Isotopic Model (NISOTOP) used to Investigate 15N-Urea Transformations in the Presence of Phenanthrene,Chrysene and Benzo(a)pyrene in a Soil–Plant System

An isotopic model (NISOTOP) has been developed to investigate the effect of the addition to soil of xenobiotics on urea hydrolysis, N mineralization and immobilization, nitrification and plant uptake of nitrogen in a soil-plant system, after addition of ¹⁵N enriched compounds. Therationale of the model follows from the errors in %¹⁵N abundance (^15N _D) and N concentration (C_N) determinations which cause high variability coefficients in the calculation of the amount of nitrogen present in the different compounds derived from the added ¹⁵N enriched urea. The extent of these errors, besides depending on C_N and ^15N _D errors, will also depend on natural ¹⁵N and ¹⁵N of the added compound, and therefore on the experimental conditions. The model is described by 18 first-order differential equations and is numerically solved by Euler's method with a time increment of 0.01 day. As an illustration, the model is applied to the effect of phenanthrene, chrysene and benzo(a)pyrene to a soil-plant system, following the addition of ¹⁵N-urea. These compounds have been chosen as examples of molecules having 3, 4 and 5 fused aromatic rings and are hereafter collectively referred to as PAHs. PAHs at the rate of 2 mg kg^-1 soiland ¹⁵N-urea at the rate of 166.7 mg N kg^-1 soil were added to wheat pots. At harvesting (after 14 days from plantation) the dry matter yield, the total N content and the N concentration of the wheat seedlings were not statistically affected by addition of the PAHs (P = 0.05). The efficiency of N uptake, that is the percentage of fertilizer taken up by the plants at harvesting in the absence of PAHs was 47.3%, while it was 11.7, 15.2 and 14.8% in the presence of phenanthrene, chrysene and benzo(a)pyrene,respectively. The computation of the first-order rate constants of the N transformations showed that N mineralization, nitrification and N-uptake were affected by the addition of phenanthrene, chrysene and benzo(a)pyrene, whilst benzo(a)pyrene inhibited urea hydrolysis more than phenanthrene and chrysene.     

Different responses of soil CO2 and N2O emissions to simulated N deposition in forests with divergent N transformation characteristics

CO₂ and N₂O are important greenhouse gases that are related to soil mineralization–immobilization turnover and nitrification. To explore the responses of CO₂ and N₂O emissions to N deposition in forests with different N transformation characteristics, CO₂ and N₂O fluxes were measured in two NH₄NO₃ fertilized plots. One plot was in a temperate pine plantation in Heilongjiang Liangshui National Nature Reserve (LS) with slow and minimally coupled mineralization–immobilization turnover and a high nitrification rate. The other plot was in a subtropical bamboo forest in the Fujian Daiyun Mountain National Nature Reserve (DY) in China with rapid and coupled mineralization–immobilization turnover but a low nitrification rate. The results showed that CO₂ emissions in the DY with a high mineralization rate were greater than those in the LS. Cumulative CO₂ emissions were significantly enhanced by N addition in DY, but in LS, they were not affected. The mean N₂O fluxes in the control were 0.010 and 0.008 mg N m^?2 hr^?1 for LS and DY, respectively. High N addition stimulated N₂O emissions in both LS and DY, but the response ratio for N₂O flux in LS (8.6) was larger than that in DY (2.9). These results suggested that soils with rapid and coupled mineralization–immobilization turnover are beneficial to CO₂ emissions and their positive response to N deposition. A high nitrification rate contributed to high N₂O emissions and the sensitive response of N₂O emissions to N deposition.     

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.     

