Soil-released carbon dioxide from microbial biomass carbon in the cultivated soils of karst areas of southwest China

 Soil microbial biomass and the emission of CO₂ from the soil surface were measured in yellow soils (Ultisols) of the karst areas of southwest China. The soils are relatively weathered, leached and impoverished, and have a low input of plant residues. The measurements were made for a 1-year period and show a reciprocal relationship between microbial biomass and surface CO₂ efflux. The highest (42.6±2.8 mg CO₂-C m^–2 h^–1) and lowest (15.6±0.6 mg CO₂-C m^–2 h^–1) CO₂ effluxes are found in the summer and winter, respectively. The cumulative CO₂ efflux is 0.24 kg CO₂-C m^–2 year^–1. There is also a marked seasonal variation in the amount of soil microbial biomass carbon, but with the highest (644±71 μg C g^–1 soil) and lowest (270±24 μg C g^–1 soil) values occurring in the winter and summer, respectively. The cumulative loss of soil microbial biomass carbon in the top 10 cm of the soil was 608 μg C g^–1 year^–1 soil over 17 sampling times. The mean residence time of microbial biomass is estimated at 105 days, suggesting that the carbon in soil microbial biomass may act as a source of the CO₂ released from soils. Received: 13 July 1999     

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.     

Soil organic carbon stocks, storage profile and microbial biomass under different crop management systems in a tropical agricultural ecosystem

 We investigated the soil organic C and N stocks, storage profiles and microbial biomass as influenced by different crop management systems in a tropical agricultural ecosystem. The different crop management systems significantly affected the C and N stocks and microbial biomass C and N at different soil depths. Amongst the systems evaluated, the rice-wheat system maintained a higher soil organic C content. Inclusion of legumes in the system improved the soil organic matter level and also soil microbial biomass activity, vital for the nutrient turnover and long-term productivity of the soil. Irrespective of the cropping system, approximately 58.4%, 25.7% and 15.9% of the C was distributed in 0–15, 15–30 and 30–60 cm depths, respectively. Received: 10 October 1999     

Short-term effects of tillage systems on active soil microbial biomass

 Conservation tillage, and especially no-tillage, induce changes in the distribution of organic pools in the soil profile. In long-term field experiments, marked stratification of the total soil microbial biomass and its activity have been observed as consequence of the application of no-tillage to previously tilled soils. Our objective was to study the evolution of the total and active soil microbial biomass and mineralized C in vitro during the first crop after the introduction of no-tillage to an agricultural soil. The experiment was performed on a Typic Hapludoll from the Argentinean Pampa. Remaining plant residues, total and active microbial biomass and mineralized C were determined at 0–5 cm and 5–15 cm depths, at three sampling times: wheat tilling, silking and maturity. The introduction of no-tillage produced an accumulation of plant residues in the soil surface layer (0–5 cm), showing stratification with depth at all sampling dates. Active microbial biomass and C mineralization were higher under no-tillage than under conventional tillage in the top 5 cm of the profile. The total soil microbial biomass did not differ between treatments. The active soil biomass was highly and positive correlated with plant residues (r ²=0.617;P<0.01) and with mineralized C (r ²=0.732;P<0.01). Consequently, the active microbial biomass and mineralized C reflected immediately the changes in residue management, whereas the total microbial biomass seemed not to be an early indicator of the introduction of a new form of soil management in our experiment. Received: 23 February 1999     

Effects of increasing periods under intensive arable vegetable production on biological, chemical and physical indices of soil quality

