On the origin of copper mineralization in the Kupferschiefer: a suIphur isotope study*

Sulphur isotopic compositions of copper and iron sulphides (dispersed and vein mineralization) from the Polish part of the Kupferschiefer were determined and compared with data from the literature. Most of the δ³⁴S values of sulphides range from about -40 to -25%, indicating sulphide precipitation during bacterial sulphate reduction in an open system which gradually chanes into a closed system. Sulphides from veins are usually enriched in ³⁴S compared to finely dispersed mineralization and were probably formed in a more closed system. Copper sulphides are generally a few permil heavier than pyrite. Coupled with detailed microscopical observations the isotope data suggest that the mineralization is either syngenetic or early diagenetic.     

Stratigraphic and petrographic comparison of the Creta and Kupferschiefer copper shale deposits

Stratigraphic and petrographic characteristics of the Creta copper shale deposit in the Flowerpot Shale of southwestern Oklahoma are compared with the betterknown Rudna deposit in the Kupferschiefer of south-western Poland. At Creta, early diagenetic mineralization is indicated by: (1) copper sulfide replacement of large spores and of pyrite, (2) lack of compaction of replaced spores relative to unreplaced spores, (3) enclosure of uncompacted mud and copper sulfides by early matrix gypsum, and (4) location of the ore bed within a thick sequence of fine-grained, low-permeability sediments. This contrasts sharply with evidence of late-diagenetic copper mineralization in the Kupferschiefer at Rudna. Mineralization of copper shales appears to occur over a wide time scale relative to diagenesis of the host sediments.     

The origin of rhythmic sulphide bands from the Permian sandstones (Weissliegendes) in the footwall of the Fore-Sudetic “Kupferschiefer” (Poland)

Rhythmic copper sulphide bands occur in the Weissliegendes sandstones, in the footwall of the Kupferschiefer in the mining district of SW Poland. The δ ³⁴S values of sulphides vary from −39 to — 44‰ (6–7‰ lighter than Kupferschiefer sulphides). The copper sulphides are represented mainly by digenite and chalcocite. According to microprobe results their Pb, Ni, Zn and Ag contents are similar to those in the Kupferschiefer. The bands are assumed to be formed by diffusion of bacterially produced hydrogen sulphide from the Kupferschiefer into the porous volume of the white sandstones containing dissolved copper. The sulphides were precipitated in almost equidistant bands, from top to bottom, probably according to the Ostwald-Prager supersaturation theory. The increase of isotopically heavier sulphur towards the lower levels in the sandstone might be explained by closing of the bacterial sulphate reduction system. Contribution to the IGCP Project No. 254     

Mineralogy and textures of the Lahanos and Kızılkaya massive sulphide deposits,northeastern Turkey,and their similarity to Kuroko ores

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.     

Origin of the Kupferschiefer polymetallic mineralization in Poland

The Kupferschiefer ore series, between the Lower Permian (Rotliegendes) terrestrial redbeds/volcanics and the Upper Permian (Zechstein) marine sequence, is developed as dark-grey organic matter-rich and metal sulphide-containing deposits (reduced zone) and as red-stained organic matter-depleted and iron oxide-bearing sediments (oxidized zone?=?Rote Fäule). The transition zone from oxidized to reduced rocks occurs both vertically and horizontally. This zone is characterized by sparsely disseminated remnant copper sulphides within hematite-bearing sediments, replacements of copper sulphides by iron oxides and covellite, and oxide pseudomorphs after framboidal pyrite. These textural features and copper sulphide replacements after pyrite in reduced sediments imply that the main oxide/sulphide mineralization postdated formation of an early-diagenetic pyrite. Hematite-dominated sediments locally contain enrichments of gold and PGE. The Kupferschiefer mineralization resulted from upward and laterally flowing fluids which oxidized originally pyritiferous organic matter-rich sediments to form hematitic Rote Fäule areas, and which emplaced base and noble metals into reduced sediments. It is argued that long-lived and large-scale lateral fluid flow caused the cross-cutting relationships, expansion of the hematitic alteration front, redistribution of noble metals at the outer parts of oxidized areas, and the location of copper orebodies directly above and around oxidized and gold-bearing areas. The Rote Fäule may be a guide to favourable areas for both the Cu-Ag and new Au-Pt-Pd Kupferschiefer-type deposits.     

