A comparison of the effectiveness of various extractants for determining humus quality in a calcareous soil

Abstract

Humic substances from an Argentinian chesnut (Mollisol) soil were extracted with Na‐Dowex A‐1 resin, 0.1 N NaOH and 0.1 M Na₄P₂O₇ without decalcification and with 0.1 N NaOH after decalcification. Humic to fulvic (Ch/Cf) acid and E₄/E₆ ratios of the extracts were determined and compared.

A simpler and more rapid procedure than the classical ones for extracting and characterizing soil humus is proposed. The procedure is based on the use of a chelating resin as extractant and on the direct determination of analytical properties of humus in aliquots of the extract.     

土壤有机矿质复合体研究 Ⅶ．土壤结合态腐殖质的形成特点及其结合特征

本文系统剖析了熊毅－傅积平改进区分的土壤结合态腐殖质的形成特点，胡，富组成及其结合特征。结果表明：（１）用０．１ｍｏｌ／ＬＮａＯＨ及０．１ｍｏｌ／ＬＮａＯＨ＋０．１ｍｏｌ／ＬＮａ４Ｐ２Ｏ７混合液连续浸提的松结态（Ｈ１）和稳结态（Ｈ２）腐殖质所占的比例随土壤ｐＨ升高分别呈减少和增加趋势。统计分析显示Ｈ１与游离态铁，铝呈极显著的正相关，与交换性钙呈极显著负相关，Ｈ２则与交换性钙呈极显著正相关，而与游离     

Origin and properties of humus in the subsoil of irrigated rice paddies

Stability of humus in the plow layer soil is considered to affect the quantity and quality of dissolved organic matter leached from the plow layer soil. Therefore, a model experiment was conducted to analyze the effect of soil reduction under submerged conditions on the stability of humus in the plow layer soil. The changes in the stability of humus in the plow layer soil during submerged incubations with and without rice straw application were evaluated based on the changes in the binding type of humus. Binding type of humus in the plow layer soil was analyzed by successive extractions of organic matter with water, 0.25 M Na₂SO₄, 0.1 M Na₄P₂O₇ (pH 7.0), 0.1 M Na₄P₂O₇ (pH 10.5), and 0.1 M Na₄P₂O₇ (pH 10.5) with NaBH₄. Amounts of Fe, Mn, and Mg in each fraction were also determined to estimate the relationships between humus and metals.

The successive extraction of humus indicated that the amount of organic carbon which was extractable with the (NaBH₄ +0.1 M Na₄P₂O₇) solution decreased while that of the 0.1 M Na₄P₂O₇ (pH 7.0}-extractable organic carbon increased during submerged incubation with rice straw application. The origin of the increase in the amount of organic carbon in the Na₄P₂O₇ (pH 7.0)-extractable fraction during submerged incubation was investigated further by another incubation experiment using ¹³C-glucose as a reducing agent. Atom- 13C% analysis showed that the contribution of organic carbon derived from compounds other than glucose to the increase in the contents of humic acids and fulvic acids in the Na₄P₂O₇ (pH 7.0)-extractable fractions was ca. 80%. Therefore, it was concluded that the binding type of humus changed from (NaBH₄ + Na₄P₂O₇)-extractable to Na₄P₂O₇ (pH 7.0)-extractable humus under reducing conditions. Since the amounts of organic carbon and Fe increased in the Na₄P₂O₇ (pH 7.0)-extractable fraction and decreased in the (NaBH₄ +0.1 M Na₄P₂O₇)-extractable fraction simultaneously, iron reduction was presumably associated with the change in the binding type of humus in submerged paddy soil.     

Changes in the content and composition of humus in the sandy loamy soddy-podzolic soil in a long-term liming experiment

The effect of liming on organic matter in sandy loamy soddy-podzolic soil was studied. The study was performed on samples taken from the 50-year-long experiment established by Prof. Kornilov in 1957. It was shown that liming had almost no effect on the total humus content in the soil. The humus composition was studied using two fractionation methods of the humus substances by the Ponomareva-Plotnikova procedure. The regrouping of the humus fractions occurred due to the changes in the mobility of soil mineral components, which involved a regular increase in the content of the Ca-bound fraction of humic acids (HA-2) at the expense of the HA-1 fraction bound to the mobile forms of R₂O₃ reliable at the lime rates equivalent to the total acidity and higher. The levels of the stabilization of the different HA fractions were considered, as well as the stability of the changes in the humus composition during 50 years.     

