The spatial distribution of soil microbial biomass in a permanent row crop

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.     

Effect of residue placement and chemical fertilizer on soil microbial biomass under tropical dryland cultivation

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.     

Effect of cultivation on microbial carbon and nitrogen in dry tropical forest soil

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.     

Activity and biomass of soil microorganisms at different depths

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.     

Influence of soil properties on microbial C,N, and P in dry tropical ecosystems

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.     

Seasonal changes and the effects of fertiliser on some chemical,biochemical and microbiological characteristics of high-producing pastoral soil

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.     

Seasonal changes in microbial biomass and nutrient flush in forest soils

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.     

Application of the selective inhibition method to determine bacterial: fungal ratios in three beechwood soils rich in carbon — Optimization of inhibitor concentrations

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.     

Dynamics of soil biomass C,N, and P in a dry tropical forest in India

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.     

Microbial biomass and respiratory activity in soil aggregates of different sizes from three beechwood sites on a basalt hill

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 (A_h 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.     

Effects of nitrification inhibitors on denitrification of nitrate in soil

Summary The influence of 28 nitrification inhibitors on denitrification of nitrate in soil was studied by determining the effects of different amounts of each inhibitor on the amounts of nitrate lost and the amounts of nitrite, N₂O and N₂ produced when soil samples were incubated anaerobically after treatment with nitrate or with nitrate and mannitol. The inhibitors used included nitrapyrin (N-Serve), etridiazole (Dwell), potassium azide, 2-amino-4-chloro-6-methylpyrimidine (AM), sulfathiazole (ST), 4-amino-1,2,4-triazole(ATC),2,4-diamino-6-trichloromethyl-s-triazine (CL-1580), potassium ethylxanthate, guanylthiourea (ASU), 4-nitrobenzotrichloride, 4-mesylbenzotrichloride, sodium thiocarbonate (STC), phenylmercuric acetate (PMA), and dicyandiamide (DCD).Only one of the nitrification inhibitors studied (potassium azide) retarded denitrification when applied at the rate of 10 g g^–1 soil, and only two (potassium azide and 2,4-diamino-6-trichloromethyl-s-triazine) inhibited denitrification when applied at the rate of 50 g g^–1 soil. The other inhibitors either had no appreciable effect on denitrification, or enhanced denitrification, when applied at the rate of 10 or 50 g g^–1 soil, enhancement being most marked with 3-mercapto-1,2,4-triazole. Seven of the inhibitors (potassium azide, sulfathiazole, potassium ethylxanthate, sodium isopropylxanthate, 4-nitrobenzotrichloride, sodium thiocarbonate, and phenylmercuric acetate) retarded denitrification when applied at the rate of 50 g g^–1 soil to soil that had been amended with mannitol to promote microbial activity.Reports that nitrapyrin (N-Serve) and etridiazole (Dwell) inhibit denitrification when applied at rates as low as 0.5 g g^–1 soil could not be confirmed. No inhibition of denitrification was observed when these compounds were applied at the rate of 10 g g^–1 soil, and enhancement of denitrification was observed when they were applied at the rate of 50 or 100 g g^–1 soil.     

Effects of animal manure and mineral fertilizer on the total carbon and nitrogen contents of soil size fractions

Summary Soil was sampled in autumn 1984 in the 132 field (sandy loam soil) of the Askov long-term experiments (started in 1894) and fractionated according to particle size using ultrasonic dispersion and sedimentation in water. The unmanured plot and plots given equivalent amounts of N (1923–1984 annual average, 121 kg N/ha) in either animal manure or mineral fertilizer were sampled to a depth of 15 cm, fractionated and analysed for C and N. Mineral fertilizer and animal manure increased the C and N content of whole soil, clay (<2 m) and silt (2–20 m) size fractions relative to unmanured samples, while the C content of the sand size fractions (fine sand 1, 20–63 m; fine sand 2, 63–200 m; coarse sand, 200–2000 m) was less affected. Clay contained 58% and 65°70 of the soil C and N, respectively. Corresponding values for silt were 30% and 26%, while sand accounted for 10% of the soil C. Fertilization did not influence this distribution pattern. The C : N ratio of the silt organic matter (14.3) was higher and that of clay (10.6) lower than whole-soil C:N ratios (12.0). Fertilization did not influence clay and silt C : N ratios. Animal manure caused similar relative increases in the organic matter content of clay and silt size fractions (36%). In contrast, mineral fertilizer only increased the organic matter content of silt by 21% and that of clay by 14%.     

Interactions between 14C-labelled atrazine and the soil microbial biomass in relation to herbicide degradation

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.     

Suppression of methane oxidation in aerobic soil by nitrogen fertilizers,nitrification inhibitors,and urease inhibitors

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.     

