Effects of Soil Amended with Cadmium and Lead on Growth,Yield, and Metal Accumulation and Distribution in Parsley

A greenhouse experiment was designed to determine the cadmium (Cd) and lead (Pb) distribution and accumulation in parsley plants grown on soil amended with Cd and Pb. The soil was amended with 0, 5, 10 20, 40, 60, 80, and 100 mg Cd kg^?1 in the form of cadmium nitrate [Cd(NO₃)₂] and 0, 5, 10, 50 and 100 mg Pb kg^?1 in the form of lead nitrate [Pb(NO₃)₂]. The main soil properties; concentrations of the diethylenetriaminepentaacetic acid (DTPA)–extractable metals lead (Pb), Cd, copper (Cu), iron (Fe), zinc (Zn), and manganese (Mn) in soil; plant growth; and total contents of metals in shoots and roots were measured. The DTPA-extractable Cd was increased significantly by the addition of Cd. Despite the fact that Pb was not applied, its availability was significantly greater in treatments 40–100 mg Cd kg^?1 compared with the control. Fresh biomass was increased significantly in treatments of 5 and 10 mg Cd kg^?1 as compared to the control. Further addition of Cd reduced fresh weight but not significantly, although Cd concentration in shoots reached 26.5 mg kg^?1. Although Pb was not applied with Cd, its concentration in parsley increased significantly in treatments with 60, 80, and 100 mg Cd g^?1 compared with the others. Available soil Pb was increased significantly with Pb levels; nevertheless, the increase was small compared to the additions of Pb to soil. There were no significant differences in shoot and root fresh weights between treatments, although metal contents reached 20.0 mg Pb kg^?1 and 16.4 mg Pb kg^?1 respectively. Lead accumulation was enhanced by Pb treatments, but the positive effect on its uptake was not relative to the increase of Pb rates. Cadmium was not applied, and yet considerable uptake of Cd by control plants was evident. The interactive effects of Pb and Cd on their availability in soil and plants and their relation to other metals are also discussed.     

Controlled‐release urea decreased ammonia volatilization and increased nitrogen use efficiency of cotton

Excessive nitrogen (N) fertilizer input leads to higher N loss via ammonia (NH₃) volatilization. Controlled‐release urea (CRU) was expected to reduce emission losses of N. An incubation and a plant growth experiment with Gossypium hirsutum L. were conducted with urea and CRU (a fertilizer mixture of polymer‐coating sulfur‐coated urea and polymer‐coated urea with N ratios of 5 : 5) under six levels of N fertilization rates, which were 0% (0 mg N kg⁻¹ soil), 50% (110 mg N kg⁻¹ soil), 75% (165 mg N kg⁻¹ soil), 100% (220 mg N kg⁻¹ soil), 125% (275 mg N kg⁻¹ soil), and 150% (330 mg N kg⁻¹ soil) of the recommended N fertilizer rate. For each type of N fertilizer, the NH₃ volatilization, cotton yield, and N uptake increased with the rate of N application, while N use efficiency reached a threshold and decreased when N application rates of urea and CRU exceeded 238.7 and 209.3 mg N kg⁻¹ soil, respectively. Ammonia volatilization was reduced by 65–105% with CRU in comparison to urea treatments. The N release characteristic of CRU corresponded well to the N requirements of cotton growth. Soil inorganic N contents, leaf SPAD values, and net photosynthetic rates were increased by CRU application, particularly from the full bloom stage to the initial boll‐opening stage. As a result, CRU treatments achieved significantly higher lint yield by 7–30%, and the N use efficiency of CRU treatments was increased by 25–124% relative to that of urea treatments. These results suggest that the application of CRU could be widely used for cotton production with higher N use efficiency and lower NH₃ volatilization.     

