Contrasting composition of free and mineral-bound organic matter in top- and subsoil horizons of Andosols

Andosols are characterised by high organic matter (OM) content throughout the soil profile, which is mainly due to the stabilisation of soil organic matter (SOM) by mineral interactions. The aim of the study was to examine whether there were differences in the chemical composition of mineral-associated SOM and free OM in the top A horizon and in the subsoil (horizons below the A11 horizon). Our experimental approach included the replicated sampling of a fulvic and an umbic Andosol under pine and laurel forest located on the island of Tenerife with a Mediterranean sub-humid climate. We determined the extent of the organo-mineral interactions by comparing the sizes of the light (free) and heavy (dense) soil fractions obtained by physical separation through flotation in a liquid with a density of 1.9 g cm^–3. We determined the elemental and isotopic composition of both fractions and analysed their chemical composition by analytical pyrolysis. The elemental and isotopic composition showed similar values with depth despite the different vegetation and climatic conditions prevailing at the two sites. Carbon (C) stabilised by mineral interactions increased with depth and represented 80–90% of the total C in the lowest horizons. The heavy fractions mainly released N-containing compounds upon analytical pyrolysis, whereas lignin-derived and alkyl compounds were the principal pyrolysis products released from the light fractions of the top- and subsoil horizons. Principal component analysis showed that the chemical composition of OM stabilised by mineral interaction differs in the different horizons of the soil profile. In the A horizons, the chemical composition of this OM was similar to those of the light fractions, i.e. litter input. There was a gradual change in the bulk molecular composition from a higher contribution of plant-derived molecules in the light and heavy fractions of the A horizon to more microbial-derived molecules as well as black C-derived molecules at depth. We conclude that transport processes in addition to decomposition and possibly in situ ageing affect the chemical composition of mineral-associated OM in subsoils.     

Stabilised carbon in subsoil horizons is located in spatially distinct parts of the soil profile

Soil organic matter (SOM) stabilisation in subsoil horizons received much attention in recent years, due to the presence of compounds with very long residence times. The reasons for enhanced organic carbon stabilisation in subsoil horizons are poorly understood. In this study, we characterised SOM in adjacent soil compartments with different pedological functioning. We sampled SOM in visually identifiable zones in form of tongues and the adjacent soil matrix from deep soil horizons (60-140 cm depth) of 3 profiles under agricultural land. The samples were analysed for elemental and isotopic composition, radiocarbon age, chemical composition and lignin signature. The objective of the study was to examine if the tongues are characterised by contrasting carbon amounts and composition with regards to the soil matrix.Our results indicate that tongues have two times higher carbon content and are depleted in ¹⁵N with regards to the adjacent soil matrix. SOM in the tongues is characterised by up to modern radiocarbon ages, whereas SOM in the adjacent soil matrix is several thousand years old. Twenty percent more HF soluble carbon in the soil matrix suggest that more mineral bound, highly mobile SOM is present compared to tongues. Differences in chemical composition concern the lignin component, which seems to be preserved in the soil matrix. These data may be explained by different functioning in the two parts of the soil profile. In tongues, fresh carbon input by preferential flow and/or roots may lead to higher SOM turnover compared to the soil matrix. This heterogeneous distribution of stabilised SOM must be taken into account, when studying carbon sequestration in deep soil horizons.     

Investigating the effects of wettability and pore size distribution on aggregate stability: the role of soil organic matter and the humic fraction

