秸秆还田对土壤有机碳不同活性组分储量及分配的影响

通过田间试验,研究了不同秸秆还田模式下土壤溶解性有机碳(DOC)、颗粒有机碳(POC)和矿物结合有机碳(MOC)储量及其在总有机碳(TOC)中的分配比例.结果表明: 相对于翻压还田(WR),小麦秸秆覆盖还田(WM)0～20 cm耕层TOC和MOC储量显著降低,降幅为4.1%和9.7%,DOC和POC储量显著提高,增幅为207.7%和11.9%;20～40 cm犁底层TOC和POC储量显著提高.玉米秸秆覆盖还田(MM)与MR相比,犁底层TOC和MOC储量显著提高,增幅为13.6%和14.6%.小麦-玉米秸秆均覆盖还田(WM-MM)相对于均翻压还田(WR-MR),耕层TOC和MOC储量显著降低,降幅为8.5%和10.3%.玉米秸秆还田耕层TOC和POC储量显著高于小麦秸秆还田.与对照(秸秆不还田)相比,6种还田模式耕层TOC储量增幅为5.2%～18.0%,差异达显著水平;除WM和MM模式外,犁底层TOC储量显著降低(降幅8.0%～11.5%).6种还田模式下土壤耕层DOC储量及DOC/TOC比值显著降低,在WM和WM-MM还田模式下耕层POC储量显著提高、POC/TOC比值增大,WR模式的耕层MOC储量显著提高、MOC/TOC比值增大,其余3种模式耕层POC和MOC储量均显著提高.秸秆覆盖还田有利于土壤有机碳活性组分积累,翻压还田有利于较稳定性有机碳组分积累.在提高关中地区农田TOC储量方面,玉米秸秆还田好于小麦秸秆还田、小麦-玉米秸秆翻压还田好于覆盖还田.     

有机蜂蜜的开发利用现状及其前景

开发有机蜂蜜适应环保和人类追求健康的发展趋势 ,有着特殊的社会效应。综述了各国有关有机蜂蜜及其相关生产技术的标准或法律法规 ,对开发有机蜂蜜的技术研究现状做了分析 ,并提出亟待解决的问题 ,展望了有机蜂蜜的市场前景。     

TOC, TON, TOS and TOP in Rainfall, Throughfall, Litter Percolate and Soil Solution of a Montane Rainforest Succession at Mt. Kilimanjaro, Tanzania

Organic nutrients have proven to contribute significantly to nutrient cycling in temperate forest ecosystems. Still, little is known about their relevance in the tropics. In the present study, organic C, N, S and P were analysed in rainfall, throughfall, litter percolate and soil solution of a montane rainforest at Mt. Kilimanjaro, Tanzania. The aim was to determine the amounts of organic nutrients in different water pathways and to assess the influence of forest disturbance on organic nutrients by comparing mature forests, secondary forests and shrub vegetation in clearings. Concentrations of all studied elements increased from rainfall to throughfall and litter percolate and then exhibited a rapid decrease in the mineral soil. Concentrations of organic P were above the detection limit only in the litter percolate. Organic N (ON) as a fraction of total N increased from 50% in rainfall (0.19 mg l⁻¹) to 66% (0.45 mg l⁻¹) in throughfall followed by a decline to 39% in the litter percolate (0.77 mg l⁻¹) of the mature forest. Similarly, proportions of organic S and P amounted to 43 and 34%, respectively, in the litter percolate in mature forest. For ON, this proportion further decreased to less than 10% in the soil solution. The latter was probably attributable to a high sorption capacity of the studied Andisols, which led to overall low organic element concentrations in the soil solution (OC: 1.2 mg l⁻¹, ON: 0.05 mg l⁻¹ at 1 m soil depth) as compared to other temperate and tropical forest ecosystems. Organic element concentrations were higher in litter percolate and soil solution under the clearings, but there were no differences in the relative contribution of these elements. Organic nutrient forms at Mt. Kilimanjaro appeared to be much less susceptible to leaching than their inorganic forms.     

