陕西略阳煎茶岭镍矿床成矿及矿石变质过程的地球化学研究     

Zhang Benren Chen Dexing Hu Yikeng 《地球科学》1986,(4)

矿床中存在着岩浆离熔成因的磁黄铁矿-镍黄铁矿矿石和热液改造成因的黄铁矿-针镍矿-辉镍矿矿石。研究证明现在矿石中存在的硫化物均为较低温度条件下的变质产物,并且矿物组合的更替不仅同温度变化有关,同时还受体系中氧逸度和硫离子活度的控制。矿物组合的地球化学分析表明,现有Fe-Ni-S体系低温（<300℃）相平衡图解之间存在着矛盾的原因可能是忽略了氧化-还原条件的影响。  相似文献   

Sulfides in petroleum     

J.D. Payzant  D.S. Montgomery  O.P. Strausz   《Organic Geochemistry》1986,9(6)

The homologous series of terpenoid sulfides previously reported to be present in Athabasca bitumen have been detected in a variety of petroleums from the Western Hemisphere. All 22 samples examined, ranging in age from Devonoan to Cretaceous, contained the terpenoid sulfides. A method is described for the isolation of sulfides from petroleums based on the selective oxidation of sulfides to more polar sulfoxides which are easily removed from the mixture and their subsequent reduction to sulfides. The sulfide content in the petroleum maltenes examined ranged from 0.3 to 16.1% w/w. In addition to the bicyclic and tetracyclic terpenoid sulfides a new series of tricyclic terpenoid sulfides has been identified, and the details of the isoprenoid side chain have been elucidated for all three homologous series. The distributions by carbon number of the bicyclic and tetracyclic homologous series of terpenoid sulfides show pronounced variations which are attributed to thermal maturity and degree of water washing of the petroleum, thus the ability to identify terpenoid sulfides should provide a useful tool for oil-oil and oil-source rock correlation studies. The bicyclic and tricyclic terpenoid sulfides have the same carbon framework as the carotenoids which suggest that these sulfides were accessory pigments in photosynthesis.  相似文献   

Factors Controlling Sulfide Geochemistry in Sub-tropical Estuarine and Bay Sediments     

John W. Morse  Heather Thomson  David W. Finneran 《Aquatic Geochemistry》2007,13(2):143-156

The primary factors that control the concentration of total reduced (inorganic) sulfide in coastal sediments are believed to be the availability of reactive iron, dissolved sulfate and metabolizable organic carbon. We selected nine sites in shallow (<3 m), close to sub-tropical, estuaries and bays along the central Texas coast that represented a range in sediment grain size (a proxy for reactive iron), salinity (a proxy for dissolved sulfate), and total organic carbon (a proxy for metabolizable organic carbon). Based on these parameters a prediction was made of which factor was likely to control total reduced sulfide at each site and what the relative total reduced sulfide concentration was likely to be. To test the prediction, the sediments were analyzed for total reduced sulfide, acid volatile sulfide, and citrate dithionate-extractable, HCl-extractable and total Fe in the solid phase. Using solid-state gold–mercury amalgam microelectrodes and voltammetry, we determined pore water depth profiles of Fe(II) and ΣH₂S and presence or absence of FeS_(aq). At five of the nine sites the calculated degree of sufildization of citrate dithionite-reactive-iron was close to or greater than 1 indicating that rapidly reactive iron was probably the limiting factor for iron sulfide mineral formation. At one site (salinity = 0.9) dissolved Fe(II) was high, ΣH₂S was undetectable and the total reduced sulfide concentration was low indicating sulfate limitation. At the last three sites a low degree of sulfidization and modest total reduced (inorganic) sulfide concentrations appeared to be the result of a limited supply of metabolizable organic carbon. Fe(II)–S(-II) clusters (FeS_(aq)) were undetectable in 10 out of 12 bay sediment profiles where ΣH₂S was close to or below detection limits, but was observed in all other porewater profiles. Acid volatile sulfide, but not total reduced sulfide, was well correlated with total organic carbon and ranged from being undetectable in some cores to representing a major portion of total reduced sulfide in other cores. Although predicted controls on total reduced sulfide were good for very low salinity water or sandy sediments, they were only right about half the time for the other sediments. The likely reasons for the wrong predictions are the poor correlation of total organic carbon with grain size and differing fractions of metabolizable organic carbon in different sedimentary environments. Differences in sediment accumulation rates may also play a role, but these are difficult to determine in this region where hurricanes often resuspend and move sediments. This study demonstrates the need to examine more complex and often difficult to determine parameters in anoxic “normal marine” sediments if we are to understand what controls the concentration and distribution of sulfides.  相似文献   

