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新开岭－科洛杂岩位于中国东北地区的嫩江－黑河构造带中,其变形规律与成因一直是制约东北地区乃至邻区构造演化的关键问题之一.据详尽的野外调查,系统分析了岩石宏观糜棱面理、矿物拉伸线理、“A”型褶皱、不对称褶皱、眼球状旋转构造和显微书斜式、眼球状旋转等构造样式.构造解析及运动学分析反映杂岩带两侧整体分别向NW及SE向的伸展滑脱特征;杂岩带内黑云斜长片麻岩及侵入糜棱岩中的闪长玢岩锆石U-Pb（LA-ICP-MS）定年及区域对比研究结果显示,其韧性变形变质作用时代为中侏罗世（167 Ma）,变质峰期时限为170~163 Ma,中侏罗世晚期（163 Ma）暴露于地表.新开岭－科洛杂岩具上盘盖层、拆离韧性剪切带及下盘核杂岩3层式结构特征.核内为大面积分布的花岗岩类,地层时代远比核外地层偏新,并无“古老”的变质岩;拆离韧性剪切带变形温度约400~500℃,其变质强度达绿片岩相,后期发生明显退变质作用.新开岭－科洛岩浆核杂岩主要是在岩浆底侵、花岗岩岩体强力侵位引起地壳隆升的伸展构造背景下形成. 相似文献
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科洛杂岩出露于黑龙江省嫩江县大兴安岭北段,构造解析指示其为一大型伸展滑脱构造,整体反映杂岩体向南东伸展滑脱的特征。依据杂岩体显微构造特征,推测科洛地区伸展滑脱变形带变形温度约为300～450 ℃。滑脱带中变形花岗片麻岩样品中黑云母单矿物的 40Ar/39Ar 年龄为118.39～117.37 Ma,指示伸展滑脱带形成时代为早白垩世晚期。结合大兴安岭地区中生代岩浆活动特征和南北变质核杂岩对比研究,认为大兴安岭整体经历了早白垩世中晚期的快速隆升,形成一系列变质核杂岩,发育大规模伸展变形作用,与松辽盆地坳陷期具有良好的耦合关系。 相似文献
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黑龙江科洛杂岩变形特征、阶段和意义 总被引：1，自引：0，他引：1
兴蒙造山区东段的科洛地区,自古亚洲洋关闭之后,经历了复杂的多阶段陆内变形,每一期变形都具有不同的机制,均是中国东北中生代以来板块边缘重要构造事件的反映。三叠纪中晚期,科洛杂岩经历了上盘指向NNE方向的韧性挤压变形,相关变形分布在整个科洛杂岩地区,大量低角度石英拉伸线理以及A型褶皱枢纽均指示了松嫩地块NNE向的运动,科洛杂岩也在此时形成。科洛杂岩并不是松嫩地块的基底,而是中生代构造事件的变质产物,该期事件不是古亚洲洋关闭后的造山带伸展,而与来自东侧和南侧的挤压有关。晚侏罗世-早白垩世科洛地区左行韧性走滑是蒙古-鄂霍茨克洋的关闭所致,其变形集中在科洛杂岩的西部边界剪切带上。白垩纪时科洛杂岩受到伸展构造的改造,以一系列向南东倒伏、走向NNE-SSW的相似褶皱为特征,褶皱的倒伏向不随位置的变化而改变,其伸展不是典型的变质核杂岩。新生代科洛杂岩又受到了近SN向的挤压,发生区域性的宽缓褶皱变形。 相似文献
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大兴安岭北段伸展构造 总被引：4，自引：0，他引：4
本文对大兴安岭北段额尔古纳七卡地区发育的大型区域伸展滑脱构造开展了详细的研究,并系统地总结讨论了大兴安岭地区伸展构造及其与大兴安岭隆升的成因联系。查明七卡伸展构造带总体走向NE,滑脱面倾向NW,变形为具有减薄特征的简单剪切应变,发育SL构造岩,运动指向标志J显示向NW的伸展滑脱。结合区域上嫩江科洛伸展构造、嘎啦山伸展构造和磋岗伸展构造的对比研究表明,大兴安岭地区的伸展构造应该是区域伸展作用的产物,形成时间为早白垩世。随着大规模区域伸展作用,大兴安岭地区发生强烈的岩浆底侵,导致大兴安岭快速隆升,从而使其形成东侧向SE和西侧向NW方向滑脱的伸展构造。 相似文献
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四川石棉—冕宁地区之伸展构造 总被引：5，自引：0，他引：5
