Effect of the herbicide glyphosate on respiration and hydrogen consumption in soil

The effect of glyphosate on soil respiration and Hz oxidation in an agricultural soil was investigated. The effects of the pure herbicide and commercial formulation, Roundup® (Monsanto Company), were compared in soil under both aerobic and anaerobic conditions. Both formulations stimulated O₂ uptake as well as aerobic and anaerobic CO₂ evolution. Roundup caused more stimulation than glyphosate under aerobic incubation conditions; the formulations had an equal effect on anaerobic CO₂ evolution. Hydrogen oxidation was inhibited by both formulations in aerobic and anaerobic soil. Aerobic H₂ oxidation was inhibited to the same extent by both formulations; Roundup had a stronger inhibitory effect on anaerobic H₂ oxidation than did glyphosate.     

Laboratory investigations into the effects of the pesticides mancozeb, chlorothalonil, and prosulfuron on nitrous oxide and nitric oxide production in fertilized soil

Independent soil microcosm experiments were used to investigate the effects of the fungicides mancozeb and chlorothalonil, and the herbicide prosulfuron, on N₂O and NO production by nitrifying and denitrifying bacteria in fertilized soil. Soil cores were amended with NH₄NO₃ or NH₄NO₃ and pesticide, and the N₂O and NO concentrations were monitored periodically for approximately 48 h following amendment. Nitrification is the major source of N₂O and NO in these soils at soil moistures relevant to those observed at the field site where the cores were collected. At pesticide concentrations from 0.02 to 10 times that of a standard single application on a corn crop, N₂O and NO production was inhibited by all three pesticides. Generally N₂O production was inhibited by the pesticides from 10 to 62% and 20 to 98% at the lowest and highest dosages, respectively. Nitric oxide production was generally inhibited from about 5 to 47% and by 20 to 97% at the lowest and highest dosages, respectively. Nitrous oxide and nitric oxide production by nitrification was more susceptible to inhibition by these pesticides than denitrification. Production of both N₂O and NO by nitrification was inhibited by as much as 99%, at the highest concentration of pesticide applied. The net production of N₂O increased as soil moisture increased. The rate of NO production was greatest at the intermediate moistures investigated, between 14 and 19% gravimetric soil moisture, suggestive that nitrification is the dominant source of NO.     

The N2O product ratio of nitrification and its dependence on long-term changes in soil pH

The contribution of nitrification to the emission of nitrous oxide (N₂O) from soils may be large, but its regulation is not well understood. The soil pH appears to play a central role for controlling N₂O emissions from soil, partly by affecting the N₂O product ratios of both denitrification (N₂O/(N₂+N₂O)) and nitrification (N₂O/(NO₂⁻+NO₃⁻). Mechanisms responsible for apparently high N₂O product ratios of nitrification in acid soils are uncertain. We have investigated the pH regulation of the N₂O product ratio of nitrification in a series of experiments with slurries of soils from long-term liming experiments, spanning a pH range from 4.1 to 7.8. ¹⁵N labelled nitrate (NO₃⁻) was added to assess nitrification rates by pool dilution and to distinguish between N₂O from NO₃⁻ reduction and NH₃ oxidation. Sterilized soil slurries were used to determine the rates of chemodenitrification (i.e. the production of nitric oxide (NO) and N₂O from the chemical decomposition of nitrite (NO₂⁻)) as a function of NO₂⁻ concentrations. Additions of NO₂⁻ to aerobic soil slurries (with ¹⁵N labelled NO₃⁻ added) were used to assess its potential for inducing denitrification at aerobic conditions. For soils with pH?5, we found that the N₂O product ratios for nitrification were low (0.2-0.9‰) and comparable to values found in pure cultures of ammonia-oxidizing bacteria. In mineral soils we found only a minor increase in the N₂O product ratio with increasing soil pH, but the effect was so weak that it justifies a constant N₂O product ratio of nitrification for N₂O emission models. For the soils with pH 4.1 and 4.2, the apparent N₂O product ratio of nitrification was 2 orders of magnitude higher than above pH 5 (76‰ and 14‰). This could partly be accounted for by the rates of chemodenitrification of NO₂⁻. We further found convincing evidence for NO₂⁻-induction of aerobic denitrification in acid soils. The study underlines the role of NO₂⁻, both for regulating denitrification and for the apparent nitrifier-derived N₂O emission.     