SIZE FRACTIONATION, DISSOLUTION ANALYSIS, AND INFRA-RED SPECTROSCOPY OF HUMUS COMPLEXES IN ANDO SOILS

Eight samples of Ando soil A₁ and buried A₁ horizons of different ages were fractionated into clay-, silt-, and sand-size separates, and the yields and carbon contents of these separates were determined. The clay-size separates were subjected to two series of successive extractions, 1) 0.1 M Na₄ P₂ O₇/2% Na₂ CO₃/0.5 M NaOH and 2) dithionite-citrate/2% Na₂ CO₃/0.5 M NaOH; and to difference infra-red spectroscopy for identification of the extracted constituents. The result indicated that humus evolves from forms with a very low complexing ability for Al and Fe into forms that complex Al and Fe in the A₁ horizon, and that humus further interacts with allophane-like constituents, allophane and imogolite in the buried A₁ horizon. These reactions between humus and inorganic constituents result in formation of silt- and sand-size aggregates which are stable to sonic wave treatment, but are broken down into finer particles upon boiling with H₂ O₂.     

Interactions of nitrogen fertilizers and forest humus—i fir and black pine

In incubation experiments in the laboratory interactions of urea or NH₄NO₃ with humus from stands of fir (Abies cephalonica, Loudon) growing on soils developed from flysch (shales) and limestone and with humus from stands of black pine (pinus nigra, Arn.) growing on soils developed from peridotites, limestone and schists were investigated.Fir humus from stands on flysch and limestone and black pine humus from limestone showed nitrification but it was absent from black pine humus from stands on peridotites and on schists. Humus from stands on schists showed appreciable ammonification. Increasing concentrations of urea did not initiate nitrification in the latter type of humus. No substantial N immobilization was detected in spite of relatively high P immobilization. Increases in concentration of Ca, Mg and K occurring on incubation of humus samples were related to the ability of a humus type to nitrify rather than to concentrations of added urea-N.Urea was hydrolyzed rapidly to NH⁺₄ during contact with various types of humus, resulting in an increase of pH. Production of NH⁺₄ from urea was only minimally affected by drying the humus samples at 70°C for 20 h before incubation but was reduced to 30% at 1–5°C.     

Interactions of nitrogen fertilizers and forest humus—II. Beech and oak

Laboratory incubation experiments with and without added urea or NH₄NO₃ were performed on humus from stands of beech (Fagus silvatica) grown on soils from limestone, schists, flysch and peridotites and on humus from oak (Quercus conferta) stands on soils from limestone and schists.Beech and oak humus from stands grown on soils from limestone and flysch showed considerable nitrification with a concurrent high mobilization rate of the nutrient elements Ca, Mg and K, especially in the presence of increasing urea concentrations, but no net humus N mineralization was observed. Beech humus from stands grown on soils from schists and peridotites showed no nitrification and increasing concentrations of added urea did not modify their inability to nitrify. Non-nitrifying types of humus showed considerable ammonification but their Ca, Mg and K mobilization rates were about one-tenth those observed in nitrifying humus and were inversely correlated with urea concentrations.Exchangeable Al³⁺ and extractable Mn were present in high concentrations in the underlying inorganic soils in all cases where nitrification was absent from the overlying humus but addition of 500 parts Al³⁺ and 1000 parts Mn/10⁶ separately or in combination to a nitrifying humus failed to inhibit nitrification.An interpretation of these findings is attempted with reference to the possibility of absence of nitrification in climax vegetations and the preference of certain forest species for NH⁺₄ or NO^?₃.     

