硫氧同位素示踪污染物来源在济南岩溶水中的应用   总被引：1，自引：0，他引：1  

张海林  王重  逄伟  滕跃  齐欢 《中国地质调查》2019,6(1):75-80

近年来,济南岩溶水硫酸盐浓度逐年升高,为了对硫酸盐污染区域实施有效的防治措施,保障饮用水安全,识别硫酸盐的污染来源极其重要。在系统分析研究区水文地质条件的基础上,根据实际的采样测试数据,采用硫、氧(S、O)双同位素示踪技术,分析识别了济南趵突泉泉域硫酸盐的主要污染来源,并通过IsoSource质量守恒模型,估算了硫酸盐各污染来源的贡献率。结果表明: 泉域内硫酸盐主要污染来源有大气沉降、污水和土壤; 大气沉降来源贡献率最大,均值达到53.9%; 其次是污水来源,均值为31%; 土壤来源贡献率最小,均值为15.1%。该研究为北方岩溶区地下水硫酸盐来源的定量研究提供了一种新方法,为济南趵突泉泉域硫酸盐污染防治提供了科学依据。  相似文献   

甘肃北山老金厂金矿床载金矿物特征、原位硫同位素组成及其对成矿的指示意义     

黄式庭  于晓飞  吕志成  刘家军  李永胜  杜泽忠  吕鑫  孙海瑞  杜轶伦 《吉林大学学报(地球科学版)》2020,50(5):1387-1403

老金厂金矿床是北山成矿南带最具代表性的中低温岩浆热液型金矿床之一，其规模为中型。依据脉体穿插、矿物共生组合和矿石结构构造等特征，将矿床矿化作用过程划分为石英-黄铁矿阶段（Ⅰ）、石英-含砷黄铁矿-毒砂阶段（Ⅱ）、石英-黄铁矿-多金属硫化物阶段（Ⅲ）和石英-方解石阶段（Ⅳ）。利用电子探针研究了不同成矿阶段载金矿物的元素组成及其分布规律。Ⅰ阶段：黄铁矿以粗粒自形立方体为主，粒度为0.50~1.50 mm，贫As、Au；毒砂含量极少，呈细粒他形。Ⅱ阶段：含砷黄铁矿周围常有大量毒砂产出，含砷黄铁矿多为立方体、五角十二面体，粒度为0.30~1.00 mm，富As、Au；该阶段矿化最为强烈，毒砂主要形成于此时期，多呈棱柱状、柱状、放射状集合体，显示富S亏As特征。Ⅲ阶段：多以黄铁矿-黄铜矿-闪锌矿共生组合脉的形式产出，黄铁矿多呈长条状，以富S、Cu、Zn、Au和贫Fe、As为特征。Ⅳ阶段：矿化作用极弱，毒砂、黄铁矿含量极少，为细粒他形。原位硫同位素组成显示：Ⅰ阶段黄铁矿δ³⁴S_V-CDT值为-3.8‰~-2.9‰，均值为-3.3‰；Ⅱ阶段黄铁矿和毒砂δ³⁴S_V-CDT值为-4.7‰~2.6‰，均值为-3.3‰；Ⅲ阶段黄铁矿和闪锌矿δ³⁴S_V-CDT值主要分布于-1.9‰~1.0‰之间，均值为0.1‰。此3个阶段硫同位素组成反映了成矿期硫主要来源于幔源岩浆，混入了部分地层硫。综合前人研究成果，认为成矿早期至晚期，成矿流体总体上由富S贫As向富As贫S演化。Ⅰ阶段体系处于中性稳定的环境，硫源充足；Ⅱ阶段为贫S富As的高氧逸度环境，由于大气降水对地层的淋滤渗透，混入富As流体，Au可能与As结合形成Au-As络合物，在成矿有利部位富集沉淀；Ⅲ阶段成矿元素种类丰富，体系为富S贫As的弱还原环境，Au很可能与HS^-、S^-形成络合物进入黄铁矿晶格。  相似文献   

