Connecting Satellite Observations with Water Cycle Variables Through Land Data Assimilation: Examples Using the NASA GEOS-5 LDAS   总被引：1，自引：1，他引：0  

Rolf H. Reichle  Gabriëlle J. M. De Lannoy  Barton A. Forman  Clara S. Draper  Qing Liu 《Surveys in Geophysics》2014,35(3):577-606

A land data assimilation system (LDAS) can merge satellite observations (or retrievals) of land surface hydrological conditions, including soil moisture, snow, and terrestrial water storage (TWS), into a numerical model of land surface processes. In theory, the output from such a system is superior to estimates based on the observations or the model alone, thereby enhancing our ability to understand, monitor, and predict key elements of the terrestrial water cycle. In practice, however, satellite observations do not correspond directly to the water cycle variables of interest. The present paper addresses various aspects of this seeming mismatch using examples drawn from recent research with the ensemble-based NASA GEOS-5 LDAS. These aspects include (1) the assimilation of coarse-scale observations into higher-resolution land surface models, (2) the partitioning of satellite observations (such as TWS retrievals) into their constituent water cycle components, (3) the forward modeling of microwave brightness temperatures over land for radiance-based soil moisture and snow assimilation, and (4) the selection of the most relevant types of observations for the analysis of a specific water cycle variable that is not observed (such as root zone soil moisture). The solution to these challenges involves the careful construction of an observation operator that maps from the land surface model variables of interest to the space of the assimilated observations.  相似文献   

Border Tax adjustment – legal perspective     

Rolf H. Weber 《Climatic change》2015,133(3):407-417

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Modelling thermal transients from magmatic underplating—an example from the Vøring margin (NE Atlantic)     

Magnus Wangen  Rolf Mjelde  Jan Inge Faleide 《Computational Geosciences》2011,15(4):771-788

The thermal impact of several kilometre-thick magmatic underplating in the lower continental crust is studied with analytical and numerical methods. Simple analytical solutions are derived for the thermal transient in the case of an infinite depth below the underplate and also for the case of a finite depth (down to the asthenosphere). It is shown that these solutions lead to simple approximations for when the transient surface heat flow is at its maximum, what the maximum is, and for how long the transient lasts. Even though these solutions assume that the underplate is emplaced instantaneously, they are useful in the interpretation of underplating over finite time spans. A numerical scheme is suggested for the modelling of underplating that handles both short time intervals as well as long intervals. The scheme treats magmatic underplating in a mass and energy conservative manner, and it is compared against the analytical solutions. Finally, the analytical and numerical results for thermal transients are applied to a transect from the Vøring margin (NE Atlantic), with respect to various degrees of early Cenozoic magmatic intrusion. It appears that more than half of the lower crustal body (LCB) in the Vøring margin must be magmatic underplating for the vitrinite reflectance to be substantially higher than for the non-magmatic case, where the LCB is assumed to comprise Caledonian crust.  相似文献   

Calcite Dissolution Kinetics     

Rolf?S.?ArvidsonEmail author  Cornelius?Fischer  Andreas?Luttge 《Aquatic Geochemistry》2015,21(5):415-422

We compare the canonical treatment of calcite’s dissolution rate from the literature in a closed system, particle batch reactor, with the alternative approach suggested by Truesdale (Aquat Geochem, 2015). We show that the decay of rate over time can be understood in terms of the evolution and distribution of reactive sites on the surface of these particles. We also emphasize that interpretation of observed rates must not exclude the fundamental role of crystal defects, whose importance is already implicitly reflected in the common form of rate laws in geochemistry. The empirical behavior of overall rate in closed systems, such as those described by Truesdale, may thus reflect relationships between defect centers and the generation of steps over the calcite surface (previously documented for silicates), such that below a critical free energy limit, there is insufficient driving force to open hollow cores and thus a loss of reaction mechanism. Dissolution in this very-near-equilibrium regime will be dependent on the distribution of extant steps and the energetics of new kink site nucleation. However, these sensitivities are complicated in the case of particle systems by grain boundaries, edges, corners, and other terminations. Such discontinuities constitute a defect class whose overall kinetic importance will be strongly tied to particle diameter and which can act independently of the internal strain field imposed by screw and edge dislocations.  相似文献   

Uranium–lead ages of apatite from iron oxide ores of the Bafq District,East-Central Iran     

Heinz-Günter Stosch  Rolf L. Romer  Farahnaz Daliran  Dieter Rhede 《Mineralium Deposita》2011,46(1):9-21

