Spatial patterns of soil biological and physical properties in a ridge tilled and a ploughed Luvisol

The present study was conducted to determine the spatial heterogeneity of bulk density, soil moisture, inorganic N, microbial biomass C, and microbial biomass N in the ridge tillage system of Turiel compared to conventional mouldboard ploughing on three sampling dates in May, July, and August. The soil sampling was carried out under vegetation representing the ridge in a high spatial resolution down the soil profile. Bulk density increased with depth and ranged from 1.3 g cm⁻³ at 10 cm depth to 1.6 g cm⁻³ at 35 cm in ploughed plots and from 1.0 g m⁻³ at 5 cm to 1.4 g m⁻³ at 35 cm in the ridges. In the ploughed plots, the contents of microbial biomass C and microbial biomass N remained roughly constant at 215 and 33 μg g⁻¹ soil, respectively, throughout the experimental period. The microbial biomass C/N ratio varied in a small range around 6.4. In the ridged plots, the contents of microbial biomass C and microbial biomass N were 5% and 6% higher compared to the ploughed plots. Highest microbial biomass C contents of roughly 300 μg g⁻¹ soil were always measured in the crowns in July. The lowest contents of microbial biomass C of 85–137 μg g⁻¹ soil were measured in the furrows. The ridges showed strong spatial heterogeneity in bulk density, soil water content, inorganic nitrogen and microbial biomass.     

Changes in microbial community structure in soil as a result of different amounts of nitrogen fertilization

The changes in size, activity and structure of soil microbial community caused by N fertilization were studied in a laboratory incubation experiment. The rates of N fertiliser applied (KNO₃) were 0 (control), 100 and 2,000 μg N g⁻¹ soil. Despite no extra C sources added, a high percentage of N was immobilized. Whereas no significant increase of microbial C was revealed during incubation period, microbial growth kinetics as determined by the substrate-induced growth-response method demonstrated a significant decrease in the specific growth rate of microbial community in soil treated with 2,000 μg N g⁻¹ soil. Additionally, a shift in microbial community structure resulting in an increase in fungal biomarkers, mainly in the treatment with 2,000 μg N g⁻¹ soil was visible.     

Soil‐microbial response to sugarcane filter cake and biogenic waste compost

An incubation experiment was carried out to examine the N‐immobilizing effect of sugarcane filter cake (C : N = 12.4) and to prove whether mixing it with compost (C : N = 10.5) has any synergistic effects on C and N mineralization after incorporation into the soil. Approximately 19% of the compost‐C added and 37% of the filter cake–C were evolved as CO₂, assuming that the amendments had no effects on the decomposition of soil organic C. However, only 28% of the added filter cake was lost according to the total‐C and δ¹³C values. Filter cake and compost contained initially significant concentrations of inorganic N, which was nearly completely immobilized between day 7 and 14 of the incubation in most cases. After day 14, N remineralization occurred at an average rate of 0.73 µg N (g soil)^–1 d^–1 in most amendment treatments, paralleling the N mineralization rate of the nonamended control without significant difference. No significant net N mineralization from the amendment N occurred in any of the amendment treatments in comparison to the control. The addition of compost and filter cake resulted in a linear increase in microbial biomass C with increasing amounts of C added. This increase was not affected by differences in substrate quality, especially the three times larger content of K₂SO₄‐extractable organic C in the sugarcane filter cake. In most amendment treatments, microbial biomass C and biomass N increased until the end of the incubation. No synergistic effects could be observed in the mixture treatments of compost and sugarcane filter cake.     

