Conservation of mineral nitrogen in restored soils at opencast coal mine sites: II. The effects of inhibition of nitrification and organic amendments on nitrogen losses and soil microbial biomass

Soils stored in stockpiles during opencast mining operations accumulate significant quantities of ammonium (of the order of 200 μg NH₄⁺-N g^?1 soil) within the predominantly anaerobic cores of mounds. Upon stockpile dismantling and land restoration, this NH⁺₄-N is rapidly oxidized to NO^?₃-N, which is readily lost from newly restored soil ecosystems by leaching and denitrification. Experiments were set up to examine how these significant reserves of mineral N might be conserved in such situations. Application of the nitrification inhibitor dicyandiamide was successful in minimizing NO₃^?-N lost by leaching, though large concentrations of NH₄⁺-N were detected in drainage waters. Straw incorporation decreased nitrate leaching by up to 40%; biomass C was some 40% greater in straw-amended than in unamended soils after 14 weeks, though biomass N was similar in both. Addition of nitrogen-free organic materials (glucose, starch and cellulose) produced different results, with glucose amendment showing the greatest reduction in nitrate leaching in the short term (due to an apparent stimulation of denitrification) whereas addition of cellulose resulted in the most effective conservation of nitrogen over 14 weeks; this was due, at least in part, to uptake of mineral N by the soil microbial biomass.     

Effects of nickel addition on nitrogen mineralization,nitrification, and nitrogen leaching in some boreal forest soils

The effects of Ni additions on nitrification, N mineralization, and N leaching were examined in soils from boreal jack pine (Pinus banksiana Lamb.) forests. The results of a series of incubation experiments suggested that under certain conditions, Ni at 100 μg g^?1 soil can stimulate nitrification, and at 500 μg g^?1 can stimulate N mineralization. Nitrification rates were very low overall, but were higher in soils from the vicinity of the Sudbury, Ontario Ni-Cu smelters than in uncontaminated soils. The nitrifier populations, estimated by the most probable number method, were extremely low in uncontaminated soils, but also increased following some Ni additions. Increased leaching of NO_f3 ^p was observed in soil columns treated with Ni. Since N tends to be in low supply in boreal forests, and therefore tightly cycled, the observed disruptions caused by Ni inputs could have an effect on forest productivity.     

Sulfur and nitrogen mineralization in soils compared using two incubation techniques

Net mineralization of sulfur and nitrogen was studied in three Canadian Prairie soils using two commonly used incubation methods. In the open system technique, where the soils were leached periodically II.3–11.8 μ g SO^2?₄ -S g^?1 soil was mineralized in 17 weeks. Little mineralization or a net immobilization of sulfur (from 1.4 to 1.3 μ g SO^2?₄-S g^?1 soil) was observed in a closed system where the soils were left undisturbed throughout incubation. Changes in the specific activity of ³⁵S-labelled soil solution sulfate during the closed incubation indicated that mineralization-immobilization processes were occurring simultaneously resulting in minimal net changes in CaCl₂-extractable SO_2?⁴ concentrations. The amounts of mineralized nitrogen (32.6–57.8 μg N g_?1 soil) were found to be independent of the incubation method employed.     

