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%.

Plastic, and especially microplastic, contamination of soils has become a novel research field. After the detection of microplastics in soils, spatial distribution and dynamics are still unknown. However, the potential risks associated with plastic particles in soils cannot be sufficiently assessed without knowledge about the spatial distribution of these anthropogenic materials. Based on a spatial research approach, including soil surveys, this study quantified the mesoplastic (MEP, > 5.0 mm) and coarse microplastics (CMP, 2.0–5.0 mm) content of twelve floodplain soils. At four transects in the catchment area of the Lahn river (Germany), soils down to a depth of 2 m were examined for plastic content for the first time. MEP and CMP were detected through visual examination after sample preprocessing and ATR-FTIR analyses. Average MEP and CMP concentrations range between 2.06 kg⁻¹ (±1.55 kg⁻¹) and 1.88 kg⁻¹ (±1.49 kg⁻¹) with maximal values of 5.37 MEP kg⁻¹ to 8.59 CMP kg⁻¹. Plastic particles are heterogeneously distributed in samples. Both plastic size classes occur more frequently in topsoils than in soil layers deeper than 30 cm. The maximal depth of CMP occurrence lies between 75 and 100 cm. Most common CMP polymer type was PE-LD, followed by PP and PA. MEP and CMP particles occur frequently at near channel sides and more often on riparian strips or grassland than on farmland. Vertical distribution of CMP indicates anthropogenic relocation in topsoils and additional deep displacement through natural processes like preferential flow paths or bioturbation. By comparing sedimentation rates of the river with the maximum age of plastic particles, sedimentation as a deposition process of plastic in floodplains becomes probable. From our findings, it can be concluded that an overall widespread but spatial heterogenous contamination occurs in floodplain soils. Additionally, a complex plastic source pattern seems to appear in floodplain areas.

Antimony (Sb) widely occurs in plastics as a pigment and reaction residue and through the use and recycling of electronic material enriched in Sb as a flame retardant synergist. In this study, clean estuarine sediment has been contaminated by different microplastics prepared from pre-characterised samples of different types of plastic (including a rubber) containing a range of Sb concentrations (256–47,600 μg g⁻¹). Sediment-plastic mixtures in a mass ratio of 100:1 were subject to 6-h extractions in seawater and in seawater solutions of a protein (bovine serum albumin; BSA) and a surfactant (taurocholic acid; TA) that mimic the digestive conditions of coastal deposit-feeding invertebrates. Most time-courses for Sb mobilisation could be defined by a second-order diffusion equation, with rate constants ranging from 44.6 to 0.0216 (μg g⁻¹)⁻¹ min⁻¹. Bioaccessibilities, defined as maximum extractable concentrations throughout each time course relative to total Sb content, ranged from <0.01% for a polycarbonate impregnated with Sb as a synergist exposed to all solutions, to >1% for acrylonitrile butadiene styrene containing a Sb-based colour pigment exposed to solutions of BSA and TA and recycled industrial polyethylene exposed to BSA solution. The potential for Sb to bioaccumulate or elicit a toxic effect is unknown but it is predicted that communities of deposit-feeders could mobilise significant quantities of Sb in sediment contaminated by microplastics through bioturbation and digestion.

Pesticides are widely and intensively used in the world for crops protection. High pesticide loadings can potentially pollute the water resource. However, little is known about the usage, environmental emission and fate of pesticides in river basins. Here, we firstly established a pesticide emission estimation method, and investigated the environmental fate of three commonly used pesticides (chlorpyrifos, triazophos, and isoprothiolane) in Dongjiang River basin, southern China using mathematical modelling approach in combination with field monitoring. The distributed hydrological model SWAT (Soil and Water Assessment Tool) was applied to model the emission of the target pesticides from farmland to stream water, and their fate in the basin. A satisfactory model calibration for flow and suspended sediment was obtained based on eight-year observation data of four hydrological monitoring stations in Dongjiang River basin. The differences between the simulation and observation of pesticides were almost within an order of magnitude, including more than 53% differences within 0.5 order of magnitude. In the river basin, 78860 kg of chlorpyrifos, 54990 kg of triazophos and 35320 kg of isoprothiolane were sprayed onto the crops, the estimated annual emissions of the basin come up to 1801 kg, 3779 kg, and 2330 kg under the conditions of rainfall, surface runoff and percolation. After a series of environmental processes including settlement and degradation within the channels, the predicted export masses for chlorpyrifos, triazophos and isoprothiolane were reduced to 266 kg, 1858 kg, 1350 kg, respectively. Successful prediction suggests that the reliable estimation method combing the SWAT modelling can help us understand the source, concentration levels and fate of pesticides in river basin in different scales. Combing the method of emission and fate modelling method we proposed, countries and regions lacking pesticide-application database can facilitate better management of pesticides.

