Community Refinery Wastewater Photodegradation by Fe-Doped TiO<Subscript>2</Subscript> Films

Photocatalytic treatment of real community wastewater using Fe-doped TiO₂ nanofilm was prepared by modified sol-gel method together with a simple dip-coating technique. The process was investigated in a home-made batch photoreactor. The as-prepared nanocomposite film was characterized by UV-Vis diffuse, XRD, BET, and Fe-SEM analysis. The poultry processing wastewater was collected from Nakhonsawan Municipality. Subsequently, the photocatalytic treatment of the wastewater was performed using a home-made photoreactor operated in batch mode to demonstrate the effects of Fe-dopant concentration with various layer numbers. The catalysts were irradiated using four lamps of 15 W power that emitted visible light and performed at room temperature. The samples were collected every 15 min and analyzed for biochemical oxygen demand (BOD) and chemical oxygen demand (COD) removal efficiency compared to pure TiO₂ nanofilm and direct photolysis. From the results, the mixture of rutile and anatase was obtained with the maximum specific surface area of 150.12 mg²/g and the average particle size of 39.95 nm for 3 layers of 0.15% wt/v Fe-doped TiO₂. The BOD and COD value at 90 min time treatment was presented to be 8.87 and 32 mg L^?1, respectively, in the presence of 0.15% wt/v Fe-doped TiO₂ film photocatalysts. Moreover, atomic absorption spectrometric result ensured that no Ti contamination was detected in all parts of plants after watering by the treated water. Hence, the photocatalytic treatment markedly improved the quality of the community wastewater.     

Photocatalytic Removal of the Antibiotic Cefotaxime on TiO<Subscript>2</Subscript> and ZnO Suspensions Under Simulated Sunlight Radiation

This study presents the main results about the removal of the antibiotic cefotaxime (CTX) under simulated sunlight radiation using heterogeneous photocatalysis with titanium dioxide (TiO₂) and zinc oxide (ZnO) in aqueous solutions. The effects of pH and catalyst initial load on pollutant removal were assessed considering the response surface methodology and a central composite circumscribed experimental design, which allowed to determine the optimized conditions that lead to a higher substrate elimination. Experimental results indicated that evaluated parameters have a significant effect on antibiotic removal in both TiO₂ and ZnO suspensions. In addition, the role of photogenerated holes, hydroxyl, and superoxide anion radicals on CTX degradation was evaluated to clarify the reaction mechanism. Finally, analysis of the dissolved organic carbon content in solutions and the antibacterial activity of treated samples showed that photocatalytic treatments were able to reduce a considerable portion of the organic matter present in the systems and its antimicrobial activity.     

Visible-Light-Driven Photocatalytic N-Doped TiO<Subscript>2</Subscript> for Degradation of Bisphenol A (BPA) and Reactive Black 5 (RB5) Dye

Bisphenol A (BPA) and reactive black 5 (RB5) dye are among the most persistent and non-biodegradable contaminants in water which require an urgent need for the development of effective removal method. The ubiquitous existence of both contaminants could interfere with the human health and aquatic environmental balance. Photocatalytic process as one of advanced oxidation processes (AOPs) has shown high performance for degradation of organic compounds to the harmless materials under sensible condition. Therefore, this study aims to develop a visible-light-driven photocatalyst that can efficiently degrade BPA and RB5 present in household water. N-doped TiO₂ were successfully synthesized via simple and direct sol–gel method. The prepared TiO₂ nanoparticles were characterized by field emission scanning microscope (FE-SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR), and Brunauere Emmette Teller (BET) analysis. The incorporation of nitrogen in TiO₂ lattice exhibited excellent optical responses to visible region as revealed by UV–Vis–NIR spectroscopy absorption capability at 400–600 nm. The photocatalytic activity of the N-doped TiO₂ nanoparticles was measured by photocatalytic degradation of BPA and RB5 in an aqueous solution under visible-light irradiations. Degradation of BPA and RB5 was 91.3% and 89.1%, respectively after 360 min illumination. The degradation of BPA and RB5 by N-doped TiO₂ was increased up to 89.8% and 88.4%, respectively under visible-light irradiation as compared to commercial TiO₂ P25. This finding clearly shows that N-doped TiO₂ exhibits excellent photocatalytic degradation of BPA and RB5 under visible irradiation, hence have a promising potential in removing various recalcitrant contaminants for water treatment to fulfill the public need to consume clean water.

