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.     

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.     

Carbon mineralization kinetics as influenced by soil properties

In a short-term laboratory study C mineralization potentials were determined on soil samples obtained from some representative agricultural soils in Tuscany, Italy. All the kinetic models tested to describe the mineralization process provided a good fit to the experimental data. A modified first-order model best described C mineralization in the soil. Both potentially mineralizable C and the mineralization rate (k) varied considerably among soils, reflecting the differences in soil properties. Potentially mineralizable C was positively related to C evolved as CO₂ and to the exchange capacity. Normalized values (potentially mineralizable C divided by organic C), representing on average about 2% of the total soil C, was positively correlated to soil pH and negatively to the soil C pool, the soil N pool, and total microbial activity. Values for k ranged between 0.050 and 0.104 day^-1, being higher in fine-textured soils and in soils with a large free Fe content. A low C:N ratio was indicative of a high k value. Turnover times for mineralized C were relatively rapid, ranging from 10 to 20 days.     

Mineralization of carbon and nitrogen from fresh and anaerobically stored sheep manure in soils of different texture

A sandy loam soil was mixed with three different amounts of quartz sand and incubated with (¹⁵NH₄)₂SO₄ (60 g N g^-1 soil) and fresh or anaerobically stored sheep manure (60 g g^-1 soil). The mineralization-immobilization of N and the mineralization of C were studied during 84 days of incubation at 20°C. After 7 days, the amount of unlabelled inorganic N in the manure-treated soils was 6–10 g N g^-1 soil higher than in soils amended with only (¹⁵NH₄)₂SO₄. However, due to immobilization of labelled inorganic N, the resulting net mineralization of N from manure was insignificant or slightly negative in the three soil-sand mixtures (100% soil+0% quartz sand; 50% soil+50% quartz sand; 25% soil+75% quartz sand). After 84 days, the cumulative CO₂ evolution and the net mineralization of N from the fresh manure were highest in the soil-sand mixutre with the lowest clay content (4% clay); 28% fo the manure C and 18% of the manure N were net mineralized. There was no significant difference between the soil-sand mixtures containing 8% and 16% clay, in which 24% of the manure C and -1% to 4% of the manure N were net mineralized. The higher net mineralization of N in the soil-sand mixture with the lowest clay content was probably caused by a higher remineralization of immobilized N in this soil-sand mixture. Anaerobic storage of the manure reduced the CO₂ evolution rates from the manure C in the three soil-sand mixtures during the initial weeks of decomposition. However, there was no effect of storage on net mineralization of N at the end of the incubation period. Hence, there was no apparent relationship between net mineralization of manure N and C.     

Nitrogen transformations in cold and frozen agricultural soils following organic amendments

Though microbial activity is known to occur in frozen soils, little is known about the fate of animal manure N applied in the fall to agricultural soils located in areas with prolonged winter periods. Our objective was to examine transformations of soil and pig slurry N at low temperatures. Loamy and clay soils were either unamended (Control), amended with ¹⁵NH₄-labeled pig slurry, or amended with the pig slurry and wheat straw. Soils were incubated at −6, −2, 2, 6, and 10 °C. The amounts of NH₄, NO₃ and microbial biomass N (MBN), and the presence of ¹⁵N in these pools were monitored. Total mineral N, NO₃ and ¹⁵NO₃ increased at temperature down to −2 °C in the loam soil and −6 °C in the clay soil, indicating that nitrification and mineralization proceeded in frozen soils. Nitrification and mineralization rates were 1.8-4.9 times higher in the clay than in the loamy soil, especially below freezing point (3.2-4.9), possibly because more unfrozen water remained in the clay than in the loamy soil. Slurry addition increased nitrification rates by 3-14 times at all temperatures, indicating that this process was N-limited even in frozen soils. Straw incorporation caused significant net N immobilization only at temperatures ≥2 °C in both soils; the rates were 1.4-3.4 higher in the loam than in the clay soil. Nevertheless, up to 30% of the applied ¹⁵N was present in MBN at all temperatures. These findings indicate that microbial N immobilization occurred in frozen soils, but was not strong enough to induce net immobilization below the freezing point, even in the presence of straw. The Q₁₀ values for estimated mineralization and nitrification rates were one to two orders-of-magnitude larger below 2 °C than above this temperature (13-208 versus 1.5-6.9, respectively), indicating that these processes are highly sensitive to a small increase in soil temperature around the freezing point of water. This study confirms that net mineralization and nitrification can occur at potentially significant rates in frozen agricultural soils, especially in the presence of organic amendments. In contrast, net N immobilization could be detected essentially above the freezing point. Our results imply that fall-applied N could be at risk of overwinter losses, particularly in fine-textured soils.     

