丹宁棉分离富集—发射光谱法同时测定地质样品中微量铌钽锆铪

采用丹宁棉对地质样品溶液中的铌、钽、锆、铪进行分离富集，将写信后的丹宁棉在600℃灼烧30min，灰分用发射光谱法同时测定四元素。检出限与通常的发射光谱法相比降低约2个数量级，经国家级标准物质检验，结果与标准值相符，精密度试验，各元素的RSD（n＝20）为2.6％－7.9％。     

Determination of Zirconium, Niobium, Hafnium and Tantalum at ng g-1 Levels in Geological Materials by Direct Nebulisation of Sample HF Solution into FI-ICP-MS

We have developed a rapid and accurate method to determine Zr, Nb, Hf and Ta (denoted as HFSE) in geological samples by inductively coupled plasma-mass spectrometry fitted with a flow injection system (FI-ICP-MS). The method involves sample decomposition by HF followed by HF dissolution of HFSE coprecipitated with insoluble M and Ca fluoride residues formed during the initial HF attack. This HF solution was directly nebulized into an ICP mass spectrometer. An external calibration curve method and an isotope dilution method (ID) were applied for the determination of Nb and Ta, and of Zr and Hf, respectively. Recovery yields of HFSE were > 96% for peridotite, basalt and andesite compositions, apart from Zr and Hf for peridotite (> 85%). No matrix effects for either signal intensities of HFSE or isotope ratios of Zr and Hf were observed in basalt, andesite and peridotite solutions down to a dilution factor of 100. Detection limits in silicate rocks were 40, 2, 1 and 0.1 ng g-1 for Zr, Nb, Hf and Ta, respectively. This technique required only 0.1 ml of sample solution, and thus is suitable for analysing small and/or precious samples such as meteorites, mantle peridotites and their mineral separates. We also present newly determined data for the Zr, Nb, Hf and Ta concentrations in USGS silicate reference materials DTS-1, PCC-1, BCR-1, BHVO-1 and AGV-1, GSJ reference materials JB-1, -2, -3, JA-1, -2 and -3, and the Smithsonian reference Allende powder.     

佛冈高分异I型花岗岩的成因:来自Nb-Ta-Zr-Hf等元素的制约

华南南岭地区发育有大面积的与钨锡成矿相关的侏罗纪花岗岩,然而其中有些花岗岩的成因类型却难以确定。本文以佛冈岩体为例,结合前人已发表数据,对佛冈花岗岩体中Nb、Ta、Zr和Hf等元素的迁移特征及其原理进行探讨,并对佛冈花岗岩的成因类型进行了厘定。随着分异程度增加,佛冈花岗岩Nb和Ta含量增加,Nb/Ta(3.6~15.3)和Zr/Hf(17.3~38.9)比值降低并发生分异。随着Zr含量的降低,佛冈花岗岩的Zr/Hf比值降低,这一特征表明锆石的分离结晶作用使得佛冈花岗岩的Zr/Hf比值分异。Nb/Ta比值分异可能与角闪石和黑云母的分离结晶作用有关。随着Nb/Ta比值降低,Y/Ho比值增加,这一特征表明佛冈花岗岩Nb/Ta比值的分异也和岩浆演化后期的流体有关。佛冈花岗岩不含原生的富铝矿物,为准铝质到弱过铝质岩石。随着分异程度增加,佛冈花岗岩P2O5含量降低,表明它不是S型花岗岩。随着Y/Ho比值增加和Nb/Ta和Zr/Hf比值降低,佛岗花岗岩Ga/Al和Fe OT/Mg O比值增加,从典型I型花岗岩特征演化到类似A型花岗岩的地球化学特征。因此,我们认为佛冈花岗岩不是A型花岗岩而是高分异的I型花岗岩。区域上与成矿相关的流体和花岗质岩浆的相互作用和分离结晶作用,使得华南南岭地区的花岗岩地球化学特征复杂,所以其成因类型也变的难以确定。     

