Addition of a clay subsoil to a sandy topsoil changes the response of microbial activity to drying and rewetting after residue addition – a model experiment

The effect of drying and rewetting (DRW) on C mineralization has been studied extensively but mostly in absence of freshly added residues. But in agricultural soils large amounts of residues can be present after harvest; therefore, the impact of DRW in soil after residue addition is of interest. Further, sandy soils may be ameliorated by adding clay‐rich subsoil which could change the response of microbes to DRW. The aim of this study was to investigate the effect of DRW on microbial activity and growth in soils that were modified by mixing clay subsoil into sandy top soil and wheat residues were added. We conducted an incubation experiment by mixing finely ground wheat residue (20 g kg^–1) into top loamy sand soil with clay‐rich subsoil at 0, 5, 10, 20, 30, and 40% (w/w). At each clay addition rate, two moisture treatments were imposed: constantly moist control (CM) at 75% WHC or dry and rewet. Soil respiration was measured continuously, and microbial biomass C (MBC) was determined on day 5 (before drying), when the soil was dried, after 5 d dry, and 5 d after rewetting. In the constantly moist treatment, increasing addition rate of clay subsoil decreased cumulative respiration per g soil, but had no effect on cumulative respiration per g total organic C (TOC), indicating that the lower respiration with clay subsoil was due to the low TOC content of the sand‐clay mixes. Clay subsoil addition did not affect the MBC concentration per g TOC but reduced the concentration of K₂SO₄ extractable C per g TOC. In the DRW treatment, cumulative respiration per g TOC during the dry phase increased with increasing clay subsoil addition rate. Rewetting of dry soil caused a flush of respiration in all soils but cumulative respiration at the end of the experiment remained lower than in the constantly moist soils. Respiration rates after rewetting were higher than at the corresponding days in constantly moist soils only at clay subsoil addition rates of 20 to 40%. We conclude that in presence of residues, addition of clay subsoil to a sandy top soil improves microbial activity during the dry phase and upon rewetting but has little effect on microbial biomass.     

Enhancing Soil Quality through Residue Management in a Rice-Wheat System in Fukuoka,Japan

A long-term experiment (LTE) on a rice-wheat system was initiated in 1963 at the Kyushu National Agricultural Experiment Station, in Fukuoka, Japan, to determine the effects of continuous application of rye grass/wheat straw, rice straw and rice straw compost, alone or in combination with inorganic N on crop yields. Increase in rice yields and enhancement of total soil C and N contents with the application of organic residues in this LTE have been reported earlier. However, evaluation of the changes in the soil microbiological properties and the decomposable C fraction of soil organic matter that is needed for soil quality assessment is still lacking. Soil samples were collected after rice harvest in 2003 from the organic residue treatments and unfertilized control, air-dried and incubated for 1 month under aerobic [50% water-filled pore space (WFPS)] and flooded conditions prior to the analysis of the amount of microbial biomass C (MBC), soil respiration and the amount of potential mineralizable N (PMN). The contents of total C (TC), total N (TN), organic C (OC), hot water-extractable C (HWEC) and permanganate-oxidizable C (POC) were determined from air-dried soils. Organic residue incorporation brought about significant increases in the contents of TC, TN, OC, POC, HWEC and PMN. The largest accumulation of total C (23%) and N (72%) in the soil was from rice straw compost, compared with that from rice straw (C, 7% and N, 33%) and rye grass/wheat straw (C, 9% and N, 29%). Incorporation of rice straw compost also increased the amount of MBC under both aerobic and flooded conditions and basal soil respiration under aerobic conditions only. An efficient utilization of C by microorganisms was indicated by a significantly lower metabolic quotient (qCO₂) in the composted and uncomposted rice straw treatments compared with the control in the “-” N treatment under aerobic conditions. Similarly, the flush of CO₂ after rewetting of dry soil per unit of HWEC was lower in the organic matter treatments, indicating a more efficient C utilization and lower C losses per unit of available C. The content of HWEC was significantly correlated with the basal soil respiration (at 50% WFPS), the amounts of MBC, PMN and with the increase in the content of soil organic C in the residuetreated soils. In the treatments without inorganic N fertilizer, grain yield was significantly correlated with the amounts of total organic C, HWEC, MBC (at 50% WFPS), basal soil respiration (at 50% WFPS) and the amount of PMN.     

