Water-soluble low-molecular-weight organic acids in automorphic loamy soils of the tundra and taiga zones

The formation features of water-soluble low-molecular-weight organic acids (LMWOAs) in a zonal series of automorphic soils on loose silicate rocks from the middle taiga to the southern tundra (typical podzolic, gley-podzolic, and surface-gley tundra soils) were first revealed by gas chromatography mass spectrometry and gas-liquid chromatography. The content of LMWOAs varies within the range of 1–14 mg/dm³, which corresponds to 1–5% of the total carbon of the water-soluble soil organic matter. It has been shown that a subzonal feature of gley-podzolic soils in the northern taiga is the high content of LMWOAs, including primarily the strongest aliphatic hydroxyl acids. Possible mechanisms of their formation and accumulation in soils have been considered.     

A new method to determine the carbon content of water-soluble organic compounds in soils

The possibility to use the oxidation rate of different waters by dichromate as measured by photometry for the determination of the organic carbon content in water extracts from the organic horizons of soddy-podzolic soils (in the Republic of Komi) was confirmed. The advantages of the method proposed are discussed.     

Transformation of nitrogen compounds in the tundra soils of Northern Fennoscandia

The transformation of organic nitrogen compounds in the soils of tundra ecosystems of Northern Fennoscandia has been studied under laboratory and natural conditions. Tundra soils contain significant reserves of total nitrogen, but they are poor in its extractable mineral and organic forms. The potential rates of the net mineralization and net immobilization of nitrogen by microorganisms vary among the soils and depend on the C: N ratio in the extractable organic matter and microbial biomass of soil. Under natural conditions, the rate of nitrogen net mineralization is lower than the potential rate determined under laboratory conditions by 6–25 times. The incubation of tundra soils in the presence of plants does not result in the accumulation of mineral nitrogen compounds either in the soil or in microbial biomass. This confirms the high competitive capacity of plants under conditions of limited nitrogen availability in tundra ecosystems.     

低分子量有机酸对可变电荷土壤铝活化动力学的影响

从动力学角度研究了几种低分子量有机酸对2种酸性土壤中铝的活化和活化铝在土壤固/液相之间分配的影响。结果表明:对于络合能力弱的醋酸和乳酸,主要通过质子作用活化铝,且活化作用明显小于盐酸。而络合能力较强的苹果酸、草酸和柠檬酸,主要通过络合作用促进铝的释放,且这种作用随有机酸根阴离子络合能力的增强而增加。在氧化铁含量较高的砖红壤中,苹果酸、草酸和柠檬酸通过专性吸附增加土壤表面负电荷,从而增加土壤交换态铝;但在氧化铁含量较低的红壤中,草酸和柠檬酸主要通过形成可溶性铝络合物降低交换态铝。活化铝在土壤固/液相间的分配主要决定于溶液中有机阴离子与土壤固相表面对铝离子的竞争。醋酸和乳酸活化的铝主要以交换态铝存在;而草酸和柠檬酸活化的铝主要以有机酸-铝络合物存在于溶液中,特别是在氧化铁低的红壤中,这将促进铝在土壤-水体中的迁移。     

Sulfate adsorption by variable charge soils: Effect of low-molecular-weight organic acids

Sulfate (SO₄ ^2–) movement and transport in soils has received considerable attention in recent years. In most soils, SO₄ ^2– coexists with a variety of natural organic compounds, especially organic acids. Studies were conducted to assess the effect of low-molecular-weight organic acids (eight aliphatic and five aromatic acids) on SO₄ ^2– adsorption by variable charge soils from Chile and Costa Rica. The effects of type of organic acid, pH, type of soil, and organic acid concentration were investigated. In one experiment, a 1.0 g soil sample was equilibrated with 25 ml 0, 0.5, 1.0, 2.0, 4.0, or 6.0 mM K₂SO₄ in 1 mM NaCl in the presence or absence of 5 mM citric acid. In the second set of experiments, the adsorption of 2 mM SO₄ ^2– in soils at pH 4 or pH 5 in the presence or absence of one of 13 organic acids at a concentration of 2 mM or 5 mM was studied. Results showed that citric acid significantly decreased SO₄ ^2– adsorption by the two soils. Sulfate adsorption decreased with increasing pH of the equilibrium solution. Aliphatic acids, with the exception of cis-aconitic acid, decreased the amount of SO₄ ^2– adsorbed by the two soils, with oxalic, tartaric, and citric acid showing the greatest effect. The differences in pH values of the equilibrium solutions in the presence and absence of organic acids were significantly, but negatively, correlated with the amount of SO₄ ^2– adsorbed, suggesting chemisorption of SO₄ ^2– and the release of hydroxide ions. The ionization fraction values of the organic acids at the equilibrium pH were correlated with the amounts of SO₄ ^2– adsorbed, suggesting that the protonation of surface hydroxyl groups of the mineral phase increased as the strength of the ionization of the acid increased, thus creating more positively charged surfaces. Received: 12 February 1997     

