Contamination by plastic debris has been documented in most regions of the world, but their occurrence in high mountain areas has not been investigated to date. Here we present the first report of the occurrence and amount of microplastic in any terrestrial glacier environment. In the supraglacial debris of the Forni Glacier (Italian Alps), we observed the occurrence of (mean ± standard error) 74.4 ± 28.3 items kg⁻¹ of sediment (dry weight). This amount is within the range of variability of microplastic contamination observed in marine and coastal sediments in Europe. Most plastic items were made by polyesters, followed by polyamide, polyethylene and polypropylene. We estimated that the whole ablation area of Forni Glacier should host 131–162 million plastic items. Microplastic can be released directly into high elevation areas by human activities in the mountain or be transported by wind to high altitude. The occurrence of microplastic on Forni Glacier may be due to the gathering of debris coming from the large accumulation area into the relatively smaller ablation area of the glacier, as a consequence of its flow and melting.

The Tibet Plateau, the so-called Third Pole of the world, is home to the headstreams of many great rivers. The levels of microplastic pollution in those rivers, however, are unknown. In this study, surface water and sediment samples were collected from six sampling sites along five different rivers. The surface water and sediment samples were collected with a large flow sampler and a stainless steel shovel, respectively. The abundance of microplastics ranged from 483 to 967 items/m3 in the surface water and from 50 to 195 items/kg in the sediment. A large amount of small, fibrous, transparent microplastics were found in this study. Five types of microplastics with different chemical compositions were identified using micro-Raman spectroscopy: polyethylene terephthalate (PET), polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyamide (PA). These results demonstrate that rivers in the Tibet Plateau have been contaminated by microplastics, not only in developed areas with intense human activity but also in remote areas, where microplastic pollution requires further attention.

Microplastic pollution within the marine environment is of pressing concern globally. Accordingly, spatial monitoring of microplastic concentrations, composition and size distribution may help to identify sources and entry pathways, and hence allow initiating focused mitigation. Spatial distribution patterns of microplastics were investigated in two compartments of the southern North Sea by collecting sublittoral sediment and surface water samples from 24 stations. Large microplastics (500−5000 μm) were detected visually and identified using attenuated total reflection (ATR) Fourier transform infrared (FTIR) spectroscopy. The remaining sample was digested enzymatically, concentrated onto filters and analyzed for small microplastics (11−500 μm) using Focal Plane Array (FPA) FTIR imaging. Microplastics were detected in all samples with concentrations ranging between 2.8 and 1188.8 particles kg−1 for sediments and 0.1–245.4 particles m−3 for surface waters. On average 98% of microplastics were <100 μm in sediments and 86% in surface waters. The most prevalent polymer types in both compartments were polypropylene, acrylates/polyurethane/varnish, and polyamide. However, polymer composition differed significantly between sediment and surface water samples as well as between the Frisian Islands and the English Channel sites. These results show that microplastics are not evenly distributed, in neither location nor size, which is illuminating regarding the development of monitoring protocols.

Although evidence suggests the ubiquity of microplastics in the marine environment, our knowledge of its occurrence within remote habitats, such as the deep sea, is scarce. Furthermore, long term investigations of microplastic abundances are even more limited. Here we present a long-term study of the ingestion of microplastics by two deep-sea benthic invertebrates (Ophiomusium lymani and Hymenaster pellucidus) sampled over four decades. Specimens were collected between the years 1976–2015 from a repeat monitoring site >2000 m deep in the Rockall Trough, North East Atlantic. Microplastics were identified at a relatively consistent level throughout and therefore may have been present at this locality prior to 1976. Considering the mass production of plastics began in the 1940s - 50s our data suggest the relatively rapid occurrence of microplastics within the deep sea. Of the individuals examined (n = 153), 45% had ingested microplastics, of which fibres were most prevalent (95%). A total of eight different polymer types were isolated; polyamide and polyester were found in the highest concentrations and in the majority of years, while low-density polystyrene was only identified in 2015. This study provides an assessment of the historic occurrence of microplastics on the deep seafloor and presents a detailed quantification and characterisation of microplastics ingested by benthic species. Furthermore these data advance our knowledge on the long-term fate of microplastic in marine systems.

As a new type of emerging pollutant in the ocean, microplastics have received global attention in recent years. Considering the increasing amount of human activities around the South China Sea, it is important to determine the current status of microplastic pollution in this region. In this study, we analyzed the abundance and distribution of microplastics at Zhubi Reef in the South China Sea. Microplastic abundance ranged from 1,400 to 8,100 items/m3 of surface water, which was much higher than the values reported from other ocean areas. About 80% of the microplastics were smaller than 0.5 mm in size. Fibers and pellets comprised the most common microplastic types. The dominant microplastics were transparent or blue in color. The main polymer types were polypropylene (25%) and polyamide (18%). In general, our results revealed Zhubi Reef was contaminated with microplastics, which were likely derived from the intensive fisheries in the area and emissions from coastal cities. This study also provides baseline data that are useful for additional studies of microplastics in the South China Sea.

