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1.
新疆且末县江尕勒萨依村杨叶组首次发现了大量孢粉化石。经鉴定共计37属81种,根据孢粉化石组合特征及地层分布将其命名为Cyathidites-Neoraistrickia-Disacciatrileti组合,时代为中侏罗世早期,与西北区、华北区同时代地层中孢粉组合可以很好的对比。通过研究孢粉组分与母本植物的亲缘关系,得出中侏罗世早期江尕勒萨依地区植被主要由真蕨类植物、石松类植物和乔木的松柏类及苏铁类组成,反映古气候为热带-亚热带湿润气候。 相似文献
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吐鲁番—哈密盆地托克逊凹陷早侏罗世地层中产孢粉化石共53属74种。通过对纵向上典型属种及优势组分含量变化规律的分析可划分为两个孢粉组合：Osmundacidites-Protopinus-Cycadopites组合和Cyathidites-Piceaepollenites-Cycadopites组合，它们分别产自八道湾组和三工河组。根据孢粉组合特征及与国内外有关化石群进行比较，八道湾组的时代应属早侏罗世早期；三工河组的时代应为早侏罗世晚期。托克逊地区当时的植被是由银杏、苏铁类和松柏类等乔木．并伴有真蕨类等草本植物组成。古气候应属亚热带气候。 相似文献
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北黄海东部坳陷的太阳区块富含中生代孢子、花粉化石。根据化石属种与含量的变化,自下而上划分出三个孢粉组合:即中侏罗世晚期(Bathonian-Callovian)的Cyathidites-Cycadopites-Quadraeculina组合,晚侏罗世的Classopollis-Protopinus-Callialasporites组合和早白垩世早、中期的Lygodiumsporites-CicatricosisporitesSchizaeoisporites组合。孢粉化石研究证实北黄海东部坳陷存在中侏罗世地层。 相似文献
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新疆乌恰县莎里塔什组生物地层新知 总被引：2，自引：0，他引：2
对新疆乌恰县塔塔村下侏罗统莎里塔什组孢粉植物群的研究，共发现孢粉２２属２６种，植物化石１２属１５种。根据这些孢粉化石建立了一个孢粉组合，命名为Ｃｙａｔｈｉｄｉｔｅｓ－Ｃｌａｓｓｏｐｏｌｌｉｓ组合，再根据侏罗纪的标志植物锥叶蕨（Ｃｏｎｉｏｐｔｅｒｉｓ）的存在，将莎里塔什组的时代确定为早侏罗世，为乌恰地区早侏罗世生物地层提供了可靠依据 相似文献
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通过对大兴安岭中南部宝日勿苏地区地质调查井宝D1井井深22~255.70m井段发现的孢粉化石的系统分析研究,共获得孢粉化石47属65种（包括未定种）.根据孢粉化石属种类型及其含量和变化特征,将孢粉化石组合划为Lycopodiacidites-Densoisporites-Piceaepollenites组合,时代为早白垩世早期,孢粉化石赋存地层相当于白音高老组.通过系统分析孢粉组合中主要孢粉属种及其母体植物的生长环境,推测大兴安岭中南部地区在早白垩世早期为暖温带-亚热带气候条件.同时旱生植物的大量出现,表明该区在早白垩世早期受到了干旱气候的影响,但与典型的干旱环境不同,推断与当时的火山活动有关. 相似文献
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新疆吐哈盆地连木沁构造带,在连4-S井4215～4832m取样分析,该地层孢粉化石数量和属种较多,主要为苔癣、蕨类植物孢粉和裸子植物花粉,孢粉化石组合具有较清楚的时代地层意义,通过分析命名为Aratnspontes - Punctatispozites - Colpectopollis组合。根据组合主要分子的时限及其含量变化,以及与有关已知时代孢粉组合进行比对,可确认该地层地质时代为克拉玛依组。 相似文献
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辽宁北部秀水盆地秀D1井孢粉组合及其地层意义 总被引：2，自引：1，他引：1
孢粉化石采自辽宁省北部秀水盆地的秀D1井,分析、鉴定和系统研究结果表明,来自秀D1井井深62.1~1089.7m的孢粉化石自下而上划分为3个孢粉组合,下部孢粉组合(井深703.85~1089.7m)以Osmundacidites-Klukisporites-Podocarpidites为代表,地质时代为晚侏罗世堤塘期(Tithonian),中部孢粉组合(井深381.5~699.3m)以Densoisporites-Cicatricosisporites-Piceaepollenites为代表,地质时代为早白垩世贝里阿斯期(Berriassian),上部孢粉组合(井深62.1~339m)以Cicatricosisporites-Impardecispora-Pinuspollenites为代表,地质时代为早白垩世凡兰吟期—欧特里夫期(Valanginian-Hauterivian)。秀D1井钻遇地层所含孢粉组合特征在区域上可以与冀北地区大北沟组,辽宁西部地区下白垩统义县组、九佛堂组,松辽盆地东南缘下白垩统火石岭组、沙河子组所产的孢粉组合对比。含孢粉组合地层时代的确定解决了井柱地层的划分,以及与区域地层的对比关系,同时为区域地层古生物研究提供了翔实的基础资料。 相似文献
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甘肃靖远王家山含煤盆地位于北祁连东部,系一内陆山间盆地,区内中侏罗世地层发育,层序清楚,所合孢粉化石丰富,共得61属,93种。对其孢粉组合的研究有利于我国北方各个互不相连的侏罗纪盆地的地层对比,进而有助于深入研究侏罗纪古地理、古气候,并对探索成层矿床的找矿规律有所帮助。 相似文献
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在北羌塘盆地胜利河地区原侏罗系中上统采集到丰富的孢粉化石,该孢粉化石组合以Classopollis、Cyathidites、Osmundacidites及Brevilaesuraspora占主要趋势,经研究及区域对比孢子花粉化石组合时代为中-晚侏罗世。该时期孢粉组合指示的古植被特征以喜干热的掌鳞杉科(Chriolepidaceae)为优势类群,还有少数苏铁科、南美杉科、松科、杉科、松柏科、罗汉松科等植物伴生其间,林下生长着类型多样的蕨类植物。因此,本孢粉植物群反映的古气候属于干旱炎热的热带-亚热带。 相似文献
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E. M. Prasolov S. A. Sergeev B. V. Belyatsky E. S. Bogomolov K. A. Gruzdov I. N. Kapitonov R. Sh. Krymsky V. O. Khalenev 《Geochemistry International》2018,56(1):46-64
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
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奥地利安东帕有限公司 《岩矿测试》2009,28(3):306-306
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
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S. Viswanathan K. Surya Prakash Rao B. Mahabaleswar 《Journal of the Geological Society of India》2013,82(6):621-627
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
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《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
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S. M. Moosavirad J. Rasouli M. R. Janardhana M. R. Moghadam M. Shankara 《Arabian Journal of Geosciences》2013,6(10):3623-3634
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
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《Chemical Geology》2007,236(1-2):13-26
We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO2. 相似文献
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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