Nutrient recovery from human urine is a promising pretreatment of domestic wastewater and provides a sustainable recyclability of N and P. In this study, batch experiments were conducted to identify the characteristics of natural loess (NL) for the adsorption and recovery of ammonium and phosphate from hydrolysis urine (HU). The adsorption mechanisms, the adsorption kinetics and isotherms, as well as the major influencing factors, such as pH and temperature, were investigated. Results revealed that adsorption of ammonium occurred by means of ion exchange and molecule adsorption with the ≡Si–OH groups, while phosphate adsorption was based on the calcium phosphate precipitation reaction and formation of inner-sphere complexes with ≡ M–OH groups. The adsorption processes of ammonium and phosphate were well described by the pseudo-second-order kinetic model and the Freundlich isotherm model. Adsorption of phosphate was endothermic, while ammonium adsorption was exothermic. Furthermore, the maximum ammonium and phosphate adsorption capacities of NL was 23.24 mg N g–¹ and 4.01 mg P g–¹ at an initial pH of 9 and 10, respectively. Results demonstrated that nutrient-adsorbed NL used as compound fertilizer or conventional fertilizer superaddition was feasible for its high contents of N and P as well as its environmental friendliness.

Lanthanum-modified bentonite has potential for wide application in eutrophication control. We investigated P adsorption on a lanthanum-modified bentonite by analysis of adsorption kinetics, equilibrium, and the effect of environmental factors. P adsorption closely followed the pseudo-second-order kinetic model, and the isotherm was well described by the Langmuir model. This adsorbent could effectively immobilize P into the sediment, but the adsorption process was strongly dependent on pH, anions, and low molecular weight organic acids (LMWOAs). P adsorption increased with increasing pH from 0.52 mg P/g at pH 3.0 to 0.93 mg P/g at pH 7.0 with no adsorption at pH 11. P adsorption was strongly inhibited in the presence of anions and three LMWOAs, with P even re-released at high concentrations. These environmental factors should be given significant attention when considering the application of lanthanum-modified bentonite in eutrophication control.

A field investigation of contaminant transport beneath and around an uncontrolled landfill site in Huainan in China is presented in this paper. The research aimed at studying the migration of some chemicals present in the landfill leachate into the surrounding clayey soils after 17 years of landfill operation. The concentrations of chloride and sodium ions in the pore water of soil samples collected at depths up to 15 m were obtained through an extensive site investigation. The contents of organic matter in the soil samples were also determined. A two-dimensional numerical study of the reactive transport of sodium and chloride ion in the soil strata beneath and outside the landfill is also presented. The numerical modelling approach adopted is based on finite element/finite difference techniques. The domain size of approximately 300 × 30 m has been analysed and major chemical transport parameters/mechanisms are established via a series of calibration exercises. Numerical simulations were then performed to predict the long-term behaviour of the landfill in relation to the chemicals studied. The lateral migration distance of the chloride ions was more than 40 m which indicates that the advection and mechanical dispersion are the dominant mechanism controlling the contaminant transport at this site. The results obtained from the analysis of chloride and sodium migration also indicated a non-uniform advective flow regime of ions with depth, which were localised in the first few metres of the soil beneath the disposal site. The results of long-term simulations of contaminant transport indicated that the concentrations of ions can be 10 to 30 times larger than that related to the allowable limit of concentration values. The results of this study may be of application and interest in the assessment of potential groundwater and soil contamination at this site with a late Pleistocene clayey soil. The obtained transport properties of the soils and the contaminant transport mechanisms can also be used for the design of engineered barriers for the control of the long-term pollution of the site.

PM10 and black smoke were monitored at a suburban sampling station located in the northern Spanish city of Gijón. Thirty-two metals and total carbon (TC) (i.e., organic carbon (OC) and elemental carbon (EC)) were analyzed over a year. The study of air-mass origin based on 5-day back trajectories was carried out to assess its influence on the recovery data. Different strategies were implemented to infer the influence of traffic in the area. On average, TC accounted for 29 % of the PM10 fraction, with OC forming 77 % of this TC. The influence of traffic was clearly reduced during intense Atlantic advection episodes, when OC and EC decreased up to 0.39 and 0.22 μg C/m³, respectively. In contrast, the highest values were reported during regional episodes, exceeding 10 μg C/m³ of OC and 2 μg C/m³ of EC. The correlation between EC and OC was found to notably improve when considering the days with high traffic flow (from R ² = 0.46 to R ² = 0.74). This pattern was also reproduced by black smoke and EC (from R ² = 0.49 to R ² = 0.59). Cu and Sn were found to be reliable traffic tracers given their high dependence on EC (R ² = 0.82 and R ² = 0.79, respectively). Nevertheless, Sn, Ba, and Sb showed a better correlation with Cu than EC, suggesting a common origin. In the case of Sn, R ² improved from 0.79 to 0.91. The Cu/Sb ratio had a mean value of 6.6 which agrees with diagnostic criterions for brake wear particles. The relationships and ratios between EC, Cu, Sb, Sn, Ba, and Bi pointed out to non-exhaust emissions, playing a significant role in the chemical composition of PM10. Brake wear was presented as the most likely origin for Cu, Sb, and Sn.

