Can silicon monoxide grains be responsible for the interstellar 9.7 micrometer absorption band?

In this paper results of an experimental investigation of the spectra of submicrometersized silicon monoxide grains are presented. The grains manufactured from commercial SiO were prepared according to the Jena IR spectroscopy program for particulates of cosmic importance. The comparison of the laboratory spectra with those derived by means of Mie calculations using published refractive indices of bulk SiO revealed a fundamental discrepancy concerning the number and the positions of the bands. Therefore, the experimental SiO grains are suggested to change their internal structural state by the heating connected with the pressing of the KBr pellets, where the grains are embedded in. This sensitivity against heating by some hundred K rules out that SiO grains can be responsible for the 9.7 m circumstellar as well as interstellar spectral feature.     

On the detection of newly created CN radicals in comets

Laboratory investigations of CN radical formation by photodissociation of parent molecules have suggested the possibility of observing emission lines in cometary spectra from newly formed CN radicals. These laboratory studies have shown that high initial internal excitation of CN is the rule with excitation of rotational levels N up to 70. In the collisionless environment of the cometary atmosphere this initial excitation would yield a corresponding distribution for the lowest vibrational level of the ground X²Σ⁺ state. Our calculations show that it is feasible with present observational techniques to detect photochemically excited lines with N ～ 30 in the 0-0 band of the violet system.     

Qualitative study of the planar isosceles three-body problem

We consider the particular case of the planar three body problem obtained when the masses form an isosceles triangle for all time. Various authors [1, 2, 12, 8, 9, 13, 10] have contributed in the knowledge of the triple collision and of several families of periodic orbits in this problem. We study the flow on a fixed level of negative energy. First we obtain a topological representation of the energy manifold including the triple collision and infinity as boundaries of that manifold. The existence of orbits connecting the triple collision and infinity gives some homoclinic and heteroclinic orbits. Using these orbits and the homothetic solutions of the problem we can characterize orbits which pass near triple collision and near infinity by pairs of sequences. One of the sequences describes the regions visited by the orbit, the other refers to the behaviour of the orbit between two consecutive passages by a suitable surface of section. This symbolic dynamics which has a topological character is given in an abstract form and after it is applied to the isosceles problem. We try to keep globality as far as possible. This strongly relies on the fact that the intersection of some invariant manifolds with an equatorial plane (v=0) have nice spiraling properties. This can be proved by analytical means in some local cases. Numerical simulations given in Appendix A make clear that these properties hold globally.     

Non‐Matrix‐Matched Calibration for the Multi‐Element Analysis of Geological and Environmental Samples Using 200 nm Femtosecond LA‐ICP‐MS: A Comparison with Nanosecond Lasers

LA‐ICP‐MS is one of the most promising techniques for in situ analysis of geological and environmental samples. However, there are some limitations with respect to measurement accuracy, in particular for volatile and siderophile/chalcophile elements, when using non‐matrix‐matched calibration. We therefore investigated matrix‐related effects with a new 200 nm femtosecond (fs) laser ablation system (NWRFemto200) using reference materials with different matrices and spot sizes from 10 to 55 μm. We also performed similar experiments with two nanosecond (ns) lasers, a 193 nm excimer (ESI NWR 193) and a 213 nm Nd:YAG (NWR UP‐213) laser. The ion intensity of the 200 nm fs laser ablation was much lower than that of the 213 nm Nd:YAG laser, because the ablation rate was a factor of about 30 lower. Our experiments did not show significant matrix dependency with the 200 nm fs laser. Therefore, a non‐matrix‐matched calibration for the multi‐element analysis of quite different matrices could be performed. This is demonstrated with analytical results from twenty‐two international synthetic silicate glass, geological glass, mineral, phosphate and carbonate reference materials. Calibration was performed with the certified NIST SRM 610 glass, exclusively. Within overall analytical uncertainties, the 200 nm fs LA‐ICP‐MS data agreed with available reference values.     

