Emissions of nitrous oxide from a constructed wetland using a groundfilter and macrophytes in waste-water purification of a dairy farm

 In less populated rural areas constructed wetlands with a groundfilter made out of the local soil mixed with peat and planted with common reed (Phragmites australis) are increasingly used to purify waste water. Particularly in the rhizosphere of the reed, nitrification and denitrification processes take place varying locally and temporally, and the question arises to what extent this type of waste-water treatment plant may contribute to the release of N₂O. In situ N₂O measurements were carried out in the two reed beds of the Friedelhausen dairy farm, Hesse, Germany, irrigated with the waste water from a cheese dairy and 70 local inhabitants (12 m³ waste water or 6 kg BOD₅ or 11 kg chemical O₂ demand (COD_Mn) day^–1). During November 1995 to March 1996, the release of N₂O was measured weekly at 1 m distances using eight open chambers and molecular-sieve traps to collect and absorb the emitted N₂O. Simultanously, the N₂O trapped in the soil, the soil temperature, as well as the concentrations of NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, water-soluble C and the pH were determined at depths of 0–20, 20–40 and 40–60 cm. In the waste water from the in- and outflow the concentrations of COD_Mn, BOD₅, NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, as well as the pH, were determined weekly. Highly varying amounts of N₂O were emitted at all measuring dates during the winter. Even at soil temperatures of –1.5  °C in 10 cm depth of soil or 2  °C at a depth of 50 cm, N₂O was released. The highest organic matter and N transformation rates were recorded in the upper 20 cm of soil and in the region closest to the outflow of the constructed wetland. Not until a freezing period of several weeks did the N₂O emissions drop drastically. During the period of decreasing temperatures less NO₃ ^–-N was formed in the soil, but the NH₄ ⁺-N concentrations increased. On average the constructed wetlands of Friedelhausen emitted about 15 mg N₂O-N inhabitant equivalent^–1 day^–1 during the winter period. Nitrification-denitrification processes rather than heterotrophic denitrification are assumed to be responsible for the N₂O production. Received: 28 October 1998     

Nitrification and denitrification in the rhizosphere of rice: the detection of processes by a new multi-channel electrode

 N turnover in flooded rice soils is characterized by a tight coupling between nitrification and denitrification. Nitrification is restricted to the millimetre-thin oxic surface layer while denitrification occurs in the adjacent anoxic soil. However, in planted rice soil O₂ released from the rice roots may also support nitrification within the otherwise anoxic bulk soil. To locate root-associated nitrification and denitrification we constructed a new multi-channel microelectrode that measures NH₄ ⁺, NO₂ ^–, and NO₃ ^– at the same point. Unfertilized, unplanted rice microcosms developed an oxic-anoxic interface with nitrification taking place above and denitrification below ca. 1 mm depth. In unfertilized microcosms with rice plants, NH₄ ⁺, NO₂ ^– and NO₃ ^– could not be detected in the rhizosphere. Assimilation by the rice roots reduced the available N to a level where nitrification and denitrification virtually could not occur. However, a few hours after injecting (NH₄)₂HPO₄ or urea, a high nitrification activity could be detected in the surface layer of planted microcosms and in a depth of 20–30 mm in the rooted soil. O₂ concentrations of up to 150 μM were measured at the same depth, indicating O₂ release from the rice roots. Nitrification occurred at a distance of 0–2 mm from the surface around individual roots, and denitrification occurred at a distance of 1.5–5.0 mm. Addition of urea to the floodwater of planted rice microcosms stimulated nitrification. Transpiration of the rice plants caused percolation of water resulting in a mass flow of NH₄ ⁺ towards the roots, thus supporting nitrification. Received: 23 July 1999     

Influence of N and non-N salts on atmospheric methane oxidation by upland boreal forest and tundra soils

