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1.
The final ratio equation of an isotopic element in a rock, derived from water/rock formula of McCulloch et al. Earth Planet Sci Lett 46:201-211, 1980, McCulloch et al. J Geophys Res 86:B4 2721-2735, 1981 is used to assess the behavior of diverse suites of rocks towards the alteration effect, and what implications can give about hydrothermal alteration in terms of isotopic compositions. Due to their higher Sr and lower Nd initial ratios than seawater, rocks of metamorphic and sedimentary signatures such as carbonates and Precambrian basement rocks show similar but inverse mixing curves compared with igneous rocks. Sr composition of rocks immediately alters by seawater, while Nd composition keeps unchanged until large volumes of water are added. Although, this can be attributed to the very low Nd concentration in seawater, it indicates that Nd-exchange may only take place under seawater, possibly hydrothermally by circulated seawater, and Nd-concentration of less altered crustal rocks are apparently primary. The isotopic composition and rock mineralogy seem to be the main factors controlling the volume of water required to cause isotopic alteration in rocks. Crustal rocks require higher water volumes due to their relatively low temperature minerals, whereas, mantle peridotites mainly consist of residual olivine minerals that are highly susceptible to alteration and lack of Sr and Nd compositions, and so need less amount of water for metasomatism. This property reduces the limited penetration effect as the mafic affinity increases at depth in the oceanic crust, and enables modified (probably acidified) circulated fluids to maintain ion exchanging and leaching throughout their passageway.  相似文献   

2.
通过对川东地区华蓥山海相三叠系不同岩石类型样品的微观组构、阴极发光和微量元素等分析表明:川东地区华蓥山海相三叠系不同的岩石类型样品具有不同的抵抗成岩蚀变能力,其对海水信息的保存程度也不一致;钙质泥岩所记录的有关信息已基本不能代表海水,多数微晶灰岩所记录的有关信息可以较好地代表海水,而粉晶白云岩只有部分样品可以代表海水的...  相似文献   

3.
Strontium isotope compositions of ancient sulphate deposits not only provide chemostratigraphic information but also offer insight into the system in which the evaporites precipitated. Primary gypsum from two Middle Miocene (Badenian) sections in southern Poland shows steadily higher 87Sr/86Sr ratios than those expected from a marine‐derived formation. The ratios are interpreted as the result of increasing inflow into the basin at the time of gypsum precipitation. Palaeogeographic reconstructions suggest that riverine runoff sources were situated in the West and East European platforms (to the north and east, respectively) and the Carpathians (to the south), which are mostly composed of Mesozoic sedimentary rocks; their dissolution cannot be responsible for the higher 87Sr/86Sr ratios recorded. We conclude that Archaean and Palaeoproterozoic igneous and supracrustal rocks of the Ukrainian Shield were the source of the higher 87Sr/86Sr ratios recorded in the Badenian primary gypsum. A distinctive decreasing trend of 87Sr/86Sr ratios from western Ukraine to southern Poland is explained by a consistent direction of brine inflow during gypsum crystallization (typical cyclonic circulation controlled by the Coriolis effect).  相似文献   

4.
Caliches: Large areas of the northern Sahara and the Algerian High Planes are covered by mostly 1–5 m thick caliches. Their age (Pliocene in the Sahara) decreases to the north and their precipitation is generally independent of groundwater. Their profile is composed (from top to base) as follows:
  • Upper soil, loose and mostly of eolian origin.
  • Upper part of caliche, with very characteristic, dense, partly layered-knobby texture, formed slowly by solutional and reprecipitational processes of ± freely outcropping caliches under addition of eolian material.
  • Under part of caliche, highly porous, somewhat chalky and greyish-white; precipitated mainly by capillar rise of solutions in permeable and calcareous rocks.
  • Substratum, preferentially calcareous sandstones, alluvial deposits and marls.
    • The mineralogy of the caliches (whose main components are represented in fig. 4 A-C) is rather monotonous: in addition to relicts of the substratum (partly dissolved or pushed aside by precipitation of calcite), there are only newly formed low-Mg-calcite and some quarzine (length-slow quartz). Sr-contents of calcite rise clearly from substratum to upper part of caliche. Gypsiferous Crusts (or Cementations): They are found mainly in the surroundings of Chotts (flat, ± saline lakes) and in oases of the NE-Algerian Sahara. Their formation began — mostly caused climatically — after the period of caliche formation and is still continuing in some places. Most of these gypsum-crusts are formed by evaporation of near-surface groundwaters in sandy soils. Water saturated in gypsum precipitates large crystals of gypsum (relatively low in Sr), partly filled by sand, at groundwater-surface. Fine crystalline crusts (relatively high in Sr) are formed by ascendent waters with lower gypsum content ± directly under the landsurface.  相似文献   