Effect of liming on organically complexed aluminum of nonallophanic Andosols from northeastern Japan

Aluminum–humus complexes are believed to be highly stable under natural conditions in nonallophanic Andosols. However, it has been shown that the aluminum complexed with humus is easily released by acidic buffer solutions and possibly controls the aluminum solubility of these soils. Thus, it is highly probable that Al–humus complexes are easily influenced by rather simple chemical treatments. We examined the effects of liming (CaCO₃ treatment) on Al–humus complexes of A and B horizons from Andosols. It was observed that liming reduced the Al release rates from soil samples with pH 3.5 acetate buffer solution and the amounts of the KCl-extractable Al, suggesting the formation of precipitation from easily exchangeable Al. A much larger decrease with liming was also obtained for 0.1 M sodium pyrophosphate-extractable Al (decrease rates of 7–52%) and 0.5 M CuCl₂-extractable Al (decrease rates of 9–43%). These results strongly indicate that liming reduces significant amounts of organically complexed Al as well as the exchangeable Al. The increase in the cation exchange capacity of soils at pH 7 after liming further suggested that the carboxyl group of humus complexed with Al was partly liberated from the Al complexation and became to develop negative charges.     

生物质炭和腐殖质对稻田土壤CH4和N2O排放的影响

为探讨生物质炭与腐殖质单独施用与配合施用对稻田土壤CH₄和N₂O气体排放以及水稻产量的影响。以浙江临安潜育性水稻土的稻田系统为研究对象,设置2个水稻秸秆生物质炭添加水平(0,20 t/hm²)和3个腐殖质水平(0,0.6,1.2 t/hm²),共6个处理,分别为:(1)B0F0(对照,不添加生物质炭和腐殖质);(2)B0F1(腐殖质用量为0.6 t/hm²);(3)B0F2(腐殖质用量为1.2 t/hm²);(4)B1F0(生物质炭用量为20 t/hm²);(5)B1F1(生物质炭和腐殖质用量分别为20,0.6 t/hm²);(6)B1F2(生物质炭和腐殖质用量分别为20,1.2 t/hm²),研究生物质炭和腐殖质输入对水稻产量、稻田CH₄和N₂O气体排放的影响。结果表明:(1)与B0F0相比,单独施用生物质炭和腐殖质或生物质炭与腐殖质配施均降低了土壤CH₄累积排放量,但增加了土壤N₂O累积排放量;(2)生物质炭处理对GWP(global warming potential)和GHGI(greenhouse gas intensity)没有显著影响(P>0.05),腐殖质处理显著降低了GWP和GHGI(P<0.05),生物质炭和腐殖质对GWP和GHGI存在显著交互作用(P<0.05);(3)与B0F0相比,单独施用生物质炭和腐殖质或者生物质炭与腐殖质配施均能在一定程度上减少单位水稻产量的温室气体排放强度(GHGI),B0F2处理的GHGI最低,表明单施腐殖质处理(腐殖质用量为1.2 t/hm²)稻田土壤的减排效果和环境效应最好。研究结果为进一步探讨稻田土壤固碳减排提供数据支撑和理论依据。     

土壤中钙结合和铁铝结合腐殖质的组成及结构特征

Calcium-bound and iron- and aluminium-bound humus extracted from different soils collected from north to south of China were characterized by chemical and spectroscopic methods. Meaningful differences in the composition and structure between them were revealed by ¹³C NMR, visible spectroscopy and elemental analysis. Results showed that the contents of carbon, hydrogen and nitrogen were higher in iron- and aluminium-bound humus than in calcium-bound humus while oxygen content in calcium-bound humus was shown to be higher. The calcium-bound humus had higher C/N and O/C ratios than iron- and aluminium-bound humus. The calcium-bound humic acid (HA1) showed higher E₄/E₆ ratios than iron- and aluminum-bound humic acid (HA2) while iron- and aluminum-bound fulvic acid (FA2) showed higher E₄/E₆ ratios than calcium-bound fulvic acid (FA1). An inverse relationship between E₄/E₆ ratios and aromaticity as determined by ¹³C NMR spectra was observed for HA and FA from black soil. The ¹³C NMR spectroscopy revealed that HA2 was more aromatic than HA1. On the other hand, FA1 exhibited a higher aromaticity than FA2.     

Soil organic matter alteration under biochar amendment: study in the incubation experiment on the Podzol soils of the Leningrad region (Russia)

Purpose

Biochar is one of the most widely used ameliorants for soil amendment, which is known as factor which rises crop yields and levels of soil biological activity. Nowadays, it is under investigated how biochar application affects the dynamics of the humic components and whole soil organic matter (SOM) and the processes of its alteration. This investigation is aimed to evaluate the influence of biochar on the content, composition, and transformation of humic acids (HAs) as the main component of the SOM.

