Importance of organic nitrogen fractions in sandy soils,obtained by electro-ultrafiltration or CaCl2 extraction,for nitrogen mineralization and nitrogen uptake of rape

Summary Sandy soils have low reserves of mineral N in spring. Therefore organic-bound N is the most important pool available for crops. The objective of the present investigation was to study the importance of the organic-bound N extracted by electro-ultrafiltration and by a CaCl₂ solution for the supply of N to rape and for N mineralization. Mitscherlich-pot experiments carried out with 12 different sandy soils (Germany) showed a highly significant correlation between the organic N extracted (two fractions) and the N uptake by the rape (electroultrafiltration extract: r=0.76^***; CaCl₂ extract: r=0.76^***). Organic N extracted by both methods before the application of N fertilizer was also significantly correlated with N mineralization (electro-ultrafiltration extract: r=0.75^***; CaCl₂ extract: r=0.79^***). N uptake by the rape and the mineralization of organic N increased with soil pH and decreased with an increasing C:N ratio and an increasing proportion of sand in the soils. Ninety-eight percent of the variation in N uptake by the rape was determined by the differences in net mineralization of organic N. This show that in sandy soils with low mineral N reserves (NO _inf3 ^sup- -N, NH ₄ ⁺ -N) the organic soil N extracted by electro-ultrafiltration or CaCl₂ solutions indicates the variance in plant-available N. Total soil N was not related to the N uptake by plants nor to N mineralization.     

The influence of tillage on the proportion of organic carbon and nitrogen in the microbial biomass of medium-textured soils in a humid climate

Summary Microbial biomass C and N respond rapidly to changes in tillage and soil management. The ratio of biomass C to total organic C and the ratio of mineral N flush to total N were determined in the surface layer (0–5 cm) of low-clay (8–10%), fine sandy loam, Podzolic soils subjected to a range of reduced tillage (direct drilling, chisel ploughing, shallow tillage) experiments of 3–5 years' duration. Organic matter dynamics in the tillage experiments were compared to long-term conditions in several grassland sites established on the same soil type for 10–40 years. Microbial biomass C levels in the grassland soils, reduced tillage, and mouldboard ploughing treatments were 561, 250, and 155 g g^-1 soil, respectively. In all the systems, microbial biomass C was related to organic C (r=0.86), while the mineral N flush was related to total N (r=0.84). The average proportion of organic C in the biomass of the reduced tillage soils (1.2) was higher than in the ploughed soils (0.8) but similar to that in the grassland soils (1.3). Reduced tillage increased the average ratio of mineral N flush to total soil N to 1.9, compared to 1.3 in the ploughed soils. The same ratio was 1.8 in the grassland soils. Regression analysis of microbial biomass C and percent organic C in the microbial biomass showed a steeper slope for the tillage soils than the grassland sites, indicating that reduced tillage increased the microbial biomass level per unit soil organic C. The proportion of organic matter in the microbial biomass suggests a shift in organic matter equilibrium in the reduced tillage soils towards a rapid, tillage-induced, accumulation of organic matter in the surface layer.     

Effects of pretreatment of soil samples on N mineralization in incubation experiments

Summary We studied the effects of pretreating soil samples (field-fresh, drying at 40° and 105°C, freezing/thawing) on N mineralization in an incubation experiment and on the dynamics of the organic N fraction extracted by K₂SO₄ solution. The soil samples were collected from plots in a long-term field experiment with the application of mineral fertilizer and farmyard manure. Compared with the field-fresh soil samples, freezing/thawing resulted in higher NO ₃ ^– -N contents while the NH ₄ ⁺ -N and the organic N content were increased by drying at 105°C. During the incubation period N mineralization was highest after the samples were dried at 105°C and a little lower in those dried at 40°C. After freezing/thawing the order of magnitude of N mineralization remained the same. The difference in organic N between the beginning and the end of the incubation experiment and the mineral N content at the end of the experiment were correlated significantly. Despite this correlation, however, the change in the organic N content underestimated the N mineralization rates.     

