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1.
《Applied soil ecology》2011,47(3):413-421
Substrate input as well as climatic factors affect C and N cycling and microbial properties in forest soils. We used a microcosm approach to investigate the response of CO2 efflux, net N mineralization, and microbial community-level physiological profile (CLPP) to temperature (5 vs. 15 °C) and substrate (with and without sucrose addition) addition in surface mineral soils collected from 4-, 6-, 13-, and 15-year old (ages in 2007) hybrid poplar (Populus deltoides × Populus × petrowskyana var. Walker) stands in northern Alberta. In the early stage of incubation (0–2 h), CO2 efflux was higher at 5 °C than at 15 °C with little effect from substrate addition, while 24 h after the addition of substrate, CO2 efflux became higher under the 15 °C incubation. After 72 h incubation, temperature and substrate addition effects on CO2 efflux subsided and CO2 efflux rates tended to converge among the treatments. Net N mineralization was significantly affected by substrate addition and stand age, while rates of net ammonification were higher at 5 °C than at 15 °C. Net N mineralization occurred without sucrose addition while net immobilization occurred with sucrose addition. The soil from the youngest stand had the lowest N mineralization rate among the stands for each corresponding substrate-incubation temperature treatment. We used Ecoplates from Biolog™ to study sole-carbon-source-utilization profiles of microbial communities at the end of the incubation. Principal component analysis of C utilization data separated microbial communities with respect to substrate addition, incubation temperature and stand age. Our data showed that organic matter mineralization and microbial substrate utilization were affected by incubation temperature, substrate availability and stand age, indicating that the responses of microbial communities in the studied hybrid poplar plantations to temperature changes were strongly mediated by labile C availability and stand development.  相似文献   

2.
The herbicide sulfentrazone is classified as highly mobile and persistent and this study aimed to examine degradation of this compound on a Typic Hapludox soil that is representative of regions where sulfentrazone is used in Brazil. Soil samples were supplemented with sulfentrazone (0.7 μg active ingredient (a.i.) g?1 soil), and maintained at 27 °C. Soil moisture was corrected to 30%, 70%, or 100% water-holding capacity (WHC) and maintained constant until the end of the experimental period. Soils without added herbicide were used as controls. Aliquots were taken after 14, 30, 60, 120, 180, and 255 days of incubation for quantitative analysis of sulfentrazone residues by gas chromatography. Another experiment was conducted in soil samples, with and without the herbicide, at different temperatures (15, 30, and 40 °C), with moisture kept constant at 70% of WHC. The sulfentrazone residues were quantified by gas chromatography after 14, 30, 60, and 120 days of incubation. Sulfentrazone degradation was not affected by soil moisture. A significant effect was observed for the temperature factor after 120 days on herbicide degradation, which was higher at 30 °C. A half-life of 146.5 days was recorded. It was observed that the herbicide stimulated growth of actinomycetes, whereas bacterial and fungal growth was not affected. The microorganisms selected as potential sulfentrazone degraders were Rhizobium radiobacter, Ralstonia pickettii, Methylobacterium radiotolerans, Cladosporium sp., Eupenicillium sp., and Paecilomyces sp.  相似文献   

3.
《Soil biology & biochemistry》2005,37(8):1411-1418
Recent research has established that microbial processes in the arctic continue even when soils are frozen, and that cold-season processes can be important in the overall annual carbon and nitrogen cycles. Despite the importance of wintertime soil microbial processes, our understanding of their controls remains extremely poor. We particularly have a poor understanding of how microbial substrate use patterns change as soils freeze: do microbes use the same substrates as during the growing season, only slower, or do they switch to using different substrates? We used a 14C isotope equilibration technique to partition respiration between the actively turning over microbial biomass and products pool and the plant detritus pool in a range of Arctic tundra soils. Microbes showed a step-function shift in their metabolism as soils cool from +2 to +0.5 °C, roughly doubling the contribution of recycling of microbial C to total soil respiration. There was no additional shift in substrate use as soils underwent bulk soil freezing. The above-0 °C substrate shift is important because tundra soils spend a long time at or just below 0 °C as they are freezing in the early winter. The change in substrate use represents a shift from processing N-poor detritus to N-rich microbial products, causing N available for either plant uptake or leaching to be greatest when soils are near 0 °C. This may explain the observed patterns of growing season N immobilization vs. cold-season mineralization that appear common in Arctic tundra ecosystems.  相似文献   

