Bulk modulus of Fe-rich olivines corrected for non-hydrostaticity

In situ X-ray diffraction was used to measure the isothermal bulk modulus at room conditions (K_T0) of synthetic olivines with different iron contents. The chemical formulae of the olivine samples were ${({\mathrm{Fe}}_x,{\mathrm{Mg}}_{1?x})}_2\mathrm{Si}{\mathrm{O}}_4$ with x = 0.45; 0.64; 0.82; 1, with 1% standard deviation (referenced as Fa45, Fa64, Fa82 and Fa100, respectively). All experiments were performed in the multi-anvil apparatus installed at NSLS beamline X17B2, to pressures up to about 7 GPa. Unit-cell volumes under hydrostatic conditions and differential stresses present in the samples were calculated using the method developed by Singh et al. (1998), and pressures measured using NaCl as a standard were then corrected for these stresses. Using a second-order Birch–Murnaghan equation of state, we obtained the isothermal bulk modulus of each composition: $K_{T0}^{\mathrm{Fa45}}=131.4\pm 2.6$ GPa, $K_{T0}^{\mathrm{Fa64}}=132.1\pm 3.1$ GPa, $K_{T0}^{\mathrm{Fa82}}=136.3\pm 1.7$ GPa and $K_{T0}^{\mathrm{Fa100}}=134.8\pm 1.4$ GPa. These values combined with data available in the literature show that the K_T0 of Fe-rich olivines increases very slowly with the Fe content, but possibly not in a simple linear trend.     

Model reconstruction of nitrate pollution of riverbank filtration using 15N and 18O data,Karany, Czech Republic

Stable isotopes of O (δ¹⁸O) in water and N (δ¹⁵N) in ${\text{NO}}_3^{-}$ have been used as natural indigenous groundwater tracers for sources of water and of ${\text{NO}}_3^{-}$ at two riverbank filtration (RBF) water supply systems. Both RBF systems (Skorkov and Sojovice) have wells in unconsolidated Quaternary sediments close to the Jizera River (Czech Republic) that have been affected by increasing ${\text{NO}}_3^{-}$ concentrations. The area is underlain by Turonian sandstones and marls that form a deeper bedrock aquifer. Sources of ${\text{NO}}_3^{-}$ are local sewerage systems and landfills (point sources) and seasonal application of manure and inorganic fertilizers (diffuse sources).At RBF Skorkov recharge to wells can be modelled using a two-component model with 60% river water contribution and 40% of very shallow groundwater with an average residence time of one month. During periods of abundant precipitation, groundwater originates entirely from the unsaturated zone of the Quaternary aquifer; extensive pumping for over 40 a has created new, bypassing flow paths that preferentially drain the contaminated unsaturated zone. During dry periods, wells are recharged by longer residence time groundwater from the Quaternary aquifer.At RBF Sojovice there is an additional recharge component of groundwater from the Turonian aquifer, which is sandier at this locality; this contains denitrified ${\text{NO}}_3^{-}$ with highly positive δ¹⁵N values.     

The measurement of D/H ratio in alkenones and their isotopic heterogeneity

Previous paleoenvironmental studies reported the δD values of a mixture of coeluting alkenones. Here, we present a semi-preparative normal-phase high-performance liquid chromatography–mass spectrometry (NP-HPLC–MS) method for purifying long chain (C₃₇ and C₃₈) unsaturated methyl and ethyl ketones (alkenones) on the basis of chain length and degree of unsaturation.The method was applied to purify alkenones in suspended particles and surface sediments from a site in Chesapeake Bay, eastern USA. The hydrogen isotopic composition of di- and triunsaturated C₃₇ and C₃₈ alkenones differed significantly on the basis of chain length and the degree of unsaturation, demonstrating the importance of gas chromatography–isotope ratio-mass spectrometry (GC–irMS) analysis of individual alkenones for accurate paleoenvironmental reconstruction. Constant fractionation factors between alkenones with different chain length but the same degree of unsaturation (${\alpha }_{{\text{C}}_{37:2}''–''{\text{C}}_{38:2}}\text{and}{\alpha }_{{\text{C}}_{37:3}''–''{\text{C}}_{38:3}}=1.01$) and those with the same chain length but different degree of unsaturation (${\alpha }_{{\text{C}}_{37:2}''–''{\text{C}}_{37:3}}\text{and}{\alpha }_{{\text{C}}_{38:2}''–''{\text{C}}_{38:3}}=0.97$) in all samples suggest that the values may represent hydrogen isotope fractionation associated with elongation and desaturation during alkenone biosynthesis.     

Geochemistry of surface and ground water in Guiyang,China: Water/rock interaction and pollution in a karst hydrological system

The chemical compositions of the surface/ground water of Guiyang, the capital city of Guizhou Province, China are dominated by Ca²⁺, Mg²⁺, ${\text{HCO}}_3^{-}\text{and}{\text{SO}}_4^{2-}$, which have been derived largely from chemical weathering of carbonate rocks (limestone and dolomite). The production of ${\text{SO}}_4^{2-}$ has multiple origins, mainly from dissolution of sulfate evaporites, oxidation of sulfide minerals and organic S in the strata, and anthropogenic sources. Most ground water is exposed to soil CO₂ and, therefore, the H₂CO₃ which attacks minerals contains much soil C. In addition, the H₂SO₄ produced as a result of the oxidation of sulfides in S-rich coal seams and/or organic S, is believed to be associated with the chemical weathering of rocks. The major anthropogenic components in the surface and ground water include K⁺, Na⁺, Cl⁻, ${\text{SO}}_4^{2-}\text{and}{\text{NO}}_3^{-}$, with Cl⁻ and ${\text{NO}}_3^{-}$ being the main contributors to ground water pollution in Guiyang and its adjacent areas. The seasonal variations in concentrations of anthropogenic components demonstrate that the karst ground water system is liable to pollution by human activities. The higher content of ${\text{NO}}_3^{-}$ in ground water compared to surface water during the summer and winter seasons, indicates that the karstic ground water system is not capable of denitrification and therefore does not easily recover once contaminated with nitrates.     

Applications of Mango’s light hydrocarbon parameters to petroleum from Tarim basin,NW China

Light hydrocarbons in oils from the Tarim basin, NW China, were analyzed by GC. The light hydrocarbon parameters proposed by Mango revealed the distributions of the oils as two main types, marine and terrigenous sources. The Mango parameter K₁ not only displays a remarkable invariance (∼1) in most of the oils, but also shows significant variations (ranging from 1.20 to 1.54) in the oils occurring in the eastern part of the Tazhong Fault Uplift (EPTFU) located in the center of the Tarim basin. This variation of the K₁ value may indicate different petroleum systems in the areas which are superimposed in the EPTFU. Parameter K₂ proposed by Mango shows a significant variation between the two main oil types. The marine oils are characterized by relatively low values of K₂ (average 0.23) and the terrigenous oils by relatively high K₂ values (average 0.35), with general invariance within the same oil set. A plot of (P₃ + P₂ + N₂) vs. $(N_1^6)$ based on the model proposed by Mango can be used not only to discriminate between the two main genetic oils from the Tarim basin, but also to classify the marine oils from the Lunnan area into two sub-types, which may indicate two sub-petroleum systems existing in the area.