Sulfur mineralization rates and potentials of soils

Summary Field-moist soil and glass beads mixtures were packed in glass tubes and leached with 100 ml of 5 mM CaCl₂ and incubated at 20 or 30°C. The leaching procedure was repeated every 2 weeks for 14 weeks. The leachates were analysed for SO _inf4 ^sup2– and NO₃ ^–. The S uptake by three successive croppings of corn (Zea mays L.) or soybean [Glycine max (L.) Merr.] at 40- or 60-day intervals, respectively, or three cuttings of ryegrass (Lolium multiflorum L.) at 30-day intervals were studied under greenhouse conditions. Results showed that significantly greater amounts of S were mineralized at 30°C than at 20°C in each of 13 Iowa and 7 Chilean surface soils. Expressed as percentages of organic S in soils, the amounts of S mineralized in the Iowa surface soils in 14 weeks at 20 and 30°C ranged from 1.2% to 9.8% and from 2.4% to 17.5%, respectively. The corresponding values for the Chilean soils ranged from 0.9% to 7.2%6 and from 1.4% to 12.1%. The Q₁₀ values of S mineralization ranged from 1.7 to 4.4 (average 2.5) for the Iowa soils and from 1.7 to 3.1 (average 2.1) for the Chilean soils. The cumulative S mineralized at 20°C in 14 weeks was significantly correlated with the cumulative N mineralized (linear model, r=0.72^**; quadratic model, r=0.84^***). Similarly, the cumulative S mineralized at 30°C was significantly correlated with the cumulative N mineralized at this temperature (linear model, r=0.81^***; quadratic model, r = 0.82^***). The potentially mineralizable S pool (S₀), calculated by using an exponential equation for the S mineralized at 20°C, ranged from 5 to 44 mg kg^–1 for the Iowa soils and from 10 to 25 mg kg^–1 for the Chilean soils. The corresponding values obtained by using a reciprocal-plot technique ranged from 6 to 48 mg kg^–1 and from 12 to 26 mg kg^–1, respectively. The S₀ values calculated for S mineralized at 30°C, in general, were higher than those obtained at 20°C. The S mineralization rate constant (k) and the time required to mineralize 50% of S₀ (K _t), calculated by using the cumulative SO _inf4 ^sup2– released during 14 weeks of incubation, varied considerably among the soils. Up take of S by corn and soybean (tops+roots) were, in general, lower than the total SO _inf4 ^sup2– mineralized in 14 weeks at 20°C.     

Microbial biomass,N mineralization,and the activities of various enzymes in relation to nitrate leaching and root distribution in a slurry-amended grassland

High rates of cattle slurry application induce NO _inf3 ^sup- leaching from grassland soils. Therefore, field and lysimeter trials were conducted at Gumpenstein (Austria) to determine the residual effect of various rates of cattle slurry on microbial biomass, N mineralization, activities of soil enzymes, root densities, and N leaching in a grassland soil profile (Orthic Luvisol, sandy silt, pH 6.6). The cattle slurry applications corresponded to rates of 0, 96, 240, and 480 kg N ha^-1. N leaching was estimated in the lysimeter trial from 1981 to 1991. At a depth of 0.50 m, N leaching was elevated in the plot with the highest slurry application. In October 1991, deeper soil layers (0–10, 10–20, 20–30, 30–40, and 40–50 cm) from control and slurry-amended plots (480 kg N ha^-1) were investigated. Soil biological properties decreased with soil depth. N mineralization, nitrification, and enzymes involved in N cycling (protease, deaminase, and urease) were enhanced significantly (P<0.05) at all soil depths of the slurry-amended grassland. High rates of cattle slurry application reduced the weight of root dry matter and changed the root distribution in the different soil layers. In the slurry-amended plots the roots were mainly located in the topsoil (0–10 cm). As a result of this study, low root densities and high N mineralization rates are held to be the main reasons for NO _inf3 ^sup- leaching after heavy slurry applications on grassland.     

