TY - JOUR
T1 - Measuring the photochemical production of carbon dioxide from marine dissolved organic matter by pool isotope exchange
AU - Wang, Wei
AU - Johnson, Carl G.
AU - Takeda, Kazuhiko
AU - Zafiriou, Oliver C.
PY - 2009/11/15
Y1 - 2009/11/15
N2 - CO2 is the major known product of solar photolysis of marine dissolved organic matter (DOM). Measuring the rate of this globally significant process is hindered by low rates per unit volume, high background CO2 in seawater, and ubiquitous contamination. Current methods utilize CO 2-free seawater matrices, possibly introducing artifacts. Alternatively, pool isotope exchange (PIE) replaces most of the sample's DI 12C with DI13C at natural pH and temperature, so that 12CO2 from DOM photooxidation elevates 12CO2/13CO2 ratios in irradiated samples compared to dark controls. 12CO2/ 13CO2 ratios are then measured using a modified GC-IRMS. The minimum detectable concentration change (three standard deviations) is 300 nmol DI12C/kg. Methods for minimizing contamination while exchanging, transferring, sealing, and irradiating samples, and for recovering and purifying CO2 are presented. Results from PIE agree within uncertainties with those from CO2-free coastal seawater, suggesting that both methods apply to river-dominated coastal waters. However, photooxidation in the open ocean, which likely dominates the global flux despite lower rates per unit volume, involves DOM that differs from coastal DOM, so that coastal agreement cannot validate open-ocean studies. Major advantages of PIE are use of nearly unperturbed seawater matrices, potential to incubate samples in situ to obtain depth-integrated rates directly, and potential to use larger samples to measure open-ocean waters.
AB - CO2 is the major known product of solar photolysis of marine dissolved organic matter (DOM). Measuring the rate of this globally significant process is hindered by low rates per unit volume, high background CO2 in seawater, and ubiquitous contamination. Current methods utilize CO 2-free seawater matrices, possibly introducing artifacts. Alternatively, pool isotope exchange (PIE) replaces most of the sample's DI 12C with DI13C at natural pH and temperature, so that 12CO2 from DOM photooxidation elevates 12CO2/13CO2 ratios in irradiated samples compared to dark controls. 12CO2/ 13CO2 ratios are then measured using a modified GC-IRMS. The minimum detectable concentration change (three standard deviations) is 300 nmol DI12C/kg. Methods for minimizing contamination while exchanging, transferring, sealing, and irradiating samples, and for recovering and purifying CO2 are presented. Results from PIE agree within uncertainties with those from CO2-free coastal seawater, suggesting that both methods apply to river-dominated coastal waters. However, photooxidation in the open ocean, which likely dominates the global flux despite lower rates per unit volume, involves DOM that differs from coastal DOM, so that coastal agreement cannot validate open-ocean studies. Major advantages of PIE are use of nearly unperturbed seawater matrices, potential to incubate samples in situ to obtain depth-integrated rates directly, and potential to use larger samples to measure open-ocean waters.
UR - https://www.scopus.com/pages/publications/72249105543
U2 - 10.1021/es901543e
DO - 10.1021/es901543e
M3 - Article
C2 - 20028059
AN - SCOPUS:72249105543
SN - 0013-936X
VL - 43
SP - 8604
EP - 8609
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 22
ER -