蛇纹石化过程中铁活动性的高温高压实验研究

蛇纹石化过程中铁的活动性影响铁氧化物的形成和体系的氧逸度。然而,关于橄榄岩蛇纹石化过程中各矿物(橄榄石、斜方辉石和单斜辉石)蚀变过程中铁的活动性仍没有详细的研究。本文报道了80~200℃、饱和蒸气压下,不同的初始流体、水岩比条件下,橄榄岩蛇纹石化过程中铁的活动性。结果表明,蛇纹石化流体的铁含量较低(0.0~0.7mmol/kg),没有形成铁氧化物或铁氢氧化物,铁主要富集在蛇纹石和未反应的初始矿物中(例如,橄榄石和辉石)。由橄榄石蚀变形成的蛇纹石和由斜方辉石蚀变生成的蛇纹石化学组成相差较大,前者富铁而贫铝,后者贫铁而富铝。但当初始流体为碱性的0.5mol/L Na Cl(aq)时,两种不同来源的蛇纹石组成相差不大。尤为重要的是,单斜辉石蚀变生成的蛇纹石铁含量较高,8.1%~10.2%Fe O,远高于单斜辉石的铁含量(2.6%Fe O)。以上表明,低温蛇纹石化过程中,铁不能够大规模、长距离的运移,但在微米尺度上是活动的。     

橄榄岩蛇纹石化过程中氢气和烷烃的形成

蛇纹石化过程中形成氢气、烷烃和有机酸,为海底热液区生命活动提供物质和能量来源,可能对地球和其他行星早期生命起源和演化有重要影响。目前关于蛇纹石化过程中氢气和烷烃形成的研究大多以橄榄石为初始物,且温度和压力较低(≤300℃,500bar)。本研究通过一系列的水热实验,研究300~500℃、1~3kbar时橄榄石、斜方辉石、单斜辉石、橄榄岩、玄武岩以及玄武岩与橄榄岩混合物发生蛇纹石化反应后氢气和烷烃的生成。300℃、3kbar时,橄榄石蛇纹石化后产生的氢气远大于辉石蚀变后产生氢气的量。随着温度的增加,400~500℃、3kbar时,橄榄石蚀变程度极低,产生氢气的量低于斜方辉石。单斜辉石实验后没有发生蚀变,不产生氢气和烷烃。400~500℃、3kbar时,橄榄岩蛇纹石化后产生的氢气和烷烃远高于橄榄石、斜方辉石和单斜辉石。玄武岩蛇纹石化后生成氢气和甲烷的量低于橄榄岩,但与玄武岩和橄榄岩混合物相当。这是因为玄武岩的单斜辉石蚀变后形成富铁的透辉石(~8.1%FeO),透辉石的Fe以Fe2+为主,这降低了Fe3+和氢气的量。以上表明,橄榄岩的蛇纹石化不同于橄榄石和斜方辉石。不仅是海底热液蚀变产生氢气和甲烷,洋壳俯冲过程中地幔楔橄榄岩蛇纹石化也会生成氢气和甲烷,但由于洋壳玄武岩的加入,氢气和甲烷的量会远小于橄榄岩蚀变时的量。     

大洋橄榄岩的蛇纹石化过程:从海底水化到俯冲脱水SCIEI北大核心CSCD

蛇纹石化是海底最重要的水岩相互作用之一,指基性岩和超基性岩中的橄榄石和辉石等镁铁质矿物在相对低温条件下发生水热蚀变产生蛇纹石等矿物的热液变质作用。蛇纹石族矿物主要有三种,分别是利蛇纹石、纤蛇纹石和叶蛇纹石。低温状态蛇纹石族矿物主要以利蛇纹石和纤蛇纹石的形式存在,高温状态下主要以叶蛇纹石的形式存在。影响大洋蛇纹石化过程的因素不容忽视,温度、氧化还原程度、pH值、水岩比(W/R)等都在其中扮演着重要的角色。总的来说,地幔物质易出露在地壳减薄区域和断裂构造处,这有利于与流体充分接触反应,从而决定了大洋蛇纹石化作用发生的可能位置。对蛇纹石化程度的描述,当前人们大多通过岩石微观结构、地球化学指标来定性指示,磁学指标有望实现对蛇纹石化程度的定量解释。蛇纹石化作用对海底磁异常、地球生命演化进程、成矿作用等都有一定的贡献。此外,俯冲带脱水及弧岩浆的形成都与之有联系。总之,基性与超基性岩石蛇纹石化与俯冲带蛇纹岩脱水过程是地球水循环过程的重要机制,但未来揭示蛇纹岩的磁学性质和俯冲变质过程,仍需进一步探索。     

