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961.
Jörg Luster Manoj Menon Sandra Hermle Rainer Schulin Madeleine S. Günthardt-Goerg Bernd Nowack 《Water, Air, & Soil Pollution: Focus》2008,8(2):163-176
Soil translocation for recultivation of soil removed from construction sites and for the preparation of refilled lysimeters
inevitably involves disturbance of soil structure, and, if intermediate storage is included, also drying and rewetting of
the soil. We report on an experiment with model forest ecosystems, where uncontaminated forest subsoils were covered with
non-contaminated or freshly heavy metal (mainly Zn and Cu) contaminated topsoil in large lysimeters. Monitoring of the chemical
composition of the drainage water revealed two distinct soil conditioning phases. During an initial phase of about a year
strongly elevated nitrate and sulfate concentrations occurred that were attributed to a mineralisation flush caused by the
increased accessability of mineralisable nitrogen and sulfur in destroyed aggregates. These effects were significantly larger
in lysimeters with calcareous subsoil than in those with acidic subsoil. The second phase was characterised by a gradual decrease
in dissolved organic carbon and sulfate concentrations, in particular in the acidic subsoil. This decrease may be attributed
to the depletion of pools made accessible during aggregate destruction or the formation of new aggregates. These chemical
changes had only little effects on the concentrations of copper and zinc in the drainage water. Based on our results, it can
be concluded that large refilled lysimeters can be used for many purposes without risk of compromised results, if a conditioning
phase of about 1 year with sufficiently moist soil conditions is respected. Nevertheless, gradual changes in soil chemical
characteristics still occur after this initial phase. Implications for the recultivation of sites using relocated soils are
discussed. 相似文献
962.
963.
K. Pritsch D. Ernst F. Fleischmann S. Gayler T. E. E. Grams A. Göttlein W. Heller N. Koch H. Lang R. Matyssek J. C. Munch M. Olbrich H. Scherb S. Stich J. B. Winkler M. Schloter 《Water, Air, & Soil Pollution: Focus》2008,8(2):139-154
A lysimeter study was performed to monitor effects of elevated ozone on juvenile trees of Fagus sylvatica L. as well as on the plant–soil system. During a fumigation period over almost three growing seasons, parameters related
to plant growth, phenological development and physiology as well as soil functions were studied. The data analyses identified
elevated ozone to delay leaf phenology at early and to accelerate it at late developmental stages, to reduce growth, some
leaf nutrients (Ca, K) as well as some soluble phenolics (hydroxycinnamic acid derivatives, total flavonol glycosides). No
or very weak ozone effects were found in mobile carbon pools of leaves (starch, sucrose), and other phenolic compounds (flavans).
Altered gene expression related to stress and carbon cycling corresponded well with findings from leaf phenology and chemical
composition analyses indicating earlier senescence and oxidative stress in leaves under elevated ozone. Conversely in the
soil system, no effects of ozone were detected on soil enzyme activities, rates of litter degradation and lysimeter water
balances. Despite the fact that the three reported years 2003–2005 were climatically very contrasting including a hot and
dry as well as an extremely wet summer, and also mild as well as cold winters, the influence of ozone on a number of plant
parameters is remarkably consistent, further underlining the phytotoxic potential of elevated tropospheric ozone levels. 相似文献
964.
965.
Reiner Schroll Sabine Grundmann Ulrike Dörfler Bernhard Ruth Jean Charles Munch 《Water, Air, & Soil Pollution: Focus》2008,8(2):209-216
Several lysimeter scenarios and approaches exist to study the fate of agro-chemicals or contaminants from deposition in soil
columns. In many systems just transport and leaching of the parent compound is followed, in some systems the leaching and
transport of the metabolites is investigated as well. In more sophisticated lysimeter systems the volatilization and also
the mineralization of the applied chemicals can be additionally monitored. Depending on the lysimeter system used and on the
fact whether the applied chemicals are 14C-labeled or not, different results and various interpretations of the results might be achieved. Different lysimeter systems
are described in this paper and a real dataset of a specific lysimeter experiment was transferred and evaluated in a virtual
approach in the different lysimeter systems in order to show the advantages and disadvantages of the various systems. 相似文献
966.
