橄榄岩—熔体相互作用过程中Re-Os体系的变化趋势: 对华北新生代地幔橄榄岩Re-Os年龄含义的启示

橄榄岩的Re-Os同位素体系作为探讨岩石圈地幔形成年龄的重要手段已受到人们越来越多的重视。然而,Re-Os体系是否会受到橄榄岩的低温蚀变如蛇纹石化和地幔交代作用或橄榄岩—熔体相互作用的影响并不十分清楚。本文在总结国际上典型造山带橄榄岩剖面研究和地幔橄榄岩捕虏体研究的基础上,发现橄榄岩的Re-Os同位素体系基本不受蛇纹石化等低温蚀变作用的影响; 但橄榄岩—熔体相互作用会造成橄榄岩的Re-Os体系的变化即Re或Os的带入。当熔体/岩石比例较小时(≤1),橄榄岩—熔体相互作用会造成橄榄岩的Re含量显著增加,而放射成因的Os同位素即¹⁸⁷Os增量有限。但当熔体/岩石比例很大时(≥1),会造成¹⁸⁷Os同位素显著增加。同时,橄榄岩的Re含量与中等程度不相容主、微量元素如Al、Ti、Yb的正相关关系可以通过橄榄岩的两阶段演化模式来解释,即早期的部分熔融残留和后期的橄榄岩—熔体相互作用共同影响的结果。橄榄岩的Re含量与Cr含量的正相关关系进一步说明了这一问题。上述结果对华北东部岩石圈地幔的演化过程有重要的启示作用。因为华北东部古生代时期的确存在太古宙岩石圈地幔,然而新生代时期地幔橄榄岩捕虏体普遍具有元古宙而非太古宙的事实证明橄榄岩—熔体的相互作用的确广泛存在,从而造成岩石圈地幔橄榄岩变年轻。因此,新生代地幔捕虏体的Re-Os同位素年龄并不是岩石圈地幔的形成年龄,而是混合作用的结果。汉诺坝地幔橄榄岩的Re含量和Sr、Nd同位素组成符合橄榄岩—多元熔体相互作用的混合趋势,其橄榄岩的全岩Al₂O₃含量和橄榄石Fo的反相关性能够通过橄榄岩—熔体相互作用来解释。     

Variscan ore formation and metamorphism at the Felbertal scheelite deposit (Austria): constraining tungsten mineralisation from Re–Os dating of molybdenite

The Felbertal scheelite deposit in the Eastern Alps has been regarded as the type locality for stratabound scheelite deposits. It is hosted by a Cambro-Ordovician metavolcanic arc sequence with minor Variscan granitoids (∼ 340 Ma) in the central Tauern Window. Re–Os model ages for molybdenite from the Felbertal tungsten deposit range between ∼ 358 and ∼ 336 Ma and record several pulses of magmatic-hydrothermal-metamorphic molybdenite formation. Molybdenite ages from the K2 orebody, a scheelite-rich quartz mylonite in the Western ore field, indicate that both mineralisation and mylonite are Variscan in age and suggest that the shear zone was active for ∼ 20 million years. Early stage tungsten mineralisation (Scheelite 1) in quartzitic ores in the Eastern ore field, which is free of molybdenite, yielded very low to near blank levels of Re and Os and thus could not be dated. However, molybdenite from scheelite–quartz stringers, previously interpreted as a feeder stockwork to quartzitic scheelite ore of presumed Cambrian age, yielded Variscan Re–Os ages of ∼ 342 and ∼ 337 Ma. Dating of molybdenite contained in scheelite ores thus far provides no indication of a Cambrian component to the tungsten mineralisation. Our data are consistent with a model of either granite intrusion-related ore formation and coeval metamorphic overprint during the Early Carboniferous or, alternatively, molybdenite formation may be exclusively attributed to Variscan metamorphism (see Stein 2006).     

Defining the Potential of Nanoscale Re‐Os Isotope Systematics Using Atom Probe Microscopy

Atom probe microscopy (APM) is a relatively new in situ tool for measuring isotope fractions from nanoscale volumes (< 0.01 μm³). We calculate the theoretical detectable difference of an isotope ratio measurement result from APM using counting statistics of a hypothetical data set to be ± 4δ or 0.4% (2s). However, challenges associated with APM measurements (e.g., peak ranging, hydride formation and isobaric interferences), result in larger uncertainties if not properly accounted for. We evaluate these factors for Re‐Os isotope ratio measurements by comparing APM and negative thermal ionisation mass spectrometry (N‐TIMS) measurement results of pure Os, pure Re, and two synthetic Re‐Os‐bearing alloys from Schwander et al. (2015, Meteoritics and Planetary Science, 50, 893) [the original metal alloy (HSE) and alloys produced by heating HSE within silicate liquid (SYN)]. From this, we propose a current best practice for APM Re‐Os isotope ratio measurements. Using this refined approach, mean APM and N‐TIMS ¹⁸⁷Os/¹⁸⁹Os measurement results agree within 0.05% and 2s (pure Os), 0.6–2% and 2s (SYN) and 5–10% (HSE). The good agreement of N‐TIMS and APM ¹⁸⁷Os/¹⁸⁹Os measurements confirms that APM can extract robust isotope ratios. Therefore, this approach permits nanoscale isotope measurements of Os‐bearing alloys using the Re‐Os geochronometer that could not be measured by conventional measurement principles.     