内蒙古别鲁乌图铜多金属矿床锆石U-Pb年龄和S、Pb同位素特征及其地质意义     

郭硕  何鹏  刘洋  滕飞  胡晓佳  王文龙  杨泽黎 《现代地质》2020,(1):40-50

为了明确内蒙古别鲁乌图铜多金属矿床的成矿年龄与矿床成因,对该矿床中与成矿关系密切的流纹岩进行了锆石U-Pb年龄以及主要金属硫化物的S、Pb同位素测试。其中流纹岩的锆石206Pb/238U加权平均年龄为(271.7±1.6)Ma(MSWD=1.02),显示成矿作用发生于二叠纪。金属硫化物的S同位素分析结果显示δ34SV-CDT值分布在-0.6‰~1.0‰之间,平均为0.49‰,变化范围较窄,显示S的来源单一;Pb同位素组成比较集中,206Pb/204Pb为18.207~18.674,207Pb/204Pb为15.620~15.699,208Pb/204Pb为38.144~38.790,具有壳幔混源的特征。S、Pb同位素特征均指示成矿物质主要来源于岩浆热液。结合区域地质、矿床地质、空间分带等特征以及S、Pb同位素组成可知,别鲁乌图铜多金属矿床为VHMS型矿床,形成于二叠纪陆缘弧裂谷中。  相似文献   

南海神狐海域沉积物自生黄铁矿和石膏S同位素特征及对甲烷渗漏强度的示踪   总被引：1，自引：1，他引：0  

张美  陆红锋  管红香  刘丽华  邬黛黛  吴能友 《海洋学报(英文版)》2018,37(7):20-27

The northern slope of the South China Sea is a gas-hydrate-bearing region related to a high deposition rate of organic-rich sediments co-occurring with intense methanogenesis in subseafloor environments.Anaerobic oxidation of methane(AOM) coupled with bacterial sulfate reduction results in the precipitation of solid phase minerals in seepage sediment,including pyrite and gypsum.Abundant aggregates of pyrites and gypsums are observed between the depth of 667 and 850 cm below the seafloor(cmbsf) in the entire core sediment of HS328 from the northern South China Sea.Most pyrites are tubes consisting of framboidal cores and outer crusts.Gypsum aggregates occur as rosettes and spheroids consisting of plates.Some of them grow over pyrite,indicating that gypsum precipitation postdates pyrite formation.The sulfur isotopic values(δ~(34) S) of pyrite vary greatly(from –46.6‰ to –12.3‰ V-CDT) and increase with depth.Thus,the pyrite in the shallow sediments resulted from organoclastic sulfate reduction(OSR) and is influenced by AOM with depth.The relative high abundance and δ~(34) S values of pyrite in sediments at depths from 580 to 810 cmbsf indicate that this interval is the location of a paleo-sulfate methane transition zone(SMTZ).The sulfur isotopic composition of gypsum(from–25‰ to –20.7‰) is much lower than that of the seawater sulfate,indicating the existence of a 34 S-depletion source of sulfur species that most likely are products of the oxidation of pyrites formed in OSR.Pyrite oxidation is controlled by ambient electron acceptors such as MnO_2,iron(Ⅲ) and oxygen driven by the SMTZ location shift to great depths.The δ~(34) S values of gypsum at greater depth are lower than those of the associated pyrite,revealing downward diffusion of 34 S-depleted sulfate from the mixture of oxidation of pyrite derived by OSR and the seawater sulfate.These sulfates also lead to an increase of calcium ions from the dissolution of calcium carbonate mineral,which will be favor to the formation of gypsum.Overall,the mineralogy and sulfur isotopic composition of the pyrite and gypsum suggest variable redox conditions caused by reduced seepage intensities,and the pyrite and gypsum can be a recorder of the intensity evolution of methane seepage.  相似文献   