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Improved Photodegradation Efficiency of 2,4-DCP Through a Combined Q<Subscript>3</Subscript>Fe(III)-Decorated Porous g-C<Subscript>3</Subscript>N<Subscript>4</Subscript>/H<Subscript>2</Subscript>O<Subscript>2</Subscript> System

Graphitic carbon nitride (g-C₃N₄) is a photocatalyst with wide application in removal of organic pollutants. In this study, we designed a porous g-C₃N₄ (p-g-C₃N₄)/8-quinolinolato iron(III) (Q₃Fe)/H₂O₂ system to enhance the organic pollutant removal efficiency by combining photocatalysis and Fenton interaction under neutral condition. The p-g-C₃N₄ was prepared through a two-step thermal oxidation reaction. Afterwards, Q₃Fe-coupled p-g-C₃N₄ was prepared by an impregnating method. The 2,4-dichlorophenol (2,4-DCP) photodegradation ratio and decomposition rate of the p-g-C₃N₄/Q₃Fe/H₂O₂ system are approximately 5 and 18 times as high as those of individual p-g-C₃N₄ system, respectively. Besides, its degradation rate is 4.3 times as high as that in the p-g-C₃N₄/H₂O₂ system. Meanwhile, Q₃Fe/g-C₃N₄ also exhibits higher activity than individual p-g-C₃N₄ in 2,4-DCP photo-decomposing. On the basis of the results of the radical trapping experiments and the Fe(II) concentration in different systems, the synergistic effect between photocatalysis and Fenton reaction is vital for the efficient pollutant degradation. The coupled system combining p-g-C₃N₄ with Q₃Fe and H₂O₂ shows potential for efficient treatment of recalcitrant organic pollutants. The combined system in this work indicated a new idea for the decomposition of organic pollutants.     

TiO<Subscript>2</Subscript> photocatalytic degradation of 4-chlorobiphenyl as affected by solvents and surfactants

Purpose  

TiO₂ photocatalytic degradation of 4-chlorobiphenyl (PCB3) in aqueous solution under UV irradiation was investigated as affected by different environmental factors, including initial PCB3 concentration, TiO₂ content, UV intensity, H₂O₂ concentration, cosolvents, and surfactants.     

Effective Removal of Toxic Heavy Metal Ions from Aqueous Solution by CaCO<Subscript>3</Subscript> Microparticles

Heavy metals are a common contaminant in water supplies and pose a variety of serious health risks to nearby human populations. A promising approach to heavy metal decontamination is the sequestration of heavy metal ions in porous materials; however, current technologies involve materials which can be difficult to synthesize, are high-cost, or are themselves potentially toxic. Herein, we demonstrate that rapidly synthesized calcium carbonate (CaCO₃) microparticles can effectively remove high quantities of Pb²⁺, Cd²⁺, and Cu²⁺ ions (1869, 1320, and 1293 mg per gram of CaCO₃ microparticles, respectively) from aqueous media. The CaCO₃ microparticles were characterized with powder X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and Brunauer–Emmett–Teller (BET) N₂ sorption–desorption. It was found that the Ca²⁺ ions of the microparticles were replaced by the heavy metal ions, leading to partially recrystallized nanoparticles of new compositional phases such as cerussite (PbCO₃). The adsorption, surface dissolution/re-precipitation, and nucleation/crystal growth mechanisms were determined by investigating the Ca²⁺ released, along with the changes to particle morphology and crystal structure. Importantly, this study demonstrates that the porous CaCO₃ microparticles performed well in a system with multiple heavy metal ion species: 100% of Cu²⁺, 97.5% of Pb²⁺, and 37.0% Cd²⁺ were removed from an aqueous solution of all cations with initial individual metal concentrations of 50 mg/L and 1.5 g/L of CaCO₃ microparticles. At this concentration, the CaCO₃ microparticles significantly outperformed activated carbon. These results help to establish CaCO₃ microparticles as a promising low-cost and scalable technology for removing heavy metal ions from contaminated water.

