Abiotic Long-Term Simulation of Microplastic Weathering Pathways under Different Aqueous Conditions.

Microplastics (MPs) are one of the most abundant and widespread anthropogenic pollutants worldwide. In addition to the global spread and threats of plastic to native species by carrying toxic substances, its slow degradation rate and resulting long retention time in the environment constitute a problem that is still poorly understood. In this study, five of the most manufactured plastic types were weathered under simulated beach conditions for 18 months in freshwater, brackish water, and seawater. Those included polyethylene (PE), polypropylene (PP), polystyrene (PS), polyethylene terephthalate (PET), and polyvinyl chloride (PVC). PP was the first polymer type that fragmented after 9 months of weathering and influenced the pH of the surrounding water. Molecular surface changes were detected for all polymers, just after the first week. Hydroxyl bonds were one of the first groups incorporated into the polymers, weakening 2-3 weeks later. Carbonyl groups were also measured early, but with significantly different developments with time between the polymer types. Differences in degradation rates were proven between the water media, with the fastest degradation in seawater compared to brackish water and freshwater for PE and PP. These results are consistent with previous findings on MPs aged under environmental conditions and provide initial long-term observations of MP degradation pathways under simulated environmental conditions. These findings are valuable for assessing the fate and hazards of MPs in aquatic systems.

First long-term evidence of microplastic pollution in the deep subtropical Northeast Atlantic.

No anthropogenic pollutant is more widespread in the aquatic and terrestrial environment than microplastic; however, there are large knowledge gaps regarding its origin, fate, or temporal variations in the oceans. In this study, we analyzed sediment trap material from the deep subtropical Northeast Atlantic (2000 m) in a long-term record (2003-2015) to assess the role of the deep ocean as a potential sink of microplastics. Microplastic particles were identified in all 110 analyzed samples with flux rates of 1.13-3146.81 items d-1 m-2. Calculated microplastic mass fluxes ranged between 0.10 and 1977.96 µg d-1 m-2, representing up to 8% of the particle flux. Between years, the composition of the different polymers changed significantly, dominated by polyethylene, whose amount was correlated with the lithogenic input. The correlation between polyethylene and the lithogenic fraction was attributed to an air transport pathway from northeast Africa and surrounding regions. The second most abundant polymer detected in our study was polyvinyl chloride, which is not correlated with lithogenic or biogenic particle flux fractions. Instead, we observed seasonality for polyvinyl chloride with recurring high fluxes in winter before the plankton bloom and significantly lower amounts in summer. Other polymers identified were polypropylene, polyethylene terephthalate, and lower numbers of polystyrene and polymethyl methacrylate. The average microplastic particle size for all samples and polymers was 88.44 ± 113.46 µm, with polyethylene and polyvinyl chloride having the highest proportion of small particles (<100 µm). Our findings provide first insights into temporal variations of sinking microplastics, which are crucial for understanding the fate of plastic in the oceans.

Separation of microplastics from mass-limited samples by an effective adsorption technique.

Microplastic in the environment hides visible and invisible dangers for the ecosystems and domiciled organisms. Due to the large quantities of microplastics already distributed worldwide, comparative studies to investigate the associated hazards, distribution patterns, and abundances are becoming increasingly important. Due to varying efforts and budgets, there is still no homogenized detection method for microplastics in the environment, which severely compromises the comparability and reliability of results between previous studies. In this study, we compare the efficacy, degradative effect on microplastics, and microplastic recovery rates of different digestion and separation methods for isolating microplastics from mass-limited environmental samples with high biogenic content. Our results show that the most gentle and effective isolation method is an adsorption-based technique that exploits the lipophilic properties of plastic for separation. This technique achieves an average microplastic recovery rate of 98.0 ± 3.8% and a matrix removal of 96.3 ± 0.3% at low cost and minimum effort. To examine the applicability of this technique to natural environmental samples, eight sediments and two plankton net samples from the South China Sea were selected to determine microplastic abundances. In the analyzed sediment samples, 0-9 microplastic items per 10 g sediment d. w. were found, while 17-25 items per m3 were detected in net samples. Considering the respective mean plastic density, this corresponds to a calculated microplastic mass of 0-39 µg (10 g d.w.)-1 and 3.7-7.1 µg m-3 in sediment and water samples, respectively. This study represents a new way of microplastic extraction from matrix-rich mass-limited samples with high accuracy and easy feasibility at low costs, which would be useful as a worldwide homogenized method in future microplastic research projects and related data comparability.

Abundance and characteristics of microfibers detected in sediment trap material from the deep subtropical North Atlantic Ocean.

Plastics and microplastics increasingly gain importance due to their perils and wide distribution in the marine environment. Microfibers account for the largest percentage of anthropogenic-induced microparticles, which inter alia, consist of plastic, and are found in deep-sea sediments. However, the sinking of fibers from the surface through the water column to the seafloor is still poorly understood. The present study investigates microfibers extracted from sediment trap samples, which were deployed in the North Atlantic Subtropical Gyre (NASG). The average result of eleven analyzed samples showed 913 microfibers per gram of collected particle flux material, with a predominant fiber length shorter than 1 mm (75.6%) and a distribution maximum between 0.2 and 0.4 mm. Further, the average number of microfibers found in this study was used to derive microfiber fluxes for the NASG based on the deployment time of the sediment trap. Extrapolating the computed flux of 94 microfibers m-2 day-1 to the entire NASG area would correspond to a total microfiber mass flux of 9800 t a-1 or 73 × 1013 microfibers a-1 of sinking microfibers through the water column. These findings offer an extended application of sediment traps to monitor microfiber fluxes, which reveals the opportunity to investigate the mechanism driving sinking of microfibers and microplastics into the deep open ocean.