Uranium238U/235U Isotope Ratios as Indicators of Reduction: Results from an in situ Biostimulation Experiment at Rifle, Colorado, U.S.A.

2010 ◽  
Vol 44 (15) ◽  
pp. 5927-5933 ◽  
Author(s):  
Charles John Bopp ◽  
Craig C. Lundstrom ◽  
Thomas M. Johnson ◽  
Robert A. Sanford ◽  
Philip E. Long ◽  
...  
Keyword(s):  
Author(s):  
Lei Xu ◽  
Wen Zhang ◽  
Tao Luo ◽  
Jin-Hui Yang ◽  
Zhaochu Hu

High precise and accurate measurements of Fe isotope ratios for fourteen reference materials from the USGS, MPI-DING and CGSG were successfully carried out using a developed analytical technique by fs...


Author(s):  
Andreas Benjamin Kaufmann ◽  
Marina Lazarov ◽  
Stefan Kiefer ◽  
Juraj Majzlan ◽  
Stefan Weyer

Here we present a method for in-situ determination of stable antimony (Sb) isotope compositions by ultraviolet (UV)-femtosecond-laser-ablation-multi-collector-ICP-MS (fs-LA-MC-ICP-MS). Metallic antimony and a number of Sb minerals (stibnite, senarmontite, chalcostibite, tetrahedrite,...


1967 ◽  
Vol 55 (2) ◽  
pp. 263-277 ◽  
Author(s):  
E. Lamb ◽  
S. Mancuso ◽  
S. Dell' Acqua ◽  
N. Wiqvist ◽  
E. Diczfalusy

ABSTRACT Dehydroepiandrosterone sulphate (DHAS) labelled with 3H and dehydroepiandrosterone (DHA) labelled with 14C were simultaneously administered into the arterial supply of four placentas perfused in situ immediately following the removal of the foetus at midpregnancy. From the perfused placentas testosterone (T), androstenedione (A), oestrone (OE1) and 17β-oestradiol (OE2) derived from the metabolism of both DHA and DHAS were isolated in a radiochemically homogeneous form. In addition DHA derived from DHAS was isolated. No labelled 19-hydroxy-androst-4-ene-3,17-dione, or 3β,19-dihydroxy-androst-5-en-17-one was detected. From the perfusates the same steroids were isolated as from the placentas. They contained so small amounts of 3H that their radiochemical homogeneity could be established only on the basis of the 14C label. The 3H/14C ratio of the A isolated from each placenta was higher than that of DHA and OE1 isolated from the same source, indicating a higher contribution of DHAS to A than to DHA or OE1 However, no conjugated or unconjugated intermediates between DHAS and A other than DHA were detected. One possible explanation for the differences in isotope ratios based on the existence of two hypothetical placental compartments, is discussed.


2008 ◽  
Vol 249 (1-2) ◽  
pp. 155-166 ◽  
Author(s):  
Jérôme Chmeleff ◽  
Ingo Horn ◽  
Grit Steinhoefel ◽  
Friedhelm von Blanckenburg

2016 ◽  
Vol 82 (15) ◽  
pp. 4492-4504 ◽  
Author(s):  
Manabu Nishizawa ◽  
Sanae Sakai ◽  
Uta Konno ◽  
Nozomi Nakahara ◽  
Yoshihiro Takaki ◽  
...  

ABSTRACTAmmonia oxidation regulates the balance of reduced and oxidized nitrogen pools in nature. Although ammonia-oxidizing archaea have been recently recognized to often outnumber ammonia-oxidizing bacteria in various environments, the contribution of ammonia-oxidizing archaea is still uncertain due to difficulties in thein situquantification of ammonia oxidation activity. Nitrogen and oxygen isotope ratios of nitrite (δ15NNO2−and δ18ONO2−, respectively) are geochemical tracers for evaluating the sources and thein siturate of nitrite turnover determined from the activities of nitrification and denitrification; however, the isotope ratios of nitrite from archaeal ammonia oxidation have been characterized only for a few marine species. We first report the isotope effects of ammonia oxidation at 70°C by thermophilicThaumarchaeotapopulations composed almost entirely of “CandidatusNitrosocaldus.” The nitrogen isotope effect of ammonia oxidation varied with ambient pH (25‰ to 32‰) and strongly suggests the oxidation of ammonia, not ammonium. The δ18O value of nitrite produced from ammonia oxidation varied with the δ18O value of water in the medium but was lower than the isotopic equilibrium value in water. Because experiments have shown that the half-life of abiotic oxygen isotope exchange between nitrite and water is longer than 33 h at 70°C and pH ≥6.6, the rate of ammonia oxidation by thermophilicThaumarchaeotacould be estimated using δ18ONO2−in geothermal environments, where the biological nitrite turnover is likely faster than 33 h. This study extended the range of application of nitrite isotopes as a geochemical clock of the ammonia oxidation activity to high-temperature environments.IMPORTANCEBecause ammonia oxidation is generally the rate-limiting step in nitrification that regulates the balance of reduced and oxidized nitrogen pools in nature, it is important to understand the biological and environmental factors underlying the regulation of the rate of ammonia oxidation. The discovery of ammonia-oxidizing archaea (AOA) in marine and terrestrial environments has transformed the concept that ammonia oxidation is operated only by bacterial species, suggesting that AOA play a significant role in the global nitrogen cycle. However, the archaeal contribution to ammonia oxidation in the global biosphere is not yet completely understood. This study successfully identified key factors controlling nitrogen and oxygen isotopic ratios of nitrite produced from thermophilicThaumarchaeotaand elucidated the applicability and its limit of nitrite isotopes as a geochemical clock of ammonia oxidation rate in nature. Oxygen isotope analysis in this study also provided new biochemical information on archaeal ammonia oxidation.


2004 ◽  
Vol 207 (3-4) ◽  
pp. 147-169 ◽  
Author(s):  
S Graham ◽  
N Pearson ◽  
S Jackson ◽  
W Griffin ◽  
S.Y O'Reilly
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