新元古代—寒武纪硫同位素异常事件(Yudomski事件)的起源与结束          下载免费PDF全文

张智礼  孟凡巍  倪培  李慧莉  卓勤功 《盐湖研究》2020,28(4):22-28

新元古代晚期—寒武纪早期是地球历史演化的关键时期,整个生物圈、大气圈和水圈在此期间都发生了巨大的变化,海水成分在其间也发生了明显的变化。而石盐流体包裹体恰恰记录了该时段海水主要离子成分的转变:海水成分从新元古代晚期的“文石海”,快速转化为寒武纪的“方解石海”；同时海水中的碳、锶、硫同位素都发生了剧烈的改变,其中海水硫酸根的硫同位素从新元古代冰期前的20‰左右,迅速升高到新元古代冰期后的35‰左右,甚至可以到45‰,海相蒸发岩沉积中的硫酸盐沉积(主要是石膏、硬石膏)则直接记录了当时海水中硫酸根的硫同位素变化。现有研究表明,新元古代晚期——寒武纪时期的海相蒸发岩沉积记录了当时海洋中存在着地质历史时期最大的硫同位素异常,即“Yudomski事件”。塔里木盆地的寒武纪早期、中期蒸发岩记录了“Yudomski事件”的硫同位素异常高值(35‰左右,甚至更高),表明这一起源于新元古代晚期的同位素异常事件持续到了寒武纪的早期和中期；塔里木盆地奥陶纪早期的蒸发岩、鄂尔多斯盆地奥陶纪中期蒸发岩和美国Williston盆地奥陶纪晚期地层的蒸发岩的硫同位素数据相似,都在+25‰左右则记录了较低的海洋硫同位素值,表明起源于新元古代冰期之后的“Yudomski事件”的硫同位素异常,持续到了寒武纪的中期,而结束于寒武纪的晚期。  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   

Highly Oxidized Magma and Fluid Evolution of Miocene Qulong Giant Porphyry Cu‐Mo Deposit,Southern Tibet,China     

Bo XIAO  Kezhang QIN  Guangming LI  Jinxiang LI  Daixiang XIA  Lei CHEN  Junxing ZHAO 《Resource Geology》2012,62(1):4-18

The Miocene Qulong porphyry Cu‐Mo deposit, which is located at the Gangdese orogenic belt of Southern Tibet, is the largest porphyry‐type deposit in China, with confirmed Cu ～10 Mt and Mo ～0.5 Mt. It is spatially and temporally associated with multiphase granitic intrusions, which is accompanied by large‐scale hydrothermal alteration and mineralization zones, including abundant hydrothermal anhydrite. In addition to hydrothermal anhydrite, magmatic anhydrite is present as inclusions in plagioclase, interstitial minerals between plagioclase and quartz, and phenocrysts in unaltered granodiorite porphyry, usually in association with clusters of sulfur‐rich apatite in the Qulong deposit. These observations indicate that the Qulong magma‐hydrothermal system was highly oxidized and sulfur‐rich. Three main types of fluid inclusions are observed in the quartz phenocrysts and veins in the porphyry: (i) liquid‐rich; (ii) polyphase high‐salinity; and (iii) vapor‐rich inclusions. Homogenization temperatures and salinities of all type inclusions decrease from the quartz phenocrysts in the porphyry to hydrothermal veins (A, B, D veins). Microthermometric study suggests copper‐bearing sulfides precipitated at about 320–400°C in A and B veins. Fluid boiling is assumed for the early stage of mineralization, and these fluids may have been trapped at about 35–60 Mpa at 460–510°C and 28–42 Mpa at 400–450°C, corresponding to trapping depths of 1.4–2.4 km and 1.1–1.7 km, respectively.  相似文献   

辽宁砖庙矿区硼矿床硬石膏的发现及成因讨论   总被引：1，自引：0，他引：1  

黄作良  莫珉 《现代地质》1996,10(3):350-355

在对辽宁砖庙矿区硼矿床的矿物学研究中发现了硬石膏。该矿物产于硼矿体中，与遂安石、菱镁矿、镁橄榄石、袁复礼石、硼铝镁石等共生。通过矿物学研究和稀土元素、硫同位素的分析表明，由于硬石膏是蒸发沉积变质成因的，所以硼矿床也应是蒸发沉积变质成因的  相似文献   

常温和压力0.1～1300 MPa下硬石膏的拉曼光谱研究   总被引：1，自引：0，他引：1  

杨玉萍  郑海飞 《矿物学报》2005,25(3):299-302

利用立方氧化锆压腔装置测量了高压下硬石膏中硫酸根离子内部S-O键的四个振动（对称伸缩振动、弯曲振动、反对称伸缩振动和变形弯曲振动）的拉曼位移，研究结果表明：在25℃和0．1～1300MPa压力范围内硬石膏未发生相变，所观察到的硬石膏各个拉曼峰的位移值随压力的增加而线性增加，它们与压力之间的关系可分别表达为：υ1018=0．0053p＋1016.8，υ417=0．0013p＋416．82，υ498=0．0044P＋499．25，υ1129=0．0052p＋1128．5，υ1160=0．0067p＋1159．5，υ608=0．0028p＋608．76，υ627=0．0036p＋627．01，υ675=0．0039p＋675．32，且伸缩振动受压力的影响比弯曲振动大。其1018cm^-1峰强度大，是石英464cm^-1峰的6倍，因此硬石膏也是宝石压腔良好的压力标定物质。  相似文献   

