Effect of urease and nitrification inhibitors on N transformation, gaseous emissions of ammonia and nitrous oxide, pasture yield and N uptake in grazed pasture system

Nitrogen (N) losses via nitrate (NO₃⁻) leaching, ammonia (NH₃) volatilization and nitrous oxide (N₂O) emissions from grazed pastures in New Zealand are one of the major contributors to environmental degradation. The use of N inhibitors (urease and nitrification inhibitors) may have a role in mitigating these N losses. A one-year field experiment was conducted on a permanent dairy-grazed pasture site at Massey University, Palmerston North, New Zealand to quantify these N losses and to assess the effect of N inhibitors in reducing such losses during May 2005-2006. Cow urine at 600 kg N ha⁻¹ rate with or without urease inhibitor N-(n-butyl) thiophosphoric triamide (nBTPT) or (trade name “Agrotain”) (3 L ha⁻¹), nitrification inhibitor dicyandiamide (DCD) (7 kg ha⁻¹) and the use of double inhibitor (DI) containing a combination of both Agrotain and DCD (3:7) were applied to field plots in autumn, spring and summer. Pasture production, NH₃ and N₂O fluxes, soil mineral N concentrations, microbial biomass C and N, and soil pH were measured following the application of treatments during each season. All measured parameters, except soil microbial biomass C and N, were influenced by the added inhibitors during the three seasons. Agrotain reduced NH₃ emissions over urine alone by 29%, 93% and 31% in autumn, spring and summer respectively but had little effect on N₂O emission. DCD reduced N₂O emission over urine alone by 52%, 39% and 16% in autumn, spring and summer respectively but increased NH₃ emission by 56%, 9% and 17% over urine alone during those three seasons. The double inhibitor reduced NH₃ by 14%, 78% and 9% and N₂O emissions by 37%, 67% and 28% over urine alone in autumn, spring and summer respectively. The double inhibitor also increased pasture dry matter by 10%, 11% and 8% and N uptake by the 17%, 28% and 10% over urine alone during autumn, spring and summer respectively. Changes in soil mineral N and pH suggested a delay in urine-N hydrolysis with Agrotain, and reduced nitrification with DCD. The combination of Agrotain and DCD was more effective in reducing both NH₃ and N₂O emissions, improving pasture production, controlling urea hydrolysis and retaining N in NH₄⁺ form. These results suggest that the combination of both urease and nitrification inhibitors may have the most potential to reduce N losses if losses are associated with urine and improve pasture production in intensively grazed systems.     

Emissions of CO2 and N2O from a pasture soil from Madagascar—Simulating conversion to direct‐seeding mulch‐based cropping in incubations with organic and inorganic inputs

In the highlands of Madagascar, agricultural expansion gained on grasslands and cropping systems based on direct seeding with permanent vegetation cover are emerging as a means to sustain upland crop production. The objective of this study was to examine how such agricultural practices affect greenhouse‐gas emissions from a loamy Ferralsol previously used as a pasture. We conducted an experiment under controlled laboratory conditions combining cattle manure, crop residues (rice straw), and mineral fertilizers (urea plus NPK or di‐NH₄‐phosphate) to mimic on‐field inputs and examined soil CO₂ and N₂O emissions during a 28‐d incubation at low and high water‐filled pore space (40% and 90% WFPS). Emissions of N₂O from the control soil, i.e., soil receiving no input, were extremely small (< 5 ng N₂O‐N (g soil)^–1 h^–1) even under anaerobic conditions. Soil moisture did not affect the order of magnitude of CO₂ emissions while N₂O fluxes were up to 46 times larger at high soil WFPS, indicating the potential influence of denitrification under these conditions. Both CO₂ and N₂O emissions were affected by treatments, incubation time, and their interactions. Crop‐residue application resulted in larger fluxes of CO₂ but reduced N₂O emissions probably due to N immobilization. The use of di‐NH₄‐phosphate was a better option than NPK to reduce N₂O emissions without increasing CO₂ fluxes when soil received mineral fertilizers. Further studies are needed to translate the findings to field conditions and relate greenhouse‐gas budgets to crop production.     