Effect of tebuthiuron on soil N mineralization and nitrification

Abstract

Herbicides have potential for economical and efficient site preparation following timber harvest. The effects of tebuthiu‐ron, one of the herbicides approved for this use, on soil nitrogen (N) mineralization and nitrification were determined in laboratory incubations. Tebuthiuron was added at rates from 0 to 1000 μg g^‐1 to three soils. There was no effect of tebuthiuron additions of less than 1 μg g^‐1 on soil N mineralization and nitrification. Tebuthiuron reduced nitrification in all soils at 1000 μg g^‐1 and in two of the soils at 100 μg g^‐1 . All soils had increased net mineralization with tebuthiuron added at 100 and 1000 μg g^‐1. The addition of 50 μg NH⁺ ₄‐N and 1000 μg tebuthiuron g^‐1 resulted in increased net mineralization in the three soils. Nitrification was affected differently in each of the three soils by the addition of both NH⁺ ₄‐N and tebuthiuron. The added NH⁺ ₄‐N either removed the inhibition of nitrification by the herbicide or had no effect on the inhibition in two of the soils. In the third soil, nitrification was reduced by the addition of NH⁺ ₄‐N.

The presence of NO^‐ ₃‐N in these acid soils and the effects of added NH⁺ ₄‐N on NO^‐ ₃‐N production suggest that heterotrophic nitrification occurs in at least two of the soils. The findings of this study indicate that any effects of tebuthiuron on N mineralization and nitrification at the currently recommended application rates are likely to be transient and localized.     

Nitrogen transformations in an aerobic soil as determined by a 15NH4+ dilution technique

The rates of mineralization, immobilization and oxidation of N in an aerobic soil, an Andosol Brown, from the farm of the Hokkaido National Agricultural Experiment Station were simultaneously determined in the presence and absence of acetylene using a ¹⁵NH⁺₄ dilution technique. C₂H₂ inhibited nitrification, but did not directly affect mineralization and immobilization. Denitrification and immobilization of NO₃^?-N were negligible. Mineralization proceeded much faster than did immobilization. Net mineralization accounted for 22–59% of gross mineralization. The rates of N transformation at a water content of 60% were higher than those at 40%. The Q₁₀ values for mineralization, immobilization and nitrification were estimated, between 11° and 29°C, to be 2.0, 1.9 and 1.7, respectively.     

Immobilization and mineralization of nitrogen in soils incubated with pig slurry or ammonium sulphate

Nitrogen mineralization and immobilization were investigated in two soils incubated with ammonium sulphate or pig slurry over a range of temperatures and moisture contents. A reduction in the mineralization of soil organic N was observed in soils incubated with 100 μg NH₄⁺-Ng^?1 soil as ammonium sulphate at 30°C but not at lower temperatures. Addition of 100 μg NH₄⁺-N g^?1 soil as pig slurry resulted in a period of nett immobilization lasting up to 30 days at 5°C. Although the length of the immobilization phase was shorter at higher temperatures the total N immobilized was similar. The subsequent rate of mineralization in slurry-treated soils was not significantly greater (P = 0.05) than in untreated soils. There was no evidence of any subsequent increased mineralization arising from the immobilized N or slurry organic N for up to 175 days. The rate of immobilization was found to increase with increasing moisture content, though the period of nett immobilization was shorter, so that the amount of N immobilized was similar over a range of moisture contents from 10 to 40%. Approximately 40% of the NH₄⁺-N in the slurry was immobilized under the incubation conditions used.     

Impact of nitrogen and phosphorus additions on soil gross nitrogen transformations in a temperate desert steppe

Nutrient addition has a significant impact on plant growth and nutrient cycling. Yet, the understanding of how the addition of nitrogen (N) or phosphorus (P) significantly affects soil gross N transformations and N availability in temperate desert steppes is still limited. Therefore, a ¹⁵N tracing experiment was conducted to study these processes and their underlying mechanism in a desert steppe soil that had been supplemented with N and P for 4 years in northwestern China. Soil N mineralization was increased significantly by P addition, and N and P additions significantly promoted soil autotrophic nitrification, rather than NH₄⁺-N immobilization. The addition of N promoted dissimilatory NO₃⁻ reduction to NH₄⁺, while that of P inhibited it. Soil NO₃⁻-N production was greatly increased by N added alone and by that of N and P combined, while net NH₄⁺-N production was decreased by these treatments. Soil N mineralization was primarily mediated by pH, P content or organic carbon, while soil NH₄⁺-N content regulated autotrophic nitrification mainly, and this process was mainly controlled by ammonia-oxidizing bacteria rather than archaea and comammox. NH₄⁺-N immobilization was mainly affected by functional microorganisms, the abundance of narG gene and comammox Ntsp-amoA. In conclusion, gross N transformations in the temperate desert steppe largely depended on soil inorganic N, P contents and related functional microorganisms. Soil acidification plays a more key role in N mineralization than other environmental factors or functional microorganisms.     

