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1.
西秦岭新生代高钾质玄武岩流体组成及其地幔动力学意义 总被引：5，自引：4，他引：1
西秦岭新生代高钾质玄武岩是认识大陆碰撞俯冲体制下地幔流体组成及深部动力学的岩石探针。本文采用分步加热质谱法测定了西秦岭高钾质玄武岩中斑晶及基质的流体化学组成和碳同位素组成,结果表明流体组分在200~400℃、400~800℃和800~1200℃阶段性释出,以H2O为主,其次为CO2和SO2,并含有相对较高的He含量。从橄榄石斑晶到斜长石斑晶和基质H2O和CO2逐步升高。橄榄石斑晶流体挥发份主要释气峰温度(900~1200℃)明显高于中国东部地幔捕虏体及其它地区超镁铁质岩体中的橄榄石,流体组份以SO2和CO2等氧化性组份为主,其CO2的δ13C值(-26.21‰~-20.85‰,平均-23.32‰)和CH4的δ13C值(-42.35‰~-38.17‰,平均-40.03‰)低于基质的δ13CCO2值(-16.43‰~-11.67‰,平均-13.22‰)和δ13CCH4值(-44.22‰~-34.03‰,平均-39.70‰)。基质中CO2和CH4碳同位素组成具有机质热裂解特征。原始岩浆的流体挥发份主要为SO2、N2和CO2,可能起源于较深的混杂地幔源区、演化于高fO2的环境。流体挥发份化学和同位素组成表明高钾质玄武岩浆挥发份中存在地幔和地壳来源组分,幔源岩浆上升演化过程中可能加入了大量的H2O和CO2等,可能存在碳酸岩岩浆的混合或岩浆穿透区域碳酸盐地层的混染;其中的再循环壳源组分可能为古特提斯洋闭合俯冲或其后华北克拉通与扬子克拉通碰撞相关的再循环壳源沉积物脱出的流体组分。 相似文献
2.
新疆库鲁克塔格地区兴地Ⅱ号镁铁-超镁铁质岩体的地球化学特征与岩石成因 总被引：1，自引：1，他引：0
兴地Ⅱ号镁铁-超镁铁质岩体位于塔里木盆地东北缘的库鲁克塔格地区,形态为不规则的漏斗状岩盆,出露面积约10km2。岩石类型主要有方辉橄榄岩、二辉橄榄岩、(含长)单辉橄榄岩、橄榄辉石岩、方辉辉石岩、二辉辉石岩、单辉辉石岩、橄榄辉长苏长岩、辉长苏长岩、橄榄辉长岩、辉长岩等,岩石类型属拉斑玄武岩系列。岩体的稀土元素含量低(∑REE=10.73×10-6~77.44×10-6),富集轻稀土元素(La/Yb)N=4.06~7.73和大离子亲石元素(Cs、Rb、Sr、Ba),亏损高场强元素尤其是Nb、Ta、Ti、P等,δEu为0.90~2.46多数岩石显示出正铕异常。岩相学及地球化学特征表明,岩浆运移过程中主要发生了橄榄石、斜方辉石、单斜辉石的分离结晶作用以及斜长石的聚集/堆晶。原生岩浆为富镁拉斑玄武岩,岩浆源区为富集型岩石圈地幔,岩浆上升侵位过程中局部遭受了陆壳的同化混染。兴地Ⅱ号岩体与金川岩体具有很多的相似之处,而且兴地Ⅱ号岩体已见有铜镍矿化。因此,兴地Ⅱ号岩体具有很好的找矿前景。 相似文献
3.
