Improving the Accuracy of Diffusion for Inorganic 15N Analyses of Soil Extracts and Water

Sequential diffusion techniques used to speciate inorganic nitrogen-15 (¹⁵N) during soil or water analysis are complicated by incomplete recovery of ammonium (NH₄⁺)-N, introducing error in the subsequent determination of nitrate (NO₃^–)-N. Based on studies to evaluate different strategies for minimizing cross-contamination error in Mason-jar diffusions, a simple cleaning technique was developed that involves an additional 6-h diffusion using 0.6 M boric acid (H₃BO₃) at room temperature following the recovery of NH₄⁺-N. This technique was 60–87% effective for reducing cross-contamination of unlabeled NO₃^–-N by labeled NH₄⁺-N and became more effective for controlling analytical error with decreasing sample volumes, lower NH₄⁺-N enrichment, and larger quantities of NO₃^–-N. When used with the cleaning technique described, sequential diffusions were far superior for ¹⁵N analysis of NO₃^–-N, as compared to the nonsequential approach that involves an isotope dilution calculation after separate diffusions to determine NH₄⁺-N and total mineral N.     

Comparison of Factors Affecting Soil Nitrate Nitrogen and Ammonium Nitrogen Extraction

Extraction of soil nitrate nitrogen (NO₃ ^?-N) and ammonium nitrogen (NH₄ ⁺-N) by chemical reagents and their determinations by continuous flow analysis were used to ascertain factors affecting analysis of soil mineral N. In this study, six factors affecting extraction of soil NO₃ ^?-N and NH₄ ⁺-N were investigated in 10 soils sampled from five arable fields in autumn and spring in northwestern China, with three replications for each soil sample. The six factors were air drying, sieve size (1, 3, and 5 mm), extracting solution [0.01 mol L^?1 calcium chloride (CaCl₂), 1 mol L^?1 potassium chloride (KCl), and 0.5 mol L^?1 potassium sulfate (K₂SO₄)] and concentration (0.5, 1, and 2 mol L^?1 KCl), solution-to-soil ratio (5:1, 10:1, and 20:1), shaking time (30, 60, and 120 min), storage time (2, 4, and 6 weeks), and storage temperature (?18 ^oC, 4 ^oC, and 25 ^oC) of extracted solution. The recovery of soil NO₃ ^?-N and NH₄ ⁺-N was also measured to compare the differences of three extracting reagents (CaCl₂, KCl, and K₂SO₄) for NO₃ ^?-N and NH₄ ⁺-N extraction. Air drying decreased NO₃ ^?-N but increased NH₄ ⁺-N concentration in soil. Soil passed through a 3-mm sieve and shaken for 60 min yielded greater NO₃ ^?-N and NH₄ ⁺-N concentrations compared to other treatments. The concentrations of extracted NO₃ ^?-N and NH₄ ⁺-N in soil were significantly (P < 0.05) affected by extracting reagents. KCl was found to be most suitable for NO₃ ^?-N and NH₄ ⁺-N extraction, as it had better recovery for soil mineral N extraction, which averaged 113.3% for NO₃ ^?-N and 94.9% for NH₄ ⁺-N. K₂SO₄ was not found suitable for NO₃ ^?-N extraction in soil, with an average recovery as high as 137.0%, and the average recovery of CaCl₂ was only 57.3% for NH₄ ⁺-N. For KCl, the concentration of extracting solution played an important role, and 0.5 mol L^?1 KCl could fully extract NO₃ ^?-N. A ratio of 10:1 of solution to soil was adequate for NO₃ ^?-N extraction, whereas the NH₄ ⁺-N concentration was almost doubled when the solution-to-soil ratio was increased from 5:1 to 20:1. Storage of extracted solution at ?18 °C, 4 °C, and 25 °C had no significant effect (P < 0.05) on NO₃ ^?-N concentration, whereas the NH₄ ⁺-N concentration varied greatly with storage temperature. Storing the extracted solution at ?18 ^oC obtained significantly (P < 0.05) similar results with that determined immediately for both NO₃ ^?-N and NH₄ ⁺-N concentrations. Compared with the immediate extraction, the averaged NO₃ ^?-N concentration significantly (P < 0.05) increased after storing 2, 4, and 6 weeks, respectively, whereas NH₄ ⁺-N varied in the two seasons. In conclusion, using fresh soil passed through a 3-mm sieve and extracted by 0.5 mol L^?1 KCl at a solution-to-soil ratio of 10:1 was suitable for extracting NO₃ ^?-N, whereas the concentration of extracted NH₄ ⁺-N varied with KCl concentration and increased with increasing solution-to-soil ratio. The findings also suggest that shaking for 60 min and immediate determination or storage of soil extract at ?18 ^oC could improve the reliability of NO₃ ^?-N and NH₄ ⁺-N results.     

