River-sea transition plays a key role in global geochemical cycles. The Yangtze River Estuary of China was selected as the research area, and the Section-Segmented Method was applied to determine the nutrient discharge from the Yangtze River to the East China Sea. A 3-D numerical model for the estuary was established and validated against the field investigated data. By numerical experiments the dynamics of hydrology and nutrient from 1950 to 2016 were simulated under four varied schemes. The individual and combined impacts on the nutrient flux induced by the Three-Gorges Dam (TGD) and the South-to-North Water Transfer Project (SNWTP) were explored. The following results were observed: (1) During the Pre-TGD period, the Yangtze River delivered the loads of 1.32 Tg/yr and 0.08 Tg/yr for TN and TP, respectively. July and Feb. were characterized by the highest and lowest monthly flux, respectively. (2) TGD played a significant role in regulating the temporal nutrient deliveries. After the closing of TGD, the discharges of TN and TP in the dry season respectively went up to 0.55 Tg and 0.032 Tg, with a mean increase of 28.3%. (3) SNWTP reduced the nutrient transport at a relatively stable level, and the total loads of 40.66 Gg and 2.4 Gg were reduced per year for TN and TP, respectively. (4) The combined impacts of TGD and SNWTP varied with seasons. October was characterized by the greatest cumulative effects. In dry seasons, the reduction caused by SNWTP was leveled by TGD-induced increase, limiting the flux variation linked to project operations.

Fluoxastrobin is one of the most widely used strobilurin fungicides, however, application of the fungicides may result in soil residues leading to environmental damage including oxidative stress and damage to sentinel organisms (i.e. earthworms). While this has been demonstrated in artificial soil, the biochemical response of Eisenia fetida exposed to fluoxastrobin in natural soils is unclear. This study utilized three typical natural soils (fluvo-aquic soils, red clay, and black soils) to evaluate the biochemical response of Eisenia fetida exposed to fluoxastrobin (0.1, 1.0, 2.5 mg/kg) including the production of reactive oxygen species, impact on three enzyme activities, lipid peroxidation, and 8-hydroxydeoxyguanosine after a 4-week exposure. The effects of fluoxastrobin on Eisenia fetida in different soils were assessed using an integrated biomarker response (IBR). The findings may be possible to state that the toxic effects of fluoxastrobin in artificial cannot exactly represent that in natural soils. Specifically, the fluoxastrobin subchronic toxicity was highest in red clay and lowest in black soil among the three natural soils. Furthermore, the 8-OHdG content was more sensitive to fluoxastrobin in all six environmental indicators of the present study.

Removal of dissolved sulfide contaminants from aqueous model solution using bio-derived porous graphitic carbon (PGC) impregnated with δ-MnO₂ was investigated. The composite adsorbent was synthesized using the chemical wet deposition method wherein MnO₂ was deposited on carbon walls through an in-situ reaction between permanganate and ethanol. Formation of transition metal oxide of manganese in the form of birnessite nanoparticles on interconnected PGC cell structure was confirmed by transmission electron microscopy, scanning electron microscopy, elemental analysis, and X-Ray diffraction characterization studies. The composite nanomaterial was tested for sulfide removal from aqueous solution at various conditions, including the pH, adsorbent dosage, initial solution concentration, and contact time. Adsorption results demonstrated an excellent adsorption capacity of ca. 90% within 20 min of contact time at 298 K. Equilibrium data collected from batch adsorption experiments fitted well with the Langmuir isotherm model (KL = 190 L/mg; R² = 0.99). The maximum adsorption capacity of the composite was estimated as 526.3 mg S²⁻/g at highly alkaline conditions compared to ca. 340 mg/g for a δ-MnO₂ adsorbent. Adsorptive oxidation of sulfides on composite MnO₂-PGC adsorbent was found to be controlled by the chemisorption process in accordance with the pseudo-second-order reaction model. Characterization of spent adsorbents revealed that sulfide was removed through adsorptive oxidation resulting in the formation of agglomerated particles of metal sulfate complexes and elemental sulfur. Analysis of reaction mechanism revealed that both MnO₂ and PGC played a role in the adsorptive oxidation of sulfides to CaSO₄ and elemental sulfur.

