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1.
ABSTRACT

The accumulation of potentially toxic elements (PTEs) in the soil can pose risks to human health, and precise risk assessment dealing with the production and consumption of plants is required. The 0.43 M of nitric acid (HNO?) solution was suggested by the International Organization for Standardization for reactive fraction of PTEs in the soil. The efficiency of some extractors was evaluated in tropical soils. Contents of barium (Ba), cadmium (Cd), copper (Cu), nickel (Ni) and zinc (Zn) were extracted in accordance with the methods of Environmental Protection Agency (EPA) 3051A, Aqua Regia, Diethylenetriaminepentaacetic acid (DTPA), Mehlich-1, Mehlich-3, 0.43 M HNO? and 0.01 M of calcium chloride (CaCl?), and these contents correlated with the contents of PTEs in roots, shoots, and fruits of vegetables. Mehlich-3 had the highest correlation with Ni and Zn contents extracted by the plants. Contents extracted with 0.43 M HNO? had high correlation with the amounts extracted by DTPA and Mehlich-3, as well as with the amounts of PTEs accumulated by plants.  相似文献   

2.
Simultaneous multi-element extraction has been increasing worldwide to improve soil laboratory testing quality and effciency. This study sought to investigate the applicability of the Mehlich-1, Mehlich-3, and resin methods for simultaneous extraction of soil available P, K, Ca, and Mg as well as the effect of using conversion equations on nutrient recommendations for crops. Topsoil (0-20 cm) samples were taken from the most representative soil types used for crop production in southern Brazil with a wide range of chemical, physical, and mineralogical properties. Soil P, K, Ca, and Mg were simultaneously extracted using 1.0 mol L-1 KCl, Mehlich-1 and Mehlich-3 solutions, and membrane resin. The amounts of P extracted with the Mehlich-1 method were, on average, 50% lower than those extracted with the resin and Mehlich-3 methods. However, the resin method extracted the lowest amounts of K, Ca, and Mg. The use of conversion equations was suitable and it did not a?ect negatively the K recommendations for crops grown on soils of southern Brazil.  相似文献   

3.
The influence of soil properties on phosphorus (P) availability of Louisiana alluvial soils is not fully understood. A pot experiment was conducted in 2011 to evaluate the effect of different P fertilizer rate (0, 34, 67, 101 and 134 kg P2O5 ha?1) on corn growth and development on Perry clay and Commerce silt loam (sil) soils and relate Mehlich-3 and Bray-2 soil test P values with yield, total biomass, and P uptake of corn. The Bray-2 P values were six times higher than Mehlich-3 P values for Commerce sil while they were similar for Perry clay. Bray-2 and Mehlich-3 extractable-P of both soils increased with increasing P rate but only corn grown on Perry clay responded to P rate (P < 0.05). Implementation of appropriate testing procedure for estimating plant-available P in soil is an important component of effective P fertilization guidelines for corn.  相似文献   

4.
An incubation and a pot experiment were conducted to evaluate the dissolution and agronomic effectiveness of a less reactive phosphate rock, Busumbu soft ore (BPR), in an Oxisol in Kenya. Resin (anion and anion + cation)‐extractable P and sequentially extracted P with 0.5 M NaHCO3, 0.1 M NaOH, and 1 M HCl were analyzed. Dissolution was determined from the increase in anion resin (AER)–, NaHCO3‐, and NaOH‐extractable P in soil amended with PR compared with the control soil. Where P was applied, resin P significantly increased above the no‐P treatment. Busumbu‐PR solubility was low and did not increase significantly in 16 weeks. Anion + cation (ACER)‐extractable P was generally greater than AER‐P. The difference was greater for PR than for triple superphosphate (TSP). The ACER extraction may be a better estimate of plant P availability, particularly when poorly soluble P sources are used. Addition of P fertilizers alone or in combination with Tithonia diversifolia (TSP, BPR, TSP + Tithonia, and BPR + Tithonia) increased the concentration of labile inorganic P pools (NaHCO3‐ and NaOH‐Pi). Cumulative evolved CO2 was significantly correlated with cumulative N mineralized from Tithonia (r, 0.51, p < 0.05). Decrease in pH caused NH ‐N accumulation while NO ‐N remained low where Tithonia was incorporated at all sampling times. However, when pH was increased, NH ‐N declined with a corresponding rise in NO ‐N. Tithonia significantly depressed soil exchangeable acidity relative to control with time. A significant increase (p < 0.05) was observed for P uptake but not dry‐mass production in maize where BPR was applied. The variations in yield and P uptake due to source and rates of application were statistically significant. At any given P rate, highest yields were obtained with Tithonia alone. Combination of Busumbu PR with TSP or Tithonia did not enhance the effectiveness of the PR. The poor dissolution and plant P uptake of BPR may be related to the high Fe content in the PR material.  相似文献   

