Heavy‐Metal Inhibition of Nitrification in Selected Iowa Soils Treated with Stay‐N 2000

Abstract

Heavy‐metal inhibition of nitrification in soils treated with reformulated nitrapyrin was investigated. Clarion and Okoboji soils were treated with ammonium sulfate [(NH₄)₂SO₄] and a nitrification inhibitor. Copper(II) (Cu), Zinc(II) (Zn), Cadmium(II) (Cd), or Lead(II) (Pb) were added to each soil. A first‐order equation was used to calculate the maximum nitrification rate (K _max), duration of lag period (t′), period of maximum nitrification (Δt), and the termination period of nitrification (t _s). In the Clarion soil, the K _max decreased from 12 mg kg^?1 d^?1 without the nitrification inhibitor to 4, 0.25, 0.86, and 0.27 mg kg^?1 d^?1, respectively, when the inhibitor and Cu, Zn, Pb, or Cd were applied. In the Okoboji soil, K _max decreased from 22 mg kg^?1 d^?1 with no inhibitor to 6, 3, 4, and 2 mg kg^?1 d^?1, respectively, when an inhibitor and Cu, Zn, Pb, or Cd were added. The t′ varied from 8 to 25 d in the Clarion soil and from 5 to 25 d in the Okoboji soil, due to addition of Cu, Zn, Pb, or Cd and the inhibitor.     

The effect of EDTA on the extractability of Zinc (Zn), Cadmium (Cd) and Nickel (Ni) in Vertisol and Alluvial soils

Ethylendiamintetraacetic acid (EDTA) is persistent in the environment. The presence of EDTA in soil may alter the mobility and transport of Zn, Cd and Ni in soils because of the formation of water soluble chelates, thus increasing the potential for metal pollution of natural waters. Mobility of metals is related to their extractability. To investigate metal extractability affected by EDTA, Zn, Cd and Ni were added to Vertisol and Alluvial soil at rates of 50, 2 and 5 mg kg^-1, respectively. Both natural and metal amended soils were treated with Na₂EDTA at rates of 0; 0.2 and 0.5 mg kg^-1. After five months of incubation soil samples were extracted with 0.1 N HCl, 0.005 M DTPA + 0.01 M CaCl₂ + 0.1 M TEA (0.005 M Diethylenetriaminepentaacetic acid + 0.01 M Calcium cloride + 0.1 M Triethanolamine) and 1 M Mg(NO₃)₂, the latter of which extracts the exchangeable from of metald (Zn, Cd and Ni).

According to experiment results, Zn, Cd and Ni in all extraction increased with increasing rates of EDTA in the natural and metal amended soils.     

Determination of Zinc Phytoavailability in Soil by Diffusive Gradients in Thin Films

Assessment of zinc (Zn) phytoavailability by the newly developed technique of diffusive gradients in thin films (DGT) has started gaining more importance because of some advantages over routine soil extractants. A greenhouse study was conducted to determine Zn phytotoxicity thresholds and the phytoavailability of Zn to sorghum sudan (Sorghum vulgare var. sudanese) grass by DGT, compared with calcium chloride (CaCl₂) extraction. Treatments were five Zn levels and two soil pH (6.5 and 6). To obtain various amounts of Zn phytoavailability, soils having two different pH values were amended with zinc sulfate (ZnSO₄) at rates of 0, 150, 300, 600, and 1200 mg Zn kg^?1. Control soil (pH = 6.5) was treated with predetermined elemental sulfur to create different soil pH values (6). Shoot and root Zn concentrations ranged from 27 to 827 mg kg^?1 and 101 to 2858 mg kg^?1, respectively. In general, the Zn concentrations in shoots and roots were increased by increasing Zn concentrations and soil pH. Increasing applied Zn to soil decreased the plant biomass yield and increased adsorption of Zn by DGT. Calcium (Ca) to Zn ratios for all treatments except controls were <26 for shoots and <13 for roots. The CaCl₂‐extractable Zn and effective concentration (C_E) correlated well with plant Zn concentration. A critical shoot Zn concentration for 90% of the control yield was chosen as an indicator of Zn toxicity. The performance of DGT, CaCl₂ extraction, Ca/Zn ratio and plant Zn concentrations were similar for assessing Zn phytoavailability.     