Microbial biomass dynamics in recently air-dried and rewetted soils compared to others stored air-dry for up to 103 years

Our aim was to compare the soil microbial biomass concentration and its activity (measured as CO₂-C evolved) following the rewetting and aerobic incubation of soils which have previously been stored air-dry for different periods. Some of the soils have been stored in the Rothamsted sample archive for 103 years, others were comparable freshly sampled soils following air-drying and rewetting and other soils were stored air-dry for 2 years then rewetted for the work described here. Following air-drying, soil ATP concentrations were variable in recently air-dried soil, comprising about 10-35% of the initial ATP concentrations in fresh soil. Following rewetting, the percentage recovery of ATP increased in all soils by 7 days, then declined to between 73% and 87% of the original ATP concentration in the air-dried soils by day 12. Storage of air-dried soils decreased the ability of the microbial biomass to restore its ATP concentrations. For example, the ATP concentration in a soil sampled from stubbed (i.e. tree seedling, saplings and bushes cut frequently to ground level) grassland of the Broadbalk continuous wheat experiment at Rothamsted then air-dried for 2 years was only about 14% of that in the fresh soil at 2 days after rewetting. In other soils from the Hoosfield Barley Experiment, also at Rothamsted, previously given NPK or FYM since 1852, and sampled then stored air-dry for between 13 and 83 years, from 52% to 57% of the ATP in the comparable fresh soils was measured at two days after rewetting. The soil ATP concentration then changed little more up to 12 days. One of the most interesting findings was that while the microbial biomass ATP concentration in the above NPK soils only ranged from about 2 to 4 μmol ATP g⁻¹ biomass C, in the FYM soil the microbial biomass ATP concentrations (range 11.5-13.6 μmol ATP g⁻¹ biomass C) were the same as we repeatedly measure in fresh moist aerobic soil. We do not yet know the reasons for this. More than twice as much CO₂-C was evolved from the long-term stored soils than from freshly sampled ones. However, the specific respiration of the microbial biomass did not change much after the first 12 years of storage, indicating that loss of viability mainly occurred in the earlier years.     

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.     

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.     

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.     

Determination of the fate of regularly applied 13C‐labeled‐artificial‐exudates C in two agricultural soils

Exudates are part of the total rhizodeposition released by plant roots to soil and are considered as a substantial input of soil organic matter. Exact quantitative data concerning the contribution of exudates to soil C pools are still missing. This study was conducted to reveal effects of ¹³C‐labeled exudate (artificial mixture) which was regularly applied to upper soil material from two agricultural soils. The contribution of exudate C to water‐extractable organic C (WEOC), microbial biomass C (MBC), and CO₂‐C evolution was investigated during a 74 d incubation. The WEOC, MBC, and CO₂‐C concentrations and the respective δ¹³C values were determined regularly. In both soils, significant incorporation of artificial‐exudate‐derived C was observed in the WEOC and MBC pool and in CO₂‐C. Up to approx. 50% of the exudate‐C amounts added were recovered in the order WEOC << MBC < CO₂‐C in both soils at the end of the incubation. Newly built microbial biomass consisted mainly of exudates, which substituted soil‐derived C. Correspondingly, the CO₂‐C evolved from exudate‐treated soils relative to the controls was dominated by exudate C, showing a preferential mineralization of this substrate. Our results suggest that the remaining 50% of the exudate C added became stabilized in non‐water‐extractable organic fractions. This assumption was supported by the determination of the total organic C in the soils on the second‐last sampling towards the end of the incubation. In the exudate‐treated soils, significantly more soil‐derived C compared to the controls was found in the WEOC on almost all samplings and in the MBC on the first sampling. This material might have derived from exchange processes between the added exudate and the soil matrix. This study showed that easily available substrates can be stabilized in soil at least in the short term.     