Effect of organic residue amendment on mineralization of nitrogen in flooded rice soils under laboratory conditions

Abstract

This study was undertaken to assess the mineralization of nitrogen (N) in rice soils amended with organic residues under flooded condition. A lab incubation study with a 3x3 factorial design (two replications) was conducted with three rice soils (Joydebpur, Faridpur, and Thakurgaon) receiving the following treatments: 1) control, 2) rice straw (Oryza sativa L.), or 3) pea vine (Pisum sativum L.). The organic residue (25 mg straw g^‐1 soil) was mixed with soil and glass beads (1:1, soil to beads ratio), and transferred into a Pyrex leaching tube, flooded and then incubated at 35°C for up to 12 weeks. The soils in the leaching tubes were leached (while maintaining flooded condition) at 1,2,4, 8, and 12 weeks with deionized water for determination of NH₄‐N, NO₃‐N, pH, and Eh. Nitrogen mineralization in soils amended with rice straw was somewhat different than that of soils treated with pea vine. Soil treated with rice straw had a higher N mineralization rate than soils treated with pea vine, which was due to a lower carbon (C):N ratio for rice straw. The potentially mineralizable N pool (N_o) in soils amended with rice straw and pea vine under flooded conditions, estimated using a 1st order exponential equation, were 7 to 15 times, and 3 to 9 times greater for rice straw N_o values and pea vine, respectively, than the control. The K_N values for unamended soils ranged from 0.35 to 0.52 mg N kg^‐1 wk^‐1 and rice straw and pea vine treated soils were from 0.75 to 1.22 and 0.46 to 0.58 mgN kg^‐1 wk^‐1. The lower N_o and K_N values in pea vine treatments suggested there was greater immobilization of N than in rice straw treatments.     

Relationships between carbon dioxide emission and soil properties in salt-affected landscapes

Net carbon dioxide (CO₂) emission from soils is controlled by the input rate of organic material and the rate of decomposition which in turn are affected by temperature, moisture and soil factors. While the relationships between CO₂ emission and soil factors are well-studied in non-salt-affected soils, little is known about soil properties controlling CO₂ emission from salt-affected soils. To close this knowledge gap, non-salt-affected and salt-affected soils (0-0.30 m) were collected from two agricultural regions: in India (irrigation induced salinity) and in Australia (salinity associated with ground water or non-ground water associated salinity). A subset (50 Indian and 70 Australian soils) covering the range of electrical conductivity (EC) and sodium adsorption ratio (SAR) in each region was used in a laboratory incubation experiment. The soils were left unamended or amended with mature wheat residues (2% w/w) and CO₂ release was measured over 120 days at constant temperature and soil water content. Residues were added to overcome carbon limitation for soil respiration. For the unamended soils, separation in multidimensional scaling plots was a function of differences in soil texture (clay, sand), SOC pools (particulate organic carbon (POC) and humus-C) and also EC. Cumulative CO₂-C emission from unamended and amended soils was related to soil properties by stepwise regression models. Cumulative CO₂-C emission was negatively correlated with EC in saline soils (R² = 0.50, p < 0.05) from both regions. In the unamended non-salt-affected soils, cumulative CO₂-C emission was significantly positively related to the content of POC for the Indian soils and negatively related to clay content for the Australian soils. In the wheat residue amended soils, cumulative CO₂-C emission had positive relationship with POC and humus-C but a negative correlation with EC for both Indian and Australian soils. SAR was negatively related (β = −0.66, p < 0.05) with cumulative CO₂-C emission only for the unamended saline-sodic soils of Australia. Cumulative CO₂-C emission was significantly negatively correlated with bulk density in amended soils from both regions. The study showed that in salt-affected soils, EC was the main factor influencing for soil respiration but the content of POC, humus-C and clay were also influential with the magnitude of influence depending on whether the soils were salt affected or not.     