Constraints from eclogite and MARID xenoliths on origins of mantle Zr/Hf–Nb/Ta variability

New trace-element data of rutile in kimberlite-borne ~1.85 Ga eclogite and pyroxenite xenoliths from the central Slave craton, as well as ~110 Ma MARID xenoliths from the Kaapvaal craton, provide constraints on the origins of lithospheric and sublithospheric mantle variability in high field strength element ratios. Rutiles in eclogites and pyroxenites have Zr/Hf ranging from 20 to 62 and Nb/Ta ranging from 10 to 40. Rutiles in MARID xenoliths have Zr/Hf from 24 to 33 and Nb/Ta from 10 to 41. Calculated whole-rock Zr/Hf is suprachondritic for eclogites with suggested gabbroic protoliths and subchondritic for boninite-like eclogites; the latter is consistent with cpx-controlled depletion in the protolith source. Within each eclogite type, positive correlations of Zr/Hf with La/Lu and negative correlations with Lu/Hf likely reflect fractionation of cpx and/or plagioclase during crystallisation of the protoliths. Zr/Hf–Nb/Ta relationships of some MARID-type rocks, which are products of lithospheric mantle metasomatism, and eclogite xenoliths plot on a silicate differentiation trend, whereas other samples have higher Nb/Ta at a given Zr/Hf. Fractionation of a few percent rutile from an HFSE-rich mafic melt can generate a trend towards strongly increased Nb/Ta at minimally changed Zr/Hf in the residual melt. Superposition of rutile fractionation on the effects of silicate differentiation, which fractionates Zr/Hf more strongly than Nb/Ta, can explain the Zr/Hf–Nb/Ta relationships of most eclogites from the central Slave craton as well as those of MARID rocks, metasomatised peridotites and group II kimberlites. By contrast, Zr/Hf–Nb/Ta relationships suggest that Group I kimberlites are mixtures between depleted peridotite and carbonatite. Thus, high Nb/Ta is a signature of lithospheric processes and may not be important in deeply subducted eclogites that bypass extended residence in the lithosphere. Conversely, considerable primary Zr/Hf variability was inherited by the eclogites, which is indicative of the compositional diversity of ancient subducted oceanic crust, which is expected to have generated substantial heterogeneity in sublithospheric basalt sources.     

Geochemistry and Radioactive Potentiality of Um Naggat Apogranite, Central Eastern Desert, Egypt

Abstract: The northern part of Um Naggat granite massif (UNGM) has suffered extensive post-magmatic metasomatic reworking which results into the development of (Zr, Hf, Nb, Ta, U, Th, F)– and albite-enriched and greisenized apogranite body (UNAP) of 600 m thick, and more than 3 km in the strike length.
Albitization produced an enrichment in Zr (av. 2384 ppm), Hf (61), Nb (419), and U (43). The Th/U ratio ranges between 1. 33 and 1. 90. Extreme albitization (i. e. the albitite rock) is characterized by sharp decrease in the rare metals contents. However, extreme greisenization (i. e. endogreisen bodies) is characterized by a considerable enrichment in Zr (av. 5464 ppm), Hf (143), Nb (2329), Ta (152), U (66) and Th (178). The Th/U ratio ranges between 1. 57 and 3. 60. In contrast to extreme greisenization, it seems that extreme albitization does not apparently change the fluid pH and therefore poor amounts of rare metals are localized in the albitites.
It is suggested that the presence of Na⁺, H⁺ and F^- in the ore fluids was essential to stablize complexes of Zr, Hf, Nb, Ta, U, Th, and HREE during extraction and transportation. In contrast, contemporaneous decrease of temperature and increasing pH due to decreasing pressure are considered the essential factors for localization of disseminated mineralization of Zr and Nb in the apical parts of the UNAP. The enhanced uranium content in the alteration facies of UNAP coupled with the absence of significant uranium mineralization may indicate the metalliferous rather than mineralized nature for the UNAP. The high uranium contents are stabilized in refractory accessory minerals. However, with repect to Zr and Nb, the UNAP especially the albitized and greisen facies, can be categorized as a mineralized productive granite.     