Inorganic N analysis of soil extracts by automated and distillation procedures

Abstract

A comparison was made of automated procedures and steam distillation for analysis of NH₄ ⁺ and NO₃ ^‐ in KCl extracts of soils. Automated analysis of NH₄ ⁺ utilized the phenate‐hypochlorite reaction. Nitrate was analyzed by E. coli reduction of NO₃ ^‐ to NO₂‐which was then determined colorimetrically by reaction with sulfanilamide and napthylethylenediamine diHCl. Soil extracts were made with 1 M and 2 M KCl. Extracting with 1 M KCl was as effective as 2 M KCl. Extracts in 1 M KCl did not interfere with E. coli reduction of NO₃‐, but 2 M KCl did. The automated procedures when compared to distillation gave similar if not better precision and reduced variation particularly at low N concentrations. The automated procedure tended to give higher values at higher NO₃‐concentrations. Reduced time required for the analyses provided an additional advantage for the automated procedures.     

Quantification of nitrogen excretion rates for three lumbricid earthworms using 15N

 Nitrogen excretion rates of ¹⁵N-labeled earthworms and contributions of ¹⁵N excretion products to organic (dissolved organic N) and inorganic (NH₄-N, NO₃-N) soil N pools were determined at 10  °C and 18  °C under laboratory conditions. Juvenile and adult Lumbricus terrestris L., pre-clitellate and adult Aporrectodea tuberculata (Eisen), and adult Lumbricus rubellus (Hoffmeister) were labeled with ¹⁵N by providing earthworms with ¹⁵N-labeled organic substrates for 5–6 weeks. The quantity of ¹⁵N excreted in unlabeled soil was measured after 48 h, and daily N excretion rates were calculated. N excretion rates ranged from 274.4 to 744 μg N g^–1 earthworm fresh weight day^–1, with a daily turnover of 0.3–0.9% of earthworm tissue N. The N excretion rates of juvenile L. terrestris were significantly lower than adult L. terrestris, and there was no difference in the N excretion rates of pre-clitellate and adult A. tuberculata. Extractable N pools, particularly NH₄-N, were greater in soils incubated with earthworms for 48 h than soils incubated without earthworms. Between 13 and 40% of excreted ¹⁵N was found in the ¹⁵N-mineral N (NH₄-N+NO₃-N) pool, and 13–23% was in the ¹⁵N-DON pool. Other fates of excreted ¹⁵N may have been incorporation in microbial biomass, chemical or physical protection in non-extractable N forms, or gaseous N losses. Earthworm excretion rates were combined with earthworm biomass measurements to estimate N flux from earthworm populations through excretion. Annual earthworm excretion was estimated at 41.5 kg N ha^–1 in an inorganically-fertilized corn agroecosystem, and was equivalent to 22% of crop N uptake. Our results suggest that the earthworms could contribute significantly to N cycling in corn agroecosystems through excretion processes. Received: 12 April 1999     

