Meteorology and oceanography of the Atlantic sector of the Southern Ocean—a review of German achievements from the last decade     

Hartmut H. Hellmer  Monika Rhein  Günther Heinemann  Janna Abalichin  Wafa Abouchami  Oliver Baars  Ulrich Cubasch  Klaus Dethloff  Lars Ebner  Eberhard Fahrbach  Martin Frank  Gereon Gollan  Richard J. Greatbatch  Jens Grieger  Vladimir M. Gryanik  Micha Gryschka  Judith Hauck  Mario Hoppema  Oliver Huhn  Torsten Kanzow  Boris P. Koch  Gert König-Langlo  Ulrike Langematz  Gregor C. Leckebusch  Christof Lüpkes  Stephan Paul  Annette Rinke  Bjoern Rost  Michiel Rutgers van der Loeff  Michael Schröder  Gunther Seckmeyer  Torben Stichel  Volker Strass  Ralph Timmermann  Scarlett Trimborn  Uwe Ulbrich  Celia Venchiarutti  Ulrike Wacker  Sascha Willmes  Dieter Wolf-Gladrow 《Ocean Dynamics》2016,66(11):1379-1413

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Quartz as indicator mineral in the Central Swiss Alps: the quartz recrystallization isograd in the rock series of the northern Aar massif     

Hans Ulrich Bambauer  Marco Herwegh  Herbert Kroll 《Swiss Journal of Geoscience》2009,102(2):345-351

Earlier observations on the deformation of rock-forming quartz during Alpine metamorphism that were made by Voll (1976) along a traverse following the Reuss valley (Aar massif, Central Swiss Alps) are still relevant but can be explained in more modern term. Voll found that a few kilometres south of the contact between the Aar massif and its sedimentary cover quartz has partly undergone a combination of dynamic recrystallization and nucleation along grain boundaries and fractures at the expense of the deformed parent grains. Further to the south, increasing grain growth of quartz under nearly static conditions is observed, with polygonal grain shapes typical of annealed microfabrics. Comparable stages of recrystallization could be found in several N–S traverses through the Aar massif so that “points of first occurrence” of newly formed quartz could be connected to define a quartz recrystallization isograd. This isograd extents over 90 km through the northern Aar massif, following a course parallel to the sanidine/microcline isograd but at a distance of 10–15 km further to the north. The evolution of the quartz microfabric is discussed with respect to recent estimates of the T-t path of the Aar massif.  相似文献   

Modelling forest snow processes with a new version of WaSiM     

Kristian Förster  Jakob Garvelmann  Gertraud Meißl  Ulrich Strasser 《水文科学杂志》2013,58(10):1540-1557

ABSTRACT

We present a new model extension for the Water balance Simulation Model, WaSiM, which features (i) snow interception and (ii) modified meteorological conditions under coniferous forest canopies, complementing recently developed model extensions for particular mountain hydrological processes. Two study areas in Austria and Germany are considered in this study. To supplement and constrain the modelling experiments with on-site observations, a network of terrestrial time-lapse cameras was set up in one of these catchments. The spatiotemporal patterns of snow depth inside the forest and at the adjacent open field sites were recorded along with snow interception dynamics. Comparison of observed and modelled snow cover and canopy interception indicates that the new version of WaSiM reliably reconstructs the variability of snow accumulation for both the forest and the open field. The Nash-Sutcliffe efficiency computed for selected runoff events in spring increases from ?0.68 to 0.71 and 0.21 to 0.87, respectively.  相似文献   