Long-Term Cultivation Effects on Biological C and N Fractions in a Fluvaquentic Haplustolls of Semi-arid Region of the Northern Turkey

Conversion of a native ecosystem can impact the nature and dynamics of organic carbon (C) fractions. The goal of this study was to determine the effects of cultivation and monoculture wheat production on soil organic C and biological C fractions compared to a previously flooded native pasture in northern Turkey. Soil samples were collected from four randomly selected locations of each management system. Some soil chemical [pH, calcium carbonate (CaCO₃), total nitrogen (N), and organic C], physical (sand, clay, and silt), and biological properties [microbial biomass carbon (MBC), mineralizable C, and mineralizable N] were measured. Conversion of pasture to cultivated land slightly increased soil pH, but CaCO₃, total organic C (TOC), and N contents were significantly (P < 0.05) decreased with cultivation. Total organic C and N contents were more than three times less in cultivated soils compared to pasture. Microbial biomass C was significantly decreased (P < 0.05) with long-term cultivation, and the greater seasonal fluctuations were measured at the surface of both ecosystems. The greatest level of potentially mineralizable C was observed in the pasture rather than the cultivated soil, but the proportional distribution of mineralized C to TOC was greater in the cultivated soil. These results suggested that the long-term cultivation (15 years) of previously flooded native ecosystems increased C mineralization and resulted in 72% C loss at the surface soil. Cultivated soils have a greater potential to restore atmospheric carbon dioxide (CO₂) if proper cultivation and management systems are used.     

Impact of addition of different rates of rice-residue biochar on C and N dynamics in texturally diverse soils

Impacts of crop residue biochar on soil C and N dynamics have been found to be subtly inconsistent in diverse soils. In the present study, three soils differing in texture (loamy sand, sandy clay loam and clay) were amended with different rates (0%, 0.5%, 1%, 2% and 4%) of rice-residue biochar and incubated at 25°C for 60 days. Soil respiration was measured throughout the incubation period whereas, microbial biomass C (MBC), dissolved organic C (DOC), NH₄⁺-N and NO₃^–N were analysed after 2, 7, 14, 28 and 60 days of incubation. Carbon mineralization differed significantly between the soils with loamy sand evolving the greatest CO₂ followed by sandy clay loam and clay. Likewise, irrespective of the sampling period, MBC, DOC, NH₄⁺-N and NO₃^–N increased significantly with increasing rate of biochar addition, with consistently higher values in loamy sand than the other two soils. Furthermore, regardless of the biochar rates, NO₃^–-N concentration increased significantly with increasing period of incubation, but in contrast, NH₄⁺-N temporarily increased and thereafter, decreased until day 60 in all soils. It is concluded that C and N mineralization in the biochar amended soils varied with the texture and native organic C status of the soils.     

添加表面活性剂土壤中蒽的去除以及矿质态氮动态研究

Surfactants, such as non-ionic Surfynol 485 （ethoxylated 2,4,7,9-tetramethyl-5-decyne-4,7-diol）, have been applied to accelerate removal of polycyclic aromatic hydrocarbons from soil. This study investigated the dissipation of anthracene, and carbon （C） and nitrogen （N） mineralization in soil amended with non-ionic Surfynol 485 at different rates. Soil samples of a Typic Fragiudept taken from Otumba, Mexico were spiked with anthracene at a final concentration of 520 mg kg^-1 dry soil using acetone as solvent, amended with 0.0, 24.9, 49.8 or 124.4 g kg^-1 soil of the surfactant and incubated in the laboratory. The soil not amended with anthracene, acetone and the surfactant was used as a control. Dynamics of C and N and the concentration of anthracene were monitored for 56 d. After 56 d of incubation, 38% of the anthracene was removed from the unamended soil, and 47%, 55% and 66% of the anthracene were removed when 24.9, 49.8 and 124.4 g kg^-1 of the surfactant were applied, respectively. Application of acetone, anthracene or surfactant increased the emission of CO2, but decreased the mineral N compared to the unamended control. Applying the surfactant to the acetone or anthracene-amended soil reduced emission of CO2, but increased the mineral N at the lower application rates of the surfactant. It was found that the application of the non-ionic surfactant increased the bioavailability of anthracene and thus its removal from soil, increased C mineralization, but decreased N miaeralization. Consequently, the application of non-ionic surfactant could be easily used to accelerate the removal of pollutants from hydrocarbon-contaminated soils, but mineral N in the soil would decrease, which might inhibit plant growth.     