    5.
    The porphyritic quartz diorites of the Caledonian Brabant Massif have been totally altered. Ca, Rb, Sr, Zr, Ce, Y measurements and Sr-Nd isotopic analyses were performed on the Quenast plug and the Lessines sill, in an attempt to study the relative mobility of Sr and evaluate the extent, direction and magnitude of the 87Sr/86Sr alterations. Sr electron microprobe analyses of epidote were also carried out to assess its role in the Sr distribution.The initial 87Sr/86Sr ratio is shown to have had an unsteady behaviour during the studied water/rock interactions since it has been sometimes enhanced, sometimes depressed and occasionally not modified. The possibility and magnitude of the 87Sr contamination turn out to be strictly related to the degree of Sr accommodation in the secondary minerals. Epidote in particular has proved to be the main trap for the hydrothermal Sr and this mineral is thus regarded as the major controlling factor of 87Sr hydrothermal contamination. The epidote-poor rocks (albite+chlorite-rich rocks) seem to have been unaffected by any Sr interchange with the aqueous solutions. Therefore, as alteration quickly follows the crystallization of the magma, their initial 87Sr/ 86Sr ratio, which is deduced from an isochron, might be a primary petrogenetic feature enabling interpretation of the genesis of their parental magmas. On the other hand, in the epidote-rich rocks, this ratio has been readily altered; it could thus generally be used only to trace the origin of the hydrothermal solutions. As a consequence, these rocks should not be selected for dating an alteration event by the Rb-Sr method.  相似文献   

    6.
    Ultramafic portions of ophiolitic fragments in the Arabian–Nubian Shield (ANS) show pervasive carbonate alteration forming various degrees of carbonated serpentinites and listvenitic rocks. Notwithstanding the extent of the alteration, little is known about the processes that caused it, the source of the CO2 or the conditions of alteration. This study investigates the mineralogy, stable (O, C) and radiogenic (Sr) isotope composition, and geochemistry of suites of variably carbonate altered ultramafics from the Meatiq area of the Central Eastern Desert (CED) of Egypt. The samples investigated include least-altered lizardite (Lz) serpentinites, antigorite (Atg) serpentinites and listvenitic rocks with associated carbonate and quartz veins. The C, O and Sr isotopes of the vein samples cluster between ?8.1‰ and ?6.8‰ for δ13C, +6.4‰ and +10.5‰ for δ18O, and 87Sr/86Sr of 0.7028–0.70344, and plot within the depleted mantle compositional field. The serpentinites isotopic compositions plot on a mixing trend between the depleted-mantle and sedimentary carbonate fields. The carbonate veins contain abundant carbonic (CO2±CH4±N2) and aqueous-carbonic (H2O-NaCl-CO2±CH4±N2) low salinity fluid, with trapping conditions of 270–300°C and 0.7–1.1 kbar. The serpentinites are enriched in Au, As, S and other fluid-mobile elements relative to primitive and depleted mantle. The extensively carbonated Atg-serpentinites contain significantly lower concentrations of these elements than the Lz-serpentinites suggesting that they were depleted during carbonate alteration. Fluid inclusion and stable isotope compositions of Au deposits in the CED are similar to those from the carbonate veins investigated in the study and we suggest that carbonation of ANS ophiolitic rocks due to influx of mantle-derived CO2-bearing fluids caused break down of Au-bearing minerals such as pentlandite, releasing Au and S to the hydrothermal fluids that later formed the Au-deposits. This is the first time that gold has been observed to be remobilized from rocks during the lizardite–antigorite transition.  相似文献   

