Experimental S isotope fractionation studies between coexisting bismuthinite (Bi2S3) and sulfur (S°)

1982 ◽  
Vol 59 (1) ◽  
pp. 18-20 ◽  
Author(s):  
K. Bente ◽  
H. Nielsen
2012 ◽  
Vol 78 (23) ◽  
pp. 8368-8376 ◽  
Author(s):  
Min Sub Sim ◽  
Shuhei Ono ◽  
Tanja Bosak

ABSTRACTSulfate-reducing microbes utilize sulfate as an electron acceptor and produce sulfide that is depleted in heavy isotopes of sulfur relative to sulfate. Thus, the distribution of sulfur isotopes in sediments can trace microbial sulfate reduction (MSR), and it also has the potential to reflect the physiology of sulfate-reducing microbes. This study investigates the relationship between the availability of iron and reduced nitrogen and the magnitude of S-isotope fractionation during MSR by a marine sulfate-reducing bacterium, DMSS-1, aDesulfovibriospecies, isolated from salt marsh in Cape Cod, MA. Submicromolar levels of iron increase sulfur isotope fractionation by about 50% relative to iron-replete cultures of DMSS-1. Iron-limited cultures also exhibit decreased cytochromec-to-total protein ratios and cell-specific sulfate reduction rates (csSRR), implying changes in the electron transport chain that couples carbon and sulfur metabolisms. When DMSS-1 fixes nitrogen in ammonium-deficient medium, it also produces larger fractionation, but it occurs at faster csSRRs than in the ammonium-replete control cultures. The energy and reducing power required for nitrogen fixation may be responsible for the reverse trend between S-isotope fractionation and csSRR in this case. Iron deficiency and nitrogen fixation by sulfate-reducing microbes may lead to the large observed S-isotope effects in some euxinic basins and various anoxic sediments.


1983 ◽  
Vol 74 (3) ◽  
pp. 165-182 ◽  
Author(s):  
L. G. Love ◽  
M. L. Coleman ◽  
C. D. Curtis

ABSTRACTPyrite textures are described and illustrated and stable S-isotope data are presented from the Alton (Gastrioceras listen) marine horizon of the Westphalian Lower Coal Measures, from sections near Penistone in central northern England, with the object of relating the paragenetic sequence of pyrite formation to the conditions of sediment deposition and diagenesis. The earliest diagenetic pyrite is dispersed as framboidal and related textures. It is followed in the marine shale, coal and ganister by more localised but more intense pyrite deposition and replacement in a variety of textures. Most of this is precompactional in age, but some, together with pyrite in veinlets and cleat, is postcompactional. Marcasite is rare and mainly late. δ34S ratios range between −35·31‰ and +20·39‰. There is a definite trend from lighter values (−1·15 ± 6·47‰) in the marine part of the sequence to much heavier values (+12·73 ± 7·66‰) in the sediment below the coal. This allows the relationship of the earliest pyrite deposition in the coal-peat and ganister to the chemistry of their own depositional fresh water to be seen but then relates the main pyrite deposition to the influx of the marine-water sulphate of the Alton horizon, and shows the penetration of this influence downward into the coal-peat and its seat-bed.


2012 ◽  
Vol 88 ◽  
pp. 183-198 ◽  
Author(s):  
D. Gagnevin ◽  
A.J. Boyce ◽  
C.D. Barrie ◽  
J.F. Menuge ◽  
R.J. Blakeman

2004 ◽  
Vol 21 (3) ◽  
pp. 207-219 ◽  
Author(s):  
Andrea Stögbauer ◽  
Supavadee Koydon ◽  
Zsolt Berner ◽  
Josef Winter ◽  
Doris Stüben

2010 ◽  
Vol 74 (7) ◽  
pp. 2053-2071 ◽  
Author(s):  
Nanping Wu ◽  
James Farquhar ◽  
Harald Strauss ◽  
Sang-Tae Kim ◽  
Donald E. Canfield

2018 ◽  
Author(s):  
Axel Horst ◽  
Magali Bonifacie ◽  
Gérard Bardoux ◽  
Hans-Hermann Richnow

In this study we investigated the isotope fractionation of the abiotic sink (hydrolysis, halide exchange) of methyl halides in water.<br>


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