N2O emissions and product ratios of nitrification and denitrification as affected by freezing and thawing

Agricultural soils contribute significantly to atmospheric nitrous oxide (N₂O). A considerable part of the annual N₂O emission may occur during the cold season, possibly supported by high product ratios in denitrification (N₂O/(N₂+N₂O)) and nitrification (N₂O-N/(NO₃⁻-N+NO₂⁻-N)) at low temperatures and/or in response to freeze-thaw perturbation. Water-soluble organic materials released from frost-sensitive catch crops and green manure may further increase winter emissions. We conducted short-term laboratory incubations under standardized moisture and oxygen (O₂) conditions, using nitrogen (N) tracers (¹⁵N) to determine process rates and sources of emitted N₂O after freeze-thaw treatment of soil or after addition of freeze-thaw extract from clover. Soil respiration and N₂O production was stimulated by freeze-thaw or addition of plant extract. The N₂O emission response was inversely related to O₂ concentration, indicating denitrification as the quantitatively prevailing process. Denitrification product ratios in the two studied soils (pH 4.5 and 7.0) remained largely unaltered by freeze-thaw or freeze-thaw-released plant material, refuting the hypothesis that high winter emissions are due to frost damage of N₂O reductase activity. Nitrification rates estimated by nitrate (NO₃⁻) pool enrichment were 1.5-1.8 μg NO₃-N g⁻¹ dw soil d⁻¹ in freeze-thaw-treated soil when incubated at O₂ concentrations above 2.3 vol% and one order of magnitude lower at 0.8 vol% O₂. Thus, the experiments captured a situation with severely O₂-limited nitrification. As expected, the O₂ stress at 0.8 vol% resulted in a high nitrification product ratio (0.3 g g⁻¹). Despite this high product ratio, only 4.4% of the measured N₂O accumulation originated from nitrification, reaffirming that denitrification was the main N₂O source at the various tested O₂ concentrations in freeze-thaw-affected soil. N₂O emission response to both freeze-thaw and plant extract addition appeared strongly linked to stimulation of carbon (C) respiration, suggesting that freeze-thaw-induced release of decomposable organic C was the major driving force for N₂O emissions in our soils, both by fuelling denitrifiers and by depleting O₂. The soluble C (applied as plant extract) necessary to induce a CO₂ and N₂O production rate comparable with that of freeze-thaw was 20-30 μg C g⁻¹ soil dw. This is in the range of estimates for over-winter soluble C loss from catch crops and green manure plots reported in the literature. Thus, freeze-thaw-released organic C from plants may play a significant role in freeze-thaw-related N₂O emissions.     

Compaction effects on CO2 and N2O production during drying and rewetting of soil

The effects of compaction on soil porosity and soil water relations are likely to influence substrate availability and microbial activity under fluctuating soil moisture conditions. We conducted a short laboratory incubation to investigate the effects of soil compaction on substrate availability and biogenic gas (CO₂ and N₂O) production during the drying and rewetting of a fine-loamy soil. Prior to initiating the drying and wetting treatments, CO₂ production (−10 kPa soil water content) from uncompacted soil was 2.3 times that of compacted soil and corresponded with higher concentrations of microbial biomass C (MBC) and dissolved organic C (DOC). In contrast, N₂O production was 67 times higher in compacted than uncompacted soil at field capacity. Soil aeration rather than substrate availability (e.g. NO₃⁻ and DOC) appeared to be the most important factor affecting N₂O production during this phase. The drying of compacted soil resulted in an initial increase in CO₂ production and a nearly two-fold higher average rate of C mineralization at maximum dryness (owing to a higher water-filled pore space [WFPS]) compared to uncompacted soil. During the drying phase, N₂O production was markedly reduced (by 93-96%) in both soils, though total N₂O production remained slightly higher in compacted than uncompacted soil. The increase in CO₂ production during the first 24 h following rewetting of dry soil was about 2.5 times higher in uncompacted soil and corresponded with a much greater release of DOC than in compacted soil. MBC appeared to be the source of the DOC released from uncompacted soil but not from compacted soil. The production of N₂O during the first 24 h following rewetting of dry soil was nearly 20 times higher in compacted than uncompacted soil. Our results suggest that N₂O production from compacted soil was primarily the result of denitrification, which was limited by substrates (especially NO₃⁻) made available during drying and rewetting and occurred rapidly after the onset of anoxic conditions during the rewetting phase. In contrast, N₂O production from uncompacted soil appeared to be primarily the product of nitrification that was largely associated with an accumulation of NO₃⁻ following rewetting of dry soil. Irrespective of compaction, the response to drying and rewetting was greater for N₂O production than for CO₂ production.     