降水变率对森林土壤有机碳组分与分布格局的影响

2006年12月-2008年6月,通过加倍降水、自然降水和去除降水3种处理的人工控制试验,研究了降水变率改变对南亚热带不同演替阶段的季风常绿阔叶林、针阔叶混交林和马尾松针叶林土壤有机碳组分与空间分布格局的影响.结果表明：在3种降水强度条件下,相同森林类型的同一层次土壤总有机碳（TOC）含量差异不显著（P>0.05）;去除降水处理下土壤表层（0～10 cm）颗粒有机碳（POC）和轻组有机碳(LFOC)含量有明显的积累趋势,加倍降水和自然降水处理下增加了POC、LFOC向下层土壤（10～20 cm、20～30 cm、30～50 cm）的运输;去除降水处理下,马尾松林土壤易氧化有机碳（ROC）含量显著高于降水处理（P<0.05）;演替早期森林土壤的POC、ROC、LFOC占总有机碳的比例大于演替后期土壤,不利于土壤有机碳的存埋.森林土壤总有机碳含量变化缓慢,而其活性有机碳组分（POC、LFOC、ROC）对降水变率改变的响应更敏感.     

Organic carbon dynamics in two regulated rivers in northwestern Montana,USA

We studied the transport of particulate organic carbon (POC) and dissolved organic carbon (DOC) in two regulated rivers during minimum and increasing discharges. Mean annual concentrations of total POC, measured monthly during conditions of minimum discharge from the dams, were twice as high at a station below a dam with a selective withdrawal system on the Kootenai River (KR, 0.15 mg 1^–1), as at station below a dam with hypolimnetic water releases on the Flathead River (FR, 0.07 mg 1^–1). Annual mean concentrations of DOC were similar below both dams (1.62 mg 1^–1 FR; 1.71 KR). The percentage of POC in four size fractions differed in regulated and unregulated reaches of each river system; the smallest size fraction (0.45–10 smm) constituted a larger percentage of the total POC at the stations below the dams (50–93%), because POC in large size classes had settled out in the reservoir. The three largest size fractions (10–1000 µm) comprised a larger percentage of the total POC when samples were taken during conditions of full discharge from the dam. We measured large increases in all size classes of POC in samples collected during increasing discharges in a regulated reach, reflecting the component of sloughed periphyton and resuspended organic matter that were added during periods of hydropower generation at the dam. Seston (355 µm to 1 cm) collected in nets increased dramatically during increasing flows; concentrations of particulate organic matter (POM) in samples collected two and three hours after water levels began to rise were 572 and 1440 times higher than those collected during minimum discharge at the dam.     

土壤有机质概念和分组技术研究进展

土壤有机质一直是土壤学研究领域的重点,在过去的50年里,对土壤质量可持续性观念的增强和寻找快速判断人为因素对土壤质量影响方向指标的强烈愿望导致了土壤有机质的研究重点发生了急剧变化：对农业措施反映慢的土壤腐殖质类物质的研究正在退出土壤有机质研究领域,而侧重点逐渐转向了土壤中未受微生物作用或正在受微生物降解的有机残体;也出现了新的土壤有机质研究概念和对应测试手段：土壤有机质的比重分组、与有机质结合的土壤颗粒大小分组、土壤团聚体中的POM和iPOM以及土壤水溶性有机质和微生物体C等概念和测试手段被相继提了出来,土壤有机质的研究重点正在从土壤微生物的作用产物(腐殖质)向土壤微生物作用前的、具有部分生物活性的有机质(轻组有机质、砂粒组和粗粉砂粒组中的有机质、POM和iPOM)和完全具有生物活性的有机质(微生物体C和水溶性有机质)转移,这一过程与土壤有机质概念的拓展密不可分。     

Organic matter transport in an Appalachian Mountain river in Virginia,U.S.A.

Organic material transport in the New River, Virginia, was investigated over a 12 month period. Collections were made using drift nets and grab water samples from bridges at two sites about 210 km apart. About midway between the two sampling sites is a 1920 ha impoundment used for flood control and power generation. Dissolved organic matter (DOM) ranged 1–50 mg l^–1 at Site 1, upstream from the impoundment, and 11–19 mg l^–1 at Site 2 and was the most abundant form of organic matter at both sites during most periods of the year. Fine particulate organic matter (FPOM) ranged 1–45 mg l^–1 at Site 1 and 1–9 mg l^–1 at Site 2. Concentration of coarse particulate organic matter (CPOM) ranged 0.1–0.7 mg l^–1 at Site 1 and 0.1–0.2 mg l^–1 at Site 2. On an annual basis, the organic matter loads at Site 1 and Site 2 were computed to be 67 000 and 76 800 T y^–1, respectively, suggesting that the impoundment trapped and processed POM, and that municipal and industrial treatment facilities between the study sites supplemented DOM in the river.     

