Is CO2 evolution in saline soils affected by an osmotic effect and calcium carbonate?

Salt-affected soils are widespread, particularly in arid climates, but information on nutrient dynamics and carbon dioxide (CO₂) efflux from salt-affected soils is scarce. Four laboratory incubation experiments were conducted with three soils. To determine the influence of calcium carbonate (CaCO₃) on respiration in saline and non-saline soils, a loamy sand (6.3% clay) was left unamended or amended with NaCl to obtain an electrical conductivity (EC) of 1.0 dS?m^?1 in a 1:5 soil/water extract. Powdered CaCO₃ at rates of 0%, 0.5%, 1.0%, 2.5%, 5.0% and 10.0% (w/w) and 0.25-2 mm mature wheat residue at 0% and 2% (w/w) were then added. Cumulative CO₂-C emission from the salt amended and unamended soils was not affected by CaCO₃ addition. To investigate the effect of EC on microbial activity, soil respiration was measured after amending a sandy loam (18.8% clay) and a silt loam (22.5% clay) with varying amount of NaCl to obtain an EC_1:5 of 1.0–8.0 dS?m^?1 and 2.5 g glucose C?kg^?1 soil. Soil respiration was reduced by more than 50% at EC_1:5?≥?5.0 dS?m^?1. In a further experiment, salinity up to an EC_1:5 of 5.0 dS?m^?1 was developed in the silt loam with NaCl or CaCl₂. No differences in respiration at a given EC were obtained between the two salts, indicating that Na and Ca did not differ in toxicity to microbial activity. The effect of different addition rates (0.25–2.0%) of mature wheat residue on the response of respiration to salinity was investigated by adding NaCl to the silt loam to obtain an EC_1:5 of 2.0 and 4.0 dS?m^?1. The clearest difference between salinity levels was with 2% residue rate. At a given salinity level, the modelled decomposition constant ‘k’ increased with increasing residue addition rate up to 1% and then remained constant. Particulate organic carbon left after decomposition from the added wheat residues was negatively correlated with cumulative respiration but positively correlated with EC. Inorganic N (NH ₄ ⁺ -N and NO ₃ ^? -N) and resin P significantly decreased with increasing salinity. Resin P was significantly decreased by addition of CaCl₂ and CaCO₃.     

镁碱化盐土微生物生物量和土壤基础呼吸

通过测定甘肃河西走廊疏勒河中游昌马冲积扇缘不同镁碱度条件下10个采样点30个土样的化学性质和生物化学性质指标,研究了电导率和镁碱度对土壤微生物生物量及其基础呼吸的影响。结果表明:微生物生物量碳(氮)和土壤基础呼吸与电导率、镁碱度和Mg2+/Ca2+之间显著负相关,表明盐度和镁碱度对土壤微生物群落有显著的抑制作用,而且盐度的抑制作用比镁碱度更大;微生物代谢熵(qCO2)和电导率、镁碱度、Mg2+/Ca2+之间为正相关关系,也说明镁碱化盐土对土壤微生物而言是一种严重的胁迫环境。     

A method for determining microbially available N and P in an organic soil

Summary A bioassay of microbially available soil N and P is described. It is based on the addition of glucose together with N or P to soil, followed by monitoring of the respiration rate. The addition of glucose + N resulted in an immediate increase in the soil respiration rate followed by a short period of exponential increase, reflecting the growth of microorganisms on the added substrate. The exponential phase levelled off, when lack of P prevented further growth of the soil microorganisms. The soil respiration rate then remained constant for several hours before decreasing, when glucose became limiting. The addition of glucose + P resulted in a lower plateau of the soil respiration rate, indicating that microbial growth was more limited by N than P in this forest soil (0.28 and 0.79 mg CO₂ g^-1 organic matter h^-1, respectively). Additions of the limiting nutrient resulted in a proportional increase in the constant level of the soil respiration rate. This was used to calculated the increase in the soil respiration rate per mg N (0.71 mg CO₂ h^-1) or mg P (4.6 mg CO₂ h^-1) added to this particular soil. Microbially available N was then calculated in two ways from the regression equation (0.15 or 0.40 mg g^-1 organic matter) and P (0.13 or 0.17 mg g^-1 organic matter). A comparison with 2 M KCl extraction showed that in nutrient-poor forest soils the microbially available N was 6.3 or 18.5 times higher than the KCl extractable N.     