Shear velocity estimates in rough‐bed open‐channel flow     

Fereshteh Bagherimiyab  Ulrich Lemmin 《地球表面变化过程与地形》2013,38(14):1714-1724

Shear velocity u_* is an important parameter in geophysical flows, in particular with respect to sediment transport dynamics. In this study, we investigate the feasibility of applying five standard methods [the logarithmic mean velocity profile, the Reynolds stress profile, the turbulent kinetic energy (TKE) profile, the wall similarity and spectral methods] that were initially developed to estimate shear velocity in smooth bed flow to turbulent flow over a loose bed of coarse gravel (D₅₀ = 1·5 cm) under sub‐threshold conditions. The analysis is based on quasi‐instantaneous three‐dimensional (3D) full depth velocity profiles with high spatial and temporal resolution that were measured with an Acoustic Doppler Velocity Profiler (ADVP) in an open channel. The results of the analysis confirm the importance of detailed velocity profile measurements for the determination of shear velocity in rough‐bed flows. Results from all methods fall into a range of ± 20% variability and no systematic trend between methods was observed. Local and temporal variation in the loose bed roughness may contribute to the variability of the logarithmic profile method results. Estimates obtained from the TKE and Reynolds stress methods reasonably agree. Most results from the wall similarity method are within 10% of those obtained by the TKE and Reynolds stress methods. The spectral method was difficult to use since the spectral energy of the vertical velocity component strongly increased with distance from the bed in the inner layer. This made the choice of the reference level problematic. Mean shear stress for all experiments follows a quadratic relationship with the mean velocity in the flow. The wall similarity method appears to be a promising tool for estimating shear velocity under rough‐bed flow conditions and in field studies where other methods may be difficult to apply. This method allows for the determination of u_* from a single point measurement at one level in the intermediate range (0·3 < h < 0·6). Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

Catalyzed Reactions on Mineral Plaster Materials Used for Indoor Air Purification     

Jan Gunschera  Doreen Markewitz  Ulrich Koberski  Tunga Salthammer 《洁净——土壤、空气、水》2013,41(5):437-446

Zeolites have been used for a long time for purification and catalytical purposes. Recently, first products appeared on the market using zeolites also for improving the indoor air quality so far volatile organic compounds (VOC) are concerned. However, porous compounds like zeolites can be found also in plaster material. Therefore, it was manifest to evaluate the capability of plaster with regard to air cleaning. In this article, the contribution of plaster compounds toward adsorption and catalytical decomposition of VOCs is evaluated using α‐pinene, chlorobenzene, 2‐ethoxyethylacetate, and pentanal as target substances under standard conditions (23°C, 50% r.H.). These compounds were chosen because of their VOC typical physicochemical properties like molecular dimensions, density, boiling point, vapor pressure, and octanol–water distribution coefficient (logk_ow). Hydrated lime and metakaolin were found out to have good adsorption properties under these circumstances. Also natural zeolites showed good results especially on pentanal. By investigations in environmental chambers the reduction potential of test plasters on chlorobenzene and 2‐ethoxyethylacetate concentrations could be shown. Application of coatings had no or only temporary influence on the performance of the plaster. Additional tests in small chambers demonstrated the possibility to improve the properties of plasters with help of FAU‐ or MFI‐type zeolites but the experiments also showed that α‐pinene and pentanal undergo chemical reactions. Further effort should be made on investigations also toward other compounds, especially more volatile ones like formaldehyde. Also additional building materials like insulation material or boards should be taken into account.  相似文献   

Fluid inclusion study of the Wunugetu Cu–Mo deposit,Inner Mongolia,China     

Nuo?Li  Yan-Jing?ChenEmail author  Thomas?Ulrich  Yong?Lai 《Mineralium Deposita》2012,47(5):467-482

Hydrothermal alteration and mineralization at the Wunugetu porphyry Cu–Mo deposit, China, include four stages, i.e., the early stage characterized by quartz, K-feldspar and minor mineralization, followed by a molybdenum mineralization stage associated with potassic alteration, copper mineralization associated with sericitization, and the last Pb–Zn mineralization stage associated with carbonation. Hydrothermal quartz contains three types of fluid inclusions, namely aqueous (W-type), daughter mineral-bearing (S-type) and CO₂-rich (C-type) inclusion, with the latter two types absent in the late stage. Fluid inclusions in the early stage display homogenization temperatures above 510°C, with salinities up to 75.8 wt.% NaCl equivalent. The presence of S-type inclusions containing anhydrite and hematite daughter minerals and C-type inclusions indicates an oxidizing, CO₂-bearing environment. Fluid inclusions in the Mo- and Cu-mineralization stages yield homogenization temperatures of 342–508°C and 241–336°C, and salinities of 8.6–49.4 and 6.3–35.7 wt.% NaCl equivalent, respectively. The presence of chalcopyrite instead of hematite and anhydrite daughter minerals in S-type inclusions indicates a decreasing of oxygen fugacity. In the late stage, fluid inclusions yield homogenization temperatures of 115–234°C and salinities lower than 12.4 wt.% NaCl equivalent. It is concluded that the early stage fluids were CO₂ bearing, magmatic in origin, and characterized by high temperature, high salinity, and high oxygen fugacity. Phase separation occurred during the Mo- and Cu-mineralization stages, resulting in CO₂ release, oxygen fugacity decrease and rapid precipitation of sulfides. The late-stage fluids were meteoric in origin and characterized by low temperature, low salinity, and CO₂ poor.  相似文献   

