Peanut Straw Decomposition Products Promoted by Chemical Additives and Their Effect on Enzymatic Activity and Microbial Functional Diversity in Red Soil

ABSTRACT

The objectives of the present study were to determine the promotional effect of chemical additives on quality of peanut straw decomposition products and to evaluate the influence of the resulting products on soil biological properties. Straw was mixed with or without chemical additives, such as iron(II) sulfate (FeSO₄), alkali slag, or FeSO₄ combined with alkali slag, and decomposed for 50 days. The decomposition products were used as organic fertilizer and added to red soil for an incubation experiment. The chemical additives increased total organic carbon (C), total nitrogen (N), and available N content but decreased the C:N ratios in decomposition products compared to controls. Adding FeSO₄ gave the highest humic acid content (HA, 30.34 g kg^?1) and ratio of humic to fulvic acid (HA/FA, 0.53) and the lowest ratio of HA absorption value at 465 nm to that at 665 nm (E₄/E₆, 6.05), suggesting high humification of decomposition products. Application of the resulting products to soil increased soil urease and invertase activities. BIOLOG analysis showed that microbial C utilization ability, Shannon–Weaver diversity, and McIntosh evenness indexes were improved by the organic fertilizer promoted by chemical additives. Principal component analysis indicated that microbial community structures were also influenced by different amendments in decomposition products. Our study provides a reference point for acquiring high quality straw compost and improving soil biological functions by organic fertilizer.     

Temporal responses of soil biological characteristics to organic inputs and mineral fertilizers under wheat cultivation in inceptisol

A 2-year field experiment was conducted in wheat ecosystem to assess the key soil biological characteristics in inceptisols of northeastern region of India. Nine treatments using organic inputs (farmyard manure and vermicompost) and mineral fertilizers were applied by modulating the doses of organics and mineral N fertilizer. Soil enzymes (urease, phosphatase, dehydrogenase, fluorescein diacetate (FDA) and arylsulphatase), microbial biomass carbon (MBC), bacteria and fungi populations were measured before seed sowing (GS₁), at flowering stage (GS₂) and after harvest (GS₃) of wheat, whereas total organic carbon (TOC) was studied at GS₃. GS₂ recorded significantly higher soil enzyme activities, except FDA, which increased considerably at GS₃. Enzyme activities, available N and TOC significantly (p ≤ 0.05) enhanced with application of organic inputs even with reduced (50%) mineral N. Except urease and phosphatase, other enzymes did not respond significantly to mineral fertilization. Vermicompost application increased mean enzyme activities, MBC, microbial growth and TOC fractions (particulate organic carbon, humic acid and fulvic acid carbon) than farmyard manure. Significant (p ≤ 0.05) positive correlations (r = 0.61–0.87) were obtained between TOC and its fractions with studied soil enzymes. Thus, in conclusion, 5 t ha^–1 organics incorporation (especially vermicompost) in wheat fertility programme can uphold soil biological health, reduce (50%) N application and would be a sustainable option for wheat grown in inceptisols of northeastern region of India.     

Relationship between molecular characteristics of soil humic fractions and glycolytic pathway and krebs cycle in maize seedlings

A humic acid (HA) isolated from a volcanic soil was separated in three fractions of decreasing molecular size (I, II and III) by preparative high performance size exclusion chromatography (HPSEC). The molecular content of the bulk soil HA and its size fractions was characterized by pyrolysis-GC-MS (thermochemolysis with tetramethylammonium hydroxide) and NMR spectroscopy. All soil humic materials were used to evaluate their effects on the enzymatic activities involved in glycolytic and respiratory processes of Zea mays (L.) seedlings. The elementary analyses and NMR spectra of the humic fractions indicated that the content of polar carbons (mainly carbohydrates) increased with decreasing molecular size of separated fractions. The products evolved by on-line thermochemolysis showed that the smallest size fraction (Fraction III) with the least rigid molecular conformation among the humic samples had the lowest content of lignin moieties and the largest amount of other non-lignin aromatic compounds. The bulk HA and the three humic fractions affected the enzyme activities related to glycolysis and tricarboxylic acid cycle (TCA) in different ways depending on molecular size, molecular characteristics and concentrations. The overall effectiveness of the four fractions in promoting the metabolic pathways was in the order: III>HA>II>I. The largest effect of Fraction III, either alone or incorporated into the bulk HA, was attributed to a flexible conformational structure that promoted a more efficient diffusion of bioactive humic components to maize cells. A better knowledge of the relationship between molecular structure of soil humic matter and plant activity may be of practical interest in increasing carbon fixation in plants and redirect atmospheric CO₂ into bio-fuel resources.     

