外加碳酸盐增加石灰性土壤密闭培养过程中CO2的释放量

The closed-jar incubation method is widely used to estimate the mineralization of soil organic C. There are two C pools (i.e., organic and inorganic C) in calcareous soil. To evaluate the effect of additional carbonates on CO2 emission from calcareous soil during closed-jar incubation, three incubation experiments were conducted by adding different types (CaCO3 and MgCO3 ) and amounts of carbonate to the soil. The addition of carbonates significantly increased CO2 emission from the soil; the increase ranged from 12.0% in the CaCO3 amended soil to 460% in the MgCO3 amended soil during a 100-d incubation. Cumulative CO2 production at the end of the incubation was three times greater in the MgCO3 amended soil compared to the CaCO3 amended one. The CO2 emission increased with the amount of CaCO3 added to the soil. In contrast, CO2 emission decreased as the amount of MgCO3 added to the soil increased. Our results confirmed that the closed-jar incubation method could lead to an overestimate of organic C mineralization in calcareous soils. Because of its effect on soil pH and the dissolution of carbonates, HgCl2 should not be used to sterilize calcareous soil if the experiment includes the measurement of soil CO2 production.     

Soil CO2 evolution: Response from arginine additions

Short-term response of soil C mineralization following drying/rewetting has been proposed as an indicator of soil microbial activity. Houston Black clay was amended with four rates of arginine to vary microbial responses and keep other soil properties constant. The evolution of CO₂ during 1 and 3 days following rewetting of dried soil was highly related to CO₂ evolution during 10 days following chloroform fumigation (r² = 0.92 and 0.93, respectively) which is a widely used method for soil microbial biomass C, which disrupts cellular membranes. This study suggest that the release of CO₂ following rewetting of dried soil with no amendments other than heat and water can be highly indicative of soil microbial activity and possibly be used as a quantitative measurement of soil biological quality in Houston Black soils.     

Decomposition of maize straw in saline soil

The interactive effects of salinity and water on organic matter decomposition in soil are poorly known. A loamy topsoil adjusted to five concentrations of salinity (0, 31, 62, 93 and 124 mmol Na kg⁻¹ soil) using either NaCl or Na₂SO₄ was incubated at a water content of either 17 or 25% (w/w) in the dark at 28.5°C for 47 days, with maize straw added at 20 g kg⁻¹ soil. Comparing with non-saline soil, (1) NaCl salinity at all levels decreased cumulative CO₂ evolved during days 1–3 (averaged across two water levels), increased in the period 4–32 days at both water contents, and thereafter caused variable effects, depending upon water content and salinity; and (2) Na₂SO₄ salinity at various levels mainly caused no effect on cumulative CO₂ evolved during days 1–3 (averaged across two water levels), and thereafter (i.e. in days 4–47) caused mainly positive effects at 17% (w/w) water content and negative effects at 25% (w/w) water content. Cumulative CO₂ evolved over 47 days for both types of salinities was mainly greater at 17% (w/w) and smaller at 25% (w/w) water content compared with non-saline soil. Generally, at 25% (w/w) than at 17% (w/w) water content, there was a greater CO₂ evolved over 47 days, and also during different incubation phases for both types of salinities; the difference at low salinity levels was generally large and decreased as salinity increased. In conclusion, the salinity effect depends on soil water content and incubation period or decomposition phase.     

Turnover of soil organic matter and of microbial biomass under C3-C4 vegetation change: Consideration of C fractionation and preferential substrate utilization