4.
The use of organic residues as soil amendments or fertilisers may represent a valuable recycling strategy. In this study, a series of laboratory assays was performed to study the effects of the application of organic residues on C and N mineralization and biochemical properties in a Mediterranean agricultural soil. Two crop residues (straw and cotton) and two animal by-products (meat bone meal and blood meal) were added at three rates (5, 10 and 20 mg g?1 on dry weight basis) to a moist (40% water holding capacity) sandy soil and incubated at 20 °C for 28 days. Each residue underwent a different mineralization pattern depending on the nature and complexity of its chemical constituents. In all cases, the addition of the waste produced, after a short lag-phase, an exponential increase in the soil respiration rate, reflecting the growth of microbial biomass. The amount of total extra CO2-C evolved after 28 days, expressed as % in respect to added C, differed significantly (P < 0.005) among application doses: 5 > 10 > 20 mg g?1 and residue type: meat bone meal > blood meal > cotton cardings > wheat straw. Plant residues led to a rapid immobilisation of N that affected microbial size and activity and further mineralization. Animal by-products produced an immediate and remarkable increase of mineral N in the soil. However, the large amounts of NH4+ released in the soil at high rates of animal residues led, in some cases, to temporary adverse effects on microbial biomass growth and nitrification. All residues produced a significant increase in soil microbial biomass size and activity, being the intensity of the response related to their chemical properties.  相似文献   

5.
With the advent of glyphosate [N-(phosphonomethyl)glycine] tolerant crops, soils have now been receiving repeated applications of the herbicide for over 10 years in the Midwestern USA. There is evidence that long-term use of glyphosate can cause micronutrient deficiency but little is known about plant potassium (K) uptake interactions with glyphosate. The repeated use of glyphosate may create a selection pressure in soil microbial communities that could affect soil K dynamics and ultimately K availability for crops. Therefore, the objectives of this study were to characterize the effect of foliar glyphosate applied to GR (glyphosate resistant) soybeans on: (1) rhizosphere microbial community profiles using ester linked fatty acid methyl ester (EL-FAME) biomarkers, (2) exchangeable, non-exchangeable, and microbial K in the rhizosphere soil, and (3) concentrations of soybean leaf K. A greenhouse study was conducted in a 2 × 2 × 3 factorial design with two soil treatments (with or without long-term field applications of glyphosate), two plant treatments (presence and absence of soybean plants), and three rates of glyphosate treatments (0×, 1× at 0.87, and 2× at 1.74 kg ae ha?1, the recommended field rate). After each glyphosate application, rhizosphere soils were sampled and analyzed for microbial community structure using ester linked fatty acid methyl ester biomarkers (EL-FAME), and exchangeable, plant tissue and microbial biomass K. Glyphosate application caused a significant decrease in the total microbial biomass in soybean rhizosphere soil that had no previous exposure to glyphosate, at 7 days after glyphosate application. However, no significant changes were observed in the overall microbial community structure. In conclusion, the glyphosate application lowered the total microbial biomass in the GR soybean rhizosphere soil that had no previous exposure to glyphosate, at 7 days after glyphosate application; caused no changes in the microbial community structure; and did not reduce the plant available K (soil exchangeable or plant tissue K).  相似文献   

6.
Napropamide is one of the most commonly used herbicide in agricultural practice and can exhibit toxic effect to soil microorganisms. Therefore, the main objective of this study was to examine the genetic and functional diversity of microbial communities in soil treated with napropamide at field rate (FR, 2.25 mg kg−1 of soil) and 10 times the FR (10 × FR, 22.5 mg kg−1 of soil) by the denaturing gradient gel electrophoresis (DGGE) and the community level physiological profile (CLPP) methods. In addition, the r/K-strategy approach was used to evaluate the effect of this herbicide on the community structure of the culturable soil bacteria. DGGE patterns revealed that napropamide affected the structure of microbial community; however, the richness (S) and genetic diversity (H) values indicated that the FR dosage of napropamide experienced non-significant changes. In turn, the 10 × FR dosage of herbicide caused significant changes in the S and H values of dominant soil bacteria. DGGE profiles suggest an evolution of bacteria capable of degrading napropamide among indigenous microflora. Analysis of the CLPPs indicated that the catabolic activity of microbial community expressed as AWCD (average well-color development) was temporary positively affected after napropamide application and resulted in an increase of the substrate richness (SR) as well as functional biodiversity (H) values. Analysis of the bacterial growth strategy revealed that napropamide affected the r- or K-type bacterial classes (ecotypes). In treated-soil samples K-strategists dominated the population, as indicated by the decreased ecophysiological (EP) index. Napropamide significantly affected the physiological state of culturable bacteria and caused a reduction in the rate of colony formation as well as a prolonged time of growth rate. Obtained results indicate that application of napropamide may poses a potential risk for soil functioning.  相似文献   

