鄂西长阳ZK04钻孔埃迪卡拉系陡山沱组C同位素组成特征及其地层对比意义

对湖北长阳两河口ZK04钻孔岩心进行了详细的碳酸盐岩C、O同位素分析,识别了埃迪卡拉系陡山沱组4次明显的δ~(13)C负偏离,分别位于陡山沱组一段、二段中上部、二段上部和三段上部至四段。其中第1、2和4次δ~(13)C负偏离与黄陵背斜周缘的剖面能够很好地对应,具有重要的区域和全球地层对比意义。在第1次δ~(13)C正偏离区域内并未发现明显的δ~(13)C负偏,分析认为WANCE事件可能仅代表了峡东部分地区一次短暂的δ~(13)C降低事件。第3次δ~(13)C负偏离表现最显著,然而在秭归泗溪和青林口以外的其他地区未见报道,可能是由于水体较浅的区域发生了地层缺失,未能保存此次δ~(13)C负偏离。长阳ZK04孔陡山沱组顶部的第4次δ~(13)C负偏离表现较弱,考虑到陡山沱组四段的黑色页岩较少发育,推测长阳两河口地区在陡山沱晚期处于浅水台地或台地边缘。DOUNCE可能是地史时期最大的一次全球性C同位素负偏离事件,其与大型具刺疑源类化石群和埃迪卡拉生物群的发展演化有紧密的联系,对于全球埃迪卡拉纪统级地层对比具有重要的意义。     

沾化凹陷新近系沉积物的C、O、Sr、Nd同位素组成变化对古环境变迁的记录

沾化凹陷新近系馆陶组(Ng)广泛发育了一陆相螺化石层.来自螺化石层上下沉积层位的馆陶组和明化镇组(Nm)泥灰岩的C、O、Sr、Nd同位素的分析结果显示,螺化石层所在Ng4段泥灰岩具有比其上下部泥灰岩较低的δ13C值和较高的δ18O值,而螺化石埋藏层位的泥灰岩具有相对较低的δ13C和87Sr/86Sr值以及相对较高的δ18O值.143Nd/144Nd比值在剖面上的变化不明显,反映Ng、Nm沉积时期凹陷具有稳定的物源区;而C、O、Sr同位素组成的系统变化则指示了古沉积环境的变化.其中Ng4段沉积时期气候相对干热,Ng3、Nm1 2段沉积时期气候相对湿热;螺化石层泥灰岩所表现出的低87Sr/86Sr值和螺化石壳体相对高的δ13C和δ18O值可能代表了区域上一次重要的气候干热化事件,该时期大气降水明显减少,湖泊蒸发量较大,使得盆地的水体盐度增加,水体中87Sr/86Sr降低和δ18O值增加,同时水体营养生物和河流输入的营养物质减少,致使田螺最终死亡.随后环境气候相对湿热,生物生产力提高和碎屑物质供应的增加使得87Sr/86Sr值和δ13C值增加,大气降水补给导致沉积介质的δ18O值降低.     

冀北宽城中元古界杨庄组地球化学特征

为分析碳酸盐岩地球化学特征对地层及层序界线、沉积环境的影响,选取冀北宽城中元古界杨庄组剖面进行了实测。冀北宽城中元古界杨庄组常量、微量元素和碳、氧同位素在纵向上具有特征的演变规律,特别是在岩石地层界线与层序界面附近变化明显。CaO含量从杨庄组一段到二段为21.07%～16.45%,从二段至三段则为16.45%～24.21%,Sr、Ba含量分别从杨庄组底部向上由44.59×10-6突变至98.16×10-6和0.51×10-6至10.45×10-6,δ13C值在0‰～-1.5‰之间变化,δ18O在-3.5‰～-8.5‰之间变化。上述常量、微量元素及碳、氧同位素组成、变化与同时期海平面变化基本一致,表明地球化学特征可作为划分地层界面或层序界面的标志,特别是可以优化地层界线或层序界线。杨庄组CaO/MgO、Sr/Ba及V、Rb、Be、B等组成和演化研究表明,杨庄组形成于干热气候下的近岸浅水环境。     

鄂尔多斯盆地巴汗淖地区马五_6段碳酸盐岩C、O同位素特征及其成岩意义

鄂尔多斯盆地北部巴汗淖地区马五6段为风化壳型碳酸盐岩地层,岩性以鲕粒灰岩、晶粒白云岩为主,次生孔隙发育,是重要的油气储集层。采用Finnigan MAT252气体同位素质谱仪分别对该段碳酸盐岩进行C、O同位素测试,详细分析了巴汗淖地区马五6段碳酸盐岩成岩环境及孔隙演化条件。样品分析结果表明:埋藏高温成岩环境使得δ18O值与奥陶纪海水的δ18O值相比明显偏负,且白云岩δ18O值与灰岩δ18O值相比偏负,主要是埋藏白云石化作用的结果;δ13C值与奥陶纪海水δ13C值相当,极个别数值偏负,说明研究区马五6段在成岩作用过程中受有机碳影响较小,表明成岩作用发生在浅-中埋藏条件下。研究区孔隙度、渗透率的相关关系明显,主要是大气淡水成岩作用的改造,优化了孔隙及渗流通道,提高了储层的物性。     