Terrestrial environments are subject to extensive pollution by plastics and, based on the slow degradation of plastics, are likely to act as long term sinks for microplastic debris. Currently the hazards of microplastics in soil and the potential impacts on soil organisms is poorly understood. Particularly the role of particle characteristics, such a size or polymer type, in dose-response relationships for microplastics is not known. The aim of this study was to assess the ingestion and toxicity of nylon (polyamide) particles, in three different size ranges, to Enchytraeus crypticus in a soil exposure. Effects were also compared with those of polyvinyl chloride (PVC) particles, in a single size range. Nylon particle ingestion was confirmed using fluorescence microscopy, with greatest ingestion for particles in the smallest size range (13–18 μm). To investigate how particle size affected survival and reproduction, E. crypticus were exposed to nylon particles in two well-defined size ranges (13–18 and 90–150 μm) and concentrations of 20, 50, 90 and 120 g/kg (2–12% w/w). An intermediate nylon size range (63–90 μm) and a larger sized PVC particle (106–150 μm), both at 90 g/kg, were also tested. Survival was not affected by either of the polymer types or sizes. Reproduction was significantly reduced, in a dose-dependent manner, by the nylon particles at high exposure concentrations (>90 g/kg). Smaller size ranges (13–18 μm) had a greater effect compared to larger size ranges (>63 μm), with a calculated EC₅₀ for the 13–18 μm size range of 108 ± 8.5 g/kg. This greater hazard could be qualitatively linked with the ingestion of a greater number of smaller particles. This study highlights the potential for toxic effects of plastics in small size ranges to soil organisms at high exposure concentrations, providing understanding of the hazards microplastics may pose in the terrestrial environment.

Reported here is the first evidence of plastic ingestion by freshwater fishes in the Amazon. Plastic bags, bottles, fishing gear, and other products are entering Amazonian water bodies and degrade into meso- and micro-plastic particles that may be ingested, either directly or indirectly via food chains, by fishes. Examination of stomach contents from 172 specimens of 16 serrasalmid species from lower Xingu River Basin revealed consumption of plastic particles by fishes in each of three trophic guilds (herbivores, omnivores, carnivores). Overall, about one quarter of specimens and 80% of species analyzed had ingested plastic particles ranging from 1 to 15 mm in length. Fourier transform infrared spectroscopy indicated 12 polymer types, including 27% identified as polyethylene, 13% polyvinyl chloride, 13% polyamide, 13% polypropylene, 7% poly(methyl methacrylate), 7% rayon, 7% polyethylene terephtalate, and 13% a blend of polyamide and polyethylene terephtalate. Dimensions of ingested plastic particles varied among trophic guilds, even though the frequency and mass of ingested particles were not significantly different among fishes with different feeding habits.

Microfiber is a subgroup of microplastics and accounts for a large proportion of microplastics in aquatic environment, especially in municipal effluents. The purpose of the present study was to quantify microfiber shedding from three most populate synthetic textile fabrics: polyester, polyamide, and acetate fabrics. The results showed that more microfibers were released after washing with a pulsator laundry machine than a platen laundry machine. The greatest number of microfibers was released from acetate fabric, which was up to 74,816 ± 10,656 microfibers/m2 per wash, although microfibers were shed from all materials. Moreover, an increasing trend was found in the number of microfibers shedding from synthetic fabrics with the washing temperature increasing, and greater microfiber release occurred when washing fabrics with detergent rather than with water alone. The lint filter bag equipped with the pulsator laundry machine retained the longer microfibers (>1000 μm), but not the shorter microfibers (<500 μm) instead of releasing into the drainage system. Our data suggested that microfibers released during washing of synthetic fabrics may be an important source of microfibers in aquatic environment due to the increasing production and use of synthetic fabrics globally. Thus, more efficient filtering bags or other technologies in household washing machines should be developed to prevent and reduce the release of microfibers from domestic washing.

Sinking experiments were conducted using irregularly shaped polyamide (PA), polymethyl methacrylate (PMMA), and polyethylene terephthalate (PET) particles sized 6 to 251 μm. Certified PS spheres were used to validate experiments and showed that the effect of particle size on terminal sinking velocity is well reproduced by the method. As expected sinking velocities of irregularly shaped particles were considerably lower than theoretical values for spheres of the same size range calculated via several approximations available in the literature. Despite the influence of particle shape, the dependence of terminal sinking velocity on particle size can reasonably well be described by a quadratic linear regression, with an average determination of 63%. To generalize results we present a model that predicts terminal sinking velocity as a function of particle size and particle excess density over the fluid. Improving the predictive power of this model requires further experiments with a range of particle characteristics.

Microplastics are becoming a global concern due to their potential to accumulate pollutants in aquatic environments. In this paper, sulfamethazine (SMT) sorption onto six types of microplastics, including polyamide (PA), polyethylene (PE), polyethylene terephthalate (PET), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC) was investigated by experimental and molecular dynamics simulation methods. The experimental results indicated that SMX sorption reached equilibrium within 16 h. The kinetics of SMT sorption by PA, PVC, PE, and PP could be fitted by pseudo first-order model, while SMT sorption by PA and PET could be described by pseudo second-order model. The partition coefficient Kd values were 38.7, 23.5, 21.0, 22.6, 18.6 and 15.1 L·kg⁻¹ for PA, PE, PS, PET, PVC and PP, respectively. SMT sorption onto microplastics decreased when pH and salinity increased. The molecular dynamics simulation results indicated that the main mechanisms involved in sorption are electrostatic and Van der Waals interaction.