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We established a field trial to assess the impacts on soil biological properties of application of heavy metal-spiked sewage sludge, with the aim of determining toxicity threshold concentrations of heavy metals in soil. Plots were treated with sludges containing increasing concentrations of Cu, Ni and Zn in order to raise the metal concentrations in the soil by 0-200 mg Cu kg−1, 0-60 mg Ni kg−1 and 0-400 mg Zn kg−1, and were then cultivated and sown in ryegrass-clover pasture and monitored annually for 6 years. All biological properties measured (soil basal respiration, microbial biomass C, and sulphatase enzyme activities), except phosphatase activity, increased in all plots over the duration of the experiment. Consequently, it was only possible to assess effects of heavy metals across time if, each year, all data for each metal were normalised by expressing them as percentages of the activities measured in an un-sludged control plot. When this was done, no significant effects of increasing heavy-metal concentrations on basal respiration, microbial biomass C or respiratory quotient (qCO2) were observed, although total Cu and soil solution Cu were significantly negatively related to microbial biomass C when it was expressed as a proportion of soil total C. None of the properties measured were affected by increasing Ni concentrations. Phosphatase and sulphatase activities were significantly negatively related to increasing Zn concentrations, but not usually to increasing Cu unless they were expressed as a proportion of total C. A sigmoidal dose-response model was used to calculate EC20 and EC50 values using the normalised data, but generally, the model parameters had very large 95% confidence intervals and/or the fits to the model had small R2 values. The factors primarily responsible for confounding these results were site and sample variations not accounted for by the normalisation process and the absence of any data points at metal concentrations beyond the calculated EC50 values. In the few instances where reasonable EC20 values could be calculated, they were relatively consistent across properties, e.g., EC20 for total Zn and phosphatase (330 mg kg−1), total Zn and sulphatase (310 mg kg−1), and EC20 for total Cu and sulphatase (140 mg kg−1) and total Cu and microbial biomass C (140 mg kg−1), when both sulphatase and microbial biomass C were expressed as a proportion of total C. Our results suggest that Cu and Zn at the upper concentrations used in this experiment were possibly having adverse effects on some soil biological properties. However, much higher metal concentrations will be needed to accurately calculate EC20 and EC50 and this may not be easily achievable without many applications of sewage sludge, even if the sludge is spiked with heavy metals. 相似文献
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An immobilized sulphatase reactor column was successfully used to determine the biochemical stability of ester sulphate in soil organic matter extracted from a podzol amended with gypsum. The sulphatase from Helix pomatia was covalently attached to controlled-porosity glass beads, and the immobilized enzyme was packed into a small glass column. The optimum pH, the time required to reach equilibrium, and the percentage of substrate consumed for the enzymatic hydrolysis of soil ester sulphate (pH 7.7, 90 min, 23–59%) were substantially different from those of p-nitrophenyl sulphate at similar concentrations of substrate (pH 7.0, 40 min, 99%). The striking difference in the biochemical stability and kinetic behaviour between soil ester sulphate and the simple synthetic substrate reflected their different chemical nature and structural features. The amounts of enzymatically hydrolysable (labile) ester sulphate in soil organic matter extracted from the podzol amended with gypsum at rates of 0, 50, and 200 kg S ha-1 were significantly different (P=0.0004), being 0.5, 1.1, and 1.4 g S ml-1 soil extract (or 5, 11, and 14 g S g-1 soil), respectively. The labile ester sulphate was not correlated with the total hydriodic acid-reducible organic sulphate with the soil organic matter extracts but with the hydriodic acid-reducible organic sulphate: organic C ratio, which increased as a result of gypsum amendment. This study revealed that input of inorganic sulphate as gypsum substantially increased the accumulation of labile ester sulphate in a podzol. 相似文献
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R. J. Haynes 《Biology and Fertility of Soils》1987,5(3):235-240
