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1.
The mineralogy and structure of the supergene profile in recently-exploited volcaniс hosted massive sulphide (VHMS) deposits of Cyprus, Uralian and Kuroko type in the South Urals, Russia, have been studied. Specific subzones enriched in secondary sulphides and associated minerals have been distinguished in residual pyrite and quartz–pyrite sands at the Gayskoye, Zapadno-Ozernoye, Dzhusinskoye and Alexandrinskoye deposits. Besides minerals which are common to the cementation subzones (covellite, chalcocite and acanthite), non-stoichiometric colloform and framboidal pyrite, pyrite–dzharkenite, pyrrhotite-like and jordanite-like minerals, metacinnabar, sphalerite, selenium-enriched tetrahedrite and unidentified As-, Sb sulphosalts of Pb or Hg and Ag, sulphur-bearing clausthalite, naumannite and tiemannite were also found. Secondary sulphide minerals in VHMS deposits of the South Urals region are characterized by light sulphur isotope compositions (− 8.1 to − 17.2‰). Superposition of the advanced oxidation of colloform pyrite, an enrichment in impurities (sphalerite, galena, and tennantite) from the primary ores, stagnant water conditions, an elevation of the water table during oxidation, and bacterial activity led to supergene concentrations of the base metals as sulphide, selenides or sulphosalts.  相似文献   

2.
Petrological data provide evidence that framboidal pyrite, Fe-carbonates and kaolinite are the major diagenetic minerals developed during burial diagenesis in the Tertiary Niger Delta sandstones and associated mudrocks. The pyrite sulphur, carbonate carbon and oxygen and kaolinite oxygen and hydrogen isotope compositions have been determined. These data (pyrite, δ34S = −24.8 to 21.0‰; “siderite”, δ13C(PDB) = −14.7 to +5.0‰, δ18O(PDB) = −19.1 to −0.6‰; Fe-calcite, δ13C(PDB) = +17.5 to 17.9‰, δ18O(PDB) = −8.3 to −8.0‰; kaolinite, δ18O(SMOW) = +14.7 to 17.5‰, δD (SMOW) = −86 to −43‰) have been used to interpret the isotopic compositions of the precipitating pore fluids and/or the temperatures of mineral formation. The interpretation of these results indicate that in the deltaic depositional setting the syndepositional pore waters had a significant but variable marine influence that favoured the early formation of pyrite. Subsequently the subsurface influence of meteoric waters, showing varying degrees of modification involving organic and/or water-rock reactions, played an increasingly significant role in the development of later diagenetic cements in the sediments when abundant authigenic carbonates and kaolinites were formed.  相似文献   

3.
The Daduhe gold field comprises several shear-zone-controlled Tertiary lode gold deposits distributed at the eastern margin of the Tibetan Plateau. The deposits are hosted in a Precambrian granite–greenstone terrane within the Yangtze Craton. The gold mineralization occurs mainly as auriferous quartz veins with minor sulphide minerals. Fluid inclusions in pyrite have 3He/4He ratios of 0.16 to 0.86 Ra, whereas their 40Ar/36Ar ratios range from 298 to 3288, indicating a mixing of fluids of mantle and crust origins. The δ34S values of pyrite are of 0.7–4.2‰ (n = 12), suggesting a mantle source or leaching from the mafic country rocks. δ18O values calculated from hydrothermal quartz are between − 1.5‰ and + 6.0‰ and δD values of the fluids in the fluid inclusions in quartz are − 39‰ and − 108‰. These ranges demonstrate a mixing of magmatic/metamorphic and meteoric fluids. The noble gas isotopic data, along with the stable isotopic data suggest that the ore-forming fluids have a dominantly crustal source with a significant mantle component.  相似文献   

