In situ phytoremediation of heavy metal–contaminated soil and groundwater: a green inventive approach

Environmental Science and Pollution Research - The heavy metal contamination of soil and groundwater is a serious threat to environment worldwide. The survival of human being primarily relies upon...     

Bioremediation of heavy metal–polluted environments by non-living cells from rhizobial isolates

Environmental Science and Pollution Research - Rhizosphere bacteria, for example, rhizobia, can play several roles, and one of the most important, the protection of plant roots against toxic...     

Separation and remediation of environmental pollutants using metal–organic framework-based tailored materials

Environmental Science and Pollution Research - Metal–organic frameworks (MOFs) are a polymer hybrid family of compounds comprising metal ions that have been deliberately incorporated in...     

Experimental study on treatment of heavy metal–contaminated soil by manganese-oxidizing bacteria

Environmental Science and Pollution Research - There are many studies on the treatment of heavy metals by manganese-oxidizing bacteria and the reaction is good; the problem of compound pollution of...     

A typical case study from smelter–contaminated soil: new insights into the environmental availability of heavy metals using an integrated mineralogy characterization

Environmental Science and Pollution Research - Mineralogy was an important driver for the environmental release of heavy metals. Therefore, the present work was conducted by coupling mineral...     

Remediation of polycyclic aromatic hydrocarbon and metal-contaminated soil by successive methyl-β-cyclodextrin-enhanced soil washing–microbial augmentation: a laboratory evaluation

Polycyclic aromatic hydrocarbon (PAH) and metal-polluted sites caused by abandoned coking plants are receiving wide attention. To address the associated environmental concerns, innovative remediation technologies are urgently needed. This study was initiated to investigate the feasibility of a cleanup strategy that employed an initial phase, using methyl-β-cyclodextrin (MCD) solution to enhance ex situ soil washing for extracting PAHs and metals simultaneously, followed by the addition of PAH-degrading bacteria (Paracoccus sp. strain HPD-2) and supplemental nutrients to treat the residual soil-bound PAHs. Elevated temperature (50 °C) in combination with ultrasonication (35 kHz, 30 min) at 100 g MCD L^?1 was effective in extracting PAHs and metals to assist soil washing; 93 % of total PAHs, 72 % of Cd, 78 % of Ni, 93 % of Zn, 84 % of Cr, and 68 % of Pb were removed from soil after three successive washing cycles. Treating the residual soil-bound PAHs for 20 weeks led to maximum biodegradation rates of 34, 45, 36, and 32 % of the remaining total PAHs, 3-ring PAHs, 4-ring PAHs, and 5(+6)-ring PAHs after washing procedure, respectively. Based on BIOLOG Ecoplate assay, the combined treatment at least partially restored microbiological functions in the contaminated soil. The ex situ cleanup strategy through MCD-enhanced soil washing followed by microbial augmentation can be effective in remediating PAH and metal-contaminated soil.     

Distribution-based effects of disaggregated GDP and environmental quality—a case of quantile on quantile estimates

Environmental Science and Pollution Research - There is a strong association between environmental quality and economic activity. Empirical studies term this relationship as environmental Kuznets...     

Preparation of calcium oxalate—bromopyrogallol red inclusion sorbent and application to treatment of cationic dye and heavy metal wastewaters

