Denitrification characteristics of subtropical soils in China affected by soil parent material and land use

Forty‐five soil samples were collected from rice paddy land (R), tea garden land (T), forestland (F), brush land (B), and upland (U) in Jiangxi province, a subtropical region of China. These soils were derived from Quaternary red earth (Q), Tertiary red sandstone (S), and granite (G). Their denitrification capacities were determined after treatment with 200 mg NO₃⁻‐N kg⁻¹ soil by measuring changes in NO₃⁻‐N content during a 28‐day anaerobic incubation under N₂ gas in the headspace, at 30°C. The subtropical soils studied here were characterized by generally small denitrification capacities, ranging from no denitrification capacity to complete disappearance of added NO₃⁻‐N within 11 days of incubation. With few exceptions, NO₃⁻‐N reduction with incubation time followed a first‐order relationship with reaction constants of 0 – 0.271 day⁻¹, but the data could be simulated better by a logarithmic relationship. Thus, denitrification capacity was determined by the reaction constant of the first‐order reaction, the slope of the logarithmic relationship, and the averaged NO₃⁻‐N reduction rate in the first 7 days of anaerobic incubation (ranging from 0 to 28.5 mg kg⁻¹day⁻¹), and was significantly larger in the soils derived from G than from Q and S for all land uses except for rice paddy land. Soil organic carbon and nitrogen availability are the key factors that determine differences in denitrification capacity among the three soil parent materials. Rice cultivation significantly promoted denitrification capacity compared with the other four land uses and masked the effect of soil parent materials on denitrification capacity. This is most likely due to increases in organic carbon and total N content in the soil, which promoted the population and biological activities of microorganisms which are able to respire anaerobically when the rice soil is flooded. Neither the increased pH of upland soil caused by the addition of lime for upland crop production, nor the decreased pH of the tea garden soil by the acidification effect of tea plants altered soil denitrification capacity. Our results suggest that land use and management practices favour soil carbon and/or nitrogen accumulation and anaerobic microorganism activities enhance soil denitrification capacity.     

Nitrogen isotope discrimination in denitrification of nitrate in soils

Nitrogen isotope discrimination during denitrification in soils of nitrate containing natural concentrations of ¹⁴N and ¹⁵N was studied by determining the amount and the ¹⁵N content of nitrate-N and (nitrate + nitrite)-N in nitrate-treated soils incubated under anaerobic conditions (He atmosphere) for various times after treatment with glucose to promote denitrification. Analyses performed showed that the nitrate-N lost on incubation of these soils could largely be accounted for as products of denitrification (nitrite, NO. N₂O and N₂).The studies reported show that marked discrimination between ¹⁴N and ¹⁵N occurs during denitrification of nitrate in soils and that significant N isotope effects occur both in reduction of nitrate to nitrite and in reduction of nitrite to gaseous forms of N. They also indicate that the overall N isotope effect during denitrification of nitrate in soil will depend upon the tendency of the soil to accumulate nitrite under conditions that induce denitrification.It is concluded that discrimination between ¹⁴N and ¹⁵N during denitrification in soils of nitrate containing natural concentrations of these isotopes is of sufficient magnitude to invalidate the use of N isotope-ratio analyses for assessment of the contributions of soil and fertilizer N to nitrate in surface or ground waters or to nitrous oxide in the atmosphere.     

Pedotransfer functions for the pool size of slowly mineralizable organic N in sandy arable soils