蛇纹石化和俯冲带蛇纹岩变质脱水过程中流体活动性元素的行为

蛇纹石是大洋岩石圈和俯冲带内水和流体活动性元素最重要的载体之一。研究蛇纹石化和蛇纹岩变质脱水过程中流体活动性元素的行为是认识俯冲带元素地球化学循环的关键。蛇纹岩是指主要由蛇纹石类矿物构成的岩石,包括利蛇纹石、纤蛇纹石和叶蛇纹石。蛇纹石化过程中会造成流体活动性元素(B、Li、As、Sb、Pb、Cs、U、Sr和Ba等)的显著富集,并且由于原岩性质、流体成分和氧逸度等条件的不同,大洋岩石圈蛇纹岩和弧前蛇纹岩的特征也略有不同。例如,弧前蛇纹岩具有相对高的As、Sb、B和相对低的U,这反映了俯冲沉积物来源流体的贡献。在俯冲带蛇纹岩的变质脱水过程中,利蛇纹石向叶蛇纹石的转变伴随着矿物内超过50%F和Cl的释放,以及一些流体活动性元素(如B和Li)的迁出;此外,蛇纹石分解形成的变质橄榄石中的流体包裹体指示,蛇纹石脱水分解所产生的流体具有高于原始地幔几个数量级的Cl、Cs、Pb、As、Sb、Ba、Rb、B、Sr、Li和U含量。由于利蛇纹石中的Fe~(3+)含量较叶蛇纹石高,这种矿物相转变过程中也伴随着俯冲通道内的一系列氧化还原过程,从而影响流体性质和新形成的叶蛇纹石的成分。蛇纹岩与岛弧岩浆在流体活动性元素富集规律上的相似性说明蛇纹岩在俯冲带元素循环中扮演着重要的角色。此外,蛇纹石矿物相转变过程中F、Cl、B等元素的释放,可能对于斑岩型金矿、蛇绿岩中的金矿和某些蛇纹岩作为赋矿围岩的硼矿的形成起到重要的作用。     

藏北昂吾地区超基性岩的蛇纹石化和磁铁矿化过程及影响因素

班公湖-怒江缝合带广泛分布超基性岩及蛇纹石化超基性岩,已有研究表明它们与区域成矿关系密切,其蛇纹石化过程使一些元素活化并具有一定的成矿潜力。位于班-怒带中段的昂吾地区蛇纹石化超基性岩主要矿物成分有橄榄石、单斜辉石、铬铁矿、利蛇纹石、磁铁矿和绿泥石等,原岩恢复表明该超基性岩为单辉橄榄岩。镜下鉴定、背散射电子图像、能谱成分分析和电子探针分析结果显示单辉橄榄岩的蛇纹石化及蚀变过程可分为三个阶段:(Ⅰ)以形成相对富铁蛇纹石(Mg#=75～88)为主,基本无磁铁矿析出;(Ⅱ)形成相对富镁的蛇纹石(Mg# 90),析出磁铁矿;(Ⅲ)蛇纹石进一步蚀变成绿泥石。热力学模拟及多组分矿物相平衡图表明,在蛇纹石化过程中,昂吾地区超基性岩中的辉石脱硅致使反应体系SiO_2活度升高,限制了磁铁矿的生成。同时也发现,在利蛇纹石稳定存在的温度区间内(100～300℃),本研究的蛇纹石化体系温度倾向高值区,不利于磁铁矿的析出。进而探讨了原岩成分、反应体系SiO_2活度及温度等因素对蛇纹石化过程中磁铁矿析出的影响。本研究有助于理解班-怒带内超基性岩的蛇纹石化过程及磁铁矿化机制。     