Salinity effects on carbon mineralization in soils of varying texture

In salt-affected soils, soil organic carbon (SOC) levels are usually low as a result of poor plant growth; additionally, decomposition of soil organic matter (SOM) may be negatively affected. Soil organic carbon models, such as the Rothamsted Carbon Model (RothC), that are used to estimate carbon dioxide (CO₂) emission and SOC stocks at various spatial scales, do not consider the effect of salinity on CO₂ emissions and may therefore over-estimate CO₂ release from saline soils. Two laboratory incubation experiments were conducted to assess the effect of soil texture on the response of CO₂ release to salinity, and to calculate a rate modifier for salinity to be introduced into the RothC model. The soils used were a sandy loam (18.7% clay) and a sandy clay loam (22.5% clay) in one experiment and a loamy sand (6.3% clay) and a clay (42% clay) in another experiment. The water content was adjusted to 75%, 55%, 50% and 45% water holding capacity (WHC) for the loamy sand, sandy loam, sandy clay loam and the clay, respectively to ensure optimal soil moisture for decomposition. Sodium chloride (NaCl) was used to develop a range of salinities: electrical conductivity of the 1:5 soil: water extract (EC_1:5) 1, 2, 3, 4 and 5 dS m⁻¹. The soils were amended with 2% (w/w) wheat residues and CO₂ emission was measured over 4 months. Carbon dioxide release was also measured from five salt-affected soils from the field for model evaluation. In all soils, cumulative CO₂-C g⁻¹ soil significantly decreased with increasing EC_1:5 developed by addition of NaCl, but the relative decrease differed among the soils. In the salt-amended soils, the reduction in normalised cumulative respiration (in percentage for the control) at EC_1:5 > 1.0 dS m⁻¹ was most pronounced in the loamy sand. This is due to the differential water content of the soils, at the same EC_1:5; the salt concentration in the soil solution is higher in the coarser textured soils than in fine textured soils because in the former soils, the water content for optimal decomposition is lower. When salinity was expressed as osmotic potential, the decrease in normalised cumulative respiration with increasing salinity was less than with EC_1:5. The osmotic potential of the soil solution is a more appropriate parameter for estimating the salinity effect on microbial activity than the electrical conductivity (EC) because osmotic potential, unlike EC, takes account into salt concentration in the soil solution as a function of the water content. The decrease in particulate organic carbon (POC) was smaller in soils with low osmotic potential whereas total organic carbon, humus-C and charcoal-C did not change over time, and were not significantly affected by salinity. The modelling of cumulative respiration data using a two compartment model showed that the decomposition of labile carbon (C) pool is more sensitive to salinity than that of the slow C pool. The evaluation of RothC, modified to include the decomposition rate modifier for salinity developed from the salt-amended soils, against saline soils from the field, suggested that salinity had a greater effect on cumulative respiration in the salt-amended soils. The results of this study show (i) salinity needs to be taken into account when modelling CO₂ release and SOC turnover in salt-affected soils, and (ii) a decomposition rate modifier developed from salt-amended soils may overestimate the effect of salinity on CO₂ release.     

