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Seasonal and long‐term dynamics of the upper ocean carbon cycle at Station ALOHA near Hawaii
Author(s) -
Keeling Charles D.,
Brix Holger,
Gruber Nicolas
Publication year - 2004
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 - 10.1029/2004gb002227
Subject(s) - alkalinity , environmental science , carbon cycle , atmosphere (unit) , salinity , flux (metallurgy) , dissolved organic carbon , atmospheric sciences , total inorganic carbon , climate change , oceanography , carbon dioxide , climatology , geology , chemistry , meteorology , ecosystem , ecology , geography , organic chemistry , biology
Long‐term trends and average seasonal variability in the upper ocean carbon cycle are investigated at Station ALOHA, the site of the U.S. JGOFS Hawaii Ocean Time series program (HOT), on the basis of a 14‐year time series (1988–2002) of dissolved inorganic carbon (DIC), alkalinity, and 13 C/ 12 C ratio of DIC data. Salinity‐normalized DIC (sDIC) and computed oceanic p CO 2 show distinct upward trends of 1.2 ± 0.1 μmol kg −1 yr −1 and 2.5 ± 0.1 μatm yr −1 , respectively, while the 13 C/ 12 C isotopic ratio of DIC (expressed as δ 13 C oc ) decreases at a mean rate of −0.027 ± 0.001‰ yr −1 . More than half of the rates of change in sDIC and oceanic p CO 2 , and most of the change in 13 C/ 12 C, are attributed to the uptake of isotopically light anthropogenic CO 2 from the atmosphere. The residual trends appear to be caused mainly by a regional change in the net freshwater budget, perhaps associated with a regime change of the North Pacific climate system near 1997. Computed oceanic p CO 2 is below atmospheric p CO 2 for nearly the entire year, leading to an annual mean surface ocean p CO 2 undersaturation of about 18 μatm, and to an annual uptake of CO 2 from the atmosphere, which we compute to be 1.0 ± 0.1 mol m −2 yr −1 . We estimate that about 30% of this flux relates to the uptake of anthropogenic CO 2 , and the remainder to biologically mediated export of organic carbon. Using a modified version of the diagnostic model of Gruber et al. [1998], constrained by δ 13 C oc , we infer net community production of organic carbon (NCP) to be the dominant process generating the observed seasonal variability in sDIC. The annual integral of NCP, 2.3 ± 0.8 mol m −2 yr −1 , is comparable to previous estimates of biological production in the subtropical North Pacific. Annually integrated fluxes of air‐sea gas exchange and NCP at Station ALOHA are each about two thirds of those computed for the upper ocean near Bermuda using similar methods of estimation [ Gruber et al. , 1998, 2002]. However, the seasonal amplitudes of sDIC and δ 13 C oc near Hawaii are only half as large as near Bermuda, because air‐sea gas exchange and NCP tend to oppose each other near Hawaii, but reinforce each other near Bermuda.