7.
Germinability and virulence of sclerotia of Sclerotium rolfsii were assessed after 50 days of exposure of 14C-labeled sclerotia to soil at 0, −5 and −15 kPa and pH 6.9, or to soil at 15, 25 or 30 °C, pH 5 or 8 and −1 kPa. Evolution of 14CO2 accounted for the greatest share of endogenous carbon loss from sclerotia under all soil conditions, except in water-saturated soil (0 kPa), in which sclerotial exudates contributed the major share of carbon loss. Total evolution of 14CO2 from sclerotia in soil at −15 kPa (42.4% of total 14C) and at −5 kPa (38%) was significantly higher than at 0 kPa (23.8%). Evolution of 14CO2 in soil at 25 or 30 °C was more rapid than at 15 °C with regardless of pH. Loss of endogenous carbon by sclerotia was the greater after 50 days of exposure to soil at 0 kPa, or at 25 or 30 °C and pH 8, than at other soil conditions. Sclerotia exposed to water-saturated soil (0 kPa) showed a more rapid decline in nutrient independent germinability, viability and virulence, than to those exposed to −5 or −15 kPa. Sclerotia became dependent on nutrient for germination and lost viability and virulence within 30–40 days in soil at 25 or 30 °C, pH 8. However, more than 60% of sclerotia retained viability in soil at 15 °C regardless of pH, even after 50 days. Radish shoot growth was increased significantly by the sclerotia that had been exposed to soil at 0 kPa, or to soil at 25 or 30 °C and pH 8 for 50 days. In conclusion, carbon loss by sclerotia during incubation on soil at different pH levels, temperatures and water potentials was inversely correlated with sclerotial ability to infect radish seedlings. The relationship between carbon loss by sclerotia and radish shoot length was positive.  相似文献   

8.
《Applied soil ecology》2006,33(3):284-292
We examined the response of the temperature coefficient (Q10) for soil respiration to changes in soil temperature and soil moisture through a laboratory incubation experiment. Two types of soils differing in vegetation and moisture status were collected and incubated under two temperatures (10 and 30 °C) and two soil moisture regimes (35 and 75% of water holding capacity, WHC) for 5 weeks. Before and after the incubation experiment, the temperature coefficient of soil respiration was measured using soda-lime method by changing temperature in a water bath. For both soils, the mean Q10 values of the respiration rate were 2.0 in the 30 °C and 2.3 in the 10 °C soil treatments. Higher temperature with lower soil moisture treatment significantly decreased the Q10 value, whereas lower temperature with higher soil moisture treatment significantly enhanced the Q10 value (ANOVA, p < 0.05). These results indicate that soils became less sensitive to temperature when incubated under higher temperature with higher moisture conditions, and more sensitive in lower temperature with higher moisture conditions.There was a significant correlation (r2 = 0.67, p < 0.05) between water-soluble carbon (WSC) and soil respiration rate. However, the correlation between soil respiration rate and microbial biomass carbon (MBC) was weak (r2 = 0.27, p > 0.05). Although incubation temperature and moisture accounted for 40 and 29% (as r2 × 100%), respectively, of variations in Q10, soil water-soluble carbon content alone could have explained 79% of the variation, indicating that the availability of respiratory substrate, rather than the pool of soil microorganisms, played a crucial role in the response of the temperature coefficient to environmental factors. These results suggest that biotic factors should also be taken into consideration when using the Q10 function to predict the response of soil respiration to global warming.  相似文献   