Coprecipitation of Ti,Mo, Sn and Sb with fluorides and application to determination of B,Ti, Zr,Nb, Mo,Sn, Sb,Hf and Ta by ICP-MS

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.     

电感耦合等离子体质谱法测定岩石样品中的锆铌铪钽两种预处理方法的比较

研究了微波消解酸溶和过氧化钠碱熔两种测定岩石样品中锆、铌、铪、钽前处理方法,利用电感耦合等离子体质谱法进行测定。对所选用不同种类的岩石国家标准物质样品进行了条件实验,结果表明:采用过氧化钠碱熔法处理岩石样品后,锆、铌、铪、钽的测量值准确度高,且相对标准偏差(RSD,n=10)小于6%,该方法更适用于岩石样品中锆、铌、铪、钽的测定。     

延边开山屯花岗闪长岩-石英闪长岩体年代学、地球化学特征及对古太平洋板块俯冲作用时限的制约

近年来古太平洋构造域的构造演化备受学者关注。本文报道的延边开山屯地区花岗闪长岩-石英闪长岩体LAICP-MS U-Pb年龄表明其形成时间为早侏罗世早期(198±1Ma),所采样品可根据Zr/Hf值分为高Zr/Hf值组花岗闪长岩和低Zr/Hf值组石英闪长岩。高Zr/Hf值组花岗闪长岩起源深度浅,富集Rb、Th、U、K等大离子亲石元素(LILEs),贫Nb、Ta、Ti等高场强元素(HFSEs),具壳源岩浆的特点。低Zr/Hf值组为壳源岩浆与来自深部的亏损地幔岩浆混合而成,岩石亏损Nb、Ta、Zr、Hf、Ti等高场强元素,具有典型的弧型岩浆地球化学特征。岩体中存在细粒闪长质包体,镜下可见针柱状磷灰石。开山屯岩体属钙碱性系列岩石,结合前人资料,认为其与该地区同时代火成岩组成北-东向分布的早侏罗世活动大陆边缘型火成岩带,而位于该带西侧的小兴安岭-张广才岭地区存在同时代弧后拉张带,两者构成典型的大陆弧与弧后拉张带模型,共同揭示了早侏罗世早期古太平洋板块对东北地区的俯冲作用。     

超高压榴辉岩金红石中高场强元素变化的控制因素及其地球动力学意义

利用LA-ICP-MS对CCSD-MH超高压榴辉岩中金红石进行了详细的原位微区微量元素组成分析.金红石中高场强元素Nb和Ta含量主要受全岩Nb、Ta和TiO₂含量控制, Zr、Hf含量比较稳定基本不受全岩含量影响.粒间金红石中, 同一颗粒金红石核部Zr含量系统高于边部, 而边部则出现了明显的Pb和Sr富集特征.CCSD-MH榴辉岩中金红石与全岩的Nb/Ta比值呈现明显的不一致性.全岩Nb/Ta比值明显低于金红石且与全岩TiO₂含量负相关, 而金红石的Nb/Ta比值与全岩Nb、Ta含量和Nb/Ta比值没有明显的相关关系.金红石和全岩之间非完全耦合的Nb/Ta组成表明, 金红石并非形成于原岩的结晶过程中而是在超高压变质作用过程中形成, 尽管金红石是榴辉岩中Nb、Ta含量的主要载体矿物, 但金红石的Nb/Ta比值并不一定能完全代表全岩的特征, 而与全岩Nb、Ta和TiO₂的含量有关.粒间金红石核部Zr含量所记录的温度与粒径之间具有明显的正相关性, 反映金红石中的Zr在其形成后没有封闭.粒间金红石所表现出的明显的边部富集Pb和Sr的特征, 反映了后期流体活动对金红石组成的影响.这些研究结果为金红石中Zr在高温下的扩散作用和后期流体活动的影响提供了重要证据, 这可能是利用金红石Zr含量地质温度计计算的苏鲁-大别榴辉岩变质温度(598~827℃) 偏低的主要原因.      