Iron oxide–apatite (IOA) deposits, often referred to as Kiruna-type iron ore deposits, are known to have formed from the Proterozoic to the Tertiary. They are commonly associated with calc–alkaline volcanic rocks and regional- to deposit-scale metasomatic alteration. In the Bafq District in east Central Iran, economic iron oxide–apatite deposits occur within felsic volcanic tuffs and volcanosedimentary sequences of Early Cambrian age. In order to constrain the age of formation of these ores and their relationship with the Early Cambrian magmatic event, we have determined the U–Pb apatite age for five occurrences in the Bafq District. In a ²⁰⁶Pb/²³⁸U vs. ²⁰⁷Pb/²³⁵U diagram, apatite free of or poor in inclusions of other minerals plots along the Concordia between 539 and 527 Ma with four out of five samples from one deposit clustering at the upper end of this range. For this deposit, we interpret this cluster to represent the age of apatite formation, whereas the spread towards younger ages may reflect either minor Pb loss or several events of IOA formation. Apatite with inclusions of monazite (±xenotime) yields disturbed systems with inclusions having developed after formation of the iron ore–apatite deposits, possibly as late as 130–140 Ma ago. Obtained apatite ages confirms that (IOA) and the apatite-rich rocks (apatites) of the Bafq district formed coevally with the Early Cambrian magmatic (-metasomatic) events.  相似文献   

Hydro-geochemical processes in an area with saline groundwater in lower Shire River valley, Malawi: An integrated application of hierarchical cluster and principal component analyses   总被引：2，自引：0，他引：2  

Maurice Monjerezi  Rolf D. VogtPer Aagaard  John D.K. Saka 《Applied Geochemistry》2011,26(8):1399-1413

Our ability to adapt to changes in groundwater quality, arising from a changing climate and/or local pressures, is dependent on comprehension of the governing controls of spatial variation in groundwater chemistry. This paper presents results of an assessment of dominant hydro-geochemical processes controlling groundwater chemical composition, using an integrated application of hierarchical cluster analysis (HCA) and principal component analysis (PCA) of a major ion dataset of groundwater from lower Shire River valley, Malawi. The area is in the southernmost part of the western section of the East African Rift System (EARS) and has localised occurrence of saline groundwater. HCA classified samples into three main clusters (C1-C3) according to their dominant chemical composition: C1 (dominant composition: Na-Cl; median TDS: 3436 mg L⁻¹), C2 (dominant composition: Na-HCO₃; median TDS: 966 mg L⁻¹) and C3 (dominant composition: alkali earths-HCO₃; median TDS: 528 mg L⁻¹). These clusters were in turn described by the principal components PC1, PC3 and PC2, respectively, resulting from the PCA. The results of the PCA and geochemical interpretation suggest that the spatial variation of groundwater quality in the area is influenced by the following processes: C3 samples result mainly from H₂CO₃ weathering of aluminosilicate minerals by percolating water supersaturated with CO₂. In addition to aluminosilicate weathering, C2 samples are influenced by the processes of cation exchange of Ca²⁺ and Mg²⁺ in the water for Na⁺ on clay minerals, and carbonate precipitation. The increase in ionic strength of C2 samples is attributed to mixing with high TDS groundwater in proximity with C2 samples. The saline/brackish C1 groundwater results from the processes of evaporation (for samples with high water table close to the Shire marshes) and dissolution of Cl⁻ and SO₄-evaporative salts followed by mineralised seep from sedimentary Karoo and Cretaceous Lupata sandstones.  相似文献   

A comment on the article “A collinearity diagnosis of the GNSS geocenter determination” by P. Rebischung,Z. Altamimi,and T. Springer     

Michael Meindl  Gerhard Beutler  Daniela Thaller  Rolf Dach  Stefan Schaer  Adrian Jäggi 《Journal of Geodesy》2015,89(2):189-194

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Time variable Earth’s gravity field from SLR satellites   总被引：4，自引：4，他引：0  

Krzysztof Sośnica  Adrian Jäggi  Ulrich Meyer  Daniela Thaller  Gerhard Beutler  Daniel Arnold  Rolf Dach 《Journal of Geodesy》2015,89(10):945-960

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A consistent combination of GNSS and SLR with minimum constraints   总被引：1，自引：1，他引：0  

Susanne Glaser  Mathias Fritsche  Krzysztof Sośnica  Carlos Javier Rodríguez-Solano  Kan Wang  Rolf Dach  Urs Hugentobler  Markus Rothacher  Reinhard Dietrich 《Journal of Geodesy》2015,89(12):1165-1180

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Microbially influenced formation of Mg‐calcite and Ca‐dolomite in the presence of exopolymeric substances produced by sulphate‐reducing bacteria     

Tomaso R. R. Bontognali  Judith A. McKenzie  Rolf J. Warthmann  Crisogono Vasconcelos 《地学学报》2014,26(1):72-77

Some species of sulphate‐reducing bacteria (SRB) are known to mediate the formation of dolomite and Mg‐calcite. However, their exact role in the mineralization process remains elusive. Here, we present the result of a laboratory experiment that was designed to test whether formation of carbonate minerals by SRB can occur in the absence of living cells, through passive mineralization of their exopolymeric substances (EPS). SRB capable of mediating dolomite were cultivated in the laboratory, allowing them to secrete EPS. Microbial activity within the cultures was subsequently inhibited with antibiotics. Only after this step, Ca²⁺ and Mg²⁺ were added to the solution and carbonate minerals could form. Mg‐calcite and disordered Ca‐dolomite precipitated in association with EPS. The mol.% of Mg²⁺ in the crystals increased with longer incubation times. This result demonstrates that organic compounds produced by SRB can mediate the formation of Ca‐Mg carbonates in the absence of an active metabolism.  相似文献