阴离子对可变电荷土壤吸附铜离子的影响机理

根据NO-3、Cl-和SO24-对可变电荷土壤和恒电荷土壤吸附Cu2+的影响的比较,探讨了阴离子对可变电荷土壤吸附Cu2+的影响机理。结果表明,当3种阴离子的浓度相同时,在SO24-体系中铁质砖红壤对Cu2+的吸附率较在NO3-和Cl-体系中大得多,而在浓度相同的3种阴离子体系中,黄棕壤对Cu2+的吸附率相差不大。在离子强度相近的NaCl体系中,砖红壤对Cu2+的吸附率相近。在3种阴离子体系中,随着pH升高,砖红壤对Cu2+的吸附率均增大;但在NO-3体系和Cl-体系中Cu2+的吸附率相近;而在SO24-体系中Cu2+的吸附率最大。随着Na2SO4浓度的增大,铁质砖红壤和砖红壤对Cu2+的吸附率减小。但在0.005 mol L-1和0.05 mol L-1Na2SO4体系中,Cu2+的吸附率大于在不含Na2SO4的体系中者。而在0.5 mol L-1Na2SO4体系中,Cu2+吸附率小于在不含Na2SO4体系中者。在3种浓度的Na2SO4体系中,黄棕壤对Cu2+的吸附率均小于在不含Na2SO4体系中者。总之,阴离子可通过离子强度、专性吸附和形成离子对影响土壤对Cu2+的吸附。在可变电荷土壤中,阴离子对Cu2+吸附的影响机理较在恒电荷土壤中复杂得多。     

基于BP神经网络的不同人为干扰强度下盐渍土SO42-定量分析

SO_4~(2-)是盐渍土阴离子中的主要离子,但目前针对不同人为干扰区域土壤中SO_4~(2-)反演研究却鲜有报道。土壤高光谱与土壤某元素间的关系表现为非线性,传统线性偏最小二乘模型(PLSR)对土壤元素的反演精度有限。本文以新疆昌吉回族自治州境内不同人为干扰区域的盐渍化土壤为研究对象,以土壤的野外高光谱和SO_4~(2-)含量为数据源,对原始(R)和对数(LogR)变换后的高光谱分别进行0阶、一阶和二阶微分预处理,选择通过0.05显著性水平的波段为敏感波段,将敏感波段对应的高光谱反射率作为非线性BP神经网络模型的输入变量,并设定BP的隐藏节点为300,学习速率为0.01,最大迭代次数为1 000,训练函数为trainscg。从SO_4~(2-)的真实值与预测值的散点图、拟合效果图和BP训练过程3个方面,定量分析无人为干扰(A区)和有人为干扰(B区)土壤SO_4~(2-)含量,并与PLSR对比预测精度。仿真显示, A区二阶微分后的BP预测精度优于一阶微分,而B区一阶微分后的BP预测精度优于二阶微分。且不论在A区还是B区, LogR光谱变换的反演精度均优于R。最佳BP模型的相对预测性能(RPD)、决定系数(R2)、均方根误差(RMSE)和迭代次数,在A区分别为3.309、0.906、0.253和8次,在B区分别为2.234、0.844、0.786和45次,表明BP对A区SO_4~(2-)的预测能力非常强(RPD2.5),对B区SO_4~(2-)的预测能力较强(RPD为2.0～2.5)。而在A区和B区两种光谱变换的一阶和二阶微分中, PLSR的RPD值均在1.4与1.8之间,其预测性能一般;在B区的0阶微分中, PLSR的RPD值均小于1.0,其不能对SO_4~(2-)进行预测。因此, BP模型能对不同人为干扰区域的SO_4~(2-)进行有效的定量分析。     

Interactions of NaCl and Na2SO4 on soil organic C mineralization after addition of maize straws