Immediate and subsequent effects of drying and rewetting on microbial biomass in a paddy soil

Many surface soils in Japan may experience more frequent and intense drying–rewetting (DRW) events due to future climate changes. Such DRW events negatively and positively affect microbial biomass carbon (MBC) through microbial stress and substrate supply mechanisms, respectively. To assess the MBC immediately after DRW and during the incubation with repeated DRW cycles, two laboratory experiments were conducted for a paddy soil. In the first experiment, we exposed the soil to different drying treatments and examined the MBC and hourly respiration rates immediately after the rewetting to evaluate the microbial stress. In the second experiment, we compared microbial growth rates during the incubation of the partially sterilized soil with a continuously moist condition and repeated DRW cycles to evaluate the contribution of the substrate supply from non-biomass soil organic C on MBC. First, all drying treatments caused a reduction in MBC immediately after the rewetting, and higher drying intensities induced higher reduction rates in MBC. A reduction of more than 20% in MBC induced the C-saturated conditions for surviving microbes because sufficient concentrations of labile substrate C were released from the dead MBC. Second, repeated DRW cycles caused increases in the microbial growth rates because substrate C was supplied from non-biomass organic C. In conclusion, MBC decreased immediately after DRW due to microbial stress, whereas MBC increased during repeated DRW cycles due to substrate C supplied from non-biomass organic C.     

Episodic rewetting enhances carbon and nitrogen release from chaparral soils

The short-term pulse of carbon (C) and nitrogen (N) mineralization that accompanies the wetting of dry soils may dominate annual C and N production in many arid and semi-arid environments characterized by seasonal transitions. We used a laboratory incubation to evaluate the impact of short-term fluctuations in soil moisture on long-term carbon and nitrogen dynamics, and the degree to which rewetting enhances C and N release. Following repeated drying and rewetting of chaparral soils, cumulative CO₂ release in rewet soils was 2.2-3.7 times greater than from soils maintained at equivalent mean soil moisture and represented 12-18% of the total soil C pool. Rewetting frequency did not affect cumulative CO₂ release but did enhance N turnover, and net N mineralization and nitrification increased with rewetting in spite of significant reductions in nitrification potential. Litter addition decreased inorganic N release but enhanced dissolved organic nitrogen (DON) and dissolved organic carbon (DOC) from dry soils, indicating the potential importance of a litter-derived pulse to short-term nutrient dynamics.     

Responses of carbon,nitrogen and phosphorus to two consecutive drying–rewetting cycles in soils

Drying and rewetting cycles are known to be important for the dynamics of carbon (C), phosphorus (P), and nitrogen (N) in soils. This study reports the short‐term responses of these nutrients to consecutive drying and rewetting cycles and how varying soil moisture content affects microbial biomass C and P (MBC and MBP), as well as associated carbon dioxide (CO₂) and nitrous oxide (N₂O) emissions. The soil was incubated for 14 d during which two successive drying–rewetting episodes were imposed on the soils. Soils subjected to drying (DRW) were rewetted on the seventh day of each drying period to return them to 60% water holding capacity, whilst continually moist samples (M), with soil maintained at 60% water holding capacity, were used as control samples. During the first seven days, the DRW samples showed significant increases in extractable ammonium, total oxidized nitrogen, and bicarbonate extractable P concentrations. Rewetting after the first drying event produced significant increases only in CO₂ flux (55.4 µg C g^?1 d^?1). The MBC and MBP concentrations fluctuated throughout the incubation in both treatments and only the second drying–rewetting event resulted in a significantly MBC decrease (416.2 and 366.8 mg kg^?1 in M and DRW soils, respectively). The two drying–rewetting events impacted the microbial biomass, but distinguishing the different impacts of microbial versus physical impacts of the perturbation is difficult. However, this study, having a combined approach (C, N, and P), indicates the importance of understanding how soils will react to changing patterns of drying–rewetting under future climate change.     