新疆喀拉通克镁铁质岩体群的岩石成因研究 总被引：19，自引：9，他引：10
喀拉通克镁铁质岩体群位于准噶尔板块北缘,由13个小岩体组成。主要岩石类型为方辉橄榄岩、橄榄苏长岩、辉长苏长岩、辉长岩、淡色辉长岩、辉长闪长岩等。主要造岩矿物为贵橄榄石、普通辉石、紫苏辉石、斜长石和数量较多的褐色普通角闪石、黑云母等。主量元素分属钙碱性系列、岛弧拉斑玄武岩系列和具有MORB属性的拉斑玄武岩系列。大多数样品具有高LREE/HREE比值、富集大离子亲石元素,相对亏损高场强元素（Nb、Ta、Ti）。εNd(t)=＋6.2~＋8.2,4件样品的εSr(t)=-0.6~-36.3,另有1件样品为+36.5;(206Pb/204Pb) i=17.784~18.008,(207Pb/204Pb) i=15.400~15.555,(208Pb/204Pb) i=36.973~37.560。元素地球化学和Nd、Sr、Pb、Os、O、S同位素体系证明,岩浆仅在局部遭受了同化混染作用。原生岩浆为高镁的拉斑玄武岩浆（MgO=11.6%）。岩浆在上侵和运移过程中经历了以单斜辉石为主的暗色矿物的广泛分离结晶作用和斜长石的凝聚,导致了淡色辉长岩的广泛分布和超镁铁岩的严重缺失。岩浆源区由被消减板片交代的地幔楔物质和软流圈地幔物质组成,因而富集不相容元素和水,并因交代作用与岩浆生成的时差短,而保持放射成因同位素的亏损状态。在岩石圈根部拆沉和软流圈地幔上涌过程中生成了喀拉通克镁铁质岩体群。 相似文献
4.
胶东早白垩世高镁闪长岩类的发现及其构造背景 总被引：3，自引：2，他引：1
胶东地区发育大规模早白垩世壳幔混合源花岗岩类，但一直未发现与花岗岩类相关的独立的幔源侵入体，给深入理解早白垩世壳幔演化带来了困惑。胶东的柳林庄和夏河城岩体以往被认为是三叠纪闪长岩类，本文在详细的野外地质工作基础上，通过年代学、岩石地球化学、同位素地球化学分析，发现这2个岩体为早白垩世高镁闪长岩。样品的SiO2含量在53.29%~62.54%之间，MgO含量为3.60%~8.10%，Mg#主要介于0.47~0.68之间；富集Ba、Rb、K等大离子亲石元素，亏损Nb、Ta、Zr等高场强元素；初始87Sr/86Sr值为0.7082~0.7083，与地幔平均值接近；εNd（t=113Ma）值很低（-20.5~-16.8），与胶东地区的基性脉岩同位素组成一致。2个岩体相比而言，柳林庄岩体富K2O、Fe2O3T，REE、LILE、HFSE含量较高，而MgO、Ni和Cr含量偏低。3件样品的锆石LA-ICP-MS U-Pb同位素加权平均年龄值分别为120.1±1.6Ma、118.3±1.7Ma和122.3±4.0Ma，与壳幔混合源的伟德山型花岗岩及胶东金矿的成岩、成矿时代一致，指示他们形成于统一的地球动力学背景。高镁闪长岩的地球化学特征介于高镁埃达克岩与赞岐岩及埃达克岩与Piip型高镁安山岩之间，指示其形成于古太平洋板块俯冲的地幔楔环境，为富集岩石圈地幔部分熔融的产物。夏河城岩体的岩浆直接来源于含角闪石的富集岩石圈地幔源区，而柳林庄岩体岩浆源区为含金云母的岩石圈地幔并且在岩浆上侵过程中混染了部分地壳物质。 相似文献
5.
扬子地块北缘周庵超镁铁质岩体矿物学特征及其对铜镍矿化的启示 总被引：2，自引：0，他引：2
扬子地块北缘~635 Ma周庵超镁铁质岩体是一个新发现的含铜镍硫化物矿化的隐伏岩体,主要由二辉橄榄岩组成。文章通过研究周庵岩体中橄榄石、铬铁矿和辉石的矿物成分变化探讨了岩浆演化过程和含矿岩体成因。根据岩石的矿物组合和蚀变程度,岩体从上到下分为3个部分:上部绿泥石-蛇纹石化二辉橄榄岩相带、中部二辉橄榄岩相带和下部绿泥石-角闪石化二辉橄榄岩相带。根据岩体中部带橄榄石和铬铁矿的成分,计算得到母岩浆的Mg#值为0.63,MgO/FeO摩尔比值为1.72,w(Al2O3)为10.2%~11.7%,w(Ni)为476×10-6,说明其为高镁玄武质岩浆;岩体中部带原生铬铁矿和粒间相铬铁矿核部的Cr2O3和Al2O3呈正相关关系,说明铬铁矿与粒间硅酸盐熔体发生了平衡交换,铬铁矿的高w(TiO2) 和Cr#值与拉张环境中层状岩体的铬铁矿特征一致;根据辉石温压计得到岩体中部单斜辉石和斜方辉石的共结温度为1 017~1 077℃,压力为(3.6~4.5)×108 Pa,暗示形成岩体的浅部岩浆房深度约为12 km。岩体上部和中部带的橄榄石Fo值大部分集中在80 mol%~85 mol%,w(Ni)介于2 255×10-6~4 455×10-6,说明这些橄榄石是从没有经过强烈分离结晶和硫化物熔离的岩浆中结晶出来的。岩体下部带橄榄石的Fo值(67 mol%~68 mol%)和w(Ni) (1 500×10-6~2 000×10-6)都低于岩体上部和中部带的橄榄石相应值,说明岩体下部带的橄榄石可能形成于演化程度较高、并经历了硫化物熔离的岩浆。因此,笔者认为周庵岩体是由相对原始的和演化了的高镁玄武质岩浆两期侵位形成的。 相似文献
6.
