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1.
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   

2.
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.  相似文献   

3.
Temperature, drying, and rewetting are important climatic factors that control microbial properties. In the present study we looked at the respiration rates, adenosine 5′‐triphosphate (ATP) content, and adenylate energy charge (AEC) as a measure for energy status of microbial biomass in the upper 5 cm of mineral soils of three beech forests at different temperatures and after rewetting. The soils differed widely in pH (4.0 to 6.0), microbial biomass C (92 to 916 μg (g DW)—1) and ATP content (2.17 to 7.29 nmol ATP (g DW)—1). The soils were incubated for three weeks at 7 °C, 14 °C, and 21 °C. After three weeks the microbial properties were determined, retaining temperature conditions. The temperature treatment did not significantly affect AEC or ATP content, but respiration rates increased significantly with increasing temperature. In a second experiment the soils were dried for 12 hours at 40 °C. Afterwards the soils were rewetted and microbial properties were monitored for 72 hours. After the drying, respiration rates dropped below the detection limit, but within one hour after rewetting respiration rates increased above control level. Drying reduced AEC by 16 % to 44 % and ATP content by 47 % to 78 %, respectively. Rewetting increased AEC and ATP content significantly as compared to dry soil, but after 72 hours the level of the controls was still not reached. The level of AEC values indicated dormant cells, but ATP content increased. These results indicate that the microbial carbon turnover was not directly linked to microbial growth or microbial energy status. Furthermore our results indicate that AEC may describe an average energy status but does not reflect phases of growing, dormant, or dying cells in the complex microbial populations of soils.  相似文献   

4.
An incubation experiment was conducted to determine the response of soil microbial biomass and activity to salinity when supplied with two different carbon forms. One nonsaline and three saline soils of similar texture (sandy clay loam) with electrical conductivities of the saturation extract (ECe) of 1, 11, 24 and 43 dS m?1 were used. Carbon was added at 2.5 and 5 g C kg?1 (2.5C, 5C) as glucose or cellulose; soluble N and P were added to achieve a C/N ratio of 20 and C/P ratio of 200. Soil microbial activity was assessed by measuring CO2 evolution continuously for 3 weeks; microbial biomass C and available N and P were determined on days 2, 7, 14 and 21. In all soils, cumulative respiration was higher with 5C than with 2.5C and higher with glucose than with cellulose. Cumulative respiration was highest in the nonsaline soil and decreased with increasing EC, whereas the decrease was gradual with glucose, there was a sharp drop in cumulative respiration with cellulose from the nonsaline soil to soil with EC11 with little further decrease at higher ECs. Microbial biomass C and available N and P concentrations were highest in the nonsaline soil but did not differ among the saline soils. Microbial biomass C was higher and available N was lower with 5C than with 2.5C. The C form affected the temporal changes of microbial biomass and available nutrients differentially. With glucose, microbial biomass was highest on day 2 and then decreased, whereas available N showed the opposite pattern, being lowest on day 2 and then increasing. With cellulose, microbial biomass C increased gradually over time, and available N decreased gradually. It is concluded that salinity reduced the ability of microbes to decompose cellulose more than that of glucose.  相似文献   

5.
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.  相似文献   

6.
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   

7.
Most important, yet least understood, question, how microbial activity in soil under saline water irrigation responds to carbon (C) varying qualitatively (most labile form to extreme recalcitrant form) with or without maintaining C/N ratio was investigated in an incubation experiment. Soil samples from a long-term saline-water (electrical conductivity, EC ≈ 0, 6, and 12 dS m?1)- irrigated field were incorporated with three different C substrates, viz., glucose, rice straw (RS), and biochar with or without nitrogen (N as ammonium sulfate, NH4SO4) and were incubated at 25 °C for 56 days. Cumulative respiration (CR), microbial biomass carbon (MBC), microbial biomass nitrogen (MBN), and dehydrogenase activity (DEA) concentrations decreased with increasing EC (P < 0.05), but less so in soils amended with glucose followed by RS and biochar. The addition of N to soils amended with different C substrates significantly decreased CR, MBC, DEA, and available phosphorus (P) concentrations at a given EC level.  相似文献   

