Specific features of the ecological functioning of urban soils in Moscow and Moscow oblast

Urban soils (constructozems) were studied in Moscow and several cities (Dubna, Pushchino, and Serebryanye Prudy) of Moscow oblast. The soil sampling from the upper 10-cm-thick layer was performed in the industrial, residential, and recreational functional zones of these cities. The biological (the carbon of the microbial biomass carbon, C_mic and the microbial (basal) respiration, BR) and chemical (pH_water and the contents of C_org, heavy metals, and NPK) indices were determined in the samples. The ratios of BR to C_mic (the microbial respiration quotient, qCO₂) and of C_mic to C_org were calculated. The C_mic varied from 120 to 738 μg C/g soil; the BR, from 0.39 to 1.94 μg CO₂-C/g soil per hour; the C_org, from 2.52 to 5.67%; the qCO₂, from 1.24 to 5.28 μg CO₂-C/mg C_mic/g soil per h; and the C_mic/C_org, from 0.40 to 1.55%. Reliable positive correlations were found between the C_mic and BR, the C_mic and C_mic/C_org, and the C_mic and C_org values (r = 0.75, 0.95, and 0.61, respectively), as well as between the BR and C_mic/C_org values (r = 0.68). The correlation between the C_mic/C_org and qCO₂ values was negative (r = −0.70). The values of C_mic, BR, C_org, and C_mic/C_org were found to correlate with the ammonium nitrogen content. No correlative relationships were revealed between the determined indices and the climatic characteristics. The principal component analysis described 86% of the variances for all the experimental data and clearly subdivided the locations of the studied soil objects. The ANOVA showed that the variances of C_mic, C_org, and BR are controlled by the site location factor by 66, 63, and 35%, respectively. The specificity of the functioning of the anthropogenic soils as compared with their natural analogues was clearly demonstrated. As shown in this study, measurable biological indices might be applied to characterize the ecological, environmental-regulating, and productive functions of soils, including urban soils.     

Postagrogenic transformation of organic matter in soddy-podzolic soils

In the chronological sequence of postagrogenic soils, the restoration of the original differentiation of the soil profile and its horizons proceeded with different rates depending on the fallow age and the horizon depth. The layer sampling (at 5-cm intervals) showed that the plow horizon began to differentiate into a system of subhorizons in all the fallow soils. The zonal pedogenesis showed clear signs of manifestation already in the 15-year-old fallow. The upper part of the former plow horizon in the 15- and 60-year-old fallows under herbaceous plants was transformed into a soddy horizon, while a postagrogenic soil 90 years old already developed under a zonal type of vegetation and approached the control soil in its morphological features. The content and reserve of carbon in the soils showed a stable tendency of increasing (especially in the upper part of the plow horizon) during the entire postagrogenic period under study. The water permeability of the soils gradually increased and approached that of the virgin soil. However, the compacted subsurface horizon (the plow pan) disappeared only after 90 years. The assessment of the physicochemical properties of the soils and the structural and functional parameters of the humic acids indicated the expansion of the layer differentiation primarily within the homogeneous plow horizon. From the elemental analysis and 13C NMR spectroscopy data, the degree of aromaticity in the molecular structure of the humic acids gradually decreased, and the aliphatic part developed with the age of the fallow.     

Recovery rate of organic c in organic matter fractions of Grantsburg soils

Abstract

Walkley‐Black method is a simple and rapid method for organic carbon analysis. Because of incomplete oxidation of organic carbon (C), the recovery of organic C is low with this method. Assuming the 77% recovery of organic C with Walkley‐Black method, the results are corrected with a correction factor of 1.30. The objective of this study is to determine the soil organic C recovery rate and appropriate correction factor for Walkley‐Black (wet combustion) method for tilled soils in southern Illinois. Soil samples were collected in 1995 and 1996 from a trial established in southern Illinois on a moderately well drained, Grantsburg (fine‐silty, mixed, mesic Oxyaquic Fragiudalf) soil. Organic C contents with the Leco analyzer (dry combustion) were significantly higher as compared to the Walkley‐Black method in different tillage systems (no‐till, chisel plow and moldboard plow), soil organic matter fractions (whole soil and mineral fraction) and soil depths (0–5 and 5–15 cm). The recovery percentage of organic C was lower than the assumed percentage with the Walkley‐Black method. No significant differences in organic C recovery percentage were found due to differences in tillage systems and depths, whereas the recovery percentage was lower in mineral fraction as compared to the whole soil. The lower organic C recovery percentage was due to the more stable organic C compounds in the mineral fraction. On the basis of these findings, correction factors of 1.35 and 1.41 are proposed for whole soil and mineral organic C analysis with Walkley‐Black method, respectively for tilled Grantsburg and other similar soils in southern Illinois.     

