Mineralization and Structural Controls of the AB-Bid Carbonate-Hosted Pb-Zn (±Cu) Deposit, Tabas-Posht e Badam Metallogenic Belt, Iran

The Ab-Bid deposit, located in the Tabas-Posht e Badam metallogenic belt (TPMB) in Central Iran, is the largest Pb-Zn (±Cu) deposit in the Behadad-Kuhbanan mining district. Sulfide mineralization in the Ab-Bid deposit formed in Middle Triassic carbonate rocks and contains galena and sphalerite with minor pyrite, chalcopyrite, chalcocite, and barite. Silicification and dolomitization are the main wall-rock alteration styles. Structural and textural observations indicate that the mineralization occurs as fault fills with coarse-textured, brecciated, and replacement sulfides deposited in a bookshelf structure. The Ab-Bid ore minerals precipitated from high temperature (≈180–200 °C) basinal brines within the dolomitized and silicified carbonates. The sulfur isotope values of ore sulfides suggest a predominant thermochemical sulfate reduction (TSR) process, and the sulfur source was probably Triassic-Jurassic seawater sulfate. Given the current evidence, mineralization at Ab-Bid resulted from focusing of heated, over-pressurized brines of modified basinal origin into an active fault system. The association of the sulfide mineralization with intensely altered wall rock represents a typical example of such features in the Mississippi Valley-type (MVT) metallogenic domain of the TPMB. According to the structural data, the critical ore control is a bookshelf structure having mineralized dextral strike-slip faults in the northern part of the Ab-Bid reverse fault, which seems to be part of a sinistral brittle shear zone. Structural relationships also indicate that the strata-bound, fault-controlled Ab-Bid deposit was formed after the Middle Jurassic, and its formation may be related to compressive and deformation stages of the Mid-Cimmerian in the Middle Jurassic to Laramide orogenic cycle in the Late Cretaceous-Tertiary.

Mineral waters and sediments of the ferruginous spring Ulan-Bulak Urulyunguevsky (South-Eastern Transbaikalia, Russia)

The data on the chemical composition and content of balneological components (Fe, H2SiO3, CO2, S2-) for three water samples from the Ulan-Bulak acidic ferruginous spring are presented. For the first time, carbonic water was released in the composition of the spring waters, the origin of which is explained by the ingress of hydrocarbonate water into an acidic medium, followed by dissociation according to the HCO3 - + H+ → H2CO3 → H2O + CO2 scheme. An acidic environment is formed as a result of oxidation of sulfide mineralization, presumably gold-bearing. From secondary minerals at the spring, modern sulfate minerals (gypsum, jarosite), hydromica (illite) were found, ocher sediments are widely developed. Given the uncertain nature of the formation of the spring waters, it is considered worthy of special studies, including an inspection of the presence of sulfide mineralization.

Paleoredox conditions, hydrothermal history, and target vectoring in the Macmillan Pass base-metal district, Yukon, Canada: 2 – Pyrite paragenesis and mineral chemistry

ABSTRACT The MacMillan Pass district in Yukon, Canada, hosts the Tom and Jason clastic sediment-hosted Zn-Pb-Ag-(Ba) deposits. Pyrite-bearing drill core samples were collected from seven drill holes that intersected sulfide mineralization and time-stratigraphically equivalent rocks at varied spatial distances extending up to 3 km away from the deposits to assess the relative timing of pyrite mineralization and the chemistry of pyrite paragenesis. There are four pyrite morphologies: framboids and polyframboids (Py1), subhedral to euhedral inclusion-free crystals (Py2a), silicate inclusion-bearing nodules with serrated edges (Py2b), and euhedral idiomorphic overgrowths on preexisting pyrite morphologies (Py3). These morphological varieties correspond in time from syngenetic to earliest diagenetic growth (Py1), early to late diagenetic growth (Py2a, Py2b), and metamorphic crystallization and/or recrystallization of previous textural varieties (Py3). A representative subset of pyrite grains was analyzed for trace element contents and distributions by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). Analyses by LA-ICP-MS reveal that each textural variety of pyrite has a distinct trace element composition that also varies depending on stratigraphic unit. A suite of clastic sediment-hosted sulfide mineralization-related elements was incorporated into Py2 within sulfide mineralized units at greater abundances than that in unmineralized units (e.g., Zn, As, Pb, Tl, Bi). Lead abundances and Pb/Se and As/Mo values in pyrite are the most robust vectoring tools documented. The timing for clastic sediment-hosted Zn-Pb mineralization was syn and/or post late diagenesis (Py2b). A Ba-enriched horizon was identified in rocks and this is interpreted to be the distal time-stratigraphic equivalent unit to Zn-Pb mineralization. The Ba-enriched horizon contains Py2 with anomalous metal (Tl, Co, Mn, Cd, Zn, Sb) contents and abundant macroscopic baryte, and it is interpreted to represent the distal expression of sulfide mineralization-forming hydrothermal activity. Four genetic models for mineralization are reviewed; however, the only model that is consistent with our whole rock and pyrite geochemistry involves venting of buoyant hydrothermal fluid, mixing with ambient seawater, and remaining or sinking into unconsolidated sediments, with lateral migration up to 2–3 km from the vent source.

