The stiff upper LIP: investigating the High Arctic Large Igneous Province     

F.M. Deegan  V.R. Troll  J.H. Bédard  C.A. Evenchick  K. Dewing  S. Grasby  H. Geiger  C. Freda  V. Misiti  S. Mollo 《Geology Today》2016,32(3):92-98

The Canadian Arctic Islands expose a complex network of dykes and sills that belong to the High Arctic Large Igneous Province (HALIP), which intruded volatile‐rich sedimentary rocks of the Sverdrup Basin (shale, limestone, sandstone and evaporite) some 130 to 120 million years ago. There is thus great potential in studying the HALIP to learn how volatile‐rich sedimentary rocks respond to magmatic heating events during LIP emplacement. The HALIP remains, however, one of the least well known LIPs on the planet due to its remote location, short field season, and harsh climate. A Canadian–Swedish team of geologists set out in summer 2015 to further explore HALIP sills and their sedimentary host rocks, including the sampling of igneous and meta‐sedimentary rocks for subsequent geochemical analysis, and high pressure‐temperature petrological experiments to help define the actual processes and time‐scales of magma–sediment interaction. The research results will advance our understanding of how climate‐active volatiles such as CO_2, SO₂ and CH₄ are mobilised during the magma–sediment interaction related to LIP events, a process which is hypothesised to have drastically affected Earth's carbon and sulphur cycles. In addition, assimilation of sulphate evaporites, for example, is anticipated to trigger sulphide immiscibility in the magma bodies and in so doing could promote the formation of Ni‐PGE ore bodies. Here we document the joys and challenges of ‘frontier arctic fieldwork’ and discuss some of our initial observations from the High Arctic Large Igneous Province.  相似文献   

Exponential time integrators for stochastic partial differential equations in 3D reservoir simulation     

Sebastian Geiger  Gabriel Lord  Antoine Tambue 《Computational Geosciences》2012,16(2):323-334

The transport of chemically reactive solutes (e.g. surfactants, CO₂ or dissolved minerals) is of fundamental importance to a wide range of applications in oil and gas reservoirs such as enhanced oil recovery and mineral scale formation. In this work, we investigate exponential time integrators, in conjunction with an upwind weighted finite volume discretisation in space, for the efficient and accurate simulation of advection–dispersion processes including non-linear chemical reactions in highly heterogeneous 3D oil reservoirs. We model sub-grid fluctuations in transport velocities and uncertainty in the reaction term by writing the advection–dispersion–reaction equation as a stochastic partial differential equation with multiplicative noise. The exponential integrators are based on the variation of constants solution and solve the linear system exactly. While this is at the expense of computing the exponential of the stiff matrix representing the finite volume discretisation, the use of real Léja point or the Krylov subspace technique to approximate the exponential makes these methods competitive compared to standard finite difference-based time integrators. For the deterministic system, we investigate two exponential time integrators, the second-order accurate exponential Euler midpoint (EEM) scheme and exponential time differencing of order one (ETD1). All our numerical examples demonstrate that our methods can compete in terms of efficiency and accuracy compared with standard first-order semi-implicit time integrators when solving (stochastic) partial differential equations that model mixing and chemical reactions in 3D heterogeneous porous media. Our results suggest that exponential time integrators such as the ETD1 and EEM schemes could be applied to typical 3D reservoir models comprising tens to hundreds of thousands unknowns.  相似文献   

A temperature dependent X-ray Absorption Fine Structure study of dynamic X-site disorder in almandine: a comparison to diffraction data     

Simona Quartieri  G. Antonioli  G. Artioli  C. A. Geiger  P. P. Lottici 《Physics and Chemistry of Minerals》1997,24(3):200-205

X-ray Absorption Fine-Structure (XAFS) measurements in the temperature range 20-473K at the Fe K-edge of synthetic almandine (Fe₃Al₂Si₃O₁₂) allow us to determine the temperature dependence of the XAFS Debye-Waller (DW) factors for each of the two crystallographically independent Fe?O bond distances (Fe(1)?O and Fe(2)?O). The vibrational anisotropy of Fe²⁺ in the dodecahedral X-site has been documented. The XAFS DW factor of the longer Fe(2)?O bond is larger and has a greater T-dependence than the shorter Fe(1)?O bond, which remains constant over the measured T range. The XAFS DW factors are compared with the uncorrelated part of the DW factors derived from a single-crystal X-ray diffraction (XRD) study on almandine and are interpreted on the basis of the Einstein model. A comparison with diffraction data shows that the shorter Fe(1)–O bond is significantly affected by correlation in the atomic displacements.  相似文献   