西藏雅鲁藏布江缝合带东段泽当地幔橄榄岩特征及其意义

泽当岩体位于雅鲁藏布江缝合带东段,主要由地幔橄榄岩、辉长辉绿岩和基性火山岩等组成。地幔橄榄岩主要为方辉橄榄岩和二辉橄榄岩,有少量透镜状纯橄岩。地幔橄榄岩经历了强烈的塑性变形作用。地幔橄榄岩中橄榄石的Fo值为89.6~91.8,属镁橄榄石;斜方辉石为顽火辉石,En 87.8~90.3;单斜辉石En 44.1~50.0,主要为顽透辉石和透辉石。铬尖晶石的Cr#值(=100×Cr/(Cr+Al))为17.0~93.6,其中,二辉橄榄岩和方辉橄榄岩中的铬尖晶石为富铝型尖晶石,纯橄岩中的铬尖晶石Cr#最高,为富铬型尖晶石。地幔橄榄岩的部分熔融程度为17%~34%,表明泽当地幔橄榄岩可能经历了多阶段的过程。亏损的主量元素组成和低于原始地幔的稀土元素含量(0.15×10-6~0.61×10-6)指示泽当地幔橄榄岩为经历过部分熔融和熔体抽取的亏损残余地幔岩石。REE配分型式为中稀土亏损的"V"型或"U"型,原始地幔标准化元素比值(La/Sm)N为0.5~8.0,表明泽当地幔橄榄岩经历过交代作用。矿物化学与地球化学数据表明泽当地幔橄榄岩形成于MOR环境,后受到SSZ环境的改造。     

A chlorine isotope study of DSDP/ODP serpentinized ultramafic rocks: Insights into the serpentinization process

Eight DSDP/ODP cores were analyzed for major ion concentrations and δ³⁷Cl values of water-soluble chloride (δ³⁷Cl_WSC) and structurally bound chloride (δ³⁷Cl_SBC) in serpentinized ultramafic rocks. This diverse set of cores spans a wide range in age, temperature of serpentinization, tectonic setting, and geographic location of drilled serpentinized oceanic crust. Three of the cores were sampled at closely spaced intervals to investigate downhole variation in Cl concentration and chlorine isotope composition.The average total Cl content of all 86 samples is 0.26 ± 0.16 wt.% (0.19 ± 0.10 wt.% as water-soluble Cl (X_WSC) and 0.09 ± 0.09 wt.% as structurally bound Cl (X_SBC)). Structurally bound Cl concentration nearly doubles with depth in all cores; there is no consistent trend in water-soluble Cl content among the cores. Chlorine isotope fractionation between the structurally bound Cl⁻ site and the water-soluble Cl⁻ site varies from − 1.08‰ to + 1.16‰, averaging to + 0.21‰. Samples with negative fractionations may be related to reequilibration of the water-soluble chloride with seawater post-serpentinite formation. Six of the cores have positive bulk δ³⁷Cl values (+ 0.05‰ to + 0.36‰); the other two cores (173-1068A (Leg-Hole) and 84-570) have negative bulk δ³⁷Cl values (− 1.26‰ and − 0.54‰). The cores with negative δ³⁷Cl values also have variable Cl⁻ / SO₄² ratios, in contrast to all other cores. The isotopically positive cores (153-920D and 147-895E) show no isotopic variation with depth; the isotopically negative core (173-1068A) decreases by ∼1‰ with depth for both the water-soluble and structurally bound Cl fractions.Non-zero bulk δ³⁷Cl values indicate Cl in serpentinites was incorporated during original hydration and is not an artifact of seawater infiltration during drilling. Cores with positive δ³⁷Cl values are most likely explained by open system fractionation during hydrothermal alteration, with preferential incorporation of ³⁷Cl from seawater into the serpentinite and loss of residual light Cl back to the ocean. Fluid / rock ratios were probably low as evidenced by the presence of water-soluble salts. The two isotopically negative cores are characterized by a thick overlying sedimentary package that was in place prior to serpentinization. We believe the low δ³⁷Cl values of these cores are a result of hydration of ultramafic rock by infiltrating aqueous pore fluids from the overlying sediments. The resulting serpentinites inherit the characteristic negative δ³⁷Cl values of the pore waters. Chlorine stable isotopes can be used to identify the source of the serpentinizing fluid and ultimately discern chemical and tectonic processes involved in serpentinization.     

