山西省石墙区铝土矿地质与地球化学特征研究

[摘 要]山西省原平市石墙区铝土矿属于典型的喀斯特型铝土矿。含矿岩系自下而上包括铁质粘土层、铝土矿层、粘土层,且含矿岩系一般包含两个明显的沉积旋回。矿体主体呈层状、似层状产出,矿石结构以隐晶质结构为主,局部出现碎屑和豆鲕粒结构。矿石构造大都为块状构造。矿物学分析显示,硬水铝石、针铁矿、锐钛矿、高岭石是主要的组成矿物,另外还含有石英、伊利石、绿泥石等矿物。地球化学分析显示,主量元素主要包括Al₂O₃、SiO₂、Fe₂O₃、H₂O⁺及TiO₂,微量元素中碱性和碱土元素Li、Sr、Be、Cs、Ba 及酸土元素Zr、Hf、Nb、Ta、W 均表现为明显富集,且Zr 和Hf 之间以及Nb 和Ta 之间具有高度的相关性。地球化学指标Zr/ Hf、Nb/ Ta 以及Eu/ Eu^*- TiO₂/ Al₂O₃图解显示,底板碳酸盐岩是山西省原平市石墙区铝土矿的重要源岩。     

NEW TRACE ELEMENT AND REE DATA IN THIRTEEN GSF REFERENCE SAMPLES BY ICP-MS

Analytical data on 34 geochemically significant trace elements (Sc, V, Cr, Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, Hf, Ta, Pb, The, U and REE) by using Inductively Coupled Plasma Mass Spectrometry (ICP-MS), for 13 reference rock samples obtained from the Geological Survey of Finland are presented. For many elements, especially most of the heavy-REE, concentrations are reported here for the first time.     

Partitioning of trace elements between rutile and silicate melts: Implications for subduction zones

Mineral/melt trace element partition coefficients were determined for rutile (TiO₂) for a large number of trace elements (Zr, Hf, Nb, Ta, V, Co, Cu, Zn, Sr, REE, Cr, Sb, W, U, Th). Whilst the high field strength elements (Zr, Hf, Nb, Ta) are compatible in rutile, other studied trace elements are incompatible (Sr, Th, REE). In all experiments we found D_Ta > D_Nb, D_Hf > D_Zr and D_U > D_Th. Partition coefficients for some polyvalent elements (Sb, W, and Co) were sensitive to oxygen fugacity. Melt composition exerts a strong influence on HFSE partition coefficients. With increasing polymerization of the melt, rutile/melt partition coefficients for the high field strength elements Zr, Hf, Nb and Ta increase about an order of magnitude. However, D_Nb/D_Ta and D_Hf/D_Zr are not significantly affected by melt composition. Because D_U ? D_Th, partial melting of rutile-bearing eclogite in subducted lithosphere may cause excesses of ²³⁰Th over ²³⁸U in some island arc lavas, whereas dehydration of subducted lithosphere may cause excesses of ²³⁸U over ²³⁰Th. From our partitioning results we infer partition coefficients for protactinium (Pa) which we predict to be much lower than previously anticipated. Contrary to previous studies, our data imply that rutile should not significantly influence observed ²³¹Pa-²³⁵U disequilibria in certain volcanic rocks.     

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.     

Pedo-geochemical baseline content levels and soil quality reference values of trace elements in soils from the Mediterranean (Castilla La Mancha, Spain)