Nitrification in three soils amended with zinc sulfate

Zinc as ZnSO₄ was added to three soils at rates of 0, 10, 100 and 1000 μg Zn g^?1 soil. The soils were uniformly treated with 100 μg Ng^?1 as nh₄cl, incubated at 30°C and NH₄⁺-N and (NO₃^? + NO₂^?)-N determined weekly for 7 weeks. Nitrification in all three soils was totally inhibited by 1000 μg Zn g^?1. At the 100 μg Zn g^?1 rate, nitrification was significantly reduced in two of the three soils during some part of the incubation. This differential effect on nitrification at the 100 μg Zn g^?1 rate was related to differences in soil properties. These results imply that, with respect to nitrification, care should-be taken not to apply Zn-containing materials indiscriminately to soils.     

Mobilization of Cu and Zn in contaminated soil by nitrilotriacetic acid

Batch and upflow column leaching experiments were used to evaluate the nature and extent of Cu and Zn solubilization from contaminated soil by nitrilotriacetic acid (NTA) in 0.025 M NaClO₄. In batch soil suspensions, NTA levels of 10^?5 to 10^?3 M substantially promoted Cu and Zn release from the metal-enriched soil. The ability of NTA to enhance Cu and Zn solubility decreased with increasing solution acidity probably due to competitive binding of NTA by protons and Fe released by hydrous oxide dissolution. However, in the pH range typically encountered in northeastern U.S. soils, soluble metal levels were nearly constant for a given NTA concentration. Leaching soil columns with NTA solutions enhanced Cu release more than Zn, as the enrichment ratio (cumulative metal leached by NTA compared to the 0.025 M NaClO₄ control leachate) after 85 pore volumes displacements was 23.6 and 4.3 for Cu and Zn, respectively. While Cu release by 0.01 M CaCl₂ differed little from the control, 0.01 M CaCl₂ was substantially more effective than 10^?5 M NTA in displacing bound Zn. The data reflect different retention mechanisms for Cu and Zn in this soil.     

Heterotrophic nitrification is the predominant NO3 − production pathway in acid coniferous forest soil in subtropical China

To date, occurrence and stimulation of different nitrification pathways in acidic soils remains unclear. Laboratory incubation experiments, using the acetylene inhibition and ¹⁵N tracing methods, were conducted to study the relative importance of heterotrophic and autotrophic nitrification in two acid soils (arable (AR) and coniferous forest) in subtropical China, and to verify the reliability of the ¹⁵N tracing model. The gross rate of autotrophic nitrification was 2.28 mg?kg^?1?day^?1, while that of the heterotrophic nitrification (0.01 mg?kg^?1?day^?1) was negligible in the AR soil. On the contrary, the gross rate of autotrophic nitrification was very low (0.05 mg?kg^?1?day^?1) and the heterotrophic nitrification (0.98 mg?kg^?1?day^?1) was the predominant NO₃ ^? production pathway accounting for more than 95 % of the total nitrification in the coniferous forest soil. Our results showed that the ¹⁵N tracing model was reliable when used to study soil N transformation in acid subtropical soils.     

长江三角洲地区污水污泥与健康安全风险研究 Ⅲ. 苏、杭二城市污水污泥所施土壤中Cu和Zn的释放动态及其环境风险

未经处理的污泥农业利用后,不仅会增加土壤中污染物的含量,而且会威胁人类和其他生物的健康。室内培养试验结果表明,污泥中的重金属进入土壤后,表现出先释放,后固定的变化趋势,而且随培养时间的增加,施污泥土壤中EDTA和CaCl2提取态Cu和Zn含量逐渐增加,150d时其含量达到最高。与对照处理相比,施污泥土壤中EDTA提取态Cu和Zn含量分别增加了21.4mgkg-1和26.1mgkg-1,而CaCl2提取态Cu和Zn含量分别增加了0.10mgkg-1和3.37mgkg-1。重金属不合格的污泥农业利用存在一定程度的重金属污染风险,且其风险大小与土壤类型、污泥种类和培养时间及污泥的土壤施用量等因素密切相关。选择适宜的土壤类型、污泥种类、施用时间及控制污泥施用量等,能够在一定程度上降低污泥中重金属农业利用的环境风险。     

