Assessing the Vibrational Frequencies of the Holweide Hospital in the City of Cologne (Germany) by Means of Ambient Seismic Noise Analysis and FE modelling

Ambient seismic noise measurements were conducted inside the Holweide Hospital (Cologne) for checking whether its frequencies of vibration fall into the range where soil amplification is expected. If this is the case, damage might increase in case of an earthquake due to an amplified structural response of the building. Two different techniques were used: the ratio between the horizontal and vertical components of the spectra recorded at stations located inside the building and the ratio between the corresponding components of the spectra recorded simultaneously inside the building and at a reference station placed outside. While the former method might be preferred because of less equipment involved, the latter has the advantage of producing more stable results and deleting automatically the influence of the sedimentary cover, which might obscure some eigenfrequencies of vibration of the building. An independently performed finite-element analysis of the hospital showed a good correlation between measured and calculated eigenmodes.     

Ab initio study of the high-pressure behavior of CaSiO3 perovskite

Using density functional simulations, within the generalized gradient approximation and projector-augmented wave method, we study structures and energetics of CaSiO₃ perovskite in the pressure range of the Earths lower mantle (0–150 GPa). At zero Kelvin temperature the cubic CaSiO₃ perovskite structure is unstable in the whole pressure range, at low pressures the orthorhombic (Pnam) structure is preferred. At 14.2 GPa there is a phase transition to the tetragonal (I4/mcm) phase. The CaIrO₃-type structure is not stable for CaSiO₃. Our results also rule out the possibility of decomposition into oxides.

δ34S isotope values of dissolved sulfate (SO4 2−) as a tracer for battery acid (H2SO4) contamination in groundwater

The application of sulfur isotope (³⁴S) values of sulfate in groundwater provided the information necessary to evaluate the source, transport and fate of battery acid and associated contaminants at the Gulf Coast Recycling (GCR) facility. The chemical and isotopic composition of groundwater beneath the (GCR) property, a battery recycling facility in east Tampa, Florida, varies more than expected for an area of comparable size. Sulfate (SO₄^2–) values, for example, range from 1.2 to 11,500 mg/L and oxygen and hydrogen isotopes do not attenuate towards the weighted annual mean. Those samples that are high in sulfate generally have a low pH, which immediately indicates battery acid (H₂SO₄) contamination as a potential source for the sulfate. The low pH and high reactivity of the sulfuric acid groundwater cause the formation of hydrogeological microenvironments due to preferential dissolution of carbonate minerals, which in turn causes enhanced recharge and groundwater flow in certain areas; thus, the extreme scatter in the data set. Because of the difficult hydrogeology it is not straightforward to delineate the point-sources of contamination and up to five potential scenarios have to be evaluated: (1) seawater intrusion, (2) upwelling of high-sulfate groundwater, (3) local dissolution of gypsum, (4) an up-gradient contaminant source to the northeast of the GCR property and (5) battery acid contamination.     

CO<Subscript>2</Subscript> Air–Sea Exchange due to Calcium Carbonate and Organic Matter Storage,and its Implications for the Global Carbon Cycle

