Influence of multiwalled carbon nanotubes with outer diameters > 50 nm (MW) and a surfactant sodium dodecyl benzene sulfonate (SDBS) on bioaccumulation and translocation of pyrene and 1-methylpyrene (1-CH3-pyrene) in maize seedlings in single-(F1) and bi-(F2) compound systems was investigated. Pyrene concentration in shoots was detected in all treatments in F1 and F2, ranging in 10.43–60.28 ng/g and 21.46–40.21 ng/g, respectively, and its translocation factors (TFs) ranged in 0.12–0.19 and 0.07–0.16. However, no 1-CH3-pyrene in shoots was detected from F1 and F2, indicating almost 100% suppression on its translocation from roots to shoots. SDBS at 100 mg/kg significantly enhanced pyrene bioaccumulation in roots and shoots by 43.5% and 77.4% in F1, and 21.7% in roots in F2, while showed insignificant effect on shoot concentration in F2. In contrast, SDBS at 100 mg/kg exerted no significant effect on root 1-CH3-pyrene concentration in F1 and F2. With increasing amendment level of MW from 50 to 3000 mg/kg, both pyrene and 1-CH3-pyrene concentrations in roots and shoots sharply decreased, indicating an increasing suppression on their bioaccumulation and translocation in plant. As for 3000 mg/kg MW + 100 mg/kg SDBS, root concentrations of pyrene and 1-CH3-pyrene in F1 were significantly reduced by 53.4% and 100%, while shoot concentration of pyrene was not affected, generally consistent with the trend of the corresponding bioaccumulation factors (BCFroot) and TFs. As for F2 with the same treatment, root 1-CH3-pyrene concentration declined by 68.6%, whereas pyrene bioaccumulation in roots and shoots was insignificantly affected, which were also in agreement with their BCFroot and TFs. Results of this work highlight the combined impacts of soil amendment with carbon nanotubes and surfactant on bioaccumulation and translocation of pyrene and 1-CH3-pyrene in maize seedlings in multi-pollutant exposure systems, which is important for soil pollution control and food safety assessment.

This work tested a new remediation technology for in-situ degradation of estrogens by delivering a new class of stabilized manganese oxide (MnO2) nanoparticles in contaminated soils. The nanoparticles were prepared using a food-grade carboxymethyl cellulose (CMC) as a stabilizer, which was able to facilitate particle delivery into soil. The effectiveness of the technology was tested using 17β-estradiol (E2) as a model estrogen and three sandy loams (SL1, SL2, and SL3) as model soils. Column transport tests showed that the nanoparticles can be delivered in the three soils, though retention of the nanoparticles varied. The nanoparticle retention is strongly dependent on the injection pore velocity. The treatment effectiveness is highly dependent upon the mass transfer rates of both the nanoparticles and contaminants. When the E2-laden soils were treated with 22–130 pore volumes of a 0.174 g/L MnO(2) nanoparticle suspension, up to 88% of water leachable E2 was degraded. The nanoparticles were more effective for soils that offer moderate desorption rates of E2. Decreasing injection velocity or increasing MnO(2) concentration facilitate E2 degradation. The nanoparticles-based technology appears promising for in-situ oxidation of endocrine disruptors in groundwater.

Experimental work was undertaken to test whether gaseous perfluorooctanoic acid (PFOA) sorbs to glass fibre filters (GFFs) during air sampling, causing an incorrect measure of the gas-particle equilibrium distribution. Furthermore, tests were performed to investigate whether deactivation by siliconisation prevents sorption of gaseous PFOA to filter materials. An apparatus was constructed to closely simulate a high-volume air sampler, although with additional features allowing introduction of gaseous test compounds into an air stream stripped from particles. The set-up enabled investigation of the sorption of gaseous test compounds to filter media, eliminating any contribution from particles. Experiments were performed under ambient outdoor air conditions at environmentally relevant analyte concentrations. The results demonstrate that gaseous PFOA sorbs to GFFs, but that breakthrough of gaseous PFOA on the GFFs occurs at trace-level loadings. This indicates that during high volume air sampling, filters do not quantitatively capture all the PFOA in the sampled air. Experiments with siliconised GFFs showed that this filter pre-treatment reduced the sorption of gaseous PFOA, but that sorption still occurred at environmentally relevant air concentrations. We conclude that deactivation of GFFs does not allow for the separation of gaseous and particle bound perfluorinated carboxylic acids (PFCAs) during active air sampling. Consequently, the well-recognised theory that PFCAs do not prevail as gaseous species in the atmosphere may be based on biased measurements. Caution should be taken to ensure that this artefact will not bias the conclusions of future field studies.