湖北宜昌峡东地区震旦系层型剖面化学地层特征及其国际对比

全球末元古系建系研究是当前国际地层学研究的重要课题之一。我国宜昌峡东地区震旦系沿江剖面研究历史悠久,已有相当深入的岩石地层、生物地层及层序地层研究,并被推荐为国际末元古系候选层序剖面之一。为进一步提高其研究精度,本文系统地研究了震旦系沿江剖面碳酸盐岩同位素化学地层。研究结果表明,陡山沱组底部“碳酸盐岩帽”的δ~(13)C为-3.1‰～-3.7‰,向上为正偏移,至层序Ⅲ(DS3)最大值达+6.7‰。陡山沱组顶部(DS6)再次出现负偏移-2.5‰,构成一个完整的变化周期。同时,~(87)Sr/~(86)Sr值表现出向上增大的变化,由陡山沱组底部(DS1)的0.707743逐渐增高至陡山沱组顶部(DS6)的0.707965;灯影组蛤蟆井段(DS7)的δ~(13)C值变化在-2.5‰～+5‰之间(DS8),至石板滩段中部再次降至+1.7‰(DS10),而后基本保持在+1.7‰～3.6‰之间平稳变动。白马沱段顶部δ~(13)C再次降至+0.5‰,并有向负偏移的趋势。灯影组的~(87)Sr/~(86)Sr值依然出现由老至新递增的趋势(0.708244～0.708993)与当前国际末元古系剖面的化学地层特征基本一致。     

四川盆地东南地区林1井灯影组鞍形自云石成因及其意义

对四川盆地东南地区林1井上震旦统灯影组鞍形白云石的岩相学特征和碳、氧、锶同位素特征及流体包裹体成分与温度进行研究,认为它属热液成因.研究区热液活动在岩相学上表现为充填状鞍形自云石,发育鞍形白云石线状充填晶洞.鞍形白云石共生矿物包括石英、沥青等.鞍形白云石δ18O值和δ13C值异常偏负,87Sr/86Sr值异常偏高,与围...     

准噶尔盆地东缘中侏罗统头屯河组层序地层与沉积演化

为揭示准噶尔盆地东缘中侏罗统头屯河组(J2t)层序地层特征及其沉积充填规律,结合露头、岩心及测井资料并运用高分辨率层序地层理论,对研究区头屯河组层序地层进行划分对比,对其沉积相展布特征和沉积环境演化规律进行研究。结果表明:头屯河组可划分出个1个Ⅲ级旋回、3个Ⅳ级旋回及9个Ⅴ级旋回,沉积物岩性以砂砾岩和泥岩为主,沉积环境主要为辫状河、辫状河三角洲和滨浅湖,发育向上"变深"对称型和非对称型的两种结构类型。头屯河组沉积时期湖泊较浅,沉积基底平缓,湖泊边缘坡度小,在头屯河组下段(J2t1)时期到头屯河组上段(J2t2)段时期经历了湖侵演变过程。结合研究区的层序地层和沉积相展布特征,认为研究区中侏罗统头屯河组具有辫状河、辫状河三角洲及湖泊3种沉积环境相结合的沉积演化模式。     

内蒙古大青山地区中、上侏罗统大青山组的修订

内蒙古大青山地区侏罗纪地层发育齐全 ,下、中侏罗统五当沟组为一套含煤碎屑沉积 ,中侏罗统长汉沟组为灰绿色粉细砂岩夹灰岩及砂砾岩 ,中、上侏罗统大青山组为紫色碎屑岩系 ,构成了一个完整的盆地演化序列。由于区内中生代逆冲推覆构造极其发育 ,使得区内不同时代的地层均呈构造岩片相互叠置 ,给地层划分和对比带来许多困难 ,前人所划分的中、上侏罗统大青山组 ,其中绝大部分并非大青山组 ,而是上二叠统脑包沟组和下白垩统李三沟组及固阳组。通过大量的野外调查工作 ,笔者对区内大青山组的地层层序、展布规律以及与下伏地层的接触关系性质等都重新给予厘定 ,提出大青山地区上侏罗统大青山组为一套干旱炎热气候条件下的河湖相沉积、生物贫乏 ,分布严格受坝岩—席麻湾—金銮殿断裂控制 ,与下伏地层局部呈不整合 ,整体呈假整合接触 ,这些结论对区内地层划分、对比以及地质演化历史的研究具有重要意义。     

松南长岭地区沉积层序演化与成藏要素特征研究

研究基准面升降和可容纳空间增减的变化,将长岭地区坳陷层泉四段-嫩一段地层划分为5个三级层序、8个四级层序,建立高精度层序地层格架.其地层纵向上表现为两期三角洲与湖泊沉积体系交互叠置的演化序列,反映出两次大的湖平面旋回变化.在层序地层格架内分析成藏要素的发育特征及其与沉积层序演化的有机联系.将坳陷期地层划分为三套有成因联...     