Soil carbon dioxide flux, carbon sequestration and crop productivity in a tropical dryland agroecosystem: Influence of organic inputs of varying resource quality

In view of the significance of agricultural soils in affecting global C balance, the impact of manipulation of the quality of exogenous inputs on soil CO₂–C flux was studied in rice–barley annual rotation tropical dryland agroecosystem. Chemical fertilizer, Sesbania shoot (high quality resources), wheat straw (low quality resource) and Sesbania + wheat straw (high + low quality), all carrying equivalent recommended dose of N, were added to soil. A distinct seasonal variation in CO₂–C flux was recorded in all treatments, flux being higher during rice period, and much reduced during barley and summer fallow periods. During rice period the mean CO₂–C flux was greater in wheat straw (161% increase over control) and Sesbania + wheat straw (+129%) treatments; however, during barley and summer fallow periods differences among treatments were small. CO₂–C flux was more influenced by seasonal variations in water-filled pore space compared to soil temperature. In contrast, the role of microbial biomass and live crop roots in regulating soil CO₂–C flux was highly limited. Wheat straw input showed smaller microbial biomass with a tendency of rapid turnover rate resulting in highest cumulative CO₂–C flux. The Sesbania input exhibited larger microbial biomass with slower turnover rate, leading to lower cumulative CO₂–C flux. Addition of Sesbania to wheat straw showed higher cumulative CO₂–C flux yet supported highest microbial biomass with lowest turnover rate indicating stabilization of microbial biomass. Although single application of wheat straw or Sesbania showed comparable net change in soil C (18% and 15% relative to control, respectively) and crop productivity (32% and 38%), yet they differed significantly in soil C balance (374 and −3 g C m⁻² y⁻¹ respectively), a response influenced by the recalcitrant and labile nature of the inputs. Combining the two inputs resulted in significant increment in net change in soil C (33% over control) and crop yield (49%) in addition to high C balance (152 g C m⁻² y⁻¹). It is suggested that appropriate mixing of high and low quality inputs may contribute to improved crop productivity and soil fertility in terms of soil C sequestration.     

Denitrification,N2-fixation and fermentation during anaerobic incubation of soils amended with glucose and nitrate

Nitrate and glucose additions were investigated for their role in the C and N dynamics during anaerobic incubation of soil. A gas-flow soil core method was used, in which the net production of N₂, N₂O, NO, CO₂, and CH₄ under a He atmosphere could be monitored both accurately and frequently. In all experiments clayey silt loam soil samples were incubated for 9 days at 25 °C. Addition of nitrate (50 mg KNO₃-N kg^-1 soil) had no effect on total denitrification and CO₂ production rates, while the N₂O/N₂ ratio was affected considerably. The cumulative N₂O production exceeded the cumulative N₂ production for 6 days in the treatment with nitrate addition, compared to 1.2 days in the unamended treatment. Glucose addition stimulated the microbial activity considerably. The denitrification rates were limited by the growth rate of the denitrifying population. During denitrification no significant differences were observed between the treatments with 700 mg glucose-C kg^-1 and 4200 mg glucose-C kg^-1, both in combination with 50 mg KNO₃-N kg^-1. The N₂ production rates were remarkably low, until NO _inf3 ^sup- exhaustion caused rapid reduction of N₂O to N₂ at day 2. During the denitrification period 15–18 mg N kg^-1 was immobilised in the growing biomass. After NO _inf3 ^sup- shortage, a second microbial population, capable of N₂-fixation, became increasingly important. This change was clearly reflected in the CO₂ production rates. Net volatile fatty acid (VFA) production was monitored during the net N₂-fixation period with acetate as the dominant product. N₂-fixation faded out, probably due to N₂ shortage, followed by increased VFA production. In the high C treatment butyrate became the most important VFA, while in the low C treatment acetate and butyrate were produced at equal rates. During denitrification no VFA accumulation occurred; this does not prove, however, that denitrification and fermentation appeared sequentially. The experiments illustrate clearly the interactions of C-availability, microbial population and nitrate availability as influencing factors on denitrification and fermentation.Dedicated to Professor J. C. G. Ottow on the occasion of his 60th birthday     