 The short-term (24 h) and medium-term (30 day) influence of N salts (NH₄Cl, NaNO₃ and NaNO₂) and a non-N salt (NaCl) on first-order rate constants, k (h^–1) and thresholds (C_Th) for atmospheric CH₄ oxidation by homogenized composites of upland boreal forest and tundra soils was assessed at salt additions ranging to 20 μmol g^–1 dry weight (dw) soil. Additions of NH₄Cl, NaNO₃ and NaCl to 0.5 μmol g^–1 dw soil did not significantly decrease k relative to watered controls in the short term. Higher concentrations significantly reduced k, with the degree of inhibition increasing with increasing dose. Similar doses of NH₄Cl and NaCl gave comparable decreases in k relative to controls and both soils showed low native concentrations of NH₄ ⁺-N (≤1 μmol g^–1dw soil), suggesting that the reduction in k was due primarily to a salt influence rather than competitive inhibition of CH₄ oxidation by exogenous NH₄ ⁺-N or NH₄ ⁺-N released through cation exchange. The decrease in k was consistently less for NaNO₃ than for NH₄Cl and NaCl at similar doses, pointing to a strong inhibitory effect of the Cl^– counter-anion. Thresholds for CH₄ oxidation were less sensitive to salt addition than k for these three salts, as significant increases in C_Th relative to controls were only observed at concentrations ≥1.0 μmol g^–1 dw soil. Both soils were more sensitive to NaNO₂ than to other salts in the short term, showing a significant decrease in k at an addition of 0.25 μmol NaNO₂ g^–1 dw soil that was clearly attributable to NO₂ ^–. Soils showed no recovery from NaCl, NH₄ ⁺-N or NaNO₃ addition with respect to atmospheric CH₄ oxidation after 30 days. However, soils amended with NaNO₂ to 1.0 μmol NaNO₂ g^–1 dw showed values of k that were not significantly different from controls. Recovery of CH₄-oxidizing ability was due to complete oxidation of NO₂ ^–-N to NO₃ ^–-N. Analysis of soil concentrations of N salts necessary to inhibit atmospheric CH₄ oxidation and regional rates of N deposition suggest that N deposition will not decrease the future sink strength of upland high-latitude soils in the atmospheric CH₄ budget. Received: 30 April 1999     

Recovery of nitrification and production of NO and N2O after exposure of soil to acetylene

Incubation of soil under low partial pressures of acetylene (10 Pa) is a widely used method to specifically inhibit nitrification due to the suicide inhibition of ammonium monooxygenase (AMO), the first enzyme in NH₄ ⁺ oxidation by nitrifying bacteria. Although the inhibition of AMO is irreversible, recovery of activity is possible if new enzyme is synthesized. In experiments with three different soils, NH₄ ⁺ concentrations decreased and NO₃ ^– concentrations increased soon after acetylene was removed from the atmosphere. Recovery of NO production started immediately after the removal of acetylene. The release rates of NO and N₂O were higher in soil samples which were only preincubated with 10 Pa acetylene than in those which were kept in the presence of 10 Pa acetylene. In the permanent presence of 10 Pa acetylene, NH₄ ⁺ and NO₃ ^– concentrations stayed constant, and the release rates of NO and N₂O were low. These low release rates were apparently due to processes other than nitrification. Our experiments showed that the blockage of nitrification by low (10 Pa) acetylene partial pressures is only reliable when the soil is kept in permanent contact with acetylene. Received: 17 July 1996     

Microorganisms in sewage sludge added to an extreme alkaline saline soil affect carbon and nitrogen dynamics

There are plans to vegetate soil of the former lake Texcoco and use wastewater sludge to provide nutrients. However, the Texcoco soil is N depleted, so the amount of N available to the vegetation might be limited and the dynamics of C and N affected. We investigated how emissions of CO₂, N₂O and N₂, and dynamics of mineral N were affected when different types of N fertilizer, i.e. NH₄⁺, NO₃⁻, or unsterilized or sterilized wastewater sludge, were added to the Texcoco soil. An agricultural soil served as control. Sewage sludge added to an alkaline saline soil (Texcoco soil) induced a decrease in concentrations of NH₄⁺ and NO₃⁻. Addition of sewage sludge increased the CO₂ emission rate > two times compared to soil amended with sterilized sludge. The NH₄⁺ concentration was lower when sludge was added to an agricultural soil for the first 28 days and in the Texcoco soil for 56 days compared to soil amended with sterilized sludge. Production of N₂O in the agricultural soil was mainly due to nitrification, even when sludge was added, but denitrification was the main source of N₂O in the Texcoco soil. Microorganisms in the sludge reduced N₂O to N₂, but not the soil microorganisms. It was found that microorganisms added with the sludge accelerated organic material decomposition, increased NH₄⁺ immobilization, and induced immobilization of NO₃⁻ (in Texcoco soil). These results suggest that wastewater sludge improves soil fertility at Otumba (an agricultural soil) and would favour the vegetation of the Texcoco soil (alkaline saline).     

