Heavy metal concentration in forage grasses and extractability from some acid mine spoils

Laboratory and greenhouse studies were conducted on several forage grasses, bermudagrass (Cynodon dactylon), creeping red fescue (Festuca rubra), Kentucky 31-tall fescue (Festuca arundinacea), oat (Avena sativa), orchardgrass (Dactylis glomerata), perennial ryegrass (Lolium perenne), sorghum (Sorghum bicolor), triticale (X. triticosecale Wittmack), and winter wheat (Triticum aestivum) grown on three Alabama acid mine spoils to study heavy metal accumulation, dry matter yield and spoil metal extractability by three chemical extractants (Mehlich 1, DTPA, and 0.1 M HCl). Heavy metals removed by these extractants were correlated with their accumulation by several forage grasses. Among the forages tested, creeping red fescue did not survive the stressful conditions of any of the spoils, while orchard grass and Kentucky 31-tall fescue did not grow in Mulberry spoil. Sorghum followed by bermudagrass generally produced the highest dry matter yield. However, the high yielding bermudagrass was most effective in accumulating high tissue levels of Mn and Zn from all spoils (compared to the other grasses) but did not remove Ni. On the average, higher levels of metals were extracted from spoils in the order of 0.1 M HCl>Mehlich 1>DTPA. However, DTPA extracted all the metals from spoils while Mehlich 1 did not extract Pb and 0.1 M HCl did not extract detectable levels of Ni. All of the extractants were quite effective in determining plant available Zn from the spoils. For the other metals, the effective determination of plant availability depended on the crop, the extractant, and the metal in concert.     

Residual heavy metal concentrations in sludge‐amended coastal plain soils ‐ I. Comparison of extractants

Abstract

The purposes for this research were: to examine the long‐term residual effects of farmland applications of municipal sludges from four treatment technologies on the total and extractable Zn, Cu, Mn, Fe, Pb, Ni and Cd concentrations in Coastal Plain soils; to investigate the effects of sludge sources and rates on the effectiveness of soil extractants to remove the various metals; and to determine correlation coefficients for soil extractable versus plant accumulation in tobacco. The extractants evaluated were Mehlich 1 and 3, and DTPA‐pH 7.3. Composite Ap horizon soil samples and tobacco leaf samples were obtained in 1984 from research plots at two sites in Maryland that were established in 1972 and 1976, respectively, using sludge materials from three wastewater treatment facilities in the Washington, D.C. metropolitan region. Similar application rates were used at both sites.

A wide range in soil pH values was found among treatments at each site. Significant (p ≤ 0.05) increases were observed in total Zn, Cu, Fe, Pb, Ni, and Cd for all sludge sources with increased rates; however, values for total soil Mn exhibited high variability in all cases. The rankings among the extractants varied for some elements depending on the sludge sources. For Zn, the rankings were Mehlich 1 > Mechlich 3 > DTPA‐pH 7.3 across all sources and rates. For Cu, Mehlich 3 > Mehlich 1 > DTPA‐pH 7.3 was found for soils amended with Blue Plains digested (BPD) and Piscataway limeddigested (PLD) sludges but Mehlich 1 ≥ DTPA pH 7.3 > Mehlich 3 for Blue Plains limed compost (BPLC) and Annapolis Fe and heat treated (AFH) sludges. Concerning extractable Mn, Mehlich Mehlich 1 > Mechlich 3 > DTPH pH 7.3 was the order for BPLC and AFH sludges but Mehlich 3 > Mehlich 1 > DTPA‐pH 7.3 was observed for BPD and PLD sludges. The rankings among extractants for Fe (Mehlich 3 > Mehlich 1 > DTPA‐pH7.3), Ni (Mehlich 3 ≥ Mehlich 1 > DTPA‐pH 7.3), Pb (Mehlich 3 > DTPA‐pH 7.3 > Mehlich 1) and Cd (Mehlich 1 > Mehlich 3 > DPTA‐pH7.3) were somewhat similar across all sludge sources. Significant correlation coefficients were obtained for all three extractants for soil extractable vs. plant Zn, Cu, Ni, and Cd at both sites; however, Mehlich 3 was not significant for Mn. Also, neither of the extractants produced significant coefficients for Fe and Pb.     