Plasmonic Back Reflectors: A Small Molecule Non‐fullerene Electron Acceptor for Organic Solar Cells

Organic bulk heterojunction photovoltaic devices predominantly use the fullerene derivatives [C60]PCBM and [C70]PCBM as the electron accepting component. This report presents a new organic electron accepting small molecule 2‐[{7‐(9,9‐di‐n‐propyl‐9H‐fluoren‐2‐yl)benzo[c][1,2,5]thiadiazol‐4‐yl}methylene]malononitrile (K12) for organic solar cell applications. It can be processed by evaporation under vacuum or by solution processing to give amorphous thin films and can be annealed at a modest temperature to give films with much greater order and enhanced charge transport properties. The molecule can efficiently quench the photoluminescence of the donor polymer poly(3‐n‐hexylthiophene‐2,5‐diyl) (P3HT) and time resolved microwave conductivity measurements show that mobile charges are generated indicating that a truly charge separated state is formed. The power conversion efficiencies of the photovoltaic devices are found to depend strongly on the acceptor packing. Optimized K12:P3HT bulk heterojunction devices have efficiencies of 0.73±0.01% under AM1.5G simulated sunlight. The efficiencies of the devices are limited by the level of crystallinity and nanoscale morphology that was achievable in the blend with P3HT.     

A Small Molecule Non‐fullerene Electron Acceptor for Organic Solar Cells

Organic bulk heterojunction photovoltaic devices predominantly use the fullerene derivatives [C60]PCBM and [C70]PCBM as the electron accepting component. This report presents a new organic electron accepting small molecule 2‐[{7‐(9,9‐di‐n‐propyl‐9H‐fluoren‐2‐yl)benzo[c][1,2,5]thiadiazol‐4‐yl}methylene]malononitrile (K12) for organic solar cell applications. It can be processed by evaporation under vacuum or by solution processing to give amorphous thin films and can be annealed at a modest temperature to give films with much greater order and enhanced charge transport properties. The molecule can efficiently quench the photoluminescence of the donor polymer poly(3‐n‐hexylthiophene‐2,5‐diyl) (P3HT) and time resolved microwave conductivity measurements show that mobile charges are generated indicating that a truly charge separated state is formed. The power conversion efficiencies of the photovoltaic devices are found to depend strongly on the acceptor packing. Optimized K12:P3HT bulk heterojunction devices have efficiencies of 0.73±0.01% under AM1.5G simulated sunlight. The efficiencies of the devices are limited by the level of crystallinity and nanoscale morphology that was achievable in the blend with P3HT.     

有机肥中可溶性有机碳、氮含量及其特性

测定了7种不同种类、不同腐熟程度有机肥中可溶性有机氮（SON）和可溶性有机碳（SOC）的含量,结果表明：有机肥的水和0．01mol／LCaCl2溶液提取液中SON含量分别平均为105．2mg／L和91．6mg／L;每千克干样平均含SON分别为1188mg和1037mg;SON占可溶性总氮（TSN）和全氮（TN）的比例分别在70．5％～74．7％和4．3％～4．9％之间。水和0．01mol／LCaCl2溶液提取液中SOC含量分别平均为695mg／L和622mg／L;每千克干样平均含SOC分别为7873mg和7054mg;SOC占有机肥有机碳（TOC）比例分别平均为2．1％和1．9％;SOC／SON平均分别为6．7和6．9。SON与SOC间的相关性较高,SON与NO3^--N含量呈现负相关关系。有机肥料中的可溶性氮素绝大部分以SON形式存在,如此高的SON和SOC含量可能会成为氮、碳养分流失和环境污染的潜在来源。     

