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1.
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.  相似文献   

2.
S. PAL  P. MARSCHNER 《土壤圈》2016,26(5):643-651
Crop yields in sandy soils can be increased by addition of clay-rich soil, but little is known about the effect of clay addition on nutrient availability after addition of plant residues with different C/N ratios. A loamy sandy soil(7% clay) was amended with a clay-rich subsoil(73% clay) at low to high rates to achieve soil mixtures of 12%, 22%, and 30% clay, as compared to a control(sandy soil alone) with no clay addition. The sandy-clay soil mixtures were amended with finely ground plant residues at 10 g kg~(-1): mature wheat(Triticum aestivum L.) straw with a C/N ratio of 68, mature faba bean(Vicia faba L.) straw with a C/N ratio of 39, or their mixtures with different proportions(0%–100%, weight percentage) of each straw. Soil respiration was measured over days 0–45 and microbial biomass C(MBC), available N, and p H on days 0, 15, 30, and 45. Cumulative respiration was not clearly related to the C/N ratio of the residues or their mixtures, but C use efficiency(cumulative respiration per unit of MBC on day 15) was greater with faba bean than with wheat and the differences among the residue mixtures were smaller at the highest clay addition rate. The MBC concentration was lowest in sole wheat and higher in residue mixtures with 50% of wheat and faba bean in the mixture or more faba bean. Soil N availability and soil p H were lower for the soil mixtures of 22% and 30% clay compared to the sandy soil alone. It could be concluded that soil cumulative respiration and MBC concentration were mainly influenced by residue addition, whereas available N and p H were influenced by clay addition to the sandy soil studied.  相似文献   

3.
Drying and rewetting cycles are known to be important for the turnover of carbon (C) in soil, but less is known about the turnover of phosphorus (P) and its relation to C cycling. In this study the effects of repeated drying-rewetting (DRW) cycles on phosphorus (P) and carbon (C) pulses and microbial biomass were investigated. Soil (Chromic Luvisol) was amended with different C substrates (glucose, cellulose, starch; 2.5 g C kg−1) to manipulate the size and community composition of the microbial biomass, thereby altering P mineralisation and immobilisation and the forms and availability of P. Subsequently, soils were either subjected to three DRW cycles (1 week dry/1 week moist) or incubated at constant water content (70% water filled pore space). Rewetting dry soil always produced an immediate pulse in respiration, between 2 and 10 times the basal rates of the moist incubated controls, but respiration pulses decreased with consecutive DRW cycles. DRW increased total CO2 production in glucose and starch amended and non-amended soils, but decreased it in cellulose amended soil. Large differences between the soils persisted when respiration was expressed per unit of microbial biomass. In all soils, a large reduction in microbial biomass (C and P) occurred after the first DRW event, and microbial C and P remained lower than in the moist control. Pulses in extractable organic C (EOC) after rewetting were related to changes in microbial C only during the first DRW cycle; EOC concentrations were similar in all soils despite large differences in microbial C and respiration rates. Up to 7 mg kg−1 of resin extractable P (Presin) was released after rewetting, representing a 35-40% increase in P availability. However, the pulse in Presin had disappeared after 7 d of moist incubation. Unlike respiration and reductions in microbial P due to DRW, pulses in Presin increased during subsequent DRW cycles, indicating that the source of the P pulse was probably not the microbial biomass. Microbial community composition as indicated by fatty acid methyl ester (FAME) analysis showed that in amended soils, DRW resulted in a reduction in fungi and an increase in Gram-positive bacteria. In contrast, the microbial community in the non-amended soil was not altered by DRW. The non-selective reduction in the microbial community in the non-amended soil suggests that indigenous microbial communities may be more resilient to DRW. In conclusion, DRW cycles result in C and P pulses and alter the microbial community composition. Carbon pulses but not phosphorus pulses are related to changes in microbial biomass. The transient pulses in available P could be important for P availability in soils under Mediterranean climates.  相似文献   

