New data on Sr-and C-isotopic chemostratigraphy of the Upper Riphean type section (Southern Urals)     

A. B. Kuznetsov  M. A. Semikhatov  A. V. Maslov  I. M. Gorokhov  E. M. Prasolov  M. T. Krupenin  I. V. Kislova 《Stratigraphy and Geological Correlation》2006,14(6):602-628

New data on Sr-and C-isotopic systematics of carbonate rocks from the Upper Riphean stratotype (Karatau Group of the southern Urals) are obtained for several southwestern sections of the Bashkirian meganticlinorium, which have not been studied before. The results obtained supplement the Sr-and C-isotopic information for the group upper horizons thus detailing chemostratigraphic characterization of the entire succession. Limestone and dolostone samples used to analyze the Sr isotope composition satisfy strict geochemical criteria of the isotopic system retentivity and have been subjected to preliminary treatment in ammonium acetate to remove secondary carbonate phases. Data on 255 samples of carbonate rocks (171 studied for the first time) show that δ¹³C value varies in the Karatau Group succession from ?2.8 to +5.9 ‰ V-PDB with several in-phase excursions from the general trend in all the sections studied in the area 90 × 130 km. The δ¹³C variation trend demarcates several levels in the carbonate succession of the Karatau Group suitable for objectives of regional stratigraphy and for C-isotope chemostratigraphic subdivision of the Upper Riphean. The results of Sr isotopic analysis of 121 samples (51 unstudied before) from the Karatau Group imply that rocks in its lower part (the Katav Formation and basal horizon of the Inzer Formation) experienced considerable secondary alterations, while limestones and dolostones of the overlying interval of the group are frequently unaltered. In the “best” samples satisfying geochemical criteria of the isotopic system retentivity, the ⁸⁷Sr/⁸⁶Sr initial ratio increases from 0.70521–0.70532 in the lower Inzer deposits to 0.70611 in the upper Min’yar carbonates, decreasing to <0.70600 near the top of the latter. Above the regional hiatus separating the Min’yar and Uk formation, this ratio grows from 0.70533 to 0.70605–0.70609 in the limestone succession of the last formation.  相似文献   

Metal sources of the Navan carbonate-hosted base metal deposit, Ireland: Nd and Sr isotope evidence for deep hydrothermal convection     

R. D. Walshaw  J. F. Menuge  S. Tyrrell 《Mineralium Deposita》2006,41(8):803-819

Nd and Sr isotope analyses are presented for gangue mineral samples from the giant carbonate-hosted Navan Zn–Pb deposit, Ireland, and for rocks from which Navan metals may have been derived. Analysis of gangue minerals spanning the Navan paragenetic sequence reveals systematic evolution in the composition of the mineralising fluid. Early fluid represented by replacive dolomite exhibits the lowest initial ⁸⁷Sr/⁸⁶Sr ratio (0.7083–0.7086), closest to that of the host limestone and to Lower Carboniferous seawater, and the highest ¹⁴³Nd/¹⁴⁴Nd ratio (0.51161–0.51176). Later generations of dolomite, barite and calcite, which encompass sulphide precipitation, have higher initial ⁸⁷Sr/⁸⁶Sr ratios (maximum 0.7105) and lower initial ¹⁴³Nd/¹⁴⁴Nd ratios (minimum 0.51157). All samples have initial Nd isotope ratios that are too low to have been acquired only from the host limestone. Drill core samples of presumed Ordovician volcanic and sedimentary rocks from beneath the Navan orebody have ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr ratios at the time of mineralisation of 0.51184–0.51217 and 0.7086–0.7138, respectively. The data are interpreted to indicate mixing of sulphide-rich, limestone-buffered brine, with a metal-bearing hydrothermal fluid, which had passed through sub-Carboniferous rocks, consistent with published fluid inclusion and S isotope data. The ¹⁴³Nd/¹⁴⁴Nd ratio of this basement-derived fluid is too low to have been imparted by flow through the Devonian Old Red Sandstone, as required in models of regional fluid flow in response to Hercynian uplift. Irrespective of whether such regional fluid flow occurred, the hydrothermal Nd must have been derived from sub-Devonian rocks. These conclusions broadly support the hydrothermal convection cell model in which brines, ultimately of surface origin, penetrated to a depth of several kilometres, leaching metals from the rocks through which they passed. The data also support increasing depth of penetration of convection cells with time. Metals were subsequently precipitated in carbonate rocks at sites of mixing with cooler, sulphide-rich fluids. However, comparison of the Navan hydrothermal gangue Nd–Sr isotope data with data from Lower Palaeozoic rocks strongly suggests that the latter cannot alone account for the “basement” signature. As the Navan deposit lies immediately north of the Iapetus Suture, this suggests that the Laurentian margin includes Precambrian basement.  相似文献   