Background, aim, and scope  Dye pollutants are a major class of environmental contaminants. Over 100,000 dyes have been synthesized worldwide and more than 700,000 tons are produced annually and over 5% are discharged into aquatic environments. The adsorption or sorption is one of the most efficient methods to remove dye and heavy metal pollutants from wastewater. However, most of the present sorbents often bear some disadvantages, e.g. low sorption capacity, difficult separation of spoil, complex reproduction, or secondary pollution. Development of novel sorbents that can overcome these limitations is desirable. Materials and methods  On the basis of the chemical coprecipitation of calcium oxalate (CaC₂O₄), bromopyrogallol red (BPR) was embedded during the growing of CaC₂O₄ particles. The ternary C₂O₄ ^2––BPR–Ca²⁺ sorbent was yielded by the centrifugation. Its composition was determined by spectrophotometry and AAS, and its structure and morphology were characterized by powder X-ray diffraction (XRD), laser particle-size analysis, and scanning electron microscopy (SEM). The adsorption of ethyl violet (EV) and heavy metals, e.g. Cu(II), Cd(II), Ni(II), Zn(II), and Pb(II) were carried out and their removal rate determined by spectrophotometry and ICP-OES. The adsorption performance of the sorbent was compared with powder activated carbon. The Langmuir isothermal model was applied to fit the embedment of BPR and adsorption of EV. Results  The saturation number of BPR binding to CaC₂O₄ reached 0.0105 mol/mol and the adsorption constant of the complex was 4.70 × 10⁵ M^–1. Over 80% of the sorbent particles are between 0.7 and 1.02 μm, formed by the aggregation of the global CaC₂O₄/BPR inclusion grains of 30–50 nm size. Such a material was found to adsorb cationic dyes selectively and sensitively. Ethyl violet (EV) was used to investigate the adsorption mechanism of the material. One BPR molecule may just bind with one EV molecule. The CaC₂O₄/BPR inclusion material adsorbed EV over two times more efficiently than the activated carbon. The adsorption of EV on the CaC₂O₄/BPR inclusion sorbent was complete in only 5 min and the sedimentation complete in 1 h. However, those of EV onto activated carbon took more than 1.5 and 5 h, respectively. The treatment of methylene blue and malachite green dye wastewaters indicated that only 0.4% of the sorbent adsorbed over 80% of color substances. Besides, the material can also adsorb heavy metals by complexation with BPR. Over 90% of Pb²⁺, and approximately 50% of Cd²⁺ and Cu²⁺, were removed in a high Zn²⁺-electroplating wastewater when 3% of the material was added. Eighty-six percent of Cu²⁺, and 60% of Ni²⁺ and Cd²⁺, were removed in a high Cd²⁺-electroplating wastewater. Discussion  The embedment of BPR into CaC₂O₄ particles responded to the Langmuir isothermal adsorption. As the affinity ligand of Ca²⁺, BPR with sulfonic groups may be adsorbed into the temporary electric double layer during the growing of CaC₂O₄ particles. Immediately, C₂O₄ ^2– captured the Ca²⁺ to form the CaC₂O₄ outer enclosed sphere. Thus, BPR may be released and embedded as a sandwich between CaC₂O₄ layers. The adsorption of EV on the sorbent obeyed the Langmuir isothermal equation and adsorption is mainly due to the ion-pair attraction between EV and BPR. Different from the inclusion sorbent, the activated carbon depended on the specific surface area to adsorb organic substances. Therefore, the adsorption capacity, equilibrium, and sedimentation time of the sorbent are much better than activated carbon. The interaction of heavy metals with the inclusion sorbent responded to their coordination. Conclusions  By characterizing the C₂O₄ ^2––BPR–Ca²⁺ inclusion material using various modern instruments, the ternary in situ embedment particle, [(CaC₂O₄)₉₅(BPR)] _n ^2n–, an electronegative, micron-sized adsorbent was synthesized. It is selective, rapid, and highly effective for adsorbing cationic dyes and heavy metals. Moreover, the adsorption is hardly subject to the impact of electrolytes. Recommendations and perspectives  The present work provides a simple and valuable method for preparing the highly effective adsorbent. If a concentrated BPR wastewater was reused as the inclusion reactant, the sorbent will be low cost. By selecting the inclusion ligand with a special structure, we may prepare some particular functional materials to recover the valuable substances from seriously polluted wastewaters. The recommended method will play a significant role in development of advanced adsorption materials. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Heavy metal pollution and risks in a highly polluted and populated Indian river–city pair using the systems approach

Environmental Science and Pollution Research - A sectorial approach for assessing heavy metal pollution in rivers neglects the inter-relationship between its environmental compartments and thus...     

Pharmacological implications of ipriflavone against environmental metal–induced neurodegeneration and dementia in rats

Environmental Science and Pollution Research - Long-term exposure to environmental neurotoxic metals is implicated in the induction of dementia and cognitive decline. The present study aims to...     