The major aim of this study was to evaluate how the pool size of slowly mineralizable, ‘old’ soil organic N can be derived from more easily accessible soil and site information via pedotransfer functions (PTF). Besides modeling, this pool size might be of great importance for the identification of soils with high mineralization potential in drinking‐water catchments. From long‐term laboratory incubations (ca. 200 days) at 35 °C, the pool sizes of easily mineralizable organic N (N_fast), mainly in fresh residues, and slowly mineralizable, ‘old’ soil organic N (N_slow) as well as their first‐order rate coefficients were obtained. 90 sandy arable soils from NW Germany served to derive PTFs for N_slow that were evaluated using another 20 soils from the same region. Information on former land‐use and soil type was obtained from topographical, historical, and soil maps (partly from 1780). Pool size N_slow very strongly depends on soil type and former land‐use. Mean pool sizes of N_slow were much lower in old arable lowland (105 mg N kg^–1) than upland soils (175 mg N kg^–1) possibly due to lower clay contents. Within lowlands, mean pool sizes in former grassland soils (245 mg N kg^–1) were 2 to 3 times larger than in old arable soils due to accumulation of mineralizable N. In contrast, mean pool sizes of N_slow were lowest in recently cleared, former heath‐ and woodland (31 mg N kg^–1) as a result of the input of hardly decomposable organic matter. Neither N nor C in the light fraction (density < 1.8 g cm^–3) was adequate to derive pool size N_slow in the studied soils (r² < 0.03). Instead, N_slow can be accurately (r² = 0.55 – 0.83) derived from one or two basic soil characteristics (e.g. organic C, total N, C : N, mineral fraction < 20 μm), provided that sites were grouped by former land‐use. Field mineralization from N_slow during winter (independent data set) can be predicted as well on the basis of N_slow‐values calculated from PTFs that were derived after grouping the soils by former land‐use (r² = 0.51***). In contrast, using the PTF without soil grouping strongly reduced the reliability (r² = 0.16).     

Denitrification and total nitrogen gas production from forest soils of Eastern China

Reactive forms of nitrogen (Nr) are accumulating at local, regional and global levels largely due to human activities, particularly N-fertilizer production and use as well as fossil fuel combustion. This has resulted in a change in the nitrogen (N) cycle and excess Nr in the environment, which has negative environmental effects. Therefore, characterizing denitrification and the edaphic variables controlling denitrification and its products is the first step in predicting the long-term effects of Nr accumulation. In the present study, six forest soil types in different climatic zones were collected from East China and evaluated for denitrification products following a K¹⁵NO₃ amendment and subsequent incubation. The results showed that denitrification, indicated by production of nitric oxide (NO), nitrous oxide (N₂O) and dinitrogen (N₂), was higher in the studied temperate forest soils than in the studied subtropical and tropical forest soils and was negatively correlated with soil redox potential at the beginning of incubation (r = −0.94, P < 0.01), but not with soil pH. The ratios of NO/total N gas and N₂O/total N gas produced during denitrification varied among the soils, and were generally higher in the subtropical and tropical soils. Spearman's correlation analysis showed that the NO ratio was positively correlated with soil oxidation capacity (OXC) (r = 0.94, P < 0.01) and redox potential at the beginning of incubation (r = 0.86, P < 0.05), but negatively correlated with soil pH (r = −0.83, P < 0.05). The N₂O ratio was not significantly correlated with these edaphic variables, but showed a significant correlation to NO ratio (r = 0.83, P < 0.05). These results suggested that the OXC value might be the key factor affecting denitrification rates in soils. One possible explanation for these effects is that large OXC values would result in a higher level soil redox potential, thus suppressing denitrification and enhancing NO and N₂O ratios during denitrification.     

The effect of oxygen,pH and organic carbon on soil-layer specific denitrifying capacity in acid coniferous forest

Emissions of N₂O from acid coniferous forest soils are found to be low and considered to be due to nitrification rather than denitrification. Recently we have demonstrated soil-layer specific denitrification in a Scots pine forest in the Netherlands. N₂O production, in the presence of high concentrations of acetylene, was detected in the intact needle fraction but was absent in the fragmentation layer of this forest soil. To identify the factors regulating denitrification activity, in the present study the effects of oxygen, pH and organic carbon were investigated in the needle and fragmentation fraction of acid coniferous forest soils. Under natural circumstances denitrification in the Scots pine needles was higher than in Douglas fir needles and absent in fragmentation material. Under anaerobic conditions comparable N₂O production in the two soil types was found in needle suspensions of both forest types, indicating that differences in anaerobic microsites were responsible for different N₂O production under aerobic circumstances. Denitrifying capacity was absent in the fragmentation layer; under anaerobic circumstances little N₂O was produced. Neither an addition of available carbon (glucose and succinate) nor an increase in pH revealed a denitrifying capacity comparable to that observed in needles. The increase in pH, under anaerobic circumstances, was most effective on N₂O production in the fragmentation material. The denitrifying capacity in the fragmentation layer remained low during short-term incubation under optimal conditions. This indicates the presence of a low denitrifying population, most likely due to aerobic conditions, low pH and low available organic carbon. Although the significance of N₂O production under natural conditions remains speculative, this study seeks to clarify soil-layer specific denitrifying activity in acid coniferous forest soils.     

