Effects of a lead- and cadmium-resistant fungal strain on the absorption of heavy metals by Vetiveria zizanioides北大核心CSCD

A two-factor randomized complete block experiment was used to explore the remediation by a plant-microorganism combination on soils contaminated by lead (Pb) and cadmium (Cd). Factor A was the amount of fungi, for which four values were considered, namely, 0, 1, 3, and 5 g. Factor B was the level of contamination by lead and cadmium, for which six values were considered, namely, Cd0Pb0, Cd10Pb400, Cd20Pb600, Cd30Pb800, Cd50Pb1200, and Cd80Pb1800 (data in units of mg/ kg). The results showed that the resistant fungi promoted the growth of vetiver (Vetiveria zizanioides). At weights of 1, 3, and 5 g, the resistant fungi increased the biomass of vetiver by 41.9%, 74.9%, and 71.7% respectively. The resistant fungi stimulated the absorption of lead and cadmium by both the aerial and underground parts of vetiver. In the presence of 80 mg/kg of Cd2+ and 1 800 mg/kg of Pb2+, the contents of lead in the aerial parts of vetiver were increased by 120.6%, 265.4%, and 242.9%, while the lead content in the underground parts were increased by 110.3%, 278.2%, and 266.2%, after the addition of 1 g, 3 g, and 5 g of fungi, respectively. The content of cadmium in the aerial parts increased by 113.2%, 238.3%, and 217.3%, while the content of cadmium in the underground parts increased by 103.1%, 298.8%, and 274.4%, after the addition of 1 g, 3 g, and 5 g of fungi, respectively. The addition of fungi strengthened the effect of V. zizanioides to remediate soils contaminated by lead and cadmium, and the remediation after the addition of 3 g of fungi was better than that after treatment with 1 g and 5 g of fungi. The combination of resistant fungi and the heavy metal enrichment plant, vetiver, under different concentrations of lead and cadmium showed that the fungi had a significant effect on the remediation of soils contaminated by lead and cadmium. © 2018 Science Press. All rights reserved.     

Projecting the environmental profile of Singapore's landfill activities: Comparisons of present and future scenarios based on LCA

This article aims to generate the environmental profile of Singapore's Semakau landfill by comparing three different operational options associated with the life cycle stages of landfilling activities, against a 'business as usual' scenario. Before life cycle assessment or LCA is used to quantify the potential impacts from landfilling activities, an attempt to incorporate localized and empirical information into the amounts of ash and MSW sent to the landfill was made. A linear regression representation of the relationship between the mass of waste disposed and the mass of incineration ash generated was modeled from waste statistics between years 2004 and 2009. Next, the mass of individual MSW components was projected from 2010 to 2030. The LCA results highlighted that in a 'business as usual' scenario the normalized total impacts of global warming, acidification and human toxicity increased by about 2% annually from 2011 to 2030. By replacing the 8000-tonne barge with a 10000-tonne coastal bulk carrier or freighter (in scenario 2) a grand total reduction of 48% of both global warming potential and acidification can be realized by year 2030. Scenario 3 explored the importance of having a Waste Water Treatment Plant in place to reduce human toxicity levels - however, the overall long-term benefits were not as significant as scenario 2. It is shown in scenario 4 that the option of increased recycling championed over all other three scenarios in the long run, resulting in a total 58% reduction in year 2030 for the total normalized results. A separate comparison of scenarios 1-4 is also carried out for energy utilization and land use in terms of volume of waste occupied. Along with the predicted reductions in environmental burdens, an additional bonus is found in the expanded lifespan of Semakau landfill from year 2032 (base case) to year 2039. Model limitations and suggestions for improvements were also discussed.     

An ecological risk assessment model for a pulsed contaminant emission into a wetland channel flow

As a continuation of the modelling on ecological degradation and hydraulic dispersion of pollutant emission into an idealized two-dimensional free-surface wetland flow (Zeng, L., Chen, G.Q., 2009b. Ecological degradation and hydraulic dispersion of contaminant in wetland. Ecol. Model., doi:10.1016/j.ecolmodel.2009.10.024), an ecological risk assessment model for the typical case of a pulsed contaminant emission into a realistic three-dimensional wetland channel flow is presented in this paper for the fate of cross-sectional mean concentration under environmental dispersion. An environmental dispersion model for the mean concentration is devised as an extension of Taylor’s classical analysis on dispersion in fluid flows. The velocity distribution and the environmental dispersivity in the fully developed steady flow through the wetland is found and illustrated with limiting cases covering various known solutions for the porous media flow between parallel plates, flow in a shallow wetland, sweeping flow in a densely vegetated wetland, and single phase flow in a channel. Obtained by Aris’s method of moments, the environmental dispersivity is shown characterized with multi-scale asymptotic time variations with stem dominated stage, transitional stage, and width-depth-stem dominated stage. Based on the solution for the evolution of contaminant cloud in the wetland channel flow, critical length and duration of the contaminant cloud with concentration beyond given environmental standard level are concretely illustrated for typical pollutant constituents in wastewater emission. Under the same emission intensity and environmental standard, the duration of contaminant cloud in the wetland channel is revealed shorter than that in a free surface wetland, due to the lateral effect.     