Influence of Biochar Addition on the Denitrification Process and N<Subscript>2</Subscript>O Emission in Cd-Contaminated Soil

The aim of this study was to investigate the effect of biochar addition on the denitrification process and N₂O emission in Cd-contaminated soil. Four different biochars, i.e., dairy manure and rice straw pyrolyzed at 350 and 550 °C, respectively, were added into a Cd-contaminated soil and incubation experiments were conducted for 8 weeks. Results showed that Cd had an inhibitory effect on denitrifying reductase enzymes and reduced the abundance of functional genes. On the contrary, amendment with the biochars increased denitrifying enzyme activity and gene abundance, and thus, enhanced the denitrification process. Labile carbon (C) in the biochar-amended soil, which was calculated based on the two-pool exponential model, was the key factor to facilitate this process. As a less important factor, elevated soil pH by biochar addition also increased denitrifying activity as well as the nosZ abundance. Decrease of Cd bioavailability by the biochar addition was beneficial to the denitrification process. Addition of the biochars with higher amount of NO₃ ^?-N, especially the rice straw-derived biochars, increased cumulative N₂O emission by more than ten times relative to the Cd-contaminated soil. With the great amount of labile C and NO₃ ^?-N, the treatment of biochars prepared at 350 °C released the larger amount of CO₂ and N₂O than other treatments. The biochar addition could totally release the heavy metal stress and restore the Cd-contaminated soil in terms of bacterial community.     

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.     

Linkage of N2O emissions to the abundance of soil ammonia oxidizers and denitrifiers in purple soil under long-term fertilization

Abstract

Microbial nitrification and denitrification are responsible for the majority of soil nitrous (N₂O) emissions. In this study, N₂O emissions were measured and the abundance of ammonium oxidizers and denitrifiers were quantified in purple soil in a long-term fertilization experiment to explore their relationships. The average N₂O fluxes and abundance of the amoAgene in ammonia-oxidizing bacteria during the observed dry season were highest when treated with mixed nitrogen, phosphorus and potassium fertilizer (NPK) and a single N treatment (N) using NH₄HCO₃as the sole N source; lower values were obtained using organic manure with pig slurry and added NPK at a ratio of 40%:60% (OMNPK),organic manure with pig slurry (OM) and returning crop straw residue plus synthetic NH₄HCO₃fertilizer at a ratio of 15%:85% (SRNPK). The lowest N₂O fluxes were observed in the treatment that used crop straw residue(SR) and in the control with no fertilizer (CK). Soil NH₄⁺provides the substrate for nitrification generating N₂O as a byproduct. The N₂O flux was significantly correlated with the abundance of the amoA gene in ammonia-oxidizing bacteria (r = 0.984, p < 0.001), which was the main driver of nitrification. During the wet season, soil nitrate (NO₃^?) and soil organic matter (SOC) were found positively correlated with N₂O emissions (r = 0.774, p = 0.041 and r = 0.827, p = 0.015, respectively). The nirS gene showed a similar trend with N₂O fluxes. These results show the relationship between the abundance of soil microbes and N₂O emissions and suggest that N₂O emissions during the dry season were due to nitrification, whereas in wet season, denitrification might dominate N₂O emission.     

Wheat straw and its biochar had contrasting effects on soil C and N cycling two growing seasons after addition to a Black Chernozemic soil planted to barley

Application of crop residues and its biochar produced through slow pyrolysis can potentially increase carbon (C) sequestration in agricultural production systems. The impact of crop residue and its biochar addition on greenhouse gas emission rates and the associated changes of soil gross N transformation rates in agricultural soils are poorly understood. We evaluated the effect of wheat straw and its biochar applied to a Black Chernozemic soil planted to barley, two growing seasons or 15 months (at the full-bloom stage of barley in the second growing season) after their field application, on CO₂ and N₂O emission rates, soil inorganic N and soil gross N transformation rates in a laboratory incubation experiment. Gross N transformation rates were studied using the ¹⁵N isotope pool dilution method. The field experiment included four treatments: control, addition of wheat straw (30 t ha^?1), addition of biochar pyrolyzed from wheat straw (20 t ha^?1), and addition of wheat straw plus its biochar (30 t ha^?1 wheat straw + 20 t ha^?1 biochar). Fifteen months after their application, wheat straw and its biochar addition increased soil total organic C concentrations (p?=?0.039 and <0.001, respectively) but did not affect soil dissolved organic C, total N and NH₄ ⁺-N concentrations, and soil pH. Biochar addition increased soil NO₃ ^?-N concentrations (p?=?0.004). Soil CO₂ and N₂O emission rates were increased by 40 (p?p?=?0.03), respectively, after wheat straw addition, but were not affected by biochar application. Straw and its biochar addition did not affect gross and net N mineralization rates or net nitrification rates. However, biochar addition doubled gross nitrification rates relative to the control (p?2 and N₂O emissions and enhance soil C sequestration. However, the implications of the increased soil gross nitrification rate and NO₃ ^?-N in the biochar addition treatment for long-term NO₃ ^?-N dynamics and N₂O emissions need to be further studied.     