新疆霍什布拉克铅锌矿床微量元素地球化学     

李志丹  薛春纪  董新丰  王思程  张岩 《岩石矿物学杂志》2014,33(3):540-550

霍什布拉克铅锌矿床是新疆西南天山地区晚古生代碳酸盐岩容矿的重要矿床。本文采用高精度电感耦合等离子质谱(ICP-MS)对主要矿石矿物(黄铁矿、方铅矿、闪锌矿)和热液脉石矿物方解石进行了微量元素地球化学研究。研究表明,黄铁矿、方铅矿、闪锌矿、方解石具有较为相似的稀土元素特征,Eu正异常明显,弱负或弱正Ce异常指示成矿流体最初由相对氧化的条件演化为还原条件。与霍什布拉克岩体、容矿围岩的稀土元素组成进行对比后发现,硫化物及热液方解石稀土元素配分曲线部分与重结晶泥晶灰岩重合,结合前人同位素地球化学研究,认为容矿坦盖塔尔组碳酸盐岩为成矿提供了必要的成矿物质及成矿流体组分。Ga/In值显示闪锌矿为低温成矿;硫化物明显富集LREE,Hf/Sm、Nb/La和Th/La值小于1,显示铅锌成矿过程中成矿流体主体以富Cl为特征;Y/Ho、Zr/Hf和Nb/Ta值变化范围相对较小,表明成矿期流体性质相对较为稳定,基本未混入外来流体。  相似文献   

Sulfide‐bearing palaeokarst deposits at Lune River Quarry,Ida Bay,Tasmania     

R. A. L. Osborne  I. B. Cooper 《Australian Journal of Earth Sciences》2013,60(3):409-416

The Lune River Quarry at Ida Bay, Tasmania exposes numerous palaeokarst features developed in the Ordovician Gordon Limestone. These palaeokarst features contain carbonate and siliciclastic deposits probably representing Late Devonian to early Late Carboniferous and Late Carboniferous karstification and sedimentation. Five facies of palaeokarst deposits are recognised, namely megabreccia, graded‐bedded carbonate, laminated sandstone/siltstone, diamictite/quartz‐lithic sandstone and coarse crystalline calcite. Pyrite, dolomite and sphalerite were emplaced in the palaeokarst deposits after the Carboniferous. These deposits are probably associated with a phase of hydrothermal cave development in Exit Cave, which adjoins the quarry. Pyrite weathering accounts for the abundance of gypsum speleothems and cave breakdown in Exit Cave.  相似文献   

硫化物吸附金属离子的实验研究──Ⅱ．温度与介质条件的影响     

吴大清  彭金莲  陈国玺 《地球化学》1996,(3)

