汉诺坝玄武岩化学及其演化趋势

汉诺坝玄武岩于中新世喷出。除了碱性玄武岩以外,夏威夷岩广泛分布,还有苦橄玄武岩和马盖尔岩。有三个岩浆演化趋势:地壳岩浆房内橄榄石和单斜辉石斑晶组合的分离作用产生了从夏威夷岩到马盖尔岩的肯尼迪分异趋势;莫霍面附近的岩浆房内石榴石、普通辉石、歪长石和钛铁矿巨晶组合的分离作用导致了由原生夏威夷岩和碱性玄武岩经过进化的夏威夷岩和碱性玄武岩到拉斑玄武岩的跨式B型分异趋势;原生岩浆演化趋势。     

Stable Strontium Isotopic Fractionation During Chemical Weathering in Drainage Basins: Mechanisms and Applications

The new non-traditional stable strontium (Sr) isotope has aroused great attention from academic scholars in terms of the continental weathering and marine Sr cycle. The analytical precision of stable Sr isotope using mass spectrometry is better than 0.03‰. The compiled δ⁸⁸/ ⁸⁶Sr values vary from -3.65‰ to 1.68‰ in natural reservoirs. Recent findings indicate that multiple processes can cause stable Sr isotope fractionation in Earth surface, including the incongruent dissolution of primary minerals, the formation and adsorption of secondary minerals, the precipitation of calcium carbonate, and the biological cycling. These processes lead to higher δ⁸⁸/ ⁸⁶Sr in the liquid phase and lower δ⁸⁸/ ⁸⁶Sr in the solid phase, and thus result in different geochemical behavior of stable Sr isotopes in water and sediment during the weathering processes. The δ⁸⁸/ ⁸⁶Sr values of river sediment decrease with the increase of weathering intensity, which has the potential to indicate chemical weathering intensity. Meanwhile, further study on the fractionation mechanisms and constraints of stable Sr isotopes in river water plays an important role in tracing chemical weathering processes within the watershed, which will lead to a better understanding of the global ocean Sr cycle.     

Spatial distribution,fractionation and ecological risk assessment of potentially toxic metals in bottom sediments of the Zarivar freshwater Lake (Northwestern Iran)

Freshwater lakes are one of the most vulnerable ecosystems to environmental contamination. This study was initiated to assess the spatial distribution, fractionation, ecological risk of selected potentially toxic metals (Pb, Zn, Cu, Cr, and Ni) in bottom sediments of the Zarivar lake, the second largest freshwater lake in Iran. The results revealed that Pb, Zn and Cu had the high spatial variability (coefficient of variation >50) across the sampling sites and their maximum concentrations (197.5 for Pb, 198.7 for Zn and 185.6 mg/kg for Cu) were observed in sampling sites from the northern, western and eastern margins of the lake. Cr and Ni with average concentrations of 28.3 and 31.38 mg/kg respectively, exhibited low spatial variability (coefficient of variation <20) and their concentrations did not vary significantly among the sampling sites. Based on the redundancy analysis (RDA), sediment organic matter was strongly correlated with Pb, Zn and Cu while Fe₂O₃ and Al₂O₃ showed a positive correlation with Ni and Cr. The calculated average enrichment factor (EF) and geoaccumulation index (I_geo) showed that the contamination level of metals can be arranged in the following order of Pb> Cu > Zn > Cr > Ni. Results from the modified five-step sequential extraction analysis indicated that 40 % of total Pb and Zn were associated with the reducible fraction, 45 % of Cu with the oxidizable fraction and more than 80 % of total Ni and Cr were retrieved from the residual fraction. It was also noticed that Pb, Zn and Cu were more incorporated into the non-residual fractions in the sites with a higher total concentration of these metals, suggesting that both total concentration and fractionation behavior of metals were influenced by their potential sources in the study area. Ecological risk assessment using the potential ecological risk index (PERI) and the modified potential ecological risk index (MPERI) showed that sediments from the eight sampling sites pose a moderate to considerable risk whereas the other sites had low ecological risk level. In comparison to sediment quality guidelines (SQGs), the effects range low (ERL) and probable effect level (PEL) values for Pb, Cu and Zn were exceeded at some sampling sites while Ni and Cr concentrations were found to be below or close to their SQGs values at all the sampling sites. Pb was generally identified as the contaminant of most concern in the study area. Taking into account the results obtained from the fractionation study and the source contribution estimate, it can be inferred that the Pb, Zn and Cu with the average contribution of 79, 54 and 64 % respectively, were mainly derived from anthropogenic sources whereas Ni and Cr with the estimated contribution of 80 and 89 % were predominately from the lithogenic source.     

