Estimates of Gross Transformation Rates of Dairy Manure N Using 15N Pool Dilution

Abstract

Most measurements of dairy manure nitrogen (N) availability depend on net changes in soil inorganic N concentration over time, which overlooks the cycling of manure N in the soil. Gross transformations of manure N, including mineralization (m), immobilization (i), and nitrification (n), can be quantified using ¹⁵N pool dilution methods. This research measures gross m, n, and i resulting from application of four freeze‐dried dairy manures that had distinctly different patterns of N availability. A sandy loam soil (coarse‐loamy, mixed, frigid Typic Haplorthod) was amended with four different freeze‐dried dairy manures and incubated at 25°C with optimal soil water content. The dilution of ¹⁵ammonium (NH4⁺) during a 48‐h interval (7–9 d and 56–58 d after manure application) was used to estimate m, whereas the dilution of ¹⁵nitrate (NO₃ ^?) was used to estimate n. Gross immobilization was calculated as gross minus net mineralization. Gross mineralization in the unamended soil was similar at 7‐ to 9‐d and 56‐ to 58‐d intervals and was significantly increased by the application of manures. For both amended and unamended soil, m was much greater (i.e., three‐ to nine‐fold) than estimated net mineralization, illustrating the degree to which manure N can be cycled in soil. At the early interval, both m and i were directly related to the manure C input, demonstrating the linkage between substrate C availability and N utilization by soil microbes. This research clearly shows that the application of dairy manures stimulates gross N transformation rates in the soil, improving our understanding of the impact of manure application on soil N cycling.     

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.     

Microbially-mediated gross N transfer rates in field soils in relation to physico-chemical transfer processes

Abstract

Measurements of gross N transfer in soils have as yet not distinguished between biological or physico-chemical processes. Here, we present a new approach that allows microbially-mediated gross N transfer rates to be estimated in undisturbed soils without adding ¹⁵N. It is based on the assumption that in undisturbed soil, the soil microbial growth rate is equal to its death rate. To assess the contribution of biological versus physico-chemical N transfer processes, we combined the new approach with the ¹⁵N-pool dilution technique. The relationship between both processes varied with soil C and fine particle contents. Nearly equal rates were observed within the carbon-poor soil (0.35% C_org, low fine particle content), whereas up to 2.5 times higher physico-chemical than biological N transfer rates were measured within the carbon-enriched soil (0.86% C_org, higher fine particle content). Furthermore, microbially-mediated gross N transfer rates increased three-fold after N fertilization compared to the unfertilized control.     

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.     

Gross N mineralization rates after application of composted grape marc to soil

Grape marc is a common waste product of the wine production industry. When partially composted and applied to soil it may contain enough N to affect vine growth and hence wine quality. Yet little is known about the quantity and timing of N release from composted grape marc. A laboratory incubation was conducted where composted grape marc amended and non-amended soils were periodically sampled over 148 days at 15 °C for gross N mineralization rates, C mineralization and microbial biomass-C. Gross N mineralization rates were determined by ¹⁵N pool dilution using both analytical equations and the numerical model FLUAZ (Mary, B., Recous, S., Robin, D., 1998. A model for calculating nitrogen fluxes in soil using 15N tracing. Soil Biology & Biochemistry 30, 1963-1979.). Both analytical and FLUAZ determined gross N mineralization rates were in close agreement in the control soil. However, in composted grape marc amended soils there was a discrepancy between the two solutions. Findings indicate that composted grape marc caused a net immobilization of N for the first 50-days of incubation, after which enough N was released to require consideration in fertilizer-N strategies.     

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 decreasing water potential on gross ammonification and nitrification in an acid coniferous forest soil

