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1.
This study was carried out with the objective of evaluating the effect of citrate concentration on the extraction efficiency of some micronutrients from soil. Composite surface soil samples (0–20 cm) were collected from Eastern Harage Zone (Babile and Haramaya Districts), Wolaita Zone (Damot Sore, Boloso Bombe, Damot Pulasa and Humbo Districts) and Dire Dawa Administrative Council in purposive sampling. The treatments were arranged in completely randomized design (CRD) with three replications. A greenhouse pot experiment with soybean plant was conducted to determine the correlation between soil test methods and the selected micronutrients, such as iron (Fe), copper (Cu), manganese (Mn) and zinc (Zn) in the leaves of the plant. The results showed that, among the different citrate concentrations with strontium chloride (SrCl2) tested for the determination of available Fe, Mn and Zn, the highest correlation coefficients (r = 0.82, p < 0.05), (r = 0.96, p < 0.001) and (r = 0.98, p < 0.001) were found between the diethylenetriamine pentaacetic acid (DTPA) method and 0.02 M strontium chloride (SrCl2)-0.025 M citric acid extractant, respectively. Therefore, 0.02 M SrCl2-0.025 M citric acid extractant is considered to be the most effective for the determination of Fe, Mn and Zn in soils of the studied areas. Similarly, high correlation coefficients (r = 0.97, p < 0.001) were found between DTPA and 0.02 M SrCl2-0.05 M citric acid and (r = 0.88, p < 0.01) between DTPA and 0.02 M SrCl2-0.025 M citric acid extractants for the determination of available Cu from soils. Hence, the 0.02 M SrCl2-0.05 M citric acid extractant was shown to be the best for the determination of Cu in soils of the studied areas. However, considering the use of universal extractant, the 0.02 M SrCl2-0.025 M citric acid extractant could easily be adopted as a procedure for the determination of Fe, Cu, Mn and Zn for both agricultural and environmental purposes. The greenhouse experiment confirmed the result.  相似文献   

2.
This study investigated those soil factors related to iron (Fe) chlorosis between Fe status of peach leaves and some soil properties in the Antalya region of Turkey. The total Fe content of leaves was negatively correlated with soil pH and the organic matter content of the soils. Extractable Fe (by 1N HCl) was negatively correlated with the calcium carbonate (CaCO3) and bicarbonate (HCO3‐) content of the soils. In addition, both total‐ and extractable‐Fe contents of leaves were also negatively correlated with the copper (Cu) content of the soils. On the other hand, significant correlations were found among the Fe index, P/Fe ratio of leaves, and soil pH, phosphorus (P), zinc (Zn), and Cu content of the soils. It appears from these studies that high pH, and the CaCO3, HCO3‐, and Cu contents are effective soil factors affecting the availability of Fe and its uptake by the peach trees, and these soil factors were associated with severity of Fe chlorosis in the studied area.  相似文献   

3.
Abstract

Three different chemical extractants were evaluated as to their extraction efficiency for copper (Cu), zinc (Zn), lead (Pb), aluminium (Al), iron (Fe), chromium (Cr), manganese (Mn), potassium (K), magnesium (Mg), and calcium (Ca) on forest soil profiles from the Romanian Carpathians. The extractants were hot 14 M nitric acid (HNO3), 0.05 M hydrochloric acid (HCl), and 0.1 M sodium pyrophosphate. By comparing amounts extracted by 0.05 M HCl and 0.1 M sodium pyrophosphate relative to that dissolved by hot 14 M HNO3, some conclusions were drawn concerning the chemical forms of the metals in the extractable pool. The amount released by 0.05 M HCl was generally less than 10% of the HNO3‐extractable fraction but showed considerable variation among the elements studied. The relative amount extracted by pyrophosphate increased with organic‐matter content of the soils for Cu, Zn, Pb, Al, Fe, and Cr; stayed more or less constant for Mn, K, and Mg; and decreased for Ca. These findings are discussed with respect to the different binding forms of the metals in the soil and the processes affecting their mobility. From the present results, the metals were ranked as follows with respect to their ability to form organic complexes in natural soils: Cu>Cr, Pb>Ca>Al>Fe, Zn, Mn, K>Mg. However, the use of cold dilute HCl as a fractionation step may be questionable in cases of soils with a high content of substances possessing large neutralization capacity for protons.  相似文献   