汇聚板块边缘岩浆中金属和氯的地球化学性质研究

总结了铜(Cu)、金(Au)、铼(Re)和氯(Cl)在汇聚板块边缘岩浆中的性质。在岛弧型的火山岩岩浆演化的早期,Cu、Au和Re均表现为中度不相容元素,含量随SiO2含量的增加而增加。在SiO2质量分数为58%时,多数岛弧型火山岩中Au、Cu的含量会突然大幅度下降。这一变化与铁和钛的变化是耦合的,铁和钛均由不相容元素变为相容元素,显示钛磁铁矿开始结晶了。进一步的研究表明,钛磁铁矿的结晶使硫酸根被还原为氢硫酸根,后者与Au、Cu形成氢硫酸根络合物,被萃取到流体相中,从而形成成矿流体。这一过程可以很好地解释Au、Cu矿床广泛分布于汇聚板块边缘的现象。与Au、Cu相反,Re的含量在SiO2质量分数为60%时才开始下降,而且是缓慢下降。这是因为Re通常比Au、Cu更亲石。此外,Re还具有强烈的挥发性。氯在东Manus岩浆中表现为高度不相容的特点。氯的性质主要受压力、初始水含量和岩浆演化分异程度的控制。计算结果显示,由于MORB和OIB含水量低,分异演化程度低,氯在上述岩浆中表现为高度不相容的特点。相比之下,氯在岛弧岩浆中的性质就复杂得多。随着水含量和岩浆房深度的不同,氯的性质可以从相容变到高度不相容。     

东秦岭地区钼矿床的铼-锇同位素年龄及其意义

金属矿床的成矿年龄多年来一直是矿床地质工作者关注的问题之一。中国地质科学院岩矿测试技术研究所建立的铼－锇同位素定年实验室，为研究钼矿床的形成时代提供了新的手段。因辉钼矿是最主要的含铼矿物之一，且基本上不含普通锇，其中所含＾１８７Ｏｓ是由＾１８７Ｒｅ衰变而来，故放射成因＾１８７Ｏｓ的积累是矿物年龄及铼含量的函数。本文采用同位素稀释－等离子体质谱法，测定了东秦岭钼矿带中几个不同类型的大型钼矿床的Ｒｅ－     

新疆香山铜镍硫化物矿床Re-Os同位素测定

通过对香山铜镍硫化物矿石中的镍黄铁矿进行Re-Os同位素测年,获得等时线年龄数据为(298±7．1)Ma。该数据表明产于东天山黄山—镜儿泉一带的这些铜镍硫化物矿床形成于晚石炭世—早二叠世,与该区广泛发育的造山型金矿、矽卡岩型银铜矿床和火山岩型铁铜矿床为同一时期的产物。其等时线~187Os/~188Os初始比值为0．682±0．32,γ_OS平均为444,表明在成矿过程及岩浆侵位期间有地壳物质加入成矿系统中。     

Ages of sediment-hosted Himalayan Pb–Zn–Cu–Ag polymetallic deposits in the Lanping basin,China: Re–Os geochronology of molybdenite and Sm–Nd dating of calcite

The Lanping basin is a significant Pb–Zn–Cu–Ag mineralization belt of the Sanjiang Tethyan metallogenic province in China. Over 100 thrust-controlled, sediment-hosted, Himalayan base metal deposits have been discovered in this basin, including the largest sandstone-hosted Pb–Zn deposit in the world (Jinding), and several Cu ± Ag ± Co deposits (Baiyangping, Baiyangchang and Jinman). These deposits, with total reserves of over 16.0 Mt Pb + Zn, 0.6 Mt Cu, and 7000 t Ag, are mainly hosted in Meso-Cenozoic mottled clastic rocks, and strictly controlled by two Cenozoic thrust systems developed in the western and eastern segments of the Lanping basin.To define the metallogenic history of the study area, we dated nine calcite samples associated with copper sulfides from the Jinman Cu deposit by the Sm–Nd method and five molybdenite samples from the Liancheng Cu–Mo deposit by the Re–Os method. The calcite Sm–Nd age for the Jinman deposit (58 ± 5 Ma) and the molybdenite Re–Os age for the Liancheng deposit (48 ± 2 Ma), together with previously published chronological data, demonstrate (1) the Cu–Ag mineralization in the western Lanping basin mainly occurred in three episodes (i.e., ∼56–54, 51–48, and 31–29 Ma), corresponding to the main- and late-collisional stages of the Indo–Asian orogeny; and (2) the Pb–Zn–Ag (±Cu) mineralization in the eastern Lanping basin lacked precise and direct dating, however, the apatite fission track ages of several representative deposits (21 ± 4 Ma to 32 ± 5 Ma) may offer some constraints on the mineralization age.     

