Multiple sulfur sources for the volcanic hosted massive sulfides in Betul Belt, Central India: Evidence from the sulfide ore chemistry and sulfur isotope geochemistry

Geochemistry ◽  
2020 ◽  
Vol 80 (4) ◽  
pp. 125632
Author(s):  
Mohammad Atif Raza ◽  
Mohamed Shareef ◽  
Venkata Sri Surya Apla Naidu Badireddi ◽  
Hemraj Suryavanshi ◽  
Srinivasa Rao Baswani ◽  
...  
Minerals ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 588
Author(s):  
Indrani Mukherjee ◽  
Mihir Deb ◽  
Ross R. Large ◽  
Jacqueline Halpin ◽  
Sebastien Meffre ◽  
...  

The Vindhyan Basin in central India preserves a thick (~5 km) sequence of sedimentary and lesser volcanic rocks that provide a valuable archive of a part of the Proterozoic (~1800–900 Ma) in India. Here, we present an analysis of key sedimentary pyrite textures and their trace element and sulfur isotope compositions in the Bijaigarh Shale (1210 ± 52 Ma) in the Vindhyan Supergroup, using reflected light microscopy, LA-ICP-MS and SHRIMP-SI, respectively. A variety of sedimentary pyrite textures (fine-grained disseminated to aggregates, framboids, lags, and possibly microbial pyrite textures) are observed reflecting quiet and strongly anoxic water column conditions punctuated by occasional high-energy events (storm incursions). Key redox sensitive or sensitive to oxidative weathering trace elements (Co, Ni, Zn, Mo, Se) and ratios of (Se/Co, Mo/Co, Zn/Co) measured in sedimentary pyrites from the Bijaigarh Shale are used to infer atmospheric redox conditions during its deposition. Most trace elements are depleted relative to Proterozoic mean values. Sulfur isotope compositions of pyrite, measured using SHRIMP-SI, show an increase in δ34S as we move up stratigraphy with positive δ34S values ranging from 5.9‰ (lower) to 26.08‰ (upper). We propose limited sulphate supply caused the pyrites to incorporate the heavier isotope. Overall, we interpret these low trace element signatures and heavy sulfur isotope compositions to indicate relatively suppressed oxidative weathering on land during the deposition of the Bijaigarh Shale.


2019 ◽  
Vol 104 (9) ◽  
pp. 1256-1272 ◽  
Author(s):  
Indrani Mukherjee ◽  
Ross R. Large ◽  
Stuart Bull ◽  
Daniel G. Gregory ◽  
Aleksandr S. Stepanov ◽  
...  

Abstract Redox-sensitive trace elements and sulfur isotope compositions obtained via in situ analyses of sedimentary pyrites from marine black shales are used to track atmosphere-ocean redox conditions between ∼1730 and ∼1360 Ma in the McArthur Basin, northern Australia. Three black shale formations within the basin (Wollogorang Formation 1730 ± 3 Ma, Barney Creek Formation 1640 ± 3 Ma, and Upper Velkerri Formation 1361 ± 21 Ma) display systematic stratigraphic variations in pyrite trace-element compositions obtained using LA-ICP-MS. The concentrations of several trace elements and their ratios, such as Se, Zn, Se/Co, Ni/Co, Zn/Co, Mo/Co, Se/Bi, Zn/Bi, Ni/Bi, increase from the stratigraphically lower Wollogorang Formation to the Upper Velkerri Formation. Cobalt, Bi, Mo, Cu, and Tl show a consistent decrease in abundance while Ni, As, and Pb show no obvious trends. We interpret these trace element trends as a response to the gradual increase of oxygen in the atmosphere-ocean system from ∼1730 to 1360 Ma. Elements more mobile during erosion under rising atmospheric oxygen show an increase up stratigraphy (e.g., Zn, Se), whereas elements that are less mobile show a decrease (e.g., Co, Bi). We also propose the increase of elemental ratios (Se/Co, Ni/Co, Zn/Co, Mo/Co, Ni/Bi, and Zn/Bi) up stratigraphy are strong indicators of atmospheric oxygenation. Sulfur isotopic compositions of marine pyrite (δ34Spyrite) from these formations, obtained using SHRIMP-SI, are highly variable, with the Wollogorang Formation exhibiting less variation (δ34S = –29.4 to +9.5‰; mean –5.03‰) in comparison to the Barney Creek (δ34S = –13.8 to +41.8‰; mean +19.88‰) and Velkerri Formations (δ34S = –14.2 to +52.8‰; mean +26.9‰). We propose that the shift in mean δ34S to heavier values up-section corresponds to increasing deep water oxygenation from ∼1730 to 1360 Ma. Incursion of oxygenated waters possibly caused a decrease in the areal extent of anoxic areas, at the same time, creating a possibly efficient reducing system. A stronger reducing system caused the δ34S of the sedimentary pyrites to become progressively heavier. Interestingly, heavy δ34S in pyrites overlaps with the increase in the concentration of certain trace elements (and their ratios) in sedimentary pyrites (Se, Zn, Se/Co, Ni/Co, Zn/Co, Mo/Co, Ni/Bi, and Zn/Bi). This study concludes that there was a gradual increase of atmospheric oxygen accompanied by ocean oxygenation through the first ∼400 million years of the Boring Billion (1800–1400 Ma) in the McArthur Basin.


2012 ◽  
Vol 455-456 ◽  
pp. 1345-1349
Author(s):  
Yong Sheng Cheng

The Dachang tin-polymetallic ore deposit is one of the largest Sn ore deposit in the world. For a long time, the Danchi mineralization belt was studied from different perspective, i.e., the mineralization age, the ore source, the deposit model, etc. In fact, the contradistinction of the three mineralization belts has an important macroscopic significance for deepen the genetic mechanism of the Danchi mineralization belt. In the Changpo ore deposit of the west mineralization belt, besides three δ34S values (+4.794, +2.31, +2.6), the δ34S values belong to negative value, yet in the Lamo ore deposit of the middle mineralization belt, most of the δ34S values show positive besides two sulfur isotope sample (δ34S=-0.36, -1.6). But in the Dafulou ore deposit of the east mineralization belt, the δ34S values range from negative value to positive value. So there are only same ore resource partly for the Lamo ore deposit and the Changpo ore deposit. Overall, the ore source of the Dafulou ore deposit is more extensive than other ore deposit, and shares the same ore source with the other ore deposit.


1985 ◽  
Vol 22 (11) ◽  
pp. 1689-1695 ◽  
Author(s):  
Robert O. van Everdingen ◽  
M. Asif Shakur ◽  
Frederick A. Michel

The Paint Pots in Kootenay National Park (British Columbia) appear to derive the Fe, Zn, Pb, and [Formula: see text] contents of their water from sulfide mineralization in Lower and Middle Cambrian carbonates. The Fe, Zn, Ni, and [Formula: see text] contents of groundwater discharging into a tributary of Engineer Creek (Yukon) are likely derived from sulfide mineralization in Devonian or Ordovician black shales exposed in the area. The high Fe and [Formula: see text] contents of a natrojarosite deposit northeast of Fort Norman (Northwest Territories) are probably derived from pyritiferous Cretaceous shales in that area. Isotope analyses of water and of dissolved and precipitated sulfur species from these three sites where acidic, heavy-metal-bearing groundwater is being discharged revealed that between 38 and 74% of the oxygen used in the subsurface oxidation of metal sulfides is supplied by H2O molecules rather than by molecular (dissolved) oxygen. The available data also suggest that lower percentages of water oxygen in the secondary sulfates reflect increasing activity of Thiobacillus ferrooxidans or similar bacteria in the oxidation process.


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