4.
The relationships between potential laboratory indices for plant‐available nitrogen (N) and the plant N uptake in a pot experiment with ryegrass were assessed for 13 mineral soils and 2 peat soils. The methods included aerobic soil incubation, soil incubation in a bioreactor, hot potassium chloride (KCl)–extractable mineral N, 0.01 M calcium chloride (CaCl2)–extractable N, and N loss at heating. The indices for total plant‐available N accounted for 63–93% of the variance in N uptake in a statistical analysis with all soils (n = 15) and 27–89% for the mineral soils (n = 13). Most indices were not a direct quantitative measure of the plant N uptake. The N mineralization indices accounted for 57–86% of the variance in N mineralization for all soils and 5–50% for the mineral soils. Hot KCl‐extractable mineral N and 0.01 M CaCl2–extractable N were the most promising rapid indices for plant‐available N.  相似文献   

5.
To evaluate the available silicon (Si) content in agricultural soils in Japan and to investigate the determining factors of this content, we collected 180 soil samples from the surface layer of paddies and upland fields in Japan and determined their available Si contents. A phosphate buffer (PB; 0.02 M, pH 6.9) or an acetate buffer (AB; 0.1 M, pH 4.0) was used to extract available Si from the soil samples, and the Si concentrations in the extracts were determined by inductively coupled plasma-atomic emissions spectroscopy (ICP-AES). The total Si content and selected physicochemical properties were also determined for the soil samples. The median values of the available Si contents by the PB and AB methods were 48.8 and 79.7 mg kg?1 and corresponded to 0.017% and 0.027% of the total Si content, respectively. The overall data showed log-normal distributions. The available Si content of the upland soils was significantly higher than that of the paddy soils by both the PB (p < 0.01) and AB methods (p < 0.05). The available Si contents by the PB and AB methods had a significant positive correlation (p < 0.01) and they had significant negative correlation with the total Si content (p < 0.01). The values of the available Si contents by the PB and AB methods correlated positively with the pH, total carbon (C) content, and dithionite-citrate bicarbonate extractable iron (Fed) and aluminum (Ald), acid oxalate extractable iron (Feo) and aluminum (Alo), Fed-Feo and Alo+1/2Feo values (p < 0.01). A multi-regression analysis indicated that pH, amorphous minerals and crystalline iron (Fe) oxides were the dominant determining factors of available Si in the soils, and these three variables explained approximately two thirds of the variation of available Si content in agricultural soils in Japan. In terms of soil type, Terrestrial Regosols, Dark Red soils and Andosols had relatively high available Si contents, whereas Sand-dune Regosols, Red soils and Gray Lowland soils had relatively low contents. In terms of region, the soils in the Kanto and Okinawa regions had relatively high available Si contents and those in the Kinki, Shikoku and Chugoku regions had relatively low contents. In conclusion, the available Si content and its determining factors for agricultural soils in Japan were quantitatively elucidated, and this will contribute to the establishment of rational soil management?—including the application of silicate materials, taking into account the Si-supplying power of the relevant soils—for sustainable and productive agriculture in Japan.  相似文献   

6.
Carbohydrates are an important component of soil organic matter, and a method is needed to quantify them, which would be efficient in terms of time and cost. Different extractants and methods were examined in this work for their efficiency to extract carbohydrate C from four calcareous soils. Four extractants (distilled water, 0.5 M potassium sulfate (K2SO4), and 0.25 and 0.5 M sulfuric acid (H2SO4)) and three incubation methods (shaking for 16 h, heating in an oven (85 °C) for 16 h, and heating in a water bath (85 °C) for 2.5 h) were compared. The results show that significantly more carbohydrate C was extracted from all four soils with oven and water bath heating of the soil–extractant suspensions than with shaking them at room temperature. The efficiency of the extractants decreased in this order: 0.5 M H2SO4 > 0.25 M H2SO4 > 0.5 M K2SO4. The combination of the heated–water bath incubation method with 0.5 M H2SO4 as extractant was the most efficient method.  相似文献   

7.
Abstract

A routine soil test that accurately predicts soil nitrogen (N) mineralization has long eluded researchers. Soil incubations, which are not practical for routine soil testing, are the only methods that have proven successful. Although several quick analytical methods have been proposed, no one method has correlated consistently enough to be implemented into a soil‐testing program. The objective of this study was to compare proposed quick analytical procedures with the amount of ammonium (NH4)‐N mineralized after a 14‐d anaerobic incubation. The analytical methods of interest were

  1. applying a mild acid oxidation to the soil using acidified permanganate;

  2. analyzing a 1 M potassium chloride (KCl) soil extract in the ultraviolet (UV) spectrophotometric range before and after nitrate (NO3) removal with Devarda's alloy; and

  3. quantifying soil amino sugar‐N content using the Illinois soil N test (ISNT) diffusion method.