Evaluation of 3,4-dimethylpyrazole phosphate as a nitrification inhibitor in a <Emphasis Type="Italic">Citrus</Emphasis>-cultivated soil

 The objectives of this work were to evaluate the inhibitory action on nitrification of 3,4-dimethylpyrazole phosphate (DMPP) added to ammonium sulphate nitrate [(NH₄)₂SO₄ plus NH₄NO₃; ASN] in a Citrus-cultivated soil, and to study its effect on N uptake. In a greenhouse experiment, 2 g N as ASN either with or without 0.015 g DMPP (1% DMPP relative to NH₄ ⁺-N) was applied 6 times at 20-day intervals to plants grown in 14-l pots filled with soil. Addition of DMPP to ASN resulted in higher levels of NH₄ ⁺-N and lower levels of NO₃ ^–-N in the soil during the whole experimental period. The NO₃ ^–-N concentration in drainage water was lower in the ASN plus DMPP (ASN+DMPP)-treated pots. Also, DMPP supplementation resulted in greater uptake of the fertilizer-N by citrus plants. In another experiment, 100 g N as ASN, either with or without 0.75 g DMPP (1% DMPP relative to NH₄ ⁺-N) was applied to 6-year-old citrus plants grown individually outdoors in containers. Concentrations of NH₄ ⁺-N and NO₃ ^–-N at different soil depths and N distribution in the soil profile after consecutive flood irrigations were monitored. In the ASN-amended soil, nitrification was faster, whereas the addition of the inhibitor led to the maintenance of relatively high levels of NH₄ ⁺-N and NO₃ ^–-N in soil for longer than when ASN was added alone. At the end of the experiment (120 days) 68.5% and 53.1% of the applied N was leached below 0.60 m in the ASN and ASN+DMPP treatments, respectively. Also, leaf N levels were higher in plants fertilized with ASN+DMPP. Collectively, these results indicate that the DMPP nitrification inhibitor improved N fertilizer efficiency and reduced NO₃ ^– leaching losses by retaining the applied N in the ammoniacal form. Received: 31 May 1999     

Utilization of waste office paper to reduce nitrate leaching into the Northern Guam aquifer

 Rapid nitrate leaching losses due to current agricultural N management practices under the humid tropical environmental conditions of the Pacific island of Guam may contaminate fresh and salt water resources. Potential environmental contamination of the Northern Guam aquifer, which is overlain by shallow limestone-derived soils, is a major public concern because the aquifer is the sole underground source of fresh water for the island. The objectives of this study were to examine the use of waste office paper as a possible management alternative for reducing nitrate leaching due to N fertilizer applications in northern Guam while also providing sufficient N for crop growth. In a laboratory study, increasing rates of waste paper application reduced NO₃ ^–-N leaching up to approximately 200 days after incorporation of N fertilizer and paper treatments. Subsequent mineralization of immobilized N from paper applications was also observed, although cumulative NO₃ ^–-N leaching at the highest rate of paper addition was lower than the control after 394 days of incubation. The effect of waste paper on N availability and NO₃ ^–-N leaching after application of N fertilizer at rates up to 500 kg N ha^–1 was also evaluated in two field experiments planted with sweet corn (Zea mays var. rugosa Bonaf.) during consecutive dry and wet periods. Leaching losses of NO₃ ^–-N were higher during the wet cropping season, leading to lower crop yields and crop N uptake. Combining paper with N fertilizer reduced NO₃ ^–-N leaching losses but also decreased crop ear yields up to N fertilizer application rates of 250 kg N ha^–1 during the dry cropping season and up to rates of 100 kg N ha^–1 during the wet period. Although combining waste paper with N fertilizer reduced NO₃ ^–-N leaching losses, no improvements in fertilizer N recovery were observed during the field experiments. This lack of crop response may be due to the importance of early season N availability for the short-season horticultural crops grown on Guam. We suggest that the application of waste paper may be a useful management practice to reduce NO₃ ^–-N leaching losses when high soil NO₃ ^–-N levels remain after cropping due either to crop failure or to over-application of N fertilizer. Received: 11 May 1999     