Soil microbial activity in opencast coal mine restorations

Abstract. A number of restored areas, a soil store and undisturbed areas on opencast coal mine sites, all of similar soil type, were sampled. The microbiological activity (dehydrogenase assay), nitrogen mineralization and nitrifying potentials and physico-chemical characteristics of the soils were determined. Dehydrogenase activities ranged from 140 to 580 μg TPF g^-1 24 h^-1 in undisturbed control soils, whereas the disturbed soils had activities of 10 to 220 μg g^-1 24 h^-1, with the smallest activities being recorded in the stored and most recently reinstated soil, indicating that disturbance has depressed microbial activity. Nitrogen mineralization potential was significantly affected by disturbance, with a value of 18 to 26 μg inorganic N g^-1 21 d^-1 in the soil store and 38 μg^-1 21 d^-1 in a soil reinstated for six months, although the values were less than this in soils reinstated for up to six years. Nitrifying potential was not significantly less in the stored soils, being within the range of 60 to 135 μg nitrate N formed g^-1 soil 21 d^-1, which was similar to that found in the undisturbed control soil. The water-holding capacity was less in the stored soil than the undisturbed controls, and was significantly less in soil reinstated for 1.5 to 2.5 years, being only 65% of the undisturbed value (0.66 g water g^-1 soil). Ammonium content of the soil store was one hundred fold larger in the soil store than in the controls (0.6 to 1.7 μg ammonium N g^-1). The carbon contents in the control soils ranged from 4.5 to 7.2%, whereas the stored and reinstated soils had generally less amounts ranging from 1.6 to 5.8%. There was a significant and positive correlation between water-holding capacity and nitrifying potential. The implications for long-term restoration are discussed.     

Effects of nitrogen dioxide on selected soil processes

Nitrogen dioxide gas was rapidly absorbed by soil. After a 15 min incubation at 25°C, soil at a moisture content of 16% absorbed 99% of the NO₂ introduced into the gas-phase volume of a closed system. The presence of microorganisms hatl no influence on the rate of absorption of the gas by soil. The absorption of NO₂ by sandy clay loam soil was not an oxygen- or temperature-dependent process nor did it depend upon the moisture content of the soil. These physical factors acquired significance only in determining the initial rate of absorption of the gas and the rate at which NO₂ diffused through the soil. Exposure of soil to NO₂ resulted in substantial increases in the levels of NO _inf2 ^sup? N in the soil. Chemical oxidation of the NO _inf2 ^sup? N resulted in an increase in NO _inf3 ^sup? N levels. During a 14-day incubation, NO _inf2 ^sup? N concentrations in sterile soil exposed to an atmosphere containing 100 μg ml^?1 of NO₂ decreased from 190 μg g^?1 of soil to 105 μg g^?1 with an accompanying increase in NO _inf3 ^sup? N from 2 μg g^? ₁ to 63 μg g^?1 of soil. Nitrogen dioxide severely inhibited the growth of both aerobic and anaerobic asymbiotic N₂-fixing bacteria in soil. After a 48 h incubation at 25°C, soil aggregates exposed to an atmosphere containing 100 μg ml^?1 of NO₂ contained 88% and 98% fewer aerobic and anaerobic N₂-fixing bacteria, respectively. C₂H₂-reduction measurements showed that nitrogenase synthesis and activity in artificial soil aggregates amended with 2% glucose were inhibited by 20% and 48%, respectively, when exposed to atmospheric concentrations of 35 and 3.5 μg ml^?1 of NO₂, respectively.     

Mineralization and immobilization of nitrogen in fumigated soil and the measurement of microbial biomass nitrogen

Immobilization of N was measured in a fumigated and in an unfumigated soil by adding (¹⁵NH₄)₂SO₄ and following the disappearance of inorganic label from the soil solution and its simultaneous conversion to soil organic N. Calculations based on the measurement of organically-bound ¹⁵N gave more consistent values for immobilization than did calculations based on the measurement of the disappearance of label from solution. The fumigated soil immobilized 6.6 μg N g^?1 N g^?1 soil in 10 days at 25°C, the unfumigated control 4.8 μg. The corresponding gross mineralization rates were 34.9 and 5.6 μg N g^?1 soil in 10 days.Addition of 58 μg N as (¹⁵NH₄)₂SO₄ to the fumigated soil increased the quantity of the ynlabelled NH₄-N extracted at the end of 10 days from 33.8 to 37.8 μg Ng^?1 soil, i.e. there was a positive Added Nitrogen Interaction (ANI). The added labelled N produced this ANI, not by increasing the rate of mineralization of organic N, but by standing proxy for unlabelled N that otherwise would have been immobilized.A procedure for calculating biomass N from the size of the flush of mineral N caused by fumigation is proposed. Biomass N (B_N) is calculated from the relationship B_N = F'_N/0.68 where F'_N is [(N in fumigated soil incubated for 10 days — (N in unfumigated soil incubated for 10 days)].     

