Melting of corundum using conventional and two-phase molecular dynamic simulation method

The melting curve of corundum is calculated by using two approaches: the first one is conventional and the second one is two-phase molecular dynamics method both utilizing the same pairwise interatomic potential developed earlier on. The melting curve obtained by the two-phase simulation method is in agreement with the existing experimental data up to 25 GPa. A comparison of melting curves obtained by a two-phase simulation method and a conventional molecular dynamic method in NPT ensemble demonstrates a substantial overestimation of melting temperatures when applying conventional molecular dynamic technique. The inaccuracy of the conventional method increases with increasing pressure and, in the case of corundum, changes from about 300 K at 1 bar to about 1000 K at 1 Mbar. Received: 25 November 1996 / Revised, accepted: 11 March 1997     

In‐Situ Sonication for Enhanced Recovery of Aquifer Microbial Communities

Sampling methods for characterization of microbial communities in aquifers should target both suspended and attached microorganisms (biofilms). We investigated the effectiveness and reproducibility of low‐frequency (200 Hz) sonication pulses on improving extraction efficiency and quality of microorganisms from a petroleum‐contaminated aquifer in Studen (Switzerland). Sonication pulses at different power levels (0.65, 0.9, and 1.1 kW) were applied to three different groundwater monitoring wells. Groundwater samples extracted after each pulse were compared with background groundwater samples for cell and adenosine tri‐phosphate concentration. Turbidity values were obtained to assess the release of sediment fines and associated microorganisms. The bacterial community in extracted groundwater samples was analyzed by terminal‐restriction‐fragment‐length polymorphism and compared with communities obtained from background groundwater samples and from sediment cores. Sonication enhanced the extraction efficiency up to 13‐fold, with most of the biomass being associated with the sediment fines extracted with groundwater. Consecutive pulses at constant power were decreasingly effective, while pulses with higher power yielded the best results both in terms of extraction efficiency and quality. Our results indicate that low‐frequency sonication may be a viable and cost‐effective tool to improve the extraction of microorganisms from aquifers, taking advantage of existing groundwater monitoring wells.     

Injection and arrest of dykes: implications for volcanic hazards

Dykes are the principal channels through which magma reaches the surface in volcanic eruptions. For this reason dykes observed in the field are commonly assumed to be feeders to lava flows. The actual proportion of dykes reaching the surface is, however, poorly known. In order to develop models for the purpose of estimating volcanic hazard, this proportion must be known. This follows because such models should not only consider the probability of dykes being injected from magma chambers during periods of unrest in the associated volcanoes, but also the probability of the injected dykes being arrested. This paper presents field data on several thousand dykes from Iceland and Tenerife (Canary Islands) indicating that many, and probably most, dykes become arrested at various crustal levels and never reach the surface to feed eruptions. Using the results of analytical and numerical models, it is shown that, for common loading conditions, the stress field in the vicinity of a magma chamber may favour the injection and propagation of dykes while the stress field at a certain distance from the chamber favours dyke arrest. This means that many dykes that are injected from the chamber propagate only for a very limited distance from the chamber to the point where they become arrested. The implication is that during periods of unrest in volcanoes, the probability of volcanic eruption is only a small fraction of the probability of dyke injection from the source magma chamber.     

Correction for distortions of magnetotelluric fields: Limits of validity of the static approach

Subsurface inhomogeneities can be classified in three categories depending on the comparison of their sizes against the effective skin depth and “adjustment distance”. These categories are geological noise, local and regional inhomogeneities. Due to its random nature, geological noise leads to uncontrollable distortions of the magnetotelluric field. Such methods as curve shifting, distortion tensor techniques, decomposition and spatial filtering can effectively be used to correct for static shift caused by geological noise. It is shown that the effects of local and regional subsurface inhomogeneities reduce to static shifts of MT-curves when rather rigid conditions are satisfied. The methods used to suppress the effect of geological noise have limited applicability to local and regional inhomogeneities, which can be accurately accounted for only by modelling.     

Influence of food web structure on the biochemical composition of seston,zooplankton and recently deposited sediment in experimental freshwater mesocosms

