In this paper we present data from the measurements of carbon isotopes (Δ14C and δ13C) from α-cellulose extracted from pine tree-rings. The samples were collected in four forests located in the most industrialized part of Poland, where coal mining and coal-based energy are an important branch of industry. The investigated period of time (1975–2012) covers the period of development in coal mining and other industry sectors. Stable isotope composition has been determined with using IRMS and radiocarbon concentration was determinate by AMS.

The Gaia astrometric reference catalogue will provide star proper motions with an accuracy of one mas one century ago for stars of magnitude 14 or brighter. Our project is to re-reduced the old observations with the new catalogue allowing to have an astrometric accuracy only limited by the observational biases and not by reference stars. Then, we plan to get an accuracy of 50 mas where the old reductions were not better than 500 mas!

For our purpose, we will digitize old photographic plates with a sub-micrometric scanner. Tests were made using the UCAC catalogue showing that old photographic plates have an intrinsect accuracy of 30 to 60 mas.

Techniques enabling in situ elemental and mineralogical analysis on extraterrestrial planets are strongly required for upcoming missions and are being continuously developed. There is ample need for quantitative and high-sensitivity analysis of elemental as well as isotopic composition of heterogeneous materials. Here we present in situ spatial and depth elemental profiles of a heterogeneous rock sample on a depth-scale of nanometres using a miniaturized laser ablation mass spectrometer (LMS) designed for planetary space missions. We show that the LMS spectra alone could provide highly detailed compositional, three-dimensional information and oxidation properties of a natural, heterogeneous rock sample. We also show that a combination of the LMS and Raman spectroscopy provide comprehensive mineralogical details of the investigated sample. These findings are of great importance for future space missions where quick, in situ determination of the mineralogy could play a role in the process of selecting a suitable spot for drilling.

In order to study the vertical migration of anthropogenic 137Cs, soil inventories ofthis radionuclide were measured in two regions selected on the basisof a previous comprehensive survey in the northern Iranian provinceof Guilan located in the South Caspian region. Ten sampling stations were randomly chosen in these regions and split-level samplingwas carried out to a depth of 30 cm. Sample analysis was performedusing a HPGe detector system. In situ gamma measurementsin both regions were als o carried out with the aid of a portable germanium spectrometer.The experimental data were then compared with the solution of theconvection-dispersion equation (CDE) with the proper initial and boundary conditions to evaluate initialdeposition as well as transport parameter values. The solution,including the effects of both considered sources, i.e. global falloutand Chernobyl releases, fits the measured data well. The effectiveconvection velocity and dispersion coefficients of 137Cslie in the range of 0-0.25 cm·y-1 and 0.32-0.75 cm2·y-1, respectively, indicating a very slow migration rate in the area. Most of the deposited 137Cs still remainedin the top 10-cm layer. Moreover, the fitted depth profiles werethen employed to correct the surface activities of 137Csestimated by in situ measurements.

La mise en œuvre des concepts de seuil de décision et de limite de détection pose souventdes problèmes aux métrologues des laboratoires d’analyse de biologie médicale chargés dela surveillance des salariés exposés aux rayonnements ionisants. Les problèmes mis enavant sont souvent relatifs au choix à faire entre diverses formules, dont les résultatsnumériques présentent cependant rarement des différences significatives. Les raisons plusprofondes des difficultés rencontrées sont en fait d’une part la signification etl’interprétation de ces tests statistiques, et d’autre part les valeurs utilisées dans cesformules parmi lesquelles l’estimation du bruit de fond reste la grandeur essentielle etla plus délicate à définir. L’objectif de ce premier article est de revenir dans unpremier temps sur les fondements des concepts de seuil de décision et de limite dedétection, en distinguant d’une part la méthode de détermination du seuil de décision basésur un risque d’erreur a priori de première espèce, d’autre partl’interprétation du résultat après mesure de l’échantillon. Nous exposerons ensuitequelques exemples d’optimisation de ces seuils et limites en spectrométrie gamma, où nousverrons que tout repose sur la recherche de la meilleure estimation possible du bruit defond qui nécessite bien plus une maitrise de la mesure que des outils de statistique. Unsecond article, mettant en œuvre les principes exposés ici, sera plus particulièrementconsacré à la démarche d’optimisation des seuils de décision en spectrométrie alpha pourles dosages d’uranium dans les urines.