Nitrogen mineralization in relation to site history and soil properties for a range of Australian forest soils

Rates of N mineralization were measured in 27 forest soils encompassing a wide range of forest types and management treatments in south-east Australia. Undisturbed soil columns were incubated at 20°C for 68 days at near field-capacity water content, and N mineralization was measured in 5-cm depth increments to 30 cm. The soils represented three primary profile forms: gradational, uniform and duplex. They were sampled beneath mature native Eucalyptus sp. forest and from plantations of Pinus radiata of varying age (<1 to 37 years). Several sites had been fertilized, irrigated, or intercropped with lupins. The soils ranged greatly in total soil N concentrations, C:N ratios, total P, and sand, silt, and clay contents. Net N mineralization for individual soil profiles (0–30 cm depth) varied from 2.0 to 66.6 kg ha^-1 over 68 days, with soils from individual depths mineralizing from <0 (immobilization) to 19.3 kg ha^-1 per 5 cm soil depth. Only 0.1–3.1% of the total N present at 0–30 cm in depth was mineralized during the incubation, and both the amount and the percentage of total N mineralized decreased with increasing soil depth. N fertilization, addition of slash residues, or intercropping with lupins in the years prior to sampling increased N mineralization. Several years of irrigation of a sandy soil reduced levels of total N and C, and lowered rates of N mineralization. Considuring all soil depths, the simple linear correlations between soil parameters (C, N, P, C:N, C:P, N:P, coarse sand, fine sand, silt, clay) and N mineralization rates were generally low (r<0.53), but these improved for total N (r=0.82) and organic C (r=0.79) when the soils were grouped into primary profile forms. Prediction of field N-mineralization rates was complicated by the poor correlations between soil properties and N mineralization, and temporal changes in the pools of labile organic-N substrates in the field.     

Effect of pH on nitrogen mineralization in crop-residue-treated soils

Summary This study compares N mineralization in soils treated with crop residues [corn (Zea mays L.), soybean (Glycine max (L.) Merr.), sorghum (Sorghum vulgare Pers.)] or alfalfa (Medicago sativa L.) at three adjusted soil pH values (4, 6, and 8); pH was adjusted with dilute H₂SO₄ or KOH. A sample of soil (20 g) was treated with 0.448 g plant material (equivalent to 50t ha^–1), mixed with 20 g silica sand adjusted to the pH of the soil, and packed in a leaching tube. The soil-sand mixture was leached with 100 ml 5 mM CaCl₂ adjusted to the same pH as that of the treated soil to remove the initial mineral N, and incubated at 30°C. The leaching procedure was repeated every 2 weeks for 20 weeks. Results from three soils showed that N mineralization increased as the soil pH increased. In one soil (Lester soil), significant amounts of NH ₄ ⁺ -N accumulated at pH 4 during the first 12 weeks. Treatment with corn and soybean residues resulted in a marked reduction in N mineralization, especially at pH 4. The percentage of organic N mineralized from sorghum residue and alfalfa added to soils increased as the soil pH increased; the values ranged from 7.7% to 37.0% for sorghum and from 17.2% to 30.1% for alfalfa.     

Soil nitrogen mineralization as affected by water and temperature interactions

Summary The hypothesis that water and temperature interact to influence the rate of soil N mineralization was studied in laboratory incubation experiments with two contrasting soils. Small sample rings (10 mm tall, 50 mm diameter) were packed to uniform bulk density with 1–2 mm aggregates of Plano silt loam and Wacousta silty clay loam. Samples were brought to five different water potentials (–0.1, –0.33, –0.5, –1.0, –3.0 bars) using pressure-plate techniques, and the undisturbed sample rings were then incubated at 10–35°C for 3, 10 or 14 days. The concentration of soil exchangeable NH₄ ⁺-N and NO₃ ^–-N was measured at the end of each incubation period on replicate samples. The Q₁₀ of N mineralization was approximately 2 for all tested water potentials. Soil N mineralization was linearly related to water content or log water potential, but no water-temperature interaction was evident. The Q₁₀ was constant with water content, and the scaled water content-N mineralization relationship was constant with temperature. We recommend the use of scaling approaches for assessing interactive effects between water and other environmental factors on N turnover in soils.     

