Chu Zhao , Guangrui Yang , Lize Meng , Heran Chen , Shuaidong Li , Farong Chen , Zihao Bian , Jiaming Chen , Jian Zhou , Qihao Jiang , Tao Huang , Hao Yang , Changchun Huang
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引用次数: 0
Abstract
Frequent extreme climate events are restructuring riverine carbon cycles dominated by dissolved inorganic carbon (DIC). However, the variability of dissolved organic matter (DOM) induced by rainstorm and its linkage to riverine DIC dynamics remain unclear, limiting an in-depth understanding of carbon transport and fate across the river-ocean continuum. This study employed Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) coupled with stable carbon and water isotope tracing techniques to investigate DOM-DIC interactions in the Yangtze River. Results demonstrated that organic matter constituted a major DIC source, contributing 13.52 ± 1.66% and 23.15 ± 3.27% of total DIC during normal (May) and rainstorm (September) periods in 2021, respectively. Extreme precipitation events (>150 mm·day-1) elevated dissolved organic carbon (DOC) concentration and the biological transformation index (Ibio) of DOM, while reducing molecular mass and double-bond equivalents (DBE) compared to the normal condition. During the rainstorm period, DOC concentration and Ibio values progressively declined downstream with increasing distance from the precipitation core, while molecular mass and DBE increased, contrasting with the spatially homogeneous DOM distribution characteristic of the normal period. Rainstorm enhanced terrestrial organic matter inputs, increasing DOC concentration and enriching low-molecular-weight, highly saturated CHO and CHON compounds. These synergistic effects accelerated DOM biodegradation to organic-sourced DIC (DICoc). Structural equation modeling further confirmed that extreme precipitation primarily promoted DICoc production through stimulated DOM biodegradation rather than photochemical oxidation. Storm events mobilized protein-like compounds from residential wastewater, while elevated water temperatures and nutrient levels collectively enhanced DOM biodegradability. Conversely, rainstorm-induced turbidity plumes suppressed photodegradation of terrestrial aromatic humic substances. Our findings highlight that precipitation-driven DOM loading and molecular transformations significantly accelerate biogeochemical carbon cycling.
期刊介绍:
Water Research, along with its open access companion journal Water Research X, serves as a platform for publishing original research papers covering various aspects of the science and technology related to the anthropogenic water cycle, water quality, and its management worldwide. The audience targeted by the journal comprises biologists, chemical engineers, chemists, civil engineers, environmental engineers, limnologists, and microbiologists. The scope of the journal include:
•Treatment processes for water and wastewaters (municipal, agricultural, industrial, and on-site treatment), including resource recovery and residuals management;
•Urban hydrology including sewer systems, stormwater management, and green infrastructure;
•Drinking water treatment and distribution;
•Potable and non-potable water reuse;
•Sanitation, public health, and risk assessment;
•Anaerobic digestion, solid and hazardous waste management, including source characterization and the effects and control of leachates and gaseous emissions;
•Contaminants (chemical, microbial, anthropogenic particles such as nanoparticles or microplastics) and related water quality sensing, monitoring, fate, and assessment;
•Anthropogenic impacts on inland, tidal, coastal and urban waters, focusing on surface and ground waters, and point and non-point sources of pollution;
•Environmental restoration, linked to surface water, groundwater and groundwater remediation;
•Analysis of the interfaces between sediments and water, and between water and atmosphere, focusing specifically on anthropogenic impacts;
•Mathematical modelling, systems analysis, machine learning, and beneficial use of big data related to the anthropogenic water cycle;
•Socio-economic, policy, and regulations studies.