Development of a Matrix‐Matched Sphalerite Reference Material (MUL‐ZnS‐1) for Calibration of In Situ Trace Element Measurements by Laser Ablation‐Inductively Coupled Plasma‐Mass Spectrometry

Sphalerite (ZnS) is an abundant ore mineral and an important carrier of elements such as Ge, Ga and In used in high‐technology applications. In situ measurements of trace elements in natural sphalerite samples using LA‐ICP‐MS are hampered by a lack of homogenous matrix‐matched sulfide reference materials available for calibration. The preparation of the MUL‐ZnS1 calibration material containing the trace elements V, Cr, Mn, Co, Ni, Cu, Ga, Ge, As, Se, Mo, Ag, Cd, In, Sn, Sb, Tl and Pb besides Zn, Fe and S is reported. Commercially available ZnS, FeS, CdS products were used as the major components, whereas the trace elements were added by doping with single‐element ICP‐MS standard solutions and natural mineral powders. The resulting powder mixture was pressed to pellets and sintered at 400 °C for 100 h using argon as an inert gas. To confirm the homogeneity of major and trace element distributions within the MUL‐ZnS1 calibration material, measurements were performed using EPMA, solution ICP‐MS, ICP‐OES and LA‐ICP‐MS. The results show that MUL‐ZnS‐1 is an appropriate material for calibrating trace element determination in sphalerite using LA‐ICP‐MS.     

Pedo‐Geochemical Signatures of Archeological Sites in the Tapirapé‐Aquiri National Forest in Marabá, Amazonia,Brazil

The present study aims to interpret the occupation of terra firme (nonflooded uplands) archeological sites located at Tapirapé‐Aquiri National Forest in the Brazilian state of Pará, through an integrated analysis of pedological, archeological, and geochemical data. We focus on seven archaeological sites, selected among 22 identified in the region. Radiocarbon and thermoluminescence dating indicate distinct periods of occupation over the past ∼6000 years, and the pedo‐geochemical data identify intra‐ and inter‐site differences in soil. Archaeological, chronometric, and pedo‐geochemical data provide a basis for the functional classification of archeological sites found in the region and help to identify specific human activity areas. The results lead us to infer that many of the archeological sites were the result of multiple occupations that left a persistent pedological signature on the landscape.     

GHG mitigation of agricultural peatlands requires coherent policies

As soon as peat soil is drained for agricultural production, the peat starts to degrade, which causes emissions to the atmosphere. In countries with large peatland areas, the GHG mitigation potential related to management of these soils is often estimated as the highest amongst the measures available in agriculture. Although the facts are well known, the policies leading to diminished emissions are often difficult to implement. We have analysed the reasons why the mitigation potential is not fully utilized and what could be done better in national implementation of climate policies. Four cases are used to illustrate the necessary steps to reach mitigation targets: determining the amount and properties of peat soils, estimating the potential, costs and feasibility of the mitigation measures, and selecting and implementing the best measures. A common feature for all of the cases was that national and international climate policies have increased the public interest in GHG emissions from peat soils and increased the pressure for mitigation. Basically the same factors restrict the implementation of mitigation measures in all countries with significant peat soil areas. The most important of these is lack of policy coherence, e.g. ignoring climate policies when planning land use or agricultural policies. We conclude that GHG mitigation is achieved only if other policies, especially national regulations and strategies, are in line with climate policies.

Policy relevance

Agricultural peat soils could be used to help reach GHG mitigation goals in many countries, but the full potential of mitigation of peat soils is not used. Although peatland cultivation inevitably leads to loss of the whole peat layer and high emissions, there are few incentives or regulation to effectively minimize these losses. This article discusses the possibilities to reduce GHG emissions from agricultural peat soils, with specific emphasis on the barriers of implementing mitigation measures nationally. The lessons learned from the selected cases emphasize the role of all policy makers and their cooperation in planning coherent policies for achieving the goals determined by climate policies.     

Seasonal variation of polychlorinated biphenyl concentrations in the southern part of the Baltic Sea

The impact of seasonal fluctuations in forcing factors such as atmospheric concentration, temperature, and biological productivity on the concentration of polychlorinated biphenyls (PCBs) in the surface water of the southern part of the Baltic Sea was investigated. Water samples were collected on eight cruises over 2 years. A clear seasonal variability in dissolved PCB concentrations was observed with higher levels in summer than in winter and spring. This was attributed to changes in atmospheric concentrations and water temperature, based on measurements showing the PCB levels in the atmosphere and surface water to be close to a partitioning equilibrium. Concentrations in the suspended particulate material (SPM) fraction were also variable, and when the quotient of the organic carbon normalised concentration in SPM and the dissolved concentration was calculated (i.e., the bioaccumulation factor (BAF)), a seasonal pattern was observed which was consistent with kinetic limitations on partitioning into particles caused by plankton growth. However, seasonal variability in the partitioning properties of the SPM may also contribute to this variability.