9.
《Applied soil ecology》2003,22(3):205-210
We examined the response of the temperature coefficient (Q10) for soil respiration rate to changes in environmental temperature through a laboratory incubation experiment. Soil samples were collected from three climatic areas: arctic (Svalbard, Norway), temperate (Tsukuba, Japan) and tropical (Pasoh, Malaysia). The arctic and temperate soils were incubated at 8 °C (control), 12 °C (4 °C warming) and 16 °C (8 °C warming) for 17 days. The tropical soil was incubated at 16 °C (8 °C cooling), 24 °C (control) and 32 °C (8 °C warming). Before and after the incubation experiment, the temperature dependence of soil microbial respiration was measured using an open-airflow method with IRGA by changing the temperature in a water bath. The initial Q10 before the incubation experiment was larger in the soils from higher latitudes: 3.4 in the arctic soil, 2.9 in the temperate soil, and 2.1 in the tropical soil. The response of the microbial respiration rate to change in temperature differed among the three soil types. The temperature dependence of respiration rate in the arctic soil did not change in response to warming by 4 and 8 °C with a Q10 of about 3. On the other hand, the Q10 in the temperate soil decreased with increasing incubation temperature: from 2.8 in soils incubated at 8 °C to 2.5 at 12 °C and 2.0 at 16 °C. In the tropical soil, the Q10 was not changed even by the 8 °C warming with a value of 2.1, whereas the Q10 was increased from 2.1 to 2.7 by the 8 °C cooling. These results suggest that the response of microbial respiration to climatic warming may differ between soils from different latitudes.  相似文献   

10.
The rate of organic matter turnover in soil is a critical component of the terrestrial carbon cycle and is frequently estimated from measurements of respiration. For estimates to be reliable requires that isotopically labelled substrate uptake into the soil microbial biomass and its subsequent mineralization occurs almost simultaneously (i.e. no time delay). Here we investigated this paradigm using glucose added to an agricultural soil. Immediately after collection from the field, various concentrations of 14C-labeled glucose (1 μM to 10 mM) were added to soil and the depletion from the soil solution measured at 1–60 min after substrate addition. 14CO2 production from the mineralization of glucose was simultaneously measured. The microbial uptake of glucose from soil solution was concentration-dependent and kinetic analysis suggests the operation of at least two distinct glucose transport systems of differing affinity. At glucose concentrations reflecting those naturally present in the soil solution (54±10 μM), the half-time (t1/2) of exogenous glucose was extremely rapid at ca. 30 s. At higher glucose concentrations (100 μM to 10 mM), the t1/2 values for the high-affinity carrier were altered little, but increasing proportions of glucose were taken up by the low affinity transport system. Glucose mineralization by the soil microbial community showed a significant delay after its uptake into the microbial biomass suggesting a decoupling of glucose uptake and subsequent respiration, possibly by dilution of glucose in labile metabolite pools. By fitting a double first order kinetic equation to the mineralization results we estimated the t1/2 for the first rapid phase of respiration at natural soil solution glucose concentrations to be 6–8 min, but at least 87% of the added glucose was retained in the microbial biomass prior to mineralization. Our results suggest that in this soil the soil solution glucose pool turns over 100–1000 times each day, an order of magnitude faster than when determined from measurements of mineralization. These results imply that traditional isotopic based measurements of substrate turnover measured using CO2 may vastly underestimate their rate of cycling in soil.  相似文献   

11.
《Applied soil ecology》2001,16(3):243-249
Very little is known about the effect of overgrazing on carbon loss from soil in semi-arid savannas and woodlands of South America. Soil carbon parameters were measured in a 10,000 ha restoration project in the western Chaco of Argentina (24°43′S and 63°17′W). Three situations were compared: highly restored (HRS), moderately restored (MRS) and highly degraded (HDS). Soil and litter samples were recovered in the dry and wet seasons. SOC and CO2–C values decreased from the HRS (7.0 kg m−2 and 130 g m−2) to the HDS (1.5 kg m−2 and 46 g m−2) whereas the C mineralization rate increased toward the less restored sites (0.96–2.29). Surface-litter C was similar in both sites under restoration (260 and 229 g m−2), being non-existent at the HDS. Leaves from woody species dominated surface-litter in the HRS, whereas grass material was predominant in the MRS. During the wet season, the SOC decreased, whereas both CO2–C and C mineralization rate increased. The magnitude of the between-season differences was highest at the HDS (62% in SOC, 55% in CO2, and 80% in C mineralization rate). We estimated that C loss since introduction of cattle into the forest was 58 Mg ha−1, reaching a total of 2×1015 g at for the entire Chaco. These values are higher than those caused by the conversion of savannas and other ecosystems into agriculture or cultivated pastures. The amount of C fixed in the highly restored site (275 g ha−1 per year) indicates that the Chaco soils have a significant potential as atmospheric carbon sinks.  相似文献   