Simulating the dynamics of glucose and NH4+ in alkaline saline soils of the former Lake Texcoco with the Detran model

The turnover of organic matter determines the availability of plant nutrients in unfertilized soils, and this applies particularly to the alkaline saline soil of the former Lake Texcoco in Mexico. We investigated the effects of alkalinity and salinity on dynamics of organic material and inorganic N added to the soil. Glucose labelled with ¹⁴C was added to soil of the former Lake Texcoco drained for different lengths of time, and dynamics of ¹⁴C, C and N were investigated with the Detran model. Soil was sampled from an undrained plot and from three drained for 1, 5 and 8 years, amended with 1000 mg ¹⁴C‐labelled glucose kg^?1 and 200 mg NH₄⁺‐N kg^?1, and incubated aerobically. Production of ¹⁴CO₂ and CO₂, dynamics of NH₄⁺, NO₂^– and NO₃^–, and microbial biomass ¹⁴C, C and N were monitored and simulated with the Detran model. A third stable microbial biomass fraction had to be introduced in the model to simulate the dynamics of glucose, because > 90 mg ¹⁴C kg^?1 soil persisted in the soil microbial biomass after 97 days. The observed priming effect was mostly due to an increased decay of soil organic matter, but an increased turnover of the microbial biomass C contributed somewhat to the phenomenon. The dynamics of NH₄⁺ and NO₃^– in the NH₄⁺‐amended soil could not be simulated unless an immobilization of NH₄⁺ into the microbial biomass occurred in the first day of the incubation without an immediate incorporation of it into microbial organic material. The dynamics of C and a priming effect could be simulated satisfactorily, but the model had to be adjusted to simulate the dynamics of N when NH₄⁺ was added to alkaline saline soils.     

Exchangeable ammonium and nitrate from different nitrogen fertilizer preparations in polyacrylamide-treated and untreated agricultural soils

 High molecular weight, anionic polyacrylamide (PAM) is currently being used as an irrigation water additive to significantly reduce soil erosion associated with furrow irrigation. PAM contains amide-N, and PAM application to soils has been correlated with increased activity of soil enzymes, such as urease and amidase, involved in N cycling. Therefore we investigated potential impacts of PAM treatment on the rate at which fertilizer N is transformed into NH₄ ⁺ and NO₃ ^– in soil. PAM-treated and untreated soil microcosms were amended with a variety of fertilizers, ranging from common rapid-release forms, such as ammonium sulfate [(NH₄)₂SO₄] and urea, to a variety of slow-release formulations, including polymerized urea and polymer-encapsulated urea. Ammonium sulfate was also tested together with the nitrification inhibitor dicyandiamide (DCD). The fertilizers were applied at a concentration of 1.0 mg g^–1, which is comparable to 100 lb acre^–l, or 112 kg ha^–1. Potassium chloride-extractable NH₄ ⁺-N and NO₃ ^–-N were quantified periodically during 2–4 week incubations. PAM treatment had no significant effect on NH₄ ⁺ release rates for any of the fertilizers tested and did not alter the efficacy of DCD as a nitrification inhibitor. However, the nitrification rate of urea and encapsulated urea-derived NH₄ ⁺-N was slightly accelerated in the PAM-treated soil. Received: 16 January 1998     

Influence of soil properties on the turnover of nitric oxide and nitrous oxide by nitrification and denitrification at constant temperature and moisture

 Soils are a major source of atmospheric NO and N₂O. Since the soil properties that regulate the production and consumption of NO and N₂O are still largely unknown, we studied N trace gas turnover by nitrification and denitrification in 20 soils as a function of various soil variables. Since fertilizer treatment, temperature and moisture are already known to affect N trace gas turnover, we avoided the masking effect of these soil variables by conducting the experiments in non-fertilized soils at constant temperature and moisture. In all soils nitrification was the dominant process of NO production, and in 50% of the soils nitrification was also the dominant process of N₂O production. Factor analysis extracted three factors which together explained 71% of the variance and identified three different soil groups. Group I contained acidic soils, which showed only low rates of microbial respiration and low contents of total and inorganic nitrogen. Group II mainly contained acidic forest soils, which showed relatively high respiration rates and high contents of total N and NH₄ ⁺. Group III mainly contained neutral agricultural soils with high potential rates of nitrification. The soils of group I produced the lowest amounts of NO and N₂O. The results of linear multiple regression conducted separately for each soil group explained between 44–100% of the variance. The soil variables that regulated consumption of NO, total production of NO and N₂O, and production of NO and N₂O by either nitrification or denitrification differed among the different soil groups. The soil pH, the contents of NH₄ ⁺, NO₂ ^– and NO₃ ^–, the texture, and the rates of microbial respiration and nitrification were among the important variables. Received: 28 October 1999     

