Lower crustal granulite xenoliths from the Pannonian Basin,Hungary, Part 2: Sr–Nd–Pb–Hf and O isotope evidence for formation of continental lower crust by tectonic emplacement of oceanic crust

Mafic granulite xenoliths from the lower crust of the Pannonian Basin are dominated by LREE-depleted bulk-rock compositions. Many of these have MORB-like ¹⁴³Nd/¹⁴⁴Nd but ⁸⁷Sr/⁸⁶Sr is elevated relative to most MORBs. Their '¹⁸O values cover a wide range from +3.8 to +9.5‰. A group of LREE-enriched mafic granulites have higher ⁸⁷Sr/⁸⁶Sr (0.704-0.708) and lower ¹⁴³Nd/¹⁴⁴Nd (0.5128-0.5124), with higher '¹⁸O values on average (+7.8 to +10.6‰) than the LREE-depleted granulites. The LREE-enriched granulites are, however, isotopically similar to newly discovered metasedimentary granulite xenoliths. A sublinear correlation in )Hf-)Nd isotope space has a shallower slope than the crust-mantle array, with the metasedimentary rocks forming the low )Hf end member; the radiogenic end is restricted to the LREE-depleted granulites and these overlap the field of MORB. Pb isotopes for the LREE-depleted samples are less radiogenic on average than those of the LREE-enriched and metasedimentary xenoliths, and metasedimentary granulites have consistently higher ²⁰⁸Pb/²⁰⁴Pb. The wide range in '¹⁸O over a restricted range in Nd and Sr isotope values, in combination with the predominance of LREE-depleted trace-element compositions, is consistent with an origin as a package of hydrothermally altered oceanic crust. The existence of '¹⁸O values lower than average MORB and/or mantle peridotite requires that at least some of these rocks were hydrothermally altered at high temperature, presumably in the oceanic lower crust. The low ¹⁴³Nd/¹⁴⁴Nd of the LREE-enriched mafic granulites cannot be explained by simple mixing between a LREE-depleted melt and an enriched component, represented by the recovered metasediments. Instead, we interpret these rocks as the metamorphic equivalent of the shallowest levels of the ocean crust where pillow basalts are intimately intercalated with oceanic sediments. A possible model is accretion of oceanic crustal slices during subduction and convergence, followed by high-grade metamorphism during the Alpine orogeny.     

Recent Precipitation Trends in Hungary in the Context of Larger Scale Climatic Changes

The time series of monthly precipitation totals from 14 Hungarian observing stations (1901–1998) were analysed to reveal the long term changes in precipitation characteristics occurred in the 20th century. A particular attention was given to the changes in the recent decades and their links with the larger scale climatic and circulation changes over Europe and the Atlantic.The statistical significancesof systematic changes are controlled by linear trend analysis and the Mann–Kendall test. The long term fluctuations are illustrated applying a 15-point Gaussian filter on the time series. The Standardised Precipitation Index is used to evaluate the changes in the drought event frequency. The relationships with larger scale changes are mostly discussed relying on contemporary papers, and the Grosswetterlagen Catalogue is used as well.The annual precipitation total decreased by 15–20% in Hungary during the 20th century. The decline is substantial in both halves of the century, but the precipitation sums in the transition seasons declined in the first 50 years, and the winter precipitation decreased in the latest decades. The precipitation total of the period November–February declined significantly in the last 50 years. In the same time the mean winter value of the North Atlantic Oscillation Index (NAOI) increased, the positions of the main pressure patterns over the Atlantic are shifted northeastward, and lot of other coherent changes detected in the winter climate of the European–Atlantic region. The mean summer precipitation total has hardly changed, but the frequency of summer drought events increased. There are some signs of a shift of the Hungarian summer climate towards a Mediterranean like climate.     

Feature Environmental geophysics: a site characterization tool for urban regeneration in the post-mining era

The closure and decay of industrial activity involving mining, chemical or light industrial operations has scarred the landscape of urban areas. The Government has major initiatives in urban regeneration to remediate these 'brown-field sites'.     

Timing of deformation in the Norseman-Wiluna Belt, Yilgarn Craton, Western Australia

Establishing relative and absolute time frameworks for the sedimentary, magmatic, tectonic and gold mineralisation events in the Norseman-Wiluna Belt of the Archean Yilgarn Craton of Western Australia, has long been the main aim of research efforts. Recently published constraints on the timing of sedimentation and absolute granite ages have emphasized the shortcomings of the established rationale used for interpreting the timing of deformation events. In this paper the assumptions underlying this rationale are scrutinized, and it is shown that they are the source of significant misinterpretations. A revised time chart for the deformation events of the belt is established. The first shortening phase to affect the belt, D₁, was preceded by an extensional event D_1e and accompanied by a change from volcanic-dominated to plutonic-dominated magmatism at approximately 2685–2675 Ma. Later extension (D_2e) controlled deposition of the ca 2655 Ma Kurrawang Sequence and was followed by D₂, a major shortening event, which folded this sequence. D₂ must therefore have started after 2655 Ma—at least 20 Ma later than previously thought and after the voluminous 2670–2655 Ma high-Ca granite intrusion. Younger transcurrent deformation, D₃–D₄, waned at around 2630 Ma, suggesting that the crustal shortening deformation cycle D₂–D₄ lasted approximately 20–30 Ma, contemporaneous with low-volume 2650–2630 Ma low-Ca granites and alkaline intrusions. Time constraints on gold deposits suggest a late mineralisation event between 2640–2630 Ma. Thus, D₂–D₄ deformation cycle and late felsic magmatism define a 20–30 Ma long tectonothermal event, which culminated with gold mineralisation. The finding that D₂ folding took place after voluminous high-Ca granite intrusion led to research into the role of competent bodies during folding by means of numerical models. Results suggest that buoyancy-driven doming of pre-tectonic competent bodies trigger growth of antiforms, whereas non-buoyant, competent granite bodies trigger growth of synforms. The conspicuous presence of pre-folding granites in the cores of anticlines may be a result from active buoyancy doming during folding.     