Role of soil constituents in fixation of soluble Zn, Cu, Ni and Cd added to soils

Slow immobilization of trace metals in soil, termed ‘fixation’, affects their natural attenuation but it is still unclear which reactions occur. Twenty‐eight soils were selected to assess the role of Fe oxides and carbonates on fixation of Cu, Cd, Zn and Ni. Soils included samples from 2 toposequences (Vietnam, Spain) and 13 European topsoils with different soil characteristics (pH 3.4–7.7). Samples were amended with 250 mg Zn kg⁻¹, 100 mg Cu kg⁻¹, 80 mg Ni kg⁻¹ and 2.5 mg Cd kg⁻¹ as metal salts and incubated for 850 days. Fixation was measured as the increase of the fraction of added metals that were not isotopically exchangeable. Fixation increased with time and was, averaged over all the soils, 43% (Cu), 41% (Zn), 41% (Ni) and 28% (Cd) after 850 days. Metal fixation within samples from each toposequence was generally positively related to total Fe oxide concentration (Fe_d) for Zn, Ni and Cd. However, the fixation of Cd, Zn and Ni was mainly explained by pH and not by Fe_d when considering all soils. Fixation of Zn and Cd in soils with pH >7.0 increased with increasing concentrations of carbonates at initial ageing times. Fixed fractions of Zn, Ni and Cd were significantly released when experimentally removing 50% of carbonates by acidification. Fixation of Cu was most poorly related to soil properties. Our data suggest that fixation of Cd, Zn and Ni is related to a pH‐dependent diffusion into oxides and that of Cd and Zn also to diffusion and/or coprecipitation in carbonates. Fixation of Ni at neutral pH may also be related to stabilization of precipitates that form readily in soil.     

Plant uptake of metals,transfer factors and prediction model for two contaminated regions of Kosovo

The bioavailability and plant uptake of heavy metals (HM), as well as finding the most reliable methods for the prediction of availability, continues to be one of the most crucial problems in agricultural and environmental studies. In agricultural soils from two regions in Kosovo, known for its metal pollution, we collected 60 soil and plant samples (wheat, corn, potatoes, and grass). Heavy metals were extracted from soil with aqua regia (pseudototal concentration), NH₄OAc‐EDTA (potential bioavailable), and NH₄NO₃ (mobile fraction), plant samples were digested with HNO₃/H₂O₂ (microwave assisted extraction). The pseudo total content of Cd, Pb, and Zn showed high value in Mitrovice (mean: Cd–2.92, Pb–570.15, and Zn–522.86 mg kg^?1), whereas in Drenas region Ni and Cr showed high value with a mean 258.54 and 203.22 mg kg^?1. Also, the potential bioavailability and mobile form of these metals were increased in Mitrovice (mean: Cd–1.59, Pb–217.05, Zn–522.86 mg kg^?1, respectively Cd–0.17, Pb–0.64, and Zn–15.45 mg kg^?1), compared to Drenas. Cd and Pb were elevated in potato tubers (mean Cd–0.48 and Pb–0.85 mg kg^?1). The TF was higher for micronutrients (Zn and Cu) than for non‐essential metals (Cd and Pb). Multiple regression analysis showed a good model for prediction of Cd, Pb and Zn content in plant with significance 99.9%, whereas this model was not significant for Cu, Cr, and Ni. Soil pH played a significant role in the content of Cd and Zn in wheat and potato plants. Clay content also showed significance in Cd concentration in wheat and potato plants, while carbon content was significant for Cd in grass plants, as well as for Zn in wheat and grass plants.     

Immobilization of heavy metals in soils using inorganic amendments in a greenhouse study

The effect of red mud (10 g kg^–1), a by‐product of the alumina industry, zeolite (20 g kg^–1), a naturally‐occurring hydrous aluminosilicate, and lime (3 g kg^–1) on metal lability in soil and uptake by fescue (Festuca rubra L.) (FEST) and amaranthus (Amaranthus hybridus L.) (AMA) was investigated in four different soils from Austria. The soil collection locations were Untertiefenbach (UNT), Weyersdorf (WEY), Reisenberg (REI), and Arnoldstein (ARN). The latter was collected in the vicinity of a former Pb‐Zn smelter and was highly polluted with Pb (12300 mg kg^–1), Zn (2713 mg kg^–1), and Cd (19.7 mg kg^–1) by long‐term deposition. The other soils were spiked with Zn (700 mg kg^–1), Cu (250 mg kg^–1), Ni (100 mg kg^–1), V (100 mg kg^–1), and Cd (7 mg kg^–1) salts in 1987. The two plant species were cultivated for 15 months. Ammonium nitrate (1 M) extraction was used in a soil : solution ratio of 1:2.5 to assess the influence of the amendments on the labile metal pools. The reduction of metal extractability due to red mud was 70 % (Cd), 89 % (Zn), and 74 % (Ni) in the sandy soil (WEY). Plant uptake in this treatment was reduced by 38 to 87 % (Cd), 50 to 81 % (Zn), and 66 to 87 % (Ni) when compared to the control. Sequential extraction revealed relative enrichments of Fe‐oxide‐associated metal fractions at the expense of exchangeable metal fractions. Red mud was the only amendment that decreased lability in soil and plant uptake of Zn, Cd, and Ni consistently. Possible drawbacks of red mud application (e.g., As and Cr concentration) remain to be evaluated.     

