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1.
《Chemical Geology》2003,193(1-2):109-125
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 Di'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. 相似文献
2.
《Chemie der Erde / Geochemistry》2019,79(2):384-398
Geochemical compositions of the Lower Cambrian Niutitang Formation shales in the southeastern Yangtze Platform margin were investigated for provenance, tectonic setting, and depositional environment. The shale samples are characterized by higher abundances of large ion lithophile elements (Cs, Ba, and Pb), lower abundances of high field strength elements (Cr, Sc, and Co) and transition elements (Th, Zr, Hf, Nb, and Ta) relative to average shale. North American shale composition (NASC) -normalized rare earth element (REE) patterns are observed, with negative Ce anomalies, negative Eu anomalies, and positive Y anomalies. The chemical index of alteration (CIA) varies from 68.67–74.93. Alkali and alkaline element contents and CIA values suggest that the source rocks have undergone moderate weathering. The index of compositional variability (ICV), Zr/Sc and Th/Sc ratios vary from 0.53 to 1.07, 5.31 to 8.18 and 0.52–1.02, respectively. ICV values and relationships between Zr/Sc and Th/Sc ratios indicate negligible sedimentary recycling. The Al2O3/TiO2 (14–26) and TiO2/Zr (56–77) ratios imply that the source rocks of the investigated shales had intermediate igneous compositions. However, Cr/V ratios and a La/Th–Hf discrimination diagram suggest that the intermediate compositional signal of the source rocks was derived from a mixture of 75% mafic and 25% felsic igneous rocks rather than intermediate igneous rocks. The major source was the Jiangnan continental island arc with bimodal igneous rocks, lying to the south of the study area, together with a contribution from granites and gneisses uplifted and eroded in the Yangtze Block. Discrimination of tectonic setting using major and trace elements indicates that the source rocks originated in a transitional setting from active continental to passive margin, consistent with the failed intracontinental rift model for the evolution of the South China plate. The Niutitang Formation shales were deposited in a rift basin setting under conditions of anoxic bottom water in a redox-stratified water column, with organic-rich shales prospective for shale-gas production being found in deep-water downslope and basin environments rather than the shallow-water shelf. 相似文献
3.
Sonja Aulbach Suzanne Y. O’Reilly Norman J. Pearson 《Contributions to Mineralogy and Petrology》2011,162(5):1047-1062
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. 相似文献
4.
V／Sc在CCSD主孔榴辉岩中的系统关系：一种可透视变质作用并指示基性岩浆作用的地球化学工具 总被引：1，自引：7，他引：1
和Fe一样，V和Sc都是过渡族金属元素，它们在地幔部分熔融和岩浆分异中的地球化学行为是近年来行星地质和岩石地球化学的研究热点之一。通过分析V和Sc在部分熔融和岩浆分异过程中的地球化学行为，发现V／Sc是可以透视岩浆成岩后所经历的变质、交代或流体作用的新的地球化学工具。本文通过系统分析中国大陆科学钻探工程主孔100～600米榴辉岩，尤其是540～600米钛铁矿一赤铁矿榴辉岩的V／Sc比值的变化特征，来进一步限定榴辉岩原岩可能的成岩过程。在CCSD主孔岩心中，和100～540m榴辉岩相比，540～600m段榴辉岩表现出以下十分特别的地球化学特征：（1）相当高的V，但十分低的Nb和Ta；（2）较高的TFeO，Fe2O3／FeO比值，高度变化且较高的Eu正异常（Eu／Eu^＋高达2.9）；（3）异常高的V／Sc比值（8．39～43．23，平均15．07），V／Sc比值和MgO之间呈负相关关系，但和Fe2O3／FeO之间呈正相关关系；（4）近乎正相同步变化的V和Fe2O3/、／FeO，但反相变化的V和Eu／Eu^＋。这些地球化学特征反映了原岩形成过程中，高度动态的斜长石分离结晶作用与岩浆氧逸度之间的负耦合关系，即在原始基性岩浆中，斜长石的分离结晶作用导致岩浆氧逸度升高，诱发钛磁铁矿和斜长石及单斜辉石的同步分离结晶作用，优先猎取大量的V和Fe，Sc主要分布在单斜辉石，导致所成堆晶的V和Fe含量升高及高度变化且增高的V／Sc比值，同时MgO，SiO2相对降低。这种过程导致上述的V和Fe2O3／FeO之间近乎同相变化关系．但反相变化的V和Eu／Eu^＋。CCSD主孔100～600m榴辉岩的V／Sc和MgO系统关系实际上透视了上述的过程，即除橄榄石堆晶作用外，含钛铁矿物相的分离结晶作用对形成的堆晶及相应岩浆的V、Sc和V／Sc比值的强烈控制作用。CCSD及区域地质所揭示的南北长约2000m，宽约500m的反S型、层序较完整的基性-超基性杂岩体所经历的岩浆过程有可能代表着大别-苏鲁超高压带中榴辉岩原岩经历了类似的过程。通过对较大规模榴辉岩及其伴生的超基性岩的V、Sc和V／Sc系统关系的系统研究可能进一步揭示更多类似的基性-超基性杂岩体，为厘定大别-苏鲁超高压带的碰撞前的物理和化学状态提供更好的限定。 相似文献
5.