Soil organic matter (SOM) is an important factor influencing aggregate stability. Interactions between SOM and soil structure are widely studied, although the subtle relationship between SOM content, pore size distribution and aggregate stability is not fully known. Here we investigate such a relationship by means of a long‐term experiment established in 1962 in northeastern Italy, which considers different fertilizer practices (organic, mineral and mixed) applied to a continuous maize crop rotation. We measured wet stability of 1–2 mm aggregates subjected to different pretreatments. Both soil physical properties (such as pore size distribution and hydrophobicity) and chemical properties (soil organic and humic carbon content) affecting aggregate stability were considered. The chemical structure of humic substances was characterized by thermal and spectroscopic analyses (TG‐DTA, DRIFT and ¹H HR MAS NMR). The Pore‐Cor network model was then applied to evaluate the contribution of hydrophobicity and porosity to aggregate wetting. Our study suggests that SOM and its humic fraction can affect aggregate wetting and consequently slaking by modifying the pore size distribution with a shift from micropores (5–30 µm) and mesopores (30–75 µm) to ultramicropores (0.1–5 µm); hydrophobicity was also increased as a result of different humic composition. Spectroscopic analysis showed that hydrophobic compounds were mostly associated with complex humic molecules. Models of fast wetting dynamics, however, suggest that the contribution that hydrophobicity makes to aggregate stability, especially to soils with large carbon inputs, may not be the most significant factor.     

Particle-size distribution patterns in Vertisols and vertic soils of Russia

Five variants of the distribution of clay (<0.001 mm) and physical clay (<0.01 mm) fractions along the vertical profiles of Vertisols (slitozems) and vertic soils (slitic subtypes of different soil types) from the European part of Russia are distinguished: (1) accumulative, (2) even, (3) regressive, (4) with a maximum in the middle-profile horizon and with their approximately equal contents in the upper and the lower horizons, and (5) eluvial–illuvial. These distribution patterns are related to the lithological specificity of sedimentation and formation of parent materials composed of swelling clays of different geneses and ages. Solonetzic, eluvial- gley, and solodic processes contribute to the development of the eluvial–illuvial and, partly, regressive variants of clay distribution. All the five variants with a predominance of the even distribution pattern can be found in Vertisols. Most of Vertisols in the European part of Russia have a medium clayey or a heavy clayey texture in the entire profile. The regressive distribution pattern is typical of the group of vertic soils. In the upper horizons of Vertisols, where slickensides do not form, the texture is usually heavier than that in the analogous horizons of vertic soils. The middle-profile and lower horizons with slickensides have similar statistical distributions of particle-size fractions in Vertisols proper and in vertic soils. However, in Vertisols, a tendency for a more frequent occurrence of the soils with a higher content of the clay fraction and with a higher portion of this fraction in the physical clay fraction is observed (as compared with the vertic soils).     

Organic matter stabilization in a Xanthic Ferralsol of the central Amazon as affected by single trees: chemical characterization of density,aggregate, and particle size fractions

Not only the amount of organic carbon in soil is important for soil organic matter (SOM) stability, but also its physical and chemical properties. The appropriate technique for the assessment of SOM dynamics can vary between soil types, and information about this is lacking for Ferralsols of the central Amazon basin. First, this work identified SOM pools which are sensitive to land-use changes on the terra firme in the central Amazon. In a second step, the effects of single trees on SOM properties were evaluated in a mixed tree crop plantation in comparison to secondary and primary forest sites. Thus, the processes of organic matter stabilization could be studied in the highly aggregated soils. A combination of aggregate and density fractionation was found to be most suitable for physical SOM characterization. The particulate organic matter (POM, density less than 1.6 Mg m⁻³) varied by one order of magnitude between sites and could be used as a sensitive indicator of land-use changes. Aggregate stability was not related to SOM contents or bulk SOM properties. The incorporation of plant material into stable SOM, however, was enhanced by aggregation. Among aggregate separates, the fraction, 0.25–0.5 mm, showed single-tree effects the most. SOM replenishment was higher under tree species with low quality litter, i.e. high C-to-N and polyphenol-to-N ratios. High quality litter from a leguminous ground cover, however, showed low soil nitrogen and carbon replenishment but increased nitrogen concentrations in light fractions. Litter with a high quality may improve soil nitrogen availability but not amounts of total SOM, which could only be shown for low quality litter. The results indicate the importance of aggregation and POM dynamics for SOM stabilization in the studied Xanthic Ferralsols of the central Amazon basin.     

