Climate Change driven evolution of hazards to Europe’s transport infrastructure throughout the twenty-first century

Air circulation due to the urban heat island (UHI) effect can influence the dispersion of air pollutants in a metropolis. This study focusses on the influence of the UHI effect on particulate matter (PM; including PM_2.5 and PM_2.5–10) between May and September 2010–2012 in the Taipei basin. Meteorological and PM data were obtained from the sites, owned by the governmental authorities. The analysis was carried out using t test, relative indices (RIs), Pearson product–moment correlation and stepwise regression. The results show that the RI values for PM were the highest at moderate UHI intensity (MUI; 2 °C ≤ UHI < 4 °C) rather than at strong UHI intensity (SUI; 4 °C ≤ UHI) during the peak time for anthropogenic emissions (20:00 LST). Neither the accumulation of PM nor the surface convergence occurred in the hot centre, as shown by the case study. At MUI, more than 89 % of the synoptic weather patterns showed that the weather was clear and hot or that the atmosphere was stable. The variation in PM was associated with horizontal and vertical air dispersion. Poor horizontal air dispersion, with subsidence, caused an increase in PM at MUI. However, the updraft motion diluted the PM at SUI. The stepwise regression models show that the cloud index and surface air pressure determined the variation in PM_2.5–10, while cloud index, wind speed and mixing height influenced the variation in PM_2.5. In conclusion, a direct relationship between UHI effect and PM was not obvious.     

High-Precision Trace Element Data for the USGS Reference Materials BCR-1, BCR-2, BHVO-1, BHVO-2, AGV-1, AGV-2, DTS-1, DTS-2, GSP-1 and GSP-2 by ID-TIMS and MIC-SSMS

Different batches of the new US Geological Survey (USGS) reference materials (RMs) BCR-2, BHVO-2, AGV-2, DTS-2 and GSP-2 and the original USGS RMs BCR-1, BHVO-1, AGV-1, DTS-1 and GSP-1 have been analysed by isotope dilution using thermal ionisation mass spectrometry (ID-TIMS) and by multi-ion counting spark source mass spectrometry (MIC-SSMS). The concentrations of K, Rb, Sr, Ba and the rare earth elements were determined with overall analytical uncertainties of better than 1% (ID-TIMS) and 3% (MIC-SSMS). The analyses of different aliquots and batches of BCR-2, BHVO-2, AGV-2 and GSP-2, respectively, agree within 1%, i.e. approximately the analytical uncertainties of the data. This indicates an homogeneous distribution of the trace elements in these RMs. Differences in element concentrations of up to 17% in different aliquots of the depleted RM DTS-2 are outside the analytical uncertainty of our data. They may be attributed to a slightly heterogeneous distribution of trace elements in this dunite sample. Our trace element data for BCR-2, BHVO-2, AGV-2 and GSP-2 agree within about 3% with preliminary reference values published by the USGS. They also agree within 1-6% with those of the original RMs BCR-1, BHVO-1, AGV-1 and GSP-1. Large compositional differences are found between DTS-2 and DTS-1, where the concentrations of K, Rb, Sr and the light REE differ by factors of 2 to 24.     

Potential for remediation of acidic mining lakes evaluated by hydrogeochemical modelling: Case study Grünewalder Lauch (Plessa 117, Lusatia/Germany)

About one third of several hundred mining lakes in Eastern Germany are highly acidified, and there is a need to restore them to neutral conditions because they constitute an environmental hazard for water resources and downstream environments. The aim of this study is to evaluate the efficiency of three different acid pit lake water remediation treatments: dilution with alkaline (river) water, limestone treatment and biological neutralization by organic carbon-driven alkalinity generation. The efficiency is evaluated for the acidic mining lake Grünewalder Lauch by adjusting input values into a geochemical model and making future projections. Current approaches, such as flooding with neutral surface water or extensive liming, are not suitable for many lakes because of a limited supply of alkaline water or high lime immobilizing potential of Fe- and Al-rich water in acidic lakes, respectively. Further treatment methods are, therefore, designed to combine water supply and biological measures with the management of water quality by the application of in-lake microbial processes. These processes are focused on the metabolic response of aquatic ecosystems to nutrient enrichment (enhancement of primary production and thereby organic carbon supply) and the microbial decomposition of organic matter and their effects on the gain or loss of alkalinity.The results and comparisons of different neutralization measures will be generalized by the application of hydrogeochemical models for alkalinity production showing

a)

the long term efficiency of the measures, depending on carbon turnover at the sediment/water interface,

b)

the development of bicarbonate buffering capacity as a consequence of biological measures,

c)

the importance of pyrite formation instead of FeS.

