Interactions between fertilizer nitrogen and soil nitrogen—the so-called 'priming' effect

Experiments with ¹⁵N labelled fertilizers often show that plants given fertilizer N take up more N from the soil than plants not given N—the priming effect or ‘added nitrogen interaction’(ANI). This paper is a theoretical study of ANIs and how they can affect the interpretation of experiments with ¹⁵N labelled fertilizers. ANIs can be ‘Real’, if for example, fertilizer N increases the volume of soil explored by roots, or ‘apparent’, caused by pool substitution or by isotope displacement reactions. Pool substitution is the process by which added labelled N stands proxy for native unlabelled N that would otherwise have been removed from that pool. Microbial immobilization of N, whether driven by the decomposition of soil organic matter or by the decomposition of plant roots, can lead to pool substitution and is the dominant cause of apparent ANIs. Denitrification and plant uptake of N can also, under special circumstances, lead to pool substitution and thus give rise to apparent ANIs. Isotope displacement reactions, in which the added labelled N displaces native unlabelled N from a ‘bound’ pool, can lead to apparent ANIs but are only likely to be of significance in exceptional circumstances. The relationship between ANIs, ‘A’ values and N fertilizer uptake efficiencies are examined by means of a simple model for uptake of ¹⁵N-labelled fertilizer by a crop. A positive ‘apparent’ ANI is accompanied by an ‘A’ value that changes as fertilizer applications increase. Likewise, a positive ‘apparent’ ANI also causes fertilizer uptake efficiency to appear lower when measured by the uptake of ¹⁵N than when measured by the non-isotopic ‘difference’ method.     

Mineralization of soil organic nitrogen solubilized by aqua ammonia fertilizer

Organic N solubilized by NH_3(aq) was extracted from ¹⁵N-labelled or unlabelled soil, concentrated and added to non-extracted soil, which was incubated under aerobic conditions at 27±1°C. Gross N mineralization, gross N immobilization, and nitrification in soils with or without addition of unlabelled soluble organic N were estimated by models based on the dilution of the NH ₄ ⁺ or NO _inf3 ^sup- pools, which were labelled with ¹⁵N at the beginning of incubation. Mineralization of labelled organic N was measured by the appearance of label in the mineral N pool. Although gross N mineralization and gross N immobilization were increased in two soils between day 0 and day 7 following addition of unlabelled organic N solubilized by NH_3(aq), there was no increase in net N mineralization. Solubilization of ¹⁵N-labelled organic N increased and the ¹⁵N enrichment of the soluble organic N decereased as the concentration of NH_3(aq) added increased. A constant proportion of approximately one-quarter of the labelled organic N added at different rates to non-extracted soil was recovered in the mineral N pool after an incubation period of 14 days, and the availability ratios calculated from net N mineralization data were 1.1:1 and 2.1:1 for 111 and 186 mg added organic-N kg^-1 soil, respectively, indicating that the mineralization of organic N was increased by solubilization.     

Uptake of soil nitrogen by soybean as influenced by symbiotic N2-fixation or fertilizer nitrogen supply

Nodulated and N₂-fixing soybean plants (Glycine max. L.) grown in a pot experiment took up significantly more soil N (labelled with ¹⁵N) than non-nodulated control plants. The organic matter in the experimental soil was labelled with ₁₅N during a previous incubation, and the pool of labelled inorganic N originated mainly from mineralization of organic matter. Addition of non-labelled ammonium or nitrate-N to non-nodulated plants did not increase their uptake of labelled soil N. Plants grown with the various N-sources exhausted the soil for KCl-extractable N to almost the same low concentration. Where non-nodulated plants were grown, 60–75% of the inorganic N initially present could be accounted for in plants and KCl-extracts at harvest. An amount corresponding to 98% of the KCl-extractable N initially present was found in nodulated plants and the pool of KCl-extractable N.     