Critical sulphur concentration and sulphur requirement of microbial biomass in a glucose and cellulose-amended regosol

 The critical S concentration and S requirement of the soil microbial biomass of a granitic regosol was examined. S was applied at the rate of 0, 5, 10, 20, 30 and 50 μg S as MgSO₄·7H₂O, together with either 3000 μg glucose-C or 3333 μg cellulose-C, 400 μg N, and 200 μg P g ^–1 soil and 200 μg K g^–1 soil. Microbial biomass, inorganic SO₄ ^2–-S, and CO₂ emission were monitored over 30 days during incubation at 25  °C. Both glucose and cellulose decomposition rates responded positively to the S made available for microbial cell synthesis. The amounts of microbial biomass C and S increased with the level of applied S up to 10 μg S g^–1 soil and 30 μg S g^–1 soil in the glucose- and cellulose-amended soil, respectively, and then declined. Incorporated S was found to be concentrated within the microbial biomass or partially transformed into soil organic matter. The concentration of S in the microbial biomass was higher in the cellulose- (4.8–14.2 mg g^–1) than in the glucose-amended soil (3.7–10.9 mg g^–1). The microbial biomass C:S ratio was higher in the glucose- (46–142 : 1) than in the cellulose-amended soil (36–115 : 1). The critical S concentration in the microbial biomass (defined as that required to achieve 80% of the maximum synthesis of microbial biomass C) was estimated to be 5.1 mg g^–1 in the glucose- and 10.9 mg g^–1 in the cellulose-amended soil. The minimum requirement of SO₄ ^2–-S for microbial biomass formation was estimated to be 11 μg S g^–1 soil and 21 μg S g^–1 soil for glucose- and cellulose-amended soil, respectively. The highest levels of activity of the microbial biomass were observed at the SO₄ ^2–-S concentrations of 14 μg S g^–1 soil and 17 μg S g^–1 soil, for the glucose and cellulose amendments, respectively, and were approximately 31–54% higher during glucose than cellulose decomposition. Received: 20 October 1999     

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     

Soil chemical and microbiological properties in hay production systems: residual effects of contrasting N fertilization of swine lagoon effluent versus ammonium nitrate

This study characterized soil chemical and microbiological properties in hay production systems that received from 0 to 600 kg plant-available N (PAN) ha⁻¹ year⁻¹ from either swine lagoon effluent (SLE) or ammonium nitrate (AN) from 1999 to 2001. The forage systems contained plots planted with bermudagrass (Cynodon dactylon L.) or endophyte-free tall fescue (Festuca arundinaceae Schreb.). In March 2004, the plots were sampled for measurements of a suite of soil chemical and microbiological properties. Nitrogen fertilization rates were significantly correlated with soil pH and K₂SO₄-extractable soil C but not with total soil C, soil C/N ratio, electrical conductivity, or Mehlich-3-extractable nutrients. Soil supplied with SLE had significantly lower Mehlich-3-extractable nutrients than the soil supplied with AN. Two indicators of soil N-supplying capacity (potentially mineralizable N and amino sugar N) varied with plant species and the type of N fertilizer. However, they generally peaked at an application rate of 200 or 400 kg PAN ha⁻¹ year⁻¹. Soil microbial biomass C also peaked at an application rate of 200 or 400 kg PAN ha⁻¹ year⁻¹. Nitrification potential was significantly higher in soil supplied with AN than in the unfertilized control but was similar between SLE-fertilized and unfertilized soils. Our results indicated that an application rate as high as 600 kg PAN ha⁻¹ year⁻¹ did not benefit soil microbial biomass, microbial activity, and N transformation processes in these forage systems.     

Short-term decomposition of <Superscript>14</Superscript>C-labelled glucose in a fluvo-aquic soil as affected by lanthanum amendment

In this study, we investigated the effects of lanthanum (La), one of the rare earth elements (REEs), on microbial biomass C as well as the decomposition of ¹⁴C-labelled glucose in a fluvo-aquic soil in 28 days. The soil was collected from the field plots under maize/wheat rotation in Fengqiu Ecological Experimental Station of Chinese Academy of Sciences, Henan Province, China. Application of La decreased soil microbial biomass C during the experimental period, and there was a negative correlation (P < 0.01) between microbial biomass and application rate of La. La increased microbial biomass ¹⁴C after ¹⁴C glucose addition, and the increase was significant (P < 0.05) at the rates of more than 160 mg kg⁻¹ soil. La slightly increased ¹⁴CO₂ evolution at lower rates of application but decreased it at higher rates 1 day after ¹⁴C glucose addition, while there was no significant effect from days 2 to 28. For the cumulative ¹⁴CO₂ evolution during the incubation of 28 days, La slightly increased it at the rates of less than 120 mg kg⁻¹ soil, while significantly decreased (P < 0.05) it at the rate of 200 mg kg⁻¹ soil. The results indicated that agricultural use of REEs such as La in soil could decrease the amount of soil microbial biomass and change the pattern of microbial utilization on glucose C source in a short period.     