Tillage and cropping sequence impacts on nitrogen cycling in dryland farming in eastern Montana, USA

Information on N cycling in dryland crops and soils as influenced by long-term tillage and cropping sequence is needed to quantify soil N sequestration, mineralization, and N balance to reduce N fertilization rate and N losses through soil processes. The 21-yr effects of the combinations of tillage and cropping sequences was evaluated on dryland crop grain and biomass (stems + leaves) N, soil surface residue N, soil N fractions, and N balance at the 0–20 cm depth in Dooley sandy loam (fine-loamy, mixed, frigid, Typic Argiboroll) in eastern Montana, USA. Treatments were no-tilled continuous spring wheat (Triticum aestivum L.) (NTCW), spring-tilled continuous spring wheat (STCW), fall- and spring-tilled continuous spring wheat (FSTCW), fall- and spring-tilled spring wheat–barley (Hordeum vulgare L.) (1984–1999) followed by spring wheat–pea (Pisum sativum L.) (2000–2004) (FSTW-B/P), and spring-tilled spring wheat–fallow (STW-F). Nitrogen fractions were soil total N (STN), particulate organic N (PON), microbial biomass N (MBN), potential N mineralization (PNM), NH₄-N, and NO₃-N. Annualized crop grain and biomass N varied with treatments and years and mean grain and biomass N from 1984 to 2004 were 14.3–21.2 kg N ha⁻¹ greater in NTCW, STCW, FSTCW, and FSTW-B/P than in STW-F. Soil surface residue N was 9.1–15.2 kg N ha⁻¹ greater in other treatments than in STW-F in 2004. The STN at 0–20 cm was 0.39–0.96 Mg N ha⁻¹, PON 0.10–0.30 Mg N ha⁻¹, and PNM 4.6–9.4 kg N ha⁻¹ greater in other treatments than in STW-F. At 0–5 cm, STN, PON, and MBN were greater in STCW than in FSTW-B/P and STW-F. At 5–20 cm, STN and PON were greater in NTCW and STCW than in STW-F, PNM and MBN were greater in STCW than in NTCW and STW-F, and NO₃-N was greater in FSTW-B/P than in NTCW and FSTCW. Estimated N loss through leaching, volatilization, or denitrification at 0–20 cm depth increased with increasing tillage frequency or greater with fallow than with continuous cropping and ranged from 9 kg N ha⁻¹ yr⁻¹ in NTCW to 46 kg N ha⁻¹ yr⁻¹ in STW-F. Long-term no-till or spring till with continuous cropping increased dryland crop grain and biomass N, soil surface residue N, N storage, and potential N mineralization, and reduced N loss compared with the conventional system, such as STW-F, at the surface 20 cm layer. Greater tillage frequency, followed by pea inclusion in the last 5 out of 21 yr in FSTW-B/P, however, increased N availability at the subsurface layer in 2004.     

Impacts of elemental S applied under various temperature and moisture regimes on pH and available P in acidic, neutral and alkaline soils

We evaluated the effect of elemental S (S⁰) under three moisture (40, 60, 120% water-filled pore space; WFPS) and three temperature regimes (12, 24, 36°C) on changes in pH and available P (0.5 N NaHCO₃-extractable P) concentrations in acidic (pH 4.9), neutral (pH 7.1) and alkaline (pH 10.2) soils. Repacked soil cores were incubated for 0, 14, 28 and 42 days. Application of S⁰ did not alter the trends of pH in acidic and neutral soils at all moisture regimes but promoted a decrease in the pH of alkaline soil under aerobic conditions (40%, 60% WFPS). Moisture and temperature had profound effects on the available P concentrations in all three soils, accumulation of available P being greatest under flooded conditions (120% WFPS) at 36°C. Application of S⁰ in acidic, neutral and alkaline soils resulted in the net accumulation of 16.5, 14.5 and 13 g P g^–1 soil after 42 days at 60% WFPS, but had no effect under flooded conditions. The greatest available P accumulations in the respective soils were 19, 19.5 and 20 g P g^–1 soil (equivalent to 38, 41, 45 kg P ha^–1) with the combined effects of 36°C, 60% WFPS and applied S⁰. The results of our study revealed that oxidation of S⁰ lowered the pH of alkaline soil (r=–0.88, P<0.01), which in turn enhanced available P concentrations. Also, considering the significant relationship between the release of sulphate and accumulation of P, even in acidic soil (r=0.92, P<0.01) and neutral soil (r=0.85, P<0.01) where the decrease in pH was smaller, it is possible that the stimulatory effect of sulphate on the availability of P was due to its concurrent desorption from the colloidal surface, release from fixation sites and/or mineralization of organic P. Thus, in the humid tropics and irrigated subtropics where high moisture and temperature regimes are prevalent, the application of S⁰ could be beneficial not only in alleviating S deficiency in soils but also for enhancing the availability of P in arable soils, irrespective of their initial pH.     