Net nitrogen immobilization in soil induced by small additions of energy sources

Abstract

This study investigated whether small additions to soil of primary paper-mill sludge, a wood fibre residue from paper production (fibre sludge), caused temporary N immobilization and thereby reduced the amount of inorganic nitrogen leached from agricultural land. This was achieved by measuring respiration and immobilization of N in incubation studies at 8°C, with fibre sludge added at rates varying from 63 to 1000?mg?C?kg^?1 soil. Glucose added at rates of 63–250?mg?C?kg^?1 soil was used as a reference. Respiration in soil after glucose addition followed an exponential course with the highest rates on days 2–4. During this period maximum peaks of net N immobilization were measured. Even addition of only 63?mg glucose-C?kg^?1 soil caused significant immobilization of N in soil. Fibre sludge additions to soil caused lower respiration activities, characterized by two initial peaks followed by somewhat higher respiration rates during the remaining incubation than for glucose. It was likely that hemicellulose, which amounted to 14% of the total C, was the initial available energy source in the sludge as concentrations of water-soluble C were very low. Addition of at least 250?mg?C?kg^?1 soil as fibre sludge was required to cause significant N immobilization in soil corresponding to 5?kg?N?ha^?1. Both nitrate and ammonium were immobilized. Relating maximum N immobilization data during days 2 to 10 to corresponding respiration data for glucose and fibre sludge revealed that microbes utilised similar amounts of C per unit N immobilized. On average, 175.6±74.8?mg CO₂-C were respired to immobilize 1?mg?N and the relationship between C respiration and N immobilization was linear (R ²=0.984). To make soil application of fibre sludge a realistic counter-measure against N leaching from agricultural soils, pre-treatment is necessary to increase the content of energy readily available to microbes.     

Carbon turnover in the rhizosphere under continuous plant labeling with <Superscript>13</Superscript>CO<Subscript>2</Subscript>: Partitioning of root,microbial, and rhizomicrobial respiration

The input of labeled C into the pool of soil organic matter, the CO₂ fluxes from the soil, and the contribution of root and microbial respiration to the CO₂ emission were studied in a greenhouse experiment with continuous labeling of oat plants with ¹³CO₂ using the method of the natural ¹³C abundance in the air. The carbon of the microbial biomass composed 56 and 39% of the total amounts of ¹³C photoassimilates in the rhizosphere and in the bulk soil, respectively. The contribution of root respiration to the CO₂ emission from the soil reached 61–92%, including 4–23% of the rhizomicrobial respiration. The contribution of the microbial respiration to the total CO₂ emission from the soil varied from 8 to 39%. The soil organic matter served as the major carbon-containing substrate for microorganisms in the bulk soil and in the rhizosphere: 81–91% of the total amount of carbon involved in the microbial metabolism was derived from the soil organic matter.     

Application of mixed straw and biochar meets plant demand of carbon dioxide and increases soil carbon storage in sunken solar greenhouse vegetable production

Solar vegetable greenhouse soils show low soil organic carbon content and thus also low rates of soil respiration. Processing vegetable residues to biochar and mixing biochar with maize straw might improve soil respiration and increase soil organic carbon stocks, while preventing the spread of soil-borne diseases carried by vegetable residues. In an incubation experiment, we tested how additions of maize straw (S) and biochar (B) added in varying ratios (100S, 75S25B, 50S50B, 25S75B, 100B and 0S0B (control)) affect soil respiration and fraction of added C remaining in soil. Daily CO₂ emissions were measured over 60 days incubation, the natural abundance of ¹³C in soil and in the added biochar and maize straw were analysed. Our result shows that (a) soil CO₂ emissions were significantly increased compared to soil without the straw additions, while addition of biochar only decreased soil respiration; (b) cumulative CO₂ emissions decreased with increasing ratio of added biochar to maize straw; (c) the abundance of soil ¹³C was significant positively correlated with cumulative CO₂ emissions, and thus with the ratio of straw addition. Our results indicate that incorporation of maize straw in greenhouse soils is a meaningful measure to increase soil respiration and to facilitate greenhouse atmosphere CO₂ limitation while producing vegetables. On the other hand, additions of biochar from vegetable residues will increase soil organic carbon concentration. Therefore, the simultaneous application of maize straw and biochar obtained from vegetable residues is an effective option to maintain essential soil functions for vegetable production in sunken solar greenhouses.     