5.
We analyzed in soils with contrasting cultivation histories the depletion of P following sequential extractions with soil testing solutions. Soil samples were collected in three experiments in eastern Canada (L’Acadie, Lévis, and Normandin) and P was sequentially extracted 16 times, once daily, using Mehlich-3 (M3) or Olsen (Ol) solution. The cumulative amount of P extracted was 252 mg PM3 kg?1 and 77 mg kg?1 POl for L’Acadie, 212 mg PM3 kg?1 and 66 mg POl kg?1 for Lévis, and 424 mg PM3 kg?1 and 83 mg POl kg?1 for Normandin. The depletion of P was described by a logarithmic function (Y = a ln (N+ b) for PM3, and a power function (Y = αNβ) for POl. The inorganic P pool decreased in the three soils. The organic P pool did not decrease possibly because soil testing solutions did not directly extract P from this pool. This study demonstrated that laboratory soil testing analysis using M3 or Ol solution principally target P from the inorganic pool, suggesting that P fertilizer recommendations to mineral soils relying on these methods do not account for the potential of the organic P pool to contribute to soil P availability.  相似文献   

6.
Abstract

Acid and dilute‐salt chemical extractants are commonly used to assess and adjust phosphorus (P) availability in soils. Soybean was grown for 45 days under greenhouse conditions on samples of 10 Oxisols treated with variable levels of soluble P to compare critical soil P levels between an anion exchange resin (AER) and the Mehlich‐1 extractant, and to evaluate the influence of the soil P capacity factor (PCF) on the critical soil P levels. Variation among soils in the quantities of extracted P and critical P levels with the AER was less than that with Mehlich‐1. Low correlation values between soil characteristics related to PCF and measurements of AER soil P suggested that the AER method was not as sensitive to variations in soil PCF as Mehlich‐1. Interpretations of AER critical P levels, therefore, do not need auxiliary measures of PCF as with the Mehlich‐1 extractant. The reverse was true, however, for P uptake. Therefore, the criteria used to assess plant response to P (P uptake or dry matter production) in soils with variable PCF will influence the results obtained in correlations between methods used to extract soil P.  相似文献   

7.
Differences in soil phosphorus (P) contents measured by various techniques may have implications for agronomic and environmental testing. Reduced-tillage systems combined with surface manure application increase the potential risk of nutrient losses by surface runoff. A field trial was conducted to evaluate the effect of livestock slurry on nutrient accumulation at the surface layer of an acidic soil rich in organic matter with excess P levels and loamy texture. Two reduced-tillage systems, no tillage (NT) and minimum tillage (MT), and four different fertilizer treatments were assessed. The amounts of P extracted by anion-exchange resin (AER) and by Mehlich 3 (M3) were compared; in addition, differences between two determination methods of P contents extracted by Mehlich 3, namely molybdic acid colorimetric standard procedure (M3-COL) and inductively coupled plasma–mass spectroscopy (M3-ICP), were evaluated. Ninety-six soil samples were taken from the 0- to 5-cm surface layer in three successive dates after increasing manure addition. Colorimetric Mehlich 3 P ranged from 49 to 431 mg dm–3. The ranks of mean extractable soil P concentrations were AER < M3-COL < M3-ICP. The linear correlation coefficient between M3-COL and M3-ICP was highly significant (R2 = 0.89; P < 0.01), but a two-straight-lines model or a quadratic relationship were more adequate for describing the dependence between the two determination procedures after M3 extraction. Relative and absolute differences between M3-COL and M3-ICP showed a tendency to increase as organic carbon content increased. Phosphorus content extracted by AER and M3-COL or M3-ICP reported a significant but much less predictable relationship with R2 values of 0.27 and 0.21 (n = 96), respectively. The P in the surface layer accumulated more under NT than under MT.  相似文献   