Long-Term Effect of Fertilizers and Amendments on Different Fractions of Organic Matter in an Acid Alfisol

The effect of fertilizers and amendments on organic matter dynamics in an acid Alfisol was studied in a long-term field experiment initiated during 1972 at experimental farm of Department of Soil Science, CSK HPKV, Palampur (India). Continuous application of chemical fertilizers either alone or in combination with farmyard manure (FYM) or lime for 42 years significantly influenced water-soluble organic carbon (WS-OC), water-soluble carbohydrate (WS-CHO), soil microbial biomass carbon, soil microbial biomass nitrogen, soil microbial biomass phosphorus, soil microbial biomass sulfur, humic acid (HA), and fulvic acid (FA). Continuous cropping without fertilization resulted in depletion to the order of 17, 21, 24, 23, 22, 26, 12, and 18% in WS-OC, WS-CHO, microbial biomass carbon, microbial biomass nitrogen, microbial biomass phosphorus, microbial biomass sulfur, HA, and FA, respectively. Different fractions of soil organic matter were found to be positively and significantly correlated with grain and straw/stover yield of wheat and maize crops.     

Fate of humic acids isolated from natural humic substances

Composition of humic acids (HA) is a function of plant-derived inputs, degradation processes regulated by microorganisms, organo-mineral interactions and age. Characterization of different origin humic substances is important for evaluation of their contribution to stabile and labile carbon pool in the environment. The relative abundance of chemical components in HA isolated from soils, compost, commercial lignohumates, alginite, acadiane and lignite was studied with aim to quantify content of important biomarkers such as amino acid, lipids and polyphenols. HA were considered as a heterogeneous complex and high concentration of peptides, polyphenols and lipids was determined in acadian-HA to compare with soil-HA. Compost-HA contained much more amino acids to compare with soil-HA samples. Alginite-HA and lignite-HA were similar in biomarkers content to soil-HA. Fourier transform infrared spectroscopy confirmed that chemical composition and functional groups content differs with the origin, humification degree and the age of studied samples. Soil-HA are typically composed of a variety of ?OH, COOH?, C–O, C–H₂, (aliphatic and aromatic) groups, quinines, lignin fragments, polysaccharide, monosaccharide and proteins fragments, which are linked together by ?O?, ?NH?, ?H=, >C=O, metal ions and –S? groups. ¹³C NMR spectroscopy showed that aromatic carbon content was the highest in lignite-HA and soil-HA.     

Composition of organic C fractions in soils of different texture affected by sugarcane monoculture

ABSTRACT

Sugarcane is a strategic commodity in Indonesia. It is usually raised in a monoculture system. There is a lack of information about the effects of extended sugarcane monoculture on the soil carbon fraction. The aim of this study was to determine the relative changes in the soil organic C fractions in response to the duration of sugarcane monoculture on Entisols, Inceptisols, and Vertisols. The measured variables were the percentages of sand, silt, and clay, organic matter (OM), total nitrogen (TN), pH (H₂O), cation exchange capacity (CEC), NH₄ ⁺, NO₃ ^-, labile carbon fraction (soil carbon mineralization (C-Min), soil microbial carbon (C-Mic), and carbon particulate organic matter (C-POM)), and stable carbon fraction (humic and fulvic acids). Soil type with sugarcane monoculture period had significant influences on the percentages of clay, sand, silt, CEC, and pH (H₂O). Soil type and sugarcane monoculture period had no apparent significant effect on C-Min or C-POM but did significantly influence C-Mic. The humic and fulvic acid levels in all three soil types were affected by the duration of sugarcane monoculture. To establish the impact of long-term sugarcane monoculture on the physicochemical properties of soils with various textures, it is more appropriate to measure the soil stable carbon fractions such as humic and fulvic acid rather than the soil labile carbon fractions such as C-Min, C-POM, or C-Mic.     

