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1.
Bacterial and fungal contributions to microbial respiration in three beechwood soils rich in C (two basalt soils and one limestone soil) were investigated by using streptomycin and cycloheximide to inhibit substrate-induced respiration after glucose (8000 g g-1), N, and P addition to soil samples. The inhibitors were added as solutions (2000, 8000, and 16000 g g-1) and the reduction in substrate-induced respiration after separate and combined inhibitor addition was measured in an automated electrolytic microrespirometer. Bacterial and fungal contributions to microbial respiration were calculated using the interval 6–10 h after inhibitor application. The microbial biomas was smaller in the two basalt soils (Oberhang and Mittelhang) than in the limestone soil (Unterhang). In the presence of both inhibitors, microbial respiration was inhibited by a maximum of 45, 45, and 25% in the two basalt soils and the limestone soil, respectively. Inhibition of microbial respiration was at a maximum at streptomycin and cycloheximide concentrations of 16000 g g-1. The inhibitor additivity ratio approached 1.0 even at high inhibitor concentrations, indicating high inhibitor selectivity. Calculated prokaryote: eukaryote ratios indicated lower bacterial contributions to the microbial biomass in the Mettelhang (0.74) and Unterhang (0.73) than in the Oberhang (0.88) soil.  相似文献   

2.
In February 1993 samples of litter from three different litter layers (upper, intermediate, and lower) were taken from a beechwood growing on basalt soil. Using the substrate-induced respiration method, we investigated the influence of fragmentation and glucose concentration on the maximum initial respiratory response. Glucose concentrations ranged between 0 and 160000 g g-1 dry weight. The initial respiratory response reached a maximum at 80000 g glucose g-1 dry weight. The addition of higher concentrations of glucose resulted in negligible changes in respiration. Litter materials of four different size classes (intact leaves, fragmented <100 mm2, <25 mm2, and <5 mm2) were amended with 80000 g glucose g-1 dry weight. Substrate-induced respiration was at a maximum in the size class <25 mm2. The addition of glucose to intact litter did not result in microbial growth. It is concluded that C is not the primary limiting element for the microflora in litter layers of the study site. Fragmentation of beech litter enabled the microorganisms to grow. Presumably, nutrients that limited microbial growth in intact litter were mobilized by the fragmentation procedure and enabled microorganisms to grow in fragmented litter materials.  相似文献   

3.
Seasonal changes in microbial biomass and nutrient flush in forest soils   总被引：14，自引：0，他引：14  
Microbial biomass and N, P, K, and Mg flushes were estimated in spring, summer, autumn, and winter samples of different forest soils. The microbial biomass showed significant seasonal fluctuations with an average distribution of 880±270 g C g-1 soil in spring, 787±356 g C g-1 soil in winter, 589±295 g C g-1 soil in summer, and 560±318 g C g-1 soil in autumn. The average annual concentrations of C, N, P, K, and Ca in the microbial biomass were 704, 106, 82, 69 and 10 g g-1 soil, respectively. Microbial C represented between 0.5 and 2% of the organic soil C whereas the percentage of microbial N with respect to the total soil N was two-to threefold higher than that of C; the annual fluctuations in these percentages followed a similar trend to that of the microbial biomass. Microbial biomass was positively correlated with soil pH, moisture, organic C, and total N. The mean nutrient flush was 31, 15, 7, and 4 g g-1 soil for N, K, P, and Mg, respectively, and except for K, the seasonal distribution was autumn spring winter summer. The average increase in available nutrient due to the mineralization of dead microbial cells was 240% for N, and 30, 26, and 14% for P, K, and Mg, respectively. There was a positive relationship between microbial biomass and the N, P, K, and Mg flushes. All the variables studied were significantly affected by the season, the type of soil, and the interaction between type of soil and season, but soil type often explained most of the variance.  相似文献   

