International audience | The role of polyethylene microplastics 4-6 mu m size (MPs) in the toxicity of environmental compounds to fish early life stages (ELS) was investigated. Marine medaka Oryzias melastigma embryos and larvae were exposed to suspended MPs spiked with three model contaminants: benzo(a)pyrene (MP-BaP), perfluorooctanesulfonic acid (MP-PFOS) and benzophenone-3 (MP-BP3) for 12 days. There was no evidence of MPs ingestion but MPs agglomerated on the surface of the chorion. Fish ELS exposed to virgin MPs did not show toxic effects. Exposure to MP-PFOS decreased embryonic survival and prevented hatching. Larvae exposed to MP-BaP or MP-BP3 exhibited reduced growth, increased developmental anomalies and abnormal behavior. Compared to equivalent water-borne concentrations, BaP and PFOS appeared to be more embryotoxic when spiked on MPs than when alone in seawater. These results suggest a relevant pollutant transfer by direct contact of MPs to fish ELS that should be included in the ecotoxicological risk assessment of MPs.

International audience | Due to the dramatic quantity of plastic debris released into our environment, one of the biggest challenges of the next decades is to trace and quantify microplastics (MPs) in our environments, especially to better evaluate their capacity to transport other contaminants such as trace metals. In this study, trace elements (Fe, Cu, Zn, As, Cd, Sn, Sb, Pb, and U) were analyzed in the microplastic subsurface (200 μm) using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Microplastics subjected to the marine environment were collected on beaches (Guadeloupe) exposed to the north Atlantic gyre. We established a strategy to discriminate sorbed contaminants from additives based on the metal concentration profiles in MP subsurface using qualitative and quantitative approaches. A spatiotemporal correlation of the sorption pattern was proposed to compare MPs in terms of relative exposure time and time-weighted average concentrations in the exposure media.

Microplastic debris is ubiquitous and yet sampling, classifying and enumerating this prolific pollutant in marine waters has proven challenging. Typically, waterborne microplastic sampling is undertaken using nets with a 333 μm mesh, which cannot account for smaller debris. In this study, we provide an estimate of the extent to which microplastic concentrations are underestimated with traditional sampling. Our efforts focus on coastal waters, where microplastics are predicted to have the greatest influence on marine life, on both sides of the North Atlantic Ocean. Microplastic debris was collected via surface trawls using 100, 333 and 500 μm nets. Our findings show that sampling using nets with a 100 μm mesh resulted in the collection of 2.5-fold and 10-fold greater microplastic concentrations compared with using 333 and 500 μm meshes respectively (P < 0.01). Based on the relationship between microplastic concentrations identified and extrapolation of our data using a power law, we estimate that microplastic concentrations could exceed 3700 microplastics m⁻³ if a net with a 1 μm mesh size is used. We further identified that use of finer nets resulted in the collection of significantly thinner and shorter microplastic fibres (P < 0.05). These results elucidate that estimates of marine microplastic concentrations could currently be underestimated.

Microplastic pollution in estuarine and coastal environments has recently been characterised in several countries but few researchers have addressed the influence of different forms of coastal zone use on the distribution of microplastic. Here, microplastic particles were sampled in Hangzhou Bay, which is heavily influenced by a range of human activities, and their abundance, size, and polymer type characterised. The abundance of microplastics was 0.14 ± 0.12 items/m³ in water, 84.3 ± 56.6 items/kg dry weight of sediment, and between 0.25 ± 0.14 and 1.4 ± 0.37 items/individual in biota. These results show that Hangzhou Bay has a low level of microplastic contamination compared to other coastal systems in China, although abundance was spatially variable within the bay; relatively higher microplastic abundances were found in the southern area of the bay, which has adjacent industrial and urban land-use zones, while lower abundances were observed in the central and northern bay areas where mariculture, fisheries, and mineral and energy industries are most common. The relatively low microplastic abundance observed in the biota samples is consistent with the generally low values for the seawater and sediment samples. Pellets were the most common of four particle-shape classes (fibres, fragments, films, and pellets) in surface seawater, while fibres were most abundant in sediment and biota. Smaller-sized microplastics (<1.0 mm) were dominant in all samples. Microplastics in the surface seawater were dominated by low-density polypropylene and polyethylene particles, while rayon was dominant in the sediment and biota samples. Our results demonstrate that regional variability in anthropogenic activity and land-use are important controls on the spatial pattern of microplastic pollution in Hangzhou Bay.