A bioflocculant-producing bacterial strain, designated MSI021, was isolated from the marine sponge Dendrilla nigra and demonstrated 94% flocculation activity in a kaolin clay suspension. MSI021 was identified as Bacillus cereus based on phylogenetic affiliation and biochemical characteristics. The purified extra-cellular bioflocculant was chemically elucidated as a polysaccharide molecule. The polysaccharide bioflocculant was stable under both acidic and alkaline conditions (pH 2.0–10.0) and temperatures up to 100 °C. The purified bioflocculant efficiently nucleated the formation of silver nanoparticles which showed broad spectrum antibacterial activity. The ability of the bioflocculant to remediate heavy metal toxicity was evaluated by measuring the inhibition of bioluminescence expression in Vibrio harveyi. Enrichment of heavy metals such as zinc, mercury and copper at concentrations of 1, 2 and 3 mM in culture media showed significant reduction of bioluminescence in Vibrio, whereas media enriched with heavy metals and bioflocculant showed dose dependent improvement in the expression of bioluminescence. The assay results demonstrated that the polysaccharide bioflocculant effectively mitigates heavy metal toxicity, thereby improving the expression of bioluminescence in Vibrio. This bioluminescence reporter assay can be developed into a high-throughput format to monitor and evaluate of heavy metal toxicity. The findings of this study revealed that a novel polysaccharide bioflocculant produced by a marine B. cereus demonstrated strong flocculating performance and was effective in nucleating the formation antibacterial silver nanoparticles and removing heavy metals. These results suggest that the MSI021 polysaccharide bioflocculant can be used to develop greener waste water treatment systems.

To examine the effects of BaP on tissue apoptosis, laboratory studies were conducted using juvenile Chinese rare minnows (Gobiocypris rarus) exposed to 1, 5, 20, and 80 μg/L of BaP for 28 days. The post-treatment pathological findings in the liver were associated with hepatocyte swelling, karyopyknosis, and karyorrhexis. Moreover, an increase in the goblet cells in the intestine, epithelial hyperplasia of the gills and fusion of gill lamellae were observed. Significant increases in hepatocyte apoptosis using the TUNEL stain were observed in the liver tissue but not in the intestine and gills. In addition, BaP exposure significantly up-regulated the mRNA levels of cyp1a1, p53, bax, bcl-2, and caspase-9 in the liver following the 5, 20, and 80 μg/L treatments, whereas the apaf-1 was significantly down-regulated following all treatments. Moreover, the activities of caspase 3 and caspase 8 were markedly elevated, whereas the protein expression levels of Apaf-1 were down-regulated following the 20 and 80 μg/L treatments. Taken together, our results suggested that BaP strongly induces tissue-specific apoptosis in vivo, leading to significant pathological changes. The responsiveness of apoptotic-related genes demonstrates that BaP induced apoptosis in the liver may be through a mitochondria-independent pathway.

More attention was previously paid to adverse effects of steroids on aquatic organisms and their ecological risks to the aquatic environment. So far, little information has been reported on the bioaccumulative characteristics of different classes of steroids in cultured fish tissues. The present study for the first time provided a comprehensive analysis of the occurrence, bioaccumulation, and global consumers’ health risks via fish consumption of androgens, glucocorticoids and progestanges in typical freshwater cultured farms in South China. The numbers and total concentrations of steroids detected in the tissues of five common species of the cultured fish were in the order of plasma > bile > liver > muscle and plasma > bile, muscle > liver, respectively. The field bioaccumulation factors for the detected synthetic steroids ranged from 450 to 97,000 in bile, 450 to 65,000 in plasma, 2900 to 16,000 in liver, and 42 to 2600 in muscle of fish, respectively. This data suggests that steroids are bioaccumulative in fish tissues. Mostly important, 4-androstene-3,17-dione (AED) and cortisone (CRN) were found to be reliable chemical indicators to predict the levels of steroids in plasma and muscle of the inter-species cultured fish, respectively. Furthermore, the maximum hazard quotients (HQs) of testosterone and progesterone were 5.8 × 10−4 and 9.9 × 10−5, suggesting that human health risks were negligible via ingestion of the steroids-contaminated fish.

