The seasonal variation and distribution among different matrices of endocrine-disrupting chemicals (EDCs) were investigated in the eutrophic water ecosystem of the Pearl River Delta, Guangdong, China. The chlorophyll a (Chl a) levels were generally higher in summer than in spring; however, the concentrations of 4-tert-octylphenol (OP), 4-nonylphenol (NP), and bisphenol A (BPA) in surface water were generally higher in spring (oligotrophic) than in summer (eutrophic). The levels of EDCs in SPM were lower in spring than in summer, a pattern seen in the seasonal variation of Chl a and particulate organic carbon (POC). The seasonal variations of EDCs in water bodies with different levels of eutrophication were analyzed in several dimensions including sediment, POC, algae and fish bile. The log Kₒc for SPM/water was higher in summer than in spring. The log Kₒc values for NP, OP, and BPA exhibited the following trends between matrices: colloid/water > sediment/water > SPM/water > algae/water, colloid/water > sediment/water > algae/water > SPM/water, and colloid/water > algae/water > sediment/water > SPM/water. The EDCs levels were different in fish tissues with the order bile > liver > muscle, with the concentrations being an order of magnitude higher in bile than in liver and an order of magnitude higher in liver than in muscle. The sequence of the bioconcentration factor (log BCF) for bile/water and liver/water was NP < OP < BPA in eutrophic conditions, but NP > OP > BPA in oligotrophic conditions. The order in eutrophic conditions was the same as the log BCF and log Kₒc for algae/water, indicating that the accumulation of EDCs in water bodies could be affected by algae, which could be one of the reasons of the seasonal variation of EDCs in water.

Particulate matter (PM) emission is one of the leading environmental pollution issues associated with the coal mining industry. Before any control techniques can be employed, however, an accurate prediction of PM concentration is desired. Towards this end, this work aimed to provide an accurate estimation of PM concentration using a hybrid machine-learning technique. The proposed predictive model was based on the hybridazation of random forest (RF) model particle swarm optimization (PSO) for estimating PM concentration. The main objective of hybridazing the PSO was to tune the hyper-parameters of the RF model. The hybrid method was applied to PM data collected from an open-cut coal mine in northern China, the Haerwusu Coal Mine. The inputs selected were wind direction, wind speed, temperature, humidity, noise level and PM concentration at 5 min before. The outputs selected were the current concentration of PM₂.₅ (particles with an aerodynamic diameter smaller than 2.5 μm), PM₁₀ (particles with an aerodynamic diameter smaller than 10 μm) and total suspended particulate (TSP). A detailed procedure for the implementation of the RF_PSO was presented and the predictive performance was analyzed. The results show that the RF_PSO could estimate PM concentration with a high degree of accuracy. The Pearson correlation coefficients among the average estimated and measured PM data were 0.91, 0.84 and 0.86 for the PM₂.₅, PM₁₀ and TSP datasets, respectively. The relative importance analysis shows that the current PM concentration was mainly influenced by PM concentration at 5 min before, followed by humidity > temperature ≈ noise level > wind speed > wind direction. This study presents an efficient and accurate way to estimate PM concentration, which is fundamental to the assessment of the atmospheric quality risks emanating from open-cut mining and the design of dust removal techniques.

Rapid accumulation of aerosol nitrate (NO3−) contributes to haze pollution; however, studies quantifying NO3− formation mechanisms remain scarce. To explore aerosol nitrate formation pathways, total suspended particulate (TSP) samples were collected in Beijing during the spring of 2013, and the concentration of NO3− and δ¹⁸O- NO3− value were analyzed. The NO3− concentrations on polluted days (PD) were higher than those on non-polluted days (NPD). Furthermore, higher δ¹⁸O- NO3− values were observed on PD (86.8 ± 8.1‰) as compared with NPD (73.7 ± 11.0‰) suggest that more nitrate was produced by pathways with relative high δ¹⁸O–HNO₃ values during PD. Based on the calculated δ¹⁸O–HNO₃ values from different formation pathways and the observed δ¹⁸O- NO3− values, the possible fractional contributions of HNO₃ formed via various pathways to TSP NO3− were estimated using the Bayesian isotope mixing model. The δ¹⁸O- NO3− constrained calculations suggest that the pathways of N₂O₅ + H₂O/Cl⁻, NO₃ + VOCs, and ClNO₃ + H₂O possibly contributed 53%–89% to nitrate production during PD. During NPD, the NO₂ + OH pathway produced 37%–69% of the NO3−. Using the δ¹⁸O- NO3− value combined with the isotope mixing model is a promising approach for exploring NO3− formation pathways.