NaCl and Na₂SO₄ often dominate salt compositions in saline soils. While either salt alone affects soil organic matter mineralization, their interactions on soil organic matter dynamics are unknown. This study aimed to investigate interactive effects of the two salts on organic C mineralization and microbial biomass C of the saline soils after addition of maize straws. Both NaCl and Na₂SO₄ were applied at 0, 40 and 80 mmol Na kg⁻¹ soil and the incubation was undertaken at soil water content of 15% and 20% (w/w) in dark at 28.5 °C for 70 days. The study found significant interactions of NaCl and Na₂SO₄ on CO₂-C evolution during the early incubation periods—a suppressing effect at days 1-2 but a stimulating effect at days 6-8 and 17-20, and thereafter the salt interactions were influenced by water content. The interactions of water content with NaCl or Na₂SO₄ on CO₂-C evolution were observed through the incubation periods except days 1-2, showing that the salt effects were dependent on water content. Total CO₂ evolution over the 70-day-long incubation decreased with increasing NaCl but increased with increasing Na₂SO₄ compared to the nil-salted treatment. Salt interactions on soil microbial biomass C were observed at days 7, 21, but not at day 49. Microbial biomass C increased at day 7 in the soils treated with either NaCl or Na₂SO₄ but decreased where the two salts were combined. At day 21, microbial biomass C increased with NaCl but decreased with Na₂SO₄ regardless whether the counterpart salt was added. The results suggest that soil organic C mineralization can be affected by the interactions of NaCl and Na₂SO₄, possibly through the salt-induced changes in microbial biomass community structure.     

Mineralization of carbon and nitrogen from fresh and anaerobically stored sheep manure in soils of different texture

A sandy loam soil was mixed with three different amounts of quartz sand and incubated with (¹⁵NH₄)₂SO₄ (60 g N g^-1 soil) and fresh or anaerobically stored sheep manure (60 g g^-1 soil). The mineralization-immobilization of N and the mineralization of C were studied during 84 days of incubation at 20°C. After 7 days, the amount of unlabelled inorganic N in the manure-treated soils was 6–10 g N g^-1 soil higher than in soils amended with only (¹⁵NH₄)₂SO₄. However, due to immobilization of labelled inorganic N, the resulting net mineralization of N from manure was insignificant or slightly negative in the three soil-sand mixtures (100% soil+0% quartz sand; 50% soil+50% quartz sand; 25% soil+75% quartz sand). After 84 days, the cumulative CO₂ evolution and the net mineralization of N from the fresh manure were highest in the soil-sand mixutre with the lowest clay content (4% clay); 28% fo the manure C and 18% of the manure N were net mineralized. There was no significant difference between the soil-sand mixtures containing 8% and 16% clay, in which 24% of the manure C and -1% to 4% of the manure N were net mineralized. The higher net mineralization of N in the soil-sand mixture with the lowest clay content was probably caused by a higher remineralization of immobilized N in this soil-sand mixture. Anaerobic storage of the manure reduced the CO₂ evolution rates from the manure C in the three soil-sand mixtures during the initial weeks of decomposition. However, there was no effect of storage on net mineralization of N at the end of the incubation period. Hence, there was no apparent relationship between net mineralization of manure N and C.     

Sulfur dioxide inhibition of photosynthesis at different CO2 and O2 concentrations in relation to photorespiration

The mechanism of SO₂ inhibition of photosynthesis in intact leaves of tomato and maze was studied to evaluate SO₂ inhibition of photorespiration. Leaf tissues were fumigated with SO₂ under photorespiratory (low CO, and/or high O, concentrations) and non-photo-respiratory conditions. When tomato leaf disks were fumigated with 10 ppm SO₂ at 2, 21 and 100° o O., SO₂ inhibited photosynthesis at 2% O₂ in the same degrees as at 21% O₂. SO₂ inhibition of photosynthesis was depressed at higher CO₂ concentrations when the disks were fumigated with SO₂ at different CO₂ concentrations. High CO₂ concentrations also reduced the photosynthesis inhibition of maize leaf disks. These results suggest that SO₂ inhibits photosynthesis through other mechanisms than photorespiration inhibition and confirm the view that SO₂ competes with CO₂ for the carboxylating enzymes in photosynthesis     

Indirect determination of micrograms of sulfate by barium absorption spectroscopy

Abstract

The indirect procedure for sulfate determination by Ba absorption spectroscopy was modified so that low concentrations of SO₄ in small volumes of solutions could be determined rapidly and precisely. Major modifications consisted of seeding the sample with BaSO₄, precipitating in ethanol solutions to lower BaSO₄ solubility, and determining Ba in a N₂O‐acetylene flame using the absorption mode.

The results showed: complete SO₄ precipitation as BaSO₄ after 15 min of shaking, little or no effect from solution Al on SO₄ determination, quantitative recovery of SO₄ from 0.01 M Ca(H₂PO₄)₂ soil extracts, and greater precision of SO₄ measurement with indirect method than with turbidimetric method.     