Mechanisms behind the stimulation of nitrification by N input in subtropical acid forest soil

Purpose

Input of N as NH₄ ⁺ is known to stimulate nitrification and to enhance the risk of N losses through NO₃ ^? leaching in humid subtropical soils. However, the mechanisms responsible for this stimulation effect have not been fully addressed.

Materials and methods

In this study, an acid subtropical forest soil amended with urea at rates of 0, 20, 50, 100 mg N kg^?1 was pre-incubated at 25 °C and 60 % water-holding capacity (WHC) for 60 days. Gross N transformation rates were then measured using a ¹⁵N tracing methodology.

Results and discussion

Gross rates of mineralization and nitrification of NH₄ ⁺-N increased (P?<?0.05), while gross rate of NO₃ ^? immobilization significantly decreased with increasing N input rates (P?<?0.001). A significant relationship was established between the gross nitrification rate of NH₄ ⁺ and the gross mineralization rate (R ²?=?0.991, P?<?0.01), so was between net nitrification rate of NH₄ ⁺ and the net mineralization rate (R ²?=?0.973, P?<?0.05).

Conclusions

Stimulation effect of N input on the gross rate of nitrification of NH₄ ⁺-N in the acid soil, partially, resulted from stimulation effect of N input on organic N mineralization, which provides pH-favorable microsites for the nitrification of NH₄ ⁺ in acid soils (De Boer et al., Soil Biol Biochem 20:845–850, 1988; Prosser, Advan Microb Physiol 30:125–181, 1989). The stimulated gross nitrification rate with the decreased gross NO₃ ^? immobilization rate under the elevated N inputs could lead to accumulation of NO₃ ^? and to enhance the risk of NO₃ ^? loss from humid forest soils.

     

Grain legume effects on soil nitrogen mineralization potential and wheat productivity in a Mediterranean environment

The objective of this work was to provide evidence on the effects of faba bean (Vicia faba L.) and chickpea (Cicer arietinum L.) on the dynamics of soil N availability and yield parameters of wheat (Triticum turgidum L. var. durum) in a legume–wheat rotation in comparison with the effects of the more extensively studied common vetch (Vicia sativa L.). Soil samples were taken from field plots just before wheat sowing and incubated in the laboratory to assess N mineralization potential, soil respiration and N immobilization after incorporation of legume residues. Soil after vetch cultivation showed the highest residual N and mineralization potential (120 mg N kg^?1 soil), the greatest CO₂ release and the smallest N immobilization. Smaller mineral N release (80 mg N kg^?1 soil) was shown by soil after faba bean cultivation, which, however, would be capable to support an average wheat production without fertilization. Soil after chickpea and wheat cultivation manifested no differences in residual N and mineralization or immobilization potential. Laboratory results were well correlated with grain yield and N uptake during the second season of rotation in the field. All legumes resulted in significant yield surpluses and provided N credit to the following unfertilized wheat.     