Effect of the herbicide fluazifop-butyl on fungal populations and activity in soil

The side effects of fluazifop-butyl on soil fungal populations and oxygen uptake were studied by incubating soil samples with a range of fluazifop-butyl concentrations (0, 0.6, 3 and 6 μg g^?1) over 8 weeks. Cellulose decomposition in soil was also studied in laboratory experiments with the herbicide which was either incorporated in soil or sprayed onto calico squares which were buried in soil. The mycelial dry weight of six fungal species under the effect of the herbicide was also examined. Fluazifop-butyl had no significant effect on total fungal propagule populations at 0.6 μg g^?1. At 3 and 6 μg g^?1, it caused temporary reduction in fungal populations observed after 1 and 2-wk of incubation. The herbicide had no significant effect on OZ uptake. The decay of calico buried in herbicide-treated soil was generally stimulated, while the decomposition of herbicide-treated calico, buried in untreated soil, was temporary delayed. The mycelial dry weight yields of Aspergillus favus (at 2 and 12 μg mL^?1 of fluazifop-butyl) and Cunninghamella echinulata (at 12 μg mL^?1) were significantly increased. At 24 μg mL^?1 the mycelial dry weight of A. flavus and Alternaria alternata was significantly reduced.     

Forms of trace metals from inorganic sources in soils and amounts found in spring barley

Barley (Hordeum vulgare L.) was grown on a sandy soil given different doses of cadmium carbonate (salt), copper carbonate (malachite), lead carbonate (cerussite), and zinc carbonate (smithsonite) in a pot experiment conducted in a greenhouse. The element compounds were added to the soil in amounts equivalent to the following levels of the metals: Cd 5, 10, 50 μq ^?1; Cu and Pb 50, 100, 500 μg g^?1; Zn 150, 300, 1500 μg g^?1. Sequential extraction was used for partition these metals into five operationally-defined fractions: exchangeable, bound to carbonates, bound to Fe-Mn oxides, bound to organic matter and residual. The residue was the most abundant fraction in the untreated soil for all the metals studied (43 to 61% of the total contents). The concentration of exchangeable Cd (0.2 μg g^?1), Cu (0.01 μg g^?1), Pb (0.1 μg g^?1), and Zn (1.4 μg g^?1) were relatively low in the untreated soil but increased markedly in the treated soils for Cd (up to 31 μg g^?1) and Zn (up to 83 μg g^?1), whereas only small changes were observed for Cu and Pb. The pot experiment showed a significant increase in the Cd and Zn contents of barley grown on the treated soils, but only small changes in Cu and Pb concentrations.     

Effects of pentachlorophenol on asymbiotic nitrogen fixation in soil

The effect of 50, 100, 150, and 400 μg sodium pentachlorophenate (Na-PCP) per gram soil was studied in nonsterile soil incubated under aerobic and anaerobic conditions, and in sterilized soil inoculated withAzotobacter sp. isolated from the soil. N₂ fixation was determined by acetylene reduction. Pentachlorophenate at a concentration of 50 μg g^?1 had an inhibitory effect in nonsterile soil incubated aerobically while strong inhibition of dinitrogen fixation in nonsterile soil occurred in the presence of 100 μg g^?1 and above. The EC₅₀ values for the inhibition of nitrogenase activity in nonsterile soil incubated aerobically and anaerobically and in sterilized soil inoculated withAzotobacter sp. suspensions were 49.8±1.4 μg Na-PCP g^?1, 186.8±2.8 μg Na-PCP g^?1, and 660.8±29.3 μg Na-PCP g^?1, respectively.     

