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     

Effects of 4-amino 1,2,4-triazole, dicyandiamide and encapsulated calcium carbide on nitrification inhibition in a subtropical soil under upland and flooded conditions

 Nitrification inhibition of soil and applied fertilizer N is desirable as the accumulation of nitrates in soils in excess of plant needs leads to enhanced N losses and reduced fertilizer N-use efficiency. In a growth chamber experiment, we studied the effects of two commercial nitrification inhibitors (NIs), 4-amino 1,2,4-triazole (ATC) and dicyandiamide (DCD), and a commonly available and economical material, encapsulated calcium carbide (CaC₂) (ECC) on the nitrification of soil and applied NH₄ ⁺-N in a semiarid subtropical Tolewal sandy loam soil under upland [60% water-filled pore space (WFPS)] and flooded conditions (120% WFPS). Nitrification of the applied 100 mg NH₄ ⁺-N kg^–1 soil under upland conditions was retarded most effectively (93%) by ECC for up to 10 days of incubation, whereas for longer periods, ATC was more effective. After 20 days, only 16% of applied NH₄ ⁺-N was nitrified with ATC as compared to 37% with DCD and 98% with ECC. Under flooded soil conditions, nitrates resulting from nitrification quickly disappeared due to denitrification, resulting in a tremendous loss of fertilizer N (up to 70% of N applied without a NI). Based on four indicators of inhibitor effectiveness, namely, concentration of NH₄ ⁺-N and NO₃ ^–-N, percent nitrification inhibition, ratio of NH₄ ⁺-N/NO₃ ^–-N, and total mineral N, ECC showed the highest relative efficiency throughout the 20-day incubation under flooded soil conditions. At the end of the 20-day incubation, 96%, 58% and 38% of applied NH₄ ⁺-N was still present in the soil where ECC, ATC and DCD were used, respectively. Consequently, nitrification inhibition of applied fertilizer N in both arable crops and flooded rice systems could tremendously minimize N losses and help enhance fertilizer N-use efficiency. These results suggest that for reducing the nitrification rate and resultant N losses in flooded soil systems (e.g. rice lowlands), ECC is more effective than costly commercial NIs. Received: 25 May 2000     

Influence of green manuring with Sesbania rostrata and Aeschynomene afraspera or urea on dynamics and uptake of nutrients by wetland rice

Nutrient concentrations in the soil and crop uptake from incorporated green manure and urea in flooded rice was studied in field experiments. Release of plant-available nitrogen (NH₄ ⁺-N) from green manure was slightly delayed compared with that from prilled urea (PU) because Sesbania rostrata L. and Aeschynomene afraspera L. released the N gradually after their decomposition, whereas N became available immediately after PU application. Exchangeable NH₄ ⁺-N concentration in soil peaked at 163 mg kg^–1 in the transplanted rice (TPR) and 198 mg kg^—1 in broadcast-seeded rice (BSR) at 0 and 1 week after PU application. Broadcast-seeded rice depleted NH₄ ⁺-N faster than did TPR because of the crop‘s vigorous growth in the former during the early stage. Soil solution NH₄ ⁺-N followed a similar trend to that of soil NH₄ ⁺-N. Incorporation of S. rostrata and A. afraspera increased the concentration of P, K⁺, Fe²⁺ and Mn²⁺ in soil solution more than did the application of PU. However, zinc concentration decreased in all treatments. Both PU and green manure increased the N status of the rice plants and enhanced the uptake of P, K, Fe, Mn and Zn by the rice crop. This suggests that application of green manures improves the uptake of these nutrients by the crop. The highest apparent N recovery was obtained with PU followed by green manure. Received: 11 November 1996     

Evaluation of biological and chemical nitrogen indices for predicting nitrogen-supplying capacity of paddy soils in the Taihu Lake region,China