Uniform 2-year old seedlings of a commercial olive cultivar (Olea europaea L., cv. Mahzam) were exposed or unexposed to the air pollution from the controlled burning of waste tires. The plants were supplied with zinc sulfate (ZnSO₄) or synthesized Zn(Glycine)₂ (Zn-Gly) or unsupplied with Zn. Exposure to air pollution resulted in oxidative damage to the olive, as indicated by the higher production of malondialdehyde (MDA). Supplement with Zn partly alleviated oxidative damage induced by the air emissions on the olive. Leaf concentration of MDA was higher at the active period of tire burning than that of the inactive one. Exposure to the emissions from tire burning significantly increased leaf ascorbate peroxidase (APX) activity. Supplement with Zn increased APX activity in plants exposed to the air pollution. According to the results, Zn nutrition was effective in alleviating oxidative stress induced by air pollution on the olive. APX seemed to play a significant role in alleviating oxidative damages induced by air emissions from tire burning on the olive; however, the role of other antioxidant enzymes should be addressed in future studies.

Commercial production of nanoparticles (NP) has created a need for research to support regulation of nanotechnology. In the current study, microbial biofilm communities were developed in rotating annular reactors during continuous exposure to 500 μg L⁻¹ of each nanomaterial and subjected to multimetric analyses. Scanning transmission X-ray spectromicroscopy (STXM) was used to detect and estimate the presence of the carbon nanomaterials in the biofilm communities. Microscopy observations indicated that the communities were visibly different in appearance with changes in abundance of filamentous cyanobacteria in particular. Microscale analyses indicated that fullerene (C60) did not significantly (p < 0.05) impact algal, cyanobacterial or bacterial biomass. In contrast, MWCNT exposure resulted in a significant decline in algal and bacteria biomass. Interestingly, the presence of SWCNT products increased algal biomass, significantly in the case of SWCNT-COOH (p < 0.05) but had no significant impact on cyanobacterial or bacterial biomass. Thymidine incorporation indicated that bacterial production was significantly reduced (p < 0.05) by all nanomaterials with the exception of fullerene. Biolog assessment of carbon utilization revealed few significant effects with the exception of the utilization of carboxylic acids. PCA and ANOSIM analyses of denaturing gradient gel electrophoresis (DGGE) results indicated that the bacterial communities exposed to fullerene were not different from the control, the MWCNT and SWNT-OH differed from the control but not each other, whereas the SWCNT and SWCNT-COOH both differed from all other treatments and were significantly different from the control (p < 0.05). Fluorescent lectin binding analyses also indicated significant (p < 0.05) changes in the nature and quantities of exopolymer consistent with changes in microbial community structure during exposure to all nanomaterials. Enumeration of protozoan grazers showed declines in communities exposed to fullerene or MWCNT but a trend for increases in all SWCNT exposures. Observations indicated that at 500 μg L⁻¹, carbon nanomaterials significantly alter aspects of microbial community structure and function supporting the need for further evaluation of their effects in aquatic habitats.

This work focuses on the exposure of maize plants to nanomolar concentrations of Cd, which is relevant for agricultural soils cropped with food and feed plants. Maize plants were cultivated in nutrient solution at 0.8 or 20 nM Cd during the vegetative growth stages. No significant hormesis or toxic effects of Cd were observed on maize growth, but a decrease in the allocation of Cd to shoots between the 0.8 and 20 nM Cd exposures revealed that the plants already responded to these low concentrations of Cd according to a shoot Cd excluder strategy. The Cd, Cu and Zn concentrations in shoots decreased with time as the result of an early decrease in the root/shoot ratio and of a decrease in the coefficient of allocation to aboveground for Zn and Cd at 20 nM. As a consequence, shoots of young plants were richer in micronutrients Cu and Zn but also in toxic Cd. The rate of delivery of Cd, Cu and Zn from xylem sap was successfully used to predict the time course of concentrations of Cd, Cu and Zn in the shoot. However, it overestimated the actual concentrations of Cd in the shoot, presumably because the reallocation of this trace element from shoots back to roots was not taken into account.

Cd, Zn, Cu, As, Fe, Cr, Ni, Al, and Pb were analyzed in the edible and inedible parts of the muricid gastropod Hexaplex trunculus sampled along the Tunisian coast in 2004, 2007, and 2011. The concentration ranges (μg/g dry weight) in the whole soft tissue were 0.1–19.2 for Cd, 198.7–564.6 for Zn, 31.9–363.1 for Cu, 12.8–177.8 for As, 35.4–179.0 for Fe, 0.0–5.8 for Cr, 0.1–4.6 for Ni, 1.0–41.4 for Al, and 0.0–0.6 for Pb. The highest concentrations were recorded in Gabès for Cd, Menzel Jemil for Zn and Cu, Bizerte channel for As, Zarat for Cr and Pb, and Tunis North Lake for Fe, Al, and Ni. The European standards compiled by FAO for mollusks were exceeded in several localities. The temporal trends revealed a decreasing metal contamination in most sampling stations from 2004 to 2011. The calculated intake of metals (μg/week/kg body weight) through human consumption of the snail edible portion varied from 0.0 to 4.4 of Cd, 55.9 to 172.1 of Zn, 8.7 to 92.7 of Cu, 3.0 to 42.6 of As, 9.5 to 49.1 of Fe, 0.0 to 1.52 of Cr, 0.0 to 1.4 of Ni, and 0.3 to 11.4 of Al. Comparison of these metal intakes with those of the standard provisional tolerable weekly intake (PTWI) values stipulated by the WHO recommends precaution in terms of human consumption of this marine snail.