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1.
In a greenhouse pot study, we examined the availability of N to grain sorghum from organic and inorganic N sources. The treatments were15N-labeled clover residues, wheat residues, and fertilizer placed on a sandy clay loam and loamy sand soil surface for an 8-week period. Soil aggregates formed under each soil texture were measured after 8 weeks for each treatment. Significantly greater 15N was taken up and recovered by grain sorghum in sandy clay loam pots compared with loamy sand pots. Greater 15N recovery was consistently observed with the inorganic source than the organic sources regardless of soil texture or time. Microbial biomass C and N were significantly greater for sandy clay loam soil compared with the loamy sand. Microbial biomass 15N was also significantly greater in the sandy clay loam treatment compared to the loamy sand. The fertilizer treatment initially had the greatest pool of microbial biomass 15N but decreased with time. The crop residue treatments generally had less microbial biomass 15N with time. The crop residues and soil texture had a significant effect on the water-stable aggregates formed after 8 weeks of treatments. Significantly greater water-stable aggregates were formed in the sandy clay loam than the loamy sand. Approximately 20% greater water-stable aggregates were formed under the crop residue treatments compared to the fertilizer only treatment. Soil texture seemed to be one of the most important factors affecting the availability of N from organic or inorganic N sources in these soils.Contribution from the MissouriAgricultural Experiment Station, Journal Series No.12131  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.
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   

4.
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   

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 NO3N 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 NO3N 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.
Salt-affected soils are widespread, particularly in arid climates, but information on nutrient dynamics and carbon dioxide (CO2) efflux from salt-affected soils is scarce. Four laboratory incubation experiments were conducted with three soils. To determine the influence of calcium carbonate (CaCO3) on respiration in saline and non-saline soils, a loamy sand (6.3% clay) was left unamended or amended with NaCl to obtain an electrical conductivity (EC) of 1.0 dS?m?1 in a 1:5 soil/water extract. Powdered CaCO3 at rates of 0%, 0.5%, 1.0%, 2.5%, 5.0% and 10.0% (w/w) and 0.25-2 mm mature wheat residue at 0% and 2% (w/w) were then added. Cumulative CO2-C emission from the salt amended and unamended soils was not affected by CaCO3 addition. To investigate the effect of EC on microbial activity, soil respiration was measured after amending a sandy loam (18.8% clay) and a silt loam (22.5% clay) with varying amount of NaCl to obtain an EC1:5 of 1.0–8.0 dS?m?1 and 2.5 g glucose C?kg?1 soil. Soil respiration was reduced by more than 50% at EC1:5?≥?5.0 dS?m?1. In a further experiment, salinity up to an EC1:5 of 5.0 dS?m?1 was developed in the silt loam with NaCl or CaCl2. No differences in respiration at a given EC were obtained between the two salts, indicating that Na and Ca did not differ in toxicity to microbial activity. The effect of different addition rates (0.25–2.0%) of mature wheat residue on the response of respiration to salinity was investigated by adding NaCl to the silt loam to obtain an EC1:5 of 2.0 and 4.0 dS?m?1. The clearest difference between salinity levels was with 2% residue rate. At a given salinity level, the modelled decomposition constant ‘k’ increased with increasing residue addition rate up to 1% and then remained constant. Particulate organic carbon left after decomposition from the added wheat residues was negatively correlated with cumulative respiration but positively correlated with EC. Inorganic N (NH 4 + -N and NO 3 ? -N) and resin P significantly decreased with increasing salinity. Resin P was significantly decreased by addition of CaCl2 and CaCO3.  相似文献   

7.
Integrating information on nitrogen (N) mineralization potentials into a fertilization plan could lead to improved N use efficiency. A controlled incubation mineralization study examined microbial biomass dynamics and N mineralization rates for two soils receiving 56 and 168 kg N ha?1 in a Panoche clay loam (Typic Haplocambid) and a Wasco sandy loam (Typic Torriorthent), incubated with and without cotton (Gossypium hirsutum L.) residues at 10 and 25°C for 203 days. Microbial biomass activity determined from mineralized carbon dioxide (CO2) was higher in the sandy loam than in clay loam independent of incubation temperature, cotton residue addition and N treatment. In the absence of added cotton residue, N mineralization rates were higher in the sandy loam. Residue additions increased N immobilization in both soils, but were greater in clay loam. Microbial biomass and mineralization were significantly affected by soil type, residue addition and temperature but not by N level.  相似文献   

