Determination of the δ13C of dissolved inorganic carbon in water; RSIL lab code 1710

2012 ◽  
pp. i-28 ◽  
Author(s):  
Glenda L. Singleton ◽  
Kinga Revesz ◽  
Tyler B. Coplen
2013 ◽  
Vol 27 (5) ◽  
pp. 635-642 ◽  
Author(s):  
Andres M. Cardenas-Valencia ◽  
Lori R. Adornato ◽  
Ryan J. Bell ◽  
Robert H. Byrne ◽  
R. Timothy Short

1973 ◽  
Vol 30 (10) ◽  
pp. 1441-1445 ◽  
Author(s):  
Michael P. Stainton

A simple, rapid method for determining dissolved inorganic carbon in water is described. A 20-cm3 sample of water is drawn into a 50-cm3 polypropylene syringe and acidified by injection of 1 cm3 of dilute sulphuric acid. Twenty-nine cubic centimeters of helium at atmospheric pressure is injected into the syringe followed by 10 sec of manual agitation to partition CO2 between gas and liquid phase. The gas phase containing 60% of CO2 from the sample is then analyzed by gas chromatography. This method has been used to determine dissolved inorganic and organic carbon in Canadian Shield waters and to determine total carbonates in sediments.


Radiocarbon ◽  
2019 ◽  
Vol 62 (1) ◽  
pp. 13-24 ◽  
Author(s):  
Núria Casacuberta ◽  
Maxi Castrillejo ◽  
Anne-Marie Wefing ◽  
Silvia Bollhalder ◽  
Lukas Wacker

ABSTRACTA new method to extract CO2 in seawater samples for the determination of F14C has been developed in the Laboratory of Ion Beam Physics at ETH Zurich. The setup consists of an automated sampler designed to extract dissolved inorganic carbon (DIC) from 7 samples in a row, by flushing the seawater with He gas to extract CO2. The fully automated method is controlled via a LabVIEW program that runs through all consecutive steps: catalyst preconditioning, CO2 extraction, CO2 trapping, thermal CO2 release from the trap into the reactor and finally the graphitization reaction which is performed simultaneously in the 7 reactors. The method was optimized by introducing a Cu-Ag furnace that was placed between the water and zeolite traps, which resulted in a better and faster graphitization performance (<2 hr) compared to previously used techniques. The method showed to be reproducible with an unprecedented precision of 1.7‰ even though consuming only 50–60 mL of seawater. The high throughput of 21 samples per day allows for coverage of future oceanographic transects with high spatial resolution, thus fostering the use of radiocarbon (14C) as water mass tracer.


2018 ◽  
Vol 90 (7) ◽  
pp. 4677-4685 ◽  
Author(s):  
Laura Freije-Carrelo ◽  
Laura Alonso Sobrado ◽  
Mariella Moldovan ◽  
Jorge Ruiz Encinar ◽  
J. Ignacio García Alonso

The Analyst ◽  
1996 ◽  
Vol 121 (11) ◽  
pp. 1617-1619 ◽  
Author(s):  
Nelson Maniasso ◽  
Sandra Sato ◽  
Maria F. Giné ◽  
Antonio O. Jacintho

2006 ◽  
Vol 63 (1) ◽  
pp. 79-89 ◽  
Author(s):  
Christopher T Solomon ◽  
Peter K Weber ◽  
Joseph J Cech, Jr. ◽  
B Lynn Ingram ◽  
Mark E Conrad ◽  
...  

Otolith stable carbon isotope ratios provide a unique and widely applicable environmental record. Unfortunately, uncertainty regarding the proportion of otolith carbon that derives from metabolized food versus dissolved inorganic carbon (DIC) in the water currently limits utilization of this marker. We manipulated the δ13C of food and ambient DIC in a factorial design with juvenile rainbow trout (Oncorhynchus mykiss). At the activity levels and total metabolic rates characteristic of fish in this study, 17% (±3% standard error, SE) of otolith C was metabolically derived, while >80% was derived from DIC in ambient water. We also estimated isotopic enrichment factors associated with physiological carbon transformations by measuring δ13C of blood and endolymph (which closely tracked otolith δ13C). There was substantial depletion in 13C of blood relative to C sources (εblood–sources = –16.9‰ ± 1.1‰ SE), but substantial enrichment in 13C in otolith relative to blood (εoto–blood = 13.3‰ ± 1.3‰ SE). Net isotopic enrichment between sources and the otolith was therefore slightly negative. Most of the isotopic enrichment between the blood and the otolith was associated with the movement of C from blood to endolymph, while enrichment associated with the precipitation of otolith aragonite from the endolymph was small.


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