PURPOSE: When fossil fuels on the Earth are used up, which kind of green energy can be used to replace them? Do every bioenergy generation or crop food chain results in environmental pollution? These questions are major concerns in a world facing restricted supplies of energy and food as well as environmental pollutions. To alleviate these issues, option biogases are explored in this paper. MATERIALS AND METHODS: Two types of biogas generators were used for modifying the traditional crop food chain [viz. from atmospheric CO2 photosynthesis to crops, crop stem/husk biowastes (burnt in cropland or as home fuels), to livestock droppings (dumping away), pork and people foods, then to CO2], via turning the biowaste pollutants into green bioenergies. By analyzing the traditional food chain via observation method, the drawbacks of by-product biowastes were revealed. Also, the whole cycle chain was further analyzed to assess its “greenness,” using experimental data and other information, such as the material balance (e.g., the absorbed CO2, investment versus generated food, energy, and wastes). RESULTS AND DISCUSSION: The data show that by using the two types of biogas generators, clean renewable bioenergy, crop food, and livestock meat could be continuously produced without creating any waste to the world. The modification chain largely reduced CO2 greenhouse gas and had a low-cost investment. The raw materials for the gas generators were only the wastes of crop stems and livestock droppings. Thus, the recommended CO2 bioenergy cycle chain via the modification also greatly solved the environmental biowaste pollutions in the world. CONCLUSIONS: The described two type biogases effectively addressed the issues on energy, food, and environmental pollution. The green renewable bioenergy from the food cycle chain may be one of suitable alternatives to fossil and tree fuels for agricultural countries.

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.

PURPOSE: The aim of this study is to investigate the potential effects of increased urbanization in the Athens city, Greece on the intrinsic features of the temporal fluctuations of the surface ozone concentration (SOC). METHODS: The detrended fluctuation analysis was applied to the mean monthly values of SOC derived from ground-based observations collected at the centre of Athens basin during 1901–1940 and 1987–2007. RESULTS: Despite the present-day SOC doubling in respect to SOC historic levels, its fluctuations exhibit long-range power-law persistence, with similar features in both time periods. This contributes to an improved understanding of our predictive powers and enables better environmental management and more efficient decision-making processes. CONCLUSIONS: The extensive photochemistry enhancement observed in the Athens basin from the beginning of the twentieth century until the beginning of the twenty-first century seems not to have affected the long memory of SOC correlations. The strength of this memory stems from its temporal evolution and provides the limits of the air pollution predictability at various time scales.

PURPOSE: The purpose of the research is to investigate the applicability of the low-cost natural biosorbents for the removal of Pb(II) ions from aqueous solution and effluent from battery industry. METHODS: Six different biosorbents namely rice straw, rice bran, rice husk, coconut shell, neem leaves, and hyacinth roots have been used for the removal of Pb(II) ions from aqueous solution in batch process. All the biosorbents were collected from local area near Kolkata, West Bengal, India. The removal efficiency was determined in batch experiments for each biosorbent. RESULTS: The biosorbents were characterized by SEM, FTIR, surface area, and point of zero charge. The sorption kinetic data was best described by pseudo-second-order model for all the biosorbents except rice husk which followed intraparticle diffusion model. Pb(II) ions adsorption process for rice straw, rice bran, and hyacinth roots were governed predominately by film diffusion, but in the case of rice husk, it was intraparticle diffusion. Film diffusion and intraparticle diffusion were equally responsible for the biosorption process onto coconut shell and neem leaves. The values of mass transfer coefficient indicated that the velocity of the adsorbate transport from the bulk to the solid phase was quite fast for all cases. Maximum monolayer sorption capacities onto the six natural sorbents studied were estimated from the Langmuir sorption model and compared with other natural sorbents used by other researchers. The Elovich model, the calculated values of effective diffusivity, and the sorption energy calculated by using the Dubinin–Radushkevich isotherm were indicated that the sorption process was chemical in nature. The thermodynamic studies indicated that the adsorption processes were endothermic. FTIR studies were carried out to understand the type of functional groups responsible for Pb(II) ions binding process. Regeneration of biosorbents were carried out by desorption studies using HNO3. Battery industry effluents were used for the application study to investigate applicability of the biosorbents. CONCLUSION: The biosorbents can be utilized as low-cost sorbents for the removal of Pb(II) ions from wastewater.