Quantification of nitrogen excretion rates for three lumbricid earthworms using 15N

 Nitrogen excretion rates of ¹⁵N-labeled earthworms and contributions of ¹⁵N excretion products to organic (dissolved organic N) and inorganic (NH₄-N, NO₃-N) soil N pools were determined at 10  °C and 18  °C under laboratory conditions. Juvenile and adult Lumbricus terrestris L., pre-clitellate and adult Aporrectodea tuberculata (Eisen), and adult Lumbricus rubellus (Hoffmeister) were labeled with ¹⁵N by providing earthworms with ¹⁵N-labeled organic substrates for 5–6 weeks. The quantity of ¹⁵N excreted in unlabeled soil was measured after 48 h, and daily N excretion rates were calculated. N excretion rates ranged from 274.4 to 744 μg N g^–1 earthworm fresh weight day^–1, with a daily turnover of 0.3–0.9% of earthworm tissue N. The N excretion rates of juvenile L. terrestris were significantly lower than adult L. terrestris, and there was no difference in the N excretion rates of pre-clitellate and adult A. tuberculata. Extractable N pools, particularly NH₄-N, were greater in soils incubated with earthworms for 48 h than soils incubated without earthworms. Between 13 and 40% of excreted ¹⁵N was found in the ¹⁵N-mineral N (NH₄-N+NO₃-N) pool, and 13–23% was in the ¹⁵N-DON pool. Other fates of excreted ¹⁵N may have been incorporation in microbial biomass, chemical or physical protection in non-extractable N forms, or gaseous N losses. Earthworm excretion rates were combined with earthworm biomass measurements to estimate N flux from earthworm populations through excretion. Annual earthworm excretion was estimated at 41.5 kg N ha^–1 in an inorganically-fertilized corn agroecosystem, and was equivalent to 22% of crop N uptake. Our results suggest that the earthworms could contribute significantly to N cycling in corn agroecosystems through excretion processes. Received: 12 April 1999     

Influence of nitrogen on cellulose and lignin mineralization in blackwater and redwater forested wetland soils

 Microcosms were used to determine the influence of N additions on active bacterial and active fungal biomass, cellulose degradation and lignin degradation at 5, 10 and 15 weeks in soils from blackwater and redwater wetlands in the northern Florida panhandle. Blackwater streams contain a high dissolved organic C concentration which imparts a dark color to the water and contain low concentrations of nutrients. Redwater streams contain high concentrations of suspended clays and inorganic nutrients, such as N and P, compared to blackwater streams. Active bacterial and fungal biomass was determined by direct microscopy; cellulose and lignin degradation were measured radiometrically. The experimental design was a randomized block. Treatments were: soil type (blackwater or redwater forested wetlands) and N additions (soils amended with the equivalent of 0, 200 or 400 kg N ha^–1 as NH₄NO₃). Redwater soils contained higher concentrations of C, total N, P, K, Ca, Mn, Fe, B and Zn than blackwater soils. After N addition and 15 weeks of incubation, the active bacterial biomass in redwater soils was lower than in blackwater soils; the active bacterial biomass in blackwater soils was lower when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. The active fungal biomass in blackwater soils was higher when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. The active fungal biomass in redwater wetland soils was lower when 200 kg N ha^–1, but not when 400 kg N ha^–1, was added. Cellulose and lignin degradation was higher in redwater than in blackwater soils. After 10 and 15 weeks of incubation, the addition of 200 or 400 kg N as NH₄NO₃ ha^–1 decreased cellulose and lignin degradation in both wetland soils to similar levels. This study indicated that the addition of N may slow organic matter degradation and nutrient mineralization, thereby creating deficiencies of other plant-essential nutrients in wetland forest soils. Received: 7 April 1999     

