Area-Averaged Surface Fluxes Over the Litfass Region Based on Eddy-Covariance Measurements

Micrometeorological measurements (including eddy-covariance measurements of the surface fluxes of sensible and latent heat) were performed during the LITFASS-2003 experiment at 13 field sites over different types of land use (forest, lake, grassland, various agricultural crops) in a 20 × 20 km² area around the Meteorological Observatory Lindenberg (MOL) of the German Meteorological Service (Deutscher Wetterdienst, DWD). Significant differences in the energy fluxes could be found between the major land surface types (forest, farmland, water), but also between the different agricultural crops (cereals, rape, maize). Flux ratios between the different surfaces changed during the course of the experiment as a result of increased water temperature of the lake, changing soil moisture, and of the vegetation development at the farmland sites. The measurements over grass performed at the boundary-layer field site Falkenberg of the MOL were shown to be quite representative for the farmland part of the area. Measurements from the 13 sites were composed into a time series of the area-averaged surface flux by taking into account the data quality of the single flux values from the different sites and the relative occurrence of each surface type in the area. Such composite fluxes could be determined for about 80% of the whole measurement time during the LITFASS-2003 experiment. Comparison of these aggregated surface fluxes with area-averaged fluxes from long-range scintillometer measurements and from airborne measurements showed good agreement.     

Low-Level Atmospheric Jets And Inversions Over The Western Weddell Sea

For four months in the fall and earlywinter of 1992, as Ice Station Weddell (ISW) driftednorthward through the ice-covered western Weddell Sea,ice station personnel profiled the atmosphericboundary layer (ABL) with radiosondes. These showedthat the ABL was virtually always stably stratifiedduring this season: 96% of the soundings found anear-surface inversion layer. Forty-four percent ofthese inversions were surface-based. Eighty percentof the soundings that yielded unambiguous windprofiles showed an atmospheric jet with speeds as highas 14 m s^-1 in a core below an altitude of 425 m. This paper documents the features of these inversionsand low-level jets. Because the inversion statistics,in particular, are like those reported in and aroundthe Arctic Ocean, similar local processes seem tocontrol the ABL over sea ice regions in bothhemispheres. A simple two-layer model, in which anelevated layer becomes frictionally decoupled from thesurface, does well in explaining the ISW jetstatistics. This model also implies a new geostrophicdrag parameterization for sea-ice regions that dependson the magnitude of the geostrophic wind, the 10-mdrag coefficient C_DN10, and the ABL height, butnot explicitly on any stratification parameter.     

The Energy Balance Experiment EBEX-2000. Part I: overview and energy balance

An overview of the Energy Balance Experiment (EBEX-2000) is given. This experiment studied the ability of state-of-the-art measurements to close the surface energy balance over a surface (a vegetative canopy with large evapotranspiration) where closure has been difficult to obtain. A flood-irrigated cotton field over uniform terrain was used, though aerial imagery and direct flux measurements showed that the surface still was inhomogeneous. All major terms of the surface energy balance were measured at nine sites to characterize the spatial variability across the field. Included in these observations was an estimate of heat storage in the plant canopy. The resultant imbalance still was 10%, which exceeds the estimated measurement error. We speculate that horizontal advection in the layer between the canopy top and our flux measurement height may cause this imbalance, though our estimates of this term using our measurements resulted in values less than what would be required to balance the budget. The National Center for Atmospheric Research is supported by the National Science Foundation     

Determination of Reference Values for NIST SRM 610–617 Glasses Following ISO Guidelines

We present new reference values for the NIST SRM 610–617 glasses following ISO guidelines and the International Association of Geoanalysts’ protocol. Uncertainties at the 95% confidence level (CL) have been determined for bulk‐ and micro‐analytical purposes. In contrast to former compilation procedures, this approach delivers data that consider present‐day requirements of data quality. New analytical data and the nearly complete data set of the GeoReM database were used for this study. Data quality was checked by the application of the Horwitz function and by a careful investigation of analytical procedures. We have determined quantitatively possible element inhomogeneities using different test portion masses of 1, 0.1 and 0.02 μg. Although avoiding the rim region of the glass wafers, we found moderate inhomogeneities of several chalcophile/siderophile elements and gross inhomogeneities of Ni, Se, Pd and Pt at small test portion masses. The extent of inhomogeneity was included in the determination of uncertainties. While the new reference values agree with the NIST certified values with the one exception of Mn in SRM 610, they typically differ by as much as 10% from the Pearce et al. (1997) values in current use. In a few cases (P, S, Cl, Ta, Re) the discrepancies are even higher.     