中国大陆科学钻探主孔榴辉岩中石榴石和绿辉石原位激光探针分析及其成岩成矿指示意义 总被引：1，自引：0，他引：1
本文以中国大陆科学钻探主孔0～2000m岩芯中的榴辉岩为对象,运用EMPA和LA-ICP-MS技术,系统测定了榴辉岩中石榴石和绿辉石的主量与微量元素组成,并据此讨论了它们的成岩成矿意义.研究结果表明,CCSD主孔榴辉岩中石榴石富重稀土和Sc、Y、Co,而绿辉石则富中稀土和Pb、Sr、V,石榴石和绿辉石的高场强元素(特别是Nb、Ta)含量均很低.石榴石存在不同程度的Ce负异常,指示榴辉岩的形成过程中卷入有地表氧化条件下形成的风化沉积物.石榴石具有低的Zr/Y比值,绿辉石普遍具有高的Sr含量,这些特征说明榴辉岩(特别是高钛榴辉岩)的原岩可能为遭受过壳源物质混染与交代的富集地幔部分熔融的产物.高钛与低钛榴辉岩中石榴石和绿辉石在主量及微量元素组成上存在一定差别,总体而言,高钛榴辉岩中石榴石具高的MgO含量和较高的MgO/TFeO比值,以及较高的稀土和Sc含量,而绿辉石则相对富TFeO、MnO,并具有较高的Sr、Zr、Hf含量.高钛榴辉岩中石榴石和绿辉石常出现不同程度的Eu正异常,Cr含量均显著低于低钛榴辉岩.综合分析表明,高钛榴辉岩的原岩最可能为富斜长石的辉长质侵入岩,原岩组成的差异应是导致二类榴辉岩中石榴石和绿辉石矿物化学组成存在差异的主要原因. 相似文献
6.
For the first time occurrence of Ti rich Al depleted ultramafic cumulates having komatiitic signature in the northwestern fringe of Chotanagpur Gneissic Complex is presented. These rocks exhibit intrusive relationship with metasedimentary rocks and metaultramafites. Geochemically they are characterized by Mg# 79.1–91.60, high TiO2 (1.29–1.54 wt%), significantly low Al2O3/TiO2 and (Gd/Yb)n >1. Major oxides, trace and REE content suggest low degree of fractional crystallization and lesser degree of partial melting. These Al depleted komatiites are characterized by high concentration of incompatible elements than most suites of Barberton type komatiites. High Ti content suggests less degree of majorite garnet melting, leaving behind garnet in the restite. The rock shows higher Ti/Sc (190),Ti/V (22), Zr/Y (3), Zr/Sc (4), V/Sc (8), Zr/Sm (28) and Zr/Hf (47) ratios than primitive mantle and REE distribution pattern shows gentle slope from LREE to HREE in most samples pointing towards mantle metasomatism and crustal contamination during emplacement. The observed chemical characteristics indicate derivation of komatiite from an enriched mantle source and represent plume activity in an extensional tectonic regime of intracratonic setting. 相似文献
7.