Evaluation of 3,4-dimethylpyrazole phosphate as a nitrification inhibitor in a <Emphasis Type="Italic">Citrus</Emphasis>-cultivated soil

 The objectives of this work were to evaluate the inhibitory action on nitrification of 3,4-dimethylpyrazole phosphate (DMPP) added to ammonium sulphate nitrate [(NH₄)₂SO₄ plus NH₄NO₃; ASN] in a Citrus-cultivated soil, and to study its effect on N uptake. In a greenhouse experiment, 2 g N as ASN either with or without 0.015 g DMPP (1% DMPP relative to NH₄ ⁺-N) was applied 6 times at 20-day intervals to plants grown in 14-l pots filled with soil. Addition of DMPP to ASN resulted in higher levels of NH₄ ⁺-N and lower levels of NO₃ ^–-N in the soil during the whole experimental period. The NO₃ ^–-N concentration in drainage water was lower in the ASN plus DMPP (ASN+DMPP)-treated pots. Also, DMPP supplementation resulted in greater uptake of the fertilizer-N by citrus plants. In another experiment, 100 g N as ASN, either with or without 0.75 g DMPP (1% DMPP relative to NH₄ ⁺-N) was applied to 6-year-old citrus plants grown individually outdoors in containers. Concentrations of NH₄ ⁺-N and NO₃ ^–-N at different soil depths and N distribution in the soil profile after consecutive flood irrigations were monitored. In the ASN-amended soil, nitrification was faster, whereas the addition of the inhibitor led to the maintenance of relatively high levels of NH₄ ⁺-N and NO₃ ^–-N in soil for longer than when ASN was added alone. At the end of the experiment (120 days) 68.5% and 53.1% of the applied N was leached below 0.60 m in the ASN and ASN+DMPP treatments, respectively. Also, leaf N levels were higher in plants fertilized with ASN+DMPP. Collectively, these results indicate that the DMPP nitrification inhibitor improved N fertilizer efficiency and reduced NO₃ ^– leaching losses by retaining the applied N in the ammoniacal form. Received: 31 May 1999     

Effect of climate and soil type on the immobilization of nitrogen by decomposing straw in northern and southern Europe

 Wheat straw enclosed in mesh bags was buried for periods up to 1 year over two seasons in Scottish, Danish and Portuguese soils treated with ¹⁵NH₄NO₃ or NH₄ ¹⁵NO₃. Scottish soils were: Terryvale, a poorly drained sandy loam; and Tipperty, an imperfectly drained brown forest soil with a higher clay content. The Danish soil (Foulum) was a freely drained sandy loam and the Portuguese soils were a sandy soil (Evora) and a clay soil (Beja). During the first month, ¹⁵N was being incorporated into the straw in the Tipperty, Terryvale and Foulum soils simultaneously as the total N content was decreasing. Subsequently, the straws began to show net immobilization and the total N content of the original straw was exceeded in Tipperty and Foulum soils after 4 months and 8 months, respectively. Net immobilization in Terryvale was detected only in the second season and did not occur in the first because of high soil moisture content. The rates of ¹⁵N incorporation were similar in the two Portuguese soils, and a loss of N was only detected after 8 months. After 1 month, in the two clay soils, Beja and Tipperty, ¹⁵NO₃ ^– was incorporated into straw to a greater extent than ¹⁵NH₄ ⁺ and this was attributed to ¹⁵NH₄ ⁺ fixation by clay minerals. In contrast, ¹⁵NH₄ ⁺ was more efficiently incorporated than ¹⁵NO₃ ^– under waterlogged conditions (Terryvale) and NO₃ ^– loss could be attributed to denitrification. The proportion of added ¹⁵N in the straw residue after 1 month varied between 6% and 18% for ¹⁵NH₄ ⁺ and 2% and 23% for ¹⁵NO₃ ^– and immobilization of N in the longer term tended to be greater in soils from northern Europe than from Portugal. Received: 19 January 1998     

Effects of salts and moisture content on N2O emission and nitrogen dynamics in Yellow soil and Andosol in model experiments