To evaluate trace element soil contamination, geochemical baseline contents and reference values need to be established. Pedo-geochemical baseline levels of trace elements in 72 soil samples of 24 soil profiles from the Mediterranean, Castilla La Mancha, are assessed and soil quality reference values are calculated. Reference value contents (in mg kg^?1) were: Sc 50.8; V 123.2; Cr 113.4; Co 20.8; Ni 42.6; Cu 27.0; Zn 86.5; Ga 26.7; Ge 1.3; As 16.7; Se 1.4; Br 20.1; Rb 234.7; Sr 1868.4; Y 38.3; Zr 413.1; Nb 18.7; Mo 2.0; Ag 7.8; Cd 4.4; Sn 8.7; Sb 5.7; I 25.4; Cs 14.2; Ba 1049.3; La 348.4; Ce 97.9; Nd 40.1; Sm 10.7; Yb 4.2; Hf 10.0; Ta 4.0; W 5.5; Tl 2.3; Pb 44.2; Bi 2.2; Th 21.6; U 10.3. The contents obtained for some elements are below or close to the detection limit: Co, Ge, Se, Mo, Ag, Cd, Sb, Yb, Hf, Ta, W, Tl and Bi. The element content ranges (the maximum value minus the minimum value) are: Sc 55.0, V 196.0, Cr 346.0, Co 64.4, Ni 188.7, Cu 49.5, Zn 102.3, Ga 28.7, Ge 1.5, As 26.4, Se 0.9, Br 33.0 Rb 432.7, Sr 3372.6, Y 39.8, Zr 523.2, Nb 59.7, Mo 3.9, Ag 10.1, Cd 1.8, Sn 75.2, Sb 9.9, I 68.0, Cs 17.6, Ba 1394.9, La 51.3, Ce 93.5, Nd 52.5, Sm 11.2, Yb 4.2, Hf 11.3, Ta 6.3, W 5.2, Tl 2.1, Pb 96.4, Bi 3.0, Th 24.4, U 16.4 (in mg kg^?1). The spatial distribution of the elements was affected mainly by the nature of the bedrock and by pedological processes. The upper limit of expected background variation for each trace element in the soil is documented, as is its range as a criterion for evaluating which sites may require decontamination.     

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。     

Trace Elements and Sr,Nd Isotope Geochemistry of the Lajimiao Norite-Gabbro from the North Qinling Belt1

Abstract The Lajimiao norite-gabbro complex, as a part of the ophiolites on the southern side of the North Qinling belt, consists of gabbro and norite-gabbro. They were derived from different magma series: the gabbro was derived from tholeiitic magma series with higher TiO₂, REE abundance and Fe³⁺ / Fe²⁺ ratio; norite-gabbro was derived from calc-alkali magma series with lower TiO₂, Fe³⁺ / Fe²⁺ ratio and REE abundance and much lower HREE abundance, which suggests that the source of the norite-gabbro magma was deeper and controlled by eclogite facies. Geochemical characteristics of both plutonic rocks are similar to those of island-arc basalts, such as relatively high contents of Ba, Pb and Sr and relatively low contents of Nb, Zr and Ni. The Sr, Nd isotopic characteristics of the Lajimiao norite-gabbro complex are similar to those of ophiolites. Its 8_Nd values are constant, about +2; whereas 8_Sr values have wide variation from — 6.4 to +31.2 and positively correlate with Na₂O, H₂O⁺ and CO₂ contents and the Fe³⁺ / Fe²⁺ ratio. The ?_Nd—Nd / Th, ?_Nd—La/Nb and ?_Nd—Ba/Nb diagrams clearly show that there were significant components of terrigenous sediments in the mantle source of the Lajimiao norite-gabbro complex. It suggests that large amount of sediments had been carried into the mantle by the subducted ancient Qinling sea plate during the Palaeozoic.     