Acetylene inhibition of nitrous oxide reduction and measurement of denitrification and nitrogen fixation in soil

Reduction of N₂O in moist soil was inhibited completely by 10^?2 atm C₂H₂ and partially by 10^?5 atm C₂H₂. The effect of C₂H₄ was 10⁴ times less than that of C₂H₂. Denitrification of NO^?₃ occurred in anaerobically or aerobically incubated waterlogged soil and in anaerobic but not in aerobic moist soil. In the absence of C₂H₂ there was transient accumulation of N₂O. In the presence of C₂H₂ there was stoichiometric conversion of NO^?₃ to N₂O. Some kinetics of the reduction of N₂O and of NO^?₃ to N₂O are presented. Denitrification of 1 μg added NO^?₃-N.g^? could be measured within 1 h. Stoichiometries of production of N₂O from NO^?₂ and NO^?₃, respectively, and production of CO₂ attributable to denitrification were consistent with reported energy yields. Reduction of C₂H₂ to C₂H₄ occurred immediately following complete denitrification of added NO^?₃. The incubation of soil in the presence and in the absence of C₂H₂ thus permits assay of both denitrification and N₂ fixation and provides information on the mole fraction of N₂O in the products of denitrification.     

Inhibitory effect of nitrate on reduction of N2O to N2 by soil microorganisms

The ability of soils to reduce N₂O to N₂ depends very largely on their NO₃^? content. Low concentrations of NO₃^? delay reduction of N₂O to N₂ by soil microorganisms, and high concentrations of NO₃^? almost completely inhibit this process. The inhibitory effect of NO₃^? on N₂O reduction increases markedly with decrease in soil pH. These observations account for the finding in previous work that accumulation of N₂O during denitrification of NO₃^? in soils incubated in closed systems is favored by high NO₃^? concentration and by low pH. They also indicate that, even if increased N fertilization of soils does not lead to a significant increase in the amount of N volatilized from soils as N₂ and N₂O through denitrification of NO₃^?, it may cause a substantial increase in the ratio of N₂O to N₂ and thereby pose a threat to the stratospheric ozone layer.     

除草剂对不同种植年限柑橘园土壤氮转化过程及温室气体排放的影响

为探讨除草剂施用对柑橘园土壤氮转化及温室气体排放的影响,在实验室培养条件下,研究了0年(林地)、种植10年和30年的柑橘园土壤中分别添加除草剂草甘膦和丁草胺后,尿素态氮含量、硝化和反硝化作用以及温室气体排放的变化。研究结果表明,橘园土壤中尿素第1 d的水解率、氮肥硝化率、反硝化作用损失总量以及N_2O和CO_2排放量显著高于林地土壤(P0.05)。与10年橘园土壤相比,30年橘园土壤显著增加了尿素的水解速率、氮肥硝化率和CO_2排放量(P0.05),但二者的反硝化损失量没有显著差异。施用草甘膦和丁草胺都显著促进了林地土壤的尿素水解(P0.05),第1 d尿素态氮含量分别降低11.20%和12.43%;但对3种土壤氮肥的硝化率均没有明显影响。施用丁草胺显著降低了林地土壤的CO_2排放量(P0.05),对两种橘园土壤的CO_2排放没有明显影响,但明显增加了两种橘园土壤的N_2O排放总量(P0.05),分别比不施除草剂增加56.27%和85.41%;施用草甘膦对3种土壤的N_2O和CO_2排放均没有明显影响。可见,草甘膦和丁草胺的施用不会对柑橘园土壤的氮转化过程产生影响,但丁草胺显著增加了柑橘园土壤的N_2O排放。     