4.
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.  相似文献   

5.
Drying and rewetting are common events in soils during summer, particularly in Mediterranean climate where soil microbes may be further challenged by salinity. Previous studies in non-saline soils have shown that rewetting induces a flush of soil respiration, but little is known about how the extent of drying affects the size of the respiration flush or how drying and rewetting affects soil respiration in saline soils. Five sandy loam soils, ranging in electrical conductivity of the saturated soil extract (ECe) from 2 to 48 dS m−1 (EC2, EC9, EC19, EC33 and EC48), were kept at soil water content optimal for respiration or dried for 1, 2, 3, 4 or 5 days (referred to 1D, 2D, 3D, 4D and 5D) and maintained at the achieved water content for 4 days. Then the soils were rewet to optimal water content and incubated moist for 5 days. Water potential decreased with increasing drying time; in the 5D treatment, the water potential ranged between −15 and −30 MPa, with the lowest potentials in soil EC33. In moist and dry conditions, respiration rates per unit soil organic C (SOC) were highest in soil EC19. Respiration rates decreased with increasing time of drying; when expressed relative to constantly moist soil, the decline was similar in all soils. Rewetting of soils only induced a flush of respiration compared to constantly moist soil when the soils were dried for 3 or more days. The flush in respiration was greatest in 5D and smallest in 3D, and greater in EC2 than in the saline soils. Cumulative respiration per unit SOC was highest in soil EC19 and lowest in soil EC2 Cumulative respiration decreased with increasing time of drying, but in a given soil, the relationship between water potential during the dry phase and cumulative respiration at the end of the experiment was weaker than that between respiration rate during drying and water potential. In conclusion, rewetting induced a flush in respiration only if the water potential of the soils was previously decreased at least 3-fold compared to the constantly moist soil. Hence, only marked increases in water potential induce a flush in respiration upon rewetting. The smaller flush in respiration upon rewetting of saline soils suggests that these soils may be less prone to lose C when exposed to drying and rewetting compared to non-saline soils.  相似文献   

6.
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.  相似文献   

7.
Addition of clay-rich subsoil to sandy soil results in heterogeneous soil with clay peds(2-mm) or finely ground( 2 mm) clay soil(FG), which may affect the nutrient availability. The aim of this study was to assess the effect of clay soil particle size(FG or peds)and properties on nutrient availability and organic C binding in sandy soil after addition of residues with low(young kikuyu grass,KG) or high(faba bean, FB) C/N ratio. Two clay soils with high and low smectite percentage, clay and exchangeable Fe and Al were added to a sandy soil at a rate of 20%(weight/weight) either as FG or peds. Over 45 d, available N and P as well as microbial biomass N and P concentrations and cumulative respiration were greater in soils with residues of KG than FB. For soils with KG residues,clay addition increased available N and initial microbial biomass C and N concentrations, but decreased cumulative respiration and P availability compared to sandy soil without clay. Differences in measured parameters between clay type and size were inconsistent and varied with time except the increase in total organic C in the 53 μm fraction during the experiment, which was greater for soils with FG than with peds. We concluded that the high exchangeable Fe and Al concentrations in the low-smectite clay soil can compensate a lower clay concentration and proportion of smectite with respect to binding of organic matter and nutrients.  相似文献   

8.
On sunny summer days, the top 10 cm of soil in southern Australia are heated to temperatures between 50 and 80 °C for a few hours a day, often for several successive days. These extreme temperature events are likely to have profound effects on the microbiota in these soils, but we do not know how this recurrent heat exposure influences microbial dynamics and associated nutrient cycling. In this study, an air-dry soil from southern Australia was exposed to one or two diurnal heating events with maximum temperature of 50 or 70 °C. The control was left at ambient temperature (Amb). All soils were rapidly rewet. Soil respiration was measured for 7 days after rewetting; microbial biomass C, available N and P were determined before rewetting and 1 and 7 days after rewetting. After heating and before rewetting compared to Amb, microbial biomass C (MBC) was 50–80% lower, but available P was 25% higher in heated soils. Available N differed little between Amb and heated soils. Rewetting resulted in a flush of respiration in Amb and soils heated once, but there was no respiration flush in soils heated twice. Cumulative respiration compared to Amb was about 10% higher in soils heated once and about 25% lower in soils heated twice. In Amb, MBC 1 day after rewetting was similar as before rewetting. But in heated soils, MBC increased from before rewetting to 1 day after rewetting about fourfold. Compared to Amb, available N 1 day after rewetting was 20–30% higher in soils heated to 70 °C. Seven days after rewetting, available N was 10% higher than Amb only in soils heated twice to 70 °C. It can be concluded that diurnal heating kills a large proportion of the microbial biomass and influences soil respiration and nutrient availability after rewetting of soils. The effect of heating depends on both maximum temperature and number of events.  相似文献   