Geochemical Stratigraphy and Microvertebrate Assemblage Sequences across the Silurian/Devonian Transition in South China     

ZHAO Wenjin  WANG Nianzhong  ZHU Min  Ulrich MANN  Ulrich HERTEN  Andreas LüCKE 《《地质学报》英文版》2011,85(2):340-353

Carbon isotope (δ13Corg) analyses of non-marine clastic rocks and neritic carbonates and black shales spanning the Silurian/Devonian transition are compared from two richly fossiliferous sequences in Qujing of East Yunnan and Zoige of Sichuan, South China. The two sections, Xishancun and Putonggou sections in South China, reveal positive δ13Corg shifts happening in the Upper Pridoli and Lower Devonian and reaching peak values as heavy as ?25.2‰ (Xishancun) and ?19.9‰ (Putonggou) in the lowermost Lochkovian following the first occurrence of the thelodont Parathelodus and the conodont Icriodus woschmidti woschmidti (only in Putonggou Section and together with Protathyris-Lanceomyonia brachiopod fauna). These results replicate a globally known positive shift in δ13Corg from the uppermost Silurian to the lowermost Devonian. The δ13Corg variations across the Silurian/Devonian Boundary (SDB) at the two sections in South China exhibit a shift in carbon isotopic composition similar to the detailed SDB curves from the borehole Klonk-1 drilled at top of the Klonk Global Standard Stratotype-Section and Point (GSSP) in the Prague Basin, Czech Republic. In addition, four microvertebrate assemblages, including the Liaojiaoshan, Xishancun, Yanglugou and Xiaputonggou assemblages, are recognized from the Silurian/Devonian transition exposed in the Xishancun and Putonggou sections, respectively. The results from both carbon isotope stratigraphy and microvertebrate assemblage sequences suggest that the SDB in South China is located at the base of the Xishancun Formation (between sample QX-20 and sample QX-21) in the Xishancun Section and the lower part of the Xiaputonggou Formation (between sample ZP-09 and sample ZP-10) in the Putonggou Section. The isotopic trend for organic carbon together with the changes of microvertebrate remains across the SDB can offer an approach to a potential correlation of the SDB from different sedimentary facies, which help to correlate the marine with non-marine deposits.  相似文献   

Stabilization of extracellular polymeric substances (Bacillus subtilis) by adsorption to and coprecipitation with Al forms     

Robert Mikutta  Ulrich Zang  Ludwig Haumaier 《Geochimica et cosmochimica acta》2011,75(11):3135-3154

Extracellular polymeric substances (EPS) are continuously produced by bacteria during their growth and metabolism. In soils, EPS are bound to cell surfaces, associated with biofilms, or released into solution where they can react with other solutes and soil particle surfaces. If such reaction results in a decrease in EPS bioaccessibility, it may contribute to stabilization of microbial-derived organic carbon (OC) in soil. Here we examined: (i) the chemical fractionation of EPS produced by a common Gram positive soil bacterial strain (Bacillus subtilis) during reaction with dissolved and colloidal Al species and (ii) the resulting stabilization against desorption and microbial decay by the respective coprecipitation (with dissolved Al) and adsorption (with Al(OH)_3(am)) processes. Coprecipitates and adsorption complexes obtained following EPS-Al reaction as a function of pH and ionic strength were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The stability of adsorbed and coprecipitated EPS against biodegradation was assessed by mineralization experiments for 1100 h. Up to 60% of the initial 100 mg/L EPS-C was adsorbed at the highest initial molar Al:C ratio (1.86), but this still resulted only in a moderate OC mass fraction in the solid phase (17 mg/g Al(OH)_3(am)). In contrast, while coprecipitation by Al was less efficient in removing EPS from solution (maximum values of 33% at molar Al:C ratios of 0.1-0.2), the OC mass fraction in the solid product was substantially larger than that in adsorption complexes. Organic P compounds were preferentially bound during both adsorption and coprecipitation. Data are consistent with strong ligand exchange of EPS phosphoryl groups during adsorption to Al(OH)_3(am), whereas for coprecipitation weaker sorption mechanisms are also involved. X-ray photoelectron analyses indicate an intimate mixing of EPS with Al in the coprecipitates, which is not observed in the case of EPS adsorption complexes. The incubation experiments showed that both processes result in overall stabilization of EPS against microbial decay. Stabilization of adsorbed or coprecipitated EPS increased with increasing molar Al:C ratio and biodegradation was correlated with EPS desorption, implying that detachment of EPS from surface sites is a prerequisite for microbial utilization. Results indicate that the mechanisms transferring EPS into Al-organic associations may significantly affect the composition and stability of biomolecular C, N and P in soils. The observed efficient stabilization of EPS might explain the strong microbial character of organic matter in subsoils.  相似文献   