Long‐Term Tillage and Cropping System Effects on Chemical and Biochemical Characteristics of Soil Organic Matter in a Mediterranean Semiarid Environment

Several studies have reported how tillage and cropping systems affect quantity, quality, and distribution of soil organic matter (SOM) along the profile. However, the effect of soil management on the chemical structure of SOM and on its hydrophobic and hydrophilic components has been little investigated. In this work, the long‐term (19 years) effects of two cropping systems (wheat monoculture and wheat/faba bean rotation) and three tillage managements (conventional, reduced, and no tillage) on some chemical characteristics of SOM and their relationships with labile carbon (C) pools were evaluated. Soil samples were taken from the topsoil (0–15 cm) of a Chromic Haploxerert (central Sicily, Italy). After 19 years of different tillage and cropping systems management, total organic C significantly differed among treatments with the labile organic C pools showing the greater amount in no till and in wheat/faba bean plots. Hydrophobic and hydrophilic components of SOM, determined by diffuse reflectance infrared Fourier transform spectroscopy, were mainly affected by cropping system, whereas aromatic components of SOM by tillage. Soil organic matter components and characteristics showed significant correlations with the soil biochemical parameters, confirming the expected synergism between chemical and biochemical properties. This study demonstrated that (i) no tillage and crop rotation improve the chemical and biochemical properties of SOM of Vertisols under semiarid environment; and (ii) tillage management and cropping systems have affected, after 19 years, more the chemical and biochemical properties of SOM than its quantity. Copyright © 2014 John Wiley & Sons, Ltd.     

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.     

Effect of soil pH on the chemical composition of organic matter in physically separated soil fractions in two broadleaf woodland sites at Rothamsted,UK

Although acid soils are common in forest ecosystems, and there is documented evidence of pH influencing transformations of organic matter in soil, there are surprisingly few studies on the influence of soil pH on the chemical structure of physically fractionated soil organic matter (SOM). The aim of this study was to characterize the influence of pH on the chemical and physical processes involved in SOM stabilization. Forest soils of different pH (4.4 and 7.8) sampled from two long‐term experiments at Rothamsted Research (UK) were physically fractionated. The free light fraction (FLF), the intra‐aggregate light fraction and the fine silt and clay (S + C, <25 µm) were characterized using elemental, isotopic (δ¹³C), thermogravimetric, differential thermal, diffuse reflectance infrared Fourier transform spectroscopy and high‐resolution magic angle spinning ¹H nuclear magnetic resonance analyses. The quantitative distribution of carbon (C) between SOM fractions differed between the two soils. Carbon contents in the light fractions from the acid soil were significantly greater than in those of the alkaline soil. In contrast, in S + C fractions, C content was greater in the alkaline soil. FLF from the acid soil was characterized by a greater C:N ratio, smaller δ¹³C and greater content of thermo‐labile compounds compared with FLF from the alkaline soil. In contrast, there was only a weak effect of soil pH on the chemical composition of the organic matter in S + C fractions. Irrespective of soil pH, these latter fractions contained mainly aliphatic compounds such as carbohydrates, carboxylic acid, amide and peptide derivates. This suggested that physical mechanisms, involving the interactions between SOM and mineral surfaces, are of greater importance than the presence of chemically recalcitrant species in protecting SOM associated with the finest soil fractions.     

变性土的形态发生: 模型研究

Studies on Vertisols of Southwest China show that the distribution of organic matter, mechanical composition, carbonates and spore-pollen in their profiles exhibits a definite differentiation and the radiocarbon age has a functional variation with soil depth, which suggests that pedoturbation model is a kind of incomplete model for genetic study and that the disturbance and inversion of solums of Vertisol are not as rapid and absolute as expected. In further consideration of the characters of swelling pressure and shear strength of Vertisol, vertic soil and other zonal soils, it is speculated that soil mechanics model is more adaptable for interpreting the morphogenesis of Vertisols without any contradiction with soil properties.     

