Pb-Zn交互作用对红壤微生物生物量的影响

A laboratory incubation experiment was conducted to evaluate the effects of lead and zinc applied alone or in various combinations on the size of microbial biomass in a red soil. Treatments included the application of lead at six different levels i. e., 0 (background), 100, 200, 300, 450 and 600 g g^-1 soil along with each of the four levels of zinc (0, 50, 150 or 250 g g^-1 soil). Application of lead or zinc alone to soil significantly (P < 0. 001) affected the soil microbial biomass. The microbial biomass carbon (C_mic), biomass nitrogen (N_mic) and biomass phosphorus (P_mic) decreased sharply in soils contaminated with lead or zinc. Combined application of lead and zinc resulted in a greater biocidal effect on soil microbial biomass, which was significantly higher (P < 0. 001) than that when either lead or zinc was applied alone. Consistent increase in the biomass C: N and decline in the biomass C:P ratios were also observed with the increased metal (Pb and Zn) toxicity in the soil.     

γ-辐照对施用碱稳定固体土壤中Cu的提取性影响

An incubation experiment was conducted to investigate the microbial biomass associated Cu in four contrasting soils to which an alkaline stabilised sewage sludge cake was applied. The organisms of sludge-amended and control soils were killed using γ-irradiation technique, and the aqueous and acid-extractable Cu concentrations were determined. Addition of the sludge product increased significantly the concentration of both the aqueous and dilute HOAc-extractable Cu in all the irradiated soils compared to the non-sterilised sludge/soil mixtures, but the increase was more pronounced in the dilute acid-extractable Cu, indicating thatthe Cu rendered extractable in water and dilute acetic acid by γ-irradiation existed in the both soil liquidand solid phases. The additional increase in extractable Cu following the biocidal treatment is likely to bedue to release of Cu from the same fraction of soil microbial biomass.     

磷的吸附和表面电荷特征及其与华南地区某些土壤矿物的关系

The phosphate adsorption and surface charge characteristics of the tropical and subtropical soils derived from different parent materials in China were determined, and their relations to soil mineralogy were analysed. The results showed that all soil phosphate adsorption curves were well fitted by Freundlich equation and Langmuir equation. The maximum buffering capacity of P ranged from 66 to 9 880 mg kg^-1, with an increasing order of purple soil, skeletal soil, red soil, lateritic red soil, yellow soil and latosol; and the highest value was 149 times the lowest value, which indicated great differences among these soils in phosphate adsorption and supplying characteristics. The pH₀ (zero point of charge) values obtained by salt titration-potential titration varied from 3.03 to 5.49, and the highest value was found in the latosol derived from basalt whereas the lowest value was found in the purple soil. The correlation analysis indicated that the main minerals responsible for phosphate adsorption in the soils were gibbsite, amorphous iron oxide and kaolinite; and the pH₀ was mainly controlled by kaolinite, gibbsite and oxides.     

长期稻秆还田对土壤微生物量及C、N动力学的影响

A study was performed on the long-term effect of straw incorporation on soil microbial biomass C contents, C and N dynamics in both Rothamsted and Woburn soils. The results showed that for both soils, the microbial biomass C contents were significantly different among all the treatments, and followed the sequence in treatments of straw chopped and incorporated into 10 cm (CI10) > straw burnt and incorporated into 10 cm (BI10) > straw chopped and incorporated into 20 cm (CI20) > straw burnt and incorporated into 20 cm (BI20). Laboratory incubation of soils showed that the cumulative CO₂ evolution was closely related to the soil microbial biomass C content. Carbon dioxide evolution rates (CO₂-C, μg (g•d)^-1) decreased rapidly in the first two weeks' incubation, then decreased more slowly. The initial K₂SO₄-extractable NH₄-N and NO₃-N contents were low and similar in all the treatments, and all increased gradually with the incubation time. However, net N immobilization was observed in chopped treatments for Rothamsted soils during the first 4 weeks. Nevertheless, more N mineralization occurred in Treatment CI10 than any other treatment at the end of incubation for both soils. The Woburn soils could more easily suffer from the leaching of nitrate because the soils were more permeable and more N was mineralized during the incubation compared to the Rothamsted soils.     

