Chemically Modified Crop Residues as a Low-Cost Technique for the Removal of Heavy Metal Ions from Wastewater

Batch adsorption experiments were carried out to evaluate the effect of type of crop residues and chemical pretreatment solutions on the removal efficiency of heavy metal ions at different concentrations of synthetic wastewater solutions. Rice straw, cotton stalks, and maize stalks were pretreated with different solutions (i.e., sulfuric acid, oxalic acid, sodium hydroxide, and distilled water as the control treatment) in order to increase their metal-binding capacity. Results indicated that cotton stalks were the best biosorbent material according to their efficiency in removal of heavy metal ions. Sodium hydroxide was the best chemical pretreatment method for stimulating the biosorption capacity of crop residues. Ions of Pb²⁺ had the highest biosorption ratio among all competitive ions, whereas Mn²⁺ ions had the lowest. The removal efficiency decreased as the concentration of heavy metal ions increased in aqueous solutions. Sorption equilibrium isotherms could be described by the Langmuir model in most cases, whereas an isotherm of S shape was observed in other cases, which did not follow the Langmuir isotherm model. In conclusion, cotton stalks pretreated with sodium hydroxide could be used as an efficient technique for wastewater remediation prior to irrigation due to its low-cost, little processing, and high biosorption capacity.     

A Potential Solution to Mitigate Phosphorus Release Following Clearfelling in Peatland Forest Catchments

Since the 1950s, large areas of upland peat have been afforested in northern European countries. Due to the poor phosphorus (P) adsorption capacity and low hydraulic permeability in blanket peat soil and increased labile P sources, harvesting these blanket peat forests can significantly increase P concentrations in the receiving aquatic systems. This paper briefly reviews the current management practices on the control of P releases from forestry in Ireland and the UK, and proposes a possible novel practice??grass seeding clearfelled areas immediately after harvesting, which should reduce P release from blanket peat forest harvesting. The study was conducted in the Burrishoole Catchment in the west of Ireland. A field trial was carried out to identify the successful native grass species that could grow quickly in the blanket peat forest. The two successful grass species??Holcus lanatus and Agrostis capillaris??were sown in three blanket peat forest study plots with areas of 100, 360, and 660 m² immediately after harvesting. Areas without grass seeding were used as controls. One year later, the P content in the aboveground vegetation biomass of the three study plots were 2.83, 0.65, and 3.07 kg P?ha^?1, respectively, which were significantly higher than the value of 0.02 kg P?ha^?1 in the control areas. The water extractable phosphorus in the three study plots were 8.44, 9.83, and 6.04 mg?(kg dry soil)^?1, respectively, which were lower than the value of 25.72 mg?(kg dry soil)^?1 in the control sites. The results indicate that grass seeding of the peatland immediately after harvesting can quickly immobilize significant amounts of P and warrants additional research as a new Best Management Practice following harvesting in the blanket peatland forest to mitigate P release.     

Responses of Biochemical Markers in the Fish Prochilodus lineatus Exposed to a Commercial Formulation of Endosulfan

Among the most extensively used compounds for the pest control in Argentinean crops is the organochlorine endosulfan. The sublethal effects of the commercial endosulfan formulation on hematology and lipid peroxidation (LPO) of the neotropical fish Prochilodus lineatus were investigated. Firstly, we calculated acute toxicity (LC₅₀) in order to define sublethal concentrations (0, 1.2, and 2.4 ??g L^?1). Hematological and oxidative stress responses were assessed at 24, 48, and 96 h. Endosulfan exposure significantly diminished the hemoglobin concentration, mean cell hemoglobin, and total plasma protein and increased white blood cells count and plasma glucose after 96 h. Exposed fish showed an alteration of the differential leukocytes count, evidenced by more thrombocytes and monocytes and less lymphocytes and neutrophils. Endosulfan increased LPO levels in intestine, liver, and brain in both sublethal concentrations. The present results suggest that endosulfan produces biochemical and physiological alterations, including immunological disorders, and it is a good inductor of oxidative stress in P. lineatus.     

Enhanced Tolerance to Mercury in a Streptomycin-Resistant Strain of Euglena gracilis

Toxicity of Hg²⁺ was determined in two strains of Euglena gracilis var. bacillaris: the wild-type (B) and a streptomycin-resistant strain (Sm^r). Cells were cultured under 12-h dark/12-h light regime or under continuous darkness. In the dark/light cultures, cellular growth was severely diminished in the B strain by Hg²⁺, whereas only a slight decrease was attained in the Sm^r strain; Hg²⁺ also affected the photosynthetic and respiratory activities of the B strain, but not those of Sm^r strain. Under continuous darkness, cellular growth of both strains was lower than under dark/light cycles, but it was inhibited by Hg²⁺ to a much lesser extent. Cell culture by 5 days under continuous dark or by 8 days of dark/light cycles resulted in a higher intracellular content of mercury in B strain than in Sm^r strain. In contrast, in both culture conditions, the fraction of mercury removed from medium by B strain was lower than that attained by Sm^r strain, whereas the ability to bio-transform (reduce) Hg²⁺ was two times higher in the mutant strain. The results suggested that Sm^r strain cells acquired an ability to remove Hg²⁺ from the medium, which was not associated to accumulation and which conferred protection against mercury.     