Types of copper deposits related to volcanic environment in the Bor district,Yugoslavia

The principal copper deposits associated with Upper Creataceous — Laramian calc-alkaline volcano-plutonic complexes in the Bor district are classified as follows: Volcanogenic massive sulphide deposits are situated in andesitic volcanics, and are composed of pyrite and copper sulphides. Multistage deposition of mineral associations in this area was controlled mainly by secondary boiling of hydrothermal fluids rich in sulphur. Apart from cupriferous pyrite deposits, volcanogenic massive polymetallic deposits, containing a pyritic ZnCu+Pb association, have been found recently in hydrothermally altered dacite- and esite pyroclastics. Porphyry copper deposits are mainly situated in volcanic piles related to subvolcanic intrusions and/or hypabyssal plutons. Some porphyry copper deposits occur in the same structures with massive sulphide orebodies, lying above the porphyry copper system. Conglomerate-type ores consisting of clasts of massive sulphide in an andesitic pile have been discovered recently.     

Syngenetic sulphide minerals in a copper-rich bog

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.     

Hydrothermal pyrite chimneys from the Ballynoe baryte deposit,Silvermines, County Tipperary,Ireland

We report the discovery of pyrite tubes 0.1 to 20mm in diameter in the Ballynoe sedimentary baryte deposit. Well developed tubes comprise concentric layers of pyrite of contrasting crystal sizes 0.05 to 1 mm thick. An outer rim of crystalline baryte 10mm thick commonly coats the tubes where these are not touching. The central canals contain myriad pyrite framboids. These tubes have characteristics in common with the chimney spires found on the East Pacific Rise at 21°N from which metal bearing solutions issue at temperatures of up to 380±30°C. Their presence carries the implication that the baryte deposit was not a distal facies of the Silvermines sedimentary pyritic zinc and lead ore, but was produced from local hydrothermal exhalations, though in a shallower part of the basin than the coeval sulphide deposits which had their own feeders. Some epigenetic mineralization may be awaiting discovery beneath the feeder sites at Ballynoe.     

Geological context,mineralization, and timing of the Juramento sediment-hosted stratiform copper–silver deposit,Salta district,northwestern Argentina

The Juramento deposit in northwestern Argentina exhibits several readily visible general characteristics of sediment-hosted stratiform copper (SSC) mineralization. It consists of fine-grained disseminated base-metal sulfides within marine to lacustrine graybeds (the basal whitish Late Cretaceous Lecho Sandstone and shallow-water carbonates of the overlying Maastrichtian Yacoraite Formation) that overlie a thick sequence of redbeds (the Pirgua Subgroup). The property has been examined and drilled in three successive exploration programs as a possible analog of world-class mineralization in the copperbelts of central Africa and the Kupferschiefer. The present report provides specific field and laboratory results that confirm the classification as SSC-type mineralization. The host graybeds are the basal sandstone and overlying oolitic and stromatolitic units of the Yacoraite Formation, which are shown from textural studies to be carbonaceous and to have initially contained very fine-grained, disseminated, syndiagenetic pyrite. These sediments would have been sufficiently porous and permeable in early diagenetic time to allow an infiltration of metalliferous fluids from the underlying redbeds, resulting in the observed progressive replacement of in situ pyrite by common base-metal sulfides (sphalerite, galena, argentiferous tetrahedrite, and copper-rich sulfides: first chalcopyrite, then bornite, and finally chalcocite). Sulfur isotope analyses indicate that a portion of the sulfur of ore-stage sulfides is isotopically heavier than that of pyrite, possibly due to a contribution from associated gypsum. Ore-stage sulfides are zoned vertically and obliquely through the mineralized zones, from cupriferous sulfides at low stratigraphic levels to lead- and zinc-rich mineralization above, with unreplaced pyrite remaining within upper Yacoraite strata. The zoned sulfides and their replacement textures, the peneconformable configuration of the mineralized zones, and the position of ore-stage mineralization adjacent to a stratigraphically defined redox transition from redbeds upward into graybeds indicate an overprint of copper (and accompanying ore-stage metals) on originally pyritic graybeds. The influx of ore-stage metals, presumably in an oxidized low-temperature brine, terminated with a silicification event that effectively sealed the host carbonates. These observations and the overall genetic interpretation are consistent with the general deposit-scale genetic model for early diagenetic SSC mineralization. The regional geologic context is also consistent with its classification as a SSC deposit: It is hosted by post-oxyatmoversion sediments and was formed in association with evaporites at a low paleolatitude in a major intracontinental rift system.     

