Sulfur isotope patterns of iron sulfide and barite nodules in the Upper Cretaceous Chalk of England and their regional significance in the origin of coloured chalks

2016 ◽  
Vol 66 (2) ◽  
pp. 227-256 ◽  
Author(s):  
Christopher V. Jeans ◽  
Alexandra V. Turchyn ◽  
Xu-Fang Hu

AbstractThe relationship between the development of iron sulfide and barite nodules in the Cenomanian Chalk of England and the presence of a red hematitic pigment has been investigated using sulfur isotopes. In southern England where red and pink chalks are absent, iron sulfide nodules are widespread. Two typical large iron sulfide nodules exhibit δ34S ranging from −48.6‰ at their core to −32.6‰ at their outer margins. In eastern England, where red and pink chalks occur in three main bands, there is an antipathetic relationship between the coloured chalks and the occurrence of iron sulfide or barite nodules. Here iron sulfide, or its oxidised remnants, are restricted to two situations: (1) in association with hard grounds that developed originally in chalks that contained the hematite pigment or its postulated precursor FeOH3, or (2) in regional sulfidization zones that cut across the stratigraphy. In the Cenomanian Chalk exposed in the cliffs at Speeton, Yorkshire, pyrite and marcasite (both iron sulfide) nodules range in δ34S from −34.7‰ to +40.0‰. In the lower part of the section δ34S vary from −34.8‰ to +7.8‰, a single barite nodule has δ34S between +26.9‰ and +29.9‰. In the middle part of the section δ34S ranges from +23.8‰ to +40.0‰. In the sulfidization zones that cut across the Cenomanian Chalk of Lincolnshire the iron sulfide nodules are typically heavily weathered but these may contain patches of unoxidised pyrite. In these zones, δ34S ranges from −32.9‰ to +7.9‰. The cross-cutting zones of sulfidization in eastern England are linked to three basement faults – the Flamborough Head Fault Zone, the Caistor Fault and the postulated Wash Line of Jeans (1980) – that have affected the deposition of the Chalk. It is argued that these faults have been both the conduits by which allochthonous fluids – rich in hydrogen sulfide/sulfate, hydrocarbons and possibly charged with sulfate-reducing bacteria – have penetrated the Cenomanian Chalk as the result of movement during the Late Cretaceous or Cenozoic. These invasive fluids are associated with (1) the reduction of the red hematite pigment or its praecursor, (2) the subsequent development of both iron sulfides and barite, and (3) the loss of overpressure in the Cenomanian Chalk and its late diagenetic hardening by anoxic cementation. Evidence is reviewed for the origin of the red hematite pigment of the coloured chalks and for the iron involved in the development of iron sulfides, a hydrothermal or volcanogenic origin is favoured.

1990 ◽  
Vol 218 ◽  
Author(s):  
Dennis A. Bazylinski

AbstractIron sulfide production by bacteria can be classified as extracellular or intracellular. Extracellular iron sulfide production is mediated by anaerobic, dissimilatory sulfate-reducing bacteria which produce sulfide as a product of their respiration. Released sulfide reacts with iron (and other metals) in the extracellular environment producing a variety of iron sulfide minerals including “amorphous iron sulfide”, mackinawite, greigite, pyrrhotite, marcasite, and pyrite. The type of minerals formed is dependent upon pH, Eh, and other physical and chemical factors. Extracellular production of these minerals are examples of biologically-induced mineralization in which mineral formation occurs from chemical and/or physical changes in the surrounding environment by the organism.


2011 ◽  
Vol 368-373 ◽  
pp. 42-47
Author(s):  
Fu Shao Li ◽  
Mao Zhong An ◽  
Dong Xia Duan

Corrosion behaviors of low nickel alloy high strength steel (LNAHSS) was studied by electrochemical impedance spectroscopy and scanning electron microscopy when the coupons of LNAHSS were exposed to the seawater culture media. As the results, LNAHSS was uniformly corroded in the fresh sterilized culture medium in a mode of active dissolution; in the culture medium with sulfate-reducing bacteria (SRB), LNAHSS was protected by the iron sulfides layer to some extent in the early stage of exposure, but severely localized corrosion subsequently occurred resulting from the localized breakdown of iron sulfides layer. So, in risks estimation, special precautions should be taken when LNAHSS serves in the environments containing SRB as the localized area can become the tress raiser.


2013 ◽  
Vol 825 ◽  
pp. 540-543
Author(s):  
Mariana Moreira ◽  
Silvana de Queiroz Silva ◽  
Mônica Cristina Teixeira

The objective of this work was to identify one bacterial consortium adapted to the cultivation in the presence of trivalent arsenic (AsIII). Samples were cultured in flasks containing modified Postgate C liquid medium (selective for sulfate-reducing bacteria, SRB). Six different As concentrations were used: 0.5, 1.0, 2.0, 4.0, 8.0 and 16 mg l-1. The growth of sulfate reducing microorganisms was indirectly observed by the formation of an iron sulfide black precipitate and also by the Eh measures.100 ml aliquots of cultured media were centrifuged and stored at-20°C for DNA extraction by phenol/chloroform method. Universal primers 968F-GC 1392R (Bacteria domain) were used for 16S ribosomal DNA amplification. Microbial diversity was evaluated by denaturing gradient gel electrophoresis (DGGE). After DGGE analysis 7 different bands were selected, cut, sequenced and analyzed using the Ribosomal Database Project Release. Consortium microorganisms identified were: Pantoea agglomerans, Enterobacter sp, Citrobacter sp, Cupriavidusmetallidurans, Ralstonia sp, Burkholderia cepacia and Bacillus sp. Thus the microbial consortium here identified is a good candidate for bioremediation of arsenic contaminated areas and effluents.


