We investigated the in situ applicability of the electrokinetic process with a hexagonal electrode configuration in order to remediate arsenic (As)-, copper (Cu)-, and lead (Pb)-contaminated paddy rice field soil at a field scale (width 17 m, length 12.2 m, and depth 1.6 m). An iron electrode was used in order to prevent the severe acidification of the soil near the anode. We selected ethylenediaminetetraacetic acid (EDTA) as a pursing electrolyte to enhance the extraction of Cu and Pb. The system removed 44.4 % of the As, 40.3 % of the Cu, and 46.6 % of the Pb after 24 weeks of operation. Fractionation analysis showed that the As bound to amorphous ion (Fe) and aluminum (Al) oxyhydroxides was changed into a form of As specifically bound. In the case of Cu and Pb, the fraction bound to Fe–Mn oxyhydroxide primarily decreased. The EDTA formed negatively charged complexes with Cu and Pb, and those complexes were transported toward the anode. The energy consumption was very low compared to that on a small scale because there was less energy consumption due to Joule heating. These results show that the in situ electrokinetic process could be applied in order to remediate paddy rice fields contaminated with multiple metals.

The aim of this study was to physically demonstrate the associations between Ni, Pb and Zn and the different soil components. To achieve this, several soil samples were observed by field emission-scanning electron microscope (FE-SEM) equipped with an energy dispersive spectrometer (EDS) detector. The samples came from mine sites vegetated and/or amended with wastes (sewage sludges and paper mill residues). The concentrations of metals in the different soil fractions were quantified by a chemical sequential extraction in a previous study. The sorption capacity of the soils was evaluated with sorption experiments using the batch method. We corroborated the results obtained by the sequential extraction of metals as well as the sorption experiments with the observations from the FE-SEM with the EDS. We physically observed the associations between Ni, Pb and Zn and oxides, organic matter and clays. We also observed PbCaCO₃ crystals in one of the soils, presumably formed during the sorption experiment. As it is not possible to know with complete certainty how Pb was retained by calcium in this soil by only using chemical methods, the use of microscopic techniques is crucial to ascertain how metals are associated with the different soil fractions.

Because the detrimental effects of chromium (Cr) to higher plants have been poorly investigated, the present study was undertaken to verify the toxic attributes of hexavalent chromium [Cr(VI)] to plant mitotic microtubules (MTs), to determine any differential disruption of MTs during mitosis of taxonomically related species and to clarify the relationship between the visualized chromosomal aberrations and the Cr(VI)-induced MT disturbance. For this purpose, 5-day-old uniform seedlings of Vicia faba, Pisum sativum, Vigna sinensis and Vigna angularis, all belonging to the Fabaceae family, were exposed to 250 μM Cr(VI) supplied as potassium dichromate (K₂Cr₂O₇) for 24, 72 and 120 h and others in distilled water serving as controls. Root tip samples were processed for tubulin immunolabelling (for MT visualization) and DNA fluorescent staining (for chromosomal visualization). Microscopic preparations of cell squashes were then examined and photographed by confocal laser scanning microscopy (CLSM). Cr(VI) halted seedling growth turning roots brown and necrotic. Severe chromosomal abnormalities and differential disturbance of the corresponding MT arrays were found in all mitotic phases. In particular, in V. faba MTs were primarily depolymerized and replaced by atypical tubulin conformations, whereas in P. sativum, V. sinensis and V. angularis they became bundled in a time-dependent manner. In P. sativum, the effects were milder compared to those of the other species, but in all cases MT disturbance adversely affected the proper aggregation of chromosomes on the metaphase plate, their segregation at anaphase and organization of the new nuclei at telophase. Cr(VI) is very toxic to seedling growth. The particular effect depends on the exact stage the cell is found at the time of Cr(VI) entrance and is species-specific. Mitotic MT arrays are differentially deranged by Cr(VI) in the different species examined, even if they are taxonomically related, while their disturbance underlies chromosomal abnormalities. Results furthermore support the view that MTs may constitute a reliable, sensitive and universal subcellular marker for monitoring heavy metal toxicity.