     

Reference Values Following ISO Guidelines for Frequently Requested Rock Reference Materials

We present new reference values for nineteen USGS, GSJ and GIT‐IWG rock reference materials that belong to the most accessed samples of the GeoReM database. The determination of the reference values and their uncertainties at the 95% confidence level follows as closely as possible ISO guidelines and the Certification Protocol of the International Association of Geoanalysts. We used analytical data obtained by the state‐of‐the‐art techniques published mainly in the last 20 years and available in GeoReM. The data are grouped into four categories of different levels of metrological confidence, starting with isotope dilution mass spectrometry as a primary method. Data quality was checked by careful investigation of analytical procedures and by the application of the Horwitz function. As a result, we assign a new and more reliable set of reference values and respective uncertainties for major, minor and a large group of trace elements of the nineteen investigated rock reference materials.     

Circumstellar aluminum oxide and silicon carbide in interplanetary dust particles

A systematic NanoSIMS isotope imaging study of sub-micrometer phases in interplanetary dust particles (IDPs) has led to the discovery of two presolar grain types that previously were observed only in primitive meteorites. A 350 × 600 nm² Al₂O₃ grain has a large ¹⁷O enrichment and a slight ¹⁸O depletion, as well as a ²⁶Mg excess due to the decay of extinct ²⁶Al. Because of its relatively large size and prominent location within the IDP, this presolar Al₂O₃ grain is well characterized by SEM-EDX analyses. A second, much smaller presolar grain has a diameter of 150 nm and a ¹³C enrichment of more than 300%. Isotopic anomalies in C are rarely found in IDPs and the magnitude of this anomaly is unprecedented. This grain also has a ¹⁵N-rich composition and its isotopic makeup as well as its secondary ion yields identify it as a SiC grain. The discovery of presolar Al₂O₃ and SiC in IDPs seamlessly complements earlier notions of interplanetary dust particles as the most primitive extraterrestrial material currently available for laboratory analysis. Both Al₂O₃ and SiC are common presolar grain types in primitive meteorites, but they appeared conspicuously absent from the presolar grain inventory in interplanetary dust particles, which is dominated by silicate stardust. Not finding these presolar grain types in interplanetary dust would have been difficult to explain. Abundance estimates of the new presolar grain types in IDPs are hampered by limited statistics, but both Al₂O₃ and SiC are less common than presolar silicates which have been found at relatively high abundances in IDPs. The particle in which these presolar grains have been found belongs to the ‘isotopically primitive subgroup’ of IDPs, yet does not contain any presolar silicates.     

Long term mobilisation of chemical elements in tephra-rich peat (NE Iceland)

This paper presents geochemical profiles of a tephra-bearing minerotrophic peat column from NE-Iceland obtained using various elemental analyses of the solid phase and the pore water. The influence of tephra grain size, thickness and composition of each tephra on the peat geochemistry was investigated. Interpretations are supported by a statistical approach, in particular by autocorrelation, and by microscopy observations. Minerotrophic peat geochemistry may be strongly dependent upon post-depositional mobilization and possible leaching of elements as demonstrated by Fe and trace metal concentration profiles. Chemical elements, and more specifically potentially harmful metals, can be slowly leached out of volcanic falls during their weathering and re-accumulate downwards. It is emphasised that a tephra deposit can act as an active geochemical barrier, blocking downward elemental movements and leading to the formation of enriched layers. In this study, the formation of poorly amorphous Fe phases above the Hekla 3 tephra is shown. These poorly crystalline Fe phases scavenged Ni.     