12.
《Applied soil ecology》2010,46(3):187-192
The influences of winter climate on terrestrial ecosystem processes have been the subject of growing attention, which is necessary to make the predictions about ecological responses to global warming in the future. However, little information can be found about the impacts of a large range of soil temperature fluctuation (e.g. −10 to 5 °C) over winter on the soil nitrogen (N) dynamics in the field. In the present study, we employed an intact soil core in situ incubation technique, and measured soil N mineralization and nitrification rates under three plant communities, i.e. a grassland, a shrub and a plantation, during the non-growing season (October 2004–April 2005) in Inner Mongolia, China. Our results demonstrate the significant effects of different plant communities on soil net N mineralization and the great temporal variations of soil N dynamics during the incubation period. The mean soil net N mineralization rates were 0.93, 0.77 and −1.28 mg N m−2 d−1, respectively, in the grassland, shrub and plantation. The mean soil NH4+-N in the three plant communities declined by 40%, but the mean soil NO3-N increased by 190% by the end of the incubation compared with their initial concentrations at the beginning of incubation. The differences in plant communities significantly affected their soil N mineralization rates, accumulations and turnover rates, which followed the order: grassland > shrub > plantation. During the winter time, the studied soils experienced the three phases consisting of mild freezing (−7 to −2 °C soil), deep freezing (approximately −10 °C soil) and freeze–thaw (−2 to 5 °C soil). The results suggest that temporal variations of soil N mineralization are positively affected by the soil temperature and the soil nitrification is dominant in the N transformation process during the non-growing season. Our study indicates that the soil N mineralization over winter can make a substantial contribution to the mineral N pool that plants are able to utilize in the upcoming spring, but may also pose a great risk of mineral N leaching loss if great rainfalls occur during spring and early summer.  相似文献   

13.
The herbicide, glyphosate [N-(phosphonomethyl) glycine] is extensively used worldwide. Long-term use of glyphosate can cause micronutrient deficiency but little is known about potassium (K) interactions with glyphosate. The repeated use of glyphosate may create a selection pressure in soil microbial communities that could affect the nutrient dynamics such as K. The objective of this study was to determine the effect of single or repeated glyphosate applications on microbial and K properties of soils. A 54 day incubation study (Exp I) had a 3 × 5 factorial design with 3 soils (silt loam: fine, illitic, mesic Aeric Epiaqualf) of similar physical and chemical characteristics, that varied in long-term glyphosate applications (no, low, and high glyphosate field treatments) and five glyphosate rates (0, 0.5×, 1×, 2×, and 3× recommended field rates applied once at time zero). A second 6 month incubation study (Exp II) had a 3 × 3 factorial design with three soils (as described above) and three rates of glyphosate (0, 1×, and 2× recommended field application rates applied monthly). For each study microbial properties [respiration; community structure measured by ester linked fatty acid methyl ester (EL-FAME) analysis and microbial biomass K] and K fractions (exchangeable and non-exchangeable) were measured periodically. For Exp I, glyphosate significantly increased microbial respiration that was closely related to glyphosate application rate, most notably in soils with a history of receiving glyphosate. For Exp II, there was no significant effect of repeated glyphosate application on soil microbial structure (EL-FAME) or biomass K. We conclude that glyphosate: (1) stimulates microbial respiration particularly on soils with a history of glyphosate application; (2) has no significant effect on functional diversity (EL-FAME) or microbial biomass K; and (3) does not reduce the exchangeable K (putatively available to plants) or affect non-exchangeable K. The respiration response in soils with a long-term glyphosate response would suggest there was a shift in the microbial community that could readily degrade glyphosate but this shift was not detected by EL-FAME.  相似文献   