4.
The sulphide-bearing rocks of the Upper Cretaceous Germav Formation in southeastern Turkey (Bozova–Urfa) and the morphologically varied sulphide occurrences they contain have been investigated. Pyrite and marcasite are the main sulphide minerals; lesser bravoite and millerite also occur. Pyritised branches and leaves, trace fossils, and animal microfossils and macrofossils are abundant. Most of the concretionary and authigenic concretionary pyrite occurrences are probably related to burrows. The concretionary pyrites have low Co and high Ni contents and low Co:Ni ratios. The pyrite-rich lithostratigraphic sequences were deposited in a deep-sea environment, and pyrite mineralization developed in syn-sedimentary, early diagenetic and epigenetic stages under anoxic conditions. To cite this article: C. Bölücek, B. Ilhan, C. R. Geoscience 338 (2006).  相似文献   

5.
A distinct vertical zonation very similar to that described for the Kuroko deposits of Japan, is displayed by both mineralogy and textures of sulphides from the Lahanos and Kzlkaya massive sulphide deposits of northeastern Turkey. A deeper erosional level is exposed at the Kzlkaya deposit, so that only remnants of the massive sulphide ore zone are present. The zonation is from an upper zone of massive Cu and Zn sulphides (black and yellow ore) with fine-grained, colloform, banded, framboidal, and spherulitic textures, downwards through an intermediate zone of low Cu-Zn massive pyrite with transitional textures, to a lower zone of stockwork and impregnated pyrite displaying euhedral, zoned textures. The fine-grained and colloform pyrite of the upper zones is progressively overgrown by, and recrystallized to, the massive and euhedral pyrite of lower zones. The original textures of these deposits are best preserved by pyrite. The previous interpretation of these textures, of sulphide deposition from colloidal solutions ponded by an impermeable pyroclastic horizon, is reexamined in the light of present observations. Although ultra-fine-grained sulphides, framboids, and radially-cracked spherules could have formed by replacement of pre-existing minerals by a colloidal solution, the colloform and banded textures are indicative of growth in open spaces. It thus seems likely that the fine-grained colloform sulphides, including chalcopyrite, sphalerite, and tennantite as well as pyrite, were initially deposited on or near the surface of the sea-floor. Additional evidence for this interpretation is seen in the progressive recrystallization of the sulphide textures to massive, much coarser, pyrite in the lower zones. This recrystallization may in part be due to diagenetic and hydrothermal processes operating after formation of the original layered sulphides. These conclusions are in agreement with those reached for the similar, but larger Madenköy deposit 100 km to the east.  相似文献   

6.
Concentrations of iron sulphide minerals in sediments within and adjacent to a small intertidal thermal pool near Talasea township are forming and being modified under a wide range of exhalative-sedimentary conditions. A geochemical, mineralogical and bacteriological investigation of these iron sulphides has defined the major reactions leading to their formation and indicated aspects in which their mineralogies, textures and mechanisms of formation differ significantly from those of iron sulphides formed under “normal” sedimentary conditions. The main features of the thermal pool environment are: 1. the occurrence of relatively high iron sulphide concentrations; 2. the preservation, by the strongly anaerobic thermal spring waters, of hydrotroilite formed in the thermal pool sediments in the presence of excess sulphide; 3. the presence in the pool banks of major marcasite (which appears to replace its dimorph pyrite) formed as a result of the development of strongly acidic conditions; 4. the abundance in the pool banks of large euhedral crystals of pyrite and marcasite, and the scarcity of framboids; 5. the presence of sulphate-reducing bacteria in the thermal waters and sediments.  相似文献   