 The effects of salt type and its concentration on nitrification, N mineralization and N₂O emission were examined under two levels of moisture content in Yellow soil and Andosol samples as simulated to agriculture under arid/semi-arid conditions and under heavy application of fertilizer in a glass-house, respectively. The salt mixtures were composed of chlorides (NaCl and NH₄Cl) or sulphates [Na₂SO₄ and (NH₄)₂SO₄] and were added at various concentrations (0, 0.1, 0.2, 0.4 and 0.6 M as in the soil solution). These salts were added to non-saline Yellow soil at different moisture contents (45 or 40 and 65% of maximum water-holding capacity; WHC) and their effects on the changes in mineral N (NH₄ ⁺-N and NO₃ ^–-N) concentration as well as N₂O emission were examined periodically during laboratory incubation. We also measured urease activities to know the effect of salts on N mineralization. Furthermore, Ca(NO₃)₂ solution was added at various concentrations (0, 0.1, 0.3, 0.5 and 0.8 M as in the soil solution) to a non-saline Andosol taken from the subsurface layer in a glass-house and incubated at different moisture contents (50% and 70% of WHC) to examine their effects on changes in mineral N. Nitrification was inhibited by high, but remained unaffected by low, salt concentrations. These phenomena were shown in both the model experiments. It was considered that the salinity level for inhibition of nitrification was an electric conductivity (1 : 5) of 1 dS m^–1. This level was independent of the type of salts or soil, and was not affected by soil moisture content. The critical level of salts for urease activities was about 2 dS m^–1. The emission rate of N₂O was maximum at the beginning of the incubation period and stabilized at a low level after an initial peak. There was no significant difference in N₂O emission among the treatments at different salt concentrations, while higher moisture level enhanced N₂O emission remarkably. Received: 29 July 1998     

Nitrogen fertilizers promote denitrification

A laboratory study was conducted to compare the effects of different N fertilizers on emission of N₂ and N₂O during denitrification of NO₃ ^– in waterlogged soil. Field-moist samples of Drummer silty clay loam soil (fine-silty, mixed, mesic Typic Haplaquoll) were incubated under aerobic conditions for 0, 2, 4, 7, 14, 21, or 42 days with or without addition of unlabelled (NH₄)₂SO₄, urea, NH₄H₂PO₄, (NH₄)₂HPO₄, NH₄NO₃ (200 or 1000 mg N kg^–1 soil), or liquid anhydrous NH₃ (1000 mg N kg^–1 soil). The incubated soil samples were then treated with ¹⁵N-labelled KNO₃ (250 mg N kg^–1 soil, 73.7 atom% ¹⁵N), and incubation was carried out under waterlogged conditions for 5 days, followed by collection of atmospheric samples for ¹⁵N analyses to determine labelled N₂ and N₂O. Compared to samples incubated without addition of unlabelled N, all of the fertilizers promoted denitrification of ¹⁵NO₃ ^–. Emission of labelled N₂ and N₂O decreased in the order: Anhydrous NH₃>urea<$>\gg<$> (NH₄)₂HPO₄>(NH₄)₂SO₄≃NH₄NO₃≃NH₄H₂PO₄. The highest emissions observed with anhydrous NH₃ or urea coincided with the presence of NO₂ ^–, and ¹⁵N analyses indicated that these emissions originated from NO₂ ^– rather than NO₃ ^–. Emissions of labelled N₂ and N₂O were significantly correlated with fertilizer effects on soil pH and water-soluble organic C. Received: 17 January 1996     

The short-term cover crops increase soil labile organic carbon in southeastern Australia

Little information is available about the effects of cover crops on soil labile organic carbon (C), especially in Australia. In this study, two cover crop species, i.e., wheat and Saia oat, were broadcast-seeded in May 2009 and then crop biomass was crimp-rolled onto the soil surface at anthesis in October 2009 in southeastern Australia. Soil and crop residue samples were taken in December 2009 to investigate the short-term effects of cover crops on soil pH, moisture, NH₄⁺–N, NO₃⁻–N, soluble organic C and nitrogen (N), total organic C and N, and C mineralization in comparison with a nil-crop control (CK). The soil is a Chromic Luvisol according to the FAO classification with 48.4 ± 2.2% sand, 19.5 ± 2.1% silt, and 32.1 ± 2.1% clay. An exponential model fitting was employed to assess soil potentially labile organic C (C ₀) and easily decomposable organic C for all treatments based on 46-day incubations. The results showed that crop residue biomass significantly decreased over the course of 2-month decomposition. The cover crop treatments had significantly higher soil pH, soluble organic C and N, cumulative CO₂–C, C ₀, and easily decomposable organic C, but significantly lower NO₃⁻–N than the CK. However, no significant differences were found in soil moisture, NH₄⁺–N, and total organic C and N contents among the treatments. Our results indicated that the short-term cover crops increased soil labile organic C pools, which might have implications for local agricultural ecosystem managements in this region.     

