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1.
The turnover of organic matter determines the availability of plant nutrients in unfertilized soils, and this applies particularly to the alkaline saline soil of the former Lake Texcoco in Mexico. We investigated the effects of alkalinity and salinity on dynamics of organic material and inorganic N added to the soil. Glucose labelled with 14C was added to soil of the former Lake Texcoco drained for different lengths of time, and dynamics of 14C, C and N were investigated with the Detran model. Soil was sampled from an undrained plot and from three drained for 1, 5 and 8 years, amended with 1000 mg 14C‐labelled glucose kg ?1 and 200 mg NH 4+‐N kg ?1, and incubated aerobically. Production of 14CO 2 and CO 2, dynamics of NH 4+, NO 2– and NO 3–, and microbial biomass 14C, C and N were monitored and simulated with the Detran model. A third stable microbial biomass fraction had to be introduced in the model to simulate the dynamics of glucose, because > 90 mg 14C kg ?1 soil persisted in the soil microbial biomass after 97 days. The observed priming effect was mostly due to an increased decay of soil organic matter, but an increased turnover of the microbial biomass C contributed somewhat to the phenomenon. The dynamics of NH 4+ and NO 3– in the NH 4+‐amended soil could not be simulated unless an immobilization of NH 4+ into the microbial biomass occurred in the first day of the incubation without an immediate incorporation of it into microbial organic material. The dynamics of C and a priming effect could be simulated satisfactorily, but the model had to be adjusted to simulate the dynamics of N when NH 4+ was added to alkaline saline soils. 相似文献
2.
Co-composting of chicken slurry and rice straw with clinoptilolite zeolite and urea as additives was conducted to determine the characteristics of a compost and their effects on controlling ammonium (NH 4+) and nitrate (NO 3?) losses from urea. Quality of the compost was assessed based on temperature, moisture content, ash, pH, electrical conductivity, carbon/nitrogen (C/N) ratio, NH 4+, NO 3?, macronutrients, heavy metals, humic acid, microbial population, germination index, and phytotoxicity test. Moisture content and C/N ratio of the compost were 43.83% and 15, respectively. Total N, humic acid, ash, NH 4+, NO 3?, phosphorus (P), calcium (Ca), magnesium (Mg), potassium (K), and sodium (Na) increased after co-composting rice straw and chicken slurry. Copper, iron (Fe), manganese (Mn), zinc (Zn), and microbial biomass of the compost were low. The germination rate of Zea mays on distilled water and Spinacia oleracea growth on peat-based growing medium (PBGM) and compost were not significantly different. Urea amended with compost reduced N loss by retaining NH 4+ and NO 3? in the soil. 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, NO 3–, NH 4+ 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, NO 3–, NH 4+ and chloroform‐labile fractions were found close to the reservoir. The δ 15N value of chloroform‐labile N was similar to that of extractable (organic + inorganic) N and NO 3– 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.
ABSTRACTPlant 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 NO 3?-N than NH 4+-N regardless of growth stages, and the NH 4+/NO 3? uptake ratios were significantly lower in the non-legumes than in the legumes (p < 0.05). Significant differences in the NH 4+-N rather than NO 3?-N uptake rate were observed among the four forages, related to plant functional types and growth stages. The NH 4+ uptake rate in the perennial forages exponentially decreased with the increases in shoot-, root biomass, and root/shoot ratio. Also, the plant NH 4+/NO 3? uptake ratio was positively correlated with soil NH 4+/NO 3? ratio. Our results suggest that the major forage crops prefer to absorb soil NO 3?-N, depending on soil inorganic N composition and belowground C allocation. The preferential uptake of NO 3?-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
5.
