Isotope geochemistry of dissolved, precipitated, airborne, and fallout sulfur species associated with springs near Paige Mountain, Norman Range, N.W.T.

1982 ◽  
Vol 19 (7) ◽  
pp. 1395-1407 ◽  
Author(s):  
Robert O. van Everdingen ◽  
M. Asif Shakur ◽  
H. Roy Krouse

δ34S values determined for dissolved sulfate in water discharged by sulfurous springs near Paige Mountain identify gypsum beds in the Lower Devonian Bear Rock Formation as the sulfate source, whereas relatively low δ18O values show that as much as 30% of the sulfate may have gone through a reduction–re-oxidation cycle. Reduced sulfur species in the spring water have negative δ34S values as a result of microbiological isotope fractionation during sulfate reduction; airborne sulfur species (H2S, SO2, H2SO4) and gypsum formed through reaction of H2SO4 fallout with exposed carbonate rocks show similar negative δ34S values. Negative δ18O values for the sulfate radical in H2SO4 fallout and in the alteration product indicate that more than half of the oxygen reacting with airborne H2S is derived from water vapour.

1984 ◽  
Vol 21 (9) ◽  
pp. 997-1007 ◽  
Author(s):  
Robert O. van Everdingen

The Radium (British Columbia) and Miette (Alberta) hot springs occasionally produce "dirty" water that carries varying amounts of solid particles in suspension. Dirty-water events in the period 1959–1983 were caused either by heavy rains (or rapid snowmelt) or by earthquakes with magnitudes of 6.9 or greater, between 740 and 2300 km distant from the springs, in Alaska, Idaho, and Montana. Rainfall-induced events at Miette appear to require at least 34 mm of rain within a 48 h period. Associated decreases in water temperatures and dissolved-solids concentrations and changes in the ionic and isotopic compositions of the spring waters result from mixing of deep thermal water with cooler, less mineralized shallow water. By contrast, the earthquake-triggered events did not have significant thermal or geochemical effects. Suspended solids in the dirty waters represent surficial materials (including vegetation debris) and possibly residues from dissolution of carbonate rocks. At Miette Hot Springs the dirt contains secondary sulfur species (native sulfur and gypsum) derived from the HS− content of the spring water.


2014 ◽  
Vol 2 (12) ◽  
pp. 7293-7308
Author(s):  
Z. Chen ◽  
X. Zhou ◽  
J. Du ◽  
C. Xie ◽  
L. Liu ◽  
...  

Abstract. Hydrogeochemistry of 10 hot springs in the Kangding district was investigated by analyzing cation and anion concentrations of the spring waters. The water samples were collected within 5 days after the Lushan earthquake. The spring waters are classified into 7 chemical types based on the hydrochemical compositions. Comparison with the hydrochemical data before the Lushan earthquake, concentrations of Ca2+, HCO3− and TDS of the waters from the Guanding, Erdaoqiao, Gonghe, Erhaoying, Tianwanhe and Caoke springs evidently increased, which resulted from enhancing interaction between deep-earth fluids and carbonate rocks by the increment of dissolved CO2 in the groundwater. Concentrations of Na+, Cl− and SO42− of the waters from the Guanding, zheduotang, Xinxing and Gonghe springs were decreased, indicating dilution of precipitation water. Concentrations of Na+ and SO42− of the Erhaoying spring water increased, which may be attributed to the more supplement of fluids enriched in sulfur. The results indicate that hydrochemical components of spring water can be used as an effective indicator for earthquakes.


Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1415 ◽  
Author(s):  
Wang ◽  
Wei ◽  
Jiang ◽  
Liu ◽  
Lei ◽  
...  