Effect of low-molecular-weight organic acids on Cl- adsorption by variable charge soils

Low-molecular-weight (LMW) organic acids exist widely in soils and have been implicated in many soil processes.The objective of the present paper was to evaluate effect of two LMW organic acids, citric acid and oxalic acid, on Cl^- adsorption by three variable charge soils, a latosol, a lateritic red soil and a red soil, using a batch method. The results showed that the presence of citric acid and oxalic acid led to a decrease in Cl- adsorption with larger decreases for citric acid. Among the different soils Cl- adsorption in the lateritic red soil and the red soil was more affected by both the LMW organic acids than that in the latosol.     

Effect of water composition on phosphorus concentration in runoff and water-soluble phosphate in two grassland soils

Many irrigation experiments determine phosphorus (P) losses from soil. Often, these studies cannot be compared, because the irrigation water was not characterized. We used calcium‐rich tap water and deionized water to investigate the influence of water composition on P concentrations in induced runoff. We irrigated two grassland sites: one acid and one calcareous. Less P was measured in runoff from tap water irrigation than from deionized water, especially for the acid soil. Batch experiments confirmed the findings of the field experiments. Tap water decreased water‐soluble phosphate and increased calcium in the solid phase. This interaction increased with decreasing soil:water ratio. Water of low ionic strength gave results comparable to rainwater. Our findings demonstrate that solution chemistry and the soil:water ratio can strongly influence the availability of P for transport. We recommend that P tests or irrigation experiments should use water resembling that of the system of interest. Irrigation experiments aiming to simulate P losses by surface runoff should be carried out with water having a composition comparable to rainwater.     

Psychrotolerant actinomycetes of plants and organic horizons in tundra and taiga soils

It has been revealed that in organic horizons and plants of the tundra and taiga ecosystems under low temperatures, actinomycetal complexes form. The population density of psychrotolerant actinomycetes in organic horizons and plants reaches tens and hundreds of thousands CFU/g of substrate or soil, and decreases in the sequence litters > plants > soils > undecomposed plant remains > moss growths. The mycelium length of psychrotolerant actinomycetes reaches 220 m/g of substrate. Application of the FISH method has demonstrated that metabolically active psychrotolerant bacteria of the phylum Actinobacteria constitute 30% of all metabolically active psychrotolerant representatives of the Bacterià domain of the prokaryotic microbial community of soils and plants. Psychrotolerant actinomycetes in tundra and taiga ecosystems possess antimicrobial properties.     

Chemical composition of water-soluble fraction in soils on glaciolacustrine deposits of the Russian Plain

The behavior of some chemical elements was studied in soils and their liquid phase. Two reference soil profiles on glaciolacustrine clays (soddy-eluvial-metamorphic soil) and sands (soddy podzol) were investigated on the Russian Plain. A colloidal fraction (particles <1 μm) was isolated with deionized hot water from a soil sample of 30 g at the soil: water ratio of 1: 10. The suspension was mixed for 6 h, settled for 24 h, and filtrated using a membrane filter (<1 μm). The soil sample and its water-soluble fraction (WSF) were analyzed by mass spectrometry with inductively coupled plasma. The chemical characteristics of the extracted liquid phase of the soil reflect its water-soluble component properties. The comparison of the data obtained with the results of the analysis for the whole soil allows assessment of a share of easily mobile and difficultly mobile forms of chemical compounds. This is the necessary basis for the development of a model describing the transport of metals in soil.     