8.
Biochar amendments to soils may alter soil function and fertility in various ways, including through induced changes in the microbial community. We assessed microbial activity and community composition of two distinct clayey soil types, an Aridisol from Colorado (CO) in the U.S. Central Great Plains, and an Alfisol from Virginia (VA) in the southeastern US following the application of switchgrass (Panicum virgatum) biochar. The switchgrass biochar was applied at four levels, 0%, 2.5%, 5%, and 10%, approximately equivalent to biochar additions of 0, 25, 50, and 100 t ha-1, respectively, to the soils grown with wheat (Triticum aestivum) in an eight-week growth chamber experiment. We measured wheat shoot biomass and nitrogen (N) content and soil nutrient availability and N mineralization rates, and characterized the microbial fatty acid methyl ester (FAME) profiles of the soils. Net N mineralization rates decreased in both soils in proportion to an increase in biochar levels, but the effect was more marked in the VA soil, where net N mineralization decreased from -2.1 to -38.4 mg kg-1. The 10% biochar addition increased soil pH, electrical conductivity, Mehlich- and bicarbonate-extractable phosphorus (P), and extractable potassium (K) in both soil types. The wheat shoot biomass decreased from 17.7 to 9.1 g with incremental additions of biochar in the CO soil, but no difference was noted in plants grown in the VA soil. The FAME recovery assay indicated that the switchgrass biochar addition could introduce artifacts in analysis, so the results needed to be interpreted with caution. Non-corrected total FAME concentrations indicated a decline by 45% and 34% with 10% biochar addition in the CO and VA soils, respectively, though these differences became nonsignificant when the extraction efficiency correction factor was applied. A significant decline in the fungi:bacteria ratio was still evident upon correction in the CO soil with biochar. Switchgrass biochar had the potential to cause short-term negative impacts on plant biomass and alter soil microbial community structure unless measures were taken to add supplemental N and labile carbon (C).  相似文献   

9.
The soil physicochemical characteristics and amounts of microbial biomass C, N, and S in 19 soils (10 grassland, 2 forest, and 7 arable soils) were investigated to clarify the S status in granitic regosols in Japan, in order to determine the relationships between biomass S and other soil characteristics and to estimate approximately the annual Sand N flux through the microbial biomass. Across the sites, the amount of biomass C ranged from 46 to 1,054, biomass N from 6 to 158, and biomass S from 0.81 to 13.44 mg kg-1 soil with mean values of 438.8, 85.8, and 6.15 mg kg-1 soil, respectively. Microbial biomass Nand S accounted for 3.4–7.7% and 1.1–4.0% of soil total Nand S, respectively. The biomass C: N, C : S, and N : S ratios varied considerably across the sites and ranged from 3.0–10.4, 32.5–87.7, and 5.0–18.8, respectively. Microbial biomass S was linearly related to biomass C and biomass N. The regression accounted for 96.6% for biomass C and 92.9% for biomass N of the variance in the data. The amounts of biomass C, N, and S were positively correlated with a number of soil properties, particularly with the contents of organic C, total N, SO4-S, and electrical conductivity and among themselves. The soil properties, in various linear combinations showed a variability of 84–97% in the biomass nutrients. Stepwise multiple regression indicated that biomass C, N, and S were also dependent on SO4-S as a second factor of significance which could limit microbial growth under the conditions prevailing at the study sites. Annual flux of Nand S was estimated through the biomass using the turnover rates of 0.67 for Nand 0.70 for S to be approximately 129 kg Nand 9.7 kg S ha-1 y-l, respectively, and was almost two times higher in grassland than arable soils.  相似文献   