An incubation experiment was carried out with maize ( Zea mays L.) leaf straw to analyze the effects of mixing the residues with soil and N amendment on the decomposition process. In order to distinguish between soil effects and nitrogen effects for both the phyllospheric microorganisms already present on the surface of maize straw and soil microorganisms the N amendment was applied in two different placements: directly to the straw or to the soil. The experiment was performed in dynamic, automated microcosms for 22 days at 15 °C with 7 treatments: (1) untreated soil, (2) non-amended maize leaf straw without soil, (3) N amended maize leaf straw without soil, (4) soil mixed with maize leaf straw, (5) N amended soil, (6) N amended soil mixed with maize leaf straw, and (7) soil mixed with N amended maize leaf straw. 15NH 415NO 3 (5 at%) was added. Gas emissions (CO 2, 13CO 2 and N 2O) were continuously recorded throughout the experiment. Microbial biomass C, biomass N, ergosterol, δ 13C of soil organic C and of microbial biomass C as well as 15N in soil total N, mineral N and microbial biomass N were determined in soil samples at the end of the incubation. The CO 2 evolution rate showed a lag-phase of two days in the non-amended maize leaf straw treatment without soil, which was completely eliminated when mineral N was added. The addition of N generally increased the CO 2 evolution rate during the initial stages of maize leaf straw decomposition, but not the cumulative CO 2 production. The presence of soil caused roughly a 50% increase in cumulative CO 2 production within 22 days in the maize straw treatments due to a slower decrease of CO 2 evolution after the initial activity peak. Since there are no limitations of water or N, we suggest that soil provides a microbial community ensuring an effective succession of straw decomposing microorganisms. In the treatments where maize and soil was mixed, 75% of microbial biomass C was derived from maize. We concluded that this high contribution of maize using microbiota indicates a strong influence of organisms of phyllospheric origin to the microbial community in the soil after plant residues enter the soil. 相似文献
6.
The assumption in using the chloroform fumigation technique for microbial biomass determination is that microbes are killed or at least inactivated by the treatment. Problems associated with transformations of the N released on or during fumigation have so far only been associated with the fumigation-incubation method. A laboratory and a field study were carried out to investigate the possible N transformations during biomass determination by the fumigation-extraction method. Labelled NH 4NO 3 (either the NO 3−, NH 4+ or both pools were 15N enriched) was applied to the soil and biomass determinations made at intervals subsequently. The size and enrichment of the ammonium (NH 4+), and nitrate (NO 3−) pools were determined before and after chloroform fumigation. The 15N enrichment of the NH 4+ pool after fumigation could only be explained if immobilisation of ammonium occurred at some time during the 24 h fumigation period. The extent of this immobilisation was calculated. In addition, there was evidence that nitrification occurred during the fumigation procedure at the start of the laboratory study and throughout the field study. The laboratory and field study differed mainly in the dynamics related to NO 3− uptake and release. There was evidence for uptake of NO 3− by the microbial biomass with and without utilization. We conclude that the 15N enrichment in the microbial biomass cannot be accurately determined when N transformations and release of non-utilized N occurs during fumigation. The possible immobilisation of mineral N during fumigation will affect the magnitude of the factor used to convert measured microbial biomass N to actual microbial biomass N in soil. 相似文献
7.
Agricultural systems that receive high amounts of inorganic nitrogen (N) fertilizer in the form of either ammonium (NH 4+), nitrate (NO 3−) or a combination thereof are expected to differ in soil N transformation rates and fates of NH 4+ and NO 3−. Using 15N tracer techniques this study examines how crop plants and soil microbes vary in their ability to take up and compete for fertilizer N on a short time scale (hours to days). Single plants of barley ( Hordeum vulgare L. cv. Morex) were grown on two agricultural soils in microcosms which received either NH 4+, NO 3− or NH 4NO 3. Within each fertilizer treatment traces of 15NH 4+ and 15NO 3− were added separately. During 8 days of fertilization the fate of fertilizer 15N into plants, microbial biomass and inorganic soil N pools as well as changes in gross N transformation rates were investigated. One week after fertilization 45-80% of initially applied 15N was recovered in crop plants compared to only 1-10% in soil microbes, proving that plants were the strongest competitors for fertilizer N. In terms of N uptake soil microbes out-competed plants only during the first 4 h of N application independent of soil and fertilizer N form. Within one day microbial N uptake declined substantially, probably due to carbon limitation. In both soils, plants and soil microbes took up more NO 3− than NH 4+ independent of initially applied N form. Surprisingly, no inhibitory effect of NH 4+ on the uptake and assimilation of nitrate in both, plants and microbes, was observed, probably because fast nitrification rates led to a swift depletion of the ammonium pool. Compared to plant and microbial NH 4+ uptake rates, gross nitrification rates were 3-75-fold higher, indicating that nitrifiers were the strongest competitors for NH 4+ in both soils. The rapid conversion of NH 4+ to NO 3− and preferential use of NO 3− by soil microbes suggest that in agricultural systems with high inorganic N fertilizer inputs the soil microbial community could adapt to high concentrations of NO 3− and shift towards enhanced reliance on NO 3− for their N supply. 相似文献
8.
