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     

Spatial changes of soil fungal and bacterial biomass from a sub-alpine coniferous forest to grassland in a humid, sub-tropical region

 Fungal and bacterial biomass were determined across a gradient from a forest to grassland in a sub-alpine region in central Taiwan. The respiration-inhibition and ergosterol methods for the evaluation of the microbial biomass were compared. Soil fungal and bacterial biomass both significantly decreased (P<0.05) with the shift of vegetation from forest to grassland. Fungal and bacterial respiration rates (evolved CO₂) were, respectively, 89.1 μl CO₂ g^–1 soil h^–1 and 55.1 μl CO₂ g^–1 soil h^–1 in the forest and 36.7 μl CO₂ g^–1 soil h^–1 and 35.7 μl CO₂ g^–1 soil h^–1 in the grassland surface soils (0–10 cm). The fungal ergosterol content in the surface soil decreased from the forest zone (108 μg g^–1) to the grassland zone (15.9 μg g^–1). A good correlation (R ²=0.90) was exhibited between the soil fungal ergosterol content and soil fungal CO₂ production (respiration) for all sampling sites. For the forest and grassland soil profiles, microbial biomass (respiration and ergosterol) declined dramatically with depth, ten- to 100-fold from the surface organic horizon to the deepest mineral horizon. With respect to fungal to bacterial ratios for the surface soil (0–10 cm), the forest zone had a significantly (P<0.05) higher ratio (1.65) than the grassland zone (1.05). However, there was no fungal to bacterial ratio trend from the surface horizon to the deeper mineral horizons of the soil profiles. Received: 30 March 2000     

Carbon dioxide emissions and net primary production of Russian terrestrial ecosystems

 Determination of the C balance is of considerable importance when forecasting climate and environmental changes. Soil respiration and biological productivity of ecosystems (net primary production; NPP) are the basic components of the terrestrial C cycle. In this study, a previously made assessment of the annual CO₂ flux from Russian soils was improved upon. CO₂ emissions from Russian soils during the growing period were shown to represent, on average, 53–82% of the annual CO₂ flux from Russian soils. The total annual CO₂ flux from Russian soils was estimated at 4.50 Gt C (C source). The NPP of Russian ecosystems was estimated at 4.81 Gt C year^–1 (C sink). Our calculations showed values of CO₂ emissions and the C sink to be very close. This shows that, in general, terrestrial ecosystems are under steady state. Received: 1 December 1997     

Grazing intensity alters soil respiration in an alpine meadow on the Tibetan plateau

Grazing intensity may alter the soil respiration rate in grassland ecosystems. The objectives of our study were to (1) determine the influence of grazing intensity on temporal variations in soil respiration of an alpine meadow on the northeastern Tibetan Plateau; and (2) characterise the temperature response of soil respiration under different grazing intensities. Diurnal and seasonal soil respiration rates were measured for two alpine meadow sites with different grazing intensities. The light grazing (LG) meadow site had a grazing intensity of 2.55 sheep ha⁻¹, while the grazing intensity of the heavy grazing (HG) meadow site, 5.35 sheep ha⁻¹, was approximately twice that of the LG site. Soil respiration measurements showed that CO₂ efflux was almost twice as great at the LG site as at the HG site during the growing season, but the diurnal and seasonal patterns of soil respiration rate were similar for the two sites. Both exhibited the highest annual soil respiration rate in mid-August and the lowest in January. Soil respiration rate was highly dependent on soil temperature. The Q₁₀ value for annual soil respiration was lower for the HG site (2.75) than for the LG site (3.22). Estimates of net ecosystem CO₂ exchange from monthly measurements of biomass and soil respiration revealed that during the period from May 1998 to April 1999, the LG site released 2040 g CO₂ m⁻² y⁻¹ to the atmosphere, which was about one third more than the 1530 g CO₂ m⁻² y⁻¹ released at the HG site. The results suggest that (1) grazing intensity alters not only soil respiration rate, but also the temperature dependence of soil CO₂ efflux; and (2) soil temperature is the major environmental factor controlling the temporal variation of soil respiration rate in the alpine meadow ecosystem.     