南海北部西沙海槽沉积物管状黄铁矿特征及其形成机理^*          下载免费PDF全文

石思思  吴朝东  梁金强  王熠哲  叶云涛  方允鑫  马健  翟俪娜 《古地理学报》2020,22(1):175-192

南海北部西沙海槽S1站位的岩心柱沉积物中广泛发育自生矿物黄铁矿,其形态以管状为主,且具有内部中空的圈层结构。使用扫描电镜、电子探针、LA-ICP-MS、SIMS等测试方法研究了管状黄铁矿的形态及圈层结构,结果显示: (1)管状黄铁矿发育内部中空的圈层结构,其中内圈层(I_py)由莓球状黄铁矿呈五角十二面体紧密堆积组成,外圈层(O_py)由晶形较好晶粒较大的八面体黄铁矿组成,并混有沉积碎屑及钙质生物壳体;(2)内圈层和外圈层分别呈现出贫S富Fe和富S贫Fe的特征,其成因是甲烷渗漏造成的局部还原环境使得As进入黄铁矿中导致晶格空缺或被扭曲,从而促进Ni、Co、Cu、Zn、Pb等微量元素的掺入;(3)内圈层、外圈层发生了明显的硫同位素分馏现象,内圈层中 δ³⁴S 平均为-37.8‰,外圈层中 δ³⁴S 平均为-29.3‰。研究认为,管状黄铁矿作为曾经甲烷渗漏的通道,其生长机制可分为3个阶段: (1)气水通道形成阶段: 向上运移的甲烷流体在沉积物孔隙中逐渐形成气水通道;(2)外圈层形成阶段: 当向上运移的甲烷与硫酸盐发生甲烷厌氧氧化时,逐渐形成晶体较大、晶形较好的八面体黄铁矿外圈层;(3)内圈层形成阶段: 随着甲烷浓度逐渐降低,在气水通道中的微生物作用下,剩余甲烷与向下运移的硫酸盐继续反应形成莓球状黄铁矿内圈层。因此,南海北部的泥岩中大量发育的管状黄铁矿常常与地层中甲烷水合物的存在有关。  相似文献   

Origin of natural sulfur-metal chimney in the Tangyin hydrothermal field,Okinawa Trough: constraints from rare earth element and sulfur isotopic compositions     

《China Geology》2018,1(2):225-235

For the first time, we present the rare earth element (REE) and sulfur isotopic composition of hydrothermal precipitates recovered from the Tangyin hydrothermal field (THF), Okinawa Trough at a water depth of 1206 m. The natural sulfur samples exhibit the lowest ΣREE concentrations (ΣREE= 0.65×10^–6–4.580×10^–6) followed by metal sulfides (ΣREE=1.71×10^–6–11.63×10^–6). By contrast, the natural sulfur-sediment samples have maximum ΣREE concentrations (ΣREE=11.54×10^–6–33.06×10^–6), significantly lower than those of the volcanic and sediment samples. Nevertheless, the δEu, δCe, (La/Yb)_N, La/Sm, (Gd/Yb)_N and normalized patterns of the natural sulfur and metal sulfide show the most similarity to the sediment. Most hydrothermal precipitate samples are characterized by enrichments of LREE (LREE/HREE=10.09–24.53) and slightly negative Eu anomalies or no anomaly (δEu=0.48–0.99), which are different from the hydrothermal fluid from sediment-free mid-oceanic ridges and back-arc basins, but identical to the sulfides from the Jade hydrothermal field. The lower temperature and more oxidizing conditions produced by the mixing between seawater and hydrothermal fluids further attenuate the leaching ability of hydrothermal fluid, inducing lower REE concentrations for natural sulfur compared with metal sulfide; meanwhile, the negative Eu anomaly is also weakened or almost absent. The sulfur isotopic compositions of the natural sulfur (δ³⁴S=3.20‰–5.01‰, mean 4.23‰) and metal sulfide samples (δ³⁴S=0.82‰–0.89‰, mean 0.85‰) reveal that the sulfur of the chimney is sourced from magmatic degassing.  相似文献   