Predictors of gross N mineralization and immobilization during decomposition of stabilized organic matter in agricultural soil

Long-term additions of different types of organic amendments affect the amount of soil organic matter. Less is known about how this in turn affects carbon (C) and nitrogen (N) mineralization from the pool of stabilized soil organic matter, or the extent to which gross N immobilization influences the net amount of N mineralized. Soils, differing in the quantity and quality of organic matter inputs they had received since 1956, were sampled approximately 6 or 18 months after the most recent applications of organic amendments. Two laboratory experiments were carried out to: (i) evaluate if, and how, the organic amendments had affected C mineralization, gross and net N mineralization; (ii) examine the relation between gross N immobilized and free-light fraction of organic matter; and (iii) assess predictors for gross N mineralization and immobilization rates in soils. The amount of soil organic C and N were major determinants of C and gross N mineralization, but not of net N mineralization. Carbon mineralization was related to gross N mineralization, but the ratio between the two was not constant. Gross N immobilization was related to the amount of free-light fraction material in the soil with 90% variation explained. For most common organic amendments applied in autumn, our results support the use of total soil organic N and C mineralization as predictors of gross N mineralization from stabilized soil organic matter. In addition, we propose that the amount of free-light fraction material present in the soil in spring is adequate as a predictor of the immobilization potential of the soil, without a need to consider the C-to-N ratio of this material.     

Fate and interaction with native soil N of ammonium N applied to wetland rice (Oryza sativa L.) grown under saline and non-saline conditions

Summary The effect of salts on the balance of fertilizer N applied as ¹⁵N-labelled ammonium sulphate and its interaction with native soil N was studied in a pot experiment using rice (Oryza sativa L.) as a test crop. The rice crop used 26%–40% of the applied N, the level of applied N and salts showing no significant bearing on the uptake of fertilizer N. Losses of fertilizer N ranged between 54% and 68% and only 5%–8% of the N was immobilized in soil organic matter. Neither the salts nor the rate of N application had any significant effect on fertilizer N immobilization. The effective use of fertilizer N (fertilizer N in grain/fertilizer N in whole plant) was, however, better in the non-saline soil. The uptake of unlabelled N (N mineralized from soil organic matter and that originating from biological N₂ fixation in thes rhizosphere) was inhibited in the presence of the salts. However, in fertilized soil, the uptake of unlabelled N was significantly enhanced, leading to increased A values [(1-% Ndff/% Ndff)x N fertilizer applied, where Ndff is N derived from fertilizer], an index of interaction with the added N. This added N interaction increased with increasing levels of added N. Since the extra unlabelled N taken up by fertilized plants was greater than the fertilizer N immobilized, and the root biomass increased with increasing levels of added N, a greater part of the added N interaction was considered to be real, any contribution by an apparent N interaction (pool substitution or isotopic displacement) to the total calculated N interaction being fairly small. Under saline conditions, for the same level of fertilizer N addition, the added N interaction was lower, and this was attributed to a lower level of microbial activity, including mineralization of native soil N, rootdriven immobilization of applied N, and N₂ fixation.     

施入~(15)N标记氮肥在长期不同培肥土壤的残留及其利用

采用盆栽试验和短期矿化培养相结合的方法,研究了施入15N标记氮肥(+N)及其与秸秆配施(+1/2N+1/2S)在3种长期(19年)不同培肥土壤(即:No-F,长期不施肥土壤;NPK,长期施用NPK化肥土壤;MNPK,长期有机无机肥配施土壤)中的残留及其矿化和作物吸收特性。结果表明,第一季小麦收获后,+1/2N+1/2S处理下三供试土壤和+N处理下的NPK和MNPK土壤残留肥料氮(残留15N)中有82.6%~95.1%以有机态存,而+N处理下No-F土壤残留15N有47.7%以矿质态存在。经过28 d矿化培养后,与NPK土壤相比,MNPK土壤氮素净矿化量显著增加,增幅为39%~49%;NPK和MNPK土壤残留肥料氮(残留15N)矿化量为1.23~1.90 mg kg-1,占总残留15N的2.78%~5.53%,均显著高于No-F土壤。与+N处理相比,+1/2N+1/2S处理显著提高了3供试土壤氮素净矿化量,但两施肥处理对NPK和MNPK土壤残留15N矿化量无显著影响。+N处理下No-F土壤残留15N的利用率为20%,显著高于NPK(9%)和MNPK(12%)土壤。两种施肥处理下,MNPK土壤残留15N的利用率均显著高于NPK土壤。短期培养期间土壤氮素矿化量和第二季小麦生育期作物吸氮量呈显著性正相关,而残留15N矿化量和第二季小麦吸收残留15N量间无显著性相关关系。长期有机无机配施可以提高土壤残留肥料氮的矿化量及有效性。     

