Effects of carbon and phosphorus addition on microbial respiration,N<Subscript>2</Subscript>O emission,and gross nitrogen mineralization in a phosphorus-limited grassland soil

Soil microbes are frequently limited by carbon (C), but also have a high phosphorus (P) requirement. Little is known about the effect of P availability relative to the availability of C on soil microbial activity. In two separate experiments, we assessed the effect of P addition (20 mg P kg^?1 soil) with and without glucose addition (500 mg C kg^?1 soil) on gross nitrogen (N) mineralization (¹⁵N pool dilution method), microbial respiration, and nitrous oxide (N₂O) emission in a grassland soil. In the first experiment, soils were incubated for 13 days at 90% water holding capacity (WHC) with addition of NO₃^? (99 mg N kg^?1 soil) to support denitrification. Addition of C and P had no effect on gross N mineralization. Initially, N₂O emission significantly increased with glucose, but it decreased at later stages of the incubation, suggesting a shift from C to NO₃^? limitation of denitrifiers. P addition increased the N₂O/CO₂ ratio without glucose but decreased it with glucose addition. Furthermore, the ¹⁵N recovery was lowest with glucose and without P addition, suggesting a glucose by P interaction on the denitrifying community. In the second experiment, soils were incubated for 2 days at 75% WHC without N addition. Glucose addition increased soil ¹⁵N recovery, but had no effect on gross N mineralization. Possibly, glucose addition increased short-term microbial N immobilization, thereby reducing N-substrates for nitrification and denitrification under more aerobic conditions. Our results indicate that both C and P affect N transformations in this grassland soil.     

Contrasting response of two grassland soils to N addition and moisture levels: N<Subscript>2</Subscript>O emission and functional gene abundance

Purpose

Nitrification and denitrification processes dominate nitrous oxide (N₂O) emission in grassland ecosystems, but their relative contribution as well as the abiotic factors are still not well understood.

Materials and methods

Two grassland soils from Duolun in Inner Mongolia, China, and Canterbury in New Zealand were used to quantitatively compare N₂O production and the abundance of bacterial and archaeal amoA, denitrifying nirK and nirS genes in response to N additions (0 and 100 μg NH₄ ⁺–N g^?1 dry soil) and two soil moisture levels (40 and 80 % water holding capacity) using microcosms.

Results and discussion

Soil moisture rather than N availability significantly increased the nitrification rate in the Duolun soil but not in the Canterbury soil. Moreover, N addition promoted denitrification enzyme activities in the Canterbury soil but not in the Duolun soil. The abundance of bacterial and archaeal amoA genes significantly increased as soil moisture increased in the Duolun soil, whereas in the Canterbury soil, only the abundance of bacterial amoA gene increased. The increase in N₂O flux induced by N addition was significantly greater in the Duolun soil than in the Canterbury soil, suggesting that nitrification may have a dominant role in N₂O emission for the Duolun soil, while denitrification for the Canterbury soil.

Conclusions

Microbial processes controlling N₂O emission differed in grassland soils, thus providing important baseline data in terms of global change.

     

Effects of biochar,earthworms, and litter addition on soil microbial activity and abundance in a temperate agricultural soil

Biochar application to arable soils could be effective for soil C sequestration and mitigation of greenhouse gas (GHG) emissions. Soil microorganisms and fauna are the major contributors to GHG emissions from soil, but their interactions with biochar are poorly understood. We investigated the effects of biochar and its interaction with earthworms on soil microbial activity, abundance, and community composition in an incubation experiment with an arable soil with and without N-rich litter addition. After 37 days of incubation, biochar significantly reduced CO₂ (up to 43 %) and N₂O (up to 42 %), as well as NH₄ ⁺-N and NO₃ ^?-N concentrations, compared to the control soils. Concurrently, in the treatments with litter, biochar increased microbial biomass and the soil microbial community composition shifted to higher fungal-to-bacterial ratios. Without litter, all microbial groups were positively affected by biochar × earthworm interactions suggesting better living conditions for soil microorganisms in biochar-containing cast aggregates after the earthworm gut passage. However, assimilation of biochar-C by earthworms was negligible, indicating no direct benefit for the earthworms from biochar uptake. Biochar strongly reduced the metabolic quotient qCO₂ and suppressed the degradation of native SOC, resulting in large negative priming effects (up to 68 %). We conclude that the biochar amendment altered microbial activity, abundance, and community composition, inducing a more efficient microbial community with reduced emissions of CO₂ and N₂O. Earthworms affected soil microorganisms only in the presence of biochar, highlighting the need for further research on the interactions of biochar with soil fauna.     