Zinc Sorption in Sandy Soils from Central Vietnam as a Function of Soil Characteristics

Zinc (Zn) sorption curves were established for 11 cultivated sandy soils from central Vietnam. Soil samples (10 g) were equilibrated with 5 mM calcium chloride (CaCl₂) solutions (50 mL) at five zinc chloride (ZnCl₂) concentrations (0 to 80 mg Zn L^–1). The experimental sorption data were fitted with the Freundlich equation. The amounts of Zn sorbed by soil (Q_Zn) at different Zn concentrations in the equilibrium solution (C_Zn) were closely related to cation exchange capacity (CEC) and pH, that is, to the available exchange sites at given pH values. More specifically, an excellent correlation was found between Zn sorption and exchangeable calcium (Ca_ex), which evidently also depends on CEC and pH. A unique equation was proposed to predict Q_Zn from C_Zn and Ca_ex in the range of Zn loading covered in our research, that is, from traces to Q_Zn ≈ 60 mg Zn kg^–1.     

动力学模型在土壤钾素释放特征描述中的运用及其与化学方法提取的钾素之间的相关性研究

Potassium (K) release characteristics in soil play a significant role in supplying available K. Information on K-release characteristics in soils of central Iran is limited. The objectives of this study were to determine K release characteristics and correlations of K release rate constants with K extracted by different chemical methods in surface soils of ten calcareous soils of central Iran. The kinetics of K release in the soils was determined by successive extraction with 0.01 mol L^-1 CaCl₂ in a period of 2--2 017 h at 25±1 ^oC. Soil K was extracted by distilled water, 0.5 mol L-1 MgNO₃, 0.002 mol L^-1 SrCl₂, 0.1 mol L^-1 BaCl₂, 0.01 mol L^-1 CaCl₂, 1 mol L^-1 NaCl, 1 mol L^-1 boiling HNO₃, 1 mol L^-1 NH₄OAC, Mehlich 1, 0.002 mol L^-1 SrCl₂ 0.05 mol L^-1 citric acid, and ammonium bicarbonate-diethylenetriamine pentaacetic acid (AB-DTPA). A plot of cumulative amounts of K released showed a discontinuity in slope at 168 h. Thus, two equations were applied to two segments of the total reaction time (2--168 and 168--2017 h). Cumulative amounts of K released ranged from 55 to 299 mg kg^-1 in 2--168 h and from 44 to 119 mg kg^-1 in 168--2 017 h. Release kinetics of K in the two time segments conformed fairly well to parabolic diffusion, simplified Elovich, and power function models. There was a wide variation in the K release rate constants. Increasingly higher average concentrations of soil K were extracted by distilled water, Mehlich 1, SrCl₂, CaCl₂, SrCl₂ + citric acid, AB-DTPA, MgNO₃, NaCl, NH₄OAc, BaCl₂ and HNO₃. Potassium release rate constants were significantly correlated with K extracted. The results of this study showed that information obtained from mathematical modeling in two reaction time segments can help to estimate the K-supplying power of soils.     

Evaluation of Extractants and Quantity–Intensity Relationship for Estimation of Available Potassium in Some Calcareous Soils of Western Iran

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.     