不同施肥条件土壤胡敏酸级分变异及性质的研究

以１７年长期定位试验土壤为材料,在研究土壤有机质氧化稳定性基础上,采用酒精沉淀分级方法,对不同施肥处理土壤胡敏酸的级分及光学性质进行了研究,并对胡敏酸及其级分的类型进行了划分。结果表明长期施用有机（堆肥及秸秆）土壤有机质含量明显增加,有机质的氧化稳定系数降低,土壤胡敏酸组成分布中心向高浓度酒精析出的级分偏移,颗粒小的级分比例增大,土壤胡敏酸的Ｅ４,Ｅ６值减小Ｅ４／Ｅ６增大,而单施化肥则有相反趋势。     

THE ACCUMULATION OF SOIL ORGANIC MATTER AND ITS CARBON ISOTOPE CONTENT IN A CHRONOSEQUENCE OF SOILS DEVELOPED ON AEOLIAN SAND IN NEW ZEALAND

Soil organic matter was extracted by a mixture of O.IM Na₄P₂O: O.IM NaOH from a chronosequence of weakly weathered soils developed on aeolian sand, and fractionated into humin (non-extractable), humic acid, and fulvic acid. The mass of total organic carbon in the profiles, the ¹⁴C content and the ¹³C/12C ratios were also determined. The weight of total carbon increased rapidly at first and then gradually without attaining a steady state. This trend was also shown by the humin and fulvic acid fractions, but the humic acid fraction appeared to have reached a maximum after about 3000 years. The order of total weights of the organic fractions was humin > fulvic acid > humic acid. The evidence suggests that the proportions of the humic fractions formed by decomposition are related to soil differences but not to vegetation. The greater part of the plant material found in the soils appears in the humin and fulvic acid fractions.     

The fate of catechol in soil as affected by earthworms and clay

The effect of endogeic earthworms (Octolasion tyrtaeum) and the availability of clay (Montmorillonite) on the mobilization and stabilization of uniformly ¹⁴C-labelled catechol mixed into arable and forest soil was investigated in a short- and a long-term microcosm experiment. By using arable and forest soil the effect of earthworms and clay in soils differing in the saturation of the mineral matrix with organic matter was investigated. In the short-term experiment microcosms were destructively sampled when the soil had been transformed into casts. In the long-term experiment earthworm casts produced during 7 days and non-processed soil were incubated for three further months. Production of CO₂ and ¹⁴CO₂ were measured at regular intervals. Accumulation of ¹⁴C in humic fractions (DOM, fulvic acids, humic acids and humin) of the casts and the non-processed soil and incorporation of ¹⁴C into earthworm tissue were determined.Incorporation of ¹⁴C into earthworm tissue was low, with 0.1 and 0.44% recovered in the short- and long-term experiment, respectively, suggesting that endogeic earthworms preferentially assimilate non-phenolic soil carbon. Cumulative production of CO₂-C was significantly increased in casts produced from the arable soil, but lower in casts produced from the forest soil; generally, the production of CO₂-C was higher in forest than in arable soil. Both soils differed in the pattern of ¹⁴CO₂-C production; initially it was higher in the forest soil than in the arable soil, whereas later the opposite was true. Octolasion tyrtaeum did not affect ¹⁴CO₂-C production in the forest soil, but increased it in the arable soil early in the experiment; clay counteracted this effect. Clay and O. tyrtaeum did not affect integration of ¹⁴C into humic fractions of the forest soil. In contrast, in the arable soil O. tyrtaeum increased the amount of ¹⁴C in the labile fractions, whereas clay increased it in the humin fraction.The results indicate that endogeic earthworms increase microbial activity and thus mineralization of phenolic compounds, whereas clay decreases it presumably by binding phenolic compounds to clay particles when passing through the earthworm gut. Endogeic earthworms and clay are only of minor importance for the fate of catechol in soils with high organic matter, clay and microbial biomass concentrations, but in contrast affect the fate of phenolic compounds in low clay soils.     

