Relationships between microbial biomass nitrogen,nitrate leaching and nitrogen uptake by corn in a compost and chemical fertilizer-amended regosol

Abstract

To determine the relationships between microbial biomass nitrogen (N), nitrate–nitrogen leaching (NO₃-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 K₂SO₄ extractable N (extractable N), NO₃-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 NO₃-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 (NH₄)₂SO₄ 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 NO₃-N leaching was observed until 21 DAT and increased markedly from 27 to 42 DAT in the SDC and CF treatments. Cumulative NO₃-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 NO₃-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 NO₃-N leaching until 42 DAT, and extractable N was positively correlated with cumulative NO₃-N leaching. We concluded that microbial biomass N formation in the surface soil decreased extractable N and, consequently, contributed to decreasing NO₃-N leaching without impacting negatively on N uptake by plants.     

灌溉施用氮肥后氮素在土壤中的转化及淋失状况: 土柱模拟研究

A soil column method was used to compare the effect of drip fertigation (the application of fertilizer through drip irrigation systems, DFI) on the leaching loss and transformation of urea-N in soil with that of surface fertilization combined with flood irrigation (SFI), and to study the leaching loss and transformation of three kinds of nitrogen fertilizers (nitrate fertilizer, ammonium fertilizer, and urea fertilizer) in two contrasting soils after the fertigation. In comparison to SFI, DFI decreased leaching loss of urea-N from the soil and increased the mineral N (NH₄⁺-N + NO₃^--N) in the soil. The N leached from a clay loam soil ranged from 5.7% to 9.6% of the total N added as fertilizer, whereas for a sandy loam soil they ranged between 16.2% and 30.4%. Leaching losses of mineral N were higher when nitrate fertilizer was used compared to urea or ammonium fertilizer. Compared to the control (without urea addition), on the first day when soils were fertigated with urea, there were increases in NH₄⁺-N in the soils. This confirmed the rapid hydrolysis of urea in soil during fertigation. NH₄⁺-N in soils reached a peak about 5 days after fertigation, and due to nitrification it began to decrease at day 10. After applying NH₄⁺-N fertilizer and urea and during the incubation period, the mineral nitrogen in the soil decreased. This may be related to the occurrence of NH₄⁺-N fixation or volatilization in the soil during the fertigation process.     

Leaching Methods Can Underestimate Mineralization Potential of Soils

Aerobic incubations to estimate net nitrogen (N) mineralization typically involve periodic leaching of soil with 0.01 M calcium chloride (CaCl₂), so as to remove mineral N that would otherwise be subject to immobilization. A study was conducted to evaluate the accuracy of leaching for analysis of exchangeable ammonium (NH₄⁺)-N and nitrate + nitrite (NO₃^?+ NO₂^–)-N, relative to conventional extractions using 2 M potassium chloride (KCl). Ten air-dried soils were used, five each from Illinois and Brazil, that had been amended with NH₄⁺-N (1 g kg^?1) and NO₃^–-N (0.6 g kg^?1). Both methods were in good agreement for inorganic N analysis of the Brazilian Oxisols, whereas leaching was significantly lower by 12–48% in recovering exchangeable NH₄⁺-N from Illinois Alfisols, Mollisols, and Histosols. The potential for underestimating net N mineralization was confirmed by a 12-wk incubation experiment showing 9–86% of mineral N recoveries from three temperate soils as exchangeable NH₄⁺.     

Effect of ammonium-, nitrite- and nitrate nitrogen on anaerobic nitrogenase activity in soil

Sandy loam soil, with added glucose, was incubated anaerobically under N₂ and subjected to repeated 1-h C₂H₂ reduction assays. In the presence of 1% glucose the addition of 50 μg NH₄⁺ ?N/g or of 20 μg NO^?₃ N/g (untreated soil contained 1.2 μg NH⁺₄?N and 7.10 μg NO^?₃-N/g) caused at least some suppression of nitrogenase activity. Activity developed when the KCl-extractable soil inorganic nitrogen concentration dropped below 35 μg/g. In the presence of 0.1 or 0.05% glucose the addition of 5 μg NH⁺₄?N/g caused some suppression of nitrogenase activity. However, activity developed when the soil NH₄⁺-N concentration dropped below about 4 μg/g. With 0.1% glucose and 5 μg added NO^?₂ N/g, activity did not develop until the soil NO^?₂ -N concentration dropped to zero. Added NO^?₃ N was rapidly reduced and denitrified to NO^?₂- N, N₂O-N and NH⁺₄ N and furthermore caused some inhibition of CO₂ evolution. The data from NH₄^?-addition experiments are consistent with a nitrogenase repression/ derepression threshold of 4 and 35μg NH⁺₄-N/g at 0.05 and 1% glucose concentrations, respectively. The data from NO^?₂- and NO^?₃-addition experiments suggest a combination of repression and toxicity effects in the presence of added NO^?₃ N.     