The contribution of bacteria and fungi to NH 4+ and organic N (N org) 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 (NH 415NO 3 and 15NH 4NO 3) and doubly labelled ( 15NH 415NO 3) NH 4NO 3 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 NH 4+‐N and NO 3?‐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 NH 4+ and N org were analysed separately for each inhibitor treatment with a 15N tracing model. In the absence of inhibitors, the rates of NH 4+ 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 NH 4+ 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 NH 4+ and organic N. 相似文献
9.
Agricultural systems that receive high or low organic matter (OM) inputs would be expected to differ in soil nitrogen (N) transformation rates and fates of ammonium (NH 4+) and nitrate (NO 3−). To compare NH 4+ availability, competition between nitrifiers and heterotrophic microorganisms for NH 4+, and microbial NO 3− assimilation in an organic vs. a conventional irrigated cropping system in the California Central Valley, chemical and biological soil assays, 15N isotope pool dilution and 15N tracer techniques were used. Potentially mineralizable N (PMN) and hot minus cold KCl-extracted NH 4+ as indicators of soil N supplying capacity were measured five times during the tomato growing season. At mid-season, rates of gross ammonification and gross nitrification after rewetting dry soil were measured in microcosms. Microbial immobilization of NO 3− and NH 4+ was estimated based on the uptake of 15N and gross consumption rates. Gross ammonification, PMN, and hot minus cold KCl-extracted NH 4+ were approximately twice as high in the organically than the conventionally managed soil. Net estimated microbial NO 3− assimilation rates were between 32 and 35% of gross nitrification rates in the conventional and between 37 and 46% in the organic system. In both soils, microbes assimilated more NO 3− than NH 4+. Heterotrophic microbes assimilated less NH 4+ than NO 3− probably because NH 4+ concentrations were low and competition by nitrifiers was apparently strong. The high OM input organic system released NH 4+ in a gradual manner and, compared to the low OM input conventional system, supported a more active microbial biomass with greater N demand that was met mainly by NO 3− immobilization. 相似文献
10.
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 15NH 4+ or 15NO 4?; 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 NH 4+ and NO 3? 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 15NH 4+ 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
11.
