微塑料
吸附
海水
生物利用度
环境化学
化学
背景(考古学)
动力学
铜
化学工程
海洋学
有机化学
地质学
生物
工程类
古生物学
物理
量子力学
生物信息学
作者
Ciara Chun Chen,Xiaoshan Zhu,Huo Xu,Fengyuan Chen,Jie Ma,Ke Pan
标识
DOI:10.1021/acs.est.1c04278
摘要
The growing use of plastics has led to microplastics (MPs) being ubiquitously distributed in marine environments. Although previous studies have emphasized MPs as important metal-transport vectors, few have considered the differences between these anthropogenic particles and their coexisting natural counterparts in sequestering metals in seawater. Here, we compared Cu adsorption to pristine and naturally aged MPs (polystyrene and polyethylene) with that to algae particles and sediments and assessed the bioavailability of the adsorbed Cu by a gut juice extraction assay. Adsorption kinetics and isotherms consistently showed that natural particles bound far more Cu to their surfaces than MPs. The rougher surfaces, greater specific surface areas, and lower ζ-potentials of natural particles contributed to their stronger Cu adsorption capacity than pristine or aged MPs. Natural particles also contained more diverse functional groups for binding Cu, with oxygen-containing groups playing a dominant role. Adsorbed Cu on natural particles was less extractable by sipunculan gut juice than that on MPs, indicating their higher Cu affinity. Overall, our study suggests that natural particles outcompete MPs in carrying metals in the water column and transferring them to marine organisms in today's environmental context. This work provides new insights for assessing the risks of MPs in marine environments.
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