Changes in the soil water regime, predicted as a consequence of global climate change, might influence the N cycle in temperate forest soils. We investigated the effect of decreasing soil water potentials on gross ammonification and nitrification in different soil horizons of a Norway spruce forest and tested the hypotheses that i) gross rates are more sensitive to desiccation in the Oa and EA horizon as compared to the uppermost Oi/Oe horizon and ii) that gross nitrification is more sensitive than gross ammonification. Soil samples were adjusted by air drying to water potentials from about field capacity to around −1.0 MPa, a range that is often observed under field conditions at our site. Gross rates were measured using the ¹⁵N pool dilution technique. To ensure that the addition of solute label to dry soils and the local rewetting does not affect the results by re-mineralization or preferential consumption of ¹⁵N, we compared different extraction and incubation times.T₀ times ranging from 10 to 300 min and incubation times of 48 h and 72 h did not influence the rates of gross ammonification and nitrification. Even small changes of water potential decreased gross ammonification and nitrification in the O horizon. In the EA horizon, gross nitrification was below detection limit and the response of the generally low rates of gross ammonification to decreasing water potentials was minor. In the Oi/Oe horizon gross ammonification and nitrification decreased from 37.5 to 18.3 mg N kg⁻¹ soil d⁻¹ and from 15.4 to 5.6 mg N kg⁻¹ soil d⁻¹ when the water potential decreased from field capacity to −0.8 MPa. In the Oa horizon gross ammonification decreased from 7.4 to 4.0 mg N kg⁻¹ soil d⁻¹ when the water potential reached −0.6 MPa. At such water potential nitrification almost ceased, while in the Oi/Oe horizon nitrification continued at a rather high level. Hence, only in the Oa horizon nitrification was more sensitive to desiccation than ammonification. Extended drought periods that might result from climate change will cause a reduction in gross N turnover rates in forest soils even at moderate levels of soil desiccation.     

Immobilization and remineralization of N following addition of wheat straw into soil: determination of gross N transformation rates by N-ammonium isotope dilution technique

N dynamics in soil where wheat straw was incorporated were investigated by a soil incubation experiment using ¹⁵N-labelled nitrate or ¹⁵N-labelled wheat straw. The incubated soils were sampled after 7, 28, 54 days from the incorporation of wheat straw, respectively, and gross rates of N transformations including N remineralization and temporal changes in the amount of microbial biomass were determined.Following the addition of wheat straw into soils, rapid decrease of nitrate content in soil and increase of microbial biomass C and N occurred within the first week from onset of the experiment. Both the gross rates of mineralization and immobilization determined by ¹⁵N-ammonium isotope dilution technique were remarkably enhanced by the addition of wheat straw, and gradually decreased with time. Remineralization rate of N derived from ¹⁵N-labelled nitrate, and mineralization rate of N derived from ¹⁵N-labelled wheat straw was estimated by ¹⁵N isotope dilution technique using non-labelled ammonium. Remineralization rates of N derived from ¹⁵N-labelled nitrate were calculated to be 0.71 mg N kg⁻¹ d⁻¹ after 7 days, 0.55 mg N kg⁻¹ d⁻¹ after 28 days, and 0.29 mg N kg⁻¹ d⁻¹ after 54 days.Nearly 10% of the ¹⁵N-labelled N originally contained in the wheat straw was held in the microbial biomass irrespective of the sampling time. The amount of inorganic N in soil which was derived from ¹⁵N-labelled wheat straw ranged between 1.93 and 2.37 mg N kg⁻¹.Rates of N transformations in soil with ¹⁵N-labelled wheat straw were obtained by assuming that the k value was equal to the ¹⁵N abundance of biomass N, and the obtained values were considered to be valid.     

Long‐term field fertilization affects soil nitrogen transformations in a rice‐wheat‐rotation cropping system

Mineralization and nitrification are the key processes of the global N cycle and are primarily driven by microorganisms. However, it remains largely unknown about the consequence of intensified agricultural activity on microbial N transformation in agricultural soils. In this study, the ¹⁵N‐dilution technique was carried out to investigate the gross mineralization and nitrification in soils from a long‐term field fertilization experiment starting from 1988. Phospholipid fatty acids (PLFA) analysis was used to determine soil microbial communities, e.g., biomasses of anaerobic bacterial, bacterial, fungi, and actinobacteria. The abundance of ammonia‐oxidizing bacteria (AOB) and archaea (AOA) were measured using real‐time quantitative polymerase chain reaction. The results have demonstrated significant stimulation of gross mineralization in the chemical‐fertilizers treatment (NPK) ([6.53 ± 1.29] mg N kg^–1 d^–1) and chemical fertilizers–plus–straw treatment (NPK+S1) soils ([8.13 ± 1.68] mg N kg^–1 d^–1) but not in chemical fertilizers–plus–two times straw treatment (NPK+S2) soil when compared to the control‐treatment (CK) soil ([3.62 ± 0.86] mg N kg^–1 d^–1). The increase of anaerobic bacterial biomass is up to 6‐fold in the NPK+S2 compared to that in the CK soil ([0.7 ± 0.5] nmol g^–1), implying that exceptionally high abundance of anaerobic bacteria may inhibit gross mineralization to some extent. The gross nitrification shows upward trends in the NPK+S1 and NPK+S2 soils. However, it is only significantly higher in the NPK soil ([5.56 ± 0.51] mg N kg^–1 d^–1) compared to that in the CK soil ([3.70 ± 0.47] mg N kg^–1 d^–1) (p < 0.05). The AOB abundance increased from (0.28 ± 0.07) × 10⁶ copies (g soil)^–1 for the CK treatment to (4.79 ± 1.23) × 10⁶ copies (g soil)^–1 for the NPK treatment after the 22‐year fertilization. In contrast, the AOA abundance was not significantly different among all treatment soils. The changes of AOB were well paralleled by gross nitrification activity (gross nitrification rate = 0.263 AOB + 0.047 NH ‐N + 2.434, R² = 0.73, p < 0.05), suggesting the predominance of bacterial ammonia oxidation in the fertilized fields.     

