Zinc nanoparticles were synthesized using aqueous leaf extract of Justicia adhatoda L. The characterization of nanoparticles was done by ultraviolet-visible (UV-vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), and high-resolution transmission electron microscopy (HR-TEM). The characteristic absorption peak of the UV spectrum was recorded at 379 nm. The FTIR data revealed the possible biomolecules involved in bioreduction and capping of zinc nanoparticles for efficient stabilization. AFM and HR-TEM images have shown that the size of zinc nanoparticles ranges from 55 to 83 nm and they are spherical in shape. The biogenic zinc nanoparticles were evaluated for their toxic effect on mitotic chromosomes of Allium cepa as a model system. Experiments were conducted in triplicate to assay the effect of 25, 50, 75, and 100 % of zinc nanoparticles on mitotic chromosomes at an interval of 6 h duration for 24 h. The investigation revealed that the mitotic index (MI) was decreased with increased concentration of zinc nanoparticles and exposure duration. The results revealed that zinc nanoparticles have induced abnormalities like anaphase bridge formation, diagonal anaphase, C-metaphase, sticky metaphase, laggards, and sticky anaphase at different percentages and times of exposure. It is evident from the observation that mitotic cell division becomes abortive at 100 % treatment of zinc nanoparticles.

China has been confronted with serious water quality deterioration concurrent with rapid socioeconomic progress during the past 40 years. Consequently, knowledge about economic growth and lake water quality dynamics is important to understand eutrophication processes. Objectives were to (i) reconstruct historical nutrient accumulation and the basin economic progress on burial flux (BF); (ii) determine forms and structures of nitrogen (N) and phosphorus (P) in sediment and water using six cores in three of the most severely eutrophic lake areas in China (i.e., Eastern Plain, Yunnan-Guizhou Plain, and Inner Mongolia–Xinjiang regions). Results suggest that BFs of total nitrogen (TN) continued to increase in sediment, whereas total phosphorus (TP) levels were consistent or only slightly increased, except in highly polluted lakes during the past decades. Similar results were observed for concentrations of nutrients in water (i.e., increased N/P). This historical distribution pattern was correlated to long-term fertilization practices of farmers in the watershed (N fertilization exceeds that of P) and was contingent upon pollution control policies (e.g., emphasized P whereas N was ignored). Vertical profiles of BFs indicated that lake nutrient accumulation included three stages in China. Nutrient accumulation started in the 1980s, accelerated from the 1990s, and then declined after 2000. Before the 1980s, nutrients were relatively low and stable, with nutrient inputs being controlled by natural processes. Thereafter, N- and P-bound sediments dramatically increased due to the increasing influence of anthropogenic processes. Nutrients were primarily derived from industries and domestic sewage. After 2000, BFs of nutrients were steady and even decreased, owing to implementation of watershed load reduction policies. The decreasing NaOH-extracted P (Fe/Al–P) and increasing organic phosphorus (OP) indicated that the source of exogenous pollution underwent a shift. Inputs of nutrients were predominantly from agricultural and domestic sewage, whereas industrial pollution has been gradually controlled in most of the watersheds. Historical nutrient dynamics suggest that the economy of China is growing at the expense of its aquatic ecological environments. Therefore, more attention to nutrient export to groundwater resulting from economic development is important for further aquatic ecosystem deterioration and eutrophication in China.

The choice of substrates with high adsorption capacity, yet readily available and economical is vital for sustainable pollutants removal in constructed wetlands (CWs). Two identical large-scale demonstration horizontal subsurface flow (HSSF) CWs (surface area, 340 m²; depth, 0.6 m; HLR, 0.2 m/day) with gravel or slag substrates were evaluated for their potential use in remediating polluted urban river water in the prevailing climate of northwest China. Batch experiments to elucidate phosphorus adsorption mechanisms indicated a higher adsorption capacity of slag (3.15 g/kg) than gravel (0.81 g/kg), whereby circa 20 % more total phosphorus (TP) removal was recorded in HSSF-slag than HSSF-gravel. TP removal occurred predominantly via CaO-slag dissolution followed by Ca phosphate precipitation. Moreover, average removals of chemical oxygen demand and biochemical oxygen demand were approximately 10 % higher in HSSF-slag than HSSF-gravel. Nevertheless, TP adsorption by slag seemed to get quickly saturated over the monitoring period, and the removal efficiency of the HSSF-slag approached that of the HSSF-gravel after 1-year continuous operation. In contrast, the two CWs achieved similar nitrogen removal during the 2-year monitoring period. Findings also indicated that gravel provided better support for the development of other wetland components such as biomass, whereby the biomass production and the amount of total nitrogen (TN; 43.1–59.0 g/m²) and TP (4.15–5.75 g/m²) assimilated by local Phragmites australis in HSSF-gravel were higher than that in HSSF-slag (41.2–52.0 g/m² and 3.96–4.07 g/m², respectively). Overall, comparable pollutant removal rates could be achieved in large-scale HSSF CWs with either gravel or slag as substrate and provide a possible solution for polluted urban river remediation in northern China.