Influence of support on catalytic behavior of nickel catalysts in the steam reforming of ethanol for hydrogen production

Al₂O₃, MgO, SiO₂ and ZnO-supported nickel catalysts were prepared and evaluated in the ethanol steam reforming for hydrogen production. It is shown that the catalytic behavior can be influenced depending on the experimental conditions employed and chemical composition of the catalyst.     

CLIMATE VARIABILITY AND FLOOD FREQUENCY ESTIMATION FOR THE UPPER MISSISSIPPI AND LOWER MISSOURI RIVERS1

ABSTRACT: This paper considers the distribution of flood flows in the Upper Mississippi, Lower Missouri, and Illinois Rivers and their relationship to climatic indices. Global climate patterns including El Niño/Southern Oscillation, the Pacific Decadal Oscillation, and the North Atlantic Oscillation explained very little of the variations in flow peaks. However, large and statistically significant upward trends were found in many gauge records along the Upper Mississippi and Missouri Rivers: at Hermann on the Missouri River above the confluence with the Mississippi (p = 2 percent), at Hannibal on the Mississippi River (p < 0.1 percent), at Meredosia on the Illinois River (p = 0.7 percent), and at St. Louis on the Mississippi below the confluence of all three rivers (p = 1 percent). This challenges the traditional assumption that flood series are independent and identically distributed random variables and suggests that flood risk changes over time.     

Effect of long-term application of biosolids for land reclamation on surface water chemistry

Biosolids are known to have a potential to restore degraded land, but the long-term impacts of this practice on the environment, including water quality, still need to be evaluated. The surface water chemistry (NO3-, NH4+, and total P, Cd, Cu, and Hg) was monitored for 31 yr from 1972 to 2002 in a 6000-ha watershed at Fulton County, Illinois, where the Metropolitan Water Reclamation District of Greater Chicago was restoring the productivity of strip-mined land using biosolids. The mean cumulative loading rates during the past 31 yr were 875 dry Mg ha(-1) for 1120-ha fields in the biosolids-amended watershed and 4.3 dry Mg ha(-1) for the 670-ha fields in the control watershed. Biosolids were injected into mine spoil fields as liquid fertilizer from 1972 to 1985, and incorporated as dewatered cake from 1980 to 1996 and air-dried solids from 1987 to 2002. The mean annual loadings of nutrients and trace elements from biosolids in 1 ha were 735 kg N, 530 kg P, 4.5 kg Cd, 30.7 kg Cu, and 0.11 kg Hg in the fields of the biosolids-amended watershed, and negligible in the fields of the control watershed. Sampling of surface water was conducted monthly in the 1970s, and three times per year in the 1980s and 1990s. The water samples were collected from 12 reservoirs and 2 creeks receiving drainage from the fields in the control watershed, and 8 reservoirs and 4 creeks associated with the fields in the biosolids-amended watershed for the analysis of NO3- -N (including NO2- N), NH4+-N, and total P, Cd, Cu, and Hg. Compared to the control (0.18 mg L(-1)), surface water NO3- -N in the biosolids-amended watershed (2.23 mg L(-1)) was consistently higher; however, it was still below the Illinois limit of 10 mg L(-1) for public and food-processing water supplies. Biosolids applications had a significant effect on mean concentrations of ammonium N (0.11 mg L(-1) for control and 0.24 mg L(-1) for biosolids) and total P (0.10 mg L(-1) for control and 0.16 mg L(-1) for biosolids) in surface water. Application of biosolids did not increase the concentrations of Cd and Hg in surface water. The elevation of Cu in surface water with biosolids application only occurred in some years of the first decade, when land-applied sludges contained high concentrations of trace metals, including Cu. In fact, following the promulgation of 40 CFR Part 503, the concentrations of all three metals fell below the method detection level (MDL) in surface water for nearly all samplings. Nitrate in the surface water tends to be higher in spring, and ammonium, total P, and total Hg in summer and fall. Mean nitrate, ammonium, and total phosphorus concentrations were found to be greater in creeks than reservoirs. The results indicate that application of biosolids for land reclamation at high loading rates from 1972 to 2002, with adequate runoff and soil erosion control, had only a minor impact on surface water quality.     