Trace element compositions were determined (by instrumental neutron activation analysis; INAA) in 30 samples of synsedimentary volcanic ash-derived tonsteins and detrital claystones from coal seams within the late Permian coal-bearing formation of eastern Yunnan and western Guizhou Provinces, China. The characteristics of trace-element geochemistry in the tonsteins can be distinguished from those of detrital claystones because of the former's unique volcanic-ash origin. The detrital claystones are characterized by their relatively high content of V, Ti, Sc, Cr, Co and Ni, relatively low content of Th and U, Th/U ratio, and small negative Eu anomaly (Eu/Eu* 0.63–0.93). Overall, these trace element characteristics are consistent with a mafic source similar to the composition of basalt rocks in the erosional region on the western edge of the study area. In contrast, the tonsteins are low in V, Ti, Sc, Cr, Co and Ni contents and have a high Th/U ratio with a distinct negative Eu anomaly (Eu/Eu* normally in the range of 0.2–0.4), consistent with a silicic magmatic source.Within the group of tonsteins, those from the lower section (P2.1) of the coal-bearing formation are relatively high in Ti, Zr, Hf, Nb, Ta and rare earth elements (REE), as compared to those from the middle and upper sections (P2.2+3). In trace-element discrimination diagrams (scatter plots) of Hf–Ta, Ti–Ta, Ti–V, Hf–Sc, Lu–Hf and Lu–Th, tonsteins from the P2.1 horizon always fall in isolated distribution areas, separate from the tonsteins of the P2.2+3 horizon. These results suggest that the source materials of tonsteins from the two separate horizons were probably derived from volcanic ash falls of two distinctly different natures. Based on a comparison of the concentrations and assemblages of trace elements between various magmatic rocks, the source materials of tonsteins from P2.1 horizon were mostly composed of calc-alkalic, silica-poor volcanic ash (similar to rhyodacitic magma), whereas those from P2.2+3 were apparently more siliceous and K-rich (rhyolitic magma). Thus, tonsteins from the two different horizons are characterized by unique geochemical properties, which remain constant over a wide lateral extent. Integration of trace-elemental compositions with mineralogical and textural observations makes possible the establishment of tonstein stratigraphy, thus, facilitating more precise and reliable coal-seam correlations. 相似文献
8.
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 总被引：12，自引：8，他引：4
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。 相似文献
9.