A field study of gross rates of N mineralization and nitrification and their relationships to microbial biomass and enzyme activities in soils treated with dairy effluent and ammonium fertilizer

Abstract. Gross N mineralization and nitrification rates were measured in soils treated with dairy shed effluent (DSE) (i.e. effluent from the dairy milking shed, comprising dung, urine and water) or ammonium fertilizer (NH₄Cl) under field conditions, by injecting ¹⁵N-solution into intact soil cores. The relationships between gross mineralization rate, microbial biomass C and N and extracellular enzyme activities (protease, deaminase and urease) as affected by the application of DSE and NH₄Cl were also determined. During the first 16 days, gross mineralization rate in the DSE treated soil (4.3–6.1 μg N g^?1 soil day^?1) were significantly (P 14;< 14;0.05) higher than those in the NH₄Cl treated soil (2.6–3.4 μg N g^?1 soil day^?1). The higher mineralization rate was probably due to the presence of readily mineralizable organic substrates in the DSE, accompanied by stimulated microbial and extracellular enzyme activities. The stable organic N compounds in the DSE were slow to mineralize and contributed little to the mineral N pool during the period of the experiment. Nitrification rates during the first 16 days were higher in the NH₄Cl treated soil (1.7–1.2 μg N g^?1 soil day^?1) compared to the DSE treated soil (0.97–1.5 μg N g^?1 soil day^?1). Soil microbial biomass C and N and extracellular enzyme activities (protease, deaminase and urease) increased after the application of the DSE due to the organic substrates and nutrients applied, but declined with time, probably because of the exhaustion of the readily available substrates. The NH₄Cl application did not result in any significant increases in microbial biomass C, protease or urease activities due to the lack of carbonaceous materials in the ammonium fertilizer. However, it did increase microbial biomass N and deaminase activity. Significant positive correlations were found between gross N mineralization rate and soil microbial biomass, protease, deaminase and urease activities. Nitrification rate was significantly correlated to biomass N but not to the microbial biomass C or the enzyme activities. Stepwise regression analysis showed that the variations of gross N mineralization rate was best described by the microbial biomass C and N.     

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.

     

Nitrogen Mineralization of Two Manures as Influenced by Contrasting Application Methods under Laboratory Conditions

The decomposition and the associated nitrogen (N) dynamics of organic N sources are affected by their contact with soil. While several authors have examined the effect of surface application or incorporation of crop residues on their decomposition rate, less information is available about the relationship between the placement of animal manure and their N mineralization rate. This study investigated the influence of chicken manure and cattle manure placement on soil N mineralization. The manures were incorporated or surface applied at 175 mg N kg^?1, and N release was periodically determined over 56 days by measuring inorganic N [nitrate (NO₃ ^?) N and ammonium (NH₄ ⁺) N] in a 2 M potassium chloride (KCl) extract at a ratio of 1:10 (w/v). Results indicated that the control soil released a maximum of 64 mg N kg^?1 soil at day 21, a sixfold increase over the initial concentration, which indicates its substantial mineralization potential. Manure treatments showed an initial increase in net NO₃ ^?-N content at the start of the experiments (until day 7) before an extended period of immobilization, which ended at day 21 of the incubation. A small but positive net N mineralization of all manures was observed from 28 days of incubation. At each sampling time, the mean mineral N released from the control was significantly less (P < 0.01) than surface-applied chicken manure, incorporated chicken manure, and surface-applied cattle manure. Treatments exceptions were at days 21 and 28 where N immobilization was at its peak. In contrast, incorporation of cattle manure showed a different N-release pattern, whereby the mineral N amount was only significantly greater than the control soil at days 42 and 56 with 84 and 108 mg N kg^?1 soil respectively. Incorporation of chicken manure and cattle manure did not favor nitrification as much as surface application and cattle manure caused a much greater immobilization when incorporated than when surface applied.     

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.     

Temporal variations of crop residue effects on soil N transformation depend on soil properties as well as residue qualities