Organic carbon mineralization responses to temperature increases in subtropical paddy soils

Purpose

Understanding organic carbon mineralization and its temperature response in subtropical paddy soils is important for the regional carbon balance. There is a growing interest in factors controlling soil organic carbon (SOC) mineralization because of the potential for climate change. This study aims to test the hypothesis that soil clay content impedes SOC mineralization in subtropical paddy soils.

Materials and methods

A 160-day laboratory incubation at temperatures from 10 to 30 °C and 90% water content was conducted to examine the dynamics of SOC mineralization and its temperature response in three subtropical paddy soils with different clay contents (sandy loam, clay loam, and silty clay soils). A three-pool SOC model (active, slow, and resistant) was used to fit SOC mineralization.

Results and discussion

Total CO₂ evolved during incubation following the order of clay loam > silty clay > sandy loam. The temperature response coefficients (Q ₁₀) were 1.92?±?0.39, 2.36?±?0.22, and 2.10?±?0.70, respectively, for the sandy loam soil, clay loam soil, and silty clay soil. But the soil clay content followed the order of silty clay > clay loam > sandy loam. The sandy loam soil neither released larger amounts of CO₂ nor showed higher temperature sensitivity, as expected, even though it contains lower soil clay content among the three soils. It seems that soil clay content did not have a dominant effect which results in the difference in SOC mineralization and its temperature response in the selected three paddy soils. However, dissolved organic carbon (DOC; representing substrate availability) had a great effect. The size of the active C pool ranged from 0.11 to 3.55% of initial SOC, and it increased with increasing temperature. The silty clay soil had the smallest active C pool (1.40%) and the largest Q ₁₀ value (6.33) in the active C pool as compared with the other two soils. The mineralizable SOC protected in the silty clay soil, therefore, had even greater temperature sensitivity than the other two soils that had less SOC stabilization.

Conclusions

Our study suggests that SOC mineralization and its temperature response in subtropical paddy soils were probably not dominantly controlled by soil clay content, but the substrate availability (represented as DOC) and the specific stabilization mechanisms of SOC may have great effects.     

Impact of addition of different rates of rice-residue biochar on C and N dynamics in texturally diverse soils

Impacts of crop residue biochar on soil C and N dynamics have been found to be subtly inconsistent in diverse soils. In the present study, three soils differing in texture (loamy sand, sandy clay loam and clay) were amended with different rates (0%, 0.5%, 1%, 2% and 4%) of rice-residue biochar and incubated at 25°C for 60 days. Soil respiration was measured throughout the incubation period whereas, microbial biomass C (MBC), dissolved organic C (DOC), NH₄⁺-N and NO₃^–N were analysed after 2, 7, 14, 28 and 60 days of incubation. Carbon mineralization differed significantly between the soils with loamy sand evolving the greatest CO₂ followed by sandy clay loam and clay. Likewise, irrespective of the sampling period, MBC, DOC, NH₄⁺-N and NO₃^–N increased significantly with increasing rate of biochar addition, with consistently higher values in loamy sand than the other two soils. Furthermore, regardless of the biochar rates, NO₃^–-N concentration increased significantly with increasing period of incubation, but in contrast, NH₄⁺-N temporarily increased and thereafter, decreased until day 60 in all soils. It is concluded that C and N mineralization in the biochar amended soils varied with the texture and native organic C status of the soils.     

Drivers of microbial respiration and net N mineralization at the continental scale