Application of molybdenum and thallium isotopes as indicators of paleoredox conditions and genesis of hyper-enriched black shale deposits, Peel River, Yukon, Canada

ABSTRACT Hyper-enriched black shale (HEBS) deposits in northern Yukon, consist of thin (<10 cm), laterally extensive (tens of thousands of km2) stratiform sulfide mineralization layer(s) that are hyper-enriched in Ni, Mo, Zn, platinum group elements, Re, and Au. The genesis of HEBS deposits and the ambient paleoenvironment in which they formed are the subject of vigorous debate. Non-traditional stable isotopes, particularly molybdenum and thallium, are robust paleoredox indicators and we have employed these isotope systems in this study of Yukon HEBS. Systematic sampling and Mo and Tl isotopic analysis of a continuous 200 m stratigraphic section through the Yukon HEBS mineralization and footwall and hanging-wall strata at the Peel River north and south bank showings (spaced five km apart) give δ98Mo –1.24 to –0.53‰ and –8.1 to –5.2 ε-units for the mineralization and –0.70 to 0.60‰ and –6.5 to –2.0 ε-units for the unmineralized strata. These values preclude a hydrothermal origin and strongly suggest that redox processes were responsible for the Yukon HEBS mineralization. The isotopic compositions, together with rare earth element (REE) systematics (REE profile, Y positive anomalies, Ce negative anomalies, and Y/Ho values) and other bulk geochemical redox indicators (Mo, V, Re/Mo, Ni/Co, U/Th, and V/Cr) indicate that the Peel River HEBS mineralization formed because of metal scavenging from seawater in a quiescent, euxinic basinal paleoenvironment.

The Source of Organic Matter and Its Role in Producing Reduced Sulfur for the Giant Sediment-Hosted Jinding Zinc-Lead Deposit, Lanping Basin, Yunnan, Southwest China

The Jinding deposit, located in the northern part of Lanping basin in southwest China, is the second largest Zn-Pb deposit in China and the third largest Mississippi Valley-type deposit identified globally. The deposit consists of several large tabular orebodies within the Jinding dome. Two stages of sulfide mineralization (sphalerite, galena, and pyrite) are identified, which are mainly hosted in the siliciclastic strata of Early Cretaceous and Paleocene age. The early sulfide minerals are mostly fine grained (<100 μm) and disseminated in the host rocks, whereas the late minerals are ty pically coarse grained (up to 1 mm in diameter) and colloform. It is estimated that about 3.17 × 106 m3 of reduced sulfur (H2S) was involved in the sulfide mineralization of the Jinding deposit, although its origin remains equivocal. Here, we investigate the biomarker signatures of organic matter and the mechanism of generation of the H2S. The organic matter in the Jinding deposit occurs mainly as petroleum filling fractures and cavities in the wall rocks and solid bitumen intergrown with sulfides or calcite. Abundant solid bitumen is also found on the surfaces of the carbonate rocks in the Sanhedong Formation as well as in the rock fractures associated with framboidal pyrite. The petrographic characteristics and maturity-related biomarker parameters show that the solid bitumen in the ores has higher thermal maturity than that in the Sanhedong Formation, suggesting that it was generated at different temperatures in the two settings. The source-related parameters suggest that the solid bitumen in the ores and Sanhedong Formation probably both originated in a mixed marine shale and carbonate environment and that the source rocks for the bitumen precursor were late Triassic marine strata. The δ34S values, ranging from –30 to –10‰ for the fine-grained and disseminated sulfide minerals and from –24.50 to –16.27‰ for the solid bitumen in the early (main) mineralization stage, suggest that H2S was generated by microbial sulfate reduction. We propose that this occurred in the Triassic strata prior to or during migration of hydrocarbons to the Jinding dome to form a H2S-enriched paleo-oil reservoir. This hypothesis is supported by the similarity of the δ34S values (–27.62 to –17.38‰) of solid bitumen in the Sanhedong Formation (the source rocks) to that of bitumen in the ores. The late-ore sulfide, however, displays significantly higher δ34S values, ranging from –8 to 0‰. We propose that the H2S of this stage was mainly generated by thermochemical sulfate reduction as a result of the interaction between hydrocarbons, sulfate, and hydrothermal fluid. The hydrocarbons were oxidized into bitumen that has δ34S values from –7.38 to –4.61‰.