 The effects on soil condition of increasing periods under intensive cultivation for vegetable production on a Typic Haplohumult were compared with those of pastoral management using soil biological, physical and chemical indices of soil quality. The majority of the soils studied had reasonably high pH, exchangeable cation and extractable P levels reflecting the high fertilizer rates applied to dairy pasture and more particularly vegetable-producing soils. Soil organic C (C_org) content under long-term pasture (>60 years) was in the range of 55 g C kg^–1 to 65 g C kg^–1. With increasing periods under vegetable production soil organic matter declined until a new equilibrium level was attained at about 15–20 g C kg^–1 after 60–80 years. The loss of soil organic matter resulted in a linear decline in microbial biomass C (C_mic) and basal respiratory rate. The microbial quotient (C_mic/C_org) decreased from 2.3% to 1.1% as soil organic matter content declined from 65 g C kg^–1 to 15 g C kg^–1 but the microbial metabolic quotient (basal respiration/C_mic ratio) remained unaffected. With decreasing soil organic matter content, the decline in arginine ammonification rate, fluorescein diacetate hydrolytic activity, earthworm numbers, soil aggregate stability and total clod porosity was curvilinear and little affected until soil organic C content fell below about 45 g C kg^–1. Soils with an organic C content above 45 g C kg^–1 had been under pasture for at least 30 years. At the same C_org content, soil biological activity and soil physical conditions were markedly improved when soils were under grass rather than vegetables. It was concluded that for soils under continuous vegetable production, practices that add organic residues to the soil should be promoted and that extending routine soil testing procedures to include key physical and biological properties will be an important future step in promoting sustainable management practices in the area. Received: 18 November 1997     

Carbon additions increase nitrogen availability in northern hardwood forest soils

 The effects of acetate additions to northern hardwood forest soils on microbial biomass carbon (C) and nitrogen (N) content, soil inorganic N levels, respirable C and potential net N mineralization and nitrification were evaluated. The experiment was relevant to a potential watershed-scale calcium (Ca) addition that aims to replace Ca depleted by long-term exposure to acid rain. One option for this addition is to use calcium-magnesium (Mg) acetate, a compound that is inexpensive and much more readily soluble than the Ca carbonate that is generally used for large-scale liming. Field plots were treated with sodium (NA) acetate, Na bicarbonate or water (control) and were sampled (forest floor – Oe and Oa combined) 2, 10 and 58 days following application. It was expected that the addition of C would lead to an increase in biomass C and N and a decrease in inorganic N. Instead, we observed no effect on biomass C, a decline in biomass N and an increase in N availability. One possible explanation for our surprising results is that the C addition stimulated microbial activity but not growth. A second, and more likely, explanation for our results is that the C addition did stimulate microbial growth and activity, but there was no increase in microbial biomass due to predation of the new biomass by soil fauna. The results confirm the emerging realization that the effects of increases in the flow of C to soils, either by deliberate addition or from changes in atmospheric CO₂, are more complex than would be expected from a simple C : N ratio analysis. Evaluations of large-scale manipulations of forest soils to ameliorate effects of atmospheric deposition or to dispose of wastes should consider microbial and faunal dynamics in considerable detail. Received: 13 March 1998     

Interactions between soil organic matter status, cropping history, method of quantification and sample pretreatment and their effects on measured aggregate stability

 The effects of sample pretreatment (field-moist, air-dried or tension rewetted) on aggregate stability measured by wet sieving or turbidimetry were compared for a group of soil samples ranging in organic C content from 20 to 40 g C kg^–1. Concentrations of total N, total and hot-water-extractable carbohydrate and microbial biomass C were linearly related to those of organic C. Aggregate stability measured by wet sieving using air-dried or field-moist samples and that measured by turbidimetry, regardless of sample pretreatment, increased curvilinearly with increasing soil organic C content. However, when tension-rewetted samples were used for wet sieving, aggregate stability was essentially unaffected by soil organic C content. Measurements of aggregate stability (apart from wet sieving using rewetted soils) were closely correlated with one another and with organic C, total and extractable carbohydrate and microbial biomass C content of the soils. The short-term effects of aggregate stability were also studied. Soils from under long-term arable management and those under long-term arable followed by 1 or 3 years under pasture had similar organic C contents, but aggregate stability measured by turbidimetry and by wet sieving using air-dried or field-moist samples increased with increasing years under pasture. Light fraction C, microbial biomass and hot-water-extractable carbohydrate concentrations also increased. It was concluded that both total and labile soil organic C content are important in relation to water-stable aggregation and that the use of tension-rewetted samples to measure stability by wet sieving is unsatisfactory since little separation of values is achieved. Received: 6 January 1999     

Ratios between estimates of microbial biomass content and microbial activity in soils

