Dynamics of dissolved inorganic carbon in the South China Sea: A modeling study

2020 ◽  
Vol 186 ◽  
pp. 102367
Author(s):  
Chuanjun Du ◽  
Jianping Gan ◽  
Chiwing Rex Hui ◽  
Zhongming Lu ◽  
Xiaozheng Zhao ◽  
...  
Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 624 ◽  
Author(s):  
Xi Xiao ◽  
Qian-Zhi Zhou ◽  
Shao-Ying Fu ◽  
Qian-Yong Liang ◽  
Xiang-Po Xu ◽  
...  

Fe and Mn oxides and (oxy)-hydroxides are the most abundant solid-phase electron acceptors in marine sediments, and dissimilatory Fe/Mn reduction usually links with the anaerobic oxidation of methane (AOM) and organic matter oxidation (OMO) in sediments. In this study, we report the results from subsurface marine sediments in the Dongsha hydrate-bearing area in the South China Sea. The petrological and geochemical signatures show that the Fe/Mn reduction mediated by AOM and OMO might occur in sediments above the sulfate-methane transition zone. X-ray diffraction and scanning electron microscopy analyses of sediments indicate that Fe(III)/Mn(IV)-oxides and authigenic carbonate minerals coexisted in the Fe/Mn reduction zone. The lower δ13C values of dissolved inorganic carbon, coupled with an evident increase in total inorganic carbon contents and a decrease in Ca2+ and Mg2+ concentrations indicate the onset of AOM in this zone, and the greater variation of PO43− and NH4+ concentrations in pore water suggests the higher OMO rates in subsurface sediments. Geochemical and mineralogical analyses suggest that the previously buried Fe(III)/Mn(IV) oxides might be activated and lead to the onset of Fe/Mn reduction induced by AOM and OMO. These findings may extend our understanding of the biogeochemical processes involved in Fe/Mn reduction in continental shelves with abundant methane, organic matter, and terrigenous metal oxides.


2020 ◽  
Vol 125 (4) ◽  
Author(s):  
Ling Ding ◽  
Yuanzhi Qi ◽  
Sen Shan ◽  
Tiantian Ge ◽  
Chunle Luo ◽  
...  

Radiocarbon ◽  
2018 ◽  
Vol 61 (2) ◽  
pp. 461-472 ◽  
Author(s):  
Pan Gao ◽  
Liping Zhou ◽  
Kexin Liu ◽  
Xiaomei Xu

ABSTRACTRadiocarbon (14C) generated by the thermonuclear tests in the late 1950s to early 1960s has been used as a tracer to study atmospheric and oceanic circulations, carbon exchange between different reservoirs, and fossil fuel emissions. Here we report the first measurements of 14C in atmospheric CO2 of maritime air collected over the South China Sea (SCS) during July 2014. We also present 14C of the dissolved inorganic carbon (DIC) in the sea surface water in the same region. Most of the Δ14C values of the atmospheric CO2 vary in the range of 15.6±1.6‰– 22.0±1.6‰, indicating that the central SCS maritime air is well-mixed and consistent with the clean background air in the Northern Hemisphere. The 14C values of the DIC (DI14C) in the surface seawater vary between 28.3±2.5‰ and 40.6±2.7‰, mainly due to the lateral mixing between the SCS and western Pacific. The average surface seawater DI14C is 15.4 ± 5.1‰ higher than that of the maritime air 14CO2. The reversal of the sea–air Δ14C gradient occurred at ∼2000, marking the start of the upper ocean transferring bomb 14C back to the atmosphere in the SCS.


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