Comparison of the difference method and 15N technique for studying the fate of nitrogen from plant residues in soil

We compared the dynamics of net mineralization of nitrogen (N) derived from white clover material (Ndfc) as measured by the difference and the ¹⁵N methods in a pot experiment with a sandy loam (15°C and pF 2.4) planted with Italian ryegrass. On day 22, mineralized Ndfc (soil mineral N plus plant N uptake) was 5.8% and 1.3% of added N for the ¹⁵N and the difference methods, respectively. The discrepancy was reduced on day 43. On day 64, the relationship was reversed, and on day 98 the values given by the two methods were 22.8% and 29.5%, respectively. The results obtained by the two methods were linearly correlated (r = 0.987) and, on average, did not differ significantly. Nevertheless, the different temporal patterns led to appreciably different parameter values as estimated by fitting of a reparameterized Richards model. On day 22, clover amendment reduced mineralized N derived from soil (Ndfs) by 3.4 mg N pot^–1. The reason for this was that the clover amendment led to a reduction in plant growth and uptake of Ndfs, most likely because of allelopathy, while mineral Ndfs did not increase correspondingly. Clover-induced Ndfs in the microbial biomass of 5.1 mg N pot^–1 suggested that the mineral Ndfs not taken up by plants had been reimmobilized. Towards the end of the experiment, clover-induced Ndfs in the biomass declined to 1.5 mg N pot^–1, while mineralized Ndfs due to clover amendment increased to 5.1 mg N pot^–1. The results strongly suggested that this increase was caused by a real stimulation of humus N mineralization by clover amendment rather than by isotope displacement or pool substitution. Received: 5 May 1997     

Vineyard soils under organic and conventional management—microbial biomass and activity indices and their relation to soil chemical properties

Eight vineyards in Pfaffenheim (P) and Turckheim (T) close to Colmar, France, forming four pairs of organic and conventional vineyards, were analyzed for microbial biomass and activity indices in relation to important soil chemical properties (carbon, nutrient elements, heavy metals) and also to differences between the bottom and top positions on the vineyard slope. The question was whether the vineyard management affects especially the soil microbiological indices. Three locations were on limestone (P-I, P-II, T-II), one on granite (T-I). The gravel content (>2 mm) ranged from 9 to 47%. The management systems had no significant main effect on the contents of organic C, total N, P, and S. The mean total contents of man-derived heavy metals decreased in the order Cu (164 μg g⁻¹ soil) > Zn (100 μg g⁻¹ soil) > Pb (32 μg g⁻¹ soil). The contents of microbial biomass C varied between 320 and 1,000 μg g⁻¹ soil. The significantly highest content was found at location P-II, the significantly lowest at the moderately acidic location T-I. The contents of microbial biomass N and adenosine triphosphate showed a similar trend. At location T-I, the fungal ergosterol-to-microbial biomass C ratio and the metabolic quotient qCO₂ were significantly highest, whereas the percentage of soil organic C present as microbial biomass C was lowest. Highest percentages of soil organic C present as microbial biomass C and lowest qCO₂ values were found in the organic in comparison with the conventional vineyards. None of the soil microbiological indices was significantly affected by the position on the slope, but all were significantly affected by the management system. This was mainly due to the highest index levels in the organic vineyard location P-II with the longest history in organic management.     