Abstract To determine the relationships between microbial biomass nitrogen (N), nitrate–nitrogen leaching (NO 3-N leaching) and N uptake by plants, a field experiment and a soil column experiment were conducted. In the field experiment, microbial biomass N, 0.5 mol L ?1 K 2SO 4 extractable N (extractable N), NO 3-N leaching and N uptake by corn were monitored in sawdust compost (SDC: 20 Mg ha ?1 containing 158 kg N ha ?1 of total N [approximately 50% is easily decomposable organic N]), chemical fertilizer (CF) and no fertilizer (NF) treatments from May 2000 to September 2002. In the soil column experiment, microbial biomass N, extractable N and NO 3-N leaching were monitored in soil treated with SDC (20 Mg ha ?1) + rice straw (RS) at five different application rates (0, 2.5, 5, 7.5 and 10 Mg ha ?1 containing 0, 15, 29, 44 and 59 kg N ha ?1) and in soil treated with CF in 2001. Nitrogen was applied as (NH 4) 2SO 4 at rates of 220 kg N ha ?1 for SDC and SDC + RS treatments and at a rate of 300 kg N ha ?1 for the CF treatment in both experiments. In the field experiment, microbial biomass N in the SDC treatment increased to 147 kg N ha ?1 at 7 days after treatment (DAT) and was maintained at 60–70 kg N ha ?1 after 30 days. Conversely, microbial biomass N in the CF treatment did not increase significantly. Extractable N in the surface soil increased immediately after treatment, but was found at lower levels in the SDC treatment compared to the CF treatment until 7 DAT. A small amount of NO 3-N leaching was observed until 21 DAT and increased markedly from 27 to 42 DAT in the SDC and CF treatments. Cumulative NO 3-N leaching in the CF treatment was 146 kg N ha ?1, which was equal to half of the applied N, but only 53 kg N ha ?1 in the SDC treatment. In contrast, there was no significant difference between N uptake by corn in the SDC and CF treatments. In the soil column experiment, microbial biomass N in the SDC + RS treatment at 7 DAT increased with increased RS application. Conversely, extractable N at 7 DAT and cumulative NO 3-N leaching until 42 DAT decreased with increased RS application. In both experiments, microbial biomass N was negatively correlated with extractable N at 7 DAT and cumulative NO 3-N leaching until 42 DAT, and extractable N was positively correlated with cumulative NO 3-N leaching. We concluded that microbial biomass N formation in the surface soil decreased extractable N and, consequently, contributed to decreasing NO 3-N leaching without impacting negatively on N uptake by plants. 相似文献
12.
We assessed the influence of the addition of four municipal or agricultural by-products (cotton gin waste, ground newsprint,
woodchips, or yard trimmings), combined with two sources of nitrogen (N), [ammonium nitrate (NH 4NO 3) or poultry litter] as carbon (C) sources on active bacterial, active fungal and total microbial biomass, cellulose decomposition,
potential net mineralization of soil C and N and soil nutrient status in agricultural soils. Cotton gin waste as a C source
promoted the highest potential net N mineralization and N turnover. Municipal or agricultural by-products as C sources had
no affect on active bacterial, active fungal or total microbial biomass, C turnover, or the ratio of net C:N mineralized.
Organic by-products and N additions to soil did not consistently affect C turnover rates, active bacterial, active fungal
or total microbial biomass. After 3, 6 or 9 weeks of laboratory incubation, soil amended with organic by-products plus poultry
litter resulted in higher cellulose degradation rates than soil amended with organic by-products plus NH 4NO 3. Cellulose degradation was highest when soil was amended with newsprint plus poultry litter. When soil was amended with organic
by-products plus NH 4NO 3, cellulose degradation did not differ from soil amended with only poultry litter or unamended soil. Soil amended with organic
by-products had higher concentrations of soil C than soil amended with only poultry litter or unamended soil. Soil amended
with organic by-products plus N as poultry litter generally, but not always, had higher extractable P, K, Ca, and Mg concentrations
than soil amended with poultry litter or unamende soil. Agricultural soil amended with organic by-products and N had higher
extractable N, P, K, Ca and Mg than unamended soil. Since cotton gin waste plus poultry litter resulted in higher cellulose
degradation and net N mineralization, its use may result in faster increase in soil nutrient status than the other organic
by-products and N sources that were tested.
Received: 15 May 1996 相似文献
13.