    7.
    The Pb-Zn-Ba(-Ag-Au) mineralization in the Triades and Galana mine areas is hosted in 2.5–1.4 Ma pyroclastic rocks, and structurally controlled mostly by NE-SW or N-S trending brittle faults. Proximal pervasive silica and distal pervasive sericite-illite alteration are the two main alteration types present at the surface. The distribution of mineralization-alteration in the district suggests at least two hydrothermal events or that hydrothermal activity lasted longer at Galana. The Sr isotope signature of sphalerite and barite (87Sr/86Sr = 0.709162 to 0.710214) and calculated oxygen isotope composition of a fluid in equilibrium with barite and associated quartz at temperatures of around 230°C are suggestive of a seawater hydrothermal system and fluid/rock interaction. Lead isotope ratios of galena and sphalerite (206Pb/204Pb from 18.8384 to 18.8711; 207Pb/204Pb from 15.6695 to 15.6976; 208Pb/204Pb from 38.9158 to 39.0161) are similar to those of South Aegean Arc volcanic and Aegean Miocene plutonic rocks, and compatible with Pb derived from an igneous source. Galena and sphalerite from Triades-Galana have δ34SVCDT values ranging from +1 to +3.6‰, whereas barite sulfate shows δ34SVCDT values from +22.8 to +24.4‰. The sulfur isotope signatures of these minerals are explained by seawater sulfate reduction processes. The new analytical data are consistent with a seawater-dominated hydrothermal system and interaction of the hydrothermal fluid with the country rocks, which are the source of the ore metals.  相似文献   

    8.
    Located in the western Yangtze Block, the Qingshan Pb–Zn deposit, part of the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic province, contains 0.3 million tonnes of 9.86 wt.% Pb and 22.27 wt.% Zn. Ore bodies are hosted in Carboniferous and Permian carbonate rocks, structurally controlled by the Weining–Shuicheng anticline and its intraformational faults. Ores composed of sphalerite, galena, pyrite, dolomite, and calcite occur as massive, brecciated, veinlets, and disseminations in dolomitic limestones.

    The C–O isotope compositions of hydrothermal calcite and S–Pb–Sr isotope compositions of Qingshan sulphide minerals were analysed in order to trace the sources of reduced sulphur and metals for the Pb–Zn deposit. δ13CPDB and δ18OSMOW values of calcite range from –5.0‰ to –3.4‰ and +18.9‰ to +19.6‰, respectively, and fall in the field between mantle and marine carbonate rocks. They display a negative correlation, suggesting that CO2 in the hydrothermal fluid had a mixed origin of mantle, marine carbonate rocks, and sedimentary organic matter. δ34S values of sulphide minerals range from +10.7‰ to +19.6‰, similar to Devonian-to-Permian seawater sulphate (+20‰ to +35‰) and evaporite rocks (+23‰ to +28‰) in Carboniferous-to-Permian strata, suggesting that the reduced sulphur in hydrothermal fluids was derived from host-strata evaporites. Ores and sulphide minerals have homogeneous and low radiogenic Pb isotope compositions (206Pb/204Pb = 18.561 to 18.768, 207Pb/204Pb = 15.701 to 15.920, and 208Pb/204Pb = 38.831 to 39.641) that plot in the upper crust Pb evolution curve, and are similar to those of Devonian-to-Permian carbonate rocks. Pb isotope compositions suggest derivation of Pb metal from the host rocks. 87Sr/86Sr ratios of sphalerite range from 0.7107 to 0.7136 and (87Sr/86Sr)200Ma ratios range from 0.7099 to 0.7126, higher than Sinian-to-Permian sedimentary rocks and Permian Emeishan flood basalts, but lower than Proterozoic basement rocks. This indicates that the ore strontium has a mixture source of the older basement rocks and the younger cover sequence. C–O–S–Pb–Sr isotope compositions of the Qingshan Pb–Zn deposit indicate a mixed origin of the ore-forming fluids and metals.  相似文献   