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.     

The effects of rice (Oryza sativa L. ssp. japonica) husk biochar on nitrogen dynamics during the decomposition of hairy vetch in two soils under high-soil moisture condition

ABSTRACT

Legumes, including hairy vetch (Vicia villosa Roth), are widely used as green manures. They fix nitrogen (N) and provide the N to other crops when they decompose, and thus are considered alternatives for chemical N fertilizers. However, N-rich plant residues, including hairy vetch, are also sources of soil nitrous oxide (N₂O) emissions, a greenhouse gas. On one hand, rice (Oryza sativa L. ssp. japonica) husk biochar is widely used as a soil conditioner in Japan and has been reported as a tool to mitigate soil N₂O emissions. We conducted a soil core incubation experiment (1.5 months) to compare the N₂O emissions during the decomposition of surface-applied hairy vetch (0.8 kg dried hairy vetch m^?2 soil) under semi-saturated soil moisture conditions (~100% water-filled pore space (WFPS)), using two soil types, namely Andosol and Fluvisol. Throughout the incubation period, the use of biochar suppressed soil NH₄⁺-N concentrations in Andosol, whereas the effect of biochar on NH₄⁺-N was not clear in Fluvisol. Biochar increased the nitrate (NO₃^?-N) levels both in Andosol and Fluvisol, suggesting a negative influence on denitrification and/or a positive influence on nitrification. Biochar application did not influence the cumulative N₂O emissions. Our study suggests that rice husk biochar is not a good option to mitigate N₂O emissions during the decomposition of surface-applied hairy vetch, although this study was performed under laboratory conditions without plants. However, the trends of the inorganic-N concentration changes followed by the addition of hairy vetch and biochar were markedly different between the two soil types. Thus, factors behind the differences need to be further studied.     

生物质炭对土壤N2O消耗的影响及其微生物影响机理

生物质炭在温室气体减排方面具有很大的发展前景,它不仅能实现固碳,对于在大气中停留时间长且增温潜势大的N₂O也能发挥积极作用。本研究采用室内厌氧培养试验,按照生物质炭与土壤质量比（0、1%和5%）加入一定量生物质炭,土壤重量含水率控制在20%。利用Robotized Incubation平台实时检测N₂O和N₂浓度变化,通过测定土壤中反硝化功能基因丰度（nirK、nirS、nosZ）分析生物质炭对N₂O消耗的影响及其微生物方面的影响机理。结果表明：经过20 h厌氧培养后,0生物质炭处理的反硝化功能基因丰度（基因拷贝数·g^-1）分别为6.80×10⁷（nirK）、5.59×10⁸（nirS）和1.22×10⁸（nosZ）。与0生物质炭处理相比,1%生物质炭处理的nirS基因丰度由最初的2.65×10⁸基因拷贝数·g^-1升至7.43×10⁸基因拷贝数·g^-1,nosZ基因丰度则提高了一个数量级,由4.82×10⁷基因拷贝数·g^-1升至1.50×10⁸基因拷贝数·g^-1,然而nirK基因丰度并无明显变化;5%生物质炭处理的反硝化功能基因丰度并未发生显著变化。试验结束时,添加生物质炭处理的N₂/（N₂O+N₂）比值也明显高于0生物质炭处理。相关性分析结果表明,nirS基因丰度和nosZ基因丰度均与N₂O浓度在0.01水平上显著相关。试验末期nirS基因丰度和nosZ基因丰度均随着N₂O浓度的降低而升高。因此在本试验中,添加1%生物质炭可显著提高nirS和nosZ基因型反硝化细菌的丰度,增大N₂/（N₂O+N₂）比值,促进N₂O彻底还原成N₂。生物质炭对于N₂O主要影响机理是增大了可以还原氧化亚氮的细菌活性,促进完全反硝化。     