Communities in low-income and middle-income countries (LMIC) are disproportionally affected by industrial pollution compared to more developed nations. This study evaluates the dispersal and associated health risk of contaminant-laden soil and dust at a copper (Cu) smelter in Tsumeb, Namibia. It is Africa’s only smelter capable of treating complex Cu ores that contain high arsenic (As) contents (<1%). The analyses focused on the primary trace elements associated with ore processing at the smelter: As, Cu, and lead (Pb). Portable X-Ray fluorescence spectrometry (pXRF) of trace elements in soils (n = 83) and surface dust wipes (n = 80) showed that elemental contamination was spatially associated with proximity to smelter operations. Soil concentrations were below US EPA soil guidelines. Dust wipe values were elevated relative to sites distal from the facility and similar to those at other international smelter locations (As = 1012 μg/m² (95% CI 687–1337); Cu = 1838 μg/m² (95% CI 1191–2485); Pb = 1624 μg/m² (95% CI 862–2385)). Source apportionment for Pb contamination was assessed using Pb isotopic compositions (PbIC) of dust wipes (n = 22). These data revealed that the PbIC of 73% (n = 16/22) of these wipes corresponded to the PbIC of smelter slag and tailings, indicating contribution from industrial emissions to ongoing exposure risk. Modeling of carcinogenic risk showed that dust ingestion was the most important pathway, followed by inhalation, for both adults and children. Dermal contact to trace elements in dust was also determined to pose a carcinogenic risk for children, but not adults. Consequently, contemporary smelter operations remain an ongoing health risk to the surrounding community, in spite of recent efforts to improve emissions from the operations.

With increasing demand for aquaculture products, water reuse is likely to increase for aquaculture operations around the world. Herein, wastewater stabilization ponds (WSP) represents low cost and sustainable treatment technologies to reduce nutrients and various contaminants of emerging concern from effluent. In the present study, we examined bioaccumulation of selected pharmaceuticals from several therapeutic classes by two important fish species in aquaculture with different feeding preferences (Cyprinus carpio and Sander lucioperca) and their common prey to test whether species specific accumulation occurs. Forty and nineteen from 66 selected pharmaceuticals and their metabolites were positively found in water and sediment samples, respectively from the representative WSP. After a six-month study, which corresponds to aquaculture operations, fourteen pharmaceuticals and their metabolites were detected (at a frequency of higher than 50% of samples) in at least one fish tissue collected from the WSP. We observed striking differences for species and organ specific BAFs among study compounds. Though muscle tissues consistently accumulated lower levels of the target analytes, several substances were elevated in brain, liver and kidney tissues (e.g., sertraline) of both species. Low residual concentrations of these target analytes in aquaculture products (fish fillets) suggest WSPs are promising to support the water-food nexus in aquaculture.