Bioremediation of chlorinated pesticide–contaminated soil using anaerobic sludges and surfactant addition

Methanogenic granular sludge and wastewater fermented sludge were used as inocula for batch tests of anaerobic bioremediation of chlorinated pesticide contaminated soil. Results obtained for both types of biomass were similar: 80 to over 90% of γ -hexachlorocyclohexane (γ-HCH), 1,1,1-trichloro-2,2-bis-(4-methoxyphenyl)ethane (methoxychlor) and 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane (DDT) removed in 4–6 weeks. Residual fractions of these pesticides persisted till the end of the 16-week experiment. DDT was degraded through 1,1-dichloro-2,2-bis-(4-chlorophenyl)ethane (DDD). Accumulation of this product corresponded stoichiometrically only to 34–53% of removed DDT, supposedly due to its further transformations, finally resulting in formation of detected 4,4′-dichlorobenzophenone (DBP). Addition of 0.5 mM Tween 80 nonionic surfactant resulted in about a twofold decrease of γ -HCH and methoxychlor residual concentrations, as well as considerably lower DDD accumulation (7–29%) and higher DBP production. However, 1.25 mM dose of this surfactant applied together with granular sludge brought DDD levels back to that observed for treatments with the sludge alone, also impairing DBP formation.     

Changes in heavy metal contents in an acidic forest soil affected by depletion of soil organic matter within the time span 1969–93

Measurements of heavy metal content (Pb, Cd, Zn) were made in the period 1969–93 in a forested ecosystem near Möhlin (north-western part of Switzerland). Some distinct changes were found in the soil, especially in the subsoil (30–35 cm). The main and most likely driving force of the induced changes in the subsoil can be traced back to the observed decomposition of organic matter which strongly influenced the behaviour of major and minor chemical constituents of the soil. These changes are presumably mostly due to incidents that occurred in the past caused by the nearby aluminium industry. Generally, the observed changes in soil chemistry increase with decreasing distance to the aluminium plant in the time span 1969–93. The influence, if any, of the vegetation type and the forest management on the changes in the subsoil could not be figured out. Changes in the Pb content primarily correlate with soil organic matter (with a significant decrease in the subsoil). Good correlations are also found with Fe and partially with Al and Mn. Cd correlates well with pH, (earth)alkali ions, and generally to a lower degree with Mn, Fe and Al, but almost no correlation was found with the organic matter of the soil. Zn holds an intermediate position: significant correlations with organic C, (earth)alkali ions, Fe, Al and Mn were found but pH correlated only very weakly. The main transportation mechanism of Pb in the subsoil is believed to be primarily in colloidal form. Colloid release mechanisms are hypothesised to be due to the humus disintegration and the consequent reaction chain. In contrast to Pb, the elements Cd and Zn have, presumably, been translocated to a great extent as aqueous species.     

Vegetational and mycorrhizal successions at a metal polluted site: Indications for the direction of phytostabilisation?

Plant communities on plots with different metal pollution levels were compared in a field study in order to select the most suitable plant species for the direction of secondary succession toward the targeted grassland vegetation. The vegetational succession showed a gradual increase in plant cover and the number of plant species on the less polluted locations. Two predominant grass species Calamagrostis varia and Sesleria caerulea were selected for phytostabilisation, but a severely reduced seed germination capacity obstructed their use in practice. The mycorrhizal succession showed a gradual replacement of non-mycorrhizal with mycorrhizal plant species. Similar levels of arbuscular mycorrhizal colonisation of a particular plant species may be developed within each growing season regardless of the levels of pollution, with the exception of vesicle/intraradical spore formation. The results suggest that lower overall mycorrhizal colonisation levels and increased vesicle/spore formation may be a part of a mycorrhizal strategy at the most polluted locations.     

Nematode community structure as bioindicator of soil heavy metal pollution along an urban–rural gradient in southern Shenyang, China

Effects of heavy metals caused by urbanisation on soil nematode communities were investigated along an urban–suburban–rural gradient in southern Shenyang, China. The numbers of total nematodes increased significantly along the urban–rural gradient. Similar trends were observed in the values of Structure Index (SI), with lower values found in urban site and higher in the rural site. Generic richness and SI were sensitive indicators for assessing the effect of heavy metals on soil nematode communities. The Canonical Correspondence Analysis (CCA) indicated that copper concentration and Cation Exchange Capacity (CEC) were most important environmental parameters that influenced nematode distribution.     