施肥对夏玉米季紫色土N2O排放及反硝化作用的影响

采用原状土柱-乙炔抑制培养法研究了施肥对紫色土玉米生长季土壤N2O排放通量和反硝化作用的影响.结果表明:玉米季施肥显著增加土壤N2O排放和反硝化损失,同时,各施肥处理间N2O排放与反硝化损失量差异显著.猪厩肥、猪厩肥配施氮磷钾肥、氮肥、氮磷钾肥和秸秆配施氮磷钾肥等处理的土壤N,O排放量分别为3.01、2.86、2.51、2.19和1.88 kg hm-2,分别占当季氮肥施用量的1.63％、1.53％、1.30％、1.09％和0.88％,反硝化损失量分别为6.74、6.11、5.23、4.69和4.12 kg hm-2,分别占当季氮肥施用量的3.97％、3.55％、2.97％、2.61％和2.23％,不施肥土壤的N2O排放量和反硝化损失量仅为0.56和0.78 kg hm-2.施肥是紫色土玉米生长前期(2周内)土壤N2O排放和反硝化速率出现高峰的主要驱动因子,土壤铵态氮和硝态氮含量是影响土壤N2O排放、土壤硝化和反硝化作用的限制因子,土壤含水量是重要影响因子,降雨是主要促发因素.土壤N2O排放量与反硝化损失量的比值介于0.45 ～0.72之间,土壤反硝化损失量极显著高于土壤N2O排放量,说明土壤反硝化作用是紫色土玉米生长季氮肥损失的重要途径.     

Effects of land-use type and nitrogen addition on nitrous oxide and carbon dioxide production potentials in Japanese Andosols

Land-use type and nitrogen (N) addition strongly affect nitrous oxide (N₂O) and carbon dioxide (CO₂) production, but the impacts of their interaction and the controlling factors remain unclear. The aim of this study was to evaluate the effect of both factors simultaneously on N₂O and CO₂ production and associated soil chemical and biological properties. Surface soils (0–10 cm) from three adjacent lands (apple orchard, grassland and deciduous forest) in central Japan were selected and incubated aerobically for 12 weeks with addition of 0, 30 or 150 kg N ha^–1 yr^–1. Land-use type had a significant (p < 0.001) impact on the cumulative N₂O and CO₂ production. Soils from the apple orchard had higher N₂O and CO₂ production potentials than those from the grassland and forest soils. Soil net N mineralization rate had a positive correlation with both soil N₂O and CO₂ production rates. Furthermore, the N₂O production rate was positively correlated with the CO₂ production rate. In the soils with no N addition, the dominant soil properties influencing N₂O production were found to be the ammonium-N content and the ratio of soil microbial biomass carbon to nitrogen (MBC/MBN), while those for CO₂ production were the content of nitrate-N and soluble organic carbon. N₂O production increased with the increase in added N doses for the three land-use types and depended on the status of the initial soil available N. The effect of N addition on CO₂ production varied with land use type; with the increase of N addition doses, it decreased for the apple orchard and forest soils but increased for the grassland soils. This difference might be due to the differences in microbial flora as indicated by the MBC/MBN ratio. Soil N mineralization was the major process controlling N₂O and CO₂ production in the examined soils under aerobic incubation conditions.     

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).     