Two processes contribute to changes of the δ¹³C signature in soil pools: ¹³C fractionation per se and preferential microbial utilization of various substrates with different δ¹³C signature. These two processes were disentangled by simultaneously tracking δ¹³C in three pools - soil organic matter (SOM), microbial biomass, dissolved organic carbon (DOC) - and in CO₂ efflux during incubation of 1) soil after C₃-C₄ vegetation change, and 2) the reference C₃ soil.The study was done on the Ap horizon of a loamy Gleyic Cambisol developed under C₃ vegetation. Miscanthus giganteus - a perennial C₄ plant - was grown for 12 years, and the δ¹³C signature was used to distinguish between ‘old’ SOM (>12 years) and ‘recent’ Miscanthus-derived C (<12 years). The differences in δ¹³C signature of the three C pools and of CO₂ in the reference C₃ soil were less than 1‰, and only δ¹³C of microbial biomass was significantly different compared to other pools. Nontheless, the neglecting of isotopic fractionation can cause up to 10% of errors in calculations. In contrast to the reference soil, the δ¹³C of all pools in the soil after C₃-C₄ vegetation change was significantly different. Old C contributed only 20% to the microbial biomass but 60% to CO₂. This indicates that most of the old C was decomposed by microorganisms catabolically, without being utilized for growth. Based on δ¹³C changes in DOC, CO₂ and microbial biomass during 54 days of incubation in Miscanthus and reference soils, we concluded that the main process contributing to changes of the δ¹³C signature in soil pools was preferential utilization of recent versus old C (causing an up to 9.1‰ shift in δ¹³C values) and not ¹³C fractionation per se.Based on the δ¹³C changes in SOM, we showed that the estimated turnover time of old SOM increased by two years per year in 9 years after the vegetation change. The relative increase in the turnover rate of recent microbial C was 3 times faster than that of old C indicating preferential utilization of available recent C versus the old C.Combining long-term field observations with soil incubation reveals that the turnover time of C in microbial biomass was 200 times faster than in total SOM. Our study clearly showed that estimating the residence time of easily degradable microbial compounds and biomarkers should be done at time scales reflecting microbial turnover times (days) and not those of bulk SOM turnover (years and decades). This is necessary because the absence of C reutilization is a prerequisite for correct estimation of SOM turnover. We conclude that comparing the δ¹³C signature of linked pools helps calculate the relative turnover of old and recent pools.     

Soil organic matter dynamics in grassland soils under elevated CO2: Insights from long-term incubations and stable isotopes

Elevated atmospheric carbon dioxide (CO₂) levels generally stimulate carbon (C) uptake by plants, but the fate of this additional C largely remains unknown. This uncertainty is due in part to the difficulty in detecting small changes in soil carbon pools. We conducted a series of long-term (170-330 days) laboratory incubation experiments to examine changes in soil organic matter pool sizes and turnover rates in soil collected from an open-top chamber (OTC) elevated CO₂ study in Colorado shortgrass steppe. We measured concentration and isotopic composition of respired CO₂ and applied a two-pool exponential decay model to estimate pool sizes and turnover rates of active and slow C pools. The active and slow C pools of surface soils (5-10 cm depth) were increased by elevated CO₂, but turnover rates of these pools were not consistently altered. These findings indicate a potential for C accumulation in near-surface soil C pools under elevated CO₂. Stable isotopes provided evidence that elevated CO₂ did not alter the decomposition rate of new C inputs. Temporal variations in measured δ¹³C of respired CO₂ during incubation probably resulted mainly from the decomposition of changing mixtures of fresh residue and older organic matter. Lignin decomposition may have contributed to declining δ¹³C values late in the experiments. Isotopic dynamics during decomposition should be taken into account when interpreting δ¹³C measurements of soil respiration. Our study provides new understanding of soil C dynamics under elevated CO₂ through the use of stable C isotope measurements during microbial organic matter mineralization.     