Effects of biochar,urea and their co‐application on nitrogen mineralization in soil and growth of Chinese cabbage

Experiments were conducted to study the effect of soil applications of kunai grass (Imperata cylindrica) biochar (0 and 10 t/ha) and laboratory grade urea (0, 200 and 500 kg N/ha) and their co‐application on nitrogen (N) mineralization in an acid soil. The results of an incubation study showed that the biochar only treatment and co‐application with urea at 200 kg N/ha could impede transformation of urea to ammonium‐N (NH₄⁺‐N). Soil application of biochar together with urea at 500 kg N/ha produced the highest nitrate‐N (NO₃^?‐N) and mineral N concentrations in the soil over 90 days. Co‐application of urea N with biochar improved soil N mineralization parameters such as mineralization potential (N_A) and coefficient of mineralization rate (k) compared to biochar alone. In a parallel study performed under greenhouse conditions, Chinese cabbage (Brassica rapa L. ssp. chinensis L.) showed significantly greater (P < 0.05) marketable fresh weight, dry matter production and N uptake in soil receiving urea N at 500 kg/ha or co‐application of biochar with urea N compared to the control. Application of biochar only or urea only at 200 kg N/ha did not offer any short‐term agronomic advantages. The N use efficiency of the crop remained unaffected by the fertilizer regimes. Applications of biochar only at 10 t/ha did not offer benefits in this tropical acid soil unless co‐applied with sufficient urea N.     

What artificial urine composition is adequate for simulating soil N2O fluxes and mineral N dynamics?

Artificial urine, an aqueous solution of various nitrogenous compounds and salts, is routinely used in soil incubation studies on nitrous oxide (N₂O) emissions and related nitrogen (N) and pH dynamics. There is, however, no consensus on artificial urine composition, and a wide variety of compositions are used. The aim of this study was to test which artificial urine composition is adequate for simulating N₂O fluxes, respiration, soil mineral N and pH dynamics of real cattle urine in both short- and long-term incubation studies. Urine solutions of differing compositions were applied to a sandy soil and incubated for 65 days, and results of measurements on N₂O fluxes and soil mineral N were analyzed over the first 5 days as well as over the whole incubation period. Results from two real cattle urines with known nitrogenous composition (R1 and R2) were compared with three artificial urine types: (i) urea+glycine (AG), (ii) urea+hippuric acid (AH) and (iii) an artificial urine identical to the nitrogenous composition of real urine R1 (AR). During the first 5 days, only cumulative N₂O emissions for AG deviated significantly (P=0.02) from the N₂O emissions for real urines, with 0.4% of applied N emitted compared with 0.0% and 0.1% for R1 and R2, respectively. Respiration from R1 was significantly (P<0.001) higher than from R2 and all artificial urines. Over the whole incubation period, no significant differences could be detected for N₂O emissions or respiration with urine type. From all artificial urine types, AH yielded N₂O emissions closest to those from real urine. AG deviated most from real urine, both in short- and long-term incubations. Over the whole period, soil NH₄⁺ was higher for all artificial urines (P<0.001) and pH-KCl was lower for AG and AR (P=0.004) than for the real urines. AH was not significantly different from real urine R2 with respect to all measured properties except soil NH₄⁺. We conclude that only AG did not adequately simulate N₂O emissions, and that glycine is therefore not an appropriate substitution for hippuric acid in artificial urine. For future studies using artificial urine we recommend therefore a mixture containing at least urea and hippuric acid as sources of N. As no artificial urine composition resembled real urine with respect to all measured variables, even when nitrogenous composition was identical (AR), we recommend the use of real urines whenever possible.     

Formation of hybrid N2O in a suspended soil due to co‐denitrification of NH2OH

A few studies have shown that amine compounds (e.g., hydroxylamine) can be co‐metabolically introduced into the reaction pathway of denitrification. During this microbial process, the N atom of the amine species is bound to a N atom of nitrite. In case of hydroxylamine, this concomitant reaction ultimately results in the formation of hybrid N₂O. Due to its co‐metabolic character the process has been termed co‐denitrification. Hybrid N₂O production during co‐denitrification has been proven to occur in prokaryotic (e.g., Pseudomonas sp.) as well as eukaryotic (e.g., Fusarium sp.) species. Many of them are already well‐known as common denitrifiers. However, until now no clear evidence has been provided to show that N₂O production by co‐denitrification really takes place in a soil. In the present study, a formation of hybrid N₂O was revealed by an adapted ¹⁵N‐tracer model, when both hydroxylamine and ¹⁵N‐nitrate were applied (mol ratio 10:1) to an anaerobically incubated soil suspension from a Haplic Chernozem. The presence of hybrid N₂O was also indicated by a novel characteristic factor (R_binom) developed for a hybrid‐N‐N‐gas detection. By contrast, no hybrid N₂O was found when either an autoclaved soil suspension, only nitrate or only hydroxylamine was used. Thus, it appears that hybrid‐N₂O formation occurred due to co‐denitrification of hydroxylamine. Hence, this is the first study which demonstrates hybrid‐N₂O production by co‐denitrification beyond a microbial species level. The ¹⁵N‐tracer model revealed that under the given experimental conditions N₂O production by co‐denitrification prevailed against N₂O from denitrification and abiotic hydroxylamine decomposition. In addition, a formation of hybrid N₂ was also calculated by the model. However, the experimental results lead to the conclusion that it was most likely caused by a reduction of hybrid N₂O due to conventional denitrification.     

