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

Abstract

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

Extraction of soil nitrogen by chloroform fumigation – A new index for the evaluation of soil nitrogen supply

The N extracted after chloroform (CHCl₃) fumigation was determined as a possible index of soil N supply to plants. The relationships between extractable N following fumigation and reference indices such as total N, alkali-hydrolyzable N, N released by the Stanford short-term incubation method, and the N extracted by KCl and by CaCl₂, were measured in nine soils of differing soil N supply capacity. A highly significant correlation was achieved between the extractable N released by fumigation and the N released by the Stanford method, i.e. a short-term aerobic incubation (r = 0.87). Similarly, the correlation between extractable N by fumigation and the N uptake by ryegrass was highly statistically significant (r = 0.93). Using the N extracted following fumigation has the advantage that laboratory results are available in two days and are both reproducible and of high precision. Therefore, the N extracted following fumigation is a valid, timesaving and precise index of soil N supply capacity.     

Evaluation of nitrogen availability in a soil treated with organic amendments

Abstract

In the search for an approach which could be used to predict available nitrogen (N) in organic amendments, biological and chemical methods were investigated in laboratory and growth chamber studies. Two biological methods [maize plants (Zea mays L.) grown in pots, and soil‐amendment mixtures incubated aerobically at 2, 4, 6, 8, 12, and 16 weeks], and four chemical methods [autoclave, 0.5M potassium permanganate (KMnO₄), pepsin, and 6M hydrochloric acid (HCl)] were compared to determine N availability in 36 organic amendments applied to soil. Total N mineralized in a soil amended with different organic amendments ranged from‐12 to 428 mg N/kg soil. The highest value was obtained from sludge number 11 and the lowest from cow manure 2, urban refuse, and grape‐marc. In general, the aerobically‐treated sewage sludges gave higher N‐mineralization rates than other amendments. The 6M HCl and autoclave methods were more suitable for predicting N availability in these organic amendments than either the pepsin or KMnO₄ methods. Prediction of N availability in the growth chamber experiments improved if several chemical and biological methods were combined in a multiple regression analysis.     

Arylamidase Activity as an Index of Nitrogen Mineralization in Soils

Abstract

The enzyme arylamidase [EC 3.4.11.2] catalyzes the hydrolysis of N‐terminal amino acids from arylamides. Because it has been proposed that this enzyme may play a major role in nitrogen (N) mineralization in soils, studies were carried out using short‐term laboratory incubations under aerobic and anaerobic conditions and chemical hydrolysis of soil organic N to assess the N mineralization in a range of 51 soils from six agroecological zones of the North Central region of the United States. The enzyme activity was assayed at its optimal pH value. With the exception of the values obtained for field‐moist soils incubated under anaerobic conditions, the amounts of N mineralized by all the biological and chemical methods studied were significantly correlated with arylamidase activity, with r values of 0.54*** for the amounts of inorganic N produced under aerobic incubation, of 0.44** for anaerobic incubation of air‐dried soils, of 0.53*** and 0.55*** for the amounts of ammonium (NH₄ ⁺)‐N released by steam distillation with PO₄‐B₄O₇ for 4 and 8 min, respectively; and of 0.49*** and 0.53*** for the amounts of NH₄ ⁺‐N released by steam distillation with disodium tetraborate (Na₂B₄O₇) for 4 min or 8 min, respectively. The amounts of N extractable with hot potassium chloride (KCl) were most significantly correlated with arylamidase activity (r=0.56***). Arylamidase activity was significantly correlated with organic carbon (C) (r=0.49***), organic N (r=0.55***), and fixed ammonium (NH₄ ⁺)‐N (r =0.42**).     

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.     

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

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

Comparison of chemical methods of assessing potentially available organic nitrogen in soil

Abstract

We recently developed two rapid and precise chemical methods of assessing potentially available organic N in soils. One method involves determination of the ammonia‐N produced by steam distillation of the soil sample with pH 11.2 phosphate‐borate buffer solution for 8 min. The other involves determination of the ammonium‐N produced by treatment of the soil sample with 2M KCl solution at 100°C for 4 hours. Studies using 33 Brazilian soils showed that the results obtained by these methods were highly correlated with those obtained by anaerobic and aerobic incubation methods of assessing potentially available organic N in soil.