施入粉煤灰和污泥对酸性淋溶土镉和铅吸附的影响

The safe recycling of fly ash (FA) and sewage sludge (SS) in the agricultural processes comprises an important environmental technology on waste management. Soils amended with FA and SS may change their ability to adsorb heavy metals due to either increase of soil pH or decomposition of sludge-borne organic matter. Thus, Cd and Pb sorption was investigated by 1-month incubation under soil moisture content at field capacity and room temperature with an acidic Typic Haploxeroalf from central Greece amended with varying amounts of FA and SS. Batch experiments were conducted by equilibrating the soil samples with CaCl₂ solutions containing 0-400 mg Pb L^-1 or 0-100 mg Cd L^-1. The results showed that the Freundlich equation described well the Cd and Pb sorption. Distribution coefficient (K_d) values of Pb were higher than those of Cd in all the treatments of this study. Application of FA increased K_d values for Cd and Pb to 8.2 and 2.3 times more than the controls, respectively. Simultaneous applications of FA and SS caused a K_d increase of 3.8 and 2.1 times compared to the treatments that received only SS for Cd and Pb, respectively. Treatment of SS alone did not significantly change Cd and Pb sorption compared to the controls. The sorption reactions seemed to be mainly affected by soil pH, which was revealed by the significant correlations of Cd and Pb sorption with soil pH. These suggested that fly ash was very useful as a low-cost adsorbent for Cd and Pb and could be used as an ameliorant for biosolid-amended acidic soils.     

中国土壤微生物量的大小

The microbial biomass C, N and P of soils all over China were determined in this study to study their affecting factors. The results, about 100-417 mg C kg^-1 soil, 18-51 mg N kg^-1 soil and 4.4-27.3 mg P kg^-1 soil, showed the biomass C, N and P in linear relationship with the soil total organic C, toal N and soil organic P. The ratios of C: N and C:P, ranging from 5.6 to 9.6 and from 11.2 to 48.4 respectively, were affected by soil pH, texture, crop rotation, macroclimate, etc. The ratio of C:N in soil biomass increases gradually from the north to the south in China.     

黄土高原某些耕作土壤中土壤微生物生物量C、N与矿化N的关系

The chloroform fumigation-incubation method was used to measure the soil microbial biomass C (SMBC) and N (SMBN) in 16 loessial soils sampled from Ansai, Yongshou and Yangling in Shaanxi Province. The SMBC contents in the soils ranged from 75.9 to 301.0 μg C g^-1 with an average of 206.1 μg C g^-1, accounting for 1.36%~6.24% of the total soil organic C with an average of 3.07%, and the SMBN contents from 0.51 to 68.40 μg N g^-1 with an average of 29.4 μg N g^-1, accounting for 0.20%~5.65% of the total N in the soils with an average of 3.36%. A close relationship was found between SMBC and SMBN, and they both were positively correlated with total organic C, total N, NaOH hydrolizable N and mineralizable N. These results confirmed that soil microbial biomass had a comparative role in nutrient cycles of soils.     

较贫瘠的红壤中有机质的积累及其生态意义

Field experiments on the decomposition of organic materials and the accumulation of organic carbon in infertile red soils were conducted at the Ecological Experimental Station of Red Soil, the Chinese Academy of Sciences, and the potential of CO₂ sequestration by reclamation and improving the fertility of these soils was estimated. Results showed that in infertile red soils, the humification coefficients of organic materials were rather high, ranging from 0.28 to 0.63 with an average of 0.43, which was 41% higher than those in corresponding red soils with medium fertility. This was mainly attributed to the high clay content, high acidity and low native organic matter content of infertile red soils. Compared to those in corresponding normal red soils, the decomposition rates of organic materials were significantly lower in infertile red soils in the first 2 years, thereafter no significant difference was observed between those in the two kinds of soils. Depending on the kind and amount of organic manure applied, the soil properties and the rotation systems, annual application of organic manure with a rate of 4 500 to 9 000 kg ha^-1 increased the organic carbon content in surface 20 cm of infertile red soils by 2.1~7.5 g kg^-1 with an average of 4.7 g kg^-1 within the first 5 years. The organic carbon content in infertile red soils which received organic manure annually increased linearly in the first 10 years, thereafter it slowed down, implying that the fertility of the infertile red soils could reach middle or high level in 10 years if the soil was managed properly. It was estimated that through exploitation of wastelands, re-establishment of fuel forests and improvement of soil fertility, soils in red soil region of China could sequester an extra 1.50 × 10¹⁵ g of atmospheric CO₂.     

