Multi-species chemical data assimilation with the Danish Eulerian hemispheric model: system description and verification     

Jeremy D. Silver  Jesper H. Christensen  Michael Kahnert  Lennart Robertson  Peter J. Rayner  Jørgen Brandt 《Journal of Atmospheric Chemistry》2016,73(3):261-302

Satellite retrievals of atmospheric composition provide a wealth of data on a global scale. These complement results from atmospheric chemistry-transport models (CTMs), and can be combined using data assimilation. We present two assimilation schemes coupled to the Danish Eulerian Hemispheric Model (DEHM), a three-dimensional, off-line CTM with full photochemistry: a variant on the ensemble Kalman filter and the three-dimensional variational scheme. The aim of this paper is to describe the two schemes and present an initial assessment of their impacts on model skill. Retrievals of multiple atmospheric trace gases are assimilated, namely: NO₂ tropospheric column densities, CH₄ total column densities, and partial column concentrations of O₃, CO and CH₄; these data are retrieved from four satellite sensors. Data for each species are assimilated independently of one another, and other species are only adjusted indirectly via the model’s chemistry and dynamics. Assimilation results are compared with measurements from surface monitoring stations and other satellite retrievals, and preliminary validation results are presented.Reference simulations (without assimilation) grossly underestimate surface CO concentrations, and both assimilation schemes eliminate this large and systematic model bias. The assimilation improves the spatial correlation of modelled CO with surface observations, and improves the spatial correlation between forecasts and retrievals for CO, NO₂ and O₃. Results for CH₄ show a loss of skill due to a mismatch in model bias between two assimilated CH₄ data-sets. Finally, we discuss differences in methodology and results between this paper and a recent study on multi-species chemical data assimilation. Joint optimisation of initial conditions and emission rates offers a promising direction for improving modelled boundary-layer concentrations.  相似文献   

Desertification in Africa — A critique and an alternative approach     

Lennart Olsson 《GeoJournal》1993,31(1):23-31

This article critically reviews the international debate on desertification, its status and rate as well as causes and consequences. The article rejects the commonly used concept of a degrading environment, but tries to explain the environmental problems as symptoms of a wider economic and political crisis. An alternative approach applying systems analysis of the entire socio-economic-system to the study of desertification and land degradation is discussed, with examples from the Western Sudan.  相似文献   

Spatial uniformity of sediment accumulation in varved lake sediments in northern Sweden     

G. Petterson  I. Renberg  P. Geladi  A. Lindberg  F. Lindgren 《Journal of Paleolimnology》1993,9(3):195-208

As part of an investigation aimed at assessing the potential of northern Swedish varved lake sediments for fine-resolution reconstruction of past climatic conditions, the following questions were addressed; how representative is a single core, does the appearance of varves change as the sediment ages, and how can varve thickness and within-varve structures be digitized? Analyses of replicate cores from Kassjön, using sample sequences of seasonal, annual and centennial time resolution, show that spatial variability of sediment accumulation in the varved sediment is very low. Comparisons of intensity curves from image analysis of freeze cores of recent sediments from Lake Nylandssjön, sampled in 1980 and 1985, indicate that the varves acquire their appearance at the sediment-water interface during sedimentation and that the varve structures are preserved during diagenetic processes. Measurement of varve thicknesses with a tree-ring microscope and with image analysis gave similar results. However, with image analysis, within-varve structures such as colour variations and thicknesses of seasonal layers, can also be recorded, increasing the possibilities for palaeolimnological and palaeoclimatic inferences.  相似文献   

Magma mixing,the petrogenetic link between anorthositic suites and rapakivi granites, Åland,SW Finland     