The two methods were further evaluated by applying them to 30 Iowa soils and by comparing their results and those obtained by other chemical methods with the results of the incubation methods considered to be the best laboratory methods currently available for assessment of potentially available organic N in soil. The chemical methods used included the acid KMnO₄ method, the alkaline KMnO₄ method, the CaCl₂‐autoclave method, and the NaHCO₃ UV method. The incubation methods used involved determination of the ammonium‐N produced by incubation of the soil sample under anaerobic conditions for 1 week or determination of the (ammonium + nitrate + nitrite)‐N produced by incubation of the sample under aerobic conditions for 2 and 12 weeks. The data obtained showed that the results of the two chemical methods evaluated were highly correlated with those obtained by the incubation techniques used for comparison and that the correlations observed with these two methods were higher than those observed with the previously proposed chemical methods. It is concluded that these two rapid and simple methods are the best chemical methods thus far developed for laboratory assessment of potentially available organic N in soil.     

Mobile and readily available C and N fractions and their relationship to microbial biomass and selected enzyme activities in a sandy soil under different management systems

Within different land‐use systems such as agriculture, forestry, and fallow, the different morphology and physiology of the plants, together with their specific management, lead to a system‐typical set of ecological conditions in the soil. The response of total, mobile, and easily available C and N fractions, microbial biomass, and enzyme activities involved in C and N cycling to different soil management was investigated in a sandy soil at a field study at Riesa, Northeastern Germany. The management systems included agricultural management (AM), succession fallow (SF), and forest management (FM). Samples of the mineral soil (0—5, 5—10, and 10—30 cm) were taken in spring 1999 and analyzed for their contents on organic C, total N, NH₄⁺‐N and NO₃^—‐N, KCl‐extractable organic C and N fractions (Corg_(KCl) and Norg_(KCl)), microbial biomass C and N, and activities of β‐glucosidase and L‐asparaginase. With the exception of Norg_(KCl), all investigated C and N pools showed a clear relationship to the land‐use system that was most pronounced in the 0—5 cm profile increment. SF resulted in greater contents of readily available C (Corg_(KCl)), NH₄⁺‐N, microbial biomass C and N, and enzyme activities in the uppermost 5 cm of the soil compared to all other systems studied. These differences were significant at P ≤ 0.05 to P ≤ 0.001. Comparably high C_mic:C_org ratios of 2.4 to 3.9 % in the SF plot imply a faster C and N turnover than in AM and FM plots. Forest management led to 1.5‐ to 2‐fold larger organic C contents compared to SF and AM plots, respectively. High organic C contents were coupled with low microbial biomass C (78 μg g^—1) and N contents (10.7 μg g^—1), extremely low C_mic : C_org ratios (0.2—0.6 %) and low β‐glucosidase (81 μg PN g^—1 h^—1) and L‐asparaginase (7.3 μg NH₄‐N g^—1 2 h^—1) activities. These results indicate a severe inhibition of mineralization processes in soils under locust stands. Under agricultural management, chemical and biological parameters expressed medium values with exception for NO₃^—‐N contents which were significantly higher than in SF and FM plots (P ≤ 0.005) and increased with increasing soil depth. Nevertheless, the depth gradient found for all studied parameters was most pronounced in soils under SF. Microbial biomass C and N were correlated to β‐glucosidase and L‐asparaginase activity (r ≥ 0.63; P ≤ 0.001). Furthermore, microbial biomass and enzyme activities were related to the amounts of readily mineralizable organic C (i.e. Corg_(KCl)) with r ≥ 0.41 (P ≤ 0.01), suggesting that (1) KCl‐extractable organic C compounds from field‐fresh prepared soils represent an important C source for soil microbial populations, and (2) that microbial biomass is an important source for enzymes in soil. The Norg_(KCl) pool is not necessarily related to the size of microbial biomass C and N and enzyme activities in soil.<?show $6#>     