Specific features of the humus status in soils of Buryatia

The humus content in soils of Buryatia varies significantly in dependence on the local hydrothermic conditions. All the studied soils are characterized by a relatively short humus profile, a sharp drop in the humus content down the soil profile, considerable amounts of the humin fraction and the fraction of humic acids bound with sesquioxides, and a moderate humus enrichment with nitrogen.     

Specific stability of organic matter in a stormwater infiltration basin

Purpose

In stormwater infiltration basins, sediments accumulate at the soil surface and cause a gradual filling up of soil pores. These sediments are composed of a mixture of natural and anthropogenic (as oil products) organic matters (OMs). The degradation kinetics of these sediment OMs and their biological stability has been neglected. This study aimed to characterize sediments OMs to assess their evolution and their capacity to degrade.

Materials and methods

To characterize OMs from the sediment layer, we measured at several places in the infiltration basin, total OM and carbon (C) contents, C distribution and biochemical fractions of the OM in the different size fractions, the sediment’s C mineralization potential, soil microbial biomass, and organic pollutants (polycyclic aromatic hydrocarbons (PAHs)) in the sediment layer.

Results and discussion

OM contents were high and varied from 66 to 193 g?kg^?1 from the inlet to the outlet of basin. Depending on rainfall intensity and volume, organic particles were deposited at varying distances in the basin by decantation; this was confirmed by analysis of sediment C distribution in the different size fractions. Despite high amounts of OM, organic C had a low biodegradability. Mineralization potentials were low compared to natural soil (i.e., from 0.3 to 1.1 g CO₂–C kg^?1 total organic carbon). Biochemical fractionation of the organic fractions indicated that they were mainly composed of a soluble fraction, which contributed to reducing OM biodegradability. The activity of the sediment microbial biomass was low. PAH contents seemed to be partly responsible for the high biostability of OMs.

Conclusions

There was limited capacity for biodegradation of sediment OMs probably due to inhibitory effects of soluble PAHs and consequently low microbial activity.     

Pyrogenic transformation of organic matter in soils of forest bogs

Natural fires on forest bogs significantly affect all the groups and fractions of peat organic matter. The type and intensity of the fires are responsible for the depth of the pyrogenic transformation of peat. In the course of thermal destruction of peat organic matter, humus substances (humic acids in particular) are accumulated, which leads to changes in the type of humus; the humus reserves may increase by 1.5–8 times. Several ways of the formation of humus components related to the intensity of a fire are suggested. The regressive evolution of bog ecosystems caused by fires is a reversible process. The humus status of pyrogenically transformed horizons and their morphology are preserved within the peat deposit as a relic characteristic of the discrete metamorphosis of the soils.     

Mobilization and immobilization of dissolved organic matter in forest soils

Field and laboratory studies combined with destructive and nondestructive analytical methods were used to characterize dissolved organic matter (DOM) in acid forest soils. DOM is produced in significant amounts in the forest canopy and in the forest floor. A major part of the organic solutes are lignocellulose-degradation products being strongly microbially altered in the course of ligninolysis. The release of lignin-derived moieties into the soil solution is controlled by their degree of biooxidation. Microorganisms contribute also directly to the organic solutes through the release of microbial metabolites. DOM released from the forest floor passes the upper mineral soil almost conservatively, whereas in the subsoil most DOM is removed from solution. Immobilization of DOM is mainly due to sorption on Fe and Al oxides. The highly oxidized lignin-derived moieties are preferentially removed from the soil solution whereas the saccharides are relatively enriched. We conclude that DOM in the forest soil output to the hydrosphere is a result of (1) the release of microbially degraded lignocellulose compounds and of microbial metabolites into the forest floor solution and (2) selective sorptive removal of the lignin-derived constituents in the subsoil.     