Organic matter availability for denitrification in soils of different textures and drainage classes

Abstract

Soils from the A, B, and C horizons representing three natural drainage classes and differing textures were chosen to study relationships between denitrification rate and estimates of available carbon. The highest correlation with denitrification rate was obtained with total organic C. Water‐extractable C, mineralizable C and 0.1 N Ba(OH)2‐extractable C produced less satisfactory correlations. When soils of the B and C horizons only were included in the regression analysis, 0.1 N Ba(OH)₂‐extractable C was found to be unsatisfactory as a predictor of available C for soil denitrifiers. None of the four methods for estimating available C were found adequate for B and C horizon soils which were relatively low in available C. Coarser‐textured soils with relatively low C levels had correspondingly low denitrification rates. Regressions of denitrification rate on mineralizable C or water‐extractable C were nonsignificant with poorly drained soils whereas they were highly significant with well or imperfectly drained soils.     

围海造田长期耕种稻田和旱地土壤氮矿化速率及供氮潜力比较

围海造田是沿海地区拓展土地面积的主要途径。土壤氮矿化参数是揭示围海造田土壤肥力演变和土壤氮供应的重要指标,但是我国沿海造田土壤的相关研究少有报道。本研究以杭州湾南岸海积平原上慈溪市1000年和520年筑塘造田区为对象,选择4个代表性采样点,每个点从低洼稻田采集1个表层混合水稻土,在其相邻高地采集1个表层混合旱地土壤,共8个样品。采用间隙淋洗法研究了土壤样品氮矿化动力学特征。结果如下: 119 d培养试验证实水稻土和旱地土壤有机氮矿化动力学符合一级反应动力学方程Nt=N0(1-e-kt); 水稻土有机氮矿化势（N0）为82.7～161.9 mg/kg（平均114 mg/kg）,占有机氮的7.3%,旱地土壤N0为63.9～104.4 mg/kg（平均83.4 mg/kg）,占有机氮的7.3%; 水稻土有机氮矿化速率（k）为0.033～0.114/d（平均0.064/d）,旱地土壤k为0.007～0.023/d（平均0.020/d）。土壤综合供氮指标（N0k）,水稻土为3.8418.46 mg/(kgd)［平均8.0 mg/(kgd)］,旱地土壤为0.54～2.66 mg/(kgd)［平均1.6 mg/(kgd)］。水稻土总氮含量为1.4～2.0 g/kg （平均1.6 g/kg）,旱地为0.87～2.0 g/kg（平均1.3 g/kg）。可见,水稻土氮库、供氮潜力和速率均大于相邻旱地土壤。因此,从土壤氮肥力来讲,相对于旱地,围海形成的水稻田更具有可持续利用性。     

Production and consumption of N2O during denitrification in subtropical soils of China

Purpose

Nitrous oxide (N₂O) production and reduction rates are dependent on the interactions with each other and it is therefore important to evaluate them within the context of simultaneously operating N₂O emission and reduction. The objective of this study was to quantify the simultaneously occurring N₂O emission and reduction across a range of subtropical soils in China, to gain a mechanistic understanding of potential N₂O dynamics under the denitrification condition and their important drivers, and to evaluate the potential role of the subtropical soils as either sources or sinks of N₂O through denitrification.

Materials and methods

Soils (45, from a range of different land uses and soil parent materials) were collected from the subtropical region of Jiangxi Province, China, and tested for their potential capacity for N₂O emission and N₂O reduction to N₂ during denitrification. N₂O emission and reduction were determined in a closed system under N₂ headspace after the soils were treated with 200?mg?kg^?1 NO ₃ ^? -N and incubation at 30?°C for 28?days. The soil physical and chemical properties, the temporal variations in headspace N₂O concentration, and NO ₃ ^? -N and NH ₄ ⁺ -N concentrations in the soil slurry were measured.