通过对出露在康古尔韧性剪切带西段的色尔特能超镁铁岩的野外地质调查和岩石学、岩石地球化学方面的分析研究工作,结果显示：色尔特能超镁铁岩发生了强烈蛇纹石化,基本蚀变成蛇纹岩;岩石主量元素具高Mg （w（MgO）=36.15%~37.96%）、高Cr （w（Cr2O3）=0.32%~0.36%）、高Ni （w（NiO）=0.17%~0.21%）、低Si （w（SiO2）=40.50%~41.92%）、贫Al （w（Al2O3）=1.19%~1.77%）、低Fe （w（TFeO）=6.98%~7.87%）特征,Mg#值为94.71~97.73,m/f值为8.03~9.42,属于典型镁质超镁铁岩,推测原岩为斜方辉石橄榄岩;稀土元素总量w（ΣREE）=1.44×10-6~2.92×10-6,配分模式为轻稀土微弱富集近平坦型,w（La）N/w（Yb）N=3.09~5.49,具一定程度的负Eu异常（δEu=0.48~1.09）和负Ce异常（δCe=0.53~0.60）;微量元素富集Ba、U、Ta,亏损Nb、Ti。色尔特能超镁铁岩属变质橄榄岩,是SSZ型蛇绿岩的底部组成单元,由原始地幔经2%~10%部分熔融形成的亏损地幔岩,其形成于俯冲带环境中的洋内弧后盆地。 相似文献
7.
华北克拉通北缘元古宙大庙Fe-Ti-P矿床的挥发份组成和C-H-O同位素研究 总被引：1，自引：1，他引：0
华北克拉通北缘~1.74Ga大庙斜长岩杂岩体赋含有大型Fe-Ti-P矿床。采用分步加热质谱法分别测定了块状Fe-Ti矿石、块状Fe-Ti-P矿石和浸染状矿石中磁铁矿、磷灰石和斜长石释出的挥发份组成、含量以及C-H-O同位素组成。依据矿物的释气总量变化特征将释气过程分为三个阶段:200~400℃、400~800℃和800~1200℃。根据不同类型矿石中矿物在不同释气阶段的挥发份组成、含量以及C-H-O同位素组成,可将含矿岩体中的流体类型分成四种:(1)斜长石800~1200℃阶段释出的变质流体,主要以H2O、N2+CO和CO2为主;(2)斜长石400~800℃阶段释出的幔源流体组分,主要以H2O、H2、CH4和CO2为主;(3)磁铁矿400~800℃阶段释出的地表流体,主要以H2O、CO2、SO2和H2S为主;(4)所有矿物200~400℃阶段释出的代表后期次生包裹体的组分,以H2O和CO2为主。矿石中的磁铁矿相对富集H2O和CO2等流体组分,是在相对氧化的条件下结晶的;而斜长石释出气体中H2和CH4的含量较高,是在相对还原的环境中结晶的。这反映出斜长石可能是在岩浆早期相对还原的条件下结晶的,而磁铁矿是在岩浆演化晚期相对氧化的条件下结晶的,这一过程的转变可能与岩浆演化晚期,岩浆中的挥发份逐渐聚集以及地表流体的加入有关。岩浆中H2O和CO2等流体含量的不断增加导致岩浆的氧逸度逐渐升高,最终造成磁铁矿的大量结晶并富集成矿。 相似文献
8.