Bioremediation of Mangroves Impacted by Petroleum

The majority of oil from oceanic oil spills (e.g. the recent accident in the Gulf of Mexico) converges on coastal ecosystems such as mangroves. Microorganisms are directly involved in biogeochemical cycles as key drivers of the degradation of many carbon sources, including petroleum hydrocarbons. When properly understood and managed, microorganisms provide a wide range of ecosystem services, such as bioremediation, and are a promising alternative for the recovery of impacted environments. Previous studies have been conducted with emphasis on developing and selecting strategies for bioremediation of mangroves, mostly in vitro, with few field applications described in the literature. Many factors can affect the success of bioremediation of oil in mangroves, including the presence and activity of the oil-degrading microorganisms in the sediment, availability and concentration of oil and nutrients, salinity, temperature and oil toxicity. More studies are needed to provide efficient bioremediation strategies to be applicable in large areas of mangroves impacted with oil. A major challenge to mangrove bioremediation is defining pollution levels and measuring recuperation of a mangrove. Typically, chemical parameters of pollution levels, such as polycyclic aromatic hydrocarbons (PAHs), are used but are extremely variable in field measurements. Therefore, meaningful mangrove monitoring strategies must be developed. This review will present the state of the art of bioremediation in oil-contaminated mangroves, new data about the use of different mangrove microcosms with and without tide simulation, the main factors that influence the success of bioremediation in mangroves and new prospects for the use of molecular tools to monitor the bioremediation process. We believe that in some environments, such as mangroves, bioremediation may be the most appropriate approach for cleanup. Because of the peculiarities and heterogeneity of these environments, which hinder the use of other physical and chemical analyses, we suggest that measuring plant recuperation should be considered with reduction in polycyclic aromatic hydrocarbons (PAHs). This is a crucial discussion because these key marine environments are threatened with worldwide disappearance. We highlight the need for and suggest new ways to conserve, protect and restore these environments.     

Heavy Metal Concentration Survey in Soils and Plants of the Les Malines Mining District (Southern France): Implications for Soil Restoration

Mining activities generate spoils and effluents with extremely high metal concentrations of heavy metals that might have adverse effects on ecosystems and human health. Therefore, information on soil and plant metal concentrations is needed to assess the severity of the pollution and develop a strategy for soil reclamation such as phytoremediation. Here, we studied soils and vegetation in three heavily contaminated sites with potential toxic metals and metalloids (Zn, Pb, Cd, As, TI) in the mining district of Les Malines in the Languedoc region (southern France). Extremely high concentrations were found at different places such as the Les Aviniéres tailing basins (up to 160,000 mg kg^?C1 Zn, 90,000 mg kg^?C1 Pb, 9,700 mg kg^?C1 of As and 245 mg kg^?C1 of Tl) near a former furnace. Metal contamination extended several kilometres away from the mine sites probably because of the transport of toxic mining residues by wind and water. Spontaneous vegetation growing on the three mine sites was highly diversified and included 116 plant species. The vegetation cover consisted of species also found in non-contaminated soils, some of which have been shown to be metal-tolerant ecotypes (Festuca arvernensis, Koeleria vallesiana and Armeria arenaria) and several Zn, Cd and Tl hyperaccumulators such as Anthyllis vulneraria, Thlaspi caerulescens, Iberis intermedia and Silene latifolia. This latter species was highlighted as a new thallium hyperaccumulator, accumulating nearly 1,500 mg kg^?C1. These species represent a patrimonial interest for their potential use for the phytoremediation of toxic metal-polluted areas.     

Geochemistry of Mercury Along a Soil Profile Compared to Other Elements and to the Parental Rock: Evidence of External Input

The vertical distribution of mercury along a weathering profile derived from a diabase was compared to the main geochemical and mineralogical characteristics of the soil and its parental rock. The sampling site was in a metropolitan area, nearby to an active quarry and relatively close to an industrial park. The samples of a 6-m-deep fresh exposure of the soil profile and also of fresh rock were collected during the dry season. Kaolinite, goethite, hematite, and residual primary minerals were identified in the soil samples. Typically, the concentrations of Hg in the soil are low. Whole samples contained between 1 (rock) and 37 ??g kg^?1 Hg, while the?<?63-??m soil fraction had up to 52 ??g kg^?1 Hg. The higher values of Hg corresponded to the upper layers of A (0?C10 cm) and B (200?C220 cm) soil horizons. Elemental gains and losses calculated against Zr resulted in the following order: Hg>>Pb?>?Zr?>?LREE?>?Nb?>?HREE?>?Al?>?Ti?>?Fe?>?Cr. Total organic carbon in soil samples varied between 0.2 and 5.1 g dm^?3, and correlation with Hg concentrations was moderate. The acid pH (4.2?C5.5) of the soil samples favors the sorption Hg species by predominant secondary phases like goethite and kaolinite. The Hg concentration of the rock is insufficient to explain the large enrichment of Hg along the soil profile, indicating that exogenic Hg, via atmospheric deposition, contributed to the measured Hg concentrations of the soil.     