Variation in the relationship between nitrification and acidification of subtropical soils as affected by the addition of urea or ammonium sulfate

The effects on nitrification and acidification in three subtropical soils to which (NH₄)₂SO₄ or urea had been added at rate of 250 mg N kg⁻¹ was studied using laboratory-based incubations. The results indicated that NH₄⁺ input did not stimulate nitrification in a red forest soil, nor was there any soil acidification. Unlike red forest soil, (NH₄)₂SO₄ enhanced nitrification of an upland soil, whilst urea was more effective in stimulating nitrification, and here the soil was slightly acidified. For another upland soil, NH₄⁺ input greatly enhanced nitrification and as a result, this soil was significantly acidified. We conclude that the effects of NH₄⁺ addition on nitrification and acidification in cultivated soils would be quite different from in forest soils. During the incubation, N isotope fractionation was closely related to the nitrifying capacity of the soils.     

Evidence of N<Subscript>2</Subscript>O emission and gaseous nitrogen losses through nitrification-denitrification induced by rice plants (<Emphasis Type="Italic">Oryza sativa</Emphasis> L.)

A greenhouse experiment was conducted with a specially designed apparatus consisting of an upper and lower chamber where the treatment with rice was carried out (treatment 1). The apparatus also had a single chamber where treatment 2, without rice plants, was carried out. The scope of this study was to elucidate the influence of rice plant growth on gaseous N losses as N₂ and N₂O produced by nitrification-denitrification in a flooded soil fertilized with (NH₄)₂SO₄ (with 56.50 atom% ¹⁵N). Gas samples were withdrawn weekly and analyzed for (N₂ + N₂O)-¹⁵N losses by mass spectrometer and for N₂O by gas chromatograph. The gaseous (N₂ + N₂O)-¹⁵N losses of the treatment with rice plants were significantly (P =0.01) higher than those of the treatment without rice plants, as were the amounts of N₂O emitted. Rice plants facilitate the efflux of N₂ and N₂O from soil to atmosphere, as about half of the total gaseous ¹⁵N loss as N₂ and N₂O was found in the upper chamber. The proportion of N₂O-¹⁵N to (N₂ + N₂O)-¹⁵N in the upper chamber was 10.56%, much higher than that of the lower chamber in treatment 1 and the headspace of treatment 2.     

The Leaching Behaviour and Balances of Nitrogen and Other Elements under Spring Wheat in Lysimeter Experiment 1985–92

Abstract

In a lysimeter study it was found that moderate rates of ammonium nitrate increased utilization percentages in spring wheat, and the leaching was 10% or less of added N. Over-optimal rates reduced utilization percentages and increased leaching to almost 50% of the highest doses. Late split application of calcium nitrate increased the percentage of N in grain. Furthermore, leaching of N was not reduced, but occurred somewhat later in the fall and winter seasons. Leaching of Cl^? was more rapid and that of SO₄ ^2- was delayed relative to the leaching of NO₃ ^?. Rather large negative N balances were obtained, also after over-optimal application rates, and total N content of the soil was reduced. Compared with the N₀ treatment, differences in soil N residues amounted to 15–25% of added N in seven years. Gaseous losses had apparently taken place both from the added N and from soil N according to the total-N analysis.     

Potassium recirculation in tomato plants in relation to potassium supply

The Ben Zioni ‐ Dijkshoorn hypothesis that NO₃ uptake by roots is regulated by NO₃ assimilation in the shoot was tested using the tomato plant. Plants were grown at three K levels and the fate of anion charge from NO₃,^‐ and SO₄ ^2‐. assimilation followed in its distribution between organic acid anion accumulation and HCO₃ ^‐ efflux into the nutrient medium. For the high K treatment almost all of this charge was directed towards organic acid accumulation with HCO₃ ^‐ efflux accounting for only 3% of the total charge. On the other hand for plants supplied at the low K level, a substantial proportion of the anion charge was excreted as HCO₃ ^‐ (32%).

Xylem sap analyses and NO₃ reductase assay results indicated that in the tomato plant the upper plant parts constituted the major site for NO₃ reduction. The quantitatively most important ionic constituents in the sap were K⁺, Ca²⁺ and NO₃ ^‐.