8.
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   

9.
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   

10.
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   

11.
The effects of adding P and of drying and rewetting were studied in two acid forest soils from southeast Australia. The soils were a yellow podzolic with a low soil organic matter content (3.75% C) and a red earth with a high organic matter content (13.5% C). C and N mineralization and microbial C and N contents were investigated in a laboratory incubation for 151 days. Microbial C and N were estimated by a hexanol fumigation-extraction technique. Microbial C was also determined by substrate-induced respiration combined with a selective inhibition technique to separate the fungal and the bacterial biomass. The results obtained by the selective inhibition technique were not conclusive. Adding P to the soil and drying and rewetting the soil reduced microbial N. This effect was more pronounced in rapidly and frequently dried soils. Microbial C was generally less affected by these treatments. Compared with the control, the addition of P caused a reduction in respiration in the red earth (-13%) but an increase in the yellow podzolic soil (+12%). In the red earth net N mineralization was highest following the addition of P. In the yellow podzolic soil highest N mineralization rates were obtained when the soil was subjected to drying and rewetting cycles. In both soils increased N mineralization was associated with a decrease in microbial N, indicating that the mineralized N was of microbial origin. Nitrification decreased with rapid drying and rewetting. The addition of P promoted heterotrophic nitrification in both soils.  相似文献   

12.
Soil samples of parabrown earth and chernozem, each having a different amount of microbial biomass, were used to investigate the contribution of microbial cells to the pool of mobile plant nutrients in soils. The quantities of nutrients mobilized in soils which had been dried or fumigated were closely related to the quantities available in freshly-killed biomass. For the percent of N mineralized from dead microbial biomass in arable soil during 28 days, a “kN-factor” (28 days) of 0.37 was suggested. In oven-dried (70°C) and air-dried (room temperature) soils, approximately 77 and 55% of the N mineralized after remoistening and incubating at 22°C for 4 weeks came from the freshly-killed biomass. The remaining 23 and 45% were derived from non-biomass organic N fractions of the soils. In fumigation experiments (CHCl3, 24 h), the amount of P released was closely related to the P content of the soil microbial biomass. The fluctuating amounts of K available after fumigation did not correspond to the amount of biomass killed. A scheme for the transformation of dead microbial biomass-C and -N in arable soil is suggested.  相似文献   

13.
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   

14.
The ratios of soil carbon (C) to nitrogen (N) and C to phosphorus (P) are much higher in Chinese temperate forest soils than in other forest soils, implying that N and P might limit microbial growth and activities. The objective of this study was to assess stoichiometric responses of microbial biomass, enzyme activities, and respiration to N and P additions. We conducted a nutrient (N, P, and N + P) addition experiment in two temperate soils under Korean pine (Pinus koraiensis) plantation and natural broadleaf forest in Northeast China and measured the microbial biomass C, N, P; the activities of β-glucosidase (BG), N-acetyl-β-glucosaminidase (NAG), and acid and alkaline phosphomonoesterase (AP); and the microbial respiration in the two soils. Nitrogen addition increased microbial biomass N and decreased microbial biomass C-to-N ratio and microbial respiration in the two soils. Nitrogen addition decreased NAG activity to microbial biomass N ratio, P addition decreased AP activity to microbial biomass P ratio, and N, P, and N + P additions all increased BG activity to microbial biomass C ratio. These results suggest that microbial stoichiometry is not strictly homeostatic in response to nutrient additions, especially for N addition. The responses of enzyme activities to nutrient additions support the resource allocation theory. The N addition induced a decline in microbial respiration, implying that atmospheric N deposition may reduce microbial respiration, and consequently increase soil C sequestration in the temperate region.  相似文献   

