Plastic pollution represents the most widespread threaten throughout the world and, amongst aquatic habitats, freshwaters and in particular riparian zones seems to be highly disturbed. Since the plastic storage and accumulation on the riparian vegetation have not yet been deeply investigated, here, we focussed on the riparian zone's function in trapping plastic litter. To do so, we assessed the occurrence and density of plastics in different vegetated (arboreal, shrubby, herbaceous, reed, bush) and unvegetated types in 8 central Italian rivers, running in different land use contexts. Our results showed that plastic pieces, bags, bottles and food containers were the most abundant specific categories on the vegetated types, demonstrating the riparian vegetation role in trapping plastic litter. Specifically, the highest plastic density was found on the shrubby type suggesting that a tree shape retains plastics more easily than all other vegetated and unvegetated types. Shape and size classification of plastics are not significantly different between vegetated and unvegetated types. These findings allow to collect important information on how the riparian vegetation can be exploited in management activities for removing plastic litters from both freshwater and sea, being the former considered the main plastic source for the latter. This study highlights a further ecosystem service as mechanical filter provided by the riparian zone, even if further studies ought to be performed to understand the role of vegetation as plastic trap and the possible detrimental effects of plastics on the plant health status.

Plastic film mulching and use of wastewaters for irrigation have been common agricultural practices for over half a century in Tunisia, especially in arid regions, resulting in the undesired creation of a pathway for microplastics (MPs) to enter farmland soil. In order to assess the extent and characteristics of soil contamination by MPs in the Moknine province, an area of intensive agricultural practices, 16 farmland soil samples were collected and characterized. The total concentration of targeted MPs was 50–880 items/kg; among them, the most common MPs type being polypropylene (PP), mainly occurring as white/transparent fibers with small size (cross section <0.3 mm). SEM images of MPs surfaces revealed multiple features related to environmental exposure and degradation. ATR-FTIR spectroscopy and pyrolysis-GC/MS analyses enabled the accurate identification of MPs separated from the embedding soil micro- and macro-aggregates. Finally, contamination of the polymeric microparticles with a broad range of metals was found by ICP-MS analysis, suggesting that MPs can be vectors for transporting heavy metals in the soil and indicators of soil contamination as a result of mismanagement of industrial wastewaters.

The aim of this study is to assess the occurrence of human litter ingested by arctic foxes (Vulpes lagopus) caught in Svalbard, Norway, in winter when scavenging is at its highest. Twenty arctic fox stomachs and intestines were examined for human litter and plastic using the protocol from the Oslo-Paris Convention (OSPAR) for monitoring plastic ingestion by the northern fulmar (Fulmarus glacialis) (human litter and plastic >1 mm). The arctic foxes had ingested human litter at a low frequency (15%, 3 out of 20 foxes). Despite the low sample size, we do not regard ingestion of human litter as an immediate threat to the arctic fox population in Svalbard.

Polybrominated dibenzo-p-dioxins/furans (PBDD/Fs) and polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) share similar toxicities and thermal origins, e.g., municipal solid waste incinerator (MSWI). Recently, PBDD/Fs from MSWI attracted rising concern because their important precursors, i.e., brominated flame retardants (BFRs), were frequently found in various wastes for landfill or MSWI feedstock. So far, however, little is known about PBDD/Fs and their associated risks in the vicinal environments of MSWI. Here we analyzed PBDD/Fs and PCDD/Fs in 29 soil samples collected around a multiyear large-scale MSWI, and compared their spatial distributions, sources and risks. PBDD/Fs demonstrated comparable concentrations and toxic equivalent quantities (TEQs) to PCDD/Fs in these samples. Spatially, both the concentrations of PBDD/Fs and PCDD/Fs decreased outwards from the MSWI, and exhibited significant linear correlations with the distances from the MSWI in the southeast downwind soil, suggesting the influence of the MSWI on its vicinal soil environment. However, the existence of other dioxin sources concealed its influence beyond 6 km. PBDD/Fs in the soils were characterized by highly-brominated PBDFs, especially Octa-BDF, and their sources were diagnosed as the MSWI and diesel exhaust; PCDD/Fs, however, were dominated by highly-chlorinated PCDDs, particularly Octa-CDD, and were contributed individually or jointly by the MSWI, automobile exhaust and pentachlorophenol (PCP)/Na-PCP. The non-carcinogenic risks of dioxins in all the soil samples were acceptable, but their carcinogenic risks in 17% of the samples were unacceptable. These samples were all located close to the MSWI and highways, therefore, the land use of these two high-risk zones should be cautiously planed.