Materials and methods

The incubation experiment was carried out on three Podzol Antric soils, with varying amounts of initial total organic carbon. The incubation time was 90 days, using biochar gravimetric doses of 0.1 and 1.0%. The biochar was produced by fast pyrolysis of birch and aspen wood at 550 °С. Humus composition was analyzed for the organic matter fractions extracted with 0.1 M NaOH (containing HAs 1 + fulvic acids (FAs) 1) and 0.1 M Na₄P₂O₇ (containing HAs 1 + FAs 1 + HAs 2 + FAs 2). Isolated HAs were characterized for their elemental composition (C, N, H, and S) and molecular composition with the use of solid-state 13C nuclear magnetic resonance (13C-NMR) techniques.

Results and discussion

We found that 0.1% of biochar amendment does not influence SOM mineralization, but 1.0% of biochar increases the mineralization by 15–18%. This process is accompanied by changes in the composition and properties of the HS. The increased proportion of HA aromatic fragments in biochar indicates an increasing of their stability. However, in soils with high humus content and a significant amount of insoluble matter, the processes of mineralization and the growth of HAs are taking place simultaneously. The replenishment of HAs could be the outcome of both the intensification of the transformation processes (mineralization and humification) of the more sustainable insoluble matter compounds and the humification of the biochar itself.

Conclusions

The influence of biochar on humification in Podzol Antric soils was revealed on the basis of incubation experiment. Both negative and positive changes under biochar in HS system were demonstrated. The active decrease of humus total contents and also the labile HS ought to qualify as negative changes. The increase of HA chemical maturity that leads to the stability of humus in whole as well as the intensive new HA formation thought to qualify as positive changes.

     

Electrophoresis and size-exclusion chromatography of humic substances extracted from detritus and soils of different geneses

Electrophoresis in 10% polyacrylamide gel in the presence of denaturants and size-exclusion chromatography in Sephadex G-75 in 7 M urea were used for the comparative analysis of humic substances isolated from a typical chernozem, soddy-podzolic soil, and chestnut soil and from the easily decomposable organic matter (plant detritus) contained in these soils. After the electrophoresis, the gel with naturally colored bands of humic substances was further stained with a dye specific for proteins by immersing into a solution containing Coomassie Brilliant Blue R-250 and CuSO₄. The electrophoretic and chromatographic analyses showed that humic substances from the soils and the corresponding detritus fractions significantly differed in the intensity of the natural color of the electrophoretic fractions, the molecular-weight distribution, and the color of the electrophoretic fractions colored by the protein-specific dye (which was first discovered in this study). The hypothesis of Tyurin and Aleksandrova suggesting that the transformation of humus sources (plant detritus) into humic substances proceeds in the direction from the high-molecular compounds to the low-molecular compounds was experimentally confirmed.     

Der Einfluß von Bewässerung und Fruchtfolge auf den Humus- und Stickstoffhaushalt sowie die Bodenproduktivität in der Gezira (Sudan)

The influence of irrigation and crop rotation on the humus and nitrogen balance and soil productivity in the Sudan Gezira . Yields of Sorghum and Cotton, but not of Dolichos increased up to 3 times from the 10th to the 30th year in an unfertilized, irrigated field experiment on a vertisol with crop rotations of Cotton, Sorghum and Dolichos, esspecially after preceding years of bare fallow. Nitrogen fixation by root nodules and asymbiotic fixation by Azotobacter and blue green algae are discussed as a cause of the increased soil productivity. In a field pot trial with 2.5 cm layers of flooded soil 75 ppm of nitrogen were fixed in 12 weeks by blue green algae. On fertilization with 0.1% K₂HPO₄ and 0.1% K₂HPO₄ + 50 ppm Na₂MoO₄ they fixed 244 and 290 ppm N respectively. Drying and reflooding the soil once to several times caused the N-fixation to decrease steadily until it stopped with weekly dryings. Strong increases and decreases of organic C and N were observed in moist and also in dry field soil in different seasons as well as short term fluctuations of organic N in dry field soil.     