Influence of soil phosphorus status and nitrogen addition on carbon mineralization from 14C-labelled glucose in pasture soils

 This study examines the effect of soil P status and N addition on the decomposition of ¹⁴C-labelled glucose to assess the consequences of reduced fertilizer inputs on the functioning of pastoral systems. A contrast in soil P fertility was obtained by selecting two hill pasture soils with different fertilizer history. At the two selected sites, representing low (LF) and high (HF) fertility status, total P concentrations were 640 and 820 mg kg^–1 and annual pasture production was 4,868 and 14,120 kg DM ha^–1 respectively. Soils were amended with ¹⁴C-labelled glucose (2,076 mg C kg^–1 soil), with and without the addition of N (207 mg kg^–1 soil), and incubated for 168 days. During incubation, the amounts of ¹⁴CO₂ respired, microbial biomass C and ¹⁴C, microbial biomass P, extractable inorganic P (P_i) and net N mineralization were determined periodically. Carbon turnover was greatly influenced by nutrient P availability. The amount of glucose-derived ¹⁴CO₂ production was high (72%) in the HF and low (67%) in the LF soil, as were microbial biomass C and P concentrations. The ¹⁴C that remained in the microbial biomass at the end of the 6-month incubation was higher in the LF soil (15%) than in the HF soil (11%). Fluctuations in P_i in the LF soil during incubation were small compared with those in HF soil, suggesting that P was cycling through microbial biomass. The concentrations of P_i were significantly greater in the HF samples throughout the incubation than in the LF samples. Net N mineralization and nitrification rates were also low in the LF soils, indicating a slow turnover of microorganisms under limited nutrient supply. Addition of N had little effect on biomass ¹⁴C and glucose utilization. This suggests that, at limiting P fertility, C turnover is retarded because microbial biomass becomes less efficient in the utilization of substrates. Received: 18 October 1999     

Dynamics of microbial biomass and nitrogen supply during primary succession on blastfurnace slag dumps in dry tropics

This paper reports the role of microbial biomass in the establishment of N pools in the substratum during primary succession (till 40-year age) in Blastfurnace Slag Dumps, an anthropogenically created land form in the tropics. Initially in the depressions in the slag dumps fine soil particles (silt+clay) accumulate, retaining moisture therein, and providing microsites for the accumulation of microbial biomass. In all sites microbial biomass showed distinct seasonality, with summer-peak and rainy season-low standing crops. During the summer season microbial biomass C ranged from 18.6 μg g⁻¹ in the 1-year old site to ca. 235 μg g⁻¹ in the 40-year old site; correspondingly, microbial biomass N ranged from 1.22 to 40 μg g⁻¹. On sites 2.5-years of age and younger, the microbial biomass N content accounted for more than 50% of the organic N in the soil, whereas the proportion of microbial biomass N was ca. 7% of organic N in 40-year old site. The strong correlation between microbial biomass and total N in soil indicated a significant role of microbes in the build-up of nitrogen during the initial stages of succession in the slag dumps. Though the organic N pool in the soil was low (594 mg kg⁻¹) even after 40 years of succession, the available N (NH₄-N and NO₃-N) contents in the soil were generally high through the entire age series (ca. 16-32 μg g⁻¹) during the rainy season (which supports active growth of the herbaceous community). The high mineral-N status on the slag dump was related with high N-mineralization rates, particularly in the young sites (20.6 and 13.9 μg g⁻¹ month⁻¹ at 1 and 2.5-year age). We suggest that along with the abiotic factors having strong effect on ecosystem functioning, the microbial biomass, an important biotic factor, shows considerable influence on soil nutrient build-up during early stages of primary succession on the slag dumps. The microbial biomass dynamics initiates biotic control in developing slag dumps ecosystem through its effect on nitrogen pools and availability.     

Effects of Cd,Zn, or both on soil microbial biomass and activity in a clay loam soil