Lead and Cadmium in Soils of La Rioja Vineyards,Spain

Land degradation can be triggered by the abuse of chemicals that damage soil quality. Agriculture is changing the chemical and physical properties of soils, and in vineyards, those changes are due to the use of pesticides. In order to assess the Pb and Cd content, 212 soil samples from La Rioja D.O.Ca were analysed. Concentrations of Pb in soil ranged from 0·96 to 64·31 mg kg⁻¹ with a mean concentration of 21·26 mg kg⁻¹ in the surface layer, while they ranged from 7·97–43·93 mg kg⁻¹ with a mean of 20·83 mg kg⁻¹ in the subsurface layer. The mean content of bioavailable lead was 1·03 mg kg⁻¹ in the surface layer and 0·76 mg kg⁻¹ in the subsurface. Cd overall average concentration was 0·29 mg kg⁻¹ in the surface; in the subsurface, the mean was 0·31 mg kg⁻¹ and ranged from 0·10 to 1·22 mg kg⁻¹. The values in the surface layers were 0·15 mg kg⁻¹ and in the subsurface layer 0·01 of Cd bioavailability. On the basis of pedogeochemical Pb and Cd distribution, balanced fertilization will be of great importance for sustainable development of agricultural wine‐producers. Copyright © 2016 John Wiley & Sons, Ltd.     

Predicting heavy metal transfer from soil to plant: potential use of Freundlich‐type functions

Soil‐plant transfer of metals is a nonlinear process. We therefore aimed at evaluating the potential of Freundlich‐type functions (c_Plant = b × c_Soil^a) to predict Cd, Cu, Pb, and Zn concentrations in wheat (Triticum aestivum L.) grain and leaf (c_Plant) from soil concentrations (c_Soil). Wheat plants and soil A horizons, mainly developed from Holocene sediments, were sampled at 54 agricultural sites in Slovakia. Metals were extracted from soils with 0.025 M EDTA at pH 4.6 and concentrated HNO₃/HClO₄ (3:1); plant samples were digested with concentrated HNO₃. Total metal concentrations of soil samples were 0.07—25 mg Cd kg^—1, 9.3—220 mg Cu kg^—1, 14—1827 mg Pb kg^—1, and 34—1454 mg Zn kg^—1. On average, between 20 % (Zn) and 80 % (Cd) of the total concentrations were EDTA‐extractable. The total metal concentrations of grain samples were < 0.01—1.3 mg Cd kg^—1, 1.3—6.6 mg Cu kg^—1, < 0.05—0.30 mg Pb kg^—1, and 8—104 mg Zn kg^—1. The leaves contained up to 3.2 mg Cd kg^—1, 111 mg Cu kg^—1, 4.3 mg Pb kg^—1, and 177 mg Zn kg^—1. Linear regression without data transformation was precluded because of the nonnormal data distribution. The Freundlich‐type function was suitable to predict Cd (grain: r = 0.71, leaf: 0.86 for the log‐transformed data) and Zn concentrations (grain: 0.69, leaf: 0.68) in wheat grain and leaf from the EDTA‐extractable metal concentrations. The prediction of Cu and Pb concentrations in grain (Cu: r = 0.44, Pb: 0.41) was poorer and in leaf only possible for Pb (0.50). We suggest to use the Freundlich‐type function for defining threshold values instead of linear regression because it is more appropriate to simulate the nonlinear uptake processes and because it offers interpretation potential. The results suggest that the coefficient b of the Freundlich‐type function depends on the intensity of metal uptake, while the coefficient a reflects the plants' capability to control the heavy metal uptake. The latter is also sensitive to metal translocation in plants and atmospheric deposition.<?show $6#>     