Quantitative antimony speciation in shooting-range soils by EXAFS spectroscopy

The Sb speciation in soil samples from Swiss shooting ranges was determined using Sb K-edge X-ray absorption spectroscopy (XAS) and advanced statistical data analysis methods (iterative transformation factor analysis, ITFA). The XAS analysis was supported by a spectral data set of 13 Sb minerals and 4 sorption complexes. In spite of a high variability in geology, soil pH (3.1-7.5), Sb concentrations (1000-17,000 mg/kg) and shooting-range history, only two Sb species were identified. In the first species, Sb is surrounded solely by other Sb atoms at radial distances of 2.90, 3.35, 4.30 and 4.51 Å, indicative of metallic Sb(0). While part of this Sb(0) may be hosted by unweathered bullet fragments consisting of PbSb alloy, Pb L_III-edge XAS of the soil with the highest fraction (0.75) of Sb(0) showed no metallic Pb, but only Pb²⁺ bound to soil organic matter. This suggests a preferential oxidation of Pb in the alloy, driven by the higher standard reduction potential of Sb. In the second species, Sb is coordinated to 6 O-atoms at a distance of 1.98 Å, indicative of Sb(V). This oxidation state is further supported by an edge energy of 30,496-30,497 eV for the soil samples with <10% Sb(0). Iron atoms at radial distances of 3.10 and 3.56 Å from Sb atoms are in line with edge-sharing and bidentate corner-sharing linkages between Sb(O,OH)₆ and Fe(O,OH)₆ octahedra. While similar structural units exist in tripuhyite, the absence of Sb neighbors contradicts formation of this Fe antimonate. Hence the second species most likely consists of inner-sphere sorption complexes on Fe oxides, with edge and corner-sharing configuration occurring simultaneously. This pentavalent Sb species was present in all samples, suggesting that it is the prevailing species after weathering of metallic Sb(0) in oxic soils. No indication of Sb(III) was found.     

南极横贯南极山脉休斯陡崖花岗质岩体的成因

为了探讨横贯南极山脉休斯陡崖花岗质岩体的岩石成因,对其开展了岩相学和岩石化学分析。结果表明,休斯陡崖岩体主体岩石为二长花岗岩,后期被细粒二长花岗岩岩脉侵入。二者都具有高硅、富碱和高钾特征,里特曼指数小于3,岩石铝饱和指数(A/CNK)值小于1;微量元素原始地幔标准化分布型式具有Rb、Th、U和K元素富集,Nb、Ta、Nd和Ti等元素亏损特征;稀土元素总量偏低,轻稀土富集。主期二长花岗岩的稀土元素球粒陨石标准化分布型式具有轻微的负Eu异常,而岩脉具有正的Eu异常。休斯陡崖岩体的岩石类型为钙碱性准铝质I型花岗岩,源区为下陆壳,并伴有幔源物质的混入。在源区,岩浆发生了不同程度的斜长石、钛铁矿、金红石和磷灰石的分离结晶作用,其形成的构造环境为与俯冲作用有关的火山岛弧环境。      

Zirconolite and xenotime U–Pb age constraints on the emplacement of the Golden Mile Dolerite sill and gold mineralization at the Mt Charlotte mine,Eastern Goldfields Province,Yilgarn Craton,Western Australia

In situ SHRIMP U–Pb dating of magmatic zirconolite (CaZrTi₂O₇) in the Golden Mile Dolerite from the Mt Charlotte gold deposit (Yilgarn Craton, Australia) has yielded the first robust emplacement age (2,680 ± 9 Ma) for the principle host-rock of gold mineralization in the Kalgoorlie district. In contrast, co-magmatic zircon gave ages from ~2.68 Ga to ~2.17 Ga, reflecting isotopic resetting of high-U and -Th crystals. In situ SHRIMP analysis of hydrothermal xenotime (YPO₄), which co-exists with gold in alteration pyrite, provided a Pb/Pb isochron age of 2,655 ± 13 Ma. This date indicates that the youngest deposit in the Kalgoorlie district (Mt Charlotte) formed at ~2.65 Ga, and provides a new minimum age for the structurally older Golden Mile deposit. Our results indicate that gold mineralization at Mt Charlotte is ~50 million years older than indicated by recent ⁴⁰Ar/³⁹Ar dating and places new constraints on the timing of late-stage regional faulting (D₄) in the province.     