Soil carbon dioxide emission from intensively cultivated black soil in Northeast China: nitrogen fertilization effect

Purpose

The aim of this study was to understand the effect of nitrogen fertilization on soil respiration and native soil organic carbon (SOC) decomposition and to identify the key factor affecting soil respiration in a cultivated black soil.

Materials and methods

A field experiment was conducted at the Harbin State Key Agroecological Experimental Station, China. The study consisted of four treatments: unplanted and N-unfertilized soil (U0), unplanted soil treated with 225?kg?N?ha^?1 (UN), maize planted and N-unfertilized soil (P0), and planted soil fertilized with 225?kg?N?ha^?1 (PN). Soil CO₂ and N₂O fluxes were measured using the static closed chamber method.

Results and discussion

Cumulative CO₂ emissions during the maize growing season with the U0, UN, P0, and PN treatments were 1.29, 1.04, 2.30 and 2.27?Mg?C?ha^?1, respectively, indicating that N fertilization significantly reduced the decomposition of native SOC. However, no marked effect on soil respiration in planted soil was observed because the increase of rhizosphere respiration caused by N addition was counteracted by the reduction of native SOC decomposition. Soil CO₂ fluxes were significantly affected by soil temperature but not by soil moisture. The temperature sensitivity (Q ₁₀) of soil respiration was 2.16?C2.47 for unplanted soil but increased to 3.16?C3.44 in planted soil. N addition reduced the Q ₁₀ of native SOC decomposition possibly due to low labile organic C but increased the Q ₁₀ of soil respiration due to the stimulation of maize growth. The estimated annual CO₂ emission in N-fertilized soil was 1.28?Mg?C?ha^?1 and was replenished by the residual stubble, roots, and exudates. In contrast, the lost C (1.53?Mg?C?ha^?1) in N-unfertilized soil was not completely supplemented by maize residues, resulting in a reduction of SOC. Although N fertilization significantly increased N₂O emissions, the global warming potential of N₂O and CO₂ emissions in N-fertilized soil was significantly lower than in N-unfertilized soil.

Conclusions

The stimulatory or inhibitory effect of N fertilization on soil respiration and basal respiration may depend on labile organic C concentration in soil. The inhibitory effect of N fertilization on native SOC decomposition was mainly associated with low labile organic C in tested black soil. N application could reduce the global warming potential of CO₂ and N₂O emissions in black soil.     

Heterotrophy-coordinated diazotrophy is associated with significant changes of rare taxa in soil microbiome

Soil heterotrophic respiration during decomposition of carbon (C)-rich organic matter plays a vital role in sustaining soil fertility. However, it remains poorly understood whether dinitrogen (N₂) fixation occurs in support of soil heterotrophic respiration. In this study, ¹⁵N₂-tracing indicated that strong N₂ fixation occurred during heterotrophic respiration of carbon-rich glucose. Soil organic ¹⁵N increased from 0.37 atom% to 2.50 atom% under aerobic conditions and to 4.23 atom% under anaerobic conditions, while the concomitant CO₂ flux increased by 12.0-fold under aerobic conditions and 5.18-fold under anaerobic conditions. Soil N₂ fixation was completely absent in soils replete with inorganic N, although soil N bioavailability did not alter soil respiration. High-throughput sequencing of the 16S rRNA gene further indicated that: i) under aerobic conditions, only 15.2% of soil microbiome responded positively to glucose addition, and these responses were significantly associated with soil respiration and N₂ fixation and ii) under anaerobic conditions, the percentage of responses was even lower at 5.70%. Intriguingly, more than 95% of these responses were originally rare with < 0.5% relative abundance in background soils, including typical N₂-fixing heterotrophs such as Azotobacter and Clostridium and well-recognized non-N₂-fixing heterotrophs such as Sporosarcina, Agromyces, and Sedimentibacter. These results suggest that only a small portion of the soil microbiome could respond quickly to the amendment of readily accessible organic C in a fluvo-aquic soil and highlighted that rare phylotypes might have played more important roles than previously appreciated in catalyzing soil C and nitrogen turnovers. Our study indicates that N₂ fixation could be closely associated with microbial turnover of soil organic C when available in excess.     