Diversity of denitrifying microflora and ability to reduce N2O in two soils

 The ozone-depleting gas N₂O is an intermediate in denitrification, the biological reduction of NO₃ ^– to the gaseous products N₂O and N₂ gas. The molar ratio of N₂O produced (N₂O/N₂O+N₂) varies temporally and spatially, and in some soils N₂O may be the dominant end product of denitrification. The fraction of NO₃ ^–-N emitted as N₂O may be due at least in part to the abundance and activity of denitrifying bacteria which possess N₂O reductase. In this study, we enumerated NO₃ ^–-reducing and denitrifying bacteria, and compared and contrasted collections of denitrifying bacteria isolated from two agricultural soils, one (Auxonne, soil A) with N₂O as the dominant product of denitrification, the other (Chalons, soil C) with N₂ gas as the dominant product. Isolates were tested for the ability to reduce N₂O, and the presence of the N₂O reductase (nosZ)-like gene was evaluated by polymerase chain reaction (PCR) using specific primers coupled with DNA hybridization using a specific probe. The diversity and phylogenetic relationships of members of the collections were established by PCR/restriction fragment length polymorphism of 16s rDNA. The two soils had similar numbers of bacteria which used NO₃ ^– as a terminal electron acceptor anaerobically. However, the soil A had many more denitrifiers which reduced NO₃ ^– to gaseous products (N₂O or N₂) than did soil C. Collections of 258 and 281 bacteria able to grow anaerobically in the presence of NO₃ ^– were isolated from soil A and soil C, respectively. These two collections contained 66 and 12 denitrifying isolates, respectively, the others reducing NO₃ ^– only as far as NO₂ ^–. The presence of nosZ sequences was generally a poor predictor of N₂O reducing ability: there was agreement between the occurrence of nosZ sequences and the N₂O reducing ability for only 42% of the isolates; 35% of the isolates (found exclusively in soil A) without detectable nosZ sequences reduced N₂O whereas 21% of the isolates carrying nosZ sequences did not reduce this gas under our assay conditions. Twenty-eight different 16S rDNA restriction patterns (using two restriction endonucleases) were distinguished among the 78 denitrifying isolates. Two types of patterns appeared to be common to both soils. Twenty-three and three types of patterns were found exclusively among bacteria isolated from soils A and C, respectively. The specific composition of denitrifying communities appeared to be different between the two soils studied. This may partly explain the differences in the behaviour of the soils concerning N₂O reduction during denitrification. Received: 31 October 1997     

Nitrous oxide emission from frozen grassland soil and during thawing periods

Nitrous oxide (N₂O) was emitted during a frost period from an old grassland as well as during thawing. Soil incubations at various times throughout the freezing period showed that highest emission rates were emitted around 0 °C, and the magnitude of the emission peak increased with the length of the freezing period. Highest N₂O emissions during freezing and thawing were measured from soil previously treated with nitrate (NO₃^‐). The emitted N₂O was produced via reduction of NO₃^‐. The steady drop in N₂O emission at soil temperatures higher than 2 °C coincided with large dinitrogen (N₂) emissions which most likely reflected the increasing enzymatic activity of N₂O reductase with increasing temperatures. Measurements of mineral N concentrations showed that NO₃^‐ and NH₄⁺, which were shortly after fertilizer application immobilized into the microbial biomass, became partly available again through the freezing effect and caused large N₂O emissions in winter. This study provided evidence that N₂O emissions during freezing and thawing in the winter are due to biological rather than chemical activity in soil.     

Temporal in situ dynamics of N<Subscript>2</Subscript>O reductase activity as affected by nitrogen fertilization and implications for the N<Subscript>2</Subscript>O/(N<Subscript>2</Subscript>O + N<Subscript>2</Subscript>) product ratio and N<Subscript>2</Subscript>O mitigation

In vitro, high nitrate (NO₃ ^?) concentrations significantly inhibit N₂O reductase activity. However, little information is available on the in situ temporal effects of excessive N fertilization on soil N₂O reductase activity and the regulation of the N₂O/(N₂ + N₂O) product ratio in agricultural soil. This study examined the monthly in situ dynamics of NO₃ ^? concentration, N₂O reductase activity, and N₂O/(N₂ + N₂O) product ratio for 2 years in loamy soil that had received either continuous N fertilizer at 400 kg N ha^?1 year^?1 for 15 years (N400) or no N fertilizers (CK). N₂O reductase activity was significantly lower under the N400 treatment than under the CK and correlated negatively with soil NO₃ ^? concentration. The decrease in N₂O reductase activity resulted in the N₂O/(N₂ + N₂O) product ratio increasing. These results demonstrate that excessive N fertilization has the potential to increase N₂O emissions by reducing N₂O reductase activity in soils. These results highlight the need for N₂O mitigation options to embrace the reduction of soil NO₃ ^? concentrations.     

