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.     

Paleosol studies of burial mounds in the Ilovlya River valley (the Privolzhskaya Upland)

Paleosols buried under kurgans of the Bronze (end of the fourth and the third millennia BC), Early Iron (1st–3rd centuries AD), and Medieval (13th century AD) epochs have been studied on the Ilovlya River (a tributary of the Don River) terrace. The evolution of chestnut soils in the south of the Privolzhskaya Upland during the last 5000 years has been traced. It is shown that the mean weighted contents and distribution of soluble salts, gypsum, and carbonates in the soil profiles have been subjected to cyclic changes. The total microbial biomass and its trophic structure in the A1, B1, and B2k horizons of paleosols of different ages have been determined. A comparative analysis of the morphological, chemical, and microbiological data on the paleosols of different ages has been used to reconstruct the climatic dynamics for the last 50 centuries. The aridity of the climate in the studied region increased at the end of the third-the beginning of the second millennia BC and in the second and third centuries AD. The humidization of the climate took place in the 1st and in the 12th–13th centuries AD.     

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.     

Phosphatase activity in the surface and buried chestnut soils of the Volga-Don interfluve

The phosphatase activity (PA) was studied in the chestnut paleosols buried in 1718–1720 under the Anna Ivanovna rampart in the southern part of the Privolzhskaya Upland and in the middle of the third millennium BC under the burial mound of the Bronze Age on the Northern Yergeni Upland; the background analogues of these soils were also examined. The PA values in the fresh soil samples varied from 2.5 to 37 mg of P₂O₅/10 g of soil per h with maximums in the A1 horizon of the surface soils and in the B1 horizon of the paleosols. The PA values depended on the time of storage of the samples: with time, they increased by 2.6–2.9 times in the A1 horizon of the background surface soil and decreased by 20–60% in the other soil samples. The specific distribution patterns of the PA values in the soil profiles remained the same independently of the time of storage of the samples. Relatively small amounts of the soil samples were sufficient for the reliable determination of the PA: 1–2 g for the A1 horizon and 3–5 g for the B1 and B2 horizons. The time of incubation with the substrate had to be increased up to 4 h for the long-stored samples.     

Biological Activity of Brown Semidesert Soils of the Baer Knolls

Eurasian Soil Science - We have evaluated the biological activity of brown semidesert soils (Eutric Cambisols (Loamic, Protocalcic)) of the Baer Knolls (Astrakhan oblast) formed under different...     

Evolution of soils and dynamics of the climate of steppes in the southeast of the russian plain during the late eneolithic and bronze ages (fourth to second millennia BC)

On the basis of studies of subkurgan pedochronoseries, the main mechanisms of the development of soils of arid and desert steppes in drained landscapes of the southeastern Russian plain in the Late Eneolithic and Bronze ages (6000−3000 years ago) were established. During the fourth to third millennia BC, evolution of soils took place at the level of subtypes with a shift of boundaries of soil subzones toward the north. In each of the studied natural regions (Central Russian Upland, Volga Upland, Ergeni Hills, and Caspian Depression), an increase in the aridization of the climate in the second half of the third millennium BC can be distinctly traced, owing to which a convergence of the topsoil with the transformation of dark-chestnut, chestnut, and light-chestnut soils in chestnut-like semiarid soils, which dominated the region 4200–3900 years ago, occurred. In the first half of the second millennium BC, another change in the conditions of soil formation occurred that was caused by an increase in the degree of atmospheric humidity. It induced the divergence of the topsoil with a secondary formation of areas of zonal chestnut soils and solonetzes in place of chestnut-like soils by the middle of the second millennium BC. The obtained data gives reason to suggest that the age of modern chestnut solonetz complexes of the region does not exceed 3500 years.     

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.     

State of microbial communities in paleosols buried under kurgans of the desert-steppe zone in the Middle Bronze Age (27th–26th centuries BC) in relation to the dynamics of climate humidity

The size and structure of microbial pool in light chestnut paleosols and paleosolonetz buried under kurgans of the Middle Bronze Age 4600–4500 years ago (the burial mound heights are 45–173 cm), as well as in recent analogues in the desert-steppe zone (Western Ergeni, Salo-Manych Ridge), have been studied. In paleosol profiles, the living microbial biomass estimated from the content of phospholipids varies from 35 to 258% of the present-day value; the active biomass (responsive to glucose addition) in paleosols is 1?3 orders of magnitude lower than in recent analogues. The content of soil phospholipids is recalculated to that of microbial carbon, and its share in the total soil organic carbon is determined: it is 4.5–7.0% in recent soils and up to three times higher in the remained organic carbon of paleosols. The stability of microbial communities in the B1 horizon of paleosols is 1.3–2.2 times higher than in the upper horizon; in recent soils, it has a tendency to a decrease. The share of microorganisms feeding on plant residues in the ecological–trophic structure of paleosol microbial communities is higher by 23–35% and their index of oligotrophy is 3–5 times lower than in recent analogues. The size of microbial pool and its structure indicate a significantly higher input of plant residues into soils 4600–4500 years ago than in the recent time, which is related to the increase in atmospheric humidity in the studied zone. However, the occurrence depths of salt accumulations in profiles of the studied soils contradict this supposition. A short-term trend of increase in climate humidity is supposed, as indicated by microbial parameters (the most sensitive soil characteristics) or changes in the annual variation of precipitation (its increase in the warm season) during the construction of the mounds under study.     

Succession of Microbial Community in Gray Forest Soil during the Decomposition of Different Organic Compounds

Eurasian Soil Science - In a model laboratory experiment on gray forest soil, the succession of microbial communities during the decomposition of proteins, lipids, and polysaccharides was studied....     

Dynamics of the properties of steppe paleosols of the Sarmatian time (2nd century BC-4th century AD) in relation to secular variations in climatic humidity

Paleosols buried under kurgans of the Early (2nd-1st centuries BC), Middle (1st-2nd centuries AD) and Late (2nd-IV centuries AD) Sarmatian epochs were studied in dry steppes and desert steppes of the Lower Volga region (the Privolzhskaya and Ergeni Uplands and the Caspian Lowland). It was found that temporal variations in the morphological, chemical, microbiological, and magnetic properties of the paleosols in the interval of 2200–1600 BP were characterized by the cyclic pattern related to secular dynamics of climatic humidity with changes in the mean annual precipitation of ±30–50 mm. These climate changes did not transform chestnut paleosols and paleosolonetzes at the type or subtype taxonomic levels. However, they led to certain changes in the humus, carbonate, and salt profiles of the soils; in the character of solonetzic horizon B1; and in the state of microbial communities. According to these data, the Sarmatian time was characterized by alternation of micropluvial and microarid stages lasting fro about 100–200 years. In particular, the stages of humidization were observed in the 1st century BC-1st century AD and in the 4th century AD; the most arid conditions were observed in the second half of the 2nd and the first half of the 3rd century AD.