Microcystis aeruginosa (MA) is a primary hazardous cyanobacteria species in aquatic ecosystems that can produce microcystin-LR (MC-LR), which harms aquatic animals. The intestine is an important target tissue for MA and MC-LR. In this study, we investigated the effects of MA and MC-LR exposure on the intestinal microbiota variation and immune responses of Litopenaeus vannamei. Shrimp were experimentally exposed to MA and MC-LR for 72 h. The results showed that both MA and MC-LR exposure caused marked histological variation and apoptosis characteristics and increased oxidative stress in the intestine. Furthermore, the relative expression levels of antimicrobial peptide genes (ALF, Crus, Pen-3) decreased, while those of pro-inflammatory cytokines (MyD88, Rel, TNF-a), a pattern-recognition receptor (TLR4) and a mediator of apoptosis (Casp-3) increased. MA and MC-LR exposure also caused intestinal microbiota variation, including decreasing microbial diversity and disturbing microbial composition. Specifically, the relative abundance of Proteobacteria decreased in the two stress groups; that of Bacteroidetes decreased in the MA group but increased in the MC-LR group, while Tenericutes varied inversely with Bacteroidetes. Our results indicate that MA and MC-LR exposure causes intestinal histopathological and microbiota variations and induces oxidative stress and immune responses in L. vannamei. In conclusion, this study reveals the negative effects of MA and MC-LR on the intestinal health of shrimp, which should be considered in aquaculture.

Airborne particulate matter (PM) contains numerous hazardous polycyclic aromatic hydrocarbons (PAHs) as well as their functionalized congeners. However, the lack of useful methods to identify the sources of PM has hindered the development of researches in atmospheric and public health fields. This report proposes a new method for estimating the source contribution of combustion-derived particulate (Pc) by using 1-nitropyrene (1-NP) and pyrene (Pyr) as markers. This is premised on the fact that the formation of nitrogen oxides in the flame gas and the subsequent nitration of PAHs are functions of combustion temperature and therefore the concentration ratios of NPAHs to PAHs are highly temperature dependent. This method divides combustion sources into two groups - high and low temperatures - which here are respectively represented by automobile engine and coal combustion in urban areas. Formulae are derived for combustion-derived particulate (Pc), whose fraction in the total particulate is y (0 < y < 1), and particulates from combustion sources with high temperatures (Pₕ), whose fraction in Pc is x (0 < x < 1), and low temperatures (Pₗ), whose fraction is (1 －x). When concentrations of 1-NP and Pyr in Pₕ and Pₗ are known, values x and y can be calculated from the formulae by determining atmospheric 1-NP and Pyr concentrations at monitoring sites. Then atmospheric concentrations of Pc, Pₕ and Pₗ can be calculated. The proposed method has been applied for total suspended particulate matter (TSP) samples collected in Kanazawa and Kitakyushu (Japan) and Beijing (China) having different types of atmospheric pollution to clarify the change of contributions of automobiles and coal combustion.

Mono-(2-ethylhexyl) phthalate (MEHP) is the primary monoester transformation product of the commonly used plasticizer, di-2-ethylhexyl phthalate (DEHP), and has been frequently detected in various environmental compartments (e.g., soil, biosolids, plants). Plants growing in contaminated soils can take up MEHP, and consumption of the contaminated plants may result in unintended exposure for humans and other organisms. The metabolism of MEHP in plants is poorly understood, but critical for evaluating the potential human and environmental health risks. The present study represents the first attempt to explore the metabolic fate of MEHP in plants. We used Arabidopsis thaliana cells as a plant model and explored metabolic pathways of MEHP using deuterium stable isotope labelling (SIL) coupled with time-of-flight high resolution mass spectrometer (TOF-HRMS). A. thaliana rapidly took up MEHP from the culture medium and mediated extensive metabolism of MEHP. Combining SIL with TOF-HRMS analysis was proved as a powerful method for identification of unknown MEHP metabolites. Four phase Ⅰ and three phase Ⅱ metabolites were confirmed or tentatively identified. Based on the detected transformation products, hydroxylation, oxidation, and malonylation are proposed as the potential MEHP metabolism pathways. In cells, the maximum fraction of each transformation product accounted for 2.8–56.5% of the total amount of metabolites during the incubation. For individual metabolites, up to 2.9–100% was found in the culture medium, suggesting plant excretion. The results in the cell culture experiments were further confirmed in cabbage and A. thaliana seedlings. The findings suggest active metabolism of MEHP in plants and highlight the need to include metabolites in refining environmental risk assessment of plasticizers in the agro-food systems.