落叶松林土壤溶液吸光度与土壤碳、氮含量的相关性

通过4个土壤深度100个样品14个波长(250、254、260、265、272、280、285、300、340、350、365、400、436和465 nm)土壤溶液吸光度值和土壤碳(可溶性碳DOC、全碳SOC)、土壤氮(可溶性氮DON、全氮SON)的测定,旨在探讨土壤溶液吸光度指示土壤碳氮指标的可行性及土壤深度对其可能影响。结论如下:(1)表层土壤和深层土壤吸光度值均随波长增加而指数下降,但表层土壤吸光度值较高,下降速度较快,较低波长更有利于区分表层和深层土壤溶液吸光度差异;和深层土壤相比,表层0～20 cm土壤SOC、DON和SON与不同波长吸光度有更好的相关性,但DOC与不同波长吸光度的相关性表层和深层差异较小;(2)250～300 nm的8个吸光度值具有高度相关性,它们在分析土壤溶液吸光度变化时具有等效性;基于所有数据的拟合分析发现,低波长(如254 nm)吸光度与土壤SOC、DON和SON相关性最高(R2=0.53～0.59),而更高波长(340 nm及以上)相关性明显降低。但DOC与254、340、365和400 nm吸光度相关性相差不大(R2=0.25～0.33)。这些发现说明,土壤溶液吸光度值,特别是低波长(250～300 nm)可以表征落叶松林土壤碳、氮相关指标的变化,但是需要考虑不同碳氮指标以及不同土层之间的差异。     

Seasonal Variability of Particulate Organic Matter in a Mountain Stream in Central Spain

The aim of this paper was to study the influence of environmental characteristics of the Mediterranean climate on seasonal variability of particulate organic matter abundance in a mountain stream. Coarse and fine fractions of both suspended and benthic particulate organic matter were determined on 14 occasions between February 1998 and November 1999 in a second‐order Mediterranean stream in Central Spain (Arroyo Mediano). Temporal variability of suspended organic matter followed a seasonal pattern, attributed to litter‐fall inputs, instream processing, and the hydrological regime. Suspended organic matter (SOM) and its seasonal variability fall well within the range reported for streams in temperate non‐Mediterranean deciduous forest. However, we found no seasonal trend in benthic organic matter (BOM) storage, and it seems that the amount of BOM remained fairly constant throughout the year. Reach retention (evaluated as the ratio between BOM and SOM per m²) was higher in summer during reduced stream flow, mainly due to coarse particulate organic matter storage. These observations do not differ from those reported for other headwater streams in temperate forested biomes, from which we conclude that there was no evidence of a Mediterranean influence on particulate organic matter dynamics in the Mediano stream, nor probably in other headwater Mediterranean streams. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Redox‐Active Organic Compounds for Future Sustainable Energy Storage System

Utilizing redox‐active organic compounds for future energy storage system (ESS) has attracted great attention owing to potential cost efficiency and environmental sustainability. Beyond enriching the pool of organic electrode materials with molecular tailoring, recent scientific efforts demonstrate the innovations in various cell chemistries and configurations. Herein, recent major strategies to build better organic batteries, are highlighted: diversifying charge‐carrying ions, modifying electrolytes, and utilizing liquid‐type organic electrodes. Each approach is summarized along with their advantages over Li‐ion batteries (LIBs). An outlook is also provided on the practical realization of organic battery systems, which hints at possible solutions for future sustainable ESSs.     

不同施肥处理对土壤活性有机碳和甲烷排放的影响

通过采集田间试验区连续3a施入有机肥的稻田耕层土壤,分析土壤中微生物量碳(MBC)、水溶性有机碳(DOC)、易氧化有机碳(ROC)和可矿化有机碳(readily mineralizable carbon,RMC)等活性有机碳的含量,稻田甲烷(CH_4)的排放通量,探讨施用有机肥的土壤活性有机碳变化及与CH_4排放的关系。研究结果显示:(1)施有机肥对土壤中的活性有机碳均有一定的促进作用。3a不同施肥处理土壤中DOC、ROC、MBC和RMC的平均含量分别为383.6、2501.2、640.4 mg/kg和291.7 mg/kg。3a施猪粪(猪粪+化肥,PM)、鸡粪(鸡粪+化肥,CM)和稻草(稻草+化肥,RS)的DOC的含量分别比化肥(CF)处理增加5.6%、6.7%和19.3%,ROC的含量分别比CF增加6.6%、8.4%和9.8%;MBC含量分别比CF增加5.1%、14.8%和21.5%,RMC增加6.8%、22.0%和33.9%。不同施肥处理的稻田土壤活性有机碳为分蘖期高于成熟期。(2)施肥处理显著增加稻田CH_4排放,CH_4分蘖期的排放通量是成熟期的143倍,3a PM、CM和RS处理的CH_4排放分别比CF处理增加37.0%(P0.05)、92.7%(P0.05)和99.4%(P0.05)。(3)不同施肥处理的DOC、ROC、MBC和RMC含量与CH_4排放通量均存在显著正相关关系,ROC与CH_4排放的相关系数最高,为0.754(P0.01),且4种有机碳间关系密切。稻田分蘖期土壤中的活性有机碳与稻田CH_4排放呈显著正相关关系。(4)综合分析,在4种有机碳中,土壤中ROC和MBC的含量直接影响CH_4排放。     