Studies of nitrogen immobilization and mineralization in calcareous soils—II: Mineralization of immobilized nitrogen from soil fractions of different particle size and density

¹⁵NO^?₃ was immobilized in a calcareous sandy soil and a calcareous clay soil each incubated with glucose and wheat straw. Net mineralization of organic-¹⁵N was more rapid in the sandy soil, irrespective of C amendment, and in soils amended with glucose. Intermittent drying and wetting of soils during incubation stimulated mineralization of ¹⁵N-labelled and native soil organic-N in all treatments. The availability (percentage mineralization) of recently-immobilized ¹⁵N consistently exceeded that of the native soil N. Ratios of the availability of labelled and unlabelled N were similar in the sandy and clay soils but varied according to C amendment, drying and wetting cycle and incubation period.Changes in the distribution of immobilized N amongst soil extracts and soil fractions of different particle size and density were determined during periods of net N mineralization. In straw-amended soils, the organic-¹⁵N of a light fraction, sp.gr. < 1.59, decomposed relatively rapidly during the late mineralization period. Decreases of organic ¹⁵N of the fine clay fraction were also recorded. In glucose-amended soils, net N mineralization was accompanied by significant decreases in the concentrations of organic-¹⁵N of the silt and fine clay fractions.Drying and rewetting of soils hastened or magnified changes occurring in the organic-¹⁵N of soil fractions, but qualitatively, the pattern of change was similar to that observed with soils incubated under uniformly-moist conditions.The percentage distribution of labelled and unlabelled N suggested that in the long term, the silt fraction will accumulate an increasing proportion of the more stable nitrogenous residues.     

Carbon mineralization in soils of different textures as affected by water-soluble organic carbon extracted from composted dairy manure

The water-soluble organic C in composted manure contains a portion of labile C which can stimulate soil microbial activity. The objective of this experiment was to evaluate the effects of water-soluble organic C extracted from composted dairy manure on C mineralization in soil with different textures. Three soils with textures varying from 3 to 54% clay were amended with 0 to 80 mg water-soluble organic C kg^–1 soil extracted from a composted dairy manure and incubated for 16 weeks at 23°C. The total amount of C mineralized was greater than the amount of C added in the three soils. Differences in mineralizable C with and without added water-soluble organic C were approximately 13–16 times, 4.8–8 times, and 7.5–8 times greater than the amount of C added to clay, loam, and sand soils, respectively. The results of this experiment suggest that immediately following composted manure applications, C mineralization rates increase, and that most of the C mineralized comes mainly from the indigenous soil organic C pool.CLBRR contribution No. 94-71     

Pedotransfer functions for the pool size of slowly mineralizable organic N in sandy arable soils

The major aim of this study was to evaluate how the pool size of slowly mineralizable, ‘old’ soil organic N can be derived from more easily accessible soil and site information via pedotransfer functions (PTF). Besides modeling, this pool size might be of great importance for the identification of soils with high mineralization potential in drinking‐water catchments. From long‐term laboratory incubations (ca. 200 days) at 35 °C, the pool sizes of easily mineralizable organic N (N_fast), mainly in fresh residues, and slowly mineralizable, ‘old’ soil organic N (N_slow) as well as their first‐order rate coefficients were obtained. 90 sandy arable soils from NW Germany served to derive PTFs for N_slow that were evaluated using another 20 soils from the same region. Information on former land‐use and soil type was obtained from topographical, historical, and soil maps (partly from 1780). Pool size N_slow very strongly depends on soil type and former land‐use. Mean pool sizes of N_slow were much lower in old arable lowland (105 mg N kg^–1) than upland soils (175 mg N kg^–1) possibly due to lower clay contents. Within lowlands, mean pool sizes in former grassland soils (245 mg N kg^–1) were 2 to 3 times larger than in old arable soils due to accumulation of mineralizable N. In contrast, mean pool sizes of N_slow were lowest in recently cleared, former heath‐ and woodland (31 mg N kg^–1) as a result of the input of hardly decomposable organic matter. Neither N nor C in the light fraction (density < 1.8 g cm^–3) was adequate to derive pool size N_slow in the studied soils (r² < 0.03). Instead, N_slow can be accurately (r² = 0.55 – 0.83) derived from one or two basic soil characteristics (e.g. organic C, total N, C : N, mineral fraction < 20 μm), provided that sites were grouped by former land‐use. Field mineralization from N_slow during winter (independent data set) can be predicted as well on the basis of N_slow‐values calculated from PTFs that were derived after grouping the soils by former land‐use (r² = 0.51***). In contrast, using the PTF without soil grouping strongly reduced the reliability (r² = 0.16).     