Effects of the herbicide glyphosate on nitrogen cycling in an acid forest soil

The herbicide glyphosate was sprayed aerially on a section of conifer forest in Atlantic Canada that had been previously clearcut and reforested. Glyphosate was then tested for effects on ammonification, nitrification, and denitrification for a period of 8 months by comparing microbial activity in treated and untreated zones of the clay loam forest soil and the overlying decomposing litter, both with a pH of 3.8. With ammonification, there was generally a stimulation of activity in both the forest litter (FL) and forest soil (FS) that had been exposed to glyphosate during spraying. Nitrification rates in FL and FS were very low and glyphosate had no appreciable stimulatory or inhibitory effect on nitrification. Although glyphosate stimulated denitrification in a few instances, it generally had no significant effect on denitrification activity in FL and FS exposed during spraying. With all processes, microbial activity in FL was significantly greater than that in FS. Laboratory bioassays were also performed with FL and FS, as well as two silt loam (pH 5.8 and 6.4) and one sandy loam (pH 6.8) agricultural soils, using glyphosate concentrations up to 200 times higher than field application rates. With ammonification and denitrification, glyphosate generally stimulated activity at all levels tested and in all soil used. Glyphosate stimulated ammonification by 50% at concentrations ranging from 140 to 550 μg g^?1 for the soils and >4000 μg g^?1 for FL. With denitrification, the corresponding herbicide levels were approximately 2250 μg g^?1 for FS, > 10,000 for FL, and 450 for an agricultural soil. With nitrification, it was estimated that glyphosate concentrations greater than 1000 to 2000 μg g^?1 would be required to cause a 50% inhibition of activity. The careful use of glyphosate in forestry should have no toxic effects on N cycling in soils.     

Immobilization and mineralization of nitrogen in soils incubated with pig slurry or ammonium sulphate

Nitrogen mineralization and immobilization were investigated in two soils incubated with ammonium sulphate or pig slurry over a range of temperatures and moisture contents. A reduction in the mineralization of soil organic N was observed in soils incubated with 100 μg NH₄⁺-Ng^?1 soil as ammonium sulphate at 30°C but not at lower temperatures. Addition of 100 μg NH₄⁺-N g^?1 soil as pig slurry resulted in a period of nett immobilization lasting up to 30 days at 5°C. Although the length of the immobilization phase was shorter at higher temperatures the total N immobilized was similar. The subsequent rate of mineralization in slurry-treated soils was not significantly greater (P = 0.05) than in untreated soils. There was no evidence of any subsequent increased mineralization arising from the immobilized N or slurry organic N for up to 175 days. The rate of immobilization was found to increase with increasing moisture content, though the period of nett immobilization was shorter, so that the amount of N immobilized was similar over a range of moisture contents from 10 to 40%. Approximately 40% of the NH₄⁺-N in the slurry was immobilized under the incubation conditions used.     

Estimation of the adenylate energy charge in unamended and amended agricultural soils

To determine relatively low concentrations of adenine nucleotides in agricultural soils a NaHCO₃-based extradant was developed and compared with the trichloroacetic acid-paraquat-phosphate extradant. The new medium, consisting of chloroform, sodium bicarbonate, phosphate and adenosine (pH 8.0) gave soil extracts which could be investigated without further neutralization and dilution. ATP was measured directly in the soil extracts by the luciferin-luciferase system. ADP and AMP were estimated after their enzymatic conversion to ATP by standard methods. The quantities of nucleotides corrected for recovery of standards were used to calculate the adenylate energy charge (AEC) from the formula AEC = [ATP] + 1/2[ADP]/[ATP] + [ADP] + [AMP], The AEC was estimated in six unplanted soils from agricultural fields. A very similar energy charge of 0.3-0.4 was found in all soils sampled which indicates a low metabolic activity of the soil population. Two other soils with a pronounced difference in biomass-C content were used to investigate the influence of different amendments on the AEC. In an experiment with low glucose supplements up to 500 μg C g^?1 soil, the soil with the low biomass-C (a cambisol) showed a distinct increase of the AEC from 0.34 to 0.50, whereas the soil with the high biomass-C content (a phaeozem) increased its AEC only slightly from 0.32 to 0.37. In another experiment with high glucose supplements the phaeozem reached its maximum AEC value of 0.56 after the addition of 4000 μg Cg^?1 soil. An amendment with 8000 μg C g^?1 soil gave no further increase. In the combisol the addition of 1000 μg C g^?1 soil increased the AEC to 0.61. Higher supplements gave only a slight further increase to a maximum value of 0.67 after the addition of 8000 μg C g^?1 soil. The same AEC value was reached when the cambisol was amended with a mixture of organic substrates at a concentration of 10,000 μg C g^?1 soil.     