4.
Summary Relationships between soil physicochemical characteristics and soil microbial C, N, and P in Indian dry tropical ecosystems are discussed. The major ecosystem studies were on forest, savanna, cropped fields, and mine spoils. The highest microbial C, N, and P levels were recorded from the mixed forest and the lowest levels in 5-year-old mine spoil. Across the sites, microbial C ranged from 226 to 643 g g-1, microbial N from 19 to 71 g g-1, and microbial P from 9 to 28 g g-1 soil. The proportion of soil organic C contained in the microbial biomass ranged from 2.2 to 5.0%. The microbial C: N ratio in these soils ranged from 7.4. to 13.1 and the microbial C: P ratio from 16.6 to 30.6. The concentrations of microbial C, N, and P were correlated with several soil properties and among themselves. The soil properties, in various linear combinations, explained 90–99% of the variability in the microbial nutrients. Grazing of the savanna had some effect on the level of microbial biomass, and as the mine spoil aged, the level of microbial C, N, and P also increased.  相似文献   

5.
We studied the effects of aggregates of different sizes on the soil microbial biomass. The distribution of aggregate size classes (<2, 2–4, 4–10, >10 mm) in the upper mineral soil horizon (Ah layer) was very different in three sites (upper, intermediate, lower) in a beechwood (Fagus sylvatica) on a basalt hill (Germany). Aggregates of different sizes (<2, 2–4, 4–10 mm) contained different amounts of C and N but the C:N ratios were similar. C and N contents were generally higher in smaller aggregates. The maximum initial respiratory response by microorganisms in intact aggregates and in aggregates passed through a 1-mm sieve declined with the aggregate size, but the difference was more pronounced in intact aggregates. Disruption of aggregates generally increased this response, particularly in 4- to 10-mm aggregates in the lower site. Basal respiration differed strongly among sites, but was similar in each of the aggregate size classes. Aggregate size did not significantly affect the specific respiration (g O2 g–1 microbial C h–1) nor the microbial: organic C ratio, but these parameters differed among sites. Microbial growth was increased strongly by passing the soil through a 1-mm sieve in each of the aggregate materials. The growth of microorganisms in disrupted aggregates was similar, and the effect of aggregate disruption depended on the growth of microorganisms in intact aggregates.  相似文献   

6.
We studied the reactions of humus layer (F/H) microbial respiratory activity, microbial biomass C, and the fungal biomass, measured as the soil ergosterol content, to the application of three levels of wood ash (1000, 2500, and 5000 kg ha-1) and to fire treatment in a Scots pine (Pinus sylvestris L.) stand. Physicochemical measurements (pH, organic matter content, extractable and total C content, NH 4 + and total N content, cation-exchange capacity, base saturation) showed similarity between the fire-treated plots and those treated with the lowest dose of wood ash (1000 kg ha-1). The ash application did not change the level of microbial biomass C or fungal ergosterol when compared to the control, being around 7500 and 350 g g-1 organic matter for the biomass C and ergosterol, respectively. The fire treatment lowered the values of both biomass measurements to about half that of the control values. The fire treatment caused a sevenfold fall in the respiration rate of fieldmoist soil to 1.8 l h-1 g-1 organic matter compared to the values of the control or ash treatments. However, in the same soils adjusted to a water-holding capacity of 60%, the differences between the fire treatment and the control were diminished, and the ash-fertilized plots were characterized by a higher respiration rate compared to the control plots. The glucose-induced respiration reacted in the same way as the water-adjusted soil respiration. The metabolic quotient, qCO2, gradually increased from the control level with increasing applications of ash, reaching a maximum in the fire treatment. Nitrification was not observed in the treatment plots.  相似文献   

7.
Soils from 38 German forest sites, dominated by beech trees (Fagus sylvatica L.) were sampled to a depth of about 10 cm after careful removal of overlying organic layers. Microbial biomass N and C were measured by fumigation-extraction. The pH of the soils varied between 3.5 and 8.3, covering a wide range of cation exchange capacity, organic C, total N, and soil C:N values. Maximum biomass C and biomass N contents were 2116 g C m-2 and 347 g N m-2, while minimum contents were 317 and 30 g m-2, respectively. Microbial biomass N and C were closely correlated. Large variations in microbial biomass C:N ratios were observed (between 5.4 and 17.3, mean 7.7), indicating that no simple relationship exists between these two parameters. The frequency distribution of the parameters for C and N availability to the microflora divided the soils into two subgroups (with the exception of one soil): (1) microbial: organic C>12 mg g-1, microbial:total N>28 mg g-1 (n=23), a group with high C and N availability, and (2) microbial:organic C12 mg g-1, microbial:total N28 mg g-1 (n=14), a group with low C and N availability. With the exception of a periodically waterlogged soil, the pH of all soils belonging to subgroup 2 was below 5.0 and the soil C:N ratios were comparatively high. Within these two subgroups no significant correlation between the microbial C:N ratio and soil pH or any other parameter measured was found. The data suggest that above a certain threshold (pH 5.0) microbial C:N values vary within a very small range over a wide range of pH values. Below this threshold, in contrast, the range of microbial C:N values becomes very large.  相似文献   

