Nitrogen contamination is a global concern and has been a serious problem in agricultural areas. The present study was carried out in an intensively irrigated region of northwest China along the New Silk Road, Yinchuan Plain, where the residents depend on the groundwater as the primary source for drinking. To understand the nitrogen contamination in the aquifer system, the distribution of nitrate and ammonium and its controlling factors were studied based on hydrochemical, hydrogeological, and isotopic analyses. 11.37 and 40% of phreatic water samples are categorized as NO₃–N and NH₄–N pollution in accordance with the WHO standards. A total of 59.52% of confined water samples has high NH₄–N values, exceeding the permissible limit for drinking purpose. The results indicate NO₃–N predominates in the shallow water and NH₄–N predominates in the deep water for the single phreatic aquifer. For the multilayer structure area, NO₃–N predominates in the phreatic aquifer of the western and the southern parts of the plain; NH₄–N predominates in the phreatic aquifer of the middle and the northern parts of the plain, and in the confined aquifers where groundwater pumping had been performed. The mixture of synthetic fertilizer and manure/sewage is primarily responsible for the phreatic water based on isotopic analysis. In the confined aquifers, higher NH₄–N concentrations are mainly attributed to intensive pumping under higher pumping rates. The results of this study can be used as a scientific basis for the future research on nitrogen in the plain. They can also be used by scholars and decision makers who are interested in groundwater protection and sustainable development.

A chemical-activated carbon (CAC) was prepared by phosphoric acid activation of olive stone. The CAC was characterized using various analytical techniques and evaluated for the removal of amoxicillin from aqueous solutions under different operating conditions (initial concentration, 12.5–100 mg L⁻¹, temperature, 20–25 °C, contact time, 0–7000 min). The CAC characterization indicates that it is a microporous carbon with a specific surface area of 1174 m²/g and a pore volume of 0.46 cm³/g and contains essentially acidic functional groups. The adsorption tests indicated that 93 % of amoxicillin was removed at 20 °C for 25 mg L⁻¹ initial concentration. Moreover, it was found that adsorption capacity increased with contact time and temperature. Kinetic study shows that the highest correlation was obtained for the pseudo-second-order kinetic model, which confirms that the process of adsorption of amoxicillin is mainly chemisorption. Using the intraparticle diffusion model, the mechanism of the adsorption process was determined. The equilibrium data analysis showed that the Sips and Langmuir models fitted well the experimental data with maximal adsorption capacities of 67.7 and 57 mg/g, respectively, at 25 °C. The chemical-activated carbon of olive stones could be considered as an efficient adsorbent for amoxicillin removal from aqueous solutions.

Because of the harmful effects of greenhouse gas (GHG) emitted by petroleum-based fuels, the adoption of alternative green fuels such as biodiesel and compressed natural gas (CNG) is an inevitable trend in the transportation sector. However, the transition to alternative fuel vehicle (AFV) fleets is not easy and, particularly at the beginning of the transition period, drivers may be forced to travel long distances to reach alternative fueling stations (AFSs). In this paper, the utilization of bi-fuel vehicles is proposed as an operational approach. We present a mathematical model to address vehicle routing problem (VRP) with bi-fuel vehicles and show that the utilization of bi-fuel vehicles can lead to a significant reduction in GHG emissions. Moreover, a simulated annealing algorithm is adopted to solve large instances of this problem. The performance of the proposed algorithm is evaluated on some random instances.

Modern, efficient, and cost-effective approach to remediation of heavy metal-contaminated soil is based on the application of microorganisms. In this paper, four isolates from agricultural and urban contaminated soil showed abundant growth in the presence of copper(II) sulfate pentahydrate (CuSO₄·5H₂O) up to 2 mM. Selected yeasts were identified by molecular methods as Candida tropicalis (three isolates) and Schwanniomyces occidentalis (one isolate). C. tropicalis (4TD1101S) showed the highest percentage of bioaccumulation capabilities (94.37%), determined by the inductively coupled plasma optical emission spectrometry (ICP-OES). The Raman spectra of C. tropicalis (4TD1101S) analyzed in a medium with the addition of 2 mM CuSO₄·5H₂O showed certain increase in metallothionein production, which represents a specific response of the yeast species to the stress conditions. These results indicate that soil yeasts represent a potential for practical application in the bioremediation of contaminated environments.