玉米秸秆应用和腐化对钙质苏打土改良的影响: 实验室试验研究

A laboratory lysimeter experiment was conducted to investigate the effects of forage corn (Zea mays L.) stalk application on the CO₂ concentration in soil air and calcareous sodic soil reclamation. The experimental treatments tested were soil exchangeable sodium percentage (ESP) levels of 1, 11, and 19, added corn stalk contents of 0 to 36 g kg^-1, and incubation durations of 30 and 60 days. The experimental results indicated that corn stalk application and incubation significantly increased CO₂ partial pressure in soil profile and lowered pH value in soil solution, subsequently increased native CaCO₃ mineral dissolution and electrolyte concentration of soil solution, and finally significantly contributed to reduction on soil sodicity level. The reclamation effciency of calcareous sodic soils increased with the added corn stalk. When corn stalks were added at the rates of 22 and 34 g kg^-1 into the soil with initial ESP of 19, its ESP value was decreased by 56% and 78%, respectively, after incubation of 60 days and the leaching of 6.5 pore volumes (about 48 L of percolation water) with distilled water. Therefore, crop stalk application and incubation could be used as a choice to reclaim moderate calcareous sodic soils or as a supplement of phytoremediation to improve reclamation effciency.     

土壤中有效结合态氨的一种测定方法

Dynamics of fixed NH₄⁺ in NH₄⁺-treated soils incubated with glucose at 37±2 ℃ during the course of incubation and factors affecting it were studied. Results showed that content of fixed NH₄⁺ in soil reached a minimum on day 7 after incubation and then increased gradually regardless of the amount of glucose added and the kind of soil tested. However, the amount of fixed NH₄⁺ released from the soil at the given time varied with both the amount of glucose added and the kind of soil examined. In cases glucose was added at a rate of 10.0g C/kg soil, the amount of fixed NH₄⁺ retained in soil after 7 days of incubation was almost identical to that found by Neubauer test. Addition of K⁺ depressed the release of fixed NH₄⁺ significantly. Based on the results obtained a method for determining the content of available fixed NH₄⁺ in soils was proposed and the amount of N as available fixed NH₄⁺ in two soils measured by this method on an area profile-depth basis was presented.     

红壤微生物生物量C周转及其研究

采用14 C底物标记技术测定了三种不同质地 (红砂土菜地、黄筋泥桔园和茶籽园 )的红壤微生物生物量C的周转期。结果表明 ,在 2 5℃、5 0 %田间持水量培养条件下 ,三种红壤微生物生物量C的周转期分别为 80天、1 39天和 1 70天。周转期与粘粒含量关系较为密切 ,砂质土壤的周转期较粘粒土壤短 ,提示砂质土壤有机质易被微生物降解 ,有利于养分的迅速释放 ,而粘粒土壤则更有利于养分的持留。周转期与利用方式、pH以及有机质含量无明显相关。红壤微生物生物量C周转期总体上较报道的其他类型土壤微生物生物量C周转期短 ,表明热带—亚热带地区酸性红壤有机质和养分周转相对较快 ,这有可能是造成红壤养分贫瘠的一个原因。根据周转期估算 ,通过微生物年周转的C量 (即年流通量 )为微生物生物量C的 2倍以上     

Determination of soil microbial biomass phosphorus in acid red soils from southern China

A CHCl₃ fumigation and 0.03 M NH₄F-0.025 M HCl extraction procedure was used to measure microbial biomass P (P_mic) in 11 acid red soils (pH <6.0) from southern China and the results compared to those obtained by the commonly-used CHCl₃ fumigation and 0.5 M NaHCO₃ extraction method. Extraction with NH₄F-HCl was found to be more effective and accurate than NaHCO₃ extraction for detecting the increase of P from microbial biomass P following chloroform fumigation due to its higher efficiency in extracting both native labile phosphate and added phosphate (³²P) in the soils. This was confirmed by the recovery of ³²P from in situ ³²P-labeled soil microbial biomass following fumigation and extraction by the NH₄F-HCl solution. Soil microbial biomass P, measured by the NH₄F-HCl extraction method, was more comparable with soil microbial biomass C (with a more narrow C:P ratio range of 4.3 to 22.3 and a mean of 15.6 in the microbial biomass), than that obtained by NaHCO₃ solution (with a mean C:P ratio of 30.7 and a wide range of 14.9 to 48.9). K_p, the fraction of soil microbial biomass P extracted after CHCl₃ fumigation, by the NH₄F-HCl solution was 0.34. The amount of microbial biomass P determined (using K_p =0.34) was 3–400% (mean 131%) higher than that obtained by the NaHCO₃ extraction (using K_p =0.40) for the 11 red soils studied. The results suggest that the CHCl₃ fumigation and NH₄F-HCl extraction method is more reliable for measuring microbial biomass P than the NaHCO₃ extraction method in acid red soils.     