Effect of acetylene provided by wax-coated calcium carbide on transformations of urea nitrogen applied to an irrigated wheat crop

The effect of acetylene (provided by wax-coated calcium carbide, CaC₂) on N transformations in a red-brown earth was measured in a field experiment with irrigated wheat by determining the change in the concentration and ¹⁵N enrichment of the organic N and mineral N pools with time. The study was conducted in the Goulburn-Murray Irrigation region of south-eastern Australia using 0.3 m by 0.3 m microplots fertilized with ¹⁵N-labelled urea (10 g N m^-2; 5 atom% ¹⁵N). Acetylene was effective in slowing the nitrification of both unlabelled and labelled N. Nitrate derived from the added fertilizer reached a maximum 19 days after sowing in the treatment without CaC₂, whereas little nitrate accumulated in the 8 g CaC₂ m^-2 treatment. There was significant immobilization of the urea N by 19 days after sowing in all treatments, but the extent of immobilization was not affected by the acetylene. The addition of acetylene slowed net mineralization of labelled and unlabelled N from the organic N pool, and resulted in increased accumulation of both unlabelled and labelled N in wheat tops.     

Modelling the turnover of 15N-labelled fertilizer and cover crop in soil and its recovery by maize

The rate at which available nitrogen (N) is released from organic materials in soil is often measured by applying ¹⁵N and following its recovery by the growing crop. However, the turnover of labelled N in soil modifies the ratio of labelled to unlabelled available N and thereby affects the uptake of ¹⁵N by plants. The recovery of labelled N by maize was measured in a field experiment under three management systems, with one ¹⁵N‐labelled input in each: (1) conventional, with fertilizer side dressing, (2) low input, with vetch as a cover crop and fertilizer side dressing, and (3) organic, with vetch and composted manure. The NCSOIL model, which simulates C and N turnover in soil, was modified to include relevant processes related to the maize crop, and used to estimate the decomposition rate constant of vetch in the field by optimizing the simulated dynamics of labelled N uptake by maize against the measured results. A large input of C from mineralizable soil organic matter and root deposition was necessary to account for the recovery of fertilizer N by maize. Optimization of labelled N recovery in the low input system resulted in two optional rate constants for the decomposition of vetch: rapid decomposition (0.4 day^?1) of a labile vetch pool (49% of total vetch N), or slow decomposition (0.008 day^?1) of a single vetch pool. In the simulated organic system, where manure and vetch were incorporated at the same time, only a rapid decomposition of the labile component of vetch accounted well for the recovery of vetch N by maize. The prolonged recycling of N mineralized from the vetch, and its mixing with fertilizer side dressing in the low input system, reduced the recovery of vetch N even though it was mineralized rapidly. This demonstrates the difficulty in assessing the availability of N from organic materials.     

Effects of 15N-labelled ammonium nitrate and urea on soil nitrogen during growth of wheat (Triticum aestivum L.) under field conditions

