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Spatial and temporal variability of the surface water pCO 2 and air‐sea CO 2 flux in the equatorial Pacific during 1980–2003: A basin‐scale carbon cycle model
Author(s) -
Wang Xiujun,
Christian James R.,
Murtugudde Ragu,
Busalacchi Antonio J.
Publication year - 2006
Publication title -
journal of geophysical research: oceans
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2005jc002972
Subject(s) - boreal , climatology , oceanography , upwelling , environmental science , sea surface temperature , flux (metallurgy) , pacific decadal oscillation , annual cycle , surface water , atmospheric sciences , carbon cycle , geology , ecosystem , chemistry , paleontology , environmental engineering , biology , ecology , organic chemistry
The surface water pCO 2 data from the past two decades indicate significant seasonal to interannual variability, and the size of the equatorial Pacific CO 2 source is strongly influenced by El Niño and La Niña events. A basin‐scale ocean circulation‐biogeochemistry model is developed to study the carbon cycle in the equatorial Pacific for the period of 1980–2003. The model produces strong spatial and temporal variability in sea minus air pCO 2 (50–170 μatm) and sea‐to‐air CO 2 flux (1–5 mol C m −2 yr −1 ). The magnitude, spatial pattern, and seasonal to interannual variability in the model fields are in general agreement with the observations. Our analyses have demonstrated that dissolved inorganic carbon (DIC) plays a dominant role in determining the interannual variability of the sea surface pCO 2 in the equatorial Pacific. However, sea surface temperature (SST) also has significant influence on the spatial and temporal variability of the sea surface pCO 2 in particular during warm periods. At seasonal timescales, the sea surface pCO 2 is relatively high both in boreal spring and fall, but low in boreal summer in the eastern equatorial Pacific. While the high sea surface pCO 2 in boreal fall is associated with the seasonal upwelling of carbon‐rich water, the high sea surface pCO 2 in boreal spring results mainly from the seasonal warming (e.g., high SST). At interannual timescales, the sea surface pCO 2 is largely associated with the El Niño–Southern Oscillation (ENSO) phenomenon, showing high values during cold ENSO phase but low ones during warm ENSO phase. The overall spatial and temporal variations of the sea surface pCO 2 are dominated by physical processes (e.g., seasonal upwelling and the ENSO cycle). However, biological uptake also plays an important role in modulating the variability of the sea surface pCO 2 , and determining the strength of the equatorial Pacific CO 2 source. On an annual basis, the integrated DIC over the top 50 m of the equatorial Pacific is approximately balanced between the supply due to physical processes (1.47 Pg C) and removal due to the biological activity (0.87 Pg C) and outgassing (0.6 Pg C).

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