Microbial use of lignite compared to recent plant litter as substrates in reclaimed coal mine soils

In the Lusatian mining district, rehabilitated mine soils contain substantial amounts of lignite in addition to recent carbon derived from plant litter. The aim of this study was to examine the importance of the two organic matter types as substrates for soil microbial biomass in mine soils containing organic matter with a contrasting degree of humification. Samples were taken from the lignite-containing overburden material, from a mine soil under 14-year-old black pine (Pinus nigra) and from a mine soil under 37-year-old red oak (Quercus rubra). Overburden material was ameliorated with alkaline ash and incubated in an identical manner as the 14-year-old and 37-year-old mine soils for 16 months. Carbon mineralisation was monitored throughout. After 0, 3, 6, 12 and 16 months, samples were removed and analysed for chemical parameters and for microbial biomass. In addition, ¹⁴C activity measurements in bulk soil and microbial biomass were used to estimate their lignite content.Despite the high content of organic carbon in lignite-rich overburden material, low contents of microbial biomass were recorded. Ash-amelioration led to high pH values in the overburden material, resulting in high concentrations of dissolved organic carbon most likely derived from lignite. Development of the microbial community was subsequently stimulated by presence of an easily available carbon source. In older mine soils, larger amounts of microbial biomass are most likely related to the presence of recent organic matter. Radiocarbon analysis of the microbial biomass extracted from the 14-year-old mine soil indicated higher lignite carbon contribution than recorded for microbial biomass of the 37-year-old mine soil. The highest concentration of lignite C present in microbial biomass as indicated by the C_mic/C_org ratio was, however, observed in the ameliorated overburden material. Therefore, we conclude that the importance of lignite as a carbon source for micro-organisms decreases when recent organic matter is present in the older stages of mine soil development.     

Estimating the active and total soil microbial biomass by kinetic respiration analysis

 A model describing the respiration curves of glucose-amended soils was applied to the characterization of microbial biomass. Both lag and exponential growth phases were simulated. Fitted parameters were used for the determination of the growing and sustaining fractions of the microbial biomass as well as its specific growth rate (μ _max). These microbial biomass characteristics were measured periodically in a loamy silt and a sandy loam soil incubated under laboratory conditions. Less than 1% of the biomass oxidizing glucose was able to grow immediately due to the chronic starvation of the microbial populations in situ. Glucose applied at a rate of 0.5 mg C g^–1 increased that portion to 4–10%. Both soils showed similar dynamics with a peak in the growing biomass at day 3 after initial glucose amendment, while the total (sustaining plus growing) biomass was maximum at day 7. The microorganisms in the loamy silt soil showed a larger growth potential, with the growing biomass increasing 16-fold after glucose application compared to a sevenfold increase in the sandy loam soil. The results gained by the applied kinetic approach were compared to those obtained by the substrate-induced respiration (SIR) technique for soil microbial biomass estimation, and with results from a simple exponential model used to describe the growth response. SIR proved to be only suitable for soils that contain a sustaining microbial biomass and no growing microbial biomass. The exponential model was unsuitable for situations where a growing microbial biomass was associated with a sustaining biomass. The kinetic model tested in this study (Panikov and Sizova 1996) proved to describe all situations in a meaningful, quantitative and statistically reliable way. Received: 19 July 1999     

Microbial biomass and activities in partly hydromorphic agricultural and forest soils in the Bornhöved Lake region of Northern Germany