We studied the effects of ¹⁵N-labelled ammonium nitrate and urea on the yield and uptake of labelled and unlabelled N by wheat (Triticum aestivum L., cv. Mexi-Pak-65) in a field experiment. The dry matter and N yields were significantly increased with fertilizer N application compared to those from unfertilized soil. The wheat crop used 33.6–51.5 and 30.5–40.9% of the N from ammonium nitrate and urea, respectively. Splitting the fertilizer N application had a significant effect on the uptake of fertilizer N by the wheat. The fertilizer N uptake showed that ammonium nitrate was a more available source of N for wheat than urea. The effective use of fertilizer N (ratio of fertilizer N in grain to fertilizer N in whole plant) was statistically similar for the two N fertilizers. The application of fertilizer N increased the uptake of unlabelled soil N by wheat, a result attributed to a positive added N interaction, which varied according to the fertilizer N split; six split applications gave the highest added N interaction compared to a single application or two split applications for both fertilizers. Ammonium nitrate gave 90.5, 33.5, and 48.5% more added N interaction than urea with one, two, and six split N applications. A values were not significantly correlated with the added N interaction (r=0.557). The observed added N interaction may have been the result of pool substitution, whereby added labelled fertilizer N replaced unlabelled soil N.     

Mineralization and microbial immobilization of N and P in arctic soils in relation to season,temperature and nutrient amendment

In situ summer, winter and annual net N and P mineralization and microbial immobilization of mineralized nutrients were measured in a low-altitude subarctic/alpine dwarf shrub heath and in a high-altitude fellfield. Net mineralization was determined by using the buried-bag technique, which was combined with fumigation–extraction to recover microbial nutrients and estimate microbial nutrient immobilization. The measurements were carried out in unperturbed plots and in plots, which had been subjected to elevated temperature and fertilizer addition for 5 years before the experiment started. During the growing season, the microbes in the unperturbed plots immobilized the major part of the mineralized nutrients, which resulted in low net mineralization. This occurred also during winter, when we assumed that nutrients should be released during microbial die-back. However, we found no evidence for a large microbial winter die-back and the surviving microbial biomass even immobilized extra nutrients.Soil temperature enhancement by ca. 2°C in general increased, or tended to increase, net mineralization. However, there was not necessarily any strong correlation between net mineralization and temperature because temperature-induced increase in gross mineralized nutrients could either lead to nutrient immobilization in the microbes or the nutrients could be released to the soil inorganic pool.Fertilizer additions had no major effect on net nutrient mineralization or nutrient immobilization. However, the ligno-cellulose index, which has been used as a predictor of substrate quality and usually correlates negatively with decomposition rate, also appeared to be a good predictor of gross mineralization, but a poor predictor of net mineralization.     

Interaction of 15N-labelled ammonium nitrate,urea and ammonium sulphate with soil N during growth of wheat (Triticum aestivum L.) under field conditions

The effects of ¹⁵N-labelled ammonium nitrate, urea and ammonium sulphate on yield and uptake of labelled and unlabelled N by wheat (Triticum aestivum L. cv. Mexi-Pak-65) were studied in a field experiment. The dry matter and N yields were significantly increased with fertilizer N application compared to those from unfertilized soil. The wheat crop used 64.0–74.8%, 61.5–64.7% and 61.7–63.4% of the N from ammonium nitrate, urea and ammonium sulphate, respectively. The fertilizer N uptake showed that ammonium nitrate was a more available source of N for wheat than urea and ammonium sulphate. The effective use of fertilizer N (ratio of fertilizer N in grain to fertilizer N in whole plant) was statistically similar for the three N fertilizers. The application of fertilizer N increased the uptake of unlabelled soil N by wheat, a result attributed to a positive added N interaction, which varied with the method of application of fertilizer N. Ammonium nitrate, urea and ammonium sulphate gave 59.3%, 42.8% and 26.3% more added N interaction, respectively, when applied by the broadcast/worked-in method than with band placement. A highly significant correlation between soil N and grain yield, dry matter and added N interaction showed that soil N was more important than fertilizer N in wheat production. A values were not significantly correlated with added N interaction (r=0.719). The observed added N interaction may have been the result of pool substitution, whereby added labelled fertilizer N stood proxy for unlabelled soil N.     

