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Field to laboratory comparison of metal accumulation on aged microplastics in coastal waters

The Science of The Total Environment 2021 38 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 40 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Minwei Xie, Jun-Lin Huang, Jun-Lin Huang, Qiao‐Guo Tan Zhi Lin, Qiao‐Guo Tan Rong Chen, Rong Chen, Minwei Xie, Minwei Xie, Qiao‐Guo Tan Qiao‐Guo Tan Qiao‐Guo Tan Qiao‐Guo Tan Qiao‐Guo Tan Minwei Xie, Minwei Xie, Qiao‐Guo Tan

Summary

Researchers compared metal accumulation on aged microplastics collected from the field versus laboratory-aged samples in coastal waters, finding differences that highlight the importance of realistic weathering conditions when assessing microplastic-metal interactions.

The ubiquity of microplastics in the environment has attracted much attention on their risks. Though newly produced plastics were considered inert to aqueous metals, a few studies suggest aged microplastics can accumulate metals. Still, knowledge gap exists on the comparability of metal accumulation in field condition and that acquired in controlled laboratory settings. Accordingly, we comparatively assessed the field accumulation and laboratory adsorption of metals on aged microplastics in coastal waters. Microplastics of different polymeric types were aged for 8 weeks at three coastal sites with different contamination levels. Microplastics accumulated metals to substantial concentrations during ageing (median concentrations, μg g: Fe = 950, Mn = 94, Zn = 19, Cu = 2.8, Ni = 1.7, Pb = 1.6, and Cd = 0.005). Adsorption capacity of (aged) microplastics was evaluated in laboratory using a stable isotope tracer method. At environmentally realistic concentrations (μg L, Cd = 1.7, Cu = 4.4, Ni = 5.4, Pb = 0.5, and Zn = 13), the median concentrations of newly adsorbed isotopes on the aged microplastics were 0.01, 1.4, 0.07, 0.56, and 1.1 μg g, respectively, one to two orders of magnitude higher than those adsorbed on pristine microplastics. However, the composition pattern of metals accumulated on aged microplastics differed from the composition of metals newly adsorbed in laboratory: the prior one reflected the contamination status of ageing sites and varied by polymeric types; whereas the laboratory newly adsorbed metals on aged microplastics were uniformly correlated to particulate Fe and Mn concentrations, suggesting Fe and Mn mineral coatings mediated the ensuing metal adsorption. Such discrepancy unveiled the complexity of metal accumulation behavior in the real environment and highlighted that cares should be taken when translating laboratory findings to risk assessment of metal contaminated microplastics in the real environment.

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