Crustal motion and deformation in Greece from a decade of GPS measurements, 1993–2003   总被引：1，自引：1，他引：0  

Ch. Hollenstein  M.D. Müller  A. Geiger  H.-G. Kahle   《Tectonophysics》2008,449(1-4):17-40

The Hellenic plate boundary region, located in the collision zone between the Nubian/Arabian and Eurasian lithospheric plates, is one of the seismo-tectonically most active areas of Europe. During the last 15 years, GPS measurements have been used to determine the crustal motion in the area of Greece with the aim to better understand the geodynamical processes of this region. An extended reoccupation network covering whole Greece has been measured periodically in numerous GPS campaigns since the late eighties, and a continuous GPS network has been operated in the region of the Ionian Sea since 1995. In this paper, we present a new detailed high-quality solution of continuous and campaign-type measurements acquired between 1993 and 2003. During the GPS processing, a special effort was made to obtain consistent results with highest possible accuracies and reliabilities. Data of 54 mainly European IGS and EUREF sites were included in the GPS processing in order to obtain results which are internally consistent with the European kinematic field and order to allow for a regional interpretation. After an overview of the results of the IGS/EUREF sites, the results from more than 80 stations in Greece are presented in terms of velocities, time series, trajectories and strain rates. Previous geodetic, geological and seismological findings are generally confirmed and substantially refined. New important results include the observation of deformation zones to the north and to the south of the North Aegean Trough and in the West Hellenic arc region, arc-parallel extension of about 19 mm/yr along the Hellenic arc, and compression between the Ionian islands and the Greek mainland. Due to continuous long-term observations of 4–8 years, it was possible to extract height changes from the GPS time series. In Greece, we observe a differential subsidence of the order of 2 mm/yr between the northern and central Ionian islands across the Kefalonia fault zone. The differential subsidence of the central Ionian islands with respect to the northwestern Greek mainland amounts to 4 mm/yr.  相似文献   

Tropospheric refractivity and zenith path delays from least-squares collocation of meteorological and GNSS data   总被引：1，自引：0，他引：1  

Karina Wilgan  Fabian Hurter  Alain Geiger  Witold Rohm  Jarosław Bosy 《Journal of Geodesy》2017,91(2):117-134

Precise positioning requires an accurate a priori troposphere model to enhance the solution quality. Several empirical models are available, but they may not properly characterize the state of troposphere, especially in severe weather conditions. Another possible solution is to use regional troposphere models based on real-time or near-real time measurements. In this study, we present the total refractivity and zenith total delay (ZTD) models based on a numerical weather prediction (NWP) model, Global Navigation Satellite System (GNSS) data and ground-based meteorological observations. We reconstruct the total refractivity profiles over the western part of Switzerland and the total refractivity profiles as well as ZTDs over Poland using the least-squares collocation software COMEDIE (Collocation of Meteorological Data for Interpretation and Estimation of Tropospheric Pathdelays) developed at ETH Zürich. In these two case studies, profiles of the total refractivity and ZTDs are calculated from different data sets. For Switzerland, the data set with the best agreement with the reference radiosonde (RS) measurements is the combination of ground-based meteorological observations and GNSS ZTDs. Introducing the horizontal gradients does not improve the vertical interpolation, and results in slightly larger biases and standard deviations. For Poland, the data set based on meteorological parameters from the NWP Weather Research and Forecasting (WRF) model and from a combination of the NWP model and GNSS ZTDs shows the best agreement with the reference RS data. In terms of ZTD, the combined NWP-GNSS observations and GNSS-only data set exhibit the best accuracy with an average bias (from all stations) of 3.7 mm and average standard deviations of 17.0 mm w.r.t. the reference GNSS stations.  相似文献   

Molecular H₂O in armenite, BaCa₂Al₆Si₉O₃₀·2H₂O, and epididymite, Na₂Be₂Si₆O₁₅·H₂O: Heat capacity, entropy and local-bonding behavior of confined H₂O in microporous silicates     