Results have been presented that indicate that when K is in short supply in the nutrient medium, K recycling occurs within the plant to facilitate the upward transport of NO₃ ^‐ from root to shoot.     

几种主要CO2施肥肥源性能的比较与评价

在空闲拱棚和黄瓜日光温室内，分别研究了化学反应法(H₂SO₄+NH₄HCO₃）、煤球燃烧法和颗粒CO₂气肥3种肥源的性能，并与液体CO₂进行成本比较，结果表明：化学反应法产气迅速，设备折旧成本较低；煤球燃烧法产气速度中等，原料成本最低；颗粒CO₂气肥产气速度较慢且不易调控，原料成本最高。考虑化学反应产物的再利用因素，化学反应法、煤球燃烧法和液体CO₂ 3种肥源总成本接近，但从生态、节能、成本和效果等方面综合评价，煤球燃烧法原料丰富、成本低廉，较符合我国目前的设施、经济、资源和技术条件。     

Nutrient Solution and Nutrient Soil Solution Parameter Evolution in Tomato with Dynamic Fertigation under Saline Conditions

This trial was carried out to study the evolution of the nutrient parameters of the nutrient solution applied to tomato plants (Lycopersicum sculentum Mill. Forteza) cultivated in Mediterranean greenhouse conditions under different fertigation management models. The dynamic model is based on soil water content, which was measured by tensiometers, and on soil solutions obtained with suction cups (porous ceramic cup water samplers). The local traditional method consists of following technical recommendations, and the classical model requires the estimation of Crop Factor (Kc) and knowing the nutrient extraction. Nutrient solution and water applied are functions of the fertigation management criteria. The water used for fertigation was classified as C₄-S₃ according to the Riverside classification system. The cultivation period lasted from 15 August to 20 April. The nutrient parameters studied in nutrient and soil solution were pH, electrical conductivity (EC), nitrate (NO₃ ^?), phosphate (H₂PO₄ ^?), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), sodium (Na⁺), and chloride (Cl^?). The pH shows similar trends under the different treatments. Electrical conductivity is in the range of 2.8–4.5 dS m^?1. Chloride, sodium, magnesium, and sulfate are exclusively modified by the salt concentration in the irrigation water, so it can be assumed that the three treatments vary equally. Nitrate, potassium, phosphate, and calcium are modified depending on each fertigation management method. Soil solution is modified by the nutrient solution applied. Dynamic management allows low nutrient concentration in the nutrient solution to be maintained and keeps soil nutrient concentration low, reducing fertilizer losses and therefore aquifer contamination.     

Effect of Chloride and Sulfate Salinity on Micronutrients Release and Uptake from Different Composts Applied on Total Phosphorus Basis

Generation of different biowastes is increasing day by day, and ultimate load on agricultural lands has increased. Concerns over increased phosphorus (P) application with nitrogen (N)–based compost application shifted the trend to P‐based applications. But focus on only one or two nutritional elements will not serve the goals of sustainable agriculture. Full insight into nutrient availability from different composts is necessary. The need to understand the nutrient release and uptake from different composts has increased because of the use of saline irrigation water in the recent scenario of fresh water shortage. Therefore, current greenhouse studies were designed to evaluate the bioavailability and leachability of some micronutrients [calcium (Ca), magnesium (Mg), and zinc (Zn)] from different biocomposts under chloride (Cl^?) and sulfate (SO₄ ^?2) saline environment. In the first pot experiment, soil was amended with livestock compost (AC), poultry compost (PC), and composted sludge (SC) at the rate of 200 kg P ha^?1 equivalent bases. Pots were irrigated with artificial saline water of sodium chloride (NaCl) or sodium sulfate (Na₂SO₄; 60 mmol_c L^?1), and leachates were collected for Ca and Mg analysis. As composts were applied on total P bases, which left varying amounts of nutrients in each treatment, it was observed that nutrient uptake and release differed greatly regardless of the total amount applied with each compost type. Amount of Ca applied with PC (3.9 g pot^?1) was greater, but Ca concentration in leachate was greater under AC‐amended treatments. Magnesium concentration also varied greatly under compost types. Among the saline irrigation, Ca and Mg concentration in leachate increased under both saline irrigations compared to nonsaline treatment, and SO₄ ^?2 had relatively greater ionic strength to replace cations than Cl^?. Calcium, Mg, and Zn uptake by maize stem and leaves were greater from SC‐amended pots followed by PC, SC, and control. Irrespective of the salt types, Ca and Mg uptake reduced under both saline irrigations, whereas Zn uptake increased as compared to nonsaline treatment. Among the salt types, it was observed that plant growth and nutrient uptake was more influenced by Cl^? than SO₄ ^?2 saline irrigation. In the second experiment, soil was saturated with NaCl and NaSO₄ (75 mmol_c L^?1) and amended with AC. The trend of nutrient uptake under both salt types was similar to first experiment, and the results of AC amendments have been discussed. It can be inferred from the results that regardless of the total amount applied, nutrient uptake greatly varies under different composts and their availability depends upon the source rather than total amount applied. Analogously, sulfate‐dominated irrigation water can increase the leaching of Ca and Mg from root zone more than chloride.     

