首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 62 毫秒
1.
东胜铀矿床位于鄂尔多斯盆地的东北部,是我国新近发现的大型砂岩型铀矿床。铀矿体位于中侏罗统直罗组下段的辫状河道沉积砂体中,受灰色砂岩与灰绿色砂岩的接触带控制。灰绿色砂岩的化学成分中硅酸盐矿物二价铁含量高是该类型砂岩呈现绿色的重要原因。在矿物组成上,灰绿色砂岩主要表现为粘土矿物总量高,特别是绿泥石含量高。岩石学、矿物学和地球化学的证据表明,东胜铀矿区存在后生还原作用。灰绿色砂岩是控矿的古氧化岩石遭受还原性流体改造的产物,后生还原作用掩盖了古氧化蚀变带,并在一定程度上起到了保矿作用。东胜地区后生还原作用在时间上和成因上与河套断陷盆地的产生和形成具有密切联系。  相似文献   

2.
为查明鄂尔多斯盆地塔然高勒地区直罗组上段、下段的岩性-岩相特征以及参与蚀变作用的流体强度差异,开展了系统的岩心观察、剖面对比,并结合黏土矿物、碳氧同位素和U、Th元素等手段进行分析。结果表明,研究区南部直罗组上段主要由灰绿色、红色泥岩夹透镜状红色、黄色、灰绿色砂岩组成,北部主要由红色泥岩与灰绿色砂岩构成,南北部下段均由灰白色、灰绿色砂岩或砂砾岩夹薄层泥岩组成。直罗组红色砂岩为原生沉积,灰绿色砂岩为后生改造类型;上段受含氧含铀水和深部还原性流体作用强度较下段变弱,且由北向南作用程度降低,北部还原蚀变岩石与原生岩石共存,南部基本保留原生岩石;下段则受流体改造更为充分,主体为后生蚀变岩石。直罗组不同类型砂体的展布兼受沉积相和后期流体双重作用,但强弱差异性明显,限制了铀矿化产出在直罗组下段砂体中的定位,因此,上、下段应作为不同的成矿体系讨论。  相似文献   

3.
鄂尔多斯盆地北部东胜地区中侏罗统直罗组下段古层间氧化型砂岩铀矿较为发育,铀矿化主要发育于层间氧化带氧化前锋附近(灰绿色砂体与灰色砂体的过渡部位)。通过对测井资料的解释发现,东胜矿区深部西南部乌审旗西南和北部杭锦旗附近直罗组下段砂体中也存在放射性异常。通过对东胜深部矿区50多个钻孔的数据统计与分析,重现了直罗组下段(下亚段、上亚段)的古层间氧化-还原砂体的分布。古氧化带大致呈NW-SE向展布,主要分布在研究区中北部;放射性异常主要出现在氧化-还原过渡带部位。研究区目的层砂体内放射性异常总体呈现出厚度较小(下亚段异常层平均厚度2.67 m、上亚段异常层平均厚度2.33 m)、埋深较大(下亚段异常层平均埋深1 025 m、上亚段异常层平均埋深921 m)的特征。  相似文献   

4.
鄂尔多斯盆地东胜铀矿床成矿特征与成矿模式   总被引:18,自引:0,他引:18  
东胜铀矿床产于中侏罗统直罗组下段的辫状河道沉积砂体中,铀矿体受灰色砂岩与灰绿色砂岩的接触带控制。灰绿色砂岩的化学成分中硅酸盐矿物二价铁含量高是该类型砂岩呈现绿色的重要原因。在矿物组成上,灰绿色砂岩主要表现为粘土矿物总量高,特别是绿泥石含量高。岩石学、矿物学和地球化学的证据表明,东胜铀矿区存在后生还原作用。灰绿色砂岩是控矿的古氧化岩石遭受还原性流体改造的产物,后生还原作用掩盖了古氧化蚀变带,并在一定程度上起到了保矿作用。东胜地区后生还原作用在时间上和成因上与河套断陷盆地的产生和形成具有密切联系。铀在矿石中主要呈铀矿物和吸附形式存在。通过电子探针和X射线粉晶分析鉴定,确定东胜铀矿床矿石中的主要铀矿物为铀石,并含有少量钛铀矿和沥青铀矿。富矿石样品中铀石单矿物的铀铅同位素年龄集中分布于20~10 Ma之间。通过研究,建立了鄂尔多斯盆地东胜铀矿床的“多阶段铀成矿模式”,即“成岩期预富集层间渗入成矿再改造富集油气还原保护”的多阶段、多成因流体长期富集改造的铀成矿模式。  相似文献   

5.
红豆山铜矿床是南澜沧江带新发现的矿床之一。通过野外地质工作和系统构造—|蚀变岩相填图,发现该矿床蚀变类型主要以钾长石化、硅化、绿泥石化、绿帘石化为主,其次为碳酸盐化、绢云母化、黄铁矿化等,且在空间上呈现一定规律,各蚀变带具有明显的叠加现象。依据区内岩石蚀变矿物组合等特点,自断裂带→上盘围岩,共出现4个典型蚀变带,依次为碎裂岩化带→长英岩化—碳酸盐化—绢云母化带→硅化—绿泥石化—绿帘石化带→弱长英岩化安山岩带。矿(化)体主要分布在长英岩化、碳酸盐化、绢云母化带和硅化、绿泥石化、绿帘石化带。由斑岩脉中心至边缘发育钾化带→硅化带→青磐岩化带→绢云母化带,斑岩旁侧围岩中发育放射状石英—方解石—黄铜矿脉。  相似文献   

