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Maria Economou-Eliopoulos 《Ore Geology Reviews》1996,11(6):363-381
Compilation of some new data on ophiolites for Greece and Yugoslavia, and published data from previous studies, indicate that platinum-group element (PGE) and gold concentrations in chromite ores are generally low, ranging from less than 100 ppb to a few hundred ppb. However, samples from several ophiolite complexes exhibit an enrichment (of a few ppm) (a) only in Os, Ir and Ru,(b) only in Pt and/or Pd or (c) in all PGE. This enrichment (up to 10s ppm) is mainly related with chromitites hosted in supra-Moho dunites and dunites of the uppermost stratigraphic levels of the mantle sequence and it seems to be local, independent of the chromitite major element composition and the chromite potential of the ophiolite complexes. The contents of PGE combined with less chalcophile elements (Ni, Co, Cu), the ratios of incompatible/compatible elements, and PGE-patterns provide evidence for discrimination between chromitites derived from primitive magmas and those derived from partially fractionated magmas, although they have a similar major element composition. Thus, they can be used for a stratigraphic orientation in the mantle sequence, and therefore for exploration targets. Moreover, PGE data offer valuable information for the evaluation of the chromite potential in ophiolite complexes. The most promising ophiolites seem to be those which apart from the petrological and geochemical characteristics indicating extensive degree of partial melting in the mantle source contain only one chromite ore type (the other type being only in small proportion) of limited compositional variation, in both major elements and PGE, low ratios of , while PGE-enriched chromitites in the mantle sequence are only occasionally present. In contrast, ophiolites which contain both high-Cr and -Al chromitites, and where their chalcophile element data implies relatively extensive fractionation trend are not good exploration targets for chromite ores, although they are related with a SSZ environment. 相似文献
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Summary In the serpentinizedophiolitic rocks from Skyros island, two distinct assemblages of base metal sulphides (BMS) and platinum-group minerals (PGM) occur. The first (early) generation is associated with chromitites which are enriched in platinum-group elements (PGE). The highest values were recorded in samples from Achladones (Ru 1210, Ir 780, Os 630, Rh 228, Pt 208, Pd 22; all values in ppb). Mineral inclusions in chromite consist of Ni-Fe sulphides and Os-rich laurite, and crystallized at high sulphur fugacity (fS2) during chromite formation. The second (late) generation is closely associated with Au-rich, PGE-poor magnetite ores which host a complex assemblage of inclusions consisting mainly of graphite, Cu-Fe- and pure Cu sulphides, sperrylite and tetraauricupride. Their accompanying hydrous silicates are Cl-bearing. It is assumed that this mineral assemblage was deposited by hydrothermal processes during serpentinization.
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Minerale der Platingruppe und Tetraauricuprid in Ophiolithen der Insel Skyros, Griechenland
Zusammenfassung In den serpentinisierten Ophiolithen der Insel Skyros wurden zwei unterschiedliche Bildungsgenerationen von Sulfiden (BMS) und Platinmineralen (PGM) festgestellt. Die erste (frühere) Generation ist an Chromitite gebunden, die hohe Gehalte an Elementen der Platingruppe (PGE) aufweisen. Die höchsten PGE-Kontzentrationen wurden in den Proben der Lokalität Achladones gefunden (Ru 1210, Ir 780, Os 630, Rh 228, Pt 208, Pd 22; alle Gehalte in ppb). Die Einschlüsse in Chromit bestehen aus Ni-Fe Sulfiden und Os-reichem Laurit. Diese Minerale kristallisierten bei hoher Schwefelfugazität (fS2) während der Bildung der Chromite. Die zweite (spätere) Generation ist eng assoziiert mit Au-reichen und PGE-armen Magnetiten. Sie führen eine komplexe Einschluß-Paragenese bestehend aus Graphit, Cu-Fe- und reinen Cu Sulfiden sowie Sperrylith und Tetraauricuprid. Die begleitenden Hydrosilikate sind Cl-haltig. Die Bildung dieser Mineralparagenese wird durch hydrothermale Prozesse während der Serpentinisierung erklärt.
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3.
