甘肃南梁—华池地区三叠系延长组长三段储层物源探讨   总被引：1，自引：0，他引：1  

王瑞飞  陈明强  孙卫 《地层学杂志》2008,32(2):194-200

利用稀土元素和微量元素,分析鄂尔多斯盆地南部南梁—华池地区上三叠统延长组长三段储层母岩类型和物源方向,研究表明盆地南部南梁—华池地区延长组砂岩和泥岩的稀土元素地球化学特征、REE分配模式及微量元素蜘蛛图解相同,与盆地东北缘太古代、元古代变质岩相似,但不相同;与盆地西南缘的水河地区延长组相似且不同,说明研究区与盆地东北缘和西南缘均有较好的亲缘关系。结合轻、重矿物组合和盆地周缘古陆岩矿特征,证实了研究区物源为两个主物源的混合区。  相似文献   

Investigation of datolite (CaB[SiO₄/(OH)]) from basalts in the Northern Apennines ophiolites (Italy): Genetic implications     

F. Zaccarini  S. Morales-Ruano  M. Scacchetti  K. Heide 《Chemie der Erde / Geochemistry》2008,68(3):265-277

Datolite, ideally CaB[(OH/SiO₄)], from hydrothermal veins crosscutting pillow basalt in 10 different localities of the Northern Apennine ophiolites was investigated with regard to mineral chemistry and fluid inclusion microthermometry. Bulk analyses of datolite crystals show REE contents below chondritic, except for La and Ce. With respect to host rock, datolite is occasionally enriched in La, Rb, Cs, Be, and shows relatively high contents of chalcophile elements (Cu, Zn, Pb, Ni) when occurring in contact with sulfide-mineralized basalt. Volatiles escaped during the decomposition in the temperature range 600 and 700 °C. The main component is water. The temperature maximum of water release is different and frequently with a shoulder or a second maximum. Together with water, sulfur species as H₂S and SO₂ and traces of boron species escaped. The CO₂ release by the decomposition especially of datolite from Castellaro and Cinghi has a maximum in the range of 500-580 °C and is different from the decomposition of calcite. Together with CO₂ a boron species escaped. Chlorine does not detect. Two-phase (L+V) fluid inclusions texturally identifiable as primary and secondary were observed, yielding average homogenization-temperatures of 236 and 173 °C, respectively. Fluid inclusion cooling data yield calculated salinity in the range of 10-16 wt% NaCl equivalents, thus relatively higher compared with seawater. The results are compatible with those reported for fluids formed under diagenetic conditions, but differ from those observed in seafloor hydrothermal systems and/or emanating from magmas. Distribution of trace elements between datolite and host basalt indicates enrichment with respect to the host rock limited to a few elements such as La, Rb, Cs, Be, Ni, Cu, Zn and Pb. The lithophile elements can be hosted in the datolite lattice, whereas the chalcophile metals and Ni are probably carried in sub-microscopic inclusions.  相似文献   

Spurenelementgehalt der Saale – ein Vergleich der Analysenergebnisse aus den Jahren 1950 und 1996     

G. Proft  W. Schrn 《Chemie der Erde / Geochemistry》2008,68(2):221-233

Thirty four elements dissolved in water and 33 elements bound in particulate matter were analysed in the small river Saale (Thuringia, Germany, MQ=23 m³/s) in 1996 and the results were compared with those obtained in 1950 (44 elements). Monthly sampling was used to eliminate fluctuations caused by seasons and weather. Comparison of the element contents of a river over a 40-year-time span provides interesting insight into the anthropogenic change in the catchment area of the river with regard to „global change”.Without taking into consideration systematic errors, the analysed elements can be divided into three groups:

(a) Elements whose average annual analytical values in 1996 were lower by >50% than those in 1950: Al, As, Ba, Fe, Pb, Zn (in solution), and As, B, Cr, Li, Mn, Pb, Se, Sn, U (suspended).

(b) Elements whose average annual analytical values in 1996 are in the range of those in 1950, i.e., are within 50–150%: Ca, Co, Cr, F, K, Li, Mn, Na, Si, Sr, Ti, U (in solution), and Hg, Cr, Cu, Sc, Sr, Ti, Zn (suspended).

(c) Elements whose average annual analytical values in 1996 were higher by >150% than those in 1950: B, Cd, Mg, Ni, Rb, Sc (in solution), and Ba, Ni, P, Zr (suspended).