Impact of Seasonal Fluctuations on the Sediment-Mercury, its Accumulation and Partitioning in Halimione portulacoides and Juncus maritimus Collected from Ria de Aveiro Coastal Lagoon (Portugal)

The availability of metals to plants is a complex function of numerous environmental factors. Many of these factors are interrelated, and vary seasonally and temporally. The current study intended to understand the influence of seasonal fluctuations and the vegetation of salt marsh plants (SMPs; Halimione portulacoides, Juncus maritimus) on sediment??s mercury (Hg) and its pH and redox potential (Eh), as well as their cumulative effect on the plant??s Hg-accumulation and Hg-partitioning potential. The area selected for the study was Laranjo Basin at Ria de Aveiro lagoon (Portugal) where a known Hg gradient was existed due to chlor-alkali plant discharge. Three sampling sites (L1, L2 and L3) were selected along a transect defined by the distance from the main Hg source. Samples were also collected from the Hg-free site (R). Irrespective of the plant vegetation, Hg in sediments gradually increased with a decreasing distance towards Hg-point source. The sediment colonised by J. maritimus showed more Hg concentration compared with H. portulacoides irrespective of the season. As a whole, J. maritimus accumulated Hg more than H. portulacoides at all the sampling sites, whereas in root, stem and leaf, the concentration was ranked as: L1 > L2 > L3 in both the plant species and was differentially influenced by seasonal changes. Moreover, root of both plants exhibited highest Hg concentration compared with stem and leaf. In addition, the leaf of H. portulacoides exhibited more Hg than leaves of J. maritimus. Bioaccumulation and translocation factors and dry weight were differentially influenced by seasonal changes. Taking together the results, the physico-chemical properties of sediment especially the sediment-Eh seems to be influnced by the type of plant vegetation and seasonal changes which in turn may have influenced the chemistry of sediments; thus, it enfluences the bioavalability of Hg and the Hg-retention capacity of both salt marsh sediments (SMSs) and SMPs (bioaccumulation factor). Moreover, SMSs vegetated by J. maritimus exhibited a stronger capacity for the retention and phytostabilization of Hg belowground (in sediments and/or roots) than those dominated by H. portulacoides. Conversely, those SMSs extensively vegetated by H. portulacoides are expected to translocate more Hg to aboveground parts, acting as a potential source of this metal to the marsh ecosystem. Therefore, J. maritimus and H. portulacoides may be used repectively for phytostabilization (in rhizosediments) and phytoextraction (by accumulation in aboveground plant tissue for subsequent plant removal).     

Tannin-Based Coagulants in the Depuration of Textile Wastewater Effluents: Elimination of Anthraquinonic Dyes

Two tannin-based coagulants have been tested on anthraquinonic dye elimination from aqueous solutions. Acquapol S5T, derived from Acacia mearnsii de Wild, and Silvafloc, derived from Schinopsis balansae, were found to be excellent agents in the destabilization of Alizarin Violet 3R dye and its elimination through coagulation from textile effluents. Both coagulants showed that high affinity to the dye molecule in a wide pH range and q values reaches significant levels (up to 0.5 mg mg^???1) with reasonable low coagulant doses. Dye?Ccoagulant system presented a consistent behavior if studied under the statistical perspective of a design of experiments, where initial dye concentration and coagulant dose were the operating variables. Finally, both coagulants seemed to follow a predictable theoretical model under the Langmuir hypothesis with an accurate adjusted r ² coefficient above 0.9.     

Studies in a Fixed-Bed Photocatalytic Reactor System Using Natural Materials for Degradation of a Dye Contaminant in Water

A fixed-bed photocatalytic reactor equipped with a cylindrical parabolic light concentrator was studied to remove organic dyes from water using natural volcanic ashes particles and nanostructured titania supported on volcanic ashes as photocatalytic materials. The influences of flow rate, photocatalyst and photocatalytic material adsorption capacity were studied. A fixed-bed photocatalytic reactor was designed and built in the laboratory; a methylene blue aqueous solution, used as model compound for dye contaminated water, was fed into the reactor. Methylene blue destruction efficiencies were monitored spectrophotometrically. Combined effects of dye adsorption and photodecomposition on photocatalyst were studied and compared by infrared spectroscopy.