An integrated approach was performed on the soil,plant-crops and groundwater system at the Thiva basin,to evaluate the extent and intensity of the heavy metal contamination,the percentage of metals tra... 相似文献
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The Parnassos-Ghiona bauxite deposit in Greece of karst type is the 11th largest bauxite producer in the world. The mineralogical, major and trace-element contents and δ18O, δ12C, δ34S isotopic compositions of bauxite ores from this deposit and associated limestone provide valuable evidence for their origin and biogeochemical processes resulting in the beneficiation of low grade bauxite ores. The organic matter as thin coal layers, overlying the bauxite deposits, within limestone itself (negative δ12C isotopic values) and the negative δ34S values in sulfides within bauxite ores point to the existence of the appropriate circumstances for Fe bio-leaching and bio-mineralization. Furthermore, a consortium of microorganisms of varying morphological forms (filament-like and spherical to lenticular at an average size of 2 μm), either as fossils or presently living and producing enzymes, is a powerful factor to catalyze the redox reactions, expedite the rates of metal extraction and provide alternative pathways for metal leaching processes resulting in the beneficiation of bauxite ore. 相似文献
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Maria Economou-Eliopoulos Ifigenia Megremi Charalampos Vasilatos 《Chemie der Erde / Geochemistry》2011,(1):39-52
The effective influence of industry or ultramafic rocks by natural processes to soil, plants and groundwater contamination by chromium, which is often a subject of debate, was investigated for the case of the Assopos basin, Greece. The Neogene Assopos basin, is mainly composed by Tertiary and Quaternary sediments of more than 400 m thick and is characterized by brittle type deformation (fault zones, faults). Chromium in soil, ranging from 67 to 204 ppm, is mostly hosted in chromite, Fe-chromite, Cr-bearing goethite and silicates.Special attention was given to the plants, which are a major source of organic matter that serves as the driving force for Cr(VI) reduction. The increase of the Fe, Mn and Ni contents, with the increasing Cr content in the plant-roots, in particular at the external parts of roots and those of bulb-type plants, suggest reduction and immobilization of Cr(VI) and that redox reactions play a significant role to the translocation processes from root to shoot.Groundwater samples from the Assopos aquifer showed a wide spatial variability, ranging from <2 to 180 ppb Crtotal content [almost same to the Cr(VI)-values] despite their spatial association. The presence of Cr(VI)-contaminated groundwater at depths >200 m is attributed to a direct injection of Cr(VI)-rich industrial wastes at depth rather than that Cr(VI) is derived from the Assopos river or by the interaction between water and Cr-bearing rocks. The heterogeneous distribution of Cr in groundwater may be related with the intense neotectonic deformation, as is exemplified by several sharp tectonic contacts between sediment types, while the Cr content in soil is mostly depend on the transported chromite grains. 相似文献
7.
Evdokia E. Kampouroglou Maria Economou-Eliopoulos 《Central European Journal of Geosciences》2013,5(1):174-188
The first mineralogical and geochemical investigation of the travertine limestone, soil and corresponding plants associated with the Neogene basin of Varnavas, NE Attica, revealed a significant enrichment in the metalloid As. The total concentrations of As ranged from 61 to 210 ppm in limestone and 33 to 430 ppm in the associated soil demonstrating a wide variation of values. Calcite is a common authigenic mineral within travertine limestone, forming fine uniform micritic aggregates, having As and Mg concentrations lower than detection limits of EDS analysis. Clastic dominated minerals are quartz (both fine- and coarse-grained), muscovite, clinochlore, illite, pyrite, galena, arsenides, rutile, sphene, zircon, REE-minerals and albite. Goethite and Fe-Mn-oxides occur between calcite grains. The presence of fossilized micro organisms, resembling foraminifera, in travertine limestone combined with hydrous Fe-Mn-oxides, suggests a possible marine transgression during the evolution of the basin. The As content in plants ranges from 1.1 to 28 ppm As in shoots, and 0.8 to 114 ppm As in roots. The translocation factor, which is defined as the ratio of metal concentration in the shoots to the roots, is relatively low (average 0.33%) suggesting that the internal transport of metals from the roots to shoots was restricted. The bioaccumulation factor, which is defined as the ratio of metal concentration in the plants to that in soil, exhibits a wide range from relatively low (5.2–9.0% for As, Fe, Cr, Ni and Pb), much higher (56–67% for Cu and Zn) and exceptionally high (160% for Mo). A significant correlation between the translocation factors for Fe and As may confirm that Fe-Mn oxides/hydroxides represent the major sorbing agents for As in soils. The presented data, due to As contamination in travertine limestone, soil and plants, suggest a potential environmental risk not only for that part of Greece but in general for similar depositional environments. 相似文献