汉诺坝幔源橄榄岩包体的微量元素和Re-Os同位素地球化学：SCLM的性质和形成时代

本文报道了汉诺坝新生代碱性玄武岩中地幔橄榄岩包体的主量、微量元素和Re-Os同位素。14个尖晶石橄榄岩Re、Os含量分别为0.022～0.193ng/g和1.237～4.304ng/g，^187Os/^188Os比值为0.1183～0.1244，与^187Os/^188Os比值相关性不好，但与熔体亏损指标如重稀土元素Yb的含量、全岩Al2O3的百分含量有很好的线性关系，可能反映了地幔熔融后的Re或/和Os的活动。全岩Al2O3、CaO、TiO2含量均与MgO有很好的负相关性，全岩原始地幔标准化REE丰度模式呈现了LREE亏损，表明该区橄榄岩包体是由软流圈地幔经过部分熔融，亏损了玄武质组分后形成的。由Os同位素代理等时线得到该区陆下岩石圈地幔的形成年龄为1.7～2.0Ga，表明尖晶石相橄榄岩所代表的岩石圈地幔是中元古代的陆下岩石圈地幔减薄后的残留体。     

Estimation of surface iron oxide abundance with suppression of grain size and topography effects

Mineral forms of iron oxide, such as hematite, goethite and jarosite, are important because they are widely distributed at the Earth’s surface and because they are used as indicators for mineral exploration. Iron oxide abundance in rocks containing these minerals can be estimated from the absorption depth at wavelengths of around 900 nm in a reflectance spectrum, but this depth is also affected by extraneous factors such as grain size and topography. This paper investigated the effect of grain size on reflectance spectra and proposed a method for estimating iron oxide abundance in surface rocks by using remotely sensed data with suppression of the effects of grain size and topography. Reflectance spectra were measured in a laboratory from rock powder samples of different grain sizes containing iron oxide minerals. While the reflectance increased with decreasing grain size, the presence of ferric iron caused the absorption depth to be almost constant at around 900 nm, irrespective of the chemical composition of the sample. In addition, the difference between the reflectance at 550 nm and 760 nm (Slope) was a function of grain size. Iron oxide abundance can be estimated accurately by MCR-900D, which is the maximum absorption depth at the absorption center after the effect of grain size and topography was suppressed by Slope and the continuum-removal method, which takes the ratio between the original spectrum and its continuum, respectively. Correlation of MCR-900D results with datasets of actual spectral and chemical iron oxide laboratory measurements revealed that the mineral forms also need to be considered. MCR-900D results were significantly correlated with rock samples classified as containing different forms of iron oxide minerals (hematite, goethite and jarosite). Finally, MCR-900D was applied to an AVIRIS dataset for the Cuprite site in Nevada, USA. The results represented the enrichment zones of iron oxide within hydrothermally altered areas.     