8.
A laboratory incubation experiment was set up to determine the effects of atrazine herbicide on the size and activity of the soil microbial biomass. This experiment was of a factorial design (0, 5, and 50 g g–1 soil of non-labelled atrazine and 6.6×103 Bq g–1 soil of 14C-labelled atrazine) x (0, 20, and 100 g g–1 soil of urea-N) x (pasture or arable soil with a previous history of atrazine application). Microbial biomass, measured by substrate-induced respiration and the fumigation-incubation method, basal respiration, incorporation of 14C into the microbial biomass, degradation of atrazine, and 14C remaining in soil were monitored over 81 days. The amount of microbial biomass was unaffected by atrazine although atrazine caused a significant enhancement of CO2 release in the non-fumigated controls. Generally, the amounts of atrazine incorporated into the microbial biomass were negligible, indicating that microbial incorporation of C from atrazine is not an important mechanism of herbicide breakdown. Depending on the type of soil and the rate of atrazine application, 18–65% of atrazine was degraded by the end of the experiment. Although the pasture soil had twice the amount of microbial biomass as the arable soil, and the addition of urea approximately doubled the microbial biomass, this did not significantly enhance the degradation of atrazine. This suggests that degradation of atrazine is largely independent of the size of the microbial biomass and suggests that other factors (e.g., solubility, chemical hydrolysis) regulate atrazine breakdown. A separate experiment conducted to determine total amounts of 14C-labelled atrazine converted into CO2 by pasture and arable soils showed that less than 25% of the added 14C-labelled atrazine was oxidised to 14CO2 during a 15-week period. The rate of degradation was significantly greater in the arable soil at 24%, compared to 18% in the pasture soil. This indicates that soil microbes with previous exposure to atrazine can degrade the applied atrazine at a faster rate.  相似文献   

9.
Changes in the soil microbial biomass following applications of farmyard manure and inorganic fertilizer, alone and in combination, were studied for two annual cycles in a rice-lentil crop sequence grown under rainfed tropical dryland conditions. During the two annual cycles the microbial biomass C range (g g-1) was 146–241 (x = 204), 191–301 (245), 244–382 (305), and 294–440 (365) in control, fertilizer, manure and manure+fertilizer plots, respectively. The corresponding ranges for microbial biomass N (g g-1) were 16.5–21.0 (19.5), 20.4–38.2 (26.0), 23.0–34.6 (27.0) and 26.2–42.4 (33.3), and for microbial biomass P (g g-1) 4.4–8.2 (7.0) 6.0–11.2 (9.6), 11.2–22.0 (17.0), and 10.0–25.4 (18.3). The maximum increase in the microbial biomass, due to these inputs was observed under the manure+fertilizer treatment followed, in decreasing order, by manure alone and fertilizer alone. Within individual crop periods the levels of microbial biomass decreased sharply from the seedling to the flowering stage and then increased slightly with crop maturity. The maximum levels of microbial biomass C and P were observed during the summer fallow. The maximum accumulation of microbial biomass N occurred in the early rainy season, immediately after the soil amendments. Microbial biomass C, N, and P were positively related to each other throughout the annual cycle.  相似文献   