Intermediate-volatility and semi-volatile organic compounds (I/SVOCs) are key precursors of secondary organic aerosol (SOA). However, the comprehensive characterization of I/SVOCs has long been an analytical challenge. Here, we develop a novel method of speciating and quantifying I/SVOCs using two-dimensional gas chromatography time-of-flight mass spectrometry (GC × GC-ToF-MS) by constructing class-screening programs based on their characteristic fragments and mass spectrum patterns. Using this new approach, we then present a comprehensive analysis of gaseous I/SVOC emissions from heavy-duty diesel vehicles (HDDVs). Over three-thousand compounds are identified and classified into twenty-one categories. The dominant compound groups of I/SVCOs emitted by HDDVs are alkanes (including normal and branched alkanes, 37–66%), benzylic alcohols (7–20%), alkenes (3–11%), cycloalkanes (3–9%), and benzylic ketones (1–4%). Oxygenated I/SVOCs (O–I/SVOCs, e.g., benzylic alcohols and ketones) are first quantified and account for >20% of the total I/SVOC mass. Advanced aftertreatment devices largely reduce the total I/SVOC emissions but increase the proportion of O–I/SVOCs. With the speciation data, we successfully map the I/SVOCs into the two-dimensional volatility basis set space, which facilitates a better estimation of SOA. As aging time goes by, approximate 45% difference between the two scenarios after seven-day aging is observed, which confirms the significant impact of speciated I/SVOC emission data on SOA prediction.

The dispersion of microplastics (MPs) in coastal and marine environments and their potential harmful effects on organisms and ecosystems makes MPs pollution an emerging problem that has gained increasing attention from the scientific community. Despite the recent increase in the number of studies on MPs presence in different marine environments, investigations in Latin America and the Caribbean (LAC) are still relatively limited. This review presents the spatial distribution (where) and the methods applied (how) in assessing MPs contamination on LAC sandy beaches, identifying the challenges to be faced in advancing the understanding of this emerging contaminant. Most of the 39 papers reviewed were published between 2020 and 2021 (51%) and conducted on Brazilian beaches (43%). The LAC investigations apply spot sampling (69%) on shoreline stretches between 10 and 1000 km (59%). These works used inconsistent sampling methods, incomparable techniques for MPs extraction from sediments, and different measurement units to report their data. The MPs presence on LAC beaches is not negligible, as it varies significantly in its distribution and concentration (0–2457 MP/dw kg and 0–5458 MP/m²). Its highest accumulation is on ocean island beaches; however, there are still large stretches of coastline (Cuba, Venezuela, Argentina) with no data on MPs presence and a small number of studies exploring these contaminants' temporal variability. The lack of standardization in the studies’ methodologies, particularly their measurement units, hinders their quantitative comparison and our ability to establish baseline values regarding MPs abundance on LAC beaches. In this sense, future works should direct efforts towards the spatial and temporal expansion of their sampling, as well as protocol standardization to facilitate result comparability on MPs on LAC sandy beaches.

Low-molecular-weight (LMW) phthalate acid esters (PAEs) tend to enter the atmosphere, flying for several kilometers, so it is easy to endanger human health. This work is the first to use quantum chemistry calculations (Gaussian 16 program) and computational toxicology (ECOSAR, TEST, and Toxtree software) to comprehensively study the ozonolysis mechanism of six LMW PAEs (dimethyl phthalate (DMP), diethyl phthalate (DEP), dipropyl phthalate (DPP), diisopropyl phthalate (DIP), dibutyl phthalate (DBP), and diisobutyl phthalate (DIBP)) in the atmosphere and the toxicity of DMP (take DMP as an example) in the conversion process. The results show that the electron-donating effect of the ortho position of the LMW PAEs has the most obvious influence on the ozonolysis. We summarized the ozonation reaction law of LMW PAEs at the optimal reaction site. At 298 K, the law of initial ozonolysis total rate constant of the LMW PAEs is kDIP > kDPP > kDIBP > kDMP > kDEP > kDBP, and the range is 9.56 × 10⁻²⁵ cm³ molecule⁻¹ s⁻¹ — 1.47 × 10⁻²² cm³ molecule⁻¹ s⁻¹. According to the results of toxicity assessment, the toxicity of products is lower than DMP for aquatic organisms after ozonolysis. But those products have mutagenicity, developmental toxicity, non-genotoxicity, carcinogenicity, and corrosiveness to the skin. The proposed ozonolysis mechanism promotes our understanding of the environmental risks of PAEs and provides new ideas for studying the degradation of PAEs in the tropospheric gas phase.

