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1.
Flooding an extremely alkaline（pH 10.6） saline soil of the former Lake Texcoco to reduce salinity will affect the soil carbon（C）and nitrogen（N） dynamics.A laboratory incubation experiment was done to investigate how decreasing soil salt content affected dynamics of C and N in an extremely alkaline saline soil.Sieved soil with electrical conductivity（EC） of 59.2 dS m-1 was packed in columns,and then flooded with tap water,drained freely and conditioned aerobically at 50%water holding capacity for a month.This process of flooding-drainage-conditioning was repeated eight times.The original soil and the soil that had undergone one,two,four and eight flooding-drainage-conditioning cycles were amended with 1000 mg glucose-14C kg-1 soil and 200 mg NH4+-N kg-1soil,and then incubated for 28 d.The CO2 emissions,soil microbial biomass,and soil ammonium（NE4+）,nitrite（NO2-） and nitrate（NO3-） were monitored in the aerobic incubation of 28 d.The soil EC decreased from 59.2 to 1.0 dS m1 after eight floodings,and soil pH decreased from 10.6 to 9.6.Of the added 14C-labelled glucose,only 8%was mineralized in the original soil,while 24%in the soil flooded eight times during the 28-d incubation.The priming effect was on average 278 mg C kg-1 soil after the 28-d incubation.Soil microbial biomass C(mean 66 mg C kg-1 soil) did not change with flooding times in the unamended soil,and increased 1.4 times in the glucose-NH4+-amended soil.Ammonium immobilization and NO2- concentration in the aerobically incubated soil decreased with increasing flooding times,while NO3- concentration increased.It was found that flooding the Texcoco soil decreased the EC sharply,increased mineralization of glucose,stimulated nitrification,and reduced immobilization of inorganic N,but did not affect soil microbial biomass C.  相似文献   

2.
The contribution of bacteria and fungi to NH4+ and organic N (Norg) oxidation was determined in a grassland soil (pH 6.3) by using the general bacterial inhibitor streptomycin or the fungal inhibitor cycloheximide in a laboratory incubation study at 20°C. Each inhibitor was applied at a rate of 3 mg g?1 oven‐dry soil. The size and enrichment of the mineral N pools from differentially (NH415NO3 and 15NH4NO3) and doubly labelled (15NH415NO3) NH4NO3 were measured at 3, 6, 12, 24, 48, 72, 96 and 120 hours after N addition. Labelled N was applied to each treatment, to supply NH4+‐N and NO3?‐N at 3.15 μmol N g?1 oven‐dry soil. The N treatments were enriched to 60 atom % excess in 15N and acetate was added at 100 μmol C g?1 oven‐dry soil, to provide a readily available carbon source. The oxidation rates of NH4+ and Norg were analysed separately for each inhibitor treatment with a 15N tracing model. In the absence of inhibitors, the rates of NH4+ oxidation and organic N oxidation were 0.0045 μmol N g?1 hour?1 and 0.0023 μmol N g?1 hour?1, respectively. Streptomycin had no effect on nitrification but cycloheximide inhibited the oxidation of NH4+ by 89% and the oxidation of organic N by more than 30%. The current study provides evidence to suggest that nitrification in grassland soil is carried out by fungi and that they can simultaneously oxidize NH4+ and organic N.  相似文献   

3.
The availability of C and N to the soil microbial biomass is an important determinant of the rates of soil N transformations. Here, we present evidence that changes in C and N availability affect the 15N natural abundance of the microbial biomass relative to other soil N pools. We analysed the 15N natural abundance signature of the chloroform‐labile, extractable, NO3–, NH4+ and soil total N pools across a cattle manure gradient associated with a water reservoir in semiarid, high‐desert grassland. High levels of C and N in soil total, extractable, NO3–, NH4+ and chloroform‐labile fractions were found close to the reservoir. The δ15N value of chloroform‐labile N was similar to that of extractable (organic + inorganic) N and NO3– at greater C availability close to the reservoir, but was 15N‐enriched relative to these N‐pools at lesser C availability farther away. Possible mechanisms for this variable 15N‐enrichment include isotope fractionation during N assimilation and dissimilation, and changes in substrate use from a less to a more 15N‐enriched substrate with decreasing C availability.  相似文献   