Two recent developments in X-ray spectrometer technology provide dramatic improvements in analytical capabilities that impact the frontiers of electron microscopy. Silicon drift detectors (SDD) use the same physics as silicon (lithium) energy dispersive spectrometers [Si(Li) EDS] but differ in design: only 10% of the thickness of the Si(Li) EDS with an anode area below 0.1 mm2 and a complex rear surface electrode pattern that creates a lateral internal charge collection field. The SDD equals or betters the Si(Li) EDS in most measures of performance. For output versus input count rate, the SDD exceeds the Si(Li) EDS by a factor of 5 to 10 for the same resolution. This high throughput can benefit analytical measurements that are count limited, such as X-ray mapping and trace measurements. The microcalorimeter EDS determines the X-ray energy by measuring the temperature rise in a metal absorber. Operating at 100 mK, the microcalorimeter EDS achieves resolution of 2–5 eV over a photon energy range of 200 eV to 10 keV in energy dispersive operation, eliminating most peak interference situations and providing high peak-to-background to detect low fluorescence yield peaks. Chemical bonding effects on low energy (<2 keV) peak shapes can be measured.

Background: The cause of ossicular prosthesis extrusion remains an issue of interest to many otologists. This study evaluated the change in material surfaces and chemical elements of extruded total ossicular replacement prostheses (TORPs) and partial ossicular replacement prostheses (PORPs).

Methods: A total of nine extruded Polycel® ossicular prostheses (four TORPs, five PORPs) from nine patients was investigated using scanning electron microscope and energy dispersive X-ray spectrometry (EDX). Three prostheses (TORPs) obtained during revision surgery for hearing restoration were used as control subjects for EDX study.

Results: All subjects from the study group showed loss of fibrous capsule at both platform and shaft in the extruded prostheses. In comparison with the control group, the extruded prostheses had a lower level of carbon element (Wilcoxon signed-rank test, p < 0.05).

Conclusion: Loss of fibrous capsule and micro-degradation are probably two of the many factors that contribute to the extrusion of ossicular prostheses.

A technique has been developed for the interpretation of composition-depth profiles from angleresolved X-ray data using a Monte Carlo electron scattering simulation. This is a nondestructive depth profiling procedure. Software has been developed that uses a Monte Carlo scattering simulation to generate the signal intensity from a multilayer sample for any combination of primary beam angle of incidence and take-off angle to the X-ray detector. An interactive C++ application uses this simulation to interpret measured angle-resolved depth profiles. The method has been tested using a custom-made Ag/Al “staircase” sample containing two layers each of Ag and Al. Using the technique, it is possible to quantify the composition-depth profile for the two- and three-layer “steps” of the sample. Qualitative information may be gained about the four-layer area of the sample.

As Si(Li) detector technology has matured, many of the fundamental problems have been addressed in the competition among manufacturers and there is now an expectation, implied by many textbooks, that all energy-dispersive X-ray (EDX) detectors are made and will perform in the same way. Although there has been some convergence in Si(Li) systems and these are still the most common, manufacturing recipes still differ and there are many alternative EDX devices, such as microcalorimeters and room temperature detectors, that have both advantages and disadvantages over Si(Li). Rather than emphasizing differences in technologies, performance measures should reveal benefits relevant to the intended application. The instrument is inevitably going to be a “black box” of integrated components; this article reviews some of the methods that have been applied and introduces some new techniques that can be used to assess performance without resorting to complex software or sophisticated mathematical algorithms. Sensitivity, resolution, artefacts, and stability are discussed with particular application to compositional analysis using electron beam excitation of X-rays in the 100-eV to 10-keV energy region.