Soil Test to Predict the Copper Availability in Pasture Soils

Abstract

The proportion of copper (Cu) that can be extracted by soil test extractants varied with the soil matrix. The plant‐available forms of Cu and the efficiency of various soil test extractants [(0.01 M Ca(NO₃)₂, 0.1 M NaNO₃, 0.01 M CaCl₂, 1.0 M NH₄NO₃, 0.1 M HCl, 0.02 M SrCl₂, Mehlich‐1 (M1), Mehlich‐3 (M3), and TEA‐DTPA.)] to predict the availability of Cu for two contrasting pasture soils were treated with two sources of Cu fertilizers (CuSO₄ and CuO). The efficiency of various chemical reagents in extracting the Cu from the soil followed this order: TEA‐DTPA>Mehlich‐3>Mehlich‐1>0.02 M SrCl₂>0.1 M HCl>1.0 M NH₄NO₃>0.01 M CaCl₂>0.1 M NaNO₃>0.01 M Ca(NO₃)₂. The ratios of exchangeable: organic: oxide bound: residual forms of Cu in M1, M3, and TEA‐DTPA for the Manawatu soil are 1:20:25:4, 1:14:8:2, and 1:56:35:8, respectively, and for the Ngamoka soil are 1:14:6:4, 1:9:5:2, and 1:55:26:17, respectively. The ratios of different forms of Cu suggest that the Cu is residing mainly in the organic form, and it decreases in the order: organic>oxide>residual>exchangeable. There was a highly significant relationship between the concentrations of Cu extracted by the three soil test extractants. The determination of the coefficients obtained from the regression relationship between the amounts of Cu extracted by M1, M3, and TEA‐DTPA reagents suggests that the behavior of extractants was similar. But M3 demonstrated a greater increase of Cu from the exchangeable form and organic complexes due to the dual activity of EDTA and acids for the different fractions and is best suited for predicting the available Cu in pasture soils.     

Soil test for available zinc in acid soils of Venezuela

Abstract

Zinc (Zn) deficiencies have been identified in Venezuela with increasing frequency in recent years. However, there are no established critical values for available Zn in the acid soils of this country. Greenhouse studies were initiated to evaluate five extractants, DTPA, DTPA‐HCl, Na‐EDTA, 0.1N hydrochloric acid (HCl), and Mehlich 1 to predict Zn availability in 14 acid soils with corn as the test crop. Significant and positive correlations were found between Zn extracted among the five extractants. Zinc extracted was not related with soil pH and organic matter content, but with the cation exchange capacity and clay content. The Na‐EDTA extractant was found to be the most suitable as an indicator of Zn‐deficient acid soils, the critical Zn value being 2.4 mg#lbkg^‐1.     

Use of Single Extraction Methods to Predict Bioavailability of Heavy Metals in Polluted Soils to Rice

Human exposure to toxic heavy metals via dietary intake is of increasing concern. Heavy-metal pollution of a rice production system can pose a threat to human health. Thus, it was necessary to develop a suitable extraction procedure that would represent the content of metal available to rice plants (Oryza sativa L.). The aim of this study was to predict, on the basis of single extraction procedures of soil heavy metals, the accumulation of heavy metals (cadium, lead, copper, and zinc) in rice plants. Six extracting agents [Mehlich 1, Mehlich 3, EDTA (ethylenediaminetetraacetic acid), DTPA–TEA (diethylenetriaminepentaacetic acid–triethanolamine), ammonium acetate (NH₄OAc), and calcium chloride (CaCl₂)] were tested to evaluate the bioavailability of heavy metals from paddy soils contaminated with lead–zinc mine tailings to rice. The extraction capacity of the metals was found to be of the order EDTA > Mehlich 3 > Mehlich 1 > DTPA–TEA > NH₄OAc > CaCl₂. The correlation analysis between metals extracted with different extractants and concentrations of the metals in the grain and stalk of the plant showed positive correlations with all metals. The greatest values of correlation coefficients were determined between the NH₄OAc- and CaCl₂-soluble fractions of soil and contents in plants in all four metals studied. Therefore, NH₄OAc and CaCl₂ were the most suitable extractants for predicting bioavailability of heavy metals in the polluted soils to rice. The results suggested that uptake of heavy metals by rice was mostly from exchangeable and water-soluble fractions of the metals in the soils. Soil-extractable metals were more significantly correlated with metal accumulation in the stalk than in the grain. The pH had more significant influence on availability of heavy metals in the soils than total content of metals and other soil properties. The bioavailability of metals for rice plants would be high in acidic soils.     