Simple and rapid chemical indices of soil nitrogen (N)-supplying capacity are necessary for fertilizer recommendations. In this study, pot experiment involving rice, anaerobic incubation, and chemical analysis were conducted for paddy soils collected from nine locations in the Taihu Lake region of China. The paddy soils showed large variability in N-supplying capacity as indicated by the total N uptake (TNU) by rice plants in a pot experiment, which ranged from 639.7 to 1,046.2 mg N pot⁻¹ at maturity stage, representing 5.8% of the total soil N on average. Anaerobic incubation for 3, 14, 28, and 112 days all resulted in a significant (P < 0.01) correlation between cumulative mineral NH₄⁺-N and TNU, but generally better correlations were obtained with increasing incubation time. Soil organic C, total soil N, microbial C, and ultraviolet absorbance of NaHCO₃ extract at 205 and 260 nm revealed no clear relationship with TNU or cumulative mineral NH₄⁺-N. Soil C/N ratio, acid KMnO₄-NH₄⁺-N, alkaline KMnO₄-NH₄⁺-N, phosphate–borate buffer extractable NH₄⁺-N (PB-NH₄⁺-N), phosphate–borate buffer hydrolyzable NH₄⁺-N (PB_HYDR-NH₄⁺-N) and hot KCl extractable NH₄⁺-N (H_KCl−NH₄⁺-N) were all significantly (P < 0.05) related to TNU and cumulative mineral NH₄⁺-N of long-term incubation (>28 days). However, the best chemical index of soil N-supplying capacity was the soil C/N ratio, which showed the highest correlation with TNU at maturity stage (R = −0.929, P < 0.001) and cumulative mineral NH₄⁺-N (R = −0.971, P < 0.001). Acid KMnO₄-NH₄⁺-N plus native soil NH₄⁺-N produced similar, but slightly worse predictions of soil N-supplying capacity than the soil C/N ratio.     

Nitrogen mineralization and CO2 and N2O emissions in a sandy soil amended with original or acidified pig slurries or with the relative fractions

The following six pig slurries obtained after acidification and/or solid/liquid separation were used in the research: original (S) and acidified (AS) pig slurry, nonacidified (LF) and acidified (ALF) pig slurry liquid fraction, and nonacidified (SF) and acidified (ASF) pig slurry solid fraction. Laboratory incubations were performed to assess the effect of the application of these slurries on N mineralization and CO₂ and N₂O emissions from a sandy soil. Acidification maintained higher NH₄ ⁺-N contents in soil particularly in the ALF-treated soil where NH₄ ⁺-N contents were two times higher than in LF-treated soil during the 55–171-day interval. At the end of the incubation (171 days), 32.9 and 24.2 mg N kg⁻¹ dry soil were mineralized in the ASF- and SF-treated soils, respectively, but no mineralization occurred in LF- and S-treated soils, although acidification decreased N immobilization in ALF- (−25.3 mg N kg⁻¹ soil) and AS- (−12.7 mg N kg⁻¹ soil) compared to LF- (−34.4 mg N kg⁻¹ soil) and S-treated (−18.6 mg N kg⁻¹ soil) soils, respectively. Most of the dissolved CO₂ was lost during the acidification process. More than 90% of the applied C in the LF-treated soil was lost during the incubation, indicating a high availability of the added organic compounds. Nitrous oxide emissions occurred only after day 12 and at a lower rate in soils treated with acidified than nonacidified slurries. However, during the first 61 days of incubation, 1,157 μg N kg⁻¹ soil was lost as N₂O in the AS-treated soil and only 937 in the S-treated soil.     

Fixation and defixation of ammonium in soils: a review

Fixed NH₄⁺ (NH₄⁺ _f) and fixation and defixation of NH₄⁺ in soils have been the subject of a number of investigations with conflicting results. The results vary because of differences in methodology, soil type, mineralogical composition, and agro-climatic conditions. Most investigators have determined NH₄⁺ _f using strong oxidizing agents (KOBr or KOH) to remove organic N and the remaining NH₄⁺ _f does not necessarily reflect the fraction that is truly available to plants. The content of native NH₄⁺ _f in different soils is related to parent material, texture, clay content, clay mineral composition, potassium status of the soil and K saturation of the interlayers of 2:1 clay minerals, and moisture conditions. Evaluation of the literature shows that the NH₄⁺ _f-N content amounts to 10–90 mg kg⁻¹ in coarse-textured soils (e.g., diluvial sand, red sandstone, granite), 60–270 mg kg⁻¹ in medium-textured soils (loess, marsh, alluvial sediment, basalt) and 90–460 mg kg⁻¹ in fine-textured soils (limestone, clay stone). Variable results on plant availability of NH₄⁺ _f are mainly due to the fact that some investigators distinguished between native and recently fixed NH₄⁺ while others did not. Recently fixed NH₄⁺ is available to plants to a greater degree than the native NH₄⁺ _f, and soil microflora play an important role in the defixation process. The temporal changes in the content of recently fixed NH₄⁺ suggest that it is actively involved in N dynamics during a crop growth season. The amounts of NH₄⁺ defixed during a growing season varied greatly within the groups of silty (20–200 kg NH₄⁺-N ha⁻¹ 30 cm⁻¹) as well as clayey (40–188 kg NH₄⁺-N ha⁻¹ 30 cm⁻¹) soils. The pool of recently fixed NH₄⁺ may therefore be considered in fertilizer management programs for increasing N use efficiency and reducing N losses from soils.     