The effect of temperature and moisture on the source of N<Subscript>2</Subscript>O and contributions from ammonia oxidizers in an agricultural soil

In recent years, identification of the microbial sources responsible for soil N₂O production has substantially advanced with the development of isotope enrichment techniques, selective inhibitors, mathematical models and the discoveries of specific N-cycling functional genes. However, little information is available to effectively quantify the N₂O produced from different microbial pathways (e.g. nitrification and denitrification). Here, a ¹⁵N-tracing incubation experiment was conducted under controlled laboratory conditions (50, 70 and 85% water-filled pore space (WFPS) at 25 and 35 °C). Nitrification was the main contributor to N₂O production. At 50, 70 and 85% WFPS, nitrification contributed 87, 80 and 53% of total N₂O production, respectively, at 25 °C, and 86, 74 and 33% at 35 °C. The proportion of nitrified N as N₂O (P _N2O) increased with temperature and moisture, except for 85% WFPS, when P _N2O was lower at 35 °C than at 25 °C. Ammonia-oxidizing archaea (AOA) were the dominant ammonia oxidizers, but both AOA and ammonia-oxidizing bacteria (AOB) were related to N₂O emitted from nitrification. AOA and AOB abundance was significantly influenced by soil moisture, more so than temperature, and decreased with increasing moisture content. These findings can be used to develop better models for simulating N₂O from nitrification to inform soil management practises for improving N use efficiency.     

Nitrogen Removal and N<Subscript>2</Subscript>O Emission During Low Carbon Wastewater Treatment Using the Multiple A/O Process

With the organic carbon of acetate (SBR-A) and propionate (SBR-P), the effect of organic carbon sources on nitrogen removal and nitrous oxide (N₂O) emission in the multiple anoxic and aerobic process was investigated. The nitrogen removal percentages in SBR-A and SBR-P reactor were both 72%, and the phosphate removal percentages were 97 and 85.4%, respectively. During nitrification, both the NH₄ ⁺-N oxidation rate in the SBR-A and SBR-P had a small change without the influence of the addition of nitrite nitrogen (NO₂ ^?-N). With the addition of 10 mg/L NO₂ ^?-N, the nitrate nitrogen (NO₃ ^?-N) production rate, N₂O accumulation rate and emission factor had increased. At the same time, the N₂O emission factor of SBR-A and SBR-P reactors increased from 2.13 and 0.87% to 4.66 and 2.08%, respectively. During exogenous denitrification, when nitrite was used as electron acceptor, the N₂O emission factors were 34.1 and 8.6 times more than those of NO₃ ^?-N as electron acceptor in SBR-A and SBR-P. During endogenous denitrification with NO₂ ^?-N as electron acceptor, the accumulation rate and emission factor of N₂O were higher than those of NO₃ ^?-N as electron acceptor. High-throughput sequencing test showed that the dominant bacteria were Proteobacteria and Bacteroidetes in both reactors at the phylum level, while the main denitrification functional bacteria were Thauera sp., Zoogloea sp. and Dechloromonas sp. at the genus level.     

Reduction de l'oxyde nitreux dans les sols de rizieres du senegal: Mesure de l'activite denitrifiante

A new method to estimate the rate of denitrification in soil was developed, and two different activities were measured: (1) the initial (or true) denitrifying activity of the soil under prevailing conditions; (2) the potential denitrifying activity induced by the addition of N₂O. Less than 50 g of soil, saturated with water, were incubated anaerobically at 37°C, with a known amount of N₂O, and the disappearance of N₂O was followed by gas chromatography. In 25 paddy soils of Senegal, a highly positive rank correlation was found to exist between the denitrifying activity measured by chromatographic and respirometric methods, under the same conditions of incubation with either N₂O or NO₃^? as the hydrogen acceptor. By the N₂O reduction method, it was found that there was no initial denitrifying activity in the rhizosphere of 3-week-old rice.     

