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Fluorescence and bioluminescence analysis of sequential UV-biological degradation of p-cresol in water.

The photolysis and Penicillium tardum H-2 degradation of p-cresol in water containing humic acids was investigated by fluorescence and bioluminescence methods. Humic acids extracted from peat (the Vasuygan bog, Tomsk region of Russia) induce the phototransformation of p-cresol. The influence of humic acids on the phototransformation of p-cresol under different irradiation conditions was investigated. Comparison of the data on the KrCl* (lambda = 222 nm) and XeCl* (lambda = 308 nm) excilamps light showed that the most effective p-cresol degradation was observed with mercury lamp irradiation in the presence of humic acids.

Biodegradation, Environmental↗

Macrokinetic and quantitative microbial investigation on a bench-scale biofilter treating styrene-polluted gaseous streams.

We performed a macrokinetic and quantitative microbial investigation of a continuously operating bench-scale biofilter treating styrene-polluted gases. The device was filled with a mixture of peat and glass beads as packing medium and inoculated with the styrene-oxidizing strain, Rhodococcus rhodochrous AL NCIMB 13259. The experimental data of styrene and microbial concentrations, obtained at different biofilter heights, were used to evaluate the pollutant concentration profiles as well as the influence of styrene loading on biomass distribution along the packing medium. Styrene and biomass concentration profiles permitted detection of a linear relationship between the amount of biomass grown in a given section of the biofilter and that of pollutant removed, regardless of the operating conditions tested. Biomass development in the bed appeared to: depend linearly on pollutant concentration at an inlet styrene concentration of <0.10 g m(-3) in the gaseous stream; achieve a maximum value (7. 10(7) colony forming units per gram of packing material) within a wide styrene concentration range (0.10 to 1.0 g m(-3)); and fall sharply beyond this inhibition threshold. The process followed zeroth-order macrokinetics with respect to styrene concentration, which is consistent with zeroth-order microkinetics with either fully active or not fully active biofilm. The maximal volumetric styrene removal rate was found to be 63 g m(packing material) (-3) h(-1) for an influent pollutant concentration of 0.80 g m(-3) and a superficial gas velocity of 245 m h(-1).

Adsorption↗

Biofiltration of a mixture of volatile organic compounds on granular activated carbon.

The performance of a biofilter packed with Active Carbon (AC) was evaluated. The effluent (alcohol, ketones, esters, aromatic and chlorinated compounds) treated was a representative mixture of most common industrial emissions. To achieve a better knowledge of multicomponent adsorption mechanisms, and to underline the interest of inoculating AC, a control abiotic humidified filter had been operated in the same conditions as the biofilter. For a load of 110 g VOC m(-3) AC h(-1), after 55 days of operation, the removal efficiency was higher in the biotic than in the abiotic filter (85% vs 55%, respectively). Moreover, in the biofilter, at steady state, the elimination of all compounds was almost complete except for chlorinated compounds and p-xylene (removal efficiency of 25% and 64%, respectively). The microbial colonization of AC involved a decrease of the adsorption sites accessibility and enhanced the treatment of VOCs (volatile organic compounds) having a lower affinity for activated carbon. Moreover, while aromatic compounds and MIBK were eliminated along the overall height of the biofilter, pollutants with reduced affinity for AC, such as methanol, acetone, and halogenated compounds were only treated on the second half of the reactor. Thus, the affinity for activated carbon was an important parameter controlling the biodegradation process. Nevertheless, the use of AC as packing material in biofilters treating complex mixtures of VOCs is limited. Actually, similar removal efficiency could be reached, in the same conditions, for a biofilter packed with granular peat. Furthermore, for the biofilter packed with AC, the column height necessary to remove biodegradable compounds, with reduced affinity for the support, was important.

Adsorption↗

Detachment and emission of airborne bacteria in gas-phase biofilm reactors.

Three laboratory scale biofilters filled with different packing materials (peat and sieved sugarcane bagasse) and operating with different microbial cultures (allochthonous and autochthonous bacteria) were run and monitored in parallel to assess the emission rate of airborne bacteria in the biofiltration of benzene-contaminated air streams. The effect of the fluid dynamic and loading conditions on the rate of microbial emission in the air environment was investigated by performing continuous experiments at different inlet benzene concentrations and superficial gas velocities. The experiments prove that the concentration of airborne bacteria in the effluent air from lab-scale biofilters is only slightly higher than in the ambient air. The emission rate is not dependent on superficial gas velocity because of low shear stress exerted by the gas flow. On the other hand, the loading conditions have a strong effect on the emission rate, which increases with increasing growth and degradation rate, and different packing media show remarkably different behaviors.