Influence of N and non-N salts on atmospheric methane oxidation by upland boreal forest and tundra soils

 The short-term (24 h) and medium-term (30 day) influence of N salts (NH₄Cl, NaNO₃ and NaNO₂) and a non-N salt (NaCl) on first-order rate constants, k (h^–1) and thresholds (C_Th) for atmospheric CH₄ oxidation by homogenized composites of upland boreal forest and tundra soils was assessed at salt additions ranging to 20 μmol g^–1 dry weight (dw) soil. Additions of NH₄Cl, NaNO₃ and NaCl to 0.5 μmol g^–1 dw soil did not significantly decrease k relative to watered controls in the short term. Higher concentrations significantly reduced k, with the degree of inhibition increasing with increasing dose. Similar doses of NH₄Cl and NaCl gave comparable decreases in k relative to controls and both soils showed low native concentrations of NH₄ ⁺-N (≤1 μmol g^–1dw soil), suggesting that the reduction in k was due primarily to a salt influence rather than competitive inhibition of CH₄ oxidation by exogenous NH₄ ⁺-N or NH₄ ⁺-N released through cation exchange. The decrease in k was consistently less for NaNO₃ than for NH₄Cl and NaCl at similar doses, pointing to a strong inhibitory effect of the Cl^– counter-anion. Thresholds for CH₄ oxidation were less sensitive to salt addition than k for these three salts, as significant increases in C_Th relative to controls were only observed at concentrations ≥1.0 μmol g^–1 dw soil. Both soils were more sensitive to NaNO₂ than to other salts in the short term, showing a significant decrease in k at an addition of 0.25 μmol NaNO₂ g^–1 dw soil that was clearly attributable to NO₂ ^–. Soils showed no recovery from NaCl, NH₄ ⁺-N or NaNO₃ addition with respect to atmospheric CH₄ oxidation after 30 days. However, soils amended with NaNO₂ to 1.0 μmol NaNO₂ g^–1 dw showed values of k that were not significantly different from controls. Recovery of CH₄-oxidizing ability was due to complete oxidation of NO₂ ^–-N to NO₃ ^–-N. Analysis of soil concentrations of N salts necessary to inhibit atmospheric CH₄ oxidation and regional rates of N deposition suggest that N deposition will not decrease the future sink strength of upland high-latitude soils in the atmospheric CH₄ budget. Received: 30 April 1999     

Recovery of fertilizer nitrogen from continuous corn soils under contrasting tillage management

Tillage systems influence soil properties and may influence the availability of applied and mineralized soil N. This laboratory study (20°C) compared N cycling in two soils, a Wooster (fine, loamy Typic Fragiudalf) and a Hoytville (fine, illitic Mollic Epiaqualf) under continuous corn (Zea mays) production since at least 1963 with no-tillage (NT), minimum (CT) and plow tillage (PT) management. Fertilizer was added at the rate of 100 mg ¹⁵N kg^–1–1 soil as 99.9% ¹⁵N as NH₄Cl or Ca(NO₃)₂ and the soils were incubated in leaching columns for 1 week at 34 kPa before being leached periodically with 0.05 M CaCl₂ for 26 weeks. As expected, the majority of the ¹⁵NO₃^– additions were removed from both soils with the first leaching. The majority of applied ¹⁵NH₄⁺ additions were recovered as ¹⁵NO₃^– by week 5, with the NT soils demonstrating faster nitrification rates compared with soils under other tillage practices. For the remaining 22 weeks, only low levels of ¹⁵NO₃^– were leached from the soils regardless of tillage management. In the coarser textured Wooster soils (150 g clay kg^–1), mineralization of native soil N in the fertilized soils was related to the total N content (r² 0.99) and amino acid N (r² 0.99), but N mineralization in the finer textured Hoytville (400 g clay kg^–1) was constant across tillage treatments and not significantly related to soil total N or amino acid N content. The release of native soil N was enhanced by NH₄⁺ or NO₃^– addition compared to the values released by the unfertilized control and exceeded possible pool substitution. The results question the use of incubation N mineralization tests conducted with unfertilized soils as a means for predicting soil N availability for crop N needs.     