不同碳源添加对钙质土高累积硝态氮向土壤有机氮库转化的研究

Excessive amounts of nitrate have accumulated in many soils on the North China Plain due to the large amounts of chemical N fertilizers or manures used in combination with low carbon inputs. We investigated the potential of different carbon substrates added to transform soil nitrate into soil organic N (SON). A 56-d laboratory incubation experiment using the 15 N tracer (K15 NO3 ) technique was carried out to elucidate the proportion of SON derived from accumulated soil nitrate following amendment with glucose or maize straw at controlled soil temperature and moisture. The dynamics and isotopic abundance of mineral N (NO3 and NH+4 ) and SON and greenhouse gas (N2O and CO2 ) emissions during the incubation were investigated. Although carbon amendments markedly stimulated transformation of nitrate to newly formed SON, this was only a substitution effect of the newly formed SON with native SON because SON at the end of the incubation period was not significantly different (P > 0.05) from that in control soil without added C. At the end of the incubation period, amendment with glucose, a readily available C source, increased nitrate immobilization by 2.65 times and total N2O-N emission by 33.7 times, as compared with maize straw amendment. Moreover, the differences in SON and total N2O-N emission between the treatments with glucose and maize straw were significant (P < 0.05). However, the total N2O-N emission in the straw treatment was not significantly (P > 0.05) greater than that in the control. Straw amendment may be a potential option in agricultural practice for transformation of nitrate N to SON and minimization of N2O emitted as well as restriction of NO3-N leaching.     

Denitrification in grass swards is increased under elevated atmospheric CO2

Emissions of N₂O and N₂ were measured from Lolium perenne L. swards under ambient (36 Pa) and elevated (60 Pa) atmospheric CO₂ at the Swiss free air carbon dioxide enrichment experiment following application of 11.2 g N m⁻² as ¹⁵NH₄¹⁵NO₃ or ¹⁴NH₄¹⁵NO₃ (1 at.% excess ¹⁵N). Total denitrification (N₂O+N₂) was increased under elevated pCO₂ with emissions of 6.2 and 19.5 mg ¹⁵N m⁻² measured over 22 d from ambient and elevated pCO₂ swards, respectively, supporting the hypothesis that increased belowground C allocation under elevated pCO₂ provides the energy for denitrification. Nitrification was the predominant N₂O producing process under ambient pCO₂ whereas denitrification was predominant under elevated pCO₂. The N₂-to-N₂O ratio was often higher under elevated pCO₂ suggesting that previous estimates of gaseous N losses based only on N₂O emissions have greatly underestimated the loss of N by denitrification.     

Denitrification and C,N mineralization as function of temperature and moisture potential in organic and mineral horizons of an acid spruce forest soil

The influence of temperature (T) and water potential (ψ) on the denitrification potential, C and N mineralization and nitrification were studied in organic and mineral horizons of an acid spruce forest soil. The amount of N₂O emitted from organic soil was 10 times larger than from the mineral one. The maximum of N₂O emission was in both soils at the highest water potential 0 MPa and at 20°C. CO₂ production in the organic soil was 2 times higher than in mineral soil. Net ammonification in organic soil was negative for most of the T‒ψ variations, while in mineral soil it was positive. Net nitrification in organic soil was negative only at the maximum water potential and temperature (0 MPa, 28°C). The highest rate was between 0 and −0.3 MPa and between 20 and 28°C. In mineral soil NO₃⁻ accumulated at all T‒ψ variations with a maximum at 20^oC and −0.3 MPa. We concluded that in organic soil the immobilization of NH₄⁺ is the dominant process in the N‒cycling. Nevertheless, decreasing of total N mineralized at 0 MPa and 20—28^oC can be explained by denitrification.     

Nitrate Transformation and N2O Emission in a Typical Intensively Managed Calcareous Fluvaquent Soil: A 15-Nitrogen Tracer Incubation Study

A 56-day aerobic incubation experiment was performed with 15-nitrogen (N) tracer techniques after application of wheat straw to investigate nitrate-N (NO₃-N) immobilization in a typical intensively managed calcareous Fluvaquent soil. The dynamics of concentration and isotopic abundance of soil N pools and nitrous oxide (N₂O) emission were determined. As the amount of straw increased, the concentration and isotopic abundance of total soil organic N and newly formed labeled particulate organic matter (POM-N) increased while NO₃-N decreased. When ¹⁵NO₃-N was applied combined with a large amount of straw at 5000 mg carbon (C) kg^?1 only 1.1 ± 0.4 mg kg^?1 NO₃-N remained on day 56. The soil microbial biomass N (SMBN) concentration and newly formed labeled SMBN increased significantly (P < 0.05) with increasing amount of straw. Total N₂O-N emissions were at levels of only micrograms kg^?1 soil. The results indicate that application of straw can promote the immobilization of excessive nitrate with little emission of N₂O.     