The soil microbial biomass and activity were estimated for seven field (intensive and extensive management), grassland (dry and wet), and forest (beech, dry and wet alder) sites. Three of the sites (wet grassland, dry and wet alder) are located on a lakeshore and are influenced by lake water and groundwater. Four different methods were selected to measure and characterize the microbial biomass. Values of microbial biomass (weight basis) and total microbial biomass per upper horizon and hectare (volume basis) were compared for each site.Fumigation-extraction and substrate-induced respiration results were correlated but dit not give the same absolute values for microbial biomass content. When using the original conversion factors, substrate-induced respiration gave higher values in field and dry grassland soils, and fumigation-extraction higher values in soils with low pH and high water levels (high organic content). Results from dimethylsulfoxide reduction and arginine ammonification, two methods for estimating microbial activity, were not correlated with microbial biomass values determined by fumigation-extraction or substrate-induced respiration in all soils examined. In alder forest soils dimethylsulfoxide reduction and arginine ammonification gave higher values on the wet site than on the dry site, contrary to the values estimated by fumigation-extraction and substrate-induced respiration. These microbial activities were correlated with microbial biomass values only in field and dry grassland soils. Based on soil dry weight, microbial biomass values increased in the order intensive field, beech forest, extensive field, dry grassland, alder forest, wet grassland. However, microbial biomass values per upper horizon and hectare (related to soil volume) increased in agricultural soils in the order intensive field, dry grassland, extensive field, wet grassland and in forest soils in the order beech, wet alder, dry alder. We conclude that use of the original conversion factors with the soils in the present study for fumigation-extraction and substrate-induced respiration measurements does not give the same values for the microbial biomass. Furthermore, dimethylsulfoxide reduction and arginine ammonification principally characterize specific microbial activities and can be correlated with microbial biomass values under specific soil conditions. Further improvements in microbial biomass estimates, particularly in waterlogged soils, may be obtained by direct counts of organisms, ATP estimate, and the use of ¹⁴C-labelled organic substrates. From the ecological viewpoint, data should also be expressed per horizon and hectare (related to soil volume) to assist in the comparison of different sites.     

Salinity reduces the ability of soil microbes to utilise cellulose

An incubation experiment was conducted to determine the response of soil microbial biomass and activity to salinity when supplied with two different carbon forms. One nonsaline and three saline soils of similar texture (sandy clay loam) with electrical conductivities of the saturation extract (EC_e) of 1, 11, 24 and 43 dS m^?1 were used. Carbon was added at 2.5 and 5 g C kg^?1 (2.5C, 5C) as glucose or cellulose; soluble N and P were added to achieve a C/N ratio of 20 and C/P ratio of 200. Soil microbial activity was assessed by measuring CO₂ evolution continuously for 3 weeks; microbial biomass C and available N and P were determined on days 2, 7, 14 and 21. In all soils, cumulative respiration was higher with 5C than with 2.5C and higher with glucose than with cellulose. Cumulative respiration was highest in the nonsaline soil and decreased with increasing EC, whereas the decrease was gradual with glucose, there was a sharp drop in cumulative respiration with cellulose from the nonsaline soil to soil with EC11 with little further decrease at higher ECs. Microbial biomass C and available N and P concentrations were highest in the nonsaline soil but did not differ among the saline soils. Microbial biomass C was higher and available N was lower with 5C than with 2.5C. The C form affected the temporal changes of microbial biomass and available nutrients differentially. With glucose, microbial biomass was highest on day 2 and then decreased, whereas available N showed the opposite pattern, being lowest on day 2 and then increasing. With cellulose, microbial biomass C increased gradually over time, and available N decreased gradually. It is concluded that salinity reduced the ability of microbes to decompose cellulose more than that of glucose.     

Determination and use of a corrected control factor in the chloroform fumigation method of estimating soil microbial biomass

Estimates of soil microbial biomass are important for both comparative system analysis and mechanistic models. The method for measuring microbial biomass that dominates the literature is the chloroform fumigation incubation method (CFIM), developed on the premise that killed microorganisms are readily mineralized to CO₂, which is a measure of the initial population. Factors that effect the CFIM have been thoroughly investigated over the last 15 years. A question that still remains after countless experiments is the use of an appropriate nonfumigated control for accounting for native soil organic matter (SOM) mineralization during incubation. Our approach was to add hot-water-leached ¹⁴C-labeled straw to both fumigated and nonfumigated samples assuming the straw would mimic a recalcitrant C substrate fraction of SOM. The ratio of the ¹⁴C evolved from the fumigated sample over the ¹⁴C evolved from the control sample would provide a corrected control value to be used in calculating microbial biomass. This experiment was conducted on soils from forest, agricultural, grassland and shrub-steppe ecosystems. The results clearly indicate that equal recalcitrant C mineralization during incubation is not a valid assumption. The results with these soils indicate than on the average only 20% of the control CO₂ should be subtracted from the fumigated CO₂ for the biomass calculation. The correction value ranged from 18% for agricultural soils to 25% for shrub-steppe soil, with the average correction value being 20%. Our experiments show that corrected biomass values will be 1.5–2 times greater than uncorrected biomass values. In addition using a corrected control improved the 1:1 correlation between the CFIM and SIR methods for these soils.     