高氮和NO2-对中亚热带森林土壤N2O和NO产生的影响

利用15N同位素标记方法,研究在两种水分条件即60％和90％ WHC下,添加硝酸盐(NH4NO3,N 300 mg kg-1)和亚硝酸盐(NaNO2,N 1 mg kg-1)对中亚热带天然森林土壤N2O和NO产生过程及途径的影响.结果表明,在含水量为60％ WHC的情况下,高氮输入显著抑制了N2O和NO的产生(p＜0.01);但当含水量增为90％ WHC后,实验9h内抑制N2O产生,之后转为促进.所有未灭菌处理在添加NO2-后高氮抑制均立即解除并大量产生N2O和NO,与对照成显著差异(p＜0.01),在60％ WHC条件下,这种情况维持时间较短(21 h),但如果含水量高(90％ WHC)这种情况会持续很长时间(2周以上),说明水分有效性的提高和外源NO2-在高氮抑制解除中起到重要作用.本实验中N2O主要来源于土壤反硝化过程,而且加入未标记NO2-后导致杂合的N2O(14N15NO)分子在实验21 h内迅速增加,表明这种森林土壤的反硝化过程可能主要是通过真菌的“共脱氮”来实现,其贡献率可多达80％以上.Spearman秩相关分析表明未灭菌土壤NO的产生速率与N2O产生速率成显著正相关性(p＜0.05),土壤含水量越低二者相关性越高.灭菌土壤添加NO2-能较未灭菌土壤产生更多的NO,但却几乎不产生N2O,表明酸性土壤的化学反硝化对NO的贡献要大于N2O.     

Glyphosate- and imazethapyr-induced effects on yield, nodule mass and biological nitrogen fixation in field-grown glyphosate-resistant soybean

Over half of the 21 Mha of soybean planted in Brazil is now transgenic glyphosate-resistant (GM_RR). A field experiment was carried out to investigate whether the application of glyphosate or imazethapyr to the GM_RR variety reduced the input of N₂ fixation (BNF). No effects on yield, total N accumulation, nodulation and BNF (δ¹⁵N) could be assigned to the genetic modification of the plant. Imazethapyr reduced soybean yield but had no significant effect on BNF. Even though yields were not affected by glyphosate, the significant reduction of nodule mass and BNF to the GM_RR suggests that the use of this herbicide could lead to an increased dependence on soil N and consequently an eventual decrease of SOM reserves.     

Nitrification and Methane Oxidation in Forest Soil: Acid Deposition, Nitrogen Input and Plant Effects

In a laboratory incubation experiment, nitrification potential, methane oxidation, N₂O and CO₂ release were studied in the organic soil layer (0–10 cm) of field lysimeters containing re-established soil profiles from a 100-year-old Scots pine (Pinus sylvestris) forest of Norway. The experiment was designed as a full factorial (3 factors; N fertilisation rates, soil acidification, and plants), with three replicates. The more acidic irrigation (pH 3) significantly reduced nitrification potential and N₂O fluxes, methane oxidation and CO₂ release. We concluded that the reduction in soil N₂O release by severe acid deposition is partly due to reduction in nitrification potential. The highest N₂O fluxes were observed in the combination of fertilised planted and less acidic pH treatment. N fertilisation (90 kg N ha^?1 y^?1 with NH₄NO₃) increased soil N₂O release by a factor of 8 and decreased CH₄ oxidation by 60–80%. Plant effects on soil nitrification potential and methane oxidation rates are discussed.     

Short-term effects of ammonium nitrogen in upland pasture soil affected or not affected by cattle

The short-term effects of excessive NH₄⁺-N on selected characteristics of soil unaffected (low annual N inputs) and affected (high annual N inputs) by cattle were investigated under laboratory conditions. The major hypothesis tested was that above a theoretical upper limit of NH₄⁺ concentration, an excess of NH₄⁺-N does not further increase NO₃⁻ formation rate in the soil, but only supports accumulation of NO₂⁻-N and gaseous losses of N as N₂O. Soils were amended with 10 to 500 μg NH₄⁺-N g⁻¹ soil. In both soils, addition of NH₄⁺-N increased production of NO₃⁻-N until some limit. This limit was higher in cattle-affected soil than in unaffected soil. Production of N₂O increased in the whole range of amendments in both soils. At the highest level of NH₄⁺-N addition, NO₂⁻-N accumulated in cattle-affected soil while NO₃⁻-N production decreased in cattle-unaffected soil. Despite being statistically significant, observed effects of high NH₄⁺-N addition were relatively weak. Uptake of mineral N, stimulated by glucose amendment, decreased the mineral N content in both soils, but it also greatly increased production of N₂O.     