O. Eklund  S. Fröjdö  B. Lindberg 《Mineralogy and Petrology》1994,50(1-3):3-19

Summary The Åland, rapakivi batholith consists of several granites that differ texturally and mineralogically from quartz-porphyritic varieties to rapakivi varieties with K-feldspar ovoids (wiborgites and pyterlites) and aplitic granites. Closely associated with the batholith there is a mafc magmatic series of dolerite dykes, norites, anorthosites and monzodiorites.The earliest major intrusive phase of the Åland, rapakivi batholith consists of quartzporphyritic hornblende rapakivi. This rock contains small amoeboidal mafc enclaves, labradorite megacrysts, quartz ocelli, amphibole-mantled xenoliths and irregular clots of granophyric granite. These disequilibrium features are products of mixing between basaltic and granitic magmas. Geochemical modelling indicates that the quartzporphyritic hornblende rapakivi is a mixture of 15% hi-Fe monzodiorite (mafic endmember) and 85% quartz-feldspar porphyry (felsic end-member). The monzodiorite is derived from a norite-anorthosite-monzodiorite series. The quartz-feldspar porphyry is produced by partial melting of the country rock caused by intrusions of hot basic magma.Structural, textural and geochemical features suggest that magma mixing was an important petrogenetic process in the formation of the earliest rapakivi granite intrusions in the Åland, rapakivi batholith. Petrographic evidence of magma mixing can also be found in the major intrusion of the batholith, the wiborgite rapakivi granites. Chemically the mixing is difficult to specify in these rocks because of a high proportion of felsic component. Zircon and apatite fractionation trends, however, indicate that the wiborgite rapakivis also contain components from a mixed source.

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Magmamixing, die petrogenetische Verbindung zwischen Anorthositen und RapakiviGraniten, Åland, SW Finnland

Zusammenfassung Der Rapakivi Batholit von Åland besteht aus verschiedenen Graniten, die in ihrer Textur und Zusammensetzung das Feld von quarzporphyritischen über Rapakivigranite mit K-Feldspat-Ovoiden (Wiborgite und Pyterlite) und aplitischen Graniten abdecken. Eine mafische magmatische Serie von Dolerit-Gängen, Noriten, Anorthositen und Monzodioriten ist mit diesen Batholiten eng verbunden.Die erste größere Intrusivphase des Åland, Rapakivi Batholiten besteht aus quarzporphyritischem Hornblende Rapakivi. Dieses Gestein enhält kleine Amöboide, mafische Enklaven, Labradorit Megakristalle, Quarzocelli, Xenolithe mit Amphibolrändern und unregelmäßige Aggregate von granophyrischem Granit. Diese Produkte von Ungleichgewichts-Bedingungen gehen auf die Mischung zwischen basaltischen und granitischen Magmen zurück. Geochemische Modelle zeigen, daß der quarzporphyritische Hornblende-Rapakivi eine Mischung von 15%. eisenreichen Monzodiorit (mafisches Endglied) und 85% Quarz-Feldspatporphyr (felsisches Endglied) ist. Der Monzodiorit stammt von einer Norit-Anorthosit-Monzodiorit Serie. Der QuarzFeldspat-Porphyr entstand durch teilweise Aufschmelzung des Nebengesteines, die durch Intrusionen heißen basischen Magmas verursacht wurden.Strukturelle, texturelle und geochemische Daten zeigen, daß Magmamischung ein wichtiger petrogenetischer Prozeß der Bildung der frühesten Rapakivi-Granit-Intrusionen im Åland, Batholith waren. Petrographische Hinweise auf Magmamischung können auch in der größten Intrusion des Batholiths, dem Wiborg Rapakivi Granit, gefunden werden. Wegen des hohen Anteils felsischer Komponenten ist es schwierig, das Magmamixing in diesen Gesteinen chemisch zu quantifizieren. Zirkon- und Apatitfraktionierungs-Trends weisen jedoch darauf hin, daß auch die WiborgitRapakivis Komponenten aus einer gemischten Quelle enthalten.

