塔里木盆地西北缘奥陶系碳酸盐岩中两种来源热流体的地质与地球化学证据

塔里木盆地西北缘西克尔-巴楚-柯坪地区处于巴楚-柯坪断隆带活动区,构造活动强烈.该区出露的中下奥陶统鹰山组发育大量的热液蚀变现象,既有溶蚀形成的大小孔洞、疏松灰岩层,也有各类充填的脉体,如萤石矿、硫磺石膏矿等.通过野外露头观察和采样,并对受热流体作用的样品进行了包裹体测温测盐、微量元素和硫同位素分析.结果显示研究区主要有两种流体来源:岩浆热液和地层热液.研究表明:(1)岩浆热液主要影响研究区南西段,形成萤石、重晶石、方铅矿等矿物,流体包裹体盐度低(0.5％ ～7.5％ NaCleqv)、均一化温度相对较高(142 ～ 283℃);地层热液作用范围则主要位于研究区北东段,生成白云石、方解石、石英等矿物,流体包裹体盐度高(16％ ～ 23.3％ NaCleqv)、均一化温度低(70～ 138℃);而研究区中段同时受到两种来源热液的混合作用,包裹体盐度(7.5％～18.3％ NaCleqv)和均一化温度(142 ～ 163℃)介于前两者之间;(2)热液硬石膏、硫磺的硫同位素富含32S,δ4S平均为-9.57％,说明硬石膏是H2S气体与灰岩反应的产物,硫化氢很可能来自有机物的热裂解.     

A Multi‐Element Ion‐Pair Extraction for Trace Metals Determination in Environmental Samples

A multi‐element ion‐pair extraction method was described for the preconcentration of Cd(II), Co(II), Cr(III), Cu(II), Fe(III), Mn(II), Ni(II), Pb(II), and Zn(II) ions in environmental samples prior to their determinations by flame atomic absorption spectrometry (FAAS). As an ion‐pair ligand 2‐(4‐methoxybenzoyl)‐N′‐benzylidene‐3‐(4‐methoxyphenyl)‐3‐oxo‐N‐phenyl‐propono hydrazide (MBMP) was used. Some analytical parameters such as pH of sample solution, amount of MBMP, shaking time, sample volume, and type of counter ion were investigated to establish optimum experimental conditions. No interferences due to major components and some metal ions of the samples were observed. The detection limits of the proposed method were found in the range of 0.33–0.9 µg L^?1 for the analyte ions. Recoveries were found to be higher than 95% and the relative standard deviation (RSD) was less than 4%. The accuracy of the procedure was estimated by analyzing the two certified reference materials, LGC6019 river water and RTC‐CRM044 soil. The developed method was applied to several matrices such as water, hair, and food samples.     

Trace element and REE geochemistry of fine- and coarse-grained sands in the Ordos deserts and links with sediments in surrounding areas

In addition to mineral analyses, REE and trace element geochemical characteristics of fine- and coarse-grained sands in the Ordos deserts and other sediments in surrounding areas are investigated.Commonly the samples consist of quartz, feldspar and muscovite and less clinochlore, dolomite and ankerite. In few samples muscovite is absent.REE and trace compositions are spatially uniform for the same grain-size sands, suggesting that they could have the same sources or/and were well homogenized. However, fine- and coarse-grained sands in the Ordos deserts show different REE and trace element compositions. Fine-grained sands show higher contents of REE and trace elements than those of coarse-grained sands. They differ in Eu anomalies and (La/Yb)_N ratios although both fractions are characterized by the steep LREE and smooth HREE patterns. The fine- and coarse-grained sands are also distinct in some characteristic element ratios (e.g., Th/Co, La/Sc, Th/Sc and Y/Ni).REE and trace element patterns of the two different grain-size fractions are closely associated with geological properties of individual sources rather than the mineralogical differentiation induced by wind sorting. The coarse-grained sands mainly resulted from sandstone weathering in the Ordos deserts and movements of coarse particles by wind. REE and trace element patterns of fine-grained sands in the Ordos deserts differ from those of sandstones in the Ordos deserts, the alluvial sands in the surrounding mountains and the coarse fluvial sands in the Yellow River. They resemble the fine fluvial sands in the Yellow River. In addition, arid areas of Northwest China such as the Tarim Basin and the Alxa Plateau should not be ruled out as the source of the fine-grained sands in the Ordos deserts because these arid areas reserve plenty of fine-grained sediments and also located in the upwind directions of the Ordos deserts.     