Nitrogen dynamics in different types of pasture in the Austrian Alps

 Soil N dynamics were compared in Alpine pastures on two mountains. N-pool sizes and N fluxes were measured relative to N losses via leaching and denitrification in summer. On each mountain, four types of pasture were studied: (1) forest pastures, (2) recently developed pastures formed by forest clearance ("new pastures"), (3) older established pastures, and (4) pastures planted with clover. At both study sites (Scheuchegg and Teufelstein) we obtained similar results. Compared with forest pasture soils, open pasture soils were found to have greater microbial biomass and faster mineralisation potentials, but net field mineralisation rates were slower. In the forest pastures, highest N losses via denitrification were found. Higher potential leaching of NO₃ ^–, estimated by accumulation of NO₃ ^– on ion-exchange resins, in the forest pasture soils suggests lower N uptake by microbes and herbaceous plants compared with open pastures. N₂O-production rates of the forest pasture soils at the Scheuchegg site (11.54 μg N₂O-N m^–2 h^–1) were of similar magnitude to those reported for spruce forests without pastures, but at Teufelstein (53.75 μg N₂O-N m^–2 h^–1) they were higher. However, if forest pastures are not overgrazed, no elevated N loss through N₂O production and leaching of NO₃ ^– is expected. Denitrification rates in the open pastures (0.83–7.50 μg N₂O-N m^–2 h^–1) were low compared with reports on lowland pastures. In soils of the new pastures, rates of microbial N processes were similar to those in the established pastures, indicating a high capacity of soils to restore their internal N cycle after forest clearance. Received: 19 August 1999     

Nitrous oxide emission from Swedish forest soils in relation to liming and simulated increased N-deposition

Fluxes of N₂O were studied in a Norway spruce forest in the southwest of Sweden. Three differently treated catchments were compared: Limed (6 t dolomite ha^–1), Nitrex (additional N-deposition corresponding to 35 kg ha^–1 year^–1, in small doses) and Control (used as control site). The N-retention was still high (95%) after 2years of N-addition at the Nitrex site when the flux measurements were performed. Each catchment contained both well-drained and poorly drained soils (covered with Sphagnum sp.). The emissions of N₂O were in general low with both a high spatial and temporal variation for all three sites. The measured emissions were 25, 71 and 96 (gN₂O-N ha^–1 year^–1) for the well-drained Limed, Control and Nitrex sites, respectively. The average emissions of N₂O from the wet areas were significantly higher than the well-drained areas within the catchments. For the wet areas the measured emissions were larger: 90, 118 and 254 (g N₂O-N ha^–1 year^–1) for the Limed, Control and Nitrex sites, respectively. Comparison between treatments showed the wet Nitrex site to have a significantly higher emission than all other sites. The increased N-deposition at the Nitrex site increased the N₂O emissions by 0.2% of the added N for the well-drained soils and about 1% for the wet areas, compared with the control site. Since the wet areas represented only a small part of the forest, their larger emissions did not contribute significantly to the overall emission of the forest. Neither temperature nor water content of the soil was well correlated with the N₂O emissions. Soil gas samples showed that most of the N₂O was produced below a 0.3-m depth in the soil. Received: 27 September 1996     

Soil respiration, nitrogen mineralization and uptake in barley following cultivation of grazed grasslands

 Soil tillage was studied as a strategy to synchronize N mineralization with plant demand following ploughing of two types of grazed pastures [ryegrass/white clover (Lolium perenne/Trifolium repens) and pure ryegrass]. The swards were either rotovated and ploughed or ploughed only. Soil respiration, as determined by a dynamic chamber method, was related to net N mineralization and to plant N uptake in a subsequent spring barley crop (Hordeum vulgare). Diurnal variations in temperature were important for the CO₂ flux and care must be taken that temperatures during measuring periods are representative of the daily mean. Soil tillage increased the CO₂ flux considerably compared with untilled soil with total emissions of 2.6 and 1.4 t C ha^–1, respectively, from start of April to end of June. Sward type or rotovation did not markedly influence accumulated emissions. Rotovation significantly increased the content of nitrate in the soil until 43 days after rotovation, showing that net N mineralization occurred rapidly during this period, in spite of low soil temperatures (5–10  °C). Rotovation increased barley grain yield by 10–12% and N-uptake by 14%. For both sward types, rotovation caused an extra N-uptake in harvested plant material of about 12 kg ha^–1. The availability of soil inorganic N at the early stages of barley was important for the final yield and N-uptake. The results indicated that soil biological activity was not enhanced by rotovation and that the yield effect of rotovation was mainly caused by quicker availability and better synchrony between N mineralization and plant uptake due to earlier start of decomposition. Received: 3 May 2000     