Persistent organic pollutants (POPs) have been of environmental and health concern for more than half a century and have their own intergovernmental regulation through the Stockholm Convention, from 2001. One major concern is the nursing child’s exposure to POPs, a concern that has led to a very large number of scientific studies on POPs in mothers’ milk. The present review is a report on the assessment on worldwide spatial distributions of POPs and of their temporal trends. The data presented herein is a compilation based on scientific publications between 1995 and 2011. It is evident that the concentrations in mothers’ milk depend on the use of pesticides and industrial chemicals defined as POPs. Polychlorinated biphenyls (PCBs) and “dioxins” are higher in the more industrialized areas, Europe and Northern America, whereas pesticides are higher in Africa and Asia and polybrominated diphenyl ethers (PBDEs) are reported in higher concentrations in the USA. POPs are consequently distributed to women in all parts of the world and are thus delivered to the nursing child. The review points out several major problems in the reporting of data, which are crucial to enable high quality comparisons. Even though the data set is large, the comparability is hampered by differences in reporting. In conclusion, much more detailed instructions are needed for reporting POPs in mothers’ milk. Temporal trend data for POPs in mothers’ milk is scarce and is of interest when studying longer time series. The only two countries with long temporal trend studies are Japan and Sweden. In most cases, the trends show decreasing concentrations of POPs in mothers’ milk. However, hexabromocyclododecane is showing increasing temporal concentration trends in both Japan and Sweden.

In this work, bioavailability and ecotoxicity of arsenite (As(III)) and arsenate (As(V)) species were compared between solution culture and soil system. Firstly, the adsorption of As(III) and As(V) was compared using a number of non-allophanic and allophanic soils. Secondly, the bioavailability and ecotoxicity were examined using germination, phytoavailability, earthworm, and soil microbial activity tests. Both As-spiked soils and As-contaminated sheep dip soils were used to test bioavailability and ecotoxicity. The sheep dip soil which contained predominantly As(V) species was subject to flooding to reduce As(V) to As(III) and then used along with the control treatment soil to compare the bioavailability between As species. Adsorption of As(V) was much higher than that of As(III), and the difference in adsorption between these two species was more pronounced in the allophanic than non-allophanic soils. In the solution culture, there was no significant difference in bioavailability and ecotoxicity, as measured by germination and phytoavailability tests, between these two As species. Whereas in the As-spiked soils, the bioavailability and ecotoxicity were higher for As(III) than As(V), and the difference was more pronounced in the allophanic than non-allophanic soils. Bioavailability of As increased with the flooding of the sheep dip soils which may be attributed to the reduction of As(V) to As(III) species. The results in this study have demonstrated that while in solution, the bioavailability and ecotoxicity do not vary between As(III) and As(V), in soils, the latter species is less bioavailable than the former species because As(V) is more strongly retained than As(III). Since the bioavailability and ecotoxicity of As depend on the nature of As species present in the environment, risk-based remediation approach should aim at controlling the dynamics of As transformation.

The efficiency of heterogeneous photocatalysis using N–F–TiO₂ as photocatalyst to degrade a priority pollutant, pentachlorophenol (PCP), in the presence of oxalates (OA) was investigated in detail. Response surface methodology was used to optimize the effect of three variables (catalyst concentration, OA/PCP ratio, and pH) on the photocatalytic degradation of pentachlorophenol. A quadratic model was established as a functional relationship between three independent variables and the degradation efficiency of PCP. The results of model fitting and statistical analysis demonstrated that the pH played a key role in the degradation of PCP. Within the studied experimental ranges, the optimum conditions for maximum PCP degradation efficiency (97.5 %) were: catalyst concentration 600 mg L⁻¹, OA/PCP ratio 2, and pH 10. The contribution of HO·, O₂ ·⁻, and e⁻ produced during the photocatalytic treatment was investigated with the addition of scavengers. The photocatalytic degradation was essentially proceeded through an oxidative mechanism at both acid and alkaline pH values by HO. and O₂ ·⁻ radicals attack. It was found that O₂ ·⁻ were the major reactive species involved in PCP degradation in pH 4 and HO· in pH 10.