Determination of Trace Amounts of Cadmium Ions in Water and Plant Samples Using Ligand-Less Solid Phase Extraction-Based Modified Co3O4 Nanoparticles

In this study, a new Co₃O₄ nanoparticles (NPs) coated with sodium dodecyl sulphate (SDS) is developed for preconcentration of trace amounts of cadmium ions (Cd ²⁺) as a prior step to its determination by flame atomic absorption spectrometry (FAAS). The effects of various parameters, including pH of sample solution, amount of sorbent, flow rates of solution and eluent, sample volume, type, and least amount of the eluent for elution of the Cd ²⁺ from Co₃O₄ NPs were studied and optimized. Experimental conditions for effective separation of trace levels of the Cd ²⁺were optimized with respect to different experimental parameters in Column method. Under the best experimental conditions, the calibration curve was linear in the range of 1.0–500.0 ng.mL^?1 of cadmium (Cd) with R² = 0.999. The detection limit was 0.4ng.mL^?1 in the original solution (3S_b/m) and the relative standard deviation for eight replicate determination of 0.1µg.mL^?1 Cd was ±2.1%. The method was validated by the analysis of a certified reference material with the results being in agreement with those quoted by manufactures. The developed method was successfully applied to the extraction and determination of Cd in water and food samples with satisfactory results.     

Determination of ammonium n and nitrate n in acid permanganate solution used to absorb ammonia,nitric oxide,and nitrogen dioxide evolved from soils

Abstract

Simple steam distillation methods are described for determination of ammonium N and nitrate N in acid KMnO₄ solution used to absorb NH₃, NO and NO₂ evolved from soils. They involve use of MgO for distillation of ammonia and of FeSO₄, Ag₂SO₄, and MgO for reduction of nitrate to ammonia. The methods are rapid and precise, and they permit nitrogen‐15 analysis of NH₃‐N and (NO + NO₂)‐N evolved from soils.     

EXOGENOUS APPLICATION OF POTASSIUM DIHYDROGEN PHOSPHATE CAN ALLEVIATE THE ADVERSE EFFECTS OF SALT STRESS ON SUNFLOWER

A greenhouse experiment was conducted to examine whether foliarly applied potassium + phosphorus (K + P) in the form of monopotassium phosphate (KH₂PO₄) could mitigate the adverse effects of salt stress on sunflower plants. There were two levels of root-applied salt [0 and 150 mM of sodium chloride (NaCl)], and varying levels of KH₂PO₄ [(NS (no spray), WS (spray of water), 5 + 4, 10 + 8, 15 + 12, and 20 + 16 mg g^?1 K + P, pH 6.5] applied foliarly to 18-day old non-stressed and salt stressed sunflower plants. Salt stress adversely affected the growth, yield, photosynthetic capacity, and accumulation of mineral nutrients in the sunflower plants. However, varying levels of foliar applied KH₂PO₄ proved to be effective in improving growth and yield of sunflower under salt stress. The KH₂PO₄ induced growth in sunflower was found to be associated with enhanced photosynthetic capacity, water use efficiency and relative water contents.     