Contributions to N mineralization from soil macroorganic matter fractions incorporated into two field soils

The contribution of soil macroorganic matter N (macro-OM, d < 1.0 g cm⁻³) to gross rates of N mineralization was examined in two grassland field soils in England using three ¹⁵N-labelling techniques, referred to as the difference, mirror image and net recovery methods. The difference method involved measuring gross mineralization rates in soils with or without incorporated unlabelled macro-OM, using isotope dilution of added ¹⁵NH₄⁺. The mirror image approach involved measuring the isotopic enrichment of the ammonium pool in soil to which ¹⁵N-labelled macro-OM had been incorporated. The net recovery method was a net N mineralization estimate based upon the recovery of label in plants and soil to which ¹⁵N-labelled macro-OM had been incororated. The difference method provided the most accurate estimates of N mineralization from the incorporated macro-OM. Estimates made using the direct and net recovery methods were more variable and confounded by movement of the macro-OM away from the original site of incorporation. Approximately 2.4 and 13.7% of the N in the incorporated macro-OM isolated from the different soils was mineralized over the 66 d following incorporation. This represented approximately 3.4 and 2.3% of the cumulative gross N mineralization when corrected for background amounts of soil macro-OM. This low contribution suggests that most of the N mineralized in grazed grasslands is derived from other forms of soil organic matter associated with mineral particles.     

Mineralization and immobilization of nitrogen in fumigated soil and the measurement of microbial biomass nitrogen

Immobilization of N was measured in a fumigated and in an unfumigated soil by adding (¹⁵NH₄)₂SO₄ and following the disappearance of inorganic label from the soil solution and its simultaneous conversion to soil organic N. Calculations based on the measurement of organically-bound ¹⁵N gave more consistent values for immobilization than did calculations based on the measurement of the disappearance of label from solution. The fumigated soil immobilized 6.6 μg N g^?1 N g^?1 soil in 10 days at 25°C, the unfumigated control 4.8 μg. The corresponding gross mineralization rates were 34.9 and 5.6 μg N g^?1 soil in 10 days.Addition of 58 μg N as (¹⁵NH₄)₂SO₄ to the fumigated soil increased the quantity of the ynlabelled NH₄-N extracted at the end of 10 days from 33.8 to 37.8 μg Ng^?1 soil, i.e. there was a positive Added Nitrogen Interaction (ANI). The added labelled N produced this ANI, not by increasing the rate of mineralization of organic N, but by standing proxy for unlabelled N that otherwise would have been immobilized.A procedure for calculating biomass N from the size of the flush of mineral N caused by fumigation is proposed. Biomass N (B_N) is calculated from the relationship B_N = F'_N/0.68 where F'_N is [(N in fumigated soil incubated for 10 days — (N in unfumigated soil incubated for 10 days)].     

Effect of increasing rates of 15N‐labelled fertilizer on recovery of fertilizer N in plant and soil N pools in a pot experiment with winter wheat

The effect of increasing rates of ¹⁵N‐labelled Ca(NO₃)₂ (N₀ = no N application, N₃₀₀ = 300 mg N/pot; N₆₀₀ = 600 mg N/pot; N₉₀₀ = 900 mg N/pot) on recovery of fertilizer N in winter wheat plants and soil (total soil N, soil microbial biomass N [N_mic], extractable organic N [N_org]) and on N mineralization (NM_soil) was investigated at milk‐ripe growth stage in a pot experiment. The N rates were equally split at tillering, stem elongation and ear emergence. Fertilizer N recovered in crops increased with increasing N rates (N₃₀₀: 223.5 mg N/pot [74.5% of applied fertilizer N], N₆₀₀: 445.6 mg N/pot [74.3%], N₉₀₀: 722.1 mg N/pot [80.2%]). NM_soil slightly increased from N₀ (43.8 mg N/pot) to N₉₀₀ (75.6 mg N/pot) indicating that N application enhanced availability of soil‐derived N for the plants. However, in fertilized treatments NM_soil is balanced by immobilization and losses (non‐recovered fertilizer N). Therefore the effective soil N mineralization is indicated by apparent net N mineralization (ANNM = NM_soil — fertilizer N immobilization — lost fertilizer N). Fertilizer N immobilization in soil increased from N₃₀₀ (38.7 mg N/pot) to N₆₀₀ (60.7 mg N/pot) and N₉₀₀ (65.5 mg N/pot). Lost fertilizer N increased from N₃₀₀ (14.8 mg N/pot) to N₆₀₀ (56.7 mg N/pot) and N₉₀₀ (62.1 mg N/pot). As a consequence negative ANNM values were calculated at N₆₀₀ and N₉₀₀. Due to the small differences between N₆₀₀ and N₉₀₀ fertilizer N immobilization and lost fertilizer N did not increase linearly with increasing N rates, i.e. both processes were limited by factors other than N rate. Only 5.6—7.4% of the immobilized fertilizer N was recovered in N_org and 5.4—9.3% in N_mic soil pools. It is assumed that most of the immobilized fertilizer N was in non‐extractable organic N forms. N_mic and N_org were weak indicators for the extent of fertilizer N immobilization.     

