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Determination of photochemically produced carbon dioxide in seawater
Author(s) -
White Emily M.,
Kieber David J.,
Mopper Kenneth
Publication year - 2008
Publication title -
limnology and oceanography: methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.898
H-Index - 72
ISSN - 1541-5856
DOI - 10.4319/lom.2008.6.441
Subject(s) - carbon dioxide , seawater , total inorganic carbon , detection limit , chemistry , carbon fibers , irradiation , contamination , environmental chemistry , carbonate , carbonic acid , analytical chemistry (journal) , materials science , chromatography , ecology , oceanography , physics , organic chemistry , composite number , nuclear physics , composite material , biology , geology
An analytical system was developed to determine photochemically produced carbon dioxide in marine waters. Our system was designed to measure low levels of carbon dioxide by maintaining a closed system to prevent atmospheric contamination during sample preparation, irradiation, and analysis. To detect low levels of photoproduced carbon dioxide in seawater, background dissolved inorganic carbon (DIC) was removed before irradiation. To strip out DIC, samples were acidified to pH 3.0 (converting DIC to carbon dioxide) and bubbled with low carbon dioxide air. The pH was then readjusted back to the original value, and the resulting low‐DIC seawater samples were transferred pneumatically to air‐tight quartz tubes for irradiation. During analysis, samples were pneumatically transferred to a sample loop, injected, and acidified. Carbon dioxide was then stripped out, dried, and carried to a nondispersive infrared carbon dioxide analyzer. Calibration was done with a series of low concentration aqueous carbonate standards (0.05 to 3 µmol L −1 ). The detection limit, defined as the concentration corresponding to three times the standard deviation of the experimental blank (i.e., DIC‐stripped seawater), was ~60 nmol L −1 . Method precision was largely dependent on the agreement between multiple injections from the same tube (< ±2% relative standard deviation [RSD]) and the reproducibility between different tubes (±3% RSD). This method was used to measure carbon dioxide photoproduction in a variety of waters (e.g., estuarine, lake) including the first direct measurements in marine waters.