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Visible-Light-Induced Photocatalytic Degradation of PAH-Contaminated Soil and Their Pathways by Fe-Doped TiO<Subscript>2</Subscript> Nanocatalyst

The aim of the present study was to establish the photocatalytic efficiency of Fe-doped TiO₂ nanocatalysts toward polycyclic aromatic hydrocarbons (PAHs), which were phenanthrene, anthracene, and fluoranthene, contaminated soil under visible irradiation. The morphology, phase, and particle size of the prepared nanocatalyst have been studied as a first mention in literature. The photoresponse of the TiO₂ extends from UV region to the visible region was proved by the diffuse reflectance spectrophotometry (DRS). The surface area is greatly increased though the Fe-doped TiO₂ compared with the bare TiO₂. The pH value of the media showed the beneficial to PAH absorption on the Fe-doped TiO₂ under the alkaline condition due to the surface catalyst possesses much negative charge, which is increase in percentage of PAH degradation. Based on GC-MS study, the mechanism of photoactivity of the selected PAHs involves hydroxylation, ring opening, and rearrangement reactions. The main intermediates of PAH photodegradation were found to be 9-octadecanoic acid, heptadecane, octadecane, cyclohexane (1-hexadecylheptadecyl), and 15-hydroxypentadecanoic acid.     

Efficient Photocatalytic Reduction of CO<Subscript>2</Subscript> Present in Seawater into Methanol over Cu/C-Co-Doped TiO<Subscript>2</Subscript> Nanocatalyst Under UV and Natural Sunlight

Photocatalytic reduction of CO₂ in seawater into chemical fuel, methanol (CH₃OH), was achieved over Cu/C-co-doped TiO₂ nanoparticles under UV and natural sunlight. Photocatalysts with different Cu loadings (0, 0.5, 1, 3, 5, and 7 wt%) were synthesized by the sol–gel method and were characterized by XRD, SEM, UV–Vis, FTIR, and XPS. Co-doping with C and Cu into TiO₂ remarkably promoted the photocatalytic production of CH₃OH. This improvement was attributed to lowering of bandgap energy, specific catalytic effect of Cu for CH₃OH formation, and the minimization of photo-generated carrier recombination. Co-doped TiO₂ with 3.0 wt% Cu was found to be the most active catalyst, giving a maximum methanol yield rate of 577 μmol g-cat^?1 h^?1 under illumination of UV light, which is 5.3-fold higher than the production rate over C-TiO₂ and 7.4 times the amount produced using Degussa P25 TiO₂. Under natural sunlight, the maximum rate of the photocatalytic production of CH₃OH using 3.0 wt% Cu/C-TiO₂ was found to be 188 μmol g-cat^?1 h^?1, which is 2.24 times higher than that of C-TiO₂, whereas, no CH₃OH was observed for P25.     

Removal of Cationic Dyes,Heavy Metal Ions,and CO<Subscript>2</Subscript> Capture by Adsorption on Mesoporous Silica HMS

Mesoporous silica with wormhole framework structure (HMS-OH) and its amine-functionalized material (HMS-NH₂) were prepared through an electrically neutral assembly pathways, post-grafting process of 3-aminopropyltriethoxysilane (APTES), respectively. Their adsorption behaviors toward cationic dyes as well as heavy metal ions in aqueous system and the capture capacities for CO₂ molecules all have been investigated. As-synthesized HMS-OH showed a high removal efficiency and rapid sorption rate to cationic dyes because of large surface area and versatile pore structure. HMS-NH₂ exhibited better heavy metal ions and more CO₂ gas sorption capacities due to the intrinsic property of amine groups grafted on the surface. The adsorption isotherms of methylene blue (MB) onto HMS-OH, Cu(II) onto HMS-NH₂ were fitted with Langmuir model and kinetic processes followed well the pseudo-second order pattern. There results revealed that both HMS-OH and HMS-NH₂ had a potential application in the treatment of cationic dyes, heavy metal ions, and greenhouse gas CO₂.     

Soil N<Subscript>2</Subscript>O emissions and N<Subscript>2</Subscript>O/(N<Subscript>2</Subscript>O+N<Subscript>2</Subscript>) ratio as affected by different fertilization practices and soil moisture

The objective of this work was to evaluate the effect of the chemical nature and application frequency of N fertilizers at different moisture contents on soil N₂O emissions and N₂O/(N₂O+N₂) ratio. The research was based on five fertilization treatments: unfertilized control, a single application of 80 kg ha⁻¹ N-urea, five split applications of 16 kg ha⁻¹ N-urea, a single application of 80 kg ha⁻¹ N–KNO₃, five split applications of 16 kg ha⁻¹ N–KNO₃. Cumulative N₂O emissions for 22 days were unaffected by fertilization treatments at 32% water-filled pore space (WFPS). At 100% and 120% WFPS, cumulative N₂O emissions were highest from soil fertilized with KNO₃. The split application of N fertilizers decreased N₂O emissions compared to a single initial application only when KNO₃ was applied to a saturated soil, at 100% WFPS. Emissions of N₂O were very low after the application of urea, similar to those found at unfertilized soil. Average N₂O/(N₂O+N₂) ratio values were significantly affected by moisture levels (p = 0.015), being the lowest at 120% WFPS. The N₂O/(N₂O+N₂) ratio averaged 0.2 in unfertilized soil and 0.5 in fertilized soil, although these differences were not statistically significant.     