Release of CO₂ from surface ocean water owing to precipitation of CaCO₃ and the imbalance between biological production of organic matter and its respiration, and their net removal from surface water to sedimentary storage was studied by means of a quotient θ = (CO₂ flux to the atmosphere)/(CaCO₃ precipitated). θ depends not only on water temperature and atmospheric CO₂ concentration but also on the CaCO₃ and organic carbon masses formed. In CO₂ generation by CaCO₃ precipitation, θ varies from a fraction of 0.44 to 0.79, increasing with decreasing temperature (25 to 5°C), increasing atmospheric CO₂ concentration (195–375 ppmv), and increasing CaCO₃ precipitated mass (up to 45% of the initial DIC concentration in surface water). Primary production and net storage of organic carbon counteracts the CO₂ production by carbonate precipitation and it results in lower CO₂ emissions from the surface layer. When atmospheric CO₂ increases due to the ocean-to-atmosphere flux rather than remaining constant, the amount of CO₂ transferred is a non-linear function of the surface layer thickness because of the back-pressure of the rising atmospheric CO₂. For a surface ocean layer approximated by a 50-m-thick euphotic zone that receives input of inorganic and organic carbon from land, the calculated CO₂ flux to the atmosphere is a function of the CaCO₃ and C_org net storage rates. In general, the carbonate storage rate has been greater than that of organic carbon. The CO₂ flux near the Last Glacial Maximum is 17 to 7×10¹² mol/yr (0.2–0.08 Gt C/yr), reflecting the range of organic carbon storage rates in sediments, and for pre-industrial time it is 38–42×10¹² mol/yr (0.46–0.50 Gt C/yr). Within the imbalanced global carbon cycle, our estimates indicate that prior to anthropogenic emissions of CO₂ to the atmosphere the land organic reservoir was gaining carbon and the surface ocean was losing carbon, calcium, and total alkalinity owing to the CaCO₃ storage and consequent emission of CO₂. These results are in agreement with the conclusions of a number of other investigators. As the CO₂ uptake in mineral weathering is a major flux in the global carbon cycle, the CO₂ weathering pathway that originates in the CO₂ produced by remineralization of soil humus rather than by direct uptake from the atmosphere may reduce the relatively large imbalances of the atmosphere and land organic reservoir at 10²–10⁴-year time scales.     

Evidence for Co-Propagation of 4765- and 1720-MHz OH Masers in Star-Forming Regions

Two star-forming regions Cepheus A and W75N, were searched for the 4765-MHz OH maser emission using the multi-element radio linked interferometer network (MERLIN). The excited OH emission has an arc-like structure of 40 mas in Cep A and a linear structure of size 45 mas in W75N. We also found the 1720-MHz line in Cep A and Hutawarakorn [MNRAS 330 (2002) 349] reported the 1720-MHz emission in W75N. The 1720- and 4765-MHz OH spots coincided in space within 60 mas and in velocity within 0.3 km s^–1 in both targets implying that both maser transitions arise from the same region. According to the modelling by Gray [MNRAS 252 (1991) 30] the 1720/4765-MHz co-propagation requires a low density, warm environment. The masers lie at the edges of H II regions where such conditions are expected.     

Discovery of double-peaking potassic volcanic rocks in Langshan Group of the Tanyaokou hydrothermal-sedimentary deposit,Inner Mongolia,and its indicating significance

Since the mid-1980s,Tanyaokou large Zn-Cu-Fe sulfides deposit,located at the southwest end of Langshan-Zhaertaishan-Bayan Obo Mesoproterozoic metallogenic belt in the west section of the northern margin of the North China Platform[1?9](Fig.1),has been confirmed to be submarine volcanic exhalative-sedimentary metamorphosed deposit hosted in the miogeosynclinal mud-carbonaceous formation of the Langshan Group(LG)[1],or submarine volcanic exha-lative-deposition-altered deposit[2]or stratabo…     

Ionic association in H2O–CO2 fluids at mid-crustal conditions

The equilibrium constant, K _a, of the association reaction to form ion pairs from charged solute species in supercritical solutions can be calculated from a model based on published equations. Log K _a at constant pressure is a linear function of the inverse in the dielectric constant of the fluid times temperature. The dielectric properties of H₂O and CO₂ at supercritical pressures and temperatures can also be evaluated using the Kirkwood equation. Using Looyenga mixing rules, the dielectric constant of H₂O–CO₂ mixtures can be obtained and the change in log K _a with addition of CO₂ in aqueous solutions evaluated. These changes in log K _a with addition of CO₂ are consistent with measured changes of log K _a with addition of Ar in supercritical H₂O–Ar solutions.
Log K _a of KCl and NaCl increase to an increasing extent as the mole fraction of CO₂ increases in H₂O–CO₂ solutions. For instance, at 2 kbar and constant temperature between 400 and 600° C, log K _a of KCl increases by about two orders of magnitude whilst that of NaCl increases by over four orders of magnitude as the CO₂ mole fraction increases from 0.0 to 0.35. Such changes in log K _a will have dramatic effects on the solubility of minerals in CO₂-rich environments.     