Broadband UV spectroscopy system used for monitoring of SO2 and NO emissions from thermal power plants

A gas monitoring system based on broadband absorption spectroscopic techniques in the ultraviolet region is described and tested. The system was employed in real-time continuous concentration measurements of sulfur dioxide (SO₂) and nitric oxide (NO) from a 220-ton h^?1 circulating fluidized bed (CFB) boiler in Shandong province, China. The emission coefficients (per kg of coal and per kWh of electricity) and the total emission of the two pollutant gases were evaluated. The measurement results showed that the emission concentrations of SO₂ and NO from the CFB boiler fluctuated in the range of 750–1300 mg m^?3 and 100–220 mg m^?3, respectively. Compared with the specified emission standards of air pollutants from thermal power plants in China, the values were generally higher for SO₂ and lower for NO. The relatively high emission concentrations of SO₂ were found to mainly depend on the sulfur content of the fuel and the poor desulfurization efficiency. This study indicates that the broadband UV spectroscopy system is suitable for industrial emission monitoring and pollution control.     

Modelling pollutants dispersion and plume rise from large hydrocarbon tank fires in neutrally stratified atmosphere

Petrochemical industries normally use storage tanks containing large amounts of flammable and hazardous substances. Therefore, the occurrence of a tank fire, such as the large industrial accident on 11th December 2005 at Buncefield Oil Storage Depots, is possible and usually leads to fire and explosions. Experience has shown that the continuous production of black smoke from these fires due to the toxic gases from the combustion process, presents a potential environmental and health problem that is difficult to assess. The goals of the present effort are to estimate the height of the smoke plume, the ground-level concentrations of the toxic pollutants (smoke, SO₂, CO, PAHs, VOCs) and to characterize risk zones by comparing the ground-level concentrations with existing safety limits. For the application of the numerical procedure developed, an external floating-roof tank has been selected with dimensions of 85 m diameter and 20 m height. Results are presented and discussed. It is concluded that for all scenarios considered, the ground-level concentrations of smoke, SO₂, CO, PAHs and VOCs do not exceed the safety limit of IDLH and there are no “death zones” due to the pollutant concentrations.     

Examining the temperature dependence of ethanol (E85) versus gasoline emissions on air pollution with a largely-explicit chemical mechanism

The increased use of ethanol in transportation fuels warrants an investigation of its consequences. An important component of such an investigation is the temperature dependence of ethanol and gasoline exhaust chemistry. We use the Master Chemical Mechanism (MCM, version 3.1, LEEDS University) with the SMVGEAR II chemical ordinary differential solver to provide the speed necessary to simulate complex chemistry to examine such effects. The MCM has over 13,500 organic reactions and 4600 species. SMVGEAR II is a sparse-matrix Gear solver that reduces the computation time significantly while maintaining any specified accuracy. Although we use a box model for this study, we determine and demonstrate in a separate study that the speed of the MCM with SMVGEAR II allows the MCM to be modeled in 3-dimensions. We also verified the accuracy of the model in comparison with smog chamber data. We then use the model with species-resolved tailpipe emissions data for E85 (15% gasoline, 85% ethanol fuel blend) and gasoline vehicles to compare the impact of each on nitrogen oxides, organic gases, and ozone as a function of ambient temperature and background concentrations, using Los Angeles in 2020 as a base case. We use two different emissions sets – one is a compilation of exhaust and evaporative data taken near 24 °C and the other from exhaust data taken at ?7 °C – to determine how atmospheric chemistry and emissions are affected by temperature. We include diurnal effects by examining two day scenarios. We find that, accounting for chemistry and dilution alone, the average ozone concentrations through the range of temperatures tested are higher with E85 than with gasoline by ～7 part per billion volume (ppbv) at higher temperatures (summer conditions) to ～39 ppbv at low temperatures and low sunlight (winter conditions) for an area with a high nitrogen oxide (NOx) to non-methane organic gas (NMOG) ratio. The results suggest that E85's effect on health through ozone formation becomes increasingly more significant relative to gasoline at colder temperatures due to the change in exhaust emission composition at lower temperatures. Acetaldehyde and formaldehyde concentrations are also much higher with E85 at cold temperatures, which is a concern because both are considered to be carcinogens. These could have implications for wintertime use of E85. Peroxy acetyl nitrate (PAN), another air pollutant of concern, increases with E85 by 0.3–8 ppbv. The sensitivity of the results to box size, initial background concentrations, background emissions, and water vapor were also examined.