    9.
    Recent studies on mineralogy, geochronology, fluid inclusion and stable isotope (Pb, Os, S, C, O, Sr) characteristics were reviewed to determine constraints for genetic models of the Chilean manto‐type copper deposits. The Chilean manto‐type deposits are divided into the two geologic categories of the northern areas (Arica–Iquique, Tocopilla–Taltal) and the central areas (Copiapó, La Serena, Santiago). The former is distributed in the coastal range composed of Jurassic andesite‐dominated volcano‐sedimentary piles and younger plutonic intrusions, and yields chalcocite (‐digenite) and bornite as the principal hypogene copper sulfides. The latter is hosted mostly in Lower Cretaceous volcano‐sedimentary sequences, and has chalcopyrite‐rich mineral associations. The fluid inclusion data indicate that the primary copper mineralization was commonly generated in the temperature range 150–360°C under low‐pressure conditions near the boiling curve, mediated with relatively saline brines. Generally, homogeneous Pb and S isotope compositions for primary copper minerals imply direct magma source or leaching of igneous rocks. Pb and Os isotope data published for some deposits, however, suggest that ore‐forming metals were derived mainly from the volcano‐sedimentary host rocks. The noticeably negative isotope ratios of primary sulfide sulfur and hydrothermal calcite carbon of some central area deposits indicate influx of sedimentary rock components, and the high 87Sr/86Sr initial ratios of hydrothermal calcite from the Tocopilla–Taltal area deposits imply contribution of the contemporaneous seawater or marine carbonates. These isotopic constraints imply a formation mechanism in which the Chilean manto‐type copper deposits formed epigenetically in the process of hydrothermal interaction of non‐magmatic surface‐derived brine with the volcano‐sedimentary host rocks, which is inferred to have been induced by a deep‐seated plutonic complex as the possible heat source.  相似文献   

    10.
    Neodymium, Sr and Pb isotopic compositions, along with rare earth element (REE) concentrations were determined for twelve black ores and one yellow ore from twelve localities of the Kuroko deposits, Japan. The ores were generated by submarine hydrothermal activity during the Miocene age. Neodymium isotopic compositions of the ores (Nd: –4.9 to +6.5) mostly overlap with spatially associated igneous rocks. On a Nd versus Sr isotopic correlation diagram, however, 87Sr/86Sr ratios are shifted from the associated igneous rocks towards the higher contemporaneous seawater ratio. REE patterns are highly variable, ranging from light REE enriched to depleted, and show no Ce anomalies, as would be expected if they were derived from seawater. These results suggest that the REEs contained in ores were mainly derived from the associated igneous rocks, but that the ore Sr is a mixture derived from both seawater and the igneous rocks. Most Pb isotopic compositions fall within the range defined by the associated igneous rocks (206Pb/204Pb=18.35–18.84, 207Pb/204Pb=15.59–15.97 and 208Pb/204Pb=38.53–39.90), although several samples have very radiogenic compositions that were most likely derived from basement rocks. Our new Pb isotopic results display greater variation, and have a larger range of more radiogenic compositions than has been noted previously for these ores. In addition, the black ore with the most radiogenic Pb isotopic composition also has the least radiogenic Nd isotopic composition. This suggests that at least some of the Pb contained in the ores was derived mainly from older basement rocks. The large positive Eu anomalies for some black ores are consistent with a high-temperature origin for the parental fluids, irrespective of the source rock. The single yellow ore examined, however, has a small negative Eu anomaly, which may indicate derivation from a lower temperature fluid. Previous studies suggested that the Kuroko ores were formed in the presence of organic materials in an anoxic basin. Combined Nd, Sr, Pb and Os isotopic and REE abundance data indicate that multiple sources were involved in the genesis of Kuroko ores.  相似文献   

    11.
    锶同位素已经成为全球海平面变化、造山运动、古气候和古环境等全球地质事件研究与对比的有效工具之一。本文以四川盆地东部地区早中三叠世蒸发岩的野外剖面和钻孔岩心为主要研究对象,测试了碳酸盐岩、硫酸盐岩和石盐岩的锶同位素组成,并建立了相应的锶同位素演化曲线。研究结果显示,碳酸盐岩的87Sr/86Sr值平均为0.707 895,硬石膏岩的87Sr/86Sr值平均为0.708 174,石盐岩的87Sr/86Sr值平均为0.708 177,同时碳酸盐岩的87Sr/86Sr值从早三叠世的0.707 413快速增加到中三叠世早期的0.708 515,而后呈现下降趋势。从总体上看,这些87Sr/86Sr值与全球早中三叠世同期的87Sr/86Sr值数据接近,说明四川盆地东部地区早中三叠世钾盐的物质来源大部分为海水,并沉积于海相沉积环境,同时由于火山...  相似文献   