Evaluating the effect of liming on N<Subscript>2</Subscript>O fluxes from denitrification in an Andosol using the acetylene inhibition and <Superscript>15</Superscript>N isotope tracer methods

We assessed the effect of liming on (1) N₂O production by denitrification under aerobic conditions using the ¹⁵N tracer method (experiment 1); and (2) the reduction of N₂O to N₂ under anaerobic conditions using the acetylene inhibition method (experiment 2). A Mollic Andosol with three lime treatments (unlimed soil, 4 and 20 mg CaCO₃ kg^?1) was incubated at 15 and 25 °C for 22 days at 50% and then 80% WFPS with or without 200 mg N kg^?1 added as ¹⁵N enriched KNO₃ in experiment 1. In experiment 2, the limed and unlimed soils were incubated under completely anaerobic conditions for 44 h (with or without 100 mg N kg^?1 as KNO₃). In experiment 1, limed treatments increased N₂O fluxes at 50% WFPS but decreased these fluxes at 80% WFPS. At 25 °C, cumulative N₂O and ¹⁵N₂O emissions in the high lime treatment were the lowest (with at least 30% less ¹⁵N₂O and total N₂O than the unlimed soil). Under anaerobic conditions, the high lime treatment showed at least 50% less N₂O than the unlimed treatment at both temperatures with or without KNO₃ addition but showed enhanced N₂ production. Our results suggest that the positive effect of liming on the mitigation of N₂O evolution from soil was influenced by soil temperature and moisture conditions.     

Straw amendment to paddy soil stimulates denitrification but biochar amendment promotes anaerobic ammonia oxidation

Purpose

Organic matter amendment is usually used to improve soil physicochemical properties and to sequester carbon for counteracting climate change. There is no doubt that such amendment will change microbial activity and soil nitrogen transformation processes. However, the effects of straw and biochar amendment on anammox and denitrification activity and on community structure in paddy soil are unclear.

Materials and methods

We conducted a 30-day pot experiment using rice straw and rice straw biochar to deepen our understanding about the activity, microbial abundance, and community structure associated with soil nitrogen cycling during rice growth.

Results and discussion

Regarding activity, anammox contributed 3.1–8.1% of N₂ production and denitrification contributed 91.9–96.9% of N₂ production; straw amendment resulted in the highest denitrification rate (38.9 nmol N g^?1 h^?1), while biochar amendment resulted in the highest anammox rate (1.60 nmol N g^?1 h^?1). Both straw and biochar amendments significantly increased the hzsB and nosZ gene abundance (p < 0.05). Straw amendment showed the highest nosZ gene abundance, while biochar amendment showed the highest hzsB gene abundance. Phylogenetic analysis of the anammox bacteria 16S rRNA genes indicated that Candidatus Brocadia and Kuenenia were the dominant genera detected in all treatments.

Conclusions

Straw and biochar amendments have different influences on anaerobic ammonia oxidation and denitrification within paddy soil. Our results suggested that the changes in denitrification and anammox rates in the biochar and straw treatments were mainly linked to functional gene abundance rather than microbial community structure and that denitrification played the more major role in N₂ production in paddy soil.

     

Effect of biochar and nitrapyrin on nitrous oxide and nitric oxide emissions from a sandy loam soil cropped to maize

A field experiment was conducted to evaluate the combined or individual effects of biochar and nitrapyrin (a nitrification inhibitor) on N₂O and NO emissions from a sandy loam soil cropped to maize. The study included nine treatments: addition of urea alone or combined with nitrapyrin to soils that had been amended with biochar at 0, 3, 6, and 12 t ha^?1 in the preceding year, and a control without the addition of N fertilizer. Peaks in N₂O and NO flux occurred simultaneously following fertilizer application and intense rainfall events, and the peak of NO flux was much higher than that of N₂O following application of basal fertilizer. Mean emission ratios of NO/N₂O ranged from 1.11 to 1.72, suggesting that N₂O was primarily derived from nitrification. Cumulative N₂O and NO emissions were 1.00 kg N₂O-N ha^?1 and 1.39 kg NO-N ha^?1 in the N treatment, respectively, decreasing to 0.81–0.85 kg N₂O-N ha^?1 and 1.31–1.35 kg NO-N ha^?1 in the biochar amended soils, respectively, while there was no significant difference among the treatments. NO emissions were significantly lower in the nitrapyrin treatments than in the N fertilization-alone treatments (P?<?0.05), but there was no effect on N₂O emissions. Neither biochar nor nitrapyrin amendment affected maize yield or N uptake. Overall, our results showed that biochar amendment in the preceding year had little effect on N₂O and NO emissions in the following year, while the nitrapyrin decreased NO, but not N₂O emissions, probably due to suppression of denitrification caused by the low soil moisture content.     