Presubmergence and green manure affect the transformations of nitrogen‐15‐labeled urea under lowland soil conditions

The effect of presubmergence and green manuring on various processes involved in [¹⁵N]‐urea transformations were studied in a growth chamber after [¹⁵N]‐urea application to floodwater. Presubmergence for 14 days increased urea hydrolysis rates and floodwater pH, resulting in higher NH₃ volatilization as compared to without presubmergence. Presubmergence also increased nitrification and subsequent denitrification but lower N assimilation by floodwater algae caused higher gaseous losses. Addition of green manure maintained higher NH₄⁺‐N concentration in floodwater mainly because of lower nitrification rates but resulted in highest NH₃ volatilization losses. Although green manure did not affect the KCl extractable NH₄⁺‐N from applied fertilizer, it maintained higher NH₄⁺‐N content due to its decomposition and increased mineralization of organic N. After 32 days about 36.9 % (T₁), 23.9 % (T₂), and 36.4 % (T₃) of the applied urea N was incorporated in the pool of soil organic N in treatments. It was evident that the presubmergence has effected the recovery of applied urea N.     

Quantification of N2 fixation and annual N benefit from N2 fixation in soybean accrued to the soil under soybean‐wheat continuous rotation

A computational exercise was undertaken to quantify the percent N derived from atmosphere %Ndfa) in soybean and consequent N benefit from biological N₂‐fixation process annually accrued to the soil by the soybean crop using average annual N‐input/‐output balance sheet from a 7 yr old soybean‐wheat continuous rotational experiment on a Typic Haplustert. The experiment was conducted with 16 treatments comprised of combinations of four annual rates of farmyard manure (FYM ? 0, 4, 8, and 16 t ha^–1) and four annual rates of fertilizer N (? 0, 72.5, 145, and 230 kg N ha^–1) applications. The estimated N contributed through residual biomass of soybean (RBN_S) consisting of leaf fall, root, nodules, and rhizodeposition varied in the ranges of 7.02–16.94, 11.65–28.83, 3.31–8.91, and 11.3–23.8 kg N ha^–1 yr^–1, respectively. A linear relationship was observed between RBN_S and harvested biomass N (HBN_S) of soybean in the form of RBN_S = 0.461 × HBN_S – 20.67 (r = 0.989, P < 0.01), indicating that for each 100 kg N assimilated by the harvested biomass of soybean, 25.4 kg N was added to the soil through residual biomass. The Ndfa values ranged between 13% and 81% depending upon the annual rates of application of fertilizer N and FYM. As per the main effects, the %Ndfa declined from 76.4 to 26.0 with the increase in annual fertilizer‐N application from 0 to 230 kg N ha^–1, whereas %Ndfa increased from 40.8 to 65.8 with the increase in FYM rates from 0 to 16 t ha^–1, respectively. The N benefit from biological N₂ fixation accrued to the soil through residual biomass of soybean ranged from 7.6 to 53.7 kg N ha^–1 yr^–1. The treatments having %Ndfa values higher than 78 showed considerable annual contribution of N from N₂ fixation to the soil which were sufficient enough to offset the quantity of N removed from the soil (i.e., native soil N / FYM‐N / fertilizer‐N) with harvested biomass of soybean.     

Carbon dioxide and gaseous nitrogen emissions from biochar‐amended soils under wastewater irrigated urban vegetable production of Burkina Faso and Ghana

To quantify carbon (C) and nitrogen (N) losses in soils of West African urban and peri‐urban agriculture (UPA) we measured fluxes of CO₂‐C, N₂O‐N, and NH₃‐N from irrigated fields in Ouagadougou, Burkina Faso, and Tamale, Ghana, under different fertilization and (waste‐)water regimes. Compared with the unamended control, application of fertilizers increased average cumulative CO₂‐C emissions during eight cropping cycles in Ouagadougou by 103% and during seven cropping cycles in Tamale by 42%. Calculated total emissions measured across all cropping cycles reached 14 t C ha^?1 in Ouagadougou, accounting for 73% of the C applied as organic fertilizer over a period of two years at this site, and 9 t C ha^?1 in Tamale. Compared with unamended control plots, fertilizer application increased N₂O‐N emissions in Ouagadougou during different cropping cycles, ranging from 37 to 360%, while average NH₃‐N losses increased by 670%. Fertilizer application had no significant effects on N₂O‐N losses in Tamale. While wastewater irrigation did not significantly enhance CO₂‐C emissions in Ouagadougou, average CO₂‐C emissions in Tamale were 71% (1.6 t C ha^?1) higher on wastewater plots compared with those of the control (0.9 t C ha^?1). However, no significant effects of wastewater on N₂O‐N and NH₃‐N emissions were observed at either location. Although biochar did not affect N₂O‐N and NH₃‐N losses, the addition of biochar could contribute to reducing CO₂‐C emissions from urban garden soils. When related to crop production, CO₂‐C emissions were higher on control than on fertilized plots, but this was not the case for absolute CO₂‐C emissions.     