Importance of heterotrophic nitrification and dissimilatory nitrate reduction to ammonium in a cropland soil: Evidences from a 15N tracing study to literature synthesis

Future climate change is predicted to influence soil moisture regime, a key factor regulating soil nitrogen (N) cycling. To elucidate how soil moisture affects gross N transformation in a cultivated black soil, a ¹⁵N tracing study was conducted at 30%, 50% and 70% water-filled pore space (WFPS). While gross mineralization rate of recalcitrant organic N (N_rec) increased from 0.56 to 2.47 mg N kg⁻¹ d⁻¹, the rate of labile organic N mineralization declined from 4.23 to 2.41 mg N kg⁻¹ d⁻¹ with a WFPS increase from 30% to 70%. Similar to total mineralization, no distinct moisture effect was found on total immobilization of ammonium, which primarily entered the N_rec pool. Nitrate (NO₃⁻) was mainly produced via autotrophic nitrification, which was significantly stimulated by increasing WFPS. Unexpectedly, heterotrophic nitrification was observed, with the highest rate of 1.06 mg N kg⁻¹ d⁻¹ at 30% WFPS, contributing 31.8% to total NO₃⁻ production, and decreased with WFPS. Dissimilatory nitrate reduction to ammonium (DNRA) increased from near zero (30% WFPS) to 0.26 mg N kg⁻¹ d⁻¹ (70% WFPS), amounting to 16.7–92.9% of NO₃⁻ consumption. A literature synthetic analysis from global multiple ecosystems showed that the rates of heterotrophic nitrification and DNRA in test soil were comparative to the forest and grassland ecosystems, and that heterotrophic nitrification was positively correlated with precipitation, soil organic carbon (SOC) and C/N, but negatively with pH and bulk density, while DNRA showed positive relationships with precipitation, clay, SOC, C/NO₃⁻ and WFPS. We suggested that low pH and bulk density and high SOC and C/N in test soil might favor heterotrophic nitrification, and that C and NO₃⁻ availability together with anaerobic condition were crucial for DNRA. Overall, our study highlights the role of moisture in regulating gross N turnover and the importance of heterotrophic nitrification for NO₃⁻ production under low moisture and DNRA for NO₃⁻ retention under high moisture in cropland.     

Effects of Phosphorus Additions on Lead,Cadmium, and Zinc Bioavailabilities in a Metal-Contaminated Soil

The use of phosphorus (P) to reduce lead (Pb)bioavailability is being proposed as an alternative to excavationand disposal as a remedial technology for Pb-contaminated soilsin residential areas. The objective of this study was todetermine the influence of P sources and rates andCaCO₃additions on the bioavailabilities of Pb, cadmium (Cd), and zinc(Zn) in a contaminated soil material using plants, a sequentialextraction procedure, and ion activities in equilibrium solutionas indicators. A contaminated soil containing 370 mg kg^-1 Cd, 2800 mg kg^-1 Pb and 29100 mg kg^-1 Zn was amended ina factorial arrangement of CaCO₃ (0 or 2000 mg kg^-1) and P as rock phosphate or KH₂PO₄ at 0:1, 2:1 or 4:1P:Pb mole ratios. A pot study was conducted using sorghum-sudangrass (Sorghum bicolor L. Moench). The addition of P did not influence Pb concentrations in plant tissue and had little effect on Cd concentrations. An interaction between P source and level of P addition was found for Zn concentrations in plant tissue; concentrations increased with increasing amounts of P from KH₂PO₄ anddecreased with increasing amounts of P from rock phosphate. Sequential extraction results suggested a much greater reduction in Pb bioavailability from treatment withKH₂PO₄ than with rock phosphate and that P influencedthe fractionations of Cd and Zn. Activities of Cd²⁺,Pb²⁺, and Zn²⁺ in equilibrium solutions generally weredecreased by rock phosphate and increased by KH₂PO₄. Saturation indices suggested the addition ofKH₂PO₄shifted the soil equilibrium from octavite to hydroxypyromorphite, whereas solid-phase control of Cd²⁺ andZn²⁺ was not influenced by soil amendments. A soluble Psource was more effective in reducing Pb bioavailability thanrock phosphate but had variable effects on Cd and Znbioavailabilities.     