The prevalence of bisphenol A (BPA) in the environment has attracted increasing attention because of the toxicity of this manmade pollutant. However, the toxicity related to cardiac development remains largely unknown. In the present paper, we investigated the cardiac toxicity of BPA using marine medaka (Oryzias melastigma) embryos. At 2 days postfertilization (dpf), the embryos were continuously exposed to a low concentration of BPA (200 μg/L) for the whole embryonic stage. Heart rate and sinus venosus (SV)–bulbus arteriosus (BA) distance were measured under microscopy. The mRNA expression levels of genes were quantified by SYBR real-time RT-PCR, and hematoxylin and eosin (H&E) staining was used to examine the histology of fish larvae hearts. Neither the heart rate nor the SV-BA distance of the embryos was affected by BPA exposure. However, the mRNA expression levels of Na⁺–K⁺–ATPase, BMP4, COX-1, FGF8, GATA4, and NKX2.5 were all downregulated at the critical developmental stages (6 and 10 dpf). Interestingly, the mRNA expression levels of COX-2 and LERP were significantly upregulated at 10 dpf. The mRNA expressions of inflammation-related genes (TNFα, IL1β, SOD, and CCL11) were all significantly upregulated after exposure. Moreover, we found that both the body length and the body width decreased in the larvae after embryonic exposure to BPA. The distributed foci of inflammation were observed in the juveniles after 2 weeks’ depuration. Exposure to BPA at embryonic stages could alter the expression of heart development-related genes and inflammation-related genes of O. melastigma. The larvae hatched from exposed embryos showed the foci of inflammation in the heart ventricles and the decrease of the body length and width.

PURPOSE: This study presents a procedure to differentiate the local and remote sources of particulate-bound polycyclic aromatic hydrocarbons (PAHs). METHODS: Data were collected during an extended PM2.5 sampling campaign (2009–2010) carried out for 1 year in Venice-Mestre, Italy, at three stations with different emissive scenarios: urban, industrial, and semirural background. Diagnostic ratios and factor analysis were initially applied to point out the most probable sources. In a second step, the areal distribution of the identified sources was studied by applying the discriminant analysis on factor scores. Third, samples collected in days with similar atmospheric circulation patterns were grouped using a cluster analysis on wind data. Local contributions to PM2.5 and PAHs were then assessed by interpreting cluster results with chemical data. RESULTS: Results evidenced that significantly lower levels of PM2.5 and PAHs were found when faster winds changed air masses, whereas in presence of scarce ventilation, locally emitted pollutants were trapped and concentrations increased. This way, an estimation of pollutant loads due to local sources can be derived from data collected in days with similar wind patterns. Long-range contributions were detected by a cluster analysis on the air mass back-trajectories. Results revealed that PM2.5 concentrations were relatively high when air masses had passed over the Po Valley. However, external sources do not significantly contribute to the PAHs load. CONCLUSIONS: The proposed procedure can be applied to other environments with minor modifications, and the obtained information can be useful to design local and national air pollution control strategies.

The aim of this study was to establish the temporal trends and spatial distribution of Polycyclic Aromatic Hydrocarbons (PAHs) in Ria de Vigo by means of studying the PAH burden in wild mussels. The samples were collected in eight sites along the margins of the Ria de Vigo during November from 1998 to 2008 and Polycyclic Aromatic Hydrocarbon contents were determined using high performance liquid chromatography–fluorescence derivatization (HPLC–FLD). Quality of chemical analysis was guaranteed by participation in QUASIMEME intercalibration exercises carried out during the period of analysis. The concentrations for the sum of 13 PAHs were in the range 24–480 μg/kg dw, typical of an urban and industrialized area (50–500 μg/kg dw) except for a punctual input in La Guía in 1998 that led to a concentration above 1,000 μg/kg dw. In general, the sites in the outermost section of the estuary (ría) showed the lowest values, with an increasing gradient in the medium and inner parts of the ría. Temporal patterns show, in general, a downward trend. The relative proportion of 3 and 4 ring PAHs also varies with the site, the former being predominant in the outermost area and the latter in the medium and inner parts of the ría. This is consistently related with the sources and processes taking place in different areas of the estuary.