Soil inorganic nitrogen composition and plant functional type determine forage crops nitrogen uptake preference in the temperate cultivated grassland,Inner Mongolia

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.     

坡缕石包膜对尿素氮行为的影响

采用静态吸收和土柱淋溶试验方法,分析对比了3种不同用量坡缕石包膜尿素与普通尿素施入土壤后对尿素氮行为的影响,结果表明:在土壤中施用坡缕石包膜尿素较普通尿素减少10.38%～26.24%的氨挥发损失,减少5.88%～27.74%的氮素(NO3--N+NH4+-N)淋溶损失,20%的坡缕石包膜尿素能显著提高土柱土壤NH4+-N含量,3种坡缕石包膜尿素都能极显著提高土柱土壤NO3--N含量.坡缕石包膜后能减少尿素氨的挥发,降低NH4+-N和NO3--N的淋失,提高土壤NH4+-N和NO3--N含量,以20%的坡缕石包膜尿素的综合生态效应最好.     

Biodegradation of an oily waste as influenced by nitrogen forms and sources

Biodegradation rates of oily waste in soil can be limited by mineral nutrients, particularly N and P. A laboratory incubation experiment was carried out to investigate the influence of N forms, nitrate (NO^? ₃-N) vs ammonium nitrogen (NH⁺ ₄-N), and sources, i.e., the conjugate cations/anions, on C mineralization rate (CMR) was determined daily by measuring the CO₂ evolved using gas chromatography. The CMR and the cumulative C mineralized (CCM) varied with the form and/or the source of N applied. The greatest enhancement in CMR occurred in the NO^? ₃-treatments in which the source conjugate cation was Ca⁺². The addition of P fertilizer further enhanced C mineralization rates irrespective of the form and/or the source of N added. The results show that up to 45% of the added oily waste mineralized as CO₂-C in 28 d. The residual P and N (NO^? ₃-N plus NH⁺ ₄-N) data showed that approximately 90% of the added P and N were utilized for oil decomposition. The amount of residual NO^? ₃-N appeared to have an inverse relationship with CCM. The NO^? ₃-N utilization occurred at the expense of NH⁺ ₄-N and this was particularly high in the treatments which received P.     

Salinity and nitrogen mineralization in soil

A laboratory study determined the effects of salinity on ammonification, nitrification and mineral N accumulation in incubated soils. NH⁺₄-N, NO^?₂-N and NO^?₃-N were measured periodically for 102 days in unamended soil of varying salinity and in soil amended with farm compost, mustard oil cake or urea. Increased salinity progressively retarded ammonification but did not suppress it completely. Nitrification was retarded, suppressed or inhibited completely by salinity, the effect depended on both the amount of salt and the type of amendment added to the soil. The amount of mineral N that accumulated generally decreased with increased salinity.     

Leaching of nitrogen from small forest catchments having different deposition and different stores of nitrogen

This investigation describes storage and leaching dynamics of nitrogen in three small forest catchments of the Swedish Integrated Monitoring Programme (IM). The sites, situated in North and South Sweden, have similar types of boreal forests and acid podsols although some properties of the catchments are very dissimilar. Total nitrogen deposition ranges from 0.2 to 2 g m^?2 yr^?1. Reported measurements include soil stores, tree biomass, soil water and stream water chemistry. The investigated catchments only leach small amounts of nitrogen. NH₄ ⁺ and NO₃ ^? concentrations are commonly low with sudden concentration peaks. Signs of developing nitrogen saturation are clearly visible at one of the sites. These signs are a low C/N ratio, nearly 20, in the upper part of the mineral soil and an unseasonal behaviour of NH₄ ⁺ and NO₃ ^? peaks in the soil solution. Properties of the soil organic matter, which contains huge stores of nitrogen, and the timing of hydrologic events, are crucial for the future leaching losses.     