Results and discussion

Variations in N₂O concentration (N) over incubation time (t) were consistent with an equation in which average R ²?=?0.84?±?0.11 (p?<?0.05): $ N = A \times \left( {1 - \exp \left( { - {k_1} \times t} \right)} \right) - B \times \exp \left( {{k_2} \times t} \right) $ , where A is the total N₂O emission during the incubation, B is a constant, and k ₁ and k ₂ are the N₂O emission constant and reduction constants, respectively. The results of the simulation showed that k ₁ was greater than k ₂. The reduced amount of NO ₃ ^? -N in the first 7?days of incubation and the N₂O emission rate (the percentage of A value relative to the amount of NO ₃ ^? -N reduced during the 28-day incubation, R _n) were able to explain 82.9?% (p?<?0.01) of the variation in total N₂O emission (A) during the incubation for the soil samples studied, indicating that the total amount of N₂O emitted was determined predominately by denitrification capacity. Soil organic carbon content and soil nitrogen mineralization are the key factors that determine differences in the amounts of reduced NO ₃ ^? -N among the soil samples. The R _n value decreased with increasing k ₂ (p?<?0.01), indicating that soils with higher N₂O reduction capacity under these incubation conditions would emit less N₂O per unit of denitrified NO ₃ ^? -N than the other soils. Results are valuable in the evaluation of net N₂O emissions in the subtropical soils and the global N budget.

Conclusions

In a closed, anaerobic system, variations in N₂O concentration in the headspace over the incubation time were found to be compatible with a nonlinear equation. Soil organic carbon and the amount of NH ₄ ⁺ -N mineralized from the organic N during the first 7?days of incubation are the key factors that determine differences in the N₂O emission constant (k ₁), the N₂O reduction constant (k ₂), the total N₂O emission during the incubation (A) and the N₂O emission rate (R _n).     

Estimation of the total gaseous nitrogen losses from clay soils under laboratory and field conditions

Acetylene blockage was evaluated as a method for measuring losses of N₂O + N₂ from two Denchworth series clay soils. The denitrification potential in anaerobic, dark incubations at 20°C with nitrate (equivalent to 100 kg N ha^?1 0–20 cm depth), maximum water holding capacity, and acetylene (1%), was equivalent to 32 ± 11 and 39 ± 6 kg N ha^?1 per day for the two 0–20 cm soils and was positively correlated with carbon content (r= 0.98). After 4 days N₂O was reduced to N₂ in the presence of C₂H₂. In April 1980 following irrigation (24 mm) and applications of ammonium nitrate (70 kg N ha^?1) and acetylene, the mean nitrous oxide flux from soil under permanent grass was 0.05 ± 0.01 kg N₂O-N ha^?1 per day for 8 days. In June 1980, the losses of nitrogen from cultivated soils under winter wheat after irrigation (36 mm) and acetylene treatment were 0.006 ± 0.002 and 0.04–0.07 ± 0.01 kg N ha^?1 per day respectively before and after fertilizer application (70 kg N ha^?1). The nitrous oxide flux in the presence of acetylene decreased briefly, indicating that nitrification was rate determining in drying soil.     

Effect of Rice Residues on Carbon Dioxide and Nitrous Oxide Emissions from a Paddy Soil of Subtropical China

A pot incubation experiment with rice residues (straw and root) was conducted under aerobic condition (60% of WHC, water holding capacity) for a period of 55 days in a greenhouse. The emissions of carbon dioxide (CO₂) and nitrous oxide (N₂O) were determined by the closed chamber method in a paddy soil. The soil was derived from quaternary red clay, and collected from the Ecological Station of Red Soil, the Chinese Academy of Sciences, located in Jiangxi Province, a subtropical region of China. The emissions of CO₂ and N₂O were increased by the amendment of rice residues. Significantly positive correlation was found between N₂O and CO₂ fluxes (R = 0.650*?0.870*, P ≤ 0.05). The cumulative emissions during the early stage of the incubation (<25 days after residue addition) accounted for about 67%–86% and 67%–80% of the total amount of CO₂ and N₂O emissions, respectively. Cumulative emissions and emission factors of the two gases were higher in the soils amended with rice straw than those with rice root. The two gas fluxes were positively correlated with microbial biomass C and N, as well as soluble organic C. N₂O flux was positively correlated with NH₄ ⁺–N content at the early stage (<25 days), and negatively with NO₃ ^?–N content at the later stage of this incubation (25–55 days), implying that both nitrification and denitrification may have contributed to N₂O production.     