Roles of Bacillus megaterium in Remediation of Boron,Lead, and Cadmium from Contaminated Soil

Phytoremediation is an attractive, economical alternative to soil removal and burial methods to remediate contaminated soil. The objective of this study was to investigate the effects of adding different rates of Bacillus megaterium on the capacity of Brassica napus plants to take up boron (B), lead (Pb), and cadmium (Cd) from polluted soils under field conditions. Field experiments were conducted using a randomized complete block design with control (without pollution and B. megaterium application) and B, Pb, and Cd in two doses (0 and 100 mg kg^?1), B. megaterium with four doses (no application and 10⁸ cfu B. megaterium ml^?1 sprayed at 50 ml plot^?1, 100 ml plot^?1, 150 ml plot^?1). Results indicated that soil pollution treatments significantly decreased seed (SDMY), shoot (SHDMY), root (RDMY), and total dry-matter yield (TDMY) of plants at 42.9, 3.8, 62.6, and 23.4% for B-polluted treatment; 25.8, 8.7, 17.6, and 14.2% for Pb-polluted treatment; and 33.2, 7.0, 14.0, and 16.4% for Cd-treatment without B. megaterium application, respectively. However, the application of B. megaterium ameliorated the negative effects of B, Pb, and Cd at 41.4, 52.7, and 10.9% for B; 24.4, 21.6, and 4.9% for Pb; and 22.8, 22.0, and 3.3% for Cd, respectively. The potentially bioavailable and relatively available fraction of soil B, Pb, and Cd increased with increases in the B. megaterium application but total fraction and stable fraction decreased. It is concluded that the seed and shoot parts of B. napus can be used as hyperaccumulators for plant B, Pb, and Cd remediation according to remediation factors but the shoot is the biggest part of the plant, and thus an important portion of the plant to remove B, Pb, and Cd from the B-, Pb-, and Cd-contaminated soils. To decrease desired concentration for 8 mg B kg^?1, 4 mg Pb kg^?1, and 3 mg Cd kg^?1 in the active rooting zone of soil, approximately 2, 6, and 21 years would be necessary with only 150 ml plot^?1 B. megaterium–sprayed soil cultivated with B. napus, respectively.     

氮肥对镉在土壤-芥菜系统中迁移转化的影响

以芥菜为研究对象, 采用盆栽试验, 探讨了不同用量的5种氮肥对污染农田土壤中镉(Cd)在土壤–根系–地上部迁移累积的影响。结果表明: 5种氮肥均促进了芥菜根系对Cd的吸收, 且根系Cd含量随施氮量的增加而增加; 但根系吸收转运Cd的能力随氮肥施用量的增加呈先降后增的变化趋势。在≤200 mg(N)·kg^-1(土)的施氮水平下, CO(NH₂)₂和Ca(NO₃)₂处理能显著降低芥菜地上部Cd含量, 降低幅度分别为13%~29%和24%~30%。在施氮量相同的条件下, NH₄Cl和(NH₄)₂SO₄显著降低了土壤pH, 增加了土壤DTPA-Cd含量, 促进了芥菜对Cd的吸收。本试验条件下, 200 mg(N)·kg^-1(土)的CO(NH₂)₂在增加芥菜产量和降低芥菜地上部Cd含量等方面优于其他氮肥处理。     