The content levels and activities of the microbiota were estimated in topsoils and in one soil profile at agricultural and forest sites of the Bornhöved Lake district in northern Germany. Discrepancies between data achieved by fumigation-extraction (FE) and substrate-induced respiration (SIR), both used for the quantification of microbial biomass, were attributed to the composition of the microbial populations in the soils. In the topsoils, the active, glucose-responsive (SIR) versus the total, chloroform-sensitive microbial (FE) biomass decreased in the order; field maize monoculture (field-MM)>field crop rotation (field-CR) and dry grassland>beech forest. This ratio decreased within the soil profile of the beech forest from the litter horizon down to the topsoil. Differences between microbial biomass and activities suggested varying biomass-specific transformation intensities in the soils. The metabolic quotient (qCO₂), defined as the respiration rate per unit of biomass, indicates the efficiency in acquiring organic C and the intensity of C mineralization, while biomass-specific arginine-ammonification (arginine-ammonification rate related to microbial biomass content) seems to be dependent on N availability. The qCO₂, calculated on the basis of the total microbial biomass, decreased for the topsoils in the same order as did the ratio between the active, glucose-responsive microbial biomass to the total, chloroform-sensitive microbial biomass, in contrast to qCO₂ values based on the glucose-responsive microbial biomass, which did not. There was no difference between the levels of biomass-specific arginine-ammonification in topsoils of the fertilized field-CR, fertilized field-MM, fertilized dry grassland and eutric alder forest, but levels were lower in the beech forest, dystric alder forest, and unfertilized wet grassland topsoils. Ratios between values of different microbiological features are suggested to be more useful than microbiological features related to soil weight when evaluating microbial populations and microbially mediated processes in soils.     

Influence of soil properties on microbial populations, activity and biomass in humid subtropical mountainous ecosystems of India

 Microbial populations, biomass, soil respiration and enzyme activities were determined in slightly acid organic soils of major mountainous humid subtropical terrestrial ecosystems, along a soil fertility gradient, in order to evaluate the influence of soil properties on microbial populations, activity and biomass and to understand the dynamics of the microbial biomass in degraded ecosystems and mature forest. Although the population of fungi was highest in the undisturbed forest (Sacred Grove), soil respiration was lowest in the 7-year-old regrowth and in natural grassland (approximately 373 μg g^–1 h^–1). Dehydrogenase and urease activities were high in "jhum" fallow, and among the forest stands they were highest in the 7-year-old regrowth. Microbial biomass C (MBC) depended mainly on the organic C status of the soil. The MBC values were generally higher in mature forest than in natural grassland, 1-year-old jhum fallow and the 4-year-old alder plantation. The MBC values obtained by the chloroform-fumigation-incubation technique (330–1656 μg g^–1) did not vary significantly from those obtained by the chloroform-fumigation-extraction technique (408–1684 μg g^–1), however, the values correlated positively (P<0.001). The enzyme activities, soil respiration, bacterial and fungal populations and microbial biomass was greatly influenced by several soil properties, particularly the levels of nutrients. The soil nutrient status, microbial populations, soil respiration and dehydrogenase activity were greater in Sacred Grove, while urease activity was greater in grassland. Received: 14 October 1998     

Effects of long-term waste water irrigation on soil organic matter, soil microbial biomass and its activities in central Mexico

 The effect of long-term waste water irrigation (up to 80 years) on soil organic matter, soil microbial biomass and its activities was studied in two agricultural soils (Vertisols and Leptosols) irrigated for 25, 65 and 80 years respectively at Irrigation District 03 in the Valley of Mezquital near Mexico City. In the Vertisols, where larger amounts of water have been applied than in the Leptosols, total organic C (TOC) contents increased 2.5-fold after 80 years of irrigation. In the Leptosols, however, the degradability of the organic matter tended to increase with irrigation time. It appears that soil organic matter accumulation was not due to pollutants nor did microbial biomass:TOC ratios and qCO₂ values indicate a pollutant effect. Increases in soil microbial biomass C and activities were presumably due to the larger application of organic matter. However, changes in soil microbial communities occurred, as denitrification capacities increased greatly and adenylate energy charge (AEC) ratios were reduced after long-term irrigation. These changes were supposed to be due to the addition of surfactants, especially alkylbenzene sulfonates (effect on denitrification capacity) and the addition of sodium and salts (effect on AEC) through waste water irrigation. Heavy metals contained in the sewage do not appear to be affecting soil processes yet, due to their low availability. Detrimental effects on soil microbial communities can be expected, however, from further increases in pollutant concentrations due to prolonged application of untreated waste water or an increase in mobility due to higher mineralization rates. Received: 28 April 1999     