Petrogenesis and tectonic implications of Indosinian granitoids from Western Qinling Orogen,China:Products of magma-mixing and fractionation

The Western Qinling Orogen(WQO) is characterized by voluminous distribution of Indosinian granitoids,the formation of which provides an important window to unravel the geochemical and geodynamic evolution and associated metallogeny.Here we investigate a group of intrusions termed "Five Golden Flowers" based on petrological,geochemical,zircon U-Pb geochronological and Lu-Hf isotopic studies on the granitoids and their mafic microgranular enclaves(MMEs).Our results show that these intrusions are genetically divided into two types,namely,magma-mixing and highly fractionated.The Jiaochangba,Lujing,Zhongchuan,and Luchuba granitoids are biotite monzogranites(220±0.8 Ma to 217±2.6 Ma) with abundant coeval MMEs(220±.1 Ma to 217±2.7 Ma).The rocks contain moderate to high SiO_2,high MgO,Rb,Sr,Ba,and Th contents,but low TiO_2,P_2 O_5,and Sc values,A/CNK of 1.1,and a range of ε_(Hf)(t) values of-11.7 to +2.23 with corresponding T_(DM2)values of 1967-1228 Ma.The MMEs possess K-feldspar megacrysts,abundant acicular apatites,and show lopsided textures.They have lower SiO_2,Al_2 O_3,and Th contents,but higher MgO,TiO_2,and Sc,with ε_(Hf)(t) values of-18.0 to +3.18 and T_(DM1) of 849-720 Ma.The data indicate that the MMEs were derived from a magma sourced from the enriched lithospheric mantle.We suggest that these host granitoids were produced by partial melting of latePaleoproterozoic to early-Mesoproterozoic lower crust with the involvement of Neoproterozoic SCLM-derived mafic magmas.The Baijiazhuang pluton is dominantly composed of leucogranite(muscovite granite and twomica monzogranite,216±1.5 Ma) without MMEs.The rocks are peraluminous with high A/CNK(1.06-1.27).Compared with the other four granitoids,the Baijiazhuang leucogranite shows higher SiO_2 content,markedly lower concentrations of TiO_2,MgO,Al_2 O_3,CaO,and Fe_2 O_3~T,and lower LREE/HREE and(La/Yb)N values.These leucogranites are also rich in Rb,Th,and U,and display marked depletions in Ba,Sr,Ti,and Eu,indicating that they experienced significant fractionation.Zircon ε_(Hf)(t) values(-10.2 to-3.27) and T_(DM2)(1868-1424 Ma),as well as the Nb/Ta and K_2 O/Na_2 O values are similar to the other four granitoids,indicating that they are likely to have been derived from a similar source;with sediments playing only a minor role in the magma generation.The low contents of Yb and Y suggest that their partial melting was controlled by garnets and micrographic texture of K-feldspar reflects high-temperature melting through undercooling.Based on the above features,we infer that the Baijiazhuang leucogranite likely represents the product of high degree fractionation of the I-type biotite monzogranite magma which generated the other four granitoids at relatively high temperatures,within magma chambers at mid-crust depths.We propose that the granitoid suite was formed in the transitional setting from synto post-collision during the collisional orogeny between the SCB and NCB,following break-off of the subducted South China Block lithosphere during 220-216 Ma.     

Rare earth element fractionation in magmatic Ca-rich garnets

Igneous garnets have the potential to strongly fractionate rare earth elements (REE). Yet informations on partition coefficients are very scant, and criteria for distinguishing between hydrothermal and magmatic garnets are ambiguous. To fill this gap, we present trace element and isotopic data for two types of Ca-rich garnets from phonolites (Mt. Somma-Vesuvius). Both Ca-garnet populations are different in their style and dynamics of fractionation: one population is progressively strongly depleted in HREE from core to rim, reflecting REE fractionation in the host phonolite via earlier-crystallized garnets. Such examples for extreme changes in HREE in garnets are only known for hydrothermal grandites by REE-bearing fluids. The second garnet population is homogeneous and formed in a closed system. Near-flat patterns between Sm and Lu confirm experimental data indicating lower D(Sm)/D(Lu) for Ca-rich garnets than for e.g. pyrope-rich garnets. It follows: D ^Grt/PhMelt for La = 0.5, Sm = 48 and Yb = 110.     

锂同位素地球化学研究进展

锂的两个稳定同位素(6Li和7Li)相对质量差较大,因此锂同位素分馏比较显著。由于分析测量技术的改进和完善,锂同位素地球化学近年来有了长足的发展。研究表明,温度是控制锂同位素分馏的一个重要因素。此外,锂在不同矿物中配位结构和化学键强度的差异也会影响共存相之间的锂同位素分馏。由于锂同位素存在较大的分馏和不同地质体中截然不同的δ7Li值,锂同位素地质应用范围十分广泛。目前,锂同位素在地表风化、海底热液和洋壳蚀变、板块俯冲、示踪卤水来源和演化等方面的研究中成效显著,并且开始应用到矿床学中。     

Kerogen based characterization of major gas shales: Effects of kerogen fractionation

Research into the origin and the mode of entrapment and expulsion of natural gas from unconventional plays requires the isolation and separation of kerogen in its purest and most intact form from the rock matrix. This study expands on the comparative analysis of the effects that isolation methods, conservative closed system versus conventional open system, have on kerogen’s elemental, isotopic and physical properties. Four major gas shales, including the Barnett, the Marcellus, the Haynesville and a Polish gas shale, were chosen. In addition, the Monterey shale, though not strictly a gas shale, was included to address the effects on sulfur rich, Type II-S kerogen.Results indicate that the kerogen residues from the conventional open system method showed lower recovery and higher mineral content than those from the conservative closed system method. Differences were manifested in the elemental analysis data, where kerogens isolated using the open system method showed a significant deficit in the organic C, H, O, S and N material balance. Furthermore, the recovered residues show different sulfur content and δ³⁴S composition, most likely attributable to differences in pyrite content. Nevertheless, the relative abundances of the various macerals in the kerogen residues from the same parent shale are not very different; neither was the bulk δ¹³C composition of the recovered residues. This is not particularly surprising, considering that in all the five cases examined in this study, the organic matter was fairly homogeneous.     