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With 5 figures  相似文献   

Water flow and swelling pressure in non-saturated bentonite-based clay barriers     

Lennart Brgesson 《Engineering Geology》1985,21(3-4):229-237

The water uptake of 10 and 20% bentonite—sand mixtures and of 100% pure bentonite was studied experimentally. The results were compared with calculated water content distributions to study the usefulness of the diffusion equation. The relation between the swelling pressure and the degree of saturation of a bentonite was also studied.  相似文献   

Experimental evidence for an ascending microflow of geogas in the ground   总被引：2，自引：0，他引：2  

Lennart Malmqvist  Krister Kristiansson 《Earth and Planetary Science Letters》1984,70(2):407-416

A microflow of free ascending gas has been observed in 26 out of 30 tested boreholes at three different sites. The flow rates vary between 60 × 10⁻⁴ and 4 cm³/min m² horizontally projected borehole area. Sampling has been made in ground boreholes as well as in holes drilled downwards from the lowest levels in two mines. The composition of the gas varies considerably. The main components of the gas are nitrogen, argon, oxygen and methane. Traces of heavier hydrocarbons are observed. At the site of the ground holes, only traces of methane are observed. In all sampled holes the existence of free oxygen is observed. The nitrogen/argon quotient is close to the atmospheric quotient in all sampled holes, indicating a partly atmospheric origin of the gas. The existence of methane and traces of heavier hydrocarbons indicates the existence of a second source.  相似文献   

Temperature dependence of calcite dissolution kinetics between 1 and 62°C at pH 2.7 to 8.4 in aqueous solutions   总被引：1，自引：0，他引：1  

E.Lennart Sjöberg  David T. Rickard 《Geochimica et cosmochimica acta》1984,48(3):485-493

The kinetics of calcite dissolution in aqueous KCl-solutions far from equilibrium, between 1 and 62°C in the pH-range 2.7 to 8.4 have been investigated using a rotating disc apparatus. At neutral and alkaline pH in the mixed kinetic regime the empirical apparent activation energy (EAAE) for the surface chemical reaction rate constant is 54 ± 4 kJ mole^?1 for Carrara marble and 46 ± 4 kJ mole^?1 for Iceland spar. Under similar conditions the EAAE of the transport rate constant increases with decreasing temperature, but has a mean value of 27 ± 2 kJ mole^?1. The corresponding diffusion coefficient has a mean EAAE of 37 ± 3 kJ mole^?1 and this high EAAE is consistent with transport dependence on product diffusion in this H⁺-independent regime.In contrast, in acid solutions, where the rate approaches end-member transport control, the EAAE of the diffusion coefficient is 16 kJ mole^?1, also decreasing with increasing temperature. This is compatible with H⁺-diffusion to the surface being rate-controlling.In inhibitor-free natural systems, calcite dissolution kinetics far from equilibrium can be described in terms of three regimes: an H⁺-dependent regime (pH < 4 at 25°C), a transition regime (4 < pH < 5.5 at 25°C) and an H⁺-independent regime (pH > 5.5 at 25°C). At lower temperatures these boundaries move to higher pH values. The presence of inhibitors in natural systems may enhance surface controlled kinetics.  相似文献   

Analysis of I in groundwater samples: Direct and quantitative results below the drinking water standard     

Christopher F. Brown  Keith N. GeiszlerMichael J. Lindberg 《Applied Geochemistry》2007

This paper highlights an analytical method based on mass measurement that can be used to directly quantify ¹²⁹I in groundwater samples at concentrations below the maximum contaminant level (MCL) without the need for sample pre-concentration or extraction. Samples were analyzed on a Perkin Elmer ELAN DRC II ICP-MS after minimal dilution using O₂ as the reaction gas. Analysis of continuing calibration verification standards indicated that the dynamic reaction cell (DRC) mode could be used for quantitative analysis of ¹²⁹I in samples below the MCL (0.0057 ng/mL or 1 pCi/L). The low analytical detection limit of ¹²⁹I analysis in the DRC mode coupled with minimal sample dilution (1.02x) resulted in a final estimated quantification limit of 0.0051 ng/mL. Subsequent analysis of three groundwater samples containing ¹²⁹I resulted in fully quantitative results in the DRC mode, and spike recovery analyses performed on all three samples confirmed that the groundwater matrix did not adversely impact the analysis of ¹²⁹I in the DRC mode. This analytical approach has been proven to be a cost-effective, high-throughput technique for the direct, quantitative analysis of ¹²⁹I in groundwater samples at environmentally relevant concentrations that reach below the current MCL.  相似文献   

