Mobilization and enrichment of geogenic iodine in a floodplain groundwater system: New insights from sources and characterization of dissolved organic matter.

Sci Total Environ

School of Environmental Studies, China University of Geosciences, Wuhan 430078, China; State Environmental Protection Key Laboratory of Source Apportionment and Control of Aquatic Pollution, Ministry of Ecology and Environment, Wuhan 430078, China.

Published: December 2024


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

High iodine groundwater occurs widely in the lower reaches of Yellow River floodplain, which has aroused public concern. The biogeochemical behavior of dissolved organic matter (DOM) plays a crucial role in the mobilizing iodine from aquifer media. In this study, the molecular composition of DOM in groundwater characterized by FT-ICR-MS, and the optical properties of organic matter obtained by combining three-dimensional fluorescence spectroscopy and parallel factor analysis (EEM ⁃ PARAFAC), were used to elucidate the effect of DOM on the migration and enrichment of iodine in groundwater in the eastern Henan Plain, which is located in the lower reaches of Yellow River floodplain, Northern China. The results show that,the total iodine concentration in groundwater in the study area is ranged from 4.68 to 1598 μg/L, and the average value was 216.4 μg/L. High iodine groundwater shows a distribution pattern along the Paleochannels of Yellow River, which is closely related to the richness of organic matter in the buried sediments of the Paleochannels of Yellow River. Organic matter in the sedimentary aquifers plays an important role in regulating the mobilization and enrichment of iodine, and its degradation process is conducive to the release of iodine. DOM components in high iodine groundwater are more homogeneous, more unsaturated, and has more aromatic molecules than those in low iodine groundwater. The activation of organic iodine in groundwater system may be accompanied by the degradation of N+ aliphatic compounds (CHON, CHONSP and CHON) and the formation of oxygen-poor highly unsaturated phenols (CHOSP, CHOP and CHOS) organic compounds. In addition to biodegradation, the adsorption of iron oxide rich in sedimentary aquifers can partially remove the high AI and O/C components of DOM in groundwater and enrich the remaining OPHUP components. The findings provide new insights into the coupling mechanism between iodine release and DOM in aquifers.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.scitotenv.2024.177299DOI Listing

Publication Analysis

Top Keywords

iodine groundwater
24
organic matter
20
yellow river
16
iodine
12
high iodine
12
groundwater
10
mobilization enrichment
8
groundwater system
8
dissolved organic
8
lower reaches
8

Similar Publications

The interaction between dissolved organic matter (DOM) and iodine, as well as the complexation of organoiodine compounds (OICs) with Fe (hydr)oxides, is significantly influenced by their respective molecular characteristics. However, molecular constraints governing the formation and mobility of OICs within aquifer systems remain inadequately understood. Here, we employed ultrahigh-resolution mass spectrometry to investigate the molecular fractionation of organic compounds induced by DOM (humic acid (HA) and fulvic acid (FA)) iodination and by the subsequent formation of OICs complexation with Fe oxides under aquifer conditions.

View Article and Find Full Text PDF

Quenching is essential for terminating chlorination and preserving halogenated disinfection byproducts (X-DBPs) in disinfected waters. However, the effects of quenchers on the chemodiversity and stability of low- and non-volatile X-DBPs are still poorly understood. Four quenchers─sodium sulfite (SS), sodium thiosulfate (STS), ascorbic acid (AA), and 1,3,5-trimethoxybenzene (TMB)─were employed to elucidate their influences on the non-targeted analysis of X-DBPs using Fourier transform ion cyclotron resonance mass spectrometry under negative electrospray ionization mode (ESI(-)-FT-ICR MS).

View Article and Find Full Text PDF

Enrichment mechanisms of selenium in topsoil and subsoil of alluvial and lacustrine basins in Northeast China.

Environ Pollut

August 2025

School of Water Resources and Environment, Key Laboratory of Groundwater Conservation of MWR, and State Key Laboratory of Geomicrobiology and Environmental Changes, China University of Geosciences (Beijing), Beijing, 100083, PR China. Electronic address:

Different hydrodynamic sedimentary conditions may cause significant differences in the enrichment behavior of selenium (Se) in soils with the same provenance. To elucidate basin-scale Se enrichment mechanisms, adjacent Songhua River (alluvial) and Naoli River (lacustrine) Basins with the same bedrocks but differing sedimentary environments were investigated, and 5369 topsoils (0-20 cm depth) and 1380 subsoils (at 1.5 m depth) were collected and analyzed.

View Article and Find Full Text PDF

Coupled biogeochemical processes account for vertical heterogeneity of groundwater iodine in the Hetao Basin.

Water Res

July 2025

MOE Key Laboratory of Groundwater Quality and Health, School of Environmental Studies, China University of Geosciences, Wuhan 430078, China; Key Laboratory of Source Apportionment and Control of Aquatic Pollution, Ministry of Ecology and Environment, Wuhan 430078, China; Hubei Key Laboratory of Yang

Iodine concentration in groundwater exhibits vertical heterogeneity, even within the same aquifer, which is mainly caused by specific biogeochemical processes. However, the microbial contributions to the vertical change of groundwater iodine remain unclear. In this study, we built a monitoring network of 24 wells targeting the depths of 20, 35 and 50 m in a semi-confined aquifer in the Hetao Basin, China and used hydrogeochemistry, metagenomics and metatranscriptomics to elucidate microbial-mediated vertical variations of groundwater iodine.

View Article and Find Full Text PDF

Reductive Dechlorination of 2,3-Dichloroaniline by in an Anaerobic Enrichment Culture.

Environ Sci Technol

July 2025

Department of Civil & Mineral Engineering, University of Toronto, 35 St. George Street, Toronto, Ontario M5S 1A4, Canada.

2,3-dichloroaniline (2,3-DCA) has widespread use in chemical manufacturing and remains a persistent groundwater contaminant. To better understand the pathway and kinetics of its reductive dechlorination, we conducted a laboratory kinetic experiment using an anaerobic enrichment culture dominated by . At an initial field-relevant concentration of 40 mg/L, complete and stoichiometric dechlorination of 2,3-DCA to aniline via 2-chloroaniline (2-CA) was achieved.

View Article and Find Full Text PDF