Metal Extractability in Binary and Multi-metals Spiked Calcareous Soils

In the present study, a laboratory experiment was designed to compare the 0.01 M calcium chloride (CaCl₂) and diethylenetriaminepentaacetic acid (DTPA) extraction methods for their ability to predict cadmium (Cd), copper (Cu), iron (Fe), Manganese (Mn), nickel (Ni), and zinc (Zn) availability and mobility in five calcareous soils. The soils were spiked with different amounts of metals (0, 50, 100, 200, and 400 mg kg^?1) both in binary (Cu and Zn; Ni and Cd; Fe and Mn) and in multi-systems (Cd, Cu, Fe, Mn, Ni, and Zn) and incubated for 1 months at field capacity. In metal-spiked soils, both extraction methods showed a linear relationship of extractable to total metals for all soils. The fraction of total metals extracted by DTPA was much higher than the fraction extracted by CaCl₂, which was attributed to the formation of soluble metal-complexes in the complexing extracts calculated by the Visual Minteq program. DTPA extraction method showed higher selectivity for Cu over other metals both in binary and in multi-systems. Different order of metals extractability was found in binary and multi-systems for both extraction methods. Solid/solution distribution coefficient (K_d) was calculated by the ratio of the solid phase to soil solution concentration of metals extracted by CaCl₂ or DTPA extraction methods. Both in binary and in multi-systems, the average K_d (l kg^?1) of metals by soils were in the order of Mn (5398) > Fe (4413) > Zn (3376) > Cu (2520) > Ni (969) > Cd (350) in the CaCl₂-extractable metals and Fe (35) ≥ Ni (34) > Zn (18) > Mn (11.2) > Cu (6.3) > Cd (4) in the DTPA-extractable metals. Results showed that among the six studied metals, Cd had the lowest K_d, implying a relative higher mobility in these calcareous soils. The Visual Minteq indicated that in the CaCl₂-extraction method and in both binary and multi-systems the dominant species for Cu, Mn, Ni, and Zn were Cu²⁺, Mn²⁺, Ni²⁺ and Zn²⁺, respectively, while for Cd and Fe, the dominant species were CdCl⁺ and Fe(OH)²⁺, respectively.     

Characterization of phytoavailable zinc in compost-peat substrates — Comparison of methods

Compost of separately collected green yard and organic household wastes may contain high amounts of Zn. Hence, substrates basing on compost can result in Zn phytotoxicity. The aim of the investigations was to identify a suitable reagent to characterize phytoavailable Zn in compost-peat substrates. Petunia hybrids were cultivated in compost-peat substrates with increasing Zn amounts (basic load, 400, 800, 1600 mg kg^?1 d.m. aqua regia soluble). Extractable Zn was determined by extraction of fresh and dried substrates with H₂O, 1 M NH₄NO₃, 0.1 M CaCl₂, 1 M NH₄OAc, and CaCl₂-DTPA (0.01 M + 0.002 M). The Zn content of plants increased significantly with increasing Zn application and decreasing pH. The result of CaCl₂ and NH₄OAc extraction reflected the influence of pH on Zn phytoavailability quite well and the correlation with the plant Zn content was very good. Extraction with H₂O and NH₄NO₃ did not give acceptable results. Extraction with CaCl₂-DTPA was inconsistent for all trials and thus not suitable. The percentage of CaCl₂-extractable Zn in relation to the aqua regia soluble content at the same pH varied over the trials. Thus, the phytoavailable content of the substrates is influenced by additional factors, besides Zn supply and pH. The result of CaCl₂ extraction of dried substrates resulted in the best reflection of Zn phytoavailability and was used for all further investigations, including determination of critical values of phytotoxic Zn. Plant yield was not influenced by the Zn treatments. However, Zn induced chlorosis of petunias occurred at a plant Zn content > 160 mg kg^?1 d.m. and a phytoavailable Zn content in the substrate > 6 mg l^?1 in CaCl₂ extract and > 2.6 mg l^?1 in NH₄OAc extract, respectively.     