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.     

Effect of bamboo harvest on dynamics of nutrient pools,N mineralization,and microbial biomass in soil

The effect of harvesting bamboo savanna on the dynamics of soil nutrient pools, N mineralization, and microbial biomass was examined. In the unharvested bamboo site NO _inf3 ^sup- -N in soil ranged from 0.37 to 3.11 mg kg^-1 soil and in the harvested site from 0.43 to 3.67 mg kg^-1. NaHCO₃-extractable inorganic P ranged from 0.55 to 3.58 mg kg^-1 in the unharvested site and from 1.01 to 4.22 mg kg^-1 in the harvested site. Over two annual cycles, the N mineralization range in the unharvested and harvested sites was 0–19.28 and 0–24.0 mg kg^-1 soil month^-1, respectively. The microbial C, N, and P ranges were 278–587, 28–64, and 12–26 mg kg^-1 soil, respectively, with the harvested site exhibiting higher values. Bamboo harvesting depleted soil organic C by 13% and total N by 20%. Harvesting increased N mineralization, resulting in 10 kg ha^-1 additional mineral N in the first 1st year and 5 kg ha^-1 in the 2nd year following the harvest. Microbial biomass C, N and P increased respectively by 10, 18, and 5% as a result of bamboo harvesting.     

Effect of soil characteristics on N mineralization capacity in 112 native and agricultural soils from the northwest of Spain

N mineralization capacity and its main controlling factors were studied in a large variety (n=112) of native (forest, bush) and agricultural (pasture, cultivated) soils from several climatic zones in Spain. The available inorganic N content, net N mineralization, and net N mineralization rate were determined after 6 weeks of aerobic incubation. NH _inf4 ^sup+ –N largely predominated over NO _inf3 ^sup- -N (ratio near 10:1) except in some agricultural soils. Net N mineralization predominated (83% of soils) over net N immobilization, which was more frequent in agricultural soils (25%) than in native soils (9%). In forest soils, both net N mineralization and the net N mineralization rate were significantly higher than in the other soil groups. The net N mineralization rate of pasture and cultivated soils was similar to that of bush soils, but available inorganic N was lower. The net N mineralization rate decreased in the order: soils over acid rocks>soils over sediments>soils over basic rocks or limestone; moreover, the highest net N mineralization and available inorganic N were found in soils over acid rocks. The highest N mineralization was found in soils with low C and N contents, particularly in the native soils, in which N mineralization increased as the C:N ratio increased. N mineralization was higher in soils with a low pH and base saturation than in soils with high pH and base saturation values, which sometimes favoured N immobilization. Soils with an Al gel content of >1% showed lower net N mineralization rates than soils with Al gel contents of <1%, although net N mineralization and available inorganic N did not differ between these groups. The net N mineralization rate in silty soils was significantly lower than in sandy and clayey soils, although soil texture only explained a low proportion of the differences in N mineralization between soils.     

Inhibition of nitrification in soil by heterocyclic nitrogen compounds

Summary The relationship between the structures of diverse heterocyclic nitrogen (N) compounds and the effectiveness of these compounds for the inhibition of nitrification in soil was studied by determining the effects of different amounts of 12 unsubstituted and 33 substituted heterocyclic N compounds on the production of (NO ₂ ^– +NO ₃ ^– )-N in soils incubated at 25 °C for 21 days after treatment with ammonium sulfate. The results showed that unsubstituted heterocyclic N compounds containing two adjacent ring N atoms inhibit nitrification in soil and that two of these compounds, pyrazole and 1,2,4-triazole, are potent inhibitors. They also showed that several substituted pyrazoles and thiadiazoles are good inhibitors of nitrification in soil (e.g., 3-methylpyrazole and 3,4-dichloro-1,2,5-thiadiazole).     