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     

Crop residues and fertilizer nitrogen influence residue decomposition and nitrous oxide emission from a Vertisol

Crop residues with high C/N ratio immobilize N released during decomposition in soil, thus reducing N losses through leaching, denitrification, and nitrous oxide (N₂O) emission. A laboratory incubation experiment was conducted for 84 days under controlled conditions (24°C and moisture content 55% of water-holding capacity) to study the influence of sugarcane, maize, sorghum, cotton and lucerne residues, and mineral N addition, on N mineralization–immobilization and N₂O emission. Residues were added at the rate of 3 t C ha⁻¹ to soil with, and without, 150 kg urea N ha⁻¹. The addition of sugarcane, maize, and sorghum residues without N fertilizer resulted in a significant immobilization of soil N. Amended soil had significantly (P < 0.05) lower NO₃⁻–N, which reached minimum values of 2.8 mg N kg⁻¹ for sugarcane (at day 28), 10.3 mg N kg⁻¹ for maize (day 7), and 5.9 mg N kg⁻¹ for sorghum (day 7), compared to 22.7 mg N kg⁻¹ for the unamended soil (day 7). During 84 days of incubation, the total mineral N in the residues + N treatments were decreased by 45 mg N kg⁻¹ in sugarcane, 34 mg kg⁻¹ in maize, 29 mg kg⁻¹ in sorghum, and 16 mg kg⁻¹ in cotton amended soil compared to soil + N fertilizer, although soil NO₃⁻–N increased by 7 mg kg⁻¹ in lucerne amended soil. The addition of residues also significantly increased amended soil microbial biomass C and N. Maximum emissions of N₂O from crop residue amended soils occurred in the first 4–5 days of incubation. Overall, after 84 days of incubation, the cumulative N₂O emission was 25% lower with cotton + N fertilizer, compared to soil + N fertilizer. The cumulative N₂O emission was significantly and positively correlated with NO₃⁻–N (r = 0.92, P < 0.01) and total mineral N (r = 0.93, P < 0.01) after 84 days of incubation, and had a weak but significant positive correlation with cumulative CO₂ in the first 3 and 5 days of incubation (r = 0.59, P < 0.05).     

Nitrogen uptake and growth of two citrus rootstock seedlings in a sandy soil receiving different controlled-release fertilizer sources

Understanding the fate of different forms of nitrogen (N) fertilizers applied to soils is an important step in enhancing N use efficiency and minimizing N losses. The growth and N uptake of two citrus rootstocks, Swingle citrumelo (SC), and Cleopatra mandarin (CM), seedlings were evaluated in a pot experiment using a Candler fine sand (hyperthermic, uncoated, Typic Quartzipsamments) without N application or with 400 mg N kg^–1 applied as urea or controlled-release fertilizers (CRF; either as Meister, Osmocote, or Poly-S). Meister and Osmocote are polyolefin resin-coated urea with longevity of N release for 270 days (at 25°C). Poly-S is a polymer and sulfur-coated urea with release duration considerably shorter than that of either Meister or Osmocote. The concentrations of 2 M KCl extractable nitrate nitrogen (NO₃ ^–-N) and ammonium nitrogen (NH₄ ⁺-N) in the soil sampled 180 days and 300 days after planting were greater in the soil with SC than with CM rootstock seedlings. In most cases, the extractable NH₄ ⁺ and NO₃ ^– concentrations were greater for the Osmocote treatment compared to the other N sources. For the SC rootstock seedlings, dry weight was greater with Meister or Poly-S compared with either Osmocote or urea. At the end of the experiment, ranking of the various N sources, with respect to total N uptake by the seedlings, was: Meister = Osmocote > Poly-S > Urea > no N for CM rootstock, and Meister = Poly-S = Osmocote > Urea > no N for SC rootstock. The study demonstrated that for a given rate of N application the total N uptake by seedlings was greater for the CRF compared to urea treatment. This suggests that various N losses were lower from the CRF source as compared to those from soluble fertilizers. Received: 11 April 1997     