10.
Osmotic potential (OP) of soil solution may be a more appropriate parameter than electrical conductivity (EC) to evaluate the effect of salts on plant growth and soil biomass.However,this has not been examined in detail with respect to microbial activity and dissolved organic matter in soils with different texture.This study evaluated the effect of salinity and sodicity on respiration and dissolved organic matter dynamics in salt-affected soils with different texture.Four non-saline and non-sodic soils differing in texture (S-4,S-13,S-24 and S-40 with 4%,13%,24% and 40% clay,respectively) were leached using combinations of 1 mol L-1 NaC1 and 1 mol L-1 CaC12 stock solutions,resulting in EC (1:5 soil:water ratio) between 0.4 and 5.0 dS m-1 with two levels of sodicity (sodium absorption ratio (SAR) < 3 (non-sodic) and 20 (sodic),1:5 soil:water ratio).Adjusting the water content to levels optimal for microbial activity,which differed among the soils,resulted in four ranges of OP in all the soils:from-0.06 to--0.24 (controls,without salt added),-0.55 to-0.92,-1.25 to-1.62 and-2.77 to-3.00 Mpa.Finely ground mature wheat straw (20 g kg-1) was added to stimulate microbial activity.At a given EC,cumulative soil respiration was lower in the lighter-textured soils (S-4 and S-13) than in the heavier-textured soils (S-24 and S-40).Cumulative soil respiration decreased with decreasing OP to a similar extent in all the soils,with a greater decrease on Day 40 than on Day 10.Cumulative soil respiration was greater at SAR =20 than at SAR < 3 only at the OP levels between-0.62 and-1.62 MPa on Day 40.In all the soils and at both sampling times,concentrations of dissolved organic C and N were higher at the lowest OP levels (from-2.74 to-3.0 MPa) than in the controls (from-0.06 to-0.24 MPa).Thus,OP is a better parameter than EC to evaluate the effect of salinity on dissolved organic matter and microbial activity in different textured soils.  相似文献   

11.
In greenhouse experiments, we examined the N transferred to intercropped corn from 15N-labeled alfalfa shoot residue and intact roots in an undisturbed soil system in response to two different suppression treatments and complete killing of alfalfa. The alfalfa treatments included complete killing (glyphosate only), glyphosate injury + cutting, and cutting only, with alfalfa shoot residue returned to the soil surface in all three treatments. Corn was planted in each pot following application of the treatments. When alfalfa was suppressed by glyphosate injury + cutting, corn had recovered 12% of the alfalfa N by 8 weeks of growth, but with cutting only, N recovery by corn was reduced to 4.0%. The completekill treatment resulted in 8% recovery by corn of alfalfa N. In all treatments, most of the alfalfa-N remained in the soil organic pool. A second experiment tested a cutting only treatment with 15N-labeled alfalfa residue returned to the soil surface. The 15N-labeled alfalfa residue contributed 4.1% of N to corn during the 8-week growth cycle. Twice as much 15N was found in the active microbial biomass pool in the two treatments with live intereropped plants compared to the monoculture treatments with complete killing (non-intercropped) and the control treatment of alfalfa regrowth only. An analysis of the change in the 15N content of the undisturbed alfalfa roots from just before the suppression until 8 weeks later suggested that approximately 80% of the root 15N was lost from the plant suppressed by cutting. This corresponds to 28% of the total N released from the alfalfa. The results suggest that the degree of legume suppression was a key factor in the availability of legume N to the second crop. When the two species were intercropped, more of the N available from legume residues went to plant uptake and microbial biomass and was not stabilized as quickly in the soil organic pool. Appropriate management schemes must be designed to increase N availability to the second crop without yield reduction. These studies suggest severe suppression is necessary; if successful, more of the N can be maintained in active pools.  相似文献   

12.
Changes in 15N abundance and amounts of biologically active soil nitrogen   总被引:1,自引:0,他引:1  
 Estimation of the capacity of soils to supply N for crop growth requires estimates of the complex interactions among organic and inorganic N components as a function of soil properties. Identification and measurement of active soil N forms could help to quantify estimates of N supply to crops. Isotopic dilution during incubation of soils with added 15NH4 + compounds could identify active N components. Dilution of 15N in KCl extracts of mineral and total N, non-exchangeable NH44 +, and N in K2SO4 extracts of fumigated and non-fumigated soil was measured during 7-week incubation. Samples from four soils varying in clay content from 60 to 710 g kg–1 were used. A constant level of 15N enrichment within KCl and K2SO4 extracted components was found at the end of the incubation period. Total N, microbial biomass C and non-exchangeable NH4 + contents of the soils were positively related to the clay contents. The mineralized N was positively related to the silt plus clay contents. The active soil N (ASN) contained 28–36% mineral N, 29–44% microbial biomass N, 0.3–5% non-exchangeable NH4 + with approximately one third of the ASN unidentified. Assuming that absolute amounts of active N are related to N availability, increasing clay content was related to increased N reserve for crop production but a slower turnover. Received: 7 July 1998  相似文献   