A multistage origin for Kupferschiefer mineralization

New Re–Os age determinations on mineralized material from the Polish Kupferschiefer elucidate the timing of mineralization and thus the likely mechanisms of ore deposition. Three mineralization parageneses were analysed: (a) chalcocite as pore space filling in sandstone, (b) disseminated Cu–Mo mineralization in shale, and (c) massive, bedded copper sulphides. The resulting ages fall into two ranges: 245.2 (± 1.6)–264.7 (± 1.8) Ma and 162.3 (± 0.8)–184.3 (± 2.2) Ma. These results substantiate previous age determinations, although no Upper Triassic ages were found in this study. Some of the younger ages for the mineralization could represent alteration and recrystallization of existing sulphides. The results confirm that mineralization took place in several stages, from soon after Kupferschiefer sediment deposition in the Upper Permian and for at least 100 m.y. after, until at least the Cretaceous. The genesis of the mineralization can be explained by the episodic release of hydrothermal fluids from the subsiding adjacent Southern Permian sedimentary basin, although the relative importance of each successive mineralizing ‘event’ for introducing additional metals is as yet unknown.     

Geology and geochemistry of the sediment-hosted Cheshmeh-Konan redbed-type copper deposit,NW Iran

The several-hundred-m-thick Miocene Upper Red Formation in northwestern Iran hosts stratiform and fault-controlled copper mineralization. Copper enrichment in the percent range occurs in dm-thick carbonaceous sandstone and shale units within the clastic redbed sequence and consists of fine-grained disseminated copper sulfides (chalcopyrite, bornite, chalcocite) and supergene alteration minerals (covellite, malachite and azurite). The copper mineralization formed after calcite cementation of the primary rock permeability. Copper sulfides occur mainly as replacement of diagenetic pyrite, which, in turn, replaced organic matter. Electron microprobe analysis on bornite, chalcocite and covellite identifies elevated silver contents in these minerals (up to 0.12, 0.72 and 1.21 wt%, respectively), whereas chalcopyrite and pyrite have only trace amounts of silver (<0.26 and 0.06 wt%, respectively). Microthermometric data on fluid inclusions in authigenic quartz and calcite indicate that the Cu mineralization is related to a diagenetic fluid of moderate-to low temperature (Th = 96–160 °C) but high salinity (25–38 wt% CaCl₂ equiv.). The range of δ³⁴S in pyrite is −41.9 to −16.4‰ (average −31.4‰), where framboidal pyrite shows the most negative values between −41.9 and −31.8‰, and fine-grained pyrite has relatively heavier δ³⁴S values (−29.2 to −16.4‰), consistent with a bacteriogenic derivation of the sulfur. The Cu-sulfides (chalcopyrite, bornite and chalcocite) show slightly heavier values from −14.6 to −9.0‰, and their sulfur sources may be both the precursor pyrite-S and the bacterial reduction of sulfate-bearing basinal brines. Carbonates related to the ore stage show isotopically light values of δ¹³C_V-PDB from −8.2 to −5.1‰ and δ¹⁸O_V-PDB from −10.3 to −7.2‰, indicating a mixed source of oxidation of organic carbon (ca. −20‰) and HCO₃⁻ from seawater/porewater (ca. 0‰). The copper mineralization is mainly controlled by organic matter content and paleopermeability (intragranular space to large fracture patterns), enhanced by feldspar and calcite dissolution. The Cheshmeh-Konan deposit can be classified as a redbed-type sediment-hosted stratiform copper (SSC) deposit.     

The composition of brines in the early diagenetic mineralization of the Permian Kupferschiefer in Germany