Transformation of organic matter from maize residues into labile and humic fractions of three European soils as revealed by 13C distribution and CPMAS-NMR spectra

The dynamics of incorporation of fresh organic residues into the various fractions of soil organic matter have yet to be clarified in terms of chemical structures and mechanisms involved. We studied by ¹³C‐dilution analysis and CPMAS‐¹³C‐NMR spectroscopy the distribution of organic carbon from mixed or mulched maize residues into specific defined fractions such as carbohydrates and humic fractions isolated by selective extractants in a year‐long incubation of three European soils. The contents of carbohydrates in soil particle size fractions and relative δ¹³C values showed no retention of carbohydrates from maize but rather decomposition of those from native organic matter in the soil. By contrast, CPMAS‐¹³C‐NMR spectra of humic (HA) and fulvic acids (FA) extracted by alkaline solution generally indicated the transfer of maize C (mostly carbohydrates and peptides) into humic materials, whereas spectra of organic matter extracted with an acetone solution (HE) indicated solubilization of an aliphatic‐rich, hydrophobic fraction that seemed not to contain any C from maize. The abundance of ¹³C showed that all humic fractions behaved as a sink for C from maize residues but the FA fraction was related to the turnover of fresh organic matter more than the HA. Removal of hydrophobic components from incubated soils by acetone solution allowed a subsequent extraction of HA and, especially, FA still containing much C from maize. The combination of isotopic measurements and NMR spectra indicated that while hydrophilic compounds from maize were retained in HA and FA, hydrophobic components in the HE fraction had chemical features similar to those of humin. Our results show that the organic compounds released in soils by mineralization of fresh plant residues are stored mainly in the hydrophilic fraction of humic substances which are, in turn, stabilized against microbial degradation by the most hydrophobic humic matter. Our findings suggest that native soil humic substances contribute to the accumulation of new organic matter in soils.     

间伐对杉木人工林土壤碳氮及其组分特征的影响

为探究不同间伐强度对杉木人工林土壤碳氮及其组分特征的影响,以福建省三明市官庄国有林场11年生杉木(Cunninghamia lanceolata)人工林为研究对象,采用弱度间伐(LIT)、中度间伐(MIT)、强度间伐(HIT)等3种间伐强度,研究不同间伐强度林分0—10,10—20,20—40,40—60,60—80,80—100 cm土层总有机碳(SOC)、全氮(TN)及易氧化有机碳(ROC)、硝态氮(NO_3~--N)、铵态氮(NH_4~+-N)、微生物量碳(MBC)、微生物量氮(MBN)、微生物熵碳(qMBC)、微生物熵氮(qMBN)的变化特征,以探讨不同间伐强度对杉木人工林土壤碳氮及其组分特征的影响。结果表明:间伐降低了土壤SOC和TN的含量,降低幅度分别为1.4%～36.9%,3.1%～45.7%。间伐增加了土壤MBC、NO_3~--N的含量,而对ROC、NH_4~+-N和MBN的程度在不同土层有差异,qMBC和qMBN随着间伐强度的增加而增大。相关性分析表明,土壤SOC分别与TN、qMBC、ROC、NH_4~+-N、MBC、MBN呈极显著正相关(P0.01);TN与qMBN、ROC、NH_4~+-N、MBC、MBN呈极显著正相关(P0.01)。杉木人工林间伐处理降低了土壤表层SOC和TN含量,增加了土壤SMBC和qMBC、qMBN,同时也增加了土壤表层(0—10 cm)SMBN。抚育间伐导致土壤SOC和TN含量降低主要是由于活性碳、氮含量的增加,提高土壤中有机质分解速率,最终导致土壤SOC和TN含量降低。     