Chelate-Assisted Phytoextraction of Cadmium and Lead using Mustard and Fenugreek

A screen-house experiment was conducted to study cadmium (Cd) and lead (Pb) phytoextraction using mustard and fenugreek as test crops. Cadmium was applied at a rate of 20 mg kg^?1 soil for both crops, and Pb was applied at 160 and 80 mg kg^?1 soil for mustard and fenugreek, respectively. The disodium salt of ethylenediamine tetraacetic acid (EDTA) was applied at 0, 0.5, 1.0, and 1.5 g kg^?1 soil. Dry-matter yield (DMY) of both crops decreased with increasing rates of EDTA application. Application of 1.5 g EDTA kg^?1 soil caused 23% and 70% declines in DMY of mustard and fenugreek shoots, respectively, in the soils receiving 20 mg Cd kg^?1 soil. Similarly, in soil with 160 mg Pb kg^?1 soil, application of 1.5 g EDTA kg^?1 resulted in 25.4% decrease in DMY of mustard shoot, whereas this decrease was 55.4% in fenugreek grown on a soil that had received 80 mg Pb kg^?1 soil. The EDTA application increased the plant Cd and Pb concentrations as well as shoot/root ratios of these metals in both the crops. Application of 1.5 g kg^?1 EDTA resulted in a 1.50-fold increase in Cd accumulation and a 3-fold increase in Pb accumulation by mustard compared to the control treatment. EDTA application caused mobilization of Cd and Pb from carbonate, manganese oxide, and amorphous iron oxide fractions, which was evident from decrease in these fractions in the presence of EDTA as compared to the control treatment (no EDTA).     

Assessment of soil contamination by potentially toxic elements in the aljustrel mining area in order to implement soil reclamation strategies

Land pollution due to past mining activities is a major environmental issue in many European countries. The Aljustrel mine (SW Portugal), located in the western sector of the Iberian Pyrite Belt (IBP) presents a negative visual and environmental impact as a consequence of the mining activity that has developed since the Roman era. Its impacts are also a restraint on the life quality of the population. The exposure of pyrite and other sulphides to air are responsible for the pollution observed in soils, surface water and stream sediments. This paper investigates the pollution load of potential toxic elements in soil samples collected around the Aljustrel mining area. The aim is to assess the levels of soil contamination with respect to average concentrations of toxic elements in the region and to understand the partitioning and availability of pollutants in the area. The results showed severe soil contamination (mainly As, Cd, Cu, Pb and Zn). The concentrations of As (up to 3936 mg kg⁻¹) and certain heavy metals (up to 5414 mg kg⁻¹ Cu, 61·6 mg kg⁻¹ Cd, 20 000 mg kg⁻¹ Pb and 20 000 mg kg⁻¹ Zn) are two orders of magnitude above the regional South Portuguese Zone (SPZ) background values. The median concentrations of As, Cd, Cu, Pb and Zn exceed the values established for world soils, the European Union, Portugal and Andalusia. The results suggest that the distribution patterns of Co, Cr and Ni element concentrations in the Aljustrel area are primarily influenced by the lithology and geochemistry nature of bedrock. The soil background of this geological domain is characterized by relatively high heavy metal contents, essentially derived from the parent rocks. Copyright © 2010 John Wiley & Sons, Ltd.     

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.     

Spatiotemporal Heterogeneity of Soil Available Nitrogen During Crop Growth Stages on Mollisol Slopes of Northeast China

Spatiotemporal heterogeneity of soil available nitrogen (AN) (sum of NO₃⁻–N and NH₄⁺–N) is the essential basis for soil management and highly correlates to crop yield. Both geostatistical and traditional analyses were used to describe the spatiotemporal distribution of AN in the 0–20‐cm soil depth on typical Mollisol slopes (S1 and S2) in Northeast China. The concentration of NO₃⁻–N dynamics at slope positions was typically opposite to NH₄⁺–N. The peak values of AN typically moved from the summit of the slope to the bottom from spring to autumn and were mainly influenced by the content of NO₃⁻–N (S1, 7·9–18·9 mg kg⁻¹; S2, 1·2–103·6 mg kg⁻¹), both of NO₃⁻–N (S1, 3·9–8·3 mg kg⁻¹; S2, 2·2–28·0 mg kg⁻¹) and NH₄⁺–N (S1, 21·4–30·5 mg kg⁻¹; S2, 2·1–23·3 mg kg⁻¹), and NH₄⁺–N (S1, 10·5–28·9 mg kg⁻¹; S2, 5·0–39·0 mg kg⁻¹) in the seedling stage, vegetative growth stage, and reproductive growth stage, respectively. The spatial autocorrelation of AN was strong and was mainly influenced by structural factors during crop growth stages. This was mainly determined by soil erosion–deposition (SED) and soil temperature–moisture (STM) in the seedling stage; this was also mainly influenced by SED, STM, crop type, and crop growth in the vegetative growth stage and by early STM and early SED in the reproductive growth stage. Generally, the content of AN, NO₃⁻–N, and NH₄⁺–N on the whole slope was mainly determined by the early SED and local fertilizer application, while their spatiotemporal heterogeneity, especially the evenness, was mainly changed by SED, STM, crop growth, and crop types on the slope scale. In order to increase more crop yields, additional N fertilizer application on both the summit and the bottom during the vegetative growth stage and conservation tillage systems or additional soil amendments on the back slopes was necessary. Copyright © 2016 John Wiley & Sons, Ltd.     