Influence of Biochar Addition on the Denitrification Process and N<Subscript>2</Subscript>O Emission in Cd-Contaminated Soil

The aim of this study was to investigate the effect of biochar addition on the denitrification process and N₂O emission in Cd-contaminated soil. Four different biochars, i.e., dairy manure and rice straw pyrolyzed at 350 and 550 °C, respectively, were added into a Cd-contaminated soil and incubation experiments were conducted for 8 weeks. Results showed that Cd had an inhibitory effect on denitrifying reductase enzymes and reduced the abundance of functional genes. On the contrary, amendment with the biochars increased denitrifying enzyme activity and gene abundance, and thus, enhanced the denitrification process. Labile carbon (C) in the biochar-amended soil, which was calculated based on the two-pool exponential model, was the key factor to facilitate this process. As a less important factor, elevated soil pH by biochar addition also increased denitrifying activity as well as the nosZ abundance. Decrease of Cd bioavailability by the biochar addition was beneficial to the denitrification process. Addition of the biochars with higher amount of NO₃ ^?-N, especially the rice straw-derived biochars, increased cumulative N₂O emission by more than ten times relative to the Cd-contaminated soil. With the great amount of labile C and NO₃ ^?-N, the treatment of biochars prepared at 350 °C released the larger amount of CO₂ and N₂O than other treatments. The biochar addition could totally release the heavy metal stress and restore the Cd-contaminated soil in terms of bacterial community.     

Reducing CH<Subscript>4</Subscript> and CO<Subscript>2</Subscript> emissions from waterlogged paddy soil with biochar

Purpose  

A potential means to diminish increasing levels of CO₂ in the atmosphere is the use of pyrolysis to convert biomass into biochar, which stabilizes the carbon (C) that is then applied to soil. Before biochar can be used on a large scale, especially in agricultural soils, its effects on the soil system need to be assessed. This is especially important in rice paddy soils that release large amounts of greenhouse gases to the atmosphere.     

Preparation of Highly Efficient CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/Zn<Subscript>2</Subscript>SnO<Subscript>4</Subscript> Composite Photocatalyst for the Degradation of Rhodamine B Dye from Aqueous Solution

CoFe₂O₄/Zn₂SnO₄ composite was synthesized using a simple two-step process and applied as a novel-efficient photocatalyst for the rhodamine B degradation from aqueous solution. Characterization techniques such as X-ray diffraction (XRD), N₂ adsorption-desorption isotherms, scanning electron microscopy (SEM), EDS analysis, and diffuse reflectance spectroscopy were employed in order to investigate the physical and chemical properties of composite. Higher values of the specific surface area, pore volume and diameter, and a smaller band-gap energy promoted a greater catalytic activity of CoFe₂O₄/Zn₂SnO₄ composite when compared to Zn₂SnO₄. A rapid decolorization of dye solution was observed at 40 min of reaction using the CoFe₂O₄/Zn₂SnO₄ catalyst, being 2.5 times faster than the Zn₂SnO₄ alone. Therefore, the CoFe₂O₄/Zn₂SnO₄ composite shows extraordinarily high photocatalytic activity toward the degradation of rhodamine B dye from aqueous solution.     

Effect of CO<Subscript>2</Subscript> on nitrification and immobilization of NH<Subscript>4</Subscript><Superscript>+</Superscript>-N