The plastic mulch films used in agriculture are considered to be a major source of the plastic residues found in soil. Mulching with low-density polyethylene (LDPE) is widely practiced and the resulting macro- and microscopic plastic residues in agricultural soil have aroused concerns for years. Over the past decades, a variety of biodegradable (Bio) plastics have been developed in the hope of reducing plastic contamination of the terrestrial ecosystem. However, the impact of these Bio plastics in agroecosystems have not been sufficiently studied. Therefore, we investigated the impact of macro (around 5 mm) and micro (<1 mm) sized plastic debris from LDPE and one type of starch-based Bio mulch film on soil physicochemical and hydrological properties. We used environmentally relevant concentrations of plastics, ranging from 0 to 2% (w/w), identified by field studies and literature review. We studied the effects of the plastic residue on a sandy soil for one month in a laboratory experiment. The bulk density, porosity, saturated hydraulic conductivity, field capacity and soil water repellency were altered significantly in the presence of the four kinds of plastic debris, while pH, electrical conductivity and aggregate stability were not substantially affected. Overall, our research provides clear experimental evidence that microplastics affect soil properties. The type, size and content of plastic debris as well as the interactions between these three factors played complex roles in the variations of the measured soil parameters. Living in a plastic era, it is crucial to conduct further interdisciplinary studies in order to have a comprehensive understanding of plastic debris in soil and agroecosystems.

A wide variety of sampling techniques and strategies are needed to analyze polycyclic aromatic compounds (PACs) and interpret their distributions in various environmental media (i.e., air, water, snow, soils, sediments, peat and biological material). In this review, we provide a summary of commonly employed sampling methods and strategies, as well as a discussion of routine and innovative approaches used to quantify and characterize PACs in frequently targeted environmental samples, with specific examples and applications in Canadian investigations. The pros and cons of different analytical techniques, including gas chromatography – flame ionization detection (GC-FID), GC low-resolution mass spectrometry (GC-LRMS), high performance liquid chromatography (HPLC) with ultraviolet, fluorescence or MS detection, GC high-resolution MS (GC-HRMS) and compound-specific stable (δ¹³C, δ²H) and radiocarbon (Δ¹⁴C) isotope analysis are considered. Using as an example research carried out in Canada’s Athabasca oil sands region (AOSR), where alkylated polycyclic aromatic hydrocarbons and sulfur-containing dibenzothiophenes are frequently targeted, the need to move beyond the standard list of sixteen EPA priority PAHs and for adoption of an AOSR bitumen PAC reference standard are highlighted.

Heat stress (HS) during gestation has been associated with negative outcomes, such as preterm birth or postnatal metabolic syndromes. The intestinal microbiota is a unique ecosystem playing an essential role in mediating the metabolism and health of mammals. Here we hypothesize late gestational HS alters maternal microbial transmission and structures offspring’s intestinal microbiota and serum metabolic profiles. Our results show maternal HS alters bacterial β-diversity and composition in sows and their piglets. In the maternal intestine, genera Ruminococcaceae UCG-005, [Eubacterium] coprostanoligenes group and Halomonas are higher by HS (q < 0.05), whereas the populations of Streptococcus, Bacteroidales RF16 group_norank and Roseburia are decreased (q < 0.05). In the maternal vagina, HS mainly elevates the proportions of phylum Bacteroidetes and Fusobacteria (q < 0.05), whereas reduces the population of Clostridiales Family XI (q < 0.05). In the neonatal intestine, maternal HS promotes the population of Proteobacteria but reduces the relative abundance of Firmicutes (q < 0.05). Moreover, the core Operational taxonomic units (OTU) analysis indicates the proportions of Clostridium sensu stricto 1, Romboutsia and Turicibacter are decreased by maternal HS in the intestinal and vaginal co-transmission, whereas that of phylum Proteobacteria and Epsilonbacteraeota, such as Escherichia-Shigella, Klebsiella, Acinetobacter, and Comamonas are increased in both the intestinal and vaginal co-transmission and the vagina. Additionally, Aeromonas is the only genus that is transmitted from environmental sources. Lastly, we evaluate the importance of neonatal differential OTU for the differential serum metabolites. The results indicate Acinetobacter significantly contributes to the differences in the adrenocorticotropic hormone (ACTH) and glucose levels due to HS (P < 0.05). Further, Stenotrophomonas is the most important variable for Cholesterol, low-density lipoprotein (LDL), diamine oxidase (DAO), blood urea nitrogen (BUN) and 5-hydroxytryptamine (5-HT) (P < 0.10). Overall, our data provides evidence for the maternal HS in establishing the neonatal microbiota via affecting maternal transmission, which in turn affects the maintenance of metabolic health.

Polycyclic aromatic hydrocarbons (PAHs) are a byproduct of combustion processes. They are common pollutants in oil-producing countries because fossil fuel processing generates PAHs that associate with dust. Airborne particles containing PAHs are transported into houses during dust storms, which are common in the arid oil-producing countries, and consequently the children and adults in the household are exposed to PAHs in indoor house dust. The goal of this study was to present a systematic survey of PAHs in indoor house dust in Kuwait. The PAHs concentrations and composition of indoor house dust was determined, along with their probable source and the potential carcinogenic risks. Total PAHs concentrations (ƩPAH) were, on average (±standard deviation) 1112 ± 347 μg/kg and ranged from 450 to 2242 μg/kg. Heavier congeners (4–6 ring PAHs) represented 61% of the ƩPAH. Petroleum combustion and traffic emissions were the major source of PAHs, based on the isomeric ratios of PAHs in indoor house dust. The incremental lifetime cancer risks (ILCRs) of exposure to PAHs in indoor house dust was 2.23 × 10⁻³ (95% CI: 1.99 × 10⁻³ – 2.48 × 10⁻³) for children and 2.15 × 10⁻³ (95% CI: 1.94 × 10⁻³ – 2.37 × 10⁻³) for adults, exceeding the US EPA safe limit of 1 × 10⁻⁶. Therefore, exposure to PAHs present in indoor house dust increases the cancer risk for children and adults in Kuwait.