Release of trace elements from wood ash by nitric acid

Currently wood ash is being used as a soil amendment. Its use is regulated based on trace element content. However, no published information exists on solubilities of trace elements in wood ash. We investigated the release of environmentally-significant trace elements (Cd, Cr, Cu, Pb and Zn) from wood ash as a function of pH and of particle size. Wood ash was sampled from three sources in Maine and sieved into <0.5 mm, 0.5–1 mm, and 1–2 mm fractions. Elemental compositions were determined using a HNO₃/H₂O₂ digestion. Sub-samples (1 g) from each of the nine samples (three sources and three size fractions) were reacted with 50 mLs of standardized HNO₃ for a week using a range of acid concentrations (0.01–0.25 M) to achieve a range in final pH values. The resulting solutions were filtered and analyzed. The compositions of the three wood ashes varied widely. The dominant elements were Si (9.7–34%), Ca (5.8–21%), K (0.8–5.7%), Al (0.8–4.9%), and Mg (0.5–3.0%). Trace elements were present in the following concentrations ranges: Cd (1.9–12 mg kg^?1), Cr (24–92 mg kg^?1), Cu (33–75 mg kg^?1), and Zn (130–1400 mg kg^?1). Both Cd and Zn were released readily from the ashes at final pH values of approximately 6.5 and below. In the final pH range of 3–4, 80–100% of the total Cd and 70–90% of the total Zn was released by the ashes. All three wood ashes showed somewhat different patterns of Cr release. Level of Cr(VI) in a water extract of the ash fractions was found to be a much better predictor of relative Cr solubility than total Cr. Solubility of Cu was low, and Pb was very insoluble. There was little influence of particle size on release of trace elements. The relatively high Cd concentration of wood ash compared with soil, and its relative solubility in wood ash, should be considered in evaluating the potential environmental impact of spreading wood ash on land.     

Application of Organic Wastes in a Soil Polluted with Different Rates of Cr-Pb: Effects on Soil Biological Properties

An experiment was performed to determine the effects of adding municipal solid waste (MSW) and poultry manure (PM) to a soil polluted with chromium (Cr), lead (Pb), and Cr + Pb on the biological parameters of the soil. Soil was mixed with two solutions of Cr(NO₃)₃ and/or Pb(NO₃)₂ to give three concentrations (0, 100, and 250 mg Cr kg^?1 soil and 0, 100, and 250 mg Pb kg^?1 soil) and treated with MSW or PM. When the soil was contaminated with the metals without combining, the greatest adenosine triphosphate (ATP), urease, and phosphatase inhibition percentages occurred for 250 mg Pb kg^?1 soil. When the heavy metals were mixed, the inhibition of the biochemical parameters increased. The application of MSW and PM decreased the inhibition of the biochemical parameters and microbial population in the polluted soils. The inhibition percentage was greater for the soil amended with MSW than with PM, possibly due to the high humic acid concentration.     