Polycyclic aromatic hydrocarbons in soils and lower-layer plants of the southern shrub tundra under technogenic conditions

In soils and plants of the southern shrub tundra, 15 polycyclic aromatic hydrocarbons (PAHs) have been detected by high-performance liquid chromatography. Polyarenes in emissions, soil organic horizons, and plants mainly include low-molecular-weight PAHs: naphthalene, fluorine, and pyrene. The contents of the total PAHs in soils and plants exceed the background levels by 3–5 times. The distribution of polyarenes among the organs of the studied plants is nonuniform and depends on the plant species and technogenic load on the area. The studied plants include both hyperaccumulators of polyarenes (Pleurozium schreberi) and indicators of PAHs in the soil (Polytrichum commune). Pleurozium schreberi is the most abundant species in the areas under study, and it accumulates the largest mass fraction of PAHs. The differences in the accumulation of PAHs by the plants of the tundra and taiga zones have been revealed.     

Effect of the natural reforestation of an arable land on the organic matter composition in soddy-podzolic soils

The dynamics of the organic matter composition in soddy-podzolic soils during the natural reforestation of an arable land in the southern taiga zone have been discussed. It has been shown that the contents of the total and labile carbon in the old plow horizon increase with the age of the fallow in the chronosequence of soils established in the Parfen’evo district of Kostroma oblast. The parameters characterizing the labile soil organic matter include the contents of the carbon extractable by mild chemical extractants (distilled water, 0.1 M K₂SO₄ solution, 0.1 M neutral Na₄P₂O₇ solution), the microbial biomass, and the light fraction. The granulo-densimetric fractionation has shown that the contents of carbon in the light and organomineral fractions of the soil vary in the course of the postagrogenic succession. The content of the clay-fraction carbon increases and its portion in the total carbon of the soil decreases at the transition from the plowland to the forest. The reforestation of agrosoddy-podzolic soils enhances the physical protection of the soil organic matter due to the increase in the portion of microaggregate carbon.     

土壤水溶性有机物质的吸附、氧化和复合反应

A greater part of water-soluble organic substances,accounting for 60-70% of the total,could be adsorbed by soils,which included strongly and weekly reducing substances,positively and negatively charged substances and substances containing amido.There existed a tendency of decrease in adsorption of the negatively charged organic substances by the soil from South China to North China,with expression as Coulombian adsorption.A simulatneous reduction of iron and manganese appeared with clear voltammertric behaviours upon oxidation of water-soluble organic substances,Complexation of organic ligands with ferrous iron and manganous manganee was proved by differential pulse voltammetric method,with disappearance of oxidation peaks of ferrous iron and manganous manganese at 0.00 V and 0.35 V and occurrence of Fe^2 -complex and Mn^2 -complex at 0l75 V and 1.2V respectively,whose peak potentials shifted backward.     

Microbial transformation of nitrogen compounds in soils of the southern taiga

The intensity of the processes of nitrogen mineralization, fixation, and denitrification was assessed in the high-moor peat gley, white-podzolic, pale-podzolic, burozem, low-moor peat, and soddy-gley soils of the Central Forest Biosphere Reserve (CFBR). The actual and potential activities of the nitrogen fixation and denitrification were determined using the gas-chromatographic method, and the intensity of the ammonification was determined using ion-selective electrodes. The maximum intensity of the nitrogen fixation was observed in the low-moor peat and soddy-gley soils, which are characterized by a high content of organic matter. High denitrification activity was found in the low-moor peat soil (0.31 nmol N₂O/g per h); this was determined by the excessive moistening of this soil. The processes of organic nitrogen mineralization were the most intensive in the upper (L and F) subhorizons of the litter.     

Nonspecific organic compounds in peat soils of the Subpolar Urals

Specific features of organic matter, molecular composition and distribution of oxygen-containing nonspecific organic compounds (fatty acids, long-chain aliphatic alcohols, and ketones) were revealed in two peat soils on slopes of the Subpolar Urals: the eutrophic peat soil of the spring mire (Hemic Histosols) and the peat soil of a slope mire (Fibric Histosols). Compounds that can serve as molecular markers for some evolutionary stages of peats were determined for this area. Based on the data obtained, the most probable causes of differences in the composition of organic compounds in the peats studied were found to be the following: environmental conditions, water and mineral regime of bog, and differences in the composition of peat-forming plants.     

