大洋多金属结核同位素地球化学研究

本文对DY85-1航次采自东太平洋海盆“CC”区不同地貌区、不同类型的大洋多金属结核进行了O、C、H、Si等同位素综合研究。结果表明,O同位素变化能反映结核的生成环境、生长速率、物质来源及成矿机理;Si同位素组成特征能帮助推测结核核心物质的来源;C同位素的研究表明,多金属结核成矿作用是在古海洋水变冷的总趋势下进行的;δ13C、δ18O和δD的规律变化,反映了海洋水变冷的周期性和渐变性。     

安徽铜陵天马山硫金矿床物质来源探讨

天马山硫金矿床的矿体分为层状 和穿层矿体。接触带矿体是典型的夕卡岩型。层状和穿层矿体受石岩系黄龙组、船山组地层层位和层间断裂控制。铅、硫同位素组成等资料表明,其形成经历了同生沉积和岩浆热液叠加、改造两种性质不同的成矿富集过程。金等金属成矿物质主要来源于岩浆,砷主要来源于地层,硫来源于地层和岩浆。     

硼同位素及其地质应用研究

硼的两个稳定同位素（10B 和11B）相对质量差较大,因此,硼同位 素分馏较显著。由于分析测量技术方面的改进和创新, 硼同位素地球化学近年来有了长足 的发展。业已查明,自然界中δ11B值变化为 －37‰～+58‰。其中,较负的 δ11B值见于非海相蒸发硼酸盐矿物和某些电气石,而较正的δ11B值见 于某些盐湖卤水和蒸发海水。现代大洋水的δ11B值十分恒定 (+39,5‰)。原始 地幔的δ11B值估测为－10‰±2‰。陨石的δ11B值很不均一,变化 可达90‰。而月岩的δ11B值变化较小（－6‰～+4‰）。由于硼同位素存在大的 分馏和不同地质体中截然不同的δ11B值,硼同位素地质应用范围十分广泛。目 前,硼同位素在研究星云形成过程和宇宙事件,壳-幔演化和板块俯冲作用过程,判别沉积 环境,研究矿床成因,示踪古海洋和古气候条件,和判断环境污染源区等方面的研究中成效显著。     

白云鄂博富稀土元素碳酸岩墙的 碳和氧同位素特征

重点解剖了一条距白云鄂博超大型REE-Nb-Fe矿床东矿北东方向2 k m、切割白云鄂 博群H1及H3岩性段的细粒方解石碳酸岩岩墙的碳和氧同位素地球化学特征。结果表明,碳酸 岩的碳同位素组成变化范围较小(δ13C值为－6.6‰ ～ －4.6‰),与正常地幔碳δ 13C值－5±2‰一致;而氧同位素组成变化范围较大(δ18O值为11.9‰～17.7‰ ),显著高于地幔的δ18O值5.7±1.0‰,表明碳酸岩浆在结晶过程中或之后曾与 低 温热液流体发生了同位素交换。碳酸岩墙中白云石与方解石之间的碳和氧同位素分馏均小于 0‰,处于不平衡状态,说明该碳酸岩墙中的白云石与方解石并非同成因矿物,白云石可能 为次生成因的。     

Submillimeter Scale Variation of Oxygen Isotope of Vein Quartz at the Hishikari Deposit, Japan

Abstract: The physical and chemical mechanism of gold precipitation in the typical low-sulfidation epithermal gold deposit at the Hishikari mine was quantified by submillimeter scale oxygen isotope analyses of vein quartz. In situ CO₂ laser-ablated fluorination was used to measure temporal δ¹⁸O excursions. The calculated oxygen isotopic compositions of the ore-forming fluid indicate a dynamic process of epithermal vein formation. Intermittent opening of the vein allowed introduction of metal-bearing deep fluid to the epithermal system, and associated boiling and subsequent mixing with meteoric water caused precipitation of precious metals.     