Fifty agricultural soils with different physical and chemical properties were utilized in this study. All methods displayed significant relationships with the anaerobic incubation procedure; however, some methods displayed higher, more acceptable, coefficients of determination. The ISNT and UV spectrophotometry measurement at 210 nm after NO3 removal failed to accurately estimate N mineralization (R2=0.45 and 0.31, respectively). The acid oxidation procedure and UV measurement at 260 nm of soil extracts before NO3 removal produced better results with coefficients of determination of 0.58 and 0.56, respectively. We suspect the ability of some methods to predict N mineralization was hindered because of the wide variety of geographic locations from which the soils were collected. Additional analyses were conducted on a subset of 16 silt‐loam soils from Arkansas. The coefficient of determinations increased for each method: acid oxidation procedure increased to 0.83, the ISNT increased to 0.71, and the UV method (at 260 nm before NO3 removal) increased to 0.63. If anaerobic incubation is a true indication of N mineralization in the field, the aforementioned methods display promise to correlate with N uptake by field‐grown plant studies when adapted to a specific geographic location and/or soil series.  相似文献   

8.
Abstract

More than 90% of the nitrogen (N) in soils is bond as organic N compounds. The available N can be estimated on the mineral N released during time‐consuming incubations of soil. Several chemical methods have been developed as substitutes for incubations. On the other hand, there has been an increase in waste production. Residues could potentially offset the need for mineral fertilizers, being both an economic and environmental benefit. Thus, the development of a routine method for prediction of N supply both from soil organic matter (SOM) and the application of organic residues is of great interest. An incubation experiment was performed in a Cambic Arenosol to evaluate different chemical methods. Air‐dried soil was mixed with increasing amounts of composted solid municipal waste, secondary pulp‐mill sludge, hornmeal, poultry manure, the solid phase from pig slurry, and composted pig manure. Samples were incubated for 244 days under a controlled environment. Among the chemical extractants studied, hot 2 M potassium chloride (KCl) and hot 0.01 M calcium chloride (CaCl2) showed promise in indicating values of N0 (potentially available nitrogen), and these simple methods are suitable for use in routine laboratory conditions.  相似文献   

9.
Accurate estimation of the available potassium (K+) supplied by calcareous soils in arid and semi‐arid regions is becoming more important. Exchangeable K+, determined by ammonium acetate (NH4OAc), might not be the best predictor of the soil K+ available to crops in soils containing micaceous minerals. The effectiveness of different extraction methods for the prediction of K‐supplying capacities and quantity–intensity relationships was studied in 10 calcareous soils in western Iran. Total K+ uptake by wheat grown in the greenhouse was used to measure plant‐available soil K+. The following methods extracted increasingly higher average amounts of soil K+: 0.025 M H2SO4 (45 mg K+ kg?1), 1 M NaCl (92 mg K+ kg?1), 0.01 M CaCl2 (104 mg K+ kg?1), 0.1 M BaCl2 (126 mg K+ kg?1), and 1 M NH4OAc (312 mg K+ kg?1). Potassium extracted by 0.01 M CaCl2, 1 M NaCl, 0.1 M BaCl2, and 0.025 M H2SO4 showed higher correlation with K+ uptake by the crop (P < 0.01) than did NH4OAc (P < 0.05), which is used to extract K+ in the soils of the studied area. There were significant correlations among exchangeable K+ adsorbed on the planar surfaces of soils (labile K+) and K+ plant uptake and K+ extracted by all extractants. It would appear that both 0.01 M CaCl2 and 1 M NaCl extractants and labile K+ may provide the most useful prediction of K+ uptake by plants in these calcareous soils containing micaceous minerals.  相似文献   