The significance of isotope specific diffusion coefficients for reaction-transport models of sulfate reduction in marine sediments     

Ulrich G. Wortmann  Boris M. Chernyavsky 《Geochimica et cosmochimica acta》2011,75(11):3046-3056

Modeling isotopic signatures in systems affected by diffusion, advection, and a reaction which modifies the isotopic abundance of a given species, is a discipline in its infancy. Traditionally, much emphasis has been placed on kinetic isotope effects during biochemical reactions, while isotope effects caused by isotope specific diffusion coefficients have been neglected. A recent study by Donahue et al. (2008) suggested that transport related isotope effects may be of similar magnitude as microbially mediated isotope effects. Although it was later shown that the assumed differences in the isotope specific diffusion coefficients were probably overstated by one or two orders of magnitude (Bourg, 2008), this study raises several important issues: (1) Is it possible to directly calculate isotopic enrichment factors from measured concentration data without modeling the respective system? (2) Do changes in porosity and advection velocity modulate the influence of isotope specific diffusion coefficients on the fractionation factor α? (3) If one has no a priori knowledge whether diffusion coefficients are isotope specific or not, what is the nature and magnitude of the error introduced by either assumption? Here we argue (A) That the direct substitution of measured data into a differential equation is problematic and cannot be used as a replacement for a reaction-transport model; (B) That the transport related fractionation scales linearly with the difference between the respective diffusion coefficients of a given isotope system, but depends in a complex non-linear way on the interplay between advection velocity, and downcore changes of temperature and porosity. Last but not least, we argue that the influence of isotope specific diffusion coefficients on microbially mediated sulfate reduction in typical marine sediments is considerably smaller than the error associated with the determination of the fractionation factor.  相似文献   

Uranium speciation and stability after reductive immobilization in aquifer sediments     

Jonathan O. Sharp  Juan S. Lezama-Pacheco  Pilar Junier  Kai-Uwe Ulrich  Satya Chinni  Camille Margot-Roquier  Bradley M. Tebo  John R. Bargar 《Geochimica et cosmochimica acta》2011,75(21):6497-6510

It has generally been assumed that the bioreduction of hexavalent uranium in groundwater systems will result in the precipitation of immobile uraninite (UO₂). In order to explore the form and stability of uranium immobilized under these conditions, we introduced lactate (15 mM for 3 months) into flow-through columns containing sediments derived from a former uranium-processing site at Old Rifle, CO. This resulted in metal-reducing conditions as evidenced by concurrent uranium uptake and iron release. Despite initial augmentation with Shewanella oneidensis, bacteria belonging to the phylum Firmicutes dominated the biostimulated columns. The immobilization of uranium (∼1 mmol U per kg sediment) enabled analysis by X-ray absorption spectroscopy (XAS). Tetravalent uranium associated with these sediments did not have spectroscopic signatures representative of U-U shells or crystalline UO₂. Analysis by microfocused XAS revealed concentrated micrometer regions of solid U(IV) that had spectroscopic signatures consistent with bulk analyses and a poor proximal correlation (μm scale resolution) between U and Fe. A plausible explanation, supported by biogeochemical conditions and spectral interpretations, is uranium association with phosphoryl moieties found in biomass; hence implicating direct enzymatic uranium reduction. After the immobilization phase, two months of in situ exposure to oxic influent did not result in substantial uranium remobilization. Ex situ flow-through experiments demonstrated more rapid uranium mobilization than observed in column oxidation studies and indicated that sediment-associated U(IV) is more mobile than biogenic UO₂. This work suggests that in situ uranium bioimmobilization studies and subsurface modeling parameters should be expanded to account for non-uraninite U(IV) species associated with biomass.  相似文献