The effects of food web structure on the quantity and biochemical composition of seston, zooplankton and recently deposited sediment in experimental freshwater mesocosms were examined. Food web structure was manipulated by addition of zooplanktivorous fish. Biochemical characterisations were carried out using lipid biomarkers (sterols, fatty acids, chlorophyll-derived compounds and long-chain alkanediols). Fish addition decreased zooplankton biomass and increased seston biomass and deposited sediment through a trophic cascade. Fish presence strongly influenced the biochemical characteristics of seston and sediment. In contrast, food web structure had a minor impact on the lipid biomarker composition of zooplankton. Although the relative abundance of sterols in the different compartments did not differ strongly between treatments, sterol profiles in seston and sediment depended on food web structure. The predominance of Δ⁷-sterols in seston and sediment in the fish treatment indicated a major contribution of Chlorophyceae. In contrast, the distribution of sterols in seston and sediment in the fishless treatment, dominated by cholesterol, indicated a major zooplanktonic input. The distribution of fatty acids and the relative abundance of chlorophyll-derived compounds and long-chain alkanediols agreed with the predominant contribution of phytoplankton or zooplankton to seston and sediment in the two treatments. The relative abundance of bacterial biomarkers suggested that the contribution of bacteria was rather low. The high relative abundance of polyunsaturated fatty acids (PUFAs) and the absence of stanols in sediments suggested low microbial reworking of organic matter in the recently accumulated sediments. The trophic cascade, generated by the addition of fish, increased the relative abundance of PUFAs in deposited organic matter, thus enhancing sediment quality and potential degradability.     

Production of selected cosmogenic radionuclides by muons: 2. Capture of negative muons

We have determined the production yields for radionuclides in Al₂O₃, SiO₂, S, Ar, K₂SO₄, CaCO₃, Fe, Ni and Cu targets, which were irradiated with slow negative muons at the Paul Scherrer Institute in Villigen (Switzerland). The fluences of the stopped negative muons were determined by measuring the muonic X-rays. The concentrations of the long-lived and short-lived radionuclides were measured with accelerator mass spectrometry (AMS) and γ-spectroscopy, respectively. Special emphasis was put on the radionuclides ¹⁰Be, ¹⁴C and ²⁶Al produced in quartz targets, ²⁶Al in Al₂O₃ and S targets, ³⁶Cl in K₂SO₄ and CaCO₃ targets, and ⁵³Mn in Fe₂O₃ targets. These targets were selected because they are also the naturally occurring target minerals for cosmic ray interactions in typical rocks. We also present results of calculations for depth-dependent production rates of radionuclides produced after cosmic ray μ⁻ capture, as well as cosmic ray-induced production rates of geologically relevant radionuclides produced by the nucleonic component, by μ⁻ capture, by fast muons and by neutron capture.     

The Central Iberian arc, an orocline centered in the Iberian Massif and some implications for the Variscan belt

An arcuate structure, comparable in size with the Ibero-Armorican arc, is delineated by Variscan folds and magnetic anomalies in the Central Iberian Zone of the Iberian Massif. Called the Central Iberian arc, its sense of curvature is opposite to that of the Ibero-Armorican arc, and its core is occupied by the Galicia-Trás-os-Montes Zone of NW Iberia, which includes the Rheic suture. Other zones of the Iberian Massif are bent by the arc, but the Ossa-Morena and South Portuguese zones are not involved. The arc formed during the Late Carboniferous, at final stages of thermal relaxation and collapse, and an origin related with right-lateral ductile transpression at the scale of the Variscan belt is proposed. The Central Iberian arc explains the width of the Central Iberian Zone, clarifies the position of the allochthonous terranes of NW Iberia, and opens new perspectives for correlations with the rest of the Variscan belt, in particular, with the Armorican Massif, whose central zone represents the continuation of the southwest branch of the arc detached by strike-slip tectonics.     

Experimental Study of Gold and Platinum Solubility in a Complex Fluid under Hydrothermal Conditions

Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log m_Au–m_NaCl–T frame fixed linear dependence between log m_Au and T at any studied iso‐pleth (m_NaCl) in the form of log m_Au = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log m_Au) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied f_O2/f_S2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower f_O2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H₂O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H₂O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 m_HCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log m_Pt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)₂ and Mn₂(OH)₃Cl). These phases are metastable and transfer to Mn₃O₄ with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn₃O₄, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn₂O₃–MnO₂ buffer. So at 400C, dissolved Au (log m_Au) increases from –4. 40 in water to –1. 00 in 0. 1 m_HCl, and ones of Pt (log m_Pt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.     

Na-rich carbonate inclusions in perovskite and calzirtite from the Guli intrusive Ca-carbonatite,polar Siberia

Carbonate phases, some rich in Na₂O and comparatively rich in SrO and BaO, occur as inclusions in perovskite and calzirtite (Ca₂Zr₅Ti₂O₁₆) in the carbonatite of the Guli complex, Siberia. This is the first record of alkali carbonates, akin to nyerereite [Na₂Ca(CO₃)₂], in plutonic igneous rocks. The inclusion populations suggest that the parental magma of the complex was Ca-rich but developed Na-rich differentiates during the latest stages. This points to the dominant calcic carbonatites of the complex not being derivatives of alkali-rich parental carbonatites. These alkali-rich carbonate inclusions (and rare inclusions of djerfisherite) have been preserved due to the resistance of perovskite and calzirtite to processes of leaching, hydrothermal alteration and weathering.