塔里木盆地东南缘安南坝地区镁铁质麻粒岩的成因——来自地球化学及Sr-Nd-Pb同位素的制约

甘肃阿克塞县安南坝地区镁铁质麻粒岩呈脉状、透镜状赋存于新太古代米兰岩群和TTG片麻岩中。岩石主要由斜长石(Pl)+斜方辉石(Opx)+单斜辉石(Cpx)+角闪石(Amp)+磁铁矿(Mt)等组成。安南坝镁铁质麻粒岩中Ti、P、Nb、Ta、Th、Hf、Sr及REE等元素与Zr相关性较好,表明其在变质作用过程中保持基本稳定。地球化学数据显示其原岩属于拉斑玄武质岩系列,Si O_2、Ti O_2、Al_2O_3、P_2O_5含量相对较低,Ca O、Mg O含量相对较高。Mg~#值为41.52~43.09,低于原生玄武质岩石的Mg~#值,Fe_2O_3~T、Mg O、Ca O与Si O_2含量呈负相关性,指示原岩岩浆演化过程中可能发生了辉石、角闪石等镁铁质矿物的分异结晶作用。镁铁质麻粒岩∑REE较低,稀土元素配分模式为轻稀土元素弱富集、重稀土元素相对平坦的右倾型,Eu异常不明显(Eu/Eu~*=0.91~1.01)。岩石富集Rb、Ba、Sr等大离子亲石元素,亏损Nb、Ta、Zr、Ti等高场强元素,具有显生宙典型岛弧玄武质岩石的地球化学特征。Sr、Nd、Pb同位素组成显示镁铁质麻粒岩原岩源自富集地幔,并受到一定程度的地壳物质混染。构造环境分析表明安南坝镁铁质麻粒岩原岩形成于与俯冲有关的岛弧环境。在俯冲作用机制下,俯冲板片流体交代使地幔楔发生富集,形成富集地幔,随着(弧后)伸展作用的加强,进一步诱发富集地幔的部分熔融形成镁铁质岩浆,最终岩浆就位形成辉长岩或辉绿岩脉,后期在麻粒岩相变质作用条件下变质为镁铁质麻粒岩。     

挥发份对高硅岩浆演化趋势的制约:以东南沿海白垩纪晚期花岗岩类岩石为例SCIEI北大核心CSCD

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。     

Origin and evolution of topaz-bearing granites from the Nanling Range, South China: a geochemical and Sr–Nd–Hf isotopic study

Summary The F-rich Hongshan pluton in the eastern Nanling Range, southern China, is a topaz-bearing albite leucogranite. It is distinctive from other topaz-bearing felsic rocks in South China with respect to age, size, geochemical evolution and topaz mode and morphology. The Hongshan granites are highly peraluminous and characterized by high K₂O/Na₂O, Si, Rb, Cs, Nb, Ta and F, and low Ca, Ba, Sr, Zr, Hf, P, K/Rb, Zr/Hf and Eu/Eu^*. The granites show significant trace-element variations with magma evolution, with increasing Rb, Cs, Nb, Ta, Sn, W and decreasing Sr, Ba, Zr, Hf, Y, REE, Pb, Th, K/Rb, Zr/Hf, Th/U and Eu/Eu^*. These changes dominantly reflect fractional crystallization of plagioclase, biotite and accessory minerals such as zircon and monazite. The granites also exhibit a decrease in ɛNd(t = 225 Ma) from −7.9 to −11.7 with magma evolution. Modeling shows that the Nd isotopic variation could result from assimilation of the Taoxi Group wall rocks during fractional crystallization. The Hongshan pluton also shows spatial geochemical variations; the most evolved parts are located in the southeastern part of the pluton, which would be the most likely target area for rare-metal mineralization commonly associated with other topaz-bearing granites. Zircon grains from two rock types in the Hongshan body were analyzed in situ for U–Pb ages and Hf isotopic values. The concordant zircon grains mostly range from 218 to 230 Ma with an average of 224.6 ± 2.3 Ma (Indosinian). Some zircons with different internal structures and Hf isotope compositions, as well as monazite fragments, yield U–Pb ages of ca. 280 to 240 Ma, suggesting older thermal events in the studied area. The ɛHf(t) of these older zircons is strongly negative (−12.3), implying a crustal source with a Paleoproterozoic model age, similar to that for the Proterozoic Zhoutan Group. The main (∼225 Ma) zircon population exhibits less negative ɛHf(t) (−3.0 to −7.6) and Mesoproterozoic model ages, suggesting that the original magma of the Hongshan granite was generated from deeper Mesoproterozoic crust.     