Organic matter in volcanic soils in Chile: Chemical and biochemical characterization

Abstract

Determinations were made of total soil organic matter (SOM), stable and labile organic fractions, biomass carbon (C), and chemical composition of several humus‐soil‐fractions in Chilean volcanic soils, Andosols and Ultisols. Their physico‐chemical properties and humification degree at different stages in edaphic evolution were also assessed. In addition, organic matter models were obtained by chemical and biological syntheses and the structures and properties of natural and synthetic humic materials were compared with SOM. Results indicate that Andosols have higher SOM levels than Ultisols, but the fraction distribution in the latter suggests a shift of the more stable fractions to the more labile ones. Moreover, contents of humines, and humic and fulvic acids suggest that Chilean volcanic soil SOM is highly humified. On the other hand, among the SOM labile fractions, carbohydrate and biomass are about 15% of the SOM which are one of the most important fractions in soil fertility.     

Factors affecting the molecular structure and mean residence time of occluded organics in a lithosequence of soils under ponderosa pine

Occluded, or intra-aggregate, soil organic matter (SOM) comprises a significant portion of the total C pool in forest soils and often has very long mean residence times (MRTs). However, occluded C characteristics vary widely among soils and the genesis and composition of the occluded organic matter pool are not well understood. This work sought to define the major controls on the composition and MRT of occluded SOM in western U.S. conifer forest soils with specific focus on the influence of soil mineral assemblage and aggregate stability. We sampled soils from a lithosequence of four parent materials (rhyolite, granite, basalt, and dolostone) under Pinus ponderosa. Three pedons were excavated to the depth of refusal at each site and sampled by genetic horizon. After density separation at 1.8 g cm⁻³ into free/light, occluded and mineral fractions, the chemical nature and mean residence time of organics in each fraction were compared. SOM chemistry was explored through the use of stable isotope analyses, ¹³C NMR, and pyrolysis GC/MS. Soil charcoal content estimates were based on ¹³C NMR analyses. Estimates of SOM MRT were based on steady-state modeling of SOM radiocarbon abundance measurements. Across all soils, the occluded fraction was 0.5–5 times enriched in charcoal in comparison to the bulk soil and had a substantially longer MRT than either the mineral fraction or the free/light fraction. These results suggest that charcoal from periodic burning is the primary source of occluded organics in these soils, and that the structural properties of charcoal promote its aggregation and long-term preservation. Surprisingly, aggregate stability, as measured through ultrasonic dispersion, was not correlated with occluded SOM abundance or MRT, perhaps raising questions of how well laboratory measurements of aggregate stability capture the dynamics of aggregate turnover under field conditions. Examination of the molecular characteristics of the occluded fraction was more conclusive. Occluded fraction composition did not change substantially with soil mineral assemblage, but was increasingly enriched in charcoal with depth relative to bulk SOM. Enrichment levels of ¹³C and ¹⁵N suggested a similar degree of microbial processing for the free/light and occluded fractions, and molecular structure of occluded and free/light fractions were also similar aside from charcoal enrichment in the occluded fraction. Results highlight the importance of both fire and aggregate formation to the long-term preservation of organics in western U.S. conifer forests which experience periodic burning, and suggest that the composition of occluded SOM in these soils is dependent on fire and the selective occlusion of charcoal.     

Changes in soil properties and humic substances after long‐term amendments with manure and crop residues in dryland farming systems

After 16 years of periodical applications of either farmyard manure or crop wastes at two levels of mineral N fertilization to a Calcic Haploxeralf in the semiarid central Spain, we found significant changes in chemical fertility levels and in the concentration, chemical composition, and carbon mineralization rates of soil organic matter (SOM). The changes in SOM quality were related to significant improvements of soil physical properties, mainly aggregate stability and water retention. Such changes were related to the increased concentration of humic colloids in soil, the mineral N dose, and the type of organic matter applied. When compared with the control plots, the organic matter accumulated in the amended plots tended to be less transformed, and its total concentration and humification degree decreased with increasing external N‐inputs. Humic acids from the amended plots showed a more marked aliphatic character (mainly after N addition) than those from control plots. Farmyard manure led to a significant improvement of soil physical properties, but had a comparatively small effect in promoting biodegradation and humification of crop wastes. This could be due to the high biological stability of the manure used which, in semiarid Mediterranean fields, usually leads to an accumulation of little transformed SOM.     