Major and trace element variation in ilmenite in the Skaergaard Intrusion: petrologic implications

Ilmenite separates from the floor (LS), roof (UBS), and wall (MBS) sequences of the Skaergaard Intrusion were analyzed for major and trace elements using DCP-AES and ICP-MS techniques. In all three sequences, FeO progressively increases, and MgO and Al₂O₃ progressively decrease with differentiation. Although trace element abundances are, in general, higher in UBS ilmenite than in MBS and LS ilmenite, all three sequences have similar trends for trace element abundance vs. crystallization. Ba, Cs, Rb, Sr, Th, U, Y, and the REEs are excluded elements in ilmenite, and remained at low abundances during differentiation. Cr, Ni, Sc, and V are included elements in ilmenite and other mafic phases, and decreased during differentiation. V contents in ilmenite, however, do not decrease significantly until the upper part of the middle zone, suggesting that magnetite did not begin to affect the magma differentiation trend until much later than when it first appears in the intrusion. Hf, Nb, Ta, and Zr, which are strongly excluded elements in silicates, are included elements in ilmenite. The element ratios Zr/Hf, Y/Ho, Nb/Ta, and U/Th are relatively constant in Skaergaard ilmenite from different parts of the intrusion, suggesting that fluid transport did not significantly effect these elements during differentiation or post-solidification cooling. Calculated partition coefficients for ilmenite in the Skaergaard Intrusion are similar to those reported from previous studies of lunar and terrestrial basalts and kimberlites, and for most elements are significantly lower than those reported for ilmenite in rhyolitic magma. Similar D_i's for Zr, Hf, Nb, and Ta suggest that ilmenite crystallization did not significantly affect Zr/Nb or Hf/Ta in the Skaergaard magma, but the ratios of Zr, Hf, Nb, or Ta to other high field strength elements, such as Th, U, Y, or the REEs, may have been altered by ilmenite fractionation.     

Determination of Rare Earth Elements, Y, Th, Zr, Hf, Nb and Ta in Geological Reference Materials G-2, G-3, SCo-1 and WGB-1 by Sodium Peroxide Sintering and Inductively Coupled Plasma-Mass Spectrometry

Data are reported for rare earth elements (REE), Y, Th, Zr, Hf, Nb and Ta in four geological reference materials using sodium peroxide (Na₂O₂) sintering and inductively coupled plasma-mass spectrometry. The described procedure was used by students during their thesis work. A compilation of their reference material data acquired over one year of laboratory work demonstrates the ease and reliability of the method and the high reproducibility of the analytical results. Relative standard deviations of up to thirty six measurements of one reference material were lower than 5% for Y and the REE. Reproduciblities of Zr, Hf, Nb, Ta and Th were higher at between 5% and 10%, and can be attributed to the inhomogeneous distribution of zircon and other trace mineral phases and uncorrected drift effects. The concentration data are compared to reference and literature values and demonstrate that the procedure is also accurate. New data on G-3 show some systematic deviations from G-2, which are statistically significant.     

