Volatile organic compounds (VOCs) has consistently been linked to ozone (O₃) and secondary organic aerosol (SOA) formation, and ongoing emission policies are primarily focusing on total VOCs without addressing the association between regulation measures and secondary pollution characteristic. For enhancing VOCs emission policy, we investigated potential formation of O₃ and SOA based on analyses of node-specific VOCs concentration and species distribution in solvent-consuming industry. Although aromatics were found to contribute most to O₃ and SOA formation averagely (2.57 ± 2.14 g O₃/g VOCs, 1.91 ± 1.67 g SOA/g VOCs), however, large disparity concerning emission and secondary pollution profile were identified among different emission nodes which demonstrated that regulation policy should be formulated based on comprehensive pollution characteristic. Therefore, emission nodes were classified into four clusters through data normalization, formatting and classification process, including aromatics dominated (7 emission nodes), aromatics-alkene dominated (4 emission nodes), aromatics-alcohols dominated (4 emission nodes) and alcohols dominated (4 emission nodes). And different dominating VOCs species were further obtained in each cluster. Subsequently, focusing regulation measures of reducing O₃ and SOA for different emission source clusters were proposed to guide pollution prevention and enhance future VOCs emission policies.

Exposure to environmental endocrine disrupting chemicals (EDCs) is highly suspected in prostate carcinogenesis. Though, estrogenicity is the most studied behavior of EDCs, the androgenic potential of most of the EDCs remains elusive. This study investigates the androgen mimicking potential of some common EDCs and their effect in androgen-dependent prostate cancer (LNCaP) cells. Based on the In silico interaction study, all the 8 EDCs tested were found to interact with androgen receptor with different binding energies. Further, the luciferase reporter activity confirmed the androgen mimicking potential of 4 EDCs namely benzo[a]pyrene, dichlorvos, genistein and β-endosulfan. Whereas, aldrin, malathion, tebuconazole and DDT were reported as antiandrogenic in luciferase reporter activity assay. Next, the nanomolar concentration of androgen mimicking EDCs (benzo[a]pyrene, dichlorvos, genistein and β-endosulfan) significantly enhanced the expression of AR protein and subsequent nuclear translocation in LNCaP cells. Our In silico studies further demonstrated that androgenic EDCs also bind with epigenetic regulatory enzymes namely DNMT1 and HDAC1. Moreover, exposure to these EDCs enhanced the protein expression of DNMT1 and HDAC1 in LNCaP cells. These observations suggest that EDCs may regulate proliferation in androgen sensitive LNCaP cells by acting as androgen mimicking ligands for AR signaling as well as by regulating epigenetic machinery. Both androgenic potential and epigenetic modulatory effects of EDCs may underlie the development and growth of prostate cancer.

As an emerging brominated flame retardant (BFR), tetrabromobisphenol S (TBBPS) has been frequently detected in the environmental media and organisms. Knowledges on the transformation and fate of TBBPS in both environment and engineering systems are essential to its ecological risk assessment. Herein, we reported the photochemical decomposition of TBBPS in aqueous solution upon 254 nm ultraviolet irradiation (UV₂₅₄). Results show that TBBPS was highly photoreactive, most likely due to the presence of four ortho-bromine substituents. The molar absorption coefficient and quantum yield of TBBPS were found to be pH-dependent, with the monoanionic form being most photoreactive. A series of photoproducts were identified by solid phase extraction (SPE) combined with liquid chromatography-electrospray ionization-triple quadrupole mass spectrometry (LC-ESI(+)-MS/MS. The photolysis of TBBPS likely proceeded through photonucleophilic substitution, photoreductive debromination, and β-scission reactions. A ketocarbene, possibly derived from the lower lying excited triplet state, was proposed to be involved in the photolysis of TBBPS. Ion chromatography analysis revealed that debromination occurred quickly, and the yield of bromide (Br⁻) approached 100% after 90 min irradiation. The presence of SRNOM and MRNOM inhibited the photodegradation rate of TBBPS, which is likely due to the light-screening and physical quenching effects of natural organic matter (NOM). Our results reveal that photolysis is an important process for the attenuation of TBBPS in aquatic system; however, naturally occurring species such as NOM can appreciably retard the decay of TBBPS.