Levels of neurotoxic methylmercury (MeHg) in phytoplankton are strongly associated to water MeHg concentrations. Because uptake by phytoplankton is the first and largest step of bioaccumulation in aquatic food webs many studies have investigated factors controlling seasonal changes in water MeHg concentrations. However organic matter (OM), widely accepted as an important driver of MeHg production and uptake by phytoplankton, is known for strong interannual variability in concentrations and composition within systems. In this study, we explore the role of OM on spatial and interannual variability of MeHg in a subarctic coastal sea, the northern Baltic Sea. Using MeHg (2014: 80 ± 25 fM; 2015: <LOD fM; 2016: 21 ± 9 fM) and OM measurements during late summer/early fall, we find that dissolved organic carbon (DOC) and humic matter content explain 60% of MeHg variability. We find that while labile DOC increases MeHg levels in the water, humic content reduces it. We propose that the positive association between MeHg and labile DOC shows that labile DOC is a proxy for OM remineralization rate in nearshore and offshore waters. This is consistent with other studies finding that in situ MeHg production in the water column occurs during OM remineralization. The negative association between water humic content and MeHg concentration is most likely due to humic matter decreasing inorganic mercury (HgII) bioavailability to methylating microbes. With these relationships, we develop a statistical model and use it to calculate MeHg concentrations in late summer nearshore and offshore waters between 2006 and 2016 using measured values for water DOC and humic matter content. We find that MeHg concentrations can vary by up to an order of magnitude between years, highlighting the importance of considering interannual variability in water column MeHg concentrations when interpreting both short and long term MeHg trends in biota.

A quantitative assessment of the vertical profile of traffic pollution, specifically particle number concentration (PNC), in an open space adjacent to a motorway was possible for the first time, to the knowledge of the authors, using an Unmanned Aerial Vehicle (UAV) system. Until now, traffic pollution has only been measured at ground level while the vertical distribution, is limited to studies conducted from buildings or fixed towers and balloons. This new UAV system demonstrated that the PNC sampled during the period form 10 a.m. to 4 p.m., outside the rush hours with a constant traffic flow, increased from a concentration of 2 × 104 p/cm3 near the ground up to 10 m, and then sharply decreased attaining a steady value of 4 × 103 p/cm3 beyond a height of about 40 m. While more comprehensive investigations would be warranted under different conditions, such as topography and vehicle and fuel type, this finding is of great significance, given that it demonstrates the impact of traffic emissions on human exposure, but less so to pollution within the upper part of the boundary layer.

The ubiquitous presence and persistency of microplastics in aquatic environments is of particular concern because these pollutants represent an increasing threat to marine organisms and ecosystems. An identification of the patterns of microplastic distribution will help to understand the scale of their potential effect on the environment and on organisms. In this study, the occurrence and distribution of microplastics in the Bohai Sea are reported for the first time. We sampled floating microplastics at 11 stations in the Bohai Sea using a 330 μm trawling net in August 2016. The abundance, composition, size, shape and color of collected debris samples were analyzed after pretreatment. The average microplastic concentration was 0.33 ± 0.34 particles/m³. Micro-Fourier transform infrared spectroscopy analysis showed that the main types of microplastics were polyethylene, polypropylene, and polystyrene. As the size of the plastics decreased, the percentage of polypropylene increased, whereas the percentages of polyethylene and polystyrene decreased. Plastic fragments, lines, and films accounted for most of the collected samples. Accumulation at some stations could be associated with transport and retention mechanisms that are linked to wind and the dynamics of the rim current, as well as different sources of the plastics.

In this work, a comprehensive characterisation and source apportionment of size-segregated aerosol collected using a multistage cascade impactor was performed. The samples were collected during wintertime in Milan (Italy), which is located in the Po Valley, one of the main pollution hot-spot areas in Europe.For every sampling, size-segregated mass concentration, elemental and ionic composition, and levoglucosan concentration were determined. Size-segregated data were inverted using the program MICRON to identify and quantify modal contributions of all the measured components.The detailed chemical characterisation allowed the application of a three-way (3-D) receptor model (implemented using Multilinear Engine) for size-segregated source apportionment and chemical profiles identification. It is noteworthy that - as far as we know - this is the first time that three-way source apportionment is attempted using data of aerosol collected by traditional cascade impactors. Seven factors were identified: wood burning, industry, resuspended dust, regional aerosol, construction works, traffic 1, and traffic 2. Further insights into size-segregated factor profiles suggested that the traffic 1 factor can be associated to diesel vehicles and traffic 2 to gasoline vehicles. The regional aerosol factor resulted to be the main contributor (nearly 50%) to the droplet mode (accumulation sub-mode with modal diameter in the range 0.5–1 μm), whereas the overall contribution from the two factors related to traffic was the most important one in the other size modes (34–41%).The results showed that applying a 3-D receptor model to size-segregated samples allows identifying factors of local and regional origin while receptor modelling on integrated PM fractions usually singles out factors characterised by primary (e.g. industry, traffic, soil dust) and secondary (e.g. ammonium sulphate and nitrate) origin. Furthermore, the results suggested that the information on size-segregated chemical composition in different size classes was exploited by the model to relate primary emissions to rapidly-formed secondary compounds.