Controls on Fe reduction and mineral formation by a subsurface bacterium

The reductive dissolution of FeIII (hydr)oxides by dissimilatory iron-reducing bacteria (DIRB) could have a large impact on sediment genesis and Fe transport. If DIRB are able to reduce FeIII in minerals of high structural order to carry out anaerobic respiration, their range could encompass virtually every O₂-free environment containing FeIII and adequate conditions for cell growth. Previous studies have established that Shewanella putrefaciens CN32, a known DIRB, will reduce crystalline Fe oxides when initially grown at high densities in a nutrient-rich broth, conditions that poorly model the environments where CN32 is found. By contrast, we grew CN32 by batch culture solely in a minimal growth medium. The stringent conditions imposed by the growth method better represent the conditions that cells are likely to encounter in their natural habitat. Furthermore, the expression of reductases necessary to carry out dissimilatory Fe reduction depends on the method of growth. It was found that under anaerobic conditions CN32 reduced hydrous ferric oxide (HFO), a poorly crystalline FeIII mineral, and did not reduce suspensions containing 4 mM FeIII in the form of poorly ordered nanometer-sized goethite (α-FeOOH), well-ordered micron-sized goethite, or nanometer-sized hematite (α-Fe₂O₃) crystallites. Transmission electron microscopy (TEM) showed that all minerals but the micron-sized goethite attached extensively to the bacteria and appeared to penetrate the outer cellular membrane. In the treatment with HFO, new FeII and FeIII minerals formed during reduction of HFO-Fe in culture medium containing 4.0 mmol/L P_i (soluble inorganic P), as observed by TEM with energy-dispersive X-ray spectroscopy, selected area electron diffraction, and X-ray diffraction. The minerals included magnetite (Fe₃O₄), goethite, green rust, and vivianite [Fe₃(PO₄)₂ · 8H₂O]. Vivianite appeared to be the stable end product and the mean coherence length was influenced by the rate of FeIII reduction. When P_i was 0.4 mol/L under otherwise identical conditions, goethite was the only mineral observed to form, and less Fe²⁺ was produced overall. Hence, the ability of DIRB to reduce Fe (hydr)oxides may be limited when the bacteria are grown under nutrient-limited conditions, and the minerals that result depend on the vigor of FeIII reduction.     

Modelling nitrogen and oxygen isotope fractionation during denitrification in a lacustrine redox-transition zone

The stable isotope composition (δ¹⁵N and δ¹⁸O) of nitrate was measured during Summer 1999 in the anaerobic hypolimnion of eutrophic Lake Lugano (Switzerland). Denitrification was demonstrated by a progressive nitrate depletion coupled to increasing δ¹⁵N and δ¹⁸O values for residual nitrate. Maximum δ¹⁵N and δ¹⁸O values amounted to 27.2 and 15.7‰, respectively.¹⁵N and ¹⁸O enrichment factors for denitrification (ε) were estimated using a closed-system model and a dynamic diffusion-reaction model. Using the Rayleigh equation (closed-system approach), we obtained ε values of −11.2 and −6.6‰ for nitrogen and oxygen, respectively. The average ε values derived using the diffusion-reaction model were determined to be −20.7 ± 3.8 for nitrogen and −11.0 ± 1.7 for oxygen. Both N and O isotope fractionation appeared to be lower when denitrification rates where high, possibly in association with high organic carbon availability. In addition, variations in the isotope effects may be attributed to the variable importance of sedimentary denitrification having only a small isotope effect on the water column. The combined measurement of N and O isotope ratios in nitrate revealed that coupled nitrification-denitrification in the open-water was of minor importance. This is the first study of nitrogen and oxygen isotope effects associated with microbial denitrification in a natural lake. Moreover, this study confirms the high potential of δ¹⁸O of nitrate as a valuable biogeochemical tracer in aquatic systems, complementing nitrate δ¹⁵N.     

Intercomparison of Stratospheric Chemistry Models under Polar Vortex Conditions

Several stratospheric chemistry modules from box, 2-D or 3-D models, have been intercompared. The intercomparison was focused on the ozone loss and associated reactive species under the conditions found in the cold, wintertime Arctic and Antarctic vortices. Comparisons of both gas phase and heterogeneous chemistry modules show excellent agreement between the models under constrained conditions for photolysis and the microphysics of polar stratospheric clouds. While the mean integral ozone loss ranges from 4–80% for different 30–50 days long air parcel trajectories, the mean scatter of model results around these values is only about ±1.5%. In a case study, where the models employed their standard photolysis and microphysical schemes, the variation around the mean percentage ozone loss increases to about ±7%. This increased scatter of model results is mainly due to the different treatment of the PSC microphysics and heterogeneous chemistry in the models, whereby the most unrealistic assumptions about PSC processes consequently lead to the least representative ozone chemistry. Furthermore, for this case study the model results for the ozone mixing ratios at different altitudes were compared with a measured ozone profile to investigate the extent to which models reproduce the stratospheric ozone losses. It was found that mainly in the height range of strong ozone depletion all models underestimate the ozone loss by about a factor of two. This finding corroborates earlier studies and implies a general deficiency in our understanding of the stratospheric ozone loss chemistry rather than a specific problem related to a particular model simulation.