Liming effects on some chemical and biological parameters of soil (spodosols and histosols) in a hardwood forest watershed

Acidic lakes and streams can be restored with base application (usually limestone) provided that the base does not wash out before the benefits of alkalization can be realized; liming soils of the adjoining watershed may be an alternative approach. This study was conducted to provide a scientific basis for soil liming. Plots (50 m²) with different limestone dosages (e.g. 0, 5, 10 or 15 Mg CaCO₃ ha^?1) were established on each of two different soils (a Spodosol and a Histosol) in the Woods Lake watershed of the Adirondack Park Region of New York, USA. Six months after soil liming much of the added limestone was still present in both the Spodosol and in the Histosol. Ten months after soil liming results indicated that: (1) soil pH increased (>1 unit) but mostly in the top 1 cm; (2) net N mineralization increased from 9.6 to ca. 15 µg N g^?1 d^?1 and nitrification increased from 2.8 to ca. 8 µg N g^?1 d^?1; (3) denitrification was not affected (98 µg N g^?1 d^?1); (4) CO₂ production potential decreased in the surface soil and as a function of limestone dosage (60 to 6 µmol g^?1 d^?1); and (5) soluble SO ₄ ^2? concentrations in the Histosol were not affected (105 µmol L^?1). Liming acidic forest soils with >5 Mg CaCO₃ ha^?1 may increase the soil's acid neutralizing capacity, which could provide long-term benefits for surface water acidification.     

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.     

Gross nitrogen transformations in adjacent native and plantation forests of subtropical Australia

The impact of land-use change on soil nitrogen (N) transformations was investigated in adjacent native forest (NF), 53 y-old first rotation (1R) and 5 y-old second rotation (2R) hoop pine (Araucaia cunninghamii) plantations. The ¹⁵N isotope dilution method was used to quantify gross rates of N transformations in aerobic and anaerobic laboratory incubations. Results showed that the land-use change had a significant impact on the soil N transformations. Gross ammonification rates in the aerobic incubation ranged between 0.62 and 1.78 mg N kg⁻¹ d⁻¹, while gross nitrification rates ranged between 2.1 and 6.6 mg N kg⁻¹ d⁻¹. Gross ammonification rates were significantly lower in the NF and the 1R soils than in the 2R soils, however gross nitrification rates were significantly higher in the NF soils than in the plantation soils. The greater rates of gross nitrification found in the NF soil compared to the plantation soils, were related to lower soil C:N ratios (i.e. more labile soil N under NF). Nitrification was found to be the dominant soil N transformation process in the contrasting forest ecosystems. This might be attributed to certain site conditions which may favour the nitrifying community, such as the dry climate and tree species. There was some evidence to suggest that heterotrophic nitrifiers may undertake a significant portion of nitrification.     

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.     

Heterotrophic and autotrophic nitrification in two acid pasture soils

Laboratory incubation experiments, using ¹⁵N-labeling techniques and simple analytical models, were conducted to measure heterotrophic and autotrophic nitrification rates in two acid soils (pH 4.8-5.3; 1/5 in H₂O) with high organic carbon contents (6.2-6.8% in top 5 cm soil). The soils were from pastures located near Maindample and Ruffy in the Northeast Victoria, Australia. Gross rates of N mineralization, nitrification and immobilization were measured. The gross rates of autotrophic nitrification were 0.157 and 0.119 μg N g⁻¹ h⁻¹ and heterotrophic nitrification rates were 0.036 and 0.009 μg N g⁻¹ h⁻¹ for the Maindample and Ruffy soils, respectively. Heterotrophic nitrification accounted for 19% and 7% of the total nitrification in the Maindample and Ruffy soils, respectively. The heterotrophic nitrifiers used organic N compounds and no as the substrate for nitrification.     