13.
In recent years, there has been a growing need to understand how salinity affects microbial communities in agricultural soils. Archaeal and bacterial community diversities and structures were investigated by high-throughput sequencing analysis of their 16S rRNA in two arable soils with low electrical conductivity(EC)(2.3 and 2.6 dS m-1) and a saline soil(EC = 17.6 dS m-1). The dominant bacterial phyla in the soils were Proteobacteria(relative abundance(RA) = 46.2%), followe...  相似文献   

14.
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.  相似文献   

15.
In saline soils under semi-arid climate, low matric and osmotic potential are the main stressors for microbes. But little is known about the impact of water potential (sum of matric and osmotic potential) and substrate composition on microbial activity and biomass in field collected saline soils. Three sandy loam soils with electrical conductivity of the saturated soil extract (ECe) 3.8, 11 and 21 dS m?1 (hereafter referred to EC3.8, EC11 and EC21) were kept at optimal water content for 14 days. After this pre-incubation, the soils were either left at optimal water content or dried to achieve water potentials of ?2.33, ?2.82, ?3.04 and ?4.04 MPa. Then, the soils were amended with 20 g?kg?1 pea or wheat residue to increase nutrient supply. Carbon dioxide emission was measured over 14 days; microbial biomass C was measured at the end of the experiment. Cumulative respiration decreased with decreasing water potential and was significantly (P?<?0.05) lower in soils at water potential ?4 MPa than in soils at optimal water content. The effect of residue type on the response of cumulative respiration was inconsistent; with residue type having no effect in the saline soils (EC11 and EC21) whereas in the non-saline soil (EC3.8), the decrease in respiration with decreasing water potential was less with wheat than with pea residue. At a given water potential, the absolute and relative (in percentage of optimal water content) cumulative respiration was lower in the saline soils than in the non-saline soil. This can be explained by the lower osmotic potential and the smaller microbial biomass in the saline soils. However, even at a similar osmotic potential, cumulative respiration was higher in the non-saline soil. It can be concluded that high salt concentrations in the soil solution strongly reduce microbial activity even if the water content is relatively high. The stronger relative decrease in microbial activity in the saline soils at a given osmotic potential compared to the non-saline soil suggests that the small biomass in saline soils is less able to tolerate low osmotic potential. Hence, drying of soil will have a stronger negative effect on microbial activity in saline than in non-saline soils.  相似文献   

16.
The application of mineral N fertilizers may influence biologically mediated processes that are important in nutrient transformations and availability. This study was conducted to assess the effect of N application on microbial activities in irrigated and non-irrigated winter wheat systems. Carbon decomposition and microbial biomass C in soils with three N application rates (0, 150, and 300 kg N ha–1 as urea) were measured over 40 days in a laboratory incubation experiment. Carbon, N, and P contents in the soil under the irrigated wheat were higher than those in the soil under the non-irrigated wheat. The reverse trend was observed for soil pH and Ca and Mg contents. However, soils from the two systems had similar C/N ratios. Carbon decomposition and microbial biomass C in the soil under the irrigated wheat increased significantly (p <0.05). Increasing rates of N fertilizer resulted in higher C decomposition and microbial biomass C levels in both soil systems. Results indicate that different wheat cropping systems affect soil properties that will then have an impact on C turnover in the soil. Moreover, the irrigated wheat system favors soil conditions required for a faster C turnover. In conclusion, it is likely that due to positive effects on microbial activity, N fertilization will increase nutrient cycling and, subsequently, crop productivity will improve in N-poor soils.  相似文献   