Patterns of rare earth and other trace elements in different size fractions of clays of Campanian–Maastrichtian deposits from the Portuguese western margin (Aveiro and Taveiro Formations)

The Upper Cretaceous (Campanian–Maastrichtian) Taveiro and Aveiro Formations belong to the northern sector of the Lusitanian basin (Portuguese western margin). The Taveiro Formation was deposited in alluvial fans, including mud flow beds, lakes and sinuous rivers. The Aveiro Formation was deposited in a flat region with low hydrodynamics channels, with the formation of a barrier island-tidal system. The reconstruction of this sedimentary basin may be difficult due to its complex architecture. This work aims a methodology to be used in the reconstruction of Cretaceous sedimentary environments of the Lusitanian basin, through the establishment of geochemical patterns of different size fractions of those deposits. Chemical analysis was performed by instrumental neutron activation analysis (INAA), and the mineralogical composition obtained by X-ray diffractometry (XRD). The whole rock and different size fractions (? ≥ 125 μm, 63–125 μm, 20–63 μm, 2–20 μm and ? < 2 μm) of selected samples were studied aiming the rare earth elements (REE) and other trace elements distribution and its correlation with the grain size and mineralogy.The results obtained for the studied Cretaceous sediments showed that REE patterns and other trace elements distribution in the different size fractions may be used as a tool to differentiate deposits within and between sedimentary formations. Within the Taveiro Formation, REE are concentrated in the silt fractions (20–63 μm and 2–20 μm) of the Reveles deposit, and in the clay size fraction of S. Pedro deposit, which is richer in kaolinite. The 1st transition elements, particularly Zn, are correlated with the presence of smectite in the clay fraction of Reveles deposit. In the sand and silt size fractions (>2 μm) of samples from Taveiro Formation correlations were found between: Ga and 1st transition elements, and phyllosilicates; Cs and mica; and Rb and Ba, and K–feldspars.The Bustos deposit (Aveiro Formation) samples are very fine-grained and with a high proportion of the fine silt fraction where REE are concentrated, especially the heavy ones. Incorporation of MREE, Co and U in carbonates of the coarser fraction appears to occur. The abundances of the 1st transition elements, Ga and As, are correlated with phyllosilicates.Significant differences were found in the trace elements patterns of the various analysed size fractions of the Lusitanian basin of Cretaceous sediments, between and even within formations, which can be used as a methodological approach for a fine paleogeographic reconstruction.     

Geochemical environment of Cenomanian - Turonian black shale deposition at Wunstorf (northern Germany)

Major- and minor- element determinations were carried out on a high-resolution sample set obtained from a sediment drill core at Wunstorf (N. Germany). This study interval includes the black shale-bearing Hesseltal Formation associated with the Oceanic Anoxic Event 2 (OAE 2), also referred to as Cenomanian-Turonian Boundary Event (CTBE). Seven black shale packages, each containing several black shale layers, were defined by elevated TOC values, with black shale packages 1-4 deposited during OAE 2. Packages 5-7 extend above the level of the positive carbon-isotope excursion defining OAE 2, indicating that conditions favouring organic carbon burial must have prevailed longer in the Wunstorf Basin than elsewhere. Geochemical analyses revealed no significant differences between black shale packages deposited during and after OAE 2. Enrichment patterns of sulphur, iron and redox-sensitive and sulphide-forming trace metals point to suboxic to anoxic conditions existing at the sediment-water interface during black shale deposition, whereas sulphidic conditions prevailed deeper in the sediment. Variations in element/Al ratios follow cyclic patterns which are interpreted to represent climatically-induced changes in sediment supply. Reduced vertical mixing led to water-column stratification and caused black shale deposition.     