Effects of biochar addition on N<Subscript>2</Subscript>O and CO<Subscript>2</Subscript> emissions from two paddy soils

Impacts of biochar addition on nitrous oxide (N₂O) and carbon dioxide (CO₂) emissions from paddy soils are not well documented. Here, we have hypothesized that N₂O emissions from paddy soils could be depressed by biochar incorporation during the upland crop season without any effect on CO₂ emissions. Therefore, we have carried out the 60-day aerobic incubation experiment to investigate the influences of rice husk biochar incorporation (50 t ha⁻¹) into two typical paddy soils with or without nitrogen (N) fertilizer on N₂O and CO₂ evolution from soil. Biochar addition significantly decreased N₂O emissions during the 60-day period by 73.1% as an average value while the inhibition ranged from 51.4% to 93.5% (P < 0.05–0.01) in terms of cumulative emissions. Significant interactions were observed between biochar, N fertilizer, and soil type indicating that the effect of biochar addition on N₂O emissions was influenced by soil type. Moreover, biochar addition did not increase CO₂ emissions from both paddy soils (P > 0.05) in terms of cumulative emissions. Therefore, biochar can be added to paddy fields during the upland crop growing season to mitigate N₂O evolution and thus global warming.     

田间老化生物质炭减缓稻麦轮作系统土壤N2O排放能力降低的机理

作为一种重要的土壤调节剂,生物质炭在固碳减排,尤其在氧化亚氮(N₂O)减排方面的作用日益突出。本研究通过田间定位试验,分析稻麦轮作体系新鲜和田间不同时间老化生物质炭对N₂O排放的影响,旨在明确生物质炭对田间N₂O排放的持续效应及其作用机理。试验共设置5个处理,分别为CK（不施氮肥和生物质炭）、N（施氮肥）、NB_0y（氮肥+新鲜生物质炭）、NB_2y（氮肥+2年老化生物质炭）和NB_5y （氮肥+5年老化生物质炭）,动态监测稻麦轮作周期N₂O排放,测定水稻和小麦收获后土壤理化性质和氮循环功能基因丰度。结果表明,生物质炭显著降低土壤N2O累积排放量32.4% ~ 54.0%,且表现为NB_0y> NB_2y> NB_5y。与N处理相比,NB_0y, NB_2y 和NB_5y处理显著提高土壤pH值0.6 ~ 1.2个单位、土壤有机碳（SOC）含量21.4 % ~ 58.6%、硝态氮（NO_3^--N）含量1.7% ~ 31.3%,对土壤pH改善能力随着生物质炭老化而下降。生物质炭处理显著提高nosZ基因丰度54.9% ~ 249.4%,土壤 (nirS+nirK)/nosZ比值随着生物质炭老化而增加。相关性分析表明,土壤N₂O累积排放量与pH值呈显著负相关,与NO_3^--N含量和amoA-AOB（氨氧化细菌）丰度呈显著正相关。因此,新鲜和田间不同时间老化生物质炭均能显著改善土壤理化特性,降低土壤 N₂O排放且新鲜生物质炭的作用效果优于老化生物质炭。土壤NO_3^--N 含量及(nirS+nirK)/nosZ比值的增加,是导致老化生物质炭减排N₂O能力降低的主要原因。     

Biochars immobilize soil cadmium, but do not improve growth of emergent wetland species Juncus subsecundus in cadmium-contaminated soil

Purpose

An addition of biochar mixed into the substrate of constructed wetlands may alleviate toxicity of metals such as cadmium (Cd) to emergent wetland plants, leading to a better performance in terms of pollutant removal from wastewater. The objective of this study was to investigate the impact of biochars on soil Cd immobilization and phytoavailability, growth of plants, and Cd concentration, accumulation, and translocation in plant tissues in Cd-contaminated soils under waterlogged conditions.