4.
The mineralization of native soil organic matter and the simultaneous diffusion of zero NH+4 and NO?3 to a solution sink of zero N concentration was analysed experimentally and theoretically for a fine sandy loam soil. Experimentally, the NH4 and NO3 ions produced in an incubated unsaturated soil column were allowed to diffuse through a sintered glass plate into a stirred solution sink. The distribution of NH+4 and NO?3 in the soil column was measured after various incubation times. The rate of ammonification was measured directly during incubation and the rate of nitrification modelled from nitrifier growth kinetics. A Freundlich equation was used to describe the equilibrium between soluble and exchangeable NH+4 in the soil. Terms for the microbial transformation of N and the adsorption-desorption of NH+4 were combined with diffusion equations which were solved numerically using finite difference methods. The model constructed was used to predict the NH+4 and NO?3 con-centration distributions in the soil column, and good agreement was obtained between the experimental and predicted concentration profiles. The use of the model for predicting the diffusive flux of mineral N to the outer surfaces of soil peds, where it is vulnerable to leaching, was demonstrated.  相似文献   

5.
《Applied soil ecology》2010,46(3):225-231
There are plans to vegetate soil of the former lake Texcoco and use wastewater sludge to provide nutrients. However, the Texcoco soil is N depleted, so the amount of N available to the vegetation might be limited and the dynamics of C and N affected. We investigated how emissions of CO2, N2O and N2, and dynamics of mineral N were affected when different types of N fertilizer, i.e. NH4+, NO3−, or unsterilized or sterilized wastewater sludge, were added to the Texcoco soil. An agricultural soil served as control. Sewage sludge added to an alkaline saline soil (Texcoco soil) induced a decrease in concentrations of NH4+ and NO3−. Addition of sewage sludge increased the CO2 emission rate > two times compared to soil amended with sterilized sludge. The NH4+ concentration was lower when sludge was added to an agricultural soil for the first 28 days and in the Texcoco soil for 56 days compared to soil amended with sterilized sludge. Production of N2O in the agricultural soil was mainly due to nitrification, even when sludge was added, but denitrification was the main source of N2O in the Texcoco soil. Microorganisms in the sludge reduced N2O to N2, but not the soil microorganisms. It was found that microorganisms added with the sludge accelerated organic material decomposition, increased NH4+ immobilization, and induced immobilization of NO3− (in Texcoco soil). These results suggest that wastewater sludge improves soil fertility at Otumba (an agricultural soil) and would favour the vegetation of the Texcoco soil (alkaline saline).  相似文献   

6.
Zeolitites (ZTs) are rocks containing more than 50% of zeolite minerals and are known to be a suitable material for agricultural purposes by improving soil physicochemical properties and nitrogen (N) use efficiency. However, little is known about their effects on soil microbial biomass. This study aimed to evaluate short-term effects of different chabazite-rich ZT (CHAZT) amendments on soil microbial biomass and activity. A silty-clay agricultural soil was amended in three different ways, including the addition of natural (5% and 15%) and NH_4~+-enriched (10%) CHAZT. Soil dissolved organic carbon (C), total dissolved N, NH_4~+, NO_3~-, NO_2~-, microbial biomass C and N, and ergosterol were measured periodically over 16 d in a laboratory incubation. To verify the microbial immobilization of the N derived from NH_4~+-enriched CHAZT, a high15N source was used for enriching the mineral to measure the microbial biomass δ15N signature. An increase in the ergosterol content was observed in the soil amended with 5% natural CHAZT. However, no similar result was observed in the soil amended with 15% natural CHAZT, suggesting that the fungal biomass was favored at a lower CHAZT application rate. In the soil amended with NH+ 4-enriched CHAZT, microbial biomass N was related to NO_3~-production over time and inversely related to NH_4~+, suggesting high nitrification process. Isotopic measurements on microbial biomass confirmed immediate assimilation of N derived from NH_4~+-enriched CHAZT. These results suggested that the NH_4~+-enriched CHAZT used in this study supplied an immediately available N pool to the microbial biomass.  相似文献   