Comparison of two chemical methods for extracting residual N fertilizer

Summary Considerable effort has been spent in developing chemical indices to predict N mineralization. However, in spite of numerous studies, the relationship between the index value and plant N uptake has not been as apparent as hoped, and therefore, additional work is required to evaluate the ability of promising new indices to predict the extraction of mineralizable N from soil. The objective of the present study was to evaluate the use of phosphate borate and hot KCl to extract immobilized ¹⁵N-labeled fertilizer, applied 1 and 2 years previously. Soil samples (0–15 cm) were collected on 12 June 1989 from field soil fertilized in either 1987 or 1988 with ¹⁵N-labeled urea. In the laboratory, net N mineralization over 51 days and the amount of N extracted by the phosphate borate and hot KCl methods were determined. In the field, the amount of residual fertilizer and soil plus fixed N in soybeans (Glycine max) at the V5 growth stage were determined on 12 June 1989. The extractability ratio (ER^*) and the mineralizable extractability ratio (MER) were higher for mineralizable N and phosphate borate N for fertilizer applied in 1988 than 1987, while ER^* and MER values for the hot KCl were similar for both application dates. These results suggest that compositional changes occurred which influenced the extractability and mineralization of residual fertilizer applied 1 and 2 years previously, and that the phosphate borate was able to predict these changes while the hot KCl method was not.     

A comparison of different indices for nitrogen mineralization

Indices of N mineralization in soils of contrasting texture, pH, and organic matter contents were compared at different dates during the growing season. The indices were derived from a 12-week aerobic incubation, determination of the amount of microbial biomass at the start of the incubation, determination of the increase in NH ₄ ⁺ after boiling with 2 M KCl for 2h, and extraction of total soluble N with 0.01 M CaCl₂. Cumulative mineral N increased linearly with time in the course of the incubations. Rates of mineralization in soil samples taken in March 1989 and 1990 were significantly correlated with soluble organic N, while correlations between the mineralization rate and the increase in NH ₄ ⁺ after boiling with 2 M KCl for 2 h were poor for sandy soils and absent for loamy soils. Correlations between NH ₄ ⁺ after boiling with 2 M KCl for 2h and the soil N concentration were highly significant, but no general relationship was found between the mineralization rate and the soil N concentration. Neither biomass N nor biomass C was significantly correlated with the mineralization rate or with one of the chemical indices. Among the methods tested, soluble organic N extracted with 0.01 M CaCl₂ was the only method with any promise for routine measurement of the mineralization capacity of the individual sites.     

Potential methods for estimating nitrogen fertilizer value of organic residues

New organic fertilizers based on waste products are continually being introduced in agriculture. Their nitrogen (N) fertilizer value of their total N and mineral N content varies widely, creating a demand for standardized laboratory methods. This study evaluated some potential methods for estimating the N fertilizer value of different kinds of organic fertilizers. The methods were evaluated against the N fertilizer value obtained from a ryegrass pot experiment. Fifteen fertilizers were tested, including different kinds of manure, powders from meat, bone, blood and feathers, rapeseed cake, lucerne pellets, sewage sludge, biogas residue, vinasse and mussel compost. Mineral fertilizer equivalents (MFE) were calculated as the fraction of total N (MFE) or organic N (MFE_org) out of total N that has the same availability to plants as inorganic N. Mineral N content (% of total N added with organic residue) after 4 weeks of incubation of soil was correlated to MFE (r² = 0.78), but was on average 17% lower. Warm water‐extractable N, amino acid N and crude fibre analysis all proved to be unsatisfactory as methods for estimating MFE or MFE_org. However, the carbon/nitrogen ratio accurately reflected short‐term plant‐available N through a negative linear relationship (r² = 0.83) and would thus be a very useful method for estimating MFE, with MFE decreasing by 5% per unit increase in C/N ratio. The results also indicated that the analysis of near infrared reflectance (NIR) spectra can be an even quicker and cheaper method to estimate MFE of organic residues, but this issue requires further research.     

Alkaline Hydrolyzable Organic Nitrogen as an Index of Nitrogen Mineralization in Soils: Relationship with Activities of Arylamidase and Amidohydrolases

ABSTRACT

This study investigated the relationship between a recently proposed alkaline hydrolysis method for estimating the chemical index of nitrogen (N) mineralization potential of soils and the activities of arylamidase and four amidohydrolases involved in hydrolysis of organic N (ON) in soils. Nitrogen mineralization was studied in 13 soils from uncultivated fields in Iowa, USA, by direct steam distillation of 1 g field-most soil treated with 1 M KOH or 1 M NaOH. The distillate was collected in boric acids, which was changed every 5 min for a total of 40 min. The NH₄ ⁺-N in the distillate was determined by titration with 0.005 M H₂SO₄. The cumulative amounts of N hydrolyzed were fitted to the first-order exponential equation to determine the “potentially hydrolyzable N (N_max )” for the soils. The activities of arylamidase, L-asparaginase, L-glutaminase, amidase, and L-aspartase were assayed at their optimal pH values. Results showed that estimated N_max values were strongly correlated with the activities of arylamidase and amidohydrolases. The activities of arylamidase and the amidohydrolases were significantly correlated, indicating that the activities of the two groups of enzymes are coupled in mineralization of ON in soils. Based on the specificity of enzyme reactions and the strong relationship between estimated N_max values and the activities of arylamidase and amidohydrolases, we concluded that similar amide-N bonds were susceptible to enzymatic and alkaline hydrolysis, and that alkaline hydrolyzable ON can be used as an index of N mineralization in soils.     