Microplastics have attracted much attention in recent years because they are able to interact with other pollutants including pesticides, with implications for the potential risks to biota. However, the sorption behavior of pesticides on microplastics, especially on biodegradable microplastics which are promising alternatives to conventional polymers, has been insufficiently studied. In this study, triadimefon and difenoconazole were selected as model triazole fungicides, and their sorption behavior on a typical biodegradable microplastics (PBS: polybutylene succinate) and two conventional polyethylene (PE) and polyvinyl chloride (PVC) microplastics was investigated with batch experiments in an aqueous solution. PBS presented the highest sorption capacity for triadimefon (104.2 ± 4.8 μg g⁻¹) and difenoconazole (192.8 ± 2.3 μg g⁻¹), which was 1.8- and 1.3-fold that on PE and 4.4- and 7.4-fold that of PVC, respectively. The results of sorption kinetic and isotherm modeling were better fit by a pseudo-second order model and linear model, respectively. More importantly, the effects of environmental factors (pH, salinity and dissolved organic matter) on the sorption behavior were investigated. Fungicide sorption on PBS was generally not affected by salinity, pH or dissolved organic matter. However, in contrast, salinity and dissolved organic matter both significantly decreased sorption on PE and PVC. The results showed that not only the sorption capacities of biodegradable microplastics but also their responses to environmental factors are quite different from those of conventional microplastics. This finding highlights the importance of the role played by biodegradable microplastics in the accumulation and transportation of organic pollutants.

Organic carbon is an essential element for sustainable soil management. While the effects of microplastics on soil physical and biological properties are presenting, it remains unclear whether the organic carbon dynamics of soil are altered by increased microplastic accumulation. The objectives of this study were to evaluate the influences of different polyester microfiber (PMF 0, 0.1% and 0.3% of soil dry weight) and organic material (OM 0, 1%, 2% and 3% of soil dry weight) addition levels on soil organic carbon and to determine the PMF distribution in aggregates from a pot experiment. After 75 days of incubation under 6 wet-dry cycles, the concentrations of soil total organic carbon did not differ significantly between the PMF (9.7 ± 6.6 g kg⁻¹) and control (9.7 ± 6.9 g kg⁻¹) treatments. However, PMF addition significantly reduced the organic carbon concentration in the large (>2 mm) macro-aggregates compared to the control treatment (10.6 ± 4.8 g kg⁻¹ vs. 11.7 ± 4.4 g kg⁻¹), but the results were opposite in the small (2–0.25 mm)macro-aggregates (10.2 ± 4.9 g kg⁻¹ vs. 8.4 ± 3.8 g kg⁻¹). In this study, less than 30% of added PMFs were incorporated into soil aggregates. In addition, the abundance and average length of aggregate-associated PMF in the large (2210 ± 180 particles per g aggregate and 2.08 ± 0.17 mm) and small (1820 ± 150 particles per g aggregate and 1.68 ± 0.11 mm) macro-aggregates were significantly greater than those in the micro-aggregates (1010 ± 70 particles per g aggregate and 0.72 ± 0.05 mm). Our results demonstrate that the distribution of organic carbon in soil macro-aggregates is affected by PMFs addition. Thus, we propose that the behavior of microplastics inside soil aggregates should be further explored to clarify their effects on the physical protection of soil organic carbon.