Synchrotron IR study of hydrous ringwoodite (γ-Mg2SiO4) up to 30 GPa     

E. M. Chamorro Pérez  I. Daniel  J.-C. Chervin  P. Dumas  J. D. Bass  T. Inoue 《Physics and Chemistry of Minerals》2006,33(7):502-510

High-pressure synchrotron infrared (IR) absorption spectra were collected between 650 and 4,000 cm⁻¹ at ambient temperature for hydrous Mg-ringwoodite (γ-Mg₂SiO₄) up to 30 GPa. The main feature in the OH⁻ stretching region is an extremely broad band centred at 3,150 cm⁻¹. The hydrogen bond is strong for most protons and the most probable site for protonation is the tetrahedral edge. With increasing pressure, this band shifts downward while decreasing its integrated intensity until disappearance at a pressure of 25 GPa. Only one band at 2,450 cm⁻¹ and an absorption plateau persist with a maximum wavenumber of 3,800 cm⁻¹. This behaviour is reversible upon pressure release. We interpret this as a second-order phase transition occurring in hydrated Mg-ringwoodite at high pressure (beyond ∼ 25 GPa). This result is compatible with the observation by Kleppe et al. (Phys Chem Miner 29:473–476, 2002a) who suggested the presence of Si–O–Si linkages and/or partial increase in the coordination of Si. Beyond the phase transition, the protons are delocalized and their environment on the ringwoodite structure is probably quite different from that at low pressure. Data obtained in situ at high pressures and temperatures are needed to better understand the effect of protonation on the structure and to better constrain this phase transition.  相似文献   

一次“高影响天气”的弱降雪过程的数值研究   总被引：11，自引：2，他引：11       下载免费PDF全文

蒋建莹史历  倪允琪 《应用气象学报》2005,16(2):231-237

该文对2001年12月7日下午北京的一次弱降雪天气过程进行了诊断分析和数值模拟研究。诊断结果表明:北京地区由于受500 hPa小槽东移及850 hPa东移小高压后部带来的来自东海和南海的偏南暖湿气流共同影响，造成降雪。数值模拟结果显示:MM5模式对这次降雪过程具有较好的模拟能力，不仅模拟出了北京地区的降雪量，而且对这次过程大尺度背景场的演变、触发机制和水汽源有很好的表述。利用诊断分析和数值模拟结果，对这次弱降雪过程引起交通大阻塞的可能因素进行了探讨，说明建立城市预警系统的迫切性。  相似文献   

Electrical aerosol spectrometer of Tartu University     

H. Tammet  A. Mirme  E. Tamm   《Atmospheric Research》2002,62(3-4)

The electrical aerosol spectrometer (EAS) of the parallel measuring principle at Tartu University is an efficient instrument for rapid measurement of the unstable size spectrum of aerosol particles. The measuring range from 10 nm to 10 μm is achieved by simultaneously using a pair of differential mobility analyzers with two different particle chargers. The particle spectrum is calculated and measurement errors are estimated in real time by using a least-squares method. Experimental calibration ensures reliability of measurement. The instrument is well suited for continuous monitoring of atmospheric aerosol.  相似文献   

羌塘盆地那底岗日地区中侏罗世层序地层与碳、氧、锶同位素响应   总被引：7，自引：0，他引：7  

谢渊  王剑  刘家铎  罗建宁  张哨楠  杨宝星  李明辉 《沉积学报》2002,20(2):188-196

羌塘盆地那底岗日地区中侏罗世沉积了一套稳定的滨浅海相碳酸盐岩与碎屑岩地层,通过层序地层研究划分出五个三级层序。对其中四个层序内碳酸盐岩碳、氧、锶稳定同位素测试分析得出,不同层序、层序界面及层序内不同体系域的δ13 C、δ180、N(87Sr/86Sr)值均有明显的差异,并具规律性变化,整体上反映出研究区中侏罗世发生了多次海平面升降变化和气候、构造活动的演变,为层序地层研究提供了定量的地质地球化学依据。  相似文献   