石灰性土壤起始NO3——N对土壤供氮能力测定方法的影响

在陕西省的澄城、永寿、杨陵 3地区选取有机质、全N、硝态N含量差异较大的 17个石灰性土壤 ,分别在淋洗与未淋洗土壤起始NO3--N后 ,利用盆栽试验探讨土壤NO3--N淋洗前、后 ,不同方法测定的已矿化N和可矿化N与小麦吸N量之间的相关性。结果表明 ,未淋洗土壤起始NO3--N ,用KCl直接浸取、KCl煮沸法所浸取以及通气培养前CaCl2 所淋洗的起始NO3--N均与小麦吸N量密切相关 ,相关系数 (r)分别为 0.934 ,0.856和 0.862 ,均达1%显著水准。与此相反 ,通气培养、淹水培养、沸水煮沸、碱性高锰酸钾、酸性高锰酸钾及碱解扩散等方法所提取的可矿化N与小麦吸N量间无显著相关。淋洗土壤起始NO3--N后 ,用KCl直接浸取、KCl煮沸法浸取以及通气培养前CaCl2 所淋洗的起始NO3--N与小麦吸N量之间的相关系数明显降低 ,达不到 5%的显著水准。而通气培养、淹水培养、沸水煮沸、碱性高锰酸钾、酸性高锰酸钾及碱解扩散等方法所提取的可矿化N与小麦吸N量之间相关系数却明显提高 ,都达到 5%或 1%的显著水平。其中变化最明显的是淹水培养 1周矿化出的NH4+-N、通气正式培养 2周矿化出的NO3--N及碱解扩散出的NH4+-N ,其与小麦地上部吸N量之间的相关系数 (r)分别由淋洗前的0.443,0.119,0.259增加到淋洗后的 0.866 ,0.767,0.763。说明可矿化N反映土壤供N能力不佳是因为受起始NO3--N的干扰和影响，在土壤NO3--N含量较高的情况下，要正确评价可矿化N测定方法必须考虑NO3--N的作用。     

Inorganic nitrogen in a tropical soil with frequent amendments of sewage sludge

Accurate prediction of plant-available N release from sewage sludge is necessary to optimize crop yields and minimize NO₃^– leaching to groundwater. We conducted a 1.5-year study with three maize crops to determine N mineralization from an urban sewage sludge from Barueri, State of São Paulo, Brazil, and its potential to contaminate groundwater with NO₃^–. The soil at the experimental site was a loamy/clayey-textured Dark Red Dystroferric Oxisol. The treatments consisted of: plots without chemical fertilization or sludge, plots with complete chemical fertilization, and plots receiving four different doses of sewage sludge. Dose 1 was calculated at the agronomic N rate, while doses 2, 3 and 4 were, respectively, two, four, and eight times dose 1. The inorganic N addition increased with the rate of biosolid application. The high NO₃^– concentrations in relation to NH₄⁺ were associated with intense soil nitrification. High N losses occurred for the first 27 days after soil sludge incorporation, even at the lowest dose, suggesting that land application of sewage sludge based on the N requirement of the crop may be overestimating the amount of sewage sludge to be applied.     