The dominant pools of C and N in the terrestrial biosphere are in soils, and understanding what factors control the rates at which these pools cycle is essential in understanding soil CO₂ production and N availability. Many previous studies have examined large scale patterns in decomposition of C and N in plant litter and organic soils, but few have done so in mineral soils, and fewer have looked beyond ecosystem specific, regional, or gradient-specific drivers. In this study, we examined the rates of microbial respiration and net N mineralization in 84 distinct mineral soils in static laboratory incubations. We examined patterns in C and N pool sizes, microbial biomass, and process rates by vegetation type (grassland, shrubland, coniferous forest, and deciduous/broadleaf forest). We also modeled microbial respiration and net N mineralization in relation to soil and site characteristics using structural equation modeling to identify potential process drivers across soils. While we did not explicitly investigate the influence of soil organic matter quality, microbial community composition, or clay mineralogy on microbial process rates in this study, our models allow us to put boundaries on the unique explanatory power these characteristics could potentially provide in predicting respiration and net N mineralization. Mean annual temperature and precipitation, soil C concentration, microbial biomass, and clay content predicted 78% of the variance in microbial respiration, with 61% explained by microbial biomass alone. For net N mineralization, only 33% of the variance was explained, with mean annual precipitation, soil C and N concentration, and clay content as the potential drivers. We suggest that the high R² for respiration suggests that soil organic matter quality, microbial community composition, and clay mineralogy explain at most 22% of the variance in respiration, while they could explain up to 67% of the variance in net N mineralization.     

Soil carbon responses to past and future CO2 in three Texas prairie soils

Changes in soil carbon storage could affect and be affected by rising atmospheric CO₂. However, it is unlikely that soils will respond uniformly, as some soils are more sensitive to changes in the amount and chemistry of plant tissue inputs whereas others are less sensitive because of mineralogical, textural, or microbial processes. We studied soil carbon and microbial responses to a preindustrial-to-future CO₂ gradient (250–500 ppm) in a grassland ecosystem in the field. The ecosystem contains three soil types with clay fractions of 15%–55%: a sandy loam Alfisol, a silty clay Mollisol, and a black clay Vertisol. Soil and microbial responses to atmospheric CO₂ are plant-mediated; and aboveground plant productivity in this ecosystem increased linearly with CO₂ in the sandy loam and silty clay. Although total soil organic carbon (SOC) did not change with CO₂ treatment after four growing seasons, fast-cycling SOC pools increased with CO₂ in the two clay soils. Microbial biomass increased 18% and microbial activity increased 30% across the CO₂ gradient in the black clay (55% clay), but neither factor changed with CO₂ in the sandy loam (15% clay). Similarly, size fractionation of SOC showed that coarse POM-C, the youngest and most labile fraction, increased four-fold across the CO₂ gradient in the black clay, but increased by only 50% across the gradient in the sandy loam. Interestingly, mineral-associated C, the oldest and most recalcitrant fraction, declined 23% across the gradient in the third soil type, a silty clay (45% clay). Our results provide evidence for priming in this soil type, as labile C availability and decomposition rate (measured as soil respiration and soil C mineralization) also increased across the CO₂ gradient in the silty clay soil. In summary, CO₂ enrichment in this grassland increased the fast-cycling SOC pool as in other CO₂ studies, but only in the two high-clay soils. Priming in the silty clay could limit SOC accumulation after prolonged CO₂ exposure. Because soil texture varies geographically, including data on soil types could enhance predictions of soil carbon and microbial responses to future CO₂ levels.     

High clay content accelerates the decomposition of fresh organic matter in artificial soils

Clay is generally considered an important stabiliser that reduces the rate of decomposition of organic matter (OM) in soils. However, several recent studies have shown trends contradicting this widely held view, emphasising our poor understanding of the mechanisms underlying the clay effects on OM decomposition. Here, an incubation experiment was conducted using artificial soils differing in clay content (0, 5, and 50%) at different temperatures (5, 15, and 25 °C) to determine the effects of clay content, temperature and their interaction on fresh OM decomposition. CO₂ efflux was measured throughout the experiment. Phospholipid fatty acids (PLFAs), enzyme activities, microbial biomass carbon (MBC), and dissolved organic carbon (DOC) were also measured at the end of the pre-incubation and incubation periods in order to follow changes in microbial community structure, functioning, and substrate availability. The results showed that higher clay contents promoted OM decomposition probably by increasing substrate availability and by sustaining a greater microbial biomass, albeit with a different community structure and with higher activities of most of the extracellular enzymes assayed. Higher clay content induced increases in the PLFA contents of all bacterial functional groups relative to fungal PLFA content. However, clay content did not change the temperature sensitivity (Q₁₀) of OM decomposition. The higher substrate availability in the high clay artificial soils sustained more soil microbial biomass, resulting in a different community structure and different functioning. The higher microbial biomass, as well as the changed community structure and functions, accelerated OM decomposition. From these observations, an alternative pathway to understanding the effects of clay on OM decomposition is proposed, in which clay may not only accelerate the decomposition of organic materials in soils but also facilitate the SOM accumulation as microbial products in the long term. Our results highlight the importance of clay content as a control over OM decomposition and greater attention is required to elucidate the underlying mechanisms.     