Multidisciplinary approaches are essential to diligently assess environmental health status of ecosystems. In this study, year-round chemical elements' exposure and impacts were assessed on the wide-ranging Cory's shearwater Calonectris borealis breeding in Berlenga Island, offshore Portugal, North Atlantic Ocean. The aim was to identify potential contamination and oxidative stress sources associated with trophic ecology, habitat and spatial use, and foraging patterns. A set of 20 chemical elements were quantified, along with oxidative stress biomarkers, stable isotope analyses, and GPS tracking data. Birds presented higher accumulation to some non-essential elements along the year (i.e. arsenic, As; cadmium, Cd; mercury, Hg; lead, Pb; and strontium, Sr), in which concentrations were similar or surpassed other procellariform seabird populations all over the world. No significant differences were found for any of the elements between different periods within the breeding season, with exception of Hg. However, a Principal Component Analysis taking into consideration a group of elements showed differences between pre-laying and chick-rearing periods, with overall higher concentrations in the former. Individuals spending more time engaging in an intensive search for food, and in more coastal environments, presented overall higher element concentrations, and particularly Hg. Contrary to expectations, no relationships were found between chemical elements and oxidative stress. On the other hand, spatial use and foraging patterns of Cory's shearwaters influenced their oxidative stress responses. Our results highlight the need for multidisciplinary approaches to deepen understanding of the large-scale vulnerability of bioindicators such as seabirds and, by extension, the overall environmental health of ecosystems in which they rely.

Due to a close contact with water column, submerged macrophytes are easily disturbed by environment change in freshwater ecosystems, especially at the seedling stage. In recent decades, freshwater ecosystems have been subject to severe cadmium (Cd) pollution, which can cause toxic effects on the growth of submerged macrophytes. Moreover, the temperature rise resulting from climate warming and water level decline may further aggravate such effect, especially in shallow lakes. Here, we investigated the independent and interaction effects of Cd exposure levels (0, 0.5, 1, and 2.5 mg L⁻¹) and temperature (15, 25, and 30 °C) on morphological and physiological traits of Myriophyllum aquaticum (Vell.) Verd. Seedlings generated from propagules and seeds. The temperature rise and Cd exposure generally resulted in a significant increase of Cd concentrations and antioxidant enzyme activities in leaves, as well as a decrease of chlorophyll a and b concentrations. The number and length of leaves generated from propagules always show a downward trend with the increase of Cd exposure, regardless of the temperature. Moreover, the lowest leaf number and length always occurred at high temperature (i.e. 30 °C) when the Cd exposure level increased to 1 and 2.5 mg L⁻¹. For the seedlings generated from seeds, the temperature rise caused an increase of leaf emergence rate under low Cd exposure levels, but resulted in a significant decrease with the Cd exposure level. This study indicates the negative effects of Cd exposure and temperature rise on submerged macrophytes at the seedling stage, and highlights that temperature rise would enhance Cd toxicity.

Nitrogen (N) runoff loss from croplands due to excessive anthropogenic N additions is a principal cause of non-point source water pollution worldwide. Quantitative knowledge of regional-scale N runoff loss from croplands is essential for developing sustainable agricultural N management and efficient water N pollution control strategies. This meta-analysis quantifies N runoff loss rates and identifies the primary factors regulating N runoff loss from uplands (n = 570) and paddy (n = 434) fields in the Yangtze River Basin (YRB). Results indicated that total N (TN) runoff loss rates from uplands and paddy fields consistently increased from upstream to downstream regions. Runoff depth, soil N content and fertilizer addition rate (chemical fertilizer + manure) were the major factors regulating variability of TN runoff loss from uplands, while runoff depth and fertilizer addition rate were the main controls for paddy fields. Multiple regression models incorporating these influencing factors effectively predicted TN runoff loss rates from uplands (calibration: R² = 0.60, n = 242; validation: R² = 0.55, n = 104) and paddy fields (calibration: R² = 0.70, n = 189; validation: R² = 0.85, n = 82). Models estimated total cropland TN runoff loss load in YRB of 0.54 (95% Cl: 0.23–1.33) Tg, with 0.30 (95% Cl: 0.15–0.56) Tg from uplands and 0.24 (95% Cl: 0.08–0.77) Tg from paddy fields in 2017. Guangxi, Jiangxi, Fujian, Hunan and Henan provinces within the YRB were identified as cropland TN runoff loss hotspots. Models predicted that TN runoff loss loads from croplands in YRB would decrease by 0.8–13.7% for five scenarios, with higher TN load reductions occurring from scenarios with decreased runoff amounts. Reducing upland TN runoff loss should focus primarily on soil N utilization and runoff management, while reducing N fertilizer addition and runoff provided the most sensitive strategies for paddy fields. Integrated management of water, soil and fertilizer is required to effectively reduce cropland N runoff loss.

One of the worst socio-environmental disasters to mark the history of Brazil and the world occurred in November 2015 and involved the mining sector. The collapse of the Fundao dam released approximately 43 million m³ of iron ore tailings, which moved downstream to reach the Doce River. This resulted in the contamination of water, soil, and sediments along the entire course of the river, which also affected its mouth in the Atlantic Ocean. Four years after the disaster, several socio-environmental problems continue to persist in the affected areas. In this context, the reservoirs built along the Doce River deserve special attention as they are artificial environments that are highly vulnerable to changes in water parameters. This study aims to determine water quality indicators of these reservoirs using remote sensing data and image processing methods, including semi-analytical algorithms, to comprehend the progress of eutrophication processes. Operational land imager/Landsat-8 data (from 2013 to 2019) were used to map the suspended particulate matter (SPM), euphotic zone (Zₑᵤ) and chlorophyll-a (Chl-a) before and after the collapse. The results showed significant changes in SPM and Zₑᵤ in the reservoirs after the collapse. Non-conformity of these parameters is observed even now, and they tend to intensify during rainy periods when resuspension processes of sediments occur. Moreover, there has been an increase in the eutrophication of reservoirs as noticed by the significant increase in Chl-a after the disaster, especially in January, July, and August.