DENITRIFICATION IN A VERY ACID TROPICAL SOIL

In a very acid upland clay surface soil and with glucose added to give initial C/N weight ratios (added glucose-C: NO₃-N) in the soil of 0, 2 and 5, the rates of evolution of N₂ and N₂O were maximum at C/N = 2 but were significantly less at 0 and 5. The total N₂ and N₂O production was highest at C/N = 0, confirming that increasing amounts of glucose immobilised more nitrate into the biomass. As with added NO^?₃-N, the time lag, preceding a maximum ‘steady state’ rate of N₂0 evolution, increased regularly with increasing glucose. Within this ‘steady state’ period, the gaseous CO₂-C/(N₂+ N₂O)-N weight ratio in the effluent gas are between 1.0 and 1.3, which corresponds well with the stoichiometric ratios of 1.07 and 1.29 for the reduction of NO^?₃ to N₂O and N₂ respectively. Before and after this period, this gaseous C/N ratio was much higher. Denitrification was not observed in subsurface soil even after adding 100 mg kg^?1glucose-C although it contained 4 times as much indigenous nitrate as the surface soil. Inoculating this soil with increasing amounts of the surface soil, up to 15 per cent by weight, induced substantial increases in the rates and amounts of denitrification. The effects of increasing the soil pH. of introducing increasing oxygen concentrations in the influent gas. and the fate of added NH⁺₄-N, are briefly reported here. In these experiments. NO^?₂-N did not accumulate in the incubated soil nor was there any NH₃in the effluent gas. Evolution of N₂ only occurred when N₂O evolution was in its final stages.     

Nitrous oxide emission as affected by changes in soil water content and nitrogen fertilization

Nitrous oxide emission was measured in laboratory incubations of an alluvial soil (58% clay, pH 7.4). The soil was amended with 40 mg N kg⁻¹ as NaNO₃ or NH₄Cl, or with NaCl as a control. Each fertilization treatment was adjusted to three different water contents: constant 60% WHC (water-holding capacity), constant 120% WHC, and water content alternating between 60 and 120% WHC. During an 8-day incubation period N₂O emission rates and inorganic nitrogen concentrations in soil (NH₄⁺, NO₂⁻, NO₃⁻) were determined at regular intervals. In the control and after nitrate application small N₂O emission rates occurred with only minor variations over time, and no differences between the water treatments. In contrast, with ammonium application N₂O emission rates were much higher during the first two days of incubation, with peaks in the constant 60% WHC and 120% WHC at day 1 and in the changing-water treatment at day 2, when the first wet period (120% WHC) was completed. This N₂O peak in the changing-water treatment was 4 to 9 times higher than with constant WHC and occurred when both, NH₄⁺ and NO₂⁻ concentrations declined sharply. Thus, this N₂O emission flush can be attributed to nitrifier denitrification. After the second rewetting of the NH₄⁺-amended soil no further N₂O emission peak was observed, being in accordance with small NH₄⁺ and NO₂⁻ concentrations in soil at that time. The unexpectedly small N₂O fluxes in the constant 120% WHC treatment after nitrate application were probably caused by the reduction of N₂O to N₂ under the prevailing conditions. It can be concluded that continuous wetting or flooding of a soil is an effective measure to reduce N₂O emissions immediately after the application of NH₄⁺ fertilizers.     