Carbon and nitrogen dynamics in a phosphorus-deficient soil amended with organic residues and fertilizers in western Kenya

The contribution of organic resources to the restoration of soil fertility in smallholder farming systems in East Africa is being tested as an alternative to costly fertilizers. Organic inputs are expected to have advantages over fertilizers by affecting many biochemical properties controlling nutrient cycling. Our study examined changes in soil C and N, C and N mineralization, microbial biomass C (MBC) and N (MBN), and particulate organic matter (POM) in a P-limiting soil in western Kenya after applications of organic residues and fertilizers to overcome P limitation to crops. Leaf biomass from six different tree (shrub) species was incorporated into the soil at 5 Mg ha^–1 for five consecutive maize growing seasons, over 2.5 years. Triple superphosphate was applied separately at 0, 10, 25, 50, and 150 kg P ha^–1 in combination with 120 kg N ha^–1 as urea. Soil inorganic N, soil organic C, mineralizable N, and total C in all POM fractions and total N in the 53- to 250-m POM fraction increased following addition of all organic residues compared to the control. Whether there was an advantage of organic residue incorporation over inorganic fertilizer use depended on the soil parameter studied, the organic residue and the rate of fertilization. Most differences were found in N mineralization where 14.4–21.6 mg N kg^–1 was mineralized in fertilizer treatments compared to 25.2–30.5 mg N kg^–1 in organic residue treatments. C and N mineralization and the 53- to 250-m POM fractions were the most sensitive parameters, correlating with most of the studied parameters. Organic residues can contribute to improved soil nutrient cycling while the magnitude of their contribution depends on the biochemical properties of the residues.     

Nitrogen mineralization and reorganization in casts of the geophagous tropical earthworm Pontoscolex corethrurus (Glossoscolecidae)

Summary Mineral N concentrations ranged from 133.1 to 167.8 g g^-1 dry soil in fresh casts of the endogeic earthworm Pontoscolex corethrurus fed on an Amazonian Ultisol; this was approximately five times the concentration in non-ingested soil. Most of this N was in the form of NH _inf4 ^sup+ . N also accumulated in microbial biomass, which increased from a control value of 10.5–11.3 to 67.5–74.1 g g^-1 in fresh casts. During a 16-day incubation, part of the NH _inf4 ^sup+ -N was nitrified and/or transferred to the microbial biomass. Total labile N (i.e., mineral+biomas N) decreased sharply at first (ca. 50% in the first 12 h), and then more slowly. The exact fate of this N (microbial metabolites, denitrification, or volatilization) is not known. After 16 days, the overall N content of the casts was still 28% higher than that of the control soil. Incubation of the soil before ingestion by the earthworms significantly increased the production of NH _inf4 ^sup+ in casts. We calculate that in a humid tropical pasture, 50–100 kg mineral N may be produced annually in earthworm casts. Part of this N may be conserved in the compact structure of the cast where the cast is not in close contact with plant roots.     

Bioaccumulation of selenium by floating aquatic plants

The degree to which floating aquatic plants concentrate Se in tissues was determined for four species grown in solutions containing various levels of Se. Results of this greenhouse study showed that all four plant species, Azolla caroliniana, Eichhornia crassipes, Salvinia rotundi folia, and Lemna minor absorbed Se quickly upon exposure to Se in water as concentrated as 2.5 g Se mL^–1, and attained maximum tissue concentrations within 1 to 2 weeks. Azolla absorbed Se to the highest tissue concentration (about 1000 g Se g^–1 dry matter) from the 2.5 g Se mL^–1 solution, followed by Salvinia (700 g Se g^–1), Lemna (500 g Se g^–1),and Eichhornia (300 g Se g^–1). Plant growth appeared unaffected by solution Se concentrations lower than about 1.25 g mL^–1. These results indicate potential for rapid Se movement from water into aquatic food chains, and for use of aquatic plants for Se removal in wastewater treatment systems.     

Effect of the insecticide methidathion on agricultural soil microflora

Summary We studied the effects of the organophosphorus insecticide methidathion, at concentrations of 10, 50, 100, 200 and 300 g g^-1 in an agricultural soil, on fungi, total bacterial populations, aerobic N₂-fixing bacteria, denitrifying bacteria, nitrifying bacteria (phases I and II), and nitrogenase activity (acetylene reduction assay). The presence of 10–300 g g^-1 of methidathion significantly increased fungal populations (colony-forming units). Denitrifying bacteria, aerobic N₂-fixing bacteria and N₂ fixation were significantly increased at concentrations of 50–300 g g^-1. The total number of bacteria increased significantly at concentrations of 100–300 g g^-1. Nitrifying bacteria decreased initially at concentrations of 300 g g^-1, but recovered rapidly to levels similar to those in the control soil without the insecticide.     

Ergosterol and microbial biomass relationship in soil

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.     

Effects of crop growth and soil treatments on microbial C,N, and P in dry tropical arable land

We studied the dynamics of microbial C, N, and P in soil cropped with rice (Oryza sativa) and lentils (Lens culinaris) in a dryland farming system. The crop biomass and grain yield were also studied. The microbial biomass and its N and P contents were larger under the lentil than under the rice crop. Microbial nutrients decreased as the crops grew and then increased again. Farmyard manure and NPK fertilizer applications increased the level of microbial nutrients, crop biomass, and grain yield by 35–80%, 55–85%, and 74–86%, respectively. However, these applications had no significant effect on most of the soil physicochemical properties in the short term. The microbial biomass was correlated with the crop biomass and grain yield. The calculated flux of N and P through the microbial biomass ranged from 30–45 and 10–19 kg ha^-1 year^-1, respectively. Cultivation of a cereal crop followed by a leguminous crop sustains higher levels of microbial nutrients and hence greater fertility in impoverished tropical arable soils. The soil microbial biomass appears to contribute significantly to crop productivity by releasing nutrients, and applications of manure, either alone or with fertilizers, promote this effect more strongly than the application of NPK fertilizers alone.