Selenium retention in the organic matter of Swedish forest soils

Fractions of selenium present in the soil profiles of three Swedish podzols were analysed using a sequential extraction scheme to characterize Se distribution among the organic and inorganic fractions. The process by which selenite deposited from the atmosphere is retained in a podzolic profile rich in organic matter was studied in a column experiment. Selenium present in organic fractions accounted for most of the Se extracted by Na₄P₂O₇/NaOH. All soil organic matter fractions, particularly those in the B horizons, were considerably enriched with Se as compared with plant biomass. The most enriched fraction was that containing hydrophobic fulvates which had C to Se ratios ranging from 33 000 to 80 000. The distribution of Se among the organic fractions differed markedly from that of sulphur. Selenite applied to columns continuously for 67 d was fixed very rapidly upon entering the forest floor layers, with 77% being recovered in the top 2 cm of the forest floor after the experiment. In column leachates from the surface layers, C to Se ratios decreased progressively following Se application. No effect specifically related to Se application was observed for leachates and soil horizons underlying Bs1. The mechanism responsible for the efficient and rapid Se immobilization by organic matter is unknown.     

山东省苹果园土壤有机质及养分状况研究

通过大量田间采样分析了山东省三种主要土壤类型苹果园土壤的有效养分状况及其分布特点 ,结果表明 :三种土壤类型果园土中有效养分含量差异较大 ,棕壤富磷贫钾 ,潮土富钾贫磷 ,褐土介于二者之间 .不同土层间有效养分含量有较大差异 ,表层土 (0～ 2 0cm)含量最高 ,底层土 (4 0～ 60cm)含量最低 ;丰产园三土层间有效养分含量差异较少 ,低产园差异较大 ;丰产果园三土层氮磷钾比例的平均值为 :0～2 0cm1∶0 .53∶1 .59;2 0～ 4 0cm为 1∶0 .53∶1 .69;4 0～ 60cm为 1∶0 .51∶1 .72 .与 1 0年前相比 ,果园土壤有机质含量降低 ,有效氮磷钾含量增加 ,其中磷钾增幅较大 .     

Biological degradation of pyrogenic organic matter in temperate forest soils

Pyrogenic organic matter (PyOM), derived from the incomplete combustion of plant biomass and fossil fuels, has been considered one of the most stable pools of soil organic matter (SOM) and a potentially important terrestrial sink for atmospheric CO₂. Recent evidence suggests that PyOM may degrade faster in soil than previously thought, and can affect native SOM turnover rates. We conducted a six-month laboratory incubation study to better understand the processes controlling the degradation of PyOM in soils using dual-enriched (¹³C/¹⁵N) PyOM and its precursor wood (Pinus ponderosa). We examined the effects of soil type and inorganic N addition on PyOM and wood C and N mineralization rates, microbial C utilization patterns, and native SOM turnover rates. PyOM charred at 450 °C or its precursor pine wood was incubated in two temperate forest subsoils with contrasting short range order (SRO) clay mineralogy (granite versus andesite parent material). Duplicates of experimental treatments with and without PyOM added were sterilized and abiotic C mineralization was quantified. In a second incubation, PyOM or wood was incubated in granitic soil with and without added NH₄NO₃ (20 kg N ha⁻¹). The fate of ¹³C/¹⁵N-enriched PyOM and wood was followed as soil-respired ¹³CO₂ and total extractable inorganic ¹⁵N. The uptake of ¹³C from PyOM and wood by soil microbial community groups was quantified using ¹³C-phospholipids fatty acids (PLFA). We found that (1) The mean residence time (MRT) of PyOM-C was on a centennial time scale (390–600 yr) in both soil types; (2) PyOM-C mineralization was mainly biologically mediated; (3) Fungi more actively utilized wood-C than PyOM-C, which was utilized by all bacteria groups, especially gram (+) bacteria in the andesite (AN) soil; (4) PyOM-N mineralization was 2 times greater in granite (GR) than in AN soils; (5) PyOM additions did not affect native soil C or N mineralization rates, microbial biomass, or PLFA-defined microbial community composition in either soil; (6) The addition of N to GR soil had no effect on the MRT of C from PyOM, wood, or native SOM. The centennial scale MRT for PyOM-C was 32 times slower than that for the precursor pine wood-C or native soil C, which is faster than the MRT used in ecosystem models. Our results show that PyOM-C is readily utilized by all heterotrophic microbial groups, and PyOM-C and -N may be more dynamic in soils than previously thought.     