A laboratory incubation experiment was conducted to demonstrate that reduced availability of CO₂ may be an important factor limiting nitrification. Soil samples amended with wheat straw (0%, 0.1% and 0.2%) and (¹⁵NH₄)₂SO₄ (200 mg N kg^–1 soil, 2.213 atom% ¹⁵N excess) were incubated at 30±2°C for 20 days with or without the arrangement for trapping CO₂ resulting from the decomposition of organic matter. Nitrification (as determined by the disappearance of NH₄⁺ and accumulation of NO₃^–) was found to be highly sensitive to available CO₂ decreasing significantly when CO₂ was trapped in alkali solution and increasing substantially when the amount of CO₂ in the soil atmosphere increased due to the decomposition of added wheat straw. The co-efficient of correlation between NH₄⁺-N and NO₃^–-N content of soil was highly significant (r =0.99). During incubation, 0.1–78% of the applied NH₄⁺ was recovered as NO₃^– at different incubation intervals. Amendment of soil with wheat straw significantly increased NH₄⁺ immobilization. From 1.6% to 4.5% of the applied N was unaccounted for and was due to N losses. The results of the study suggest that decreased availability of CO₂ will limit the process of nitrification during soil incubations involving trapping of CO₂ (in closed vessels) or its removal from the stream of air passing over the incubated soil (in open-ended systems).     

Solar Photocatalysis Using Fixed-Film TiO<Subscript>2</Subscript> for Microcystins from Colonial <Emphasis Type="Italic">Microcystis aeruginosa</Emphasis>

Microcystins (MCs) are endotoxins produced by cyanobacteria in freshwaters globally. With known potential for human health risks, rapid and effective treatment methods are needed for MCs. Previous studies have shown photocatalysis can achieve rapid half-lives with UV lamps and slurries of TiO₂. In this experiment, rates and extents of solar photocatalysis of MCs were measured using bench-scale reactors with fixed films of TiO₂ for solutions with a range of cellular:aqueous MC ratios. Since cellular MCs can be removed physically, photocatalysis rates were measured following sand filtration to discern the extent of MC removal post-filtration. Since UV energy drives photocatalysis using TiO₂, rates of removal were calculated as a function of cumulative UV insolation and time. For water containing < 10% aqueous MC, filtration removed 90% of total MC, and the subsequent photocatalysis half-life was 0.37 MJ/m² (or 111 min). For water with ~?50% aqueous MCs, filtration removed 52% of the total MCs, and the average half-life for photocatalysis was 0.38 MJ/m² (or 138 min). For the >?90% aqueous MC treatment, filtration removed 0% MCs, and the photocatalysis half-life for MCs was 0.37 MJ/m² (or 135 min). Previous studies have used clarified waters; however, results from this study are likely representative of scenarios with waters containing confounding water characteristics and use of solar light for UV, as anticipated in developing countries with less advanced water treatment methods. Photocatalysis is a rapid and effective process for decreasing concentrations of MCs and could be useful for mitigating risks from MC exposures in drinking water.     

Photocatalytic Efficiency of TiO<Subscript>2</Subscript> Supported on Raw Red Clay Disks to Discolour Reactive Red 141

In this work, disks containing different amount of the TiO₂ precursor impregnated on the raw red clay were produced. The disks were obtained by pressing in metal template and subsequently calcined at 500 °C. The raw clay was used as rigid support to fix the TiO₂. The materials were characterized by X-ray diffraction, diffuse reflectance spectroscopy, N₂ adsorption-desorption (BET and BJH), scanning electron microscopy, and Fourier transform infrared (FTIR) spectroscopy. The ability of disks to produce superoxide and hydroxyl radicals after photoexcitation with UV irradiation was monitored by EPR. The catalytic efficiency was evaluated by the Reactive Red 141 dye discoloration under artificial UV light and sunlight. The reaction parameters such as concentration of RR-141 and irradiation source were evaluated. The results showed that the disks were able to decolorize 97.5% under sunlight at 60 min. The disks were also efficient in the discoloration until the tenth cycle, resulting in discoloration values near the initial cycles. Additionally, the dye fragments produced in cleavage of molecule during the reaction were evaluated by LC/MS-MS.

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N<Subscript>2</Subscript>O,CO<Subscript>2</Subscript>, Production,and C Sequestration in Vineyards: a Review

Even if it is less polluting than other farm sectors, grape growing management has to adopt measures to mitigate greenhouse gas (GHG) emissions and to preserve the quality of grapevine by-products. In viticulture, by land and crop management, GHG emissions can be reduced through adjusting methods of tillage, fertilizing, harvesting, irrigation, vineyard maintenance, electricity, natural gas, and transport until wine marketing, etc. Besides CO₂, nitrous oxide (N₂O) and methane (CH₄), released from fertilizers and waste/wastewater management are produced in vineyards. As the main GHG in vineyards, N₂O can have the same harmful action like large quantities of CO₂. Carbon can be found in grape leaves, shoots, and even in fruit pulp, roots, canes, trunk, or soil organic matter. C sequestration in soil by using less tillage and tractor passing is one of the efficient methods to reduce GHG in vineyards, with the inconvenience that many years are needed for detectable changes. In the last decades, among other methods, cover crops have been used as one of the most efficient way to reduce GHG emissions and increase fertility in vineyards. Even if we analyze many references, there are still limited information on practical methods in reducing emissions of greenhouse gases in viticulture. The aim of the paper is to review the main GHG emissions produced in vineyards and the approached methods for their reduction, in order to maintain the quality of grapes and other by-products.     