The Kupferschiefer is an approximately 0.5 m thick black marly shale of Lower Zechstein age in Germany. If one includes some of its footwall and hanging wall, it contains 300 Mt Cu, 800 Mt Zn and 300 Mt Pb. The regional pattern of metal distribution demonstrates its relationship to Variscan and Permian tectonic structures. Faults and the topographic relief of the basement apparently controlled the uprise and lateral migration of reducing and slightly acid hot brines from deeper crustal levels to supply the metals for the mineralization of the Proto-Kupferschiefer. Deep fluids are mainly richer in Zn than Pb and richer in Pb than Cu. Mixing of such slightly acid fluids with slightly alkaline formation waters (seawater) caused a gradient in pH from about three to eight and in sulfide concentration. Most of the sulfide came from dissolved pyrite which was very light in sulfur isotopes. This gradient controlled the sequential precipitation of bornite, chalcopyrite, (chalcocite), galena and sphalerite, which is observed in a lateral and vertical zoning of these sulfides. The fluids experienced a fractionation of the metals during migration over meter to kilometer distances from the tectonically controlled vents within the unconsolidated Proto-Kupferschiefer. Close to the vents the sulfide deposits attained concentrations up to 2% Zn + Pb + Cu. The migration of the metals over large distances took place in unconsolidated sediment. Thus the major mineralization of the Kupferschiefer has to be classed as an early diagenetic process.     

“Background” δ34S values of Kupferschiefer sulphides in Poland: pyrite-marcasite nodules

Regional background ³⁴S values of pyrite-(marcasite) nodules throughout the Zechstein basin in Poland have been measured to help estimate the proportion of externally derived sulphur in the Kupferschiefer Cu-Ag ores. The ³⁴S values of the 17 FeS₂ nodules measured range widely, from -25.2 to -51.9%., similar to the previously published -28 to -43%. range in disseminated pyrite in the Kupferschiefer. The wide variation cannot be attributed to pyrite versus marcasite mineralogy, amount of contained chalcopyrite or sphalerite, carbonate versus shale host rock, early versus late formation, percent of included calcite, or to size, shape, or texture. There is also no relation with proximity to the centres of copper mineralization in southwestern Poland where sulphides are typically isotopically heavier. The ³⁴S values do, however, vary directly with percent of host-rock fragments included in the nodules. Repeat samples that were washed with acid or hot water show the same wide variation, indicating that contamination by sulphate sulphur in the host rock is not a factor. Neither is organic sulphur because of its small volume. Instead, the sulphur composition may be fundamentally controlled by the formation mechanism of the nodule, whereby ³⁴S-rich sulphide is preferentially concentrated, possibly replacing anhydrite lenses. Alternatively, a network of host rock inclusions might act as a more accessible conduit for later, ³⁴S-rich fluids to infiltrate the nodule and add to earlier, ³⁴S-poor pyrite.In the ore deposits, higher ³⁴S values of ore nodules suggest less indigenous sulphur in limestone than shale lithologies. An isotopic temperature of 61 °C from a chalcopyrite-galena pair agrees with other estimates of <105°C. Higher values in ore nodules/veinlets than in adjacent disseminations, and the calculated ³⁴S_py value from a pyrite-bornite mixture support the idea that metal-bearing ³⁴S-rich fluids penetrated the Kupfer-schiefer through a network of fractures.Contribution to IGCP Project 254 Metalliferous Black Shales     

Two-brine model of the genesis of strata-bound Zechstein deposits (Kupferschiefer type), Poland

These Kupferschiefer deposits were probably formed as a result of a mixing of two brines. The upper cold brine (UCB) is an unmineralized brine rich in Na, Ca, Cl and SO₄, with a pH>7 and originating from evaporites overlying the metal-bearing Zechstein rocks. The lower hot brine (LHB) rich in Mg, K, Cl, SO₄ and CO₃ with a pH<=7 formed in sediments in the central part of the Zechstein basin at a depth of 7,000 m. This brine was subjected to heating and upward convection toward the Fore-Sudetic monocline along the bottom of the Z₁ carbonates. During its migration, it caused albitization, serpentinization and leaching of the primary metal deposits in rocks underlying the Zechstein becoming enriched in heavy metals. The mineralization process, being a result of the mixing of the two brines (UCB and LHB), and catalytic oxidation of the organic matter of the black shale were initiated at shallow depths in the area of the Fore-Sudetic monocline. The boundary of the two brines generally overlapped the strike of the black shale.Parts of the deposit with shale-free host rock suggest that the action of two brines alone was capable of producing economic concentrations of Cu, Pb and Zn. Where the boundary of the two brines overlaps the autooxidation zone (the black shale bottom) and also coincides with radiation of thucholite, concentrations of noble metals result.The characteristic vertical distribution of the triplet CuPbZn from the bottom upward is universal in the Kupferschiefer environment.     