Chemical Characteristics and Origin of Dissolved Organic Matter in the Yukon River

Monthly (or bi-weekly) water samples were collected from the Yukon River, one of the largest rivers in North America, at a station near the US Geological Survey Stevens Village hydrological station, Alaska from May to September 2002, to examine the quantity and quality of dissolved organic matter (DOM) and its seasonal variations. DOM was further size fractionated into high molecular weight (HMW or colloidal, 1 kDa–0.45 μm) and low molecular weight (LMW, <1 kDa) fractions. Dissolved organic carbon (DOC), colored dissolved organic matter (C-DOM) and total dissolved carbohydrate (TCHO) species were measured in the size fractionated DOM samples. Concentrations of DOC were as high as 2830 μmol-C l⁻¹ during the spring breakup in May and decreased significantly to 508–558 μmol-C l⁻¹ during open-water season (June–September). Within the DOC pool, up to 85% was in the colloidal fraction (1 kDa–0.45 μm) in early May. As DOC concentration decreased, this colloidal portion remained high (70–85% of the bulk DOC) throughout the sampling season. Concentrations of TCHO, including monosaccharides (MCHO) and polysaccharides (PCHO), varied from 722 μmol-C l⁻¹ in May to 129 μmol-C l⁻¹ in September, which comprised a fairly constant portion of bulk DOC (24±2%). Within the TCHO pool, the MCHO/TCHO ratio consistently increased from May to September. The C-DOM/DOM ratio and the size fractionated DOM increased from May to September, indicating that DOM draining into the Yukon River contained increased amounts of humified materials, likely related to a greater soil leaching efficiency in summer. The average composition of DOM was 76% pedogenic humic matter and 24% aquagenic CHO. Characteristics of soil-derived humic substances and low chlorophyll-a concentrations support a dominance of terrestrial DOM in Yukon River waters.     

土壤非保护性有机碳对荒漠草原沙漠化的响应

沙化草地的恢复与重建是干旱半干旱区生态建设的重要内容,分析荒漠草原沙漠化过程中土壤非保护性有机碳分配比例的变异规律对于探讨沙化草地恢复机制具有重要的理论价值。以干旱、半干旱地区荒漠草原不同沙化阶段的土壤为研究对象,分析土壤粗颗粒有机碳、细颗粒有机碳、轻组有机碳含量和分配比例的分布特征、土壤非保护性有机碳转化为保护性有机碳的速率。结果表明:荒漠草原发生逆向演替后,土壤细颗粒有碳含量和分配比例表现为固定沙地荒漠草地半固定沙地流动沙地;粗颗粒有机碳含量表现为荒漠草地半固定沙地流动沙地固定沙地,粗颗粒有机碳分配比例表现为流动沙地半固定沙地荒漠草地固定沙地;轻组有机碳含量和分配比例递减。颗粒有机碳、轻组有机碳、土壤有机碳对草地沙漠化的敏感性不同,颗粒有机碳较轻组有机碳和土壤有机碳敏感性强,其中细颗粒有机碳较粗颗粒有机碳敏感性强。随着草地沙漠化程度的增强土壤非保护性有机碳分配比例呈下降趋势,表明草地沙漠化降低土壤质量。荒漠草地退化至流动沙地土壤非保护性有机碳转化为保护性有机碳的速率整体呈上升趋势。     