    12.
    Comprehensive data on the chemical composition of reservoir rocks and geothermal brines from the geothermal well doublet Groβ Schönebeck (North German Basin) drilled into a Rotliegend sedimentary and Permo-Carboniferous volcanic rock reservoir were sampled over the past years. They were characterized with respect to their major and minor elemental composition including various isotope ratios. The study considered the impact of drilling and reservoir operations on fluid composition and aimed at determining fluid–rock interactions to gain information on fluid origin and hydraulic pathways.The highly saline fluids (up to 265 g/L TDS) show δ 18O and δD of water (2.7–5.6 and −3.1–15, respectively) as well as δ 34S of sulfate (3.6–5), and 87Sr/86Sr ratios (0.715–0.716) that resemble Rotliegend brines from an area located around 200 km in the west (the Altmark). Halogen ratios indicated that brines developed predominantly by evaporation of meteoric water (primary brine) together with halite dissolution brine (secondary brine). Indication for mixing with Zechstein brine or with younger meteoric water was not found.No geochemical distinction was possible between fluids deriving from different rock formations (dacites or sedimentary rocks, respectively). This is due to the evolution of the sediments from the effusive rocks resulting in a similar mineralogical and chemical composition and due to a hydraulic connectivity between the two types of rock. This connection existed probably already before reservoir stimulation as indicated by a set of faults identified in the area that could connect the Rotliegend formation with both, the volcanic rocks and the lower units of the Zechstein. Additional geochemical indication for a hydraulic connectivity is given by (1) the very high heavy metal contents (mainly Cu and Pb) in fluids and scaling that derive from the volcanic rocks and were that were also found in increased amounts up at the Zechstein border (Kupferschiefer formation). (2) The 87Sr/86Sr isotope ratios of fluid samples correspond to the ratios determined for the sedimentary rocks indicating that initially the fluids developed in the sedimentary rocks and circulated later, when faults structures were created by tectonic events into the volcanic rocks.  相似文献   

    13.
    The salt waters from the Emilia-Romagna sector of the Northern Apennine Foredeep have been investigated using major and trace element and stable isotope (δ2H, δ18O, δ37Cl, δ81Br and 87Sr/86Sr ratio). Ca, Mg, Na, K, Sr, Li, B, I, Br and SO4 vs. Cl diagrams suggest the subaerial evaporation of seawater beyond gypsum and before halite precipitation as primary process to explain the brine’s salinity, whereas saline to brackish waters were formed by mixing of evaporated seawater and water of meteoric origin. A diagenetic end-member may be a third component for mud volcanoes and some brackish waters. Salinization by dissolution of (Triassic) evaporites has been detected only in samples from the Tuscan side of the Apennines and/or interacting with the Tuscan Nappe. In comparison with the seawater evaporation path, Ca–Sr enrichment and Na–K–Mg depletion of the foredeep waters reveal the presence of secondary processes such as dolomitization–chloritization, zeolitization–albitization and illitization. Sulfate concentration, formerly buffered by gypsum-anhydrite deposition, is heavily lowered by bacterial and locally by thermochemical reduction during burial diagenesis. From an isotopic point of view, data of the water molecule confirm mixing between seawater and meteoric end-members. Local 18O-shift up to +11‰ at Salsomaggiore is related to water–rock interaction at high temperature (≈150°C) as confirmed by chemical (Mg, Li, Ca distribution) and isotopic (SO4–H2O) geothermometers. 37Cl/35Cl and 81Br/79Br ratios corroborate the marine origin of the brines and evidence the diffusion of halogens from the deepest and most saline aquifers toward the surface. The 87Sr/86Sr ratio suggests a Miocene origin of Sr and rule out the hypothesis of a Triassic provenance of the dissolved components for the analyzed waters issuing from the Emilia-Romagna sector of the foredeep. Waters issuing from the Tuscan side of the Apennines and from the Marche sector of the foredeep show higher 87Sr/86Sr ratios because of the interaction with siliciclastic rocks.  相似文献   

    14.
    The Sr isotopic composition of sediment-hosted magnesites in Permian and Scythian series of Upper Austroalpine units (Eastern Alps) has been determined. The results suggest diagenetic-metasomatic magnesite formation by Mg-rich pore solutions. The depositional environment of the magnesite-bearing rocks is reflected by different isotopic compositions with initial 87Sr/86Sr ratios close to contemporaneous sea water in marine sediments (0.7071–0.7083) and higher ratios being typical for lacustrine and coastal environments influenced from the hinterland (0.7133–0.7139). Coarser grained recrystallized magnesite and magnesite veins show a distinct increase in their Sr isotopic ratios (0.7202–0.7220) which can be attributed to metamorphic fluids of Eoalpine age. The findings of these magnesite occurrences, which have been affected only by very low-grade metamorphism, are compared with similar results from spar magnesites associated with metamorphosed Paleozoic sedimentary rocks. A similar genetic model is proposed for the first magnesite mineralization in those Paleozoic strata, but with variably intense later recrystallisation during metamorphism.  相似文献   