Solubility of Anhydrite, CaSO4, in NaCl-H2O Solutions at High Pressures and Temperatures: Applications to Fluid-Rock Interaction   总被引：1，自引：0，他引：1  

NEWTON  ROBERT C.; MANNING  CRAIG E. 《Journal of Petrology》2005,46(4):701-716

Anhydrite solubility in H₂O–NaCl solutions was measuredat 6–14 kbar, 600–800°C and NaCl mole fractions(X_NaCl) of 0–0·3 in piston–cylinder apparatus.Solubilities were determined by weight changes of natural anhydritein perforated Pt envelopes confined with fluid in larger Ptcapsules. In initially pure H₂O at 10 kbar and 800°C, CaSO₄concentration is low (0·03 molal), though much largerthan at the same temperature and 1 kbar. Hematite-buffered experimentsshowed slightly lower solubilities than unbuffered runs. CaSO₄solubility increases enormously with NaCl activity: at 800°Cand 10 kbar and X_NaCl of 0·3, CaSO₄ molality is 200 timeshigher than with pure H₂O. Whereas CaSO₄ solubility in pureH₂O decreases with rising T at low T and P, the high-P resultsshow that anhydrite solubility increases with T at constantP at all X_NaCl investigated. The effects of salinity and temperatureare so great at 10 kbar that critical mixing between sulfate-richhydrosaline melts and aqueous salt solutions is probable at900°C at X_NaCl 0·3. Recent experimental evidencethat volatile-laden magmas crystallizing in the deep crust mayevolve concentrated salt solutions could, in light of the presentwork, have important implications regarding such diverse processesas Mount Pinatubo-type S-rich volcanism, high-f O₂ regionalmetamorphism, and emplacement of porphyry Cu–Mo ore bodies,where anhydrite–hematite alteration and fluid inclusionsreveal the action of very oxidized saline solutions rich insulfur. KEY WORDS: anhydrite; sulfur; solubility; metamorphic brines; granulites  相似文献   

Gypsum–anhydrite transformations in Messinian evaporites of central Tuscany (Italy)     

G. Testa  S. Lugli 《Sedimentary Geology》2000,130(3-4):249-268

The Messinian succession of Tuscany (central Italy) contains three evaporitic units. Among the several exposed evaporitic lithofacies, only selenitic gypsum precipitated directly from evaporating brines. All the other facies, nodular microcrystalline gypsum, gypsarenites and gypsum laminites, despite their macroscopic differences, display the same petrographic textures, indicating that they are the product of dehydration of gypsum to give anhydrite which has been successively rehydrated to secondary gypsum. These secondary facies show an entire array of textures ranging from cloudy ameboid (xenotopic) with anhydrite relics, to idiotopic without anhydrite relics, that are here interpreted as a sequence of progressive stages of rehydration. The presence of completely hydrated petrofacies at the core of nodules which display a less hydrated rim suggests that these rocks have undergone at least two cycles of a dehydration–rehydration process. This interpretation is supported by the presence of satin spar veins that are replaced by microcrystalline gypsum. Satin spar itself is considered to be a by-product of anhydrite hydration. The first dehydration–rehydration event affected the entire gypsum deposit, producing a completely hydrated (idiotopic) facies together with satin spar veins; the second affected only veins, fractures and the rims of nodules, turning the first generation of satin spar and idiotopic gypsum into cloudy ameboid gypsum. Sedimentary structures typical of sabkha environments indicate for the youngest formation that the first dehydration and rehydration process occurred syndepositionally. The preservation of primary gypsum facies only at sites with condensed sections, indicate for the oldest two formations that the first dehydration event occurred upon burial. This event has been estimated to have occurred in the earliest Pliocene. After the Early Pliocene, dehydration was favored even at shallow depths, due to an increased heat flow related with the emplacement of local crustal magmatic bodies. Rehydration possibly occurred when these formations were uplifted and exposed to ground and/or meteoric water. The Volterra Basin has undergone alternating subsidence and uplift events, that can account for two dehydration–rehydration processes at least, also driven by alternating circulation, in the tectonic fractures, of fresh and salty water, the latter derived from dissolution of Messinian halite.  相似文献   

Implication of Apatite and Anhydrite for Formation of an Iron‐Oxide‐Apatite (IOA) Rare Earth Element Prospect,Benjamin River,Canada          下载免费PDF全文