Microbial activities in a histosol: Effects of wood ash and NPK fertilizers

Mineralization of organic matter and microbial activities in an intensively cultivated acid, N-rich peat soil planted with Salix sp. cv. aquatica were examined for 3 yr. The soil was amended with wood ash or NPK fertilizers providing N as ammonium nitrate or urea. The wood ash amendment (10 tons ha^?1) increased soil pH from 4.6 to 5.5 and increased markedly all microbial activities measured, resulting in increased mineralization and N availability, and in loss of 9% total soil N during the first year. The addition of ammonium nitrate caused a corresponding though less pronounced increase in N mineralization. Cellulose decomposition increased in all amended soils, reaching rates 53–86% higher than in non-amended soil. Potential N₂ fixation (C₂H₂ reduction) by free-living organisms was increased by the ash-amendment. Potential denitrification rates were positively correlated (r = 0.98) with the presence of water-soluble organic-C, which was more abundant in ash-amended and non-amended soils than in the soils fertilized with N.     

Denitrification losses from puddled rice soils in the tropics

Summary Although denitrification has long been considered a major loss mechanism for N fertilizer applied to lowland rice (Oryza sativa L.) soils, direct field measurements of denitrification losses from puddled rice soils in the tropics have only been made recently. This paper summarizes the results of direct measurement and indirect estimation of denitrification losses from puddled rice fields and reviews the status of research methodology for measurement of denitrification in rice fields. The direct recovery of (N₂+N₂O)-¹⁵N from ¹⁵N-enriched urea has recently been measured at sites in the Philippines, Thailand, and Indonesia. In all 12 studies, recoveries of (N₂+N₂O)-¹⁵N ranged from less than 0.1 to 2.2% of the applied N. Total gaseous N losses, estimated by the ¹⁵N-balance technique, were much greater, ranging from 10 to 56% of the applied urea-N. Denitrification was limited by the nitrate supply rather than by available C, as indicated by the values for water-soluble soil organic C, floodwater (nitrate+nitrite)-N, and evolved (N₂+N₂O)-¹⁵N from added nitrate. In the absence of runoff and leaching losses, the amount of (N₂+N₂O)-¹⁵N evolved from ¹⁵N-labeled nitrate was consistently less than the unrecovered ¹⁵N in ¹⁵N balances with labeled nitrate, which presumably represented total denitrification losses. This finding indicates that the measured recoveries of (N₂+N₂O)-¹⁵N had underestimated the denitrification losses from urea. Even with a probable two-or threefold underestimation, direct measurements of (N₂+N₂O)-¹⁵N failed to confirm the appreciable denitrification losses often estimated by the indirect difference method. This method, which determines denitrification losses by the difference between total ¹⁵N loss and determined ammonia loss, is prone to high variability. Measurements of nitrate disappearance and ¹⁵N-balance studies suggest that nitrification-denitrification occurs under alternate soil drying and wetting conditions both during the rice cropping period and between rice crops. Research is needed to determine the magnitude of denitrification losses when soils are flooded and puddled for production of rice.     

Boiling Potassium Chloride–Extractable Nitrogen as an Index of Potentially Mineralizable and Plant‐Available Nitrogen in Soil