Microplastic pollution is currently one of the most intensely studied ecological issues. Numerous studies have estimated the distribution and concentration of microplastics in various environments and determine how they affect their inhabitants. Much less effort has been place on assessing the possible effects of microplastics on interactions between organisms, including interspecific competition. Our aim was to test the hypothesis that the presence of microplastics affects the proportion of individuals of coexisting species and the elimination rate of the inferior competitor. The hypothesis was tested in competitive experiments done in the absence and presence of spherical non-biodegradable polystyrene and polyethylene and biodegradable polyhydroxybutyrate in environmentally relevant densities. In each of the experiments, we used three different pairs of closely related planktonic species of the genus Daphnia composed of the superior and inferior competitor: D. pulex and D. magna, D. magna and D. galeata, D. pulex and D. galeata. The results support our hypothesis and demonstrate each microplastic type had a different effect on the density of the competing species. The presence of polystyrene and polyethylene lowered the density of the superior competitor in each of the three pairs, at least partially due to a reduction in the number of gravid females, but not their fecundity. The presence of the polyhydroxybutyrate, in turn, increased the population density of D. magna in the variants with each of the two remaining species. Moreover, the presence of microplastics affected the elimination rate of the inferior competitor, i.e. polystyrene expedited the exclusion of D. magna by D. pulex, and polyhydroxybutyrate hampered the exclusion of D. magna by D. pulex. Our results suggest that long-term exposure to environmentally relevant densities of both non-biodegradable and biodegradable microplastics may affect the relative abundance of co-occurring species in zooplankton communities, and thus the functioning of aquatic ecosystems.

In August 2017, after Hurricane Harvey made landfall, almost 52 inches of rain fell during a three-day period along the Gulf Coast Region of Texas, including Harris County, where Houston is located. Harris County was heavily impacted with over 177,000 homes and buildings (approximately 12 percent of all buildings in the county) experiencing flooding. The objective of this study was to measure 13 heavy metals in soil in residential areas and to assess cancer and non-cancer risk for children and adults after floodwaters receded. Between September and November 2017, we collected 174 surface soil samples in 10 communities, which were classified as “High Environmental Impact” or “Low Environmental Impact” communities, based on a composite metric of six environmental parameters. A second campaign was conducted between May 2019 and July 2019 when additional 204 soil samples were collected. Concentrations of metals at both sampling campaigns were higher in High Environmental Impact communities than in Low Environmental Impact communities and there was little change in metal levels between the two sampling periods. The Pollution Indices of lead (Pb), zinc, copper, nickel, and manganese in High Environmental Impact communities were significantly higher than those in Low Environmental Impact communities. Further, cancer risk estimates in three communities for arsenic through soil ingestion were greater than 1 in 1,000,000. Although average soil Pb was lower than the benchmark of the United States Environmental Protection Agency, the hazard indices for non-cancer outcomes in three communities, mostly attributed to Pb, were greater than 1. Health risk estimates for children living in these communities were greater than those for adults.

In the current investigation, we presented the success of the modified hydrothermal method for synthesizing the iron-oxide nanoparticles (Fe₂O₃-NPs) efficiently. These NPs were further characterized by using different techniques such as X-ray diffraction (XRD), scanning electron microscope (SEM) micrographs, energy-dispersive X-ray spectroscopy (EDAX)/Mapping pattern, Raman Spectroscopy Pattern, ultra violet (UV) and Photoluminescence (PL). All these analyses revealed highly pure nature of Fe₂O₃-NPs with no internal defects, and suggested its application for plant growth improvement. Therefore, we further investigated the separate as well as combined effects of the Fe₂O₃-NPs and citric acid (CA) in the alleviation of arsenic (As) toxicity in the soybean (Glycine max L.), by evaluating the different plant growth and metabolic attributes. Results of our study revealed that As-induced growth inhibition, reduction of photosynthesis, water use efficiency (WUE), and reactive oxygen species (ROS) accumulation whereas application of the Fe₂O₃-NPs and CA significantly reversed all these adverse effects in soybean plants. Moreover, the As-stress induced malondialdehyde (MDA) and hydrogen peroxide (H₂O₂) production were partially reversed by the Fe₂O₃-NPs and CA in the As-stressed plants by 16% and 10% (MDA) and 29% and 12% (H₂O₂). This might have resulted due to the Fe₂O₃-NPs and CA induced activities of the antioxidant defense in plants. Overall, the Fe₂O₃-NPs and CA supplementation separately and in combination positively regulated the As tolerance in soybean; however, the effect of the combined application on the As tolerance was more profound relative to the individual application. These results suggested the synergetic effect of the Fe₂O₃-NPs and CA on the As-tolerance in soybean. However, in-depth mechanism underlying the defense crosstalk between the Fe₂O₃-NPs and CA needs to be further explored.