Heavy metals trigger distinct molecular transformations in microplastic-versus natural-derived dissolved organic matter

IF 14.3 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Xianbao Zhong , Kaiying Zhao , Mengyuan Wu , Yaohui Zhang , Chiyue Ma , Hexiang Liu , Bokun Chang , Xiaohui Lian , Yujing Li , Zixuan Huang , Lang Zhu , Ming Zhang , Chi Zhang , Yajun Yang , Jialong Lv
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引用次数: 0

Abstract

Dissolved organic matter (DOM) is a key determinant of heavy metal fate in aquatic environments, influencing their mobility, toxicity, and bioavailability. Derived from natural sources such as soil and vegetation decomposition, natural DOM (N-DOM) typically features humic-like substances with abundant oxygen-containing functional groups that stabilize heavy metals through complexation. However, microplastic-derived DOM (MP-DOM), increasingly prevalent due to plastic degradation, may interact differently with heavy metals, potentially exacerbating environmental risks amid rising plastic pollution. Yet, how heavy metals drive molecular transformations in MP-DOM versus N-DOM remains unclear, hindering accurate pollution assessments. Here, we compare interactions between N-DOM and MP-DOM with cadmium, chromium (Cr), copper, and lead from both fluorescence and molecular perspectives. Our results show that N-DOM, dominated by humic-like substances (46.0–57.3 %), lignin-like (55.0–64.9 %), and tannin-like (10.1–17.6 %) compounds, forms more stable heavy metal complexes via carboxyl, phenolic hydroxyl, and ether groups than MP-DOM. By contrast, MP-DOM—enriched in protein/phenolic-like substances (13.8–24.0 %), condensed aromatic (12.1–28.5 %), and protein/aliphatic-like (8.6–12.4 %) compounds—yields less stable complexes and is highly susceptible to Cr-induced oxidation. Mass-difference network analysis and density functional theory calculations further reveal that both DOM types undergo heavy-metal-triggered decarboxylation and dealkylation, but N-DOM retains complex structures, whereas MP-DOM degrades into smaller, hazardous molecules such as phenol and benzene. This study underscores the potential for heavy metals to exacerbate the ecological risks associated with the transformation of MP-DOM, providing crucial insights to inform global risk assessment and management strategies in contaminated waters where plastic and metal pollution co-occur.

Abstract Image

重金属在微塑料中引发不同的分子转化,而不是天然衍生的溶解有机物
溶解有机物(DOM)是水生环境中重金属命运的关键决定因素,影响其流动性、毒性和生物利用度。天然DOM (N-DOM)来源于土壤和植被分解等天然来源,通常具有腐殖质样物质,含有丰富的含氧官能团,通过络合作用稳定重金属。然而,由于塑料降解,微塑料衍生的DOM (MP-DOM)越来越普遍,可能与重金属发生不同的相互作用,可能加剧塑料污染日益严重的环境风险。然而,重金属如何驱动MP-DOM与N-DOM的分子转化仍不清楚,这阻碍了准确的污染评估。在这里,我们从荧光和分子角度比较了N-DOM和MP-DOM与镉、铬、铜和铅的相互作用。结果表明,N-DOM以腐植酸类物质(46.0 ~ 57.3%)、木质素类物质(55.0 ~ 64.9%)和单宁类物质(10.1 ~ 17.6%)为主,通过羧基、酚羟基和醚基形成比MP-DOM更稳定的重金属配合物。相比之下,mp - dom -富含蛋白质/酚类物质(13.8 - 24.0%),凝聚芳香(12.1 - 28.5%)和蛋白质/脂肪类(8.6 - 12.4%)化合物-产生不稳定的复合物,并且对cr诱导的氧化非常敏感。质量差网络分析和密度泛函数理论计算进一步表明,两种DOM类型都经历了重金属触发的脱羧和脱烷基反应,但N-DOM保留了复杂的结构,而MP-DOM降解为更小的有害分子,如苯酚和苯。该研究强调了重金属加剧与MP-DOM转化相关的生态风险的可能性,为塑料和金属污染共存的受污染水域的全球风险评估和管理策略提供了重要见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
20.40
自引率
6.30%
发文量
11
审稿时长
18 days
期刊介绍: Environmental Science & Ecotechnology (ESE) is an international, open-access journal publishing original research in environmental science, engineering, ecotechnology, and related fields. Authors publishing in ESE can immediately, permanently, and freely share their work. They have license options and retain copyright. Published by Elsevier, ESE is co-organized by the Chinese Society for Environmental Sciences, Harbin Institute of Technology, and the Chinese Research Academy of Environmental Sciences, under the supervision of the China Association for Science and Technology.
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