The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)     

V.V. Ryabov  O.N. Simonov  S.G. Snisar  A.A. Borovikov 《Russian Geology and Geophysics》2018,59(8):945-961

The source of sulfur in giant Norilsk-type sulfide deposits is discussed. A review of the state of the problem and a critical analysis of existing hypotheses are made. The distribution of δ³⁴S in sulfides of ore occurrences and small and large deposits and in normal sedimentary, metamorphogenic, and hypogene sulfates is considered. A large number of new δ³⁴S data for sulfides and sulfates in various deposits, volcanic and terrigenous rocks, coals, graphites, and metasomatites are presented. The main attention is focused on the objects of the Norilsk and Kureika ore districts. The δ³⁴S value varies from -14 to + 22.5‰ in sulfides of rocks and ores and from 15.3 to 33‰ in anhydrites. In sulfide-sulfate intergrowths and assemblages, δ³⁴S is within 4.2-14.6‰ in sulfides and within 15.3-21.3‰ in anhydrites. The most isotopically heavy sulfur was found in pyrrhotite veins in basalts (δ³⁴S = 21.6‰), in sulfate veins cutting dolomites (δ³⁴S = 33‰), and in subsidence caldera sulfates in basalts (δ³⁴S = 23.2-25.2‰). Sulfide ores of the Tsentral’naya Shilki intrusion have a heavy sulfur isotope composition (δ³⁴S = + 17.7‰ (n = 15)). Thermobarogeochemical studies of anhydrites have revealed inclusions of different types with homogenization temperatures ranging from 685 °C to 80 °C. Metamorphogenic and hypogene anhydrites are associated with a carbonaceous substance, and hypogene anhydrites have inclusions of chloride-containing salt melts. We assume that sulfur in the trap sulfide deposits was introduced with sulfates of sedimentary rocks (δ³⁴S = 22-24‰). No assimilation of sulfates by basaltic melt took place. The sedimentary anhydrites were “steamed” by hydrocarbons, which led to sulfate reduction and δ³⁴S fractionation. As a result, isotopically light sulfur accumulated in sulfides and hydrogen sulfide, isotopically heavy sulfur was removed by aqueous calcium sulfate solution, and “residual” metamorphogenic anhydrite acquired a lighter sulfur isotope composition as compared with the sedimentary one. The wide variations in δ³⁴S in sulfides and sulfates are due to changes in the physicochemical parameters of the ore-forming system (first of all, temperature and P_ch4) during the sulfate reduction. The regional hydrocarbon resources were sufficient for large-scale ore formation.  相似文献   

滇东南都龙Sn-Zn多金属矿床交生硫化物微区主量元素、硫同位素特征及成因研究     

许赛华  任涛  白鑫  叶勤富  韩彬 《矿床地质》2022,41(4):741-750

都龙Sn-Zn多金属矿床位于滇东南老君山锡锌钨多金属成矿区南部,是中国3大锡石硫化物矿床之一。该矿床发育闪锌矿-黄铜矿-磁黄铁矿密切共生结构,即硫化物交生结构。文章利用电子探针和LA-MC-ICP-MS对具有交生结构的闪锌矿-黄铜矿-磁黄铁矿和毒砂进行了微区主量元素和硫同位素测试,以期明确其成因及硫的来源。主量元素测试结果显示,闪锌矿中的w(Zn)为52.23%~57.22%,w(S)为33.06%~36.10%,w(Fe)为9.92%~12.24%,w(Cu)为0.11%~0.30%;黄铜矿中的w(Cu)为33.95%~35.08%,w(S)为33.49%~35.27%,w(Fe)为30.74%~31.41%,w(Zn)为0.04%~1.50%;磁黄铁矿中的w(Fe)为49.30%~51.94%,w(S)为38.36%~39.69%,w(Zn)为9.35%~11.01%,w(Cu)为0.05%~0.15%。磁黄铁矿和黄铜矿包裹体边部和核部成分均一,且投影点全部落在固溶体出溶区域,说明都龙矿床交生闪锌矿-黄铜矿-磁黄铁矿是固溶体分离成因。原位S同位素分析结果显示,闪锌矿的δ³⁴S为0.9‰~3.2‰,磁黄铁矿的δ³⁴S为0.6‰~2.1‰,毒砂的δ³⁴S为2.9‰~4.2‰,黄铜矿的δ³⁴S为0.6‰~2.8‰,均显示为岩浆来源特征。主量元素温度计估算的闪锌矿-黄铜矿的形成温度介于285~394℃,指示该矿床主要硫化物形成于中高温阶段。  相似文献   