    15.
    安徽伏川蛇绿岩套的Nd-Sr-O同位素研究   总被引：13，自引：1，他引：13       下载免费PDF全文
    安徽歙县伏川的蛇绿岩套形成于中-晚元古宙,其Nd、Sr和O同位素组成是:εNd(T)=+0.7-+3.8,εSr(T)=+30.7-+53.9,δ18O=3.2-11.0‰。据地质学和同位素地球化学特征,该岩套位于杨子板块南缘、江南古岛弧的弧后小洋盆地轴部。εNd(T)值的变化是由于蛇绿岩形成过程中受到下伏不成熟硅铝质基底地壳的混染引起的;εSr(T)和δ18O的变化,是在蛇绿岩形成时或形成后不久遭受海水热液蚀变的结果。  相似文献   

    16.
    The Mont-de-l’Aigle deposit is located in the northern part of Dome Lemieux, in the Connecticut Valley-Gaspé Synclinorium, Gaspé Peninsula, Québec. The Dome Lemieux is a subcircular antiform of Siluro–Devonian sedimentary rocks that is cut by numerous mafic and felsic sills and dikes of Silurian to Late Devonian age. Plutonism occurred in a continental within-plate extensional setting typical of orogenic collapse. The Cu−Fe (± Au) mineralization of Mont-de-l’Aigle occurs in veins, stockworks, and breccias. Mineralization is located near or within N−S and NW−SE faults cutting sedimentary rocks. IOCG mineralization postdates intrusions, skarns, hornfels, and epithermal mineralization typical of the southern part of the Dome Lemieux. The paragenetic sequence comprises: (1) pervasive sodic, potassic, chlorite, and silica alteration, (2) hematite, quartz, pyrite, magnetite, and chalcopyrite veins, stockworks and breccias and, (3) dolomite ± hematite veins and veinlets cutting the earlier mineralization. Intrusions display proximal sodic and potassic alteration, whereas sedimentary rocks have proximal decalcification, silicification, and potassic alteration. Both intrusive and sedimentary rocks are affected by a pervasive distal chlorite (± silica) alteration. The sulfur isotope composition of pyrite and chalcopyrite (δ34S=−1.5 to 4.8‰) suggests that sulfur was derived mainly from igneous rocks. Fluid δ18O (−0.4 to 2.65‰) indicates meteoric or seawater that reacted with the country rocks. Mixing of hot magmatic fluids with a cooler fluid, perhaps meteoric or seawater is suggested for mineral deposition and alteration of the Mont-de-l’Aigle deposit. The mineralogy, alteration, and sulfur isotope composition of the Mont-de-l’Aigle deposit compare well with IOCG deposits worldwide, making the Mont-de-l’Aigle deposit a rare example of Paleozoic IOCG mineralization, formed at shallow depth, within a low metamorphic grade sedimentary rock sequence.  相似文献   

    17.
    In the Eastern Pontide Region of northeastern Turkey, volcanogenic Cu-Zn-Pb deposits of the Kuroko type are widespread within the dacitic series of the Liassic-Eocene volcano-sedimentary succession. Sulfide mineralization within the studied deposits shows four different depositional styles: disseminated ore; polymetallic stockwork ores; polymetallic massive ores; and disseminated pyrite in the hanging-wall tuff units. Only the stockwork and massive ores are economically important, and usually one or the other dominates in each ore body.

    The δ34S of sulfide minerals belonging to the various styles of mineralization are in the range from ?2.6 to +5.2% (VCDT): pyrite has the highest values and the galena lowest values in agreement with the usual isotopic-fractionation trends. Massive ores have heavier sulfur-isotope composition among the mineralization styles and the heaviest values are recorded in barite- and gypsum-rich deposits. The close similarity of the δ34S among the various mineralization episodes in some deposits indicates a single sulfur source having a stable and homogenous composition.