Because of high emissions of anthropogenic as well as natural particles over the Indo-Gangetic Plains (IGP), it is important to study the characteristics of fine (PM₂.₅) and inhalable particles (PM₁₀), including their morphology, physical and chemical characteristics, etc., in Delhi during winter 2013. The mean mass concentrations of fine (PM₂.₅) and inhalable (PM₁₀) (continuous) was 117.6 ± 79.1 and 191.0 ± 127.6 μg m⁻³, respectively, whereas the coarse mode (PM₁₀–₂.₅) particle PM mass was 73.38 ± 28.5 μg m⁻³. During the same period, offline gravimetric monitoring of PM₂.₅ was conducted for morphological analysis, and its concentration was ~37 % higher compared to the continuous measurement. Carbonaceous PM such as organic carbon (OC) and elemental carbon (EC) were analyzed on the collected filters, and their mean concentration was respectively 33.8 and 4.0 μg m⁻³ during the daytime, while at night it was 41.2 and 10.1 μg m⁻³, respectively. The average OC/EC ratio was 8.97 and 3.96 during the day and night, respectively, indicating the formation of secondary organic aerosols during daytime. Effective carbon ratio was studied to see the effect of aerosols on climate, and its mean value was 0.52 and 1.79 during night and day, indicating the dominance of absorbing and scattering types of aerosols respectively into the atmosphere over the study region. Elemental analysis of individual particles indicates that Si is the most abundant element (~37–90 %), followed by O (oxide) and Al. Circularity and aspect ratio was studied, which indicates that particles are not perfectly spherical and not elongated in any direction. Trajectory analysis indicated that in the months of February and March, air masses appear to be transported from the Middle Eastern part along with neighboring countries and over Thar Desert region, while in January it was from the northeast direction which resulted in high concentrations of fine particles.

Oxygen penetration is a key determinant of sediment nitrification rates. In this study, we analyzed the effect of oxygen penetration on the sediment nitrification rate based on sediment oxygen profiles. Six sediments were designed to produce different oxygen profiles by adding different amounts of silica gel to the collected river mud. The oxygen profiles in the sediment were detected using a voltammetric microelectrode. With increased mud content, the sediment oxygen penetration depth decreased from 8.3 to 2.6 mm, and the oxygen concentration in the overlying water and at the sediment-water interface also showed a decreasing trend. The measured nitrification rate displayed a quadratic pattern that changed with the increase in mud content. Based on the detected oxygen profiles, the nitrification rate at each depth was calculated and summed to obtain the bulk sediment nitrification rate. The bulk sediment nitrification rate showed a consistently changing pattern with the measured rate. Oxygen profiles used to calculate nitrification rates could be approximated by the penetration depth (δ). The resulting nitrification model based on δ could explain the limiting role of oxygen penetration in sediment nitrification.

Energetic characterization of biomass allows for assessing its energy potential for application in different conversion processes into energy. The objective of this study is to physicochemically characterize pineapple crown leaves (PC) for their application in energy conversion processes. PC was characterized according to ASTM E871-82, E1755-01, and E873-82 for determination of moisture, ash, and volatile matter, respectively; the fixed carbon was calculated by difference. Higher heating value was determined by ASTM E711-87 and ash chemical composition was determined by XRF. The thermogravimetric and FTIR analyses were performed to evaluate the thermal decomposition and identify the main functional groups of biomass. PC has potential for application in thermochemical processes, showing high volatile matter (89.5 %), bulk density (420.8 kg/m³), and higher heating value (18.9 MJ/kg). The results show its energy potential justifying application of this agricultural waste into energy conversion processes, implementing sustainability in the production, and reducing the environmental liabilities caused by its disposal.