Clonal plants can share information and resources among connected ramets (asexual individuals). Such clonal integration can promote ramet growth, which may further influence soil microbial communities in the rooting zone. Crude oil contamination can negatively affect plant growth and alter soil microbial community composition. However, we still know little about how clonal integration affects soil microbial communities, especially under crude oil contamination. In a coastal wetland, ramets of the rhizomatous plant Phragmites australis in circular plots (60 cm in diameter) were subjected to 0, 5 and 10 mm depth of crude oil, and the rhizomes at the edge of the plots were either severed (preventing clonal integration) or left intact (allowing clonal integration). After three years of treatment, we analysed in each plot soil physiochemical properties and soil microbial community composition. The alpha-diversity of the soil microbial communities did not differ between intact and severed plots, but was overall lower in 10-mm than in 0-mm and 5-mm oil plots. Considering all three oil treatments together, soil microbial community dissimilarity (beta-diversity) was positively correlated with soil property distance in both severed and intact plots. Considering the three oil treatments separately, this pattern was also observed in 10-mm oil plots, but not in 0-mm or 5-mm oil plots. The soil microbial community composition was more sensitive to the oil addition than to the clonal integration. Moreover, the relative abundance of the nitrogen-cycling bacterial taxa was lower in intact than in severed plots, and that of the oil-degrading bacterial taxa increased with increasing oil-addition levels. Our results indicate that clonal integration and oil contamination can influence soil microbial communities independently through changing the relative abundance of the component bacteria taxa, which has important implications for ecosystem functions of the soil food web mediated by clonal plants.

Breaking of biochar during compaction of amended soil in roadside biofilters or landfill cover can affect infiltration and pollutant removal capacity. It is unknown how the initial biochar size affects the biochar breaking, clogging potential, and contaminant removal capacity of the biochar-amended soil. We compacted a mixture of coarse sand and biochar with sizes smaller than, similar to, or larger than the sand in columns and applied stormwater contaminated with E. coli. Packing columns with biochar pre-coated with a dye and analyzing the dye concentration in the broken biochar particles eluted from the columns, we proved that biochar predominantly breaks under compaction by disintegration or splitting, not by abrasion. Increases in biochar size decrease the likelihood of biochar breaking. We attribute this result to the effective dissipation of compaction energy through a greater number of contact points between a large biochar particle and the adjacent particles. Most of the broken biochar particles are deposited in the pore spaces of the background geomedia, resulting in an exponential decrease in hydraulic conductivity of amended sand with an increase in suspended sediment loading. The clogging rate was higher in the columns with small biochar. The columns with small biochar also exhibited high E. coli removal capacity, partly because of an increase in bacterial straining at reduced pore size after compaction. These results are useful in selecting appropriate biochar size for its application in soils and roadside biofilters for stormwater treatment.

The biofiltration capacity of bivalve populations is known to alleviate the effects of coastal eutrophication. However, this important ecosystem service could potentially be impaired by the increasing microplastic abundance in near shore environments. It is known that relatively large microplastics (∼500 μm) impair the filtration capacity of bivalves. However, the effect of smaller microplastics, and specifically microfibers, is not known even though they are more common in many natural systems and similar in size to phytoplankton, the main food source of mussels. Here, we investigated the effects of long-term exposure to microfibers (MFs), which are smaller than 100 μm, on the biofiltration capacity of the blue mussel, Mytilus edulis. Our findings show that long-term exposure (here 39 days) to microfibers significantly reduced (21%) the clearance of phytoplankton (Tetraselmis sp). While previous studies have shown that larger microplastics can decrease the filtration capacity of mussels after short-term exposure, our findings suggest that, for smaller MFs, mussel’s clearance capacity is significantly affected after long-term exposure (39 days in this study). This may be due to the accumulation of MFs in the digestive system. In addition, the most efficient phytoplankton consumers were more susceptible to MF accumulation in the digestive system. This suggests that prolonged exposure to MF of coastal mussels could negatively impact the biofiltration of more potent individuals, thus decreasing the ecosystem service potential of the population as a whole.

Silver nanoparticles (AgNPs) are expected to enter aquatic systems, but there are limited data on how they might affect microbial communities in pathogen impaired streams. We examined microbial community responses to citrate-AgNP (10.9 ± 0.7 nm) and polyvinylpyrrolidone (PVP)–AgNP (11.0 ± 0.7 nm) based on microbial concentration and enzyme activity in sediment from a pathogen impaired stream. Addition of each nanoparticle to sediment caused at least a 69% decrease in microbial concentration (1,264 ± 93.6 to 127 ± 29.5 CFU/g) and a 62% decrease in β-glucosidase activity (11.7 ± 2.1 to 1.3 ± 0.3 μg/g/h). Each AgNP reduced alkaline phosphatase activity but their effects were not statistically significant. Sediment exposed to 0.108 mg Ag/kg of AgNO₃ resulted in a 92% decrease in microbial concentration and a reduced enzyme activity which was not statistically significant. Measured total silver in sediments treated with AgNPs which exhibited significant inhibition effects on the microbial community ranged from 0.19 ± 0.02 to 0.39 ± 0.13 mg Ag/kg. These concentrations tested in this study are much lower than the expected concentrations (2–14 mg Ag/kg) in freshwater sediments. The results of this study demonstrate that AgNPs can alter microbial community activity and population size, which may lead to false negative fecal indicator bacteria detection and enumeration using methods that rely on β-glucosidase activity. We conclude that the presence of AgNPs in impaired streams and recreational waters can influence pathogen detection methods, potentially affecting public health risk estimates.