PH对红壤微生物生物量碳和生物量磷的影响

The impact of pH changes on microbial biomass carbon (Cmic) and microbial biomass phosphorus (Pmic) were examined for 3 red soils under citrus production with different lengths of cultivation. Soil pH significantly affected Cmic and Pmic. The Cmie and Pmic changes, as a function of soil pH, appeared to follow a normal distribution with the original soil pH value at the apex and as pH increased or decreased compared to the original soil pH, Cmic and Pmic declined. Moreover, there were critical pH values at both extremes (3.0 on the acidic side and 8.0 to 8.5 on the alkaline side), beyond which most of microorganisms could never survive. The effect of pH on Cmic and Pmic was also related to the original soil pH. The higher the original soil pH was, the less Cmic or Pmic were affected by pH change. It is suggested that soil microorganisms that grow in a soil environment with a more neutral soil pH range (i.e. pH 5.5-7.5) may have a greater tolerance to pH changes than those growing in more acidic or more alkaline soil pH conditions.     

Nitrogen pools and turnover in arable soils under different durations of organic farming: I: Pool sizes of total soil nitrogen,microbial biomass nitrogen,and potentially mineralizable nitrogen

Soil organic matter contents, soil microbial biomass, potentially mineralizable nitrogen (N) and soil pH values were investigated in the Ap horizons of 14 field plots at 3 sites which had been under organic farming over various periods. The objective was to test how these soil properties change with the duration of organic farming. Site effects were significant for pH values, microbial biomass C and N, and for potentially mineralizable N at 0—10 cm depth. The contents of total organic C, total soil N, and potentially mineralizable N tended to be higher in soils after 41 versus 3 years of organic farming, but the differences were not significant. Microbial biomass C and N contents were higher after 41 years than after 3 years of organic farming at 0—10 cm depth, and the pH values were increased at 10—27 cm depth. Nine years of organic farming were insufficient to affect soil microbial biomass significantly. Increased biomass N contents help improve N storage by soil micro‐organisms in soils under long‐term organic farming.     

Mineralisation dans le sol de materiaux microbiens marques au carbone 14 et a l'azote 15: Quantification de l'azote de la biomasse microbienne

The mineralization of microbial material of different C-to-N ratios (5.2, 7.9, 10.2, 12.7) was followed in fumigated soil. The microbial materials used were from Aspergillus flavus cultures, grown in liquid media and labelled with [¹⁴C]glucose and (¹⁵NN4)3804. Three contrasting soils were used and the microbial materials incubated with the fumigated soils for 28 days at 28°C.The evolution of the added organic microbial C was fast: 80% of the [¹⁴C]CO₂ produced during the whole 28 days incubation was evolved in the first week. Microbial C mineralization was mainly related to soil type; the C-to-N ratio had small effect on the ratio (mineralized microbial carbon-to-added microbial carbon). Calculation of the K_c- coefficient (the fraction of the added microbial C mineralized in 7 days) shows that K_c values lie between 0.38 and 0.43 in the 3 soils.Organic N in the added microbial material also breaks down quickly: between 60 and 100% of the organic nitrogen mineralized was evolved during the first week of incubation. Mineralization kinetics are related to soil type and to the C-to-N ratio of the microbial material.The proportion of N mineralized in 7 days was lower in an acid soil than in near neutral soils and lower with high C-to-N ratio material than with low C-to-N ratio material. The ratio (mineralized microbial N-to-added microbial N) depends on soil type and is negatively correlated with the C-to-N ratio of the microbial material. The K_N value (the fraction of the added microbial N mineralized in 7 days) lies between 0.22 and 0.47 for the three soils and four materials investigated. The added microbial material induced a priming effect on soil native N: materials with C-to-N ratios of 10.2 and 12.7 produced negative priming effects whereas materials with C-to-N ratios of 5.2 and 7.9 sometimes produced a positive priming action.From the relationship between the C-to-N ratio of the added material and the (mineralized microbial C-to-mineralized microbial N) ratio, the soil native microbial biomass was estimated using the fiush-C-to-flush-N ratio. Biomass nitrogen was then calculated from the formula biomass-N = biomassC/(biomass C-to-N ratio). Calculated in this way, 2–4% of the total nitrogen in the three soils was in microbial biomass.