Evaluation of biological and chemical nitrogen indices for predicting nitrogen-supplying capacity of paddy soils in the Taihu Lake region,China

Simple and rapid chemical indices of soil nitrogen (N)-supplying capacity are necessary for fertilizer recommendations. In this study, pot experiment involving rice, anaerobic incubation, and chemical analysis were conducted for paddy soils collected from nine locations in the Taihu Lake region of China. The paddy soils showed large variability in N-supplying capacity as indicated by the total N uptake (TNU) by rice plants in a pot experiment, which ranged from 639.7 to 1,046.2 mg N pot⁻¹ at maturity stage, representing 5.8% of the total soil N on average. Anaerobic incubation for 3, 14, 28, and 112 days all resulted in a significant (P < 0.01) correlation between cumulative mineral NH₄⁺-N and TNU, but generally better correlations were obtained with increasing incubation time. Soil organic C, total soil N, microbial C, and ultraviolet absorbance of NaHCO₃ extract at 205 and 260 nm revealed no clear relationship with TNU or cumulative mineral NH₄⁺-N. Soil C/N ratio, acid KMnO₄-NH₄⁺-N, alkaline KMnO₄-NH₄⁺-N, phosphate–borate buffer extractable NH₄⁺-N (PB-NH₄⁺-N), phosphate–borate buffer hydrolyzable NH₄⁺-N (PB_HYDR-NH₄⁺-N) and hot KCl extractable NH₄⁺-N (H_KCl−NH₄⁺-N) were all significantly (P < 0.05) related to TNU and cumulative mineral NH₄⁺-N of long-term incubation (>28 days). However, the best chemical index of soil N-supplying capacity was the soil C/N ratio, which showed the highest correlation with TNU at maturity stage (R = −0.929, P < 0.001) and cumulative mineral NH₄⁺-N (R = −0.971, P < 0.001). Acid KMnO₄-NH₄⁺-N plus native soil NH₄⁺-N produced similar, but slightly worse predictions of soil N-supplying capacity than the soil C/N ratio.     

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.     

Nitrogen fertilizers promote denitrification

A laboratory study was conducted to compare the effects of different N fertilizers on emission of N₂ and N₂O during denitrification of NO₃ ^– in waterlogged soil. Field-moist samples of Drummer silty clay loam soil (fine-silty, mixed, mesic Typic Haplaquoll) were incubated under aerobic conditions for 0, 2, 4, 7, 14, 21, or 42 days with or without addition of unlabelled (NH₄)₂SO₄, urea, NH₄H₂PO₄, (NH₄)₂HPO₄, NH₄NO₃ (200 or 1000 mg N kg^–1 soil), or liquid anhydrous NH₃ (1000 mg N kg^–1 soil). The incubated soil samples were then treated with ¹⁵N-labelled KNO₃ (250 mg N kg^–1 soil, 73.7 atom% ¹⁵N), and incubation was carried out under waterlogged conditions for 5 days, followed by collection of atmospheric samples for ¹⁵N analyses to determine labelled N₂ and N₂O. Compared to samples incubated without addition of unlabelled N, all of the fertilizers promoted denitrification of ¹⁵NO₃ ^–. Emission of labelled N₂ and N₂O decreased in the order: Anhydrous NH₃>urea<$>\gg<$> (NH₄)₂HPO₄>(NH₄)₂SO₄≃NH₄NO₃≃NH₄H₂PO₄. The highest emissions observed with anhydrous NH₃ or urea coincided with the presence of NO₂ ^–, and ¹⁵N analyses indicated that these emissions originated from NO₂ ^– rather than NO₃ ^–. Emissions of labelled N₂ and N₂O were significantly correlated with fertilizer effects on soil pH and water-soluble organic C. Received: 17 January 1996     