Spatial variability of N2O emissions and soil parameters of an arable silt loam – a field study

 The spatial in situ variability of soil N₂O emissions (measured by micro-chambers, radius 0.033 m), N₂O content, water content, NO₃ ^–, NH₄ ⁺, inorganic carbon and organic carbon concentrations was investigated on a silt loam by means of geostatistical methods and nonparametric statistics. The sampling grid consisted of different spacings between sampling points which ranged from 0.1 m to 50 m. There were no significant correlations between N₂O emissions and soil parameters (P>0.1) when all the sampling points were considered. In the centre of the grid a "hot area" was localized with significantly higher N₂O emissions, and NO₃ ^– and NH₄ ⁺ concentrations (P≤0.05). Within this hot area the N₂O soil content significantly correlated with N₂O emissions (P≤0.05). When semiovariograms were computed without data of the hot area samples, N₂O emissions showed a weak spatial correlation (range: 4.3 m). The calculations including all data led to pure nugget effects for all parameters except for soil water content (range >40 m) and N₂O soil content (range 16.4 m). Received: 19 December 1997     

Gross nitrogen mineralization and nitrification rates and their relationships to enzyme activities and the soil microbial biomass in soils treated with dairy shed effluent and ammonium fertilizer at different water potentials

 Gross N mineralization and nitrification rates and their relationships to microbial biomass C and N and enzyme (protease, deaminase and urease) activities were determined in soils treated with dairy shed effluent (DSE) or NH₄ ⁺ fertilizer (NH₄Cl) at a rate equivalent to 200 kg N ha^–1 at three water potentials (0, –10 and –80 kPa) at 20  °C using a closed incubation technique. After 8, 16, 30, 45, 60 and 90 days of incubation, sub-samples of soil were removed to determine gross N mineralization and nitrification rates, enzyme activities, microbial biomass C and N, and NH₄ ⁺ and NO₃ ^– concentrations. The addition of DSE to the soil resulted in significantly higher gross N mineralization rates (7.0–1.7 μg N g^–1 soil day^–1) than in the control (3.8–1.2 μg N g^–1 soil day^–1), particularly during the first 16 days of incubation. This increase in gross mineralization rate occurred because of the presence of readily mineralizable organic substrates with low C : N ratios, and stimulated soil microbial and enzymatic activities by the organic C and nutrients in the DSE. The addition of NH₄Cl did not increase the gross N mineralization rate, probably because of the lack of readily available organic C and/or a possible adverse effect of the high NH₄ ⁺ concentration on microbial activity. However, nitrification rates were highest in the NH₄Cl-treated soil, followed by DSE-treated soil and then the control. Soil microbial biomass, protease, deaminase and urease activities were significantly increased immediately after the addition of DSE and then declined gradually with time. The increased soil microbial biomass was probably due to the increased available C substrate and nutrients stimulating soil microbial growth, and this in turn resulted in higher enzyme activities. NH₄Cl had a minimal impact on the soil microbial biomass and enzyme activities, possibly because of the lack of readily available C substrates. The optimum soil water potential for gross N mineralization and nitrification rates, microbial and enzyme activities was –10 kPa compared with –80 kPa and 0 kPa. Gross N mineralization rates were positively correlated with soil microbial biomass N and protease and urease activities in the DSE-treated soil, but no such correlations were found in the NH₄Cl-treated soil. The enzyme activities were also positively correlated with each other and with soil microbial biomass C and N. The forms of N and the different water potentials had a significant effect on the correlation coefficients. Stepwise regression analysis showed that protease was the variable that most frequently accounted for the variations of gross N mineralization rate when included in the equation, and has the potential to be used as one of the predictors for N mineralization. Received: 10 March 1998     

Carbon and nitrogen dynamics in ageing earthworm casts in grasslands of the eastern plains of Colombia