6.
内蒙古巴音戈壁盆地塔木素地区的铀矿化与中国北方其他盆地的层间氧化带砂岩型和泥岩型铀矿化明显不同。在该地区的铀矿化岩石中,砂岩和泥岩几乎各占一半,并且出现不同类型的后期改造。笔者通过野外露头、岩心观察和室内微观分析,发现该地区的矿化岩石发育赤铁矿化、褐铁矿化、黄钾铁矾化、碳酸盐化、石膏化和绿泥石化等多种蚀变。在查明各蚀变带特征的基础上,讨论了巴音戈壁组上段蚀变带的期次及与铀矿化的关系。研究认为,以赤铁矿化、褐铁矿化、黄钾铁矾化为标志的红色、黄色岩石氧化作用发育时间较早,而碳酸盐化、石膏化和绿泥石化较晚;铀矿化分布受氧化作用控制,而灰绿色蚀变所代表的后期热流体叠加作用,使铀矿化进一步富集。  相似文献   

7.
通过对鄂尔多斯盆地彬长地区直罗组后生蚀变特征进行系统研究,认为彬长地区中侏罗统直罗组存在早期紫红色氧化蚀变和晚期灰白色、灰绿色还原褪色蚀变两种蚀变类型。早期氧化蚀变的主要蚀变矿物为微粒状褐铁矿和褐铁矿集合体,而晚期灰白色、灰绿色褪色还原蚀变的蚀变矿物主要为黄铁矿、绿泥石以及部分残留未完全氧化的炭屑。研究区直罗组蚀变在垂向上分带明显,在垂向上铀矿化主要受灰绿色褪色蚀变砂体与原生灰色砂体的过渡部位控制,铀矿物主要为铀石,常分布于炭屑中且与黄铁矿伴(共)生;平面上,铀矿化产于氧化—还原过渡带内。  相似文献   

8.
通过对鄂尔多斯盆地东胜地区纳岭沟、大营铀矿床直罗组下段砂岩中139个样品的酸解烃分析,探讨了酸解烃中烃类气体组成特征、成因及来源,并结合该区铀矿地质特征初步分析了烃类流体与砂岩型铀成矿关系。研究结果表明,直罗组下段砂体中CH_4及C_2+含量具有从含矿砂体、灰色砂体、灰绿-绿色砂体逐渐变小的分布特征,表明该区铀成矿与烃类气体关系密切。酸解烃中气体组成特征参数C_1/ΣC、C_1/C_2~+、C_2/iC_4、C_2/C_3、iC_4/nC_4、iC_5/nC_5、ln(C_1/C_2)、ln(C_2/C_3)及δ~(13) C_(CO_2)特征表明,中侏罗统直罗组下段砂岩层中烃类气体为有机成因的油型气,烃类气主要处于成熟—高成熟阶段,是原油裂解气与原油伴生气的混合气。通过气源对比分析认为,直罗组下段砂体中的烃类气主要来源于上三叠统延长组深湖—半深湖相腐泥型烃源岩。这些原油裂解气和原油伴生气的混合气主要沿深大断裂、微裂缝等其他运移通道向上运移到直罗组砂岩中,直罗组下段砂体褪色蚀变(漂白)和绿色蚀变均是深部逸散到该层位中的烃类气体对岩石发生蚀变作用的结果,靠近断裂的直罗组下段褪色蚀变砂岩与绿色蚀变砂岩之间的氧化-还原过渡带是该区砂岩型铀矿找矿的重点方向。  相似文献   

9.
<正>鄂尔多斯盆地分布着油、气、煤、铀等多种能源矿产,是进行有机-无机多种能源矿产相互作用研究的天然实验室。盆地北部分布着侏罗系直罗组下段大营—东胜大型砂岩型铀矿,铀矿富集区以南,分布着上古生界大气田;以北紧邻矿区分布着延安组顶部规模宏大的漂白砂岩以及乌兰格尔凸起上的白垩系油苗;目前找到的灰色砂岩型铀矿层受绿色蚀变砂岩控制;同时,在直罗组上段姜黄色砂岩中大规模遍布着碳酸盐蚀变产物"钙化木",在延安组漂白蚀变砂岩及直罗组含矿砂岩和绿色蚀变砂岩中还发育有碳酸盐胶结物。  相似文献   

10.
内蒙古东胜砂岩型铀矿后生成矿与油气关系   总被引:1,自引:1,他引:1  
发育于内蒙古鄂尔多斯盆地北部中侏罗统直罗组辫状河相杂砂岩体内的砂岩型铀矿,有一系列较为特殊的与放射性铀成矿有直接或间接关系的成矿地质现象:绿色化蚀变带、漂白退色化带、二次胶结钙化砂岩团块及钙化砂岩断续层与“钙化木”后生蚀变现象;在与铀矿化和与油气的关系认识上存在一定分歧。初步分析了它们的形成、成因及与铀成矿的关系及其找矿意义。  相似文献   

11.
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.  相似文献   

12.
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  相似文献   

13.
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.  相似文献   

14.
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.  相似文献   

15.
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.  相似文献   

16.
《Applied Geochemistry》2001,16(2):137-159
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).  相似文献   

17.
18.
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.  相似文献   

19.
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.  相似文献   

20.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号