7.
An incubation experiment was conducted to study the response to sodium chloride (NaCl) salinity of microbial population immobilizing NH4+- and NO3−-N using glucose as an easily oxidizable C source. Immobilization of NH4+-N was faster than that of NO3−-N and was complete within 12 h of -incubation. Presence of NaCl retarded the process of N immobilization; that of NO3−-N being more affected. Remineralization of immobilized N started within 48 h in case of both NH4+- and NO3−-N and was faster for the latter. Both remineralization and nitrification were significantly delayed in the presence of NaCl; inhibition being more at 4000 mg NaCl kg−1 soil. The inhibitory effect of NaCl on remineralization of N was relatively more for NH4+-treated soil. The results of the study suggested a higher sensitivity to NaCl of microorganisms assimilating NO3−. However, remineralization of N from NO3−-assimilating microbial population was less affected by NaCl salinity compared to NH4+-assimilating population.  相似文献   

8.
To evaluate the pathways and dynamics of inorganic nitrogen (N) deposition in previously N-limited ecosystems, field additions of 15N tracers were conducted in two mountain ecosystems, a forest dominated by Norway spruce (Picea abies) and a nearby meadow, at the Alptal research site in central Switzerland. This site is moderately impacted by N from agricultural and combustion sources, with a bulk atmospheric deposition of 12 kg N ha−1 y−1 equally divided between NH4+ and NO3−. Pulses of 15NH4+ and 15NO3− were applied separately as tracers on plots of 2.25 m2. Several ecosystem pools were sampled at short to longer-term intervals (from a few hours to 1 year), above and belowground biomass (excluding trees), litter layer, soil LF horizon (approx. 5-0 cm), A horizon (approx. 0-5 cm) and gleyic B horizon (5-20 cm). Furthermore, extractable inorganic N, and microbial N pools were analysed in the LF and A horizons. Tracer recovery patterns were quite similar in both ecosystems, with most of the tracer retained in the soil pool. At the short-term (up to 1 week), up to 16% of both tracers remained extractable or entered the microbial biomass. However, up to 30% of the added 15NO3− was immobilised just after 1 h, and probably chemically bound to soil organic matter. 16% of the NH4+ tracer was also immobilised within hours, but it is not clear how much was bound to soil organic matter or fixed between layers of illite-type clay. While the extractable and microbial pools lost 15N over time, a long-term increase in 15N was measured in the roots. Otherwise, differences in recovery a few hours after labelling and 1 year later were surprisingly small. Overall, more NO3− tracer than NH4+ tracer was recovered in the soil. This was due to a strong aboveground uptake of the deposited NH4+ by the ground vegetation, especially by mosses.  相似文献   

9.
The isotope dilution method for measuring gross rates of N mineralization, immobilization, and nitrification was applied to intact soil cores so that the effects of soil mixing were avoided. Soil cores were injected with solutions of either 15NH4+ or 15NO4?; gross mineralization rates were calculated from the decline in “N enrichment of the NH: pool during a 24-h incubation; gross nitrification rates were calculated from the decline in 15N enrichment of the NO?3 pool; gross rates of NH4+ and NO3? consumption were calculated from disappearance of the 15N label. The assumptions required for application of this method to intact cores are evaluated. Sensitivity analysis revealed that homogeneous mixing of added “N with ambient pools was not a necessary assumption but that bias in distribution of added label, coincident with a non-random distribution of microbial processes, would cause significant errors in rate estimates. Rate estimates were also sensitive to errors in initial 15N and 14N pool size estimates, In a silt loam soil from a grassland site, abiotic processes consumed over 30% of the added 15NH4+ within minutes of adding the label to sterilized soil. Extracting a subset of soil cores at the beginning of an incubation is recommended for obtaining initial pool size estimates. Gross immobilization is probably stimulated by addition of inorganic 15N substrate and, therefore, is overestimated by the isotope dilution method. As an alternative method, a non-linear equation is given for calculating the gross immobilization rate from the appearance of 15N in chloroform-labile microbial biomass; but incomplete extraction of biomass N may result in low estimates. Details of the isotope dilution methodology (injection rates, concentrations, experimental artefacts, etc.) are described and discussed. When care is taken to understand the underlying assumptions and sources of error, the isotope dilution method provides a powerful tool for measuring gross rates of microbial transformations of soil nitrogen in intact soil cores.  相似文献   