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Athinoula L. Petrou Maria Economou-Eliopoulos 《Geochimica et cosmochimica acta》2009,73(19):5635-5645
Small grains of Ru–Os–Ir sulfides or alloys that formed in the early stages of the crystallization of basaltic magmas occur as inclusions in chromitites from many ophiolite complexes, Ural/Alaskan-type and layered intrusions. The nature of platinum-group elements is debated, i.e., whether they originally occurred in a metallic state or bonded with sulfur or other ligands. The application of kinetics and suggestions regarding the mechanisms of PGE formation may contribute to a better understanding of the genetic processes for platinum-group mineral (PGM) formation. The aim of the present study is to investigate the type of mechanism (associative, dissociative or interchange) and the possibility of direct formation of PGM from the reaction of free metals with sulfur, defining also the structure of possible intermediate species.The literature on the grain sizes (r) of platinum-group minerals (PGM) and their formation temperatures (range between 700 and 1100 °C) reveals an Arrhenius temperature dependence. The activation energy was estimated to be 450 ± 45 kJ mol−1. Applying the Eyring equation to the same data, a linear relationship between 2.5ln(r) + ln(T) versus 1/T was obtained, leading to an estimation of the free energy of activation, ΔG≠ = 440 ± 43 kJ mol−1. The thermodynamic relation ΔG≠ = ΔH≠ − TΔS≠, used together with the relation ΔΗ≠ = Eact − RT leads to the calculation of ΔS≠ at various temperatures. The estimated entropy of activation at various temperatures being almost zero, we suggest an interchange mechanism for PGM formation.The possibility of PGM formation from the direct reaction of free metals with sulfur would be inconsistent with the estimated entropy of activation values (ΔS≠ 0) at various temperatures. In the cases of PGMs of known r, the formation temperatures can be estimated, and then the free energy of activation obtained, applying 2.5ln(r) + ln(T) versus 1/T (straight line). From that value, the entropy of activation can be calculated [ΔS≠ = −R + (Eact − ΔG≠)/T], and an interchange mechanism is proposed. Furthermore, applying the relation of 2.5ln(r) + ln(T) versus 1/T on PGM grains of known r and T, an interchange mechanism for their formation can be suggested if they fit the above line. 相似文献
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The Parnassos-Ghiona bauxite deposits of Greece are hosted within carbonate rocks and have been formed during different geological ages. The most economically important deposits occur in the B3 bauxite horizon, which is developed over long distance as a continuous layer of 1–10 m in thickness, within Cretaceous limestones. Due to intense tectonics, a significant (approximately 30 vol.%) bauxite ores along and near their contact with faults show a brittle deformation and change in the color from red to black-gray, in a distance of tens of meter. Commonly gray to whitish bauxites are aluminum-enriched (> 65 wt.% Al2O3) and iron depleted. 相似文献
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Chromitite occurrences in the Pindos ophiolite complex are located in elongated dunite bodies hosted in harzburgite of the mantle sequence, and show a compositional variation from high-Al to high-Cr type. Although the majority of the chromite ores is characterized by paucity in fluid inclusions, abundant fluid inclusions were found in chromite hosted by a coarse-grained pyroxenite dike at the Spanos Valley, Pindos complex. Chromite occurs in highly variable proportion in an orthopyroxene matrix or as inclusions in orthopyroxenes. Its composition is homogeneous and has an average Cr/(Cr+Al) ratio 0.73.The investigation of chromitites revealed the presence of primary and secondary fluid inclusions. The primary inclusions are of following types: Three-phase solid-liquid-gas, three-phase liquid-liquid-gas, two-phase liquid-gas and one-phase octahedron crystal-shaped. The secondary fluid inclusions are two-phase liquid-gas and mono-phase fluid inclusions.The presence of fluid inclusions in chromite aggregates hosted in orthopyroxenite dikes, in combination with the trace element contents in chromite concentrates and the mineralogical composition of the dikes may indicate that an aqueous phase separated from the magma. 相似文献