Metal accumulation during and after deposition of the Kupferschiefer from the Sangerhausen Basin,Germany

A densely sampled profile (58 cm in thickness) composed of 13 samples of the Kupferschiefer and overlying Zechstein carbonates from the Sangerhausen Basin, Germany has been analysed by various geochemical and microscopic methods in order to clarify the mechanism of base metal accumulation. In this location, the Kupferschiefer is only slightly influenced by the hematite-bearing, oxidized fluids calledRote Fäule.The determination of facies-dependent parameters along the profile indicates that Kupferschiefer from the Sangerhausen Basin was largely deposited in a marine environment; only at the beginning of Kupferschiefer sedimentation did euxinic conditions prevail. The bottom part of the profile is significantly enriched in trace elements such as Cu, Ph, Zn, As, Co, Ag and U. The Cu concentration amounts to 19.88 wt.%. Post-depositional oxidation of the organic matter is observed only in the transition zone between the Kupferschiefer and the Zechstein conglomerate indicating the influence of ascending, oxidizing brines. Microscopic analyses show that only Fe sulfides form framboidal textures; Cu minerals are present along the total profile preferentially in fractures and as patchy structures composed of chalcocite, chalcopyrite and bornite. In the highly mineralized bottom section, Cu sulfides are associated with pyrobitumen, sparry calcite and arsenopyrite. Results from maturation studies of organic matter suggest that the maximum temperature affecting the Kupferschiefer was approximately 130°C.A 3-step-process of metal accumulation is proposed. During deposition of the sediment, framboidal pyrite and pyrite precursors were precipitated by bacterial SO₄²⁻ reduction (BSR). During diagenesis the pyrite and pyrite precursors were largely replaced by mixed Cu/Fe minerals and by chalcocite (PR). In the section with very high Cu contents (> 8%) reduced sulfur from Fe-sulfides was not sufficient for precipitation of Cu and other trace metals from ascending solutions. In this part of the profile, thermochemical SO₄²⁻ reduction (TSR) occurred after pyrite replacement as indicated by the presence of pyrobitumen and sparry calcite.     

Lewis Ponds, a hybrid carbonate and volcanic-hosted polymetallic massive sulphide deposit, New South Wales, Australia

The Lewis Ponds Zn–Pb–Cu–Ag–Au deposit, located in the eastern Lachlan Fold Belt, central western New South Wales, exhibits the characteristics of both volcanic-hosted massive sulphide and carbonate-hosted replacement deposits. Two stratabound massive to disseminated sulphide zones, Main and Toms, occur in a tightly folded Upper Silurian sequence of marine felsic volcanic and sedimentary rocks. They have a combined indicated resource of 5.7 Mt grading 3.5% Zn, 2.0% Pb, 0.19% Cu, 97 g/t Ag and 1.9 g/t Au. Main Zone is hosted by a thick unit of poorly sorted mixed provenance breccia, limestone-clast breccia and quartz crystal-rich sandstone, whereas Toms Zone occurs in the overlying siltstone. Pretectonic carbonate–chalcopyrite–pyrite and quartz–pyrite stringer veins occur in the footwall porphyritic dacite, south of Toms Zone. Strongly sheared dolomite–chalcopyrite–pyrrhotite veins directly underlie the Toms massive sulphide lens. The mineralized zones consist predominantly of pyrite, sphalerite and galena. Paragenetically early framboidal, dendritic and botryoidal pyrite aggregates and tabular pyrrhotite pseudomorphs of sulphate occur throughout the breccia and sandstone beds that host Main Zone, but are rarely preserved in the annealed massive sulphide in Toms Zone. Main and Toms zones are associated with a semi-conformable hydrothermal alteration envelope, characterized by texturally destructive chlorite-, dolomite- and quartz-rich assemblages. Dolomite, chlorite, quartz, calcite and sulphides have selectively replaced breccia and sandstone beds in the Main Zone host sequence, whereas the underlying porphyritic dacite is weakly sericite altered. Vuggy and botryoidal textures resulted from partial dissolution of the dolomite-altered sedimentary rocks and unimpeded growth of base metal sulphides, carbonate and quartz into open cavities. The intense chlorite-rich alteration assemblage, underlying Toms Zone, grades outward into a weak pervasive sericite–quartz assemblage with distance from the massive sulphide lens. Limestone clasts and hydrothermal dolomite at Lewis Ponds are enriched in light carbon and oxygen isotopes. The dolomite yielded ¹³C_VPDB values of –11 to +1 and ¹⁸O_VSMOW values of 6 to 16. Liquid–vapour fluid inclusions in the dolomite have low salinities (1.4–7.7 equiv. wt% NaCl) and homogenization temperatures (166–232°C for 1,000 m water depth). Dolomitization probably involved fluid mixing or fluid–rock interactions between evolved heated seawater and the limestone-bearing facies, prior to and during mineralization. ³⁴S_VCDT values range from 2.0 to 5.0 in the massive sulphide and 3.9 to 7.4 in the footwall carbonate–chalcopyrite–pyrite stringer veins, indicating that the hydrothermal fluid may have contained mamgatic sulphur and a component of partially reduced seawater. The sulphide mineral assemblages at Lewis Ponds are consistent with moderate to strongly reduced conditions during diagenesis and mineralization. Low temperature dolomitization of limestone-bearing facies in the Main Zone host sequence created secondary porosity and provided a reactive host for fluid-rock interactions. Main Zone formed by lateral fluid flow and sub-seafloor replacement of the poorly sorted breccia and sandstone beds. Base metal sulphide deposition probably resulted from dissolution of dolomite, fluid mixing and increased fluid pH. Pyrite, sphalerite and galena precipitated from a relatively low temperature, 150–250°C hydrothermal fluid. In contrast, Toms Zone was emplaced into fine-grained sediment at or near the seafloor, above a zone of focused up-flowing hydrothermal fluids. Copper-rich assemblages were deposited in the Toms Zone footwall and massive sulphide lenses in Main and Toms zones as the hydrothermal system intensified. During the D₁ deformation, fracture-controlled fluids within the Lewis Ponds fault zone and adjacent footwall volcanic succession remobilized sulphides into syntectonic quartz veins. Lewis Ponds is a rare example of a synvolcanic sub-seafloor hydrothermal system developed within fossiliferous limestone-bearing facies. The close spatial association between limestone, hydrothermal dolomite, massive sulphide and dacite provides a basis for new exploration targets elsewhere in New South Wales.Editorial handling: D. Lentz     