Analysis of Proton Generation and Consumption of Forest Surface Soils in Hokkaido, Northern Japan

We determined proton budgets of surface soils in a deciduous forest (Df) and a coniferous forest (Cf) of Volcanogenous Regosols in Tomakomai, Hokkaido of northern Japan. The total H⁺ source was 12.9 and 11.6 kmol_c ha^?1 y^?1 at Df and Cf respectively, and the external H⁺ was 1% at Df and 2% at Cf. The primary H⁺ sources were vegetation uptake of base cations and nitrification, while the major H⁺ sinks were release of base cations and NO₃ ⁺ uptake by vegetation. Leaching incubation experiments using A horizon soils including Df and Cf with NH₄ ⁺ solutions (5.3, 15.9 mg N L^?1) showed that H⁺ from nitrification was generally higher in the Df soil than Cf soil, and nitrification of Tomakomai Df soil was the highest in both treatments. Results of multiple regression analyses suggested that pH_kCl and exchangeable Ca²⁺ contributed to the H⁺ generation via nitrification. Leaching experiments with dilute HCl (pH 3.3) revealed that cation release (mainly Ca²⁺) occurred, and the proportion of release by decrease of exchangeable cations was higher than that by mineral weathering. Mineral weathering in the Tomakomai soil was higher than the other soils.     

Effects of heavy metal accumulation in apple orchard soils on microbial biomass and microbial activities

Abstract

The effects of heavy metals (Cu, Pb, and As) accumulated in apple orchard surface soils on the microbial biomass, dehydrogenase activity, and soil respiration were investigated. The largest concentrations of total Cu, Pb, and As found in the soils used were 1,010, 926, and 166 mg kg^?1 soil, respectively. The amounts of microbial biomass C and N, expressed on a soil organic C and soil total N basis, respectively, were each negatively correlated with the amounts of total, 0.1 M HCI-extractable, and 0.1 M CaCl₂-extractable Cu as logarithmic functions, the correlation coefficient being lowest for the 0.1 M CaCl₂extractable Cu. Nevertheless, they were not correlated with the soil pH which was controlling the solubility of Cu in 0.1 M CaCl₂. The dehydrogenase activity expressed per unit of soil organic C was also negatively correlated with the amounts of total, 0.1 M HCI-extractable Cu, and 0.1 M CaCl₂-extractable Cu as logarithmic functions. However, the correlation coefficient was highest for the 0.1 M CaCl₂-extractable Cu. Although the soil respiration per unit of soil total organic C did not show any significant correlations with the total concentrations of heavy metals, it showed negative significant correlations with the amount of 0.1 M HCI-extractable Cu, and to a greater extent, with the amount of 0.1 M CaCl₂-extractable Cu. Both the dehydrogenase activity and respiration per unit of soil total organic C increased significantly with increasing soil pH. These results suggested that in apple orchard soils with heavy metal accumulation the microbial biomass was adversely affected by the slightly soluble Cu, whereas the microbial activities by the readily soluble Cu whose amount depended on the soil pH. The respiration per unit of microbial biomass C showed a positive significant correlation with the logarithmic concentration of total Cu. Furthermore, the contribution of fungi to substrate-induced respiration increased with increasing total Cu content in the soils.     

Use of reactive phosphate rocks as fertilizer on acid upland soils in Indonesia: accumulation of cadmium and zinc in soils and shoots of maize plants

A pot experiment was conducted to study the contribution of reactive phosphate rocks (RPRs) on the accumulation of Cd and Zn in 10 acid upland soils in Indonesia and shoots of Zea mays plants grown on these soils. Two types of RPR were used at a rate of 0.5 g (kg soil)^–1: RPRL containing 4 mg Cd kg^–1 and 224 mg Zn kg^–1, and RPRH containing 69 mg Cd kg^–1 and 745 mg Zn kg^–1. Zea mays was harvested at 6 weeks after planting. The application of RPRH significantly increased the concentrations of Cd in the shoots. The application of this RPR also increased the amount of Cd which could be extracted by 0.5 M NH₄‐acetate + 0.02 M EDTA pH 4.65 from the soils. More than 90% of the added Cd remained in the soil. As Zn is an essential element and the studied acid upland soils are Zn‐deficient, increased plant growth upon RPR application might be partly attributed to Zn present in the phosphate rock. However, more experiments are needed to confirm this hypothesis. The Cd and Zn concentrations and CEC of the soils were important soil factors influencing the concentrations of Cd and Zn in the shoots of maize plants grown on these soils.     