Boiling Potassium Chloride–Extractable Nitrogen as an Index of Potentially Mineralizable and Plant‐Available Nitrogen in Soil

Abstract

Mineralization of soil organic nitrogen (N) and its contribution toward crop N uptake is central to developing efficient N‐management practices. Because biological incubation methods are time consuming and do not fit into the batch‐analysis techniques of soil‐testing laboratories, an analytical procedure that can provide an estimate of the mineralizable N would be useful as a soil‐test method for predicting plant‐available N in soil. In the present studies, the ability of boiling potassium chloride (KCl) to extract potentially mineralizable and plant‐available N in arable soils of semi‐arid India was tested against results from biological incubations and uptake of N by wheat in a pot experiment. Mineralization of organic N in soils was studied in the laboratory by conducting aerobic incubations for 112 days at 32°C and 33 KPa of moisture. Cumulative N mineralization in different soils ranged from 8.2 to 75.6 mg N kg^?1 soil that constituted 2.7 to 8.8% of organic N. The amount of mineral N extracted by KCl increased with increase in length of boiling from 0.5 to 2 h. Boiling for 0.5, 1, 1.5, and 2 h resulted in an increase in mineral‐N extraction by 9.3, 12.7, 19.6, and 26.1%, respectively, as compared to mineral N extracted at room temperature. The boiling‐KCl‐hydrolyzable N (ΔN_i) was directly dependent upon soil organic N content, but the presence of clay retarded hydrolysis for boiling lengths of 0.5 and 1 h. However, for boiling lengths of 1.5, and 2 h, the negative effect of clay was not apparent. The ΔN _i was significantly (P=0.05) correlated to cumulative N mineralized and N‐mineralization potential (N₀). The relationship between N₀ and ΔN _i was curvilinear and was best described by a power function. Boiling length of 2 h accounted for 78% of the variability in N₀. Results of the pot experiment showed that at 21‐ and 63‐day growth stages, dry‐matter yield and N uptake by wheat were significantly correlated to boiling‐KCl‐extractable mineral N. Thus, boiling KCl could be used to predict potentially mineralizable and plant‐available N in these soils, and a boiling time of 2 h was most suitable to avoid the negatively affected estimates of boiling‐KCl‐hydrolyzable N in the presence of clay. The results have implications for selecting length of boiling in soils varying widely in clay content, and this may explain why, in earlier studies, longer boiling times (viz. 2 or 4 h) were better predictors of N availability as compared to 0.5 and 1 h.     

Short-term carbon mineralization in saline–sodic soils

Previous studies have shown that carbon (C) mineralization in saline or sodic soils is affected by various factors including organic C content, salt concentration and water content in saline soils and soil structure in sodic soils, but there is little information about which soil properties control carbon dioxide (CO₂) emission from saline-sodic soils. In this study, eight field-collected saline–sodic soils, varying in electrical conductivity (EC_e, a measure of salinity, ranging from 3 to 262 dS m⁻¹) and sodium adsorption ratio (SAR_e, a measure of sodicity, ranging from 11 to 62), were left unamended or amended with mature wheat or vetch residues (2% w/w). Carbon dioxide release was measured over 42 days at constant temperature and soil water content. Cumulative respiration expressed per gram SOC increased in the following order: unamended soil<soil amended with wheat residues (C/N ratio 122)<soil with vetch residue (C/N ratio 18). Cumulative respiration was significantly (p < 0.05) negatively correlated with EC_e but not with SAR_e. Our results show that the response to EC_e and SAR_e of the microbial community activated by addition of organic C does not differ from that of the less active microbial community in unamended soils and that salinity is the main influential factor for C mineralization in saline–sodic soils.     