应用~(13)C核磁共振技术研究土壤有机质化学结构进展

土壤有机质化学结构对准确评价土壤有机质的稳定性及其在土壤中的功能具有重要意义。土壤有机质化学结构的研究方法中,固态~(13)C核磁共振波谱技术(Solid-state ~(13)C-NMR spectroscopy)具有独特优势,对土壤有机质化学结构的解析更贴近真实状态,近年来已取得诸多新进展和新突破。综述了近年来应用~(13)C-NMR测定土壤全土、团聚体和密度组分、腐殖质组分的有机碳化学结构特征,分析了影响化学结构变化的因素。不同气候条件、植被类型、土地利用管理方式、土壤类型、土壤有机碳含量的全土中有机碳化学结构比较相似,均表现为烷氧碳比例最高,其次为烷基碳和芳香碳,羧基羰基碳比例最低。土壤有机碳主要来源于外源植物残体,植物残体化学结构的相似性可能是导致土壤有机碳化学结构相似的主要原因,环境条件、土壤自身属性和微生物活性的差异使土壤有机碳化学结构产生微小差异。土壤颗粒及化学组分间的有机碳分子结构差异较大,大颗粒有机碳中烷氧碳比例最高,小粒径及与矿物颗粒结合的有机碳中烷基碳和羧基羰基碳比例更高,粉黏粒和腐殖酸组分的有机碳化学结构在土壤类型间差异较大。今后的研究重点应更多地关注土壤有机质来源的定量化分析、土壤微生物对土壤有机碳组分和结构稳定性的贡献及调控机制、土壤有机碳稳定性的生物物理化学保护机制、空间大尺度环境因子/土壤生态过程与微观尺度的有机碳化学分子结构的耦合作用机制、跨学科的多种土壤有机碳化学分子结构测定辨识技术等方面的研究。     

Carbon isotopes of water‐extractable organic carbon in a depth profile of forest soil imply a dynamic relationship with soil carbon

Although considerable research has been conducted on the importance of recent litter compared with older soil organic matter as sources of dissolved organic carbon (DOC) in forest soils, a more thorough evaluation of this mechanism is necessary. We studied water‐extractable organic carbon (WEOC) in a soil profile under a cool‐temperate beech forest by analysing the isotopic composition (¹³C and ¹⁴C) of WEOC and its fractions after separation on a DAX‐8 resin. With depth, WEOC became more enriched in ¹³C, which reflects the increasing proportion of the hydrophilic, isotopically heavier fraction. The ¹⁴C content in WEOC and its fractions decreased with depth, paralleling the ¹⁴C trend in soil organic matter (SOM). These results indicate a dynamic equilibrium of WEOC and soil organic carbon. The dominant process maintaining the WEOC pool in the mineral soil appears to be the microbial release of water‐soluble compounds from the SOM, which alters in time‐scales of decades to centuries.     

Location and chemical composition of stabilized organic carbon in topsoil and subsoil horizons of two acid forest soils

