Quantifying microplastic residence times in lakes using mesocosm experiments and transport modelling.

The microplastic residence time in lakes is a key factor controlling its uptake by lake organisms. In this work we have, for the first time, conducted a series of microplastic addition experiments in a 12 × 3 m lake mesocosm and traced its transport through the lake water column. This was combined with a 1D physically based random walk model of microplastic transport. Four experiments were conducted using three microplastic size ranges (1-5, 28-48, and 53-63 µm) over one year during thermal stratification and lake turnover. The results showed that the residence time in the water column largely depended on particle size and lake hydrodynamics, although the smallest particles were poorly represented by the model. Residence times in the mesocosm ranged between ∼1 day for the largest particles to 24 days for the small particles during summer. The modeled residence time were similar to the measured values of the 28-48 µm and 53-63 µm particles, but for the smallest particles residence times were calculated to be >200 d. The discrepancy is likely due to aggregation between the small microplastic particles and natural lake particles, which increases the microplastic settling velocity. Aggregation is favored for the small particles due their large surface area to volume ratio. In contrast, density instabilities in the water column during autumn likely led to turbulent convective mixing and rapid microplastic transport within the water column. This work shows that microplastic transport within lakes is complex and not fully understood, especially for the smallest sizes, and involves interactions between physical, physicochemical and biological processes.

Heteroaggregation of PS microplastic with ferrihydrite leads to rapid removal of microplastic particles from the water column.

Microplastic (MP) particles are ubiquitous in aquatic environments. Therefore, understanding the processes that affect their removal from the water column, such as sedimentation, is critical for evaluating the risk they pose to aquatic ecosystems. We performed sedimentation experiments in which polystyrene (PS) and PS + ferrihydrite, a short-range ordered ferric (oxy)hydroxide, were analyzed in settling columns after 1 day and 1 week of settling time. The presence of ferrihydrite increased sedimentation rates of PS at all pH values studied (pH 3-11). At pH 6 we found that almost all PS particles were removed from the water column after only one day of exposure time. SEM/EDS imaging confirmed heteroaggregation between the PS particles and ferrihydrite. Zeta potential measurements indicated that at acidic pH values the negatively charged PS surface was coated with positively charged ferrihydrite particles leading to charge reversal. Our results demonstrate for the first time that ferric (oxy)hydroxides drive heteroaggregation and subsequent removal of MP from the water column, especially at typical pH values found in natural lake environments. Given their abundance in aquatic systems ferric (oxy)hydroxides need to be regarded as key scavengers of MP.