东南沿海分布大面积的白垩纪晚期侵入岩。这些岩石可分为两期:其中115~100Ma以钙碱性系列岩石为主,岩石组合为辉长岩-闪长岩-花岗闪长岩-二长花岗岩-碱性长石花岗岩;而100~86Ma的岩石为碱性系列,岩石组合为石英二长斑岩-正长斑岩-碱性长石花岗岩。115~100Ma的辉长岩以角闪辉长岩为主,具有极高的CaO、MgO和Al_(2)O_(3)含量,具有极低的SiO_(2)(42.9%~53.8%)、全碱(K_(2)O+Na_(2)O:0.86%~5.28%)、Ba、Nb、Th、Rb和Zr含量,也具有极低的FeO^(T)/MgO、La/Yb和Zr/Hf比值,较高的Eu/Eu^(*)、Sr/Y比值和Sr含量,为基性-超基性堆晶岩。与辉长岩同期的闪长岩和细粒暗色包体具有较高的SiO_(2)(50.34%~63.68%),较低的CaO、P_(2)O_(5)、MgO、Al_(2)O_(3)含量,相对低的Eu/Eu^(*)和Sr/Y比值,变化较大的La/Yb和Zr/Hf比值,代表了从基性岩浆储库中抽取的富硅熔体。115~100Ma的花岗闪长岩和二长花岗岩类岩石为准铝质岩石,SiO_(2)含量变化较大(61.7%~75.3%),具有较低的FeO^(T)/MgO、Ga/Al比值和Nb、Zr及Nb+Zr+Ce+Y元素含量,显示出典型I型花岗岩的特征。这些花岗岩具有相对高的La/Yb、Eu/Eu^(*)和Zr/Hf比值和高的Sr、Ba和Zr含量。结合岩相学特征,这些花岗岩为堆晶花岗岩。而115~100Ma的碱性长石花岗岩具有极高的SiO_(2)含量(大于75%),低的Eu/Eu^(*)、La/Yb、Zr/Hf和Sr/Y比值,具有低的Ba、Sr和Zr含量和高的Rb、Nb、Y和Th含量和Rb/Sr比值,表明这些花岗岩是由富硅岩浆储库中抽离的高硅熔体侵入地壳形成。100~86Ma期间形成的二长斑岩和正长斑岩具有极高的全碱含量,可以达到8%~12%,其SiO_(2)主要集中在60%~70%,具有极高的Zr、Sr和Ba含量和Eu/Eu^(*)、La/Yb和Sr/Y比值,显示出堆晶花岗岩的特征。而100~86Ma期间形成的大部分碱性长石花岗岩具有极高的SiO_(2)含量(大于75%),并显示出A型花岗岩的特征,具有高的Rb/Sr比值和高的Rb、Y和Th和低的Ba、Sr含量和低的Zr/Hf、La/Yb、Eu/Eu^(*)和Sr/Y比值,表明它们是由富硅岩浆储库抽离的高硅熔体侵入浅部地壳形成。东南沿海高硅花岗岩的形成和穿地壳岩浆系统密切相关,高硅花岗岩是由浅部地壳内晶体-熔体分异产生的熔体侵入地壳所形成,而高硅花岗岩的地球化学特征与岩浆储库的水及挥发份含量密切相关。115~100Ma期间,从富水的岩浆储库抽离的熔体形成具有低高场强元素含量和低Rb/Sr比值的高硅花岗岩,这一过程与古太平洋板块俯冲有关;100~86Ma期间,从富挥发份的岩浆储库抽离的熔体形成碱性特征、富含高场强元素和具有高的Rb/Sr比值的高硅花岗岩,这一过程和古太平洋板块回撤软流圈上涌有关。 相似文献
10.
金沙江蛇绿岩带蛇纹岩中浅色岩类的成因 总被引：4，自引：0，他引：4
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。 相似文献
11.
Cigdem Saydam Eker Ferkan Sipahi Abdullah Kaygusuz 《Chemie der Erde / Geochemistry》2012,72(2):167-177
Trace elements and rare earth elements (REEs) of Lias-aged cherts in the Gumushane area were studied in order to understand their origin and depositional environment. Twenty three chert samples from five stratigraphic sections were analysed by inductively coupled plasma-mass spectrometry, X-ray diffraction, and mineralogical investigation. Lias cherts in the study area are microcrystalline, cryptocrystalline quartz, and megaquartz depending on mineralogical content. Trace elements of the cherts were compared with PAAS, Co, Y, and Th had stronger depletions in the five sections, whereas V, Ni, Zr, Nb, and Hf had smaller depletions. The distribution of Zr, Hf, and Ta yields Zr/Hf, Zr/Ta and Hf/Ta ratios (25/645, 37/665, and 0.18/3, respectively) that differ from those of chondrites and average upper continental crust, suggesting that these elements are likely non-detrital but are sourced from seawater. Th/U ratios range from 0.04 to 0.45 and are lower than those of the upper continental crust (average: 3.9). Lias-aged cherts have low total REE abundances and stronger depletions in five sections of the PAAS and chondrite-normalised plots. The cherts are characterised by a positive Eu anomaly (average: 4.9) and LREE-enrichment (LaN/YbN = average: 3.5). In addition, about one-half of the cherts exhibit positive Ce anomaly (range: 0.25–2.58), chondritic Y/Ho values (range: 3.3–60), and low (La/Ce)N values (average: 1.8). REE and trace element abundance in Lias cherts indicate that these elements were likely derived from hydrothermal solutions, terrigenous sources, and seawater. The REE patterns of the cherts show that they were probably deposited close to a continental margin. 相似文献
12.