9.
Rewetting a dry soil has long been known to cause a burst of respiration (the “Birch Effect”). Hypothesized mechanisms for this involve: (1) release of cellular materials as a result of the rapid increase in water potential stress and (2) stimulating C-supply to microbes via physical processes. The balance of these factors is still not well understood, particularly in the contexts of multiple dry/wet cycles and of how resource and stress patterns vary through the soil profile. We evaluated the effects of multiple dry/wet cycles on surface and subsurface soils from a California annual grassland. Treatments included 4, 6, and 12 cycles that varied the length of the drying period between rewetting events. Respiration was monitored after each wetting event while extractable C and N, microbial biomass, and microbial activity were assayed initially, after the first rewetting event, and at the end of the experiment. Initially, microbial biomass and activity (respiration, dehydrogenase, and N mineralization) in subsurface soils were ca. 10% and 20% of surface soil levels. After multiple cycles, however, subsurface soil microbial biomass and activity were enhanced by up to 8-fold, even in comparison to the constantly moist treatment. By comparison, surface soil microbial biomass and activity were either moderately (i.e. 1.5 times increase) or not affected by wetting and drying. Drying and rewetting led to a cascade of responses (soluble C release, biomass growth, and enhanced activity) that mobilized and metabolized otherwise unavailable soil carbon, particularly in subsurface soils.  相似文献   

10.
Microbial adaptation to salinity can be achieved through synthesis of organic osmolytes,which requires high amounts of energy;however,a single addition of plant residues can only temporarily improve energy supply to soil microbes.Therefore,a laboratory incubation experiment was conducted to evaluate the responses of soil microbes to increasing salinity with repeated additions of plant residues using a loamy sand soil with an electrical conductivity in saturated paste extract（ECe） of 0.6 dS m-1.The soil was kept non-saline or salinized by adding different amounts of NaCl to achieve ECe of 12.5,25.0 and 50.0 dS m-1.The non-saline soil and the saline soils were amended with finely ground pea residues at two rates equivalent to 3.9 and 7.8 g C kg-1 soil on days 0,15 and29.The soils receiving no residues were included as a control.Cumulative respiration per g C added over 2 weeks after each residue addition was always greater at 3.9 than 7.8 g C kg-1 soil and higher in the non-saline soil than in the saline soils.In the saline soils,the cumulative respiration per g C added was higher after the second and third additions than after the first addition except with3.9 g C kg-1 at ECe of 50 dS m1.Though with the same amount of C added(7.8 g C kg-1),salinity reduced soil respiration to a lesser extent when 3.9 g C kg-1 was added twice compared to a single addition of 7.8 g C kg-1.After the third residue addition,the microbial biomass C concentration was significantly lower in the soils with ECe of 25 and 50 dS m1 than in the non-saline soil at3.9 g C kg-1,but only in the soil with ECe of 50 dS m-1 at 7.8 g C kg-1.We concluded that repeated residue additions increased the adaptation of soil microbial community to salinity,which was likely due to high C availability providing microbes with the energy needed for synthesis of organic osmolytes.  相似文献   