Theory of Basin Scale Dynamics of a Stratified Rotating Fluid

The dynamics of a stratified fluid contained in a rotating rectangular box is described in terms of the evolution of the lowest moments of its density and momentum fields. The first moment of the density field also gives the position of the fluids centre-of-mass. The resulting low-order model allows for fast assessment both of adopted parameterisations, as well as of particular values of parameters. In the ideal fluid limit (neglect of viscous and diffusive effects), in the absence of wind, the equations have a Hamiltonian structure that is integrable (non-integrable) in the absence (presence) of differential heating. In a non-rotating convective regime, dynamically rich behaviour and strong dependence on the single (lumped) parameter are established. For small values of this parameter, in a self-similar regime, further reduction to an explicit map is discussed in an Appendix. Introducing rotation in a nearly geostrophic regime leads through a Hopf bifurcation to a limit cycle, and under the influence of wind and salt to multiple equilibria and chaos, respectively.     

Kinetics and Equilibrium Sorption Studies of 4-Nitrophenol on pyrolyzed and activated oil shale residue

Sorption of the organic pollutant 4-nitrophenol (4-NP) by pyrolyzed and activated Jordanian oil-shale was studied. Pyrolyzed oil shale was prepared using a fluidized bed reactor at 520 °C in the presence of nitrogen. Physical activation was carried out by treating the pyrolyzed oil shale with CO₂ at 830 °C, while chemical activation was achieved by using KOH and ZnCl₂ as impregnating agents. Batch kinetics and isotherm studies were conducted to evaluate the sorption process. Effects of contact time, initial sorbate concentration, sorbent concentration, temperature, pH and inorganic salts (NaCl and KCl) on the sorption process by the different sorbents were considered. Chemically activated oil shale, pretreated with ZnCl₂, gave the highest uptake of 4-NP. The isotherm experimental data fit reasonably well to Langmuir, Freundlich and Redlich-Paterson models. Three kinetic models, namely the Morris-Weber, Lagergren, and Pseudo-Second-Order model (PSOM), were applied to represent the experimental results for both pyrolyzed and ZnCl₂-oil shale sorbents.     

A technique for modeling the Earth’s gravity field on the basis of satellite accelerations

A technique is proposed for Earths gravity field modeling on the basis of satellite accelerations that are derived from precise orbit data. The functional model rests on Newtons second law. The computational procedure is based on the pre-conditioned conjugate-gradient (PCCG) method. The data are treated as weighted average accelerations rather than as point-wise ones. As a result, a simple three-point numerical differentiation scheme can be used to derive them. Noise in the orbit-derived accelerations is strongly dependent on frequency. Therefore, the key element of the proposed technique is frequency-dependent data weighting. Fast convergence of the PCCG procedure is ensured by a block-diagonal pre-conditioner (approximation of the normal matrix), which is derived under the so-called Colombo assumptions. Both uninterrupted data sets and data with gaps can be handled. The developed technique is compared with other approaches: (1) the energy balance approach (based on the energy conservation law) and (2) the traditional approach (based on the integration of variational equations). Theoretical considerations, supported by a numerical study, show that the proposed technique is more accurate than the energy balance approach and leads to approximately the same results as the traditional one. The former finding is explained by the fact that the energy balance approach is only sensitive to the along-track force component. Information about the cross-track and the radial component of the gravitational potential gradient is lost because the corresponding force components do no work and do not contribute to the energy balance. Furthermore, it is shown that the proposed technique is much (possibly, orders of magnitude) faster than the traditional one because it does not require the computation of the normal matrix. Hints are given on how the proposed technique can be adapted to the explicit assembling of the normal matrix if the latter is needed for the computation of the model covariance matrix.Acknowledgments. Professor R. Klees is thanked for support of the project and for numerous fruitful discussions. The authors are also thankful to Dr. J. Kusche for useful remarks and to Dr. E. Schrama, his solid background in satellite geodesy proved to be very helpful. A large number of valuable comments were made by Dr. S.-C. Han, Dr. P. Schwintzer, and an anonymous reviewer; their contribution is greatly acknowledged. The satellite orbits used in the numerical study were kindly provided by Dr. P. Visser (Aerospace Department, Delft University of Technology). Access to the SGI Origin 3800 computer was provided by Stichting Nationale Computerfaciliteiten (NCF), grant SG-027.