Measuring forest floor CO2 fluxes in a Douglas-fir forest

CO₂ exchange was measured on the forest floor of a coastal temperate Douglas-fir forest located near Campbell River, British Columbia, Canada. Continuous measurements were obtained at six locations using an automated chamber system between April and December, 2000. Fluxes were measured every half hour by circulating chamber headspace air through a sampling manifold assembly and a closed-path infrared gas analyzer. Maximum CO₂ fluxes measured varied by a factor of almost 3 between the chamber locations, while the highest daily average fluxes observed at two chamber locations occasionally reached values near 15 μmol C m⁻² s⁻¹. Generally, fluxes ranged between 2 and 10 μmol C m⁻² s⁻¹ during the measurement period. CO₂ flux from the forest floor was strongly related to soil temperature with the highest correlation found with 5 cm depth temperature. A simple temperature dependent exponential model fit to the nighttime fluxes revealed Q₁₀ values in the normal range of 2–3 during the warmer parts of the year, but values of 4–5 during cooler periods. Moss photosynthesis was negligible in four of the six chambers, while at the other locations, it reduced daytime half-hourly net CO₂ flux by about 25%. Soil moisture had very little effect on forest floor CO₂ flux. Hysteresis in the annual relationship between chamber fluxes and soil temperatures was observed. Net exchange from the six chambers was estimated to be 1920±530 g C m⁻² per year, the higher estimates exceeding measurement of ecosystem respiration using year-round eddy correlation above the canopy at this site. This discrepancy is attributed to the inadequate number of chambers to obtain a reliable estimate of the spatial average soil CO₂ flux at the site and uncertainty in the eddy covariance respiration measurements.     

Spatial variability in the carbon of microbial biomass and microbial respiration in soils of the south of Moscow oblast

Soil samples from the upper 10-cm-thick layer of the humus horizon (without forest litter) were taken in Podol’sk and Serpukhov districts (1130 and 1080 km², respectively) of Moscow oblast. At each sampling site, ecosystem (forest, plowland, or fallow), soil (soddy-podzolic, soddy-gley, bog-podzolic, meadow alluvial, gray forest, and anthropogenically transformed soils of lawns and industrial zones), predominant vegetation, and topography (floodplain and low, medium, and upper parts of watersheds) were determined. The carbon content of the microbial biomass (C_mic) was determined by the method of substrate-induced respiration; we also determined the rate of basal (microbial) respiration (BR) and the organic carbon content, pH, and particle-size distribution. Overall, 237 samples from Serpukhov district and 45 samples from Podol’sk district were analyzed. The BR/C_mic ratios (respiration quotient qCO₂) and C_mic/C_org ratios were calculated. The C_mic content in the soils ranged from 43 to 1394 μg C/kg; the BR varied from 0.06 to 25 μg CO₂-C/g per h, qCO₂, from 0.34 to 6.52 μg CO₂-C/mg C_mic per h; and the C_mic/C_org ratio, from 0.19 to 10.65%. It was found that the most significant factors affecting the variability of the C_mic and BR are the parameters of ecosystem (50% and 80%, respectively) and soil (30% and 9%, respectively). The most significant variability of these indices was found in forest soils; it was mainly controlled by the soil texture (33 and 23%) and the C_org content (19 and 24%). The C_mic parameter made it possible to differentiate the soils of the territory for the purposes of their evaluation, monitoring, and biological assessment more clearly than the BR value and the soil chemical characteristics.     

Carbon dioxide emissions from agrogray soils under climate changes

The effect of droughts and drying-wetting cycles on the respiration activity of agrogray soils was studied in field and laboratory experiments. The alternation of drought periods and rains during the vegetation season did not increase the annual emission of CO₂ from the soils under a sown meadow and an agrocenosis. In laboratory experiments, the wetting of dried soil released 1–1.5% of C_org with a high decomposition constant n × 10⁻¹ day⁻¹ and a very short renewal time (2.1–2.4 days); therefore, an abrupt change in the wetting conditions did not intensify the loss of soil carbon under field conditions.     