Microbial biomass and activity in alkalized magnesic soils under arid conditions

The effects of salinity and Mg²⁺ alkalinity on the size and activity of the soil microbial communities were investigated. The study was conducted along the border area of the alluvial fan of the Taolai River. Thirty soil samples were taken which had an electrical conductivity (EC) gradient of 0.93-29.60 mS cm⁻¹. Soil pH ranged from 8.60 to 9.33 and correlated positively with Mg²⁺/Ca²⁺ ratio, exchangeable Mg²⁺ percentage and HCO₃⁻+CO₃²⁻. Mg²⁺/Ca²⁺ varied considerably from 3.04 to 61.31, with an average of 23.03. Exchangeable Mg²⁺ percentage generally exceeded 60% and had a positive correlation with Mg²⁺/Ca²⁺. HCO₃⁻+CO₃²⁻ averaged 1.63 cmol kg⁻¹ and usually did not exceed 2.0 cmol kg⁻¹.Microbial biomass, indices of microbial activity and the activities of the hydrolases negatively correlated with Mg²⁺/Ca²⁺ or exchangeable Mg²⁺ percentage. Biomass C, biomass N, microbial quotient (the percentage of soil organic C present as biomass C), biomass N as a percentage of total N, potentially mineralizable N, FDA hydrolysis rate and arginine ammonification rate decreased exponentially with increasing EC. The biomass C/N tended to be lower in soils with higher salinity and Mg²⁺ alkalinity, probably reflecting the bacterial dominance in microbial biomass in alkalized magnesic soils. The metabolic quotient (qCO₂) positively correlated with salinity and Mg²⁺ alkalinity, and showed a quadratic relationship with EC, indicating that increasing salinity and Mg²⁺ alkalinity resulted in a progressively smaller, more stressed microbial communities which was less metabolically efficient. Consequently, our data suggest that salinity and Mg²⁺ alkalinity are stressful environments for soil microorganisms.     

Impacts of trace amounts of labile C on plant N limitation vary from hour to week timescales

The ability of terrestrial ecosystems to store carbon (C) under rising atmospheric CO₂ will depend on how severely nitrogen (N) will limit plant growth. We tested whether increased C availability in the soil at elevated CO₂ could affect N limitation by inducing N release from soil organic matter (SOM). We established microcosms composed of Holcus lanatus plants, field soil (containing “old” SOM) and ¹⁵?N-labeled plant litter (representing “new” SOM), simulated different levels of root C release by adding a single pulse of 0, 18, 44, or 175?μg glucose C?g^?1 dry soil and recorded the effects on soil microbial biomass, microbial-feeding protozoa and nematodes and plant performance 1, 3, 9, and 32?days after C addition. The effects on H. lanatus growth and N uptake depended on the amount of added C and the time elapsed since addition. Shoot N concentration and N content were higher in pots amended with 44?μg?C g^?1 soil than in other pots 1?day after C addition. Later, 9 and 32?days after C addition, the highest glucose addition reduced the dry mass, N concentration, and N content of H. lanatus shoots in comparison to other treatment levels. Microbial biomass was generally higher in soils subjected to 44?μg glucose C?g^?1 soil than in control soils, and, at the last harvest, the numbers of protozoa were significantly higher in all soils with glucose amendments than in control soils. No effects on microbial-feeding nematodes were found, and plant N uptake from “old” and “new” SOM was equally affected by C addition. Our results seem to suggest that, while a low pulse of labile C can increase plant N uptake temporarily on an hour scale, higher amounts of C will intensify plant N limitation at timescales of days and weeks. Generalization of such dose and time dependent results requires great caution, but if verified in other plant–soil systems as well, they would suggest that plant N availability under elevated C availability may depend on the balance between positive and negative effects operating at different timescales and triggered by additional C pulses of varying size.     