根据开放体系条件下的瑞利分馏原理,并考虑岩浆中可能溶解的合碳和含硫组分,从理论上定量模式了岩浆去气作用对火成岩碳、硫同位素组成的影响。结果表明,岩浆CO2去气作用能够导致岩石中碳酸盐显着亏损13C,其δ13C值能够从原始-5‰变化到-20‰(PDB);岩浆CH4去气作用则导致岩石中碳酸盐相对富集13C,其δ13C值能够从原始-5‰变化到+4‰。岩浆SO2去气作用可以导致岩石中硫化物显着亏损34S,其δ34S值能够从0‰变化到-8‰(CDT);岩浆H2S去气作用则导致岩石中的硫化物相对富集4S,其δ34S值能够从0‰变化到+6‰。因此,除源岩原始同位素不均一性和地壳物质混染能引起火成岩的碳、硫同位素组成发生较大变化外,岩浆去气作用也是重要原因之一。 相似文献
9.
天宇铜镍矿床的岩相学、锆石U-Pb年代学、地球化学特征：对东疆镁铁-超镁铁质岩体源区和成因的制约 总被引：24，自引：13，他引：11
天宇镁铁-超镁铁质岩体位于新疆中天山地块与觉罗塔格构造带的分界断裂——沙泉子深大断裂的南侧约5km。岩体呈向北陡倾的岩墙状,地表出露面积约0.056km2。该杂岩体主要由辉长岩、辉石岩、辉橄岩和橄榄岩相组成,橄辉岩、辉橄岩和橄榄岩是主要的Cu、Ni赋矿岩相。镁铁-超镁铁岩的主量元素含量显示,天宇岩体属拉斑玄武岩成因系列,m/f为1.44~3.61,平均值为2.25,为铁质超基性岩（m/f=2~6.5）。稀土元素标准化配分模式为轻稀土富集型,Eu弱负异常或无异常,相似的稀土元素配分模式说明岩体的同源性。富集大离子亲石元素,亏损高场强元素Nb、Ta,说明源区可能有陆壳物质的混染。Nb/Hf、Ce/Pb、Nb/U、La/Sm、Th/Nb比值显示岩体可能经受上地壳物质的混染。锆石的LA-ICP-MS U-Pb年代学研究表明,岩体形成年龄为290.2±3.4Ma,与东天山地区镁铁-超镁铁质杂岩体的形成时间一致。锆石的Lu/Hf比值比较均一,且(176Hf/177Hf) i变化很小,说明源区性质比较单一。锆石的(176Hf/177Hf) i值为0.282625~0.282770,相应的εHf(t)均为正值（1.10~6.06）,Lu-Hf的单阶段模式年龄（tDM1）为674~884.7Ma,平均年龄为799Ma,比岩体的U-Pb年龄大,显示岩浆来源于亏损地幔或者源区有壳源物质的加入。上述岩石地球化学、年代学特征,为晚古生代古亚洲洋向南俯冲提供了佐证。 相似文献
10.
新疆坡北镁铁-超镁铁质杂岩体由一个辉长岩体以及二十多个超镁铁质侵入体组成,其中坡一超镁铁质岩体稀有气体同位素组成揭示存在地幔柱的贡献。坡北杂岩体西端的坡一、坡四、坡十和坡十四等几个超镁铁质岩体的稀有气体同位素对比分析结果表明,岩浆矿物的3He/4He值（0.26~2.79Ra）分布于地壳与地幔值之间,较高的20Ne/22Ne和较低的21Ne/22Ne值分布于Ne质量分馏线（MFL）和L-K线之间,40Ar/36Ar=295~598。3He/4He与40Ar/36Ar比值揭示坡北杂岩体西端不同超镁铁质岩体形成过程中地幔（柱）、地壳和大气组分的贡献不同,岩体成因也可能不同。其中,坡一岩体具有地幔柱作用的贡献,其他三个岩体的岩石圈地幔及地壳流体组分的贡献较大。岩浆地幔源区由深部地幔柱物质叠加俯冲流体交代的岩石圈地幔物质所组成,大气与地壳物质组分可能由俯冲再循环洋壳带入到岩浆地幔源区以及围岩物质的混入。 相似文献
11.
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
12.
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
13.
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
14.
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
15.
《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
16.
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
17.
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19.
《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
20.
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