10.
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.  相似文献   

11.
The soil of the former lake Texcoco is an ‘extreme’ alkaline saline soil with pH > 10 and electrolytic conductivity (EC) > 150 dS m−1. These conditions have created a unique environment. Application of wastewater sludge to Texcoco soil showed that large amounts of NH4+ were immobilized, NO3− was reduced aerobically, NO2− was formed and the mineralization of the organic material in the sludge was inhibited. A series of experiments were initiated to study the processes that inhibited the decomposition of organic material and affected the dynamics of mineral N. The large EC and pH inhibited the decomposition of easily decomposable organic material such as glucose and maize, although cellulolytic activity was observed in soil with pH 9.8 and EC 32.7 dS m−1. The high soil pH favoured NH3 volatilization of approximately 50 mg N kg−1 soil within a day and a similar amount could be fixed on the soil matrix due to the dispersed minerals and their volcanic origin. Soil microorganisms immobilized large amounts of NH4+ within a day when glucose was added to soil in excess of what was required for metabolic activity. Removal of NO3− from soil amended with glucose was not inhibited by 100% O2 and NH4+ indicating that the contribution of denitrification and assimilatory reduction to the reduction of NO3− was minimal while the formation of NO2− was not inhibited by 0.1% acetylene, known to inhibit nitrification. Additionally, the reduction of NO3− in the glucose-amended alkaline saline Texcoco soil was followed by an increase in the amount of NH4+, which could not be due to denitrification. It was concluded that the reduction of NO3− and the formation of NO2− and NH4+ in the glucose-amended soil was a result of aerobic NO3− reduction. A phylogenetic analysis of the archaeal community in the soil of the former lake Texcoco showed that some of the clones identified were capable of reducing NO3− aerobically to NO2− when glucose was added. A study of the diversity of the bacterial dissimilatory and respiratory nitrate-reducing communities indicated that bacteria could have contributed to the process.  相似文献   

12.
Rapid nitrogen（N） transformations and losses occur in the rice rhizosphere through root uptake and microbial activities. However,the relationships between rice roots and rhizosphere microbes for N utilization are still unclear. We analyzed different N forms（NH＋4,NO-3, and dissolved organic N）, microbial biomass N and C, dissolved organic C, CH4 and N2O emissions, and abundance of microbial functional genes in both rhizosphere and bulk soils after 37-d rice growth in a greenhouse pot experiment. Results showed that the dissolved organic C was significantly higher in the rhizosphere soil than in the non-rhizosphere bulk soil, but microbial biomass C showed no significant difference. The concentrations of NH＋4, dissolved organic N, and microbial biomass N in the rhizosphere soil were significantly lower than those of the bulk soil, whereas NO-3in the rhizosphere soil was comparable to that in the bulk soil. The CH4 and N2O fluxes from the rhizosphere soil were much higher than those from the bulk soil. Real-time polymerase chain reaction analysis showed that the abundance of seven selected genes, bacterial and archaeal 16 S rRNA genes, amoA genes of ammonia-oxidizing archaea and ammonia-oxidizing bacteria, nosZ gene, mcrA gene, and pmoA gene, was lower in the rhizosphere soil than in the bulk soil, which is contrary to the results of previous studies. The lower concentration of N in the rhizosphere soil indicated that the competition for N in the rhizosphere soil was very strong, thus having a negative effect on the numbers of microbes. We concluded that when N was limiting, the growth of rhizosphere microorganisms depended on their competitive abilities with rice roots for N.  相似文献   

13.
ABSTRACT

Plant nitrogen (N)-acquisition strategy affects soil N availability, community structure, and vegetation productivity. Cultivated grasslands are widely established to improve degraded pastures, but little information is available to evaluate the link between N uptake preference and forage crop biomass. Here an in-situ 15N labeling experiment was conducted in the four cultivated grasslands of Inner Mongolia, including two dicots (Medicago sativa and Brassica campestris) and two monocots (Bromus inermis and Leymus chinensis). Plant N uptake rate, shoot- and root biomass, and concentrations of soil inorganic-N and microbial biomass-N were measured. The results showed that the root/shoot ratios of the dicots were 2.6 to 16.4 fold those of the monocots. The shoot N concentrations of the dicots or legumes were 40.6% to 165% higher than those of the monocots or non-legumes. The four forage crops in the cultivated grassland preferred to uptake more NO3?-N than NH4+-N regardless of growth stages, and the NH4+/NO3? uptake ratios were significantly lower in the non-legumes than in the legumes (p < 0.05). Significant differences in the NH4+-N rather than NO3?-N uptake rate were observed among the four forages, related to plant functional types and growth stages. The NH4+ uptake rate in the perennial forages exponentially decreased with the increases in shoot-, root biomass, and root/shoot ratio. Also, the plant NH4+/NO3? uptake ratio was positively correlated with soil NH4+/NO3? ratio. Our results suggest that the major forage crops prefer to absorb soil NO3?-N, depending on soil inorganic N composition and belowground C allocation. The preferential uptake of NO3?-N by forages indicates that nitrate-N fertilizer could have a higher promotion on productivity than ammonium-N fertilizer in the semi-arid cultivated grassland.  相似文献   