10.
Ergosterol and microbial biomass C were measured in 26 arable, 16 grassland and 30 forest soils. The ergosterol content ranged from 0.75 to 12.94 g g-1 soil. The geometric mean ergosterol content of grassland and forest soils was around 5.5 g g-1, that of the arable soils 2.14 g g-1. The ergosterol was significantly correlated with biomass C in the entire group of soils, but not in the subgroups of grassland and forest soils. The geometric mean of the ergosterol: microbial biomass C ratio was 6.0 mg g-1, increasing in the order grassland (5.1), arable land (5.4) and woodland (7.2). The ergosterol:microbial biomass C ratio had a strong negative relationship with the decreasing cation exchange capacity and soil pH, indicating that the fungal part of the total microbial biomass in soils increased when the buffer capacity decreased. The average ergosterol concentration calculated from literature data was 5.1 mg g-1 fungal dry weight. Assuming that fungi contain 46% C, the conversion factor from micrograms ergosterol to micrograms fungal biomass C is 90. For soil samples, neither saponification of the extract nor the more effective direct saponification during extraction seems to be really necessary.  相似文献   

11.
Summary A 2-year study (1983–1984 to 1984–1985) was conducted to estimate temporal and seasonal changes and the effects of fertiliser on some soil chemical, biochemical and microbiological characteristics. The soil used was a Typic Vitrandept under grazed pasture. Soil samples were taken regularly to a depth of 75 mm from paired unfertilised and fertilised (500 kg ha– 30% potassic superphosphate) plots. Except for organic C, fertiliser had little or no effect on the characteristics measured. Organic C averaged about 9.2% in unfertilised soil and was about 0.3% higher in the fertilised soil. The size of the microbial biomass fluctuated widely in the 1st year (3000 g C g–1 in February to 1300 g C g–1 in September) but there was less variation in the 2nd year (range 1900 g C g–1 to 2500 g C g–1 soil). CO2 production values (10- to 20-day estimates averaged 600 g of CO2-C g–1 soil) were generally higher in spring compared to the rest of the year. Water extractable C increased over winter and declined through spring in both years (range 50 g C g–1 soil to 150 g C g–1 soil). Mineral-N flush values were higher in summer (300 g N g–1 soil) and lower in winter months (200 g N g–1 soil). The pattern of variation of microbial N values was one of gradual accumulation followed by rapid decline. This rapid decline in values occurred in spring and autumn (range 130–220 g N g–1 soil). N mineralisation and bicarbonate-extractable N showed no clear trend; these values ranged from 100–200 and 122–190 g N g–1 soil, respectively. There was a significant correlation (0.1%) between N mineralisation and bicarbonate-extractable N in the late summer-autumn-early winter period (February–August) in both years but not in spring. These results and their relationships to climatic factors and rates of pasture production are discussed.  相似文献   

12.
Dynamics of soil biomass C,N, and P in a dry tropical forest in India   总被引：6，自引：0，他引：6  
Summary Three dry tropical forest soils along a topographic sequence were examined to determine the seasonal dynamics of microbial C, N, and P. The lowest microbial biomass was found in forest soils at the foot of the hill followed by midslope forest soils. The hilltop soil, which had the most fine particles, water-holding capacity, organic C, and total N, reflected the presence of greater amounts of microbial C, N, and P. Mean annual microbial C, N, and P ranges were 466–662, 48–72 to 21–30 g g-1, respectively. The seasonal pattern of microbial biomass, C, N, and P was similar at all sites, the values being greatest during the dry season and lowest during the wet season. The seasonal values for microbial biomass C, N, and P were positively correlated with each other and a negative correlation was found between microbial biomass and the fine root mass in these forest soils.  相似文献   

13.
The effects of soil texture (silt loam or sandy loam) and cultivation practice (green manure) on the size and spatial distribution of the microbial biomass and its metabolic quotient were investigated in soils planted with a permanent row crop of hops (Humulus lupulus). The soil both between and in the plant rows was sampled at three different depths (0–10, 10–20, and 20–30 cm). The silt loam had a higher overall microbial biomass C concentration (260 g g-1) than the sandy loam (185 g g-1), whereas the sandy loam had a higher (3.1 g CO2-C mg-1 microbial Ch-1) metabolic quotient than the silt loam (2.6 g CO2-C mg-1 microbial C h-1), on average over depth (0–30 cm) and over all treatments. There was a sharp decrease in the microbial biomass with increasing depth for all plots. However, this was more pronounced in the silt loam than in the sandy loam. There was no distinct influence of sampling depth on the metabolic quotient. The microbial biomass was considerably higher in the rows than between the rows, especially in the silt loam plots. There was no significant difference between plots without green manure and plots with green manure for either the microbial biomass or the metabolic quotient.  相似文献   