Controlled‐release urea decreased ammonia volatilization and increased nitrogen use efficiency of cotton

Excessive nitrogen (N) fertilizer input leads to higher N loss via ammonia (NH₃) volatilization. Controlled‐release urea (CRU) was expected to reduce emission losses of N. An incubation and a plant growth experiment with Gossypium hirsutum L. were conducted with urea and CRU (a fertilizer mixture of polymer‐coating sulfur‐coated urea and polymer‐coated urea with N ratios of 5 : 5) under six levels of N fertilization rates, which were 0% (0 mg N kg⁻¹ soil), 50% (110 mg N kg⁻¹ soil), 75% (165 mg N kg⁻¹ soil), 100% (220 mg N kg⁻¹ soil), 125% (275 mg N kg⁻¹ soil), and 150% (330 mg N kg⁻¹ soil) of the recommended N fertilizer rate. For each type of N fertilizer, the NH₃ volatilization, cotton yield, and N uptake increased with the rate of N application, while N use efficiency reached a threshold and decreased when N application rates of urea and CRU exceeded 238.7 and 209.3 mg N kg⁻¹ soil, respectively. Ammonia volatilization was reduced by 65–105% with CRU in comparison to urea treatments. The N release characteristic of CRU corresponded well to the N requirements of cotton growth. Soil inorganic N contents, leaf SPAD values, and net photosynthetic rates were increased by CRU application, particularly from the full bloom stage to the initial boll‐opening stage. As a result, CRU treatments achieved significantly higher lint yield by 7–30%, and the N use efficiency of CRU treatments was increased by 25–124% relative to that of urea treatments. These results suggest that the application of CRU could be widely used for cotton production with higher N use efficiency and lower NH₃ volatilization.     

Estimating symbiotic N2 fixation in Robinia pseudoacacia

Estimating symbiotic di‐nitrogen (N₂) fixation is challenging, especially when working with woody N₂ fixers in field trials. Fortunately, isotope methods based on ¹⁵N natural abundance or on ¹⁵N artificial enrichment (dilution method) make it possible to estimate the proportion of nitrogen derived from the atmosphere (Ndfa) in N₂‐fixing species. These methods have been extensively used in the field for herbaceous species, much less for tree species such as alder and acacia, and rarely for black locust (Robinia pseudoacacia). The objectives of this study were to characterize the fixation potential of black locust in a plantation by using the two ¹⁵N isotope methods in the field, and to document values of isotope fractionation occurring during N₂ fixation (the B value). B values were estimated both by growing trees on an N‐free medium in controlled conditions (B_lab) and by making Ndfa calculated with the natural abundance method converge with Ndfa calculated with the ¹⁵N dilution method in the field (B_field). The two methods gave consistent estimates of the B value. B values ranging between –1.4 and –3.2‰ were found, varying with the age of the plant material. Up to 76% of the N in the black locust trees came from the atmosphere, representing more than 45 kg N ha^?1 over five years and confirming that black locust may be well adapted to N‐poor soils.     

Combined effects of nitrogen deposition and biochar application on emissions of N2O,CO2 and NH3 from agricultural and forest soils

Abstract

Both nitrogen (N) deposition and biochar can affect the emissions of nitrous oxide (N₂O), carbon dioxide (CO₂) and ammonia (NH₃) from different soils. Here, we have established a simulated wet N deposition experiment to investigate the effects of N deposition and biochar addition on N₂O and CO₂ emissions and NH₃ volatilization from agricultural and forest soils. Repacked soil columns were subjected to six N deposition events over a 1-year period. N was applied at rates of 0 (N0), 60 (N60), and 120 (N120) kg Nh a^?1 yr^?1 without or with biochar (0 and 30 t ha^?1 yr^?1). For agricultural soil, adding N increased cumulative N₂O emissions by 29.8% and 99.1% (p < 0.05) from the N60 and N120 treatments, respectively as compared to without N treatments, and N120 emitted 53.4% more (p < 0.05) N₂O than the N60 treatment; NH₃ volatilization increased by 33.6% and 91.9% (p < 0.05) from the N60 and N120 treatments, respectively, as compared to without N treatments, and N120 emitted 43.6% more (p < 0.05) NH₃ than N60; cumulative CO₂ emissions were not influenced by N addition. For forest soil, adding N significantly increased cumulative N₂O emissions by 141.2% (p < 0.05) and 323.0% (p < 0.05) from N60 and N120 treatments, respectively, as compared to without N treatments, and N120 emitted 75.4% more (p < 0.05) N₂O than N60; NH₃ volatilization increased by 39.0% (p < 0.05) and 56.1% (p < 0.05) from the N60 and N120 treatments, respectively, as compared to without N treatments, and there was no obvious difference between N120 and N60 treatments; cumulative CO₂ emissions were not influenced by N addition. Biochar amendment significantly (p < 0.05) decreased cumulative N₂O emissions by 20.2% and 25.5% from agricultural and forest soils, respectively, and increased CO₂ emissions slightly by 7.2% and NH₃ volatilization obviously by 21.0% in the agricultural soil, while significantly decreasing CO₂ emissions by 31.5% and NH₃ volatilization by 22.5% in the forest soil. These results suggest that N deposition would strengthen N₂O and NH₃ emissions and have no effect on CO₂ emissions in both soils, and treatments receiving the higher N rate at N120 emitted obviously more N₂O and NH₃ than the lower rate at N60. Under the simulated N deposition circumstances, biochar incorporation suppressed N₂O emissions in both soils, and produced contrasting effects on CO₂ and NH₃ emissions, being enhanced in the agricultural soil while suppressed in the forest soil.     