The Preparation and Preliminary Characterisation of Three Synthetic Andesite Reference Glass Materials (ARM‐1, ARM‐2, ARM‐3) for In Situ Microanalysis

Three synthetic reference glasses were prepared by directly fusing and stirring 3.8 kg of high‐purity oxide powders to provide reference materials for microanalytical work. These glasses have andesitic major compositions and are doped with fifty‐four trace elements in nearly identical abundance (500, 50, 5 µg g^?1) using oxide powders or element solutions, and are named ARM‐1, 2 and 3, respectively. We further document that sector‐field (SF) ICP‐MS (Element 2 or Element XR) is capable of sweeping seventy‐seven isotopes (from ⁷Li to ²³⁸U, a total of sixty‐eight elements) in 1 s and, thus, is able to quantify up to sixty‐eight elements by laser sampling. Micro‐ and bulk analyses indicate that the glasses are homogeneous with respect to major and trace elements. This paper provides preliminary data for the ARM glasses using a variety of analytical techniques (EPMA, XRF, ICP‐OES, ICP‐MS, LA‐Q‐ICP‐MS and LA‐SF‐ICP‐MS) performed in ten laboratories. Discrepancies in the data of V, Cr, Ni and Tl exist, mainly caused by analytical limitations. Preliminary reference and information values for fifty‐six elements were calculated with uncertainties [2 relative standard error (RSE)] estimated in the range of 1–20%.     

Remediation of ground water containing chlorinated and brominated hydrocarbons, benzene and chromate by sequential treatment using ZVI and GAC

A laboratory experiment with two sequenced columns was performed as a preliminary study for the installation of a permeable reactive barrier (PRB) at a site where a mixed ground water contamination exists. The first column contained granular zero valent iron (ZVI), the second column was filled with granular activated carbon (GAC). Trichloromethane (TCM, 930 μg/l) and chlorobenzene (MCB, 260 μg/l) were added to the ground water from the site as the main contaminants. Smaller amounts (<60 μg/l) of benzene, 1,2-dichloroethane, 1,1,2-trichloroethane (1,1,2-TCA), 1,1-dichloroethene (1,1-DCE), trichloroethene (TCE), tetrachloroethene (PCE), 1,2-dichloropropane (1,2-DCP), bromodichloromethane (BDCM), dibromochloromethane (DBCM), tribromomethane (TBM), vinyl chloride and chromate were also added to the water to simulate the complex contamination pattern at the site of interest. PCE, TCE, 1,1-DCE, DBCM, BDCM, TBM, MCB and chromate were remediated in contact with ZVI, while the remaining contaminants showed incomplete degradation. A fraction of 8–16.5% TCM was converted to dichloromethane (DCM). Remaining contaminant concentrations were efficiently sorbed by the GAC until breakthrough of DCM was observed after 1,230 exchanged pore volumes in the GAC. The results show that the complex mixture of contaminants can be remediated by a sequenced PRB consisting of ZVI and GAC and that DCM sorption capacity is the critical parameter for the dimensions of the GAC reactor.     

Deposition of sulfur dioxide to building stones: the influence of the ambient concentration on the deposition velocity

We report on extensive deposition measurements of sulfur dioxide (SO₂) on three types of commonly used building stones (Obernkirchen sandstone, Sand sandstone, Ihrlerstein sandstone). The deposition velocities on the three materials were determined in a number of measuring campaigns at different sites with different levels of air pollution. The measurements clearly imply that there is a strong influence of SO₂ concentration on the deposition velocity. With increasing concentration there is a strong decrease in the deposition velocity. To understand this deposition behavior a simple model with a single rate constant as the only adjustable parameter was established. Rate constants for the three stone materials were determined by least squares analysis and good agreement between experimental and calculated deposition velocities was obtained. According to the model treatment the surface resistance of stone materials increases with increasing SO₂ concentration due to a decrease of the pH in surface films. It follows from the concentration dependence of the deposition velocity that emission control measures for the reduction of ambient SO₂ concentrations do not lead to a proportional reduction of the SO₂ deposition. At low SO₂ concentrations the differences in the deposition behavior of different stone materials diminish and stone surfaces behave like ideal absorbers under such conditions, i.e., the deposition velocity is controlled by the aerodynamic resistance.