8.
Lettuce (Lactuca sativa L.) and dry beans (Phaseolus vulgaris L.) were grown in three Brazilian Red-Yellow Latossols (Oxisols) in greenhouse conditions with cadmium (Cd), lead (Pb), copper (Cu), zinc (Zn), and nickel (Ni) applied to soils in treatments arranged as a randomized complete block design. Plant metals were analyzed in lettuce shoots and dry beans roots, stems, leaves, and seeds. After plant growth, soil samples from the pots were extracted with Mehlich-3 (M-3) for metal availability evaluation. The release of Ni in the M-3 extraction was dependent on the soil exchangeable aluminum (Al3 +). Mehlich-3 was efficient for determination of availability of Cd, Pb, Cu, Zn, and Ni for dry beans and availability of Cd and Ni for lettuce. The dry bean leaves Cd, Pb, Cu, Zn, and Ni were highly correlated with their recovering from soils with M-3. The same was observed for Cd and Ni in lettuce shoots and the M-3 recovered metals from soils.  相似文献   

9.
A hybrid anion resin was tested for in situ phosphorus (P) availability measurement in soils of two stands recovering from acidification and having different P-sorption characteristics. The phosphate (P-PO4) sorption capacity of the resin (before saturation) was 48 µmol g?1. Sorption and elution were tested under P-PO4 concentrations common in acidic soils (0–0.42 mmol l?1) either with or without the presence of sulfate (0.2 mmol l?1). The efficiency of P-PO4 sorption was independent of the sulfate and was 100 ± 0.2% (n = 56, ± SD). The P-PO4 recovery stabilized after six elution steps (each: 50 ml of 0.5 M sodium hydroxide, resin/solution 5:1). The efficiency of P-PO4 recovery was 80 ± 7% and was used to evaluate field measurements. We determined the amount of P-PO4 in the field using resin bags in three consecutive years. The results indicate that bioavailable P is negatively related to the soil ability to retain P.  相似文献   

10.
Phosphorus (P) in an high-pH soil may not be readily available to a crop, even though soil-testing procedures indicate high levels are present. A 2-year field study was conducted to determine corn yield responses to different rates of P fertilization as a function of soil-test P levels determined using the Mehlich-3 extractant. In 1 of the 2 years of this study, corn yields responded to P application across all soil P levels in a linear plateau fashion, indicating that P availability was limiting regardless of soil P levels. Where soil-test P was less than 40 mg kg?1, corn yields showed a quadratic response to rate of P applied both years, and when soil-test P was between 40 and 60 mg kg?1, corn yields showed a response only in the second year, when better growing conditions occurred. Soil-test P levels based on the Mehlich-3 extractant identified deficiencies in soil P availability to the crop, which could be corrected by P fertilization on a high-pH soil. Uptake efficiency of applied P was low, indicating that much of the P applied was not available to the crop.  相似文献   

11.
The effects of farmyard manure (FYM), Tithonia diversifolia (tithonia) and urea when applied alone or in combination with Minjingu phosphate rock (MPR), Busumbu phosphate rock (BPR) or triple superphosphate (TSP) on soil acidity, P availability, maize yields and financial benefits were evaluated at Bukura and Kakamega in western Kenya. A reduction in exchangeable acidity and Al was observed in most tithonia- and FYM-treated soils, but not with inorganic P sources when applied in combination with urea. The effectiveness in increasing available soil P followed the order; TSP > MPR > BPR among inorganic P sources, and FYM > tithonia among organic materials at both sites. At Bukura, a site higher in both available P and Al saturation compared with Kakamega, maize did not respond to inorganic P sources applied in combination with urea. Maize, however, responded when inorganic P sources were applied in combination with FYM or tithonia at this site. At Kakamega, maize responded to TSP but not to MPR or BPR when applied with urea. Application of TSP in combination with tithonia gave the highest maize yields at both sites. Of the tested technologies, only FYM when applied alone at Bukura was economically attractive.  相似文献   