11.
The effects of repeated drying-rewetting (DRW) cycles on the microbial biomass and activity in soils taken from long-term field experiment plots with different fertilization (FERT) management practice histories were studied. We investigated the hypothesis that soil response to DRW cycles differs with soil fertility gradient modified by FERT management practices. The soils were incubated for 51 days, after exposure to either nine or three DRW cycles, or remaining at constant moisture content (CMC) at field capacity. We found that both DRW and FERT significantly affected soil properties including NH4-N, NO3-N, dissolved organic C (DOC), microbial biomass C (Cmic), basal soil respiration rate (BSR), urease activity (URE) and dehydrogenase activity (DHD). Except for NH4-N and BSR, variation in the properties was largely explained by FERT, followed by DRW, and then their interaction. Irrespective of the soils' FERT treatment, repeated DRW cycles significantly raised the DOC and Cmic levels compared with CMC, and the DRW cycles also resulted in a significant decline in BSR and URE and increase in DHD, probably because the organisms were better-adapted to the drying and rewetting stresses. The variations in soil biological properties caused by DRW cycles showed a significantly negative relationship with the soil organic C content measured prior to the start of the DRW experiments, suggesting that soils with higher fertility are better able to maintain their original biological functions (i.e., have a higher functional stability) in response to DRW cycles.  相似文献   

12.
Little is known about the effect of drying and rewetting (DRW) on phosphorus (P) pools in the detritusphere, the soil adjacent to plant residues. Two plant residues differing in their potential to release P during decomposition were used: mature barley straw, C/P 255 or young faba bean, C/P 38. Residues were placed between two PVC caps filled with soil at 50% water-holding capacity with open ends covered by fine mesh onto which the residues were placed. The open ends of the two PVC caps were pressed together with residues in between. For the unamended controls, no residues were placed between the meshes. After 2 weeks incubation, the soil was separated from the residues and then either dried and kept dry for 2 weeks followed by rapid rewetting to 50% water-holding capacity (WHC) rewetting (RW) or maintained at 50% of WHC constantly moist (CM). Bioavailable P pools (readily available P pools: CaCl2- and anion exchange-P; P bound to soil particles: citrate- and HCl-P; acid phosphomonoesterase- and microbial-P) were measured in dry soil and 1, 7, and 14 days after rewetting. Rewetting of dry soils induced a respiration flush on the first day after which respiration rates declined to those in CM. Compared to the unamended soil, the flush was about 75% higher with barley and more than twofold higher with faba bean. P pools were 3–20-fold higher with faba bean than with barley or in the control. At the end of the dry period, most P pools were higher in dry soil compared to CM. Rewetting had little effect on P pools 1, 7, and 14 days after rewetting compared to CM. To investigate if rewetting induced a short pulse of available P, a second experiment was carried out. As in the first experiment, faba bean detritusphere soil and control were generated and then dried or kept at 50% WHC for 2 weeks. Before rewetting, anion exchange membranes (AEM) were placed in the soil which were removed one, 2 or 4 days after rewetting. The P concentration on the AEM was more than threefold higher with faba bean than the control. One day after rewetting, the P concentration on the AEM with faba bean was about threefold higher in RW than in CM, but did not differ between RW and CM in the control. Four days after rewetting, nearly all P pools with faba bean were 10–30% lower in RW than in CM, except citrate-P which was about 5% higher in RW. We conclude that rewetting induces a short pulse of available P if the P pool concentration is high as in the detritusphere of faba bean. If P is removed from the soil (by binding to AEM or uptake by plants), rewetting can induce depletion of P pools compared to CM.  相似文献   

13.
The objective of this study was to determine the total organic carbon (TOC), basal respiration (BR), microbial biomass carbon (MBC), the metabolic quotient (qCO2), and ratio of microbial biomass carbon to total organic carbon (MBC/TOC) at different soil depths in three agroecosystems in Fundo Zamorano Independencia, Cojedes State, Venezuela. The types of agroecosystems studied were short-cycle corn and bean cropland, pastureland, and gallery forest, which was used as the control soil. The BR was determined by measuring the carbon dioxide released in a closed system, and the MBC was analyzed by applying the substrate-induced respiration method. The BR and the MBC varied depending on depth and transect position, decreasing between 18% and 38% at a depth of >10 cm with respect to the measurements taken between 0 and 10 cm. Significantly greater BR and MBC values were found at the middle transect position, where the soils with the greatest moisture content are located. No significant differences for BR, MBC, and qCO2 values were found among the agroecosystems. This was due to the high spatial variability of the physical and chemical properties of the soils in the study site. However, with the application of the Kruskal–Wallis test, significant differences for the TOC and MBC/TOC values were found among the agroecosystems. These results highlight the importance of the type of plant cover over soil in different agroecosystems, mainly on pastureland, which maintains the potential of the inocular mycorrhizal of the soil.  相似文献   