Transformations of nitrogen fertilizers in soil

The effects of ¹⁵N-labelled urea, (NH₄)₂SO₄ and KNO₃ on immobilization, mineralization, nitrification and ammonium fixation were examined under aerobic conditions in an acid tropical soil (pH 4.0) and in a neutral temperate soil (pH 6.8). Urea, (NH₄)₂SO₄ and KNO₃ slightly increased net mineralization of soil organic nitrogen in both soils. There was also an apparent Added Nitrogen Interaction (ANI) i.e. added labelled NH₄-N stood proxy for unlabelled NH₄-N that would otherwise have been immobilized. So far as immobilization and nitrification were concerned, urea and (NH₄)₂SO₄ behaved very similarly in each soil. Immobilization of NO₃-N was negligible in both soils. Some of the added labelled NH₄-N was rapidly fixed, more by the temperate soil than by the tropical soil. This labelled fixed NH₄-N decreased during incubation, in contrast to labelled organic N, which did not decline.     

Seasonal dynamics of carbon and nitrogen pools and fluxes under continuous arable and ley-arable rotations in a temperate environment

Improved understanding of the seasonal dynamics of C and N cycling in soils, and the main controls on these fluctuations, is needed to improve management strategies and to better match soil N supply to crop N demand. Although the C and N cycles in soil are usually considered to be closely linked, few data exist where both C and N pools and gross N fluxes have been measured seasonally. Here we present measurements of inorganic N, extracted soluble organic N, microbial biomass C and N, gross N fluxes and CO₂ production from soil collected under wheat in a ley‐arable and continuous arable rotation within a long‐term experiment. The amounts of inorganic N and extracted soluble organic N were similar (range 5–35 kg N ha⁻¹; 0–23 cm) but had different seasonal patterns: whilst inorganic N declined during wheat growth, extracted soluble organic N peaked after cultivation and also during maximal stem elongation. The microbial biomass was significantly larger in the ley‐arable (964 kg C ha⁻¹; 0–23 cm) than the continuous arable rotation (518 kg C ha⁻¹; 0–23 cm) but with no clear seasonal pattern. In contrast, CO₂ produced from soil and gross N mineralization showed strong seasonality linked to soil temperature and moisture content. Normalization of soil CO₂ production and gross N mineralization with respect to these environmental regulators enabled us to study the underlying influence of the incorporation of fresh plant material into soil on these processes. The average normalized gross rates of N mineralized during the growing season were 1.74 and 2.55 kg N ha⁻¹ nday⁻¹ in continuous arable and ley‐arable rotations respectively. Production rates (gross N mineralization, gross nitrification) were similar in both land uses and matched rates of NH₄⁺ and NO₃⁻ consumption, resulting in periods of net N mineralization and immobilization. There was no simple relationship between soil CO₂ production and gross N mineralization, which we attributed to changes in the C : N ratio of the mineralizing pool(s).     