Five Devonian plutons (West Charleston, Echo Pond, Nulhegan, Derby, and Willoughby) that constitute the Northeast Kingdom batholith in Vermont show wide ranges in elemental abundances and ratios consistent with major crustal contributions during their evolution. The batholith consists of metaluminous quartz gabbro, diorite and quartz monzodiorite, peraluminous granodiorite and granite, and strongly peraluminous leucogranite. Contents of major elements vary systematically with increasingSiO<2 (48 to 77 wt.%). The batholith has calc-alkaline features, for example a Peacock index of 57, and values for K<2O/Na2O (<1), K/Rb (60–350), Zr/Hf (30–50), Nb/Ta (2–22), Hf/Ta (up to 10), and Rb/Zr (<2) in the range of plutonic rocks found in continental magmatic ares. Wide diversity and high values of minor- and trace-element ratios, including Th/Ta (0.5–22), Th/Yb (0–27), Ba/La (0–80), etc., are attributed to intracrustal contributions. Chondrite-normalized REE patterns of metaluminous and relatively mafic intrusives have slightly negative slopes (La/Ybcn<10) and negative Eu anomalies are small orabsent. The metaluminous to peraluminous inter-mediate plutons are relatively enriched in the light REE (La/Ybcn>40) and have small negative Eu anomalies. The strongly peraluminous Willoughby leucogranite has unique trace-element abundances and ratios relative to the rest of the batholith, including low contents of Hf, Zr, Sr, and Ba, low values of K/Rb (80–164), Th/Ta (<9), Rb/Cs (7–40), K/Cs (0.1–0.5), Ce/Pb (0.5–4), high values of Rb/Sr (1–18) low to moderate REE contents and light-REE enriched patterns (with small negative Eu anomalies). Flat REE patterns (with large negative Eu anomalies) are found in a small, hydrothermally-altered area characterized by high abundances of Sn (up to 26 ppm), Rb (up to 670 ppm), Li (up to 310 ppm), Ta (up to 13.1 ppm), and U (up to 10 ppm). There is no single mixing trend, fractional crystallization assemblage, or assimilationscheme that accounts for all trace elementvariations from quartz gabbro to granite in the Northeast Kingdom batholith. The plutons originated by mixing mantle-derived components and crustal melts generated at different levels in the heterogeneous lithosphere in a continental collisional environment. Hybrid rocks in the batholith evolved by fractional crystallization and assimilation of country rocks (<50% by mass), and some of the leucogranitic rocks were subsequently disturbed by a mild hydrothermal event that resulted in the deposition of small amounts of sulfide minerals. 相似文献
13.
Statistical data on major, trace and rare-earth elements in wolframite from the quartz vein-and greisen-type tin deposits
in the Dupangling orefield reveal: (1) The components in wolframite can be divided into two relatively independent groups:
the WO3-Nb-Ta-Sc-REE group, in which WO3 is negatively correlated with the others and the FeO-MnO-Sn group, in which MnO is negatively correlated with the other two;
(2) In general, REE fractionation is not significant, reflected mainly by the separation of Eu from other REE’s. LREE and
HREE increase or decrease simultaneously, with HREE being more variable; (3) Nb, Ta, Sc, REE substitute for W, and Sn may
enter into wolframite lattice accompanied by Fe-Mn substitution; (4) In contrast to wolframite in quartz veins, which is poor
in REE, Nb, Ta and Sc and has highδ Eu values and LREE / HREE and Nb/Ta ratios, wolframite in greisen is rich in REE, Nb, Ta, Sc and has lowδ Eu values and LREE/HREE and Nb/Ta ratios; and (5) The contents and ratios of trace elements and REE partitioning parameters
of wolframite can be used as guide for prospecting. 相似文献
14.
Combined Sm–Nd and Lu–Hf age and isotope data indicate that Mg- and Cr-rich ultramafic rocks at Sandvik, Western Gneiss Region
(WGR), Norway, originated from depleted Archean lithospheric mantle that was chemically and physically modified in Middle
Proterozoic time. The Sandvik outcrop consists of garnet peridotite and garnet-olivine pyroxenite and thin garnet pyroxenite
layers. These contain two principal mineral assemblages: an earlier porphyroclastic assemblage of grt + opx + cpx ± ol (1,200–1,000°C,
40–50 kbar) and a later kelyphitic assemblage of grt + spl + am ± opx ± ol (700–750°C; 12–18 kbar). A CHUR Hf model age indicates
a period of melt extraction at ca. 3.3 Ga for garnet peridotite, reflecting extremely high Lu/Hf ratios and very radiogenic
present-day 176Hf/177Hf (εHf=+2,165). Lu–Hf garnet-cpx-whole rock ages of two olivine-bearing samples (garnet peridotite and garnet-olivine pyroxenite)
from the outcrop are ca. 1,255 Ma, whereas two olivine-free garnet pyroxenites yield Lu–Hf ages of ca. 1,185 Ma. All Sm–Nd
garnet-cpx-whole rock ages of these samples are significantly younger (ca. 1,150 Ma for garnet peridotite and ca. 1,120 Ma
for garnet pyroxenite). The isotope systematics indicate that the Lu–Hf ages represent cooling from an earlier period of formation/recrystallization
for garnet peridotite whereas they probably reflect formation/recrystallization ages of the garnet pyroxenite. The Sm–Nd ages
and isotope systematics of the garnet peridotite samples are consistent with an episode of LREE metasomatism, perhaps facilitated
by a fluid of carbonatitic composition that strongly decoupled Sm–Nd and Lu–Hf. The Sm–Nd ages of the garnet pyroxenite may
represent either LREE metasomatism or cooling, and, like the peridotites, Lu–Hf ages are older than Sm–Nd ages. The age data,
as well as the inferred Nd isotope composition of the fluid that affected the olivine-bearing samples, suggest that these
rocks were not in contact during the LREE metasomatic event. Moreover, the pyroxenite layers cannot have been emplaced as
magmas into the host peridotite. The pyroxenite layers are interpreted to be tectonically juxtaposed with the host olivine-bearing
samples sometime after 1,150 Ma but before development of kelyphite. 相似文献
15.