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     

Nitrous oxide emission from different fertilizers and its mitigation by nitrification inhibitors in irrigated rice

 N₂O emissions from a transplanted irrigated rice grown on a Typic Ustochrept soil at New Delhi, India, were studied to evaluate the effect of N fertilizers, i.e. urea and (NH₄)₂SO₄, alone and in combination with the nitrification inhibitors dicyandiamide (DCD) and thiosulphate. The addition of urea and (NH₄)₂SO₄ increased N₂O emissions considerably when compared to no fertilizer N application (control). N₂O measurement in the field was done by a closed-chamber method for a period of 98 days. The application of urea with DCD and thiosulphate reduced N₂O fluxes considerably. The highest total N₂O-N emission (235 g N₂O-N ha^–1) was from the (NH₄)₂SO₄ treatment, which was significantly higher than the total N₂O-N emission from the urea treatment (160 g N₂O-N ha^–1). DCD reduced N₂O-N emissions by 11% and 26% when applied with urea and(NH₄)₂SO₄, respectively, whereas thiosulphate in combination with urea reduced N₂O-N emissions by 9%. Total N₂O-N emissions were found to range from 0.08% to 0.14% of applied N. N₂O emissions were low during submergence and increased substantially during drainage of standing water. Received: 20 October 1999     

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     

Methane oxidation in arable soil as inhibited by ammonium, nitrite, and organic manure with respect to soil pH

 The effects of inorganic N and organic manure, applied to a loamy arable soil, on CH₄ oxidation were investigated in laboratory incubation experiments. Applications (40 mg N kg^–1) of NH₄Cl, (NH₄)₂SO₄, and urea caused strong instantaneous inhibition of CH₄ oxidation by 96%, 80%, and 84%, respectively. After nitrification of the added N the inhibitory effect was not fully reversible, resulting in an residual inhibition of 21%, 16%, and 25% in the NH₄Cl, (NH₄)₂SO₄, and urea treatments, respectively. With large NH₄ ⁺ applications [240 mg N kg^–1 as (NH₄)₂SO₄] the residual inhibition was as high as 64%. Exogenous NO₂ ^– (40 mg NO₂ ^–-N kg^–1) initially inhibited CH₄ oxidation by 84%, decreasing to 41% after its oxidation. Therefore, applied NO₂ ^– was a more effective inhibitor of CH₄ consumption than NH₄ ⁺. Temporary accumulation of NO₂ ^– during nitrification of added N was small (maximum: 1.9 mg NO₂ ^–-N kg^–1) and thus of minor importance with respect to the persistent inhibition after NH₄ ⁺ or urea application. CH₄ oxidation after NaNO₃ (40 mg N kg^–1) and NaCl addition did not differ to that of the untreated soil. The effect of organic manures on CH₄ oxidation depended on their C/N ratio: fresh sugar beet leaves enhanced mineralization, which caused an instantaneous 20% inhibition, whereas after wheat straw application available soil N was rapidly immobilized and no effect on CH₄ oxidation was found. The 28% increase in CH₄ oxidation after biowaste compost application was not related to its C/N ratio and was probably the result of an inoculation with methanotrophic bacteria. Only with high NH₄ ⁺ application rates (240 mg N kg^–1) could the persistent inhibitory effect partly be attributed to a pH decrease during nitrification. The exact reason for the observed persistent inhibition after a single, moderate NH₄ ⁺ or urea application is still unknown and merits further study. Received: 31 October 1997     