Effect of crop residue C:N ratio on N2O emissions from Gray Lowland soil in Mikasa,Hokkaido, Japan

Abstract

We studied the effect of crop residues with various C:N ratios on N₂O emissions from soil. We set up five experimental plots with four types of crop residues, onion leaf (OL), soybean stem and leaf (SSL), rice straw (RS) and wheat straw (WS), and no residue (NR) on Gray Lowland soil in Mikasa, Hokkaido, Japan. The C:N ratios of these crop residues were 11.6, 14.5, 62.3, and 110, respectively. Based on the results of a questionnaire survey of farmer practices, we determined appropriate application rates: 108, 168, 110, 141 and 0 g C m^?2 and 9.3, 11.6, 1.76, 1.28 and 0 g N m^?2, respectively. We measured N₂O, CO₂ and NO fluxes using a closed chamber method. At the same time, we measured soil temperature at a depth of 5 cm, water-filled pore space (WFPS), and the concentrations of soil NH⁺ ₄-N, NO^? ₃-N and water-soluble organic carbon (WSOC). Significant peaks of N₂O and CO₂ emissions came from OL and SSL just after application, but there were no emissions from RS, WS or NR. There was a significant relationship between N₂O and CO₂ emissions in each treatment except WS, and correlations between CO₂ flux and temperature in RS, soil NH⁺ ₄-N and N₂O flux in SSL and NR, soil NH⁺ ₄-N and CO₂ flux in SSL, and WSOC and CO₂ flux in WS. The ratio of N₂O-N/NO-N increased to approximately 100 in OL and SSL as N₂O emissions increased. Cumulative N₂O and CO₂ emissions increased as the C:N ratio decreased, but not significantly. The ratio of N₂O emission to applied N ranged from ?0.43% to 0.86%, and was significantly correlated with C:N ratio (y = ?0.59 ln [x] + 2.30, r ² = 0.99, P < 0.01). The ratio of CO₂ emissions to applied C ranged from ?5.8% to 45% and was also correlated with C:N ratio, but not significantly (r ² = 0.78, P = 0.11).     

N2O, NH3 and NOx Emissions as a Function of Urea Granule Size and Soil Type Under Aerobic Conditions

We examined the influence of various urea granule sizes (< 2, 7.0, 9.9 and 12.7 mm) applied into a silt loam soil (experiment 1) and soil types (sandy, silt and clay loam) treated with the largest granule (experiment 2) on gaseous N loss (except N₂) at field capacity. The prilled urea (PU) was mixed into the soil whereas the urea granules were point-placed at a 5.0-cm depth. For experiment 1, N₂O emission was enhanced with increasing granule size, ranging from 0.17–0.50% of the added N during the 45-day incubation period. In the case of experiment 2, the sandy loam soil (0.59%) behaved similarly with the silt loam (0.53%) but both showed remarkably lower emissions than were found for the clay loam soil (2.61%). Both nitrification and N₂O emissions were delayed by several days with increasing granule size, and the latter was influenced by mineral N, soil water and pH. By contrast, the NH₃ volatilization decreased with increasing granule size, implying the inhibition of urease activity by urea concentration gradients. Considering both experimental results, the NH₃ loss was highest for the PU-treated (1.73%) and the larger granules regardless of soil type did not emit more than 0.27% of the added N over 22 days, possibly because the high concentrations of either mineral N or NH₄ ⁺ in the soil surface layer (0–2.5 cm) and the high H₊ buffering capacity might regulate the NH₃ emission. Similar to the pattern of NH₃ loss, NO_x emission was noticeably higher for the PU-treated soil (0.97%) than for the larger granule sizes (0.09–0.29%), which were the highest for the sandy and clay loam soils. Positional differences in the concentration of mineral N and nitrification also influenced the NO_x emission. As such, total NH₃ loss was proportional to total NO_x emission, indicating similar influence of soil and environmental conditions on both. Pooled total N₂O, NH₃ and NO_x emission data suggest that the PU-treated soil could induce greater gaseous N loss over larger urea granules, largely in the form of NH₃ and NO_x emissions, whereas a similar increase with the largest granule size was mainly due to the total N₂O flux.     