Mercury in Stratabound copper mineralization in the Mammoth area,northwest Queensland

Copper mineralization along the Mount Gordon Fault Zone in northwest Queensland contains sufficient mercury to permit mercury pathfinder techniques to be used for exploration for further deposits in the area. At the Mammoth mine, the No. 1 orebody contains 310–14000 ppb Hg, with the highest contents in “sooty chalcocite” which may be of supergene origin. The B orebody contains 100–4300 ppb Hg, with highest concentrations at the top of the deposit. Other deposits in the Mammoth area contain 10–1600 ppb Hg, with mean mercury contents > 200 ppb in fault-related mineralization.There is a strong positive correlation between mercury and copper, sulfur, silver, arsenic, bismuth, lead, antimony and thallium contents in the deposits which suggests mercury was introduced during the mineralizing process. However, most of the mercury occurs on the surfaces of sulfide minerals, indicating its introduction at a late stage of mineralization.Mercury in the No. 1 orebody is partly of supergene origin whereas primary mineralogy may control mercury distribution in the B orebody. The presence near the Mammoth Fault of a lens of pyrite containing high concentrations of mercury (geometric mean 820 ppb) suggests that the mercury content of pyrite encountered in future exploration programmes in the region might be used to indicate proximity to mineralized fault zones.Gossans derived from copper deposits contain more than five times the amount of mercury in ironstones developed over unmineralized or poorly mineralized fault zones. The mercury contents of iron-rich rocks may be used to discriminate gossans from the numerous fault ironstones in the Mammoth area.     

Paleomagnetism of the Cu�CZn�CPb-bearing Kupferschiefer black shale (Upper Permian) at Sangerhausen, Germany