合成ＰｂＳ和ＺｎＳ对Ａｇ２＋、Ｃｕ２＋、Ｃｄ２＋、Ｆｅ２＋、Ｍｎ２＋、Ｍｇ２＋、Ｓｂ２＋和Ｂｉ３＋等离子吸附量与温度关系的实验研究表明，其遵从Ｋｅｌｖｉｎ公式：在Ａ类吸附，即抗衡离子交换型吸附中，温度上升，其吸附量升降由反应热决定，本实验中Ａ类吸附多为上升型；而大部分Ｂ和Ｃ类吸附，即朗谬尔型及反朗谬尔型的吸附量则随温度上升呈指数下降。例外的仅有ＰｂＳ对Ｂｉ３＋离子的吸附，其吸附量随温度上升有微弱的上升。这可能与Ｂｉ３＋离子和吸附剂ＰｂＳ之间共晶反应和铅的铋硫盐的形成有关。Ａ类吸附的吸附量受介质条件变化影响很少。但对Ｂ和Ｃ类吸附，吸附量受ｐＨ和离子强度变化影响取决于三个因素：①吸附剂ＰｂＳ、ＺｎＳ表面电荷特性；②溶液介质条件变化时吸附离子在溶液中离子态的分布与变化；③被吸附离子在吸附剂中扩散和形成化合物或共晶的能力。因此，当ｐＨ增加时，Ｐｂｓ和ＺｎＳ对金属离子吸附量的变化表现出多样性：增加的有ＰｂＳ对Ｆｅ２＋离子的吸附；下降的有ＰｂＳ对Ｓｂ３＋离子的吸附和ＺｎＳ对Ｆｅ２＋、Ｍｎ２＋离子的吸附；不变的有ＰｂＳ对Ｂｉ３＋、Ｚｎ２＋离子的吸附和ＺｎＳ对Ｍｇ２＋离子的吸附。当溶液中离子强度增加时，由于溶液中自由态离子  相似文献   

Equilibrium thallium isotope fractionation and its constraint on Earth’s late veneer     

Tong Fang  Yun Liu 《Acta Geochimica》2019,(4):459-471

Equilibrium isotope fractionation of thallium(Tl) includes the traditional mass-dependent isotope fractionation effect and the nuclear volume effect(NVE). The NVE dominates the overall isotope fractionation, especially at high temperatures. Heavy Tl isotopes tend to be enriched in oxidized Tl^3+-bearing species. Our NVE fractionation results of oxidizing Tl^+ to Tl^3+ can explain the positive enrichments observed in ferromanganese sediments. Experimental results indicate that there could be0.2–0.3 e-unit fractionation between sulfides and silicates at 1650 ℃. It is consistent with our calculation results,which are in the range of 0.17–0.38 e-unit. Importantly,Tl’s concentration in the bulk silicate Earth(BSE) can be used to constrain the amount of materials delivered to Earth during the late veneer accretion stage. Because the Tl concentration in BSE is very low and its Tl isotope composition is similar with that of chondrites, suggesting either no Tl isotope fractionation occurred during numerous evaporation events, or the Tl in current BSE was totally delivered by late veneer. If it is the latter, the Tl-contentbased estimation could challenge the magnitude of late veneer which had been constrained by the amount of highly siderophile elements in BSE. Our results show that the lateaccreted mass is at least five-times larger than the previously suggested magnitude, i.e., 0.5 wt% of current Earth’s mass. The slightly lighter 205 Tl composition of BSE relative to chondrites is probable a sign of occurrence of Tlbearing sulfides, which probably were removed from the mantle in the last accretion stage of the Earth.  相似文献   

Mineralogical characteristics of polymetallic sulfides from the Deyin-1 hydrothermal field near 15°S,southern Mid-Atlantic Ridge   总被引：1，自引：0，他引：1  