Patterns of trace metal concentration and acidity in montane forest soils of the northeastern United States

Forest floor and mineral soil samples were collected from subalpine spruce-fir forests at 1000 m above mean sea level on 19 mountains in the northeastern United States to assess patterns in trace metal concentrations, acidity, and organic matter content. The regional average concentrations of Pb, Cu, and Zn in the forest floor were 72.3 (2.9 s.e.) μg g^?1, 8.5 (0.7) μg g^?1, and 46.9 (2.0) μg g^?1, respectively. The regional average concentrations of Pb, Cu, and Zn in the mineral soil were 13.4 (0.8) μg g^?1, and 18.2 (1.2) μg g^?1, respectively. The regional average pH values of the forest floor and mineral soil were 3.99 (0.03), and 4.35 (0.03), respectively. The Green Mountains had the highest concentrations of Pb (105.7 μg g^?1), and Cu (22.7 μg g^?1), in the forest floor. They also had the highest concentrations of Cu (18.0 μg g^?1), in the mineral soil. Site aspect did not significantly influence any of the values. Concentrations of Pb were lower than concentrations reported earlier in this decade at similar sites while concentrations of Cu and Zn remained the same. We believe that these lower Pb concentrations reflect real changes in forest Pb levels that have occurred in recent years.     

A field study of gross rates of N mineralization and nitrification and their relationships to microbial biomass and enzyme activities in soils treated with dairy effluent and ammonium fertilizer

Abstract. Gross N mineralization and nitrification rates were measured in soils treated with dairy shed effluent (DSE) (i.e. effluent from the dairy milking shed, comprising dung, urine and water) or ammonium fertilizer (NH₄Cl) under field conditions, by injecting ¹⁵N-solution into intact soil cores. The relationships between gross mineralization rate, microbial biomass C and N and extracellular enzyme activities (protease, deaminase and urease) as affected by the application of DSE and NH₄Cl were also determined. During the first 16 days, gross mineralization rate in the DSE treated soil (4.3–6.1 μg N g^?1 soil day^?1) were significantly (P 14;< 14;0.05) higher than those in the NH₄Cl treated soil (2.6–3.4 μg N g^?1 soil day^?1). The higher mineralization rate was probably due to the presence of readily mineralizable organic substrates in the DSE, accompanied by stimulated microbial and extracellular enzyme activities. The stable organic N compounds in the DSE were slow to mineralize and contributed little to the mineral N pool during the period of the experiment. Nitrification rates during the first 16 days were higher in the NH₄Cl treated soil (1.7–1.2 μg N g^?1 soil day^?1) compared to the DSE treated soil (0.97–1.5 μg N g^?1 soil day^?1). Soil microbial biomass C and N and extracellular enzyme activities (protease, deaminase and urease) increased after the application of the DSE due to the organic substrates and nutrients applied, but declined with time, probably because of the exhaustion of the readily available substrates. The NH₄Cl application did not result in any significant increases in microbial biomass C, protease or urease activities due to the lack of carbonaceous materials in the ammonium fertilizer. However, it did increase microbial biomass N and deaminase activity. Significant positive correlations were found between gross N mineralization rate and soil microbial biomass, protease, deaminase and urease activities. Nitrification rate was significantly correlated to biomass N but not to the microbial biomass C or the enzyme activities. Stepwise regression analysis showed that the variations of gross N mineralization rate was best described by the microbial biomass C and N.     