14.
It is well known that calcium (Ca2+) plays an important role in binding organic matter to clay. However, most previous studies were conducted with either topsoil or pure aluminosilicates. Less is known about the effect of Ca2+ on binding of organic matter to clay-rich subsoils, which have lower organic-matter contents than topsoils, and their clays are more strongly weathered than pure aluminosilicates. Two experiments were conducted with a Vertisol subsoil (69% clay): a laboratory incubation and a batch sorption. The mineral substrate in the incubation experiment was pure sand alone or sand amended with 300 g clay kg?1. Powdered calcium sulfate (CaSO4) at rates of 0, 5, 10, and 15 g Ca kg?1 and mature wheat residue at a rate of 20 g kg?1 were added to this mineral substrate and the water content was adjusted to 70% of water-holding capacity. Carbon dioxide release was measured for 28 days. Cumulative respiration per g soil organic carbon (C) (SOC from clay and residues) was increased by clay addition. Increasing Ca2+ addition rate decreased cumulative respiration in the sand with clay but had no effect on respiration in the pure sand. Clay and Ca2+ addition had no significant effect on microbial biomass carbon (MBC) per g SOC but clay addition reduced the concentration of potassium sulfate (K2SO4)–extractable C per g SOC. For the batch sorption experiment, the subsoil was mixed with 0 to 15 g Ca kg?1 and water-extractable organic C (WEOC) derived from mature wheat straw was added at 0, 1485, 3267, and 5099 mg WEOC kg?1. Increasing Ca2+ addition rate increased sorption of WEOC, particularly at the greatest concentration of WEOC added, and decreased desorption. This study confirmed the importance of Ca2+ in binding organic matter to clay and suggests that Ca2+ addition to clay-rich subsoils could be used to increase their organic C sequestration.  相似文献   

15.
Soil microbial activity is greatly affected by soil water content. Determining the appropriate moisture content to rewet soils that have been dried in preparation for laboratory incubations to determine microbial activity can be laborious and time-consuming. The most common methods used achieve sufficient moisture content for peak microbial respiration are gravimetric water content, soil matric potential, or percentage of water-filled pore space (WFPS). Alternatively, a fast, simple, and accurate way to ensure that a given soil receives the appropriate amount of water for peak soil microbial respiration is to rely on natural capillary action for rewetting the dry soil. The capillary method is related to the gravimetric method for water uptake and has a strong correlation with WFPS. A microbial respiration test was conducted to compare rewetting methods. The 24-h carbon dioxide (CO2) / carbon (C) results were very similar and strongly correlated using the gravimetric method and the capillary method for rewetting dried soil.  相似文献   

16.
Drying–rewetting (DRW) cycles are important for soil organic matter turnover; however, few studies have considered the short-term effects on nutrient availability. The pulses in soil respiration, extractable C, P and N pools were quantified after a single DRW cycle (ten sampling times over 49 h). Soil was pre-incubated with or without glucose (2.5 g kg−1) for 10 days to induce differences in the size and activity of the microflora and then either subjected to a single DRW cycle (7-day drying period) or kept constantly moist. A resin extractable P (Presin) method was used and compared to extraction of dissolved organic (DOP) and inorganic P (DIP) with a salt solution. The pulse in soil respiration, extractable organic C (EOC), Presin, DOP and DIP was immediate and greatest in the first 2 h. The Presin pulse was two to three times that measured by solution extraction (DIP). Also, Presin quantified temporal changes in P not apparent in DIP, indicating the advantage of anion-exchange membranes in quantifying short-term changes in P availability. The Presin pulse was smaller in the soil incubated with glucose showing that P pulses will be quantitatively smaller in a soil with an active microbial biomass. In contrast to P, pre-incubation with glucose did not alter EOC concentration or the pulse in EOC after rewetting. The Presin pulse had disappeared by 49 h after DRW despite continued elevated rates of respiration. The sustained increase in DIP following DRW may have implications for plant availability or environmental losses.  相似文献   