Genesis of the Mamut Porphyry Copper Deposit, Sabah, East Malaysia

Abstract: The Mamut deposit of Sabah, East Malaysia, is a porphyry type Cu‐Au deposit genetically related to a quartz monzonite (“adamellite”) porphyry stock associated with upper Miocene Mount Kinabalu plutonism. The genesis of the Mamut deposit is discussed based on petrology of the intrusives in the Mount Kinabalu area combined with ore– and alteration–petrography, fluid inclusion and sulfur isotope studies. Groundmass of the adamellite porphyry at Mamut is rich in K which suggests vapor transport of alkaline elements during the mineralizing magmatic process, while the groundmass of the post‐ore “granodiorite” porphyry at Mamut contains small amounts of normative corundum suggesting depletion in alkaline elements at the root zone of the magma column. Sub‐dendritic tremolitic amphibole rims on hornblende phenocrysts in the Mamut adamellite porphyry suggest interaction between the mineralizing magma and the exsolved fluids. Occurrences of clinopyroxene microphenocrysts and pseudomor‐phic aggregates of shredded biotite and clinopyroxene after hornblende phenocrysts in the barren intrusives imply lower water fugacity and decreasing in water fugacity, respectively. Compositional gap between the core of hornblende phenocrysts and the tremolitic amphibole rims and those in the groundmass of the Mamut adamellite porphyry suggests a decrease in pressure. Higher X_Mg (=Mg/(Mg+Fe) atomic ratio) in the tremolitic amphibole rims in the Mamut adamellite porphyry compared to those of the barren intrusions suggests high oxygen fugacity. High halogen contents of igneous hydrous minerals such as amphiboles, biotite and apatite in the Mamut adamellite porphyry suggest the existence of highly saline fluids during the intrusion and solidification of the mineralizing magma. Fluid inclusions found in quartz veinlet stockworks are characterized by abundant hypersaline polyphase inclusions associated with subordinate amounts of immiscible gaseous vapor. Both Cu and Au are dispersed in disseminated and quartz stockwork ores. Chalcopyrite and pyrrhotite as well as magnetite are the principal ore minerals in the biotitized disseminated ores. Primary assemblage of intermediate solid solution (iss) and pyrrhotite converted to the present assemblage of chalcopyrite and pyrrhotite during cooling. Subsequent to biotitization, quartz veinlet stockworks formed associated with retrograde chlorite alteration. The Cu‐Fe sul–fides associated with stockwork quartz veinlet are chalcopyrite and pyrite. Overlapping Pb and Zn and subsequent Sb mineralizations were spatially controlled by NNE‐trending fractures accompanying the phyllic and advanced argillic alteration envelope. Sulfur isotopic composition of ore sulfides are homogeneous (about +2%) throughout the mineralization stages. These are identical to those of the magmatic sulfides of Mount Kinabalu adamellitic rocks.     

青藏高原中部水蒸发过程中的氧稳定同位素变化

作为青藏高原稳定同位素水文循环的一个重部分,１９９８年夏首次在青藏高原中部的那曲和安多两地同时进行了水蒸发过程中氧稳定同位素变化观测研究,模拟和实验结果都显示出大气相对湿度对水蒸发过程中氧稳定同位素变化的显著影响,模拟结果不显示剩余水中δ＾１８Ｏ与剩余水比率呈指数关系,但实验分析结果表明,蒸发过程中剩余水中δ＾１８Ｏ与剩余水比率更接近于线性关系,这种关系可以定量地表示出来,从理论上与实验中都可以计     