Responses of photosynthesis,chlorophyll fluorescence,and grain yield of maize to controlled‐release urea and irrigation after anthesis

Controlled‐release urea (CRU) is a new type of urea, which may increase crop nitrogen (N)‐use efficiency compared with conventional urea (CU), but the conditions where it outperforms urea are not well defined. A field experiment assessing responses of plant growth and grain yield of maize to CRU and irrigation was conducted on a typical agricultural farm in Shandong, China. Five treatments of the two types of urea (75, 150 kg N ha^–1, 0 kg N ha^–1) were applied as basal fertilizer when sowing maize, and two water treatments (W₀ and W₁) were used 23 d after anthesis. Net photosynthetic rate (P_N) and chlorophyll concentration as well as leaf‐area index (LAI) increased significantly by both CRU and CU application, with the increases being larger in CRU‐treated plants than in CU‐treated plants at grain filling and maturing stages. CRU significantly enhanced the maximum photochemical efficiency (F_v / F_m), PSII coefficient of photochemical fluorescence quenching (q_P), and actual quantum yield of PSII electron transformation (Φ_PSII) but decreased the nonphotochemical quenching (NPQ). Cob‐leaf N concentration of CRU‐treated plants was significantly higher than that of CU‐treated plants under no irrigation, but not in the irrigation treatment 30 d after anthesis. Significant positive correlations were found between cob‐leaf N concentration and P_N both with and without irrigation. Grain yield of maize was significantly higher in the CRU treatment than in the CU treatment under both irrigation conditions. In conclusion, CRU as a basal application appeared to increase the N‐use efficiency for maize relative to CU especially by maintaining N supply after anthesis.     

Nitrat‐Austräge auf intensiv und extensiv beweidetem Grünland,erfasst mittels Saugkerzen‐ und Nmin‐Beprobung II Variabilität der NO3‐ und NH4‐Werte und Aussagegenauigkeit der Messmethoden

Nitrate leaching from intensively and extensively grazed grassland measured with suction cup samplers and sampling of soil mineral‐N II Variability of NO₃ and NH₄ values and degree of accuracy of the measurement methods Data from a grazing experiment — comparison of mean values, see Anger et al. (2002) — were used to estimate within‐field variability to asses the accuracy of two frequently used methods of estimating NO₃ leaching on pastures: (1) the ceramic suction cup sampling (with 34 cups ha^—1 minimum, calculated climatic water balance, 4 leaching periods) and (2) using the soil mineral‐N method (vertical soil NO₃ and NH₄ content in 0—0.9 m (N_min) measured at the beginning and end of two winters on a minimum of 10 different areas of 50 m² each with a minimum of 7 different sample cores). These methods were used on two permanent pastures with high mean stocking density of cattle of 4.9 LU ha^—1 on 1.3 ha with N‐fertilization of 250 kg N ha^—1 (= intensive [I]) and 2.9 LU without N fertilization on a 2.2 ha pasture (= extensive [E]). The results show that NO₃ leaching on pastures was largely due to few selectively extremely high NO₃ amounts under a few excrement spots — mainly urine spots — which would not be sampled representatively with an acceptable effort in a conventional grazing experiment. In both grazing treatments, very large spatial variation occurred. This was greater between the different suction cups than between the compound mineral N samples of each area. Therefore, a marked skewness and kurtosis demonstrated a non‐normal distribution of samples from suction cups, while mineral N values did not show this effect consistently. Sampling selected mostly spots without noticeable influence of excrement, but a few samples with very high values identified evidently urine spots from summer or autumn grazing. The differences in mean coefficient of variation (CV) between the grazing treatments and estimation methods were mainly based on the stocking rate and the density of excrement spots. CV values were 131 % [I] / 242 % [E] for NO₃ leaching measured with suction cup samplers and of 71 % [I] / 116 % [E] for soil NO₃ values and 24 % [I] / 34 % [E] for soil NH₄ values in 0—0.9 m according N_min‐method. Results of the N_min method are obviously inaccurate even with a sampling intensity much greater than 70 cores ha^—1; and so making an estimation of NO₃ leaching by this method is unsatisfactory for pastures. Compared to this, the results of suction cup sampling are more convincing; but even with a tolerated deviation of ± 20 % from the empirically estimated average and with a 95 %‐confidence interval, the calculated mean minimum number of samples in our experiment should be increased to 146 and 265 suction cups ha^—1 for the intensively and extensively grazed treatments, respectively. This requirement would be prohibitive for many field experiments.     