不同管理措施对滨海盐渍农田土壤CO2排放及碳平衡的影响

为探讨不同管理措施对滨海盐渍农田碳平衡的影响,本文通过玉米–小麦轮作试验,研究农田土壤的CO_2释放规律,及其农田碳收支状况。试验设计6个处理:1常规对照(CK);2有机肥常量(OF);3氮肥增施(NF);4秸秆还田(S);5有机肥加秸秆(OF+S);6免耕(NT)。研究表明,秸秆还田和有机肥的施用增加了土壤呼吸的强度,而免耕处理的CO_2平均释放量最低,不同处理下土壤呼吸总体表现为OF+SSOMNFCKNT。各处理土壤有机碳含量随着作物的收获逐渐升高,其中OF与NT增加最多,而增施氮肥处理并没有显著提高土壤的有机碳水平。各处理间的有机碳含量没有显著性差异。在两季作物种植结束后,各处理的碳输入均高于碳输出,均为碳净输入,表现出较强的碳汇特征。秸秆还田和单施有机肥的碳净输入均显著高于对照,可有效减缓因农田土壤CO_2排放而造成的全球气候变化问题。     

Einfluss der pflanzlichen rhizodeposition auf die c-flüsse im boden: Influence of plant rhizodeposition on c fluxes in soil

By means of ¹⁴C pulse labelling and sterilization of soil, a C release into soil of 14?–?18% of net CO₂ assimilation (corresponding to 23?–?26% of ¹⁴C incorporated in plant tissue) was observed during vegetation period (excluding root respiration). Microbial colonization increased this rhizodeposition. About 60?–?80% of the primary root-borne compounds were very quickly respirated by microorganisms (secondary respiration of exudates). Fourteen to 38% (corresponding to 130?–?400?kg C?ha^?1 a^?1) of the remaining rhizodeposites were located in a zone close to root surface (up to 5?mm). Their solubility in water decreased with increasing distance to the root. The fraction of water-soluble root exudates included primarily carbohydrates (sucrose, glucose, fructose, ribose), amino acids/amides (glutamine, serine, aspartic acid) as well as organic acids (citric, succinic and tartaric acids). The water-insoluble portion of rhizodeposites were strongly absorbed by soil clay-fraction and substantially increased stability of SOM and soil aggregates.     

Enzymatic activities and microbial communities in an Antarctic dry valley soil: Responses to C and N supplementation

The soils of the Antarctic dry valleys are exposed to extremely dry and cold conditions. Nevertheless, they contain small communities of micro-organisms that contribute to the biogeochemical transformations of the bioelements, albeit at slow rates. We have determined the dehydrogenase, β-glucosidase, acid and alkaline phosphatase and arylsulphatase activities and the rates of respiration (CO₂ production) in laboratory assays of soils collected from a field experiment in an Antarctic dry valley. The objective of the field experiment was to test the responses of the soil microbial community to additions of C and N in simple (glucose and NH₄Cl) and complex forms (glycine and lacustrine detritus from the adjacent lake comprising principally cyanobacterial necromass). The soil samples were taken 3 years after the experimental treatments had been applied. In unamended soil, all enzyme activities and respiration were detected indicating that the enzymatic capacity to mineralize organic C, P and S compounds existed in the soil, despite the very low organic matter content. Relative to the control (unamended soil), respiration was significantly increased by all the experimental additions of C and N except the smallest NH₄Cl addition (1 mg N g⁻¹ soil) and the smallest detritus addition (1.5 mg C g⁻¹ soil and 0.13 mg N g⁻¹ soil). The activities of all enzymes except dehydrogenase were increased by C and combined large C (10 mg C g⁻¹ soil) and N additions, but either unchanged or diminished by addition of either N only or N (up to 10 mg N g⁻¹ soil) with only small C (1 mg C g⁻¹ soil) additions in the form of glucose and NH₄Cl. This suggests that in the presence of a large amount of N, the C supply for enzyme biosynthesis was limited. When normalized with respect to soil respiration, only arylsulphatase per unit of respiration showed a significant increase with C and N additions as glucose and NH₄Cl, consistent with S limitation when C and N limitations have been alleviated. Based on the positive responses of enzyme activity, detritus appeared to provide either conditions or resources which led to a larger biological response than a similar amount of C and more N added in the form of defined compounds (glucose, NH₄Cl or glycine). Assessment of the soil microbial community by ester-linked fatty acid (ELFA) analysis provided no evidence of changes in the community structure as a result of the C and N supplementation treatments. Thus the respiration and enzyme activity responses to supplementation occurred in an apparently structurally stable or unresponsive microbial community.     