Permanganate oxidation of methylated and non-methylated aquatic humus in Norway

The chemical composition of aquatic humus was investigated by permanganate oxidation. Both methylated and non-methylated samples were investigated and the results compared with those of different soil humic fractions investigated earlier.The total amount of oxidation products identified from the methylated sample was 2%, and from the non-methylated sample 0.9%. The composition of the oxidation products from methylated aquatic humus was 42% benzenecarboxylic acid methyl esters (8 different compounds), 43% methoxy-benzenecarboxylic acid methyl esters (12 compounds), 10% dimethoxy-benzenecarboxylic acid methyl esters (4 compounds), and 5% of 1, 2, 3-propanetricarboxylic acid trimethyl ester. The unmethylated aquatic humus yielded 84% benzenecarboxylic acid methyl ester (7 compounds), 7% methoxy-benzenecarboxylic acid methyl esters (2 compounds), and 9% of 1, 2, 3-propanetricarboxylic acid trimethyl ester. Three diazines isolated from methylated material were believed to be artefacts from diazomethane treatment. Two of the diazines have earlier been found by oxidation of methylated soil samples, the third, C₁₀H₁₂N₂O₆, is an oxidation product of methylated aquatic humus only.Oxidation of aquatic humus yielded more benzenecarboxylic acids and methoxy-benzenecarboxylic acids than soil humic fractions, and less dimethoxy-benzenecarboxylic acids. No aliphatic dicarboxylic acids were detected among the oxidation products of the aquatic humus.The compounds identified are mainly the same as those found by oxidation of different soil humic fractions, although their yields clearly demonstrated that the aquatic humus differed in composition from the soil fractions.     

Near-infrared characteristics of forest humus are correlated with soil respiration and microbial biomass in burnt soil

Near-infrared spectroscopy and soil physicochemical determinations (pH_H2O, organic matter content, total C content, NH _inf4 ^sup+ , total N content, cation-exchange capacity, and base saturation) were used to characterize fire-or wood ash-treated humus samples. The spectroscopic and the soil physicochemical analysis data from the humus samples were used separately to explain observed variations in soil respiration and microbial biomass C by partial least-square regression. The first regression component obtained from the physicochemical and spectroscopic characterization explained 10–12% and 60–80% of the biological variation, respectively. This suggests that information on organic material collected from near-infrared spectra is very useful for explaining biological variations in forest humus.     

土壤有机矿质复合体研究Ⅵ.胶散复合体的化学组成及其结合特征

本文研究水热条件渐变的地带性土壤中Ｇ１、Ｇ２组胶散复合体有机、无机物的化学组成及其结合特点。结果表明：Ｇ２组中铁有积累现象，游离态铁、铝氧化物含量为Ｇ２＞Ｇ１，但均随土壤类型变化。松结态腐殖质（Ｈ１）为Ｇ１＞Ｇ２，紧结态腐殖质（Ｈ３）则为Ｇ１＜Ｇ２。可提取腐殖质中，松、稳结态腐殖质之比值Ｈ１／Ｈ２和胡敏酸、富里酸之比值ＨＡ／ＦＡ，除个别土壤之外，都相关不大。Ｇ１、Ｇ２两组复合体中都含有一定数量的络     

长期施肥条件下土壤养分的动态和平衡——Ⅰ对土壤腐殖质积累及其品质的影响

长期施用有机肥和化肥,对土壤腐殖质积累和改善品质的作用研究,于1986～1991在俄罗斯季米里亚捷夫农学院等地进行。主要结果如下:.1.有机肥对土壤腐殖质的积累作用大于NPK化肥。施肥所增加的土壤腐殖质,除了砂壤土外,主要是在0～60cm土层,60cm以下土层施肥效果不明显。.2.长期施用有机肥和NPK化肥,提高了胡敏酸组分Ⅰ(游离的及与活性R₂O₃结合态)的含量和腐殖酸相对迁移率,而与Ca⁺⁺离子结合的胡敏酸组分Ⅱ含量下降。由于胡敏酸组分Ⅱ与Ca⁺⁺离子结合减弱,增加了腐殖质在水中的溶解,使之在大雨或大量灌水时易于淋失。.3.施用有机肥和NPK化肥,水溶性腐殖物质的含量明显提高,缓解了干旱条件下土壤高浓度矿物盐的影响。.4.长期施肥提高了土壤的亲水性;其膨胀容积、膨胀速度常数、土壤吸水量、土壤表面积等指标均不同程度的提高,但砂壤土增加了幅度低于粉砂壤土和粘壤土。.5.胡敏酸甲氧基功能团的含量多寡是衡量土壤腐殖质化的重要指标。试验表明,长期施肥下低肥力酸性土壤中胡敏酸甲氧基含量提高了46％～300％,高肥力非酸性土壤提高了17％～32％。     

