Pertinence of nutriments for a stalwart body

Environmental Science and Pollution Research - Nutrition plays a significant role in the prevention and treatment of common diseases. Some superb dietary choices such as functional foods and...     

Lichens reveal air PAH fractionation in the Himalaya

This paper shows that gas/particulate phase partitioning of polycyclic aromatic hydrocarbons (PAHs) can be monitored using lichens. Anthropogenic sources are responsible for the release of PAHs, which are bioaccumulated in plants at various spatial scales based on their physicochemical properties. Atmospheric PAHs are distributed both in the gaseous and particulate states. Here, a lichen species, Dermatocarpon vellereum Zschacke, has been collected at different altitudes in and around the Rudraprayag valley, located in Central Himalayan region of India, in order to study the spatial distribution of PAHs in the valley. Results show that PAH concentration ranged from 0.136 to 4.96 μg g^?1. Findings reveal that the bioaccumulation of 2- and 3-ringed PAHs was higher in high-altitude samples, whereas bioaccumulation of fluoranthene, a 4-ringed PAH, showed higher concentration in samples from localities away from town centre. 5- and 6-ring PAHs were then confined to the lower altitude at the base of the valley, thus justifying their particulate-bound nature. This is the first report showing the utility of lichen to biomonitor PAHs in the Himalayan ecosystem.     

Lichens to distinguish urban from industrial PAHs

This paper shows that lichens can be used as biomonitors to distinguish urban from industrial polycyclic aromatic hydrocarbons (PAHs). PAHs are atmospheric pollutants originating mainly from incomplete combustion of fuels in vehicles and industry. The occurrence of PAHs in air is a serious health issue in urban areas and industrial areas because some PAHs are carcinogenic. Biomonitoring PAHs with lichens is generally applied for quantification of PAHs. However, the precise sources of PAHs are not well known. Here we use lichen to trace the source of PAHs. PAHs were analyzed in Pyxine subcinerea Stirton, a lichen species collected from twelve sites which vary from urban and industrial to periurban forest area of Haridwar, in the foothills of the Indian Himalayas. Total PAH concentration ranged between 1.25 and 187.3 μg g⁻¹. Results indicate a clear distinction between urban and industrial PAHs profile, using principal component analysis. Lichen sampled from industrial sites exhibited higher concentrations of two-, five-, and six-ringed PAHs, up to 60% of total PAHs, while samples from urban sites were dominated by four-ringed PAHs, predominantly fluoranthene and acenaphthylene. Molecular ratios indicate that combustion was the dominant source of origin of PAHs in industrial area, while urban sites showed mixed origin of PAHs, both pyro- and petrogenic.     

Economics and GHG emission reduction of a PLA bio-refinery system—Combining bottom-up analysis with price elasticity effects

This paper analyses energy savings, GHG emission reductions and costs of bio-refinery systems for polylactic acid (PLA) production. The systems comprise ‘multi-functional’ uses of biomass resources, i.e. use of agricultural residues for energy consumption, use of by-products, and recycling and waste-to-energy recovery of materials. We evaluate the performance of these systems per kg of bio-based polymer produced and per ha of biomass production. The evaluation is done using data of Poland assuming that biomass and PLA production is embedded in a European energy and material market. First, the performance of different bio-refinery systems is investigated by means of a bottom-up chain analysis. Second, an analysis is applied that derives market prices of products and land depending on the own-price elasticity of demand. Thus, the costs of bio-refinery systems depending on the demand of land and material are determined. It is found that all PLA bio-refinery systems considered lead to net savings of non-renewable energy consumption of 70–220 GJ/(ha yr) and net GHG emission reductions of 3–17 Mg CO_2eq/(ha yr). Most of these PLA bio-refinery systems lead to net costs for the overall system of up to 4600 €/(ha yr). PLA production from short rotation wood leads to net benefits of about 1100 €/(ha yr) if a high amount of a high value product, i.e. fibres, is produced. Multi-functionality is necessary to ensure the viability of PLA bio-refinery systems from biomass with regard to energy savings and GHG emission reduction. However, the multi-functional use of biomass does not contribute much to overall incomes. Multifunctional biomass use – especially the use of biomass residues for energy consumption – contributes significantly to savings of non-renewable energy sources. Own-price elasticity of the demand for materials influences the overall costs of the bio-refinery system strongly. The own-price elasticity of land demand markets could become important if bio-refineries are introduced on a large scale.     