Comparison of routine soil tests and EPA method 3050 as extractants for heavy metals in Delaware soils

Abstract

Agricultural use of sewage sludges can be limited by heavy metal accumulations in soils and crops. Information on background levels of total heavy metals in soils and changes in soil metal content due to sludge application are; therefore, critical aspects of long‐term sludge monitoring programs. As soil testing laboratories routinely, and rapidly, determine, in a wide variety of agricultural soils, the levels of some heavy metals and soil properties related to plant availability of these metals (e.g. Cu, Fe, Mn, Zn, pH, organic matter, texture), these labs could participate actively in the development and monitoring of environmentally sound sludge application programs. Consequently, the objective of this study was to compare three soil tests (Mehlich 1, Mehlich 3, and DTP A) and an USEPA approved method for measuring heavy metals in soils (EPA Method 3050), as extractants for Cd, Cu, Ni, Pb and Zn in representative agricultural soils of Delaware and in soils from five sites involved in a state‐monitored sludge application program.

Soil tests extracted less than 30% of total (EPA 3050) metals from most soils, with average percentages of total metal extracted (across all soils and metals) of 15%, 32%, and 11% for the Mehlich 1, Mehlich 3, and DTPA, respectively. Statistically significant correlations between total and soil test extractable metal content were obtained with all extractants for Cu, Pb, and Zn, but not Cd and Ni. The Mehlich 1 soil test was best correlated with total Cu and Zn (r=0.78***, 0.60***, respectively), while the chelate‐based extractants (DTPA and Mehlich 3) were better correlated with total Pb (r=0.85***, 0.63***). Multiple regression equations for the prediction of total Cu, Ni, Pb, and Zn, from soil test extractable metal in combination with easily measured soil properties (pH, organic matter by loss on ignition, soil volume weight) had R² values ranging from 0.41*** to 0.85***, suggesting that it may be possible to monitor, with reasonable success, heavy metal accumulations in soils using the results of a routine soil test.     

Comparison of ammonium bicarbonate‐DTPA,ammonium carbonate,and ammonium oxalate to assess the availability of molybdenum in mine spoils and soils

Abstract

A variety of extractants has been used to assess the availability of molybdenum (Mo) in soils. Most of the extractants have been studied from a deficiency aspect rather than for soils with Mo toxicity, and none of them have been used to extract available Mo from mine spoils. The purpose of this study was to examine the potential of different chemical extractants for assessing the availability of Mo in mine spoils and soils. One mine spoil and three soils were treated with sodium molybdate and then subjected to wetting and drying cycles for two months. These spoil/soils were extracted with ammonium bicarbonate DTPA (AB‐DTPA), ammonium carbonate, and ammonium oxalate solution for available Mo. Crested wheatgrass (Agropyron cristatum) and alfalfa (Medicago sativa) were grown in the spoil/soils in a greenhouse to determine plant uptake of Mo. Additionally, four mine spoils and six soils were extracted and analyzed for available Mo as mentioned above. The results obtained by these three extractants were highly correlated. It was found that ammonium oxalate extracts the greatest amount of Mo among the three extractants from spoil/soils since it dissolves some adsorbed Mo from Fe‐oxide and Al‐oxide. The changes in pH of spoil/soils did not have a significant effect on the amount of Mo extracted by any of these methods. The relationships between Mo uptake and Mo extracted by each method were all significant at 1% level. None of the extractants were clearly better or worse than the others. All three methods can be used to assess Mo availability, and potential toxicity from plant uptake of Mo from reclaimed spoils.     