Concentration and distribution of elements in Late Permian coals from western Guizhou Province,China

With the aim of better understanding geochemistry of coal, 71 Late Permian whole-seam coal channel samples from western Guizhou Province, Southwest China were studied and 57 elements in them were determined. The contents of Al, Ca, Co, Cr, Cu, Fe, Ga, Hf, K, Li, Mn, Mo, Nb, Ni, Sn, Ta, Ti, Th, U, V, Zr, and REEs in the Late Permian coals from western Guizhou Province are higher than the arithmetic means for the corresponding elements in the US coals, whereas As, Ba, Br, F, Hg, P, Se, and Tl are lower. Compared to common Chinese coals, the contents of Co, Cr, Cu, Ga, Hf, Li, Mn, Mo, Ni, Sc, Sn, Ti, U, V, Zn, and Zr in western Guizhou coals are higher, and As, F, Hg, Rb, Sb, Tl, and W are lower. Five groups of elements may be classified according to their mode of occurrence in coal: The first two, Group A, Tm–Yb–Lu–Y–Er–Ho–Dy–Tb–Ce–La–Nd–Pr–Gd–Sm, and Group B, As–Sr–K–Rb–Ba–F–Ash–Si–Sn–Ga–Hf–Al–Ta–Zr–Be–Th–Na, have high positive correlation coefficients with ash yield and they show mainly inorganic affinity. Some elements from Group B, such as Ba, Be, Ga, Hf, and Th, are also characterized by significant aluminosilicate affinity. In addition, arsenic also exhibits high sulfide affinity (r_S–Fe>0.5). The elements, which have negative or lower positive correlation coefficients with ash yield (with exceptions of Bi, Cs, Nb, Mn, Se, and Ti), are grouped in other four associations: Group C, Cr–V–Mo–U–Cd–Tl; Group D, Hg–Li–Sc–Ti–Eu–Nb–Cs–W; Group E, Bi–Sb; and Group F, Co–Ni–Cu–Pb–Zn–Mg–Se–Ca–Mn–S–Fe. The correlation coefficients of some elements, including Co, Cr, Cu, Fe, Hg, Li, Mo, Ni, P, S, Sc, U, V, and Zn, with ash yield are below the statistically significant value. Only Cr and Cu are negatively correlated to ash yield (−0.07 and −0.01, respectively), showing intermediate (organic and inorganic) affinity. Manganese and Fe are characterized by carbonate affinity probably due to high content of epigenetic veined ankerite in some coals. Phosphorus has low correlation coefficients with any other elements and is not included in these six associations. There are five possible genetic types of enrichment of elements in coal from western Guizhou Province: source rock, volcanic ash, low-temperature hydrothermal fluid, groundwater, and magmatic hydrothermal inputs.     

XRF AND INAA DETERMINATIONS OF MAJOR AND TRACE ELEMENTS IN GEOLOGICAL SURVEY OF JAPAN IGNEOUS AND SEDIMENTARY ROCK STANDARDS

Major and trace element analyses have been obtained by wavelength dispersive X-ray fluorescence for the Geological Survey of Japan Igneous rock series and selected samples from the Sedimentary rock series reference samples. Additional trace element data for the Igneous rock series were obtained by instrumental neutron activation analysis. Samples were analyzed multiple times for 10 major elements (with loss-on-ignition) and the following trace elements; As, Ba, Ce, Co, Cr, Cs, Cu, Eu, Ga, Hf, La, Lu, Nb, Nd, Ni, Pb, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Th, U, V, W, Y, Yb, Zn and Zr.     

Geochemistry of eocene calc-alkaline volcanic rocks from the Kastamonu area,Northern Turkey

Analytical data for Sr, Rb, Cs, Ba, Pb, rare earth elements, Y, Th, U, Zr, Hf, Sn, Nb, Mo, Ni, Co, V, Cr, Sc, Cu and major elements are reported for eocene volcanic rocks cropping out in the Kastamonu area, Pontic chain of Northern Turkey. SiO₂% versus K₂O% relationship shows that the analyzed samples belong to two major groups: the basaltic andesitic and the andesitic ones. High-K basaltic andesites and low-K andesites occur too. Although emplaced on continental type basement (the North Anatolian Crystalline Swell), the Pontic eocene volcanics show elemental abundances closely comparable with typical island arc calc-alkaline suites, e.g. low SiO₂% range, low to moderate K₂O% and large cations (Cs, Rb, Sr, Ba, Pb) contents and REE patterns with fractionated light and almost flat heavy REE patterns. REE and highly charged cations (Th, U, Hf, Sn, Zr) are slightly higher than typical calc-alkaline values. Ferromagnesian elements show variable values. Within the basaltic andesite group the increase of K%, large cations, REE, La/Yb ratio and high valency cations and the decrease of ferromagnesian element abundances with increasing SiO₂% content indicate that the rock types making up this group developed by crystalliquid fractionation of olivine and clinopyroxene from a basic parent magma. Trace element concentration suggest that the andesite group was not derived by crystal-liquid fractionation processes from the basaltic andesites, but could represent a distinct group of rocks derived from a different parent magma.     