华北克拉通西北部显生宙岩石圈地幔属性与演化特征: 橄榄岩捕虏体证据

众所周知,华北克拉通东部岩石圈地幔的组成和性质在显生宙发生了显著变化,但由于西部出露含有捕虏体的火山岩较少,这在一定程度上限制了人们对该区岩石圈地幔属性与演化特征的认识。本文将华北克拉通西北部晚白垩世-新生代玄武岩中橄榄岩捕虏体的研究成果归纳总结,旨在进一步揭示该区岩石圈地幔的属性与演化特征。研究表明,华北克拉通西北部岩石圈地幔主要由低Mg^#的二辉橄榄岩和少量高Mg^#的方辉橄榄岩组成。高Mg^#橄榄岩代表该区受轻微再富集作用影响的古老岩石圈地幔残余,低Mg^#橄榄岩是软流圈来源熔体与高Mg^#橄榄岩反应的产物,代表地幔再富集作用对古老岩石圈地幔改造的结果。该区岩石圈地幔经历了多期地幔交代作用的改造,早期交代事件与古亚洲洋俯冲有关,近期与软流圈来源的玄武质熔体有关。这种广泛的地幔再富集作用对华北克拉通古老岩石圈地幔的转变做出了重要贡献。

     

Refertilization of ancient lithospheric mantle beneath the central North China Craton: Evidence from petrology and geochemistry of peridotite xenoliths

The petrology and geochemistry of peridotite xenoliths in the Cenozoic basalts from Fanshi, the central North China Craton (NCC), provide constraints on the evolution of sub-continental lithospheric mantle. These peridotite xenoliths are mainly spinel-facies lherzolites with minor harzburgites. The lherzolites are characterized by low forsterite contents in olivines (Fo < 91) and light rare earth element (LREE) enrichments in clinopyroxenes. In contrast, the harzburgites are typified by high-Fo olivines (> 91), high-Cr# spinels and clinopyroxenes with low abundances of heavy REE (HREE). These features are similar to those from old refractory lithospheric mantle around the world, and thus interpreted to be relics of old lithospheric mantle. The old lithospheric mantle has been chemically modified by the influx of melts, as evidenced by the Sr–Nd isotopic compositions of clinopyroxenes and relatively lower Fo contents than typical Archean lithospheric mantle (Fo > 92.5). The Sr–Nd isotopic compositions of harzburgites are close to EM1-type mantle, and of the lherzolites are similar to bulk silicate earth. The latter could be the result of recent modification of old harzburgites by asthenospheric melt, which is strengthened by fertile compositions of minerals in the lherzolites. Therefore, the isotopic and chemical heterogeneities of the Fanshi peridotite xenoliths reflect the refertilization of ancient refractory lithospheric mantle by massive addition of asthenospheric melts. This may be an important mechanism for the lithospheric evolution beneath the Central NCC.     

Lithospheric mantle beneath the south-eastern Siberian craton: petrology of peridotite xenoliths in basalts from the Tokinsky Stanovik

We provide petrographic, major and trace element data for over 30 spinel peridotite xenoliths from the Tokinsky Stanovik (Tok) volcanic field on the Aldan shield to characterize the lithospheric mantle beneath the south-eastern margin of the Siberian craton, which formed in the Mesoproterozoic. High equilibration temperatures (870–1,010°C) of the xenoliths and the absence of garnet-bearing peridotites indicate a much thinner lithosphere than in the central craton. Most common among the xenoliths are clinopyroxene-poor lherzolites and harzburgites with Al₂O₃ and CaO contents nearly as low as in refractory xenoliths from kimberlite pipes (Mir, Udachnaya) in the central and northern Siberian craton. By contrast, the Tok peridotites have higher FeO, lower Mg-numbers and lower modal orthopyroxene and are apparently formed by shallow partial melting (3 GPa). Nearly all Tok xenoliths yield petrographic and chemical evidence for metasomatism: accessory phlogopite, amphibole, phosphates, feldspar and Ti-rich oxides, very high Na₂O (2–3.1%) in clinopyroxene, LREE enrichments in whole-rocks.Electronic Supplementary Material Supplementary material is available for this article at     