14.
《Applied soil ecology》2009,41(3):529-535
The repeated introduction of an organic resource to soil can result in its enhanced degradation. This phenomenon is of primary importance in agroecosystems, where the dynamics of repeated nutrient, pesticide, and herbicide amendment must be understood to achieve optimal yield. Although not yet investigated, the repeated introduction of cadaveric material is an important area of research in forensic science and cemetery planning. It is not currently understood what effects the repeated burial of cadaveric material has on cadaver decomposition or soil processes such as carbon mineralization. To address this gap in knowledge, we conducted a laboratory experiment using ovine (Ovis aries) skeletal muscle tissue (striated muscle used for locomotion) and three contrasting soils (brown earth, rendzina, podsol) from Great Britain. This experiment comprised two stages. In Stage I skeletal muscle tissue (150 g as 1.5 g cubes) was buried in sieved (4.6 mm) soil (10 kg dry weight) calibrated to 60% water holding capacity and allowed to decompose in the dark for 70 days at 22 °C. Control samples comprised soil without skeletal muscle tissue. In Stage II, soils were weighed (100 g dry weight at 60% WHC) into 1285 ml incubation microcosms. Half of the soils were designated for a second tissue amendment, which comprised the burial (2.5 cm) of 1.5 g cube of skeletal muscle tissue. The remaining half of the samples did not receive tissue. Thus, four treatments were used in each soil, reflecting all possible combinations of tissue burial (+) and control (−). Subsequent measures of tissue mass loss, carbon dioxide-carbon evolution, soil microbial biomass carbon, metabolic quotient and soil pH show that repeated burial of skeletal muscle tissue was associated with a significantly greater rate of decomposition in all soils. However, soil microbial biomass following repeated burial was either not significantly different (brown earth, podsol) or significantly less (rendzina) than new gravesoil. Based on these results, we conclude that enhanced decomposition of skeletal muscle tissue was most likely due to the proliferation of zymogenous soil microbes able to better use cadaveric material re-introduced to the soil.  相似文献   

15.
《Applied soil ecology》2007,35(3):553-565
The underlying influences of soil flooding, pH level and soil-inhabiting Diaprepes abbreviatus (L.) root weevil larval feeding in citrus were examined in two separate greenhouse studies, rootstock × flooding × Diaprepes-larvae (RFD) and liming × rootstock × flooding × Diaprepes-larvae (LRFD). Our objectives were to determine the combined effects of soil flooding and pH level on survival and growth of Diaprepes root weevil larvae to gain insights of insect-environmental relations for the weevil control. We used a Floridana sandy loam (pH 4.8) from a citrus grove infested by Diaprepes root weevil in center Florida. The RFD experiment consisted of two citrus rootstocks (Swingle and Smooth Flat Seville), three flooding durations (0, 20, and 40 days) and two larval infestation rates (0 and 5 larvae) for 40-day feeding. The LRFD experiment consisted of two citrus rootstocks (Swingle and Carrizo), three pH levels (non-limed control, and target pH 6 and 7), two flooding durations (0 and 40 days), and two larval rates (0 and 5 larvae) for 56-day feeding. Dolomite (54% CaCO3 and 46% MgCO3) was used for soil liming in the LRFD. Treatments were arranged with 15 replicates in a completely randomized design. In the RFD, flooded soil pH was 0.3 units higher than non-flooded soil and larval survival was the lowest in the longest flooded treatment (P < 0.05). In the LRFD, soil pH increased 0.5–0.9 units for the target pH 6, and 0.7–1.1 units for the target pH 7. The effects of rootstock, liming and flooding treatments and their interactions were significant on soil pH and larval survival (P < 0.05). Larval survival decreased from 80% to 60% with increasing soil pH from 4.8 to 5.7. Total larval weight per seedling decreased significantly from 0.060 g to 0.012 g when the soil pH increased from 5.1 to 5.7. Flooding reduced larval survival and growth, and increasing acidic soil pH by 1 unit would be an option for controlling soil acidity and for promoting integrated management of Diaprepes root weevil in citrus.  相似文献   