Labile ester sulphate in organic matter extracted from podzolic soils

Summary We studied the effect of soil pretreatment, molecular-weight fractionation, and K₂SO₄ addition on the concentration and biochemical stability of ester sulphate in soil organic matter. A labile ester sulphate fraction (8.1 g S g^–1 soil) was detected in the organic matter extracted from a sulphate-rich podzolic sandy loam. This fraction was susceptible to loss during soil pretreatment with water and KCl solution and subsequent extraction of organic matter from the soil. The low-sulphate loam was low in labile ester sulphate (0.6 g S g^–1 soil) and the pretreatments had little effect. The addition of K₂SO₄ to the organic matter extracted from the low-sulphate soil resulted in the formation of appreciable amounts of labile ester sulphate. Newly formed ester sulphate tends to be biochemically less stable than indigenous ester sulphate in soil humic polymers and the ester sulphate associated with the low molecular-weight fractoin of soil organic matter appears to be more susceptible to loss by enzymatic hydroylsis. The results were interpreted in terms of steric effect. Ester sulphate groups bound to external surfaces of soil humic polymers may be easily accessible to sulphatase enzyme and thus readily mineralizable during incubation or extraction of soil organic matter at low soluble-sulphate levels. Sulphate groups on inner surfaces of the organic polymers are shielded from the enzyme due to size exclusion and hence more stable.     

Active and passive organic matter fractions in Mediterranean forest soils

Soil organic carbon (C) is a complex set of pools, and to understand its dynamics it is necessary to know which of these pools are active at a given moment, and which act as passive, due to either physical protection or biochemical recalcitrance, or both. This matter has been studied mainly in agricultural soils. For forest soils, especially in Mediterranean areas, there is a data gap that needs to be filled. Therefore, we studied three profiles in Catalonia (NE Spain) over marl and under Pinus halepensis stands. Soil horizons were incubated under optimal conditions for 45 days. The respiration rate on day 45 was taken as basal respiration rate (BR_R). The following fractions were quantified: (1) soluble C, (2) microbial C, both corrected (MC_C) and uncorrected (MC_UC) (i.e., applying or not a correction factor to account for the non-extractable microbial carbon), (3) C in size fractions, isolated by ultrasonic dispersion and sieving plus sedimentation, and (4) labile and recalcitrant C, quantified by acid hydrolysis, applied to both the whole soil horizons and the size fractions. The basal respiration rate (BR_R) correlated best with the sum soluble + MC_UC, which altogether seem the best estimator of the active C pool. The correlation between BR_R and MC_C was worse, thus suggesting that not all microbial C should be included in the active pool. The correlation of BR_R with the C associated to coarse fractions (>50 μm) was positive, whereas that\with C associated to fine fractions (<20 μm) was negative. The correlations were lower than those obtained with the soluble + MC_UC, thus suggesting that the coarse organic fractions are probably the main source of active C, but not active C itself. Alone, the pools obtained by acid hydrolysis (labile and recalcitrant) correlated poorly with BR_R, but the combination of size fractionation with acid hydrolysis resulted in some of the best predictors of microbial activity. Hydrolyzable polyphenolic compounds inhibited microbial activity. Unhydrolyzable C associated to fine fractions (<20 μm) seemed the most stable of all the C pools studied. By contrast the unhydrolyzable part was apparently as unstable as the hydrolyzable part in the coarse organic debris. Overall, our results point to a hierarchy of constraints: both the physical protection and the biochemical quality affect microbial activity, but the physical protection goes first. In the profiles studied, C did not appear to be more stable in deep horizons than in surface horizons.     