It is highly likely that the toxicity of water accommodated fractions (WAF) will influence marine microalgae, and consequently lead to potential risk for the marine ecological environment. However, it was often neglected whether WAF can influence the transformation of relative compounds in organisms. The metabolism of amino acids (AAs) can be used to track physiological changes in microalgae because amino acids are the basis of proteins and enzymes. In this study, using marine Chlorophyta Platymonas helgolandica as the test organism, the effects of different concentrations of WAF on AA compositions and stable carbon isotope ratios (δ¹³C) of individual AAs of Platymonas helgolandica were investigated. The results showed that the WAF of #180 fuel oil had an obvious suppressing effect on the growth and chlorophyll a content of microalgae. The growth inhibitory rate at 96 h was 80.66% at a WAF concentration of 0.50 mg L⁻¹ compared with the control. Furthermore, seven among the 16 AAs, including alanine, cysteine, proline, aspartic acid, lysine, histidine and tyrosine, had relatively high abundance. Under the glycolysis pathway, the cysteine abundance was higher than control, meaning that the biosynthesized pathway of alanine through cysteine as a precursor could be damaged. Phosphoenolpyruvate (PEP) was an important synthesis precursor of alanine (leucine) and aromatic AA family (Phenylalanine and tyrosine), and played an important role in δ¹³CAAₛ fractionation under the WAF stress. Under the TCA pathway, to protect cell metabolism activities under WAF stress, the δ¹³C value of threonine and proline abundance in microalgae with the increase in WAF stress. Therefore, δ¹³CAAₛ fractionation can be used as a novel method for toxicity evaluation of WAF on future.

Polycyclic aromatic compounds (PACs) in Canadian air and deposition were examined at the national scale for the first time in over twenty-five years. Air concentrations spanned four orders of magnitude, and were highest near industrial emitters and lowest in the Arctic. Declines in unsubstituted PAHs were observed at locations close to industrial facilities that had reduced emissions, but trends elsewhere were modest or negligible. Retene concentrations are increasing at several locations. Ambient concentrations of benzo[a]pyrene exceeded Ontario’s health-based guideline in many urban/industrial areas. The estimated toxicity of the ambient PAC mixture increased by up to a factor of six when including compounds beyond the US EPA PAHs. Knowledge of PAC deposition is limited to the Laurentian Great Lakes and Athabasca Oil Sands regions. The atmosphere remained a net source of PAHs to the Great Lakes, though atmospheric inputs were decreasing with halving times of 26–30 years. Chemical transport modelling substantially overestimated wet deposition, but model performance is unknown for dry deposition. Sources from Asia, Europe and North America contributed to Arctic and Sub-Arctic concentrations, whereas transboundary or long-range transport have not been assessed outside Canada’s north. Climate-related impacts from re-emission and forest fires were implicated in maintaining air concentrations in the high Arctic that were not consistent with global emissions reductions. Industrial emission decreases were substantial at the national scale, but their influence on the environment was limited to areas near relevant facilities. When examined through the lens of ambient levels at the local scale, evidence suggested that contributions from residential wood combustion and motor vehicles were smaller and larger, respectively, than those reported in national inventories. Future work aimed at characterizing PACs beyond the EPA PAHs, improving measurement coverage, elucidating deposition phenomena, and refining estimates of source contributions would assist in reducing remaining knowledge gaps about PACs in Canada.

Water pollution by microplastics (MPs) is a contemporary issue which has recently gained lots of attentions. Despite this, very limited studies were conducted on the degradation of MPs. In this paper, we reported the treatment of synthetic mono-dispersed suspension of MPs by using electrooxidation (EO) process. MPs synthetic solution was prepared with distilled water and a commercial polystyrene solution containing a surfactant. In addition to anode material, different operating parameters were investigated such as current intensity, anode surface, electrolyte type, electrolyte concentration, and reaction time. The obtained results revealed that the EO process can degrade 58 ± 21% of MPs in 1 h. Analysis of the operating parameters showed that the current intensity, anode material, electrolyte type, and electrolyte concentration substantially affected the MPs removal efficiency, whereas anode surface area had a negligible effect. In addition, dynamic light scattering analysis was performed to evaluate the size distribution of MPs during the degradation. The combination of dynamic light scattering, scanning electron microscopy, total organic carbon, and Fourier-transform infrared spectroscopy results suggested that the MPs did not break into smaller particles and they degrade directly into gaseous products. This work demonstrated that EO is a promising process for degradation of MPs in water without production of any wastes or by-products.