The increases in the element concentrations are not only caused by wastewater. Acid rain and fertilizer affect the pH and the electrolyte status of soils and cause mobilization of elements. This can be a reason for the increase in the alkalies and alkaline earth. For most elements are higher and lower values were found in 1996 and are only partly caused by systematic errors in the methods used in 1950. Taking into consideration of the natural fluctuations some element values 1996 equal or are lower (Tabelle 10 and 12). Because of the 100–200% RSD (12 samples per year), it is almost impossible to decide whether the deviations are due to analytical errors or to natural causes. The bound part of the elements is considered to be the suspended portion (seston=particulate matter) and, for one and the same element the suspended portion is equal or higher than the portion in solution. In the case of natural plant stock in the catchment area, the erosion is small. The increase in farming caused a higher soil erosion in the river. Storm precipitation causes short-term (1–2 h) peaks in the suspended load with values 2–3 orders of magnitude higher. In the case of monthly sampling, such peaks are unlikely to be detected. This produces values of suspended loads that tend to be too small. Increases of the bounded elements together with the elements in solution cause increases of eutrophication in the ocean.The contents of elements transported in solution and in particulate form in the river Saale are not equal to the element contents of the upper earth crust. Weathering and the fluviatil element transport cause a fractionation of the thallassophile (enriched in ocean) and therraphile elements (enriched in continents). Thallassophile elements are Mg, Ca, Sr, B, As, U, Sn, Cd, Zn, Se (transported in solution) and U, Cr, Li, B, Ba, Se, Mn, Cu, P, Sn, Cd, Rb, Pb, S and Zn (transported in seston) and therraphile elements are Cs, Co, Sc, Ni, Ti, Fe, Al, and K. As a result a fractionation in thallassophile and therraphile elements results and influences the geochemical cycles like magmatic differentiations.  相似文献   

Upper crustal abundances of trace elements: A revision and update   总被引：7，自引：0，他引：7  

Zhaochu Hu  Shan Gao   《Chemical Geology》2008,253(3-4):205-221

We report new estimates of abundances of rarely analyzed elements (As, B, Be, Bi, Cd, Ge, In, Mo, Sb, Sn, Te, Tl, W) in the upper continental crust based on precise ICP-MS analyses of well-characterized upper crustal samples (shales, pelites, loess, graywackes, granitoids and their composites) from Australia, China, Europe, New Zealand and North American. Obtaining a better understanding of the upper crustal abundance and associated uncertainties of these elements is important in placing better constraints on bulk crust composition and, from that, whole Earth models of element cycling and crust generation. We also present revised abundance estimates of some more commonly analyzed trace elements (Li, Cr, Ni, and Tm) that vary by > 20% compared to previous estimates. The new estimates are mainly based on significant (r² > 0.6) inter-element correlations observed in clastic sediments and sedimentary rocks, which yield upper continental crust elemental ratios that are used in conjunction with well-determined abundances for certain key elements to place constraints on the concentrations of the rarely analyzed elements. Using the well-established upper crustal abundances of La (31 ppm), Th (10.5 ppm), Al₂O₃ (15.40%), K₂O (2.80%) and Fe₂O₃ (5.92%), these ratios lead to revised upper crustal abundances of B = 47 ppm, Bi = 0.23 ppm, Cr = 73 ppm, Li = 41 ppm, Ni = 34 ppm, Sb = 0.075, Te = 0.027 ppm, Tl = 0.53 ppm and W = 1.4 ppm. No significant correlations exist between Mo and Cd and other elements in the clastic sediments and sedimentary rocks, probably due to their enrichment in organic carbon. We thus calculate abundances of these elements by assuming the upper continental crust consists of 65% granitoid rocks plus 35% clastic sedimentary rocks. The validity of this approach is supported by the similarity of SiO₂, Al₂O₃, La and Th abundances calculated in this way with their upper crustal abundances given in Rudnick and Gao [Rudnick, R., Gao, S., 2003. Composition of the continental crust. In: Rudnick, R.L. (Ed.), The Crust. In: Holland, H.D., Turekian, K.K. (Eds.), Treatise on Geochemistry, vol. 3. Elsevier–Pergamon, Oxford, pp. 1–64.]. The upper crustal abundances thus obtained are Mo = 0.6 ppm and Cd = 0.06 ppm. Our data also suggest a  20% increase of the Tm, Yb and Lu abundances reported in Rudnick and Gao [Rudnick, R., Gao, S., 2003. Composition of the continental crust. In: Rudnick, R.L. (Ed.), The Crust. In: Holland, H.D., Turekian, K.K. (Eds.), Treatise on Geochemistry, vol. 3. Elsevier–Pergamon, Oxford, pp. 1–64.].  相似文献   