Assessment of Methods for Measuring Soil Microbial Biomass Carbon in Temperate Fruit Tree-Based Ecosystems

We investigated the potential of three methods of quantifying microbial biomass carbon (MBC), viz., chloroform fumigation-extraction (CFE) following organic C estimation through Vance method (CFE-V) and Snyder–Trofymow method (CFE-ST), and substrate-induced respiration (SIR) method in soils under various temperate fruit crops along with a control (no plantation) at 0–20 and 21–40 cm soil depths. CFE methods have shown significant (p < 0.05) increase in chloroform labile C in all orchards over the control in surface soil. The interaction between the fruit crops and methods, although significant (p < 0.01), indicated that CFE-ST and SIR methods were statistically at par with each other within the same fruit crop, except peach plantation (CEF-ST significantly lower than SIR) in 0–20 cm soil depth. The coefficient of variation recorded for chloroform labile organic C estimates by CFE-ST method makes it more precise than CFE-V method, especially in 0–20 cm soil depth. The very close agreement between the methods suggests that over this narrower range (i.e., smaller geographical area) all methods are appropriate for assessing MBC. However, SIR, being most sensitive to orchard plantations and strongly correlated with various soil chemical properties, could preferably be recommended for estimation of MBC in such soils. As an alternative to CFE-V method, CFE-ST may also be used for estimation of chloroform labile organic C in these soils.     

Short-term temperature dependence of heterotrophic soil respiration after one-month of pre-incubation at different temperatures

Quantification of microbial activities involved in soil organic carbon (SOC) decomposition is critical for the prediction of the long-term impact of climate change on soil respiration (SR) and SOC stock. Although the temperature sensitivity of SR is especially critical in semi-arid regions, such as North West Tunisia, where the SOC stock is low, little research has been carried out in these environments. More needs to be known about factors, such as SOC availability that influence temperature sensitivity. In this study, soil samples were incubated with and without glucose addition for 28 days after a 28-day pre-incubation period. Pre-incubation and incubation was carried out at 20 °C, 30 °C, 40 °C and 50 °C. Respiration measurements were taken with temperature, glucose addition and incubation time as independent variables. The highest pre-incubation temperature reduced the temperature sensitivity of SR during the subsequent incubation period, both with and without glucose addition. Soil samples pre-incubated at 50 °C had the lowest SR at all subsequent incubation temperatures and the lowest temperature sensitivity of SR, even after glucose addition. However, after glucose addition, the effect of a high pre-incubation temperature on soil respiration lasted only two days. Measuring the water-soluble carbon (WSC) in soil samples suggested that the high pre-incubation temperature may have killed part of the microbial biomass, modified microbial communities or solubilized SOC. For quantifying the possible effect of global warming, in particular heat waves, on soil respiration in the soil studied, the results indicate a moderate response of soil respiration to temperature at high temperatures, as shown by Q₁₀ close to 1.7, even in the range 40-50 °C.     