Reduction in CO2 emission from normal and saline soils amended with coal fly ash

Purpose

Fly ash can reduce CO₂ emission from soils via biochemical (i.e., inhibition of microbial activity) and physicochemical (i.e., carbonation) mechanisms. This study investigated the effects of fly ash amendment on biochemical and physicochemical reduction in CO₂ emission from normal and saline soils.

Materials and methods

The physicochemical mechanisms of reduction in CO₂ emission by fly ash were estimated in a batch experiment with carbonate solution as a CO₂ source by the scanning electron microscope (SEM) and inductively coupled plasma analyses. Biochemical mechanisms of reduction in CO₂ emission by fly ash were investigated in a 3-day laboratory incubation experiment with normal and saline soils in the absence and presence of fly ash. Finally, the effects of fly ash amendment at a variety rate from 2 to 15?% (w/w) on CO₂ emission from normal and saline soils in the presence of additional organic carbon source (glucose) were investigated through a 15-day laboratory incubation study.

Results and discussion

In the batch experiment with carbonate solution, both the SEM image of fly ash and changes in soluble Ca and Mg concentrations during reaction with carbonate suggested that the formation of CaCO₃ and MgCO₃ via carbonation was the principal physicochemical mechanism of carbonate removal by fly ash. In the 3-day incubation study conducted to examine biochemical mechanisms of reduction in CO₂ emission by fly ash, microbial respiration of saline soil was inhibited (P?<?0.05) by fly ash due to high pH, salinity, and boron concentration of fly ash; meanwhile, for normal soil, there was no inhibitory effect of fly ash on microbial respiration. In the 15-day incubation with glucose, fly ash application at a variety rates from 2 to 15?% (w/w) reduced CO₂ emission by 3.6 to 21.4?% for normal and by 19.8 to 30.3?% for saline soil compared to the control without fly ash. For saline soil, the reduction in CO₂ emission was attributed primarily to inhibition of microbial respiration by fly ash; however, for normal soil in which suppression of microbial respiration by fly ash was not apparent, carbonation was believed to play an important role in reduction of CO₂ emission.

Conclusions

Therefore, fly ash may be helpful in reducing CO₂ emission from normal soils via carbonation. For saline soil, however, fly ash needs to be carefully considered as a soil amendment to reduce CO₂ emission as it can inhibit soil microbial activities and thus degrade soil quality.     

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.     