酸性矿山排水影响的水库沉积物微量元素地球化学特征

为了解酸性矿山排水（AMD）影响下水库沉积物中微量元素的质量分数水平及其分布特征,对常年受酸性废水影响的贵州兴仁猫石头水库沉积物中26种微量元素的质量分数、相关性及控制因素进行了分析。结果表明：猫石头水库沉积物柱中Sr、Ba、Zr、V、Cr和As质量分数平均值超过了100 μg/g,其中As质量分数最高,平均值超过800 μg/g;Be、Ta、Co、Ag、Cd、Sn和Se质量分数的平均值都在5 μg/g以下;其他元素质量分数平均值则在10~60 μg/g之间。相较未受AMD影响的水系沉积物,研究区水库沉积物具有明显的As和Sb富集特征。水库沉积物中Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th之间存在显著正相关关系,而As与这些元素之间存在显著负相关关系。元素相关分析、因子分析及微量元素图解表明,Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th、Cr、Sb等元素受控于流域岩石化学风化和土壤物理侵蚀,这也是控制研究区元素分布最重要的因素,而Cu、Cd等重金属元素则与AMD对地层中元素的溶蚀析出和有机质等细颗粒物的吸附有关。另外,研究区重金属元素中,Cd、Cu、Pb、Cr、Zn的生态风险轻微,而As和Sb则具有很强的潜在生态风险。     

滇东南上二叠统吴家坪阶下部铝土矿 地球化学特征及物源分析

[摘 要] 滇东南地区上二叠统吴家坪阶下部铝土矿不整合于峨眉山玄武岩或灰岩之上,查明其物质来源对铝土矿勘探具有重要意义。对铝土矿及峨眉山大火成岩省玄武岩、花岗岩及下伏灰岩的地球化学指标进行研究,结果表明:滇东南铝土矿常量元素主要由SiO₂、Fe₂O₃、Al₂O₃、TiO₂ 和FeO 组成;铝土矿中富集Zr、Hf、Nb、Ta 元素,表明Zr、Hf、Nb、Ta 等高场强元素在滇东南地区铝土矿矿化过程中较为稳定,且Zr、Hf、Nb、Ta 表现出良好的相关性;铝土矿球粒陨石标准化曲线与峨眉山玄武岩配分曲线趋势一致,均富集轻稀土元素,而与下伏灰岩差异较大,且Zr-Hf、Nb-Ta 图解与峨眉山玄武岩呈线性关系,而与矮郎河过铝质花岗岩的相关性不强。据此推断滇东南地区上二叠统吴家坪阶下部铝土矿主要物质来源为峨眉山玄武岩。     