Purple soils (Eutric Regosols) are widely distributed in humid subtropical Southwest China. They are characterized by high nitrification activities, with risks of severe NO₃^? leaching. Incorporation of crop residues is considered an effective method to reduce NO₃^? loss. In the present study, we compared the effects of alfalfa, rice straw, and sugarcane bagasse on gross N transformation turnover in a purple soil (purple soil, pH 7.62) compared with those in an acid soil (acid soil, pH 5.26), at 12 h, 3 months, and 6 months after residue incorporation. The gross N transformation rates were determined by ¹⁵N tracing. All tested crop residues stimulated the gross N mineralization rates, but reduced the net mineralization rates in both soils at 12 h after residue incorporation; however, the extent of the effect varied with the crop residue qualities, with rice straw having the strongest effects. Crop residues reduced net nitrification rates by depressing gross autotrophic nitrification rates and stimulating NO₃^? immobilization rates in the purple soil, particularly after rice straw incorporation (net nitrification rate decreased from 16.72 mg N kg^?1 d^?1 in the control to ??29.42 mg N kg^?1 d^?1 at 12 h of residue incorporation); however, crop residues did not affect the gross autotrophic nitrification rates in the acid soil. Crop residue effects subsided almost completely within 6 months, with sugarcane bagasse showing the longest lasting effects. The results indicated that crop residues affected the N transformation rates in a temporal manner, dependent on soil properties and residue qualities.     

Effects of soil moisture on gross N transformations and N2O emission in acid subtropical forest soils

Soil moisture changes, arising from seasonal variation or from global climate changes, could influence soil nitrogen (N) transformation rates and N availability in unfertilized subtropical forests. A ¹⁵?N dilution study was carried out to investigate the effects of soil moisture change (30–90 % water-holding capacity (WHC)) on potential gross N transformation rates and N₂O and NO emissions in two contrasting (broad-leaved vs. coniferous) subtropical forest soils. Gross N mineralization rates were more sensitive to soil moisture change than gross NH₄ ⁺ immobilization rates for both forest soils. Gross nitrification rates gradually increased with increasing soil moisture in both forest soils. Thus, enhanced N availability at higher soil moisture values was attributed to increasing gross N mineralization and nitrification rates over the immobilization rate. The natural N enrichment in humid subtropical forest soils may partially be due to fast N mineralization and nitrification under relatively higher soil moisture. In broad-leaved forest soil, the high N₂O and NO emissions occurred at 30 % WHC, while the reverse was true in coniferous forest soil. Therefore, we propose that there are different mechanisms regulating N₂O and NO emissions between broad-leaved and coniferous forest soils. In coniferous forest soil, nitrification may be the primary process responsible for N₂O and NO emissions, while in broad-leaved forest soil, N₂O and NO emissions may originate from the denitrification process.     

Effects of nickel addition on nitrogen mineralization,nitrification, and nitrogen leaching in some boreal forest soils

The effects of Ni additions on nitrification, N mineralization, and N leaching were examined in soils from boreal jack pine (Pinus banksiana Lamb.) forests. The results of a series of incubation experiments suggested that under certain conditions, Ni at 100 μg g^?1 soil can stimulate nitrification, and at 500 μg g^?1 can stimulate N mineralization. Nitrification rates were very low overall, but were higher in soils from the vicinity of the Sudbury, Ontario Ni-Cu smelters than in uncontaminated soils. The nitrifier populations, estimated by the most probable number method, were extremely low in uncontaminated soils, but also increased following some Ni additions. Increased leaching of NO_f3 ^p was observed in soil columns treated with Ni. Since N tends to be in low supply in boreal forests, and therefore tightly cycled, the observed disruptions caused by Ni inputs could have an effect on forest productivity.     

Effects of long‐term repeated mineral and organic fertilizer applications on soil nitrogen transformations