灌溉施用氮肥后氮素在土壤中的转化及淋失状况: 土柱模拟研究

A soil column method was used to compare the effect of drip fertigation (the application of fertilizer through drip irrigation systems, DFI) on the leaching loss and transformation of urea-N in soil with that of surface fertilization combined with flood irrigation (SFI), and to study the leaching loss and transformation of three kinds of nitrogen fertilizers (nitrate fertilizer, ammonium fertilizer, and urea fertilizer) in two contrasting soils after the fertigation. In comparison to SFI, DFI decreased leaching loss of urea-N from the soil and increased the mineral N (NH₄⁺-N + NO₃^--N) in the soil. The N leached from a clay loam soil ranged from 5.7% to 9.6% of the total N added as fertilizer, whereas for a sandy loam soil they ranged between 16.2% and 30.4%. Leaching losses of mineral N were higher when nitrate fertilizer was used compared to urea or ammonium fertilizer. Compared to the control (without urea addition), on the first day when soils were fertigated with urea, there were increases in NH₄⁺-N in the soils. This confirmed the rapid hydrolysis of urea in soil during fertigation. NH₄⁺-N in soils reached a peak about 5 days after fertigation, and due to nitrification it began to decrease at day 10. After applying NH₄⁺-N fertilizer and urea and during the incubation period, the mineral nitrogen in the soil decreased. This may be related to the occurrence of NH₄⁺-N fixation or volatilization in the soil during the fertigation process.     

Land use affects the distribution of soil inorganic nitrogen in smallholder production systems in Kenya

 We hypothesized that the integration of trees and shrubs in agricultural landscapes can reduce NO₃ ^– leaching and increase utilization of subsoil N. A field survey was conducted on 14 farms on acid soils in the subhumid highlands of Kenya, where there is little use of fertilizers, to determine the effect of vegetation types (VT) on soil NH₄ ⁺ and NO₃ ^– to 4 m depth. The VT included maize (Zea mays) with poor growth and good growth, Markhamia lutea trees scattered in maize, natural weed fallow, banana (Musa spp.), hedgerow, and eucalyptus woodlot. The effect of VT on NH₄ ⁺ was small (<1 mg N kg^–1). NO₃ ^– within a VT was about constant with depth below 0.25 m, but subsoil NO₃ ^– varied greatly among VT. Mean NO₃ ^–-N concentrations at 0.5–4 m depth were low beneath hedgerow and woodlot (<0.2 mg kg^–1), intermediate beneath weed fallow (0.2–0.7 mg kg^–1), banana (0.5–1.0 mg kg^–1) and markhamia (0.5–1.6 mg kg^–1), and high beneath both poor (1.0–2.1 mg kg^–1) and good (1.9–3.1 mg kg^–1) maize. Subsoil NO₃ ^– (0.5–4 m) was agronomically significant after maize harvest with 37 kg N ha^–1 m^–1 depth of subsoil beneath good maize and 27 kg N ha^–1 m^–1 depth beneath poor maize. In contrast, subsoil NO₃ ^– was only 2 kg N ha^–1 m^–1 depth beneath woodlot and hedgerow. These results demonstrate that the integration of perennial vegetation and the rotation of annual and perennial crops can tighten N cycling in agricultural landscapes. Received: 8 July 1999     

Variation in the relationship between nitrification and acidification of subtropical soils as affected by the addition of urea or ammonium sulfate

The effects on nitrification and acidification in three subtropical soils to which (NH₄)₂SO₄ or urea had been added at rate of 250 mg N kg⁻¹ was studied using laboratory-based incubations. The results indicated that NH₄⁺ input did not stimulate nitrification in a red forest soil, nor was there any soil acidification. Unlike red forest soil, (NH₄)₂SO₄ enhanced nitrification of an upland soil, whilst urea was more effective in stimulating nitrification, and here the soil was slightly acidified. For another upland soil, NH₄⁺ input greatly enhanced nitrification and as a result, this soil was significantly acidified. We conclude that the effects of NH₄⁺ addition on nitrification and acidification in cultivated soils would be quite different from in forest soils. During the incubation, N isotope fractionation was closely related to the nitrifying capacity of the soils.     