铅锌矿床Rb-Sr定年研究综   总被引：10，自引：0，他引：10  

李文博  黄智龙  许德如  陈进  许成  管涛 《大地构造与成矿学》2002,26(4):436-441

本文在总结Rb-Sr等时线定年的基本前提和矿床Rb-Sr等时线定年存在的问题的基础上,综述了铅锌矿床流体包裹体和闪锌矿Rb-Sr等时线定年的研究进展,同时对该定年方法存在的问题进行了简要评述。综合分析表明,Rb-Sr等时线定年(尤其是闪锌矿Rb-Sr等时线定年)为铅锌矿床较理想的直接定年方法,但该定年方法还存在许多理论和技术问题,有待深入研究;铅锌矿床Rb-Sr等时线定年应以深入细致的地质、地球化学研究为基础,定年过程中必须严慎对待样品采集、样品挑选、流体包裹体溶液提取和质谱分析等各个环节。  相似文献   

Spectroscopic evidence for pressure-induced phase transitions in diopside     

A. Chopelas  G. Serghiou 《Physics and Chemistry of Minerals》2002,29(6):403-408

 Raman spectra of diopside were collected from atmospheric pressure to 71 GPa. The pressure dependences of 22 modes were determined. Changes occurred in the spectra at three different pressures. First, at approximately 10 GPa, the two Raman modes at 356 and 875 cm⁻¹ disappeared, while the mode at 324 cm⁻¹ split into two modes, diverging at this pressure with significantly different pressure shifts; second, at approximately 15 GPa, a small (1 to 2 cm⁻¹) drop in several of the frequencies was observed accompanied by changes in the pressure dependency of some of the modes; and third, above 55 GPa, the modes characteristic of chains of tetrahedrally coordinated silicon disappeared, while those for octahedrally coordinated silicon appeared. The first change at 10 GPa appears to be a C2/c to C2/c transition involving a change in the Ca coordination. The third change above 55 GPa appears to be a change in the silicon coordination. At 15 GPa, it is suggested that a change in compressional mechanism takes place. Received: 14 November 2000 / Accepted: 9 January 2002  相似文献   

Celestite formation, bacterial sulphate reduction and carbonate cementation of Eocene reefs and basinal sediments (Igualada, NE Spain)   总被引：5，自引：0，他引：5  

Conxita Taberner  James D. Marshall†  James P. Hendry‡  Catherine Pierre§  & M. F. Thirlwall¶ 《Sedimentology》2002,49(1):171-190

Petrographic and geochemical studies of an Upper Eocene reef and associated basinal sediments from the mixed carbonate–siliciclastic fill of the south‐eastern Pyrenean foreland basin near Igualada (NE Spain) provide new insights into the evolution of subsurface hydrology during the restriction of a marine basin. The reef deposits are located on delta‐lobe sandstones and prodelta marls, which are overlain by hypersaline carbonates and Upper Eocene evaporites. Authigenic celestite (SrSO₄) is an important component in the observed diagenetic sequences. Celestite is a significant palaeohydrological indicator because its low solubility constrains transportation of Sr²⁺ and SO₄^2? in the same diagenetic fluid. Stable isotopic analyses of carbonates in the reef indicate that meteoric recharge was responsible for aragonite stabilization and calcite cementation. Sulphur and oxygen isotope geochemistry of the celestite demonstrates that it formed from residual sulphate after bacterial sulphate reduction, but also requires that there was a prior episode of sulphate recycling. Meteoric water reaching the reef and basinal areas was most probably charged with SO₄^2? from the dissolution of younger Upper Eocene marine evaporites. This sulphate, combined with organic matter present in the sediments, fuelled bacterial sulphate reduction in the meteoric palaeoaquifer. Strontium for celestite precipitation was partly derived in situ from dissolution of aragonite corals in the reef and basinal counterparts. However, ⁸⁷Sr/⁸⁶Sr data also suggest that Sr²⁺ was partly derived from dissolution of overlying evaporites. Mixing of these two fluids promoted celestite formation. The carbonate stable isotopic data suggest that the local meteoric water was enriched in ¹⁸O compared with that responsible for stabilization of other reefs along the basin margin. Furthermore, meteoric recharge at Igualada post‐dated evaporite deposition in the basin, whereas other parts of the same reef complex were stabilized before evaporite formation. This discrepancy resulted from the spatial distribution of continental siliciclastic units that acted as groundwater conduits.  相似文献   

城市震害高危害小区的研究和GIS的实现技术   总被引：3，自引：2，他引：3  

帅向华  成小平  袁一凡 《地震》2002,22(3):113-119

论述了在城市地震灾害中如何考虑诸方面因素来评价城市的灾害轻重分布情况。中建立坑危害小区分析模型，设想将城市划分等面积网格，给每个单元网格赋予灾害指数，以确定城市中受灾较为严重的区域，为求灾指挥提供决策信息。同时，将高危害小区的模型研究结果转化为计算机技术可以实现的GIS模型。该研究结果已应用于泰安市防震减灾示范研究项目中。  相似文献