垦殖对新疆绿洲农田土壤有机碳组分及团聚体稳定性的影响

土壤有机碳是土壤质量变化的重要指标,土壤活性有机碳组分在土壤质量变化方面发挥重要作用。采用有机碳分组技术,研究了干旱荒漠区自然土壤开垦对绿洲农田土壤有机碳活性组分及团聚体稳定性的影响。结果表明:低有机碳含量的自然土壤垦殖后,有利于干旱荒漠区绿洲棉田土壤有机碳的积累,且垦殖(0-5a)增加显著,年均增加在0.65gkg-1以上,上升幅度为76%-286%,5a后维持在相对平衡的水平;土壤活性有机碳、轻组有机碳在垦殖0-5a显著增加,平均增加72%和99%,5a后下降;颗粒有机碳则表现出垦殖0-10a明显增加,增加在275%以上,10a后下降;土壤水稳性团聚体含量随垦殖年限的延长显著增加,0-20a内较自然土壤提高了75%。垦殖可能是干旱区绿洲农田潜在碳汇的重要影响因素;但随垦殖年限延长,土壤有机碳活性组分下降,土壤质量又存在一定的退化风险。     

Chromatographic techniques for the separation of Al and associated organic ligands present in soil solution

Organic acids including humic, fulvic, aliphatic and aromatic acids comprise part of the dissolved organic carbon (DOC) present in soil solution. They act as ligands for trace metals and are effective detoxifiers of monomeric aluminium (Al). Solid phase extraction (SPE) techniques permit fractionation of the DOC into organic classes but yield no information on the pre-existing Al/organic acid complexes. Aliphatic and aromatic acids may be separated and determined by High Performance Liquid Chromatography (HPLC); however, the conditions used dissociate the organic acid Al complexes. Humic and fulvic acids are of a variable and ill-defined nature and only limited information exists regarding their binding of Al. This paper reports on fractionation studies of soil solutions, using both SPE and molecular weight cut-off filters, to characterise the DOC components and on the subsequent development of a size exclusion chromatography (SEC) system for the separation of organically complexed Al into different species using a low ionic strength mobile phase at pH 4.2. Model complexes of Al and Cu citrate were used to evaluate chromatographic performance of a Fractogel TSK HW-40(S) column (1×30 cm). For soil solution samples, the column eluate, after passing through a UV detector, was directly coupled to an Inductively Coupled Plasma Atomic Emission Spectrometer (ICPAES) for on-line multi-element detection to characterise DOC and trace metal distribution.Fractionation studies revealed that polysaccharides constituted the major proportion of the DOC which passed the 10000 dalton molecular weight cut-off filter. Analysis of soil solutions from an organically amended soil by the SEC-ICPAES system showed that Al, Fe and Mn eluted as multiple peaks prior to the bed volume, indicating their presence as complexes with organic ligands.     

In Situ Morphology Studies of the Mechanism for Solution Additive Effects on the Formation of Bulk Heterojunction Films

The most successful active film morphology in organic photovoltaics is the bulk heterojunction (BHJ). The performance of a BHJ arises from a complex interplay of the spatial organization of the segregated donor and acceptor phases and the local order/quality of the respective phases. These critical morphological features develop dynamically during film formation, and it has become common practice to control them by the introduction of processing additives. Here, in situ grazing incidence X‐ray diffraction (GIXD) and grazing incidence small angle X‐ray scattering (GISAXS) studies of the development of order in BHJ films formed from the donor polymer poly(3‐hexylthiophene) and acceptor phenyl‐C61‐butyric acid methyl ester under the influence of two common additives, 1,8‐octanedithiol and 1‐chloronaphthalene, are reported. By comparing optical aggregation to crystallization and using GISAXS to determine the number and nature of phases present during drying, two common mechanisms by which the additives increase P3HT crystallinity are identified. Additives accelerate the appearance of pre‐crystalline nuclei by controlling solvent quality and allow for extended crystal growth by delaying the onset of PCBM‐induced vitrification. The glass transition effects vary system‐to‐system and may be correlated to the number and composition of phases present during drying.     

颗粒有机质的来源、测定及其影响因素

土壤活性有机质及其组分作为土壤质量的重要指标在土壤化学、物理和生物性质方面起着重要作用。颗粒有机质能够有效地反映有机质的特性,与微生物生长、营养供给及C、N的生物学调节密切相关。作为活性有机质的一个量度指标,颗粒有机质越来越受到人们的重视。本文综述了土壤颗粒有机质的来源及其在土壤有机质转化过程中的作用,对其测定方法作了系统的描述,阐明了土壤理化性质、农业措施(施肥与耕作)及土地利用类型对土壤颗粒有机质在土壤形成及维持其稳定性方面的影响。