Air Microbiology↗

Adsorption, absorption, and biological degradation of ammonia in different biofilter organic media.

A tailor-made apparatus called ammoniometer, which is a batch mode respirometer applied to the study of ammonia biodegradation in biofilter media, has been used to evaluate adsorption, absorption, and biodegradation in five different organic materials (compost, coconut fibre, bark, pruning wastes, and peat) obtained from full-scale biofilters in operation in several waste treatment plants. The results showed that absorption could be represented by a Henry's law linear equation, with values of the Henry coefficient significantly higher (from 1,866 to 15,320) than that of pure water (1,498). Adsorption data were successfully fitted to Langmuir and Freundlich isotherms and maximum adsorption capacity varies from 1.06 to 1.81 mg NH(3)/g dry media. Ammonia biodegradation rates for each organic material were also calculated. Biodegradation rates varied from 0.67 to 7.82 mg NH(3)/kg media/d depending on the material tested. The data obtained showed important differences in the behaviour of the biofilter organic media, which has important implications in the design and modelling of these systems.

Absorption↗

Kinetic studies on the yeast Phaffia rhodozyma.

The yeast Phaffia rhodozyma, a promising microbial producer of the carotenoid astaxanthin, was cultivated in batch and continuous processes in an agitated and aerated fermenter using an acid peat extract based culture medium. For the accelerated growth phase, the mean specific growth rate and doubling time were found to be 0.038 h-1, and 18.24 hours, respectively. The production of astaxanthin was found to be basically growth associated, the maximum concentrations of the pigment produced in batch culture and continuous cultivation being similar.

Biomass↗

Methods for assessing the toxicity of herbicides to submersed aquatic plants.

A new test design for the non-axenic submergent aquatic macrophytes Elodea canadensis Michx. and Myriophyllum spicatum L. has been developed for potential use in herbicide toxicity testing. For the non-axenic cultures, the best growth conditions were observed in the Elendt-M4 medium in which no growth of algae or bacteria was observed. Cuttings were placed in beakers containing only the artificial M4 medium or were planted in small beakers containing OECD (Organisation for Economic Cooperation and Development) sediment (5% peat, 75% sand, 20% kaolinite), which were then placed in larger vessels with the M4 medium. The plants were observed for main and secondary shoot length, biomass and root formation within 2-3 weeks of planting. Growth rates were calculated for total plant length and biomass. The variance between the replicates was low throughout the experiment [coefficient of variation (CV) < 26% for total plant length, and between 16 and 40% for biomass]. Relative growth rates based on total plant length were determined as 0.028 and 0.050 per day for M. spicatum in the systems containing M4 medium only and medium plus sediment respectively. Similar results were observed for E. canadensis, with relative growth rates of 0.26 and 0.073 per day in the two test systems. The root-shoot ratio at harvest was greater by a factor of 2-3 for E. canadensis in the M4 medium than in the system containing sediment. However, comparable ratios were observed for M. spicatum in the two test systems. Both growth in total plant length and growth in biomass of the two species have potential as measures of toxicity.

Culture Media↗

Influence of a Nonionic Surfactant (Triton X-100) on Contaminant Distribution between Water and Several Soil Solids.