松辽盆地南部岩石圈地幔变形特征及各向异性分析——来自橄榄岩包体的约束

SKS测量结果显示松辽盆地快波方向分布较为复杂, 由于缺乏深部岩石变形资料约束, 制约了地震波各向异性成因解释。本文通过对松辽盆地南部双辽地区橄榄岩包体进行详细的岩石学、地球化学、显微结构、各向异性研究, 结果显示双辽地区橄榄岩包体的平衡温度为893~1152℃, 来源于岩石圈地幔。橄榄岩中橄榄石的晶格优选方位(CPO)类型主要为A型、D型和AG型, 其中, AG型和D型CPO可能形成于西太平洋板块向欧亚大陆俯冲回撤导致的岩石圈变形, AG型橄榄石CPO也可能形成于熔体存在下的橄榄石变形。基于CPO计算获得的橄榄岩包体全岩V_P各向异性(AV_P)为4.79%~11.80%, 最大剪切波各向异性(AV_Smax)为3.13%~7.93%。结合地球物理测量结果, 推断松辽盆地南部复杂的SKS各向异性的主要贡献可能来源于面理陡倾或直立的岩石圈地幔。

     

The legacy of crystal-plastic deformation in olivine: high-diffusivity pathways during serpentinization

Crystal-plastic olivine deformation to produce subgrain boundaries composed of edge dislocations is an inevitable consequence of asthenospheric mantle flow. Although crystal-plastic deformation and serpentinization are spatio-temporally decoupled, we identified compositional readjustments expressed on the micrometric level as a striped Fe-enriched ( [`(X)]<sub>\textFe</sub> \bar{X}_{\text{Fe}}  = 0.24 ± 0.02 (zones); 0.12 ± 0.02 (bulk)) or Fe-depleted ( [`(X)]_\textFe \bar{X}_{\text{Fe}}  = 0.10 ± 0.01 (zones); 0.13 ± 0.01 (bulk)) zoning in partly serpentinized olivine grains from two upper mantle sections in Norway. Focused ion beam sample preparation combined with transmission electron microscopy (TEM) and aberration-corrected scanning TEM, enabling atomic-level resolved electron energy-loss spectroscopic line profiling, reveals that every zone is immediately associated with a subgrain boundary. We infer that the zonings are a result of the environmental Fe²⁺Mg₋₁ exchange potential during antigorite serpentinization of olivine and the drive toward element exchange equilibrium. This is facilitated by enhanced solid-state diffusion along subgrain boundaries in a system, which otherwise re-equilibrates via dissolution-reprecipitation. Fe enrichment or depletion is controlled by the silica activity imposed on the system by the local olivine/orthopyroxene mass ratio, temperature and the effect of magnetite stability. The Fe-Mg exchange coefficients K_\textD^{\textAtg/\textOl} K_{\text{D}}^{{{\text{Atg}}/{\text{Ol}}}} between both types of zoning and antigorite display coalescence toward exchange equilibrium. With both types of zoning, Mn is enriched and Ni depleted compared with the unaffected bulk composition. Nanometer-sized, heterogeneously distributed antigorite precipitates along olivine subgrain boundaries suggest that water was able to ingress along them. Crystallographic orientation relationships gained via electron backscatter diffraction between olivine grain domains and different serpentine vein generations support the hypothesis that serpentinization was initiated along olivine subgrain boundaries.     

The Bizielle vein (valle de Gistain): A case of iron oxide transformations at the Pyrenees of Spain

The Bizielle vein has some unique features among the Pyrenean alpine veins that allow us to address the question of the nature of iron oxides transformations under low temperature hydrothermal conditions, which is well known to prevailed over wide areas of western Europe between early Triassic to early Cretaceous times. Isotopic studies indicate a deep-seated origin of the ore-forming fluids and suggest that the metals were leached from the Variscan basement (mainly from granites). Isotopic geothermometry and regional evidences point to a 250 °C and reducing fluid, being SH₂ the predominant S specie. Under such conditions, the proposed in situ deposition of hematite is a consequence of Fe carbonates dissolution and oxidation involving dissolution/precipitation processes in the sense of Putnis. Non-redox model is a quite plausible origin for subsequent hematite to magnetite conversion.     

