The microbial biomass in paleosols buried under kurgans and in recent soils in the steppe zone of the Lower Volga region

The total microbial biomass (TMB) was assessed in the chestnut and light chestnut soils and in the paleosols under burial mounds (steppe kurgans) in the Lower Volga region on the basis of data on the organic carbon content in the extracted microbial fraction supplemented with the data on the extraction completeness as a conversion coefficient. The completeness of the microbial fraction extraction was determined by direct counting of the microbial cells and colony-forming units (on plates with soil agar). The total microbial biomass varied from 400 to 6600 μg of C/soil. Its values in the buried soils were 3–5 times lower than those in the surface soils. The TMB distribution in the buried chestnut soil profile was close to that in its modern analogue (with the minimum in the B1 horizon). In the buried light chestnut paleosols, the TMB values usually increased down the profile; in the recent light chestnut soils, the maximum TMB values were found in the uppermost horizon.     

Characterization of the microbial communities in the modern and buried under kurgans soils of solonetzic complexes in the dry steppes of the Lower Volga region

The microbial communities were studied in the modern and buried under kurgans (1st century AD) soils of solonetzic complexes on the dry steppes of the northern part of the Yergeni Upland. It was found that the changes in the numbers of microorganisms from different trophic groups and in the biomass of the fungal mycelium along the profiles of the modern and buried solonetzic chestnut soils and solonetzes do not differ significantly. The quantitative estimate of the impact of the solonetzic process on the spatial variability of the microbiological parameters of the soils was given on the basis of the ANOVA. As a rule, the values of the microbiological parameters in all the horizons of the modern and buried chestnut soils were 1.2–2.8 times higher than those in the modern and buried solonetzes. The influence of the degree of solonetzicity of the buried paleosols on the microbiological parameters manifested itself in the entire profile, though in each particular horizon it was only seen in the numbers of some particular trophic groups of microorganisms. The comparison between the mean weighted values of the microbiological parameters in the entire soil profiles (the A1 + B1 + B2 horizons) demonstrated an inverse relationship between the population density of the microorganisms utilizing easily available organic matter and the degree of solonetzicity of the buried paleosols. The maximum biomass of the fungal mycelium was found in the solonetzic chestnut paleosol; it exceeded the biomass of the fungal mycelium in the other paleosols (which did not differ significantly in that parameter from one another) by 1.5–1.6 times.     

The morphology of cells and the biomass of microorganisms in the buried paleosols and modern steppe soils of the Lower Volga region

The morphology of microbial cells was studied, and the biomass of microorganisms was estimated in the modern steppe soils and paleosols buried under kurgans in the Lower Volga region with the methods of electron microscopy. The shape and ultrastructure of the cells in the modern soils and paleosols were similar, though their average volumes differed (0.37 and 0.28 μm³, respectively). The portion of cells with a volume above 1 μm³ in the surface soils and paleosols reached 10.9 and 9.2%, respectively, and the portion of cells with a volume less than 0.01 μm³ in the surface soils was 10% lower than that in the buried paleosols. It was found that the cells of the microorganisms have an external organomineral layer, which increases the cell volume by 4.9 times, and this fact was taken into account in the calculation of the microbial biomass. In the chestnut and light chestnut paleosols, the latter comprised 1500 and 230 μg of C/g soil, respectively.     

The biomass of fungal mycelium in buried paleosols and surface soils of the steppe zone

The contents of fungal mycelium have been studied in paleosols of ancient archeological monuments and in surface soils within the steppe, dry steppe, and desert zones of European Russia, on the Stavropol, Privolzhskaya, and Ergeni uplands. The buried paleosols date back to the Bronze Age (4600–4500 and 4000–3900 BP), the Early Iron Age (1900–1800 BP), and the early 18th century (1719–1721). The fungal mycelium has been found in all these paleosols. The biomass of fungal mycelium varies from 2 to 124 μg/g of soil. The distribution patterns of fungal mycelium in the profiles of buried paleosols and surface soils have been identified. It is shown that the dark-colored mycelium is typical of the ancient paleosols. In some cases, the content of the dark-colored mycelium in them may reach 100% of the total mycelium biomass.     

Paleosols buried under kurgans of the Pit-grave culture in the steppe zone of the Cis-Ural region

The analysis of soil chronosequences developed from loamy and loamy sandy substrates and buried under kurgans dating back to the Pit-grave archaeological culture in the steppe zone of the Cis-Ural region demonstrated that it is possible to trace the dynamics of the soil properties and to perform paleoclimatic reconstructions for different intervals within the studied period. The properties of sandy soils changed more rapidly than the properties of loamy soils. For sandy soils, notable changes in their properties were revealed in the soil chronosequences dating back to the particular stages of the Pit-grave culture; for loamy soils, such changes could only be traced for the soils buried under the kurgans dating back to different stages of the Pit-grave culture.     