Electron donors and acceptors influence anaerobic soil organic matter mineralization in tidal marshes

Anaerobic decomposition in wetland soils is carried out by several interacting microbial processes that influence carbon storage and greenhouse gas emissions. To understand the role of wetlands in the global carbon cycle, it is critical to understand how differences in both electron donor (i.e., organic carbon) and terminal electron acceptor (TEA) availability influence anaerobic mineralization of soil organic matter. In this study we manipulated electron donors and acceptors to examine how these factors influence total rates of carbon mineralization and the pathways of microbial respiration (e.g., sulfate reduction versus methanogenesis). Using a field-based reciprocal transplant of soils from brackish and freshwater tidal marshes, in conjunction with laboratory amendments of TEAs, we examined how rates of organic carbon mineralization changed when soils with different carbon contents were exposed to different TEAs. Total mineralization (the sum of CO₂ + CH₄ produced) on a per gram soil basis was greater in the brackish marsh soils, which had higher soil organic matter content; however, on a per gram carbon basis, mineralization was greater in the freshwater soils, suggesting that the quality of carbon inputs from the freshwater plants was higher. Overall anaerobic metabolism was higher for both soil types incubated at the brackish site where SO₄²⁻ was the dominant TEA. When soils were amended with TEAs in the laboratory, more thermodynamically favorable respiration pathways typically resulted in greater organic matter mineralization (Fe(III) respiration > SO₄²⁻ reduction > methanogenesis). These results suggest that both electron donors and acceptors play important roles in regulating anaerobic microbial mineralization of soil organic matter.     

定期淹水强碱性盐渍土中14C标记葡萄糖和NH4+的动态

Flooding an extremely alkaline（pH 10.6） saline soil of the former Lake Texcoco to reduce salinity will affect the soil carbon（C）and nitrogen（N） dynamics.A laboratory incubation experiment was done to investigate how decreasing soil salt content affected dynamics of C and N in an extremely alkaline saline soil.Sieved soil with electrical conductivity（EC） of 59.2 dS m^-1 was packed in columns,and then flooded with tap water,drained freely and conditioned aerobically at 50%water holding capacity for a month.This process of flooding-drainage-conditioning was repeated eight times.The original soil and the soil that had undergone one,two,four and eight flooding-drainage-conditioning cycles were amended with 1000 mg glucose-¹⁴C kg^-1 soil and 200 mg NH₄⁺-N kg^-1soil,and then incubated for 28 d.The CO₂ emissions,soil microbial biomass,and soil ammonium（NE₄⁺）,nitrite（NO₂^-） and nitrate（NO₃^-） were monitored in the aerobic incubation of 28 d.The soil EC decreased from 59.2 to 1.0 dS m_¹ after eight floodings,and soil pH decreased from 10.6 to 9.6.Of the added ¹⁴C-labelled glucose,only 8%was mineralized in the original soil,while 24%in the soil flooded eight times during the 28-d incubation.The priming effect was on average 278 mg C kg^-1 soil after the 28-d incubation.Soil microbial biomass C(mean 66 mg C kg^-1 soil) did not change with flooding times in the unamended soil,and increased 1.4 times in the glucose-NH₄⁺-amended soil.Ammonium immobilization and NO₂^- concentration in the aerobically incubated soil decreased with increasing flooding times,while NO₃^- concentration increased.It was found that flooding the Texcoco soil decreased the EC sharply,increased mineralization of glucose,stimulated nitrification,and reduced immobilization of inorganic N,but did not affect soil microbial biomass C.     

Priming effects: Interactions between living and dead organic matter

In this re-evaluation of our 10-year old paper on priming effects, I have considered the latest studies and tried to identify the most important needs for future research. Recent publications have shown that the increase or decrease in soil organic matter mineralization (measured as changes of CO₂ efflux and N mineralization) actually results from interactions between living (microbial biomass) and dead organic matter. The priming effect (PE) is not an artifact of incubation studies, as sometimes supposed, but is a natural process sequence in the rhizosphere and detritusphere that is induced by pulses or continuous inputs of fresh organics. The intensity of turnover processes in such hotspots is at least one order of magnitude higher than in the bulk soil. Various prerequisites for high-quality, informative PE studies are outlined: calculating the budget of labeled and total C; investigating the dynamics of released CO₂ and its sources; linking C and N dynamics with microbial biomass changes and enzyme activities; evaluating apparent and real PEs; and assessing PE sources as related to soil organic matter stabilization mechanisms. Different approaches for identifying priming, based on the assessment of more than two C sources in CO₂ and microbial biomass, are proposed and methodological and statistical uncertainties in PE estimation and approaches to eliminating them are discussed. Future studies should evaluate directions and magnitude of PEs according to expected climate and land-use changes and the increased rhizodeposition under elevated CO₂ as well as clarifying the ecological significance of PEs in natural and agricultural ecosystems. The conclusion is that PEs - the interactions between living and dead organic matter - should be incorporated in models of C and N dynamics, and that microbial biomass should regarded not only as a C pool but also as an active driver of C and N turnover.     