Combination of Different Extractants to Assess Binding Forms of Some Elements in Soil Profiles

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.     

Comparison of Multi-element to Single‐Element Extractants for Macro‐ and Micronutrients in Acid Soils from Spain

Abstract

Different chemical reagents are used to assess plant‐available nutrients from soils with similar properties. The use of different extractants is a serious limitation when comparing results between different soil‐testing laboratories, often leading to large differences in fertilizer recommendations for similar crops.

In this study, 80 samples from acid soils from Galicia (Spain) were used to compare several soil nutrient extractants. Traditional and tested extractants for acid soil such as Bray 2 and ammonium acetate were used to evaluate multielement extractants such as ethylenediaminetetraacetic acid–ammonium acetate (EDTA‐aa), ammonium bicarbonate–diethylenetriaminepentaacetic acid (AB‐DTPA), and Mehlich 3.

Linear regression analyses were performed to relate the amount of each nutrient obtained by traditional soil extractants to the amount obtained by multielement extractants. Strong correlation was found between extractable Bray 2 P and Mehlich 3 P (r²=0.97, slope=0.87, and intercept=?0.48). The slope of the regression line between EDTA‐aa‐extractable calcium (Ca) and that from ammonium acetate (Aa) approached 1∶1 (r²=0.86). Similar results were obtained for magnesium (Mg) (r²=0.99). Soil zinc (Zn) concentrations extracted by Mehlich 3 and EDTA‐aa were similar; slope of the regression line was 0.95 (r²=0.88). With regard to copper (Cu), Mehlich 3 extracted approximately 20% more Cu than EDTA‐aa.

The results showed that Mehlich 3 and EDTA‐aa are suitable for assessment of plant available phosphorus (P), potassium (K), Ca, Mg, Cu, Zn, and iron (Fe) in acid soils.     

Determination of Appropriate Soil Test Extractant for Available Phosphorus in Southwestern Nigerian Soils

Evaluation of five soil phosphorus (P) extractants was done on southwestern Nigerian soils from sedimentary and basement complex parent materials to determine the relationship between the extractants and the most appropriate extractant for the soils. The soils differed in properties. Generally, soils from the basement material had less available P compared with sedimentary material. Olsen extracted the greatest P. Bray 1 measured 67% of Olsen P, Hunter measured 52%, Mehlich measured 42%, and Ambic measured 24%. Positive and significant regression (P < 0.001) existed among Bray 1, Olsen, Mehlich, Hunter, and Ambic extractants. The strongest relationship was found among Olsen, Mehlich, and Ambic P. The relationship between maize P uptake and extracted P was quadratic, whereas the relationship with Mehlich was logarithmic. Bray, Mehlich, and Olsen P were the significant contributors to the maize P uptake and dry-matter yield. Extractants in order of P extraction were Olsen > Bray 1 > Hunter > Mehlich > Ambic.     

Comparison of extractants for available sludge-borne metals: A residual study

To study the availability of sludge-borne Zn, Cu, Cd, Ni and Pb over time, a field study was conducted. Anaerobically digested sewage sludge (dried on sandbeds) from Huntsville and Chicago were applied to a Decatur silty clay loam soil (clayey, kaolinitic, thermic, Rhodic Paleudult), pH 6.2, for 5 consecutive yr. The sludges were applied at rates of 0, 20 (annual application for 5 yr) and 100 mt ha^?1 (single application). Corn (Zea mays L.) and sudangrass (Sorghum sudanenses) were grown on the sludge-treated plots as test crops in 1987. Plant tissue samples were collected at different growth stages. Soil samples collected from the sludge-treated plots were extracted for Zn, Cu, Cd, Ni and Pb by 0.1 M HCI, DTPA, Mehlich 1 and Mehlich 3 extractants. Statistically, Mehlich 1, Mehlich 3, DTPA and 0.1M HCI extractants all gave highly significant correlations with the plant accumulation of Zn, Cu, Ni and Cd, with DTPA giving the highest at any growth stage for both corn and sudangrass, but they gave poor correlations for Pb. Zinc removed by four extractants was more highly correlated with Zn accumulation by corn (r=0.72^** to 0.93^** p=0.01) and sudangrass (r=0.50^** to 0.96^**, p=0.01) than other metals. Based on higher significant linear correlation coefficients (r), DTPA would be the extractant of choice for both crops; however the advantage to using the Mehlich 3 extractant is that, with a shorter shaking time of 5 min (compared to 2 hr for DTPA), it may be better suited for routine analysis of large numbers of soil samples.