Winter soil CO2 efflux and its contribution to annual soil respiration in different ecosystems of a forest-steppe ecotone, north China

Most soil respiration measurements are conducted during the growing season. In tundra and boreal forest ecosystems, cumulative winter soil CO₂ fluxes are reported to be a significant component of their annual carbon budgets. However, little information on winter soil CO₂ efflux is known from mid-latitude ecosystems. Therefore, comparing measurements of soil respiration taken annually versus during the growing season will improve the accuracy of ecosystem carbon budgets and the response of soil CO₂ efflux to climate changes. In this study we measured winter soil CO₂ efflux and its contribution to annual soil respiration for seven ecosystems (three forests: Pinus sylvestris var. mongolica plantation, Larix principis-rupprechtii plantation and Betula platyphylla forest; two shrubs: Rosa bella and Malus baccata; and two meadow grasslands) in a forest-steppe ecotone, north China. Overall mean winter and growing season soil CO₂ effluxes were 0.15-0.26 μmol m⁻² s⁻¹ and 2.65-4.61 μmol m⁻² s⁻¹, respectively, with significant differences in the growing season among the different ecosystems. Annual Q₁₀ (increased soil respiration rate per 10 °C increase in temperature) was generally higher than the growing season Q₁₀. Soil water content accounted for 84% of the variations in growing season Q₁₀ and soil temperature range explained 88% of the variation in annual Q₁₀. Soil organic carbon density to 30 cm depth was a good surrogate for SR₁₀ (basal soil respiration at a reference temperature of 10 °C). Annual soil CO₂ efflux ranged from 394.76 g C m⁻² to 973.18 g C m⁻² using observed ecosystem-specific response equations between soil respiration and soil temperature. Estimates ranged from 424.90 g C m⁻² to 784.73 g C m⁻² by interpolating measured soil respiration between sampling dates for every day of the year and then computing the sum to obtain the annual value. The contributions of winter soil CO₂ efflux to annual soil respiration were 3.48-7.30% and 4.92-7.83% using interpolated and modeled methods, respectively. Our results indicate that in mid-latitude ecosystems, soil CO₂ efflux continues throughout the winter and winter soil respiration is an important component of annual CO₂ efflux.     

Topographic variation in heterotrophic and autotrophic soil respiration in a tropical seasonal forest in Thailand

Soil respiration is a carbon flux that is indispensable for determining carbon balance despite variations over time and space in forest ecosystems. In Kanchanaburi, western Thailand, we measured the soil respiration rates at different slope positions—ridge (plot R), upper slope (plot U), and lower slope (plot L)—on a hill in a seasonal tropical forest [mixed deciduous forest (MDF)] to determine the seasonal and spatial variations in soil respiration on the slope. The heterotrophic (organic layer and soil) and autotrophic (root) respiration was differentiated by trenching. Soil respiration rates showed clear seasonal patterns: high and low rates in rainy and dry seasons respectively, at all plots, and tended to decrease up the slope. Soil respiration rates responded significantly to soil water content in the 0–30?cm layer, but the response patterns differed between the lower slope (plot L) and the upper slope (plots R and U): a linear model could be applied to the lower slope but exponential quadratic models to the upper slope. The annual carbon dioxide (CO₂) efflux from the forest floor was also associated with the slope position and ranged from 1908?gC?m^?2?year^?1 in plot L to 1199?gC?m^?2?year^?1 in plot R. With ascending position from plot L to R, the contribution of autotrophic respiration increased from 19.4 to 36.6% of total soil respiration, while that of the organic layer decreased from 26.2 to 9.4%. Mineral soil contributed to 46.3 to 54.4% of the total soil respiration. Soil water content was the key factor in controlling the soil respiration rate and the contribution of the respiration sources. However, the variable responses of soil respiration to soil water content create a complex distribution of soil respiration at the watershed scale.     

Reduced net atmospheric CH4 consumption is a sustained response to elevated CO2 in a temperate forest