The effect of water movement on the transport of dicyandiamide,ammonium and urea in unsaturated soils

A laboratory experiment was conducted to investigate the relative mobility of dicyandiamide (DCD) and jointly applied ammoniacal salts or urea in three different soils of lower Egypt, and to determine the extent to which DCD separates from N-fertilizer in unsaturated soil undergoing leaching. The experimental results suggest that, under conditions of water flow, DCD is readily separated from NH₄⁺ but parts from urea to a far lesser extent. The large difference in mobility between DCD and NH₄⁺ should severely limit the effectiveness of DCD as a nitrification inhibitor in the three soils considered when applied in conjunction with ammoniacal salts. In two out of three cases, the situation is similarly unfavorable in the case of joint DCD and urea application. However, the observation that DCD, in a low CEC sandy loam, moves within the soil solution at a slightly lower rate than urea suggests that joint application with urea would keep at least part of the DCD in contact with the NH₄⁺ ions and, therefore, would preserve some of the effectiveness of DCD under leaching conditions in this soil.     

Chemical and biological characteristics of alkaline saline soils from the former Lake Texcoco as affected by artificial drainage

 Soils from the former Lake Texcoco are alkaline saline and were artificially drained and irrigated with sewage effluents since the late 1980s. Undrained soil and soil drained for 1, 5 and 8 years were sampled, characterized and incubated aerobically for 90 days at 22±1  °C while production of CO₂, available P and concentrations of NH₄ ⁺, NO₂ ^– and NO₃ ^– were monitored. Artificial drainage decreased pH_H2O, water holding capacity, organic C, total N, and Na⁺, K⁺, Mg²⁺, B, Cl^– and SO₄ ^2– concentrations, increased inorganic C and Ca²⁺ concentrations more than 5-fold while total P was not affected. Microbial biomass C decreased with increased length of drainage but bacteria, actinomycetes, denitrifiers and cellulose-utilizing bacteria tended to show opposite trends. CO₂ production was less in soils drained ≥5 years compared to undrained soil but more than in soils drained for 1 year. Emission of NH₃ was negligible and concentrations of NH₄ ⁺ remained constant over time in each soil. Nitrification, as witnessed by increases in NO₃ ^– concentrations, occurred in soil drained for 8 years. NO₂ ^– concentrations decreased in soils drained ≤1 year in the first 7 days of the incubation and remained constant thereafter. It was found that artificial drainage of soils from the former Lake Texcoco profoundly affected soil characteristics. Decreases in pH and Na⁺, K⁺, Cl^– and SO₄ ^2– concentrations made conditions more favourable for plant growth, although low concentrations of inorganic N and available P might be limiting factors. Received: 1 December 1999     

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     

Impact of land-use types on soil nitrogen net mineralization in the sandstorm and water source area of Beijing,China

Changes of land-use type (LUT) can affect soil nutrient pools and cycling processes that relate long-term sustainability of ecosystem, and can also affect atmospheric CO₂ concentrations and global warming through soil respiration. We conducted a comparative study to determine NH₄⁺ and NO₃⁻ concentrations in soil profiles (0–200 cm) and examined the net nitrogen (N) mineralization and net nitrification in soil surface (0–20 cm) of adjacent naturally regenerated secondary forests (NSF), man-made forests (MMF), grasslands and cropland soils from the windy arid and semi-arid Hebei plateau, the sandstorm and water source area of Beijing, China. Cropland and grassland soils showed significantly higher inorganic N concentrations than forest soils. NO₃⁻-N accounted for 50–90% of inorganic N in cropland and grassland soils, while NH₄⁺-N was the main form of inorganic N in NSF and MMF soils. Average net N-mineralization rates (mg kg⁻¹ d⁻¹) were much higher in native ecosystems (1.51 for NSF soils and 1.24 for grassland soils) than in human disturbed LUT (0.15 for cropland soils and 0.85 for MMF soils). Net ammonification was low in all the LUT while net nitrification was the major process of net N mineralization. For more insight in urea transformation, the increase in NH₄⁺ and, NO₃⁻ concentrations as well as C mineralization after urea addition was analyzed on whole soils. Urea application stimulated the net soil C mineralization and urea transformation pattern was consistent with net soil N mineralization, except that the rate was slightly slower. Land-use conversion from NSF to MMF, or from grassland to cropland decreased soil net N mineralization, but increased net nitrification after 40 years or 70 years, respectively. The observed higher rates of net nitrification suggested that land-use conversions in the Hebei plateau might lead to N losses in the form of nitrate.