Crop-specific differences in the concentrations of lipids in leachates from the root zone

Although lipids are involved in diverse soil processes and affect various soil properties, the contribution of rhizodeposits and the root zone to lipid concentrations and distributions in soils is unknown. For the first time, we determined the concentrations of alkanoic acids, n-alkanes and n-alkenes in root zone leachates and roots of maize and potato using gas chromatography/mass spectrometry (GC/MS). In total, the lipid concentrations of leachates were 100 μg g^?1 (maize) and 17 μg g^?1 (potato). The saturated n-alkanoic acids, ranging from n-C₁₄ to n-C₂₈ and having the maximum at n-C₂₂ (maize) and at n-C₁₆ (potato), were more abundant than the other compounds. Maize leachates had more alkanes (20 μg g^?1) than potato leachates (3.1 μg g^?1), but the members of the homologues were nearly the same. Comparison of these distributions with data for roots, microorganisms and soil indicated that the lipids in the leachates from the root zone mainly originated from abrasion of fine roots, rhizodeposits and rhizosphere microorganisms.     

Liming effects on some chemical and biological parameters of soil (spodosols and histosols) in a hardwood forest watershed

Acidic lakes and streams can be restored with base application (usually limestone) provided that the base does not wash out before the benefits of alkalization can be realized; liming soils of the adjoining watershed may be an alternative approach. This study was conducted to provide a scientific basis for soil liming. Plots (50 m²) with different limestone dosages (e.g. 0, 5, 10 or 15 Mg CaCO₃ ha^?1) were established on each of two different soils (a Spodosol and a Histosol) in the Woods Lake watershed of the Adirondack Park Region of New York, USA. Six months after soil liming much of the added limestone was still present in both the Spodosol and in the Histosol. Ten months after soil liming results indicated that: (1) soil pH increased (>1 unit) but mostly in the top 1 cm; (2) net N mineralization increased from 9.6 to ca. 15 µg N g^?1 d^?1 and nitrification increased from 2.8 to ca. 8 µg N g^?1 d^?1; (3) denitrification was not affected (98 µg N g^?1 d^?1); (4) CO₂ production potential decreased in the surface soil and as a function of limestone dosage (60 to 6 µmol g^?1 d^?1); and (5) soluble SO ₄ ^2? concentrations in the Histosol were not affected (105 µmol L^?1). Liming acidic forest soils with >5 Mg CaCO₃ ha^?1 may increase the soil's acid neutralizing capacity, which could provide long-term benefits for surface water acidification.     

Fungal flora of soil polluted with copper

The effects of copper pollution on the soil fungal flora was investigated. Soils treated with 100, 200, 400, 800 or 1600 μg Cu g^?1 were used for experiments to study changes in fungal populations, especially the development and dominance of copper-tolerant fungi. Fungi were sampled 1, 3 and 5 months after copper treatment.All the correlation coefficients between the copper contents and the number of fungal colonies plated were positive. The higher the copper concentration in soil, the more 1000 μ Cu ml^?1 tolerant fungi were isolated. The relative number of 1000 μg Cu mr^?1 tolerant fungi from the soil treated with 1600 μg Cu g^?1 was about 30% of those of the control 14 days after treatment. Within the limits of this experiment, the increase in fungal populations was directly correlated with the increase of dominant Cu-tolerant fungi.From control soils, containing low quantities of copper, 1000 μg Cu ml^?1 tolerant fungi were also isolated; whereas, from soils containing high amounts of copper, some Cu-sensitive fungi were isolated. Most of the 1000 μg Cu ml^?1 tolerant fungi were Penicillium spp. It was concluded that the genus Penicillium may be dominant in soils polluted with copper.     