     

Comparison of four extractants and chemical fractions for assessing available zinc and copper in soils of India

Abstract

Relative suitability of different extraction procedures for estimating available zinc (Zn) and copper (Cu) in soils was assessed using DTPA, 0.1 N HCl, ammonium acetate+EDTA, and double acid (HCl+ H₂SO₄) as extractants and rice as a test crop in Neubauer experiment. The relationships between Zn concentration and uptake of Zn by rice plants and Zn extracted by the different methods showed that DTPA‐TEA, pH 7.3, could very suitably be used to assess Zn availability in soils. However, 0.1 N HCl was better for assessing the Cu availability in soils to the rice plants. Water‐soluble and exchangeable fractions of Zn and Cu had significant positive correlations with Zn and Cu concentrations, respectively obtained by all the four extractants tested. The results also showed that DTPA and ammonium acetate+EDTA extracted organically bound Zn, whereas DTPA, 0.1 N HCl and ammonium acetate+EDTA extracted organically bound Cu. Water‐soluble, exchangeable and organic matter bound fractions exhibited significant relationships with Zn and Cu concentrations, their uptake and rice dry matter yield.     

Soil micronutrient contents and relation to other soil properties in Ethiopia

Abstract

Alfisols, Vertisols, Inceptisols, Aridisols, Mollisols, and Entisols were sampled (0–30 cm) from 32 locations across Ethiopia. The soils were analyzed for copper (Cu), zinc (Zn), manganese (Mn), and iron (Fe) contents using 0.005 M diethylene triamine pentaacetic acid (DTPA), 0.05 M hydrochloric acid (HC1), and 0.02 M ethylene diamine tetraacetic acid (EDTA) extractants. EDTA extracted more of each micronutrient than DTPA, which extracted greater amounts than HC1. The quantities of EDTA and DTPA‐extractable micronutrients were significantly correlated, and were in the order: Mn>Fe>Cu>Zn. The order of HCl‐extractable micronutrients was Mn>Fe>Zn>Cu. Micronutrient contents of Mollisols, Vertisols, and Alfisols were usually greater than those of the other soils, and Entisols usually had the lowest micronutrient contents. The contents were mostly positively correlated with clay and Fe₂O₃ contents, but negatively correlated with soil pH and A1₂O₃contents. While comparison of DTPA‐ and EDTA‐extractable micronutrients with critical levels showed that most soils had adequate amounts of the micronutrients for crops, the amounts extracted by HC1 were below critical levels in most soils. Since the critical levels that were used in the comparisons were not established in Ethiopia, calibration of the soil contents of these micronutrients with crops grown in Ethiopia is required to identify the most suitable extractant(s).     

Evaluation of Various Zinc Extractants in Lowland Rice Soil under the Influence of Zinc Sulfate and Chelated Zinc

Field experiments were conducted on rice (cv ‘IET 4094’) in an Aeric endoaquept (pH 7.2) to evaluate the various zinc (Zn) extractants in lowland rice soil under the influence of Zn sulfate and chelated Zn. The diethylenetriaminepentaacetic acid (DTPA), 0.1 N hydrochloric acid (HCl), and 0.05 N HCl‐extractable Zn concentrations in soil increased initially up to the Z29 stage of crop growth when Zn was applied as a single basal source, being greater with Zn ethylenediaminetetraacetic acid (Zn‐EDTA) compared to zinc sulfate (ZnSO₄) application. Among the various extractants, the performance of 0.1 N HCl in extracting Zn was better than the other two extractants and followed the trend 0.1 N HCl > 0.005 M DTPA > 0.05 N HCl. The greatest increase in grain and straw yield of rice was 37.8 and 20.4%, respectively, over the control in the treatment T₇ (1 kg Zn ha^?1 as Zn‐EDTA at basal).     