The influence of a nonionic surfactant (Triton X-100) on the contaminant distribution coefficients in solid-water mixtures was determined for a number of relatively nonpolar compounds (contaminants) on several natural solids. The studied compounds consisted of BTEX (benzene, toluene, ethylbenzene, and p-xylene) and chlorinated pesticides (lindane, alpha-BHC, and heptachlor epoxide), which span several orders of magnitude in water solubility (S(w)); the solid samples comprised a bentonite, a peat, and two other soils, which cover a wide range of solid organic matter (SOM) content. The applied surfactant concentrations (X) ranged from below the (nominal) CMC to 2-3 times the CMC. For relatively water-soluble BTEX compounds, the distribution coefficients with surfactant (K(d)*) all exceeded those without surfactant (K(d)); the K(d)*/K(d) ratios increased with increasing S(w) from p-xylene to benzene on each solid at a given X, with increasing X for each compound on a solid, and with decreasing solid SOM content for each compound over the range of X studied. For the less-soluble pesticides, the K(d)*/K(d) ratios exhibited a large increase with X for bentonite, a marginal change (increase or decrease) for a soil of 2.4% SOM, and a moderate-to-large decrease for two soils of 14.8% and 86.4% SOM. These unique observations were rationalized in terms of the properties of the compound, the amount of surfactant sorbed on the solid, the enhanced solubilization of the compound by surfactant in water, and the relative effects of the surfactant when adsorbed on minerals and when partitioned into SOM. Copyright 2000 Academic Press.

Journal Article↗

On the adsorption/oxidation of hydrogen sulfide on activated carbons at ambient temperatures.

Activated carbons of various origins (bituminous coal, wood, coconut shells, and peat) were studied as adsorbents of hydrogen sulfide. Before the experiments the surface of the adsorbents was characterized by using the sorption of nitrogen, Boehm and potentiometric titrations, thermal analysis, and FTIR. The adsorbents were chosen to differ in their surface areas, pore volumes, and surface acidities. To broaden the spectrum of surface acidity, carbons were oxidized by using nitric acid and ammonium persulfate. After hydrogen sulfide adsorption the species present on the surface were analyzed using thermal analysis, ion chromatography, and elemental analysis. The H(2)S breakthrough capacity tests showed that the performances of different carbons differ significantly. For a good performance of carbons as hydrogen sulfide adsorbents a proper combination of surface chemistry of carbon and porosity is needed. It was demonstrated that a more acidic environment promotes the formation of sulfur oxides and sulfuric acid despite yielding small H(2)S removal capacities. On the other hand, a basic environment favors the formation of elemental sulfur (sulfur radicals) and yields high capacities. The presence of a sufficient amount of water preadsorbed on the carbon surface to facilitate dissociation also plays an important role in the process of H(2)S adsorption/oxidation. The results showed that there is a critical value in carbon surface acidity, which when exceeded results in a negligible hydrogen sulfide breakthrough capacity. This is consistent with the mechanism of H(2)S adsorption on unmodified carbons, where the rate-limiting step is the reaction of adsorbed hydrogen sulfide ion with dissociatively adsorbed oxygen. When the acidity is expressed as pH, its value should be higher than 5 to ensure the effective removal of hydrogen sulfide from the gas phase. Study of carbon regeneration using water washing and heat treatment showed that the adsorbents can be regenerated to about 40% of their initial capacity.

Journal Article↗

Selective dephasing of OH and NH proton magnetization based on (1)H chemical-shift anisotropy recoupling.

A method for selectively suppressing the signals of OH and NH protons in (1)H combined rotation and multiple-pulse spectroscopy (CRAMPS) and in (1)H-(13)C heteronuclear correlation (HETCOR) solid-state NMR spectra is presented. It permits distinction of overlapping CH and OH/NH proton signals, based on the selective dephasing of the magnetization of OH and NH protons by their relatively large (1)H chemical-shift anisotropies. For NH protons, the (14)N-(1)H dipolar coupling also contributes significantly to this dephasing. The dephasing is achieved by a new combination of heteronuclear recoupling of these anisotropies with (1)H homonuclear dipolar decoupling. Since the 180 degrees pulses traditionally used for heteronuclear dipolar and chemical-shift anisotropy recoupling would result in undesirable homonuclear dephasing of proton magnetization, instead the necessary inversion of the chemical-shift Hamiltonian every half rotation period is achieved by inverting the phases of all the pulses in the HW8 multiple-pulse sequence. In the HETCOR experiments, carefully timed (13)C 180 degrees pulses remove the strong dipolar coupling to the nearby (13)C spin. The suppression of NH and OH peaks is demonstrated on crystalline model compounds. The technique in combination with HETCOR NMR is applied to identify the CONH and NH-CH groups in chitin and to distinguish NH and aromatic proton peaks in a peat humin.

Journal Article↗

Magnetic susceptibility effects on 13C MAS NMR spectra of carbon materials and graphite.

