Modification of fluid inclusions in quartz by deviatoric stress. II: experimentally induced changes in inclusion volume and composition     

Larryn W. Diamond  Alexandre Tarantola  Holger Stünitz 《Contributions to Mineralogy and Petrology》2010,160(6):845-864

Fluid inclusions in quartz are known to modify their densities during shear deformation. Modifications of chemical composition are also suspected. However, such changes have not been experimentally demonstrated, their mechanisms remain unexplained, and no criteria are available to assess whether deformed inclusions preserve information on paleofluid properties. To address these issues, quartz crystals containing natural CO₂–H₂O–NaCl fluid inclusions have been experimentally subjected to compressive deviatoric stresses of 90–250 MPa at 700°C and ~600 MPa confining pressure. The resulting microcracking of the inclusions leads to expansion by up to 20%, producing low fluid densities that bear no relation to physical conditions outside the sample. Nevertheless, the chemical composition of the precursor inclusions is preserved. With time the microcracks heal and form swarms of tiny satellite inclusions with a wide range of densities, the highest reflecting the value of the maximum principle stress, σ ₁. These new inclusions lose H₂O via diffusion, thereby passively increasing their salt and gas contents, and triggering plastic deformation of the surrounding quartz via H₂O-weakening. Using microstructural criteria to identify the characteristic types of modified inclusions, both the pre-deformation fluid composition and syn-deformation maximum stress on the host mineral can be derived from microthermometric analysis and thermodynamic modelling.  相似文献   

Bayesian updating via bootstrap filtering combined with data-driven polynomial chaos expansions: methodology and application to history matching for carbon dioxide storage in geological formations     

Sergey Oladyshkin  Holger Class  Wolfgang Nowak 《Computational Geosciences》2013,17(4):671-687

Model calibration and history matching are important techniques to adapt simulation tools to real-world systems. When prediction uncertainty needs to be quantified, one has to use the respective statistical counterparts, e.g., Bayesian updating of model parameters and data assimilation. For complex and large-scale systems, however, even single forward deterministic simulations may require parallel high-performance computing. This often makes accurate brute-force and nonlinear statistical approaches infeasible. We propose an advanced framework for parameter inference or history matching based on the arbitrary polynomial chaos expansion (aPC) and strict Bayesian principles. Our framework consists of two main steps. In step 1, the original model is projected onto a mathematically optimal response surface via the aPC technique. The resulting response surface can be viewed as a reduced (surrogate) model. It captures the model’s dependence on all parameters relevant for history matching at high-order accuracy. Step 2 consists of matching the reduced model from step 1 to observation data via bootstrap filtering. Bootstrap filtering is a fully nonlinear and Bayesian statistical approach to the inverse problem in history matching. It allows to quantify post-calibration parameter and prediction uncertainty and is more accurate than ensemble Kalman filtering or linearized methods. Through this combination, we obtain a statistical method for history matching that is accurate, yet has a computational speed that is more than sufficient to be developed towards real-time application. We motivate and demonstrate our method on the problem of CO₂ storage in geological formations, using a low-parametric homogeneous 3D benchmark problem. In a synthetic case study, we update the parameters of a CO₂/brine multiphase model on monitored pressure data during CO₂ injection.  相似文献   

Mobilisation and transport of dissolved organic carbon and iron in peat catchments—Insights from the Lehstenbach stream in Germany using generalised additive models     

Benny Selle  Klaus‐Holger Knorr  Gunnar Lischeid 《水文研究》2019,33(25):3213-3225

During the last decades, increasing exports of both dissolved organic carbon (DOC) and iron were observed from peat catchments in North America and Europe with potential consequences for water quality of streamwater and carbon storages of soils. As mobilisation and transport processes of DOC and iron in peat catchments are only partly understood, the purpose of this study was to elucidate these processes in an intensively monitored and studied system. Specifically, it was hypothesised that dissimilatory iron reduction in riparian peatland soils mobilises DOC initially adsorbed to iron minerals. During stormflow conditions, both DOC and iron will be transported into the stream network. Ferrous iron may be reoxidised at redox interfaces on its way to the stream, and subsequently, ferric iron could be transported together with DOC as complexes. To test these hypotheses, generalised additive models (GAMs) were applied to 14 years of weekly time series of discharge and concentrations of selected solutes measured in a German headwater stream called Lehstenbach. This stream drains a 4.19‐km² forested mountain catchment; one third of which is covered by riparian peatland soils. We interpreted results of different types of GAM in the way that (a) iron reduction drove the mobilisation of DOC from peatland soils and that (b) both iron and DOC were transported as complexes after their joint mobilisation to and within the steam. It was speculated that low nitrate availability in the uppermost wetland soil layer, particularly during the growing season, promoted iron reduction and thus the mobilisation of DOC. However, the influence of nitrate on the DOC mobilisation remains relatively uncertain. This influence could be further investigated using methods similar to the GAM analysis conducted here for other catchments with long‐term data as well as detailed measurements of the relevant species in riparian wetland soils and the adjacent stream network.  相似文献   