The wood-decaying fungus Hygrophoropsis aurantiaca increases P availability in acid forest humus soil, while N addition hampers this effect

We evaluated the influence of the brown rot fungus Hygrophoropsis aurantiaca on P solubility in the humus layer of a podzolic forest soil. This fungus is known to exude large amounts of oxalic acid that may stimulate weathering of minerals and increase dissolution of humus, which in turn may increase P availability in the soil surrounding the fungus. Humus was inoculated using small wooden pieces colonised by the fungus. The presence of the fungus resulted in elevated concentration of PO₄⁻ in the humus solution. In a second experiment birch seedlings grown in the same humus were able to utilise the PO₄⁻ mobilised by the fungus to increase their internal P content. The factor determining this increased P uptake and the increased available P might be oxalate produced by fungus. The acid may directly dissolve P or change organic forms of P making it more susceptible to reaction with phosphatases. This fungal effect on P solubility diminished when N was added to the soil in the form of a slow release N fertilizer (methyl urea), or when a soil with a higher soil N concentration was used. We found a strong correlation between NH₄⁺ concentration and total organic carbon in the soil solution at high NH₄⁺ concentrations, suggesting the dissolution of humus as a result of the high NH₄⁺ content in the solution. This study demonstrates that the wood-decaying fungus H. aurantiaca influences nutrient turnover in forest soil, and thereby nutrient uptake by forest trees. An intensified harvest of forest products such as whole tree harvesting may decrease the active biomass of the wood decomposers and may thereby change the availability of P and the leaching of N.     

Distribution of Zinc,Manganese, Copper,Cobalt, and Nickel in Andosols Profiles

The distribution of zinc, manganese, copper, cobalt, and nickel in Andosols was investigated. Sixty nine soil samples were collected from different horizons of an Andosols profile in Miyakonojo Basin in south Kyushu, Japan, The total contents of heavy metals were determined by digestion and four extraction solutions, 1 M NH₄Ac (ammonium acetate) pH 4.5, 0.1 M HCl, 0.01 M EDTA (ethylenediaminetetraacetic acid) pH 6.5, and 0.005 M DTPA (diethylenetri-aminepentaacetic acid) pH 7.3 were used to determine the contents of available Zn, Mn, Cu, Co, and Ni in Andosols in relation to the organic carbon content. The results of the extraction analysis showed that by the use of 0.1 M H Cl high value of extracted heavy metals in the upper layers of the humus horizons were obtained while EDTA extraction yielded a large amount of the above mentioned metals in the high humus horizons. The extractable heavy metals contents were high and these metals closely related to the organic carbon content mostly in the humus horizons in the profile. Where, biocycling process may play an important role in the concentration of heavy metals. Based on the study, it was found that the total content of Zn increased towards the C horizons or pumice layers in the soil profile. Such a trend was also found in the case of the Mn content. While the Cu content in the humus horizons was much higher in the upper part of each humus horizon. According to this study the distribution of heavy metals, Cu (organic matter complexes) in the Andosols profile was more stable than that of Zn (organic matter complexes) in soils. It was shown that Zn in the surface humus horizon was enriched but that some amount was leached under buried conditions. The same phenomenon was also observed in the distribution of Mn in the profile. The movement of Co and Ni in the soil profile was limited, as evidenced by the sharp reduction in the concentrations of these two metals in buried soils.

Hence, it is concluded that the distribution of Zn, Mn, Cu, Co, and Ni was considerably higher in the humus horizons of the Andosols profiles.     

土壤有机矿质复合体研究——Ⅱ.土壤各级团聚体中有机矿质复合体的组成及其氧化稳定性

土壤团聚体的形成是一个复杂的过程,而大团聚体(直径大于0.25毫米)形成过程则更为复杂。以往,许多研究者认为有机矿质复合体是大团聚体形成的基础。但是在具体地探索那些和大团聚体形成有关的有机矿质复合体的实质,如有机质的数量,有机物质的种类,有机矿质复合体的类型等等问题时,现有的资料仍然是不充分的。不同研究者的结果并不很一致,有一些结论甚至是相互矛盾的。从而影响这一成果在生产上的广泛应用。