Abstract

Mineralization of soil organic nitrogen (N) and its contribution toward crop N uptake is central to developing efficient N‐management practices. Because biological incubation methods are time consuming and do not fit into the batch‐analysis techniques of soil‐testing laboratories, an analytical procedure that can provide an estimate of the mineralizable N would be useful as a soil‐test method for predicting plant‐available N in soil. In the present studies, the ability of boiling potassium chloride (KCl) to extract potentially mineralizable and plant‐available N in arable soils of semi‐arid India was tested against results from biological incubations and uptake of N by wheat in a pot experiment. Mineralization of organic N in soils was studied in the laboratory by conducting aerobic incubations for 112 days at 32°C and 33 KPa of moisture. Cumulative N mineralization in different soils ranged from 8.2 to 75.6 mg N kg^?1 soil that constituted 2.7 to 8.8% of organic N. The amount of mineral N extracted by KCl increased with increase in length of boiling from 0.5 to 2 h. Boiling for 0.5, 1, 1.5, and 2 h resulted in an increase in mineral‐N extraction by 9.3, 12.7, 19.6, and 26.1%, respectively, as compared to mineral N extracted at room temperature. The boiling‐KCl‐hydrolyzable N (ΔN_i) was directly dependent upon soil organic N content, but the presence of clay retarded hydrolysis for boiling lengths of 0.5 and 1 h. However, for boiling lengths of 1.5, and 2 h, the negative effect of clay was not apparent. The ΔN _i was significantly (P=0.05) correlated to cumulative N mineralized and N‐mineralization potential (N₀). The relationship between N₀ and ΔN _i was curvilinear and was best described by a power function. Boiling length of 2 h accounted for 78% of the variability in N₀. Results of the pot experiment showed that at 21‐ and 63‐day growth stages, dry‐matter yield and N uptake by wheat were significantly correlated to boiling‐KCl‐extractable mineral N. Thus, boiling KCl could be used to predict potentially mineralizable and plant‐available N in these soils, and a boiling time of 2 h was most suitable to avoid the negatively affected estimates of boiling‐KCl‐hydrolyzable N in the presence of clay. The results have implications for selecting length of boiling in soils varying widely in clay content, and this may explain why, in earlier studies, longer boiling times (viz. 2 or 4 h) were better predictors of N availability as compared to 0.5 and 1 h.     

Denitrification potentials: Measurement of seasonal variation using a short-term anaerobic incubation technique

A short-term anaerobic incubation technique using the C₂H₂ inhibition of N₂O-reductase for comparing denitrification potentials of soils is described. Twenty grams of soil with added NO^?1₃ are incubated in the presence of He and 0.1 atm C₂H₂ at 25°C and 0 soil matric potential for 8 h. N₂O evolution is linear within 60 to 120 min. The denitrification potential of soils stored at 4°C decreased markedly over 21 days of storage in accordance with changes in the available C. Denitrification under an anaerobic atmosphere was observed at 4 C. Denitrification potentials were independent of NO^?3₃ concentrations above 25 μg NO^?₃-N g^?1 soil. Biphasic linear rates of N₂O evolution were observed in one soil. Incubation of this soil with chloramphenicol suggested the first linear phase is attributable to the in situ enzyme activity at the time of sampling. The second linear phase is indicative of the dentrification potential and is attributed to the full induction of denitrifying enzymes. The denitrification potential of a soil was maintained at or close to the maximum for 8 months of the year. During midsummer months the denitrification potential decreased markedly and the soil demonstrated a biphasic rate of denitrification suggesting an in situ denitrification activity less than the maximum potential. Results indicate that the maximum denitrification potential of this soil may often be limited not by NO^?₃ but by available C.     

Arylamidase Activity as an Index of Nitrogen Mineralization in Soils

Abstract

The enzyme arylamidase [EC 3.4.11.2] catalyzes the hydrolysis of N‐terminal amino acids from arylamides. Because it has been proposed that this enzyme may play a major role in nitrogen (N) mineralization in soils, studies were carried out using short‐term laboratory incubations under aerobic and anaerobic conditions and chemical hydrolysis of soil organic N to assess the N mineralization in a range of 51 soils from six agroecological zones of the North Central region of the United States. The enzyme activity was assayed at its optimal pH value. With the exception of the values obtained for field‐moist soils incubated under anaerobic conditions, the amounts of N mineralized by all the biological and chemical methods studied were significantly correlated with arylamidase activity, with r values of 0.54*** for the amounts of inorganic N produced under aerobic incubation, of 0.44** for anaerobic incubation of air‐dried soils, of 0.53*** and 0.55*** for the amounts of ammonium (NH₄ ⁺)‐N released by steam distillation with PO₄‐B₄O₇ for 4 and 8 min, respectively; and of 0.49*** and 0.53*** for the amounts of NH₄ ⁺‐N released by steam distillation with disodium tetraborate (Na₂B₄O₇) for 4 min or 8 min, respectively. The amounts of N extractable with hot potassium chloride (KCl) were most significantly correlated with arylamidase activity (r=0.56***). Arylamidase activity was significantly correlated with organic carbon (C) (r=0.49***), organic N (r=0.55***), and fixed ammonium (NH₄ ⁺)‐N (r =0.42**).     