In vitro bioassays have been used as a bioanalytical means of detecting dioxin-like compounds (DLCs) in environmental matrices and have been suggested as a tool for quantifying DLCs in sediments. The present study evaluated the relationship between bioanalytical results from the micro-7-ethoxyresorufin-O-deethylase (EROD) bioassay and chemical analytical results in 25 sediment samples collected from rivers across Germany. Sediments were collected, polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) were extracted from the sediments, biological toxicity equivalent quotients (BEQs) were determined by micro-EROD assay and toxicity equivalent quotients (TEQs) were calculated from chemical analysis. Correlations between BEQs and TEQs were evaluated, and linear regression modeling was performed, excluding 6 samples as validation data, to derive equations for predicting TEQs from BEQs. Validation data was tested to evaluate predictive capabilities of the models. Correlations were observed between BEQ and TEQ for PCDD/Fs (r=0.987), PCBs (r=0.623), measured sum of PCDD/F and PCBs (r = 0.975) and calculated sum of PCDD/F and PCBs (r = 0.971). The modeling equations provided low variances as evaluated by mean absolute error (MAE) (≤10.3 pg/g) and root mean square error (RMSE) (≤15.8 pg/g) indicating that expected TEQs could be reasonably well calculated from BEQs. Predicted TEQs from validation data fell within the 95% probability intervals of the test data and had low variances (MAE≤6.5 pg/g) and (RMSE≤10.7 pg/g). Our results indicate that the micro-EROD bioassay can be used as a screening tool for DLCs in sediment and has the capability to be used as an alternate method to chemical analysis for quantifying dioxin-like potential of sediments.

Ny-Ålesund has been significantly impacted by anthropogenic activities (e.g. coal mining, scientific research, tourist shipping) over the past 100 years. However, the studies of potential toxic elements (PTEs) contamination in Ny-Ålesund currently mainly focus on surface soil or surface fjord sediments, and little is known about the history and status of PTEs contamination over the past 100 years. In this study, we collected a palaeo-notch sediment profile YN, analyzed the contents of six typical PTEs (Cu, Pb, Cd, Hg, As, Se) in the sediments, and assessed the historical pollution status in Ny-Ålesund using the pollution load index, geo-accumulation index and enrichment factor. The results showed that the contents of PTEs over the past 100 years increased rapidly compared with those during the interval of 9400-100 BP. In addition, Pb, Cd and Hg showed a clear signal of enrichment and were the main polluters among the PTEs analyzed. The contamination was likely linked to gas-oil powered generators, coal mining, research station, tourist shipping and long-range transport of pollutants.

The townships of Puchuncaví and Quintero, on the coast of central Chile, have soils contaminated by atmospheric deposition of sulfur dioxide and trace elements from the nearby Ventanas Industrial Complex. The purpose of this study was to evaluate potential human health and ecological risks, by determining the spatial distribution of soil total concentrations arsenic (As), copper (Cu), lead (Pb), and zinc (Zn) in these townships. Total concentrations of these elements were determined in 245 topsoil samples, used to generate continuous distribution maps. The background concentrations of Cu, As, Pb, and Zn in the studied soils were 100, 16, 35, and 122 mg kg⁻¹, respectively. The concentrations of Cu, As, and Pb were positively correlated with each other, suggesting that their source is the Ventanas copper smelter. On the other hand, correlations for Zn were weaker than for other trace elements, suggesting low impact of the Ventanas copper smelter on spatial distribution of Zn. Indeed, only 6% of the study area exhibited Zn concentrations above the background level. In contrast, 77, 32 and 35% of the study area presented Cu, As, and Pb concentrations, respectively, above the background level. The carcinogenic risk due to exposure to As was above the threshold value of 10⁻⁰⁴ in the population of young children (1–5 years old) on 27% of the study area. These risk values are classified as unacceptable, which require specific intervention by the Chilean government. Based on the estimated concentrations of exchangeable Cu, 10, 15, and 75% of the study area exhibited high, medium, and low phytotoxicity risk, respectively.

The aim of the present study was to evaluate the presence of polycyclic aromatic hydrocarbons (PAHs) in oysters (Crassostrea rhizophorae) collected from Todos os Santos Bay (Bahia, Brazil). The total PAH concentration was highest in Madre de Deus (36.3 to 37.8 ng g⁻¹ in dry weight, dw), which is located near a petrochemical complex, oil refinery, and commercial port. In the Paraguaçu river estuary, PAH concentrations varied between 23.2 and 25.7 ng g⁻¹ dw. The lowest concentrations (1.55 ng g⁻¹ dw) were found in the Jaguaribe river estuary, which can be considered a relatively preserved area. The main source of PAHs in the study areas was observed to be pyrogenic. Values of benzo[a]pyrene toxic equivalent ranged from 0.28 to 4.20. The concentrations of PAHs in oysters from the Paraguaçu river estuary and in Madre de Deus indicate the possible lifetime risk of developing cancer in humans who feed on it.