12.
Abstract

Anion‐exchange resins (AER) have been used to determine plant available phosphorus (P) since the fifties and their results have shown strong relationships with plant growth and P uptake irrespective of soil properties. However, this procedure is still not widely used by laboratories because of difficulties in handling resin beads under routine conditions. New kinds and different shapes of resins are being produced each with specific characteristics that must be evaluated before use in laboratory procedures. Thus the objective of this work was to evaluate an AER manufactured in membranes reinforced with a Modacrylic fabric. These anion‐exchange membrane (AEM) sheets are commercially available, making them suitable for soil testing. The membranes were cut in pieces (1.0×7.5 cm) identified as AEM‐strips. The AEM‐strips were soaked in 0.5M HCl for a few days and transferred, after being rinsed with deionized water (DI), to 0.5M NaHCO3 to convert them to HCO3 form. The AEM‐strips and resin beads in nylon bags recovered 98.4 and 98.0% of the P content in an aqueous P solution, respectively. Three eluent solutions were evaluated with different shaking times. The 0.1M H2SO4 and 1.0M NaCl in 0.1M HCl were equally suitable for the molybdenum blue color development without any pH adjustment, while the pH of the 0.5M HCl was too low. The elution of P from the AEM‐strips was independent of time with a 15‐min shaking being adequate for removal of all P from the strips. A comparison of soil sample preparation demonstrated that it was not necessary to vigorously grind or sieve the soil to improve the repeatability of the results. The AEM‐strips were compared with other methods (Pi impregnated filter paper, Mehlich I and Bray 1) using 32 soils from Guatemala with widely varying physico‐chemical and mineralogical properties. Phosphorus extracted by the AEM and Pi procedures (similar principle) were highly correlated and gave similar results irrespective of soil type. The acid extraction (Mehlich I and Bray 1 methods) attacked soil components (apatites) resulting in higher and inconsistent amounts of P extracted which may not be available to plants; the correlation between these methods within soils of similar properties was good, but when all soils were considered together the relationship was not significant. This demonstrated that the acid extraction method for P is not suitable for soils containing apatites, while those based on a sink for P (AEM and Pi) can be applied irrespective of the type of soil.  相似文献   

13.
Twenty surface (0–15 cm) samples of acidic soils were analyzed for water soluble (WS), exchangeable (EX), lead displaceable (Pb-disp.), acid soluble (AS), manganese (Mn) oxide occluded (MnOX), organically bound (OB), amorphous Fe oxide occluded (AFeOX), crystalline iron (Fe) oxide occluded (CFeOX) and residual (RES) fractions of Mn, and also for extractable Mn in some common soil extractants: (diethylenetriaminepentaacetic acid (DTPA) (pH 7.3), DTPA (pH 5.3), AB-DTPA (pH 7.6), Mehlich-3 (pH 2.0), Modified Olsen, 0.005 M calcium chloride (CaCl2), 1 M magnesium chloride (MgCl2) and ion exchange resins. The WS-Mn fraction showed a significant and positive correlation with Mn extractable in DTPA (pH 5.3) and AB-DTPA (pH 7.6), while both WS-Mn and EX-Mn fractions correlated significantly and positively with Mn concentration and uptake by maize plants grown in these soils. The AB-DTPA (pH 7.6) and DTPA (pH 5.3) appeared suitable to assess the availability of Mn in acidic soils.  相似文献   