Effects of copper on the decomposition of plant residues,microbial biomass,and β-glucosidase activity in soils

Abstract

Two types of soils (Brown Lowland soil and Ando soil), which were artificially enriched with different amounts of Cu, were incubated with or without pulverized orchard grass for 12 weeks at 25°C. For both soils with and without orchard grass amendment, the amount of CO₂ evolved over the 12-week period of incubation decreased by the enrichment with Cu at a concentration exceeding 1,000 mg kg^?1 soil. The decrease of the mineralization of added orchard grass in the Cu-enriched soil was conspicuous especially during the initial period of incubation. The amount of microbial biomass C at the end of the incubation was significantly reduced by the Cu enrichment regardless of the amendment with orchard grass. The relative decrease of the soil microbial biomass was much greater than that of the soil respiration. The amount of biomass C was negatively correlated with the amount of 0.1 M CaCl₂-extractable Cu as a logarithmic function. On the other hand, the β-glucosidase activity at the end of the incubation was not significantly affected by the presence of Cu in the soils without orchard grass amendment and increased with the increase in the amount of enriched Cu in the orchard grass-amended soils.     

A comparison of different indices for nitrogen mineralization

Indices of N mineralization in soils of contrasting texture, pH, and organic matter contents were compared at different dates during the growing season. The indices were derived from a 12-week aerobic incubation, determination of the amount of microbial biomass at the start of the incubation, determination of the increase in NH ₄ ⁺ after boiling with 2 M KCl for 2h, and extraction of total soluble N with 0.01 M CaCl₂. Cumulative mineral N increased linearly with time in the course of the incubations. Rates of mineralization in soil samples taken in March 1989 and 1990 were significantly correlated with soluble organic N, while correlations between the mineralization rate and the increase in NH ₄ ⁺ after boiling with 2 M KCl for 2 h were poor for sandy soils and absent for loamy soils. Correlations between NH ₄ ⁺ after boiling with 2 M KCl for 2h and the soil N concentration were highly significant, but no general relationship was found between the mineralization rate and the soil N concentration. Neither biomass N nor biomass C was significantly correlated with the mineralization rate or with one of the chemical indices. Among the methods tested, soluble organic N extracted with 0.01 M CaCl₂ was the only method with any promise for routine measurement of the mineralization capacity of the individual sites.     

Effect of Magnesium Chloride–Induced Salinity on Carbon Dioxide Evolution and Nitrogen Mineralization in a Silty Clay Loam Soil

A laboratory incubation experiment was conducted to evaluate the effect of magnesium chloride–induced salinity on carbon dioxide (CO₂) evolution and nitrogen (N) mineralization in a silty loam nonsaline alkaline soil. Magnesium chloride (MgCl₂) salinity was induced at 0, 4, 8, 12, 16, 20, 30, and 40.0 dS m^?1 and measured CO₂ evolution and N mineralization during 30 days of incubation. Both CO₂ evolution and N mineralization decreased significantly with increasing salinity. The cumulative CO₂ evolution decreased from 235 mg kg^?1 soil at electrical conductivity (EC) 0.65 dS m^?1 to 11.9 mg kg^?1 soil at 40 dS m^?1 during 30 days of incubation. Similarly, N mineralization decreased from 185.4 mg kg^?1 at EC 0.65 dS m^?1 to 34.45 mg kg^?1 at EC 40.0 dS m^?1 during the same period. These results suggested that increasing magnesium chloride salinity from 4 dS m^?1 adversely affect microbial activity in terms of carbon dioxide evolution and N mineralization.     