Komatiites of the Karasjok Greenstone Belt, northern Norway, show two unusual features: they have certain compositional differences compared with other komatiites, and they are largely volcaniclastic in origin. Their geological setting suggests that the komatiites were crupted into shallow water, thus permitting phreatomagmatic eruption, in a small ocean basin that opened in the Baltic Shield. The major oxides (except for TiO2), the trace elements Y, Sc, V, heavy rare earth elements (HREE), Cr, Co, Ni and the platinum group elements (PGE) cover similar ranges to those observed in other komatiites, but TiO2, Sm, Zr and Hf (Ti-associated elements, TAE) are enriched compared with abundances commonly reported for komatiites. Thus, the Karasjok komatiites have interelement ratios 2 to 3 times greater than chondritic between the TAE and the HREE, PGE, Sc, V, Y, Al (HRE-associated elements, HAE). The light rare earth elements (LREE), Ta and Th are enriched in some samples relative to Ti, Sm, Zr, and Hf, but are depleted in others. One group of rocks that is similar to the Karasjok komatiites both in terms of geological setting and geochemistry is the Baffin Bay picrites. The reason for the high concentrations of TAE in the Karasjok komatiites could be that they formed at lower degrees of partial melting than most komatiites. The greater-than-chondritic TAE/HAE ratios indicate that garnet was a residual phase during their formation, requiring that the melt formed at a pressure greater than 40 kb. A model involving decompression melting of a mantle plume rising in a rifting environment, can explain the main features of the Karasjok komatiites. 相似文献
16.
Xuefei Liu Qingfei Wang Jun Deng Qizuan Zhang Silei Sun Jianyin Meng 《Journal of Geochemical Exploration》2010
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. 相似文献
17.
青海鄂拉山地区陆相火山岩地球化学特征及构造环境 总被引：2，自引：0，他引：2
鄂拉山岩浆岩带晚三叠世火山岩为中-中酸性火山岩组合,由玄武安山岩、安山岩、英安岩、流纹岩及少量火山碎屑岩等组成,岩石蚀变强烈,成层性差,柱状节理发育,具典型的陆相喷发特点.火山岩属铝饱和类型,里特曼指数(δ)及岩石学等显示具钙碱性特征, (FeO/MgO)、K2 O/Na2O显示可能具有陆缘岛弧环境的特性;轻稀土元素分馏程度高且富集,δEu小于1,为弱负异常,稀土元素配分模式曲线与岛弧型稀土元素配分模式图相似;微量元素Rb、Ba、Th等元素明显富集,而Ti、Y、Yb、Sc、Cr等元素较亏损.Nb/Zr、La/Nb、Th/Ta、Th×Ta/Hf2等特征反映鄂拉山组火山岩产于陆缘火山弧环境.结合区域地质背景、岩石地球化学及构造环境等特征,认为鄂拉山地区晚三叠世火山岩产于大陆碰撞与陆缘弧并存的环境. 相似文献
18.