Materials and methods

A glasshouse experiment was conducted to investigate the effect of biochars derived from different organic sources (pyrolysis of oil mallee plants or wheat chaff at 550 °C) with varied application amounts (0, 0.5, and 5 % w/w) on mitigating Cd (0, 10, and 50 mg kg^?1) toxicity to Juncus subsecundus under waterlogged soil condition. Soil pH and CaCl₂/EDTA-extractable soil Cd were determined before and after plant growth. Plant shoot number and height were monitored during the experiment. The total root length and dry weight of aboveground and belowground tissues were recorded. The concentration of Cd in plant tissues was determined.

Results and discussion

After 3 weeks of soil incubation, pH increased and CaCl₂-extractable Cd decreased significantly with biochar additions. After 9 weeks of plant growth, biochar additions significantly increased soil pH and electrical conductivity and reduced CaCl₂-extractable Cd. EDTA-extractable soil Cd significantly decreased with biochar additions (except for oil mallee biochar at the low application rate) in the high-Cd treatment, but not in the low-Cd treatment. Growth and biomass significantly decreased with Cd additions, and biochar additions did not significantly improve plant growth regardless of biochar type or application rate. The concentration, accumulation, and translocation of Cd in plants were significantly influenced by the interaction of Cd and biochar treatments. The addition of biochars reduced Cd accumulation, but less so Cd translocation in plants, at least in the low-Cd-contaminated soils.

Conclusions

Biochars immobilized soil Cd, but did not improve growth of the emergent wetland plant species at the early growth stage, probably due to the interaction between biochars and waterlogged environment. Further study is needed to elucidate the underlying mechanisms.     

N<Subscript>2</Subscript>O production pathways relate to land use type in acidic soils in subtropical China

Purpose

Agricultural practises impact soil properties and N transformation rate, and have a greater effect on N₂O production pathways in agricultural soils compared with natural woodland soils. However, whether agricultural land use affects N₂O production pathways in acidic soils in subtropical regions remains unknown.

Materials and methods

In this study, we collected natural woodland soil (WD) and three types of agricultural soils, namely upland agricultural (UA), tea plantation (TP) and bamboo plantation (BP) soils. We performed paired ¹⁵N-tracing experiment to investigate the effects of land use types on N₂O production pathways in acidic soils in subtropical regions in China.

Results and discussion

The results revealed that heterotrophic nitrification is the dominant pathway of N₂O production in WD, accounting for 44.6 % of N₂O emissions, whereas heterotrophic nitrification contributed less than 2.7 % in all three agricultural soils, due to a lower organic C content and soil C/N ratio. In contrast, denitrification dominated N₂O production in agricultural soils, accounting for 54.5, 72.8 and 77.1 % in UA, TP and BP, respectively. Nitrate (NO₃ ^?) predominantly affected the contribution from denitrification in soils under different land use types. Autotrophic nitrification increased after the conversion of woodland to agricultural lands, peaking at 42.8 % in UA compared with only 21.5 % in WD, and was positively correlated with soil pH. Our data suggest that pH plays a great role in controlling N₂O emissions through autotrophic nitrification following conversion of woodland to agricultural lands.

Conclusions

Our results demonstrate the variability in N₂O production pathways in soils of different land use types. Soil pH, the quantity and quality of organic C and NO₃ ^? content primarily determined N₂O emissions. These results will likely assist modelling and mitigation of N₂O emissions from different land use types in subtropical acidic soils in China and elsewhere.

     

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.     