The structural state of buried and surface soils of solonetzic complexes in the dry steppe zone of the Lower Volga basin

The structural state of modern (surface) soils and the soils buried under Anna Ioannovna??s rampart (1718?C1720) was studied. These soils are the components of solonetzic soil complexes in the southern Privolzhskaya Upland. The dehumification and the high content of calcium in the exchange complex determine the state of the macrostructure of the chestnut soil buried about 300 years ago. The dehumification drastically lowers the water stability of the soil aggregates, and the predominance of calcium ions in the soil exchange complex prevents the destruction of the chestnut paleosol aggregates and preserves their aggregate state upon moistening. For the last 300 years, no significant changes in the macrostructure of the solonetzes have been observed.     

Transformation of carbonate pedofeatures in paleosols buried under kurgans in the North Caucasus region

Carbonate concentrations in a chronosequence of paleosols buried under kurgans in the North Caucasus region at the end of the 4th century and the first half of the 5th century AD have been studied with the use of a set of morphological and isotopic methods. It is demonstrated that morphologically different phases of calcite—the collomorphic phase and the crystalline phase—in carbonate pedofeatures (calcareous pseudomycelium) and in the calcareous horizon have different elemental compositions and different isotopic compositions of carbon. Hence, these forms of calcite should have different origins. An addition of colloidal carbonates migrating in colloidal solutions from the lower soil horizons to the surface horizons during the periods of climatic aridization to the acicular calcite may be responsible for a sharp and irregular increase in the radiocarbon age of the newly formed carbonate pseudomycelium.     

Age and activation of microbial communities in soils under burial mounds and in recent surface soils of steppe zone

Chestnut paleosols buried under steppe kurgans about 4800, 4000, and 2000 years ago and their background analogues were studied in the dry steppe zone on the Volga-Don interfluve. Morphological, chemical, microbiological, biochemical, and radiocarbon studies were performed. Paleoclimatic conditions in the region were reconstructed on the basis of paleosol data. The ages of microbial fractions isolated from the buried and surface soils were determined using the method of ¹⁴C atomic mass-spectrometry. It reached 2100 years in the A1 horizon of the buried paleosol, which corresponded to the archaeological age of the kurgan (1st century AD). The ages of microbial biomass isolated from the B2 horizons of the buried paleosol and the background surface soil comprised 3680 ± 35 and 3300 ± 30 years, respectively. The obtained data confirmed our assumption about preservation of microorganisms of the past epochs in the paleosols buried under archaeological monuments. It is ensured by various mechanisms of adaptation of soil microbial communities to unfavorable environmental conditions (anabiosis, transformation of bacteria into nanoforms, etc.). The possibility to stimulate germination of the ancient dormant microbial pool isolated from the buried paleosols by 2–3 orders of magnitude with the use of β-indolyl-3-acetic acid as a signal substance was demonstrated.     

Modern and buried soils of kurgans in the forest-steppe zone of the Middle Volga region (by the example of Komintern I kurgan)

The construction of the Volga–Kama cascade of water reservoirs and hydroelectric power stations in the middle of the 20th century resulted in the inundation of vast areas and the development of abrasion along the shores that threatens many monuments of the archaeological and cultural heritage. The soils buried under northernmost kurgans of the Lugovskaya culture dating back to the 15th–14th centuries BC (kurgan Komintern I) were studied on the surface of the second terrace of the Kama River near its confluence with the Volga River. Burial sites of kurgan Komintern III were subjected to destruction in 1981, and archaeological excavations of kurgan Komintern II were performed in 2008. The danger of complete disappearance of these archaeological sites necessitated their thorough study with the use of multiple methods, including special paleosol studies. The soils buried under the kurgans ceased to be active components of the soil cover about 3500 years ago. They preserve information on the paleoenvironmental conditions before their burying. The analysis of morphological features and physical, physicochemical, and chemical properties of the buried soils attests to their chernozemic nature. Background surface soils that have passed through the entire cycle of the Holocene pedogenesis have evolved since that time into gray forest soils (Luvic Greyzemic Phaeozems) under forest vegetation. These soils are characterized by the increased acidity of the surface horizons (pH_КСl 4.3) and the development of lessivage. Data on the coefficients of mineral weathering in the buried paleosols and background surface soils attest to the identical precipitation both for the surface and buried soils in the Middle and Late Holocene.     