Estimating Soil Carbon,Nitrogen, and Phosphorus Mineralization from Short‐Term Carbon Dioxide Respiration

The measurement of soil carbon dioxide (CO₂) respiration is a means to gauge biological soil fertility. Test methods for respiration employed in the laboratory vary somewhat, and to date the equipment and labor required have limited more widespread adoption of such methodologies. A new method to measure soil respiration was tested along with the traditional alkali trap and titration method. The new method involves the Solvita gel system, which was originally designed for CO₂ respiration from compost but has been applied in this research to soils with treatments of increasing dairy manure compost. The objectives of this research are to (1) examine the relationship between the CO₂ release after 1 day of incubation from soils amended with dairy manure compost that have been dried and rewetted as determined using the titration method and the Solvita gel system, and (2) compare water‐soluble organic nitrogen (N), as well as carbon (C), N, and phosphorus (P) mineralization after 28 days of incubation with 1‐day CO₂ release from the titration method and Solvita gel system. One‐day CO₂ from both titration and the Solvita gel system were highly correlated with cumulative 28‐day CO₂ as well as the basal rate from 7–28 days of incubation. Both methods were also highly correlated with 28‐day N and P mineralization as well as the initial water‐extractable organic N and C concentration.

The data suggest that the Solvita gel system for soil CO₂ analysis could be a simple and easily used method to quantify soil microbial activity and possibly provide an estimate of potential mineralizable N and P. Once standardized soil sampling and laboratory analysis protocols are established, the Solvita method could be easily adapted to commercial soil testing laboratories as an index of soil microbial activity.     

Short‐term effects of polyacrylamide and dicyandiamide on C and N mineralization in a sandy loam soil

The soil conditioners anionic polyacrylamide (PAM) and dicyandiamide (DCD) are frequently applied to soils to reduce soil erosion and nitrogen loss, respectively. A 27‐day incubation study was set up to gauge their interactive effects on the microbial biomass, carbon (C) mineralization and nitrification activity of a sandy loam soil in the presence or absence of maize straw. PAM‐amended soils received 308 or 615 mg PAM/kg. Nitrogen (N)‐fertilized soils were amended with 1800 mg/kg ammonium sulphate [(NH₄)₂SO₄], with or without 70 mg DCD/kg. Maize straw was added to soil at the rate of 4500 mg/kg. Maize straw application increased soil microbial biomass and respiration. PAM stimulated nitrification and C mineralization, as evidenced by significant increases in extractable nitrate and evolved carbon dioxide (CO₂) concentrations. This is likely to have been effected by the PAM improving microbial conditions and partially being utilized as a substrate, with the latter being indicated by a PAM‐induced significant increase in the metabolic quotient. PAM did not reduce the microbial biomass except in one treatment at the highest application rate. Ammonium sulphate stimulated nitrification and reduced microbial biomass; the resultant acidification of the former is likely to have caused these effects. N fertilizer application may also have induced short‐term C‐limitation in the soil with impacts on microbial growth and respiration. The nitrification inhibitor DCD reduced the negative impacts on microbial biomass of (NH₄)₂SO₄ and proved to be an effective soil amendment to reduce nitrification under conditions where mineralization was increased by addition of PAM.     

