Oceanic Radiocarbon Between Antarctica and South Africa Along WOCE Section 16 at 30 Degrees E
Author
Leboucher, VivianeOrr, James
Jean-Baptiste, Philippe
Arnold, Maurice
Monfray, Patrick
Tisnérat-Laborde Nadine
Poisson, Alain
Duplessy, Jean-Claude
Issue Date
1999-01-01Keywords
salinityAntarctic Ocean
South Africa
Indian Ocean
Antarctica
Southern Africa
hydrochemistry
carbon cycle
geochemical cycle
Atlantic Ocean
sea water
C 14 C 12
sampling
mass spectra
spectra
Africa
carbon
isotopes
radioactive isotopes
carbon dioxide
stable isotopes
geochemistry
Metadata
Show full item recordCitation
Leboucher, V., Orr, J., Jean-Baptiste, P., Arnold, M., Monfray, P., Tisnérat-Laborde, N., ... & Duplessy, J.-C. (1999). Oceanic radiocarbon between Antarctica and South Africa along WOCE section 16 at 30 degrees E. Radiocarbon, 41(1), 51-73.Journal
RadiocarbonAdditional Links
http://radiocarbon.webhost.uits.arizona.edu/Abstract
Accelerator mass spectrometry (AMS) radiocarbon measurements were made on 120 samples collected between Antarctica and South Africa along 30 degrees E during the WOCE-France CIVA1 campaign in February 1993. Our principal objective was to complement the Southern Ocean's sparse existing data set in order to improve the 14C benchmark used for validating ocean carbon-cycle models, which disagree considerably in this region. Measured 14C is consistent with the theta -S characteristics of CIVA1. Antarctic Intermediate Water (AAIW) forming north of the Polar Front (PF) is rich in 14C, whereas surface waters south of the PF are depleted in 14C. A distinct old 14C signal was found for the contribution of the Pacific Deep Water (PDW) to the return flow of Circumpolar Deep Waters (CDW). Comparison to previous measurements shows a 14C decrease in surface waters, consistent with northward displacement of surface waters, replacement by old deep waters upwelled at the Antarctic Divergence, and atmospheric decline in 14C. Conversely, an increase was found in deeper layers, in the AAIW. Large uncertainties, associated with previous methods for separating natural and bomb 14C when in the Southern Ocean south of 45 degrees S, motivated us to develop a new approach that relies on a simple mixing model and on chlorofluorocarbon (CFC) measurements also taken during CIVA1. This approach leads to inventories for CIVA1 that are equal to or higher than those calculated with previous methods. Differences between old and new methods are especially high south of approximately 55 degrees S, where bomb 14C inventories are relatively modest.Type
Articletext
Language
enISSN
0033-8222ae974a485f413a2113503eed53cd6c53
10.1017/S0033822200019330