Microbial biomass and organic matter turnover in wetland rice soils

A decline in rice yields has been associated with intensification of rice production. In continuously irrigated systems this has been attributed to a decline in soil N supply. Nutrient mineralisation and immobilisation is constrained by the quantity and nature of the organic substrates and the physico-chemical environment of the soil system itself. A flooded soil is very different from an aerobic one; electron acceptors other than oxygen have to be used. The transition to continuously anaerobic conditions associated with the intensification of wetland rice systems affects their organic matter turnover and may adversely affect their productivity.     

Soil organic matter in urban soils: Estimation of elemental carbon by thermal oxidation and characterization of organic matter by solid-state C nuclear magnetic resonance (NMR) spectroscopy

To reduce soil destruction by urban sprawl, land use planning has to promote the use of soils within cities. As soil functions are now protected by law in Germany, urban soil quality has to be evaluated before soil management. We studied contributions from elemental carbon (EC) and soil organic matter (SOM) quality in topsoil horizons at seven sites in Stuttgart, Germany, differing in impurities by technogenic substrates. The most disturbed site was found at a disused railway area while high-density areas, public parks and garden areas showed varying degrees of disturbance by anthropogenic activities. For most soils, compounds derived from plant litter dominated organic matter (OM) quality characterized by nuclear magnetic resonance (NMR) spectroscopy. Although high contents of EC (up to 70% of soil organic carbon) were indicated by thermal oxidation, this was not confirmed by aromatic C intensities in NMR spectra. Only for the highly aromatic railway soil were results for elemental carbon by thermal oxidation and NMR similar. As other technogenic substrates beside EC like plastics may also contribute in the long-term to OM in urban soils, new analytical techniques are therefore required. This knowledge will promote the evaluation of urban soil properties and their sustainable use.     

地中海山地土壤中团聚体的形成和有机质的储存

Soil aggregation and organic matter of soils from the pre-Pyrenean range in Catalonia (NE Spain) were studied, in order to assess their quality as carbon sinks and also to select the best soil management practices to preserve their quality. Aggregate stability, organic carbon and micromorphology were investigated. The highest amount of organic carbon was found in alluvial, deep soils (228 Mg C ha^-1), and the lowest was in a shallow, stony soil with a low plant cover (78 Mg C ha^-1). Subsurface horizons of degraded soils under pastures were the ones with smaller and less-stable aggregates. Fresh residues of organic matter (OM) were found mostly in interaggregate spaces. Within the aggregates there were some organic remains that were beginning to decompose, and also impregnative nodules of amorphous OM. Although OM was evenly distributed among the aggregate fractions, the larger blocky peds had more specific surface, contained less decomposed OM and had a lower organic/mineral interphase than smaller crumb aggregates, which were also more stable. Soil carbon storage was affected primarily by the OM inputs in the surface horizons. In order to store organic carbon over the mid-and long-term periods, the mechanisms favouring structuration through biological activity and creating small aggregates with intrapedal stable microporosities seemed to be the most effective.     

Hydrophobicity of organic matter in arable soils: influence of management

The affinity of soil organic matter for water influences resistance to microbial degradation, the rate of wetting and adsorption processes. Such properties play key roles in organic matter and microbial biomass dynamics, aggregate stability, water infiltration, leaching of organic and inorganic pollutants, chemical composition and the dynamics of dissolved organic matter (DOM). The hydrophobicity of the organic matter as a function of management have been studied in two soils with contrasting textures using diffuse reflectance infrared fourier transform spectroscopy (DRIFT). The results show that agricultural management clearly influences the amount of aliphatic C-H units and implicitly the hydrophobicity of the soil organic matter. A decrease of organic C due to management is accompanied by a decrease of hydrophobicity as well as of soil microbial activity and aggregate stability. The hydrophobicity index is a sensitive quantity to characterize the‘quality’ of soil organic matter. DRIFT spectroscopy proves to be a rapid and reliable technique to determine quantitatively the hydrophobicity of soil organic matter.     