14.
Abstract

Phosphorus (P) loading of soils from the repeated application of manure and the associated loss of P to water systems is a serious and increasing problem in today's agricultural landscape. The hypothesis of this study was that the application of mineral amendments to manure might reduce P availability in manure and soil without affecting crop productivity. An incubation experiment was conducted to evaluate the ability of aluminum sulfate, ferric chloride or calcium hydroxide at 100 and 200 g kg?1 of manure to reduce phytoavailable (Mehlich-3 extractable) P in liquid dairy, laying hen and broiler chicken manure. Mehlich-3 extractable P was reduced from 59 to 97% in all manure treated with aluminum sulfate and ferric chloride. The calcium hydroxide treatment resulted in a Mehlich-3 extractable P reduction ranging from ?17 to 51%. A container experiment was then carried out to examine the effect of soil with pre-treated manure on timothy (Phelum pretense L.) growth and soil P levels. Timothy yields in all dairy manure treatments were 45–57% lower compared to an N–P–K control, but were not lower compared to the untreated manure control. Dairy manure + aluminum sulfate (200 g kg?1) reduced water-extractable P by 82% relative to the N–P–K control. All other manure and amendment treatment combinations were not statistically different from the N–P–K or the untreated soil controls in terms of water-extractable P, Mehlich-3 extractable P or grass yield. Significant reductions in Mehlich-3 extractable P were observed with the aluminum sulfate or ferric chloride amendments, while varied results were observed with the calcium hydroxide amendment. Results suggest that the use of manure amended with aluminum sulfate or ferric chloride has little effect on growth or P accumulation by timothy. Overall, this study demonstrated that mineral pre-treatment of manure can reduce the extractable P content of the manure and soil without negative effects on plant growth.  相似文献   

15.
应用离子交换树脂膜法评价缓释复合肥料供肥特性的研究   总被引:1,自引:0,他引:1  
在25℃连续恒温培养条件下,采用离子交换树脂膜(IERM)提取,测定了不同缓释复合肥料(SRCF)在土壤中的氮、磷、钾养分的供肥特性,并与盆栽水稻的养分吸收进行比较。结果表明:56.d内2种SRCF在土壤中NO3--N和NH4+-N养分的日均供应量占普通复合肥(NCF)的3.3%~58.1%,并以NH4+-NNO3--N;2种SRCF的H2PO4-和K+的日均供应量占磷、钾施用量分别为NCF的14.9%、23.2%和92.7%、64.5%。与NCF相比,SRCF氮素和磷素养分在土壤中释放具有明显的缓释作用。Elovich和抛物线扩散方程的b值可分别用来表征SRCF的NO3--N、H2PO4-和NH4+-N、K+养分在土壤中释放后被吸收的日均供肥量。用离子交换树脂膜法提取测定的SRCF养分在土壤中的供肥特性与该法测定的土壤本身养分的供肥特性相似。SRCF氮、磷、钾养分累积释放量与盆栽水稻氮、磷、钾养分吸收量呈显著或极显著的正相关(r=0.869~*0.994**)。用离子交换树脂膜提取测定和评价缓释复合肥料在土壤中养分的供肥特性是一种比较理想的方法。  相似文献   

16.
It is recommended to use ionic strength adjustment buffers to increase reading accuracy while measuring potassium (K+) concentrations in aqueous solutions by using ion-selective electrodes (ISEs). Three laboratory leachate column studies were conducted to evaluate the efficiency of two buffers, 2.5 M sodium perchlorate (NaClO4) and 2.5 M sodium chloride (NaCl), in measuring K+ concentrations in three media types (peat moss, Oxisols, and Mollisols soils). Three algae species, KCl, and KNO3 were applied to provide 112 and 336 kg K/ha. Leachate samples were collected to a total of 16 weeks and measured using a K-ISE. The K+ data from the three trials showed a highly significant (r ~ 0.99) correlation between the two buffers. T-Test results showed highly significant (P < 0.01) differences between unbuffered and the two buffered solutions. However, there were no significant differences between the two buffered solutions, under the peat moss, Oxisols, and Mollisols soils. The results suggest that the least expensive buffer of 2.5 M NaCl is as accurate as NaClO4 in such aqueous solutions.  相似文献   