Mineralogical and chemical compositions of the paleosols of different ages buried under kurgans in the southern Ergeni region and their paleoclimatic interpretation

The chemical and mineralogical compositions and the contents and properties of the organic matter were studied in the paleosols of different ages buried under the kurgan group “Kalmykia” in the southern part of the Ergeni Upland. The investigated sequence of soils included profiles developed on the given territory about 5100, 4410, 4260, 4120, 3960, and 600 yrs ago. The background light chestnut soil was also examined. The results of our study showed that the earlier established climate changes in this area during the second half of the Holocene are reflected in the chemical and mineralogical compositions of the soils. These characteristics can be used as indicators of the paleoclimatic conditions together with some petrophysical characteristics, such as the magnetic susceptibility of the soil samples. The study of the mineralogical composition of the clay fraction of the paleosols attests to the transformation of the smectitic phase, accumulation of illites, and destruction of chlorites manifested at different degrees. It is argued that the geochemical indices—CIA, Al₂O₃/(CaO + MgO + K₂O + Na₂O), Rb/Sr, and Ba/Sr—are sensitive to climate changes and reflect the transformation of the mineral soil mass and the soil genesis.     

Paleosols of kurgans of the Early Iron Age in the Transural steppe zone

Paleosol studies of archaeological monuments of different ages have been conducted on the Transural Plateau. The morphological and physicochemical properties of paleosols under burial mounds (kurgans) of the Early Iron Age (the fifth and fourth centuries BC) were compared with the properties of background surface soils. A paleosol of the Savromat epoch (2500 BP) is characterized by high contents of gypsum and soluble salts. The presence of humus tongues in its profile attests to the aridity and continentality of the climatic conditions during that epoch. Paleosols buried under kurgans of the Late Sarmatian epoch and the Hun epoch (about 1600 BP) are characterized by a higher content of humus and greater depth of the carbonate horizon, which attests to the humidization of climatic conditions. The evolution of soils as related to climate dynamics in the first millennium BC and the first millennium AD is characterized.     

Assessment of the living and total biomass of microbial communities in the background chestnut soil and in the paleosols under burial mounds

The contents of phospholipids and carbon of the total microbial biomass were determined in the modern chestnut soil and in the paleosols buried under mounds of the Bronze and Early Iron Ages (5000–1800 years ago) in the dry steppe of the Lower Volga River basin. Judging from data on the ratio between the contents of phospholipids and organic carbon in the microbial cells, the carbon content of the living microbial biomass was calculated and compared with the total microbial biomass and total organic carbon in the studied soils. In the background chestnut soil, the content of phospholipids in the A1, B1, and B2 horizons amounted to 452, 205, and 189 nmol/g, respectively; in the paleosols, it was 28–130% of the present-day level. The maximum content was measured in the paleosols buried 5000 and 2000 years ago, in the periods with an increased humidity of the climate. In the background chestnut soil, the total microbial biomass was estimated at 5680 (the A1 horizon), 3380 (B1), and 4250 (B2) μg C/g; in the paleosols, it was by 2.5–7.0 times lower. In the upper horizons of the background soil, the portion of the living microbial biomass in the total biomass was much less than that in the paleosols under the burial mounds; it varied within 8.5–15.3% and 15–81%, respectively. The portion of living microbial biomass in the total organic carbon content of the background chestnut soil was about 4–8%. In the paleosols buried in the Early Iron Age (2000 and 1800 years ago), this value did not exceed 3–8%; in the paleosols of the Bronze Age (5000–4000 years ago), it reached 40% of the total organic carbon.     

The solonetzic process in surface soils and buried paleosols and its reflection in the mineralogical soil memory

The development of the solonetzic process in paleosols buried under kurgans and in the modern surface soils has been studied on the basis of the analysis of the clay (<1 μm) fraction. The revealed changes in the textural differentiation of the soils and the mineralogical composition of the clay fraction during 4500 years are assessed from the viewpoint of the “memory“ of the solid-phase soil components. The mineralogical characteristics show that the solonetzic process in the modern background soil is more developed. The mineralogical approach allows us to reveal the long-term changes in the soil status; it is less useful for studying the effect of short-term bioclimatic fluctuations. In the latter case, more labile soil characteristics should be used. The mineralogical method, combined with other methods, becomes more informative upon the study of soil chronosequences. Our studies have shown that the data on the clay minerals in the buried paleosols may contain specific information useful for paleoreconstructions that is not provided by other methods.     