The underground extraction of Pb-Zn mineralization in the Touiref area stopped in 1958. A large volume of flotation tailings (more than 500 Mt) containing sulfides were deposited in a tailings impoundment. The goals of this study are to evaluate the neutralization capacity of the unoxidized and oxidized tailings, to assess the speciation of metals between the different components of the tailings material, and to assess the mobility of metals and the secondary minerals’ precipitation in pore waters using geochemical modeling. To accomplish these objectives, representative samples from both fresh and oxidized zones were collected along a vertical profile through the tailings pile. Physical, chemical (ICP-MS), and mineralogical characterization (X-ray diffraction (XRD), reflected light microscopy, scanning electron microscope (SEM)) of these samples was performed. Grain size analysis shows that the tailings are dominated by silt- to sand-sized fractions. The microscopic observation highlights the presence of pyrite, marcasite, galena, and sphalerite as primary minerals in a carbonated matrix. The study reveals also the presence of secondary minerals represented by cerussite, smithsonite, anglesite, and Fe oxi-hydroxides as important scavengers for trace elements. The static tests show that the presence of calcite in the tailing samples ensures acid-neutralizing capacity (ANC), which is significantly greater than the acidity potential (PA). The geochemical characterization of the unoxidized samples shows higher Cd, Pb, and Zn concentrations than the oxidized samples containing the highest values for Fe and SO₄. Sequential extraction tests show that significant percentages of metals are distributed between the acid-soluble fractions (Cd, Pb, and Zn) and the reducible one (Zn). Pore water analysis indicates that Ca is the dominant cation (8,170 and 6,200 mg L⁻¹, respectively), whereas sulfate is the principal anion (6,900 and 5,100 mg L⁻¹, respectively). Saturation index (SI) calculations of minerals in pore water extracted from both the oxidized and unoxidized samples are indicative of gypsum (SI >0) and Fe(III) oxides (SI ≫0) precipitation. The latter controls the Fe concentration in solution.

The aim of this study was to examine the hypothesis that organochlorine pesticides (OCPs), hexachlorobenzene (HCB), β-hexachlorocyclohexane (β-HCH), and 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (p,p′-DDT) and its metabolite 1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene (p,p′- DDE) are ototoxic to humans. A multivariate general linear model was designed, in which the statistical relation between blood serum concentrations of HCB, β-HCH, p,p′-DDT, or p,p′-DDE at different ages (at birth, 6, 16, and 45 months) and the distortion product otoacoustic emissions (DPOAEs) was treated as multivariate outcome variables. Polychlorinated biphenyl (PCB) congeners and OCPs were strongly correlated in serum of children from our cohort. To ascertain that the association between DPOAEs at a given frequency and concentration of a pesticide is not influenced by PCBs or other OCP also present in serum, we calculated benchmark concentrations (BMCs) relating DPOAEs to a serum pesticide alone and in presence of confounding PCB-153 or other OCPs. We found that BMCs relating DPOAEs to serum pesticides are not affected by confounders. DPOAE amplitudes were associated with serum OCPs at all investigated time intervals, however, in a positive way with prenatal exposure and in a negative way with all postnatal exposures. We observed tonotopicity in the association of pesticides with amplitude of DPOAEs as its strength was frequency dependent. We conclude that exposure to OCPs in infancy at environmental concentrations may be associated with hearing deficits.

We evaluated concentrations of 15 PCB congeners in blood serum of 2047 adults, 431 8–9-year old children and 1134 mother-child pairs born in 2001–2003. These subjects were long-standing residents living up to 70 km (to the north) and up to 50 km (to the south) of the former Chemko Strážske PCB production facility in the Michalovce district of Slovakia. We plotted serum concentration against distance from the plant both with and without consideration of the direction of their homes from the site. The decrease in exposure with distance could be described by an exponential function which was dependent on direction and climatic parameters. By kriging we created maps depicting predicted isoconcentration contours for sex- and age-adjusted serum concentration of ∑PCBs for the same group of children, adults and mothers. The principle of our risk analysis was to relate serum concentration data, reflecting PCB body burden, using the critical concentrations established by the French Agency for Food, Environmental and Occupational Health & Safety (ANSES 2010) as thresholds below which the probability of effects on health is regarded as negligible. We conclude that 10 years ago, around 200,000 residents were at risk in this densely populated area. Exposure has since decreased but the mechanism for this has not yet been studied.