Decoupling of microbial glucose uptake and mineralization in soil

The rate of organic matter turnover in soil is a critical component of the terrestrial carbon cycle and is frequently estimated from measurements of respiration. For estimates to be reliable requires that isotopically labelled substrate uptake into the soil microbial biomass and its subsequent mineralization occurs almost simultaneously (i.e. no time delay). Here we investigated this paradigm using glucose added to an agricultural soil. Immediately after collection from the field, various concentrations of ¹⁴C-labeled glucose (1 μM to 10 mM) were added to soil and the depletion from the soil solution measured at 1–60 min after substrate addition. ¹⁴CO₂ production from the mineralization of glucose was simultaneously measured. The microbial uptake of glucose from soil solution was concentration-dependent and kinetic analysis suggests the operation of at least two distinct glucose transport systems of differing affinity. At glucose concentrations reflecting those naturally present in the soil solution (54±10 μM), the half-time (t_1/2) of exogenous glucose was extremely rapid at ca. 30 s. At higher glucose concentrations (100 μM to 10 mM), the t_1/2 values for the high-affinity carrier were altered little, but increasing proportions of glucose were taken up by the low affinity transport system. Glucose mineralization by the soil microbial community showed a significant delay after its uptake into the microbial biomass suggesting a decoupling of glucose uptake and subsequent respiration, possibly by dilution of glucose in labile metabolite pools. By fitting a double first order kinetic equation to the mineralization results we estimated the t_1/2 for the first rapid phase of respiration at natural soil solution glucose concentrations to be 6–8 min, but at least 87% of the added glucose was retained in the microbial biomass prior to mineralization. Our results suggest that in this soil the soil solution glucose pool turns over 100–1000 times each day, an order of magnitude faster than when determined from measurements of mineralization. These results imply that traditional isotopic based measurements of substrate turnover measured using CO₂ may vastly underestimate their rate of cycling in soil.     

The response of organic matter mineralisation to nutrient and substrate additions in sub-arctic soils

Global warming in the Arctic may alter decomposition rates in Arctic soils and therefore nutrient availability. In addition, changes in the length of the growing season may increase plant productivity and the rate of labile C input below ground. We carried out an experiment in which inorganic nutrients (NH₄NO₃ and NaPO₄) and organic substrates (glucose and glycine) were added to soils sampled from across the mountain birch forest-tundra heath ecotone in northern Sweden (organic and mineral soils from the forest, and organic soil only from the heath). Carbon dioxide production was then monitored continuously over the following 19 days. Neither inorganic N nor P additions substantially affected soil respiration rates when added separately. However, combined N and P additions stimulated microbial activity, with the response being greatest in the birch forest mineral soil (57% increase in CO₂ production compared with 26% in the heath soil and 8% in the birch forest organic soil). Therefore, mineralisation rates in these soils may be stimulated if the overall nutrient availability to microbes increases in response to global change, but N deposition alone is unlikely to enhance decomposition. Adding either, or both, glucose and glycine increased microbial respiration. Isotopic separation indicated that the mineralisation of native soil organic matter (SOM) was stimulated by glucose addition in the heath soil and the forest mineral soil, but not in the forest organic soil. These positive ‘priming’ effects were lost following N addition in forest mineral soil, and following both N and P additions in the heath soil. In order to meet enhanced microbial nutrient demand, increased inputs of labile C from plants could stimulate the mineralisation of SOM, with the soil C stocks in the tundra-heath potentially most vulnerable.     

Respiration of Louisiana Freshwater Floating Marsh Soils Amended with Ammonium,Phosphate, and Sulfate

Wetland soils of the freshwater coastal deltaic regions of Louisiana have developed under decreasing influence from the Mississippi River, which has resulted in lower available nutrient conditions and sediment input relative to other coastal marshes. A laboratory soil respiration experiment was conducted to measure cumulative carbon dioxide (CO₂) and methane (CH₄) production in soils from a floating freshwater marsh in response to additions of added ammonium (N), phosphate (P), ammonium (N) + phosphate (P), and sulfate (S). CO₂ respiration was significantly greater over a 28-day period than controls following ammonium N, phosphorus, and sulfate addition at 10 mg L^?1. Nitrogen and phosphorus addition at 10 mg L^?1 also increased methane production. The lower sulfate amendment (10 mg L^?1) did not significantly increase CH₄ production. In contrast, the greatest sulfate treatment (100 m l^?1) significantly reduced total carbon (C) production by inhibiting CH₄ production. The fact that soil C/N (20.2) and C/P (355) ratios were both relatively low may partially explain why both N and P colimited microbial activity and respiration. While microbial activity of freshwater floating marsh soils was stimulated over the short term with increased ammonium, nitrogen, phosphorus, and sulfate exposure, it is unclear whether the increase would be the same over extended periods or would increase in plant productivity from nutrient additions compensate for any loss in soil carbon.     

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。