1997 ◽  
Vol 36 (1) ◽  
pp. 295-302 ◽  
Author(s):  
Zbigniew Lewandowski ◽  
Wayne Dickinson ◽  
Whonchee Lee

Two mechanisms of microbially influenced corrosion (MIC) are discussed and compared: corrosion modified by the presence of (1) sulfate-reducing bacteria (SRB) and (2) manganese-oxidizing bacteria (MOB). It is demonstrated that the nature of MIC in both cases depends on the nature of inorganic materials precipitated at the metal surface, iron sulfides and manganese oxides. Those materials are electrochemically active and, therefore, modify the electrochemical processes naturally occurring at the metal-solution interface. Some of these modifications may lead to accelerated corrosion.


Geophysics ◽  
1991 ◽  
Vol 56 (6) ◽  
pp. 748-757 ◽  
Author(s):  
M. B. Goldhaber ◽  
R. L. Reynolds

This paper focuses on the association between concentrations of iron disulfide [Formula: see text] minerals in the shallow subsurface and underlying hydrocarbon accumulations. Such [Formula: see text] concentrations are the result of migration of either [Formula: see text] or organic constituents from the underlying hydrocarbons. The [Formula: see text] from reservoirs is produced inorganically from sulfate in the reservoir rocks at high temperature (>90°C) and migrates to shallower beds to react inorganically with iron to form [Formula: see text]. Organic constituents from reservoirs, in contrast, provide nourishment for sulfate reducing bacteria in shallow relatively cool (<90°C) beds. Sandstone in the Ray Point uranium district in Live Oak County, Texas contains abundant [Formula: see text] which formed both from deep‐seated [Formula: see text] and from [Formula: see text] produced in the shallow subsurface by bacteria that utilized organic materials from depth. Deep petroleum reservoirs were physically connected to near‐surface (<100 m) beds containing epigenetic [Formula: see text] by the Oakville fault. Epigenetic iron sulfide formation occurred in at least four episodes over at least five million years. Evidence from the Ray Point district and elsewhere in Texas illustrates that sulfidization reactions have destroyed magnetic iron‐titanium oxide minerals in the vicinity of major growth faults, resulting in a systematic decrease in magnetic susceptibility and magnitude of remanent magnetization in the vicinity of such faults. Growth faults which tap hydrocarbon deposits may be detectable using aeromagnetic methods.


2001 ◽  
Vol 67 (1) ◽  
pp. 51-58 ◽  
Author(s):  
J. M. Benoit ◽  
C. C. Gilmour ◽  
R. P. Mason

ABSTRACT We have previously hypothesized that sulfide inhibits Hg methylation by decreasing its bioavailability to sulfate-reducing bacteria (SRB), the important methylators of Hg in natural sediments. With a view to designing a bioassay to test this hypothesis, we investigated a number of aspects of Hg methylation by the SRBDesulfobulbus propionicus, including (i) the relationship between cell density and methylmercury (MeHg) production, (ii) the time course of Hg methylation relative to growth stage, (iii) changes in the bioavailability of an added inorganic Hg (HgI) spike over time, and (iv) the dependence of methylation on the concentration of dissolved HgI present in the culture. We then tested the effect of sulfide on MeHg production by this microorganism. These experiments demonstrated that under conditions of equal bioavailability, per-cell MeHg production was constant through log-phase culture growth. However, the methylation rate of a new Hg spike dramatically decreased after the first 5 h. This result was seen whether methylation rate was expressed as a fraction of the total added Hg or the filtered HgI concentration, which suggests that Hg bioavailability decreased through both changes in Hg complexation and formation of solid phases. At low sulfide concentration, MeHg production was linearly related to the concentration of filtered HgI. The methylation of filtered HgI decreased about fourfold as sulfide concentration was increased from 10−6 to 10−3 M. This decline is consistent with a decrease in the bioavailability of HgI, possibly due to a decline in the dissolved neutral complex, HgS0.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Huan Yang ◽  
Lanqian Gong ◽  
Hongming Wang ◽  
Chungli Dong ◽  
Junlei Wang ◽  
...  

Abstract Nickel–iron composites are efficient in catalyzing oxygen evolution. Here, we develop a microorganism corrosion approach to construct nickel–iron hydroxides. The anaerobic sulfate-reducing bacteria, using sulfate as the electron acceptor, play a significant role in the formation of iron sulfide decorated nickel–iron hydroxides, which exhibit excellent electrocatalytic performance for oxygen evolution. Experimental and theoretical investigations suggest that the synergistic effect between oxyhydroxides and sulfide species accounts for the high activity. This microorganism corrosion strategy not only provides efficient candidate electrocatalysts but also bridges traditional corrosion engineering and emerging electrochemical energy technologies.


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