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Quantifying the flux of CaCO 3 and organic carbon from the surface ocean using in situ measurements of O 2 , N 2 , pCO 2 , and pH
Author(s) -
Emerson Steven,
Sabine Christopher,
Cronin Meghan F.,
Feely Richard,
Cullison Gray Sarah E.,
DeGrandpre Mike
Publication year - 2011
Publication title -
global biogeochemical cycles
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.512
H-Index - 187
eISSN - 1944-9224
pISSN - 0886-6236
DOI - 10.1029/2010gb003924
Subject(s) - carbon flux , in situ , flux (metallurgy) , total organic carbon , environmental science , carbon fibers , remote sensing , mineralogy , oceanography , geology , atmospheric sciences , environmental chemistry , chemistry , materials science , meteorology , geography , ecosystem , ecology , organic chemistry , composite number , composite material , biology
Ocean acidification from anthropogenic CO 2 has focused our attention on the importance of understanding the rates and mechanisms of CaCO 3 formation so that changes can be monitored and feedbacks predicted. We present a method for determining the rate of CaCO 3 production using in situ measureme nts of f CO 2 and pH in surface waters of the eastern subarctic Pacific Ocean. These quantities were determined on a surface mooring every 3 h for a period of about 9 months in 2007 at Ocean Station Papa (50°N, 145°W). We use the data in a simple surface ocean, mass balance model of dissolved inorganic carbon (DIC) and alkalinity (Alk) to constrain the CaCO 3 : organic carbon (OC) production ratio to be approximately 0.5. A CaCO 3 production rate of 8 mmol CaCO 3 m −2 d −1 in the summer of 2007 (1.2 mol m −2 yr −1 ) is derived by combining the CaCO 3 : OC ratio with the a net organic carbon production rate (2.5 mol C m −2 yr −1 ) determined from in situ measurements of oxygen and nitrogen gas concentrations measured on the same mooring (Emerson and Stump, 2010). Carbonate chemistry data from a meridional hydrographic section in this area in 2008 indicate that isopycnal surfaces that outcrop in the winter in the subarctic Pacific and deepen southward into the subtropics are a much stronger source for alkalinity than vertical mixing. This pathway has a high enough Alk:DIC ratio to support the CaCO 3 :OC production rate implied by the f CO 2 and pH data.