The combined application of γ-PGA-producing bacteria and biochar reduced the content of heavy metals and improved the quality of tomato (Solanum lycopersicum L.)

Environmental Science and Pollution Research - Plant growth-promoting bacteria and biochar have been widely used as immobilizers to remediate heavy metal contaminated soil. However, few studies...     

Steel slag quality control for road construction aggregates and its environmental impact: case study of Vietnamese steel industry—leaching of heavy metals from steel-making slag

Environmental Science and Pollution Research - Steel slag is an industrial by product of steel manufacturing processes and has been widely utilized within civil and construction materials for road...     

Airborne heavy metal pollution and its effects on foliar elemental composition of Empetrum hermaphroditum and Vaccinium myrtillus in Sør-Varanger, northern Norway

Uptake of Al, Cu, Fe, Mn, Ni, Ca, K, Mg, P, and S in Empetrum nigrum L. ssp. hermaphroditum Hagerup and Vaccinium myrtillus L. from Ni, Cu and SO2 contaminated sites in S?r-Varanger, northern Norway, were investigated. The primary objective was to study the effect of airborne heavy metal pollution on foliar element composition of these two dwarf shrubs. Ni distribution and availability in soils clearly indicate atmospheric deposition of Ni particulates in S?r-Varanger. Foliar Ni concentrations in E. hermaphroditum and V. myrtillus increased in relation to plant available Ni in corresponding soils. Leaves of E. hermaphroditum generally contained higher concentrations of Ni than leaves of V. myrtillus. Emissions influenced some features of leaf elemental composition of the two species in very different ways. In leaves of V. myrtillus, S increased in proportion to Ni and Cu, while levels of Mn decreased. In leaves of E. hermaphroditum, Fe increased in proportion to Ni and Cu, while levels of Ca decreased.     

Sorption–desorption and transport of trimethoprim and sulfonamide antibiotics in agricultural soil: effect of soil type,dissolved organic matter,and pH

Use of animal manure is a main source of veterinary pharmaceuticals (VPs) in soil and groundwater through a series of migration processes. The sorption–desorption and transport of four commonly used VPs including trimethoprim (TMP), sulfapyridine, sulfameter, and sulfadimethoxine were investigated in three soil layers taken from an agricultural field in Chongming Island China and two types of aqueous solution (0.01 M CaCl₂ solution and wastewater treatment plant effluent). Results from sorption–desorption experiments showed that the sorption behavior of selected VPs conformed to the Freundlich isotherm equation. TMP exhibited higher distribution coefficients (K _d?=?6.73–9.21) than other sulfonamides (K _d?=?0.03–0.47), indicating a much stronger adsorption capacity of TMP. The percentage of desorption for TMP in a range of 8–12 % is not so high to be considered significant. Low pH (<pK _a of tested VPs) and rich soil organic matter (e.g., 0–20 cm soil sample) had a positive impact on sorption of VPs. Slightly lower distribution coefficients were obtained for VPs in wastewater treatment plant (WWTP) effluent, which suggested that dissolved organic matter might affect their sorption behavior. Column studies indicated that the transport of VPs in the soil column was mainly influenced by sorption capacity. The weakly adsorbed sulfonamides had a high recovery rate (63.6–98.0 %) in the leachate, while the recovery rate of TMP was only 4.2–10.4 %. The sulfonamides and TMP exhibited stronger retaining capacity in 20–80 cm and 0–20 cm soil samples, respectively. The transport of VPs was slightly higher in the columns leached by WWTP effluent than by CaCl₂ solution (0.01 M) due to their sorption interactions.     

Heavy metal–induced stress in eukaryotic algae—mechanisms of heavy metal toxicity and tolerance with particular emphasis on oxidative stress in exposed cells and the role of antioxidant response

Environmental Science and Pollution Research - Heavy metals is a collective term describing metals and metalloids with a density higher than 5&nbsp;g/cm3. Some of them are essential...