Effects of glyphosate on rhizosphere soil microbial communities under two different plant compositions by cultivation-dependent and -independent methodologies

We studied, under two different plant compositions, the short-term effects of glyphosate on rhizosphere soil microbial communities through the utilization of cultivation-dependent and -independent techniques. A short-term pot study was carried out using factorial treatments that included two different compositions of forage plant species (triticale versus a mixture of triticale and pea) and two concentrations of glyphosate (50 and 500 mg active ingredient kg⁻¹ soil, as a commercial formulation, Roundup Plus) arranged in a completely randomized design experiment with four replicates. Control plants (no glyphosate added) were clipped in an attempt to compare two methods of weed control (manual = clipping; chemical = herbicide treatment). Rhizosphere soil was sampled 15 and 30 days after glyphosate treatment and the following soil components were determined: potentially mineralizable nitrogen, ammonium content, community-level physiological profiles using Biolog Ecoplates™, DNA microbial biomass and genotype diversity by means of PCR-DGGE. Fifteen days after herbicide treatment, a glyphosate-induced stimulation of the activity and functional diversity of the cultivable portion of the heterotrophic soil microbial community was observed, most likely due to glyphosate acting as an available source of C, N and P. On the other hand, 30 days after herbicide treatment, both the activity and diversity of the rhizosphere soil microbial communities showed an inconsistent response to glyphosate addition. Apart from its intended effect on plants, glyphosate had non-target effects on the rhizosphere soil microbial community which were, interestingly, more enhanced in triticale than in “triticale + pea” pots. Biolog™ was more sensitive than PCR-DGGE to detect changes in soil microbial communities induced by glyphosate and plant composition.     

Nitrous oxide dynamics during denitrification along a hydrological gradient of subtropical grasslands

Nitrous oxide (N₂O) dynamics during denitrification, including N₂O production and reduction, particularly as related to soil depth, are poorly understood. The objective of this study was to investigate the rates of N₂O production and reduction processes at various soil depths along a hydrological gradient in grazed subtropical grasslands. A batch incubation study was conducted on soils collected along a hydrological gradient representing isolated wetland (Center), transient edge (Edge) and pasture upland (Upland) in south-central Florida. Significantly different N₂O production and reduction rates between hydrological zones were observed for surface soils (0–10 cm) under ambient conditions, with average N₂O production rates of 0.368, 0.178 and 0.003 N₂O-N kg⁻¹ dry soil h⁻¹ for Center, Edge and Upland, respectively, and average N₂O reduction rates of 0.063, 0.132 and 0.002 N₂O-N kg⁻¹ dry soil h⁻¹. Nitrous oxide production and reduction in subsurface soils maintained low rates and showed small variations between depths and hydrological zones. Our results suggest that N₂O dynamics were affected by depth, mainly through labile organic carbon (C) and microbial biomass C, being influenced by hydrological zone primarily through soil NO₃^- content. The spatial distribution of N₂O fluxes from denitrification along the hydrological gradient is likely attributed to the differences in N₂O production and reduction in surface soils.     

Zinc toxicity on N2O reduction declines with time in laboratory spiked soils and is undetectable in field contaminated soils

Denitrification assays in soils spiked with zinc salt have shown inhibition of the N₂O reduction resulting in increased soil N₂O fluxes with increasing soil Zn concentration. It is unclear if the same is true for environmentally contaminated soils. Net production of N₂O and N₂ was monitored during anaerobic incubations (25 °C, He atmosphere) of soils freshly spiked with ZnCl₂ and of corresponding soils that were gradually enriched with metals (mainly Zn) in the field by previous sludge amendments or by corrosion of galvanized structures. Total denitrification activity (i.e. the sum of N₂O+N₂ production rate) was not inhibited by freshly added Zn salts up to 1600 mg Zn kg⁻¹, whereas N₂O reduction decreased by 50% (EC₅₀) at total Zn concentrations of 231 mg Zn kg⁻¹ (ZEV soil) and 368 mg Zn kg⁻¹ (TM soil). In contrast, N₂O reduction was not reduced by soil Zn in any of the field contaminated soils, even at total soil Zn or soil solution Zn concentrations exceeding more than 5 times corresponding EC₅₀'s of the freshly spiked soil. The absence of adverse effects in the field contaminated soils was unrelated to soil NO₃ or organic matter concentration. Ageing (2-8 weeks) and soil leaching after spiking reduced the toxicity of Zn on N₂O reduction, either expressed as total Zn or soil solution Zn, suggesting adaptation reactions. However, no full recovery after spiking was identified at the largest incubation period in one soil. In addition, the denitrification assay performed with sewage sludge showed elevated N₂O release in Zn contaminated sludges (>6000 mg Zn kg⁻¹ dry matter) whereas this was not observed in low Zn sludge (<1000 mg Zn kg⁻¹ dry matter) suggesting limits to adaptation reactions in the sludge particles. It is concluded that the use of soils spiked with Zn salts overestimates effects on N₂O reduction. Field data on N₂O fluxes in sludge amended soils are required to identify if metals indeed promote N₂O emissions in sludge amended soils.     

