The Ephemare project was supported in the period 2015–2018 by JPI Oceans, as one of 4 sister projects in the joint action on ecological aspects of microplastics. Ephemare investigated several issues concerning the ecotoxicological effects of microplastics (MPs) in marine organisms. Ephemare included 16 European Institutions from 10 Countries and was organized into seven, highly complementary Work Packages (WPs) with the aim to elucidate adsorption and release of chemicals to/from MPs, coupled with MP ingestion rates, translocation in different tissues, trophic transfer and egestion, potential toxicological effects and mechanisms of action, as well as real distributions of MPs in marine organisms from several European areas.

Microplastics are hardly biodegradable and thus accumulate rather than decompose in the environment. Due to sedimentation processes, meiobenthic fauna is exposed to microplastics. Within the meiofauna, nematodes are a very abundant taxon and occupy an important position in benthic food webs by connecting lower and higher trophic levels. However, the key determinants of the uptake of microplastics by freshwater nematodes are still unknown. To investigate the bioaccessibility of microplastics for nematodes, we performed single- and multi-species ingestion experiments in which the ability of seven nematode species (six bacterial and one fungal feeder), diverse in their buccal cavity morphology (1.3–10.5 μm), to ingest fluorescence-labelled polystyrene (PS) beads along with their natural diet was examined. Applied beads sizes (0.5, 1.0, 3.0 and 6.0 μm), exposure time (4, 24 and 72 h) and concentration (3 × 10⁶ PS beads ml⁻¹ and 10⁷ PS beads ml⁻¹) were varied. Ingested beads were localized and quantified via fluorescence microscopy in the nematodes. In contrast to fungal-feeding nematode species with a stylet, bacterial-feeding species ingested 0.5- and 1.0-μm PS beads with up to 249 and 255 beads after 24 h, respectively. Microplastics ≥0.5 μm could only be ingested and transported into the gastrointestinal tract, if the buccal cavities were considerably (>1.3 times) larger than the beads. At concentrations of 10⁷ PS beads ml⁻¹ ingestion rates were influenced by exposure time and PS bead concentration. In case of a known microplastic size distribution in the environment, predictions on the potential ingestion for nematode communities can be made based on the feeding type composition and the size of their buccal cavities.

Microplastics (MPs) are now one of the major environmental problems due to the large amount released in aquatic and terrestrial ecosystems, as well as their diffuse sources and potential impacts on organisms and human health. Still the molecular and cellular targets of microplastics’ toxicity have not yet been identified and their mechanism of actions in aquatic organisms are largely unknown. In order to partially fill this gap, we used a mass spectrometry based functional proteomics to evaluate the modulation of protein profiling in zebra mussel (Dreissena polymorpha), one of the most useful freshwater biological model. Mussels were exposed for 6 days in static conditions to two different microplastic mixtures, composed by two types of virgin polystyrene microbeads (size = 1 and 10 μm) each one. The mixture at the lowest concentration contained 5 × 105 MP/L of 1 μm and 5 × 105 MP/L of 10 μm, while the higher one was arranged with 2 × 106 MP/L of 1 μm and 2 × 106 MP/L of 10 μm.Proteomics’ analyses of gills showed the complete lack of proteins’ modulation after the exposure to the low-concentrated mixture, while even 78 proteins were differentially modulated after the exposure to the high-concentrated one, suggesting the presence of an effect-threshold. The modulated proteins belong to 5 different classes mainly involved in the structure and function of ribosomes, energy metabolism, cellular trafficking, RNA-binding and cytoskeleton, all related to the response against the oxidative stress.