Microbial and soil parameters in relation to N mineralization in soils of diverse genesis under differing management systems

 Oregon soils from various management and genetic histories were used in a greenhouse study to determine the relationships between soil chemical and biological parameters and the uptake of soil mineralized nitrogen (N) by ryegrass (Lolium perenne L.). The soils were tested for asparaginase, amidase, urease, β-glucosidase, and dipeptidase activities and fluorescein diacetate hydrolysis. Microbial biomass carbon (C) and N as well as metabolic diversity using Biolog GN plates were measured, as were total soil N and C, pH, and absorbance of soil extracts at 270 nm and 210 nm. Potentially mineralizable N (N₀) and the mineralization rate constant (k) were calculated using a first order nonlinear regression model and these coefficients were used to calculate the initial potential rate of N mineralization (N₀ k). Except for Biolog GN plates, the other parameters were highly correlated to mineralized N uptake and each other. A model using total soil N and β-glucosidase as parameters provided the best predictor of mineralized N uptake by ryegrass (R ² =0.83). Chemical and biological parameters of soils with the same history of formation but under different management systems differed significantly from each other in most cases. The calculated values of the initial potential rate of mineralization in some cases revealed management differences within the same soil types. The results showed that management of soils is readily reflected in certain soil chemical and biological indicators and that some biological tests may be useful in predicting N mineralization in soils. Received: 31 January 1997     

Cation exchange capacity measurements

Abstract

Soil cation exchange capacity (CEC) measurements are important criteria for soil fertility management, vaste disposal on soils, and soil taxonomy. The objective of this research was to compare CEC values for arable Ultisols from the humid region of the United States as determined by procedures varying widely in their chemical conditions during measurement. Exchangeable cation quantities determined in the course of two of the CEC procedures were also evaluated. The six procedures evaluated were: (1) summation of N NH₄OAc (pH 7.0) exchangeable Ca, Mg, K, and Na plus BaCl₂ ‐ TEA (pH 8.0) exchangeable acidity; (2) N Ca(OAc)₂ (pH 7.0) saturation with Mg(OAc)₂ (pH 7.0) displacement of Ca²⁺; (3) N NH₄OAc (pH 7.0) saturation with NaCl displacement of NH₄ ⁺; (4) N MgCl₂ saturation with N KCl displacement of Mg²⁺; (5) compulsive exchange of Mg²⁺ for Ba²⁺; and (6) summation of N NH₄OAc (pH 7.0) exchangeable Ca, Mg, K, and Na plus N KCl exchangeable AJ. The unbuffered procedures reflect the pH dependent CEC component to a greater degree than the buffered methods. The compulsive exchange and the summation of N NH₄OAc exchangeable cations plus N KCl exchangeable Al procedures gave CEC estimates of the same magnitude that reflect differences in soil pH and texture. The buffered procedures, particularly the summation of N NH₄OAc exchangeable cations plus BaCl₂ ‐ TEA (pH 8.0) exchangeable acidity, indicated inflated CEC values for these acid Ultisols that are seldom limed above pH 6.5. Exchangeable soil Ca and Mg levels determined from extraction with 0.1 M BaCl₂ were consistently greater than values for the N NH₄Oac (pH 7.0) extractions. The Ba²⁺ ion is apparently a more efficient displacing agent than the NH₄ ⁺ ion. Also, the potential for dissolving unreacted limestone is greater for the Ba₂ ⁺ procedures than in the NH₄ ⁺ extraction.     

Importance of organic nitrogen fractions in sandy soils,obtained by electro-ultrafiltration or CaCl2 extraction,for nitrogen mineralization and nitrogen uptake of rape

Summary Sandy soils have low reserves of mineral N in spring. Therefore organic-bound N is the most important pool available for crops. The objective of the present investigation was to study the importance of the organic-bound N extracted by electro-ultrafiltration and by a CaCl₂ solution for the supply of N to rape and for N mineralization. Mitscherlich-pot experiments carried out with 12 different sandy soils (Germany) showed a highly significant correlation between the organic N extracted (two fractions) and the N uptake by the rape (electroultrafiltration extract: r=0.76^***; CaCl₂ extract: r=0.76^***). Organic N extracted by both methods before the application of N fertilizer was also significantly correlated with N mineralization (electro-ultrafiltration extract: r=0.75^***; CaCl₂ extract: r=0.79^***). N uptake by the rape and the mineralization of organic N increased with soil pH and decreased with an increasing C:N ratio and an increasing proportion of sand in the soils. Ninety-eight percent of the variation in N uptake by the rape was determined by the differences in net mineralization of organic N. This show that in sandy soils with low mineral N reserves (NO _inf3 ^sup- -N, NH ₄ ⁺ -N) the organic soil N extracted by electro-ultrafiltration or CaCl₂ solutions indicates the variance in plant-available N. Total soil N was not related to the N uptake by plants nor to N mineralization.     