Determination of groundwater discharge rates and water residence time of groundwater‐fed lakes by stable isotopes of water (18O, 2H) and radon (222Rn) mass balances          下载免费PDF全文

Eric Petermann  John J. Gibson  Kay Knöller  Thomas Pannier  Holger Weiß  Michael Schubert 《水文研究》2018,32(6):805-816

Lacustrine groundwater discharge (LGD) and the related water residence time are crucial parameters for quantifying lake matter budgets and assessing its vulnerability to contaminant input. Our approach utilizes the stable isotopes of water (δ¹⁸O, δ²H) and the radioisotope radon (²²²Rn) for determining long‐term average and short‐term snapshots in LGD. We conducted isotope balances for the 0.5‐km² Lake Ammelshainer See (Germany) based on measurements of lake isotope inventories and groundwater composition accompanied by good quality and comprehensive long‐term meteorological and isotopic data (precipitation) from nearby monitoring stations. The results from the steady‐state annual isotope balances that rely on only two sampling campaigns are consistent for both δ¹⁸O and δ²H and suggested an overall long‐term average LGD rate that was used to infer the water residence time of the lake. These findings were supported by the good agreement of the simulated LGD‐driven annual cycles of δ¹⁸O and δ²H lake inventories with the observed lake isotope inventories. However, radon mass balances revealed lower values that might be the result of seasonal LGD variability. For obtaining further insights into possible seasonal variability of groundwater–lake interaction, stable water isotope and radon mass balances could be conducted more frequently (e.g., monthly) in order to use the derived groundwater discharge rates as input for time‐variant isotope balances.  相似文献   

Validation of Aura Microwave Limb Sounder water vapor and ozone profiles over the Tibetan Plateau and its adjacent region during boreal summer     

YAN XiaoLu  ZHENG XiangDong  ZHOU XiuJi  Holger VMEL  SONG JianYang  LI Wei  MA YongHong  ZHANG Yong 《中国科学:地球科学(英文版)》2015,58(4):589-603

We present validation studies of MLS V2.2 and V3.3 water vapor(WV) and ozone profiles over the Tibetan Plateau(Naqu and Lhasa) and its adjacent region(Tengchong) respectively by using the balloon-borne Cryogenic Frost point Hygrometer and Electrochemical Concentration Cell ozonesonde. Coincident in situ measurements were selected to compare the MLS V2.2 and V3.3 WV and ozone profiles for understanding the applicability of the two version MLS products over the region. MLS V2.2 and V3.3 WV profiles respectively show their differences within ?2.2±15.7%(n=74) and 0.3±14.9%(n=75) in the stratosphere at and above 82.5 h Pa. Accordingly, at 100 h Pa, the altitude approaching the tropopuase height, differences are within 9.8± 46.0%(n=18) and 23.0±45.8%(n=17), and they are within 21.5±90.6%(n=104) and 6.0±83.4%(n=99) in upper troposphere. The differences of MLS ozone are within ?11.7±16.3%(n=135, V2.2) and 15.6±24.2%(n=305, V3.3) at and above 82.5 h Pa. At 100 h Pa, they are within ?3.5±54.4%(n=27) and ?8.7±41.6%(n=38), and within 18.0±79.1%(n=47) and 34.2±76.6%(n=160) in the upper troposphere. The relative difference of MLS WV and ozone profile has significant oscillation and scatter at upper troposphere and lower stratosphere partly due to the stronger gradients of WV and ozone concentrations here as well the linear interpolation of sonde data for the intercomparison. At and below 70 h Pa, the relative differences of MLS ozone are significantly larger over Lhasa during the Tibetan Plateau "ozone valley" season, which is also the Asian Summer Monsoon period. The MLS ozone differences over the three sites are similar in their vertical distributions during that period. A simple linear correlation analysis between MLS and sonde profiles indicates that the sensitivity of MLS profile products is related to concentrations at each pressure level. The MLS V3.3 product sensitivity is slightly improved for WV at and above 82.5 h Pa, whereas it is not obvious for ozone. The possible factors contributing to the differences of the MLS profile products of WV and ozone are discussed.  相似文献   

Mercury isotope fractionation during photoreduction in natural water is controlled by its Hg/DOC ratio   总被引：2，自引：0，他引：2  

Wang Zheng  Holger Hintelmann 《Geochimica et cosmochimica acta》2009,73(22):6704-390