Gaseous emissions of nitrogen and carbon from urban vegetable gardens in Bobo‐Dioulasso,Burkina Faso

Urban and peri‐urban agriculture (UPA) is an important livelihood strategy for the urban poor in sub‐Saharan Africa and contributes to meeting increasing food demands in the rapidly growing cities. Although in recent years many research activities have been geared towards enhancing the productivity of this land‐use system, little is known about turnover processes and nutrient efficiency of UPA. The aim of our study therefore was to determine horizontal fluxes of N, P, K, and C as well as gaseous N and C emissions in urban vegetable gardens of Bobo‐Dioulasso, Burkina Faso. Two gardens referred to as “Kodéni” and “Kuinima” were selected as representative for urban and peri‐urban systems classified as: (1) “commercial gardening + field crops and livestock system” and (2) “commercial gardening and semicommercial field crop system”, respectively. A nutrient‐balance approach was used to monitor matter fluxes from March 2008 to March 2009 in both gardens. Ammonia (NH₃), nitrous oxide (N₂O) and carbon dioxide (CO₂) emissions from the respective soils were measured during the coolest and the hottest period of the day using a closed‐chamber system. Annual partial balances amounted to 2056 kg N ha^–1, 615 kg P ha^–1, 1864 kg K ha^–1, and 33 893 kg C ha^–1 at Kodéni and to 1752 kg N ha^–1, 446 kg P ha^–1, 1643 kg K ha^–1, and 21 021 kg C ha^–1 at Kuinima. Emission rates were highest during the hot midday hours with peaks after fertilizer applications when fluxes of up to 1140 g NH₃‐N ha^–1 h^–1, 154 g N₂O‐N ha^–1 h^–1, 12 993 g CO₂‐C ha^–1 h^–1 were recorded for Kodéni and Kuinima. Estimated annual gaseous N (NH₃‐N + N₂O‐N) and C (CO₂‐C + CH₄‐C) losses reached 419 kg N ha^–1 and 35 862 kg C ha^–1 at Kodéni and 347 kg N ha^–1 and 22 364 kg C ha^–1 at Kuinima. For both gardens, this represented 20% and 106% of the N and C surpluses, respectively. Emissions of NH₃, largely emitted after surface application of manure and mineral fertilizers, accounted for 73% and 77% of total estimated N losses for Kodéni and Kuinima. To mitigate N losses nutrient‐management practices in UPA vegetable production of Bobo‐Dioulasso would greatly benefit from better synchronizing nutrient‐input rates with crop demands.     

Evaluation of isotopic dilution method for measuring N2 fixation in Azolla: Comparison with other methods 1

An isotopic dilution method that overcomes the drawbacks of commonly used methods for measuring N₂ fixation by aquatic N‐fixers such as Azolla pinnata‐Anabaena azollae association (Azolla) is presented. The method was compared with ¹⁵N₂ gas (while maintaining CO₂) and the difference methods of measuring N₂ fixation. The isotopic dilution method was used for two conditions: a. For ¹⁵N‐free growth medium, Azolla was pre‐enriched with ¹⁵N, and N₂ fixation was determined by measuring the dilution of ¹⁵N in the tissue. b. For the growth medium containing N, N₂ fixation was determined by providing ¹⁵N enriched ammonium sulfate in the growth medium and measuring ¹⁵N to ¹⁴N ratio in the tissue. An airtight chamber, necessary for ¹⁵N₂ gas and acetylene reduction methods, was not representative of the growing environment of Azolla. Temperature in the airtight chamber was far from uniform and CO₂ was rapidly depleted. The isotopic dilution method is simpler, relatively inexpensive, subject to fewer errors and applicable to more diverse conditions, and yet was as accurate as ¹⁵N₂‐gas method.     

Nitrous oxide emissions and dynamics of soil nitrogen under 15N‐labeled cow urine and dung patches on a sandy grassland soil