Per- and polyfluoroalkyl substances (PFAS) are widely used in stain-resistant carpets, rugs, and upholstery, as well as in waxes and cleaners, and are potential contaminants in the childcare environment. However, limited knowledge exists on the occurrence of PFAS in indoor environments, apart from residential homes. Here, we determined the occurrence and distribution of 37 neutral and ionic PFAS, including perfluoroalkyl carboxylates (PFCAs) perfluoroalkyl sulfonates (PFSAs), fluorotelomer alcohols (FTOHs), fluorotelomer sulfonates (FTSs), perfluorooctane sulfonamides and perfluorooctane sulfonamidoethanols (FOSAs/FOSEs), and fluorotelomer acrylates and fluorotelomer methacrylates (FTACs/FTMACs) in the childcare environment and estimated children’s exposure through dust ingestion and dermal absorption. We analyzed dust and nap mats, a commonly used item in many childcares, from eight facilities located in the United States. Twenty-eight PFAS were detected in dust with total PFAS concentrations (ΣPFAS) ranging from 8.1 to 3,700 ng/g and were dominated by the two neutral PFAS groups: ΣFTOH (n.d. – 3,100 ng/g) and ΣFOSA/FOSE (n.d. – 380 ng/g). The ionic PFAS were detected at lower concentrations and were dominated by 6:2 FTS and 8:2 FTS (median 12 and 5.8 ng/g, respectively). ΣPFAS concentrations in mats (1.6–600 ng/g) were generally an order of magnitude lower than in dust and were dominated by ΣFOSA/FOSE concentrations (n.d. – 220 ng/g). Daily intake of neutral PFAS in the childcare environment via dust ingestion was estimated at 0.20 ng/kg bw/day and accounted for 75% of the ΣPFAS intake. This higher exposure to neutral PFAS is concerning considering that many neutral PFAS are the precursors of toxic ionic PFAS, such as PFOA.

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.

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.

In this study, the light absorption properties of fine organic aerosols from the burning emissions of four biomass materials were examined using UV-spectrophotometry and Aethalometer-measurements, respectively. For wood chips and palm trees, the burning experiments were carried out with different combustion temperatures (200, 250, and 300 οC) in an adjustable, electrically heated combustor. The light absorptions of water and methanol extracts of aerosols, and smoke particles showed strong spectral dependence on the burning emissions of all biomass materials. However, the burning aerosols of wood chips showed stronger absorption than those of the other biomass burning (BB) emissions. For the burning aerosols of wood chips and palm trees, organic carbon/elemental carbon (OC/EC) decreased as the combustion temperature increased from 200 to 300 °C. Absorption Ångström exponent (AAE) values tended to decrease when combustion temperature increased for smoke aerosols and methanol extracts in smoke samples. The mass absorption efficiency at 365 nm (MAE₃₆₅, m² g⁻¹∙C⁻¹) of water- and methanol-extractable OC fractions was highest in wood chip burning smoke samples. MAE₃₆₅ values of methanol extracts for rice straw, pine needles, wood chips, and palm trees burning emission samples were 1.35, 0.92, 2.36–3.37, and 0.86–1.42, respectively. For wood chip and palm tree burning emissions, AAE₃₂₀–₄₃₀ₙₘ values of methanol extracts were strongly correlated with OC/EC (i.e., combustion temperature) with slopes of 0.11 (p < 0.001) and 0.02 (p < 0.001), and R² values of 0.87 and 0.74, respectively. Moreover, a linear regression between MAE₃₆₅ of methanol extractable OC and OC/EC showed slopes of −0.05 (p < 0.001) and −0.004 (p < 0.001) and R² of 0.72 and 0.74, respectively. The results of this study clearly demonstrate that burning condition and biomass type influence the light absorption properties of organic aerosols from BB emissions.