16.
Meat and bone meal (MBM) utilization for animal production was banned in the European Union since 2000 as a consequence of the appearance of transmissive spongiform encephalopathies. Soil application could represent a lawful and effective strategy for the sustainable recycling of MBM due to its relevant content of nutritive elements and organic matter. The effectiveness of MBM as organic fertilizer needs to be thoroughly investigated since there is a lack of knowledge about the mineralization dynamics of MBM in soil and the impact of such residues, in particular the high content of lipids, on soil biochemical and microbiological properties. For this aim, a defatted (D) and the correspondent non-defatted (ND) MBM were added at two rates (200 and 400 kg N ha?1) to two different moist soils and incubated at 15 and 20 °C for 14 d. MBM mineralization dynamics was studied by measuring CO2 evolution. Water extractable organic C, K2SO4-extractable NO3? and NH4+, microbial biomass ninhydrin-reactive N, enzymatic activities (FDA, urease, protease, alkaline phosphatase) and microbial composition (aerobic and anaerobic bacteria, fungi) were measured 2 and 14 d after MBM addition to the soil. The rate of CO2 evolution showed a maximum 2–3 d after the addition of MBM, followed by a decrease approaching the control. MBM mineralization was fast with, on average, 54% of total CO2 evolved in the first 4 d of incubation at 20 °C. The percentage of added C which was evolved as CO2 at the end of the incubation period ranged between 8% and 16% and was affected by temperature, soil type and MBM treatment (ND > D). Soil amendment with MBM caused a noteworthy increase in both extractable NH4+ and NO3? (about 50% of added N) which was higher for ND. The addition of MBM also enhanced microbial content and activity. Microbial biomass increased as a function of the rate of application and was higher for ND with respect to D. The increase in numbers of aerobic and anaerobic bacteria and fungi caused by MBM addition was, in general, more pronounced with ND. Enzymatic activity in amended soils showed an enhancement in nutrient availability and element cycling. At the rate of application of present work, lipids did not cause adverse effects on soil microorganisms.The potential of MBM as effective organic fertilizer was supported by the large increase in available N and the enhancement of the size and activity of soil microorganisms.  相似文献   

17.
The substrate availability for microbial biomass (MB) in soil is crucial for microbial biomass activity. Due to the fast microbial decomposition and the permanent production of easily available substrates in the rooted top soil mainly by plants during photosynthesis, easily available substrates make a very important contribution to many soil processes including soil organic matter turnover, microbial growth and maintenance, aggregate stabilization, CO2 efflux, etc. Naturally occurring concentrations of easily available substances are low, ranging from 0.1 μM in soils free of roots and plant residues to 80 mM in root cells. We investigated the effect of adding 14C-labelled glucose at concentrations spanning the 6 orders of magnitude naturally occurring concentrations on glucose uptake and mineralization by microbial biomass. A positive correlation between the amount of added glucose and its portion mineralized to CO2 was observed: After 22 days, from 26% to 44% of the added 0.0009 to 257 μg glucose C g?1 soil was mineralized. The dependence of glucose mineralization on its amount can be described with two functions. Up to 2.6 μg glucose C g?1 soil (corresponds to 0.78% of initial microbial biomass C), glucose mineralization increased with the slope of 1.8% more mineralized glucose C per 1 μg C added, accompanied by an increasing incorporation of glucose C into MB. An increased spatial contact between micro-organisms and glucose molecules with increasing concentration may be responsible for this fast increase in mineralization rates (at glucose additions <2.6 μg C g?1). At glucose additions higher than 2.6 μg C g?1 soil, however, the increase of the glucose mineralization per 1 μg added glucose was much smaller as at additions below 2.6 μg C g?1 soil and was accompanied by decreasing portions of glucose 14C incorporated into microbial biomass. This supports the hypothesis of decreasing efficiency of glucose utilization by MB in response to increased substrate availability in the range 2.6–257 μg C g?1 (=0.78–78% of microbial biomass C). At low glucose amounts, it was mainly stored in a chloroform-labile microbial pool, but not readily mineralized to CO2. The addition of 257 μg glucose C g?1 soil (0.78 μg C glucose μg?1 C micro-organisms) caused a lag phase in mineralization of 19 h, indicating that glucose mineralization was not limited by the substrate availability but by the amount of MB which is typical for 2nd order kinetics.  相似文献   