17.
The turnover of native and applied C and N in undisturbed soil samples of different texture but similar mineralogical composition, origin and cropping history was evaluated at −10 kPa water potential. Cores of structurally intact soil with 108, 224 and 337 g clay kg−1 were horizontially sliced and 15N-labelled sheep faeces was placed between the two halves of the intact core. The cores together with unamended treatments were incubated in the dark at 20 °C and the evolution of CO2-C determined continuously for 177 d. Inorganic and microbial biomass N and 15N were determined periodically. Net nitrification was less in soil amended with faeces compared with unamended soil. When adjusted for the NO3-N present in soil before faeces was applied, net nitrification became negative indicating that NO3-N had been immobilized or denitrified. The soil most rich in clay nitrified least N and 15N. The amounts of N retained in the microbial biomass in unamended soils increased with clay content. A maximum of 13% of the faeces 15N was recovered in the microbial biomass in the amended soils. CO2-C evolution increased with clay content in amended and unamended soils. CO2-C evolution from the most sandy soil was reduced due to a low content of potentially mineralizable native soil C whereas the rate constant of C mineralization rate peaked in this soil. When the pool of potentially mineralizable native soil C was assumed proportional to volumetric water content, the three soils contained similar proportions of potentially mineralizable native soil C but the rate constant of C mineralization remained highest in the soil with least clay. Thus although a similar availability of water in the three soils was ensured by their identical matric potential, the actual volume of water seemed to determine the proportion of total C that was potentially mineralizable. The proportion of mineralizable C in the faeces was similar in the three soils (70% of total C), again with a higher rate constant of C mineralization in the soil with least clay. It is hypothesized that the pool of potentially mineralizable C and C rate constants fluctuate with the soil water content.  相似文献   

18.
Currently, straw transformation in saline soil is largely unknown. The effect of soil salinity on wheat straw transformation and the roles of nitrogen (N) and phosphorus (P) were evaluated in a greenhouse experiment. By sodium chloride (NaCl) addition, straw was applied at the rate of 30 g kg?1 in various saline soils (2.0–4.0 g kg?1). N or combined N and P added in straw amended saline soil (3.0 g kg?1). Three replications of each treatment were sampled to determine straw residues at 30, 60, and 90 d. Results showed straw application significantly increased microbial biomass, especially fungal biomass. Soil salinity increased by 1.0 g kg?1, which decreased straw decomposed rate by 6.3 ~ 11.1%. N application significantly increased straw decomposed rate (p < 0.05), and high salinity obviously inhibited the humidification process of straw. We suggested that straw carbon transformation regulation and little straw residue accumulation in saline soil should arouse more attentions in future studies.  相似文献   

19.
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   

20.
A. M. MAHDY 《土壤圈》2011,21(6):773-781
A greenhouse experiment was conducted to test and compare the suitability of saline compost and saline irrigation water for nutrient status amendment of a slightly productive sandy clay loam soil,to study the macronutrient utilization and dry matter production of wheat(Triticum aestivum c.v.Gemmiza 7) grown in a modified soil environment and to determine the effects of compost and saline irrigation water on soil productivity.The sandy clay loam soil was treated with compost of five rates(0,24,36,48,and 60 m 3 ha-1,equivalent to 0,3,4.5,and 6 g kg-1 soil,respectively) and irrigation water of four salinity levels(0.50(tap water),4.9,6.3,and 8.7 dS m-1).The results indicated that at harvest,the electrical conductivity(EC) of the soil was significantly(P < 0.05) changed by the compost application as compared to the control.In general,the soil salinity significantly increased with increasing application rates of compost.Soluble salts,K,Cl,HCO 3,Na,Ca,and Mg,were significantly increased by the compost treatment.Soil sodium adsorption ratio(SAR) was significantly affected by the salinity levels of the irrigation water,and showed a slight response to the compost application.The soil organic carbon content was also significantly(P < 0.05) affected by application of compost,with a maximum value of 31.03 g kg-1 recorded at the compost rate of 60 m 3 ha-1 and the irrigation water salinity level of 8.7 dS m-1 and a minimum value of 12.05 g kg 1 observed in the control.The compost application produced remarkable increases in wheat shoot dry matter production.The maximum dry matter production(75.11 g pot-1) occurred with 60 m 3 ha-1 compost and normal irrigation water,with a minimum of 19.83 g pot-1 with no addition of compost and irrigation water at a salinity level of 8.70 dS m-1.Significant increases in wheat shoot contents of K,N,P,Na,and Cl were observed with addition of compost.The relatively high shoot N values may be attributed to increases in N availability in the tested soil caused by the compost application.Similarly,significant increases in the shoot contents of Na and Cl may be ascribed to the increase in soil soluble K and Cl.The increases in shoot P,N,and K contributed to the growth stimulation since P supplied by the compost was probably responsible in saline and alkaline soils where P solubility was very low.  相似文献   

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