Lead emissions originate primarily from the anthropogenic lead cycle, and research into their characteristics, such as species type, provides essential information for pollution control. A dynamic model for global lead emissions has been established, and their emissions and temporal accumulations were estimated in this study based on the evolution of the lead cycle over 70 years. An inventory of the emissions species was obtained after identifying their physiochemical transformations. The 2010 emissions were 3.56 Mt, with 65 % coming from waste management and recycling. The main species were PbSO₄(42.5 %), PbO₂(16.2 %), and PbS (8.3 %). Between 1930 and 2010, the total lead emissions were 173.8 Mt, mainly from waste management and recycling (48 %), production (26 %), and use (20 %). The main species were PbSO₄, PbO, Pb, and PbS, and together, they accounted for 61.2 % of the total emissions. Over time, species, such as tetraethyl lead and Pb, declined, but PbO₂and PbSO₄increased.

The chemical characterization of particulate matter (PM) 2.5 fraction was studied during a 1-year sampling campaign conducted at a site near Thessaloniki’s port area. PM2.5 collected samples were chemically analyzed for polycyclic aromatic hydrocarbons, minerals, and trace elements (Pb, Ni, Cu, V, Mn, Cr, Zn, Mg, K, Ti, Fe, Ca, and Al); water-soluble ions (Cl⁻, NO₃⁻, SO₄²⁻, K⁺, Na⁺, NH₄⁺, Mg²⁺, Ca²⁺); and organic and elemental carbon. The average annual PM2.5 concentration (66.0 μg/m³) was at the highest level compared with other studies reported for the same city but different sampling sites. The average daily sum of the measured concentration of polycyclic aromatic hydrocarbons (PAHs) was 12.76 ng/m³; this value decreased to 6.73 ng/m³for the warm period and reached the value of 19.8 ng/m³for the cold period. The average concentration of benzo[a]pyrene during the sampling period was 0.75 ng/m³, which is below the European Union limit value of 1.0 ng/m³. The ionic content comprised, on average, 22.6 % of the PM2.5 mass, with sulfate and ammonium being the most abundant species (31 and 26 %, respectively, of measured ions during the whole sampling period). The annual mean concentrations of organic carbon (OC) and elemental carbon (EC) were 10.5 ± 6.3 and 2.3 ± 1.5 μg/m³, respectively. The OC/EC ratio ranged from 1.6 to 9.9, suggesting that there is a significant influence of residential wood burning for heating as well as ship and vehicle emissions to the sampling area. Finally, the elemental composition of associated PM2.5 was dominated by Ca, Fe, and Al. Although conclusions based only on PM2.5 measurements cannot entirely estimate all harbor sources’ contribution, there is evidence to support that port activities affect the city’s air quality and vice versa.

This study was launched to establish comprehensive environmental monitoring on the levels and patterns of polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), and polycyclic aromatic hydrocarbons (PAHs) both in soil and ambient air around a thermal desorption plant in China. All 209 congeners of PCBs, 136 congeners of PCDD/Fs (P = 4 to 8) and 16 EPA priority PAHs were analyzed. The concentration of PCBs ranged from 20.0 to 536 ng g⁻¹(or 0.077–5.27 pg WHO-TEQ g⁻¹) in soil and from 972 to 991 ng Nm⁻³(or 0.245–0.374 pg WHO-TEQ Nm⁻³) in air samples, much higher than the levels in cities. A single soil sampling point could have been affected by some transfer of PCBs from the untreated soil by the fingerprint characteristics and the statistical analysis. Establishing blank values prior to the start-up of new plant is a safe and sure method to establish subsequent impacts on the environment. During the treatment of hazardous waste, strict control of all waste materials and all emissions is required.

Bi₂MoO₆oxide was synthesized by hydrothermal reaction in the presence of EDTA under different experimental conditions (time of reaction and EDTA concentration) in order to obtain materials with specific textural properties. It was determined that the addition of EDTA influences the final physical properties of Bi₂MoO₆. The photocatalytic activity of Bi₂MoO₆samples was evaluated in the degradation reaction of indigo carmine (IC) in aqueous solution under solar radiation type. The best results as photocatalyst were obtained with the sample hydrothermally synthesized at 150 ºC for 4h in presence of a 0.031 M EDTA solution. This sample was able to whiten a solution of IC in a 94% after 120 min of lamp irradiation with t₁/₂ = 31 min. In general, the samples prepared with lower concentrations of EDTA were the best photocatalysts. A gradual decrease in the activity was observed in the samples prepared with the same EDTA concentration as was increased in the reaction time. Beyond differences in morphology and textural properties of the samples prepared, the presence of EDTA by-products on the samples and the decomposition degree of it were important factors in determining the activity of the photocatalysts. Analysis of total organic carbon (TOC) of samples irradiated for 100 h confirmed that Bi₂MoO₆oxide is able to mineralize the complex organic molecule of IC to CO₂and H₂O in 55 %.