红松人工林腐殖质组成及其结合形态研究

 运用野外调查与实验分析相结合的方法,对不同生长发育阶段红松人工林（林龄25、45、58、68 a）和红松混交林（林龄60a）根际与非根际土壤有机质含碳量、腐殖质组成与结合形态进行了研究。结果表明:不同年龄阶段红松人工纯林、红松混交林土壤有机质含碳量、腐殖质各组分含碳量随土层深度的加深而降低,并且根际土壤高于非根际土壤。就土壤腐殖质组成而言,除林龄58a红松人工林根际土壤和45a红松人工林非根际土壤外,其他林型土壤胡敏酸含碳量均高于富里酸含碳量;胡敏酸与富里酸比值（HA/FA）在1.00～2.45之间;土壤重组腐殖质、松结态腐殖质、稳结态腐殖质含碳量大小顺序为林龄58>68>25>45a;红松混交林除紧结态腐殖质外,其他腐殖质各组分含碳量均高于红松人工林。     

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.     

长期施肥对小麦-玉米作物系统土壤腐殖质组分碳和氮的影响

通过对华北平原小麦–玉米轮作农田生态系统18年田间施肥试验,研究了长期不同施肥处理对耕层（0—20 cm）土壤腐殖质及活性腐殖质组分碳和氮的影响。试验设化肥NPK不同组合（NPK、NP、NK、PK）,全部施用有机肥（OM）,一半有机肥+化肥NPK（1/2OMN）及不施肥（CK）共7个处理。结果表明,各施肥处理均能在不同程度上增加土壤腐殖质（胡敏酸、富里酸和胡敏素）及活性腐殖质（活性胡敏酸和活性富里酸）组分碳和氮含量,提高可浸提腐殖质（胡敏酸和富里酸）及活性腐殖质组分碳和氮分配比例;但施肥对土壤活性腐殖质组分碳和氮含量的增加率均分别高于腐殖质组分碳和氮。各处理土壤腐殖质及活性腐殖质组分碳和氮含量均为OM处理最高,且有机肥与化肥NPK配施高于单施化肥各处理;而化肥处理中NPK均衡施用效果最好。说明施用有机肥、有机肥与化肥NPK配施及化肥NPK均衡施用是增加土壤腐殖质及活性腐殖质组分碳和氮的关键;活性腐殖质组分碳和氮较腐殖质组分碳和氮对施肥措施的响应更灵敏。     

Characterization of organic matter fractions in the top layer of soils under different land uses in Central‐Eastern Europe

The objective of this study was to investigate differences in organic matter fractions, such as dissolved organic carbon and humic substances, in soils under different land uses. Soil samples were collected from the upper layer of arable lands and grasslands. Humic substances (HS) were chemically fractionated into fulvic acids (FA), humic acids (HA) and humins (HUM), and based on the separated fractions, the humification index (HI) and the degree of HS transformation (DT) were calculated. Dissolved organic carbon (DOC) was determined by cold (CWE) and hot water (HWE) extractions. Regardless of land use, the results indicated significant differences in soil organic carbon (SOC) and HS composition, with HA and HUM as the dominant fractions. Total SOC was higher in grassland (median = 17.51 g kg^?1) than arable soils (median = 9.98 g kg^?1); the HI and DT indices did not differ significantly between land uses (HI = 0.3–10.3 and DT = 0.2–6.2 for grasslands, p > 0.05; HI = 0.3–3.9 and DT = 0.2–20.1 for arable lands, p > 0.05). This indicates the relatively high stability of organic carbon and efficient humification processes in both land uses. Additionally, in arable soils lower CWE‐C (0.75 g kg^?1) and higher HWE‐C (2.59 g kg^?1) than in grasslands (CWE‐C = 1.13 g kg^?1, HWE‐C = 1.60 g kg^?1) can be related to farming practice and application of soil amendments. The results showed that both labile and humified organic matter are better protected in grassland soils and are consequently less vulnerable to mineralization.     