The ¹⁴C age of soil organic matter is known to increase with soil depth. Therefore, the aim of this study was to examine the stabilization of carbon compounds in the entire soil profile using particle size fractionation to distinguish SOM pools with different turnover rates. Samples were taken from a Dystric Cambisol and a Haplic Podzol under forest, which are representative soil types under humid climate conditions. The conceptual approach included the analyses of particle size fractions of all mineral soil horizons for elemental composition and chemical structure of the organic matter by ¹³C cross-polarization magic angle spinning nuclear magnetic resonance (CPMAS NMR) spectroscopy. The contribution of phenols and hydroxyalkanoic acids, which represent recalcitrant plant litter compounds, was analyzed after CuO oxidation.In the Dystric Cambisol, the highest carbon concentration as well as the highest percentage of total organic carbon are found in the <6.3 μm fractions of the B and C horizons. In the Haplic Podzol, carbon distribution among the particle size fractions of the Bh and Bvs horizons is influenced by the adsorption of dissolved organic matter. A relationship between the carbon enrichment in fractions <6.3 μm and the ¹⁴C activity of the bulk soil indicates that stabilization of SOM occurs in fine particle size fractions of both soils. ¹³C CPMAS NMR spectroscopy shows that a high concentration of alkyl carbon is present in the fine particle size fractions of the B horizons of the Dystric Cambisol. Decreasing contribution of O-alkyl and aromatic carbon with particle size as well as soil depth indicates that these compounds are not stabilized in the Dystric Cambisol. These results are in accordance with data obtained by wet chemical analyses showing that cutin/suberin-derived hydroxyalkanoic acids are preserved in the fine particle size fractions of the B horizons. The organic matter composition in particle size fractions of the top- and subsoil horizons of the Haplic Podzol shows that this soil is acting like a chromatographic system preserving insoluble alkyl carbon in the fine particle size fractions of the A horizon. Small molecules, most probably organic acids, dominate in the fine particle size fractions of the C horizons, where they are stabilized in clay-sized fractions most likely due to the interaction with the mineral phase. The characterization of lignin-derived phenols indicated, in accordance with the NMR measurements, that these compounds are not stabilized in the mineral soil horizons.     

Distribution of stable carbon isotopes in an agrochernozem during the transition from C3 vegetation to a corn monoculture

The distribution of carbon in an agrochernozem??s profile was studied by the natural ¹³C abundance method during the C₃-C₄ vegetation transition and the analysis of the soil phytolith complex under a continuous corn monoculture. A young pool of soil organic matter (SOM) formed during 43 years of monoculture growing was detected by the isotope analysis in the 0-to 60-cm layer, while the analysis of the phytolith complex identified this pool deeper: corn phytoliths were detected in the 0- to 80-cm layer. The maximum size of the young pool was found in the upper soil horizon; it reached 6.4% of the SOM in the 0- to 20-cm layer. The apparent time of the SOM turnover was 635 and 2225 years in the 0- to 20- and 40- to 60-cm layers, respectively. The high values of the mean residence time were related to the low input of plant residues to the soil at the growing of corn for silage and the high initial content of organic carbon in the chernozem. The changes in the isotope composition after the decalcification of the soil to remove carbonates and the variation of the ??¹³C in the corn biomass during the vegetation period significantly affected the calculated value of the mean residence time.     

Characterization of hydrophobic acid fractions in water-soluble organic matter in Dystric Cambisol and in a stream in a small forested watershed: Seasonal and vertical variations in chemical properties

Abstract

Chemical properties of hydrophobic acid (HoA) fractions in water-soluble organic matter in soil and water are concerned with its interactions with mineral soil surfaces and organic pollutants. In 2004 we examined the seasonal and vertical changes in chemical properties of the HoA fraction in a Cambisol profile and compared these properties with those in the HoA fraction of an adjacent stream (aquatic humic substances) in a temperate forested watershed using high performance size exclusion chromatography (HPSEC) and ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy. The HoA fractions from Oi, Oe/Oa, A and B horizon soils in summer had lower O-alkyl C proportions than those recorded in samples in other seasons. The proportions of aromatic C in HoA fractions from A and B horizons were highest in summer. These seasonal variations were less significant than variations with soil depth. O-alkyl C proportions in HoA fractions decreased with increasing soil depth from the Oi to the A horizon. The HoA fractions from the B horizon showed a higher alkyl C proportion than samples from other horizons in winter and spring. These changes with soil depth from the Oi to A horizons might result from selective utilization of carbohydrate carbon by microorganisms, whereas those in the B horizon may result from sorption to mineral surfaces. The HoA fractions in the stream were similar in relative molecular weight, distribution of each type of proton and carbon species in HoA fractions from the B horizon, whereas stream HoA fractions collected in summer would be derived from organic horizons. This indicated that vertical changes in the chemical properties of HoA fractions in soil and pathways of water to the stream would largely affect the chemical properties of HoA fractions in the stream.     