7.
The carbonate-hosted Kabwe Pb–Zn deposit, Central Zambia, has produced at least 2.6 Mt of Zn and Pb metal as well as minor amounts of V, Cd, Ag and Cu. The deposit consists of four main epigenetic, pipe-like orebodies, structurally controlled along NE–SW faults. Sphalerite, galena, pyrite, minor chalcopyrite, and accessory Ge-sulphides of briartite and renierite constitute the primary ore mineral assemblage. Cores of massive sulphide orebodies are surrounded by oxide zones of silicate ore (willemite) and mineralized jasperoid that consists largely of quartz, willemite, cerussite, smithsonite, goethite and hematite, as well as numerous other secondary minerals, including vanadates, phosphates and carbonates of Zn, Pb, V and Cu.Galena, sphalerite and pyrite from the Pb–Zn rich massive orebodies have homogeneous, negative sulphur isotope ratios with mean δ34SCDT permil (‰) values of − 17.75 ± 0.28 (1σ), − 16.54 ± 0.0.27 and − 15.82 ± 0.25, respectively. The Zn-rich and Pb-poor No. 2 orebody shows slightly heavier ratios of − 11.70 ± 0.5‰ δ34S for sphalerite and of − 11.91 ± 0.71‰ δ34S for pyrite. The negative sulphur isotope ratios are considered to be typical of sedimentary sulphides produced through bacterial reduction of seawater sulphate and suggest a sedimentary source for the sulphur.Carbon and oxygen isotope ratios of the host dolomite have mean δ13CPDB and δ18OSMOW values of 2.89‰ and 27.68‰, respectively, which are typical of marine carbonates. The oxygen isotope ratios of dolomite correlate negatively to the SiO2 content introduced during silicification of the host dolomite. The depletion in 18O in dolomite indicates high temperature fluid/rock interaction, involving a silica- and 18O-rich hydrothermal solution.Two types of secondary fluid inclusions in dolomite, both of which are thought to be related to ore deposition, indicate temperatures of ore deposition in the range of 257 to 385 and 98 to 178 °C, respectively. The high temperature fluid inclusions contain liquid + vapour + solid phases and have salinities of 15 to 31 eq. wt.% NaCl, whereas the low temperature inclusions consist of liquid + vapour with a salinity of 11.5 eq. wt.% NaCl.Fluid transport may have been caused by tectonic movements associated with the early stages of the Pan-African Lufilian orogeny, whereas ore deposition within favourable structures occurred due to changes in pressure, temperature and pH in the ore solution during metasomatic replacement of the host dolomite. The termination of the Kabwe orebodies at the Mine Club fault zone and observed deformation textures of the ore sulphides as well as analysis of joint structures in the host dolomite, indicate that ore emplacement occurred prior to the latest deformation phase of the Neoproterozoic Lufilian orogeny.  相似文献   

8.
Petrographic and sulphur isotope studies support the long‐held contention that rounded grains of pyrite in siliciclastic sequences of the Late Archaean Witwatersrand Supergroup originated as placer grains. The grains are concentrated at sites where detrital heavy minerals are abundant within quartz‐pebble conglomerates and quartzose sandstones. Depositional sites with abundant pyrite are: (1) within the matrix of bar‐type, clast‐supported conglomerates; (2) on scoured or winnowed surfaces; and (3) on stratification planes. The grains are internally compact or porous, with truncation of internal structure at outer margins indicating fragmentation and rounding of pyritic source‐rocks during erosion and sediment transport. A large range in textures reflects source‐rock lithologies, with known varieties linked to sedimentary‐hosted diagenetic pyrite, volcanic‐hosted massive sulphide deposits and hydrothermal pyrite. Laser ablation sulphur isotope analysis of pyrite reveals a broader range in δ34S values (? 5·3 to + 6·7‰) than that of previously reported conventional bulk‐grain analyses (? 1 to + 4‰). Rounded pyrite from the Steyn Reef has significant variation in δ34S values (? 4·7 to + 6·7‰) that establishes heterogeneous sulphur compositions, with even adjacent grains having diverse isotopic signatures. The heterogeneity supports a placer origin for rounded pyrite. Euhedral pyrite and pyrite overgrowths which are undoubtedly authigenic have restricted δ34S values (? 0·5 to + 2·5‰), are chemically distinct from rounded pyrite and are probably the products of metamorphism or hydrothermal alteration. The placer origin of rounded pyrite indicates that pyrite was a stable heavy mineral during erosion and transport in the early atmosphere. Its distribution in three sequences (Witwatersrand Supergroup, Ventersdorp Contact Reef and Black Reef), and in other sequences not linked to Witwatersrand‐type Au‐U ore deposits, implies deposition of redox‐sensitive detrital heavy minerals during the Late Archaean. Consequently, rounded grains of detrital pyrite are strong indicators of an oxygen‐poor atmosphere. While not confirming a placer origin for gold in Witwatersrand Au‐U ore deposits, the palaeoenvironmental significance of rounded pyrite negates its link to hydrothermal mineralization.  相似文献   

