College of Environment and Safety Engineering, Fuzhou University, Fuzhou, Fujian, PR China.
School of Oceanography, Shanghai Jiao Tong University, Shanghai, PR China.
Water Res. 2024 Dec 1;267:122512. doi: 10.1016/j.watres.2024.122512. Epub 2024 Sep 24.
The burial of sediment organic matter (SOM) in the estuary and shelf plays an important role in the global carbon cycle. However, it is challenging to determine the source, composition, and burial of SOM in the coastal sea, especially at the molecular level. This was explored in the coastal area outside the largest Yangtze River of China with multiple techniques including elemental and stable isotopic analysis, absorption spectroscopy, fluorescence excitation-emission matrices coupled with parallel factor analysis (EEMs-PARAFAC), and ultra-high resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). The end-member mixing analysis based on δC and δN showed a dominance of marine contribution (up to 70%) at most stations while the terrestrial contribution increased to >55% nearshore in summer at a high fluvial sediment flux. This was consistent with the offshore decreasing humic-like C1 and C2, humification index (HIX), %lignin-like compounds, and %CHO but increasing tryptophan-like C3, biological index (BIX), %protein-like compounds, and %CHOS from EEMs-PARAFAC and FT-ICR-MS analysis. The %clay correlated positively with SOM content, HIX, %lignin-like compounds, O/C, and modified aromaticity index (AI) but correlated negatively with %C3, H/C, and the relative abundance of labile formulas (MLB), while %silt showed contrasting correlations. These results indicated the fine clay sediments adsorbed more humified, aromatic, oxygenated, and terrestrial compounds that were probably more resistant to biodegradation and thus had a higher burial efficiency than those on the silty sediments. Principal component analysis based on SOM indices further revealed different characteristics of SOM in the nearshore, northern offshore, and southern offshore regions, which were probably dependent on the delivery by local current systems. Overall, these findings contributed to unraveling the source and molecular composition of SOM associated with different grain size sediments and local current delivery, which are fundamental for understanding the factors underlying carbon burial in the complex coastal environment.
在河口和陆架埋藏的沉积物有机质(SOM)在全球碳循环中起着重要作用。然而,在沿海海域,特别是在分子水平上,确定 SOM 的来源、组成和埋藏是具有挑战性的。本研究使用包括元素和稳定同位素分析、吸收光谱、荧光激发-发射矩阵结合平行因子分析(EEMs-PARAFAC)和超高分辩率傅里叶变换离子回旋共振质谱(FT-ICR-MS)在内的多种技术,对中国最大长江口以外的沿海地区进行了研究。基于δC 和 δN 的端元混合分析表明,在大多数站位,海洋贡献(高达 70%)占主导地位,而在夏季高河流沉积物通量的近岸地区,陆地贡献增加到>55%。这与离岸逐渐减少的腐殖质样 C1 和 C2、腐殖化指数(HIX)、类木质素化合物的%、类 CHO 化合物的%以及从 EEMs-PARAFAC 和 FT-ICR-MS 分析得出的海源 C3、生物指数(BIX)、类蛋白化合物的%、类 CHOS 的增加一致。%粘土与 SOM 含量、HIX、类木质素化合物、O/C 和改良芳香度指数(AI)呈正相关,与 C3、H/C 和易生物降解公式的相对丰度(MLB)呈负相关,而%粉砂则呈相反的相关性。这些结果表明,细粘土沉积物吸附了更多腐殖质、芳香、含氧和陆地化合物,这些化合物可能更具抗生物降解性,因此比粉砂沉积物具有更高的埋藏效率。基于 SOM 指数的主成分分析进一步揭示了近岸、北部近海和南部近海地区 SOM 的不同特征,这可能依赖于局部流系的输送。总的来说,这些发现有助于揭示与不同粒径沉积物和局部流系输送相关的 SOM 的来源和分子组成,这对于理解复杂沿海环境中碳埋藏的因素具有重要意义。