Priming effects of 15N-labelled ammonium nitrate on uptake of soil N by wheat (Triticum aestivum L.) under field conditions

Summary The uptake of labelled and unlabelled N by wheat was measured in a field experiment using ¹⁵N-labelled ammonium nitrate fertilizer. The dry matter yield and N yields were significantly increased with fertilizer N application compared to those from unfertilized soil. The uptake of applied N by wheat ranged between 25 and 34%. Fertilizer N application increased the uptake of unlabelled soil N which was attributed to a positive priming effect or added N interaction. The added N interaction observed by applying 20, 60, and 120 kg fertilizer N was 11.4, 19.1, and 27.9 kg, corresponding to 26, 44 and 64%, respectively of the N taken up from unfertilized soil. The A values did not alter with the increase in fertilizer N application. The observed added N interaction may have been the result of pool substitution whereby added labelled fertilizer N stood proxy for unlabelled soil N. A significant correlation coefficient (r=0.996^**) between the uptake of soil N and the dry matter yield showed that soil N was more important than fertilizer N in wheat production.     

Long-term organic phosphorus mineralization in Spodosols under forests and its relation to carbon and nitrogen mineralization

In forest soils where a large fraction of total phosphorus (P) is in organic forms, soil micro-organisms play a major role in the P cycle and plant availability since they mediate organic P transformations. However, the correct assessment of organic P mineralization is usually a challenging task because mineralized P is rapidly sorbed and most mineralization fluxes are very weak. The objectives of the present work were to quantify in five forest Spodosols at soil depths of 0-15 cm net mineralization of total organic P and the resulting increase in plant available inorganic P and to verify whether net or gross P mineralization could be estimated using the C or N mineralization rates. Net mineralization of total organic P was derived from the net changes in microbial P and gross mineralization of P in dead soil organic matter. We studied very low P-sorbing soils enabling us to use lower extractants to assess the change in total inorganic P as a result of gross mineralization of P in dead soil organic matter. In addition, to enable detection of gross mineralization of P in dead soil organic matter, a long-term incubation (517 days) experiment was carried out. At the beginning of the experiment, total P contents of the soils were very low (19-51 μg g⁻¹) and were essentially present as organic P (17-44 μg g⁻¹, 85-91%) or microbial P (6-14 μg g⁻¹; 24-39%). Conversely, the initial contents of inorganic P were low (2-7 μg g⁻¹; 9-15%). The net changes in the pool size of microbial P during the 517 days of incubation (4-8 μg g⁻¹) and the amounts of P resulting from gross mineralization of dead soil organic matter (0.001-0.018 μg g⁻¹ day⁻¹; 0.4-9.5 μg g⁻¹ for the entire incubation period) were considerable compared to the initial amounts of organic P and also when compared to the initial diffusive iP fraction (<0.3 μg g⁻¹). Diffusive iP corresponds to the phosphate ions that can be transferred from the solid constituents to the soil solution under a gradient of concentration. Net mineralization of organic P induced an important increase in iP in soil solution (0.6-10 μg g⁻¹; 600-5000% increase) and lower increases in diffusive iP fractions (0.3-5 μg g⁻¹; 300-2000% increase), soil solid constituents having an extremely low reactivity relative to iP. Therefore, soil micro-organisms and organic P transformations play a major role in the bioavailability of P in these forest soils. In our study, the dead soil organic matter was defined as a recalcitrant organic fraction. Probably because gross mineralization of P from this recalcitrant organic fraction was mainly driven by the micro-organisms’ needs for energy, the rates of gross mineralization of C, N and P in the recalcitrant organic fraction were similar. Indirect estimation of gross mineralization of P in dead soil organic matter using the gross C mineralization rate seems thus an alternative method for the studied soils. However, additional studies are needed to verify this alternative method in other soils. No relationships were found between microbial P release and microbial C and N releases.     