PurposeMany studies have shown the simulated effects of nitrogen (N) deposition on soil microbial community composition by adding N directly to the forest floor but have ignored the N retention process by the canopy. This study was conducted to compare the responses of soil microbial biomass and community composition between soil application of N (SAN) and foliage application of N (FAN). Materials and methodsA pot experiment was designed with (1) two N application methods (SAN and FAN), (2) three N application levels (5.6, 15.6 and 20.6 g N m?2 year?1), and (3) two tree species (Schima superba Gardn. et Champ. and Pinus massoniana Lamb.) following a nested factorial design. Soil microbial biomass and community composition were determined using phospholipid fatty acids (PLFAs) techniques after 1 and 1.5 years of treatments. Results and discussionNitrogen addition increased (P?<?0.05) soil NH4+-N content and soil NO3?-N content and decreased (P?<?0.05) soil pH and soil microbial (bacterial, fungal, and actinomycete) biomass for both N application methods. Compared with the SAN treatment, the FAN treatment had higher (P?<?0.05) pH and lower (P?<?0.05) contents of soil NH4+-N and soil NO3?-N. Soil microbial biomass and community composition were significantly different between the different N addition levels under the SAN treatment, but they showed no significant difference (P?<?0.05) between the different N addition levels under the FAN treatment. The soil microbial biomass in the S. superba soil was higher (P?<?0.05) than that in the P. massoniana soil for the FAN treatment, with the opposite trend observed under the SAN treatment. Moreover, redundancy analysis showed that soil microorganisms were significantly correlated with soil pH, soil water content, NH4+-N, and NO3?-N. ConclusionsThe results showed that N addition affected soil properties, microbial biomass, and the composition of microbial communities; however, the FAN treatment had less influence on soil properties and soil microorganisms than did the SAN treatment over short time scales, and the extent of this effect was different between coniferous and broadleaf trees. 相似文献
14.
Soils stored in stockpiles during opencast mining operations accumulate significant quantities of ammonium (of the order of 200 μg NH 4+-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 NO 3?-N lost by leaching, though large concentrations of NH 4+-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
15.
Indirect evidence of the nitrogen (N) status of tropical forests strongly suggests that in heavily weathered soils under old-growth lowland tropical forests nitrogen is in relative excess. However, within the lowland forests of the Amazon basin, there is substantial evidence that soil texture influences soil NH 4+ and NO 3? concentrations and hence possibly N availability and retention in the soil. Here, we evaluate the soil N status of two heavily weathered soils which contrast in texture (sandy versus clay Oxisol). Using 15N pool dilution, we quantified gross rates of soil N cycling and retention. We also measured the δ 15N signatures from the litter layer down to 50-cm depth mineral soil and calculated the overall 15N enrichment factor ( ε) for each soil type. The clay soil showed high gross N mineralization and nitrification rates and a high overall 15N enrichment factor, signifying high N losses. The sandy soil had low gross rates of N cycling and 15N enrichment factor, manifesting a conservative soil N cycling. Faster turnover rates of NH 4+ compared to NO 3? indicated that NH 4+ cycles faster through microorganisms than NO 3?, possibly contributing to better retention of NH 4+ than NO 3?. However this was opposite to abiotic retention processes, which showed higher conversion of NO 3? to the organic N pool than NH 4+. Our combined results suggest that clay Oxisol in Amazonian forest have higher N availability than sandy Oxisol, which will have important consequences for changes in soil N cycling and losses when projected increase in anthropogenic N deposition will occur. 相似文献
16.
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, NH 4+ and NO 3−, 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
17.
Temperate forests dominated by Quercus spp. cover large parts of Central Mexico and rural communities depend on these forests for wood and charcoal. The impacts of charcoal production on selected chemical properties including C and N dynamics, and populations of ammonifiers, nitrifiers and denitrifiers were investigated on surface soils (0–15 cm) collected during the dry and rainy season of these forests. Organic C was halved in soil at the kiln sites compared to undisturbed forest soil. Concentrations of exchangeable Ca 2+, K + and Mg 2+ increased >1.6 times at kiln sites and pH increased from 4.5 in undisturbed soil to 7.0 at kiln sites. The kiln sites had 1.3 times and 2.4 times lower microbial biomass C and N, respectively, than undisturbed forest sites during the rainy season. Although the effect of charcoal production on NH 4+, NO 2? and NO 3? concentrations was small, the ammonifying, nitrifying and denitrifiers were 16 times lower at the kiln sites than in the undisturbed forest soil. This research found that the charcoal production had a negative effect on the cultivable microorganisms involved in N cycling and the soil microbial biomass C and N compared to undisturbed forest soil. Differences in inorganic N dynamics were more affected by seasonality, i.e. precipitation, than by charcoal production. 相似文献
18.