陕西旬阳地区小河金矿硫铅同位素组成及地质意义     

孟五一  刘家军  魏立勇  张振  吴欢欢  范堡程  潘元  李国英  贾彬 《现代地质》2021,35(6):1587-1596

小河金矿是近年来在南秦岭中带发现的中型金矿床,矿石类型为微细浸染型,矿床受地层和构造双重控制。在野外工作基础上,根据矿物组合及穿插关系划分了4个成矿阶段:Ⅰ,成矿早期少硫化物石英脉成矿阶段;Ⅱ,石英脉、黄铁矿、毒砂成矿主阶段;Ⅲ,石英脉-多金属硫化物成矿主阶段;Ⅳ,方解石、石英脉成矿晚阶段。其中Ⅱ、Ⅲ阶段是主要金矿化阶段。不同阶段样品的原位硫同位素结果显示:成矿早阶段石英脉期的黄铁矿δ³⁴S值为20.80‰~25.77‰,均值为23.59‰;主成矿期II阶段中黄铁矿、毒砂δ³⁴S值为15.46‰~19.12‰,均值为17.5‰;主成矿期Ⅲ阶段中方铅矿、闪锌矿δ³⁴S值为11.35‰~16.78‰,均值为13.88‰。硫同位素特征指示硫以沉积硫为主,成矿过程可能存在低δ³⁴S值热液的持续加入。金属硫化物Pb同位素测试结果显示²⁰⁶Pb/²⁰⁴Pb为17.882 1~18.367 4,²⁰⁷Pb/²⁰⁴Pb为15.614 0~15.674 1,²⁰⁸Pb/²⁰⁴Pb为38.016 3~38.934 2,指示小河金矿铅主要源于地壳,同时伴随幔源铅的混入。综合矿床地质特征及硫、铅同位素地球化学特征,认为小河金矿成矿过程可能存在流体混合作用。  相似文献   

南秦岭柞水—山阳矿集区夏家店金矿床黄铁矿微量元素和氢、氧、硫同位素对矿床成因的制约     

丁坤  王瑞廷  刘凯  王智慧  申喜茂 《现代地质》2021,35(6):1622-1632

为了研究柞水—山阳矿集区夏家店金矿床成因,采用LA-ICP-MS和LA-MC-ICP-MS技术分析夏家店金矿床矿体及围岩样品中黄铁矿原位微量元素及氢、氧、硫同位素组成特征。结果表明,该矿床黄铁矿的Co/Ni 比值为0.11~0.76,说明其与沉积作用有关。矿石中黄铁矿的δ³⁴S值(-9.40‰~7.16‰)与围岩碳质板岩的δ³⁴S值(-8.84‰~10.64‰)接近,黄铁矿的δ³⁴S均值(2.47‰)基本落在岩浆硫的范围内,指示矿石硫可能由地层硫和岩浆硫混合而成。氢、氧同位素测试结果表明,夏家店矿床成矿流体可能主要来自岩浆水,成矿后期有大气降水的加入。综合矿床地质特征、成矿温度、金赋存状态等特征和黄铁矿微量元素、硫同位素组成可知,夏家店金矿床属于卡林型金矿,其成矿流体主要来自岩浆水,成矿后期有大气降水加入;其成矿物质是由深部岩浆与地层混合而成。  相似文献