INTRODUCTION: Microcystins (MCs; cyclic heptapeptides) are produced by freshwater cyanobacteria and cause public health concern in potable water supplies. There are more than 60 types of MCs identified to date, of which MC-LR is the most common found worldwide. For MC-LR, the WHO has established a threshold value of 1 μg L−1 for drinking water. The present MCs removal methods such as coagulation, flocculation, adsorption, and filtration showed low efficiency for removing dissolved MC fraction from surface waters to the stipulated limit prescribed by WHO based on MC health impacts. The search for cost-effective and efficient removal method is still warranted for remediation of dissolved MC-LR-contaminated water resources. MATERIALS AND METHODS: Molecularly imprinted polymer (MIP) adsorbent has been prepared using non-covalent imprinting approach. Using MC-LR as a template, itaconic acid as a functional monomer, and ethylene glycol dimethacrylate as a cross-linking monomer, a MIP has been synthesized. Computer simulations were used to design effective binding sites for MC-LR binding in aqueous solutions. Batch binding adsorption assay was followed to determine binding capacity of MIP under the influence of environmental parameters such as total dissolved solids and pH. RESULTS AND DISCUSSION: The adsorptive removal of MC-LR from lake water has been investigated using MIPs. The MIP showed excellent adsorption potential toward MC-LR in aqueous solutions with a binding capacity of 3.64 μg mg−1 which is about 60% and 70% more than the commercially used powdered activated carbon (PAC) and resin XAD, respectively. Environmental parameters such as total organic carbon (represented as chemical oxygen demand (COD)) and total dissolved solids (TDS) showed no significant interference up to 300 mg L−1 for MC-LR removal from lake water samples. It was found that the binding sites on PAC and XAD have more affinity toward COD and TDS than the MC-LR. Further, the adsorption capacity of the MIP was evaluated rigorously by its repeated contact with fresh lake water, and it was found that the adsorption capacity of the MIP did not change even after seven adsorption/desorption cycles. The contaminated water of MC-LR (1.0 μg L−1) of 3,640 L could be treated by 1 g of MIP with an estimated cost of US $1.5. CONCLUSIONS: The adsorption capacity of the MIP is 40% more than commercially used PAC and resins and also the polymer showed reusable potential which is one of the important criteria in selection of cyanotoxins remediation methods.

Fusarium wilt of cucumber caused by the fungus, Fusarium oxysporum, is one of the most destructive soilborne diseases and can result in serious economic loss. No efficient fungicide is currently available to control the disease. The aim of this study was to examine the disease suppression ability of pig manure and sludge composts in peat-based container media and explore the possible disease suppression mechanisms. Pig manure and sewage sludge compost were made in laboratory-scale tanks. Plant growth media were formulated with peat mixture and compost (or 60 °C heated compost) in a 4:1 ratio (v/v). Cucumber seedlings were artificially inoculated with F. oxysporum conidia (5 × 105 conidia mL−1) by the root-dip method. Cucumber Fusarium wilt was effectively suppressed in sludge compost-amended media, while the disease suppression effect of pig manure compost was limited. The ammonia levels in the manure compost-amended media were significantly higher than those of sludge compost-amended media, which could explain its lower disease suppression ability. Heated composts behaved similarly with respect to disease suppression. Adding composts increased microbial biomass, microbial activity, and the microbial diversity of the growth media. PCR-DGGE results indicated that the fungal community had a significant correlation to the disease severity. The artificially inoculated pathogen was retrieved in all treatments and one possible biocontrol agent was identified as a strain of F. oxysporum by phylogenetic analyses. The results indicated that the sludge compost used in this study could be applied as a method for biocontrol of cucumber Fusarium wilt.

PURPOSE: This research is on the evaluation of biosorption capability of the core of Artocarpus odoratissimus (Tarap), grown in Brunei Darussalam, towards Cd(II) and Cu(II) ions present in synthetic solutions, and to characterize the surface of Tarap particles. METHODS: Thermogravimetric analysis and surface titrations were conducted to characterize the surface of dried Tarap core particles. Atomic absorption spectroscopic measurements were conducted to determine the extent of removal of Cd(II) and Cu(II) under different experimental conditions. RESULTS: Mass reductions associated with many exothermic reaction peaks were observed beyond 200°C up to 650°C indicating the combustion of organic matter in Tarap. Dried particles of core of Tarap bear a negative surface charge promoting strong interaction towards positively charged ions, such as Cu(II) and Cd(II). Biosorption of the two metal ions on Tarap, which is relatively high beyond pH = 4, occurs within a short period of exposure time. The extent of biosorption is enhanced by acid treatment of the biosorbent, and further it does not significantly depend on the presence of nonreacting ions up to an ionic strength of 2.0 M. CONCLUSION: Strong attraction between each metal ion and the biosorbent is attributed to the negative surface charge on the biosorbent within a broad pH range. Acid treatment of the biosorbent improves sorption characteristics, suggesting that ion exchange plays an important role in the metal ion—biosorbent interaction process.