17.
Abstract

In Oxisols, acidity is the principal limiting factor for crop production. In recent years, because of intensive cropping on these soils, deficiency of micronutrients is increasing. A field experiment was conducted on an Oxisol during three consecutive years to assess the response of common bean (Phaseolus vulgaris L.) under a no‐tillage system to varying rates of lime (0, 12, and 24 Mg ha?1) and boron (0, 2, 4, 8, 12, 16, and 24 kg ha?1) application. Both time and boron (B) were applied as broadcast and incorporated into the soil at the beginning of the study. Changes in selected soil chemical properties in the soil profile (0- to 10‐ and 10- to 20‐cm depths) with liming were also determined. During all three years, gain yields increased significantly with the application of lime. However, B application significantly increased common bean yield in only the first crop. Only lime application significantly affected the soil chemical properties [pH; calcium (Ca2+); magnesium (Mg2+); hydrogen (H+)+ aluminum (Al3+); base saturation; acidity saturation; cation exchange capacity (CEC); percent saturation of Ca2+, Mg2+, and potassium (K+); and ratios of exchangeable Ca/Mg, Ca/K, and Mg/K] at both soil depths (0–10 cm and 10–20 cm). A positive significant association was observed between grain yield and soil chemical properties. Averaged across two depths and three crops, common bean produced maximum grain yield at soil pHw of 6.7, exchangeable (cmolc kg?1) of Ca2+ 4.9, Mg2+ 2.2, H++Al3+ 2.6, acidity saturation of 27.6%, CEC of 4.1 cmolc kg?1, base saturation of 72%, Ca saturation of 53.2%, Mg saturation of 17.6%, K saturation of 2.7%, Ca/Mg ratio of 2.8, Ca/K ratio of 25.7, and Mg/K ratio of 8.6. Soil organic matter did not change significantly with addition of lime.  相似文献   

18.
In the present study, Olsen [0.5 M sodium bicarbonate (NaHCO3), pH 8.5] and resin–bicarbonate (HCO3) tests underestimated available phosphorus (P) in calcareous soils treated with gypsum (CaSO4). The reaction of CaSO4 and HCO3 ? ion or resin–HCO3 to form calcium carbonate (CaCO3) precipitate reduced the strength of the Olsen NaHCO3 extractant and resin–HCO3 strip for P extraction. The iron (Fe) oxide–impregnated filter paper (Pi strip) was independent of CaSO4 influence and thus correctly estimated soil‐available P with respect to plant response to soil‐available P. Two greenhouse experiments were conducted with maize and wheat grown on calcareous soils treated with different rates of CaSO4. The results confirmed that Olsen and resin–HCO3 tests should not be used to measure available P or labile P in the P fractionation scheme in the calcareous soils containing significant amounts of gypsum.  相似文献   

19.
The Mehlich 1 (M1) soil-test method has been used for soil phosphorus (P) extraction in southern Brazil. The objective of this work was to compare M1, Mehlich 3 (M3), and ionic exchange resin (resin) soil-test methods to evaluate the soil P available for crops and grasses in soils amended with phosphate rock (PR). Oxisol and Alfisol received triple superphosphate (TS) and PR. The M1 solution extracted greater P amounts in soils amended with PR compared with the M3 solution and resin methods. Lesser P amounts were extracted with the M3 solution. Crops yields were better associated with the P amounts extracted with M3 and resin methods in soils amended with PR. The results showed that M1 overestimates soil P availability to plants in soils amended with PR; the M3 solution best estimated the soil P available for crops and grasses in soils amended with PR.  相似文献   

20.
A new method for estimation of resin phosphorus (P) in arid soils was developed. Four extractants [hydrochloric acid (HCl), sulfuric acid, nitric acid, and sodium bicarbonate] at various concentrations were used by different ion exchange resins. The results clearly showed HCl was the best extractant at 1.0 N concentration and that 6 h was the optimum time for more adsorption. The optimum adsorption and extraction occurred at 200 rpm and 75 rpm, respectively. Basic anion exchange resin in chloride form was the best resin for P mobilization. A strong correlation (P < 0.001) with the P uptake by different arid crops (pearl millet, clusterbean) was observed. Resin P showed correlation with soil total P (P < 0.001), available and mineral P (P < 0.01), and soil organic P (P < 0.05). The present method for resin-P estimation is found to be an important tool to determine plant P availability and available soil P status under arid environments.  相似文献   

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