Changes in 15N abundance and amounts of biologically active soil nitrogen

 Estimation of the capacity of soils to supply N for crop growth requires estimates of the complex interactions among organic and inorganic N components as a function of soil properties. Identification and measurement of active soil N forms could help to quantify estimates of N supply to crops. Isotopic dilution during incubation of soils with added ¹⁵NH₄ ⁺ compounds could identify active N components. Dilution of ¹⁵N in KCl extracts of mineral and total N, non-exchangeable NH4₄ ⁺, and N in K₂SO₄ extracts of fumigated and non-fumigated soil was measured during 7-week incubation. Samples from four soils varying in clay content from 60 to 710 g kg^–1 were used. A constant level of ¹⁵N enrichment within KCl and K₂SO₄ extracted components was found at the end of the incubation period. Total N, microbial biomass C and non-exchangeable NH₄ ⁺ contents of the soils were positively related to the clay contents. The mineralized N was positively related to the silt plus clay contents. The active soil N (ASN) contained 28–36% mineral N, 29–44% microbial biomass N, 0.3–5% non-exchangeable NH₄ ⁺ with approximately one third of the ASN unidentified. Assuming that absolute amounts of active N are related to N availability, increasing clay content was related to increased N reserve for crop production but a slower turnover. Received: 7 July 1998     

Effect of temperature on soil microbial biomass and its metabolic quotient in situ under different tillage systems

Variations in the microbial biomass and the in situ metabolic quotient (qCO₂) due to climatic conditions were determined in a typical soil from the Argentine Rolling Pampa. Microbial C was evaluated by fumigation-incubation and qCO₂ was calculated using soil respiration in the field. An inverse relationship between microbial C and soil temperature was fitted to a model (r ²=0.90, P=0.01). No significant association with the soil water content was detected because the soil was generally near field capacity and thus water availability did not limited microbial growth and activity. Values of qCO₂ increased (r ²=0.89, P=0.01) as the result of metabolic activatìon, likely induced by a higher maintenance energy requirement at high temperatures. The highest values of qCO₂ were obtained when microbial C was the lowest, which was attributed to self consumption of microbial C in the presence of high temperatures. Consequently, microbial C was generally higher (P=0.05) in winter than in summer. Therefore, when microbial C is used as an index of soil biological activity, the influence of temperature should be taken into account.     

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     

Urease activity and its relation to soil organic matter, microbial biomass nitrogen and urea-nitrogen assimilation by maize in a Brazilian Oxisol under no-tillage and tillage systems

 We studied the relationship between urease activity (UA) and soil organic matter (SOM), microbial biomass N (N_biom) content, and urea-N fertilizer assimilation by maize in a Dark Red Latosol (Typic Haplustox) cultivated for 9 years under no-tillage (NT), tillage with a disc plough (DP), and tillage with a moldboard plough (MP). Two soil depths were sampled (0–7.5 cm and 7.5–15 cm) at 4 different times during the crop cycle. Urea was applied at four different rates, ranging from 0 to 240 kg N ha^–1. The levels of fertilizer N did not affect the UA, SOM content, and N_biom content. No significant difference between the treatments (NT, DP, and MP) was observed for SOM during the experiment, probably because the major part of the SOM was in recalcitrant pools, since the area was previously cultivated (conventional tillage) for 20 years. The N_biom content explained 97% and 69% of the variation in UA in the upper and deeper soil layer, respectively. UA and biomass N were significantly higher in the NT system compared to the DP and MP systems. The highest maize productivity and urea-N recovery was also observed for the NT system. We observed that the increase in urea-N losses under NT, possibly as a consequence of a higher UA, was compensated for by the increase in N immobilized in the biomass. Received: 2 July 1999