Hang Seok Choi Seock Joon Kim Kwan Tae Kim 《Journal of Material Cycles and Waste Management》2008,10(1):1-6
The mixing characteristics of a passive scalar in the turbulent flow of a selective catalytic reduction process were numerically
and experimentally investigated, focusing especially on an injection nozzle with multiple holes for the reducing agent. The
multihole injection nozzle studied has six holes that are perpendicular to the ambient flue gas flow and are located near
the tip of the nozzle. Large eddy simulation was applied to the turbulent flow and mixing fields to elucidate the mixing mechanism
of the proposed nozzle compared with the single-hole nozzle that is commonly used in the conventional selective catalytic
reduction process. From the results, there exist broader regions of higher turbulent intensities for the multihole nozzle
than for the conventional single-hole nozzle. These regions are well matched with the positions of high vorticity in the near
upstream region of the jet flow issuing from the multiple holes of the nozzle. Consequently, the high turbulent intensities
and vorticity magnitudes lead to intensified mixing between the flue gas and the reducing agent. Hence, the most suitable
molar ratio between NOx and the reducing agent for the catalytic reaction can be easily obtained within a shorter physical
mixing length as a result of the enhanced scalar mixing. Finally, the numerical results were applied to a trial design version
of a multihole nozzle, and this nozzle was experimentally tested to confirm its mixing performance. 相似文献
967.
Leaching behavior of heavy metals from municipal solid waste incineration bottom ash and its geochemical modeling 总被引:1,自引:1,他引:0
Hua Zhang Pin-Jing He Li-Ming Shao Xin-Jie Li 《Journal of Material Cycles and Waste Management》2008,10(1):7-13
With the increase in the number of municipal solid waste incineration (MSWI) plants constructed in China recently, great attention
has been paid to the heavy metal leaching toxicity of MSWI residues. In this study, the effects of various parameters, including
extractant, leaching time, liquid-to-solid ratio, leachate pH, and heavy metal content, on the release properties of Cd, Cr,
Cu, Ni, Pb, and Zn from MSWI bottom ash were investigated. Partial least-squares analysis was employed to highlight the interrelationships
between the factors and response variables. Both experimental research and geochemical modeling using Visual MINTEQ software
were conducted to study the pH-dependent leaching behavior of these metals in fresh and weathered bottom ash, considering
precipitation/dissolution and surface complexation reactions (adsorption by hydrous ferric oxide and amorphous aluminum oxide/hydroxide).
The results showed that leachate pH was the predominant factor influencing heavy metal leachability. The leaching of Cu, Pb,
and Zn was mainly controlled by precipitation/dissolution reactions, whereas surface complexation had some effect on the leaching
of Cr, Cd, and Ni for certain pH ranges. The modeling results aggreed well with the experimental results.
Part of this work was presented at the Fourth International Conference on Combustion, Incineration/Pyrolysis and Emission
Control (i-CIPEC) 相似文献
968.
Increased salinity in spawning and nursery grounds in the Savannah River estuary was cited as the primary cause of a 97% decrease
in adult striped bass (Morone saxatilis) and a concomitant 96% decrease in striped bass egg production. Restoration efforts focused on environmental remediation
and stock enhancement have resulted in restored salinity patterns and increased egg and adult abundances. However, future
water needs or harbor development may preclude further recovery by reducing freshwater inflow or increasing salinity intrusion.
To assess the effect of potential changes in the salinity regime, we developed models relating discharge, tidal phase, and
salinity to striped bass egg and early larval survival and re-cast these in a quantitative Bayesian belief network. The model
indicated that a small upstream shift (≤1.67 km) in the salinity regime would have the least impact on striped bass early
life history survival, whereas shifts >1.67 km would have progressively larger impacts, with a 8.33-km shift potentially reducing
our estimated survival probability by >28%. Such an impact could have cumulative and long-term detrimental effects on the
recovery of the Savannah River striped bass population. The available salinity data were collected during average and low
flows, so our model represents some typical and some extreme conditions during a striped bass spawning season. Our model is
a relatively simplistic, “first-order” attempt at evaluating potential effects of changes in the Savannah River estuarine
salinity regime and points to areas of concern and potential future research. 相似文献
969.