We investigated Cd, Zn, and Cd + Zn toxicity to soil microbial biomass and activity, and indigenous Rhizobium leguminosarum biovar trifolii, in two near neutral pH clay loam soils, under long-term arable and grassland management, in a 6-month laboratory incubation, with a view to determining the causative metal. Both soils were amended with Cd- or Zn-enriched sewage sludge, to produce soils with total Cd concentrations at four times (12 mg Cd g⁻¹ soil), and total Zn concentrations (300 mg Zn kg⁻¹ soil) at the EU upper permitted limit. The additive effects of Cd plus Zn at these soil concentrations were also investigated. There were no significant differences in microbial biomass C (B _C), biomass ninhydrin N (B _N), ATP, or microbial respiration between the different treatments. Microbial metabolic quotient (defined as qCO₂ = units of CO₂–C evolved unit⁻¹ biomass C unit⁻¹ time) also did not differ significantly between treatments. However, the microbial maintenance energy (in this study defined as qCO₂-to-μ ratio value, where μ is the growth rate) indicated that more energy was required for microbial synthesis in metal-rich sludge-treated soils (especially Zn) than in control sludge-treated soils. Indigenous R. leguminosarum bv. trifolii numbers were not significantly different between untreated and sludge-treated grassland soils after 24 weeks regardless of metal or metal concentrations. However, rhizobial numbers in the arable soils treated with metal-contaminated sludges decreased significantly (P < 0.05) compared to the untreated control and uncontaminated sludge-treated soils after 24 weeks. The order of decreasing toxicity to rhizobia in the arable soils was Zn > Cd > Cd + Zn.     

The role of tree leaf mulch and nitrogen fertilizer on turfgrass soil quality

 The influence of tree leaf amendment and N fertilization on soil quality in turfgrass environments was evaluated. Our objective was to assess changes in soil quality after additions of leaf materials and N fertilization by monitoring soil chemical and physical parameters, microbial biomass and soil enzymes. Established perennial ryegrass (Lolium perenne) plots were amended annually with maple (Acer spp.) leaves at three different rates (0, 2240, and 4480 kg ha^–1 year^–1) and treated with three nitrogen rates (0, 63, and 126 kg N ha^–1 year^–1). Tree leaf mulching did not significantly affect water infiltration or bulk density. However, trends in the data suggest increased infiltration with increasing leaf application rate. Tree leaf mulching increased total soil C and N at 0–1.3 cm depth but not at 1.3–9.0 cm. Extracted microbial phospholipid, an indicator of microbial biomass size, ranged from 28 to 68 nmol phospholipid g^–1 soil at the 1.3–9.0 cm depth. The activity of β-glucosidase estimated on samples from 0–1.3 cm and 1.3–9.0 cm depths, and dehydrogenase activity estimated on samples from 1.3–9.0 cm were significantly increased by leaf mulching and N fertilizer application. Changes in microbial community composition, as indicated by phospholipid fatty acid methyl ester analysis, appear to be due to seasonal variations and did not reflect changes due to N or leaf amendment treatments. There were no negative effects of tree leaf mulching into turfgrass and early data suggest this practice will improve soil chemical, physical, and biological structure. Received: 10 December 1997     

Carbon and nitrogen relationships in the microbial biomass of soils in beech (Fagus sylvatica L.) forests

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.     

Microbial use of organic amendments in saline soils monitored by changes in the C/C ratio

An incubation experiment was carried out to investigate whether salinity at high pH has negative effects on microbial substrate use, i.e. the mineralization of the amendment to CO₂ and inorganic N and the incorporation of amendment C into microbial biomass C. In order to exploit natural differences in the ¹³C/¹²C ratio, substrate from two C₄ plants, i.e. highly decomposed and N-rich sugarcane filter cake and less decomposed N-poor maize leaf straw, were added to two alkaline Pakistani soils differing in salinity, which had previously been cultivated with C₃ plants. In soil 1, the additional CO₂ evolution was equivalent to 65% of the added amount in the maize straw treatment and to 35% in the filter cake treatment. In the more saline soil 2, the respective figures were 56% and 32%. The maize straw amendment led to an identical immobilization of approximately 48 μg N g⁻¹ soil over the 56-day incubation in both soils compared with the control soils. In the filter cake treatment, the amount of inorganic N immobilized was 8.5 μg N g⁻¹ higher in soil 1 than in soil 2 compared with the control soils. In the control treatment, the content of microbial biomass C₃-C in soil 1 was twice that in soil 2 throughout the incubation. This fraction declined by about 30% during the incubation in both soils. The two amendments replaced initially similar absolute amounts of the autochthonous microbial biomass C, i.e. 50% of the original microbial biomass C in soil 1 and almost 90% in soil 2. The highest contents of microbial biomass C₄-C were equivalent to 7% (filter cake) and 11% (maize straw) of the added C. In soil 2, the corresponding values were 14% lower. Increasing salinity had no direct negative effects on microbial substrate use in the present two soils. Consequently, the differences in soil microbial biomass contents are most likely caused indirectly by salinity-induced reduction in plant growth rather than directly by negative effects of salinity on soil microorganisms.     