 The effects of a large species of anecic earthworm, Martiodrilus carimaguensis Jiménez and Moreno, on soil C and N dynamics were investigated in a native savanna and a man-made pasture of the eastern plains of Colombia. We compared, across time (11 months), the total C, total N, NH⁺ ₄ and NO^– ₃ contents in the earthworm casts, the underlying soil and the adjacent soil. Additional sampling of root biomass and macrofauna was performed. In the two management systems, the total C and N contents were higher in casts (4.33–7.50%) than in the bulk soil (2.81–4.08%), showing that the earthworms selected food substrates with high organic contents. In general, C contents significantly increased during cast ageing (+100%), possibly because of CO₂ fixation processes, dead root accumulation and/or macrofaunal activities in casts. In fresh casts, NH⁺ ₄ levels were very high (294.20–233.98 μg g^–1 dry cast) when compared to the soil (26.96–73.95 μg g^–1 dry soil), due to the intense mineralisation processes that occurred during the transit of soil and organic matter through the earthworm gut. During the first week of cast ageing, NH⁺ ₄ levels sharply decreased, while NH^– ₃ levels showed successive peaks in the casts, the underlying soil and the adjacent soil. These results suggested the rapid production of NO^– ₃ by nitrification processes in the fresh casts, followed by diffusion to the nearby soil, first vertically, then horizontally. After 2 weeks of cast ageing, NH⁺ ₄ and NO^– ₃ levels only showed slight variations, likely because of organic matter protection in stable dry casts. The root biomass was higher (1.6–4.7 times) below the old earthworm casts. The ecological significance of these results is discussed. Received: 22 October 1998     

Carbon and nitrogen mineralization dynamics in different soils of the tropics amended with legume residues and contrasting soil moisture contents

Seasonal drought in tropical agroecosystems may affect C and N mineralization of organic residues. To understand this effect, C and N mineralization dynamics in three tropical soils (Af, An₁, and An₂) amended with haricot bean (HB; Phaseolus vulgaris L.) and pigeon pea (PP; Cajanus cajan L.) residues (each at 5 mg g⁻¹ dry soil) at two contrasting soil moisture contents (pF2.5 and pF3.9) were investigated under laboratory incubation for 100–135 days. The legume residues markedly enhanced the net cumulative CO₂–C flux and its rate throughout the incubation period. The cumulative CO₂–C fluxes and their rates were lower at pF3.9 than at pF2.5 with control soils and also relatively lower with HB-treated than PP-treated soil samples. After 100 days of incubation, 32–42% of the amended C of residues was recovered as CO₂–C. In one of the three soils (An₁), the results revealed that the decomposition of the recalcitrant fraction was more inhibited by drought stress than easily degradable fraction, suggesting further studies of moisture stress and litter quality interactions. Significantly (p < 0.05) greater NH₄⁺–N and NO₃⁻–N were produced with PP-treated (C/N ratio, 20.4) than HB-treated (C/N ratio, 40.6) soil samples. Greater net N mineralization or lower immobilization was displayed at pF2.5 than at pF3.9 with all soil samples. Strikingly, N was immobilized equivocally in both NH₄⁺–N and NO₃⁻–N forms, challenging the paradigm that ammonium is the preferred N source for microorganisms. The results strongly exhibited altered C/N stoichiometry due to drought stress substantially affecting the active microbial functional groups, fungi being dominant over bacteria. Interestingly, the results showed that legume residues can be potential fertilizer sources for nutrient-depleted tropical soils. In addition, application of plant residue can help to counter the N loss caused by leaching. It can also synchronize crop N uptake and N release from soil by utilizing microbes as an ephemeral nutrient pool during the early crop growth period.     

Influence of iron pyrites and dicyandiamide on nitrification and ammonia volatilization from urea applied to loess brown earths (luvisols)

Laboratory incubation study showed that iron pyrites retarded nitrification of urea-derived ammonium (NH₄ ⁺), the effect being greatest at the highest level (10000 mg kg^–1 soil). Nitrification inhibition with 10000 mg pyrite kg^–1 soil, at the end of 30 days, was 40.3% compared to 55.9% for dicyandiamide (DCD). The inhibitory effect with lower rates of pyrite (100–500 mg kg^–1) lasted only up to 9 days. Urea+pyrite treatment was also found to have higher exchangeable NH₄ ⁺-N compared to urea alone. DCD-amended soils had the highest NH₄ ⁺-N content throughout. Pyrite-treated soils had about 7–86% lower ammonia volatilization losses than urea alone. Total NH₃ loss was the most with urea+DCD (7.9% of applied N), about 9% more than with urea alone. Received: 11 November 1995