川东北地区长兴组白云岩储层的成因研究

以岩石结构与白云石Mg/Ca比值和有序度分析为基础,结合Sr,Fe,Mn微量元素和C,O,Sr同位素地球化学特征,对川东北地区上二叠统长兴组白云岩成因进行研究,结果表明长兴组白云岩有准同生白云岩和埋藏白云岩两种成因类型,储层只是埋藏白云岩化作用的产物,其形成过程可划分为早、中、晚3个成岩阶段,各成岩阶段埋藏白云岩化流体都来自于上覆地层飞仙关组的高盐度海源地层水,证据包括如下几个方面:①埋藏白云岩的岩石学特征明显地有别于准同生白云岩;②长兴组各类白云岩的Sr,Fe,Mn微量元素特征表明埋藏白云岩作用发生在无大气水影响的封闭体系中;③白云岩的C,O同位素组成特征符合埋藏白云岩的δ13C和δ18O分布区间;④长兴组与飞仙关组埋藏白云岩的Sr,Fe,Mn微量元素和Sr同位素地球化学特征基本一致。     

Isotopic systematics of He,Ar, S,Cu, Ni,Re, Os,Pb, U,Sm, Nd,Rb, Sr,Lu, and Hf in the rocks and ores of the Norilsk deposits

This paper reports the first results of a study of 11 isotope systems (³He/⁴He, ⁴⁰Ar/³⁶Ar, ³⁴S/³²S, ⁶⁵Cu/⁶³Cu, ⁶²Ni/⁶⁰Ni, ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ^206–208Pb/²⁰⁴Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others.     

高压微波消解法测定醋酸纤维过滤器采集的微尘粒子中的砷镉钴铬铜铁锰镍铅钒锌

最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提     

Wavelength-dispersive X-ray fluorescence spectrometric determination of Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites

Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours.     

Roles of xenomelts,xenoliths, xenocrysts,xenovolatiles, residues,and skarns in the genesis,transport, and localization of magmatic Fe-Ni-Cu-PGE sulfides and chromite

Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations.     

Regional distribution of Al,B, Ba,Ca, K,La, Mg,Mn, Na,P, Rb,Si, Sr,Th, U and Y in terrestrial moss within a 188,000 km2 area of the central Barents region: influence of geology,seaspray and human activity

Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km² area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population).     

Mercury,arsenic, antimony,and selenium contents of sediment from the Kuskokwim River,Bethel, Alaska,USA

The Kuskokwim River at Bethel, Alaska, drains a major mercury-antimony metallogenic province in its upper reaches and tributaries. Bethel (population 4000) is situated on the Kuskokwim floodplain and also draws its water supply from wells located in river-deposited sediment. A boring through overbank and floodplain sediment has provided material to establish a baseline datum for sediment-hosted heavy metals. Mercury (total), arsenic, antimony, and selenium contents were determined; aluminum was also determined and used as normalizing factor. The contents of the heavy metals were relatively constant with depth and do not reflect any potential enrichment from upstream contaminant sources.     

Petrographic, mineralogy, and geochemistry of coals of Pabedana, Kerman Province, Central Iran

This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds.     

Alkaline rocks of Samchampi-Samteran, District Karbi-Anglong, Assam, India

The Samchampi-Samteran alkaline igneous complex (SAC) is a near circular, plug-like body approximately 12 km² area and is emplaced into the Precambrian gneissic terrain of the Karbi Anglong district of Assam. The host rocks, which are exposed in immediate vicinity of the intrusion, comprise granite gneiss, migmatite, granodiorite, amphibolite, pegmatite and quartz veins. The SAC is composed of a wide variety of lithologies identified as syenitic fenite, magnetite ± perovskite ± apatite rock, alkali pyroxenite, ijolite-melteigite, carbonatite, nepheline syenite with leucocratic and mesocratic variants, phonolite, volcanic tuff, phosphatic rock and chert breccia. The magnetite ± perovskite ± apatite rock was generated as a cumulus phase owing to the partitioning of Ti, Fe at a shallow level magma chamber (not evolved DI = O1). The highly alkaline hydrous fluid activity indicated by the presence of strongly alkalic minerals in carbonatites and associated alkaline rocks suggests that the composition of original melt was more alkalic than those now found and represent a silica undersaturated ultramafic rock of carbonated olivine-poor nephelinite which splits with falling temperature into two immiscible fractions—one ultimately crystallises as alkali pyroxenite/ijolite and the other as carbonatite. The spatial distribution of varied lithotypes of SAC and their genetic relationships suggests that the silicate and carbonate melts, produced through liquid immiscibility, during ascent generated into an array of lithotypes and also reaction with the country rocks by alkali emanations produced fenitic aureoles (nephelinisation process). Isotopic studies (δ¹⁸O and δ¹³C) on carbonatites of Samchampi have indicated that the δ¹³C of the source magma is related to contamination from recycled carbon.