西藏雅鲁藏布江缝合带的普兰地幔橄榄岩中发现金刚石:蛇绿岩型金刚石分类的提出

西藏罗布莎蛇绿岩的地幔橄榄岩和铬铁矿中发现金刚石和特殊矿物群引发了新的问题,罗布莎地幔橄榄岩含特殊地幔矿物是不是一个孤立的特殊现象,或这是一个普遍存在的规律?显然,这是一个至关重要的问题.本文报道在雅鲁藏布江缝合带西段,距离罗布莎1000km以远的普兰蛇绿岩的地幔橄榄岩中发现与罗布莎类似的金刚石和特殊地幔矿物群.普兰的地幔橄榄岩体主体为方辉橄榄岩,含少量的纯橄岩和二辉橄榄岩,研究表明,属典型MOR型亏损地幔橄榄岩.通过分选,在657kg的地幔橄榄岩大样中发现了金刚石和碳硅石等30余种矿物的特殊矿物群,包括自然铬、自然铁和自然锌等强还原条件下形成的单质元素矿物.该矿物群与罗布莎地幔橄榄岩和铬铁矿中发现的特殊矿物群十分相似,表明罗布莎的地幔橄榄岩不是雅鲁藏布江缝合带中的一个特例.结合在俄罗斯乌拉尔Ray-Iz铬铁矿中发现类似的矿物群,以及世界其他地区的有关阿尔卑斯型地幔橄榄岩中金刚石的报道,认为蛇绿岩地幔橄榄岩中可能普遍含有金刚石,并将蛇绿岩地幔橄榄岩中产出的金刚石归为一种新的金刚石产出类型,即蛇绿岩型金刚石,不同于金伯利岩型金刚石和超高压变质带中产出的变质金刚石类型.     

Implications of Pb isotope signatures of rocks and iron oxide Cu-Au ores in the Candelaria-Punta del Cobre district,Chile

Lead isotope ratios of ores of the Candelaria-Punta del Cobre iron oxide Cu-Au deposits and associated Early Cretaceous volcanic and batholithic rocks have been determined. For the igneous rocks, a whole-rock acid attack technique based on the separate analyses of a leachate and the residual fraction of a sample was used. The lead isotope systematics of leachate–residue pairs are significantly different for unaltered and altered igneous rocks of the Candelaria-Punta del Cobre district. Residues of unaltered igneous rocks likely represent the common lead. In contrast, residues of all the altered igneous rocks except two samples have higher Pb isotope ratios than those of unaltered magmatic rocks and cannot represent common lead. We suggest that this is a result of the hydrothermal alteration suffered by these rocks and that the common lead composition of the altered igneous (volcanic and plutonic) rocks must have been similar to that of the unaltered batholith rocks. The conclusion that the altered volcanic rocks originally had a similar common lead isotope composition as the batholith is consistent with geological and geochemical arguments (e.g., setting, regional geologic evolution, ages and relative distribution of volcanic and intrusive rocks, magmatic affinities), which indicate that these rocks were derived from similar Early Cretaceous parent magmas. The modification of the leachate–residue pair lead isotope systematics of most altered igneous rocks is consistent with a selective removal of lead and uranium from these rocks by an oxidized hydrothermal fluid. The result of the hydrothermal leaching has been to alter magmatic rocks in a way that (1) their leachable fraction is presently a mix of common lead similar to that of the ore event and of radiogenic lead evolved from a source with a consistently high Th/U, and that (2) their residual fraction has less common lead than unaltered rocks. The outcrop area with altered volcanic rocks displaying anomalously high lead isotope ratios extends over 25 km along the eastern margin of the batholith. Since lead of the ores in the Candelaria-Punta del Cobre district has the same isotopic composition as the common lead of unaltered magmatic rocks of the area, the lead isotope data are consistent with a derivation of the ore lead (and by inference of other metals like Cu) both directly from a magmatic fluid exsolved during crystallization of the batholith and/or from hydrothermal leaching of the volcanic rocks originally having similar isotopic compositions as the batholith.Editorial handling: B. Lehmann     

Intracellular and extracellular mineralization of a microbial community in the Edmond deep-sea vent field environment