Microbial use of lignite compared to recent plant litter as substrates in reclaimed coal mine soils

In the Lusatian mining district, rehabilitated mine soils contain substantial amounts of lignite in addition to recent carbon derived from plant litter. The aim of this study was to examine the importance of the two organic matter types as substrates for soil microbial biomass in mine soils containing organic matter with a contrasting degree of humification. Samples were taken from the lignite-containing overburden material, from a mine soil under 14-year-old black pine (Pinus nigra) and from a mine soil under 37-year-old red oak (Quercus rubra). Overburden material was ameliorated with alkaline ash and incubated in an identical manner as the 14-year-old and 37-year-old mine soils for 16 months. Carbon mineralisation was monitored throughout. After 0, 3, 6, 12 and 16 months, samples were removed and analysed for chemical parameters and for microbial biomass. In addition, ¹⁴C activity measurements in bulk soil and microbial biomass were used to estimate their lignite content.Despite the high content of organic carbon in lignite-rich overburden material, low contents of microbial biomass were recorded. Ash-amelioration led to high pH values in the overburden material, resulting in high concentrations of dissolved organic carbon most likely derived from lignite. Development of the microbial community was subsequently stimulated by presence of an easily available carbon source. In older mine soils, larger amounts of microbial biomass are most likely related to the presence of recent organic matter. Radiocarbon analysis of the microbial biomass extracted from the 14-year-old mine soil indicated higher lignite carbon contribution than recorded for microbial biomass of the 37-year-old mine soil. The highest concentration of lignite C present in microbial biomass as indicated by the C_mic/C_org ratio was, however, observed in the ameliorated overburden material. Therefore, we conclude that the importance of lignite as a carbon source for micro-organisms decreases when recent organic matter is present in the older stages of mine soil development.     

Electron donors and acceptors influence anaerobic soil organic matter mineralization in tidal marshes

Anaerobic decomposition in wetland soils is carried out by several interacting microbial processes that influence carbon storage and greenhouse gas emissions. To understand the role of wetlands in the global carbon cycle, it is critical to understand how differences in both electron donor (i.e., organic carbon) and terminal electron acceptor (TEA) availability influence anaerobic mineralization of soil organic matter. In this study we manipulated electron donors and acceptors to examine how these factors influence total rates of carbon mineralization and the pathways of microbial respiration (e.g., sulfate reduction versus methanogenesis). Using a field-based reciprocal transplant of soils from brackish and freshwater tidal marshes, in conjunction with laboratory amendments of TEAs, we examined how rates of organic carbon mineralization changed when soils with different carbon contents were exposed to different TEAs. Total mineralization (the sum of CO₂ + CH₄ produced) on a per gram soil basis was greater in the brackish marsh soils, which had higher soil organic matter content; however, on a per gram carbon basis, mineralization was greater in the freshwater soils, suggesting that the quality of carbon inputs from the freshwater plants was higher. Overall anaerobic metabolism was higher for both soil types incubated at the brackish site where SO₄²⁻ was the dominant TEA. When soils were amended with TEAs in the laboratory, more thermodynamically favorable respiration pathways typically resulted in greater organic matter mineralization (Fe(III) respiration > SO₄²⁻ reduction > methanogenesis). These results suggest that both electron donors and acceptors play important roles in regulating anaerobic microbial mineralization of soil organic matter.     

Organic matter in density fractions of water-stable aggregates in silty soils: Effect of land use

