INTRODUCTION: The changes in photosynthetic pigments, chlorophyll fluorescence, protein content, and antioxidant enzymes were investigated in a foliose lichen Pyxine cocoes, which was subjected to increasing concentrations of arsenate. METHODS: The arsenate concentrations of 10, 25, 50, 75, 100, and 200 μM were sprayed every alternate day on the lichen thallus. The thalli were then harvested on 10, 20, 30, and 45 days. RESULTS: The quantity of photosynthetic pigments exhibited a decreasing trend till 20 days but increased from 30 days onwards. Concomitantly, chlorophyll fluorescence also showed a decreasing trend with increasing arsenic treatment duration as well as concentration. The higher concentration of arsenate was found to be deleterious to the photosynthesis of lichen as the chlorophyll fluorescence and the amount of pigments decreased significantly. The protein content of lichen increased uninterruptedly as the concentration of arsenate as well as duration of treatment increased. The activities of superoxide dismutase and ascorbate peroxide increased initially at lower concentration of arsenate but declined at higher concentrations and longer duration of treatment. CONCLUSIONS: The catalase activity was found to be most susceptible to arsenate stress as its activity started declining from very beginning of the experiment. P. cocoes also proved to be an excellent accumulator of arsenate whose concentration increased in the thallus corresponding to its increase in the treatment and duration. Thus, it can be utilized for active biomonitoring of arsenic pollution.

BACKGROUND, AIMS AND SCOPE: Current studies have paid little attention to the dynamism in urban spatial expansion and its possible environmental and health effects or to the health effects of rapid urban environmental change at different points along the urbanisation gradient. This study adopts a public health ecology approach to systematically understand the relationship between urbanisation, urban environmental change and human health in China. METHOD: Remote sensing image analysis, based on night light data at five different time periods in recent decades, was used to determine changes to the overall urban area. Through a review of the evidence on the relationships between environmental health, urbanisation and health, we advance a pathway framework for explaining urban human health ecology. The Spearman rank correlation coefficient was used to measure the correlation between disease prevalence and urbanisation level, adding a further dimension to a systemic understanding of urban health. RESULTS AND CONCLUSIONS: Urban areas have been increasing spatially, but unevenly, in recent decades, with medium and small cities also expanding rapidly in the past decade. Urbanisation and urban expansion result in changes to land use/coverage change, the urban environment and the residents’ lifestyle, which result in human health problems. Regions with the highest urbanisation level were more inclined to have a high prevalence of chronic disease in recent decades. An ecological public health approach provides insights into the multiple types of data which need to be routinely collected if human disease is not to become a barrier to social and economic development.

PURPOSE: The objectives of this research are to identify the functional groups and determine corresponding pK a values of the acidic sites on dried brown algae Cystoseira barbata using FTIR and potentiometric titrations, and to investigate the biosorption ability of biomass towards divalent nickel, cadmium, and lead ions. Adsorption was studied as a function of solution pH and contact time, and experimental data were evaluated by the Langmuir isotherm model. METHODS: CaCl2 pretreatment was applied to the sorbent for enhancing the metal uptake capacity. The effect of solution pH on biosorption equilibrium was investigated in the pH range of 1.5–5.0. Individual as well as competitive adsorption capacity of the sorbent were studied for metal cations and mixtures. RESULTS: The retention of the tested metal ions was mostly influenced from pH in the range of 1.5–2.5, then stayed almost constant up to 5.0, while Ni(II) uptake showed the highest variation with pH. Potentiometric titrations were performed to find the number of strong and weak acidic groups and their acidity constants. The density of strong and weak acidic functional groups in the biomass were found to be 0.9 and 2.26 mmol/g, respectively. The FTIR spectra of the sorbent samples indicated various functionalities on the biomass surface including carboxyl, hydroxyl, and amino and sulphonate groups which are responsible for the binding of metal ions. CONCLUSIONS: The capacity of the biomass for single metal ions (around 1 mmol/g) was increased to 1.3 mmol/g in competitive adsorption, Pb(II) showing the highest Langmuir intensity constant. Considering its extremely high abundance and low cost, C. barbata may be potentially important in metal ion removal from contaminated water and industrial effluents.

INTRODUCTION: This study focused on the assessment of the geochemistry and hydrology of the Imgok Creek–Young Dong tributary for the design of a field coal mine drainage treatment system. METHODS AND RESULTS: Examination of this site showed that the pH was greatly lowered by the addition of the Young Dong water, except in the month of March. The alkalinity was also affected; the concentrations of iron, aluminum, and sulfate were elevated at sites below the confluence; of these, iron was particularly problematic. High iron concentrations were primarily restricted to the acid rock drainage (ARD) (YD-9) water sources, whereas high aluminum concentrations were seen in both the ARD and in some of the upstream water sources. The acidity was primarily due to ferrous and ferric iron with a lesser amount of aluminum acidity. Except for the sampling in March, the flow was dominated by the ARD. This hydrologic condition resulted from the loads of iron, aluminum, sulfate, and acidity, among other constituents, that were dominated by the ARD. CONCLUSION: Finally, treatment activities should primarily focus on the ARD and specifically seek to remove ferrous and ferric iron from the treatment system.