Zinc toxicity on N2O reduction declines with time in laboratory spiked soils and is undetectable in field contaminated soils

Denitrification assays in soils spiked with zinc salt have shown inhibition of the N₂O reduction resulting in increased soil N₂O fluxes with increasing soil Zn concentration. It is unclear if the same is true for environmentally contaminated soils. Net production of N₂O and N₂ was monitored during anaerobic incubations (25 °C, He atmosphere) of soils freshly spiked with ZnCl₂ and of corresponding soils that were gradually enriched with metals (mainly Zn) in the field by previous sludge amendments or by corrosion of galvanized structures. Total denitrification activity (i.e. the sum of N₂O+N₂ production rate) was not inhibited by freshly added Zn salts up to 1600 mg Zn kg⁻¹, whereas N₂O reduction decreased by 50% (EC₅₀) at total Zn concentrations of 231 mg Zn kg⁻¹ (ZEV soil) and 368 mg Zn kg⁻¹ (TM soil). In contrast, N₂O reduction was not reduced by soil Zn in any of the field contaminated soils, even at total soil Zn or soil solution Zn concentrations exceeding more than 5 times corresponding EC₅₀'s of the freshly spiked soil. The absence of adverse effects in the field contaminated soils was unrelated to soil NO₃ or organic matter concentration. Ageing (2-8 weeks) and soil leaching after spiking reduced the toxicity of Zn on N₂O reduction, either expressed as total Zn or soil solution Zn, suggesting adaptation reactions. However, no full recovery after spiking was identified at the largest incubation period in one soil. In addition, the denitrification assay performed with sewage sludge showed elevated N₂O release in Zn contaminated sludges (>6000 mg Zn kg⁻¹ dry matter) whereas this was not observed in low Zn sludge (<1000 mg Zn kg⁻¹ dry matter) suggesting limits to adaptation reactions in the sludge particles. It is concluded that the use of soils spiked with Zn salts overestimates effects on N₂O reduction. Field data on N₂O fluxes in sludge amended soils are required to identify if metals indeed promote N₂O emissions in sludge amended soils.     

Decomposition rate of dicyandiamide and nitrification inhibition

Abstract

Degradation of dicyandiamide (DCD) was assayed in laboratory studies at 8, 15, and 22 C in a Decatur silt loam and in a Norfolk loamy sand. Dicyandiamide was very short lived at 22 C, with half‐lives of 7.4 and 14.7 days in the Decatur and Norfolk soils, respectively. In the Norfolk soil at 8 C, half‐life increased to 52.2 days. In a nitrificaton study of both soils at 22 C, 80 mg (NH₄)₂SO₄‐N kg^‐1 of soil was applied with 20 mg DCD‐N kg^‐1 of soil and 100 mg kg^‐1 (NH₄)₂S0₄‐N was added with 5% nitrapyrin. Distinct lag phases preceded zero order nitrification with the inhibitor treatments. Lag periods were 2 and 2.6 times the half life of DCD in the degradation study for Decatur and Norfolk soils, respectively. Like most nitrification inhibitors, the effectiveness of DCD decreases with increasing temperature. In the Norfolk loamy sand, nitrification inhibition by DCD was equal to nitrapyrin for up to 42 days, but in Decatur silt loam, DCD was less potent to nitrapyrin as a nitrification inhibitor.     

The Effects of Copper and Lead on Growth and Zinc Accumulation of Thlaspi Caerulescens J. and C. Presl: Implications for Phytoremediation of Contaminated Soils