The location of soil organic matter (SOM) within the soil matrix is considered a major factor determining its turnover, but quantitative information about the effects of land cover and land use on the distribution of SOM at the soil aggregate level is rare. We analyzed the effect of land cover/land use (spruce forest, grassland, wheat and maize) on the distribution of free particulate organic matter (POM) with a density <1.6 g cm⁻³ (free POM_<1.6), occluded particulate organic matter with densities <1.6 g cm⁻³ (occluded POM_<1.6) and 1.6-2.0 g cm⁻³ (occluded POM_1.6-2.0) and mineral-associated SOM (>2.0 g cm⁻³) in size classes of slaking-resistant aggregates (53-250, 250-1000, 1000-2000, >2000 μm) and in the sieve fraction <53 μm from silty soils by applying a combined aggregate size and density fractionation procedure. We also determined the turnover time of soil organic carbon (SOC) fractions at the aggregate level in the soil of the maize site using the ¹³C/¹²C isotope ratio. SOM contents were higher in the grassland soil aggregates than in those of the arable soils mainly because of greater contents of mineral-associated SOM. The contribution of occluded POM to total SOC in the A horizon aggregates was greater in the spruce soil (23-44%) than in the grassland (11%) and arable soils (19%). The mass and carbon content of both the free and occluded POM fractions were greater in the forest soil than in the grassland and arable soils. In all soils, the C/N ratios of soil fractions within each aggregate size class decreased in the following order: free POM_<1.6>occluded POM_<1.6-2.0>mineral-associated SOM. The mean age of SOC associated with the <53 μm mineral fraction of water-stable aggregates in the Ap horizon of the maize site varied between 63 and 69 yr in aggregates >250 μm, 76 yr in the 53-250 μm aggregate class, and 102 yr in the sieve fraction <53 μm. The mean age of SOC in the occluded POM increased with decreasing aggregate size from 20 to 30 yr in aggregates >1000 μm to 66 yr in aggregates <53 μm. Free POM had the most rapid rates of C-turnover, with residence times ranging from 10 yr in the fraction >2000 μm to 42 yr in the fraction 53-250 μm. Results indicated that SOM in slaking-resistant aggregates was not a homogeneous pool, but consisted of size/density fractions exhibiting different composition and stability. The properties of these fractions were influenced by the aggregate size. Land cover/land use were important factors controlling the amount and composition of SOM fractions at the aggregate level.     

减氮配施有机物质对土壤氮素淋失的调控作用

采用室内土柱模拟试验方法,研究不同氮肥施用下1m土体中氮素的分布和移动特征,揭示土壤氮素动态变化规律。结果表明:FN(农民习惯施无机氮用量)、RN(根据土壤养分供应和作物需求确定的推荐无机氮用量)显著增加了土壤上层NH_4^+-N和NO_3^--N向下层淋失。RN+HA(与推荐无机氮纯养分相等的锌腐酸尿素)和RN40%+OMB(推荐无机氮肥减60%基础上配施自制有机调理物质)可延长上层土壤NH_4^+-N峰值出现时间,降低下层NH_4^+-N。淋溶结束后,等氮量下增施HA较RN降低60cm以下NH_4^+-N残留29.7%～54.2%;降低60—80cm NO_3^--N累积17.4%。RN40%+OMB处理无机氮肥用量最小,0—20cm的NH_4^+-N最高,40—100cm稳定在2.0mg/kg左右;0—20,20—40cm土层NO_3^--N较RN+HA增加12.3%和2.0%,显著降低40cm以下NO_3^--N残留。RN+HA和RN40%+OMB较RN的土壤总无机氮残留分别减少7.4%和20.2%,降低表观淋失率。因此,RN40%+OMB可较好地抑制氮素下移,降低氮素淋失风险,为减少氮素淋失、明确合理氮肥施用方式提供科学依据。     

Effect of organic-complexed superphosphates on microbial biomass and microbial activity of soil

Organic complexed super-phosphates (CSPs) are formed by the complexation of humic acid (HA) with calcium monophosphate. The aim of this study was to determine whether two CSPs, characterized by different HA concentrations, added to a calcareous soil at an agronomic dose, were able to maintain the phosphorus (P) in a soluble form longer than the superphosphate fertilizer. Another important goal was to verify if CSP could positively influence soil microbial biomass and soil microbiological activities. Organic complexed super-phosphates were capable of keeping a large portion of P in a soluble form under different soil water conditions. In particular, the CSP with the highest organic C content was the most effective product, capable of maintaining, in an available form, the 73 % of the initially added P at the end of the experiment. In addition, it was the most effective in increasing C–CO₂ soil emission, microbial biomass carbon (C) and nitrogen (N), fluoresceine diacetate hydrolysis and activities of alkaline phosphomonoesterase, β-glucosidase and urease. The addition of CSPs to soil probably produced a priming effect, increasing several times C–CO₂ release by the treated soil. The significant correlation (p?<?0.05) between C–CO₂ emission and the amount of C added to soil by CSP suggests that the added HA acted as trigger molecules.