13C high-resolution solid-state nuclear magnetic resonance (NMR) was employed to study carbon materials prepared through the thermal decomposition of four different organic precursors (rice hulls, endocarp of babassu coconut, peat, and PVC). For heat treatment temperatures (HTTs) above about 600 C, all materials presented 13C NMR spectra composed of a unique resonance line associated with carbon atoms in aromatic planes. With increasing HTT a continuous broadening of this resonance and a diamagnetic shift in its central frequency were verified for all samples. The evolution of the magnitude and anisotropy of the magnetic susceptibility of the heat-treated carbon samples with HTT explains well these findings. It is shown that these results are better understood when a comparison is made with the features of the 13C NMR spectrum of polycrystalline graphite, for which the magnetic susceptibility effect is also present and is much more pronounced.

Anisotropy↗

Extraction of ribosomal RNA from soil for detection of Frankia with oligonucleotide probes.

Sequences of 16S rRNA of the nitrogen-fixing Frankia strain Ag45/Mut15 and the ineffective Frankia strain AgB1.9 were used to design a genus-specific oligonucleotide probe. Hybridization experiments of this Frankia probe and a second probe, specific for Nif+-Frankia strains only, were used to detect Frankia specific target sequences in RNA isolations from soil. A method is described for direct isolation of RNA from a loamy soil and a peat. Yields of about 10 ng RNA/g wet soil are obtained without detectable contamination with humic acids. Isolation of RNA after initial extraction of bacteria from soil resulted in significantly lower RNA yields, compared to the direct isolation procedure. Hybridization with both probes against rRNA isolations from Frankia-containing soil could detect target sequences within RNA isolations from 1 g wet soil with an estimated detection limit of 10(4) cells.

Actinomycetales↗

The effect of sulfate and nitrate on methane formation in a freshwater sediment.

A freshwater sediment from a ditch of a peat grassland near Zegveld (Province of Utrecht, The Netherlands) was investigated for its potential methanogenic and syntrophic activity and the influence of sulfate and nitrate on these potential activities. Methanogenesis started after a 10 days lagphase. After 35-40 days aceticlastic methanogens were sufficiently enriched to cause a net decrease of acetate. In the presence of sulfate methane formation was only slightly affected. The addition of nitrate led to an outcompetition of aceticlastic methanogens by nitrate reducers. When inorganic electron acceptors were absent, substrates like propionate and butyrate were converted by syntrophic methanogenic consortia. Addition of inorganic electron acceptors resulted in an outcompetition of the syntrophic propionate and butyrate degrading consortia by the sulfate and nitrate reducers.

Acetates↗

Burrowing behavior in wild house mice: variation within and between populations.

Burrowing behavior was assessed on 120 lab-reared house mice (Mus domesticus) derived from five geographic populations representing a north-south cline along the east coast of the United States. Mice were placed individually into Plexiglas containers filled with sand and peat moss, and their burrows were excavated 24 h later. Seven measures were taken and reduced by principal-components analysis to two factors for further analysis. Marked differences existed within, but not between populations, and members of full-sib families built qualitatively and quantitatively similar burrows. The lack of a geographic cline and the apparent high heritability of burrowing behavior do not lend support to its use as a major thermoregulatory adaptation.

Animals↗

Silver uptake by Agaricus bisporus from an artificially enriched substrate.

The champignon mushroom Agaricus bisporus was cultivated on compost (wheat and rye straw, hens' manure, gypsum, urea and peat) artificially fortified with silver nitrate added at four different concentrations (0.01, 0.1, 1.0 and 10.3 mg/kg) and 0 mg/kg (control) on a dry weight basis. The method of measurement was flame atomic absorption spectrophotometry after dry ashing of the samples at 420 degrees C and dissolving the residue in 1 M nitric acid. The highest concentration of silver, reaching between 120 +/- 30-150 +/- 36 mg/kg on a dry weight basis, was observed in fruit bodies grown on the most contaminated substrate containing 10.3 mg added Ag/kg dry weight. The silver concentration in caps/stalks/whole fruit bodies of A. bisporus was positively correlated (r = 0.72; P < 0.001) with an increasing level of fortification of the substrate. The bioconcentration factor (BCF) of silver in caps/stalks/whole fruit bodies of A. bisporus was inversely correlated (-0.44 < r < -0.36; 0.001 < p < 0.01) with the silver concentration of the contaminated substrate. The highest silver BCF value of 120-230 has been observed in caps and stalks of mushrooms grown on a substrate enriched with 0.01 mg Ag/kg dry weight. Silver ion added to the substrate in concentrations up to 10.3 mg/kg on a dry weight basis exhibited no observable toxic effect against the mycelial growth and fruiting of A. bisporus.