Cold storage and laboratory incubation of intact soil cores do not reflect in-situ nitrogen cycling rates of tropical forest soils

Measurements of N transformation rates in tropical forest soils are commonly conducted in the laboratory from disturbed or intact soil cores. On four sites with Andisol soils under old-growth forests of Panama and Ecuador, we compared N transformation rates measured from laboratory incubation (at soil temperatures of the sites) of intact soil cores after a period of cold storage (at 5 °C) with measurements conducted in situ. Laboratory measurements from stored soil cores showed lower gross N mineralization and NH₄⁺ consumption rates and higher gross nitrification and NO₃⁻ immobilization rates than the in-situ measurements. We conclude that cold storage and laboratory incubation change the soils to such an extent that N cycling rates do not reflect field conditions. The only reliable way to measure N transformation rates of tropical forest soils is in-situ incubation and mineral N extraction in the field.     

Fate of residual 15N-labeled fertilizer in dryland farming systems on soils of contrasting fertility

Abstract

Up to 50% of nitrogen (N) fertilizer can remain in soil after crop harvest in dryland farming. Understanding the fate of this residual fertilizer N in soil is important for evaluating its overall use efficiency and environmental effect. Nitrogen-15 (¹⁵N)-labeled urea (165 kg N ha^?1) was applied to winter wheat (Triticum aestivum L.) growing in three different fertilized soils (no fertilizer, No-F; inorganic nitrogen, phosphorus and potassium fertilization, NPK; and manure plus inorganic NPK fertilization, MNPK) from a long-term trial (19 years) on the south of the Loess Plateau, China. The fate of residual fertilizer N in soils over summer fallow and the second winter wheat growing season was examined. The amount of the residual fertilizer N was highest in the No-F soil (116 kg ha^?1), and next was NPK soil (60 kg ha^?1), then the MNPK soil (43 kg ha^?1) after the first winter wheat harvest. The residual fertilizer N in the No-F soil was mainly in mineral form (43% of the residual ¹⁵N), and for the NPK and MNPK soils, it was mainly in organic form. The loss rate of residual ¹⁵N in No-F soil over summer fallow was as high as 48%, and significantly (P < 0.05) higher than that in the NPK soil (22%) and MNPK soil (19%). The residual ¹⁵N use efficiency (RNUE) by the second winter wheat was 13% in the No-F soil, 6% in the NPK soil and 8% in the MNPK soil. These were equivalent to 9.0, 2.0 and 2.2% of applied ¹⁵N. The total ¹⁵N recovery (¹⁵N uptake by crops and residual in 0–100 cm soil layer) in the MNPK and NPK soils (84.5% and 86.6%, respectively) were both significantly higher than that in the No-F soil (59%) after two growing seasons. The ¹⁵N uptake by wheat in two growing seasons was higher in the MNPK soil than in NPK soil. Therefore, we conclude that a high proportion of the residual ¹⁵N was lost during the summer fallow under different land management in dryland farming, and that long-term combined application of manure with inorganic fertilizer could increase the fertilizer N uptake and decrease N loss.     

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.     

Arginine ammonification assay as a rapid index of gross N mineralization in agricultural soils

Seasonal dynamics of in situ gross nitrogen (N) mineralization rates were measured using the ¹⁵N-NH₄⁺ isotope dilution method in a Danish soil subjected to four different agricultural practices (set aside, barley, winter wheat and clover). Results were compared to arginine ammonification in the soil samples measured as NH₄⁺ production following addition of excess (1 mM) arginine. In the set aside, barley, winter wheat and clover soils the average annual rates of gross N mineralization (0.29, 0.60, 1.34 and 1.75 µg NH₄⁺-N g^-1 day^-1, respectively) and arginine ammonification activity (0.21, 0.55, 0.88, and 1.33 µg NH₄⁺-N g^-1 h^-1, respectively) were well correlated. Furthermore, the seasonal variations of gross N mineralization and arginine ammonification activities were very similar, showing rapid responses to rainfall and generally higher activities in wetted soils. As tested in the laboratory, the arginine ammonification activity correlated well with heterotrophic microbial respiration activity (CO₂ production) in soil samples and further displayed a simple, one-component Michaelis-Menten kinetics with a high affinity for arginine (K_m value of 48 µM LJ µM) as determined from non-linear parameter estimation. This indicated that arginine ammonification activity was primarily due to microorganisms, and the activity was also shown to be at a minimum in sterile soil samples. All evidence thus supported that our standard assay of arginine ammonification activity provides a good index of gross N mineralization rates by the microorganisms in soil under in situ conditions.     

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.