Emission of nitrous oxide and carbon dioxide and dynamics of mineral N in wastewater sludge,vermicompost or inorganic fertilizer amended soil at different water contents: A laboratory study

Liming or vermicomposting eliminates pathogens from wastewater sludge, but might affect CO₂ and N₂O emissions when added to soil. Soil incubated at 40%, 60%, 80% and 100% of its water holding capacity (WHC) was amended with limed or unlimed wastewater sludge, vermicompost or inorganic fertilizer, while emissions of N₂O and CO₂ and mineral N concentrations were monitored in aerobic incubation experiment for 7 days. Application of unlimed wastewater sludge significantly increased the emission of CO₂ compared to the unamended soil, but not the other treatments except when unlimed wastewater sludge was added to soil incubated at 60% WHC. The emission of CO₂, was generally largest in soil incubated at 60% WHC and lowest in soil incubated at 100% WHC. The emission of N₂O after 1 day was significantly larger in soil amended with unlimed wastewater sludge compared to the other treatments, but not when soil was incubated at 100% WHC. The emission of N₂O increased with increased soil water content. The concentration of NH₄⁺ was largest in soil amended with limed or unlimed wastewater sludge and lowest in the unamended soil and soil water content had no clear effect on it. In soil incubated at 40%, 60% and 80% WHC, the largest amount of NO₃⁻ was found in soil amended with inorganic fertilizer and vermicompost and the lowest in the soil amended with unlimed wastewater sludge. The concentration of NO₃⁻ in soil decreased when the soil water content increased in all treatments, except in the soil amended with unlimed wastewater sludge. It was found that water content affected the emission of CO₂ of N₂O and the concentration of NO₃⁻, but not the amount of NH₄⁺ and NO₂⁻ in soil. Application of unlimed wastewater sludge increased the emissions of CO₂ and N₂O and the concentrations of NH₄⁺, but decreased the amount of NO₃⁻ in soil.     

Aeration effects on CO2, N2O,and CH4 emission and leachate composition of a forest soil

The availability of O₂ is one of the most important factors controlling the chemical and biological reactions in soils. In this study, the effects of different aeration conditions on the dynamics of the emission of trace gases (CO₂, N₂O, CH₄) and the leachate composition (NO₃^‐, DOC, Mn, Fe) were determined. The experiment was conducted with naturally structured soil columns (silty clay, Vertisol) from a well aerated forest site. The soil monoliths were incubated in a microcosm system at different O₂ concentrations (0, 0.001, 0.005, 0.01, 0.05, and 0.205 m³ m^‐3 in the air flow through the headspace of the microcosms) for 85 days. Reduced O₂ availability resulted in a decreased CO₂ release but in increased N₂O emission rates. The greatest cumulative N₂O emissions (= 1.6 g N₂O‐N m^‐2) were observed at intermediate O₂ concentrations (0.005 and 0.01 m³ m^‐3) when both nitrification and denitrification occurred simultaneously in the soil. Cumulative N₂O emissions were smallest (= 0.05 g N₂O‐N m^‐2) for the aeration with ambient air (O₂ concentration: 0.205 m³ m^‐3), although nitrate availability was greatest in this treatment. The emission of CH₄ and leaching of Mn and Fe were restricted to the soil columns incubated under completely anoxic conditions. The sequence of the reduction processes under completely anoxic conditions complied with the thermodynamic theory: soil nitrate was reduced first, followed by the reduction of Mn(IV) and Fe(III) and finally CO₂ was reduced to CH₄. The re‐aeration of the soil columns after 85 days of anoxic incubation terminated the production of CH₄ and dissolved Fe and Mn in the soil but strongly increased the emission rates of CO₂ and N₂O and the leaching of NO₃^‐ probably because of the accumulation of DOC and NH₄⁺ during the previous anoxic period.