FORMATION OF MICROBIAL BIOMASS DURING THE DECOMPOSITION OF 14C LABELLED RYEGRASS IN SOIL

Ryegrass uniformly labelled with ^I4C was incubated aerobically at 25°C for 62 days in two contrasting soils, a near-neutral (pH 6.8) palcudalf from England and a strongly acid (pH 3.6) haplorthox from Brazil. Decomposition of the labelled plant material was faster in the near-neutral soil throughout the whole of the incubation period. In neither soil did the addition of fresh plant material significantly accelerate the evolution of CO₂ from organic matter already in the soil, i.e. there was no priming action. In the near-neutral soil there was a rapid build up of labelled microbial biomass in the first 6 days, followed by a much slower increase that continued throughout the whole incubation period. After 62 days 22.5% of the labelled C remaining in the near-neutral soil was in the biomass. The yield coefficient (the fraction of the incoming plant C converted to microbial C) of this stabilized or ‘resting’ biomass was 0.15. Much less labelled microbial biomass was formed in the acid soil than in the near-neutral soil. By the end of 62 days only 6.2% of the labelled carbon remaining in the acid soil was in the biomass. Biomass C measurements in strongly acid soils must however be treated with caution as the technique used has not yet been adequately validated for such soils.     

Soluble organic nitrogen in temperate forest soils

Very few studies have been related to soluble organic nitrogen (SON) in forest soils. However, this nitrogen pool could be a sensitive indicator to evaluate the soil nitrogen status. The current study was conducted in temperate forests of Thuringia, Germany, where soils had SON (extracted in 0.5 M K₂SO₄) varying from 0.3 to 2.2% of total N, which was about one-third of the soil microbial biomass N by CFE. SON in study soils were positively correlated to microbial biomass N and soil total N. Multiple regression analysis also showed that mineral N negatively affected SON pool. The dynamics of the SON was significantly affected by mineralization and immobilization. During the 2 months of aerobic incubation, the SON were significantly correlated with net N mineralization and microbial biomass N. SON extracted by two different salt solution (i.e. 1 M KCl and 0.5 M K₂SO₄₎ were highly correlated. In mineral soil, SON concentrations extracted by 1 M KCl and 0.5 M K₂SO₄ solutions were similar. In contrast, in organic soil layer the amount of KCl-extractable SON was about 1.2-1.4 times higher than the K₂SO₄-extractable SON. Further studies such as the differences of organic N form and pool size between SON and dissolved organic N (DON) are recommended.     

Determination and use of a corrected control factor in the chloroform fumigation method of estimating soil microbial biomass

Estimates of soil microbial biomass are important for both comparative system analysis and mechanistic models. The method for measuring microbial biomass that dominates the literature is the chloroform fumigation incubation method (CFIM), developed on the premise that killed microorganisms are readily mineralized to CO₂, which is a measure of the initial population. Factors that effect the CFIM have been thoroughly investigated over the last 15 years. A question that still remains after countless experiments is the use of an appropriate nonfumigated control for accounting for native soil organic matter (SOM) mineralization during incubation. Our approach was to add hot-water-leached ¹⁴C-labeled straw to both fumigated and nonfumigated samples assuming the straw would mimic a recalcitrant C substrate fraction of SOM. The ratio of the ¹⁴C evolved from the fumigated sample over the ¹⁴C evolved from the control sample would provide a corrected control value to be used in calculating microbial biomass. This experiment was conducted on soils from forest, agricultural, grassland and shrub-steppe ecosystems. The results clearly indicate that equal recalcitrant C mineralization during incubation is not a valid assumption. The results with these soils indicate than on the average only 20% of the control CO₂ should be subtracted from the fumigated CO₂ for the biomass calculation. The correction value ranged from 18% for agricultural soils to 25% for shrub-steppe soil, with the average correction value being 20%. Our experiments show that corrected biomass values will be 1.5–2 times greater than uncorrected biomass values. In addition using a corrected control improved the 1:1 correlation between the CFIM and SIR methods for these soils.     