14.
Field experiments were conducted to determine the effect of nitrogen (N) fertilizer forms and doses on wheat (Triticum aestivum L.) on three soils differing in their ammonium (NH4) fixation capacity [high = 161 mg fixed NH4-N kg?1 soil, medium = 31.5 mg fixed NH4-N kg?1 soil and no = nearly no fixed NH4-N kg?1 soil]. On high NH4+ fixing soil, 80 kg N ha?1 Urea+ ammonium nitrate [NH4NO3] or 240 kg N ha?1 ammonium sulfate [(NH4)2SO4]+(NH4)2SO4, was required to obtain the maximum yield. Urea + NH4NO3 generally showed the highest significance in respect to the agronomic efficiency of N fertilizers. In the non NH4+ fixing soil, 80 kg N ha?1 urea+NH4NO3 was enough to obtain high grain yield. The agronomic efficiency of N fertilizers was generally higher in the non NH4+ fixing soil than in the others. Grain protein was highly affected by NH4+ fixation capacities and N doses. Harvest index was affected by the NH4+ fixation capacity at the 1% significance level.  相似文献   

15.
This paper studies the effect of large- and small-scale changes of soil temperature and humidity on soil microbial biomass C and N, ergosterol, carbon utilization potential, organic and inorganic N and rate of C and N mineralization at 25°C. Large-scale variations are identified with seasonal changes in temperature and humidity. To simulate small-scale changes, soil temperature and humidity were manipulated in the field. The treatment resulted in damping of temperature fluctuations and a decrease of soil humidity.The majority of the studied variables exhibit pronounced seasonality, showing a clear-cut distinction between summer (July–August) and winter (December). In summer, C mineralization rate and carbon utilization potential was high but microbial and fungal biomass (ergosterol) was low.C and N mineralization rate and microbial and fungal biomass were only affected by sampling date, demonstrating that gross parameters of biomass and activity of microorganisms are not affected by small-scale changes in temperature and humidity. In contrast, variables relating to N availability (organic N, NH4+ and NO3−, microbial biomass N) and carbon utilization potential of the microbial community were highly affected by small-scale changes in soil abiotic conditions. The results suggest that changes in N dynamics induced by small-scale changes of temperature and humidity are caused by shifts in the structure of the microbial community rather than by variations in microbial biomass.  相似文献   

16.
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.  相似文献   

17.
 Gross N mineralization and nitrification rates and their relationships to microbial biomass C and N and enzyme (protease, deaminase and urease) activities were determined in soils treated with dairy shed effluent (DSE) or NH4 + fertilizer (NH4Cl) at a rate equivalent to 200 kg N ha–1 at three water potentials (0, –10 and –80 kPa) at 20  °C using a closed incubation technique. After 8, 16, 30, 45, 60 and 90 days of incubation, sub-samples of soil were removed to determine gross N mineralization and nitrification rates, enzyme activities, microbial biomass C and N, and NH4 + and NO3 – concentrations. The addition of DSE to the soil resulted in significantly higher gross N mineralization rates (7.0–1.7 μg N g–1 soil day–1) than in the control (3.8–1.2 μg N g–1 soil day–1), particularly during the first 16 days of incubation. This increase in gross mineralization rate occurred because of the presence of readily mineralizable organic substrates with low C : N ratios, and stimulated soil microbial and enzymatic activities by the organic C and nutrients in the DSE. The addition of NH4Cl did not increase the gross N mineralization rate, probably because of the lack of readily available organic C and/or a possible adverse effect of the high NH4 + concentration on microbial activity. However, nitrification rates were highest in the NH4Cl-treated soil, followed by DSE-treated soil and then the control. Soil microbial biomass, protease, deaminase and urease activities were significantly increased immediately after the addition of DSE and then declined gradually with time. The increased soil microbial biomass was probably due to the increased available C substrate and nutrients stimulating soil microbial growth, and this in turn resulted in higher enzyme activities. NH4Cl had a minimal impact on the soil microbial biomass and enzyme activities, possibly because of the lack of readily available C substrates. The optimum soil water potential for gross N mineralization and nitrification rates, microbial and enzyme activities was –10 kPa compared with –80 kPa and 0 kPa. Gross N mineralization rates were positively correlated with soil microbial biomass N and protease and urease activities in the DSE-treated soil, but no such correlations were found in the NH4Cl-treated soil. The enzyme activities were also positively correlated with each other and with soil microbial biomass C and N. The forms of N and the different water potentials had a significant effect on the correlation coefficients. Stepwise regression analysis showed that protease was the variable that most frequently accounted for the variations of gross N mineralization rate when included in the equation, and has the potential to be used as one of the predictors for N mineralization. Received: 10 March 1998  相似文献   