INTRODUCTION: The kinetics of the transformation of ammonia and acid gases into components of PM2.5 has been examined. The interactions of existing aerosols and meteorology with the transformation mechanism have also been investigated. The specific objective was to discern the kinetics for the gas-to-particle conversion processes where the reactions of NH3 with H2SO4, HNO3, and HCl take place to form (NH4)2SO4, NH4NO3, and NH4Cl, respectively, in PM2.5. MATERIALS AND METHODS: A Teflon-based outdoor environmental chamber facility (volume of 12.5 m3) with state-of-the-art instrumentation to monitor the concentration–time profiles of precursor gases, ozone, and aerosol and meteorological parameters was built to simulate photochemical reactions. RESULTS AND DISCUSSION: The reaction rate constants of NH3 with H2SO4, HNO3, and HCl (i.e., k S, k N, and k Cl) were estimated as (1) k S = 2.68 × 10−4 (±1.38 × 10−4) m3/μmol/s, (2) k N = 1.59 × 10−4 (±8.97 × 10−5) m3/μmol/s, and (3) k Cl = 5.16 × 10−5 (±3.50 × 10−5) m3/μmol/s. The rate constants k S and k N showed significant day–night variations, whereas k Cl did not show any significant variation. The D/N (i.e., daytime/nighttime values) ratio was 1.3 for k S and 0.33 for k N. The significant role of temperature, solar radiation, and O3 concentration in the formation of (NH4)2SO4 was recognized from the correlation analysis of k S with these factors. The negative correlations of temperature with k N and k Cl indicate that the reactions for the formation of NH4NO3 and NH4Cl seem to be reversible under higher temperature due to their semivolatile nature. It was observed that the rate constants (k S, k N, and k Cl) showed a positive correlation with the initial PM2.5 levels in the chamber, suggesting that the existing surface of the aerosol could play a significant role in the formation of (NH4)2SO4, NH4NO3, and NH4Cl. CONCLUSIONS: Therefore, this study recommends an intelligent control of primary aerosols and precursor gases (NO x , SO2, and NH3) for achieving reduction in PM2.5 levels.

BACKGROUND, AIM, AND SCOPE: Soils of basaltic origin cause difficulties in environmental magnetic screening for heavy metal pollution due to their natural high background values. Magnetic parameters and heavy metal content of highly magnetic topsoils from the Deccan Trap basalts are investigated to assess their potential for use in environmental magnetic pollution screening. This work extends the fast and cost-effective magnetic pollution screening techniques into soils with high natural magnetic signals. MATERIALS AND METHODS: Fifty-five topsoil samples from N–S and W–E transects were collected and subdivided according to grain size using wet sieving technique. Magnetic susceptibility, soft isothermal remanent magnetization (Soft IRM), thermomagnetic analysis, scanning electron microscopy (SEM), and heavy metal analysis were performed on the samples. RESULTS: Magnetic analyses reveal a significant input of anthropogenic magnetic particulate matter within 6 km of the power plant and the adjacent ash pond. Results depend strongly on the stage of soil development and vary spatially. While results in the W, E, and S directions are easily interpretable, in the N direction, the contribution of the anthropogenic magnetic matter is difficult to assess due to high magnetic background values, less developed soils, and a more limited contribution from the fly ash sources. Prevailing winds towards directions with more enhanced values seem to have a certain effect on particulate matter accumulation in the topsoil. Thermomagnetic measurements show Verwey transition and Hopkinson peak, thus proving the presence of ferrimagnetic mineral phases close to the pollution source. A quantitative decrease of the anthropogenic ferrimagnetic mineral concentration with increased distance is evident in Soft IRM measurements. SEM investigations of quantitatively extracted magnetic particles confirm the fly ash distribution pattern obtained from the magnetic and heavy metal analyses. Evaluation of magnetic and chemical data in concert with the Pollution Load IndiceS (PLIS) of Pb, Zn, and Cu reveals a good relationship between magnetic susceptibility and the metal content. CONCLUSIONS: Integrated approaches in data acquisition of magnetic and chemical parameters enable the application of magnetic screening methods in highly magnetic soils. Combined data evaluation allows identification of sampling sites that are affected by human activity, through the deviation of the magnetic and chemical data from the general trend. It is shown that integrative analysis of magnetic parameters and a limited metal concentration dataset can enhance the quality of the output of environmental magnetic pollution screening significantly.