Sodium chloride, at rates up to 100 mg g ?1, was added to a Sassafras sandy loam amended with finely-ground alfalfa to determine the effect of NaCl on CO 2 evolution, ammonification, and nitrification in a 14-week study. A NaCl concentration of 0.25 mg g ?1 significantly reduced CO 2 evolution by 16% in unamended soil and 5% in alfalfa-amended soil. Increasing NaCl progressively reduced CO 2 evolution, with no CO 2 evolved from the soil receiving 100 mg NaCl g ?1. A 0.50 mg NaCl g ?1 rate was required before a significant reduction in decomposition of the alfalfa occurred. The NO ?2-N + NO ?3-N content of the soil was significantly reduced from 40 to 37 μg g ?1 at 0 and 0.25 mg NaCl g ?1, respectively in the unamended soil. In the alfalfa amended soil, nitrification was significantly reduced at 5 mg NaCl g ?1. At 10 mg NaCl g ?1, nitrification was completely inhibited, there being only 6 and 2 μg NO ?2-N + NO ?3-N g ?1 in the alfalfa amended and unamended soil, respectively. In the alfalfa amended soil NH +4-N accumulated from 6 μg g ?1 at the 0 NaCl rate to a maximum of 54 μg g ?1 with 25 mg NaCl g ?1. These higher NH +4-N values resulted in a 0.5 unit increase in the pHw over that of the 0 NaCl rate in the alfalfa amended soil. At NaCl concentrations above 25 mg g ?1 there was a reduction in NH +4-N. The addition of alfalfa to the soil helped to alleviate the adverse affects of NaCl on CO 2 evolution and nitrification. 相似文献
19.
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 (NH 4) fixation capacity [high = 161 mg fixed NH 4-N kg ?1 soil, medium = 31.5 mg fixed NH 4-N kg ?1 soil and no = nearly no fixed NH 4-N kg ?1 soil]. On high NH 4+ fixing soil, 80 kg N ha ?1 Urea+ ammonium nitrate [NH 4NO 3] or 240 kg N ha ?1 ammonium sulfate [(NH 4) 2SO 4]+(NH 4) 2SO 4, was required to obtain the maximum yield. Urea + NH 4NO 3 generally showed the highest significance in respect to the agronomic efficiency of N fertilizers. In the non NH 4+ fixing soil, 80 kg N ha ?1 urea+NH 4NO 3 was enough to obtain high grain yield. The agronomic efficiency of N fertilizers was generally higher in the non NH 4+ fixing soil than in the others. Grain protein was highly affected by NH 4+ fixation capacities and N doses. Harvest index was affected by the NH 4+ fixation capacity at the 1% significance level. 相似文献
20.
Short-term metabolic activities, including ammonincation, nitrification, denitrification and the release of CO 2, with and without added substrate, and most probable numbers of ammonifiers, nitrifiers and denitrifiers were measured on stored topsoil from pasture over 140 days in the absence of growing plants. Parallel samples of irradiated and untreated soil were examined. Release of mineral-N, chiefly as NH +4N, was greater from the irradiated soil. In the untreated soil there was a slight increase in NO 3?N. Microorganisms (estimated by MPN method) and microbial respiration in the untreated soil increased, and then diminished with time.The release of 13N 2O and 13N 2 was measured from intact soil cores amended with 13NO 3?N and 13NH +4N. The principal product from the treated soil when 13NO 3?N was added was 13N 2, with little 13N 2O, whereas the irradiated soil evolved both 13N 2 and 13N 2O. Similarly, the irradiated soil continuously evolved 13N 2O from 13NH +4N in contrast to the untreated soil. 相似文献
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