Mehlich‐1‐ and DTPA‐extractable lead in soils in relation to soil properties

Abstract

Mehlich‐1 and DTPA extractants are frequently used to predict metal availability in soils. Metal extractability by the acid or chelate extractant reflects the metal characteristics and metal‐soil interactions. In this study, samples of eight topsoils from the southeastern United States were incubated with added lead (Pb) at the rate of 40 mg#lbkg^‐1. After five months in the greenhouse, Mehlich‐1 and DTPA extractants were employed to extract Pb in both metal‐amended and natural soils. For the natural soils, Pb concentration in the DTPA extractant was always higher than that in the Mehlich‐1 extractant. This indicates that the DTPA chelate extractant is able to dissolve some Pb in soils which is not solubilized by protons. The negative correlation found between Mehlich‐1‐extractable Pb and soil clay content might result from two mechanisms: i) strong association between Pb and soil surfaces, or ii) readsorption of Pb during extraction. None of the correlations between DTPA‐extractable Pb and soil properties was significant, suggesting that the DTPA‐extractable Pb is not heavily dependent on soil properties. The DTPA extractant showed a high ability to solubilize Pb in the natural soils possibly due to a high affinity of Pb for soil organic matter.     

Influence of residual phosphate fertilizer on labile and extractable zinc in hawaii soils

Abstract

Zinc availability was studied using five soils from Hawaii which had histories of massive phosphorus applications. Heavy phosphate fertilization usually increased extractable Zn, irrespective of the extractant used. The extra extractable Zn associated with the added P probably came from Zn as an accessory element in the fertilizer. Treble superphosphate commonly used in Hawaii contains about 1400 ppm Zn. The Zn content of phosphate fertilizers must be considered before making statements about the effect of fertilizer P on Zn solubility and availability in soils.

Two solutions (0.1N HCl and 0.005M DTPA) were compared as Zn extractants for Hawaii soils. DTPA extracted less Zn than 0.1N HCl. Zinc extracted by repeated HCl treatment was more closely related to the labile Zn pool (E‐values and L‐values) than was DTPA‐extractable Zn. The results suggest that 0.1N HCl extractable Zn, Zn E‐value and Zn L‐value measured the quantity of a single fraction of soil Zn.

Repeated extraction of soil with 0.1N HCl seems to be a suitable procedure for evaluating the Zn status of acid, highly weathered soils of Hawaii.     

Evaluation of universal extractants for determining plant available potassium in intensively cultivated soils

Abstract

Eighteen soils from northwestern Switzerland were used to study the value of seven universal extractants (CaCl₂; DB‐DTPA; Mehlich 1, 2, and 3; Morgan‐Wolf; and NH₄OAc‐EDTA) for predicting plant available potassium (K) as compared to a bioassay (a modified Neubauer test with winter rye). These extractants were evaluated on the basis of K uptake by the bioassay test and the soil K status. In order to create the sufficiency level of exchangeable K for plant growth, soils were treated with 0, 20, 40, 80, and 160 mg K/kg of soil. The range of K uptake by the bioassay tests was between 89.2 and 403.0 mg/kg of soil for the control pots, and 136.6 to 495.8 for the K treatments with optimal conditions for plant growth. The average amounts of K extracted by the seven universal extractants, in ascending order, were: CaCl₂ < Morgan‐Wolf < Mehlich 1 < Mehlich 2 < NH₄OAc‐EDTA < Mehlich 3 < DB‐DTPA. The highest simple correlation with K uptake versus the bioassay test was obtained with the DB‐DTPA (r = 0.89) extractant and the lowest with the Mehlich 1 (r = 0.53) extractant. The DP‐DTPA, NH₄OAc‐EDTA and Mehlich 3‐K procedures showed an advantage over K procedures based on water soluble and exchangeable K pools in the investigated soils in order to predict the amount of plant‐available K. A simple regression and the Cate‐Nelson graphic method offer the possibility of assessing the soil‐K status using K values obtained by these universal extractants and to calibrate them against K forms as follows: exchangeable, water soluble, and non‐exchangeable.     