14.
Summary Increasing the sulfate concentration and concomitant increases in the organic S concentration failed to exert any effect on organic S mobilization in samples collected from all depths within the mineral soil profile, from 15 sites differing in soil type, vegetation, and geographic location. Mobilization capacities at saturating concentrations of sulfate for organic S formation generally tended to increase with increasing depth. The potentials for the accumulation of organic S with various sulfate inputs exhibited saturation kinetics similar to those observed for organic S formation; values for the former parameter ranged from 3×10-3 to 12.6 mol S g–1 dry weight 24 h-1 for the uppermost (A, E) soil horizons, 3 nmol to 10 mol S g-1 dry weight 24 h–1 for intermediate (primarily AB) soil horizons, and from 3 nmol to 13.4 mol S g-1 dry weight 24 h–1 for the lowermost (B, C) soil horizons. Irrespective of depth, the Fullerton, Tarklin, and Loblolly sites in Tennessee and the Florida site showed the least net accumulation of organic S at saturation (<0.2 mol S g-1 dry weight 24 h–1 for all horizons examined), while the Duke Forest (North Carolina), Douglas Fir (Washington), Whiteface (New York) and the Howland (Maine) sites had the highest potential net accumulation of organic S at saturation (>1.0 mol S g-1 dry weight 24 h-1 for most horizons examined).  相似文献   

15.
Four treatments (control, chemical fertilizer, wheat straw, and wheat straw+fertilizer) were established on the dryland experimental farm of the Institute of Agricultural Sciences, Banaras Hindu University. Organic in C in the different treatments ranged from 0.69 to 0.93%, total N from 0.08 to 0.11%, and total P from 0.018 to 0.021. The application of straw significantly increased the soil water-holding capacity. The maximum effect on the microbial biomass was realized with the straw+fertilizer treatment, followed by straw and then by the fertilizer treatment. During the study microbial biomass C ranged from 144 to 491 g g-1 dry soil, biomass N from 14.6 to 50.1 g g-1, and biomass P from 7.2 to 17.6 g g-1 soil. Microbial biomass C, N and P represented 3.2–4.6% of total C, 2.6–3.8% of total N, and 5.8–8.2% of total P in the soil, respectively, in all cases the highest proportion occurred in the straw+fertilizer treatment and the lowest in the control. Microbial biomass C, N, and P were positively correlated with each other. Microbial biomass C and N increased by 77% in straw+fertilizer-treated plots relative to the control. The increase in microbial biomass P in the straw+fertilizer treatment over the control was 81%. The increase in the microbial biomass is expected to enhance nutrient availability in the soil, as the microbial biomass acts both as a sink and a source of plant nutrients.  相似文献   

16.
We measured microbial biomass C and soil organic C in soils from one grassland and two arable sites at depths of between 0 and 90 cm. The microbial biomass C content decreased from a maximum of 1147 (0–10 cm layer) to 24 g g-1 soil (70–90 cm layer) at the grassland site, from 178 (acidic site) and 264 g g-1 soil (neutral site) at 10–20 cm to values of between 13 and 12 g g-1 soil (70–90 cm layer) at the two arable sites. No significant depth gradient was observed within the plough layer (0–30 cm depth) for biomass C and soil organic C contents. In general, the microbial biomass C to soil organic C ratio decreased with depth from a maximum of between 1.4 and 2.6% to a minimum of between 0.5 and 0.7% at 70–90 cm in the three soils. Over a 24-week incubation period at 25°C, we examined the survival of microbial biomass in our three soils at depths of between 0 and 90 cm without external substrate. At the end of the incubation experiment, the contents of microbial biomass C at 0–30 cm were significantly lower than the initial values. At depths of between 30 and 90 cm, the microbial biomass C content showed no significant decline in any of the four soils and remained constant up to the end of the experiment. On average, 5.8% of soil organic C was mineralized at 0–30 cm in the three soils and 4.8% at 30–90 cm. Generally, the metabolic quotient qCO2 values increased with depth and were especially large at 70–90 cm in depth.  相似文献   