Photoreduction of Hg in natural water plays a crucial role in the production of elemental Hg and its biogeochemical cycle. Solar irradiation and dissolved organic carbon (DOC) in water are considered to be the major factors inducing Hg photoreduction. We investigated Hg isotope fractionation during photoreduction and its relationship with Hg/DOC ratios. Both mass dependent (MDF) and mass independent fractionation (MIF) was observed. MIF enriched ¹⁹⁹Hg and ²⁰¹Hg in the reactant Hg(II) and thus, significantly enhanced the fractionation between odd and even isotopes. This direction of MIF is consistent with magnetic isotope effect as the underlying cause for the odd isotope enrichment in reactants. MIF also occurred in dark controls. But in the absence of light, ¹⁹⁹Hg and ²⁰¹Hg were enriched in the product Hg(0), which is not explained by magnetic isotope effects. We propose that nuclear volume effect dominated Hg isotope fractionation under these conditions. The reduction kinetics and isotope fractionation during photoreduction strongly correlated to Hg/DOC concentration ratios. Although different reduction kinetics and fractionation factors were measured at different Hg/DOC ratios, the same Hg/DOC ratios led to almost identical results. The degree of MIF for the two odd isotopes was also affected by Hg/DOC ratios. For this reason, it is critical to study Hg photoreduction at a near-natural Hg/DOC ratio in order to better simulate natural conditions. We suggest that differences in Hg-DOC binding, which varies with Hg/DOC ratios, may be responsible for the relationship between Hg/DOC ratios and Hg photoreduction.  相似文献   

Preface     

Holger Class  Helge Dahle  Rainer Helmig 《Computational Geosciences》2009,13(4):405-407

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Meteorological influence on upwelling off Northwest Africa     

Prof. Dr. Peter Speth  Dipl-Math. Holger Detlefsen  Dipl.-Met. Hans-Werner Sierts 《Ocean Dynamics》1978,31(3):95-104

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Late Pleistocene and Holocene history of Lake Terrasovoje,Amery Oasis,East Antarctica,and its climatic and environmental implications   总被引：1，自引：3，他引：1  

Bernd Wagner  Holger Cremer  Nadja Hultzsch  Damian B. Gore  Martin Melles 《Journal of Paleolimnology》2004,32(4):321-339

A 5.52 m long sediment sequence was recovered from Lake Terrasovoje, Amery Oasis, East Antarctica, in order to reconstruct the regional environmental history. The basal sediments, which are dominated by glacial and glaciofluvial clastic sediments, attest to a Late Pleistocene deglaciation of the lake basin. These sediments are overlain by 2.70 m of laminated algal and microbial mats and a few interspersed moss layers. Radiocarbon dating, conducted on bulk organic carbon of 12 samples throughout the organic sequence, provides a reliable chronology since the onset of biogenic accumulation at c. 12,400 cal. year BP. Successful diatom colonization, however, was probably hampered by extensive ice and snow cover on the lake and restricted input of nutrients until 10,200 cal. year BP. A subsequent increase of nutrient supply culminated between 8600 and 8200 cal. year BP and is related to warm summer temperatures and reduced albedo in the catchment. Warm conditions lasted until 6700 cal. year BP, supporting the establishment of a diatom community. Colder temperatures from 6700 cal. year BP culminated in several periods between 6200 and 3700 cal. year BP, when high amounts of sulphur and low abundances of diatoms were deposited due to a perennial ice and snow cover on the lake. During the late Holocene, relatively warm conditions between 3200 and 2300 cal. year BP and between 1500 to 1000 cal. year BP, respectively, indicated by high accumulation of organic matter and reducing bottom water conditions, were interrupted and followed by colder periods.  相似文献   

Weakening and strain localization produced by syn-deformational reaction of plagioclase   总被引：2，自引：0，他引：2  

Holger Stünitz  Jan Tullis 《International Journal of Earth Sciences》2001,90(1):136-148

There are many observations in naturally deformed rocks on the effects of mineral reactions on deformation, but few experimental data. In order to study the effects of chemical disequilibrium on deformation we have investigated the hydration reaction plagioclase + H₂OM more albitic plagioclase + zoisite + kyanite + quartz. We utilized fine-grained (2-6 µm) plagioclase aggregates of two compositions (An54 and An60), both dried and with 0.1-0.4 wt% H₂O present, in shear deformation experiments at two sets of conditions: 900 °C, 1.0 GPa (in the plagioclase stability field) and 750 °C, 1.5 GPa (in the zoisite stability field). Dry samples and those deformed in the plagioclase stability field underwent homogeneous shearing by dislocation creep, but samples with 0.1 to 0.4 wt% water deformed in the zoisite stability field showed extreme strain localization into very narrow (~1-3 µm) shear bands after low shear strain. In these samples the microstructures of reaction products in the matrix differ from those in the shear bands. In the matrix, large (up to 400 µm) zoisite crystals grew in the direction of finite extension, and relict plagioclase grains are surrounded by rims of recrystallized grains that are more albitic. In the shear bands, the reaction products albitic plagioclase, zoisite, white mica, and traces of kyanite form polyphase aggregates of very fine-grained (<0.1 µm) dislocation-free grains. Most of the sample strain after % ~2 has occurred within the shear bands, within which the dominant deformation mechanism is inferred to be diffusion-accommodated grain boundary sliding (DAGBS). The switch from dislocation creep in dry samples deformed without reaction to DAGBS in reacted samples is associated with a decrease in flow stress from ~800 to <200 MPa. These experiments demonstrate that heterogeneous nucleation driven in part by chemical disequilibrium can produce an extremely fine-grained polyphase assemblage, leading to a switch in deformation mechanism and significant weakening. Thus, localization of deformation in polyphase rocks may occur on any pressure (P),temperature (T)-path where the equilibrium composition of the constituent minerals changes.  相似文献