on ‘Temperature-dependent orientational ordering on a spherical surface modeled with a lattice spin model’ ”

A reply to the comment of S. Romano, Phys. Rev. E 2015 on our previous paper is provided

Regional wave propagation using the discontinuous Galerkin method

We present an application of the discontinuous Galerkin (DG) method to regional wave propagation. The method makes use of unstructured tetrahedral meshes, combined with a time integration scheme solving the arbitrary high-order derivative (ADER) Riemann problem. This ADER-DG method is high-order accurate in space and time, beneficial for reliable simulations of high-frequency wavefields over long propagation distances. Due to the ease with which tetrahedral grids can be adapted to complex geometries, undulating topography of the Earth's surface and interior interfaces can be readily implemented in the computational domain. The ADER-DG method is benchmarked for the accurate radiation of elastic waves excited by an explosive and a shear dislocation source. We compare real data measurements with synthetics of the 2009 L'Aquila event (central Italy). We take advantage of the geometrical flexibility of the approach to generate a European model composed of the 3-D <i>EPcrust</i> model, combined with the depth-dependent <i>ak135</i> velocity model in the upper mantle. The results confirm the applicability of the ADER-DG method for regional scale earthquake simulations, which provides an alternative to existing methodologies

Effect of Pelleting Temperature on the Activity of Different Enzymes

The effects of different pelleting temperatures on the activity of cellulase, bacterial amylase, fungal amylase, and pentosanase were tested. Samples of a commercial barley-wheat-soybean diet containing different enzyme preparations were pelleted at 60, 70, 80, 90, and 100 C (pellet temperature measured at the die outlet) through a die containing holes 2.5 mm in diameter. Enzymatic analyses were conducted on either soluble substrates or by measuring the ability of the tested enzymes to decrease the viscosity of the diet. Measurements made on soluble substrates suggest that cellulase, fungal amylase, and pentosanase maintained activity when being pelleted at temperatures up to 80 C and bacterial amylase maintained activity at temperatures up to 90 C. Pentosanase and amylases showed little or no effect on the viscosity of the diet. Cellulase addition decreased the viscosity at all temperature levels, even after being pelleted at 90 and 100 C (P < 0.05). No cellulolytic activity was detected on the soluble substrate after these pelleting temperatures. Measurements on a soluble substrate might therefore not always reflect the true stability of a preparation because the ability of a carbohydrase to decrease the viscosity of the digesta is important to its effect in the gastrointestinal tract. Measurements on soluble substrates suggest that cellulase, fungal amylase, and pentosanase can be pelleted at temperatures up to at least 80 C and bacterial amylase up to 90 C without a considerable loss in analyzed activit

Monographies on drugs, which are frequently analysed in the course of Therapeutic Drug Monitoring Monographien über Medikamente, die regelmässig im Rahmen des Therapeutic Drug Monitorings analysiert werden

In 1995 the working group "Drug Monitoring” of the Swiss Society of Clinical Chemistry (SSCC) has already published a printed version of drug monographs, which are now newly compiled and presented in a standardised manner. The aim of these monographs is to give an overview on the most important informations that are necessary in order to request a drug analysis or is helpful to interpret the results. Therefore, the targeted audience are laboratory health professionals or the receivers of the reports. There is information provided on the indication for therapeutic drug monitoring, protein binding, metabolic pathways and enzymes involved, elimination half life time and elimination routes as well as information on therapeutic or toxic concentrations. Because preanalytical considerations are of particular importance for therapeutic drug monitoring, there is also information given at which time the determination of the drug concentration is reasonable and when steady-state concentrations are reached after changing the dose. Furthermore, the stability of the drug and its metabolite(s), respectively, after blood sampling is described. For readers with a specific interest, references to important publications are given. The number of the monographs will be continuously enlarged. The updated files are presented on the homepage of the SSCC (www.sscc.ch). We hope that these monographs are helpful for you handling therapeutic drug monitoring and look forward to comments of the audienc