Alkenone δ13C as a Proxy for PastPCO2 in Surface Waters: Results from the Late Quaternary Angola Current
Alkenone δ13C as a Proxy for PastPCO2 in Surface Waters: Results from the Late Quaternary Angola Current
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烯酮 δ13C 作为地表水中过去 PCO2 的代表:晚第四纪安哥拉洋流的结果
DOI:
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发表时间:
1999
期刊:
影响因子:
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通讯作者:
R. Schneider
中科院分区:
文献类型:
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作者:
N. Andersen;P. Müller;G. Kirst;R. Schneider
Carbon dioxide is one of the most important greenhouse gases which are increasing in atmospheric concentration due to human activities. For using natural CO2 dynamics as a key to understanding the climatic consequences of anthropogenic pCO2 rise, the ocean plays an important role due to its much larger carbon pool compared to the atmosphere. By studying the ratio of stable carbon isotopes in organic matter from marine sediments, it is possible to estimate the partial pressure of CO2 in surface waters during ancient times. The organic compound C37:2 alkenone, whose sole origin is from autotrophic marine algae, was chosen for δ13C analysis and its isotopic composition used to reconstruct past PCO2 levels in the surface layer of the eastern Angola Basin for the last 200,000 years. In addition to the variation of ancient concentrations of dissolved CO2 ([CO2(aq)] = ce), the effect of carbon demand which depends on algal growth rate was considered. Here to, carbon isotopic fractionation of C37:2 alkenones (ep) in core-top sediments from the equatorial and the South Atlantic was calibrated against pre-industrial [CO2(aq)] and phosphate concentrations in surface waters. From these data, a variable b = (25 %-ep)* ce which reflects intracellular carbon demand was calculated. This variable b correlates with the ambient concentration of seawater phosphate and depends on growth rates. The bulk sediment δ15N was used as a proxy parameter for calculating ancient b-values, taking into account that δ15N in core-top sediments is correlated to phosphate concentration in modern surface waters. On this basis, the alkenone δ13C record of GeoB 1016-3 documents a permanent oceanic source for atmospheric carbon dioxide during the last 200,000 years. As a consequence of using δ15N derived b-values instead of b = constant, the Angola Basin appears to have been an even stronger CO2 source during glacial periods than at present. Qualitatively similar results were reported by Jasper et al. (1994) for the central Equatorial Pacific. These observations suggest that enhanced productivity of low-latitude upwelling areas during glacial periods is not responsible for the lower CO2 content of the glacial atmosphere.