Seamount volcanism associated with the Xigaze ophiolite, Southern Tibet

Basaltic lavas at Renbu, Southern Tibet are associated with the Xigaze ophiolite in the Yarlung-Zangbo suture zone. They are alkaline lavas rich in large ion lithophile elements (LILE, Ba, Rb and Sr) and high field strength elements (HFSE, Nb, Ta, Zr and Hf), but poor in Cr, Co and Ni. All of the rocks have chondrite-normalized REE patterns enriched in light rare earth elements (LREE), comparable to modern basalts of the Society Islands, Kerguelen Plateau and Broken Ridge. Abundances of some immobile or moderately immobile elements (Nb, Ta, Zr, Hf, Y, Ti and REE) are also comparable to Kerguelen alkaline basalts. The Renbu basalts are geochemically similar to oceanic island basalts (OIB) and have some elemental ratios, such as Nb/Ta ratios = 15.7–18.1, Th/Nb =  0.06–0.10, La/Nb = 0.59–0.83 and Th/Ta = 1.03–1.52, similar to the primitive mantle. Their ⁸⁷Sr/⁸⁶Sr ratios (0.70453–0.70602) are relatively high, similar to OIB. In the ⁸⁷Sr/⁸⁶Sr vs. εNd(t) diagram, the Renbu basalts plot along a trend from N-MORB to EMII (enriched mantle II), suggesting the involvement of at least two mantle sources in their generation. The Renbu basalts represent seamount volcanism associated with the Xigaze ophiolite. They formed from an OIB-type mantle source within the Neo-Tethyan Ocean that had a composition similar to the modern Indian Ocean mantle.     

Extreme enrichment of Sb, Tl and other trace elements in altered MORB

We have analyzed 25 trace elements (e.g., Sb, Tl, Sn, rare earth elements (REE), Th, U, Nb, Pb, Zr, Hf, and Y) in altered mid-ocean ridge basalts (MORB) from locations near the mouth of the Gulf of California. Our results imply that the heavy REE and Y are not seriously affected by seawater alteration, in agreement with previous studies. The elements Zr, Hf, Nb, light REE and Sr are enriched up to a factor of 2 in some extremely altered samples. However, element ratios between Zr, Hf, and Nb (e.g., Zr/Hf, and Zr/Nb) are not greatly affected, presumably due to the chemical similarity of these elements during any exchange process. The enrichment of Th and Sn is even higher. Antimony, Tl, Cs, Rb, Rb, and Ba are most easily altered by water-rock interaction and are therefore the best indicators for seawater alteration. The enrichment factor of the most mobile element Sb is up to 2000.

There is a weak correlation between the concentration in seawater and the enrichment factors. On the other hand, the worldwide pelagic clay pattern matches the enrichment pattern much more closely, and the limited data available for local oceanic sediments give an even better correlation. A plausible model to explain the enrichment pattern may be an elemental exchange between basalt and seawater that had interacted earlier with overlying sediments.     

云南香格里拉春都斑岩体岩石地球化学特征研究

春都矿区复式斑岩体主要由闪长玢岩岩株及侵入其中的花岗闪长斑岩岩枝组成,后者为斑岩铜矿的成矿母岩。岩石地球化学特征表明,春都侵人岩属于钙碱性系列,cs、Rb、K、Ba、Sr等大离子亲石元素（LIL）在岩石中明显富集,Y、Hf、zr、Ti、Nb、Ta等较不活泼的高场强元素（HFS）则在岩石中相对亏损。通过构造环境图解判别,斑岩体形成于主动大陆边缘的火山弧构造环境,是甘孜．理塘洋壳向西俯冲的产物。     

Petrology and geochemistry of prograde deserpentinized peridotites from Happo-O’ne, Japan: Evidence of element mobility during deserpentinization