The use of the lipophilic persistent organic pollutants (POPs) including polychlorinated biphenyls (PCBs) and several organochlorine pesticides (OCPs) has been prohibited for more than 30 years. In this study, we present the temporal trends of the lipophilic POP serum concentrations in Danish nulliparous pregnant women between 2011 and 2013. We randomly selected 197 pregnant women (gestational age 11–13) from the Aarhus Birth Cohort. The concentrations of the lipophilic POPs in the serum samples were analyzed using gas chromatography. The concentrations were corrected for total serum lipids. The statistical analysis was performed by regression analysis with adjustment for age, BMI, gestational age at blood draw, and smoking status. The serum concentrations of PCB 118, 138, 153, 156, 170, 180, 187, and hexachlorobenzen, trans-nonachlor, β-hexachlorocyclohexane (β-HCH), and p,p’-dichlorodiphenyldichloroethylene were lower in 2013 than in 2011. However, the oxychlordane concentration was lowest in 2011. The serum levels of most lipophilic POPs followed downward trends during the study period, which was expected, as these compounds has been banned for many years. The upward trend of oxychlordane was unexpected and presumably a chance finding.

Groundwater quality in bone-dry and semiarid areas of Iran is decreasing because of contaminants from natural origins and anthropogenic sources. Among many harmful contaminants, nitrate and fluoride ions are more common. This study was carried out with the aim of determining geochemical processes controlling chemistry of groundwater with special reference to nitrate and fluoride enrichment in groundwater in Lar plain aquifer, south of Iran. Groundwater samples were collected from 17 sites and analyzed for main constituents (Na, K, Ca, Mg, Cl, SO₄ ²⁻, HCO₃ ⁻, F⁻, and NO₃ ⁻). Composite diagram, saturation indices calculation, and multivariate analysis techniques including cluster and factor analyses were employed in evaluating groundwater quality. The EC ranges from 8793.87 to 13,345.00 μS/cm in wet season and from 9621.59 to 12,640.00 μS/cm in dry season. Fluoride amounts range between 0.59 and 3.92 mg/L. Nitrate concentrations range between 1.47 and 70.66 mg/L. Results indicate that dissolution–precipitation of carbonate and evaporate minerals, evaporation (in terms of agricultural water return), and opposite ion interchange are the main processes that determine groundwater chemistry. It seems that fluoride has a natural origin and the equilibrium reaction between fluorite and calcite is very significant to control fluoride concentration level in water. Vertical variation of nitrate concentration and distribution of agricultural areas have indicated that nitrate originated from nitrogenous inorganic fertilizers used during irrigation periods. The results also indicate that denitrification takes place in the aquifer and that nitrate decline is not only a function of dilution but also a process of denitrification.