中国农村户用沼气工程建设对减排CO2、SO2的贡献——分析与预测

农村户用沼气工程是中国可再生能源建设的重点项目，可为农村居民生活提供清洁的可再生能源，该工程的建设能减轻农村环境污染，有助于部分缓解全球气候变暖的趋势。该文根据国际通用的减排量计算方法，对中国农村户用沼气替代传统生物质能和煤炭所产生的CO₂和SO₂的减排量进行了计算分析，为制定农村能源发展战略和农村环境发展规划提供参考。研究结果表明，在1996～2003年间，每年可减少CO₂排放39.76～419.39万t，减少SO₂排放2.13～6.20万t。通过对2010、2020和2050年沼气替代农村传统能源减排CO₂和SO₂量的预测，证明农村户用沼气工程的建设可以有效减少CO₂和SO₂的排放。     

Chemical fixation of ammonia to soil organic matter after application of urea

Chemical fixation of NH₃ to soil organic matter was studied in two Swedish soils with different contents of organic matter: a clay soil with 2.3% C and an organic soil with 36.6% C. ¹⁵N‐labelled urea was applied at different rates to both sterilized and non‐sterilized soils. After 10 days, the soils were extracted and washed with K₂SO₄ and determined for total N and atom% ¹⁵N excess. Urea N was recovered as non‐extractable N in sterilized soil corresponding to 9.7% of supplied ^l5N‐labelled urea in the organic soil and 2.2% in the clay soil. Since no biological immobilization is thought to occur in the sterile soil, this non‐extractable N is suggested to be chemically fixed to soil organic matter. Owing to urea hydrolysis in the clay soil, pH increased from 6.3 to 9.3 and in the organic soil from 5.7 to 6.9 and 8.8, respectively, at the low and high urea supply.     

Use of 15N isotope dilution for quantification of N2 fixation associated with roots of kallar grass (Leptochloa fusca (L.))

Summary Leptochloa fusca (L.) Kunth (kallar grass) has previously been found to exhibit high rates of nitrogen fixation. A series of experiments to determine the level of biological nitrogen fixation using ¹⁵N isotopic dilution were carried out in nutrient solution and saline soil. In the nutrient solution, E. coli inoculated plants were taken as non-nitrogen-fixing control. It was observed that nearly 60%–80% of the plant N was derived from atmospheric fixation. Estimations based on the N difference method gave much lower values (18%–35%). In experiments with saline soil which was initially sterilized with chloroform fumigation, a mixed culture of N₂-fixing rhizospheric isolates from kallar grass roots was inoculated and planted to kallar grass. Uninoculated treatments were regarded as controls. The soil was previously labelled with ¹⁵N by adding cellulose and (¹⁵NH₄)₂SO₄. The results of these studies showed fixation values of 6%–32% when estimated by ¹⁵N dilution, whereas by the N difference method 54% of the plant N was estimated to be derived from fixation. This discrepancy is due to the increase in root proliferation due to inoculation, which results in greater uptake of soil N. The distribution of ¹⁵N in different fractions of the soil-N indicted isotopic dilution due to bacterial fixation of atmospheric N₂.     

东祁连山不同高寒草地型牧草返青期土壤碳分布特征

以东祁连山高寒草地为样点,对土壤有机质、K2SO4浸提碳和微生物量碳(氯仿熏蒸浸提法)等进行了研究.结果表明:该区土壤有机质介于82.3～207.2 g·kg-1,植被类型影响土壤有机质含量.土壤K2SO4浸提碳介于23.61～138.81 mg·kg-1,分别占土壤有机质和土壤微生物量碳的0.03%～0.06%和9.97%～18.46%;灌丛草地中,高山柳草地显著低于杜鹃草地(P<0.05);草本草地中,珠芽蓼草地、沼泽草地和嵩草草地显著高于禾草草地(P<0.05).土壤微生物量碳介于156.19～1 182.84mg·kg-1,上层显著高于下层(P<0.05),除2005年沼泽草地外草本草地与灌丛草地间差异显著(P<0.05);微生物量碳对土壤有机质的贡献率介于0.19%～0.48%,禾草草地最低(0.19%),金露梅灌丛草地最高(0.48%),除珠芽蓼草地和沼泽草地外均为上层高于下层;且除禾草草地和嵩草草地外微生物量碳与土壤有机质、全氮和速效磷间呈显著(P<0.05)或极显著正相关(P<0.01),与土壤K2SO4浸提碳在灌丛草地呈显著正相关(P<0.05),在草本草地呈极显著正相关(P<0.01),与微生物量氮、磷间呈极显著正相关(P<0.01).该结果表明微生物量碳及其对土壤有机质的贡献率在草地型闻和土层间差异明显,且与土壤有机质、K2SO4浸提碳、全氮和速效磷关系密切.