18.
Polar ecosystems are currently experiencing some of the fastest rates of climate warming. An increase in soil temperature in High Arctic regions may stimulate soil permafrost melting and microbial activity, thereby accelerating losses of greenhouse gases. It is therefore important to understand the factors regulating the rates of C turnover in polar soils. Consequently, our aims were to: (1) assess the concentration of low molecular weight (MW) dissolved organic carbon (DOC) in soil, (2) to investigate the temperature-dependent turnover of specific low MW compounds, and (3) to analyse the influence of substrate concentration on C cycling. Microbial mineralisation of labile low MW DOC in two High Arctic tundra soils was investigated using soil solutions spiked with either 14C-labelled glucose or amino acids. Spiked solutions were added to the top- and sub-soil from two ecosystem types (lichen and Carex dominated tundra), maintained at three temperatures (4–20 °C), and their microbial mineralisation kinetics monitored. 14CO2 evolution from the tundra soils in response to 14C-glucose and -amino acid addition could best be described by a double first order exponential kinetic equation with rate constants k1 and k2. Both forms of DOC had a short half-life (t1/2) in the pool of microbial respiratory substrate (t1/2 = 1.07 ± 0.10 h for glucose and 1.63 ± 0.14 h for amino acids; exponential coefficient k1 = 0.93 ± 0.07 and 0.64 ± 0.06 h?1 respectively) whilst the second phase of mineralisation, assumed to be C that had entered the microbial biomass, was much slower (average k2 = 1.30 × 10?3 ± 0.49 × 10?4 h?1). Temperature had little effect on the rate of mineralisation of 14C used directly as respiratory substrate. In contrast, the turnover rate of the 14C immobilized in the microbial biomass prior to mineralisation was temperature sensitive (k2 values of 0.99 × 10?3 h?1 and 1.66 × 10?3 h?1 at 4 and 20 °C respectively). Concentration-dependent glucose and amino acid mineralisation kinetics of glucose and amino acids (0–10 mM) were best described using Michaelis–Menten kinetics; there was a low affinity for both C substrates by the microbial community (Km = 4.07 ± 0.41 mM, Vmax = 0.027 ± 0.005 mmol kg?1 h?1). In conclusion, our results suggest that in these C limiting environments the flux of labile, low MW DOC through the soil solution is extremely rapid and relatively insensitive to temperature. In contrast, the turnover of C incorporated into higher molecular weight microbial C pools appears to show greater temperature sensitivity.  相似文献   

19.
A short-term incubation study was carried out to investigate the effect of biochar addition to soil on CO2 emissions, microbial biomass, soil soluble carbon (C) nitrogen (N) and nitrate–nitrogen (NO3–N). Four soil treatments were investigated: soil only (control); soil + 5% biochar; soil + 0.5% wheat straw; soil + 5% biochar + 0.5% wheat straw. The biochar used was obtained from hardwood by pyrolysis at 500 °C. Periodic measurements of soil respiration, microbial biomass, soluble organic C, N and NO3–N were performed throughout the experiment (84 days). Only 2.8% of the added biochar C was respired, whereas 56% of the added wheat straw C was decomposed. Total net CO2 emitted by soil respiration suggested that wheat straw had no priming effect on biochar C decomposition. Moreover, wheat straw significantly increased microbial C and N and at the same time decreased soluble organic N. On the other hand, biochar did not influence microbial biomass nor soluble organic N. Thus it is possible to conclude that biochar was a very stable C source and could be an efficient, long-term strategy to sequester C in soils. Moreover, the addition of crop residues together with biochar could actively reduce the soil N leaching potential by means of N immobilization.  相似文献   

20.
《Applied soil ecology》1999,11(1):91-101
Potential C and N mineralization and soil microbial biomass C (SMBC) are soil biological properties important in understanding nutrient and organic matter dynamics. Knowledge of soil water content at a matric potential near field capacity is needed to determine these biological properties. The objective of this study was to examine whether adjustment of soil water content to a common level of water-filled pore space (WFPS) may be an acceptable alternative that would require little prior analysis in comparison with adjustment based on matric potential. Potential C and N mineralization and SMBC were determined from 15 variably eroded soils of the Madison–Cecil–Pacolet association (clayey, kaolinitic, thermic Typic Kanhapludults) in response to WFPS. The levels of WFPS to achieve maximum activity and biomass under naturally settled conditions were unaffected by clay content and occurred at 0.42±0.03 m3 m−3 for net N mineralization during 24 days of incubation, 0.51±0.22 m3 m−3 for specific respiratory activity of SMBC, 0.60±0.07 m3 m−3 for cumulative C mineralization during 24 d of incubation, and 0.76±0.27 m3 m−3 for SMBC. Selecting a common WFPS level of 0.5 m3 m−3 resulted in 96±2%, 97±5%, 97±4%, and 88±10% of the maximum for these four properties, respectively, and was a reasonable compromise when attempting to estimate these properties during simultaneous incubations. Adjusting soil water content based on WFPS was simpler and nearly as reliable as based on matric potential, in which soil water content at −33 kPa varied from 0.16 to 0.30 g g−1.  相似文献   

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