Despite growing concern about the occurrence of microplastics in aquatic ecosystems there is only rudimentary understanding of the pathways through which any adverse effects might occur. Here, we assess the effects of polystyrene microplastics (PS-MPs; <70 μm) on a common and widespread algal species, Chlorella sorokiniana. We used laboratory exposure to test the hypothesis that the lipids and fatty acids (FAs) are important molecules in the response reactions of algae to this pollutant. Cultivation with PS-MPs systematically reduced the concentration of essential linoleic acid (ALA, C18:3n-3) in C. sorokiniana, concomitantly increasing oleic acid (C18:1n-9). Among the storage triacylglycerols, palmitoleic and oleic acids increased at the expenses of two essential fatty acids, linoleic (LIN, C18:2n-6) and ALA, while PS-MPs had even more pronounced effects on the fatty acid and hydrocarbon composition of waxes and steryl esters. The FA composition of two major chloroplast galactolipids, monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG), were affected implying changes in the conformational structure of photosynthetic complexes in ways that can impair the photosynthesis. These data reveal how exposure to polystyrene microplastics can modify the concentrations of lipid molecules that are important intrinsically in cell membranes, and hence the lipid bilayers that could form an important barrier between algal cellular compartments and plastics in the aquatic environment. Changes in lipid synthesis and fatty acid composition in algae could also have repercussions for food quality, growth and stressor resistance in primary consumers. We advocate further studies of microplastics effects on the lipid composition of primary producers, and of their potential propagation through aquatic food webs.

Microplastics with extremely high abundances are universally detected in marine and terrestrial systems. Microplastic pollution in the aquatic environment, especially in ocean, has become a hot topic and raised global attention. However, microplastics in soils has been largely overlooked. In this paper, the analytical methods, occurrence, transport, and potential ecological risks of microplastics in soil environments have been reviewed. Although several analytical methods have been established, a universal, efficient, faster, and low-cost analytical method is still not available. The absence of a suitable analytical method is one of the biggest obstacles to study microplastics in soils. Current data on abundance and distribution of microplastics in soils are still limited, and results obtained from different studies differ significantly. Once entering into surface soil, microplastics can migrate to deep soil through different processes, e.g. leaching, bioturbation, and farming activities. Presence of microplastics with high abundance in soils can alter fundamental properties of soils. But current conclusions on microplastics on soil organisms are still conflicting. Overall, research on microplastics pollution in soils is still in its infancy and there are gaps in the knowledge of microplastics pollution in soil environments. Many questions such as pollution level, ecological risks, transport behaviors and the control mechanisms are still unclear, which needs further systematical study.

Research on the interaction of microplastics and aquatic organisms has been mainly focused on the evaluation of various impacts on animals while aquatic vascular plants have been so far understudied. In this commentary, we summarized knowledge about interactions of microplastics with aquatic vascular plants and highlighted potential ecological implications. Based on recent research, microplastics have minimal impacts on plants. However, they are strongly attracted to plant tissues, adsorbed, and accumulated by plants. Several mechanisms drive microplastics adsorption and accumulation; the most possibly electrostatic forces, leaf morphology, and presence of periphyton belong among the most important ones. Adsorbed microplastics on plant tissues are easily ingested by herbivores. Plants can thus represent a viable pathway for microplastics to enter aquatic food webs. On the other hand, the strong interactions of microplastics with plants could be used for their phytostabilization and final removal from the environment. Aquatic vascular plants have thus an important role in the behavior and fate of microplastics in aquatic ecosystems, and therefore, they should also be included in the future microplastic research.

Textile microfibers are one of the most important sources within primary microplastics. These have raised environmental concerns since its recent identification as pollutants. However, there are still no accurate models to assess their contribution to the microplastic pollution. Hence, in this study, a method to estimate the mass flow of microfibers detached from household laundry that reaches aquatic environments has been developed. The method considers a set of parameters related to the detachment of microfibers, which are, basically: (1) the detachment rate of microfibers from different textile garments, (2) the volume of laundry effluents, (3) the percentage of municipal water that has been treated, (4) the type of used-water treatment applied, and, (5) the proportion of front- versus top-loading washing machines. In this way, 0.28 million tons of microfibers per year were estimated to reach aquatic environments, which is approximately half than the last published valuation. Finally, hypothetical situations were simulated to evaluate the reduction of microfibers by the modification of some of the parameters at different levels (consumer, government entities, and industry). Thus, depending on the implanted alternatives, microfibers that reach the aquatic environments could be reduced between 30% and 65%.