Age and duration of ultrahigh-temperature metamorphism in the Anápolis–Itauçu Complex, Southern Brasília Belt, central Brazil – constraints from U–Pb geochronology, mineral rare earth element chemistry and trace-element thermometry     

J. A. BALDWIN  M. BROWN 《Journal of Metamorphic Geology》2008,26(2):213-233

Integrated petrographic and chemical analysis of zircon, garnet and rutile from ultrahigh‐temperature (UHT) granulites in the Anápolis–Itauçu Complex, Brazil, is used to constrain the significance of zircon ID‐TIMS U–Pb geochronological data. Chondrite‐normalized rare earth element (REE) profiles of zircon cores have positive‐sloping heavy‐REE patterns, commonly inferred to be magmatic, whereas unambiguous metamorphic grains and overgrowths have flat to slightly negatively sloping heavy‐REE patterns. However, in one sample, a core of zircon interpreted as having formed prior to garnet crystallization and a metamorphic zircon formed within microstructures involving garnet breakdown both display elevated heavy‐REE (and Y) with positive‐sloping patterns. D_REE(zrc/grt) partition coefficients suggest an approximation to equilibrium between zircon and garnet cores, although progressive enrichment in heavy REE towards garnet rims occurs in two of the samples investigated. Titanium‐in‐zircon thermometry indicates zircon growth during both the prograde and post‐peak evolution, but not at peak temperatures of the UHT metamorphism. By contrast, zirconium‐in‐rutile thermometry of inclusions armoured by garnet records crystallization temperatures, based on the upper end of the interquartile range of the data, of ～890 to 870 °C and maximum temperature around 980 °C, indicating prograde and retrograde growth close to and after peak conditions. Rutile located in retrograde microstructures records crystallization temperatures of 850 to 820 °C. Rutile intergrown with ilmenite and included within orthopyroxene, which is associated with exsolved zircon, records temperatures ～760 °C, consistent with Ti‐in‐zircon crystallization temperatures. ID‐TIMS U–Pb geochronological data from two of the four samples investigated define upper intercept ages of 641.3 ± 8.4 Ma (MSWD 0.91) and 638.8 ± 2.5 Ma (MSWD 1.03) that correlate with periods of zircon growth along the prograde segment of the P–T path. Individual zircon U–Pb dates retrieved from all samples range from 649 to 634 Ma, indicating a maximum duration of c. 15 Myr for the UHT event. This period is interpreted as recording modest thickening of hot backarc lithosphere located behind the Arenópolis Arc at the edge of the São Francisco Craton consequent upon terminal collision of the Parána Block with the arc during the amalgamation of West Gondwana.  相似文献   

A discrete element model for kaolinite aggregate formation during sedimentation   总被引：1，自引：0，他引：1  

Ning Lu  Matthew T. Anderson  William J. Likos  Graham W. Mustoe 《国际地质力学数值与分析法杂志》2008,32(8):965-980

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Geochemical behavior of rare earth elements in hydrothermally altered rocks of the Kuroko mining area,Japan     

N. Shikazono  Y. Ogawa  M. Utada  D. Ishiyama  T. Mizuta  N. Ishikawa  Y. Kubota 《Journal of Geochemical Exploration》2008

In this study we analyzed the chemical composition of hydrothermally altered dacite and basalt from the Kuroko mining area, northeastern Honshu, Japan, by REE (rare earth element). Features of rare earth element analyses include: (1) altered footwall dacite exhibits a negative Eu anomaly compared with fresh dacite, suggesting preferential removal of Eu²⁺ from the altered dacite via hydrothermal solutions, (2) altered hangingwall dacite and basalt and dacite and basalt adjacent to ore deposits exhibit positive Eu anomalies compared with fresh dacite and basalt, suggesting addition of Eu²⁺ from hydrothermal solutions, (3) LREE ratio (∑LREE/∑REE) from altered dacite of chlorite–sericite zone and K-feldspar zone show a negative relationship with δ¹⁸O, and La/Sm ratios show a positive correlation with the K₂O index. These trends indicate the addition of light rare earth elements such as La to the altered dacite from hydrothermal solution and/or leaching of heavy rare earth elements such as Sm and Yb, (4) Principal component analysis (PCA) indicates that light rare earth elements enrichment is related to the formation of sericite zone near the Kuroko deposits but not to the formations of chlorite and K-feldspar zones, and (5) The correlations among REE features (LREE ratio, MREE ratio, HREE ratio, Eu/Eu?), δ¹⁸O and K₂O index are not found for montmorillonite zone, mixed layer clay mineral zone and mordenite zone. Therefore, it is inferred that sericite, chlorite and K-feldspar alterations are related to the Kuroko and vein-type mineralization, but montmorillonite and mordenite alterations are not related to the mineralizations, and probably they formed at the post-mineralization stage.  相似文献   