Evaluation of certain Ni soil tests for an initial estimation of Ni sufficiency critical levels

Although Ni is officially recognized as an essential micronutrient for all higher plants, the majority of the published research on soil availability of Ni focuses on its hazardous role as a heavy metal. The objective of the study was to evaluate certain Ni soil tests in uncontaminated soils for an initial estimation of its sufficiency critical levels. Nickel was extracted from 30 cultivated soils employing the following extraction methods: DTPA, AB‐DTPA, AAAc‐EDTA, Mehlich‐3, 0.1 M HCl, and 0.1 M HNO₃. Ryegrass (Lolium perenne L.) was grown in pots containing the soils, harvested five times, certain plant parameters were determined, and the Cate–Nelson procedures were used for Ni critical levels determination. Among the six methods, HCl was the least reliable extractant for the evaluation of soil available Ni, whereas the most significant (p ≤ 5%) relationships between Ni concentration or Ni uptake by ryegrass and Ni soil tests were consistently obtained for AAAc‐EDTA or Mehlich‐3 extractable Ni. In many cases, > 80% of the variability of Ni concentration or uptake by ryegrass was explained by these two soil tests without the inclusion of other soil properties that affect Ni bioavailability. Sufficiency critical levels of Ni in soil were ≈ 2 mg kg^–1 for both methods. Consequently, as an initial approach, concentrations of AAAc‐EDTA or Mehlich‐3 extractable Ni < 2 mg kg^–1 are probably a good guide to indicate soils that will respond to Ni fertilization.     

Multielement Extraction from Southern Brazilian Soils

To evaluate the effectiveness of multielement extraction of Mehlich 1 and Mehlich 3 solutions in soils from southern Brazil, correlation studies are needed. The amounts of phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), copper (Cu), and zinc (Zn) extracted with Mehlich 1 solution, 1.0 M potassium chloride (KCl), and 0.1 M hydrochloric acid (HCl) for representative soil types of the Rio Grande do Sul state (Brazil) were compared with those extracted with Mehlich 3 solution. The amount of nutrients extracted with different methods indicated high correlation coefficients. On average, Mehlich 3 solution extracted greater amounts of P (50%) and K (20%) than Mehlich 1 solution. Calcium amounts extracted with all solutions were similar. Magnesium amounts extracted with Mehlich 3 solution were on average 20% less than the amounts extracted with 1.0 M KCl solution. Mehlich 3 solution extracted similar amounts of Cu as the 0.1 M HCl but lesser amounts of Zn. Simultaneous multielement soil-test methods such as Mehlich 1 and Mehlich 3 solutions are efficient in soils from southern Brazil and are a feasible alternative to improving the efficiency of soil-testing laboratories.     

不同浸提剂提取的土壤磷铝与油茶各器官磷铝含量的相关分析

采用Mehlich3、ASI、Bray、DTPA、HCl等5种浸提方法测定油茶林地土壤磷、铝含量,并分析其与叶片等器官磷、铝含量的关系。结果表明:ASI法提取的磷含量最高,平均值达4.12 mg/kg,Bray法提取的磷含量最低;铝提取量依次为HCl-AlBray-AlM3-AlASI-AlDTPA-Al。5种方法提取的磷、铝含量分别存在较好的正相关关系。油茶叶片的磷含量和铝含量最高,其中铝含量达14.22 g/kg,是其他器官铝含量的11.5~28.1倍。叶片磷含量与HCl-P、叶片铝含量与HCl-Al分别呈显著正相关。该研究表明0.01 mol/L HCl提取法具有应用于同时测定土壤磷、铝含量和评价其对油茶生物有效性的可行性。