Syngenetic, diagenetic and epigenetic models have been proposed for the Cu?CZn?CPb Kupferschiefer mineralization at Sangerhausen, Germany. Paleomagnetic and rock magnetic measurements have been made on 205 specimens from mine workings on the margin of the Sangerhausen Syncline. The mineralization is richest in the ??0.5-m-thick Upper Permian (258?±?2?Ma) Kupferschiefer black marly shale (nine sites) and dies out over ??0.2?m in the underlying Weisliegend sandstones (three sites) and overlying Zechstein carbonates (two sites). Except for one site of fault zone gypsum, characteristic remanent magnetization directions were isolated for all 14 sites using alternating field and thermal step demagnetization. These directions provide a negative fold test, indicating that the remanence postdates Jurassic fault block tilting. Rock magnetic measurements show that the Kupferschiefer shale marks a redox front between the oxidized Weissliegend sandstones and non-oxidized Zechstein carbonates. The 14 site directions give a Late Jurassic paleopole at 149?±?3?Ma. It is significantly different from the paleopole reported by E.C. Jowett and others for primary or early diagenetic Rote F?ule alteration that gives an age of 254?±?6?Ma on the current apparent polar wander path and is associated with Kupferschiefer mineralization. We suggest that the Late Jurassic extensional tectonic event that formed the nearby North German Basin also reactivated Variscan basement faults and extended them up through the overlying strata, thereby allowing hydrothermal basement fluids to ascend and epigenetically mineralize the Kupferschiefer shale. The possibility of a 53?±?3?Ma mineralization age is also considered.     

Framboidal pyrite in concretions

Most of the siliceous and carbonaceous concretions found in the black shales of the Aalenian of the Helvetic and Ultrahelvetic nappes in the Swiss Alps contain framboidal pyrite. Some framboids are assembled in polyframboids. The study of these framboids under reflected light and by electronic microanalyzer shows that they are constituted solely of pyrite. These framboids are described and further explanation of their genesis is presented.     

Geology of the High Sulfidation Copper Deposits,Monywa Mine,Myanmar

The 50 km² Monywa copper district lies near the Chindwin River within the northward continuation of the Sunda‐Andaman magmatic arc through western Myanmar. There are four deposits; Sabetaung, Sabetaung South, Kyisintaung, and the much larger Letpadaung 7 km to the southeast. Following exploration drilling which began in 1959, production of copper concentrates from a small open pit started at Sabetaung in 1983. Since 1997, when resources totaled 7 million tonnes contained copper in 2 billion tonnes ore, a heap leach–electro‐winning operation has produced over 400,000 t copper cathode from Sabetaung and Sabetaung South. Ore is hosted by mid‐Miocene andesite or dacite porphyry intrusions, and by early mid‐Miocene sandstone and overlying volcaniclastics including eruptive diatreme facies which the porphyries intrude. District‐wide rhyolite dykes and domes with marginal breccias probably post‐date andesite porphyries in the mine area and lack ore‐grade copper. Host rocks to mineralization are altered to phyllic and advanced argillic hydrothermal assemblages within an outer chlorite zone; hypogene alunite is most abundant at Letpadaung and Kyisintaung. Most mineralization is structurally‐controlled with digenite‐chalcocite in breccia dykes, in steeply dipping NE‐trending sheeted veins, and in stockwork and low‐angle sulfide veins. A high‐grade pipe at Sabetaung grades up to 30% Cu, and much of the ore at Sabetaung South is in a NE‐trending zone of mega‐breccia and stockworked sandstone. The hydrothermal alteration, together with replacement quartz, alunite and barite in breccia dykes and veins, the virtual absence of vein quartz, and the presence of chalcopyrite and bornite only as rare veins and as inclusions within the abundant pyrite, indicate that the deposits are high sulfidation. Regional uplift, resistance to erosion and leaching of the altered and mineralized rocks have resulted in porous limonite‐stained leached caps over 200 m thick forming the Letpadaung and Kyisintaung hills. The barren caps pass abruptly downwards at the water table into the highest grade ore at the top of the supergene enrichment zone, within which copper grade, supergene kaolinite and cubic alunite decrease, and pyrite increases with depth; in contrast, marcasite is mostly shallow. Much of the copper to depths exceeding 200 m below the water table occurs as supergene digenite‐chalcocite and minor covellite. Disseminated chalcocite is mostly near‐surface and hence almost certainly supergene. We infer that during prolonged uplift at all four deposits, oxidation of residual pyrite at the water table generated enough acid to leach all the copper from earlier supergene‐enriched ore; below the water table the resulting acid sulfate solutions partly replaced enargite, covellite, chalcopyrite, bornite and pyrite with supergene chalcocite. Undeformed upward‐fining cross‐bedded conglomerates and sands of the ancestral Chindwin River floodplain overlie the margins of the Sabetaung deposits, form a major aquifer up to 40 m thick, and are a potential host for exotic copper mineralization. A mid‐Miocene pluton is inferred to underlie the Monywa deposits, but the possibility of porphyry‐type mineralization within the district is at best highly speculative.