A method for determining microbially available N and P in an organic soil

Summary A bioassay of microbially available soil N and P is described. It is based on the addition of glucose together with N or P to soil, followed by monitoring of the respiration rate. The addition of glucose + N resulted in an immediate increase in the soil respiration rate followed by a short period of exponential increase, reflecting the growth of microorganisms on the added substrate. The exponential phase levelled off, when lack of P prevented further growth of the soil microorganisms. The soil respiration rate then remained constant for several hours before decreasing, when glucose became limiting. The addition of glucose + P resulted in a lower plateau of the soil respiration rate, indicating that microbial growth was more limited by N than P in this forest soil (0.28 and 0.79 mg CO₂ g^-1 organic matter h^-1, respectively). Additions of the limiting nutrient resulted in a proportional increase in the constant level of the soil respiration rate. This was used to calculated the increase in the soil respiration rate per mg N (0.71 mg CO₂ h^-1) or mg P (4.6 mg CO₂ h^-1) added to this particular soil. Microbially available N was then calculated in two ways from the regression equation (0.15 or 0.40 mg g^-1 organic matter) and P (0.13 or 0.17 mg g^-1 organic matter). A comparison with 2 M KCl extraction showed that in nutrient-poor forest soils the microbially available N was 6.3 or 18.5 times higher than the KCl extractable N.     

一种通用型土壤有效元素高效提取方法及应用

Mehlich 3（M3）方法可同时提取土壤中磷、钾、钙、镁、铝、铁、锌、锰、铜等多种元素的有效态，提高土壤检测的效率；另外，M3法适用于钙质土、火山灰土、高度风化土等各类土壤，可作为一个“通用”型土壤有效元素提取试剂。但是硝酸铵（NH4NO3）由于管制不易获取，应用M3方法测定土壤有效元素含量时受到极大限制。因此，本研究用另一种易获取的惰性电解质氯化铵（NH4Cl）替代硝酸铵（NH4NO3），评价氯化铵替代硝酸铵M3法的适用性。Pearson相关分析结果表明，用氯化铵替代硝酸铵M3法测得的30种土壤有效磷、钾含量与M3法测定结果呈极显著正相关，其决定系数（R2）分别为0.99（P=2.31×10-55，n=60）和0.98（P=1.52×10-49，n=60）。同时，氯化铵替代硝酸铵M3法和M3法测定的有效钙、镁、铝、铁、锌、锰和铜含量极显著相关，R2值分别为0.98，1.00， 0.99，0.96，0.99，0.95和0.94。氯化铵替代硝酸铵M3–P与酸性、中性和碱性土壤的 Bray–P和Olsen–P极显著相关，R2分别为0.97和0.91 （P=1.42×10-15和1.00×10-21，n=20和40）。同时，利用氯化铵替代硝酸铵M3法测定酸性改良土壤有效磷含量，发现其得到显著提高。因此，氯化铵替代硝酸铵M3法可作为测定各种土壤，以及改良土壤中有效磷、钾和其他金属元素有效态含量的通用方法。     

Influence of Sampling Date on Soil Nitrogen Availability Indices

In spite of the great effort that has been devoted to the search for a chemical laboratory index to predict nitrogen (N) mineralization capability of soils, the results have not yet been fully satisfactory. A continued effort is still needed to increase the knowledge of the sources of variation that influence potentially available soil N. The time of sampling has received little attention, taking into account its potential to influence N-mineralization patterns. In this work, soil samples from three different agrosystems, consisting of a double-crop sequence of small grains and maize, an intensively grazed pasture, and a rainfed olive orchard, were collected at different dates. Several chemical extractions were performed, and the results were correlated with N uptake by turnip (Brassica campestris, L.) grown in a pot experiment. Kjeldahl N was the chemical test that best correlated (R ² = 0.621) with N uptake by turnip. Kjeldahl N showed great versatility relative to the origin of the soil samples. However, it was not very sensitive to the time of sampling. It did not detect changes occurring in the soil over a short period of time. Soil inorganic N showed the second highest coefficient of correlation (R ² = 0.483) with N uptake by turnip. In contrast to that observed with Kjeldahl N, soil inorganic N appeared as an index that can vary greatly over the short term. The hot saline potassium chloride (KCl) extractions gave generally fair results. The poorest, however, were obtained with the ultraviolet absorption of extracts of 0.01 mol L^?1 sodium bicarbonate (NaHCO₃) measured at 250- and 260-nm wavelengths.