INTRODUCTION: Initial geosmin degradation was closely related to water temperature and natural geosmin concentration of sampling environment. Here, for the first time, we evaluated the biodegradation of geosmin by microorganisms in biofilm from biological treatment unit of actual potable water treatment plant. MATERIALS AND METHODS: At an initial geosmin concentration of 2,500 ng/l, efficient geosmin removal was confirmed throughout the year. Furthermore, in the presence of mixed musty odor compounds (geosmin and MIB) as carbon source, geosmin degradation was enhanced compared to sole carbon source (geosmin alone). RESULTS AND DISCUSSION: PCR-DGGE analysis revealed a rich community structure within the biofilm during rapid geosmin removal period, April. PCA revealed that the significant change in bacterial communities occurred from day 1 to day 2. Two novel geosmin-degrading bacteria were isolated from the biofilm of the biological treatment unit of Kasumigaura Water Purification, Waterworks Department, Japan. They belong to Methylobacterium sp. and Oxalobacteraceae bacterium, respectively. CONCLUSIONS: These studies provide further insights into the unknown microbiological processes that occur during the biological removal of geosmin through water treatment and could facilitate the geosmin bioremediation in contaminated habitats.

INTRODUCTION: The copper bioaccumulation by the floating Lemna minor and by the completely submerged Ranunculus tricophyllus as a function of exposure time and copper concentration was studied, with the aim of proposing these species as environmental biosensors of the water pollution. RESULTS: The results show that both these aquatic angiosperms are good indicators of copper pollution because the copper uptake is the only function of metal concentration (water pollution). CONCLUSION: Uptake behavior is reported as a function of the time and concentration, based on the results of a 3-year study. Kinetic evaluations are proposed.

INTRODUCTION: Titanium dioxide (TiO2) nanoparticle powders have been extensively studied to quickly photodegrade some organic pollutants; however, the effect of the particle size of TiO2 nanoparticle aggregates on degradation remains unclear because microscale aggregates form once the nanoparticle powders enter into water. METHODS: The degradation of azo dye by different particle sizes of TiO2 nanoparticle aggregates controlled by NaCl concentrations was investigated to evaluate the particle size effect. Removal reactions of reactive black 5 (RB5) with TiO2 nanoparticles followed pseudo-first-order kinetics. RESULTS: The increase of TiO2 dosage from 40 to 70 mg/L enhanced the degradation. At doses around 100 mg/L TiO2, degradation rates decreased which could be the result of poor UV light transmittance at high-particle concentrations. At average particle sizes of TiO2 nanopowders less than around 500 nm, the degradation rates increased with decreasing particle size. As the average particle size exceeded 500 nm, the degradation rates were not significantly changed. CONCLUSIONS: For the complete degradation experiments, the mineralization rates of total organic carbon disappearance are generally following the RB5 decolorization kinetic trend. These findings can facilitate the application of TiO2 nanoparticles to the design of photodegradation treatments for wastewater.

INTRODUCTION: High concentrations of hexabromocyclododecane (HBCD) sometimes recorded in free-range hens' eggs are thought to be due to soil ingestion. Of the three stereoisomers of HBCD (α-, β-, and γ-HBCD), γ-HBCD is the main component in the commercial mixture, as well as in environmental matrices, whereas the isomer profile is α-dominated in biota. In fish and in mammals, this shift is thought to be due to a rapid elimination of γ-HBCD and to its bioisomerization to the more persistent α-HBCD. The aim of the current controlled study was to better understand the fate of ingested HBCD in laying hens. The isomer profile in soil being γ-dominated, excretion kinetics of γ-HBCD into egg yolk, and accumulation in liver and in abdominal fat were investigated. MATERIALS AND METHODS: Forty-eight laying hens were individually housed and fed with a spiked diet containing 1.1-ng γ-HBCD per gram for 21 days and with a clean diet for the following 18 days. Hens were sequentially slaughtered throughout the 39-day experiment. α-, β-, and γ-HBCD were analyzed in egg yolk, in abdominal fat, and in liver by LC-MS/MS. α- and γ-HBCD were quantified in the three tissues, while β-HBCD was never quantified. RESULTS AND CONCLUSION: Kinetics of the two isomers suggests that γ-HBCD is rapidly biotransformed and eliminated, and partly isomerized into the more persistent α-HBCD. Carry-over rate of ingested γ-HBCD to egg yolk was estimated at 1.2%. Estimated half-lives of γ-HBCD in egg yolk, in abdominal fat, and in liver were 2.9, 13, and 0.41 days, respectively.