Nitrous oxide emission as affected by alternate anaerobic and aerobic conditions from soil suspensions enriched with ammonium sulfate

The effect of several anaerobic and aerobic cycles of varying duration on N₂O emission and labelled N loss was investigated in (¹⁵NH₄)₂SO₄ amended soil suspensions. No N₂O was evolved from the continuously-anaerobic treatment. The continuously-aerobic treatment produced approximately 0.8 μg N₂O-N g^?1 dry soil in 56 days. Alternate anaerobic-aerobic cycles increased the net N₂O evolution with 7.2 μg N₂O-N g^?1 dry soil produced in 56 days from the 7-day anaerobic, 7-day aerobic treatment. The net N₂O evolution increased further when the duration of the anaerobic and aerobic periods was increased from 7-7 days to 14-14 days (15.7μg N₂O-N g^?1 dry soil in 56 days), although the total ¹⁵N loss from the system was approximately the same for the two treatments. The results of this study show that N₂O evolution from soils is likely to be greater under fluctuating moisture conditions than under either continuously well-aerated conditions, or continuously excess-moisture conditions.     

Effect of elevated concentrations of Cd and Zn in soil on spring wheat yield and the metal contents of the plants

The effect of increasing concentrations of Cd and Zn in a sandy soil on spring wheat (Triticum vulgare L.) yields and the metal contents of the plants was examined in a pot experiment to establish critical levels of these metals in soil. The metals were added (individually and jointly) to the soil as sulfates in the following doses (in μg g^?1, dry wt.): Cd — 2, 3, 5,10, 15, 25, and 50; Zn ?200, 300, 500, 1000, 1500, 2500, and 5000. Cadmium added to soil did not affect yields of wheat. The Zn dose of 1000 μg g^?1 strongly reduced crop yields; at 1500 μg g^? Zn dose wheat did not produce grain. The metal contents of wheat increased with increasing concentrations of Cd and Zn in soil up to 10.3 and 1587 μ g^? of Cd and Zn in straw, respectively. The concentrations of both metals were higher in straw than in grain by factors of 3–7 and 1.5–2 for Zn and Cd, respectively. The relationships between Cd and Zn contents of the plants and soils were best expressed by exponential equations. High concentrations of Zn in soils (1042 and 1542 μg g^?1) enhanced uptake of Cd by plants. The tested threshold concentrations of the metals in soils (3 μg g^?1 for Cd and 200–300 μg g^?1 for Zn) are safe for Zn but are too high for Cd in terms of protecting plants from excessive metal uptake. The critical Cd content of sandy soil should not exceed 1.5 μg g^?.     

Soil lead concentrations in residential Minnesota as measured by ICP-AES

A total of 2454 samples were collected to evaluate the degree, extent, and distribution of Pb contaminated soil in Minnesota. Samples were collected primarily at locations where susceptible populations were concentrated. Soil Pb concentrations in chilldren's play areas, urban gardens, and at open sites were generally below 100 μg g ^?1 when Pb painted structures were absent. Street side and yard soils typically had Pb concentrations between 10 to 300 μg g^?1, with samples collected near major highways or Pb painted structures exhibiting greater values. The most severely contaminated soils were found in localized areas around the foundations of private residences, where concentrations up to 20 136 μg g^?1 were detected. Exterior Pb based house paint is the major Pb source in these soils, and its presence greatly influences the distribution of contaminated soil in individual yards. Contamination attributable to autoemissions is less concentrated but more widespread than contamination from paint. A higher proportion of soils exceeding 1000 wg g^?1 Pb was found in large cities than elsewhere. However, a sufficient number were detected in small cities and rural areas to confirm that high soil Pb levels are not exclusively an urban phenomenon. By examining the degree, extent, and distribution of Pb contaminated soils in Minnesota, this study provides information useful in guiding response actions to reduce children's exposure to Pb by this pathway.