10.
The potential of Nostoc 9v for improving the nitrogen (N)2–fixing capacity and nutrient status of semi‐arid soils from Tanzania, Zimbabwe, and South Africa was studied in a laboratory experiment. Nostoc 9v was inoculated on nonsterilized and sterilized soils. Inoculum rates were 2.5 mg dry biomass g?1 soil and 5 mg dry biomass g?1 soil. The soils were incubated for 3 months at 27 °C under 22 W m2 illumination with a photoperiod of 16 h light and 8 h dark. The moisture was maintained at 60% of field capacity. In all soils, Nostoc 9v proliferated and colonized the soil surfaces very quickly and was tolerant to acidity and low nutrient availability. Cyanobacteria promoted soil N2 fixation and had a pronounced effect on total soil organic carbon (SOC), which increased by 30–100%. Total N also increased, but the enrichment was, in most soils, comparatively lower than for carbon (C). Nitrate and ammonium concentrations, in contrast, decreased in all the soils studied. Increases in the concentration of available macronutrients were produced in most soils and treatments, ranging from 3 to 20 mg phosphorus (P) kg?1 soil, from 5 to 58 mg potassium (K) kg?1 soil, from 4 to 285 mg calcium (Ca) kg?1, and from 12 to 90 mg magnesium (Mg) kg?1 soil. Positive effects on the levels of available manganese (Mn) and zinc (Zn) were also observed.  相似文献   

11.
Zinc (Zn) distribution in different soil aggregates can affect Zn availability. In this study, the effect of soil aggregate-size fractions on Zn distribution and availability was determined in some heavy metal-contaminated soils. Air-dried samples were fractionated into four different aggregate-size fractions (2.0–4.0, 0.25–2.0, 0.05–0.25 and <0.05 mm). Extraction efficiency of available Zn determined by using Mehlich-3, DTPA-TEA, Mehlich-1 and H2O methods in different aggregates and relation between extracted Zn and corn indices were studied. Moreover, the Tessier fractionation scheme was applied to determine the partitioning of Zn in different aggregates. Among all the extractants, Mehlich-3 showed better extractability of Zn from soils and the highest amount of extracted Zn was found in the <0.05 (87.65 mg kg?1) and 0.05–0.25 (80.86 mg kg?1) mm fractions. Zn extracted by Mehlich-3 and DTPA-TEA in the <0.05 and 0.05–0.25 mm fractions had significant correlation with the amount of Zn in corn. Also, correlation coefficients between carbonate-bound and Fe–Mn oxide-bound Zn and available Zn in <0.05 and 0.05–0.25 mm aggregates was higher than other aggregates, suggesting that this two fraction of Zn in finer aggregates constituted the major available Zn pools in the studied soils.  相似文献   

12.
Evaluation of nutrient status in soil is important for nutritional, environmental, and economical aspects. The objective of this work was to find out the most suitable universal extractant for determination of available phosphorus (P) and nitrate (NO3-) and exchangeable potassium (K), calcium (Ca), and magnesium (Mg) from soils using 0.01 M calcium chloride (CaCl2), 0.01 M barium chloride (BaCl2), 0.1 M BaCl2, 0.02 M strontium chloride (SrCl2), Mehlich 3, and ammonium bicarbonate diethylene triamine penta acetic acid (AB-DTPA) extractants. Composite surface soil samples (0–20 cm) were collected from the Eastern Harage Zone (Babile and Haramaya Districts), Wolaita Zone (Damot Sore, Boloso Bombe, Damot Pulasa, and Humbo Districts), and Dire Dawa Administrative Council by purposive sampling. The experiment was carried out in a completely randomized design (CRD) with three replications. Results indicated that the greatest correlations were found between Mehlich 3 and Olsen method and also between 0.02 M SrCl2 and Olsen method for available P. The amount of NO3– extracted by 0.02 M SrCl2 was significantly correlated to the amount determined by 0.5 M potassium sulfate (K2SO4). The amounts of exchangeable K, Ca, and Mg determined by ammonium acetate (NH4OAc) method were significantly correlated to the amount determined by universal extractants tested. In general, both 0.02 M SrCl2 and Mehlich 3 can serve as universal extractants for the macronutrients considered in this study with the former being more economical when NO3– is included.  相似文献   

13.
(pp. 833–841)

In order to learn the status of available soil nitrogen (N), two sequential extraction methods (A and B) were tested. Proposed methods are as follows.

(A) Extraction with water, KCl, acetic acid, 1/15 M phosphate buffer, sulfuric acid, and NaOH.

(B) Extraction with water, KCl, 0.01 M sulfuric acid, 0.1 M sulfuric, 0.2 M sulfuric acid and 0.4 M sulfuric acid.

1) NO3-N was only detected in a solution extracted with water. Major N in an extract with KCl was in ammonium form. Extracts with phosphate buffer and sulfuric acid contained organic-N only. When these two fractions were examined by size exclusion chromatography (HPLC-SEC), only one major peak in each extract appeared.