Exchangeable ammonium and nitrate from different nitrogen fertilizer preparations in polyacrylamide-treated and untreated agricultural soils

 High molecular weight, anionic polyacrylamide (PAM) is currently being used as an irrigation water additive to significantly reduce soil erosion associated with furrow irrigation. PAM contains amide-N, and PAM application to soils has been correlated with increased activity of soil enzymes, such as urease and amidase, involved in N cycling. Therefore we investigated potential impacts of PAM treatment on the rate at which fertilizer N is transformed into NH₄ ⁺ and NO₃ ^– in soil. PAM-treated and untreated soil microcosms were amended with a variety of fertilizers, ranging from common rapid-release forms, such as ammonium sulfate [(NH₄)₂SO₄] and urea, to a variety of slow-release formulations, including polymerized urea and polymer-encapsulated urea. Ammonium sulfate was also tested together with the nitrification inhibitor dicyandiamide (DCD). The fertilizers were applied at a concentration of 1.0 mg g^–1, which is comparable to 100 lb acre^–l, or 112 kg ha^–1. Potassium chloride-extractable NH₄ ⁺-N and NO₃ ^–-N were quantified periodically during 2–4 week incubations. PAM treatment had no significant effect on NH₄ ⁺ release rates for any of the fertilizers tested and did not alter the efficacy of DCD as a nitrification inhibitor. However, the nitrification rate of urea and encapsulated urea-derived NH₄ ⁺-N was slightly accelerated in the PAM-treated soil. Received: 16 January 1998     

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⁺.     

A Comparison of Diffusion-Conductimetric and Distillation-Titration Methods in Analyzing Ammonium- and Nitrate-Nitrogen in the KCl-Extracts of Georgia Soils

Soil mineral (or inorganic) nitrogen (SMN), which primarily exists as exchangeable and soluble ammonium (NH4⁺) and the nitrate (NO₃^?) ions, represents readily available nitrogen for plant growth. Over the years a 2M potassium chloride (KCl) solution has become the extraction solution of choice for extracting SMN. In the research and service laboratories, either distillation-titration method (DTM) or colorimetric method (CM) is virtually the standard to measure NH₄⁺- and NO₃^?-N in the 2M KCl soil extracts. However, being a time-consuming and labor intensive method, DTM generally has a very low throughput. Likewise, CM is affected by interferences from pH variation, color, turbidity, presence of organic species, and some other constituents in the extracts. In contrast, diffusion conductivity method (DCM) is a less expensive and high throughput one, which is also relatively free from common interferences. In this study, we, therefore, compared the extraction efficiency of various KCl concentrations and performance of diffusion conductivity method (DCM) with DTM in measuring NH₄⁺-N and NO₃^?-N in KCl extracts of 32 agricultural soils of Georgia. A 0.2M KCl solution extracted statistically similar amounts of NH₄⁺-N and NO₃^?-N as did 2M KCl, suggesting that a 10-fold dilute KCl solution than the standard 2M KCl might be good enough to extract and estimate the most of SMN. For the analyses of NH₄⁺- and NO₃^?-N in the KCl extracts, the DCM produced results statistically similar to those produced by DTM. The deviation between the results given by DCM and DTM was no more than ±10%. Thus, DCM appears to be an attractive alternative to the labor intensive and time-consuming DTM for measuring NH₄⁺- and NO₃^?-N in the KCl extract of soils in the research and service laboratories.     