日光温室土壤剖面矿质态氮的含量、累积及其分布特性

测定了西安郊区和杨凌地区日光温室栽培番茄生长期间及收获后土壤剖面矿质态氮(铵态氮及硝态氮)的含量,分析了不同形态氮素在土壤剖面的累积及分布情况。结果表明,随着番茄的生长,土壤剖面硝态氮含量逐渐降低,降低的幅度因土壤层次不同而异;土壤剖面铵态氮以3月份含量最高,11月份与5月份相近。番茄收获后土壤剖面残留矿质氮以硝态氮为主,约占土壤剖面矿质氮的比例为80%～90%;残留的铵态氮在土壤剖面的分布相对较为一致。蔬菜生长期间及收获时日光温室土壤剖面硝态氮累积量均表现出在土壤表层相对累积现象,且温室土壤剖面硝态氮的残留量仍高于露地及高产农田。为减少硝态氮淋失带来的环境问题,除合理施用氮肥外,如何减少日光温室蔬菜作物收获后残留硝态氮的淋溶是值得进一步研究的问题。     

DENITRIFICATION IN A VERY ACID TROPICAL SOIL

In a very acid upland clay surface soil and with glucose added to give initial C/N weight ratios (added glucose-C: NO₃-N) in the soil of 0, 2 and 5, the rates of evolution of N₂ and N₂O were maximum at C/N = 2 but were significantly less at 0 and 5. The total N₂ and N₂O production was highest at C/N = 0, confirming that increasing amounts of glucose immobilised more nitrate into the biomass. As with added NO^?₃-N, the time lag, preceding a maximum ‘steady state’ rate of N₂0 evolution, increased regularly with increasing glucose. Within this ‘steady state’ period, the gaseous CO₂-C/(N₂+ N₂O)-N weight ratio in the effluent gas are between 1.0 and 1.3, which corresponds well with the stoichiometric ratios of 1.07 and 1.29 for the reduction of NO^?₃ to N₂O and N₂ respectively. Before and after this period, this gaseous C/N ratio was much higher. Denitrification was not observed in subsurface soil even after adding 100 mg kg^?1glucose-C although it contained 4 times as much indigenous nitrate as the surface soil. Inoculating this soil with increasing amounts of the surface soil, up to 15 per cent by weight, induced substantial increases in the rates and amounts of denitrification. The effects of increasing the soil pH. of introducing increasing oxygen concentrations in the influent gas. and the fate of added NH⁺₄-N, are briefly reported here. In these experiments. NO^?₂-N did not accumulate in the incubated soil nor was there any NH₃in the effluent gas. Evolution of N₂ only occurred when N₂O evolution was in its final stages.     

Short-term effects of ammonium nitrogen in upland pasture soil affected or not affected by cattle

The short-term effects of excessive NH₄⁺-N on selected characteristics of soil unaffected (low annual N inputs) and affected (high annual N inputs) by cattle were investigated under laboratory conditions. The major hypothesis tested was that above a theoretical upper limit of NH₄⁺ concentration, an excess of NH₄⁺-N does not further increase NO₃⁻ formation rate in the soil, but only supports accumulation of NO₂⁻-N and gaseous losses of N as N₂O. Soils were amended with 10 to 500 μg NH₄⁺-N g⁻¹ soil. In both soils, addition of NH₄⁺-N increased production of NO₃⁻-N until some limit. This limit was higher in cattle-affected soil than in unaffected soil. Production of N₂O increased in the whole range of amendments in both soils. At the highest level of NH₄⁺-N addition, NO₂⁻-N accumulated in cattle-affected soil while NO₃⁻-N production decreased in cattle-unaffected soil. Despite being statistically significant, observed effects of high NH₄⁺-N addition were relatively weak. Uptake of mineral N, stimulated by glucose amendment, decreased the mineral N content in both soils, but it also greatly increased production of N₂O.     