Biodegradable plastics have been introduced and widely used as a promising alternative to traditional nondegradable plastics. However, the differences in sorption behavior of pesticides on nondegradable and biodegradable microplastics has been insufficiently studied. Here, four types of nondegradable [polyethylene (PE), polystyrene (PS), polyvinyl chloride (PVC), polypropylene (PP)] and two types of biodegradable [polylactic acid (PLA), polybutylene succinate (PBS)] microplastics were selected to investigate the sorption mechanism of fipronil based on their sorption kinetics and isotherms. The results indicated that the sorption rates of PLA and PBS were much higher than those of PE, PP, PVC and PS and that the sorption capacities of fipronil on microplastics followed the order of PBS > PLA > PP > PE > PS > PVC. The sorption kinetics followed a pseudo-second-order kinetics model (R² = 0.953–0.998) for all tested microplastics. External mass transport and intraparticle diffusion were the main rate controlling steps of the sorption of fipronil on microplastics. Furthermore, isotherm results indicated that a Langmuir model provided the best fit for fipronil sorption on PE, PS, PVC and PP (R² = 0.997–0.999), while a Freundlich model was the most appropriate model for PLA and PBS (R² = 0.998–0.999). The presence of surface O-containing functional groups and the spatial arrangement of rubbery domains are likely to affect the sorption process. The results from this work suggest that microplastics, especially biodegradable ones, may play an important role in the fate and transport of pesticides, and their effects on soil organisms (e.g., earthworms) require further investigation.

Microplastics (MPs) in the environment have become an issue worldwide. However, data about MPs in freshwater systems are still limited so far. This study investigated sources, fate, and seasonal and spatial distribution of MPs in the main stream Pearl River and its tributaries, as well as in the Pearl River Estuary (PRE), China. MPs were widely detected in the river water, river bed sediment, and estuarine sediment, with abundances of 0.57 ± 0.71 items L⁻¹, 685 ± 342 items kg⁻¹ dry weight (dw), and 258 ± 133 items kg⁻¹ dw, respectively. Sheet, fragmental, and fibrous polyethylene, polypropylene, and ethylene-propylene copolymers were predominant, suggesting that MPs in the Pearl River catchment be mainly derived from fragmentation of discarded plastic wastes. In addition, municipal wastewater was also an important MPs source, especially for polyethylene terephthalate (PET) fibers. Polymers of higher density, such as PET and polyvinyl alcohol were relatively more abundant in the sediment than in the river water, especially in the estuarine sediment. Upward increase of the MP abundance was observed in the sedimentary core, probably indicating increasing release of plastic wastes due to growing production and uses of plastic products. On the other hand, percentage of finer MPs increased with increasing depth. The results revealed persistence and potential downward dispersion of the fine MPs. The MPs abundance was positively related with population density and gross domestic product, demonstrating impacts of human activities and economic development on the MPs contamination. Higher MPs abundance was detected in dry season than in wet season in the river water, suggesting dilution effect of precipitation. It's estimated that 15963 tons of MPs could be released annually into the PRE from the main stream Pearl River and its tributaries.

Microplastic pollution has received considerable attention in marine systems, but recent work shows substantial plastic pollution also occurs in freshwater ecosystems. Most freshwater research has focused on large rivers and lakes, but small streams are the primary interface between land, where plastic is used, and drainage networks. We examined variation in the amount and form of plastic occurring in small streams spanning an urbanisation gradient. All streams contained microplastics with concentrations similar to that found in larger systems (up to 303 particles m−3 in water and 80 particles kg−1 in sediment). The most abundant types were fragments and small particles (63–500 μm). Chemical types of plastic were quite variable and often not predictable based on size, form and colour. Variation in microplastic abundance across streams was high, but only partially explained by catchment scale parameters. There was no relationship between human population density or combined stormwater overflows and microplastic abundance. Residential land cover was related to microplastic abundance, but explanatory power was low. Our results suggest local-scale factors may be more important than catchment-scale processes in determining microplastic pollution in small streams.

Atmospheric transport is an important pathway for the deposition of micro- and nano-plastics in remote areas. However, the sources and fate of atmospheric microplastics remain poorly understood. A study on atmospheric transport and deposition in the Pyrenean Mountains highlights the movement of microplastics away from known sources (cities, agriculture, and industry) into remote areas. Following this first evidence of atmospheric microplastic deposition in a pristine location, it is necessary to reconsider previous studies on atmospheric microplastic deposition and behavior in remote areas.