Diversity of denitrifying microflora and ability to reduce N2O in two soils

 The ozone-depleting gas N₂O is an intermediate in denitrification, the biological reduction of NO₃ ^– to the gaseous products N₂O and N₂ gas. The molar ratio of N₂O produced (N₂O/N₂O+N₂) varies temporally and spatially, and in some soils N₂O may be the dominant end product of denitrification. The fraction of NO₃ ^–-N emitted as N₂O may be due at least in part to the abundance and activity of denitrifying bacteria which possess N₂O reductase. In this study, we enumerated NO₃ ^–-reducing and denitrifying bacteria, and compared and contrasted collections of denitrifying bacteria isolated from two agricultural soils, one (Auxonne, soil A) with N₂O as the dominant product of denitrification, the other (Chalons, soil C) with N₂ gas as the dominant product. Isolates were tested for the ability to reduce N₂O, and the presence of the N₂O reductase (nosZ)-like gene was evaluated by polymerase chain reaction (PCR) using specific primers coupled with DNA hybridization using a specific probe. The diversity and phylogenetic relationships of members of the collections were established by PCR/restriction fragment length polymorphism of 16s rDNA. The two soils had similar numbers of bacteria which used NO₃ ^– as a terminal electron acceptor anaerobically. However, the soil A had many more denitrifiers which reduced NO₃ ^– to gaseous products (N₂O or N₂) than did soil C. Collections of 258 and 281 bacteria able to grow anaerobically in the presence of NO₃ ^– were isolated from soil A and soil C, respectively. These two collections contained 66 and 12 denitrifying isolates, respectively, the others reducing NO₃ ^– only as far as NO₂ ^–. The presence of nosZ sequences was generally a poor predictor of N₂O reducing ability: there was agreement between the occurrence of nosZ sequences and the N₂O reducing ability for only 42% of the isolates; 35% of the isolates (found exclusively in soil A) without detectable nosZ sequences reduced N₂O whereas 21% of the isolates carrying nosZ sequences did not reduce this gas under our assay conditions. Twenty-eight different 16S rDNA restriction patterns (using two restriction endonucleases) were distinguished among the 78 denitrifying isolates. Two types of patterns appeared to be common to both soils. Twenty-three and three types of patterns were found exclusively among bacteria isolated from soils A and C, respectively. The specific composition of denitrifying communities appeared to be different between the two soils studied. This may partly explain the differences in the behaviour of the soils concerning N₂O reduction during denitrification. Received: 31 October 1997     

Nitrogen transformation rates and N<Subscript>2</Subscript>O producing pathways in two pasture soils

Purpose

Better understanding of N transformations and the regulation of N₂O-related N transformation processes in pasture soil contributes significantly to N fertilizer management and development of targeted mitigation strategies.

Materials and methods

¹⁵N tracer technique combined with acetylene (C₂H₂) method was used to measure gross N transformation rates and to distinguish pathways of N₂O production in two Australian pasture soils. The soils were collected from Glenormiston (GN) and Terang (TR), Victoria, Australia, and incubated at a soil moisture content of 60% water-filled pore space (WFPS) and at temperature of 20 °C.

Results and discussion

Two tested pasture soils were characterized by high mineralization and immobilization turnover. The average gross N nitrification rate (n_tot) was 7.28 mg N kg^?1 day^?1 in TR soil () and 5.79 mg N kg^?1 day^?1 in GN soil. Heterotrophic nitrification rates (n_h), which accounting for 50.8 and 41.9% of n_tot, and 23.4 and 30.1% of N₂O emissions in GN and TR soils, respectively, played a role similar with autotrophic nitrification in total nitrification and N₂O emission. Denitrification rates in two pasture soils were as low as 0.003–0.004 mg N kg^?1 day^?1 under selected conditions but contributed more than 30% of N₂O emissions.

Conclusions

Results demonstrated that two tested pasture soils were characterized by fast N transformation rates of mineralization, immobilization, and nitrification. Heterotrophic nitrification could be an important NO₃^?–N production transformation process in studied pasture soils. Except for autotrophic nitrification, roles of heterotrophic nitrification and denitrification in N₂O emission in two pasture soils should be considered when developing mitigation strategies.

     

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.