Immobilization of ammonium and nitrate and their interaction with native N in three Illinois Mollisols

Summary Three Illinois Mollisols were incubated for 2 weeks at 25°C after treatment with different amounts of glucose and/or ¹⁵N-labelled (NH₄)₂SO₄ or ¹⁵N-labelled KNO₃. The objectives were: (1) to compare the immobilization and interaction of NH _inf4 ^sup+ –N and NO _inf3 ^sup- –N with the native soil N, and (2) to study the relationship between immobilization of applied N and the added N interaction. As determined, immobilized N refers to forms not extractable with 2 MKCl (immobilized ¹⁵N+clay-fixed ¹⁵NH _inf4 ^sup+ ). In all cases, both NH _inf4 ^sup+ –N and NO _inf3 ^sup- –N were actively immobilized and transformed into organic forms in the presence of glucose. In the absence of glucose, a higher proportion of NH _inf4 ^sup+ than NO _inf3 ^sup- was recovered in organic forms. Although the three soils differed considerably in the amounts of applied N immobilized, similar trends in N immobilization were observed. A positive added N interaction occurred with all soils, the magnitude increasing with the rate of N addition. In the absence of glucose, higher added N interactions were obtained for NH _inf4 ^sup+ than NO _inf3 ^sup- , whereas there was very little difference between NH _inf4 ^sup+ and NO _inf3 ^sup- in the presence of glucose. The results indicate that under conditions of rapid immobilization (e.g., in the presence of glucose), NH _inf4 ^sup+ and NO _inf3 ^sup- will show comparable interaction with the native soil N, whereas in unamended soil, the extent of this interaction will be greater with NH _inf4 ^sup+ than with NO _inf3 ^sup- . Significant correlations were observed between applied N immobilized and the added N interaction only in one soil having a high initial mineral N content.     

Sugar yield,nitrogen uptake by sugar beet and optimal nitrogen fertilization in relation to nitrogen soil analyses and several additional factors

To test the relative usefulness of different methods of chemical analysis for soil nitrogen fractions in the assessment of the fertilizer nitrogen needs of sugar beet, different doses of nitrogen were applied in field experiments laid out during the years 1985–1991. The chemical methods used were N mineral (NO _– ³ +NH ₊ ⁴ ) analyses on soil samples taken in late winter, and extraction with 0.01 M CaCl₂ from soil samples taken the preceding autumn and in late winter. The results of the chemical methods were evaluated in models using estimated optimum nitrogen fertilization, nitrogen present in beets or beets+leaves at leaf maximum and sugar yield as variables. In addition, parameters such as estimates of possible rooting depth and mineralization capacity of the soil were also included in the model. All models for estimating nitrogen fertilization need showed low R ² values. The two methods of soil chemical analysis yielded similar R ² values for nitrogen uptake in plots both with and without nitrogen fertilization. The N mineral method was least useful in predicting sugar yield. Addition of the covariables rooting depth and mineralization capacity appreciably improved the explanatory value of the models with 0.01 M CaCl₂, especially when the analytical results of soil samples taken in autumn were used. For the N mineral method the addition of covariates was found to have far less influence.     

Effects of legume green-manuring on nitrogen mineralization and some microbiological properties in an acid rice soil

We studied N mineralization of legume green manures under laboratory and field conditions, and the effects of field green-manuring on the microbiological properties of an acid Alfisol soil. No significant differences were found in the mineralization rates of Sesbania (Sesbania cannabina), sunnhemp (Crotalaria juncea), and cowpea (Vigna unguiculata) green manure. Mineralization was higher in field-capacity moist soil than water-saturated soil. The decomposition of sunnhemp under field wetland conditions, in the absence of a rice crop, was a rapid as it was under in vitro conditions. The decomposition released considerable amounts of mineral N and the level of NH ₄ ⁺ -N was significantly higher than NO ₃ ^– -N. Significant improvements were observed in the microbial biomass, dehydrogenase activity, and bacterial populations in the field soil green-manured for rice for 3 years, compared with fertilized soil.     