Einfluß einer hohen Nitratdüngung auf Kinetik und Gaszusammensetzung der Denitrifikation in unterschiedlichen Böden

Effect of high nitrate application on the kinetic and gaseous composition of denitrification in different soils Kinetic and gaseous composition of denitrification were studied with 16 different soil horizons after application of a relatively high amount of nitrate (400 μg NO N/g dry soil) at defined conditions (He atmosphere; 80 % WHC; 30°C; 3 weeks). At the conditions given, denitrification followed zero-order kinetics depending on the amount of decomposable organic matter rather on than the nitrate concentration. Denitrification intensity was most significantly correlated with the amount of extractable or mineralizable organic carbon (C_H2O and C_min, respectively). N₂ and N₂O (but not NO) were liberated by all samples, the amount and ratio depending on the soil and time of sampling. At the end of the three week's incubation period, the N₂/N-N₂O ratio varied between 8.1 and 1.4/1 (with an average of 3.1/1), except for the acid Ah-sample of the Pararendzina (N₂/N-N₂O = 1.0/1.2). The incorporation of an excess of easily decomposable leaf-powder resulted in an increased nitrate turn-over (from 64.7 % to 95,7 % of the nitrate loss) with N₂ as the single denitrification product. N₂O could be detected only with the acid “B”-material of the Pararendzina. The denitrifying capacity Y (in μg N₂+N-N₂O/g soil) of a soil at the conditions given may be predicted by the amount of water-extractable organic carbon X (in μg C_H2O/g soil) according to the equation Y = 0.808 X + 120,1.     

Nitrate enhances N2O emission more than ammonium in a highly acidic soil

Purpose

Nitrous oxide (N₂O) is produced naturally in soils through microbial processes of nitrification and denitrification. In recent years, the long-term application of nitrogen-heavy fertilizers has led to the acidification of tea orchard soils with high N₂O emission. The present research aimed at finding out which process (nitrification or denitrification) dominates in N₂O production, whether certain fertilizer managements could reduce N₂O emission, and the effects of fertilizer management on the abundance of functional genes.

Materials and methods

Two nitrification inhibitors, 3, 4-dimethylpyrazole phosphate (DMPP) and dicyandiamide (DCD), combined with different N fertilizers (ammonium sulfate and potassium nitrate) were applied to highly acidic tea orchard soil in an aerobic incubation experiment. Both amoA and nosZ gene abundances from different treatments were determined by quantitative PCR. An anaerobic nitrate effect test was carried out using C₂H₂ inhibition method.

Results and discussion

The application of nitrate fertilizers significantly (P?<?0.05) enhanced total N₂O emission. A linear regression analysis between total N₂O emission and average nitrate contents indicated that denitrification is the dominant source of N₂O in this tea orchard soil. In the anaerobic incubation, no significant difference of N₂O emission was observed between KNO₃ and no KNO₃ treatments before 96 h. Quantitative PCR revealed lower copy numbers of nosZ in nitrate-associated fertilizer-treated soils than the soils from other treatments. Compared with the control, ammonium fertilizers with DCD or DMPP significantly (P?<?0.05) inhibited nitrate production as well as N₂O.

Conclusions

These results showed that denitrification is the dominant source of N₂O in this highly acidic soil. Nitrate addition could significantly inhibit the abundance of nitrous oxide reductase, therefore causing high N₂O emission. The application of ammonium fertilizers with DCD or DMPP could significantly reduce N₂O emission, possibly due to the effective inhibition of nitrate production.     