We compared, from 2004 through 2006, rates of soil–atmosphere CH₄ exchange at permanently established sampling sites in a temperate forest exposed to ambient (control plots; ∼380 μL L⁻¹) or elevated (ambient + 200 μL L⁻¹) CO₂ since August 1996. A total of 880 observations showed net atmospheric CH₄ consumption (flux from the atmosphere to the soil) from all static chambers most of the time at rates varying from 0.02 mg m⁻² day⁻¹ to 4.5 mg m⁻² day⁻¹. However, we infrequently found net CH₄ production (flux from the soil to the atmosphere) at lower rates, 0.01 mg m⁻² day⁻¹ to 0.08 mg m⁻² day⁻¹. For the entire study, the mean (±SEM) rate of net CH₄ consumption in control plots was higher than the mean for CO₂-enriched plots, 0.55 (0.03) versus 0.51 (0.03) mg m⁻² day⁻¹. Annual rates of 184, 196, and 197 mg m⁻² for net CH₄ consumption at control plots during the three calendar years of this study were 19, 10, and 8% higher than comparable values for CO₂ enriched plots. Differences between treatments were significant in 2004 and 2005 and nearly significant in 2006. Volumetric soil water content was consistently higher at CO₂-enriched sites and a mixed-effects model identified a significant soil moisture x CO₂ interaction on net atmospheric CH₄ consumption. Increased soil moisture at CO₂-enriched sites likely increases diffusional resistance of surface soils and the frequency of anaerobic microsites supporting methanogenesis, resulting in reduced rates of net atmospheric CH₄ consumption. Our study extends our observations of reduced net atmospheric CH₄ consumption at CO₂-enriched plots to nearly five continuous years, suggesting that this is likely a sustained negative feedback to increasing atmospheric CO₂ at this site.     

Effects of temperature,glucose and inorganic nitrogen inputs on carbon mineralization in a Tibetan alpine meadow soil

High levels of available nitrogen (N) and carbon (C) have the potential to increase soil N and C mineralization. We hypothesized that with an external labile C or N supply alpine meadow soil will have a significantly higher C mineralization potential, and that temperature sensitivity of C mineralization will increase. To test the hypotheses an incubation experiment was conducted with two doses of N or C supply at temperature of 5, 15 and 25 °C. Results showed external N supply had no significant effect on CO₂ emission. However, external C supply increased CO₂ emission. Temperature coefficient (Q₁₀) ranged from 1.13 to 1.29. Significantly higher values were measured with C than with N addition and control treatment. Temperature dependence of C mineralization was well-represented by exponential functions. Under the control, CO₂ efflux rate was 425 g CO₂–C m^?2 year^?1, comparable to the in situ measurement of 422 g CO₂–C m^?2 year^?1. We demonstrated if N is disregarded, microbial decomposition is primarily limited by lack of labile C. It is predicted that labile C supply would further increase CO₂ efflux from the alpine meadow soil.     

Evaluation of the selective respiratory inhibition method for measuring the ratio of fungal:bacterial activity in acid agricultural soils

A procedure for the measurement of the fungal and bacterial contribution to substrate-induced respiration was tested in three arable soils. Glucose and different amounts of cycloheximide (eukaryote inhibitor) and streptomycin sulfate (prokaryote inhibitor) were added to soil suspensions, and respiration (CO₂ evolution) was measured. Streptomycin sulfate concentrations from 10 to 120 mg ml^–1 soil solution caused a stable inhibition of respiration. Amounts of cycloheximide ranging from 5 to 35 mg ml^–1 showed an increasing inhibition. In a test with separate and combined addition of the antibiotics at maximum inhibitory concentrations, inhibition by streptomycin was completely overlapped by cycloheximide. This indicated non-target inhibition which may lead to overestimation of fungal respiration. Experiments with sterilized soils inoculated with either fungi or bacteria confirmed that streptomycin selectively inhibited bacteria. Cycloheximide, however, did not only inhibit fungal respiration already at 2 mg ml^–1, but also increasingly inhibited bacterial respiration at increasing concentrations. Only at less than 5 mg cycloheximide ml^–1 was the condition of selective fungal inhibition fulfilled. When 2 mg cycloheximide and 10 mg streptomycin sulfate ml^–1 were applied, the sum of the separate inhibitions almost equalled the combined inhibition by the mix of both inhibitors in field samples. This method yielded fungal:bacterial respiration ratios of 0.50 to 0.60, and confirmed the dominance of bacteria in Dutch arable soils. The ratios obtained by the selective inhibitors were not correlated with, and were higher than, ratios of fungal:bacterial biovolume (0.19 to 0.46) as determined by microscopy and image analysis. Similar measurements in a forest soil (A-horizon) raised doubts on the reliability of the fungal inhibition by cycloheximide in this soil. It is concluded that the separate:combined inhibition ratio should always be checked, and comparison with other approaches is recommended. Received: 17 September 1996     