Extraction of nitrogen from soils

Summary A roller bed and rotary end-over-end shaker were compared for the extraction of mineral N from a variety of soil types; both were equally efficient with an optimum extraction time of 30 min. However, the roller bed permitted a greater operational capacity, a faster throughput of samples, and easier identification of sample bottles compared with the end-over-end shaker. More NH₄ ⁺-N and NO₃ ^–-N (P<0.001) was recovered from soil by 2 M KCl than by any other extractant, in a soil: extractant ratio of 1 to 5 (w:v), except water, which was equally efficient at removing NO₃ ^–-N from soils.     

Emissions of nitrous oxide from a constructed wetland using a groundfilter and macrophytes in waste-water purification of a dairy farm

 In less populated rural areas constructed wetlands with a groundfilter made out of the local soil mixed with peat and planted with common reed (Phragmites australis) are increasingly used to purify waste water. Particularly in the rhizosphere of the reed, nitrification and denitrification processes take place varying locally and temporally, and the question arises to what extent this type of waste-water treatment plant may contribute to the release of N₂O. In situ N₂O measurements were carried out in the two reed beds of the Friedelhausen dairy farm, Hesse, Germany, irrigated with the waste water from a cheese dairy and 70 local inhabitants (12 m³ waste water or 6 kg BOD₅ or 11 kg chemical O₂ demand (COD_Mn) day^–1). During November 1995 to March 1996, the release of N₂O was measured weekly at 1 m distances using eight open chambers and molecular-sieve traps to collect and absorb the emitted N₂O. Simultanously, the N₂O trapped in the soil, the soil temperature, as well as the concentrations of NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, water-soluble C and the pH were determined at depths of 0–20, 20–40 and 40–60 cm. In the waste water from the in- and outflow the concentrations of COD_Mn, BOD₅, NH₄ ⁺-N, NO₃ ^–-N, NO₂ ^–-N, as well as the pH, were determined weekly. Highly varying amounts of N₂O were emitted at all measuring dates during the winter. Even at soil temperatures of –1.5  °C in 10 cm depth of soil or 2  °C at a depth of 50 cm, N₂O was released. The highest organic matter and N transformation rates were recorded in the upper 20 cm of soil and in the region closest to the outflow of the constructed wetland. Not until a freezing period of several weeks did the N₂O emissions drop drastically. During the period of decreasing temperatures less NO₃ ^–-N was formed in the soil, but the NH₄ ⁺-N concentrations increased. On average the constructed wetlands of Friedelhausen emitted about 15 mg N₂O-N inhabitant equivalent^–1 day^–1 during the winter period. Nitrification-denitrification processes rather than heterotrophic denitrification are assumed to be responsible for the N₂O production. Received: 28 October 1998     

Effects of salts and moisture content on N2O emission and nitrogen dynamics in Yellow soil and Andosol in model experiments

 The effects of salt type and its concentration on nitrification, N mineralization and N₂O emission were examined under two levels of moisture content in Yellow soil and Andosol samples as simulated to agriculture under arid/semi-arid conditions and under heavy application of fertilizer in a glass-house, respectively. The salt mixtures were composed of chlorides (NaCl and NH₄Cl) or sulphates [Na₂SO₄ and (NH₄)₂SO₄] and were added at various concentrations (0, 0.1, 0.2, 0.4 and 0.6 M as in the soil solution). These salts were added to non-saline Yellow soil at different moisture contents (45 or 40 and 65% of maximum water-holding capacity; WHC) and their effects on the changes in mineral N (NH₄ ⁺-N and NO₃ ^–-N) concentration as well as N₂O emission were examined periodically during laboratory incubation. We also measured urease activities to know the effect of salts on N mineralization. Furthermore, Ca(NO₃)₂ solution was added at various concentrations (0, 0.1, 0.3, 0.5 and 0.8 M as in the soil solution) to a non-saline Andosol taken from the subsurface layer in a glass-house and incubated at different moisture contents (50% and 70% of WHC) to examine their effects on changes in mineral N. Nitrification was inhibited by high, but remained unaffected by low, salt concentrations. These phenomena were shown in both the model experiments. It was considered that the salinity level for inhibition of nitrification was an electric conductivity (1 : 5) of 1 dS m^–1. This level was independent of the type of salts or soil, and was not affected by soil moisture content. The critical level of salts for urease activities was about 2 dS m^–1. The emission rate of N₂O was maximum at the beginning of the incubation period and stabilized at a low level after an initial peak. There was no significant difference in N₂O emission among the treatments at different salt concentrations, while higher moisture level enhanced N₂O emission remarkably. Received: 29 July 1998     