17.
An incubation study determined the effect of one dry–rewetting (DRW) event on the turnover of carbon (C), phosphorus (P) and nitrogen (N). Thirty-two soils were collected from different climatic regions of southern Australia, varying in soil type, land use and agronomic management history. We hypothesised that respiration and nutrient pulses are related to soil physio-chemical properties. Respiration (CO2 release) was measured intensively for 90 h after rewetting. C mineralisation (C min) model fitting was used to describe the amount of mineralisable C (Co90 h) and the proportional mineralisation rate (k). Compared to constantly moist soils, 13 soils showed increases in both Co90 h and k, indicating that DRW increased the amount of mineralisable C and the rate at which C was mineralised over the 90-h period. In 17 soils, k was increased but not Co90 h, showing an increase in C mineralisation rate but no change in the amount of mineralisable C. Two soils showed a reduction in k with no change in Co90 h, possibly due to low C contents and small microbial biomass. Only one soil exhibited no change in either Co90 h or k. Multiple linear regression analysis indicated that the magnitude of the increase in mineralisable C in response to the DRW event (∆Co90 h = Co90 h DRW − Co90 h moist) was primarily explained by clay content (39%); however, inclusion of nine soil physio-chemical properties explained more of the variation in ∆Co90 h than any of the properties alone. Five of the nine physio-chemical variables present in the multiple-regression model were related to C content or composition. Pulses in available N and P were not related to ∆Co90 h.  相似文献   

18.
In this study, the effect of drying and rewetting on native P transformations in two red brown soils with different management history was investigated. Three treatments, T1 (constantly moist), T2 (dried for 4 days and then kept dry), T3 (rewetted after 4 days drying) were used. Drying and rewetting caused a rapid increase in microbial P (Pm) and labile organic P (labile Po) within 1 day and a gradual increase in available inorganic P (Colwell). These increases were only temporarily, as Pm and labile Po decreased with time and were at the same level as in the constantly moist soil by the end of the incubation period of 21 days. The effect of drying and rewetting on P transformations strongly depended on soil organic matter content, being more pronounced in the soil with high organic matter content, compared to the soil with low soil organic matter content.  相似文献   

19.
Microbial activity and nutrient release are known to be influenced by organic matter properties,but it is difficult to separate the effect of C/N ratio from that of C/P ratio because in most plant residues both ratios are either high or low.An incubation experimeut was conducted to investigate the effects of reducing the C/N and C/P ratios of slowly decomposable plant residues (young eucalyptus leaves,mature wheat straw,and sawdust) to those of rapidly decomposable residues (young kikuyu shoots) on soil respiration,microbial biomass,and N and P availability.The C/N and C/P ratios of the former were adjusted to 15 and 89,respectively,by adding N as (NH4)2SO4,P as KH2PO4 or both and residues were added at 10 g C kg-1 to a silt loam.Soil respiration was measured over 21 d;microbial biomass C (MBC) and available N and P were measured on days 0,7,and 21.Compared to the unamended soil,addition of kikuyu increased cumulative respiration 20-fold,MBC concentration 4 to 8-fold,and available P concentration up to 4-fold,whereas the increase in available N concentration was small and transient.Cumulative respiration and MBC concentration were low in the sawdust-amended soil and were not influenced by reducing the C/N and C/P ratios.Cumulative respiration with original wheat and eucalyptus was 30％-40％ of that with kikuyu.Reducing the C/N ratio alone or both C/N and C/P ratios increased cumulative respiration and MBC concentration 2-fold compared to the original wheat and eucalyptus,whereas reducing the C/P ratio had little effect.Throughout the experiment,the available N concentration after addition of residues with reduced C/N ratio increased in the following order of eucalyptus ＜ wheat ＜ sawdust.By independently lowering the C/N and C/P ratios,microbial activity was more limited by C and N than P.However,lowering the C/N ratio of very slowly decomposable sawdust had no effect on soil respiration and MBC concentration,suggesting that other properties such as concentration of poorly decomposable C compounds limited decomposition.  相似文献   

20.
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.  相似文献   

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