Nitrogen compounds extracted by electroultrafiltration (EUF) or CaCl2 solution and their relationships to nitrogen mineralization in soils

The objective of the investigation was to identify the most important organic N-containing fractions extracted from soils by electroultrafiltration (EUF) or a CaCl₂ solution, respectively, and their importance for nitrogen mineralization. The investigation comprised 19 agricultural and one forest top soil. Net N mineralization was tested in Mitscherlich pot experiments with three treatments: (1) fallow soil without N fertilizer, (2) soil cultivated with rye grass without N fertilizer, (3) soil cultivated with rye grass with N fertilizer. The highest proportion of N in the extracts was the amino N fraction (amino acids + peptides) amounting to approximately 60% of the total N extracted by CaCl₂ and to about 40% of the total N extracted by EUF. The proportion of amino sugars from total N extracted was in average 10% for the CaCl₂ and 5.2% for the EUF extracts. The proportion of heterocyclic N bases derived from nucleic acids amounted in average to 4.8% and 3.6% for the CaCl₂ and EUF extract, respectively. Amino N (amino acids + peptides) were correlated best with net N mineralization (EUF, r = 0.81***, CaCl₂, r = 0.86***). The correlation between amino sugars and net N mineralization was r = 0.55* for the EUF extract and r = 0.49* for the CaCl₂ extract. The heterocyclic N bases did not correlate with net N mineralization. Correlations between Norg extracted by CaCl₂ versus net N mineralization were higher than those obtained by the EUF extract. Net N mineralization was about four times higher in the fallow soils than in the treatment with grass and no N fertilizer. In the treatment with grass + N fertilizer on average no net N mineralization occurred, moreover there was a tendency of N immobilization. It is assumend that in the treatments with grass cultivation, organic C released by roots stimulated the assimilation of mineral N and amino acids by soil microorganisms resulting in a low net N mineralization. Net N mineralization led to a highly significant depletion in the Norg pools and particularly in the amino N and amino sugar pools in the treatment with grass and without N fertilizer. This depletion was particularly evident in the CaCl₂ extracts. The results justify the conclusion that the Norg obtained with both extraction methods originates from a dynamic N pool into which N flows in and out. The amino N extractable with EUF or CaCl₂ is a reliable indicator for the net N mineralization potential of soils.     

氮肥与有机肥配施对设施土壤净矿化氮动态变化的影响

研究设施栽培条件下氮肥与有机肥配施对土壤净矿化氮含量及其速率的动态变化的影响,以评估净矿化氮在设施土壤供氮能力方面的作用,为设施番茄生产的合理施肥提供重要的理论依据。以设施番茄栽培连续7年定位施肥田间试验为依托,选择不同施氮量（N0、N1、N2、N3）和不同氮量配施有机肥（MN0、MN1、MN2、MN3）8个处理土壤,采用室内连续好氧培养方法,研究了各施肥处理土壤净矿化氮含量及净氮矿化速率,分析了土壤净矿化氮含量与可溶性有机氮、微生物量氮含量之间的联系。研究结果表明:在0 ~ 20 cm土层,氮肥与有机肥配施处理土壤全氮和无机氮含量均显著高于单施氮肥处理（P < 0.05）,施氮量对土壤全氮含量无显著影响,但对土壤无机氮含量则有显著影响,随施氮量的增加呈显著增加趋势。在培养过程中,各处理土壤净矿化氮含量随着培养时间延长呈先逐渐增加而后下降趋势,各处理土壤净氮矿化速率在培养7 d时最大,7 ~ 70 d期间快速下降,70 d后呈缓慢下降趋势,氮肥与有机肥配施处理土壤净矿化氮量和净氮矿化速率均显著高于单施氮肥处理（P < 0.05）,氮肥与有机肥配施处理土壤净矿化氮含量和净氮矿化速率随施氮量增加呈下降趋势;与单施氮肥相比,氮肥与有机肥配施显著提高土壤可溶性有机氮与微生物量氮含量（P < 0.05）,但受施氮量影响不显著;土壤净矿化氮含量与可溶性有机氮、微生物量氮之间有密切联系,但与可溶性有机氮之间的密切程度更大。综合来看,MN1、MN2处理可显著提高土壤供氮能力（无机氮 + 净矿化氮）。在设施番茄栽培条件下,连续7年氮肥与有机肥配施可显著提高设施土壤供氮能力,也可较好地协调设施土壤氮素供应与固持的关系。