Adenylates in the soil microbial biomass at different temperatures

Five soils from temperate sites (Germany; 2 arable and 3 grassland) were incubated aerobically at 5, 10, 15, 20, 25, 35, and 40 °C for 8 days. Soils were analysed for soil microbial biomass C, biomass N, AMP, ADP, and ATP to determine whether the increase in the ATP-to-microbial biomass C ratio with increasing temperature was either due to an increase in the adenylate energy charge (AEC) or de novo synthesis of ATP, or both. Around 80% of the variance in microbial biomass C and biomass N was explained by differences in soil properties, only 7% by the temperature treatments. Averaging the data of all 5 soils for each incubation temperature, the microbial biomass C content decreased with increasing temperature from 15 to 40 °C continuously by 2.5 μg g⁻¹ soil °C⁻¹ after 8-days' incubation. However, this decrease was not accompanied by a similar decrease in microbial biomass N. The average microbial biomass C/N ratio was 6.8. Between 54 and 76% of the variance in AMP, ADP, ATP and the sum of adenylates was explained by differences in soil properties and between 14 (ADP) and 27% (ATP) by the temperature treatments. However, temperature effects on AMP and ADP were variable and inconsistent. In contrast, ATP and consequently also the sum of adenylates increased continuously from 5 to 30 °C followed by a decline to 40 °C. The AEC showed similarly a small, but significant increase with increasing temperature from 0.73 to 0.85 at 30 °C. Consequently, the majority of the variance, i.e. roughly 60% in AEC values, but also in ATP-to-microbial biomass C ratios was explained by the incubation temperature. The mean ATP-to-microbial biomass C ratio increased from 4.7 μmol g⁻¹ at 5 °C to a 2.5 fold maximum of 12.0 μmol g⁻¹ at 35 °C. This increase was linear with a rate of 0.26 μmol ATP g⁻¹ microbial biomass C °C⁻¹. The energy for the extra ATP produced during temperature increase is probably derived from an accelerated turnover of endocellular C reserves in the microbial biomass.     

Nitrogen dynamics and microbial response in soil amended with either olive pulp or its by-products after biogas production

Olive pulp (OP), the residual material of a two-phase olive oil extraction system, and effluents from hydrogen (EH₂) and methane (ECH₄) production, have been evaluated as soil amendments particularly for their impact on soil mineral nitrogen (N) dynamics, gross N mineralization, and soil microbial biomass N (N_mic). Both N transformation and microbial growth were mainly influenced by the amount and quality of added organic carbon (C). Both OP and EH₂, which contain more carbohydrates and lipids than polyphenolic compounds, stimulated NO₃ ⁻ immobilization during the early incubation period and increased N_mic, saprophytic fungi, and N mineralization. On the contrary, soil amended with ECH₄, which is characterized by the lowest C content but the highest content of polyphenolic compounds, behaved as the control; neither NO₃ ⁻ immobilization nor microbial growth were observed and gross N mineralization was stimulated only at the beginning of the incubation period. Bacterial plate count was significantly correlated with direct bacterial count and fungal count was correlated with N_mic. Therefore, it is suggested that both bacterial and fungal plate counts may be used as indicators of the overall bacterial and fungal populations inhabiting soil, respectively. The knowledge of the impact of these materials on soil N dynamics is crucial for their correct use in agriculture because it has been shown that NO₃ ⁻ availability can be strongly influenced by the addition of different amounts and quality of organic amendment.     