Microbial biomineralization in submarine hydrothermal environments provides an insight into the formation of vent microfossils and the interactions between microbes, elements and minerals throughout the geological record. Here, we investigate microbial biomineralization of a deep-sea vent community in the Edmond vent field and provide ultrastructural evidence for the formation of microfossils and biogenic iron-rich minerals related to Archaea and Bacteria. Environmental scanning electron microscopy (ESEM) analysis shows that filamentous and spiral microbes are encrusted by a non-crystalline silica matrix and minor amounts of iron oxides. Examination by transmission electron microscopy (TEM) reveals acicular iron-rich particles and aggregates that occur either intracellularly or extracellularly. A culture-independent molecular phylogenetic analysis demonstrates a diverse range of Bacteria and Archaea, the majority of which are related to sulfur metabolism in the microbial mats. Both Archaea and Bacteria have undergone silicification, in a similar manner to microorganisms in some terrestrial hot springs and indicating that silicification may be driven by silica supersaturation and polymerization. Formation mechanisms of intracellular and extracellular iron oxides associated with microbes are discussed. These results enhance our understanding of microbial mineralization in extreme environments, which may be widespread in the Earth's modern and ancient hydrothermal vent fields.     

Source constraints for the young basaltic rocks from the northernmost end of Cappadocian region,Turkey: Melting evidence from peridotite and pyroxenite source domains

Widespread magmatic activity developed in the Middle Miocene in the Cappadocian Region of Central Anatolia in Turkey. Despite several previous studies that focus on the geochemical features of the magmatic rocks, the source components and development of melting conditions are still a matter of debate.Recent basaltic rocks from Karaburna and Gül?ehir (1228 and 96 Ka, respectively, Dogan, 2011) are considered as a part of the Central Anatolian Volcanic Province, situated at the northernmost end of the Cappadocian Region. These lavas have similar large ion lithophile (LIL) (except Rb) and high field strength (HFS) element abundances, however, Karaburna samples are more enriched in HFS elements, and both of the rocks suites reflect HFS depletions relative to the OIB signature.Karaburna and Gül?ehir basalts have low Nb/La (0.45–0.5; 0.35–0.5), Nb/Th (2.75–4.61; 1.26–2.85) values, respectively, suggesting contributions from crustal sources, whereas Zr/Ba ratios of these samples range between 0.32–0.93 and 0.4–0.88 and imply that these rocks appear to be derived from asthenospheric sources. These incompatible element ratios can be attributed to either different geochemical processes, or are related to melting from different source component(s).The ambient mantle source of the Cappadocian region appears to be consistent with spinel peridotite, but this domain is not solely satisfactory to represent the melting conditions in the light of new elemental data. Values of Tb/Yb(N) and Zn/Fe provide new constraints suggesting the magmas were generated from the asthenosphere. Tb/Yb(N) ratio separates garnet – spinel transition Tb/Yb_(N) (>1.8) and Zn/Fe ratio displays separation between the peridotite-derived (Zn/Fe <12) and pyroxenite-derived (13?20) melts.A melting model based on REE ratios and Zn/Fe, Co/Fe, Tb/Yb(N) values indicates that basaltic rocks were not derived from a single source component (peridotite). Instead, those values suggest substantial melting contributions from a pyroxenite source domain, which has not been discussed as a source component in previous studies. Melts, from both of the source domains, with the result of asthenospheric upwelling linked to the downgoing Aegean and Cyprean slabs, are distinct from the alkaline character frequently observed as the final products of recent volcanic activity in the Cappadocian region and also explains the different trace element variations observed in such a small scale.     

碱熔除铁氟化物置换容量法测定铁矿石中的三氧化二铝

试样经氢氧化钠碱熔,过滤分离铁等元素,将滤液酸化、DETA络合、氟化钠置换,再用硫酸铜标准溶液回滴释放出来的EDTA,从而实现对铝的测定,通过本方法对铁矿石标准物质及样品的测定,结果的相对标准偏差在0.93%~2.95%之间,且铁矿石标准物质测定值与认定值相符。