Comparative Study on Disturbed and Undisturbed Soil Sample Incubation for Estimating Soil Nitrogen-Supplying Capacity

Application of nitrogen (N) fertilizers without knowing the N-supplying capacity of soils may lead to low N use efficiency, uneconomical crop production, and pollution of the environment. Based on the results from pot experiments treated with soil initial nitrate leaching and native soil, long-term alternate leaching aerobic incubation was conducted to study the disturbed and undisturbed soil N-supplying capacity of surface soil samples in 11 sites with different fertilities on the Loess Plateau. The results indicated that the entire indexes and ryegrass (Lolium perenne) uptake N with soil initial nitrate leaching showed a better correlation than that without soil initial nitrate leaching. Except the correlation coefficients for soil initial nitrate (NO₃ ^?)-N and mineral N extracted by calcium chloride (CaCl₂) before aerobic incubation with ryegrass uptake without soil initial nitrate leaching, the correlation coefficients for soil initial NO₃ ^?-N and mineral N extracted by CaCl₂ before aerobic incubation with ryegrass uptake with soil initial nitrate leaching and those for mineralizable N extracted by aerobic incubation, soil initial mineral N and mineralizable N extracted by aerobic incubation, potentially mineralizable N (N₀) and soil initial mineral N + N₀ with ryegrass uptake N under the two cases in disturbed treatment were all higher than those in undisturbed treatment. We concluded that NO₃ ^?-N in soil extracted by CaCl₂ before aerobic incubation can reflect soil N-supplying capacity but cannot reflect soil potential N-supplying capacity. Without soil initial nitrate leaching, the effect of disturbed and undisturbed soil samples incubated under laboratory conditions for estimating soil N-supplying capacity was not good; however, with soil initial nitrate leaching, this method could give better results for soil N-supplying capacity. Based on the results from pot experiments treated with soil initial nitrate leaching and native soil, the mineralization of disturbed soil samples can give provide better results for predicting soil N-supplying capacity for in situ structure soil conditions on the Loess Plateau than undisturbed soil samples.     

Foliage application of nitrogen has less influence on soil microbial biomass and community composition than soil application of nitrogen

Purpose

Many 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 methods

A 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 discussion

Nitrogen 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.

Conclusions

The 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.

     

The potential of using 15N natural abundance in changing ammonium-N and nitrate-N pools for studying in situ soil N transformations

Purpose

This study examined the usefulness of ¹⁵N natural abundance (δ¹⁵N) with in situ core incubation to quantify the predominant N transformation processes in a natural suburban forest of subtropical Australia, which was subjected to prescribed burning.

Materials and methods

In situ core incubation for 3 days with 20 ml water, or 160.79 ml of 60 mg L^?1 NO₃^?-N surface application, and in situ core with 160.79 ml water but without incubation were set up in Toohey forest for sampling three times as before (once) and after (twice) a prescribed burning. The δ¹⁵N of NH₄⁺-N and NO₃^?-N in the top 5 cm soil before and after the incubation, and δ¹⁵N of NO₃^?-N in the 5–10 cm soil before incubation were compared with each other to examine the soil N mineralisation, nitrification, denitrification, and nitrate leaching processes.

Results and discussion

The significant decrease in δ¹⁵N of NH₄⁺-N after incubation under 20 ml water treatment was ascribed to soil N mineralisation, and the significant decrease in δ¹⁵N of NH₄⁺-N and significant increase in δ¹⁵N of NO₃^?-N after incubation with elevated water and nitrate inputs were associated with N mineralisation and nitrification, respectively, 2 months after the burning. The 160.79 ml water treatment also triggered nitrification in the baseline soil cores in both samplings after the burning. Water was crucial to stimulate soil N mineralisation and nitrification, but excessive water depleted labile N pools and reduced N mineralisation and nitrification. Burning effects were hard to separate from the seasonal impacts on soil N cycling processes.

Conclusions

The δ¹⁵N in soil mineral N pools was sensitive to indicate soil N mineralisation and nitrification processes. Soil water and labile N were determining factors for N transformations in the soil. It is suggested that δ¹⁵N combined with soil inorganic N concentrations and net N transformation rates could be used to identify primary N transformation processes. More frequent samplings would be needed to differentiate burning impacts from the seasonal impacts on soil N cycling processes.

     

Regression equations to monitor inorganic nitrogen changes in fallow and wheat soils

Soil NH⁺₄-N and NO^?₃-N at five soil depths (0–10, 10–20, 20–40, 40–60, 60–80 cm) and some environmental variables were measured in a field trial under fallow and wheat for 9 months.Significant linear and quadratic relationships were obtained relating soil NH⁺₄-N, NO^?₃-N, NH⁺₄-N + NO^?₃-N, and NH⁺₄-N + NO^?₃ + total-N uptake by wheat to soil heat accumulation (temperature), moisture, and rainfall. R² values generally decreased with soil depth and the maximum value (37%) was obtained for NO^?₃-N changes in the topsoil (0–10 cm).Although a considerable amount of variation in the inorganic values recorded is not included in the equations, our results suggest that the development of the above relationships particularly of the quadratic type are useful to predict crop requirements for N by measurement of environmental variables in the field.     