碳酸盐沉积物的成岩作用

化学沉淀碳酸盐矿物在沉积后很容易受到各种作用的影响,其中最重要的是其在成岩阶段所经历的成岩作用.碳酸盐沉积物在成岩过程中主要受大气降水、海水和埋藏过程中孔隙流体的控制,经历一系列压实、溶解、矿物的多相转变、重结晶、胶结等成岩作用,逐渐转变为固结的岩石.在成岩过程中,由于孔隙流体与沉积流体之间的异同以及温度的变化,碳酸盐沉积物的原始矿物成分、地球化学特征可能会很好的保存下来,但在许多情况下,也可能会改变,从而使我们无法准确反演碳酸盐沉积物在沉积时水体的特征.因此,我们在应用碳酸盐岩重建相关古环境和古气候变化的时候,必须要通过有效的方法来对碳酸盐岩是否受到成岩作用的影响进行鉴定.     

Assessment of the natural and anthropogenic sources of chemical elements in alluvial soils from the Drava River using multivariate statistical methods

The objectives of this study are as follows: (a) an assessment of the geochemical background signature of the Drava Valley before the industrial revolution; (b) an evaluation of anthropogenic geochemical influences on the alluvial plains and river terraces in the valley; and (c) a determination of the spatial distribution of trace elements in the alluvial soils of the Drava River downstream of the Austrian–Slovenian border to the confluence of Mura and Drava Rivers.     

示波极谱法测量电锌液中微量镍

提出在丁二酮肟-亚硝酸钠-氨水-氯化铵体系中,准确测定电锌液中微量镍的新方法:克服原子吸收光谱法测定微量镍回收率偏低问题。     

Geochemistry of the Jurassic and Upper Cretaceous shales from the Molango Region,Hidalgo, eastern Mexico: Implications for source-area weathering,provenance, and tectonic setting

This study focuses on the Jurassic (Huayacocotla and Pimienta Formations) and Upper Cretaceous (Méndez Formation) shales from the Molango Region, Hidalgo, Mexico. In this article, we discuss the mineralogy, major, and trace element geochemistry of the Mesozoic shales of Mexico. The goal of this study is to constrain the provenance of the shales, which belong to two different periods of the Mesozoic Era and to understand the weathering conditions and tectonic environments of the source region.     

云南香格里拉红山铜矿石硫化物环带及地质意义

云南香格里拉县红山铜矿是三江义敦岛弧带南端重要铜矿床,颇受关注,成因认识分歧大.矿区出露上三叠统板岩、变碎屑岩和灰岩夹中基性火山岩、火山碎屑岩以及少量侵入其中的中酸性和超基性岩脉、岩株,透镜状铜硫化物矿体产在顺层状矽卡岩体内或边部,成矿后断裂明显.矿石中普遍发育以黄铁矿为核部、黄铜矿为中间带、磁黄铁矿为边部带的硫化物环带,其中核部黄铁矿呈立方体自形-半自形晶,黄铜矿呈他形晶围绕黄铁矿沉淀,磁黄铁矿呈他形分布在黄铜矿外围,内带常被外带硫化物溶蚀交代.环带从内到外硫化物先后沉淀,矿物生成顺序为黄铁矿-黄铜矿-磁黄铁矿.环带中三种硫化物矿物的REE配分曲线和微量元素蛛网图极为相似,负Eu异常显著,富集U、Th、Zr、Hf,亏损Rb、Sr、Ba,与矿区超基性岩表现出较高相似性;环带从内到外,∑REE(0.17371×10-6、1.22626×10-6、5.25925×10-6)和微量元素含量依次升高,Co/Ni和Se/Te比值降低,指示矿石硫化物沉淀过程中,可能伴随热液体系内地壳物质不断增加.环带中硫化物矿物δ34SV-CDT=3.81‰～5.23‰,具有岩浆硫源特征,δ34SV-CDT边部带磁黄铁矿 (4.47‰)＜δ34SV-CDT中间带黄铜矿(4.58‰)＜ δ34SV-CDT核部黄铁矿(4.65‰),三种硫化物间没有达到同位素平衡分馏.红山铜矿石环带结构是岩浆热液为主成矿流体中黄铁矿、黄铜矿、磁黄铁矿先后晶出成因,伴随硫化物环带的形成,热液系统从早到晚H2S和O2逸度降低或pH升高过程.