The objective of the present study was to investigate recent concentrations of perfluoroalkyl substances (PFASs) in white whales (Delphinapterus leucas) from Svalbard and compare them to concentrations found in white whales sampled from that same area 15 years ago. Plasma collected from live-captured white whales from two time periods (2013–2014, n = 9, and 1996–2001, n = 11) were analysed for 19 different PFASs. The 11 PFASs detected included seven C₈–C₁₄ perfluoroalkyl carboxylates (PFCAs) and three C₆–C₈ perfluoroalkyl sulfonates (PFSAs) as well as perfluorooctane sulfonamide (FOSA). Recent plasma concentrations (2013–2014) of the dominant PFAS in white whales, perfluorooctane sulfonate (PFOS; geometric mean = 22.8 ng/mL), was close to an order of magnitude lower than reported in polar bears (Ursus maritimus) from Svalbard. PFOS concentrations in white whales were about half the concentrations in harbour (Phoca vitulina) and ringed (Pusa hispida) seals, similar to hooded seals (Cystophora cristata) and higher than in walruses (Odobenus rosmarus) from that same area. From 1996 to 2001 to 2013–2014, plasma concentrations of PFOS decreased by 44%, whereas four C₉₋₁₂ PFCAs and total PFCAs increased by 35–141%. These results follow a similar trend to what has been reported in other studies of Arctic marine mammals from Svalbard. The most dramatic change has been the decline of PFOS concentrations since 2000, corresponding to the production phase-out of PFOS and related compounds in many countries around the year 2000 and a global restriction on these substances in 2009. Still, the continued dominance of PFOS in white whales, and increasing concentration trends for several PFCAs, even though exposure is relatively low, calls for continued monitoring of concentrations of both PFCAs and PFSAs and investigation of biological effects.

China has been in the implementation phase of Domestic Ship Emission Control Areas (DECAs) regulation to reduce emissions of air pollutants from ships near populated areas since 2016. The Yangtze River Delta (YRD) is one of the busiest port clusters in the world, accounting for 11% of global seaborne cargo throughput, so future improvements in shipping emission controls may still be important in this region. To assess the impact of future ship emissions on air quality of coastal areas, this study evaluates emissions reductions and air quality in 2030 for three scenarios (business as usual, stricter regulations, and aspirational policies) representing increasing levels of control compared with a base year of 2015. We projected ship emissions in the region using a bottom-up approach developed in this study and based on the historical ship automatic identification system (AIS) activity data. We then predicted air quality across the YRD region in 2030 using the Community Multiscale Air Quality (CMAQ) model. The annual average contributions of ship emissions to ambient PM₂.₅ would decrease by 70.9%, 80.4%, and 86.2% relative to 2015 under the three scenarios, with the largest reductions of more than 4.1 μg/m³ near Shanghai Port under the aspirational scenario. Reductions in ship emissions generally led to lower levels of PM₂.₅, particularly in most of the coastal cities in the YRD. Compared with a business-as-usual approach the aspirational scenario reduced SO₂, NOₓ and PM₂.₅ concentrations from shipping by 71.8%, 61.1% and 52.5%, respectively. It was also more effective than the stricter regulation scenario, suggesting that the requirement to use 0.1% sulfur fuel within a 100Nm DECA would have additional benefits to ambient PM₂.₅ concentrations beyond 12Nm DECA area. This study provides evidence to inform deliberations on the potential air quality benefits of future control policies for ship emissions in China.

Bisphenol A (BPA) is a widely produced chemical that is mainly used as raw material for manufacturing plastic products. It is an endocrine disruptor and causes irreversible damage to the human body. Bisphenol S (BPS), an alternative to BPA, has low dose effects on toxicology and genotoxicity. Herein, we constructed a highly porous crystalline covalent organic framework (COF, CTpPa-2)-modified glassy carbon electrode (GCE) for the electrochemical sensing of BPA and BPS. The electrochemical properties of the CTpPa-2/GCE were characterized using galvanostatic charge-discharge, cyclic voltammetry and differential pulse voltammetry. The CTpPa-2/GCE exhibited remarkable electrocatalytic activity, and the electrochemical responses for BPA and BPS were found to be linear in the concentration ranges of 0.1–50 μM and 0.5–50 μM with detection limits of 0.02 μM and 0.09 μM (S/N = 3), respectively. Moreover, the fabricated sensor was utilized to determine BPA and BPS in bottle samples with recoveries of 87.0%–92.2% and migration rates of 13.2%–28.0%.