15.
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   

16.
Declining rates of soil respiration are reliably observed during long-term laboratory incubations. However, the cause of this decline is uncertain. We explored different controls on soil respiration to elucidate the drivers of respiration rate declines during long-term soil incubations. Following a long-term (707 day) incubation (30 °C) of soils from two sites (a cultivated and a forested plot at Kellogg Biological Station, Hickory Corners, MI, USA), soils were significantly depleted of both soil carbon and microbial biomass. To test the ability of these carbon- and biomass-depleted (“incubation-depleted”) soils to respire labile organic matter, we exposed soils to a second, 42 day incubation (30 °C) with and without an addition of plant residues. We controlled for soil carbon and microbial biomass depletion by incubating field fresh (“fresh”) soils with and without an amendment of wheat and corn residues. Although respiration was consistently higher in the fresh versus incubation-depleted soil (2 and 1.2 times higher in the fresh cultivated and fresh forested soil, respectively), the ability to respire substrate did not differ between the fresh and incubation-depleted soils. Further, at the completion of the 42 day incubation, levels of microbial biomass in the incubation-depleted soils remained unchanged, while levels of microbial biomass in the field-fresh soil declined to levels similar to that of the incubation-depleted soils. Extra-cellular enzyme pools in the incubation-depleted soils were sometimes slightly reduced and did not respond to addition of labile substrate and did not limit soil respiration. Our results support the idea that available soil organic matter, rather than a lack microbial biomass and extracellular enzymes, limits soil respiration over the course of long-term incubations. That decomposition of both wheat and corn straw residues did not change after major changes in the soil biomass during extended incubation supports the omission of biomass values from biogeochemical models.  相似文献   

17.
Little is known about the effects of temperature and drying–rewetting on soil phosphorus (P) fractions and microbial community composition in regard to different fertilizer sources. Soil P dynamics and microbial community properties were evaluated in a soil not fertilized or fertilized with KH2PO4 or swine manure at two temperatures (10 and 25 °C) and two soil water regimes (continuously moist and drying–rewetting cycles) in laboratory microcosm assays. The P source was the dominant factor determining the sizes of labile P fractions and microbial community properties. Manure fertilization increased the content of labile P, microbial biomass, alkaline phosphomonoesterase activity, and fatty acid contents, whereas KH2PO4 fertilization increased the content of labile inorganic P and microbial P. Water regimes, second to fertilization in importance, affected more labile P pools, microbial biomass, alkaline phosphomonoesterase activity, and fatty acid contents than temperature. Drying–rewetting cycles increased labile P pools, decreased microbial biomass and alkaline phosphomonoesterase activity, and shaped the composition of microbial communities towards those with greater percentages of unsaturated fatty acids, particularly at 25 °C in manure-fertilized soils. Microbial C and P dynamics responded differentially to drying–rewetting cycles in manure-fertilized soils but not in KH2PO4-fertilized soils, suggesting their decoupling because of P sources and water regimes. Phosphorus sources, temperature, and water regimes interactively affected the labile organic P pool in the middle of incubation. Overall, P sources and water availability had greater effects on P dynamics and microbial community properties than temperature.  相似文献   

18.
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   

19.
Little is known about the decomposition rates of shoot and root residues of perennial grasses. This knowledge is important to estimate the carbon sequestration potential of the grasses. An incubation experiment was carried out in a sandy clay loam with shoot and root residues of three native perennial grasses (Wallaby grass, Stipa sp. and Kangaroo grass) and the annual grass barley either separately or in mixtures of two residues. Respiration rate was measured over 18 days, and microbial C and available N were measured on days 0 and 18. Decomposition was lower for roots than for shoots and lower for residues of perennial grasses than for barley. Cumulative respiration was positively correlated with water-soluble C in the residues but not with residue C/N. In the mixtures, the measured cumulative respiration was higher than the expected value in five of the nine mixes usually where the differences in cumulative respiration between the individual residues were relatively small. Lower than expected cumulative respiration were found in two of the mixtures in which barley shoots (high cumulative respiration) were mixed with residues with low cumulative respiration. There was a negative correlation between the change in microbial biomass C concentration from day 0 to day 18 and cumulative respiration on day 18. In the amended soils, the available N concentration decreased from day 0 to day 18. It is concluded that the low decomposition rate of perennial grasses residues should favour C sequestration, but that mixing residues of similar decomposition rate may accelerate their decomposition.  相似文献   

20.
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   

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