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51.
52.
Tibor Gasparik 《Contributions to Mineralogy and Petrology》1984,87(1):87-97
In the system CaO-MgO-Al2O3-SiO2 (CMAS), equilibrium alumina contents of orthopyroxene and clinopyroxene, both coexisting with spinel + forsterite or spinel + anorthite, have been reversed in 16 runs at 1,300–1,400°C and 10.2–20.8 kbar, using PbO flux. The present data and the data of Perkins and Newton (1980) have been modeled using the Redlich-Kister equation. The resulting model satisfies most of the reversed data in the CMAS system, agrees very well with thermochemical measurements, and is consistent with the model for the enstatite-diopside join of Lindsley et al. (1981) and with the system MgO-Al2O3-SiO2 of Gasparik and Newton (1984). The present data, however, do not confirm the negative slopes of Al-isopleths in the spinel lherzolite field suggested by Dixon and Presnall (1980). The new model has been used to calculate a graphical two-pyroxene thermobarometer applicable to natural two-pyroxene assemblages closely approaching in composition the CMAS system. 相似文献
53.
Tibor Gasparik 《Geochimica et cosmochimica acta》1984,48(12):2537-2545
Subsolidus phase relations in the system CaO-Al2O3-SiO2 (CAS) were experimentally determined with tight reversals of several univariant curves and with 14 equilibration experiments containing the assemblage pyroxene + anorthite, where pyroxene is a binary solid solution of Ca-Tschermak (CaTs-CaAl2SiO6) and Ca-Eskola (CaEs-Ca0.5AlSi2O6) endmembers.Reversals were obtained on the following reactions (bar, °C): 3An = Gr + 2Ky + Q (P = 22T ? 700), 3An + Cor = Gr + 3Ky (P = 21.8T ? 950), 3CaTs= Gr + 2Cor(P = 55T ? 53900), and 6CaTs(1 ? x)CaEsx = 2(1 ? 2x)Gr + 4(1 ? 2x)Cor + 9xAn. Observed slopes indicate 9.8 J/mol · K of Al-Si disorder in Ca-Tschermak pyroxene and 5.3 J/mol·K of Al-Si disorder in anorthite, at 1300°C. It is suggested that Al-Si disorder in anorthite increases by 1.9 J/mol · K from 700°C to 1300°C.Compositions of CaTs-CaEs pyroxene in equilibrium with anorthite and PbO-rich liquid were experimentally determined at 1400–1430°C and 22.7–30.8 kbar. Microprobe measurements gave compositions which are consistent with an ideal pyroxene solution and the following parameters for the reaction 3An = 2CaTs + 2CaEs (J, bar, K): 2RTln(XCaTs · XCaEs) + 60200 + 86.4T ? (5.06 + 13 × 10?7P)P = 0, resulting in ΔH0j = ?39.8 kJ/mol and S0 = 461.8 J/mol · K for the Ca-Eskola endmember at 1300°C. The obtained properties of the Ca-Eskola component are necessary for thermobarometry based on pyroxene bearing assemblages containing plagioclase, quartz, or kyanite. 相似文献
54.
The shredder guild plays an outstanding role in the functioning of headwater stream ecosystems by processing allochthonous leaf litter. Traditionally, the abiotic habitat template is regarded as the major determinant of its organization, and only a limited number of studies support the importance of biotic interactions. The aim of the present study was to examine whether competition plays a significant role in organizing the shredder guild of caddisflies in a riffle. Null-model based co-occurrence, co-existence and guild variation analyses were used in the study of guild organization. In addition, the traditional variance to mean ratio was applied for measuring the intraspecific aggregation of guild members. The non-significant metric values of co-occurrence and co-existence analyses predicted that competition was of limited importance in structuring the spatial organization of the shredder guild. The observed aggregated spatial distribution of species, suggests that besides stochastic events, deterministic forces should also contribute to the organization of the shredder guild of caddisflies. 相似文献
55.
56.
We propose guidelines for the reporting of in situ cosmogenic nuclide data for exposure age and erosion rate determinations. This is motivated by the need to maintain the utility of such data in the future, and to delineate best scientific practice. These guidelines will allow published exposure ages and erosion rates to be recalculated with confidence by others in the future, if, as is likely, procedures to calculate cosmogenic nuclide production rates are modified in the meantime. 相似文献
57.
Wuyi Wang Shigeho Sueno Eiichi Takahashi Hisayoshi Yurimoto Tibor Gasparik 《Contributions to Mineralogy and Petrology》2000,139(6):720-733
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 相似文献
58.
Françoise Elbaz-Poulichet Attila Nagy Tibor Cserny Piroska Pomogyi 《Aquatic Geochemistry》1996,2(4):379-402
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. 相似文献
59.
Péter árkai Isabel Abad Fernando Nieto Tibor Németh Péter Horváth Viktória K. Kis Katalin Judik Juan Jiménez-Millán 《Swiss Journal of Geoscience》2012,105(2):263-282
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. 相似文献
60.
Michael Wiedenbeck Roxana Bugoi M. John M. Duke Tibor Dunai Jacinta Enzweiler Mary Horan Klaus Peter Jochum Kathryn Linge Jan Košler Silke Merchel Luiz F.G. Morales Lutz Nasdala Roland Stalder Paul Sylvester Ulrike Weis Arnaud Zoubir 《Geostandards and Geoanalytical Research》2012,36(4):337-398
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. 相似文献