Soil carbon dioxide fluxes in established switchgrass land managed for biomass production

Switchgrass (Panicum virgatum L.) grown for biomass feedstock production has the potential to increase soil C sequestration, and soil CO₂ flux in grassland is an important component in the global C budget. The objectives of this study were to: (1) determine the effects of N fertilization and harvest frequency on soil CO₂ flux, soil microbial biomass carbon (SMBC), and potentially mineralizable carbon (PMC); and (2) evaluate the relationship of soil CO₂ flux with soil temperature, soil moisture, SMBC, and PMC. Two N rates (0 and 224 kg ha⁻¹) were applied as NH₄NO₃ and cattle (Bos Taurus L.) manure. Switchgrass was harvested every year at anthesis or alternate years at anthesis. The data were collected during growing season (May-October) 2001-2004 on switchgrass-dominated Conservation Reserve Program (CRP) land in east-central South Dakota, USA. Manure application increased soil CO₂ flux, SMBC, and PMC during the early portion of the growing season compared with the control, but NH₄NO₃ application did not affect soil CO₂ flux, SMBC, and PMC. However, seasonal variability of soil CO₂ flux was not related to SMBC and PMC. Estimated average soil CO₂ fluxes during the growing periods were 472, 488, and 706 g CO₂-C m⁻² for control, NH₄NO₃-N, and manure-N plots, respectively. Switchgrass land with manure application emitted more CO₂, and approximately 45% of the C added with manure was respired to the atmosphere. Switchgrass harvested at anthesis decreased soil CO₂ flux during the latter part of the growing season, and flux was lower under every year harvest treatment than under alternate years harvest. Soil temperature was the most significant single variable to explain the variability in soil CO₂ flux. Soil water content was not a limiting factor in controlling seasonal CO₂ flux.     

尿素和KNO3对水稻土无机氮转化过程和产物的影响Ⅱ.N2O生成过程

采用15N技术标记尿素和KNO3,研究了淹水条件下黄泥土和红壤性水稻土生成N2 O的主要过程。结果表明 ,黄泥土反硝化过程产物以N2 为主 ,N2 O的生成量可以略而不计。加入KNO3促进NO- 3异化还原成铵过程 ,从而增加N2 O生成速率。红壤性水稻土主要通过反硝化或好气反硝化过程生成N2 O ,随着土壤pH的提高或NO- 3 浓度升高 ,N2 O生成速率增大。无论是黄泥土还是红壤性水稻土 ,有相当一部分样本的N2 O的15N丰度在NO- 2 、NO- 3 、NH 4的15N丰度范围外 ,由此推论 ,氮转化生成N2 O的过程应在微生物细胞内进行。     

Sequential reduction of nitrate and nitrous oxide under field conditions as brought about by organic amendments and irrigation management

The effect of organic amendments and irrigation management in the field were studied with respect to E_h, NO₃^?, and soluble organic C concentrations in the soil solution, and gaseous concentrations of N₂O, CO₂, and the ratio N₂ to O₂. Duplicate plots were treated with fresh bovine manure as follows: control 45t·ha^?1, 180 t·ha^?1 with a standard irrigation cycle (SI), and 180 t·ha^?1 with a double irrigation (DI). Samples to 230cm were obtained at several depths in each profile during the 84-day study. The general order for treatment effects upon CO₂ concentrations and soluble C was the same: SI > DI > 45 t·ha^?1 > control. The order for N₂/O₂ was 180 t·ha^?1 (SI and DI) > 45 t·ha^?1 and control. The order for both N₂O and NO^?1 was the same: 45 t.ha^?1 and DI > SI and control. The most important factor affecting N₂O concentrations was the NO₃^? concentration; soil solution concentrations greater than 16 μN·ml^?1 had much higher frequencies of high N₂O concentrations. The sequential reduction of NO^?1₃→ N₂O → N₂ was noted in all treatments by the following observations: (i) the concentrations of both NO^?₃ and N₂O were highest at the beginning of the experiment; (ii) the concentrations of CO₂ and N₂/O₂ were higher near the end: (iii) sub-ambient concentrations of N₂O were more frequent near the end of the study. Use of N₂O as an indicator of denitrification is cautioned since one of the highest manured treatments (SI) had N₂O concentrations no different than the control, but had much higher CO₂ and N₂/O₂ concentrations and more reduced (E_h) conditions. We conclude that use of a single irrigation method is far superior to the double irrigation method with respect to reducing losses of NO₃^? and N₂O and for conserving organic N arid water.     