The prograde deserpentinized peridotites from the talc zone in the Happo-O’ne complex, central Japan, show differences in their field relation and mineral assemblage with the high-P retrograde peridotites of the other part of the complex. They show a mineral assemblage, olivine + talc + antigorite ± prograde tremolite ± chlorite, formed by thermal metamorphism around the granitic intrusion at T, 500-650 °C and P < 7 kbar. The olivine has numerous opaque inclusions and high Fo (91.5-96.5) relative to the retrograde olivine, reflecting its formation by deserpentinization. The prograde tremolite, which is low in Al₂O₃ (<1.0 wt.%), Cr₂O₃ (<0.35 wt.%), and Na₂O (<0.6 wt.%) but high in Mg# (up to 0.98) and SiO₂ (up to 59.9 wt.%), is different in size, shape and chemistry from the retrograde tremolite. The prograde peridotites display a U-shaped REE pattern (0.02-0.5 times PM), similar to diopside-zone retrograde metaperidotites, possible protoliths. They are enriched in LILE (e.g., Cs, Pb, Sr, Rb) relative to HFSE (e.g., Ta, Hf, Zr, Nb), like their protoliths, because of their local re-equilibration with the fluid released during dehydration of the protoliths. They have high contents of REE and some trace elements (e.g., Cs, Th, U, Ta) relative to their protoliths because of an external-element addition from the granitic magma. In-situ analyses of peridotitic silicates confirmed that the prograde tremolite and talc display a spoon-shaped primitive mantle (PM)-normalized REE pattern (0.1-3 times PM) in which LREE are higher than HREE contents. The prograde tremolite is depleted in Al, Na, Cr, Sc, V, Ti, B, HREE and Li, but is enriched in Si, Cs, U, Th, HFSE (Hf, Zr, Nb, Ta), Rb and Ba relative to the retrograde tremolite; the immobile-element depletion in this tremolite is inherited from its source (antigorite + secondary diopside), whereas the depletion of mobile elements (e.g., Li, B, Na, Al) is ascribed to their mobility during the deserpentinization and/or the depleted character of the source of tremolite. The enrichment of HFSE and LILE in the prograde tremolite is related to an external addition of these elements from fluid/melt of the surrounding granitic magma and/or in situ equilibrium with LILE-bearing fluid released during dehydration of serpentinized retrograde metaperidotites and olivine-bearing serpentinites (protoliths). The prograde olivine is higher in REE and most trace-element contents than the retrograde one due to the external addition of these elements; it is enriched in B, Co and Ni, but depleted in Li that was liberated during deserpentinization by prograde metamorphism.     

Clarkes of concentrations of trace elements in the Riphean fine-grained terrigenous rocks of the Uchur-Maya region and the Yenisei Range

The clarkes of concentrations (K_c) of a wide range of trace elements (Li, Be, B, Sc, V, Cr, Co, Ni, Cu, Zn, Ga, Ge, As, Rb, Sr, Y, Zr, Nb, Mo, Ag, Cd, In, Sb, Cs, Ba, REE, Hf, Ta, Hg, Tl, Pb, Bi, Th, and U) were analyzed for fine-gained terrigenous rocks (mudstones, metapelites) from the reference Riphean sections of the Uchur-Maya region and the Yenisei Range. It was established that the shales and mudstones of the Uchur and Aimchan groups in the Riphean hypostratotype section are characterized by moderate (2.5 < K_c < 5) and intense (K_c > 5) geochemical specialization for Li, B, and Zn. At the same time, the similar rocks of the Lakhanda and Ui groups do not exhibit any distinct geochemical specialization, although they are notably enriched in HREE. The metapelites from the basal formations of the Riphean sedimentary successions in the Yenisei Range are distinctly specialized for B and slightly for Li, Rb, Be, Nb, Ta, Th, Ge, and Cd. In addition, moderate specialization for Cu is characteristic of the metapelites from the Korda and Lopatino formations; for Bi, Sb, Hg, and V, for their analogs from the Potoskui Formation; and, for Hg and Cs, for the similar rocks from the Lopatino Formation. The metapelites of the Lower Riphean Korda Formation from the central zone of the Yenisei Range have elevated contents of significantly more elements (Li, Be, Sc, V, Cr, Co, Ni, Zn, As, Rb, Y, Zr, Nb, Sb, Ag, In, Hf, Hg, and others) than their counterparts from its eastern near-platform part. The mudstones of the ore-bearing (Pb, Zn) Gorevo Formation are characterized by elevated concentrations of several ore elements such as Pb, Cd, As, Sb, and Bi. The elevated K_c values of the rare lithophile and of several ore elements in the metapelites of the Yenisei Range are determined by the high geochemical differentiation of the Early Precambrian blocks constituting the western margin of the Siberian Craton, which were eroded in the Riphean, and the syn-sedimentary riftogenic and intraplate magmatism. On the contrary, the fine-grained and terrigenous rocks from the basal part of the Riphean section in the Uchur-Maya region are compositionally closer to the immature Late Archean substrates or their Early Proterozoic analogs.