三江地区澜沧江带南段半坡杂岩体锆石U-Pb年龄、岩石地球化学特征及板块构造环境

半坡杂岩体位于滇西澜沧江构造岩浆带南段,岩体主要由橄榄岩、辉石岩、辉长岩和辉长闪长岩等镁铁 超镁铁质岩组成。通过ID-TIMS锆石U-Pb年代学方法对半坡杂岩体中辉长闪长岩进行精确定年,获得其结晶年龄为(294.9±2.6) Ma,表明半坡杂岩体的形成时代为早二叠世。半坡杂岩体中不同类型岩石微量元素、稀土元素和同位素组成相似,均呈现轻稀土元素(LREEs)相对于重稀土元素(HREEs)弱到中等富集,高场强元素Nb、Ta、Zr和Hf相对亏损的特征,εNd(t=295 Ma)为正值,在+3.4~+6.6,接近亏损地幔值,这些特征与典型的大洋岛弧玄武岩的特征相似。混合计算表明,半坡杂岩体母岩浆为地幔楔部分熔融,加上约2%~7%源于大洋俯冲沉积物的富硅熔浆和蚀变洋壳流体形成的岛弧玄武质岩浆。上述年龄和同位素数据提供了早二叠世早期南澜沧江地区洋内俯冲的可靠证据。     

青海泽库赛日迪印支期中基性岩体地球化学特征及构造背景

青海泽库东南赛日迪附近产出的印支期中基性岩体前人研究较少.对该岩体进行地球化学、构造背景及岩浆演化方面研究,结果表明,赛日迪岩体硅量中等、高镁铁、低铝、低钾钠,属准铝质钙碱性系列.富集Rb,K,Pb等大离子亲石元素(LILE)和Th,U,Ta,Nb,Hf等高场强元素(HFSE).普遍贫Ba,Sr等大离子亲石元素(LILE)和P,Zr,Ti等高场强元素(HFSE).稀土元素含量较低,轻稀土元素相对富集,轻稀土元素较重稀土元素分馏明显.Eu略显负异常,表现为同源岩浆成分特征.LREE与SiO2相关性不强,Nb/U、Nb/La远低于全球MORB、OIB值,Nb/Ta和Zr/Hf与原始地幔值相当,低Sm/Yb值,La/Nb和La/Ta指数指示赛日迪中基性岩可能为地幔源,岩浆经历部分熔融岩浆演化过程,上升过程中未受地壳物质混染.构造环境判别赛日迪中基性岩为钙碱性玄武岩,形成于板内环境,与板块碰撞作用有一定联系.     

Mineralogical and geochemical investigations of the Dajia Salento-type bauxite deposits,western Guangxi,China

The Dajia Salento-type bauxite deposit in western Guangxi is hosted within the Quaternary ferrallitic soil profile, and it formed via breaking up, weathering and oxidizing of Permian bauxite orebodies occurring as a semi-continuous layer in the upper Permian. Mineralogical analyses reveal that diaspore, hematite and kaolinite are the major minerals in bauxite ores with small amounts of anatase, chamosite, gibbsite, goethite, illite, zircon, quartz and pyrite. The ore texture and mineral assemblage reveal that the depositional/diagenetic environment of the Dajia bauxite was much close to phreatic environment. Both the ore texture and the morphology of zircon grains also indicate that most of the bauxitic soils were transported a short distance. Diaspore is suggested to be non-metamorphic in origin and mainly formed in a reducing condition of diagenetic environment, while kaolinite is the product of the in situ epigenetic replacement of alumina in diaspore by dissolved silica. Geochemical analyses indicate that Al₂O₃, Fe₂O₃, SiO₂ and TiO₂ are the main components of the bauxite ores and trace elements such as Zr, Hf, Nb, Ta, Th and U were enriched during the bauxitization process. Simultaneously, Zr vs. Hf and Nb vs. Ta show a high correlation. Geochemical indices such as Zr/Hf, Nb/Ta and Eu/Eu* (among others) denote that the magmatic rocks related to the Emeishan plume in western Guangxi and the carbonates in the underlying Maokou Formation provided the main sources of material for the bauxite ores.     