    The δ34S of sulfates fall into three groups: barites and primary gypsum (15.4 to 20.4%), close to coeval seawater sulfate; one value of barite (25.4%) heavier than coeval sea water; and values of secondary gypsum (2.2 to 8.0%) either very light compared to coeval seawater sulfate, or within the range recorded from sulfide minerals. The δ34S values of pyrite disseminated in the brecciated dacite tuff units are very close to zero and similar to the ones reported for magmatic rocks, suggesting a magmatic source for the sulfur of the earliest sulfide mineralization episode. These δ34S data are not sufficient to calculate the fraction of the reduced sulfur derived from seawater sulfate, as the associated fractionation factor cannot be constrained.  相似文献   

    18.
    Abundant veins filled by calcite, celestite and pyrite were found in the core of a 719 m deep borehole drilled in Oftringen near Olten, located in the north-western Molasse basin, close to the thrust of the Folded Jura. Host rocks are calcareous marl, argillaceous limestone and limestone of the Dogger and Malm. The δ18O values of vein calcite are lower than in host rock carbonate and, together with microthermometric data from fluid inclusions in vein calcite, indicate precipitation from a seawater-dominated fluid at average temperatures of 56–68°C. Such temperatures were reached at the time of maximum burial of the sedimentary pile in the late Miocene. The depth profile of δ13C and 87Sr/86Sr values and Sr content of both whole-rock carbonate and vein calcite show marked trends towards negative δ13C, high 87Sr/86Sr, and low Sr content in the uppermost 50–150 m of the Jurassic profile (upper Oxfordian). The 87Sr/86Sr of vein minerals is generally higher than that of host rock carbonate, up to very high values corresponding to Burdigalian seawater (Upper Marine Molasse, Miocene), which represents the last marine incursion in the region. No evidence for internally derived radiogenic Sr (clay minerals) has been found and so an external source is required. S and O isotope composition of vein celestite and pyrite can be explained by bacterial reduction of Miocene seawater sulphate. The available data set suggests the vein mineralization precipitated from descending Burdigalian seawater and not from a fluid originating in the underlying Triassic evaporites.  相似文献   

    19.
    Hydrothermal convection initiated by emplacement of the gabbro-syenite complex of Abu Khruq into the Egyptian basement 89 Ma ago systematically altered the trace element and isotopic compositions of the syenites. The scale of Sr transport in migrating solutions was far larger than the scale of Sr isotopic equilibration within rocks. As a result, Sr exchange was heterogeneous in the syenites, an effect which can be observed on three different scales. Within grains of a single mineral species, heterogeneities are related to grain boundaries and microfractures through which fluids migrated. Among minerals within rock samples, heterogeneities are related to differences in susceptibility to Sr alteration. Among samples within a single unit, heterogeneous alteration is apparently related to differences in permeability close to fracture zones.During the early stages of alteration radiogenic Sr derived from the country rocks was added to the syenites, causing small net changes in concentration (5 ppm ave.). Some Rb-Sr mineral isochrons from single rock samples yield the emplacement age because isotopic equilibration of this added Sr sometimes occurred within rock specimens. However, regressions of the whole-rock Rb-Sr data yield apparent ages that are about 10 Ma too old. Later stage alteration involved larger changes in whole-rock Sr concentration (45 ppm ave.) but had little further effect on the isotopic relationships because the Sr was derived from cogenetic gabbros rather than the country rocks.Alterations of Rb, Sr, and Sr isotopic compositions are not well correlated with changes in 18O/16O ratio because mineralogy played an important role in decoupling trace element and oxygen isotopic alteration. In general, the absence of such correlations for whole-rock data is not diagnostic of rocks with unaltered trace element and isotopic compositions. Mineral-scale Sr isotopic heterogeneities associated with grain boundaries and microfractures may be the most unambiguous evidence of trace element mobility.Deceased on 9/81  相似文献   

    20.
    The Sr and C isotopic compositions of Precambrian carbonate rocks are determined for Amderma Rise, in the northeastern margin of Pai-Khoi Ridge. Based on the Sr isotopic chemostratigraphy, it is established for the first time that the Amderma Formation is referred to the Early Vendian, while the Morozovsk Formation is Late Riphean in age. This conclusion along with detailed mapping proves that the Precambrian “section” of the Amderma Rise is a series of tectonic plates combined in a nonchronostratigraphic order. Volcanic and sedimentary rocks of the Morozovsk and Sokolninsk formations make up the allochthon proper, while carbonate rocks of the Amderma Formation make up the para-autochthon. The high values of δ13С (up to +9.5‰) identified in limestones of both formations suggest a considerable distance of the Pai-Khoi paleobasin from the passive margin of the Baltic Region upon facies similarity to the Laurentia active margins.  相似文献   

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