Extractability of labelled microbial biomass N by electro-ultrafiltration and CaCl2 extraction

A laboratory soil incubation and a pot experiment with ryegrass were carried out in order to examine the extractability of microbial biomass N by using either 10-mM CaCl₂ extraction or the electro-ultrafiltration (EUF) method. The aim of the experiment was to test the hypothesis whether the organic N (Norg) extracted by EUF or CaCl₂ from dried soil samples represents a part of the microbial biomass. For the laboratory incubation a ¹⁵N-labelled Escherichia coli suspension was mixed with the soil. For the pot experiment a suspension of ¹⁵N-labelled bacteria was applied which had previously been isolated from the soil used. Soil samples of both treatments, with and without applied bacterial suspension, were extracted by EUF and CaCl₂. The extractability of applied microbial biomass was estimated from the difference in extractable Norg between the two treatments. In addition, the N isotopic composition in the upper plant matter, in the soil, and in organic and inorganic N fractions of EUF and CaCl₂ extracts was analysed. Both experiments showed that the applied microbial biomass was highly accessible to mineralization and thus represented potentially mineralizable N. However, this mineralizable N was not extractable by CaCl₂ or by the EUF method. It was, therefore, concluded that the organic N released on soil drying and which was thus extractable was derived from the non-biomass soil organic matter. The result suggests that both extraction methods may provide a suitable index for mineralizable N only in cases where the decomposable organic substrates are derived mainly from sources other than the living soil biota.Dedicated to Professor J. C. G. Ottow on the occasion of his 60th birthday     

Carbon mineralization in subtropical alluvial arable soils amended with sugarcane bagasse and rice husk biochars

Subtropical recent alluvial soils are low in organic carbon (C). Thus, increasing organic C is a major challenge to sustain soil fertility. Biochar amendment could be an option as biochar is a C-rich pyrolyzed material, which is slowly decomposed in soil. We investigated C mineralization (CO₂-C evolution) in two types of soils (recent and old alluvial soils) amended with two feedstocks (sugarcane bagasse and rice husk) (1%, weight/weight), as well as their biochars and aged biochars under a controlled environment (25 ±2 ℃) over 85 d. For the recent alluvial soil (charland soil), the highest absolute cumulative CO₂-C evolution was observed in the sugarcane bagasse treatment (1 140 mg CO₂-C kg^-1 soil) followed by the rice husk treatment (1 090 mg CO₂-C kg^-1 soil); the lowest amount (150 mg CO₂-C kg^-1 soil) was observed in the aged rice husk biochar treatment. Similarly, for the old alluvial soil (farmland soil), the highest absolute cumulative CO₂-C evolution (1 290 mg CO₂-C kg^-1 soil) was observed in the sugarcane bagasse treatment and then in the rice husk treatment (1 270 mg CO₂-C kg^-1 soil); the lowest amount (200 mg CO₂-C kg^-1 soil) was in the aged rice husk biochar treatment. Aged sugarcane bagasse and rice husk biochar treatments reduced absolute cumulative CO₂-C evolution by 10% and 36%, respectively, compared with unamended recent alluvial soil, and by 10% and 18%, respectively, compared with unamended old alluvial soil. Both absolute and normalized C mineralization were similar between the sugarcane bagasse and rice husk treatments, between the biochar treatments, and between the aged biochar treatments. In both soils, the feedstock treatments resulted in the highest cumulative CO₂-C evolution, followed by the biochar treatments and then the aged biochar treatments. The absolute and normalized CO₂-C evolution and the mineralization rate constant of the stable C pool (K_s) were lower in the recent alluvial soil compared with those in the old alluvial soil. The biochars and aged biochars had a negative priming effect in both soils, but the effect was more prominent in the recent alluvial soil. These results would have good implications for improving organic matter content in organic C-poor alluvial soils.     

