Enrichment processes at the base of the Archean lithospheric mantle: observations from trace element characteristics of pyropic garnet inclusions in diamonds

Trace element concentrations of peridotitic garnet inclusions in diamonds from two Chinese kimberlite pipes were determined using the ion microprobe. Garnet xenocrysts from the same two kimberlite pipes were also analyzed for comparison. In contrast to their extremely refractory major element compositions, all harzburgitic garnets showed enrichment in light rare earth elements (REE) relative to chondrite, resulting in sinuous REE patterns. Both normal and sinuous REE patterns were observed from the lherzolitic garnets. Concentrations of REE in garnets changed significantly from diamond to diamond and no specific correlations were observed with their major element compositions. Analyses of randomly selected two to three points within every grain of a large number of garnet inclusions by the ion microprobe demonstrated that there was no evident compositional heterogeneity, and multiple grains of one phase from a single diamond host also exhibit very similar compositions. This implies that the trace element heterogeneity within one grain or among multiple inclusions from the same diamond host, as reported from Siberian diamonds, is not a common feature for these Chinese diamonds. Concentrations of Na, Ti, and Zr tend to decrease when garnets become more refractory, but variations of Sr and Li are more complex. Compositions rich in light REE and relatively poor in high field strength elements (HFSE) of the harzburgitic garnet inclusions in diamonds are generally consistent with metasomatism by carbonatite melts. The trace element features observed from the garnet inclusions in Chinese diamonds may be caused by carbonatite melt infiltration and partial melt extraction. Spatial and temporal gradients in melt/rock ratio and temperature are the main reasons for the large variations of REE patterns and other trace element concentrations. Received: 27 April 1999 / Accepted: 1 March 2000     

Biogeochemistry of trace metals (Mn, Sr, Rb, Ba, Cu, Zn, Pb and Cd) in a river-wetland-lake system (Balaton Region, Hungary)

Mn, Sr, Ba, Rb, Cu, Zn, Pb and Cd concentrations have been measured seasonally in the water and deposited sediments of the system comprising: Zala river (main input) — Lakes Kis-Balaton 1 and 2 (small artificial lakes created in a former bay of Lake Balaton) — Keszthely bay (hypertrophic part of Lake Balaton). The concentrations of the trace elements together with pH, alkalinity, dissolved cations (Ca²⁺, Mg²⁺, Na⁺, and K⁺), dissolved inorganic ligands (Cl^–, SO₄ ^2–), particulate Al, Ca, inorganic and organic carbon are used to assess the contamination of the study area and biogeochemical processes controlling trace element concentrations. Thermodynamic speciation calculations have also been utilized to enhance our understanding of the system. In the sediments Rb, Ba, Cu and Zn concentrations were mainly controlled by the abundance of the aluminosilicate fraction. Strontium was mainly associated with the calcium carbonate fraction. The aluminosilicate fraction constitutes a major sink for Mn and Cd but the concentration of these elements are also strongly related to calcite precipitation. The main processes that control the dissolved distribution of trace elements in the Balaton system were: solid phase formation (carbonate) for Mn; coprecipitation with calcite for Sr, Ba, Rb and possibly Mn and Cd; adsorption/desorption processes (pH dependent) for Zn and Pb; solubilization of Mn and precipitation of Cd and Cu in reed covered wetland areas where anoxic conditions were probably existing during the warm season. A preliminary budget of atmospheric and river input to Lake Balaton has also been outlined. Although Lake Balaton, is subjected to anthropogenic inputs mainly from agricultural and domestic activities, their impact on trace element concentrations in the Balaton system is very limited due to the efficiency of removal processes (i.e. adsorption and co-precipitation) and to high sedimentation rates and strong sediment re-suspension. Anthropogenic inputs are only detected for Pb.     

Estimation of the dispersion of an accidental release of radionuclides and toxic materials based on weather type classification

We investigate the influence of the regional-scale weather types on the atmospheric dispersion processes of the air pollutants originated from point sources. Hypothetical accidents were simulated with two different dispersion models. During a year’s test period, the 6-h emission of a radionuclide from the Paks Nuclear Power Plant (Paks NPP, Hungary) was assumed every day and the transport and deposition of the radionuclide was simulated by the Eulerian TREX dispersion model over the Central European region. In addition, the ALOHA Gaussian air dispersion model was also used for the local environment of the Paks NPP to simulate hypothetical hourly releases of ammonia during a 10-year period. During both types of model simulations, the dispersion of the plume for each time was analysed and tested with consideration of 13 circulation types corresponding to daily weather patterns over the Carpathian Basin. There are significant correlations between circulation types and plume directions and structures both in local and regional scales. The daily circulation pattern can be easily obtained from weather analyses; the expected size and direction of polluted area after an accidental release can be quickly estimated even before an accident occurs. However, this fast method cannot replace or neglect dispersion model simulations. It gives a ‘first guess’ and a fast estimation on the direction of the plume and can provide sufficient information for decision-making strategies.     