Solar Decolorization of Methylene Blue by Magnetic MgFe<Subscript>2</Subscript>O<Subscript>4</Subscript>-MWCNT/Ag<Subscript>3</Subscript>VO<Subscript>4</Subscript> Visible Active Photocatalyst

MgFe₂O₄-MWCNT/Ag₃VO₄ photocatalyst was prepared for benefiting the visible region of solar spectrum. Prepared catalyst was characterized by using scanning electron microscope (SEM), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDX). Photocatalytic activity was measured by methylene blue (MB) decolorization under visible light obtained from a 105-W tungsten light bulb. Dye decolorization and its kinetics were followed up by means of a UV-vis spectrophotometer. Kinetic model of decolorization was found to be compatible with first-order kinetics. The effects of pH and concentration of MB solution on the decolorization efficiency were determined. Low and high pH conditions were found to be more effective in increasing the MB decolorization yield and rate. On the other hand, due to the low transparency of concentrated MB solutions, an increase on decolorization time and a lowering in decolorization yield were encountered. Thanks to the magnetic MgFe₂O₃ nanoparticles, 96% of the catalyst could be recovered by a simple magnetic bar. It was observed that simulated wastewater containing MB was also successfully decolorized showing that visible region-sensitive MgFe₂O₄-MWCNT/Ag₃VO₄ photocatalyst can be benefited as a potential, efficient, and reusable material for the removal organic pollutants in aquatic environment.     

Soil nitrogen mineralization and fate of (<Superscript>15</Superscript>NH<Subscript>4</Subscript>)<Subscript>2</Subscript>SO<Subscript>4</Subscript> in field-incubated soil in a hardwood plantation of subtropical Australia: the effect of mulching

Background, aim, and scope  

Mulching is frequently used to overcome the drought problem in hardwood plantations that are increasingly being established in lower rainfall areas of Queensland, Australia because of increasing land values. In addition to soil water content, soil nitrogen (N) availability is another critical determinant of plantation productivity in these areas. The purpose of this study was to understand how soil mineral N dynamics, in situ N mineralization, and the fate of fertilized N would be affected by mulching during the early establishment of hardwood plantations.     

Response of CH<Subscript>4</Subscript> oxidation and methanotrophic diversity to NH<Subscript>4</Subscript><Superscript>+</Superscript> and CH<Subscript>4</Subscript> mixing ratios

Methane oxidising activity and community structure of 11, specifically targeted, methanotrophic species have been examined in an arable soil. Soils were sampled from three different field plots, receiving no fertilisation (C), compost (G) and mineral fertiliser (M), respectively. Incubation experiments were carried out with and without pre-incubation at elevated CH₄ mixing ratios (100 ml CH₄ l⁻¹) and with and without ammonium (100 mg N kg⁻¹) pre-incubation. Four months after fertilisation, plots C, G and M did not show significant differences in physicochemical properties and CH₄ oxidising activity. The total number of methanotrophs (determined as the sum the 11 specifically targeted methanotrophs) in the fresh soils was 17.0×10⁶, 13.7×10⁶ and 15.5×10⁶ cells g⁻¹ for treatment C, G and M, respectively. This corresponded to 0.11 to 0.32% of the total bacterial number. The CH₄ oxidising activity increased 10⁵-fold (20–26 mg CH₄ g⁻¹ h⁻¹), the total number of methanotrophs doubled (28–76×10⁶ cells g⁻¹) and the methanotrophic diversity markedly increased in treatments with a pre-incubation at elevated CH₄ concentrations. In all soils and treatments, type II methanotrophs (62–91%) outnumbered type I methanotrophs (9–38%). Methylocystis and Methylosinus species were always most abundant. After pre-incubation with ammonium, CH₄ oxidation was completely inhibited; however, no change in the methanotrophic community structure could be detected.