Interactions of mustard plants and soil microorganisms after application of sugarcane filter cake and pea residues to an Andosol

In a pot experiment using a strongly P‐fixing Andosol from Nicaragua, the effects of sugarcane–filter cake application on the growth of white mustard (Sinapis alba L.) were compared with those of ¹³C‐labeled pea residues. The application of pea residues led to a 50% increase and the application of filter cake to a 30% decrease in soil organic matter–derived microbial biomass C compared with the control. In contrast, the application of filter cake resulted in a four times higher content of substrate‐derived microbial biomass C than that of pea residues. The application of organic substrates generally increased microbial biomass N. Mustard growth led to significant increases in microbial biomass P in the control, but also in the organic‐amendment treatments, which always resulted in decreased microbial biomass C : P ratios. Mustard growth also led to increased contents of Bray‐1‐extractable P, but this increase was only significant in the filter cake treatment. The application of pea residues had no effect on the yield of shoot C, but a positive effect on the yield of root C in comparison with the nonamended control. In contrast, the application of filter cake significantly depressed yields of shoot C and root C, due to N immobilization, presumably due to the high concentration of lignin.     

Soil microbial biomass activation by trace amounts of readily available substrate

The soil microbial biomass survives as a largely dormant population for long periods without fresh substrates, depending for growth upon a rapid uptake of substrates when they become available. Currently, little investigation has been made into the mechanisms involved in the transition from dormancy to activity. We found that additions of trace amounts of different simple and complex substrates (glutamic acid, amino acids mixture, glucose, protein hydrolysates, carbohydrates, compost extract), even at very low application rates (5-μg C g⁻¹ soil), caused an immediate and significant activation (measured as increased CO₂-C evolved) of the soil microbial biomass. The different substrates caused different intensities of respiration response, which were related to the substrates’ composition, complexity, and degradability. The difference between the CO₂-C evolved from the amended soil minus that evolved from a similarly incubated but non-amended soil ranged from 80 to 160% of the humified carbon C added as substrate, with most of the substrates causing a positive priming effect, in agreement with previous findings. The activation ended after 5–70 h, depending on the substrate, but the microbial biomass could be reactivated with further additions. It seems that the microbial biomass first responds to traces of substrate by increasing its metabolic activity in anticipation of a larger ‘food event’. Overall, these results indicate that soil micro-organisms have evolved metabolic and physiological strategies that allow them to survive and growth in the generally poor-substrate soil environment.Contribution presented at the Exploratory Workshop: ‘Non-molecular manipulation of soil microbial communities’, held at the University of Udine, Udine, Italy from 17 to 20 October, 2004. The workshop was funded by the European Science Foundation and the University of Udine.     

Salinity and sodicity effects on respiration and microbial biomass of soil

An understanding of the effects of salinity and sodicity on soil carbon (C) stocks and fluxes is critical in environmental management, as the areal extents of salinity and sodicity are predicted to increase. The effects of salinity and sodicity on the soil microbial biomass (SMB) and soil respiration were assessed over 12weeks under controlled conditions by subjecting disturbed soil samples from a vegetated soil profile to leaching with one of six salt solutions; a combination of low-salinity (0.5dSm⁻¹), mid-salinity (10dSm⁻¹), or high-salinity (30dSm⁻¹), with either low-sodicity (sodium adsorption ratio, SAR, 1), or high-sodicity (SAR 30) to give six treatments: control (low-salinity low-sodicity); low-salinity high-sodicity; mid-salinity low-sodicity; mid-salinity high-sodicity; high-salinity low-sodicity; and high-salinity high-sodicity. Soil respiration rate was highest (56–80mg CO₂-C kg⁻¹ soil) in the low-salinity treatments and lowest (1–5mg CO₂-C kg⁻¹ soil) in the mid-salinity treatments, while the SMB was highest in the high-salinity treatments (459–565mg kg⁻¹ soil) and lowest in the low-salinity treatments (158–172mg kg⁻¹ soil). This was attributed to increased substrate availability with high salt concentrations through either increased dispersion of soil aggregates or dissolution or hydrolysis of soil organic matter, which may offset some of the stresses placed on the microbial population from high salt concentrations. The apparent disparity in trends in respiration and the SMB may be due to an induced shift in the microbial population, from one dominated by more active microorganisms to one dominated by less active microorganisms.