9.
Located at western portion of northern margin of North China craton, the Baotou–Bayan Obo district is one of the most important Fe–REE–Nb and Au metallogenic provinces in China. Presently, about 52 gold deposits and prospects have been discovered, explored and mined, among which Shibaqinhao, Laoyanghao, Houshihua, Saiyinwusu, Wulashan and Donghuofang are the most important ones. All these gold occurrences can be subdivided into three groups (or types) according to its host rocks: (1) hosted by Archean high-grade metamorphic rocks; (2) hosted by Proterozoic sedimentary rocks; (3) hosted by or related to Hercynian alkaline intrusive rocks. The first group contains the Shibaqinhao, Laoyanghao and Houshihua gold deposits. Gold mineralization at these three deposits occurs within Archean amphibolite, gneiss and granulite as gold-bearing quartz veins and veinlet groups containing native gold, electrum, pyrite and chalcopyrite. The Saiyinwusu deposit belongs to the second group, and occurs within Proterozoic sandstone, quartzite and carbonaceous slate as quartz veins and replacement bodies along the fracture zones. Pyrite, marcasite, arsenopyrite, native gold and electrum are identified. The third group includes the Wulashan, Donghuofang and Luchang deposits. Gold mineralization at these three deposits occurs predominantly within the Hercynian alkaline syenite or melagabbro stocks and dyke swarms or along their contacts with Archean metamorphic wall rocks as K-feldspar–quartz veins, dissemination and veinlets. Pyrite, galena, chalcopyrite, native gold and calaverite are major metallic minerals.δ34S value of sulfides (pyrite, galena and pyrrhotite) separates from groups 1 and 2 varies from −4.01‰ to −0.10‰ and −3.01‰ to 2.32‰, respectively. δ34S values of Archean and Proterozoic metamorphic wall rocks for groups 1 and 2 deposits range from −20.2‰ to −17.0‰ and −15.8‰ to −16.2‰, respectively. The values are much lower than their hosted gold deposits. All these pyrite separates from Hercynian alkaline intrusions associated with the gold deposits show positive δ34S values of 1.3‰ to 4.8‰, which is higher than those Precambrian metamorphic wall rocks and their hosted gold deposits. δ34S values of the sulfides (pyrite and galena) from the Donghuofang and Wulashan deposits (group 3) increase systematically from veins (−14.8‰ to −2.4‰) to the Hercynian alkaline igneous wall rocks (2.8‰ to 4.8 ‰). All of these deposits in groups 1, 2 and 3 show relatively radiogenic lead isotopic compositions compared to mantle or lower crust curves. Most lead isotope data of sulfides from the gold ores plot between the Hercynian alkaline intrusions and Precambrian metamorphic wall rocks. Data are interpreted as indicative of a mixing of lead from mantle-derived alkaline magma with lead from Precambrian metamorphic wall rocks.Isotopic age data, geological and geochemical evidence suggest that the ore fluids for the groups 1 and 2 deposits were generated during the emplacement of the Hercynian alkaline syenite and mafic intrusions. The Hercynian alkaline magma may provide heat, volatiles and metals for these groups 1 and 2 deposits. Evolved metamorphic fluids produced by the devolatilization, which circulated the wall rocks, were also progressively involved in the alkaline magmatic hydrothermal system, and may have dominate the ore fluids during late stage of ore-forming processes. Most of these gold deposits hosted by Archean high-grade metamorphic rocks occur at or near the intersections of the NE- and E–W-trending fracture systems. The ore fluid of the group 3 deposits may have resulted from the mixing of Hercynian alkaline magmatic fluids and evolved meteoric waters. The deposits are believed to be products of Hercynian alkaline igneous processes along deep-seated fault zones within Archean terrain.  相似文献   