The fundamental advances in silicon isotope geochemistry have been systematically demonstrated in this work. Firstly, the continuous modifications in analytical approaches and the silicon isotope variations in major reservoirs and geological processes have been briefly introduced. Secondly, the silicon isotope fractionation linked to silicon complexation/coordination and thermodynamic conditions have been extensively stressed, including silicate minerals with variable structures and chemical compositions, silica precipitation and diagenesis, chemical weathering of crustal surface silicate rocks, biological uptake, global oceanic Si cycle, etc. Finally, the relevant geological implications for meteorites and planetary core formation, ore deposits formation, hydrothermal fluids activities, and silicon cycling in hydrosphere have been summarized. Compared to the thermodynamic isotope fractionation of silicon associated with high-temperature processes, that in low-temperature geological processes is much more significant (e.g., chemical weathering, biogenic/non-biogenic precipitation, biological uptake, adsorption, etc.). The equilibrium silicon isotope fractionation during the mantle-core differentiation resulted in the observed heavy isotope composition of the bulk silicate Earth (BSE). The equilibrium fractionation of silicon isotopes among silicate minerals are sensitive to the Si–O bond length, Si coordination numbers (CN), the polymerization degrees of silicate unites, and the electronegativity of cations in minerals. The preferential enrichment of different speciation of dissoluble Si (DSi) (e.g., silicic acid H4SiO40 (H4) and H3SiO4− (H3)) in silica precipitation and diagenesis, and chemical weathering, lead to predominately positive Si isotope signatures in continental surface waters, in which the dynamic fractionation of silicon isotope could be well described by the Rayleigh fractionation model. The role of complexation in biological fractionations of silicon isotopes is more complicated, likely involving several enzymatic processes and active transport proteins. The integrated understanding greatly strengthens the potential of δ30Si proxy for reconstructing the paleo terrestrial and oceanic environments, and exploring the meteorites and planetary core formation, as well as constraining ore deposits and hydrothermal fluid activity.


1979 ◽  
Vol 25 (10) ◽  
pp. 1139-1144 ◽  
Author(s):  
R. G. L. McCready ◽  
G. A. Din ◽  
H. R. Krouse

Growth of Saccharomyces cerevisiae in minimal salts – glucose – SO42− medium with varying concentrations of pantothenate (0–1000 μg/L) produced changes in the cellular lipid content and in the ratio of saturated to unsaturated fatty acids. Substantial differences in SO42−diffusion were also observed with changes in pantothenate concentration. During sulfate reduction, the δ34S value of the evolved sulfide varied with the pantothenate concentration ranging from −31‰ in the absence of pantothenate to 0‰ at 400−1000 μg/L pantothenate. The isotope selectivity is related to the effect of pantothenate concentration on cellular metabolism.


1985 ◽  
Vol 7 ◽  
pp. 94-99 ◽  
Author(s):  
Wang Ping

We report trace element, tritium, and hydrochemical analyses for glaciers in mountain regions of western China, based on about 200 samples collected between 1980 and 1983. Conclusions are drawn about the origin of water vapour contributing to precipitation (local or otherwise) and about the contributions to glacier run-off (meltwater or precipitation), based on the tritium measurements.


2001 ◽  
Vol 67 (2) ◽  
pp. 888-894 ◽  
Author(s):  
Jan Detmers ◽  
Volker Brüchert ◽  
Kirsten S. Habicht ◽  
Jan Kuever

ABSTRACT Batch culture experiments were performed with 32 different sulfate-reducing prokaryotes to explore the diversity in sulfur isotope fractionation during dissimilatory sulfate reduction by pure cultures. The selected strains reflect the phylogenetic and physiologic diversity of presently known sulfate reducers and cover a broad range of natural marine and freshwater habitats. Experimental conditions were designed to achieve optimum growth conditions with respect to electron donors, salinity, temperature, and pH. Under these optimized conditions, experimental fractionation factors ranged from 2.0 to 42.0‰. Salinity, incubation temperature, pH, and phylogeny had no systematic effect on the sulfur isotope fractionation. There was no correlation between isotope fractionation and sulfate reduction rate. The type of dissimilatory bisulfite reductase also had no effect on fractionation. Sulfate reducers that oxidized the carbon source completely to CO2 showed greater fractionations than sulfate reducers that released acetate as the final product of carbon oxidation. Different metabolic pathways and variable regulation of sulfate transport across the cell membrane all potentially affect isotope fractionation. Previous models that explained fractionation only in terms of sulfate reduction rates appear to be oversimplified. The species-specific physiology of each sulfate reducer thus needs to be taken into account to understand the regulation of sulfur isotope fractionation during dissimilatory sulfate reduction.


2013 ◽  
Vol 77 ◽  
pp. 151-162 ◽  
Author(s):  
Yehia H. Dawood ◽  
Mahmoud A. Aref ◽  
Mohammed H. Mandurah ◽  
Ahmed Hakami ◽  
Mohammed Gameil

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