甘肃靖远上泥盆统沙流水组沉积地球化学特征及其物源分析

甘肃靖远上泥盆统沙流水组沉积地球化学研究表明:砂岩较泥质岩含有较高的SiO2含量和斜长石,而泥质岩较砂岩含有较高的铁镁质组分和含钾矿物.砂岩和泥质岩样品均亏损Nb、Ta、Sr元素.砂岩中部分样品富集Zr、Hf元素和强烈的Eu的负异常,部分样品显示Zr、Hf亏损和弱的负Eu异常.泥质岩样品均富集Nj、Cr元素,但具有较强...     

Geochemistry of highly-undersaturated ocean island basalt suites from the South Atlantic Ocean: Fernando de Noronha and Trindade islands

The volcanic rocks of the South Atlantic Ocean islands of Fernando de Noronha and Trindade comprise a diverse magmatic series ranging from nephelinites and basanites to phonolites and, on Fernando de Noronha, trachytes. All rock types are highly silica undersaturated with the exception of Fernando de Noronha trachytes_, and have high abundances of incompatible trace elements and strongly LREE (light rare earth element)-enriched REE patterns. Crystal fractionation of parental basanitic magmas produced evolved phonolites and trachytes which display severe trace-element fractionation, even among trace elements (Nb, Ta, Zr, Hf) which normally behave highly incompatibly during crystallisation of alkaline magmas. Moderately to highly evolved compositions develop strongly MREE (middle REE)-depleted REE patterns, and become increasingly depleted in elements such as Nb and, in particular, Ta. Ratios of Nb/Ta and Zr/Hf are highly fractionated in phonolites (60–65, 64–77 respectively in Fernando de Noronha phonolites) compared to ratios in basanites (14, 45 respectively). The compatibility of Nb, Ta, and the REE, and the strong fractionation of Nb/Ta and Zr/Hf ratios and the MREE, during crystallisation from basanite to phonolite are attributable to the crystallisation of small amounts (<5%) of sphene. Trace-element behaviour is relatively insensitive to the major phenocryst phases, and is controlled by minor phases in highly undersaturated alkaline suites. Incompatible trace-element ratios (e.g. La/Nb, Th/Ta) in nephelinites and basanites from Fernando de Noronha and Trindade are generally comparable with those in basaltic and hawaiitic OIB (ocean island basalt) lavas from other South Atlantic islands, but are distinct from those of Gough and Tristan da Cunha OIB. The mantle source for the highly undersaturated volcanism on Fernando de Noronha and Trindade is similar in trace-element characteristics to the typical OIB source which produces alkaline lavas with significant relative enrichment in Nb and Ta compared to other trace elements (as expressed by low La/Nb, Ba/Nb and Th/Ta ratios). The highly undersaturated nature of the magmas and the slight fractionation of some incompatible-element ratios (elevated Ba/Nb, Ba/Rb, Ba/Th etc.) is consistent with a smaller degree of melting of a typical OIB source, but with residual phlogopite in the source to account for significant K depletion and LIL-element fractionation.     

小兴安岭二龙山林场堆晶辉长岩地球化学特征及构造环境

小兴安岭北部二龙山林场辉长岩的主量、微量和稀土元素的测试分析结果显示: 二龙山辉长岩为钙碱性系列、偏铝质岩石; δEu 正异常,Sr 元素含量富集明显,具有堆晶辉长岩特征; Rb /Sr、Nb / Ta、LILE/HFSE、Th /Ta、Nb /U 和Nb /La 比值特征均显示,辉长岩岩浆来自受到俯冲流体交代的地幔源区。Nb /Zr、Th /Nb、Th /Ta 和Ta /Hf 比值特征及对Th /Hf --Ta /Hf 构造环境判别图解投点表明,二龙山辉长岩形成于陆内拉张环境。     