10.
Gold paleoplacers become progressively more affected by diagenetic processes with age and burial. Mesozoic paleoplacer deposits in southern New Zealand display intermediate stages of diagenetic transformation compared to little-affected Late Cenozoic paleoplacers and strongly-affected Paleozoic and Precambrian paleoplacers. The Mesozoic (Cretaceous) diagenesis resulted in near-pervasive alteration, cementation and lithification of the paleoplacer. Lithic clasts and matrix have been extensively altered to illite, ferrous iron-bearing smectite-vermiculite, and kaolinite, and the cement consists mainly of clays and calcite. Diagenetic pyrite, marcasite, vivianite, and Mn oxide also contributed to cementation. Alteration occurred under near-surface (<500 m depth) conditions with groundwater that had circumneutral pH, high alkalinity, and elevated dissolved K, Mg and Ca. Detrital albite remained unaffected by alteration. Detrital gold has been variably dissolved and redeposited, with widespread formation of gold overgrowths on the 1–10 μm scales, with 1–3 wt% Ag. Gold mobility was driven by reduced sulphur complexes in the low redox, high pH diagenetic environment. The overgrowth gold locally contributed to cementation of fine clastic grains, and has intergrown with diagenetic clays and Mn oxide. Post-diagenetic oxidation of the paleoplacer deposit has transformed much of the pyrite to ferric oxyhydroxide and deposited some ferric oxyhydroxide coatings on gold. These oxidation processes have had only minor effects on gold mobility and textures. Hence, the low redox conditions of diagenetic gold mobility were distinctly different from those typically associated with oxidation-related supergene gold mobility. Diagenesis can affect economics of paleoplacer mining by hindering rock disaggregation during processing, coating gold particles with secondary minerals, and increasing the clay content of the deposit, all of which can lower the efficiency of gold recovery.  相似文献   

11.
Heavy mineral separates of peat from a mineralotrophic bog contain sulphide minerals with distinctive textures. Pyrite framboids, consisting of spherical aggregates of subhedral pyrite crystals, are surrounded by a thin rim of chalcopyrite or a layer of massive marcasite. Clusters of framboids are cemented by covellite which also occurs as small idiomorphic grains, with rectangular or hexagonal outlines, surrounded by chalcopyrite. The sulphides appear to have resulted from discharge of groundwaters, enriched in copper from weathering of primary sulphides in bedrock and in iron by reduction of the till underlying the peat, into the hydrogen sulphide charged bog.  相似文献   

12.
Mike Solomon   《Ore Geology Reviews》2008,33(3-4):329-351
The Ordovician Zn–Pb–Cu massive sulphide ore deposits of the Bathurst mining camp share many features with those of the Devonian/Carboniferous Iberian pyrite belt, particularly the tendency to large size (tonnage and metal content); shape, as far as can be determined after allowing for deformation; metal content, particularly Fe/Cu, Pb/Zn and Sn; mineral assemblages (pyrite + arsenopyrite ± pyrrhotite and lack or rarity of sulphates); sulphide textures (particularly framboidal pyrite); lack of chimney structures and rubble mounds; irregular metal or mineral zoning; and the low degree of zone refining compared to Hokuroku ores. The major differences between the provinces are the lack of vent complexes and the presence of Sn–Cu ores in the Iberian pyrite belt. There are also similarities in the geological setting of the two camps: both lie within continental terranes undergoing arc-continent and continent–continent collision, and in each case massive sulphide mineralisation followed ophiolite obduction; the ore deposits are associated with bimodal volcanic rocks derived from MORB and continental crust and marine shales; and mineralisation was locally accompanied or followed by deposition of iron formations.Fluid inclusion data from veins in stockworks from at least six of the Iberian massive sulphide deposits point to sulphide deposition having taken place in basins containing mostly spent saline, ore-forming fluids (brine pools), and it is suggested that most of the major features of the Bathurst deposits can be explained by similar processes. The proposed model is largely independent of ocean sulphate and O2 content, whereas low values of each are requisites for the current, spreading-plume model of sulphide deposition in the Bathurst camp.  相似文献   