Abundance, composition, and distribution of macro-litter found on the seafloor of the Strait of Sicily between 10 and 800 m depth has been studied using data collected by bottom trawl surveys MEDITS from 2015 to 2019. Three waste categories based on the items use were considered: single-use, fishing-related and generic-use. Over 600 sampling sites, just 14% of these were litter-free. The five-years average density of seafloor litter was 79.6 items/km² and ranged between 46.8 in 2019 and 118.1 items/km² in 2015. The predominant waste type was plastic (58% of all items). Regardless of material type, single-use items were a dominant (60% of items) and widespread (79% of hauls) fraction of litter with a mean density of 48.4 items/km². Fishing-related items accounted for 12% of total litter items. Percentage of dirty hauls and litter density increased with depth. Analysis of the relation density-depth indicates a progressive increase of litter density beyond depth values situated within the interval 234–477 m depending on the litter category. A significant decrease in litter density by categories was observed over the period. Patterns of spatial distribution at the higher depths (200–80 0m) resulted stable over the years. Density hotspots of fishing-related items were found where the fishing activity that uses fish aggregating devices (FADs) is practised and in the proximity of rocky banks. Single-use and generic-use objects densities were greater on the seafloor along main maritime routes than other areas. Comparisons between the percentage of hauls littered with anthropic waste from the mid-1990s against those in 2018–19 highlighted an increase of about 10.8% and 15.3% for single-use items and fishing-related items respectively, and a decrease of 18.6% for generic-use items. This study provides a snapshot of the current situation of littering in the central Mediterranean Sea and represents a solid baseline against which the effectiveness of current and future mitigation strategies of the litter impact on marine environment can be measured.

This study aims to use ultraviolet (UV) irradiation to decompose polybrominated diphenyl ethers (PBDEs) in the elutes and then reuse the surfactants. The results indicate that UV can remove 2,2′,4,4′-tetrabrominated diphenyl ether (BDE-47) from surfactant eluents and Triton X series surfactants also can remove BDE-47 from the soil. Triton X-100 (TX-100) is the most promising surfactant during the washing and photodegradation processes. Quench experiments suggest that both ¹O₂ and OH• were involved in the TX-100 decomposition but only ¹O₂ is responsible for the degradation of BDE-47. In analysis of the photoproducts of BDE-47 by Gas Chromatography Mass Spectrum (GC-MS) and Liquid Chromatography High Resolution Mass Spectrometry (LC-HRMS), BDE-47 was mainly debrominated to the lower-brominated BDEs and then oxidized to ring-opening products. The little loss of TX-100 can mainly be attributed to the breakage of polyethylene oxide (PEO) chain. Nevertheless, the washing wastes treated by UV light can exhibit higher solubility for BDE-47 than before, indicating they can be reused for BDE-47 removal from soil. The toxicity assessment experiments were performed using Escherichia coli (E.coli) as an indicator. The results indicate that the removal of BDE-47 by UV irradiation can reduce the toxicity of eluent.

The excessive application of manure has caused a high load of phosphorus (P) in the North China Plain. Having an understanding of how manure application affects soil P changes and its transport between different soil layers is crucial to reasonably apply manure P and reduce the associated loss. Based on our 28-year field experiments, the compositions and changes of P species and the risk of P loss under excessive manure treatments were investigated, i.e., no fertilizer (CK), mineral fertilizer NPK (NPK), NPK plus 22.5 t ha⁻¹ yr⁻¹ swine manure (LMNPK), and NPK plus 33.75 t ha⁻¹ yr⁻¹ swine manure (HMNPK). Manure application increased the content of orthophosphate and myo-inositol hexaphosphate (myo-IHP), especially the orthophosphate content exceeded 95%. The amount of orthophosphate in manure and the conversion of organic P to inorganic P in soil were the main reasons for the increased soil orthophosphate. Compared with NPK treatment, soil microbial biomass phosphorus and alkaline phosphatase activity in LMNPK and HMNPK treatments significantly increased. Compared with NPK treatment, a high manure application rate under HMNPK treatment could increase the abundance of organic P-mineralization gene phoD by 60.0% and decrease the abundance of inorganic P-solubilization gene pqqC by 45.9%. Due to the continuous additional manure application, soil P stocks significantly increased under LMNPK and HMNPK treatments. Furthermore, part of the P has been leached to the 60–80 cm soil layer. Segmented regression analysis indicated that CaCl₂–P increased sharply when Olsen-P was higher than 25.1 mg kg⁻¹, however the content of Olsen-P did not exceed this value until 10 years after consecutive excessive manure application. In order to improve soil P availability and decrease the risk of P loss, the manure application rate should vary over time based on soil physicochemical conditions, plants requirements, and P stocks from previous years.