Effect of extracellular-enzyme activities on solubilization rate of soil organic nitrogen

In a sandy soil containing ¹⁵N-labeled active (soluble and easily degradable) and non-labelled passive (recalcitrant) fractions of soil organic matter, the rate of net N mineralization (solubilization) was determined during a 55-day incubation at 25°C, 63% water-holding capacity and different levels of soil extracellular-enzyme activities. The active fraction of soil N was labelled by preincubation (at 5°C and 74% water-holding capacity for 6 months) of soil amended with ¹⁵N-labeled plant material. Increases in the activity of extracellular-enzymes in soil were induced by the addition of glucose and KH₂PO₄ at the beginning of the incubation. The results show that the contents of total soluble N (NO ₃ ^– –N+NH ₄ ⁺ –N + soluble organic N) were significantly higher in glucose-amended soil compared to the unamended soil. The increases in soluble N in soil amended with 1 and 2 mg glucose g^-1 dry soil corresponded to a mean rate of net solubilization of 7.9±1.4 and 18.8±0.7 nmol N g^-1 dry soil day^-1, respectively. The mean rate of net N solubilization (3.6±1.0 nmol N g^-1 dry soil day^-1) in unamended soil was significantly lower than those of glucose amended soils. The content of ¹⁵N in total soluble N in soil amended with 2 mg glucose, for example, was diluted from 3.11±0.08 atom% before the incubation to 2.77±0.03 atom% after 55 days. This indicates that 89% of soluble-N accumulated in soil by the end of the incubation originated from the active fraction of soil N and the rest, estimated at 11%, originated from the passive fraction. The activities of soluble and total proteases as well as the rate of N solubilization in the soil increased with the application of glucose. The activity of these extracellular enzymes was highly correlated with the rates of net N solubilization. Thus, increases in extracellular-enzyme activities in glucose-amended soils had a priming effect on the solubilization of ¹⁵N-labeled active and non-labeled passive fractions of soil organic N. It seems that the activity of extracellular-enzymes expressed in terms of total and soluble protease activities could be a rate-limiting factor in the processes of soil organic N solubilization.     

Nitrogen dynamics in tropical soils of Mali,West Africa

Soil samples were collected from a loamy sand and a clayey soil near Cinzana, Mali, for the purpose of documenting the seasonal dynamics of soil inorganic N after 9 years under five crop-management systems. The cropping systems were: continuous grain sorghum (Sorghum bicolor) or millet (Pennisetum glaucum) without residue return, continuous grain with stalk residue returned to the field every second year, grain in rotation with cowpea (Vigna unguiculata), and grain in rotation with the green manure crops, sesbania (Sesbania rostrata) and dolichos (Dolichos lablab). A sharp increase in soil N was observed early in the rainy season in both soils. Extractable N concentration in loamy sand and clayey soils, respectively, peaked between 15–22 kg and 33–51 kg N ha^–1 in the upper 10 cm of soil. In the clayey soil, the higher soil N concentrations associated with the early season flush lasted 8 weeks after the onset of rain. Nitrogen addition through rotational crops and crop residue was low. Significant improvement of cereal grain yield may not be possible solely by rotation with sesbania and dolichos green manure or cowpea without additional nutrient input. Earlier cereal planting, where feasible, is recommended to improve synchrony of soil N mineralization and crop demand.     

Microbial biomass and mineralization-immobilization of nitrogen in some agricultural soils

Summary The chloroform fumigation-incubation method (CFIM) was used to measure the microbial biomass of 17 agricultural soils from Punjab Pakistan which represented different agricultural soil series. The biomass C was used to calculate biomass N and the changes occurring in NH₄ ⁺-N and NO₃ ^–-N content of soils were studied during the turnover of microbial biomass or added C source. Mineral N released in fumigated-incubated soils and biomass N calculated from biomass C was correlated with some N availability indexes.The soils contained 427–1240 kg C as biomass which represented 1.2%–6.9% of the total organic C in the soils studied. Calculations based on biomass C showed that the soils contained 64–186 kg N ha^–1 as microbial biomass. Immobilization of NCO₃ ^–-N was observed in different soils during the turnover of microbial biomass and any net increase in mineral N content of fumigated incubated soils was attributed entirely to NH₄ ⁺-N.Biomass N calculated from biomass C showed non-significant correlation with different N availability indexes whereas mineral N accumulated in fumigated-incubated soils showed highly significant correlations with other indexes including N uptake by plants.