金沙江蛇绿岩带蛇纹岩中浅色岩类的成因

浅色岩类的岩石类型包括斜长岩和斜长花岗岩,它们均呈岩块状包裹于蛇纹岩中。浅色岩的正Ｅｕ异常明显,ＲＥＥ参数图解、Ｎｂ／Ｔａ和Ｚｒ／Ｈｆ值等均呈现分离结晶趋势,不相容元素Ｓｒ、Ｂａ、Ｎｂ、Ｔａ、Ｚｒ、Ｈｆ富集,相容元素Ｓｃ、Ｖ、Ｃｏ、Ｎｉ亏损,并与其寄主岩－蛇纹岩形成强烈的互补关系。这些特征表明,浅地是幔源超基性岩浆晚期结晶分异的产物。     

X射线荧光光谱法同时测定地质样品中铌钽锆铪铈镓钪铀等稀有元素

采用粉末压片法制样,选用标准样品,以经验α系数和散射线内标法校正基体效应和元素谱线重叠干扰,使用ZSXPrimusⅡX射线荧光光谱仪对一般地质样品中的铌、钽、锆、铪、铈、镓、钪、铀等稀有元素进行测定,分析结果与标准值和参考值吻合,12次测定的相对标准偏差(RSD)小于10%。     

Mechanisms of Archean crust formation inferred from high-precision HFSE systematics in TTGs

It has been proposed that Archean tonalitic-trondhjemitic-granodioritic magmas (TTGs) formed by melting of mafic crust at high pressures. The residual mineralogy of the TTGs (either (garnet)-amphibolite or rutile-bearing eclogite) is believed to control the trace element budget of TTGs. In particular, ratios of high-field-strength elements (HFSE) can help to discriminate between the different residual lithologies. In order to place constraints on the source mineralogy of TTGs, we performed high-precision HFSE measurements by isotope dilution (Nb, Ta, Zr, Hf) together with Lu-Hf and Sm-Nd measurements on representative, ca. 3.85-2.8 Ga TTGs and related rock types from southern West Greenland, W-India and from the Superior Province. These measurements are complemented by major and trace element data for the TTGs. Texturally homogeneous early Archean (3.85-3.60 Ga old) and Mesoarchean (ca. 3.1-2.8 Ga old) TTGs have both low Ni (<11 ppm) and Cr contents (<20 ppm), indicating that there was little or no interaction with mantle peridotite during ascent. Ratios of Nb/Ta in juvenile Eoarchean TTGs range from ca. 7 to ca. 24, and in juvenile Mesoarchean TTGs from ca. 14 to ca. 27. Even higher Nb/Ta (14-42) were obtained for migmatitic TTGs and intra-crustal differentiates, most likely mirroring further fractionation of Nb from Ta as a consequence of partial melting, fluid infiltration and migmatisation. In the juvenile TTGs, positive correlations between Nb/Ta and Gd/Yb, La/Yb, Sr/Y, Zr/Sm and Zr/Nb are observed. These compositional arrays are best explained by melting of typical Isua tholeiites in both, the rutile-bearing eclogite stability field (>15 kbar, high Nb/Ta) and the garnet-amphibolite stability field (10-15 kbar, low Nb/Ta). With respect to the low end of Nb/Ta found for TTGs, there is currently some uncertainty between the available experimental datasets for amphibole. Independent of these uncertainties, the TTG compositions found here still require the presence of both endmember residues. A successful geological model for the TTGs therefore has to account for the co-occurrence of both low- and high-Nb/Ta TTGs within the same geologic terrane. An additional feature observed in the Eoarchean samples from Greenland is a systematic co-variation between Nb/Ta and initial εHf(t), which is best explained by a model where TTG-melting occured at progressively increasing pressures in a pile of tectonically thickened mafic crust. The elevated Nb/Ta in migmatitic TTGs and intra-crustal differentiates can shed further light on the role of intra-crustal differentiation processes in the global Nb/Ta cycle. Lower crustal melting processes at granulite facies conditions may generate high-Nb/Ta domains in the middle crust, whereas mid-crustal melting at amphibolite facies conditions may account for the low Nb/Ta generally observed in upper crustal rocks.