Agaricus↗

Remediation of an old landsfill site: soil analysis, leachate quality and gas production.

The Baltic Sea Region has a large number of landfills that need remediation after care routines and control, in order to avoid future emissions to the environment and to fulfil the demands in the EU Waste Council Directive on the landfill of waste. Based on the Måsalycke test screening, an excavation of whole or of parts of the landfill can be seen as a potential measure for some of the old landfills. The material excavated in the test was screened into the fractions: < 18 mm, 18-50 mm and > 50 mm. The coarsest fraction (> 50 mm) contained 50% wood and paper. The medium-sized fraction (18-50 mm) contained stones and indefinable soil-like material, while the fine fraction contained peat-like material with some other small waste components. The spectral analysis of heavy metals indicated only high concentrations of zinc and there was no significant difference between the fine and the medium-sized fractions. The medium sized and the unsorted fraction was moisturized and refilled into the pit. The methane content in the landfill gas from the pit was 50-57% in the sorted material with a flow of 8-17 l/min and 38-57% in the unsorted fraction with a flow of 2-13 l/min during the first 1.5 year. The Måsalycke landfill is in the methanogenic phase and leachate concentrations are normal. Landfill mining can be used to prolong the landfill lifetime and/or used as a tool for remedial actions in contaminated sites.

Conservation of Natural Resources↗

The comparison study of compost and natural organic matter samples.

Sewage sludge is a serious problem facing modern wastewater treatment plants. One of the methods to safely utilize the sludge is through composting and the agricultural use of the final product. In this study the compost samples from municipal sewage sludge are compared to the natural, rich in organic matter samples. Based on physicochemical properties of the material, the maturity indices are obtained to evaluate the quality of organic matter and estimate the similarities between the samples. The study shows that one-dimensional analysis like that based on maturity indices does not provide satisfactory answers concerning the nature of such complex materials. The data set of the analysis naturally possesses a multidimensional character so that the employment of advanced chemometric techniques like cluster analysis show a number of features which were hidden within the 'data flood'. The major conclusion of this work is that the compost from sewage sludge is similar to peat in the significance of the properties of the organic matter. Moreover, the organic matter of agricultural soil, which is most stable and has been naturally matured over a long period of time, differs substantially from the other samples.

Agriculture↗

A novel pmoA lineage represented by the acidophilic methanotrophic bacterium Methylocapsa acidiphila [correction of acidophila] B2.

A fragment of the functional gene pmoA, which encodes the active-site polypeptide of particulate methane monooxygenase (pMMO), was PCR-amplified from DNA of the recently described acidophilic methanotrophic bacterium Methylocapsa acidiphila [corrected] B2. This methanotroph was isolated from an acidic Sphagnum peat bog and possesses a novel type III arrangement of intracytoplasmic membranes. Comparative sequence analysis revealed that the inferred peptide sequence of pmoA of Methylocapsa acidiphila [corrected] B2 belongs to a novel PmoA lineage. This lineage was only distantly related to the PmoA sequence cluster of type II methanotrophs, with identity values between 69.5% and 72%. The identity values between the PmoA of Methylocapsa acidiphila [corrected] B2 and PmoA sequences of type I methanotrophs ranged from 55.5 to 68%. However, the PmoA of this acidophilic methanotroph was more closely affiliated with the inferred peptide sequences of pmoA clones retrieved from various acidic upland soils showing atmospheric methane consumption. The PmoA identity values with these clones were 79.5-81%. Nonetheless, the apparent affinity for methane exhibited by Methylocapsa acidiphila [corrected] B2 was 1-2 microM, which is similar to values measured in other methanotrophic bacteria. This finding suggests that the pMMO of Methylocapsa acidiphila [corrected] B2 is not a novel enzyme specialized to have a high affinity for methane and that apparent "high-affinity" methane uptake is either the result of particular culture conditions or is performed by another pMMO type.

Alcohol Oxidoreductases↗