Transformation of 15N-labelled leguminous plant material in three contrasting soils

Summary Two soils from Pakistan (Hafizabad silt loam and Khurrarianwala silt loam) and one from Illinois, USA (Drummer silty clay loam) were incubated with ¹⁵N-labelled soybean tops for up to 20 weeks at 30°C. Mineralization of soybean ¹⁵N was slightly more rapid in the Pakistani soils, and after 20 weeks of incubation, 50%, 53%, and 56% of the applied ¹⁵N was accounted for as (NH₄ ⁺+NO₃ ^–)-N in Drummer, Hafizabad, and Khurrarianwala soils, respectively. Potentially mineralizable N (determined by anaerobic incubation) varied between 1.5% and 10% of the applied ¹⁵N in the three soils at different stages of incubation; somewhat higher percentages were mineralizable in the Pakistani soils than in the Drummer soil. From 3.7% to 9% of the applied ¹⁵N was accounted for in the microbial biomass. From 10% to 32% of the applied N was recovered in the humic acid and fulvic acid fractions of the organic matter by sequential extraction with Na₄P₂O₇ and NaOH; from 12% to 49% was recovered in the humin fraction. Of the three soils, Drummer soil contained more ¹⁵N as humic and fulvic acids. In all cases, the ¹⁵N was approximately equally distributed between the humic and fulvic acid fractions. A significant percentage of the humin ¹⁵N (52%–78%, equivalent to 8%–34% of the applied ¹⁵N) occurred in non-hydrolyzable (6 N HCl) forms. Of the hydrolyzable ¹⁵N, 42%–51% was accounted for as amino acid-N followed in order by NH₃ (17%–30%), hydrolyzable unknown forms (20%–22%), and amino sugars (6%–2%). The recovery of applied ¹⁵N for the different incubation stages was 87±22%. Recovery was lowest with the Khurrarianwala soil, presumably because of NH₃ volatilization losses caused by the high pH of this soil.     

Comparison of Chemical Methods for Assessing Nitrogen Mineralization in Two Calcareous Soils Treated with Organic Materials

Reliable and quick methods for measuring nitrogen (N)–supplying capacities of soils (NSC) are a prerequisite for using N fertilizers. This study was conducted to develop a routine method for estimation of mineralizable N in two calcareous soils (sandy loam and clay soils) treated with municipal waste compost or sheep manure. The methods used were anaerobic biological N mineralization, mineral N released by 2 M potassium chloride (KCl), ammonium (NH₄ ⁺) N extracted by 1 N sulfuric acid (H₂SO₄), NH₄ ⁺-N extracted by acid potassium permanganate (KMnO₄), and NH₄ ⁺-N released by oxidation of soil organic matter using acidified potassium permanganate. The results showed that oxidizable N extracted by acid permanganate, a simple and rapid measure of soil N availability, was correlated with results of the anaerobic method. Oxidative 0.05 N KMnO₄ was the best method, accounting for 78.4% of variation in NSC. Also, the amount of mineralized N increased with increasing level of organic materials and was greater in clay soil than sandy loam soil.     

Winter cover cropping influence on nitrogen mineralization,presidedress soil nitrate test,and corn yields

The mineralization and availability of cover crop N to the succeeding crop are critical components in the management of soil N to reduce N leaching. The effects of several leguminous and non-leguminous cover crops on soil N availability, N mineralization potential, and corn (Zea mays L.) yield were examined. The cover crops had variable effects on soil N availability and corn yield and N uptake. Because of the rapid mineralization of the cover crops following incorporation, the inorganic N levels in the soil sampled in mid-May 1992 (4 weeks after incorporation of cover crops), rather than the potentially mineralizable N, rate constants, initial potential mineralization rate, or cumulative N mineralized over 14 weeks, correlated well with N concentrations, C:N ratios, or the N added in the cover crops. However, the inclusion of potentially mineralizable N with inorganic N in a multiple regression improved the variability in the corn yield and the N uptake accounted for. Since extensive mineralization had occurred before the 21 May sampling, the potentially mineralizable N was affected more by the soil organic N and C than by the N concentrations of the cover crops. The presidedress NO₃ ^--N test levels were well predicted by the inorganic and potentially mineralizable N (R ²=0.89, P<0.01), although the test levels were better in predicting corn yield and N uptake. If the available soil N test needs to be made earlier than recommended by the presidedress NO₃ ^--N test, both inorganic and potentially mineralizable N are needed to better predict the corn yield and N uptake in the soils.