A strategy for aromatic hydrocarbon bioremediation under anaerobic conditions and the impacts of ethanol: a microcosm study 总被引:7,自引:0,他引:7
Increased use of ethanol-blended gasoline (gasohol) and its potential release into the subsurface have spurred interest in studying the biodegradation of and interactions between ethanol and gasoline components such as benzene, toluene, ethylbenzene and xylene isomers (BTEX) in groundwater plumes. The preferred substrate status and the high biological oxygen demand (BOD) posed by ethanol and its biodegradation products suggests that anaerobic electron acceptors (EAs) will be required to support in situ bioremediation of BTEX. To develop a strategy for aromatic hydrocarbon bioremediation and to understand the impacts of ethanol on BTEX biodegradation under strictly anaerobic conditions, a microcosm experiment was conducted using pristine aquifer sand and groundwater obtained from Canadian Forces Base Borden, Canada. The initial electron accepter pool included nitrate, sulfate and/or ferric iron. The microcosms typically contained 400 g of sediment, 600 approximately 800 ml of groundwater, and with differing EAs added, and were run under anaerobic conditions. Ethanol was added to some at concentrations of 500 and 5000 mg/L. Trends for biodegradation of aromatic hydrocarbons for the Borden aquifer material were first developed in the absence of ethanol, The results showed that indigenous microorganisms could degrade all aromatic hydrocarbons (BTEX and trimethylbenzene isomers-TMB) under nitrate- and ferric iron-combined conditions, but not under sulfate-reducing conditions. Toluene, ethylbenzene and m/p-xylene were biodegraded under denitrifying conditions. However, the persistence of benzene indicated that enhancing denitrification alone was insufficient. Both benzene and o-xylene biodegraded significantly under iron-reducing conditions, but only after denitrification had removed other aromatics. For the trimethylbenzene isomers, 1,3,5-TMB biodegradation was found under denitrifying and then iron-reducing conditions. Biodegradation of 1,2,3-TMB or 1,2,4-TMB was slower under iron-reducing conditions. This study suggests that addition of excess ferric iron combined with limited nitrate has promise for in situ bioremediation of BTEX and TMB in the Borden aquifer and possibly for other sites contaminated by hydrocarbons. This study is the first to report 1,2,3-TMB biodegradation under strictly anaerobic condition. With the addition of 500 mg/L ethanol but without EA addition, ethanol and its main intermediate, acetate, were quickly biodegraded within 41 d with methane as a major product. Ethanol initially present at 5000 mg/L without EA addition declined slowly with the persistence of unidentified volatile fatty acids, likely propionate and butyrate, but less methane. In contrast, all ethanol disappeared with repeated additions of either nitrate or ferric iron, but acetate and unidentified intermediates persisted under iron-enhanced conditions. With the addition of 500 mg/L ethanol and nitrate, only minor toluene biodegradation was observed under denitrifying conditions and only after ethanol and acetate were utilized. The higher ethanol concentration (5000 mg/L) essentially shut down BTEX biodegradation likely due to high EA demand provided by ethanol and its intermediates. The negative findings for anaerobic BTEX biodegradation in the presence of ethanol and/or its biodegradation products are in contrast to recent research reported by Da Silva et al. [Da Silva, M.L.B., Ruiz-Aguilar, G.M.L., Alvarez, P.J.J., 2005. Enhanced anaerobic biodegradation of BTEX-ethanol mixtures in aquifer columns amended with sulfate, chelated ferric iron or nitrate. Biodegradation. 16, 105-114]. Our results suggest that the apparent conservation of high residual labile carbon as biodegradation products such as acetate makes natural attenuation of aromatics less effective, and makes subsequent addition of EAs to promote in situ BTEX biodegradation problematic. 相似文献
970.
Lopez-Espinosa MJ Kiviranta H Araque P Ruokojärvi P Molina-Molina JM Fernandez MF Vartiainen T Olea N 《Chemosphere》2008,73(6):967-971
Seventeen polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were quantified in adipose tissue samples of non-occupationally exposed women living in Southern Spain. Geometric mean levels of sum of congeners and WHO(PCDD/F)-TEQ(2005) were 410 and 17.9pgg(-1) fat, respectively. Among PCDDs, octachlorodibenzo-p-dioxin (OCDD) showed the highest concentration with a mean value of 265pgg(-1) fat, followed by 1,2,3,6,7,8-HxCDD (49.3pgg(-1) fat) and 1,2,3,4,6,7,8-HpCDD (45.2pgg(-1) fat). These three congeners were responsible for around 90% of the sum of all PCDD/F congeners in adipose tissue. The geometric mean 2,3,7,8-TCDD value was 1.87pgg(-1) fat. 2,3,4,7,8-PeCDF (8.43pgg(-1) fat) showed the highest concentration among the PCDFs, followed by 1,2,3,4,7,8-HxCDF (4.17pgg(-1) fat) and 1,2,3,6,7,8-HxCDF (3.28pgg(-1) fat), and these three congeners were responsible for 4% of the sum of all studied PCDD/F congeners in adipose tissue and 76% of the sum of ten PCDFs. 1,2,3,7,8,9-HxCDF was the only congener not quantified in any sample, while 1,2,3,4,7,8,9-HpCDF, 1,2,3,7,8-PeCDF, OCDF and 2,3,7,8-TCDF were found in 5, 16, 16 and 19 samples, respectively. All other congeners were quantifiable in all 20 samples. Congeners contributing most to the WHO(PCDD/F)-TEQ(2005) were 1,2,3,7,8-PeCDD (31.6%), 1,2,3,6,7,8-HxCDD (28.3%) and 2,3,4,7,8-PeCDF (14.6%). The body burden of log-transformed WHO(PCDD/F)-TEQ(2005) levels increased with age (B=0.02; 95% CI=0.01, 0.03; p=0.02). Although these adipose tissue PCDD/F levels are similar to previously published findings in Spain and other European countries, further research is needed to determine trends in the exposure of women to these chemical residues. 相似文献