18.
Abstract

The rate and timing of manure application when used as nitrogen (N) fertilizer depend on N‐releasing capacity (mineralization) of manures. A soil incubation study was undertaken to establish relative potential rates of mineralization of three organic manures to estimate the value of manure as N fertilizer. Surface soil samples of 0–15 cm were collected and amended with cattle manure (CM), sheep manure (SM), and poultry manure (PM) at a rate equivalent to 200 mg N kg?1 soil. Soil without any amendment was used as a check (control). Nitrogen‐release potential of organic manures was determined by measuring changes in total mineral N [ammonium‐N+nitrate‐N (NH4 +–N+NO3 ?–N)], NH4 +–N, and accumulation of NO3 ?–N periodically over 120 days. Results indicated that the control soil (without any amendment) released a maximum of 33 mg N kg?1soil at day 90, a fourfold increase (significant) over initial concentration, indicating that soil had substantial potential for mineralization. Soil with CM, SM, and PM released a maximum of 50, 40, and 52 mg N kg?1 soil, respectively. Addition of organic manures (i.e., CM, SM, and PM) increased net N released by 42, 25, and 43% over the control (average). No significant differences were observed among manures. Net mineralization of organic N was observed for all manures, and the net rates varied between 0.01 and 0.74 mg N kg?1 soil day?1. Net N released, as percent of organic N added, was 9, 10, and 8% for CM, SM, and PM. Four phases of mineralization were observed; initial rapid release phase in 10–20 days followed by slow phase in 30–40 days, a maximum mineralization in 55–90 days, and finally a declined phase in 120 days. Accumulation of NO3 ?–N was 13.2, 10.6, and 14.6 mg kg?1 soil relative to 7.4 mg NO3 ?–N kg?1 in the control soil, indicating that manures accumulated NO3 ?–N almost double than the control. The proportion of total mineral N to NO3 ?–N revealed that a total of 44–61% of mineral N is converted into NO3 ?–N, indicating that nitrifiers were unable to completely oxidize the available NH4 +. The net rates of mineralization were highest during the initial 10–20 days, showing that application of manures 1–2 months before sowing generally practiced in the field may cause a substantial loss of mineralized N. The rates of mineralization and nitrification in the present study indicated that release of inorganic N from the organic pool of manures was very low; therefore, manures have a low N fertilizer effect in our conditions.  相似文献   

19.
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.  相似文献   

20.
Soils stored in stockpiles during opencast mining operations accumulate significant quantities of ammonium (of the order of 200 μg NH4+-N g?1 soil) within the predominantly anaerobic cores of mounds. Upon stockpile dismantling and land restoration, this NH+4-N is rapidly oxidized to NO?3-N, which is readily lost from newly restored soil ecosystems by leaching and denitrification. Experiments were set up to examine how these significant reserves of mineral N might be conserved in such situations. Application of the nitrification inhibitor dicyandiamide was successful in minimizing NO3?-N lost by leaching, though large concentrations of NH4+-N were detected in drainage waters. Straw incorporation decreased nitrate leaching by up to 40%; biomass C was some 40% greater in straw-amended than in unamended soils after 14 weeks, though biomass N was similar in both. Addition of nitrogen-free organic materials (glucose, starch and cellulose) produced different results, with glucose amendment showing the greatest reduction in nitrate leaching in the short term (due to an apparent stimulation of denitrification) whereas addition of cellulose resulted in the most effective conservation of nitrogen over 14 weeks; this was due, at least in part, to uptake of mineral N by the soil microbial biomass.  相似文献   

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