Paramagnetic activity of organic matter in soils of the Ubsu-Nur Depression

The effect of the humus content and composition, the humification intensity, and the pH on the paramagnetic activity of organic matter in soils of vertical zones of the Ubsu-Nur Depression was revealed. It was found that the electron paramagnetic resonance (EPR) spectra of these soils have a relatively broad absorption band with the g factor equal to 2.0031 ± 0.0002; the EPR spectral curve has the form of the first derivative of the Gaussian absorption curve. The method of calculating the EPR spectral intensity was specified; regression equations were calculated for the pairs: the total carbon and the spectral intensity, the (HA + FA) carbon and the spectral intensity, and the C_ha/C_fa ratio and the spectral intensity, which showed a correlation between the group composition of the humus and the EPR spectral intensity. The results obtained permitted us to separate the soils of the Ubsu-Nur Depression into three groups with high, medium, and low effects of the humus status parameters on the EPR spectrum intensity.     

Influence of organic matter and pH on bentazone sorption in soils

Bentazone (3-isopropyl-1H-2,1,3-benzonthiadiazain-(4)3H-one 2,2-dioxide) is a postemergence herbicide which is used extensively worldwide, especially in China. The sorption of bentazone in various types of soils and extracted humic acids was investigated using a batch equilibration technique. Significant linearity was observed in sorption isotherms in five different types of soil, with distribution coefficients (K(d)) that varied between 0.140 and 0.321 mL g(-1). The distribution coefficient was determined to be a function of organic matter and pH in the soil. A model based on distribution coefficients was developed to predict bentazone sorption in soils. The organic matter-normalized partition coefficients for the neutral and anionic forms of bentazone were 370.3 and 2.40 mL g(-1), respectively. Hence, more attention should be given to the potential leaching problem when bentazone is applied in soils containing low organic matter and high pH.     

Detectability of degradable organic matter in agricultural soils by thermogravimetry

Sustainable agricultural land use requires an assessment of degradable soil organic matter (SOM) because of its key function for soil fertility and plant nutrition. Such an assessment for practical land use should consider transformation processes of SOM and its sources of different origin. In this study, we combined a 120‐day incubation experiment with thermal decay dynamics of agricultural soils altered by added organic amendments. The aim was to determine the abilities and limits of thermal analysis as a rapid approach revealing differences in the degradability of SOM. The carried out experiments based on two independent sampling sets. The first sample set consisted of soil samples taken from non‐fertilized plots of three German long‐term agricultural field experiments (LTAEs), then artificially mixed with straw, farmyard manure, sheep faeces, and charcoal equal to 60 Mg ha^?1 under laboratory conditions. The second sample set based on soil samples of different treatments (e.g., crop type, fertilization, cultivation) in LTAEs at Bad Lauchstädt and Müncheberg, Germany. Before and after the incubation experiment, thermal mass losses (TML) at selected temperatures were determined by thermogravimetry indicating the degradability of organic amendments mixed in soils. The results confirmed different microbial degradability of organic amendments and SOM under laboratory conditions. Thermal decay dynamics revealed incubation‐induced changes in the artificial soil mixtures primarily at TML around 300°C in the case of applied straw and sheep faeces, whereas farmyard manure showed mainly changes in TML around 450°C. Charcoal did not show significant degradation during incubation, which was confirmed by TML. Detailed analyses of the artificial soil mixtures revealed close correlations between CO₂‐C evolution during incubation and changes in TML at 300°C with R² > 0.96. Results of the soils from LTAEs showed similar incubation‐induced changes in thermal decay dynamics for fresh plant residues and farmyard manure. We conclude that the practical assessment of SOM could be facilitated by thermal decay dynamics if modified sample preparation and evaluation algorithms are used beyond traditional peak analysis.