Molecular composition of humic substances in tundra soils (13C-NMR spectroscopic study)

Functional groups and molecular fragments of humic substances (HSs) from cryohydromorphic peat gley tundra and surface-gley tundra soils have been identified by ¹³C-NMR spectroscopy. The analysis of HS preparations has shown that the molecules of humic acids (HAs) are enriched with aromatic fragments compared to fulvic acids (FAs). Aliphatic chains, carbohydrate- and amino acid-type structures prevail in the carbon skeleton of the FAs. An integrated parameter of the HS hydrophobicity has been proposed. The parameter represents the total portion of unoxidized carbon atoms and allows indirectly assessing the amphiphilic properties of HSs.     

低分子量有机酸对促进可变电荷土壤中铝溶解的影响

Low-molecular-weight （LMW） organic acids exist widely in soils and play an important role in soil processes such as mineral weathering, nutrient mobilization and A1 detoxification. In this research, a batch experiment was conducted to examine the effects of LMW organic acids on dissolution of aluminum in two variably charged soils, an Ultisol and an Oxisol. The results showed that the LMW organic acids enhanced the dissolution of A1 in the two investigated soils in the following order： citric 〉 oxalic 〉 malonic 〉 malic 〉 tartaric 〉 salicylic 〉 lactic 〉 maleic. This was generally in agreement with the magnitude of the stability constants for the Al-organic complexes. The effects of LMW organic acids on Al dissolution were greater in the Ultisol than in the Oxisol as compared to their controls. Also, the accelerating effects of citric and oxalic acids on dissolution of A1 increased with an increase in pH, while the effects of lactic and salicylic acids decreased. Additionally, when the organic acid concentration was less than 0.2 mmol L-I, the dissolution of A1 changed Iittle with increase in acid concentration. However, when the organic acid concentration was greater than 0.2 mmol L^-1,the dissolution of A1 increased with increase in acid concentration. In addition to the acid first dissociation constant and stability constant of Al-organic complexes, the promoting effects of LMW organic acids on dissolution of A1 were also related to their sorption-desorption equilibrium in the soils.     

Features of cryogenic environment in soils of continental tundra and arid steppe on the southern Khangai slope under electron microscope

Morphoscopic studies were conducted with the aid of SEM and TEM microscopes, on quartz grains and fractions not exceeding 2 μm, on soil samples from the continental tundra, alpine meadow and arid steppe. The aim of these studies was to define the features and properties of the quartz grains and fractions, produced by the environment of the cryoarid continental climate of Central Asia. It has been established that in cold and humid climates processes of cryogenic and hydrothermic splitting occur on the surface of quartz grains and in cold and dry climates processes of cryothermic scalling. The increase in the surface area of disintegrated minerals under continental climate conditions is accompanied by cryochemical coating by mineral-organic compounds.     

Volatile organic compounds (VOCs) in soils

Soils may act as sources or sinks of volatile organic compounds (VOCs). Many of the formed VOCs are produced by microorganisms, and it would be a challenge to investigate soil microbial communities by studying their VOC profile. Such “volatilomics” would have the advantage of avoiding extraction steps that are often a limit in genomic or proteomic approaches. Abundant literature on microbially produced VOCs is available, and in particular novel detection methods allow additional insight. The aim of this paper was to give an overview on the current knowledge of microbial VOC emissions from soils.     

土壤有机复合物降解的动力学模型

A set of equations in suggested to describe the kinetics of degradation of organic ompounds applied to soils ad the kinetics of growth of the inolved microorganisms:-dx/dt=jx kxm dm/dt=-fm gxm where x is the concentration of organic compound at time t,m is the numer of microorganisms capable of degrading the organic compound at time t,while j,k,f and g are positive constants,This model can satisfactorily be used to explain the degradation curve of organic compounds and the growth curve of the involved microorganisms.