Charles A. Geiger  Edgar Dachs  Gilberto Artioli 《Geochimica et cosmochimica acta》2010,74(18):5202-5215

Armenite, ideal formula BaCa₂Al₆Si₉O₃₀·2H₂O, and its dehydrated analog BaCa₂Al₆Si₉O₃₀ and epididymite, ideal formula Na₂Be₂Si₆O₁₅·H₂O, and its dehydrated analog Na₂Be₂Si₆O₁₅ were studied by low-temperature relaxation calorimetry between 5 and 300 K to determine the heat capacity, C_p, behavior of their confined H₂O. Differential thermal analysis and thermogravimetry measurements, FTIR spectroscopy, electron microprobe analysis and powder Rietveld refinements were undertaken to characterize the phases and the local environment around the H₂O molecule.The determined structural formula for armenite is Ba_0.88(0.01)Ca_1.99(0.02)Na_0.04(0.01)Al_5.89(0.03)Si_9.12(0.02)O₃₀·2H₂O and for epididymite Na_1.88(0.03)K_0.05(0.004)Na_0.01(0.004)Be_2.02(0.008)Si_6.00(0.01)O₁₅·H₂O. The infrared (IR) spectra give information on the nature of the H₂O molecules in the natural phases via their H₂O stretching and bending vibrations, which in the case of epididymite only could be assigned. The powder X-ray diffraction data show that armenite and its dehydrated analog have similar structures, whereas in the case of epididymite there are structural differences between the natural and dehydrated phases. This is also reflected in the lattice IR mode behavior, as observed for the natural phases and the H₂O-free phases. The standard entropy at 298 K for armenite is S° = 795.7 ± 6.2 J/mol K and its dehydrated analog is S° = 737.0 ± 6.2 J/mol K. For epididymite S° = 425.7 ± 4.1 J/mol K was obtained and its dehydrated analog has S° = 372.5 ± 5.0 J/mol K. The heat capacity and entropy of dehydration at 298 K are Δ = 3.4 J/mol K and ΔS^rxn = 319.1 J/mol K and Δ = −14.3 J/mol K and ΔS^rxn = 135.7 J/mol K for armenite and epididymite, respectively. The H₂O molecules in both phases appear to be ordered. They are held in place via an ion-dipole interaction between the H₂O molecule and a Ca cation in the case of armenite and a Na cation in epididymite and through hydrogen-bonding between the H₂O molecule and oxygen atoms of the respective silicate frameworks. Of the three different H₂O phases ice, liquid water and steam, the C_p behavior of confined H₂O in both armenite and epididymite is most similar to that of ice, but there are differences between the two silicates and from the C_p behavior of ice. Hydrogen-bonding behavior and its relation to the entropy of confined H₂O at 298 K is analyzed for various microporous silicates.The entropy of confined H₂O at 298 K in various silicates increases approximately linearly with increasing average wavenumber of the OH-stretching vibrations. The interpretation is that decreased hydrogen-bonding strength between a H₂O molecule and the silicate framework, as well as weak ion-dipole interactions, results in increased entropy of H₂O. This results in increased amplitudes of external H₂O vibrations, especially translations of the molecule, and they contribute strongly to the entropy of confined H₂O at T < 298 K.  相似文献   

<Superscript>57</Superscript>Fe Mössbauer measurements and electronic structure calculations on natural lawsonites     

S.-U. Weber  M. Grodzicki  C. A. Geiger  W. Lottermoser  G. Tippelt  G. J. Redhammer  M. Bernroider  G. Amthauer 《Physics and Chemistry of Minerals》2007,34(1):1-9

Three natural lawsonites from Syke Rock, Mendocino Co., Reed Ranch, Marin Co., and Blake Gardens, Sonoma Co., all from the Coast Range Region in California, were studied by ⁵⁷Fe Mössbauer spectroscopy, electron microprobe analysis, and X-ray powder diffraction. The samples contain about 0.6, 1.0, and 1.4 wt% of total iron oxide, respectively. ⁵⁷Fe Mössbauer spectra are consistent with the assumption that high-spin Fe³⁺ substitutes for Al in the octahedrally coordinated site. The Mössbauer spectrum of lawsonite from Syke Rock exhibits a second doublet with ⁵⁷Fe hyperfine parameters typical for octahedrally coordinated high-spin Fe²⁺. Electronic structure calculations in the local spin density approximation yield quadrupole splittings for Fe³⁺ in quantitative agreement with experiment indicating, however, that substitution of Al by Fe³⁺ must be accompanied by local distortion around the octahedral site. Model calculations also reproduce the room temperature hyperfine parameters of ferrous high-spin iron assuming the substitution of Ca by Fe²⁺. However, it cannot be excluded that Fe²⁺ may occupy a more asymmetric site within the microstructural cavity occupied by Ca and a H₂O molecule.  相似文献   

