Molecular
characteristics of natural organic matter (NOM) and their
potential connections to arsenic enrichment processes remain poorly
understood. Here, we examine dissolved organic matter (DOM) in groundwater
and water-soluble organic matter (WSOM) in aquifer sediments being
depth-matched with groundwater samples from a typical arid–semiarid
basin (Hetao Basin, China) hosting high arsenic groundwater. We used
Fourier transform ion cyclotron resonance mass spectrometry to determine
molecular characteristics of DOM and WSOM and evaluate potential roles
of biodegradable compounds in microbially mediated arsenic mobility
at the molecular level. High-arsenic groundwater DOM was generally
enriched in recalcitrant molecules (including lignins and aromatic
structures). Although potential contribution of recalcitrant compounds
to arsenic enrichment cannot be ruled out, preferential degradation
of the labile molecules coupled with reduction of Fe(III) (oxyhydr)oxides
seemed to dominate arsenic mobilization. Both the number and the intensity
of biodegradable compounds (including aliphatic/proteins and carbohydrates)
were higher in WSOM than those in DOM in depth-matched high-arsenic
groundwater (arsenic >0.67 μmol/L or 50 μg/L). Groundwater
arsenic concentration generally increased with the increase in the
number and the intensity of unique biodegradable compounds (especially
N-containing compounds) in WSOM at matched depths. Anoxic incubations
of sediments and deionized water show that more arsenic and Fe(II)
were released from aquifer sediments with greater numbers and intensities
of consumed biodegradable compounds in WSOM (especially N-containing
compounds), with a higher proportion of microbially derived compounds
produced. These observations indicate that the biodegradation of aliphatic/proteins
and carbohydrates (especially CHON formulas) in WSOM fueling the reductive
dissolution of Fe(III) (oxyhydr)oxides predominantly promotes arsenic
release from aquifer solids. Our unique data present a better understanding
of arsenic mobilization shaped by microbial degradation of labile
organic compounds in anoxic aquifers at the molecular level.
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