13.
Alpha Mound and Beta Mound are two cold‐water coral mounds, located on the Pen Duick Escarpment in the Gulf of Cadiz amidst the El Arraiche mud volcano field where focused fluid seepage occurs. Despite the proximity of Alpha Mound and Beta Mound, both mounds differ in their assemblage of authigenic minerals. Alpha Mound features dolomite, framboidal pyrite and gypsum, whereas Beta Mound contains a barite layer and predominantly euhedral pyrite. The diagenetic alteration of the sedimentary record of both mounds is strongly influenced by biogeochemical processes occurring at shallow sulphate methane transition zones. The combined sedimentological, petrographic and isotopic analyses of early diagenetic features in gravity cores from Alpha Mound and Beta Mound indicate that the contrast in mineral assemblages between these mounds is caused by differences in fluid and methane fluxes. Alpha Mound appears to be affected by strong fluctuations in the fluid flow, causing shifts in redox boundaries, whereas Beta Mound seems to be a less dynamic system. To a large extent, the diagenetic regimes within cold‐water coral mounds on the Pen Duick Escarpment appear to be controlled by fluid and methane fluxes deriving from layers underlying the mounds and forcings like pressure gradients caused by bottom current. However, it also becomes evident that authigenic mineral assemblages are not only very sensitive recorders of the diagenetic history of specific cold‐water coral mounds, but also affect diagenetic processes in turn. Dissolution of aragonite, lithification by precipitation of authigenic minerals and subsequent brecciation of these lithified layers may also exert a control on the advective and diffusive fluid flow within these mounds, providing a feedback mechanism on subsequent diagenetic processes.  相似文献   

14.
The Marl Slate, the English equivalent of the Kupferschiefer, has been studied with particular reference to the relationships between dolomitization and the origin of the metal sulphides. Dolomite occurs as: 1) discontinuous lenses of ferroan dolomicrite, 2) micronodules of finely crystalline dolospar in association with length-slow chalcedony and 3) discrete laminae of ferroan or non-ferroan dolospar. The ferroan dolomicrite has excess CaCO3, and is more abundant in the lower, sapropelic facies of the Marl Slate. It is considered to have formed by the penecontemporaneous alteration of calcium carbonate under hypersaline conditions. Small micronodules (typically about 0.3 mm in diameter) are also more abundant in the sapropelic Marl Slate. These frequently contain cores of length-slow chalcedony (quartzine) fibres and sometimes quartz megacrysts. Textural observations clearly indicate that this silica is of authigenic origin and the dolomite/chalcedony micronodules are interpreted as diagenetic replacements of a calcium sulphate mineral such as anhydrite. The discrete laminae of finely crystalline dolospar are often inter-laminated with calcite in the upper part of the Marl Slate. This dolomite is also calcium rich and represents a replacement, possibly of anhydrite, during a later phase of diagenesis. Metal sulphides occur in two distinct forms: as disseminated framboidal pyrite and as discrete lenses of pyrite, chalcopyrite, galena, sphalerite and rarer sulphides. The framboidal pyrite originated during early diagenesis by reaction of sulphide, produced by reduction of sulphate by organic material and micro-organisms, with iron also released in the reducing environment. The sulphide lenses are often in intimate association with dolospar, length-slow chalcedony and authigenic quartz megacrysts. This indicates that the lenses were produced during diagenesis by the reduction and replacement of calcium sulphate (anhydrite). Various sources, such as co-precipitation with dolomite precursors and the underlying Yellow Sands, may have supplied metals which were mobilized and transported by connate brines as diagenesis progressed.  相似文献   

