The multiple sulphur isotope fingerprint of a sub-seafloor oxidative sulphur cycle driven by iron

2020 ◽  
Vol 536 ◽  
pp. 116165 ◽  
Author(s):  
Jiarui Liu ◽  
André Pellerin ◽  
Gareth Izon ◽  
Jiasheng Wang ◽  
Gilad Antler ◽  
...  
2019 ◽  
Vol 157 (7) ◽  
pp. 1112-1120
Author(s):  
Ying Lin ◽  
Nanping Wu ◽  
Da Li ◽  
Hong-Fei Ling

AbstractMultiple sulphur isotope compositions of sedimentary pyrites across the Ediacaran–Cambrian (Ed–C) transition and into the early Cambrian from the Xiaotan section, Yunnan, South China, are presented to explore the evolution of the sulphur cycle. The values of δ34Spy range from 13.5 ‰ to 35.8 ‰, and the values of Δ33Spy range from −0.044 ‰ to 0.063 ‰. The first-order observation of highly positive δ34Spy is consistent with sulphur isotope records from other sedimentary successions (with various degrees of enrichment in 34S), reflecting a common feature in cycling of sulphur among ocean basins. The positive values suggest that pyrite was formed in a depositional setting with limiting availability of sulphate that suppressed the expression of microbial fractionations. The first-order observation of a 10-million-year period of negative Δ33Spy beginning around the Ed–C boundary likely reflects changes in isotopic compositions of sulphur influx to the oceans. Such changes are suggested to be linked to a pulse of preferred weathering of sulphides (with negative Δ33S) relative to sulphate, which may reflect enhanced exposure of pyrites in continental margins due to reorganization of continents at this time. Both δ34Spy and Δ33Spy data imply low seawater sulphate levels, and possibly heterogeneity in sulphate concentrations in the world’s coastal oceans. The predictions about sulphur isotope signatures of evolved seawater (with highly positive δ34S and negative Δ33S) at the Xiaotan section are testable with future measurements of carbonate-associated sulphate (CAS), a proxy of ancient oceanic sulphate that carries information about the operation of sulphur cycling on a global scale.


Nature ◽  
1996 ◽  
Vol 382 (6589) ◽  
pp. 342-343 ◽  
Author(s):  
Kirsten S. Habicht ◽  
Donald E. Canfield

1992 ◽  
Vol 102 (1-4) ◽  
pp. 229-244 ◽  
Author(s):  
Rosa Utrilla ◽  
Catherine Pierre ◽  
Federico Orti ◽  
Juan José Pueyo
Keyword(s):  

2021 ◽  
Author(s):  
Alexey V. Eliseev ◽  
Rustam D. Gizatullin ◽  
Alexandr V. Timazhev

<p>A stationary, computationally efficient  scheme, ChAP-1.0 (Chemistry and Aerosol Processes, version 1.0) for the sulphur cycle in the troposphereis developed. This scheme is envisaged to be implemented into Earth system models of intermediate complexity (EMICs). The scheme accounts for sulphur dioxide emissions into the atmosphere, its deposition to the surface, oxidation to sulphates, and dry and wet deposition of sulphates on the surface.<br>The calculations with the scheme were performed with the anthropogenic emissions of sulphur compounds into the atmosphere for 1850-2000 according to the CMIP5 (Coupled Models Intercomparison Project, phase 5) 'historical' protocol, with the ERA-Interim meteorology, and assuming that natural sources of sulphur into the atmosphere remain unchanged during this period. The model reasonably reproduces characteristics of the tropospheric sulphur cycle known from observations and other simulations (e.g., in the Atmospheric Chemistry and Climate Model Intercomparison Project phase II (ACCMIP) simulations, Copernicus Atmosphere Monitoring Service (CAMS) reanalysis, and the Meteorological Synthesizing Centre–West of the European Monitoring and Evaluation Programme (EMEP MSC-W) data). In particular, in 1980's and 1990's, , when the global anthropogenic emission of sulphur, global atmospheric burdens of SO<sub>2</sub> and SO<sub>4</sub> account, correspondingly, 0.2 TgS and 0.4 TgS. In our scheme, about half of the emitted sulphur dioxide is deposited to the surface and the rest in oxidised into sulphates. The latter mostly removed from the atmosphere by wet deposition. The lifetime of the SO<sub>2</sub> and SO<sub>4</sub> in the atmosphere is, respectively, 1.0±0.1 days and 4.1±0.3 days.<br>Despite its simplicity, our scheme may be successfully used to simulate sulphur/sulphates pollution in the atmosphere at coarse spatial and time scales and an impact of this pollution to direct radiative effect of sulphates on climate, their respective indirect (cloud- and precipitation-related) effects, as well as an impact of sulphur compounds on the terrestrial carbon cycle.</p>


2021 ◽  
pp. jgs2021-027
Author(s):  
Valeria Boyko ◽  
Jürgen Pätzold ◽  
Alexey Kamyshny

High fluxes of iron minerals associated with aeolian dry deposition may result in anomalously high reactive iron content and fast reoxidation of hydrogen sulphide in the sediments that prevents pyrite formation and results in “cryptic” sulphur cycle. In this work, we studied cycling of iron and sulphur in the deep-water (> 800 m water depth) sediments of the Red Sea and its northern extension, Gulf of Aqaba. We found that reactive iron content in the surface sediments of the Gulf of Aqaba and the Red Sea is high, while the content of sulphur-bound iron is very low and decreases with water depth. The presence of pyrite traces and zero-valent sulfur as well as isotopic compositions of sulphate and pyrite, which are consistent with sulphate reduction under substrate-limiting conditions, suggest that cryptic sulfur cycling is likely to be a result of fast reoxidation of hydrogen sulfide rather than microbial sulfate reduction suppression. In the sediments of Shaban Deep, which are overlain with hyper-saline hydrothermal brine, low reactive iron and high organic carbon contents result in a non-cryptic sulphur cycle characterized by preservation of pyrite in the sediments.Thematic collection: This article is part of the Sulfur in the Earth system collection available at: https://www.lyellcollection.org/cc/sulfur-in-the-earth-systemSupplementary material:https://doi.org/10.6084/m9.figshare.c.5508155


Nature ◽  
1983 ◽  
Vol 302 (5906) ◽  
pp. 323-326 ◽  
Author(s):  
Keiko Hattori ◽  
Finley A. Campbell ◽  
H. Roy Krouse

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