Changing role of cultivated land in the global carbon cycle

 The carbon balance is ill defined for agricultural lands so that their role in global C balance cannot be accurately estimated. Changes in agriculture in the last 50 years have resulted in a general increase in grain yields, total net annual production (TNAP), and C input to the soil. Amounts of C returned annually with crop residues on Sanborn Field, one of the oldest experimental fields in the United States, increased after 1950, and this was accompanied by C accumulation in soils. Under wheat monocrop (with mineral fertilizer), C accumulated at a rate of 50 g m^–2 year^–1. A 3-year rotation (corn/wheat/clover) with manure and nitrogen applications sequestered 150 g m^–2 year^–1 of C. Total C balance for the wheat and corn production area in the United States, approximated on the basis of these rates, indicates that at least 32 Tg C was sequestered annually during the last 40–50 years. Received: 1 December 1997     

水稻土基底呼吸与CO2排放强度的日动态及长期不同施肥下的变化

土壤呼吸排放是陆地生态系统土气交换快速而活跃的途径之一,对大气CO2浓度的变化有显著的影响。本文对太湖地区一个代表性水稻土水稻收割后土壤基底呼吸CO2排放进行了昼夜观测和采样分析。结果表明,不同小区平均土壤呼吸与CO2排放速率在CO2-C.12.2～25.2.mg/(m2h)之间,日排放量在CO2-C.327.2～604.1mg/(m2d)之间,低于文献报道的森林和草地及旱作农田的土壤呼吸;与长期有机-无机配施处理相比,长期单施化肥CO2日排放量提高了55%～85%,并且显著提高了土壤呼吸对土壤(5.cm)温度的响应敏感性。相关分析表明,土壤呼吸CO2排放强度与土壤微生物N(Nmic)、微生物C∶N(Cmic/Nmic)和P的有效性有密切的关系;生物有效N和P的有效性显著地影响着土壤呼吸与CO2的生成和排放。本试验结果进一步支持了水稻土的固碳效应。但是,供试不同小区土壤呼吸排放强度的变异隐含着长期不同施肥处理可能使与高呼吸活性有关的微生物群落发生改变,有待于进一步研究。     

Comparison of two versions of the acetylene inhibition/soil core method for measuring denitrification loss from an irrigated wheat field

 Two versions of the acetylene inhibition (AI)/soil core method were compared for the measurement of denitrification loss from an irrigated wheat field receiving urea-N at a rate of 100 kg ha^–1. With AI/soil core method A, the denitrification rate was measured by analysing the headspace N₂O, followed by estimation of N₂O dissolved in the solution phase using Bunsen absorption coefficients. With AI/soil core method B, N₂O entrapped in the soil was measured in addition to that released from soil cores into the headspace of incubation vessels. In addition, the two methods were also compared for measurement of the soil respiration rate. Of the total N₂O produced, 6–77% (average 40%) remained entrapped in the soil, whereas for CO₂, the corresponding figures ranged from 12–65% (average 44%). The amount of the entrapped N₂O was significantly correlated with the water-filled pore space (WFPS) and with the N₂O concentration in the headspace, whereas CO₂ entrapment was dependent on the headspace CO₂ concentration but not on the WFPS. Due to the entrapment of N₂O and CO₂ in soil, the denitrification rate on several (18 of the 41) sampling dates, and soil respiration rate on almost all (27 of the 30) sampling dates were significantly higher with method B compared to method A. Averaged across sampling dates, the denitrification rate measured with method B (0.30 kg N ha^–1 day^–1) was twice the rate measured with method A, whereas the soil respiration rate measured with method B (34.9 kg C ha^–1 day^–1) was 1.6 times the rate measured with method A. Results of this study suggest that the N₂O and CO₂ entrapped in soil should also be measured to ensure the recovery of the gaseous products of denitrification by the soil core method. Received: 12 May 1998     

Determination of root and microbial contributions to the CO<Subscript>2</Subscript> emission from soil by the substrate-induced respiration method

The contributions of root and microbial respiration to the CO₂ emission from the surface of gray forest and soddy-podzolic soils under meadow and forest vegetation were determined in field and laboratory experiments. In the field, a new modification of the substrate-induced respiration (SIR) method was applied. According to this method, the contribution of root respiration was estimated at 41–50% for meadow cenoses and 33% for forest cenoses; similar values were obtained in the course of separate incubation of roots and soil in laboratory (42–57% and 29–32%, respectively) and with the use of the laboratory version of the SIR method (35–40% and 21–31%, respectively). The analysis of difference between the values of root respiration and microbial respiration obtained by the field and laboratory methods for the same experimental plots and the comparison of advantages and disadvantages of these methods made it possible to outline the ways for the further improvement of the field version of the SIR method.     

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.