The research objective has been to evaluate the effect, unexplored yet, of a mixture of three active ingredients of the herbicide Lumax 537.5 SE: terbuthylazine (T), mesotrione (M), and S-metolachlor (S) on counts of soil microorganisms, structure of microbial communities, activity of soil enzymes as well as the growth and development of maize. The research was based on a pot experiment established on sandy soil with pHKCₗ 7.0. The herbicide was applied to soil once, in the form of liquid emulsion dosed as follows: 0.67, 13.4, 26.9, 53.8, 108, 215, and 430 mg kg⁻¹ of soil, converted per active substance (M + T + S). The control sample consisted of soil untreated with herbicide. The results showed that the mixture of the above active substances caused changes in values of the colony development (CD) indices of organotrophic bacteria, actinomycetes, and fungi and ecophysiological diversity (EP) indices of fungi. Changes in the ecophysiological diversity index of organotrophic bacteria and actinomycetes were small. The M + T + S mixture was a strong inhibitor of dehydrogenases, to a less degree catalase, urease, β-glucosidase, and arylsulfatase, while being a weak inhibitor of phosphatases. The actual impact was correlated with the dosage. The M + T + S mixture inhibited the growth and development of maize. The herbicide Lumax 537.5 SE should be applied strictly in line with the regime that defines its optimum dosage. Should its application adhere to the manufacturer’s instructions, the herbicide would not cause any serious disturbance in soil homeostasis. However, its excessive quantities (from 13.442 to 430.144 mg kg⁻¹ DM of soil) proved to be harmful to the soil environment.

The environmental impacts of various pollutants on the entire levels of organisms are under investigation. Among these pollutants, endocrine-disrupting compounds (EDCs) present a serious hazard, even though the environmental significance of these compounds remains basically unknown. To drop some light on this field, we assessed the effects of a 11-day exposure of 17α-ethinylestradiol (EE2) on the growth, metabolic content, antioxidant response, oxidative stress, and genetic damage of Dunaliella salina, isolated from Tunisian biotopes. The results showed that at 10 ng L⁻¹, EE2 could stimulate the growth of D. salina and increase its cellular content of photosynthetic pigments and metabolites; however, it did not significantly increase the activities of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx) or the level of malondialdehyde (MDA) and hydrogen peroxide (H₂O₂). In contrast, exposure to high levels of EE2 concentrations significantly inhibited the growth of D. salina (P < 0.05), decreased the cellular content of photosynthetic pigments, increased the cellular content of all of the metabolites and the SOD activity, and inhibited CAT and GPx activities. Nevertheless, the balance between oxidant and antioxidant enzymes was disrupted because H₂O₂ content along with MDA content simultaneously increased. Contrary to expected results, DNA damage (strand breaks) decreased after the exposure of algae to EE2. The results of this study suggest that EE2 toxicity could result in environmental impacts with consequences on the whole aquatic community. Graphical abstract

High-level black carbon (BC) pollution is associated with traffic emissions in metropolitan areas with high vehicle density. Mobile monitoring was conducted to assess the in-vehicle BC exposure on three backbone ring roads (inner, middle, and outer ring roads) on October 14 and October 18, 2015 in Shanghai. Ambient BC monitoring was also simultaneously conducted in three fixed roadside stations from October 14 to October 20, 2015. Results of the mobile monitoring showed median BC personal exposure concentrations ranging from 5.0 μg m⁻³ on the inner ring road to 13.5 μg m⁻³ on the outer ring road. The ambient BC concentrations during the entire observation period showed an arithmetic mean and a standard deviation of 3.5 ± 2.9 μg m⁻³. The correlation analysis of urban roadside monitoring (Caoxi Road and South Zhongshan Road) and personal data showed a high and significant correlation. The results of this study highlight the critical level of BC pollution in Shanghai and facilitate the development of evidence-based public health interventions and control strategies to prevent the adverse health effects of BC pollution.

The oxidation of chloramphenicol (CAP) by potassium ferrate (VI) in test solution was studied in this paper. A series of jar tests were performed at bench scale with pH of 5–9 and molar ratio [VI/CAP] of 16.3:1–81.6:1. Results showed that raising VI dose could improve the treatment performance and the influence of solution pH was significant. VI is more reactive in neutral conditions, presenting the highest removal efficiency of CAP. The rate law for the oxidation of CAP by VI was first order with respect to each reactant, yielding an overall second-order reaction. Furthermore, five oxidation products were observed during CAP oxidation by VI. Results revealed that VI attacked the amide group of CAP, leading to the cleavage of the group, while benzene ring remained intact.