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1.
通过对宽甸新生代碱性玄武岩、地幔包体及辉石巨晶的稀有气体同位素组成的分析，认为不同岩性稀有气体含量的差异反映了岩浆作用过程中轻、重稀有气体的分馏特性，较轻的稀有气体(He、Ne)比较重的稀有气体(Kr、xe)具有更高的活动性和不相容性；该地区上地幔源区具有典型的MORB型源区特征，以辉石巨晶为代表；地幔包体的^3He／^4He值较低，可能是地幔流体交代作用造成的；大陆碱性玄武岩具有与大洋玄武岩截然不同的He同位素组成，反映了大陆区地幔岩浆上升过程中受到了陆壳物质混染。地幔源区^40Ar／^36Ar值为350左右，二辉橄榄岩和碱性火山岩的^40Ar／^36Ar值比大气略高，可能有大气组分的混合。部分样品中有^21Ne、^22Ne、^129Xe、^134Xe和^136Xe相对于大气的过剩现象，是核成因造成的。 相似文献
2.
辽宁宽甸新生代火山岩和地幔包体He-Ar同位素组成 总被引：8，自引：1，他引：8
宽甸新生代碱性玄武岩、地幔包体及辉石巨晶的稀有气体同位素组成和流体含量分析表明，不同岩性稀有气体含量的差异反映了岩浆作用过程中轻、重稀有气体的分馏特性，较轻的稀有气体(He、Ne)比较重的稀有气体(Kr、Xe)具有更高的活动性和不相容性；该地区上地幔源区具有典型的MORB型源区特征，以辉石巨晶为代表；地幔包体的3^He／^4He值较低，可能与地幔上隆过程中富集地幔流体的交代作用或地幔塑性变形作用丢失了部分原始He有关；大陆碱性玄武岩具有与大洋玄武岩截然不同的He同位素组成，反映了大陆区地幔岩浆上升过程中受到了陆壳物质混染。地幔源区^40Ar／^36Ar值为350左右，二辉橄榄岩和碱性火山岩的^40Ar／^36Ar值比大气略高，可能有大气组分的混入。部分样品中有^21Ne、^22Ne、^129Xe、^134Xe和^136Xe相对于大气的过剩现象。 相似文献
3.
河北汉诺坝新生代玄武岩中幔源包体和高压巨晶的氦同位素地球化学研究 总被引：3，自引：0，他引：3
对该地区新生代玄武岩中幔源包体和高压巨晶的氦同位素进行了初步研究。幔源包体中橄榄石的3 He 4 He值为 (0 .15～ 7.4)× 10 - 6,较MORB值明显偏低 ,甚至低于大气的值 ,说明该地区曾发生过强烈的地幔交代作用。高压巨晶辉石和石榴子石的氦同位素组成与此明显不同 ,其3 He 4 He值为 (5 .7～ 2 4.3)× 10 - 6。提出幔源包体和高压巨晶不是同源的 ,二者可能与寄主玄武岩均无必然成因联系。在汉诺坝地区一件石榴子石巨晶中还发现了异常高的3 He 4 He值。 相似文献
4.
利用地幔柱、上地幔和地壳在稀有气体同位素组成方面的明显差异,国际上在对地幔柱进行示踪和判识方面已取得了良好的效果。地幔柱的3He/4He值大于8～8.5Ra(Ra=1.4×10-6),且高于上地幔和地壳值;地幔柱的20Ne/22Ne值大于等于10.8,与上地幔值接近,但地幔柱的21Ne/22Ne值低于上地幔值;地幔柱的40Ar/36Ar值一般明显低于上地幔值;地幔柱的129Xe/130Xe和136Xe/130Xe值普遍高于上地幔和地壳值,且高于上地幔值约10%以上。中国东部新生代地幔岩的3He/4He值总体在上地幔3He/4He端员值(8±1Ra)的上下变化,与地幔柱的3He/4He值差异较大。大火成岩省(LIP)的形成与深部地幔柱的活动有关,峨眉山玄武岩是中国目前唯一被学术界普遍认可的LIP。开展包括峨眉山玄武岩在内的有关地幔柱稀有气体同位素示踪方面的研究,对于深化中国地幔柱领域的研究和推动大陆动力学研究的进程具有重要意义。 相似文献
5.
应用热爆裂质谱测量和高温熔融样品释气技术分别测定了山旺、栖霞和鹤壁新生代玄武岩中橄榄岩捕虏体中的橄榄石颗粒的流体和稀有气体组成。结果表明,鹤壁方辉橄榄岩具低于大气的~3He/~4He 比值0.778Ra 和大气成因的 Ne、Ar、Kr、Xe 组成。三个地区饱满地幔样品均以还原性流体为主,CO_2/~3He、N_2/~3He、N_2/Ar 比值分别为(0.62～4144)×10~9、(2631～64482)×10~6、269～73467。这些还原型流体偏离典型的幔源流体组成而表现出明显的碳和氮元素过剩,具有大气-地幔-壳源组份混合的特点,反映了大气和富含有机质的壳源组份在新生岩石圈上地幔中的影响。同时,这些饱满地幔样品的 Ne、Ar、Kr、Xe 具有大气属性,反映了大气型稀有气体在上地幔源区的广泛混染。其中,山旺和栖霞的~3He/~4He 比值分别为(2.91～3.07)Ra、(1.79～4.01)Ra,均高于大气低于 MORB,具有交代富集地幔的特点,而鹤壁则具有类似 MORB 的~3He/~4He 比值(7.03～7.05)Ra。这样的流体和稀有气体组成差别显示华北东部新生岩石圈地幔具亏损 MORB 型的特点并含壳源组份, 且其东缘所含壳源组份比例高于中部,说明华北东部新生岩石圈地幔中有俯冲洋壳组份的记录。 相似文献
6.