Compaction effects on CO2 and N2O production during drying and rewetting of soil

The effects of compaction on soil porosity and soil water relations are likely to influence substrate availability and microbial activity under fluctuating soil moisture conditions. We conducted a short laboratory incubation to investigate the effects of soil compaction on substrate availability and biogenic gas (CO₂ and N₂O) production during the drying and rewetting of a fine-loamy soil. Prior to initiating the drying and wetting treatments, CO₂ production (−10 kPa soil water content) from uncompacted soil was 2.3 times that of compacted soil and corresponded with higher concentrations of microbial biomass C (MBC) and dissolved organic C (DOC). In contrast, N₂O production was 67 times higher in compacted than uncompacted soil at field capacity. Soil aeration rather than substrate availability (e.g. NO₃⁻ and DOC) appeared to be the most important factor affecting N₂O production during this phase. The drying of compacted soil resulted in an initial increase in CO₂ production and a nearly two-fold higher average rate of C mineralization at maximum dryness (owing to a higher water-filled pore space [WFPS]) compared to uncompacted soil. During the drying phase, N₂O production was markedly reduced (by 93-96%) in both soils, though total N₂O production remained slightly higher in compacted than uncompacted soil. The increase in CO₂ production during the first 24 h following rewetting of dry soil was about 2.5 times higher in uncompacted soil and corresponded with a much greater release of DOC than in compacted soil. MBC appeared to be the source of the DOC released from uncompacted soil but not from compacted soil. The production of N₂O during the first 24 h following rewetting of dry soil was nearly 20 times higher in compacted than uncompacted soil. Our results suggest that N₂O production from compacted soil was primarily the result of denitrification, which was limited by substrates (especially NO₃⁻) made available during drying and rewetting and occurred rapidly after the onset of anoxic conditions during the rewetting phase. In contrast, N₂O production from uncompacted soil appeared to be primarily the product of nitrification that was largely associated with an accumulation of NO₃⁻ following rewetting of dry soil. Irrespective of compaction, the response to drying and rewetting was greater for N₂O production than for CO₂ production.     

Relationships of soil respiration to microbial biomass, substrate availability and clay content

The roles of microbial biomass (MBC) and substrate supply as well as their interaction with clay content in determining soil respiration rate were studied using a range of soils with contrasting properties. Total organic C (TOC), water-soluble organic carbon, 0.5 M K₂SO₄-extractable organic C and 33.3 mM KMnO₄-oxidisable organic carbon were determined as C availability indices. For air-dried soils, these indices showed close relationship with flush of CO₂ production following rewetting of the soils. In comparison, MBC determined with the chloroform fumigation-extraction technique had relatively weaker correlation with soil respiration rate. After 7 d pre-incubation, soil respiration was still closely correlated with the C availability indices in the pre-incubated soils, but poorly correlated with MBC determined with three different techniques—chloroform fumigation extraction, substrate-induced respiration, and chloroform fumigation-incubation methods. Results of multiple regression analyses, together with the above observations, suggested that soil respiration under favourable temperature and moisture conditions was principally determined by substrate supply rather than by the pool size of MBC. The specific respiratory activity of microorganisms (CO₂-C/MBC) following rewetting of air-dried soils or after 7 d pre-incubation was positively correlated with substrate availability, but negatively correlated with microbial pool size. Clay content had no significant effect on CO₂ production rate, relative C mineralization rate (CO₂-C/TOC) and specific respiratory activity of MBC during the first week incubation of rewetted dry soils. However, significant protective effect of clay on C mineralization was shown for the pre-incubated soils. These results suggested that the protective effect of clay on soil organic matter decomposition became significant as the substrate supply and microbial demand approached to an equilibrium state. Thereafter, soil respiration would be dependent on the replenishment of the labile substrate from the bulk organic C pool.     

Role of soil drying in nitrogen mineralization and microbial community function in semi-arid grasslands of north-west Australia