15.
The Um Samiuki Zn–Cu–Pb–Ag mineralisation, south Eastern Desert, Egypt is hosted by felsic volcanic rocks which form part of the 712-Ma-old, east-west-trending Shadli Volcanic Belt. Two major occurrences of massive sulphides are present at the top of rhyolitic breccia in the Western and Eastern mine areas. In each occurrence, a bornite-bearing zone is overlain by a pyrite-chalcopyrite-bearing zone and underlain by a disseminated, Cu-depleted zone. In the massive sulphide ore, sphalerite, chalcopyrite, pyrite, galena, bornite and tetrahedrite–tennantite are major minerals, whereas arsenopyrite, pyrrhotite, molybdenite and magnetite are accessory phases. Covellite and digenite are common secondary minerals. Bornite, tetrahedrite–tennantite and covellite contain high amounts of silver (averages of 1.97, 1.39 and 1.82 wt% respectively). Based on mineralogical balance calculations, bornite and covellite accommodate 80% of silver in the Um Samiuki deposit. Ag was incorporated in the crystal structure of the early-crystallised copper sulphides and sulphosalts and silver minerals. The temperature, sequential precipitation of the fluids and the structure of the crystallising phases control the distribution of silver. Post-depositional deformation and metamorphic processes caused liberation, remobilisation and redeposition of silver within the massive sulphides.Editorial handling: D. Lentz  相似文献   

16.
Abstract: Through a study, particularly an X-ray photoelectron spectroscopy (XPS or ESCA) analysis, of gold-bearing arsenopyrite and pyrite in Carlin-type gold deposits of Guangxi, China, and hydrothermally synthesized gold-bearing pyrite and marcasite, the authors have found that these minerals contain “invisible gold” whose binding energy is lower than that of native gold (Au°). Therefore they suggest that gold occurs in a negative charge state in these sulphide minerals as it replaces some sulphur and is combined with sulphur with the covalent bond. This paper also preliminarily discusses the possibility of its formation from the chemistry and geochemistry of gold, crystal chemistry of arsenopyrite, pyrite and marcasite and geochemical environment.  相似文献   

17.
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18.
Draa Sfar is a Visean, stratabound, volcanogenic massive sulphide ore deposit hosted by a Hercynian carbonaceous, black shale-rich succession of the Jebilet terrane, Morocco. The ore deposit contains 10 Mt grading 5.3 wt.% Zn, 2 wt.% Pb, and 0.3 wt.% Cu within two main massive sulphides orebodies, Tazakourt (Zn-rich) and Sidi M'Barek (Zn–Cu rich). Pyrrhotite is by far the dominant sulphide (70 to 95% of total sulphides), sphalerite is fairly abundant, chalcopyrite and galena are accessory, pyrite, arsenopyrite and bismuth minerals are rare. Pyrrhotite is monoclinic and mineralogical criteria indicate that it is of primary origin and not formed during metamorphism. Its composition is very homogeneous, close to Fe7S8, and its absolute magnetic susceptibility is 2.10− 3 SI/g. Ar–Ar dating of hydrothermal sericites from a coherent rhyolite flow or dome within the immediate deposit footwall indicates an age of 331.7 ± 7.9 Ma for the Draa Sfar deposit and rhyolite volcanism.The Draa Sfar deposit has undergone a low-grade regional metamorphic event that caused pervasive recrystallization, followed by a ductile–brittle deformation event that has locally imparted a mylonitic texture to the sulphides and, in part, is responsible for the elongated and sheet-like morphology of the sulphide orebodies. Lead isotope data fall into two compositional end-members. The least radiogenic end-member, (206Pb/204Pb = 18.28), is characteristic of the Tazakourt orebody, whereas the more radiogenic end-member (206Pb/204Pb  18.80) is associated with the Sidi M'Barek orebody, giving a mixing trend between the two end-members. Lead isotope compositions at Draa Sfar testify to a significant continental crust source for the base metals, but are different than those of the Hajar and South Iberian Pyrite Belt VMS deposits.The abundance of pyrrhotite versus pyrite in the orebodies is attributed to low fO2 conditions and neither a high temperature nor a low aH2S (below 10− 3) is required. The highly anoxic conditions required to stabilize pyrrhotite over pyrite are consistent with formation of the deposit within a restricted, sediment-starved, anoxic basin characterized by the deposition of carbonaceous, pelagic sediments along the flank of a rhyolitic flow-dome complex that was buried by pelitic sediments. Deposition of sulphides likely occurred at and below the seafloor within anoxic and carbonaceous muds.Draa Sfar and other Moroccan volcanogenic massive sulphide deposits occur in an epicontinental volcanic domain within the outer zone of the Hercynian belt and formed within a sedimentary environment that has a high pelagic component. In spite of the diachronous emplacement between the IPB deposits (late Devonian to Visean) and Moroccan deposits (Dinantian), all were formed around 340 ± 10 Ma following a major phase of the Devonian compression.  相似文献   