Distribution Of Cadmium And Nickel Among Various Forms In Natural And Contaminated Soils Amended With Edta

Because of its strong chelating capacity, application of ethylenediaminetetraacetic acid (EDTA) to soils may change the amount and distribution of heavy metals among their various chemical forms. Therefore, a greenhouse experiment was conducted using two cultivars of Brassica species (Brassica juncea and Brassica carinata) as hyper accumulator test crops on natural and artificially Cd and Ni contaminated soils. Both natural and metal amended soils were treated with disodium salt of EDTA at 0 and 1 g kg^–1 soil. After harvest of crops, soil samples were fractionated into water soluble plus exchangeable (WE), carbonate (CARB), organic matter (OM), Mn oxide (MnOX), amorphous Fe oxide (AFeOX), crystalline Fe oxide (CFeOX) and residual (RES) fractions. In metal amended soils, Cd and Ni were found predominantly in the AFeOX fraction in the absence of EDTA application and in the WE fraction in EDTA treated soil. Application of EDTA resulted in the redistribution of Cd among different forms and increased significantly Cd in the WE fraction with a concomitant significant decrease in the OM fraction. In natural soils, more than 40% of the total Cd was present in the RES fraction while in contaminated soil it was only 5%. Nickel in the WE fraction increased significantly while it considerably decreased in the CARB, OM, MnOX, AFeOX and CFeOX fractions with EDTA addition. This indicated that applied EDTA is capable to move Cd and Ni from the less soluble or more stable forms (CARB, OM, MnOX, AFeOX and CFeOX) to the most soluble form (WE). N natural soils, Ni in the RES fraction was found upto 49%, whereas only 10% of the total Ni was observed in contaminated soil, irrespective of EDTA treatment. In general, the amount of Cd recovered after harvest of both the Brassica cultivars did not differ significantly in any fraction except the WE fraction. The amount of Ni recovered in the AFeOX fraction was significantly higher after harvest of B. juncea as compared to B. carinata.Readers should send their comments on this paper to: BhaskarNath@aol.com within 3 months of publication of this issue.     

Freeze–dried synthesized bifunctional biopolymer nanocomposite for efficient fluoride removal and antibacterial activity

Local fluoride contamination and bacterial infections in potable water have dangerous effects on the human body and are today a global concern. In this study, we have synthesized a pH-responsive bifunctional biopolymer nanocomposite (HAZ) of humic acid with incorporating aluminum zirconium bimetallic oxide by deep freeze–drying method. Fast nucleation and interconnection of nanoparticles form a highly porous network because of sublimation of frozen HAZ. This duo nanocomposite has efficiently worked for fluoride removal and showed potent antibacterial activity against the Escherichia coli Gram-negative and Staphylococcus aureus Gram-positive bacteria. The X-ray photoelectron spectroscopy (XPS) analysis demonstrates that the hydroxyl groups act as a pivot in the ion exchange process of adsorption, each element of bimetallic oxide primarily takes part in the adsorption mechanism. The maximum adsorption capacity of the adsorbent was 180.62 mg/g at pH seven. Thermodynamic parameters like Gibbs free energy change (ΔG⁰), entropy (ΔS⁰), and enthalpy (ΔH⁰) indicate that the process was endothermic, feasible, and taken place by a chemisorption mechanism. This is the first novel freeze–dried bifunctional biopolymer nanocomposite composed of humic acid natural polymer incorporated with Al–Zr metal oxide, and it exhibited three times higher adsorption efficacy with excellent antibacterial action at a concentration of 5 µg/mL of the nanocomposite.     

The chemical form of cobalt-60 in the marine sponge Spirastrella cuspidifera

The marine sponge Spirastrella cuspidifera Lamarck shows a remarkable capacity to concentrate cobalt-60 from its environment, the specific activity of the radionuclide being two orders of magnitude higher than that in the ambient water. This suggests a very slow equilibrium with stable cobalt. The chemical form of the deposited cobalt-60 has been investigated in S. cuspidifera collected from coastal waters in the vicinity of a nuclear power station. The majority of the cobalt-60, 75 to 85%, is readily extractable into distilled water. Chromatographic analysis of this soluble fraction shows that about 85% of the cobalt is present as a small-molecular weight complex of low stability. No binding to any specific protein could be identified. The possible mechanism for the preferential uptake of cobalt-60 by this species of sponge is discussed.     

Preliminary Report on Radon Concentration in Drinking Water and Indoor Air in Kenya

A screening survey has been carried out to determine activity concentrations of radon (²²²Rn) in drinking water and indoor air in various locations in Kenya. The concentration of ²²²Rn in water was measured using a liquid scintillation counter (LSC). Three different passive integrating devices were used in the measurements of ²²²Rn in air. In the short-term measurements, radon is absorbed in activated charcoal and the analyses were carried out using either LSC or gamma ray spectrometry. The long-term measurements were carried out using solid-state nuclear track detectors (SSNTD). The mean and maximum values of ²²²Rn concentrations in water are 37 and 410 Bq L^–1 and 100 and 1160 Bq m^–3, respectively, in air. The highest values were obtained from groundwater sources and in the basements of buildings. When these values are compared with the internationally recommended reference levels, there are indications of existence of radon problems in some of the water sources and the dwellings tested in this survey.