Strain parameters of discontinuities in rock for finite element calculation   总被引：1，自引：0，他引：1  

Roland Pusch  Lennart Brgesson 《Engineering Geology》1998,49(3-4):201-206

The bulk strain induced by excavation of rooms for storage of highly radioactive waste is usually unimportant, but the change in aperture and shear displacement of permeable fractures may be of practical importance. Hence, the normal and shear of such discontinuities have to be considered and are commonly predicted by using special deformation moduli termed “normal” and “shear” stiffnesses in numerical calculations. For the use of some finite element methods, these have to be converted to compression and shear moduli ,which, in turn, requires that the thickness of the discontinuity is known. The normal and shear strain can be expressed in terms of soil mechanical parameters, yielding the compression modulus M and the shear modulus G, with the required form for finite element calculations. By definition they are functions of the normal and shear stiffness K_n and K_s. It is concluded that calculation of the normal and shear strain of discontinuities with clastic fillings by the use of finite element methods and deformation moduli derived from stiffness numbers is very uncertain except when the geometry of the weaknesses can be accurately defined.  相似文献   

Hanford tank residual waste – Contaminant source terms and release models     

William J. Deutsch  Kirk J. Cantrell  Kenneth M. Krupka  Michael L. Lindberg  R. Jeffery Serne 《Applied Geochemistry》2011,26(9-10):1681-1693

Residual waste is expected to be left in 177 underground storage tanks after closure at the US Department of Energy’s Hanford Site in Washington State, USA. In the long term, the residual wastes may represent a potential source of contamination to the subsurface environment. Residual materials that cannot be completely removed during the tank closure process are being studied to identify and characterize the solid phases and estimate the release of contaminants from these solids to water that might enter the closed tanks in the future. As of the end of 2009, residual waste from five tanks has been evaluated. Residual wastes from adjacent tanks C-202 and C-203 have high U concentrations of 24 and 59 wt.%, respectively, while residual wastes from nearby tanks C-103 and C-106 have low U concentrations of 0.4 and 0.03 wt.%, respectively. Aluminum concentrations are high (8.2–29.1 wt.%) in some tanks (C-103, C-106, and S-112) and relatively low (<1.5 wt.%) in other tanks (C-202 and C-203). Gibbsite is a common mineral in tanks with high Al concentrations, while non-crystalline U–Na–C–O–P ± H phases are common in the U-rich residual wastes from tanks C-202 and C-203. Iron oxides/hydroxides have been identified in all residual waste samples studied to date. Contaminant release from the residual wastes was studied by conducting batch leach tests using distilled deionized water, a Ca(OH)₂-saturated solution, or a CaCO₃-saturated water. Uranium release concentrations are highly dependent on waste and leachant compositions with dissolved U concentrations one or two orders of magnitude higher in the tests with high U residual wastes, and also higher when leached with the CaCO₃-saturated solution than with the Ca(OH)₂-saturated solution. Technetium leachability is not as strongly dependent on the concentration of Tc in the waste, and it appears to be slightly more leachable by the Ca(OH)₂-saturated solution than by the CaCO₃-saturated solution. In general, Tc is much less leachable (<10 wt.% of the available mass in the waste) than previously predicted. This may be due to the coprecipitation of trace concentrations of Tc in relatively insoluble phases such as Fe oxide/hydroxide solids.  相似文献