Thlaspi caerulescens J. and C. Presl is a Zn-hyperaccumulatingplant which has aroused considerable interest with respect to its possible use for phytoremediation of Zn-contaminated soils. In this work, a British population of T. caerulescens, from a soil which was found to have relatively high concentrations of water-extractable Cu (0.22 mg L^-1), Pb (0.99 mg L^-1) and Zn (6.49 mg L^-1), was studied. Its ability to grow and accumulate Zn from hydroponic nutrient solution in the presence of elevated concentrations of Cu and/or Pb was investigated. The chosen concentrations of Cu, Pb and Zn were based on reported water-soluble concentrations of these heavy metals in contaminated soils. When supplied with 32.7 mg L^-1 Zn, plants accumulated 19 780 mg kg^-1 Zn in their shoot dry matter. This concentration declined by 9.3, 87 and 84% respectively when 5.0 mg L^-1 Pb, 1.0 mg L^-1 Cu or 2.0 mg L^-1 Cu were included in the nutrient solution. Despite the apparent adaptation of this population of T. caerulescens to a Zn/Pb/Cu-contaminated soil, these Cu treatments strongly inhibited growth, but the Pb treatment did not affect growth significantly.     

不同磷源对设施菜田土壤速效磷及其淋溶阈值的影响

土壤中磷的移动性不仅取决于磷的数量且与磷肥形态有关。了解不同磷源（有机肥和化肥）对设施菜田土壤磷素的影响对于指导科学施肥和面源污染防治至关重要。本文选取河北省饶阳县3种不同磷含量的农田土壤（未种植过蔬菜的土壤、种植蔬菜30年的塑料大棚土壤和种植蔬菜4年的日光温室土壤）为研究对象,采用室内培养试验和数学模型模拟方法研究有机无机磷源对设施菜田土壤磷素的影响,确定无机肥和有机肥源土壤磷素淋溶的环境阈值。结果表明添加有机肥和无机磷肥都会显著增加3种不同种植年限设施菜田土壤速效磷（Olsen-P）和氯化钙磷（CaCl₂-P）含量,但增加速度不同。对于未种植过蔬菜的低磷对照土壤,磷投入量高于50 mg·kg^-1（干土）后,无机肥比有机肥显著提高了土壤Olsen-P含量。对于已种植蔬菜30年的塑料大棚土壤,高磷投入时[300 mg·kg^-1（干土）和600 mg·kg^-1（干土）],无机肥比有机肥显著提高了土壤Olsen-P含量,低于此磷投入量时有机肥和无机肥处理之间没有显著差异。3种不同农田土壤CaCl₂-P的含量所有处理均表现出无机肥显著高于有机肥处理,尤其是在高磷量[>300 mg·kg^-1（干土）]投入时表现更加明显。两段式线性模拟结果表明,设施菜田土壤有机肥源磷素和无机肥源磷素淋溶阈值分别为87.8 mg·kg^-1和198.7 mg·kg^-1。随着土壤Olsen-P的增加,添加无机肥源磷对设施菜田土壤CaCl₂-P含量的增加速率是有机肥源磷的两倍。因此,建议在河北省高磷设施菜田应减少无机磷肥的投入,特别是土壤速效磷高于198.7 mg·kg^-1的设施菜田应禁止使用化学磷肥和有机肥,在土壤速效磷低于198.7 mg·kg^-1的设施菜田应加大有机肥适度替代无机肥技术的推广。     

Applicability of 0.01 M CaCl2 as a single extraction solution for the assessment of the nutrient status of soils and other diagnostic purposes

Abstract

The applicability of 0.01 M CaCl₂ solution as a single extraction agent for soils as a basis for fertilizer recommendation was tested on a variety of soils both from the Netherlands and from some tropical countries. Air‐dry soil samples were subjected to extraction with 0.01 M CaCl₂ and to several conventional extraction procedures, and the results were compared. In the soil suspensions pH was measured, whereas in the extracts Na, K, Mg, P, different extractable N‐forms and Zn were measured. The values found in CaCl₂ extracts are discussed in relation to results of other extraction procedures and as to their potential value in soil quality assessment. It is concluded that a single extraction procedure with 0.01 M CaCl₂ can be applied for fertilizer recommendation purposes. The possibility of determining different extractable N‐forms (NH₄, NO₃, soluble organic N) significantly enhances the value of the method in predicting the N‐fertilizer needs. Furthermore it was found that the concentration of Zn in 0.01 M CaCl₂ extracts was a good indicator of phytotoxicity in a polluted area. Additional advantages of this extraction are low costs, simplicity and repro‐ducibility.