Potential nitrogen fixation changes under different land uses as influenced by seasons and biochar amendments

Soil nutrient dynamics, potential biological nitrogen fixation (BNF) changes, and their relations were studied using four land use types. Further, we investigated BNF changes in the presence of biochar in soils. Soil samples were collected from arable, vineyard, grassland, and forest soils during four seasons, and analyzed for abiotic contents of total nitrogen, NH₄⁺-N, NO₃^?-N, ammonium lactate (AL)-soluble K₂O, P₂O₅, and soil organic carbon (SOC) concentrations. Potential N₂ fixation was measured as ethylene (C₂H₄) production from acetylene (C₂H₂) reduction (ARA). The study focused on the changes in ARA when different types of biochars (T600, T650, and T700) were applied to soil samples in different amounts (0, 0.5, 2.5, and 5.0% wt wt^?1) under laboratory conditions. We found strong correlations between soil chemical parameters and ARA values, especially in the case of soil pH, total N, SOC, and P₂O₅ contents. In the case of arable soil, the ARA measurements were up to 227 times higher compared to grassland and forest samples. Biochar application affected N₂-fixing microbial responses among land use types, most notably decreases in arable lands and forest soils. We found that a high amount of biochar added to the soils can greatly suppress N₂-fixing activities. Our results highlight the strong relationship between soil nutrient changes and the intensity of anthropogenic influence.     

GGR Biennial Critical Review: Analytical Developments Since 2010

Advances in the chemical and isotopic characterisation of geological and environmental materials can often be ascribed to technological improvements in analytical hardware. Equally, the creation of novel methods of data acquisition and interpretation, including access to better reference materials, can also be crucial components enabling important breakthroughs. This biennial review highlights key advances in either instrumentation or data acquisition and treatment, which have appeared since January 2010. This review is based on the assessments by scientists prominent in each of the given analytical fields; it is not intended as an exhaustive summary, but rather provides insight from experts of the most significant advances and trends in their given field of expertise. In contrast to earlier reviews, this presentation has been formulated into a unified work, providing a single source covering a broad spectrum of geoanalytical techniques. Additionally, some themes that were not previously emphasised, in particular thermal ionisation mass spectrometry, accelerator‐based methods and vibrational spectroscopy, are also presented in detail.     

Retrograde alterations of phyllosilicates in low-grade metapelite: a case study from the Szendr? Paleozoic, NE-Hungary

Frequently, at temperatures lower than the metamorphic peak conditions, slates undergo mineral transformations, usually mediated by fluids. We have studied core material of an epizonal slate series (Szendr? Mountains, NE-Hungary) to reconstruct the post-metamorphic lower-T hydrothermal alterations using petrographic, X-ray diffraction, electron microprobe methods, and transmission electron microscopy. The borehole crosscuts an upper part of the ca. 600?C800?m Lower-Carboniferous flysch-like Szendr? Phyllite Formation. The samples were metamorphosed reaching epizonal conditions with a mineral assemblage characterized by quartz, muscovite, chlorite and albite. Even in the freshest samples, break-up and loosening of the regional metamorphic structure was observed, with cracks parallel to or crossing the cleavage. In the upper part, chlorite and albite are almost absent, while the presence of paragonite, mixed Na?CK mica, and mixed-layered minerals with smectitic component are characteristic. Goethite, halloysite, and subordinate kaolinite are present in the most altered sample (13.0?m in the profile) which may indicate the position of the fissures in which the circulation of the post-metamorphic fluids was the most intense. Muscovite is the only mica from the lower part of the profile and chlorite becomes a significant constituent, whereas paragonite, halloysite, and kaolinite are missing. Discrete smectite is present in all the samples in spite of being incompatible with the prograde evolution of the sequence. The interleaved smectite layers in chlorite and muscovite/chlorite mixed-layers show at the lattice level textural characteristics indicative of a later alteration process. After the metamorphic peak at epizonal conditions, the introduction of hot fluids through the fractures gave rise to the crystallization of Na?CK white micas and muscovite/chlorite under anchizonal conditions. In a final stage of the hydrothermal process, the cooling of the circulating fluids favored the formation of halloysite and kaolinite in the areas near to the fissures, smectites in the samples far away from the fractures, and locally, goethite. The Fe₂O₃ content increasing upwards indicates oxidizing conditions in the late stage of hydrothermal activity and/or eventually, an influence of a younger near-surface weathering.     

A model for the layered upper mantle

Numerical modeling of mantle convection by Liu (1994, Science, 264: 1904–1907) favors a two-layer convection, if the results are reinterpreted for the correct phase relations in (Mg,Fe)₂SiO₄. The resulting chemical isolation of the upper and lower mantle suggests a highly differentiated and layered upper mantle to account for the discrepancy between the observed compositions of mantle xenoliths and the cosmic abundances of elements. It is shown that a layered upper mantle with a hidden reservoir can have a structure consistent with the observed seismic velocity profiles and an average bulk composition corresponding to the cosmic abundances. The evolution of the upper mantle and the origin of komatiites are discussed in the context of the proposed model.