We examined effects of wetting and then progressive drying on nitrogen (N) mineralization rates and microbial community composition, biomass and activity of soils from spinifex (Triodia R. Br.) grasslands of the semi-arid Pilbara region of northern Australia. We compared soils under and between spinifex hummocks and also examined impacts of fire history on soils over a 28 d laboratory incubation. Soil water potentials were initially adjusted to −100 kPa and monitored as soils dried. We estimated N mineralization by measuring changes in amounts of nitrate (NO₃⁻-N) and ammonium (NH₄⁺-N) over time and with change in soil water potential. Microbial activity was assessed by amounts of CO₂ respired. Phospholipid fatty acid (PLFA) analyses were used to characterize shifts in microbial community composition during soil drying. Net N mineralized under hummocks was twice that of open spaces between hummocks and mineralization rates followed first-order kinetics. An initial N mineralization flush following re-wetting accounted for more than 90% of the total amount of N mineralized during the incubation. Initial microbial biomass under hummocks was twice that of open areas between hummocks, but after 28 d microbial biomass was<2 μ g⁻¹ ninhydrin N regardless of position. Respiration of CO₂ from soils under hummocks was more than double that of soils from between hummocks. N mineralization, microbial biomass and microbial activity were negligible once soils had dried to −1000 kPa. Microbial community composition was also significantly different between 0 and 28 d of the incubation but was not influenced by burning treatment or position. Regression analysis showed that soil water potential, microbial biomass N, NO₃⁻-N, % C and δ¹⁵N all explained significant proportions of the variance in microbial community composition when modelled individually. However, sequential multiple regression analysis determined only microbial biomass was significant in explaining variance of microbial community compositions. Nitrogen mineralization rates and microbial biomass did not differ between burned and unburned sites suggesting that any effects of fire are mostly short-lived. We conclude that the highly labile nature of much of soil organic N in these semi-arid grasslands provides a ready substrate for N mineralization. However, process rates are likely to be primarily limited by the amount of substrate available as well as water availability and less so by substrate quality or microbial community composition.     

Gross fluxes of nitrogen in grassland soil exposed to elevated atmospheric pCO2 for seven years

Plant response to increasing atmospheric CO₂ partial pressure (pCO₂) depends on several factors, one of which is mineral nitrogen availability facilitated by the mineralisation of organic N. Gross rates of N mineralisation were examined in grassland soils exposed to ambient (36 Pa) and elevated (60 Pa) atmospheric pCO₂ for 7 years in the Swiss Free Air Carbon dioxide Enrichment experiment. It was hypothesized that increased below-ground translocation of photoassimilates at elevated pCO₂ would lead to an increase in immobilisation of N due to an excess supply of energy to the roots and rhizosphere. Intact soil cores were sampled from Lolium perenne and Trifolium repens swards in May and September, 2000. The rates of gross N mineralisation (m) and NH₄⁺ consumption (c) were determined using ¹⁵N isotopic dilution during a 51-h period of incubation. The rates of N immobilisation were estimated either as the difference between m and the net N mineralisation rate or as the amount of ¹⁵N released from the microbial biomass after chloroform fumigation. Soil samples from both swards showed that the rates of gross N mineralisation and NH₄⁺ consumption did not change significantly under elevated pCO₂. The lack of a significant effect of elevated pCO₂ on organic N turnover was consistent with the similar size of the microbial biomass and similar immobilisation of applied ¹⁵N in the microbial N pool under ambient and elevated pCO₂. Rates of m and c, and microbial ¹⁵N did not differ significantly between the two sward types although a weak (p<0.1) pCO₂ by sward interaction occurred. A significantly larger amount of NO₃⁻ was recovered at the end of the incubation in soil taken from T. repens swards compared to that from L. perenne swards. Eleven percent of the added ¹⁵N were recovered in the roots in the cores sampled under L. perenne, while only 5% were recovered in roots of T. repens. These results demonstrate that roots remained a considerable sink despite the shoots being cut at ground level prior to incubation and suggest that the calculation of N immobilisation from gross and net rates of mineralisation in soils with a high root biomass does not reflect the actual immobilisation of N in the microbial biomass. The results of this study did not support the initial hypothesis and indicate that below-ground turnover of N, as well as N availability, measured in short-term experiments are not strongly affected by long-term exposure to elevated pCO₂. It is suggested that differences in plant N demand, rather than major changes in soil N mineralisation/immobilisation, are the long-term driving factors for N dynamics in these grassland systems.