Related Experiment Video
Updated: Sep 16, 2025

Elucidating the Metabolism of 2,4-Dibromophenol in Plants
Published on: February 10, 2023
Molecular Insights into Naturally Terrestrial-Derived Halogenated Organic Compounds: Chemodiversity, Speciation, and
Xiangyu Zhu1,2, Enhui Wu1, Kun Wang1,3
1State Key Laboratory of Soil Pollution Control and Safety, Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang 310058, China.
Abstract:
Halogenated organic compounds (HOC) are ubiquitous in soil-water environments and are potentially persistent and toxic. While their occurrence has historically been attributed primarily to anthropogenic sources, growing evidence indicates that substantial natural HOC are stored in terrestrial ecosystems. As an enigmatic pool of soil organic matter, the molecular diversity of soil HOC remains largely unknown. Here, we establish a method to differentiate the speciation and molecular characteristics of soil extractable HOC using (ultra)high-resolution mass spectrometry, optimized through sample extraction solvents and cleanup strategies. Analyzing soil samples from six forest sites across eastern China, we revealed that natural HOC were present in both organic- and water-extractable fractions in all samples, comprising 0.2-14.4% of the total signal abundance. Lipid- and protein-like compounds were more abundant in organic-extractable HOC, while lignin- and lipid-like compounds dominated water-extractable HOC. Furthermore, distinct molecular characteristics were found among the two terrestrial-derived HOC fractions and disinfection byproducts (DBP) commonly detected in aquatic systems, with increasing oxidation and aromaticity, along with decreasing saturation and biolability. We propose a conceptual model describing the divergent molecular properties of natural terrestrial HOC and anthropogenic DBP across the soil-water interface, providing new insights into the different origins and fate of these HOC pools.
More Related Videos
08:22Author Spotlight: A New and Efficient Method for Comprehensive Metabolite Cytotoxicity Assessment of Triazole Pesticides in Plants
Published on: December 22, 2023
05:46Identification of Pharmaceuticals in The Aquatic Environment Using HPLC-ESI-Q-TOF-MS and Elimination of Erythromycin Through Photo-Induced Degradation
Published on: August 1, 2018
Related Concept Videos
Applications of Molecular Taxonomy
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Modern Molecular Taxonomy
Mass Spectrometry: Alkyl Halide Fragmentation
Alkyl Halides
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...