Vertigenesis in soils of the central chernozemic region of Russia

On the basis of soil studies along routes and on key plots, 35 new areas of soils with definite features of vertigenesis have been identified in Belgorod and Voronezh oblasts and in the northern part of Volgograd oblast (in the Don River basin). Earlier, vertic soils were not noted for these areas. In the studied region, their portion in the soil cover is much less than 1%. All the delineated areas of vertic soils are confined to the outcrops of swelling clay materials of different origins (marine, lacustrine, glacial, and colluvial sediments) and ages (Quaternary or Tertiary) that may be found in four landscape positions: (1) in the deep closed depressions within vast flat watersheds; (2) in the bottoms of wide hollows on interfluvial slopes and, sometimes, on steeper slopes of local ravines; (3) in the hydromorphic solonetzic soil complexes, and (4) on step-like interfluvial surfaces with the outcrops of Tertiary clays. Within the studied areas, soils with different degrees of expression (six grades) of vertic properties are present. These soils belong to the type of dark vertic soils proper and to vertic subtypes of different soil types according to the Russian soil classification system; according to the WRB system, they belong to Vertisols proper and to reference soil units with a Vertic prefix in the groups of Chernozems, Phaeozems, and Solonetzes. Statistical data on the morphometric indices of the vertic properties (the depth and thickness of the soil horizons with slickensides, a wedge-shaped structure, and cracks filled with material from the upper horizons) and the depth and thickness of the Vertic horizon are analyzed.     

MINERALOGY AND CHEMISTRY OF A TRANSVAAL BLACK CLAY TOPOSEQUENCE

Moralistic soils (vertic and non-vertic black clays) were sampled along a 200 m top sequence in the Transvaal Highveld, South Africa. The Milk wood soil on the upper part of the margalitic top sequence has an Al horizon which lacks both slickensides and self-mulching properties but has strong blocky structure, the others are all self-mulching (i.e. Vertisols). The Vertisols differ in some morphological properties such as the absence (Mngazi series) and presence (Arcadia series) of pedogenic calcite accumulation, both overlying decomposed dolerite, whereas the third member from a red-black centenary sequence is calcareous with a gleyed subsoil horizon. Chemical and XRD analysis suggest that the clays of the Vertisols comprise mainly a partly chloritized iron-rich smectite with Ie > Mg + Al in the octahedral layer (and interlayer positions), while in the upland Milkwood soil intergradient halloysitic clay occurs in addition to a more‘open’structured chloritized iron smectite. The mineralo-chemical results and the geomorphic data suggest that the genesis of these soils is controlled primarily by the internal soil water regime.     

土壤理化性质异质性研究及其影响

Structured soils are characterized by the presence of inter- and intra-aggregate pore systems and aggregates, which show varying chemical, physical, and biological properties depending on the aggregate type and land use system. How far these aspects also affect the ion exchange processes and to what extent the interaction between the carbon distribution and kind of organic substances affect the internal soil strength as well as hydraulic properties like wettability are still under discussion. Thus, the objective of this research was to clarify the effect of soil aggregation on physical and chemical properties of structured soils at two scales： homogenized material and single aggregates. Data obtained by sequentially peeling off soil aggregates layers revealed gradients in the chemical composition from the aggregate surface to the aggregate core. In aggregates from long term untreated forest soils we found lower amounts of carbon in the external layer, while in arable soils the differentiation was not pronounced. However, soil aggregates originating from these sites exhibited a higher concentration of microbial activity in the outer aggregate layer and declined towards the interior. Furthermore, soil depth and the vegetation type affected the wettability. Aggregate strength depended on water suction and differences in tillage treatments.