研究区在中生代造山过程中,以穹隆状变形变质体发育为特征。可分为岩浆核杂岩和变质核杂岩。前者位于地槽区,具前造山期隆－滑构造变形、造山期和后造山期的收缩及伸展变形的演化,与碲矿关系密切;后者位于地台区,经历了伸展滑脱、逆冲－推覆和平移剪切变形过程,对区内金矿的形成、分布起重要控制作用。 相似文献
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对于喀喇沁变质核杂岩早白垩世构造过程与形成模式长期以来存在着不同的认识。通过详细的野外构造观察及擦痕应力场反演,并结合前人年代学数据,有效地制约了喀喇沁变质核杂岩早白垩世的构造演化,并对其形成模式进行了分析。结果表明,起源于晚侏罗世的喀喇沁变质核杂岩,在早白垩世(141～100 Ma)再次经历了强烈的伸展与岩浆活动。在此伸展活动中,沿着核部杂岩两侧分别发育了NE走向、倾向相反的楼子店-八里罕和上店-东风大型正断层,进而控制两侧半地堑式的小牛与平庄盆地的发育。在这两条边界断层的伸展运动及随后的均衡隆升中,核部杂岩不断抬升与剥露,先后发育了NE-NNE向的伸展韧性变形带与脆性正断层。这些早白垩世韧性和脆性伸展构造一致指示拉张方向为NW-SE向。综合分析表明,区内早白垩世伸展活动经历了141～134 Ma的初始伸展与同构造岩体侵位阶段、133～126 Ma的边界断层强烈活动与核部快速抬升阶段以及125～100Ma的均衡隆升阶段。喀喇沁变质核杂岩在早白垩世的伸展活动中转变为地垒式伸展穹窿,其强烈伸展活动出现在华北克拉通破坏峰期,动力学背景是古太平洋板块俯冲导致的远场弧后拉张。 相似文献
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变质核杂岩与岩浆作用成因关系综述 总被引：12，自引：0，他引：12
对岩浆与伸展作用的关系、伸展作用中岩浆的成因和需加强的工作进行了讨论,并重点论述了变质核杂岩形成机制与侵入作用的关系。在造山带重力势能差和深部作用等各种因素导致的拉伸应力场作用下,岩石圈地幔和地壳通过减压或深部热活动发生部分熔融而形成岩浆,岩浆的上涌强化了地壳伸展,对地壳的弱化作用触发伸展构造的发生。岩浆作用是变质核杂岩形成的主导因素之一,其主要包括对地壳的加热、弱化导致拆离断层的形成及由其浮力和密度产生不均一隆升而形成穹隆。 相似文献
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核杂岩顶部代表深处韧性变形的长英质糜棱岩,其实是温度敏感型的,在异常高的古地温梯度或同构造岩浆活动的情况下,不一定代表中地壳变形的产物.伸展的剥离断层造成相当厚的地壳柱的切失,但在长期受剥蚀的古老岩系出露处,年轻岩层(如白垩系或第三系)直接覆盖于太古宇之上,究竟是沉积缺失还是构造切失,必须加以具体分析.核杂岩隆升至地面,难以单纯用地壳变薄的重力均衡作用来解释.与变质核杂岩密切相关的局部的古地热异常、同构造岩浆岩的强力侵位等,揭示出热隆和岩浆作用在核杂岩隆升中的重要作用,以及变质核杂岩和岩浆核杂岩的密切相关;二者可能只是表现形式不同而已.晚造山的伸展不一定是变质核杂岩所反映的伸展作用的唯一起因.一个地区可以有多次伸缩交替的构造运动. 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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Mercury,arsenic, antimony,and selenium contents of sediment from the Kuskokwim River,Bethel, Alaska,USA 总被引：1，自引：0，他引：1
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
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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