Repeated applications of mineral and/or organic fertilizer will probably affect gross nitrogen (N) dynamics in soils in the long term but only a limited number of observations are available. Here we present results of a ¹⁵N tracing study with soil from the various fertilizer treatments of the Huang‐Huai‐Hai Plain experiment that has been in operation for more than 17 years. Mineral fertilizer in various combinations of N, phosphorus (P) and potassium (K), organic manure (OM) or a mixture of mineral fertilizer and manure had been repeatedly applied for 17 years. The gross N transformation rates were quantified with a ¹⁵N tracing model, which uses a parameter optimization routine based on Bayesian principles. Mineralization of soil organic matter was at least 2.7 times greater in all fertilizer treatments compared with the untreated control (0.67 µg N g^?1 day^?1). While application of mineral N enhanced mineralization from recalcitrant organic N, the application of organic fertilizers stimulated the mineralization of labile organic N. Gross nitrate (NO₃^?) production solely resulted from ammonium (NH₄⁺) oxidation. Compared with the gross NO₃^? production in the control treatment (2.22 µg N g^?1 day^?1), long‐term N applications stimulated gross nitrification by more than 5.3 times. The largest gaseous N emissions were associated with the organic manure treatments. The ratio of gross NO₃^? production to total mineral N consumption, a ratio proposed previously to determine potential NO₃^? loss, was a good indicator except for the treatment without N application. This ratio increased from 0.8 in the control to 2.7 in the mixture of mineral fertilizer and manure treatment. The largest gaseous N emissions (N₂O + NO) (P < 0.05) were generally found at greater ratios. Results clearly showed that various fertilizers have a differential effect on N dynamics and potential gaseous N losses in the long term.     

Gross nitrogen mineralization-, immobilization-, and nitrification rates as a function of soil C/N ratio and microbial activity

A laboratory experiment was designed to challenge the idea that the C/N ratio of forest soils may control gross N immobilization, mineralization, and nitrification rates. Soils were collected from three deciduous forests sites varying in C/N ratio between 15 and 27. They were air-dried and rewetted to induce a burst of microbial activity. The N transformation rates were calculated from an isotope dilution and enrichment procedure, in which ¹⁵NH₄Cl or Na¹⁵NO₃ was repeatedly added to the soils during 7 days of incubation. The experiments suggested that differences in gross nitrogen immobilization and mineralization rates between the soils were more related to the respiration rate and ATP content than to the C/N ratio. Peaks of respiration and ATP content were followed by high rates of mineralization and immobilization, with 1-2 days of delay. The gross immobilization of NH₄⁺ was dependent on the gross mineralization and one to two orders of magnitude larger than the gross NO₃⁻ immobilization. The gross nitrification rates were negatively related to the ATP content and the C/N ratio and greatly exceeding the net nitrification rates. Taken together, the observations suggest that leaching of nitrate from forest soils may be largely dependent on the density and activity of the microbial community.     

Combining field incubation with nitrogen-15 labelling to examine nitrogen transformations in low to high intensity grassland management systems

 The ¹⁵N isotope dilution method was combined with a field incubation technique to provide simultaneous measurements of gross and net rates of N turnover in three long-term swards: unfertilized (Z) or receiving N either from N fixation as clover (C), or as 200 kg fertilizer N ha^–1 year^–1 (F). Uniform N enrichment of soil microplots was achieved with a multi-point soil injector to measure mineralization/immobilization turnover and nitrification over a 4-day incubation. Net rates of mineralization ranged between 0.6 and 2.9 μg N g^–1 day^–1 and in all three treatments were approximately half the gross rates. Nitrification rates (gross) were between 1.0 and 1.6 μg N g^–1 day^–1. In the F treatment, the turnover of NH₄ ⁺-N and NO₃ ^–-N pools was on a 2- and 4-day cycle, respectively, whereas in the N-limited treatments (C and Z) turnover rates were faster, with the NO₃ ^–-N pools turning over twice as fast as the NH₄ ⁺-N pools. Therefore, available N was recycled more efficiently in the C and Z treatments, whereas in the F treatment a higher N pool size was maintained which would be more vulnerable to leakage. A large proportion of the added ¹⁵N was recovered in the soil microbial biomass (SMB), which represented a 4–5 times larger sink for N than the plant biomass. Although the C treatment had a significantly lower SMB than the grass-only treatments, there were no differences in microbial activity. Gross rates of nitrification increased along the gradient of N input intensity (i.e. Z<C<F), and the addition of a nitrification inhibitor (C₂H₂) tended to increase microbial immobilization, but did not influence plant N uptake. In this study, the value of combining different techniques to verify net rates was demonstrated and the improved methodology for ¹⁵N labelling of soil enabled measurements to be obtained from relatively undisturbed soil under natural field conditions. Received: 25 May 1999