Frontiers Science Center for Deep Ocean Multispheres and Earth System, Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100, PR China; Laboratory for Marine Ecology and Environmental Science, Qingdao Marine Science and Technology Center, Qingdao 266237, PR China.
First Institute of Oceanography, Ministry of Natural Resources, Qingdao 266061, PR China.
Water Res. 2024 Oct 1;263:122151. doi: 10.1016/j.watres.2024.122151. Epub 2024 Jul 26.
The organic carbon (OC) cycle at the land-ocean interface is an important component of the global carbon budget, yet the processes that control the transfer, transformation, and burial of OC in these regions remain poorly understood. In this work, we examined sedimentary OC (SOC) in short core sediments, dissolved inorganic carbon (DIC), dissolved organic carbon (DOC), and chromophoric dissolved organic matter (CDOM), as well as other solutes in sediment porewaters of the Changjiang Estuary and adjacent East China Sea (ECS) shelf. The main goal of this work is to investigate the variation of the sources and composition of different forms of carbon in estuarine sediments associated with different sedimentary regimes, to further understand the role of sediment porewater in carbon sequestration at the land-ocean interface. Concentrations of Fe and Mn in porewaters of the muddy sediments are much higher than those in the sandy sediments, and SO decreases with depth in the deep sediment layer, indicating the degradation of SOC in mobile muds is mainly driven by suboxic and/or anoxic diagenetic processes (e.g., iron-manganese reduction). The accumulation of DIC in the muddy sediment is higher compared to the sandy sediment, indicating relatively complete SOC remineralization. The DOC in porewaters of the muddy areas is mainly composed of highly degraded and low molecular weight humic-like substances (C1), whereas in the sandy area, porewater DOC is mainly composed of less degraded and high molecular weight protein-like substances (C2 and C3). The average DOC stock (28.5 t/km) in the upper 30 cm sediment porewaters is significantly higher than that of DIC (12.5 t/km) in sandy area, but less in muddy areas (17.0 t/km of DOC vs. 25.4 t/km of DIC). The total DOC stock in sediment porewaters of the sandy area accounted for ∼61 % of DOC stock in water column of the ECS, indicating that the porewater is an important DOC pool in the ECS. However, this DOC pool is rather transient due to its high reactivity and mobility, especially in sandy area. Nevertheless, compared with other marine environments, the carbon stock of DOC (average of 43.8 t/km) in porewaters of stable sedimentary environments is much higher than that of DIC (average of 21.7 t/km). This work further supports the notion that sedimentary regime plays an important role in OC cycling at the land-ocean interface and highlights the significance of sediment porewaters as a vast carbon pool in marine ecosystems.
陆海界面的有机碳(OC)循环是全球碳预算的一个重要组成部分,但控制这些地区 OC 转移、转化和埋藏的过程仍知之甚少。在这项工作中,我们研究了长江口和毗邻东海(ECS)陆架短柱状沉积物中的表层沉积物中的有机碳(SOC)、溶解无机碳(DIC)、溶解有机碳(DOC)和有色溶解有机物质(CDOM)以及其他溶质。这项工作的主要目的是调查与不同沉积环境相关的河口沉积物中不同形式碳的来源和组成的变化,以进一步了解沉积物孔隙水在陆海界面碳封存中的作用。与砂质沉积物相比,泥质沉积物中孔隙水的铁和锰浓度要高得多,并且在深部沉积物中 SO 随着深度的增加而降低,这表明 SOC 的降解主要是由缺氧和/或缺氧成岩作用(例如,铁锰还原)驱动的。与砂质沉积物相比,泥质沉积物中 DIC 的积累量更高,表明 SOC 的还原作用较为完全。泥质区孔隙水中的 DOC 主要由高度降解和低分子量的腐殖质样物质(C1)组成,而在砂质区,孔隙水 DOC 主要由降解程度较低和高分子量的蛋白质样物质(C2 和 C3)组成。在 30cm 上部沉积物孔隙水中,DOC 的平均储量(28.5t/km)明显高于砂质区的 DIC(12.5t/km),但在泥质区则较少(DOC 为 17.0t/km,DIC 为 25.4t/km)。ECS 水柱状 DOC 总量中,砂质区沉积物孔隙水 DOC 占 61%左右,表明孔隙水是 ECS 中一个重要的 DOC 库。然而,由于其高反应性和迁移性,特别是在砂质区,这个 DOC 库是相当短暂的。尽管如此,与其他海洋环境相比,稳定沉积环境中 DOC 储量(平均 43.8t/km)要远高于 DIC 储量(平均 21.7t/km)。这项工作进一步支持了沉积环境在陆海界面 OC 循环中起着重要作用的观点,并强调了沉积环境中孔隙水作为海洋生态系统中巨大碳库的重要性。