Mihoko Hoshino  Yasushi Watanabe  Yoshiaki Kon 《Resource Geology》2017,67(4):361-383

The Benjamin River apatite prospect in northern New Brunswick, Canada, is hosted by the Late Silurian Dickie Brook plutonic complex, which is made up of intrusive units represented by monzogranite, diorite and gabbro. The IOA ores, composed mainly of apatite, augite, and magnetite at Benjamin River form pegmatitic pods and lenses in the host igneous rocks, the largest of which is 100 m long and 10–20 m wide in the diorite and gabbro units. In this study, 28 IOA ore and rock samples were collected from the diorite and gabbro units. Mineralogical observations show that the apatite–augite–magnetite ores are variable in the amounts of apatite, augite, and magnetite and are associated with minor amounts of epidote‐group minerals (allanite, REE‐rich epidote and epidte) and trace amounts of albite, titanite, ilmenite, titanomagnetite, pyrite, chlorite, calcite, and quartz. Apatite and augite grains contain small anhydrite inclusions. This suggests that the magma that crystallized apatite and augite had high oxygen fugacity. In back scattered electron (BSE) images, apatite grains in the ores have two zones of different appearance: (i) primary REE‐rich zone; and (ii) porous REE‐poor zone. The porous REE‐poor zones mainly appear in rims and/or inside of the apatite grains, in addition to the presence of apatite grains which totally consist of a porous REE‐poor apatite. This porous REE‐poor apatite is characterized by low REE (<0.84 wt%), Si (<0.28 wt%), and Cl (<0.17 wt%) contents. Epidote‐group minerals mainly occur in grain boundary between the porous REE‐poor apatite and augite. These indicate that REE leached from primary REE‐rich apatite crystallized as allanite and REE‐rich epidote. Magnetite in the ores often occurs as veinlets that cut apatite grains or as anhedral grains that replace a part of augite. These textures suggest that magnetite crystallized in the late stage. Pyrite veins occur in the ores, including a large amount of quartz and calcite veins. Pyrite veins mainly occur with quartz veins in augite. These textures indicate pyrite veins are the latest phase. Apatite–augite–magnetite ore, gabbro–quartz diorite and feldspar dike collected from the Benjamin River prospect contain dirty pure albite (Ab₉₈Or₂–Ab₁₀₀) under the microscope. The feldspar dikes mainly consist of dirty pure albite. Occurrences of the dirty pure albite suggest remarkable albitization (sodic alteration) of original plagioclase (An_25.3–An₆₀ in Pilote et al., 2012) associating with intrusion of monzogranite into gabbro and diorite. SO₄^2? bearing magma crystallized primary REE‐rich apatite, augite and anhydrite reacted with Fe in the sodic fluids, which result in oxidation of Fe²⁺ and release of S^2? into the sodic fluids. REE, Ca and Fe from primary REE‐rich apatite, augite and plagioclase altered by the sodic fluids were released into the fluids. Then Fe³⁺ in the sodic fluids precipitated as Fe oxides and epidote‐group minerals in apatite–augite–magnetite ores. Finally, residual S^2? in sodic fluids crystallized as latest pyrite veins. In conclusion, mineralization in Benjamin River IOA prospect are divided into four stages: (1) oxidized magmatic stage that crystallized apatite, augite and anhydrite; (2) sodic metasomatic stage accompanying alteration of magmatic minerals; (3) oxidized fluid stage (magnetite–epidote group minerals mineralization); and (4) reduced fluid stage (pyrite mineralization).  相似文献   

和(县)含(山)硬石膏矿成因类型、沉积环境及赋矿规律   总被引：2，自引：0，他引：2  

谢长仑  吴承国  苏永荣 《安徽地质》2015,(1):28-34

通过和(县)含(山)硬石膏矿勘查资料,分析研究了该区含矿地层周冲村组(东马鞍山组)岩矿成因类型和代表性剖面岩相划分,认为周冲村组是在早中三叠世缓慢海退和干旱蒸发作用下形成的一套由浅滩—局限海夹潮坪—咸化潟湖—潮上萨布哈的蒸发岩建造,其中的硬石膏矿体主要沉积于咸化潟湖环境;认为早中三叠世的海退和海水咸化过程是循序渐进式发展的,其间发生了许多次小规模海侵或风暴潮,使得咸化潟湖海水的补给和蒸发保持了相对平衡,形成了巨厚硬石膏矿体沉积所需的持续稳定的海水盐度和环境条件;认为早中三叠世的海退有自西向东的退出趋势。同时指出,由于环境差异,本区东部的硬石膏矿品质好于西部。  相似文献   

Genesis of anhydrite in hydrothermally altered basalt from the East Pacific Rise near 13°N     

CHEN Shuai  WANG Xiaoyuan  YIN Xuebo  ZHANG Guoliang 《海洋学报(英文版)》2013,32(2)

  相似文献