Dinosterol δD values in stratified tropical lakes (Cameroon) are affected by eutrophication

In freshwater settings, dinosterol (4α,23,24-trimethyl-5α-cholest-22E-en-3β-ol) is produced primarily by dinoflagellates, which encompass various species including autotrophs, mixotrophs and heterotrophs. Due to its source specificity and occurrence in lake and marine sediments, its presence and hydrogen isotopic composition (δD) should be valuable proxies for paleohydrological reconstruction. However, because the purity required for hydrogen isotope measurements is difficult to achieve using standard wet chemical purification methods, their potential as a paleohydrological proxy is rarely exploited. In this study, we tested δD values of dinosterol in both particulate organic matter (POM) and sediments of stratified tropical freshwater lakes (from Cameroon) as a paleohydrological proxy, the lakes being characterized by variable degrees of eutrophication. In POM and sediment samples, the δD values of dinosterol correlated with lake water δD values, confirming a first order influence of source water δD values. However, we observed that sedimentary dinosterol was D enriched from ca. 19 to 54‰ compared with POM dinosterol. The enrichment correlated with lake water column conditions, mainly the redox potential at the oxic–anoxic interface (E_h OAI). The observations suggest that paleohydrologic reconstruction from δD values of dinosterol in the sediments of stratified tropical lakes ought to be sensitive to the depositional environment, in addition to lake water δD values, with more positive dinosterol δD values potentially reflecting increasing lake eutrophication. Furthermore, in lake sediments, the concentration of partially reduced vs. non-reduced C₃₄ botryococcenes, stanols vs. stenols, and bacterial (diploptene, diplopterol and ββ-bishomohopanol) vs. planktonic/terrestrial lipids (cholesterol, campesterol and dinosterol) correlated with E_h OAI. We suggest using such molecular proxies for lake redox conditions in combination with dinosterol δD values to evaluate the effect of lake trophic status on sedimentary dinosterol δD values, as a basis for accurately reconstructing tropical lake water δD values.     

稳定氯同位素及其应用地球化学研究

稳定氯同位素的分馏作用有限,同位素比值变化小,测定精度要求高。在很长一段时期内,人们一直未能发现自然界稳定氯同位素组成的变化。随着测定技术的不断发展,氯同位素的分馏效应逐渐得到证实,并引起了人们的广泛关注。国内外学者已将氯同位素应用于海水、地表河流水、地下水、盐湖、古代蒸发岩(盐)和热液矿床等方面的地球化学研究中,对水体演化和矿床成因进行了较为深入的探讨和分析,并取得了一定的研究进展。这些研究工作充分表明氯同位素在水体演化和成矿理论研究以及矿产勘查等方面有着独特优势,尤其在我国开展蒸发岩(盐)氯同位素地球化学研究具有很大的发展潜力和广阔的应用前景。但氯同位素的应用地球化学研究目前尚处于发展时期,更深入的研究还有待于测定方法的进一步完善以及对不同地球化学体系氯同位素的系统测定和研究。     

Phosphorus in suspended matter and sediments of a hypertrophic lake. A case study: Lake Dianchi,China

From June 2004 to December 2004, Lake Dianchi, which had large scale of cyanobacterial blooms was investigated in order to study P-fractionation in the suspended matter and the sediment. The investigation improves our understanding of phosphorus in Lake Dianchi and the relationship between phosphorus and cyanobacterial blooms. It contributes to the available literature on the behavior of P in hypertrophic lakes. The distribution of P-fractions in Lake Dianchi was not uniform from northwest to south, but was closely related to the trophic status of the whole lake. The concentrations of total phosphorus, labile P (NH₄Cl-P), Organic P (NaOH-NRP) and loss on ignition in suspended matter were positively correlated with the strength of cyanobacterial blooms. Total phosphorus in suspended matter was relatively stable for almost half an year and closely related to Chl. a concentration. The main content of organic phosphorus is in the cyanobacterial blooms. The concentrations of phosphorus bound to metal oxides and carbonates (NaOH-SRP and HCl-P) in sediment were similar to NaOH-SRP and HCl-P in the corresponding suspended matter. The latter two forms of P in suspended matter were not affected by cyanobacterial blooms, indicating that the inorganic phosphorus is derived from the sediment after resuspension from the sediment due to wind and wave action. The contribution of the different P-fractions to TP in sediment and in suspended matter indicates that NH₄Cl-P in the suspended matter is an important buffer for maintaining dissolved phosphorus in water.