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.     

Land use affects the distribution of soil inorganic nitrogen in smallholder production systems in Kenya

 We hypothesized that the integration of trees and shrubs in agricultural landscapes can reduce NO₃ ^– leaching and increase utilization of subsoil N. A field survey was conducted on 14 farms on acid soils in the subhumid highlands of Kenya, where there is little use of fertilizers, to determine the effect of vegetation types (VT) on soil NH₄ ⁺ and NO₃ ^– to 4 m depth. The VT included maize (Zea mays) with poor growth and good growth, Markhamia lutea trees scattered in maize, natural weed fallow, banana (Musa spp.), hedgerow, and eucalyptus woodlot. The effect of VT on NH₄ ⁺ was small (<1 mg N kg^–1). NO₃ ^– within a VT was about constant with depth below 0.25 m, but subsoil NO₃ ^– varied greatly among VT. Mean NO₃ ^–-N concentrations at 0.5–4 m depth were low beneath hedgerow and woodlot (<0.2 mg kg^–1), intermediate beneath weed fallow (0.2–0.7 mg kg^–1), banana (0.5–1.0 mg kg^–1) and markhamia (0.5–1.6 mg kg^–1), and high beneath both poor (1.0–2.1 mg kg^–1) and good (1.9–3.1 mg kg^–1) maize. Subsoil NO₃ ^– (0.5–4 m) was agronomically significant after maize harvest with 37 kg N ha^–1 m^–1 depth of subsoil beneath good maize and 27 kg N ha^–1 m^–1 depth beneath poor maize. In contrast, subsoil NO₃ ^– was only 2 kg N ha^–1 m^–1 depth beneath woodlot and hedgerow. These results demonstrate that the integration of perennial vegetation and the rotation of annual and perennial crops can tighten N cycling in agricultural landscapes. Received: 8 July 1999     

Uptake,transport and assimilation of 15N-nitrate and 15N-ammonium in tea (Camellia sinensis L.) plants

¹⁵N studies were conducted using hydroponically grown tea (Camellia sinensis L.) plants to clarify the characteristics of uptake, transport and assimilation of nitrate and ammonium. From the culture solution containing 50 mg L^-1 N0₃-N and 50 mg L^-1 NH.-N, the uptake of NH₃-N after 24 h was twice as high as that of NO₃-N, while the uptake of N0₃-N from the culture solution containing 90 mg N0₃-N and 10 mg NH₃-N was twice that of NH₄-N. The presence of 0.4 mM Al had no significant effect on the N0₃-N and NH₄-N uptake from the culture solutions containing 50 mg L^-1 N0₃-N and 50 mg L^-1 NH₄-N, 90 mg L^-1 N0₃-N and 10 mg L^-1 NH₄-N or 99 mg L^-1 N0₃-N and 1 mg L^-1 NH₄-N. Transport of N0₃-derived N to young leaves was much more rapid than that of NH₄-derived NO₃ and NH₄-derived N was largely retained in the roots and lower stem. Young and mature shoots separated from the roots absorbed more N0₃-N than intact plants. Nitrate assimilation occurred in both, roots and young as well as mature leaves. Internal cycling of N0₃-derived Nand NH₄-derived N from one root part to another part was not appreciable after 28 h, suggesting that a longer of time is required for cycling in woody plants.