The Chemical Quality of Self-Supplied Domestic Well Water in the United States     

Michael J. Focazio  Deborah Tipton  Stephanie Dunkle Shapiro  Linda H. Geiger 《Ground Water Monitoring & Remediation》2006,26(3):92-104

  相似文献   

Chemical Mechanism Development: Laboratory Studies and Model Applications     

Harald Geiger  Ian Barnes  Karl H. Becker  Birger Bohn  Theo Brauers  Birgit Donner  Hans-Peter Dorn  Manfred Elend  Carlos M. Freitas Dinis  Dirk Grossmann  Heinz Hass  Holger Hein  Axel Hoffmann  Lars Hoppe  Frank Hülsemann  Dieter Kley  Björn Klotz  Hans G. Libuda  Tobias Maurer  Djuro Mihelcic  Geert K. Moortgat  Romeo Olariu  Peter Neeb  Dirk Poppe  Lars Ruppert  Claudia G. Sauer  Oleg Shestakov  Holger Somnitz  William R. Stockwell  Lars P. Thüner  Andreas Wahner  Peter Wiesen  Friedhelm Zabel  Reinhard Zellner  Cornelius Zetzsch 《Journal of Atmospheric Chemistry》2002,42(1):323-357

Within the German Tropospheric Research Programme (TFS) numerous kinetic and mechanistic studies on the tropospheric reaction/degradation of the following reactants were carried out: oxygenated VOC, aromatic VOC, biogenic VOC, short-lived intermediates, such as alkoxy and alkylperoxy radicals.At the conception of the projects these selected groups were classes of VOC or intermediates for which the atmospheric oxidation mechanisms were either poorly characterised or totally unknown. The motivation for these studies was the attainment of significant improvements in our understanding of the atmospheric chemical oxidation processes of these compounds, particularly with respect to their involvement in photooxidant formation in the troposphere. In the present paper the types of experimental investigations performed and the results obtained within the various projects are briefly summarised. The major achievements are highlighted and discussed in terms of their contribution to improving our understanding of the chemical processes controlling photosmog formation in the troposphere.  相似文献   

The orientation and vibrational states of H2O in synthetic alkali-free beryl     

B. A. Kolesov  C. A. Geiger 《Physics and Chemistry of Minerals》2000,27(8):557-564

 The polarized single-crystal Raman spectra of synthetic H₂O-containing alkali-free beryl were recorded at room and low temperatures, and the polarized single-crystal IR spectra at room temperature. The H₂O molecule in the channel cavities is characterized by a Raman-active symmetric stretching vibration (ν₁) at 3607 cm⁻¹ and an IR-active asymmetric stretch (ν₃) at 3700 cm⁻¹ at room temperature. At low temperatures this ν₃ mode is observed in the Raman. Weak ν₁ and ν₃ modes of a second type of H₂O are also observed in the Raman spectra but only at 5 K. The H⋯&middot;H vector of the most abundant type of H₂O is parallel to the channel axis of beryl along [0 0 0 1]. The components of the polarizability tensor of the ν₁ mode of H₂O are similar to, but not exactly the same as, those of a free H₂O molecule. The Raman measurements indicate that the H₂O molecule is rotationally disordered around [0 0 0 1]. External translation and librational modes of H₂O could be observed as overtones with the internal H₂O-stretching modes. In the case of the librational motions, normal modes could also be observed directly in the Raman spectra at ∼200 cm⁻¹. The energies of the translational modes can be determined from an analysis of the overtones and are about 9 cm⁻¹ in energy (i.e., T_z). The energies of the librational modes are about 210 cm⁻¹ for R_x and 190 cm⁻¹ for R_y. Received: 8 April 1999 / Accepted: 5 April 2000  相似文献