中国北方石墨矿床及赋矿孔达岩系碳同位素特征及有关问题讨论

本文综合了中国北方孔达岩系和石墨矿床的碳同位素数据 10 2件 ,发现片麻岩石墨 透辉岩石墨 <大理岩石墨 <石墨大理岩方解石 <大理岩方解石 ;混合岩化岩石中石墨δ1 3C总介于有机碳和无机碳之间 ;不同地体片麻岩石墨δ1 3C极为一致 ,变化于 - 2 2 .8‰～ - 2 1.48‰ ,略低于世界有机质平均值 - 2 6± 7‰ ;大理岩的原岩碳酸盐δ1 3C高于 2‰ ,与2 330～ 2 0 6 0 Ma期间全球性δ1 3Ccarb正向漂移事件一致。地质流体是碳同位素分馏、均一化的重要因素 ,是石墨矿床的 3种主要碳源之一 ,是碳的 5种存在形式之一 ,也是碳循环的重要媒介和方式 ;导致热液矿床δ1 3C=- 5‰左右的因素较多 ,依据δ1 3Ccalcite - 5‰得出成矿物质和流体来自地幔的结论值得怀疑 ;中国北方孔达岩系形成于古元古代 ,可能为 2 30 0～ 2 0 5 0 Ma。     

松辽盆地徐家围子断陷深层天然气同位素倒转现象研究

天然气的同位素组成受源岩有机质类型、热演化程度和成藏后的次生变化等多种因素的影响, 其单体烃同位素分布特征是区分各种因素影响程度的地球化学指纹.天然气单体烃同位素通常有随碳数增加而变重的趋势, 而徐家围子深层天然气单体烃同位素倒转现象却比较普遍, 高地温和细菌氧化对于造成该区同位素倒转的可能性不大, 浅层油型气或无机气的混合作用没有充分的地质证据, 同层有机质中不同类型气的混合和盖层微渗漏造成的蒸发分馏作用可能是导致徐家围子断陷深层天然气同位素倒转的主要原因.      

Downstream composition changes of acidic volcanic waters discharged into the Banyupahit stream, Ijen caldera, Indonesia

The crater lake of Kawah Ijen volcano contains extremely low pH (<0.4) waters with high SO₄ (70000 mg/kg), Cl (21000 mg/kg), F (1500 mg/kg), Al (5000 mg/kg), Fe (2000 mg/kg) and trace metal (Cu 0.5, Zn 4, Pb 3 mg/kg) contents. These brines seep outward through the western crater rim and reappear on the other side as streamlets, which form the headwaters of the Banyupahit stream. The Banyupahit first mixes with fresh rivers and thermal springs in the Ijen caldera and then irrigates a coastal agricultural plain which is 30 km from the summit crater.We discuss the downstream composition changes affecting the Banyupahit waters by using stable isotope, chemical and mineralogical data collected from sites along the stream length. The saturation of the stream waters with respect to minerals was evaluated with SOLVEQ and WATEQ4F and compared with the geochemical observations. An aluminous mineralogy (alunogen, pickeringite, tamarugite and kalinite) develops in the upper part of the Banyupahit due to concentration of the headwaters by evaporation. Downstream attenuation of dissolved element concentrations results principally from dilution and from mineral precipitation. The stream pH changes from 0 at the source to >4 close to the mouth. The δD and δ¹⁸O values and the relative SO₄–Cl–F contents of the Banyupahit waters indicate that the tributaries are mostly meteoric. Dissolved SO₄ in the acidic stream come only from the crater lake seepages and are not involved later in microbially mediated reactions, as shown by their δ³⁴S and δ¹⁸O values. Re-equilibration of the stream SO₄ oxygen-isotope composition with H₂O from tributaries does not occur.Calcium, SiO₂, Al, Fe, K and SO₄ behave non-conservatively in the stream waters. Gypsum, silica (amorphous or poorly ordered), a basic aluminum hydroxysulfate (basaluminite?), K-jarosite and amorphous ferric hydroxide may exert a solubility control on these elements along the entire stream length, or in certain stream sections, consistent with the thermochemical model results. Downstream concentration trends and mineral saturation levels suggest that precipitation of Sr-, Pb-rich barite and celestite consume Ba, Sr and Pb, whereas dissolved Cu, Pb and Zn may adsorb onto solid particles, especially after the junctions of the acidic stream with non-acidic rivers. We calculated that significant fluxes of SO₄, F, Cl, Al, SiO₂, Ti, Mn and Cu may reach the irrigation system, possibly causing serious environmental impacts such as soil acidification and induration.