2) Minerals, such as Al and Fe in each extract were determined using ICP (Varian Co., Ltd.). With the increase in concentration of sulfuric acid, the high Fe concentration in each extract increased. On the other hand, much higher Al was found in extracts with lower concentrations of sulfuric acid compared to Fe.

3) Though some crop species such as spinach and carrot show the potential to take up organic-N in a soil applied with organic matter, this sequential soil-nitrogen extraction method may be useful to evaluate availability of soil nitrogen fertility with more accuracy compared to conventional methods in the case of these superior crop species.  相似文献   

14.
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 (ΔNi) 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.  相似文献   

15.
Abstract

A study was conducted to investigate the chemical speciation of added cadmium (Cd) and lead (Pb) and their availability as influenced by fresh organic matter (OM) and sodium chloride (NaCl) in three agricultural soils. The soils were treated with 20 mg Cd/kg as cadmium nitrate [Cd(NO3)2 · 4H2O], 150 mg Pb/kg as lead nitrate [Pb(NO3)2], 20 g/kg alfalfa powder, and 50 mmol/kg of NaCl and then incubated for 3 months at 60% water‐holding capacity (WHC) and constant temperature (25 °C). Subsamples were taken after 1, 3, 6, and 12 weeks of incubation, and electrical conductivity (EC), pH, dissolved organic carbon (DOC), and concentrations of cations and anions were determined in the 1:2.5 soil/water extract. Available Cd and Pb were determined in 0.05 M ethylenediaminetetraacetic acid (EDTA) extract. Concentrations of organic and inorganic species of Cd and Pb in soil solution were also predicted using Visual Minteq speciation program. The most prevalent species of dissolved Pb and Cd in the soils were Pb‐DOC and Cd2+ species, respectively. Salinity application increased the available and soluble Cd significantly in the acid and calcareous soils. It, however, had little effect on soluble Pb and no effect on available Pb. Organic‐matter application decreased availability of added Pb significantly in all soils. In contrast, it raised soluble Pb in all soils except for the acid one and approximated gradually to the added Pb with time. Impact of OM on available Cd was somewhat similar to that of Pb. Soluble Cd increased by OM application in the calcareous soil, whereas it decreased initially and then increased with time in the other soils.  相似文献   

16.
Abstract

A study was carried out to investigate the status of four micronutrients, iron (Fe), copper (Cu), manganese (Mn), and zinc (Zn), and five other trace elements, cobalt (Co), chromium (Cr), nickel (Ni), lead (Pb), and strontium (Sr), in paddy soils of Bangladesh. Soil samples were digested by hydrofluoric acid (HF)‐nitric acid (HNO3)‐perchloric acid (HClO4) for determination of total contents of the nine elements, while DTPA, ASI and 0.1 Mhydrochloric acid (HC1) methods were used for determination of available Fe, Cu, Mn, and Zn. Total trace element contents were found to vary with physiography on which soils are distributed. In general, Ganges Tidal Floodplain soils had the highest content, whereas terrace soils had the lower content. Among the soil properties examined, clay content had a good relation with total trace element contents in the topsoil, except for Sr. Based on the variation with physiography or clay content, the nine trace elements could be grouped into six groups: Cu, Fe and Zn, Pb, Co and Cr and Ni, Mn, Sr. According to the extractable levels of four micronutrients, Bangladesh paddy soils had the medium to optimum amounts of Fe and Cu, but were deficient sporadically in Mn and extensively in Zn. It was indicated that paddy soils of Bangladesh are yet to be polluted with heavy metals.  相似文献   

17.
The usefulness of Mehlich 3 (M3) reagent was evaluated as a method to extract numerous elements from coalmine soils in As Pontes (Spain) showing a wide range of physicochemical properties. Critical levels (deficiency and/or toxicity) were established for plant available elements extracted by this reagent. The M3 method was compared to 1M NH4Cl, Olsen, acid oxalate, and DTPA methods as extractants for exchangeable Ca, Mg and K, available P, non-crystalline aluminium, and available heavy metals, respectively. The M3 method correlated significantly to NH4Cl for Ca, Mg and K (r=0·76, 0·84 and 0·87, respectively), to Olsen P (r=0·77) and to oxalate Al (r=0·77). Significant correlations were found between Fe, Cu, Zn and Cd extracted by M3 and DTPA; for Mn, Ni, Co and Pb different relationship between methods were obtained for acid and alkaline samples, so that critical levels were established for M3 metals as a function of soil pH. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