Interstellar graphite in meteorites: Isotopic compositions and structural properties of single graphite grains from Murchison

Abstract— One hundred forty-three carbon grains, ranging in size from 2 to 8 μm, from two chemical and physical separates from the Murchison CM2 chondrite, were analyzed by ion microprobe mass spectrometry for their C- and N-isotopic compositions. Both separates are enriched in the exotic noble gas component Ne-E(L). Ninety grains were also analyzed for their H and O contents and 118, for Si. Thirteen grains were analyzed by micro-sampling laser Raman spectroscopy. Round grains have large C-isotopic anomalies with ¹²C/¹³C ratios ranging from 7 to 4500 (terrestrial ratio = 89). Nitrogen in these grains is also anomalous but shows much smaller deviations from the terrestrial composition, ¹⁴N/¹⁵N ratios ranging from 193 to 680 (terrestrial ratio = 272). Spherulitic aggregates and non-round compact grains have normal C-isotopic ratios but ¹⁵N excesses (up to 35%). Raman spectra of the analyzed grains indicate varying degrees of crystalline disorder of graphite with estimated in-plane crystallite dimensions varying from 18 Å (highly disordered, similar to terrestrial kerogen) to ～750 Å (well-crystallized graphite). Element contents of H, O, and Si are correlated with one another, and H and O are probably present in the form of organic molecules. On the basis of morphology, the round grains fall into two groups: grains with smooth, shell-like surfaces (“onions”) and grains that appear to be dense aggregates of small scales (“cauliflowers”). “Onions” tend to have lower trace element contents, isotopically light C (¹²C/¹³C > 89) and a high degree of crystalline order, whereas “cauliflowers” have a larger spread in trace element contents and C-isotopic ratios (they range from isotopically light to heavy) but tend to have a low degree of crystalline order. However, these differences exist only on average, and no clear distinction can be made for individual grains. A few limited conclusions can be drawn about the astrophysical origin of the carbon grains of this study. The ¹⁵N excesses in spherulitic aggregates and non-round grains can be explained as the result of ion-molecule reactions in molecular clouds. The round grains, on the other hand, must have formed in stellar atmospheres (circumstellar grains). Grains with isotopically light C must have formed in stellar environments characterized by He-burning, either in the atmosphere of Wolf-Rayet stars during the WC phase or in the He-burning, ¹²C-rich zone of a massive star, ejected by a supernova explosion. Isotopically heavy C is produced by H-burning in the CNO cycle. Possible sources for grains with heavy C are carbon stars (AGB stars during the thermally pulsing phase) or novae, but the detailed distribution of ¹²C/¹³C ratios agree neither with the distribution observed in carbon stars nor with theoretical predictions for these two types of stellar sources.     

Magnetic changes observed in the formation of two filaments in a complex active region: TRACE and MSDP observations

This paper is focused on the formation of two filaments in a complex center of decaying active regions (AR 8329 and AR 8326), located in the northern hemisphere. The observations were obtained in Hα by the Multi-channel Subtractive Double Pass spectrograph (MSDP mounted on the German telescope VTT in Tenerife) and EUV lines with TRACE (Transition Region And Corona Explorer). High Doppler shifts are found to be related to the ends of filament segments where canceling magnetic fields are also located (as seen on magnetograms from Big Bear Solar Observatory). At these locations, velocities along the line of sight, derived by using a cloud model method reach −20 km s⁻¹, the segments of filaments merge and frequently a time-related sub-flare is observed by TRACE. The chirality of the filament segments has been determined by different methods: the segments of dextral chirality join together and form a long dextral filament, and a single filament of sinistral chirality forms end to end with the dextral filament but does not merge with it. Assuming a model of twisted flux tube for filament material, we suggest that the dextral filament has negative helicity and a relationship between its formation and the close by sunspot with the same sign of helicity.     

The Preparation and Preliminary Characterisation of Eight Geological MPI-DING Reference Glasses for In-Situ Microanalysis

Eight silicate glasses were prepared by directly fusing and stirring 50-100 g each of basalt, andesite, komatiite, peridotite, rhyolite, and quartz-diorite. These are referred to as MPI-DING glasses and were made for the purpose of providing reference materials for geochemical, in-situ microanalytical work. Results from various analytical techniques indicate that individual glass fragments are well homogenised with respect to major and trace elements at the μm to mm scale. Heterogeneities due to quench crystallisation of olivine have been observed in small and limited areas of the two komatiitic glasses. In order to obtain concentration values for as many elements as possible, the glasses were analysed by a variety of bulk and microanalytical methods in a number of laboratories. The analytical uncertainties of most elements are estimated to be between 1% and 10%. From the analytical data, preliminary reference values for more than sixty elements were calculated. The analytical uncertainties of most elements are estimated to be between 1% and 10%.