The effect of form and level of inorganic N on nitrogen use efficiency of sugarcane grown in pots

To-date, assessments of nitrogen use efficiency (NUE) of sugarcane have not included the contribution of its components, nitrogen uptake efficiency (NUpE) and nitrogen utilization efficiency (NUtE). This study determined these values, based on biomass and plant nitrogen (N) content, in two four-month-old pot-grown genotypes. The treatments included six N regimes, with nitrate (NO₃^—N) or ammonium (NH₄⁺-N) supplied alone, or as NO₃^?-N for the first 6 weeks and then NH₄⁺-N until harvest, each as 4 or 20 mM. Regardless of the N form, NUE was higher at four than at 20 mM due to significantly higher NUpE at low N supply. The results indicated that there was luxury N uptake and preference for NH₄⁺-N nutrition, which resulted in the highest determined NUE. There were significant differences between genotypes in biomass, morphological growth parameters, N uptake, total plant N and NUE, the latter matching previously established sucrose yield-based NUE field rankings.     

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

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

Soil mineral nitrogen dynamics under bare fallow and wheat in vertisols of semi-arid Mediterranean Morocco

 The evoluion of NH₄ ⁺-N and NO₃ ^–-N was monitored during three growing seasons, 1992–1993, 1993–1994, 1994–1995 in the soil profile (0–60 or 0–90 cm) under bare fallow and wheat on a vertisol site of the Sais plateau, Morocco. The aim of this study was to relate the soil mineral N dynamics to crop N uptake and soil N transformation processes. The efficacy of the current N fertilisation rate (100 kg N ha^–1) for wheat production in the region was evaluated. The high level of residual mineral N in the soil profile resulted from a low N plant uptake relative to the soil N supply and N fertilisation, and masked the effect of N fertilisation on dry matter accumulation. NH₄ ⁺-N was present in considerable amounts, suggesting a low nitrification rate under the given pedo-climatic conditions. An artefact due to the sampling procedure was encountered shortly after the application of N fertiliser. Losses through leaching and denitrification occurred after heavy rainfall, but were limited. At least part of the exchangeable NH₄ ⁺-N seemed to be barely taken up by the crop. NO₃ ^–-N was therefore considered to be a better indicator of plant-available N than total mineral N for this type of soil. The low N fertiliser use efficiencies demonstrated clearly that the current fertilisation rate (100 kg N ha^–1) for wheat production in this region is unsustainable. The maximum N uptake ranged from 40 kg N ha^–1 to 180 kg N ha^–1. The estimation of the seasonal production potential is considered to be the main prerequisite for the determination of the best rates and timing of N fertiliser application in this region. Received: 9 December 1997     

The influence of glucose and nitrate concentrations upon denitrification rates in sandy soils

Dentrification rates in two soils were assessed separately as a function of NO₃^? concentration while providing a constant initial glucose concentration, and as a function of glucose concentration while providing a constant initial NO₃^?-N concentration. Of the soils used, a Hanford sandy loam and a Coachella fine sand, the bacteria in the former produced higher rates of denitrification with a maximum loss of 1500 μg NO₃^?-N/ml day^?1 as compared to a loss of 150 μg NO₃^?-N/ml day^?1 from the latter. Rates of loss closely approximated Michaelis Menten kinetics in the Coachella sand, and K_m values for glucose-C and NO₃^?-N were 500 μg/ml and 170 μg/ml, respectively. Rates of loss of NO₃^?-N from the Hanford soil did not approximate Michaelis-Menten kinetics, and this was attributed to failure to saturate enzyme systems in the denitrifying bacteria with glucose and nitrogen when each was held constant. C/N ratios around 2 appeared to provide the greatest rates of denitrification. High C/N ratios or high glucose concentrations (1.8 per cent) retarded denitrification, with fungal growth and a subsequent drop in pH occuring. A Pseudomonas was incubated aerobically for 24 h followed by a 72 h anaerobic incubation with nitrate as the sole nitrogen source at 0, 10, 50, 100, 250 and 500mg N/ml concentrations. Assimilatory nitrate reduction never exceeded 75 mg N/ml, and it was concluded that this mode of nitrate reduction is insignificant at higher nitrate concentrations by comparison to dissimilatory nitrate reduction, i.e. denitrification.