Microbiological investigations of paleosols of archeological monuments in the steppe zone

Microbiological studies of the paleosols of archeological monuments (burial mounds) of the Neolithic, Bronze, Early Iron, and Middle Ages (the fourth millennium BC to the fourteenth century AD) located in the dry and desert steppe of the Lower Volga River basin were conducted. The microbial communities that existed at the time of creating the burial mounds were shown to be preserved up to the present time. This fact was confirmed by the regularities of the distribution of the microorganisms in the “mound-buried soil” system and by the data on the determination of the age for the microbial fraction of the paleosols using the method of ¹⁴C atomic mass spectrometry. The total biomass of the microbial communities in the paleosols amounted to 20–40% of the microbial biomass in their background analogues. In all the paleosols, a special pool of viable microorganisms was present. In the microbial community of the paleosols, the biomass of the active microorganisms corresponded to 0.30–41.0% of the biomass in the present-day soil; the content of mycelium of microscopic fungi composed 43–50% of that in the recent soil. In the mycelium structure in the paleosols, the share of the dark-colored mycelium increased to 98–100%. The microbiological parameters that give a contrasting characterization of the state of the microbial communities in the soils during the arid and humid climatic periods were revealed. The changes of the arid and humid climatic epochs were reflected in the structure of the microbial communities in the paleosols at the ecological-trophic, metabolic, and genetic levels.     

Physical, chemical, and mineralogical characteristics of steppe paleosols of the ural region

Investigation of paleosols with different ages of burial mounds and the unique fortified city of Arkhaim in the steppe zone of the Southern Trans-Urals (Chelyabinsk region) is carried out. They are located on the remnants of the Big Karaganka River valley. The time of construction of archaeological monuments dates back to the Early Iron Age (Sarmatian Culture, 2300–2200 years ago) and Middle Bronze Age (Sintashta culture, 3800–4100 years ago). The soils are of medium and light loamy granulometric composition. Morphological, chemical, and mineralogical investigations of paleosols and background soils indicate that, in the Sarmatian time, the climatic conditions in the region were drier than currently, while during the Sintashta cultural development, the climate of the region was similar to the present one.     

Production of CO<Subscript>2</Subscript> by surface and buried soils of the steppe zone under native and moistened conditions

Modern light chestnut and chestnut soils and their analogues buried under steppe kurgans in the southeastern part of the Russian Plain were studied in order to determine the rates of the CO₂ production by these soils under the native (with the natural moisture content) and moistened (60% of the total water capacity) conditions. It was found that the rates of the CO₂ production by the soil samples in the native state are relatively close to one another and vary from 0.3 to 1.4 μg of C/100 g of soil/h. The rates of the CO₂ production in the moistened state increased by two orders of magnitude for the modern surface soils and by an order of magnitude for the buried soils.     

Functional diversity of microbial communities in saline soils of the semidesert zone

The health status of microbial communities in soils of the Sulak Lowland (Dagestan) was estimated on the basis of data on their functional diversity. The health status of the microbial communities decreased in the following soil sequence: typical meadow soil > meadow-chestnut soil > dark chestnut soil > saline soil (solonchak). The low concentration of soluble salts (<1 meq/100 g of soil) had a positive effect on the functioning of the microbial communities. The health status of the microbial communities also depended on the soil humus content and pH conditions.     

Spatial variability of microbial communities in modern and buried soils of the Sakarka River Basin,the Privolzhskaya Upland

A comparative study of the microbial communities of the buried soils under the Anna Ioannovna mound (1718–1720) and the modern soils developed on different geomorphic positions (watershed, slope, and high floodplain) in the Sakarka River basin (the Privolzhskaya Upland) in the dry steppe zone was performed. The varying soil and ecological conditions of the different relief features were established to dictate the differences in the characteristics of the microbial community of the buried and modern soils, in particular, concerning the number of microorganisms belonging to different trophic groups (those restricted to sparse nutrients, humus-consuming ones, and those utilizing easily available organic matter), the ecologo-trophic structure, and the mycelia biomass and structure (the ratio between the light- and dark-colored hyphae). On the basis of the dispersion analysis, a qualitative estimation of the relief features’ impact on the spatial variations of the microbiological parameters of the soils under study is presented.     

Microbial communities of alluvial soils in the Volga River delta

The number and biomass of the microbial community in the upper humus horizon (0–20 cm) were determined in the main types of alluvial soils (mucky gley, desertified soddy calcareous, hydrometamorphic dark-humus soils) in the Volga River delta. Fungal mycelium and alga cells predominate in the biomass of the microorganisms (35–50% and 30–47%, respectively). The proportion of prokaryotes in the microbial biomass of the alluvial soils amounts to 2–6%. No significant seasonal dynamics in the number and biomass of microorganisms were revealed in the alluvial soils. The share of carbon of the microbial biomass in the total carbon content of the soil organic matter is 1.4–2.3% in the spring. High coefficients of microbial mineralization and oligotrophy characterize the processes of organic matter decomposition in the alluvial soils of the mucky gley, desertified soddy calcareous, and hydrometamorphic dark humus soil types.