The accumulation of plastic debris and herbicide residues has become a huge challenge and poses many potential risks to environmental health and soil quality. In the present study, we investigated the transport of glyphosate and its main metabolite, aminomethylphosphonic acid (AMPA) via earthworms in the presence of different concentrations of light density polyethylene microplastics in the litter layer during a 14-day mesocosm experiment. The results showed earthworm gallery weight was negatively affected by the combination of glyphosate and microplastics. Glyphosate and AMPA concentrated in the first centimetre of the top soil layer and the downward transport of glyphosate and AMPA was only detected in the earthworm burrows, ranging from 0.04 to 4.25 μg g−1 for glyphosate and from 0.01 (less than limit of detection) to 0.76 μg g−1 for AMPA. The transport rate of glyphosate (including AMPA) from the litter layer into earthworm burrows ranged from 6.6 ± 4.6% to 18.3 ± 2.4%, depending on synergetic effects of microplastics and glyphosate application. The findings imply that earthworm activities strongly influence pollutant movement into the soil, which potentially affects soil ecosystems. Further studies focused on the fate of pollutants in the microenvironment of earthworm burrows are needed.

Plastic waste is continuously introduced not only into marine, but also freshwater environments, where it fragments into microplastics. Organisms may be affected by the particles themselves due to ingestion and indirectly via incorporated additives such as plasticizers, since these substances have the ability to leach out of the polymer matrix. Although it has been indicated that the likelihood of additives leaching out into the gut lumen of organisms exposed to microplastics is low, studies distinguishing between the effects of the synthetic polymer itself and incorporated additives of the same polymer are scarce. Since this is obligatory for risk assessment, we analyzed the chronic effects of flexible polyvinylchloride (PVC), a widely used polymer, containing the plasticizer diisononylphthalate (DiNP) on morphology and life history of the freshwater crustacean Daphnia magna and compared these effects with the effects of rigid PVC, lacking DiNP, as well as a glass bead control. After up to 31 days of exposure, rigid PVC and glass beads did not affect body length and relative tail spine length of D. magna, whereas flexible PVC led to an increased body length and a reduced number of offspring. None of the treatments increased the mortality significantly. We were able to show that 2.67μg/L DiNP leached out of the flexible PVC into the surrounding medium using GC-MS. Yet, we were not able to measure leachate inside the gut lumen of D. magna. The effects emerged towards the end of the experiment, due to the time dependent process of leaching. Therefore, the results highlight the relevance of long-term chronic exposure experiments, especially as leaching of additives takes time. Further, our study shows the importance to distinguish between microplastics containing leachable additives and the raw polymer in ecotoxicological testing.

The numerical and mass concentrations of microplastics collected at 36 sites on the surfaces of 29 Japanese rivers were mapped and compared with four basin characteristics (basin area, population density, and urban and agricultural ratios) and six water quality parameters (pH, biochemical oxygen demand (BOD), suspended solids (SS), dissolved oxygen (DO), total nitrogen (T-N), and total phosphorus (T-P)) in each river basin. Microplastics were found in 31 of the 36 sites, indicating that some plastics fragment into small pieces before reaching the ocean. The microplastic concentrations are significantly correlated with urbanisation and population density, indicating that the microplastic concentrations in the river depend on human activities in the river basin. Furthermore, we found a significant relationship between the numerical and mass concentrations and BOD, which is an environmental indicator of river pollution. This result demonstrates that microplastic pollution in river environments has progressed more in polluted rivers with poor water quality than in rivers with good water quality, leading to the conclusion that the sources and inflow processes of microplastics in river environments are similar to those of other pollutants. Our findings can help identify potential sources (i.e., point and non-point sources) of fragmented microplastics to improve waste management in Japan and model the transport fluxes of fragmented microplastics in Japanese rivers using water quality parameters and basin characteristics.