Phases of denitrification following oxygen depletion in soil

The short-term response of soil denitrification to reduced aeration was studied using the acetylene inhibition method for the assay of denitrification. Two distinct phases of denitrification rate were observed. An initial constant rate, termed phase I, was not decreased by chloramphenicol, was increased slightly or not at all by organic carbon amendment, and lasted for 1–3 h. Phase I was attributed to the activity of pre-existing denitrifying enzymes in the soil microflora. Following phase I the denitrification rate increased; chloramphenicol inhibited this increase. In soils without organic-C amendment a second linear phase, termed phase II, was attained after 4–8 h of anaerobic incubation. The linearity of this phase was attributed to the full derepression of denitrifying enzyme synthesis by the indigenous population and to the lack of significant growth of denitrifiers. Phase I rate was dependent on the initial or in situ aeration state of the soil sample; phase II was not. Therefore, phase I may be more directly related to field denitrification rates.Denitrification rate changes following water saturation of soils in aerobic atmospheres were also examined. Rates were greatly increased by wetting but only after a lag of several hours. Our interpretation is that following wetting of natural soils, anaerobic or partially anaerobic conditions are established by respiration and reduced O₂ diffusion rate; this first eliminates O₂ inhibition then derepresses the synthesis of denitrifying enzymes. Although denitrifying enzymes are apparently present even in relatively dry soils, their activity is low until O₂ inhibition is eliminated. From this evidence we reason that most N is lost from soils during brief periods beginning a few hours after irrigation or a rainfall.     

Nitrous oxide fluxes and denitrification sensitivity to temperature in Irish pasture soils

Nitrous oxide (N₂O) emissions from grazed pastures constitute approximately 28% of total global anthropogenic N₂O emissions. The aims of this study were to investigate the effect of inorganic N fertilizer application on fluxes of N₂O, quantify the emission factors (EFs) for a sandy loam soil which is typical of large areas in Ireland and to investigate denitrification sensitivity to temperature. Nitrous oxide flux measurements from a cut and grazed pasture field for 1 year and denitrification laboratory incubation were carried out. The soil pH was 7.3 and had a mean organic C and N content at 0–20 cm of 44.1 and 4.4 g/kg dry weight, respectively. The highest observed peaks of N₂O fluxes of 67 and 38.7 g N₂O‐N per hectare per day were associated with times of application of inorganic N fertilizer. Annual fluxes of N₂O from control and fertilized treatments were 1 and 2.4 kg N₂O‐N per hectare, respectively. Approximately 63% of the annual flux was associated with N fertilizer application. Multiple regression analysis revealed that soil nitrate and the interaction between soil nitrate and soil water content were the main factors controlling N₂O flux from the soil. The derived EF of 0.83% was approximately 66% of the IPCC default EF value of 1.25% as used by the Irish EPA to estimate greenhouse gases (GHGs) in Ireland. The IPCC‐revised EF value is 0.9%. A highly significant exponential regression (r² = 0.98) was found between denitrification and incubation temperature. The calculated Q₁₀ ranged from 4.4 to 6.2 for a temperature range of 10–25 °C and the activation energy was 47 kJ/mol. Our results show that denitrification is very sensitive to increasing temperature, suggesting that future global warming could lead to a significant increase in soil denitrification and consequently N₂O fluxes from soils.     

Microbial pathways for nitrous oxide emissions from sheep urine and dung in a typical steppe grassland

The aim of this study was to determine the responses of nitrifiers and denitrifiers to understand microbial pathways of nitrous oxide (N₂O) emissions in grassland soils that received inputs of sheep excreta. Sheep dung and synthetic sheep urine were applied at three different rates, simulating a single, double, or triple overlapping of urine or dung depositions in the field. Quantitative PCR and high-throughput sequencing were combined with process-based modeling to understand effects of sheep excreta on microbial populations and on pathways for N₂O production. Results showed that emissions of N₂O from urine were significantly higher than from dung, ranging from 0.12 to 0.78 kg N₂O-N ha^?1 during the 3 months. The N₂O emissions were significantly related to the bacterial amoA (r?=?0.373, P?<?0.001) and nirK (r?=?0.614, P?<?0.001) gene abundances. It was autotrophic nitrification that dominated N₂O production in the low urine-N rate soils, whereas it was denitrification (including nitrifier denitrification and heterotrophic denitrification) that dominated N₂O production in the high urine-N rate soils. Nitrifier denitrification was responsible for most of the N₂O emissions in the dung-treated soils. This study suggests that nitrifier denitrification is indeed an important pathway for N₂O emissions in these low fertility and dry grazed grassland ecosystems.