17.
Microbial biomass phosphorus in soils of beech (Fagus sylvatica L.) forests   总被引：3，自引：0，他引：3  
Thirty-eight soils from forest sites in central Germany dominated by beech trees (Fagus sylvatica L.) were sampled to a depth of about 10 cm after careful removal of the overlying organic layers. Microbial biomass P was estimated by the fumigation — extraction method, measuring the increase in NaHCO3-extractable phosphate. The size of the microbial P pool varied between 17.7 and 174.3 g P g-1 soil and was on average more than seven times larger than NaHCO3-extractable phosphate. Microbial P was positively correlated with soil organic C and total P, reflecting the importance of soil organic matter as a P source. The mean microbial P concentration was 13.1% of total P, varying in most soils between 6 and 18. Microbial P and microbial C were significantly correlated with each other and had a mean ratio of 14.3. A wide (5.1–26.3) microbial C: P ratio indicates that there is no simple relatinship between these two parameters. The microbial C: P ratio showed strong and positive correlations with soil pH and cation exchange capacity.  相似文献   

18.
Four contrasting soils were amended with glucose at concentrations up to 10 mg g?1 soil. The soils were incubated at 22°C for 14 days and the biomass determined at various times by chloroform fumigation or substrate-induced respiration. The adenosine triphosphate (ATP) content or the amylase and dehydrogenase activities were also determined. The size of the increases in biomass, ATP content and the enzyme activities was generally related to the amount of glucose added. The initially higher ATP levels quickly declined, and apparent substrate conversion figures up to 84% indicated that substrate-induced respiration overestimated the biomass. There were generally no significant correlations between ATP, biomass or enzyme activities.  相似文献   

19.
Summary Fifteen- and forty-year-old cropfields developed from a dry tropical forest were examined for soil organic C and total N and soil microbial C and N. The 15-year-old field had never been manured while the 40-year-old field had been fertilized with farmyard manure every year. The native forest soil was also examined. The results indicated that the native forest soil lost about 57% and 62% organic C and total N, respectively, in the 0–10 cm layer after 15 years of cultivation. The microbial C and N contents of the forest soil were greater than those of the cultivated soils. Application of farmyard manure increased the biomass-C and -N levels in the cultivated soil but the values were still markedly lower than in the forest soil. There was an appreciable seasonal variation in biomass C and N, the values being highest in summer and lowest in the rainy season. During an annual cycle, biomass-C contents varied from 180 to 727 g g–1 and N from 20 to 80 g g–1 dry soil, and both were linearly related. Microbial biomass C represented 1.6%–3.6% of total soil organic C and microbial biomass N represented 1.7% 1–4.4% of soil organic N.  相似文献   

20.
Concentrations of CH4, a potent greenhouse gas, have been increasing in the atmosphere at the rate of 1% per year. The objective of these laboratory studies was to measure the effect of different forms of inorganic N and various N-transformation inhibitors on CH4 oxidation in soil. NH 4 + oxidation was also measured in the presence of the inhibitors to determine whether they had differential activity with respect to CH4 and NH 4 + oxidation. The addition of NH4Cl at 25 g N g-1 soil strongly inhibited (78–89%) CH4 oxidation in the surface layer (0–15 cm) of a fine sandy loam and a sandy clay loam (native shortgrass prairie soils). The nitrification inhibitor nitrapyrin (5 g g-1 soil) inhibited CH4 oxidation as effectively as did NH4Cl in the fine sandy loam (82–89%), but less effectively in the sandy clay loam (52–66%). Acetylene (5 mol mol-1 in soil headspace) had a strong (76–100%) inhibitory effect on CH4 consumption in both soils. The phosphoroamide (urease inhibitor) N-(n-butyl) thiophosphoric triamide (NBPT) showed strong inhibition of CH4 consumption at 25 g g-1 soil in the fine sandy loam (83%) in the sandy clay loam (60%), but NH 4 + oxidation inhibition was weak in both soils (13–17%). The discovery that the urease inhibitor NBPT inhibits CH4 oxidation was unexpected, and the mechanism involved is unknown.  相似文献   

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