19.
The Chouichia and Ain el Bey copper veins that occur in the Eastern Atlas fold belt in northwestern Tunisia, are hosted in Upper Cretaceous-Paleogene sedimentary sequences in a regional transcurrent shear zone. Paragenetic assemblages were formed during four distinct stages all of which are separated by fracturing and brecciation: Stage 1 consists of low temperature siderite (160–180 °C) formation in association with pyrite, including framboidal pyrite and marcasite. Stage 2 includes pseudomorphing of marcasite by As-rich pyrite and arsenopyrite, and formation of chalcopyrite at higher temperatures (200–300 °C) from S-rich, Fe-Cu-bearing fluids; As contents in individual pyrite and arsenopyrite crystals increase markedly in the rims relative to the centers, thus indicating non-equilibrium conditions. Stage 3 involves fracturing and brecciation predating deposition of enargite, luzonite and tennantite at Ain el Bey, and famatinite and tetrahedrite at Chouichia, from As-Sb-Bi-bearing oreforming fluids; tennantite-tetrahedrite series exhibit iron and copper-excess replacements in tetrahedral sites interrelated with Cu-Fe interactions (electron transfer). In Stage 4 fracturing was followed by calcite formation in voids. Comprehensive data was obtained from scanning electron microprobe (SEM) and microprobe chemical analyses of minerals, geothermometry using sulfur isotopes, As contents in arsenopyrite crystals and fluid inclusions in siderite and calcite, support an input of magmatic hydrothermal ore-forming fluids, although contamination by sedimentary sulfur were also identified.  相似文献   

20.
The isotopic composition of Fe was determined in water, Fe-oxides and sulfides from the Tinto and Odiel Basins (South West Spain). As a consequence of sulfide oxidation in mine tailings both rivers are acidic (1.45 < pH < 3.85) and display high concentrations of dissolved Fe (up to 420 mmol l− 1) and sulphates (up to 1190 mmol l− 1).The δ56Fe of pyrite-rich samples from the Rio Tinto and from the Tharsis mine ranged from − 0.56 ± 0.08‰ to + 0.25 ± 0.1‰. δ56Fe values for Fe-oxides precipitates that currently form in the riverbed varied from − 1.98 ± 0.10‰ to 1.57 ± 0.08‰. Comparatively narrower ranges of values (− 0.18 ± 0.08‰ and + 0.21 ± 0.14‰) were observed in their fossil analogues from the Pliocene–Pleistocene and in samples from the Gossan (the oxidized layer that formed through exposure to oxygen of the massive sulfide deposits) (− 0.36 ± 0.12‰ to 0.82 ± 0.07‰). In water, δ56Fe values ranged from − 1.76 ± 0.10‰ to + 0.43 ± 0.05‰.At the source of the Tinto River, fractionation between aqueous Fe(III) and pyrite from the tailings was less than would be expected from a simple pyrite oxidation process. Similarly, the isotopic composition of Gossan oxides and that of pyrite was different from what would be expected from pyrite oxidation. In rivers, the precipitation of Fe-oxides (mainly jarosite and schwertmannite and lesser amounts of goethite) from water containing mainly (more than 99%) Fe(III) with concentrations up to 372 mmol l− 1 causes variable fractionation between the solid and the aqueous phase (− 0.98‰ < Δ56Fesolid–water < 2.25‰). The significant magnitude of the positive fractionation factor observed in several Fe(III) dominated water may be related to the precipitation of Fe(III) sulphates containing phases.  相似文献   

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