Summary The effects of white, black and clear polyethylene mulches on temporal fluctuations in protease, sulphatase and phosphatase activities and levels of available and biomass N, S and P in raised beds of soil under a strawberry crop were investigated under field conditions. During spring, summer and early autumn, clear and, to a lesser extent black, polyethylene mulch increased both maximum and minimum mean monthly temperatures over those recorded with white mulch or no mulch. During summer and autumn, soil moisture content measured at monthly intervals was higher under mulched than unmulched conditions. Levels of extractable nitrate and sulphate in soils during autumn followed the order: clear mulch = black mulch > white mulch > no mulch. However, there were no significant differences in levels of enzyme activity or concentrations of biomass N, S or P between treatments. There were significant seasonal fluctuations in estimates of biomass N, S and P, but there was no close relationship between fluctuations in any estimate. This discrepancy was attributed to errors in the chloroform fumigation technique. Enzyme activities showed significant temporal fluctuations but the three enzymes did not show similar times of minimum and maximum activity. The complexity of interactions between soil microbial and biochemical properties and nutrient availability was exemplified by the absence of a discernible relationship between seasonal fluctuations in enzyme activities and levels of biomass N, S and P and/or levels of extractable mineral N, S and P in the soil. Strawberry fruit yields and vegetative growth followed the order : clear mulch = black mulch>white mulch>no mulch. Clear, and to a lesser extent black mulch increased the percentage of total yields produced in the first 2 months of cropping. 相似文献
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Summary A method of assessing the enzymatic hydrolysis of ester sulphate in soil organic matter was developed. Soil organic matter extracted using a mild, chelating resin extraction procedure was incubated with a sulphatase from Helix pomatia in 0.05 M sodium acetate buffer (pH 4–8) at 37°C for 2h and the sulphate released was determined by a high performance liquid chromatography-conductivity detector system. The effect of some soil factors on the enzymatic hydrolysis of ester sulphate was examined. The study showed that part of the ester sulphate in soil organic matter was biochemically reactive. In the three Podzols studied, the ester sulphate hydrolysed accounted for 2%–12% of the hydriodic acid-reducible organic sulphate extracted. The largest amount of hydrolysable ester sulphate was found in the soil with a low pH, high inorganic sulphate and high hydriodic acid-reducible organic sulphate. 相似文献
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Summary The effects of adding lime and/or phosphate to an acid, phosphate-deficient soil on microbial activity, enzyme activities and levels of biomass and extractable N, S and P were studied under laboratory conditions. Following rewetting there was, as expected, an initial flush in microbial growth and activity, as shown by large increases in CO2 evolution, in levels of biomass N, S and P and by accumulation of extractable mineral N and sulphate in the soil. Following rewetting, additions of lime and phosphate further stimulated mineralization of C, N and S. In the first 4 weeks of incubation, the mineralized N accumulated in the soil as ammonium N and there was a concomitant rise in soil pH. After this initial period, nitrification increased substantially and soil pH decreased again. Additions of lime generally increased protease and sulphatase activities but decreased phosphatase activity. Additions of phosphate decreased the activities of all three enzymes. The positive effect of liming on protease and sulphatase activities persisted for the duration of the experiment while accumulation of mineral N and sulphate effectively ceased after about 4 weeks. Furthermore, although phosphate additions decreased the activities of protease and sulphatase they increased the accumulation of mineral N and sulphate. Thus, protease and sulphatase activities were not reliable indicators of the relative amounts of mineral N and sulphate accumulated in the soil during incubation. Some uncertainty surrounded the validity of biomass S and P values estimated by the chloroform fumigation technique because differing proportions of the sulphate and phosphate released from the lysed cells may have been extracted from the different treatments. 相似文献
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Summary We studied the effect of soil pretreatment, molecular-weight fractionation, and K2SO4 addition on the concentration and biochemical stability of ester sulphate in soil organic matter. A labile ester sulphate fraction (8.1 g S g–1 soil) was detected in the organic matter extracted from a sulphate-rich podzolic sandy loam. This fraction was susceptible to loss during soil pretreatment with water and KCl solution and subsequent extraction of organic matter from the soil. The low-sulphate loam was low in labile ester sulphate (0.6 g S g–1 soil) and the pretreatments had little effect. The addition of K2SO4 to the organic matter extracted from the low-sulphate soil resulted in the formation of appreciable amounts of labile ester sulphate. Newly formed ester sulphate tends to be biochemically less stable than indigenous ester sulphate in soil humic polymers and the ester sulphate associated with the low molecular-weight fractoin of soil organic matter appears to be more susceptible to loss by enzymatic hydroylsis. The results were interpreted in terms of steric effect. Ester sulphate groups bound to external surfaces of soil humic polymers may be easily accessible to sulphatase enzyme and thus readily mineralizable during incubation or extraction of soil organic matter at low soluble-sulphate levels. Sulphate groups on inner surfaces of the organic polymers are shielded from the enzyme due to size exclusion and hence more stable. 相似文献
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