Effects of rainfall pattern on carbon and nitrogen dynamics in soil amended with biogas slurry and composted cattle manure

Soil moisture affects the degradation of organic fertilizers in soils considerably, but less is known about the importance of rainfall pattern on the turnover of C and N. The objective of this study was to determine the effects of different rainfall patterns on C and N dynamics in soil amended with either biogas slurry (BS) or composted cattle manure (CM). Undisturbed soil cores without (control) or with BS or CM, which were incorporated at a rate of 100 kg N ha^–1, were incubated for 140 d at 13.5°C. Irrigation treatments were (1) continuous irrigation (cont_irr; 3 mm d^–1); (2) partial drying and stronger irrigation (part_dry; no irrigation for 3 weeks, 1 week with 13.5 mm d^–1), and (3) periodic heavy rainfall (hvy_rain; 24 mm d^–1 every 3 weeks for 1 d and 2 mm d^–1 for the other days). The average irrigation was 3 mm d^–1 in each treatment. Cumulative emissions of CO₂ and N₂O from soils amended with BS were 92.8 g CO₂‐C m^–2 and 162.4 mg N₂O‐N m^–2, respectively, whereas emissions from soils amended with CM were 87.8 g CO₂‐C m^–2 and only 38.9 mg N₂O‐N m^–2. While both organic fertilizers significantly increased CO₂ production compared to the control, N₂O emissions were only significantly increased in the BS‐amended soil. Under the conditions of the experiment, the rainfall pattern affected the temporal production of CO₂ and N₂O, but not the cumulative emissions. Cumulative NO leaching was highest in the BS‐amended soils (9.2 g NO ‐N m^–2) followed by the CM‐amended soil (6.1 g NO ‐N m^–2) and lowest in the control (4.7 g NO ‐N m^–2). Nitrate leaching was also independent of the rainfall pattern. Our study shows that rainfall pattern may not affect CO₂ and N₂O emissions and NO leaching markedly provided that the soil does not completely dry out.     

Dynamics of maize (Zea mays L.) leaf straw mineralization as affected by the presence of soil and the availability of nitrogen

An incubation experiment was carried out with maize (Zea mays L.) leaf straw to analyze the effects of mixing the residues with soil and N amendment on the decomposition process. In order to distinguish between soil effects and nitrogen effects for both the phyllospheric microorganisms already present on the surface of maize straw and soil microorganisms the N amendment was applied in two different placements: directly to the straw or to the soil. The experiment was performed in dynamic, automated microcosms for 22 days at 15 °C with 7 treatments: (1) untreated soil, (2) non-amended maize leaf straw without soil, (3) N amended maize leaf straw without soil, (4) soil mixed with maize leaf straw, (5) N amended soil, (6) N amended soil mixed with maize leaf straw, and (7) soil mixed with N amended maize leaf straw. ¹⁵NH₄¹⁵NO₃ (5 at%) was added. Gas emissions (CO₂, ¹³CO₂ and N₂O) were continuously recorded throughout the experiment. Microbial biomass C, biomass N, ergosterol, δ¹³C of soil organic C and of microbial biomass C as well as ¹⁵N in soil total N, mineral N and microbial biomass N were determined in soil samples at the end of the incubation. The CO₂ evolution rate showed a lag-phase of two days in the non-amended maize leaf straw treatment without soil, which was completely eliminated when mineral N was added. The addition of N generally increased the CO₂ evolution rate during the initial stages of maize leaf straw decomposition, but not the cumulative CO₂ production. The presence of soil caused roughly a 50% increase in cumulative CO₂ production within 22 days in the maize straw treatments due to a slower decrease of CO₂ evolution after the initial activity peak. Since there are no limitations of water or N, we suggest that soil provides a microbial community ensuring an effective succession of straw decomposing microorganisms. In the treatments where maize and soil was mixed, 75% of microbial biomass C was derived from maize. We concluded that this high contribution of maize using microbiota indicates a strong influence of organisms of phyllospheric origin to the microbial community in the soil after plant residues enter the soil.