王淑杰  李怀明  翟世奎  于增慧  邵宗泽  蔡宗伟 《海洋学报(英文版)》2017,36(2):22-34

A seafloor hydrothermal field, named Deyin-1 later, near 15°S southern Mid-Atlantic Ridge(SMAR) was newly found during the 22 nd cruise carried out by the China Ocean Mineral Resources Research Development Association(COMRA). Sulfide samples were collected at three stations from the hydrothermal field during the26 th cruise in 2012. In this paper, mineralogical characteristics of the sulfides were analyzed with optical microscope, X-ray diffractometer, scanning electron microscope and electron microprobe to study the crystallization sequence of minerals and the process of hydrothermal mineralization. According to the difference of the ore-forming metal elements, the sulfide samples can be divided into three types:(1) the Ferich sulfide, which contains mainly pyrite and chalcopyrite;(2) the Fe-Cu-rich sulfide consisting predominantly of pyrite, chalcopyrite and isocubanite, with lesser amount of sphalerite, marmatite and pyrrhotine; and(3) the Fe-Zn-rich sulfide dominated by pyrite, sphalerite and marmatite, with variable amounts of chalcopyrite, isocubanite, pyrrhotine, marcasite, galena and gratonite. Mineral precipitations in these sulfides are in the sequence of chalcopyrite(isocubanite and possible coarse pyrite), fine pyrite,sphalerite(marmatite), galena, gratonite and then the minerals out of the dissolution. Two morphologically distinct generations(Py-I and Py-II) of pyrite are identified in each of the samples; inclusions of marmatite tend to exist in the coarse pyrite crystals(Py-I). Sphalerite in the Fe-Zn-rich sulfide is characterized by a"chalcopyrite disease" phenomenon. Mineral paragenetic relationships and a wide range of chemical compositions suggest that the environment of hydrothermal mineralization was largely changing. By comparison, the Fe-rich sulfide was formed in a relatively stable environment with a high temperature, but the conditions for the formation of the Fe-Cu-rich sulfide were variable. The Fe-Zn-rich sulfide was precipitated during the hydrothermal venting at relatively low temperature.  相似文献   

Re-Suspension Technique for Improving Organic Rich Sediment-Water Quality in a Shallow Sea Area     

Masaharu Fukue  Koji Uehara  Yoshio Sato  Catherine Mulligan 《Marine Georesources & Geotechnology》2013,31(3):222-233

The re-suspension method consists of (1) dispersion of the sediment by air-water jets, (2) pumping of the suspension (small particles and organic matter), (3) settlement in a tank, (4) filtration and (5) disposal of solids (followed by incineration in this case). The pilot test was performed to clean up an area of 3000 m². The dispersed depth of the bottom was approximately 50 cm. The time spent for the work was two weeks. The amount of re-suspended solid removed from the bottom was about 8 tonnes in dry mass. Since the solids contain high concentrations of chemical oxygen demand (COD), total phosphorous (T-P), total nitrogen (T-N) and sulfides, the remaining sediment was considerably improved. Quantitative analyses showed that the full-scale implementation would enable the removal of about 10% of the re-suspended solids, and reduce COD by 95%, T-P by 50%, T-N by 100% and sulfide by 75% for re-deposited sediments in comparison to the original sediments.  相似文献   

Shallow Drilling of Seafloor Hydrothermal Systems Using the BGS Rockdrill: Conical Seamount (New Ireland Fore-Arc) and PACMANUS (Eastern Manus Basin), Papua New Guinea     

Sven Petersen  Peter M. Herzig  Thomas Kuhn  Leander Franz  Mark D. Hannington  Thomas Monecke 《Marine Georesources & Geotechnology》2013,31(3):175-193

ABSTRACT

From September to October 2002, shallow drilling, using the submersible (5 m) Rockdrill of the British Geological Survey and the German R/V Sonne revealed critical information on the subsurface nature of two distinct hydrothermal systems in the New Ireland fore-arc and the Manus Basin of Papua New Guinea. Drilling at Conical Seamount significantly extends the known surface extent of the previously discovered vein-style gold mineralization (up to 230 g/t Au) at this site. Drilling the conventional PACMANUS volcanic-hosted massive sulfide deposit recovered complexly textured massive sulfide with spectacular concentrations of gold in several core sections including 0.5 m @ 28 g/t Au, 0.35 m @ 30 g/t Au, and 0.20 m @ 57 g/t Au. Shallow drilling is a fast and cost efficient method that bridges the gap between surface sampling and deep (ODP) drilling and will become a standard practice in the future study of seafloor hydrothermal systems and massive sulfide deposits.  相似文献