Use of the BCR three-step sequential extraction procedure for the study of the partitioning of Cd, Pb and Zn in various soil samples

A slightly modified three-step sequential extraction procedure proposed by the Community Bureau of Reference (BCR) for analysis of sediments was successfully applied to soil samples. Contaminated soil samples from the lead and zinc mining area in the Mezica valley (Slovenia) and natural soils from a non-industrial area were analysed. The total concentrations of Cd, Pb and Zn and their concentrations in fractions after extraction were determined by flame or electrothermal atomic absorption spectrometry (FAAS, ETAAS). Total metal concentrations in natural soils ranged from 0.3 to 2.6 mg kg^-1 for Cd, from 20 to 45 mg kg^-1 for Pb and from 70 to 140 mg kg^-1 for Zn, while these concentrations ranged from 0.5 to 35 mg kg^-1 for Cd, from 200 to 10000 mg kg^-1 for Pb and from 140 to 1500 mg kg^-1 for Zn in soils from contaminated areas. The results of the partitioning study applying the slightly modified BCR three-step extraction procedure indicate that Cd, Pb and Zn in natural soils prevails mostly in sparingly soluble fractions. Cd in natural soils is bound mainly to Fe and Mn oxides and hydroxides, Pb to organic matter, sulphides and silicates, while Zn is predominantly bound to silicates. In contaminated soils, Cd, Pb and Zn are distributed between the easily and sparingly soluble fractions. Due to the high total Cd, Pb and Zn concentrations in contaminated soil close to the smelter, ! and their high proportions in the easily soluble fraction (80% of Cd, 50% of Pb and 70% of Zn), the soil around smelters represents an environmental hazard.     

无机氮与蔬菜废弃物耦合对土壤氮矿化的影响

为探明有机废弃物添加量与不同无机氮水平耦合对土壤氮矿化的影响,设计了3个甘蓝废弃叶添加量[B1:200 g.kg 1(土),B2:400 g.kg 1(土),B3:550 g.kg 1(土)]和4个无机氮水平[N0:0 mg.kg 1(土),N1:25mg.kg 1(土),N2:50 mg.kg 1(土),N3:100 mg.kg 1(土)]交互的控制培养试验(25℃,65%的田间持水量)。试验结果显示:各氮处理下土壤净累积氮矿化量是空白对照的4～5倍,N1水平下土壤净累积氮矿化量显著高于其他氮水平。各甘蓝废弃叶添加量处理下土壤净累积氮矿化量是空白对照的3～5倍,且B2添加量下土壤净累积氮矿化量显著高于B1和B3。统计分析表明,氮处理和甘蓝废弃叶添加量之间的交互效应不显著(P=0.275),甘蓝废弃叶的添加是影响氮矿化的主要因素(Eta2=0.16),而供氮水平为次要因素(Eta2=0.07)。B1添加量下,培养前期(0～20 d)土壤净累积矿化量逐渐升高,后期保持稳定水平;但B2和B3添加量下,培养前期(30 d)土壤呈现矿化、固持、再矿化现象,后期土壤净累积矿化量逐渐升高。氮矿化速率结果说明,甘蓝废弃叶添加后氮素矿化主要发生在培养前30 d。对培养期间土壤净累积氮矿化量随时间变化做一级动力方程模拟,拟合效果良好(R2=0.62～0.89)。     

Effects of Graded Levels of Cadmium on Spinach and Cabbage Grown in an Inceptisol

Cadmium (Cd) contamination of the soil and its concentrations in spinach and cabbage were studied in a pot culture experiment. Eight levels of Cd (0–100 mg kg^?1 soil) were applied singly. Application of Cd of up to 10 and 15 mg kg^?1 resulted in safe Cd concentrations (1.56 and 1.38 mg kg^?1) in the shoots of spinach and cabbage, respectively, at the consumable stage. The total chlorophyll content gradually decreased with the addition of Cd, and the maximum decreases were 31.7 and 32% in spinach and cabbage, respectively, at 60 days of crop growth in the treatment Cd₁₀₀ over the control. The greatest diethylene triamine penta-acetic acid (DTPA)–extractable Cd contents in the postharvest soil of spinach and cabbage were 22.09 and 24.22 mg kg^?1, respectively, in the treatment Cd₁₀₀. The DTPA Cd was significantly negatively correlated with leaf area and total chlorophyll content while positively correlated with root and shoot Cd concentrations of spinach and cabbage.