Grazing animals highly influence the nutrient cycle by a direct return of 80% of the consumed N in form of dung and urine. In the autumn‐winter period, N uptake by the sward is low and rates of seepage water in sandy soils are high, hence high mineral‐N contents in soil and in seepage water as well as large losses of N₂O are expected after cattle grazing in autumn. The objective of this study was the quanitfication of N loss deriving from urine and dung leaching and by N₂O emission. Therefore the deposition of urine and dung patches was simulated in maximum rates excreted by cows by application of ¹⁵N‐labeled cow urine and dung (equivalent to 1030 kg N ha^–1 and 1052 kg N ha^–1, respectively) on a sandy pasture soil in N Germany. Leachate was collected in weekly intervals from free‐draining lysimeters, and ¹⁵N‐NO , ¹⁵N‐NH , and ¹⁵N‐DON (dissolved organic N) were monitored over 171 d. Furthermore, the ¹⁵N‐N₂O emission rates and the dynamics of inorganic ¹⁵N in the upper soil layer were monitored in a field trial, adjacent to the lysimeters. After 10 d following the urine application, the urea was completely hydrolyzed, shown by a 100% recovery of urine‐N in the soil NH . The following decrease of ¹⁵N‐NH in the soil was higher than the increase of ¹⁵N‐NO , and some N loss was explained by leaching. Amounts of 51% and 2.5% of the applied ¹⁵N were found in leachate as inorganic N, 2.4% and 0.7% as DON derived from urine and dung, respectively. Release of N₂O from urine and dung patches applied to the pasture was low, with losses of 0.05% and 0.33% of the applied ¹⁵N, respectively. Overall loss of dung‐derived N was very low, but as the bulk dung N remained in the soil, N loss after mineralization of the dung needs to be investigated.     

Variability of CO2 and N2O emissions during freeze‐thaw cycles: results of model experiments on undisturbed forest‐soil cores

The amounts of N₂O released in periods of alternate freezing and thawing depend on site and freezing conditions, and contribute considerably to the annual N₂O emissions. However, quantitative information on the N₂O emission level of forest soils in freeze‐thaw cycles is scarce, especially with regard to the direct and indirect effect of tree species and the duration of freezing. Our objectives were (i) to quantify the CO₂ and N₂O emissions of three soils under beech which differed in their texture, C and N contents, and humus types in freeze‐thaw cycles, and (ii) to study the effects of the tree species (beech (Fagus sylvatica L.) and spruce (Picea abies (L.) Karst.)) for silty soils from two adjacent sites and the duration of freezing (three and eleven days) on the emissions. Soils were adjusted to a matric potential of –0.5 kPa, and emissions were measured in 3‐hr intervals for 33 days. CO₂ emissions of all soils were similar in the two freeze‐thaw cycles, and followed the temperature course. In contrast, the N₂O emissions during thawing differed considerably. Large N₂O emissions were found on the loamy soil under beech (Loam‐beech) with a maximum N₂O emission of 1200 μg N m^–2 h^–1 and a cumulative emission of 0.15 g N m^–2 in the two thawing periods. However, the sandy soil under beech (Sand‐beech) emitted only 1 mg N₂O‐N m^–2 in the two thawing periods probably because of a low water‐filled pore space of 44 %. The N₂O emissions of the silty soil under beech (Silt‐beech) were small (9 mg N m^–2 in the two thawing periods) with a maximum emission of 150 μg N m^–2 h^–1 while insignificant N₂O emissions were found on the silty soil under spruce (0.2 mg N m^–2 in the two thawing periods). The cumulative N₂O emissions of the short freeze‐thaw cycles were 17 % (Sand‐beech) or 22 % (Loam‐beech, Silt‐beech) less than those of the long freeze‐thaw cycles, but the differences between the emissions of the two periods were not significant (P ≤ 0.05). The results of the study show that the amounts of N₂O emitted in freeze‐thaw cycles vary markedly among different forest soils and that the tree species influence the N₂O thawing emissions in forests considerably due to direct and indirect impacts on soil physical and chemical properties, soil structure, and properties of the humus layer.     

N2O emissions from an irrigated and non‐irrigated organic soil in eastern Canada as influenced by N fertilizer addition

Drainage and cultivation of organic soils often result in large nitrous oxide (N₂O) emissions. The objective of this study was to assess the impacts of nitrogen (N) fertilizer on N₂O emissions from a cultivated organic soil located south of Montréal, QC, Canada, drained in 1930 and used since then for vegetable production. Fluxes of N₂O were measured weekly from May 2004 to November 2005 when snow cover was absent in irrigated and non‐irrigated plots receiving 0, 100 or 150 kg N ha⁻¹ as NH₄NO₃. Soil mineral N content, gas concentrations, temperature, water table height and water content were also measured to help explain variations in N₂O emissions. Annual emissions during the experiment were large, ranging from 3.6 to 40.2 kg N₂O‐N ha⁻¹ year⁻¹. The N₂O emissions were decreased by N fertilizer addition in the non‐irrigated site but not in the irrigated site. The absence of a positive influence of soil mineral N content on N₂O emissions was probably in part because up to 571 kg N ha⁻¹ were mineralized during the snow‐free season. Emissions of N₂O were positively correlated to soil CO₂ emissions and to variables associated with the extent of soil aeration such as soil oxygen concentration, precipitation and soil water table height, thereby indicating that soil moisture/aeration and carbon bioavailability were the main controls of N₂O emission. The large N₂O emissions observed in this study indicate that drained cultivated organic soils in eastern Canada have a potential for N₂O‐N losses similar to, or greater than, organic soils located in northern Europe.