Nonylphenol (NP) is a chemical raw material and intermediate which is mainly used in the production of surfactants, lubricating oil additives and pesticide emulsifiers. NP is reported to be toxic on the immune system, nervous system and reproductive system due to its binding to estrogen receptors. However, the toxicity of NP on mammalian oocyte quality remains unclear. In present study, we explored the effects of NP exposure on mouse oocyte maturation. Our results showed that 4 weeks of NP exposure increased the number of atresia follicles and decreased oocyte developmental competence. Transcriptomic analysis indicated that NP exposure altered the expression of more than 800 genes in oocytes, including multiple biological pathways. Subcellular structure examination indicated that NP exposure disrupted meiotic spindle organization and caused chromosome misalignment. Moreover, aberrant mitochondrial distribution and decreased membrane potential were also observed, indicating that NP exposure caused mitochondria dysfunction. Further analysis showed that NP exposure resulted in the accumulation of reactive oxygen species (ROS), which causes oxidative stress; and the NP-exposed oocytes showed positive Annexin-V signal, indicating the occurrence of early apoptosis. In summary, our results indicated that NP exposure reduced oocyte quality by affecting cytoskeletal dynamics and mitochondrial function, which further induced oxidative stress and apoptosis in mice.

As the most important gas-phase alkaline species, atmospheric ammonia (NH3) contributes considerably to the formation and development of fine-mode particles (PM2.5), which affect air quality and environmental health. Recent satellite-based observations suggest that the North China Plain is the largest agricultural NH3 emission source in China. However, our isotopic approach shows that the surface NH3 in the intraregional urban environment of Beijing-Tianjin-Shijiazhuang is contributed primarily by combustion-related processes (i.e., coal combustion, NH3 slip, and vehicle exhaust). Specifically, the Batch fractionation model was used to describe the partitioning of gaseous NH3 into particles and to trace the near-ground atmospheric NH3 sources. With the development of haze pollution, the dynamics of δ15N-NH4+ were generally consistent with the fractionation model. The simulated initial δ15N-NH3 values ranged from −22.6‰ to −2.1‰, suggesting the dominance of combustion-related sources for urban NH3. These emission sources contributed significantly (92% on hazy days and 67% on clean days) to the total ambient NH3 in urban cities, as indicated by a Bayesian mixing model. Based on the Batch fractionation model, we concluded the following: 1) δ15N-NH4+ can be used to model the evolution of fine-mode aerosols and 2) combustion-related sources dominate the near-ground atmospheric NH3 in urban cities. These findings highlight the need for regulatory controls on gaseous NH3 emissions transported from local and surrounding industrial sources.

Ozone has become a major atmospheric pollutant in China as the pattern of urban energy usage has changed and the number of motor vehicles has grown rapidly. The Beijing-Tianjin-Hebei Urban Agglomeration, also known as the Jing-Jin-Ji Urban Agglomeration (hereafter, JJJUA), with a precarious balance between protecting the ecological environment and sustaining economic development, is challenged by high levels of ozone pollution. Based on ozone observation data from 13 cities in the JJJUA from 2014 to 2017, the spatio-temporal trends in the evolution of ozone pollution and its associated influencing factors were analyzed using Moran’s I Index, hot-spot analysis, and Geodetector using ArcGIS and SPSS software. Five key results were obtained. 1) There was an increase in the annual average ozone concentration, for the period 2014–2017. Comparing the 13 prefecture-level cities, ozone pollution in Chengde and Hengshui decreased, while it worsened in the remaining 11 cities. 2) Ozone pollution was worse in spring and summer than in autumn and winter; the peak ozone pollution season was from May to September; the average ozone concentration on workdays was higher than that on non-workdays, showing a counter-weekend effect. 3) Annual average concentrations were high in the central and southern parts of the study region but low in the north. 4) Prominent positive spatial correlations were observed in ozone concentration, with the best correlations shown in summer and autumn; concentrations were high in Baoding and Xingtai but low in Beijing and Chengde. 5) Concentrations of PM10, NO2, CO, SO2, and PM2.5, as well as average wind speed, sunshine duration, evaporation, precipitation, and temperature, all had significant effects on ozone pollution, and interactions between these influencing factors increased it.