The Double Solid Reactant Method for modeling the release of trace elements from dissolving solid phases: I. Outline and limitations     

Marina Accornero  Luigi Marini 《Environmental Geology》2008,55(8):1627-1635

A Double Solid Reactant Method was elaborated from a suggestion of Marini (Geological sequestration of carbon dioxide: Thermodynamics, kinetics, and reaction path modeling. Developments in Geochemistry, Elsevier, Amsterdam, 2007) to simulate the release of trace elements during the progressive dissolution of solid phases. The method is based on the definition, for each dissolving solid, of both an entity whose thermodynamic and kinetic properties are known (either a pure mineral or a solid mixture) and a special reactant, that is, a material of known stoichiometry and unknown thermodynamic and kinetic properties. The special reactant is utilised to take into account the concentrations of trace elements in the dissolving solid phase. In this communication, the influence of several trace elements on the ΔG _f ^o, ΔG _r ^o and log K of the minerals considered by Lelli et al. (Environ Geol, 2007) and Accornero and Marini (Geobasi, 2007a; Proceedings of IMWA symposium, Cagliari, 27–31 May 2007b) was evaluated assuming ideal mixing in the solid state. These effects were found to be negligible for albite and the leucite–latitic glass, limited for muscovites and chlorites, and slightly more important for apatites. These influences become progressively higher with increasing concentration of trace elements in these minerals. Based on these deviations in thermodynamic parameters, special reactants should not include oxide components with molar fractions higher than 0.003. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.

Luigi MariniEmail:

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Heavy metals and rare earth elements (REEs) in soil from the Nam Co Basin,Tibetan Plateau   总被引：1，自引：0，他引：1  

Chaoliu Li  Shichang Kang  Xiaoping Wang  F. Ajmone-Marsan  Qianggong Zhang 《Environmental Geology》2008,53(7):1433-1440

Twenty-eight soil samples collected from the Nam Co Basin, Tibetan Plateau, have been analyzed for heavy metals (Cd, Cr, Ni, Cu, Zn, Pb and Mn), arsenic (As) and rare earth elements (REEs). In addition, for establishing the basic physio-chemical characteristics of the soil, pH, total organic concentration, electrical conductivity, and effective cation exchange capacity were measured. The results indicate that soil in the Nam Co Basin is still at an early alkaline weathering stage (pH = 7.94). Mean concentrations of heavy metals and As decreased as follows: Mn > Cr > Zn > Pb > Ni > Cu > As > Cd. The values of Cd, Cr, As, Pb and REEs in soil from the Nam Co Basin are higher relative to averaged background values over China. The chondrite-normalized diagrams of REEs suggest high REE(ΣLa → Eu)—enrichment, HREE(ΣGd → Lu)—depletion and Eu—depletion. Vertical profiles indicate that both heavy metals (except As) and REEs primarily exist in the surface soil. However, heavy metals and REEs vary in the surface soil between the southern and the northern bank of Nam Co. These differences are controlled mainly by parent materials.  相似文献   

Distribution of trace elements in the coastal sea sediments of Maslinica Bay, Croatia   总被引：1，自引：0，他引：1  

Nenad Mikulic  Visnja Orescanin  Loris Elez  Ljiljana Pavicic  Durdica Pezelj  Ivanka Lovrencic  Stipe Lulic 《Environmental Geology》2008,53(7):1413-1419

Spatial distributions of trace elements in the coastal sea sediments and water of Maslinica Bay (Southern Adriatic), Croatia and possible changes in marine flora and foraminifera communities due to pollution were investigated. Macro, micro and trace elements’ distributions in five granulometric fractions were determined for each sediment sample. Bulk sediment samples were also subjected to leaching tests. Elemental concentrations in sediments, sediment extracts and seawater were measured by source excited energy dispersive X-ray fluorescence (EDXRF). Concentrations of the elements Cr, Cu, Zn, and Pb in bulk sediment samples taken in the Maslinica Bay were from 2.1 to over six times enriched when compared with the background level determined for coarse grained carbonate sediments. A low degree of trace elements leaching determined for bulk sediments pointed to strong bonding of trace elements to sediment mineral phases. The analyses of marine flora pointed to higher eutrophication, which disturbs the balance between communities and natural habitats.  相似文献