18.
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.  相似文献   

19.
Abstract

Plants commonly suffer from phosphorus (P) deficiency in calcareous soils. Plant responses to P application on such soils mostly show poor correlation with their soil test P values. Experiments were conducted on 24 different soil samples under laboratory and greenhouse conditions to illustrate the relationship of various inorganic P fractions in different calcareous soils with P uptake by plants, P extraction by iron‐impregnated filter paper, and P soil test values estimated by 0.5M NaHCO3 and ammonium bicarbonate diethylene triamine penta‐acetic acid. Total P in the 24 soils ranged from 652 to 1245 mgkg?1 with a mean of 922 mgkg?1. A major proportion (98%) of inorganic P was in HCl‐P (Ca‐bound) form. The HCl‐P (Ca‐bound) ranged from 296 to 729 with a mean of 480 mgkg?1. The iron (Fe) and aluminum (Al)‐P (NaOH‐P) ranged from 0.92 to 12 mgkg?1 with a mean of 1.57 mgkg?1. The Fe‐P (citrate‐dithionite bicarbonate) ranged from 0.22 to 4.40 mgkg?1 with a mean of 5.99 mgkg?1. Data regarding P release from the soil matrix obtained by desorption with iron‐impregnated filter paper was best described by the Elovich equation. Range of slope and intercept values were found to be 5.48 to 17.3 and 17.23 to 56.27 mgkg?1, respectively. Intercept values calculated for the Elovich equation may be related to labile P initially available for plant uptake in soils. Intercept values calculated for the Elovich equation correlated (r=0.77) significantly (p<0.01) with NaHCO3 extractable (Olsen‐P)P. Significant correlation (p<0.05) of intercept with CDB‐P (r=0.44) and of slope with HCl‐P (0.43) suggested that the initially available P, regulated through CDB‐P, is replenished by HCl‐P [calcium (Ca) bound].  相似文献   

20.
Abstract

To evaluate the content of nitrogen (N) fractions of agricultural soils in Java, Indonesia, in relation to soil type and land use, 46 surface soil samples, 23 from paddy and 23 from upland, were collected throughout Java to include various types of soils. Soil N was separated into four fractions according to form and availability: inorganic extractable nitrogen (Iex-N), fixed ammonium nitrogen (Ifix-N), organic mineralizable nitrogen (Omin-N) and organic stable nitrogen (Osta-N). The total-N content was determined by the dry combustion method. The Iex-N content was determined by extraction with a 2 mol L?1 potassium chloride (KCl) solution and the Ifix-N content by extraction with an hydrofluoric and hydrochloric acid (HF-HCl) solution after removal of organic-N. The Omin-N content was evaluated as the potentially mineralizable N based on a long-term incubation method. The Osta-N content was calculated as the difference between the contents of total-N and the three other fractions. The total-N content was 2.06 g kg?1 on average. The contents of Iex-N, Ifix-N, Omin-N and Osta-N were 25.8, 99.1, 103 and 1,832 mg kg?1, respectively, and corresponded to 1.3, 4.8, 5.0 and 88.9% of the total-N. Hence, available (Iex-N and Omin-N) and stable (Ifix-N and Osta-N) fractions accounted for 6.3% and 93.7% of the total-N, respectively. Correlation analysis indicated that the contents of total-N and Osta-N had positive correlation with (Alo + 1/2Feo) as an index of amorphous minerals (p < 0.01), suggesting strong influence of volcanic materials for the accumulation of organic matter in Java soils. The content of Ifix-N had a positive correlation with nonexchangeable potassium (K) content (p < 0.01), suggesting the contribution of 2:1 clay minerals which can fix both ammonium (NH4+) and K+ in their interlayer sites. On the contrary, Omin-N did not have any significant correlation with soil properties, implying the importance of management for the improvement of the available N level in soils, rather than intrinsic soil properties. Soil N status further showed strong topographical trends depending on the elevation where soil developed. The contents of total N, Iex-N, Ifix-N, Omin-N and Osta-N in Java soils were on average 80, 69, 90, 65 and 80% of those in Japanese soils, respectively, suggesting that the soil N level in Java was lower than that in Japan, probably due to accelerated decomposition of organic matter, especially degradable fractions, reflecting high temperature, but that the level was relatively high for tropical soils due to the effect of volcanic materials. In conclusion, these results should be taken into account for the sustainable management of soil N in agricultural fields in Java, Indonesia.  相似文献   

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