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Sub-sampling strategies for analysis of small (<20 µm) microplastics in water
Summary
This study tested different methods for measuring very small microplastics (under 20 micrometers) in drinking water and found that analyzing too small a portion of a sample can lead to large errors when estimating total contamination. They determined that researchers need to analyze at least 6-8% of the total filter area to keep errors below 17%. Accurate measurement methods are critical because the smallest microplastics are the most abundant in drinking water and are the most likely to enter human tissues.
Quantification of microplastics (MPs) in drinking water is typically achieved using spectroscopic techniques. However, due to the time-consuming nature of these analyses researchers typically apply sub-sampling strategies whereby particles in small areas of a filter are quantified and subsequently extrapolated to the entire area. This widely applied strategy has not been evaluated in terms of potential extrapolation error despite a wide range of sub-sampling methods having been reported. The current study examined the relationship between sub-sampling and extrapolation accuracy when considering 2-100 µm low-density polyethylene (LDPE), polypropylene (PP), and polystyrene (PS) fragments, with a specific focus on particles <20 µm in size as they are the most abundant and have the potential to exert adverse health impacts. A grid-based random sub-sampling method was developed to serve as a baseline such that extrapolation accuracy could be compared to several previously published methods. Results show that as sub-sampling area increases, error decreases following a power law trend. A minimum sub-sampling threshold was identified (approximately 6-8 % of total area) corresponding to an extrapolation error ranging from 8 to 17 %. Use of a log-normal model to describe particle size distributions was evaluated and found to be applicable to particles >2-5 µm. Findings arising from this study provide insight regarding optimal sub-sampling strategies for the analysis of MP in drinking water.
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