浙江青田石平川钼矿控矿条件分析

石平川钼矿由燕山晚期第四次侵入碱性长石花岗岩体提供物源和热动力,火山机构、断裂和西山头组第二岩性段为成矿提供了导矿通道和容矿场所。     

安徽铜陵凤凰山夕卡岩型铜矿床中辉钼矿Re-Os同位素年龄及其地质意义

铜陵矿集区是我国长江中下游Cu-Au-Fe-Mo成矿带中最重要的有色金属基地之一,凤凰山矿床是铜陵矿集区的重要组成部分,为一个典型的夕卡岩型铜矿床。本文利用Re-Os同位素定年方法对凤凰山铜矿床进行了成矿时代测定,获得了辉钼矿的Re-Os同位素模式年龄范围为139.1±2.4～142.0±2.2Ma,等时线年龄为141.1±1.4Ma,与矿区内石英二长闪长岩和花岗闪长岩SHRIMP锆石U-Pb年龄(144.2±2.3Ma)相吻合,也与铜陵地区其他矿田的成矿时代基本一致,可能为岩石圈减薄事件的成矿响应。     

Geochronology and fluid inclusion study of the Yinjiagou porphyry–skarn Mo–Cu–pyrite deposit in the East Qinling orogenic belt,China

The Yinjiagou Mo–Cu–pyrite deposit of Henan Province is located in the Huaxiong block on the southern margin of the North China craton. It differs from other Mo deposits in the East Qingling area because of its large pyrite resource and complex associated elements. The deposit’s mineralization process can be divided into skarn, sulfide, and supergene episodes with five stages, marking formation of magnetite in the skarn episode, quartz–molybdenite, quartz–calcite–pyrite–chalcopyrite–bornite–sphalerite, and calcite–galena–sphalerite in the sulfide episode, and chalcedony–limonite in the supergene episode. Re–Os and ⁴⁰Ar–³⁹Ar dating indicates that both the skarn-type and porphyry-type orebodies of the Yinjiagou deposit formed approximately 143 Ma ago during the Early Cretaceous. Four types of fluid inclusions (FIs) have been distinguished in quartz phenocryst, various quartz veins, and calcite vein. Based on petrographic observations and microthermometric criteria the FIs include liquid-rich, gas-rich, H₂O–CO₂, and daughter mineral-bearing inclusions. The homogenization temperature of FIs in quartz phenocrysts of K-feldspar granite porphyry ranges from 341 °C to >550 °C, and the salinity is 0.4–44.0 wt% NaCl eqv. The homogenization temperature of FIs in quartz–molybdenite veins is 382–416 °C, and the salinity is 3.6–40.8 wt% NaCl eqv. The homogenization temperature of FIs in quartz–calcite–pyrite–chalcopyrite–bornite–sphalerite ranges from 318 °C to 436 °C, and the salinity is 5.6–42.4 wt% NaCl eqv. The homogenization temperature of FIs in quartz–molybdenite stockworks is in a range of 321–411 °C, and the salinity is 6.3–16.4 wt% NaCl eqv. The homogenization temperature of FIs in quartz–sericite–pyrite is in a range of 326–419 °C, and the salinity is 4.7–49.4 wt% NaCl eqv. The ore-forming fluids of the Yinjiagou deposit are mainly high-temperature, high-salinity fluids, generally with affinities to an H₂O–NaCl–KCl ± CO₂ system. The δ¹⁸O_H2O values of ore-forming hydrothermal fluids are 4.0–8.6‰, and the δD_V-SMOW values are between −64‰ and −52‰, indicating that the ore-forming fluids were primarily magmatic. The δ³⁴S_V-CDT values of sulfides range between −0.2‰ and 6.3‰ with a mean of 1.6‰, sharing similar features with deeply sourced sulfur, implying that the sulfur mainly came from the lower crust composed of poorly differentiated igneous materials, but part of the heavy sulfur came from the Guandaokou Group dolostone. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb values of sulfides are in the range of 17.331–18.043, 15.444–15.575, and 37.783–38.236, respectively, which is generally consistent with the Pb isotopic signature of the Yinjiagou intrusion, suggesting that the Pb chiefly originated from the felsic–intermediate intrusive rocks in the mine area, with a small amount of lead from strata. The Yinjiagou deposit is a porphyry–skarn deposit formed during the Mesozoic transition of a tectonic regime that is EW-trending to NNE-trending, and the multiepisode boiling of ore-forming fluids was the primary mechanism for mineral deposition.