Anomalous carbon isotope fractionation between atmospheric CO2 and dissolved inorganic carbon induced by intense photosynthesis

1987 ◽  
Vol 51 (4) ◽  
pp. 895-899 ◽  
Author(s):  
Andrew L Herczeg ◽  
Richard G Fairbanks
2008 ◽  
Vol 22 (14) ◽  
pp. 2410-2423 ◽  
Author(s):  
Daniel H. Doctor ◽  
Carol Kendall ◽  
Stephen D. Sebestyen ◽  
James B. Shanley ◽  
Nobuhito Ohte ◽  
...  

2006 ◽  
Vol 68 (2) ◽  
pp. 142-153 ◽  
Author(s):  
Darren L. Bade ◽  
Michael L. Pace ◽  
Jonathan J. Cole ◽  
Stephen R. Carpenter

Radiocarbon ◽  
2007 ◽  
Vol 49 (1) ◽  
pp. 83-94 ◽  
Author(s):  
I Carmi ◽  
J Kronfeld ◽  
Y Yechieli ◽  
D Yakir ◽  
M Stiller ◽  
...  

Vacuum distillation is shown to be useful for the quantitative extraction of dissolved inorganic carbon (as CO2) and water from sediments of the unsaturated zone in the Coastal Aquifer of Israel. Several tests of vacuum extractions from tap water and sediments are presented, including standard addition, which show that the distillation procedure is quantitative, with minimal or no carbon isotope fractionation. The optimal temperature of the sediment during the extraction was also defined. Examples of vacuum extractions of sediments are shown.


2000 ◽  
Vol 66 (11) ◽  
pp. 4870-4876 ◽  
Author(s):  
D. Hunkeler ◽  
R. Aravena

ABSTRACT Carbon isotope fractionation during aerobic mineralization of 1,2-dichloroethane (1,2-DCA) by Xanthobacter autotrophicusGJ10 was investigated. A strong enrichment of 13C in residual 1,2-DCA was observed, with a mean fractionation factor α ± standard deviation of 0.968 ± 0.0013 to 0.973 ± 0.0015. In addition, a large carbon isotope fractionation between biomass and inorganic carbon occurred. A mechanistic model that links the fractionation factor α to the rate constants of the first catabolic enzyme was developed. Based on the model, it was concluded that the strong enrichment of 13C in 1,2-DCA arises because the first irreversible step of the initial enzymatic transformation of 1,2-DCA consists of an SN2 nucleophilic substitution. SN2 reactions are accompanied by a large kinetic isotope effect. The substantial carbon isotope fractionation between biomass and inorganic carbon could be explained by the kinetic isotope effect associated with the initial 1,2-DCA transformation and by the metabolic pathway of 1,2-DCA degradation. Carbon isotope fractionation during 1,2-DCA mineralization leads to 1,2-DCA, inorganic carbon, and biomass with characteristic carbon isotope compositions, which may be used to trace the process in contaminated environments.


2016 ◽  
Vol 481 ◽  
pp. 9-14 ◽  
Author(s):  
Mirja Hoins ◽  
Tim Eberlein ◽  
Dedmer B. Van de Waal ◽  
Appy Sluijs ◽  
Gert-Jan Reichart ◽  
...  

Geosciences ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 507 ◽  
Author(s):  
Patrick Meister ◽  
Carolina Reyes

Sub-seafloor microbial environments exhibit large carbon-isotope fractionation effects as a result of microbial enzymatic reactions. Isotopically light, dissolved inorganic carbon (DIC) derived from organic carbon is commonly released into the interstitial water due to microbial dissimilatory processes prevailing in the sub-surface biosphere. Much stronger carbon-isotope fractionation occurs, however, during methanogenesis, whereby methane is depleted in 13C and, by mass balance, DIC is enriched in 13C, such that isotopic distributions are predominantly influenced by microbial metabolisms involving methane. Methane metabolisms are essentially mediated through a single enzymatic pathway in both Archaea and Bacteria, the Wood–Ljungdahl (WL) pathway, but it remains unclear where in the pathway carbon-isotope fractionation occurs. While it is generally assumed that fractionation arises from kinetic effects of enzymatic reactions, it has recently been suggested that partial carbon-isotope equilibration occurs within the pathway of anaerobic methane oxidation. Equilibrium fractionation might also occur during methanogenesis, as the isotopic difference between DIC and methane is commonly on the order of 75‰, which is near the thermodynamic equilibrium. The isotopic signature in DIC and methane highly varies in marine porewaters, reflecting the distribution of different microbial metabolisms contributing to DIC. If carbon isotopes are preserved in diagenetic carbonates, they may provide a powerful biosignature for the conditions in the deep biosphere, specifically in proximity to the sulphate–methane transition zone. Large variations in isotopic signatures in diagenetic archives have been found that document dramatic changes in sub-seafloor biosphere activity over geological time scales. We present a brief overview on carbon isotopes, including microbial fractionation mechanisms, transport effects, preservation in diagenetic carbonate archives, and their implications for the past sub-seafloor biosphere and its role in the global carbon cycle. We discuss open questions and future potentials of carbon isotopes as archives to trace the deep biosphere through time.


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