The proportional mineralisation of microbial biomass and organic matter caused by air-drying and rewetting of a grassland soil

During the first few days after rewetting of an air-dried soil (AD-RW), microbial activity increases compared to that in the original moist soil, causing increased mineralisation (a flush) of soil organic carbon (C) and other nutrients. The AD-RW flush is believed to be derived from the enhanced mineralisation of both non-biomass soil organic matter (due to its physical release and enhanced availability) and microbial biomass killed during drying and rewetting. Our aim was to determine the effects of AD-RW on the mineralisation of soil organic matter and microbial biomass during and after repeated AD-RW cycles and to quantify their proportions in the CO₂-C flushes that resulted. To do this, a UK grassland soil was amended with ¹⁴C-labelled glucose to label the biomass and then given five AD-RW cycles, each followed by 7 d incubation at 25 °C and 50% water holding capacity. Each AD-RW cycle increased the amount of CO₂-C evolved (varying from 83 to 240 μg g⁻¹ soil), compared to the control with, overall, less CO₂-C being evolved as the number of AD-RW cycles increased. In the first cycle, the amount of biomass C decreased by 44% and microbial ATP by 70% while concentrations of extractable C nearly doubled. However, all rapidly recovered and within 1.3 d after rewetting, biomass C was 87% and ATP was 78% of the initial concentrations measured prior to air-drying. Similarly, by 2 d, extractable organic C had decreased to a similar concentration to the original. After the five AD-RW cycles, the amounts of total and ¹⁴C-labelled biomass C remaining in the soil accounted for 60 and 40% of those in the similarly incubated control soil, respectively. Soil biomass ATP concentrations following the first AD-RW cycle remained remarkably constant (ranging from about 10 to 14 μmol ATP g⁻¹ biomass C) and very similar to the concentration in the fresh soil prior to air-drying. We developed a simple mathematical procedure to estimate the proportion of CO₂-C derived from biomass C and non-biomass C during AD-RW. From it, we estimate that, over the five AD-RW cycles, about 60% of the CO₂-C evolved came from mineralisation of non-biomass organic C and the remainder from the biomass C itself.     

CO2 emissions from subtropical arable soils of China

CO₂ efflux plays a key role in carbon exchange between the biosphere and atmosphere, but our understanding of the mechanism controlling its temporal and spatial variations is limited. The purpose of this study is to determine annual soil CO₂ flux and assess its variations in arable subtropical soils of China in relation to soil temperature, moisture, rainfall, microbial biomass carbon (MBC) and dissolved organic carbon (DOC) using the closed chamber method. Soils were derived from three parent materials including granite (G), tertiary red sandstone (T) and quaternary red clay (Q). The experiment was conducted at the Ecological Station of Red Soil, The Chinese Academy of Sciences, in a subtropical region of China. The results showed that soil CO₂ flux had clear seasonal fluctuations with the maximum value in summer, the minimum in winter and intermediate in spring and autumn. Further, significant differences in soil CO₂ flux were found among the three red soils, generally in the order of G>T>Q. The average annual fluxes were estimated as 2.84, 2.13 and 1.41 kg CO₂ m⁻² year⁻¹ for red soils derived from G, T and Q, respectively. Soil temperature strongly affects the seasonal variability of soil CO₂ flux (85.0-88.5% of the variability), followed by DOC (55.8-84.4%) and rainfall (43.0-55.8%). The differences in soil CO₂ flux among the three red soils were partly explained by MBC (33.7-58.9% of the variability) and DOC (23.8-33.6%).     

鄂尔多斯高原脉冲降雨对油蒿灌丛群落土壤碳排放的影响

Precipitation is the major driver of ecosystem functions and processes in semiarid and arid regions. In such water-limited ecosystems, pulsed water inputs directly control the belowground processes through a series of soil drying and rewetting cycles. To investigate the effects of sporadic addition of water on soil CO₂ efflux, an artificial precipitation event (3 mm) was applied to a desert shrub ecosystem in the Mu Us Sand Land of the Ordos Plateau in China. Soil respiration rate increased 2.8-4.1 times immediately after adding water in the field, and then it returned to background level within 48 h. During the experiment, soil CO₂ production was between 2 047.0 and 7 383.0 mg m^-2. In the shrubland, soil respiration responses showed spatial variations, having stronger pulse effects beneath the shrubs than in the interplant spaces. The spatial variation of the soil respiration responses was closely related with the heterogeneity of soil substrate availability. Apart from precipitation, soil organic carbon and total nitrogen pool were also identified as determinants of soil CO₂ loss in desert ecosystems.