HFSE systematics of rutile-bearing eclogites: New insights into subduction zone processes and implications for the earth’s HFSE budget 总被引：1，自引：0，他引：1
The depleted mantle and the continental crust are generally thought to balance the budget of refractory and lithophile elements of the Bulk Silicate Earth (BSE), resulting in complementary trace element patterns. However, the two high field strength elements (HFSE) niobium and tantalum appear to contradict this mass balance. All reservoirs of the silicate Earth exhibit subchondritic Nb/Ta ratios, possibly as a result of Nb depletion.In this study a series of nineteen orogenic MORB-type eclogites from different localities was analyzed to determine their HFSE concentrations and to contribute to the question of whether subducted oceanic crust could form a hidden reservoir to account for the mass imbalance of Nb/Ta between BSE and the chondritic reservoir. Concentrations of HFSE were analyzed with isotope dilution (ID) techniques. Additionally, LA-ICPMS analyses of clinopyroxene, garnet and rutile have been performed. Rutile is by far the major host for Nb and Ta in all analyzed eclogites. However, many rutiles revealed zoning in Nb/Ta ratios, with cores being higher than rims. Accordingly, in situ analyses of rutiles have to be evaluated carefully and rutile cores do not necessarily reflect a bulk rock Nb and Ta composition, although over 90% of these elements reside in rutile.The HFSE concentration data in bulk rocks show that the orogenic eclogites have subchondritic Nb/Ta ratios and near chondritic Zr/Hf ratios. The investigated eclogites show neither enrichment of Nb compared to similarly incompatible elements (e.g. La), nor fractionation of Nb/Ta ratios relative to MOR-basalts, the likely precursor of these rocks. This indicates that during the conversion of the oceanic crust to eclogites in most cases, (1) HFSE and REE have similar mobility on average, possibly because both element groups remain in the down going slab, and (2) no significant fractionation of Nb/Ta occurs in subducted oceanic crust. With an average Nb/Ta ratio of 14.2 ± 1.4 (2s.e.), the investigated eclogites cannot balance the differences between BSE and chondrite. Additionally, as their average Nb/Ta is indistinguishable from the Nb/Ta of MORB, they are also an unlikely candidate to balance the potentially small differences in Nb/Ta between the continental crust and the mantle. 相似文献
19.
20.
白云岩风化剖面元素地球化学特征:对黔中九架炉组“三稀金属”富集机制的启示 总被引：2，自引：1，他引：1
黔中早石炭世九架炉组铝土矿含矿岩系富集Ti、Li、Sc、V、Ga、Nb、Ta、Zr、Hf、Th和稀土(REEs)等"三稀金属",具有成为独立矿床或伴生资源的潜力。这些元素大部分与九架炉组共有同一母岩,且富集程度受母岩的成分和风化作用控制。本研究选取九架炉组母岩乌当娄山关群白云岩和纳雍牛蹄塘组泥质白云岩的现代风化剖面为研究对象,研究元素在风化作用过程中的迁移特征及分布规律,进而为九架炉组微量元素的富集机制提供启示。研究获得以下认识:1)依据剖面结构、ZrHf、Nb-Ta、Y-Ho二元图特征及REE配分曲线和Eu/Eu*值的相似性表明研究区土层主要来源于基底或母岩的风化; 2)白云岩风化成土过程中Si、Fe、Cr、As、Sb、Ti、Nb、Ta、Zr、Hf、Th、REEs等元素化学性质相对稳定,富集程度较高,而Ca、Mg、Na、K、Sr、P、Mo、Cd等元素化学性质活泼,容易淋失亏损; 3)纳雍剖面REEs~(3+)和Ca~(2+)半径差与REEs富集系数相关性良好,表明碳酸盐岩风化过程中,含钙矿物磷灰石是稀土元素分配的重要控制因素; 4)九架炉组的母岩也是Ti、Li、Sc、V、Ga、Nb、Ta、Zr、Hf、Th等微量元素的主要物质来源,母岩风化过程中,这些微量元素首先在副矿物、黏土矿物、铝矿物及磷灰石等矿物相中初步富集,之后随风化碎屑物一起沉积形成微量元素超常富集地层; 5)纳雍剖面地表和地下水提供了部分P、Be、Zn、Sb、Pb、Y及REEs来源,指示水体迁入作用也是九架炉组REEs富集的重要原因。研究表明黔中九架炉组微量元素的来源较复杂,风化-沉积过程中,化学性质稳定的元素残留在风化碎屑物中并被搬运-沉积在负地形中,而化学性质活泼的元素首先被带入水体,在沉积-成岩过程中特定条件下发生二次富集作用(例如次生矿物的形成及吸附)形成微量元素富集的地层。 相似文献