稀有气体被广泛用作地球化学示踪剂,本文对塔里木大火成岩省西北缘瓦吉里塔格霞石岩中的橄榄石和辉石单矿物进行了稀有气体同位素测定。结果表明,瓦吉里塔格霞石岩中的橄榄石和辉石单矿物具有较低的~3He/~4He值(分别为2.0~2.4 Ra和0.65~0.85 Ra)和略高于大气值的~(40)Ar/~(36)Ar值(342.3~651.7),反映了由古板块俯冲导致的较低的He、Ar同位素比值特征。研究表明,早中古生代南天山洋向南俯冲到塔里木板块之下,将富U或富~4He以及含有大气组分的流体带入到深部地幔,在塔里木地幔柱的作用下地幔源区发生低程度部分熔融产生霞石岩岩浆。 相似文献
7.
岩矿样品中稀有气体同位素组成的质谱分析 总被引：44，自引：0，他引：44
利用MM5400质谱计建立了岩矿样品中He,Ne,Ar,Kr和Xe同位素组成的测定方法。仪器的工作状态稳定，且能将3He与HD的谱峰完全分开。在处理气体将非稀有气体尤其是碳的化合物用海绵钛炉充分消除，在测试Ne同位素组成时用烧结型不锈钢滤芯可以基本消除40Ar^2 对20Ne的干扰，必要时要进行校正；为了保证谱峰强度与相应元素量的大小之间的线性关系，质谱计主机中的气体量应控制合适，对宽甸新生代火山岩及地幔岩包体中稀有气体同位素组成的测定结果表明，中国东部上地幔具有大洋中脊玄武岩（MORB）型的源区特征。 相似文献
8.
稀有气体同位素在示踪成矿作用流体来源方面具有独特优势。本文应用熔融质谱法测定了金川Cu-Ni-PGE硫化物矿床23个硅酸盐矿物和金属硫化物单矿物的He、Ne和Ar丰度和同位素组成。结果表明,硅酸盐矿物的3He/4He比值(0.239Ra)略低于硫化物(平均0.456Ra),且从橄榄石(平均0.291Ra)、斜方辉石(0.215Ra)到单斜辉石(0.174Ra)逐渐降低,20Ne/22Ne-21Ne/22Ne分布于MORB与大陆地壳演化线之间,扣除放射性成因4He*和40Ar*后橄榄石和辉石中3He/4He和40Ar/36Ar接近岩石圈地幔组成。He、Ne和Ar同位素组成示踪表明成矿岩浆中存在岩石圈地幔(SCLM)、地壳(CC)和大气饱和流体(ASW)三种端元成分,硫化物熔体的分离发生在岩浆结晶分异的早期。岩石圈地幔部分熔融形成的成矿初始岩浆经历了两阶段的演化。在深部岩浆房高温成矿岩浆同化围岩引入地壳混染组分,促使硫饱和及硫化物熔体的熔离,同时形成具有壳幔混合特征的混合岩浆组分(MC),上升至上部岩浆房后混入较高比例的大气饱和流体,进一步促使硫饱和及浸染状硫化物就地熔离堆积。 相似文献
9.
雅鲁藏布江蛇绿岩中地幔柱型岩浆作用——来自氦、氩同位素的证据 总被引：11，自引：1，他引：11
雅鲁藏布江蛇绿岩的氦、氩同位素组成分别是：蛇绿岩中变质橄榄岩的^3He/^4He比值为1．104-3．384Ra，平均为2．383Ra；玄武岩的He同位素组成比较均一，^3He/^4He平均值为5．359 Ra；辉绿岩的^3He／^4He比值变化较大，为1—5Ra。由于各岩石样品有不同程度的蚀变，造成放射性成因He的加入，因此大多数样品He同位素组成比低于亏损地幔大洋中脊玄武岩的值(MORB≈8Ra)，不能真实反映源区特征。而采自吉定的辉绿岩样品^3He/^4He比值平均高达31．57Ra，与夏威夷发现的热点地幔源区的样品比值接近；分步加热法进一步测试，其高比值的He是在低温区段释放的。这种高^3He/^4He比值He的捕获，表明雅鲁藏布江蛇绿岩形成时存在地幔柱型富集地幔岩浆作用。 相似文献
10.
广东麒麟绿钙闪石巨晶的地球化学特征 总被引：1，自引：0，他引：1
本文对罕见的幔源绿钙闪石巨晶进行了综合的地球化学分析，主要元素，稀土微量元素和Ｓｒ，Ｎｄ同位素的特征表明；绿钙闪石巨晶是碱性玄武岩浆在地幔条件下的结晶产物；相对于寄主玄武岩，绿钙闪石巨晶均属捕虏晶，它们与共存的橄榄岩包体无成因联系，其形成可能与共存的黑色包体有关。 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
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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
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